India, which shares 17% of global population, has finally had its first dedicated policy on making treatment of rare diseases accessible and affordable. by Dr. Dipanjana Datta While rare diseases are...
When his daughter, Meredith Huml, was diagnosed — finally — with facioscapulohumeral (FSHD) muscular dystrophy in 2004, Raymond Huml immediately jumped into action, researching everything he could about the disease and reaching...
आज लोक सभा में लाईलाज बीमारी मस्कुलर एट्रोफी व डिस्ट्राफी से झुंझ रहे बीमार बच्चो व वयस्को की समस्या व उनके इलाज की मांग को लेकर मामला उठाया,स्पाइन मस्कुलर एट्रोफी...
https://youtu.be/VOCwHi0p9OM Link For The Original Video:-...
GUWAHATI: A complicated and rare bicuspid aortic valve surgery on a 41-year old woman of the state was successfully carried out recently at GNRC Hospitals here, which is the first...
Inborn error of metabolism (IEM) is a spectrum of diseases that can affect the normal metabolism in children, said doctors. Screening of newborns or screening of parents during the pre-natal...
The High Court of Karnataka on Friday passed an interim order to shift a toddler afflicted with Spinal Muscular Atrophy (SMA) Type 1, a rare disease, to the Indira Gandhi...
In an exclusive interaction with BW Health care world, Subhamoy Dastidar, Co-Founder & Director, Lilac Insights, speaks about the firm and more. Excerpts: Tell us about the recent trends in...
Aimed at raising money for treatment of rare diseases that need expensive and life-long treatment and affect a small percentage of the population News:- 1)Platform launched on August...
