During my first flare this is how I described my leg to feel. I am used to it now.
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Sasha - dx January 2011; tysarbi, zanaflex, gabapentin, and baclofen
~Life is not about waiting for the storm to pass, it is about learning to dance in the rain.~ -
Huh?
When everyone speaks of this being 'spasticity' it kind of throws me. I had a different idea of what spasticity would be.
I feel my legs are weak mostly and I feel kind of like a wooden soldier. No grace to my walk, no balance. I also feel like someone is standing on my shoulders weighing me down.
Does this make any sense?
I honestly didn't feel this way prior to starting Copaxone 8 mos ago. I've never felt as bad with my MS prior to that.
The other med that seems to give me fits is Nuvigil. Anyone have problems with that? I get jittery *on 150mg* and agitated.
DianeYou cannot dream yourself into a character; you must hammer and forge yourself one.
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