This is the place to find interviews with real people who are facing relapsing MS—and doing so with the help of TYSABRI.
Hear a TYSABRI Fighter and a neurologist talk about the importance of the doctor-patient relationship.
Watch a neurologist and a group of fighters discuss long-term treatment with TYSABRI.
Learn how Bryan Bickell and his family maintain a positive attitude throughout their fight.
Watch as TYSABRI fighters describe how they came to terms with their diagnosis.
Check in with retired hockey pro Bryan Bickell and his family 2 years after his diagnosis.
Hear what it means to Amanda Bickell to support her husband Bryan as his care partner.
Watch former hockey player Bryan Bickell share the lessons he learned on the ice that have helped him in his fight.
Hear how Keith's diagnosis impacted his relationship with his wife Liz, and why their bond is as strong as ever.
Watch Jessica tell the story of how her relapsing MS diagnosis helped her discover her inner fighter.
See how Rick learned to be open with his family about his relapsing MS, even when it scared him.
Watch a group of fighters explain why, for them, the benefits of TYSABRI outweigh the risks.
Hear a group of fighters explain why they chose TYSABRI as their first treatment.
Find out how Bryan Bickell passes the time during his TYSABRI infusions.
Discover how your infusion center can become a community all its own.
Learn about the atmosphere at the infusion center from Heidi and her healthcare team.
Hear Courtney describe how she made the decistion to start TYSABRI by putting facts over fear.
Watch a neurologist and a group of fighters discuss long-term treatment with TYSABRI.
Learn how Bryan Bickell and his family maintain a positive attitude throughout their fight.
Watch as TYSABRI fighters describe how they came to terms with their diagnosis.
Find out how Stacy developed the confidence to speak for herself.
Watch 2 TYSABRI Fighters describe how they use knowledge to conquer fear.