Some UK military personnel and their families have been turning to food banks because of the increasing pressures from the cost of living crisis, a British news network has reported.
The raging cost of living crisis that has had the UK in its stifling grasp is going to cause thousands of extra deaths this year, according to new research, as life expectancy across the UK will plummet by 6.5 percent this year.
The research suggests that untimely mortalities in the United Kingdom are expected to rise from 463 to 493 per 100,000 inhabitants.
The findings have shone a light on critical concern for the populace at large. The unrelenting cost-of-living crisis, combined with a prolonged period of soaring prices, is anticipated to result in a significant 6.5 percent drop in life expectancy throughout the nation this year.
Furthermore, the report highlights a stark disparity: the most economically disadvantaged households are projected to face a four times higher death toll than their wealthier neighbours. This discrepancy arises from the fact that the less affluent must allocate a more significant portion of their income to pay for energy, the cost of which has rocketed.
Recent statistics from the previous month indicate that the UK’s inflation rate stood at 6.7 percent. Despite this reduction from its peak of 11.1 percent, Britain continues to have the worst inflation of all G7 member states.
“The mortality effects of inflation and real-terms income reduction are likely to be large and negative, with marked inequalities in how these are experienced. Implemented public policy responses are not sufficient to protect health and prevent widening inequalities,” researchers noted.
These findings come on the heels of a recent alert from the UK-based consumer association ‘Which’ last month, when it pointed out that rising food prices had left low-income households in the country in dire straits and having to make painful decisions about whether to pay the utility bills or put food on the table.
During the 1950s, the inactivated polio vaccine created by Jonas Salk was made using rhesus monkeys that were infected with SV40, a monkey virus that was later linked to cancer in humans.
From 1955 to 1963, hundreds of millions of people worldwide — in North and South America, Canada, Europe, Asia and Africa — received the vaccines, which at the time were heralded as a medical breakthrough.
In the archived 1956 video below, you can see a propaganda piece from that era, showing just how the ill-fated vaccine was made.
“Few back then grasped that these vaccines might also be a huge, inadvertent, uncontrolled experiment in interspecies viral transmission,” a 2004 article in The Lancet noted.
1950s propaganda reveals how polio vaccine was made
While Salk’s polio vaccine was considered a medical triumph of its time, its manufacturing process leaves much to be desired.
“Welcome to modern vaccinology. A hilariously unscientific process predicated on insane barbarism, rife with fraud and immense hubris,” Inversionism wrote on X, formerly Twitter.
The investigative journalist detailed the polio vaccine’s manufacturing process outlined in the video as follows:
Put all the glassware inside a hot steam bath or sterilize it.
Import Macaca mulatta monkeys from India for the experiments.
Prepare a mixture called “medium 199” — containing 2% calf serum, 200 units/ml penicillin, 200 g/ml dihydrostreptomycin and 50 units/ml Mycostatin (nystatin Squibb); the pH of the medium was brought to 7.0 by the addition of a NaHCO3 solution.
Euthanize the monkeys, remove their kidneys, and then place the kidney into a tube and hand-mince it with scissors into small bits.
After the kidney tissue was weighed and decapsulated, they put the tissue in a centrifuge tube where they washed it in phosphate-buffered saline and placed it in a trypsinization flask. Trypsin enzymes break down the proteins, which were then centrifuged at 800-1000 RPM for 10 minutes to separate the tissue and cells.
The kidney cells are then mixed with the medium 199 and incubated (fermented, rotted essentially) at 37C for 6-8 days. By the end of the 6-8 day period, the bottles and tubes were covered with a “confluent sheet of cell growth.”
Once the medium 199 is exhausted, half is siphoned off to be replaced by fresh medium 199.
They then add the “polio virus” for the first time. 3 different strains supposedly, with no other details on the source, isolation process, or genome determination.
The bottles continue to rock for 4 days in the solution culturing, fermenting and decaying, and then it’s ready for harvesting.
Scientists then visually look at the vials under a microscope to do a “titration test” to discern how much live virus is in the solution, hand counting particles that could be ANYTHING. (very scientific …)
Next is filtration, the most egregious part. They filter the solution first through porcelain filters (heavy metal risk), and then through MULTIPLE SHEETS OF ASBESTOS to drain out any kidney tissue or stray bacteria.
(This part of the process is not disclosed in the video but is detailed in the original paper on the polio vaccine process. They made multiple trivalent vaccine pools, with some having additional additives like sodium bisulfite, along with parabens, a known carcinogen and endocrine disruptor).
Now rabbits, monkeys, guinea pigs, and chickens are injected with the “live virus” vaccine solutions … to ensure it’s free of other pathogens.
Now the “climax” of the process as they call it, inactivation. This is where they mix the vaccine solution with formaldehyde, and then let it sit together for 66-68 hours. The narrator then hilariously says “then what remains can only do good, can provide humans with protection of paralytic polio.” “The enemy of man can now become his servant.”
Then the process of mass distribution. They get these massive tanks and mix in all the solutions, adjuvants, chemicals, and ingredients for mass production and “preservation.”
Before mass administration, they do a couple of experiments on mice and monkeys to ensure the vaccine is creating enough “polio-fighting antibodies” in humans.
The remainder of the process details the various “tests” they do as the vaccine lots are distributed, before really turning up the propaganda and showing President Eisenhower’s son receiving the polio vaccine.”
