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Gather a lot more data about the practises, attitudes, knowledge and patient outcomes in standard practise (in a way that doesn't allow those physicians to report in a deceptive way). I'm proposing a lot more study of physicians themselves. Physicians should be experimented upon, not just patients.

from: racpcongress com.au/speaker/ms-megan-mcewen/ www racp edu au/docs/default-source/events/congress-2019-presentations/racp-tues-7-masterclass.pdf?sfvrsn=619a181a_2 www meganmcewen co nz https://web.archive.org/web/20190130090302/https://www.meganmcewen.co.nz/what-is-cfs...

Here is the "latest thought from Europe": https://www.sciencedirect.com/science/article/pii/S2213158219301482 The above review shows a striking lack of evidence of markers in the brain that are constant across functional disorders. I also think there is clear bias in the brain regions he has...

He uses those in the same way as SW: It's others describing such patients as those things, honest! I'm the one with the empathy for patients and telling patients their illness is real!

https://www.nzherald.co.nz/nz/news/article.cfm?c_id=1&objectid=12136294 https://www.nzherald.co.nz/index.cfm?objectid=12173126 "Managing Difficult Encounters Chris Kenedi M.D." http://www.gpcme.co.nz/pdf/2016 North/Thur_Room7_0830 Difficult pt and the brainGP CME 2016.pdf

My sympathy disappears when I discovered that most GPs don't bother regularly reading any peer reviewed research at all. I have asked doctors in many different social contexts and they all give the same answer - only doctors who do research, subsequently read research regularly. These GPs...

Yes, but not enough on its own. If she then reported that she had to spend the rest of the week in bed, it wouldn't exactly be considered a success.

War, violence, poverty, illness. None of it is a problem if we choose not to care. ;)

It's not a waste of time, it does not detract from the other problems unless we let it distract us.

One topic that seems to be doing the rounds is the idea that because the symptoms are now potentially explained by CCI that people with this illness never had "real ME". I think this is a distortion of what most people were saying and it is damaging to perpetuate these accusations. Those...

June 13th Editorial Biopolitics, psychosomatics, participating bodies - Monica Greco https://mh.bmj.com/content/early/2019/06/13/medhum-2019-011717 This is part of the overall project: www dot crassh.cam.ac.uk/events/26189 Still no sign of Sharpe...

The study is notable for making hundreds of statistical comparisons without using any sort of corrected alpha... https://en.wikipedia.org/wiki/Multiple_comparisons_problem They acknowledge it, but didn't bother to fix the problem... Amateur hour anyone?

Perhaps patient response inspired some extra peer review?

For balance (balancing out all the years of all-male panels), he should resign and adopt a 100% women panel policy in the NIH for a few years. ;)

The goal is to build research capacity - if they claim there is not enough applications to provide as much funding as the disease burden demands, they have to ask themselves why and address those concerns directly.