‘Keynote Symptoms’ and ‘Keynote Prescriptions’- An Analysis From MIT Perspective

A KEYNOTE symptom is a specific ‘symptom complex’ of ‘accessory symptoms’ that when appears associated with an ABNORMAL BASIC SYMPTOM in a patient, specifically indicates a particular remedy. These KEYNOTE ‘symptom complexes’ are constituted by two or more very characteristic ‘accessory symptoms’ belonging to categories such as causations, locations, presentations, sensations, modalities and concomitants.

A Keynote ‘symptom complex’ becomes more useful in practice, when it contains minimum number of ‘accessory symptoms’ and it indicates minimum number of drugs- preferably SINGLE drug. In such cases, that drug could be prescribed very easily, and with full confidence.

Keynote symptom is a symptom, which if present in a patient, will directly lead us to a specific remedy. That symptom will work as a KEYNOTE in deciding a prescription for that case.

Most probably, a ‘keynote’ symptom is a ‘symptom complex’ that represents a specific molecular error produced in the organism by a specific pathogenic molecule. When same ‘keynote’ ‘symptom complex’ is also present in a drug, that shows the drug also contains a constituent molecule similar to that pathogenic molecule, which produced similar molecular errors during drug proving. Due to that similarity, molecular imprints of that particular drug molecules can bind specifically to those pathogenic molecules, there by removing the molecular inhibitions they produced in biological molecules.

‘Totality of symptoms’ in a patient means totality of all the diverse types of ‘symptom complexes’ expressed by the patient, representing all the diverse types of molecular errors produced by all the diverse types of pathogenic molecules.

‘Keynote symptom’ in a patient means a particular ‘symptom complex’ expressed by the patient, representing a particular type of molecular error produced by a particular type of pathogenic molecule.

When finding similimum by ‘totality of symptoms’, we are trying to find a drug that contains maximum number of diverse chemical molecules matching to maximum number of diverse pathogenic molecules that produced the diverse types of molecular errors as well as ‘symptom complexes’ in that particular patient.

When finding similimum by KEYNOTE method, we are trying to find a particular drug that contains a particular constituent molecule that is SIMILAR to a particular pathogenic molecule that produced a particular molecular in the organism and expressed through a particular ‘symptom complex’.

KEYNOTE PRESCRIPTION tries to address a case by identifying a specific molecular error in the patient, where as TOTALITY OF SYMPTOMS tries to address the case by considering maximum number of diverse molecular errors existing in the patient.

In KEYNOTE prescriptions, we select a similimum by considering only specific SYMPTOM COMPLEX representing a specific MOLECULAR ERROR in the patient as a standard single UNIT, and identifying a drug that could produce SYMPTOM COMPLEX similar to it during drug proving.

‘Burning pains in stomach, amel by cold drinks’ is a KEYNOTE of APIS MEL. Here, this keynote ‘symptom complex’ consist of ‘burning- sensation’, ‘stomach- location’, and ‘amel by cold drinks- modalities’.

‘Urticarial skin rashes alternating with asthma’ is a KEYNOTE of CALADIUM. Here, the keynote symptom complex consist of ‘urticaria- presentation’, ‘skin-locations’ and ‘alternating with asthma- concomitants’.

‘Fever with Urticaria after getting wet in rain’ is a KEYNOTE of RHUS TOX I have compiled. This ‘symptom complex’ is constituted by ‘fever-presentation’, ‘getting wet in rain- causation’ and ‘urticaria during fever- concomitant’. This is an example of preparing KEYNOTE symptom complexes by combining ‘accessory symptoms’. We can confidently prescribe RHUS TOX in any case of ‘Fever with Urticaria after getting wet in rain’ on the basis of this KEYNOTE.

‘Cramping pain abdomen after eating, amel by pressure’ is a KEYNOTE of COLOC. This symptom complex is constituted by ‘abdomen- location’, ‘cramping pain- sensation’, ‘eating- causation’ and ‘pressure- modality’. COLOCYNTHIS is a sure-shot remedy for this type of abdominal pains.

‘Fatty degeneration of liver with desire for warm food’ is a KEY NOTE of CHEL and LYCO. If the patient is HOT, it is LYCO. If he is cold, it is CHEL. This is another example of selecting similimum by using KEYNOTES.

You can analyze any known keynote symptoms in this way. That will help you in synthesizing a lot of new keynote symptom complexes by combining small characteristic rubrics from repertories, so as to indicate single specific drugs. That will make your clinical practice very easy, by compiling a complete collection of strong KEYNOTES that could be combined with any basic symptoms appearing in your patients.

KEYNOTE SYMPTOMS are interpreted as ‘main theme of medicine’ by ‘classical homeopaths’. According to them, a drug will have only a single keynote. They say keynote of fluoric acid is ‘destructiveness’, keynote of carbo-veg is ‘imperfect oxidation and disintegration’, key note of aethusa is ‘violence’.

According to their view, a keynote will be a mental or general only, and there will be only one main theme or keynote for a drug. They should explain, if ‘destructiveness’ is the keynote or main theme- of acid fluor, it is useful only in cases having ‘destructiveness’? What about other drugs having ‘destructiveness’? How can anybody select acid fluor only on the basis of ‘destructiveness’, ruling out other drugs having ‘destructiveness? What is their evaluation of the great work of H C ALLEN onn keynotes of different drugs? Did he list only ‘destructiveness’ under acid fluor?

Please see allen’s keynotes. Nowhere he mentions ‘destructiveness’ as keynote under acid fluor. He has given following keynote symptoms for acid fluor. He never mentions them as ‘main themes’.

