I love when I have the energy to do this. The human body is so facsinating and complex. I used to watch this francophone TV show as a kid “Il...
Definitely had these two a lot. I’m sure the attribution error is unfortunately way too common for ME, especially in the UK. On the anchoring...
Is this a possible factor in sound intolerance. I really have no clue what this article is saying but this jumble of words sounds relevant.
To me it would be more about being more considerate of the cost/benefit ratio of anesthesia and surgery, w.r.t. PEM. Taking into account OI and...
These stories are hard to read. Because as someone with severe ME, you know this is the rule, not the exception. How many thousands, tens of...
Abstract: Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a complex multisystemic disease, with post-exertional malaise as the...
Like given how high salaries are in the US, and how high medical costs are too. An upper (“middle”) class getting severe ME from COVID, requiring...
I think this comment by @forestglip is really good:...
Have you elaborated this anywhere? Would love to read more.
They used Fukuda, CCC, and IOM. Severe ME/CFS meant someone met more than one of those criteria. So I’m assuming those who met just one is mostly...
Thank you @Wyva . Very useful article and the translation from Hungarian works flawlessly.
I’m not sure I understand what you mean.
I think the paper might be overstating some findings in general. But this is genuinely interesting. Would like to see it compared to other chronic...
Also does the post deserve it’s own thread. I feel like it’s pretty big news about the Columbia ME/CFS shutting down.
Anyone got a removed paywall link?
I just want to pop-in here and send solidarity to anyone affected by the recent news. It sounds awful. I don’t have the energy to read this...
Looking at central sensitisation literature myself, and it’s quite fascinating how it became such a dominant paradigm for chronic pain conditions....
Possibly, who knows. It’s already quite an assumption to presume T-cells respond the same way to exertion in people sick with ME/CFS and healthy...
She definitely does for long COVID, so ME/CFS wouldn’t surprise me.
Did you ever do this? If so could you send a link? I’m trying to find something comprehensive to send my dad to explain his claim that...
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