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a new way to describe what MS is to me

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Old 01-17-2009, 11:15 PM #1
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kind of weird in a way, its true aint much you can do about it anyway(meaning controlling if we get it or not) call it epilepsy call it RSD call it parkinsons or MS, it something we all have and ...

lala lalalalala live for today....dont worry about tomorrow hey hey ey...

thats what we have to do, it not always easy, thats for sure. I have a long way to go on mastering this at times
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Old 01-18-2009, 01:23 AM #2
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Thanks for your perspective, Sassy.

I often say,
Quote:
MS is just 'stuff'. Everybody has their 'stuff' to deal with. MS is my 'stuff'.
~ Faith
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Symptoms since 01/2002; Dx with MS: 10/2003; Back in limbo, then re-dx w/ MS: 07/2008
Betaseron 11/2003-08/2008; Copaxone 09/2008-present
Began receiving SSDI 11/2008
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Old 01-18-2009, 06:18 AM #3
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Good way to look at it sassy....hugssss
I tend to focus on what I can do, I keep trucking along doing too much at times...(cant stop working although body would love it) and deal with what I got.... whatever mine is hheehee undx crapola!!

hugsss,sarah
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