Understanding ‘Miasms’ As ‘Antibodies’- Its Implications In Homeopathic Practice

During discussions on my scientific concept of ‘miasms’, many friends raised this question: “What difference it would make in practice, if we understand ‘miasms’ as ‘antibodies’?

I think this question is very much relevant, and I am bound to respond it positively.

First, we have to understand the exact molecular mechanism of  ‘pathology’ and ‘therapeutics’ in terms of modern biochemistry and molecular biology.

Antibodies are native globulin proteins ‘imprinted’ with exogenous protein molecules entering into the organism from the environment, as infections, food, drugs, toxins or as part of any interactions with the environment. These exogenous proteins may come from bacterial/viral/fungal/parasitic infections that invade the body, bites and stings of insects and serpents, uncooked food articles, drugs like antibiotics and serum, vaccines, and so on. These exogenous foreign proteins, alien to our genetic constitution, are dangerous to the normal functioning of the organism, and have to be destroyed or eradicated. Body has a well organized defense system for this, which we call immune system. Foreign proteins are called antigens. Body prepares immune bodies or antibodies against these dangerous invaders. Antibodies are specific to each antigen, There are also polyclonal antibodies, which can identify different antigens. Antibodies are exactly native proteins of globulin types, which have peculiar molecular structure with an active group known as ‘paratope’ on its periphery. Active groups of antigen molecules are known as ‘epitopes’. Epitopes of antigens and paratopes of antibodies has a ‘key-lock’ relationship of configuration. They should fit exactly each other in order to happen an immune reaction. Paratopes of antibodies once interacted with epitopes of a particular antigen undergoes a process of ‘molecular imprinting’, by which the ‘memory’ of epitope is imprinted into the paratope of antibody. Even after the antigens are destroyed and eradicated by the immune system, these ‘molecular imprinted’ globulins, or antibodies exist and circulate in the organism, in most cases life long. This is the mechanism by which life long immunity is attained through certan infections and vaccinations. These antibodies, or ‘molecular imprinted proteins’ are very important part of our defense system, playing a vital role in protecting us against infections.

Same time, these ‘molecular imprinted proteins’ or antibodies plays a negative role also, which is what we call ‘miasms’. They can act as pathogenic factors. Whenever these antibodies happen to come in contact with a native biological molecule having a structural group of configuration similar to the ‘epitope’ of its natural antigen, its paratope binds to it and inhibits the biological molecules. This is a ‘molecular error’ amounting to a state of pathology. Diverse types of chronic diseases and dispositions are created by the antibodies in the organism. These pathological conditions caused by ‘off-target’ binding of antibodies or ‘molecular imprinted proteins’ are the real ‘miasms’ hahnemann described as the underlying factors of ‘chronic diseases’.

Obviously, identifying and removal of these ‘off-target’ molecular blocks or ‘miasms’ caused by antibodies or ‘molecular imprinted proteins’ is an important part in the treatment of chronic diseases. Observing and collecting the whole history of infections and intoxications that might have generated antibodies are important in the management of chronic diseases. History of skin infections, venereal infections, stings of poisonous creatures, vaccinations, serum/antibiotic treatments, sensitization with protein foods  etc. has to be collected in detail and appropriate ‘anti-miasmatics’ included in the treatment protocols of  chronic treatments.

Another important thing we have to remember is that we cannot permanently inactivate ‘antibodies’ using potentized nosodes or anti-miasmatic drugs. Our drugs may act in two ways. If the nosodes are prepared from antibodies themselves, they contain ‘molecular imprints of  epitopes of ‘exogenous toxins’ or antigens themselves. These ‘molecular imprints can compete with the paratopes of antibodies in binding to biological molecues, and prevent them from creating ‘off-target’ biological blocks. Since ‘molecular imprints’ cannot successfully compete with the epitopes of antigens in binding with the paratopes of antibodies, our potentized drugs never interferes with the normal immune mechanism of the body. They only prevents antibodies from binding to ‘off-target’ biological molecules, and thus act as ‘antimiasmatics’.

If we are preparing nosodes by potentizing antibodies themselves, our drugs contains ‘molecular imprints’ of paratopes of antibodies. These molecular imprints can bind to the paratopes, thereby preventing them from interacting with ‘off-target’ biological molecules. Same time, they also cannot interfere in the interaction between antibodies and their natural antigens, which have comparatively increased affinity. In any way, potentized nosodes or ‘antimiasmatics’ will not weaken the normal immunological mechanism of the organism.

Since we cannot eradicate or permanently inactivate antibodies or miasms with our potentized drugs, we have to administer antimiasmatic drugs in frequent intervals, probably life long. This is a very important realization evolving from the understanding of ‘miasms’ as ‘antibodies’ or ‘molecular imprinted proteins’.

I think hahnemann included all ‘itch’ producing infections under the carpet of ‘psora’. He mentioned about Leprosy, scarlet fever, scabies and many such ‘infectious’ agents as causative factors of psora. He talked about “three miasms”, only because those three infectious agents were creating havoc in europe during his period. According to me, this classification of psora, syphilis and sycosis is not much relevant if we understand ‘miasms’ in terms of ‘antibodies’.

We should carefully study the whole history of patient to learn his ‘miasms’ or ‘antibodies’. For example, ‘vaccinations’. Each vaccination creates different types of miasms, which we have to antidote with appropriate nosodes . If the patient had history of severe allergy from bee stings, we have to antidote with apis. Same way, history of sanake bites, scabies, TB, everything will have to be considered.

Most of the bacterial toxins has a sulph containg ‘thio’ group on its epitome, and as such, potentized sulph would act as an antidote to almost all types of ‘antibodies’ or ‘miasms’ caused by such bacterial infections. That may be the reason why “sulph” became ‘king of anti-psorics’.

While considering ‘miasms’ of a patient, we should not limit ourselves to inquiries regarding history infectious diseases in his life. Antibodies may form against respiratory allergens such as pollens, fungus, housedust(contain mites), eggs, shell fishes, milk etc., all of which contains proteins exogenous to the body. History of anaphylaxis due to insect bites such as bees and wasps and snakebites should be noticed. History of vaccinations taken, including anti-rabies and anti-venom is also important. All such antibodies may act as chronic ‘miasms’ by attacking off-target biological molecules. We have lot of experiences with cases of kidney failures resulting from anti-rabies vaccinations. Many so-called auto-immune diseases are actually the chronic effects of ‘antibodies’ formed against exogenous proteins acting as ‘miasms’. Even though these ‘miasms’ may laso be part of ‘totality of symptoms’ during a perfect case taking, ‘miasmatic symptoms’ never come top during repertorizations. Hence, in the treatment of chronic diseases, ‘anti-miasmatic drugs’ and ‘nosodes’ should be considered, and applied in frequent intervals along with selected similimum.

NOW WE CAN SEE, THROUGH THE UNDERSTANDING OF ‘MIASMS’ AS ‘ANTIBODIES’, OUR MANAGEMENT OF CHRONIC DISEASES BECOMES MORE SIMPLE AND ACCURATE.

MORE OVER, OUR THEORY AND PRACTICE HAVE NOW BECOME MORE SCIENTIFIC, EXACTLY FITTING TO THE MODERN SCIENTIFIC KNOWLEDGE, ACCEPTABLE TO SCIENTIFIC COMMUNITY.

I THINK THIS IS A GREAT FORWARD STEP IN MAKING HOMEOPATHY A REAL SCIENTIFIC MEDICAL SYSTEM

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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