ME/CFS in the Media – TODAY Show

ME/CFS & the Australian election

Health Minister Greg Hunt announces $3million for research into ME/CFS

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What is ME/CFS?

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

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.

Impact

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.

Support

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.

About Emerge Australia

We provide education, information and community level advocacy about ME/CFS. You can sign up to our monthly newsletter, or have the fortnightly Media and Research Digest come straight to your inbox.

Be involved

If you would like to be involved in making a noise about ME/CFS, become a member or become a community activist now.

Petition to add ME/CFS to List B of the National Disability Insurance Scheme

Sign the petition to demand better access to the NDIS for people with ME/CFS!

 

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Emerge Australia News

Mar 10

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