Abdulaeva Khadizhat is a simple 14-year-old girl from Dagestan. She loves to cook pancakes and draw - like many of her peers.
But, sharing hobbies and interests with her friends, she is very different from them: the girl is called a “butterfly”. Doctors diagnosed her with epidermolysis bullosa. This is a rare and currently incurable disease. Due to the “breakdown” of genes, the skin ceases to perform one of its main functions - to protect the child. Blisters form at the site of a careless touch, which turn into painful wounds. They must be immediately disinfected and bandaged, otherwise the wounds become easily infected.
Khadizhat's disease is severe, dystrophic. Serious complications came along with epidermolysis bullosa. But the girl does not despair, and, as her mother says, she loves people very much.
She needs special dressings - soft breathable bandages, silicone pads, non-traumatic wipes, alcohol-free antiseptics. Ordinary bandages will not work - they stick to the skin and come off with it. Such funds are very expensive - and most of the parents' income goes towards buying them.
Our common help will help the girl to live without pain for two months and enjoy life!
