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  1. MrMagoo

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

    I suppose if you were very clever, Emeritus Professor level, you wouldn’t need to do the whole LP, you could just assimilate the information and apply it to yourself with your brilliant, insightful brain.
  2. MrMagoo

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

    Imagine being so ill after Covid, that you clock up 85 media appearances talking about it, say you meet the CCC for ME, yet you manage a holiday in the Caribbean where you contract Dengue fever, and declare yourself cured. All in 9 months.
  3. MrMagoo

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

    I know a lot of people who know him and witnessed him exercising (in public) regularly during the Summer and prior to “recovery” if Monbiot wants me to hook him up for an expose. It caused consternation.
  4. MrMagoo

    Lightning Process - discussion thread

    He’d been reading Garner’s recovery and it made sense, but he didn’t want to risk losing his stability. Then he fell victim to an “unexplained” crash so he decided to give it a go. None of that actually sounds like an unbiased account, please try harder to pretend you’re not a bot.
  5. MrMagoo

    Lightning Process - discussion thread

    Oh wow what a great guy, totally reasonable and not at all carefully crafted.
  6. MrMagoo

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

    Low public interest, unfortunately. There is a story there, but who would be bothered to.
  7. MrMagoo

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

    It’s like the philosophy experiment - if a tree falls in the forest but there’s nobody there, does it make a sound?
  8. MrMagoo

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

    Can’t believe he tagged @nice I feel embarrassed for him
  9. MrMagoo

    'Three best' questions to ask GP if they ignore you

    I’m a bit over giving GPs sympathy to be honest. The 10 min thing is rubbish, but frankly there are people in call centres dealing with angry or upset people, day in day out, who manage not to be nearly so rude and condescending as GPs have been with me. A call centre worker has never called...
  10. MrMagoo

    'Three best' questions to ask GP if they ignore you

    Yes I have met this attitude. I don’t have a consultant treating me, just speak to the GP therefore it’s not serious as there is no hospital involvement.
  11. MrMagoo

    'Three best' questions to ask GP if they ignore you

    If only there was a campaign to help doctors be less dismissive
  12. MrMagoo

    United Kingdom: ME Association news

    I was invited to join the ME Association “ME Connected” today via insta stories. I clicked the link (for research purposes of course) it took me to the Discord site but then it couldn’t complete the task as the address was invalid. So that’s working well.
  13. MrMagoo

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

    Yes the plan was to gather information which could be used as a large dataset on ME - something NICE 206 identified as a gap. Sounds good, right? Sounds like the sort of thing the ME association should fund. Except - the way this dataset would be generated was by the project group of Sarah...
  14. MrMagoo

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

    A good day to bury news… Hopefully they will be obsolete by the time they’re finished. I can dream!
  15. MrMagoo

    A Signal for Voice and Speech Abnormalities in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, 2025, Grach et al

    Funnily enough, as I have been doing exercises and silent rest over the past 8 months or so, I realised at one point that I was having more and better conversations (strength of voice-wise) however with this came the old problems I’d forgotten about - slurred words, word-finding difficulties etc...
  16. MrMagoo

    A Signal for Voice and Speech Abnormalities in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, 2025, Grach et al

    Gutted, I suffer a lot with voice issues and I’d have loved a decent piece of research. I really think it’s an overlooked symptom. When I was mild I-started to lose my voice if I got a bug. Except I didn’t get a bug, it was a little crash. It progressed until I lost my voice for over a month...
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