Thank you for helping Arthur and two other children!

Arthur is only fifteen, but his medical records already show several severe diagnoses. He has critically low levels of all important blood cells, chronic inflammation of the lymph nodes and bronchi, gastritis and many other dangerous complications. All of these are manifestations of his congenital genetic disease - primary immunodeficiency. This is the name of a rare mutation in the genes of the immune system, which systemically disrupts the work of the body. Because of the disease, Arthur spends almost all of his time at home or in hospitals, it is incredibly important for him to avoid all contact. Each accidental infection can literally cost the boy his life. Doctors have managed to find an effective therapy for Arthur, but the family cannot get these drugs at their place of residence yet - it will take months to get the necessary documents. Arthur does not have this time - his disease is rapidly progressing. Dear tubers, we are opening a fundraiser to pay for vital therapy for Arthur and two other children with similar immune pathologies. Let's work together to help them stop the disease!