Resource
Lymphoedema and repeated infections- what to do?
Posted on August 23, 2026
Royal Australian College of General Practitioners has a resource document (2024) covering What is Lymphoedema? that you may wish to discuss with your GP regarding suspect lymphoedema and what tests may be conducted to assess your swelling.
Australasian Lymphology Association (peak body for lymphoedema in Australia and New Zealand) has published a position statement (August 2026) on “Management of Cellulitis in Lymphoedema/Chronic Oedema” for doctors and health providers.
There is also an information flyer on “Understanding Celllulitis in Lymphoedema and Cjronic Swelling” for members of the public, patients and their family.
Call 08 9383 3838 or Book an appointment online with LK Lymphoedema Centre for professional support for an assessment and management of swelling. This may be following unresolved swelling after 3 months in head-neck cancer, post-op knee replacement, slow-to-heal leg ulcers, leaky legs or after repeated infections has resolved (also known as recurrent cellulitis). You may ask your doctor to complete a referral for you if your medical history is complex.
Help! What do I do with swelling (Lymphoedema) after my Prostate Cancer?
Posted on July 1, 2023
Physiotherapist, Dr Jo Milios & Sexologist/Nurse Practitioner, Melissa Hadley Barrett based in Perth, Western Australia host The Penis Project. It is a podcast that covers topics on men’s private parts. Podcast Episode 138 from The Penis Project, titled ” Meet Brian and Vanessa – Recovery, Injections, Lymphedema, and 2-3 rounds” shares some insights on their journey dealing with the challenge. I am so proud and thank the hosts and Brian for coming forth to share such intimate details so that others can learn from his experience.
There is hope for management of lymphoedema swelling impacting on sexual function following Prostate Cancer. Do not despair, you can continue to have a quality of life, just work with your lymphoedema therapist.
What is lymphoedema? FAQs on Lymphoedema and Cancer
Posted on March 1, 2021
March 2021 is Lymphoedema Awareness Month once again. There are books available via iTunes’ Apple Books covering Lymphoedema. There is one from Professor Peter Mortimer on Lets Talk Lymphoedema (2017). This time I would like to share my thoughts on a Book by Dr Teresa Lee ( a physiotherapist, NSW Australia).
Her E-book is available on Apple iBooks and Amazon.com.au and print copies available at navlymph.onlineweb.shop
Navigating Lymphoedema – A Guide for Cancer Survivors (2020 version)
Disclosure: I received a free digital copy of the book from the author. However, the comments are mine.
I would like to congratulate Teresa for taking on such a huge task of collating and writing up a much-needed resource tailored for cancer survivors with lymphoedema based in Australia, particularly for those with breast cancer. Teresa’s book is well-structured, logical, and comprehensive in coverage of the commonly asked topics. She covered each topic with the salient points in an unbiased concise easy-to-understand style. I particularly like the “Did you know” snippets that attempt to address points of debate or frequently asked questions.
Lymphoedema is not an easy condition to explain or write about and I feel this book is targeted towards people with a higher level of health literacy. Although there are pictures and illustrations throughout the book, I would have loved to see more to enhance the visual appeal. Interestingly, in a few instances, I feel that Teresa is sharing her thoughts one-on-one in detail with us as health professionals. Hence, this book may also be suitable for health professionals new to lymphoedema or who want to know more about the condition.
Overall, this is a value-for-money book that I would not hesitate to recommend to those clients who seek more in-depth information, education, and a sense of empowerment to navigate their lymphoedema journey. A labour of love, thank you Teresa for your effort.
Her E-book is available on Apple iBooks and Amazon.com.au and print copies available at navlymph.onlineweb.shop
Navigating Lymphoedema – A Guide for Cancer Survivors
Lymphedema: How common is it?
Posted on June 28, 2019
Lymphoedema, also spelt as Lymphedema has been identified as an under-recognised medical problem because not much is known as how widespread is the problem. Personally, like other researchers, I faced issues attempting to seek research funding for lymphoedema studies as prevalence data especially of the non-cancer origin was general
ly lacking. I am so glad that this issue is finally over! There has been a break through of an immense scale. (more…)
To operate or not to operate? Risks involved with lymph-node transplant
Posted on January 5, 2017
Head and Neck Cancer-related Lymphedema
Posted on May 20, 2013
How to detect maybe its Head and Neck cancer- related Lymphoedema? Click here
Breast Cancer Related Lymphedema
Posted on May 3, 2013
Decisions about arm exercise after breast cancer related lymphedema. Click here courtesy of another website
What is Lymphoedema?
Posted on April 2, 2013
Also spelt as ‘Lymphedema’ in USA. For a simplified explanation, courtesy of National Cancer Institute, please click here
Neck Self Drainage video
Posted on January 1, 2013
This is a simple neck self manual lymphatic drainage by Heather in USA. Click here to watch her youtube video demonstration. Happy Holidays.
American Lymphedema Framework Project
Posted on December 6, 2012
Met tireless Professor Jane Armer at the National Lymphedema Network conference, Dallas. Updates on the USA and American Lymphedema Framework, click here
