Research Update from The Chronic Fatigue Syndrome Research Center (CFSRC) at Stanford University

Griffith University NCNED Makes Breakthrough in ME/CFS Research

pics of the research team outside and in the lab plus shots of logo lit up on the building for CFS Awareness week.711083, Professor Sonya Marshall Gradisnik, Professor Don Staines images for Louise Durack, OMC

Bio 21 Institute research – Inside Story report

Bio21_Melbourne University

Home

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 services and supports available right now.

About Emerge Australia

That’s what Emerge Australia is here to do: advocate for, educate about, and provide information on this debilitating condition.

Be involved

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