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49 minutes ago
Invisible: A New Look at M.E. by Anne Nicholls

"Dear Everyone, my exhibition of art, poetry and facts is called Invisible: A New Look at M.E.

"It's at the Artrix, Bromsgrove, B60 1GN, from the 4th April to the 20th May.

"I hope people will ... See more

A picture's worth a thousand words, they say. But how to show the invisible? How to explain our experience when so many people discount Chronic Fatigue Syndrome as a psychological problem, if not ... See more

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1 hour ago
Majority of disability benefit claimants left with not enough to live on, campaigners warn

“This is a damning indictment of the Government's treatment of sick and disabled people,” said Debbie Abrahams, the shadow work and pensions secretary.

“It is shocking that people on ESA are ... See more

Some 60 percent of people claiming the main long-term sickness benefit believe the amount of money they get is not enough to live on, according to a major new survey. Labour called the findings from ... See more

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1 hour ago
Plymouth girl wants everyone to watch this film about her illness

10 year-old Shannon Tiday, "Is it ok if I ask you big favour?

"There's this new film Unrest. It's very important and shows this lady is very brave with ME. It shows that ME's not in your head. It ... See more

Shannon Tiday has been dealing with ME since she was just a toddler

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19 hours ago

I'm not sure if this is the right place, but a while ago there was a quote circulating the facebooks of many ME-folks, which said something along the lines of "there is nothing you love that this ... See more

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