This week at The Sick Times, Elizabeth Pugh argues that labeling people with Long COVID as “patients” is stigmatizing and personally and politically harmful. “It strips personal agency,” she writes. “And frankly, it’s bad PR.” Read more: thesicktimes.org/2026/08/04/t...
The Sick Times
@thesicktimes.org
Award-winning nonprofit news site chronicling the #LongCOVID crisis. Founded by @BetsyLadyzhets.bsky.social & @MilesWGriffis.bsky.social Website: thesicktimes.org Newsletter: thesicktimes.org/newsletter Donate: the-sick-times.fundjournalism.org
Today @thesicktimes.org: Actor and playwright Elizabeth Pugh argues that Long COVID organizations should use person-first language, drawing on her own experience with HIV/AIDS activism in the 1990s. thesicktimes.org/2026/08/04/t...
There’s a long history of person-first language in advocacy. Here’s why we should use it for Long COVID. - The Sick Times
Labeling people with Long COVID as “patients” is stigmatizing and personally and politically harmful. It strips personal agency. And frankly, it’s bad PR.
thesicktimes.org
The U.S. is about a month into a summer COVID-19 wave, with levels rising across much of the country, especially in the West and South. This week's COVID-19 trends report: thesicktimes.org/2026/08/04/n...
From @thesicktimes.org: "Academically speaking, the neurological challenges are among the most concerning Long COVID effects. The cocktail of COVID19 and other pathogens that ran through my school every week, not just in the winter, kept students sicker and sicker." thesicktimes.org/2026/07/24/t...
The (sick) kids aren’t alright: Observations from a teacher with Long COVID - The Sick Times
We must help students by addressing Long COVID and advocating for clean air in schools.
thesicktimes.org
🧠 Small study: found persistent neuromuscular abnormalities in Long COVID 💊 Small trial: taking Paxlovid during acute COVID-19 may help reduce the risk of Long COVID ⚡️ Researchers announced a new, controversial trial to study the “Lightning Process” for Long COVID thesicktimes.org/2026/07/28/r...
Dysautonomia conference centers biomarkers and post-exertional malaise by Rachel Fairbank @thesicktimes.org thesicktimes.org/2026/07/28/d...
Dysautonomia conference centers biomarkers and post-exertional malaise - The Sick Times
The 14th annual Dysautonomia International conference outside Houston included presentations on the role of autoimmunity in dysautonomia and a biobank initiative for POTS research.
thesicktimes.org
The 14th annual Dysautonomia International conference outside Houston included presentations on the role of autoimmunity in dysautonomia and a biobank initiative for POTS research. thesicktimes.org/2026/07/28/d...
A thoughtful perspective from teacher Flynn Lovelace on what they've witnessed in classrooms since the pandemic. Children deserve the opportunity to learn, participate and thrive. We're grateful to see these experiences shared. 🧡 Worth a read. thesicktimes.org/2026/07/24/t... @thesicktimes.org
The (sick) kids aren’t alright: Observations from a teacher with Long COVID - The Sick Times
We must help students by addressing Long COVID and advocating for clean air in schools.
thesicktimes.org
The Sick Times: 'Dysautonomia conference centers biomarkers and post-exertional malaise' Written by Rachel Fairbank thesicktimes.org/2026/07/28/d...
Dysautonomia conference centers biomarkers and post-exertional malaise - The Sick Times
The 14th annual Dysautonomia International conference outside Houston included presentations on the role of autoimmunity in dysautonomia and a biobank initiative for POTS research.
thesicktimes.org
Today @thesicktimes.org: @sweetsciencewriter.bsky.social covers the recent Dysautonomia International conference! Featuring a new biobank initiative, presentations on autoimmunity, clinical trial results, discussions on the overlap of POTS and ME, and more. thesicktimes.org/2026/07/28/d...
Dysautonomia conference centers biomarkers and post-exertional malaise - The Sick Times
The 14th annual Dysautonomia International conference outside Houston included presentations on the role of autoimmunity in dysautonomia and a biobank initiative for POTS research.
thesicktimes.org
"The idea that exercise is the best medicine for all people with POTS still lingers. As Davenport noted, “We need to interrogate who has the fear here. We can’t be afraid of not exercising.” @sweetsciencewriter.bsky.social's write up on the DI conference for TST 🫀 thesicktimes.org/2026/07/28/d...
Dysautonomia conference centers biomarkers and post-exertional malaise - The Sick Times
The 14th annual Dysautonomia International conference outside Houston included presentations on the role of autoimmunity in dysautonomia and a biobank initiative for POTS research.
thesicktimes.org
A summer COVID-19 wave continues to pick up momentum in the U.S. While disease levels remain on the lower end compared to past summers, almost all major metrics are showing increases across the country. This week's COVID-19 trends: thesicktimes.org/2026/07/28/n...
Why is airborne disease transmission still controversial to doctors? In this week's episode of Still Here (@produced by @melaniemarich.bsky.social), co-hosts @mileswgriffis.bsky.social and @betsyladyzhets.bsky.social talk to Lola Germs about that and more. thesicktimes.org/2026/07/24/w...
"The quiet normalization of COVID-19 in our society has come at the great expense of school-age children and adolescents." thesicktimes.org/2026/07/24/t...
