Wuhan Coronavirus / COVID-19 Thread 2: Booster Shot - Resume all Corona sperging here.

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Sparkling Yuzu dijo:
That just shows that liberals are hypocritical but nothing about lockdowns as a public health measure.
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No. It shows that the powers that be thought people crying over some social justice issue was worth putting aside your so called public health measures. What's the point of a lockdown if a group of people are exempt for some stupid social justice issue?
 
Car Won't Crank dijo:
No. It shows that the powers that be thought people crying over some social justice issue was worth putting aside your so called public health measures. What's the point of a lockdown if a group of people are exempt for some stupid social justice issue?
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I would say that it means they knew and were aware lockdowns were stupid for covid.

The fact liberal gatherings and saw causes were fine, politicians were outed doing fun shit and parties, and the number of we were just off camera maskless gatherings of health officials mostly goes to show that they weren't ever serious about anything but power and control. Maybe money too.

If covid had been the actual serious or death sentence it was portrayed in the early days, there wouldn't be exceptions for this shit. And our glorious asshole ruling elite wouldn't have stepped out of their compounds.

And if covid had been the what..idek how high the initial death rate estimates were after the its just a cold whiplash and the diamond princess or whatever it was (also... I doubt that whiplash would have happened either. The us intelligence services knew what was up then). Anyhow if it had been that deadly and that spreadable both we would be seeing a very different reaction then and now.

Overwhelmed hospitals have far more to do with understaffed for bad nurse pay and shitty profit reasons. Hospitals now are still overwhelmed and it isnt covid. Its a broken fucking system they made worse by firing people who wouldn't take the clot shot. It was broken before covid. Muh overwhelm when remember the ships sent to new York and temp hospitals that never got a single patient? Yeah. That.
 
Sparkling Yuzu dijo:
Lockdowns were rational until the vaccine came out.
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They were not. It is irrational to force healthy people into isolation when simple measures, such as shielding the elderly and those with immune issues, is much more effective. The lockdowns did more damage to people, physically and psychologically, than exposure to corona would have.

Sweden didn't lock down its citizens and saw essentially the same outcomes as nations that did, which shows locking everyone up was not only irrational, but entirely useless.
 
Sparkling Yuzu dijo:
Lockdowns were rational until the vaccine came out.
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Lockdowns for respiratory diseases are junk science based on a politically motivated repudiation of decades worth of experience fighting similar diseases including multiple waves of pandemic flu. Same with masks.
The virus was also freely circulating for months before the alleged lab leak/spillover event in Wuhan happened in November 2019 without apocalyptic effects on excess mortality or hospital capacity.
 
While 2020 was bad in the relatively free world, it was far worse in North Korea. In response to "COVID-19" (which likely hit a malnourished population harder), they made travel inside NK harder, and they made escaping via the northern border near impossible. Also, China has more surveillance and sends defectors who escape into China back.

"How North Korea Finally Made It Impossible to Escape"
 
This shit is beyond outrageous.


Transcript of the AstraZeneca meeting audio, notes added:​

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Pascal Soriot (CEO of AstraZeneca): …[Mark] Esser [1] who has been the architect of the long-acting antibody against Covid-19. Mark, back to you. [not sure if there are two men called Mark in the meeting]

