More good news on vaccine, folks. First, you may be required to take only one Covid-19 shot per year, and if all goes well you will not even have to do that. You will be able to drink or even inhale your vaccine. No more painful injections, just a quick slurp or a snort and the job’s a good ’un. That’s you safe from the deadly virus for another year.
We could even make it fun. Why not hold Covid-19 vaccine parties? A selection of flavours in shot glasses (they don’t call them shot glasses for no reason) or add your vaccine to a vape and puff away until your immune system is primed.
I glean all this garbage from Global Health Now, the daily newsletter from the Johns Hopkins Bloomberg School of Public Health. The first story concerns how the Food and Drug Administration (FDA) in the United States is considering ‘simplifying the Covid vaccination schedule, allowing most people to get the currently available booster, regardless of how many doses they had received before that’. This means that if you are boosted up to the eyeballs or have never had one before and suddenly made the incomprehensible decision to start now, then Bob’s your uncle; roll up your sleeves.
Please note that nothing has changed; there is no new vaccine and no new threat. The FDA is just making an arbitrary decision to change the schedule. Clearly the aim is to get more people to accept the vaccination. But it is also clear that they are making this stuff up as they go along. They have no further evidence that the vaccines will work any better this way.
The information that is available to them is the abundant and accumulating evidence of vaccine harms which, incredibly, the Medicines and Healthcare products Regulatory Agency (MRHA) in the United Kingdom admits can be serious while insisting that the vaccines are safe. If truth is the first casualty of war – it certainly died early in the Covid-19 madness – logic is not far behind it. The MRHA is willing to trade off serious vaccine side effects against minimal protection from a virus which is virtually harmless to the vast majority of people. Perhaps the FDA is trying to reduce the number of boosters it says people will need in the hope that vaccine injuries will go away. Alternatively, it may be keen to accelerate the rollout before the general population wakes up to the fact that they are being conned, if they are lucky, and killed if they are not.
The potential for a drinkable/snortable/inhalable vaccine comes courtesy of US Speciality Formulations, a company which has produced the QYNDR vaccine. If QYNDR is a bit of a consonant-rich mouthful, then be informed that the official pronunciation if ‘KINDER’. And the advent of QYNDR is closer than you think. Phase 1 trials have already been completed in New Zealand (where else?) and all that is required is more funding to proceed with further trials. Apparently, it is very difficult to formulate a vaccine that survives the vicissitudes of the digestive tract.
And why do we need these vaccines? Well, according to US Speciality Formulations: ‘Covid-19 is still here and deadly.’ Also, I imagine that the inventors and investors envisage that this will make them shedloads of money. It clearly pays to perpetuate the Covid-19 narrative and to pepper it with as much panic as possible.
At some point in the panic-demic, the vaccine rollout became a juggernaut. Large and hard to stop. With the widespread and obvious extent to which people are gullible, government and drug manufacturers are willing to lie, health professionals are willing to stay silent and there are bucks to be made, it is unlikely that the juggernaut will be halted any time soon.
Who knows what’s next? Perhaps they will develop a vaccine that one can stick up one’s bottom. Whether or not they do, I strongly advise them that is what they can do with the present products.
February 4, 2023
Posted by aletho |
Deception, Science and Pseudo-Science | Covid-19, COVID-19 Vaccine, FDA, UK, United States |
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We genuinely urge doctors involved with medical regulation not to go down with the sinking ship of authoritarian censorship and suppression of intellectual freedom. Not only is this behaviour historically illiterate and intellectually feeble, it is putting the safety of patients at risk, causing hazards to public health, runs counter to our community standards of a liberal democracy, and sits in conflict with the societal benefits of intellectual freedom that have recently been stated by the High Court of Australia.
When has there been a society that prospers because people are cancelled, removed, or ‘disappeared’ from their vital work because they dared to disagree with the ‘regime’s unquestionable truth?’ Do our modern medical authoritarians want to be looked back on with the same pathetic disdain with which we judge similar historical despots?
In this article we present two rays of hope in the context that the tide is changing. Firstly, for those doctors who genuinely want to have an open expression of ideas, there is a High Court precedent about the benefits to society of intellectual freedom where professional views asserted in the context of intellectual freedom can be expressed forcefully even if they cause offence, embarrassment, or lack of trust.
Secondly, for those doctors who continue to persecute other doctors for participating in the act of intellectual freedom, accumulated medical, ethical and legal information – we believe this warrants consideration that those doctors involved with AHPRA and the Medical Board of Australia themselves have their licenses suspended as they potentially pose a danger to the public’s health, in our opinion.
Go forth and be confident in the concept of intellectual freedom
Recent controversy has surrounded the sanctioning, by regulatory authorities, of doctors for publicly expressing views on elements of the Covid pandemic. Doctors have been punished because they sought to bring critical (if not ideologically uncomfortable) medical information to the public’s awareness.
This controversy is fundamentally about the limits of intellectual freedom doctors have within the constraints of general, and often highly subjective, Codes of Conduct that doctors must adhere to. In this context, a recent unanimous High Court of Australia judgment gives an important window into how the Court considers what the boundaries of intellectual freedom are and how the Court considers attempts by authorities to curtail such freedom under the guise of ‘conduct.’ (Find the example in detail at the end of the article.)
Although the case of Ridd v James Cook University (JCU) involved specific clauses within an Enterprise Bargaining Agreement, the High Court included valuable commentary on the societal importance of intellectual freedom from an instrumental, ethical, and historical perspective. This provides a useful context for academic freedom in general. Inherent in the developed concept of intellectual freedom is the ability to dissent against the establishment narrative. It is one of the modern marvels of living in a liberal democracy and brings tremendous benefit to society, as affirmed by the High Court:
‘Once developed, justification for intellectual freedom is instrumental. The instrumental justification is the search for truth in the contested marketplace of ideas, the social importance of which Frankfurter J spoke powerfully about.’
The Court further affirmed that:
‘Another justification is ethical rather than instrumental. Intellectual freedom plays “an important ethical role, not just in the lives of the few people it protects, but in the life of the community more generally” to ensure the primacy of individual conviction: “not to profess what one believes to be false” and “a duty to speak out for what one believes to be true.”’
