Do you remember back during the Planscamdemic when Dr. Charles Lieber of Harvard University’s chemistry department was arrested for not disclosing financial relationships with…(cough)… laboratories in China? Do you also remember when it was revealed that his “specialty” was revealed to be how to use nano-particles and how they might in turn be used to carry drugs into the brain past the blood-brain barrier? And do you remember who that touched off an internet scramble to investigate all the implications of nano-particles and covid mRNA injections, and how people quickly found patents by Baal Gates who wanted to create an “updatable” quackcine technology that you wore in your body, and updated like those never-welcome-take-forever Windows updates? Remember how some people speculated that to make such a technology work, it would have to be via nano-particles being implanted somehow in the body (hmmm…. I wonder how?), particles which in turn would respond to certain types of electromagnetic signals contituting the “update” from the quackcine company? (For convenience’s sake, let’s call that company Microcrud-Nanoshinola LLC). Do you remember when some started drawing connections between all of this and the quackcines and the adverse reactions? Remember how The Science and The Media said that making connections between all of this – the planscamdemic, the arrest of Lieber, the patents and quackcine schemes of Baal Gates – were all kooky conspiracy theorists/
Well… two doctors in Korea are confirming at least part of this scenario according to the following article shared by V.T. (with our thanks):
Confirming what many suspected to be the case, two Korean scientists have found that the mRNA vaccine vials from both Pfizer-BioNTech and Moderna contain self-assembling nanoparticles that form into the white clots that many embalmers are discovering inside the bodies of the “fully vaccinated.”
The findings of these two scientists closely resemble what Mike Adams, the Health Ranger, found when he reported on these embalmer clots back in January 2022. (Be sure to check out this report highlighting the footlong clots found in some fully vaccinated dead bodies.)
What Adams apparently found concerning these clots is that they are not composed of actual human tissue, nor do they contain amyloid proteins, according to Dr. Ruby – so what are they, exactly?
If that’s the case, then what of the mechanism for the update from Microcrud-Nanoshinola LLC? What is interesting to me is that this article actually goes there; what was “conspiracy theory” a few short years ago is now a possibility that is being considered:
The clots in question apparently contain magnetic graphene that grows in both arteries and veins. In some cases, the resulting clot is upwards of three feet in length and could be used as an antenna system for WiFi signals to connect the fully jabbed to “the borg.”
“Can you hear a high pitch frequency that increases in amplitude at night?” the X account that reiterated all of this asked of Dr. Ruby, who confirmed that she is aware of this having “broke the worldwide story of La Quinta Columna and the graphene oxide as well as the first embalmer report.”
The real question left unanswered by the article’s high octane speculation is why would one want to inject such nano-particles into someone for the purposes of Wifi signal reception, when the injection only causes the people receiving them to die? What use is a dead antenna? Is it, as the appended video in the article suggests, to somehow create “zombies”, a “fake general resurrection” by creating massive nervous reactions in dead people via strong electromagnetic pulse? (It sounds crazy, I know, but then again, these people are bat-shinola crazy.) Perhaps, perhaps not. What is intriguing here is the apparent discovery of graphene and other metals in some of the injections, which can act as antenna.
I find all this intriguing because I have a friend with Morgellon’s disease, remember that one? This was a strange disease that some people began to report during the 1990s and early 2000s. We were assured by The Science and The Media that there was no such disease and that it was just all some sort of mass hypercondria. But what many of these people reported was a sensation of tingling, like ants crawling under their skin. They reported lesions, and these in turn would be focuses for the feeling that insects were crawling under their skin. Some reported being particularly sensitive to increased electromagnetic background noise. Then in my friend’s and a few other people’s cases, a physician, Dr. Hildegard Stavanger, stepped forward to actually investigate – that’s called science, folks, as distinct from The Science – and what she discovered was nothing less than amazing: tiny “plastic” nano-fibers, many of them growing in the lesions of her patients. These in turn acted like tiny nano-antennae, and when electromagnetic background radiation increased, sure enough, the Morgellon’s victims’ pain increased. Many, as a result of these early findings, speculated that the nano-fibers were entering the bodies of the victims through the so-called “chemtrail” spraying that many alleged was going on. Others looked to genetically modified foods. The latter may seem an even more unlikely candidate, but it should be remembered that in the wake of quackcine skepticism during the planscamdemic, it was alleged that members of the Technokookracy including Baal Gates advocated putting the quackcines into the GMOs, and with that, the nano-particles, GMO foods, and whatever sick and twisted agenda was behind all of this, linked up again. The story about Gates, so we’re told, was false:
What’s interesting, however, is that the basic conceptual point is not denied by the “fact check” in that vaccine-via-food is an admitted research goal:
Uh huh. Just like no program of nano-particles was being studied here by Dr. Lieber, either. And as for genes crossing into other species, check this out:
My point here is that all of this high octane dot-connecting is not implausible.
