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 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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Across the globe for World ME Day 2024
We are reporting on the advocacy, actions, campaigns and events of our member organizations and others across the globe for World ME Day 2024. Brilliant initiatives were held to make a difference on a local and global scale. Demonstrations, lobbying, art and education events were organized across six continents! Learn more about the incredible global…
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“Everyday I am walking the tiniest tightrope of forward progress” – Cynthia, USA
Name: Cynthia AdinigPronouns: she/herAge: 38Home: Alexandria, VA, USASick for: 4 years In March 2020 my family and I got a Covid infection so mild we were denied access to a Covid test. But on Mothers Day, May 10th 2020, my life changed forever when I had the first incident that sent me to the Emergency…
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Speaker Announcements for Bridging Borders livestream
On May 10th we’ll joining with advocates across the world to showcase the committed work of non-profit organisations, all building a #GlobalVoiceForME. Find out who is speaking and the range of topics they are covering! Speakers Mlindeni Gabela and Sam Pearce MELCuSA South Africa Reporting on the world’s first SICK Pride event Giada Da Ros…
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.
