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  1. Esther12
    Post

    The Guardian's Science Weekly podcast - 2 November 2018 - What role should the public play in science?

    Or at the very least, apologise for screwing up! As others have pointed out, many problems with the review were clearly detailed in the comments...
    Post by: Esther12, Aug 8, 2019 in forum: Psychosomatic news - ME/CFS and Long Covid
  2. Esther12
    Post

    The Guardian's Science Weekly podcast - 2 November 2018 - What role should the public play in science?

    I don't see it as a glimmer of light, particularly as it comes just after the latest article with the Guardian promoting Sharpe's bigoted view of...
    Post by: Esther12, Aug 8, 2019 in forum: Psychosomatic news - ME/CFS and Long Covid
  3. Esther12
    Post

    Assessing cellular energy dysfunction in CFS/ME using a commercially available laboratory test, 2019, Morten, Newton et al

    Myhill is dodgy. Any attempt she makes to insert herself into issues like PACE will just be harmful for advocacy efforts. It's in 'scientific...
    Post by: Esther12, Aug 7, 2019 in forum: ME/CFS research
  4. Esther12
    Post

    Management of chronic fatigue syndrome/myalgic encephalomyelitis in a pediatric population: A scoping review, 2019, Collard and Murphy

    I just did a quick search for 'lightning' to see if they chose to ignore the problems with SMILE. They did: They're using it as evidence of "the...
    Post by: Esther12, Aug 7, 2019 in forum: Psychosomatic research - ME/CFS and Long Covid
  5. Esther12
    Post

    UK: Capita seeks to reverse 'reputational damage' after death of (agoraphobia & fibro) claimant (from brain haemorrhage)

    This whole story is really grim. The UK is a bit crap.
    Post by: Esther12, Aug 7, 2019 in forum: 'Conditions related to ME/CFS' news and research
  6. Esther12
    Post

    Bristol CFS/ME clinic researching patients' problems with Chalder Fatigue Questionnaire

    Seems unlikely a qualitative study on this from Esther Crawley & co will be useful. Wonder who decided that would be a good use of resources?
    Post by: Esther12, Aug 6, 2019 in forum: Psychosomatic news - ME/CFS and Long Covid
  7. Esther12
    Thread

    Factors associated with work status in chronic fatigue syndrome (2019) S A M Stevelink, N T Fear, M Hotopf, T Chalder

    I was sure I'd seen this posted here, but now cannot see it. They say "The early involvement of occupational health practitioners is recommended...
    Thread by: Esther12, Aug 4, 2019, 43 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
  8. Esther12
    Post

    Chronic Fatigue Syndrome & Other Difficulties: Introducing a Modern Scientific Controversy to a Biology Classroom (Liang & Zaitsev, 2019)

    Doesn't work for me - do you have some institutional log in letting you access it?
    Post by: Esther12, Aug 4, 2019 in forum: ME/CFS research
  9. Esther12
    Post

    Chronic Fatigue Syndrome & Other Difficulties: Introducing a Modern Scientific Controversy to a Biology Classroom (Liang & Zaitsev, 2019)

    I'm unable to get more than the abstract... oh well.
    Post by: Esther12, Aug 3, 2019 in forum: ME/CFS research
  10. Esther12
    Post

    Chronic Fatigue Syndrome & Other Difficulties: Introducing a Modern Scientific Controversy to a Biology Classroom (Liang & Zaitsev, 2019)

    Where did you get the full text? I have a fear it will be rubbish.
    Post by: Esther12, Aug 3, 2019 in forum: ME/CFS research
  11. Esther12
    Post

    Who is Simon Wessely?

    It's not about falling for being gaslighted, it's about trying to learn from problems of the past. The cartoon doesn't play into the prejudices...
    Post by: Esther12, Aug 2, 2019 in forum: Psychosomatic news - ME/CFS and Long Covid
  12. Esther12
    Post

    Who is Simon Wessely?

    I thought your attempted paraphrasing was an unhelpful reinterpretation of his words, and I've already tried to explain why.
    Post by: Esther12, Aug 2, 2019 in forum: Psychosomatic news - ME/CFS and Long Covid
  13. Esther12
    Post

    Who is Simon Wessely?

    I read what you said and followed the discussion fine. I respondedg to your paraphrasing by saying "I think it's a bad idea to use to term...
    Post by: Esther12, Aug 2, 2019 in forum: Psychosomatic news - ME/CFS and Long Covid
  14. Esther12
    Post

    Who is Simon Wessely?

    You think it's a good idea? I think it's unethical when Wessely and co try to make patients seem worse than they are, and the same is true if...
    Post by: Esther12, Aug 2, 2019 in forum: Psychosomatic news - ME/CFS and Long Covid
  15. Esther12
    Post

    MEAction Responds to Attacks on ME Community in the Guardian and Psychology Today

    I made a brief comment on this here:...
    Post by: Esther12, Aug 2, 2019 in forum: General Advocacy Discussions
  16. Esther12
    Post

    On line ‘survey’ re UK CFS/ME specialist services

    This survey looks ridiculous. I would love it if these people no longer had any influence over my life.
    Post by: Esther12, Jul 31, 2019 in forum: General ME/CFS news
  17. Esther12
    Post

    Cognitive and behavioural responses to symptoms in adolescents with CFS: A case-control study nested within a cohort, 2019, Loades et al

    Thanks Michiel. Bit of a nothing response... presumably the Moss Moriss paper cited was just another questionnaire based one?
    Post by: Esther12, Jul 31, 2019 in forum: Psychosomatic research - ME/CFS and Long Covid
  18. Esther12
    Post

    FITNET-NHS Esther Crawley - 5th protocol out now

    So they're looking at data as it comes in, rather than waiting til the trial is completed?
    Post by: Esther12, Jul 31, 2019 in forum: Psychosomatic research - ME/CFS and Long Covid
  19. Esther12
    Post

    New poor Guardian article "ME and the perils of internet activism" 28th July 2019

    Thanks to Shepherd for trying... I hope I wasn't unfairly critical of the bits that featured him. I'm critical of everything, and did try to make...
    Post by: Esther12, Jul 30, 2019 in forum: General Advocacy Discussions
  20. Esther12
    Post

    Who is Simon Wessely?

    I think it's a bad idea to use to term 'malingering' when putting forth the views of those who have not used that term.
    Post by: Esther12, Jul 30, 2019 in forum: Psychosomatic news - ME/CFS and Long Covid
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