Frequently Asked Questions About Myalgic Encephalomyelitis
As this community grows I get more and more questions about certain words or acronyms I use in my writing and graphics, so I thought I would create ... Continue
You Might Be An M.E. Sufferer If… (Part 1) Guest Post By David A Graham
I can't read this without a smile on my face and shaking my head in agreement. In this three-part series our guest author, David Graham, shares his humorous ... Continue
A Poem About Life With Severe Myalgic Encephalomyelitis
August 8 is Severe M.E. Awareness Day. A day to give a voice to the millions of people around the world who are living in isolation and torment ... Continue
My Chronic Illness Story: How I Became Housebound With Severe M.E.
May is ME Awareness Month and once again I am participating in the virtual campaigns online to help raise awareness of this life-destroying illness called Myalgic Encephalomyelitis. Today ... Continue
Get Your Own Personalised Millions Missing Poster For ME Awareness Month
May is #MEAwarenessMonth and I thought, since many of us cannot go to the live #MillionsMissing events in person, I'd like to help my fellow people with ME ... Continue
Photophobia: 6 Ways To Cope With Light Sensitivity
Have you ever experienced that moment of intense pain in your eyes and head when you've opened the curtains on a bright and sunny day? Anybody who has ... Continue
Where To Find ME Awareness Pictures
Have you been searching for graphics to easily share with friends and family what Myalgic Encephalomyelitis is really like? Would you like to share relevant and informative infographics ... Continue
How To Have ME Successfully
I came across this fantastic list of guidelines for how to live successfully with Myalgic Encephalomyelitis and just had to share it. It's so refreshing to read a ... Continue
Living With Severe ME/CFS, Who Am I Now?
Who am I? When living with severe chronic illness it can be easy to feel like you've lost your identity. When experiencing a loss of identity, you start ... Continue
Advocacy And Fundraising Ideas And Resources
What Is M.E? How To Get By Advocacy Tools M.E. Directory We in the ME community are so grateful that you are interested in supporting our cause. Thank ... Continue
A Community for ME/CFS Bloggers and Patients
When I was first diagnosed with Chronic Fatigue Syndrome, I felt lost. It's a condition I had never heard of before and my doctor didn't seem to know ... Continue
How I overcome insomnia
When I first got ME/CFS, I was so utterly exhausted, I slept many hours a day and I slept at night too. Later I was introduced to one ... Continue
Imagine… A Day in The Life of ME
It might surprise you how often people with chronic illness are asked what they do with all the free time they have at home. I think many healthy ... Continue
ME/CFS Awareness Pictures To Share, Part 5
Every Wednesday the ME community comes together on Twitter to raise awareness of this debilitating chronic illness. We share recent media coverage, research news, our personal experiences and ... Continue
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