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“Hope to outlast the storm”: How severe ME impacts two brothers
Essays documenting the toll that myalgic encephalomyelitis (ME) has taken on one family, from the new book, ‘What Is Myalgic Encephalomyelitis Like?’ Read more…
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Policy & Advocacy
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Congress’s 2027 budget could include new funding for Long COVID and ME
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How to protect your community from ICE when you have Long COVID
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Wastewater testing is vital for public health. It needs sustained funding to continue beyond fall 2026.
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I worked in homeless services for years. It didn’t help me find accessible housing when I got Long COVID.
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The U.K.’s plan for ME has failed us. Members of parliament must step up.
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How is Minnesota addressing Long COVID?
Science
Covid-19
Health
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Breast cancer exposed the lack of care I receive for Long COVID
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VIPER aims to fast track Long COVID biomarkers. Here’s how it works.
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How do you spot Long COVID misinformation?
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Dysautonomia conference centers biomarkers and post-exertional malaise
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Experimental peptides are being advertised for Long COVID. But the evidence is trailing behind.
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Stop telling women their Long COVID is menopause
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“Hope to outlast the storm”: How severe ME impacts two brothers
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Breast cancer exposed the lack of care I receive for Long COVID
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“This exhaustion is cellular”: Excerpts from the new book ‘What Is Myalgic Encephalomyelitis Like?’
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There’s a long history of person-first language in advocacy. Here’s why we should use it for Long COVID.