Hope in every ticket: support for Aliya and other wards with rare diseases

On January 13, Aliya turned 1 year old. When remembering the day her daughter was born, her mother Saida can't hold back tears: the baby had no skin on both feet. The diagnosis was quickly established: epidermolysis bullosa.

Aliya needs regular bandages. And now hospitalization will be required to be examined, to assess how Aliya is developing, and to adjust her care.

The Butterfly Children Foundation is opening a collection so that Aliya and her mother and four other foundation wards with their parents can get to the hospital or sanatorium and then return home.

Regular hospitalization and rehabilitation make it possible to consolidate the results of treatment – this is what makes it possible to minimize the manifestations of the disease and live a normal child's life.

We can help them together!