The Triumph of Eminence-Based Medicine - Brian Hughes

Many thanks @Kalliope , I really find that very humbling :sun:
A character trait that I find admirable, and which is so very very alien to the likes of MS, SW, EC, etc.
"Perhaps Psychologists need to turn the Psychological Theory of unhelpful beliefs upon themselves"
Absolutely. Their own unhelpful beliefs are very damaging to PwME, and probably many others.
Great, thanks. Good catch. I keep doing that. I also picked up on a stray apostrophe elsewhere... :scream:
Could almost have been the title of a Sherlock Holmes book: The Strange Case of the Stray Apostrophe.
The main thing here is that each word in that phrase is correct. Glad it makes people smile as well :innocent:
I think one of our greatest strengths is that we need simply to convince people of the truth, the whole truth, and nothing but the truth. It is what the 'other side' fear most I'm certain, because they should.
 
'Eminence based medicine' is very apt!

___

One criticism:
I think this passage:
The World Health Organisation classified ME/CFS as a neurological disease as far back as 1969. Since then, extensive research has shown that ME/CFS involves disruption of several bodily systems, including the nervous, immune, endocrine, cardiovascular, and gastrointestinal systems. Recent studies have revealed extensive cell-functioning impairment arising from irregularities in patients’ DNA.
is implying that there are a great deal of firmly established physiological findings, when there aren't many - I'm not sure there are any at all, although there may be some promising leads at this time.

I think this problem results from falling a bit into the psychological-physical dichotomy trap. Although you've set it up as psychogenic-organic. When trying to show that ME is not psychogenic, one naturally then wants to show positive 'organic'-sounding evidence.

I would keep the word 'psychogenic' since it is central to the BPS thesis, but I think the proper opposite of it is just 'not psychogenic'. ('Organic'/'Physical'/'Biological'/'Physiological' are not useful categories because they contain every disease, condition, and syndrome, unless we wish to believe in 'metaphysical illness', which we certainly shouldn't!)

The other useful dichotomy that comes to mind is 'responds to psychological intervention' vs 'doesn't respond to psychological intervention'.

So it's enough to argue against BPS by simply showing that the psychogenic etiology thesis is unsubstantiated at best, implausible, and contradicted by the results of PACE; and showing that there is no good evidence for benefit from CBT or GET regardless of what theory they stem from.

I think overstating positive physiological evidence weakens the position of advocacy. We need the standard of argument to be high to invalidate BPS BS. And it may compromise the standard of future biomedical research, which can itself contain loads of junk, and which we need to be of the highest quality possible.
 
is implying that there are a great deal of firmly established physiological findings, when there aren't many - I'm not sure there are any at all, although there may be some promising leads at this time.
It depends what you mean. We risk missing the trees by only seeing the forest. Patients under research of deep biochemistry have hundreds to thousands (possibly over 2000 but I expect some false positives) physiological findings.

What we lack is physiological abnormalities that are proven diagnostic, either for the entire patient cohort or specific subsets. This is despite the fact that there are several tests now that clearly separate patients from healthy controls at near or at 100% accuracy. What this does not give us is an understanding of the big pathophysiological picture, or evidence that the specificity is high against all diseases.

The fact that we do not have tests that show a specific problem with all patients is not the same as saying there are no tests showing problems for most patients, though there are still issues with generalisability from, for example, severe patients to milder patients.

There are possibly nine or more diagnostic tests under development now. They are all based on specific measurable physiology.
 
Many thanks. That would be fine with me. Let me know if you get to do this. In due course I want to superimpose my slides onto the video, so that viewers can better follow what I'm saying. When I get the time...... ;)
I don't have any fancy software or anything, so did the last one (the Guardian podcast) the old-fashioned way, listening and typing. Your presentation is quite a bit longer, so I came up with the idea of slowing the soundtrack down (with software I use for recording/editing music) so I could type more, and not have to keep stopping the recording and going back.

Well, it sort of worked.........I kept the pitch the same, but I did keep laughing because it sounds like either you had had quite a few beers in the bar beforehand, or you were suffering from ME.
I think I shall persevere with it though and just try to contain my laughter.

(ps I think it will be a lot more enjoyable than transcribing MS at least)

eta: it reminded me of Chris O'Dowd on the last Leg
 
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don't have any fancy software or anything, so did the last one (the Guardian podcast) the old-fashioned way, listening and typing.
Oh my god! :jawdrop:

It is also very much a British thing. [...] It is the British clinical professions whose establishments believe that ME/CFS is psychogenic, that its main dynamics are “all in the mind”.
Unfortunately, it's not just British, and I think I don't exaggerate if I say the situation in Germany (or Denmark or Sweden) is worse than in UK, because here ME doesn't get diagnosed at all. The BPS propaganda was that successful that, instead, you are diagnosed with depression, somatoform disorder or (if you're "lucky", haha) neurasthenia. Doctors here view ME as unreal, non-existent.

