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…

Continue ReadingWhat’s happening around the globe for World ME Day?

New York Times Cites Solve M.E Whitepaper, Quotes VP of Advocacy Emily Taylor

This week, New York Times writer Peter Coy’s piece, “Pushing ‘Long Covid’ Sufferers Too Hard Could Cause Them to Crash,” cited our recently released whitepaper, Long Covid’s impact on adult... This post appeared first on Solve ME/CFS Initiative. Read More

Continue ReadingNew York Times Cites Solve M.E Whitepaper, Quotes VP of Advocacy Emily Taylor

Elevating stories of the #MillionsMissing to HHS leadership

#MEAction is advancing ME/CFS advocacy efforts through our ongoing engagement with U.S. federal agencies, including at the Department of Health and Human Services (HHS). We continue to fight for our government to do more to meet the needs of people with ME, and to ensure that the evolving Long COVID…

Continue ReadingElevating stories of the #MillionsMissing to HHS leadership

#MEAction Presents: Not Going Quietly Screening & Panel

We have a very exciting opportunity to come together and watch the award-winning documentary Not Going Quietly. We also have an amazing live panel set up to discuss it with us immediately afterwards. Terri Wilder will be moderating and she shares her enthusiasm with us in this short video: We…

Continue Reading#MEAction Presents: Not Going Quietly Screening & Panel

Charli Arcouette, notre porte-parole sera panéliste à une conférence des IRCM pour l’encéphalomyélite myalgique

Notre porte-parole, Charli Arcouette, participera à un panel de discussion dans le cadre d'une conférence donnée par les Instituts de recherches cliniques de Montréal (IRCM) sur les maladies mal comprises. Elle sera aux côtés de la Dre Émilia Falcone, du Dr Amir Khadir et de Jérémie Meier-Sénéchal (AQML)... Our spokesperson,…

Continue ReadingCharli Arcouette, notre porte-parole sera panéliste à une conférence des IRCM pour l’encéphalomyélite myalgique

Ask Congress to TREAT & CARE for Post-Infection Diseases During Advocacy Month

Advocacy Month is an opportunity to share the policy solutions vital to address the growing number of individuals suffering from ME/CFS and Long Covid.  ME/CFS devastated the lives of an... This post appeared first on Solve ME/CFS Initiative Read More

Continue ReadingAsk Congress to TREAT & CARE for Post-Infection Diseases During Advocacy Month

WMEA campaign film: Tell us what the world can #LearnFromME?

On May 12th 2022, WAMES is joining with other groups around the world as the World ME Alliance to launch the first World ME Day, and we’re asking “what can the world #LearnFromME?” The world must listen to people with ME in order to #LearnFromME. Help us make a campaign…

Continue ReadingWMEA campaign film: Tell us what the world can #LearnFromME?