Second day of school for this week and of course Hannah is very tired but she is getting better every day. Teacher said she was putting everything in her mouth today at the end of the day and her hair is up so I'm assuming she was putting it in her mouth also . I made a suggestion of using her sour spray when she is looking for stimulation in the mouth we'll see if they take the advice. I'm still very stressed about her feet so today I put one compression brace on and one smo to see if that would help with the left foot problem. We'll see new doc Nov 30. Well i guess that's enough venting for now.............

Hi my name is Rochelle and I am the mother of two wonderful children Logan (9) and Hannah (6). My daughter Hannah has Cerebral palsy,but that does not define her she is the happiest kid I have ever met she is always smiling. For the past 6 years we have been fighting this disability with everything we have. The doctors said she probably wouldn't progress much from infancy but she showed them. At 3and a half she started walking on her own with only the aid of her smo braces. She came home with a g-tube after birth and we had it removed two months later and have never looked back. Her biggest obstacle is eating and speech, she can only say about 7 words right now but her sounding out letters is getting better every day. We are having a problem with her foot braces waiting to get in to see new doctor at the end of Nov. Hannah is in First grade in a regular class with the help of and aid and it is getting better every day. The teachers have never had some one like her before so they are learning how to deal with her and her lack of communication.