Connecting with the HAE Community

Learn how others are living well with hereditary angioedema (HAE).

About the HAEA

Learn about the Hereditary Angioedema Association (HAEA), a nonprofit organization dedicated to expediting U.S. approval of safer and more effective HAE therapies.

Useful links

Find more information about HAE, discussion boards, and support groups for people living with HAE by visiting the Web sites of several supportive organizations.