My only fear was that they would still not see that ME/CFS is just as bad as what they are going through now. I was hoping they would be able to recognize that all these approaches did not work for us either but some of the comments in this article make me think we will be left behind again. She's already set her condition apart from ours.
"Graded exercise, an approach that has been used to manage patients with other post-viral fatigue, wasn’t working;" (It doesn't work for us either.)
"But one thing has been evident for some time: this is not a straightforward post-viral syndrome, and requires a different approach." (ME/CFS has never been straightforward--in no way, shape or form but it sounds like in her mind it has.)
So sad.