Many COVID-19 vaccines, like those of Pfizer and Moderna, are mRNA vaccines. Despite the fact that mRNA vaccine technology was never used on humans before* the power elite promoted its use on a global scale, including children. There are some things about these mRNA vaccines that they don't tell you...

In theory...

mRNA contained in lipid nanoparticles is injected into the muscle in the shoulder, enters the muscle cells and then instructs those cells to produce a spike protein similar to that of the SARS-CoV-2 virus. That spike protein is used by the virus to enter and infect the host cell. Then the foreign mRNA and spike proteins are removed from the body within days.

The spike protein binds to the ACE2 recepter on the surface of the cells.* ACE2 is present in many cell types and tissues including the lungs, heart, blood vessels, kidneys, liver and gastrointestinal tract.* Because it is a foreign protein the immune system reacts and precipitates antibodies which are proteins made by your immune system to protect you.* This way the immune system learns how to reduce your reaction to SARS-CoV-2 if you get it. This is the theoretical story as it was sold to the public. According to the power elite and their media the mRNA generated spike proteins are "harmless"* and "perfectly safe"*. But is this true?

Spike proteins downregulate protective ACE2...

The Pfizer/BioNTech vaccine (BNT162b2) is composed of an mRNA that produces a membrane-anchored full-length spike protein. The mouse studies suggest that an untruncated form of the S1 protein like this may cause a microvasculopathy in tissues that express much ACE2 receptor.*

It was shown that the spike protein readily crossed the blood–brain barrier in male mice, was taken up by brain regions and entered the parenchymal brain space and was also taken up by the lung, spleen, kidney and liver when injected into the bloodstream of mice.

ACE2 is protective in the cardiovascular system, and SARS-CoV-1 S protein promotes lung injury by decreasing the level of ACE2 in the infected lungs. ... S protein alone can damage vascular endothelial cells (ECs) by downregulating ACE2 and consequently inhibiting mitochondrial function.

If one removes the replicating capabilities of the virus, it still has a major damaging effect on the vascular cells, simply by virtue of its ability to bind to this ACE2 receptor.* Researchers also reported that papers showed that the spike protein by itself (without being part of the corona virus) can damage endothelial cells and disrupt the blood-brain barrier.

Autoimmune disease...

Because of the damaging effects of Spike proteins binding to ACE2 receptors of healthy cells it is important that the lipid nanoparticles with mRNA or the resulting spike proteins stay in the shoulder at the site of injection as much as possible and don't travel through the body. Because if they travel freely through the body then the immune system's cytotoxic T cells will kill the foreign spike proteins attached to the ACE2 on their surfaces together with the healthy cells of those organs. Autoimmunity is when the immune system attacks healthy cells of its own healthy organs. And this is what happened. These vaccines have been linked to autoimmune disease. Autoimmunity and the opposing condition, metabolic syndrome, are well known adverse events caused by vaccines.

The importance of aspiration

Because of the damaging effects of a high concentration of the vaccine it may never be injected into the bloodstream directly. But also the idea of intramuscular injection is that muscles have good vascularity and the injected vaccine can quickly reach the systemic circulation which is the part of the vascular system that carries blood from the heart to organs and tissues of the body. It then also reaches the lymphatic system, an important part of the immune system, with the spleen which is part of the circulatory blood system. So, an undefined percentage of these damaging mRNA nanoparticles will always enter the bloodstream, even with intramuscular injection. In June 2021 the "fact-checkers" of the power elite told the world that the spike proteins stay in the shoulder muscle...

screenshot

In May 2021 the spike proteins produced by the mRNA vaccines were found in the blood of vaccinated people...

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) proteins were measured in longitudinal plasma samples collected from 13 participants who received two doses of mRNA-1273 vaccine. Eleven of 13 participants showed detectable levels of SARS-CoV-2 protein as early as day 1 after first vaccine injection. ... critical data demonstrating the direct production of spike protein via translation from the mRNA-1273 vaccine in these studies are missing, precluding a full understanding of the vaccine mechanism.

In August 2021 a research of a test on mice concluded...

