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I just donated and shared it around in various places in the hope it might also help.

This is an archive from 2014 of the original co-cure website: http://web.archive.org/web/20140625035237/http://co-cure.org/ However it was mainly a mailing list and many people who used it would never have gone to this site

This now has 109 quote tweets which I think is the most ever for one of my tweets plus 141 other retweets and lots of replies. It's also popular on Facebook but more things can really take off there. I didn't mention her by name, but I don't think I'm going to be on Prof Turner-Stokes'...

Incidentally, I send a link to the Science for ME weekly update each week to Co-Cure.

For my sins, I sometimes get complaints that people can’t unsubscribe at the link including one this weekend; I am able to tell them how to unsubscribe. Also there have been some complaints that people’s messages haven’t been approved despite the fact that I don’t see their submissions. What fun.

Unfortunately I can't change the footer, nor do I think there is anyone alive who can. I did post at least one message to the list at some stage to point out that a new website had been set up at the link that wasn't associated with the list.

Before social media, mailing lists were arguably the main way information was distributed in the ME/CFS community. Co-Cure was arguably the most important list in the late 1990s and for much of the 2000's. It wasn't designed for discussion, but stand-alone posts so it was generally acceptable...

Please don't ask me to talk about thirds: it might get me in trouble! :laugh: I remember a friend from Dublin but now living in New Zealand posting how his son was wearing the 33 jersey which he figured must be deliberate!

Hopefully this World Economic Forum article hasn't been posted already? Only other reference to "post viral" that I recall:

Regarding "social mystique" :laugh:

This has already prompted a lot of discussion on Twitter. Also this response for what it is worth:

I thought I would highlight these views more widely:

Dr Strain who has a CFS clinic in Exeter mentions “chronic fatigue” towards the end.

Dr Strain who has a CFS clinic in Exeter mentions “chronic fatigue” towards the end.

https://measussex.org.uk/dr-alastair-miller-on-me-cfs-and-covid19-september/ Disappointing to see these comments on a charity website, but then this charity has been tied to the biopsychosocial approach to ME/CFS for a long time, from what I have seen.