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    MIASMS- The Killer Bodyguards
    MIASMS- The Killer Bodyguards
    MIASMS- The Killer Bodyguards
    Ebook96 pages1 hour

    MIASMS- The Killer Bodyguards

    By Chandran K C

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    About this ebook

    Starting from 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'.

    LanguageEnglish
    PublisherChandran K C
    Release dateJun 13, 2018
    ISBN9780463734520
    MIASMS- The Killer Bodyguards
    Author

    Chandran K C

    Chandran K C Pioneering a Scientific Revolution in Homeopathy In late sixtees, a 20 year old zoology degree student already armed with the theoretical tools of dialectical methodology, accidently happened to fall into the great ocean of wonderful knowledge of homeopathy, started loving, questioning, learning, exploring, experimenting, and applying it in a way totally different from that of his predecessors. Later in his life, he even dared to quit his job in animal husbandry department under government of kerala, to dedicate his whole time and energy for homeopathy. ‘SIMILIMUM ULTRA HOMEOPATHIC SOFTWARE’ & the book, ‘REDEFINING HOMEOPATHY – as Molecular Imprints Therapeutics’ are the final outcomes of that life devoted for homeopathy for last forty eight years. He is 67 years now. He was the founder of the prestigious Kannur District Homeopathic Hospital Society, establishing a chain of hospitals and clinics for the promotion of homeopathy. Now, he is engaged in serious studies and research activities for proving his scientific explanations of homeopathy, which is expected to revolutionize not only homeopathy, but the whole medical science and pharmaceutical industry in the coming days Email: similimum@gmail.com Mobile: +91 9446 520 252 Address: KC House, Malappattam- 670631, Kannur, Kerala, India

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    Book preview

    MIASMS- The Killer Bodyguards - Chandran K C

    MIASMS

    Killer Bodyguards!

    By

    Chandran K C

    Copyright 2018 Chandran K C

    A Smashword Edition

    Chapter 1. Redefining 'Miasms'

    Homeopathic understanding and management of ‘chronic disease’ is based on the concept of ‘miasms’. Hahnemann has provided detailed explanations regarding three types of ‘miasms’ such as ‘psora’, ‘syphills’ and ‘sycosis’. Theory of  ‘miasms’ and chronic diseases were developed during later part of Hahnemann’s life, when he learned from his clinical experience that medicines selected on the basis of similarity of symptoms as he advocated earlier offered only temporary relief to the most patients.

    According to his theory of ‘chronic diseases’, ‘psora’, the ‘miasm’ of suppressed ‘itch’, is the underlying primary cause of all chronic diseases other than those of ‘venereal’ origin. ‘Psora’ is said to be the greatest obstruction to cure. Other two miasms, ‘syphilis’ and ‘sycosis’ are considered to be miasms of venereal diseases, ‘syphilis’ and ‘gonorrhoea’ respectively. Hahnemann considered ‘psora’ to be the most important and universal ‘miasm’. According to his theory, unless this ‘miasm’ or ‘disease poison’ is eradicated with appropriate ‘anti-psoric’ drugs, permanent and lasting cure cannot be attained.

    The primary forms of expression of ‘psora’ is considered to be the itching eruptions on skin, that of ‘syphilis’ un-healing tissue destructions like malignant ulcers, and that of ‘sycosis’ warts and condylomata.

    Symptoms of primary ‘psora’ include the different types of itches and eruptions that appear on the skin. Hahnemann considered the ‘miasm of psora’ to be inherited through generations of human kind.

    Now, let us try to analyze the concept of miasms and chronic diseases in the light of scientific understanding of molecular biology, ‘similia similibus curentur’ and ‘potentization’.

    Human organism is constantly exposed to the attacks of various types of exogenous and endogenous foreign molecules and ions. They may bind to the complex native biological molecules, thereby deforming their configuration and making them incapable of participating in the normal bio-chemical interactions. As per scientific view, this phenomenon underlies the molecular basis of most pathological conditions.

