The Caged Bird’s response to The Lancet 14.01.15

The “Caged Bird’s” Response to M.E. Disinformation Campaign by UK Psychiatrists”


The following is shared with permission from a friend who doesn’t wish to be named….but let’s call her ‘The Caged Bird’

If you want to snuggle down with a cuppa and read her words of wisdom I’d be ever so grateful and please share across social media too the greater awareness we create the sooner we can stop having to fight this battle we have…thank you.x

“Hello, folks. WELL … after a somewhat trying day, one awoke to yet another useless, ignorant, arrogant and dangerous article on how ‘exercise is good for ‘CFS/ME” and how we with ‘CFS’ fear it making us worse so we are essentially to blame (as well as it being ‘all in our minds’, for the most part – which of course is why we are banned from donating blood and organ; in case we pass our ‘madness’ on … You’re laughing at the stupidity there…

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About The Other Side Of The Stretcher

Nurse turned patient, but not by choice. I was became a Registered Nurse in 1985 when I was 21 years old. That career was cut short the end of 1994 when I was unable to work anymore because of the illness M.E. or Myalgic Encephalomyelitis. I have 3 adult children including twins, A daughter and 2 sons. View all posts by The Other Side Of The Stretcher

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