All of this brings us to the real question squatting like a big fat ugly toad in the middle of all this swirling cloud of disconnected dots: who is poisoning us, and why? It seems evident to anyone with a real brain who is not leaping onto the propaganda bandwagon of The Science and The Media, that someone very much wants us dead; our food supply is poison, our drugs are poison, our “vaccines” have been redefined so that hugely experimental injections can be called vaccines and tested on human populations under the guise of a “health emergency”, and many people taking those “safe and effective” injections are suffering, or have died, in cruel fashions. And The Media and The Science are silent (and The Science is enjoying a well-paid retirement, apparently). So… again… who wants us dead so badly, and why? I have a few ideas, but I’d like to hear yours.
But whatever we make of it, some doctors in some countries haven’t entirely lost their minds, and are willing to say what needs to be said. Shame on all the big networks of the American propataintment media for not even bothering with the story.
See you on the flip side…
(If you enjoyed today’s blog, please share it with your friends.)
Researchers Call for Urgent Action to Address Mass Contamination of Blood Supply
May 27, 2024
STORY AT-A-GLANCE
Japanese researchers warn of the risks of using blood from mRNA COVID vaccine recipients, highlighting potential deadly effects and the need for urgent action to secure the global blood supply
Blood contaminated with prion-like structures from the spike protein raises the risk of inducing fatal neurodegenerative diseases in recipients. The potential transmission of harmful proteins through exosomes (“shedding”) and the risk of autoimmune diseases due to the vaccines’ mechanism and components like lipid nanoparticles (LNPs) are other major concerns
Proposals for managing blood collection include rigorous donor interviews, deferral periods, and a suite of tests to ensure the safety of blood products
The researchers advocate for comprehensive testing of both jabbed and unjabbed individuals to assess the safety of blood products and suggest discarding blood products contaminated with spike proteins or modified mRNA until effective removal methods have been developed
They call for suspending all gene-based “vaccines” and conducting a rigorous harm-benefit assessment in light of the serious health injuries reported. They also urge countries and organizations to take concrete steps to address and mitigate the already identified risks
In a recent meta-analysis1,2 posted on preprints.org, Japanese researchers warn of potentially deadly risks to patients who receive blood from people who have taken mRNA COVID jabs and call for urgent action to ensure the safety of the global blood supply. According to the authors:3
“… many countries around the world have reported that so-called genetic vaccines, such as those using modified mRNA encoding the spike protein and lipid nanoparticles as the drug delivery system, have resulted in post-vaccination thrombosis and subsequent cardiovascular damage, as well as a wide variety of diseases involving all organs and systems, including the nervous system …
[B]ased on these circumstances and the volume of evidence that has recently come to light, we call the attention of medical professionals to the various risks associated with blood transfusions using blood products derived from people who have suffered from long COVID and from genetic vaccine recipients, including those who have received mRNA vaccines, and we make proposals regarding specific tests, testing methods, and regulations to deal with these risks.”
Blood From Jabbed Donors May Pose Risk to Neurological Health
One particular risk addressed in this paper is the implications of blood tainted with prion-like structures found within the spike protein. Prions are misfolded proteins that can cause neurodegenerative diseases, such as Creutzfeldt-Jakob Disease (CJD) in humans, by inducing the misfolding of normal proteins in the brain.
