Dec 242021
 


Claude Monet Camille Sitting on the Beach at Trouville 1870-71

 

Vaccine Effectiveness Against Infection With Omicron Or Delta (medRxiv)
UK Reveals How Long Boosters Protect From Omicron (RT)
Efficacy And Safety Of Two Neutralising Monoclonal Antibody Therapies (Lancet)
The Mask and the Face (Farrow)
Patriotic Duty My Eye (David Stockman)
If You’ve Had COVID You’re Likely Protected for Life (Mercola)
Ontario List Fluvoxamine As A Covid-19 Treatment To Consider (CTV)
A Myth is Born: How CDC, FDA, and Media Wove a Web of Ivermectin Lies (Resc.)
‘Biden Seems Confused’: CNN Question President’s Cognitive Health (DM)
Fauci et al Withheld Information on China’s Coronavirus Experiments (NW)
US Airlines Cancel Hundreds Of Flights Scheduled For Friday (DM)
Putin Reveals Thinking Behind 2014 Moves In Crimea (RT)

 

 

 

 

 

 

Brian Tyson: 70% of deaths could have been saved with early treatment. I have not lost a single patient (of over 6,000).

 

 

When a T cell is exposed to a foreign pathogen, it extends a signaling device or ‘antenna’ known as a vitamin D receptor. It then searches for vitamin D. If there is an inadequate vitamin D level, they won’t begin to mobilize.

 

 

“..but deaths continue to climb”. That’s what the FT gets from this series of graphs. Good grief.

 

 

 

“This study shows that after three months the vaccine effectiveness of Pfizer & Moderna against Omicron is actually negative. Pfizer customers are 76.5% more likely and Moderna customers are 39.3% more likely to be infected than unvaxxed people. “

“Observational study from Denmark indicates that the mRNA vaccines protect for a few weeks only but then SIGNIFICANTLY AUGMENT Omicron infectivity. Is the immune system actually harmed, creating shot repetition dependency (with unknown long-term safety)?”

Vaccine Effectiveness Against Infection With Omicron Or Delta (medRxiv)

In this brief communication we are showing original research results with early estimates from Danish nationwide databases of vaccine effectiveness (VE) against the novel SARS-CoV-2 Omicron variant (B.1.1.529) up to five months after a primary vaccination series with the BNT162b2 or mRNA-1273 vaccines. Our study provides evidence of protection against infection with the Omicron variant after completion of a primary vaccination series with the BNT162b2 or mRNA-1273 vaccines; in particular, we found a VE against the Omicron variant of 55.2% (95% confidence interval (CI): 23.5 to 73.7%) and 36.7% (95% CI: -69.9 to 76.4%) for the BNT162b2 and mRNA-1273 vaccines, respectively, in the first month after primary vaccination. However, the VE is significantly lower than that against Delta infection and declines rapidly over just a few months. The VE is re-established upon revaccination with the BNT162b2 vaccine (54.6%, 95% CI: 30.4 to 70.4%).


Note the number of cases in this stat:

Read more …

10 weeks. That’s it. Leave the needle in.

Or: realize that Omicron is a very mild version of a disease that 99.97% of people already survived, and keep the needle out forever.

Because after 12 weeks (3 months), see above, “Pfizer customers are 76.5% more likely and Moderna customers are 39.3% more likely to be infected than unvaxxed people. ”

UK Reveals How Long Boosters Protect From Omicron (RT)

While Covid-19 booster shots provide more protection against severe disease from the new Omicron variant, even this starts to wane after 10 weeks, the UK Health Security Agency has announced amid talk of post-Christmas lockdowns. The agency’s data on Omicron in comparison to the previously dominant Delta variant of the virus shows that people infected by the new strain may be up to 70% less likely to end up in a hospital, UKHSA Chief Executive Jenny Harries said on Thursday. She called it an “encouraging early signal” but noted that “this is early data and more research is required to confirm these findings.” Health Secretary Sajid Javid welcomed the findings, but pointed out that “cases of the variant continue to rise at an extraordinary rate – already surpassing the record daily number in the pandemic.”


“Hospital admissions are increasing, and we cannot risk the NHS [National Health Service] being overwhelmed,” Javid said. Protecting the NHS was the rationale for the original 2020 lockdown, based on the early doomsday models from Professor Neil Ferguson at Imperial College in London. Addressing widespread speculation about new restrictions coming after the holidays, Javid said it was “still too early” to tell and that the government was continuing to “monitor the data hour by hour.” He urged Britons to “please stay cautious this Christmas and get your booster as soon as possible to protect yourself and your loved ones.” “While two doses of the vaccine aren’t enough, we know boosters offer significant protection against the variant and early evidence suggests this strain may be less severe than Delta,” the minister said. However, UKHSA data noted that the booster efficacy begins to wane more quickly against Omicron, and is already 15-25% lower after just 10 weeks.

Read more …

Hmm. Panacea?

Efficacy And Safety Of Two Neutralising Monoclonal Antibody Therapies (Lancet)

Findings Between Dec 16, 2020, and March 1, 2021, 546 patients were enrolled and randomly assigned to sotrovimab (n=184), BRII-196 plus BRII-198 (n=183), or placebo (n=179), of whom 536 received part or all of their assigned study drug (sotrovimab n=182, BRII-196 plus BRII-198 n=176, or placebo n=178; median age of 60 years [IQR 50–72], 228 [43%] patients were female and 308 [57%] were male). At this point, enrolment was halted on the basis of the interim futility analysis. At day 5, neither the sotrovimab group nor the BRII-196 plus BRII-198 group had significantly higher odds of more favourable outcomes than the placebo group on either the pulmonary scale (adjusted odds ratio sotrovimab 1·07 [95% CI 0·74–1·56]; BRII-196 plus BRII-198 0·98 [95% CI 0·67–1·43]) or the pulmonary-plus complications scale (sotrovimab 1·08 [0·74–1·58]; BRII-196 plus BRII-198 1·00 [0·68–1·46]).

By day 90, sustained clinical recovery was seen in 151 (85%) patients in the placebo group compared with 160 (88%) in the sotrovimab group (adjusted rate ratio 1·12 [95% CI 0·91–1·37]) and 155 (88%) in the BRII-196 plus BRII-198 group (1·08 [0·88–1·32]). The composite safety outcome up to day 90 was met by 48 (27%) patients in the placebo group, 42 (23%) in the sotrovimab group, and 45 (26%) in the BRII-196 plus BRII-198 group. 13 (7%) patients in the placebo group, 14 (8%) in the sotrovimab group, and 15 (9%) in the BRII-196 plus BRII-198 group died up to day 90.

