Resources

• HAE Essentials
• Media Library
• Physician Letter
• School Resources
• Patient Toolbox
• Hereditary angioedema with normal C1 inhibitor function: Consensus of an international expert panel
• Patient ID Card
• HAE Medical Glossary
• Bibliography
• HAE International

Media Library

The US HAEA is constantly working to develop a wide range of media resources that communicatehow, in this new era for Hereditary Angioedema, patients can take charge of their HAE.  In 2011, our radio programs reached over 5 million listeners.  Video programs reached millions more.

We provide this HAE information in its various formats for you to share with colleagues, your local community, friends and family.

Tony’s Testimony

US HAEA President, Anthony Castaldo, testifying to the Appropriations subcommittee

HAE Day Benefit Concert

Please stay tuned for more information as planning is finalized.

HAE PSA

Watch a Public Service Announcement (PSA) released to a wide audience about how FDA-approved HAE medications available today mean that HAE patients now have CHOICE.

Many Faces, One Family

Watch this video featuring patient interviews at one of our HAE Conferences.

HAEA Conference

HAE TV Public Service Announcement (PSA)

HAEA Podcast

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Checkout a recent podcast or a radio program produced to raise HAE education and awareness among the general public.

Radio Interview, WESB-AM, Buffalo

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Radio Interview, KFAB-AM Omaha

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Radio Interview, Puerto Rico (in Spanish)

A radio interview with Tony Castaldo, Janet Long, and HAE patients in Puerto Rico to raise HAE awareness.

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Part 1

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Part 2

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Part 3

Radio Interview, Puerto Rico (in Spanish)

HAE Day :) Interview in Puerto Rico (in English)

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Part 1