Paralyzed children, deaths reported following vaccination
By 1954, a large-scale study of Salk’s polio vaccine, which included 1 million children, took place. On April 12, 1955, Salk declared the shots to be safe and effective. In addition to being given widely throughout the U.S., by 1959, 90 countries were using it.
But there were signs of problems from the start.
After mass vaccination began, some subjects became paralyzed in the limb where the vaccine was given. Recalls of 250 cases of the shots from two laboratories ensued following the reports of parasitic illness.
“There were also reports of paralysis and death in several children,” Singapore Medical Journal reported. “Investigations showed that improperly inactivated vaccine had released live virus into more than 100,000 doses of the vaccine.”
“When Salk developed his vaccine, instead of using human tissues, as did the scientists who won a Nobel Prize for first growing poliovirus in tissue culture, he used minced-up rhesus macaque monkey kidneys, which were remarkably efficient poliovirus factories.
“Those who sought to supplant Salk’s formaldehyde-inactivated vaccine with live, attenuated oral vaccine also used monkey kidney cultures. Despite a manufacturing problem that, at best, left six children who received the vaccine paralyzed in the arm, and despite concerns about wild simian viruses, Salk’s shots were declared safe and effective after 1954 field trials.
“The next year, after grudging approval by skeptical government regulators, free Salk shots were made available throughout the USA. By 1960, scientists and vaccine manufacturers knew that monkey kidneys were sewers of simian viruses.”
Americans kept in the dark about monkey virus in polio shots
It was 1959 when the late Bernice Eddy, a researcher at the National Institutes of Health, conducted a study, injecting hamsters with the rhesus monkey kidney substrate used to make the polio vaccines. The majority of them developed tumors.
“Eddy’s superiors tried to keep the discovery quiet, but Eddy presented her data at a cancer conference in New York. She was eventually demoted, and lost her laboratory,” The Atlantic reported, but soon after researchers with Merck pharmaceutical company identified the cancer-causing virus in rhesus monkey kidney cells, naming it SV40 because it was the 40th monkey virus discovered.
According to Barbara Loe Fisher, co-founder and president of the National Vaccine Information Center, in a presentation before the U.S. House of Representatives in 2003:
“Sadly, the American people were not told the truth about this in 1960. The SV40 contaminated stocks of Salk polio vaccine were never withdrawn from the market but continued to be given to American children until early 1963 with full knowledge of federal health agencies.
“Between 1955 and early 1963, nearly 100 million American children had been given polio vaccine contaminated with the monkey virus, SV40.”
Did SV40 in vaccines cause cancer?
While there wasn’t an “epidemic” of cancers that followed the widespread administration of polio vaccines contaminated with SV40, which suggests the virus alone may not be causing the cancers, researchers noted, “it seems possible that SV40 may act as a cofactor in the pathogenesis of some tumors.”
As further reported in Oncogene, at least three independent scientific panels agreed that “there is compelling evidence that SV40 is present in some human cancers and that SV40 could contribute to the pathogenesis of some of them.”
For instance, research published in the New England Journal of Medicine in 1992 revealed that half the choroid plexus tumors and most of the ependymomas studied contained a segment of the T-antigen gene related to SV40.
“These results suggest that SV40 or a closely related virus may have an etiologic role in the development of these neoplasms during childhood,” the researchers wrote.
In 2002, meanwhile, The Lancet published evidence showing SV40 is significantly associated with some types of non-Hodgkin lymphoma after detecting it in 42% of non-Hodgkin lymphomas tested.
And in a 2004 review of the then-available evidence, it’s noted:
“Persuasive evidence now indicates that SV40 is causing infections in humans today and represents an emerging pathogen.
“A meta-analysis of molecular, pathological, and clinical data from 1,793 cancer patients indicates that there is a significant excess risk of SV40 associated with human primary brain cancers, primary bone cancers, malignant mesothelioma, and non-Hodgkin’s lymphoma.”
What else is lurking in vaccines?
While the SV40 polio vaccine contamination occurred decades ago, the controversy continues, as does the potential for present-day vaccines to be contaminated.
Research by cellular and molecular biologist Judy Mikovits, Ph.D., showed that many of our vaccines are contaminated with gammaretroviruses.
How did this happen?
In short, vaccine viruses were replicated and grown in animal cell cultures that were already contaminated with retroviruses. In other words, the root of the problem stems from the use of contaminated cell culture lines, similar to the problems with the original polio vaccine.
Meanwhile, microbiologist Kevin McKernan — a former researcher and team leader for the MIT Human Genome project — assessed the nucleic acid composition of four expired vials of the Moderna and Pfizer mRNA COVID-19 shots.
“DNA contamination that exceeds the European Medicines Agency (EMA) 330ng/mg requirement and the FDA’s 10ng/dose requirements” was found.
In addition to the spike protein and mRNA in COVID-19 shots, McKernan’s team discovered SV40 promotors.
McKernan explains that in many cases, when tumors are sequenced they’re found to contain sequences from SV40 and other viruses, which can integrate into your genome, causing disruptions and instability that can trigger the cell line to grow out of control.
In the case of COVID-19 shots, he says:
“The concern is if this DNA integrates the genome, one portion of the SV40 sequence is an SV40 promoter, a very strong promoter, which means it drives transcription wherever it lands in the genome.
“If this happens to drop itself in front of a proto-oncogene [a gene that has the potential to cause cancer] and drives a lot of expression off of a gene that’s known, if you hyper-express it and turn the cell cancerous, then we have a concern that DNA is in fact doing that.”
