Magomed Bagomedov is an ordinary guy with ordinary boyish hobbies and activities that often become impossible due to his illness - epidermolysis bullosa.
Magomed has been learning to live with this incurable genetic disease for 20 years. His skin is very fragile, anything can seriously injure her: careless movement, light blow.
So that the wounds do not hurt and they do not get an infection, Magomed needs to wash them every day with a special antiseptic, then apply healing ointments and cover them with soft viscose bandages. They form a protective framework on the skin, thanks to which Magomed can spend a day without pain and the appearance of new wounds.
Illness often stops Magomed on the way to his dreams, even a walk or a trip is a test for him: clothes and shoes often rub the skin, an inadvertent fall on the street, rubbing against the handrail in transport leave wounds.
Despite all the difficulties, Magomed is very happy when he manages to get out of the house and go somewhere. Now she and her mother are going to Kislovodsk for treatment. Magomed is very afraid that the trip will fail, because dressings and necessary medicines may not be enough, and on the road they need much more than at home.
Magomed has the most severe form of epidermolysis bullosa - dystrophic, wounds cover almost his entire body. Dressings are required every day, sometimes several times a day, so the consumption of special medications and bandages is very high. The amount of 296,000 rubles is enough to buy Magomed everything he needs for skin care with a 1-month margin.
This will help him not only not to feel pain and do his usual things, but also to go with his mother for treatment, which he is looking forward to.
