Myth vs Fact
Truth deserves the last word.
Myalgic encephalomyelitis (ME), also known as chronic fatigue syndrome (CFS), is a debilitating illness that affects millions of people worldwide. However, persistent myths and misunderstandings hinder its recognition and treatment. This year we are calling on you to help debunk six of the most common myths about ME and share the medical facts everyone should know.
With your support, we can change the narrative to get the facts right.
Challenge the myths, champion the facts.
ME knows no borders, and neither should our efforts to combat it. It is crucial that we work around the world to address this crisis.
COVID-19 continues to trigger a surge in the number of people affected by ME. Your voice is vital to ensuring this is addressed.
By fostering international cooperation, sharing research findings, and building recognition in every nation, we can pave the way for advancements in ME understanding and treatment.
Our goal is a world without ME.
Never underestimate the power of a share…
Challenge the myths, champion the facts. ME is a biological illness that disrupts the metabolism and impairs the brain, immune system and autonomic nervous system. #WorldMEDay #Fact
Find out more at worldmeday.org
Keep up to date by following us on social media!
Make a poster and stand up for the facts.
Add your photo and share the reality of ME.
Download your poster to share on social media, and you might be exhibited on our World ME Day 2025 gallery!
Read, share or print the ME Factsheet
Learn about what happens when you push through ME
Ivana
Brazil
“Please prevent thousands and thousands more people from developing ME.”
Mieko
Japan
“We deserve attention.“
Mlindeni
South Africa
“In my community, it’s taboo to be too sick.“
World ME Day News
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Country-by-Country Highlights for World ME Day 2025
Around the world, individuals, organisations and communities are coming together in to mark World ME Day 2025. Below is a breakdown of national events and campaigns happening by country, highlighting the wide range of efforts to raise awareness, push for better care, and demand action for people living with Myalgic Encephalomyelitis (ME). From media takeovers…
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Marking World ME Day: A Round-Up of Global Events and Tools
This World ME Day, on May 12th, communities around the globe are coming together to raise awareness, demand change, and support people living with Myalgic Encephalomyelitis (ME). From international conferences and grassroots activism to creative awareness-raising campaigns and vital educational tools, here’s a roundup of just some of what’s happening around the world this year.…
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World ME Day 2025: Six Myths and Facts Everyone Should Know About Myalgic Encephalomyelitis (ME)
Myalgic encephalomyelitis (ME), also known as chronic fatigue syndrome (CFS), is a debilitating illness that affects millions of people worldwide. However, persistent myths and misunderstandings hinder its recognition and treatment. Below, we debunk six of the most common myths about ME and share the medical facts everyone should know. Read on and share these graphics…
Check out our previous campaign videos and interviews
World ME Day is coordinated by the World ME Alliance and its members.
By focusing on a single day and collaborating across many organisations, we aim to maximise our collective power.
