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.
20 April, 2021
How The Able-Bodied Can Do Better With Disabled Neighbors Like Me
An article by US ME/CFS sufferer Litsa Dremousis.
19 April, 2021
I Am 18 And Chronically Ill. Yes, I Am Just As Valid.
An article by Fibromyalgia sufferer Charlotte Stewart.
18 April, 2021
Living With Long COVID, 1 Year On
My experience with COVID-19 began on March 9, 2020. I’d generally been feeling under the weather, but I had a work event to go to. So, that morning, I got up, got dressed, and walked out of the door.
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.
