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WELCOME

If you or someone in your family has HAE, this site can help with tips on managing this rare disease. It also offers you the opportunity to reach out to others in the "HAE Community" so you can share your thoughts and experiences, use personalized, interactive tools, and learn from others about this rare--but treatable--condition.

CSL Behring Submits NDS to Health Canada Requesting Approval of C1-Esterase Inhibitor for the Treatment of Hereditary Angioedema

5/13/2008

New C1-esterase Inhibitor Highly Effective in Hereditary Angioedema

4/3/2008

C1-Esterase Inhibitor Concentrate Rapidly Relieves Abdominal and Facial Attacks in Patients with Hereditary Angioedema, According to Pivotal Study

3/25/2008

CSL Behring Submits Application to FDA for HAE Treatment

3/6/2008

Read All News >


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ABOUT HEREDITARY ANGIOEDEMA (HAE)

HAE is a rare disease that can cause considerable swelling in various body tissues. A person with HAE will have the disease for life, because it is part of their genetic makeup. However, depending on the severity of the disease, some people will have many attacks each month, while others could go months or even years without a swelling attack.

Unexplained swelling in your hands, feet, arms, legs, face or throat? Unexplained abdominal pain?

Learn more about the symptoms of HAE

Learn more about understanding and living with HAE.

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Find answers to frequently asked questions or pose your own questions to our experts.

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Discover how HAE occurs in families. Track HAE in your family with the Family Tree Builder tool.

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Read other families’ stories about HAE and share your own.

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Keep tabs on symptoms, schedule doctor appointments, and track your medications with our interactive Diary/Journal.

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Last Modified Date: 5/13/2008