Coping With Charcot-Marie-Tooth DiseaseThis section is a place to share stories about Coping With Charcot-Marie-Tooth Disease Below are entries of those who have already shared their stories. We hope that you find their experiences helpful to your own situation. You may also Help others by sharing your story. To quickly access health information from your website's browser, download Let’s try and help each other! My name is Jennifer. I’m 28. My Gma, Mom, Uncle, and cousins age 10 and 13 all have cmt My 10 yr old cousins ankles are turned in and her feet slap the ground like my mom’s. It’s so bad she can’t keep up with other kids or walk an amusement park. We must all be studied on an individual basis by specialists if there is ever to be better treatments or a cure! Indiana university has a cmt database as well as a hospital in Detroit. We believe if you go to one of these your medical expenses may be covered since they are studying it!! Comments
August 2007
|
|
Archives:
The submissions from our site visitors do not reflect the opinion of Healthcommunities.com, Inc. (HC). The Content of HC's sites is intended for informational and educational purposes only, and is not intended to be a substitute for professional medical advice, diagnosis, or treatment. HC does not provide medical advice. Never disregard professional medical advice or delay seeking it because of something you've read on an HC website. Always seek the advice of your physician or other qualified health care provider regarding any medical question or condition. (See also: Website Disclaimer) |

