2020: Annus Horribilis, The Worst Is Yet to Come? Poverty, Unemployment, Despair
By Stephen Lendman | January 1, 2021
For most Americans, 2020 was disastrous for their safety, well-being and future.
Unprecedented numbers of people lost jobs — a greater percent of working-age Americans than in the 1930s Great Depression.
Millions more became way underemployed earning poverty wages with few or no benefits — struggling daily to survive.
Well over 100,000 small businesses went bankrupt or otherwise shut down permanently because of draconian lockdowns, quarantines and related policies.
According to Gallup survey data, “Americans’ mental health ratings s(ank) to a new low” in 2020 — with no end to mass-misery in prospect.
Chicago’s Water Tower Place is the city’s preeminent downtown shopping mall along its Magnificent Mile.
Its survival is threatened by lack of enough retail traffic.
A city news report said there’s “real anxiety that Chicago’s main shopping districts — the Magnificent Mile and Gold Coast — are (at risk) of falling apart” for lack of enough revenue to keep operating.
The Illinois Retail Merchants Association said “economic fallout” from what’s going on “made it difficult for businesses to keep up with high downtown rents.”
What’s true about Chicago’s retail environment applies to the US nationwide — with no end of it in prospect looking ahead.
According to the National Restaurant Association, up to half of the nation’s restaurants may close permanently if the current environment continues or worsens — millions of jobs to be lost with them.
Looking ahead in the new year, is unprecedented food insecurity, hunger, malnutrition, untreated illnesses, and homelessness coming in the weeks and months ahead?
While Congress and the Wall Street owned and controlled Fed throw trillions of dollars of free money at the nation’s privileged class, most US households never endured harder than ever hard times than now.
They’re worsening, not improving, because of indifference in high places toward the nation’s most disadvantaged that are exploding in numbers of affected millions of people — the US middle class disappearing in plain sight.
Everything going on — the Greatest Main Street Depression in US history — was planned by US dark forces in cahoots with monied interests.
It’s all about benefitting them exclusively by exploiting most others.
It includes creating an unprecedented in size permanent underclass.
Longer-term, the diabolical scheme aims to create a ruler-serf society, harming the vast majority of Americans.
Seasonal flu/influenza — disguised as covid — has been and continues to be the phony pretext for getting Americans to go along with what no one should tolerate.
Their fundamental freedoms may be permanently lost so privileged interests can more greatly benefit from their misery.
Providing $600 stimulus checks to qualified households pales in comparison to open-checkbook handouts to Wall Street, other corporate favorites, and the already super-rich.
The paltry amount mocks growing poverty and deprivation that’s highly likely to worsen in the new year.
The US is not only unsafe and unfit to live in, it’s permanently thirdworldized.
It’s a totalitarian/plutocratic banana republic in the Northern Hemisphere — the world’s largest and most threatening to everyone everywhere.
On New Year’s Day, establishment media maintained their mass deception drumbeat.
According to NYT fake news, “in 2021 things will start getting better (sic).”
“And there’s good reason to believe that once the good news starts, the improvement in our condition will be much faster and continue much longer than many people expect (sic).”
The Washington Post pretended that “the big story of 2021 could be a very hopeful one (sic).”
Like other establishment media, it’s pushing the myth of mass-vaxxing to the rescue — ignoring how experimental covid vaccines may cause irreparable harm to human health overall, along with risking the illness they’re supposed to protect against but won’t.
According to the Wall Street Journal, “(t)he great comeback of 2021 is surely coming (sic).”
“(I)t will begin to explode in late spring, with vaccines more available and a spreading sense that things are easing off, and be fully anarchic by summer (sic).”
The above disinformation ignores the reality of unprecedented/made-in-the USA misery that’s highly likely to worsen ahead and become permanent for most Americans.
I see nothing to be optimistic about in the new year and what follows.
The only solution is popular revolution. Nothing else can prevent state-sponsored dystopia that’s well underway.
It’ll worsen without mass outrage and rebellion against the diabolical system.
It’s our lives, our well-being, our future, and our choice to accept the unacceptable or rise up against it.
Navalny and Handlers Lose the Plot… He Is a Convicted Felon on Probation
By Finian Cunningham | Strategic Culture Foundation | January 2, 2021
Russia’s federal prison authorities were right to jolt Alexei Navalny this week by warning him to return immediately from Germany or else face a suspended sentence being made into jail time.
The “professional” opposition activist claims to be convalescing in Germany after he was allegedly poisoned by a Soviet-era nerve agent in August. Western news media dutifully repeat the claim that Navalny is “recuperating” in Germany after having survived an assassination plot by Kremlin agents. Navalny has personally accused Russia’s President Vladimir Putin of ordering the alleged hit.
Last week, a team of medics from the Berlin hospital where Navalny had been staying published a paper in The Lancet medical journal in which they claimed he had been poisoned with Novichok nerve agent. Their findings are dubious because the medics acknowledged the involvement of German military intelligence laboratories in conducting their analysis.
But one thing the German doctors did let slip was that a 55-day follow-up check on Navalny ascertained that he had made a “near-complete recovery”.
The Russian dissident figure was flown to Berlin on August 22, two days after he was treated in a hospital in Omsk, Russia. Thus, the German medical team are indicating – no doubt inadvertently – that Navalny’s health recovered nearly two months ago, if not before that.
That means there is no medical reason why he should remain at large in Germany. His claims of “convalescing” and the Western media’s indulgence of those claims are false, if the German doctors are correct about his “recovery”.
Despite Navalny’s arrogant disdain for Russian state laws, he is nevertheless answerable to those authorities as a citizen. While in Germany he was on probation for a suspended jail sentence concerning a fraud conviction in 2014. His so-called Anti-Corruption Foundation (FBK) has a checkered history of shady financing, from allegations of foreign funding by the U.S. State Department to charges of embezzling millions of dollars. Ironically, the blogger and media activist produces slick programs accusing the Russian government of corruption.
