wink     ;)

chronicallyscrewed:

A lot of people don’t understand how I can be so dismissive about information regarding CFS/ME. When they try to shove the newest ‘cure’ or newest ‘possible cause’ under my nose, I shrug it off. I am told that I am being negative, or that I want to stay in the dark. But really? I’m just trying to help myself out…

This too.