ACT ME/CFS Society, Inc
Provide support and information for people affected by ME, CFs & FM in the Canberra region, monthly support group meetings, a self help course and Telephone Information and Support Service (TISS).
Change for ME Australia
Change for ME advocates for: Greater understanding of the condition in the medical community and general public, increased support and medical access for ME & CFS sufferers to help address the poor quality of life & elevated risk of suicide.
Emerge Australia is a not-for-profit charitable organisation dedicated to providing information, support and advocacy for the ME/CFS community in Victoria, Tasmania and the Northern Territory.
ME/CFS Australia is an affiliation of autonomous state ME/CFS organisations. It operates at the national level, approaching ME/CFS issues from an Australia-wide perspective.
Alison Hunter Memorial Foundation
The Foundation is an enduring memorial to Alison Hunter and all those whose lives have been devastated by ME/CFS. The Foundation works in cooperation with all researchers, institutions and ME/CFS societies to advance scientific knowledge and medical care.
Australian Pain Management Association
APMA is a health promotion charity providing advocacy, information and practical support for people living with persistent (chronic) pain and their families.
Justice Connect works to provide effective means for people and organisations in need to access justice. They deliver access to justice through pro bono legal services to people experiencing disadvantage and the community organisations that support them i
Lyme Disease Association of Australia
An association comprised of volunteers committed to making changes to how Lyme disease patients are treated – both medically and personally. This is achieved through undertaking activities in four key areas of information, support, education and awarenes
Free online magazine published by ME Research UK approx. twice a year with research news from around the world & other ME/CFS issues.
ME/CFS and Fibromyalgia Information Exchange Forum. The world’s largest ME/CFS email news-list service.
Advice to help people manage ME and hopefully even look forward to getting at least partly better…
Cort Johnson’s blog. Health Rising is dedicated to providing timely, accurate information to people with Chronic Fatigue Syndrome (ME/CFS) and Fibromyalgia.
Phoenix Rising provides people with chronic fatigue syndrome (ME/CFS) information to support their health and wellness and online programs to enhance their health and well-being.
Action for M.E. (UK)
Action for M.E.’s mission is empowering people with M.E. to fulfil their potential and secure the care and support they need, while working towards a greater understanding of the illness and ultimately a cure.
“The bad news is we don’t know what causes it or how to treat it successfully.
But the good news is that there are now over 4,000 published studies that show underlying biological
abnormalities in patients with this illness. It’s not an illness that people can just imagine that they have,
and it’s not a psychological illness. In my view, that debate,
which has raged for 20 years, should now be over.” – Dr. Anthony Komaroff,
CFS clinician and researcher, Harvard Medical School (2006 Press Conference)