Jenn - I do not consider spasticity a sensory sx. It can greatly affect walking, sleeping, sitting, ADL's, etc. It might be worth a try to persuade your neuro to let you try IVSM just this one time to see if it helps. It could help calm down a lot of things all at once like the internal stuff, too.

hey Fin,
HUGSSSSSSSSSSSSSSSSS many HUGSSSSSSSSSSSSSSSSSss

you describe how I feel too some days, just sometimes these sxs are too much. I am undx and that part makes it hard too, as I do not call drs much... and just push on and on....

good luck with the neuro office call!! Hoping you have some better sleep nights and better days.. hugssss sorry you are hurting... luv and hugs, sarah

((((((Finlady))))))...There are days I just hate living with this disease. It STINKS!!!!!:mad:

Holly, I'm in enough pain I'm willing to do the IVSM without seeing anyone. I'm usually not that way, LOL! If they suggest it, I'm a going! It's been maddening. :Crazy 2:

Sally, I agree :hug::hug:

Sarah, :hug::hug:

I'll see him tomorrow around 4. They had an unbelievable cancellation and squeezed me in. :eek:

UPDATE:

I believe the phrase that comes to mind is...be careful what you wish for....

Saw the neuro and have some blood tests scheduled for tomorrow. He wants to rule out some nastier things, but he thinks that from the way it's presenting itself the pain might be Fibro. :eek::confused:

He did prescribe baclafon for now in hopes that it will help me with the pain. After the results come back, next plan of attack will come.

:grouphug::grouphug: