You paid for vital genetic testing for Umar and 5 other children. Thank you!

Five-year-old Umar has a thick medical file with dozens of diagnoses, tests and assumptions. But it is still unknown what exactly the boy is sick with. Since birth, Umar has been sick often and for long periods of time - tonsillitis, streptoderma, candidiasis, laryngitis, flu and endless acute respiratory infections. “Every two weeks something new. We just get cured and then we go to the hospital again,” says her mother Ida. Only recently, experts at the Rogachev Medical Center in Moscow suggested that the cause of all this may be a congenital systemic disease - primary immunodeficiency. This is a rare genetic mutation that weakens immunity and affects the work of many organs. Confirm and clarify this diagnosis can only expensive high-tech genetic research. Based on its results, doctors will be able to choose an effective therapy for Umar and give a prognosis for the course of the disease. Dear tubers, we appeal to you for support! Please participate in raising funds to pay for genetic tests for little Umar and five other children with similar symptoms. A correct diagnosis is the first and incredibly important step on the road to recovery!