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Australasian Lymphology Association has a Facebook page to share and hear the latest news and information on Lymphoedema. Go ahead and like us for more information.

August 2014

The ALA is part of the LYMPHOEDEMA ACTION ALLIANCE

The ALA is part of the LYMPHOEDEMA ACTION ALLIANCE for equitable access to quality lymphoedema services in NSW and to make compression garments accessible via the Medical Benefits Scheme. The Launch of the Action Alliance and online campaign will be in October 2014. More information to come.

August 2014

Webinar - It’s not okay to fly and other myths about lymphoedema.

A new look, based on current research, at advice or guidelines for women who have had treatment for breast cancer and are at risk of developing arm/breast lymphoedema

Date: Tuesday, 02 September 14 | Time: 12.30-1.30pm (AEST Bris, Syd, Melb)
Click the title to register.

August 2014

News Release: Iced Tea Party™ Campaign the coolest yet

Throughout February and March, the Iced Tea Party™ campaign has generated more than $22,000 to support lymphoedema research and education – making this year’s campaign the most successful yet.

Click on the title above for more information.


August 2014

Access to treatment for breast cancer-related lymphoedema in Australia

Please click here to access the article on a study undertake by Robyn Sierla about Australian Breast Cancer Lymphoedema services in Australia published in the Australian Family Physician Dec 2013


August 2014

Lymphoedema Compression Garment Funding Information for Australia

Click on the title above to review the availability of Compression garment funding to the public within Australia.



August 2014

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SAVE THE DATE: Last weekend in May 2016 in Darwin for the Combined ALA and International Lymphoedema Framework Conference.

More information soon.

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