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  1. S

    A new research landscape emerges in America (Simon McGrath blog April 26)

    I think ME/CFS has only received credibility in the States recently, it is still way behind. This study concluded in 2016.
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    Jen Brea $100,000 crowdfund for 2018 #MEAction activities

    She is a great speaker....gosh 100,000 by June 2nd is a big ask...I wonder why such a small window? I will be very surprised if they reach that target but very much hope they do!
  3. S

    A new research landscape emerges in America (Simon McGrath blog April 26)

    God bless Simon for posting something with a positive outlook....very much needed!
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    Pharmacological activation of AMPK and glucose uptake in cultured human skeletal muscle cells from patients with ME/CFS (2018) Newton et al

    Never heard of Mark Guthridge, is he another M.E researcher? I love to hear new names on the case
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    #OMFScienceWednesday - collection of the posts

    I have no idea what that means for me as an ME patient!
  6. S

    Blog: All The Time and None At All, Jenny Spotila

    Depressing, hope ME Action and Solve can change things....
  7. S

    David Tuller's new crowdfunding campaign (April 1, 2018)

    I wonder why they aren't appearing on donor wall even as anonymous....jeez we are conditioned into expecting something to go wrong!!
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    David Tuller's new crowdfunding campaign (April 1, 2018)

    I know, I wondered the same!!!
  9. S

    David Tuller's new crowdfunding campaign (April 1, 2018)

    Feck, where did that come from!!! Brilliant!!
  10. S

    Forward ME Group – Bodily Stress Syndrome

    I can't understand any of this only that it doesn't sound like it bodes well for us. Sometimes I feel like our battle is lost. I had an occupational health appointment during the week as part of my fit for work assessment. I explained to the doctor the devastation has had on my life. I am now...
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    The ME Show

    Oh God yeah, the last thing we want are chronic fatigue I'm recovered due the Lightening process BS. If only a line could be drawn that separates ME/CFS as per ICC from Oxford criteria folk. I dont believe for one second that there are 250,000 people with true ME in the U.K. There is an...
  12. S

    The ME Show

    An interview with Simon McGrath, Chris Ponting are suggestions. Also the severe patient in Liverpool, Sophie Cooklyn, maybe her partner could speak on her behalf if she was unable to do so....Jessica Bare Taylor is another patient who featured in Unrest and is about to punlish a book 'Girl...
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    Video: Fighting for M.E. with Carol Head | April 2018

    I love Carol Head, her commitment, passion and talent are second to none. We are so lucky to have her. She comes across as a very genuine lovely lady and is a strong speaker and negotiator. She gives me hope too.
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    USA: NIH National Institutes of Health news - latest ME/CFS webinar 14 Jan 2025

    Alvin, I hope you will be on reddit so you can ask those questions..
  15. S

    USA: NIH National Institutes of Health news - latest ME/CFS webinar 14 Jan 2025

    Processes can be changed. Fact. Lost lives can't be returned.
  16. S

    Blog: So I got married, Gary Burgess

    Congrats Gary!!
  17. S

    What is Action for ME's current (March 2018) position on the PACE trial?

    Glad to see another baby step forward for us, it's one hell of a mountain
  18. S

    Ongoing ME/CFS treatment research

    Did we scare ME/CFS off? I just want to know where he as at now in terms of trialling the supplement?
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