By Rebecca Weisser

That’s a more radical decision than it might sound, but what he, and others, are finding is disturbing.

According to Sasha Latypova, a scientist with 25 years of experience in clinical trials for pharmaceutical companies, the contract between Pfizer and the US government prohibits independent researchers from studying the vaccines.

They claim it would ‘divert’ these precious resources away from their intended use fulfilling an ‘urgent’ need.

Is that true in Australia? Who knows? All the Commonwealth Department of Health has said about its contract with Pfizer is that it is commercial-in-confidence.

The Therapeutic Goods Administration performs tests on all Covid vaccines for composition and strength, purity and integrity, identity and endotoxins, but it provides scant details other than the batch numbers tested and whether they passed. (Spoiler alert: they did.)

In the US, the Centers for Disease Control specifically states that all Covid-19 vaccines are free from ‘metals, such as iron, nickel, cobalt, lithium, and rare earth alloys’ and ‘manufactured products such as micro-electronics, electrodes, carbon nanotubes, and nanowire semiconductors’.

Notably, this list does not include graphene oxide which has been widely investigated for biomedical applications. Some researchers sing its praises, its ‘ultra-high drug-loading efficiency due to the wide surface area’, its exceptional ‘chemical and mechanical constancy, sublime conductivity and excellent biocompatibility’.

But there’s a catch. ‘The toxic effect of graphene oxide on living cells and organs’ is ‘a limiting factor’ on its use in the medicine.

So is there graphene oxide in the Pfizer shots?

What Nixon found, and filmed, is bizarre to say the least. Inside a droplet of vaccine are strange mechanical structures.

They seem motionless at first but when Nixon used time-lapse photography to condense 48 hours of footage into two minutes, it showed what appear to be mechanical arms assembling and disassembling glowing rectangular structures that look like circuitry and micro chips.

These are not ‘manufactured products’ in the CDC’s words because they construct and deconstruct themselves but the formation of the crystals seems to be stimulated by electromagnetic radiation and stops when the slide with the vaccine is shielded by a Faraday bag.

Nixon’s findings are similar to those of teams in New Zealand, Germany, Spain and South Korea.

An Italian group led by Riccardo Benzi Cipelli analysed the blood of over 1,000 people, one month after they were vaccinated, who had been referred for tests because they had experienced side effects.

They ranged in age from 15 to 85 and had had between one and three doses. More than 94 per cent had abnormal readings, deformed red blood cells, reduced in counts and clumped around luminescent foreign objects which also attracted clusters of fibrin.

Some of the foreign objects dotted the blood like a starry night, some self-assembled into crystalline structures and others into spindly branches and tubes.

The Italians think the objects are metallic particles and say they resemble ‘graphene oxide and possibly other metallic compounds’.

They believe the damaged blood is contributing to post-vaccine coagulation disorders, which in turn contribute to increased malignancies, while graphene-family materials are associated with oxidative stress, DNA damage, inflammation and damage to those parts of the immune system that suppress tumours.

The artificial mRNA concoction which is ‘cloaked’ from the recipient’s immune system is also likely to reduce the recipients immune function, increasing the likelihood of new or recurring tumours.

Nixon has shared his findings with Wendy Hoy, professor of medicine at the University of Queensland who has called on the Australian government and its health authorities to explain the apparent spontaneous formation of chips and circuitry in mRNA vaccines when left at room temperature, and the abnormal objects that can be seen in the blood of vaccinated people.

Hoy thinks that these are ‘undoubtedly contributing to poor oxygen delivery to tissues and clotting events, including heart attacks and strokes’ and asks why there is no systematic autopsy investigation of deaths to investigate the role of the vaccine in Australia’s dramatic rise in mortality.

According to the latest data from the Australian Bureau of Statistics, excess mortality was over 17 percent in July. It is similarly elevated in other highly vaccinated populations.

In Germany, excess mortality in people over 60 increased by 174 percent between 20 September 2021, when 85 per cent of people over 60 were fully vaccinated, and October 2022.

In the UK, there have been more excess deaths in the last three months than at any time during the pandemic or indeed since 2010. In the most recent week, excess mortality in England was 16 percent.

In the US, excess mortality in people aged 25 to 44, and in those aged 75 to 84, is 18 per cent, and it is 15 percent in those aged 65 to 74.

The situation is all the more alarming because there should be fewer deaths now.

There has also been a dramatic rise in people with disabilities.

