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.

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Useful links

Find more information about HAE, discussion boards, and support groups for people who live with HAE by visiting the Web sites of several supportive organizations. Use our useful links to learn more about HAE