Member Stories

This is the name I use to “explain” the many diverse symptoms of the disabling and debilitating illness M.E./C.F.S. to people who stare at me blankly looking for a “sign” somewhere on my person that indicates to them I really am ill, and to try to give this complex and very misunderstood disorder, the recognition ...

Hi everybody, I'm Sunsetleigh. I am a ME sufferer and also have Fibromyalgia as well as a lot of branched off things. I have been ill since I was about 10, and was constantly told by doctors that ...

I have been sat here staring at a blank computer screen for what seems like forever. How do I begin to express in words just how this devastating illness has altered my life story?

I was an academic type, quick thinking, forever active, independent and in control. I had spent ...

Hello my name is Tigger and here you can read about how I think I got M.E/CFS. During my childhood I was never a well person any cold or virus or infection that went round ...

I have had this dreadful syndrome since 2003. It started with tonsilitis and I was ill for 4 weeks. My first day back at work and I collapsed on ...