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  1. Jenny

    This was the only spot I could find a place to leave a comment. Your story has helped me out tremendously! My daughter has not been diagnosed with CP yet but I have a feeling that is where we are headed. It all started when she wasn’t smiling when she was supposed to be. Her doctor kept an eye on here and more and more delays were noticed. We have done a CT and MRI. The only answer I’ve gotten is that she has a very thin Corpus Collosum (which can have results of some form of mental disability). Her neurologist didn’t say antything about it except, there are people that go their whole lives without one and are fine and that he was leaning more towards CP.
    I had a normal pregnancy and she had no problems at birth. After finding and reading your website I have learned that she has a lot of the symptoms to a degree. She didn’t start sitting on her own until she was 10 months, she still does not crawl however, she will get up on her knees and hands and rock. She just turned and year old and she does not talk at all. Just moans here and there. She has low muscle tone and one of her eyes exerts out.
    We are getting things going on the early intervention program and all the therpy will be starting soon. Occupational, Physical and Speech.
    With that said I just wanted to thank you for posting your story as it has informed me much more than the doctors have. I can take this information to get more answers.
    I admire you and your son and your story has truly inspired me!
    I hope to talk to you in the future!

    From Phoenix, Az.,
    Jenny

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