The Natural Repertory of Prof. William Nelson

The Natural Repertory of Prof. William 

Nelson 

Edited by Professor Emeritus Desire’ Dubounet, IMUNE 

ISBN 978-615-5169-68-7 

1

The Natural Repertory 

Of 

Prof. William Nelson 

An In-Depth Understanding of 

Nelsonian Homeopathy 

Including a Catalogue of all two-hundred 

Nelsonian Homeopathic Remedies

The Natural Repertory of Prof. William Nelson 

© 1985, 1990 Academy of Applied Quantum 

Bio-Technologies. 

Rio Rancho, New Mexico 

Revised edition, 2008, William J. Cunningham 

White Dove Healing Arts, Ltd. 

All rights reserved. No part of this publication may be 

reproduced or transmitted in any form or by any means 

electronic or mechanical, including photocopying, 

recording, or any other information retrieval system, 

without permission in writing from: 

White Dove Healing Arts, Ltd. 

10959 Lynne Avenue, Lafayette, Colorado 80026 

Telephone (303) 828-4439

TABLE OF CONTENTS 

Introduction ______________________________________________________________________ 1 

Quantum Quality Control ~ QQC TM ___________________________________________________ 4 

Combination Homeopathy___________________________________________________________ 8 

Regarding the Remedies____________________________________________________________ 10 

Homeopathy______________________________________________________________________ 15 

Possible Mechanisms of Homeopathic Information Transfer________________________________ 22 

The Hormetic Philosophy___________________________________________________________ 29 

Nosodes_________________________________________________________________________ 34 

Isodes __________________________________________________________________________ 46 

The Liquitrophic Philosophy_________________________________________________________ 55 

The Anodyne Philosophy___________________________________________________________ 77 

The Combination Philosophy________________________________________________________ 83 

The Restorative Philosophy__________________________________________________________ 94 

Sarcodes ________________________________________________________________________ 96 

Oriental Herbal Philosophy__________________________________________________________ 106 

Chinese Herbology and Homeopathy__________________________________________________ 115 

The Miasm Philosophy_____________________________________________________________ 123 

The Psychological Philosophy________________________________________________________ 127 

Imponderable Homeopathy__________________________________________________________ 131 

Allersodes_______________________________________________________________________ 138 

The Dehabituate Philosophy_________________________________________________________ 157 

Vitamins and Powdered Products_____________________________________________________ 159 

Screening Groups Used in the Academy of Applied Quantum Biotechnology 

Computer Program_________________________________________________________________ 164 

List of Homeopathic Remedies with Similar Herbal Action_________________________________ 188 

An Advanced Treatise in Quantum Biology_____________________________________________ 198 

Alphabetical List of Health Disorders and Chromosome Locations___________________________ 214 

Lectins__________________________________________________________________________ 231 

Venoms_________________________________________________________________________ 239 

Gemmotherapy____________________________________________________________________ 259 

Classical Hahnemanian Singulars_____________________________________________________ 262 

A New Perspective on Research______________________________________________________ 264 

Metabolic Pathways _______________________________________________________________ 301

TABLES AND CHARTS 

Periodic Table – Crystal Structure______________________________________________ 12 

Duplication Study__________________________________________________________ 25 

Comparison Chart: New Homeopathy – Allopathy________________________________ 26 

Inflammation: Part of the Defense Phase of Life__________________________________ 27 

Chromosome Homeopathic___________________________________________________ 230 

Snake Venoms Containing NGF_______________________________________________ 245 

Distribution of Hemorrhagic, Lethal and Proteolytic Activities in Snake Venoms________ 247 

Effect of Venoms from Different Species of Snakes on the Histamine (H) and Serotonin (S) 

Content of Isolated Rabbit Platelets_____________________________________________ 248 

Summary of Immunopathology, Histopathology, and Electro-microscopic findings of the 

Kidney in Snakebite_________________________________________________________ 254 

Renal Failure with Known Lesions in Various Snakebites___________________________ 255

First, do no harm 

DR. RECOMMENDS’ PLEDGE 

� We pledge to provide safe products and to educate practitioners in 

understanding their efficacy and using them safely. 

Help ease misery and suffering 

� We pledge to test and develop the highest quality products, and to 

educate practitioners in relieving causes of disease and to 

stimulate recovery. 

Respect the natural process of God’s living world 

� We pledge to remember that we do not know and that nature does 

know, thus, we shall use as natural a healing process as possible. 

Provide research, consulting and education in natural, homeopathic and 

nutritional healing 

� We pledge to broaden confidence through the realization that 

natural healing methods are superior to synthetic ones in the long 

run and often in the short term. 

***

INTRODUCTION 

A repertory is a compilation of the homeopathics used by a 

practitioner, and many have been written by homeopaths throughout the 

ages. This particular one is the Natural Repertory of Dr. William Nelson. 

With this book, homeopathy enters into the modern age in regard to 

toxicity, hormones, amino acids, minerals, vitamins, sarcodes, nosodes, 

allersodes, isodes, and classical homeopathy. This is by far, to date, the 

most extensive repertory ever compiled by any homeopath. 

Within these pages, there are many remedies that are used for the 

entire human condition. For every known disease, we have developed 

nosodes, sarcodes, isodes, allersodes, and classical treatments. Within 

this document, we propose a new vision of statistical analysis that will 

modernize homeopathy and bring it into the new age of modern 

medicine. 

We also offer a new definition of homeopathy here, one that is broader; 

from reversal (which is not apropos to all of homeopathy) to herbology, 

naturopathy, and all forms of natural medicine. Our new definition will 

show how homeopathy is the science of using the body to respond, 

rather than using external means, which is the philosophy of allopathy. 

Allopathy tries to artificially reduce symptoms, which can sometimes 

make the patient dependent on an external agent. In homeopathy, it is 

about working with a natural entity to try to balance the patient’s 

metabolism. At times, allopathy is used but only in its most gentle form 

in trying to stimulate the body to achieve balance by itself. We can fight 

symptoms allopathically while trying to produce harmony and natural 

health in the patient. Homeopathy is equivalent to system balance, and 

allopathy implies an external treatment of the symptoms. 

Within these pages, we present a new era of homeopathy, a new era of 

understanding and expansion of homeopathy from its limited confines to 

a broader based, total m edical system. 

1

Many classic homeopaths may not completely understand everything 

within this treatise. They may struggle and try to rationalize against 

using the remedies. We only can hope that they will embrace the vision 

and understand how homeopathy can be used in dramatic, new ways. 

We feel history is being expanded within these pages, allowing the 

homeopath to broaden their base of understanding to encompass the 

total concept of biology and medicine. 

We welcome the open-minded reader to this exciting, new concept of 

homeopathic thinking. 

2

Protocol for Wellness 

� Relieve or diminish the causes of disease as much as possible, and 

improve on one’s lifestyle. 

� Treat the organs of involvement by rebuilding, draining, de-toxing, 

and reconstructing. Use sarcodes (glandulars) and the correct 

structure and flow. 

� Re-establish the balance of flow through adjustment, yoga, 

acupuncture, acupressure, electric field work, polarity techniques, 

etc. 

� Relieve symptoms by balancing homeostasis through homeopathy. 

The use of combination homeopathics makes it safe and easy. 

� Use nutrition, exercise, affirmation, massage, and stress reduction 

programs. 

Our next challenge concerns the politics of free choice. We need to 

develop a safe system in which we can train and watch over these 

different wellness consultants, and to encourage the people of the United 

States to freely choose wellness intervention over crisis intervention. 

3

Quantum Quality Control ~ QQC TM 

Quantum Quality Control or Double QC (QQC TM ) is a trademark of Dr. 

Nelson’s, developed by him to determine the finest quality control that 

can be utilized in the development of homeopathics. Walter Shewhart 

came up with the idea of superb quality control as the hallmark of a good 

business that would last through financial difficulties. He offered this 

technology to the Americans in the 1950s and early 60s, and American 

industry scoffed at him. W. Edward Deming collaborated with Shewhart 

and when the boom markets were not interested in incentives for quality, 

he eventually left America and found a welcome home in the Japanese 

market where quality control became the pinnacle of Japanese 

businesses. This helped the small nation which was recovering after the 

devastation of the World War to become a new economic power 

dominating the car market and electronics industries as well as many 

others through the utilization of quality control. 

Many surmise that purchases from the Orient are junk but these are 

rarely from Japan; more often they are from Taiwan or Hong Kong. The 

Japanese try to excel in quality control and make it a hallmark of their 

industry. Quality is the best way to build a business and quality control 

is the best tool. Using this model, we try to develop a quality control 

technique for homeopathy that would allow us to produce the finest 

homeopathic products. 

A complete description of this double QC process is included in the 

Quantum Vibrational Medicine of Dr. Nelson, in which the analysis of the 

different techniques and how they came about are explained. We go into 

the magnetic, static and conductance patterns and the trivector fields 

produced by bio-quantum homeopathics, and we explain the logical 

capacities of these homeopathics. Looking at the polymorphic state or 

liquid crystal effect is also well discussed in the book. 

4

We wish to briefly discuss quality control to help doctors understand 

how Dr. Recommends can develop the finest homeopathics in the world. 

Many techniques are used, including superb intake or initial acceptance 

criteria to allow only the finest quality herb, hormone, enzyme, sarcode, 

nosode, isode or allersode. This way there is control each step of the 

process through the shape, structure, electrodynamics, Kirlian 

photography, and other dramatic means. Below are some profiles used to 

develop this QQC TM process. 

The QQC TM process includes developing the best statistical information 

on the product in a clinical setting, to make sure that the products not 

only fit our QQC TM process but also work in patient populations, 

guaranteeing safety and efficacy. 

Dr. Recommends has developed the finest in homeopathy, as well as 

the most extensive remedy list in the industry today. With these different 

compounds we have the finest medical pharmaceutical house in the 

world for the widest variety of ailments. We insist on: 

� Statistical evaluation of clinical results to confirm safety and 

efficacy 

� Raw material intake must begin with the best 

� Kirlian photography to confirm bio-energy field stability 

� Trivector analysis to confirm polymorphic liquid crystal state 

� Cryogenic photography to confirm polymorphic liquid crystal state 

� Spectro-photometry and atomic absorption to confirm bio-photon 

absorption and release 

� Culture to confirm safety 

� Chromatography to confirm safety 

� Pro bono programs to give back by helping the poor 

� Education for the doctor and the public 

5

On the first page is the Dr. Recommends’ pledge which includes safety 

first, then efficacy. We revere nature in all that we do even though we 

realize that sometimes we must use synthetic pharmaceuticals to break 

up the damage done before. We revere the natural process in every way 

possible. 

We also provide education. A repertory can only outline products, and 

not really spell out their use. To obtain more information the reader is 

pointed to a list of books by Dr. Nelson that can be found at 

http://www.whitedovehealing.com/training/books.htm. (White Dove 

Healing Arts, Ltd.) Many of these books are on video and audio tape, 

which will help the practitioner with the wide range of health issues and 

encourage the use of some of these simple homeopathic techniques thus 

increasing cure rate, and helping patients in many new ways. It is hoped 

that these books offer data needed to continue broadening the ability to 

cure, so that diseases on earth can be a thing of the past by helping to 

provide simple, natural, safe, medical solutions. 

These techniques are utilized only by Dr. Recommends for quality 

control management to develop the finest homeopathics. Only by using 

the finest quality products can homeopaths truly succeed. The people of 

the world want natural medicines and a medical philosophy that works 

with the body, not against it. Homeopaths now need to maximize their 

results and can do so if the industry will focus on quality. 

The Dr. Recommends’ Quantum Quality Control consists of 

spectrophotometry and atomic absorption, electrolyte potential, Kirlian 

field analysis, bacteria and fungal cultures, rickettsia and viral detection, 

trivector analysis, cryogenic photography, and pilot and clinical testing. 

This thorough policy of product control provides the quality of product 

that everyone deserves. 

Double QC is the process of quality control which will assure the finest 

energetic remedies. The Nelsonian manufacturing process gives a more 

active homeopathic. Sea life, brain hormones, and enzymes are mixed 

6

into each batch and an electrical potential current is run through the 

base alcohol and water to produce the finest homeopathics in the world. 

The eight steps in Quantum Quality Control ~ QQC TM 

� Raw materials intake (make sure you begin with the best) 

� Kirlian photography (confirm bio-energy field stability) 

� Trivector analysis (confirm electronic, magnetic, capacitance state) 

� Cryogenic photography (confirm polymorphic liquid crystal state) 

� Spectrophotometry and atomic absorption (confirm bio-photon 

absorption and release) 

� Culture (confirm safety – no micro-organism growth) 

� Chromatography (confirm safety – proper protein, hormone and 

enzyme existence) 

� Statistical evaluation of clinical results (confirm safety and efficacy) 

7

Combination Homeopathy 

Classic homeopathy uses singular compounds in their basic form 

which were devised by Samuel Hahnemann. Hahnemann never realized 

the important fact that all the compounds he was using were 

combinations of many other compounds and elements. Apis mellifica is a 

very complex combination that nature has developed into a single energy 

pattern. There are over 50,000 known compounds in this singular 

remedy. 

The very principle of nature is combination in which many elements 

are blended into life. If we were to blend Apis mellifica with Lachesis, two 

biological compounds, we would get a new entity unlike each of them 

separately. Their effects might be amplified, cancelled or synergistically 

changed. The skill is to treat the combination as a new entity that needs 

scientific validation. 

Combination homeopathy involves one to blend or prepare different 

remedies for broader based action which most classic homeopathic 

combinations are used for. For just one patient we might take a specific 

group of allergens, isodes, nosodes, or sarcodes and combine them in a 

way that produces a combination specifically for the patient. The 

scientific art in combination homeopathy is covered in Quantum 

Vibrational Medicine. 

Much of combination homeopathy was developed to make the 

principles of homeopathy easy for practitioners to use. With combination 

homeopathy, doctors no longer have to remember the profile of each 

individual entity. They can remember simple terms such as “pain, heat 

improves” or “pain, cold improves.” The practitioner only has to know two 

different concepts in the face of pain; heat and cold. 

Combination homeopathy offers safety as well as an increased band of 

efficacy over most singular homeopathics. The argument for combination 

homeopathy includes several justifiable concepts that most singular 

8

homeopaths may not truly know about. Most singular homeopaths argue 

circularly, and may never have tried combinations because they have 

superstitious or vague beliefs that only Hahnemann truly understood 

homeopathy, not even considering the fact that the world has changed 

dramatically since his time. This belief is often fostered by minds that 

resist new thinking and scientific improvements. This way of thinking 

and lack of science has held homeopathy back long enough. 

Dr. Nelson has devised many combination homeopathics that are easy 

to use by practitioners. These homeopathics are tested in statistical 

ways. If we look into the chapter called “A New Perspective on Research,” 

in Bio-Quantum Matrix, we can read some new statistical information that 

will prove the safety and efficacy of such formulas. In The Experimental 

Data on Homeopathy clinical tests validate results that prove 

homeopathy’s effectiveness. These many combinations teach homeopaths 

to use homeopathy in broader ways. 

Combination homeopathy offers the best techniques to entice 

allopathic medical doctors into the homeopathic camp as it can be 

taught very quickly and easily. A list of the many different combination 

remedies used by Dr. Recommends is included here. It goes way beyond 

homeopathic lines that existed before. 

We welcome the reader and practitioner to a new world of homeopathy 

and a deep understanding of how to utilize the combinations more 

significantly. 

After presenting this list, different types of remedies used for 

circulation, nerve disorders, digestion problems, immunology, and other 

types of sicknesses will be covered. This will allow the practitioner some 

viable shortcuts in using homeopathy. 

9

Regarding the Remedies 

The Dr. Recommends’ combination remedies are developed with several 

advantageous points in mind. They are as follows: 

� Ease of use: Designed for the busy doctor to learn about and use. 

� Guaranteed safety: Engineered to be safe – first don’t hurt. 

� Effectiveness: Passed crucial quantum quality control procedures 

that surpass other homeopathics in the world. 

� Affordable: Easily affordable. 

� High quality service: Delivery on special order items beats most 

regular deliver. 

� FDA registered: Registered with the FDA (National Drug Code/ 

NDC numbers) and are also registered in Canada (Drug 

Identification Number/DIN), Australia, and the Common Market. 

� World wide distribution. 

This catalog contains the most dramatic homeopathic remedies ever 

engineered. The Dr. Recommends’ remedies are scientifically formulated 

and contain many trace elements from the Polymorphic Periodic Table 

developed by Dr. James Isaacs. Trace elements have profound biological 

effects by producing stimulating and stabilizing effects on the body. 

Trace element therapies are used in conjunction with scientifically 

developed sarcodes, nosodes and isodes. The shape and atomic structure 

of these elements are used in making the Dr. Recommends’ remedies the 

most effective homeopathics in the world. 

Dr. Recommends’ remedies use very high potencies, along with lower 

potencies, in a homochord blend. This unique, scientific combining of the 

homochords guarantee their safety and effectiveness. To ensure the 

quality of the product, Dr. Recommends’ remedies are quantum quality 

10

controlled using the QQC TM techniques. This produces the finest and 

most profound healing combinations. Dr. Recommends’ remedies are 

made with the Nelsonian manufacturing process which activates 

electrical, synergistic, polymorphic and energetic potentials. 

Unfortunately, the Nelsonian process increases the energy so well that 

electronic duplicators and imprinters cannot duplicate these formulas. 

The Dr. Recommends’ remedies are designed to blend with each other 

and work together for health. Any contraindication to the mixing of these 

remedies will be noted. These remedies are safe and easy to use. 

11

Periodic Table – Crystal Structure 

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 

H He 

1 

Hex 

Hex 

Li Be B C N O F Ne 

2 Cub Hex Rhom Hex Hex Cub Cub Cub 

Na Mg Al Si P S Cl Ar 

3 

Cub Hex 

Cub Cub Mono Ortho Ortho Cub 

K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr 

4 Cub Cub Hex Hex Cub Cub Cub Cub Hex Cub Cub Hex Ortho Cub Rhom Hex Ortho Cub 

Rb Sr Y Zr Nb Mo Tc Ru Rh Pd Ag Cd In Sn Sb Te I Xe 

5 Cub Cub Hex Hex Cub Cub Hex Hex Cub Cub Cub Hex Tet Tet Rhom Hex Ortho Cub 

Cs Ba * Hf Ta W Re Os Ir Pt Au Hg Tl Pb Bi Po At Rn 

6 Cub Cub Hex Cub Cub Hex Hex Cub Cub Cub Rhom Hex Cub Rhom Mono ? Cub 

Fr Ra ** Rf Db Sg Bh Hs Mt Uun Uuu Uub 

7 Cub Cub ? ? ? ? ? ? ? ? ? 

* La Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu 

Hex Cub Hex Hex Hex Rhom Cub Hex Hex Hex Hex Hex Hex Cub Hex 

** Ac Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr 

Cub Cub Ortho Ortho Ortho Mono Hex ? ? ? ? ? ? ? ? 

Crystal Structure Abbreviations 

Hex Hexagonal 

Rhom Rhombohedral 

Cub Cubic 

Mono Monoclinic 

Ortho Orthorhombic 

Tet Tetragonal 

? Unknown 

http://www.chemicalelements.com/show/crystalstructure.html 

12

HOW THE COMBINATION REMEDIES ARE USED 

� Homeopathy can be used as nutritional supplementation. If we use 

a homeopathic compound such as Vitamin B to supplement the 

body’s deficiency syndrome, then homeopathy is used in a 

nutritional sense. A concentrated source of B-12 which is diluted, 

one part to ten, six times, arrives at a 6x. This is approximately 

equal to the RDA of B12, 5 micrograms. Homeopathic remedies 

made for nutritional supplementation can be found in the 

Liquitrophics and Vitamin sections. Vitamins in the minimal dose 

can also be used to regulate metabolism of the vitamins. The 

theories of Dr. Royal Lee, the Father of Natural Vitamins, proved 

that low doses of natural, high quality vitamins can do the job 

better than mega dose, synthetic vitamins. 

� Homeopathy can be used to help stimulate the body. If a low dose 

homeopathic of Belladonna is used, it is possible to achieve the 

low-dose pharmacological action. This will trigger the body to 

stimulate its own healing. The vast difference between homeopathy 

and allopathy is that homeopathy does not incur dependence, but 

rather uses the minimal dose philosophy and gently shifts the 

patient towards restoring health. Homeopathy stimulates the body 

where allopathy works against the symptoms. 

� Homeopathy can be used in classic ways to help reverse 

symptoms. Homeopathy can help reverse symptoms and stimulate 

the body to return to the balance of its cybernetic systems. 

Homeopathy encourages homeostasis and cure without side 

effects. In homeopathy, the symptoms are messengers of 

underlying imbalances; whereas allopathy works in synthetic ways 

to only control symptoms. 

� Homeopathy works to encourage energetic stabilization. 

Homeopathy encourages energetic stabilization by encouraging 

13

correct tissue development with sarcodes, reducing allergic 

reactivity with allersodes, increasing hormetic detox with nosodes, 

stabilizing synthetic reactions with isodes and producing healing 

effects with imponderables and classic remedies. 

Classification of the Remedies 

Dr. Recommends’ remedies are classified in the following manner: 

� Over the counter (OTC). This category does not require a 

prescription from a medical doctor. It is sold to the public and it is 

safe to use. It does not require professional training to be obtained. 

� Professional Use. This category includes such practitioners as 

licensed naturopaths, massage therapists, or other professionals 

who do not have a license to dispense pharmaceuticals. 

� Rx. The remedies in this category can only be prescribed by a 

licensed medical professional within the states. 

14

Homeopathy 

The theory and practice of homeopathy is strange to those of us who 

are accustomed to conventional Western medicine. But we all sense the 

rightness of a healing system which conceives of all symptoms as parts of 

a larger whole, which appears to stimulate the body’s natural healing 

force rather than attack its parts. Homeopathy seems to work with us, 

not on us. It assists our innate biological intelligence to be healthy. When 

we break a bone, it is our innate intelligence that repairs it. In fact, our 

bodies can heal themselves of dramatic diseases. Homeopathy 

encourages and maximizes our innate intelligence to cure ourselves. 

At one time, homeopathy was the number one form of medicine in the 

United States. Allopathy rose to precedence when the culture turned 

towards the economically driven development of synthetic chemicals and 

turned its back on natural healing techniques. Now homeopathy is 

experiencing regeneration in the United States. The rise in iatrogenic 

diseases and synthetic chemical problems has reintroduced the 

importance of choosing natural healing techniques. 

Homeopathy is the science of healing from within, or prompting the 

organism to heal itself. Homeopathics are used to stimulate the organism 

toward its own state of homeostasis (balance). Homeopathy is a concept 

of minimal dose which Samuel Hahnemann, the Father of Homeopathy, 

discovered while trying to determine the smallest amount of a 

pharmacological agent that could gently nudge the patient back into the 

biological cybernetics of health. Using a “feather” to stimulate such a 

balance is the principle of homeopathy. 

Throughout history, disease has been viewed from two fundamentally 

different perspectives: One, as a malfunction of specific components of 

the body, where symptoms are seen as the disease itself, and two, where 

symptoms are a result of a deeper disturbance or imbalance of the 

person as a whole, and where symptoms are simply the outward 

15

manifestation. Disease is the blockage of the flow of life, and symptoms 

are the body’s way of dealing with the blockage. Symptoms just point the 

way towards natural homeostasis and homeopathic cure. 

Perspective number one is the basis underlying modern orthodox 

medicine. Whatever symptoms arise, they are counteracted by drugs, 

e.g., an antihistamine for a histamine reaction, an analgesic for pain, 

steroids for inflammation, an MAO inhibitor for depression, an 

antipyretic for fever, etc. In allopathy, 95 percent of all pharmacology 

works against symptoms and against the body. However, perspective 

number two is an ancient concept which underlies the entire holistic 

health movement, including homeopathy. Nature is revered and utilized 

to balance the system. The innate intelligence is worked with, not 

against. With homeopathy, side effects are relatively unknown. 

Symptoms are not the disease, they merely accompany the disease. 

Symptoms are evidence of disease. But treating symptoms is like killing 

the messenger for bringing bad news. In fact, by treating symptoms you 

are suppressing the body’s natural responses and inhibiting the healing 

process, interfering with life. 

As far back as 190 years ago, long before the term “holistic health” was 

coined, homeopaths recognized the inseparability of body and mind. 

Homeopaths have always stressed the importance of assessing the 

totality of the person. Homeopathic medicines thus have physiological 

activity. Violinist Yehudi Menuhin once said, “Homeopathy is one of the 

rare medical approaches which carries no penalties – only benefits.” In 

theory, there is no reason why orthodox medicine should not embrace 

homeopathy as an ally. 

16

Significance of Homeopathy 

There is a growing consensus in the world that the massive 

expenditures on medical research have failed to demonstrate any 

significant improvement in society’s level of health. The incidence of 

major chronic diseases like cancer, diabetes and heart disease has 

continued to climb, and medical costs have soared beyond the means of 

the average person. More and more, doctors and lay people alike are 

searching for alternatives. 

Homeopathy offers a time tested method which satisfies the need for a 

more economical and non-toxic therapy. It encompasses all areas of 

medical care – prevention, emergency and acute care, and chronic 

disease treatment. Homeopathy offers the individual and society 

improved health, productivity, and enjoyment of life. 

17

Advantages of Combination Homeopathic Therapy 

� Combination homeopathic remedies are safe, effective and 

compatible with all types of medical, surgical, psychological, 

physical and nutritional therapies. 

� Homeopathy is the safest method for treating infants, children, 

elderly patients and individuals who have an allergic history of 

drug reaction. 

� Combination homeopathic remedies provide a wider range of 

utility. 

� Combination homeopathics offer increased safety due to fewer side 

effects. 

� Iatrogenic or toxic reactions are rare. 

� Fatal poisoning is unheard of. 

� Recovery is usually progressive. 

� Disorders for which no specific medication is available may 

respond to homeopathics. 

� Homeopathy can rescue the medical establishment from its drug 

addiction. 

� The expense is minimal. 

� Homeopathy stimulates the body into a healing process – it goes 

beyond just treating the symptoms. 

� Combination homeopathy is easy to learn and to use. 

18

We have: 

AMERICA IS PREPARED MEDICALLY FOR EVERYTHING 

The most hospitals 

The most drug stores 

The most pharmacists 

The most nursing homes 

The most medical doctors 

The most medical schools 

The most surgical operations 

The most clinical laboratories 

The most nurses and nurses’ aides 

The most education about disease 

The most publicity about diseases 

The most “sick” insurance policies 

The most medical scientific research 

The most pharmaceutical companies 

The most “sick” insurance companies 

The most physician office laboratories 

The most medical research in the world 

The most health societies and associations 

The most radio and television “sick” talk about disease 

The most federal government medical agencies 

A USDA, FDA, HCFA, CDC AND SURGEON GENERAL 

The most State and local health agencies 

WITH 

THE WORLDS’S HIGHEST MEDICAL COSTS 

EVERYTHING BUT GOOD HEALTH 

“Any serious proposal that is genuinely designed to prevent disease 

will be sure to meet with stubborn opposition from those who have a 

vested interest in disease. Prevention, if genuine, would put the 

disease treaters out of business. Without the sick man the entire 

medical industry would collapse, consequently, it becomes necessary 

that there shall always be a sick man.” - Herbert Sheldon 

BUT IT DOESN’T’ HAVE TO BE. 

19

PREVENTION OF DISEASE 

Every person can prevent disease. Every person can attract disease. 

The list of diseases below can create more suffering and affect more 

lives and more people than earthquakes, floods or other natural 

disasters in the United States. Yet man devotes more time and money 

to control natural disasters than to prevent disease. 

The cause for most of the non-infectious diseases listed below can 

be food related. 

One does not have to be 

� One of the 1 million who will be diagnosed with cancer this 

year 

� One of the 1 million who die of cancer each year. 

� One of the 1 million who die of heart disease 

� One of the 400,000 new cases of skin cancer each year. 

� One of the 126,000 new cases of colon cancer each year. 

� One of the 99,000 new cases of uterine cancer each year. 

� One of the 38,000 new cases of bladder cancer each year. 

� One of the 45 million who suffer headaches. 

� One of the 35 million who suffer from allergy. 

� One of the 7 million who have coronary artery disease. 

� One of the 37 million who suffer from hypertension. 

� One of the 9 million who suffer from asthma. 

� One of the 1.6 million suffering from gout. 

� One of the 100 million who suffer from chronic back pain. 

� One of the 36 million who suffer from hearing loss. 

� One of the 24.5 million who have cataracts. 

� One of the 26 million who suffer from gallstones. 

� One of the 6.5 million who suffer from osteoporosis. 

� One of the 225,000 to undergo angioplasty. 

� One of the 35 million to suffer from candidiasis. 

� One of the 35 million to undergo surgery each year. 

� One of 36 million who can’t afford ‘sick’ insurance. 

� One of the 6.9 million currently confined to a nursing home 

for long term nursing care. The projection for the year 2040 

is 18 million. 

20

Dangers of Homeopathic Utilization 

� Masking a major disorder: This may provoke a patient to not 

seek proper medical care. If symptoms persist, seek medical 

attention; always work with a doctor’s supervision for maximum 

safety. Try to choose a physician who is reverent of nature and 

reluctant to use synthetics. 

� Alcohol sensitivities: If alcohol sensitive, the homeopathic drops 

may be put into a 3 oz. glass of warm water. Allow 1 minute for 

alcohol to evaporate. If the problem persists, alcohol sensitive 

persons may get remedies in pills without alcohol. 

� Provings: This is a symptom caused by a homeopathic, and it is 

usually mild in appearance. If the homeopathic is terminated 

and symptoms abate in 24 hours, it could be a proving; if 

symptoms continue after 24 hours, then it is unlikely they were 

caused by the homeopathic. It is natural for modest symptoms 

to be exhibited during the healing and cleansing of the body. 

When symptoms grow in intensity or for a prolonged length of 

time seek professional help. 

The Food and Drug Administration (FDA) recognizes the 

Homeopathic Pharmacopoeia of the United States (HPUS) regulations, 

which indicate how remedies should be made, dispensed and utilized 

by homeopathic practitioners. The remedies in this catalog are 

registered with the FDA, following HPUS guidelines. 

21

POSSIBLE MECHANISMS OF HOMEOPATHIC 

INFORMATION TRANSFER 

Homeopathy is a medical art used for centuries to treat illness. But 

what are the ways in which a homeopathic can work? Please see the 

list below: 

� Pharmacology: Low potency products which in dilute form 

follow two laws: 

Arundt-Schultz Law – A very small dose of a poison has 

reverse effects of the larger mega dose, i.e., homeopathic 

belladonna relieves the redness and dryness that raw 

belladonna produces. 

Law of Initial Values – As the quantity of substance is 

proportionately reduced the potent effectiveness can elevate, 

paradoxically reverse, or reduce depending on the substance 

itself. 

� Imprinting of a message into the polymorphic structure of the 

carrier water and alcohol mixture. Here the clath-rate structure 

of water is changed to receive a message and transfer this 

message to a patient. The receptors for this message would be 

on the cell membrane and be similar to olfactory receptors of 

the nose. This might explain the ability of strong odors to block 

homeopathy. 

� Quantic storage of information in the quantic states of the 

electrons, atoms, and molecules of the carrier fluid. This 

transfer would be disrupted by sunlight, x-ray, or other photon 

or particle release. Homeopathics are sensitive to the same. 

Energy is needed for this shift and possibly could be supplied 

by succussion. (There seems to be a minimum of times a 

product needs to be succussed: 10 to 15 times). 

22

� Energetic and electrical pattern of the homeopathic. By 

analyzing the spectral reactions of the homeopathic to 

conductance, electrons, inductance (magnetic relativity), and 

capacitance (static reactance). This gives a trivector analysis of 

the electrical signature of the homeopathic. 

� Storage might take place in dimensions beyond the 1 st , 2 nd , 3 rd , 

and 4 th . Some shift of matter in dimensions 4, 5, and 6 might 

be a possible place for memory storage of a homeopathic. This 

might explain the imponderables of homeopathy or the power of 

energy healing. This is measured by correlating the virtual 

biophotons of a homeopathic. 

In the second mode, the memory ability of water and alcohol is 

mentioned. This phenomena can be studied through photon scattering 

tests, nuclear magnetic resonance and simplest of all, freezing. If the 

water holds a plastic amorphous memory in liquid form as it enters solid 

form, this shape should have some effect on the ice patterns. A freezer 

that maintains -5c within 1 degree was used to crystallize the 

substances. The homeopathics used were less than 5% alcohol to allow 

proper freezing. They were put into 1 in. circular 1/8 in. deep trays, and 

then allowed to cool in the refrigerator for 2 hours at +5c before insertion 

into the freezer at -5c. After 12 hours, the disks were frozen and allowed 

investigation. Patterns would form on the homeopathics. There was 

indeed some shape transfer even beyond 25x where probabilities of 

product existing are minuscule. 

Another easy way to measure energetic homeopathics is through 

Kirlian photography. This involves simply placing the product in a highly 

charged electrical field through a container or rare electron gasses. The 

electric charge fluoresces the gas, but the homeopathic acts as a prism to 

direct the charge and each homeopathic produces its own fingerprint or 

pattern of colors to identify it. These charged particles will be enhanced 

23

y the polymorphic shape of the water, the quantic states of the sub- 

molecular bodies and perhaps by the quasi-dimensional memory. It is 

also interesting to note that so called duplicated remedies show no 

fingerprint under freezing or Kirlian photography. 

Duplicated Remedies and Homoepathic Information Transfer 

As has been discussed, there are several possible modes of information 

transfer. Duplicators work on a supposed magnetic transfer. In the first 

mode, which involves chemical action, magnetics would not work for 

information transfer. In the second and third modes, the mechanical 

force of succussion could change electron or molecular quantic states. 

Magnetics cannot effect this change. If magnetics could indeed do so, 

then homeopathy would be useless. The magnetic interference from a 

T.V. set or a telephone unit would change the information. Transport of a 

homeopathic through the magnetic lines of the earth would change the 

information and nullify homeopathic effectiveness. 

As mentioned, duplicated remedies show no change in freezing 

patterns or in Kirlian photography. Duplicated remedies are probably 

advanced placebo at best. To test this supposition, an experiment was 

performed with double blind capacity. 

Procedure: 35 patients were chosen from a naturopathic Doctor’s 

practice. All patients were using certain homeopathics on a regular basis 

and knew what results to expect. Some patients used a Candida nosode 

to control bloating or other bodily symptoms; others used Belladonna or 

Lachesis. All were familiar with their remedy’s effect. 

Each patient was given either a regular homeopathic or a duplicated 

remedy. Each patient was also given either a placebo sugar pill, or a pill 

with 5mg. Narcan (Naloxone). Naloxone is used to block endorphin 

response and has been found to block the placebo effect in placebo 

responsive patients. Patient profiles were chosen to exclude those with 

24

symptoms of pain as Naloxone can increase pain perception. The test 

was double blind with neither patient nor practitioner knowing which 

formula was given. Patients were given questionnaires to evaluate the 

efficacy of the remedy. Results of the effectiveness are shown in the 

accompanying diagram. 

Results: The tests show that the duplicated remedy performed 

significantly lower than the real remedy. The placebo blocking Narcan 

pill significantly lowered efficacy (63% is approximately the predicted 

placebo effect). 

Perhaps the information transfer of mode number 4 (multi-dimensional 

transfer) could account for the transfer of duplicators; Narcan with its 

endorphin blocking action might also block other dimensional 

information transfer. Even so, the study shows a markedly decreased 

efficacy with the duplicated remedy. Radionic remedies have no 

pharmacology, quantic state or polymorphic state, thus, they are not 

homeopathics and homeopathy is continually blamed for radionic 

remedies that fail. 

Here again, quality is often not paramount to homeopaths. Some prefer 

the greater monetary reward duplicators or imprinters provide. This lack 

of focus on quality and maximization of effectiveness could erode our 

industry. Only through quality and dedication to developing and 

delivering the finest homeopathics can we truly succeed. If you want the 

best, at affordable prices, Dr. Recommend’s remedies are for you. 

DUPLICATION STUDY 

Placebo Duplicated Real 

(Imprinted) Homeopathic 

Placebo 55% 63% 97% 

Narcan 10% 11% 96% 

25

COMPARISON CHART 

NEW HOMEOPATHY ALLOPATHY 

Very small chance of side effects Very great chance of side effects 

Minimal cost Usually high costs 

Safe for children and elderly Warning of risks if not used 

correctly 

Non-addictive Creates dependency 

Works by letting patient reestablish 

homeostasis 

26 

Works by externally blocking, 

stimulating, or interfering with the 

body 

Major malpractice suits. Iatrogenic 

Little if any malpractice, due to 

safety 

disease is on the increase 

Philosophy: body’s reactions are an Philosophy: Body is stupid and 

intelligent attempt to deal with malfunctions often; it then needs to 

toxicity and other disease-causing be stimulated, blocked, or fooled by 

conditions 

the doctor and his synthetic 

medication 

Easy to use Takes years of experience 

Safe for environment, natural Manufacturing hurts environment 

Tries to cure Tries to sedate reactions 

Tries to treat whole body 

Tries to reduce patients to mere 

metabolically 

symptoms 

The patient is an individual The patient is a set of symptoms 

Symptoms are only a part of a Symptoms are bearers of bad news, 

complex set of problems 

and we should kill the messenger 

Pain is God’s gift, and life’s way of Pain is the enemy and must be 

telling us about underlying 

covered up. Improperly reduces 

problems 

inflammation 

Stimulates immune system Weakens immune system. 

Sensitive to energetic problems of Ignores energetic nature of the 

the body 

body

INFLAMMATION 

Part of the Defense Phase of Life 

Sympathetic, Acidosis, Hyaluronidase, Hydrolysis, Tissue Bouillon, 

Hypertony, Histamine 

Homeopathy/Naturopathy Allopathy 

Holistically Driven Symptom Driven 

Defense Management 

Restoration of Homeostasis 

Release of Etiology 

Minimal Dose 

System Balance Restored 

System Release of Auto 

Toxins 

Reduced Cascades 

Proper Anti-Body Release 

Cure 

27 

Suppression 

Chemotherapeutics 

Antibiotics, Antipyretics 

Steroids, Anti-Inflammatories 

NSAID 

Precipitate Develops as 

Biology/Reacts to Synthetic 

Compounds/Mega-Doses of 

Drugs/Builds Dependency 

Produces Wild (Illegal/Improper) 

Peptides (Overdose of Drugs) 

Induces Anti-Body Cascade 

Produces Improper 

Auto Anti-Bodies 

Produces Auto Aggression Diseases: 

Lupus, Arthritis, Asthma, etc.

HOMEOPATHIC INSTRUCTION 

� Take nothing by mouth 10 – 15 minutes prior to and following 

dosage. This includes food, drink, cigarettes, chewing gum, 

toothpaste, etc. 

� Limit caffeine or nicotine in any form, such as soda pop, coffee, 

chocolate, cigarettes. If necessary use one hour after taking a 

homeopathic 

� Limit mint in any form, such as candy mints, mint toothpaste, 

mint mouthwash. 

� No camphor, as in muscle and joint rubs. Avoid moth ball fumes. 

� If dental drilling or trauma to mouth occurs, use topically for 48 

hours. 

� Limit breathing of strong smells, such as paint thinner, 

eucalyptus, cigarette smoke (especially menthol). 

� Limit raw garlic, onions and strong spices to one hour after taking 

a homeopathic. Cooked garlic is ok. 

� Place drops under the tongue and hold for 10 seconds to allow for 

absorption. 

� Keep homeopathics out of direct sunlight and x-ray. 

� Homeopathics may generally be taken at the same time with other 

suggested homeopathics. 

� Homeopathics should not be mixed with Liquitrophics and should 

be taken 20 minutes apart. 

CAUTION: Alcohol sensitivities – If a person is sensitive to alcohol, put 

the drops into a 3 oz. glass of warm water. Allow one minute for alcohol 

to evaporate. Pills are also available without alcohol. By following these 

guidelines, you will give the remedies the greatest opportunity to 

succeed. 

28

THE HORMETIC PHILOSOPHY 

Over the last hundred years, man has drastically increased his toxic 

exposure through the development of synthetics. Present day scientists 

have found in a new study of hormesis that tickle doses, small trace 

doses of a toxin, can have stimulatory effects on the body. Hormesis 

stimulates a cell’s defense system. In hormesis the homeostatic balance 

is tipped, forcing the body to take measures to protect itself or the effect 

where a toxic substance acts like a stimulant in small doses but acts as 

an inhibitor in large doses. 

The Dr. Recommends’ hormetic remedies cover a wide variety of toxic 

conditions including asbestos poisoning, beauty shop toxins, 

environmental toxins, industrial toxins, mercury amalgams and more. 

The Dr. Recommends’ formulas are safe yet powerful in their ability to 

stimulate the individual to detoxify without inducing a healing crisis. The 

high-end potencies used in the Dr. Recommends’ remedies are 

counterbalanced by the lower dose remedies mixed in the homochords. 

These highly engineered hormetic remedies can be used for increased 

safety and effectiveness, producing a more stable and safer remedy for 

doctors to use with their patients. 

29

HORMETIC REMEDIES 

AMEBA-FUGE (1 fl. oz.) 

Catalog No. 0005 

Indication: Ameba infections 

Ingredients: Diloxanide Furoate Metronidazole 3x. Artemisia 

absinthium, Bismuthum Metallicum, Allium sativum, Ipecacuanha 6x. 

Ammonium Phosphoricum 6x, 12x. Ferrum phosphoricum 6x, 12x, 30x. 

Ameba, Entamoeba histolytica, Naegleria fowleri 24x, 40x, 75x, 120x, 

300x, 500x. 

ASBESTOS (1 fl. oz.) 


Indication: Asbestos sensitivity, Assists in detox 

Ingredients: Zincum Valerianicum 5x. Lung sarcode 6x, 12x, 30x, 60x, 

100x. Iodium 12x. Silicea 12x, 30x, 60x. Asbestos 25x, 60x, 100x, 

350x, 500x. 

BACTERIA-FUGE (1 fl. oz.) 


Indication: Bacterial infections 

Ingredients: Hydrastis canadensis 3x, 6x, 12x, 30x, 100x. Zincum 

Metallicum 4x, 12x. Aloe socotrina 6x. Allium sativum, Arum 

maculatum 12x. Mercurius Vivus 16x. Broad-based Bacillinum, 

Pyrogenium, Anthracinum, Staphysagria 16x-30x, 100x. Diphtherinum, 

Streptococcinum, Staphylococcinum, Pneumococcinum, Syphilinum, 

Botulinum, Tuberculinum 16x-30x, 100x, 500-1000x. Eucalyptol 20x. 

Lac caninum, Lac vaccinum 30x. 

COSMETIC MATERIALS (1 fl. oz.) 


Indication: Cosmetic material sensitivity, Assists in detox 

Ingredients: Natrum Carbonicum 4x. Manganum Metallicum 6x. 

Formalinum 10x, 30x, 100x, 500x. Nitricum Acidum, Phosphoricum 

Acidum, Hypophysis, Sulphur 12x. Miscellaneous Beauty Shop Toxins 

30x, 60x, 100x, 750x, 1100x. Kali Cyanatum 20x, 30x, 60x, 100x. 

30

DENTAL MATERIALS (1 fl. oz.) 


Indication: Dental material sensitivity, Assists in detox 

Ingredients: Caries, Gingivitis, Periodontitis 16x, 20x, 30x. Root Ostitis 

20x, 30x. Argentum Metallicum, Mercurius Solubilis, Aurum 

Metallicum, Platinum Metallicum, Dental Materials (Amalgams, 

Composites, Bonding Resins, Dentin Bonders, Cavity Liners, Metals, 

Ceramics, Cements, Temporary Restoratives, Root Canal Materials, 

Anesthetics, Denture Materials, Flourides) 30x, 60x, 100x, 500x, 1000x. 

ENVIRONMENTAL POLLUTANTS (1 fl. oz.) 


Indication: Water and air pollution sensitivity, Assists in detox 

Ingredients: Zincum Metallicum 3x. Chlorophyllum 5x. Manganum 

Metallicum 5x, 12x. Taraxacum officinale 6x, 12x, 30x. Formalinum 8x, 

12x, 30x, 100x, 500x. Petroleum 16x, 20x, 30x, 60x, 100x, 500x, 1000x. 

Air Pollution 50x, 155x, 700x. Water Pollution 50x, 500x. 

Hydrocarbonum 60x. 

FOOD ADDITIVES (1 fl. oz.) 


Indication: Food additive sensitivity, Assists in detox 

Ingredients: Berberis vulgaris, Plantago major 3x, 6x, 12x, 30x. Zincum 

Metallicum, Lycopodium clavatum, Selenium Metallicum 6x, 30x. 

Graphites, Taraxacum officinale, Arctium 8x, 12x. Petroleum 13x, 24x, 

100x, 500x. Miscellaneous Food Additives 30x, 60x, 100x, 500x, 1000x. 

FUNGI-FUGE (1 fl. oz.) 


Indication: Fungal infections 

Ingredients: Tabebuia impetiginosa, Equisetum arvense 3x. Natrum 

Muriaticum 4x. Colostrum 6x, 12x. Bovine Glandulars: Thymus, Liver, 

Lymph, Spleen 5x, 12x, 30x, 60x, 100x. Manganum Metallicum, 

Selenium Metallicum, Zincum Metallicum, Allium sativum 6x. Bovista 

6x, 12x. Usnea barbata, Amanita muscaria, Saccharomyces, Ustilago 

maidis, Borax 6x, 12x, 30x. Apis mellifica 12x. Graphites 16x, 30x. 

Chlorinum, Iodium 20x, 30x, 100x. Candida albicans, Candida 

parapsilosis, Blastomyces, Molds, Epidermophyton, Chlamydia, 

Geotrichum 30x, 60x, 100x, 500x, 1000x, 50m. Mercurius Solubilis, 

Salarinum, Antibiotics 50x, 100x. 

31

HALOGENS (1 fl. oz.) 


Indication: Chlorine or fluorine sensitivity, Assists in detox 

Ingredients: Zincum Metallicum, Selenium Metallicum 6x. Chlorinum, 

Bromium, Fluorine 6x, 12x, 30x, 40x, 100x, 500x, 1000x. Diatomum 

12x, 30x, 60x. Mercury 100x. 

INDUSTRIAL POLLUTANTS (1 fl. oz.) 


Indication: Industrial pollution sensitivity, Assists in detox 

Ingredients: Taraxacum officinale, Chlorophyllum, Plantago major 4x, 

12x, 30x. Selenium Metallicum 6x. Silicea 7x. Plumbum Metallicum 

12x. Zincum Metallicum, Iodium 30x, 60x, 100x. Industrial Toxins 40x, 

40c, 40m. 

INSECTICIDES (1 fl oz.) 


Indication: Insecticide sensitivity, Assists in detoxification. 

Ingredients: Taraxacum officinale, Plantago major 3x. Carduus 

marianus 4x. Natrum Muriaticum 6x. Cholecystokinin, 

Acetylcholinesterase, Acetylcholine 20x, 30x, 60x, 100x. Organo 

Phosphates, Miscellaneous Synthetic Insecticides and Herbicides 30x, 

60x, 100x, 500x, 1000x. 

METALS (1 fl. oz.) 


Indication: Metal sensitivity, Assists in detox 

Ingredients: Plantago major 4x, 6x-12x. Silicea 6x, 12x, 30x. Kali 

Muriaticum, Kali Phosphoricum, Liver Sarcode, Kidney Sarcode: 6x, 

12x, 30x, 60x, 100x. Aluminum Metallicum, Aurum Metallicum, 

Cadmium Metallicum, Beryllium Metallicum, Niccolum Metallicum, 

Mercurius Vivus, Amalgam, Argentum Metallicum, Plumbum Metallicum, 

Stannum Metallicum, Selenium Metallicum, Rubidium, Radon, Radium, 

Cobaltum Metallicum, Molybdenum, Antimony, Uranium, Bismuthum 

Metallicum, Platinum Metallicum 30x-30c, 30m. 

RADIATION (1 fl. oz.) 


Indication: Radiation sensitivity, Assists in detox 

Ingredients: Sodium Alginate 2x. Citrus limonum 3x. Hydrangea 

arborescens 4x. Iodium, Sarcodes: Adrenalinum, Brain, Thyroidinum 

6x, 12x, 30x, 60x, 100x. Imponderables: X-ray, Color TV, Microwave, 

Gamma Radiations 6x, 12x, 30x. Phosphorus 12x. Radium Bromatum 

22x, 60x, 100x, 500x, 1000x. EMR Spectrum 100x. 

32

SYNTHETIC CHEMICALS (1 fl. oz.) 


Indication: Synthetic pharmaceutical sensitivity, Assists in detox 

Ingredients: Natrum Muriaticum 3x. Kali Nitricum 6x. Platinum 

Metallicum 8x. Plumbum Metallicum, Graphites, Lac defloratum 8x, 

12x, 30x, 100x. Vaccinotoxinum 16x, 30x, 60x. Pharmaceutical Toxins 

60x, 100x, 500x, 1000x. 

VERMI-FUGE (1 fl. oz.) 


Indication: Intestinal parasite infections 

Ingredients: Absinthium 3x, 6x. Sulphur 4x. Rhamnus purshiana, 

Cinchona officinalis, Juglans nigra, Ferrum Phosphoricum 6x. 

Magnesium Metallicum 7x. Cymbopogon citratus 8x. Mercurius 

Solubilis 12x. Nosodes of Various Helminths, Nematodes and Intestinal 

Parasites 12x-30x, 60x, 100x, 500x, 1000x. 

VIRAL-FUGE (1 fl. oz.) 


Indication: Viral infections 

Ingredients: Trifolium pratense, Echinacea purpurea, Natrum 

Muriaticum, Asclepias tuberosa, Ferrum Iodatum, Zincum Metallicum 

3x. Ferrum Phosphoricum 4x. Lac Vaccinum, Euphrasia officinalis 6x. 

Thuja occidentalis 6x, 12x, 30x, 60x, 100x. Camphora, Calcarea 

Arsenicica, Arium Virus, Ichthyolum, Selenium Metallicum 12x. 

Vaccinotoxinum, Morinum, Variolinum, Miscellaneous Influenzinum, 

Psorinum, Vincetoxicum 12x, 30x, 60x, 100x, 500x, 1000x, 50m. Aurum 

Metallicum, Platinum Metallicum, Uranium 60x-100x. 

33

NOSODES 

Nosodal therapy involves using disease-causing or disease-containing 

tissues and diluting them to cause reversal effects. This is the basic 

principle of vaccination and homeopathy. Diseased tissue can be used to 

alleviate disease conditions. This is the science of nosodal homeopathy. A 

nosode is a homeopathic or diluted and energized form of the diseased 

entity. 

Within this treatise, a list of the following are included: bacteria, 

worms, viruses, fungi, protozoa, rickettsia, and many other tissues; as 

well as medical nosodes of various diseases and diseased tissues. Also 

included are: dental toxins that allow the dentist to use different disease- 

causing dental material from the nosodal tray. 

There is a wide range of nosodal factors used by modern homeopaths. 

Those known to Dr. Nelson are contained in this document. To reference 

some experimental data behind nosodal homeopathy we point the reader 

to The Experimental Data on Homeopathy, by Dr. William Nelson. Within 

the pages of that document one can read about how nosodal homeopathy 

is used to reverse disease conditions. 

Homeopathy offers a safe alternative to vaccination which has very 

similar modes of operation. Even new ideas of DNA and RNA theory can 

be ascertained with this new homeopathy. 

34

VIRUSES 

CONJUNTIVITIS, VIRAL 

COMMON WARTS AND 

CONDOMYLOMA 

COXSACKIE 

DIPTHERIA 

EPSTEIN BARR 

ESCHERICOLI VIRAL 

COMPONENT 

FAEKALALK 

HEPATITIS A 

HEPATITIS B 

HERPES PROGENTALIS 

HERPES SIMPLEX 

HERPES ZOSTER 

HUMAN PAPPILOMA VIRUS 

INFECTIOUS MONONUCLEOSIS 

INFLUENCINIUM 

INFLUENZA 

INFLUENZA (BERIN 55) 

INFLUENZA 83 

INFLUENZA 84 

INFLUENZA 85 

INFLUENZA 86 

INFLUENZA 87 

INFLUENZA 88 

35 

MALARIA 

MONILA ALBACANS VIRAL 

COMPONENT 

NOSLAMINT 

PLANTERS WARTS 

POLIO MYELITIS 

Q FEVER 

RETRO-VIR 

RHINOPNEUMONIA 

ROCKY MOUNTAIN SPOTTED 

FEVER 

SWINE INFLUENZA 

TRICHINOSIS 

V GRIPPE 

VAPCH GRIPPE 

VA2 GRIPPE 

VA2 LGRIPPE 

V2 GRIPPE 

V3 GRIPPE 

V4 GRIPPE 

V5 GRIPPE 

V20 GRIPPE–V50 GRIPPE 

V60 GRIPPE–V76 GRIPPE 

RETROVIRUS1–RETROVIRUS10 

VIRUS

FUNGUS 

ADNEXITIS 

ASPERGILLUS, FLAVUS, 

FUMIGATUS, GLAUCUS, 

NIGER, TERRUS 

BLASTOMYCOCES 1 




CANDIDA ALBICANS 

CANDIDA GLABRATA 

CANDIDA GUILLIER 

CANDIDA KRUSEI 

CANDIDA LAUERENTI 

CANDIDA LIPOLYTI 

CANDIDA LUSITANI 

CANDIDA ORIENTALIS 

CANDIDA PARAPSILOSA 

CANDIDA PSEUDOTROPICALIS 

CANDIDA RUGOSA 

CANDIDA STELLATO 

CANDIDA TAMATA 

CANDIDA TROPICALIS 

CRYPTOTOCCUS 1 



36 



CYRTOCOCUS NEOFORMS 

EPIDERMOPHYTON 1 




FUNGUS FLORA 

HISTOPLASMOSIS 1 



HISTOPLAMSOSIS 4 


NEOFORMS 1 

NEOFORMS 2 

NEOFORMS 3 

PNEUMOCYSTOSIS 

SACROMYCOSES 1 – 

SACROMYCOSES 7 

SCEREVISI 

TINEA CURTIS 

TINEA CURVIS 

TINEA PEDIS 

TYCO SPORON

BACTERIA 

ACTINOMYSOSIS 

ADNEXITIS 

AEROBACTER 

AMOEBA 

AMOEBA HEPAR ABSCESSUS 

ANTHRAX 

ASCARIDINUM 

BAC. GARTNER 

BAC. MORGAN 

BACILLUS ANTHRACIS – ANTHRAX, MALIGNANT PUSTULE 

BACTEROIDES 

BARTONELLOSIS 

BIFIDUS 

BOTULINUM 

BRUCELLOSIS 

CARIES 

CAUCAUOUS 

CHLAMYDIA TRACHOMATIS 

CHOLERA 

DYSENTERY 

ECOLI 

ENCEPHALITIS 

ENTEROCOCCINUM 

FRANCISELLA TULARENIS – TULAREMIA 

GASTROENTEROCOLI 

HAEMOPHILUS INFLUENZA 

KAWASAKI 

KLEBSIELLA PNEUMONIAE 

LEGIONELLA 

LISTERIA MONOCYTOGENES 

LYMES 

MELIOIDOSIS 

MENINGOCOCCINUM 

MORBILLINUM 

MYCOPLASMA PNEUMONIAE 

MYOBACTERIUM LEPRAE – LEPROMATOUS LEPROSY 

NEISSERIA GONORRHOEAE 

NOCARDIA 

NOS. ELEPHANTIASIS 

NOS. FISHPYROGENIUM (FRESHWATER) 

NOS. RHINOPNEUMONITIS 

OXYUREN 

PEPTOSTREPTOCOCCUS ANAER. 

PLASMODIUM SPP. – MALARIA 

37

BACTERIA, cont. 

PNEUMOCCIN 

PNEUMOCOCCUS 

PROGENIUM 

PROPIONIBACTERIUM ACNES – ACNE 

PROTEUS 

PSEUDOMONAS 

PYOCYANEUS 

R. MOOSERI 

R. QUINTANA – TRENCH FEVER 

R. RICKETTESII 

RICKETTSIA PROWAZEKII 

RUBEOLA 

SAB ACIDOPHILUS/BIFIDUS 

SALMONELLA TP 

SCARLATINUM 

SHIGA KRUSE 

SHIGELLA PARADYSENTERIAE 

SPRILLUL MINUS – RAT-BITE FEVER 

STAPHYL AUREUS 

STAPHYL PYOGENES – IMPETIGO 

STAPHYLOCOCCIN 

STAPHYLOCOCCUS EPIDERMIDIS – ACNE 

STREPTOBACILLUS MONILIFORMIS – RAT-BITE FEVER 

STREPTOCOCCIN 

STREPTOCOCCUS HAEMOLYTICUS 

SYPHILIS 

TERSENIA PESTIS – PLAGUE 

TETANUS 

THERMAL BACTERIA 

TOXOPLASMOSIS 

TREPONEMA CARATEUM – PINTA 

TREPONEMA PALLIDUM – SYPHILIS (SECONDARY) 

TREPONEMA PERTENUE – YAWS 

TRICHINELLA SPIRALIS, MAN 

TUBERCULINUM 

TULEREMIA 

TYPHOIDINUM 

TYPHUS 

VACCININUM 

38

NOSODES, DENTAL 

ASTRO 1180 

AUTOPOLYMERISAT 

(AUTOACRYLAT) 

BARRIER 

BIO C 

BIO H 

C & B METABOND 

CARBOCAINE 2% 

CARBOCAINE 3% 

CARBOXYLAT-CEMENT 

CAVIT-G 

CERAMCO II 

COMPOS FULL MATERIAL 

COMPSPAN OPAQUE 

COMPSPAN RESIN 

CONCEPT 

CONQUEST DF 

COPALITE 

COPPERAMALGAM 

DEGUNDENT G 

DENTAL GOLD 

DG-63 

DICOR 

DISPERSAL 

CURELON 

DYCAL 

E-2713 

EBA 

FIRMILAY 

FLECK’S 

GC DENTIN CEMENT 

GEL KAM 

GINGIVITIS 

GLUMA PART 3 

GUTTA PERCHA 

HELIOBOND 

HELIOMOLAR 

HERCULITE XR 

HYDROXYAPATITE 

HYDROXYLINE 

HP-3 

IN-CERAM 

JELENKO O 

JET ACRYLIC 

39 

KETAC-CEM 

LIFE 

LUCITONE 199 

MARCAINE 

MOLYBDENUM 

NOBILIUM 

NOS. ACUTE BACTERIAL 

OSTITIS OF THE JAW 

NOS. ACUTE PULPITIS 

NOS. APICAL GRANULOMA 

NOS. CARIES 

NOS. CHRON. BACT. OSTITIS 

OF JAW 

NOS. CHRON. PULPITIS 

NOS. CORYNEBACTERIUM 

NOS. CYST EPITHELIAL 

NOS. DENTAL SACK 

NOS. EAR SCLEROSIS 

NOS. EPULIS 

NOS. EXUDATIVE OSTITIS 

NOS. FATTY OSTITIS OF JAW 

NOS. FISTULA DENTALIS 

NOS. FOLLICLUARE CYST 

NOS. FUNDUS ABSCESS 

NOS. GANGRANOSE PULPA 

NOS. GINGIVITIS 

NOS. GRANULMOA PURULENT 

NOS. JAW OSTITIS 

NOS. NECROTIC GINGIVITIS 

NOS. OSTEOSCLEROSIS 

OF THE JAW 

NOS. PARODONTOSE 

NOS. PAROTIS DENTAL 

CALCULI 

NOS. PARULIS (STAPH. AUX.) 

NOS. PARULIS (STREPTOC. 

MUC.) 

NOS. PERIODONTAL FIBROM 

NOS. PERIODONTAL POCKET 

NOS. PERIODONTITIS 

NOS. PULPAL STONE 

NOS. RADICULAR CYST 

NOS. ROOT CANAL TX 

NOS. ROOT GRANULOMIUM

NOSODES, DENTAL, cont. 

NOS. ULCERATIVE GINGIVITIS 

NUPRO NEUTRAL 

OCCLUSIN 

OLYMPIA 

OPTEC DENTIN 

OPTEC HSP 

OPTEC U-BOND 

ORAL MUCOCUTANEUS 

PAPILOMA 

P-10 

P-50 

PALLADIUM SILVER 

PERTAC 

PHOSPHATE-CEMENT 

POLYMERISAT (ACRYLAT) 

PORSELITE DUAL 

POST-COM II 

PRISMA APH 

PRISMA DENTIN 

PRISMA U-BOND 3 

PROFILE 

PROTEMP 

PULP CANAL SEALER 

PULPDENT 

40 

PURE ALLOY 

REXILLIUM V 

ROOT GRANULOMIUM 

RX-IV 

SCOTCHBOND II 

SCOTCHPREP 

SEALAPEX 

SILUX PLUS 

SODIUM FLUORIDE 

SPC PERIODONTO COMPLEX 

STAINLESS STEEL 

TERM 

TICONIUM 

TITANIUM 

TITANIUM ALLOY 

TRIADVLC 

VINYLPOLYMERISAT 

VITA VMK 68 

VITADUR N 

VITRA BOND 

2-1 

XR BAND 

XR DENTIN 

XYLOCAINE 2% 

ZOE 2200 

ZONE

NOSODES, MEDICAL 

ACID PHOSPHATES 

ALBUMIN, COWMILK 

ALKALINE PHOSPHATASE 

ALPHA GLOBULIN 

ALPHA1 GLOBULIN 

ALPHA2 GLOBULIN 

ALUMINUM SERUM 

ALUMINUM WHOLE BLOOD 

AMPYCILLIN 

ARTERIAL OXYGEN AFTER 

PURE OXYGEN 

ARTERIAL OXYGEN 

SATURATION 

ASTHMA BRONCHITIS 

BASOS 

BETA GLOBULIN 

BICARBONATE SERUM 

BLEEDING TIME 

BLOOD AMMONIA 

BLOOD LACTATE LEVEL 

BLOOD PYRUVATE LEVEL 

BLOOD UREA NITRATE 

LEVEL 

BLOOD VOLUME 

BUN 

CADMIUM SERUM 

CADMIUM WHOLE BLOOD 

CALCIUM SERUM 

CALCIUM WHOLE BLOOD 

CALCULI PROSTATAE 

CALCULI RENALES 

CALCULI RENALES 

OXALIC ACID 

CALCULI VESICALES 

CAPILLARY FRAGILITY 

CATARACTA BRUNESCENS 

CATARACTA COMPLICAT 

CELL MORPHOLOGY 

CHOLESTEROL 

CHOLESTEROL ESTER 

SERUM 

CHROMIUM SERUM 

CHRONIC CYSTITIS AND 

ENDOMETRIOSIS 

41 

CONTARACTA SENILIS 

CO2 CONTENT 

COPPER SERUM 

CPK 

CR. WHOLE BLOOD 

CU. WHOLE BLOOD 

CREATINE 

CREATINI 

DIFFERENTIAL TESTS 

ENCEPHALOMELOMALACIA 

ENDOMETRITIS 

TUBERCULOSSA 

EOSINOPHIL 

FASTING BLOOD SUGAR 

GALACTOSE IN BLOOD 

GAMMA GLOBULIN 

GLOBULIN 

GLUCOSE 

HEMOGLOBIN 

HEPATITIS 

IRON SERUM 

IRON WHOLE BLOOD 

LACTIC DEHYDROGENASE 

LDH 

LEAD SERUM 

LEAD WHOLE BLOOD 

LIPID TRIGLYCER 

LIPOPROTEIN SERUM 

LUPUS 

LUPUS ERYTHEMATOSIS 

LYMPHS 

MANGANESE 

MERCURY SERUM 

MERCURY WHOLE BLOOD 

MN. WHOLE BLOOD 

MONOS 

MULTIPLE SCLEROSIS 

NERUALGIE 

NEUROFIBROM 

NICKEL SERUM 

NICKEL WHOLE BLOOD 

NODULAR PROSTATIC 

HYPERPLASIA 

NOS. BLADDER BIHARZIOSIS

NOSODES, MEDICAL, cont. 

