STILLS'S DISEASE AND HOMOEOPATHY

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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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THE NEED OF DETAILS AND GENERAL CHARACTERISTICS IN A HOMOEOPATHIC CASE.

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In today’s article I want to address a very common and frequent question which comes to the mind of students as well as patients. WHY DOES HOMOEOPATHY REQUIRE DETAILED INFORMATION IN TREATING A DISEASE? The most basic answer is due to its innate principle of holism. i.e viewing and treating   the man as a whole entity and not the disease alone. But still, the question remains the same. Well, in today’s world disease is viewed as a mere local phenomenon, which is caused due to some dysfunction in the body, leading to a specific group of symptoms. Though this seems true there is also something beyond and deeper than this superficial view. This belief on diseases is rather like a tip of the iceberg. We can see only the tip. However the actual body of the iceberg is invisible though, present. And we have also witnessed the tragedy that struck the mighty Titanic which was caused by ignoring the root though the tip was visible. The same is also true with diseases. The actu...
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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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