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HAE – Australasia
Welcome to HAE Australasia 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. At HAE Australasia,
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HELP RAISE AWARENESS STEP BY STEP We are excited to celebrate the 10th anniversary of hae day :-) in 2021! Starting in April, our activity campaign for this year was to step around the world in time for the 10th anniversary of hae day :-) on 16 May – and we
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We are focused on the development of precision genetic medicines to treat rare neuromuscular and central nervous system diseases. Learn more about Sarepta.
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FAGE is a Greek recipe strained yogurt, with a rich creamy texture and a delicious taste. The possibilities are as endless as your imagination. Good things start here
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FAGE is a Greek recipe strained yoghurt, with a rich creamy texture and a delicious taste. The possibilities are as endless as your imagination. Good things start here
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We are focused on the development of precision genetic medicines to treat rare neuromuscular and central nervous system diseases. Learn more about Sarepta.
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