When clinicians lack the knowledge they need, patients are denied the care they deserve. To close the gap, the World ME Alliance has created and curated a Medical Education Hub. Click the play button below to watch a short demonstration video.
The Medical Education Hub:
- contains trusted, evidence-based resources to equip healthcare professionals, inform researchers, educationalists and policymakers, and improve the experiences of people with ME/CFS and their families;
- aims to foster a future where care is grounded in science, and shaped by dignity and compassion;
- provides a range of resources that vary in terms of length and format (e.g. webinars, documents);
- includes resources in various languages, currently including:
- English
- Spanish
- German
- French
- Dutch
- Italian
- Brazilian Portuguese
- European Portuguese
- Hebrew
- organises resources into categories, currently including:
- Full Guidelines
- Continuing Professional Development
- Severe ME
- Quick reference summaries
- Medicines
Find out more at https://worldmealliance.org/medical-education-hub/
Share your story of why medical education matters (using the hashtag #EducateME), and ask healthcare professionals to read our one-page document explaining how the Medical Education Hub can help.
And follow the World ME Alliance on social media to working together to keep up with our work to achieve change for people with ME around the world.
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.
