“Unstoppable” documentary

[tropicalmum]

A warm welcome to the forum @tropicalmum. I hope you will stick around to understand why members here had a different response to the documentary to you. The place in the clip you linked involves yoga - 'have you tried yoga?' is something of a catch phrase around here.

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.

 

[Dolphin]

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.

 

[Hutan]

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.

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?