NOS. BLADDER POLYP 

NOS. BLADDER Tbc 

NOS. CYSTOPYELITIS 

NOS. FIBROADENOM 

MAMMA 

NOS. KIDNEY PAPILOMA 

NOS. MAMMA FIBROMATOSIS 

NOS. MASTITIS 

NOS. MASTOPATHIA CYSTICA 

NOS. OXALIC ACID URICA 

NOS. PERIORCHITIS 

NOS. PROSTATA-ADENOM 

NOS. SOLITARY CYST (KIDNEY) 

NOS. TESTICULAR FISTULA Tbc 

NOS URETHRITIS POST MASC 

PARTIAL THROMBOPLASTIN 

TIME 

PHOSPHATE SERUM 

PHOSPHATE WHOLE BLOOD 

PHOSPHOLIPIDS 

PLASMA KETONES 

PLATELET COUNT 

PLEURITIS 

POTASSIUM SERUM 

POTASSIUM WHOLE BLOOD 

PROGRESSIVE MUSCULAR 

DYSTROPHIE 

PROTHROMBIN CONSUMPTION 

PROTHROMBIN TIME 

PSA 

PSORIASIS 

RED BLOOD COUNT 

RESIDUAL VOLUME 

RETICULOCYTE 

SE. WHOLE BLOOD 

SEGS PMN 

SELENIUM SERUM 

SGOT 

SGPT 

SINUSITIS FLONTALIS 

SINUSITIS MAXILLARIS 

42 

SODIUM SERUM 

SODIUM WHOLE BLOOD 

SPIROMETRIC STUDIES 

THROMBIN TIME 

TIMED VITAL CAPACITY 

TONSILLA 

TONSILLA PHARYNGEA 

TOTAL BILIRUBIN 

TOTAL LIPIDS 

TOTAL LUNG CAPACITY 

TOTAL PROTEIN 

TRANSAMINASES 

TRICHOMONAS VAGINITIS 

T3 VERTEBRAE 

T4 VERTEBRAE 

T7 VERTEBRAE 

URIC ACID 

VAGINITIS 

VITAL CAPACITY 

WBC 

WILSON 

ZINC SERUM 

ZINC WHOLE BLOOD 

2 HOUR POSTPRANDIAL 

BLOOD SERUM

PARASITES 

AMIDOSTOMUM ANSERIS, BIRD 

ANCYLOSTOMA CANIUM, DOG, CAT 

ANCYLOSTOMA DUODENALE, MAN 

ANCYLOSTOMA TUBAEFORME, CAT 

ANGIOSTRONGYLUS CANTONENSIS, MAN 

ANGIOSTRONGYLUS VASORUM, DOG 

ANOPLOCEPHALA MAGNA, HORSE 

APOPHALLUS DONICUS, DOG, CAT 

ASCARIDIA GALLI, BIRD 

ASCARIS LUMBRICOIDES, MAN 

ASCAROPS STRONGYLINA, PIG 

ASPICULIRIS TETRAPTERA, MOUSE, RAT 

CAPILLARIA AEROPHILA, CAT, DOG 

CAPILLARIA BREVIPES, BIRD 

CAPILLARIA FELIS-CATI, CAT 

CAPILLARIA OBSIGNATA, BIRD 

CAPILLARIA PLICA, DOG 

CAPILLARIA PUTORII, DOG, CAT 

CATATROPIS VERRUCOSA, BIRD 

CHILOMASTIX MESNILI, MAN 

CYATHOSTOMA SPP., HORSE 

CYSTICAULUS OCREATUS, SHEEP 

DAVAINEA PROGLOTTINA, BIRD 

DELAFONDIA VULGARIS, HORSE 

DICROCOELIUM LANCEATUM, MAN 

DICTYOCAULUS FILARIA, SHEEP 

DIENTAMOEBA FRAGILIS, MAN 

DIOCTOPHYMA RENALE, DOG 

DIPHYLLOBOTHRIUM LATUM, MAN, DOG, CAT 

DIPYLIDIUM CANINUM, MAN, DOG, CAT 

DIROFILARIA IMMITIS, DOG 

ECHINOCOCCUS GRANULOSUS, DOG 

ECHINOCOCCUS MULTILOCULARIS, DOG 

ECHINOSTOMA RECURVATUM, BIRD 

ECHINOSTOMA REVOLUTUM, BIRD 

ENDOLIMAX NANA, MAN 

ENTAMOEBA COLI, MAN 

ENTAMOEBA GINGIVALIS, MAN 

ENTAMOEBA HISTOLYTICA, MAN 

ENTEROBIUS VERMICULARIS, MAN 

FASCIOLA HEPATICA, MAN 

GIARDIA LAMBLIA 

GRAPHIDIUM STRIGOSUM, HARE 

43

PARASITES, cont. 

HABRONEMA MUSCAE, HORSE 

HAEMONCUS CONTORTUS, SHEEP 

HAEMONCUS PLACEI, CATTLE 

HETERAKIS GALLINARUM, BIRD 

HYDATIGERA TAENIAEFORMIS, DOG, CAT 

HYMENOLEPIS DIMINUTA, MAN 

HYMENOLEPIS NANA, MAN 

IODAMOEBA WILLIAMS, MAN 

MARSHALLAGIA MARSHALLI, MAN 

MESOCESTOIDES LINEATUS, DOG, CAT 

MESOSTEPHANUS SP., CAT 

METASTRONGYLINAE, PIG 

MEULTBRAU 

MUELLERIUS CAPILLARIS, SHEEP 

MULTICEPS GAIGERI, DOG 

MULTICEPS MULTICEPS, DOG 

MULTICEPS SERIALIS, DOG 

MULTICEPS SMYTHI, DOG 

NECATOR AMERICANUS, MAN 

NEMATODIRUS FILICOLLIS, CATTLE 

NEMATODIRUS SPATHIGER, CATTLE 

NEMATOSPIROIDES DUBIA, RAT, MOUSE 

NIPPOSTRONGYLUS BRASILIENSIS, RAT, MOUSE 

OESOPHAGOSTOMUM DENTATUM, PIC 

OLLULANUS TRICUSPIS, DOG, CAT 

ONCHOCERCA, MAN 

OPISTORCHIS FELINEUS, MAN 

PARAMPHIS CERVI, CATTLE 

PROBSTMAYRIA VIVIPARA, HORSE 

PROSTHOGONUMUS OVATUS, BIRD 

PROTOSTRONGYLUS RUFESCENS, SHEEP 

RAILLIETINA ECHINOBOTHRIDA, BIRD 

SCHISTOSOMA BOVIS, CATTLE 

SCHISTOSOMA HAEMATOBIUM, MAN 

SCHISTOSOMA MANSONI, MAN 

SPIROCERCA LUPI, DOG 

STEPHANURUS DENTATUS, PIG 

STRONGYLOIDES STERCORALIS, MAN, DOG, CAT 

STRONGYLUS EQUINUS, HORSE 

SYNGAMUS TRACHEA, BIRDS 

SYPHACIA MURIS, RAT, MOUSE 

SYPHACIA OBVELATA, MOUSE, RAT 

TAENIA CERVI, DOG 

TAENIA CRASSICEPS, DOG 

44

PARASITES, cont. 

TAENIA HYDATIGENA, DOG, CAT 

TAENIA KRABBEI, DOG 

TAENIA OVIS, DOG 

TAENIA PISIFORMIS, DOG, CAT 

TAENIA SAGINATUM, MAN 

TAENIA SOLIUM, MAN 

THELAZIA RHODESII, CATTLE 

TOXASCARIS LEONINA, DOG 

TOXOCARA CANIS, DOG 

TOXOCARA CATI, CAT 

TRICHINELLA SPIRALIS, MAN 

TRICHOMONAS HOMINIS, MAN 

TRICHOSTRONGYLUS AXEI, CATTLE 

TRICHOSTRONGYLUS TENUIS, BIRDS 

TRICHURIS SERRATA, CAT 

TRICHURIS TRICHIURA, MAN 

TRICHURIS VULPIS, DOG 

TROPISURUS FISSIINUS, BIRD 

UNCINARIA STENOCEPHALA, DOG, CAT 

45

ISODES 

It is stated in The Experimental Data on Homeopathy by Dr. William 

Nelson, that isodal homeopathy includes using different synthetic 

compounds that can cause disease, even including body secretions. The 

form of isodal therapy that we will concentrate on is that of different 

synthetic compounds and pollutants that can cause disease. Dr. Nelson 

has devised many combinations known as xenobiotics that deal with 

broad-based detoxification. There is also a large list of pollutants that 

can be developed in homeopathic form and various combinations for 

trained homeopaths to use. 

In this chapter there is a long list of pollutants and disease-causing 

factors caused from heavy metals, insecticides, food additives, etc., 

included. This challenging form of homeopathy offers exciting new ways 

to deal with an increasingly polluted world. Many of these compounds 

have the potential to be extremely dangerous and must have strict 

controls which are exercised by Dr. Recommends. It is necessary to make 

sure that the items rendered by licensed doctors are safe to use. The 

pledge of Dr. Recommends is to make safety very important. 

Welcome reader to an exciting new world of expanded homeopathy, a 

world that was unknown to Hahnemann as many of these chemicals did 

not exist during his time, but they are a big part of the structure of 

disease today. Our patients must be cleansed and detoxified of these 

noxious chemicals. In The Experimental Data on Homeopathy, evidence is 

offered for homeopathy’s effectiveness in this area. The new field of 

hormesis research also offers additional evidence for isodal homeopathy’s 

ability to help the patient. 

46

POLLUTANTS I 

ABIETIC ACID 

ABRIN 

ACENAPHTHENE 

ACERDOL 

ACETAL 

ACETAMIDE 

ACETAMIDINE 

HYDROCHLORIDE 

ACETATE RAYON 

ACETOACET-o-CHLORANILIDE 

ACETOACETIC ACID 

ACETOGUANAMINE 

ACETONE PEROXIDE 

ACETONE SEMICARBAZONE 

ACETULAN 

ACETYL IODIDE 

ACETYL TRIETHYL CITRATE 

ACETYBUTYROLACTONE 

ACETYLENE 

ACETYLENE TETRACHLORIDE 

ACETYLSALICYLIC ACID 

ACRIDINE 

ACROLEIN 

ACTINIUM 

ADIPIC ACID 

ADIPONITRILE 

ALDRIN 

ALIZARIN 

ALKALOID SALTS 

ALLOXANTIN 

ALLYL AMINE 

ALLYL CHLORIDE 

ALLYL CHLOROPHENYL 

CARBONATE 

ALLYL FLUORIDE 

ALLYL FORMATE 

ALLYL IODIDE 

ALLYL THIOUREA 

ALLYLENE 

ALUMINUM BROMIDE 

ALUMINUM BROMATE 

ALUMINUM CARBIDE 

ALUMINUM CHLORATE 

ALUMINUM CHLORIDE 

47 

ALUMINUM FLUORIDE 

ALUMINUM FORMATE 

ALUMINUM METHYL 

ALUMINUM PICRATE 

ALVARTHR 

ALYPIN 

AMATOL 

AMINOMETHANE 

AMINOPTERIN 

AMINOPYRINE 

AMMONIA-d3 

AMMONIA GAS 

AMMONIUM ARSENATE 

AMMONIUM AZIDE 

AMMONIUM BICHROMATE 

AMMONIUM BIFLUORIDE 

AMMONIUM BINOXALATE 

AMMONIUM BROMATE 

AMMONIUM CHLORATE 

AMMONIUM CHLOROOSMATE 

AMMONIUM 

CHLOROPALLADITE 

AMMONIUM CYANIDE 

AMMONIUM EMBELATE 

AMMONIUM FLUOGALLATE 

AMMONIUM PICRATE 

AMMONIUM SELENITE 

AMMONIUM THIOCYANATE 

AMYL ALCOHOL 

AMYL NITRITE 

AMYL SILICATE 

AMYLOFORM 

ANABASINE 

ANILINE 

ANILINE BRILLIANT GREEN 

ANILINE FLUORIDE 

ANILINE GREEN 

ANILINE HYDROCHLORIDE 

ANILITE 

ANISOLE 

ANTHRAROBIN 

ANTIMONY TRIETHYL 

ANTIPYRINE 

APHRODINE, YOHIMBINE

POLLUTANTS I, cont. 

APOMORPHINE 

ARSANILIC ACID 

ARSENIC 

ARSENIC TRISELENIDE 

ARSENIC TRISULFIDE 

ARSENOBENZENE 

ARSINE 

ASCARIDOLE 

ASPIRIN 

ATROPINE 

AUROUS CYANIDE 

AUTUNITE 

AZOBENZENE 

AZOCHLORAMIDE 

n-AMYLENE 

o-AMINOETHYLBENZENE 

p-AMINOBENZOIC ACID 

sec-AMYL ACETATE 

sec-n-AMYL ALCOHOL 

2-ACETAMIDOFLUORENE 

2-AMINOETHANOL 

BARBITUATES 

BARIUM ARSENIDE 

BARIUM CARBIDE 

BARIUM CHLORIDE 

BARIUM CHROMATE 

BARIUM CYANIDE 

BARIUM MYRISTATE 

BARIUM NITRATE 

48 

BEETHLE 

BENZALDEHYDE 

BENZEDRINE 

BENZENE 

BENZENE HEXACHLORIDE 

BENZHYDROL 

BENZIDINE 

BENZIL 

BENZOIC ACID 

BENZOIN 

BENZYL MRCAPTAN 

BENZYLAMINE 

BERYL 

BERBERINE 

BETA RAYS 

BETEL 

BIMETHYL 

BISMUTH 

BISULFITES 

BITHIONOL 

BORAX 

BORAZOLE 

BORIC ACID 

BOROCAINE 

BROMATES 

BROMIDES 

BUTYLATED HYDROXYANISOLE 

n-BUTYL GLYCIDYL ETHER 

DI-TERT-BUTYL –p-CRESOL 

HIGH EXPLOSIVES

POLLUTANTS II 

BROMINE 

BROMOPHORM 

BROMOPICRIN 

BRUCINE 

BUTANE 

BUTANOL ALCOHOL 

BUTYL ALCOHOL 

BUTESIN 

BUTOXYL 

BUTYLAMINE 

BUTYN 

BUTYRIC ACID 

BUTYRONE 

2-BUTYNE 

CACODYL 

CADMIUM SERUM 

CAFFEINE 

CALCIMINE 

CALCITE 

CALCIUM CYANAMIDE 

CALCIUM HYDROXIDE 

CAMPHENE 

CAMPHOR 

CANNABIS 

CANTHARIDES 

CAPROIC ACID 

CAPRYLIC ACID 

CARBAMIDE 

CARBITOL 

CARBOLIC ACID 

CARBOLINEUM 

CARBON TETRACHLORIDE 

CARBONYLS 

CARBORUNDUM 

CARBOWAX 

CARNAUBA WAX 

CELLOIDIN 

CELLULOID 

CERIUM 

CESIUM 

CETAB 

CEVADINE 

CHELIDONINE 

CHLORAL 

49 

CHLORAL HYDRATE 

CHLORATES 

CHLORAZINE 

CHLORDANE 

CHLOREX 

CHLORIC ACID 

CHLORINATED NAPHTHALENES 

CHLORINE DIOXIDE 

CHLORINE HYDRATE 

CHLORINE TRIFLUORIDE 

CHLOROACETONE 

CHLOROALDEHYDE 

CHLORHYDO 

CHLORIDES 

CHLORINE 

CHLOROBENZENE 

CHLOROBENZOL 

CHLOROBUTANOL 

CHLOROETHENE 

CHLOROETHYNE 

CHLOROFORMIUM 

CHLOROPICRIN 

CHLOROPRENE 

CYCLOHEXANE 

m-CHLOROANILINE 

m-CHLORONITROBENZENE 

m-CHLOROPHENOL 

o-CHLOROPHENOL 

m-CHLOROPHENYL 

ISOCYANATE 

o-CHLOROPHENYL ISOCYANATE 

p-CHLORO-o-NITROANILINE 

2-CHLORO-6-NITROTOLUENE 

DECALIN 

DEMETON 

DIBORANE 

DICOBALT OCTACARBONYL 

DIETHYL CARBONATE 

DIETHYL SULFATE 

DIETHYLAMINE 

DIETHYLENE GLYCOL 

DIETHYLPHOSPHINE 

DIHYDROPYRAN 

DIIODOACETYLENE

POLLUTANTS II, cont. 

DIIODOFORMOXIME 

DIKETENE 

DIMETHYL BERYLLIUM 

DIMETHYL ETHER 

DIMETHYL SULFATE 

DIMETHYLDIOXANE 

DINITRO-o-sec-BUTYL PHENOL 

DINITROCHLOROHYDRIN 

DINITRODICHLOROBENZENE 

DINITROGEN TRIOXIDE 

DIONIN 

DIPHENYL 

DIPHENYLCYANOARSINE 

DIPHOSGENE 

DITAINE 

o-DIMETHYL PHTHALATE 

ECGONINE 

EMERY 

EPHEDRINE HCL 

ETHYL ACETATE 

ETHYL ACRYLATE 

ETHYL ALCOHOL 

ETHYL BROMIDE 

ETHYL BUTYL KETONE 

ETHYL ETHER 

ETHYL FLUOROSULFONATE 

ETHYL IODIDE 

ETHYL ISOTHIOCYANATE 

ETHYL MERCAPTAN 

ETHYL NITRATE 

50 

ETHYL OXALATE 

ETHYL SILICATE 

ETHYL TRICHLOROSILANE 

ETHYLAMINE 

ETHYLBENZENE 

ETHYLDICHLOROARSINE 

ETHYLENE CHLOROBROMIDE 

ETHYLENE GLYCOL 

ETHYLENEDIAMINE 

ETHYLIDENE CHLORIDE 

FERBAM 

FERRIC NITRATE 

FERRIC OXALATE 

FERRIC SULFIDE 

FIBERGLASS 

FLUOACETATES 

FLUOBERYLLATES 

FLUORIDES 

FLUOROACETIC ACIDE 

FLUOSILICATES 

FLUOSULFONIC ACID 

FORMALDEHYDE 

DEHYDROGENASE 

FORMIC ACID 

FORMYL FLUORIDE 

FURAN 

FURFURAL 

GAMBOGE 

GASOLINE

POLLUTANTS III 

GILSONITE 

SLYCERYL DIACETATE 

GLYOXAL 

GRANITE DUST 

HANANE 

HENNA 

HEPTAFLUOROUTYRIC ACID 

HEPTANE 

HEPTYL ACETATE 

HEXACHLOROACETONE 

HEXACHLOROMETHYL ETHER 

HEXACHLORONAPHTHALENE 

HEXACHLOROPROPENE 

HEXAETHYL TETRAPHOSPHATE 

HEXENE-1 

HYDRAZINE 

HYDRAZOIC ACID 

HYDROCHLORIC ACID 

HYDROFLUORIC ACID 

HYDROFLUOSILICIC ACID 

HYDROGEN PEROXIDE 

HYDROGEN SELENIDE 

HYDROXYLAMINE 

HYPOIODOUS ACID 

p-HYDROQUINONE 

INDIUM 

IODIC ACID 

IODOFORM 

IPECAC 

IROKO 

IRON PENTACARBONYL 

ISOAMYL ACETATE 

ISOAMYL FORMATE 

ISOBUTYL ALCOHOL 

ISOOCTANE 

ISOPRENE 

ISOPROPYL ALCOHOL 

ISOPROPYL ETHER 

ISOPROPYLAMINE 

JUNIPER BERRIES 

KAPOK 

KEROSENE 

KETENE 

KRYOFIN 

51 

LACQUERS 

LACTIC ACID 

LANTHANUM SULFATE 

LAUDANINE 

LEAD AZIDE 

LITHIUM ORATATE (PILL) 

LUMINAL 

LUPERCO 

LUPERSOL 

LUPININE 

LYCONINE 

NICKEL ARSENIDE 

NICKEL CARBIDE 

NICKEL CARBONYL 

NICKEL CHLORATE 

NICKEL CHLORIDE 

NICKEL IODIDE 

NICKEL NITRATE 

NICKEL PEROXIDE 

NICKEL SULFATE 

NICOTINE 

NICOTINE SULFATE 

NIRVANOL 

NITRIC ACID 

NITRIC OXIDE 

NITRITES 

NITROBENZENE 

NITROETHANE 

NITROGEN CHLORIDE 

NITROGLYCERIN 

NITRONAPHTHALENE 

NITROPRUSSIDES 

NITROSYL BROMIDE 

NITROSYL SULFURIC ACID 

NITRYL CHLORIDE 

NORNICOTINE 

p-NITROPHENOL 

OCTACHLORO-CAMPHENE 

OCTADECYL 

TRICHLOROSILANE 

OCTAMETHYL 

PYROPHOSPHORAMIDE 

OCTANE 

OCTYL ALDEHYDE

POLLUTANTS III, cont. 

OLEFINS 

OLEUM 

OPIUM 

ORRIS 

ORTOL 

OXALATES 

OXALIC ACID 

OXALYL CHLORIDE 

52

POLLUTANTS IV 

OZONE 

PARAFORMALDEHYDE 

PARALDEHYDE 

PARATHION 

PELARGONIC MORPHOLIDE 

PENTACHLOROMETHYL ETHER 

PENTACHLORONAPHTHALENE 

PENTACHLOROPHENOL 

PENTASOL 

PERBENZOIOC ACID 

PERCHLORATES 

PERCHLORIC ACID 

PERCHLOROETHYLENE 

PERIODIC ACID 

PERONINE 

PEROXY SULFURIC ACID 

PERTHANE 

PHENACAINE HYDROCHLORIDE 

PHENOTHIAZINE 

PHENOTHIOXIN 

PHENYL CARBYLAMINE 

CHLORIDE 

PHENYL MUSTARD OIL 

PHENYLHYDRAZINE 

PHENYLTRICHLOROSILANE 

PHOSGENE 

PHOSPHINE 

PHYSOSTIGMA 

PICRIC ACID 

POTASSIUM IODIDE 

POTASSIUM NITRITE 

POTASSIUM PERSULFATE 

PROCAINE HYDROCHLORIDE 

PROPIOLACTONE 

PROPIONYL CHLORIDE 

PROPYL ALDEHYDE 

PROPYLENE 

PROPYLENE ETHER 

PROPYLENE OXIDE 

PROTACTINIUM 

PTOMAINES 

PYRETHRUM FLOWERS 

PYRIDINE 

PYROGALLOL 

53 

PYRROLIDINE 

QUARTZ 

QUINOLINE 

QUINONE 

RADON 

RESOURCINOL 

RICIN 

RICININE 

ROSIN 

ROTENONE 

RUBIDIUM 

RUTHENIUM 

SAFROLE 

SALICYLICANILIDE 

SAPONINS 

SARIN 

SILANES 

SILICA 

SILICON CHLORIDE 

SISAL 

SODIUM CHLORATE 

SODIUM ETHYL XANTHATE 

SODIUM HYDROXIDE 

SODIUM NITROPRUSSIDE 

SODIUM PEROXIDE 

SOMAN 

SORBIC ACID 

SPARTEINE 

STANNANE 

STRONTIUM 

STROPHANTHIN 

STRYCHNINE 

STYRENE OXIDE 

SULFUR DIOXIDE 

SULFUR TRIOXIDE (ALPHA) 

SULFURIC ACID 

SULFUROUS ACID 

TABUN 

TAR, DEHYDRATED 

TAR, LIQUID 

TARTARIC ACID 

TELLURIUM 

TETRACHLORONAPHTHALENE 

TETRACHLOROSILANE

POLLUTANTS IV, cont. 

TETRAETHYL PYROPHOSPHATE 

TETRAETHYLTHIURAM SULFIDE 

TETRAHYDROFURAN 

TETRAHYDRONAPHTHALENE 

TETRANITROMETHANE 

TETRYL 

THALLIUM 

THEBAINE 

THEOPHORIN 

THIOCETIC ACID 

THIOGLYCOLIC ACID 

THIOGLYCOLLATES 

THIONYL CHLORIDE FLUORIDE 

THIONYL FLUORIDE 

THIOPHOSPHORYL FLUORIDE 

THIOSEMICARBAZONE 

THORIUM 

TIGLIC ACID 

TITANIUM TETRACHLORIDE 

TOLUENE 

TOXAPHENE 

TREMETOL 

TRI-o-CRESYL PHOSPHATE 

TRICHLOROACETYL CHLORIDE 

TRICHLOROSILANE 

TRIFLUORONITROSOMETHANE 

TRIISOBUTYLALUMINUM 

TRIMETHYLAMINE 

TRINITROANISOLE 

TRINITROTULUENE 

TRISODIUM PHSOPHATE 

TRITIUM 

TUMERIC 

TURPENTINE 

o-TOLUIDINE 

p-THOIXENE 

ULTRAVIOLET RADIATION 

UNDECANAL 

URANIUM 

URIC ACID 

URUSHIOL 

VANADIUM 

VARNISH 

VINYL CHLORIDE 

54 

VINYL ETHER 

VINYLTRICHLOROSILANE 

WARFARIN 

WELDING FUMES 

WHISKY 

XENON 

XYLIDINE 

m-XYLYL BROMIDE 

m-XYLYL CHORIDE 

m-XYLYNE 

YOHIMBINE 

ZIRCONIUM

THE LIQUITROPHIC PHILOSOPHY 

In the development of a nutritional science we find that the body does 

indeed need vitamins, enzymes, coenzymes and a multitude of other 

factors to survive, including protein, carbohydrates, fats, water, air, and 

exercise. In the field of homeopathy we often deal with just subtle 

energies, but homeopathy need not always be so dilute. Many 

homeopathics can be utilized in low concentrations at mother tinctures 

of 1x, 2x, 3x, or 4x to supply chemical properties to the system for 

chemical effects. 

The Dr. Recommends’ Liquitrophics remedies supply the vitamins, 

minerals, enzymes, alkaloids and hormones needed by the body to 

regulate biological activities. 

The Liquitrophics remedies are not in pill form, but in liquid form to 

maximize the surface area and to trigger the digestive system for 

absorption at the point in which it works best; the mouth. Inside the 

nasal pharynx area are many nerve structures running to the brain that 

help trigger the digestive system for maximum absorption and utilization 

of the remedy. 

The liquid formulation of these remedies maximizes their effectiveness. 

This means less can be used in much safer dosages. The Dr. 

Recommends’ Liquitrophics remedies are developed to be safe for 

children within their specific context and are quality controlled within 

the QQC TM standards. 

55

LIQUITROPHIC REMEDIES 

ADRENO LIQUITROPHIC (4 fl. oz.) 


Indication: Weak adrenal glands, hypoadrenia 

Ingredients: Panax Quinquefolium 2x. Sarcodes: Adrenal, Spleen, 

Pantothenic Acid, Lobelia cardinalis, Rosa canina 3x. Coffea cruda, 

Paullinia sorbilis 3x, 6x. Ephedra vulgaris 3x, 6x, 12x. Ascorbic acid, 

Magnesia Phosphorica, Adrenalinum 4x. Arachidonic Acid 5x, 12x, 30x, 

60x, 1000x. Sarcodes: Pituitary, Hypothalamus 6x. 

Adrenocorticotrophin 6x, 12x, 30x. 

AMINO LIQUITROPHIC (4 fl. oz.) 


Indication: Supplies amino acids and minerals 

Ingredients: Panax quinquefolium, Hydrocotyle asiatica, Polygonum 

punctatum, Fucus disticus, Undaria pinnatifida, Gigartina papillata, 

Porphyra, Arame, Rhodymenia, Alaria esculenta 2x. 

ARTHRO LIQUITROPHIC (4 fl. oz.) 


Indication: Connective tissue repair, joint strain or sprains 

Ingredients: Calendula officinalis, Echinacea purpurea, Symphytum 

officinale, Rhododendron chrysanthum 3x. Shark and Bovine Muscle, 

Ligament, Cartilage 3x, 6x. Ruta graveolens 4x. Collagen, Elastin 4x, 

12x, 60x, 100x, 500x. Silicea 5x, 6x, 12x. Hypericum perforatum, 

Euphrasia officinalis, Aceticum Acidum, Arnica montana 6x. Glycine, 

Alanine, Serine, Proline 6x, 12x, 30x, 60x. Formica rufa 20x. 

B LIQUITROPHIC (4 fl. oz.) 


Indication: Mental depression, pellagra, vaso constriction 

Ingredients: Hordeum vulgare, Saccharomyces cerevisiae, Angelica 

archangelica 3x. Sarcodes: Liver, Heart 3x. Vitamins: B1 - B20, 3x, 4x, 

12x, 30x, 60x, 100x. Beta vulgaris, Raphanus sativus 4x, 5x, 6x, 16x. 

Natrum Pyruvate 6x, 12x, 30x. 

C LIQUITROPHIC (4 fl. oz.) 


Indication: Supplies Vitamin C, infection resistance 

Ingredients: Citrus limonum, Malpighia punicifolia, Rosa canina, 

Solanum tuberosum 1x. Calcium Ascorbate, Citrus aurantium, Bone 

Marrow 2x. Agaricus bisporus, Petroselinum sativum, Capsicum 

Annuum 3x. Ascorbatase 6x. 

56

CARDIO LIQUITROPHIC (4 fl. oz.) 


Indication: Heart repair, infarction risk 

Ingredients: Crataegus Oxyacantha, Plantago major, Kali Muriaticum, 

Kali Phosphoricum 3x. Cytisus scoparius 4x, 6x, 12x, 30x. Sarcodes: 

Thyroidinum, Heart, Vagus Nerve, Cardiac Plexus 4x, 6x, 30x, 100x. 

Cactus grandiflorus 5x. Digitalis purpurea, Natrum Muriaticum, 

Carnitine, Valeriana officinalis, Lecithin 6x. Alanine, Methionine, 

Proline, Leucine 6x, 12x, 30x, 60x. 

DERMA LIQUITROPHIC (4 fl. oz.) 


Indication: Skin repair, psoriasis 

Ingredients: Equisetum arvense, Iris germanica, Berberis vulgaris, 

Mahonia aquifolium 3x. Thuja occidentalis, Nux vomica 6x. Sassafras 

officinale, Chondrus crispus, Mentha piperita 6x, 12x, 30x, 60x, 100x. 

Hypericum perforatum 10x. Mercurius Solubilis, Petroleum 12x. 

Graphites 16x. 

FEM LIQUITROPHIC (4 fl. oz.) 


Indication: Balance the female system 

Ingredients: Rubus idaeus, Dioscorea villosa, Glycyrrhiza glabra, 

Trillium erectum, Liatris spicata 2x. Caulophyllum thalictroides, Ignatia 

amara 6x. Sarcodes: Ovary, Uterus, Mammary, Pituitary, 

Hypothalamus 6x, 12x, 30x. 

G LIQUITROPHIC (4 fl. oz.) 


Indication: Brain repair, dementia, poor memory 

Ingredients: Ginkgo biloba 2x. Glycerinum, Taurine 3x. Brain Sarcodes 

3x, 6x, 12x, 30x, 60x, 100x. Vitamin B2, B6, B15, Niacinamide, Choline, 

PABA, Inositol, Biotin, Folic Acid, Scutellaria lateriflora, Convallaria 

majalis, Tyrosine, Glutamine, Glutamic Acid, Phosphatydl Choline 4x. 

Datura stramonium 8x, 12x. Oxytocin 12x, 30x, 60x, 100x, 500x. 

GLUCO LIQUITROPHIC (4 fl. oz.) 


Indication: Diabetes, hyperglycemia 

Ingredients: Aletris farinosa, Ignatia amara, Rhamnus purshiana, 

Diabatina 2x. Geranium maculatum, Convallaria majalis 3x. 

57

HEMO LIQUITROPHIC (4 fl. oz.) 


Indication: Blood cell repair, anemia 

Ingredients: Ferrum Gluconate, Ferrum Phosphoricum, Ferrum 

Sulphuricum, Ferrum Muriaticum, Trifolium pratense, Panicum 

miliaceum, Fagopyrum esculentum, Beta vulgaris, Panax quinquefolium, 

Hydrocotyle asiatica, Polygonum punctatum, Pyridoxine, 

Cyanocobalamin, Thiamine, Riboflavin, Folicum Acidum 3x, 12, 60, 

500x. Hemoglobin 4x. Sarcodes: Spleen, Bone Marrow, Pituitary, Liver 

6x. Intrinsic Factor 6x, 12x, 30x, 60x. Erythropoietin 6x, 12x, 30x, 60x, 

100x. Tyrosine, Histidine 30x, 60x, 1000x. 

HEMO-A LIQUITROPHIC (4 fl. oz.) 


Indication: Auto-immune disorders 

Ingredients: Cucumis sativus 1x. Phytolacca decandra 2x. Sarcode: 

Thymus 3x. Trifolium pratense, Sarcodes: Adenoids, Tonsils, Appendix 

4x. Vaccinotoxinum 30x, 100x. 

HEPATO LIQUITROPHIC (4 fl. oz.) 


Indication: Liver repair, liver toxicity 

Ingredients: Cucurbita, Beta vulgaris, Raphanus sativus, Arctium, 

Plantago major 2x. Bupleurum, Verbena hastata 2x, 6x. Ascorbicum 

Acidum 3x. Sarcodes: Liver, Gallbladder 3x, 6x, 12x, 30x, 60x, 100x. 

Podophyllum peltatum 4x. Glycine, Methionine, Proline, Cytochrome, 

Flavoprotein, NAD, NADP, Inositol, Choline 5x, 10x, 30x, 100x. Natrum 

Sulphuricum 6x. Natrum Muriaticum 14x. Creatine Phosphokinase, 

Glutamic-oxaloacetic transaminase, Lactic Dehydrogenase 16x, 30x, 60x, 

100x. 

LIENO LIQUITROPHIC (4 fl. oz.) 


Indication: Spleen repair 

Ingredients: Sarcode: Spleen 3x. Quercus robur 4x. Ceanothus 

americanus 6x. Helianthus annuus 6x, 12x. Natrum Muriaticum 6x, 

12x, 30x. Germanium, Arctium lappa, Myeloperoxidase 6x, 12x, 30x, 

60x, 100x. 

58

LIPID LIQUITROPHIC (4 fl. oz.) 


Indication: Fatty acid deficiencies 

Ingredients: Oil from: Canola, Olive, Sesame Seed, Safflower, Sunflower, 

Wheat Germ, Garlic, Carrot, Lemon, Orange, Borage, Linseed (Flax Seed), 

Cod Liver, Lecithin (from Soybean), Lettuce, Evening Primrose, Rose 

Hips, Pumpkin Seed, Cinnamon, Apple Seed, Senna, Myrrh, Barley, 

Apricot Kernel, Currants, Australian Tea Tree, Grape Seed, Hazel Nut. 

LYMPHO LIQUITROPHIC (4 fl. oz.) 


Indication: Lymphatic repair, cleansing 

Ingredients: Echinacea purpurea, Trifolium pratense 2x. Arctium, 

Capsicum annuum, Citrus limonum 3x. Sarcodes: Lymph, Spleen, 

Mammary, Thymus 3x, 6x, 12x, 30x, 60x, 100x. Hydrastis canadensis 

5x. Sarcodes: Adenoids, Tonsils, Appendix 5x, 12x, 30x, 60x, 100x. 

NEO LIQUITROPHIC (4 fl. oz.) 


Indication: Degenerative tissue 

Ingredients: Vinca minor, Carduus marianus, Phytolacca decandra, 

Plantago major 2x. Sanguinaria canadensis, Viscum album, Amygdala 

amara 3x. Carduus benedictus, Taxus baccata 3x, 6x, 12x, 30x, 60x, 

100x. Rhamnus cathartica, Glycyrrhiza glabra 6x. 

NEPHRO LIQUITROPHIC (4 fl. oz.) 


Indication: Kidney repair, detoxification of protein waste 

Ingredients: Hydrangea arborescens 2x. Eupatorium purpureum, 

Pareira brava, Pisum sativum, Taraxacum officinale 3x. Natrum 

Phosphoricum 3x, 6x, 12x, 30x, 60x, 100x. Kali Carbonicum, Natrum 

Nitricum 4x, 6x, 12x, 30x, 60x, 100x. Berberis vulgaris, Uva ursi, 

Sarcodes: Kidney, Bladder 6x, 12x, 30x, 60x, 100x, 500x. Urea, 

Ammonium, Rennin, Aldosterone 24x, 40x, 60x, 100x. 

59

OSTEO LIQUITROPHIC (4 fl. oz.) 


Indication: Bone repair, cold & flu 

Ingredients: Bone Meal, Liquid Calcium, Lactuca sativa 3x, 6x, 12x, 60x, 

100x, 1500x. Calcarea Fluorica, Calcarea Sulphurica, Calcarea 

Phosphorica, Calcarea Muriatica, Calcarea Carbonica, Manganum 

Metallicum, Magnesium Metallicum, Equisetum arvense, Juglans nigra, 

Vitamin D, D2, D3, A, F 4x, 8x, 12x, 60x, 100x. Niccolum Metallicum 

5x, 12x, 30x, 60x, 100x. Osteoclasts, Osteoblasts 6x, 12x, 30x, 60x, 

100x. Thyrocalcitonin 6x, 12x, 30x, 60x, 100x, 500x, 1000x. Sarcodes: 

Bone, Thyroidinum, Parathyroid, Liver, Kidney, Skin 6x, 30x, 60x, 100x, 

1000x. Fluorine, Molybdenum 12x, 30x, 100x. 

OXY LIQUITROPHIC (4 fl. oz.) 


Indication: Oxygenator and energizing aid 

Contraindication: Flower, yeast, bee pollen allergies 

Ingredients: Bee Pollen, Flower Pollen, RNA-DNA from Yeast 2x. 

Amygdala amara, Laminaria, Medicago sativa, Symphytum officinale 3x. 

Vitamins B12-B18, Chelated Zinc 6x. Oxytocin, Carbonic Anhydrase, 

Hemoglobin, Taurine 6x, 12x, 60x, 100x. 

PITUI LIQUITROPHIC (4 fl. oz.) 


Indication: Pituitary repair, Assists in detox 

Ingredients: Amygdala amara 3x. Cimicifuga racemosa, Sarcode: 

Hypothalamus 3x, 6x, 12x, 30x. Sarcodes: Pituitary Anterior, Pituitary 

Posterior 4x. Caulophyllum thalictroides 6x. Arginine, Lysine, Ornithine 

6x, 12x, 30x. Adrenocorticotrophin 6x, 12x, 30x, 60x, 100x. 

PROPEPSIA LIQUITROPHIC (4 fl. oz.) 


Indication: Stimulates and balances digestive enzyme release 

Ingredients: Pancreatinum 2x. Bromelain, Papain, Coriandrum sativum, 

Cinnamomum, Eugenia caryophyllata, Berberis vulgaris, Herbal Bitters, 

Mentha piperita, Ananas comosus 3x. Sarcodes: Parotid, Stomach, 

Pancreas, Liver, Small and Large Intestine, Vagus Nerve 6x. 

Pancreozymin-cholecystokinin, Lysozyme, Pepsinogen, Trypsinogen, 

Chymotrypsin, Lipase, Amylase, Cellulase, Protease, 6x, 12x, 30x, 60x, 

100x, 500x. 

60

PULMO LIQUITROPHIC (4 fl. oz.) 


Indication: Lung repair 

Ingredients: Eucalyptus globulus 2x. Sarcode: Lung 3x. Adrenalinum 

4x. Sanguinaria canadensis 6x. Carbon Dioxide, Ferrum Metallicum, 

Zincum Metallicum, Oxygen, Carbonic Anhydrase, Verbascum thapsus, 

Curare 6x, 12x, 30x, 60x, 100x. Belladonna 12x. 

SEROTO LIQUITROPHIC (4 fl. oz.) 


Indication: Parkinsonian symptoms, depression 

Contraindication: High blood pressure 

Ingredients: Musa paradisiaca, Medicago sativa, Scutellaria lateriflora, 

Valeriana officinalis, Nerium odorum, Magnesia Phosphorica, GABA, 

Choline Chloride, Inositol, Niacinum, Pyridoxine 3x, 6x, 12x, 30x, 60x, 

100x. Serotonin, Dopamine 4x, 12x, 60x, 100x. 5-Hydroxy-L- 

Tryptophan, Niacinamide 6x, 12x, 30x, 60x, 100x. Amygdala amara 30x, 

100x. 

THYMO LIQUITROPHIC (4 fl. oz.) 


Indication: Thymus repair 

Contraindication: Disease involving excess white blood cell count 

Ingredients: Sarcode: Thymus 3x. Thymol, Natrum Muriaticum 6x. 

Phytolacca decandra, Arctium lappa 6x, 12x, 30x. 

THYRO LIQUITROPHIC (1 fl. oz.) 


Indication: Thyroid repair 

Contraindication: Hyperthyroid conditions 

Ingredients: Olive Oil, Canola Oil, Sesame Oil. Thyroidinum 3x, 5x, 6x, 

12x, 30x, 100x. Lac defloratum 4x, 6x, 8x. Fucus vesiculosus 6x, 12x, 

30x. Molybdenum 8x. Plumbum Metallicum, Mercurius Vivus, 

Argentum Metallicum, Platinum Metallicum, Alumina, Bismuthum 

Metallicum, Carboneum, Selenium Metallicum, Stannum Metallicum, 

Silicea, Sulphur 30x, 60x, 100x. 

61

LIQUITROPHIC INSTRUCTION 

� Liquitrophics may be taken with meals, although they should not 

be mixed with piping hot foods over 106 degrees F. 

� Refrigerate after opening. 

� Liquitrophics and homeopathics should be taken 20 minutes 

apart. 

� Do not store Liquitrophics in sunlight. 

� Liquitrophics may be taken at the same time with other 

Liquitrophics. The exception to this would be that Lipid 

Liquitrophic and Thyro Liquitrophic should not be mixed with 

other homeopathics or Liquitrophics. 

CAUTION: Alcohol sensitivities: If a person is sensitive to alcohol, put 

the dosage into a 3 oz. glass of warm water. Allow one minute for the 

alcohol to evaporate. 

By following these guidelines, you will give the remedies the greatest 

opportunity to succeed. 

62

AMINO ACIDS 

ALANINE (L-ALANINAMIDE) 

ARGININE (L-ARGININAMIDE) 

ASPARAGINE (NA-T-BOC-N-Y-XANTHYL-L-ASPARAGINE) 

ASPARTIC ACID (L-ASPARTIC ACID AMIDE) 

ASPARTIC ACID (P-NITROPHENYL ESTER) 

CYSTEINE 

GLUTAMIC ACID 

GLUTAMINE 

GLYCINAMIDE 

GLYCINE 

HISTIDINE 

ISOGLUTAMINE 

ISOLEUCINE 

L-LYSINE 

L-METHIONINE 

L-TAURINE 

LEUCINE 

METHIONINE 

N-CBZ-EZ-AMINO-N-CAPROIC ACID 

N-CBZ-D-3-(2-NAPHTHYL) ALANINE 

N-CBZ-L-HOMOSERINE 

N-CBZ-Y-AMIN0-N-BUTYRIC ACID 

N-T-BOC-L-HOMOSERINE 

N-T-BOC-Y-AMINOBUTYRIC ACID 

NORLEUCINE 

NORVALINE 

ORNITHINE 

PHENYLALANINE 

PROLINE 

PYROGLUTAMIC ACID 

SARCOSINE 

SERINE 

STATINE 

THREONINE 

TRYPTOPHAN 

TYROSINE 

VALINE 

63

LIPIDS 

Diglycerides 

Fatty Acid Anhydrides 

C 2:0 Acetic 

C 4:0 Butyric 

C 6:0 Caproic 

C 8:0 Caprylic 

C 10:0 Capric 

C 12:0 Lauric 

C 14:0 Myristic 

C 16:0 Palmitic 

C 17:0 Heptadecanoic 

C 18:0 Stearic 

C 18:1, cis-9 Oleic 

C 18:1, trans-9 Elaidic 

C 18:2, cis-9, 12 Linoleic 

C 20:0 Arachidonic 

C 22:1, cis-11 11-Eicosenoic 

C 22:0 Behenic 

C 6:0 Dicaproin, 1,3 isomer 

C 8:0 Dicaprylin, 1,2-, 1,3-and mixed isomers 

C 10:0 Dicaprin, 1, 2-, 1, 3- and mixed isomers 

C 12:0 Dilaurin, 1, 2-, 1, 3- and mixed isomers 

C 14:0 Dimyristin, 1, 2-, 1, 3- and mixed isomers 

C 15:0 Dipentadecanoin, 1, 3-isomer 

C 16:0 Dipalmitin, 1,2-, 1,3- and mixed isomers 

C 18:0 Disteaarin, 1, 2-, 1, 3- and mixed isomers 

C 18:1, cis-9 Diolein, 1,2- 1,3- and mixed isomers 

C 18:1, cis-9, C2:0 1-Oleoyl-2-Acetyl 

C 18:1, trans-9 Dielaidin, 1,3-isomer 

C 18:2, cis-9, 12 Dilinolein, 1,3-isomer 

C 20:0 Diarachidin, 1,3-and mixed isomers 

C 20:1, cis-11 Di-11-Eicosenoin, mixed isomers 

C22:1, cis-13 Dierucin, mixed isomers 

64

LIPIDS, cont. 

Monoglycerides 

C 8:0 1-Monocapryloyl-rac-glycerol 

C 10:0 1-Monodecanoyl-rac-glycerol 

C 12:0 1-Monolauroyl-rac-glycerol 

C 14:0 1-Monomyristoyl-rac-glycerol 

C 16:0 1-Monopalmitoyl-rac-glycerol 

C 16:1, cis-9 1-Monopalmitoleoyl-rac-glycerol 

C 18:0 1-Monostearoyl-rac-glycerol 

C 18:1, cis 9 1-Monooleoyl-rac-glycerol 

C 18:1, trans-9 Monoelaidin 

C 18:2, cis-9, 12 1-Monolinoleoyl-rac-glycerol 

C 18:3, cis-9,12,15 1-Monolinoleoyl-rac-glycerol 

C 20:1, cis-11 Mono-11-eicosenooin, 1-isomer 

C 22:1, cis-13 Monoerucin, 1-isomer 

65

Lipids, cont. 

Triglycerides 

C 2:0 Triacetin 

C 4:0 Tributyrin 

C 6:0 Tricaproin 

C 8:0 Tricaprylin 

C 9:0 Trinonanoin 

C 10:0 Tricaprin 

C 12:0 Trilaurin 

C 13:0 Tritridecanoin 

C 14:0 Trimyristin 

C 14:1, cis-9 Trimyristolein 

C 15:0 Tripentadecanoin 

C 16:0 Tripalmitin 

C 16:1, cis-9 Trielaidin 

C 17:0 Triheptadecanoin 

C 18:0 Tristearin 

C 18:1, trans-9 Trielaidin 

C 18:1, cis-9 Triolein 

C 18:1, cis-6 Tripetroselinin 

C 18:2, cis-9, 12 Trilinolelaidin 

C 18:3, cis-9, 12, 15 Trilinolenin 

C 19:0 Trinonadecanoin 

C 20: Triarachidin 

C 20:1, cis-5, 8, 11, 14 Triarachidonin 

C 22:0 Tribehenin 

C 22:1, cis-13 Trierucin 

C 24:1, cis-15 Trinervonin 

66

HORMONES 

ACETYL CHOLINASE 

ACETYL CHOLINE 

ADRENAL PEPTIDE E 

ADRENALIN 

ADRENOCORTICOTROPIC HORMONE (ACTH: CORTICOTROPIN A) 

ALDOSTERONE 

AMASTATIN 

ANGIOTENSIN (CONVERTING ENZYME INHIBITOR) 

ANGIOTENSIN I 

ANGIOTENSIN II (HYPERTENSIN II) 

ANGIOTENSIN III INHIBITOR 

ANGIOTENSINOGEN (FRAGMENT) 

ANTI-PAIN 

ANTI-REPRODUCTIVE TRIPEPTIDE 

ATRIOPEPTIN I 

ATRIOPEPTIN II 

ATRIOPEPTIN III 

BEAUVERICIN 

BRADYKININ 

BRADYKININ POTENTIATOR C 

B-CASOMORPHIN 

B-LIPOTROPIN FRAGMENTS 

BRADYKININ POTENTIATOR B 

CAERULEIN 

CALCITONIN (THYRO) 

CHOLECYSTOKININ 

CHYMOSTATIN 

CORTICOTROPIN RELEASING FACTOR 

DERMORPHIN 

DYNORPHIN A (PORCINE) 

CYNORPHIN B (PORCINE) 

ELASTIN CHEMOTACTIC FRAGMENT 

ELEDOISIN 

ENKEPHALINAMIDE 

EPINEPHRINE 

ERYTHROPOIETIN 

ESTROGEN 

a-ENDORPHIN 

GALANIN 

GASTRIC INHIBITORY POLYPEPTIDE 

GASTRIN 

GASTRIN RELEASING PEPTIDE 

GASTRIN I FRAGMENTS 

GASTRIN II 

67

HORMONES, cont. 

GLUCAGON 

GLUTATHIONE 

GROWTH HORMONE 

GROWTH HORMON RELEASING FACTOR 

INSULIN 

KALLIDIN 

KATACALCIN 

KEMPTIDE 

KENTSIN 

KETOSTEROIDS (ALL) 

KYOTORPHIN 

L-ALANYLGLYCYL-L-SERYL-L-GLUTAMIC ACID 

L-METHIONYL-L-LEUCYL-L-PHENYLALANINE 

L-TYROSYLGLYCYLCLYCINE 

L-VALYLGLYCYL-L-SERYL-L-GLUTAMIC ACID 

LEUCINE ENKEPHALIN-LYS 

LEUPEPTIN 

LEUTINIZING HORMONE 

LEUTINIZING RELEASING HORMONE 

METHIONINE ENKEPHALINE 

MINERAL CORTICOID 

MORPHICEPTIN 

MOTILIN 

a-MELANOCYTE STIMULATING HORMONE 

a1-MATING FACTOR 

(D-TRP2)-METHIONINE ENKEPHALIN 

N-ACETYL-L-METHIONYL-L-LEUCYL-L-PHENYLALANYL-L-METHIONINE 

N-FORMYL-L-METHIONYL-L-LEUCYL-L-PHENYLALANINE METHYL 

N-FORMYL-L-METHIONYL-L-LEUCYL-L-TYROSINE 

N-FORMYL-L-METHIONYL-L-PHENYLALANYL-L-LYSINE N-FORMYL 

N-FORMYL-L-NORLEUCYL-L-LEUCYL-L-PHENYLALANINE 

N-T-BOC-L-LEUCYL-L-PHENYLALANINE 

N-T-BOC-L-METHIONYL-L-LEUCYL-L-PHENYLALANINE 

N-T-BOC-L-METHIONYL-L-LEUCYL-L-TYROSINE 

NEOENDORPHIN 

NERVE GROWTH FACTOR 

NEUROMEDIN C 

NEUROTENSIN 

NOREPINEPHRINE 

a-NEOENDORPHIN 

OXYTOCIN 

PANCREATIC POLYPEPTIDE 

PANCREOZYMIN 

PARATHYROID HORMONE 

68

PEPTIDE YY 

PITUITARY DIURETIC HORMONE (POSTERIOR) 

PITUITARY RELEASE (ANTERIOR) 

PRESSINOIC ACID 

PROCTOLIN 

PROENKEPHALIN 

PROGESTERONE 

PROLACTIN 

RENIN 

RENIN INHIBITOR 

SCHIZOPHRENIA RELATED PEPTIDE 

SECRETIN 

SOMATOSTATIN 

SOMATOSTATIN 25 

SOMATOSTATIN 28 

SYNDYPHALIN-20 

TESTOSTERONE 

THYMOPOIETIN 32-36 

THYMOSIN 

THYROCALCITONIN 

THYROID STIMULATING HORMONE 

VAL-GLY-VAL-ALA-PRO-GLY 

VASOPRESSIN 

VASOTOCIN 

XENOPSIN 

YEAST a-FACTOR 

69

HOMRONES/BIOACTIVE PEPTIDES 

Adrenocorticotropic Hormone (ACTH: Corticotropin A) 

Angiotensin I 

Angiotensin II (Hypertensin II) 

Angiotensin III 

Angiotensin III Inhibitor 

Angiotensin-Converting Enzyme Inhibitor (pGlu-Trp-Pro-Arg-Pr9o-Gin- 

lie-Pro-Pro) 

Angiotensinogen (Fragment 1-14) 

Renin 

Bradykinin (Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg) 

Bradykinin Potentiator B (pGlu-Gly-Leu-Pro-Pro-Arg-Pro-Lys-11e-Pro- 

Pro) 

Bradykinin Poetntiator C (pGlu-Gly-Leu-Pro-Pro-Gly-Pro-Pro-11e-Pro- 

Pro) 

CHEMOTACTIC PEPTIDES 

N-Acetyl-L-Methionyl-L-Lefucyl-L-Phenylalanine 

L-Alanylglycyl-L-Seryl-L-Glutamic Acid (Eosinophil chemotactic factor of 

anaphylaxis) 

N-t-BOC-L-Methionyl-L-Leucyl-L-Phenylalanine (Chemotactic peptide 

antagonist) 

N-t-BOC-L-Phenylalanyl-D-Leucyl-L-Phenylalanyl-D-Leucyl-L- 

Phenylalanin 

(Chemotactic peptide inhibitor) 

N-Formyl-L-Methionyl-L-Leucyl-L-Phenylalanine Methyl Ester (A potent 

chemotactic peptide for human blood monocytes) 

N-Formyl-L-Methionyl-L-Leucyl-L-Phenylalanyl-L-Lysine (Acetate salt) 

N-Formyl-L-Methionyl-L-Leucyl-L-Tyrosine (Dicyclohexylammonium salt) 

N-Formyl-L-Norleucyl-L-Leucryl-L-Phenylalanine (Chemotactic peptide) 

N-Formyl-L-Norleucyl-L-Leucyl-L-Phenylalanyl-L-Tyrosine 

L-Methionyl-L-Leucyl-L-Phenylalanine (Acetate Salt – Exhibits very weak 

chemotactic properties) 

Val-Gly-Val-Ala-Pro-Gly (Elastin chemotactic fragment) 

L-Valylglycyl-L-Seryl-L-Glutamic Acid (Esinophil chemotactic factor of 

anaphylaxis) 

Dynorphin A (Porcine) 

Dynorphin B (Porcine) 

a-Endorphin 

Leucine Enkephalin 

Leucine Enkephalin-Lys 

Enkephalinamide 

Methionine Enkephaline (Tyr-Gly-Gly-Phe-Leu-Lys) 

[D-Trp 2 ]-Methionine Enkephalin 

70

Proenkephalin 

Syndyphalin 

Syndyphalin-20 

L-Tyrosylglycylglycine 

ENZYME INHIBITORS 

Amastatin 

Angiotensin-Converting Enzyme Inhibitor 

Antipain 

Chymostatin 

Leupeptin 

GASTROINTESTINAL PEPTIDES 

Caerulein 

Cholecystokinin 

Galanin 

Gastric Inhibitory Polypeptide 

Gastrin 

Gastrin I Fragments 

Gastrin II (Sulfated) 

Gastrin Releasing Peptide (Porcine) 

Glucagon (Crystalline) 

Pancreatic Polypeptide 

Pancreozymin 

Peptide YY 

Secretin 

Growth Hormone Releasing Factor (1-44) 

a-Melanocyte Stimulating Hormone 

Neurotensin 

OPIOID PEPTIDES 

Adrenal Peptide E 

B-Casomorphin 

Dermorphin 

Kyotorphin 

Morphiceptin 

Oxytocin 

Pressinoic Acid 

Vasopressin 

Vasotocin 

Somatostatin 

Somatotstatin 25 

71

Somatostatin 28 (Fragment 1-14) 

MISCELLANEOUS 

Amastatin 

Antipain 

Beauvericin 

Calcitonin 

Cholecystokinin 

Corticotropin Releasing Factor 

Elastin Chemotactic Fragment 

Eledoisin 

Erythropoietin 

Glucagon 

Glutathione 

Insulin 

Katacalcin 

Kentsin 

Neuromedin C 

Pancreozymin 

Proctolin 

Proenkephalin 

Thymosin a 

Thyrocalcitonin 

Xenopsin 

72

ENZYMES 

ACETYL CHOLINE ESTER 

ACETYLESTERASE 

ACID MALTASE – POMPE’S DISEASE 

ACID PHOSPHATASE 

ADENOSINE 5’-DIPHOSPHATE 

ALKALINE PHOSPHATASE 

ALAKALINEPROTEASE 

ALDOASE 

ALPHA 1, 4 GLUCOSIDASE – POMPE’S DISEASE 

AMINO ACID DECARBOXYLASES 

AMINO ACID OXIDASE 

AMINOBUTYRIC ACID TRANSAMINASE 

AMYLO-1, 6 GLUCOSIDASE – CORI’S DISEASE 

ANGIOTENSIN-CONVERTING ENZYME INHIBITOR 

ARGINASE 

ARGININE DECARBOXYLASE 

ASCORBATE OXIDASE 

ASPARAGINASE 

ASPARTIC ACID DECARBOXYLASE 

ATPase 

a-AMYLAST 

b-AMYLASE 

BILE ACID DEHYRDROGENASE 

BUTYL CHOLINESTERASE 

CALCULASE 

CANDIDA PSEUDOTROPICALIS 

CANDIDA UTILIS 

CARBONIC ANHYDRASE 

CARBOXYPEPTIDASE A 

CARNITINE PALMITOYLTRANSFERASE –MYOPATHY 

CAROBXYPEPTIDASE B 

CATALASE 

CELLULASE 

CHOLESTEROL 

OXIDASE 

CHOLINE KINASE 

CHOLINESTERASE, ACETYL 

CHLOROPEROXIDASE 

CHOLESTEROL ESTERASE 

CHOLINE ACETYLTRANSFERASE 

CHOLINE OXIDASE 

CHOLINESTERASE, BUTYRYL 

CHYRO TRYPSIN 

COENZYME A DEHYDROGENASE 

73

ENZYMES, cont. 

COLLAGENASE 

CORTISONE REDUCTASE 

CREATINASE 

CREATININASE 

CREATININE PHOSPHOKINASE 

CYTOCHROME b2 

CYTOCHROME C REDUCTASE 

a-CHYMOTRYPSIN 

DEOXYRIBONUCLEASE (ATP DEPENDENT) 

DEOXYRIBONUCLEASE 1 

DEOXYRIBONUCLEASE 2 

DEOXYRIBONUCLEIC ACID LIGASE 

DEOXYRIBONUCLEIC ACID POLYMERASE 

DEXTRANASE 

DNA LIGASE 

DNA POLYMERASE 

DOPAMINE B-MYDROXYLAST 

ELASTASE 

ENTEROKINASE 

FORMALDEHYDE DEHYDROGENASE 

FUCOSE DEHYDROGENASE 

GABASE 

GLUTAMINASE 

GLUTATHIONE PEROXIDASE 

BLUATHIONE REDUCTASE 

GLUCOSE DEHYDROGENASE 

GLUTAMIC DECARBOXYLASE 

GLUTAMIC DEHYDROGENASE 

GLYCEROL DEHYDROGENASE 

GLYCOGEN PHOSPHORYLASE 

GLYCOGEN SYNTHETASE 

HISTAMINE 

HISTIDASE 

HYALURONIDASE 

HYDROXYPYRUVATE REDUCTASE 

HYDROXYSTEROID DEHYDROGENASE 

INVERTASE 

ISOAMYLASE 

ISOCITRATE LYASE 

ISOMALTASE 

LACTASE 

LACTATE DEHYDROGENASE 

LACTATE 2-MONOOXYGENASE 

74


LACTIC DEHYDROGENASE 

LACTOPEROXIDASE 

LDH 

LECITHINASE A 

LECITHINASE B 

LECITHINASE C 

LECITHINASE D 

LEUCINE DEHYDROGENASE 

LIPASE 

LIPOXIDASE 

LYSIN 

LYSINE DECARBOXYLASE 

LYSOZYME 

LYTIC ENZYMES 

MALATHION HYDROLASE 

MALTASE 

MERCURIPAPAIN 

MONOAMINE OXIDASE 

MYLEO PEROXIDASE 

MYOPHOSPHORYLASE – McARDLE’S DISEASE 

MYOSIN 

NADASE 

NEURAMINIDASE 

NUCLEASE 

OTNIHINE DECARBOXYLASE 

OXALATE OXIDASE 

PANCREATIN 

PANCREOZYMIN 

PAPAIN 

PARATHION HYDROLASE 

PECTINASE 

PECTOLYASE 

PENICILLINASE 

PEP CARBOXYLASSE 

PEPSIN 

PEPSINOGEN 

PEPTIDASE 

PEROXIDASE 

PHOSPHATASE, ACID 

PHOSPHODIESTERASE 

PHOSPHOFRUCTOKINASE – MYOPATHY 

PHOSPHOLIPASE A2 

PHOSPHORYLASE 

75


PHYTASE 

PROSTAGLANDID DEHYDROGENASE 

PROTEASE 

PYRUVATE DEHYDROGENASE 

PYRUVATE KINASE 

PYRUVATE OXIDASE 

PYTALIN 

TRYPSIN 

RENIN 

RENNIN 

RIBONUCLEASE 

SACCHARASE 

SBP BROMELAIN PAPIN 

STEROID DEHYDROGENASE 

SUCRASE 

TRYPSIN 

TRYPSINOGEN 

TRYPTOPHAN 

TYROSINASE 

URICASE 

VANILMANDELIC ACID DEHYDROGENASE 

VITAMIN C ASE 

XANTHINE OXIDASE 

76

THE ANODYNE PHILOSOPHY 

Anodyne is the medical word for a remedy used to treat pain 

conditions. The neurology of pain involves many sensory neurons and 

their ability to project neurological signals through the nervous 

system to the brain, which then perceives these signals as pain. The 

physiology of pain is akin to the physiology of neurology and 

perception. Pain results when there is an over or under balance in the 

neurons of any area resulting in an energetic overload. 

