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I wonder if Retraction Watch will do a piece on these news? They've done several on PACE.

Excellent! Thank you, Andy!

MD Ingrid Rekeland up now from Fluge/Mella's team, and I think later Øystein Fluge. Rekeland speaks in Norwegian. Edit to add Slides in English RituxME in 2. revision in prestigious journal

Yes there is. I linked to it to the first post in this thread, but it's always useful with repetitions. Will try to keep it in mind from now on :-) https://melivet.com/2018/08/25/petition-to-help-norwegian-me-patients/

Prof. Jonas Bergquist speaking (in Swedish). Seems to be the same lecture he gave at the Stanford-symposium.

This blog post has now been translated into English which is easier to read than a google translation. It is so important to bring the lobbying og connections among these people out into the public. Thanks again, Nina for all you do! About the Recovery network Norway - and what ME patients are...

Per Fink in New York Someone uninformed or stupid or maybe both decided to invite Danish physician Per Fink to present at a conference on so-called psychosomatic medicine being held this weekend at Columbia University

Could this mean that some quality control is actually happening now at Cochrane regarding ME?

The Norwegian ME Association is organising a CFS/ME conference for researchers together with The Norwegian Institute of Public Health and the National Competence Service for CFS/ME. This will take place 26th - 27th Nov. As part of this conference, they invite the public to an open seminar about...

Swedish Sten Helmfrid has debated ME and research (such as the PACE trial) for quite some time on twitter and in Swedish media. He and Henrik Vogt has an exchange on Nina's latest blog post now on twitter. As not all the tweets are in English, I've translated most of them Sten Helmfrid: Nina...

A Norwegian national service for all kinds of family, carers and next-of-kind has interviewed the parents of a child with ME. Their girl was only five years old when she got diagnosed with ME. Her parents talk about the disease and their meeting with health care personell. Once a doctor didn't...

The plot thickens.. In her recent blogpost the initiator of this petition, Nina Steinkopf, writes that MD Henrik Vogt (leader of the "patient" organisation Recovery Norge who supports undocumented, alternative treatments for ME and supports the Competence Service for CFS/ME and their...