Brownstone Institute
The Vaccine Was “95% Effective” How?
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From the Brownstone Institute
BY
The 1840 Treaty of Waitangi between the British Crown and Maori chiefs was a landmark event in the history of New Zealand. Drafted in English, a Maori translation was prepared, ostensibly to ensure that Maori could have an accurate understanding of the terms. In retrospect, it is less clear that a meeting of the minds was intended:
The English and Māori texts differ. As some words in the English treaty did not translate directly into the written Māori language of the time, the Māori text is not a literal translation of the English text. It has been claimed that Henry Williams, the missionary entrusted with translating the treaty from English, was fluent in Māori and that far from being a poor translator he had in fact carefully crafted both versions to make each palatable to both parties without either noticing inherent contradictions.
“The covid vaccine is 95% effective” is a contemporary Treaty of Waitangi. The original is in the language of clinical trials. It was never translated. The public interpreted this phrase in their native language, normal English. What Pfizer said and what the public heard were quite different. The public would have been far more skeptical of these products had the clinical trial results been translated into normal English.
What we need is a proper translation and an explanation of how miscommunication happened.
The Injections Did Not Stop Infection
By now, everyone knows that the Pfizer and Moderna products did not stop people from getting Covid. Covid disease has mowed a wide strip through the double and triple-masked talking heads who told everyone that the shots would make them immune.
What is less well known is that:
- The products were never expected to stop infection or transmission.
- The clinical trials did not test for their ability to do so.
A clinical trial is designed to test a drug for effectiveness, which is strictly defined by one or more endpoints. An endpoint is a measurable outcome that can be assessed for each participant. With that in mind, prevention of infection was not an endpoint of the BioNTech/Pfizer injection clinical trials. And, this was known in 2020 before the products were approved for emergency use and distributed to the public starting in 2021.
In this New England Journal of Medicine research summary, Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine, under Limitations and Remaining Questions, we find that “whether the vaccine protects against asymptomatic infection and transmission to unvaccinated persons” remains unanswered by the clinical trial.
What did the clinical trial test for, if not the ability of the mRNA vaccine to stop transmission and/or infection? The trial was designed to test the ability of the injections to prevent “symptomatic Covid 19 cases” defined as one or more of a number symptoms and a positive test (see page 7 of the supplementary appendix for details).
@pfizer tweeted in Jan 2021 that stopping transmission was their “highest priority”. Their product does not do that, nor did the tweet make a claim that it did so. But it was their highest priority nonetheless. That, and getting as many people injected as possible.
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Failure to Prevent Infection Was Known Before the Rollout
In October 2022, a Pfizer executive testified to an EU body that Pfizer had not tested the ability of the vaccine to stop transmission. This story was shocking to some and generated accusations that Pfizer had lied about the capabilities of the shots. But this information had been available since the trial results were released early in 2021. Pfizer had already been criticized for this.
Dr William A Haseltine PhD, wrote in Forbes in September 2020:
What would a normal vaccine trial look like?
One of the more immediate questions a trial needs to answer is whether a vaccine prevents infection. If someone takes this vaccine, are they far less likely to become infected with the virus? These trials all clearly focus on eliminating symptoms of Covid-19, and not infections themselves. Asymptomatic infection is listed as a secondary objective in these trials when they should be of critical importance.
On October 21, 2020 the editor of the BMJ (British Medical Journal) Peter Doshi asked:
Will covid-19 vaccines save lives? Current trials aren’t designed to tell us
Peter Hotez, dean of the National School of Tropical Medicine at Baylor College of Medicine in Houston, said, “Ideally, you want an antiviral vaccine to do two things . . . first, reduce the likelihood you will get severely ill and go to the hospital, and two, prevent infection and therefore interrupt disease transmission.”
Yet the current phase III trials are not actually set up to prove either. None of the trials currently underway are designed to detect a reduction in any serious outcome such as hospital admissions, use of intensive care, or deaths. Nor are the vaccines being studied to determine whether they can interrupt transmission of the virus….
