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

On caffeine, masochism and deer

On caffeine, masochism and deer

I've been posting blogs on Tuesdays and Fridays for at least the last couple of months and it seems weird to let a Tuesday or a Friday go by without posting something. This isn't a big newsy post or a useful post. It's barely even a Camp NaNoWriMo update. I've gotten so out of the … Continue reading On caffeine, masochism and deer

Acceptance and self-care during the tough times. Click to read some ways I look after myself, living with a chronic illness. #selfcare #chronicillness

Acceptance and self-care during the tough times

It's been ages since I posted a personal update here, so I figured it was time. The last little while hasn't been great in some ways. My health has been not so good, even by my standards of ongoing not so good health, but it took a serious dive about a week ago. The background … Continue reading Acceptance and self-care during the tough times

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