This study provided in vivo evidence that inadvertent intravenous injection of COVID-19 mRNA vaccines may induce myopericarditis. Brief withdrawal of syringe plunger to exclude blood aspiration may be one possible way to reduce such risk.

In October 2021 the Korea Herald reported that wrongly administering COVID-19 vaccines into blood vessels instead of the muscles could be behind the serious side effects.* In April 2022 Germany changed protocols to include aspiration for mRNA vaccination.* So because it's important that the lipid nanoparticles with mRNA stay at the site of injection the nurse can check whether the needle punctured a blood vessel by doing aspiration, drawing back of the syringe to check for blood. If blood is present the nurse can change the injection location. Remarkably, at least until the beginning of August 2022 the CDC advised to not do aspiration...

screenshot

mRNA vaccination stimulates robust GCs containing vaccine mRNA and spike antigen up to 8 weeks postvaccination in some cases.

See also Chris Martenson's video about this paper*. In June 2022 researchers headlined Vaccine mRNA Can Be Detected in Blood at 15 Days Post-Vaccination.

Circulating exosomes expressing spike proteins...

The identification of several molecules involved in processes such as immune response, and inflammation, the activation of coagulation and complement pathways could link circulating exosomes to COVID-19–associated tissue damage and multiple organ dysfunctions.

Results demonstrated induction of circulating exosomes expressing spike protein on day 14 after vaccination followed by Abs 14 d after the second dose. Exosomes with spike protein, Abs to SARS-CoV-2 spike, and T cells secreting IFN-γ and TNF-α increased following the booster dose. Transmission electron microscopy of exosomes also demonstrated spike protein Ags on their surface. Exosomes with spike protein and Abs decreased in parallel after four months. These results demonstrate an important role of circulating exosomes with spike protein for effective immunization following mRNA-based vaccination.

After vaccination the spike protein was found in exosomes which travel through the body for about four months. Exosomes are implicated in cell–cell communication and the transmission of disease states.

The spike protein impairs DNA repair mechanisms

The following research shows that the spike protein impedes the DNA repair mechanism...

SARS–CoV–2 spike protein significantly inhibits DNA damage repair, which is required for effective V(D)J recombination in adaptive immunity. Mechanistically, we found that the spike protein localizes in the nucleus and inhibits DNA damage repair by impeding key DNA repair protein BRCA1 and 53BP1 recruitment to the damage site. Our findings reveal a potential molecular mechanism by which the spike protein might impede adaptive immunity and underscore the potential side effects of full-length spike-based vaccines.

The spike protein is neurotoxic, and it impairs DNA repair mechanisms.

The DNA repair mechanism identifies and corrects damage to the DNA molecules that encode the genome. It prevents harmful mutations which could lead to for example cancer or other diseases. That the spike protein created by the vaccines impedes this extremely important mechanism doesn't sound like something to ignore or to take lightly when considering vaccination. Of course the power elite won't tell you about it because it would undermine their lucrative global vaccination plan. See vacciNATION.

screenshot

A higher-than-usual number of cases of a type of heart inflammation has been reported following Covid-19 vaccination, especially among young men following their second dose of an mRNA vaccine.*

Since April 2021, increased cases of myocarditis and pericarditis have been reported in the United States after mRNA COVID-19 vaccination.*

Events of Myocarditis and Pericarditis have been reported. ... Post-authorization reports have been reported more frequently in adolescent and young adult male patients following the second dose of vaccine; however, reports have been received for adult males and females of broader age range and following the first vaccination also.*

Findings raise concerns regarding vaccine-induced undetected severe cardiovascular side-effects and underscore the already established causal relationship between vaccines and myocarditis.

If organizations like CDC, EMA and the mainstream media are reporting it, it is probably more serious than they make it seem. Myocarditis weakens the heart so that the rest of the body doesn't get enough blood. Clots can form in the heart, leading to a stroke or heart attack.

screenshot

These statistics clearly show what's going on. According to VAERS there were in total 972 reported cases of myocarditis and pericarditis in the US after any vaccination given between 1990 and the present while there were in total 21,479 reported cases after COVID-19 vaccination alone.** And keep in mind that these events are heavily underreported, see VacciNATION.

