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  1. TiredSam

    Michael Sharpe skewered by @JohntheJack on Twitter

    These tweets demonstrate that he is either a complete hypocrite, or more likely, that his lack of self-awareness is bordering on delusional. Considering the harm he has caused, it is worth recording them. They are also free entertainment, and since he has done nothing else for us, we might as...
  2. TiredSam

    Michael Sharpe skewered by @JohntheJack on Twitter

    I'm sure that anybody else, when confronted with the sight of a large blue cock, would stop whatever it was they were doing immediately, reflect upon any damage they might have caused, and resolve to do things differently in future. Only Michael Sharpe takes a picture for twitter and carries on...
  3. TiredSam

    Michael Sharpe skewered by @JohntheJack on Twitter

    Michael Sharpe now reduced to making "have you seen this big cock" tweets. He'll do anything to distract from the real story. Whatever next.
  4. TiredSam

    Name and shame list of institutions and psychiatrists/psychologists/pediatricians coercing exercise therapy on unwilling ME/CFS patients

    I completely agree with this. As someone who suffers from an unfortunate genetic predisposition to occasional lapses into sarcasm and vitriol, I have at least never kidded myself that it has ever got any results or achieved anything apart from allowing me to blow off steam and perhaps give...
  5. TiredSam

    Using the internet to cope with chronic fatigue syndrome/myalgic encephalomyelitis in adolescence: a qualitative study (Brigden et al., 2018)

    I thought seeking help online was a big no-no for ME sufferers, they should be dissuaded from googling ME and joining online support groups at all costs? Now that Crawley's pushing FITNET, suddenly we have "research" from her (9 participants, usual spin) showing that the internet is suddenly a...
  6. TiredSam

    NICE seeking committee members for Me/CFS guideline

    Looks like the prospect of Michael Sharpe's letter writing and twitter campaign must have scared them all off. Who wants to be on the receiving end of the PACE authors' vexatiousness?
  7. TiredSam

    Stockton woman reveals what it's like to live with ME (Really?)

    That's the second newpaper article on ME I've read today with no mention of "yuppie flu" and a passable (if less than perfect) description of ME uninfluenced by SMC unpleasantness. Things are looking up. EDIT: Didn't watch the video, no time.
  8. TiredSam

    BMJ: Pressure grows on Lancet to review “flawed” PACE trial

    Straws, bricks, pigs ... Can somebody say "Once upon a time there were three little ..." and have done with it?
  9. TiredSam

    Fibromyalgia: 'Like red hot lava radiating through my body'

    7-minute video on the BBC website today: https://www.bbc.co.uk/news/av/stories-45369402/fibromyalgia-like-red-hot-lava-radiating-through-my-body
  10. TiredSam

    Action for ME: The PACE trial and behavioural treatments for M.E. [position statement]

    Harrumph. "Some" is not good enough. That should be the default assumption for all people. The normal reaction to getting ME for most people is to rest until they feel better, then try to build up slowly again. It's intuitive, nobody needs to be taught that. It what works for most ailments. Most...
  11. TiredSam

    Action for ME: The PACE trial and behavioural treatments for M.E. [position statement]

    Well I was thinking of setting up a "Feel TiredSam's Arse" booth as a christmas fundraiser, but seeing as you've been so discouraging, I won't now.
  12. TiredSam

    Action for ME: The PACE trial and behavioural treatments for M.E. [position statement]

    To be fair the apology did seem sincere and SC may have had to follow legal advice on how she phrased it. Pure speculation on my part, but maybe she ran it by some people who advised her that a sincere apology containing an admission of having caused harm could make it easier for others to...
  13. TiredSam

    Action for ME: The PACE trial and behavioural treatments for M.E. [position statement]

    A positive step in the right direction. As I started reading I thought "they're not going to get everything perfect, don't be churlish now". I was even prepared to overlook "Feel" my arse. This is an extremely late apology, and for how many years now has SC been drawing 60 grand a year, and...
  14. TiredSam

    Watt from MRC defends PACE in letter to Times

    I had to look that up, not always being in touch with UK goings on. Got it now - he said "You can't polish a Trudie". I think. Brainfog.
  15. TiredSam

    Watt from MRC defends PACE in letter to Times

    Fortunately for us part of the BPS cult ideology involves believing that it's better to do something, even if it's harmful, than do nothing, so from Fiona Watt's viewpoint jumping onto the good ship PACE to drill a few more holes in the side as it goes down probably looks like a winning...
  16. TiredSam

    United Kingdom: Science Media Centre (including Fiona Fox)

    How odd - that's never made them edit anything before.
  17. TiredSam

    BMJ: Pressure grows on Lancet to review “flawed” PACE trial

    That could be the point - a million therapists on full-time contracts, training courses, "experts" being funded for further research ... exactly what they seem to be aiming for in other areas. All fits together nicely.
  18. TiredSam

    The Times - Call for review of ‘flawed’ ME research in Lancet letter

    According to experts from the Science Media Centre - oh no, sorry, nobody bothers with them any more :)
  19. TiredSam

    Invisible disabilities: perceptions and barriers to reasonable accommodations in the workplace

    Whenever I hear the phrase "in the real world" I know I'm usually going to hear someone describe the way they see things in their version of the world, complete with biases, prejudices, delusions etc. I find the phrase rather tiresome and pompous. Buggered if I'm watching any of that by the way.
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