‘Miasmatic Analysis’- Confused Learners, Confused ‘Masters’. Utter Confusion For All!

‎’Miasmatic analysis’ is the sum total of ‘confusions’ created in the minds of already ‘confused’ learners, by ‘teachers’ who are gravely ‘confused’ themselves. The final outcome is ‘Utter Confusion for All’!

Some homeopaths appear to be experts in ‘miasmatic analysis’. Once a case is presented to them, they cannot avoid ‘miasmatic analysis’ of patients, drug substances or diseases. Instead of discussing symptoms and similimum, they would go on talking about miasms. It is funny to note that each ‘miasmatic expert’ would say there is no confusions if you understand it correctly. Then he would give his theories and ‘miasmatic analysis’. Then the next expert comes, and gives his theory and analysis, diametrically opposite to the earlier. He also says there is no confusions if you understand him correctly. I have never seen two ‘miasmatic experts’ talking about miasms in similar language. You give them a case for ‘miasmatic analysis’. Each would come with different analysis. AND YOU SAY, THERE IS NO CONFUSIONS!

I never seen two homeopaths explaining ‘miasms’ in same way. I never seen two homeopaths agreeing up on ‘miasmatic analysis’ of same case, same symptom or same medicine. Everybody talk differently. Is it does not indicate confusions? If you have any doubt on what I said, kindly post a case for ‘miasmatic analysis’ here. They would fight each other with their analysis. They would discuss strange concepts such as “psora merging into tuberculous spectrum”, or “psora converting into sycosis and then to syphilis as disease advances”. They would talk about ‘tri-miasmatic’ drugs, patients and diseases. I have seen it many times on this group. After all these intellectual exercises done, if you want to cure the patient, you have to find a similimum using symptoms! The simple truth is that appropriate similimum would cure even without any ‘miasmatic exercise’, if it is rightly selected.

One expert said: All individuals have all miasms, all drugs have all miasms, and all drugs have all miasms”, One would say warts are sycotic, another say it is psoric. A clever one would say warts have all miasms! Then why should we worry about miasmatic analysis?

I never said that the understanding of underlying miasms has no role in homeopathic therapeutics. Miasms, or ‘Chronic disease dispositions’ caused by infectious agents’ have to be considered and antidoted with appropriate antimiasmatic drugss. But, the intellectual exercises happening in the name of ‘miasmatic analysis’ is making everything a mockery, and UTTER CONFUSION FOR ALL.

In my opinion, the confusion would end only when we reach a consensus on ‘what is miasms’. If you could agree with my explanation of ‘miasms’ as ‘chronic disease dispositions’ caused by ‘off-target’ molecular inhibitions created by ‘antibodies’ generated in the organism against ‘exogenous’ protiens such as ‘infectious agents’, all confusions regarding ‘miasmatic analysis’ would be scientifically resolved. Until that happens, this confusion will remain.

Every chronic disease that is caused by ‘off-target’ molecular inhibitions created by ‘antibodies’ can be called ‘miasmatic diseases.

Let us consider a case of valvular heart disease caused by rheumatic fever. It was the antibodies formed against streptococcus sore throat infection that caused aarthritis, endocarditis, and valvular deformities. This chronic condition was caused by ‘off-target’ molecular inhibitions created by ‘antibodies’. It is a ‘miasmatic’ disease according to me. Same way, we know about chronic fibromyalgia caused by ‘chikunguniya’ antibodies, nephropathy caused by scabies antibodies, many chronic diseases caused by vaccinations. We can give a lot of examples

If we deeply study immunology and immune related diseases, we can understand the real scope of concepts I am trying to explain. A miasmatic disease one that is CAUSED by ‘Antibodies’ existing in the body, which were created earlier against ‘exogenous’ proteins that invaded the organism.

For example, a streptococcus sore throat is only an ‘infection’, not a MIASMATIC DISEASE. But, the artthritis and endocarditis caused by the antibodies generated by that infection are ‘miasmatic diseases’. Am I clear, sir? That is why hahnemann said ‘miasm’ is a ‘chronic disease disposition’ caused by ‘infectious agents’. He did not say ‘miasms are infectious diseases’. Please note the real difference.

Starting from pre-natal life, different kinds of antibodies are generated in our body against diverse types of ‘exogenous’ proteins including infectious agents. Actually, these antibodies are protein molecules of globulin types, which get deformed by getting acted up on by antigens. The active groups of antigens(epitopes) imprints upon the active groups of globulins(peritopes), in such a way that the peritope of globulin is converted into a ‘lock’ exactly fitting to the ‘epitope’ of antigen, which is similar to the ‘key’. Real ‘defense’ mechanism of organism is based on this ‘key-lock’ relationship. The problem arises when the ‘antibodies’ circulates in the body and bind to ‘off-target’ molecules, which have active groups with configuration mimicking the real antigen. This ‘offtarget’ bindings results in inhibitions of involved biological molecules, making them incapable of executing their natural functions. This is called a pathological molecular error, which expresses as a disease, and disease symptoms. This is the mechanism by which ‘antibodies’ or ‘miasms’ cause diseases.

