Ok, so my left side is primarily affected by my MS.

Always has been, thought it always would be.

This weekend my right hand has been acting stupid.

Specifically my right index and middle finger. They are spazzing out and acting like it is rebelling against my body.

Don't like this.

School starts in two days and I need it to type...

GRRRRRRRRRRRRR.

Sorry Earl....I hope it's just a temp thingy and not the start of a flare.

I get temp things on the right side now and again, and they go away after a short bit. My sx are primarly left sided as well. those are the ones that stick around.

Ugh. It's a party and every nerve is invited. Hate it!

If it keeps up, are you going to call your doc?

Sometimes I feel like I'm on my last nerve.

Everything gets on my nerves.

Just when things start to get better, something comes along and snaps my nerves.

Right now it's my right side that's being mostly affected, with a little bit of left sided crap going on (mostly the left hand). Hey, together we could make one (mostly) working person!

I hate it when the MS screws around with my hands. I'm a crocheter and a knitter. Doing my yarn hobbies is what keeps me sane and keeps me from stabbing annoying people in the eyes with a crochet hook. (everything is getting on my nerves, and I'm so close to poking someone's eye out with a crochet hook or use my metal knitting needles to make a voodoo doll out of the next person who annoys me)

Dont you hate it when the MS screws around with your ability to work or do your hobbies?

I hear ya,Earl. I've only mostly had left sided symptoms too. The past week or so I've noticed some slight numbness in my last two fingers on my right hand. I've never had any numbness before in my fingers or arms. Some weakness overall, but never numbness in my fingers. A lady that lives on my street said to me the other day that one day they ( I say they because I wasn't born til 1970) woke up one day to a cure to Polio. Why, oh why, can't we wake up to a cure for MS one day soon?!? Like yesterday would be great. I'm not a hateful person, but MS I hate with every ounce of my being!

This is so well said but there is alot of money involved 30,ooo dollars per person us funds not counting all the canes ,walkers,wheelchairs and all the other high priced accessories.Is it any wonder that a simple study for ccsvi is being pushed to the side.Take a look at the Neurologist office pens,pencils and posters can you imagine all the perks you dont see.Sorry for all the new symptoms Earl and all reading this. We Will Never Rest till this monster is finally slain....because M.S. never rests ever....

I have to agree with you,Jeep. I know everything boils down to money. That said, I won't stop asking questions nor give up hope. I'm very stubborn which at times has come in handy and other times, not so much.