HAE Australasia is a not-for-profit patient advocacy organisation dedicated to serving persons with hereditary angioedema, in Australia and New Zealand. Our goals are highlighted in our name HAE, hope, advocacy and education.
The movement focuses on increasing HAE awareness and education, diagnosis, improving patient access to therapy and fostering research.
The hereditary angioedema community is small and spread across two large countries. Many of us live in isolated areas where medical facilities are limited. We wish to build a community of support for patients with HAE.