Welcome to the U.S. Hereditary Angioedema Association's website. We are a non-profit patient advocacy organization dedicated to expediting US approval of safer and more effective HAE therapies. In addition, we provide a wide range of services that include clinical trial placement, physician referrals, education, and individualized patient case management. Please click here and fill out a short form so we can provide you with the latest information regarding new HAE treatments and events sponsored by the HAE Association.
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  Bring much-needed HAE treatment to the US. Sign up to participate in the clinical trials  Register to be a member of our message forum and be a part of the HAEA online community.Frequently Asked Questions About HAE Everything you need to know about HAE diagnosis and treatment Angioedema Table Find out the difference between the different types of Angioedema New Treatment Options Learn about the ongoing clinical trials which will revolutionize the way HAE attacks are treated. Physician Referral Find a physician near you. HAE Patient Email Support Group Reach out to other HAE patients by subscribing to our message forum Be part of our Volunteer Network! Join our network of HAE patients who are motivated to help serve our patient community. |
 Apr 15, 2008 - Lev Takes Steps to Bring Cinryze to Market for the Treatment of HAE Mar 18, 2008 - AAAAI: New Therapies on Horizon for Angioedema Attacks Mar 18, 2008 - FDA Advisory Committee to Review Cinryze HAEA News
October 2007 - Highlights from the 2007 HAEA Patient National Conference in St.Louis, MO March 2007 - Read our March Newsletter eBay users, here's a new way to give!  Buy or sell on eBay and support HAEA.com. |
