This sums it up for me.
My earlier comment on the thread was not shamed just fuming
I’m remembering particularly the way I was dealt with by GPs when I was trying to understand what was wrong, what illness I had, the laughing and eye rolling when I said a friend with Fibromyalgia had suggested...
I assumed not and I think the ‘researchers’ will assume that nobody will bother to check on them so won’t hold back from coming up with their own interpretations of,or excuses why they weren’t able to meet, the requirements.
Can see it coming a mile off oh the reviewers don’t want to be named or their review published because of those people with ME and their friends “maliciously” pointing out “completely inadvertent” :whistle: omissions and errors
What world do these people live in where naming a questionnaire “acceptance” of a debilitating symptom like pain or chronic fatigue seems appropriate :banghead:
Thank you @shak8 maybe the researchers don’t realise that with @dave30th connection to Virology blog website their discussions might reach a wider audience. Perhaps they wouldn’t have been flippant if they realised.
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to our use of cookies.