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Board index » Treatments » Revimmune (cyclophosphamide or cytoxan)

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chrishasms
 Post subject: Chris' update
PostPosted: Wed Jun 18, 2008 10:21 pm 
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I got one up on my site.
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mrhodes40
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PostPosted: Fri Jun 20, 2008 3:32 pm 
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Great Chris! I am really happy for you!
marie
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gwa
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PostPosted: Fri Jun 20, 2008 3:51 pm 
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What a turnaround for you! I am very happy for you and your wife.

gwa
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chrishasms
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PostPosted: Sun Jun 22, 2008 12:20 pm 
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My wife just got done doing some MRI comparison stuff you all (especially Bob lol) will love over on my site. Nothing against the folk here it's just that the pics are over there.
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cheerleader
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PostPosted: Sun Jun 22, 2008 1:10 pm 
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WHOA! Chris, your brain doesn't glow in the dark anymore!!!
Praise God, praise Revimmune...what an amazing turnaround for you.
Thanks for posting the pics, Chenelle.
congrats!
AC

_________________
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
dual stents placed 5/09
CCSVI in MS


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Lyon
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PostPosted: Sun Jun 22, 2008 6:47 pm 
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.


Last edited by Lyon on Mon Nov 28, 2011 2:28 pm, edited 1 time in total.

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Jamie
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PostPosted: Mon Jun 23, 2008 7:47 am 
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Thanks Chris.

I'll do the same mid August, do you think Chenelle would do the layout like yours for me?

We've got the pre-HiCy MRI's, I should get the new ones end of July, I'll want to hear what Drs Kerr & Hammond say about them prior to posting.

I'll email Chenelle closer to the time.

Cheers dude.

Jamie.
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MaggieMae
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PostPosted: Mon Aug 17, 2009 10:53 am 
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Chris,

With all the talk about CCSVI, we haven't heard from you (seems like since June) lately regarding how you are feeling post Revimmune. Any new changes for the better?
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chrishasms
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PostPosted: Mon Aug 17, 2009 10:55 am 
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No nothing new to report really. I do feel like the disease progression has been slowed dramatically.

The more I watch this CCSVI stuff the more its making sense to me and some other doctors.
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Board index » Treatments » Revimmune (cyclophosphamide or cytoxan)

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