Interpretation Neither sotrovimab nor BRII-196 plus BRII-198 showed efficacy for improving clinical outcomes among adults hospitalised with COVID-19.

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Douglas Bryce Farrow, Professor of Theology and Ethics, McGill, Montréal.

“Yet here we are: masked, isolated, feastless and party-less, sent back online to begin winter term, because this response to COVID has proved the abject failure that honest scientists warned from the outset it would be.”

The Mask and the Face (Farrow)

Dear […] Thank you for responding on behalf of the provost, and for passing on the congratulatory letter to our students from the city’s director of Public Health. As you know, in any McGill communication I receive, I don’t read past the point where it begins offering me unsolicited medical advice, which is beyond the university’s competence and which I have made clear I regard as a form of harassment. But this letter, being from an external bureaucrat, I read through with some interest. I was struck by this line: “La vaccination demeure le geste civique le plus efficace pour préserver nos acquis de cet automne.” “Vaccination remains the most effective civic gesture to preserve our achievements this autumn.” What remarkable transparency and simplicity!

Vaccination—or, more accurately, an experimental injection with lipid nanoparticles of uncertain and possibly toxic effect on bodily tissues, used as a delivery system for genetic instructions designed to reprogram certain cells so as to cause them to produce an unknown quantity of a spike-protein pathogen with equally uncertain, but certainly dangerous, effects on the immune system and on other crucial systems, circulatory, nervous, reproductive, etc.—has, mirabile dictu, become le geste civique. Then again, what else could it become? For plainly it has not become a means of prevention of the spread of a coronavirus, even allowing (as I do not) that preventing spread is a rational and achievable goal. The latest iteration of the virus appears, if anything, to prefer the vaccinated.

Isn’t that convenient? Omicron is highly transmissible but not very severe, so according to the new definition of a “pandemic,” onwards and upwards with pandemic measures! Perhaps the achievement of which Dre. Drouin speaks, then, is merely that of putting the first two needles in every arm, as a prelude to the many more that are to come? With your help, she’s certainly done well with that. Yet here we are: masked, isolated, feastless and party-less, sent back online to begin winter term, because this response to COVID has proved the abject failure that honest scientists warned from the outset it would be. The Great Reset—sorry, the dangerous pandemic—rolls on, with no end in sight. One of your administrative colleagues at a nearby university told some of her professorial charges, who had expressed concern about the psychological and pedagogical well-being of their students, to expect three or four more years of this. I hope there will be some annual variation in the congratulatory note, particularly as the needle count rises and morale drops still more precipitously.

COVID vaccination was always primarily a civic gesture, of course, for it was never medically justified or justifiable for the majority of people, especially young people like our students. That this gesture has been elicited from the latter by manipulation, censorship, bullying and in some sectors coercion, not only of adults but now even of young children, requires one to ask what sort of gesture it really is and what kind of civic life it points toward. So does the fact that, together with associated policies such as lockdowns and denials of early treatment, it has plainly done far more harm than good. You do know, I trust, that in far too many cases the harm was permanent or fatal. That (as FOIA requests have confirmed) is something that was known to Pfizer from early days, and to the regulatory agencies by, at the latest, three months into the rollout.

Read more …

The death rate last week of 1.64 per million was down by a god-is-apparently-smiling 91%

Patriotic Duty My Eye (David Stockman)

Rough Rider Teddy must be rolling in his grave as he looks down upon these poseurs gathered in the Roosevelt room. For crying out loud, every one of them is double vaxxed and totally boosted. And they have issued orders to force the same upon more than 130 million of their countrymen—allegedly to prevent the latter from becoming walking vectors of disease and killers of their neighbors. Yet if the Vaxx is actually a spread stopper, why do they sit there in their masks? What’s the need to protect Biden from Fauci when the sainted doctor is armed to the teeth with vaxxed-in antibodies? And why is Biden festooned with the medical equivalent of Depends when he’s already got the accident-prevention protection of the Vaxx?

Or does he? That is to say, if it doesn’t work to stop the spread, the benefit is only private and not public and hence there is no earthly reason for mandating it against the will of millions of citizens who fear that the risks outweigh the benefits. And if it does stop the spread—despite the manifest evidence to the contrary—-why all the face mask virtue signalling on live TV? In short, this “photo op” is worth a thousand words. It’s a live action illustration of what’s been wrong since the beginning in March 2020. Namely, the predicate that one-size-fits all social control mechanisms—lockdowns, closures, distancing, masking, vaxxing—must be preemptively and harshly employed by arms of the state in order to stop the spread of an aerosolized airborne virus which cannot be seen and cannot be stopped.

Indeed, the latest argument for mandatory vaxxing—-that it prevents not transmission and infection but just a serious course of the disease—makes the picture patently absurd. What are these cats afraid of then? The real contagion at loose in the world—especially among the western nations which noisily congratulate themselves as model liberal democracies to be emulated by the more benighted nations inhabiting the purported darker corners of the planet—is a virulent outbreak of statist authoritarianism. That is, a definitely not Black Plague virus of the type that has challenged mankind o’er the ages has become a universal excuse for the wholesale cancellation of civil liberties and property rights like never before—even in times of world war.

Take the pathetic case of the United Kingdom. It is governed by a Conservative Party that’s traitorous to the cause of liberty and led by an unkempt Donald Trump wanna be who has assaulted the essence of liberal democracy to such a sweeping extent that his most authoritarian predecessors (i.e. Winston Churchill, among others) scarcely dreamed of it and the Donald himself couldn’t hold a candle to it. BoJo, in fact, is right now hauling out all the tools of public health authoritarianism in response to what amounts to a run-of-the-mill winter flu among the British population. And that latter proposition is not debatable. Not when you compare the peak January data, when virtually no one was vaccinated compared to 80% of adult Brits today, with the 7-day rolling averages through last week. Thus,

The case rate last week was 1,138 per million or 30% higher than the 875 per million recorded at the January 2021 peaks, but–
The death rate last week of 1.64 per million was down by a god-is-apparently-smiling 91% compared to the 18.21 rate at the January 2021 peak.

Read more …

“..immune memory to many viruses and vaccines is stable over decades, if not for a lifetime.”

