Chris' update

A board to discuss Revimmune as a potential therapy for multiple sclerosis
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chrishasms
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Chris' update

Post by chrishasms » Wed Jun 18, 2008 9:21 pm

I got one up on my site.

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mrhodes40
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Post by mrhodes40 » Fri Jun 20, 2008 2:32 pm

Great Chris! I am really happy for you!
marie

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gwa
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Post by gwa » Fri Jun 20, 2008 2:51 pm

What a turnaround for you! I am very happy for you and your wife.

gwa

chrishasms
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Post by chrishasms » Sun Jun 22, 2008 11:20 am

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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Post by cheerleader » Sun Jun 22, 2008 12:10 pm

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
http://ccsviinms.blogspot.com

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Post by Lyon » Sun Jun 22, 2008 5:47 pm

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

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Jamie
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Post by Jamie » Mon Jun 23, 2008 6:47 am

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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Post by MaggieMae » Mon Aug 17, 2009 9:53 am

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?

chrishasms
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Post by chrishasms » Mon Aug 17, 2009 9:55 am

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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