Here’s how to begin winning the PACE trial war

The media and medical professions are currently at war with chronically ill and disabled people. It’s a textbook example of the establishment systematically attacking people who it thinks can’t fight back, to deflect from its own disgraceful failings. But what it didn’t expect was the so-called ‘Millions Missing’. And now, it’s time to start winning this war.

Three articles. One story.

As I previously wrote, there is currently a coordinated media war against chronically ill and disabled people who live with myalgic encephalomyelitis (ME, ME/CFS, chronic fatigue syndrome). This is because of patients and supporters’ objections to PACE trial – a study which defined treatment for them.

Firstly, I wanted to put the three articles I have written about this in one place. I hope they provide some useful commentary on the issue, and give people living with ME and their advocates some much needed support.

Article one is about how the media war is being waged:

Article two is about one of the reasons why it is:

Article three is the ‘what’ – what impact PACE trial and its proponents have had, and are having, on people living with ME – some of which I rarely see discussed:

But I also wanted to give mine and Nicola’s thoughts on how we, the ME community and the people involved, move forward.

Don’t let those who would seek to destroy you, beat you:

You are already fighting a disease of catastrophic proportions. We know how hard this is. But the likes of Michael Sharpe and the media? Anything they throw at you pales in comparison to the ravaging impact of ME. You are far, far stronger than them – even if you feel you’re not.

Beware ‘false prophets’ and ‘Trojan Zebras’:

There are going to be journalists and advocates come along, writing about ME and supporting you, who are not doing it for the right reasons. Or they will be compromised and won’t really understand why. But they’ll make out that they’re being fully supportive and really understand what’s going on.

Don’t be fooled. In the same way these people and the outlets they write for are ‘controlled political opposition’, they are controlled opposition against PACE trial.

“Ye shall know them by their fruits”. They’ll probably come with a Guardian logo. But I’ll write more on this separately.

Get clued up:

The research and evidence that blows the fraudulent nature of PACE trial is out there. If you can get your head around it – great. If it’s too much, always have the links handy, maybe saved in a “favourites” folder on your browser. This means you’re ready to drop them anytime, as evidence. The more people putting this out there, the more people will know about it.

Also bear in mind: the current media war probably has a lot to do with the review of the NICE guidelines on ME. If they can solidify now the view that anyone opposed to PACE trial is a ‘abusive’, ‘militant’ ‘activist’, when it comes to the review these opinions will be null and void. Therefore, NICE will be able to keep CBT and GET as recognised treatments.

Use the “ten commandments”:

These are from a lady called Sylvia Waites (a patient of Dr Sarah Myhill’s). Me and Nic know some of them are not practical if you’re time or financially poor, but some of them are on the money:

Thou shalt not be perfect or try to be.
Thou shalt not try to be all things to all people.
Thou shalt leave things undone that ought to be done.
Thou shalt not spread thyself too thin.
Thou shalt learn to say “NO”.
Thou shalt schedule time for thyself, and for thy supporting network.
Thou shalt switch off and do nothing regularly.
Thou shalt be boring, untidy, inelegant and unattractive at times.
Thou shalt not even feel guilty.
Thou shalt not be thine own worst enemy, but thine own best friend.

You’ll be in a far better position to challenge PACE trial and its proponents.

Support each other:

Divide and conquer is a classic tactic of the ‘establishment’, which is ultimately running the show with PACE trial. You see it in every social and political movement in history. They want us to argue amongst ourselves, as it makes us easier to pick off. Don’t do it. We may have our differences. We may all be from different backgrounds. But that’s what ME is like, no? It doesn’t care how rich or poor you are. Nor does it hurt every person in the same way. It’s still the common enemy, though. So we all need to be the common ‘resistance’.

We need to organise across campaigns. Now:

As I wrote in article two, the implications of PACE trial stretch beyond ME. But moreover, chronically ill, sick and disabled people all have a common enemy: it’s the system and its gatekeepers which leave you marginalised; without the support you need; subject to abuse from others, and often at the bottom of society.

Whether it be ME, Ehlers-Danlos syndromes, MS, mental distress – if the system worked in our best interests, you wouldn’t have to be campaigning in the first place.

So, to that end, is it not time that all campaign groups, people and advocates started to co-work, across impairments and illnesses, towards a common goal? One which puts in place the building blocks for a society we all want to see?

Check out Nic’s tweeting on #Zebras and Jen Brea’s #Nightingales. Also check out Dr Emma Reinhold‘s work. These are the starting points.

Merging our experience, stories and talents would make us unstoppable. I truly believe it. And I truly believe in all of you.

You don’t let this disease beat you. So why let a bunch of arrogant medical professionals and the complicit media?

