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From the press release:

There's this open access paper that seems to be about the set-up of the study: Cohort description: The Danish study of Functional Disorders, 2017, Dantoft et al Abstract: The Danish study of Functional Disorders (DanFunD) cohort was initiated to outline the epidemiology of functional somatic...

Also at the link is a terrific response about the application of GRADE by NICE in the ME/CFS Guideline by @Michiel Tack (dated March 2021). If I'd read it before, I'd forgotten it. Definitely worth a read.

The forum thread on that recent study is here: Acute Corticotropin-Releasing Factor Receptor Type 2 Agonism Result in Sustained Improvement in ME/CFS - Pereira, Bateman et al, 2021

It's disappointing that everyone has fought so hard to try to remove unevidenced ME/CFS treatments only to have the MEA actively promoting another one. The evidence for TENS is extremely weak. Why would Dr Shepherd allow this? e.g. Pain Science But we have Dr Peter Gladwell in this...

I've submitted a complaint using the website's facility, noting the requirements set out in the NICE ME/CFS Guideline about any recommendations of exercise for people with ME/CFS.

Treatment They suggest that if something similar to what happens in diabetes in terms of neuropathy/vascular issues is happening, then the drugs developed for helping the problem in diabetes might help. For example: I'm getting tired, so will have to stop reading. But I'd be interested to...

Re anosmia (loss of the sense of smell) More on the microvascular hypothesis: I thought this was interesting about a link between nerve damage and 'vein wall signalling' in MS. (I'm not sure what vein wall signalling is actually doing though.)

I wondered that @Trish, but we've come across Bruce Patterson before. His solution to Long Covid does not involve apheresis e.g. USA: InCellDx Dr Patterson - New lab service offering cytokine tests to Covid longhaulers

Or, indeed, in anyone else who prefers their medical interventions to have some rational basis.

Discussion of a treatment to filter microclots from the blood (apheresis) has been split off to a new thread: Aphaeresis/ Apheresis (for removal of microclots)

PRS

I've had good feedback about @Michiel Tack's and Evelin's recent article about the PACE trial and more when I've given it to people for this purpose. https://mecfsskeptic.com/a-historic-change-for-the-me-cfs-community/

Thanks for your ongoing efforts @tuha.

From BPS attempts at psychologizing Long Covid @Art Vandelay I agree that quote is a bit worrying, and doesn't really fit well with Avi Nath saying that they found immunological abnormalities in the small sample of ME/CFS patients looked at in the intramural study. Dr Michael Sneller is not...

There appears to be some 'reimbursement for time': The blog that is linked on the information page actually comes across really well. Note that this is BMJ Health and Care Informatics. So, a fairly specific journal.

It's worth getting copies of letters from specialists and GP records. Some practices now have records that can be viewed by patients - which seems to be a very good move towards transparency, and allows for errors to be fixed. It is amazing to me how wrong medical records can be, and so often...

Credit to Sonya and her team, they are working on getting the message out.

A post about a large German epidemiological study has been moved to Long Covid epidemiology (prevalence, incidence, recovery rates)

From the study that @lycaena linked to: A huge study, but with a 3 month minimum, it's a bit early to know about medium term impacts. Hopefully they will follow up.