The child’s father approached the Court seeking free treatment from the State. One dose of the required life-saving drug costs Rs. 18 crores. The Kerala High Court on Tuesday directed...
The IGICH will face a serious difficulty from August 2021, the High Court observed on June 18 this year. BENGALURU: In an ongoing case in the Karnataka High Court...
World Vitiligo Day aims to raise awareness on #Vitiligo, a rare condition. Join us in breaking barriers and embracing the vitiligo warriors. #WVD2021. We appreciate the kind assistance of Ms....
We appreciate the kind assistance of Ms. Sailakshmi Iyer, Ms. Anandi Shivaram, and Ms. Dhanushya, MSc BMG, VIT, Vellore for the poster on Dravet Syndrome Awareness. Visit This...
Reports of rare clotting and bleeding disorders in younger adults, some fatal, led a number of countries to limit the vaccine’s use to older people, and a few to drop...
BENGALURU: Three girls suffering from the rare disease, Spinal Muscular Atrophy, were administered the expensive gene therapy, Zolgensma, for free at Bangalore Baptist Hospital on Thursday. Each vial of the one-time...
Click link to visit website https://www.sciencemag.org/news/2021/03/software-engineer-bets-technology-help-speed-rare-disease-treatments Sanath Ramesh’s life took an unexpected turn 2.5 years ago when his son, Raghav Ramesh, was born unable to move his hands and legs....
The disease causes muscle weakness and trouble breathing and can affect the heart and muscles. University of Cincinnati researchers have found a newer, more effective treatment for the disease Pompe that...
With NO support from the government, a faulty gene puts families with #Rarediseases in India, in a never-ending odyssey! Meet the Pompe Warriors, 2 Different Lives, and their unique stories....