We can do this. I promise you.

Thanks for reading x

If you like my work any gifts/donations to keep it going are gratefully accepted below. Thank you.
Donate Button


The media is waging a coordinated war against chronically ill and disabled people

The UK is currently in the grip of Brexit. But amid this chaos, there is another, more sinister story brewing. It’s that of a group of chronically ill and disabled people, and the all out war against them being waged by medical professionals and the media.

This is the first of three stories. This part deals with the media. The second will deal with the ‘whys’ of the situation. The third will deal with the real-world implications for chronically ill and disabled people.

Myalgic encephalomyelitis

As I previously wrote for The Canary:

Myalgic encephalomyelitis, commonly referred to as ME, is a chronic systemic neuroimmune disease. It affects an estimated 17 million people worldwide and around 250,000 people in the UK. While symptoms vary for every person, people living with it often experience:

  • A worsening of symptoms brought on by physical activities, mental activities, or both. Often referred to as post-exertional malaise.
  • Flu-like symptoms.
  • All-over pain.
  • Sleep disturbance / problems.
  • Cognitive impairments.
  • Impairments of the body’s autonomic systems, such as nervous, digestive, and endocrine.
  • Hypersensitivity.

But ME has been fraught with controversy. For decades (and often still to this day), the medical profession has not properly recognised it. People living with ME have been disbelievedstigmatised, given incorrect treatment, or told it’s ‘all in their heads’.

To be clear, within this piece ME is referred to as that, ME/CFS or chronic fatigue syndrome.

You can read my full body of work for The Canary on ME here.

So, this is the disease currently making the headlines.

PACE trial

Also making the news is the so-called “PACE trial”. Again, as I previously wrote for The Canary, the trial:

was a study into treatment for people living with ME. Its results claim that people living with ME can improve their illnesses, and sometimes recover, by having cognitive behavioural therapy (CBT) and by using graded exercise therapy (GET).

The results of the £5m trial, part-funded by the UK Department for Work and Pensions (DWP), were originally published in the Lancet in 2011. But they have been dismissed by many medical professionals and disabled people alike as damaging and ineffective. US government agencies have either downgraded the reliability of CBT and GET or removed them as recommended treatments altogether.

In the UK, CBT and GET are still the NHS’s approved treatments under guidelines from the National Institute for Health and Care Excellence (NICE). NICE is undertaking a review of this. But this has proved controversial. Because as ME Action UK reported, among the people sitting on the review committee are a co-author of the PACE Trial and other contentious medical professionals.

You can read my full body of work for The Canary on PACE trial here.

Now, over the past few days, there has been a flurry of stories around ME. And all of them are attacking people who oppose PACE trial.

The battle begins

It began with an article on Reuters about why one of the PACE trial researchers and main authors, Professor Michael Sharpe, was quitting his work on ME. It detailed how Sharpe and others were quitting due to being:

on the receiving end of a campaign to discredit their work…

Reuters contacted a dozen professors, doctors and researchers with experience of analysing or testing potential treatments for chronic fatigue syndrome. All said they had been the target of online harassment because activists objected to their findings. Only two had definite plans to continue researching treatments.

For me, this article was the beginning of a coordinated campaign against people opposed to the PACE trial. And it is being done by industry “shills”.

Enter the Science Media Centre

If you were wondering what I mean by shill, this may help:


‘Shilling’ for who, you may ask? The science and medical industries’ PR machine, the Science Media Centre (SMC).

It claims to be:

an independent press office helping to ensure that the public have access to the best scientific evidence and expertise through the news media when science hits the headlines

But in reality, this is not the case. Because it is actually little more than a corporate industry spin doctor, promoting the views of people who really don’t have the public’s best interests at heart.

$hilling for corporates

The author of the Reuters article Kate Kelland just happens to be quite involved with the SMC. Credit to Twitter user Carol L. Binks for pointing this out to me:

Kelland has been on board with PACE trial since 2011 – as this Reuters article shows. But she also has form.

She previously was involved in some controversy, over an article she did about chemical company Monsanto’s weedkiller and its trial in the US over its links to cancer. There were rumours she obtained vital documents from Monsanto directly. But for me, it’s also likely that the SMC had a hand in this, given they have been funded by Monsanto in the past and published analysis of the trial. Two out of the three scientists it quoted were effectively supportive of Monsanto, with one declaring a conflict of interest.

Then enter the UK fracking industry, and we have a similar scenario. Kelland pushing the safety to public health of the industry via Reuters on 31 October 2013; the same day the SMC were also promoting fracking.

If you want a double whammy, here’s another article by Kelland backing Monsanto, but with a pro-genetically modified (GM) crops thrust. This time it was specifically about Monsanto’s GM corn. And then you have the SMC also caught up in scandal over its pro-GM line – allegedly to help former UK Prime Minister David Cameron.