In any case, under the laws of the Russian Federation, the 44-year-old Navalny was on probation during the past four months of his stay in Germany. For the last two months, he is in good health, according to his German doctors. So there are no grounds for why he should abscond from Russian territory and evade the laws for which he is answerable.
Not only is Navalny living as if he above the law, he has also shown flagrant contempt for the Russian authorities.
Last week, he published a video on his website claiming that he had pranked a named member of Russia’s security service, the FSB, into admitting that agents had poisoned him while he was visiting the Siberian city of Tomsk on August 20. He was later flown in an emergency to Omsk where he was treated after having apparently fallen ill onboard a flight to Moscow.
The FSB dismissed Navalny’s prank telephone claim as a “deep fake”. The Russian doctors who treated him in Omsk – and who probably saved his life – have repeatedly stated that their tests showed there was no poison in Navalny’s body, and specifically no traces of nerve agent. They said his illness was due to a metabolic disorder. Perhaps self-induced as a ruse to later transfer to Germany?
The transcript of Navalny’s purported prank call to the FSB agent reads like a comic set-up. Posing as a senior member of Russia’s national security council, Navalny affects to bully the supposed agent as if he is a pathetic stooge.
A telling segment is where the self-styled super sleuth fishes for compliments about his own character from the purported FSB man, betraying the narcissism of a megalomaniac.
Again, incredibly, we are expected to believe that someone who had a near-death experience with a lethal nerve poison and who is “convalescing” still in Germany somehow managed to find the energy and mental reserves to pull off a daring 45-minute telephone sting.
If Navalny is fit enough to participate in such practical jokes – regardless of their credibility – then he is surely fit enough to abide by Russian laws and respect his probation terms. As the Russian Federal Prison Service stated this week: “The convicted man is not fulfilling all of the obligations placed on him by the court, and is evading the supervision of the Criminal Inspectorate.”
One gets the unerring impression that Navalny and his foreign handlers have become so self-intoxicated with hubris that they are blind to their own absurd implausibilities.
Why was he permitted to fly by air ambulance to Berlin in the first place if the Russian authorities had evil designs against him?
While there, as a guest of the German government, Navalny has wildly accused President Putin of ordering his alleged assassination. The European governments have subsequently and rashly imposed sanctions on Russia in support of Navalny’s unfounded claims. Then we have the media activist mounting further provocations parlayed into even more outlandish accusations against President Putin and the Kremlin.
All the while there has been no evidence of poisoning presented to support these claims, other than unverifiable assertions by German doctors working with German military intelligence labs, as well as two other NATO laboratories and the Organization for the Prohibition on Chemical Weapons. All of them including the OPCW (the latter compromised over complicity in NATO false-flag provocations in Syria) have refused to share their analytical data and samples with Russia, and yet they are demanding that Moscow launch a criminal investigation into the Navalny case.
The abdication by European governments of due process and of respect for Russian state laws, its government, and its president is astounding. They are indulging a foreign-sponsored gadfly as if he is the sovereign representative of the Russian Federation.
Navalny and his foreign allies have lost the plot in their own telling of an alleged assassination plot.
First things first: he is a convicted felon who is answerable to Russian law. Pushing false flags and slanderous falsehoods from abroad with the intent of damaging Russia’s sovereignty is an abuse of his rights.
Arrogant and overindulged Navalny is patently incapable of even understanding his obligations under law as a Russian citizen. He evidently feels above the law, like many of his Western backers. That’s why Russia is right to tell him to put up or shut up.
The criminal WHO blows its own cover: fake PCR test
By Jon Rappoport | December 31, 2020
In early 2020, the WHO accepted a PCR test for “SARS-CoV-2” that was designed without having possession of the virus. Yet the test is meant to detect… the missing virus. This is evidence of deep criminal intent. [1]
But as of December 14, 2020, WHO has made a correction [2]. Thereby blowing its own cover. Why?
Two reasons. Huge numbers of people have caught on to the PCR test scam. And by their correction, WHO paves the way for “declining COVID case numbers”—thereby making it appear the new vaccine is a roaring success. I predicted this development. [3] [4]
A brief review. The PCR test (a complete fraud for several reasons) is run in “cycles.” Each cycle is a giant magnification of a tiny portion of the swab sample taken from the patient.
As I’ve reported, even Tony Fauci readily asserts that if the PCR is run at 35 cycles or higher, it’s meaningless. [5] [6]
Every positive result—indicating “infection with the virus”—occurring at 35 cycles or higher is meaningless.
BUT, as I’ve also pointed out, public health agencies recommend running the PCR test at up to 40 cycles. Therefore, labs comply.
Therefore, millions upon millions of PCR tests results, over the last nine months, which indicate “infection,” are a vast lie.
Therefore, the COVID case numbers are a vast lie, and the lockdowns, which are based on those numbers, are absurd, insane, criminal, and predatory.
NOW, the WHO is walking back their stance on how the PCR should be run, for the reasons I mentioned above.
The WHO document is titled, “WHO Information Notice for IVD Users/Nucleic acid testing (NAT) technologies that use real-time polymerase chain reaction (RT-PCR) for detection of SARS-CoV-2.” [2]
Here are the money quotes. The language is mealy-mouthed, intentionally confusing, cautious, and sterile. Nevertheless, we can see the intent to lower the number of test cycles.
“Users of RT-PCR reagents should read the IFU [Information for Use] carefully to determine if manual adjustment of the PCR positivity threshold is necessary to account for any background noise which may lead to a specimen with a high cycle threshold (Ct) value result being interpreted as a positive result.”
Translation: Using too many test cycles—aka “high cycle threshold (Ct) value”—has resulted in patients being told they’re infected, which is a lie.
“In some cases, the IFU will state that the cut-off should be manually adjusted to ensure that specimens with high Ct values are not incorrectly assigned SARS-CoV-2 detected due to background noise.”
Translation: Running the test with a high number of cycles yields “background noise”—aka a false positive result. The patient is told he’s infected but he’s not.
