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.
HAE Patient Identification Card,
click here for details on how to get yours!

The US Hereditary Angioedema Assoc.
Seven Waterfront Plaza
500 Ala Moana Blvd., Suite 400
Honolulu, HI 96813

Toll Free Business Phone: (866) 798-5598
Fax: (508) 437-0303

For urgent assistance, please call:
Donna Davis (808) 216-1029 or
Michelle Williamson (972) 814-5205

Cinryze, ViroPharma's C1-Inh product, is FDA approved and can be prescribed to prevent HAE attacks

Please contact the HAEA's Patient Services group for more information.



Read the highlights of the 2008 National Patient Conference

Clinical Trials
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.

HAE Guide
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.

June 4, 2009 - Read abstracts of HAEA-sponsored research presented May 21-23 in Budapest, Hungary at the 2009 C1 Inhibitor Deficiency Workshop

HAEA.org wins the 2009 AAAAI Distinguished Layperson Award....more
April 2009 Read our SPRING 2009 NEWSLETTER.

March 2009 Watch news coverage on how Cinryze is transforming an HAE patient's life.

Dec. 1 - Discovery Health channel will devote an episode of their program MYSTERY DIAGNOSIS to the story of one of our patients, Janet Long. ...more

May 2, 2008 The latest on C1-Inh approval in the US



Jun 08, 2009 - Dyax Announces FDA Accepts for Review the Complete Response Submission for DX-88 in Hereditary Angioedema

Jun 04, 2009 - VIROPHARMA RECEIVES COMPLETE RESPONSE LETTER FOR CINRYZE™ SUPPLEMENTAL BIOLOGICS LICENSE APPLICATION FOR ACUTE TREATMENT OF HERE

Mar 26, 2009 - Dyax Says FDA Seek More Details On DX-88

Mar 15, 2009 - Rapid Treatment of Hereditary Angioedema Attacks at the Onset of Prodromal Symptoms Decreases Morbidity and Mortality

Feb 04, 2009 - FDA Advisory Committee Favors Approval of DX-88 for Acute Attacks of Hereditary Angioedema

Feb 03, 2009 - FDA cites allergic reactions with Dyax drug



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© 2007-2008 www.haea.org. All rights reserved.
HAEA.org is supported by grants from the following biotechnology companies:
CSL Behring, Dyax Corporation, Genzyme Corporation, Jerini AG, ViroPharma, and Pharming NV