Prion diseases are characterized by a long incubation period, followed by rapid progression and high mortality. The suggestion that the spike protein of SARS-CoV-2, especially from certain variants, might contain prion-like domains raises concerns for several reasons:
Transmission risk — If spike proteins with prion-like structures can be transmitted through blood transfusions, there might be a risk of inducing prion diseases in recipients. Prion diseases are notoriously difficult to diagnose early, have no cure, and are fatal, making any potential transmission through blood products a significant safety concern.
Detection and removal challenges — Current blood screening processes do not specifically test for prions, partly because prion diseases are rare and partly due to the technical challenges in detecting prions at low concentrations. If spike proteins with prion-like properties are present in the blood of COVID jabbed individuals, existing blood safety protocols may not be adequate to prevent transmission.
Long-term safety concerns — Prion diseases have long latency periods, meaning that symptoms can appear years or even decades after exposure. This delay complicates efforts to trace the source of an infection back to a blood transfusion and assess the safety of blood supplies over time.
Impacts on blood supply management — Concerns about the potential risks associated with prion-like structures in spike proteins might lead to changes in donor eligibility criteria or the implementation of additional screening measures. These changes could impact the availability of blood products, which are critical for routine medical procedures.
Public confidence — Public awareness of these potential risks, even if they are theoretical or have a very low likelihood of occurring, could affect individuals’ willingness to donate or receive blood transfusions, thereby lowering blood donation rates and the overall trust in the safety of blood transfusions.
The authors stress the need for comprehensive studies to better understand the implications of these prion-like structures in the spike protein, not only for mRNA jab safety but also for the broader implications for public health measures like blood transfusion practices.
Other Potential Health Hazards of Contaminated Blood
Contaminated blood may also pose other serious health risks, including:
•Reduced immune function among blood recipients — It’s been shown that the more doses of the COVID shot you’ve received, the more likely you are to suffer future infections, either by SARS-CoV-2 or other viruses, due antibody-dependent enhancement.
Blood donations from people who have received several doses of mRNA injections may not provide adequate immunity against common infections, resulting in subclinical infections and diseases in recipients.
•Formation of blood clots and amyloid aggregates — If the immune system of a blood recipient isn’t strong enough to neutralize spike protein, blood clots and amyloid aggregates may also form.
•Chronic inflammation — Prolonged exposure to the antigens from the COVID-19 shots can trigger the generation of IgG4 antibodies, resulting in chronic inflammation and immune dysfunction.
IgG4 antibodies are often associated with chronic exposure to antigens, such as those seen in persistent infections, certain cancers, and prolonged exposure to allergens. IgG4 antibodies are also associated with a unique condition known as IgG4-Related Disease (IgG4-RD), a fibro-inflammatory condition characterized by swellings or masses in affected organs.4
Blood Transfusions and the Risk of Autoimmune Diseases
The authors also raise concerns about the potential of contaminated blood to cause autoimmune diseases in recipients. Recent research found that the RNA pseudouridylation, a process in which uracil is swapped out for synthetic methylpseudouridine, can cause frameshifting, basically a glitch in the decoding, which can trigger the production of off-target aberrant proteins.
The antibodies that develop as a result may, in turn, trigger off-target immune reactions. In addition to that, lipid nanoparticles (LNPs), a key component of the COVID shots, have been identified as highly inflammatory and possessing more potent adjuvant activity compared to traditional vaccine adjuvants, which further increases the risk of an autoimmune response. As reported in the featured paper:5
“Recent studies have shown that RNA pseudouridylation can result in frameshifting. It is not yet clear whether a portion of the pseudouridinated mRNA for the spike protein is translated into another protein of unknown function in vaccine recipients. If these proteins are also pathogenic, additional testing for such frameshift proteins may be needed in the future.
Even if a frameshift protein is not toxic, it must be foreign to the body and could cause autoimmune disease. In addition, LNPs themselves are highly inflammatory substances … LNPs have been found to have stronger adjuvant activity than the adjuvants used in conventional vaccines, and there is also concern about autoimmune diseases resulting from this aspect.
Thus, although it is not clear what the causative agent of autoimmune disease is, the large number of reported cases of autoimmune disease following genetic vaccination is extremely concerning.
The very mechanism of gene vaccines that causes one’s own cells to produce the antigens of pathogens carries the risk of inducing autoimmune diseases, which cannot be completely avoided even if mRNA pseudouridylation technology is used.
