Jon Davis has been involved with the Bleeding Disorders Association of the Southern Tier, Inc. (BDAST) since 1996 after his infant son was diagnosed with severe hemophilia A at age six months. In 1998, his second son was diagnosed with severe hemophilia A at birth. Jon joined the BDRN Team in May 2009. He enjoys working with a team of professionals who have vast experience, expertise and compassion in helping individuals and families manage their bleeding disorders. He currently serves as president of the Bleeding Disorders Association of the Southern Tier, a member organization of the Hemophilia Federation of America. He is also a member of the New York State Hemophilia Advocacy Coalition and National Hemophilia Foundation. Jon lives with his wife Lynda and two sons in Upstate New York.