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 am Chandran Nambiar K C Author, REDEFINING HOMEOPATHY Managing Director, Fedarin Mialbs Private Limited Developer. SIMILIMUM ULTRA Homeopathic Software I am not a scientist, academician, scholar, professional homeopath or anybody with 'big credentials', but an old lay man, a retired government servant, who accidentally happened to fall into the deep waters of the great ocean of homeopathic knowledge during his fiery teenage years, and was destined to live a whole life exploring the mysteries of that wonderful world with unending enthusiasm. My interest in homeopathy happened very accidentally when I was only 20 years old UNDERGRADUATE ZOOLOGY student, 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.

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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