Since his birth, Muhammad has been fighting an endless series of severe and dangerous diseases. Pneumonias, inflammation of the intestines and bladder, congenital heart defect, dropsy, multiple cysts, ear and joint surgeries - only a small part of what the child had to face. Muhammad is stunted in growth and development, he has great difficulty with the program of even a specialized remedial school.
Doctors assume that all these manifestations are symptoms of a congenital genetic disease - primary immunodeficiency. This is a rare random mutation that systemically destroys the boy's body. Only expensive high-tech research can confirm and clarify this diagnosis. Its results will tell doctors how to properly, effectively and safely treat the child.
Dear tubers, please help us raise money and pay for important genetic tests for Muhammad and two other children with suspected immunodeficiency. Let's give three little sunflowers a chance for a future without pain!