The Dr. Recommends’ anodyne remedies are formulated to help in a 

wide variety of pain conditions. They are not designed to cover up the 

pain, nor are they designed as pain killers. They are designed to help 

in healing the factors behind the pain and to stimulate the organism 

into a healing process, thereby reducing the amount of pain through 

natural means. Anodyne formulas give us a broad-based collection of 

easy-to-use remedies to help many types of pain conditions in the 

body and are quality controlled within the QQC TM guidelines. 

Pain is not the enemy; pain is indeed the messenger of a problem 

and must not be fought against. It is the purpose of homoeopathy to 

work with the pain. 

If pain persists, it is a further indication that there is a serious 

underlying condition and the patient should be referred to a 

professional who can treat the patient effectively. 

77

ANODYNE REMEDIES 

ABDOMINAL ANODYNE (1 fl. oz.) 


Indication: Cramping, Pre-appendicitis 

Ingredients: Ferrum Metallicum, Chamomilla 3x. Bismuthum 

Metallicum, Borax 4x. Lycopodium clavatum 5x. Carbo Vegetabilis, Solar 

Plexus, Vagus Nerve, Bovine Stomach Tissue, Natrum Sulphuricum 6x, 

12x, 30x, 60x, 100x. Bromium 7x. Sulphur 8x, 30x, 60x. Muriaticum 

Acidum, Platinum Metallicum, Alumen 12x, 30x, 60x, 100x. Plumbum 

Metallicum, Mercurius Vivus, Nux vomica 30x, 60x, 100x. 

ANODYNE-ACD (1 fl. oz.) 


Indication: Pain from acid conditions 

Ingredients: Natrum Bicarbonate 3x. Full spectrum Fatty Acids, Coca, 

Ferrum Metallicum 5x. Antimonium Tartaricum 6x. Chemoreceptors 6x, 

12x, 30x. Sepia, Muriaticum Acidum 8x, 16x, 30x. Oxalicum Acidum, 

Uricum Acidum 16x, 30x. Endorphins 20x, 60x, 100x. 

ANODYNE-ALK (1 fl. oz.) 


Indication: Pain from alkaline conditions 

Ingredients: Ascorbicum Acidum, Smilax 3x. Coca 5x. Zincum 

Metallicum, RNA-DNA, Magnesium Thiosulfate, Propionaldehyde 6x. 

Chemoreceptors 6x, 12x, 30x. Natrum Bicarbonate 8x, 16x, 30x. 

Causticum, Calcarea Sulphurica, Calcarea Phosphorica, Calcarea 

Magnesia 12x. Endorphins 20x, 60x, 100x. 

ANODYNE-AUTOX (1 fl. oz.) 


Indication: Pain from self-made toxins, injury 

Ingredients: Smilax 3x. Symphytum officinale 4x. Arnica montana 4x, 

10x, 30x. Calendula officinalis 5x, 15x, 30x. Isotonic Plasma 6x, 20x. 

Mechanoreceptors 6x, 12x, 30x. Aurum Metallicum, Carbo Animalis 12x. 

Endorphins, Gate Receptors (Spine & Brain) 20x, 60x, 100x. 

Vaccinotoxinum 60x, 100x, 500x, 1000x. 

78

ANODYNE-C (1 fl. oz.) 


Indication: Pain where cold improves 

Ingredients: Pulsatilla 4x. Natrum Sulphuricum 6x. Dulcamara 6x, 12x, 

30x. Ferrum Metallicum 6x, 12x, 30x, 100x. Sarcodes: Temperature 

Sensor Nerve Cells 6x, 12x, 30x, 60x, 100x. Arsenicum Metallicum 8x. 

Rhododendron chrysanthum 12x. Echinacea purpurea, Lachesis mutus 

12x, 30x, 100x. Aluminium Metallicum, Aurum Metallicum, Bismuthum 

Metallicum, Borax, Plumbum Metallicum, Silicea 16x, 20x, 50x, 100x. 

ANODYNE-ELC (1 fl. oz.) 


Indication: Pain provoked by exposure to electric or energetic fields, 

television, microwaves, etc. 

Ingredients: Euphrasia officinalis, Pilocarpus 3x. Agate 4x, 5x, 6x. 

Cuprum Metallicum 6x, 12x. Electromagnetic Nerve Receptors 6x, 12x, 

30x, 60x, 100x. Full spectrum EMR, Full spectrum magnetic oscillations 

6x, 12x, 30x, 60x, 100x, 500x, 1000x. Glonoine 12x, 30x. Corallium 

Nigra 30x. 

ANODYNE-NT (1 fl. oz.) 


Indication: Pain where no touch improves 

Ingredients: Zincum Metallicum 3x. Selenium Metallicum 4x, 6x, 30x, 

100x. Bryonia 5x. Nux vomica 6x. Zincum Metallicum 6x, 12x, 30x, 

60x. Sarcodes: Kruski Cells (Pressure Sensors) 6x, 12x, 30x, 60x, 100x. 

Silicea 6x, 12x, 30x, 100x. Arsenicum Album, Gelsemium sempervirens, 

Plumbum Metallicum, Lachesis mutus 8x, 12x, 30x. 

ANODYNE-T (1 fl. oz.) 


Indication: Pain where touch improves 

Ingredients: Coffea cruda 3x. Belladonna 4x. Bryonia, Aconitum 

napellus 5x. Spigelia marilandica 6x. Sarcodes: Kruski Cells (Pressure 

Sensors) 6x, 12x, 30x, 60x, 100x. Bismuthum Metallicum, Magnesia 

Phosphorica 12x. Iodium 16x-24x. Borax 16x-30x. 

CEPHALO ANODYNE (1 fl. oz.) 


Indication: Sub-orbital, migraine, temporal headache 

Ingredients: Iris versicolor, Chrysanthemum parthenium, Salix nigra 2x. 

Sanguinaria canadensis 3x. Endorphins 6x, 12x, 30x. Ammonium 

Carbonicum 5x. Silicea, Manganum Metallicum, Cimicifuga racemosa 

6x. Bovine Pituitary Glandular, Antimonium, Arsenicum Metallicum 

12x. Cuprum Metallicum, Graphites, Iodium 16x. 

79

ANODYNE-G (1 fl. oz.) 


Indication: General pain 

Ingredients: Salix alba 3x, 6x. Selenium Metallicum, Zincum Metallicum, 

Vitamins A, C, E 6x. Acetaminophen, Ibuprofen, Acetylsalicylic Acid 

6x-30x. Arsenicum Metallicum, Arum maculatum 6x, 12x, 30x. 

Sarcodes: Major Nerves 6x, 12x, 30x, 60x, 100x. Barium, Mercurius 

Vivus 30x. 

ANODYNE-H (1 fl. oz.) 


Indication: Pain where heat improves 

Ingredients: Kali Carbonicum, Bryonia, Manganum Metallicum 6x. 

Sarcodes: Temperature Sensor Nerve Cells 6x, 12x, 30x, 60x, 100x. 

Sulphur, Zincum Metallicum 6x, 100x. Borax 8x, 12x. Belladonna, Apis 

mellifica, Ruta graveolens, Rhus toxicodendron 12x, 30x. Fluorine, Arnica 

montana 12x, 30x, 100x. Arsenicum Metallicum 12x, 30x, 100x, 500x. 

Mercurius Vivus 30x. 

ANODYNE-M (1 fl. oz.) 


Indication: Pain where motion improves 

Ingredients: Valeriana officinalis 1x. Pulsatilla 2x. Dioscorea villosa 3x. 

Kali Iodatum 4x, 6x, 12x, 70x. Ignatia amara, Oxalicum Acidum 5x. 

Rhus toxicodendron 6x. Phosphorus 8x, 12x, 25x. Cuprum Metallicum 

12x, 30x. Sarcodes: Nerve Sensors of Proprioceptors 12x, 30x, 60x, 100x. 

Silicea 100x, 500x. 

ANODYNE-NM (1 fl. oz.) 


Indication: Pain where no motion improves 

Ingredients: Magnesia Phosphorica 3x, 6x. Bryonia 8x. Manganum 

Metallicum 8x, 12x, 30x. Kreosotum, Nux vomica 9x. Sarcodes: Nerve 

Sensors of Proprioceptors 12x, 30x, 60x, 100x. Platinum Metallicum 20x, 

50x, 100x. Mercurius Vivus 30x, 60x, 100x. 

ANODYNE-NT (1 fl. oz.) 


Indication: Pain where no touch improves 

Ingredients: Zincum Metallicum 3x. Selenium Metallicum 4x, 6x, 30x, 

100x. Bryonia 5x. Nux vomica 6x. Zincum Metallicum 6x, 12x, 30x, 

60x. Sarcodes: Kruski Cells (Pressure Sensors) 6x, 12x, 30x, 60x, 100x. 

Silicea 6x, 12x, 30x, 100x. Arsenicum Album, Gelsemium sempervirens, 

Plumbum Metallicum, Lachesis mutus 8x, 12x, 30x. 

80

ANODYNE-T (1 fl. oz.) 


Indication: Pain where touch improves 

Ingredients: Coffea cruda 3x. Belladonna 4x. Bryonia, Aconitum 

napellus 5x. Spigelia marilandica 6x. Sarcodes: Kruski Cells (Pressure 

Sensors) 6x, 12x, 30x, 60x, 100x. Bismuthum Metallicum, Magnesia 

Phosphorica 12x. Iodium 16x-24x. Borax 16x-30x. 

CEPHALO ANODYNE (1 fl. oz.) 


Indication: Sub-orbital, migraine, temporal headache 

Ingredients: Iris versicolor, Chrysanthemum parthenium, Salix nigra 2x. Sanguinaria 

canadensis 3x. Endorphins 6x, 12x, 30x. Ammonium Carbonicum 5x. Silicea, 

Manganum Metallicum, Cimicifuga racemosa 6x. Bovine Pituitary Glandular, 

Antimonium, Arsenicum Metallicum 12x. Cuprum Metallicum, Graphites, Iodium 16x. 

FACIAL ANODYNE (1 fl. oz.) 


Indication: Facial pain, Symptoms relating to Bell's Palsy 

Ingredients: Salix nigra 3x. Aconitum napellus 4x. Zincum Metallicum, Manganum 

Metallicum, Silicea, Belladonna 6x. Argentum Metallicum 8x. Phosphorus, Chromium 

12x. Trigeminal Nerve 16x, 30x, 60x, 100x, 500x. 

INTERCOSTO ANODYNE (1 fl. oz.) 


Indication: Intercostal neuralgia 

Ingredients: Ruta graveolens 6x, 12x. Arsenicum Album 12x. Intercostal Cartilage, Rib 

Glandular 12x, 30x. Antimonium, Plumbum Metallicum, Rhus toxicodendron 30x. 

LARGE JOINT ANODYNE (1 fl. oz.) 


Indication: Large joint discomfort, knees, elbows, shoulders 

Ingredients: Bryonia 4x. Magnesium Metallicum, Manganum Metallicum, Calcarea, 

Arnica montana, Sulphuricum Acidum 6x. Zincum Metallicum 6x, 12x, 30x, 60x, 100x, 

500x, 1000x. Niccolum Metallicum 8x. Ledum palustre 10x. Sulphur 12x. Ligament, 

Cartilage 12x, 30x. Strontium 20x. 

LUMBO ANODYNE(1 fl. oz.) 


Indication: Low back pain 

Ingredients: Niacinamide 3x. Nux vomica, Atropinum 4x. Rhus toxicodendron 5x. 

Nicotinum 6x. Sarcodes: Kidney, Liver, Lumbar and Sacral Vertebrae, Sciatic and 

Femoral Nerve 6x, 12x, 30x, 60x, 100x. Arnica montana 30x, 100x. 

81

SCIATIC ANODYNE (1 fl. oz.) 


Indication: Sciatic, Low back pain 

Ingredients: Manganum Metallicum 4x, 12x, 30x, 60x, 100x, 1000x. Sarcode: Sciatic 

Nerve 6x, 12x. Magnesia Phosphorica 8x. Atropinum 12x. Aconitum napellus 12x. 

Arsenicum Album 30x. 

SMALL JOINT ANODYNE (1 fl. oz.) 


Indication: Small joint pain in fingers, toes 

Ingredients: Lithium Carbonicum 2X, 12x. Atropinum 4x. Calendula officinalis, 

Nitricum Acidum, Magnesium Metallicum, Manganum Metallicum, Calcarea 6x. 

Rhododendron chrysanthum 6x, 12x, 30x, 60x, 1000x. Zincum Metallicum 6x, 12x, 30x, 

60x, 100x, 500x, 1000x. Niccolum Metallicum 8x. Platinum Metallicum, Sulphur 12x. 

Ligament, Cartilage 12x, 30x. Ammonium Phosphoricum 12x, 30x, 100x. Strontium, 

Plumbum Metallicum 20x. Natrum Sulphuricum, Nux vomica 30x. 

THORACIC ANODYNE (1 fl. oz.) 


Indication: Acute chest pains 

Ingredients: Crataegus oxyacantha, Cactus grandiflorus, Scilla maritima 2x. Kali 

Carbonicum, Kalmia latifolia, Spigelia marilandica 3x. Digitalis purpurea 4x. Arsenicum 

Album, Phosphorus 5x. Manganum Metallicum 6x, 12x, 30x, 60x, 100x. Selenium 

Metallicum 8x. Creatine Phosphokinase, Rennin, Histaminum 12x, 20x, 60x, 100x. 

Zincum Metallicum, Platinum Metallicum 12x, 30x, 60x. 

82

THE COMBINATION PHILOSOPHY 

Combination homeopathy is the most popular type of homeopathy 

used in the world today. Combination ingredients are chosen based on a 

symptomatic picture. Therefore, combinations can be engineered for 

broader based ranges of effectiveness, whereas, singular homeopathics 

usually have profoundly small realms of utilization. Combination 

homeopathy is easy to learn, as a minimal amount of training is needed 

for the doctor to perceive the symptomatic picture that is presented. 

In nature, everything exists in a combination form. Thus, Apis 

mellifica, or honey bee, is a very complex combination that nature has 

brought together to yield one energetic substance. This is the law of 

“synergy” – the sum of the whole is greater than that of the parts. 

“Combining” is the secret of life. 

This type of synergy is culminated in the Dr. Recommends’ combination 

remedies. The combination remedies have been developed with QQC TM 

techniques, to ensure that the blending of the ingredients have a 

synergistic effect and become a new singular formula. The Dr. 

Recommends’ combination remedies are safe and effective formulas that 

will minimize healing crises and help to reduce risk to the patient. The 

combination remedies also utilize the best of trace element work in 

achieving their glandular activity. 

83

COMBINATION REMEDIES 

ARRHYTH-1 (1 fl. oz.) 


Indication: Irregularities of the pulse 

Ingredients: Crataegus oxyacantha, Valeriana officinalis, Kali 

Phosphoricum, Amni visnaga, Leonurus Cardiac, Cytisus scoparius, 

Sumbul 2x. Heart, Nerium oleander 3x. Zincum Metallicum 5x. Iberis 

amara 6x. Sulphur, Platinum Metallicum 12x. 

ARTHRO 1 (1 fl. oz.) 


Indication: Joint stiffness and pain 

Ingredients: Angelica archangelica, Du Huo 2x. Magnesia Phosphorica 

2x, 3x, 6x. Dong Quai, Cnidium, Achyranthes, Gambir, Kali Muriaticum, 

Manganum Metallicum, Yucca filamentosa 3x. Cartilage 3x, 6x, 12x. 

Rhus toxicodendron 5x. Arsenicum Metallicum 6x. Hordeum vulgare 8x. 

Oxalicum Acidum 8x, 12x. Arnica montana 8x, 100x, 1000x. 

Antimonium, Borax, Baryta, Arsenicum Metallicum, Platinum 

Metallicum, Sulphur, Elastin, Elastase, Collagen, Collagenase 12x. 

CEPHALO-LD (1 fl. oz.) 


Indication: Learning disabilities, Mental clarity 

Ingredients: Convallaria majalis 2x, 6x. Cistus canadensis, Impatiens, 

Clematis erecta 6x, 12x, 30x, 60x, 100x, 500x, 1000x. Bovine Brain 

Tissue 6x, 12x. Sepia 8x. Phosphorus 10x. Zincum Metallicum, 

Belladonna 12x. Plumbum Metallicum, Platinum Metallicum 25x, 75x, 

100x. Mercurius Vivus 25x, 75x, 100x, 500x. Bovine Kidney Glandular, 

Lycopodium clavatum 30x. 

CEPHALO-M (1 fl. oz.) 


Indication: Stimulates blood flow to brain, Memory 

Ingredients: Euphrasia officinalis, Rosmarinus officinalis 2x. Salvia 

officinalis 2x, 6x. Artemisia vulgaris, Asparagus officinalis 3x. Ilex 

paraguariensis 5x. Convallaria majalis, Allium sativum, Calcarea 

Phosphorica 6x. Brain 6x, 12x, 30x, 60x, 100x. Baryta Carbonica 8x. 

Sulphur, Silicea, Selenium Metallicum, Zincum Metallicum 12x, 100x, 

1000x. Plumbum Metallicum 30x. 

84

CEPHALO-SD (1 fl. oz.) 


Indication: Memory, Brain power 

Ingredients: Gingko biloba, Choline, Phosphatydl Choline 2x. Taurine, 

Tyrosine 3x. Niacin, Niacinamide, Biotin 4x. Phenylalanine 5x. Nerve 

Growth Factor 6x. Brain Sarcode 6x, 12x, 30x, 60x, 100x. Vitamins: 

B1-B20 8x. Paullinia cupana 3x. 

COUGH SYRUP (4 fl. oz.) 


Indication: Cough 

Ingredients: Laurocerasus, Spongia tosta, Rumex crispus, Belladonna, 

Ipecacuanha, Drosera rotundifolia 3x. Mentha, Adrenalinum, Ligusticum 

porteri 4x. Convallaria majalis, Alumen, Bromium, Ferrum 

Phosphoricum, Zincum Metallicum, Manganum Metallicum, Magnesia 

Phosphorica, Baryta, Bismuthum Metallicum, Dextromethorphan 6x. 

Sarcodes: Cough Center, Lung 6x, 12x, 30x, 60x, 100x. Arsenicum 

Metallicum 8x. Stannum Metallicum 9x. Platinum Metallicum, Sulphur 

12x, 24x, 30x, 60x. 

CoQ (1 fl. oz.) 


Indication: Deficiencies of CoQ 

Ingredients: Sesame Seed oil, Avocado oil, Biotin, Folic acid, CoQ10 3x. 

CoA, CoQ6, CoQ7, CoQ9, Ascorbic palmitate 6x, 12x, 24x, 30x. 

DERMA-A (1 fl. oz.) 


Indication: Comedones, Pustules, Blackheads, Whiteheads 

Ingredients: Selenium Metallicum, Zincum Metallicum 4x. Cimicifuga 

racemosa 6x, 12x, 24x. Lymph 6x, 12x, 30x. Natrum Muriaticum 6x, 

200x. Argentum Metallicum, Aurum Metallicum, Gelsemium 

sempervirens, Iodium, Manganum Metallicum 8x. Placenta 9x. Kali 

Bromatum, Alumen, 12x, 24x, 60x. Juglans nigra 12x, 30x. Ledum 

palustre, Hepar Sulphuris Calcareum, Mercurius Vivus 30x, 60x, 100x. 

85

DERMA-I (1 fl. oz.) 


Indication: Itching 

Ingredients: Sarcodes: Liver, Lymph 3x, 6x, 12x, 30x, 60x, 100x. 

Selenium Metallicum, Zincum Metallicum, Borax, Magnesium 

Metallicum, Manganum Metallicum, Pangamicum Acidum 4x. Silicea, 

Graphites, Calcarea Carbonica 6x. Alumen, Arsenicum Metallicum, 

Baryta, Bismuthum Metallicum, Cuprum Metallicum, Stannum 

Metallicum, Nitricum Acidum 8x. Muriaticum Acidum, Sulphuricum 

Acidum 8x, 12x, 30x, 60x. Iodium, Phenylalanine, Tyrosine, 

Phenylpyruvic Acid 12x, 30x, 60x. Phenylalanine Hydroxylase, 

Glutamic-oxaloacetic Transaminase, Creatine Phosphokinase, Lactate 

Dehydrogenase 60x, 100x, 500x. 

EAR DROPS (1 fl. oz.) 


Indication: Ear ache and excess ear wax (external use) 

Ingredients: Olive Oil, Sesame Seed Oil. Verbascum thapsus 1x. 

Anthemis nobilis 2x. Plantago major 3x. Vanilla, Ferrum Phosphoricum 

4x, 6x. 

ENTERO-B (1 fl. oz.) 


Indication: Bowel flora disorders 

Ingredients: Large Intestine Sarcode, Colostrum 4x. Manganum 

Metallicum 6x. Natrum Muriaticum 6x, 100x, 1000x. Argentum 

Metallicum, Arsenicum Metallicum, Arum maculatum, Lactobacillus 12x. 

Bacteroidum 30x. 

ENTERO-C (1 fl. oz.) 


Indication: Constipation 

Ingredients: Senna, Cascara sagrada, Zincum Metallicum 3x. Borax, 

Ferrum Metallicum 6x. Alumina, Phosphorus 8x. Sulphur, Barium, 

Aurum Metallicum, Antimonium, Arsenicum Metallicum 12x. Iodium 

16x. Lycopodium clavatum 30x. 

EU-STRESS (1 fl. oz.) 


Indication: Stress 

Ingredients: Apis mellifica 2x, 6x. Royal Jelly 3x. Adrenalinum 3x, 6x, 

12x, 30x, 60x, 100x. Citrullus, Cistus canadensis, Impatiens, Clematis 

erecta, Zincum Metallicum, Ferrum Metallicum, Silicea 6x. 

Hypothalamus, Amygdala amara 6x, 12x, 30x, 60x, 100x. Vanadium 

Metallicum 8x, 12x, 30x. Lithium Carbonicum 12x, 30x, 60x. 

Neurotensin 16x, 30x, 60x, 100x. 

86

FEM-B (1 fl. oz.) 


Indication: Balance female organ systems 

Ingredients: Caulophyllum thalictroides 2x, 6x. Rubus idaeus, 

Cimicifuga racemosa 6x. Sarcodes: Ovary, Corpus Luteum, Uterus, 

Mammary, Hypothalamus, Pituitary, Adrenal, Estrogen, Progesterone 6x, 

12x, 30x, 100x, 500x, 1000x. Mercurius Vivus, Petroleum, Baryta, 

Sulphur 20x. 

FEM-M (1 fl. oz.) 


Indication: Menopausal conditions 

Ingredients: Chamomilla 3x, 30x, 100x, 500x, 1000x. Cimicifuga 

racemosa, Sanguinaria canadensis, Ovarian Sarcode 6x. Silicea 8x. 

Borax, Graphites, Iodium, Phosphorus, Estrogen 12x. Lachesis mutus 

16x. 

FEM-PMS (1 fl. oz.) 


Indication: Premenstrual cramping, Irritability and depression 

Ingredients: Chamomilla, Vitamin B6 3x. Caulophyllum thalictroides 3x, 

6x. Cimicifuga racemosa 4x. Magnesia Phosphorica, Magnesia 

Carbonica, Natrum Muriaticum 6x. Manganum Metallicum 6x, 12x, 30x. 

Estrogen, Progesterone 6x, 12x. Natrum Carbonicum 12x. Phosphorus 

30x. Platinum Metallicum 30x, 100x. 

GASTRO-I (1 fl. oz.) 


Indication: Stomach lining ulcerations 

Ingredients: Oryza sativa, Panicum miliaceum, Triticum repens, Poria, 

Raphanus sativus, Brassica, Zingiber officinale, Glycyrrhiza glabra, 

Disodium Phosphate 2x. Borax 6x. Sarcodes: Stomach, Small Intestine 

6x, 12x, 30x, 60x, 100x. Calcarea Carbonica 8x. Carbo Vegetabilis 8x, 

12x, 30x. Mercurius Vivus, Arsenicum Metallicum 30x. Plumbum 

Metallicum 100x. Sulphur, Cuprum Metallicum, Selenium Metallicum 

200x. 

GLUCO-H (1 fl. oz.) 


Indications: Hypoglycemia 

Ingredients: Oenothera biennis 3x. Chromium Metallicum 6x. ATP, 

Insulin, Pancreas 6x, 12x, 30x. Plumbum Metallicum, Antimonium 

Metallicum, Arsenicum Metallicum 20x. Nux vomica 30x. Saccharum 

Officinale 30x, 200x, 1000x. 

87

GLUCO-I (1 fl. oz.) 


Indication: Hereditary tendency toward diabetes 

Ingredients: Lycopodium clavatum, Selenium Metallicum, Zincum 

Metallicum, Sulphur, Chromium, Alumen 6x. Sarcodes: Hypothalamus, 

Posterior Pituitary, Kidney, Pancreas 6x, 12x, 30x, 60x, 100x. Argentum 

Metallicum, Bismuthum Metallicum, Barium 12x. DNA, Insulin 12x, 

60x, 100x, 1000x. Gelsemium sempervirens, Iodium, Plumbum 

Metallicum 20x. Uranium, Phosphoricum Acidum 30x. Radium 

Bromatum, ATPase, Antidiuretic Hormone 60x. Glucose, Glycogen 

1000x. 

HEMO-L (1 fl. oz.) 


Indication: White blood cell disorders 

Ingredients: Ceanothus americanus 2x. Nux vomica, Thuja occidentalis 

3x. Ipecacuanha 4x, 6x, 12x. Leukemia Nosode 6x, 8x, 12x, 30x, 60x, 

100x, 1000x. Hapalochlaena maculata, Sarcodes: Lymph, Spleen 6x, 

12x, 30x, 60x, 100x. Leukocytes 12x, 30x, 60x, 100x. Phosphorus, 

Natrum Muriaticum 30x, 60x, 100x. 

HYPERTHYRO 1 (1 fl. oz.) 


Indication: Iodine sensitivity, Over-active thyroid 

Ingredients: Selenium Metallicum, Vitamin A 2x. Bovine Pituitary 

Glandular 6x. Thyroidinum 12x, 24x, 30x. Sulphur, Arsenicum 

Metallicum 16x. Mercurius Vivus, Molybdenum 20x. Iodium, Natrum 

Muriaticum 30x. TSH 30x. 

HYPERTONIA 2 (4 fl. oz.) 


Indication: High blood pressure 

Ingredients: Valeriana officinalis 2x. Citricum Acidum, Kali Bitartrate 

3x. Rauwolfia serpentina, Fucus vesiculosus 4x. Kali Muriaticum, Kali 

Phosphoricum 4x, 5x, 6x, 12x. Rhamnus purshiana, Allium sativum, 

Rennin, Sarcodes: Mid Brain, Kidney, Liver, Collective Arterial 6x. 

Vasopressin, Angiotensin I, II, Neurotensin 8x, 12x, 30x, 60x, 100x, 

500x. 

HYPOTONIA 1 (1 fl. oz.) 


Indication: Low blood pressure 

Ingredients: Crataegus oxyacantha 2x. Nerium oleander, Laurocerasus, 

Cytisus scoparius 3x. Zincum Metallicum, Natrum Sulphuricum 6x. 

Chromium 8x. Angiotensin 12x. 

88

IMMUNOPOIE (1 fl. oz.) 


Indication: Stimulates immune system 

Ingredients: Petroselinum sativum, Natrum Muriaticum 3x. Bovine 

Glandulars: Thymus, Bone Marrow, Liver, Spleen, Adenoids, Tonsils 5x, 

6x, 12x, 30x, 100x. Aurum Metallicum, Argentum Metallicum, Sulphur 

12x. Appendix 15x, 30x, 100x. Mercury Amalgam 100x, 500x, 1000x. 

Saccharinum 100x 

INFLU-F (1 fl. oz.) 


Indication: Flu and fever like symptoms 

Ingredients: Euphrasia officinalis, Ulmus fulva 2x. Pulsatilla 2x, 6x, 

12x. Dulcamara 3x. Ferrum Phosphoricum, Ruta Graveolens 4x. 

Zincum Metallicum, Bismuthum Metallicum, Adrenalinum, Thuja 

occidentalis, Hyssopus officinalis 6x. Aconitum napellus 6x, 8x, 12x. 

Belladonna 8x. Rhus toxicodendron, Camphora, Manganum Metallicum, 

Phosphorus, Iodium 12x. 

INFLU-I (1 fl. oz.) 


Indication: Intestinal flu symptoms 

Ingredients: Chamomilla, Marrubium vulgare 1x. Mentha piperita, 

Lavandula officinalis, Ocimum basilicum, Citrus limonum, Populus 

candicans 2x. Pogostemon patchouli 3x. Zincum Metallicum, 

Symphytum officinale 6x. Sulphur, Argentum Metallicum, Iodium, 

Manganum Metallicum, Alumen, Phosphorus 12x. 

ME 1 (1 fl. oz.) 


Indication: Epstein Barr related conditions 

Ingredients: Zincum Metallicum, Natrum Muriaticum, Natrum 

Phosphoricum, Natrum Sulphuricum, Natrum Carbonicum 6x. 

Antimonium, Lithium 12x. Epstein Barr Virus, Mononucleosis, 

Hemolytic Influenza, Hemolytic Streptococcus, CMV 16x, 24x, 30x, 100x. 

METABOLIC 1 (1 fl. oz.) 


Indication: Metabolic disorders 

Ingredients: All Glandulars 5x-30x, 60x-100x, 500x, 1000x. All Cell 

Salts 6x-12x, 30x-500x, 1000x. All Amino Acids 10x-30x, 50m. All Parts 

of Krebs Cycle 12x-30x, 50m. RNA/DNA 30x-100x, 50m. Chromosomes 

12x, 30x, 60x, 100x, 500x, 1000x. Collective Miasms: Psorinum, 

Sycosis, Syphilinum 500x, 1000x, 2000x, 50m. 

89

MUCOUSLYSIS (4 fl. oz.) 


Indication: Mucous conditions 

Ingredients: Plantago major, Urtica dioica, Equisetum arvense 1x. 

Eucalyptus globulus 2x. Lobelia cardinalis, Vinca minor, Ephedra 

vulgaris 3x. Calcarea Iodata 5x. Sarcodes: Lymph, Pancreas 6x, 12x, 

30x, 60x, 100x. Arsenicum Iodatum 8x. Mucin 30x, 60x, 100x. 

mRNA (4 fl. oz.) 


Indication: Resets mesenger RNA for intercellular regulation 

Ingredients: Mercaptoethanol 12x, 30x, 60x, 100x, 500x, 1000x. mRNA 

100x, 500x, 1000x. 

NASO-I (1 fl. oz.) 


Indication: Rhinitis, Sinusitis 

Ingredients: Natrum Muriaticum, Manganum Metallicum, Zincum 

Metallicum 4x, 6x, 12x. Allium cepa, Allium sativum 6x. All Sinuses 6x, 

12x, 30x, 60x, 100x. Pulsatilla 12x. Sulphur, Aluminium Metallicum, 

Mercurius Vivus, Stannum Metallicum, Bromium, Borax 30x, 100x. 

NEO-P (1 fl. oz.) 


Indication: Degenerative tissue 

Ingredients: Naja tripudians 5x, 12x, 30x. Zincum Metallicum, Calcarea 

Phosphorica, Sulphur, Antimonium 6x, 12x, 30x, 60x, 100x. Bovine 

Glandulars 6x, 16x. Viscum album 6x, 12x, 100x. Cuprum Metallicum, 

Arsenicum Metallicum 8x, 12x, 30x. Interferon: Alpha, Beta, Gamma, 

Interleuken: I, II, III 12x, 24x, 30x. Taxus baccata 12x-30x. Carcinum 

12x, 30x, 100x, 500x, 1000x. 

NEURO-R (4 fl. oz.) 


Indication: Stress and nerval over-stimulation 

Ingredients: Panax quinquefolium, Zincum Valerianicum, Lecithin 3x, 

12x, 30x. Serotonin 5x. Cistus canadensis, Impatiens, Clematis erecta 

6x. Pulsatilla, Magnesia Phosphorica, Passiflora incarnata, Valeriana 

officinalis, Coffea cruda, Lithium Carbonicum, GABA 6x, 12x. 

Acetylcholine 6x, 12x, 30x, 60x, 100x. Aconitum napellus, Selenium 

Metallicum 8x. Arsenicum Iodatum, Endorphins, Neurotensin 12x, 30x, 

60x. Gelsemium sempervirens 18x, 24x, 30x. Cuprum Metallicum, 

Aluminium Metallicum 30x, 100x. 

90

PROSTA-I (1 fl. oz.) 


Indication: Inflamed prostate 

Ingredients: Bee Pollen, Zincum Metallicum 3x. Prostate 6x, 12x, 30x, 

60x, 100x, 500x, 1000x. Capsicum annuum 6x, 12x. Natrum 

Sulphuricum 6x, 12x, 30x. Baryta Carbonica, Pulsatilla 12x. Plumbum 

Metallicum, Platinum Metallicum, Cadmium Metallicum 12x, 30x, 60x, 

100x, 500x. Tuberculinum, Thuja occidentalis 16x, 30x, 100x, 1000x. 

PULMO-A (1 fl. oz.) 


Indication: Asthmatic-like conditions 

Ingredients: Arsenicum Album 4x, 6x, 8x. Bryonia 2x, 6x, 12x. 

Adrenalinum 3x, 6x. Zincum Metallicum, Silicea, Carbo Vegetabilis 6x. 

Lung Sarcode 6x, 12x, 30x, 60x, 100x. Lithium Carbonicum 8x. 

Camphora 12x, 30x. Histamine 16x, 24x, 30x. Belladonna, Natrum 

Muriaticum 30x. NADP, NAD, NADH 60x, 100x, 500x. Natrum 

Sulphuricum 200x. 

PULMO-P (1 fl. oz.) 


Indication: Pulmonary infections and accompanying pain 

Ingredients: Asclepias tuberosa 3x. Bovine Lung Tissue, Sepia, 

Cinchona officinalis 6x. Silicea 6x, 12x, 30x. Picricum Acidum 8x. 

Arsenicum Iodatum, Bryonia 12x. Sulphur 12x, 30x. Selenium 

Metallicum 12x, 30x, 100x. Cuprum Metallicum, Stannum Metallicum, 

Aurum Metallicum, Platinum Metallicum 18x, 30x. Calcarea Carbonica, 

Lycopodium clavatum, Phosphorus 30x. Mercurius Vivus 100x, 500x. 

PURATIVE (1 fl. oz.) 


Indication: Cleans microorganism infestations from the body 

Ingredients: Hydrastis canadensis 1x. Citrus paradisi semen 2x. Aloe 

socotrina, Benzoin 3x. Chrysanthemum coccineum, Vitamins: A, C, E 

4x. 

REN-P (1 fl. oz.) 


Indication: Excess urinary protein, Enzymatic disturbance 

Ingredients: Kidney 6x, 12x. Vita Mar 8x. Phosphorus, Ledum palustre 

12x. Albumin, Petroleum 12x, 30x. Mercurius Vivus 20x, 30x, 100x. 

Silicea, Sulphur, Zincum Metallicum 30x. 

91

RENLAPIS (1 fl. oz.) 


Indication: Kidney pain, Gravel urine 

Ingredients: Crataegus oxyacantha 2x, 6x. Sarsaparilla 3x. Digitalis 

purpurea 3x, 6x. Nitricum Acidum, Berberis vulgaris, Lycopodium 

clavatum 6x. Kidney Sarcode 6x, 12x, 30x, 60x, 100x. Bismuthum 

Metallicum, Borax 8x. Stannum Metallicum 10x. Lithium, Selenium 

Metallicum 12x. Oxalicum Acidum, Uricum Acidum 30x. 

SARCOESIS (1 fl. oz.) 


Indication: Inflammatory and swelling conditions 

Ingredients: Chrysanthemum parthenium 2x. Zincum Metallicum, 

Verbascum thapsus 3x. Urtica dioica 4x. Apis mellifica 4x, 6x, 12x, 

30x. Adrenalinum 4x, 6x, 12x, 30x, 60x, 100x. Belladonna 5x, 6x, 12x, 

30x. Crotalus horridus 6x. Silicea, Triosteum perfoliatum 6x, 12x. 

Natrum Muriaticum, Magnesia Phosphorica, Kali Sulphuricum, Lymph 

6x, 12x, 30x, 60x, 100x. Hepar Sulphuris Calcareum 8x, 16x, 30x. 

Lachesis mutus 12x, 30x. Chymotrypsin, Histidine, Histamine, ATPase 

Lysozyme, 12x, 30x, 60x, 100x. Glucose-6-Phosphatase, Coenzyme A 

Dehydrogenase 30x, 60x, 100x. Biopterin, Hepar Suis 100x, 500x, 

1000x 

SHARK CARTILAGE (1 fl. oz.) 


Contains the nutritional factors of shark cartilage 

Ingredients: Shark Cartilage 3x, 6x, 12x, 30x. Thymol, Sarcode: 

Thymus 4x, 6x, 12x. Sarcode: Lymph 5x, 15x, 30x. Natrum 

Muriaticum, Mentha piperita 6x. Silicea 12x, 30x, 60x. 

THERACEPHALIC (1 fl. oz.) 


Indication: Brain circulation after stroke or injury 

Ingredients: Scutellaria lateriflora 3x. Convallaria majalis 3x, 6x, 12x. 

Taurine, Tyrosine 3x, 12x, 60x. Thyroidinum 5x. Magnesia 

Phosphorica, Manganum Metallicum 6x, 12x, 30x, 60x, 100x. 

Variolinum 12x, 30x, 60x, 100x. Stannum Metallicum 8x. Sarcodes: 

Brain, Arterial Wall 12x, 30x, 60x, 100x. 

92

THERACIRCULO (1 fl. oz.) 


Indication: Circulatory disorders 

Ingredients: Niacinum, Niacinamidum 2x. Adrenalinum, Camphora 4x. 

Aorta Valve, Ferrum Metallicum 6x, 12x, 30x. Thrombin, Proteolytic 

Enzymes 8x, 24x, 30x, 100x. Stannum Metallicum 8x, 24x, 50x. 

Sulphur, Heloderma, Aesculus hippocastanum, Crotalus horridus 12x. 

Tabacum 12x, 24x. Arterial Tissue 12x, 30x. Baryta 20x. Arnica 

montana 100x. 

TRAUMATIC 1 (1 fl. oz.) 


Indication: Injuries, Rebuilds cellular tissue 

Ingredients: Echinacea purpurea 3x. Arnica montana 3x, 6x, 12x, 100x, 

1000x, 50lm. Sulphur 3x, 12x. Calendula officinalis 3x, 12x, 30x, 100x, 

1000x, 50lm. Symphytum officinale 5x, 12x, 30x, 60x, 100x. Bone 

Marrow 6x, 12x, 30x, 60x, 100x, 500x. Niccolum Metallicum 10x, 30x, 

100x. Rhus toxicodendron, Barium, Bromium, Bismuthum Metallicum 

12x, 30x, 60x, 100x. Arsenicum Metallicum 100x. 

VENA-H (1 fl. oz.) 


Indication: Hemorrhoidal conditions 

Ingredients: Aesculus hippocastanum 2x. Collinsonia canadensis 3x. 

Nux vomica 4x. Lycopodium clavatum, Sulphur 5x. Cuprum 

Metallicum, Nitricum Acidum, Graphites, Veins 6x. Liver Aliesterase, 

Proteolytic Enzyme, Chymotrypsin, Vanadium Metallicum 8x. 

VIR-H (1 fl. oz.) 


Indication: Herpes, Cold sores 

Ingredients: Silicea 5x. Selenium Metallicum, Euphrasia officinalis, 

Trifolium pratense 6x. Sulphur, Antimonium Crudum, Arsenicum 

Metallicum, Iodium 12x. Plumbum Metallicum 16x. Herpes simplex I, 

II, III, Herpes zoster, Herpes progenitalis 16x, 24x, 30x, 100x. Thuja 

occidentalis 30x. 

93

THE RESTORATIVE PHILOSOPHY 

Sarcode remedies have been used for many years in homeopathy to 

help rebuild and correct tissues when organ structures are in disease 

states. Damage caused by disease states in organs can result in 

malfunctioning on an organic level. The Dr. Recommends’ restorative 

remedies help the tissues to rebuild. Energetic students have shown 

that a potent glandular can rectify an energetic imbalance where there 

is no organic disturbance. This is covered in The Experimental Data on 

Homeopathy by Dr. William Nelson, and shows the uses and proposed 

mechanisms of sarcodal homeopathy. 

Sarcodal homeopathy offers the safest and most gentle form of 

homeopathy. Results are often the slowest to be seen due to the 

correct rebuilding of the degenerative cells in the organs. The 

restorative remedies will work more quickly and successfully in 

younger patients than in older ones. In the older patient, these 

remedies can at times be utilized to stimulate cleansing and to 

stabilize and reduce the risk of a healing crisis. 

The Dr. Recommends’ restorative homeopathics are engineered in 

homochords of differing potencies. Maximum efficiency is achieved 

with a combination of 4x, 6x, 12x, 30x, 60x, 100x, 500x, and 1000x. 

This allows the body to respond to the frequency of dilution which 

works best to rebuild tissues. The restorative remedies are safe and 

effective and quality controlled by the QQC TM techniques to ensure 

efficacy. 

94

RESTORATIVE REMEDIES 

Ingredients: New Zealand or American Ursa and Bovine Glandulars 

4x, 6x, 12x, 30x, 60x, 100x, 500x, and 1000x. 

Bone and Bone Marrow 

Brain 

Cervical 

Cranial, Sacral 

Ear 

Eye 

Gallbladder 

Heart, Lung 

Kidney, Ovarian, Adrenal 

Kidney, Prostate, Adrenal 

Liver, Gallbladder 

Lymph, Spleen, Mammary 

Major Nerves 

Muscle, Ligament, Cartilage 

Orchic 

Pancreas, Stomach 

Pineal, Pituitary, Hypothalamus 

Sinuses 

Skin and Mucous Membrane 

Small and Large Intestine 

Thoracic 

Thyroid, Thymus, Parathyroid 

95

SARCODES 

Sarcodal homeopathy involves using healthy glandular tissue from a 

healthy organism to treat sick conditions within the body. For an 

expanded view of sarcodes and the experimental context behind them 

read The Experimental Data on Homeopathy, by Dr. William Nelson. In 

the text it outlines exactly how sarcodal homeopathy works. Sarcodal 

homeopathy promotes growth and development of healthy glandular 

tissue. 

Within this treatise, many different sarcodes will be classified that can 

be used by a knowledgeable homeopath. The list of sarcodal tissues used 

here is very large and may be beyond the grasp of some homeopaths. We 

have a variety of tissues being used by homeopaths in many ways. Since 

these sarcodal tissues help to rebuild tissue, help tissue to organize 

properly, and increase the probability of the presence of healthy tissue 

over old tissue, it is possible to see how homeopathy can be used. 

Sarcodal tissue can go beyond mere tissue to secretions; which include 

hormones, enzymes, coenzymes, RNA, DNA, and others. Thus, we can 

see from the long list a wide range of sarcodal tissues that can be 

brought beyond just tissue to include secretions of the body. This vast 

array of secretions is broadened to include as many different hormones 

and enzymes known by Dr. Nelson at this time. 

96

SARCODES I 

ADENOIDS 

ADRENAL 

ADRENAL GLANDULAR 

APPENDIX 

AUDITORY NERVE 

BONE MARROW 

BOWEL FLORA 

BRAIN 

CEREBRUM 

CORPUS CALLOSUM 

CORPUS LEUTEUM 

CYSTERNA CHYLI 

EMOTIONS 

ESONOPHIL 

FRONTAL LOBE 

GALLBLADDER 

HEART 

HYPOTHALAMUS 

ILEO CECAL VALVE 

INTRINSIC FACTOR 

ISLE OF LANGERHANS 

KIDNEY 

LARGE INTESTINE 

LIMBIC SYSTEM 

LIVER 

LEUCOCYTE 

LUNG 

LYMPHOCYTE 

MAMMARY GLANDS 

MEDULA 

MICHELLE BALANCE 

MID BRAIN 

MONOCYTE 

MOUTH 

NERVES OF ABDOMEN (PERIPHERAL SPINAL NERVES) 

OCCIPITAL 

OCULOMOTOR 3 (CRANIAL NERVES) 

OLFACTORY HAIRS (CILIA) (SMELL) 

OLFACTORY MUCOSA (SMELL) 

OLFACTORY NEURONS (SMELL) 

OLFACTORY PLATE (SMELL) 

OLFACTORY TRACT (SMELL) 

OLFACTORY 1 (CRANIAL NERVES) 

97

SARCODES I, cont. 

OPTIC CHIASMA (RELATED STRUCTURES-BRAIN STEM) 

OPTIC DISC (LAYERS OF THE EYE: RETINA-EYE) 

OPTIC NERVE (EYE) 

OPTIC 2 (CRANIAL NERVES) 

ORGAN OF CORTI (INTERNAL EAR-EAR) 

OTIC (GANGLIA-PARASYMP) 

OTOLOTHS (EQUILIBRIUM: MACULA-EAR) 

OVAL WINDOW (INTERNAL EAR-EAR) 

OVARIES 

PAIN (SENSORY) 

PANCREAS 

PARATHYROID 

PARIETAL LOBE 

PELVIC/PERINEAL VISCERA (POSTGANGLIONIC NEURONS-AUTOSYMP) 

PERINEURIUM (MOTOR NERVES) 

PERSONALITY (BRAIN) 

PINEAL 

PITUIPOSTERIOR 

PITUITANTERIOR 

PITUITARY 

POLYMORPH 

PONS (HINDBRAIN-BRAIN STEM) 

PONS (MOTOR NERVES) 

PONTINE CISTERN (SUBARACHNOID SPACES-CERE FLUID) 

PORE CANAL (TASTE BUDS-TASTE) 

POST GANGLIONIC AXONS (AUTOSYMP) 

POST GANGLIONIC CELL BODIES (AUTOSYMP) 

POSTERIOR FUNICULUS (SPINAL CORD-WHITE MATTER) 

POSTERIOR HORNS (SPINAL CORD-GRAY MATTER) 

POSTERIOR MEDIAN SULCUS (SPINAL CORD) 

POSTERIOR RAMUS (MOTOR NERVES) 

PRECENTRAL GYRUS (MOTOR NERVES) 

PREGANGLIONIC AXONS (AUTOSYMP) 

PREGANGLIONIC CELL BODIES (AUTOSYMP) 

PREVERTEBRAL GANGLIA (AUTOSYMP) 

PREVERTEBRAL GANGLIA (POSTGANGLIONIC NEURONS-AUTOSYMP) 

PRINCIPAL SPEECH AREA (FRONTAL LOBE-CEREBRUM) 

PROSTAGLANDIN 

PTERYGOPALATINE (GANGLIA–PARASYMP) 

PUPIL (EYE) 

PYRAMIDS (MYELENCEPHALON-BRAIN STEM) 

RECEPTOR CELLS (TASTE BUDS-TASTE) 

RECKLESS (EMOTION) 

RETICULAR FORMATION 

98


RETINAL ARTERIES (LAYERS OF THE EYE: RETINA-EYE) 

RHINENCEPHALIN 

SACCULE/UTRICLE (INTERNAL EAR-EAR) 

SEMICIRCULAR CANALS (INTERNAL EAR-EAR) 

SEMICIRCULAR DUCTS (INTERNAL EAR-EAR) 

SENSORY AREA (PARIETAL LOBE-CEREBRUM) 

SKELETAL MUSCLES (MOTOR NERVES) 

SKIN (MOTOR NERVES) 

SMALL INTESTINE 

SPINAL CORD (RELATED STRUCTURES-BRAIN STEM) 

SPINAL NERVES (MOTOR NERVES) 

SPINAL NERVES (POSTGANGLIONIC NEURONS-AUTOSYMP) 

SPLANCHNIC NERVE (AUTOSYMP) 

SPLANCHNIC NERVE (PREGANGLIONIC NEURONS-AUTOSYMP) 

SPLEEN 

STALK OF HYPOPHYSIS (RELATED STRUCTURES-BRAIN STEM) 

STAPES (MIDDLE EAR-EAR) 

STOMACH 

STOMACH ACID 

SUBARACHNOID SPACE (ARACHNOID-MENINGES) 

SUBMANDIBULAR (GANGLIA-PARASYMP) 

SUPERFICIAL FASCIA (MOTOR NERVES) 

SUPERIOR CEREBELLAR PEDUNCLE (MIDBRAIN-BRAIN STEM) 

SUPERIOR CISTERN (SUBARACHNOID SPACES-CERE FLUID) 

SUPERIOR COLLICULI (MIDBRAIN-BRAIN STEM) 

SUPPORTING CELLS (EQUILIBRIUM: CRISTA-EAR) 

SUPPORTING CELLS (INTERNAL EAR-EAR) 

SUPPORTING CELLS (SMELL) 

SUPPORTING CELLS (TASTE BUDS-TASTE) 

SUSPENSORY LIGAMENT (EYE) 

SWEAT GLANDS (TO SKIN – AUTOSYMP) 

SYMPATHETIC CHAIN (POSTGANGLIONIC NEURONS-AUTOSYMP) 

SYMPATHETIC CHAIN OF GANGLIA (AUTOSYMP) 

TECTORIAL MEMBRANE (INTERNAL EAR-EAR) 

TEMPORAL LOBE 

TEMPORAL MANDIBULAR JOINT 

TENTORIUM CEREBELLI (DURA MATTER-MENINGES) 

TESTIS 

THALAMUS (DIENCEPHALON) 

THIRD VENTRICULE (DIENCEPHALON) 

THORACIC DUCT 

THORACIC VISCERA (POSTGANGLIONIC NERUONS-AUTOSYMP) 

THYMUS 

THYROID 

99


TMJ 

TONSILS 

TOUCH-PRESSURE (SENSORY) 

TRIGEMINAL (PERIPHERAL SPINAL NERVES) 

UTERUS 

VAGUS NERVE 

VALVE OF HOUSTON 

WBC 

100

SARCODES II 

1 ST – 12 TH CRANIAL NERVES 

FRONTAL BONE 

INFA CONCHA VERTEBRAE 

INTESTINE, SMALL/LARGE 

LYMPH, SPLEEN, MAMMARY 

MAXILLAE 

M1 

3 RD – 6 TH NERVE 

OCCIPITAL 

OCCIPITAL CONDYLES 

OCCIPUT 

OLFACTORY NERVE 

OPTICAL NERVE 

PALATINE BONE 

PARIETAL BONE 

SACROILIAC 

SACRUM 

SPHENOID 

SQUAMA 

STOMACH, PANCREAS 

TEAR DUCTS 

TEMPORAL BONE 

TRIGEMINAL 5 (CRANIAL NERVES) 

TROUCHLEAT 4 (CRANIAL NERVES) 

TYMPANIC MEMBRANE (EXTERNAL EAR-EAR) 

VAGUS NERVE 

VENTRAL ROOT (MOTOR NERVES) 

VENTRAL (ANTERIOR) ROOT (SPINAL CORD-SPINAL NERVES) 

C1-C7 VERTEBRAE 

L1-L5 VERTEBRAE 

T1-T12 VERTEBRAE 

VESTIBULAR PATHWAY (PERIPHERAL SPINAL NERVES) 

VESTIBULE (INTERNAL EAR-EAR) 

VESTIBULOCOCHLEAR 8 (CRANIAL NERVES) 

VISCERAL AFFERENT PATHWAY (PERIPHERAL SPINAL NERVES) 

VISUAL AREA (OCCIPITAL LOBE-CEREBRUM) 

VITREOUS BODY (LAYERS OF THE EYE: SPACES/FLUID-EYE) 

VOMER BONE 

WHITE COMMISSURES (SPINAL CORD-WHITE MATTER) 

WHITE RAMUS COMMUNICANS (AUTOSYMP) 

ZYGOMA BONE 

101

SARCODES III 

ABDOMINAL VISCERA (POSTGANGLIONIC NEURONS-AUTOSYMP) 

ABDUCENS 6 (CRANIAL NERVES) 

ACCESSORY 11 (CRANIAL NERVES) 

AGGRESSION 

AMYGDALA (DIENCEPHALON) 

ANGER (EMOTION) 

ANTERIOR CORTICOSPINAL TRACT (MOTOR NERVES) 

ANTERIOR CUTANEOUS DIVISION (MOTOR NERVES) 

ANTERIOR FUNICULUS (SPINAL CORD-WHITE MATTER) 

ANTERIOR HORNS (SPINAL CORD-GRAY MATTER) 

ANTERIOR MEDIAN FISSURE (SPINAL CORD) 

ANTERIOR RAMUS (MOTOR NERVES) 

ANXIETY (EMOTION) 

ARRECTOR PILI (TO SKIN-AUTOSYMP) 

ASSOCIATION NEURON (MOTOR NERVES) 

ASSOCIATION TRACTS (SUBDIVISIONS OF WHITE MATTER-CEREBRUM) 

AUDITORY AREA (TEMPORAL LOBE-CEREBRUM) 

AUDITORY (EUSTACHIAN) VERSTIBULE (MIDDLE EAR-EAR) 

AURICLE (EXTERNAL EAR-EAR) 

AUTISTIC (EMOTION) 

AXONS (MOTOR NERVES) 

AXONS (PREGANGLIONIC NEURONS-AUTOSYMP) 

AXONS – EYE, NASAL, ORAL, ETC. (POSTGANGLIONIC AXONS-PARASYMP) 

AXONS – HEAD & NECK (POSTGANGLIONIC NEURONS-AUTOSYMP) 

AXONS – S2, S3, & S4 (PREGANGLIONIC NEURONS-PARASYMP) 

AXONS – 3, 7, 9, 10 CRANIAL NERVES (PREGANG. NEURONS- 

PARASYMP) 

BASILAR MEMBRANE (INTERNAL EAR-EAR) 

BLOOD VESSELS (TO SKIN-AUTOSYMP) 

BONY LABYRINTH (INTERNAL EAR-EAR) 

CARELESS (EMOTION) 

CAUDATE NUCLEUS (BASAL NUCLEI-CEREBRUM) 

CAUDATE NUCLEUS (DIENCEPHALON) 

CELL BODIES (POSTGANGLIONIC AXONS – PARASYMP) 

CELL BODIES (POSTGANGLIONIC NEURONS- AUTOSYMP) 

CELL BODIES (PREGANGLIONIC NEURONS – AUTOSYMP) 

CELL BODIES (PREGANGLIONIC NEURONS – PARASYMP) 

CENTRAL CANAL 

CENTRAL CANAL (VENTRICLES-CERE FLUID) 

CENTRAL SULCUS (MAJOR FISSURES-CEREBRUM) 

CEREBELLUM (HINDBRAIN-BRAIN STEM) 

CEREBRAL AQUEDUCT (MIDBRAIN-BRAIN STEM) 

CEREBRAL AQUEDUCT (VENTRICLES-CERE FLUID) 

CEREBRAL PEDUNCLE (MIDBRAIN-BRAIN STEM) 

102

SARCODES III, cont. 

CEREBRAL PEDUNCLE (MOTOR NERVES) 

CHOROID PLEXUS (CERE FLUID) 

CILIARY (GANGLIA-PARASYMP) 

CILIARY BODY 

CILIARY PROCESSES (LAYERS OF THE EYE: CHOROID-EYE) 

CIRCUMVALLATE (PAPILLAE-TASTE) 

COCHLEA (INTERNAL EAR-EAR) 

COCHLEAR (PERIPHERAL SPINAL NERVES) 

COCHLEAR DUCT (INTERNAL EAR-EAR) 

COGNITION (BRAIN) 

COMMISSURE (SUBDIVISIONS OF WHITE MATTER-CEREBRUM) 

CONFUSION (EMOTION) 

CONJUNCTIVA (EYE) 

CORNEA (LAYERS OF THE EYE: SCLERA-EYE) 

CORONA RADIATA (MOTOR NERVES) 

CORONA RADIATA (PROJECTION TRACTS-CEREBRUM) 

CORPUS CALLOSUM (DIENCEPHALON) 

CUPOLA (EQUILIBRIUM: CRISTA-EAR) 

CUTANEOUS DIVISION (MOTOR NERVES) 

CRIBRIFORM PLATE (SMELL) 

DELUSION (EMOTION) 

DEPRESSION (EMOTION) 

DORSAL ROOT (MOTOR NERVES) 

DORSAL (POSTERIOR) ROOT (SPINAL CORD-SPINAL NERVES) 

DORSAL ROOT GANGLION (SPINAL CORD-SPINAL NERVES) 

EFFECTOR (MOTOR NERVES) 

EMR (SENSORY) 

ENDOLYMPHATIC DUCT (INTERNAL EAR-EAR) 

ENDONEURIUM (MOTOR NERVES) 

EPINEURIUM (MOTOR NERVES) 

EPITHALAMUS (DIENCEPHALON) 

EXTERNAL AUDITORY MEATUS (EXTERNAL EAR-EAR) 

FACIAL 7 (CRANIAL NERVES) 

FACILATATING EFFECT (MOTOR NERVES) 

FALX CEREBRI (DURA MATER-MENINGES) 

FEAR (EMOTION) 

FILIFORM (PAPILLAE-TASTE) 

FILUM TERMINALE (PIA MATTER-MENINGES) 

FOURTH VENTRICLE (HINDBRAIN-BRAIN STEM) 

FOURTH VENTRICLE (MYELENCEPHALON-BRAIN STEM) 

FOVEA CENTRALIS (LAYERS OF THE EYE: RETINA-EYE) 

FUNGIFORM (PAPILLAE-TASTE) 

GLOSSOPHARYNGEAL 9 (CRANIAL NERVES) 

GRAY COMMISSURES (SPINAL CORD-GRAY MATTER) 

103


GRAY RAMUS COMMUNICANS (AUTOSYMP) 

GREAT CISTERN (SUBARACHNOID SPACES-CERE FLUID) 

HAIR CELLS (EQUILIBRIUM: CRISTA-EAR) 

HAIR CELLS (EQUILIBRIUM: MACULA-EAR) 

HAIR CELLS (INTERNAL EAR-EAR) 

HAPTIC (SENSORY) 

HEAT-COLD (SENSORY) 

HYPOGLOSSAL 12 (CRANIAL NERVES) 

HYPOPHYSIS (DIENCEPHALON) 

HYPOTHALAMUS (DIENCEPHALON) 

INCUS 

INFERIOR COLLICULI (MIDBRAIN-BRAIN STEM) 

INHIBITING EFFECT (MOTOR NERVES) 

INTERMEDIATE ZONE (SPINAL CORD-GRAY MATTER) 

INTERNAL CAPSULE (DIENCEPHALON) 

INTERNAL CAPSULE (MOTOR NERVES) 

INTERNAL CAPSULE (PROJECTION TRACTS-CEREBRUM) 

INTERPENDUNCULAR CISTERN (SUBARACHNOID SPACES-CERE 

FLUID) 

INTERVENTRICULAR FORAMEN (VENTRICLES-CERE FLUID) 

INTRAMURAL (GANGLIA-PARASYMP) 

JOY (EMOTION) 

LATERAL CORTICOSPINAL TRACT (MOTOR NERVES) 

LATERAL CUTANEOUS DIVISION (MOTOR NERVES) 

LATERAL FISSURE (MAJOR FISSURES-CEREBRUM) 

LATERAL FUNICULUS (SPINAL CORD-WHITE MATTER) 

LATERAL HORNS (SPINAL CORD-GRAY MATTER) 

LATERAL RETICULOSPINAL (MOTOR NERVES) 

LATERAL VENTRICLE (DIENCEPHALON) 

LATERAL VENTRICLES (SUB CORTICAL AREAS-CEREBRUM) 

LATERAL 3 RD (VENTRICLES-CERE FLUID) 

LATERAL 4 TH (VENTRICLES-CERE FLUID) 

LENS (EYE) 

LENTICULA NUCLEUS (BASAL NUCLEI-CEREBRUM) 

LENTICULA NUCLEUS (DIENCEPHALON) 

LONGITUDINAL FISSURE (MAJOR FISSURES-CEREBRUM) 

LUMBAR CISTERN (SUBARACHNOID SPACES-CERE FLUID) 

LUST (EMOTION) 

MALLEUS (MIDDLES EAR-EAR) 

MAMMILLARY BODIES (RELATED STRUCTURES-BRAIN STEM) 

MEDICAL RETICULOSPINAL (MOTOR NERVES) 

MEDICAN/LATERAL APERTURES (CERE FLUID) 

MEDULLARY PYRAMIDS (MOTOR NERVES) 

MIDDLE CEREBELLAR PEDUNCLES (HINDBRAIN-BRAIN STEM) 

104


MIDDLE CEREBELLAR PEDUNCLES (MYELENCEPHALON-BRAIN STEM) 

MOTOR AREA (FRONTAL LOBE-CEREBRUM) 

MOTOR CELL BODIES (SPINAL CORD-SPINAL NERVES) 

MOVEMENT (SENSORY) 

MUSCLES OF THE EYEBALL (EYE) 

MUSCULAR BRANCH (MOTOR NERVES) 

MUSCULAR BRANCHES (MOTOR NERVES) 

NERVE FIBERS (EQUILIBRIUM: CRISTA-EAR) 

NERVE FIBERS (EQUILIBRIUM: MACULA-EAR) 

NERVE FIBERS (TASTE BUDS-TASTE) 

NERVES OF HEAD & FACE (PERIPHERAL SPINAL NERVES) 

NERVES OF LOWER LIMBS (PERIPHERAL SPINAL NERVES) 

NERVES OF THORAX (PERIPHERAL SPINAL NERVES) 

NERVES OF UPPER LIMBS (PERIPHERAL SPINAL NERVES) 

105

ORIENTAL HERBAL PHILOSOPHY 

The Chinese did not have a system of succussion, nor did they have a 

system of homeopathic dilution, but their pharmacology was much akin 

to homeopathic processes. Many herbs were diluted to find safer levels of 

activity. This titration allowed for strong herbs to be used more safely. 

