Thank you for helping the kids!

“Timurchik is our main happiness, our hope. Our life!” - says Gulminat about her son. Before the birth of the boy, the family went through incredible pain - three of their children died before they had even lived six months. Each of them had congenital immune abnormalities, which were discovered posthumously. In Russia, correct diagnosis is delayed by an average of 5 years. Children with severe forms of the disease simply cannot be helped in time. Timur has every chance to live a long and full life. Doctors know for sure that the boy has a congenital genetic breakdown of the immune system. At the age of three months, the baby underwent a bone marrow transplant, thanks to which Timur's condition stabilized. Now it is important to understand how far the donor cells have taken root and what replacement therapy will be most effective for the boy. Only expensive genetic analysis can show this. Dear tubers, we are raising funds for important genetic diagnostics for Timur and other children with severe immune pathologies. Please support our collection!