McKernan and colleagues have tried to spread the word about SV40 promotors and components in COVID-19 shots, but the media continue to try to discredit their findings,
much like what occurred with SV40 in the original polio vaccines.
Further, as for why the SV40 promoter and enhancer are in COVID-19 shots in the first place, it’s again related to the plasmid growth medium, which in this case is E. coli.
Since many types of cells continue to be used as growth mediums during vaccine production, including animal cell strains from chickens, dogs, monkeys, hamsters and insects, as well as cells from bacteria or yeast, and vaccines continue to be fast-tracked to market, it’s more important than ever for scientists and manufacturers to ensure that the treatment or preventative isn’t causing more harm than good.
Firstly, Binder writes, “The effective dose of the expressed foreign protein is unknown and varies greatly between individuals, mRNA ‘vaccines’ should never have been approved.”
Secondly, “The cells that express the protein foreign to the body and then present it on their surface are falsely recognized by the immune system as being foreign or infected by an alien, thus are destroyed in an autoimmune attack similar to transplant rejection.”
He continues: “If it was only expressed by skeletal muscle cells capable of regeneration, this would not be problematic. But the LNPs [lipid nanoparticles] are chosen in such a way that they introduce the mRNA into any body cell, including those of the heart, brain, embryo and fetus. Worse: As physiological doses did not induce a relevant immune response, a horrendous dose of mRNA was chosen, which can lead to the destruction not only of a few, but of so many cells that this can cause serious illness and death. Worse: The chosen antigen and LNPs are themselves toxic.”
He notes: “Kevin McKernan found contamination with up to a third of functional bacterial plasmid DNA from the manufacturing process, which explains the spike expression over years detected by pathologists.” Finally, it has not been ruled out yet that the DNA can be integrated into the genome and even be inherited by offspring.”
The US Food and Drug Administration (FDA), quick to approve an experimental and untested Covid-19 ‘vaccine’, is now stalling over approval of a new device that could save the lives of people who go into anaphylactic shock.
One of the first lines of treatment for anaphylaxis is an EpiPen which can be carried by those who know they have allergies. It is a device containing the drug noradrenaline (called norepinephrine in the US) that counteracts the shock induced by anaphylaxis. However, an EpiPen requires the injection of noradrenaline intramuscularly. This is invasive and if the person is unable to administer the drug others can be reluctant, either not knowing how to use the device or being afraid to. Also, the drug has to get from the musculature to the bloodstream to be effective. This can take five to ten minutes during which time the person may die.
How much better if noradrenaline could be administered more directly into the bloodstream. Manufacturing a device to do this intravenously, far less expecting anyone other than a medic, nurse or paramedic to have the expertise to do this in an emergency, is a tall order. But drugs can be administered rapidly into the bloodstream nasally and a company, ARS Pharmaceuticals, has developed an injection-free device for administering noradrenaline nasally in the form of an epinephrine nasal spray.
What’s not to like, you may think. Well, the FDA don’t like it and have withheld approval pending further testing. The FDA objections are based on the need for further clinical data in people with anaphylaxis due to the fear that it may fail to work.
It is, surely, heartening that the FDA has the best interests of potential anaphylaxis sufferers at heart. If only they had had the same concern on 2021 when they approved the Pfizer Covid-19 vaccines. It has been exposed in these pages from the start of the Covid-19 vaccine rollout that these were ‘experimental’ medications and had not been tested adequately before approval. Well, they have been tested now and the outcome is clear: they were completely unnecessary; they do not work; and they are extremely dangerous leading to injury and death. They undoubtedly have played a large part in the level of excess deaths observed in recent years.
According to UK government figures, the overall fatality rate from Covid-19 (always a disputed figure due to the difficulty in distinguishing ‘with Covid’ from ‘from Covid’) is 0.1 per cent. The estimated fatality rate from anaphylaxis – made uncertain by the fact that many suspected cases are dead before being found – is between 0.7 and 2 per cent. Recent England hospital Covid-19 admissions are approximately 3,000 per month at the latest available figures. The annual rate of hospitalisation in England for anaphylaxis in 2022-23 was 26,000; at approximately 2,000 monthly, the same order of magnitude as the Covid-19 admissions.
Bearing in mind that it is not easy to distinguish Covid-19 from other respiratory infections but that anaphylaxis is unmistakable and more fatal and, assuming a similar situation in the US, the recent FDA decision regarding nasally administered noradrenaline for anaphylaxis in the light of their unseemly haste over Covid-19 vaccinations is hard to understand. Could political and financial pressured be involved? Surely not!
On August 31, 2023, roughly two weeks before the latest COVID booster recommendation by FDA/CDC/ACIP, independent researchers published an online, open-access analysis announcing “… it is possible to distinguish, by tryptic digestion, followed by mass spectrometry analysis, synthetic Spike proteins originated from the translation of the mRNA vaccines from natural Spike circulating in biological fluids.”
In other words, the researchers devised a method to determine how long the synthetic spike protein created by mRNA vaccines was present in the human body of vaccinated individuals.
This was a big deal. Their approach represents the first proteomic detection of recombinant Spike in vaccinated subjects. How long did they find it lasted?
They write, “The specific PP-Spike fragment was found in 50% of the biological samples analyzed, and its presence was independent of the SARS CoV-2 IgG antibody titer. The minimum and maximum time at which PP-Spike was detected after vaccination was 69 and 187 days, respectively.” Below is a chart from their study comparing the detection of the spike protein in the body of vaccinated and “after infection non vaccinated.”