“The design principle of RT-PCR means that for patients with high levels of circulating virus (viral load), relatively few cycles will be needed to detect virus and so the Ct value will be low. Conversely, when specimens return a high Ct value, it means that many cycles were required to detect virus. In some circumstances, the distinction between background noise and actual presence of the target virus is difficult to ascertain.”
Translation: When the test is run with a high number of cycles, we can’t tell the difference between “irrelevant” and “meaningful.”
A frank and honest translation of the WHO message: “We’re changing the way we’re doing PCR tests. We were running them with a high number of cycles and getting millions of false positives, and those numbers were deployed to justify the lockdowns—but NOW we’re moving to a lower number of cycles. This change, all on its own, will result in fewer positive results, fewer case numbers, making the vaccine look VERY GOOD.”
The WHO is still crazy, still criminal, but not entirely stupid. They know what they’re doing and why.
SOURCES:
[1] https://blog.nomorefakenews.com/2020/12/25/you-thought-the-pcr-test-detects-an-actual-virus-wrong/
[2] https://www.who.int/news/item/14-12-2020-who-information-notice-for-ivd-users
[4] https://blog.nomorefakenews.com/2020/11/13/how-theyll-fake-the-success-of-the-covid-vaccine/
[6] https://blog.nomorefakenews.com/2020/12/08/florida-forces-labs-to-report-number-of-pcr-test-cycles/
10 Facts From the UK Government Pfizer Vaccine Guidance that Promote “Vaccine Hesitancy”
By Johnny Vedmore |
Unlimited Hangout| December 29, 2020
Official government guidance has been released in the United Kingdom to assist healthcare professionals in administering the Pfizer/BioNTech vaccine BNT162b2. While the UK government goes to war against supposed misinformation, the official narrative is clearly based on very little to no supporting data from incomplete clinical trials. This article examines the document “Reg 174 Information for UK Healthcare Professionals” and narratives being pushed in the mainstream media that directly contradict that document.
Healthcare professionals globally have begun the controversial campaign to vaccinate large swathes of their respective populations with various experimental medical products. The vanguard of the mainstream pro-vax extremists have been busy enacting mass censorship tactics and committing blatant acts of digital book burning on a scale never before seen in the internet era. So-called “trusted sources” have become indistinguishable from the state-run media apparatus of your bog-standard dictatorship with the usual MSM outlets working non-stop to skew any information that threatens their hyper-aggressive official narrative. Throughout 2020, our basic civil liberties have been quickly stripped away by countless unelected officials from a wide array of unaccountable global power structures, all of them connected to a small group of elites who are sitting aloft the COVID-19 money train and using the heavily exaggerated epidemic to achieve their own long term goals.
Any useful data, scientific paper, or other credible research contradicting the official narrative is being purposely hidden from view. Too many uncomfortable, yet ultimately necessary, questions for vaccine companies such as Moderna, AstraZeneca, Pfizer, and their many collaborators, are being heavily censored by those pushing their own various COVID-related agendas. The promised “war on truth” is in full swing throughout all nations globally and their respective state media machines are nearly all towing their official government lines. Mainstream talk shows and podcasts worldwide are also in lockstep, and have often been caught publicly guilt-tripping their easily swayed audiences to help push them deeper into queues for mass medical trials for vaccines and other products that lack research studies on their long term effects. This inconvenient lack of completed research will not stop the money men from pumping this milky white liquid into the arms of hundreds of millions of people worldwide.
At this point in the process, the medical professionals who are administering these heavily rushed vaccines are being given the opportunity to defer responsibility and accountability for their actions to the government’s vaccine-related guidance. As the Stanley Milgram experiments have proven, when the option to defer responsibility is present, then roughly 65% of participants will follow the orders they have received regardless of the risk to their subjects. In 1974, Stanley Milgram detailed the behaviour of his participants in his famous study and suggested that people have two basic states of behaviour when they are in a social situation: “The autonomous state”, where people direct their own actions and ultimately take responsibility for the results of those actions and “the agentic state”, where people allow others to direct their actions and then pass off the responsibility for the consequences to the person giving orders, in essence acting as agents of another person’s will.
The majority of the people who are injecting these experimental drugs into their trusting patients are not likely to question the official guidance, as the overwhelming majority will often simply be in an agentic state. Thus, it should be in the best interest of anyone thinking of receiving an mRNA vaccine to first study the guidance offered by the various government sources. And, when one does study the official guidance given to healthcare professionals, one will find many different glaring contradictions and shocking admissions.
While all official bodies are attacking any inconvenient fact as misinformation, they are all busy defrauding the global population with their own misinformation campaigns that surely would have inspired awe in the likes of Joseph Stalin. So, let’s study their own words and examine the NHS guidance given to the medical professionals in the UK for the administration of the recently approved Pfizer-BioNTech vaccine.
An Introduction to Reg 174 Information for UK Healthcare Professionals (#1-4)
The short ten page official guidance being given to UK healthcare professionals contains many interesting admissions. In fact, the document, released in early December 2020 to accompany the vaccine rollout, appears to advise healthcare practitioners not to risk giving the experimental injection to the majority of the people who are due to receive the vaccine, particularly “prioritized” populations. Those in charge are pushing to vaccinate as much of the population as possible, before any critical public questions can be asked and answered, a situation that has left the safety and ethics of the vaccination campaign questionable at best and inhumane at worst.
In going through the Reg 174 document, it becomes very clear that there are many issues and recommendations that are being hidden from the general public. Here are ten of the most notable causes for concern contained within the official UK guidance document.
The authorisation to produce and supply this experimental vaccine in the UK was given by the UK Department of Health and Social Care, led by Matt Hancock – the UK Secretary of Health, and also by the Medicines & Healthcare products Regulatory Agency (MHRA). While the MHRA is part funded by the Department of Health and Social Care for the regulation of medical devices, the costs of medicine regulations are met through fees paid by the pharmaceutical industry. The agency’s financial reliance on Big Pharma has led to suggestions by some Members of the UK Parliament that the MHRA is not actually independent. Being in associated roles at the MHRA since 1985, June Raine was officially appointed as CEO in September 2019 and had previously been the Director of Vigilance and Risk Management in the Medicines Division.