In this context, individuals with a positive blood test for spike protein may need to have interviews and additional tests for autoimmune disease indicators, such as antinuclear antibodies.
Alternatively, if the amino acid sequence of the protein resulting from the frameshift is predictable, these candidate proteins could be included in the initial mass spectrometry assay. In any case, it is particularly important to develop tests and establish medical care settings in anticipation of these situations.”
Proposals for Managing Blood Collection
The authors outline several specific proposals for managing blood collection and blood products from individuals who have received genetic “vaccines.” Given the variety of blood-related abnormalities observed post-jab, the researchers argue that rigorous and precautionary measures in blood handling and transfusion practices have now become a necessity.
A key part of the proposal involves conducting thorough interviews with potential blood donors. These interviews should cover their vaccination status, number of doses received, their COVID-19 infection history, and any symptoms they might be experiencing that could indicate conditions like post-vaccination syndrome (PVS), long-COVID or other complications.
The researchers also recommend deferral periods for blood collected from COVID jab recipients — 48 hours for mRNA shots and six weeks for AstraZeneca DNA jab recipients. A series of tests are also proposed to ensure the safety of collected blood, including:
Mass spectrometry to measure spike protein content
PCR for detecting the presence of spike protein mRNA and DNA
Testing for markers associated with autoimmune disorders
Enzyme-linked immunosorbent assay (ELISA)
Immunophenotyping
Liquid biopsies combined with proteomics to detect and quantify spike protein and its mRNA
The authors also note that policies and procedures must be constantly revised as new risks and problems with blood products derived from mRNA and DNA jab recipients are identified.
Ensuring Safety of Current Blood Products
The paper also reviews strategies to ensure the safety of blood products already collected, highlighting the complex challenges that medical institutions, regulatory bodies, and the broader healthcare ecosystem must navigate in the wake of widespread use of mRNA injections.
The primary concern is the risk posed to patients by the use of blood products from donors who have received gene-based injections without confirming the presence or absence of spike proteins or modified mRNA. To ensure their safety, methods to quantify potential contaminants must be developed and implemented as soon as possible.
Another critical issue that must be addressed is the current lack of reliable methods to remove spike proteins or modified mRNA from blood products. The authors warn that, given the potential persistence, low solubility, heat resistance, and radiation resistance of these components, current methodologies are inadequate for the job. The only solution, they say, is to discard all blood products found to contain these contaminants until effective removal techniques are established.
Researchers Call for Widespread Blood Testing
Additionally, the researchers call for widespread testing of both jabbed and unjabbed to assess the potential transmission of spike proteins through exosomes (so-called shedding).
As noted by the authors:
“… when exosomes collected from vaccine recipients were administered to mice that had not been vaccinated with the genetic vaccine, the spike protein was transmitted.
Therefore, it cannot be denied that the spike protein and its modified genes can be transmitted through exosomes. For this reason, we suggest that full testing be done initially, regardless of genetic vaccination status, and that a cohort study be conducted to quickly capture the full picture …
In addition … it cannot be ruled out that even those who have not been vaccinated with the genetic vaccine, but have had long COVID, may have residual spike proteins or fibrin- derived microthrombi in their bodies, so it would be advisable to conduct the same testing and follow-up as for genetic vaccine recipients.
The presence or absence and amount of anti-nucleocapsid antibodies as well as antibody isotypes may be an indicator(s) in distinguishing whether genetic vaccination or long COVID is the cause. In any case, these cohort studies are expected to help establish cutoff values for blood levels of spike protein and other substances to determine the safety of blood products.
Faksova et al. conducted a large cohort study of 99 million people using a multinational Global Vaccine Data NetworkTM (GVDN®) and found a significantly increased risk of myocarditis, pericarditis, Guillain-Barre syndrome, and cerebral venous sinus thrombosis in genetic vaccine recipients.”
Ensuring the traceability of blood products and establishing a rigorous legal and regulatory framework to manage the myriad issues arising from the use of blood products derived from COVID jabbed individuals are also paramount. This includes creating systems for the registration of all potential donors, ensuring the traceability of blood products, and conducting recipient outcome studies.
