Hello from Sudbury Ontario

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Hello from Sudbury Ontario

Postby muss60 » Sun Nov 22, 2009 4:20 pm

My husband was diagnosed with MS last June (2008). Joined this forum to help gain as much information as possible. We saw the CTV special last night. Trying to stay realistic and calm about all this but it's the first real breakthrough and we feel so positive about. We'd give both left and right arms to participate in Dr. Haacke's study in Hamilton. I wish we could get in on it yesterday!
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Postby DM » Sun Nov 22, 2009 7:46 pm

Welcome to another Canadian. I'm in Ottawa. Diagnosed a bit over 2 years, but no symptoms.

Welcome to the site. Haven't seen the show yet but have it on the PVR.

Will get to it this week sometime.
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Postby cheerleader » Sun Nov 22, 2009 8:59 pm

Welcome, muss- I started on here over two years ago when my husband Jeff was diagnosed. We were the Californian family you saw in the CTV doc last night. Couldn't have done it without the wonderful support of this incredible community. Hope you find some anwwers for your husband, and some support for yourself. Hang in there!
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
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Postby RedSonja » Mon Nov 30, 2009 7:35 am

I visited Sudbury a few years ago. Looks like the surface of the moon, only with a million little freshly planted trees. A fantastic trip down the nickel mine. An amazing museum, called Canada North, I think. Brilliant place.

At Christmas we call the cousins and ask how much snow they've got. "Not much, just up to the windowsills." Wow!
Bibo ergo sum
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