I think definitely, ess - I always have spasticity in the limb that has the injury.
I don't see how MSers can avoid spasticity, given all these causes!
Not counting exacerbations or progression of the disease, I have SSRIs, fracture, bladder distension, excessive fatigue, and extreme trouble with heat.
I have been wondering if spasticity is going on in my right ankle, the one I fractured badly last fall. Or actually, not the ankle, which moves pretty normally, but the leg right above it, for maybe 6 inches. It feels very stiff, but when I palpate it, the muscles move well.
Am I totally barking up the wrong tree here? Someone knowledgeable, please clue me in.
Thanks,
ess
Before my MS diagnosis, the pain from spasticity was what my rheumatologists thought was arthritis or fibromyalgia. I always hurt worse when too hot or too cold, stressed out, fatigued, but never had joint swelling or the trigger points. I don't know why no one ever directed me to a neurologist back then . . .
Not bitter, but just saying . . .
thanks for riposting this I can't get it to work here at home. probably because its my work computer. for some strange reason it's looking for the network when i open this. I'll try at work tomorrow.
Great information there. I bookmarked that baby.
I had a few things going on ie:constipation, urinary retention, questionable renal stone (doubt it though -- CT Scan would have picked up on that one unless I already passed it). My truncal myoclonus is at its worse today than any other time I've had it. I think with that too, the involuntary jerking can add to the back pain.