1. Sign our petition calling on Cochrane to withdraw their review of Exercise Therapy for 'CFS'.
    Dismiss Notice
  2. Guest, the 'News in Brief' for the week beginning 3rd March 2025 is here.
    Dismiss Notice
  3. Welcome! Read the Core Purpose and Values of our forum.
    Dismiss Notice

Search Results

Search Again
Page 2 of 13
  1. dangermouse
    Post

    Understanding persistent physical symptoms: Conceptual integration of psychological expectation models and predictive processing accounts, 2020, Kube

    Yes.
    Post by: dangermouse, Feb 20, 2020 in forum: Other psychosomatic news and research
  2. dangermouse
    Post

    How to explain the 'fatigue' of ME/CFS to non-sufferers - comparisons they could understand

    It's always the same for me - lower energy and weakness. When bad, add to the mix a feeling of being really sick (as in unwell, food poisoning or...
    Post by: dangermouse, Dec 24, 2019 in forum: Post-Exertional malaise and fatigue
  3. dangermouse
    Post

    How to explain the 'fatigue' of ME/CFS to non-sufferers - comparisons they could understand

    Pre ME - I had severe food poisoning whist on holiday abroad. I was so weak I had to lie on the floor at the front of the aircraft on flight home....
    Post by: dangermouse, Dec 23, 2019 in forum: Post-Exertional malaise and fatigue
  4. dangermouse
    Post

    Psychiatry Advisor: Addressing depression in ME/CFS, 2018, Cindy Lampner

    Just a point of interest as to how mood can be affected etc: A good friend recently had a bereavement, she is normally one of the happiest and...
    Post by: dangermouse, Dec 23, 2019 in forum: Psychosomatic news - ME/CFS and Long Covid
  5. dangermouse
    Post

    Psychiatry Advisor: Addressing depression in ME/CFS, 2018, Cindy Lampner

    It's difficult to explain. Especially with a fogged up mind .. but I'll try: I don't get what I understand of as clinical depression, I tend to...
    Post by: dangermouse, Dec 23, 2019 in forum: Psychosomatic news - ME/CFS and Long Covid
  6. dangermouse
    Post

    Psychiatry Advisor: Addressing depression in ME/CFS, 2018, Cindy Lampner

    This. How is it not obvious? Who are these people? It’s not rocket science is it. :mad:
    Post by: dangermouse, Dec 22, 2019 in forum: Psychosomatic news - ME/CFS and Long Covid
  7. dangermouse
    Post

    PEM is associated with greater symptom burden and psychological distress in patients ... with CFS (2019) May, Fletcher, Klimas et al.

    I’ve not read the article, what stands out to me is: We (ME patients on forum(s)) are aware of PEM being a hallmark and telltale factor of this...
    Post by: dangermouse, Dec 22, 2019 in forum: Psychosomatic research - ME/CFS and Long Covid
  8. dangermouse
    Post

    Swollen area on upper thigh

    Hi everyone, I have good news. I finally (and fortunately, as my scan results were going to be left to be reported on for another week till I...
    Post by: dangermouse, Dec 21, 2019 in forum: Pain and Inflammation
  9. dangermouse
    Post

    MEAction: "DEMYSTIFYING THE DIAGNOSTIC CRITERIA FOR ME AND RELATED DISEASE"

    Exactly this.
    Post by: dangermouse, Nov 30, 2019 in forum: Diagnostic Criteria and Naming Discussions
  10. dangermouse
    Post

    Pain in ME–what helps you and what can I do?

    There’s nothing really that takes my pain away, but the thing that helps me most is heat. Like a hot water bottle or a warm bath (if it’s...
    Post by: dangermouse, Nov 27, 2019 in forum: Post-Exertional malaise and fatigue
  11. dangermouse
    Post

    Does PEM contribute to POTS?

    I’m due to have a 24hr blood pressure monitor done (for hypotension episodes) well I’m rearranging as I’m not up to all the energy sapping...
    Post by: dangermouse, Nov 26, 2019 in forum: Orthostatic intolerance
  12. dangermouse
    Post

    'They think disability is almost worse than being dead' - fibromyalgia article on BBC website

    This really needs to change and the public be made more aware of the spectrum of complexity that makes up disability.
    Post by: dangermouse, Nov 26, 2019 in forum: Fibromyalgia and Connective Tissue Disorders
  13. dangermouse
    Post

    MEAction: "DEMYSTIFYING THE DIAGNOSTIC CRITERIA FOR ME AND RELATED DISEASE"

    This. And, I (when I have PEM or relapsed or having brain fog for whatever random reason) forget all the symptoms (of which there are many that...
    Post by: dangermouse, Nov 26, 2019 in forum: Diagnostic Criteria and Naming Discussions
  14. dangermouse
    Post

    PEM for those who are, or were, mild sufferers, how would you describe it?

    That is my experience - and especially after I had pneumonia.
    Post by: dangermouse, Nov 26, 2019 in forum: Post-Exertional malaise and fatigue
  15. dangermouse
    Post

    Gary Burgess - The ME show, and updates about Gary's health.

    @Gary Burgess I am SO sorry to hear this news. Thinking of you and wishing you all the very best with your treatment xx
    Post by: dangermouse, Nov 23, 2019 in forum: General ME/CFS news
  16. dangermouse
    Post

    Very quick survey on anti inflammatories

    I’ve done it. :)
    Post by: dangermouse, Nov 22, 2019 in forum: Other treatments
  17. dangermouse
    Post

    NICE Guidance on Thyroid Disease - Final Guidance

    Typical :banghead:
    Post by: dangermouse, Nov 20, 2019 in forum: Endocrine: Thyroid, Adrenal, Diabetes
  18. dangermouse
    Post

    Podcast: CBT for Chronic Fatigue Syndrome: Dr Lucy Maddox, Trudie Chalder

    How offensive, back to patient blaming - again. I have really wanted to be cured, still really really want to be cured .. I’ve given my all to...
    Post by: dangermouse, Nov 20, 2019 in forum: Psychosomatic news - ME/CFS and Long Covid
  19. dangermouse
    Post

    Effects of mirthful laughter on pain tolerance: A randomized controlled investigation, 2019, Lapierre et al

    Hmm, just when you thought you’d seen it all .. this is a joke, right?
    Post by: dangermouse, Nov 18, 2019 in forum: Other psychosomatic news and research
  20. dangermouse
    Post

    Still to open How to make patients who aren't engaged in the patient community aware of studies recruiting?

    Social media involving asking ie: ME Association, Carol Monaghan, @Tom Kindlon to help out. I know one person directly who has ME but avoids...
    Post by: dangermouse, Nov 16, 2019 in forum: Recruitment into current ME/CFS research studies
Showing results 21 to 40 of 242 Next >
Search Again
Page 2 of 13