Haei.org
HAE International (HAEi)
HAE International connects people affected by hereditary angioedema, offering support, resources, and advocacy for this rare genetic condition worldwide.
Support and resources for living with HAE
HAE International (HAEi) is a global nonprofit network dedicated to people affected by hereditary angioedema (HAE), a rare and potentially life-threatening condition. On the site, you can find clear information about HAE, its symptoms, treatments, and how it is diagnosed. There are also resources for family testing, clinical trials, and answers to common questions.
The website offers a supportive community where you can connect with others, find advocacy programs, and learn about regional events or initiatives. Whether you’re newly diagnosed, a caregiver, or just looking for guidance, HAEi provides helpful tools, news, and connections to local patient associations. It’s a welcoming place for anyone seeking understanding and support for living with HAE.
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