Although doctors do not have a specific clause guaranteeing them the right to intellectual freedom, the High Court’s discussion of the societal benefits makes it difficult to argue that doctors should be punished for participation in the act of intellectual freedom.
There have been suggestions that the sanctioning of doctors has not necessarily been for the content of their views but how they have expressed them; invoking concepts such as incivility, rudeness, bullying, and harassment.
The Court explicitly addressed this issue in Ridd v JCU and was forthright in the view that intellectual freedom is not always pretty and wrapped in civility; curtailment on these grounds necessarily involves an assault on the fundamental phenomenon of intellectual freedom itself:
‘The instrumental and ethical foundations for the developed concept of intellectual freedom are powerful reasons why it has rarely been restricted by any asserted “right” of others to respect or courtesy … however desirable courtesy and respect might be, the purpose of intellectual freedom must permit of expression that departs from those civil norms.’
Furthermore, the Court reinforced the concept that there is no right against embarrassment or against lack of trust resulting from someone else’s assertions made in the course of intellectual freedom.
The Court quotes Dworkin:
‘The idea that people have that right [to protection from speech that might reasonably be thought to embarrass or lower others’ esteem for them or their own self-respect] is absurd. Of course, it would be good if everyone liked and respected everyone else who merited that response. But we cannot recognise a right to respect, or a right to be free from the effects of speech that makes respect less likely, without wholly subverting the central ideals of the culture of independence and denying the ethical individualism that culture protects.’
For the public’s safety it’s time to cancel the cancellers
It is absolutely frightening that major medico-legal organisations have issued advice to doctors to be wary about participating in intellectual freedom and that even reporting on evidence-based scientific data might put them in peril of being professionally ‘disappeared’ if that data doesn’t conform with the government’s ‘messaging.’ Is that what the community at large expects?
Sure, the regime may allow some new information if it is from a regime-approved source and disseminated in a way that the regime approves. But that defeats the whole purpose of intellectual freedom and merely perpetuates the formation of insular establishment echo chambers. A previous article showed the mass lethality of that group-think and establishment thinking during the first world war until dissident thinkers like General Sir John Monash came along.
But what about supposedly ‘bad ideas?’
Firstly, if those ideas are plausible, then as the High Court says, the truth is found in the ‘contested marketplace of ideas.’ If they are really bad ideas, then the sunlight of rigorous intellectual critique is the best disinfectant. Does driving a bad idea underground really make people think, ‘Oh well, the government told me it’s wrong, so it must be?’
Dr Li Wenliang was credited as one of the first doctors in Wuhan to sound the alarm about Covid on social media.
‘In early January (2020), he was called in by both medical officials and the police, and forced to sign a statement denouncing his warning as an unfounded and illegal rumor.’ [New York Times] Sound familiar?
Dr Li was among ‘eight people reprimanded by security officers for “spreading rumours.” [Int J Infect Dis.] Sadly Dr Li died of Covid. But during his illness he advocated that “I think a healthy society should not have just one voice.”’ [New York Times]
And it is accepted that chilling the expression of ideas (by making people scared to speak out) is just as detrimental as the specific banning of ideas.
Scholars of history, the Australian public at large, Dr Li and the High Court of Australia, understand the importance of the developed concept of intellectual freedom.
In this context, intellectual freedom is so important to knowledge advancement through, as the High Court ruled regarding ‘the contested marketplace of ideas,’ that banning intellectual freedom (unilaterally removing that contested marketplace) poses a serious risk to public health. Therefore, should doctors associated with AHPRA or the Medical Board of Australia who have participated at all in the dangerous repression of intellectual freedom have their licences to practice medicine immediately suspended while a thorough investigation is undertaken into their fitness to practice?
What builds trust in an institution? Intellectual freedom through open scientific discourse or enforced adherence to the regime’s singular ‘truth’ under the threat of professional excommunication?
Public health is still dependent on individuals receiving informed consent about treatments, consent being specific to the individual patient.
This introduces the last issue where transparency should be favoured over repression. If any information comes to light that would materially alter someone’s decision to give/not give consent (and that information was suppressed as a result of the chilling effect on intellectual freedom by AHPRA/Medical Board’s censorship), then AHPRA and the Medical Board should be open to both civil and criminal liability for any harm caused due to the silence they fashioned.
Statements by the High Court of Australia in Ridd v James Cook University
One developed justification for intellectual freedom is instrumental. The instrumental justification is the search for truth in the contested marketplace of ideas, the social importance of which Justice Felix Frankfurter spoke powerfully about in Sweezy v New Hampshire. Another justification is ethical rather than instrumental. Intellectual freedom plays ‘an important ethical role not just in the lives of the few people it protects, but in the life of the community more generally’ to ensure the primacy of individual conviction: ‘Not to profess what one believes to be false’ and ‘a duty to speak out for what one believes to be true.’
Whilst different views might reasonably be taken about some additional restrictions upon intellectual freedom, the instrumental and ethical foundations for the developed concept of intellectual freedom are powerful reasons why it has rarely been restricted by any asserted ‘right’ of others to respect or courtesy. It is not necessary to go as far as Said’s assertion that ‘the whole point [of an intellectual] is to be embarrassing, contrary, even unpleasant’ to conclude that, however desirable courtesy and respect might be, the purpose of intellectual freedom must permit of expression that departs from those civil norms.
JCU’s submission depends upon drawing a distinction between what is said and how it is said. But such a distinction may not exist. The content of what is said often depends upon how it is said. This is particularly so when impugned speech concerns the expression of an opinion. The content of speech that expresses an opinion will often be inseparable from the strength of conviction with which the opinion is held, which is tied to the manner of expression. The message conveyed by a statement, expressed tentatively ‘It may be that it was an error for Professor Jones to claim that the earth is flat’ expresses a proposition only of possibility. It cannot be divorced from the tentative manner in which it was expressed. By contrast, ‘no reasonable person could ever claim that the earth is flat’ expresses a proposition of certainty, all the more so if it is expressed in an emphatic manner.
That interpretation aligns with the long-standing core meaning of intellectual freedom. Whilst a prohibition upon disrespectful and discourteous conduct in intellectual expression might be a ‘convenient plan for having peace in the intellectual world,’ the ‘price paid for this sort of intellectual pacification, is the sacrifice of the entire moral courage of the human mind.’ The 2016 Censure given to Dr Ridd was, therefore, not justified.
