Pandemic threat? Anyone else concerned?

I remember the panic about the "Delta" variant. Hair on fire, full panic mode and MSM in a tizzy. What happened to the "Delta" variant? We're all still here, for the most part other than the normal death rates we've seen previously, and even those are going down.

Does this sound familiar?
A Fearful Population is easier to control.
 


Much has been made of the news that Joe Biden has shut the door to eight countries over the new 'omicron' COVID variant. AT deputy editor Andrea Widburg has an excellent piece today on that here.

Some of the implications, of course, are vaguely comical. Biden's White House medical advisor, Dr. Anthony Fauci, the so-called "expert" and voice of "science" he touted was last seen recommending against the closure of air travel.

Joe, of course, did it anyway, signaling that Fauci's expertise to him is all about what's politically useful and, apparently, this wasn't.

There's just one problem with all this purported concern from Biden about the variant and tune-changing:

He hasn't said a thing about the wide-open border.

In fact, he's still leaving the border open to all comers.
Thus far, he has said nothing about shutting the border, which this year has seen a record 1.6 million illegal "border encounters" into the U.S. in the past year, a record high, with tens of thousands more on their way.
 
If you weren't already convinced, you double your risk of cardiac incidents and the rate of stillborn babies is up by 29 times (but only if you are vaccinated). Does anyone in authority care?

I’m getting a lot of people telling me about this abstract that appeared in Circulation, which is arguably the top-rated journal on cardiology. This was incorporated in my latest slide deck (slide 26 and 27 at the time this is being written). Yes, this is a big deal. But nobody is listening. Cardiac risk could go up 1,000X after vaccination and it wouldn’t matter. Nobody is listening. This article is proof of that.

Here’s the punch line from the abstract:
These changes resulted in an increase of the PULS score from 11% 5 yr ACS risk to 25% 5 yr ACS risk. At the time of this report, these changes persist for at least 2.5 months post second dose of vac. We conclude that the mRNA vacs dramatically increase inflammation on the endothelium and T cell infiltration of cardiac muscle and may account for the observations of increased thrombosis, cardiomyopathy, and other vascular events following vaccination.

Stillborn babies

The punchline here:
There is a 29X increase in the rate of stillborn babies in Waterloo, Ontario that started after vaccination program rolled out. All the mothers of the stillborn babies were vaccinated. I’m sure this is happening everywhere, but nobody in the US wants to lose their job over this.

So why the CDC is saying this is perfectly safe for pregnant women? I’m curious as to what the CDC has determined the cause of this. Obviously, it couldn’t be the “safe and effective” vaccine. Note: the CDC doesn’t have jurisdiction in Canada of course, but they could call over there and find out… The good news of course is that this only appears to be happening in areas of the world where they release data to the public on what is going on.

One place is Scotland: Investigation launched into abnormal spike in newborn baby deaths in Scotland. This only started post-vaccine and I bet that all the moms were vaccinated. Isn’t it odd that they don’t list the vax status of the moms? Another place is Canada, but only thanks to a courageous whistleblower (otherwise, we wouldn’t know):

https:/stevekirsch.substack.com/p/latest-devastating-news-on-the-vaccine
 
Interesting read from Science Magazine.

'Patience is crucial': Why we won't know for weeks how dangerous Omicron is

At 7.30 a.m. on Wednesday, Kristian Andersen, an infectious disease researcher at Scripps Research in San Diego, received a message on Slack: “This variant is completely insane.” Andrew Rambaut of the University of Edinburgh was reacting to a new SARS-CoV-2 genome sequence found in three samples collected in Botswana on 11 November and one picked up a week later in a traveler from South Africa to Hong Kong.

Andersen looked at the data and then replied: “Holy shit—that is quite something. The length of that branch...” A few minutes later he added: “Just had a look at the list of mutations—so nuts.”

