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    ME/CFS and the biopsychosocial model: a review of patient harm and distress in the medical encounter - Geraghty et al. 2018

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    ME/CFS and the biopsychosocial model: a review of patient harm and distress in the medical encounter - Geraghty et al. 2018

    In case you missed it, the comment was posted on the ME Association website. You could post your comment there also.
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    ME/CFS and the biopsychosocial model: a review of patient harm and distress in the medical encounter - Geraghty et al. 2018

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    ME/CFS and the biopsychosocial model: a review of patient harm and distress in the medical encounter - Geraghty et al. 2018

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    ME/CFS and the biopsychosocial model: a review of patient harm and distress in the medical encounter - Geraghty et al. 2018

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    ME/CFS and the biopsychosocial model: a review of patient harm and distress in the medical encounter - Geraghty et al. 2018

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    16 July 2018 - Jennie Spotila blog - 'How to represent'

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    Exploring the case for truth and reconciliation in mental health services

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    Exploring the case for truth and reconciliation in mental health services

    Helen Spandler previously wrote: https://link.springer.com/article/10.1057/s41285-017-0047-0 Social Theory & Health pp 1–15 Contesting the psychiatric framing of ME/CFS Helen Spandler Meg Allen and which mentions ME/CFS.
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    Exploring the case for truth and reconciliation in mental health services

    I haven't read this myself but these are texts that were posted today:
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    Exploring the case for truth and reconciliation in mental health services

    [Oops, this probably shouldn't be in the ME/CFS section] Free full text: https://www.emeraldinsight.com/doi/full/10.1108/MHRJ-01-2017-0011
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    Rethinking the treatment of CFS — a reanalysis and evaluation of findings from a recent major trial of GET and CBT (2018) Wilshire et al.

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    CDC Posts NEW CONTENT on ME/CFS (July 12, 2018)

    The CDC have to be careful about promoting treatments that don't have evidence from clinical trials so I don't find it that surprising they might not be more specific. I don't believe there is evidence from clinical trials that this approach is safer, though theoretically it could be. Edited to...
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    CDC Posts NEW CONTENT on ME/CFS (July 12, 2018)

    Have posted here to facilitate sharing:
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    Functional Status and Well-Being in People with ME/CFS Compared with People with MS and Healthy Controls (2018) Kingdon and al.

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    Functional Status and Well-Being in People with ME/CFS Compared with People with MS and Healthy Controls (2018) Kingdon and al.

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    Functional Status and Well-Being in People with ME/CFS Compared with People with MS and Healthy Controls (2018) Kingdon and al.

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    Functional Status and Well-Being in People with ME/CFS Compared with People with MS and Healthy Controls (2018) Kingdon and al.

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    Functional Status and Well-Being in People with ME/CFS Compared with People with MS and Healthy Controls (2018) Kingdon and al.

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    Functional Status and Well-Being in People with ME/CFS Compared with People with MS and Healthy Controls (2018) Kingdon and al.

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