Barossa Lymphoedema Initiative

19/02/2026

Swollen feet and legs should never be dismissed as “just one of those things.”
Persistent, unexplained lower limb swelling can lead to infection, chronic wounds and long-term health complications if left untreated. With summer heat, travel, disrupted routines and dehydration all contributing to worsening symptoms, now is the time to talk about it.
Today, 19 February 2026, the ALA is proud to support national Beat the Swell Day, led by Wounds Australia - with ALA President, Kath Turner sitting on the panel of the flagship event, being hosted this evening.
Beat the Swell is an annual opportunity to raise awareness about:
• the causes of lower limb swelling
• the risks of leaving swelling untreated
• prevention and early detection
• effective, evidence-based treatment
The day brings together professional learning for clinicians and practical education for consumers, because awareness is the first step toward better outcomes.
Learn more via the home of Beat the Swell at woundaware.org.

17/02/2026

CONNECTIONS:
So important for us all. Lymphoedema Association Australia works on connecting you with like minded people through education and support. Join us to be part of this "connection".

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

13/02/2026

Who are we!
The Barossa Lymphoedema Initiative are Lymphoedema Therapists Gail Kirby and Kellie Thomas who are dedicated to providing specialised lymphoedema treatment and education for people living in the Barossa and surrounding communities.

Our mission is to ensure regional clients have access to high-quality, evidence-based care close to home. We offer personalised treatment, practical self-management education, and ongoing support to help individuals manage lymphoedema and improve their quality of life.

Compassionate, professional, and community-focused — we are committed to empowering our clients with knowledge, confidence, and care.

Send a message to learn more

12/02/2026

Follow us, as Gail & Kellie bring awareness to the Barossa & surrounds on Lymphoedema & everything Lymphatic over the March month.

Mark these dates on your calendar and watch this space. What are you thinking of doing to raise awareness of lymphoedema? Taking some LAA flyers and GP information brochure to your GP? Having a morning tea with friends? Writing to your MP?

https://www.lymphaustralia.org.au/

27/01/2026

Congratulations to our Patron, Professor Neil Piller on his Australia Day award, Member of the Order of Australia (AM) in the General Division for significant service to lymphology as a clinician and academic.
Neil has been our Patron since our launch in 2022. We couldn’t be happier for this well deserved award as he continues to work in the field of Lymphology.

https://www.lymphaustralia.org.au/

14/01/2026

Beat the Swell: a great campaign from Wounds Australia & a great joint initiative with Lymphoedema Association Australia who have registered Lymphatic nurses & Remedial therapists on their website for help.

In this interview with 9News aired on 14 January, Rockhampton-based lymphoedema expert Stacey Bradshaw and patient David Vickers explore lower limb swelling, and…

21/08/2025

Think you might have cellulitus or need information for your health professional about cellulitus?
The Australasian Lymphology Association has produced a handy resource for you and your GP.
Just a handy tip from one of our members: take a copy of this of you believe you have cellulitus when seeking medical attention.

https://www.lymphoedema.org.au/public/7/files/Position%20Statements/ALA%20Consensus%20Guideline%20Cellulitis-Rebrand%202019(1).pdf

13/08/2025

BAFC are an amazing group here in the Barossa Valley

We are trialing a Barossa support group for anyone affected by cancer, so please come along and join us. Talk to others who are sharing the same journey, with information, compassion, friendship and support. Casual and informal, we'll be getting together at The Clubhouse, 45 MacDonnell Street, Tanunda, on Monday 25th August at 11am. Everyone welcome for coffee and conversation.

04/08/2025

Though your generosity, Cancer Council’s Beat Cancer Project has invested $3.23million towards South Australian research projects in the past five years.

22/07/2025

13/07/2025

Hello SA,

We hope you are well and warm as winter sets in!

Below are our remaining events for 2025 and a Pdf is attached for anyone who is able to share our dates and we thank you in advance.

A shout out to anyone who is interested in joining our dedicated team of volunteers to help support the lymphoedema community of SA. We have our annual Planning Day on Saturday November 2nd to schedule our events for 2026 so if you think you might like to join us or would like more more information please send an email to secretary.lsgsa@gmail.com
The only requirement is a commitment to our cause and you will need to be an LAA member.

All the best from your SA Team - Ashlynne, Heather, Kellie, Kylie, Christina, Clare and Deb

Deb Hart
Lymphoedema Association Australia - SA Support Group
The LAA is the peak national organisation representing people across Australia living with or at risk of lymphoedema
LAA Website lymphaustralia.org.au
LAA Email admin@lymphaustralia.org.au
LAA Phone 1300 852 850

SA Support Group Contact secretary.lsgsa@gmail.com
Phone 0411 666 250

We acknowledge and respect the traditional custodians of the country whose ancestral lands we live, work, visit and travel upon.

12/06/2025

Peer support - locals that understand best

https://www.lymphaustralia.org.au/get-involved/support-groups-/