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.
06 October, 2022
NYC Women More Likely Than Men To Develop Long COVID: City Council Hearing
The New York City Council convened a hearing to recognize Long COVID’s disproportionate impact on women and gender minorities. Health experts testified that women are more likely than men to face debilitating long-term symptoms that push them out of the workforce, while patients and patient-advocates shared stories of dismissals from doctors and challenges with accessing financial support.
06 October, 2022
Biden Says The COVID Pandemic Is Over. He Could Have Fooled Me
An article by US ME/CFS sufferer Effie Seiberg.
06 October, 2022
New Ways To Treat Long Covid Might Be Here Sooner Than Thought
With mask mandates lifted and social gatherings occurring once again, people may be forgiven for thinking the acute threat of COVID-19 is over. But the shadow remains heavy for some, particularly for those suffering from so-called long COVID.
Due to COVID-19, it is difficult to plan face-to-face events. We are currently holding our Seminars and weekly social catch-ups on Zoom. Please check regularly for updates.
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.