If You’ve Had COVID You’re Likely Protected for Life (Mercola)

If you’ve had COVID-19, even a mild case, major congratulations to you as you’ve more than likely got long-term immunity, according to a team of researchers from Washington University School of Medicine. In fact, you’re likely to be immune for life, as is the case with recovery from many infectious agents — once you’ve had the disease and recovered, you’re immune, most likely for life. The evidence is strong and promising, and should be welcome and comforting news to a public that has spent the last year, 2020, in a panic over SARS-CoV-2. Increasingly evidence is showing that long-lasting immunity exists. Seasonal coronaviruses, some of which cause common colds, yield only short-lived protective immunity, with reinfections occurring six to 12 months after the previous infection.

Early data on SARS-CoV-2 also found that antibody titers declined rapidly in the first months after recovery from COVID-19, leading some to speculate that protective immunity against SARS-CoV-2 may also be short-lived. Senior author of the study, Ali Ellebedy, Ph.D., an associate professor of pathology and immunology at Washington University School of Medicine in St. Louis, pointed out that this assumption is flawed, stating in a news release: “Last fall, there were reports that antibodies waned quickly after infection with the virus that causes COVID-19, and mainstream media interpreted that to mean that immunity was not long-lived. But that’s a misinterpretation of the data. It’s normal for antibody levels to go down after acute infection, but they don’t go down to zero; they plateau.”

The researchers found a biphasic pattern of antibody concentrations against SARS-CoV-2, in which high antibody concentrations were found in the acute immune response that occurred at the time of initial infection. The antibodies declined in the first months after infection, as should be expected, then leveled off to about 10% to 20% of the maximum concentration detected. In a commentary on the study, Andreas Radbruch and Hyun-Dong Chang of the German Rheumatism Research Centre Berlin explained: “This is consistent with the expectation that 10–20% of the plasma cells in an acute immune reaction become memory plasma cells, and is a clear indication of a shift from antibody production by short-lived plasma cells to antibody production by memory plasma cells. This is not unexpected, given that immune memory to many viruses and vaccines is stable over decades, if not for a lifetime.”

Read more …

Add to the list.

Ontario List Fluvoxamine As A Covid-19 Treatment To Consider (CTV)

Ontario has become the first province to list an inexpensive and well-known antidepressant as a treatment doctors can “consider” for patients with a mild COVID-19 infection in a bid to keep them out of hospital. In the science table listing on Wednesday, a panel indicated that the drug fluvoxamine can be considered and prescribed to patients with a mild case who are at risk of having more severe symptoms. Fluvoxamine is a selective serotonin reuptake inhibitor (SSRI) antidepressant that is typically used to treat depression and obsessive-compulsive disorders. “Right now, we’re in a really unprecedented wave of Omicron and we have just a staggering number of patients getting infected,” Dr. Menaka Pai, associate professor of medicine at McMaster University and co-chair of the Ontario COVID-19 Science Advisory Table, told CTV News.


“Our goal is to keep them safe, to keep them out of hospital and also to preserve our scarcest resource, which I would say is our hospital beds.” The drug costs a little more than a dollar a day and would be taken for 15 days, starting with a small dose. In comparison, the antivirals medicines from Pfizer and Merck cost nearly $1,000 dollars per patient. Studies have shown that the drug can cut hospital admissions due to COVID-19 by up to 30 per cent. “When you look at all that data together, it is very likely that fluvoxamine prevents hospitalization in patients with mild COVID-19,” Pai said. “So patients who are not yet on oxygen, and if our goal in this wave of the pandemic is to stop patients with COVID from ending up in those scarce hospital beds, then that I think is a very important finding, indeed.”

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“A fixture on the WHO’s list of 100 essential medicines all hospital systems are recommended to carry..”

A Myth is Born: How CDC, FDA, and Media Wove a Web of Ivermectin Lies (Resc.)

When a Texas cattleman, seventy-nine, died last September in New Mexico after contracting covid, his family never anticipated the worldwide headlines that would ensue. In a ballyhooed press conference, New Mexico Human Services Secretary Dr. David Scrase, the state’s top health chief, announced New Mexico’s first ivermectin “overdose,” soon adding a second fatality allegedly from “ivermectin toxicity.” Now, Scrase has acknowledged that his repeated, what he called “offhand,” assertions were groundless. Two deaths were not caused by ivermectin, a long-used generic drug that was emerging as a covid treatment. Instead, he said that the pair died because they “actually just delayed their care with covid.” That is a big difference.

Scrase backpedaled on December 1 in a little-noticed online press briefing and only after we pressed his agency to provide evidence for its claims of so-called “ivermectin deaths.” Officials had repeatedly said they were awaiting a toxicology report on the cattleman’s death. Yet we learned that the report was never even ordered or done, and, moreover, the man’s death was ruled by the state’s coroner as being from “natural” causes. Not a single media outlet reported Scrase’s admission, even as dozens, including the The Hill and The New York Times, had eagerly covered his original assertions about ivermectin, an anti-parasitic drug awarded the Nobel Prize in Medicine in 2015. “I don’t want more people to die,” read one early headline, quoting Scrase. “It’s the wrong medicine for something really serious,” Scrase said in the Times article.

Doctors, scientists, and toxicologists worldwide were puzzled by the assertions, because ivermectin is an extraordinarily safe, FDA-approved drug. A fixture on the WHO’s list of 100 essential medicines all hospital systems are recommended to carry, nearly four billion doses have been given in four decades. New Mexico became a key player in a broad pattern of governmental deception late last summer to portray ivermectin as dangerous, in tandem with three related developments. Research strongly supported the drug’s efficacy against covid; prescriptions were soaring; and public health officials were single-mindedly focused not on treatment but on vaccination.

We previously reported that the U.S. Food and Drug Administration’s tweeted warning last August against using ivermectin meant for livestock was prompted by incorrect—and unverified—information from Mississippi. Health officials there had posted an alert suggesting the state’s poison control center was deluged with hundreds of calls over ingestion of livestock ivermectin; in reality, we found, four reports were received. But, fueled by bits of contorted evidence like this, the anti-ivermectin train was unstoppable. We have now learned that, in the rush to bury a drug described as “astonishingly safe” and long used globally to quell animal and human parasites, FDA was not alone.

Read more …

CNN turns on Biden?!