Is It Even a Vaccine?
A vaccine that prevents infection is known as “neutralizing” or “sterilizing”. I am a software engineer with no training in medicine, pharmacology or clinical trials. I consider myself a good barometer of what the average untrained person would think about such things. Prior to 2021 I had thought that immunity was a necessary condition for a drug to earn the title of “vaccine”. If anyone had asked me, I would have told them that the Covid injections were a treatment, not a vaccine.
The Wikipedia article about vaccines (Mar 5 2023) aligns with my untrained understanding:
A vaccine is a biological preparation that provides active acquired immunity to a particular infectious or malignant disease. … A vaccine typically contains an agent that resembles a disease-causing microorganism and is often made from weakened or killed forms of the microbe, its toxins, or one of its surface proteins. The agent stimulates the body’s immune system to recognize the agent as a threat, destroy it, and to further recognize and destroy any of the microorganisms associated with that agent that it may encounter in the future.
Cornell Law provides the following legal definition of vaccine, sourcing 26 USC § 4132(a)(2), which is consistent with the above:
The term “vaccine” means any substance designed to be administered to a human being for the prevention of 1 or more diseases.
The definition published by the CDC prior to 2021 said much the same. But the CDC website changed the definition on or after August 2021. The older version found on the internet archive is here (emphasis added):
Immunity: Protection from an infectious disease. If you are immune to a disease, you can be exposed to it without becoming infected.
Vaccine: A product that stimulates a person’s immune system to produce immunity to a specific disease, protecting the person from that disease.
Here is the new version (emphasis added):
Vaccine: A preparation that is used to stimulate the body’s immune response against diseases.
The earlier pair of definitions is quite easy to understand. The latter, much more difficult. What exactly is a “preparation”? Does a vaccine stimulate the body or only prepare the body? What is or is not a vaccine according to the new definition?
While the CDC may think that they can change the meanings of words whenever they like, public memory retains the original meaning. The assumption of immunity permeates almost all non-expert level discussion of vaccines. A web search for “why are vaccines good” shows results that assume or imply immunity.
Even the CDC did not finish the job of memory-holing the old language. On the very same CDC website, under 5 Reasons It Is Important for Adults to Get Vaccinated, we read “By getting vaccinated, you can protect yourself and also avoid spreading preventable diseases to other people in your community.” And then, “Vaccines Can Prevent Serious Illness”.
The timing of the CDC’s edit suggests to me that prior to 2021, the CDC had the same understanding of vaccines as I do. I believe that they wanted a new definition because they knew that the products being developed at warp speed were not vaccines in the original sense of the word. And it was important that those products be called “vaccines” for reasons that I will explain later. This incident brings to mind a meme that I no longer have a link to. captioned: “We changed what ‘definition’ means so you can’t say that we redefined anything.”
What Does “95% Effective” Mean?
The “95% effective” message was repeated in nearly all reporting on the clinical trials. But the question, “effective at doing what?” was rarely asked. To answer this requires walking down the links of a chain of terminology from the world of clinical trials.
The first link in the chain is “risk”. Risk is the probability of a bad outcome. These are assumed to happen randomly within a group. A clinical trial must define in advance the bad outcomes that the drug intends to avoid. The next link is “endpoint”. Each distinct bad outcome is an “endpoint”. The trial compares the endpoints between a control group who did not take the drug and a test group, who did.
The purpose of a clinical trial is to determine the ability of a drug to reduce risk. A drug that reduces risk is “effective”. There are two ways of quantifying risk reduction. From the NIH glossary:
Absolute risk reduction (ARR) or risk difference
the difference in the incidence of poor outcomes between the intervention group of a study and the control group. For example, if 20 per cent of people die in the intervention group and 30 per cent in the control group, the ARR is 10 per cent (30–20 per cent).