Michael Keane is adjunct associate professor, Swinburne University, Adjunct senior lecturer, Monash University and a specialist anaesthetist.
February 4, 2023
Posted by aletho |
Civil Liberties, Full Spectrum Dominance, Science and Pseudo-Science, Timeless or most popular | Australia, Human rights |
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Meta’s Instagram and Facebook platforms have removed a video by Project Veritas showing a journalist confronting YouTube’s Vice President of Trust and Safety Matt Halprin about the censorship of a video showing a Pfizer executive talking about mutating viruses.
Both platforms claimed that the video was in violation of Community Standards, specifically the policy prohibiting “content that could lead to identity theft or put someone at risk of physical or financial harm.”
In the video that was removed by both platforms, Project Veritas’ journalist Christian Hartsock asked Halprin why he banned a video showing Pfizer’s Director of Research and Development, Strategic Operations Jordan Trishton Walker talking about mutating viruses.
“How much is Pfizer paying you to run cover for them?” said Hartsock. “Is YouTube brought to us by Pfizer?”
On January 25, Project Veritas posted a video of Walker talking about the company mutating COVID-19 virus. Walker later said he made it up.
“Well, one of the things we’re exploring is, why don’t we just mutate it ourselves so we could preemptively develop new vaccines, right?” said Walker.
“If we’re gonna do that, though, there’s a risk of, as you can imagine, no one wants to be having a pharma company mutating fucking viruses.”
YouTube banned the video.
February 4, 2023
Posted by aletho |
Full Spectrum Dominance | Covid-19, COVID-19 Vaccine, Facebook, Instagram, YouTube |
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Israeli occupation settlers and forces have committed 3,532 violations against Palestinians in the occupied West Bank and Jerusalem in January, the Palestine National Information Centre revealed.
The Information Centre disclosed in a report that January was the bloodiest month in the occupied West Bank since 2015, citing the Israeli killings of 35 Palestinians, including eight children and a 61-year-old woman – with 20 killed in Jenin alone.
In addition, the report also pointed out that the Israeli occupation settlers and forces wounded 342 Palestinians.
According to the Information Centre, the occupation settlers committed 17 settlement activities, including stealing land, razing farms, paving new settlement roads and approving new settlement units, in addition to 319 aggressions.
Meanwhile, the occupation forces and settlers demolished 290 commercial and agricultural facilities and confiscated 40 others.
The Information Centre also documented the Israeli demolition of 40 Palestinian homes and issued 154 demolition notices.
It documented 29 aggressions on holy sites, road closures in 38 areas and 511 temporary and permanent Israeli military checkpoints across the occupied West Bank and Jerusalem.
February 4, 2023
Posted by aletho |
Ethnic Cleansing, Racism, Zionism | Israel, Palestine, West Bank, Zionism |
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US Attorney General Merrick Garland announced on Friday the first transfer of assets, confiscated as part of anti-Russia sanctions, to Ukraine to pay for the country’s reconstruction.
The measure affects $5.4 million expropriated from Russian businessman Konstantin Malofeyev on charges of sanctions evasion, according to the top official.
“With my authorization today, forfeited funds will next be transferred to the State Department to support the people of Ukraine,” Garland said, adding that the funds were confiscated following an indictment against Malofeyev, issued last April.
Earlier this week, a federal court in New York allowed prosecutors to confiscate $5.4 million belonging to Malofeyev, paving the way for the funds to be used to help rebuild Ukraine.
In June, millions were seized from a US bank account belonging to Malofeyev, against whom the US Treasury Department announced sanctions in April “for having acted or purported to act for or on behalf of, directly or indirectly” the Russian government.
The businessman, who owns Russian Orthodox Christian channel Tsargrad TV, has been on the US sanctions list since 2014. Malofeyev previously claimed that he had no holdings in the West since then.
In December, US President Joe Biden signed legislation allowing the Department of Justice to transfer some forfeited assets to the State Department to aid Ukraine. US law restricts how the government can use such assets.
February 4, 2023
Posted by aletho |
Economics, Russophobia | United States |
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It is a curious thing… the chief claims of feminism used to be that women can run the world better than men, in which peace will abound and everyone will be nice to each other—gone will be toxic masculinity, the root of all evil.
But glancing at the women who have clawed their way to power does not bode well for Pax Feminarum.
Of course, this article is really going out on a limb, because it is recklessly assuming that we all know what a “woman” is. Given recent manifestations of feminine grace and “feminine beauty,” one may well be hard-pressed to hold one’s tongue, as it now appears that men make better women.
But regardless, the now-infamous honesty of Annalena Baerbock caught the righteous off-guard who quickly had to declare that shipping untold weapons and money to the Ukraine, to allow that pitiful country to kill some Russians while also getting itself slaughtered—does not mean that anyone actually wants war. Heavens, no! What insanity. Supplying weapons and cash is one thing. War is, well, quite another! Ms. Baerbock is simply “insane,” everyone happily concluded. Of course, what Ms. Baerbock said was all Russian propaganda. (Here, one can only stand in awe-struck wonder of Russian bots that can now hack into a politician’s brain and force out words that can then be used for “propaganda”).
Not to be outdone, of course, Poland launched its own secret weapon, one Anna Fotyga, who helpfully penned an op-ed, in which she laid out her own brilliant master-plan of dismantling Russia and dividing it up into tiny bits and owning all the natural resources, which can only be best managed by the likes of Ms. Fotyga and her various cronies. To help along this endeavor, Ms. Fortyga has set up proper “team” to get the job done good and right. Premeditated crimes, premeditated war, anyone?
You might be wondering, why should Russia be dismantled by those that know better? Let’s just quote Ms. Fotyga (and please hold back Polish jokes until later):
There are no such things as Russian gas, oil, aluminium, coal, uranium, diamonds, grain, forests, gold, etc. All such resources are Tatar, Bashkir, Siberian, Karelian, Oirat, Circassian, Buryat, Sakha, Ural, Kuban, Nogai, etc. For most of the inhabitants of the regions — be they ethnic Russians or indigenous people — Moscow represents only war, repression, exploitation and hopelessness. Harassment and discrimination against ethnic minorities in Russia is commonplace. Hyper-centralisation has exposed the country’s multiple weaknesses, but foremost, subjugated theoretically autonomous regions and republics to the will of the Kremlin. Moreover, with its odious war of aggression, Moscow is sending ethnic minorities to the meat grinder, implementing a real ethnic policy by further harming both the Ukrainian and already conquered nations of the Far East.