‘Biden Seems Confused’: CNN Question President’s Cognitive Health (DM)

A CNN correspondent said Wednesday that Joe Biden ‘seemed confused’ in his ABC News interview earlier this week, when the president appeared to mix up COVID-19 at-home tests and antiviral pills. Biden, 79, spoke to ABC’s David Muir for 20 minutes in an interview that aired on Wednesday and defended his administration against criticism of its handling of the pandemic and readiness for the rapidly spreading Omicron variant, but also admitting that there were certain mistakes made. When asked about complaints that the lines to get tested for COVID-19 were excessive, with waits of over five hours in New York City as one example, Biden said that 500 million at-home tests had been ordered.

But several times he referred to the tests as ‘pills’ – potentially thinking of the Pfizer antiviral pills, which were federally approved on the same day. ‘Repeatedly throughout this interview – President Biden seems confused and was confusing the half a billion tests that they’ve ordered with a half a billion pills,’ said Jeff Zeleny, CNN’s chief national affairs correspondent. ‘Of course, pills were in the news today with the Pfizer approval of the anti-viral, so he corrected himself, but that was one thing that stuck out to me.’ Zeleny, appearing on Wolf Blitzer’s show on Wednesday afternoon, accused Biden of ‘really not accepting any responsibility’ for the lack of testing. Biden, asked whether the administration should not have seen Omicron coming and prepared accordingly, said ‘nobody saw it coming’.

Defiant, the president said they were doing the best they could. Zeleny said it was not enough. ‘Simply, this administration, and the president leading the charge here, really not accepting any responsibility at all for this lack of testing,’ Zeleny said. ‘We’ve seen these images across the country, long lines, just the inability to get tests. ‘And yes, Omicron came on very quickly here, but it has been almost a month since Thanksgiving where they knew this was coming. ‘So he said he wishes he could have acted faster, and then explains why he didn’t.’

Read more …

And Newsweek turns too…

Fauci et al Withheld Information on China’s Coronavirus Experiments (NW)

The NIH fought for more than a year to keep details about the EcoHealth grant under wraps. The 528 pages of proposals, conditions, emails, and progress reports revealed that EcoHealth had funded experiments at the WIV that were considerably riskier than the ones previously disclosed. The trouble began in May 2016, when EcoHealth informed the NIH that it wanted to conduct a series of new experiments during the third year of its five-year grant. One proposed producing “chimeras” made from one SARS-like virus and the spike proteins (which the virus uses to infiltrate animal cells) of others, and testing them in “humanized” mice, which had been genetically engineered to have human-like receptors in their lungs, making them better stand-ins for people. When such novel viruses are created, there is always a risk they will turn out to be dangerous pathogens in their own right.

Another risky experiment involved the MERS virus. Although MERS is lethal—it kills 35 percent of those who catch it—it’s not highly transmissible, which is partly why it has claimed fewer than 900 lives so far. EcoHealth wanted to graft the spikes of other related coronaviruses onto MERS to see how that changed its abilities. Both experiments seemed to cross the gain-of-function line. NIH program officers said as much, sending Daszak a letter asking him to explain why he thought they didn’t. In his reply, Daszak argued that because the new spikes being added to the chimeras were more distantly related to SARS and MERS than their original spikes, he didn’t anticipate any enhanced pathogenicity or infectiousness. That was a key distinction that arguably made them exempt from the NIH’s prohibition on gain-of-function experiments.

But, of course, one never knows; as a precaution, he offered that if any of the chimeric viruses began to grow 10 times better than the natural viruses, which would suggest enhanced fitness, EcoHealth would immediately stop all experiments, inform the NIH program officers, and together they’d figure out what to do next. The NIH accepted Daszak’s terms, inserting his suggestions into the grant conditions. Scientists at WIV conducted the experiments in 2018. To their surprise, the SARS-like chimeras quickly grew 10,000 times better than the natural virus, flourishing in the lab’s humanized mice and making them sicker than the original. They had the hallmarks of very dangerous pathogens.

WIV and EcoHealth did not stop the experiment as required. Nor did they let the NIH know what was going on. The results were buried in figure 35 of EcoHealth’s year-four progress report, delivered in April 2018. Did the NIH call Peter Daszak in to explain himself? It did not. There are no signs in the released documents that the NIH even noticed the alarming results. In fact, NIH signaled its enthusiasm for the project by granting EcoHealth a $7.5 million, five-year renewal in 2019. (The Trump administration suspended the grant in 2020, when EcoHealth’s relationship with the WIV came under scrutiny.)

Read more …

Because airports over the holidays were not chaotic enough yet..

US Airlines Cancel Hundreds Of Flights Scheduled For Friday (DM)

Hundreds of Christmas Eve flights have been canceled as the fast-spreading Omicron variant takes a toll on flight crews and other workers. Chicago-based United Airlines has canceled at least 120 flights for Friday, while Atlanta-based Delta said it has canceled about 90 and Alaska Airlines said it had canceled 17. United and Delta said they were working to contact passengers so they would not be stranded at airports. ‘The nationwide spike in Omicron cases this week has had a direct impact on our flight crews and the people who run our operation. As a result, we’ve unfortunately had to cancel some flights and are notifying impacted customers in advance of them coming to the airport,’ United said.


At least one of the airlines is making it clear that COVID is responsible for the cancellations. When accessing a cancelled flight on United’s website, the following message pops up: ‘Your flight is canceled due to an increase in Covid cases limiting crew availability. We’re sorry for disrupting your holiday plans and for the inconvenience.’ Delta said it has ‘exhausted all options and resources — including rerouting and substitutions of aircraft and crews to cover scheduled flying — before canceling around 90 flights for Friday.’ Delta cited potential inclement weather and the impact of the Omicron variant for the cancellations. Notably, American and Alaska had said they would comply with President Joe Biden’s COVID-19 vaccine mandate for government contractors, while Delta’s CEO had promised to fight the rule.

Read more …

“..We were put in a situation where we could not do otherwise..”

Putin Reveals Thinking Behind 2014 Moves In Crimea (RT)

Before the Maidan in 2014, Moscow was happy to work closely with all Ukrainian governments and had no plan to take any action in Crimea. However, this changed when a democratically elected leader was overthrown, the Russian president said on Thursday. Speaking to journalists at his annual end-of-year press conference at the Manezh Central Exhibition Hall in Moscow, Putin said he would have continued working closely with Ukrainian partners if there hadn’t been a “bloody coup d’etat,” in which people were “killed and burned.” The current tension between Russia and Ukraine began following the events of the 2014 Maidan, when violent street protests toppled a democratically elected government. Shortly after the uprising in Kiev, Crimea was reabsorbed into Russia following a referendum. The vast majority of the world considers the vote illegitimate and views the peninsula as illegally occupied by Moscow.


