US HAEA Core Donors

Thank You To Our Donors!


The US Hereditary Angioedema Association (HAEA) is a non-profit 501(c)(3) patient advocacy and research organization with greater than almost two decades of experience providing the HAE patient community with a wide range of services. The continued generosity of our donors enables the HAEA to provide an expansive array of individualized patient services, educational programs, advocacy, engagement activities and advance groundbreaking research.

2017 HAEA Presidents Circle

2017 HAEA Leader

2017 HAEA Supporter



2017 HAEA Research Contributor


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What is HAE

Get to know the disease: symptoms, diagnose, treatments and more

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For healthcare providers. Knowledge, CME-programs and more

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Living with HAE

Care takers and givers: HAE will affect your life - But you can still be in control.

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Our area with a lot of usefull information

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