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08-06-2007, 10:35 PM
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#121 | |||
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Junior Member
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Greetings!
 Just joined this forum, and am happy to report that though I was diagnosed with R/R MS in 1993,I've been very lucky and haven't had too a bad time of it. Ten years after my diagnosis,when I had some fleeting visual disturbances , my neuro had me get my first MRI since then. He said that the progression was slight enough that it looked almost like a new case, and recommended therapy to try to keep it that way. I've been on Copaxone for 4 years,and my only real side effect has been those dam lipo atrophy site dents(arms, thighs).I know I probably should not do this, but I only shoot my butt now-- WTH, it looks like chewed bubblegum anyway  (I'm 51) As for the disease and symptoms,(though I HATE the heat and do tire occasionally)nothing really major since '93, and thus far, the Copaxone seems to be effective. Cheers! 
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08-07-2007, 11:25 AM
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#123 | |||
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In Remembrance
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Hi Bee, Welcome to your home away from home.
I'm glad to hear that you are stable early in the game. I hope Copaxone keeps doing it's thing for you. Jump right in and enjoy your stay. 
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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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08-07-2007, 01:39 PM
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#124 | |||
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Wise Elder
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Hi, Bee! I'm glad you migrated over to the fun people! We are the coolest group on the boards! Don't believe me? Wait till the others read this.
  
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—Cindy For every day I choose to play, I set aside a day to pay. —AMN "Sometimes plastic wrap just won't cling, no matter how much money you put in the meter." —From the Book of True Wizdom |
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08-07-2007, 02:31 PM
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#125 | |||
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Senior Member
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Quote:
 Hi Bee!  AMN is NOT prone to overstate facts, so , if she says we are fun  and  cool these are the most understated facts you'll hear from this group!   Welcome to the group!  Glad you are here.
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-- Beth RRMS -dx 1997 Never doubt that a small group of thoughtfully committed citizens can change the world; indeed, it's the only thing that ever has. - Margaret Mead Breathe In HOPE, Breathe Out DETERMINATION |
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08-08-2007, 04:21 PM
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#127 | |||
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Senior Member
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Hi Bee and welcome to the group! I'm glad to hear your MS hasn't progressed very much and the copaxone seems to be working. I was diagnosed in 1990 and am using a wheelchair.
 See you around!!
__________________
_____________________________________________ .....Judy SPMS -- FIBROMYALGIA -- Ouch! and Ouch! . |
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08-14-2007, 08:00 PM
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#128 | ||
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New Member
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Newbie here.
Dx'd with RRMS this year after years of thinking my symptoms were all in my head.... (no pun intended). Anyway, just wanted to say hi to everyone and introduce myself. KathyM told me about this place months ago, sorry it took me so long to get here. |
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08-14-2007, 09:31 PM
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#129 | |||
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In Remembrance
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Hi Chelle, Welcome to NeuroTalk and nice to meet you. Do I know you from someplace else? I don't recognize your name.
So sorry for the DX, but guess it's a relief just to know. Are you on any of the MS Meds yet? Just join in anywhere and have a good time.
__________________
~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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08-14-2007, 09:47 PM
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#130 | |||
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Magnate
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Quote:
Glad you finally made it here!
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| Closed Thread |
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Thanks for the Welcome!
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