The Sick Times How to interpret clinical trial results for Long COVID thesicktimes.org/2026/07/21/h... Includes a section called "a crash course in statistics." Also links to this resource: Questions to ask when evaluating evidence from clinical trials. thesicktimes.org/2026/07/21/h...
How to interpret clinical trial results for Long COVID - The Sick Times
With no proven treatments or cures, many people with Long COVID are turning to off-label medications, supplements, and medical devices to treat their symptoms. There are numerous options — and some of...
thesicktimes.org
July is Disability Pride Month! Whether you’re a disabled journalist yourself or are able-bodied and wish to report on disability issues accurately, ethically, and respectfully, here are a few disability reporting tips based on our training last year with @thesicktimes.org & @newdisabledsouth.org.
Today @thesicktimes.org: Writer Flynn Lovelace shares his experience as a teacher with Long COVID, seeing signs of the disease among his students. "Since 2020, disease has held a constant, detrimental grip on classrooms across K–12 (and higher) education," he writes.
The (sick) kids aren’t alright: Observations from a teacher with Long COVID - The Sick Times
We must help students by addressing Long COVID and advocating for clean air in schools.
thesicktimes.org
Long COVID’s heterogenous nature means vast variations in symptoms and severity that may also make it more difficult to study and design good treatment trials. How do you separate strong studies from weak ones, and spot the bunk? Read more from @spichaksimon.bsky.social: bit.ly/4fxNWli
Thank you to everyone who became a Sick Times Supporter during our recent summer sustainability fundraiser. Thank you for refusing to stand by as other publications and people in power put the COVID-19 pandemic and Long COVID crisis in the past tense. ❤️
We keep seeing more signs that a summer COVID-19 wave is underway in the U.S. Still, as we’ve had a lower-than-average lull between waves this spring, recent levels are still very low compared to past summers. This week's COVID-19 trends: thesicktimes.org/2026/07/21/n...
"Like Mari, many disabled people rely on others to meet their most basic survival needs. When adequate support from governments and medical systems is not available, this level of dependency places disabled people at high risk of neglect, exploitation, and abuse." 1/3
Many disabled people rely on others to meet their most basic survival needs. When adequate support from governments and medical systems is not available, this level of dependency places disabled people at high risk of neglect, exploitation, and abuse. thesicktimes.org/2026/07/20/a...
Absolutely essential article from @crookedneighbor.bsky.social about the overlaps between anti-ICE organizing and Long COVID organizing at @thesicktimes.org: thesicktimes.org/2026/07/07/h...
How to protect your community from ICE when you have Long COVID - The Sick Times
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.
thesicktimes.org
Many disabled people rely on others to meet their most basic survival needs. When adequate support from governments and medical systems is not available, this level of dependency places disabled people at high risk of neglect, exploitation, and abuse. thesicktimes.org/2026/07/20/a...
I don’t think I’ve ever met Mari (a pseudonym), but her story is so deeply familiar to me and the things I’ve witnessed here in the States. Homelessness triggering Long Covid ME, triggering continued homelessness. Caregiver abuse that goes unrecognized as DV. Complete absence of social services.
Today @thesicktimes.org: Without help from government institutions, people like Mari, a young Black woman living in Canada with severe ME, are supported primarily by fellow people with severe symptoms. thesicktimes.org/2026/07/20/a...
Today @thesicktimes.org: Without help from government institutions, people like Mari, a young Black woman living in Canada with severe ME, are supported primarily by fellow people with severe symptoms. thesicktimes.org/2026/07/20/a...
Abandoned by our governments, people with severe ME and Long COVID are supported by severely ill peers - The Sick Times
Mari, a Black Canadian woman with severe myalgic encephalomyelitis (ME), is supported by fellow people with ME in the absence of institutional care.
thesicktimes.org
Many thanks for the shout out in the story about the op-ed the brave participants of the trial wrote for @thesicktimes.org last fall, calling for a better designed Vyvgart trial. thesicktimes.org/2025/10/10/v...
Vyvgart brought us back to life, but the Long COVID trial was canceled. We are calling on the NIH and HHS to study the drug. - The Sick Times
We are a group of 53 individuals with Long COVID from across the U.S. In 2023, we joined a Long COVID clinical trial for Vyvgart (efgartigimod), a drug approved by the Food and Drug Administration (FD...
thesicktimes.org
"When healthy people become ill, they expect to call a doctor, receive treatment, and recover. When people with myalgic encephalomyelitis (ME) become sicker, they often rely on other sick people for care, in the absence of systemic support." thesicktimes.org/2026/07/20/a...
Abandoned by our governments, people with severe ME and Long COVID are supported by severely ill peers - The Sick Times
Mari, a Black Canadian woman with severe myalgic encephalomyelitis (ME), is supported by fellow people with ME in the absence of institutional care.
thesicktimes.org
ALSO: big ups as always to @thesicktimes.org for covering long COVID so robustly and piquing my interest in Vyvgart for long COVID POTS.
👀 Study: COVID-19 can cause long-term eye disorders 🧠 New study: people with Long COVID may have dopamine system damage in their brains 💊 Clinical trial: some repurposed drugs were not effective in treating Long COVID fatigue thesicktimes.org/2026/07/14/r...