‘You haven’t got a ‘never been seen’ illness….’

Sally post again…sorry Foggy! Back in 2007 when I first started with M.E. symptoms and had almost weekly hospital visits trying to establish what was wrong; I, obviously, turned to friends for support. In the most part, I received fantastic support and I will be eternally grateful for the phone calls, girly chats, visits I …

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Lisa’s story

Hello, It is incredibly difficult to describe how debilitating and life changing M.E. is to a non-sufferer. Foggy thinks that having a range of sufferers ‘guest blog’ with individual stories will show the wide range of symptoms and levels of suffering. This particular blog is written by Lisa who has severe Myalgic Encephalomyelitis (M.E). Here …

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Foggy’s blog – from a different perspective – ‘Fighters’

Hello! Foggy has asked a handful of M.E. sufferers to write a blog post so that readers can see/understand how varied and wide ranging M.E. can be. He has chosen someone from each of these areas: Young, severe and ‘recovered’ to tell their story. This blog post is written by an 18 year old young …

Read moreFoggy’s blog – from a different perspective – ‘Fighters’