Relative risk (RR)
the rate (risk) of poor outcomes in the intervention group divided by the rate of poor outcomes in the control group. For example, if the rate of poor outcomes is 20 per cent in the intervention group and 30 per cent in the control group, the relative risk is 0.67 (20 per cent divided by 30 per cent).
The difference between the ARR and RR (also known as “RRR”, to align with ARR) is in the denominator. The ARR divides by the number of participants in one of the groups. The RRR divides by the number of people with bad outcomes in the control group – a necessarily much smaller number.
The ARR is the number most relevant for a drug – such as the Pfizer injections – that was to be given to everyone. But the RRR is the preferred method of presentation for pharma when they want to exaggerate the effectiveness of a drug because it will always be a much larger number. Would you take a drug that could reduce the incidence of a rare disease by 50%? From 10 per 1 million to 5 per 1 million is an 50% RRR and an 0.0005% ARR.
The 95% figure cited for the covid injections is the relative risk. The absolute risk reduction was 0.84%. In a slide deck from the Canadian Covid Care Alliance(CCCA), slide 11 shows how the 91% was achieved (it is 91%, not 95%, because the it refers to an earlier version of the study):
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The research paper COVID-19 vaccine efficacy and effectiveness—the elephant (not) in the room puts the ARR in the 1% range. The CCCA slide deck gives an ARR of 0.84%, though it is not clear how they reached this number, based on the other numbers in their slides.
A clinical trial finding of a 1% ARR means that 99% of the people who take the drug either did not experience the condition that the drug treats, or they did experience it, but were not helped by the drug. The 1% both had the condition and were helped by the drug. Another way of saying this is the Number Needed to Treat (NNT). NNT is the reciprocal of the ARR and is the number of people who must take the drug to help one person reach the endpoint. An ARR of 1% corresponds to an NNT of 100 people.
We can now answer the question of the meaning of vaccine effectiveness. The endpoint of the trial was a severe confirmed case of covid at least 7 days after the second dose. This endpoint requires the participant in the trial to have covid symptoms and a positive covid test. “95% effective” means that 95% of the patients who had Covid symptoms and a positive test were in the control group. Five percent were in the test group.
Here’s what “95% effective” did not mean: if you take the shots, then you will have a 95% lower chance of getting covid. But that is how most people understood it because that is what the words mean in normal English.
Then the Lying Started
Once the public had their hopes raised by the false translation of the “95% effective” message, the pandemic-industrial-complex went into high gear to amplify it. They stated the incorrect message loudly, frequently, and as if it were fact. The injections would – with 100% certainty (perhaps 200%) – protect you from infection. Many of the people who said this were doctors or scientific researchers who must have understood how to interpret clinical trials.
Here are some choice quotes that did not age well:
- “You’re not going to get Covid if you have these vaccinations.” Joe Biden, CNN Town Hall July 2021
- “Now we know that the vaccines work well enough that the virus stops with every vaccinated person. A vaccinated person gets exposed to the virus, the virus does not infect them, the virus cannot then use that person to go anywhere else,” she added with a shrug. “It cannot use a vaccinated person as a host to go get more people. [Vaccines] will get us to the end of this.” – Rachel Maddow, March 2021
- “When people are vaccinated they can feel safe that they won’t get infected, whether they’re outdoors or indoors.” – Dr. Anthony Fauci, May 2021(outdoors: seriously?)
- “Vaccination against COVID-19 prevents breakthrough infections, Stanford researchers find.” – Stanford Medicine, July 2021
- Vaccinated people become “dead ends” for the virus – Anthony Fauci, May 2021
Demonizing the Unvaxxed
The public has consistently over-estimated the infection fatality rate of Covid. Some even believed the fatality rate to be above 10%. They believed that we were in great danger. They also believed that the “95% effective” vaccine would bring the pandemic to a quick end, once everyone had taken it. Anyone who refused to do so was therefore risking not only their own life, but everybody else’s as well.
Dr Anthony Fauci estimated herd immunity would emerge when around 60% of the population had taken the vaccine … or perhaps 70, 80, no wait … 85%. Or maybe 100% (which would include large numbers who already had natural immunity). Bill Gates extended that to everyone on earth.
