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@loulou 

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loulou

canadian MS'ers

Hello to anyone who Lives in Canada, Im going to do a little googling later but It would be nice to hear from the horses mouth How is the MS support in Canada do they have motability do they have DLA or something similar How does the climate affect you How easy is it to live in Canada if you have MS any answers to these questions would be most appreciated or friend request me and we can chat Thanks in advance if anyone can reply x
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@loulou
@loulou
 

hi there Ive noticed a few Canadian Shifters on here lately, Id really like to say hellloooo really appreciate it if you could get in touch loulou xxx

@loulou
@loulou
 

Aaahhhh Calgary the Calgary Stampede!!! Im dying to go! thanks for posting, I was diagnosed just like that after being investigated for what I thought was a trapped nerve in my shoulder it was just "Wham" you have MS after an MRI !!! It must be awful being in limbo for ages I want to know whats going on with my lesions but Neuros dont seem bothered with PP's it seems, Ive had only one MRI years ago and I wan another to see where Im at. Do you suffer with the cold? Id love to chat so friend requested you many thanks Loulou x