Brownstone Institute
The Vaccine Narrative Is as Leaky as the Vaccines
Let’s start with two simple questions. If regulators had the information available to them of the leakage between Covid-19 efficacy rates in controlled trials and their effectiveness in the real world, would they still grant emergency use authorization? Would their legal framework permit them to do so?
Remember, all laws serve a dual purpose. On the one hand, they are permissive and enabling, granting powers to do certain things. On the other, they are limiting and restrictive, ring-fencing what may lawfully be done even by the state.
Second, is Denmark being ruled by an anti-vaxxer government and health authority? From July 1 Denmark, which has an excellent health infrastructure including data collection, banned under-18s from being vaccinated and in mid-September the ban was extended to boosters for under-50s, other than in exceptional circumstances for immunocompromised and high-risk individuals in both cases.
The explanation offered by the health authorities is interesting both for what they said and what they did not say. They anticipate a rise in Covid-19 infections over autumn and winter and “aim to prevent serious illness, hospitalisation and death.” This risk applies to 50-year olds and above and not those younger. Because the vaccines are not meant to prevent infection, they will no longer be offered to the under-50s.
However, governments don’t ban products merely because they are not beneficial. Bans apply only to products that inflict harms. So the unstated reality is the benefit: harm ratio is no longer favorable. The really interesting question therefore is: why don’t they say so? The empirical data from around the world demonstrates negligible to negative vaccine effectiveness for healthy under-50s and greater risk of serious adverse events. Denmark’s decision marks official if implicit acknowledgment that harms are greater than benefits.
Baffling Origins of Lockdown
The lockdowns across the Western world remain, to me, inexplicable and baffling. The abandonment of a century’s worth of cumulative scientific knowledge and global and national pandemic preparedness plans were based neither on new science nor emerging data.
Rather, they were based firstly on apocalyptic modelling using flawed assumptions and secondly on dubious data from China whose authoritarian policies played to innate instincts in our own health bureaucrats and politicians, cheered on by the mainstream media. In a further nod to anti-scientific groupthink conformism, critical and contrarian voices within the health and political establishments were silenced and exorcised. Outside government, they were vilified and expelled from the public square in active collusion with the social media tech giants.
In February 2020, when the cruise ship Diamond Princess docked in Yokohama with 3,711 people on board, Kentaro Iwata, an infectious diseases expert at Kobe University, described it as a “Covid-19 mill.” Outbreaks seed easily on cruise ships because of the high numbers of susceptible elderly passengers living and socializing in confined quarters.
Even under these worst possible conditions, under one-fifth of the captive population was infected, a small number of the infected died and 98.2% recovered. Using age-adjusted data, Oxford University’s Centre for Evidence-Based Medicine estimated the infection fatality rate (IFR) of 0.5% and a case fatality rate (CFR) of 1.1% on the Diamond Princess and, as of March 26, 2020, a global IFR of approximately 0.20% (compared to the seasonal flu’s 0.1% and the Spanish flu’s >2.5% which killed mostly people in the 20–40 age bracket). Reassuringly, even for the over-70s without comorbidities, the IFR was below 1%.
All this ‘bullet proof’ data was thrown out in favor of completely unreliable data and fake videos from China that were then fed into mathematical modelling to produce apocalyptic scenarios that in turn were treated as forecasts by the media and governments. Madness.
India’s Experience: Vaccines Are Not Necessary for Beating Back Covid
India’s experience in mid-2021 proved that vaccines are not necessary for rapid mass recovery from a virulent Covid wave. Anyone who has followed the Covid narrative will remember the horrific pictures in spring-summer 2021 with bodies floating ashore on riverbanks and piling up in cremation grounds. The gradient was broadly similar during the curve’s ascent and descent, with the death rate reaching 1.06 per million people on April 20, peaking at 2.98 on May 21 and 23 and falling back to 1.00 on June 24 (Figure 1). On those three dates India’s full vaccination coverage was 1.26%, 2.96% and 3.53% of the population, respectively.
People questioned the reliability of the data, openly asserting a vast undercount in order to cushion the political embarrassment. Knowing something of India, I disagree and noted more than a hint of racism in the coverage. No matter. Even if the authorities deliberately suppressed the rising numbers of dead, it would be absurd to suggest they did the same with the downward numbers. The symmetrical rise and fall is consistent with the experience of most countries with successive waves of the virus. Whatever else might explain the fall, it certainly wasn’t high vaccination coverage. Herd immunity to the then-dominant Delta variant through a mix of uncontrolled infections and modest vaccination, possibly.
