
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.

No ring-fenced research funding. No care pathway for the very severe. Hospitalized patients still at risk of malnutrition. What has the delivery plan really changed for people with myalgic encephalomyelitis in the United Kingdom?

Long COVID disrupts struggles for justice, as activists and organizers with the disease are forced to suspend or change their tactics, facing a community that largely ignores COVID precautions.

While the multi-billion dollar Long COVID Moonshot bill is currently stalled, advocates learned many important lessons that the community must carry into future efforts.

The demonstrations, organized by the group #LiegendDemo, took place in 42 cities across the country. Advocates demanded an end to “psychosomatic treatment of ME,” mandatory training for medical professionals, and large scale public health campaigns, and more. To mark International Myalgic Encephalomyelitis (ME) Awareness Day, advocates participated in marches and “lie in” protests in 42…

We spoke with the two organizations behind the viral moment where advocates interrupted speakers at the Long COVID EU Project event.

Our webinar answered common questions about following data for COVID-19 and other infectious diseases.

Long COVID, which has affected more than 400 million people around the world, is often underreported, particularly in low- and middle-income countries (LMICs).

With her #PodSaveJon campaign, she helped deliver one of the Long COVID movement’s best moments.

Long COVID Awareness Day is gaining official recognition around the world, driven by a growing network of people with Long COVID and their allies. In our season two premiere of Still Here, hosts Betsy Ladyzhets and Miles Griffis talk to Nicholas Rodelo of Clean Air Los Angeles about how he and his fellow organizers secured…
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