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Discovering you have a rare, lifelong disease that will impact your life may feel daunting.
That’s why HAEA was founded — so people with HAE can learn how to live better, help find a cure, and simply connect with one another to share experiences.
Don’t miss out! Get the latest on HAE therapies, research and events by joining the US HAEA.
Our Patient Services Team understand what it means to live with HAE. Contact a team member in your area.
For patients needing assistance with a diagnosis, the US Hereditary Angioedema Association can help refer you to a physician who is knowledgeable about HAE.