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
Jumpin’ for Jazz
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.