STILLS'S DISEASE AND HOMOEOPATHY

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MIASMS IN HOMOEOPATHY

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MIASMS IN HOMOEOPATHY INTRODUCTION Miasms   in homoeopathy are considered as the most vital part in understanding diseases as well as a vital key to a successful prescription. These are considered as the most fundamental aspects of a diseases specially of a chronic character   as they represent a manifestation of an internal derangement. SO WHAT DO THEY MEAN In simple sense they are a predisposition to a particular disease inherited or acquire. THE THEORY IN ACTUAL According to the theory of miasms it is said that behind a given case of disease specially of a chronic character their lies a particular cause which dries the disease to expand itself beyond the body innate efficient immune response and resisting it thereby rendering it to continue actively life long and giving it a chronic character. It also represent they way of body’s response to a given state of disease. Which is manifested   in three basic ways. 1.       ...
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MUSCULAR DYSTROPHY: A RARE GENETIC AILMENT AND ITS MANAGEMENT IN HOMOEOPATHY.

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MUSCULAR DYSTROPHY: A RARE GENETIC AILMENT AND ITS MANAGEMENT IN HOMOEOPATHY.   11 December 2023. Talking about certain crippling ailments, haunting and daunting humanity from the longest of time, and even continuing to  wreak its havoc even today, and frankly medical science not able to find a way out of it till date. So one may ask that whether or not will we ever able to conquer it or not anytime? Well, at present I, in my knowledge and experience cannot say when and how but the only way out is to be positive .One such rare ailment in todays talk is MUSCULAR DYSTROPHY. SO, WHAT IS MUSCULAR DYSTROPHY? Muscular Dystrophy is group of rare genetic disorders, which chiefly affects the muscles making them weaker over-time and consecutively weakening and wasting away muscle strength, stability and control, to such an extent that the person is not able to lift himself up after sitting a the chair. AND HOW DOES THAT HAPPEN?             W...
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PRIMARY CILIARY DYSKINESIA AND KARTEGENER'S SYNDROME

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PCD/PRIMARY CILIARY DYSKINESIA AND KARTEGENER’S SYNDROME.                 PCD/Kartegener’s syndrome is a rare genetic disorder, which is characterized by defects or complete loss of ciliary action which is covering the entire respiratory tract thereby causing defective mucosal clearance.                 Cilia are small hair like structures, which are located in the respiratory tract(upper and lower), sinuses, Eustachian tube of the ear, miaddle ear and flagellas of sperms. These cilia function as a protective structures, trapping invading particles, to enter the respirtatory tract. Moreover, their chief function is swaying movement, which generate currents thereby helping in transport or expulsion of mucous towards the throat in case or respiratory tract and ear. In case of sperm cells and fallopian tube, they help in t...
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