With two CP special needs kiddos in the house we're super busy. Lili (and Jo) goes to her special preschool 4x a week. Both her and CJ get OT and PT 2x a week each. We're going to start going to a special CP clinic at the local children's hospital 1x a month. We'll see a lot of specialists all in one afternoon. I'm learning more and more about CP.
In the United States today, more people have cerebral palsy than any other developmental disability, including Down syndrome, epilepsy, and autism. Although children with very mild cerebral palsy occasionally recover by the time they are school-aged, cerebral palsy is usually a lifelong disability. In most cases, the movement and other problems associated with cerebral palsy affect what a child is able to learn and do to varying degrees throughout their life.
CJ has Spastic Cerebral Palsy (stiff and difficult movement)
Lili has Ataxic Cerebral Palsy (disturbed sense of balance and depth perception)
Both of their cerebral palsy may be the result of an injury to their brain before, during, or after birth. In Lili's case, as a very premature baby, bleeding into the brain (intraventricular hemorrhage) caused extensive damage. I think in CJ's case nuerological damage was caused by toxic injuries, or poisoning, from alcohol or drugs used by the mother.