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  1. MrMagoo

    The Born Free Protocol

    I personally was excited to have one treatment to cure my hEDS, FMS, Audhd and ME/CFS. I’m long sighted too. /sarcasm
  2. MrMagoo

    The Born Free Protocol

    I mean, the article quoted concludes that they are a hoax, really. https://www.dailymail.co.uk/sciencetech/article-14346729/Scientists-studying-alien-mummies-Peru-new-details-emerge.html Imagine having to use the Daily Mail to prove a scientific point, though.
  3. MrMagoo

    The Born Free Protocol

    The point being for every person who claims they found the cure, these are some of the most famous/recent ones
  4. MrMagoo

    The Born Free Protocol

    Yeah, for every Paul Garner/Miranda Hart/Whitney Dafoe there are a hundred of us where it didn’t work, or made thinks worse. Go fund yourself a scientific study if it’s so brilliant.
  5. MrMagoo

    Whitney Dafoe Updates

    I’m so sorry. I struggled with speaking a lot for a few years, I could only whisper, and it still disappears at the end of each day for me. It’s not given enough attention as a symptom.
  6. MrMagoo

    United Kingdom: ME Association governance issues

    Yes, it is a meme, I used it to create mine!
  7. MrMagoo

    United Kingdom: ME Association governance issues

    Shame. Maybe he has changed? I like that he states there’s no treatment or even agreed management of ME though. I wish he’d tell BACME.
  8. MrMagoo

    United Kingdom: ME Association governance issues

    Of course, that’s what all this is: they can’t admit they don’t know and there aren’t any answers.
  9. MrMagoo

    Reddit - Interesting posts on Reddit, including what some doctors say about ME/CFS

    I really don’t know. We don’t get tested for viruses like chest infections or flu. It was flu-like, sweating, sore throat, cough, fatigue but never really very serious, just a bad cold, a bug, maybe a day off work, maybe skip the gym that week. I also developed hay fever and eczema during this...
  10. MrMagoo

    Reddit - Interesting posts on Reddit, including what some doctors say about ME/CFS

    The “caught a virus but didn’t get better” is really common and repeated everywhere. I certainly would have agreed. But actually, I’d been getting “a virus” every other month for some time, and it was many years before I was introduced to the idea that for pwME maybe things were going wrong...
  11. MrMagoo

    United Kingdom: ME Association governance issues

    I made this meme and wasn’t sure where to put it It’s a hand sinking in the sea and the ME clinic reaches out, high 5s and says “just pace” and the hand sinks.
  12. MrMagoo

    United Kingdom: ME Association governance issues

    Yeah but that’s got to be spelled out and written down, basic care isn’t working right now so it needs to be specified. Deaf people aren’t given translators or even a piece of paper with writing explaining things, palliative patients are shoved in noisy corridors for days…
  13. MrMagoo

    United Kingdom: ME Association governance issues

    We are saying the same thing - we need safe care. With a broken leg there is a op, a cast off then build up gently. With cancer there’s treatments, then build up, with MS there’s a relapse, then build up. With us we just…are. So we now need to build up…A crash isn’t seen as a massive warning...
  14. MrMagoo

    United Kingdom: ME Association governance issues

    Everything NHS thesedays is a pathway, a format, a checklist. All we need are decent pathways/checklist things because there’s no real “thought”.
  15. MrMagoo

    United Kingdom: ME Association governance issues

    I think that thees an issue with the different experiences people have with different disciplines. And this goes to the heart of the problem. I’ve had terrible experiences with physios and psychiatrists, so I would probably now write them off. However if I’d been seen by, say, a Physios For ME...
  16. MrMagoo

    Reddit - Interesting posts on Reddit, including what some doctors say about ME/CFS

    Thank you. I was trying to share info back then and quite a few times it was not well received and I was told to pipe down! It was strange to see it play out. The rush to be vegan, take antihistamines, keto diets, supplements…people declaring it had made such a difference, a few weeks later...
  17. MrMagoo

    Would you say that you suffer from debilitating fatigue or extreme fatigue?

    Many things thesedays are described on a “spectrum” for example Autistic Spectrum. The idea of levels of ME severity or an ME spectrum is totally missing in most public discussion. In addition, the progress or deterioration of ME isn’t really discussed because they will always cite there are no...
  18. MrMagoo

    Reddit - Interesting posts on Reddit, including what some doctors say about ME/CFS

    But also the information is relatively new. Many people have had ME for a long time. I had GET and CBT before I had a Facebook profile. NICE guidance release in 2022 - only three years ago. Educated middle class people have no reason to doubt their doctor! I have had this conversation with so...
  19. MrMagoo

    Reddit - Interesting posts on Reddit, including what some doctors say about ME/CFS

    Now, people believe “ME is real” but also they suspect your problem isn’t really ME. They are always suspicious that you are actually depressed or attention-seeking. You never have the right sort of ME. If you are in bed, severe etc then it’s “too serious” to be ME or you’re just depressed. If...
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