The Hereditary Neuropathy Foundation presents: Charcot Marie Tooth Pt. 1
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Can anybody please direct me to part #2.
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My Dad, my three older sisters, and I all were diagnosed at birth. It made our childhoods really very hard. We all went through surgery, teasing, and jealousy of being "normal". I hate this disease, but it has opened my eyes to all the things I CAN do. My 3 year old niece now has it and must wear braces in her shoes to walk. This disease NEEDS more attention. I hope this documentary will open peoples eyes to this debilitating disease.
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Thanks for the post. We appreciate the comments. Checked out your you tube channel...Queen ROCKS!!!
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Appreciate your post and dig Queen too!
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Thankyou for this video, I can relate to everyone in it, very touching.
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ive never cried before when it came to my disease until now hearing others suffer. i have a pretty severe case but i can walk i use a crutch and people dont understand it they think its soooo weird, but my scoliosis is bad, cant use a cain. either crutch or wheelchair. but i walk barefoot i fall hard and fast , i continue to take vitamins and start an exercise program. i fully believe soma is bad for CMT... its a powerful muscle relaxer. also people said i changed in my appearence even my face.
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i have CMT also, and it is everything and more of a struggle everyday.
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I also have CMT.
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I have CMT also...
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i have CMT also. I walk on my ankle now. I have had alot of surgeries including a hip replacement. ty for posting this.
I have CMT! Thank you for posting this!
tenzime 2 years ago 19
my sister has it, i got into med school so that i could at least find a better treatment for the disease.
jamaigloo 1 year ago 11