Unintended Consequences of mRNA Vaccines Against COVID-19
MIT scientist Stephanie Seneff’s paper, “Worse Than the Disease: Reviewing Some Possible Unintended Consequences of mRNA Vaccines Against COVID-19,” published in the International Journal of Vaccine Theory, Practice and Research in collaboration with Dr. Greg Nigh, is still one of the best, most comprehensive descriptions of the many possible unintended consequences of the mRNA gene transfer technologies incorrectly referred to as “COVID vaccines.”
December 9, 2021, their paper was reprinted in the Townsend Letter, the Examiner of Alternative Medicine. Seneff, Ph.D., a senior research scientist at MIT who has been conducting research at MIT for over five decades, has spent a large portion of her career investigating the hazards and mechanisms of action of glyphosate.
Her attention was diverted to the science of mRNA gene transfer technologies in early 2020, when Operation Warp Speed was announced. As noted in her paper, many factors that lacked precedent, yet were being implemented at breakneck speed, included:
- The first-ever use of PEG (polyethelene glycol) in an injection
- The first-ever use of mRNA gene transfer technology against an infectious agent
- The first-ever “vaccine” to make no clear claims about reducing infection, transmissibility or death
- The first-ever coronavirus vaccine ever tested on humans (and previous coronavirus vaccines all failed due to antibody-dependent enhancement, a condition in which the antibodies actually facilitate infection rather than defend against it)
- The first-ever use of genetically modified polynucleotides in the general population
An Insanely Reckless Process
In a May 2021 interview with me, Seneff said:
“To have developed this incredibly new technology so quickly, and to skip so many steps in the process of evaluating [its safety], it’s an insanely reckless thing that they’ve done. My instinct was that this is bad, and I needed to know [the truth].
So, I really dug into the research literature by the people who’ve developed these vaccines, and then more extensive research literature around those topics. And I don’t see how these vaccines can possibly be doing anything good …”
At the time, just five months into the mass inoculation campaign, Seneff suspected the COVID shots would end up killing far more people than the infection itself. Today, a full year into it, the statistics are grim beyond belief, proving her educated prediction to have been an astute one.
mRNA Jabs Are Shockingly Hazardous
As of December 3, 2021, the U.S. Vaccine Adverse Event Reporting System (VAERS) has logged an astounding 927,738 COVID jab related adverse events, including 19,886 deaths. VAERS can receive reports from vaccine manufacturers and other international sources, and if we exclude those, the death toll reported in U.S. territories exclusively stands at 9,136.
Of the total death reports, Pfizer — the only company that the U.S. Food and Drug Administration has granted full licensing for an as-yet unavailable COVID shot — accounts for the vast majority: 13,268, compared to 4,894 for Moderna, 1,651 for Janssen and 73 for an undisclosed brand.
Pfizer also accounts for the vast majority of hospitalizations post-injection, and while those over the age of 66 make up the bulk of deaths, the 25-to-50 age group accounts for most of the hospitalizations. Key side effects that are now being reported in massive numbers include:
- Miscarriages
- Heart problems such as heart attacks and myopericarditis
- Thrombocytopenia (low platelet count)
- Shingles
- Bell’s palsy
- A variety of permanent disabilities, many of which involve neurological dysfunction
All of these consequences were predicted by Seneff and Nigh in their paper, which makes the events all the more tragic. Importantly, VAERS is notoriously underreported, so the real-world impact of these shots is far greater than what those data suggest.
The Cure Is Indeed Worse Than the Disease
Calculations performed by Steve Kirsch, executive director of the COVID-19 Early Treatment Fund, and his team of statisticians suggest VAERS COVID-related reports are underreported by a factor of 41. This is a conservative estimate, supported by calculations using a variety of sources besides VAERS itself.
That means that in the U.S. alone (using the data for U.S. territories only), the actual death toll may be closer to 374,576 (including international deaths reported to VAERS would put the death toll at 815,326), and those are deaths that occurred within days or weeks post-injection.
As Seneff and Nigh explain in their paper, there’s overwhelming reason to suspect that these gene transfer injections will have devastating impacts in the long term, resulting in excess deaths over the next decade.
