https://news.liverpool.ac.uk/2017/01/17/the-liverpool-view-post-ebola-syndrome-is-not-going-away/
Dr Janet Scott and Dr Calum Semple, from the University’s Institute of Translational Medicine, collaborate with the Ebola Survivor’s Clinic at 34th Regiment Military Hospital in Freetown, Sierra...
This is her response, for what it is worth:
I wonder what she offers to CFS patients: my guess given she is in the UK, it is probably CBT and GET. Does anyone know?
Could well be true, but when you do interviews for the media (as opposed to in private circles), your comments are justifiably scrutinised. And you have a particular onus on you to be accurate when you're not just presenting yourself as a patient but also as a medical expert.
Very frustrating he is still being adamant it's not ME or CFS. He was the same guy who wrote to BMJ blog post saying that the suggestion he had post viral fatigue syndrome was the worst suggestion he had been given.
http://www.meresearch.org.uk/may-competition-how-to-vote/
To facilitate sharing:
Edited to add:
By the way, for people on phones, it is at the bottom of the page, not on the right side.
"A logistic regression analysis of risk factors in ME/CFS pathogenesis" (Nov 2019).
Has data on lots of items in table 2 (see image for list) in an unadjusted form of simple numbers & %s in case you're interested in looking at data on your pet theories...
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