The FDA and CDC’s Advisory Committee on Immunization Practices (ACIP) didn’t care and approved the new COVID booster anyway calling for yearly boosters ‘like the flu shot.’
The mRNA vaccine technology used against a circulating coronavirus is a new, never-before-used approach and method. Proper safety testing and an understanding of what happens when you repeatedly inject billions is unknown. Why the approval? Well because it was an emergency we were told… we just didn’t have time. You understand right?
Yet, with the newly updated booster announced by the CDC for 6 months and older, with no exceptions we are still aggressively injecting. Why? America is the outlier with its cavalier approach to experimenting on its population as new warnings appear almost weekly from this injectable tech platform.
The CDC states mRNA vaccines use mRNA created in a laboratory to teach our cells how to make a protein that triggers an immune response inside our bodies. The Covid vaccine’s one and only purpose is to create that spike protein. It has only one job.
Do you think regulators or the pharmaceutical companies making the shots cared to understand what else that spike did after it was created or how long it persisted?
Pfizer’s Nonclinical overview submitted to FDA’s Center for Biologics Evaluation and Research, a document which doctors had to sue the agency in court to obtain, states:
“The protein encoded by the RNA in BNT162b2 is expected to be proteolytically degraded like other endogenous proteins… Therefore, no RNA or protein metabolism or excretion studies will be conducted.”
In other words, we aren’t going to bother looking because one can’t find what one doesn’t search for.
Two years later, public assertions like the one from The Infectious Disease Society of America still regularly repeated estimates that the spike proteins generated by COVID-19 vaccines last up to a few weeks.
“I’ve asked this before and I just don’t have a clear idea about how long the spike protein the messenger RNA in our bodies produce… how long has it been detected in patient serum or tissues or even in animal studies? Do you know how long it may persist in blood or serum or tissues?”
To this question, Rituparna Das, Moderna’s Therapeutic Area Head of Respiratory Vaccines and the company’s ACIP lead answered:
“The spike protein, ah, availability I believe is on the order of days, but, like less than a week. But I will confirm that with our tox [toxicology] folks as well.”
No one knew for sure, not even the injectable product’s manufacturer, and more importantly, no one cared to know.
Yet the spike continued to turn up as the culprit in more pathogenic insults to humanity. In 2023, researchers reporting circulating spike protein detected in post–COVID-19 mRNA vaccines myocarditis stated:
“A notable finding was that markedly elevated levels of full-length spike protein, unbound by antibodies, were detected in the plasma of individuals with post vaccine myocarditis, whereas no free spike was detected in asymptomatic vaccinated control subjects”
The CDC/ACIP response was that the benefits outweigh the risks… simplistic, insulting, and lacking transparency talking down to the people being targeted by this novel shot.
The authors of the August 2023 suggested that the spike protein may be integrating into the human cells. A similar, and in ways more detailed, warning was just given by well-respected cancer genomics researcher at the University of South Carolina Phillip Buckhaults, Ph.D. during his recent testimony in front of the South Carolina Senate Medical Affairs Committee which he stated, among other things, that:
The Pfizer mRNA vaccine is contaminated with the plasmid DNA vector that was used as the template for in vitro transcription reaction.
This DNA could cause rare but serious side effects like death from cardiac arrest.
The DNA can and likely will integrate into the genomes of transfected cells.
There is a very real hazard for genome modification of long-lived somatic cells, which could cause sustained autoimmune attacks towards that tissue.
There is also a theoretical risk of future cancer, depending on the piece of DNA and site of integration.
The CDC’s website states the following outdated and scientifically lazy explanation, at best, of what happens to human DNA after being injected with COVID-19 shots.
According to Professor Buckhaults, this is just not true… at all.
Two further points raised by Professor Buckhaults were first, that the plasmid DNA contamination was not present in the material used in Pfizer’s initial vaccine trials for regulatory approval. It was only after approval and rapid scale-up of manufacturing did the company used questionable, scientifically reckless techniques which led to the contamination. Second, Professor Buckhalut’s lab, a world leader in this type of research, estimates that each vaccination contains about 200 billion pieces of plasmid DNA encapsulated in the lipid nanoparticle.
We know it is now a basic technique to find the synthetic spike in vaccinated individuals. Perhaps even more troubling, it’s basic genetic research to find out if the plasmid DNA is integrating into and forever changing the DNA/genetics of vaccinated individuals yet health agencies and labs just don’t seem to want to look.
With the CDC clearly not willing to do even the most basic steps to regain the public trust lost, as new director Cohen claimed was her main goal, the public must back away further from an apparently rogue government body. As prominent scientists and doctors denounce the agency and its products, we have hit breakaway speeds into historically uncharted territory as public health agencies, once a fixture running in the background of America, have become a cyclic, menacing threat with each new booster rollout campaign.
I listen attentively when doctors and other health professionals who once shilled for the covidian tactics of ‘sheltering in place’ (what a quaint euphemism for imprisonment!), masks (how much more evidence do we need to show that they are and always have been useless for viral respiratory pathogens?), and, of course, the innovative mRNA-based jab, all the while never caring to spare a breath for natural immunity or early treatment, have a change of heart.
Well, after a bit of travelling down their personal roads to Damascus and seeing a light strong enough to make them revise their former gospels, they have had their conversion, have joined our side and are now front and centre on the resistance pulpit.
