I don't know how many of you still get excited when you see articles about CFS/ME. In fact, if you're anything like me, your heart probably sinks a little. After all, it's usually just more confirmation that we're either all mad, or some of us are mad, or none of us are mad but they're not sure how.
I did think this story was interesting though: http://www.bbc.co.uk/news/health-15401746
Mostly, for the very sensible comments of the researchers involved (basically; yeah, it worked. Now let's see if it really works).
Any opinions my fellow sufferers? Or those of you who don't suffer from this?