About the Hereditary Angioedema Association (HAEA)
The
United States Hereditary Angioedema Association is a nonprofit patient advocacy
organization dedicated to expediting U.S. approval of safer and more effective hereditary
angioedema (HAE) therapies. In addition to its advocacy work, the HAEA
provides a wide range of services that include clinical trial placement, physician
referrals, education, and individualized patient case management.