Today on World Lymphoedema Day, landmarks everywhere are shining their lights blue to raise awareness about Lymphoedema. As part of Lymphoedema Awareness Week and Lymphoedema Awareness Month during March, we'd like to acknowledge all those who live with this incurable condition, as well as the organizations who help and support them, both here in Australia and abroad. They include:
Lymphoedema Association Australia
Mission: To ensure people living with lymphoedema get the information, treatment and support they need to live well, regardless of where they live. Get involved or donate here.
Australasian Lymphology Association
The Australasian Lymphology Association (ALA) is committed to promoting the development of lymphology in Australasia. The Association will strive to improve the management of those with, or at risk of developing lymphoedema and enhance communication between health professionals, educators, relevant authorities and government in regard to oedemas and lymphoedema. Find a practitioner here or discover more about ALA.
LKN Foundation
LKN Foundation provides quality information on lymphoedema self-care for people affected by Lymphatic Filariasis and Podoconiosis related lymphoedema. Become a sponsor or learn more here.
Whilst lymphoedema isn't curable, we can stop progression with a combination of the right treatment and self-care. Let's unite to broaden awareness and help get resources to those who need them!