“I’ve always believed in one simple idea — live and let live. That belief shaped not just my life, but the work I chose to dedicate myself to.

As the President of the Thalassemia and Sickle Cell Society (TSCS), my journey began with a personal conviction and slowly grew into a mission that now reaches thousands of families across the country.

I was born in Hyderabad to a family that migrated from Rajasthan nearly a century ago. This city shaped both my business journey, as Chairman of the Navadurga Group of Industries, and my commitment to social responsibility. TSCS was founded in 1998 by a small group of patients, doctors, and philanthropists who came together with one shared goal — to ensure quality care for children living with thalassemia and sickle cell disease.

Today, TSCS supports more than 3,600 children on a daily basis. From a high-quality blood bank and modern diagnostic laboratory to advanced research facilities, all essential services are provided free of cost to those who need them most.

What truly keeps me going is something simple — the smile on a child’s face when they receive timely care. Over the years, our work has expanded beyond Telangana, helping build a national network while also focusing on public awareness, especially around antenatal testing and early diagnosis.

The thalassemia situation in Telangana remains a serious concern. Introducing a Government Order for mandatory antenatal testing is a crucial step forward. With the right policy support and awareness, the number of affected children can be significantly reduced, while ensuring better treatment for those already living with the condition.

My journey with TSCS is guided by a strong belief that the meaningful change is possible when people come together. This is not just my story. It belongs to every child we support, every family we stand beside, and every step we take towards a healthier future.”

— Chandrakant Agarwal
President, Thalassemia and Sickle Cell Society