For those living in Wales there is a Vasculitis Support meeting on the 21st January. Emma Hughes from Genetic Alliance Rare Disease UK will also be at this meeting and will hopefully be able to update members of the Rare Disease Strategy and the WHA and also where to go for help and advice if you are having problems accessing treatments or medication. Please follow this link for more details. vasculitis.org.uk/events/so...
Wales Vasculitis Support Meeting January 21s... - Vasculitis UK
Wales Vasculitis Support Meeting January 21st 2017
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Suzym2u
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Thanks Susan, I always forget to share the events here 
I've created it as an event on Facebook too, if that's easier for people to share:
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