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ThisIsMS.com :: View topic - News from Opexa
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News from Opexa
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NHE
Volunteer Moderator


Joined: Nov 21, 2004
Posts: 757

PostPosted: Sun Aug 24, 2008 8:37 pm    Post subject: Re: News from Opexa Reply with quote

av8rgirl wrote:
I also have Reynaud's. Just one autoimmune disorder after another!

I started having problems with Raynaud's syndrome about 2 years ago. The distal half of my fingers would go pale and numb. This would occur about every 2 - 3 weeks or so and usually just one finger each time. What's interesting is that about 6 months ago I started taking a combined calcium, magnesium, zinc, and vitamin D3 supplement and I have yet to have a reoccurrence of the Raynaud's syndrome! While I don't know for certain that the supplement is having a causal effect on the Raynaud's symptoms I was experiencing, perhaps a similar supplement could help you out as well?

NHE
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TWG
Family Member


Joined: Jul 09, 2007
Posts: 52

PostPosted: Wed Sep 03, 2008 7:40 am    Post subject: Reply with quote

Opexa found a new partner in research. Check out:

http://www.businesswire.com/portal/site/opexa/?ndmViewId=news_view&newsId=20080903005324&newsLang=en
_________________
Diagnosed with MS in Feb. 14 2000. One of the OLTERMS trial guinea pigs.
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Lars
Family Elder


Joined: Mar 22, 2007
Posts: 273
Location: Durango, Co

PostPosted: Wed Sep 03, 2008 9:11 am    Post subject: Reply with quote

TWG,
You are like a Stealth bomber, occasionally slipping in under the radar to deliver a strike. I can't think of a better connection for Opexa. MRF has been on my favorites list for a long time. I think they have some amazing minds and deep pockets. Thanks for the post. How are you? News on vaccine date?
Lars
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