They were talking about what is now called Omicron, a new variant of concern, and the long branch Andersen noticed refers to its distance to every other known virus on SARS-CoV-2’s evolutionary tree. The variant seemed to have picked up dozens of mutations, many of them known to be important in evading immunity or increasing transmissibility, with no intermediate sequences in the database of millions of viral genomes. On Tuesday, after spotting the odd sequences in a global database, Tom Peacock, a virologist at Imperial College London, had already posted his own verdict on GitHub: “This could be of real concern.”

Now, once again, the world is watching as researchers work nights and weekends to learn what a new variant has in store for humanity. Is Omicron more infectious? More deadly? Is it better at re-infecting recovered people? How well does it evade vaccine-induced immunity? And where did it come from? Finding out will take time, warns Jeremy Farrar, the head of the Wellcome Trust: “I'm afraid patience is crucial.”

Researchers in South Africa were already on the trail of this new variant. Several teams were independently trying to figure out why cases were spiking in Gauteng, a northern province that includes Johannesburg and Pretoria. And a private lab called Lancet had noticed that routine PCR tests for SARS-CoV-2 were failing to detect a key target, the S gene, in many samples, a phenomenon previously seen with Alpha, another variant of concern. When Lancet sequenced eight of these viruses, they found out why: The genome was so heavily mutated that the test missed the gene.

Lancet shared the genomes with the Network for Genomics Surveillance in South Africa (NGS-SA), which called an urgent meeting on Tuesday. “We were shocked by the number of mutations," says Tulio de Oliveira, a virologist at the University of KwaZulu-Natal and NGS-SA 's principal investigator. After the meeting, de Oliveira says, he called South Africa's Director General of Health and "asked him to inform the minister and president that a potential new variant was emerging." The team sequenced another 100 randomly selected sequences from Gauteng in the next 24 hours. All showed the same pattern. After informing the government, de Oliveira and his colleagues presented their evidence at a press conference on Thursday morning. On Friday, the World Health Organization (WHO) designated the virus a “variant of concern” and christened it Omicron. (Variant names follow the Greek alphabet but WHO skipped the letters Nu and Xi, it said, “because Nu is too easily confounded with 'new' and Xi was not used because it is a common surname.“)

One reason for concern about Omicron is that sequenced samples indicate it has rapidly replaced other variants in South Africa. But that picture might be skewed. For one, sequencing might have been focused on possible cases of the new variant in recent days, which could make it appear more frequent than it is. PCR data provide broader coverage and a less biased view, but there too, samples with the S gene failure indicate a rapid rise of Omicron.

But the rising frequency could still be due in part to chance. In San Diego, a series of superspreading events at a university resulted in an explosion of one particular strain of SARS-CoV-2 earlier this year, Andersen says: "It was thousands of cases and they were all the same virus.” But the virus wasn't notably more infectious. South Africa has seen relatively few cases recently, so a series of superspreading events could have led to the rapid increase of Omicron. “I suspect that a lot of that signal is explained by that and I desperately hope so,” Andersen says. Based on a comparison of different Omicron genomes, Andersen estimates that the virus emerged sometime around late September or early October, which suggests it might be spreading more slowly than it appears to have.

The other reason to be concerned is Omicron's confusing genome. Its spike protein, which latches on to cells on human receptors, has 30 amino acid differences from that of the original Wuhan virus. In addition, amino acids have disappeared in three places and new ones appeared in one place. (Other proteins too, have undergone changes.) Many of the changes in spike are around the receptor binding domain, the part of the protein that makes contact with the human cell. “That is very troubling,” Farrar says. Structural biology mapping last year showed that some of these changes made the virus bind to the receptor much better.

It’s hard to tell how infectious a virus is based on mutations alone, says Aris Katzourakis, an evolutionary biologist at the University of Oxford. “But if we were looking out for mutations that do affect transmissibility, it's got all of them,” he says.

