{"id":11015,"date":"2014-12-23T10:38:28","date_gmt":"2014-12-23T10:38:28","guid":{"rendered":"http:\/\/carme.dk\/haei\/?page_id=11015"},"modified":"2020-10-13T08:49:39","modified_gmt":"2020-10-13T08:49:39","slug":"hae","status":"publish","type":"page","link":"https:\/\/haeaustralasia.org.au\/","title":{"rendered":"HAE Australasia"},"content":{"rendered":"

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Welcome to HAE Australasia<\/h1>\n

HAE Australasia is a not for profit patient advocacy organisation, dedicated to providing support to Australian and New Zealand HAE patients and their families, as well as raising awareness of hereditary angioedema resulting from C1-inhibitor deficiency. HAE Australasia has been founded by HAE patients and HAE patient caregivers.<\/p>\n

At HAE Australasia, HAE stands for more than Hereditary Angioedema;<\/p>\n