The boy has a rare genetic disease - hemophagocytic lymphohistiocytosis. It affects internal organs.
In 2021, when Elaman was only four years old, he received a successful bone marrow transplant. “My son didn’t have a childhood—his illness took him away. While the other children played with friends, walked outside and went to kindergarten and school, Elaman spent time in the treatment room for examinations and chemotherapy,” recalls the boy’s mother.
Now Elaman is seven years old. Last fall he started having problems with the gastrointestinal tract. In March, doctors of the hospital named after Z.A. Bashlyaeva was recommended to undergo three molecular genetic studies. When doctors receive the result, they will be able to adjust the treatment.
However, these studies are too expensive for Yelaman's family. You can help right now!
