oxford

  1. Sly Saint

    United Kingdom: Oxford Health NHS Foundation Trust; Oxford University Hospitals ME/CFS service

    Note: There are two services in Oxfordshire dedicated to help patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): the OUH ME/CFS Service - and the Oxford Health ME/CFS Service. Website updated Dec 2021 Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Service...
  2. MSEsperanza

    Peter White (ed.) 2005, Biopsychosocial Medicine: An integrated approach to understanding illness

    Peter White (ed.) 2005: Biopsychosocial Medicine, An integrated approach to understanding illness. Oxford University Press https://global.oup.com/academic/product/biopsychosocial-medicine-9780198530343?cc=de&lang=en&# Links to this conference and book have been posted on different threads...
  3. Sly Saint

    Oxford Textbook of Medicine (6 edn) - The psychiatric assessment of the medical patient: Sharpe et al

    Access to the complete content on Oxford Medicine Online requires a subscription or purchase. Public users are able to search the site and view the abstracts for each book and chapter without a subscription. Chapter: The psychiatric assessment of the medical patient Author(s): Jane Walker ...
  4. InfiniteRubix

    What is "Chronic Fatigue" in the Wessely School (CFS vs CF Wessely 1997, Prins 2006, White 2011)

    Hello all, I am very familiar with the ICC, CC, CDC vs Oxford criteria discussion, prevalence differences, Oxford obfuscation, etc. but I have a very specific question about what the Wessely crew mean by "CF" vs "CFS". This is not merely academic and is of consequence for important ongoing...
  5. Andy

    Oxford Autoimmune Neurology Meeting 2019 - 5th & 6th June

    https://www.ndcn.ox.ac.uk/study-with-us/continuing-professional-development/oxford-autoimmune-neurology-meeting-2019 The programme linked to on the event webpage seems to be outdated, Karl Morten has kindly sent me the version attached to this post. He will be speaking about the, currently...
  6. Andy

    Researcher Interactions Patient Representative Reports from Dr Karl Morten's collaborative group, Oxford, UK

    So, for those of you who aren't aware, I have been fortunate enough to be invited along to take part in these meetings as a patient representative. A brief overview of Dr Morten can be found here, https://www.wrh.ox.ac.uk/team/karl-morten, and his MEpedia page is...
  7. M

    Study evaluating NICE, Oxford, and Fukuda prevalence

    I think I remember reading a UK study that characterized patients by NICE, Oxford, and Fukuda and gave the prevalence of each. Does anyone remember that study and if so, could you share the study name or link? Thanks in advance
  8. Sly Saint

    CFS (PVFS, neurasthenia, ME), (2010 updated 2018) by M Sharpe, chapter in Oxford Textbook of Medicine

    Oxford Textbook of medicine (published 2010 but updated 2018): Chronic fatigue syndrome (postviral fatigue syndrome, neurasthenia, and myalgic encephalomyelitis) Chapter: Chronic fatigue syndrome (postviral fatigue syndrome, neurasthenia, and myalgic encephalomyelitis) Author(s): Michael...
  9. Dolphin

    (Oxford,UK) Recruiting: A study looking into energy status & MRS in CFS

    via https://cfsme-registry.info [2018-02-23] Energy Status and MRS
  10. Sly Saint

    Oxford criteria

    Oxford criteria - should papers using it be excluded This is a subject that has been raised a lot, so I thought it might be good to have a thread. I only recently started looking into it a bit further than the basic diagnostic criteria. see...
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