Hi. I am a Canadian. Healthcare is managed provincially so there are probably different answers for different provinces, but I was wondering how any other Canadians were finding the healthcare system with their MS?
My sister has been DX'd for 15 years. She spent the first 10 in Alberta and the last 5 in Manitoba. The way she has been treated has left her totally paranoid... as she tells it. Maybe the paranoia is part of her MS because she does have multiple lesions on her brain and has a lot of cognitive dysfunction.
Being in Limbo myself right now, I am wondering if I should take her paranoid (do not trust any doctors!) attitude to heart or if real help is available.
My sister has been DX'd for 15 years. She spent the first 10 in Alberta and the last 5 in Manitoba. The way she has been treated has left her totally paranoid... as she tells it. Maybe the paranoia is part of her MS because she does have multiple lesions on her brain and has a lot of cognitive dysfunction.
Being in Limbo myself right now, I am wondering if I should take her paranoid (do not trust any doctors!) attitude to heart or if real help is available.
Comment