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The Australasian Lymphology Association (ALA) is the peak professional organisation for the promotion of best practice in the lymphoedema management, research and education.
The ALA provides public listing of accredited lymphoedema practitioners and lymphoedema information to health professionals and people living with lymphoedema.
The ALA is a not-for-profit voluntary organisation which promotes awareness of lymphoedema and advocates for improved services and resources for people living with lymphoedema.
The ALA has charity status for a lymphoedema research fund.
Last reviewed: July 2019
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Read more on Australasian Lymphology Association website
Read more on Australasian Lymphology Association website
The aims of lymphoedema treatment are to prevent progression of the condition, to reduce odema and then maintain the improvement.
Read more on Australasian Lymphology Association website
Read more on Australasian Lymphology Association website
Lymphoedema is the accumulation of excessive amounts of protein-rich fluid resulting in swelling of one or more regions of the body.
Read more on Australasian Lymphology Association website
The National Disability Insurance Scheme (NDIS) provides individualised support for people with disability, as well as their families and carers.
Read more on Australasian Lymphology Association website
Read more on Australasian Lymphology Association website
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