Speaker 2 [I believe that’s Mark Esser]: Excellent! So, thank you for the introduction, Mark, and it’s really a pleasure to share with all of you a little bit of the journey that the “long-acting antibody” team has taken in 2020, but actually our story begins back in 2017 in the basement of a Quality Inn in Tysons Corner VA at the Defense Department Industry Day [BARDA runs “industry days” on regular basis]. There, I met Col. Matt Hepburn, who is actually the architect of the Pandemic Prevention Program or P3, and the goal of P3 was going from the discovering a novel virus to producing drugs in less than 60 days – something that would normally take 6 years at best. To me that sounded more like science fiction than science, but we signed up in a small and committed team of virologists and molecular biologists and engineers and started working in 2018 on new technologies to discover and manufacture antibodies against viruses. The team has actually been pretty successful on the early discovery engine piece and had won a biopharma R&D award about this time last year. So, in January we were all anxiously following the emerging news from China about the new disease. It wasn’t a surprise to me when I got a call on February 4th from the Defense Department here in the US saying that the newly discovered Sars-2 virus posed a national security threat. We needed to stop everything we were doing on our model system influenza, and put everything onto Sars-2. Fortunately, our top 2 virologists, Patrick [?] were already a step ahead, having cloned and expressed the virus protein soon after the virus sequence was published on January 21st. Of course, the task was formidable: we had to learn everything we could about the new virus, the immune response to the virus, and the disease called “Covid-19”. What we and others quickly learned was that the critical protein on the virus is called the “spike protein” and this is the protein on the virus that allows the virus to infect cells by binding to the ACE-2 receptor, and what we also learned was that it could exist in active and an inactive form. In the active form it expressed a special domain called a Receptor Binding Domain, or the RBD, and what we quickly figured out was that RBD was going to be the “Achilles’ heel” of the virus. So, we decided that our best strategy was to come up with two antibodies against this Receptor Binding Domain, and we set out with a three-pronged approach to discover those antibodies. First, we tried to isolate these B-cells from the blood taken from Covid-19 patients. Second, we immunized humanized mice with different constructs of spike protein to elicit those magical B-cells, and third, we ran a huge screen using our traditional Cambridge antibody technology phage display library. All in all, we screened tens of thousands of antibodies, and then discovered about 1500 that bound the spike protein and whittled it down to our top 100 by the end of March. The team worked late into the night, weekends – their commitment was inspiring, and they surprised me with their “top 12” neutralizing antibodies on my birthday, April 10th. The next challenge was to down-select from these 12 neutralizing antibodies to our “top 2”. The best way I can describe this is like trying to put together a jigsaw puzzle while blindfolded, but at the end the team selected two very distinct, two very potent antibodies that showed synergistic activity. When I say, “synergistic activity”, it was 1% + 1% actually equaled 93% neutralization. At the same time, our protein engineers, who are in my mind are some of the best in the world, made key enhancements to the antibodies to extend their half-lives so that a single dose could afford up to 6 to 12 months of protection, ensure high yield production in 15,000 liter bioreactors, and be stable up to 1 year in a refrigerator. So, all in all, all this was done in just 99 days - 1 day ahead of schedule. So, our last hurdle to overcome was to accelerate that normal kind of 2 to 3 year early development timeline into 2 months, and we basically did that by running everything in parallel, and making significant investments at risk. Two notable examples were manufacturing of the Cho-cell pools and starting out tech transfer to our tech transfers to our manufacturing partners before we had even selected our top clones. Our clinical and regulatory teams worked around the clock, and we dosed our first patient on August 21st [2020], and I am happy to report that we started our two Phase 3 studies: PROVENT last week, and yesterday we dosed first patient in my favorite study, “Storm Chaser” yesterday. It’s really been astonishing to see how everyone in the company has pulled together and risen to the challenge, and I’ve had the good fortune working with everyone in Biopharma R&D, Precision Medicine, Legal, Business Development, Procurement, Project Management, Ops [Operations], IT [information technology], Commercial and the all-important Government Affairs, and I’d like to take this moment to thank everyone. So, clearly, fighting a virus like Sars-2 in a worldwide pandemic is not for the faint of heart, but clearly, we are all in this fight to the finish. Also, very grateful to Pascal [Soriot, the CEO], Mene (Sir Menelaus Pangalos, an AZ board member) and Nesset (sp) for their leadership, and I am very proud to be part of the company that not only follow the science but is putting patients first and doing what is right thing for the whole world. Just like the antibody we are “better together” and I look forward to being with many of you in a healthier and happier 2021. So, thank you and over to you, Pascal.

