‘Miasms’- Understanding Its Biological Mechanism As Residual Effects Of Infectious Diseases
My work on ‘miasms’ started from two basic convictions:
Firstly, I am convinced that infectious diseases have life-long residual effects on our organism, producing chronic constitutional disease dispositions.
Secondly, I am convinced that any disposition, disease, sensation, mental condition, emotion or constitutional tendency will have a material, ‘molecular level’ biochemical basis underlying it, and a biological mechanism through which it is executed.
Begining with hahnemann’s observation that ‘miasms’ are chronic disease dispositions produced by infectious diseases, I wanted to know the molecular level material basis of miasms, and the biological mechanism by which they produce chronic diseases.
My inquiry was, how can an infectious disease produce ‘residual effects’ in the body even after the infection is over. What remains in the body that can produce such a residual effect?
One thing common to all infectious agents are that all of them introduce some chemical molecules of protein nature into the host, which act as antigens and lead to the production of ‘antibodies’ or immune substances that help the body to fight the invading infectious agents.
Antibodies are native globulin proteins imprinted with antigens, and can bind to the specific antigens by conformational affinity. These antibodies remain in the organism even after the infection is over.
It is these antibodies generated in the organism against specific infectious agents, that produce ‘residual effects’ which hahnemann called miasms. Antibodies circulate in the body, and can bind to various ‘off target’ bilogical molecules such as receptors and enzymes, producing molecular inhibitions in various biochemic pathways. They produce many chronic pathological conditions we call as ‘auto immune’ diseases. Antibodies can even bind to enzymes involved in biochemical processes of genetic expressions, producing phenotype changes in constitutions. It is these phenotype changes that underlie the dispositions we call ‘miasmatic constitutions’.
Any substance of PROTEIN nature, alien to the genetic code of a given living organism can act as MIASM when it enters into the system, by generating antibodies that can bind to ‘off-target’ biological molecules and produce pathological molecular inhibitions. Bacteria, virus, vaccines, body fluids of other animals, venoms, biological toxins, deformed proteins or any other substance of protein structure that do not agree with the genetic code of the host can act as miasms. Hahhnemann studied only ITCH, GONORRHOEA AND SYPHILIS, since those three infectious agents were most rampant in europe during his time, causing many chronic disease conditions in the population. Hahnemann never said miasms are ONLY three.
I have identified the material level molecular basis of ‘miasms’, and explained the biological mechanism by which they produce ‘chronic disease dispositions’. I think my work has contributed in the scientific advancement of hahnemann’s concept of miasms, thereby making it fitting to the modern scientific knowledge system. I have shown that masm is not an unscientific belief, but a scientific fact.
According hahnemann, MIASMS are not INFECTIOUS DISEASES as such- but miasms are CHRONIC DISEASE DISPOSITIONS produced by infectious diseases. Miasm is the chronic RESIDUAL effects of infectious diseases that remain IMPRINTED in the organism for the whole life, which produces disease dispositions, constitutional derangement, and obstructions to cure. Please note that point.
Modern ‘miasmatic experts’ ignore the fact that no where hahnemann talks about miasms unconnected with ‘infectious diseases’. If you read ‘chronic diseases’ carefully, you will realize that hahnemann considered miasms ONLY as ‘chronic disease dispositions’ produced by infectious diseases. He says very specifically that PSORA is the miasm of INFECTIOUS ITCH, SYPHILIS is the miasm of SYPHILIS INFECTION, and SYCOSIS is the miasm of FIGWARTS/GONORRHOEA infection.
It is the later ‘interpreters’ who disconnected miasms from infectious diseases, and started to explain miasms as ‘constitutional dispositions’, ‘genetic inheritence’, ‘original sin’, ‘mental make up’ ‘deviated vital force’ and such things, thereby creating all confusions now known as ‘miasmatic analysis’.
If you really want to study hahnemann’s concept of miasms, and to understand my scientific explanations for it, you should start by carefully reading ‘chronic diseases’. You will be gravely misguided if you try to learn miasms from the works of later interpreters known as ‘miasmatic experts’- they have hijacked hahnemann’s original idea to make it fit to the nonsense theories and methods they propagate. They are confusing the whole homeopathic community with their futile intellectual pretensions and obscurantism in the name of ‘miasmatic analysis’, masking their own ignorance and confusions by playing with complex phrases meaning of which even they fail to understand.
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