The Chinese have studied the medicinal effects of herbs for thousands 

of years. Specific directions were developed on how to pick the herbs, 

preserve the herbs, and how to prepare the herbal remedy. Often, these 

remedies were made in dilute quantities, sometimes as low as one part 

per trillion, which is equivalent to a 9x. They understood how certain 

herbs could be made more dilute and still achieve pharmacological 

effectiveness. Nature provides many energetic factors beyond mere 

chemistry. Subtle energetic effects, mineral balance, electrical regulation 

abilities, and more are stable in dilution. Dilution also offers safety in 

compliance with the minimal dose concept of medicine. Many Chinese 

herbs have excellent effects in low-potency homeopathic form. 

The Dr. Recommends’ oriental herb remedies combine the compatibility of 

herbology and homeopathy. This is to insure safety first, while 

guaranteeing effectiveness. Many compounds can be increased in 

energetic potency as we make them more and more dilute, while 

preserving their activity. The oriental herb formulas are quality controlled 

through QQC TM techniques. 

Source: http://www.myhealthandharmony.com/category_s/33.htm 

106

Quality of Herbs 

America has often come under fire because of an inability to supply 

good quality herbs. This is largely due to the fact that American herbs 

can be picked at any time, in any place. In following the Chinese 

protocol, herbs are picked at precise times and in precise ways so that 

the pharmacological activity of the herb is preserved. Dr. Recommends 

buys many of its herbs from the Chinese, Japanese and Korean markets. 

Still, that is not enough; each of these herbs must undergo quality 

control methods to make sure that the pharmacological activity of the 

herb is above the satisfactory level and at the highest level of potency in 

developing the natural pharmaceuticals. 

Next in developing quality control techniques beyond the chemistry 

and beyond the range of 12x, Dr. Recommends developed Kirlian 

photography methods of analysis, freezing studies of the crystalline 

structure of the liquid crystal effect of water, trivector analysis to analyze 

the magnetic, dielectric static and conductance fields of the different 

homeopathics to understand the energetic nature of these compounds; 

and patient reactivity modes, challenging them on skin resistance, 

voltage, and other directed activity. As well, Dr. Recommends has 

researched a photo-multiplier, and has measured the photons coming off 

of these fields; and how these different compounds affect living tissue 

with their electromagnetic radiation through the mitogenic process. 

The development of a quality control process was paramount in 

developing a way to create the most precise, safe and effective remedies 

for doctors to use with their patients. 

Dr. Recommends realized that this needed to have a global expression, 

and has developed manufacturing in Ireland and Canada. Dr. 

Recommends has developed a global strategy to supply doctors and 

practitioners throughout the USA, Europe, and Canada with product, 

107

guaranteeing the safety and effectiveness, the reverence for nature, and 

the education. Current seminar development is happening in all of these 

countries; educating doctors in how to develop diagnostic protocol and 

healing therapeutic regimes for their patients, using these natural 

products. 

For the doctor who wants natural, homeopathic pharmaceuticals, Dr. 

Recommends is ready to serve with the highest level of quality and 

service all directed through the company pledge for safety, effectiveness, 

quality control, natural healing, reverence of nature, and education of 

both patient and doctor. Dr. Recommends welcomes you to a new 

standard and level of quality control and service. 

108

ORIENTAL HERBAL REMEDIES 

ANTHELMINTIC (1 fl. oz.) 


Indication: Purgative for worms and intestinal parasites 

Ingredients: Meliae Toosendan Fructus, Quisqualis Fructus, Cucurbitae 

Semen, Torreyae Semen, Omphalia, 3x, 6x, 12x, 30x. 

ANTI-ASTHMATIC (1 fl. oz.) 


Indication: Wind and cold effects, chills and fever, Exterior symptom 

complex, Regulates energy for lungs 

Ingredients: Perillae Folium, Astragali Radix, Ephedrae Herba, 

Cinnamomi Cortex, Armeniacae Semen, Glycyrrhizae Radix, Paeoniae 

Radix, Zizyphi Fructus 3x, 6x, 12x, 30x. 

ANTI-PHLOGISTIC (1 fl. oz.) 


Indication: Protects body from wind, cold, dampness, Improves chi 

Ingredients: Schizonepetae Herba, Ledebouriellae Radix, Notopterygii 

Rhizoma, Angelicae Dahuricae Radix , Ligustici Rhizoma, Bupleuri Radix, 

Peucedani Radix, Platycodi Radix, Poria, Menthae Herba, Glycyrrhizae 

Radix, Aurantii Fructus 3x, 6x, 12x, 30x. 

ANTI-PYRETIC (1 fl. oz.) 


Indication: Fever, Febrifugal, Expels toxic heat, wind, chills from exterior 

Ingredients: Forsythiae Fructus, Menthae Herba, Platycodi Radix, 

Lonicerae Flos, Schizonepetae Herba, Arctii Fructus 3x, 6x, 12x, 30x. 

ANTI-RHEUMATIC (1 fl. oz.) 


Indication: Dispels wind, cold, dampness to improve rheumatic pain, 

Activates blood flow in collateral channels 

Ingredients: Aconiti Carmichaeli Preparata Radix, Angelicae Dahuricae 

Radix, Olibanum, Myrrha, Lumbricus, Clematidis Radix, Draconos Os 

3x, 6x, 12x, 30x. 

109

BLOOD (1 fl. oz.) 


Indication: Replenishes blood, Restores vitality, Maximizes acupuncture 

system development of blood 

Ingredients: Ginseng Radix, Rehmanniae Radix, Angelicae Dahuricae 

Radix, Atractylodis Lanceae Rhizoma, Cinnamomi Cortex, Paeoniae 

Radix, Arctii Fructus, Trifolium pratense, Spinacea oleracea 3x, 6x, 12x, 

30x. 

BONE (1 fl. oz.) 


Indication: Degenerative conditions, Unstable chi 

Ingredients: Myrrha, Lonicerae Flos, Scutellaria lateriflora, Taraxacum 

officinale, Magnoliae Officinalis Cortex, Juglans nigra, Tang Kuei, 

Akebiae Caulis Fructus, Echinacea purpurea, Shark Cartilage, Sarcode: 

Bone/Bone Marrow, Equisetum arvense, Beta vulgaris 3x, 6x, 12x, 30x. 

CARMINATIVE (1 fl. oz.) 


Indication: Relieves gas and stagnation of food, Dispels congestion of 

toxic energy from stomach and bowels 

Ingredients: Citri Immaturi Pericarpium, Magnoliae Liliflorae Flos, 

Linderae Radix, Rhei Rhizoma, Pharbitis Semen 3x, 6x, 12x, 30x. 

COLD AND FLU (1 fl. oz.) 


Indication: Colds, Flu, Expels heat, cold and wind from interior 

Ingredients: Lonicerae Flos, Forsythiae Fructus, Arctii Fructus, Menthol, 

Glycerinum, Glycine, Schizonepetae Herba, Echinacea purpurea, 

Placenta, Zingiber officinale 3x, 6x, 12x, 30x. 

DIGESTIVE STIMULATOR (1 fl. oz.) 


Indication: Invigorates stomach, spleen, lung, heart, Reinforces middle 

burner 

ngredients: Ginseng Radix, Codonopsis Pilosulae Radix, Astragali Radix, 

Glycyrrhizae Radix, Hordei Germinatus Fructus, Atractylodis Lanceae 

Rhizoma, Polygonati Rhizoma 3x, 6x, 12x, 30x. 

ESOPHAGUS (1 fl. oz.) 


Indication: Degenerative conditions, Unstable chi, Balances upper 

warmer 

Ingredients: Salvia officinalis, Scutellaria Barbatae Herba , Zizyphi 

Fructus, Rhei Rhizoma, Achyranthis Radix, Zingiber officinale, 

Ammonium Nitricum 3x, 6x, 12x, 30x. 

110

EXPECTORANT (1 fl. oz.) 


Indication: Clears lungs of mucous, Dispels heat in lungs 

Ingredients: Anemarrhenae Rhizoma, Mori Radicis Cortex, Trichosanthis 

Semen, Gardeniae Fructus, Poria, Citri Immaturi Pericarpium 3x, 6x, 

12x, 30x. 

FEMALE (1 fl. oz.) 


Indication: Regulates menstrual disturbances, Restores vitality and 

energy to blood of female 

Ingredients: Codonopsis Pilosulae Radix, Atractylodis Lanceae Rhizoma, 

Angelicae Dahuricae Radix, Rehmanniae Radix, Poria, Cyperi Rhizoma, 

Zizyphi Fructus, Ligustici Rhizoma, Glycyrrhizae Radix 3x, 6x, 12x, 30x. 

HEPATIC (1 fl. oz.) 


Indication: Removes stagnant energy from liver, Restores liver chi 

Ingredients: Magnoliae Officinalis Cortex, Curcumae Rhizoma, 

Aquilariae Lignum, Verbena hastata, Bupleuri Radix, Corydalidis Tuber 

3x, 6x, 12x, 30x. 

HYPERTENSIVE (1 fl. oz.) 


Indication: Alleviates heat in liver, Corrects deficiency in yin of liver, 

Balances excess yang 

Ingredients: Haematitum, Pinellia Tuber, Achyranthis Radix, Rauwolfiae 

Verticillatae Radix 3x, 6x, 12x, 30x. 

KIDNEY (1 fl. oz.) 


Indication: Degenerative conditions, Unstable chi, Removes toxic energy 

from ancestral meridians. 

Ingredients: Lobelia inflata, Imperatae Rhizoma, Dioscorea batatis 

Rhizoma, Lygodii Spora, Desmodii Herba, Haematitum, 

Cirsii Japonica 3x, 6x, 12x, 30x. 

LARGE INTESTINE (1 fl. oz.) 


Indication: Degenerative conditions, Unstable chi, Removes wind from 

large intestine 

Ingredients: Oldenlandiae Herba, Lonicerae Flos, Scutellaria Barbatae 

Herba, Taraxacum officinale, Sophorae Flos, Sanguisorbae Radix, 

Magnoliae Officinalis Cortex, Akebiae Caulis, Citrus trifoliata, Salviae 

Miltorrhizae Radix 3x, 6x, 12x, 30x. 

111

LAXATIVE (1 fl. oz.) 


Indication: Relieves constipation due to spleen fluid deficiency, Dispels 

toxic energy from large intestine, Boosts liver chi 

Ingredients: Cannabis Semen, Rhei Rhizoma, Armeniacae Semen, 

Magnoliae Officinalis Cortex, Rhamnus purshiana , Capsicum 

frutescens, Rhei Rhizoma 3x, 6x, 12x, 30x. 

LIVER (1 fl. oz.) 


Indication: Degenerative conditions, Unstable chi, Removes toxic energy 

liver 

Ingredients: Archangelica , Salviae Miltorrhizae Radix, Carathami Flos, 

Scutellariae Barbatae Herba, Echinopsis Radix, Akebiae Caulis, Paeoniae 

Radix, Gardeniae Fructus, Amoni Semen, Angelica Sinensis 3x, 6x, 12x, 

30x. 

LUNG (1 fl. oz.) 


Indication: Degenerative conditions, Unstable chi, Removes heat from 

lung 

Ingredients: Mori Folium, Coicis Semen, Trichosanthis Radix, 

Sargassum, Pumex, Houttuyniae Herba, Armeniacae Semen, Laminariae 

Thallus, Lepidii Semen, Stemonae Radix, Salviae Miltorrhizae Radix, 

Glycyrrhizae Radix, Imperatae Rhizoma 3x, 6x, 12x, 30x. 

LYMPH (1 fl. oz.) 


Indication: Degenerative conditions, Unstable chi, Removes excess yin 

from interior 

Ingredients: Myrrha, Aconiti Carmichaeli Praeparata Radix, Angelicae 

Dahuricae Radix, Ephredrae Herba, Echinacea purpurea 3x, 6x, 12x, 

30x. 

MENTAL (1 fl. oz.) 


Indication: Invigorates kidney meridian, Senility, Old age, Balances 

excess yin 

Ingredients: Cornu Cervi, Hippocampus, Epimedii Herba, Ginseng Radix, 

Cynomorii Herba, Angelicae Dahuricae Radix 3x, 6x, 12x, 30x. 

112

PREVENTATIVE (1 fl. oz.) 


Indication: Tonifies and improves immunity, Balances yin and yang 

irregularities 

Ingredients: Wisteria chinensis, Trapa natans, Terminalia Chebulae 

Fructus, Coicis Semen 3x, 6x, 12x, 30x. 

SEDATIVE (1 fl. oz.) 


Indication: Nourishes blood of liver, Expels heat from heart, Fatigue, 

Insomnia 

Ingredients: Coptidis Rhizoma, Cinnabaris, Valeriana officinalis, Zizyphi 

Fructus, Glycyrrhizae Radix, Zizyphi Spinosi Semen, Tritici Fructus 3x, 

6x, 12x, 30x. 

STOMACH (1 fl. oz.) 


Indication: Degenerative conditions, Unstable chi, Balances middle 

warmer 

Ingredients: Solanum nigrum, Salviae Miltorrhizae Radix, Scutellariae 

Barbatae Herba, Pteris Herba, Raphni Semen 3x, 6x, 12x, 30x. 

UTERINE (1 fl. oz.) 


Indication: Degenerative conditions, Unstable chi 

Ingredients: Cinnamomi Cortex, Carthami Flos, Phellodendri Cortex, 

Ostraea Testa, Astragali Radix, Lonicerae Flos, Gentianae Scabrae Radix, 

Aconiti Carmichaeli Praeparata Radix, Linderae Radix, Violae Herba 3x, 

6x, 12x, 30x. 

113

CHINESE-AMERICAN HERBALS 

Achyranthes 

Aconite (Processed) 

Aconite (Roasted) 

Akebia 

Anemone 

Angelica 

Anteater Scales 

Apricot Seed 

Arctium 

Areca Seed 

Asparagus 

Astragalus 

Cardamon 

Carthamus 

Centipeda 

Chih-Shih 

Chrysanthemum 

Cirsium 

Clematis 

Coix 

Cyperus 

Cuttle Bone 

Dioscorea 

Dragon Bone 

Fennel 

Forsythia 

Gardenia 

Gentiana 

Glehnia 

Haematite 

Hoelen 

Houttuynia 

Imperta 

Jujube 

Laminaria 

Leonurus 

Lepidium 

Licorice 

Lily 

Lindera 

Lonicera 

Lotus Embryo 

Lotus Receptacles 

Lotus Seed 

Lycium Fruit 

Lygodium 

Magnolia Bark 

Magnolia Flower 

Malt 

Mentha 

Morus Bark 

Morus Branch 

Morus Leaves 

Myristicae 

Myrrh 

Oldenlandia 

Omphalia 

Oryza 

Peony 

Phellodendron 

Placenta 

Plantago 

Pumice 

Pyrite 

Raphanus 

Rauwolfia 

114 

Rhubarb 

Salvia 

Sanguisorba 

Sargassum 

Schizandra 

Schizonepeta 

Scute 

Scute Herba 

Smilax 

Sophora 

Stemona 

Sterculia 

Tang-Kuei 

Terminalia 

Thlaspi 

Thymifolia 

Trichosanthes Fruit 

Trichossanthes Seed 

Tsao-ko 

Tsao-Tou-Kou 

Tussilago 

Viola 

Xanthium 

This is a brief list of the most used Chinese herbal homeopathics. 

Others are available upon request made as homocords (3x, 6x, 12x, 30x) 

of the herbal.

CHINESE HERBOLOGY AND HOMEOPATHY 

In the chapter on the scientific explanation of homeopathy it was 

explained that there are several different pharmacological dynamics 

which allowed for homeopathy to occur at low-dose ratios; those of 12x 

or below. 

The Arndt-Schultz law indicated how poisons in certain compounds 

would have a paradoxical shift in activity as they were made more and 

more dilute. This means that whatever the effect of a poison is in raw 

dose, as it is made more and more dilute there is a paradoxical shift, or a 

reversal of what the compound does. 

As we have proved several times in the Quantum Biology, the Quantum 

Biology Workbook, and other publications, homeopathy is not just like 

treating like. Oftentimes homeopathy is treating via the pharmacological 

agent within the herb. Thus the indications of the homeopathic remedy 

are very similar, if not identical to the indications suggested by the active 

ingredients of the original herb. With this in mind, just what is 

homeopathy vs. allopathy? To offer a new definition for homeopathy 

which encompasses the old definition, we can see that a homeopath is 

truly trying to stimulate the organism of the human body to respond and 

heal itself. In allopathy, an outside intervention via a drug is meant to 

sedate, stimulate, block, deceive, or do some type of unnatural process. 

Thus, the organism becomes dependent on the outside stimulus, such as 

when an MAO inhibitor is used to stop depression; the person’s own 

development of monoamine oxidase becomes deficient. If we use an anti- 

histamine to fight histamine release, then the person’s own development 

of histamine can be deficient. 

Allopathy seeks to build dependence. The key for the allopath is the 

hope that the allopathic medication will pick up some slack, and that the 

patient will heal himself while the allopathic medication is operating. In 

other words, he hopes that the patient can find his own biological 

115

solution while the anti-histamine is working. But the anti-histamines 

and most of the allopathic synthetic medications, of course, do not cure; 

they only stimulate externally, relying on the forces of nature to cure the 

body in the interim. 

In homeopathy, there are many different principles at play that are 

trying to encourage the body to heal itself, rather than stimulating it to 

heal itself. This is the concept of the minimal dose which Hahnemann 

believed in; trying to find the smallest amount of a homeopathic or 

pharmacological agent that could gently nudge the patient back into the 

biological cybernetics of health. Using a “feather” to stimulate such a 

balance is the principle of homeopathy. 

In using the Arndt-Schultz law for poisons such as Belladonna, Apis 

mellifica, Hepar sulph, etc., we can see that this principle illustrates that 

what a poison does in raw dose is opposite to a homeopathic form of the 

poison. It can be observed in snake venoms and other biological poisons 

that they have the ability to mend and heal different enzyme pathways. 

In herbs which are not poisons, we can also see a homeopathic 

principle where a compound is used to apply a gentle nudge to the 

patient to return to health. In Chinese herbalism, if a patient had too 

much heat in the body, such as fever, the herbalist would use a 

refrigerant. If a patient had a problem with constipation, then an herbal 

laxative would be used. 

We see these different propositions as being akin to homeopathy in 

that we would try to use the least possible amount of refrigerant or 

whatever product to accomplish the job of bringing the patient back to 

stability, just as a homeopath might use Eyebright, or might use adrenal 

tissue to help in a weak adrenal case. This is also applied to the concept 

of Chinese herbalism. 

The new definition of homeopathy is one of gentle stimulation of the 

body to heal itself rather than to be dependent on an outside 

pharmacological intervention. This broader definition of homeopathy will 

116

allow us to re-evaluate the different herbals and natural compounds that 

used to be in the natural compendium, and bring them back into the 

medical repertoire. In using the different compounds of the herbal 

repertoire we can see that this is much akin to a homeopathic 

philosophy. The dilution process is merely to seek a minimal dose of 

these items, so that we can accomplish the positive effects and minimize 

the negative effects of the herbs. Thus, homeopathy allows for many 

different factors: 

1) Homeopathy can be nutritional supplementation. If we use a 

homeopathic compound such as Vitamin A or Vitamin B to supplement 

the body’s deficiency syndrome, then homeopathy can be used in a 

nutritional sense. If we were to take a concentrated source of B-12 and 

dilute it one part to ten, six times, to arrive at a 6x, we would see that 

this 6x is approximately equal to the RDA of B-12. Some of the minute 

doses of vitamins that people use can be reflected in the compounds of 

homeopathy. Such homeopathic compounds made for nutritional 

supplementation are in the Liquitrophic line made by Dr. Recommends. 

These different liquitrophic were developed for nutritional 

supplementation in using the minimal dose philosophy, and also using 

the highest quality of vitamins known to man; that of vitamins made by 

nature, not the synthetic vitamins made by man’s technology. This line 

was basically a variation of Royal Lee’s ideas of protomorphology and 

nutrition using natural compounds such as snow pea for kidney 

development, wheat grass for B Vitamins, natural wheat germ for 

Vitamin E, and the whole series of natural Vitamin C factors for Vitamin 

C. These compounds have been blended into natural liquids for vitamin 

supplementation, and are a superior line to some of the Standard 

Process Formulas. The Standard Process Formulas use different 

unnatural pills, as nature does not provide pill trees and capsule bushes. 

Using these liquids, we can increase the surface area over one million 

times. We can start the digestive process in the mouth with the help of 

117

the brain and all the innervations that go into the nasal pharynx, so that 

the nervous system can properly prepare for absorption and utilization. 

By doing this, it has been possible to increase the effectiveness and the 

mode of delivery of the Standard Process Formulas while capturing an 

increase in the potency. 

2) Homeopathy can be used to help stimulate the body. So if we use 

caffeine or Belladonna at low dose, we can achieve some of the low-dose 

pharmacological action; trying to trigger the body to do its own healing. 

The vast difference here between homeopathy and allopathy is that we do 

not try to incur dependence with homeopathy, but rather use the 

minimal dose, and gently shift the patient to being able to accomplish his 

own health. 

3) Homeopathy can be used in many classic ways to help reverse 

symptoms, and stimulate the body to return to the balance of its 

cybernetic systems. This chapter is dedicated, however, to the idea of 

using herbs in high concentrations and low potencies of 2x, 3x, and 4x 

for pharmacological and homeopathic action. 

Let us return to the analysis of the Chinese herb philosophy. 

Belladonna contains atropine, and the pharmacological effects of it are 

that it makes us red as a beet, dry as a bone, and mad as a hatter. This 

is the anti-cholinergic effect of the pharmacology of the atropine in the 

Belladonna compound. Belladonna is a poison. If taken in large enough 

doses it will cause death. If we make the Belladonna solution more and 

more dilute, and more and more dilute, we will see, if we chart the 

pharmacological effects of Belladonna, that at a certain point it will cause 

a paradoxical shift, and it will reverse redness, reverse dryness, and 

reverse madness. Thus, if a patient were to come to us who was red as a 

beet, dry as a bone, and mad as a hatter, we might suggest a 6x, 9x, or 

possibly higher potencies of Belladonna to reverse these processes. 

The Arndt-Schultz law, as pointed out in the chapter on pharmacology, 

states that a compound that is a poison will always have a reversal. A 

118

compound that is not a poison will follow Wilder’s Law of Initial Values. 

This tells us that as a nonpoisonous compound is made more dilute we 

might see an increase in its pharmacological activity of what the raw 

dose of the formula does, we might see an inverse, or we might see no 

effect whatsoever. An example of this would include most of the sarcodal 

tissues including thyroid and adrenal. Here we will see that the effect of 

these sarcodal tissues is stimulation or a hormonal effect. If we use raw 

adrenaline, we will see that it has a stimulating effect on the body. If we 

use a more and more dilute form of the adrenaline - 6x, 12x, etc., we will 

often see a similar increase in the same type of stimulation capacity. We 

rarely see reverses in the sarcodal formulas. 

Many herbs also follow this potentiation cycle, such as Eyebright, 

which if taken in raw doses makes the eyes bright; hence its name. It 

was named Eyebright because herbalists found that it helped conditions 

of the eye. As we make it more and more dilute we see that the 

homeopathic use of Eyebright, even in dilute quantities of 16x, 30x, and 

above, will help improve eyes and vision. If it were all reversal, we would 

only use Eybright when a patient came in whose vision was too good. If a 

patient said, “I see too well,” then homeopathic Eyebright would be used. 

But this is not the case; homeopathic Eyebright is used to improve 

vision. Many herbs have increased or equal health value in homeopathic 

form. It is wrong to merely value compounds by their dosages, as in 

synthetic pharmacology. Many Chinese herbs can have excellent effects 

in low-potency homeopathic form. 

As stated in the Law of Initial Values, some things will be reversal if 

they tend towards poisons, and some things will be potentiating of their 

original effects. Also, some items will have no effect at all as they are 

made more and more dilute. 

In the study of Chinese herbalism, we see a very profound description 

of an excellent natural pharmacology. We can see that the Chinese have 

studied the medicinal effects of herbs for thousands of years, and that 

119

specific directions were developed in how to pick these herbs, preserve 

them, and then prepare certain remedies. Often these remedies were 

made in dilute quantities, sometimes as low as one part per trillion, 

which is equivalent to a 9x. The Chinese understood how certain items 

could be made more dilute and still achieve pharmacological 

effectiveness. To assume that the only active ingredients are chemical in 

these Chinese herbs is to make the same mistake the synthetic chemical 

companies make. Nature provides many energetic factors beyond mere 

chemistry. Subtle energetic effects, mineral balance, electrical regulation 

abilities, and more are stable in dilution. Dilution also offers safety in 

compliance with the minimal dose concept of medicine. 

The Chinese did not have a system of succussion, nor did they have a 

system of homeopathic dilution, but their pharmacology was much akin 

to some of these processes. Many herbs were diluted to find safer levels 

of activity. This titration allows for strong herbs to be used safely. 

One of the problems of the herbal industry in America is the lack of 

preciseness in how an herb should be picked and processed. In China, 

an herb is picked at precise times of the year using precise methods, so 

that the pharmacological activity of the herb is assured. In America, 

however, the herbal industry for the last fifty years has been much less 

precise. Without a precise pharmacopoeia, unknowing American 

distributors of herbs might pick them at non-pharmacologically active 

periods of their cycle. Without care for quality control, many companies 

pass on irregular or impotent products without safety or efficacy. This 

has led to the demise of the herbal industry in America; whereas, the fine 

quality control processes of the herbs in China has led to the high 

success of China’s sphere of medical influence. In 1962, the FDA 

abolished the natural compendium of herbs and natural remedies. We 

might look at several theories for its demise, but indeed, some of this 

lack of quality control is a factor. 

120

In developing an herbal protocol to mix with homeopathics, wise 

manufacturers including Dr. Recommends have had to develop severe, 

exacting quality control criteria for accepting different herbals ordered 

from American or other herbal suppliers. These types of quality control 

techniques include product surveys, product assays, and product 

determination in methods such as spectrophotometer, atomic 

absorption, chromatography, culture analysis, and other forms of 

chemical procedures to determine pharmacological activity. Dr. 

Recommends has been able to develop the finest quality control analysis 

protocol to assure the highest form of potency for the different herbs 

utilized. 

The Chinese literature is filled with herbal references, and information 

about how these herbs can be used medicinally to help patients in a wide 

variety of ways. It is Dr. Recommends’ idea that many of these herbs can 

also be put into homeopathic dilution, and used in a similar process. 

This is to insure safety first while guaranteeing effectiveness. We do not 

see this as contradictory to the homeopathic process in any way. In fact, 

Wilder’s Law of Initial Values tells us that many of these compounds, 

once understood, can be increased in energetic potency as we make them 

more and more dilute, while preserving activity. Dr. Recommends has 

developed a pilot study and statistical protocols to determine the 

absolute effectiveness and safety of the different compounds. Clinical 

trials are an important part of the Dr. Recommends’ quality control 

protocol. 

Dr. Recommends started with the idea that Chinese herbology and 

homeopathy were compatible in their format, and could be blended. The 

first type of blending in this technology was through a system of oriental 

herb formulas directed toward different organ systems, which were called 

“Oriental Herbs for Organs”. A list of these different products is included. 

121

These were taken from the book, Treating Cancer with Chinese Herbs, by 

Hong-Yen Hsu. In this book, several cancer treatment modalities were 

noted for a variety of different organ system types of cancer. These 

treatment modalities were developed by doctors in Shanghai, China. 

They used many different types of herbal therapies which Dr. 

Recommends sought to blend into formulas for treatment of similar 

degenerative problems. 

After twenty-five years of commerce with these products, the remarks 

by many doctors have confirmed that this is not only a safe system of 

treatment, it is a very effective one as well. The herbs in those different 

formulas were put into formulas at low potencies of 2x, 3x, and 

sometimes 4x, equivalent to the dilution methods used by the doctors in 

China. In fact, the dilutions are almost equivalent to the treatments used 

in China. 

The success of these formulas has led Dr. Recommends to develop 

other formulas following the Chinese herbal system. These are developed 

with the Chinese herbal acupuncture modality of treatment. In 

developing these herbal formulas, Dr. Recommends tries to use herbal 

remedies from all over the world, including those from the Amazon rain 

forest where certain herbs have been studied and used by Amazon tribes 

for years. In making up these formulas, Dr. Recommends has used herbal 

formulas from the Amazon, China, Korea, America, South America, 

Europe, Russia, and many other places. 

Bibliography 

Lee, R. Hanson, W. Protomorphology. Lee Foundation for Nutritional 

Research, 1947. Milwaukee, Wisconsin. 

Hsu, Hong-Yen. Treating Cancer with Chinese Herbs. The Oriental 

Healing Arts Institute, 1982. Long Beach, California. 

122

THE MIASM PHILOSOPHY 

In classical homeopathy, a miasm is thought to be a tendency toward a 

disease pattern that is passed on from one generation to the next. 

Sometimes, these disease tendencies can produce a variety of conditions 

that can be inherited from our ancestors. Hahnemann found that 

miasms such as sycosis (a type of gonorrhea), syphilis, and psora, could 

be transmitted through genetic inheritance. We now know that there are 

other types of miasm links. Miasms work on very high vibrational levels; 

thus, the miasm formulas need to be in a very high homochord state to 

help in breaking up the miasm tendency in the patient. This is achieved 

through the QQC TM process. 

We caution the young initiate in homeopathy; using these remedies 

takes some degree of skill and training. 

123

MIASM REMEDIES 

MIASM-ALLER (1 fl. oz.) 


Indication: Allergies 

Ingredients: Encephalitis, Typhus, Malaria, Anthrax, Toxoplasmosis, 

Venereum, Cold Virus, Allergic Reactivity Sarcodes: Adrenal, Pancreas, 

Liver 12x, 30x, 100x, 500x, 1000x. 

MIASM-CAN (1 fl. oz.) 


Indication: Degenerative diseases 

Ingredients: Melanoma, Sarcoma, Myeloma, Neurofibroma, Carcinoma, 

Tumor 12x, 30x, 100x, 500x, 1000x. 

MIASM-CF (1 fl. oz.) 


Indication: Chronic fatigue, Tiredness, Exhaustion 

Ingredients: Brucellosis, Epstein Barr, Mononucleosis, Cytomegalovirus, 

Tularemia, Streptococcus fecalis, Elephantiasis, Coxsackie, 

Neuromyasthenia, Candida albicans 12x, 30x, 100x, 500x, 1000x. 

Echovirus 12x, 17x, 30x, 100x, 500x, 1000x. Pseudomonas 12x, 17x, 

30x, 100x, 500x, 1000x. Borrelia burgdorferi 13x, 30x, 100x, 500x, 

1000x. Malaria, Pestinum 15x, 30x, 100x, 500x, 1000x. Spirillum 

minus 16x, 30x, 100x, 500x, 1000x. 

MIASM-CHOL (1 fl. oz.) 


Indication: Cholera, Intestinal disorders 

Ingredients: Ameba 15c, 30c, 100c; Cholera, Dysentery (Bacillus 

dysenteriae), Pyrogenium, 20x, 30x, 100x, 500x, 1000x. 

MIASM-FNG (1 fl. oz.) 


Indication: Fungus, Yeast sensitivity 

Ingredients: Amanita muscaria, Saccharomyces, Candida albicans, 

Molds, Epidermophyton, Chlamydia 12x, 30x, 100x, 500x, 1000x. 

Blastomyces 17x, 30x, 100x, 500x, 1000x. Candida parapsilosis 19x, 

30x, 100x, 500x, 1000x. 

124

MIASM-LEP (1 fl. oz.) 


Indication: Leprosy, Skin disorders 

Ingredients: Leprosy, DNA, RNA, Myrrh, Verbascum thapsus 12x, 30x, 

100x, 500x, 1000x. 

MIASM-MEN (1 fl. oz.) 


Indication: Mental disorders 

Ingredients: Encephalitis, Nocardia, Bacteria, Virus, Imponderables: 

Guilt, Shame, Jealousy, Rage, Hatred, Prejudice, Incest, Greed, 

Judgmental, Obsession, Depression, Aggression 12x, 30x, 100x, 500x, 

1000x. Meningitis, Trichinosis 15x, 30x, 100x, 500x, 1000x. 

MIASM-MZL (1 fl. oz.) 


Indication: Measles, Dermatitis 

Ingredients: DNA, RNA, Chamomilla, Trifolium pretense, Pulsatilla 12x, 

30x, 100x, 500x, 1000x; Morbillinum (Rubeola) 20x, 30x, 100x, 500x, 

1000x. 

MIASM-PSO (1 fl. oz.) 


Indication: Psora, Skin disturbances 

Ingredients: Psorinum, Staphylococcus, Streptococcus, Tuberculinum, 

DNA, RNA, Calcarea Carbonica, Medorrhinum, Kali Muriaticum, 

Pulsatilla, Bryonia 12x, 30x, 100x, 500x, 1000x. 

MIASM-SYC (1 fl. oz.) 


Indication: Sycosis, Skin disorders 

Ingredients: Syphilinum, Nocardia, DNA, RNA, Natrum Muriaticum, 

Petroleum, Sulphur, Natrum Sulphuricum, Zincum Valerianicum, Apis 

mellifica 12x, 30x, 100x, 500x, 1000x. Medorrhinum, Chlamydia 

trachomatis 16x, 30x, 100x, 500x, 1000x. 

MIASM-SYP (1 fl. oz.) 


Indication: Syphilis, Skin disorders, Sexual disturbances 

Ingredients: Syphillinum, DNA, RNA, Lymes, Antimonium Crudum, Kali 

Muriaticum, Mercurius Solubilis, Mercurius Vivus, Hepar Sulphuris 

Calcareum 12x, 30x, 100x, 500x, 1000x. 

125

MIASM-TB (1 fl. oz.) 


Indication: Tuberculosis 

Ingredients: Tuberculosis, Pneumonia, Bronchiecyasis, Pertussis, DNA, 

RNA, Natrum Sulphuricum, Aconitum napellus 12x, 

30x, 100x, 500x, 1000x. 

MIASM-TET (1 fl. oz.) 


Indication: Tetanus, TMJ disorders 

Ingredients: Tetanus, TMJ, DNA, RNA, Botulinum, Shigella, Calcarea 

Phosphorica, Calcarea Sulphurica 12x, 30x, 100x, 500x, 1000x. 

MIASM-VAC (1 fl. oz.) 


Indication: Vaccine 

Ingredients: Vaccinotoxinum, Varicella, Parotitis, Polio, Grippe, 

Influenza, Diphtheria, Measles, Tetanus 12x, 30x, 100x, 500x, 1000x. 

MIASM-VIR (1 fl. oz.) 


Indication: Virus sensitivity 

Ingredients: Apium Virus, Ichthyolum, Vaccinotoxinum, Morinum, 

Variolinum, Misc. Influenzinum, Vincetoxicum, Retrovirus 12x, 30x, 

100x, 500x, 1000x. Psorinum 16x, 30x, 100x, 500x, 1000x. 

126

THE PSYCHOLOGICAL PHILOSOPHY 

The Dr. Recommends’ psychological homeopathic formulas use a 

combination of homeopathic ingredients to help stabilize psychological 

conditions found in the patient population. These psychological 

conditions run the range of depression, anxiety, mania, etc. It must be 

pointed out that these patients’ systems are often complicated by other 

allopathic treatment that can diminish the homeopathic results. 

The Dr. Recommends’ psychological remedies are not complete therapy 

in and of themselves. Any type of psychological treatment should include 

a referral to a psychologist, counselor, or other professional trained in 

this area. These remedies are an adjunctive therapy and should never be 

used as a primary or a singular method of treatment. 

127

PSYCHOLOGICAL REMEDIES 

PSY-ADJ (1 fl. oz.) 


Indication: Adjustment disorders 

Ingredients: Ustilago maidis, Antipyrine 2x. Caladium seguinum 3x. 

Digitalis purpurea, Arundo mauritanica, Glonoine, Xerophyllum 

asphodeloides 6x. Anhalonium 12x. Kreosotum 24x. Lachesis mutus 

30x. Phosphorus, Nux vomica 30x, 60x, 100x. 

PSY-ANX (1 fl. oz.) 


Indication: Anxiety 

Ingredients: Oxytropis lambertii 3x. Natrum Muriaticum, Borax 4x. 

Alumina 5x. Causticum 6x. Plumbum Metallicum 8x. Sepia 12x. 

Lilium tigrinum 30x. Chamomilla, Coffea tosta 30x, 60x, 100x. 

PSY-DELR (1 fl. oz.) 


Indication: Delirium 

Ingredients: Chamomilla 1x. Helleborus, Chininum Sulphuricum, 

Passiflora incarnata, Scopolamine 2x. Datura stramonium 3x. 

Aconitum napellus 4x. Ranunculus bulbosus 4x, 30x, 60x, 100x. Rhus 

toxicodendron, Operculina, Kali Bromatum, Absinthium 6x. Lachesis 

mutus 8x. Belladonna 30x, 60x, 100x. 

PSY-DEM (1 fl. oz.) 


Indication: Dementia 

Ingredients: Damiana 1x. Apium graveolens, Calcarea Phosphorica 3x, 

1000x. Hyoscyamus niger 4x. Zincum Metallicum, Phosphoricum 

Acidum, Baryta Carbonica, Calcarea Carbonica 6x. Aurum Iodatum 8x. 

Picricum Acidum 10x. Lilium Tigrinum 12x, 30x. Phosphorus 12x, 30x, 

60x, 100x. Stannum Metallicum, Alumina, Iodium, 30x, 60x, 100x. 

Sulphur, Plumbum Metallicum, Antimonium, Mercurius Vivus, 

Bismuthum Metallicum, Iodium 30x, 60x, 100x, 500x. 

PSY-DEP (1 fl. oz.) 


Indication: Depression 

Ingredients: Vitamin B3, B5, B6 4x. Lithium Carbonicum, CCK 6x. 

Sarcode: Brain 6x, 12x. Caulophyllum thalictroides 12x, 30x. Ignatia 

amara 12x, 30x. Sepia 12x. Serotonin 16x. Mercurius Vivus, Silicea, 

Plumbum Metallicum, Iodium, Sulphur 60x, 100x, 1000x, 2000x. 

128

PSY-DEP/EX (1 fl. oz.) 


Indication: Depression (Extrovert) 

Ingredients: Pulsatilla 3x. Caulophyllum thalictroides 3x, 6x, 12x, 60x. 

Cimicifuga racemosa 6x. Natrum Muriaticum, Ferula asafoetida 12x. 

Lachesis mutus 16x. Sepia 16x, 30x, 60x. CCK 30x, 60x. Agaricus 

muscarius, Silicea 30x, 60x, 100x. 

PSY-DEP/IN (1 fl. oz.) 


Indication: Depression (Introvert) 

Ingredients: Passiflora incarnata 2x. Pulsatilla 3x. Nux vomica 3x, 6x, 

12x, 60x. Natrum Muriaticum 12x. CCK 12x, 30x. Sulphur, Petroleum 

60x. Ruta graveolens, Causticum 30x, 60x, 100x, 200x. 

PSY-DIS (1 fl. oz.) 


Indication: Dissociative disorders 

Ingredients: Cyclamen 3x. Thuja occidentalis, Sepia 6x, 12x. Datura 

stramonium 30x. Anacardium occidentale, Lachesis mutus, Nitricum 

Acidum, Hyoscyamus niger 200x. Cimicifuga racemosa, Gelsemium 

sempervirens 30x, 60x, 100x, 200x. 

PSY-HYS (1 fl. oz.) 


Indication: Hysteria 

Ingredients: Valeriana officinalis, Pulsatilla 2x. Castoreum, Picricum 

Acidum 5x. Asafoetida, Asterias rubens, Ignatia amara, Zincum 

Metallicum 6x. Mygale 9c. Moschus 12x. Alumina, Aurum Metallicum, 

Graphites, Sulphur 30x, 60x, 100x, 1000x 

PSY-MANIA (1 fl. oz.) 


Indication: Mania 

Ingredients: Salix nigra 1x. Murex 3x, 30x. Atropinum 8x, 30x. 

Cantharis 12x. Belladonna 12x, 100x. Panax quinquefolium 20x. 

Absinthium, Aconitum, Baptisia tinctoria 30x. Natrum Muriaticum, 

Spongia tosta, Passiflora incarnata 30x, 60x, 100x, 200x. 

129

PSY-MOOD (1 fl. oz.) 


Indication: Mood disorders 

Ingredients: Chamomilla 1x. Aurum Muriaticum 2x. Borax, Aloe 

socotrina 3x. Capsicum annuum 4x. Agaricus, Baptisia tinctoria, 

Bryonia, Mancinella 6x. Phosphorus 9x. Sulphur, Aluminium 

Metallicum, Stannum Metallicum, Mercurius Vivus, Iodium 30x, 60x, 

100x, 500x, 1000x. 

PSY-PER (1 fl. oz.) 


Indication: Personality disorders 

Ingredients: Echinacea purpurea 3x. Rhus toxicodendron, Podophyllum 

peltatum 6x. Thuja occidentalis 6x, 12x, 30x. Sulphur 30x, 50x. 

Picricum Acidum 60x. Phosphorus, Natrum Muriaticum, Bryonia 30x, 

60x, 100x. 

PSY-SCHZ (1 fl. oz.) 


Indication: Schizophrenia 

Ingredients: Aesculus hippocastanum, Medicago sativa 2x. Helonias 

dioica 2x, 6x. Cypripedium pubescens 4x. Abrotanum, Aethusa 

cynapium 6x. Radium, Sepia 30x. Apis mellifica, Phosphorus, 

Belladonna, Nux vomica 30x, 60x, 100x. 

130

IMPONDERABLE HOMEOPATHY 

Imponderable homeopathy is the science of using different vibrational 

entities and transferring them into a water and diatomaceous earth 

mixture. This mixture acts as a mother tincture, and can absorb negative 

or positive energies if exposed to them for fifteen minutes or longer. 

Thus, if the emotional vibrations of greed are exposed to diatomaceous 

earth and water, it can become a mother tincture of the imponderable 

known as greed. The most famous type of imponderable homeopathy is 

x-ray. X-rays are exposed to diatomaceous earth and alcohol, producing 

a mother tincture. This can then be utilized to detoxify a person who has 

been exposed to radiation. 

Within this range of imponderable homeopathics there is the potential 

to treat a wide range of intellectual, vibrational, and energetic problems. 

Included within this text is a long list of some vibrational homeopathics 

that are used by the Dr. Recommends’ pharmaceutical company. This 

range of imponderable homeopathics can be used with some exciting new 

perspectives on homeopathy. 

Another imponderable homeopathic series is the Bach remedies. These 

remedies were developed by Dr. Edward Bach in England, many years 

ago to help a wide spectrum of emotional issues. These remedies consist 

of flower essences derived from many plants and flowers. 

The science of Bach philosophy is extensive. The preparation of the 

remedies is of the homeopathic manner. The essences are diluted and 

then mixed with water and alcohol for patient consumption. For this 

reason, we have decided to add them to our Repertory and put them into 

this chapter; not because of the nature of their manufacture, but 

because of the nature of their use. 

These flower essences are made in a very rational, scientific way, but 

the process is not entirely comprehensible. Each entity seems to work on 

131

a variety of emotional and physiological functions within the patient. 

Thus, the pattern of work is “imponderable.” 

Aided by new biochemical techniques and a vastly expanded 

understanding of immunology and neurochemistry, researchers have 

recently conducted new scientific studies at leading universities, 

hospital, and research facilities throughout the country, clearly linking 

mental and emotional stress as a primary factor in nearly all physical 

disorders. These studies show that emotions, acting through the brain, 

can affect nervous system function, hormone levels, and immunological 

responses, thereby changing a person’s susceptibility to a host of organic 

illnesses. 

Source: 

http://query.nytimes.com/gst/fullpage.html?sec=health&res=9B06EFDA1E38F937A15 

756C0A965948260&n=Top/News/Health/Diseases,%20Conditions,%20and%20Health 

%20Topics/Cancer 

Stress and related disorders have grown to become a major concern to 

us all. However, stress in and of itself is not the problem. The problem is 

in just how well we handle stress. The more mentally and emotionally 

centered and balanced we are, the more effectively we are able to deal 

with stress in our lives. To this end, we chose to put these remedies and 

their repertory into this section of the book. 

132

BACH REMEDIES 

Agrimony: For those not wishing to burden others with their troubles 

and who cover up their suffering behind a cheerful façade. They are 

distressed by argument or quarrel, and may seek escape from pain and 

worry through the use of drugs or alcohol. 

Aspen: For those who experience vague fears and anxieties of unknown 

origin, they are often apprehensive. 

Beech: For those who while desiring perfection, easily find fault with 

people and things. Critical and at times intolerant, they may overact to 

small annoyances or idiosyncrasies of others. 

Centaury: For those who are over anxious to please, often weak willed 

and easily exploited or dominated by others. As a result they may neglect 

their own particular interests. 

Cerato: For those who lack confidence in their own judgment and 

decisions. They constantly seek the advice of others and may often be 

misguided. 

Cherry Plum: For fear of losing mental and physical control, of doing 

something desperate. May have impulses to do things thought or known 

to be wrong. 

Chestnut Bud: For those who fail to learn from experience, repeating the 

same patterns or mistakes again and again. 

Chicory: For those who are overfull of care for others and need to direct 

and control those close to them. Always finding something to correct or 

put right. 

Clematis: For those who tend to live in the future, lack concentration; 

are daydreamers, drowsy or spacey, and have a halfhearted interest in 

their present circumstances. 

Crab Apple: For those who may feel something is not quite clean about 

themselves, or have a fear of being contaminated. For feelings of shame 

or poor self image. For example, thinking oneself not attractive for one 

reason or another. When necessary, may be taken to assist in 

detoxification; for example, during a cold or while fasting. 

Elm: For those who at times may experience momentary feelings of 

inadequacy, being overwhelmed by their responsibilities. 

133

BACH REMEDIES, cont. 

Gentian: For those who become easily discouraged by small delays or 

hindrances. This may cause self doubt. 

Gorse: For feelings of hopelessness and futility. When there is little hope 

of relief. 

Heather: For those who seek the companionship of anyone who will 

listen to their troubles. They are generally not good listeners and have 

difficulty being alone for any length of time. 

Holly: To be used when troubled by negative feelings such as envy, 

jealousy, suspicion, revenge, vexations of the heart, and states indicating 

a need for more love. 

Honeysuckle: For those dwelling in the past, nostalgia, homesickness; 

always talking about the good old days when things were better. 

Hornbeam: For the Monday morning feeling of not being able to face the 

day. For those feeling that some part of the body or mind needs 

strengthening, and for constant fatigue and tiredness. 

Impatiens: For those quick in thought and action who require all things 

to be done without delay. They are impatient with people who are slow 

and often prefer to work alone. 

Larch: For those who despite being capable, lack self confidence or feel 

inferior. Anticipating failure, they refuse to make a real effort to succeed. 

Mimulus: For fear of known things, such as heights, water, the dark, 

other people, or being alone, etc. 

Mustard: For deep gloom which comes on for apparently no known 

reason; sudden melancholia or heavy sadness which lifts just as 

suddenly. 

Oak: For those who struggle on despite despondency from hardships, 

even when ill and overworked; they never give up. 

Olive: For mental and physical exhaustion, sapped vitality with no 

reserve. This may come after an illness or personal ordeal. 

134


Pine: For those who feel they should do or should have done better, who 

are self-reproachful or blame themselves for the mistakes of others. 

Hardworking people who suffer much from the faults they attach to 

themselves, they are never satisfied with their success. 

Red Chestnut: For those who find it difficult not to be overly concerned 

or anxious for others, always fearing something wrong may happen to 

those they care for. 

Rescue Remedy: The most well known formula in the Back Remedy 

system. It has a positive calming and stabilizing effect in an extremely 

broad range of stressful situations, which include nervousness, anxiety, 

accidents, bereavement, and times of great fright, anguish, and 

desperation. Even minor everyday stresses, such as arguments, taking 

exams, making speeches, job interviews or other similar stressful 

situations are reportedly greatly helped. 

Rock Rose: For those who experience states of terror, panic and 

hysteria; also when troubled by nightmares. 

Rock Water: For those who are very strict with themselves in their daily 

living. They are hard masters to themselves, struggling toward some ideal 

or to set an example for others. This would include strict adherence to a 

living style or to religious, personal, or social disciplines. 

Scleranthus: For those unable to decide between two things, first one 

seeming right then the other. Often presenting extreme variations in 

energy or mood swings. 

Star of Bethlehem: For grief, trauma, loss. For the mental and 

emotional effect during and after a trauma. 

Sweet Chestnut: For those who feel they have reached the limits of their 

endurance. For those moments of deep despair when the anguish seems 

to be unbearable. 

Vervain: For those who have strong opinions and who usually need to 

have the last word; always teaching or philosophizing. When taken to an 

extreme, they can be argumentative and overbearing. 

135


Vine: For those who are strong willed. Leaders in their own right who are 

unquestionably in charge. However, when taken to an extreme they may 

become dictatorial. 

Walnut: Assists in stabilizing emotional upsets during transition periods, 

such as puberty, adolescence, and menopause. Also helps one to break 

past links and emotionally adjust to new beginnings such as moving, 

changing or taking a new job, beginning or ending a relationship. 

Water Violet: For those who are gentle, independent, aloof, and selfreliant, 

who do not interfere in the affairs of others; and when ill or in 

trouble prefer to bear their difficulties alone. 

White Chestnut: For constant and persistent unwanted thoughts, such 

as mental arguments, worries or repetitious thoughts that prevent peace 

of mind and disrupt concentration. 

Wild Oat: For the dissatisfaction with not having succeeded in one’s 

career of life goal. When there is unfulfilled ambition, career uncertainty 

or, boredom with one’s present position or station in life. 

Wild Rose: For those who, for no apparent reason, have resigned 

themselves to their circumstances. Having become indifferent, little effort 

is made to improve things or find joy. 

Willow: For those who have suffered some circumstance or misfortune 

which they feel was unfair or unjust. As a result, they become resentful 

and bitter toward life or toward those who they feel were at fault. 

Source: 

http://www.healingartsspa.com/bach_flower_remedies.htm 

http://bowentherapy.homestead.com/bachflowers.html 

136

AGGRESSION 

ANGER 

ANXIETY 

AUTISTIC 

AWARENESS 

BLUE 

CARELESS 

CHAKRA, BASE 

CHAKRA, BROW 

CHAKRA, CROWN 

CHAKRA, HEART 

CHAKRA, STOMACH 

CHAKRA, THROAT 

CONFUSION 

COSMOS 

50 CYCLES 

60 CYCLES 

75 CYCLES 

100 CYCLES 

150 CYCLES 

DELUSION 

DEPRESSION 

1 ST DIMENSION 

2 ND DIMENSION 

3 RD DIMENSION 

4 TH DIMENSION 







DO 

EELF 

ELF 

FA 

FEAR 

GAMMA RAYS 

GRAVITATION 

GREED 

GREEN 

0-500 HERTZ 

500-1000 HERTZ 

1000-1500 HERTZ 

1500-2000 HERTZ 

VIBRATIONAL REACTANTS 

137 

2000-2500 HERTZ 

2500-3000 HERTZ 

3000-3500 HERTZ 

3500-4000 HERTZ 

4000-4500 HERTZ 

4500-5000 HERTZ 

5000-5500 HERTZ 

5500-6000 HERTZ 

6000-10000 HERTZ 

HESITATION 

HYPER GAMMA RADIATION 

INDIGO 

INFRARED 

JEALOUSY 

JOY (EMOTION) 

LA 

VERTEBRAE 

LEFT SPIN 

LUST 

MI 

MICROWAVE 

NEGATIVE MAGNETIC 

NEGATIVE STATIC 

ORANGE 

PASSIVITY 

POSITIVE MAGNETIC 

POSITIVE STATIC 

POWER 

PROJECTION 

RADIO 

RATIONALIZATION 

RE 

RECKLESS 

RED VISIBLE 

RIGHT SPIN 

SADNESS 

SO 

TI 

ULTRAVIOLET 

VIOLET 

VISIBLE 

WORRY 

X-RAYS 

YELLOW

ALLERSODES 

In treating allergies, it was found that small amounts of allergy-causing 

agents can be used to help reverse the anti-body cascade and other 

allergic factors within the body. This type of desensitization can be used 

with oral antigens or injectibles. Modern medicine has used this type of 

allergy treatment for several decades. Dr. Recommends has developed a 

large range of allersodes including inhalant and food allersodes. Within 

the scope of allersodes there are also phenolics which help break up the 

sensitivities to different phenol rings; bodily secretions, including 

hyluronidase; natural anti-histamines, including adrenaline; and other 

liver enzymes that help the body to naturally reduce allergic reactivity. 

Dr. Nelson has developed a large list of allersodes included here. To see 

the research on the effectiveness of these allergy compounds we point the 

reader to The Experimental Data on Homeopathy. Within this text, it is 

possible to see proof of how allergy homeopathy can be used to 

desensitize our patients. 

138

ANIMAL HAIR (1 oz.) 


Oral Antigen Combination 

Ingredients: Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x. 

1-3 Cyclohexanedione 8x. Cat Hair, Dog Hair, Horse Hair 9x, 12x, 30x, 

60x, 100x, 500x, 1000x. Histaminum 30x, 60x, 100x, 500x. In a 

tincture of purified water and non-allergenic alcohol. 

DAIRY (1 oz.) 




1-3 Cyclohexanedione 8x. Cheeses, Cow's Milk, Goat's Milk, Ice Cream, 

Butter 9x, 12x, 30x, 60x, 100x. Histaminum 30x, 60x, 100x, 500x. In a 


GRAIN (1 oz.) 




1-3 Cyclohexanedione 8x. Wheat, Corn, Barley, Millet, Rice 9x, 12x, 30x, 



MOLD/HOUSE DUST (1 oz.) 




1-3 Cyclohexanedione 8x. Mildew, Molds, Household Dust 9x, 12x, 30x, 



139

OLFACTORY SENSITIVITY (1 oz.) 



Ingredients: Rosa canina flos, Taraxacum officinale, Solidago virgaurea, 

Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x. 1-3 

Cyclohexanedione, Formaldehyde 8x. Miscellaneous Synthetic Aromatic 

Compounds 8x, 12x, 30x, 100x, 1000x. Olfactaid 12x. Formaldehyde 

Dehydrogenase 16x, 30x, 60x. Histaminum 30x, 60x, 100x, 500x. In a 


POLLEN (1 oz.) 




1-3 Cyclohexanedione 8x. Flowers, Trees, Grasses 9x, 12x, 30x, 60x, 

100x, 500x, 1000x. Histaminum 30x, 60x, 100x, 500x. In a tincture of 

purified water and non-allergenic alcohol. 

SULFIDE SENSITIVITY (1 oz.) 



Ingredients: Trifolium pratense, Beta Glucuronidase, Adrenalinum 4x. 

Hyaluronidase 6x. 1-3 Cyclohexanedione 6x. Salicylicum Acidum, 

Salicinum, Sodium Bisulfide, Tartrazine, Monosodium Gluconate 8x, 

12x, 30x, 100x, 1000x. Histaminum 30x, 60x, 100x, 500x. In a tincture 

of purified water and non-allergenic alcohol. 

140

INHALANT REACTANTS 

ACACIA 

ACTINOMYCES ISRAELII 

AGARICUS MUSC. 

ALDER, RED, WHITE 

ALFALFA 

ALLSCALE 

ALERNARIA TENIUS 

ASH, ARIZONA, GREEN, OREGON, WHITE 

ASPEN, QUAKING 

ASPERGILLUS, FLAVUS, FUMIGATUS, GLAUCUS, NIGER, TERRUS 

BAHIA 

BARLEY, CULTIVATED 

BARLEY SMUT, LOOSE 

BAYBERRY 

BEEFWOOD 

BENT, CREEPING 

BERMUDA GRASS 

BIRCH, MIXED, RED, RIVER, WHITE 

BLASTOMYCES DERMATITIDIS 

BLUE, ANNUAL, CANADA, KENTUCKY 

BLUEGRASS 

BOTRYTIS 

BOX ELDER 

BROMEHUNG 

BROMWEED 

CANADA BLUEGRASS 

CANDIDA (MONILA) ALBICANS 

CARELESSWEED 

CEDAR, MOUNTAIN, PINCHOT, RED 

CEPHALOSPORIUM, COMMON, ROSEUM 

CHAETOMIU 

CHESS, SOUTHERN 

CHINESE ELM 

CLADOSPORIUM FULVUM 

CLAVICEPS, PASPALI, PURPUREA 

CLOVER, SWEET 

COCKLEBUR 

CORN, CULTIVATED, POLLEN 

CORN SMUT 

COSMOS 

COTTONWOOD 

COTTONWOOD, MIX, COMMON, ARIZONA, EASTERN, WESTERN 

CRAWLING INSECT 

141

INHALANT REACTANTS, cont. 

CURVALIARIA SPICIFERA 

CYPRESS, BALD, ARIZONA 

DAHLIA 

DANDELION 

DERMATOPHILUS CONGOLENSIS 

DOCK, RUMEX MIX, SOUR, YELLOW 

ELM, AMERICAN, CEDAR, CHINESE, SLIPPERY 

EUCALYPTUS 

FIR, DOUGLAS 

FIREBUSH 

FIVE GRASS MIX 

FLOWER POLLEN 

FLYING INSECT 

FUSARIUM SOLANI 

GELASINOSPORA CEREALIS 

GEOTRICHUM CANDIDUM 

GLIOCLADIUM FIMBRIATUM 

GOLDERNROD 

GRAIN 

GRAMMA, BLUE 

GRASS, BERMUDA 

GRASS, BROME, CANARY, JOHNSON, JUNE, OAT, ORCHARD, QUACK 

GREASEWOOD 

GUM, BLACK, SWEET 

HACKBERRY 

HAY 

HAZELBERRY 

HAZELNUT, AMERICAN 

HELMINTHOSPORIUM SATIVUM 

HEMLOCK, WESTERN 

HEMP, COMMON 

HICKORY, MIXED, PIGNUS, SHELLBARK 

HISTOPLASMA, CAPSULATUM, FARCIMINOSUM 

HONEYSUCKLE 

HORMODENDRUM CLAD 

HOUSE 

IODINE BUSH 

IRIS VERSICOLOR 

JERUSALEM OAK 

JOHNSON GRASS SMUT 

JUNIPER 

LAMBSQUARTER 

LOMBARDY POPLAR 

MAGNOLIA 

142


MAPLE, SOFT, HARD 

MARIGOLD 

MARSHELDER, BURWEED, NARROWLEAF, ROUGH 

MEADOW FESCUE 

MESQUITE 

MEXICAN TEA 

MICROSPORUM, AUDOUINII, CANIS, GYPSEUM 

MONOTOSPORA 

MUCOR, CORYMBIFERA, MUCEDO, PLUMBEUS 

MUGWART, COMMON 

MULBERRY, PAPER, RED, WHITE 

MYCOGONE ALBA 

NARCISSUS 

NASTRUTIUM 

NEUROSPORA, SITOPHILA 

NIGROSPORA, SPHAERICA 

NOCARDIA ASTEROIDES 

OAK, BLACK, BLACKJACK, BUR, LIVE, POST, RED, WHITE 

OAKBLACK 

OAT, CULTIVATED 

PAEONIA OFFICINALIS 

PENICILLUM, CHRYSOGENUM, NOTATUM, RUBRUM 

PIGWEED 

PLANTAIN, ENGLISH 

POVERTY WEED 

QUAILBUSH 

RABBITBUSH 

RAGWEED, DESERT, FALSE, GIANT, SHORT, SLENDER, WESTERN 

WOOLY, MIX 

REDTOP 

RHIZOPUS NIGRICANS 

RHODOTORULA MUCILAGINOSA 

RINKEL 

ROSE 

RUSSIAN THISTLE 

RYE, CULTIVATED 

RYE GRASS, COMMON, ITALIAN, PERENNIAL 

SAFE, DRAGON, PASTURE, PRAIRIE, MIX 

SAGEBRUSH, COMMON 

SALTBUSH, ANNUAL 

SCOPULARIOPSIS 

SHADSCALE 

SHEEP SORREL 

SORGHUM, GRAIN 

143


SORGHUM, SMUT 

SPONDYLOCLANDIUM ATROVIRENS 

SPOROTRICHUM PRUINOSUM 

STACHYBOTRYS ATRA 

SUGAR BEET POLLEN 

SUNFLOWER 

SYNTHETIC FABRIC 

TOBACCO 

WEED POLLEN MIX 

WESTERN WATER HEMP 

WHEAT, CULTIVATED, GRASS 

WINGSCALE 

WINTERFAT 

WORMWOOD, ANNUAL, COMMON 

144

PHENOLS I 

ACC ACETALDEHYDE 

ACETIC ACID 

ACETONE 

ADENINE 

AFLATOXINS 

ALDEHYDE 

ALLYL BUTYRATE 

ALLYL TIGLATE 

AMSOLE 

AMYGDALIN 

ANETHOLE 

APIOL 

ARGININE 

ASPARAGINE 

d1-ALANINE 

BENZALDEHYDE 

BENZOIC ACID 

BENZOTHIAZOLE 

BENZYL 

BENZYL BUTYRATE 

BENZYL TIGLATE 

BHA 

BHT 

BIOFLAVENOIDS 

BRAIN SUBSTANCE 

BUTANOIC ACID 

BUTYRIC ACID 

d-BIOTIN 

CAFFEIC ACID 

CAFFEINE 

CALCIUM AMINO ACID CHELATE 

CALCIUM OROTATE 

CAMPHOR 

CANDIDA 

CAPSAICIN 

CAROTENE 

CARYOPHYLLENE 

CHALCONE 

CHLOROGENIC ACID 

CINEOL 

CINNAMALDEHYDE 

CINNAMIC ACID 

CONIFERYL ALCOHOL 

COUMARIN 

145

PHENOLS I, cont. 

