ATOS Tells CP Woman Her Disability Expected To Improve
September 12, 2013
I’ve been hearing about the case of Amy Jones all week. I thank the Huffington Post for the coverage.
I’m extremely scared by her case, as well as shocked. I have lived with CP myself all my life and, in the words of Jack Carroll, “it’s still here!” and it ain’t going anywhere fast.
I’ve seen people with CP get worse over time. I’ve seen people with CP die as a result of complications.
Anyone can tell that Amy Jones does not have a mild case of CP, just by reading the details of her case. It is just unbelievable that someone who called themself a medical professional thought it would improve after actually seeing her,
And as for the reassessment every six months? Don’t even get me started.
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Same Difference 
the artist taxi driver calls ian duncan smith by mrsuperbafrango and although his language is strong he is spot on
IDS is very lucky to be in politics as where i grew up in London people like IDS were always shunned mainly for their selfish attitude
https://www.youtube.com/watch?feature=player_embedded&v=aF7jNlm-cW8#t=66
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