2. The official Phase III safety trials will not be completed until 2023
Section 1 of the medical guidance clearly states that this vaccine guidance refers specifically to the “Pfizer/BioNTech COVID-19 mRNA Vaccine BNT162b2 concentrate for solution for injection.” On 2 December 2020, the MHRA became the first medicines regulator in history to approve an mRNA vaccine for human use, granting emergency authorisation for BioNTech and Pfizer’s BNT162b2 COVID-19 vaccine for widespread use only a week after its first Phase III eight-week trial had finished. However, the Phase III trials for BNT162b2 will not actually be fully completed until January 2023 meaning that, if you’re ready to take the vaccine now, then you should be informed that the safety trials for these experimental vaccines have at least two more years before the results are in. Regardless of that fact, Raine told reporters “no corners have been cut in approving it” and that “the benefits outweigh any risk”.
3. Will you be truly “protected” from COVID-19?
The official guidance clearly states that individuals may not be protected until at least 7 days after their second dose of the vaccine. This fact has again been ignored by various reckless pro-vax media campaigns where powerful elites such as Tony Blair have contradicted this specific recommendation, suggesting recently in an interview that people should only be given a single dose of any vaccine. Mr Blair told BBC Radio 4’s Today programme that “Does the first dose give you substantial immunity, and by that I mean over 50 percent effectiveness? If it does, there is a very strong case for not, as it were, holding back doses of the vaccine.” Blair, writing in the Independent, stated that the current vaccination strategy needed to be “altered and radically accelerated”. In responding to Blair’s call for radical acceleration, Professor Wendy Barclay, chair of virology at Imperial College London and member of the UK government’s NERVTAG, said: “I think that the issue with [Mr Blair’s suggestion] is that the vaccine is on the basis of being given in two doses, and the efficacy is on that basis.” Barclay went on to point out that “To change at that point, one would have to see a lot more analysis coming out from perhaps the clinical trial data.”
It is very important to pay attention to the wording of Reg 174 because the Pfizer vaccine purportedly boosts the immune system, rather than stopping the transmission of the virus. This would suggest that you will not be fully “protected” from COVID-19 and that you will still be able to catch the virus and could still suffer complications. The official guidance also states that “Immunocompromised persons, including individuals receiving immunosuppressant therapy, may have a diminished immune response to the vaccine,” with the guidance admitting “No data are available about concomitant use of Immunosuppressants.”
Reg 174 goes on to make this most pertinent of points when it states “As with any vaccine, vaccination with COVID-19 mRNA Vaccine BNT162b2 may not protect all vaccine recipients.” The guidance also states clearly that “administration of COVID-19 mRNA Vaccine BNT162b2 should be postponed in individuals suffering from acute severe febrile illness and that individuals receiving anticoagulant therapy or those with a bleeding disorder that would contraindicate intramuscular injection, should not be given the vaccine unless the potential benefit clearly outweighs the risk.”
4. The complicated multistage dilution and thawing process of the vaccine vials opens the major possibility of human error
In investigating the official instructions for the vaccine’s administration, we can clearly see that there are plenty of opportunities for potential human error. Section 2 of this document describes the distributed vaccine as coming in “a multidose vial and must be diluted before use.” Confirming that each vial contains 0.45 ml (which equates to 5 doses of 30 micrograms) of BNT162b2 RNA embedded in lipid nanoparticles. The delicate preparation process will be repeated 100s of millions of times globally and the multidose vial will be stored frozen and must be thawed prior to dilution. The guidance describes the process for preparing the frozen vials stating that they should be transferred to temperatures of between 2 °C to 8 °C to thaw or, alternatively, the frozen vials may also be thawed for 30 minutes at temperatures up to 25 °C for immediate use. Once thawed, the undiluted vaccine can be stored for up to 5 days at 2 °C to 8 °C, and up to 2 hours at temperatures up to 25 °C. The thawed vial must then come to room temperature and be gently inverted 10 times prior to dilution.
Some of the featured diagrams and instructions found in Reg 174
The complicated thawing and dilution process will obviously leave room for individual error. Healthcare practitioners are also warned not to shake the vials and instead to gently turn them 10 times. Prior to dilution, the vaccine should present as an off-white solution with no particulates visible. The guidance states that you must discard the vaccine if particulates or discolouration are present. The thawed vaccine must be diluted in its original vial with 1.8 mL sodium chloride 9 mg/mL (0.9%) solution for injection, using a 21 gauge or narrower needle and aseptic techniques and this complex, multistage process isn’t completed there.
The healthcare professional should then equalise vial pressure before removing the needle from the vial by withdrawing 1.8 mL of air into the empty diluent syringe. Then they should gently invert the diluted solution 10 times, again being careful not to shake the solution. The official guidance continues: “The diluted vials should be marked with the dilution date and time and stored between 2 °C to 25 °C. After dilution, the vial contains 5 doses of 0.3 mL.” The healthcare professionals are then told to “withdraw the required 0.3 mL dose of diluted vaccine using a sterile needle and syringe and discard any unused vaccine within 6 hours after dilution.”
The instructions must be followed precisely to safely administer the mRNA vaccine; there are no data available on potential consequences for the vaccine recipient if anything goes wrong during this tedious and complex multistage process. On 19 December 2020, video emerged of an official drive-thru vaccination hub which had begun operating out of a car park of Hyde Leisure Centre in Greater Manchester. The video in question, shared by No Comment TV on YouTube, shows people being vaccinated outdoors at Hyde Leisure Centre by gloveless staff and in less than sterile conditions. In an article in the Manchester Evening News four days prior to the videos release the local news site stated that “The first batch of the Pfizer/BioNTech vaccine arrives in the borough on Tuesday, with vaccinations starting at Hyde Leisure Centre on Wednesday, December 15.”
No Data Available (#5-10)
When reading Reg 174, you will soon notice a recurring theme throughout the document. The guidance clearly states on multiple occasions that there are no data available concerning some of the most important questions surrounding the mRNA vaccine. As previously noted, the actual Phase III section of the safety trials will not be completed until January 2023, meaning that two years of trials are still to be run before the vaccine can be confirmed as safe, effective and ethical.
