
Corporate interests have had more say in our behaviors toward both COVID-19 and the climate crisis than any evidence-based public health response.

Despite nearly 1.3 million deaths and counting, there is still not a national memorial for the pandemic. Our informal memorial in the middle of the Mojave Desert is one small way to remember those we’ve lost so far.

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.
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