Lymphoedema Association Australia

Lymphoedema Association Australia Lymphoedema Association Australia is a passionate community of volunteers committed to ensuring no one walks their lymphoedema journey alone.

We want you to have support, information and resources to live your best life whilst managing lymphoedema. Welcome to Lymphoedema Association Australia (LAA). The Lymphoedema Association Australia is a national membership-based self-help organisation and offers support, information and education to anyone affected by lymphoedema. Founded in 2022 by people with lived experience of the condition and

health professionals, the LAA is a registered charity, with funds raised by membership fees, sponsorship, fundraising events, philanthropic trusts and tax-deductible donations. In forming the LAA, Lymphoedema Association of Queensland, Lymphoedema Support Group of NSW and Lymphoedema Association of Victoria, decided to close and merge their pages to become the Lymphoedema Association Australia Official page. PAGE RULES:
We do not allow defamatory, indecent, offensive, profane, or discriminatory postings or comments.
- Be kind and courteous: No offensive behaviour or abusive language will be tolerated. This should be a welcoming environment where everyone is treated with respect. Healthy debates are natural, but kindness is required.
- No hate speech or bullying: degrading comments about things such as race, religion, politics, culture, sexual orientation, gender or identity will not be tolerated. If you don’t have anything nice to say, then please do not comment, and rather scroll on!
- No promotions or spam: self-promotion, spam and irrelevant links are not allowed.
- No fraudulent, deceptive or misleading postings.
- No comments or postings infringing any laws including but not limited to copyright and intellectual property.
- Respect everyone’s privacy.
- Our community is a public place. Don’t post personal information that you would not be comfortable sharing with a stranger. We recommend that you don’t post any information that may identify you or anyone else, such as your address, email address or phone number.
- Page moderators will remove any post or comment contravening the page rules.
- Repeat offenders will be blocked.
- Any complaints are to be directed to [email protected]

This page is managed by the LAA Social Media Subcommittee. We will do our best to respond to you within 3 business days, however we may take longer during busy periods. We appreciate your patience. To review our vision, mission statement and goals visit: https://www.lymphaustralia.org.au/about-us/what-we-do

DISCLAIMER:
This page is administered by volunteers of the Lymphoedema Association Australia Social Media Subcommittee and as such we are unable to respond to medical or clinical questions or diagnose your condition. Information appearing on the LAA website and our page is for general information only. You should not use this information for diagnosis or treatment of your condition. Treatment should always be discussed with and practiced under the supervision of a qualified lymphoedema healthcare professional or your doctor. You assume full responsibility and risk of loss resulting from your downloading and/or use of files, information, other communications, content or other material (including but not limited to software or malware) accessed or obtained by means of the LAA social media sites. Mentioning of products or companies is not to be taken as an endorsement of that product/company by Lymphoedema Association Australia and its volunteers. Written or verbal communication from the Lymphoedema Association Australia constitutes information only. Results of any related actions remain the responsibility of the person(s) concerned. LAA expressly disclaims liability for actions taken or not taken based on any or all contents of its social media sites. Always consult with your health professional before changing your health activities. All links to other sites found linked from LAA social media sites are provided only as a service to users. Such linkage does not constitute LAA endorsement of those sites, or any information, product or service depicted on those sites. LAA are not responsible for the content of external sites. Please read the further disclaimer: https://www.lymphaustralia.org.au/_legal/disclaimer

PRIVACY:
The social media platforms utilised by LAA are not LAA websites or applications. We do not own, operate, or control these platforms and the LAA Privacy Policy does not apply. If you choose to provide information to these platforms through registration or other interaction, such actions are between you and the relevant platform. If you choose to register with any of these platforms, any information you provide is voluntarily contributed by you and is not maintained by the LAA. The LAA do not collect personally identifiable information such as your name, address or telephone number from its social media platforms. LAA will not contact you directly by phone, mail or email attempting to solicit information from you unless you request contact through private message or via email. For more information read: https://www.lymphaustralia.org.au/_legal/privacy

We are aware of some website issues and are currently working on it. In the meantime,  should you require assistance, pl...
18/06/2026

We are aware of some website issues and are currently working on it. In the meantime, should you require assistance, please don't hesitate to contact us by phone or the link below.

1300 852 850

https://www.lymphaustralia.org.au/contact-us/

What do you do to look after youself and show yourself some "self compassion"?A cup of coffee or tea?Stop and smell the ...
17/06/2026

What do you do to look after youself and show yourself some "self compassion"?
A cup of coffee or tea?
Stop and smell the roses?
Listen to the birds?
Some deep breathing exercises?
Take the dog...or just yourself... for a walk?
Exercise? Yoga? Tai Chi?
Meditate?
Whatever it is, be kind to yourself and acknowledge that while lymphoedema is a tough road you are doing the best you can.

These are just some of the wonderful positive ideaas and support that come from being in a support group.

Join LAA to access this and more resources before the end of this financial year and take advantage of all there is to offer.

https://www.lymphaustralia.org.au/membership/become-a-member/

Congratulations Helen Mackie on your King's Birthday Honour!!!'Helen MACKIEFor significant service to rehabilitation med...
16/06/2026

Congratulations Helen Mackie on your King's Birthday Honour!!!

'Helen MACKIE
For significant service to rehabilitation medicine, and to research and treatment of lymphoedema.'

Navigating compression and treatments for   can be a challenge. Our trade displays will give you a chance to look up clo...
16/06/2026

Navigating compression and treatments for can be a challenge. Our trade displays will give you a chance to look up close at some of the options available. Lymphoedema Association Australia is hosting a dedicated public information day in Melbourne, with researchers, therapists and of course trade displays. 📅 Saturday 20 June 2026 · William Angliss Conference Centre 🎟 Members $30 · Non-members $60

https://www.lymphaustralia.org.au/eventdetails/38302/live-well-with-lymphoedema-melbourne-public-information-day-vic to register

12/06/2026

Address

Brisbane, QLD

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