A national perspective for Myalgic Encephalomyelitis
ME/CFS Australia is the peak body for patient-led ME/CFS charities across Australia.
Advocacy | Education | Collaboration
ME/CFS Australia is the peak body for patient-led ME/CFS charities across Australia.
Advocacy | Education | Collaboration
Keep up to date with the latest news articles from around the world. Articles represent the views of their authors and not necessarily those of ME/CFS Australia. Some links lead to articles on third party websites.
Always seek advice from a registered health practitioner before changing your care plan.
Sleep In ME/CFS Shows Marked Night-To-Night Fluctuation Under Free-Living Conditions—Results From A Matched Case-Control Study
Research published in the Journal of Clinical Sleep Medicine.
Pituitary Gland Volume In Fibromyalgia Syndrome: A Case–Control Volumetric MRI Study
This study aimed to evaluate pituitary gland volume (PGV), pituitary gland height (PGH), and the frequency of ES in patients with Fibromyalgia (FM) using volumetric magnetic resonance imaging (MRI).
Trip Lee Opens Up About Chronic Illness, Worship Music, And The Lesson Every Mature Christian Learns
An interview with US Christian rapper, pastor, author, and ME/CFS sufferer Trip Lee.
World-leading, up-to-date, best-practice ME/CFS information collated by trusted leaders with lived experience.
ME/CFS Australia is a peak body for patient-led ME/CFS charities across Australia. Our focus is on advocacy with the federal government; research initiatives; national collaboration between organisations; and awareness campaigns.
We aim to improve access and inclusion for people with ME/CFS in health care, disability services, welfare, and other national services.
We do not offer member services to individuals as this is provided by local organisations. Find our local organisations.
You can also find peer support in the private Facebook group administered by volunteers from our member organisation, ME/CFS South Australia.
Incorporated in 1999, ME/CFS Australia Ltd is:
