New poor Guardian article "ME and the perils of internet activism" 28th July 2019

Further to the point Frances Ryan makes in her tweet about The Observer editors, the Observer has its own twitter account @ObserverUK. People tweeting might want to use both guardian and observer tags.

Edit fixed typo in FR’s name
 
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This is a good summary of the extent of Sharpe and Wessely's bullying:



This stuff is not normal. It's abusive to the point of obsession and the purpose is entirely spiteful and intimidating.


Yes it is. This disinformation campaign by these two professors is so harmful on so many levels.

I don’t know if this is the right place to float this idea. Maybe it’s already done, maybe it’s too agressive. Here’s the plan:

I think there should be an information campaign from our side to attack this planned disinformation propaganda. A truthfull, wellinformed, scientific based story about “Professors are trolling patients to save face” but than in more suitable wording ;)

Till now a lot of their articles are getting published without source checks by the journalists. Our well intended responses won’t get as much views as the original article.
In stead of reacting, we should be pro-active. I guess the two profs are still media campaigning and sending media packages to every relevant British/ English magazine/ news station. Hoping some will pick it up to spew their view. We should do something to stop this.

If we sent our information first to news outlets, it might not be published. But that’s not the goal. When the outlets receive the disinformation from the two profs later on, it will not be the only source the journalist has. Big chance their disinformation won’t spread or there will be more balanced reporting.


These are my two cents.

I don’t know if anybody or organization did this already. I don’t know where to start, so I thought starting to float the idea here. Love to hear your two cents.

This thread is moved to the Member Only discussion over here https://www.s4me.info/threads/makin...spite-currently-pouring-from-the-media.10563/. Let’s get these ideas brewing.
 
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Yes it is. This disinformation campaign by these two professors is so harmful on so many levels.

I don’t know if this is the right place to float this idea. Maybe it’s already done, maybe it’s too agressive. Here’s the plan:
... ...
I don’t know if anybody or organization did this already. I don’t know where to start, so I thought starting to float the idea here. Love to hear your two cents.
Throw that into the Member Only discussion over here https://www.s4me.info/threads/makin...spite-currently-pouring-from-the-media.10563/. Let’s get these ideas brewing.
 
It’s amazing how the journalist was so on the side of Sharpe he allowed that opinion piece to be presented as fact and in the token “balance” bit with Dr Charles Shepherd he was presented entirely with skepticism. Note the little dig at this “silly biased dr with ME” not wanting to accept the so called wealth of psychological evidence but being convinced by the inadequate amount in the neurological field, implied because he found it more acceptable. Dr shepherd doesn’t have Cinderella slipper syndrome but the BPS lot do. I’m not sure if michael Sharpe was behind that amazing distortion of reality or the journalist by this stage was so taken with the “Sharpe & the establishment battle batty patients” story that that was a little “insightful” snark of his own. I can’t imagine any other illness where the head dr of the main patient charity, far more knowledgeable about the research field and base than Sharpe, was treated as an unreliable witness.
 
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My take - I now need to add both the excellent photos by @theJOYdecision and a link to @observer - perhaps a retweet with those added details :thumbsdown:

Stand back and wait to see.

I did also fire off an email last night (including the article) to my MP, 2 other MPs in the County who attended our #MillionsMissing event, Carol Monaghan and Darren Jones (both Science & Technology Committee) with copies to friends who are constituents of theirs (except CM).

 
My take - I now need to add both the excellent photos by @theJOYdecision and a link to @observer - perhaps a retweet with those added details :thumbsdown:
Yay that’s awesome! I made another more serious one. Didn’t know how to emphasis the humour without getting wordy so worded it for impact instead.
[EDIT] link to one place where Ron Davis criticises the psychosomatic model for ME as barbaric and malpractice. Quote is in the audio not in the written summary. https://www.rnz.co.nz/national/prog...ue-syndrome-blood-test-new-hope-for-sufferers
There might be better sources if people fine NZ source less compelling. I believe he’s used similar language in Australia?
5016F9E2-C461-4205-89A0-9502ADBEA619.jpeg
 
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Yay that’s awesome! I made another more serious one. Didn’t know how to emphasis the humour without getting wordy so worded it for impact instead.
[EDIT] link to one place where Ron Davis criticises the psychosomatic model for ME as barbaric and malpractice. Quote is in the audio not in the written summary. https://www.rnz.co.nz/national/prog...ue-syndrome-blood-test-new-hope-for-sufferers
There might be better sources if people fine NZ source less compelling. I believe he’s used similar language in Australia?
View attachment 7862

Personally, I think that use of words like 'barbaric', unless fully and clearly justified (which I think would be difficult), is likely to be counter-productive.
 
