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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
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
Click on the title above for more information.
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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.
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