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  1. MrMagoo

    Why don't doctors trust women? Because they don't know much about us

    That’s because you’re a man. Have you ever been advised to have a baby to resolve a medical concern? It’s not a race to the bottom, medical care is woeful but we also know it’s worse for women, and for people of colour and the disabled. There are a wealth of studies, a recent one on how women of...
  2. MrMagoo

    Why don't doctors trust women? Because they don't know much about us

    It’s the same except you get random extra advice about having a baby or losing weight
  3. MrMagoo

    Paul Garner on Long Covid and ME/CFS - BMJ articles and other media.

    People think “I can’t still be having these symptoms, I’m having a mental breakdown” I’ve spoken to medical doctors who have this and they think they’re having a nervous breakdown. They’re not, these are the symptoms of disease. Thanks Paul! Good to know people shouldn’t think it’s mental?
  4. MrMagoo

    Paul Garner on Long Covid and ME/CFS - BMJ articles and other media.

    Maybe he’s an unreliable narrator/advisor/commentator
  5. MrMagoo

    Paul Garner on Long Covid and ME/CFS - BMJ articles and other media.

    Yeah cos GPs never jump first of all to this kind of thing being psychological. If I recall correctly, Paul, when this happened in March-April 2020 people gathered online, sharing their experience of being told they should be better by now and maybe they have anxiety/depression. And then all...
  6. MrMagoo

    Why don't doctors trust women? Because they don't know much about us

    It’s institutional/structural misogyny, that’s why.
  7. MrMagoo

    UK:ME Association funds research for a new clinical assessment toolkit in NHS ME/CFS specialist services, 2023

    I think that this was somehow “sold” as an idea to fit apps and the data set thing was shoehorned in.
  8. MrMagoo

    UK:ME Association funds research for a new clinical assessment toolkit in NHS ME/CFS specialist services, 2023

    OMG The PROMs are the new CBT You have to say you’re better even if you’re not (And by that I mean the “reinforcing GET” CBT that made you agree that overdoing it was good and didn’t make you sick)
  9. MrMagoo

    UK:ME Association funds research for a new clinical assessment toolkit in NHS ME/CFS specialist services, 2023

    I think the PROM is maybe one arm of an audit, if that helps. I read somewhere about a PROM being heralded as brilliant because the patients were having hip replacements and for some reason there were two types of hip being used. PROMs data showed patients had better improvements and faster...
  10. MrMagoo

    UK:ME Association funds research for a new clinical assessment toolkit in NHS ME/CFS specialist services, 2023

    I have been seen by ME Clinics and diagnosed GP (ME/CFS) ME clinic - Psychiatrist (Fibromyalgia) Rheumatologist (ME/CFS) ME Clinic- Psychiatrist (not ME/CFS) ME Clinic -Physio, with GP attached (never met the GP) (ME/CFS) ME Clinic- GP (ME/CFS) ME Clinic- ID consultant (ME/CFS)
  11. MrMagoo

    UK:ME Association funds research for a new clinical assessment toolkit in NHS ME/CFS specialist services, 2023

    I’m not the cleverest but does this mean we are we being treated by humanities majors and not medics?
  12. MrMagoo

    UK:ME Association funds research for a new clinical assessment toolkit in NHS ME/CFS specialist services, 2023

    I would be 100% “lost my phone/sim/reading glasses” soz.
  13. MrMagoo

    UK:ME Association funds research for a new clinical assessment toolkit in NHS ME/CFS specialist services, 2023

    I think they’re worried the clinics cant be assessed as offering value, which is slightly different. They will be replaced by an app in any case.
  14. MrMagoo

    UK:ME Association funds research for a new clinical assessment toolkit in NHS ME/CFS specialist services, 2023

    Personally I think PROMS for ME are a danger full stop (even if they were 100% ethical, and say, designed by us) because we don’t know whether we would have got better or worse without their intervention. In addition, anyone newly-diagnosed will have a little “boost” from being seen and given...
  15. MrMagoo

    UK:ME Association funds research for a new clinical assessment toolkit in NHS ME/CFS specialist services, 2023

    Again, that’s off topic from the question though. In a scenario where we are (factually) today, are PROMs bad for pwME or is just this one?
  16. MrMagoo

    UK:ME Association funds research for a new clinical assessment toolkit in NHS ME/CFS specialist services, 2023

    But the fact is the NHS is using PROMS and PROMS have been created for ME/CFS. My point is still “are all ME/CFS PROMS in the NHS going to be bad, or just Tyson’s one” rather than pondering whether the current design of the NHS, clinics, clinicians etc is wrong. I think we’d all agree the...
  17. MrMagoo

    UK:ME Association funds research for a new clinical assessment toolkit in NHS ME/CFS specialist services, 2023

    Is this “PROM” measuring “treatment” per se? A patient-reported outcome presumably can be applied in diseases which result in death or further debility. I’m sure some are just measuring “management” not treatment. The situation today is there are clinics staffed by the people they are staffed...
  18. MrMagoo

    Criticisms of DecodeME in the media - and responses to the criticisms

    Are they in any way influential (beyond the usual self-referencing which that crowd does)
  19. MrMagoo

    Criticisms of DecodeME in the media - and responses to the criticisms

    Genuine question - who cares what COFFI say, apart from its members?
  20. MrMagoo

    UK:ME Association funds research for a new clinical assessment toolkit in NHS ME/CFS specialist services, 2023

    I think if you’re employed in the NHS you shouldn’t need to seek charity funding to work on a project for the NHS. I think you should just work on it as part of your NHS duties, or get an NHS secondment, or accept that the NHS don't want you to spend your working hours producing it.
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