Before the Maidan, reabsorbing Crimea was not even on the cards, the Russian president said. “How could we say no to Sevastopol and Crimea, to the people who live there? How could we not take them under our protection, under our wing? Impossible. We were put in a situation where we could not do otherwise,” Putin said. The president also referred to a decision by the Soviet Union to create the Ukrainian Soviet Socialist Republic, which saw new borders created inside what was formerly the Russian Empire. According to Putin, those living in Crimea, as well as in the Donbass in eastern Ukraine, were not given a choice of which country they belonged to, and many of those locals wished to be Russian. “They created a country which never existed before,” he claimed, suggesting that today’s crises are ripple effects from that decision.

Read more …

 

 

 

 

 

 

 

 

 

 

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Dec 052021
 


Rembrandt van Rijn Study of the Head and Clasped Hands of a Young Man as Christ in Prayer 1655

 

1 In 2680 Young Men In Hong Kong Get Acute Myocarditis From Comirnaty (Malone)
120 Children Hospitalized In Vietnam Pfizer Vaccine Batch Suspended (Vne)
Twitter: Research On Potential Heart Risks Of Covid Vaccine ‘Unsafe’ (JTN)
WHO: Omicron in 38 Countries, No Deaths Reported (ET)
Do You Know Why There Isn’t An EUA For Fluvoxamine? (Kirsch)
‘Wall Of Secrecy’ In Pfizer Contracts As Company Accused Of Profiteering (G.)
Australian Children Aged 5 To 11 Set To Receive Pfizer Covid Vaccine
Molnupiravir Set For UK At-Home Trials (G.)
EU Chief Calls For Throwing Out Nuremberg Code (PM)
Hundreds Of NY Corrections Officers Put On Leave For Refusing Covid Jab (NYP)
Joe Biden Warns Vladimir Putin Not to Invade Ukraine (GR)
Obituary for Russiagate (Patrick Lawrence)

 

 

So we don’t blame them

 

 

Below is an article by Robert Malone about myocarditis in Hong Kong, which says 37.32 per 100,000 = 1 in 2680 young men are afflicted.

But Eric Topol says there are no cases among 5 million kids in the US. At the same ratio (and why shouldn’t there be), there should be 1,850. Irresponsible nonsense, Topol. 2nd hand car salesman.

Topol

 

 

“..Under conditions of terror most people will comply but some people will not, just as the lesson of the countries to which the Final Solution was proposed is that “it could happen” in most places but it did not happen everywhere.” – Hannah Arendt

 

 

They never found a cure for the “common” cold because the cold IS the cure.

 

 

“37.32 per 100,000 = 1 in 2680 young men who develop myocarditis/pericarditis within two weeks of their second vaccination..”

1 In 2680 Young Men In Hong Kong Get Acute Myocarditis From Comirnaty (Malone)

Strong data from a peer reviewed article in the journal of Clinical Infectious Disease shows that there is a significant increase in the risk of myocarditis/pericarditis following Comirnaty vaccination among Chinese male adolescents, especially after the second dose. Onset of myocarditis was a median of 2 days after vaccination. The clinically significant (acute and/or “mild”) myocarditis/pericarditis incidence rate came in at one out of every 2680 young males. The results conclude with : “Among male adolescents, the incidence after the first and second doses were 5.57 (95% CI 2.38-12.53) and 37.32 (95% CI 26.98-51.25) per 100,000 persons vaccinated.”

Analysis: 37.32 per 100,000 = 1 in 2680 young men who develop myocarditis/pericarditis within two weeks of their second vaccination (median time to disease: 2 days). This study was an analysis of hospital records of myocarditis/pericarditis, so did not include adolescents who may have developed the disease but did not seek medical attention. Many pediatric cardiologists including my colleague and friend Dr. Kirk Milhoan, MD, PhD (MD board certified in pediatric cardiology, PhD. in vascular inflammation) assert that there is no such thing as “mild” myocarditis in children. Myocarditis causes heart damage. Heart damage is for life – the heart does not heal by replacing damaged cells. It scars. Scars in the heart can lead to changes in electrical conduction in heart muscle, which in turn can result in “sudden death” due to changes in heart beat regularity and muscular contraction of the heart. These events may happen at any time, particularly when the heart is stressed in some way.

Results (from the abstract) Between 14 June 2021 and 4 September 2021, 33 Chinese adolescents who developed acute myocarditis/pericarditis following Comirnaty vaccination were identified. 29 (87.88%) were males and 4 (12.12%) were females, with a median age of 15.25 years. 27 (81.82%) and 6 (18.18%) cases developed acute myocarditis/pericarditis after receiving the second and first dose, respectively. All cases are mild and required only conservative management. The overall incidence of acute myocarditis/pericarditis was 18.52 (95% Confidence Interval [CI], 11.67-29.01) per 100,000 persons vaccinated. The incidence after the first and second doses were 3.37 (95%CI 1.12-9.51) and 21.22 (95%CI 13.78-32.28 per 100,000 persons vaccinated, respectively. Among male adolescents, the incidence after the first and second doses were 5.57 (95% CI 2.38-12.53) and 37.32 (95% CI 26.98-51.25) per 100,000 persons vaccinated.

Conclusion from the Abstract “There is a significant increase in the risk of acute myocarditis/pericarditis following Comirnaty vaccination among Chinese male adolescents, especially after the second dose.”

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Just a batch? Let’s see the follow-up.

120 Children Hospitalized In Vietnam Pfizer Vaccine Batch Suspended (Vne)

Thanh Hoa has suspended the use of a Pfizer Covid-19 vaccine batch after over 120 students were hospitalized following their inoculation. Since November 30, the central province has been vaccinating children aged 15-17 with the Pfizer Covid-19 vaccine. However, over 120 of the children were admitted to hospitals after exhibiting symptoms like nausea, high fever or breathing difficulties, the provincial Center for Disease Control (CDC) said Thursday. Of these, 17 had severe reactions, but their health has stabilized and they continue to be monitored at the hospital, the center said. The cause of their symptoms has yet to be confirmed by Thanh Hoa authorities.

