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A board to discuss Revimmune as a potential therapy for multiple sclerosis

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Postby chrishasms » Wed Nov 28, 2007 9:31 am

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Postby Loobie » Wed Nov 28, 2007 9:47 am

Dude!,

Man keep us posted as I know you will. This sounds very promising and also very scary at the same time. I wish you all the luck in the world. This sounds pretty radical, but is also a giant departure from anything else that is being tried so what the hell! I guess I need to read this entire thread, but are you saying you are getting a "new" immune system? Well I'm picking myself up off the floor. If you are running again, I want the info! I miss running soooo much. Not much else for me to say except good luck again and you know we are all pulling for you.

Lew
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Postby Loriyas » Wed Nov 28, 2007 9:48 am

Oh Chris, how exciting for you. I wish you all the best. Please keep us posted as to how you are doing.

Best of luck!
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Postby chrishasms » Wed Nov 28, 2007 9:51 am

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Postby MaggieMae » Wed Nov 28, 2007 10:14 am

Chris,

This is what I wanted to hear. I'm so excited for you. I hope everything goes great. When I read about this treatment and first mentioned it on the Tovaxin forum, I was hoping that someone who was involved in the treatment would post. Then came the posts from HiCy and now you will be able to tell us first-hand about your experiences.

It seems that you are so much more hopeful than you were in your previous comments about Revimmune. Apparently you have talked to someone personally at John Hopkins.

My husband said he would try anything rather than continue to go "downhill" with MS and I know others who are even worse off than my husband and they are ready to give up. So, keep us informed.
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Postby chrishasms » Wed Nov 28, 2007 11:27 am

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Postby Rudi » Wed Nov 28, 2007 11:42 am

Wow this is very interesting. Good luck.
1st traceable symptoms July 2006 - realized I had MS November 2006
CAP since 27/04/2007. Various supplements and dietary modifications.
Male 27 UK
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Postby flipflopper » Thu Nov 29, 2007 10:40 am

I find this treatment interesting. If I don't have good results with Tovaxin, if I qualified for this trial and if a site opened near where I live, I would look into this study.


Best of luck to you Chris!
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Postby Sharon » Thu Nov 29, 2007 12:19 pm

Good luck Chris!

Now for the real information you want to hear. The endpoint is to improve, so if you do not improve, you will definitely know the disease activity is done nevertheless. Everyone however is showing improvement. Everyone that my contact has seen.


I am curious - what is the improvement being shown? Does the improvement include repair to the nervous system?

Hopefully, you will have enough good days during your treatment that you can strap on your WalkAide and play tourist.

Take care,
Sharonl
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Postby chrishasms » Thu Nov 29, 2007 12:44 pm

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Postby Lyon » Thu Nov 29, 2007 1:08 pm

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Postby CureOrBust » Thu Nov 29, 2007 11:31 pm

chrishasms wrote:This gets all the MRTC's. Not just the ones they know about.
Does this (& Tovaxin for that matter) only remove (to the current best of knowledge) stuff (i.e. MRTC's) from the blood (or items at any point in the peripheral blood stream)?
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Postby Lyon » Fri Nov 30, 2007 6:03 am

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Postby chrishasms » Fri Nov 30, 2007 6:54 am

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Postby chrishasms » Fri Nov 30, 2007 11:57 am

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