    If the pathological foreign molecules are of protein nature, native biological defense proteins having configurational affinity to these foreign proteins attaches to them, destroys and removes them from the organism as part of body’s defense mechanism.  During this defense process, some of the involved native protein molecules get configurationally deformed by the interaction with foreign molecules. Native protein molecules so deformed will be carrying the 3-D spacial impressions of the interacted foreign molecules on their periphery. These impressions exist as three dimensional pockets, having a configuration complementary to that of foreign proteins. These molecular imprinted proteins thus become incapacitated for their normal biological processes, and remain a burden in the organism. Antibodies actually belong to this class of such deformed globulin proteins, subjected to ‘molecular imprinting’ by foreign proteins.

    Certain endogenic molecules and ions such as hormones, neuro-chemicals, and other metabolic byproducts such as super-oxides, when circulated in excess, may   also attach to various bio-molecules other than their natural targets, and induce configurational changes in them.

    These deformed native proteins may circulate in the system, and accidentally attach to various bio-molecules having complementary configurational affinity, thereby creating various molecular errors and pathological deviations.

    Configurational changes happening in enzymes of protein nature involved with genetic expressions and DNA synthesis may ultimately lead to various types of proteinopathies, or may result in mutations happening in genetic substance itself, with subsequent hereditary diseases. If the enzymes involved in genetic expressions get deformed by molecular imprinting, it may affect the process of normal protein synthesis, and produce related pathological conditions. It may be noted that heavy metal ions and certain poisonous substances such as alkaloids and organophos chemicals also can inhibit the enzymes associated with DNA synthesis, and create genetic errors.

    Obviously, modern scientific knowledge regarding subjects such as antibodies, proteinopathies, genetic expressions, molecular imprinted proteins, etc., were not available during the era of Hahnemann, when he undertook the study of chronic diseases. Had he understood the exact bio--molecular basis of these phenomena, he would have provided a theory of chronic diseases entirely different from that he had formulated.  At that time, it was the wonderful insight of the  great genius of Hahnemann that enabled him to observe the deep-seated factors playing behind the  chronic diseases that he called ‘miasms’. During that period, even before the appearance of antibiotics modern microscope, most dreaded diseases such as eczema, leprosy, syphilis and gonorrhoea were rampant in europe. He observed that in spite of the various crude forms of treatments available then, these diseases continued their manifestations during the whole life span of patients. Naturally, his theory of chronic disease was more involved with the long term effects of these diseases. He used the term ‘miasm’ to describe these chronic disease factors. By the term ‘miasm’, he really meant ‘disease poisons’. The miasm of ‘itch’ (and leprosy) was called as ‘psora’, the ‘miasm of syphilis as ‘syphilis’, and that of gonorrhoea as ‘sycosis’. Now, based on modern scientific knowledge, we can say that ‘miasms’ are the antibodies or ‘molecular imprinted proteins’ created in the organism due to the interaction of native proteins with various bacterial, viral or fungal toxins of protein nature. Various environmental allergens, and certain endogenous molecules and metabolic bye-products may also imprint up on native defense proteins and convert them into chronic ‘miasms’.

    Antibodies produced in the organism against scabies (itch), leprosy, and tuberculosis belong to same class, and give positive reaction to ‘tuberculin’ antigen tests. This indicates that toxins released by these bacteria have certain similar molecular groups in them, and the molecular imprints or antibodies against those groups also have certain configurational similarities. Actually, these ‘molecular imprints’ belong to the ‘miasms’ of ‘psora’ described by Hahnemann. Homeopaths already know that potentized ‘tuberculinum’, ‘bacillinum’, and ‘psorinum’ play a wonderful role in the treatment of scabies and other skin eruptions, and the chronic conditions related with them.

    It may be interesting to observe that toxins released by bacteria belonging to mycobacterium group, are molecules containing ‘sulphur’ in their active groups. The presence of sulphur-containing amino acid called cysteine is responsible for this factor. During infection, bacterial toxins bind to the biological molecules of organism using this sulphide group. Naturally, ‘molecular imprints’ or

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