2021 International Virtual Walk & Roll to Cure FSHD

Team Mighty Max

 

Join My Team!

I watched my Mom and Grandma struggle with this disease, and I don’t want that to happen to anyone, anywhere, ever again. That's why I launched Team Might Max again this year for the Walk & Roll to Cure FSHD.

The money we're raising by participating in this Walk & Roll is supporting programs and funding research that will directly impact patients and their families living with FSH Muscular Dystrophy (FSHD). Facioscapulohumeral muscular dystrophy, or FSHD, is a genetic disorder that leads to the weakening of skeletal muscles. It affects an estimated 1 in 8,000 individuals, or 870,000 people worldwide. Around 20 percent will need a wheelchair by age 50. Over 70 percent experience debilitating pain and fatigue. 

There is no effective treatment or cure, yet... but there is hope.

You can join me as a team member, set up your own personal fundraising page, then invite your family and friends to support you as we march towards a cure. As a participant and fundraiser, you're eligible for lots of great rewards.

Or, you can make a donation to support my efforts! Either way, thank you for your support!


Team Mighty Max