The Thalassemia and Sickle Cell Society (TSCS), Hyderabad, observed World Sickle Cell Day on 28th June 2025 with a heartwarming and empowering celebration dedicated to children and families affected by Sickle Cell Disease. The event served as a reminder of the strength within this community and the importance of awareness, care, and compassion.
The event began with a gracious Welcome Address by Dr. Chandrakant Agarwal, President of TSCS, who extended his heartfelt greetings to all the attendees. He reiterated TSCS’s steadfast commitment to improving the lives of those affected by hemoglobin disorders and called for greater awareness, early screening, and community participation in addressing Sickle Cell challenges across India.
This was followed by an inspiring Message by Dr. Suman Jain, Chief Medical Research Officer and Secretary, TSCS. Dr. Jain praised the resilience of the children and families present and emphasized the role of TSCS not only in clinical care but also in emotional and social support. She encouraged everyone to continue spreading awareness and standing together in solidarity for a better future.
The program was further enriched by two thought-provoking motivational talks.
Mrs. Surbhi Sharma, Assistant Professor of Law at NALSAR University of Law, who is Sickle Cell Warrior, emphasized the importance of legal empowerment, patients’ rights, and the role of inclusive public policy in healthcare access.
Dr. Subodh Kumar Karmanker, MBBS, RIMS Adilabad, who is Sickle Cell Warrior brought in valuable insights from the field, speaking about the challenges and solutions for managing Sickle Cell Disease, especially in tribal and underserved communities.
Adding joy to the occasion, fun and games were organized for the young patients, filling the room with laughter, excitement, and unforgettable moments. The event was a celebration of life, hope, and togetherness.
As a gesture of love and encouragement, gifts were distributed to all patients, bringing smiles to their faces and making the day even more special for them and their families.
The event saw active participation from around 100 patients and their parents, making it a truly memorable and impactful gathering.
TSCS remains dedicated to its mission of creating a healthier, more hopeful future for individuals living with Sickle Cell Disease, continuing to stand by them with care, commitment, and compassion.
