Mohammad-Amir is fascinated by virtual worlds - in them he can be a mighty warrior, a brave soldier, or innocently collect castles from cubic blocks: it all depends on the icon on the screen, which he decides to click on. Computer games usually displease parents - the child forgets about school and does not breathe fresh air. Here are just "shooters" and "rpg", as the older generation calls them out of habit - this is not just a way to distract from the lessons and "score on homework." For a 12-year-old boy, this is one of the few ways to forget about pain and feel like one of the millions of ordinary boys.
Mohammad-Amir is a “butterfly child”. It sounds like something from these very games, but this diagnosis is not at all an ability in the game that can be replaced. This genetic and incurable disease is epidermolysis bullosa. The boy is let down by his armor - leather. Any careless movement threatens to result in injury. First, a small bubble will appear, the skin will swell, and then the wound will open.
Mohammad-Amir has a severe form of epidermolysis bullosa. Because of this, he cannot go to school and is homeschooled. He is surrounded by the care of his loved ones - mom and dad and older brother and sister. And he loves to please them - the second main hobby of Mohammad-Amir was cooking, the boy loves to cook.
But in order to take up any of his hobbies, he needs serious preparation - the skin must be treated with creams and ointments, and constantly bandaged. This requires bandages that are suitable for the needs of people with epidermolysis bullosa - they allow the skin to breathe, while - they do not chafe or injure the child.
We can help Mohammad Amir with the necessary medicines, which will last for two months.
