Multifocal Motor Neuropathy (MMN) - Phyllis's Story

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  • เผยแพร่เมื่อ 26 ก.ค. 2024
  • To learn more about MMN, GBS and CIDP, please go to:
    www.gbscidp.ca/
    / gbs_cidpfoundationofca...
    / gbscidpcanada
    #mmn
    #multifocalmotorneuropathy
    #cidp
    #mmnawareness
    #livingwithmmn
    #mmnsupport
    #mmnadvocate
    #patientadvocacy
    #plasmapheresis
    #mmnwarrior
    #gbs
    #invisibleillness
    #autoimmunedisease
    #chronicillness
    #IVIG
    #ivigtherapy
    #gbscidpfoundation
    #gbscidpawareness
    #peripheralneuropathy

ความคิดเห็น • 17

  • @tkqbb
    @tkqbb 3 ปีที่แล้ว +6

    Thank you for sharing story. I was diagnosed MMN 5 years ago. Since MMN is rare also in japan, this is the first time see someone have circumstances.

  • @dalenesbitt
    @dalenesbitt ปีที่แล้ว

    Your description of MMN is exactly the same as what is happening to my left leg. No pain, incredibly slow atrophy.

  • @kevinbaxter7390
    @kevinbaxter7390 3 ปีที่แล้ว +2

    Each individual will be different. Meself nearly 5yrs with GBS, recently aswell diagnosed MMNCB. Unfortunately my nerves have demylinated to far. Yes had ivig but temporarily ease symptoms. So balance issues, essential tremor in both hands, two crutches, climb the stairs like a two Yr old. Am 55 male it's totally destroyed me physically mentally socially financially. I battle my own rehab daily. Get all the information you need don't get pushed away by doctors and Neurologists. From working playing Rugby cycling gym it's hell. Best wishes for all suffering

    • @desirousdreamer3983
      @desirousdreamer3983 2 ปีที่แล้ว +3

      How are you now...brother may God help u out....

    • @MrSuperMint
      @MrSuperMint ปีที่แล้ว +2

      i feel your pain. i am also 56, slowly deteriorating - trying everything i can no

  • @dannylkent1170
    @dannylkent1170 11 หลายเดือนก่อน +1

    I have had MMN for 10 years now I am 36 and it took me 7 years to get a proper diagnosis and treatments don't work. It's extremely challenging and wish all of you struggling with this horrible disease the very best 🙏

  • @DavidSamuel7
    @DavidSamuel7 7 หลายเดือนก่อน

    ❤God blessings 🙌 🙏 ✨️ ❤️

  • @vincentkoech555
    @vincentkoech555 ปีที่แล้ว

    Thankyou so much

  • @dalenesbitt
    @dalenesbitt ปีที่แล้ว +1

    Do you have problems falling asleep because of muscle twitches?

  • @ourcollectiveinsanity
    @ourcollectiveinsanity 4 ปีที่แล้ว +1

    why not rituximab?

  • @rebeccamike7770
    @rebeccamike7770 4 ปีที่แล้ว +1

    So no treatment helped you?

  • @jenniferjarreau1214
    @jenniferjarreau1214 ปีที่แล้ว

    P

  • @loriclark505
    @loriclark505 2 ปีที่แล้ว

    This is not helpful

    • @alipgreene
      @alipgreene 2 ปีที่แล้ว +6

      I think it's very helpful to hear a patient's journey. It can make you feel heard and represented, and it's interesting to hear the onset of her symptoms and how she's dealing with her illness right now.

    • @Yinyanchant
      @Yinyanchant ปีที่แล้ว +3

      We’re you expecting her to give you a cure? It was helpful for us.