From CEO Fiona Wardman, HAE Australasia HAE Australasia Youth Group is up and running, and the group facilitator Jess has done a great job in connecting some of our youth from Australia and New Zealand. We would encourage more youth to join the group as we have some projects and a competition for them [...]
From CEO Fiona Wardman, HAE Australasia HAE Australasia held its strategy meeting during January 2020. This meeting brings together the HAE Australasia Board of Directors to discuss the projects and initiatives for the coming year. The Board is excited about the new projects the organization will be working on to bring more HAE education and [...]
From CEO Fiona Wardman, HAE Australasia: HAE Australasia has submitted the ethics application to join the Global Registry in Australia. We hope to have a positive answer very soon so we can start rolling out the project around the country. Once again this year, we attended the Australasian Society of Clinical Immunology & Allergy (ASCIA) Conference, where we had the [...]
From CEO Fiona Wardman HAE Australasia has met with the Pharmaceutical Benefits Advisory Committee (PBAC) to provide consumer comments on the funding of one of the new prophylaxis therapies. The presentation to the committee and comments were well received by the panel; however, unfortunately, the government at this time rejected the results of the submission. The panel have recognized that there is [...]
From HAE Australasia CEO Fiona Wardman: During April HAE Australasia held their 2019 HAE Patient & Carers Conference on the Gold Coast, Queensland. This was the first time the conference was held over two days, and also the first time we had separate youngsters sessions. Day 1 opened with an amazing and inspiring keynote speech from Gidon Goodman, who is [...]
HAE Australasia / NEW ZEALAND New Zealand · Australia & Oceania On this page we have pulled together presently available information relevant for HAE patients and caregivers in New Zealand. HAE online in New Zealand Visit [...]
HAE International is a global non-profit network of member organizations dedicated to raising awareness of hereditary angioedema and improving the lives of people with HAE.
HAE International (HAEi)
10560 Main Street, Ste PS40
Fairfax City, VA 22030
United States of America
gro.ieah@ofni
HAE International (HAEi)
Vejlevej 16, 1.
8700 Horsens
Denmark
gro.ieah@ofni
