We can’t talk about Long COVID without talking about ME/CFS.
ME/CFS is Myalgic Encephalomyelitis (misnamed as Chronic Fatigue Syndrome) – and studies show it may affect 50% of people with Long COVID. For ME Awareness Month, we’ve been gathering resources on care strategies, treatment, and advocacy.
Many people with Long COVID and associated diseases like ME/CFS are newly disabled, while others have been living with disability or complex chronic illness for a long time. And as in all our movements, these struggles are connected. As we’re fighting for pandemic justice, care and safety, we are also fighting for disability justice, health equity, body autonomy, racial and gender justice, healthcare not warfare, an end to genocides, and so much more.
NEW! Check out our ME resource list on our new webpage: longcovidjustice.org/me, or share our social post on Instagram or Facebook.