The CDC's new mask (or unmask) guidance means I am supposed to trust that people who for over 14 months have been denying the science and not taking precautions will now be responsible and honest about their vaccination status?
Additional background - The group that conducted this systematic review for the CDC is the same one that did the systematic review for AHRQ before the P2P meeting in 2014.
https://effectivehealthcare.ahrq.gov/products/chronic-fatigue/research-protocol...
Yet there were trials of monoclonal antibodies for acute COVID19. NIH (and other agencies) can innovate for COVID19 (and longCOVID) but when it comes to ME, nope.
This article is also mentioned in another thread https://www.s4me.info/threads/possibility-of-me-or-pvfs-after-covid-19-long-covid.14074/page-176#post-325652
The document on treatment is likely to take a while since CDC hasn't finished its review of the treatment evidence review they contracted for. (It is due out at any time for public comment.)
Not every ME patient gets PEM from cognitive exertion. (Though most PwME I know, do get PEM from cognitive exertion.) I suspect that measuring cognitive exertion is not as convincing (visible) as physical exertion and might be more open to
@Creekside some of the people who are qualified to do a 2 day CPET for PwME will do cognitive assessments before and after testing to add to reports. This assesses (of course) both cognitive and physical impact of exertion.
I don't think there's been enough work on cognitive exertion and PEM...
I apologize if this has already been posted (mentions me/cfs in section 3.1 but sadly includes no links)
https://www.sciencedirect.com/science/article/pii/S030439402030803X?via%3Dihub
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