From day one, Aisha's life was at risk. She was born the youngest of twins, weak and premature. Lung and heart problems, underweight, headaches, hair and nail loss, shortness of breath, and critically poor blood tests were just a fraction of what the little girl had to face.
By a year old, Aisha's medical records already included two rare and severe diagnoses - primary immunodeficiency and primary ciliary dyskinesia. Both of these diseases are genetic, congenital. The first affects the immune system, making the girl absolutely defenseless against any infections. And the second - causes severe pathologies of internal organs and affects development.
In her four years, Aisha is gradually making great strides - already a year as the little girl has learned to walk, hold in her hands non-heavy objects and peculiar, but express their thoughts in words. Doctors are convinced that the girl needs long-term substitution therapy, which will stop the development of complications and give Aisha the opportunity to develop.
We are raising funds to pay for life-saving treatment for Aisha and Timofey, another child with a similar genetic pathology. Dear tubers, please support our collection - let two children at once have a chance for a future without pain!
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