Children with epidermolysis bullosa were examined and received the prescribed treatment!

16-year-old Vitya has a dystrophic recessive form of epidermolysis bullosa and a severe course of the disease. This genetic skin disease is currently incurable, but with strict adherence to the care regime and competent dressings, which patients need daily, timely hospitalization and systematic examinations, it is possible not only to prolong life, but also to delay possible disability (finger fusion, joint deformity, etc.). However, the manifestations of this disease are not only external. Epidermolysis bullosa has a negative effect on internal organs, mucous membranes, body systems, and causes multiple caries. Victor and ten other wards of the Butterfly Children Foundation need to undergo examinations and prescribed treatment. Together we can help these children!