Jazmyne and her family are painfully aware of the lack of funding for Friedreich’s ataxia research. As a result, they are passionately fighting to secure any donations to help the tens of thousands of people in the United States suffering from the disease. The following videos provide a personal look into the foundation
September 2018 Emily talks about living with FA
Aug. 2018 – Dr. Payne talks about FA and the growing momentum toward effective treatment
Indy Star – June 10, 2018 Jazz Kitchen Fundraising Event
Dad on a mission to help those with rare disease
2015 Walk For Those Who Can’t
Two Families Receive Life-Changing Gifts from Safe Step Walk-In Tub. Co.