DECANOIC ACID 

DOPAMINE 

ELLAGIO ACID 

EPHEDRINE HCL 

ESTERS (30 TYPES) 

ESTROGEN 

ETHYL BUTYRATE 

ETHYL HEPTANOATE 

ETHYL HEXANOATE 

ETHYL OCTANOATE 

EHTYL PROPIONATE 

ETHYL PYRUVATE 

ETHYL VALERATE 

EUGENOL 

FD&C BLUE NO. 1 

FD&C BLUE NO. 2 

FD&C GREEN NO. 3 

FD&C RED NO. 2 



FD&C VIOLET NO. 1 

FD&C YELLOW NO. 6 

FOLIC ACID 

FORMALDEHYDE DEHYDROGENASE 

FURFURAL 

FURFURYL BUTYRATE 

FURFURYL HEPTANOATE 

FURFURYL HEXANOATE 

FURFURYL OCTANOATE 

FURFURYL PENTANOATE 

FURFURYL PROPIONATE 

GABA 

GALLIC ACID 

GENISTEIN (BIOCHANIN A) 

GERMANIUM 

GLUTIN 

GLYCINE 

1-GLUTAMIC ACID 

HEART SUBSTANCE 

HEMOGLOBIN 

HESPERETIN 

HISTAMINE 

HYDROCINNAMIC ACID 

146


HYPOTHALAMUS SUBSTANCE 

n-HEXYL BUTYRATE 

n-HEXYL TIGLATE 

ICOLEUCINE 

INDOLE 

INOSINE 

INOSITOL 

ISOASCORBIC ACID 

ISOPROPYL BUTYRATE 

ISOPROPYL TIGLATE 

KIDNEY SUBSTANCE 

alpha-KETO GLUTARIC ACID 

L-CARNITINE HYDROCHLORIDE 

L-DOPA 

L-GLUTAMINE + GLUTAMIN ACID 

L-GLUTATHIONE 

L-LYSINE (PILL) 

LACTIC ACID 

LACTOSE 

LEUCINE 

LIMONEN 

LINALOOL 

LIPASE BLENDS 

LYMPHATIC SUBSTANCE 

MALIC ACID 

MALTOSE 

MALVIN 

MANGANESE AMINO ACID CHELATE 

MANNAN 

MENTHOL 

METHIONINE 

METHYL BUTYRATE 

METHYL SALICYLATE 

METHYL TIGLATE 

MINADIONE 

MOLYBDENUM AMINO ACID CHELATE 

MONO AMMONIUM GLYCYRRHIZINATE 

N, N-DIMETHYLGLYCINE HYDROCHLORIDE 

NARINGENIN 

NICOTINE 

NOREPINEPHRINE 

OCTACOSANOL 

OCTANOIC ACID 

OCTAPAMINE 

147


ORCHIC SUBSTANCE 

OVARIAN SUBSTANCE 

PABA 

PANCREATIN 

PANCRELIPASE 

PENTOSE 

PHENETHYL 2-METHYLBUTYRATE 

PHENYLALANINE 

PHENYLISOTHIO 

PHLORIDZIN 

PINENE 

148

ALLERSODES 

ACC 

Acetaldehyde 

Acetic Acid 

Acetone 

Adenine 

Aflatoxins 

dl-Alanine 

Aldehyde 

Allyl Butyrate 

Allyl Tiglate 

Amygdalin 

Anethole 

Apiol 

Arginine 

Asparagine 

Benzaldehyde 

Benzoic Acid 

Benzothiazole 

Benzyl 

Benzyl Butyrate 

Benzyl Tiglate 

BHA 

BHT (Buylated Hydroxytoluene) 

d-Biotin 

Bioflavenoids 

Brain Substance 

Butanoic Acid 

Butyric Acid 

Caffeic Acid 

Caffeine 

Calcium Chelate 

Camphor 

Candida 

Capsaicin 

Carotene 

L-Carnitine Hydrochloride 

Caryophyllene 

Chalcone 

Chlorogenic Acid 

Cineol 

Cinnamic Acid 

Coniferyl Alcohol 

Coumarin 

Decanoic Acid 

149

ALLERSODES, cont. 

N, N-Dimethylglycine Hydrochloride 

L-Dopa 

Dopamine 

Ellagic Acid 

Ephedrine HCl 

Esters (30 types) 

Estrogen 

Ethyl Butyrate 

Ethyl Heptanoate 

Ethyl Hexanoate 

Ethyl Octanoate 

Ethyl Propionate 

Ethyl Pyruvate 

Ethyl Valerate 

Eugenol 

FD&C Blue No. 1 

FD&C Blue No. 2 

FD&C Green No. 3 

FD&C Red No. 2 



FD&C Yellow No. 5 

FD&C Yellow No. 6 

FD&C Violet No. 1 

Folic Acid 

Formaldehyde 

Furfural 

Furfural Butyrate 

Furfural Heptanoate 

Furfural Hexanoate 

Furfural Octanoate 

Furfural Pentanoate 

Furfural Propionate 

GABA (Gamma-Amino Butyric Acid) 

Gallic Acid 

Genistein (Biochanin A) 

Germanium 

1-Glutamic Acid 

1-Glutamine 

L-Glutathione 

Glutin 

Glycine 

Glycyrrhizinate 

Heart Substance 

150


Hemoglobin 

Hesperetin 

Histamine 

Hydrocinnamic Acid 

Hypothalamus Substance 

Indole 

Inosine 

Inositol 

Isoascorbic Acid 

Isoleucine 

Isopropyl Butyrate 

Isopropyl Tiglate 

alpha-Keto Glutaric Acid 

Kidney Substance 

Lactic Acid 

Lactose 

Leucine 

Limonene 

Linalool 

Lipase Blends 

Lymphatic Substance 

Lysine 

Malic Acid 

Maltose 

Malvin 

Manganese Chelate 

Mannan 

Menadione 

Methionine 

Menthol 

Methyl Butyrate 

Methyl Salicylate 

Methyl Tiglate 

Molybdenum Chelate 

Naringenin 

Nicotine 

Norepinephrine 

Octacosanol 

Octanoic Acid 

Octopamine 

Orchic Substance 

Ovarian Substance 

PABA (Para Amino Benzoic Acid) 

Pancreatin 

151


Pancrelipase 

Pentose 

Phenethyl 2-Methylbutyrate 

Phenylalanine 

Phenylisothio 

Phloridzin 

Pinene 

Piperine 

Piperonal 

Pituitary Substance 

Progesterone 

Propyl Butyrate 

Propyl Tiglate 

Putresine 

Pyrrole 

Pyridoxal-5-Phosphate 

Pyridoxine Hydrochloride (Vitamin B-6) 

Phytic Acid 

Pyruvic 

Quercetin 

Red Bone Marrow 

Riboflavin (Vitamin B-2) 

Rutin 

Safrole 

Salsolinol 

Serotonin 

Skatol 

Spleen Substance 

Succinic Acid 

Suprarenal/Adrenal Substance 

Suprarenal Cortex 

Taurine 

Thiamine Hydrochloride (Vitamin B-1) 

Thujone 

Thymol 

Thymine 

Thyroid 

Trypsin 

Tryptophan 

Tyramine 

Tyrosine 

Ubiquinone 50 

Uric Acid 

Uterus Substance 

152


Valeraldehyde 

Vanillin 

d-Xylose 

153

ALLERGINS, ANTIGENS, FOODS 

Almond Meal 

Angora (Goat Mohair) 

Apple 

Banana 

Bean 

Birch Mix 

Brewers Yeast 

Broccoli 

Cabbage 

Carrot 

Cat 

Cattle 

Cauliflower 

Celery 

Cheese 

Cheddar Mix 

Chicken 

Chocolate 

Citrus 

Coffee 

Corn Pollen 

Cotton Seed 

Cotton Wood 

Cucumber 

Dock Sorrel 

Dog 

Dust Mix (House) 

Dust Mix (Mattress) 

Dust Mix (Rug) 

Dust Mix (Upholstery) 

Eastern Oak 

Egg White (Chicken) 

Elm Mix 

Feathers (Chicken, Goose, Duck) 

Flax Seed 

Flower Pollen I 

Fruit Juice 

Garlic 

Grain Mill Dust (Corn) 

Grain Mill Dust (Wheat) 

Grass (Alfalfa) 

Grass (Golden Rod) 

Grass (Kentucky Blue) 

Grass (Meadow Fescue) 

154

ALLERGINS, ANTIGENS, FOODS, cont. 

Grass (Orchard) 

Grass (Perennial Rye) 

Grass (Red Clover) 

Grass (Red Top) 

Grass (Sweet Vernal) 

Grass (Timothy) 

Green Pepper 

Hair Spray 

Hickory Mix 

Horse 

Juniper 

Kapok 

Kelp-Iodine 

Lemon 

Lettuce 

Maple Mix 

Milk 

Mold Mix 

Mulberry 

Mushroom 

Nut Mix (Almond) 

Nut Mix (Brazil) 

Nut Mix (Cashew) 

Nut Mix (Coconut) 

Nut Mix (English Walnut) 

Nut Mix (Peanut) 

Nut Mix (Pecan) 

Onion 

Orange 

Penicillium (Chrysogenum) 

Penicillium (Digitatum) 

Penicillium (Notatuer) 

Penicillium (Roquefort) 

Perfume Mix 

Pollen (Amaranthus) 

Pollen (Chenopodium) 

Pollen (Cockle Burr) 

Pollen (Daisy) 

Pollen (Dandelion) 

Pollen (Grass) 

Pollen (Honey Suckle) 

Pollen (Marsh Elder) 

Pollen (Mugwort) 

Pollen (White) 

155

ALLERGINS, ANTIGENS, FOODS, cont. 

Red Meat 

Rice 

Sage 

Salmon 

Scale Mix 

Sesame 

Sheep Wool 

Shellfish (Clam) 

Shellfish (Crab) 

Shellfish (Oyster) 

Shellfish (Scallop) 

Shellfish (Shrimp) 

Soybean 

Spinach 

Strawberry 

Tobacco 

Tomato 

Western Oak Mix 

156

THE DEHABITUATE PHILOSOPHY 

In our society today, addictions have become a dramatic problem in the 

culture’s disease structure. Many people have addictive tendencies and 

can become addicted to a variety of things, not just illegal drugs, but 

caffeine, tobacco, alcohol, sugar, sex, stress, and other things. 

The Dr. Recommends’ dehabituate remedies have been designed for 

homeopathic stimulation of the organism to deal with the addictions and 

discharge them in simple, natural ways. The dehabituate remedies have 

been engineered for safety through the QQC TM techniques. These 

remedies are only designed as an adjunct therapy to a more complete 

addiction reduction system. 

We recommend Alcoholics Anonymous, Gamblers Anonymous, or any 

other twelve-step programs that help people deal with these addictive 

tendencies. 

157

DEHABITUATE REMEDIES 

SMOKING DEHABITUATE 1 (1 fl. oz.) 


Indication: Systemic stimulation to help reduce smoking. Use during 

first 3 to 4 weeks as a nicotine supplement (Do not use beyond suggested 

dosage.) 

Ingredients: Nicotinum 3x. Calcarea Phosphorica, Zincum Metallicum 

4x. Lobelia cardinalis, Selenium Metallicum 6x. Bladder 6x, 12x, 30x, 

60x, 100x. Hypothalamus 6x, 12x, 30x, 60x, 100x. Lung 6x, 12x, 30x, 

60x, 100x. Beta-Endorphin 6x, 30x. Coffea Tosta 6x, 30x, 100x. Nux 

vomica 12x. Tabacum 12x, 16x, 24x, 100x. Saccharinum 16x, 100x. 

Plumbum Metallicum 18x 

SMOKING DEHABITUATE 2 (1 fl. oz.) 


Indication: Systemic stimulation to help reduce smoking. Use after first 

month as a detox and for relapse prevention. 

Ingredients: Zincum Metallicum, Calcarea Phosphorica 4x. Silicea, 

Lobelia inflata, Selenium Metallicum 6x. Sarcodes: Lung, 

Hypothalamus, Bladder 6x-12x, 30x, 60x, 100x. Endorphins 6x, 30x, 

100x, 500x, 1000x. Coffea 6x, 30x, 100x. Nux vomica 12x. Tabacum 

12x, 16x, 24x, 100x, 500x, 1000x. Saccharinum 16x, 50m. Plumbum 

Metallicum 18x, 100x, 1000x. Nicotinum 30x. 

158

VITAMINS 

The Dr. Recommends’ vitamin and mineral products can be used in a 

therapeutic practice. The sciences of nutritional medicine and 

orthomolecular biology have shown that compounds can be used to help 

patients in attaining balance. The science of nutritional deficiency and 

excess must be dealt with. 

The following products can be utilized to supplement patient’s diets, 

and also to help in orthomolecular ways through the stabilization of 

enzyme pathways, hormonal utilization, and vitamin integrity. These 

formulas are designed to work with the body naturally by assisting the 

nutritional intake of the patient and supplementing the needed vitamins 

and enzymes. 

159

LIQUID VITAMINS 

A-Z LIQUID (4 fl. oz.) 

Natural Source of Full-Range Essential Vitamins 

Ingredients: Aloe vera, Medicago sativa, Calcium Ascorbate, Panax 

quinquefolium 1x. Caryophyllus aromaticus, Ribes nigrum., Angelica 

archangelica 2x. Apis mellifica, Chromium, Selenium Metallicum 3x. 

In a tincture of water and non-allergenic alcohol. 

DRINKER'S VITAMIN (4 fl. oz.) 

Supplies Vitamins and Minerals depleted by alcohol 

Ingredients: Magnesium, Calcium Gluconate, B-Complex, Eggshell, 

Saccharomyces cerevisiae, Bee Pollen, Angelica archangelica 2x. Liver 

Sarcode, Tang Kuei, Oldenlandia affinis, Baptisia tinctoria, Prunus 

armeniaca 3x. In a tincture of water and non-allergenic alcohol. 

SMOKER'S VITAMIN (4 fl. oz.) 

Supplies Vitamins and Minerals depleted by smoking 

Ingredients: Ascorbic Acid, Beta Carotene 1x. Taraxacum officinale, 

Petroselinum sativum, Spinacia oleracea, Urtica dioica, Equisetum 

arvense 2x. Beta vulgaris, Paeonia officinalis, Carthamus tinctorius, 

Selenium Metallicum, Commiphora myrrha 3x. Ephedra sinica 4x. 

In a tincture of water and non-allergenic alcohol. 

HOMEOPATHIC CATALYST WATER (4 fl. oz.) 

Increases osmotic capacity 

NOTE: Should NOT be used by diabetics. 

Ingredients: Purified water, Non-allergenic alcohol, Chlorophyll, 

Magnesium, Stearic Acid, Natural Organic Tree Sap, Equisetum. 

160

VITAMINS 

ADERMINE HCL 

ANEURINE 

ANEURINE PYRO PHOSPHATE 

ARACDONIC ACID 

p-AMINOBENZOIC ACID 

BETA-CAROTENE 

BIOFLAVINOIDS 

CALCIFEROL 

CAPROIC ACID 

COENZYME Q6 

COENZYME Q7 

COENZYME Q8 

COENZYME Q9 

COENZYME Q10 

COLLAGEN 

CYTOCHROME 

CYTOCHROME FAD 

DESTHIOBIOTIN 

DICHLOROFOLIC ACID 

ELASTIN 

ERGO CALCIFEROL 

ERGOSTEROL 

FAD 

FERODOXIN 

GLUTATHIONE 

GSG GLUTATHIONE 

HYDROXO COBALAMINE 

LIBOAMIDE 

LINOLEIC ACID 

LINOLENIC ACID 

LIPOIC ACID 

NADP 

NAPATHO QUINONE 

NICOTINIC ACID 

ORTHO QUINONE 

PHYKO BIOTIN 

PORPHYRIN 

PTEROYLGLUTAMIC ACID 

PYCOCYANIN CYANIN 

RETINAL 

RETINOL 

RETINOL ACETATE 

RETINOL PALITATE 

THIOCTIC ACID 

161

TOCOPHEROL 

TRIGONELLINE 

UBIQUINONE –ALL 

UBIQUINONE -30 

UBIQUINONE-35 

UBIQUINONE-40 

UBIQUINONE-45 

UBIQUINONE-50 

VITAMIN A 

VITAMIN A2 

VITAMIN A3 

VITAMIN B1 

VITAMIN B2 

VITAMIN B3 

VITAMIN B4 

VITAMIN B5 

VITAMIN B6 

VITAMIN B7 

VITAMIN B 8 

VITAMIN B9 

VITAMIN B10 

VITAMIN B11 

VITAMIN B12 

VITAMIN B13 

VITAMIN B14 

VITAMIN B15 

VITAMIN B16 

VITAMIN B17 

VITAMIN B18 

VITAMIN B19 

VITAMIN B20 

VITAMIN C 

VITAMIN D 

VITAMIN D2 

VITAMIN D3 

VITAMIN E 

VITAMIN F-ALL 

VITAMIN K 

VITAMIN U 

162

POWDERED PRODUCTS 

In keeping with the Dr. Recommends’ philosophy which involves 

digestion starting in the mouth, there are various powdered products 

available that contain different minerals, vitamins, enzymes and other 

ingredients that are not easily made into liquids. They have long shelf 

lives in powdered form, and can be utilized by patients for detoxification 

and other things for long periods of time, safely and efficiently. 

Many of the powders can be stirred into juices or other liquids by the 

patient and taken as part of his/her daily regime. These must be used 

with the help of a trained practitioner or skilled professional to help the 

patient in treatment. 

POWDERS 

ACTIVATED CHARCOAL POWDER (6 oz.) 

Ingredients: Activated Charcoal Powder. 

ANTACID POWDER (6 oz.) 

Ingredients: Kali Bicarbonate, Natrum Bicarbonate, Calcium Carbonate, 

Magnesium Phosphorica, Natrum Muraticum, Kali Muraticum, Silicea. 

CLEANSING & SKIN POULTICE (6 oz.) 

Applied to skin to draw out toxins, Intestinal Cleanse 

Ingredients: Organic Bentonite, Activated Charcoal, Orsa Clay, 

Equisetum arvense, Symphytum officinale, Arnica montana, Myristica 

fragrans, Magnesia Sulphurica, Natrum Muriaticum, Capsicum annuum. 

DISODIUM PHOSPHATE POWDER (6 oz.) 

Ingredients: Disodium Phosphate, Magnesia Sulphurica. 

MUSTARD POULTICE (6 oz.) 

Ingredients: Bentonite, Brassica nigra, Brassica alba, Sanguinaria 

Canadensis, Symphytum officinale, Urtica dioica, Arctium lappa, Carica 

papaya, Activated Charcoal, Capsicum frutescens. 

163

Screening Groups Used in the Academy of Applied Quantum 

Biotech Computer Programs 

Listed here are some screening groups used in the Academy of 

Applied Quantum Biotech computer programs with biofeedback 

instrumentation for bio-computer analysis. These compounds can be 

used and purchased as homeopathics. 

THE SCREENING GROUPS 

Congenital 1 Syphilinum 

Syphlitic miasm 

Medorrhinum 

Gonococcinum 

Papilloma Virus 

Congenital 2 Tuberculinum Kock 

Tuberculinum Bovinum 

Tuberculinum Avis 

Bacillinum 

Retrovirus 

Congenital 3 Tuberculinum Klebs 

Tuberculinum Denys 

Tuberculinum Rosen 

Tuberculinum 

Marmoret 

Ricketsia 

Upper Respiratory Bacteria 1 Staphlococcus Aureus 

Strept B haemolyticus 

Pneumococcus 

Haemophilus influenza 

Tersina Pestis 

164

Bowel Nosodes 1 E. Coli 

Proteus 

Pseudomonas (Bac. 

pyocyanus) 

Klebsiella pneumoniae 

Thermal Baccilli 

Bowel Nosodes 2 Staph abdominalis 

Strept faecalis 

Enterococcus 

Bacteroides 

Pseudomonas 

Bowel Nosodes 3 Typhiodinum sp. 

Shigella dysenteriae 

Cholera 

Pasturella 

Giardia 

Bowel Nosodes 4 Tularemia 

Clostridium welchii 

Shigella sonnei 

Bowel Nosodes 5 Acidophilous 

Bifidus 

Bulgaricus 

Caucaucous 

Lacto Baccilus (All) 

Upper Respiratory Viruses Adenovirus 

Rhinovirus 

Coronavirus 

Respiratory syncytial 

virus 

Retro Virus HLV 1-2 

HLV 3-4-5 

HLV 6-7-8 

HLV 9-10-11-12 

ARC 

165

Influenzal Screen Influenza, all 

varieties 

Influenza A 

Influenza B 

Influenza current 

year (79/80) 

Enteric Viruses Retrovirus 

Polio 

Coxackie 

Echo virus 

Liver Viruses Hepatitis A 

Hepatitis B 

Hepatitis C 

Cytomegalovirus 

Epstein-Barr virus 

Childhood Viruses Parotidinum 

Rubella 

Morbillinum 

Roseola infantum 

Herpes (All) 

Protozoal Screen Malaria 

Toxoplasmosis 

Entamoeba histolytica 

Strongaloides 

Amoeba (All) 

Fungal Screen #1 Tines 

Aspergillus 

Coccidiomycosis 

Histoplasmosis 

Blasto Hominus 

(Mycosis) 

Fungal Screen #2 Cryptococcus 

Aspergillus 

Sacromyces 

Mycosis 

Tycosporon 

166

Fungal Screen #3 Candida Albicans 

Candida Rugosa 

Candida Stellerata 

Candida Tropicalis 

Candida Krusei 

Venereal Group Syphilinum 

Medorrhinum 

Chlamydia 

trachomitis 

Mycoplasma (All) 

Papiloma 

Uric Acid Metabolic Group Acid uricum 

Hypoxanthine 

Kreatine 

Glutamine 

Oxalic Acidum 

Lipid Group Screen Cholesterinum 

Blycerinum 

Acid acetessigsour- 

aethylester (acetic 

acid ethylester) 

Acetone 

Triglyceridus 

Liver Miscellaneous Brucella abortus 

Listeria monocytogenes 

Leptospirosis 

Tularemia 

Glandular Fever 

Urinary Tract Irritants Acid citricum 

Acid sorbicum 

Acid benzoicum 

Terebinthina 

Allergic Irritant 

167

Nephrolithiasis Screen Acid oxalicum 

Acid uricum 

Calcarea 

phosphoricum 

Calcarea sulfuricum 

Acid Nitricum 

(Proteins) 

Vaginitis Screen Candida albicans 

Trichomonus 

vaginalis 

Haemophilus 

vaginalis 

Strep faecalis 

Allergic Vaginitis 

Accessory Lung Pathogens Chlamydia 

psittacosis 

Mycopolasma 

pneumoniae 

Parainfluenza viruses 

Actinomycosis Israeli 

Crypto Cystitis 

Aspergillus 

Histoplasmosis 

Respiratory Tract Irritants Tobacco smoke 

Auto exhaust fumes 

Acid sulfurous 

Asbestos 

Allergic Irritant 

Stimulant Screen #1 Coffee cruda 

Tobacco smoke 

Caffeine 

Tea (Thea Chinese) 

Sugar 

168

Stimulant Screen #2 Salt 

Animal fat 

Theo-bromine 

Adrenal stress protein 

Salicylate Screen Acid salicylicum 

Acid acetyl salicylicum 

Food dyes 

Sodium bisulfide 

Heavy Metals 1 Arsenicum album 

Plumbum metallicum 

Cadmium met. 

Merc. sol. 

Molybdenum 

Heavy Metals 2 Stannum met. 

Aluminum 

Cuprum metallicum 

(copper) 

Niccolum metallicum 

(nickel) 

Antimony 

Heavy Metals #3 Barium 

Germanium 

Gold 

Vanadium 

Silver 

Heavy Metals #4 Plutonium 

(Radioactive) Uranium 

Radium 

Radon 

Cesium 

Parasite Screen #1 Giardia lambia 

Enterobius 

vermicularis 

Ascaris lumbriocoides 

Oxyures vermicularis 

Blastohominus 

169

Parasite Screen #2 Ancylostoma 

Chilomastix 

Diphylidium 

Endolimax 

Necator Americanus 

Parasite Screen #3 Fasciola hepatica 

Dicrocdelium 

lanceatum 

Hymenocepis 

Schistosoma 

Teania 

Nerual Viruses Vaccininum 

Variolinum 

Varicella 

Herpes zoster 

Meningitis (Viral) 

Neurotoxins 1 Tetanus 

Botulinum 

Q-fever 

Scarlatinum 

Salmonella 

Neurotoxins 2 Hydrophobinum 

Distemperinum 

Arbovirus 

Tick fever 

Candida Albicanus 

Herpes Group Herpes Simplex I 

Herpes Simplex II 

Herpes Simplex 

Herpes Progenitalis 

Herpes Zoster 

Adrenal Screen Diptherinum 

Toxoplasmosis 

Tularemia 

Meningecoccinum 

Pseudomonas 

170

Food Additive Screen Acid salycylicum 

Butylated 

hydroxyanasol 

Sodium nitrate 

Monosodium glutamate 

Synthetic Chemicals 

Addex 

Dermatology Irritants Rhus tox 

Niccolum metallicum 

Petroleum 

Benzoin 

Hydro carbons (All) 

Toxic Bowel Metabolites Indol 

Skatol 

Mercaptan 

Thioether 

Sulphur 

Antibiotic Screen Penicillin 

Erythromycin 

Tetracycline 

Sulfanilimide 

Chemex 

Synthetic Chemicals 

Epidermals House dust 

House dust mite 

Cat/Dog hair 

Feathers 

House dust scale 

Pollen Mix Grass mix 1, 2, 3 

Tree mix 

Weed mix 

Flower Pollen 

Grains 

Mold Spore Mix Mold mix A 

Mold mix B 

T.O.E. 

Candida albicans 

FNG 

Fungifuge 

171

Phenol Group Acid carbolicum 

Acid benzoicum 

Creosole 

Kreosotum 

Phenols (All) 

Hydrocarbon Group Ethyl alcohol 

Petroleum 

Kerosene 

Diesel 

Envrox, Enviro. 

Industrial Pollutants 

Miscellaneous Chemicals Formaldehyde 

Acetone 

Acid sulfurosum 

Benzenium 

Industriox 

Industrial pollutants 

Mutagen/Carcinogen Group Methylcholanthrene 

Nitrosamine 

Benzene 

Chloroform 

Phosphorous 

compounds 

Pesticides 1 – Halogenated Hydrocarbons D.D.T. 

Lindane 

Hexachlorbenzol 

Heptachlor 

Insecticides 

Pesticide 2 – Organophosphates Malathion 

Parathion 

DDVP 

Diazanon 

Addex 

Insecticides 

Pesticide 3 – Carbamates Dithiocarbamate 

Aldicarb 

172

Pesticide 4 – Miscellaneous Paraquat 

2, 4, 5, t-Ester 

Dinitrokresol 

Diquat 

Dental Materials 1 Chrom Cobart 

Molybdenum 

Gold 

Silver amalgam 

Palladium 

Amalgam 

Dental Materials 

Dental Materials 2 Phosphate cement 

Carboxylate cement 

Polymerisat 

Zinc oxydatum 

Phenol/Cresol 

Gingival Screen Gingivitis 

Ulcer gingivitis 

Necrotic gingivitis 

Amoebic gingivitis 

Periodontal Screen Zahnfleistasche 

Paradontose 

Zahnsacken 

Periodontitis 

Parulis (Strep muc.) 

Parulis (Staph aur.) 

Pulpitis Screen Gangranose pulpa 

Acute pulpitis 

Chronic pulpitis 

Toxic pulpitis 

Periapical Screen Odonton Fudus 

Root canal granuloma 

Gangran granuloma 

Radicular cyste 

173

Jaw Lesion Screen Jaw ostitis 

Exudative ostitis 

Acute bacterial ostitis 

Chronic bacteria ostitis 

Infective ostitis 

Injury ostitis 

Foci Screen #1 Foci in right lower jaw 

Foci in left lower jaw 

Foci in right upper jaw 

Foci in left upper jaw 

Foci in cranium 

Foci Screen #2 Foci in cranial vertebrae 

Foci in cervical 

vertebrae 

Foci in thoracic 

vertebrae 

Foci in lumbar 

vertebrae 

Foci in sacral vertebrae 

Foci Screen #3 Foci in palatine tonsils 

Foci in adenoids 

Foci in pharyngeal 

tonsils 

Foci in tubal tonsil 

Foci in laryngeal tonsil 

Foci Screen #4 Foci in maxillary sinus 

Foci in cavernous sinus 

Foci in sphenoidal sinus 

Foci in ethmoid cell 

Foci in frontal sinus 

Foci Screen #5 Lesions in body 

Foci in head area 

Foci in right upper 

quadrant 

Foci in left upper 

quadrant 

Foci in right lower 

quadrant 

Foci in left lower 

quadrant 

174

Foci Screen #6 Right side brain 

Foci in frontal lobe 

Foci in temporal lobe 

Foci in parietal lobe 

Foci in occipital lobe 

Foci in midbrain 

Foci Screen #7 Left side brain 

Foci in frontal lobe 

Foci in temporal lobe 

Foci in parietal lobe 

Foci in occipital lobe 

Foci in midbrain 

Foci Screen #8 Neurological 

Foci in (Ans) para- 

sympathetic nerves 

Foci in (Ans) 

sympathetic nerves 

Foci in (Cns) motor 

nerves 

Foci in (Cns) sensory 

nerves 

Foci in cranial nerves 

Foci Screen #9 Digestive dist. 

Foci in stomach 

Foci in small intestine 

Foci in large intestine 

Foci in liver 

Foci in pancreas 

175

INDICATED SCREENING GROUPS 

FOR THE MERIDIANS AND VESSELS OF ELECTROACUPUNCTURE 

ACCORDING TO DR. REINHOLD VOLL 

SPLEEN 

Sp4 Congenital 1, 2, 3 

Liver viruses 

Enteric viruses 

Protozoan group 

Heavy metals 1, 2 

Sp3 Hepatitis viruses 


Dental materials 


PANCREAS 

Pn1 Hepatitis viruses 


Childhood viral 

illnesses 

Toxic bowel 

metabolites 

Bowel nosodes 1-4 

Pn2 Upper respiratory 

bacteria 1 

Uric acid metabolite 

group 

Pn3 Childhood viruses 

Hepatitis viruses 



Pn4 Lipid metabolic group 


Childhood viruses 

176

STOMACH Congenital 1, 2, 3 

Upper respiratory 

bacteria 1 



Dental materials 1 

LIVER Liver viruses 


Congenital 1, 2, 3 

Protozoal group 


Liver miscellaneous 

Fungal group 

Insecticide groups 

Salicylate combo 

Common antibiotics 

Stimulant screen 

GALL BLADDER Bowel nosodes 1-4 

Lipid metabolite group 


Intestinal parasites 

KIDNEY 

Ki1 & Ki2 Bowel nosodes 1, 2 

Nephrolithiasis group 

Urinary tract irritants 


Ki2a & Ki3 U.R.I. bacteria 1, 2 



Food testing 

Common stimulant 

group 

177

UROGENITAL 

B1 67 Bowel nosodes 1, 2 


Venereal screen 


B1 65, 64 (male) Congenital 1, 2, 3 



Vaginitis group 

Bowel group 1, 2 

B1 65, 64 (female) Congenital 1, 2, 3 



Vaginitis group 

Bowel group 1, 2 

LUNG Congenital 1, 2, 3 

U.R.I. bacteria 1, 2 

U.R.I. viruses 

Influenzal group 

Bowel nosodes 1, 2 


Accessory lung 

pathogens 

Respiratory tract 

irritants 

Salicylate screen 

Fungus screen 

LARYNX/HYPOPHARYNX Use above nosode 

screen as for Lung 

LARGE INTESTINE Parasite screen 

Protozoan screen 




Liver viruses 

Mutagen/Carcinogen 

screen 


Toxic bowel 

metabolites 

178

SMALL INTESTINE Congenital nosodes 

1, 2, 3 



Liver viruses 


Parasite screen 

Protozoal screen 

HEART Congenital 1, 2, 3 

Influenzal screen 


Liver viruses 


viruses 


bacteria 1, 2 


Neurotoxin screen 

Neural viruses 

Herpes group 


Common stimulants 

Insecticide screen 


NERVOUS SYSTEM Congenital1, 2, 3 

Neural viruses 

Neurotoxins screen 




Liver viruses 



viruses 


Insecticides 

179

MENINGES 

ND 1b Congenital 1, 2, 3 


viruses 


bacteria 1, 2 



ND 1a Basic autonomic 

screening protocol 

Hydrocarbon group 

Phenol group 

Miscellaneous group 

Food additive group 

Stimulant group 

Antibiotic group 

Respiratory irritant 

group 

Toxic bowel 

metabolites 

Dental materials 1, 2 

Root canal group 

Heavy metal group 1, 2 

Pesticide group 1-4 

plus all nosode 

groups for 

Nervous System 

groups 

CIRCULATION Congenital 1, 2, 3 


bacteria 2 


Liver viruses 


Dental materials 

Mutagen/Carcinogen 

screen 

Neurotoxins 1, 2 

180

ENDOCRINE - Triple Warmer Meridian 

Tw1 (adrenal) Congenital 1, 2, 3 

Tw1 (gonads) Adrenal screen 

Refer to nosodes B1 65, 

64 for male and female 

Tw2 (Thyroid) Congenital 1, 2, 3 

(Parathyroid) Upper respiratory 

(Thymus) viruses 



bacteria 1, 2 



Tw3 (Pituitary) Congenital 1, 2, 3 

(Pineal) Upper respiratory 

viruses 





ALLERGY VESSEL 

Allergy 1 Food screens 


Insecticide screens 

Food additive screen 

Dermatology 

irritants 


Parasite screen 

ADG 1a Basic autonomic 

screening protocol 



ADG 2 Pollen screen 

Mold screen 

Epidermal screen 

Food screening 

181

ADG 3 Pollen screen 

Mold screen 

Epidermal screen 

Insect stings 


SKIN Congenital 1, 2 



bacteria 1, 2 

Refer to pancreas 

Refer to liver 

Dermatology irritant 

screen 

Mold screen 

Food screens 



Toxic bowel metabolites 

JOINT DEGENERATION & Congenital 1, 2, 3 

FIBROID DEGENERATION Upper respiratory 

(Connective Tissue) bacteria 1, 2 


Liver viruses 


Dental pure culture 

nosodes 

LYMPHATIC VESSEL Congenital 1, 2, 3 

Lyl, Lyl-La, Lyla (Tonsils, Pharynx, Middle Ear) viruses 


bacteria 1, 2 




nosodes 

Bowel nosodes 1 

182

Ly3 (Nose and Paranasal Sinuses) Congenital 1, 2, 3 

U. R. I. viruses 

U. R. I. bacteria 1, 2 

Influenza screen 

Bowel nosode group 1 

Remember to refer to 

ADG 3, ND3a & Twla 

Ly2a (Eyes) Congenital 1, 2, 3 

U. R. I. viruses 

U. R. I. bacteria 1, 2 




Fungal screen 

Ly2 (Dental) Dental materials 1, 2 

Root canal screen 

Gingival screen 

Pulpitis screen 

Periodontal screen 

(remember Tw2) 

Periapical screen 


bacteria 1 


nosodes 


Jaw lesion screen 

183

AN OPERANT DEFINITION OF HOMEOPATHY 

Homeopathy has been cloaked in mystery and misunderstanding, in 

that there are many principles which have not fully done justice to the 

complete range of homeopathic action. Many proponents use 

homeopathy in vastly different ways making the field look confused and 

irregular. 

One of the misconceptions is that it is assumed that all things are 

reversal in homeopathy that what a substance causes in a large dose it 

will reverse in a minute dose. This is not always so, and we will dedicate 

this chapter to that topic. 

As is pointed out in the chapter on snake venoms, the Arndt-Schultz 

law allows for the principle that what a poison might do at a raw dose, an 

extreme dilution of that poison will often time produce a paradoxical 

reversal of activity. If a patient were having a heart arrhythmia or 

irregularity, rattle snake venom, which causes a proteolytic effect on 

tissues and also has a cardio toxic effect on the heart muscles, 

oftentimes in small quantities, can help reverse the arrhythmia and 

stabilize the heart. The chapter on venoms and poison goes into this in 

detail. 

Dr. James P. Isaacs, in his book entitled Complementarity in Biology: 

Quantization of Molecular Motion. (James P. Isaacs, John C. Lamb: John 

Hopkins Press: Baltimore, 1969), points out another law of pharmacology 

which is Wilder’s law of initial value. In Wilder’s law, if a substance is not 

a poison, as we make it more and more dilute, one of three things will 

happen: 1) it still could have a reversal, 2) there might be an increase in 

the original effect, or 3) nothing may happen at all. This is Wilder’s law of 

initial value. It is often used in pharmacology to chart out dose response 

curves. 

Many herbals, plants, glandulars, minerals, etc., are used in 

homeopathy and are not poisonous. Some of these will not always have 

184

eversal effects. A classic example often noted in the literature is that of 

Eyebright. Eyebright is an herb used in homeopathy and herbal 

remedies. The name was coined because of the product’s positive effect 

on vision and the optic system. It helps make eyes bright. That is the 

herbal indication for Eyebright. The homeopathic indication for it is 

exactly the same. It is also used for vision problems, and to help patients 

with optical disturbances. If everything in homeopathy were truly all 

reversal, we would only use Eyebright on the patients who had vision 

that was too perfect, because then the reversal effect of Eyebright in 

homeopathic form would be that it would interfere with vision. This is 

not the case. 

It is also not the case in many types of sarcodal formulas. Thyroid 

tissue has been demonstrated to have positive effects on the thyroid 

system, and the thyroid hormone from the tissue can be utilized in cases 

of hypothyroidism to stabilize thyroid function. In homeopathic form this 

same thyroid tissue, as a sarcode, has the exact same indications. It can 

also be utilized in the hypothyroid condition in which the patient has a 

weak thyroid gland. 

Examples of sarcodal remedies abound in this non-reversal action. 

Adrenaline tissue, brain tissue, endocrine systems, heart tissue and the 

like, all have the same indications homeopathically as they do in 

glandular technology when used in raw dose. In all of these cases the 

glandulars (sarcodes) are used to stabilize function. Thus, they can be 

used in hyper or hypo cases. In the case of hyperthyroidism or 

hypothyroidism, the thyroid sarcode might be used which helps stabilize 

tissue. But it is not always reversal. 

The sarcodal remedies, as we proved in the chapter on sarcodes, will 

have a stabilizing effect in rejuvenating or increasing the probability that 

healthy tissues will ensue in the organism. As the organism produces 

new tissues in the thyroid, the cervical, the vertebrae, or wherever in the 

body, the homeopathic sarcodal therapy can help to insure that healthy 

185

tissues will be built instead of unhealthy ones. The sarcodal forms of 

homeopathics do not follow what is thought about homeopathy; that it is 

all reversal of action. 

Another example in homeopathy is the indications of calendula. 

Calendula, which is taken from the marigold plant, has been used by 

herbalists for centuries, if not eons, for different injuries. The 

homeopathic indications for calendula are equivalent. Oftentimes 

homeopaths will find that the dilute form of calendula can, in certain 

cases, have increased activity in treatment of injuries, and trauma 

conditions. 

James Tyler Kent writes that homeopathic calendula cannot be denied 

its ability to help in accident or injury cases. Another example is 

Dioscoria villosa, known as wild yam. The herbal therapeutics of it is that 

it is hepatic, stomachic, atonic, expectorant, anti-spasmodic, a sedative, 

and an anti-asthmatic. Its herbal uses include colic, jaundice, 

hardening/blocking of the liver, nausea (in pregnant women), cholera, 

neuralgia, hiccups, whooping cough, bronchitis, etc. Homeopathic 

indications are for painful afflictions of the abdomen, pelvic viscera, 

feeble digestive powers, colic, gallstones, heart spasms, uterine colic, 

back pain, and cramps. There are almost identical indications for the 

homeopathic as for the herbal. 

We now look at the herb Caulophyllum also known as squawroot or 

blue cohosh. It is used as an anti-spasmodic, nervine tonic, diuretic, 

anti-rheumatic, and anti-inflammatory. It is known as “woman’s best 

friend” for the reason that it has a powerful effect on stabilizing women’s 

systems, and helping in the alleviation of cramps. This remedy is 

excellent for spasms, epilepsy, uterine inflammation, and the like. If 

everything worked in reversal, we would use the cohosh for the opposite 

indications of its herbal. 

186

Let us now look at the homeopathic indications. Oscar E. Boericke’s 

repertory calls it Caulophyllum, and it is a woman’s remedy. During 

labor, when pains are present, the patient is exhausted and fretful. This 

remedy is excellent in its ability to help birthing pains. It is good for the 

stomach, dyspepsia, and all problems of the female system. It increases 

stability of menses and leucorrhea, and works for stiff joints, etc. Here is 

another example that the herbal recommendations are the same as the 

homeopathic. Even using this in dramatically dilute form, at 30x, and 

40x, there is stability in its action. 

Another example is Blue Vervain, in Latin; Verbena. Its herbal 

indications are that of a nervine tonic, anti-spasmodic, diaphoretic, and 

beneficial for the stomach; astringent, fever-fugue, and antiseptic. Its 

uses are for dyspepsia, indigestion, all liver conditions, kidney/bladder 

complaints, amenorrhea, dysmenorrhea, hysteria, epilepsy, chorea, 

nervous exhaustion, insomnia, diarrhea, nervous system, nervous 

depression, weakness, spasms, and irritation. It promotes the absorption 

of blood, and helps in pain and bruises. It is tremendously helpful for the 

liver, insomnia, epilepsy, hallucinations, and mental exhaustion. Find 

below a list of some of the formulas in the HPUS (Homeopathic 

Pharmacopeia of the United States) which have similar indications 

herbally as well as homeopathically. 

As we go through the HPUS we will see that 65% or more of the HPUS 

has similar indications herbally and homeopathically, making the two 

modalities almost equal. By building this new definition into homeopathy 

we can utilize the best of homeopathy, as well as naturopathy and herbal 

therapy to help the American public demystify some of the homeopathic 

reactions. This will give needed publicity as well as simplicity to allow 

them to choose the system of homeopathy as a medical modality. 

As can be seen from the dose-response curve in Figures 1, 2, and 3, 

there are dramatic differences between the Arndt-Schultz principle of 

poisons and Wilder’s law of initial value. 

187

LIST OF HOMEOPATHIC REMEDIES WITH SIMILAR HERBAL ACTION 

Abelmoschus Aquilegi 

Abies Nigra Aquilegia Vulgaris 

Abrotanum Aralia Dispida 

Achyranthes Calea Aralia Quinquefolia 

Actae Spicata Arbutus Andrach 

Adamas Areca Catechu 

Adelheidsquelle Artemisia Vulgaris 

Adonis Virnalis Arum Dracontium 

Adrenaline Arum Italicum 

Aesculus Glabra Arum Maculatum 

Aesculus Hippocastanum Arum Triphyllum 

Agave Americana Arundo Mauritanica 

Agave Tequilana Asclepias Incarnata 

Agnus Castus Asclepias Syriaca 

Agrimonia Eupatoria Asimina Triloba 

Agrostemma Githago Asparagus Officin 

Aletris Farinosa Aspidosperma 

Alfalfa Asperula Odorata 

Alisma Plantago Avena Sativa 

Allium Sativum Barosma 

Alnus Glutinosa Bellis Perennis 

Aloe Socotrina Berberis Aquifolium 

Alstonia Constricta Berberis Vulgaris 

Alstonia Scholaris Berberis Vulgaris, Fructus 

Althaea Officinalis Beta Vulgaris 

Ammi Visnaga Bixa Orellana 

Ampelopsis Quinquefolia Boldo 

Amygdalus Persica Borago Officinalis 

Anagallis Arvensis Branca Ursina 

Ananassa Brassica Napus 

Anchusa Officinalis Buxus Sempervirens 

Anemone Nemorosa Cacao 

Anemopsis California Cactus Grande 

Anethum Graveolens Cahinca 

Angelica Archangelica Cajuputum 

Angelica Atropurpurea Calcarea Acetica 

Angophora Lanceolata Calcarea Lactica 

Anthenis Nobilis Calendula Officinalis 

Apium Graveolens Calotropis Gigantea 

Apocynum Andro Calthapalustris 

Aqua Marina Canlophylum 

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Canchalagua Clematis Vitalba, Folia 

Canna Anjustifolia Coccus Cacti 

Carduus Benedictus Cochlearia Armoracia 

Carduus Marianus Cochlearia Officinalis 

Carum Carvi Collinsonia Canadensis 

Cascara Comocladia Dentata 

Cascarilla Conchiolinum 

Castanea Vesca Condurango 

Castoreum Convolvulus Arvensis 

Catalpa Bignonioides Copaiva Officinalis 

Cataria Nepeta Cornus Alternifolia 

Ceanothus Cornus Circinata 

Ceanothus Americanus Cornus Florida 

Cedron Crocus Sativa 

Celtis Occidentalis Crataegus 

Cephalanthus Occidentalis Cucurbita Citrullus 

Cerasus Virginiana Cucurbita Pepo, Flos 

Cereus Bonplandii Cucurbita Pepo, Semen 

Cereus Serpentinus Cuphea petiolata 

Cetraria Islandica Cydonia Vulgaris 

Chamomilla Cynara Scolymus 

Cheiranthus Cheiri Cypripedium Pubescens 

Chelidonium Majus Cytisus Scoparius 

Chelidonium Majus, Radix Daphne Indica 

Chelone Glabra Dictamnus Albus 

Chenopodium Anthelminticum Dioscorea Villosa 

Chenopodim Vulvaria Dirca Palustris 

Chimaphila Maculata Dolichos Pruriens 

Chimaphila Umbellata Draba Verna 

Chionanthus Virginica Drosera Rotundifolia 

Chrysanthemum Leucanthemum Dulcamara, Flos 

Cicer Arietinum Echinacea Angustifolia 

Cichorium Intybus Elaeis Guineensis 

Cimicifuga Racemosa Elaterium 

Cineraria Maritima Epiiedra Vulgaris 

Cinnamomum Epigaea Repens 

Cistus Canadensis Epilobium Palustre 

Citrus Decumana Epiphegus Virginiana 

Citrus Limonum Equisetum Arvense 

Citrus Vulgaris Erechtites Hieracifolia 

Clematis Virginiana Erigeron Canadensis 

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Eriodictyon Californicum Glycerinum 

Erodium Glycogenum 

Eryngium Aquaticum Glycyrrhiza Glabra 

Eryngium Maritimum Gnaphalium Leontopodium 

Erythraea Centaurium Gossypium Herbaceum 

Ethylicum Granatum 

Eugenia Caryophyllata Gratiola Officinalis 

Eugenia Jambosa Grindelia 

Euonymus Atropurpureus Guaco 

Euonymus Europaeus Guaiacum 

Eupatorium Aromaticum Guatteria Gaumeri 

Eupatorium Cannabinum Gymnocladus Canadensis 

Eupatorium Perfoliatum Haematoxylon Campechianum 

Eupatorium Purpureum Hamamelis Virginiana 

Euphrasia Officinalis Haronga Madagascariensis 

Fagopyrum Esculentum Helianthus Annuus 

Fagus Sylvatica Heliotropium Peruvianum 

Ferula Glauca Helonias Dioica 

Ficus Religiosa Hedeoma 

Filix Mas Helleborus 

Foeniculum Vulgare Hepatica Triloba 

Fragaria Vesca Hoang-Nan 

Franciscea Uniflora Homarus 

Fraxinus Americana Hura Crepitans 

Fraxinus Excelsior Hydrangea Arborescens 

Fucus Vesiculosus Hydrastis 

Galanthus Nivalis Hydrastis Canadensis 

Galega Officinalis Hydrocotyle 

Galium Aparine Hydrocotyle Asiatica 

Galphimia Glauca Hydrophyllum Virginianum 

Gambogia Hypericum 

Gaultheria Procumbens Iberis Amara 

Genista Tinctoria Ilex Aquifolium 

Gentiana Lutea Ilex Paraguariensis 

Gentiana Quinquefolia Illicium Anisatum 

Geranium Maculatum Imperatoria Ostruthium 

Geranium Robertianum Inula Helenium 

Geum Rivale Iris Florentina 

Geum Urbanum Iris Foetidissima 

Ginkgo Biloba Iris Germanica 

Glechoma Hederacea Iris Tenax 

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Iris Versicolor Magnesia Grandiflora 

Jacaranda Caroba Mandragora Officinarum 

Jalapa Mangifera Indica 

Juglans Cinerea Marrubium Bulgare 

Juniperus Communis Matica 

Juniperus Virginiana Melissa Officinalis 

Justicia Adhatoda Menispermum Canadense 

Kamala Mentha Piperita 

Karaka Mentha Pulegium 

Kousso Mentha Viridis 

Laburnum Anagyroides Mentholum 

Lacerta Agilis Menyanthes Trifoliata 

Lachnanthes Tinctoria Mezereum 

Lamium Album Millefolium 

Lappa Major Mimosa Humilis 

Lathyrus Sativus Mitchella Repens 

Lecithin Momordica Balsamina 

Lemna Minor Musa Sapientum 

Leonurus Cardiaca Myosotis 

Lepidium Bonariense Myrica Cerifera 

Leptandra Virginica Myristica Sebifera 

Lespedeza Captiata Myrrha 

Levisticum Officinale Myrtus Communis 

Liatris Spicata Nabalus Serpentarius 

Lilium Tigrinum Narcissus Pseudo-Narcissus 

Linaria Vulgaris Nasturtium Aquaticum 

Linum Usitatissimum Negundo 

Lonicera Periclymenum Nepeta Cataria 

Lonicera Xylosteum Nux Moschata 

Lophophytum Leandri Nymphaea Odorata 

Luffa Operculata Ocimum Basilicum 

Lupulinum Ocimum Canum 

Lycopersicum Esculentum Oenothera Biennis 

Lycopodium Clavatum Oleander 

Lycopus Virginicus Oleum Carvi 

Lysimachia Nummularia Ononis Spinosa 

Macrotinum Onopurdum 

Magnesia Carbonica Opuntia Vulgaris 

Magnesia Muriatica Oreodaphne 

Magnesia Oxydata Origanum Majorana 

Magnesia Sulfurica Ornithogalum Umbellatum 

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Ostrya Primula Vulgaris 

Ovi Gallinae Pellicula Prunus Padus 

Oxalis Acetosella Prunus Spinosa 

Oxydendrum Arboreum Prunus Virginiana 

Paeonia Officinalis Ptelea Trifoliata 

Pareira Brava Pulsatilla 

Parietaria Officinalis Pulsatilla Nuttalliana 

Paronichia Illecebrum Pyrus Americana 

Parthenium Quassia Amara 

Passiflora Incarnata Quebracho 

Pastinaca Sativa Quercus Robur 

Paullinia Pinnata Ranunculus 

Paullinia Sorbilis Ratanhia 

Pecten Rap Hanns 

Pediculus Capitis Rhododenrom 

Penthorum Sedoides Rhus Aromatica 

Persea Americana Resina Laricis 

Petroselinum Sativum Rhamnus Californica 

Phaseolus Rhamnus Cathartica 

Phellandrium Aquaticum Rhamnus Purshiana 

Physalis Alkekengi Rheum Officinale 

Phytolacca Ricinus Communis 

Pichi Robinia Pseudoacacia 

Pimenta Officinalis Rosa Canina 

Pimpinella Saxifraga Rosa Damascena 

Pinus Lambertiana Rosmarinum Officinalis 

Pinus Sylvestris Rubia Tinctorum 

Piper Methysticum Rumex Acetosa 

Piper Nigrum Rumex Crispus 

Piscidia Erythrina Rumex Obtusifolius 

Plantago Major Russula Foetens 

Platanus Ruta Graveolens 

Plectranthus Fruticosus Sabadilla 

Plumbago Littoralis Sabal Serrulata 

Polygonum Punctatum Salix Alba 

Polygonum Sagittatum Salix Nigra 

Populus Candicans Salix Purpurea 

Potentilla Anserina Salvia Officinalis 

Pothos Foetidus Sambucus Canadensis 

Primula Obconica Sambucus Nigra 

Primula Veris Sambucus Nigra 

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Sanicula Thlaspi Bursa Pastoris 

Sarracenia Purpurea Thuja Occidentalis 

Sarsaparilla Tilia Europaea 

Sassafras Officinale Tormentilla 

Schinus Molle Torula 

Scolopensrium Vulgare Trifolium Pratense 

Scutellaria Lateriflora Trifolium Repens 

Sedum Acre Trillium Pendulum 

Semper Vivum Tectorum Triosteum Perfoliatum 

Senecio Aureus Triticum Repens 

Senecio Jacobaea Tropaeolum Majus 

Senega Officinalis Turnera 

Senna Tussilago Farfara 

Sepia Tussilago Petasites 

Sinapis Ulmus Fulva 

Sinapis Nigra Uricum Acidum 

Skookum Chuck Urtica Dioica 

Solanum Carolinense Urtica Urens 

Solanum Mammosum Usnea Barbata 

Solidago Virgaurea Uva Ursi 

Spartium Scoparium Valeriana Officinalis 

Spigelia Marilandica Verbascum Thapsus 

Spilanthes Oleracea Verbena Hastata 

Spinacia Verbena Officinalis 

Spiraea Ulmaria Viburnum Opulus 

Stellaria Media Viburnum Prunifolium 

Sterculia Acuminata Viola Odorata 

Sticta Pulmonaria Viola Tricolor 

Stigmata Maidis Wiesbaden 

Stillingia Sylvatica Wyethia Helenioides 

Sumbul Symphoricarpus 

Xanthoxylum Fraxineum 

Racemosus 

Symphytum Officinale Yucca Filamentosa 

Taraxacum Officinale, Radix Yohim Binum 

Taxus Baccata Zingiber Officinale 

Teucrium Marum 

Teucrium Scorodonia 

Thaspium Aureum 

Thymus Serryllum 

Thea Sinensis 

Theobrominum 

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SUMMARY 

As can be seen from this brief list of examples, much of homeopathy is 

not always reversal; much of it is very similar to the action of herbal 

therapy. 

In herbal homeopathy, the minimal dose of an herb can achieve an 

effect. Herbology and homeopathy might join forces to become a more 

powerful form of medicine. 

In 1962, the FDA developed a new Food and Drug Cosmetic Act, which 

let homeopathy in the HPUS, as well as the USP (United States 

Pharmacopeia). In 1962, they did not include the Natural Compendium 

of Herbs which was supplied before 1962. This was because of an 

inability of herbalists to agree and to actively support themselves in the 

development of their Natural Compendium. 

Now we are going to provide a new description and definition of 

homeopathy which includes herbal precepts and reinstate herbalism 

under our new HPUS guidelines. Since homeopathy and herbalism share 

so much, and since the HPUS provides a legal backdrop for doctors to 

have NDC (National Drug Code) coded formulas within the HPUS, it is 

possible to include these different herbs and their activity within our 

guidelines. 

Homeopathy need not always involve using dramatically dilute 

substances. Mother tinctures, 1x, 2x, and 3x, are often high 

concentrations and yet this is still homeopathy. 

Let us explore the description of an opposite to homeopathy, which is 

allopathy. In allopathy we are working against the body, just as the 

allopath might use an antihistamine when the patient has a histamine 

response. By using an outside intervention the practitioner intervenes 

with the body so that the body will have time to heal itself. Thus, if there 

is a histamine response due to some causative factor, the allopath would 

use an antihistamine to help block the histamine, hoping that he/she 

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provides enough of a buffer to stall, so that the body can overcome the 

disease. Allopathy is not dealing with the true cause (rarely is the cause 

of the disease the fact that the person is deficient in the antihistamine or 

other drug). Oftentimes, histamine release is prompted by allergic 

activity, nutritional disturbances, chemical imbalances, and the like. The 

patient can sometimes build a dependence on these allopathic 

medications, as they will help the symptom, not the disease, and thus, 

will build dependence. This can often be beneficial to the synthetic 

chemical companies, but not to the patient. 

Allopathy seeks to provide an outside intervention from the smart 

doctor to the “stupid” patient’s body, to try to sedate, block, stimulate, 

trick or fool the system with a synthetic pharmacological agent. Allopathy 

can be seen as a heterogeneous type of medicine in which the 

intervention comes not from within the system, but from outside the 

system. In homeopathy, however, we provide the minimal dose of activity 

from our agents to allow the human system of the patient to achieve its 

balance through its own cybernetic feedback control. 

Homeopathy develops healing forces from within, or homogeneously, 

whereas allopathy does it from outside, or heterogeneously. The 

homeopath tries to work with the patient’s body to stimulate it towards 

healing and homeostasis balance. The principle of homeostasis implies 

that the body will seek to try to balance its activity along the lines of a 

certain degree of function. Thus, in maintaining calcium balance, the 

parathyroid and thyroid hormones will help to regulate calcium, 

oftentimes by taking calcium out of the bone to maintain serum calcium 

or by appetite control to drive the appetite toward different foods to 

balance our calcium intake. A very intricate sense of balance is needed 

for the extremely complex job of homeostasis. 

The whole principle of homeopathy relies on the study of homeostasis. 

In homeopathy, an herb is used only to provide the stimulus for the body 

to heal itself. The minimal dose is sought. Thus, Eyebright might help to 

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supply the needed nutrition and the needed pharmacological agents to 

help the patient’s body to rejuvenate its optical system, and achieve 

health. This implies a homogenous stimulation of homeostasis which is 

homeopathy. 

Our definition of homeopathy is: “Homeopathy is the medical art of 

gently stimulating the patient’s body toward balance and homeostasis.” 

Some dictums of homeopathy: 

� The human body is complex beyond our understanding, so we 

must work reverently with it to encourage health and balance from 

within. 

� Disease results from violation of natural law, and disease 

symptoms are a message from the body as it attempts to deal with 

the causative agent. Symptoms are beacons and traffic signals 

which point to cures. Symptoms are not the enemy as believed by 

allopaths. 

� Cure must come from removing or reducing the cause of disease, 

and then stimulating balance and homeostasis. 

� The healing of nations shall come from the leaves of the field. Only 

nature knows the intimate details of cure, and only nature can 

manufacture truly curative agents. 

� Homeopathy, herbology, acupuncture, and naturopathy have more 

in common than originally believed. Together with other similar 

modalities they represent a new era in medicine. 

Our broadened viewpoint of homeopathy lets the techniques of 

herbology to be used to their fullest proficiency. This allows the different 

herbal manufacturers to have a professional naturopathic and 

homeopathic philosophical governmental agency through the HPUS to 

guide them in quality control and legal direction. This broad-based 

definition of homeopathy has existed for years, and yet because of the 

mystery of homeopathy in like treating like, oftentimes it is categorized 

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as only like treating like. With this new, broader definition, and by 

utilizing the forces of different homeopathic practitioners and 

manufacturers to propagate this definition to the American public, they 

can get a better idea of how homeopaths are able to help in dramatic 

ways to stabilize and balance their bodies. Our herbal repertoire also will 

bring Chinese herbals into the system and let legally controlled 

manufacturers supply quality Chinese herbs with a proper national drug 

code to doctors. 

It is hoped that this chapter and the rest of this Natural Repertory will 

help to clear up some of the myths and misunderstandings in regard to 

homeopathy in its practical use. Homeopathy represents an inexpensive 

modality of medicine which is safe and effective in treating a wide variety 

of medical ills. In the 1990s, the American culture was severely 

threatened economically, and overburdened by a medical system that 

clung to allopathic synthetic pharmacology and surgery. These measures 

are not only drastically expensive and environmentally unsafe, but they 

are not cures. Allopathy is needed in medicine as a last resort in keeping 

some patients alive. The baby must not be thrown out with the bath 

water. Allopathy will always be a part of medicine. But allopaths should 

learn the fallacies of their techniques. They do not seek to bring patients 

to balance or cure. They only seek to develop dependency on different 

items in the lost hope that patients’ bodies can regain balance before the 

synthetic drugs do their damage to kidneys, liver, nerves and digestion. 

Allopaths treat symptoms. To this end, homeopathy offers economic 

solutions, the development of safe and effective modalities, and help in 

returning to a system of reverence for the natural process of our bodies 

and the natural process of the ecological system of the world. 

One day medicine might overcome its egocentric biases, and teach all 

techniques and philosophies together under one true medicine. A new 

day will dawn in which healers will learn to appreciate each other and 

help patients, rather than propagate egos. 

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AN ADVANCED TREATISE IN QUANTUM BIOLOGY 

The Quantic Link to DNA 

The father of quantum theory was Erwin Schrödinger. He believed that 

there was a definite link between quantum theory and DNA. As we have 

reviewed several parts of biological literature in this book, we now would 

like to review a brief introduction on quantum theory and genetic coding. 

Here we see the best demonstration of a quantum biological function, as 

the formation of the DNA code does not utilize half-steps; it makes 

distance coding jumps. There are distinct patterns in the DNA code that 

allow for exacting patterns. In hereditary techniques we can see that 

there is a preciseness of transfer which yet has some degree of 

indeterminacy. As we have discussed in the Quantum Biology and in this 

workbook, there must be a metabolic side as well as a reproductive side 

to our matrix, so that the metabolism can respond to a wide variety of 

different types of environmental conditions. But the genetic coding would 

have to have very limited, predictable and distinct types of jumps. It 

would have to be a more precise and closed process. We have already 

discussed this in some detail (see Quantum Biology). Now, let us review 

some of the literature which has led to our understanding of DNA 

function. 

In the early days, there were three categories of food: oleaginous (fats), 

saccharinous (carbohydrates), and albuminous (protein). The 

development of protein was a key factor in the development of life. It is 

protein which is analyzed in our treatise on DNA. Jöns Jakob Berzelius 

proposed the names of cystein and glycine as he was doing research on 

amino acids. In 1838, he coined the word “protein”, which is Greek for 

primary substance. He found that this was the basic unit of all 

albuminous material. Gerardus Johannes Mulder, also working in the 

very early 1800s, continued some of the Berzelius work. He proposed a 

198

asic albuminous substance with an empirical formula C40H62N10O12; this 

combined with many other formulas produced some of the basic proteins 

of life. 

In the 1890s, Emil Fischer, who was once a student of August Kekulé, 

found that there were dextro and levo types of polymers. He was the first 

to find that there was a chirality, or “handedness” to nature. He then 

found that this “handedness” also applied to protein compounds. 

In the 1850s, Thomas Graham found crystalloids and colloids, and 

studied their functions. Colla came from the Greek for glue. Theodor 

Svedberg contributed evidence to the theory that proteins were 

homogenous. Using Avogadro’s number and the weight of the large 

colloidal particles, he determined their diffusion rate and sedimentation 

as a constant in the earth’s gravitational field, producing up to 500 times 

the force of gravity. He then separated these colloidal factors, and helped 

to further the concept of homogeneity. 

By 1936, Linus Pauling and Alfred Mirsky put forth the idea that 

polypeptide chains of native proteins could be folded and held together 

between the N/h group and the oxygen atom of the C//O group of 

peptide bonds. Many different scientists, including Corey and Perutz, 

started working with these large chemicals and proposed some of the 

different fashions which led to the discovery of the helix. 

John Kendrew was the first to find the three-dimensional structure of 

myoglobin which has an approximate molecular weight of 17,500. He 

found that 75% of myoglobin has a helical polypeptide chain. Thus, the 

helix was further brought into science. 