In other words, Ms. Fotyga wants to do exactly what she says are “Russian crimes”—taking other people’s stuff. The rationale for all this, you might wonder? Well, here’s the headline to the article: “The dissolution of the Russian Federation is a far less dangerous than leaving it ruled by criminals.”
What she herself is planning are not crimes, because only Russians can be dangerous criminals. Polish politicians… not so much.
And wonder what does she really mean by “dangerous?” And how does she really understand “criminality?” “Dissolution”—the Final Solution? But among her cronies, saying “Russians” is explanation enough. You see, in Ms. Fotyga’s version of the world, the Russians by nature are beastly criminals and don’t deserve to have a country, let alone live, since they took it all from other people anyway. Dissolution!
One might want to ask Ms. Fotyga whether she’s considering returning any of the “wealth” stolen by Poles from the indigenous people that once lived on the real estate that she and her ilk so presumptuously call “Poland?” As an example, why not first break up Poland and give it back to the Vlachs, the Avars, the Scythians, the Balts, the Sarmatians, the Celts, and heck, even the Germans, all of whom lived in this area long before the Polans, a tribe of Slavs, decided to show up in the 7th century AD. And true to form, the Polans went ballistic and killed everyone, so they could steal their land. Thus, the ancestors of Ms. Fotyga were busy being horrible colonialists, using genocide and conquest to their advantage. Yes, “dangerous” “criminals.” The dissolution of Poland is far less dangerous than leaving it ruled by criminals.
Given the “moral” outrage at Russia, it is high time that Poland led by example. For starters, the worthy team, “European Conservatives and Reformists,” might want to put together a working group that will trace the descendants of the aforesaid indigenous peoples of Poland and start making reparations. It’s high time for a Polish version of Truth and Reconciliation, to pay for the crimes of the Polans. By the way, lots of cash is always a good way to begin. (By the way, how the heck can you be a “conservative” and a “reformist?”)
While all that is taking shape, these Polish politicians might also wish to explain why in a poll conducted in 2011, a lot of people living in Poland decided that they were not going to identify as “Polish.” Wonder why that is? Truth and Reconciliation.
Here, it is necessary to say that this is not about ordinary Polish people, who are being ruled over by warmongers—just as in every other Western country, where politicians are a tribe all their own, who rule against the people that they supposedly work for. But let’s not digress.
Now, we all know the real reason for Ms. Fotyga’s dreams of conquest and plunder. Her fellow countryman, one Mr. Brzezinski, also had the same dream, and he imagined that he could convince America to be the hacksaw that would hack apart Russia and let Poland be the Gauleiter-in-chief of the “eastern lands.” In other words, Poland wants to get its hands on all those resources that Russia has via the USA. See “criminality” above.
And so, Poland wants to transform the war in the Ukraine into pure banditry aimed further East—yes, exactly what the Polans did to the area now known as “Poland.” The apple does not fall far from the tree.
The only problem with this pipedream is that Ms. Fotyga and her band of self-righteous looters are relying on old Uncle Joe who, granted, has a lot to bury in the Ukraine. But as he just outplayed Scholz of Germany with tanks, let’s not get too carried away, would be sane advice to Poland. Joe isn’t as foolish as he appears, that is, his handlers aren’t.
By the way, why is everyone dutifully calling the tanks the Germans will be sending to the Ukraine “Leopards?” And why are the earlier versions of these tanks that went into the same region, back in the day, in the 1940s, always called “Panzers?” Remember the Panzerlied? In 2023, Panzers are not “Panzers,” because they’re “Leopards,” which in German is Panzers. Got that? Yes, because gender is fluid.
But why does the current crop of female politicians love war so much? Keep in mind, the entire Ukraine mess is the creation of one Victoria Nuland, of “F*** the EU!” fame, and who also could not help but gloat recently, when she remembered what happened to the Nord Stream 2 pipeline…
So, the rumors are true—Poles got the go-ahead from her to blow up the pipelines, and dutifully did?
There was another woman, with thwarted presidential ambitions, who gloated and cackled at the horrendous murder of Muamar Kaddafi, she of the “We came, we saw, he died” fame. But let’s go down that rabbit hole.
Polish politicians actually thinks such people are their friends? How deluded do you have to be?
But let’s go back to where we began. Whatever happened to that feminist claim that women will manage the world far better than men? There is an old trope in folktales the world over—of the evil step-mother. That is who these women politicians are — our evil step-mothers.
As for Poland, back in the day, the Poles assumed that they had finally found the perfect friend in this world. Old Adolf Hitler himself and they were going to pal up to him and use the Germans to destroy the Russians. We all know how that turned out. Well, it’s the same pipe dream again; and to show Uncle Joe that this time Poland means business, they are arming themselves to the hilt, because you know, Russians—and all that loot, just yours for the taking. Just replace Adolf with Joe Biden. And the conniving strategy is to draw America in so deep into the Ukraine that withdrawal will become impossible and then the fun can really begin. How quickly people forget Afghanistan…
Ok, break out the Polish jokes.
And, please God, deliver us all from evil step-mothers.
Thane Angus writes from a small northern Canadian town.
February 4, 2023
Posted by aletho |
Russophobia | Poland |
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Top Cardiologist and The HighWire Contributor, Dr. Peter McCullough, was sued by health giant Baylor Scott & White, over an alleged violation of his separation agreement. On January 23rd, a Dallas County District Court dismissed the case with prejudice. Del announces the development, and offers his thoughts as well as congratulations to Dr. McCullough over the ‘win for freedom.’
The Highwire with Del Bigtree | February 2, 2023
The Covid emergency is over in America… in three more months says the White House. Why now? Is politics at the heart of this decision? And what does it mean for the EUA vaccines and therapies? The HighWire gets to the facts behind the headlines.
February 4, 2023
Posted by aletho |
Science and Pseudo-Science, Video | Covid-19, COVID-19 Vaccine, United States |
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WASHINGTON – A former US defense official told Sputnik it is hard to imagine why China would risk sending an uncontrollable balloon with high-end surveillance equipment over the United States.
