What 'neuroscience' is this then? If this 'faulty alarm signal' / 'fight or flight' loop is your preferred hypothesis, that's fine. But what neuroscience backs up this explanation? And why wasn't this claim challenged?
Ok. I shouldn't have posted last night without explaining why the paper struck me as potentially problematic. It was getting late and I needed to come off the laptop.
I have many questions and would not claim that this paper was potentially not authentic without first doing a bit of digging...
https://meassociation.org.uk/2026/05/new-provider-announced-for-kent-and-medway-me-cfs-and-long-covid-service/
MEA reporting that Cora Health, a private equity-backed company that has a number of NHS contracts, has won this award.
https://www.nhsforsale.info/private-providers/cora-health/
(opens in new tab)
Interleukin 6 as a Treatment Target for Depression
Visual Abstract.
Importance Interleukin 6 (IL-6), a keystone inflammatory cytokine, is a credible mechanistic candidate for causing depression. However, randomized clinical trials testing its treatment potential remain...
I have researched vision issues a lot because they are some of my most disabling symptoms, although this is largely due to my having visual snow syndrome on top of ME.
The optic nerve is just one part of the visual pathway — the other parts are the eyes (the retina, in particular), and...
I'm also a male with PoTS but it's just a well known fact that this is a highly female predominant condition. The figures cited are usually somewhere in the region of 75–85% female predominance, although some studies are higher than that (like this one).
Just a minor correction for Bogus Bruce P:
https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2026.1832958/full
"In the published article, there was an error. In section Materials and Methods, Patients, it was indicated that a total of 144 individuals were enrolled in the...
I noticed the insane amount of references. Douglas and co seem to publish a lot (in any old journal), and I'm not convinced it's of the highest quality.
Yes, I think parts of Unrest are certainly dramatized. In fact Jen Brea in my opinion does not look like a typical ME/CFS patient. The fits and collapses are not representative of my experience. I suppose we only saw the 'highlights' (or 'lowlights' perhaps). Most of us are much more boring than...
I feel like this could work / be helpful, but only if the HCPs were in that role-play scenario for a whole day or even several days — not just a few minutes like if you wanted to simulate blindness.
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