
In the News
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.
09 March, 2025
I'm A Long COVID Researcher—And I Have Long COVID
An interview with US long-COVID researcher and sufferer Alison Cohen, Ph.D., MPH.
09 March, 2025
Long Covid Warning: 'Silent Organ Damage Is A Real Problem'
Public health experts are urging the government to protect people from Long Covid, which they say could have already affected a quarter of a million New Zealanders.
08 March, 2025
Long Covid Update – A Threat That Continues To Demand A Strong Response
Long Covid (LC) remains a risk following any Covid-19 infection or reinfection. It includes a syndrome of long-term symptoms, a substantially increased risk of sudden death, and silent cell and organ damage that may predispose to later illness. Consequently, it produces a large burden of illness for our communities, healthcare system, and economy. Covid-19 vaccination reduces the risk of LC following Omicron infection, but there is still around a 10% risk of LC among vaccinated individuals.
08 March, 2025
Prospective Cohort Study Of Fatigue Before And After SARS-CoV-2 Infection In The Netherlands
Research published in Nature Communications.
07 March, 2025
Triathlon Prodigy Reveals How Life-Changing Illness M.E. Destroyed His Promising Career
Ireland's James Walton had the world at his feet prior to his diagnosis.
07 March, 2025
5 Myths About Chronic Fatigue Syndrome, Debunked
It’s time to get real about this commonly misunderstood condition.
06 March, 2025
Long COVID Journalists Share How They Founded The Sick Times
Frustrated with how the pandemic, COVID-19 information, and, especially, people living with long COVID have been left behind by mainstream media coverage, journalists Betsy Ladyzhets and Miles Griffis founded The Sick Times in 2023. The publication covers all aspects of COVID-19 and long COVID, including policy, research, lifestyle, and those affected by both conditions and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).
06 March, 2025
Kirklees And Calderdale Charity Tells The Government To Wake Up And See The Bigger Picture
A support group for people with ME in Calderdale and Kirklees have been reaching out to local MPs to demand that a long awaited government proposal, which promised to finally deliver a strategic plan, is actually given some funding to move forward.
05 March, 2025
Cerebrospinal Fluid Metabolomics, Lipidomics And Serine Pathway Dysfunction In Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
Research published in Scientific Reports.
05 March, 2025
Katie Boulter’s Net Worth, Alex De Minaur Relationship And Struggle With Chronic Fatigue
Professional tennis player Katie Boulter was diagnosed with chronic fatigue syndrome (CFS) back in 2016, a condition that has affected the careers of many athletes.