Seeing My MP

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Seeing My MP

Postby jacf47 » Tue Mar 20, 2012 9:07 pm

Hi All
I am going to try and raise awareness to people who suffer from Fibromyalgia by seeing my MP do you have any useful information I can tell him as well as my treatment by DWP in the last 9mths
look forward to seeing you comments
Thank you
Jacquie :-D
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Re: Seeing My MP

Postby denys » Tue Mar 20, 2012 10:17 pm

:goodluck1: take a copy of one for the non-believers and the spoon theory plus stuff off the NHS website might give them an insight as to how things affect an FM sufferer

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