
HEREDITARY ANGIOEDEMA ASSOCIATION INC
The US HAEA is a non-profit advocacy and research organization serving people with HAE. #HereditaryAngioedema The US HAEA is a non-profit advocacy and research organization serving people with HAE. To lead a nationwide advocacy movement that focuses on increasing HAE awareness and education, empowering patient access to suitable treatment, and fostering ground-breaking research that includes searching for a cure.

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2005
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- HAEA To lead a nationwide advocacy movement that focuses on increasing HAE awareness and education empowering access to suitable treatment and fostering groundbreaking research that includes searching for a cure. Unrestricted access to therapy so people affected by HAE are unburdened by symptoms and able to experience life to the fullest. To fulfill our communitys highest priority needs with innovative programs services and activities that are delivered with an extraordinary level of empathy kindness and compassion. TAKE ACTION Your contribution helps fund our many programs and resources for people living with HAE and their loved ones Join our efforts to maintain a strong political advocacy presence on Capitol Hill Get involved and help serve our community Participate in one of our many ongoing initiatives or create your own.
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- HEREDITARY ANGIOEDEMA ASSOCIATION INC
- 2025-08-04
⭐ Do you know a young person making a difference in the HAE community. (tw) ... more
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- HEREDITARY ANGIOEDEMA ASSOCIATION INC
- 2025-08-01
🎓 ⭐Applications for Spring 2026 HAEA Scholarships are NOW OPEN. (tw) ... more
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Odpovědí v diskuzi
1
1. How can we improve community outreach and education efforts to raise awareness about Hereditary Angioedema among healthcare providers and the general public?
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Brooklyn Simmons
2 days ago
Odpovědí v diskuzi
1
2. What innovative programs or initiatives could the HAEA implement to better support patients and caregivers in managing the challenges associated with HAE?
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Brooklyn Simmons
2 days ago
Latest reviews
Together, we can make a real impact in communities around the world. Help us bring hope and support.
💙 So proud to support the HAEA in their mission to raise awareness and provide resources for those affected by HAE! Together, we can make a difference! #HereditaryAngioedema

Brooklyn Simmons
Product Manager
🌟 The work the HAEA is doing is truly inspiring! Let's spread the word about HAE and fight for better treatment options for everyone impacted. Join the movement! 💪

Brooklyn Simmons
Product Manager
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Kendall Monroe
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