It’s your CHOICE, it’s your voice.
CHOICE (Community Having Opportunity to Influence Care Equity) is a project driven by Hemophilia Federation of America (HFA) and supported by the Centers for Disease Control and Prevention (CDC). CHOICE collects information through an online and paper-based survey. This survey collects information regarding health experiences of people who have a doctor-diagnosed bleeding disorder and do not receive care at a federally-funded hemophilia treatment center (HTC). HFA’s goal for the CHOICE Project is to put the survey results to work to improve the lives of those in the bleeding disorders community.
Take the CHOICE Survey
Ready to take the CHOICE survey? Completing the CHOICE survey should take about 20 minutes. This is time well spent because with more information we have a better chance of learning what we can do to improve the health of people with bleeding disorders. Choose a language:
Preview the CHOICE Survey: Anyone with a bleeding disorder is welcome to take the CHOICE survey, whether or not you receive care at a hemophilia treatment center (HTC). If you want to see the survey before you take it, click to see adult male, adult female, and parent/guardian, surveys in English or las encuestas por hombre adulto, hembra adulta, y los padres en Español.
Aprenda sobre el Proyecto CHOICE.
Learn more about what the CDC is doing in the area of blood disorders at http://www.cdc.gov/ncbddd/blooddisorders/aboutus.html