Message for All Current Tysabri Patients
Posted: Wed Jan 31, 2007 3:23 pm
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.
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
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.
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