The European Association of Psychosomatic Medicine (EAPM)

Some titles from the program of this year's EAPM conference in Wien earlier this month:

Sharpe: "Biopsychosocial medicine: the EAPM mission"

Panel discussion: Functional somatic disorders - a new common classification for persistent somatic symptoms

New Challenges in somatic symptom and related disorders

Treatment of functional disorders

Long COVID

Bodily Distress Syndrome

Psychoneuroimmunology

Psychodiabetology

Psycho-Oncology

Psycho--Cardiology

https://www.eapm2022.com/mainprogramme/
 
Daisymay said:
So anecdotal evidence is completely believable to these people when it comes from are a professor who can muster up a lot of media coverage and the anecdote is supportive of the BPS view BUT if the anecdotes of harm from CBT/GET of hundreds of thousands of patients ( majority female) over decades are contrary to the BPS view then they are dismissed and are of no validity, just wrong thinking?
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Nah it's only 'believeable' to them because it backs up what they want to claim. If he was to be saying the opposite not sure they'd be changing their tune on what they think of long covid and having it at their conference.

the bit I am intrigued by (wondering how long he knew these people, as he was in the loop with some linked via the circuit) is did they reply to Garner's earlier tweets disagreeing with him in the early days when he was saying 'oh no I've got ME' and if not why not?
 
Tony said:
Paul Garner has been elected as the patient study cohort, the non blind control group, the Director or faith based medicine and the tea lady. He also gets personal use of the wheelbarrow they use to roll him out in for every conference.

Someone should look into the last one, that's got to be a tax benefit of some kind.
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Ha ha - it's all a bit 'League of Gentlemen' (BBC TV show from a while back: https://en.wikipedia.org/wiki/The_League_of_Gentlemen where the same few actors played all the characters) with this group anyway
 
Just watching the first 45 seconds makes me want to throw up. Not very helpful or scientific, but, just a statement of fact from where I am sitting right now, on the sofa, wishing I was well enough that I could do military fitness, have a scuba diving holiday and that it was as simple as thinking myself better.
 
Fainbrog said:
Just watching the first 45 seconds makes me want to throw up. Not very helpful or scientific, but, just a statement of fact from where I am sitting right now, on the sofa, wishing I was well enough that I could do military fitness, have a scuba diving holiday and that it was as simple as thinking myself better.
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imagine getting to do all of those things, and no payback that means you spend most of the holiday in bed (even if mild) or it causes a relapse to an even lower level of function.

That's what is so sickening about what they put out. Many can try and do these things - but they get an unfair level of pain and health decline in return. We all find it so sad because we wish to be doing it all but now doing so would rule out chances of ever doing it in future. Where's the admiration when we manage it despite and pay the price but had our dream? or for having the self-discipline to forgo it just so we don't become more dependent?

Yet they pretend not only does that pain not exist (many are ex-athletes with that same mindset and wish - not that Garner appears to be that) but what we need is inspiring (exact OPPOSITE). I'm bored of people who didn't like PE taking up running in their 40s lording it over ME patients. Not knowing how damn good we are to be outputting what we are given if you just took out % disability it would be so much less (you realise how much norms waste their energy they are lucky to have)

Id love it if ME charities could yearly distribute as heavily as they can (ideally in the press) the workwell paper on how we are not unfit
 
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Our son, mid 30s, fit, fully vaccinated, got very poorly with Covid 19 back in March. Was extremely poorly for a couple of weeks or so, and then extremely fatigued, exhausted, ME/CFS-like for weeks and weeks after, but thankfully with a slow but steady improvement since then. Not yet back to normal, but well on the way there. Was this due to mind over matter? No, it bl****y wasn't. It was down to seriously pacing himself, with lots of advice to do that (including from his GP I'm very pleased to say), and with his work being very supportive. But of course as he improves, the pacing strategy means he can carefully do more and more.

People do get better thankfully, and if you do get better it does not mean it happened because you simply thought yourself better, even if there was a point at which your thinking switched into that mode; your thinking may well have switched in response to your body's improvement having got to such a point.
 
Kalliope said:
Some titles from the program of this year's EAPM conference in Wien earlier this month:

Sharpe: "Biopsychosocial medicine: the EAPM mission"

Panel discussion: Functional somatic disorders - a new common classification for persistent somatic symptoms

New Challenges in somatic symptom and related disorders

Treatment of functional disorders

Long COVID

Bodily Distress Syndrome

Psychoneuroimmunology

Psychodiabetology

Psycho-Oncology

Psycho--Cardiology

https://www.eapm2022.com/mainprogramme/
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Psycho-psychs
 
Moved post

Happening this week -- such a pity that it seems we don't have any allies who could be in attendance to offer some fact-checking:

MSEsperanza said:
Apologies for cross-posting from another thread:

This year's Conference of the European Association of Psychosomatic Medicine (EAPM) in June 2023 in Wrocław (Poland) will dedicate a 'symposium' to the new Guideline:

https://www.eapm-conference.org/index.php/program/main-program

FRIDAY 16 | 10:15-11:30 | KAMIENICA ROOM

SYMPOSIUM
CFS/ME: CONTROVERSY AND COMMUNICATION FOLLOWING THE 2022 UK NICE GUIDELINES

CHAIR
Per Fink.
Research Clinic for Functional disorders and Psychosomatics, Aarhus University Hospital. Denmark
  • What is CFS, the evidence for treatment and the controversy?
    Michael Sharpe    .     University of Oxford. President of the European Association of Psychosomatic Medicine (EAPM). United Kingdom.
  • Facts and myths of CFS/ME, how do we navigate, in research and in the clinic?
    Per Fink    .
    Research Clinic for Functional disorders and Psychosomatics, Aarhus University Hospital. Denmark
  • Wake me when it´s over. A personal story about a rapid recovery from CFS/ME.
    Live Landmark    .
    Department of Psychology, Faculty of Social and Educational Sciences, Norwegian University of Science and Technology. Norway
  • Debate and misinformation in the press and on social media - can we do anything about it?
    Lene Toscano    .
    Center for Functional Disorders, Region of Southern Denmark. Denmark
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