May 12th, 2017
Today is International CFS/ME Awareness Day, and as someone who has been living with the condition for a long long time, I figured it is time I spoke about it on here.
For the most part in this post I’m going to talk about my own experiences with the condition. If you’re not up for a long read, feel free to skip reading this. If you think you’ll find this post helpful, grab a brew, because you’re about to hear my life story.
August 3rd, 2016