Oisha was born on March 22, 2025. The girl has a severe form of epidermolysis bullosa. This is a rare genetic disorder in which even a simple touch can cause serious skin damage.
Oisha's mother, 22-year-old Shukrona, every day, she carefully processes her daughter's skin and makes complicated dressings according to all the rules. It takes a lot of time and requires a lot of patience. Shukrona is scared, but she believes that with the help of doctors and kind people who care, she and Oisha will overcome all difficulties.
To protect the skin, special dressings are needed: soft non-woven napkins, silicone bandages, fixing atraumatic bandages. There are also therapeutic creams and ointments that help reduce inflammation and keep the skin as healthy as possible. All this is vital so that the girl does not get hurt, so that she can move, reach for toys, explore the big world.
By supporting this collection, we are helping Oisha to live her little life a little more calmly and safely. Let there be less pain and more space to just grow and enjoy everything around you.