Call to Pause: Evaluating the Risks and Benefits of Genetic Vaccines for a Safer Future
In conclusion, the authors point out that if we continue using mRNA-LPN-based platforms to replace conventional vaccines or create new ones, then the risks to our blood and bone marrow supply will be augmented further.
“The impact of these genetic vaccines on blood products and the actual damage caused by them are unknown at present,” they write.6
“Therefore, in order to avoid these risks and prevent further expansion of blood contamination and complication of the situation, we strongly request that the vaccination campaign using genetic vaccines be suspended and that a harm-benefit assessment be carried out as early as possible, as called for by Fraiman et al.7 and Polykretis et al.8
[T]he health injuries caused by genetic vaccination are already extremely serious, and it is high time that countries and relevant organizations take concrete steps together to identify the risks and to control and resolve them.”
Mounting research suggests a serious side effect of the COVID mRNA jabs could be dementia, and the prions that cause it may be contagious
Frameshifting, as we now know occurs in the COVID shots, can induce prion production and lead to neurodegenerative diseases such as Alzheimer’s and Creutzfeldt-Jakob disease (CJD)
Sid Belzberg’s prions.rip website, which collected data on neurological side effects post-jab, found a notably high incidence of diagnosed CJD cases, suggesting an alarming trend
A series of articles highlight biases in clinical trials and observational studies, suggesting COVID-19 vaccines’ safety and effectiveness have been massively overstated
The Global COVID Vaccine Safety Project study — funded by the U.S. Centers for Disease Control and Prevention — reveals significant side effects, including myocarditis, pericarditis, and blood clots, underscoring the need for reevaluation of COVID vaccine risks and benefits
According to mounting data, one of the more serious side effects of the COVID mRNA jabs appears to be dementia, and worse yet, this previously untransmissible disease may now be “contagious,” transmissible by way of prions.
In my 2021 interview with Stephanie Seneff, Ph.D., she explained why she suspected the COVID shots may eventually result in an avalanche of neurological prion-based diseases such as Alzheimer’s. She also published a paper detailing those mechanisms in the May 10, 2021, issue of the International Journal of Vaccine Theory. As she explained in that paper:1
“A paper published by J. Bart Classen (2021) proposed that the spike protein in the mRNA vaccines could cause prion-like diseases, in part through its ability to bind to many known proteins and induce their misfolding into potential prions.
Idrees and Kumar (2021) have proposed that the spike protein’s S1 component is prone to act as a functional amyloid and form toxic aggregates … and can ultimately lead to neurodegeneration.”
In summary, the take-home from Seneff’s paper is that the COVID shots, offered to hundreds of millions of people, are instruction sets for your body to make a toxic protein that will eventually wind up concentrated in your spleen, from where prion-like protein instructions will be sent out, leading to neurodegenerative diseases.
What Are Prions?
The term “prion” derives from “proteinaceous infectious particle.” Prions are known to cause a variety of neurodegenerative diseases in animals and humans, such as Creutzfeldt-Jakob disease (CJD) in humans, bovine spongiform encephalopathy (BSE or “mad cow disease”) in cattle, and chronic wasting disease in deer and elk.
These diseases are collectively referred to as transmissible spongiform encephalopathies (TSEs). They’re characterized by long incubation periods, brain damage, the formation of holes in the brain giving it a sponge-like appearance, and failure to induce an inflammatory response.
In short, prions are infectious agents composed entirely of a protein material that can fold in multiple, structurally distinct ways, at least one of which is transmissible to other prion proteins, leading to a disease that is similar to viral infections but without nucleic acids.
Unlike bacteria, viruses, and fungi, which contain nucleic acids (DNA or RNA) that instruct their replication, prions propagate by transmitting their misfolded protein state to normal variants of the same protein.
According to the prion disease model, the infectious properties of prions are due to the ability of the abnormal protein to convert the normal version of the protein into the misfolded form, thereby setting off a chain reaction that progressively damages the nervous system.
Prions are remarkably resistant to conventional methods of sterilization and can survive extreme conditions that would normally destroy nucleic acids or other pathogens, which is part of why prion diseases are so difficult to treat.
More Evidence mRNA Shots Can Trigger Dementia
Today, there’s even more evidence to support Seneff’s theory. In August 2022, tech entrepreneur Sid Belzberg wrote2 about prions.rip, a website he’d set up to collect data on the neurological side effects of the jabs. (This site is no longer live.)