What’s more, it’s clear that the death toll from the COVID-19 infection itself in the U.S. has been vastly exaggerated, as it’s based on positive PCR tests and even mere suspicion of COVID in the absence of testing. Many died from other causes and just happened to have a positive COVID test at the time of death.
Kirsch estimates the real death tally from COVID-19 to be about 50 percent of the reported number (which is likely conservative). This means about 380,000 Americans died from COVID-19 (rather than with COVID), whereas the COVID shots may have killed more than 374,570 in the first 11 months alone.
“Seneff suspects that in the next 10 to 15 years, we’ll see a dramatic spike in prion diseases, autoimmune diseases, neurodegenerative diseases at younger ages, and blood disorders such as blood clots, hemorrhaging, stroke and heart failure.”
As predicted in the title of Seneff’s paper, it seems the cure may indeed end up being worse than the disease. This is particularly true for children and young adults, who have either died or been permanently disabled by the shots by the thousands, while having an extraordinarily low risk of dying from or being seriously harmed by the infection itself.
The Spike Protein Is the Most Dangerous Part of SARS-CoV-2
The reason we’re seeing all these problems from the COVID shots is because they program your cells to continuously produce SARS-CoV-2 spike protein, which we now know is the most dangerous part of the virus. Many experts noted this from the start, wondering what the vaccine developers could possibly be thinking, selecting this as the antigen for their shots.
While the mRNA injections can cause harm in many different ways, one basic problem is that they can overstimulate your immune system to the point of failure. In summary, as your cells start producing the viral spike proteins, your immune cells rally to mop up the proteins and dump them into your lymphatic system. (This is why many report swollen lymph nodes under the arms.)
The antibody response is part of your humoral immunity. You also have cellular immunity, which is part of your innate immune system. Your innate immune system is very powerful. If you’re healthy, it can clear viruses without ever producing a single antibody. Antibodies are actually a second-tier effect when your innate immune system fails.
The problem is that your innate immune system will not be activated and likely will fail to protect you if you get a COVID-19 shot, because it’s bypassing all of the areas where your innate immune system would be brought to bear.
Normally you breathe the virus in and stimulate the production secretory IgA antibodies that protect your respiratory system. When you bypass that route of exposure with a jab in the arm, no secretory IgA antibodies are produced, leaving you susceptible to the infection.
As explained by Ronald Kostoff in an excellent December 8, 2021, Trial Site News article, “COVID-19 ‘Vaccines’: The Wrong Bomb Over the Wrong Target at the Wrong Time”:
“An effective vaccine would focus on cellular immunity in the respiratory and intestinal tract, in which secretory IgA is produced by your lymphocytes that are located directly underneath the mucous membranes that line the respiratory and intestinal tract.
The antibodies produced by these lymphocytes are ejected through and to the surface of the linings. These antibodies are thus on site to meet air-borne viruses and they may be able to prevent viral binding and infection of the cells.
Unfortunately, the main inoculants used presently for COVID-19 focus on antibodies (IgG and circulating IgA) that occur in the bloodstream. These antibodies protect the internal organs of the body from infectious agents that try to spread via the bloodstream.”
When you are injected with the COVID jab, your body will only induce IgG and circulating IgA — not secretory IgA, and these types of antibodies do not effectively protect your mucous membranes from SARS-CoV-2 infection. So, as noted by Kostoff, the breakthrough infections we’re now seeing “confirm the fundamental design flaws” of this gene transfer technology.
“A natural infection with SARS-CoV-2 (coronavirus) will in most individuals remain localized to the respiratory tract,” Kostoff writes. “The vaccines used presently cause cells deep inside our body to express the viral spike protein, which they were never meant to do by nature.
Any cell which expresses this foreign antigen on its surface will come under attack by the immune system, which will involve both IgG antibodies and cytotoxic T-lymphocytes. This may occur in any organ, but the damage will be most severe in vital organs.
We are seeing now that the heart is affected in many young people, leading to myocarditis or even sudden cardiac arrest and death. In other words, we are dropping the wrong bomb on the wrong target at the wrong time!”
