Hello people
I am a 25 year old who was diagnosed with CP at 6 months. I have a mild form of cp. I have gone through some hard times when I was a child and live in a place where i am the only person with CP. I have a different perspective on the disease. I am writting on this forum because I love to help people and anything I can do to help other people with CP and get them through those hard challenging times is my goal. So If you would like the perspective of a 25 year old please write me any questions you might have and I will answer them the best I can.