I acknowledge that we need all the help we can get and I am grateful for their assistance, but I am often mindful that the explanations offered by some of them, in their hindsight, only go so far. In fact, they fall far short of an appreciation that the whole phoney covid pandemic was an ‘operation’ perpetrated upon the globe by a powerful faction that sought not only to enrich their already rich selves but to enslave us and, with their bioweapons, to kill and maim.
It wasn’t just a matter of Pfizer, Moderna and Astrazeneca licking their chops at the opportunity to make wild profits by pushing an inadequately tested agent while nervous health officials erred on the side of ‘vaccinating’ everyone who breathed as a precautionary measure based on fearful and ignorant worry … No. It was more, it was more profound, it was more devilishly destructive and centrally planned.
Yes, there was — there is — a conspiracy, not just organic goosestepping and Sierpinski triangles. It was a bunch of high-placed people who set about controlling and literallydestroying a large swath of the world’s population, deliberately, and relentlessly.
They are still going at it and with more than just the lethal Jab. The ‘reset’ they planned includes widespread censorship, the destruction of foundational principles of medicine, digital identification, social credit permissions, total surveillance, a fraudulent climate ‘emergency’ leading to further restrictions upon human autonomy, and, naturally, more and more inoculations. The scale of their operation is immense and its fruits should be visible by now to anyone who dares to think.
Ignorance and corporate greed are not the prime movers. Not to finger the Globalist Cabal for the murderers they are is to let them off the hook and to dissipate the energies of our resistance. Not to connect the dots is to be left with a picture so incomplete that responsibilities are diffused and the most significant guilty parties are at leisure to continue their machinations unscathed.
I chanced to have a conversation with a health practitioner the other night, a person who had been coerced into the Jab to preserve his job, a person who joined us at Parliament here in Wellington as we protested the mandates, a person who has worked behind the scenes to assist others in the health care system who opposed the regimen of masks, quarantine and jabs. When I asked him point-blank whether he thought there was indeed a ‘depopulation agenda’, he shook his head. It was the proverbial bridge too far, but it gave me an idea.
Those celebrated doctors and nurses, familiar to MSM audiences as mouthpieces for the Programme at the outset, who influenced countless people to toe the line — what if they, in their new shining garb within the freedom community, painted the full picture?
I still can’t explain how any self-respecting health professional could have lost his or her wits so completely in 2020 so as to have discarded the principles of their discipline. Could they really have forgotten about natural immunity and early treatment and the need for a genuine vaccine to be tested over years for safety and efficacy?
But never mind. If our new apostles of good sense can now use their heft and influence to enlighten the many who waver in the middle about the true extent and depravity and the planned coordination informing the covidian psyops, they will have atoned for their earlier lapses and complicity. But unless they have the courage to go that far, I, for one, will regard their intentions with grave suspicion.
Unless they have the guts to serve up the whole enchilada, they can take their morsels elsewhere.
However hard Big Pharma is pushing the new Covid jabs, investors know the truth.
Even though we are getting closer to winter, a perfect time to sell Covid jabs, Moderna’s share price is down 44%.
And Pfizer’s is down 36%.
Clearly investors in the know realise that people just aren’t taking the Covid shots anymore.
So the sales team has been brought in to try and drum up business. All over the MSM news today are reports of a new study which claims to show that Long Covid can cause long-term damage to multiple organs.
The study, published in The Lancet is titled “Multiorgan MRI findings after hospitalisation with COVID-19 in the UK (C-MORE): a prospective, multicentre, observational cohort study”.
Read any MSM coverage of this study and you will be led to believe that a third of Long Covid patients sustained damage to multiple organs five months after infection. Lung injuries were almost 14 times higher among Long Covid patients, whilst brain and kidney injuries were three and two times higher respectively.
‘Study lead Dr Betty Raman said people who had more than two organs affected were “four times more likely to report severe and very severe mental and physical impairment”’.
Scary stuff, sign me up for my booster now.
But is the study all that it is made out to be?
First of all the declarations of interests page is over 1,600 words long with reference after reference to links with Big Pharma.
Secondly, and most importantly, the study is massively flawed. It recruited 2,710 participants and whittled these down to 259 who were discharged from hospital with PCR-confirmed or clinically diagnosed COVID-19 between March 1 2020 and Nov 1 2021.
This group was then compared with 52 non-Covid-19 controls from the community. The average age of the study group was 57 and the control group was 49. As the study says, “compared with non-COVID-19 controls, patients were older, living with more obesity and had more comorbidities”. 50% of the study group were obese compared with only 37% of the control group. 40% had smoked at some point in their lives compared with only 17% of the control group. I could continue with percentages of all the pre-existing comorbidities but I think you get the picture.
(For those who will ask the question, 40% of the control group were vaccinated at follow-up compared with 44% of the study group.)
So what do you think happens when you take an unhealthy, older group of people who have been in hospital with Covid and you compare them with a younger, healthier group of people from the community. You geniuses, you guessed it. You find that the unhealthier group are unhealthier.
Give the Big Pharma sales team a genius medal for that one and a sucker medal to the MSM who did the sales pitch for them.
But don’t take it from me, here is what Professor Francois Balloux, Director of the UCL Genetics Institute in London, has to say about the study:
Thus, my point is not that the conclusions of the study are necessarily false but that the control group is inadequate. I worry the study may have been published as is because it fits a particular narrative, and not necessarily because it is sound and robust.
By choosing a control group made of elderly, frail, terminally ill patients, it might be possible to demonstrate that Covid actually repairs organ damage, which would obviously be an absurd conclusion, and which should rightly be called out. Yet, here we are …
There is evidence that cancers are occurring in excess after people receive COVID-19 vaccinations, according to Dr. Harvey Risch.
