Usman needs a genetic study to fight cancer!

Usman is only two months old. He is the firstborn and very much awaited.

The baby was diagnosed with: rhabdomyosarcoma of the presacral region with spread into the abdominal cavity. The pregnancy went normally, all necessary screenings were completed in full — no pathology was suspected. The disease was discovered only after the birth of the son.

Usman is currently being treated at the NMITs of Oncology named after N.N. Blokhin. The parents are endlessly grateful to the attending doctors: during the course of therapy, the child has noticeably improved, and he is gaining more and more strength. The fight continues, and it is bringing results.

But the treatment cannot be stopped. In order to select further therapy, a genetic study is needed: it will help determine the cause of the immune disorder. The family cannot afford to pay for it — the mother is in the hospital with her son and physically cannot work.

Let us support Usman and his parents and raise funds for this vital study.