The narrative then turned to demonization of those who refused to submit to vaccine coercion. The selfish anti-social behavior of the anti-vaxxers with their stubborn attachment to “free dumb” that was keeping everyone locked indoors and forcing us all to wear diapers on our faces. Yale University behavioral researchers tested messaging strategies to determine whether shame, embarrassment or fear was most effective.
President Biden said that we the nation was experiencing a “pandemic of the unvaccinated”. Later, Biden ominoulsy warned the unvaccinated that he had been waiting a long time for them to get injected, but “our patience is wearing thin”. In December of 2021 the White House issued a cheery year end greeting to the vaccinated. The unvaccinated, on the other hand, were “looking at a winter of severe illness and death.” Merry Christmas.
Even South Park, which I consider a reliable source of contrarian political opinion, ran a storyline set in the year 2050 in which every single character had to be vaccinated for the 30-year pandemic to end. This episode featured one lone holdout who would not get vaccinated due to a crustacean allergy i.e. for “shellfish reasons”. This gag took aim at people who considered the vaccine to be a violation of body autonomy, and those who objected to components used in its development for religious reasons, thereby scoring a “two for one”.
Volumes can, and will, be written about the intense onslaught of propaganda aimed at getting two needles in every deltoid. I will provide one more example that represents no more than the median level of insanity; plenty of people called for the same or worse. @ClayTravis, in February 2023, tweeted the results of a Rasmussen poll from 2022:
Last January 60% of Democrats wanted to lock everyone who didn’t get the covid shot in their houses. Over 40% of Democrats wanted those who rejected the covid shot sent to quarantine camps. Over 40% also wanted anyone who criticized the covid shot fined & imprisoned. Over a quarter wanted those who didn’t get the covid shot to have their kids seized.
While there were many agendas driving the madness, the Treaty of Waitangi effect was a critical part in carrying it out. If the message had been that “everyone is going to get exposed to covid – injected or not”, then it could not have happened. The misunderstanding convinced the public that mass vaccination would stop the pandemic; and that the holdouts were prolonging it. Without this belief, none of the coercion made any sense: employment mandates, school mandates, quarantine camps, or vaccine passports. As the hysteria fades, the last remaining mandates are being dropped as the reality sinks in that the shots do not stop the spread.
Welcome to Waitangi World. I hope that you have a pleasant stay.
Brownstone Institute
The Latest “Bird Flu” Psyop
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From Brownstone Institute
By
I am expert in influenza, and have consulted with the WHO over the past two decades on the topic of flu vaccines. This is one subject matter I am extremely knowledgeable about. This goes back to my medical school days, when I worked with Robert Lamb, one of the top influenza virus specialists in the world. It extended through much of my career, including my serving as Director of Clinical Influenza Vaccine Research for Solvay Biologicals, in which I oversaw over $200 million in federal (BARDA) alternative (cell-based) influenza vaccine research funding.
What is happening now with “Bird flu” is another psyops campaign being conducted by the administrative/deep state, apparently in partnership with Pharma, against the American people. They know and we know that the “vaccines” being produced will be somewhat ineffective, as all flu “vaccines” are. The government is chasing a rapidly evolving RNA virus with a syringe, just like they did with HIV and Covid-19.
Generally, the currently circulating avian influenza strain in the US does not include any cases of human-to-human transmission. And the current mortality, with over 60 cases identified, is 0%. NOT 50%.
All the while they are getting prepared to roll out masks, lockdowns, quarantines, etc.
All the while getting ready to roll out mRNA vaccines for poultry and livestock, as well as for all of us.
The more they test, the more “Bird flu” (H5N1) they will find. This “pandemic” is nothing more than an artifact of their newly developed protocols to test cattle, poultry, pets, people, and wildlife on a massive scale for avian influenza. In years past, this was not even considered. In the past, the USG did fund a massive testing and surveillance program called “Biowatch.” That program was a colossal failure and a massive waste of money. Billions of dollars.
