Bagehot The three myths of the NHS The National Health Service is a great institution. It is also the subject of fairy tales...
I looked up the paper: https://academic.oup.com/humrep/advance-article/doi/10.1093/humrep/dey115/5040620?searchresult=1 They didn't check for...
I would put her it the better/top quartile of non-doctors that have worked in the NHS CFS-ME clinics.
I know you are just giving them the benefit of the doubt but just to point to others there were statisticians involved who have done all sorts of...
Has anyone done this? I have a lot of Facebook friends who have ME and used the Facebook search button for "BMJ review"and separately "BMJ...
I don’t recall an 8-point improvement on the CFQ being used for anything. 8 points was the threshold for improvement on SF36 PF. My only...
A published letter in the Lancet in 2011 highlighted the data wasn’t for people of working age which they responded to and accepted yet repeated...
[MEDIA]
Possibly people with fibromyalgia who go to a forum are more ill or even more likely to have ME/CFS than those with fibromyalgia on average? I’ve...
Table of Contents Abstract i List of Tables x List of Figures xiii List of Appendices xv Abbreviations xvi Publications Arising from this study...
I logged into my ethos account which anyone anywhere can get and was able to get a full copy. In general as I recall they ask for you not to share...
A retweetable tweet: [MEDIA]
I exercised 3-4 times a week (mostly in a pool supplemented with the odd bit of cycling) for most of the 4 years I was mildly affected. I would...
A possibly interesting angle to this is the BMJ now has open peer review so if the paper had been accepted, the peer review comments would have...
I think at least indirectly that the PACE and FINE trials did affect other funding e.g. MRC research strategy came out in early May 2003. Two...
If I recall correctly, he felt he was treated unfairly by mental health researchers and felt ME/CFS applications shouldn’t necessarily require...
There was a research charity called the Persistent Virus Disease Research Foundation who funded them. They re-named themselves the CFS Research...
I hope it’s good. Has the potential to be but I have a slight concern it might focus on her rehabilitation and claim it made a huge difference...
Just to say sorry to hear about all of that.
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