Hi friends and family,
Welcome to Team Kendall! Please take some time to look around the site. We have provided information about Friedreich's Ataxia, Kendall's personal journey, events that you can participate in and ways that you can help. Your support means more to us than you will ever know. If you ever have any questions, please let us know. There are many ways to get in touch with us, including: comments on blog posts, private messages and Facebook.
Talk to you soon,