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Brownstone Institute

Kid Lab Rats

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13 minute read

From the Brownstone Institute

BY Thomas BuckleyTHOMAS BUCKLEY 

” (since [Covid] is universally mild in children), the risk-to-benefit ratio for the [Covid] mRNA injections in children is infinitely bad,” Baker said. “There is no ethical reason whatsoever to continue clinical trials of these products in children, and all such trials should be stopped.” “

Mommy, can I be a Covid lab rat?”

That is a request most parents will never hear and it is a request that very few parents would ever want to hear.

But, unlike the more typical “Can I have a pony?” request, letting your child be a Covid shot test subject is a request that can actually be granted around the nation.

Right now, for example, Pfizer/BioNTech is running an ongoing clinical trial to test the effectiveness of its shots (the shot is not a vaccine as it does not prevent catching the virus or transmitting the virus as typical vaccines do) on kids.

Pfizer has been running radio and other ads looking for test subjects; this is how they describe the study on their “Enrolling Children 6 to 23 months old for a COVID-19 Vaccine Study” website:

This study will help us learn how well our updated COVID-19 vaccine works in babies and toddlers who have not been previously vaccinated and see if the number of recommended doses can potentially be reduced for children under the age of 5. The study vaccine has been authorized by the United States Food and Drug Administration for children at least 6 months of age. It is designed to protect against the newer COVID-19 variant called XBB.1.5.

The company is also running similar trials for older kids and, of course, adults.

Clinical trials for drugs and procedures involving children are not inherently wrong and they are conducted safely around the world almost daily.

But this Covid trial stands out for a number of reasons.

First, the trial only involves kids who have never had a Covid shot before. The likelihood that a parent who has declined to get the shot for their kids in the first place will say “We chose not to get the shots for our kids, but feel free to experiment on them with the stuff we previously declined” is minimal.

In other words, if a parent didn’t feed their kid aluminum foil-flavored ice cream before it is highly unlikely they would feed their kid an experimental version of aluminum foil-flavored ice cream, even if you paid them (the trial comes with certain compensation enticements – Pfizer did not respond to a request for exactly what they are in this trial, though industry averages would indicate the pay would be between a few hundred to a few thousand dollars).

Second, there is the matter of “informed consent.” A trial subject must give permission freely, be told of any risks, and understand the entire situation. Clearly, nine-month-olds cannot do that.

It is perfectly legal for parents to give their “informed consent,” but here we get into the third problem: the risk/benefit question.

For example, during the pandemic (early 2020 to May 2023) there were 41 Covid deaths in California of kids under five. That number does not differentiate between “died with Covid” or “died from Covid;” that is a debate that continues to rage across the country and shall be put aside for the time being.

Every death of a child is a tragedy and this article is not intended to lessen that fact. However, children in general were not at all likely to get, let alone die from, Covid during the pandemic.

During the pandemic, there were about (rolling average) 2.4 million (about 6% of the total population) under-fives in California and there were about 385,000 cases of Covid reported in that age group.

Currently, about 3.2% of California’s under-fives have had the latest shot. That’s on par with the national average. What is interesting is that of the 70,817 kids who have received the shot in the state, 41,224 live in the Bay Area. In other words, the Bay Area has 20% of the state’s population, but 57% of the state’s “vaccinated” toddlers and babies. But do not ever think that politics has had nothing to do with Covid protocols.

During the pandemic, the overall likelihood of a child dying from/with Covid was about 1 in 60,000; for those over 75 – about 6.5% of the population or 2.7 million – there were about 51,000 with/from Covid deaths, or about 1 in 50.

The risk, clearly, is extremely different depending upon age and general state of health.

With a relative risk of being harmed by Covid, the risks of the Covid shot itself must be considered carefully – note: no kid in the study will get a placebo for comparison purposes.

The Covid shots, in the general population, did have significant side-effects and did cause a number of deaths. While these numbers are not broken out by age, in the same time period there were 640 deaths and 89,000 “adverse effects” experienced (much much more than just a sore arm) by Californians.

Also during the same time period, all other vaccines combined caused 66 people to die and 14,000 to have a reportable “adverse effect.” (Note – the numbers are taken from the CDC’s “vaccine adverse event reporting system,” a tool it stood by as an early warning device for decades…that is, until the Covid problem numbers got too high.)

That puts the general odds of something bad happening to a person after they get a Covid shot at about 1 in a 1,000 and some studies have shown it to be 1 in 800. In other words, the risk from the shot appears to outweigh the risk of Covid itself by a factor of 60 times.

