Posted: Sun Feb 24, 2008 8:48 am
Wow...it is so annoying to know that this stuff has been around since 1967 and yet I never heard about it from my neurologist. I found out about it here.
NN
NN
I hate to say it, but if you are expecting your Neuro to be proactive and take a meal ticket out of their families pocket, it isn't happening.
I go to Dr. Allen Bowling, aka MR. MS in Colorado. He has done nothing proactive only reactive, and he is a great doctor and I would want no one else.
I found Revimmune, as I would bet most of the folk on here in the Tovaxin trial or this treatment found it themselves. Most Neuro's don't care until something is going into Phase III, or being approved.
Sux ass I know.