The Pentagon on Friday said it detected another Chinese surveillance balloon – this one transiting Latin America, which comes a day after the US identified the first one over Montana.
Beijing said the balloon over the US is a civilian airship intended for scientific research, however, Secretary of State Antony Blinken scrapped a high profile visit to China over the incident.
“It is hard to imagine why the Chinese would risk sending military-grade surveillance equipment in a vulnerable, uncontrollable balloon that cannot even be directed to a specific target,” former Pentagon analyst Chuck Spinney said. “These high altitude balloons basically go with the wind-flows.”
US constitutional historian and political commentator Dan Lazare said the US response has been a gross overreaction. Canceling an important diplomatic trip over something as trivial as this is absurd, he added.
China’s foreign ministry on Friday said the airship deviated far from its planned course and regrets the unintended entry into US airspace due to force majeure.
February 3, 2023
Posted by aletho |
Aletho News | China, United States |
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RT DE Productions – a German-based company that produces content for the RT DE TV channel and website in Moscow – has announced that it’s halting all its operations in the country. The company cited “the repressive state of media freedoms within the EU.”
The latest round of sanctions adopted by Brussels has made any further activities of the company in Germany impossible, RT DE Productions said in a statement on Friday.
The ninth sanctions package introduced in December 2022 amounted to “effectively cutting off oxygen for staff,” the firm said, adding that the EU had “betrayed the reliance on the fundamental rights and freedoms recognized in the Charter of Fundamental Rights” of the bloc itself.
“The EU, in permitting the imposition of sanctions on media freedoms, has shown that the very values claimed to define the core of its existence are without any substance,” the statement read, adding that the freedom of the press “does not exist in Germany today.”
The production company also said it was “happy and proud” to be able to provide German-speaking audiences in multiple countries with “essential stories and opinions, often side-lined or overlooked by the mainstream media outlets.”
The sanctions package announced in December blacklisted RT’s parent company, TV-Novosti, as well as revoking the EU broadcasting licenses of Russian media outlets including NTV, NTV Mir, Rossiya 1, REN TV and Perviy Channel. Following the introduction of these new restrictions, Paris froze the accounts of RT France, citing the need to comply with the new regulations. The move forced RT’s French subsidiary to cease broadcasting.
Even before the conflict in Ukraine, RT had faced multiple obstacles to launching a live TV channel for a German audience back in 2021. German banks abruptly refused to work with the broadcaster, and Luxembourg shot down its licensing bid.
When the channel was eventually launched in December 2021, its YouTube page was immediately banned and European satellite TV operator Eutelsat took it off air shortly after, giving in to pressure from the German media regulator, MAAB. The regulator then demanded a broadcast ban on the RT DE channel, accusing RT DE Productions of broadcasting without a valid German license.
RT DE Productions is not a broadcaster, but a production company, while the RT DE channel was broadcast from Moscow under a valid EU-wide Serbian license. However, a German court sided with the media regulator in March 2022.
February 3, 2023
Posted by aletho |
Civil Liberties, Full Spectrum Dominance, Russophobia | European Union, France, Germany |
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A strange Job Posting

The UK Health Security Agency (UKHSA) is currently advertising to recruit an individual for the position of “Vaccine Supply Operation Lead”. You have until 14th February 2023 to apply and can earn up to £62,286 (USD $76,174).
Nothing strange about that so far so why am I writing a post about it?

The weird part comes in the description about the job. In the ‘Job summary’ section it says the following: (emphasis my own)
The role of Vaccine Supply Operations Lead is a new post to support the operations, providing accurate and timely reports for a range of stakeholders during what is expected to be the UK’s largest vaccination programme which will be delivered at pace and will be a key Ministerial priority. The role will be directly responsible for the daily operational management of all covid related products, ensuring their timely distribution across the UK, Crown Dependencies, and Overseas Territories.
“The UK’s largest vaccination programme which will be delivered at pace and will be a key Ministerial priority.” Surely no vaccination programme could be larger than the Covid one? What could they be talking about?
As I see it, there are three possible explanations for this ominous sounding job description:
- The most obvious and likely reason is that the UKHSA have been sloppy. They have recruited someone to write an advert who is lazy, recycled previous material from the pandemic and hasn’t checked their work. However, I have tried to find a previous job description from which the wording may have been taken but with no luck so far. Furthermore, this posting has been up for a few days now, so you would think that any mistake would have been highlighted and corrected. When searching for the job, it is the third paragraph in the job summary, so not something buried away in mountains of text.
- The second reason is that someone in the UKHSA is trolling people like me who have been suspicious about the mRNA roll out. This may sound unlikely but they have recent form in this area. At the beginning of the pandemic, someone in the Civil Service who had clearly had enough, tweeted the following about the government.

- And the third and least likely reason is that the UKHSA are aware of some reason why a massive vaccination campaign may need to start up again. Whilst the least likely of the three options, it would be unwise to dismiss the idea completely.
February 3, 2023
Posted by aletho |
Civil Liberties, Deception | Covid-19, UK |
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The inside story of how we held Pfizer to account for misleading parents about Covid vaccine safety

Free pass promotional opportunity given by BBC to Pfizer
On 2 December 2021, the BBC published on its website, its popular news app and in the BBC News at One programme, a video interview and an accompanying article under the headline ‘Pfizer boss: Annual Covid jabs for years to come’.
The interview by the BBC’s medical editor, Fergus Walsh, conducted as a friendly fireside chat, gave Dr Albert Bourla, the Chairman and CEO of Pfizer, a free pass promotional opportunity that money cannot buy — as the UK’s national public service broadcaster, the BBC is usually prohibited from carrying commercial advertising or product placement.
Perhaps unsurprisingly, Pfizer made the most of that astonishing opportunity to promote the uptake of its vaccine product. As the BBC’s strapline suggests, the key message relayed by Dr Bourla, responding to an obediently leading question from Mr Walsh, was that many more vaccine shots would need to be bought and jabbed to maintain high levels of protection in the UK. He was speaking shortly before the UK Government bought another 54 million doses of Pfizer vaccines.
