Supporting
South Australians
with ME/CFS
by providing services, education and advocacy since 1987 for those with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.
Supporting
South Australians
with ME/CFS
by providing services, education and advocacy since 1987 for those with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.
Keep up to date with the latest news articles from around the world.
Articles represent the views of their authors and not ME/CFS SA. Always seek advice from a registered health practitioner before changing your care plan.
25 April, 2024
Are Monoclonal Antibodies The Future Of Long COVID Treatments?
The search for a cure to long COVID just got more promising.
25 April, 2024
World ME Day (May 12) Sheds Light On Global Health Crisis: Millions Affected By COVID Triggered Cases
The National Advisory on ME (ANZMES) is calling on Kiwis to come together for World ME Day as we battle a global health crisis. Already worldwide there are an estimated 25 million people with Myalgic Encephalomyelitis (ME) also known as Chronic Fatigue Syndrome (CFS).
25 April, 2024
Sanders’s Long COVID Funding Bill Misses Opportunity To Aid A Similar Chronic Condition
Sen. Bernie Sanders’ (I-Vt.) recent call for $10 billion in research grants over ten years for long COVID is a worthy initiative, yet we are deeply disappointed the senator is limiting his focus to long COVID. Millions of victims of infection-associated chronic conditions have been waiting decades for the federal government to fund research to improve diagnosis and develop therapies.
Find locally prepared information as well as resources and links from around the world.
We provide services that aim to meet the varying needs of our community.
We recognise that some people use the internet and some require hard copies; some members of our community can meet in person whilst others are housebound.