Rare disease patients demand compulsory licensing for life-saving drugs: Here’s why it’s significant | Health and Wellness News
For Seba P A, 26, from Kerala, the cost of breathing easy, moving around and enduring fewer bouts of infection comes at a steep price — nearly Rs 18 lakh per month. For long, she had managed with the Rs 50 lakh government grant under the national policy of rare diseases, one of which —