Misleading statements about safety
Among his explicit and implicit encouragements for the UK to order more of his company’s shots, Dr Bourla commented emphatically about the merits of vaccinating children under 12 years of age, saying “[So] there is no doubt in my mind that the benefits, completely are in favour of doing it [vaccinating 5 to 11 year olds in the UK and Europe]”. No mention of risks or potential adverse events, nor indeed the weighing of any factors other than apparent benefits: Dr Bourla was straightforwardly convinced that we should immunise millions more children in the UK. In fact, it later emerged that the BBC’s article had misquoted Dr Bourla who in the full video interview recording had ventured the benefits to be “completely completely” in favour of vaccinating young children.
Despite the strength of Dr Bourla’s unconditional and superlative pitch for vaccinating under-12s, the UK regulatory authorities would not authorise the vaccine for use with those children until the very end of 2021; and indeed this came just a few months after the JCVI — the body which advises the Government on whether and when to deploy vaccines in the UK — had already declined to advise the Government to roll out a mass vaccination programme for healthy 12 to 15-year-olds on the basis that “the margin of benefit, based primarily on a health perspective, is considered too small to support advice on a universal programme of vaccination of otherwise healthy 12 to 15-year old children…”.
In response, soon after the interview aired, UsForThem submitted a complaint to the UK’s Prescription Medicines Code of Practice Authority (PMCPA) — the regulator responsible for policing promotions of prescription medicines in the UK. The complaint cited the overtly promotional nature of the BBC’s reports and challenged the compliance of Dr Bourla’s comments about children with the apparently strict rules governing the promotion of medicines in the UK.
A year-long, painful process
More than a year later, following a lengthy assessment process and an equally lengthy appeal by Pfizer of the PMCPA’s initial damning findings, the complaint and all of the PMCPA’s findings have been made public in a case report published on the regulator’s website.** Though some aspects of that complaint ultimately were not upheld on appeal, importantly an industry-appointed appeal board affirmed the PMCPA’s original findings that Dr Bourla’s comments on vaccinating 5 to 11-year-olds were promotional, and were both misleading and incapable of substantiation in relation to the safety of vaccinating that age group.
Even after UsForThem involved a number of prominent Parliamentarians, including Sir Graham Brady MP, to help accelerate the complaint, the process was dragged on — or perhaps ‘out’ — while the roll-out of Pfizer’s vaccine to UK under-12s proceeded, and the BBC’s interview and article stayed online. Even now the interview remains available on the BBC’s website, despite the PMCPA in effect having characterised it as ‘misinformation’ as far as vaccinating children is concerned.
When news of the appeal outcome was first revealed in November 2022 by a reporter at The Daily Telegraph newspaper, Pfizer issued a comment to the effect that it takes compliance seriously and was pleased that the “most serious” of the PMCPA’s initial findings — that Pfizer had failed to maintain high standards and had brought discredit upon and lowered confidence in the pharmaceutical industry — had been overturned on appeal.
It must be an insular and self-regarding world that Pfizer inhabits, that discrediting the pharmaceutical industry is considered a more serious matter than making misleading and unsubstantiated statements about the safety of their products for use with children. This surely speaks volumes about the mindset and priorities of the senior executives at companies such as Pfizer.
And if misleading parents about the safety of a vaccine product for use with children does not discredit or reduce confidence in the pharmaceutical industry, it is hard to imagine what standard can have been applied by the appeal board which overturned that initial finding. Perhaps this reflects the industry’s assessment of its own current reputation: that misinformation promulgated by one of its most senior executives is not discrediting. According to the case report, the appeal board had regard to the “unique circumstances” of the pandemic: so perhaps the view was that Pfizer can’t always be expected to observe the rules when it gets busy.
Multiple breaches. No meaningful penalty
Indeed, a brief look at the PMCPA’s complaints log confirms that Pfizer has been found to have broken the UK medicines advertising rules in relation to its Covid vaccine a further four times since 2020. Astonishingly, though, for their breaches in this most recent case, and in each of the other cases decided against it, neither Pfizer nor Dr Bourla will suffer any meaningful penalty (the PMCPA will have levied a small administrative charge to cover the cost of administering each complaint). So in practice, neither has any incentive to regret the breach, or to avoid repeating it if it remains commercially expedient to do so.
And this is perhaps the crux of the issue: the PMCPA, the key UK regulator in this area, operates as a division of the Association of the British Pharmaceutical Industry, the UK industry’s trade body. It is therefore a regulator funded by, and which exists only by the will of, the companies whose behaviour it is charged with overseeing. Despite Pharma being one of the most lucrative and well-funded sectors of the business world, the largely self-regulatory system on which the industry has now for decades had the privilege to rely has been under-resourced and has become slow, meek and powerless.
The UK Medicines and Healthcare Products Regulatory Agency (MHRA) in principle has jurisdiction to hold the BBC accountable for what seems likely to have been mirroring breaches of the medicines advertising rules when it broadcast and promoted Dr Bourla’s comments, but no action has yet been taken.
This case, and the apparent impunity that companies such as Pfizer appear to enjoy, evidence that the system of oversight for UK Pharma is hopelessly outdated and that the regulatory authorities are risibly ill-equipped to keep powerful, hugely well-resourced corporate groups in check. The UK regulatory system for Big Pharma is not fit for purpose, so it is time for a rethink. Children deserve better, and we should all demand it.
** Endnote: an undisclosed briefing document
As part of its defence of UsForThem’s complaint, Pfizer relied on the content of an internal briefing document that had been prepared for the CEO by Pfizer’s UK compliance team before the BBC interview took place. Pfizer initially asked for that document to be withheld from UsForThem on the grounds that it was confidential. When UsForThem later demanded sight of the document (on the basis that it was not possible to respond fully to Pfizer’s appeal without it), UsForThem was offered a partially redacted version, and only then under terms of a perpetual and blanket confidentiality undertaking.
Without knowing the content of that document, or the scope of the redactions, UsForThem was unwilling to give an unconditional perpetual blanket confidentiality undertaking, but reluctantly agreed that it would accept the redacted document and keep it confidential subject to one limited exception: if UsForThem reasonably believed the redacted document revealed evidence of serious negligence or wrongdoing by Pfizer or any other person, including evidence of reckless or wilful damage to the public health of children, UsForThem would be permitted to share the document, on a confidential basis, with members of the UK Parliament.
This limited exception to confidentiality was not accepted. Consequently, UsForThem never saw the briefing document and instead drew the inference that it contained content that Pfizer regarded as compromising and which it therefore did not wish to risk ever becoming public.
