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The Florida Hemophilia Association, Inc is a Not-for-Profit organization that is dedicated to enhancing the quality of life in the bleeding disorders community by creating programs and services that provide education, emotional support and advocacy. We are contributing toward research to ultimately find a cure.
Created 29 years ago, the Florida Hemophilia Association has become a vital resource and network of support for families and individuals in Florida affected by hemophilia and other bleeding disorders. Throughout its history, FHA has created various educational programs and services that allow those affected to come together and help each other through the tribulations of having a bleeding disorder. Some of our annual programs include: the Family Education Symposium, Mother's Brunch, Holiday Duo family picnic and the Walk in the Jungle. These events not only help raise funds and educate our community on treating and living with bleeding disorders, but they also spread the message about bleeding disorders to the general public, building the awareness level each year.