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Joined: Aug 14, 2006 Posts: 103 Location: So. Calif.
Posted: Wed Jan 31, 2007 5:23 pm Post subject: Message for All Current Tysabri Patients
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 websitewww.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.
If any of you would like to share your 2006-2007 Tysabri experiences on the 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 _________________ Feel free to visit my Blog and leave me a comment, I'd love to hear from you!
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We encourage you to also visit our Multiple Sclerosis story and support community on Experience Project.
Experience Project is a vast and powerful community where people connect anonymously through life experiences. It's made by the same people who built This is MS,
on the premise that no one life experience-- like having MS-- defines a person. It now covers over 2 million life stories. Find and share yours!
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