
Despite prior experience working in public health, I’ve faced challenges getting care for Long COVID and chronic seizures.

Essays documenting the toll that myalgic encephalomyelitis (ME) has taken on one family, from the new book, ‘What Is Myalgic Encephalomyelitis Like?’

Cancer has a sadly well-worn path. It showed me that I deserve dignity and support for Long COVID.

Essays focusing on Severe Myalgic Encephalomyelitis (ME), from a new book by an international group of writers documenting their ME experiences.

Labeling people with Long COVID as “patients” is stigmatizing and personally and politically harmful. It strips personal agency. And frankly, it’s bad PR.

We must help students by addressing Long COVID and advocating for clean air in schools.

Mari, a Black Canadian woman with severe myalgic encephalomyelitis (ME), is supported by fellow people with ME in the absence of institutional care.

From friends to medics, women are used to having their health issues dismissed, minimized, or blamed on their hormones.

People are taking on immigration enforcement from bed and the streets. We talked to two organizers for tips to participate in resistance while staying safe.

Before I started working at The Sick Times as your friendly neighborhood engagement editor, I let every medical professional I met bulldoze me.
advocacy arts CDC clinical trials commentary COVID-19 precautions disability essay government policy H5N1 healthcare HHS influenza international Long COVID in children masks and respirators ME ME/CFS medical education national COVID-19 trends NIH NIH RECOVER podcast public health research update science Trump administration updates and events vaccines wastewater surveillance