Charcot-Marie-Tooth disease

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  • เผยแพร่เมื่อ 22 ก.ค. 2024
  • This video featuring people affected by Charcot-Marie-Tooth disease (CMT) and specialist neuromuscular health professionals is an introduction to the main facets of CMT and the support that is available from Muscular Dystrophy UK.

ความคิดเห็น • 21

  • @brianlawson363
    @brianlawson363 ปีที่แล้ว

    Just found out that I have CMT. THANK YOU FOR THIS GREAT VIDEO.

  • @gamergirl5231
    @gamergirl5231 6 ปีที่แล้ว

    Great video!

  • @dryoutube
    @dryoutube 3 ปีที่แล้ว +1

    Great video. CMT is a hereditary (genetic condition) that causes motor (muscle weakness) and sensory (numbness) neuropathy.

    • @PIXELSURPRISE
      @PIXELSURPRISE 9 หลายเดือนก่อน

      And severe stabbing pains in a few of us

  • @barbeebirdee2389
    @barbeebirdee2389 6 ปีที่แล้ว +2

    Read "A Piece of the World" by Christina Baker Kline, which deals with a person who probably had this condition at a time in history when no one understood it. The character in the book is a real-life person who was often a main person included in Andrew Wyeth's paintings.

  • @brittoncromersr9280
    @brittoncromersr9280 4 ปีที่แล้ว

    I got cmt can u help me wit info

  • @rebekahbrown4052
    @rebekahbrown4052 4 ปีที่แล้ว +3

    No specialist I’ve ever been to including those at the MDA clinic in the US has ever done a damn thing for me. They have made my condition worse. The doctors are horrible in the US

    • @roycemcmahon6940
      @roycemcmahon6940 4 ปีที่แล้ว +2

      No kidding the MDA clinic is a joke, I refuse to go to another Neuro Specialist as I feel they know next to nothing about this disease. My Eye Dr knows more about this disease than all the other Dr's I have seen thru the years.

    • @poonamsvideoblogs
      @poonamsvideoblogs 4 ปีที่แล้ว

      The best info and help I have ever gotten is from other people. Facebook group too.

  • @martyrmessiah3903
    @martyrmessiah3903 4 ปีที่แล้ว

    It's caused by a "manipulated" and "modified" mutation of the POLG1 gene.

  • @munster6398
    @munster6398 7 ปีที่แล้ว +2

    just told today I have it

    • @MuscularDystrophyUK
      @MuscularDystrophyUK  7 ปีที่แล้ว

      Hi there, if the is any support that we can offer with information on the condition, healthcare, or getting in touch with others than please do get in touch with our freephone helpline on 0800 652 6352.

  • @KarenNewtonCanada
    @KarenNewtonCanada 4 ปีที่แล้ว

    I can't hear the second person. Why is she whispering?

    • @daleval2182
      @daleval2182 3 ปีที่แล้ว

      It effects your lunge function, so turn up yer device, or get a hearing aid

  • @Anna-tc6rz
    @Anna-tc6rz 5 ปีที่แล้ว +1

    Tbh I kinda wish I had this reduced sensation. My feet hurt al the time. All. The. Time.