5. The safety and efficacy of COVID-19 mRNA Vaccine BNT162b2 in children under 16 years of age have not yet been established
Although the guidance states that the safety and efficacy of the COVID-19 vaccine has not been established in children, it doesn’t mean that children have not been included within the studies. In fact, in the official Pfizer study entitled “Protocol C4591001”, one of the two main study groups included children as young as 12 years old. The inclusion of children in trials but not the guidance raises the important question, why were children included in the trial? If the vaccine is not to be given to those under the age of 16 years old, then why include children as young as 12 in the trials for an experimental vaccine technology never before authorised for use in humans?
The mainstream media, instead of raising concerns about the involvement of children in the Pfizer clinical trials, have been fully supportive of the move to test experimental pharmaceuticals on minors. CNN reported on children as young as 12 being involved in trials in an October 2020 article entitled “This 12-year-old is happy to be testing a Covid-19 vaccine” while Microsoft News recently announced that “China begins Covid test trials on children as young as age three.”
6. No data are available on the use of COVID-19 mRNA Vaccine BNT162b2 in persons that have previously received a full or partial vaccine series with another COVID-19 vaccine
We are currently witnessing the very first of many tailor-made vaccines being rolled out for general use, so don’t expect the COVID-19 jabs to be the only vaccines coming our way. With a 20 to 1 return on investment on many of these new technologies, most pharmaceutical giants will surely be lobbying governments across the globe for the next “necessary” vaccination program. The idea of multiple COVID-19 vaccinations throughout the year is already being presented as a very possible outcome for the future of humanity. Yet, no studies have been completed showing the risk of taking different types of vaccines. There have also been suggestions that people will have to have the same vaccine that they had previously taken every six months or so. This will leave Astrazeneca, Pfizer and Moderna picking up repeat vaccine contracts worth billions in secured future revenue before there are any real data on the results of the vaccines.
7. No interaction studies have been performed and there are no, or a limited amount of, data from the use of COVID-19 mRNA Vaccine BNT162b2
Admissions like these should be a cause for concern for anybody reading the official guidance. While officials and carefully chosen “trusted sources” are telling you that “no corners have been cut” in the race to approve these vaccines, it is also true that no full length studies have been completed either. These two facts are juxtaposed and obviously contradict the official narrative that is being thrust upon the general public by all of those involved.
It is clear that the officials have no real data on what will happen next and that there is a tsunami of ethical questions that are not being answered. In the absence of data, there will be speculation.
8. It is unknown whether COVID-19 mRNA Vaccine BNT162b2 is excreted in human milk and It is unknown whether COVID-19 mRNA Vaccine BNT162b2 has an impact on fertility
It is vital to note the potential dangers posed by the BNT162b2 to unborn and newborn babies as well as the reproductive organs in general. There are so many parts of the Pfizer/BioNTech clinical trials that have not yet been completed. Dr. Peter Klatsky, the Director of Fertility Preservation at the Bay Area’s Spring Fertility, talking about the coming animal trials which are to be performed over the coming months was quoted in SFGate as saying, “It will reassure me an awful lot if the protein expression is not seen on the placenta. That the mRNA isn’t making it to the placenta in animals,” he said. “I don’t expect to see any.” The article goes on to explain that it will be about another 9 months until the data has been collected and analyzed.
Section 4.6 of the official guidance recommends pregnant women should not recieve the BNT162b2 vaccine
Big names in mainstream media have also been caught recklessly promoting the vaccine to pregnant women, such as Karen Weintraub writing for USA Today, whose recent article quickly states, “Although there are very little data on how pregnant and nursing mothers will respond to a COVID-19 vaccine, professional organizations and individual doctors say the benefits are very likely to outweigh the risks.” Even though the clinical trials intentionally excluded pregnant women, Weintraub went on to state that “23 women in the Pfizer-BioNTech trial and 13 in Moderna’s became pregnant during the trial.”
While the UK’s official guidance is left sounding ambiguous, on the European continent, the European Medicines Agency (EMA) states that “the Pfizer vaccine should be considered on a case by case basis for pregnant women”, but they also reserve the right to alter the guidance if more data becomes available. It seems there is no longer any erring on the side of caution with some regulators when it comes to the COVID-19 vaccinations.
9. Non-clinical data reveal no special hazard for humans based on a conventional study of repeat dose toxicity but animal studies into potential toxicity to reproduction and development have not been completed
Animal studies have not been completed and, as referred to in the previous section, the data on those animal trials will not be available for another 9 months. It is, of course, a very rare decision to approve an experimental medical technology before any animal studies have been completed. This should be a great cause for concern for any free thinking man or woman. The fact that they have had to use what they refer to as “non-clinical” data in these studies is also in conflict with the idea that the trials were conducted to the highest professional standard. The document also fails to clearly define what non-clinical data actually means.
10. In the absence of compatibility studies, this medicinal product must not be mixed with other medicinal products
Possibly the most fascinating admission in the entire document is the absence of any compatibility studies when somebody is given the vaccine while on any other medication or medical treatment. The guidance clearly states “this medicinal product should not be mixed with other medical products.” This completely jaw dropping sentence will lead many to assume that if you are on any medication at all, then you shouldn’t be given the vaccine. Whether this refers to the mixing of other medical properties directly together with the vaccine, or simultaneous dosing of any other medical product is unclear from the official guidance.
The Mail Online and The Guardian reported in 2019 that a staggering 1 in 4 people in England – nearly 12 million people – were taking what was described as “addictive” prescription medicines such as antidepressants, sleeping pills and opioid painkillers, saying that “the NHS must take action”. Those statistics throw into question the mass rollout of a vaccination with no compatability studies. This makes the fact that elderly care home residents, followed by those aged over 80, will be the first to recieve the experimental Pfizer vaccine an extremely risky strategy. Also in 2019, Age UK reported that nearly 2 million older people were on more that 7 prescription medicines and were at “risk of side effects that are severe in some cases, and occasionally even life threatening.” This worrying issue has been barely reported by the “trusted news sources”.
