Eight-year-old Muhammadayub has primary immunodeficiency - a rare congenital defect in the immune system gene. The child's body is defenseless against infections and is at high risk of developing cancer.
Since birth, Ayoub has been sick often and for long periods of time. Otitis, pneumonia, bronchitis - literally every month the boy is hospitalized with another infection. The genetic disease has also affected the child's nervous system. Muhammadayub was diagnosed with ataxia - a severe disorder of movement coordination.
Dear tubers, recently you have already helped Muhammadayub and paid for life-saving medicines for him! Very soon he will start receiving these therapies. But the problem is that these medicines will be enough only for a while, and it is impossible to interrupt the treatment in any case, otherwise all the positive effect will be nullified.
And while there is no hope at all that the family will soon start to receive subsidized medicines, we are collecting funds for a six-month course of vital treatment for the child. We really want to support Ayub and raise funds to pay for his further treatment. May the boy be safe!
Да исцелит тебя Всемогущий Своим Наилучшим Исцелением ! Амин !
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