February 3, 2023
Posted by aletho |
Deception, Fake News, Mainstream Media, Warmongering | BBC, COVID-19 Vaccine, Pfizer, UK |
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Merck’s oral antiviral pill for COVID-19, molnupiravir — marketed under the name Lagevrio — may be fueling the development of new and potentially deadly variants of COVID-19, according to the authors of a new preprint study.
The study, released Jan. 27 by a team of U.S. and U.K researchers, found, “It is possible that some patients treated with molnupiravir might not fully clear SARS-CoV-2 infections, with the potential for onward transmission of molnupiravir-mutated viruses.”
Merck received significant taxpayer funding from the Biden administration to develop and distribute molnupiravir, and the U.S. government bought nearly 2 million courses of the drug on the taxpayer’s dime.
The study, which is pending peer review, followed the discovery by a middle school science and math teacher in Indiana who found numerous variants of COVID-19 emerged after molnupiravir began to be widely distributed.
Scientists had long warned that the development of such mutations from the use of molnupiravir was possible.
“It’s not a surprise that molnupiravir could cause [the] escape of mutant virus strains or substrains into the population,” said Dr. Harvey Risch. “Its main function is to get the virus to mutate faster.”
Risch, professor emeritus and senior research scientist in epidemiology (chronic diseases) at the Yale School of Public Health, told The Defender :
“The idea is that it will mutate itself to death. But some live mutants could get out, and this paper gives evidence that they have.”
Brian Hooker, Ph.D., P.E., chief scientific officer for Children’s Health Defense, said the study’s authors scanned global SARS-CoV-2 sequence databases looking for mutations characteristic of those by molnupiravir (G-to-A and C-to-U) and found an uptick of those mutants starting in 2022 — after molnupiravir was put on the market and specifically in countries where molnupiravir was distributed.
“Although this isn’t ‘direct proof’ that the mutations came directly from molnupiravir use,” Hooker told The Defender, “the evidence is very compelling, confirming the fears of many who warned of this prior to FDA [U.S. Food and Drug Administration] approval of the drug in late 2021.”
The FDA granted molnupiravir Emergency Use Authorization (EUA) on Dec. 23, 2021, for use in mild-to-moderate COVID-19 infections in patients 18 and over.
The EUA came just one day after the FDA authorized Pfizer’s COVID-19 antiviral treatment Paxlovid.
Merck this week announced massive revenues from sales of molnupiravir in 2022, but projected a significant decrease in those sales in 2023.
The FDA on Wednesday removed the requirement that a person has to test positive for COVID-19 in order to get a prescription for molnupiravir or Paxlovid.
‘I think we are courting disaster’
Molnupiravir “works by creating mutations in the COVID-19 genome that prevent the virus from replicating in the body, reducing the chances it will cause severe illness,” according to Bloomberg.
However, according to Science, the findings of the preprint study suggest “some people treated with the drug generate novel viruses that not only remain viable, but spread.”
This finding “underscores the risk of trying to intentionally alter the pathogen’s genetic code,” leading some researchers to “worry the drug may create more contagious or health-threatening variations of COVID,” Bloomberg reported.
Virologist William Haseltine, Ph.D., chair and president of ACCESS Health International, has repeatedly raised such concerns about molnupiravir.
“It’s very clear that viable mutant viruses can survive [molnupiravir treatment] and compete [with existing variants],” Haseltine told Science. “I think we are courting disaster.”
According to the Gateway Pundit, “When one studies how Lagevrio works, this should not come as a shock. The pill attacks the COVID virus by trying to alter its genetic code.”
The Gateway Pundit reported:
“Once inside a human cell, a virus can make 10,000 copies of its genetic code in a few hours. Each copy made increases the risk the virus makes a rare mistake and creates an inexact replica.
“This is how mutations happen as we have seen with COVID. A drug that deliberately alters a virus’s genetic code would greatly increase the mutation risk.”
Dr. Jonathan Li, a virologist and the director of Li Laboratory, associated with Harvard Medical School and Brigham and Women’s Hospital, told Bloomberg :
“There’s always been this underlying concern that it could contribute to a problem generating new variants. This has largely been hypothetical, but this preprint validates a lot of those concerns.”
According to Science, Haseltine and other scientists have long worried that molnupiravir would create COVID-19 mutations that “would survive and propagate — and perhaps turn out to be more transmissible or virulent than before.”
A Merck spokesperson described that theory as “an interesting hypothetical concern,” prior to the drug receiving EUA.
The same scientists also worried that aside from the virus, the DNA of those receiving the drug might also mutate, Science reported.
These concerns led “researchers and citizen scientists” to examine COVID-19 genome sequences cataloged in the international GISAID (Global Initiative on Sharing Avian Influenza Data) database, seeking to identify mutations likely to be caused by molnupiravir.
‘Clearly something is happening here’
Searching for these mutations was based on the premise that, “Rather than inducing random changes in the virus’ RNA genome, [molnupiravir] is more likely to cause specific nucleic acid substitutions, with guanine switching to adenine and cytosine to uracil,” added Science.
Through this process, Ryan Hisner, a middle school science and math teacher from Monroe, Indiana — described by Science as a “virus hunter” — ultimately “identified dozens of sequences that showed clusters of those hallmark substitutions.”
Hisner took to Twitter with his concerns, where he came into contact with Thomas Peacock, Ph.D., a virologist at the Imperial College London. They and other U.K. and U.S. researchers “systematically reviewed more than 13 million SARS-CoV-2 sequences in GISAID and analyzed those with clusters of more than 20 mutations,” according to Science.
The team found “a large subset showed the hallmark substitutions; all dated from 2022, after molnupiravir began to be widely used,” Science reported.
According to the preprint study, Molnupiravir, “acts by inducing mutations in the virus genome during replication. Most random mutations are likely to be deleterious to the virus, and many will be lethal.”
However, the researchers wrote:
“It is possible that some patients treated with molnupiravir might not fully clear SARS-CoV-2 infections, with the potential for onward transmission of molnupiravir-mutated viruses.
“We set out to systematically investigate global sequencing databases for a signature of molnupiravir mutagenesis. We find that a specific class of long phylogenetic branches appear almost exclusively in sequences from 2022, after the introduction of molnupiravir treatment, and in countries and age groups with widespread usage of the drug.