Vaccine-encoded spike protein seems to reach the heart, where it might trigger an inflammatory response, resulting in the development of myocarditis or DCMi.

There's strong evidence of an increased risk of myocarditis and of pericarditis in the week following vaccination against Covid-19 with mRNA vaccines.

While myopericarditis is strongly linked to mRNA vaccination researchers published a paper of a large study in April 2022 in which they did not observe an increased incidence of neither pericarditis nor myocarditis in adult patients recovering from COVID-19 infection. So whether COVID-19 causes heart problems, as stated by the power elite and their media, is doubtful, but there are plenty indications that the vaccines do.

A blood clot or thrombus is an accumulation of blood that forms into a clot that has the potential to slow blood flow inside a blood vessel, sometimes even blocking blood flow completely. It is known that blood clotting is caused by the virus spike protein. Although the power elite and their media downplay the occurrence of blood clots after mRNA vaccinations which induce these spike proteins, there are several independent pathologists around the world who performed autopsies on deceased vaccinees that reveal extreme blood clotting. For example Ryan N. Cole found many clots in deceased vaccinated people. Resia Pretorius stated that all COVID-19 vaccines might also sometimes trigger subtler clotting issues. ...vaccination can lead to microclots.

Vaccination with ChAdOx1 nCov-19 can result in the rare development of immune thrombotic thrombocytopenia.

Although rare, VITT is a new phenomenon with devastating effects for otherwise healthy young adults and requires a thorough risk–benefit analysis. The findings of our study indicate that VITT may be more frequent than has been found in previous studies in which the safety of the ChAdOx1 nCoV-19 vaccine has been investigated.

In March 2021, concerns developed regarding an increased risk of thrombosis associated with thrombocytopenia among persons who had received ChAdOx1 nCoV-19. By the end of the month, groups from Norway, Germany, Austria, and the United Kingdom reported on persons admitted to the hospital 5 to 24 days after vaccination with ChAdOx1 nCoV-19. These patients had thrombosis at unusual sites... Most of these patients were previously fit, healthy young persons.

The related adverse event is called vaccine-induced immune thrombotic thrombocytopenia, or VITT. Despite these findings the "fact-checkers" of the power elite stated in August 2021 that there is no evidence that mRNA vaccines are linked to blood clots* while later in December 2021 scientists stated that research is not definitive* and several studies already showed the link. In April 2021 health alerts were issued even by for example CDC* and EMA* in which they downplay the occurrence stating that it is extremely "rare" and there's nothing to worry about. The power elite and their media say that patients should be reassured that the benefits of vaccination against COVID-19 far outweigh any potential risk* while healthy people have nothing to fear from a flu like Covid. See COVID-1984.

The UK Health Security Agency (UKHSA), Public Health Scotland, Public Health Wales and the Public Health Agency are continuing to investigate a rise in cases of sudden onset hepatitis (liver inflammation) in children aged 10 and under since January 2022, where the usual viruses that cause infectious hepatitis (hepatitis A to E) have not been detected.**

Since late 2021 also children are being injected with these experimental vaccines. The results are now starting to show in the form of hepatitis, liver inflammation. It was already known from animal experiments that lipids containing mRNA were found circulating the body after intramuscular injection, and the site where most was found was in the liver. This means that cells in the liver and other body parts started producing damaging spike proteins. A Pfizer study, released in November 2020 after the FOIA, stated...

The concentrations of [3 H]-08-A01-C01 were greatest in the injection site at all time points, with levels peaking in the plasma by 1-4 hours post-dose and distribution mainly into liver, adrenal glands, spleen and ovaries over 48 hours. Total recovery of radioactivity outside of the injection site was greatest in the liver...

This is the first reported episode of autoimmune hepatitis developing post-COVID-19 vaccination, raising concern regarding the possibility of vaccine-induced autoimmunity. As causality cannot be proven, it is possible that this association is just coincidental. However, severe cases of SARS-CoV-2 infection are characterized by an autoinflammatory dysregulation that contributes to tissue damage. As the viral spike protein appears to be responsible for this, it is plausible that spike-directed antibodies induced by vaccination may also trigger autoimmune conditions in predisposed individuals.

