Thalassemia is the most common single gene disorder in humans. It is estimated that about 300,000 babies are born every year with major hemoglobinopathies around the world. In Thalassemia, the life span of the red blood cells significantly reduces because of ineffective hemoglobin synthesis. Children affected by this disorder become transfusion-dependent for the rest of their lives. It is recommended that children with sickle cell anemia, hemolytic anemia and bone marrow failure should undergo regular blood transfusion to maintain their hemoglobin levels.
- Coordinate with blood banks for providing regular transfusion services.
- Provide free medical checkup for affected children regularly.
- Provide Leukocyte filters for transfusion to affected children at concessional rates.
- Free Diagnostics tests for affected children during medical camps.
- Awareness and educational programs in and around Hyderabad.