Within a few months, the site had received about 15,000 hits and gathered 60 reports from people who got the jab and suffered neurological deficits shortly thereafter, including six cases of diagnosed CJD.
“Normally this disease affects 1 in a 1,000,000 people,” Belzberg wrote.3“To get 6 cases you would need 6,000,000 hits to the site assuming everyone reports. The chances of getting 1 case in 15,000 hits is 1 in 66. To see 6 cases in 1 group of 15,000 is 1/66^6 or 1 in 82,000,000,000, or 20 times more likely to win a Powerball lottery! …
To reiterate, CJD is an exceptionally rare disease that is now a known and established severe adverse reaction (SAE) from the DEATHVAX™. Injecting this slow kill bioweapon can cause ailments that are about as likely to develop in the real word as getting struck by lightning twice. The proof is now irrefutable.”
Frameshifting Can Result in Prion Production
In mid-December 2023, researchers reported4,5,6 that the replacing of uracil with synthetic methylpseudouridine in the COVID shots — a process known as codon optimization — can cause frameshifting, a glitch in the decoding, thereby triggering the production of off-target aberrant proteins.
The antibodies that develop as a result may, in turn, trigger off-target immune reactions. According to the authors, off-target cellular immune responses occur in 25% to 30% of people who have received the COVID shot. But that’s not all.
According to British neuroscientist Dr. Kevin McCairn, this frameshifting phenomenon has also been linked to harmful prion production — and that frame shifted prions, specifically, are infectious and can be transmitted from one person to another. As reported in the Journal of Theoretical Biology in 2013:7
“A quantitatively consistent explanation for the titres of infectivity found in a variety of prion-containing preparations is provided on the basis that the etiological agents of transmissible spongiform encephalopathy comprise a very small population fraction of prion protein (PrP) variants, which contain frameshifted elements in their N-terminal octapeptide-repeat regions …
Frameshifting accounts quantitatively for the etiology of prion disease. One per million frameshifted prions may be enough to cause disease. The HIV TAR-like element in the PRNP mRNA is likely an effector of frameshifting.”
McCairn explained this mechanism in a February 19, 2023, interview with Health Alliance Australia (video above). In it, he noted:
“Mis-folded proteins caused by prions can impact every level organ and tissue system in the body … [They] bioaccumulate and are resistant to degradation, thereby building up …”
Prions may in fact be the primary molecule that is being “shed” by COVID jab recipients, and if those prions are due to frameshifting, that could be very bad news indeed, considering their implication in dementia.
Another doctor who believes we’ll be facing an “epidemic of prion disease” is Dr. David Cartland. In late February 2024, he posted8 13 scientific papers linking the COVID jabs, prion diseases and CJD, noting that was just a “small selection” of what’s available in the medical literature.
Prions Implicated in Long COVID as Well
According to genomics expert Kevin McKernan, Ph.D., prions are also involved in long COVID (or as McKernan calls it, “long vax”).9 In one 2024 study,10 96.7% of long COVID sufferers had received the jab. In an interview with the Front Line COVID-19 Critical Care Alliance (FLCCC), McKernan stated:11
“If you frameshift over the stop codons, you’re going to be making proteins that are spike-mito proteins. When I talk to a lot of the long vax patients I hear of all these things that remind me of my time in the mitochondrial disease sequencing space …”
McKernan claims he tried to publish a paper on this in 2021 with Dr. Peter McCullough, but the editor of the journal “stepped in and torpedoed the paper.”12
World’s Largest Side Effect Analysis Has Been Published
In related news, the largest study13 to date on the side effects of the COVID jabs was published in the journal Vaccine in February 12, 2024, and it confirms what I and many other alternative news sources have been saying all along, namely that the mRNA jabs are the most dangerous medical products to ever hit the market.
The study — performed by the Global COVID Vaccine Safety (GCoVS) Project and funded by the U.S. Centers for Disease Control and Prevention, Public Health Ontario and the Canadian Health Research Institute — evaluated the risk of “adverse events of special interest” (AESI) following COVID-19 “vaccination.”
