Ten Ways To Prove That Exercising Will Not Cure ME/CFS https://www.healthrising.org/blog/2...exercising-not-cure-chronic-fatigue-syndrome/ by Cort Johnson Your family, friends and even your doctor may, probably will at some point, prod you to get moving. They think that if you can just get on your feet again and start exercising, you’ll be so much better. It’s irritating to hear and just reinforces how isolated you are and how little they understand what you are going through. You have to cut them some slack, though. You may, after all, look like you’re the picture of health. Plus we all intuitively sense that exercise, in general, is good for us and bedrest can make things worse. From the outside exercise might look like just the ticket. They are only trying to help. Well, exercise is a ticket – but usually not to better health. While people with ME/CFS – like anybody with a chronic illness – should make every attempt to maintain their fitness, vigorous or even light exercise almost always has negative effects. But how to convince your family, friends and even your doctor of that? It may take some hard evidence. Below are some suggestions that may help some well-meaning friends, family members and even doctors understand about exercise in chronic fatigue syndrome (ME/CFS)...
Hmm. It's OK. It's really just a list of the evidence that exercise in ME is harmful, GET doesn't work, and some suggestions about pacing and other approaches to 'exercise' in ME. I will not be recommending this article to anyone as it seems to me to be just a cobbled together article wrapped around repeated ads asking for money for the author.