You helped Khalisa and Bilal! Thank you!

Constant infections, stomatitis, otitis media, abscesses (pustules) and pneumonia - since birth, three-year-old Khalisa has been battling the effects of a dangerous and rare disease. Recently we raised funds on Tuba for genetic analysis for the little girl. And thanks to your support Khalisa was diagnosed correctly! The study confirmed that the girl has a congenital mutation - primary immunodeficiency. This means that the little girl's body is unable to resist any, even the most harmless infections. According to the results of the study, doctors adjusted Khalisa's therapy - she needs to take immunoglobulins - donor antibodies on a permanent basis, which will fill in the gaps in her own immunity. The girl's mother has already filed documents for disability registration and an application for discounted medicines. All this will take months, and Khalisa has no time to wait - she needs therapy now, otherwise it will be impossible to achieve positive dynamics. Dear Tubers! Another ward of the Foundation - two-year-old Bilal - is in a similar situation. The boy also needs expensive substitute medicines. We are collecting funds to buy life-saving therapy for Khalisa and Bilal. Let the two adorable kids have a chance to defeat a dangerous disease and regain their childhood without pain.