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  1. Cheshire

    Ex-Reporter Prevails In ERISA Suit Against Prudential

    https://www.law360.com/articles/1049513/ex-reporter-prevails-in-erisa-suit-against-prudential- (I can't remember Brian's name on the forum...)
  2. Cheshire

    Re-framing GET as pacing, or vice-versa

    When you confuse psychology with dog training...
  3. Cheshire

    Esther Crawley's contribution to #MEawarenessweek

    That's weird, and I don't know if this means anything at all, but in France, there's a similar trend with autism (disclaimer: I'm not leaning to the right). Libération (a newspaper comparable to The Guardian), and L'Humanité (linked with the communist party) have been (and still are at some...
  4. Cheshire

    Esther Crawley's presentations (excluding the 2017 TEDx talk)

    Or if they do not miraculously recover after Crawley's incredible treatment.
  5. Cheshire

    NICE ME/CFS Guideline stakeholder scoping workshop, Fri 25th May 2018

    While there are no firm evidences for a mechanism, there have been many studies that tend to show that there is something abnormal happening (I'm thinking about metabolomics or exercise studies...). We don't know yet the importance of these abnormalities, the role they play, if they discriminate...
  6. Cheshire

    Michael Sharpe skewered by @JohntheJack on Twitter

    It reminds me of Trudie Chalder totaly contradicting herself on 2 points in a Guardian article: https://www.theguardian.com/society/2015/jan/14/chronic-fatigue-syndrome-patients-fear-exercise-hinder-treatment-study-me So - a phobia in which you have to prevent patients from doing the dreaded...
  7. Cheshire

    NICE ME/CFS Guideline stakeholder scoping workshop, Fri 25th May 2018

    There's still symptoms relief (pain an sleep mainly).
  8. Cheshire

    Clare Gerada: influence on UK medical practice and ME/CFS management

    Oh my, she's not even pretending to be impartial. In line with her previous gross anti-patient stance here: https://www.s4me.info/threads/clare-gerada-patients-need-to-be-more-accountable-for-their-health-suggests-gp-mental-health-lead.1489/#post-26213
  9. Cheshire

    Publications that show ME is biological

    I don't think the PACE trial failure in itself disproves the theory of a psychological cause for ME. There are other theories not tested in the PACE trial. This failure doesn't even disprove the false illness belief hypothesis (but it certainly casts a serious doubt on its validity). It just...
  10. Cheshire

    Rethinking the treatment of CFS — a reanalysis and evaluation of findings from a recent major trial of GET and CBT (2018) Wilshire et al.

    Sorry, long (and a bit personal) post. In the early days, when I was still in limbo (am I out now? Wondering), I was told by my GP that my neurological symptoms were functional, which was not really a firm diagnosis but a track which I followed up to Stone and al. (nearly nothing on the subject...
  11. Cheshire

    Janet Dafoe - The Whitney Plea

    I just came across a few videos on twitter, and they made me feel really uneasy. First, it is difficult to understand. Then, the "pray/please" gesture for me is more a begging sign. I don't like it at all, I'm not begging for help, I'm asking governments to do their duty into financing a major...
  12. Cheshire

    Esther Crawley's contribution to #MEawarenessweek

    Not a joke... :( What a bitter hijack... Direct link: https://www.nihr.ac.uk/blogs/worries-that-keep-you-awake-at-night/8466 Just a little extract to let you have a taste of her revolting prose (this woman really has no decency): Leaving the field would be your best contribution, Esther...
  13. Cheshire

    Effects of unsupportive social interactions, stigma, and symptoms on patients with myalgic encephalomyelitis and cfs, McManimen et al, 2018

    I haven't read it all yet, but very interesting so far. THAT is the kind of psychosocial research we need!
  14. Cheshire

    A unifying theory for cognitive abnormalities in functional neurological disorders, Fibromyalgia and CFS (2018), Mark J Edwards et al.

    I agree the message is quite clear, but they do not write "cfs is psychogenic" in full letters (they do not hesitate to do it for FND though).
  15. Cheshire

    A unifying theory for cognitive abnormalities in functional neurological disorders, Fibromyalgia and CFS (2018), Mark J Edwards et al.

    Oh no, they never say it but the subtext is so clear it's as if they were screaming "all in your head". The fact they won't admit what they think but keep implying it loud (and jump on any patient that dare say it) is just really pervert. Lying to patients raises many ethical questions, but...
  16. Cheshire

    Updates from the UK ME/CFS Biobank / CureME team

    Even bigger picture here: https://i.imgur.com/Aenjq0E.jpg
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