I've done the survey. But I suspect this has more to do with them combining PIP and ESA assessments rather than actually improving the assessment process for 'clients'.
https://www.s4me.info/threads/uk-disability-benefits-esa-and-pip-updates-news-and-articles-2021.19246/page-2#post-359835
sadly...
KCL
17 November 2021
Researchers confirm link between testing positive for COVID-19 and fatigue and sleep problems
https://www.kcl.ac.uk/news/researchers-confirm-link-between-testing-positive-for-covid-19-and-fatigue-and-sleep-problems
Full title: Association of SARS-CoV-2 Infection With Psychological Distress, Psychotropic Prescribing, Fatigue, and Sleep Problems Among UK Primary Care Patients
Kathryn M. Abel, MD, PhD1,2,3,4; Matthew J. Carr, PhD4,5,6; Darren M. Ashcroft, PhD4,5,6; Trudie Chalder, PhD7; Carolyn A...
The Andreasson lab
https://www.su.se/english/research/research-groups/the-andreasson-lab?open-collapse-boxes=research-group-members,research-group-projects
Fatigue cohort: A longitudinal study of persistent complicated fatigue...
Abstract
Patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) differ for triggers, mode of start, associated symptoms, evolution, and biochemical traits. Therefore, serious attempts are underway to partition them into subgroups useful for a personalized medicine approach to...
yes quite but it seems to have now taken on a life of its own.
also if you do a search on 'nhs post-exertional malaise' ironically the main nhs england website myalgic encephalomyelitis/chronic fatigue syndrome comes up and yet there is no mention of post-exertional malaise.
this website has been updated in 2019.
Posted on 09/05/2019
The science behind why M.E. does NOT make you “lazy”
https://www.nrshealthcare.co.uk/articles/news/the-science-behind-why-m-e-does-not-make-you-lazy
have reported the link from the library thread https://www.s4me.info/threads/the-pace-trial.22088/ be amended to
https://www.qmul.ac.uk/wolfson/research-/current-research-projects/projects/pace-trial.html
I know that; I was mixing it up with the similar research that Crawleys lot are doing
https://www.s4me.info/threads/pomme-study-paediatric-outcome-measure-me-2020-crawley-et-al.19524/#post-331486
ME on its own still hidden away here
https://www.england.nhs.uk/ourwork/clinical-policy/ltc/our-work-on-long-term-conditions/neurological/
should this not be ME/CFS now?
Haven't read this
Transformation Guide for Commissioners
The work has resulted in publication of a report to support...
Don't know if these have been posted somewhere
FOI2017-020: Spending on MRC-funded trials PACE and FINE
Request date: 22 May 2017
Response date: 20 June 2017
8 files
https://www.whatdotheyknow.com/request/the_pace_trial_white_et_al_2011#incoming-329168
NOT a recent FOI but from 2015 following the IOM report; many familiar names, thought it might be of interest here.
https://www.whatdotheyknow.com/request/357691/response/883778/attach/2/FOI%20EH73066%20Redacted%20documents%20for%20release.pdf
Dr. Maureen Hanson directs the National Institutes of Health (NIH) ME/CFS Collaborative Research Center at Cornell University, the Cornell Center for Enervating Neuroimmune Disease, where she and her colleagues investigate the biological mechanisms underlying ME/CFS (myalgic...
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