Another contender for the explanation is the widespread use of ivermectin. Mid-crisis in May last year, the state government of Uttar Pradesh (India’s most populous state with 200 million people!), boasted it had been the first to authorize large-scale prophylactic and therapeutic use of ivermectin against Covid-19 in May–June 2020. Studies were confirming that “the drug helped the state to maintain a lower fatality and positivity rate as compared to other states.”
A meta-analysis by Andrew Bryant and Tess Lawrie in the American Journal of Therapeutics of 24 randomized control trials (RCTs) in 15 countries (one of which was subsequently pulled as possibly fraudulent) concluded that ivermectin significantly helps to prevent and treat Covid-19 and, with a 62% mortality reduction, can potentially save millions of lives. They published a follow-up analysis in the same journal that removed the suspect study and the results still showed robust ivermectin efficacy.
An analysis of seven RCTs, covering 1,327 patients, by Swedish physician Sebastian Rushworth found “a 62% reduction in the relative risk of dying among Covid patients treated with ivermectin.” A recent large-scale study from Brazil published on August 31 found that, compared to regular users, non-use of ivermectin increased the risk of Covid-related mortality by 12.5 times and dying from Covid by seven times.
Yet for some strange reason, Western health bureaucracies would neither recommend ivermectin – a low cost, off patent and no profit drug for Big Pharma – nor fund a rigorous but fair (that is, not designed to fail) clinical assessment of its efficacy against Covid. It had morphed into Voldermectin: the drug that must not be named.
Global Experience: Vaccines Are Not Sufficient to Beat Back Covid
My earlier articles show why Australia’s Covid numbers this year demonstrate that vaccines are not sufficient to prevent mass infections, hospitalization and deaths either. Steve Kirsch alerted his Substack subscribers on September 17 to an internal report for the governing Liberal Party of Canada back in June. It makes for depressing reading that will come as no surprise to all of us who have grown increasingly cynical about public health authorities and governing elites. The report draws on official Ontario data, is informed by wide international scholarship and emphasizes that the empirical results are in line with trends in other Canadian provinces and countries.
The fully vaccinated show rise in hospital admissions within 5-6 months; the boosted, within two weeks and rising thereafter for several months. Immunity through natural infection can last up to 20 months. Vaccination shows considerable benefits to over-70s and some benefit to over-60s but virtually no benefit to under-60s with respect to hospitalization and mortality rates. By contrast, adverse events are concentrated in the 18–69 age groups, and especially, in order of most to least, in the 40–49, 50–59 and 30–39 age groups.
Because the “abundance of data” demonstrates that vaccines do not prevent infection, transmission, hospitalization and deaths for the under-60s, “public health policy tools such as, mass vaccination campaigns, mandates, passports and travel restrictions need to be re-evaluated for relevance.” Factoring in also “known adverse events and unknown long-term effects,” the “empirical evidence investigated in this report … does not support continuing mass vaccination programs, mandates, passports and travel bans for all age groups.” The government has sat on this report since June – what a surprise.
Meanwhile there continues to be very little evidence in the real world that countries with high rates of multiple vaccine doses suffer correspondingly lower rates of Covid-19 mortality (Figures 2 and 3). In the two charts, Chile has both the highest booster rollout and the highest Covid-related death rate per capita, while India has the lowest booster coverage yet the second lowest mortality rate.
Some experts point to a worrying trend of rising excess mortality among under-14s in 28 European countries. An article in Vaccine – downloaded more than 110,000 times in preprint – seems to suggest, albeit tentatively, that added risks of serious adverse events are 2.4 and 4.4 times higher than the reduced risk of hospitalization for Moderna and Pfizer vaccines, respectively. Cautioning that the harm-benefit ratio will vary with populations at different Covid risk profiles and in different time periods from the Moderna and Pfizer studies they analyzed, the authors conclude with the need for large, randomized trials to come to robust conclusions. It would help if Moderna and Pfizer would release the granular, individual level data in their possession.
In a follow-up note on Substack, two of the study’s authors note that the normal rate of adverse events for other vaccines is 1-2 per million. The swine flu vaccine (1976) was pulled after it was associated with Guillain-Barre Syndrome at a 1 in 100,000 rate. By comparison, the Pfizer and Moderna clinical trials show 125 adverse events per 100,000 vaccinated people, while preventing between 22-63 hospitalizations.
