Wednesday, February 10, 2010

Best source for ME/CFS News, Forums and Chat

I'm super sick. There's so much I'd like to share but I can't sit up at the keyboard for long enough. For now, I want to send everyone to for excellent and swift coverage of medical, political and social developments regarding ME/CFS. This is the best place I've found yet for information and discussion and yes, thank you Phoenix Rising, for the hope to keep going.

EDIT: I've been less able to frequent forums since I first posted this, partly because of cognitive challenges, but I'm realising that the brain fog is exacerbated by the in-fighting that sometimes happens between patients and patient groups. If you do chat on forums, be cautious and be kind.