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04-05-2010, 05:31 PM | #1 | |||
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Elder
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Hi all,
Saw the neuro this afternoon. After discussing sxs returning after IVSM, and my balance getting even worse, we discussed what to do. He feels that the MS is "changing". Suggested a clinical trial, so I begin after the Copaxone is cleared from my body, around June. He loved my Hawaii tan, by the way...
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04-05-2010, 05:34 PM | #2 | |||
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Grand Magnate
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Do you know what trial he is suggesting?
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"Thanks for this!" says: |
04-05-2010, 05:48 PM | #3 | |||
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Magnate
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Holy crow my neuro says the same thing today. 3 more months of TY then I am off to UVA for trials because she has run out of options.
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04-05-2010, 07:12 PM | #4 | |||
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In Remembrance
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Good luck Debbie, keep us updated...oh and I hate your tan..
Good luck to you too, Leggz.
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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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04-05-2010, 08:17 PM | #5 | |||
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Magnate
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Hey Deb, wanna see if we can do them together? LOL that would be fun, we could be lab rat buddies!
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04-05-2010, 08:25 PM | #6 | |||
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Elder
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It's with Ely Lilly...a subcutaneous injection. Yeah, let's hold hands and be lab rats together!! Or guinea pigs, as I like to think of myself!
Neuro's nurse told us that 6 out of 7 patients receive the med, as opposed to a placebo. And any time that my doc feels it's not helping, he'll yank me from the study.
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