https://www.zoffness.com/resources/ I was seeking some chronic pain online support group information and ran across this noted pain psychologist. Her resources for patients page did not inspire confidence. The opposite, in fact. To me, this is troubling, akin to the relegation of ME/CFS to the dumping grounds of CBT, MUS, FND, BPS, etc. Note: This is not an ad hominem attack. I do not know the psychologist, nor have I read any of her work, previous to today.
Well, what do you expect from a psychologist? It's the 'if you have a hammer, everything looks like a nail' syndrome.
There's just no end to it. I had a terrifically itchy rash once---considered by MDs to be about the worst---then the rash went away, but i still itched. The dermatologist told me i had "phantom itch" and nothing could be done about it. ETA: Correction from "pain" to "itch" due to a cognitive error.
She has some liason with medical students and departments at UCSF, at least. My quip is that it's only psychologists who take on pain patients unless it's interventional pain practices. And these pain psychologists really inflate their agenda/facts to a degree that blows my mind.