“Our data suggest a signature of molnupiravir mutagenesis can be seen in global sequencing databases, in some cases with onwards transmission.”
Peacock told Science these “signature clusters” were up to 100 times more likely to be identified in countries where molnupiravir was widely used, including the U.S., U.K. and Australia, as compared to countries such as Canada and France, where it was not in widespread use.
“Clearly something is happening here,” said Peacock.
Merck: ‘no evidence’ any antiviral agent has contributed to the emergence of circulating variants’
Theo Sanderson, Ph.D., a geneticist at the Francis Crick Institute and co-author of the preprint, told Science “We are not coming to a conclusion about risk” just yet, with regard to whether or not these mutations may lead to more severe COVID-19 variants.
Indeed, according to the preprint study, the variants identified by the researchers have not been shown to be more lethal or more evasive to immunity than other existing strains of COVID-19.
However, Haseltine illustrated the potential risk via the analogy of owning a pet lion: “Just because it didn’t bite you yesterday doesn’t mean it won’t bite you today.”
According to the Gateway Pundit :
“Merck was warned by multiple scientists their drug might create problematic mutations which would render the virus more dangerous and difficult to treat. The company decided to blow off any concerns and put Lagevrio [molnupiravir] on the market anyway.”
As previously reported by The Defender, Dr. James Hildreth, president and CEO of Meharry Medical College and member of Biden’s COVID-19 Health Equity Task Force, expressed concerns about mutant variants escaping.
In 2021, Hildreth told an FDA advisory panel, “Even if the probability is very low, one in 10,000 or 100,000, that this drug would induce an escape mutant from which the vaccines we have do not cover, that could be catastrophic for the whole world actually.”
Also in 2021, Haseltine told Science :
“You are putting a drug into circulation that is a potent mutagen at a time when we are deeply concerned about new variants. I can’t imagine doing anything more dangerous.
“If I were trying to create a new and more dangerous virus in humans, I would feed a subclinical dose [of molnupiravir] to people infected.”
Two other recent studies also called out molnupiravir, questioning its effectiveness and raising concerns the drug may help lead to the development of new COVID-19 variants.
A December 2022 preprint by a team of Australian researchers, found “this commonly used antiviral can ‘supercharge’ viral evolution in immunocompromised patients, potentially generating new variants and prolonging the pandemic.”
And a study published Jan. 28 in The Lancet found, “Molnupiravir did not reduce the frequency of COVID-19-associated hospitalisations or death among high-risk vaccinated adults in the community.”
University of Cambridge clinical microbiologist Ravindra Gupta, Ph.D., told Science that while it’s unclear whether molnupiravir will cause deadlier COVID-19 variants, the overall results of these recent studies “call into question whether molnupiravir should be used.”
Merck spokesperson Robert Josephson defended the product, telling Bloomberg, “There is no evidence that any antiviral agent has contributed to the emergence of circulating variants.”
Molnupiravir ‘different’ than Paxlovid — and ‘riskier’
Although molnupiravir is similar to Paxlovid in that both are oral antiviral treatments for COVID-19, Hooker told The Defender there are significant differences in how the two drugs work:
“Molnupiravir acts on the SARS-CoV-2 virus by directly inducing mutations in the RNA genome. This is a completely different mode of action compared to Pfizer’s product, Paxlovid, and in my estimation is quite dangerous.
“Merck claimed the mutation rate induced by molnupiravir would kill the virus and that mutants wouldn’t escape, but that has been shown to be false in studies of immunocompromised patients.”
Hooker said Paxlovid — and the COVID-19 vaccines — can potentially lead to the development of mutations as well.
But in his view, the “mechanism of action” used by molnupiravir is different — and far riskier — than Paxlovid and COVID-19 vaccines, which merely increase the virus’ lifetime in the human body, giving the virus a greater opportunity to naturally mutate.
Hooker said:
“In contrast, molnupiravir directly induces mutations and thereby vastly increases the mutation rate of the virus in the human host.
“In my estimation, this is a very dangerous way to treat such an infection, given the implications of creating random mutants.”
Merck made billions from molnupiravir — thanks to taxpayers
In 2022, sales of Merck’s molnupiravir hit $5.68 billion, fueled in part by strong fourth-quarter sales of the drug in Asia.
Fourth-quarter sales of molnupiravir reached $825 million, more than doubling analyst expectations of $358 million.
These strong earnings were boosted by government — or taxpayer — support.
In June 2021 — with molnupiravir still in clinical trials, which weren’t completed until October 2021 — the federal government signed a $1.2 billion contract with Merck for 1.7 million courses of the drug, at a cost of approximately $712 per patient.
An analysis by Melissa Barber of the Harvard T.H. Chan School of Public Health and Dzintars Gotham of King’s College Hospital in London found the cost of production of molnupiravir was approximately $1.74 per unit — or $17.74 for a five-day regimen.
By those calculations, the U.S. government paid a near-4,000% markup.
In March 2022, during his State of the Union address, President Biden announced the “Test to Treat” initiative, which allowed those who tested positive for COVID-19 at a pharmacy to obtain free antiviral pills — including molnupiravir — on the spot.
One month earlier, the Biden administration had proceeded with a new purchase of 3.1 million courses of molnupiravir, with the option to purchase more.
Estimates for Merck, and other COVID-19 drugmakers, are less rosy for 2023, as the public tires of all things pandemic and Biden looks to end the COVID-19 national emergency in May.
According to Reuters, sales of molnupiravir are expected to fall to about $1 billion this year, contributing to an expected decline in sales for Merck from $59.3 billion in 2022 to $57.2-$58.7 billion this year.
Merck’s stock price dropped by about 2% with Thursday’s announcement.
Despite these large earnings, overall sales of molnupiravir lagged significantly behind Paxlovid in 2022. Sales of Paxlovid reached $18.9 billion last year.
Michael Nevradakis, Ph.D., based in Athens, Greece, is a senior reporter for The Defender and part of the rotation of hosts for CHD.TV’s “Good Morning CHD.”
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
February 3, 2023
Posted by aletho |
Science and Pseudo-Science | Covid-19, FDA, Joe Biden, Lagevrio, Merck, Molnupiravir, United States |
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