?

Description

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.

Website

www.haeaustralasia.org.au

Facebook

www.facebook.com/HAEAustralasia

www.facebook.com/groups/269047199786460

Ages

Child / Tamariki, Youth / Rangatahi, Adult / Pakeke

How do I access this service?

Contact us

Services Provided

Advocacy
Information & support

Region

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
Australia

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