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Thank you to our premier national sponsors

Thank you to our local sponsors

If you are interested in sponsoring the 2016 Bike MS: The Road Divided, please contact Sarah Flowers for details.

For our participants and volunteers living with MS.

I Ride with MS

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People who ride in Bike MS may do so to support family members, friends or co-workers who have been diagnosed with multiple sclerosis. But, there are also legions of participants who live, and ride, with the disease, despite challenges such as fatigue or weakness. I Ride with MS is a special Society program that recognizes Bike MS cyclists who are also living with multiple sclerosis.

Anyone living with MS who is interested in cycling to support Bike MS can join the program, enjoy special day-of-event benefits, and receive a complimentary "I Ride with MS" jersey. Genzyme and MS One to One and Primal Wear are proud supporters of the I Ride with MS program, available through all 100 Bike MS events nationwide.

I Ride with MS participants are not only committed to cycling to create a world free of MS, but to increasing awareness. For more information or to add "I Ride with MS" to your registration (if you did not when signing up), please contact the Fundraising Support Center at FundraisingSupport@nmss.org or by calling 855-372-1331.

"I Ride with MS" Stories

Todd Frauendorfer: Growing His Commitment

Todd Frauendorfer

"For me, Bike MS is such a healthy weekend in that you combine the physical part of biking with the emotional aspect that comes with seeing all of the supporters that come out for the weekend," says Frauendorfer, who was met by fellow riders including his wife Linda and teammates at the finish line. "There's a great sense of community and accomplishment since we are all working towards the common goal of ending MS."

"Bike MS gives me a great opportunity to raise awareness, educate others, encourage those who are also diagnosed, and raise money to support the programs that improve the lives of those living with the disease," explains Frauendorfer. "In the past three years, it is amazing the number of people we have encountered that are living with MS or have close friends or family that have been impacted by MS. Participating in the Bike MS event is one way that I can actually feel like I'm doing something about MS rather than just living with it."

Nancy Dressel: Crankin' for a Cure

Nancy Dresser and her grandchildren

Nancy Dressel always finds a way to give to the MS movement, whether she's raising money by selling her hand-sewn aprons at a farmer's market near her home in Port Orchard, Wash.; riding a recumbent bicycle to lead her Bike MS team, Crankin' for a Cure; or, connecting with people to spread awareness about MS.

"I'm loud," says Nancy, who was diagnosed in 1990 at age 35. "I'm not shy. I want to be out in the fun. I want to talk to people." Which is why Bike MS is such a great fit for her. "The riders just blow me away," she explains. "They're out there cranking 150 miles and before that, they're knocking on people's doors for donations, and some of them don't even know anyone with MS. I've had grown men get down on their knees to face me on my recumbent bike and say, 'tell me your story.' It chokes me up."

For Nancy, Bike MS is perhaps most of all a way to connect with the community. "I use the words 'warm and fuzzy' when talking about my neurologist because you've got be able to talk about everything with a neurologist. Well, the experience of Bike MS is also warm and fuzzy. I felt that immediately—the riders just accepted me right away into the fold."

Fontella Addo: Start from Where You Are

Fontella Addo handstand on wheelchair

Fontella Addo remembers her first experience with the National Multiple Sclerosis Society when she was going through yet another of what had become an annual MS exacerbation. "A woman from the Society helped me to get my first wheelchair," she says. "I had to accept that I needed a chair at the time of the exacerbation and I couldn't afford it. She made phone calls and did everything she could to help."

Fontella continued to use services that the Society offered, but hadn't considered Bike MS as a way to give back until a coworker found out she had MS and asked her to join his team, The Spokesmen. "When he found out, oh man, he pushed, pushed, pushed," Fontella, who lives in Leominster, Mass., remembers. "I was like, I will do anything to help, but I haven't ridden a bike since I was 10." But he didn't give up. "He kept pushing, so I finally joined the team and that was that."

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Every ride; every rider; every contribution matters.

Ride with MS

Every day we come one step closer to our goal – a world free of MS. Every day we learn more about the disease and push for new treatments and programs to help people living with MS. None of it would be possible without the vital funds raised through Bike MS.

Since Bike MS was started over 30 years ago, participants, donors, and sponsors have raised over $1 billion dollars to fund MS research and critical programs for people affected by MS.

Fueling Progress for People Living with MS

Collectively, Bike MS and other fundraising efforts have helped accelerate research breakthroughs that change lives and will end MS forever.

  • There are more therapies specifically approved for treating and managing MS, and there are more potential MS therapies in development today than at any other time in history
  • MS is more quickly diagnosed, enabling early and sustained therapy to slow disease activity
  • There is much greater awareness of the many symptoms of MS and ways to address them to improve quality of life
  • Scientists are making breakthroughs in identifying risk factors that can increase a person's susceptibility to MS, which will help reveal new ways to prevent the disease

In addition, we ensure each person living with MS can live their best life with more connections to information, resources, and other people with shared experiences; and that the voices of people living with MS are heard and drive change wherever it is needed.

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