Of course, these facilities producing the tests have been repurposed from the Covid-19 testing facilities.
Key questions include:
Will we all comply?
Will we be forced to comply?
Will President Trump go along with the PsyWar/psyops campaign again?
We will know soon enough.
As the United States is testing everyone who has even the mildest symptoms for the H5N1 (avian) influenza, guess what – they are finding it! This is what we call in the lab, a “sampling bias.”
Globally, from 1997 until the present, there have been 907 reported cases of H5N1. And in fact, this particular outbreak was not the worst – and it is the only one where a massive testing campaign has occurred. It appears that this is partly due to the new diagnostic capabilities developed and deployed during Covid-19. The more you test, the more you find. But is it clinically significant?
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The Case Study of Tetanus: Supply Chain Issues.
The CDC recommends a booster for the tetanus vaccine every 10 years for adults.
However, research published almost a decade ago suggests that the protection from tetanus and diphtheria vaccination lasts at least 30 years after completing the standard childhood vaccination series.
“We have always been told to get a tetanus shot every 10 years, but actually, there is very little data to prove or disprove that timeline. When we looked at the levels of immunity among 546 adults, we realized that antibody titers against tetanus and diphtheria lasted much longer then previously believed.”
-Mark K. Slifka, Ph.D, study author
This research, published in a highly reputable journal, suggests that a revised vaccination schedule with boosters occurring at ages 30 and 60 would be sufficient. As this was published in early 2016, the US government, at the very least, could have commissioned easily designed prospective and retrospective studies to confirm these results. And those results would have been published by now, with the tetanus adult schedule revised to reflect what is now known about the durable immunity of tetanus and diphtheria vaccines. Reducing the boosters to just two shots would save the government vast sums of money.
Not only that, but both the tetanus and diphtheria vaccines carry risks for adults. It is estimated that 50%–85% of patients experience injection site pain or tenderness, 25%–30% experience edema and erythema. Higher preexisting anti-tetanus antibody levels are also associated with a higher reactogenicity rate and greater severity (reference).
Anaphylaxis after tetanus vaccination represents a rare but potentially serious adverse event, with an incidence of 1.6 cases per million doses. That means if 100 million adults receive the booster every ten years, 320 cases of anaphylaxis will be avoided over the 30-year period – from those two boosters being eliminated. Tetanus has always been a “rare” disease, spread through a skin wound contaminated by Clostridium tetani bacteria, commonly found in soil, dust, and manure. Before vaccines were available, there were about 500 cases a year, with most resulting in death. Concerns about vaccine-associated adverse events when immunizations were performed at short intervals led to a revision of the tetanus/diphtheria vaccination schedule in 1966 to once every 10 years for patients >6 years of age.
It has recently come to my attention that the traditional stand-alone tetanus vaccine (TT) that one used to receive as an adult has been discontinued due to WHO recommendations. Their reasoning being:
Use of TTCV combinations with diphtheria toxoid are strongly encouraged and single-antigen vaccines should be discontinued whenever feasible to help maintain both high diphtheria and high tetanus immunity throughout the life course.
The CDC blames the shuttering of the only plant producing TT for the current lack of a stand-alone TT vaccine.
Now, in order to get a booster tetanus shot, an adult must take the following.
- Td: Sanofi’s Tenivac protects against tetanus and diphtheria. Given to people 7 years and older as a booster every 10 years. *A version also includes pertussis (eg DPT), but due to the risk of encephalitis, it is not recommended as a booster.
Why is the DPT combination vaccine discouraged in adults due to encephalitis risk, but is it recommended for children? Another one of those inconvenient issues that plague the CDC-recommended childhood vaccine schedule.
While supplies of diphtheria, tetanus, and pertussis (Tdap) vaccines (Sanofi’s Adacel and GSK’s Boostrix) aren’t limited, they are more expensive, and a very small fraction of patients can develop encephalopathy (brain damage) from the pertussis component.
