We are thrilled to announce the newest member of the World ME Alliance: Neúnavní. This Czech charity is dedicated to supporting individuals living with Myalgic Encephalomyelitis (ME) in the Czech Republic. Neunavní has been at the forefront of raising awareness, providing resources, and advocating for better care and understanding of…
Myalgic Encephalomyelitis (ME) is a debilitating and complex condition that affects millions of people across the globe. On May 12th, World ME Day is observed to raise awareness of this chronic illness, and to advocate for the millions of people who live with it. The disease where pushing harder can…
World ME Day takes place on May 12th to raise awareness of myalgic encephalomyelitis (ME), a debilitating and often misunderstood illness. This year, organizations from around the world have come together to host events and activities to support those living with ME and promote understanding and action on a global…
Final call-to-action for World ME Day 2023. Follow Holly's example and tell the world what happens when pushing harder makes you sicker for World ME Day. https://youtu.be/EWrA7_zvf8U ME, or Myalgic Encephalomyelitis, is a debilitating disease that affects millions of people worldwide. One of the most debilitating symptoms of ME is…
Share the reality of how pushing harder can make you sicker. The WOrld ME Alliance and it's members are calling on all people with ME and carers to demonstrate the reality of living with ME for World ME Day 2023. Let's make post-exertional malaise visible. When it comes to ME,…
We are excited to announce the launch of our new factsheet on myalgic encephalomyelitis (ME), with a particular focus on post-exertional malaise (PEM). Available in four languages, we hope this resource will help build a basic understanding of ME across borders. Myalgic encephalomyelitis (ME), also known as chronic fatigue syndrome…
To mark World Health Day, and with just over one month to go until World ME Day, we are launching our next resource! Are you interested in helping to raise awareness for myalgic encephalomyelitis (ME), a chronic and disabling disease that affects millions of people worldwide? If so, you're invited…
As we approach World ME Day on May 12th, the World ME Alliance is excited to announce the launch of six new graphics that explore different aspects of post-exertional malaise (PEM). These graphics are available for download and use by anyone, with the aim of raising awareness about the impact…
We are thrilled to announce that Millions Missing Mexico, a voluntary organisation dedicated to raising awareness about Myalgic Encephalomyelitis (ME) and supporting patients, has joined the World ME Alliance as its 22nd member and the first member from Latin America. Millions Missing Mexico was founded in 2018 by a group…
Member Millions Missing Mexico is a voluntary organisation dedicated to raising awareness about Myalgic Encephalomyelitis (ME) and supporting people with the disease in Mexico. The organisation was founded in 2018 by a group of people with ME and their caregivers who were frustrated by the lack of knowledge and resources…