Hi Benny-- simultaneous symptoms on both hands are definitely possible, especially when considering lesions of the spinal cord.
So sorry you're going through this-- whatever it ends up being seems to be setting in fast and furious-- but I'm glad you're in the hospital and they're doing everything they can.
I am 31 with two little people myself, and I know how scary this all is, especially in that context.
Hang in there,
Sadie
thank yall so much.. It defintely hasn't been a fun situation! I had the visual evoked potential testing today.. havent' gotten the results - should in the morning - did yall have those ?
Do yalls muscles ever feel like they are vibrating? My lips, face shoulders, foot feels like it's vibrating at times... and one more question - my hand weakness- hit both hands at the same time - same week, is that normal in MS? my right leg started one week and then both hands.. speech also affected with all of this.. thanks for yallls time!
I have a friend that had meningitis, and he ended up with a little brain damage. I think the inflammation was causing pressure on the brain.
Hi, I am sorry you are going through this. I don't know jet if I have MS, but I have these symptoms, tingling all over, started in one toe June 2010 then got more widespred, soon both feet, then hands in March 2011 and left side of face in April.
Along with getting the tingling I got also nervepain in all these places at the same time. Since this summer, I've been getting muscle twitching all over and musclecramps (painful) first in legs now also in arms. I also get many other things that just stay for a week, month or so. But most of them mild.
It seems like the tingling has gone all over sooner for you, but maby we are deeling with simular "behavior" of the MS or what ever it is. Good luck in this all and please let us know how this turnes out. Sorry for my bad English.
My best,
Dagun
It sounds possible, but unfortunately it can take a while for all the pieces to fit together. It sounds like a scary situation though. Hang in there.
Tammy
I meant to add- both MRI's were done on the not t3 (or whatever that newer technology is) due to my spinal fusion from sciolosis as a kid- so both same technology.. thanks again in advance for any insight!