Little Sumaya received medicines and dressings that are important for her skin!

Little girl Sumaya, she is three years old, and, like any of her age, she loves soft toys. Among the favorites is the unicorn, a fabulous beast that is so hard to find. A unique magical friend - a unique girl. If she lived in a fairy tale, her diagnosis of a butterfly child would mean that she is a fairy or a sorceress, maybe a friend of Peter Pan. But the world is far from good stories about wonderful worlds - behind the words "butterfly child" hides a terrible disease, epidermolysis bullosa. This is a very rare and currently incurable disease. Due to the breakdown of genes, the skin ceases to protect the body - it itself requires protection. From any touch, a severe, painful and non-healing wound can remain on it. But the diagnosis of epidermolysis bullosa is not a sentence. Sumaye requires daily dressings. This is a long and complicated process - ordinary bandages are not suitable, they will only damage the delicate skin. We need special products, creams and ointments - unique drugs are very expensive. Thanks to your help, the Butterfly Children Foundation will be able to help a little girl. Our specialists will assemble a box with everything you need so that Sumaya can forget about pain for two months.