A personal perspective on multiple sclerosis

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  • Опубликовано: 24 ноя 2024

Комментарии • 11

  • @sushmasharma-jh1cl
    @sushmasharma-jh1cl Год назад +2

    Hi...how are you doing now....Ms is very unpredictable....God bless

  • @lilypaul8273
    @lilypaul8273 4 месяца назад

    Thanks dear...what ever may be above all ,,,there is a power and possibility to have ur normal life with God....praying....

  • @TheDAVITA28
    @TheDAVITA28 8 месяцев назад +1

    i have MS from 2018 and i am very tired. i cant stand it. how can i feel better? who can help me? i wish everyone good health ❤

  • @saanvafi6476
    @saanvafi6476 6 лет назад +7

    I was celiac for 15 yrs.whenever I ingested gluten, I had pian in gut , rashes, diarrhea .... With no problem in brain. After hep B vaccination ..... I developed confusion &. Extreme stuttering .
    I learnt hep b vaccine induces B cells ... I hope someone can come up with solution to undo what hepb vaccine did

  • @selecttravelvacations7472
    @selecttravelvacations7472 2 года назад +2

    I’ve recently had to accept that I’m no longer super woman; but I need more young, super women friends in my life! The ones I can pay for assistance, and feel like they’d do as well as I would, with the same ethics. Where are you Nashville super women? Sometimes MS IS the boss, and you just have to say, “whatever, Boss”.

  • @duyennguyenthi1604
    @duyennguyenthi1604 2 года назад

    Some segments in the video are stamped not adjacent to each other

  • @ruddyfool
    @ruddyfool 4 года назад

    Thank you for your wonderful video all the best

  • @sobiaabid625
    @sobiaabid625 7 лет назад

    is temporal arthritis also a clause of cancer?

  • @Ani3-ql4jr
    @Ani3-ql4jr 8 месяцев назад

    Unfoetunately Roche you have included this perspective - which is factually incorrect - there are many constraints and contradiction. She says ms affects her cognition but she Is knitting and she says she is. A public advocate but according to her website she is paid to be an advocate so how neutral is this comment? She also says ms patients are socially isolated but is this based on fact? This is extremely bad