Our results indicate a fast up-take of BNT162b2 into human liver cell line Huh7, leading to changes in LINE-1 expression and distribution.

COVID19 vaccination can elicit a distinct T cell-dominant immune-mediated hepatitis with a unique pathomechanism associated with vaccination induced antigen-specific tissue-resident immunity requiring systemic immunosuppression.

SARS-CoV-2 vaccination can be associated with liver injury [and] this large international case series provides evidence for the hepatotoxicity potential of SARS-CoV-2 vaccines (Pfizer-BioNTech, Moderna and Oxford-AstraZeneca).

So the link between mRNA vaccinations and possible problems with the liver and other organs is real. The power elite also expose children to these experimental vaccines eventhough children are as good as not affected by COVID, although they are risked for side effects of these vaccines. See COVID-1984.

screenshot

According to the power elite who make profit from the sale of vaccines and who are in control of the mass information spread via their mainstream media there's of course absolutely nothing wrong with these vaccines and they are thus also not linked to immunodeficiency. However...

For any given viral copy number, the odds of anti-N seropositivity were 13.67 times higher for the placebo arm than the vaccine arm (95% CI 5.17, 36.16). For example, a vaccine recipient with 2.0 log10 viral copies/ml on illness visit has an estimated probability of PDV anti-N seropositivity of 0.15, while for a placebo recipient with the same illness visit viral copy number, the estimated probability is 0.71 (Figure 2B).

An infection with the virus will expose the complete virus to the immune system, but the vaccines only introduce the spike protein of the virus. So in essence the vaccines create antibodies against the spike protein, not neccessarily against the complete virus including for example its nucleus or nucleocapsid containing the RNA. Infection with the virus also creates anti-nucleocapsid antibodies. The spike protein mutates rapidly and the nucleus mutates slowly which might explain why so many vaccinees get re-infected with virus mutations while the unvaccinated are better protected. This understates the superiority of natural immunity as opposed to vaccine immunity.

With the repeating booster shots it seems that people who start taking these vaccinations will need more and more vaccinations simply because their natural immune system becomes more and more dysfunctional. If your natural immune system is not trained well, by for example repeatedly bypassing it with vaccination, it will become weak.* It is called acquired immunodeficiency or Vaccine-Acquired Immune Deficiency Syndrome, or simply VAIDS.

Most of these vaccines have been approved without extensive studies on their side-effects and efficacy. Recently, new-onset autoimmune phenomena after COVID-19 vaccination have been reported increasingly (e.g. immune thrombotic thrombocytopenia, autoimmune liver diseases, Guillain-Barré syndrome, IgA nephropathy, rheumatoid arthritis and systemic lupus erythematosus).

If we have a strategy in which we give boosters every four months, we will end up potentially having problems with immune response.*

This immune phenomenon known as 'tolerance' where if you already have high antibody levels and you get another booster that your immune system can start to say, well, 'what am I needed for?' and can kind of start to shut down.*

The decrease in immunity can be caused by several factors such as N1-methylpseudouridine, the spike protein, lipid nanoparticles, antibody-dependent enhancement, and the original antigenic stimulus.

In this image we see that the BNT162b2 mRNA vaccine even causes "negative" immunity at 18 weeks after the first dose. This means that, eventhough it may boost immunity temporarily, it eventually destroys natural immunity and makes the vaccinated person weaker...

People infected with the omicron variant show poor immunity boosting against future covid-19 infection... This may explain why breakthrough and repeat infections have been a common feature of the omicron wave of the pandemic, even among people who have been triple vaccinated, said the research team.

It might have to do with the fact that the Omicron variant of SARS-CoV-2 carries multiple spike mutations with high transmissibility and partial neutralizing antibody escape. What can be safely stated is that repeated vaccinations will make the health of vaccinees more and more dependent on the power elite and their more and more profitable pharmaceutical industry.

