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 Leader

2017 HAEA Supporter

2017 HAEA Friend

 

 

2017 HAEA Research Contributor

 

Jump to our sections with comprehensive content and learn more

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What is HAE

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

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Professionals

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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Resources

Our area with a lot of usefull information

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