Great to hear
@dave30th invited to speak at the CMRC conference and to read David’s positive comments in his blog (
http://www.virology.ws/2018/10/01/trial-by-error-the-cfs-me-research-collaborative-conference/). Just a bit disappointed that he didn’t mention circle jerk!
Although I share much of David’s optimism about the changes at the CMRC, I was not entirely sure what Stephen Holgate meant when he said: “we’ve stopped looking over our shoulders now... that’s done, finished... people need to sort out what needs to be sorted out but we’re looking forward...”
According to Chambers dictionary: “If you
say that someone is looking over their
shoulder, you mean that they
feel anxious all the time about what someone may do to them.”
What was SH anxious about?
What did he think was going to be done to him? By whom?
And what what does “people need to sort out what people need to sort out” mean?
Who are these people? And what do they need to do?
I appreciate the need for diplomatic language on occasions but a little less obfuscation would be welcome.
Stephen Holgate talks about the “success story of the last 5 years” but before that he suggested that the CMRC research train had been sitting at the station for 5 years with no passengers on board. That sounds more like abject failure to me.
Does SH now accept that the CMRC has made a number of mistakes which caused stress to patients and resulted in years or inertia? Will he apologise? Does he agree with David Tuller and Chris Ponting that the PACE trial is bad science? Or does he agree with Fiona Watt, CEO of the MRC? Does he agree with David that patients have been unfairly smeared? Or does he agree with Simon Wessely and Esther Crawley, who he has previously defended and praised? Does he agree Jose Montoya who believes that ME patients are owed an apology for the way we have been mistreated? Or does he agree with Peter White?
The apparent turnaround at the CMRC is both surprising and welcome but there is still one hell of a mess that needs that needs to be cleared up, and it would be nice to see its chairman getting his hands dirty. Most ME patients are not only looking over our shoulders but having to deal with the very real harms that are being done to us by the BPS crowd and the medical establishment on a daily basis.