US Hereditary Angioedema Association

Español

ABOUT HAE
RESOURCES
GET INVOLVED
- Advocate
- Donate
- Fundraise
- Events
- Scientific Registry
- Youth Activities
- Volunteer
- Shop
- Join Us
ABOUT US
NEWS
CONTACT US

HAEA IN ACTION
NEWSLETTER

Filter by:

Pre-2021
Newsletter Archive

The US Hereditary Angioedema Association
10560 Main Street, Suite PS40
Fairfax City, VA 22030

CONTACT AN HAE ADVOCATE: (866) 798-5598

DONATE JOIN HAEA

Use of this site implies your agreement with our Terms of Use / Privacy Policies
The US Hereditary Angioedema Association (HAEA) is a 501(c)(3) non-profit organization.
© 2021 US Hereditary Angioedema Association

The HAEA is an advocacy and research organization committed to actively engaging our community in a wide variety of grassroots activities that promote HAE education and awareness. We provide personalized services to address the unique needs of people with HAE and their families, which includes helping them secure access to and reimbursement for modern HAE medicines. Our great success in supporting clinical research has resulted in a variety of FDA-approved therapeutic options. We work closely with expert physicians to continuously upgrade our community’s quality of life through improving diagnosis and knowledge of the condition, and encourage an individualized approach to selecting an optimal treatment. The HAEA is product and company neutral, and continues to enthusiastically support drug discovery research aimed at the next generation of HAE therapies.