Support education for families with children with Spina Bifida and the professionals who help them

Eight-year-old Abram has a congenital disease, spina bifida. When his parents first encountered the diagnosis, they had many questions: how to help their son develop, how to organize proper care, and where to find reliable information? The educational programs at the Spina Bifida Institute helped the family better understand the diagnosis and confidently care for their child.

Not only parents but also specialists gain knowledge that can be immediately applied in practice. The results are the result of the daily work of the Institute's director: creating and developing courses, working with experts, updating educational materials, and organizing training.

Support the project so that the Institute can continue to educate parents and specialists and help children with spina bifida receive the right support.