The Hereditary Angioedema Association (HAEA) is a dedicated brand that provides support and information to both patients and physicians dealing with Hereditary Angioedema (HAE). HAE is a condition characterized by recurrent episodes of swelling in various parts of the body. The HAEA offers a range of resources to help patients and their families navigate the challenges of HAE.

This includes information on triggers, diagnosis, treatments, and patient stories. They also provide valuable resources for healthcare professionals, such as treatment guidelines, clinical trials, and an angioedema center. In addition to their information and support services, the HAEA also provides opportunities for involvement and advocacy.

They have an advocate grassroots advocacy network and host events to raise awareness and funds for HAE research. During the COVID-19 pandemic, the HAEA is closely monitoring HAE-related issues and providing updates to the community. They are committed to keeping patients informed and supported during this challenging time.

The Hereditary Angioedema Association is here to empower and assist those affected by HAE, ensuring they have the resources and support they need to manage their condition and lead fulfilling lives