Ahmad received a supply of bandages!

Ahmad is 19 years old, he has a severe dystrophic form of epidermolysis bullosa (EB). Due to a genetic breakdown, the guy has a very vulnerable skin and mucous membrane. One awkward movement or eating too hard - and wounds form on the body, in the mouth or on the esophagus. Ahmad grew up in the outback, where no one knew anything about his rare diagnosis. My parents did everything they could, but ordinary bandages only hurt the skin even worse. "Clothes often stuck to bandages, and bandages to wounds. My mother and I sat and tore it all off for several hours - both clothes and bandages," Ahmad recalls. Ahmad's mother has been praying for her son's healing for many years. And then she began to pray for relief from his suffering. "At that moment, the Butterfly Children Foundation appeared in my life. I remember how people came with medicines, bandaged me, explained everything, my mother sat, listened and cried with happiness. From that moment on, my life changed," says Ahmad. A bandage for epidermolysis bullosa looks like a multi-layered pie. The problem is that each component of this "pie" is a high–tech, expensive medical device, and bandages need to be changed daily. The cost of dressings in severe cases, like Ahmad's, reaches several hundred thousand rubles per month. "My whole past life was pain and fear of bandages," says Ahmad, "Today I do bandages with joy. A few years ago, I could not have imagined such a thing." To relieve a person from the pain that he has been experiencing for many years is a huge celebration. Support the collection for bandages and care products for Ahmad, let his holiday continue!