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Urgent!
Karol Chłap, 2 years old

The first case of this genetic mutation in Poland! Please save our little son!

Every day, we travel tens of miles to visit our little son Karol, who has been staying in the hospital NICU since he was born in June. Due to his rare genetic disease, we cannot take him home. The hemizygous mutation in the X-linked THOC2 gene causes dysmorphic features associated with hypotonia,...

PLN 37,468
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Karol Chłap is waiting for Your supportYou can help too!DonateDonated by 761 people
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