Dr. Risch is professor emeritus of epidemiology in the Department of Epidemiology and Public Health at the Yale School of Public Health and Yale School of Medicine. His research has focused extensively on the causes of cancer as well as prevention and early diagnosis.
In an interview for EpochTV’s “American Thought Leaders,” Dr. Risch said patients must now wait months, not weeks, to get an appointment at an oncology clinic in New York.
There is difficulty in observing whether a vaccine can cause cancer, because cancer usually takes time to develop, Dr. Risch said. It can take anywhere from two years to 30 years, depending on the different types of cancer, from leukemia to colon cancer.
“What clinicians have been seeing,” said Dr. Risch, “is very strange things: For example, 25-year-olds with colon cancer, who don’t have family histories of the disease—that’s basically impossible along the known paradigm for how colon cancer works—and other long-latency cancers that they’re seeing in very young people.”
He said this is not how cancer normally develops.
“There has to be some initiating stimulus to why this happens,” he said.
Fighting Cancer
Dr. Risch said that in his opinion, cancer is something a healthy human body can fight and disable, as the non-normal cancerous cells are gobbled up when detected in a body with a functional immune system. If the immune system is compromised, however, it cannot cope with the task of neutralizing cancerous cells, and cancerous cells are left to multiply and grow, leading to symptoms of cancer.
“That’s the mechanism I think is most likely here,” Dr. Risch said. “We know that the COVID vaccines have done various degrees of damage to the immune system in a fraction of people who have taken them.”
That damage could translate to getting COVID more often, getting other infectious diseases, or getting cancer.
Another example Dr. Risch gave was breast cancer, which normally, if there is a remanifestation after surgical removal, the remanifestation occurs after two decades. However, vaccinated women are now seen to remanifest breast cancers in much shorter periods of time.
“Those are the initial signals that we’ve been seeing, and because these cancers have been occurring to people who were too young to get them, basically, compared to the normal way it works, they’ve been designated as turbo cancers,” Dr. Risch said.
“Some of these cancers are so aggressive that between the time that they’re first seen and when they come back for treatment after a few weeks, they’ve grown dramatically compared to what oncologists would have expected for the way cancer normally progresses,” he added.
“Be attuned to your body,” Dr. Risch recommended, for noticing any new signals the body might give.
Adverse Events After Vaccination
Dr. Risch also talked about the aspect of official medical agencies not recognizing someone as being vaccinated inside the first two weeks of vaccination. This happens, he said, because the medical agencies say that the effects of the vaccine need two weeks to start manifesting. Adverse effects occurring a few days after vaccinations were officially counted as health conditions manifesting in unvaccinated people, he said.
However, serious adverse events after receiving the vaccine have occurred within the first four days, Dr. Risch said. He said three-quarters of adverse effects are being recorded as happening to unvaccinated people.
The decision makers who were in charge during the pandemic “threw out the principles of public health six days into the pandemic and did the opposite of everything that we knew should be done for respiratory viruses,” he said.
One example was the denial of effective early treatment and unnecessary vaccinations, which show a “colossal failure of public health through this period,” he said.
Dr. Risch said that a lot of people are now less likely to be “propagandized” regarding COVID, and that news reports about a new variant that is going to take over the world in the next month are “propaganda to sell the next batch of vaccines coming out in a few weeks.”
“People are fed up with this and it’s going to be a lot more pushback,” he said.
Risks to Society
Dr. Risch said that while the individual risk of an adverse reaction to the vaccine is relatively low, once that risk manifests itself at a greater scale, when millions of people have received the vaccine, the result is that hundreds of thousands of people are left with injuries and serious adverse events that are often worse than the virus itself.
Dr. Risch’s opinion is that nobody should get vaccinated with an mRNA vaccine, as the new variants are mild and not life threatening. He has heard of a few hospitalizations that lasted for some days, but as most people had COVID in the past, they have some immunity to these new variants as well.
“There is no reason for people to be vaccinated now, to any degree,” he said.
He said COVID has become an illness similar to the flu in its degree of severity, and that propaganda to scare people is being pushed by the government on behalf of pharmaceutical companies to sell more vaccines.
“We live in social contact with each other and therefore spread low-level infections. This is part of human life that we take for granted and we try to treat it the best we can,” he said. “That’s how we should be managing this.”
Another Covid booster approval using shocking new data has the many turning away for good from the FDA and CDC. Learn the facts about the new COVID-19 shot that was just approved for all Americans over the age of 6 months.
While virtually every US Health Advisor is recommending the new COVID-19 booster for everyone older than 6 months old this Fall, Florida Surgeon General, Dr. Joseph Ladapo, has taken a firm stance to urge healthy people under 65 to NOT get the booster. Hear about the lack of evidence of efficacy and the attacks he has endured from the mainstream media.
It started slowly at first – a trickle of concerning reports that something wasn’t right. In January 2021, just weeks after the rollout of the COVID-19 vaccines, cases of myocarditis began cropping up.
Myocarditis – inflammation of the heart muscle – had never been linked to vaccines before. So when 28 cases were reported to the U.S. vaccine adverse event reporting system (VAERS) [1] that month, it raised eyebrows.
By February, the trickle had become a stream. VAERS received 64 more reports, including two deaths [2]. Then in March, Israel [3] and the military [4] started reporting cases too.
Something strange was going on. But the authorities ignored it.
