Eight-year-old Ismail Elizarov from Orel is a kind and friendly boy. He likes to walk, regrets and feeds homeless cats, is fond of cars. This description is not much different from the words that any of his peers can receive in his address - only Ismail's life, unlike most other guys, is associated with daily overcoming of difficulties.
He is a butterfly boy. So called people suffering from bullous epidermolysis, a rare genetic disease. The innocent name came from the fact that the skin of such people is fragile, like butterfly wings - it practically does not fulfill its main function, does not protect a person. And any touch to it threatens to turn into a serious injury: first blisters will appear, and then they will turn into non-healing wounds.
To avoid this - and give Ismail the opportunity to live the life of an ordinary boy - long daily dressings are required. These procedures are also complicated by the fact that ordinary bandages are not suitable for them; special dressings are needed that will not damage fragile skin. And besides these expensive products, creams and ointments are needed that will restore and protect the skin.
With your help, the Butterfly Children Foundation will be able to collect all the necessary medicines and funds and send them to the family, which means giving Ismail the opportunity to forget about the pain for a while.