In the United States, diphtheria is virtually non-existent, with only 14 cases reported between 1996 and 2018. Of those cases reported, most were from international travelers or immigrants.
The market for a stand-alone TT vaccine vanished worldwide due to WHO recommendations to stop the sales of the TT vaccine. Which was due to the relatively few, economically stressed countries where diphtheria is still an issue. So, therefore, the only facility manufacturing the TT vaccine was shut down within the last year.
The blowback from the WHO recommendations is that now there is a shortage of tetanus and diphtheria (Td) vaccine in the United States, according to the Centers for Disease Control and Prevention (CDC) website.
This all comes down to poor planning. And illustrates why supply chain issues and infectious disease countermeasure stockpiles are essential considerations for governments.
The good news is that unless one is immunosuppressed, most of us have almost lifelong immunity against tetanus and diphtheria.
My recommendation is that unless one gets a very deep and dirty puncture wound and has not had a tetanus shot in over ten years or longer, avoid that booster.
Here is the ugly secret about influenza vaccines. They are given to protect one group of vulnerable people. Those who are immunosuppressed, and that cohort includes the very elderly.
If those influenza vaccine manufacturing plants only make enough vaccines for those susceptible to a severe case of the flu, there would not be enough of a market to sustain their production costs. Furthermore, if there were a pandemic of some sort of highly pathogenic influenza, there would not be sufficient capacity to make enough vaccines to meet demand.
Egg-based influenza vaccine production requires super “clean” eggs; about 100 million “clean” fertilized eggs are needed annually for vaccine production in the US alone. Candidate vaccine viruses are injected into the eggs. If the process is shuttered, the whole production comes to a screeching halt. Many vaccines can be stored for long periods. Even as long as a decade. This stockpiling system works well for DNA viruses with a low mutation rate. Stockpiling is rarely a solution for vaccines developed for RNA viruses that mutate rapidly.
Therefore, the influenza vaccine is pushed on the American people year after year. As a way to maintain “warm base manufacturing” and ensure sufficient market size to support industrial operations.
I have spoken on this subject at the WHO and US government agencies, as well as many, many conferences. Unfortunately, because the mRNA and RNA vaccine platforms require a lot of freezer space (commonly -20°C) to stockpile for even short periods, this limits the ability to stockpile. Furthermore, the frozen storage requirements are only for up to 6 months. That means stockpiling for more extended storage is not currently done, and it is back to square one on the supply chain issue.
The issue with freezer space and mRNA vaccines is one that most likely won’t be solved. This benefits the manufacturers of this vaccine technology – the US government has an endless need for new vaccines as the old ones expire.
My small hope is that the mRNA platform will be too costly to justify its continued use, as appeals concerning safety (or lack of) seem to fall on deaf FDA ears.
In the meantime, don’t believe the hype generated by ex-officials from the Biden and Trump administrations.
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Both Dr. Lena Wen, CNN correspondent, and Dr. Redfield, ex-director of the CDC, have gone on to mainstream media shows and promoted the narrative that the case fatality rate for avian influenza is over 50 percent. This, frankly, is a lie that the WHO is promoting. Bird flu generally is not tested for when someone has flu symptoms. When an outbreak of avian flu occurs on a poultry farm, testing of farm workers who are seriously ill will commence. This has led to the generation of the 890 case reports since 2003. Of those seriously ill patients reported to the WHO, over 50 percent died.
This is not an actual case fatality rate of avian flu around the world. It is, again, a sampling error due to a tiny data set derived from those who are at greatest risk due to general health. And just like the WHO reported on an exaggerated case fatality rate for mPOX, which was also based on a sampling error, or for Covid-19, again a sampling error, it is now used to justify psychological bioterrorism on the world population. Please don’t fall for it.
