I know the minutes for the first couple of meetings were drafted by Sharpe. It's possible he did them all, though it's not publically (sic) known. He uses 'equipoise' in his (false and misleading) COI statement.
It says on the page re CBT-GET 'It’s very important to note that there is no published research into the effectiveness of GET and/or CBT for those who are severely affected by M.E.'
FINE wasn't explicitly CBT-GET but 'home delivered pragmatic rehabilitation—a programme of gradually increasing...
My understanding is that membership of the PAG for MEGA was confidential. I do know some quit that group. Again as far as I understand, the remnants of the PAG formed the patient representatives to the CMRC. I don't know whether that's supposed to be confidential or not.
In any case the CMRC...
I presume Christine Laennac and Jane Whittaker are the patient representatives. I presume also that Jane Whittaker is the one who liked 'Developing Magic: NLP Training' (albeit in 2011) (see attached).
Isn't it time patient representatives were chosen by... patients? Shouldn't they be elected...
Obituary of ME denier in Times today. Nothing on the illness, so maybe not of great interest.
https://www.thetimes.co.uk/article/dr-thomas-stuttaford-obituary-jljgnnbrx
Here is a Dropbox link for the file Lucy has created.
https://www.dropbox.com/s/jn4fc87v9uuy8ja/Correspondence%20from%20DWP%20about%20ME%20in%202005.pdf?dl=0
Yes, that's how they came. There is a bit missing. I could go back and ask for a better copy, but it doesn't look to me as though there is anythng important missing.
Next time I get some stuff, I'll ask them if they would try to do a better job.
I have this week received these from the DWP. I've had a quick look through.
The two things that strike me are that they confirm Aylward continued on the TSC when he left the DWP, despite his myriad COIs, and a briefing from AfME which is of some interest.
I'll get more when I can. I'm not...
Great work by all involved.
Worth pointing out a couple of things in the government response: First, it doesn't specify 'biomedical', so presumably it includes all research including eg Crawley's work on 'Chronic Fatigue'. Second, the total includes spending by charities etc, so government...
I like this line:
Functional cognitive disorder (FCD) describes cognitive dysfunction in the absence of an organic cause
But of course they're not saying it's all in our minds.
And for double top: absence of evidence...
Interesting that Sharpe, who has been insisting on Twitter that he researches CFS and sees that as different from ME, is interviewed as an expert on ME claiming that GET is effective for ME.
Odd. Dropbox to the rescue. I've uploaded it here.
https://www.dropbox.com/s/qv46p29wey1tyof/Chronic%20fatigue%20syndrome%20%26%20occupational%20health.pdf?dl=0
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