“What I am suggesting is that, however people refer to M.E., however people experience it, chronic fatigue is not the same thing.”
Tag: Joanne Hunt
ME Awareness: Covid-19, Chronic Illness and Unacknowledged Loss by Joanne Hunt | 04 May 2020
“I suspect that the losses faced by many people with M.E. are in some ways uniquely different to almost every other patient group.”
Stigma and Marginalisation: Research opportunity for people with ME living in the UK | 17 February 2020
Jo Hunt from the University of Derby is looking to recruit people with M.E. for her research study.