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Sathvik is suffering from Major Thalassemia. He is 11 Years old and based out of Guntur, Andhra Pradesh. Parents are small private job holders earning 18000/-p.m. and not in a position to bare monthly medical expenditure of their son. Seeking help from any Donors for either operation or for monthly medical
expenses.
expenses.
Name: K. SATHVIK
Father Name: K. Prasad
Address: D.No.15-7-112, Kummara Bazar, Guntur
Contact No: 9949524047
Disease: Thalassemia Major
Treatment - Life long - Weekly once Salined Blood transfusion (350 - 500 ml)
Hospital & Doctor giving treatment: Dr. R. VARADARAJAN, Senior Consultant, Kanchi Kamakoti Childs Trust Hospital, Chennai
Permanent Solution - Bone Marrow Transplant Operation – Need Donor - As both the parents Hematopoietic cells didn’t get match with kid.
Blood Group - O Positive (O+)
Estimated cost of Operation: 35 - 40 Lakhs
About Disease: Thalassemia Major occurs when a child inherits two mutated genes, one from each parent. Children born with Thalassemia Major usually develop the symptoms of severe anaemia within the first year of life. They lack the ability to produce normal, adult haemoglobin and experience chronic fatigue. Regular blood transfusions are the only treatment available to patients with thalassemia.
Father Name: K. Prasad
Address: D.No.15-7-112, Kummara Bazar, Guntur
Contact No: 9949524047
Disease: Thalassemia Major
Treatment - Life long - Weekly once Salined Blood transfusion (350 - 500 ml)
Hospital & Doctor giving treatment: Dr. R. VARADARAJAN, Senior Consultant, Kanchi Kamakoti Childs Trust Hospital, Chennai
Permanent Solution - Bone Marrow Transplant Operation – Need Donor - As both the parents Hematopoietic cells didn’t get match with kid.
Blood Group - O Positive (O+)
Estimated cost of Operation: 35 - 40 Lakhs
About Disease: Thalassemia Major occurs when a child inherits two mutated genes, one from each parent. Children born with Thalassemia Major usually develop the symptoms of severe anaemia within the first year of life. They lack the ability to produce normal, adult haemoglobin and experience chronic fatigue. Regular blood transfusions are the only treatment available to patients with thalassemia.