In March, the FDA authorized the Johnson & Johnson vaccine without a whisper of myocarditis [5]. The CDC soon recommended it for all adults [6]. Colleges and businesses started mandating the shots [7]. It was full speed ahead.
Behind closed doors though, alarm bells were ringing. The CDC met with the military to discuss the myocarditis cases in young troops [8]. Israel was reporting dozens of cases, including in teenagers [9]. The FDA knew from Pfizer that there were nearly 60 cases already in its database [10].
But in public, it was denial and dismissal. The CDC director claimed she wasn’t aware of any military cases [11]. Pfizer hid its database numbers [12]. And the FDA rubber stamped authorization of the Pfizer vaccine for teenagers in May without a mention of myocarditis [13].
As myocarditis reports flooded into VAERS in the hundreds during the summer [14], young, healthy people continued being pressured to get vaccinated. Mandates rolled out across the country [15]. The authorities told the public the benefits outweighed the risks [16].
But patients started sharing their stories of being hospitalized with heart problems after vaccination [17]. Researchers began publishing case reports in medical journals [18]. And still, the CDC publicly downplayed concerns [19].
Behind closed doors, officials strategized about monitoring the alarming reports [20]. They expanded the criteria for identifying myocarditis cases [21]. More hospitals confirmed seeing unusual cases in vaccinated youths [22].
In June, the FDA quietly added warnings about myocarditis to the vaccine fact sheets [23]. The news dripped out slowly that CDC advisers now acknowledged a “likely association” [24].
But the full scope remained obscured. The authorities clung to the narrative that benefits outweighed risks [25]. They used incomplete data and rosy assumptions to claim the vaccines were still worth it for young people [26].
Millions of teenagers continued getting pressured to get vaccinated throughout the summer and fall [27]. It became painfully clear that the drive for widespread vaccination took precedence over transparency and caution.
It wasn’t until October 2021 that the warnings were taken more seriously. Nordic countries limited the Moderna vaccine due to myocarditis concerns [28]. The FDA and CDC were forced to address the risks more openly in meetings [29].
But still, they pushed ahead with expanding the shots to younger ages [30]. Five-year-olds started getting vaccinated in November despite a complete lack of safety data [31]. Booster doses were promoted for teenagers against the advice of their European counterparts [32].
The evidence continued piling up into 2022 that the vaccines were inflaming hearts [33]. Young people, almost all male, were suffering severe outcomes [34]. The FDA fully approved the Moderna and Pfizer vaccines with scarcely a mention of myocarditis [35].
Regulators around the world scaled back recommendations for boosters in young people as more safety signals emerged [36]. But the U.S. charged ahead, even permitting a fourth dose before any trial data was available [37].
Three years and over 1,600 confirmed VAERS reports later [38], the CDC finally admitted publicly that the mRNA vaccines cause myocarditis [39]. But authorities continue maintaining the stance that benefits outweigh risks across all groups [40].
Yet as researchers report finding heart abnormalities months later [41], it’s unclear if the full scope of risks is known. Some experts argue society lost sight of “first, do no harm” in the rush to vaccinate an entire population against COVID-19 [42].
Why were the early warning signs dismissed? How many ended up harmed from ignored or hidden signals [43]? And why does debate about vaccine prudence remain taboo despite mounting evidence condemning overly broad immunization policies [44]?
This story is far from over. As more studies probe long-term effects and deaths possibly caused by vaccine-induced myocarditis [45], questions will continue swirling.
The families forever changed want accountability. Recognition that mass vaccination programs failed to uphold informed consent [46]. And assurances that blindly “following the science” won’t again take precedent over individuals’ health [47].
Myocarditis turned out to be the tip of the iceberg when it came to underestimated vaccine risks [48]. Only time will tell the full scope of lives upended and lost in the race to inoculate the world [49].
Sen. Rand Paul (R-Ky.) on Tuesday for the third time introduced legislation to lift the COVID-19 vaccination requirement for young adults in the U.S. Senate Pages Program — and for the third time, the resolution failed.
The Senate Pages program, which pays young adults ages 16 and 17 to assist on the senate floor, requires applicants be fully vaccinated against COVID-19 — including all boosters.
Paul last week introduced the same resolution but it failed to pass. His first attempt, which also did not pass, was a broader resolution introduced on Sept. 7 that sought to remove COVID-19 testing, vaccination and masking requirements for pages.
A press release issued Wednesday by Paul’s office said Senate Democrats “for the third time” refused to “follow the science” and “unanimously objected” to the resolution.
According to Paul, the requirement is politically motivated, not based on science, and puts healthy American young adults at risk for vaccine-induced myocarditis.
In a senate floor speech before the vote, Rand cited numerous studies that reported an increased risk of heart inflammation with each successive COVID-19 vaccination.
Paul said:
“Why are we forcing these kids to do something that I would say is against medical advice to be a page in our program here?”
“How would you feel if your perfectly-healthy football player or band member is given the vaccine and comes home with heart inflammation?”
Risk of vaccine-related myocarditis is greater than risk of hospitalization from COVID-19
Rand pointed out that a study by epidemiologist Dr. Tracy Beth Høeg, Ph.D., reported the risk of myocarditis in teenage boys after receiving a second dose of an mRNA COVID-19 vaccine was roughly 5 times greater than the risk of hospitalization from COVID-19.
“So you’re asking yourself, ‘Well, can my kid go to the hospital or get the heart inflammation?’” Paul said. Both are rare, he said, but there is a greater chance of heart inflammation.
