Hi legz,

I think you are such a 'UP" person. I hope your Neuro finds the right medication for you. Maybe it's time to revisit the tx options. I wish you good luck at your next appointment.

This was a site I read many times. It makes me feel better.

You Are Not Your MRI

Don't Feel Doomed ~ ~
MRI applies only indirectly. You may benefit eventually from new research, but that's a slow process. More likely, your neurologist may use MRI to assess whether your treatment is helping you adequately.

Accordingly, your neurologist may be motivated in part by your MRI to make changes in your treatment. But it's the clinical picture-how you function when examined (your eyes, strength, balance, and so on)-that speaks 1,000 words. As Randall Schapiro, MD, has publicly said, "You have to treat the person, not the MRI."

http://www.mult-sclerosis.org/news/A...otYourMRI.html