I did this, although it took me a lot longer than 15 minutes. It's interesting; NICE seems to be testing out providing more information related to recommendations, and how the information is laid out.
The example recommendation they gave for comment included a short sentence saying it was...
:rofl: just 'presenting' it at all would be a start.
I would suggest that, for any recommendations of treatment or advice to be given to patients, there should be a statement about what level of evidence there is.
My understanding is that there is some sort of code in the guideline language...
(Just thinking ahead, BAME isn't great as many would pronounce it 'barmy'.
If they went for BAM, it would look great on the current front page of the website, especially with an exclamation mark, BAM!)
It would be great if that happened (at least, the UK members of those organisations).
It's not very clear to me who can join, but it looks as though anyone 'with a specific interest in CFS/ME' can.
This is what I came here for:
The following statement from (or at least attributed to) BACME has been posted and discussed on the guideline delay thread:
I was just checking out the BACME website.
I've included the front page here just in thumbnail, because I don't want to inflict it on you if you aren't feeling up to it.
I can not think of a less appropriate front page for a professional website related to ME/CFS. I mean, on another page...
No, most of the over-hyped studies come out of Griffiths University. Daniel is a member here and has taken the time to engage with us. He is part of a team that has done interesting work on mitochondrial dysfunction. We have looked at some of their published studies.
(click on the missailidis...
I was idly googling and found this interesting tribute by a charity, Validity, based in Hungary focused on mental health advocacy, but clearly working in Bulgaria and very connected to the disability rights movement there.
https://validity.ngo/2017/03/09/a-tribute-to-rusi-stanev/
Validity...
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