Pascal Soriot: Thank you, Mark, and congratulations again to you and the team. This long-acting antibodies are quite unique because this is the only combination that potentially will last more than 6 months, up to potentially 12 months and protect people for a long period of time. And for those of you who may not be totally familiar with antibodies, you know, you have to know a number of people cannot be vaccinated, like if you have an immune disease, lupus or some other immune condition… or multiple sclerosis, you cannot be vaccinated. So, there are millions of people in the world that will need the protection that cannot be coming from a vaccine, so the long-acting antibody has the enormous potential.
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https://twitter.com/wolsned/status/1753707976286679166 (Mirror: https://rumble.com/v4boejt-mark-sexton-on-pfizer-contract-with-south-african-government.html)


https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452662/ - https://archive.md/V2rPi

The COVID-19 pandemic caused much illness, many deaths, and profound disruption to society. The production of ‘safe and effective’ vaccines was a key public health target. Sadly, unprecedented high rates of adverse events have overshadowed the benefits. This two-part narrative review presents evidence for the widespread harms of novel product COVID-19 mRNA and adenovectorDNA vaccines and is novel in attempting to provide a thorough overview of harms arising from the new technology in vaccines that relied on human cells producing a foreign antigen that has evidence of pathogenicity. This first paper explores peer-reviewed data counter to the ‘safe and effective’ narrative attached to these new technologies. Spike protein pathogenicity, termed ‘spikeopathy’, whether from the SARS-CoV-2 virus or produced by vaccine gene codes, akin to a ‘synthetic virus’, is increasingly understood in terms of molecular biology and pathophysiology. Pharmacokinetic transfection through body tissues distant from the injection site by lipid-nanoparticles or viral-vector carriers means that ‘spikeopathy’ can affect many organs. The inflammatory properties of the nanoparticles used to ferry mRNA; N1-methylpseudouridine employed to prolong synthetic mRNA function; the widespread biodistribution of the mRNA and DNA codes and translated spike proteins, and autoimmunity via human production of foreign proteins, contribute to harmful effects. This paper reviews autoimmune, cardiovascular, neurological, potential oncological effects, and autopsy evidence for spikeopathy. With many gene-based therapeutic technologies planned, a re-evaluation is necessary and timely.
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(Mirror: https://rumble.com/v4c1u0t-dr.-john-campbell-what-are-these.html)
 
ToroidalBoat dijo:
While 2020 was bad in the relatively free world, it was far worse in North Korea. In response to "COVID-19" (which likely hit a malnourished population harder), they made travel inside NK harder, and they made escaping via the northern border near impossible. Also, China has more surveillance and sends defectors who escape into China back.

https://youtube.com/watch?v=jlX7tl1QvJs"How North Korea Finally Made It Impossible to Escape"
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That is going to be a lot of countries if they sign The Pandemic Treaty. Surveillance and travel restrictions like you won't believe.
 
Ugh, now that Piñera died, everyone his sucking his dick about "HOW WELL HE MANAGED ZE COOF WE WOULD ALL BE DEAD IF WE HAD ANOTHER PRESIDENT DURING THE PERIOD BUT HE DID THE IMPOSSIBLE AND FORCED THE WHOLE COUNTRY TO SHUT THEMSELVES AT THEIR HOMES, MASK UP AND GET THE SHOTS SO CHILE'S THE MOST JABBED COUNTRY EVER AND THAT'S SO GOOD THAT HE GOT PRAISED INTERNATIONALLY FOR HIS GESTION!!!!" That's a bad thing you bunch of niggercattle idiots, he was the most globohomo trash that ever globohomo'd, the consequences are showing, everyone is getting cancer or some other weird shit that ends up disabling people, but what matters is that grandma got saved, right?
 
The topic of people being ill came up in a conversation with family last night. Anecdotally, the number of people getting pneumonia is through the roof (dad even said as much - he's worried about getting it at his age, so he pays attention), based on how many people they know who have had it in the last month or two. They each mentioned several different people and each know at least one who was so ill that a hospital visit was necessary. Nobody said anything about the rona or vaccinations, which was a change from the usual way these conversations go.
 
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