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#1 | |||
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Junior Member
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Jensequitur there, Jensequitur everywhere!
Just poking my head in to say howdy and how-ya-doin... I see some familiar faces! Good to see you again. Diagnosed in March 2007 with relapsing-remitting, but like many, I've probably had it for years. Currently on Copaxone and hating it, but it's better than the alternative! And I'm in remission... ah, remission! I'm going to enjoy it. And do as much stuff to the house as I can, because who knows how long this will last. |
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"Thanks for this!" says: | Curious (01-23-2008) |
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#2 | |||
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Senior Member
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I have RRMS and am 39 years olds. I was dx'd 14 years ago (after 6 years of flares) but looking back I know that I have had MS since my teens. I was taken out of work over 6 years ago. I spend my time taking care of my beautiful daughter and husband, reading books and getting together with friends.
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"Thanks for this!" says: | Curious (01-23-2008) |
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#3 | |||
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Member
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Well,I was diagnosed probable RRMS on Sept 21,2007,I will never forget that day that's for sure. I'm probable because in Nov of 2006 I was Dx'ed with Optic Neurtis(had no insurance at the time thank goodness I do now) and I've only had one flare-up(ON) and you need 2 for a definate dx's of MS,yet I have enough lesions in my brain for a clinical dx's and have 2 lesions in my cervical spine. I started taking Copaxone on Oct 16th last year so far so good.
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Diagnosed Probable MS 9/21/07 . Started Copaxone 10/16/07 3-6-9 the goose drank wine the monkey chewed tobacoo on the street car line the line broke the monkey got choked and they all went to heaven in a little row boat... . |
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"Thanks for this!" says: | Curious (01-23-2008) |
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#4 | |||
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In Remembrance
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I'm having a hard time keeping up, but just wanted to welcome all of you to the Neurotalk MS Forum.
WELCOME ALL.. ![]()
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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