TSCS appeals to the Govt. of Telangana to release a G.O for mandatory antenatal test - HbA2 for every pregnant woman to help prevent the birth of Thalassemia Major Children for the well-being of their family & Telangana State
Left to Right: M A Aleem Baig, Joint Secretary, TSCS, Ratnavali Kothapalli, Vice President, TSCS, Chandrakant Agarwal, President, Thalassemia and Sickle Cell Society (TSCS), Dr. Suman Jain, Secretary & CEO, TSCS, Naresh Rathi, Chief Patron, TSCS
Thalassaemia and Sickle Cell Society (TSCS) a registered non-profit organization has announced to organise First-of-its-kind National Level Conference on Prevention of Thalassemia and Sickle Cell Anemia on 30th April & 01st May 2022 at TSCS, Hyderabad. TSCS has taken the initiative of inviting all Thalassemia societies from across 23 states of India for the conference to discuss the strategic steps for the Prevention of Thalassemia and Sickle Cell Anemia.
Harish Rao, Hon’ble Health Minister - Government of Telangana will be the Chief Guest for the National Conference. There will be a participation of more than 200 delegates who would chalk out a road map on preventive measures for the genetic blood disorder - Thalassemia at the National Conference. TSCS is also appealing to Harish Rao, Hon’ble Health Minister - Government of Telangana to release a G.O for mandatory antenatal test - HbA2 for every pregnant woman in the first trimester of pregnancy.
TSCS is the world’s biggest society serving more than 3000 Thalassemia Children with modern equipment & specialist doctors, Free of Cost in Hyderabad. TSCS Free services includes Doctor Consultation, Free Laboratory investigations (CBP), Medicines, HLA test, HbA2 test of parents, siblings and extended family members, Blood transfusion and Free Bone Marrow Transplant with the help of Bajaj Electronics, Hyderabad,. With an aim to make “Thalassemia Free Telangana”, TSCS has recently opened its first branch in Khammam with well experienced medical staff to support Thalassemia and Sickle Cell Anemia patients in the region and nearby districts. The staff at TSCS is working relentlessly realising the physical & mental pain of Thalassemia patients, as their own family members/friends are affected by Thalassemia.
Speaking on the occasion, Chandrakant Agarwal, President, Thalassemia and Sickle Cell Society (TSCS) said that “It is truly an encouraging occasion for us to organise a National Level Conference on Prevention of Thalassemia and Sickle Cell Anemia for the first time in India and in Hyderabad. The need of the hour is to create further awareness among the masses on the importance for HbA2 test for everyone. TSCS would sincerely request Govt. of India to pass a Bill for making it mandatory for every couple in India to go for HbA2 test before pregnancy or first trimester of pregnancy. Let’s all take a pledge of being a responsible citizen to educate the people about genetic blood disorder - Thalassemia and eradicate this disorder and make India a Thalassemia Free country.
Dr. Suman Jain, Secretary & CEO – TSCS said “Bone Marrow Transplant the only ultimate Cure for Thalassemia and TSCS is working interminably for the extinction of Thalassemia for the past 24 years, it is only possible with the government’s support. About 4 per cent of the population are Thalassemia carriers and around 10,000 children are born Thalassemia major in India.”
Ratnavali Kothapalli, Vice President, TSCS sharing her comments said “We are extremely honoured to be hosting such a conference at a national scale in Hyderabad.”
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