32 organizations call for future pandemic preparedness to address infection-associated chronic conditions

Future pandemic preparedness will fail millions without explicit recognition of and research into infection associate chronic conditions. On 20th September 2023, the United Nations General Assembly adopted a Political Declaration on Pandemic Prevention, Preparedness and Response. The commitments outlined in this declaration are vital for enhancing global readiness to tackle…

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Expanding Access: Guide to Involvement Now Available in German and Italian

We are delighted to announce that the World ME Alliance has expanded its new resource, "Involving people with ME and energy limiting conditions" to include German and Italian translations, alongside the original English and French versions. This comprehensive guide is designed to promote the involvement of individuals who have Myalgic…

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Global Advocacy Leaders Speak Out on Post-Exertional Malaise for World ME Day

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…

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World ME Day 2022 roundup

After an incredible World ME Day we wanted to share some of the amazing progress made across the globe. As individuals and organisations, our community stepped forward to fight for people with ME everywhere. We're going to do this by country, because there is just so much to cover! This…

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What’s happening around the globe for World ME Day?

In the run up to World ME Day on the 12th May we’re sharing more about what our member organisations are up to! Today we’re hearing from organisations in New Zealand, Italy, the USA, Northern Ireland and the wider UK. Keep on reading to see how the power of collaboration…

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CFS/ME Associazione Italiana joins the World ME Alliance

Our Alliance is growing, and we a thrilled to announce that the CFS/ME Associazione Italiana is joining our ranks. This small organisation works incredibly hard to ensure that people with ME in Italy have access to the information and resources they need to get the healthcare they deserve. The organisation…

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CFS/ME Associazione Italiana

Member The CFS/ME Associazione Italiana is a small organisation working to ensure people with ME in Italy have access to information about their disease from across the world.  The organisation focuses on raising awareness, translating information and resources into Italian, and providing people with ME with information about their rights…

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