Collection for special dressings for Ahmad with epidermolysis bullosa

A 21-year-old young man has a severe form of a rare genetic disease – epidermolysis bullosa. His vulnerable skin can be injured by the slightest careless touch, which is why people like Ahmad are called "butterflies."

When he was born, doctors knew almost nothing about this disease. Intuitively chosen treatment in childhood only worsened Ahmad's condition. Mom bandaged his wounds with an ordinary gauze bandage, although this cannot be done with epidermolysis bullosa.

It was only when the family found out about the Butterfly Children Foundation that the young man got access to high-quality medical products for the first time. Bandages began to take place faster, and there were fewer wounds.

But the stock of bandages is quickly running out, and it is difficult for a family to buy them on their own because of their high cost. Therefore, we are opening a collection to ensure continuous skin care for Ahmad.

Support the young man to prevent the exacerbation of the disease and the development of complications!