I just clicked on the #cochraneforall hashtag and saw some very good tweets by PWME who were doing us proud. Thank you! :balloons:
Can you break your post up a bit please, @NelliePledge? A lot of us struggle with big blocks of text.
Yes, in Solve's tweet the weblink starts www.Solvecfs.org but it immediately takes you to this other thing. I agree!
This paper: The biological challenge of myalgic encephalomyelitis/chronic fatigue syndrome: a solvable problem by @Jonathan Edwards and several...
Bump! Starts in a few minutes.
I got to it direct from the link in Solve's tweet here: [MEDIA] Would you rather delete the thread if you think there's a problem?
This interview was published on Oct 11, 2017. I haven't seen it posted elsewhere. Haven't read it yet but it has a contents list! Introduction...
I think David Tuller would be a great speaker to suggest - he must be pretty unique in being crowdfunded by patients to tackle some bad RCTs.
After a bit of googling, I see that it was mentioned on another forum as something that Kenny de Meirleir was rumoured to be considering trying...
I thought you'd made that one up, just to catch us out! But it's real: https://en.wikipedia.org/wiki/Filgotinib I've never heard of an ME trial...
A little bump for this - I think it's on at 12:30 pm today.
It was only a couple of months ago that I found out what 'neo-liberal' actually meant, and up until that point I'd been thinking it described...
Separate names with a comma.
