Search results

  1. rvallee

    Evaluation of blood pressure variation in recovered COVID-19 patients at one-year follow-up: a retrospective cohort study 2024 Azami et al

    Out of curiosity, tried to find what is hypertension, the mechanism itself, and as best as I can tell... it's unknown. There is a description of what it is and risk factors but the why appears to be, dare I say, (cue spooky theremin) mysterious. Which I guess means lots of possibilities. The...
  2. rvallee

    Good Days, Bad Days Understanding the Trajectories of Technology Use During Chronic Fatigue Syndrome, 2024, Paymal and Homewood

    More like between 'bad days' and 'worse days'. I haven't had a good day in... I don't even remember. That old life is so far in the past I can't remember any of it. It's a completely different version of me, even though I am still mostly that same person. In the mildest patients good days...
  3. rvallee

    Cochrane Canada guidelines for post-COVID19 condition / Long Covid

    Two more recommendation proposed. I still don't see the point of this process, other than, hey, $9M for a low-effort report that no one will care about anyway. https://canpcc.ca/app/uploads/2024/05/can-pcc-batch-3-public-comment-english.pdf In non-hospitalized adults with post COVID-19...
  4. rvallee

    UK House of Lords/ House of Commons - relevant people and questions

    None of this really takes into account the fact that the professional associations have declared their hostile intent and refusal to implement the guidelines, and that not a single clinic, let alone care board, has actually implemented it as intended, following through on that prior declared...
  5. rvallee

    General news about Fabricated and Induced Illness syndrome (FII)

    Rare to see this acknowledgement, but it would be more accurate to say that because of the aforementioned discrimination, in severe cases, patients are abandoned and left to die slowly of starvation even though they don't have to, that it's a choice made by health care professionals. But that's...
  6. rvallee

    Examining well-being and cognitive function in people with long Covid and ME/CFS, and age-matched healthy controls, 2024, Sanal-Hayes

    It's one of the most widely reported problem, and one of the most disabling. People are literally losing the ability to read and communicate, to do basic activities of daily living, and they can't find anything at all?! Any serious scientist should be able to question their own results, that if...
  7. rvallee

    Protocol Comparing effectiveness of physiotherapy vs drug management on fatigue, physical functioning, and episodic disability for [ME] in [PCC]... 2024 Sarker

    No they don't. So the entire premise of this "study" is invalid. They are comparing ineffective things with other ineffective things, something that deserves to be mocked mercilessly. Might as well compare with potatoes for all that this matters. As in having potatoes deliver whatever...
  8. rvallee

    Review Interdisciplinary, collaborative D-A-CH consensus statement concerning the diagnostic and treatment of ME/CFS, 2024, Hoffmann et al [German]

    Looks pretty good to me. What a contrast to the clusterfuck of changing a few words and there in Australia, which really stands like a sore thumb in a recent string of guidelines and clinical recommendations like this, which actually bother to make sense of reality.
  9. rvallee

    UniteToFight2024 Long Covid and ME/CFS conference, 15th and 16th May 2024

    If you're still on xitter, it'd be good to share at least 1-2 things about the conference. It keeps on being demoralizing how few people respond, but it's leaving a record of what was known at the time, how much effort a few renegades were able to push through the indifference of the profession.
  10. rvallee

    UniteToFight2024 Long Covid and ME/CFS conference, 15th and 16th May 2024

    Actually if anyone is hesitating, no need to sign up really, it just asks for a name and email and you're good to go. Easy peasy.
  11. rvallee

    Modern environmental factors

    I'm not sure about that. ME data is unreliable, but although there is a bit of a peak in teenage years, recovery odds are higher. It's really around mid-20s that prolonged disability starts increasing. In those days, that's plenty of time to be, hell, grandparent. In the LC community I often see...
  12. rvallee

    The international ME Awareness Day, 12th May 2024

    Hard to find the right words for it, but by "the medical profession" I mean the institutions of medicine, as separate from what individuals can choose to do, usually here involving bucking what the institutions of the profession do, what they teach and acknowledge as true. As we know, MDs who...
  13. rvallee

    Opinion How to Understand the Overlap of Long COVID, Chronic Fatigue Syndrome/Myalgic Encephalomyelitis, Fibromyalgia and IBS, 2024, Goldenberg

    How so? And what does "best understood" mean anyway? Based on what? The same old crap pseudoscience built of logical fallacies that has led this to be wholly misunderstood, misinterpreted and maligned? I keep seeing this trend where MDs write stuff like "what do we now know about LC?" and...
  14. rvallee

    Engagement of mental effort in response to mental fatigue: A psychophysiological analysis 2024 Lorcery et al

    Uh, almost like there isn't some separate store of energy for movement, cognition and emotions, rather metabolic energy is metabolic energy and if you deplete reserves other forms of exertion also suffer from poorer performance. Of course there are other factors limiting this which have no...
  15. rvallee

    Poll - Have You Ever Believed In Psychosomatic Illness?

    Nope. It's not provable. It's always absence of evidence and the use of a default explanation. Used to be demons/spirits, now it's the magical mind-body thing. Same idea, really. I've seen more than enough proponents writing about this, it's always justified by not figuring out the real cause...
  16. rvallee

    The international ME Awareness Day, 12th May 2024

    Well, patients, and a few other people, have. The medical profession? Literally the problem, the blocker in the way.
  17. rvallee

    Austria: WE&ME Foundation (formerly TEMPI-Stiftung, TEMPI-Foundation)

    It would really only take one very wealthy family with the determination to solve this. That's all it would take and everything would change. But that combination is too rare.
  18. rvallee

    MIRAME Arts: short video on prejudicial views of ME/CFS

    They also collaborated with the World ME Alliance to produce this video for World ME day.
  19. rvallee

    MIRAME Arts: short video on prejudicial views of ME/CFS

    Not really sure where else to put this, but this video is really great.
Back
Top Bottom