I never post on any websites or blogs, but your search is very dear to my heart. I too had a child with very mild C.P., and he was not diagnosised until he was 3 years old.
My son Matt, wore AFOs for several years, sent a lot of time in speech, O.T., P.T.
therapy, and still walks with a gait to date.
He also, is legally blind. The reason for sharing this information is to let everyone
know that there is HOPE for these children.
We always knew that Matt, never would be an athlete or fit in with the rest of the children, so my husband and I tried to do things to make him look as normal as possible. Started at any early age exposing him to other children. Birthday, holiday parties, etc. at our house. Made sure all the kids in the neighborhood felt welcomed. My advice to you would be to concentrate on academics and enroll him in a music program.
And, encourage any accomplishes no matter how small.
Matt, currently is enrolled in the honors program at Southern Methodist University, was "Who Wants to Be a Millonaire", and was on "Beauty and the Geek" last spring.
In those times of feeling alone and not knowing what to do, trust your heart, and never ever give up on your child.
Hope this helps.

Hi, my 9mnths old boy has been recently diagnoised with Cp but it's still to early to say if it's mild or not.Im also looking for perents with kids who have CP.I live in the Johannesbur area and a young mom,this has been very hard on me and im tryig by all means to give my boy a better life.I need to prepare myself and need as much info as possible.talking to a perents would help me a lot.thanking you in advance