Search results

  1. D

    Long-term use of melatonin supplements to support sleep may have negative health effects

    Grim stuff. I cannot live without sleep meds. Evidently I can't live with them either.
  2. D

    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    I have never heard of such a thing. Maybe they believe they have brain damage and assume it's a common ME/CFS feature? I wouldn't be so quick to attribute nefarious intent to fellow patients.
  3. D

    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    I don't think this credibility with patients' explanations is necessarily at the root of the problem nor peculiar to ME/CFS. I don't think it's an accuracy thing as much as it is a siloed thing compounded by arrogance. I see it in cardiologists when I attempt to explain a channelopathy''s...
  4. D

    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    I've a couple concerns about this thread. The difference between patients who spread biobabble and clinicians/researchers who spread biobabble is power. Power resides with the latter group. There is no equivalence here. The onus is squarely on clinicians and researchers. Patients are just...
  5. D

    MRC/NIHR DecodeME Showcase meeting online and in person Nov 6th

    Sure, but it's not as if there isn't precedent. AIDS activists did it at a time their illness was taboo because of its own stigma. Of course, death was the ultimate advocate and helped immensely since it was politically garish to see so many dying. But that stigma was huge at the time, and only...
  6. D

    MRC/NIHR DecodeME Showcase meeting online and in person Nov 6th

    Individual politicians are vilifying the sick regardless. At the very least, a coordinated entity from disparate communities of the sick could generate an effective response. But perhaps even better, since as you've pointed out there's years before a general election, there's time for distinct...
  7. D

    MRC/NIHR DecodeME Showcase meeting online and in person Nov 6th

    I'm not from the UK, and I apologize should this come off as naive, but could you move to legislate change? Through the vote? How large of voters' block might pwME and LC and PTLD and MS and Parkinsons, etc,, command? If they were somehow mustered together, coordinated? I often wonder about...
  8. D

    What can the science on the impact of acute infections on cognition tell us about ME/CFS?

    Sickness behavior implies an observer. It involves a third party perspective. Little wonder it was coined by a veterinarian because his patients couldn't directly communicate how they felt. He had to infer. And by virtue of the word "behavior", thanks to the BPS cult, sickness behavior is...
  9. D

    Should we initiate development of a new, short questionnaire to identify PEM (to aid diagnosis)?

    PEM shouldn't necessarily be a qualifier. It should be proof. You don't have to have it for an ME/CFS diagnosis, but getting it cements the call.
  10. D

    Should we initiate development of a new, short questionnaire to identify PEM (to aid diagnosis)?

    As an interim? Until we have a pathology-tool? Patients have to deal with more than mere diagnoses. They have to provide proof. They've employers, disability agencies, family and friends, etc, they have to demonstrate disease. Things that can help are things that can help.
  11. D

    Should we initiate development of a new, short questionnaire to identify PEM (to aid diagnosis)?

    I'm sorry if this is redundant. What if PEM is peculiar to ME/CFS as most of us have posited? What if all these new diseases that claim PEM have - at least some of them - PEM, and that they've evolved into a condition where the Decode ME genes are activated? A qualified questionnaire might be...
  12. D

    Should we initiate development of a new, short questionnaire to identify PEM (to aid diagnosis)?

    That made me chuckle. Judging by my experience with other diseases like Lyme or Babesia or ME/CFS there are usually less doctors who think those patients have a chronic disease than actually have it.
  13. D

    On fatigability and rationing as improved terminology over fatigue and pacing

    Rationing is brilliant. I am wary of any word that has fatigue in its root. Maybe try replacing with a word thats not even medical, but conveys similar feelings? Waning, ebbing, etc, something that connotes a dminishing. Sorry, just spitballing. But I fully am behind the rationing idea.
  14. D

    What can the science on the impact of acute infections on cognition tell us about ME/CFS?

    Cognitive impairment can be sustained when it occurs in pwME ( it doesn't in all pwME). Brain fog is an inadequate qualifier, btw. I can awaken with brain fog, and shake it away before I get out of bed. I cannot shed my cognitive impairment regardless of how I try. It's worse with PEM, but...
  15. D

    Who are currently the best ME/CFS researchers?

    Plenty of precedents over the last half century, many of which are contemporaries of ME/CFS. Politics. Political fingerprints once again, but somehow inadmissible.
  16. D

    Hypothesis ME/CFS as a sickness behaviour-like response to HSV-1 infection within the brain: A hypothesis, 2025, Campbell

    You won't see it much, but there's a theory of immune tolerance that might.
  17. D

    Brain Endothelial- and Epithelial-Specific Interferon Receptor Chain 1 Drives Virus-Induced Sickness Behavior and Cognitive Impairment, 2016, Blank +

    We cannot query the mice about their motivation. Fortunately, that limitation does not apply to humans. So I'd discard the entire sickness behavior model when humans are involved. Too much erudite/academic speculation regardless. We don't do shit because we feel crappy; it's a much more...
Back
Top Bottom