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https://www.crowdfunder.co.uk/tackling-the-mecfs-issue

Prevalence and incidence of myalgic encephalomyelitis/chronic fatigue syndrome in Europe—the Euro-epiME study from the European network EUROMENE: a protocol for a systematic review https://bmjopen.bmj.com/content/8/9/e020817

I think this is the best thing about the statement. Can PACE claim to have any patient support now?

It was mentioned in a Facebook post discussed here: https://www.s4me.info/threads/don-staines-and-griffith.5233/#post-94625

A reply to the article: https://www.bmj.com/content/362/bmj.k3621/rr

http://pubs.rsc.org/en/Content/ArticleLanding/2018/AN/C8AN01437J#!divAbstract

https://www.bbc.co.uk/news/health-45114842

https://www.bsms.ac.uk/about/contact-us/staff/dr-jessica-eccles.aspx As an MRC Clinical Research Training Fellow she recently completed her PhD in the relationship between joint hypermobility, autonomic dysfunction and psychiatric symptoms

Interesting article on iNews website. Looks like he tried a variety of things so I'm not sure any one thing can be given credit, he may have just improved over time anyway. https://inews.co.uk/news/health/marathon-runner-quit-work-me-cfs-diet-change/

Another cerebral blood flow study by the same authors discussed here: https://www.s4me.info/threads/task-related-cerebral-blood-flow-changes-of-patients-with-chronic-fatigue-syndrome.3155/#post-56205

https://patientworthy.com/2018/06/04/state-chronic-fatigue-syndrome-research-2018/ Comments are allowed. Perhaps people could thank the author and add to the information in the article.

A good article on Your Care Everywhere website. https://www.yourcareeverywhere.com/health-research/health-insights/pain-care-insights/stop-exercising-for-chronic-fatigue-syndrome-symptoms.html

I wonder if this evidence is coming from the NIH study in which Brian is a patient?

An email sent out from the Open Medicine Foundation by Ron Davis A Glimpse into My London Talk Dear John, I prepared this statement for Ashley Haugen to read yesterday at the Western Massachusetts Department of Public Health screening of Unrest. This is new information from the Severely ill...

I can honestly say I am the exact opposite of every single one of those characteristics

The ME Association are highlighting the call for videos for the Sky One series What's Up TV http://www.meassociation.org.uk/2018/05/whats-up-tv-sky-one/

54 MP's have now signed including my MP George Howarth (I only emailed him on Sunday so it's still worth trying) https://www.parliament.uk/edm/2017-19/1247

The Birmingham Mail is covering ME Awareness week with this story of a sufferer https://www.birminghammail.co.uk/news/health/illness-sucking-life-out-millions-14611319

The article is dated 1st May 2006. Does anyone know the outcome?

The Liverpool Echo is giving the documentary a mention https://www.liverpoolecho.co.uk/news/liverpool-news/bootle-mum-who-can-only-14622794 They originally covered her story on mother's day (along with the Daily Mirror) Mentioned in this thread here...