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Revision as of 23:24, 20 October 2007 editJfdwolff (talk | contribs)Administrators81,547 edits rv, the discussion is closed because both MEagenda and Angela Kennedy are under a community ban - please see WP:ANI← Previous edit Revision as of 10:52, 21 October 2007 edit undoRoadcreature (talk | contribs)4,347 edits Removed now superfluous text according to WP:NPANext edit →
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'''This is a ] topic''', which may be ]. Please read the talk page and discuss substantial changes there before making them. <br>Please ''']''' from ] before piling in '''This is a ] topic''', which may be ]. Please read the talk page and discuss substantial changes there before making them. <br>Please ''']''' from ] before piling in
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'''Archive: ]''' '''Archive: ]'''


== Summary of previous discussion ==
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The value of the Gibson report was discussed at length. It was argued that this report is not a reliable source for this particular article. Information on specific cases of ] / ] was shared. It was furthermore argued, that Simon Wessely's role in a controversy regarding the classification and treatment of ME/CFS should be clarified in the article. Potentially appropriate sources were mentioned:
==Archived==
* ''David A, Wessely S, "Chronic fatigue, ME, and ICD 10", Lancet 1993:342:1247- 1248'', where the authors claim that the WHO was wrong to classify ME as a neurological disorder under G93.3, ].
I have archived the lot, since in my view ]'s input tended to shed more heat than light. I have no objection to conducting the same debates without that particular input, but several of those comments violated core policies in respect of living individuals. <b>]</b> <small>(])</small> 16:17, 20 October 2007 (UTC)
* ''Song, S, Jason, LA, "A population based study of CFS experienced in differing patient groups. An effort to replicate Vercoulen et al.'s model of CFS", Journal of Mental Health, 2005, 14, 3, 277-289'', where the authors show that the data do not support Vercoulen's model, which is based on Wessely's views:
"In part, due to the lack of a biologic marker, several theorists have proposed psychogenic approaches for understanding CFS (Wessely, Hotopf & Sharpe, 1998). For some, CFS was assumed to be a psychologically-determined problem (Manu, Lane, & Matthews, 1988). These views ultimately affected some physicians who believed that CFS was similar to ], and that CFS would eventually have a similar fate once people recognized that most patients with this disease were really suffering from a psychiatric illness. Complicating this situation was the fact that psychiatrists and physicians have also regarded fatigue as one of the least important of presenting symptoms (Lewis & Wessely, 1992). ... These biases ...." ] 10:31, 21 October 2007 (UTC)

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Archive: Talk:Simon Wessely/Archive 1

Summary of previous discussion

The value of the Gibson report was discussed at length. It was argued that this report is not a reliable source for this particular article. Information on specific cases of myalgic encephalomyelitis / chronic fatigue syndrome was shared. It was furthermore argued, that Simon Wessely's role in a controversy regarding the classification and treatment of ME/CFS should be clarified in the article. Potentially appropriate sources were mentioned:

  • David A, Wessely S, "Chronic fatigue, ME, and ICD 10", Lancet 1993:342:1247- 1248, where the authors claim that the WHO was wrong to classify ME as a neurological disorder under G93.3, post-viral fatigue syndrome.
  • Song, S, Jason, LA, "A population based study of CFS experienced in differing patient groups. An effort to replicate Vercoulen et al.'s model of CFS", Journal of Mental Health, 2005, 14, 3, 277-289, where the authors show that the data do not support Vercoulen's model, which is based on Wessely's views:

"In part, due to the lack of a biologic marker, several theorists have proposed psychogenic approaches for understanding CFS (Wessely, Hotopf & Sharpe, 1998). For some, CFS was assumed to be a psychologically-determined problem (Manu, Lane, & Matthews, 1988). These views ultimately affected some physicians who believed that CFS was similar to neurasthenia, and that CFS would eventually have a similar fate once people recognized that most patients with this disease were really suffering from a psychiatric illness. Complicating this situation was the fact that psychiatrists and physicians have also regarded fatigue as one of the least important of presenting symptoms (Lewis & Wessely, 1992). ... These biases ...." Guido den Broeder 10:31, 21 October 2007 (UTC)

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