The three-dimensional structure of insulin was discovered in 1969, by 

Dorothy Crowfoot Hodgkin, working at Oxford University. Other bio- 

molecules were found, such as cholesterol, calciferol, penicillin, and B- 

12, using x-ray photographs of the diffusion patterns of the insulin 

crystal. Dorothy Hodgkin was able to propose the structure of this very 

complex molecule. Insulin was the first native protein to be synthesized. 

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In 1966, Robert Bruce Merrifield developed insulin by means of a 

machine which was designed to carry out polypeptide synthesis. 

Synthetic chemistry was well underway, and the precept of synthetic 

chemistry to this day has been that of placing the calcium, carbon, and 

hydrogen in the right spots. This was achieved by looking at the x-ray 

photographs and diffraction patterns, doing spectrographic analysis, and 

other different functions. But they were not able to discern the type of 

energy that existed in the quantic bonds, or of the electrons in their 

outer rings. Nature still has many secrets. 

Some of the different quantic energy patterns of the natural substances 

still were unknown to these synthetic developers. The synthetic 

developers sought to develop synthetic compounds but found that they 

were not as effective as natural entities. This did not hinder them in the 

least; they achieved extreme financial success through their synthesis. 

They were able to develop and manufacture compounds and live off 

rather rich royalties as these synthetic compounds were sold as 

medicines. As they reduced the complex world of natural biology into 

synthetic components they developed more and more compounds. Many 

were to follow after insulin. 

Let’s take a look at some of the first work that was done with insulin. It 

was founded to be only 3.4% effective at best in the early crystalline 

structure designed by Merrifield. Later, in the 1960s, scientists started to 

dispel the idea that organic substances were different from the synthetic 

matter which they were developing. Because of the limits of their thought 

and the limits of their techniques of measurement these compounds 

appeared to be equal. This is not the case in the 1990s. With our 

sophisticated energy equipment and methods of discerning the energy 

patterns and electrical responses of compounds, we now find that nature 

does indeed have some rather complex safeguards and complex secrets 

which the synthetic chemical companies have yet to divine. 

200

In 1986, Carl Popper delivered an address to the Royal Society. In this 

address he told the attendees, who included many of the fathers of 

synthetic molecular biology, that biochemical organizations and 

processes could never be understood in chemical terms alone. Because of 

this, Popper proposed that organic evolution would never be explained by 

chemical or Darwinian Theory and that chemical reductionism for the 

environment proposed many different risks, as we put many of these 

synthetic chemicals into our environment and our bodies. In fact, due to 

the large number of chemicals which have been put into our bodies, 

perhaps Carl Popper’s warning has come too late. Many dramatic 

problems have resulted from iatrogenic poisoning of the planet and 

iatrogenic diseases which were caused by synthetic compounds. 

Dramatic damage has resulted from ignorance and profiteering. 

Man’s ability to understand is always limited by his ability to measure 

the results of his work. At every point in science the scientists assume 

that their measurements are complete, therefore their knowledge must 

be complete. As new discoveries are made and more sophisticated 

measurement techniques are developed this philosophy opens the door 

to deeper and deeper understanding. With the advent of quantum theory 

and the idea of the Heisenberg Uncertainty Principle we now realize that 

true knowledge cannot be attained, and that we cannot in any way 

manufacture the same compounds developed by nature. Our attempts at 

this are merely guesses, perhaps good guesses but still, nature holds 

secrets as we continue to explore biology to the end of our days. Only 

nature truly knows. 

In 1893, Albrecht Kossel, doing physiological research identified 

chromatin as a nucleoprotamine. This was found to be a nucleoprotein, 

and was some of the beginning work needed in looking at RNA and DNA 

function. 

Nucleic acid sugars and their phosphate-bonded brothers were written 

about by Phoebus Levene in 1905. Levene, working with Walter A. 

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Jacobs, classified sugar of yeast nucleic acids as D-Ribose. This is linked 

to the bases by a glycosidic bond. They termed these nucleosides. 

Adenosine, guanosine, cytidine, and uridine, when esterified by 

phosphates, became adenylic acid, guanylic acid, cytidylic acid, and 

uridylic acid. It was Levene who later found that this sugar is RNA and 

DNA was not a hexose, but a pentose. 

Early determinations of the molecular weight of DNA gave values of the 

order of 10 3. In 1938, Frederick Sanger proposed that its weight was 10 6 . 

Levene also was able to confirm this new molecular weight in 1938. 

In 1944, at the Rockefeller Institute Hospital, Oswald Avery came up 

with the first strong evidence that DNA was really the key to transferring 

genetic characteristics in microbes. Avery also proposed some of the DNA 

enzymes, such as DNA depolymerase and deoxyribonuclease. These 

enzymes were found to deactivate DNA, but were later key in the process 

of unfolding and unwinding the DNA to set genetics in motion. 

In 1945, DNA was found to have light absorption in the area of 260 

nanometers, and to have some mitogenic-like production of UV. These 

purines and pyrimidines were also found to have strong light 

relationships; both absorption and production. 

Erwin Chargaff in 1950 was able to show some of the strong light 

spectrophoto reaction of the different components of DNA and DNA itself. 

From this, the research finding adenine, guanine, cytosine, and thymine, 

or A, G, C, and T, led to the discovery of the different Chargaff rules. 

First, the total of purines and pyrimidines are quantitatively equi- 

molecular; that is, A + G = T + C. Second, the molecular quantities of 

adenine and thymine individually are equal: A = T. Third, the amounts of 

guanine and cytosine are molecularly equivalent; G = C. A relation of the 

preceding rules comes to the final rule in which A + C = G +T. Later, it 

was found that uracil took the place of thymine in the RNA components 

of the cell. These rules echo our quantum rules in many ways. 

202

Many people around 1950 were struggling to find ways of 

understanding this. But it was Crick and Watson at Cambridge who best 

improved on Pauling’s research, using the Chargaff rules and developing 

a consensus idea of the structure of DNA. They proposed a double helix. 

This opened the door for dramatic understanding. 

The mechanics of this process could be easily understood by the 

mechanically-minded scientists of the time. Yet, this type of mechanical 

process did not appear in any other chemical process. Chemical 

processes were known to be statistical, or involving random development 

of compounds which were pushed and pulled apart through entropic or 

thermodynamic processes. This strand of DNA does not do this; it is not 

a randomized process. It pulls apart and pushes together in a very 

precise maze. The actual mechanisms of this push and pull were not 

studied by these scientists; they liked the idea of the chemistry involved. 

But now, we can ask the question: Through what processes is DNA 

pushed/pulled apart? The answer leads to quantum dynamics. Our 

quantic analysis matrix can be superimposed on the DNA action. 

Research blossomed into the concept of the mechanics of DNA. As 

Isaacs has told us, the E. coli is an example of a type of near vion from 

cells, meaning the base amount of matter needed to actually make up a 

living unit which could metabolize and reproduce on its own. Inside the 

E. coli is a double–stranded DNA chromosome which contains 4 x 10 6 

base pairs. It will reproduce at maximum rate of 750 base pairs per 

second. This is at a given unwound replicating fork region. So it will take 

about forty minutes to reproduce a complete chromosome. If the 

conditions are right, E. coli will divide into two daughter cells every 

twenty minutes. This is the nature of vionic activity. 

In 1953, Paul Zamecnik, working at Harvard University, tried to put 

radioactive isotopes of different amino acids into a bacteria colony. This 

was an attempt to trace the radioactive polypeptides through the 

different ribosomes. The experiment was a failure because by putting in 

203

the different radioactive isotopes the RNA functioning came to a halt. It 

could only be brought back by bringing in a fresh, natural selection of 

the amino acids. Thus, DNA has some ability to possibly ‘know” that the 

items involved are radioactive. This would be reinforced by our quantum 

theories; if a radioactive particle were put into this process, the biology 

would soon be able to “know” it and halt its progress. Biology and life 

operate on many levels including sub molecular. The process would be 

able to notice radioactivity as an irregularity. 

This makes us wonder about the different radioactive tracing 

experiments in which radioactive iodine was put into the body by 

experimenters who found that it goes to the thyroid; and then it was 

assumed that all iodine would go to the thyroid. All we know from that 

experiment is that radioactive iodine goes to the thyroid. We do not know 

where normal iodine goes. This is another limitation of quantic theory. 

Tracing experiments have led to many faulty conclusions in biology. 

Electron microscopists started to come up with ideas of transcription 

and translation of the ability to handle RNA and DNA. But basically, at 

the relative body temperature E. coli’s DNA is transcribed at a rate of 

around sixteen nucleotides per second into the messenger RNA strand. 

The messenger RNA strand has an average length of 2,000 to 3,000 

nucleotides. The half-life of the messenger RNA strand is about 90 

seconds. So the ten to fifteen ribosomes which are in the process of 

translating with a given messenger RNA and forming a polyribosome 

become attached to the strand during the period of transcription from 

the DNA. Polypeptides formed by each ribosome of a polyribosome 

system are the same. The formation time of a polypeptide is around ten 

seconds under certain prime conditions. 

The growing E. coli bacteria contain some 15,000 ribosomes. They 

make up 25% of the cell mass. The ribosome is approximately 20 

nanometers across and has a molecular weight of 2.7 x 10 6 . 

204

By 1966, many of the details of the genetic code were worked out, 61 

out of the total 64 triplet codons. 

From the late 1950s, the sequence of amino acids in proteins with a 

specific function, such as insulin, hemoglobin, or cytochrome c, were 

determined and catalogued by a range of organisms followed a decade 

later by corresponding determination of nucleic acid sequences. In 

analyzing the sequences then available, Zuckerkandl and Pauling (1965), 

pointed out that a present-day protein contains its own ancestral history 

in its quantic organization, and that similarities of homologous 

polypeptide chains along with the accepted fossil record provide 

evolutionary data of three types. 

� The probable amino acid sequence of the ancestral polypeptide 

from which the chains compared had diverged. 

� The approximate epoch at which the divergence started. 

� The lines of descent through which the alterations in amino acid 

sequence proceeded. 

The vast extent of data storage and processing that was proved in our 

quantic chapter easily allows for this process. 

Zuckerkandl and Pauling calculated a mean substitution rate for a 

hemoglobin polypeptide of one amino acid every 14.5 million years from 

the 18 residue differences attained in comparison of the horse and the 

human α−chain. It was known that the α− and the β−chains of the 

human hemoglobin tetramer (α2β2) show 78 differences so one can 

surmise that the two polypeptides originally split from a common origin 

by gene duplication at least 565 million years ago. Originally, the 

common point was monomeric hemoglobin consisting of a single 

polypeptide chain. This chain has a more modern representation in the 

blood of primitive jawless fish (the lamprey and the hagfish, which lack 

the advantage of cooperative oxygen uptake and release that emerged 

with the evolution of the hemoglobin tetramer). 

205

A similar technique to that of Zuckerkandl and Pauling with their 

construct of a ‘molecular evolutionary clock’ was put forward by Motoo 

Kimura. They used a Poisson distribution. Thus, the events of low 

probability in a vast population like the decay of radioactive isotopes 

used to calibrate the geological evolutionary clock are mathematically 

calculated. Kimura posted that for two homologous polypeptides made of 

n residues with varying amino acids at d sites due to bifurcation over a 

time t, the rate of evolutionary amino acid substitution per site per years, 

kaa, is given by the relation 

2tkaa = -1n(1 – d/n) - -2.31og(1 – d/n). 

This equation, applied to a series of sequenced polypeptides with a 

common biochemical role such as the α−chain of vertebrate hemoglobin 

will result in a constant value of kaa of the order of 10 -9 residue 

replacements per site per year, a unit that M. Kimura termed the pauling 

or the ‘molecular evolutionary unit’ (MEU). This is allowed for in our 

bioquantic matrix. Life must allow for some minute variations to occur in 

its reproduction accounting system. Varying slightly for a given type of 

protein, the value of the kaa varies readily for proteins of contrasting 

functional types by three orders of magnitude. This ranges from the 

rapidly evolving fibrinopeptides (8.3 MEU) to the well conserved histone 

proteins (0.009 MEU). The fibrinopeptides are key in the formation of 

blood clots, and only a minuscule part of the polypeptide has an 

essential function. The amino acids of the other segments freely undergo 

substitution without the benefits of selective control. This process 

involved no drastic functional changes. Comparatively, histone 

polypeptides are essential in the conservation of the genetic material, 

making up the nucleosome particles where the double-stranded DNA 

supercoils in the eukaryote nucleus to provide the nucleoprotein 

chromatin whereby a ‘string of beads’ form. 

206

The MEU, or one Pauling, is a definite quantic type of function. Our 

bioquantic matrix must tolerate some limited variations. These variations 

can result in genetic improvements from genetic bifurcation (see 

“Fractals” in Quantum Biology). But, for these variations to last they 

must result in increased productivity. Increased productivity comes from 

cooperation with the environment, not superiority. So Darwin was wrong 

about survival of the fittest. Now, we can say that there is survival of the 

adaptive and cooperative. 

The histone proteins are stabilized and conserved. They have only two 

differences out of about 100 amino acids in the H4 polypeptide between 

calf thymus and the pea plant even though animals and plants split 

apart some 1.2 billion years ago. 

Contrasts of the mRNA sequences coding for the histone H4 

polypeptide in two sea urchin species demonstrates that the synonymous 

mutation rate in the DNA transcribed is as high as that of the fast 

evolving fibrinopeptides. The degeneracy of the genetic code is eminent 

for the third position (3’ –end) of the coding base triplets. Here the 

transitional mutations (U/C) or (A/G) are mostly inert. Comparison of 

the mRNA sequences coding for the α− and the β−polypeptide chains of 

mammalian haemoglobin demonstrate that natural selection has lowered 

the rates of surviving base changes in the first and second positions of 

the triplet codons which are approximately equal+ to one-quarter or less 

of the mutational rate found for the third codon position. Quantum 

theory is consistent with such processing. Schrödinger was right in 

assuming that genetics is a quantic activity. Genetics or reproduction 

requires an exacting and limited process. Metabolism requires vast 

responsiveness. 

The archaebacteria characteristically thrive in extreme environments, 

hot sulphurous vents, salt marshes, or anaerobic organic-rich muds. 

Archaebacteria are ancient, as the term archae implies. They have 

207

heterogeneity of their 16S rRNA sequences due to divergence over aeons. 

As Isaacs points out jumps in species and genes also must follow quantic 

law. The indices of those 16s rRNA sequences distinguish three major 

divisions: 

� The methanogens and halophiles 

� Thermoplasma, a group containing a single organism 

� A heterogeneous group of sulphur-dependent 

thermoacidophiles, probably the most ancient of the 

prokaryotes 

These bacteria can live under acidic conditions (pH 1-6) and at elevated 

temperatures (60-95 ºC). Sulfolobus oxidizes sulphur to sulphate while 

others reduce sulphate to sulphide, like Archaeoglobus which develops 

small quantities of methane as well. These are some of the extremes of 

life, or conditions in which the matrix of life can operate. 

The 16S tRNA sequences of the eubacteria indicated that, while Gram 

positive organisms form a distinct group of related species, gram negative 

organisms are much more diverse. The break into nine groups is defined 

by a common coefficient of 0.2-0.3 within a group. Most Gram negative 

bacteria belong to the purple bacteria group which has not only the 

colored photosynthetic organisms but also many colorless analogues. 

Samples of these analogues are E. coli and other enteric bacteria. The 

green photosynthetic bacteria also go into two distinct groups ~ 

� Sulphur (hydrogen sulphide substrate) 

� Non-sulphur (organic substrate) types 

which are not closely related (SAB 0.18). The cyanobacteria consist of a 

coherent group, and they are similar to the chloroplast organelles of 

eukaryotic red and green algae, and green plants (SAB values of 0.25 – 

0.30). If a quantum leap is performed in the genetic code of bacteria, 

then this will result in a new type of bacteria. 

The sulphate-reducing bacteria which use the oxygen of the sulphate 

for a primitive form of respiration comprise a Gram negative eubacterial 

208

group. A type of bacteria in this group, Desulfovibrio sulfodismutans, can 

attain free energy from the disproportionation of sulphite or thiosulfate to 

sulphide and sulphate. This is an ‘inorganic fermentation’ process 

similar to the redox disproportionation of glucose to ethanol and carbon 

dioxide (Bak and Cypionka 1987). 

Thus, we can plot genetic changes on a hermitian matrix. This allows 

us to develop new energetic laws of biology. 

The eukaryote organelles, the mitochondrion, and the chloroplast all 

share a prokaryote size (1 μm). They are vions that contain their own 

DNA. These vions also have a circular double strand as in bacteria, and 

ribosomes of the bacterial type. The 165 rRNA sequences of the 

organelles tell us that the mitochondria belong to the purple group of 

eubacteria and the chloroplasts to the group of cyanobacteria. 

Indigenous DNA in the organelles and the sameness of their 16S rRNA 

sequences to those of extant eubacteria led to the theory that 

mitochondria and chloroplasts evolved by a process of endosymbiosis. 

This theory hypothesized that ancestral eukaryote with a vacuole 

nutrient method of securing nutrients into a membrane-bounded vacuole 

once engulfed a purple-group aerobic bacterium generating ATP through 

the respiratory chain. As the guest supplied ATP, the host archae- 

eukaryote provided back to the guest proto-mitochondrion the materials 

required for its maintenance and ATP production. So, mutual vionic 

patterns merged for symbiotic cooperation. The phagocytosis of a 

cyanobacterium into a vacuole led to the development of the chloroplast, 

which supplied carbohydrate to its host. In return, the cyanobacteria 

supplied a life-support system. The two membranes around the organelle 

are leftovers of the endosymbiotic beginnings. The inner membrane 

represents the cytoplasmic membrane of the eubacterial guest. The outer 

membrane corresponds to that lining supplied from the vacuole of the 

host eukaryote. In vionic coupling sometimes functions can be presented 

209

dually. Quantum laws can still be obeyed. Backup systems are 

abounding in biology. 

Possible relatives of the ancestral eukaryote, as many as a thousand 

species, have no mitochondria or other organelles. These species split 

from vion tendency to form the archaezoa subdivision of the eukaryotes, 

just as the metakaryota, which contain mitochondria, is an example of a 

vion. Sequenced representatives of the archaezoa are minute parasites of 

the metamonada and the microsporidia. These vions contain bacterial – 

sized ribosomes with 16S rRNA in the smaller subunit. They don’t have 

the 18S rRNA found in the higher eukaryotes. The 16S rRNA sequences 

of a microsporidia and a metamonada species differ greatly from 

mitochondrion – containing eukaryotes, the metakaryota. This suggests 

an early vionic divergence. The archaezoa and the metakaryota split 

before the age (1.4 billion years) of the larger microfossils (10 μm) which, 

on account of their size probably represent the remains of organelle – 

equipped eukaryotes (Cavalier–Smith 1989). We can see this vionic 

divergence in our matrix. 

Biochemically, the eukaryotes share similarities with both the 

eubacteria and the archaebacteria. The translation of mRNA into a 

polypeptide starts with methionine in the eukaryotes as it does in the 

archaebacteria. But translation starts with N – formylmethionine in the 

eubacteria. Elongation of the polypeptide chain is stopped by dipthera 

toxin in the eukaryotes and the archaebacteria but not in the eubacteria. 

Chloramphenicol stops the elongation in eubacteria but not in 

eukaryotes or archaebacteria. The lipids of the cytoplasmic membrane in 

both eubacteria and eukaryotes contain the diesters of L- 

glycerophosphate with straight-chain fatty acids. In contrast, the 

archaebactrial lipids are composed of the diethers of D-glycerophosphate 

with phytanol and other branched-chain alcohols. The variance of vionic 

210

technique in metabolism responsiveness is pointed out here. The quantic 

interchange of environmental forces can have a wide range of activity. 

The analysis of DNA and its function has received extreme scrutiny 

from the scientific community over the last twenty-five years. Many 

different abilities of DNA have been described and experimentally 

ascertained. 

One of the most recent advances in DNA is that of gene splicing, 

wherein genetic engineering can be accomplished by taking out a bad 

gene and splicing a healthy gene into the DNA. This dramatic new 

research offers great potential for medicine in correcting metabolic or 

genetic disorders. 

Modern medicine has also developed the technique of splicing the gene 

into a virus and allowing the virus to penetrate into the cell membrane, 

and to create a new gene code which will replace the diseased code with 

a healthy genetic code. 

But with all this dramatic research being done with DNA, scientists 

have done little to account for the phenomenon of how the transmission 

of genetic data can be accomplished. For this, we can go to Schrödinger 

and his description of the quantum abilities of DNA. This we have 

outlined in the chapters of his book to give a basic understanding. 

Our description of the quantum philosophy and the quantum 

dynamics will let us find and be predictive of the long range forces in 

biology that account for the function of DNA. The development of the 

matrices will also help explain some of the DNA functioning. 

211

SUMMARY - THE QUANTIC LINK TO DNA 

� We reviewed the literature and the thought processes which 

arrived at the different philosophical understanding of DNA, 

leading to today’s use of chromosomal therapy in medicine. 

� We outlined the possible ways that Schrödinger was right about 

DNA working on quantum levels. Genetic transfer of the DNA is 

accomplished by quantum dynamics. 

� We outlined a basic mathematical precept to understand this 

quantic link to DNA. Thus, we attempted to explain genetics 

through quantum theory. 

� A proposition was outlined on how DNA function can be further 

analyzed, not just from the chemical dynamics, but also from an 

energetic, quantum dynamics to further understand how to correct 

these situations in the future. A possible new DNA therapy is 

hinted at by using chromosomal homeopathy. 

Bibliography 

Bak, F. Cypionka, H. A novel type of energy metabolism involving 

fermentation of inorganic sulphur compounds. Nature. 1987; 326:891- 

892. 

Cavalier-Smith, T. Molecular phylogeny. Archaebacteria and Archezoa. 

Nature. 1989; 339(6220):100-1. 

Zuckerkandl, E. Pauling, L. Evolutionary divergence and convergence in 

proteins, 1965; 97-166 In: Evolving Genes and Proteins, edited by V. 

Bryson and H.J. Vogel. Academic Press, New York. 

212

THE HUMAN GENOME 

How to interpret the index and map 

Disorders that appear within square brackets [ ] represent “non-diseases” 

– mainly genetic variations that lead to apparently abnormal laboratory 

test values (e.g., dysalbuminemic euthyroidal hyperthyroxinemia). 

Disorders printed inside boxes in the map represent allelic disorders, 

which can result in multiple, quite dissimilar disorders from the various 

mutations in the same gene. Disorders printed within braces { } represent 

genetic mutations that make affected individuals susceptible to a specific 

disease, infection or other condition (e.g., coronary artery disease). A 

question mark ? before the disorder means that confirmation of a gene or 

locus is uncertain or in dispute. Although all known or suspected genetic 

disorders appear in the index, some do not appear on the map if their 

chromosomal location is particularly controversial. Moreover, on the 

ideogram of chromosome X, some disorders have been left out to 

conserve space. These excluded disorders are included in the index and 

marked with an asterisk *. Disorders printed in bold were added to the 

list in the past year. Those printed underlined have been changed in 

location on the chromosomes in the past year. Finally, each disorder in 

the index is followed by one of three numbers in parentheses that 

indicates whether the mutation was located by mapping (1) wild-type 

gene, (2) the disease phenotype, or (3) both approaches. 

213

ALPHABETICAL INDEX OF HEALTH DISORDERS 

AND CHROMOSOME LOCATION 

Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency (1) 8q21 

Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency (3) 6p21.3 

3-hydroxyacyl-CoA dehydrogenase deficiency (1) Chr.7 

*46, XY female (2) xp22.2-p21.3 

Aarskog-Scott syndrome (2) Xq13 

?Abetaa Lipoproteinemia 2p24 

[Acanthocytosis 1 form] (1) 17q21-q22 

Acatalasemia (1) 11p13 

Acetyl-CoA carboxylase deficiency (1) 17q21 

Acid-maltase deficiency, adult (1) 17q23 

Acoustic neuroma (2) 22q11.21-q13.1 

?Acrokeratoelastoidosis (2) 2p 

ACTH deficiency (1) 2p25 

Acute alcohol intolerance (1) 12q24.2 

Acute Lymphoblastic Leukemia (2) 9p22-p21 

Acute Promyelocytic Leukemia (1) 17q21.1 

Acute Promyelocytic Leukemia (2) 15q22 

Acyl-CoA Dehydrogenase, medium chain, deficiency of (1) 1p31 

Acyl-CoA Dehydrogenase, short chain, deficiency of (1) 12q22-qter 

Adenylosuccinase deficiency (1) Chr.22 

Adrenal hyperplasia II (1) 1p13 

Adrenal hypoplasia, primary (2) Chr.10 

Adrenocortical carcinoma (2) Xp21.3-p21.2 

Adrenoleukodystrophy (2) 11p15.5 

Adrenomyeloneruopathy (2) Xq28 

[AFP deficiency, congenital] (1) Xq28 

Agammaglobulinemia, type 2, X-linked (2) 4q11-q13 

*Agammaglobulinemia, X-Linked (2) Xq21.3-q22 

Aicardi syndrome (2) Xq22 

214

Albinism (3) 11q14-q21 

Albinism-deafness syndrome (2) Xq26.3-q27.1 

?Aldolase A deficiency (1) 16q22-q24 

Allan-Herndon syndrome Xq21 

Alpha-1-antichymotrypsin deficiency (1) 14q32.1 

Alpha-NAGA deficiency (1) 22q11 

Alport syndrome (3) Xq22 

Alzheimer’s disease, type I (3) 21q21.3-q22.05 

*Amelogenesis imperfecta (1) Xp22.3-p22.1 

[AMP deaminase deficiency, erythrocyte] (1) 1p21-p13 

Amyloid neuropathy, familial, several allelic types (3) 18q11.2-q12.1 

Amyloidosis, cerebroaterial, Dutch type (1) 21q21.3-q22.05 

Amyloidosis, Finnish type (1) 9q34 

Amyloidosis, Iowa form (2) 11q23 

{?Amyloidosis, secondary, susceptibility to} 1q12-q23 

Amyotrophic Lateral Sclerosis (2) 21q21.1-q22.3 

?Anal canal carcinoma (2) 11q22-qter 

Analbuminemia (1) 4q11-q13 

Anemia, congenital due to deficiency of gastric intrinsic factor (1) Chr.11 

Anemia, sideroblastic/hypochromic (3) Xp21-q21 

Aneurysm, familial (2) 2q31 

Angelman syndrome (2) 15q11-q13 

Angioedema, hereditary (1) 11q11-q13.1 

Anhidrotic ectodermal dysplasia (2) Xq12.2-13.1 

Aniridia of WAGR syndrome (2) 11p13 

Aniridia-1 (2) 2p25 

Aniridia-2 (2) 11p13 

Anterior segment mesenchymal dysgenesis (2) 4q28-q31 

Antithrombin III deficiency, (3) 1q23-q25 

ApoA-I and apocC-III deficiency, combined (1) Chr.11 

Apolipoprotein B-100, defective (1) 2p24 

[Apoliproprotein H deficiency] (1) Chr.17 

Argininemia (1) 6q23 

Argininosuccinicaciduria (1) 7cen-q11.2 

Arteriohepatic dysplasia (2) 20p11.2 

Aspartylglucosaminuria (3) 4q23-q27 

Ataxia-telangiectasia (2) 11q22-q23 

Atopy (2) 11q12-q13 

Atransferrinemia (1) 3q21 

Atrial septal defect, secundum type (2) 6p21.3 

Autonomic failure due to DBH deficiency (1) 9q34 

215

?Batten disease, 1 form (1) 15q24-q25 

Batten disease (2) 16p11 

Becker muscular dystrophy (3) Xp21.2 

Beckwith-Wiedemann syndrome (2) 11pter-p15 

Bernard-Soulier syndrome (1) 17pter-p12 

?Bloom syndrome (1) Chr.19 

?Bloom syndrome (2) Chr.12 

*Borjeson-Forssman-Lehmann syndrome (2) Xp26-q27 

?Branchiootic syndrome (2) 8q13.3 

?Breast cancer (1) 17p13.3 

Breast cancer, ductal (2) 1p36 

Breast cancer, ductal (2) Chr.13 

Breast cancer, early onset (2) 17q21 

Brody myopathy (1) Chr.16 

Burkitt’s Lymphoma 8q24.1 

?C1q deficiency (1) 1p 

?C1q deficiency (1) 1p 

C1r/Cis deficiency, combined (1) 12p13 

C1r/Cis deficiency, combined (1) 12p13 

C2 deficiency (3) 6p21.3 

C3 deficiency (1) 19p13.3-p13.2 

C3b inactivator deficiency (1) 4p25 



C5 deficiency (1) 9q34.1 

C6 deficiency (1) 5p13 


C8 deficiency, type I (2) 1p22 

C9 deficiency, type II (2) 1p22 


?Campomelic dysplasia with sex reversal (2) 5q33.1 

?Campomelic dysplasia with sex reversal (2) 8q21.4 

Carbamoylphosphate synthetase I deficiency (1) 2p 

[Carbonic anhydrase I deficiency] (1) 8q22 

?Cardiomyopathy (1) 2q35 

?Carotid body tumor-1 (2) 13q34 

Cate eye syndrome (2) 22q11 

?Cataract, anterior polar (2) 14q24 

?Cataract, anterior polar (2) 2p25 

Cataract, Coppock-Like (3) 2q33-q35 

Cataract, Marner type (2) 16q22.1 

216

Cataract, zonular pulverulent (2) 1q22 

*?Cataracts, congenital total (2) Xp 

Central core disease of muscle (2) 19q12-q13.2 

Cerebral amyloid angiopathy (1) Chr.20 

Cerebrotendinous xanthomatosis (2) 2q33-qter 

[CEPT-deficiency] (1) 16q21 

Charcot-Marie-Tooth disease, slow nerve conduction type Ia (2) 17p11.2 

Charcot-Marie-Tooth disease, slow nerve conduction type Ib (2) 1q21.2-q23 

Charcot-Marie-Tooth disease, X-linked dominant (2) Xq13 

Charcot-Marie Tooth disease X-linked recessive 1 (2) Xq22.2 

?Chediak-Higashi syndrome (2) 1q43 

Cholesteryl ester storage disease (1) 10q24-q25 

*Chondrodysplasia punctata, X-Linked dominant (2) Xq28 

Chondrodysplasia punctata, X-Linked recessive (2) Xpter-p22.32 

Choroideremia (2) Xq21.2 

Chronic granulomatous disease due to deficiency of NCF-1 (1) 7q11.23 

Chronic granulomatous disease due to deficiency of NCF-2 (1) 1q25 

Chronic infections (1) 10q11.2-q21 

Citrullinemia (1) 9q34 

Cleft palate, X-linked (2) Xq21 

CMO II deficiency (1) 8q21 

*Coffin-Lowry syndrome (2) Xp22.2-p22.1 

?Coloboma of iris (2) 2pter-p25.1 

Colorblindness, blue monochromatic (3) Xq28 

Colorblindness, blue monochromatic (3) Xq28 

Colorblindness, blue monochromatic (3 Xq28 

Colorblindness, deutan (3) Xq28 

Colorblindness, protan (3) Xq28 

Colorblindness, tritan (2) 7q22-qter 

Colorectal adenoma (1) 12p12.1 

?Colorectal cancer (1) 12p12.1 

Colorectal cancer (1) 18q23.3 

Colorectal cancer (3) 17p13.1 

Colorectal cancer, familial (2) 5q22-q23 

Combined C6/C7 deficiency (1) 5p13 

?Combined variable hypogammaglobulinemia (1) 14q32.33 

Conductive deafness with stapes fixation (2) Xq13-q21.1 

Coproporphyria (1) Chr.9 

{Coronary artery disease, susceptibility to} (1) 6q27 

Cortisol resistance (1) 5q31 

CR1 deficiency (1) 1q32 

217

Craniosynostosis (2) 7p21.3-p21.2 

[Creatine kinase, brain type, ectopic expression of] (2) 14q32 

Creutzfeldt-Jakob disease (2) 20pter-p12 

?Cryptorchidism (2) Xp21 

[Cystathioninuria] (1) Chr.16 

Cystic fibrosis (2) 7q31.3-q32 

Debrisoquine sensitivity (1) 22q11.2-q12.2 

Dentinogeneis imperfecta-1 (2) 4q13-q21 

Diabetes insipidus, nephrogenic (3) Xq28 

Diabetes insipidus, neurohypophyseal (1) 20pter-p12.21 

?Diabetes mellitus, insulin dependent (2) 6p21.3 

Diabetes mellitus, insulin-resistant, with acanthosis nigricans (1) 19p13.3-p13.2 

Diabetes mellitus, rare form (1) 11p15.5 

?Diaphragmatic hernia (2) 1q32.3-q42.3 

Diastrophic dysplasia (2) 5q22-q34 

DiGeorge syndrome (2) 22q11 

Diphenylhydatoin toxicity (1) 1q22-qter 

[Diphtheria, susceptibility to} (1) 5q23 

?Dubin-Johnson syndrome (2) 13q34 

Duchenne muscular dystrophy (3) Xp21.2 

[Dysalbuminemic hyperthyroxinemia] (1) 4q11-q13 

[Dysalbuminemic hyperzincemia] (1) 4q11-q13 

Dysfibrinogenemia, alpha types (1) 4q28 

Dysfibrinogenemia, beta types (1) 4q28 

Dysfibrinogenemia, gamma types (1) 4q28 

Dyskeratosis congenital (2) Xq28 

?Dyslexia-1 (2) 15q11 

Dysplasminogenemic thrombophilia (1) 6q26-q27 

Dysprothrombinemia (1) 11p11-q12 

[Dystransthyretinemic hyperthyroxinemia] (1) 18q11.2-q12.1 

Ehlers-Danlos syndrome, type IV (3) 2q31 

Ehlers-Danlos syndrome, type VIIA1 (3) 17q21.3-q22.05 

Ehlers-Danlos syndrome, type VIIA2 (3) 7q21.3-q22.1 

?Ehlers-Danlos syndrome, type X (3) 2q34-q36 

[Elliptocytosis, Malaysian-Melanesian type] (1) 17q21-q22 

Elliptocytosis-1 (3) 1p36.2-p34 

Elliptocytosis-2 (2) 1q21 

Elliptocytosis-3 (2) 14q22-q23.2 

Emery-Dreifuss muscular dystrophy (2) Xq28 

Emphysema (1) 14q32.1 

Emphysema due to alpha-2-macroglobulin deficiency (1) 12p13.3-p12.3 

218

Emphysema-cirrhosis (1) 14q32.1 

Enolase deficiency (1) 1pter-p36.13 

?Eosinophilic myeloproliferative disorder (2) 12p13 

Epidermolysis bullosa dystrophica, recessive (3) 11q11-q23 

Epidermolysis bullosa Ogna type (2) 8q24 

Epidermolysis bullosa progressiva (2) Unassigned Link 

?Epidermolysis bullosa simplex, Koebner type 1q21-q24 

Epilepsy, juvenile myoclonic (2) 6p21.3 

Epilepsy, progressive myoclonic (2) 21q22.3 

?Erythremia (1) 7q21-q22 

Erythremias, alpha- (1) 16pter-p13.3 

Erythremias, beta- (1) 11p15.5 

Erythroblastosis fetalis (1) 1p36.2-p34 

Erythrokeratodermia variabilis (2) 1p36.2-p34 

*[Euthyroidal hyper- and hypothyroxinemia] (1) Xq21-q22 

Ewing Sarcoma (2) 22q12 

Exertional myoglobinuria due to deficiency of LDH-A (1) 11p15.4 

Fabry disease (3) Xq22 

Facioscapulohumeral muscular dystrophy (2) 4q34-qter 

Factor H deficiency (1) 1q32 

Factor V deficiency (1) 1q23 

Factor VII deficiency (1) 13q34 

Factor X deficiency (1) 13q34 

Factor XI deficiency (1) 4q35 

Factor XII deficiency (1) 5q33-qter 

Factor XIIIA deficiency 6p25-p24 

Factor XIIIB deficiency 1q31-q32.1 

?Familial Mediterranean fever (1) 9q32-q33 

?Fanconi anemia (1) 1q41-q42 

Fanconi anemia-1 (2) 20Q 

Favism (1) Xq28 

?Fetal alcohol syndrome (1) 12q24.2 

?Fetal hydantoin syndrome (1) 1p22-qter 

Fletcher factor deficiency (1) 4q35 

*Focal dermal hypoplasia (2) Xp22.31 

Fragile X syndrome/Martin-Bell syndrome (2) Xq27.3 

Friedreich ataxia (2) 9q13-q21.1 

Fructose Intolerance (1) 9q22 

?Fryns syndrome (2) 1q24-q31.2 

Fucosidosis (1) 1p34 

Fumarase deficiency (1) 1q42.1 

219

G6PD deficiency (1) Xq28 

Galactokinase deficiency (1) 17q21-q22 

Galactose epimerase deficiency (1) 1pter-p32 

Galactosemia (1) 9p13 

Galactosialidosis (1) 20q13.1 

Gardner syndrome (2) 5q22-q23 

Gaucher disease (1) 1q21 

Gerstmann-Straussler disease (2) 10q21-q22 

Glanzmann thrombasthenia, type A (1) 20pter-p12 

Glanzmann thrombasthenia, type B (1) 17q21.32 

Glaucoma, congenital (2) 17q21.1-q21.3 

Glioblastoma multiforme (2) Chr.11 

Glutaricaciduria, type II (1) 10p12-q23.2 

Glutaricaciduria, type IIc (1) 15q23-q25 

Glutathioninuria (1) Chr.19 

Glycerol kinase deficiency (2) 22q11.1-q11.2 

Glycogen storage disease VII (1) Xp21.3-p21.2 

*Glycogen storage disease, X-Linked hepatic (2) Xp22 

[Glyoxalase II deficiency] (1) 16p13 

GM1-Gangliosidosis (1) 3p21-p14.2 

GM2-Gangliosidosis, juvenile, adult (1) 15q22-q25.1 

GM2- Gangliosidosis, AB variant (1) Chr.5 

Goeminne TKCR syndrome (2) Xq28 

Goiter, adolescent multinodular (1) 8q24.2-q24.3 

?Goldenhar syndrome (2) 7p 

*Gonadal dysgenesis, XY female type F (2) Xp22-p21 

Gonadoblastoma (2) 11p13 

*?Gonadotropin deficiency (2) Xp21 

Granulomatous disease, autosomal, due to deficiency of CYBA 16q24 

Granulomatous disease, chronic, X-Linked (2) Xp21.1 

Greig craniopolysyndactyly syndrome (2) 7p13 

*?Growth hormone deficiency, X-Linked (2) Xq21.3-q22 

?Gynecomastia, familial, due to increased aromatase activity (1) 

Gyrate atrophy of choroids and retina with ornithinemia, B6 

15q21.1 

responsive or unresponsive (1) 10q26 

Harderoporphyria (1) Chr9 

Hb H mental retardation syndrome (2) 16pter-p13.3 

Heinz body anemias, alpha- (1) 16pter-p13.3 

Heinz body anemias, beta- (1) 11p15.5 

Hemochromatosis (2) 6p21.3 

Hemodialysis-related amyloidosis (1) 15q21-q22 

220

Hemolytic anemia due to ADA excess (1) 20q13.11 

Hemolytic anemia due to adenylate kinase deficiency (1) 9q34.1 

Hemolytic anemia due to bisphosphoglycerate mutase deficiency (1) 7q31-q34 

Hemolytic anemia due to G6PD deficiency (1) Xq28 

Hemolytic anemia due to glucosephosphate isomerase deficiency (1) 19cen-q12 

Hemolytic anemia due to glutathione peroxidase deficiency (1) 11-q12 

Hemolytic anemia due to glutathione reductase deficiency (1) 8p21.1 

Hemolytic anemia due to hexokinase deficiency (1) 10p11.2 

Hemolytic anemia due to PGK deficiency (1) Xq13 

Hemolytic anemia due to phosphofructokinase deficiency (1) 21q22.3 

Hemolytic anemia due to triosephosphate isomerase deficiency (1) 12p13 

Hemophilia A (3) Xq28 

Hemophilia B (3) Xq27.1-q27.2 

Hemorrhagic diathesis due to “antithrombin” Pittsburgh (1) 14q32.1 

Hemorrhagic diathesis due to PAI1 deficiency (1) 7q21.3-q22 

?Hepatic lipase deficiency (1) 15q21-q23 

?Hepatocarcinoma (2) 2q14-q21 

Hepatocellular carcinoma (3) 4q32.1 

[Hereditary persistence of alpha-fetoprotein] (3) 4q11-q13 

?Hereditary persistence of fetal hemoglobin (3) 11p15.5 

*[Hereditary persistence of fetal hemoglobin, Swiss type (2) Xp11.23 

Hers disease, or glycogen storage disease VI (1) Chr.14 

Heterocellular hereditary persistence of fetal hemoglobin (2) 11p15 

*?Heterocellular hereditary persistence of fetal hemoglobin (2) Xq28 

!Hex A pseudodeficiency! (1) 15q22-q25.1 

?H syndrome (2) 13q34 

[Histidinemia] (1) 12q22-q23 

?Holoprosencephaly (2) 2p21 

?Holoprosencephaly (2) 21q22.3 

?Holoprosencephaly (2) 7q36 

?Holt-Oram syndrome (2) 14q23-q24.2 

?Holt-Oram syndrome (2) 20p13 

Homocystinuria, B6-responsive and nonresponsive types (1) 21q22.3 

HPFH, deletion type (1) 11p15.5 

HPFH, nondeletion type A (1) 11p15.5 

HPFH, nondeletion type G (1) 11p15.5 

HPRT-related gout (1) Xq26-q27.2 

Huntington’s disease (2) 4p16.3 

Hurler syndrome (1) 4p16.3 

Hurler-Scheie syndrome (1) 4p16.3 

221

Hydrocephalus, X-Linked (2) Xq28 

Hydrops fetalis, 1 form (1) 19cen-q12 

Hyperammonemia due to CTPase deficiency (1) 1pter-q12 

Hyperbetalipoproteinemia (1) 2p24 

Hypercholesterolemia, familial (3) 19p13.2-p13.1 

?Hyperglycinemia, isolated nonketotic, type I (2) 9p22 

?Hypergonadotropic hypogonadism (1) 19q13.32 

?Hyperimmunoglobulin G1syndrome (2) 14q32.33 

Hyperkalemic periodic paralysi (3) 17q23.1-q25.3 

?Hyperleucinemia-isoleucinemia or hypervalinemia (1) 12pter-q12 

Hyperlipoproteinemia I (1) 8p22 

Hyperlipoproteinemia, type Ib (1) 19q13.1 

Hyperlipoproteinemia, type III (1) 19q13.1 

[Hyperphenylalaninemia, mild] (3) 12p24.1 

[?Hyperproglucagonemia] (1) 2q36-q37 

Hyperproinsulinemia, familial (1) 11p15.3 

Hypertriglyceridemia, 1 form (1) 11q23 

Hypertrophic cardiomyopathy, 1 form (3) 14q12 

?Hypervalinemia or hyperleucine-isoleucinemia (1) Chr.19 

Hypobetalipoproteinemia 11q23 

Hypobetalipoproteinemia (1) 2p24 

[Hypoceruloplasminemia, hereditary] (1) 3q21-q24 

Hypofibrinogenemia, gamma types (1) 4q28 

?Hypogonadotropic hypogonadism due to GNRH deficiency (1) 8p21-q11.2 

Hypomagnesemia, X-Linked primary (2) Xp22 

?Hypomelanosis of Ito (2) 15q11-q13 

?Hypomelanosis of Ito (2) 9q33-qter 

Hypoparathyroidism, familial (1) 11p15.3-p15.1 

*Hypoparathyroidism, X-Linked (2) Xq26-q27 

?Hypophosphatasia, adult (1) 1p36.1-p34 

Hypophosphatasia, infantile (3) 1p36.1-p34 

Hypophosphatemia, hereditary (2) Xp22.2-p22.1 

?Hypophosphatemia with deafness (2) Xp22 

Hypoprothrombinemia (1) 11p11-q12 

Hypothyroidism, hereditary congenital, 1 or more types (1) 8q24.224.3 

Hypothyroidism, nongoitrous (1) 1p22 

Hypothyroidism, nongoitrous, due to TSH resistance (1) 14q31 

?Ichthyosis vulgaris (1) 1q21 

Ichthyosis, X-Linked (3) Xpter-p22.32 

Immunodeficiency, X-Linked, with hyperIgM (2) Xq24-q27 

*Incontinentia pigmenti, familial (2) Xq27-q28 

222

Incontinentia pigmenti, sporadic type (2) Xp11.21 

Infertile male syndrome (1) Xcen-q13 

[Inosinie triphosphatase deficiency] (1) 20p 

Interferon, alpha, deficiency (1) 9p21 

Interferon, immune, deficiency (1) 12q24.1 

?Isolated growth hormone deficiency due to defect in GHRF (1) 20p11.23qter 

Isolated growth hormone deficiency, Illig type with absent GH and 

Kowarski type with bioinactive GH (3) 17q22-q24 

Isovalericacidemia (1) 15q14-q15 

?Jacobsen syndrome 11q 

Kallmann syndrome X22.3 

Kennedy disease (2) Xq21.3-q22 

?Kniest dysplasia (1) 12q13.11-q13.2 

?Kostmann agranulocytosis (2) 6p21.3 

Krabbe disease (1) 14q21-q31 

?Lactase deficiency, adult (1) Chr.2 

?Lactase deficiency, congenital (1) Chr.2 

?Lactoferrin-deficient neutrophils 3q21-q23 

Langer-Giedon syndrome (2) 8q24.11-q13.2 

Langer-Saldino achondrogenesis-hypochondrogenesis (1) 12q13.11-q13.2 

Laron dwarfism (1) 5p13-p12 

?Laryngeal adductor paralysis (2) 6p21.3—p21.2 

{Lead poisoning, susceptibility to} (1) 9q34 

?Leiomyomata, multiple hereditary cutaneous (2) 18p11.32 

Leprechaunism (1) 19p13.3-p13.2 

Lesch-Nyhan syndrome (3) Xq26-27.2 

?Letterer-Siwe disease (2) 13q14-q31 

Leukemia, acute lymphoblastic (1) 19p13.3.-p13.2 

?Leukemia, acute lymphocytic, with 4/11 translocation (3) 4q21 

Leukemia, acute myeloid, M2 type (1) Xpter-p21 

Leukemia, acute T-cell (2) 11p13 

Leukemia, chronic myeloid (3) 22q11.21 

Leukemia, chronic myeloid (3) 9q34.1 

Leukemia, T-cell acute lymphocytic (2) 10q24 

Leukemia/Lymphoma, B-cell, 1 (2) 11q13.3 

Leukemia/Lymphoma, B-cell, 2 (2) 18q21.3 

Leukemia/Lymphoma, B-cell, 3 (2) 19q13 

Leukemia/Lymphoma, T-cell, (2) 1p32 

Leukemia/Lymphoma, T-cell, (2) 14q32.1 

Leukemia/Lymphoma, T-cell, (2) 2q34 

Leukemia/Lymphoma, T-cell, (3) 14q11.2 

223

Leukocyte adhesion deficiency (2) 21q22.3 

Li-Fraumeni syndrome (1) 17p13.1 

Lipoamide dehydrogenase deficiency (1) 7q31-q32 

Lipoid adrenal hyperplasia, congenital (1) Chr.15 

Lipoma (2) 12q13-q14 

Liver cell carcinoma (1) 11p14-p13 

Long QT syndrome (2) 11p15.5 

Lowe’s syndrome Xq25 

Lupus erythematosus, systemic (1) 1q23-q24 

Lymphoproliferative syndrome, X-linked (2) Xq25 

?Lynch cancer family syndrome II (2) 18q11-q12 

?Lysosomal acid phosphatase deficiency (1) 11p12-p11 

Macrocytic anemia of 5q syndrome II (2) 5q12-q32 

Macular dystrophy, atypical vitelliform (2) 8q24 

Macular dystrophy,?vitelline type (2) 6p25-qter 

?Major mental illness (2) 11p21-q22 

?Male infertility due to acrosin deficiency (2) 22q13-qter 

?Male infertility, familial 11p13 

?Male pseudohermaphroditism due to defective LH (1) 19q13.32 

Malignant hyperthermia (2) 19q13.1-q13.3 

Malignant melanoma, cutaneous (2) 1p36 

Manic-depressive illness, X-Linked (2) Xq28 

Mannosidosis (1) 19p13.2-q12 

Maple syrup urine disease (1) 19q13.1-q13.2 

Maple syrup urine disease, type II (1) 1p31 

Maple syrup urine disease, type III (3) 6p22-p21 

Marfan syndrome (2) 15q-q21.3 

Maroteaux-Lamy syndrome (1) 5q11-q13 

Martin-Bell syndrome/Fragile X syndrome (2) Xq27.3 

NASA syndrome (2) Xq28 

McArdle disease (1) 11q13 

*[McLeod phenotype] (2) Xp21.2-p21.1 

Medullary thyroid carcinoma (2) 10q21.1 

?Megacolon (2) 13q22.1-q32.1 

?Megaloblastic anemia 5q11.1-q13.2 

?Megalocomea, X-Linked (2) Xq21.3-q22 

Meningioma (2) 22q12.3-qter 

Meningioma (3) 22q12.3-q13.1 

Menkes disease (2) Xq12-q13 

Mental retardation of WAGR (2) 11p13 

*Mental retardation, X-Linked nonspecific, I (2) Xp22 

224

*Mental retardation, X-Linked nonspecific, II (2) Xq11-q12 

*Mental retardation-skeletal dysplasia (2) Xq28 

Metachromatic Leukodystrophy (1) 22q13.31-qter 

Metachromatic Leukodystrophy due to deficiency of SAP-1 (1) 16pter-p13.3 

Methemoglobinemia, enzymopathic (1) 11p15.5 

Methylmalonicaciduria, mutase deficiency type (1) 6p21 

?Microcephaly, true (2) 1q31-q32.1 

Miller-Dieker Lissencephaly syndrome (2) 17p13.3 

MODY, 1 form (3) 11p15.5 

Mucolipidosis II (1) 4q21-q23 

Mucolipidosis III (1) 4q21-q23 

Mucopolysaccharidosis I (1) 4p16.3 

*Mucopolysaccharidosis II (2) Xq28.1 

Mucopolysaccharidosis IVB (1) 3p21-p14.2 

Mucopolysaccharidosis VII (1) 7q22 

Multiple endocrine neoplasia II (2) 11q13 

Multiple endocrine neoplasia II (2) 10q21.1 

Multiple endocrine neoplasia III (2) 10q21.1 

?Multiple exostoses (2) 8q23-q24.1 

?Multiple Lipomatosis (2) 12q13-q14 

?Muscle glycogenosis (1) Xq12-q13 

Myeloperoxidase deficiency (1) 17q21.3-q23 

Myoadenylate deaminase deficiency (1) 1p21-p13 

Myopathy due to CTPase deficiency (1) 1pter-q12 

Myopathy due to phosphoglycerate mutase deficiency 7p13-p12.3 

Myotonic dystrophy (2) 19q13.2-q13.3 

Myotubular myopathy, X-Linked (2) Xq28 

Myxoid Liposarcoma (2) 12q13-q14 

*?N syndrome Xp23.3-p21.1 

Nail-patella syndrome (2) 9q34 

*Nance-Horan syndrome (2) Xp22.3-p21.1 

Neuroblastoma (2) 1p32 

Neuroepithelioma (2) 22q12 

Neurofibromatosis, von Recklinghausen (2) 17q11.2 

Neutropenia, immune (2) 1q23-q24 

?Nevoid basal cell carcinoma syndrome (2) 1p 

Niemann-Pick disease (1) 11p15.4-15.1 

*Nightblindness, congenital stationary, type I (2) Xp11.3 

Norrie’s disease (2) Xp11.4 

Norum disease (3) 16q22.1 

Nucleoside phosphorylase deficiency, immunodeficiency due to (2) 14q13.1 

225

*Ocular albinism, Forsius-Eriksson type (2) Xp11-q11 

Ocular albinism, Nettleship-Falls type (2) Xp22.3 

?Optic atrophy, Kjer type (2) 2p 

Ornithine transcarbamylase deficiency (3) Xp21.1 

Orofacial cleft (2) 6pter-p23 

Oroticaciduria (1) 3q13 

Osteoartrosis, precocious (3) 12q13.11-q13.2 

Osteogenesis imperfecta, 2 or more clinical forms (3) 17q21.31-q22.05 

Osteogenesis, retinoblastoma-related (2) 7q21.3-q22.1 

Osteosarcoma, retinoblastoma-related (2) 13q14.1 

Ovarian carcinoma (2) 9p24 

*Ovarian failure, premature (2) Xq26-q27 

Oxalosis I (1) 2q36-q37 

?Paget disease of bone (2) 6p21.3 

{?Parkinsonism, susceptibility to} (1) 22q11.2q12.2 

Paroxysmal nocturnal hemoglobinuria (1) 11p14-p13 

Pelizaeus-Merzbacher disease (3) Xq22 

?Pendred syndrome (2) 8q24 

Periodontitis, juvenile (2) 4q11-q13 

Persistent Mullerian duct syndrome (1) 19p13.3-p13.2 

Phenylketonuria (3) 12q24.1 

Phenylketonuria due to dihydropteridine reductase deficiency (1) 4p15.31 

*Phosphoribosylpyrophosphate synthetase-related gout (1) Xq22-q24 

?Phosphorylase kinase deficiency of liver and muscle (2) 16q12-q13.1 

?Piebaldism (2) 4q12 

PK deficiency hemolytic anemia (1) 1q21-q22 

[Placental lactogen deficiency] (1) 17q22-q24 

Placental steroid sulfatase deficiency (3) Xpter-p22.32 

Plasmin inhibitor deficiency (1) 18p11.1-q112 

Plasminogen activator deficiency (1) 8p12 

Plasminogen deficiency, types I and II (1) 6q26-q27 

Plasminogen Tochigi disease (1) 6q26-q27 

Platelet alpha/delta storage pool deficiency (1) 1q21-q24 

{Polio, susceptibility to} (2) 19q12-q13.2 

Polycystic kidney disease (2) 16p13.31-p13.12 

Polycystic ovarian disease (1) 17q11-q12 

Polyposis coli, familial (2) 5q22-q23 

Pompe disease (1) 17q23 

Porphyria, acute hepatic (1) 9q34 

Porphyria, acute intermittent (1) 11q23.2-qter 

Porphyria, congenital erythropoietic (1) 10q25.2-q26.3 

226

Porphyria, cutanea tarda (1) 1p34 

Porphyria, hepatoerythropoietic (1) 1p34 

Porphyria variegata (2) 14q32 

Postanesthetic apnea (1) 3q25.2 

Prader-Willi syndrome (2) 15q11 

*Progressive cone dystrophy (2) p21.1-p11.3 

Prolidase deficiency (1) 19cen-q13.11 

*Properdin deficiency, X-Linked (3) Xp11.4 

Propionicacidemia, type I or pccA type (1) 13q32 

Propionicacidemia, type II or pccB type (1) 3q13.3-q22 

Protein C deficiency (1) 2q13-q14 

Protein S deficiency (1) 3p11.1-q11.2 

Pseudohermaphroditism, male, with gynecomastia (1) 17q11-q12 

Pseudohypoaldosteronism (1) 4q31.1 

Pseudohypoparathyroidism, type Ia (1) 2oq13.2-q13.3 

Pseudo-Zellweger syndrome (1) 3p23-p22 

?Pyridoxine dependency with seizures (1) 2q 

Pyropoikilocytosis (1) 1q21 

Pyruvate carboxylase deficiency (1) 11q 

*Pyruvate dehydrogenase deficiency (1) Xp22.2-p22.1 

?Rabson-Mendenhall syndrome (1) 19p13.3-p13.2 

?Ragweed sensitivity (2) 6p21.3 

Reifenstein syndrome (1) Xcen-q13 

Renal cell carcinoma (2) 3p14.2 

[Renal glucosuria] (2) 6p21.3 

?Retinal cone dystrophy-1 (2) 6p25-q25 

?Retinal cone-rod dystrophy (2) 18q21-q22.2 

Retinitis pigmentosa, autosomal dominant (3) 3q21-q24 

Retinitis pigmentosa-2 (2) Xp11.3 

Retinitis pigmentosa-3 (2) Xp21.3 

Retinoblastoma (2) 13q14.1-q14.2 

?Retinol binding protein, deficiency of (1) 10q23-q24 

Retinoschisis (2) Xp22.3-p22.1 

*?Rett syndrome (2) Xp 

Rhabdomyosarcoma (2) 11p15.5 

Rhabdomyosarcoma, alveolar (2) 2q37 

Rh-null disease (1) 3cen-q22 

?Rh-null hemolytic anemia (1) 1p36.2-p34 

Rieger syndrome (2) 4q23-q27 

?Rothmund-Thomson syndrome (2) Chr.18 

Salivary gland pleomorphic adenoma (2) 8q12 

227

Sandhoff disease (1) 5q13 

Sanfilippo syndrome D (1) 12q14 

*Sarcoma, synovial (2) Xp11.2 

Scheie syndrome (1) 4p16.3 

*SCID, X-Linked (2) Xq13.1-q21.1 

Sclerotylosis (2) 4q28-q31 

Seizures, benign neonatal (2) Chr.20 

Severe combined immunodeficiency due to ADA deficiency (1) 20q13.11 

Severe combined immunodeficiency due to IL-2 deficiency (1) 4q26-q27 

Severe combined immunodeficiency (SCID), HLA class II-negative type (1) 19p13 

?Sialidosis (1) Chr.10 

?Sialidosis (2) 6p21.3 

Sicle cell anemia (1) 11p15.5 

?Situs inversus viscerum (2) 14q32 

?SLE (1) 1q32 

Small-cell cancer of lung (2) 3p23-p21 

?Smith-Lemli-Opitz syndrome (2) 7q23-qter 

Smith-Magenis syndrome (2) 17p11.2 

Spastic paraplegia, X-Linked, uncomplicated (2) Xq21-q22 

Spherocytosis, recessive (1) 1q21 

Spherocytosis-1 (3) 14q22-q23.2 

Spherocytosis-2 (3) 8p11.2 

Spinal muscular atrophy II (2) 5q11.2-q13.3 

Spinal muscular atrophy III (2) 5q11.2-q13.3 

Spinocerebellar-ataxia 6p21.3-p21.2 

Spondyloepiphyseal dysplasia congenital (3) 12q13.11-q13.2 

*Spondyloepiphyseal dysplasia tarda (2) Xp22 

Stickler syndrome (3) 12q13.11-q13.2 

Sucrose intolerance (1) 3q25-q26 

?Susceptibility to amyloid in FMF (1) 11pter-p12 

Tay-Sachs disease (1) 15q22-q25.1 

Testicular feminization (1) Xcen-q13 

Thalassemias, alpha- (1) 16pter-p13.3 

Thalassemias, beta- (1) 11p15.5 

Thrombocytopenia, X-Linked (2) Xp21-p11 

Thrombophilia due to elevated HRG (2) 3p14-qter 

Thrombophilia due to excessive plasminogen activator inhibitor (1) 7q21.3-q22 

Thrombophilia due to heparin cofactor II deficiency (1) Chr.22 

Thyroid hormone resistance (3) 3p24.3 

Thyroid iodine peroxidase deficiency (1) 2pter-p12 

Thyroid papillary carcinoma (1) 10q11-q12 

228

Thyrotropin-releasing hormone deficiency (2) Chr.3 

Torsion dystonia (2) 9q32-q34 

Torsion dystonia-parkinsonism, Filipino type (2) Xq21 

?Tourette syndrome (2) 18q22.1 

Transcobalamin II deficiency (1) 22q11.2-qter 

[Transcortin deficiency](1) 14q31-q32.1 

?Treacher Collins mandibulofacial dysostosis 5q11 

Trichorhinophalangeal syndrome, type I (2) 8q24.2 

Trypsinogen deficiency (1) 7q32-qter 

Tuberous sclerosis-1 (2) 9q33-q34 

Tuberous sclerosis-2 (2) 11q23 

Tyrosinemia, type I (1) 15q23-q25 

Tyrosinemia, type II (1) 16q22.1-q22.3 

Urolithiasis, 2,8-dihydroxyadenine (1) 16q24 

Usher syndrome, type-2 (2) 1q32 

van der Woude syndrome (2) 1q32 

Vitamin D dependency, type I (2) 12q14 

{Vivax malaria, susceptibility to} (1) 1q21-q22 

von Hippel-Lindau syndrome (2) 3p26-p25 

von Willebrand disease (1) 12pter-p12 

Waardenburg syndrome, type I (2) 2q37.3 

?Watson syndrome (2) 17q11.2 

Werdnig-Hoffmann disease (2) 5q11.2-q13.3 

*Wieacker-Wolff syndrome (2) Xq13-q21 

Wilms tumor (2) 11p13 

Wilms tumor, type 2 (2) 11p15.5 

Wilson disease (2) 13q14-q21 

Wiskott-Aldrich syndrome (2) Xp11.3-p11.2 

Wolf-Hirschhorn syndrome (3) 4p16.1 

Wolman disease (1) 10q24-q25 

?Xeroderma pigmentosum (1) 1q41-q42 

?Xeroderma pigmentosum, 1 form (1) 19q13.2-q13.3 

Xeroderma pigmentosum, group A (1) 9q34.1 

Xeroderma pigmentosum, group B (1) 2q21 

Xeroderma pigmentosum, group F (2) Chr.15 

?Xeroderma pigmentosum, one type (1) Chr.13 

Zellweger syndrome (2) 7q11.23 

229

Chromosome 

No. 

DR. RECOMMENDS METABOLIC 1 

A CHROMOSOME HOMEOPATHIC 

RNA Control 13 Nerval Disease 

1A RNA Control 13A Nerval Disease 

2 RNA Control 14 Nerval Disease 

2A RNA Control (Tactile) 14A Nerval Disease 

3 RNA Control (Vision) 15 Nerval Disease 

3A RNA Control (Hearing) 15A Nerval Disease 

4 RNA Control 16 MS 

4A RNA Control 16A MD 

5 RNA Control 17 Digestive 

5A RNA Control 17A Kidney Problems 

6 Bone Disturbance 18 Kidney Problems 

6A Bone Disturbance 18A Kidney Problems 

7 Skin Disturbance 19 Liver Problems 

7A Skin Disturbance 19A Liver Problems 

8 Lipid Metabolism 20 Liver Problems 

8A Cholesterol Control 20A Pancreas 

9 Cholesterol Control 21 Pancreas 

9A Cholesterol Control 21A Pancreas 

10 Blood Disturbance 22 Brain 

10A Blood Disturbance 22A Brain 

11 Downs Syndrome (Alzheimers) 23 Sex System 

11A Downs Syndrome (Alzheimers) 23A Addiction 

12 Immune System 24 Extra Chromosome (Sociopath) 

12A Immune System 

230

LECTINS 

Lectins are proteins or glycoproteins of non-immune origin that 

agglutinate cells and/or precipitate complex carbohydrates. The 

agglutination activity of these highly specific carbohydrate-binding 

molecules is usually inhibited by a simple monosaccharide, but for some 

lectins di, tri, and even polysaccharides are required. 

