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Dr David Tuller: Reporting on ME, ME/CFS, long Covid, and "Medically Unexplained Symptoms"

Countrygirl

Senior Member
Messages
5,488
Location
UK
https://crowdfund.berkeley.edu/project/37217

PLEASE SUPPORT DAVID'S EXCELLENT WORK ON OUR BEHALF

Trial by Error Spring 2023
Trial By Error: Reporting on ME, ME/CFS, long Covid, and "Medically Unexplained Symptoms"
As in previous years, April is crowdfunding month at the University of California, Berkeley, and I am once again seeking funds to continue my work on ME, ME/CFS, “medically unexplained symptoms,” and now long Covid. These tax-deductible donations to Berkeley will support my academic position as senior fellow in public health and journalism at the Center for Global Health from June through December of 2023. The Center uses the funds to cover my salary and health insurance.
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A short recap
Many or most of you reading this will likely be familiar with some of my work, but here's a short recap. I launched the "Trial By Error" series with a 15,000-word investigation of the disastrous PACE trial, published on Virology Blog in October, 2015. The PACE trial tested graded exercise therapy and cognitive behavior therapy as treatments for ME/CFS. By now, I have written hundreds of blog posts about that piece of crap and other aspects of these issues not only in the UK but in the US, the Netherlands, Norway, Finland and many other countries. As part of this project, I also write commentaries for academic journals and stories for major news organizations.
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Some more background
In October 2021, after a years-long struggle, the UK’s National Institute for Health and Care Excellence released its new ME/CFS guidelines. NICE found that the evidence for the psychotherapy and graded exercise approach was all of "very low" or merely "low" quallty--as patients have known all along and as I have relentlessly asserted and documented in my work. The new guidelines aren't perfect but nonetheless represent an enormous improvement and a welcome reversal of the discredited psycho-behavioral approach championed by the so-called “experts” in the field.
But the struggle continues. Publishing guidelines is one thing; implementing them effectively is another. Opponents have mounted fierce protests against the new guidelines continue to promote the same unproven therapies they always have. Now they are applying the same template to long Covid and post-viral illness in general. If successful, this effort will end up undermining the progress that has been in the ME field.
Because of long Covid's range of reported symptoms, many people with the illness have medical issues unrelated to ME and will not receive an ME diagnosis. But a great many will. So examining long Covid in the context of these scientific debates over the source and cause of the devastating symptoms is critical to sustain the momentum of change in the ME domain and affirming the advances in the ME field that have been made to date.

One Final Note

Berkeley takes a 5% share as the university's standard fee for gifts, plus 2.5% as a crowdfunding/credit card fee. Therefore, adding 7.5% to your donation will ensure that the full amount you intend is going toward the project itself. The donation is tax-deductible (for US taxpayers at least).
Thanks so much for your support. I really, really appreciate it, especially at this time of global trauma.
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Tom Kindlon

Senior Member
Messages
1,734
I’ve donated and shared on Twitter (two accounts), Mastodon, Instagram, Tumblr and Facebook account (personal profile and my ME page).

Have highlighted a bit in these places before including daily tweets, or retweets of others, on Twitter.
 

cheeseater

Senior Member
Messages
182
I used to think it was just the US medical establishment that was really messed up. Then I read about the PACE studies from NHS and it was a real eye opener about how messed up Great Britain was, too.