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Board index » Treatments » Tysabri (Antegren or Natalizumab)

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msladyinca
PostPosted: Wed Jan 31, 2007 4:23 pm 
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Joined: Sun Aug 13, 2006 3:00 pm
Posts: 104
Location: So. Calif.
Hi everyone,

As some of you know, I was one of the MS patients that testified (via video) before the FDA AC Hearings on March 7, 2006, in an effort to voice a patient's opinions re: Tysabri and try to bring Tysabri back to those of us who want/need it as an option to fight our disease.

A small group of us formed the all-volunteer non-sponsored website http://www.mspatientsforchoice.org/ that provides accurate and up-to-date information on Tysabri, including spectacular data released at the recent 2006 ECTRIMS Conference, videos, and Tysabri Patient Progress Reports.

Let me say that I am so very happy for each of you that, imho, you now have a superior efficous medication (Tysabri) to help you fight your MS. :D

If any of you would like to share your 2006-2007 Tysabri experiences on the http://www.mspatientsforchoice.org/ website, which will be helping other MS'ers looking for Tysabri information, please send me a PM with your email address, or send me an email directly at LGLBGL2003@AOL.com for further information.

I wish you all success in your Tysabri therapy (symptom improvements whether minor or dramatic, and/or stablization of your MS) with much, much, much happiness and Hope with Tysabri, always.

Take very good care all,

Lauren :P

_________________
Feel free to visit my Blog and leave me a comment, I'd love to hear from you! :)

http://lauren-livingwithms-aolcomlglbgl ... gspot.com/

Co-owner of a MS Support Group
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Board index » Treatments » Tysabri (Antegren or Natalizumab)

All times are UTC - 8 hours [ DST ]

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