Lectins are isolated from a wide variety of natural sources, including 

seeds, plant roots and bark, fungi, bacteria, seaweed and sponges, 

mollusks, fish eggs, body fluids of invertebrates and lower vertebrates 

and from mammalian cell membranes. The precise physiological role of 

lectins in nature is still unknown, but they have proved to be very 

valuable in a wide variety of applications in vitro, including: 

� Blood groupings and erythrocyte poly agglutination studies 

� Mitogenic stimulation of lymphocytes 

� Lymphocyte subpopulation studies 

� Fractionation of cells and other particles 

� Isolation, purification and structural studies of carbohydrate 

containing molecules 

� Histochemical studies of normal and pathological conditions 

Source: http://www.answers.com/topic/lectin?cat=health / 

http://books.google.com/books?id=9xWhUBTdDqgC&pg=PA30&lpg=PA30&dq=lectins 

+are+proteins+or+glycoproteins+of+%22non+immune%22+origin+that+agglutinate+cell 

s&source=web&ots=5zlpr6hyyU&sig=nCH_vu506zeDKX5XEuwc_LyXXgQ 

231

Asparagus Pea 

Avocado 

Black Locust 

Broad Bean 

Camels Foot Tree 

Chick Pea 

Concanavalin A 

Coral Tree (Israel) 

Eel 

Elder 

False Acacia 

Fava Bean 

Furze 

Gorse 

Green Marine Algae 

Hairy Vetch 

Horse Gram 

Horseshoe Crab 

Jack Bean 

Japanese Wisteria 

Jimson Weed 

Laburnum, Scotch 

Lentil 

Lima Bean 

Common Name 

232 

Limulin 

Mung Bean 

Mushroom 

Osage Orange 

Pagoda Tree 

Pea, Garden 

Peanut 

Pokeweed 

Potato 

Red Kidney Bean 

Red Marine Algae 

Roman Snail 

Scarlet Runner Bean 

Siberian Pea Tree 

Snail, Garden 

Soybean 

Spindle Tree 

Sweet Pea 

Thorn Apple 

Tomato 

Wheat Germ 

Winged Bean 

Winged Pea

OLIGO ELEMENTS 

FIRE DIATHESIS III 

Manganese-Cobalt 

EARTH DIATHESIS V 

Zinc-Nickel-Cobalt, Zinc-Copper 

METAL DIATHESIS II 

Manganese-Copper 

WATER DIATHESIS IV 

Copper-Gold-Silver 

WOOD DIATHESIS I 

Manganese 

IODINE 

LITHIUM 

MAGNESIUM 

SULPHUR 

ZINC 

OLIGO DEOXYRIBONUCLEOTIDE 

URACIL 

CYTOSINE 

ADENINE 

THYMINE 

INOSINE 

GUANINE 

233

MINERALS 

ALUMINUM 

BORON 

CALCIUM 

CARBON 

CHLORINE 

CHROMIUM 

BOCALT 

COPPER 

HYDROGEN 

IODINE 

IRON 

MAGNESIUM 

MANGANESE 

MOLYBDENUM 

NICKEL 

NITROGEN 

OXYGEN 

PHOSPHOROUS 

POTASSIUM 

SELENIUM 

SILICON 

SODIUM 

SULPHER 

TIN 

VANADIUM 

ZINC 

234

235 

METALLIC ELEMENTS 

ALUMINUM 

AMERICUM 

ANTIMONY 

ARGON 

ARSENIC 

BARIUM 

BERYLLIUM 

BISMUTH 

BROMINE 

CADMIUM 

CALCIUM 

CERIUM 

CESIUM 

CHROMIUM 

COBALT 

COPPER 

FLOURINE 

GALANIUM 

GALLIUM 

GERMANIUM 

GOLD 

HAFNIUM 

HELIUM 

IODINE 

IRIDIUM 

IRON 

KRYPTON 

LANTHANUM 

LEAD 

LITHIUM 

MAGNESIUM 

MANGANESE 

MENDELEVIUM 

MERCURY 

MOLYB 

NEODYMIUM 

NEON 

NIOBIUM 

OSMIUM 

PLATINUM 

PLUTONIUM 

POLONIUM 

POTASSIUM 

RADIUM 

RADON 

RUBIDIUM 

SB 

SCANADIUM 

SELENIUM 

SILVER 

SODIUM 

STRONTIUM 

TECHNETIUM 

TELLURIUM 

THORIUM 

TIN 

TITANIUM 

TUNGSTEN 

URANIUM 

VANADIUM 

W 

XENON 

YTTRIUM 

ZINC 

ZIRCONIUM

PHENOLICS 

Acetaldehyde: Petrochemical sensitivity, (perfumes, flavors, dyes, 

plastics, synthetic rubber), alcoholism, spreading phenomenon of 

allergies to foods, sugar, metabolism, and yeast. 

Acetylcholine Chloride: Parasympathetic stimulant (neurotransmitter) 

lowers blood pressure; chronic fatigue, depression, phobias, 

schizophrenia. 

Apiol: PHS, obesity, infertility, gout, arthritis, hypothalamus-pituitary 

axis, homosexuals. 

Ascorbic Acid: Allergic shiners, antioxidant, anxiety, bleeding gums and 

gum disease, cataracts, chemical sensitivity, collagen disease, dental 

caries, diarrhea, easy bruising, edema, fatigue, frequent infections, fruit 

intolerance, high cholesterol level, hyperactivity, hypertension, light 

sensitivity, loss of appetite, mental problems, muscle soreness, open 

angle glaucoma, premature aging, slow wound healing, stiff and tender 

joints, weakness in connective tissue. 

Butylatedhydroxytoluene (BHT): Aggression, belligerence, depression, 

hyperactivity, temper outbursts. 

Caffeic Acid: Constricts capillary walls, stimulates ACTH release 

(decreasing thymus weight), allergic rhinitis, pharyngeal drainage, otitis, 

asthma. 

Chlorogenic Acid: Allergies to pollens, dust, molds; skin rashes, 

congestion and headaches, asthma, hay fever. 

Cinnamic Acid: Bladder dysfunction, cystitis, enuresis, skin problems, 

(acne, eczema, psoriasis), congestion, asthma, chronic fatigue, 

hypoglycemia, cravings for fruit. 

Coniferyl Alcohol: Allergies to evergreens, headaches. 

Coumarin: Constricts capillary walls, inhibits clotting, estrogen effect 

asthma, hay fever, digestive problems, low back and cervical neck pain, 

chronic fatigue. 

Dopamine: Neurotransmitter, arrhythmia, Parkinsonism, anxiety, 

depression, dyslexia, autism, schizophrenia. 

Estrogen: PMS, cyclic changes, (closely associated with Vitamin D), 

effeminate traits in males. 

236

PHENOLICS, cont. 

Gaba: Lowers blood pressure, inhibitory transmitter in brain, anger, 

hostility. 

Gallic Acid: Related to racing heart, anti-cancer (in 80% foods-universal 

reactor), chronic sinusitis, rhinitis, craving sweets, musculo-skeletal 

problems (low back pain), chronic fatigue, hyper-activity. 

Histamine: Released from injured cells, increases pore size, dilates 

capillaries, hay fever, vertigo. 

Indole: Bloating, constipation, asthma, allergic rhinitis, sinus 

congestion, chronic fatigue, common in milk drinkers and children. 

L-Dopa: Arrhythmia, stimulates ACTH release (decreasing thymus 

weight), Parkinsonism, chronic anxiety, depression. 

Malvin: Red to purple coloring in food, arthritis, psoriasis, asthma, 

epilepsy, MS, dyslexia, autism, hyperactivity. 

Mannan: Constitutes 30-50% of yeast cell wall, suppresses T-lymphocyte 

production, chronic hives, angio-edema. 

Menadione: Related to Vitamin K production, liver dysfunction, fatigue, 

easy bruising, chronic nosebleeds, chronic colitis, diarrhea, varicose 

veins, arthritis. 

Norepinephrine: Stimulates sympathetic nervous system (fight or flight), 

raises blood pressure, maintains freedom from depression, agoraphobia. 

Octopamine: Petrochemical sensitivities. 

Phenylalanine: Building block for dopamine, cinnamic acid, caffeic acid, 

coumarin and coniferyl alcohol, headaches, blurred vision, poor appetite, 

depression, sleep disorders. 

Phenylisothiocyanate: MD, diarrhea, chronic arrhythmia, hypertension, 

thyroid dysfunction. 

Phloridzin: Strengthens vascular system, blocks absorption of glucose in 

kidneys (glucosuria), sugar cravings, collagen diseases. 

Piperine: Stomach disorders. 

237

Progesterone: PMS, menopausal stress, temporarily raises cholesterol 

levels. 

Pyrole: Gas, bloating, anxiety, depression, mauve factor in 

schizophrenia. 

Quercetin: In 78% of foods. Hay fever, suppresses histamine release, 

chelates with metals to prevent oxidation of Vitamin C and adrenaline, 

decreases vascular fragility, stimulates adrenaline release, decreasing 

thymus weight, reduces overall metabolism, reduces temperature and 

oxygen consumption, suppresses thyroid activity, linked with male 

impotence. 

Rutin: Increases vascular strength, hay fever, rhinitis, reduces 

permeability of capillary walls. 

Salsolinol: Alcoholism, chocoholism, headaches, throat discomfort, 

general weakness, mental fog, obsessive-compulsive behavior. 

Serotonin: Neurotransmitter, sensory perception, temperature 

regulation, decreases bleeding, increases peristaltic motion, insomnia, 

memory loss, depression, dyslexia, mental retardation, obsessive, 

compulsive, aggressive, suicidal (lower serotonin level, higher aggression, 

and more violent suicide). 

Taurine: Stimulates liver function and bile flow, related to viruses in 

liver and environmental toxicity. 

Tryptophan: Antidepressant, sleep disorders, bloating, constipation, 

increases peristalsis, decreases bleeding, skin inflammations. 

Phenylpropanolamine: Aids in the elimination of environmental 

sensitivities. 

238

VENOMS 

Many different types of venom have been used historically in different 

medicines by many cultures. Snake venom in particular has gotten much 

attention throughout the ages. The snake was thought to represent death 

but also to represent aspects of life. It has been part of mythology in 

almost every culture. 

The symbol for healing, the staff with the snake around it, is used by 

the American Medical Association as its signature. Many aspects of 

healing are connected to snakes. 

Venoms were found to have many different effects for both medicine 

and biology. As early as 1737, Geoffroy and Hunault observed that the 

blood from cats and dogs bitten by vipers did not coagulate. In 1787, 

Felice Fontana found that when he injected a rabbit in the jugular vein 

with a small quantity of the same venom, this caused immediate death. 

On opening the vessels he found that the blood was coagulated. 

This was later solved in 1899, by M. Phisalix, who found that there 

were two distinct types of activity in this viper venom. One was an anti- 

coagulant at high doses, and the other a coagulant at low doses. This 

was part of the first evidence that some compounds could have various 

effects at different potencies. The amount of dilution could sometimes 

accomplish an influx or a distinct difference of action in potencies or 

dilutions. This was later developed as the Arndt-Schultz law of 

pharmacology which states that what a poison does at a raw dose, a 

dilute form of that poison will affect inversely, or paradoxically. 

Dr. Isaacs remarks that the effect between alpha receptors and beta 

receptors in the body is not a factor of different compounds that 

stimulate results, but different amounts of the same compound. Different 

dilutions can have different effects on neural transmitter points within 

the body which is key to the understanding of homeopathy, especially 

when looking at different snake and insect venoms. 

239

In 1854, Brainard found that venom in blood taken from animals 

bitten by crotalidae did not cause coagulation. In 1860, Mitchell found 

that the toxic secretion of the Crotalus adamanteus prevented blood from 

clotting in vitro. In 1893, Martin cited that the venom of elapidae (an 

example of which is the Pseudechis porphyriacus and the Notechis 

scutatus) coagulated blood in the vessels when injected at high doses; 

but at low doses it rendered the blood unable to coagulate. The venom of 

an Indian cobra when tested at any dose was found to inhibit blood 

coagulation in vivo and in vitro. This was found to be true in 1895, by D. 

D. Cunningham, in 1898, by Stephens and Meyers, in 1904, by Rogers. 

In 1901, George Lamb classified a dissertation of venoms according to 

their action on plasma. He noted in his article that Russell’s pit viper 

venom coagulated citrated plasma. This plasma does not in itself 

spontaneously coagulate. F. Noc confirmed these findings, and 

discovered that the venom of Asian and African elepidae prevented the 

coagulation of citrated plasma to which calcium chloride had been added 

for protection. 

In 1904, Paul Morawitz proposed that there was an essential element 

of the transformation of fibrinogen to fibrin which allows for the 

formation of different blood clots. The serozyme of serum acting on the 

cytozyme from the platelets caused thrombin to form. Thrombin was 

found to be the factor reacting on fibrinogen. 

In 1910, Noc presumed that some venom induced coagulation by the 

contribution of active thrombin to the blood. J. Mellanby found that 

coagulation of these venoms was increased by the addition of calcium. 

In 1912, Maurice Arthus put forth the idea that crotalidae acted as if it 

contained thrombin, whereas Russell’s pit viper venom accelerated the 

transformation of prothrombin to thrombin. 

In 1905, C. J. Martin was able to demonstrate that the coagulating 

factors of venoms did not pass through dialysis membranes. 

240

In 1904, Paul Morawitz introduced the idea of the enzyme capacities of 

these different venoms, and their ability to act very similarly to the 

digestive juices. 

The capacity of these venoms to have enzymatic action in the body was 

then determined. These venoms could be deadly if the enzyme activity 

was too intense such as in the case of Russell’s pit viper which causes 

thrombosis. 

Cortalus was a very strong enzyme; whereas elapidae was found to be 

weak proteolytically, but strong in its other enzyme activity. 

In 1912, C. Delezenne claimed that the venom of Lachesis contained 

akinase which activated pancreatic juice. Later in 1919, he observed in 

experiments that the toxic secretion of snakes was able to cause catalytic 

breakdown of nucleic acids. 

By the beginning of the twentieth century, classification of the different 

distinguishing properties of snake venoms was possible. Some acted as if 

they had ferments, or protein enzyme-like substances. Some were toxic. 

Some had diastases. 

In 1887, Henry Seawall, at the University of Michigan, Ann Arbor, was 

the first one in the United States to observe that a type of venom serum 

could be developed. He injected pigeons with small amounts of venom; 

not enough to cause death. Weeks later, the same pigeons, when injected 

with a larger quantity of the venom were able to resist the venom’s 

effects. 

Hahneman’s work with some snake venoms pointed out their reversal 

functions. This brief document is an attempt to discuss some of these 

venoms and their use in medicine today. 

Snakes can use their venom in many different ways. Often, the 

purpose of venom is to hunt and digest. People bitten by a snake usually 

have respiratory, circulatory, neurological, cardiac and coagulation 

problems. The enzymes in the venom will start digestion of the tissues of 

241

the victim so that the digestive system of the snake, which is not 

extremely strong, can get a head start on the digestive process. 

These venoms have strong pharmacological activity with a highly 

specific mode of action. Most of the contents of these venoms are 

proteins. Low molecular weight compounds such as peptides, nucleotides 

and metal ion are also often present. 

CLASSICS OF NEUROTOXINS 

In the neurotoxin development there are two pharmacological classes 

of neurotoxins: 1) those which are post-synaptic, and 2) those which are 

pre-synaptic. Curare is an example of a post-synaptic neurotoxin. It 

binds to the nicotinic acetylcholine receptors, and prevents the 

depolarizing action of acetylcholine. These toxins are usually referred to 

as curare-like toxins. Pre-synaptic toxins inhibit the release of 

acetylcholine, and their toxicity is much higher than that of the post- 

synaptic toxins. 

Another type of toxin is the membrane toxins which change the 

permeability of the membrane. They are often cardio-toxins, lytic factors, 

cytotoxins, etc. These names indicate the types of membranes they affect. 

Membrane toxins have been isolated only from elapid venoms. These 

membrane toxins work by penetrating into the hydrophobic layer of the 

membrane. Many of these toxins have phospholipase types of structures. 

A secondary hypothesis is that the membrane might be disrupted by the 

interaction of the disulfides in the toxin and the sulpha-hydro groups in 

the membrane. These toxin-induced permeability changes can have 

many biochemical and pharmacological activities. They might be 

hemolytic which would allow for the disruption of red blood cells; or 

cytotoxic, where they might induce a type of leukemia or lymphocytoma. 

There is a depolarizing effect of the different membranes which can cause 

peripheral nerve problems, contracture, paralysis, ventricular fibrillation 

242

and systolic arrest of the heart muscle. They might interfere with 

transport mechanisms such as inhibition of the accumulation of anions, 

amino acids, or glucose into the tissues of thyroid, kidney, small 

intestine, etc. There can be effects on membrane activity and membrane 

enzymes. This might provide inactivation of magnesium, sodium, 

potassium, and possibly even ATPase. All of these require intact 

membranes in order to function properly. Certain of these toxins can 

liberate calcium from muscle fibers and produce tetany. 

Some plants share some of these membrane toxins. An example is 

mistletoe which is a parasitic plant of the family Loranthaceae. Mistletoe 

toxins are very basic, and they have an isoelectric point of about pH11. 

They are very stable, and heating an ocular solution to 100 °C for thirty 

minutes has no influence on their toxicity. This mistletoe toxin consists 

of 46 amino acids in the peptide chain, cross-linked by three disulfides. 

These toxins in low concentration of ten micrograms per milliliter will 

produce depolarization and contraction in rabbit papillary and frog 

skeletal muscles, and the effects can be reversed by calcium. So it is 

suggested that the toxins bind to the cell membrane, and thus displace 

calcium. 

Let us proceed to analyze some of the different toxins provided by 

different venoms. One is crotoxin which is the main neurotoxin of the 

South American rattlesnake Crotalus durissus terrificus. This is a very 

powerful toxin which affects certain neurons and muscular structure. 

Specifically, the toxin from this snake produces problems in the neck 

and can contribute to nuchal rigidity. This has caused the South 

American rattlesnake to be called the “neck breaker,” because of its effect 

on neck muscles. Homeopathic crotoxin has been used quite successfully 

on neck and cervical conditions. 

The Australian tiapan, Oxyuranus scutellatus has extremely potent 

venom. It exhibits a low phospholipase activity, and has an effect similar 

243

to curare. The Australian tiger snake venom has strong effects in being 

able to bind calcium, and it is inactivated in the presence of bromine. 

Enhydrina schistosa, known as the common sea snake, has venom 

which produces myoglobinuria and muscle movement pains. Mice die 

rapidly of respiratory failure at high doses; whereas, at low doses, 

respiratory conditions can be treated. 

The venom of the Bungarus multicinctus has three different neurotoxic 

reactions, all of which produce a post-synaptic type of neuromuscular 

block. This bungaro toxin has a huge ability to inhibit choline uptake in 

the synaptic cleft, blocking the synthesis of acetylcholine which leads one 

to believe that it could be important in the homeopathic treatment of 

cholinergic diseases such as Alzheimer’s. 

The venom of different rattlesnakes contains a convulxin which 

induces convulsions in the intended victim. An example of a cardiotoxin 

comes from the Mohave rattlesnake venom. A compound known as 

Mohave is known to have dramatic cardiological effects. It is thought that 

this venom is also a phospholipase type of toxin. 

All types of Crotalus, especially the western diamond back rattlesnake, 

contain myocardial depressor proteins which suppress and produce a 

myocardial anesthesia or a myocardial depression in the animal. 

Some of the different rattlesnakes have a potent hypotensive peptide 

known as hypotensin which can dramatically reduce arterial pressure. 

Another interesting compound often found in snake venoms is that of 

NGF (nerve growth factor). NGF is an agent which regulates growth and 

differentiation of neurons in the sympathetic and in some cases sensory 

neural tissue. There are three principal characteristics of NGF: 1) the 

holofiber outgrowth from dorsal root or sympathetic ganglia; 2) the 

sympathetic ganglion enlargement in neonatal mice characterized by 

hyperplasia and hypertrophy; and 3) the immuno-sympathectomy, the 

destruction of sympathetic chain ganglia by the in vivo injection of anti- 

serum to NGF. 

244

Snake Venoms Containing NGF 

Oftentimes, this nerve growth factor occurs in the cobra family. Cobra 

venom seems to contain the highest amount of NGF of all the snake 

venoms. 

Viperidae Bothrops jararaca 

Bitis gabonica Crotalus adamanteus 

Echis carinatus Crotalus atrox 

Echis coloatus Crotalus horridus 

Vipera ammodytes Crotalus terrificus 

Vipera aspis Elapidae 

Vipera russellii Dendroaspis viridis 

Crotalidae Naja melanoleuca 

Agkistrodon piscivorus Naja naja 

Ancistrodon contortrix 

lactocinctus 

Naja nigrocollis 

Ancistrodon rhodostoma Sepedon haemachatus 

The venom of the Black Mamba, Dendroaspiaspsis jamesoni, causes 

marked depolarization of membranes and inhibits the excitability of 

skeletal muscles. This can effect cardiac and respiratory function; 

whereas, the cobra venom is primarily neuro-toxic and causes 

degenerative tissue to form. The venom of the families of the viper and 

rattlesnake are primarily related to hemorrhages and coagulation 

disturbances. The enzyme effect of these different venoms can start lysis 

in red cells as well as other cells of the body. This is to prepare the 

intended victim for digestion. Cobra venom lowers the red blood cell 

count in victims, but this alone does not seem to produce lethal effects. 

The most powerful hemolytic snake is the Pseudechis papuans, also 

known as the Papuan black snake. People bitten by this snake often 

produce red or black urine which results from the breakup of red blood 

cells. The hemolysis effects are profoundly proteolytic, and this venom 

offers homeopathy some interesting challenges. 

245

Venoms of the viper family are potent in their ability to digest different 

cells. In fat, small tears in the blood vessels can occur as a result of this 

venom. The action of the proteolytic enzyme in the venom can also 

produce necrosis. The venoms of the rattlesnake viper family can have 

strong necrotizing effects. Oftentimes necrosis is seen at the site of the 

bite in the human victims who survive these snake bites. The proteolytic 

effects kill cells homeopathically. It can restore life to necrotized areas, as 

in peripheral circulatory disease. 

Edema and swelling occur after many different snake bites because 

they start histamine cascades. A chart on some of the hemorrhagic and 

proteolytic effects of snake venom is shown below. 

246

Key: 

Distribution of Hemorrhagic, Lethal and Proteolytic Activities 

in Snake Venoms 

Snake Venom 

A: Agkistrodon 

C: Crotalus 

T: Trimeresurus 

(Ohsaka, A. et al., 1960) 

Hemorrhagic 

activity 

MHD(μg) 

247 

Lethal 

activity 

LD50(μg) 

Proteolytic 

activity 

(units/mg) 

LD50 

/ 

MHD 

A. contortrix 

contortrix 

1.90 200 33.7 105 

A. contortrix mokasen 1.20 125 48.1 104 

A. piscivorus 

piscivorus 

0.80 60.0 41.5 75 

A. halys 0.14 16.0 35.8 114 

Bothrops atrox 2.11 5.6 44.5 2.7 

Bothrops jararaca 0.75 18.5 74.0 25 

C. adamanteus 0.04 18.5 9.76 462 

C. atrox 0.43 45.0 83.6 105 

C. durissus terrificus 18.0 3.6 39.2 0.2 

C. viridis viridis 0.56 21.0 39.5 38 

T. flavoviridis 0.20 54.0 33.0 270 

T. flavoviridis 

tokarensis 

1.15 160 37.8 139 

T. elegans 0.30 71.0 13.0 237 

T. okinavensis 1.38 140 69.0 102 

Vipera russellii 21.0 2.2 5.56 0.1 

Vipera ammodytes 0.47 7.4 41.7 16 

Vipera palestinae 0.54 7.1 4.96 13 

Cuasus rhombeatus 0.81 › 250 0.26 › 309 

Bitis arietans 0.15 15.0 18.7 100 

Bitis gabonica 0.04 13.5 11.7 338 

Ophiophagus hannah 0.84 54.0 12.0 64 

Bungarus fasciatus › 100 a 18.5 0.06 ‹ 0.18 

Naja melanoleuca 100 6.0 7.00 ‹ 0.06 

Naja naja atra › 100 a 8.0 0.12 ‹ 0.08 

Naja naja 100 5.6 2.85 ‹ 0.06

This type of histamine release is compounded by other toxins. Many 

rattlesnakes have strong histamine releasing proteins which help to 

complicate the involvement of their venoms. A list of the different venoms 

and their effect on histamine and serotonin content is shown below. 

Effect of Venoms from Different Species of Snakes on the Histamine 

(H) and Serotonin (S) Content of Isolated Rabbit Platelets 

(Markwardt, F. et al., 1966) 

Venom Concentration 

(μg/ml 

a 0 = no release: ++ = over 50% release: + = less than 50% release. 

248 

Effect a 

H 

Naja flava, N. haje 100 0 0 

N. naja, N. n. oxiana 

N. nigricollis 100 ++ ++ 

Bungarus fasciatus 100 0 0 

Dendroaspis viridis 100 0 0 

Bitis arietans 100 0 0 

Echis carinatus 100 0 0 

Vipera ammodytes 

V. berus, V. russellii 100 0 0 

Agkistrodon piscivorus 100 0 0 

A. contortrix 100 + 0 

Bothrops alternate 100 0 0 

B. neuwiedii 100 0 0 

B. cotiara, B. insularis 10 + 0 

B. jararacussu 10 + + 

B. jararaca 10 ++ + 

Crotalus adamanteus 

C. atrox, C. viridis 100 0 0 

Lachesis muta 

Sistrurus catenatus 100 ++ ++ 

Crotalus horridus 10 ++ ++ 

C. durissus terrificus 10 + + 

C. durissus terrificus 1 ++ ++ 

C. durissus terrificus 0.1 + + 

Effect a 

S

Another area to explore is the liberation of pharmacologically active 

substances by different snake venoms. Snake venoms can activate and 

release histamine, serotonin (five-hydroxytryptamine), and bradykinin. 

Some slow-reacting substances can be released such as prostaglandins 

and lysophosphatides, catecholamines such as adrenaline, chetosteroids, 

and finally, anaphylatoxin. Anaphylaxis can also be stimulated by certain 

venoms, or treated with dilute forms of same. 

Another dangerous fact about snake venoms is their nephrotoxicity. 

The kidney is affected in almost all types of snake bites. Venom can 

produce renal lesions including glomerulitis, glomeronephritis, arthritis, 

interstitial nephritis, tubular necrosis, cortical necrosis, and renal 

infarct. Renal failure is oftentimes the most common result, as well as 

hematuria, myoglobinuria, hemoglobinuria, and proteinuria. 

Probably the most frequently used remedy in homeopathy from snake 

venom is Lachesis. This venom comes from Lachesis trigonocephalous, a 

large South American snake from three to fourteen feet long. Its 

poisonous venom was first used by Dr. Constantine Hering of 

Philadelphia. The Lachesis is prepared at 6x and higher; proportions 

below 6x may be dangerously toxic. 

In its raw form this can produce a poisonous condition of the blood 

which causes hypersensitivity in the body. The patient usually reports 

that he cannot bear anything tight around the throat. This is known as a 

left-sided remedy, as it usually affects the left side in its raw form. There 

is a general aggravation of conditions after sleep which indicates 

Lachesis must be used. Blueness of the skin and eruptions can appear. 

Some of the other homeopathic indications are loquacity where the 

patient jumps from one subject to another; jealousy, fear of being 

poisoned, and sometimes the patient imagines that he is under some 

superhuman control. Headache over the left eye accompanying a cold, 

with the headache worsening in the heat of the sun might also indicate 

that Lachesis may be needed. 

249

Facial erysipelas that first appear as red and then dark bluish or 

purplish, with more on the left side, can also indicate the need for 

Lachesis. Watery discharge from the left nostril, throbbing headache 

relieved when the discharge appears; dry tongue protruded with 

difficulty, cracked tongue at the tip which is brown on the dorsum, great 

difficulty in swallowing, high fever, exhaustion, a craving for oysters, 

horribly offensive diarrhea, ovarian trouble (often pain in the left ovary), 

menses which are scanty, feeble, black or offensive; and pain in the hips 

(bearing down on the left ovary, better when flow is established) are some 

of the conditions which can indicate that Lachesis is needed. 

Crotalus, the rattlesnake venom, is a classic homeopathic which Dr. 

Hering also wrote about. Its homeopathic indications are often a 

yellowness of the skin from disintegration of the blood and a tendency to 

hemorrhage. In yellow fever, crotalus is often indicated in the stage of 

black vomit when there is low delirium, yellow skin, and oozing of blood 

from every orifice. 

Naja is aother classic homeopathic venom found in the cobra Naja 

tripudians. It is often used in degenerative diseases as well as in valvular 

diseases of the heart, with a dry, teasing cough present. 

Another is the elaps, a type of Elaps corallinus. This is the coral snake 

venom which was first introduced homeopathically by Dr. Benoît Jules 

Mure of Brazil. Some initial homeopathic indications for elaps are: 

sniffles in children, stuffed up nose, and a great sense of coldness in the 

stomach from cold water. 

Another type of venom used in classical homeopathy is the Bufo rana, 

or the South American toad. Many South American toads have sweat 

that contains neurotoxins. These are noted to affect the sexual system, 

and Bufo rana has been used widely for sexual deviance and for many 

other types of cases as well. Bufo rana has been used to help encourage 

sexuality and to treat cases of frigidity. Its usual dose in those cases is 

100x or above. 

250

The Colorado River toad venom is known to cause epilepsy, as many of 

the different toad venoms do. Homeopathic treatment of epileptic 

conditions consists of different toad venoms. 

Sepia succus is an inky secretion released by the cuddle fish when it is 

pursued by its enemies. The cuddle fish releases it as a “dummy target,” 

allowing the cuddle fish to go unnoticed. This Sepia product has been 

widely used in homeopathy for many kinds of conditions. The five general 

characteristics of sepia are: 1) weakness, 2) yellow complexion, 3) 

bearing-down sensation, 4) violent motion that relieves the symptoms 5) 

the amelioration of symptoms at midday. The mental symptoms of sepia 

include weak memory, helplessness, susceptibility to excitement, 

susceptibility to terror, despair, fear of being alone (the person wants 

company desperately), and headaches (more common in the morning), 

increasing as the day goes by, relieved by sleep or violent motion. The 

patient who is sad and tearful with headache feels better in open air. 

Menstrual headache can also be noted. 

Blue Octopus venom produces blood disorders similar to leukemia. It is 

powerful homeopathically in the treatment of leukemia 

Many spider venoms are of value for homeopathic use. The tarantula 

venom, known as Tarantula hispaña, helps in cases of restlessness. The 

patient needing this will always be in constant motion, even though 

motion aggravates most of the symptoms. The person must be doing 

something all the time. This venom becomes very useful with patients 

who are hysterical. 

Tarantula cubensis relieves the atrocious pain that accompanies a 

sloughing carbuncle. 

Black Spider venom, also known as Mygale lasiodora, is used in chorea 

where there is twitching of the facial muscles, irregular convulsive 

movements of one side of the body, words are jerked out, and the 

movements cease during sleep but return more violently in the morning. 

251

Theridion, spider venom from Theridion curassavicum or the orange 

spider is found in the West Indies. This venom can produce throbbing 

pains over the left eye which is aggravated in the heat of the sun. Noise 

aggravates it as well. This pain is associated with vertigo, and often 

times, nausea. It is worsened by closing the eyes, motion or jarring, or 

walking across the floor. There is extreme sensitivity to noise. This 

venom is very good for conditions of cardiac anxiety. 

The cross spider, known as Aranea diadema, is a large black spider of 

the central United States. Two particular symptoms directing one to 

aranea are numbness of the parts of the body supplied by the ulnar 

nerve, and boring, digging pain in the oscalcis. 

Black widow venom gives dramatic help for many neurological 

conditions, especially peripheral neuropathy. 

Scorpion venoms are powerful in homeopathy. They usually cause 

paralysis, pains and weakness, and can be used to reverse some of those 

same conditions. 

Even the venom from the ant can have homeopathic effects. Ant venom 

is very rich in formic acid, and this causes inflammation and irritation; 

thus, ant venom can help reverse such conditions. 

The venom of the honey bee, Apis mellifica, is highly important in 

homeopathy as it produces certain types of conditions. The characteristic 

symptoms of Apis are: 1) drowsiness, 2) edema, 3) thirst, 4) intolerance of 

heat, 5) stinging pains, 6) aggravation in the afternoon (between 4:00 and 

6:00) and 7) bruised sensations. Meningitis can often be treated with 

Apis. Oftentimes the patient is fidgety, awkward, clumsy, and silly; 

laughs, drops things, and is often very jealous. 

Wasp venom can have very powerful implications in homeopathy, as 

can the Spanish fly or cantharis. 

With this brief review of venoms that nature offers, some intriguing 

protein compounds can be utilized. Many of these venoms follow the 

Arndt-Schultz principle and have reverse action in small, dilute 

252

homeopathic forms, whereas many of these venoms can be utilized in low 

doses to accomplish other tasks. There are hundreds of thousands of 

insects, spiders, snakes, and animals that carry different venoms. These 

venoms have had dramatic potential in shaping medicine. They offer 

medicine profound techniques in treating the myriad of diseases found in 

the human being. 

This is another reason why it is such a tragedy to destroy our rain 

forests. Many of the people going to the rain forests are looking just for 

plants, herbs, and fungi that might be used in pharmaceuticals, not 

realizing that some of the most potent pharmacological acting agents in 

the rain forests come from the venoms of these different insects and 

animals which are becoming extinct. We must stop cutting down the rain 

forests and look in as many different places as we can to find ways to let 

nature heal. Nature can heal, and man can destroy. 

This short treatise has been only a brief introduction to some of the 

pharmacological ways that venoms can be used in homeopathy. 

253

Summary of Immunopathology, Histopathology, and Electron-microscopic findings of the Kidney in Snakebite 

Histopathology Electron-microscopy 

Immunopathology 

Location of deposits 

Arteriolar Arterial Proliferation Tubular Necrotizing Thrombophlebitis Glomerular Glomerular Tubular 

wall wall of glomerular necrosis and arteritis 

electron- basement degeneration, 

mesangial regeneration 

dense membrane necrosis and 

cells 

deposits alteration regeneration 

C3(=) C3(+) + ++ + + + - + 

Glomerular 

capillary 

Type of 

Snake 

1gM 

(+ to ++) 

Russell’s 

viper 

C3(=) 

+ to ++ + - + + b - + 

C3(=) No 

deposit 

1gM (trace to 

+) 

C3(=) 

Green 

pit viper 

Fibrin a 

+ - - - + + - 

C3 (=) No 

deposit 

1gM (+) 

C3 

Cobra 

(+ to ++) 

- = Negative 

+ = Mild 

++ = Moderate 

a 

= Focal deposition 

b 

= With deposition of fibrin 

255

Renal Failure with Known Lesions in Various Snakebites 

Snake Renal Lesion 

Crotalus terrificus Tubular necrosis 

Cryptophis nigrescens Tubular necrosis 

Sea snake Tubular necrosis 

Russell’s viper Tubular necrosis 

Echis carinatus Cortical necrosis 

Borthrops jararaca Cortical necrosis 

Agkistrodon hypnale Cortical necrosis 

Bitis arietans Proliferative 

glomerulonephritis 

Cases with renal failure without known snake or renal 

lesions are not included. 

255

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poisoning in man; histopathologic study. Am J Pathol 1954; 30 (3):479- 

99. 

Angeletti RA. Studies on the nerve growth factor (NGF) from snake 

venom. Gel filtration patterns of crude venoms. J Chromatogr 1968a; 36 

(4):535-7. 

Angeletti RH. Nerve growth factor (NGF) from snake venom and mouse 

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(1):234-7. 

Angeletti RH. Nerve growth factor from cobra venom. Proc Natl Acad Sci 

U S A 1970a; 65 (3):668-74. 

Angeletti RH. The role of the tryptophan residues in the activity of the 

nerve growth factor. Biochim Biophys Acta 1970b; 214 (3):478-82. 

Angeletti RH. Studies on the nerve growth factor (NGF) from snake 

venom molecular heterogeneity. J Chromatogr 1968b; 37 (1):62-9. 

Arthus M. Venomous poison and proteinic poison. Comptes Rendus 

Hebdomadaires Des Seances De L’Academie Des Sciences 1912; 154:79. 

Arthus M. The specificity of anti-venomous serums. Anti-cobra, antibothropic 

and anti-whip snake serums. Venoms of the Lachesis 

lanceolatus, the Crotalus terrificus and the Crotalus adamanteus. 

Comptes Rendus Hebdomadaires Des Seances De L’Academie Des 

Sciences 1911; 153:1504-1507. 

Arthus M. Regarding poisoning by snake venom. Comptes Rendus 

Hebdomadaires Des Seances De L’Academie Des Sciences 1911; 153: 

482-484. 

Azevedo AP, Teixeira JC. Intoxicacao per veneno de cobra, necrose 

symetrica da cortex renal. (Cobra snakebite intoxication, necrosis of the 

renal cortex) Mem Inst Oswaldo Cruz 1938; 13:23-38. 

Bailey GS, Banks BE, Pearce FL et al. A comparative study of nerve 

growth factors from snake venoms. Comp Biochem Physiol B 1975; 51 

(4):429-38. 

Banks BE, Banthorpe DV, Berry AR et al. The preparation of nerve 

growth factors from snake venom. Biochem J 1968; 108 (1):157-8. 

256

Chugh KS, Pal Y, Chakravarty RN et al. Acute renal failure following 

poisonous snakebite. Am J Kidney Dis 1984; 4 (1):30-8. 

Chugh KS, Aikat BK, Sharma BK, Dash SC, Mathew MT, Das KC. Acute 

renal failure following snakebite. Am J Trop Med Hyg 1975 Jul ; 

24(4):692-7. 

Cohen S. Purification and metabolic effects of a nerve growth-promoting 

protein from snake venom. J Biol Chem 1959; 234 (5):1129-37. 

Cohen S, Levi-Montalcini R. A Nerve Growth-Stimulating Factor Isolated 

from Snake Venom. Proc Natl Acad Sci U S A 1956; 42 (9):571-4. 

Cunningham, DD. The physiological action of snake-venom. In: 

Scientific Memoirs by Medical Officers of the Army of India, Part IX. 

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India. 

Furtado MA, Lester IA. Myoglobinuria following snakebite. Med J Aust 

1968; 1 (16):674-6. 

Hering C. Hering’s Action of the Snake Poisons. British Journal of 

Homeopathy. Vol. 11 & 12. 

Hogue-Angeletti RA, Frazier WA, Jacobs JW et al. Purification, 

characterization, and partial amino acid sequence of nerve growth factor 

from cobra venom. Biochemistry 1976; 15 (1):26-34. 

Markwardt F, Barthel W, Glusa E. [Changes in the serotonin and 

histamine content of blood platelets due to the effect of local anesthetics]. 

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44. 

Marsden AT, Reid HA. Pathology of sea-snake poisoning. Br Med J 1961; 

1 (5235):1290-3. 

May RM, Guimard J. [Stimulating action of venoms from the snakes 

Vipera, Naja, Bitis and Echis on the growth of chick embryo spinal cord 

fibers in vitro.]. C R Hebd Seances Acad Sci 1959; 248 (18):2657-9. 

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Mohamed AH, Saleh AM, Ahmed F. Nerve growth factor from Egyptian 

snake venoms. Toxicon 1971; 9 (3):201-4. 

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Serpents Ann Inst Pasteur. 1904; 18:387-406. 

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snake venom, and their relations to lethal toxicity, proteolytic activities 

and other pathological activities. Br J Exp Pathol 1960; 41:478-86. 

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Br Med J 1963; 1 (5346):1647-8. 

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characterization of nerve-growth factor from the venom of Vipera russelli. 

Eur J Biochem 1972; 29 (3):417-25. 

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adamenteus snake venom. J Biol Chem 1978; 253 (17):6140-8. 

Rogers L. The physiological action and antidotes of snake venom with a 

practical method of treatment of snake bites. Lancet 1904; 1:349-355. 

Seedat YK, Reddy J, Edington DA. Acute renal failure due to proliferative 

nephritis from snake bite poisoning. Nephron 1974; 13 (6):455-63. 

Server AC, Herrup K, Shooter EM et al. Comparison of the nerve growth 

factor proteins from cobra venom (Naja naja) and mouse submaxillary 

gland. Biochemistry 1976; 15 (1):35-9. 

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venom. J Physiol. London 1887; 8:203-10. 

Sitprija V, Benyajati C, Boonpucknavig V. Further observations of renal 

insufficiency in snakebite. Nephron 1974; 13 (5):396-403. 

Sitprija V, Sribhibhadh R, Benyajati C. Haemodialysis in poisoning by 

sea-snake venom. Br Med J 1971; 3 (5768):218-9. 

Stephens JW, Meyers W. Test-tube reactions between cobra poison and 

its antitoxin. Lancet. March 5, 1898; 1:644-46. 

Varagunam T, Panabokke RG. Bilateral cortical necrosis of the kidneys 

following snakebite. Postgrad Med J 1970; 46 (537):449-51. 

258

GEMMOTHERAPY 

Gemmotherapy consists of making herbal remedies from the buds or 

shoots of young plants. These remedies cleanse cells of toxins through 

digestion, urinary tract, lung, and skin. Some of the remedies can be 

found below. 

Abies Pectinata: Decalcification and rickets, dental caries 

Acer Campestres: Sequelly of poliomyelitis and paralysis, Herpes Zoster 

Aesculus Hippocastanum: Hemorrhoids 

Alnus Glutinosa: Sequelly of cerebral hemorrhage, cerebral infarction, 

chronic rhinitis 

Alnus Incana: Arthritis 

Ampelopsis Weitchii: Chronic rheumatism, rheumatoid arthritis 

Betula Pubescens: Intellectual overwork, psych-asthenia 

Carpinus Betulus: Spasmodic and chronic rhino-pharyngitis, spasmodic 

cough 

Castanea Vesca: Venous congestion 

Cedrus Libani: Dry eczema, ichthyosis, pruritus 

Cercis Siliquastrum: Improves arterial circulation 

Citrus Limonum: In the presence of an increase in blood fibrinogen 

levels 

Cornus Sanguinea: Enhanced coagulation 

Corylus Avellana: Emphysema and pulmonary fibrosis 

Crataegus Oxyacantha: Cardiac insufficiency, precordial pain, 

tachycardia, sequelly of infarction 

Fagus Sylavaatica: Renal insufficiency, renal lithiasis 

Ficus Carica: Obsessional and anxiety neurosis, gastric and peptic 

ulcers 

Fraxinum Excelsior: Acute and chronic gout 

Ilex Aquifolium: Gout or urethema 

259

GEMMOTHERAPY, cont. 

Juglans Regia: Varicose ulcers, skin infections (impetigo, infected 

eczema) 

Juniperus Communis: Major hepatic insufficiency and cirrhotic 

syndromes 

Olea Europaea: Hypertension, arteriosclerosis, hypercholesterolemia 

Pinus Montana: Chronic rheumatism, vertebral osteoarthrosis, 

osteroarthrosis of the hips and knees 

Platanus Orientalis: Urticaria with accompanying inflammation, itching, 

and discomfort 

Pulus Nigra: Obliterative arterial disease of the lower limbs and 

associated trophic disturbances 

Prunus Amygdalus: Vascular sclerosis, hypertension 

Quercus Pedonculata: Increases the bodily defense mechanisms 

Ribes Nigrum: Allergic problems, chronic coryza, hay fever, migraine 

Rosa Canina: Migraine and headache 

Rosmarinus Officinalis: Hepatic insufficiency, biliary colic, biliary 

dyskinesia 

Rubus Fructicosus: Female problems, menstrual disturbances, pelvic 

pain, metritis and vaginitis 

Secale Cereale: Hepatic insufficiency 

Sequoia Gigantea: Prostatic hypertrophy and adenoma, uterine fibroids 

Sorbus Domestica: Venous problems, sequelly of phlebitis, haemogliasis 

Syringa Vulgaris: Arterial sclerosis or improved arterial circulation 

Tamaris Gallica: Various types of hypercholesterolemia 

Tilia Tomentosa: Nerve sedative, tranquilizer, insomnia, neuralgia 

Ulmus Campestris: Weeping eczema, acne and impetigo 

260

GEMMOTHERAPY, cont. 

Vaccinium Vitis: Intestinal syndromes, chronic E. coli infections 

Viburnum Lantana: Simple and complicated asthma 

Vitus Vinifera: Bone metabolism and inhibits proliferative deformities 

such as osteophytes 

Zea Mais: Favors post infarction healing of cardiac tissue and produces a 

fall in blood transaminase levels 

Source: http://homeoinfo.com/08_nonclassical_topics/is_it_homeopathy/gemmotherapy.php 

261

Acetonum 

Acetyl Choline Chloride 

Acid Cic-Aconite 

Acid Citricum 

Acid Fumaricum 

Acid Glutaminicum 

Acid Malic 

Acid Pyruvicum 

Acid Succinicum 

Adipinic Acid 

Allergy Malus 

Aloe 

Alpha-Ketoglutaaric Acid 

Alumina 

Ammonium Carb. 

Ammonium Phos. 

Anacardium 

Apis Mel. 

Arnica 

Arsenicum Alb. 

Bar. Oxalsusccinicum 

Belladonna 

Bentonite 

Benzinum Crudum 

Benzpyrene 

Berberis 

Bilirubinum 

Bryonia 

Bufo Rana 

Butter Yellow 

Calendula 

Cantharis 

Caprolactam 

Caprylic Acid 

Capsicum 

Carbo An. 

Carbo Veg. 

Carboneum Tetrachloratum 

Cardus Mar. 

Carrageenan (Type 1, 

Lycopodium) 

Carrageenan (Type 5, 

Lycopodium) 

CLASSICAL HAHNEMANIAN SINGULARS 

262 

Cactus Grande 

Caulophyllum 

Cell Salts (All) 

Chamomilla 

Cehlidonium 

Chlorcamphor Menthol 

Chlormphenicol 

Chloroformium 

Chlortetracycline 

Cholesterinum 

Chromium Oxide 

Cina 

Cinchona 

Congo Red 

Cortisone 

Crataegus 

Cysteinum 

Cystinum 

Digitalis 

Dimethyl terephthalate 

Diphenylamine 

Diphenylhydantoin 

Di-Sodium Phosphate 

DNA 

Echinacea 

Estradiolbenzoate 

Ethylene Glycol 

Ethylene Oxide 

Evening Primrose 

Formaldehyde Dehydrogenase 

Formaldehyde Sol. 

Formic Acid 

Fumaria 

Fucus Vesiculosus 

Germanium 

Glutaminum 

Glycerinum 

Glycocollum 

Glycogen 

Glyoxal 

Graphites 

Hamamelis Virginica 

Harnsaure (Acid. Uric)

Classical Hahnemanian 

Singulars, cont. 

Hepa Sulph. 

Hexamethylentetramin 

Hirudinum 

Histidinum 

Hyaluronidase 

Hydrangea 

Hypoxanthinum 

Ignatia 

Indican 

Indolum 

Insulinum 

Interferon 

Ipeca 

Iris Versicolor 

Isoniazide 

Isotonic Plasma 

Jodoformium 

Juglans 

Kali Carb. 

Kreatinum 

Lachesis 

Lithium Nitrate 

Lycopodium 

Macrodantin 

Mag Phos. 

Mercurius 

Methylethylketon 

Naja 

Natrum Muriaticum 

Natrum Sulph. 

Nux Vomica 

Oleander 

Paraffinum 

Penicillinum 

Peptonum 

263 

Petroleum 

Phenacetinum 

Phenylalanine 

Phosphorous 

Phytolacca 

Plasma (Horse) Prophlthiouracil 

Pulsatilla 

Rauwolfia 

Rhus Tox. 

Ruta Grav. 

Sepia 

Serotonin 

Silicae (Equisetum) 

SolidagoSpigelia 

Spongia 

Staphisagria 

Sulfanilamidum 

Sulfur 

Superheated Vegetable Fat 

Tetracycline 

Thioacetamid 

Thuj 

Tryptophanum 

Ubiquinone 

Urea 

Urtica 

Vaccinnum 

Viscum Album (Gr. on Abies 

Alba) 

Viscum Album (Gr. on Acer 

Camp.) 

Viscum Album (Gr. on Populus) 

Viscum Album (All) 

Vitamin D

A NEW PERSPECTIVE ON RESEARCH 

In 1991, U.S. News and World Report published a series of articles 

about alternatives to medical techniques, and how they are getting more 

and more attention by doctors throughout America. More doctors were 

turning to alternative techniques in light of the inability to get lasting 

results via synthetic allopathy and surgical intervention. As the populace 

starts to look for more natural techniques with fewer side effects, 

alternative medicine practitioners have been developing natural types of 

therapies, and improving their skills with these natural modalities. This 

underground medical group has developed some wonderful techniques to 

deal with a wide variety of medical problems. 

It is important to note that every field of endeavor in society will have 

evolution in its thought and philosophies. There can be no eternal 

stagnation in the philosophy or psychology of any group. 

Through the years medical philosophy has created many different 

foundations which have yielded over time. Medicine started with very 

natural philosophies and became more statistical and analytical after the 

development of statistics by Poincare. Synthetic chemistry came along 

and offered its processes, and the dramatic amount of profitability which 

could be incurred from patenting such items further helped to develop 

the synthetic cause, thus leading to an allopathic philosophy primarily 

based on synthetic chemistry and surgical intervention. This is the basic 

mind set which has developed in medicine over the last fifty years and 

which is now starting to yield to other fields of endeavor. Some of them 

are electronics, physics, energetics, naturopathy, and homeopathy. 

There is a new psychology of medicine which will develop over the next 

five to ten years, and will have a softer philosophy, making up for some 

of the mistakes made in the past due to synthetic allopathy. 

As we observe this process of the psychological evolution in medical 

philosophy, it is important to note that it parallels the psychological 

264

evolution of the minds of men. This chapter is dedicated to a new 

concept of medical psychology and philosophy. The opponents of this 

development will try to cling to old style ideations, and they will also 

secure themselves in the arrogant, obstinate stance of being judgmental. 

This attitude might stop them from reading and getting the benefits that 

this treatise has to offer. We hope that they can soften their hearts and 

minds to allow a new psychology and philosophy to develop freely. 

In this U.S. News and World Report article, several different modalities 

were addressed: acupuncture, biofeedback, homeopathy, nutrition, 

naturopathy and others. Please see full-text article below. 

BIG CLAIMS, NO PROOF 

A look at farther-out cures, from aromas to reflexology 

Mainstream doctors may wonder why anyone with heart 

disease would take herbs instead of a beta blocker. Yet 

the claims for alternative healing are intriguing, if 

largely unproven. Here's a guide to six treatments. 

HOMEOPATHY 

WHAT IT IS. A medical system based on the teachings 

of Samuel Hahnemann, a German doctor who in the 

1800s believed that symptoms such as fevers should 

not be suppressed because they represent the body's 

efforts to repel disease. 

THE CLAIM. Diseases can be cured only by using drugs 

that echo the symptoms. A feverish person, for example, 

would be given a drug that would raise body 

temperature. And the drugs should be administered in 

doses so diluted they are practically undetectable. 

THE EVIDENCE. An analysis of 105 controlled though 

sometimes poorly executed studies published worldwide 

found ''positive'' results for homeopathy treatments in 

81 trials, according to a report in last February's British 

Medical Journal. The results provide a basis for 

continued research, the authors conclude -- with betterdone 

trials. 

265

HERBALISM 

WHAT IT IS. An ancient system of medicine in which 

preparations of leaves, stems, seeds and roots are 

consumed or rubbed on the body. 

THE CLAIM. Herbal remedies contain natural 

ingredients as potent as synthetic drugs but often safer. 

THE EVIDENCE. Plant extracts can indeed be valuable; 

researchers constantly seek out new possibilities. May's 

Proceedings of the Society for Experimental Biology and 

Medicine, for example, reports that Andrographis 

paniculata, an herb used in China to cure hepatitis, 

dysentery and meningitis, also hampers reproduction in 

lab tests of the human immunodeficiency virus, which 

causes AIDS. But a report in Allergy last year found that 

herbal treatments for rashes made symptoms worse. 

NATUROPATHY 

WHAT IT IS. A therapy dating to 19th-century Germany 

that relies on air, sunshine, water, heat, massage and 

herbs to cure both the body and the mind. 

THE CLAIM. Illnesses from colds to typhoid can be 

cured by purging the body of poisons, accomplished 

through fasting, salt-water baths, breathing and 

relaxation exercises -- even psychotherapy. 

THE EVIDENCE. Few controlled trials have produced 

conclusive results. 

AROMATHERAPY 

WHAT IT IS. An ancient Chinese form of herbal 

medicine that seeks to cure illnesses with the aromatic 

oils of plants. 

THE CLAIM. Plant essences are massaged into the skin, 

used as bath oils, inhaled and, in very rare cases, even 

ingested. 

THE EVIDENCE. Scents can indeed evoke strong 

emotions. Recent studies also show that certain scents, 

like peppermint, can increase workers' productivity and 

266

Reference 

vanilla's aroma can be relaxing. But whether scents can 

cure diseases like gastrointestinal disorders, as is 

claimed, is as yet unproven. 

MAHARISHI AYUR-VEDA 

WHAT IT IS. A form of natural healing based on ancient 

Indian texts recently translated for Westerners by 

Maharishi Mahesh Yogi, who introduced the world to 

transcendental meditation. 

THE CLAIM. All illness results from ''imbalances'' in 

such functions as respiration, circulation and 

metabolism and can be treated through meditation, 

massage and herbal medicines. 

THE EVIDENCE. In May, the Journal of the American 

Medical Association ran a three-page letter -- not a 

study -- from proponents citing positive findings from a 

range of investigations. One U.S. study found that socalled 

Ayurvedic herbal compounds reduced the 

incidence of breast cancers in ''up to 88 percent'' of 

experimental animals. It will take many solid studies to 

make doctors overlook Ayur-Veda's mystical precepts. 

REFLEXOLOGY 

WHAT IT IS. A massage technique that attempts to 

treat diseases and keep the ''life force'' in balance. Its 

origins can be traced to ancient China. 

THE CLAIM. Areas on the soles and sides of the feet 

govern ''energy channels'' that extend throughout the 

body. By massaging specific spots on the foot, a 

reflexologist can sense and unblock clogged channels. 

THE EVIDENCE. No controlled clinical trials are 

described in medical journals. 

Podolsky, Doug. U.S. News & World Report. Big Claims, No 

Proof. 23 September 1991. Vol. 111, Issue 13, p77. 

267

The critique of homeopathy was that there were not enough apparent 

clinical trials. It is the purpose of this article to question the very 

foundation of clinical trials as the end all deciding factor in whether 

procedure or medical belief is acceptable or worthwhile in medicine. 

The factor of clinical trials means that once an item or drug is chosen it 

can be put to a clinical test in the patient population to see if it really 

does that for which it was originally designed. 

To do a clinical trial, a randomly selected group of patients, possessing 

whatever traits we would be looking for (such as diabetes, high blood 

pressure, or any other type of medical illness) would be selected. Then, a 

controlled population or group is selected. We now give the substance, 

the therapy, to a certain number, known as the “effect group”, and the 

control group would get a placebo, or some other type of comparative 

therapy regime. We now do a statistical manipulation at the end of this 

study, whatever time line it might be, to see if the purported remedy 

would work better than placebo in the study. Comparative statistics 

would be used to evaluate whether the substance performed well versus 

the placebo or control group. This is an over-simplification of a statistical 

clinical trial. 

The purpose and the basis of our study is to challenge the Null 

hypothesis. The Null hypothesis: the two groups which are being 

statistically challenged will be equivalent, and will not show any 

difference. If the Null hypothesis is disproved, and the two groups are 

different, then we can assume that there is statistical evidence that one 

group outperforms the other by some criteria. 

The problem with modern medical statistical analysis is that if the two 

groups are proved equal, and the Null hypothesis is not disproved, then 

the assumption is that the two therapies are equivalent. This is not what 

the Null hypothesis states, as it was originally set up for analysis. The 

true conclusion is that the groups differed, but the difference in the two 

groups could not be detected by the limitations of our measurements. 

268

Thus, in determining that synthetic vitamins are equivalent to natural 

vitamins in the statistical studies we must clarify that the Null 

hypothesis does not state that the two groups are equivalent; just that 

the sophistication of our measurement skills is not sufficient to measure 

the difference. This is the true conclusion which can be achieved from 

the Null hypothesis. But oftentimes in science the Null hypothesis is 

abused as in assuming that two groups are equivalent, when actually 

there might be a problem with accuracy skills. 

As we have pointed out, reductionism is often a problem in science, not 

the solution. In doing these types of studies we see the errors of 

reductionism at their finest. 

269

PROBLEMS WITH CLINICAL TRIALS 

� Reductionism. Reducing the complex patient to simple 

measurements. This makes attained information suspect and 

weak. Medicine becomes cold, impersonal, and statistical. 

Compassion cannot be reflected by statistics. 

� Never long enough. Effects of a synthetic medication can result in 

genetic damage generations later. 

� Overconfidence and misinterpretation of the Null hypothesis. If a 

study of natural vs. synthetic vitamins shows no difference in 

results, it does not occur to researchers that they or their ability to 

measure could be in error. 

� Most always benefits the one who can afford to fund the study. 

Experimenter effect. 

� Trials will always reward and reinforce the philosophy of those 

performing them. Allopathy is preferred; homeopathy and 

naturopathy are ignored. 

� Quantity does not dispel quantity. Publish or perish rule pushes 

paper out of educational institutions which just perpetuates the 

allopathic delusion. 

� Inability to accept the truth that allopathy is hurting patients in 

vast numbers. Iatrogenic malpractice suits resulting from synthetic 

drugs top fifteen billion dollars a year. We must realize that our 

clinical trial process is a failure, and replace it. 

These errors of reductionism result in errors of decision-making within 

the medical establishment. As we take these individuals with rampant, 

variant problems, different conditions of liver function, kidney function, 

skin conditions, ethnic backgrounds, and the like, we then take these 

populations and reduce them to one type of criteria. We reduce the 

complexity of their human diversity to a simple variable of blood 

pressure, hormone level in the blood, range of motion, or whatever type 

of statistical measurement technique we use. 

270

There are possibly millions, if not millions of millions of variables which 

can be measured in the human body. The body is vastly complex. No 

known study has ever measured all of the variables possible to achieve a 

total analysis. Every known study has been reductionistic in some way. 

It is necessary to realize the inadequacy of statistical information, and 

not revere them or put them on the pedestal created by modern science. 

SOLUTIONS TO CLINICAL TRIAL PROTOCOLS 

� Realization of the inadequacy of any clinical trial to give perfect 

conclusions. Incorporate compassion, education, and love back 

into medicine. 

� Nature has designed chemicals and complex compounds such as 

herbs and glandulars for millions and millions of years. 

Naturopathy comes with its own long-term background study. 

� Realize that the Null hypothesis only says that this study showed, 

not proved, no effect. 

� Reduce restrictions on orphan drug funding and encourage more 

natural drug testing by reducing philosophical criticisms. 

� Broaden our philosophy of medicine to revere the natural process 

and acknowledge the unknown in biology. 

� Give equal funding to studies on homeopathy and naturopathy at 

educational institutions. 

� Broaden our medical philosophy to include quantum theory, 

energetics, homeopathy and naturopathy. Teach doctors that there 

is a safer and more compassionate way to do medicine. “First don’t 

hurt” must be brought back into medicine. Clinical trials should 

only be a small part of medical consideration, and not deified. 

As has been stated several times, the concept of reductionism is the 

fallacy, the error of science. Not that reductionism is totally bad; it must 

be a part of our decision-making process. But to make it the only part, 

the pinnacle, the demigod of medicine, is where the error lies. Using 

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eductionistic studies to shape medical protocol has resulted in a 

medical establishment which is about to collapse under the weight of 

iatrogenic diseases and malpractice payments. 

In science, the Null hypothesis is often talked about, meaning that we 

try to prove an experiment with the Null hypothesis. As an example, our 

hypothesis might be that digitalis can help heart patients. The Null 

hypothesis is that digitalis does nothing, and actually is no different from 

a placebo. To test our Null hypothesis we work up a random-sample 

group, wherein two populations will receive different treatments. One will 

get digitalis and one will get a placebo. If both groups experience equal 

results, then the Null hypothesis is proven; there is no difference 

between the groups or the interventions. This basic assumption is 

incorrect in the true management of science. In the true management of 

experimental science and statistical management we will find that all 

that we know from this study is that the study could not prove any 

difference between these two materials. It is wrong to assume that the 

two materials are the same just because this study did not prove them to 

be different. 

In 1982, the Journal of the American Medical Association published an 

article about hyperactive children. (Consensus Conf: Defined diets and 

childhood hyperactivity. JAMA 1982; 248(3)290-292.) One group was 

given lemonade made with a processed white sugar and the other was 

given lemonade made with saccharin. It was found that there was no 

basic difference between the two groups, and that the Null hypothesis 

was achieved. Many of the medical doctors who reported on this study 

and who were quoted on Lifetime Medical Network said that from this 

study they could conclude that there were no problems regarding 

hyperactivity generated by sugar. That was an irregular conclusion. The 

actual conclusion is that there is no difference between saccharin and 

processed sugar, but the study did not involve any natural sugars or 

fruit sweeteners. 

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Just because the study tells us that there are no differences does not 

mean that differences do not exist. One such example of bad science has 

happened over the last fifty years: during this time scientists have found 

from their studies that there is no difference between natural and 

synthetic compounds. 

Thus, a natural vitamin was found to have the same effect as a 

synthetic in that the two did not prove different in studies performed. 

These studies were reductionistic and flawed. Just because their studies 

could not find any difference does not mean that there were no 

differences. 

The basic misuse of the Null hypothesis has generated a tremendous 

income for synthetic pharmaceutical companies who develop synthetic 

compounds by the train-car load. Studies that do show differences 

between the natural and synthetic compounds are quickly discounted by 

the chemical companies. This brings us to a political ideation of who can 

make a true judgment on the correctness of a study, and oftentimes the 

philosophy of the judge will affect his decision. 

