Almaz now has important medications! Thank you!

Until his twenties, Almaz's life was happy and full - family, friends, his favorite cyber sport and big plans for the future. But a year ago everything changed. The guy was found to have a rare genetic mutation - congenital immunodeficiency. The disease suddenly manifested itself with weakness, shortness of breath, a series of pneumonias, bronchiectasis (purulent inflammation) in the lungs and critically low hemoglobin level, because of which only recently Almaz has had 39 blood transfusions. In the hospital the boy's condition was stabilized thanks to effective supportive therapy. But Almaz cannot receive this treatment at his place of residence yet - it will take months to formalize his disability. The young man does not have this time. Dear tubers, we are opening a collection to support Almaz - to buy and deliver for him a course of vital treatment. Let's together help the boy to regain his full life!