Citing the uncertainty of benefit, it should also be noted that the European Union has not cleared the shot at all (with minor exceptions) for the under-fives and were hesitant in allowing them for the under 18s.

Clearly, the risk outweighs the reward, as it were, and it is unclear – because Pfizer did not answer any request for information/comment (see questions below) – if parents are given those figures when making the decision to enroll their kid in an experimental drug program.

Adults calculate risk and reward constantly – from “Can I make that light before it turns red?” to “Should I tease that lion?” But a seven-month old is simply not capable of doing so and while certain clinical trials do hold out serious hope and are important for society at large, a trial such as this for such a limited reward – kids very very very rarely get, let alone suffer seriously, from Covid – seems dubious.

In other words, if you wanted to test a new malaria drug you would not do so on Santa’s elves at the North Pole because there are no mosquitoes there to infect anyone.

According to the Belmont Report, which set baseline standards for human-involved clinical trials in the late 1970s (it was a government reaction to the horror of the CDC’s own “Tuskegee Syphilis Study”) one of the three core standards for justifying clinical trial testing is “beneficence.”

In other words, there is an obligation to protect persons from harm by maximizing anticipated benefits and minimizing possible risk and harm.

That risk/benefit calculation obviously changes in regard to other far more common childhood maladies, making participation in those studies potentially far more “beneficent.”

But in the case of Covid, the question is how are maximal, as it were, are the anticipated benefits?

Very very minimal and that is the problem, said Dr. Clayton Baker, former Clinical Associate Professor of Medical Humanities and Bioethics at the University of Rochester.

“Given the real and well-established risks of harm (including myocarditis and death), and given the functionally zero potential for benefit (since [Covid] is universally mild in children), the risk-to-benefit ratio for the [Covid] mRNA injections in children is infinitely bad,” Baker said. “There is no ethical reason whatsoever to continue clinical trials of these products in children, and all such trials should be stopped.”

Come to think of it, maybe just get the kid the pony instead.

Here’s a link to an on-going kids Covid study with a handy map so you can find a location near you (mostly Bay Area): A Study to Learn About Variant-Adapted COVID-19 RNA Vaccine Candidate(s) in Healthy Children

For clinical trials in general, you can look here for one that you might be interested in taking part in:

For clinical trials just about Covid, you can look here

As noted above, here are the questions Pfizer did not reply to:

-Exactly how is informed consent handled? I assume a parent/guardian can provide said consent?

-Do (or have) you run trials with previously vaccinated children?

-What child/youth trials have been run in the past and what have been their results?

-What is the compensation amount?

-Have any previous trials shown conclusively that the vaccine ameliorates Covid severity in children?

-When and in what manner did the FDA approve this trial?

-When do you expect to conclude the trial?

-Is this trial aimed at testing a “booster” shot or to cover a new variant?

-Has any child in any trial conducted had a significant and serious reaction requiring hospitalization and/or led to death?

-It appears one of the points of the study is to figure out how to cut the number of doses as well as check effectiveness. Is that correct?

-How many children – nationwide and in California specifically – have signed up for/been through the trial so far?

-What are the differences between trials involving children and those involving adults?

-Will Pfizer conduct trials each time it comes out with new variant vaccine shot?

Republished from the author’s Substack

Author

  • Thomas Buckley

    Thomas Buckley is the former mayor of Lake Elsinore, Cal. and a former newspaper reporter. He is currently the operator of a small communications and planning consultancy.

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Brownstone Institute

The Latest “Bird Flu” Psyop

Published on

From Brownstone Institute

By Robert W. Malone Robert Malone

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.

WHO Position Paper


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.

  • TdSanofi’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.

From the CDC website

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

Robert W. Malone

Robert W. Malone is a physician and biochemist. His work focuses on mRNA technology, pharmaceuticals, and drug repurposing research.

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Brownstone Institute

The Real Purpose of Net Zero

Published on

From the Brownstone Institute

By Jefferey JaxenJefferey Jaxen 

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. 

-BBC

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

Jefferey Jaxen

Jefferey Jaxen is a health journalist and featured in his weekly segment, ’The Jaxen Report’, on The HighWire. As an investigative journalist, researcher, and writer, Jefferey serves as Lead editor of The HighWire News and Opinion Team.Serving on the front lines of society’s shift towards higher consciousness since 2014, Jefferey is constantly working behind the scenes to spotlight the untold, censored and under-reported stories of our time.Covering Big Pharma corruption, the censorship complex created by social media giants and the underreported issues of drug and vaccine safety since 2014.

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