Milana studies at a regular school, does vocals - everything is like ordinary children, but with one difference: she has epidermolysis bullosa. This is a rare genetic disease that affects the skin, and in severe cases, the mucous membranes. Milashin is just such a case. Therefore, all this “ordinary life” is given to the girl and her family with great daily efforts.
In order for the disease not to destroy Milana's skin, she needs daily dressings, which, in fact, play the role of a second skin. Bandaging for epidermolysis bullosa is similar to a multi-layered pie: atraumatic bandages impregnated with wound healing and antibacterial compounds are applied to damaged areas, the most traumatic areas are protected with silicone or sponge pads, and the bandage itself is fixed with several types of special ultra-soft bandages that "breathe", allow you to move and not rub and so prone to injury skin.
The Butterfly Children Foundation is opening a fundraiser for dressings and care products for Milana. For the Milana family, this is an unbearable amount, for you and me - another good deed!
Verified by Tooba
Verified by Tooba
