For anyone who has been diagnosed with post-viral fatigue syndrome (PVFS), chronic fatigue syndrome (CFS), or myalgic encephalomyelitis (ME), and refuses to accept the diagnosis, this post is for you.
I first discovered that something wasn’t right with my body in April 2010 when I fell very ill with a virus. My entire body ached for two weeks – my muscles, my bones, everything from the top of my head to the tips of my toes. I couldn’t stand to be touched. It was like the all-over ache people get with the flu, but a hundred times worse. The only fever was on the first day and I didn’t have any other symptoms, except for extreme fatigue.
