Yes very interesting I hope it won’t be a case of whitewashing studies based on old NICE deeming them to be under improved criteria - but I would bet money there will be an attempt from some quarters to do just that
Maybe it’s not even seen as a complaint maybe it’s put down to health anxiety or catastrophising through spending too much time researching on the internet and talking to others on patient forums
I tried looking to see if there’s already a thread for this couldn’t find one but my search skills are a bit ropey please delete if there is one
http://www.bristol.ac.uk/cricbristol/research/fatigue-research/
Crawley and others at Bristol doing fMRIs on CFS and MS folks
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