Another new study of almost 900,000 5-11-year-old children in North Carolina, published in the New England Journal of Medicine, adds to concerns that vaccines don’t just lose their effectiveness in just a few months; they also destroy natural immunity against reinfection severe enough to put them in hospital.
Panels C and D (the study’s authors use “Panel” rather than “Chart”) clearly show that among people infected by the Delta variant, protection against reinfection of the unvaccinated lasts longer than of the vaccinated. The former’s effectiveness was still above 50% eight months later in May 2022 while the latter’s had fallen to zero (Figure 4). But with the Omicron variant, the previously infected are slightly better off vaccinated than unvaccinated after two months (94.3:90.7%) and much better off after four months (73.8:62.9%). The likely, albeit not definitive, explanation is that the vaccines themselves are destroying the protection provided by natural immunity.
Three comments about Panels E and F (Figure 5). First, while the x axis for Panel E is in weeks, Panel F’s is in months. So the first visual impression is misleading. Second, the maximum effectiveness of a vaccine against a reinfection severe enough to require hospital admission is around 88%, reached approximately four weeks after the first dose is administered. By contrast, the initial effectiveness of a previous infection is 100% and remains above 95% (remember the vaccine’s much-touted 95% efficacy rate?) until seven months later.
Third, the effectiveness of a previous infection against reinfection requiring hospitalisation does not decline to the same level as the vaccine’s peak effectiveness until nine months after infection. This is the reality that the CDC denied until recently and used as the justification for discriminating between the vaccinated and unvaccinated for access to public spaces.
Three conclusions follow:
- The risk of severe outcomes for children from infection by current Covid variants is low;
- The risk of severe adverse reactions from vaccines is higher, meaning vaccination is a net harm for young children – exactly why Denmark has banned them for children;
- Exposing healthy children to the risk of infection may be better for both individual and herd immunity than mass vaccinating them.
The FDA is not likely to restore its credibility as the US regulator with the widely ridiculed revelation that the new bivalent boosters were authorized on the basis of trial results from eight mice. Professor Marty Makary from the Johns Hopkins School of Public Health tweeted his concerns about this and also about the announcement of an annual Covid vaccine that is not data-driven and ignores natural immunity as well as the risks of immune imprinting (where the immune system remembers its initial response to infection or vaccination in a way that usually, but not always, weakens the response to future variants of the same pathogen) from a multi-dose vaccination strategy.
From mRNA Vaccine Hesitant to Anti Vaxxer
The Financial Times – as mainstream establishment as they come – recently warned that the US decision to roll out new booster shots without clinical testing on humans – already dubbed the mouse vaccine by some – risks undermining public trust and deepening vaccine hesitancy. “We already have a trust problem in this country and we don’t need to make it worse,” Eric Topol, founder and director of the Scripps Research Translational Institute, said. Yet, even while bemoaning the loss of public trust in health experts and institutions, Topol just couldn’t help himself and smeared the Covid vaccine hesitants and sceptics as “anti-vaxxers, anti-science” people.
He thereby demonstrates precisely the pathology so beautifully described by Julie Sladden in an article in Spectator Australia on September 8. The Tasmanian doctor, “Having probably received more vaccines than most, given I am both a doctor and fairly well travelled,” used to begin her apology for refusing the Covid jab with “‘I’m no anti-vaxxer!’” However, after two years of “government-endorsed segregation and dehumanisation of those who exercised their right to refuse the jab,” she has changed her mind.
If an “anti-vaxxer” is someone who cannot give informed consent to a “vaccine” that fails to prevent infection or transmission, has alarming safety signals, must be taken to earn back the right to live and work in society, for a disease that has a greater-than 99 per cent survivability rate, then “yes,” I’m an anti-vaxxer… My government made it so.
To this we should add the very high likelihood of crossover vaccine hesitancy to other vaccines. In my own case before the pandemic I have dutifully gone in for the annual flu shot strongly recommended for my age demographic. Not any more. The Covid experience killed my trust in the medical and public health establishment and, having done my own research, I now politely decline the annual pre-winter flu shot.
Author
From Brownstone Institute
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?
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.
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
Author
From the Brownstone Institute
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
Author
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