A Conclusive Lack of Real Data
After examining the official guidance, one fact becomes glaringly obvious — there is little to no data on the official Pfizer vaccine in key areas. In the clinical trials, children as young as 12 years old were used as unnecessary guinea pigs. There also wasn’t enough care taken to avoid pregnant women being involved in the initial clinical trials and under the cover of unyielding and uneducated mainstream propaganda, the safety of some of the most vulnerable people involved in the vaccine trials have been ignored by Pfizer and the politicians who have successfully pushed for the public vaccination campaign to essentially replace mass clinical trials. The stage has been set for a potential disaster on an unimaginable scale. It isn’t only the participants of the trials who are risking their health for the sake of big pharmaceutical companies’ hyperinflated profit margin, but it is also the medical professionals who could be risking their futures by collaborating in these risky experimental trials, which will certainly see many people dead and irreversibly injured.
In one section of Reg 174, the Big Pharma giant lays out the risk to people’s health from the Pfizer/BioNTech vaccine. The most common adverse reaction in participants 16 years of age and older was pain at the injection site, which affected a massive 80% of those taking part in the Pfizer trials. Fatigue came a close second with 60% of trial participants becoming sluggish and tired. Half of those involved in the studies suffered from a headache as the experimental vaccine went to work while myalgia was experienced by 30% of vaccine recipients, though the results do not indicate whether the myalgia was acute (short-term) or chronic (long-term). Almost a third of participants came down with chills, while just under 1 in 5 people suffered from arthralgia (joint pain) and 1 in 10 from pyrexia (increased body temperature).
Adverse reactions reported in clinical trials are listed in the study in decreasing order of frequency and seriousness. Just under 1 in 10 people who take the vaccine will suffer from the very common and common adverse reactions referred to in the latter paragraph, such as headaches, myalgia and chills, but the more serious issues are classified as uncommon – including Lymphadenopathy (which causes swollen or enlarged lymph nodes) and nervous system disorders – which may affect up to 1 in 100 people. Rare adverse reactions that could affect up to 1 in 1000 people and very rare adverse reactions that would affect less than 1 in 10,000 of the vaccine recipients were not included in Pfizer’s self-reported safety information. It has obviously been decided that this information should be kept out of the public domain as much as possible to avoid any further vaccine hesitancy.
Not only does the official guidance actively hide the types of rare and very rare adverse effects, but they have also been leaving out some of the adverse reactions reported during the clinical trials. As I write this, the Reg 174 guidance for healthcare professionals is on version 10.1 of the document and, since its release, they have yet to admit to the potential of a certain uncommon adverse reaction to the vaccine being a specific nervous system disorder. Structural nervous system disorders include brain or spinal cord injury, Bell’s palsy, cervical spondylosis, carpal tunnel syndrome, brain or spinal cord tumors, peripheral neuropathy, and Guillain-Barré syndrome. However, previous versions of the guidance gives no clue as to what type of nervous system disorders they were referring to. However, recent articles in the USA Today, heavily promoted by the Microsoft Network, suggested that the Bell’s palsy some people came down with in the vaccine trials wasn’t related to the Pfizer jab. The article states that on Dec. 10, the FDA’s Center for Biologics Evaluation and Research held the 162nd meeting of the Vaccines and Related Biological Products Advisory Committee to discuss the emergency use authorization of the Pfizer-BioNTech COVID-19 vaccine. The USA Today piece even goes on to admit that , “a 53-page briefing noted that there had been four cases of Bell’s palsy among the vaccinated group and none among the placebo group.”
Bell’s palsy causes drooping facial muscles similar to the effects of a stroke, image source PTHealth.com
Even though Miriam Fauzia, who wrote the USA Today piece, claims that the Bell’s palsy was not related to the experimental Pfizer vaccine, the 53-page briefing she sources clearly states, “Among non-serious unsolicited adverse events, there was a numerical imbalance of four cases of Bell’s palsy in the vaccine group compared with no cases in the placebo group, though the four cases in the vaccine group do not represent a frequency above that expected in the general population.” While it is true that 1 to 4 people in 10,000 will develop Bell’s palsy within the general population, it should be noted that the 4 cases in the vaccine trials and none in the placebo group makes for a statistical anomoly that must be examined more thoroughly. Instead, the mainstream media moved quickly to discredit the Bell’s palsy links to the Pfizer vaccine using various misleading tactics to achieve their aims.
Many mainstream outlets were caught spouting the same misleading information with articles entitled “Why you shouldn’t worry about a connection between Bell’s palsy and COVID-19 vaccines,” from Business Insider and a Reuters article from 14 December 2020 entitled, “Fact check: Photo does not show three recipients of Pfizer’s COVID-19 vaccine that developed Bell’s palsy.”
In the case of the Reuters article, which is described as written by “Reuters Staff” rather than a specific journalist, the focus was not on the four Pfizer clinical trial participants who developed Bell’s palsy but instead the article discredits a random post on social media of three people with Bell’s palsy unconnected to the Pfizer vaccine. These type of misinforming mainstream media articles are commonly found to be using obvious fallacies to mislead their readership and with no individual taking responsibility for writing the misinforming piece, a trick repeated by many other media companies complicit with the official narrative. The Reuters article even goes on to admit that: “According to the FDA’s briefing document dated December 10, Bell’s palsy was reported in four vaccine participants and none in the placebo group, out of the 44,000 total participants of the late-stage vaccine trial.” However, the title of the Reuters article would mislead even some of the most keen eyed observers.
The mainstream media has been creating a flood of misleading stories, but it appears as though they have been given carte blanche to continue to do so, probably because they are sticking so tightly to the official narrative. It’s a narrative that is thick with irony, for it is the “trusted sources” who are being caught systematically misleading the general population again and again while also declaring a propaganda war against “fake news”.
