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.
Vision and mission
Excellence in health care for people living with lymphoedema.
Supporting professionals to promote awareness of, and provide best practice in, the management of lymphoedema.
How the Australasian Lymphology Association can help
The ALA provides a public listing of ALA Accredited Lymphoedema Practitioners and lymphoedema information to health professionals and people living with lymphoedema.
