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Board index » Treatments » Revimmune (cyclophosphamide or cytoxan)

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MSGREG
PostPosted: Sun May 24, 2009 8:35 am 
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Hello Everyone: Thank you for posting so many positive comments. It always makes me happy to read them and to know there is some hope to at least lessen the effects of this horrible disease.

My questions: where and how much?

I'd really like to take this treament early (I've been diagnosed with RRMS for just over a year now) and I'd really like to know who to contact to (hopefully) get this thing started.

Thanks again everybody. Stay positive.
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pvns2005
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PostPosted: Sun May 24, 2009 5:07 pm 
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Joined: Fri Nov 17, 2006 4:00 pm
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Check you messages. I sent the info there.
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carepear
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PostPosted: Thu Jun 25, 2009 2:19 pm 
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Can you send it to me as well?

I was told only John Hopkins was doing it but it seems like other places are now.

Thanks,
Carolyn
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pvns2005
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PostPosted: Fri Jun 26, 2009 5:15 am 
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carepear,

Check you messages. I sent the info there.
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LR1234
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PostPosted: Thu Jul 09, 2009 5:09 am 
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Location: California
Could someone also send me the details? I am also going to seriously consider this treatment as many of you have had improvements from it.

L x
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rssugg
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PostPosted: Tue Jul 14, 2009 5:35 pm 
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Joined: Mon Jul 06, 2009 3:00 pm
Posts: 104
Is Revimmune still on track? Like the user above, I am fairly new to MS at just over two years. Young professional with a lovin wife and a baby on the way. Id like to learn more about this, but it seems that most all of the folks who did Revimmune last year post very little. Is this treatment still available?
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chrishasms
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PostPosted: Wed Jul 15, 2009 8:09 am 
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Yes it is and the reason we don't post here very often is because we have gotten on with our lives.
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rssugg
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PostPosted: Wed Jul 15, 2009 8:58 am 
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Good good! Getting on with life is a good thing! I'm glad everyone is well. Good luck!
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Board index » Treatments » Revimmune (cyclophosphamide or cytoxan)

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