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“Unstoppable” documentary

Discussion in 'General ME/CFS news' started by Dolphin, May 10, 2022.

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  1. tropicalmum

    tropicalmum Established Member

    Messages:
    4
    Thanks so much for the welcome. I didn't realise I placed the yoga scene on the link (oops). I get yoga isn't a cure for this illness but I personally (similar to the lady in the film) use it as a coping method to calm the body. Each to their own with what they do i guess.
     
    tropicalmum, Jun 25, 2022
    #21
    Sean, NelliePledge, DokaGirl and 3 others like this.
  2. Dolphin

    Dolphin Senior Member (Voting Rights)

    Messages:
    5,082
    The (UK) ME Association has a positive piece on this in their Autumn newsletter (p.11). Seems to be largely based on info they’ve been fed so I remain sceptical of its value.
     
    Dolphin, Oct 29, 2022
    #22
    Hutan, Peter Trewhitt and RedFox like this.
  3. Hutan

    Hutan Moderator Staff Member

    Messages:
    26,850
    Location:
    Aotearoa New Zealand
    That's a worry. Can anyone contact the MEA, @Russell Fleming? It seems that whoever is making editorial decisions there is not very aware of, well, much, about ME/CFS and the potential for uninformed people to take advantage of people newly diagnosed with ME/CFS. I mean, it's not just that the MEA isn't calling this sort of thing out, they are actively lending their credibility to it.

    Dolphin, could you perhaps put a screenshot of the article here?
     
    Last edited: Oct 29, 2022
    Hutan, Oct 29, 2022
    #23
    Peter Trewhitt, Wonko, Trish and 1 other person like this.
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