Paul noted that among healthy children and young adults, there is a “nearly zero” risk of dying from COVID-19.
The public knows this and has “largely resisted” vaccinating their children against COVID-19, he added.
The argument that young people be vaccinated to protect more vulnerable populations does not hold up, Paul said, because “No serious scientist now argues that COVID-19 vaccines stop transmission. No one.”
He added, “Yet here we are, with Democrats saying, ‘You’re not smart enough to make your own decisions. We will make these medical choices for you.’”
‘In a free society, no one should be forced to receive an injection’
Paul called out Democrats for endorsing authoritarianism by expecting “submission” from U.S. parents. He said:
“They don’t want you to have the choice to keep your kids safe and make a decision whether or not your kid, who may well have already had COVID, needs yet another vaccine … They just want you to shut your eyes, be quiet and do as you’re told.”
Paul said the Democrats’ medical policy for citizens is to, “Shut up. Do as you’re told. Take the injection. We don’t care if your kid might get sick. We don’t care if you have a choice. We don’t care if you have any say in your kid’s medical care.”
“In a free society,” he added, “no one should be forced to receive an injection into their body that they do not wish to have.”
Suzanne Burdick, Ph.D., is a reporter and researcher for The Defender based in Fairfield, Iowa. She holds a Ph.D. in Communication Studies from the University of Texas at Austin (2021), and a master’s degree in communication and leadership from Gonzaga University (2015). Her scholarship has been published in Health Communication. She has taught at various academic institutions in the United States and is fluent in Spanish.
My last post presented evidence for what I’ll call the hot lot hypothesis (HLH): the different rates of reported deaths among Covid vaccine batches are due to differences in toxicity, with the earlier batches being especially bad.
But some commenters brought up a legitimate issue with the HLH, which I’ll call the unhealthy vaccinee bias (UVB): the earliest batches were given to the eldest of the elderly and the sickest of the sickly who die at higher rates regardless of what does or doesn’t get injected into them. So hot lots might just be a statistical illusion that goes away once you control for pre-existing health factors, kind of like Covid vaccine effectiveness.
But in Japan, the sick and elderly didn’t get the jabs first; healthcare workers did. In fact, the high-risk elderly only started getting jabbed almost two months after low-risk healthcare workers (February 17th vs April 12th 2021). This is noteworthy not just because it reminds us that the jabs were primarily sold to the population as a way to ‘stop the spread’ but also because it means the earliest batches delivered to Japan went to working-age people, giving us a chance to test the hot lot hypothesis free from the unhealthy vaccinee bias.
And if we were to search for evidence of, say, higher cardiovascular deaths in working-age males, where better to look than the monthly statistics for deaths due to arrhythmia and heart failure rather than just deaths reported after the jabs? The below graphs come yet again from Nagoya University’s Prof Seiji Kojima.
Monthly changes in the number of deaths among men aged 10 to 49 due to arrhythmia from 2018 to 2022
Monthly changes in the number of deaths among men aged 10 to 49 due to heart failure from 2018 to 2022
Did you notice anything odd that happened between February and April 2021? Now, these clear spikes in deaths among men aged 20-49 due to arrhythmia and heart failure don’t necessarily prove the hot lot hypothesis beyond doubt. Maybe the CIA was trying out a new version of its heart attack gun in Japan at the time. But absent any other convincing explanation, I’m going to assume that Pfizer and BioNTech were scraping the bottom of the vat to enable healthcare workers in Japan to roll up their sleeves for their first and second Covid jabs back in early 2021.
Well, any healthcare workers who got lucky in the lot lottery and who’ve kept up to date with their shots will now be able to get the seventh from this week. But not to worry. I’m sure the manufacturers have fixed any and all quality assurance issues they’ve never publicly acknowledged.
The following translation was performed free of charge to protest an injustice: the destruction by the ADL of Ariel Toaff’s Blood Passover on Jewish ritual murder. The author is the son of the Chief Rabbi of Rome, and a professor of Jewish Renaissance and Medieval History at Bar-Ilan University in Israel, just outside Tel Aviv.
Dr. Toaff is uniquely qualified to write this book, being thoroughly familiar with the derivative literature in English, French, German and Italian, as well as the original documentary sources in Latin, Medieval Italian, Hebrew and Yiddish. This is not something he worked on in secret. On the contrary, he worked on it openly with his university students and colleagues in Israel for several years; one of his students was even going to publish a paper on the subject. The author is extremely careful about what he says, and his conclusions must be taken seriously. It reads like a detective story.
If it had been published in Israel, in Hebrew, no one would have cared. There are large bodies of literature in Hebrew that Jews do not wish Gentiles to know about. But Dr. Toaff’s announcement of its publication in Italy, in Italian, raised a worldwide firestorm of fury.
Under unbearable pressure, the book was withdrawn from publication. Come in out of the darkness, and strike a blow for the light.
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Some UK military personnel and their families have been turning to food banks because of the increasing pressures from the cost of living crisis, a British news network has reported.
Monthly changes in the number of deaths among men aged 10 to 49 due to arrhythmia from 2018 to 2022
Monthly changes in the number of deaths among men aged 10 to 49 due to heart failure from 2018 to 2022
The following translation was performed free of charge to protest an injustice: the destruction by the ADL of Ariel Toaff’s Blood Passover on Jewish ritual murder. The author is the son of the Chief Rabbi of Rome, and a professor of Jewish Renaissance and Medieval History at Bar-Ilan University in Israel, just outside Tel Aviv.
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