Article: Verywell: Exercise for Fibromyalgia and Chronic Fatigue Syndrome

I'd say about twenty years before it is significant.
Definitely quicker than this for severe bed-bound patients but that's about 10% or so. I've never been bedbound, thankfully. Plenty of otherwise healthy people are actually less active than I am even at my sickest. Some people really hate moving around and yet they are merely highly sedentary, deconditioning simply doesn't work like that.

But then again we are dealing with people who keep mocking us for "staying in bed and pouting" while also being "relatively active" during PACE trial and as such not needing actimeter testing since we clearly are sedentary, not pathologically deconditioned. Wearing an actimeter is obviously too much of a burden but clearly it can't be actual patients doing all those FOI requests and writing to medical journals since we are so sick.

Tails they win, heads we lose. What a nightmare.
 
It also mentions endorphins as making you feel better, yet my experience of exercise is that I no longer produce endorphins when I'm ill. It was the first sign that led me to ME as a diagnosis. Has anyone else noticed that?

Yes, but this was only during the viral onset. Years later after a diagnosis of ME (when I was improving) the endorphins came back and I felt like a million bucks after a 30 minute jog, until the next day of course when PEM set in.
 
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