US Hereditary Angioedema Association

Fairfax City,  VA 
United States
  • Booth: 1443

The US Hereditary Angioedema Association (HAEA) is a non-profit patient advocacy organization, providing a wide range of patient services,
dedicated patient advocates who are themselves HAE patients or caregivers, and clinical research support for this rare genetic blood disease.  We display information on HAE diagnosis, 
treatment, our patient registry, and the US HAEA Angioedema Center at UCSD.

For Technical Support with this webpage, please contact support.