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Lymphoedema Registry | Launch - March 2015

A project of the ALA with support of the LAA and state lymphoedema support groups. Analysis of collected data is provided via SPSS by an IBM Community Grant

To achieve a robust data set the ALA, support groups and individual lymphoedema practitioners are asked to promote and encourage every person with lymphoedema to join the registry. The Website: www.lymphoedemaregistry.org.au

2016 Asia Pacific Lymphology Conference | 26-28 May 2016, Darwin

Theme: New Networks - New Solution

Incorporating the 11th Australasian Lymphology Association | Conference and the 6th International Lymphoedema | Framework Conference

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ALA has been awarded an IBM community grant

The ALA has been awarded an IBM community grant providing access to data training and analysis for the proposal for the development of a Lymphoedema Patient Registry. More news to follow.

23/09/2014 | The ALA is now connected to Health Direct

ALA is now proudly, a partner of the HealthDirect government network

Update on ALA partnered research project

The ALA partnered with the BCNA, Smith & Nephew and Macquarie University Cancer Institute in the research project: The socio-economic impact of living with cancer related lymphoedema. Online survey has commenced. Click on the title to read more and participate in the survey

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Have your say, like us on Facebook

Our market review demonstrated that this is one of the fastest growing demographics we can use to raise awareness in lymphoedema. With a simple posting we have tracked the posting and have been able to reach many 100s of people over a wide and international range in a very short time.
Don't be afraid! This is a closely monitored site by the ALA, with links back to relevant evidence based documentation supported by the ALA. So Like our page!
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