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 …

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Severe ME Day – 8th August – Tower of London Poppies Trip!!

Hello! Foggy wanted to do something special on Severe M.E day and he chose a day out in London. As London is very hectic and noisy it is 100% somewhere ME sufferers feel the full extent of their illness. One of Foggy’s campaign objectives is to do things that M.E sufferers either find impossible or …

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Ridiculous idea but….let’s put a positive spin on M.E.! (Just for a moment)

Hello! I’m hijacking Foggy’s blog again! Now, I know that it is crazy to say there is anything remotely positive to be said about M.E. BUT, this weekend made me realise that there are some good things to be said for enforced chilling out as much as possible. This is what happened… I went to …

Read moreRidiculous idea but….let’s put a positive spin on M.E.! (Just for a moment)