Seems Charles Shepherd really tried.



Michael Sharpe, one of the authors of the widely discredited PACE trial (https://www.meassociation.org.uk/…/me-awareness-the-pace-t…/) has expressed his thoughts on ME/CFS and internet activism in The Guardian. His comments imply that individuals with ME are discouraging researchers from pursuing work in the field.

The piece also has input from Dr Charles Shepherd, MEA Chief Medical Advisor: “He dismisses the notion of an abusive campaign as a story that has been overplayed in the media and which concerns “a tiny, tiny, tiny number of people sending emails to one of the handful of researchers in one particular area of research”.

“There are 250,000 people with this illness,” he says. “A lot of them feel very cross and angry about the way they have been treated by doctors. I mean, the numbers were probably 10 or 20 people who were accused of sending harassing or abusive emails.”

Dr Shepherd adds that, as usual, the quotes were selected by the journalist involved from a very wide ranging interview covering the history of ME/CES, research into ME/CFS, and the management of ME/CFS. Most of interview relating to significant and recent advances in biomedical research, including the the work of the ME Biobank and research into defective energy production at a cellular level, were omitted. There was also, as usual, no opportunity for Dr Shepherd to check or comment on the content or accuracy of this input before the article was printed.

The story highlights the ongoing conflict between patients with ME/CFS and those involved with the PACE trial, and clearly demonstrates the need for ongoing biomedical research into the condition. We understand that this is an emotive area for many, and demonstrates just how far we still have to go in informing the medical field and general public about the true nature of M.E.

https://www.theguardian.com/…/me-perils-internet-activism-m…

#MECFS #PWME #MEResearch #PACETrial
 
It's the UK media "silly season".

I could smell this article and predict where it would be published. It's a sad indictment of where we vulnerable, disabled patients stand with The Guardian / Observer newspaper in the UK.

https://en.wikipedia.org/wiki/Silly_season

"the Times is often violent, unfair, fallacious, inconsistent, intentionally unmeaning, even positively blundering, but it is very seldom merely silly. ... In the dead of autumn, when the second and third rate hands are on, we sink from nonsense written with a purpose to nonsense written because the writer must write either nonsense or nothing."

"To retain (and attract) subscribers, newspapers would print attention-grabbing headlines and articles to boost sales, often to do with minor moral panics or child abductions"

"In Spain the term serpiente de verano ("summer snake") is often used, not for the season, but for the news items. The term is a reference to the Loch Ness Monster and similar creatures, who are reputed to get more headlines in summer."
 
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My brief comments on some of what is said in the article:

"The trial became the subject of controversy for several reasons. One is that it looked at ways of dealing with the symptoms of an illness rather than exploring a cure for a disease. Another is that it suggested there might be a psychological component to the manner in which sufferers experience the illness.”
When researchers publish clinical trials on other behavioral interventions for ME/CFS such as the envelope theory or pacing, there is little controversy. When papers describe the negative effects stigma and misunderstanding have on ME/CFS patients there are no claims that studying this psychological component is inappropriate. When the vice-president of the IACFS/ME Lily Chu, wrote an article about depression and suicide in ME/CFS and the lack of access to appropriate mental health care, she was lauded for raising the issue. Some of the most vocal critics of the PACE trial such as James Coyne, Leonard Jason, Ellen Goudsmit and Carolyn Wilshire have been academic psychologists. It seems rather unlikely that they criticize the trial for "suggested there might be a psychological component to the manner in which sufferers experience the illness.”"

