Source: Journal of Health Psychology
Preprint
Date: March 21, 2019
URL: https://journals.sagepub.com/doi/full/10.1177/1359105319834678
Acceptance and identity change: An interpretative phenomenological analysis of carers' experiences in myalgic encephalopathy/chronic fatigue syndrome...
My interpretation: "If we tell people how they should have answered then they answer more correctly the second time around", or have I misunderstood something here?
Open access at https://www.tandfonline.com/doi/full/10.1080/23279095.2018.1519509
"In the following discourse I shall endeavour to shed light on how, and perhaps why, a serious disease has not been taken seriously for nearly half a century. The disease is Myalgic Encephalomyelitis. Many people think it is the same thing as Chronic Fatigue Syndrome but I shall also explain why...
In Chicago Evening Post:
"TORONTO, ON, CANADA – 06-05-2018 (Press Release Jet) — Like many people, Faith always assumed if she fell ill she would be covered by her group benefits insurance company if there ever came a time when she wasn’t able to work. Unfortunately for this 40 year old from...
I thought I might have seen this posted somewhere but can't find it.
It says 2018 but from the link it might be from 2016.:
"
Alison Millington
Mar. 22, 2018
"
Living with CFS feels like being tired all the time — but it's so much more than being tired.
The illness is thought to affect at...
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