The official guidance noted in Reg 174 doesn’t only highlight the serious lack of real data gained from Pfizer’s clinical trials for its Covid-19 vaccine so far, but it also exposes the wealthy medical professionals involved in these experimental vaccine development programs as complacent, reckless and very naive. It’s no secret that children are, more often than not, incapable of giving informed legal consent for such a risky and unethical enterprise. But the pro-vax extremists are using every tactic to coerce and manipulate children and their guardians into becoming human guinea pigs for Big Pharma. Pregnant women are also treated as acceptable collateral damage to advance the new science of gene, mRNA and DNA manipulation, a science and technology that pushes a sinister transhumanist agenda.
Don’t be fooled by the carefully worded vacuous celebrities, self-serving politicians, Big Pharma, and the mainstream medias authoritarian style misinformation campaigns. Keep your humanity intact and read their own words. The government guidance to healthcare professionals clearly states on multiple occasions that there are “no data available”.
Johnny Vedmore is a completely independent investigative journalist and musician from Cardiff, Wales. His work aims to expose the powerful people who are overlooked by other journalists and bring new information to his readers. If you require help, or have a tip for Johnny, then get in touch via johnnyvedmore.com or by reaching out to johnnyvedmore@gmail.com
Emergency Hospitals Dismantled Despite Claim Hospitalisations Worse Than ‘First Wave’
The hospitals have been almost completely empty for the duration of the health crisis
By Steve Watson | Summit News | December 29, 2020
A report has confirmed that emergency hospitals in the UK are being dismantled and removed, despite government claims that hospitalisations from coronavirus have hit a level HIGHER than they were during the first wave of the pandemic back in March and April.
The reports in the Daily Mail and the London Telegraph note that the facilities, known as ‘Nightingale hospitals’, set up at huge conference centres and other warehouse spaces are “being quietly taken apart” because there are not enough staff to run them.
Despite the seven facilities throughout the UK costing as much as £220million to set up and equip, the hospitals have been almost completely empty for the duration of the health crisis.
Indeed, just 57 Covid-19 patients were admitted to NHS Nightingale London between April and the start of May, according to Department of Health records. The facility was then put back into ‘standby’, and left empty.
The report states that the ExCeL Centre, which hosts the London facility, has confirmed that 90 per cent of the hospital has already been removed, including stripping 4000 beds and hundreds of additional of ventilators.
Videos of the facilities being dismantled first surfaced in the Summer:
The government has repeatedly pushed the narrative that the lockdowns have been necessary to ‘protect the NHS’, yet now it is taking apart the hospitals it says were set up to alleviate the strain.
It has been claimed that a third of major hospital trusts in England are now experiencing more Covid-19 patients than at the peak of the first wave. In the East and South West, more than half of all hospitals say they have more patients now than earlier in the year.
National Health Service data claims that over 20,000 beds are now occupied by COVID patients, up from 17,700 recorded last week, and surpassing the almost 19,000 recorded in mid April.
Throughout the crisis, we have been told that hospitals are on the brink of being overwhelmed, yet reports have continued to emerge suggesting that hospitals are up to four times emptier than usual.
Despite the claims that there are not enough NHS staff to man the facilities, there has been a resurgence of nurses posting dancing tik-tok videos:
Biden’s Pony Problem: Why The Hunter Biden Scandal Is No Dead Horse
By Jonathan Turley | December 23, 2020
President-elect Joe Biden has a pony problem. During the primary, Joe Biden bizarrely responded to a woman who asked why voters should believe that he could win a national election by saying “You’re a lying dog-faced pony soldier.” That encounter came to mind when Biden this week mocked Fox reporter Peter Doocy, who violated the virtual news blackout on the Hunter Biden story by asking about the scandal. Biden immediately walked off stage and then stopped and said “Yes, yes, yes. God love you, man — you’re a one-horse pony, I tell you.”
Like many kids this Christmas, many voters are still angling for a pony. Biden has spent months mocking the Hunter Biden story – and anyone asking about it. When CBS News reporter Bo Erickson asked Biden about his son’s scandal, Bo Erickson drew a similar rebuke from Biden. He simply asked ‘Mr. Biden, what is your response to the New York Post story about your son, sir?’ Biden’s response was again a personal attack: “I know you’d ask it. I have no response, it’s another smear campaign, right up your alley, those are the questions you always ask.” Biden also blew up at a question that referred by the scandal by a NBC reporter and at a Fox reporter who asked about his son.
It is just not working. The media openly worked to bury the Hunter Biden scandal before the election, but the ponies keep finding their way back. The problem is when you have one reporter like Doocy who refuses to be corralled and insists on an answer to a serious question.
The question yesterday was a good one. Doocy yelled out “Mr. President-elect, do you still think that the stories from the fall about your son Hunter were Russian disinformation and a smear campaign like you said?” Biden’s response of “yes, yes, yes” seemed to continue a discredited claim (indeed, “disinformation”) put out by figures like House Intelligence Committee Chairman Adam Schiff who assured the pubic that the allegations against “this whole smear on Joe Biden comes from the Kremlin.” Some 50 former intelligence officials, including Obama’s CIA directors John Brennan and Leon Panetta, also insisted the laptop story was likely the work of Russian intelligence. Cable hosts and journalists laughed at the laptop story as fake news to justify the blackout on coverage before the election.
Then the pony showed up again. After the election, it was confirmed (as some of us discussed in columns before the election) that Hunter Biden is under federal investigation. The laptop appears to be genuine. The emails appear to be genuine. And Doocy continued to ask the obvious questions.
Biden is still hoping that he can continue to mock and the media will continue to do the rest. One reporter yesterday did raise the scandal but only to ask if Biden discussed it with Attorney General candidates (the campaign already said that Biden was going to allow the Justice Department to reach its own conclusions). There are other obvious questions, including whether a key business associate of the Bidens, Anthony Bobulinski, is lying. Either Tony Bobulinski or Joe Biden is lying. Bobulinski is repeatedly praised by Hunter Biden in the emails and identified as the person in control of transactions for “the family.” He has directly contradicted Joe Biden’s denial of any knowledge or involvement in his son’s dubious dealings.