The sequence also suggests the virus could excel at evading human antibodies, says Jesse Bloom, an evolutionary biologist at the Fred Hutchinson Cancer Research Center. The human immune system produces a host of different antibodies that can neutralize SARS-CoV-2, but many of the most important ones fall into three categories that each target a slightly different site on the spike protein of the virus, simply called 1, 2 and 3. A mutation called E484K has long been worrying because it changes the shape of the site that class 2 antibodies recognize, making them less potent. Omicron carries this mutation and similar changes in the sites for the other two classes of antibodies.

Bloom thinks people who recovered from COVID or were vaccinated are unlikely to completely lose their ability to neutralize the virus. “But I would expect, based on this particular combination of mutations, that the drop in neutralization is larger than for all the other major variants.”

Experiments in the laboratory will have to show whether he is right. Alex Sigal, an infectious disease researcher at the Africa Health Research Institute, says he received swabs with Omicron on Wednesday and has started to grow the virus. Producing enough of it to test against sera from vaccinated and recovered individuals will take a week or two, he says. Other researchers will test viruses genetically engineered to carry just the spike protein of Omicron, a process that is faster than growing the variant itself but a bit further removed from what happens in real life.

As such studies take place, it's crucial to closely monitor any shifts in the pandemic, Farrar says. “Do you see cases increasing not just in South Africa but the broader South African region?” The virus has already been picked up in Belgium, the United Kingdom, and Israel, Farrar points out, and will probably be found elsewhere as well. “Do you see transmission increasing in other parts of the world around presumed index cases?” Epidemiologists will also watch for changes in disease severity—how many people are hospitalized and die. All that will take time.

In the meantime, the European Union, the United States, and many other countries have restricted travel to and from southern Africa in a bid to protect themselves. Travel restrictions are unlikely to stop the variant, Farrar says, but they can buy some time. “The question is what you then do with the time.”

Travel restrictions come with an economic and social cost, which could be a disincentive to report new variants. “I've heard through the grapevine that countries didn't push sequences out very quickly [in the past] because they were worried about travel bans,” says Emma Hodcroft, a virologist at the University of Bern. “This is the opposite of what we want.”

Such considerations did not stop South African researchers, de Oliveira says. “We do risk a massive backlash in case [Omicron] does not cause a massive wave of infection and can be controlled,“ he wrote in a message. "But this is a risk that I am comfortable to live with as the pandemic has caused so many deaths and suffering. [Our] hope is that our early identification will help the world.“

 
FINALLY
FAUCI RELEASED THE NEW END BOSS


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I just began reading Robert F. Kennedy, Jr's book 'The Real Anthony Fauci'. The very first thing is this quote in the introduction:

“The first step is to give up the illusion that the primary purpose of modern medical research is to improve Americans’ health most effectively and efficiently. In our opinion, the primary purpose of commercially funded clinical research is to maximize financial return on investment, not health.”

—John Abramson, M.D., Harvard Medical School
 
I just began reading Robert F. Kennedy, Jr's book 'The Real Anthony Fauci'. The very first thing is this quote in the introduction:

“The first step is to give up the illusion that the primary purpose of modern medical research is to improve Americans’ health most effectively and efficiently. In our opinion, the primary purpose of commercially funded clinical research is to maximize financial return on investment, not health.”

—John Abramson, M.D., Harvard Medical School
and thus, the Corruption of Medicine is complete....
 
LMFAO, the WHO doesn't want altercation with Winnie the Pooh, but wait...WHO is Xi Jinping



WHO Likes Propaganda? Yum Yum

 
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So it’ll be everywhere this coming week.

I see one talking head with the World Health consortium saying it’ll be as bad as Ebola, and another doc from SA saying it’s a nothing burger.

So do I buy more toilet paper or 5.56? :idk:

(jk. I have plenty of 5.56 ;)
 
So it’ll be everywhere this coming week.

I see one talking head with the World Health consortium saying it’ll be as bad as Ebola, and another doc from SA saying it’s a nothing burger.

So do I buy more toilet paper or 5.56? :idk:

(jk. I have plenty of 5.56 ;)
plenty of 5.56????
1638123163362.png


I missed out on buying more before prices went bonkers. Have less than 500 rounds now... booo.