Full text of recent study at Stony Brook .

A board to discuss Revimmune as a potential therapy for multiple sclerosis

Postby sh8un » Sun Feb 24, 2008 9:48 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.
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Postby chrishasms » Mon Feb 25, 2008 6:48 am

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.
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Postby Lyon » Mon Feb 25, 2008 7:48 am

Last edited by Lyon on Tue Nov 29, 2011 7:02 pm, edited 1 time in total.
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Another article.

Postby sandonpoint » Sun Mar 09, 2008 4:00 am

Check this one out .

http://cjns.metapress.com/openurl.asp?g ... &spage=539



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