As for Covid, in Australia, vaccine efficacy appears to be negative, judging by the statistics in NSW which are far from perfect but the best in Australia.

They show that 88 per cent of people who died were vaccinated even though they made up only 85.5 per cent of the population. They also showed that the unvaccinated made up only 0.15 per cent of people in hospital with Covid and only 1.1 per cent of people in ICU.

Why is this? Almost certainly, because the unvaccinated who die of Covid in NSW are frail and elderly with multiple comorbidities, living in aged care or palliative care or at home, and don’t go to hospital.

Why weren’t they vaccinated? Probably because they or their doctors feared it would kill them.

The question is, how many others is it killing too?

Until health authorities tell us what’s in the shots, we won’t know.

Source: Principia Scientific International & Spectator

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By Will Jones

New evidence has emerged that the mRNA COVID-19 vaccines are routinely injuring the heart of all vaccine recipients, raising further questions about their safety and their role in the recent elevated levels of heart-related deaths. 

The latest evidence comes in a study from Switzerland, which found elevated troponin levels – indicating heart injury – across all vaccinated people, with 2.8% showing levels associated with subclinical myocarditis.

The official line on elevated heart injuries and deaths, where they are acknowledged, is that they are most likely caused by the virus as a post-Covid condition rather than the vaccines.

However, expert group HART (Health Advisory and Recovery Team) has pointed to Australia as a “control group” on this question. HART notes that even though Australia had not had significant Covid (only 30,000 reported infections and 910 deaths) prior to mid-2021, it still saw a trend in excess non-Covid deaths beginning in June 2021 (see below). HART notes that Australia “did not have prior Covid as a reason for seeing this rise in mortality and hospital pressure from spring 2021”. Instead, “the results from this control group indicate that the cause of this rise in deaths, particularly in young people, must be something in common with Australia, Europe and the USA”.

In New Zealand, economist John Gibson found a temporal association between boosters and excess deaths, estimating “16 excess deaths per 100,000 booster doses” (see below). He noted that the age distribution of the deaths corroborated the hypothesis: “The age groups most likely to use boosters show large rises in excess mortality after boosters are rolled out.”

In Japan, Guy Gin reports that Professor Seiji Kojima of Nagoya University found the same correlation during the booster rollout in January to March 2022 (see below) – a time when most excess deaths were not with Covid.

In Israel, a study in Nature observed a similar trend for 16-39 year-olds, with cardiac arrest emergency calls rising and falling with the first and second doses and then rising and falling again after doses for recovered individuals.

Dr. Eyal Shahar looked at the Israeli deaths data for all ages and estimated “a plausible range of the booster fatality rate in Israel in August 2021” of eight to 17 deaths per 100,000 vaccinees. In the Netherlands, vaccinologist Dr. Theo Schetters estimated a booster fatality rate in the over-60s as high as 125 per 100,000 vaccinees. 

As to cause, Dr. Michael Palmer and Dr. Sucharit Bhakdi at Doctors for Covid Ethics have set out what they deem “irrefutable proof of causality” that mRNA vaccines are causing vascular and organ damage. From studies and autopsy evidence the medical experts show:

1. mRNA vaccines don’t stay at the injection site but instead travel throughout the body and accumulate in various organs;
2. mRNA-based Covid vaccines induce long-lasting expression of the SARS-CoV-2 spike protein in many organs;
3. Vaccine-induced expression of the spike protein induces autoimmune-like inflammation;
4. Vaccine-induced inflammation can cause grave organ damage, especially in vessels, sometimes with deadly outcome.

They explain that autopsy evidence shows that “the strong expression of spike protein in heart muscle after vaccination correlates with significant inflammation and tissue destruction”. They add that “vaccine-induced vascular damage will promote blood clotting, and clotting-related diseases such as heart attack, stroke, lung embolism are very common in the adverse events databases”.

A recent case report in Vaccines of an autopsy conducted on a 76-year-old man who died three weeks after receiving his third COVID-19 vaccination confirms the role of the vaccine. It found the presence of spike protein but not the nucleocapsid protein in the deceased man’s brain and heart, proving that the vaccine (which unlike the virus only produces the spike protein) was the cause of the deadly inflammation.

