Elena received the necessary bandages and skin care products!

Elena, a ward of the Butterfly Children Foundation, is in her early 30s. She is a beloved wife and mother of two wonderful children. But her diagnosis — dystrophic epidermolysis bullosa — overshadows the fragile family happiness. Patients with this rare incurable skin disease are called "butterflies" because of the thin and fragile skin that requires daily dressings. In recent years, Elena's condition has worsened, the disability group has changed from the second to the first. The situation is aggravated by tooth loss, hair loss and problems with nail plates. The resulting high temperature has to be removed with antibiotics and painkillers. Elena does not go a day without bandages. The situation is complicated by the fact that ordinary bandages are not suitable for "butterflies", they need special expensive bandages and bandages for daily care. The Butterfly Children Foundation opens a collection for Elena for bandages and skin care products. Let nothing stop her from spending time with her family, hugging her children and enjoying every day!