My name is Kendall Harvey and I live in Austin, Texas. I was diagnosed with Friedreich's Ataxia (FA) in August 2013 at the age of 25. I am now 30, and a mother to two BEAUTIFUL children.
FA is a debilitating, life-shortening, degenerative neuro-muscular genetic disorder. On Team Kendall, our mission is to raise awareness about FA. We aspire be a contributing partner on the journey to find a cure. On March 24th, my team and I will ride with rideTAXIA in Dallas. We'll be joined by several local FA families, friends and cycling enthusiasts riding as a team to redefine what is possible in FA research. Join us in supporting the urgent pace of that research.
We are always looking for new team members, so please sign up to be a part of Team Kendall! If you are unable to participate, help us raise awareness by sharing our story. Donations are also very appreciated. Every penny counts and no donation is too small. Be a part of the journey to find a cure and together we WILL cure FA! - See more at www.teamkendall.org!