Guest guest Posted March 16, 2006 Report Posted March 16, 2006 Hi! I was just wondering if you have any information or know of a web site that could help me.My son is thinking about taking creatine to help his muscles. I was just wondering what affect it had on people with CMT.Any and all information would be greatful. Thank-you very much. Sherry Quote
Guest guest Posted May 9, 2006 Report Posted May 9, 2006 , I participated in a research study here at WVU hospitals which was a year long study using creatine and exercise. It did help. It built up my muscles and I had less pain while using the creatine. I was on very small amounts of creatine though and some folks in the study was given a placebo.I was one of the ones who got the creatine. My children are also doing a year long exercise research study because of the fact their aren't many studies on children with CMT. My children are only doing exercises and a neat game called Dance Dance Revalution. It has helped them somewhat with pain and have really built up thier muscles. But no creatine is used. I'm not sure for myself if it was the creatine and the exercise or just the exercise that helped me. But I can tell you, once you stop the creatine, if you don't continue to exercise, then the muscle that was gained will go away and it turned flabby in my case. Kathy Quote
Guest guest Posted May 9, 2006 Report Posted May 9, 2006 Thank you Merril, I will be really careful letting them use it. How is your son with CF doing? Quote
Guest guest Posted May 9, 2006 Report Posted May 9, 2006 I have heard of great results with this. However, I also have a child with Cystic Fibrosis and I asked his dietician about Creatine and she said it was hard on the Kidneys and Liver and wouldn't let us put him on it. Merril Quote
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