What can be done by us, in terms of public statements and contacting the relevant professional bodies, to protect these post-Covid patients...
My understanding is that this - each of many mutations raising risk slightly - is the norm for many diseases and the idea is to identify the...
More stories in The Times today (which Andy is posting on other threads). Whenever a story allow comments, we should be posting the link to the...
If there is a comments section, I'd address the sane audience over the heads of the trolls and I'd paste the link for patients and supporters to...
Cobbled together from that Facebook post: [IMG][IMG][IMG]
This is excellent!
There's an MEpedia page on it here. It only mentions the MTHFR mutation, though.
You can see it in Andy's post that I linked to. Whipple's piece is the last one on that page.
From the FAQs page: CureME will apply its diagnostic algorithm (a very specific set of rules) to assess people according to well accepted...
Sorry - I edited the link and it should be OK now.
No pressure, no pressure....
Thank you, Chris! This has been a brilliant day for all of us. I've waited more than 30 years for serious, large-scale science like this. I can't...
Oops! Thanks - I've edited that link.
Scroll to the bottom of Andy's post to see it full-size. (Link edited - thanks, @lunarainbows!)
The amazing DecodeME ME/CFS DNA project that just got funded, is holding a webinar on 6 July. Details to be announced later, presumably - this...
By government - the MRC and NIHR are government-funded.
@Andy - I still haven't received an email but gather from someone who has that it says that the study’s Management Team will host a Q&A webinar at...
Maybe one for the FAQs, @Andy - is it likely that post-corona patients are likely to get a 'post-coranavirus sydrome' diagnosis rather than an...
Numbers going up! [MEDIA]
I'm confused. Surely the point of getting those early sign-ups was so that they'd be permanently on the mailing database (unless they asked to be...
Separate names with a comma.
