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Board index » Treatments » Revimmune (cyclophosphamide or cytoxan)

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sh8un
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PostPosted: Sun Feb 24, 2008 9:48 am 
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Joined: Wed May 03, 2006 3:00 pm
Posts: 303
Location: Calgary, AB, Canada
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
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chrishasms
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PostPosted: Mon Feb 25, 2008 6:48 am 
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Joined: Thu Sep 14, 2006 3:00 pm
Posts: 1161
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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Lyon
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PostPosted: Mon Feb 25, 2008 7:48 am 
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Last edited by Lyon on Tue Nov 29, 2011 7:02 pm, edited 1 time in total.

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sandonpoint
 Post subject: Another article.
PostPosted: Sun Mar 09, 2008 4:00 am 
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Joined: Fri Feb 22, 2008 4:00 pm
Posts: 26
Check this one out .

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

Regards

sandon.

Abtract only
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Board index » Treatments » Revimmune (cyclophosphamide or cytoxan)

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