Thalassemia & Sickle Cell Society

Thalassaemia and Sickle Cell Society (TSCS) is a registered (Reg No. 5359) non-profit, non-governmental organization founded in 1998 representing mainly by a small group of patient’s parents, doctors, well-wishers, philanthropists, etc. to provide the best treatment and management to patients suffering from Thalassemia and Sickle Cell Anemia. Ever since we started, our priority has always been to improve our services provided to patients in accordance with the latest developments in treatment, management, and prevention of the same.