On their countless pro-vaccination propaganda websites about these mRNA vaccines the power elite boldly state that mRNA vaccines can't change your DNA* and that COVID-19 vaccines do not change or interact with your DNA in any way.* But for example the following study suggests that these new mRNA vaccines can cause permanent changes to the genome which contains the DNA of the receiver by means of reverse-transcription...

We show here that SARS-CoV-2 RNA can be reverse-transcribed and integrated into the genome of the infected cell and be expressed as chimeric transcripts fusing viral with cellular sequences. Importantly, such chimeric transcripts are detected in patient-derived tissues.

This research was done because scientists discovered that PCR tests detected segments of viral RNA even when the virus was presumably cleared from the patients’ bodies and they were not re-exposed to the virus.* On 13 May 2021 one of its authors, Rudolf Jaenisch, stated:

In the new [PNAS] paper, we now have unambiguous evidence that these viral sequences are integrated into the genome. The most common mechanism [for this] is what’s called LINE1-mediated retroposition, coming from the footprints of the viral sequence in the genome. It’s irrefutable. They can integrate.*

Retroviruses ... carry genes that reverse transcribe RNA back into complementary DNA. ... More than a third of the human genome is devoted to mysterious mobile DNA elements called SINEs and LINEs (...). LINEs provide reverse transcriptase capabilities to convert RNA into DNA, and SINEs provide support for integrating the DNA into the genome.

DNA encodes the genetic instructions used in the development and functioning of all known living organisms and viruses. It's unique for every individual and determines what physical characteristics someone has as well as what diseases someone may develop. Changing DNA is part of genetic engineering, which of course involves important ethical questions, certainly when it concerns human beings.

screenshot

The so-called "fact-checkers" of the power elite tried to downplay this information by stating that this study co-authored by MIT biologists did not conclude that COVID-19 vaccines would change the recipient’s DNA. But in the same article it is mentioned that this research validates that this is at least plausible, and most likely probable.

In December 2017 Tal Zaks, the Chief Medical Officer of Moderna Therapeutics, a company that produced mRNA vaccines for COVID-19, said that mRNA injections can be used for the purpose of genetic engineering. He calls it the hacking of the software of life.* So the possibility of mRNA changing your DNA is simply a fact and whether it happens after these mRNA injections remains to be seen in the long run. At the World Health Summit in 2021 Stefan Oelrich, head of Bayer, a major pharmaceutical company, said the following...

Ultimately, the mRNA vaccines are an example for that cell and gene therapy. I always like to say that if we had surveyed two years ago in the public 'Would you be willing to take gene cell therapy injected into your body?' we would have probably had a 95% refusal rate. I think this pandemic has also opened many people's eyes to innovation in the way that was maybe not possible before.

mRNA vaccination is a step in the process towards genetic engineering of humans. In February 2022 researchers published a paper of an in vitro test saying that BNT162b2 mRNA is reverse transcribed intracellularly into DNA in as fast as 6 h upon BNT162b2 exposure. What's for sure is that what is injected into the body cannot be taken out and that the authorities lied when they said that these vaccines could and would not affect your DNA.

This typical pro-vaccination propaganda video opens with a quote about a polio vaccine, but obviously one can't simply compare polio with COVID-19, the polio vaccine was not an mRNA vaccine to begin with. They make it seem as if these vaccines are perfectly safe, but the fact that they were approved under a so-called Emergency Use Authorization by the FDA shows that these vaccines didn't undergo all the required safety tests. See VacciNATION. If a new vaccine is produced within 11 months instead of the regular 10 to 15 years then of course the long-term side effects are still unknown and nobody can possibly know if these vaccines are safe. Eventhough this video suggests that a new mRNA vaccine can be created within three weeks, we haven't seen any new mRNA vaccines for all the known COVID-19 variants for which the original vaccine is shown to be as good as useless. This may well have to do with the fact that the power elite first want to sell the old vaccines to maximize profit before selling you a new and more effective one. It's not about people, but about profit. Quickly produced mRNA vaccines are more profitable because the expensive safety trials are not done. Now everybody knows that none of these vaccines prevented people from getting (re)infected and spreading the virus.