The news of a difficult diagnosis of a child will frighten and discourage any parent. When Magomed Abakarov's mother found out that her son had dystrophic epidermolysis bullosa, a genetic skin disease that would remain with the boy for life, her first reaction was shock. Tears, despair, not understanding what to do next ...
With this disease, the skin practically does not fulfill its main function - the protection of the body. She is so thin and weak that almost anything can hurt her, even the seams from clothes or shoes. Any movement - and a bubble appears on the skin, which then bursts and leaves a wound behind. That is, the skin itself needs protection in the form of special ointments, bandages and dressings.
Since Magomed has the most severe form of the disease, dystrophic, almost his entire body is covered with such bandages.
Today Magomed is already 12 years old. Most of all he likes computer games. In virtual reality, he can do what he cannot do in ordinary life: travel, run towards adventures, achieve any goals.
Mom says that Magomed is a very kind boy and is always ready to help. But Magomed's fingers grew into a fist, because the skin between them was in constant wounds and now many things are difficult for him.
To prevent this from happening, the wounds do not become inflamed or wet, the skin needs proper care. In Magomed's case, these are daily dressings using special fixing dressings and elastic bandages, treatment of damaged skin with mild antiseptics and healing ointments.
The dressing is done by Magomed's mother. Seeing how much money is required, she is very afraid that she simply will not be able to pay for another set of vital medicines and bandages for her son.
297,085 rubles - this is exactly how much needs to be collected now in order to provide the boy with elastic bandages, fixing bandages, gels and creams for 1 month.
Magomed's mother faces this unbearable amount every month from year to year.
Now together we can give the boy one more month without pain, and mom a month of respite. Your help and support is needed now more than ever!
