- ABOUT HAE
- For Healthcare Professionals
- For Caregivers
- ER Toolkit
The US Hereditary Angioedema Association (HAEA) is a 501 (c)(3) non-profit advocacy and research organization committed to actively engaging our community in a wide variety of grassroots activities that promote Hereditary Angioedema (HAE) education and awareness.
Our Media Kit includes organization highlights, HAE facts, program overviews, research accomplishments, downloadable digital assets, and more.