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.
'I Was A Bedbound ME Sufferer, But I Can Offer Hope'
A man from Leatherhead in the UK who spent a decade bedbound with chronic fatigue syndrome said he is "learning how to interact with the world again".
Fibromyalgia Common In Women With Chronic Pelvic Pain
Women with chronic pelvic pain are 3 times more likely to have fibromyalgia compared with women without chronic pelvic pain, according to study results published in Advances in Rheumatology.
Trial By Error: Springer Nature Removes Description Of “Fatigue” Patients As “Combative” And “Reproachful”–UPDATED
An article by US journalist and ME/CFS advocate David Tuller, DrPH.
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:
