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    Royal College of Physicians article: "Do you really believe in ME?" by Dr Nina Muirhead

    Answer to question 3 in Q&A with Chris Ponting (https://www.s4me.info/threads/science-for-me-written-q-a-with-prof-chris-ponting.4743/#post-84998): “We know that ME has a biological component (formally: the heritability of ME/CFS is not zero) as well as non-heritable biological causes so this...
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    "Answer to IBS is in the mind" - media coverage of new Chalder/Moss-Morris trial

    Front page of the Telegraph! Whoever would have guessed that a study by Prof Chalder would conclude that CBT is an effective treatment. I wonder if someone could do a study to determine whether her unhelpful beliefs can be reversed with CBT. Perhaps Prof Chalder could conduct the study...
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    Royal College of Physicians article: "Do you really believe in ME?" by Dr Nina Muirhead

    Not directly related but relevant to Dr Muirhead’s article, a Tweet from Professor Suzanne Mason MBBS, FRCS, FFAEM, MD, Professor of emergency medicine: I’ve also shared a link to Dr Muirhead’s article with her.
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    NIH: Accelerating Research on ME/CFS meeting, 4th and 5th April 2019

    I haven’t managed to listen to any of the presentations yet but I saw this quote on Twitter. I have great respect for Maureen Hanson but I’m not sure I agree with her that we know enough about ME to call it “a disease”. Although I despise the term “chronic fatigue syndrome” I’m not convinced...
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    Appeal to the FTT for information from QMUL rejected

    I wonder if you could ask another general question at Grand Rounds: “Sometimes it is preferable to divert from pre-registered outcome measures in clinical trials in order to make the results ‘more consistent with the literature, and with [the authors’] clinical experience.’ Agree or disagree?”
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    Appeal to the FTT for information from QMUL rejected

    One of the things that puzzles me is why the law should consider a campaign to be less legitimate than an individual acting alone. If the law is discouraging collaboration and encouraging people to act alone it seems likely to result in more FOI requests and therefore more disruption – the...
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    Can one smell Parkinson's disease?

    I asked Caroline from the Biobank about this the last time she came to take samples from me. She said it was something the Biobank team were looking into – in fact I think she said they had a meeting scheduled about it the next day. Do know anything more about it @Jonathan Edwards?
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    Response: Sharpe, Goldsmith and Chalder fail to restore confidence in the PACE trial findings

    As I said on the other thread, I think @Tom Kindlon and @Carolyn Wilshire ’s response is perfect. Thanks again to both of you. I’ve shared the PACE authors’ admission with Tim Hartford (BBC More or Less) and David Colquhoun on Twitter. Can anyone think of anyone else it might be worth sharing...
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    #MEAction: A response to Dr Mark Porter’s article about ME in The Times

    If someone could add a comment below the Times article with a link to my article that would be very helpful. Meanwhile...
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    #MEAction: A response to Dr Mark Porter’s article about ME in The Times

    https://www.meaction.net/2019/03/25/a-response-to-dr-mark-porters-article-about-me-in-the-times/ I actually started writing the article as a post on S4ME but as it got longer I decided to submit it as an article for #MEAction. If you feel I’ve overlooked anything I should have mentioned, or...
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    Sunday Times readers comments: "The ‘invisible illness’: what it feels like to live with chronic fatigue syndrome or ME"

    There were also 3 letters in response to Liddle’s article. There are many adjectives which come to mind when thinking about how to describe Liddle but brave is not among them.
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    MEAction: Our Community will Not Suffer Stigma and Distortion

    I understand the important point you’re making, but I think you’re being over cautious. The article doesn’t say that #MEAction is opposed to any other types of research, it just states the need for biomedical research. In fact, the article makes no comment on psychological research per se, so I...
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    MEAction: Our Community will Not Suffer Stigma and Distortion

    Remember that anyone can volunteer to join #MEAction and help to produce articles like this, as several S4ME members have. I don’t do nearly as much as many others, but I like the fact that I can chip in as and when I feel able to, without any pressure or expectation. Of course, there are...
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    CORRESPONDENCE The PACE trial of treatments for chronic fatigue syndrome: a response to WILSHIRE et al (2019) Sharpe, Goldsmith & Chalder

    And possibly Hofstadter’s Law: “It always takes longer than you expect, even when you take Hofstader’s Law into account.”
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    CORRESPONDENCE The PACE trial of treatments for chronic fatigue syndrome: a response to WILSHIRE et al (2019) Sharpe, Goldsmith & Chalder

    Not at all. I think the tone is perfect. As I’ve said before, sometimes you need to turn down the volume in order to be heard. And there are some beautifully understated lines. I particularly like the subtle references to Sharpe and colleagues’ beliefs. This is my favourite bit: I also think...
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    Special Report - Online activists are silencing us, scientists say Reuters March 2019

    Hang on, haven’t we just agreed that all illness is biological? So if ME is an illness it must surely be biological.
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    Special Report - Online activists are silencing us, scientists say Reuters March 2019

    If there is a continuum from neurological to psychiatric, I would guess that Alzheimer’s is somewhere in the middle. But I’m no expert! I think that is a very troubling statement – particularly for people with psychiatric illnesses. There is a reason why all psychiatrists are qualified medical...
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    Special Report - Online activists are silencing us, scientists say Reuters March 2019

    Jo, I wonder if you might consider writing an article – perhaps for @dave30th ‘s blog – on why you think the physical disease v mental illness argument is wrong. It’s something which gets discussed a lot on here but doesn’t seem to be heard by the wider community. I agree with most of what you...
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    Michael Sharpe on Radio 4 Today / Tom Feilden BBC (18th march 2019)

    Thanks for the transcript @Lucibee. Much appreciated. Here’s my alternative take on what MS might have said: MK: “There have been criticisms though, haven’t there, about the methodology – the Journal of Health Psychology said that the results are at best reliable [sic]...
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