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  1. MSEsperanza

    Europe: EUROMENE

    This thread has been merged as both discuss Euromene I hesitated to open this thread, but after I had a second glance at one of the EUROMENE members' CV and an article co-authered by another member, I would like to share my readings with you. (I won't comment any further ATM - I thought this...
  2. MSEsperanza

    Hyperintense sensorimotor T1 spin echo MRI is associated with brainstem abnormality in CFS, 2018, Barnden et al

    Then, what do forum members think about Michael VanElzakker's ME research project? https://because.massgeneral.org/campaign/support-myalgic-encephalomyelitis-chronic-fatigue-syndrome-exercise-challenge-study/c168141 And, what do you think, is any of the EUROMENE groups capable of pursuing the...
  3. MSEsperanza

    Government and Insurance companies - establishing the BPS model

    Looking at the BPS approach's omnipresence with regard to sociomedical issues (especially pension scheme and rehab related, also for "organic" illnesses), and searching for any sensible application of an BPS approach in the medical world, I finally came across the WHO's BPS belief system -- it's...
  4. MSEsperanza

    Hyperintense sensorimotor T1 spin echo MRI is associated with brainstem abnormality in CFS, 2018, Barnden et al

    Thank you, @adambeyoncelowe . Sounds really interesting. But what are "EVs"?
  5. MSEsperanza

    Invisible disabilities: perceptions and barriers to reasonable accommodations in the workplace

    Have not read the (paywalled) article nor watched the video, but it would be interesting what kind of workplace adjustments were discussed. In my mild phases I probably would have benefited from two adjustments: part-time employment, and the possibility (and acceptance) of lying down during...
  6. MSEsperanza

    The MEpedia page on Myalgic Encephalomyelitis

    I agree with almost every point above, @Robert 1973 . I think we should be cautios with the term "measurable" in your last point, though: Aren't these studies based on subjective measures? And could also be interpreted as (wrong/unhelpful) "illness beliefs" or exaggerated perceptions? I think...
  7. MSEsperanza

    The MEpedia page on Myalgic Encephalomyelitis

    Unfortunately, in Germany, in most cases whether you get an "F" or a "G"-(or other "somatic") ICD-Code diagnosis is extremely relevant for doctors to assess your grade of suffering and disabilities. Actually, for any relevant medical, especially sociomedical decision, it matters whether you are...
  8. MSEsperanza

    Discussion - Does ME involve brain inflammation?

    Thank you, @Jonathan Edwards. Once again, your answers are very helpful. And once again, I am too slow to ask further, more specified questions right now. I will come back to some points maybe in related threads. Only two points for now (even though they might be more relevant for the thread...
  9. MSEsperanza

    Discussion - Does ME involve brain inflammation?

    I am particularly interested in this, so anticipated apologies in case this is going off-topic a bit. I wonder whether I understood you properly,@Jonathan Edwards: Do you think that only encephalitis deserves to be called "inflammation in the brain"? Shouldn't we distinguish between any kind...
  10. MSEsperanza

    United Kingdom: The Royal Society of Medicine

    Just realized that Sir Simon changed his presidency – from being President of the Royal College of Psychiatrists to being President of the Royal Society of Medicine. (Or was he both presidents simultanously?) The latter Royal Society perhaps was so overwhelmed by his new(?) President, that it...
  11. MSEsperanza

    Cochrane review and the PACE trial

    @Jonathan Edwards , apologies, I just realized that in this regard we already have at least one strong, very important and higly appreciated medical professor ally who came from outside the ME field. So we just need some clones of you...Any ideas how to produce them? ;)
  12. MSEsperanza

    Cochrane review and the PACE trial

    Thank you, @Jonathan Edwards. Not very encouraging, but good to know. Is this Iain Chalmers' stance in particular, and how influential is he for Cochrane in general at present? (He appears to have a very one-sided political agenda in other social areas, too, so I thought that could affect his...
  13. MSEsperanza

    Cochrane review and the PACE trial

    Do rehabilitationists in general use their imagination much to think of other forms of rehabilitation than exercise? Yet, are the authors of this review actually rehabilitationists?
  14. MSEsperanza

    Cochrane review and the PACE trial

    Just to broaden the perspective: Not only the Cochrane "Common Mental Disorders Group" but also the Cochrane "Multiple Sclerosis and Rare Diseases of the CNS Group" appears to have questionable standards of assessing research quality: Heine M, van de Port I, Rietberg MB, van Wegen EE, Kwakkel...
  15. MSEsperanza

    Germany: Restraining psychiatric patients requires court order

    I think that's right, because the Council of Europe is not identical with the Council of the EU: wikipedia: "Unlike the EU, the Council of Europe cannot make binding laws, but it does have the power to enforce select international agreements reached by European states on various topics. The...
  16. MSEsperanza

    Germany: Restraining psychiatric patients requires court order

    Germany: Restraining psychiatric patients requires court order https://www.dw.com/en/germany-restraining-psychiatric-patients-requires-court-order/a-44809053
  17. MSEsperanza

    Objective assessment of diverse types of MS related fatigue and fatiguability

    @Woolie, I thought this article might be of interest for your question posted in an related thread re: MS related fatigue: from: Rudroff, Thorsten, Kindred, John H, Ketelhut, Nathaniel B.; Fatigue in Multiple Sclerosis: Misconceptions and Future Research Directions, Frontiers in Neurology 2016...
  18. MSEsperanza

    Questionnaire on ME/CFS

    I just wonder why the questionnaire lists bacteria and fungi infections as "viral".
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