This Is MS Multiple Sclerosis Knowledge & Support Community

I have just saw the boys and Carrie and one lesion right now is no big deal.

In other cases they have seen the body pop off a couple of lesions, then it stops and seems to go dormant. They never have them again.

I am not showing anything but a bit more spasticity. My strength and dexterity was better but they all agree'd I was not ready for sedimentary work.

So my best ever on drugs was LDN, and Copaxone. In 2 years I didn't have an active lesion when I used them together. So for now, the next three months because I still feel good, we will try the two of them together and check an MRI. If the MRI is good, we hold and keep doing what we are. If it's not good, let's nuke it. As it stands I am still getting better.

There is no more danger in doing it twice so if I need to I will. I still felt better on chemo than a RAB drug ever made me feel.

No bad vibes here...yet lol

that makes me feel better mate for sure.

i guess the moral is NO ONE KNOWS.

keep on trucking pal.

.

Actually Bob they were not all that surprised. The lesion I have Bob is itty bitty teeny weeny little thing. Compared to the stuff I used to get it still is a HUGE win.

Right now we need to see if it goes away on it's own or not. Does it get bigger in 3 months? Do I get worse? I mean right now my legs feel old as hell, and my right hand still cramps from typing, but I'm getting stronger muscle wise. Neurologically it is going slow, like it did when I got worse.

I've said it 100 times, if it was safe, I would do this once per year if I had too.

That is such great news, Chris and Jamie. Just finished my round of MRI's today. I was thinking of all you guys while I was in the machine. So, I will post when I know the results. The spasticity is killing me, though.

Sandy