Grisha is a cheerful 10-year-old boy. He was born on the appointed date and day. After discharge, worries began. Crying, refusing to feed, not focusing the eyes, lagging in development. At 5 months old, the first attack of epilepsy occurred.
Only by the age of 5, the boy was diagnosed with a rare genetic disease: a deficiency in glucose transport to the brain, which is aggravated by epilepsy, ataxia, and delayed physical, mental, and speech development. A ketogenic diet is recommended.
Thanks to regular rehabilitation, Grisha is able to sit, stand at the support, and move independently on a flat surface.
Now Grisha needs to work with balance and a defectologist using the pex method, the boy does not speak, but understands the addressed speech.
Let's help Grisha run, jump and communicate with peers on equal terms!
Спасибо огромное всем
Спасибо дорогие♥️