Talk (no booking required, public) no abstract yet
Date: 28 January 2020, 12:15 (Tuesday, 2nd week, Hilary 2020)
Venue: University Department of Psychiatry
Headington OX3 7JX
Organising department: Department of Psychiatry
https://talks.ox.ac.uk/talks/id/5a0edd5a-46e6-4f9a-8cca-f139852175f5/
https://www.psychiatryadvisor.com/home/depression-advisor/addressing-depression-in-myalgic-encephalomyelitis-chronic-fatigue-syndrome/
edit to add: Not a recommendation. I started the thread because someone linked the article on another thread.
https://www.sciencedirect.com/science/article/pii/S0889159119310773
From a press release by the university: https://www.vai.org/pregnancy-related-depression-lena-brundin/
Hello tryptophan my old friend.
I frankly find it doubtful that cognition, thoughts and beliefs, play more than a minor...
Journal of Adolescence
Volume 75, August 2019, Pages 123-129
https://www.sciencedirect.com/science/article/pii/S0140197119301289
again using this proxy CDF (chronic disabling fatigue).
Is this now a formal diagnosis?
Or are they maybe, finally, realising that CDF does not equate to ME or CFS...
Systemic low-grade inflammation and subsequent depressive symptoms: Is there a mediating role of physical activity?
https://www.researchgate.net/publication/333056434_Systemic_low-grade_inflammation_and_subsequent_depressive_symptoms_Is_there_a_mediating_role_of_physical_activity
I saw this article (which is mostly about antidepressants) on the Human Givens Institute and thought it worth sharing as it is written by a psychotherapist...
This left me perplexed. Is it complete quackery or a promising diagnostic method?
https://www.tandfonline.com/doi/abs/10.1080/15622975.2019.1599143?journalCode=iwbp20
I haven't looked at this, but it sounds interesting and relevant.
It is accepted by the CBT-GET promoters that there are biological changes in patients with ME. A key part of their argument has always been that psychotherapy can bring about or reverse biological changes.
Here is a study that...
Some interresting considerations about trials methodology (CoI, selectivity in publishing trials with positive results, gap between patients selected and real life patients, scales, what is used as a placebo...)
Rings a bell...
Does anyone know if there have been any studies following the long term outcomes of people who exhibit what I would term physical signs and symptoms (diarrhoea, tremors and shaking, irritable bowel, chills, aphasia, ataxia... etc - see places like webmd for lists) which have been widely ascribed...
Thought this might be of interest.
https://academic.oup.com/rheumatology/advance-article-abstract/doi/10.1093/rheumatology/kez027/5366191
Sci Hub, https://sci-hub.tw/https://academic.oup.com/rheumatology/advance-article-abstract/doi/10.1093/rheumatology/kez027/5366191
Open access at https://onlinelibrary.wiley.com/doi/full/10.1002/capr.12141
Posting this as it has been highlighted in the comments of Spoonseeker's latest blog that the concept expressed in this review is to be used to 'lower the bar' that NICE uses to assess treatments by, and therefore "to...
Not read the whole thing but potentially they could be looking at some undiagnosed PwME here.
Open access at http://www.psychiatryinvestigation.org/journal/view.php?doi=10.30773/pi.2018.10.22.3
As retweeted by AfME
some bits are good, but
"
Action for ME continue to say that having a well informed GP to assist with both depression and ME is important. Having appropriate and different treatments are vital, so that the mental health treatments don’t make the neurological side of ME...
https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD012488.pub2/full
(none on ME or CFS considered or included, 2 by Chalder rejected, one on Fibromyalgia included)
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