... RaTG13 and other bat CoVs from the same deadly Yunnan cave fitting the stated inclusion rule for use in the hACE2-optimized recombination grant, SARS-CoV-2 indeed binding human ACE2 hundreds of times better than SARS-CoV, winter in a city outside known ranges of such bats,
... fully synthetic recombination techniques and full genome data already available, prior use of non-SARS-CoV backbones and a clear justification for doing so again, a demonstrated history of refusing to disclose sequences and lying about both culture work and deadly pathogens,
... ground zero a human superspreader event at a market down the highway from the WIV CAS office and a few hundred meters from the Wuhan CDCP, *right around a biosafety conference with staff from the BSL3/4 lab* known to be infecting animals at the time.
One was likely sick and simply didn't know it yet, and that is all that would have been required.
The furin site facilitates pre-symptomatic spread, contrary to SARS-CoV which lacked one. It confused the WHO and national authorities. The lab likely didn't quarantine for it.
Removed one post, rephrased:
Multiple demonstrable lies from Shi.
Appointment of Daszak himself to lead the Lancet commission on COVID-19 origins (absurd conflict of interest), rapid statement against (his own) lab involvement.
This swapping of Spike proteins and even small manually selected mutations has extensive precedent within the SARS-family CoV ecological research community.
Congressional representatives noted concerns raised by the EcoHealth bat coronavirus grant work ongoing in Wuhan as well.
This is consistent with the broader documented pattern of hiding samples and sequence data, and lying about the extent of experiments performed.
Interview with Baric, in which he states as expected that the fully synthetic methods used in his chimeric SARS-like virus work with EcoHealth do not leave any particular genetic signature at all.
- decide what the word "evidence" means:
a) "clinical results with appropriate sample(s) and endpoints"
b) "what huge lumbering institutions claim ex cathedra with no citations"
c) "what gilead et al. claim"
d) "peer best practices"
- take low-risk bets
If in doubt, *ask the patient*.
People have a fundamental right to participate in their own health-- *they already do so 99% of the time anyway*.
'This might help with X; it's a bit less certain; may cause Y side effects; studies say usually well-tolerated; do you want to try?'
The continued failure to trial or use ITPP in critical care is an indictment against the regulatory and productive institutions of our supposedly-advanced (increasingly just shorthand for 'gridlocked') economy.
Thousands of people already use it for athletic activities.
It has no side effects, is safe at huge doses in animal studies, and has never had a serious adverse event reported in the community ('that's informal' it's post-marketing surveillance..).
The fact that we are jamming tubes down people's throats before giving this, or for that matter even giving cyproheptadine, absolutely disgusts and appalls me.
>Oh that isn't proven
Yes. It. Is.
READ A BOOK; THEY ARE BOTH LITERALLY BASIC PHYSIOLOGY.
>One hope is that the efficacy of the Johnson & Johnson vaccine could rise if it is given as a two-dose regimen.
Obviously, yes! This is much more promising.
Single-dose frankly seems gimmicky, in a very specific sense:
This is effectively just offloading the debate about whether to halfway-dose existing vaccines to a new vaccine candidate instead-- one that has actually been trialed in this dosing schedule.
A couple things about which I would like to be clear, from the now-big account (likely smaller over time):
1) do not ever @/DM to ask where I am or act like I owe you something-- pay me a bitcoin if you want that kind of attention, I know that is pocket change to some of you
2) I have a life outside of COVID-19 and a very, very detailed post history that is approximately two clicks away, depending on your choice of platform access method: search feature, "__ice9 <whatever topic>" papers generally do not become 'out of date' and a result is a result
3) I am frankly a bit bored. The acute disease was obviated months ago by dual entry inhibition. Not my problem if the west ignored it because it came from Iran, or due to statistical illiteracy or vile conflicts of interest (hi Gilead puppets 🎭). Fluvoxamine looks great too.
Side note: strangely demanding PK study; very rigorous protocol. Hope participants were at least paid well. But they got us a number so I am pleased.
NAC may not have a large impact in monotherapy, given only EC50 is hittable (not EC90 except perhaps IV) and gappiness in plasma concentration peaks even q.i.d. (slightly compensated by permanent nature of damage done to exposed Spike copies).