Data from 10 sites in eight countries (Argentina, Australia, Canada, Denmark, Finland, France, New Zealand and Scotland) were included, encompassing more than 99 million jabbed individuals.
Of the thousands of side effects Pfizer listed in its confidential report of post-authorization adverse events submitted to the U.S. Food and Drug Administration,14 the GCoVS focused on 13 AESIs that fall into three primary categories: Neurological, hematologic (blood-related) and cardiovascular conditions.
They calculated the AESI risk for each of the 13 AESIs based on the number of observed versus expected (OE) incidents occurring up to 42 days after injection. The “expected” number of side effects were based on vaccine adverse event data from 2015 to 2019. These rates were then compared to the adverse event rates observed in those who got one or more of the COVID jabs, either Pfizer’s BNT162b2, Moderna’s mRNA-1273, or AstraZeneca’s ChAdOx1.
Largest Study to Date Confirms COVID Jab Dangers
The analysis15 revealed several concerning side effects, including increased risks of myocarditis, pericarditis, blood clots in the brain, and various neurological conditions. Here’s a quick summary of the findings:
•Myocarditis and pericarditis:
◦Pfizer vaccine — OE ratios for myocarditis were 2.78 and 2.86 after the first and second shots, with the risk remaining doubled after the third and fourth shots.
◦Moderna vaccine — OE ratios for myocarditis were 3.48 and 6.10 after the first and second shots. Doses 1 and 4 also showed OE ratios of 1.74 and 2.64 for pericarditis.
◦AstraZeneca vaccine — OE ratio for pericarditis was 6.91 after the third shot.
•Blood clots in the brain (cerebral venous sinus thrombosis, CVST):
◦An OE of 3.23 for CVST was observed after the first AstraZeneca shot.
◦A significant increase in CVST risk was also noted after the second Pfizer dose.
•Neurological conditions:
◦Guillain-Barré syndrome — An OE ratio of 2.49 was observed following the AstraZeneca jab.
◦Transverse myelitis — Risk nearly doubled with the AstraZeneca shot.
◦Acute disseminated encephalomyelitis — OE ratios of 3.78 (Moderna) and 2.23 (AstraZeneca) were noted.
These findings really underscore the potential for serious side effects from the COVID shots, including conditions that may lead to other consequences in the longer term, such as stroke, heart attack, paralysis and death.
Effectiveness and Safety Was Wildly Exaggerated in Trials
Considering those findings, it’s no surprise to find that effectiveness and safety were exaggerated in clinical trials and observational studies. In a guest post on Dr. Robert Malone’s Substack, Raphael Lataster, Ph.D., writes:16
“An unofficial series of four crucially important medical journal articles, two by me, appearing in major academic publisher Wiley’s Journal of Evaluation in Clinical Practice reveals that claims made about COVID-19 vaccines’ effectiveness and safety were exaggerated in the clinical trials and observational studies, which significantly impacts risk-benefit analyses.
Also discussed are the concerning topics of myocarditis, with evidence indicating that this one adverse effect alone means that the risks outweigh the benefits in the young and healthy; and perceived negative effectiveness, which indicates that the vaccines increase the chance of COVID-19 infection/hospitalization/death, to say nothing about other adverse effects.”
Summary of Papers
The four papers in question include:
1.“Sources of Bias in Observational Studies of COVID-19 Vaccine Effectiveness” published in the Journal of Evaluation in Clinical Practice in March 2023, co-authored by BMJ editor Peter Doshi, Ph.D., statistician Kaiser Fung and biostatistician Mark Jones, which concluded that “case-counting window bias” had a significant effect on effectiveness estimates.17
As explained by Lataster, this “concerns the 7 days, 14 days, or even 21 days after the jab where we are meant to overlook jab-related issues, such as COVID infections, for some odd reason as ‘the vaccine has not had sufficient time to stimulate the immune system.’
This may strike you as quite bizarre since all of the ‘fully vaccinated’ must go through the process of being ‘partially vaccinated,’ sometimes even more than once. To make matters worse, the unvaccinated do not get such a ‘grace period,’ meaning that there is also a clear bias at play.
In an example using data from Pfizer’s clinical trial, the authors show that thanks to this bias, a vaccine with effectiveness of 0%, which is confirmed in the hypothetical clinical trial, could be seen in observational studies as having effectiveness of 48%.”
