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We are MARCHING FOR MARTY on Sunday, April 15th at Heather Farms in Walnut Creek.
It’s hard to believe that my mom has been living with MS for 30 years! And it still has not stolen her incredible spirit (or her naughty sense of humor). And despite the tremendous progress in MS research, there still is not a single treatment for my mom. But we keep saying, “There isn’t a treatment for Mom, YET.” We are determined to do WHATEVER IT TAKES to support all the amazing doctors and researchers who are working tirelessly to find treatments for Progressive MS.
That’s why my mom, Dad, Jamie, Sydney, Tom and I -- along with a bunch of our amazing family and friends -- are creating a “classy, sassy, and a little bad-assy” Walk MS fundraising team! We are going to go out there, have a ton of FUN, and raise as much money as we can.
We hope you will JOIN OUR TEAM, walk, laugh, have fun, and help us raise money so no one will ever have to worry about MS again! The more the merrier!
When you make a donation, you are changing the world for people affected by MS. Symptoms of MS range from numbness and tingling to blindness and paralysis. The progress, severity and specific symptoms of MS in any one person cannot yet be predicted, but advances in research and treatment are leading to better understanding and moving us closer to a world free of MS. Most people with MS are diagnosed between the ages of 20 and 50, with at least two to three times more women than men being diagnosed with the disease. MS affects more than 2.3 million worldwide, and there is not yet a cure. Every dollar raised matters to those affected by MS. Thank you for your support.
Want to join our team?
We’d love to have you. Come walk with us and share in an experience that will change lives—including your own.