Thalassemia and 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.
With the objective of helping all of our Thalassemia and Sickle Cell Anemia affected children, TSCS has established, well-maintained transfusion centre, high-quality blood bank, modern diagnostic laboratory, and advanced research centre under one roof to support more than 2800 registered patients for the past 22 years.
TSCS provides free consultation, free blood and transfusion facilities, unselling, investigations, and food for around 45-50 patients daily. We are proud to have eminent doctors, specialists, hemato-oncologist, pediatric endocrinologists, cardiologists, pediatricians, pathologists, ophthalmologists, dentists, radiologists, and research scientists associated with us in helping to provide the best comprehensive care and cure for our patients.
TSCS is putting its heart and soul into getting BMT (Bone Marrow Transplantation is the only cure for Thalassemia) done for the patients by doing free HLA typing, counseling them for BMT, and helping them financially. Which is a great social, mental and emotional support and relief to the family.