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  1. NelliePledge

    UK: Dr Sarah Myhill

    Chronic fatigue :rolleyes:
  2. NelliePledge

    Effectiveness of a symptom-clinic intervention ... multiple and persistent physical symptoms, 2024, Burton, Deary et al

    Be interesting to see how they get consent from people to be involved and whether the thinking behind MUS is made explicit.
  3. NelliePledge

    Sleep trackers

    I reckon trackers can be of use if you don’t get caught up in detail. They can give you an idea of sleep patterns over a week or a month it’s a product for us Joe Bloggs not astronaut monitoring
  4. NelliePledge

    News about Long Covid including its relationship to ME/CFS 2020 to 2021

    But the problem is the pervasive influence those people have on Primary Care training and practice.
  5. NelliePledge

    PEM: Swimming compared to other activities?

    I enjoy being in water, floating, cool or warm if I try swimming it is less successful than walking despite the float effect helping take my weight. in fact I have had cramp in my calf on more than one occasion when having a little swim, which I don’t get from walking
  6. NelliePledge

    Fingernail defects?

    I’ve got vertical ridges but I’m late 50s and i assume it’s because Im getting older
  7. NelliePledge

    Importance of fatigue and its measurement in chronic liver disease - Gerber et al Jul 28 2019

    Not the first time the terminology is twisted to have surreptitious psychosomatic interpretation
  8. NelliePledge

    U.K. trial Rehabilitation exercise and psychological support after Covid 19 infection (REGAIN) Warwick University

    There’s constructive engagement and then there’s having a meeting for the sake of appearances let’s hope these researchers are just slow on further communicating and not stonewalling.
  9. NelliePledge

    George Monbiot on ME/CFS, PACE, BPS and Long Covid

    Just to say if anyone doesn’t normally do social media there are many positive comments in response to George Monbiot’s posts. but also as ever the usual mix of people who are advocating various “approaches” to ME including Lightning Process GET and so on. And the cynics and nasty people as...
  10. NelliePledge

    “it’s a medical condition … you need to support as much as possible”: a qualitative analysis of teachers’ experiences of CFS/ME, Brigden et al, 2021

    Is there a link for the paper @John Mac Based on the extract It’s positive that most of these 11 teachers were able to recognise the impact of ME on their pupils. Concluding that Clinical services should consider collaborating with teachers is hardly cutting edge thinking.
  11. NelliePledge

    The Cambridge Lectures: Demystifying ME/CFS, March 2020, deferred to January 2021 on Zoom

    This looks like a positive development. Hopefully similar local GP groups across the U.K. will also engage with the CMRC medical education group.
  12. NelliePledge

    Open Medicine Foundation (OMF)

    But in reality any conclusions we’d be attempting to draw are speculative and I’m sceptical that there’s any benefit from discussion of other people’s symptoms based on articles.
  13. NelliePledge

    Open Medicine Foundation (OMF)

    https://www.webmd.com/schizophrenia/side-effects-aripiprazole#3-7 insomnia is a very common side effect We would only be speculating on whether that is the case for Whitney.
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