Halisa has primary immunodeficiency and requires replacement therapy

Constant infections, stomatitis, otitis, abscesses, and pneumonia — since birth, five-year-old Khalisa has been fighting the consequences of a dangerous and rare disease. Genetic testing confirmed that the girl has a congenital mutation — primary immunodeficiency. This means her little body is unable to fight off any infections, even the most harmless ones. Right now, Khalisa is experiencing a severe exacerbation: doctors have diagnosed her with three serious conditions at once — pneumonia, otitis, and reflux. To cope with this blow and save the girl, she urgently needs a course of life-saving medication — immunoglobulins (donor antibodies) that will fill the gaps in her own immune system. The girl's mother has already applied for subsidized medications, but the paperwork will take months to process. Khalisa doesn't have time to wait: she needs therapy right now to overcome this dangerous exacerbation and achieve positive progress. Dear Tubers! We are raising funds to purchase life-saving treatment for Khalisa. May she have a chance to defeat this dangerous disease and reclaim a childhood without pain.