In America, it is complicated by the issue of freedom of choice. If a 

person truly wishes to have natural entities, and only natural entities 

put into his/her body, this is his/her choice. These natural compounds 

are dispensed under the same guidance of the Food and Drug 

Administration to guarantee safety and efficacy. Yet, synthetic chemical 

companies wish to inhibit the choice of the population and force on it 

synthetic compounds. 

Many drugs get through clinical trials and later are found to cause 

sickness in the patient population. Every year, ten to twenty 

medications, on the average, are taken off the shelves of pharmacists 

because the clinical trials were not thorough enough in finding out some 

of the different problems. Prozac was released into the medical system, 

and now much evidence is pointing to the fact that people taking Prozac 

273

might develop unstable thinking. Prozac might possibly even contribute 

to provoking a user to kill other people in fits of anger. 

Thalidomide was made available after clinical trials proved its success 

in handling morning sickness. But thalidomide produced babies born 

with flipper like appendages, and other gross genetic defects. One of my 

professors remarked at that time that it was a “blessing” that 

thalidomide caused these deformed flippers and great aberrant 

dysfunctions of genetic material. I inquired what he meant by “blessing.” 

He said that the blessing was that it was a violent enough reaction that it 

got taken off the market quickly. What if the effect of thalidomide was 

that it just lowered one’s I.Q. five or ten points? We might not have 

discovered that until several generations later. Thalidomide was taken off 

the market, altered, and released back on the market as Benedictine. 

Benedictine had just that effect, it lowered the IQ ten points, and was 

later taken off the market in the late 1980s because of its ability to alter 

genetic functioning and cause a wide variety of learning disabilities and 

other disturbances. 

The thalidomide problems were horrible, but were not pervasive 

throughout the population. The Benedictine problems were much less 

horrible, but were much more pervasive, as it affected literally millions of 

children in America. 

The following is a list of drugs that were taken off the market after it 

was found that their original clinical trials were not thorough enough to 

indicate some of the problems with them. Perhaps this list will convince 

the reader that clinical trials are not sufficient to protect the public. 

274

Acetazolamide 

Acetyldigitoxin 

Alkavervir 

Allopurinol 

Alseroxylon 

Aminophylline 

Aminosalicylate Sodium 

Amitriptyline Hydrochloride 

Amodiaquine Hydrochloride 

Ampicillin/Ampicillin Trihydrate 

Anileridine Hydrochloride 

Anisotropine Methylbromide 

Atropine Sulfate 

Azathioprine 

Bacampicillin Hydrochloride 

Bendroflumethiazide 

Benzthiazide 

Benztropine Mesylate 

Betazole Hydrochloride 

Bethanechol Chloride 

Bretylium Tosylate 

Bromodiphenhydramine Hydrochloride 

Brompheniramine Maleate 

Butabarbital Sodium 

Calcium; Meglumine; Metrizoic Acid 

Calcium Metrizoate 

Captopril 

Carphenazine Maleate 

Carprofen 

Cefadroxil 

Cephalexin 

Cephradine 

Ceruletide Diethylamine 

Chlophedianol Hydrochloride 

Chloramphenicol 

Chloramphenicol; Polymyxin B Sulfate 

Chloramphenicol; Prednisolone 

Chlordiazepoxide Hydrochloride 

Chlorhexidine Bluconate 

Chlormerodrin, HG-197 

Chloroquine Phosphate 

Chloroquine Phosphate; Primaquine phosphate 

Chlorothiazide 

Chlorpheniramine Maleate 

Chlorphentermine Hydrochloride 

Chlorpromazine Hydrochloride 

275

Chlorpropamide 

Chlorthalidone 

Chlorzoxazone 

Chymopapain 

Cisplatin 

Clindamycin Hydrochloride 

Clorazepate Dipotassium 

Codeine Phosphate; *Multiple* 

Colchicine; probenecid 

Cortisone Acetate 

Cryptenamine Acetates 

Cryptenamine Tannates 

Cyclobenzaprine Hydrochloride 

Cyclothiazide 

Cycrimine Hydrochloride 

Cyproheptadine Hydrochloride 

Cysteine Hydrochloride 

Decamethonium Bromide 

Demeclocycline Hydrochloride 

Deserpidine 

Desoximetasone 

Desoxycorticosterone Acetate 

Dexamethasone 

Dexamethasone Sodium Phosphate 

Dexbrompheniramine Maleate 

Dexbrompheniramine Maleate; Pseudoephedrine Sulfate 

Dextroamphetamine Sulfate 

Diatrizoate Meglumine 

Diazepam 

Diazoxide 

Dibucaines Hydrochloride 

Dicloxacillin Sodium 

Dicumarol 

Diethylpropion Hydrochloride 

Diethylstilbestrol 

Difenoxin Hydrochloride: *Multiple* 

Diflorasone Diacetate 

Digitoxin 

Digoxin 

Dihydroergotamine Mesylate; Heparin Sodium; Licocaine 

Hydrochloride 

Dimenhydrinate 

Dinoprost Tromethamine 

Diphemanil Methylsulfate 

Diphenhydramine Hydrochloride 

Disulfiram 

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Dopamine Hydrochloride 

Doxepin Hydrochloride 

Doxyclycine Hyclate 

Dromostanolone Propionate 

Dydrogesterone 

Dyphylline 

Epinephrine; Etidocaine 

Hydrochloride 

Epinephrine; Lidocaine 

Hydrochloride 

Ergocalciferol 

Ergoloid Mesylates 

Erythromycin 

Estradiol Valerate; Testosterone 

Enanthate 

Estrogens, Conjugated 

Estrogens, Esterified 

Estrone 

Ethchlorvynol 

Ethinyl Estradiol 

Ethinyl Estradiol; Norethindrone 

Ethoxzolamide 

Ethylestrenol 

Ethynodiol Diacetate; Mestranol 

Etidocaine Hydrochloride 

Ferrous Citrate, FE-59 

Fluocinolone Acetonide 

Fluorometholone 

Fluphenazine Hydrochloride 

Fluprednisolone 

Folic Acid 1 mg 

Gallium Citrate, GA-67 

Gemfibrozil 

Blutethimide 

Glycopyrrolate 

Gonadorelin Hydrochloride 

Gonadotropin Chorionic 

Guanabenz Acetate 

Halcinonide 

Haloperidol 

Heparin Sodium 

Hetacillin 

Hetacillin Potassium 

Hexachlorophene 

Hexocyclium Methysulfate 

Hexylcaine Hydrochloride 

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Homatropine Methylbromide 

Hydralazine Hydrochloride 

Hydrochlorothiazide 

Hydrochlorothiazide; 

Labetalol Hydrochloride 

Hydrochlorothiazide; Methyldopa 

Hydrochlorothiazide; Pindolol 

Hydrochlorothiazide; Reserpine 

Hydrochlorothiazide; Spironolactone 

Hydrochlorothiazide; Triamterene 

Hydrocodone Bitartrate; *Multiple* 

Hydroflumethiazide 

Hydroxocobalamin 

Hydroxystilbamidine Isethionate 

Hydroxyzine Hydrochloride 

Hydroxyzine Pamoate 

Ifosfamide 

Imipramine Hydrochloride 

Indocyanine Green 

Indomethacin 

Insulin Suspisophane 

Purified Pork 

Insulin Susp Protamine Zinc 

Purified Pork 

Insulin Zinc Susp, Extended 

Biosynthetic Human 

Iodipamide Sodium 

Iodoxamate Meglumine 

Isoetharine Hydrochloride 

Isoniazid 

Isoproterenol Hydrochloride 

Isoproterenol Sulfate 

Isosorbide Dinitrate 

Lactulose 

Levallorphan Tartrate 

Levodopa 

Levopropoxyphene Napsylate, Anhydrous 

Lidocaine Hydrochloride; Oxytetracycline 

Liothyronine Sodium 

Liotrix (T4; T3) 

Lithium Carbonate 

Loperamide Hydrochloride 

Loxapine Succinate 

Mannitol 

Mazindol 

Mebutamate 

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Meclizine Hydrochloride 

Meclofenamate Sodium 

Mefenamic Acid 

Mefloquine Hydrochloride 

Menadiol Sodium Diphosphate 

Menadione 

Mepenzolate Bromide 

Meperidine Hydrochloride 

Meprednisone 

Meprobamate 

Mestranol; Norethindrone 

Mestranol; Norethynodrel 

Metharbital 

Methicillin Sodium 

Methixene Hydrochloride 

Methocarbamol 

Methotrexate Sodium 

Methoxsalen 

Methyclothiazide 

Methylprednisolone 

Methylprednisolone; Neomycin Sulfate 

Methyltestosterone 

Methyprylon 

Metoclopramide Hydrochloride 

Metrizamide 

Minocycline Hydrochloride 

Minoxidil 

Molindone Hydrochloride 

Naloxone hydrochloride 

Netilmicin Sulfate 

Niacin 500 mg. 

Nitrofurantoin 

Nitrofurantoin Sodium 

Nystatin 500,000 IU. 

Orphenadrine Citrate 

Oxandrolone 

Oxazepam 

Oxybutynin Chloride 

Oxyphenbutazone 

Oxyphenonium Bromide 

Oxytetracycline Hydrochloride 

Oxytocin 

Paramethadione 

Pargyline Hydrochloride 

Paramomycin Sulfate 

Penbutololl Sulfate 

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Penicillin G Benzathine 

Penicillin G Potassium 

Penicillin G Procaine 

Penicillin G Sodium 

Penicillin V Potassium 

Pentazocine hydrochloride 

Pentobarbital Sodium 

Pentolinium Tartrate 

Perphenazine 

Phendimetrazine Tartrate 

Phenindoine 

Phenmetrazine Hydrochloride 

Phenprocoumon 

Phentermine Hydrochloride 

Phentermine Resin Complex 

Phenyl Aminosalicylate 

Phenylpropanolamine Hydrochloride; *Multiple* 

Phenytoin Sodium 

Phytonadione 

Piperacetazine 

Piperazine Citrate 

Pipobroman 

Potassium Aminosalicylate 

Potassium Chloride 

Pralidoxime Chloride 

Prednisolone 

Prednisolone Acetate 

Prednisolone Sodium Phosphate 

Prednisone 

Prilocaine Hydrochloride 

Procainamide hydrochloride 

Procaine Hydrochloride 

Procaine Merethoxylline; Theophylline 

Prochlorperazine Edisylate 

Prochlorperazine Maleate 

Progesterone 

Promazine Hydrochloride 

Promethazine Hydrochloride 

Propantheline Bromide 

Propoxyphene Hydrochloride 

Propoxyphene Hydrochloride; *Multiple* 

Propranolol Hydrochloride 

Propyliodone 

Propylthiouracil 

Protamine Sulfate 

Pseudoephedrine Hydrochloride 

280

Pseudoephedrine Hydrochloride; Triprolidine Hydrochloride 

Pyridoxine Hydrochloride 

Pyrvinium Pamoate 

Quinestrol 

Quinidine Gluconate 

Quinidine Sulfate 

Rescinnamine 

Reserpine 

Saralsin Acetate 

Secobarbital Sodium 

Selenomethionine, SE-75 

Sodium Iodide, I-123 

Sodium Iodide, I-131 

Sodium Monofluorophosphate 

Sodium Succinate 

Somatropin, Biosynthetic 

Streptomycin Sulfate 

Succinylcholine Chloride 

Sulfabenzamide; Sulfacetamide; Sulfathiazole 

Sulfadiazine 

Sulfameter 

Sulfamethizole 

Sulfamethoxazole 

Sulfaphenazole 

Sulfasalazine 

Sulfinpyrazone 

Sulfisoxazole Diolamine 

Sulfoxone Sodium 

Suprofen 

Technetium TC-99M Albumin Aggregated 

Technetium TC-99M Sodium 

Pertechnetate 

Temazepam 

Testolactone 

Testosterone Propionate 

Tetracycline Hydrochloride 

Thalidamide 

Theophylline 

Thioridazine Hydrochloride 

Thyroglobulin 

Timolol Maleate 

Tioconazole 

Tolazamide 

Tolbutamide 

Trazodone Hydrochloride 

Triamcinolone Acetonide 

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Triazolam 

Trichlormethiazide 

Triclofos Sodium 

Tridihexethyl Chloride 

Triflupromazine Hydrochloride 

Trihexyphenidyl Hydrochloride 

Trimeprazine Tartrate 

Trimethoprum 

Trimipramine Maleate 

Tripelennamine Hydrochloride 

Triprolidine Hydrochloride 

Trisulfapyrimidines 

Troleandomycin 

Ursodiol 

Verapamil Hydrochloride 

Veratrum Viride 

Vinblastine Sulfate 

Fincristine Sulfate 

Viomycin Sulfate 

Warfarin Potassium 

Warfarin Sodium 

Xenon, XE-133 

Some forms of these compounds were restricted after clinical trails 

showed them to be safe. There has been tremendous iatrogenic (doctor- 

induced) damage done to the people of the United States. Clinical drug 

trials are not at fault here, but the medical establishment’s worshipping 

of these clinical drug trials are. Every drug on this list went through the 

same clinical trials that the medical establishment uses as its criteria. 

This decision-making process of taking clinical trials and making them 

the demigod of the industry is at fault. People are being hurt because of 

faulty logic in medicine. These trials are expensive and can be purchased 

by rich patent-seeking synthetic chemical companies. This author 

realizes that challenging the establishment’s heart will not be taken 

lightly, and will not be without violent attacks. 

If the legal damages that have been incurred by these iatrogenic 

compounds are looked at, it is possible to see that there are literally 

billions of dollars every year paid out by drug companies in medical 

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malpractice and iatrogenic damage suits. The vast amount of damage 

caused by this industry is incredible; an industry which takes in 

approximately one hundred billion dollars of income pays out literally ten 

to twenty billion dollars a year in malpractice settlements. This still 

leaves an eighty billion dollar profit margin in an industry which spends 

very little in actual product manufacturing. The largest amount of 

expenditure by any drug company is that of research, development, and 

clinical trials of laboratory studies. 

It is this very research and development of the whole cognitive plan of 

allopathic medication that is being challenged. The allopathic medication 

philosophy is one that works against the body, or develops a compound 

to sedate a symptom. If the person has a histamine response, an anti- 

histamine is given; if the person has depression, an MAO inhibitor may 

be given. In every case of allopathic utilization, it is assumed that the 

body’s function is irregular and foolish, and some type of synthetic 

irregularity which can upset the cybernetic balancing system of the body 

develops. 

The legal issues of medical practice are also stacked against alternative 

practitioners. In 1990, of the 570,000 doctors in the United States, 1,437 

were put on probation, or had their licenses suspended or revoked. That 

represents .3% of the doctor population. In 1989, there were 1,500, and 

9 practitioners who were likewise reprimanded. Very few of these 

practitioners were actually prosecuted for unprofessional conduct by 

aligning themselves with alternative practices. The majority of these 

medical doctors were dealt with because of alcohol abuse, drug abuse, 

and sexual abuse of patients; some of them for allopathic malpractice. 

Very few of them were actually dealt with because of alternative theories. 

In most states, a medical doctor is bound to perform therapies and 

diagnostic techniques which are medically accepted. 

In 1990, the Alaska State Medical Board “may not base a finding of 

professional incompetence solely on the basis that a licensee’s practice is 

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unconventional or experimental in the absence of demonstrable physical 

harm to the patient.” Source: www.healthy.net/public/legal- 

lg/regulations/MPA.HTM) 

If the doctor is not hurting anybody with an experimental or 

unconventional technique, he/she would not have his license revoked. 

Strong evidence would have to be found that the patient had been 

harmed in order to challenge the doctor. Many of these so-called 

unconventional therapies are accepted by a vast majority of doctors, and 

there is no one form of medicine that is accepted above all others. 

Medicine abounds with many techniques that are not fully, scientifically 

evaluated or properly challenged. Oftentimes, doctors who use these 

unconventional techniques are challenged by traditional medical doctors 

on the basis of only one or two cases. Many doctors have had their 

practices disrupted because of one or two cases where unconventional 

therapy did not quite abate the patient’s complaint. 

Doctors see patients dying every day. Hospitals abound with patients 

whose therapies and diagnostic accuracy have led to their demise. Robert 

S. Mendelsohn, in his book, Confessions of a Medical Heretic, (Chicago: 

Contemporary Books. 1979), wrote that when the doctors in a group of 

hospitals in a certain local community went on strike, there was a major 

change in the death rate – it dropped dramatically. Fewer people died 

when doctors stopped practicing some accepted medical techniques. 

In another case in Denver, Colorado, the state charged parents for not 

using traditional medicine when their child died from a disease that was 

assumed to be treatable at a local hospital. The parent was a Christian 

Scientist who believed more in prayer than in drugs. If the ratio of 

children who survive with Christian Scientist parents vs. the ratio of 

children who survive overall in hospitals is looked at, there is a 

tremendous degree of variance. Children died at a greater rate in 

hospitals than they did from having Christian Scientist parents. In the 

world today, The United States is fifteenth overall in birth mortality, 

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meaning that there are fourteen countries where newborns have a better 

chance of survival than in the United States. These countries are those 

that depend more on natural medicine, homeopathy, and prevention 

techniques. Perhaps these types of analyses can open up the closed 

minds of the so-called traditional statisticians to realize that perhaps 

there is an alternative. 

Legal judgments can be based on incomplete scientific ideas. It must 

be accepted that the science of medicine is a pseudo-science; it is not an 

exact philosophy. With this in mind, we should be slow to write laws that 

prohibit or discourage different philosophies of medicine. 

Practitioners and patients have the right to make choices. Medical 

boards and peer groups are not needed to challenge practitioners who try 

to take philosophies and practices and push them into areas where they 

do not have strong scientific validity. The laws of each state for the 

practice of medicine are vital, and medical board inquiries are essential 

in developing better and better qualities of medicine. Yet in the proof that 

a doctor is doing something wrong with unconventional techniques, as in 

the case of Warren Levin, who was challenged because of two separate 

instances, it should become quickly apparent that one should not jump 

to conclusions on one or two cases of impropriety. No doctor in the land 

could withstand such a shifted bias. Whereas one or two cases out of the 

thousands seen over a ten-year period should put a person’s practice on 

the line. Statistics must be looked at as well, and looked at for a certain 

percentage, wherein a doctor might be brought out in front of a peer 

group, and the peer group also should be able to express different 

opinions. 

Many people with medical minds are firmly entrenched in 

reductionism, synthetic chemistry and surgery, who make tremendous 

amounts of money for the industries that they promote. Yet people die 

every day of iatrogenic diseases resulting from surgery and synthetic 

drugs. Society has found a way to let these doctors off the hook, and yet 

285

they put doctors who do unconventional therapies on the hook. It is 

possible that this challenge might be directed to help destroy a natural 

medicine industry which would challenge the incomes of the synthetic 

drug companies. 

Investigative books, including: Murder by Injection: The Story of the 

Medical Conspiracy against America, by Eustace Mullins (P.O. Box 1105, 

Staunton, Virginia 24401: National Council for Medical Research, 1988). 

Off the Pedestal: New women in the Art of Homer, Chase, and Sargent, 

edited by Holly Pyne Connor. New Brunswick, N.J.: Rutgers University 

Press, 2006, Mendelsohn’s series, and many others, are bringing to light 

the vast medical cover-up that has been promulgated by allopathic 

minds seeking to tyrannize and influence the minds of men. We need to 

deepen our philosophy of medicine, get into quantum physics, and try to 

understand biology at many different levels. These levels will include the 

ideas of statistical analysis, peer group philosophies, and scientific 

development of energetic phenomena. 

In the Quantum Biology Workbook, a heavy-duty physics statement is 

made using the highest levels of mathematics, physics and science 

known to our society. We conclude that allopathy is an irregular choice, 

and that the factors of clinical trials in reductionistic science are 

incomplete in their ability to protect the people using pharmaceutical 

products. We can see from this advanced physics and this upper level 

science that homeopathy and naturopathy are much more logical choices 

to use in developing medical techniques. 

As we go through different clinical trials that have been done in this 

book, we also review the literature of other research that has been done 

in naturopathy and homeopathy. We can see that in almost every 

attempt to utilize naturopathic and homeopathic techniques success is 

achieved. It is very rare in the literature to find a homeopathic or 

naturopathic study that failed to show a large degree of efficacy and 

safety. 

286

Jos Kleijnen, Paul Knipschild, and Gerben ter Riet, in their article in 

the British Medical Journal, Clinical Trials of Homeopathy, (BMJ 1991; 

302(6772), 316-323), assayed over 105 clinical trials of homeopathy from 

around the world. They concluded that 81 of the trials showed positive 

scientific undeniable results; 24 of them could be challenged. They 

concluded that there was a legitimate case for further evaluation. 

Full text article can be found at: 

www.pubmedcentral.nih.gov/picrender.fcgi?artid=1668980&blobtype=pdf 

According to the Null hypothesis in the case of homeopathy there is 

dramatic evidence of efficacy. Homeopathy works according to the 

scientific literature. With this type of data contained in these books and 

in this type of report it would seem that the use of homeopathy not only 

should be warranted, but that using an allopathic drug, which could 

produce a side effect or risk, might become a case of medical impropriety. 

I don’t believe that medicine can wait for homeopathy to be challenged 

over twenty years time. 

Homeopathy and naturopathy as an industry throughout the world 

outsell allopathic medications by almost three to one. This is because of 

the large amount of sales that are done in India, Pakistan, Bangladesh, 

China, etc. Out of this entire world market, which amounts to perhaps 

ten billion dollars in sales (it costs much less to manufacture and sell 

homeopathic products than allopathic ones), malpractice and different 

settlements measure in the thousands of dollars throughout the entire 

world. There are hardly any suits against naturopathic and homeopathic 

doctors, although when this does happen they are usually very small. 

Out of a ten billion dollar industry, less than one percent of one percent 

of one percent of one percent of its total capital generation is paid out in 

malpractice, compared to our allopathic counterparts, who pay in the 

neighborhood of fifteen to twenty percent a year in settlements. 

The justification for homeopathy need not come completely from 

clinical trials. Without using clinical trials it’s possible to look at the 

287

world market and see that homeopathy works. It makes sense. One can 

look at the returns on malpractice insurance which shows how many 

people were hurt, and see that homeopathy works, whereas synthetic 

chemistry hurts. The statistics bear this out. One can look at these 

statistics and see that allopathy needs to be challenged, and that the 

process of using clinical trials and revering the publication/print process 

as the end all answer must be challenged in order to proceed any further 

with medicine. Reductionistic clinical trials are the problem, not the 

solution. 

It must be realized that the mind of the observer interferes with the 

experiment. This is a basic premise of quantum theory which allopathy is 

not putting into use. The basic treatise of this book has proven that 

quantum theory must be considered as a meaningful step into biology. 

In quantum theory, the mind state of the observer will influence the 

outcome. In the preparation of clinical trials, the power of mental 

philosophy and the mind state of the person behind them must be 

recognized. The development of modern chemistry, which pinnacled in 

synthetic processes, gave these people a severe mind set, a mind set 

based on chemical analysis, not energy, physics, and other sciences. This 

predominantly chemical-based philosophy will interfere with their 

observational ability. Hence, it is possible to see the action of this 

philosophical backdrop in their pursuit of medical truth. This has led to 

chemical solutions, surgical solutions, and allopathic ideation. 

Another philosophical and psychological problem behind this medical 

juggernaut is the idea of allopathic superiority to nature. As was pointed 

out in Quantum Biology, it is basically akin to the philosophy of allopathy 

and synthetic chemicals that the observer knows more than the situation 

he or she observes, in that the medical doctor knows more about biology 

than the patient’s body. The patient’s body, thus, becomes flawed and 

stupid in the eyes of the experimenter. If there is a histamine reaction, 

an anti-histamine is given to the “stupid body”; if there is depression, the 

288

“stupid body” is given an MAO inhibitor; if there is fever, the “stupid 

body” is given an anti-pyretic. In other words, the concept of allopathy is 

that something is wrong with the body and that outside intervention 

from a superior intellectual source will help correct the problem. This 

also is a seriously flawed philosophy and psychological backdrop to 

which all of the medical experiments are then interred. 

With homeopathy and naturopathy as a basis in medicine, we can 

develop a different foundation. Our foundation will revere the natural 

process, and realize our inability to know intimately such a process. We 

would want to intervene on the process very little, and try to stimulate 

the process back to its own natural balance using natural mechanisms 

and gentle nudges to help stimulate the organism to achieve its own 

balance. The organism has the superior knowledge of biology. 

If we take such a philosophy, and reevaluate the last hundred years of 

medical research, we can see that some of the conclusions drawn from 

allopathy were severely flawed. An overview of the medical research will 

show us that many of the experiments performed were reductionistic and 

philosophically inadequate. 

Part of this book has been written with the idea that there is an 

evolution in human thought, and that human thought has evolved from 

many different states. It is wrong for us to think that human thought 

and social conditions have stayed the same through the years. The early 

tribes and societies had very weak ideas of philosophy and the ideation of 

a king becoming part god showed some of the limitations of their 

thinking. Early societies did not have the ideation of spatial organization 

to allow them to do proper art perspectives. This was a developmental 

process. There was a developmental process in the ideas of psychology 

and philosophy, in the idea of science, and in the concepts of religion 

and theology. 

Every form of human thought will evolve and change through the ages, 

just as medicine will evolve and change through the impact of this book 

289

and thousands more like it. They will challenge the ideas behind medical 

thought and philosophy and bring about new ones that include a soft 

approach, and a gentleness and humility toward what is not known. As 

we develop and achieve this new type of mental thought we will be able to 

embrace an old philosophy of medicine. We will be able to find this old 

philosophy, ignored by technology and achieve a new way. The thesis 

and the antithesis will blend into a new form of truth. The thesis is that 

of naturopathy and homeopathy; the antithesis is allopathy and surgery. 

These two will blend to achieve a new form of thought in which the 

doctor, being educated and knowledgeable in all of these different 

philosophies will have more directed choices, and will be able to affect 

more safety and efficacy with his patients. 

It is this author’s purpose to challenge the conclusion of the article in 

the U.S. News and World Report. Perhaps more long-term studies need to 

be adapted to allopathic thought (long-term meaning over a period of ten 

generations). To say that more clinical trials need to be done in 

homeopathy is to state a truth, but to say that before homeopathy 

should be used by the masses, this needs to be done is to state an 

untruth. Grossly incorrect is this proposition to make homeopathy spend 

massive amounts of money on ridiculous reductionistic trials. 

Homeopathy is a legal entity in America and should not be forced into 

major expenditures in clinical trials which would do nothing to increase 

safety or efficacy. It is the opinion of these synthetic drug companies that 

if they could force homeopathy into such trials, they could perhaps 

destroy homeopathy, because it does not make the large amounts of 

money that allopathy does. Homeopathy would not have the money to 

afford such trials. Homeopathy by definition is not a money-making 

proposition. It is, however, curative. 

These trials are irregular with modern mathematics and modern 

medicine, and they will not give us the complete results we thought they 

would. Statistics lie, and statisticians deceive. 

290

The FDA was formed by Dr. Clayton to protect homeopathy. He lobbied 

for years and years for a federal organization that could protect the 

American people in their choices of food and drugs. He sought to help in 

protecting the philosophy of homeopathy. Within two weeks after 

founding the FDA, Dr. Clayton died. The FDA has acknowledged the 

Homeopathic Pharmacopeia of the United States, and it is a legally 

accepted in America. The Homeopathic Pharmacopeia of the United 

States (HPUS) has never commanded enough money to generate 

popularity. 

Allopathic philosophy and its use of clinical trials have sought to 

tyrannize people’s minds and change their perspectives. It has hoped 

that doctors would make allopathic choices of drugs, rather than 

homeopathic choices. This type of tyranny over the minds of people is 

what the founders of our country sought to defend against. 

In 1991, President George W. Bush developed a thyroid condition which 

produced heart palpitations. This author wrote him a letter. In that 

letter, I said (in paraphrase): 

Mr. President: 

As President of the United States, I recognize that you have a 

lot of pressure to choose an allopathic therapy for your 

condition. At this time of war, (written just after the Gulf War), I 

can imagine the tremendous amount of stress and tension that 

you were going through, and I can also fathom how it has 

probably produced a hyperthyroid condition that has now gone 

out of control. In your choice of therapy, Mr. President, you as 

an American citizen have the right to choose many different 

types of medicines. 

Your can choose chiropractic treatment for your condition, 

and perhaps adjustment of the nerves might provide a balance 

to the thyroid and alleviate stress. You can choose acupuncture 

treatment, and an acupuncturist might try to balance the 

meridian flow and help to sedate the irritation of the nerves of 

the heart, and sedate the body and balance its energies. You 

can choose nutrition, and seek a diet to help relax and balance 

291

your metabolism. You can also choose homeopathic therapy, 

and take a homeopathic which we have shown to be not only 

safe, but also effective in many cases of treating hyperthyroid 

conditions. You could choose naturopathy in the District of 

Columbia, and seek natural therapies for your condition. You 

also can choose allopathic medicine, which works against the 

body. I realize, Mr. President, the tremendous amount of 

pressure on you to choose allopathic medication. Because of 

your position as United States President, if you were to choose a 

chiropractor, acupuncturist, homeopath, or other doctor, you 

might rock a very large economic boat, and threaten an 

entrenched philosophy of medicine. 

The Queen of England, in a very similar position, has made 

the choice of homeopathy, Mr. President. She, The Queen of 

England and her family are only treated by homeopathic 

physicians; they are not treated in allopathic ways at all. They 

have rocked the big boat for many, many years. Even in light of 

extreme pressure, the logic and success of homeopathy 

outweighs the finances of allopathy. 

Along with this letter, I send two bottles of Hyperthyro-1 

homeopathic which we were able to blend. We did some pilot 

studies and found that it was safe and effective in these cases. 

Many similar cases of hyperthyroidism have been cured by this 

remedy. 

So, Mr. President, you as an American citizen have the 

freedom of choice, to choose any of these different endeavors. I, 

as an American citizen have the freedom of choice, to write this 

letter, and to voice what type of therapy I might have chosen. 

Had I been in your position, Mr. President, I would have chosen 

homeopathy and alternative natural therapies. [President Bush 

could also have chosen naturopathic treatment, since 

naturopathy is legal within the confines of Washington, D.C.] 

But also, Mr. President, as an American citizen I will fight for 

you to have the right to choose. If you choose allopathy, even if I 

don’t agree or approve, I will fight to protect that choice. I hope, 

Mr. President that you will also fight to protect my choice. There 

are several forces in the allopathic community who so value 

clinical trails, and so value their process and their philosophy 

that they seek to tyrannize the minds of men. And Mr. 

President, you can walk down to the Jefferson Memorial, where 

written around the top of the inside of the memorial, in big 

letters carved in stone, is a quote by Thomas Jefferson: “I have 

292

sworn on the altar to oppose any tyranny over the minds of 

men.” Mr. President, freedom of choice has never been more 

threatened than it is now by allopathic mental tyranny. 

Homeopathy entered into 1992 with some baggage as well. The people 

doing homeopathy in the United States were, most of the time, unable 

and unwilling to do highly sophisticated quality control. Oftentimes, the 

manufacturers did not comply with legal regulations set out by the FDA. 

Even the 211 CFRs (Code of Federal Regulations) were not utilized by 

unregistered homeopathic companies. Homeopathy must build quality 

control techniques such as those used at Dr. Recommends; pilot studies, 

clinical trials, safety and effectiveness analysis, culture techniques, and 

chromatography. Quality control techniques of the energetic process 

must be done as well, such as the REGAE (Rare Electron Gas Allopathic 

Evaluation) capacitance rating, inductance rating, conductance rating, 

and polymorphic shaping studies to understand the crystalline effects. 

These are some of the techniques that must be done in a true quality 

control way, as well as total legal compliance. As yet, the homeopathy 

industry as a whole does neither. To meet the challenge of our new 

thinking, and to direct homeopathy back into the medical mainstay, it 

will have to meet these challenges head on, change, and bring itself into 

reputability. 

As we have seen from our exploration, reductionism was probably more 

of a problem than a solution in science. We need to use our 

reductionistic trials; we also need to develop holistic, individualized 

concepts of medicine for more safety and effectiveness without just using 

short-term clinical trials. Nature knows protection. We only hope that the 

freedom of choice be kept alive in America. Many people I have known 

have left America in search of freedom of medical choice. We can only 

hope that freedom of choice be reestablished as the basic tenet of the 

American justice system. Our capitalistic philosophy has produced a 

successful past for our patentable, synthetic, chemical brethren. But 

293

now the logic and reason of homeopathy and naturopathy must earn at 

least the freedom of choice. Perhaps this philosophy will earn more. As 

Victor Hugo once said, “There is only one thing more powerful than all 

the armies of the world, and that is an idea whose time has come.” 

Natural medicine’s time has come. Watch out, allopathy. 

Deepak Chopra’s book, Quantum Healing: Exploring the Frontiers of 

Mind/Body Medicine, New York: Bantam Books, 1989, offers supportive 

information for what is discussed here. He speaks of the idea of quantum 

healing which must involve compassion, and a new form of 

understanding that goes beyond the physical area into quantic 

dimensions. This is very important for us to realize. In his book, he 

makes a point about how a certain patient was “picnic-deficient,” and 

needed to have nice, enjoyable picnics to restore him to health. Chopra 

puts into view a mystical connection with another world, and explains it 

in different Asian terms. These terms he later relates to as quantum 

factors of types of energy. 

In our treatise, we also find that there is something that affects this 

indeterminacy, or quantic principle. We have called it a “God 

Consciousness,” a nature within Quantum Biology. We truly believe that 

Chopra’s referral to a God Consciousness and a quantic understanding 

is the same as what we are implying. There must be some type of greater 

power that dictates the precision with which biology pursues. 

Chopra puts some of our scientific perspectives into more human 

terms as he relates different cases, and how the cases go beyond classic 

medical understanding. Many other researchers of late have followed a 

similar path, and found challenging ways of critiquing modern medicine’s 

statistical type of logic. We must point out in this document that if there 

is a God Consciousness, an ability of will, happiness, joy, compassion, 

caring, sharing and touch to help people, it will not fit into any model 

that could be measured with statistical pre-test/post-test, clinical, drug 

trial data. Clinical trials need to be part of our concept, but not deified. 

294

We need to use them to help determine safety and help to interpret our 

range of effectiveness, but they still should be within the guidelines of 

nature. 

PROBLEMS BEHIND THE MEDICAL DILEMMA 

� Arrogance; a belief in superiority over biology 

� Persecution for the belief in nature and homeopathy 

� Judgmentalism; psychological over-reaction against other natural 

philosophies. Preferred doctors of high influence are almost always 

allopaths who are ignorant of homeopathy 

� Greed; synthetic companies profit mostly from patented unnatural 

compounds 

� Lack of personal responsibility in healthcare 

� Belief that medical technology will save someone after years of an 

unhealthy lifestyle 

� Crisis philosophy; seeking medical help only after all else fails 

� Insurance costs 

� Malpractice costs and medical fears 

� Lack of a true biology and no philosophical base 

� Quantity based medicine, not quality based 

295

SOLUTIONS TO THE MEDICAL DILEMMA 

� Humility, reverence for nature’s process, understanding of 

quantic philosophy 

� Proper study will show homeopathic and naturopathic 

credibility 

� Proper peer group process: allowing a group of like-minded 

doctors to evaluate the amount of harm done, if any 

� Protecting natural formulas with more strict copyrights that 

allow natural based pharmaceutical companies to benefit from 

their research 

� Building personal responsibility into medical education at every 

level 

� Educating for prevention and early treatment procedures 

� Building a low-cost system of wellness counselors who can 

intervene and help in early and simple health care problems, 

reserving doctors and hospitals for crisis care 

� Reducing insurance costs by using homeopathy and 

naturopathy and also escalating insurance costs for: 

Obesity 

Smoking 

Alcohol abuse 

Drug addiction 

Letting the ones who incur the most medical costs pay them. 

This will discourage bad health habits. 

� Malpractice results mostly from synthetic allopathic drugs and 

surgery. Changing to homeopathy and naturopathy will show 

dramatic results. 

� Appreciation and reverence for the unknown builds a quantum 

philosophy for medicine. 

� Building everything for quality, not quantity. This will take more 

cash initially, but will be cheaper in the long run. 

296

Now, let us be more specific as to what might be needed to actually set 

the criteria of how to approve new combination homeopathics, or new 

combination drugs. First, we will need to depend on safety as our 

primary goal. We need to look for safety first, or as Hippocrates said, 

“First, don’t hurt.” This needs to be our absolute guideline for everything 

we do. We have to imagine that everything we do could get to the youth 

of our society, as I think that everything could get to my five year old 

daughter. The thought of anything happening to this small child is 

absolutely, totally intolerable. First don’t hurt. 

Safety first is an absolute guideline. It is unfortunate that in the late 

1950s the president of the American Medical Association (AMA), said in a 

public address that the AMA no longer had to guarantee safety first; they 

had to biopsy, x-ray, sedate, stimulate, stab, cut, and otherwise defame 

the body in order to do medicine. This idea will be intolerable in our new 

medicine as it forms. Safety first must be insured every step of the way. 

In a recent report, it was said that there is a possibility that the 

plankton at the South Pole might be in a condition of iron deficiency, and 

that if the plankton had an exposure to iron, they might be able to 

develop the ozone needed to compensate for the ozone deficiency of the 

South Pole. His treatise makes very sound, scientific sense, and all the 

science regarding the plankton around the South Pole has been done in 

a superior manifest way. But yet, the scientific community is hesitant to 

make such a maneuver, fearing the consequences of what one tanker- 

load of iron might do at the South Pole. 

This same type of fear of what this might do to the ecology of the entire 

world is not shared by the synthetic chemical companies, as they engage 

ever increasing numbers of synthetic chemicals that do not exist in the 

world, and they are putting these into the exosphere of our planet. This 

has been happening for over fifty years. Our new medicine will absolutely 

insist on proof that safety within the smallest amount of parameters 

must be guaranteed before we can proceed. We should no longer dump 

297

synthetic, never-occurring un-natural compounds into the environment 

in the percentage that they have been in the past. 

We must set policies as to what we are going to do, and this policy has 

to be geared through the idea that only nature knows. Only through 

such humility can science actually address the issues of biology and 

medicine. The arrogant idea that if, “we do not know its function we 

should cut it out”, allowed for the destruction of adenoids, tonsils, 

appendix, spleen, thymus, etc. This type of arrogance must cease. Nature 

knows, and nature had a plan for the adenoids, tonsils and appendix, 

even though we did not know it. To assume that it is not needed because 

we do not understand it, is the absolute arrogance of science. We must 

have humility and a reverence towards science to be able to proceed in 

any way, shape or form. Clinical trials are not enough; we must have a 

guaranteed policy of understanding nature and nature’s own in order to 

proceed into the new dimensions of medicine and biology 

The alternative industry has done very little to offer any type of 

scientific inquiry regarding statistics as its guideline. We will need to 

develop pilot studies that guarantee effectiveness in safety, primarily. 

These types of statistical endeavors will have to be replicated by many 

different doctors in many different ways; not with the same criteria as 

drug trial studies, but in something similar that will guarantee the 

world’s safety and the world’s effectiveness of such remedies. These pilot 

studies need to use the statistics of the day, and will have to be at a 

razor-sharp edge to prove safe and effective. 

As we continue to revere nature, and understand that only nature truly 

knows, we will have to develop this into a hallmark of our biology. This 

will allow homeopathy and all its nosodes, allersodes isodes, sarcodes, 

etc., to explode into the scene of medicine. We also need to have the 

philosophy and the psychology to understand that behavioral medicine, 

psychological intervention, the psycho-immunological link and other 

factors are also very much needed for us to have a true medicine. We 

298

need to take Chopra’s advice, and develop a science and a medicine of 

compassion, caring, sharing, touch, and healing to carry us into the new 

era of medicine. 

We will need to have a constant field input to allow doctors who are 

using such medications to critique their actions in an ever changing 

environment, realizing that what the action of any homoeopathic or drug 

might be might change as the population evolves, in light of an ever 

changing reactivity to the environment. Statistics will play an ever larger 

part, but yet will not be deified in light of philosophy. The philosophy 

that nature knows must be revered, not the statistics of clinical trials. 

We must realize what nature and God Consciousness can do in the 

field of biology and medicine. Only then, can we truly shape a new 

medicine through these different guidelines, concentrating on safety at 

all costs. We need effectiveness, but never at the cost of safety; revering 

nature and education, so that the doctors, the populace, the society at 

large can share in our appreciation and harmony of the natural flow of 

medicine. To this end this book is written. 

299

SUMMARY 

� A review of the insurance literature and true success stories on 

naturopathy and homeopathy vs. synthetic allopathy have 

conclusively proven that there is a severe problem in the field of 

synthetic allopathy. Synthetic allopathy pays billions of dollars in 

damages each year. Millions more are hurt by this technology who 

do not seek damages. Those who are helped do not outweigh the 

damages. The solution for this could be the new wave of 

homeopathy and naturopathy into general areas of medicine. 

� There were profiteering issues behind the surge of synthetic 

allopathy that were spearheaded by reductionism as a mechanism 

of directing research. Now with the skills developed through 

mathematics and quantum theory, it is possible to see that the 

field of reductionistic research leaves dramatic problems for 

medicine. 

� A new system of research must be developed for medicine. Some 

ideas for a new system were presented within this chapter. 

� Medicine must learn not to deify statistical reductionistic papers, 

and must learn to develop a reverence for the natural process 

rather than synthetic dynamics. 

� Freedom of choice must return to the world system of medicine. 

� Systems of medicine such as chiropractic, naturopathy, 

homeopathy, acupuncture, behavioral medicine and biofeedback 

are legal systems. 

� Synthetic allopathy seeks to tyrannize the minds of men against 

these other medical beliefs. 

� We must oppose any such tyranny over the minds of men. 

300

METABOLIC PATHWAYS 

This section includes a list of the cellular energy components utilized 

in cellular metabolism and energy regulation. Sometimes an irregularity 

of function can be corrected with a homeopathic of the enzyme or 

component. 

Alcohol dehydrogenase 

Glycerol-3-phosphate dehydrogenase 

D-Xylulose reductase 

L-Xylulose reductase 

D-Iditol dehydrogenase 

Glucuronate reductase 

UDP glucose dehydrogenase 

Histidinol dehydrogenase 

Shikimate dehydrogenase 

Lactate dehydrogenase 

D-Lactate dehydrogenase 

Glycerate dehydrogenase 

3-Hydroxybutyrate dehydrogenase 

3-Hydroxyisobutyrate dehydrogenase 

Mevaldate reductase 

Hydroxyethylglutaryl-CoA reductase (NADPH) 

3-Hydroxyacyl-CoA dehydrogenase 

Malate dehydrogenase 

Malate dehydrogenase (oxaloacetate-decarboxylating) 

Malate dehydrogenase (decarboxylating) 

Isocitrate dehydrogenase (NAD+) 

Phosphogluconate dehydrogenase 

Phosphogluconate dehydrogenase (decarboxylating) 

L-Gulonate dehydrogenase 

Glucose-6-phosphate dehydrogenase 

Ribitol dehydrogenase 

3-Hydroxpropionate dehydrogenase 

Tartronate-semialdehyde reductase 

Glyoxylate reductase (NADP+) 

Hydroxypyruvate reductase 

Malate dehydrogenase (NAPD+) 

Phosphoglycerate dehydrogenase 

3-Oxo-[acyl-carrier-protein] reductase 

Retinol dehydrogenase 

IMP:NAD+oxidoreductase 

301

L-Gulonolactone oxidase 

Choline dehydrogenase 

Glycerol-3-phosphate dehydrogenase 

Aldehyde dehydrogenase 

Benzaldehyde dehydrogenase (NADP+) 

Betaine-aldehyde dehydrogenase 

Aspartate-semialdehyde dehydrogenase 

Glyceraldehyde-phosphate dehydrogenase 

IMP dehydrogenase 

Succinate-semialdehyde dehydrogenase (NAD (P) +) 

Malonate semialdehyde dehydrogenase (acetylating) 

Glycoadehyde dehydrogenase 

Succinate-semialdehyde dehydrogenase 

2-Oxiosovalerate dehydrogenase 

Benzaldahyde dehydrogenase (NAD+) 

Aminoadipate-demialdehyde dehydrogenase 

Aminomuconate-semialdehyde dehydrogenase 

Retinal dehydrogenase 

Xanthine dehydrogenase 

Glutamate-semialdehyde dehydrogenase 

Xanthine oxidase 

Pyruvate dehydrogenase (lipoamide) 

2-Oxobutyrate synthase 

Dihydrouracil dehydrogenase (NAD+) 

Dihydrouracil dehydrogenase (NADP+) 

Acyl-CoA dehydrogenase (NADP+) 

Enoyl-[acyl-carrier-protein] reductase 

Enoyl-[acyl-carrier-protein] reductase (NADPH) 

Prephenate dehydrogenase (NADP+) 

Orotate reductase 

Coproporphyrinogen oxidase 

Succinate dehydrogenase 

Butryl-CoA dehydrogenase 

Acyl-CoA dehydrogenase 

Glutaryl-CoA dehydrogenase 

Alanine dehydrogenase 

Glutamate dehydrogenase 

Serine dehydrogenase 

Valine dehydrogenase (NADP+) 

Leucine dehydrogenase 

D-aspertate oxidase 

L-amino acid oxidase 

Glycine dehydrogenase 

Amine oxidase (pyridoxal-containing) 

Ethanolamine oxidase 

Pyrroline-2-carboxylate reductase 

302

Pyrroline-5-carboxylate reductase 

Saccaropine dehydrogenase (NAD+, lysine-forming) 

Saccharopine dehydrogenase 

L-Pyrroline-5-carboxylate dehydrogenase 

Sarcosine oxidase 

Sarcosine dehydrogenase 

Dimethyglycine dehydrogenase 

L-Pipecolate dehydrogenase 

Cystine reductase (NADH) 

Dihydrolipoamide reductase (NAD+) 

Hypotaurine dehydrogenase 

Sulphite oxidase 

Sulphite reductase (ferredoxin) 

L-Ascorbate-cytochrome b5 reductase 

Ascorbate oxidase 

Catechol 1, 2-dioxygenase 

Catechol 2, 3-dioxygenase 

Homogentisare 1, 2-dioxygenase 

3-Hydroxyanthranilate 3, 4-dioxygenase 

Tryptophan 2, 3-dioxygenase 

Cycsteine dioxygenase 

B-Carotene 15, 15’ –dioxygenase 

4-Hydroxphenylpyruvate dioxygenase 

myo-Inositol oxygenase 

Benzoate 1, 2-dioxygenase 

Y-Butyrobetaine-2-oxogluterate dioxygenase 

Proline, 2-oxogluterate dioxygenase 

Trimethylysine, 2-oxogluterate dioxygenase 

Anthranilate 1, 2-dioxygenase (deaminating, decarboxylating) 

Imidazoleacetate 4-monooxygenase 

Kynurenine 3-monooxygenase 

Phenylalanine 4-monooxygenase 

Tyrosine 3-monooxygenase 

Monophenol monooxygenase 

Prostaglandin synthase 

Acyl-CoA desaturase 

Squalene monoxyenase (2, 3-epoxidising) 

Ribonucleoside-diphosphate reductase 

Nicotinamide methyltransferase 

Guanidinoacetate methyltransferase 

Dimethylthetin-homocysteine methyltransferase 

Acetylserotonin methyltransterase 

Betaine-homocysteine methyltransferase 

Homocysteine methyltransferase 

Tetrahydropteroyltriglutamate methyltransferase 

Phosphatidylethanolamine methyltransderase 

303

Glycine methyltransferase 

Noradrenaline N-methyltransferase 

Thymidylate synthase 

Serine hydroxymithyltransferase 

Phosphoribosyglycinamide formyltransferase 

Phosphoribosylaminoimidazole-carboxamie formyltransferase 

Glutamate formiminotransferase 

Methylmalonyl-CoA carboxyltransferase 

Aspartate carboamoyltransferase 

Ornithine carbamoyltransferase 

Glycine amidinotransferase 

Transketolase 

Transaldolase 

Amino-acid acetyltransferase 

Glucosaminephosphate acetyltransferase 

Arylamine acetyltransferase 

Choline acetyltransferase 

Phosphate acetyltransferase 

Acetyl-CoA acetyltransferase 

Dihydrolipoamide acetyltransferase 

Glycerophosphate acyltransferase 

Acetyl-CoA acyltransferase 

Diacylglycerol acyltransferase 

Carnitine palmitoyltransferase 

Lysolecithin acetyltransferase 

Sphingosine acyltransferase 

Lysine acetyltransferase 

Glutamate acetyltransferase 

S-Aminolaivulinate synthase 

[Acyl-carrier-protein] acetyltransferase 

[Acyl-carrier-protein] malonytransferase 

3-Oxoacyl-[acyl-carrier-protein] synthase 

Serine palmitoyltransferase 

1-Acylglycerolphosphate acyltransferase 

Phosphorylase 

Amylosucrase 

Glycogen (starch) synthase 

Sucrose synthase 

Glucuranosyl-transferase 

Starch synthase 

Lactose synthase 

Sphingosine B-galactosyltransferase 

Cellulose synthase (GDP-forming) 

Glucomannan 4-B-D-mannosyltransferase 

UDP galactose-N-acylsphingosine galactosyltransferase 

UDP-N-Acetylglucosamine glycoprotein N-acetyl-glucosaminyltransferase 

304

UDP galactose-ceramide galactosyltransferase 

GDP-fucose-lactose fucosyltransferase 

Purine nucleoside phosphorylase 

Pryimidine-nucleoside phosphorylase 

Thumidine phosphorylase 

Hypoxanthine phosphoribosyltransferase 

Uracil phosphoribosyltransferase 

Orotate phosphoribosyltransferase 

Nicotinate phosphoribosyltransferase 

Amidophosphoribosyltransferase 

ATPP-phosphoribosyltransferase 

Anthranilate phosphoribosyltransferase 

Nocotinatemonomucleotide pyrophosphorylase (carboxylating) 

Dimethyltransferase 

Methionine adenosyltransferase 

Geranyltransferase 

Amonopropyltransferase 

Farnesyltransferase 

Spermine synthase 

Aminotransferase 

Aspartate aminotransferase 

Alanini aminotransferase 

Glycine aminotransferase 

Tyrosine aminotransferase 

Leucine aminotransferase 

Histidinol-phosphate aminotransferase 

Acetylornithine aminotransferase 

Ornithine-oxo-acid aminotransferase 

Glutamine fructose 6-phosphate aminotransferase 

Succinyl-diaminopimelate aminotransferase 

B-Alanine-pyruvate aminotransferase 

Aminobutyrate aminotransferase 

L-3-Aminoisobutyrate aminotransferase 

4-Hydroxyglutamate transaminase 

Tryptophan aminotransferase 

Valine-isoleucine aminotransferase 

L-Lysine 6-aminotransferase 

2-Aminoadipate aminotransferase 

Branched-chain-amino-acid aminotransferase 

Serine-pyruvate aminotransferase 

Phosphoserine aminotransferase 

Glutamate synthase 

Glucokinase 

Ketohexokinase 

Fructokinase 

Galactokinase 

305

Mannokinase 

6-Phosphofructokinase 

Ribokinase 

Ribulodinase 

Xylulokinase 

NAD+kinase 

Dephospho-CoA kinase 

Triokinase 

Glycerol kinase 

Glycerate kinase 

Choline kinase 

Pantothenate kinase 

Pantetheine kinase 

Mevalonate kinase 

Homoserine kinase 

Pyruvate kinase 

D-Ribulokinase 

L-Xylulokinase 

N-Acylmannosamine kinase 

myo-Inositol-kinase 

Shikimate kinase 

Pyrophosphate-serine phosphotransferase 

Acetate kinase 

Phosphoglycerate kinase 

Aspartate kinase 

Formate kinase 

Carbamoyl-phosphate synthase (glutamine) 

Creatine kinase 

Phosphomevalonate kinase 

Nucleoside-phosphate kinase 

Nucleosidediphosphate kinase 

dTMP kinase 

Cytidylate kinase 

Phosphoglucomutase 

Acetylglucosamine phosphomutase 

Phosphoglycerosmutase 

Ribosephosphat pyrophosphokinase 

Pantetheinephosphate adenylyltransferase 

RNA nucleotidyltransferase 

DNA nucleotidyltrnasferase 

Glucose-1-phosphate guanylyltransferase 

Ethanolaminephosphate cytidylyltransferase 

Galactose-1-phosphate uridylyltransferase 

Hexose-1-phosphate guanylyltransferase 

GTP-mannose-1-phosphate guanylyltransferase 

Ethanolaminephosphate cytidylyltransferase 

306

Cholinephosphate cytidylyltransferase 

Nicotinatemononucleotide adenylyltransferase 

Mannose-1-phosphate guanylyltransferase 

UDP acetylglucosamine pyrophosphorylase 

Glucose-1-phosphate thyidylyltransferase 

Glucose-1-phosphate guanylyltransferase 

Phosphatidate cytidylyltransferase 

Acylmeuraminate cytidylyltransferase 

Ethanolaminephosphotransferase 

Cholinephosphotransferase 

Ceramide cholinephosphotransferase 

Blycerophosphate phosphatidyltransferase 

CDP diglyceride-serine o-phosphatidyltransferase 

CDP diglyceride-inositol phosphatidyltransferase 

Phospho-N-acetylmuramoyl-pentapeptide transferase 

Propionate CoA-transferase 

3-Oxoacid CoA-transferase 

3-Oxoadipate CoA-transferase 

Triacylglycerol lipase 

Phospholipase A2 

Lysophospholipase 

Acetylcholinesterase 

Aldonolactonase 

3-Oxoadipate enol-lactotase 

Acylcarnitine hydrolase 

6-Phosphogluconolactotase 

Phospholipase A1 

Acetyl-CoA hydrolase 

3-Hydroxyisobutyryl-CoA hydrolase 

Phosphoserine phosphatase 

Phosphatidate phosphatase 

5’ –Nucleotidase 

Glucose-6-phosphatase 

Hexosediphosphatase 

Histidinolphosphatase 

1L-myo-Inositol-1-phosphatase 

Phosphatidylglycerophospatase 

N-Acylneuraminate-9-phosphatase 

Nucleotidase 

Glycerophosphinicochopane diesterase 

Phospholipase C 

Phospholipase D 

Phosphatidylinositol phosphodieterase 

Sphingomyelin phosphosphesterase 

B-galactosidase 

B-fructofuranosidase 

307

Adenosylhomocysteinase 

Asparaginase 

Glutaminase 

Ureidosuccinase 

Formylaspartate deformatase 

Aryl-formamidase 

Acetylornithine deacetylase 

Glutaminase 

Ureidosuccinase 

Formylaspartate deformatase 

Aryl-formamidase 

Succinyl-diaminopimelatase desuccinylase 

Citrullinase 

Pantothensase 

Acylsphingosine deacylase 

Hippurate hydrolase 

Dihydropyrimidinase 

Dinydor-orotase 

Allantoinase 

Imidazolonepropionase 

Arginase 

Formiminoaspartate deiminase 

Arginine deiminase 

AMP deaminase 

IMP cyclohydrolase 

dCMP deaminase 

Phosphoribosyl-AMP cyclohydrolase 

Adenosinetriphosphatase 

Nucleoside triphosphatase 

Fumarylaetoacetase 

Kynureninase 

Phosphoamidase 

Carboxylyase 

Pyruvate decarboxylase 

Oxaloacetate decarboxylase 

Acetoacetate decarboxylase 

Aspartate 4-decarboxylase 

Glutamate decarboxylase 

Ornithine decarboxylase 

Diaminopimelate decarboxylase 

Phosphoribosylaminoimidazole carboxylase 

Histidine decarboxylase 

Orotidine-5’ –phosphate decarboxylase 

Aromatic –L-amino-acid decarboxylase 

Cysteine sulphinate decarboxylase 

Phosphoenolpyruvate carboxylase 

308

Di-phosphomevalonate decarboxylase 

Keto-L-glutonate decarboxylase 

Phosphopantothenoyl-cysteine decarboxylase 

Uroporphyrinogen decarboxylase 

Phosphoenolpyruvate carboxykinase (pyrophosphate) 

Ribulosebisphosphate carboxylase 

Propionyl-CoA carboxylase 

Phenylpyruvate decarboxylase 

Aminocarboxymuconate-semialdehyde decarboxylase 

Tartronate-semialdehyde synthase 

Indole-3-glycerol-phosphate synthase 

Phosphoenolpyruvate carboxykinase (ATP) 

Phosphatidylserine decarboxylase 

Aldehyde lyase 

Phosphoketolase 

Ketopantoaldolase 

Fructose-bisphosphate aldolase 

Phospho-2-keto-3-deoxy-heptonate aldolase 

Isocitrate lysase 

Malate synthase 

Hydroxymithylglutaryl-CoA lyase 

Citrate (si) –synthase 

ATP citrate (pro-3S)-lyase 

4-Hydroxy-2-oxoglutarate aldolase 

Acetolactate synthase 

N-Acylneuraminate-9-phosphate synthase 

Homocirtate synthase 

Anthranlate synthase 

Tryptophanase 

Fumarate hydratase 

Aconitate hydratase 

Citrate dehydratase 

Dihydroxyacid dehydratase 

5-Dehydroquinate dehydratase 

Enolase 

Phosphogluconate dehydratase 

L-Serine dehydratase 

Threonine dehydratase 

Enoyl-CoA hydratase 

Methylglutaconyl-CoA hydratase 

Imidazoleglycerolphosphate dehydratase 

Tryptophan synthase 

Cystathionine B-synthase 

Porphobilinogen synthase 

Mesaconate hydratase 

dTDP glucose 4, 6-dehydratase 

309

GDP-manose 4,6-dehydratase 

Urocanate hydratase 

Prophenate dehydratase 

Dihydrodipicolinate synthase 

3-Hydroxyoctanoyl-[acyl-carrier-protein] dehydratase 

D-3-Hydroxydecanoyl-[acyl-carrier-protein] dehydratase 

Threonine synthase 

Cystathionine Y-synthase 

Aspartate ammonia-lyase 

Methylaspartate ammonia-lyase 

Histidine ammonia-lyase 

Uroporphyrinogen I synthase 

Argininosuccinate lyase 

Adenylosuccinate lyase 

Cystathionine Y-lyase 

Cystathionine B-lyase 

Adenylate-cyclase 

Ribulosephosphate 3-epimerase 

UDP-glucose 4-epimerase 

L-Ribulosephosphate 4-epimerase 

UDP-glucinonate epimerase 

UDP-acetylglucosamine 4-epimerase 

UDP-acetylglucosamine 2-epimerase 

Methylmalonyl-CoA racemase 

Maleylacetoacetate isomerase 

Retinal isomerase 

Triosephosphate isomerase 

Arabinose isomerase 

L-Arabinose isomerase 

Xylose isomerase 

Ribosephosphate isomerase 

Mannosephosphate isomerase 

Glucosephosphate isomerase 

D-Lyxose ketol-isomerase 

N-(5’ –Phospho-D-ribosylformimino)-5-amino-1-(5’ –phosphoribosyl)-4- 

imidazolecarboxamide isomerase 

Glucose isomerase 

Glucosaminephosphate isomerase (glutamine-forming) 

Isopentenyldiphosphate isomerase 

Muconolactone isomerase 

Phosphoglycerate phosphomutase 

Phosphoacetylglucosamine mutase 

Phosphomannomutase 

Methylasartate mutase 

Methylmalonyl-CoA mutase 

Chorismate mutase 

Lanosterol-cyclase 

310

Muconate cycloisomerase 

myo-Inositol-1-phosphate synthase 

Succinyl-CoA-synthase 

Asparagine synthetase 

Glutamine synthetase 

Asparagine synthetase 

NAD+synthetase 

Pantothenate synthetase 

Y-Glutamylcysteine synthetase 

Glutathione synthase 

Phosphopantothenoyl-cysteine synthetase 

Phosphoribosylaminoimidazole-succinocarboxamide synthase 

UDP-N-acetylmuramoylalilne synthetase 

UDP-N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysyl-D-alanyl-D-alanine 

synthetase 

Phosphoribosylaminoimidazole synthetase 

GMP synthetase 

CTP synthetase 

Adenylosuccinate synthase 

Argininosuccinate synthase 

5’-Phosphoribosylamine synthetase 

Phosphoribosylglycinamide synthetase 

NAD+synthetase (glutamine-hydrolysing) 

GMP synthetase (glutamine-hydrolysing) 

Phosphoribosylformylglycinamidine synthetase 

Carbomoyl phosphate synthetase 

Pyruvate carboxylase 

Acetyl-CoA carboxylase 



Methylcrotonoyl-CoA carboxylase 

See metabolic pathways below. 

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313

314

315

316

317

318

319

320

321

322

323

324

325

326

327

For more on Metabolic Pathways: 

http://www.sigmaaldrich.com/Area_of_Interest/Life_Science/Metabolom 

ics/Key_Resources/Metabolic_Pathways.html?cm_mmc_o=TBBTkwCjCF 

wfz_BkBFbglCjC55gCjCFwfz_Bkbg%205zftczYl 

http://www.expasy.ch/cgi-bin/show_thumbnails.pl 

http://www.gwu.edu/~mpb/ 

328

Dr. Recommends is dedicated to developing statistical data banks to 

prove the efficacy of homeopathy to standard medicine and the world. 

Many studies have been done by Dr. Nelson in developing experimental 

and clinical proof for the efficacy and safety of homeopathy. 

DISCLAIMER 

If conditions persist, and are not responding properly to the 

homeopathic program, we encourage the doctor to make other referrals 

so that the condition will not deteriorate. Allopathic medicine has some 

dramatic benefits that can help with different disease structure in their 

crisis stages. 

Many patients do not go to doctors until they are in a crisis stage. 

Homeopathy might be too slow in working. We usually suggest that the 

patient use the remedies for two to four weeks if the condition allows. If 

results are not attained, the doctor should make a referral for more 

dramatic therapies. These should be discussed with a bio-physician who 

has an appreciation for the rules of nature. 

Homeopathic remedies are designed to work as an adjunct and support 

to standard medical therapies. They are not meant as a replacement. If 

symptoms persist, consult a medical doctor. If pregnant or lactating 

consult your physician. 

329

Continuing Education Units 

______________________________________ 

When you, the reader, finish reading the booklet 

you are allowed to credit yourself 

with the same number of CEU’s 

that you spent in hours reading the book. 

jÅA ]A VâÇÇ|Çz{tÅ? \ATAVAgA rrrrrrrrrrrrr 

Wtàx VÉÅÑÄxàxw 

330

The Natural Repertory of Prof. William Nelson

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