Azinat is a little over a year old. The girl was born with a rare genetic disorder — epidermolysis bullosa. With this condition, the skin is particularly vulnerable: even slight friction can lead to blisters and injuries.
“Her first wounds appeared when she was three months old,” says Azinat’s mother. “Gradually, they started appearing on her legs, abdomen, and back. Azinat started crawling on time, but she’s still afraid to walk. She wakes up at night because of itching. We really hope that specialists will help us find a therapy for her.”
Currently, it is important for Azinat to undergo an examination by specialists in rare skin diseases. The doctors will be able to assess her condition and adjust her therapy and care.
Along with Azinat, three other beneficiaries of the foundation with bullous epidermolysis are also waiting for help.
Support the fundraising with any amount that is convenient for you. Your donation will help the children reach the specialists and receive the necessary medical care.
Verified by Tooba
Verified by Tooba