Thanh Hoa CDC director Luong Ngoc Truong said the province has stopped using the current vaccine batch. “We still have other batches, also Pfizer vaccines, so we will continue vaccinating the children,” he said. The suspended batch would be put into storage and could be used later for other groups like adults, Truong added. Vu Van Chinh, director of the Ha Trung District General Hospital, said side-effects following vaccination was normal, but are more likely to happen in children than adults. “Those who have reactions or faint need to be separated so no chain reaction occurs,” said Chinh.

The Thanh Hoa CDC has distributed around 117,000 Covid-19 vaccine doses to 27 districts and towns. Over 56,700 doses have been administered. Over the past week, three children have died following their vaccination with the Pfizer Covid-19 vaccine in Bac Giang, Hanoi and Binh Phuoc. The cause of death has been determined as “overreaction to the vaccine.” Last week, four workers in Thanh Hoa’s Kim Viet Shoe factory died following their Vero Cell Covid-19 vaccination, also due to “overreaction.”

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It’s not the vaccine that’s unsafe, it’s the research.

Twitter: Research On Potential Heart Risks Of Covid Vaccine ‘Unsafe’ (JTN)

Twitter this week ignited controversy when it slapped an “unsafe” label on a research abstract regarding potential heart effects arising from the use of COVID-19 mRNA vaccines. The abstract in question, “Mrna COVID Vaccines Dramatically Increase Endothelial Inflammatory Markers and ACS Risk as Measured by the PULS Cardiac Test: a Warning,” claims that research suggests those vaccines “dramatically increase inflammation on the endothelium and T cell infiltration of cardiac muscle” and that the purported side effects “may account for the observations of increased thrombosis, cardiomyopathy, and other vascular events following vaccination.” The abstract, published in the American Heart Association-affiliated journal Circulation, drew an “expression of concern” from the AHA’s Committee on Scientific Sessions Program.


That statement claimed that, within the article, “there are several typographical errors, there is no data in the abstract regarding myocardial T-cell infiltration, there are no statistical analyses for significance provided, and the author is not clear that only anecdotal data was used.” Twitter subsequently applied the “unsafe” warning to the original article, with users who click through to the abstract being told that the research “could” constitute, among other potential categories, “violent or misleading content that could lead to real-world harm.” The original abstract was published by controversial American cardiac surgeon Steven Gundry, who has been criticized for his theories on the link between heart inflammation and lectins.

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Some people must be disappointed. They’ll find a way.

WHO: Omicron in 38 Countries, No Deaths Reported (ET)

The World Health Organization (WHO) on Friday said the COVID-19 omicron variant is now in 38 countries, up from 23 two days ago, suggesting that the variant may be more contagious than Delta. During a news conference, WHO official Maria Van Kerkhove said the U.N. health body has seen “an increasing growth rate,” and “we see increasing numbers of Omicron being detected.” No deaths have been reported so far in connection to the COVID-19 strain, another WHO spokesperson told reporters Friday. “There is a suggestion that there is increased transmissibility, what we need to understand is if it’s more or less transmissible compared to Delta,” Van Kerkhove said. The Delta variant is the dominant strain throughout the world, she said.

In the United States, at least six U.S. states have confirmed Omicron cases so far, including a fully vaccinated male who traveled from an anime convention in New York City to Minnesota this week, according to health officials, who said the individual had mild symptoms and recovered. The first American case was detected in California’s San Francisco Bay Area. A previous update from WHO said Omicron has numerous mutations to its spike protein, which is what it uses to bind to human cells, which may lead to higher transmission rates. It’s not yet clear, however, officials have cautioned. But whether the new strain causes more severe disease or not is unclear, Van Kerkhove said. Early reports from South Africa and Israel suggest many patients experience mild symptoms.

Van Kerkhove said that the first Omicron cases were based on a cluster of college students, noting that younger people tend to experience milder symptoms than older people. A top South African doctor this week told news outlets that the symptoms were unusual but “extremely mild.” “There was initial reports that it tended to be more mild, but it’s really too soon,” Van Kerkhove said. “Everybody who is infected with SARS-CoV-2 regardless of what variant will always start out with a mild disease. And so maybe it will stop there with mild, some people are asymptomatic of course, but it may stop with mild disease or it may take some time.”

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“Basically, the system is set up so that only proprietary drugs that can kill you are approved.”

Do You Know Why There Isn’t An EUA For Fluvoxamine? (Kirsch)

The reason is simple. We tried. And after 6 weeks of waiting, we were told that to get an EUA for a repurposed drug, you have to partner with a drug company in the EUA application. Because no drug company will partner with us, even if we pay all the filing costs, there won’t be an EUA. Ever. So most doctors will never prescribe it for COVID, even thought it works better than anything else. And the NIH won’t do anything with fluvoxamine either like add it to their guidelines. It will never be upgraded on the NIH COVID treatment guidelines. It is currently sitting at “NEUTRAL” after two trials where it had a 100% risk reduction in both trials without any downside risk. In short, if deployed it would likely save a lot of lives and there is no risk of deployment since the risks of the drug are well known.

It’s a very safe drug when properly prescribed. I took it myself and I couldn’t tell I was on it the side-effects were so negligible. When the fluvoxamine Phase 3 study published in Lancet showed the drug worked better than any other drug (including the new antiviral pills from Merck and Pfizer), the NIH simply ignored the study. They didn’t even mention it. Even 60 Minutes which did a story on fluvoxamine didn’t mention the Phase 3 study proved it worked when the study came out (normally, they’d do this at the end of a show to let their audience know they got it right). Fluvoxamine provides a 12-fold reduction in death if you started the drug early, but the NIH basically said “Ho hum. Only 12X reduction in death? That’s better than anything including the vaccines (which according to the Pfizer 6 month Phase 3 study was only a 2X reduction in mortality).

So not even worth mentioning in the guidelines. It would save too many lives. Best to ignore it. And if we ignore it, no doctor in America will dare to prescribe it. So the vaccine will be the only option just like we planned.” Cliff Lane, who heads the guidelines committee, reports to Fauci. Cliff simply isn’t going to allow the NIH recommendation to be modified no matter what the science says. This is not about saving lives. It never was. When the key opinion leader (KOL) panel of NIH, CDC, FDA and academia experts recommended fluvoxamine be used back in January 2021, the NIH ignored that too. Jeffrey Klausner, who convened the panel, wrote a great op-ed about it in the Washington Post right after the meeting so everyone would know. Doctors ignored it.

