NEWS

People with ME deserve accurate ME/CFS education from the Centers for Disease Control, not discredited recommendations for CBT and GET.

This year’s #MillionsMissing, our community created some amazing videos that we are privileged to highlight. This is just a small sampling of the amazing videos that were shared with us. It would be impossible to include them all, but we thank you all for sharing!

Thank you for illustrating our common thread so that our governments and institutions can respond to this health crisis.

Welcome to April’s #FacetsOfME where we will focus on loneliness and how this illness affects our need for connection and relationships.

Over the last many months, social media platforms like Twitter, Facebook, and YouTube have been flooded with disinformation about COVID-19. We wanted to make you aware of the problem, equip you with tools for how to recognize and respond to disinformation, and enlist your help keeping our community safe. According to numerous reports , much of this disinformation comes from organized campaigns by domestic groups or foreign governments. They rely on a mix of fake acco

We're thrilled to welcome Jaime Seltzer as our Director of Scientific and Medical Outreach.

The Time for Unrest event at the Scottish Parliament on 30 th January was an opportunity to raise awareness of Myalgic Encephalomyelitis...