In India, Parents of Children with Rare Disease Plea for Help Online
India makes many of the world ’s drugs, but treatments for rare diseases like spinal muscular atrophy are imported and prohibitively costly. In desperation, parents are raising funds on social media.
Source: NYT Health - Category: Consumer Health News Authors: Sameer Yasir, Shalini Venugopal Bhagat and Sara Hylton Tags: India Spinal Muscular Atrophy Drugs (Pharmaceuticals) Crowdfunding (Internet) Parenting Biogen Inc Novartis AG Roche Holding AG Babies and Infants Children and Childhood Source Type: news
More News: Babies | Children | Health | India Health | Internet | Parenting | Rare Diseases | Spinal Muscular Atrophy