Thread: Tysabri
View Single Post
Old 01-19-2007, 06:44 PM
Chris's Avatar
Chris Chris is offline
Member
 
Join Date: Aug 2006
Location: Georgia
Posts: 975
15 yr Member
Chris Chris is offline
Member
Chris's Avatar
 
Join Date: Aug 2006
Location: Georgia
Posts: 975
15 yr Member
Default

Quote:
Originally Posted by ArmyMahmaa View Post
Good morning.
I am looking for information from anyone with MS that has taken or is taking Tysabri.
I am looking to find out your thoughts and/or experiences with this medication.
I have been on Rebif for 3 years now and still average a relapse 2 to 3 times a year. My doc and I are looking at doing the Tysabri. Before I agree I just wanted to find out as much as I could.
I am aware of the episodes from 2 years ago and understand the happenings that caused them.
I just need information from others about Tysabri.
Before I did 5 infusions of Novantrone, I did not do research or ask others about it. I wish I had. My heart didn't take to kindly to it. I have a low ejection fraction, 3 valves regurgitate, and I have a murmur. All which was not there prior to treatment because of the echo done before.
Any information and advice will be so appreciated.
Thanks
Sheila
Hello Sheila.
I have experience with Tysabri. I was in the original Antegren studies and was on it along with Avonex as it turned out. I can tell you that after the second infusion of what was then called Antegren, I felt fanatastic. I had much more energy than I've had in years, and it was obvious that I wasn't on the placebo. I was in the study for 18 months until it was aborted in order for Tysabri to be marketable to the general public.

At that time, my husband and I decided to try and get pregnant, so I stopped the Avonex, and opted out of taking the Tysabri. I am still here to talk about it as you can see, and I had a most positive experience with it. We are still trying to obtain a viable pregnancy and I am not on it as of now. Should we opt for another way to have children (adoption), I most certainly will begin taking Tysabri again. I am fortunate enough to live near an MS Center where there is a large infusion room. There were and are many Tysabri patients being treated with it that have had many fine results from Tysbri. I'm sure your Neurologist would be happy to put you in touch with another Tysabri patient if you so desire. I have spoken to several in my area through the Center I go to. The physicians I see have a list of patients who have signed up to serve as advocates for those seeking information about Tysabri.

It is a significant decision to make. If you don't like Tysabri, you don't have to stay on it; just as we were allowed to drop out of the Antegren study if we opted. I support you in whatever you do decide to do.

All the best.
Chris
Chris is offline   Reply With QuoteReply With Quote