So, some people might think it’s weird for me to post about this on a blog that anyone can read but meh, to me it’s not something I feel I need to keep a secret and it could probably be helpful for me to talk about as I’m sure there are some amongst you lucky offer holders who do or will experience similar circumstances. So this blog is about my year leading up to my CFS/ME diagnosis.
What is CFS/ME I hear you ask? CFS/ME stands for Chronic Fatigue Syndrome/Myalgic Encephalomyelitis. They are two names for the same condition and it’s up to the sufferer which one they use… I personally prefer to say that I have CFS as it’s less confusing and it makes it easier for other people to understand.
