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.
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Suzanne O’Sullivan’s “Psychosomatic” Mis-Diagnoses
Neurologist Suzanne O’Sullivan has been conducting a media blitz for her new book, “The Age of Diagnosis: How Our Obsession with Medical Labels Is Making Us Sicker.” The Guardian ran a lengthy excerpt in early March. O’Sullivan appeared on the popular podcast Freakonomics. Multiple publications have published profiles of her, with credulous assessments of her…
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Some Things I’ve Read Recently…
Lisa McCorkell leaves Patient-Led Research Collaborative after five years… Way back in 2020, when it became clear that some people were experiencing prolonged symptoms after an acute bout of COVID-19, Lisa McCorkell helped found the Patient-Led Research Collaborative (PLRC). The organization grew out of an online health-related support group, which published the first survey on…
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Lancet Letter Exchange on Claimed Success of “Persistent Physical Symptoms” Trial Despite Clinically Insignificant Findings
Last year, The Lancet published a paper from Christopher Burton and colleagues called “Effectiveness of a symptom-clinic intervention delivered by general practitioners with an extended role for people with multiple and persistent physical symptoms in England: the Multiple Symptoms Study 3 pragmatic, multicentre, parallel-group, individually randomised controlled trial.” Per the norm for research on psycho-behavioral…
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New Study Documents Iatrogenic Harm from Perceived Psychosomatic and Psychiatric Misdiagnoses of Rheumatic Diseases
In 2020, I wrote a post about a paper, published by the journal Rheumatology Advances in Practice, called “Medically explained symptoms: A mixed methods study of diagnostic, symptom and support experiences of patients with lupus and related systemic autoimmune diseases.” The corresponding author was Melanie Sloan, a researcher in the Department of Public Health and…
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BMJ’s Strange Response to Our Letter of Concern Regarding “Living Systematic Review” of Long Covid Interventions
In December, I sent a letter, co-signed by 18 colleagues, to The BMJ‘s editor in chief, Dr Kamran Abbasi. The letter requested a correction to a problematic study called “Interventions for the management of long covid (post-covid condition): living systematic review.” According to this review, there is “moderate certainty evidence” that a physical and mental…
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A Reprise of a 2018 Post on My Visits with Alem Matthees
In 2018, I spent six weeks in Australia, visiting multiple cities on a kind of ME/CFS tour around the country. Near the end, I spent five days in Perth. The local patient and advocacy organization arranged for me to give a talk, do some lobbying with local government, and so on. But my main motivation…
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Our Presentation at the University of New South Wales
On Tuesday, I gave a presentation at the Kirby Institute, a renowned research center at the University of New South Wales in Sydney, along with my friend and colleague Dr David Joffe, a respiratory medicine specialist. David spoke about the pathophysiology of Long Covid as well as the enormous economic burden of the disease. I spoke about…
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My 2018 Post on Andrew Lloyd’s Memory Lapses, Revisited
Yesterday, in Sydney, I gave a presentation at the Kirby Institute, a renowned research center at the University of New South Wales, along with my friend and colleague Dr David Joffe, a respiratory medicine specialist. David spoke about the pathophysiology of Long Covid as well as the enormous economic burden of the disease. I spoke…
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A Bogus Request for Corrections to Recent Post on a Long Covid Exercse Study
Zachary Grin is a physical therapist in New York City who specializes in functional neurological disorder. Over the years, we had what I considered a good-natured, generally respectful exchange of views. As a gay man, I felt empathy for him—he posted about having difficulties with his parents after he came out. But I blocked him…
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Australian Survey Seeks Input for New ME/CFS Guidelines
Australia’s National Medical Health and Research Council (NMHRC) recently released what it calls a “scoping survey” as a first step in developing new clinical practice guidelines for ME/CFS. The survey was posted online on February 21st; the deadline for responding is April 27th. The plan calls for the new guidelines to be published in three…
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New Hyped-Up Lightning Process Study from New Zealand
In January, the Journal of Family Medicine and Primary Care published a paper from New Zealand called “An audit of 12 cases of long COVID following the lightning process intervention examining benefits and harms.” It reads like a Lightning Process marketing effort cosplaying as an academic study. As a reminder, the LP is a mish-mash…
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Some Things I’ve Read Recently…
With so many people impacted by Long Covid and ME/CFS, it is impossible to keep up with all the non-academic articles, posts, and commentaries out there. The gusher of material is really overwhelming. Given that, sometimes it seems worthwhile to highlight a few things worth reading. (Note: Recommending something as worth reading should not be…