TYSABRI fighter’s forum videos
This is the place to find interviews with real people who are facing relapsing MS—and doing so with the help of TYSABRI. Learn a bit about how they fight—and why they fight.
Feel free to watch these clips as often as you like. And be sure to sign up for future updates on TYSABRI.
"To have that never-give-up attitude is the wisdom of, really, my life.”
“He goes through a lot of emotions that anyone would. We talk about that a lot. We don’t just play it off as if it’s nothing."
"A big thing in any sport is to be positive. Negativity rubs off on teammates or rubs off on your game. When I got diagnosed, being positive was a huge thing me and my wife wanted to do. It helped me get through it."
“Keith has inspired me in the way that he has taken something so terrible, something that’s so life-changing and has chosen, on a daily basis, to continue.”
"Though MS took so many things away from me, what I’ve taken from MS is a strength and a courage that I never knew."
"My condition made me realize that I don't fight for myself. I fight for my family."
“We still do talk about the risk vs benefit, but for me, the benefit outweighs the risk.”
"We know that with MS, the sooner you get on treatment, the better the long-term outcomes are going to be."
“When I have to go for my treatment, I can break up my everyday routine. I’ll watch TV—usually highlights—or take a nap.”
"The infusion center can become a little community; patients start requesting times or getting each other’s phone numbers and start to meet up outside of their treatment time."
“When I come to the center for my infusion, it’s two hours. The first hour, I get my medication. The second hour, they observe me... Most of the time I interact with the other patients. It’s fun to catch up with them.”
“It was very important to me to make my decision based on facts instead of fear.”
“When I go in for my infusions, my doctor will schedule recently diagnosed or new patients at the same time as me.”
"We’re enjoying what we have and what’s in front of us and what’s next."
"When I met my doctor, I told her that I needed to figure out how to make this disease fit into my life."
“I became an advocate for myself. I feel empowered; I feel like it’s the one thing with this disease that I can control.”
"It’s important to communicate what you feel is best for you and what you want and need from your treatment."
“Your doctor knows you, but he doesn’t know what you’re thinking or what you need unless you tell him.”