David Tuller
David Tuller
@david@trialbyerror.org

Senior Fellow in Public Health and Journalism, Center for Global Public Health, UC Berkeley. My academic position is largely funded by donations from patients. This account is an automatic WordPress-to-Fediverse feed; replies here will not be seen.

776 posts
83 followers
  • Time’s Health100 List Includes Leaders in Long Covid and ME/CFS

    Last week, Time magazine unveiled a list called the TIME100 Health—a selection of “leaders from across industries—scientists, doctors, advocates, educators, and policy-makers, among others—dedicated to creating tangible, credible change for a healthier population.” Time also wrote this: “Together, they are a reminder that many things are going right, and their work is enough to inspire…

  • A Conversation with the Co-Founders of The Sick Times

    Journalists Betsy Ladyzhets and Miles Griffis are the co-founders of The Sick Times, a non-profit that covers Long Covid and other chronic infection-related illnesses. They launched the site last November and have built up a solid following for their reporting, updates, and weekly newsletter. They recently received a $250,000 grant that will allow them to…

  • Interview with Co-Organizator of Next Week’s Unite To Fight Long Covid Conference

    Marco Wetzel, a digital sales expert, is one of five German Long Covid patients who banded together earlier this year with an ambitious plan to produce a major online conference called UniteToFight. Although they faced some initial skepticism, they quickly rounded up some high-profile names as speakers for the free event, including Pulitzer-Prize winning journalist…

  • Berkeley’s May Crowdfunding Campaign Begins…

    Berkeley’s latest crowdfunding campaign for Trial By Error begins today. It is hard for me to believe that I have been working on this project—debunking awful research into what was then called “chronic fatigue syndrome,” and related issues–for ten years. My efforts began in the summer of 2014, when I traveled to the UK to…

  • Australian GP Group Recommends “Incremental Physical Activity” for “CFS/ME” Patients

    What’s going on with Aussie members of the graded exercise therapy cult? (Oops!—I meant the Royal Australian College of General Practitioners, a trade and professional organization. Sorry!) In 2019, I wrote about the organization’s guidance for “CFS/ME.” This guidance, published in 2015, was part of the group’s Handbook of Non-Drug Interventions (HANDI). This month, HANDI…

  • Guardian Columnist George Monbiot Discusses His Scathing Rebuke of the Biopsychosocial Brigades–Text Version

    Last week, I spoke with George Monbiot, a British investigative reporter and political activist, who has been a columnist for The Guardian for almost 30 years. He and I have been in occasional communication in recent years over an issue of mutual interest—the scandalous mistreatment of patients suffering from the devastating illness (or cluster of illnesses) known as…

  • Guardian Columnist George Monbiot Discusses His Scathing Critique of the “Biopsychosocial” Approach to ME/CFS and Long Covid

    Earlier today I spoke with George Monbiot, a British investigative reporter and political activist, who has been a columnist for The Guardian for almost 30 years. He and I have been in occasional communication in recent years over an issue of mutual interest—the scandalous mistreatment of patients suffering from the devastating illness (or cluster of…

  • Senator Bernie Sanders’ $10 Billion Long Covid “Moonshot” Proposal

    On April 9th, Senator Bernie Sanders, the independent senator from Vermont who votes with the Democrats, unveiled an ambitious $10 billion “moonshot” proposal to fund research into Long Covid. The proposal has raised hopes among patients with the disease or cluster of diseases now being called ME/CFS—as well as concerns that those who came down…

  • An Interview with the Authors of the European ME Alliance Survey of 11,000+ Patients

    Earlier this month, the European Myalgic Encephalomyelitis Alliance (EMEA) released a 235-page report on a survey of ME/CFS patients in Europe titled “Same disease, different approaches and experiences.”  The authors are Arild Angelsen, a board member of the Norwegian ME Association and a professor at the School of Economics and Business at Norwegian University of…

  • REGAIN Team Responds to Criticism with Unconvincing Defenses of Methodological Missteps

    In recent weeks, I have been urging The BMJ to correct a flawed University of Warwick trial of an online mental and physical health rehab program for people with prolonged symptoms at least three months after hospitalization for Covid-19. The primary outcome was health-related quality of life, assessed with a measure called the PROPr score.…

  • A New Study from Exeter on “Brain Training” for Treatment of Post-Covid Cognitive Problems

    The University of Exeter is now recruiting for a study of “brain training” as a treatment for prolonged cognitive dysfunction after a bout of Covid-19. I found out about this via a post on X. The post highlighted a message that had been sent to an unidentified patient from their medical providers: “Are you experiencing…

  • In England, Conflicts Between Families and Hospitals Threaten the Lives of Young Women with ME

    ME patients and advocates in England have been alarmed by a series of ongoing cases in which the families of severely ill young women have struggled to convince hospitals to fit them with feeding tubes before they starve to death. I covered a similar situation last year in a piece about the life and death…