How fatigue researchers reason away nil results and negative findings regarding CBT in CFS and QFS

There is an interesting study here looking at how the social context of bad and misleading BPS research adversely effects the well being and health of people with ME.

[added - Obvious research too, as others have pointed out, is needed to establish if CBT can be used to address the false cognitions of BPS researchers that prevents their undertaking the basic requirement of their jobs, good science. Any one want to help with an MRC grant application. I am sure it would turn out to be cost effective.]
 
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