The Hemophilia Foundation of Greater Florida is a 501c3 nonprofit organization that has supported the bleeding disorder community throughout the state of Florida since our founding in 1996. For over 20 years, we have been helping those living with and affected by bleeding disorders to live without limits through much needed services and programs.
Our mission is to improve the quality of life for people with bleeding disorders and their families through education, information and referral services, advocacy and research.
Board of Directors
The Hemophilia Foundation of Greater Florida Board of Directors are non-compensated volunteers who serve the bleeding disorder community.
Pete Vrochopoulos, President
Mike Berkman, Vice President
Alan Apte, Vice President
Ed Bookbinder, Board Member
Hector L. Cartegena, Board Member
Joe Riggs, Board Member
Eileen Gregory, Board Member
Jose Villareal Charris, Board Member
Fran Haynes, Executive Director
Dina Richardson, Social Worker
Missy Zippel, Education Outreach Nurse
Shannon Baidenmann, Office Administrator
Leanne Buchanan, Education and Outreach Nurse