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https://www.researchnet-recherchenet.ca/rnr16/viewOpportunityDetails.do?browseArc=true&fodAgency=CIHR&org=CIHR&progCd=10866&view=browseArchive&language=E

News update, link to program on the page https://www.newswire.ca/news-releases/experts-gather-in-montreal-to-develop-international-research-agenda-on-myalgic-encephalomyelitischronic-fatigue-syndrome-680811321.html

I wouldn't mind volunteering for this as long as they allowed me to film them filming me and when it was over we could sit down and watch my film and they could describe their thoughts and feelings and emotions on having wasted their careers.

I think it's a case of creating demand for their own services at the cost of the taxpayer (and the people sectioned). There simply aren't enough people prepared to hand over their own money to sustain such a growing bunch of fraudsters.

Cardigans?

I honestly think that CBT is just a service offered by psychiatrists to doctors allowing them to get rid of patients who they can't help but who keep coming back to them asking for help.

Or what should we do when the brain-washing wears off.

This page is listed as being updated April 2018. Not sure what has been changed but there are some good points in it. https://www.health.ny.gov/diseases/conditions/me-cfs/

Says it all really

https://www.liverpoolecho.co.uk/news/liverpool-news/devastating-leaves-teen-girl-unable-14534145

The Faculty Lounge is covering the appeal. http://www.thefacultylounge.org/2018/week14/index.html

So Action for ME has no record of who was representing it during the biggest most expensive study into ME? Are charities not obliged to keep records?

Google Translate: 30 March 2018: UWV draws conclusions from the Health Council on ME Insurance physicians at the UWV must take into account the advice of the Health Council on ME / CFS: "Insofar as insurance physicians consider CGT and GET as an effective therapy and a client is more or less...

From a Cort blog https://www.healthrising.org/blog/2017/09/30/three-nih-funded-mecfs-research-centers-controversy/

ME Action is now highlighting these vacancies https://www.meaction.net/2018/03/26/cfs-advisory-committee-seeks-voting-members/

My tinnitus only affects my right ear and is the only predictor of a flare up in my ME symptoms. When I go to bed and I can hear the buzzing in my right ear I know I have overdone things that day and will be ill when I wake up in the morning. The buzzing will remain for a few days but will...

Van der Meer has responded to the report https://www.ntvg.nl/artikelen/gr-rapport-over-chronische-vermoeidheidssyndroom/abstract

Anyone interested in applying? DEPARTMENT OF HEALTH AND HUMAN SERVICES Solicitation for Applications from Individuals Interested in Being Appointed to the Chronic Fatigue Syndrome Advisory Committee https://s3.amazonaws.com/public-inspection.federalregister.gov/2018-05833.pdf

https://uk.linkedin.com/jobs/view/research-associate-fitnet-nhs-trial-at-university-of-bristol-625224811

Let's hope the final version is close to the draft