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RRMS to SPMS how did you get there?

 
 
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Old 04-03-2010, 12:23 PM #26
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Kitty Kitty is offline
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Kitty Kitty is offline
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Join Date: Jan 2008
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Quote:
Originally Posted by Dejibo View Post
I have been dx in 2006, but can trace back my first huge flair to 2001. that makes 9 years for me.
My first BIG flare was in 2003. Both of my legs were numb and I assumed I had a pinched nerve. No other sx....jut the numbness. So I guess I've actively had MS for about 7 years.

It was two years after that first big flare that I had my second (even bigger) flare. Double vision, numbness, balance, etc.

I tend to think I'm probably SPMS, too. But, my neuro hasn't changed my dx status.

Right now it seems that the visual sx are what I predominately have. If I had to choose, I would have something be numb (besides my right hand/arm. It already is.). Visual sx are awful.....they affect every aspect of your life. Not saying the numbness is any fun.....but at least I can see where I'm going.
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"Thanks for this!" says:
barb02 (04-03-2010), Dejibo (04-03-2010), SallyC (04-03-2010)
 

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