El Gato Malo on X succinctly points out that Dr. Leana Wen and her public health ilk are advancing:
1. Do more of the same lousy testing used in Covid-19 to overstate a disease and cause panic.
2. Develop another non-sterilizing non-vaccine that does not work to be pushed on “the vulnerable.”
3. Doing it “right now” under EUA, so whoever makes these tests and jabs can cash in and be shielded from liability.
4. Claiming that proxies like “triggers antibody production” demonstrate clinical clinical efficacy.
It’s just one last smash-and-grab for cash before the Brandon (Biden) administration ends. Anyone who falls for this one will truly fall for anything.
Question: what are Leana’s conflicts of interest? Who is paying her or giving her grants?
For those that haven’t viewed Dr. Redfield speaking of the avian flu case fatality rate, have a watch below. It is genuinely shocking. This fear-mongering comes from an ex-director of the CDC. Shame on him.
Frankly, it reminds me of the 51 intelligence officials claiming that Hunter Biden’s laptop was fake.
One has to wonder what conflict of interest motivated him to say this on national TV?
Remember in the US, there have been 62 cases of avian influenza discovered, and all but one case were very mild.
This deep dive into the supply chain issues is meant to show that public health has put itself into a groupthink situation that it can’t escape.
Many solutions to this quandary do not involve an evermore expanding schedule of vaccinations, stockpiled for some future use. I have some general thoughts before I sign off.
- The use of early treatments via safe, proven drugs is a good solution.
- We now have many antibiotics to treat bacterial infections. Vaccines do not always need to be our first defense.
- Our medical system is very good at treating infectious diseases. The risks from such diseases are much less than it once was. People do not have to live in fear of infectious disease. I like to ask people, how many people do you know have died of flu? If you know of any (I don’t), how old were they?
- The need to scare people into more and more vaccines is a dangerous trend.
- And yes, the more vaccinations one receives, the more likely an adverse event.
- Vaccinating pregnant women and babies should always be a last resort.
- It is time for Congress to rethink the vaccine liability laws.
Republished from the author’s Substack
Brownstone Institute
The Real Purpose of Net Zero
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From the Brownstone Institute
By
The recent Telegraph headline rang out of England recently with unsettling tones: Tenth of farmland to be axed for net zero
More than 10 per cent of farmland in England is set to be diverted towards helping to achieve net zero and protecting wildlife by 2050, the Environment Secretary will reveal on Friday.
Swathes of the countryside are on course to be switched to solar farms, tree planting and improving habitats for birds, insects and fish.
The move comes on the back of an aggressive and highly unpopular inheritance tax placed on generational farmers by British politician Rachel Reeves that has drawn sustained protest in the country. The commercial officer of Britain’s largest supermarket chain Tesco warned Reeves’ tax raid on farmers is placing “UK’s future food security is at stake.”
What if that’s the whole point? Tucker Carlson recently asked Piers Morgan this uncomfortable question.
Morgan refused to let his mind go there. And for good reason. It’s a dark premise. Yet one with historical context that must be analyzed due to the aggressive moves now in play against farmers around the world and humanity at large.
The British East India Company was the early template for the modern mega-corporate monopoly, globalization & vehicle to expand colonial power. Eventually dominating trade between Indian and Britain and far beyond. To say the company’s practices were ruthless would be putting it lightly.
Thomas Malthus was the East India Company’s first economist training individuals for service as administrators for the organization. Malthus was also a eugenicist in the economic wheelhouse of the world’s largest corporate monopoly with its own private army.
He wrote the following in his 1798 Essay on the Principle of Population:
The power of population is so superior to the power in the earth to produce subsistence for man, that premature death must in some shape or other visit the human race. The vices of mankind are active and able ministers of depopulation. They are the precursors in the great army of destruction; and often finish the dreadful work themselves. But should they fail in this war of extermination, sickly seasons, epidemics, pestilence, and plague, advance in terrific array, and sweep off their thousands and ten thousands. Should success be still incomplete, gigantic inevitable famine stalks in the rear, and with one mighty blow levels the population with the food of the world.