I hope I have provided a most scientific, most logical explanation for the phenomenon of ‘miasms’. If you cannot understand or accept this concept, we are sure to differ in our approach to miasms and ‘miasmatic analysis’.

To discuss this topic, first you have to read my notes carefully, without prejudice, with a willingness to understand. Then, you have to understand it, for which you will have to update your biochemistry. Then you have to think over what I said. Then only we can have a meaningful discussions. If you have no time to read and understand what I say, there is no meaning in ‘discussing’. Please approach this concept without prejudice, because this is something different from what we have already learned.

We always think about ‘antibodies’ as ‘defense molecules’. Same time we should realize that they can act as pathogenic agents through OFF-TARGET interactions. Please learn more about hundreds of ‘auto-immune’ diseases to understand the real gravity of havoc these ‘immune’ bodies can create in the organism.

The problem is, our modern ‘miasmatic analysis experts’ have made us think all diseases in terms of ‘miasms’. The moment we mention a disease or symptom, or name of a drug, they start talking about ‘prominent miasm’, ‘tubercular spetrum’, ‘polymiasmatic’ and such phrases. The most funny thing is that ‘analysis’ of two experts never agree. They are confused, and make others confused. When talking about ‘miasms’ hahnemann was concerned only about ‘chronic disease dispositions’ caused by ‘infectious agent’. He asked to consider the presence of chronic ‘infectious miasms’ in cases where the diseases are not belonging to nutritional, environmental, occupational, iatrogenic and such causes. He used the term ‘faulty living’ and ‘faulty drugging’, which contain all these. In his perod, he knew nothing about ‘genetic causes’, and he did not mention those group of chronic diseases. Since he expressly said about miasms as ‘chronic disease dispositions’ caused by ‘infectious agents’, we can include ‘genetic diseases’ also in ‘non-miasmatic’ category. In fact, all chronic diseases, which are not mediated by ‘off-target’ molecular inhibitions caused by ‘anti-bodies’ formed in the body against ‘exogenous’ proteins, belong to ‘non-miasmatic’ category.

Listen, what I said: ” Miasms are chronic disease dispositions caused by off-target molecular inhibitions created by antibodies, which were generated against ‘exogenous’ proteing molecules including ‘infectious agents”. How can you interpret it in such a way that I said “all miasmatic disorders are autoimmune”? “Genetic disorders’ and ‘genetic expression disorders’ are different. Genetic disorders, which are due to actual errors in genetic substance or DNA, are beyond miasms. But, ‘genetic expression’ disorders or ‘protein synthesis disorders’ may be caused by influences of miasms, infections and many other exogenous or endogenous pathogenic factors, by acting up on the enzyme systems involved. That is the way pathogenic agents act.

I am trying to find out truth, not to satisfy somebody. I hope everybody would ultimately be satisfied with truth I am trying to find out truth, not to satisfy somebody. I hope everybody would ultimately be satisfied with truth

I never say “hahnemanns perceptions were wrong”. But, I would say many of his explanations regarding what he ‘percieved’ were imperfect, due to the infantile stage of scientific knowledge available to him in that time-space context he lived and worked. But many of the interpretations given by later ‘masters’ were wrong, and many times contrary to the real sense of hahnemann’s teachings. Miasms belong to that group. Hahnemann only said about a chronic diasease disposition caused by ‘infectious agents’. It was his interpreters, who mixed up miasms, genetics, embriyology and many other things, and created all these confusions. If uou studyy ‘miasms’ from original works of hahnemann, without the help of interpreters, you would be convinced of the truth in what I am saying.

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 undergo 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.

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 have many experiences with diseases caused by ‘off-target’ actions of antibodies. Streptococcus antibodies causing endocarditis and arthritis is an example. Sacbies antibodies causing nephropathy, chikungunia antibodies causing fibromyalgia, etc are commonly encountered. Long term side effects of various vaccinations also belong to this group. We know about various diseases appearing in mothers caused by antibodies formed against foetal proteins. Post-delivery psychiatric problems are associated with antibodies formed against some uterine infections and metritis. If you go through your immunology lessons, you will get hundreds of examples. Remember, this area of pathology is not so far well studied.
We have to study all the diseases included in ‘psora’ by hahnemann in this point of view. We have to expose the relationship between these diseases and infectious diseases considerd to be causative factors of psoric miasm.

So far, we have been studying about antibodies as ‘defense’ molecules only. We have to study them as ‘pathogenic’ agents also, especially playing behind many chronic diseases. New generation of homeopathy students can take up such studies as part of their academic research projects. I hope this discussions we do here may induce such creative thoughts in many minds

 

 

 

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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