There is a reason why Biden may not want to answer that question. If he calls Bobulinski a liar, Biden would be hit with a defamation lawsuit within days. He would then be forced to go under oath. Such depositions present their own dangers. Just ask Bill Clinton. So it is not a pesky pony but a sworn deposition that Biden may be trying to avoid.
The same problem exists on other questions. For example, not only were Joe and Jill Biden included as “office mates” with controversial Chinese investor (and associate of Hunter) Gongwen Dong, but emails also refer to unsecured loans going to the Biden family and shares going to “the big guy.” The “big guy” appears to be Joe Biden. Moreover, Biden spent the election denying that his son did anything wrong and that he made no money from China. The question is when Biden learned of the federal investigation and whether he was aware of the dealings over multimillion dollar unsecured loans (as well as alleged gifts like a valuable diamond givento his son). Answering those questions falsely could trigger a congressional investigation and then more ponies would show up.
That is the problem with a bunker press strategy of denial and isolation. Like water, truth has a way of coming out. Clearly many in the media will continue to be in the bag for Biden. However, horses tend to gather where the water is found. First, there was one pony (Doocy). Then another showed up (Erickson). Before you know it, you have a herd and a threat of a stampede. Then it could be too late.
In the mocking comment to Doocy, Biden was clearly trying to say a “one-trick pony.” That trick however was once called “journalism” back in the day when reporters doggedly demanded answers, particularly on questions like influence peddling. So many of us still hoping for ponies – and even some answers – for Christmas.
New York Can’t Buy Its Way Out Of Blackouts
By David Wojick, Ph.D. ~ PA Pundits ~ December 26, 2020
New York City will soon be home to the world’s biggest utility-scale battery system, designed to back up its growing reliance on intermittent renewables. At 400 MWh this batch of batteries will be more than triple the 129 MWh world leader in Australia.
The City of New York’s director of sustainability (I am not making this title up), Mark Chambers, is ecstatic, bragging: “Expanding battery storage is a critical part of how we advance momentum to confront the climate emergency while meeting the energy needs of all New Yorkers. Today’s announcement demonstrates how we can deliver this need at significant scale.” (Emphasis added)
In reality the scale here is incredibly insignificant.
In the same nonsensical way, Tim Cawley, the president of Con Edison, New York’s power utility, gushes thus: “Utility scale battery storage will play a vital role in New York’s clean energy future, especially in New York City where it will help to maximize the benefit of the wind power being developed offshore.”
This puts the Con in Con Edison.
Here is the reality when it comes to the scale needed to reliably back up intermittent renewables. For simplicity let us suppose New York City is 100% wind powered. Including solar in the generating mix makes it more complicated but does not change the unhappy outcome very much.
NYC presently peaks at around 32,000 MW needed to keep the lights on. If Mr. Biden makes all the cars and trucks electric it might be closer to 50,000 MW but let’s stick to reality.
This peak occurs during summer heat waves which are caused by stagnant high pressure systems called Bermuda highs. These highs often last for a week and because they are stagnant there is no wind power generation. Wind turbines require something like sustained winds of 10 mph to move the blades and more like a whistling 30 mph to generate full power. During a Bermuda high folks are happy to get the occasional 5 mph breeze. These huge highs cover many states so it is not like we can get the juice from next door.
So for reliability we need, say, seven days of backup, which is 168 hours. Here’s the math:
32,000 MW x 168 hours = 5,376,000 MWh of stored juice needed to just make it. Mind you for normal reliability we usually add 20% or so. Did I mention electric cars?
It is easy to see that a trivial 400 MWh is not “significant scale.” It is infinitesimal scale. Nothing. Nada. Might as well not exist.
More specifically, 5,376,000 divided by 400 = 13,440 so only 13,439 more to go.
On the other hand, this measly 400 MWh battery array may well cost half a billion dollars, which is significant, especially to the New Yorkers who will pay for it. No cost figures are given because the system is privately owned, but EIA reports that the average utility scale battery system runs around $1.5 million a MWh of storage capacity. That works out to $600 million for this insignificant toy.
So what would it cost to reliably back up wind power, at this MWh cost and NYC’s scale? Just over $8,000,000,000,000 or EIGHT TRILLION DOLLARS. I have not seen this stupendous sum mentioned in the media. Perhaps Con Ed has not mentioned it.
Then too, New York State has the same problem. Only much bigger if New York City is included, which it often is.
But hey, maybe the cost will come down a few trillion. Not if we create a seller’s market by rushing into intermittent renewables, which is certainly where we are headed. After all, this is just New York City. Imagine what backing up America with batteries might cost. Don’t bother because it is impossible.
I should also add that we have no idea how to make 5 million MWh of batteries work together. The tiny 400 will be a challenge. It may not be possible.
Maybe fracked geothermal, the reliable renewable, is the answer. Or how about coal, oil, gas and nuclear power? Too bad they are all out of fashion.
All of this battery backup hype is a scam, and not just in New York either. The papers are full of this con, from coast to coast. The utilities know perfectly well that these loudly touted battery buys are a hoax, but they are getting rich building the wind and solar systems the politicians are calling for.
The voters are oblivious to these impossible numbers, since they are told that intermittent wind and solar are cheaper than reliable coal, gas and nuclear. Only when the sun shines bright and the wind blows hard, which is not all that often.
Reality is just sitting there, waiting. It can’t work so it won’t work. At this point it is just a question of how and when we find out the hard way.
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Anti-science
The infinite list
The Naked Emperor’s Newsletter | October 12, 2022
Almost three years ago science entered a new dark age.
Jay Bhattacharya, a professor of medicine at Stanford University and co-author of the Great Barrington Declaration, seems to agree. He has been compiling a list of the examples of anti-science we have unfortunately become used to.
I have listed his thoughts so far but the list is continually expanding... continue
Blog Roll
Aletho News- Iran War Confusion & Mixed Messaging /Lt Col Daniel Davis
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- An All-American Retort to Israel’s Invasion of Lebanon
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- No Tricks Zone
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- European Institute For Climate And Energy: “Climate Debate is Seldom About Science”
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