Eugenicists aren’t picky. Whatever gets people off the planet en masse – they’re into. Notice his last sentence, when bases are loaded and “success be still incomplete,” it’s the famine that is the preferred home run hitter – the weapon of choice.
In the 1860s, the full weight of the East India Company’s monopoly helped kill off India’s economy of textile industries putting countless out of work and forcing them into agriculture. This, in turn, made the Indian economy much more dependent on the whims of seasonal monsoons as dry seasons gripped the country.
The Indian and British press carried reports of rising prices, dwindling grain reserves, and the desperation of peasants no longer able to afford rice.
All of this did little to stir the colonial administration into action. In the mid-19th Century, it was common economic wisdom that government intervention in famines was unnecessary and even harmful. The market would restore a proper balance. Any excess deaths, according to Malthusian principles, were nature’s way of responding to overpopulation.
The current overlay argument government, NGOs, and global bodies like the United Nations are using to interrupt farming during present day is because of ‘net zero’ goals.
[See video below on the origin of the ‘climate crisis’ narrative highlighting the Club of Rome’s hand in crafting the modern day operation.]
Cows create greenhouse gases, carbon emissions from fertilizers, destruction of wildlife, and people themselves are all, we are told to believe, BIG negatives for the earth. Therefore they must be reduced.
Not in an orderly way, but as fast as possible because we’re told change in climate is the biggest, world-ending threat humans face – or something like that.
The United Nations [think Agenda 2030, Paris Agreement] has been the prime mover, policy-shaping action arm to accomplish this ‘net zero’ utopia. Enter Julian Huxley.
Huxley emerges after World War 2 as a crucial bridging figure from what has been referred to as “old eugenics” [Malthus] to a new eugenics based on molecular biology and human evolution.
In 1945 as World War 2 was ending, the United Nations was founded in New York. That same year, the United Nations Conference for the Establishment of an Education and Cultural Organisation (UNESCO) was also founded in London with Julian Huxley becoming the first Director-General.
One year later Huxley wrote UNESCO ITS PURPOSE AND ITS PHILOSOPHY stating:
At the moment, it is probable that the indirect effect of civilisation is dysgenic instead of eugenic; and in any case it seems likely that the dead weight of genetic stupidity, physical weakness, mental instability, and disease-proneness, which already exist in the human species, will prove too great a burden for real progress to be achieved. Thus even though it is quite true that any radical eugenic policy will be for many years politically and psychologically impossible, it will be important for Unesco to see that the eugenic problem is examined with the greatest care, and that the public mind is informed of the issues at stake so that much that now is unthinkable may at least become thinkable.
As it appears we are now in the home stretch of the environmental overlay of modern-day eugenics, the consensus-building and subtle messaging are being done away with.
A 2022 research article published in the journal Social Studies of Science titled Environmental Malthusianism and Demography writes:
Some bioethicists argue that, because ‘we are threatened with more population than the planet can bear’, humans simply ‘don’t have a right to more than one biological child’ (Conly, 2016: 2). Some recommend that governments act to uphold this limit (Hickey et al., 2016). Even feminist historians and sociologists of science, including some sharp critics of the population control projects of the late 20th century, now call for measures to reduce childbearing as a means of combatting climate change. Environmental Malthusianism, the idea that human population growth is the primary driver of environmental harms and population control a prerequisite to environmental protection, is experiencing a resurgence.
The current leadership of the UK, EU member states and the U.S. in regards to climate. Where Keir Starmer is racing to fulfill ‘net zero’ goals, as of last week, the U.S. has withdrawn from the Paris Agreement under the United Nations Framework Convention on Climate Change via executive order.
Without food, food production, and farming, there is famine. It’s that simple. The failed pandemic response was a reminder of that.
It has been assumed that leaders and policymakers, especially the United Nations, know these basic historical and current facts. Farmers are becoming endangered because of government policy to meet ‘climate goals’ and it’s being allowed to happen.
Republished from the author’s Substack
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