“We serve with passion towards Thalassemia & Sickle cell affected children.”

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Who we are

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Thalassemia and Sickle Cell Society (TSCS) is a registered NGO (Reg. no. 5359 Dt. 22/10/1998) established in the year 1998 with the pledge to help the Thalassemia patients. Thalassemia is a genetic blood disorder and affected patients depend on regular blood transfusion for survival, usually every 2 to 3 weeks. Our objective is to treat all thalassemia children and add years to their lives.

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Our Mission is to give healthy life

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To promote the provision of appropriate treatment and to achieve a good quality of life for every patient with Haemoglobinopathies, and to encourage prevention policies with the aim of reducing the number of newly affected births. To promote research activities for bring-ing newer treatment for thalassemia patient.

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Let’s build the better world together without
starving children, pain and death.

Our Services

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