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.
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goodness THIS. People think...new research. The thing is I don’t understand
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