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#1 | ||
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Senior Member
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I am in awe over the dedication of the wonderful MS specialists that spend their careers working on this miserable, thankless disease.
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He is your friend, your partner, your defender, your dog. You are his life, his love, his leader. He will be yours, faithful and true to the last beat of his heart. You owe it to him to be worthy of such devotion. Anonymous |
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#2 | |||
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In Remembrance
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I use to hate it when I'd get an upbeat report from my Neuro.
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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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#3 | |||
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Senior Member
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I had a similar experience recently. I knew I wasn't doing well in recent months, and still the MRI at the end of December showed an improvement (fewer lesions than in 2001). Whoopee! Celebrate! I get to stay on Copaxone because it's "obviously working" as the neuro stated.
I had a really interesting fall a few weeks ago (no broken bones--celebrate!) with my glasses bent all out of shape, a cut, a black eye, and several large bruises. That's just an example of why I know that an MRI doesn't have much of a relationship to a person's symptoms--and the experts admit that.
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Repeal the law of gravity! MS diagnosed 1980. Type 2 diabetes, osteoarthritis, osteopenia. Avonex 2002-2005. Copaxone 6/4/07-5/15/10. Currently: Glatopa (generic Copaxone), 40mg 3 times/week, 12/16/20 - 3/16/24 |
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