this spinal one has been coming on for some time now, about a yr or more, and the numbness in my right foot and hand have been coming well in the hand coming and going the foot been constant the numbness I have noticed off and on for about 7 maybe 8 months on right side and have made mention in some post at the other site.

I have had 4 taps and 5 mris all pos for ms 3 by this doc 1 each by 2 second docs yes i got a few opinions on this every time its pos, the feeling i got from the neuro was his worries about if the C was doing its job I only have two years of mris to work with and have been on c almost that time so he said as far as how fast it is progressing he isnt sure

because of the amount of flair ups, and attacks i have had in the past 9 yrs and now he is trying to judge how much more would there of been with out the C and thinks that maybe not much diff my worry is i felt comfortable with C i didnt like the sounds of those others and am not sure what direction to start looking at , sorry i dont have the tech terms for everything

I will say b4 using C he did try to sway me and i dont recall what it was once a week injection I think it was B he felt this was better for my MS bestron or bextron i think i have to look it up again anyway it do seem like i am good for 2- 3 attacks a yr thats how its been for a long time now, so even I have question C and did so months ago because I am still having them at same pace,

so even now i am more confused then i was ten minutes ago when i started typing lol great, some one i know has a sister with MS and she swears by the A one I do believe a med change is in the making here. even he has been looking for some type of improvement on my left side and their isnt any . I wish i knew what to think oh goodie look at the time think I will take steroids now get a jump on the day and maybe by this time tonight i can sleep

cherie I read that page thank you

{{{{{annie}}}}} thanks for the hugs another day for the drawing annie?

AV thank you too

sometimes i just cant get over how nice this site can really be becaue of the folks that are involved, oh how i wish i could go back in time with my sons seizures and find this site i foundchat rooms back then but nothing like this site