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The whole energy/fatigue paradigm, and especially 'managing' it, has been a disaster. It has completely derailed understanding and treatment.

PCS is a high subjective financial burden What does 'subjective' mean in this context? Personal?

Yes. The correct interpretation is that doctors send patients to psychiatrists, not that patients 'see' psychiatrists. Don't know about other countries, but here a patient can't just go to a psychiatrist. They have to be referred to them by another doctor (usually a GP/PCP).

Functional motor disorder often causes persistent disabling symptoms that are associated with high healthcare costs. In recent years, specialist physiotherapy, informed by an understanding of functional motor disorder, has emerged as a promising treatment, but there is an absence of evidence of...

They all do. They have a basic template including stuff like how common it is, how difficult it is, how much it costs the economy, how important the sales pitch is, blah blah blah.

Gets released at 0430 Thursday my time, and it's late Tuesday afternoon here. So two more for me.

Now vastly more complicated and voluminous due to AI, and only likely to quickly get even worse.

who do not conduct any quality controls on submissions Maybe they are just following the example of the established mainstream journals (at least in some areas)?

Exactly. This is one of those studies that will tell us something useful, maybe even important, regardless of the actual results. Strong, weak, null. They are all meaningful outcomes that will help focus future research efforts. All that matters is that it is methodologically robust. Thanks...

Interesting. :nerd:

I don't think this necessarily holds.

Functional neurological disorder (FND) presents with neurological symptoms lacking a structural correlate and is thought to result from brain network dysfunction. Despite advances in understanding its pathophysiology, several knowledge gaps exist. The main one being the mystery of how the FND...

Mental health–related visits and visits for ill-defined symptoms and signs were elevated 14 to 15 years before MS onset, followed by neurology and ophthalmology consultations (8-9 years before onset) and musculoskeletal, sensory, and nervous system visits (4-8 years before onset). Which could...

There are few things I want more in this world than a robust in vitro model for PEM. That really would be a game changer for research and for us.

There must be accountability. Letting those responsible for this grotesque catastrophe just slink away quietly into a comfortable retirement is totally unacceptable. All that will do is let it happen again to another group of innocent victims. See FND.

The whole FND project really does just get more and more dystopian and cruel, doesn't it. Their lost for power, at whatever cost, is insatiable.

Interesting. Hope they can replicate it in a much larger sample.

That would be the late Mansel Aylward.

Thank you, @Hilda Bastian, for not letting this go. Every time I start thinking the 'authorities' couldn't get any worse, there they go and prove me wrong. Again. :mad:

It is how they avoid taking any responsibility for delivering something actually useful for the patient. 'Just asking questions.'