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Hyderabad to host Asian Thalassemia Conclave in January 2026

Focus on making India Thalassemia-Free by 2035

Hyderabad to host Asian Thalassemia Conclave 2026 in January

Dr. S. Sangeeta Satyanarayana, IAS, Commissioner, Health & Family Welfare Dept. & Mission Director (NHM), Government of Telangana to inaugurate the 2 day conclave

DKMS Foundation India to offer free HLA Typing in Punjab under...

The program will prioritise remote and underserved areas, expanding awareness about DKMS Foundation India’s mission, its cause, and its thalassemia program

SOHM secures key patent for revolutionary gene editing technology

Paves way for genetic disorder treatment breakthroughs in India

TSCS participates in Thalassemia Conclave 2024

Dr Chandrakant Agarwal, President, Thalassemia & Sickle Cell Society (TSCS) joined an elite group of panelists to discuss the prevention, diagnosis, management of Thalassemia

MGM Cancer Institute launches Anamaya Program across Tamil Nadu and Andhra...

The initiative focuses on treatment for thalassemia and childhood blood disorders, aiming to improve early detection and care for children

2nd national conference to combat Thalassemia to be held in Hyderabad

Thalassemia and Sickle Cell Society (TSCS) Hyderabad is hosting a national-level conference with participation from international and national experts & speakers

TSCS team meets Dr Bharati Praveen Pawar to urge support towards...

The Minister was extremely impressed by the dedicated service of the society as she spared extensive time to listen to the contribution of TSCS towards Thalassemia

Thalassemia and Sickle Cell Society conducts their Annual General Body Meeting

The AGM had important discussions around making India Thalassemia free through the notable programmes being held by the society

356 bone marrow transplants for Thalassemia patients successfully completed under Thalassemia...

The Coal India CSR-funded Hematopoietic Stem Cell Transplant (HSCT) program is a unique initiative aimed at providing a one-time cure opportunity to underprivileged Thalassemia patients