Myalgic Encephalomyelitis, also known as Chronic Fatigue Syndrome (ME/CFS) is a severe, complex, acquired illness. Symptoms can include issues with; brain function, the gut, the immune, endocrine and cardiac systems.
Diagnosis of ME/CFS is difficult and more research needs to be undertaken. The condition is not well understood in the general community or in clinical professions. In fact, it is widely misunderstood and finding appropriate treatment and management tools is often very difficult.
The condition can have an extreme impact on a person and can limit their capacity to lead an independent, healthy and fulfilling life. Good management can help with some of the effects of the condition particularly in more mild/moderate cases, but there is no doubt that this condition changes the lives of those affected.
It is vitally important to the well-being of people affected by ME/CFS that the condition be widely recognised. This will improve the availability and access to effective diagnosis, treatment and management. In the meantime there are some services and supports available through membership with Emerge Australia.
We provide education, information and community level advocacy about ME/CFS.
2019 Health and Wellbeing Survey
Talking about ME – please write to your MP
Write a letter to your local Federal Member of Parliament, and tell them what ME/CFS means to you, and how they can help.