How The Concept Of MIT Influences The Way Of Combating Miasms In Chronic Diseases?

Classical concepts of ‘miasms’ and methods of ‘miasmatic analysis’ for selecting ‘anti-miasmatic’ drugs will undergo drastic changes when we accept the definition of homeopathy as ‘Molecular Imprints Therapeutics’. According to new approach, hahnemann’s concept of miasms is redefined as chronic disease dispositions due to ‘off-target’ molecular inhibitions caused by antibodies formed against ‘alien’ proteins including infectious agents entering the organism. Most of these antibodies exist life-long inside the organism, causing diverse types of chronic diseases which include so-called auto-immune diseases also. To combat these chronic effects of anti-bodies, specific nosodes and other ‘anti-miasmatic’ remedies containing ‘molecular imprints’ that could de-activate these antibodies will have to be used. Anti-miasmatic ‘molecular imprints’ will have to be selected on the basis of infectious diseases, vaccinations and anaphylactic histories. Properly selected specific anti-miasmatic drugs will have to be used along with symptomatically selected drugs, especially in ‘total cure’ prescriptions.

Theoretically, ‘totality of symptoms’ include symptoms of ‘miasms’ also. I think ‘symptoms’ need not be the ‘only’ factor to considered if we have an exact understanding of ‘molecular level pathology’. Symptoms are only ‘one of the tools’ for identifying pathological molecular errors and selecting remedial agents’. When we know the ‘causative’ factors. we can prescribe without considering symptoms. Locating the ‘molecular errors’ is the primary concern, whatever be the tools we utilize for that.Theoretically, ‘totality of symptoms’ include symptoms of ‘miasms’ also. I think ‘symptoms’ need not be the ‘only’ factor to considered if we have an exact understanding of ‘molecular level pathology’. Symptoms are only ‘one of the tools’ for identifying pathological molecular errors and selecting remedial agents’. When we know the ‘causative’ factors. we can prescribe without considering symptoms. Locating the ‘molecular errors’ is the primary concern, whatever be the tools we utilize for that.

Materia medica of nosodes are much imperfect, and repertories do not represent them in due importance. Due to this limitation, we never get nosodes as similimum through symptomatic repertorization.

Not only past ‘illness’, we should also consider history of vaccinations and ‘allergies’, when we define miasms as antibodies against ‘alien proteins’.

So called ‘allergies’ have to be considered from miasmatic point of view. Allergic sensitizations happen due to the interaction of immune system with ‘allergens’ which are in most cases alien proteins. Potentized allergens would contain molecular imprints of these alien proteins, and hence should be considered as nosodes.

Allergy is actually the reaction of organism towards an ‘alien’ protein entering the organism. Antibodies are formed as a mechanism for trapping, marking and destructing these alien proteins, which are harmful to the system as they are proteins that do not match to the ‘genetic blueprint’ of the organism. As such, we can say, allergy is the reaction of organism towards proteins that do not match to its own genetic blueprint. That is why they become ‘aliens’. Even ‘egg albumin’, ‘saliva’ or ‘serum’ of an animal belonging to another species become deadly poisons due to the mismatch of genetic blueprint and protein molecules.

You can see, the MIT approach makes the concept of ‘miasms’ much broader than classical approach. Instead of three miasms originating from three major infectious diseases that was widely prevalent during hahnemann’s time, now we can see all ‘chronic disease’ dispositions originating from antibodies formed against diverse types of ‘alien’ proteins. This approach help us to perceive so-called ‘auto-immune’ diseases from a new angle. It is known that many ‘auto-immune’ diseases such as psoriasis, vitiligo and chrohn’s disease actually begins after some infections or allergic sensitizations, which shows the currently accepted ‘auto immunity’ theory will have to be re examined. In my opinion, so-called ‘auto-immune’ diseases are also caused by off-target molecular inhibitions created by antibodies formed against alien proteins. In other words, auto-immune diseases are also ‘mismatic’ in origin, and can be treated with appropriate nosodes.

Obviously, re-evaluation of the concept of ‘auto-immune diseases’ in modern medical science is a very important implication of MIT definition of homeopathy.

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!

One thought on “How The Concept Of MIT Influences The Way Of Combating Miasms In Chronic Diseases?”

  1. Concept of ‘miasm’ was brought in by Hahnemann ,when he was not able to cure the patients from diseases with a set of subjective/objective symptoms,using the homeo-pathic theory. I am of the opinion that concept is there because of the limitation of finding appropriate similimum for the given patient with the symptoms vs remedies. Author, here, again confused himself by saying ‘antibodies’,’vaccinations’ etc. Molecular imprint theory explains every phenomena of causing disease in living systems,without bringing in antibodies ,vaccinations etc,if it is believed that any ‘alien’agents cause molecular defect in living system causing diseases.
    I feel that the concept of ‘miasm’can be managed by collecting a set of symptoms V/S remedies ,and re-arranging repertory,thus enabling finding appropriate similimum for the set of subjective /objective symptoms.
    In fact no repertory is complete and perfect per se.Every repertory is found different, in some cases,with differently graded remedies.That shows that remedy proving is to be calibrated to get a real ‘standardized repertory’.
    In fact vaccination,infection etc contribute to their characteristic ‘molecualr defects’in the patient,as is the case with toxin or pollutants ingestion or from hereditary factors.
    If MI theory is taken ,antibodies are to be taken as the ‘defect’ .

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