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Hey, my 6 year old has mild CP. For her the main thing it has affected is her walking, in that she turns her affected leg inwards. Can still run, dance, etc. and she wears a brace to help correct this, with minimal residual affect when not wearing it. I have two questions for you if I could:

  1. Did you ever have / would you ever consider surgery if there was a chance of improving your condition? Why or why not?

  2. What kind of sleeper were you as a kid and how has that changed over your life? Apparently many kids with with CP and other similar "disorders" are shit sleepers, anxious, waking often, etc. This is my girl. Was that your experience?