I can't read this without a smile on my face and shaking my head in agreement. In this [Read More]
August 8 is Severe M.E. Awareness Day. A day to give a voice to the millions of people [Read More]
May is ME Awareness Month and once again I am participating in the virtual campaigns online to help [Read More]
Have you ever experienced that moment of intense pain in your eyes and head when you've opened the [Read More]
I came across this fantastic list of guidelines for how to live successfully with Myalgic Encephalomyelitis and just [Read More]
Who am I? When living with severe chronic illness it can be easy to feel like you've lost [Read More]
What Is M.E? How To Get By Advocacy Tools M.E. Directory We in the ME community are so [Read More]
When I was first diagnosed with Chronic Fatigue Syndrome, I felt lost. It's a condition I had never [Read More]
When I first got ME/CFS, I was so utterly exhausted, I slept many hours a day and I [Read More]
It might surprise you how often people with chronic illness are asked what they do with all the [Read More]
Every Wednesday the ME community comes together on Twitter to raise awareness of this debilitating chronic illness. We [Read More]