So, firstly we are seeing a broad kickback against criticism of PACE trial. This looks to me like it’s coordinated by the SMC. But we’re also seeing an all out war being waged in support of Sharpe.

$hilling for Michael Sharpe

Both the Times and the Daily Mail have published supportive [paywall] articles about Sharpe’s ‘troll drama’.  And both papers’ parent companies have previously funded the SMC. Meanwhile the assistant editor of the Times sits on the SMC advisory committee.

In the Sunday Times, notorious columnist Rod Liddle wrote a piece [paywall] supportive of Sharpe and critical of the “ME lobby”. That’d be ‘patients’ to the rest of us. It was factually incorrect, littered with contempt and as amateurish as they come. But Liddle, like Kelland, has form, having written a supportive piece on PACE around the time it was released. He was previously editor of BBC Radio 4‘s Today programme, the BBC forcing his hand to leave in 2002. It’s unclear just why Liddle feels so strongly about PACE and Sharpe. But again, we’re back to the Sunday Times‘ parent company previously funding the SMC.

And then, as if by magic, Sharpe appeared on the Today programme on Monday 18 March:

People such as Dr Emma Reinhold noted that the interview was completely one-sided:

But as Stewart pointed out, the SMC admitted [pdf, p4] that it spoon fed (or “seeded” as it’s known in the industry) Tom Feilden, the science and environment editor for Today, a previous story. It wrote [pdf, p4] that Feilden:

won the UK Press Gazette’s first ever specialist science writing award for breaking the story the SMC gave him about the harassment and intimidation of researchers working on CFS/ME. The SMC had nominated him for the award.

Unsurprising, maybe, when you consider one former and one current senior BBC employees both sit as trustees of the SMC.

Also, the SMC included this statement [pdf, p8] in its 2017/18 accounts:

SMC Report Grab 1.png

It did the same [pdf, p7] in 2016/17, although it referred to the “select groups or individuals” as “prejudiced”.

Further to this, Ed Sykes is SMC’s senior press manager and head of mental health and neuroscience. But he was [pdf, p10] also a “non-voting member of the advisory board” of the UK CFS/M.E Research Collaborative (CMRC), a group which historically supported [pdf, p5] PACE trial’s findings. Action for ME, part of CMRC, had been criticised for it’s partial support for PACE trial’s findings, then it’s slowness to keep up with the growing concerns over the trial.

To be fair to CMRC, last year SMC left [pdf, p4] its board and ended any involvement with it. Also, the CMRC recommitted to a biomedical focus on ME. So things there look hopeful.

But still, for me, the current media and medical storm over PACE trial, Sharpe and those critical of it is coordinated. And it’s being done, in no small part, by the SMC. It has blatantly seeded stories to Reuters, the Times, the Daily Mail and the BBC using preexisting contacts and/or it’s network of connections.

For example? This is writer/broadcaster Claire Fox tweeting praise of Sharpe’s appearance on Today programme:

Claire is the sister of Fiona Fox, the SMC’s chief executive. No, really. Then look at who’s been sharing Claire’s tweet. Mark Buckingham, for example – pharmaceutical giant Bayer’s “corporate engagement lead”. Bayer of course are current funders of the SMC.

Meanwhile, Oxford Psychiatry which also retweeted Claire’s tweet has Sharpe as a “principal investigator”.

See what’s happening here, yet? There’s no need for Russian bots. The SMC has a farm of real people acting like them all to itself.

A wider agenda

But why all this fuss? All this effort? Why all this BS?

It probably seems odd that much of the mainstream medical and media community seem so defensive of a trial, whose results have effectively banned in the US.

The situation with ME has many threads to it. Not least among these, in my opinion, is the notion that it is part of a wider pandemic of chronic illnesses worldwide. I’m convinced ME has its roots in virology/immunology. I am also certain it is catastrophically under-misdiagnosed. And I’m also convinced the degradation of our bodies via soil depletion, air pollution, poor diet and more is making humans more susceptible to diseases and illnesses than ever before.

This would be an uncomfortable truth for the corporate, globalised world. As it would throw into question the entire system, and how we structure our lives as a species and as a society. It would also add fuel to the fire over our collapsing, corporate capitalist system. So, diseases like ME are far better left ‘unexplained’. And sick and disabled people left on pharmaceutical painkillers and antidepressants. All that is for another article, though.

But for this thread of the ME story, PACE has implications far beyond people living with the disease.

The second and third articles on this will be published shortly.

If you like my work any gifts/donations to keep it going are gratefully accepted below. Thank you.
Donate Button