In the heart, signs of chronic cardiomyopathy as well as mild acute lympho-histiocytic myocarditis and vasculitis were present. Although there was no history of COVID-19 for this patient, immunohistochemistry for SARS-CoV-2 antigens (spike and nucleocapsid proteins) was performed. Surprisingly, only spike protein but no nucleocapsid protein could be detected within the foci of inflammation in both the brain and the heart, particularly in the endothelial cells of small blood vessels. Since no nucleocapsid protein could be detected, the presence of spike protein must be ascribed to vaccination rather than to viral infection. The findings corroborate previous reports of encephalitis and myocarditis caused by gene-based COVID-19 vaccines.

A case report of the autopsy of a 55-year-old patient who died four months after receiving a Pfizer jab as a second dose (his first dose was AstraZeneca) made similar findings.

SARS-CoV-2 Spike protein, but not nucleocapsid protein was sporadically detected in vessel walls by immunohistochemical assay. The cause of death was determined to be acute myocardial infarction and lymphocytic myocarditis. These findings indicate that myocarditis, as well as thrombo-embolic events following injection of spike-inducing gene-based vaccines, are causally associated with a injurious immunological response to the encoded agent.

A recent meta-analysis claimed to find that the risk of myocarditis is “more than seven fold higher in persons who were infected with the SARS-CoV-2 than in those who received the vaccine”. It claims this supports “the continued use of mRNA COVID-19 vaccines among all eligible persons per CDC and WHO recommendations”.

However, critics have pointed out the numerous flaws in this meta-analysis and highlighted that it is at odds with a major Nordic study of 23 million people that found the risk of hospitalisation post-vaccination in 16-24 year old males was up to 28 times higher than the risk post-Covid. At the Daily Sceptic we have written about this Nordic study as well as a number of other studies with similar findings, including ones from France, England and the U.S. (alongside critiques of studies that purport to show otherwise). A study from Israel confirms the elevated risk from vaccination and states: “We did not observe an increased incidence of neither pericarditis nor myocarditis in adult patients recovering from COVID-19 infection.” A study from Italy found a similar absence of elevated myocarditis during the pre-vaccination pandemic period.

We should also note that vaccination does not prevent Covid infection so the risks are additive and the comparison between vaccination risk and infection risk is false. Cardiovascular injury also is not the only serious adverse event associated with these vaccines. A recent study by researchers from Harvard, Oxford and Johns Hopkins University (among others) found that the mRNA vaccines are up to nearly 100 times more likely to cause a person of student age serious injury than prevent him or her from being hospitalised with COVID-19.

Most of these studies only look at clinical adverse events, i.e., events serious enough to warrant medical assistance. Studies are now emerging which show these clinical events to be just the tip of the iceberg of a far larger number of subclinical injuries. A study in Thailand found cardiovascular adverse effects in around a third of teenagers (29.2%) following Pfizer vaccination and subclinical heart inflammation in one in 43 (2.3%).

The Swiss study mentioned above was recently highlighted by Dr. Vinay Prasad and comes from the European Society of Cardiology. It confirms the Thai result, finding at least 2.8% with subclinical myocarditis (possibly more as the researchers excluded half the cases as possibly from another cause). Dr. Prasad observes that this means subclinical myocarditis is hundreds of times (“two orders of magnitude”) more common than clinical myocarditis. The rates were highest in women at 3.7%, which is one in 27 vaccinated. (Dr. Prasad notes this is different to the Thai study, which found the usual higher rates in males; he suggests this may be related to how the researchers excluded cases.)

Crucially, the study found elevated troponin levels – indicating heart injury – across all vaccinated people (see chart above, where the dark lines being shifted to the right of the fainter control group lines implies elevated levels throughout the vaccinated population). This indicates the vaccine is routinely injuring the heart (an organ which does not heal well) and that the known injuries are just the more severe instances of a far larger number occurring right across the board.

These injuries are not necessarily short and over with quickly. Studies have shown that spike protein is still being found in the blood of many vaccinated people at least four months after vaccination, suggesting it is still being produced in some way. The mechanism of this long-term production of spike protein by the body has not been identified (is the genetic code being incorporated into the cell’s DNA?). But if cells in the cardiovascular system and elsewhere are still producing this pathogenic and inflammatory protein for months on end, the risk of auto-immune injury as identified in the autopsies above greatly increases. Such an auto-immune injury may be triggered by re-challenge by the virus ramping up the immune response to the spike protein, which may explain why excess non-Covid deaths often accompany Covid waves.

There is now considerable evidence that mRNA vaccines are routinely injuring the heart, with raised troponin levels across the board and subclinical myocarditis in up to one in 27 cases or more. These are not rare events, as is often claimed by medical authorities and in the media. They are alarmingly common.

Source: The Daily Sceptic

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