This is the story of our child Kirill. Kirill has a rare genetic disease - CTNNB1 syndrome. This syndrome is characterized by the presence of a disorder of the musculoskeletal system, cerebral palsy, partial atrophy of the optic muscles, congenital cataract, alternating convergent strabismus and other diseases and disorders. With all this, Kiryusha is a very mobile, inquisitive and very active child, he does not want to sit still for a minute and wants to constantly move. We do our best to help him in development, investing ourselves in it, doing everything possible and impossible in order to achieve rehabilitation, treatment, classes. And on this channel we want to share at least a part of what is happening in the life of a special child, maybe someone will find these videos interesting and useful in terms of studying the characteristics of children with CTNNB1 syndrome. Subscribe, like, we will be grateful for your support and help. Kirill help group: vk.com/pomoch_kirillu