Independent: Time for Unrest: Why patients with ME are demanding justice | 07 January 2018
A new film sheds light on a condition that is largely ignored. Nathalie Wright reports on the struggles patients face to be taken seriously by doctors.
A new film sheds light on a condition that is largely ignored. Nathalie Wright reports on the struggles patients face to be taken seriously by doctors.
Nature News Feature: A reboot for chronic fatigue syndrome research | 04 January 2018 Read More »
This is an excellent feature article that focuses on the developing research situation in America, but also includes items relevant to the situation here in the UK.
A recent scientific trial has led to acrimonious debates over chronic fatigue syndrome, aka ME, and boosted interest in a secretive therapy that some call a “cult” and others call a “miracle”.
The Hippocratic Post: Unrest – a new film about ME | 27 November 2017 Read More »
The following article appeared in The Hippocratic Post, and was written by Rebecca Wallersteiner, on 25th November, 2017. It features comment from Sarah Staples, and Dr Charles Shepherd, from the ME Association.
“Despite the headline negative finding, we believe that this trial will still provide useful insights and contribute to a better understanding of M.E., and we also have the results from the Cyclophosphamide clinical trial to look forward to. We are very pleased that this knowledgeable, and valued, research team will continue with their work, trying to find answers to the M.E. puzzle.”
Cara Tomas is a PhD student working with Professor Julia Newton at the Institute of Cellular Medicine, and her research was featured in the New Scientist last week.
UK ME/CFS Biobank: The importance of patient involvement | 06 November 2017 Read More »
Published in the Journal Fatigue: Biomedicine, Health & Behaviour,
BBC Breakfast with Jennifer Brea and Dr Charles Shepherd | 02 November 2017 Read More »
Last Saturday saw Jennifer Brea and Dr Charles Shepherd
By Dr Charles Shepherd, Hon Medical Adviser to the
We wrote to Sir Andrew Dillon last Friday, with a covering letter (below) and enclosed the final petition – supported by 13,593 people.
Tomorrow (24th October) will see a very special lunchtime
The SMILE trial was an attempt to determine the efficacy
By Russell Fleming, ME Association. ME Association trustees and
ME Association Petition: M.E. is not a functional disorder | 27 September 2017 Read More »
The suspected neurological conditions guideline specifically refers to M.E./CFS as a ‘functional’ disorder, which it defines as being ‘driven by emotion’ that, ‘may mimic physical disease’.
Note: This blog has been updated at 08.22 on
The ME Association has spoken out robustly and campaigned
Forward-ME submission to NICE suspected neurological conditions consultation. There is
Published in Behavioural Sciences, 11 August 2017. In November
Published in the Journal of Health Psychology, 29 August
Published in Clinical Physiology and Functional Imaging, 07 August