“Complaints of old age, or of premature old age; in syphilitic mercurial dyscrasia; young people look old.

Increased ability to exercise without danger (Coca.); is less affected by excessive heat of summer or cold of winter.

Old cicatrices become red around edges, and threaten to become open ulcers (Caust., Graph.).

Varicose veins and ulcers, obstinate, long standing cases, in women who have borne many children.

Caries and necrosis, especially of long bones, psoric or syphilitic, abuse of mercury or silica (Angus.).

Naevus, flat, of children (r. temple); capillary aneurism (compare, Cal. fl., Tub.).

Ulcers: red edges and vesicles; decubitus; copious discharge; < from warmth, > from cold; violent pains, like streaks of lightning, confined to a small spot.

Rapid caries of teeth; fistula dentalis or lachrymalis; exostosis of bone so face (Hekla).”


Actually, a KEYNOTE symptom is a symptom, which if present in a patient, will directly lead us to a specific remedy. That symptom will work as a KEYNOTE in deciding a prescription for that case.

Author: Chandran Nambiar K C

I started practicing homeopathy in 1970, when I was 20 years old and studying for final year of BSc (Zoology) course. My interest in homeopathy happened very accidentally, through a constant relationship with a local practitioner who happened to be father of my classmate. I was a regular visitor in his clinic, where from I started reading BOERICKE MATERIA MEDICA and other homeopathic books, which helped me to cure myself my troublesome asthma that have been haunting me since my childhood days. I became a voracious reader of homeopathy. I was also deeply involved in studying marxism and dialectical materialism during my college days, which attracted me to political activities. MARXISM and HOMEOPATHY became two essential parts of my intellectual and practical life, which still continues so. Even though I joined DHMS course in a karnataka homeopathic college, I could not continue it due to my intense involvement in revolutionary political activities that resulted in jail life and a lot of criminal cases. Once that phase was over, I took a diploma in veterinary science and became a livestock inspector in animal husbandry department under govt of kerala. I have been continuing my study and practice of homeopathy all through these years. Since CCH act came into force only in 1976, and it contained provisions allowing existing practitioners to continue, my homeopathic practice went smoothly in parallel with my government job. In 1987, co-operating with some local homeopaths and social activists, I started Kannur District Homeopathic Hospital Sociey, which established a chain of hospitals and homeopathic clinics in different parts of Kannur district. After a few years I had to leave the society for some political reasons, and I established a 100 bedded well equipped homeopathic hospital in Taliparamba, employing a number of prominent homeopaths. That was ended up as a financial disaster for me due to many reasons, including my lack of skills as a money manager, and I was compelled to close down my dream project with in a short period. I lost huge money I invested, lost my reputation, and it pulled me into a debt trap. I learned a lot of valuabl lessons from this failure- about life, human psychology, relationships, and above all, about myself. I realized failure is the greatest teacher, if you are prepared learn from it. I learned how will power and determination to win will help us come back into life as a phoenix from our own ashes. I learned, one does not fail unless he stops fighting and accepts failure. My failure and the hardships that followed has moulded my personality in such a way that I can now withstand any disaster and fight back. I tell you, you will not know what life really is, unless you miserably fail at least once in your life. By this time, I left my government job also, and settled as a full time homeopathic practitioner. By this practice, I could repair my earlier financial losses, and establish well in life. It was during this period that I felt the need of developing a simple and user-friendly homeopathic software, that resulted in the evolution of SIMILIMUM, which was later upgraded into SIMILIMUM ULTRA. Similimum Ultra was well accepted by the profession, and it collected good revenues which continues even today. I stopped my practice a few years back , and concentrated in the study and research activities to evolve scientifically viable explanations to the so-called riddles of homeopathy. This unrelenting study resulted in MIT or Molecular Imprints Therapeutics, which provides a scientific and rational explanation for homeopathy. I started a homeopathic discussion group on facebook called HOMEOPATHY FOR TOTAL CURE, which has more than 35000 homeopaths as members. By this work on facebook, I could establish close relationship with many homeopaths around the world. It goes on. I could successfully convert facebook as my office and work place, from where I propagate my MIT ideas, co-ordinate my works for homeopathic community, and sell my Similimum Ultra Software. My years of hardwork in search of HOW HOMEOPATHY WORKS ultimately resulted in the publication of a book titled REDEFINING HOMEOPATHY (3000 pages, 3 volumes, hard bound, Rs 6000), in which I have compiled my articles regarding my scientific explanations of basic principles of homeopathy. These ideas are called MIT or MOLECULAR IMPRINTS THERAPEUTICS. MIT is now included in the syllabus of MD (HOM) course of prestigious DY PATIL DEEMED UNIVERSITY, PUNE, INDIA. Research department of SARADA KRISHNA HOMEOPATHIC COLLEGE, Kulashekharam, Tamilnadu, India, the only NAC accredited homeopathy college in India, has recently taken up certain reserch projects for proving the scientific explanations proposed by MIT. Based on MIT perspective of homeopathy, I had developed an MIT PROTOCOL for scientific homeopathy, and initiated a project for establishing a chain of MIT NETWORK CLINICS all over India, where MIT PROTOCOL will be practiced. More over, I have developed a whole range of 351 MIT FORMULATIONS, which are disease-specific combinations of post-avogadro diluted homeopathy drugs. NOW I AM IN 71st YEAR OF MY LIFE, AND STILL LOOKING FOR NEW HORRIZONS!

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