"finally, question marks were raised over the trial’s methodology."
The article doesn’t mention that the authors deviated from their protocol in reporting the outcomes and results of the PACE trial. They failed to specify these changes in full and did not provide a sensitivity analysis to see how the changes affected the results. When this was pointed out, the PACE-authors refused to provide answers or information about the effect of these changes. PLOS One had to publish an expression of concern for one of the PACE-publications because the authors’ refused to share their data is as recommended by journal policy. Eventually part of PACE trial data became available, through a freedom of information request and first tier tribunal decision. A reanalysis according to the method specified in the published protocol, found that the PACE authors had inflated recovery and improvements rate threefold. There was no longer a significant difference between the intervention groups. An open letter signed by more than 100 prominent ME/CFS experts including researchers clinicians and MP's has called the Lancet to "commission an independent re-analysis of the individual-level trial data, with appropriate sensitivity analyses."

"David Tuller, a former HIV campaigner, who has become something of a hero to the ME/CFS community in the UK."
David Tuller is an experienced journalist and Senior Fellow in Public Health in Journalism at the Center of Global Public Health, School of Public Health, University of California, Berkeley, California. Tuller reported on the findings of the PACE-trial in 2011 in an article for the New York Times, titled “Psychotherapy Eases Chronic Fatigue Syndrome, Study Finds.” It’s only when confronted with critical comments that he began to delve deeper into the methodological issues and became a vocal critic of the PACE-trial.

"he was instrumental in persuading the respected science journal Cochrane Database of Systematic Reviews to withdraw a paper that looked at eight randomised controlled studies of exercise therapy for ME/CFS."
Cochrane received a formal complaint about its review on graded exercise therapy by Robert Courtney in 2018. An internal audit at Cochrane indicated Courtney’s criticism to be well-founded. Therefore Cochrane has insisted on a revised version of the review which is currently ongoing. A detailed analysis of the review was published by Vink & Vink-Niese in 2018 in Health Psychology Open, doi: 10.1177/2055102918805187.

"Sharpe says that the Cochrane editor “wilted badly… under direct pressure” from activists. The editor has since retired, and Sharpe understands that his decision is to be reversed."
This claim has proven to be unfounded. Regarding the decision to potentially withdraw the review, former Editor in Chief David Tovey publically stated, “this not about patient pressure.” An internal email exchange between Cochrane and the Norwegian Institute of Public Health (which houses two of the authors of the review) indicates that concerns about the Cochrane review were raised by multiple experts. “When a collection of experienced and dispassionate colleagues are all making, in effect, the same criticisms”, Tovey wrote in an email, “it is hard to ignore this.” https://wordpress.com/block-editor/post/mecfsskeptic.wordpress.com/16

"He maintains that there was nothing untoward or biased about the trial. “We got a fairly clear answer, but it wasn’t an answer that people wanted to hear.”
The main researchers of the PACE have designed, studied and promoted graded exercise therapy (GET) and cognitive behavioral therapy (CBT) in ME/CFS, before the start of the PACE trial. A document by the authors explaining the need for the PACE trial, wrote: “We ourselves completed three out of seven of the RCTs of CBT and GET. The therapies and measures to be used are essentially the same as used in these successful trials.” Michael Sharpe was the lead author of “the Oxford criteria” used to diagnose patients eligible for the trial. Another author, Trudie Chalder, was the lead author of one of the trial’s primary outcome measure tools – the Chalder Fatigue Scale. The hypothesis, as specified in the trial protocol, was that GET and CBT would outperform the medical care offered in the control groups. During the study, the PACE team published a newsletter for participants that included information about the new NICE guidelines recommending GET and CBT and glowing testimonials from earlier trial subjects about how much the “therapy” and “treatment” helped them.

"He believes ME/CFS activists are absolutely set against “any implication whatsoever that there could be any aspect to their illness which isn’t rooted in biological disease. Any little hint that it couldn’t be, becomes [the] equivalent of saying it’s not real, it’s imagined, you’ve made it up.”
I hope that ME/CFS advocates are entitled to a full reply to this accusation.
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