Klausner shopped the KOL meeting notes to 10 journals, all of whom refused to publish it. Truly stunning! Life saving drug and nobody would publish the recommendation of an expert panel to use it. Wow. When the KOL meeting notes were finally published in the peer-reviewed medical literature on December 1, 2021, only 12 months after the meeting, the NIH again did absolutely nothing, ignoring the advice of these key experts, even though now they have more data from the Together trial showing it works. Basically, the system is set up so that only proprietary drugs that can kill you are approved.

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The Guardian turns on Pfizer?

‘Wall Of Secrecy’ In Pfizer Contracts As Company Accused Of Profiteering (G.)

Ministers have agreed a secrecy clause in any dispute with the drugs manufacturer Pfizer over Britain’s Covid vaccine supply. Large portions of the government’s contracts with the company over the supply of 189m vaccine doses have been redacted and any arbitration proceedings will be kept secret. The revelation comes as Pfizer is accused by a former senior US health official of “war profiteering’’ during the pandemic. In a Channel 4 Dispatches investigation to be broadcast this week, Tom Frieden, who was director of the US Centers for Disease Control and Prevention under Barack Obama, said: “If you’re just focusing on maximising your profits and you’re a vaccine manufacturer … you are war profiteering.”

Zain Rizvi, research director at Public Citizen, a US consumer advocacy organisation which has examined Pfizer’s global vaccine contracts, said: “There is a wall of secrecy surrounding these contracts and it’s unacceptable, particularly in a public health crisis.” Rizvi said the UK needed to explain why it had agreed to secret arbitration proceedings. He said: “It’s the only high-income country we have seen that has agreed to this provision. It allows pharmaceutical companies to bypass domestic legal processes. “The UK government has allowed the drug firms to call the shots. How did we end up in a situation where a handful of drug firms were able to exert so much control over the most powerful governments in the world? It points to a broken system.”

Pfizer has won plaudits for its vaccine delivery programme, but the US multinational faces growing scrutiny over the scale of its profits and the proportion of doses it has delivered to low-income countries. While AstraZeneca agreed to sell its vaccine at cost during the pandemic, Pfizer wanted to secure its profits. The Pfizer/BioNTech vaccine, which now has the brand name Comirnaty, will be one of the most lucrative drugs in pharmaceutical history. The Channel 4 investigation reveals analysis by one biological engineering expert claiming the Pfizer vaccine costs just 76p to manufacture for each shot. It is reportedly being sold for £22 a dose to the UK government.

The estimated manufacturing costs do not include research, distribution and other costs, but Pfizer says its profit margin as a percentage before tax are in the “high-20s”. Pfizer expects to deliver 2.3bn vaccines this year with predicted revenues of $36bn (£26.3bn).

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Big trial. Population wide.

Australian Children Aged 5 To 11 Set To Receive Pfizer Covid Vaccine

Australian children aged five to 11 could receive the Pfizer vaccine against Covid as soon as 10 January, following provisional approval by the country’s drugs regulator. The Therapeutic Goods Administration (TGA) green light, announced by the federal health minister, Greg Hunt, on Sunday will likely be followed by an independent recommendation from the Australian Technical Advisory Group on Immunisation (Atagi) to use the vaccine in that age group. Hunt told reporters the provisional approval was “about keeping our kids safe, keeping our families safe, keeping all Australians safe”. “From 10 January, Australian children will have access to Pfizer vaccines, and it is recommended for children right across Australia,” he said in Melbourne.

Hunt said the TGA was also considering children’s doses of Moderna, the other mRNA vaccine, and will form a view on that “in the coming weeks”. The head of the TGA, Prof John Skerritt, said the Pfizer vaccine had been “extensively clinically tested” including a trial of 2,500 children aged five to 11. “The response of the body, the immune response, was identical to that in young adults,” he said. “There were … no safety problems identified in those trials. The children had some of the same things that adults get – tiredness, sore arms, headache and so forth – but these tended to be brief and fairly short-lived.” Skerritt said the children’s Pfizer was the “same vaccine” but “formulated differently for children” – using one-third of an adult dose.

[..] Hunt said 92.8% of Australians aged 16 and over have now had a first dose of a Covid-19 vaccine and 88% were double-dosed. Since vaccinations were opened to the 12 to 15 age group in September, more than three quarters (76.7%) in that cohort have received a first dose while two-thirds (67.8%) have had two doses.

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We know Molnupiravir doesn’t work. But:

“The UK has proven itself to be a world leader in identifying and rolling out effective treatments for Covid-19..”

Yeah, they have humor..

Molnupiravir Set For UK At-Home Trials (G.)

The first at-home treatment for Covid-19 could reportedly be offered to UK patients before Christmas as an attempt to protect the most vulnerable from the Omicron variant. The Sunday Telegraph reported that Sajid Javid is set to launch a national pilot of the Molnupiravir antiviral pill, marketed as Lagevrio. The newspaper said that under the plans, the NHS was expected to deliver courses of the tablet to clinically vulnerable and immunosuppressed patients within as little as 48 hours of them testing positive for Covid. It said hospitals and GPs had been told a series of Covid medicines delivery units were being established to ensure the treatment gets to patients as quickly as possible once it is confirmed they have the virus. Last month, the UK became the first country in the world to license its use – a move described as a “gamechanger” by Javid, the health secretary.


But just over a week ago, England’s chief medical officer, Prof Chris Whitty, warned its use may have to be reconsidered in the light of the emergence of Omicron. “I think we probably need to do a rethink of it just to make sure with the new variant, we’re targeting in the right direction.” A Department of Health and Social Care spokesman said: “The UK has proven itself to be a world leader in identifying and rolling out effective treatments for Covid-19, including through government-backed national trials. “The government’s antivirals taskforce was launched to identify treatments for UK patients who have been exposed to Covid-19 to take at home, stopping the infection spreading and speeding up recovery time. “There are a number of exciting opportunities in the pipeline and we will provide further details in due course.”

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This warrants a lot more scrutiny.

EU Chief Calls For Throwing Out Nuremberg Code (PM)

Ursula Van Der Leyen, the head of the EU commission, told the press on Wednesday that she is in favour of scrapping the long-standing Nuremburg Code and forcing people to get vaccinated against COVID. In an interview she gave to the BBC, the EU chief said that it was “understandable and appropriate” to consider vaccine mandates, especially due to the new Omicron variant of COVID 19, which has been now detected in 12 different member nations of the EU. “How we can encourage and potentially think about mandatory vaccination within the European Union? This needs discussion. This needs a common approach, but it is a discussion that I think has to be led,” commented Van Der Leyen to the BBC.


