Search results

  1. MrMagoo

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

    This isn’t really a “ u ok hun? DM me” part on the internet, but his sentence structure has gone to pot
  2. MrMagoo

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

    People who’ve had chemo vomit at the sight of a hospital? Sounds Pavlovian and not very widespread.
  3. MrMagoo

    United Kingdom: ME Association governance issues

    It’s is all a bit bizarre isn’t it? If I were working there I’d be concerned about how Neil is carrying out his role - red flags everywhere.
  4. MrMagoo

    Red Light Therapy Has Anyone Tried it?

    I had the light therapy sauna several times. This was because I got free passes, and I was advised to try the red (you select the colour from the dial/menu) it made no discernible difference although I enjoyed having a free sauna.
  5. MrMagoo

    COFFI - The international collaborative on fatigue following infection

    Is he still being silenced then? You’d think they would want to give samples of blood to show Chris Ponting, it would be fascinating to see if they have the same patterns within as MECFS patients.
  6. MrMagoo

    COFFI - The international collaborative on fatigue following infection

    Is this the big research he was going on about the other week?Please someone ask him why PEM is delayed?
  7. MrMagoo

    United Kingdom: ME Association governance issues

    When they announce this major trial next year they think we’ll all have egg on our faces.
  8. MrMagoo

    Have you limited your activity more than you needed to?

    Pubs and restaurants! Even if the loo is on the same floor it’s a long walk. IF (a big if)
  9. MrMagoo

    United Kingdom: ME Association governance issues

    I had a year or two of spontaneous recovery apropos of nothing, then started to deteriorate repeatedly until the big one I’ve never recovered from. I’m quite glad it happened when I wasn’t doing anything different that I could peg it to.
  10. MrMagoo

    Have you limited your activity more than you needed to?

    Did you rest because militant anti-recovery people hid the lightening process and GET from you, and forced you to rest?
  11. MrMagoo

    Have you limited your activity more than you needed to?

    Yes, I know this is based on what some people have said to Dave30th, but I’d want to know why they felt they had been recovered longer than they had realised? Because it’s impossible to know! Is it a “loaded” statement? As per BPS theory that “militant anti-recovery activists” have convinced...
  12. MrMagoo

    United Kingdom: ME Association governance issues

    “Only the few baying for blood” presumably
  13. MrMagoo

    Have you limited your activity more than you needed to?

    I dream of a sanatorium, I read too much of the Chalet School books as a child! A place where you go for 6 months to rest, relax, take the air and the waters, read, sleep.
  14. MrMagoo

    United Kingdom: ME Association governance issues

    Yeah WOW I know I’m just a person, but I’m a person who used to have a corporate job. I just cannot fathom the emotive/personal feelings output with the MEA (and Tyson) organisations and their reps just don’t behave like that in my world! This language about people being “silly, nonsense, baying...
  15. MrMagoo

    Have you limited your activity more than you needed to?

    If I absolutely overdo repeatedly I get horrible vertigo which stops me doing anything
  16. MrMagoo

    Have you limited your activity more than you needed to?

    A side thought. I live alone with a cat, so I am able to control my environment. We often sit is silence, I don’t have to keep the place tidy/visitor friendly every day etc. I have had some time staying with relatives and I don’t think I could live with other people. They make noise, they talk...
  17. MrMagoo

    United Kingdom: ME Association governance issues

    Good idea @Hutan, sorry to be a pest but can we have a yes/no poll on that thread as well?
  18. MrMagoo

    Long COVID brain fog linked to lung function, 2024, Fain

    Yes, my n=1 experience of sleep apnoea was terrible brain fog and noticeably poor cognition, which has been partially resolved by getting CPAP. The ME is still there, though.
Back
Top Bottom