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!