Personally, I believe this is linked to the kind of health system of a country. In USA, there is no "general" health insurance (even Obama care doesn't come close to what we have in UK, Germany, France etc.), it's private. The social system isn't very good, so costs remain relatively low. (US citizens, please correct me where needed.) And USA are the first to accept ME. The other countries want to reduce costs of the health system, and the BPS teaching "it's up to the individual to get healthy" is most welcome.
 
Oh my god! :jawdrop:


Unfortunately, it's not just British, and I think I don't exaggerate if I say the situation in Germany (or Denmark or Sweden) is worse than in UK, because here ME doesn't get diagnosed at all. The BPS propaganda was that successful that, instead, you are diagnosed with depression, somatoform disorder or (if you're "lucky", haha) neurasthenia. Doctors here view ME as unreal, non-existent.

Personally, I believe this is linked to the kind of health system of a country. In USA, there is no "general" health insurance (even Obama care doesn't come close to what we have in UK, Germany, France etc.), it's private. The social system isn't very good, so costs remain relatively low. (US citizens, please correct me where needed.) And USA are the first to accept ME. The other countries want to reduce costs of the health system, and the BPS teaching "it's up to the individual to get healthy" is most welcome.

i don’t think it is whether the health system is social or private as such. US people struggle with insurance companies eg Brian Vastag. And isn’t the cost of healthcare per capita in the USA significantly more than in Canada and European countries. Maybe more to do with the organisational structure and control of healthcare/professions being easier to infiltrate and dominate by a determined group.
 
I don't have any fancy software or anything, so did the last one (the Guardian podcast) the old-fashioned way, listening and typing.
Well done :) I would warmly recommend transcribe.wreally.com if you're using the "listening and typing" method, it has some super helpful functions. (They recently added auto-transcription for English and a couple of other languages, but I haven't had a chance to try it.)
 
The social system isn't very good, so costs remain relatively low.

Actually, each person in the USA pays more into socialised health care than we do in the UK and maybe Germany. The absurd thing is that most of them get nothing in return because the contribution, despite being more than here, only covers a minority of the population - poor, old, veterans etc. So the pressure to reduce the costs of socialised medicine in the USA should be greater than here.
 
Actually, each person in the USA pays more into socialised health care than we do in the UK and maybe Germany.
@NelliePledge @Jonathan Edwards, what I meant: The US health system is mostly private. Yes, people pay more; but the state doesn't. That's what counts. In contrast, the German, UK etc. health system is also financed by the state, and the state wants to reduce costs (and make possible profit maximization).

The health system counts as a service industry. As an industry, its aim must be profit maximization. That's easier if it's private. I guess in Europe they try to get there, too, but it has to be a process, or else the population won't accept it too easily. Also, in this setting you don't want chronically sick people that can't work, you want chronically sick people that work (or "disappear").
 
Unfortunately, it's not just British, and I think I don't exaggerate if I say the situation in Germany (or Denmark or Sweden) is worse than in UK, because here ME doesn't get diagnosed at all. The BPS propaganda was that successful that, instead, you are diagnosed with depression, somatoform disorder or (if you're "lucky", haha) neurasthenia. Doctors here view ME as unreal, non-existent.

Personally, I believe this is linked to the kind of health system of a country. In USA, there is no "general" health insurance (even Obama care doesn't come close to what we have in UK, Germany, France etc.), it's private. The social system isn't very good, so costs remain relatively low. (US citizens, please correct me where needed.) And USA are the first to accept ME. The other countries want to reduce costs of the health system, and the BPS teaching "it's up to the individual to get healthy" is most welcome.
Yes, I agree.

I think that it would be hard for people such as Peter White and Trudie Chalder/Simon Wessely to set up bases like they did in Barts and King's in a health system where there are co-pays where consumers pay some or all of the costs. Too many patients would have voted with their feet/money not to attend such services and other competing services would be set up. Once Peter White and Simon Wessely had such solid bases, it allowed them to have little empires with research and the like, be seen as experts, etc.

[A reminder of some of the things Peter White and the Barts service said on draft NICE guidelines:
https://meagenda.wordpress.com/2007...g-the-nice-guidelines-for-cfs-me-tom-kindlon/ Such comments would damage the reputation of a service competing for a patient's "business".]

Accepting this doesn't mean that overall, one thinks that the NHS and similar systems aren't the best system(s). To me it's like being somebody thinking a particular drug or procedure is good or the best in a particular situation, but then going on to deny it has any side-effects.
 
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Accepting this doesn't mean that overall, one thinks that the NHS and similar systems aren't the best system(s). To me it's like being somebody thinking a particular drug or procedure is good or the best in this a particular situation, but then going on to deny it has any side-effects.
I agree. No system is ideal, and one of the possible downsides of a single-payer system is that these kinds of problems can more easily become systemic and entrenched. Though I would also suggest that the imposition of de-facto privatisation of the NHS under successive governments has played a critical role in allowing these problems to emerge.

There are no doubt other factors in play as well. Such as the UK seems to be still suffering a bad hangover from the centuries old class system and the old boys' network of privilege and arse covering, and I think that plays a big role in the failure to confront and fix these kinds of problems.
 
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