2.“Reply to Fung et. al. on COVID-19 Vaccine Case-Counting Window Biases Overstating Vaccine Effectiveness,” authored by Lataster, which discussed how the counting window bias not only affected effectiveness estimates in observational studies but also safety estimates, suggesting a need for reassessment of vaccine safety.18 The article also addresses “the mysterious rise in non-COVID excess deaths post-pandemic.”19
3.“How the Case Counting Window Affected Vaccine Efficacy Calculations in Randomized Trials of COVID-19 Vaccines,” again co-authored by Doshi and Fung, which detailed how case-counting window issues also overestimated effectiveness in Pfizer and Moderna clinical trials.20
4.A second article by Lataster, in which he highlighted and summarized the evidence showing that clinical trials were affected by adverse effect counting window issues that led to exaggerated safety estimates.21
“Together, these four articles make clear that claims made about COVID-19 vaccines; effectiveness and safety were exaggerated in the clinical trials and observational studies, whilst also finding time to discuss myocarditis and perceived negative effectiveness, meaning that new analyses are very much needed,” Lataster writes.22
Resources for Those Injured by the COVID Jab
Based on data from across the world, it’s beyond clear that the COVID shots are the most dangerous drugs ever deployed. If you already got one or more COVID jabs and are now reconsidering, you’d be wise to avoid all vaccines from here on, as you need to end the assault on your body. Even if you haven’t experienced any obvious side effects, your health may still be impacted long-term, so don’t take any more shots.
If you’re suffering from side effects, your first order of business is to eliminate the spike protein — and/or any aberrant off-target protein — that your body is producing. Two remedies shown to bind to and facilitate the removal of SARS-CoV-2 spike protein are hydroxychloroquine and ivermectin. I don’t know if these drugs will work on off-target proteins and nanolipid accumulation as well, but it probably wouldn’t hurt to try.
The Front Line COVID-19 Critical Care Alliance (FLCCC) has developed a post-vaccine treatment protocol called I-RECOVER. Since the protocol is continuously updated as more data become available, your best bet is to download the latest version straight from the FLCCC website at covid19criticalcare.com.23
For additional suggestions, check out the World Council for Health’s spike protein detox guide,24 which focuses on natural substances like herbs, supplements and teas. Sauna therapy can also help eliminate toxic and misfolded proteins by stimulating autophagy.
This documentary cuts to the core of the case against so-called Covid vaccines: Instead of protecting against Covid, the injections are injuring and killing so many people that the process has become nothing less than genocide – which is not so surprising when we learn that the masterminds behind these shots are fierce advocates of population reduction. The documentary revolves around a group of embalmers and coroners who independently discovered that, starting precisely at the time the alleged vaccines were introduced, the number of “sudden” deaths began skyrocketing to levels never seen before – and they discovered the cause. You will see them remove long, worm-like fibers from the main arteries and veins of “sudden-death” victims. These grotesque killers are so large, they completely block the flow of blood to vital organs. All of these victims had been vaccinated. 2022 Nov 27 – Source: Stu Peters Productions.
Within hours following the release of this documentary, the so-called fact checkers began flooding the Internet with claims that the program is an absurd conspiracy theory loaded with false claims. Let us hope that someone, soon, will fact-check the fact checkers and, when they do, the first thing they will notice is that the main thrust of the story is centered around a group of embalmers who independently reported finding strange, fibrous blood clots in the arteries and veins of cadavers who had taken the Covid injections – but not in those who had rejected it. Then they will notice that the fact checkers have nothing to say about any of that. Instead, they focus on the claim that some of the video clips showing people suddenly dropping to the floor and convulsing may have been taken before Covid began or that the people may not have died after their collapse. These claims, of course, also need to be checked. If they are true, it would be unfortunate that the video editor failed to be more selective in the choice of images, but it would in no way diminish the importance of the main theme of the film, which is that a never-before-seen type of blood clot started appearing in cadavers a few months following the introduction of the inoculation program and that, during this same period, the death rate from all causes began to skyrocket. Since this is the main message from the documentary and the fact checkers have nothing to say about it, must not be overlooked.
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