“My name is Chandrakant Agarwal, and my life’s motto has always been ‘live and let live’. As the President of the Thalassemia and Sickle Cell Society (TSCS), an organization dedicated to the support, treatment, and advocacy for individuals affected by thalassemia and sickle cell disease, I have dedicated my efforts to improving the lives of children suffering from Thalassemia and Sickle Cell Anemia. This journey began with a personal conviction and has shifted into a mission that has garnered national recognition.

I come from a family that migrated to Hyderabad from Singhana, Rajasthan, nearly a century ago. Hyderabad has been our home ever since, and it is here that I have built both my business career as Chairman of the Navadurga Group of Industries and my philanthropic endeavors.

The story of TSCS began in 1998. It was founded by a small group of patients, doctors, well-wishers, and philanthropists who were determined to provide the best treatment and management to patients suffering from these severe blood disorders. Over the past 25 years, we have grown exponentially, now serving over 3600 children every day. Our facilities include a high-quality blood bank, a modern diagnostic laboratory, and an advanced research center. These services are provided free of charge to ensure that every child receives the care they need.

One of the most significant achievements in my journey was receiving the ‘Samaj Gaurav’ award, recognizing our relentless work. But the true reward comes from the smiles and improved health of the children we help. Our mission has expanded beyond Telangana, reaching into Tier-2 markets and forming a national network with various partners.

Awareness and prevention are crucial. We have been actively educating the public about the importance of antenatal testing and advocating for better support for genetic disorders. The Thalassemia situation in Telangana is dire, and the introduction of a Government Order (GO) for antenatal testing is essential. With proper legislation and support, we can significantly reduce the incidence of this disorder and ensure proper treatment for those affected.

My journey with TSCS is driven by a simple belief: that together, we can make a difference. We are committed to continuously improving our services, embracing the latest advancements in treatment, and striving to make our state and country Thalassemia-free. This is not just my story; it is the story of every child we help, every family we support, and every step we take towards a healthier future.”