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 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
sh8un
Family Elder
 
Posts: 303
Joined: Wed May 03, 2006 2:00 pm
Location: Calgary, AB, Canada

Advertisement

Postby chrishasms » Mon Feb 25, 2008 5:48 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.
chrishasms
Family Elder
 
Posts: 1161
Joined: Thu Sep 14, 2006 2:00 pm

Postby Lyon » Mon Feb 25, 2008 6:48 am

.
Last edited by Lyon on Tue Nov 29, 2011 6:02 pm, edited 1 time in total.
Lyon
Family Elder
 
Posts: 6063
Joined: Wed May 03, 2006 2:00 pm

Another article.

Postby sandonpoint » Sun Mar 09, 2008 3:00 am

Check this one out .

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

Regards

sandon.

Abtract only
User avatar
sandonpoint
Family Member
 
Posts: 26
Joined: Fri Feb 22, 2008 3:00 pm

Previous

Return to Revimmune (cyclophosphamide or cytoxan)

 


  • Related topics
    Replies
    Views
    Last post

Who is online

Users browsing this forum: No registered users


Contact us | Terms of Service