ME and the truth: The reality of Myalgic Encephalomyelitis. #chronicillness #spoonies #myalgicencephalomyelitis

ME and the truth: The reality of Myalgic Encephalomyelitis

In July 2017, I wrote a post entitled ME and me: Living with Myalgic Encephalomyelitis, in which I talked about my experience of life with an often misunderstood and misrepresented chronic medical condition. Since then, I've had so much wonderful feedback resulting from that post, and one random person telling me that I can be … Continue reading ME and the truth: The reality of Myalgic Encephalomyelitis

ME and me: A tale of life with Myalgic Encephalomyelitis

ME and me: Living with Myalgic Encephalomyelitis

EDIT 14TH MAY 2018: I've written a more detailed post about the symptoms of ME, which is less about my personal experience and more about explaining the condition in more medical terms. You can read it at ME and the truth: The reality of Myalgic Encephalomyelitis. Sometimes I mention here about being sick, being disabled, … Continue reading ME and me: Living with Myalgic Encephalomyelitis