HAE (hereditary angiodema) Australasia is a not-for-profit patient advocacy organisation dedicated to serving persons with hereditary angioedema, in both New Zealand and Australia.

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.




Child / Tamariki, Youth / Rangatahi, Adult / Pakeke

How do I access this service?

Contact us

Services Provided

Advocacy, Information & support, Injury, illness or disability


Bay of Plenty, Canterbury, Central Auckland, Central Lakes, Dunedin - South Otago, East Auckland, Hawkes Bay, Hutt, Lakes, MidCentral, Nelson Marlborough, North Auckland, Northland, South Auckland, South Canterbury, Southland, Tairāwhiti, Taranaki, Waikato, Wairarapa, Waitaki, Wellington, West Auckland, West Coast, Whanganui

Contact Details

Postal Address

PO Box 285, Webb St
Narre Warren
VIC 3805

This page was last updated at 5:23PM on May 10, 2022.