The WHO, however, has strongly encouraged countries not to enact travel bans because of Omicron, and further iterated that early data points to the fact that most Omicron cases are not severe. Most of the world’s governments are not paying attention to the WHO’s guidelines on this occasion, however. The Nuremberg Code was enacted in 1947, immediately after the Second World War to prevent many of the egregious human rights abuses enacted by the Nazis and the Imperial Japanese during the war. Especially were at issue the performance of medical procedures on subjects without their consent. These procedures, often performed under the command of people such as Dr. Josef Mengele or Hideki Tojo, often were akin to the worst kinds of torture. Since then, full and proactive ongoing consent has been required.

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It’s all about safety.

Hundreds Of NY Corrections Officers Put On Leave For Refusing Covid Jab (NYP)

More than 500 officers with the already depleted city Department of Corrections are still refusing to get vaccinated against COVID-19 and remain on unpaid leave. New data released by the city shows 17% of DOC uniform officers had yet to receive at least one jab as of Thursday night – two days after a deadline imposed by Mayor Bill de Blasio kicked in requiring proof of inoculation for them to continue working. Most city workers had until Oct. 29 to get vaccinated or be placed on unpaid leave until they provide proof of vaccination. However, de Blasio gave uniformed correction officers extra time — until Dec. 1 — to receive their first jab, because of the ongoing staffing shortage at the troubled Rikers Island jail complex.


Although the DOC’s 83% vaccination rate is the lowest of any city agency, the DOC has seen its rate rise significantly from 46% when de Blasio’s October mandate went into effect, and 77% when the correction officer deadline recently kicked in. Another 9% of DOC uniformed staff who have applied for medical or religious exemptions are continuing to report to work as the city reviews their cases, meaning 92% of the uniformed workforce is active. Councilman Keith Powers (D-Manhattan), who chairs the criminal justice committee that oversees city jails, said the mandates are working, adding “we still have work to do, but the current numbers present progress.” The mayor gave the DOC permission to assign 12-hour shifts and “any other measures necessary to address the current staffing shortage” earlier this week as the agency prepared for an employee shortage.

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Russia invading Ukraine is a story the US made up. So it can warn against it.

Joe Biden Warns Vladimir Putin Not to Invade Ukraine (GR)

President Joe Biden said on Friday that he and his administration have plans to make it “very, very difficult” for Russian President Vladimir Putin to invade Ukraine. Biden and his team are creating a new set of initiatives to check Russia and make sure Ukraine is protected. But Biden made sure to calmly issue a warning to Putin before any of said initiatives become necessary. The U.S. President is primarily concerned with an increased presence of Russian troops at the Ukrainian border. The Kremlin has also boasted war-ready rhetoric in its recent language. “What I am doing is putting together what I believe will be the most comprehensive and meaningful set of initiatives to make it very, very difficult for Mr. Putin to go ahead and do what people are worried he may do,” Biden told the press.

There are indications that the tensions are high enough that a meeting between the White House and the Kremlin may be held as soon as next week. Putin’s foreign affairs adviser Yuri Ushakov told the press that the Kremlin had been organizing a call between the two leaders in the next coming days. Will Biden has made sure not to name any specific consequences he is considering, Russian Foreign Minister Sergey Lavrov said that he believes that Biden will put pressure on Russia with new sanctions. Lavrov spoke with U.S. Secretary of State Antony Blinken in Stockholm, Sweden on Thursday, where Blinken said that the U.S. would “have to respond” if Russia acted on Ukraine:

“We don’t know President Putin’s intent. We don’t know if he’s made a decision to take renewed, aggressive action against Ukraine, but what we do know is that he’s putting in place the capacity to do so and to do so on short, on short notice,” Blinken said in a statement to Euronews following the meeting. But Lavrov seemed unshaken by Blinken’s remark and Biden’s warning, saying that “If the new ‘sanctions from hell’ come, we will respond. We can’t fail to respond.”

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Anybody can write one of these now. But how, looking at the fall-out, can you leave out the Covid hysteria? It’s lessons learned from Russiagate, on steroids.

Obituary for Russiagate (Patrick Lawrence)

There is, of course, the more dangerous world Russiagate has done so much to create. In the culture of unreason, the Deep State has a discouraging record of success in gaining wide public support for any aggressive campaign against any nation or people it wishes to act against. In this dimension, Russiagate has destroyed the Democrats as a party willing to stand against the imperial project in its late phase. A war with China over the Taiwan question is now spoken of as a logical possibility. Washington is now raising the temperature on the Ukraine–Russia border, just as it did when it cultivated the 2014 coup in Kiev, and this is put across as a Democratic administration’s sound policy. Rampant Russophobia is a direct consequence of the Russiagate ruse, Sinophobia its uglier sibling — uglier for its racist subtext.

We have active subversion operations in Nicaragua, Venezuela, Cuba and Peru, all progressive states in the true meaning of this term, and Democrats of all stripes — including “progressives” with the necessary quotation marks — cheer on every one of them. We cannot view this as distinct from the elevation of institutions dedicated to campaigns of covert subterfuge — chiefly but not only the C.I.A. — to wholly inappropriate positions of respect. The damage Russiagate has done to the press … let me rephrase this. The damage the press has inflicted upon itself in the cause of Russiagate is so extensive it is hard to calculate with any precision. We watch now as their credibility collapses in real time. Those running the mainstream newspapers and networks seem to understand this, as they rush to protect what remains of their reputations with rearguard actions to obscure their grossly irresponsible conduct.

The long list of those who caved to the Russiagate orthodoxy includes some stunning names. Among publications that should have known better we find Mother Jones, The Nation, The Intercept, and Democracy Now! Was it conformity, pressure from donors or Democratic Party ventriloquists, or some combination of ideology, ignorance and inexperience that caused them to flip? The Atlantic, The New Yorker, the major dailies, the networks — they have all sustained one or another degree of discredit, left either to craven rewrites in their archives, denial in the Corn–Frum mode, or silence. None will do: They will never regain lost ground without first acknowledging what they have done, and this appears out of the question.

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Melbourne

 

 

Vienna

 

 


This photo is the most detailed model of a human cell to date, obtained using X-ray, NMR, and cryo-electron microscopy data sets

 

 

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