Useful Links

The following Web sites are excellent sources of information about hereditary angioedema (HAE), for physicians and patients alike:

Other resources for information about HAE

Patient organizations: North America

HAE organizations: international

Disease Web sites

Registration

Register for updated information on HAE disease management.

US Hereditary Angioedema Association (HAEA)

Learn about the HAEA, a non-profit organization that provides a wide range of services, including clinical trial placement, physician referrals, education, and individualized patient case management. Visit HAEA.org