In the end, your body will essentially believe that your innate immune system has failed, which means it must bring in the backup cavalry. In essence, your body is now overreacting to something that isn’t true. You’re not actually infected with a virus and your innate immune system has not failed, but your body is forced to respond as if both are true.
Effects Likely to Persist Long Term
What’s more, the synthetic RNA in the mRNA vaccines contains a nucleotide called methyl-pseudouridine, which your body cannot break down, and the RNA is programmed to trigger maximum protein production. So, we’re looking at completely untested manipulation of RNA.
It is very important to recognize that this is a genetically engineered mRNA for the spike protein. It is not identical to the spike protein mRNA that SARS-Cov-2 produces. It’s been significantly altered to avoid being metabolized by your body.
The spike protein your body produces in response to the COVID-19 vaccine mRNA locks into your ACE2 receptor. This is because the genetically engineered new spike protein has additional prolines inserted that prevent the receptors from properly closing, which then cause you to downregulate ACE2. That’s partially how you end up with problems such as pulmonary hypertension, ventricular heart failure and stroke.
As noted in a 2020 paper, there’s a “pivotal link” between ACE2 deficiency and SARS-CoV-2 infection. People with ACE2 deficiency tend to be more prone to severe COVID-19. The spike protein suppresses ACE2, making the deficiency even worse. According to Seneff, the gene transfer injections essentially do the same thing, and we still don’t know how long the effects last.
Manufacturers initially guessed the synthetic RNA might survive in the human body for about six months. A more recent investigation found the spike protein persisted in recovered COVID patients for 15 months.
This raises the suspicion that the synthetic and more persistent mRNA in the COVID shots may trigger spike protein production for at least as long, and probably longer. What’s more, the number of spike proteins produced by the shots is far greater than what you experience in natural infection.
As explained by Dr. Peter McCullough, this means that after your first shot, your body will produce spike protein for at least 15 months. But, when you get shot No. 2 a few weeks later, that shot will cause spike protein production to go on for 15 months or longer. With shot No. 3 six months after that, you produce spike protein for yet another 15 months.
With regular boosters, you may never rid your body of the spike protein. All the while, it’s wreaking havoc with your biology. McCullough likens it to “a permanent install of an inflammatory protein in the human body,” and inflammation is at the heart of most if not all chronic diseases. There’s simply no possible way for these gene transfer shots to improve public health. They’re going to decimate it.
Long-Term Neurological Damage Is To Be Expected
In her paper, Seneff describes several key characteristics of the SARS-CoV-2 spike protein that suggests it acts as a prion. This could help explain why we’re seeing so many neurological side effects from the shots. According to Seneff, the spike protein produced by the COVID shot, due to the modifications made, may actually make it more of a prion than the spike protein in the actual virus, and a more effective one.
For a detailed technical description of this you can read through Seneff’s paper, but the take-home message is that COVID-19 shots 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, radically increasing your risk of developing neurodegenerative diseases.
Lung, Heart and Brain Diseases Are Predictable Consequences
Seneff also goes into great detail describing how the spike protein acts as a metabolic poison. While I recommend reading Seneff’s paper in its entirety, I’ve extracted some key sections below, starting with how the spike protein can trigger pathological damage leading to lung damage and heart and brain diseases:
The picture is now emerging that SARS-CoV-2 has serious effects on the vasculature in multiple organs, including the brain vasculature … In a series of papers, Yuichiro Suzuki in collaboration with other authors presented a strong argument that the spike protein by itself can cause a signaling response in the vasculature with potentially widespread consequences.
These authors observed that, in severe cases of COVID-19, SARS-CoV-2 causes significant morphological changes to the pulmonary vasculature … Furthermore, they showed that exposure of cultured human pulmonary artery smooth muscle cells to the SARS-CoV-2 spike protein S1 subunit was sufficient to promote cell signaling without the rest of the virus components.
Follow-on papers showed that the spike protein S1 subunit suppresses ACE2, causing a condition resembling pulmonary arterial hypertension (PAH), a severe lung disease with very high mortality … The ‘in vivo studies’ they referred to … had shown that SARS coronavirus-induced lung injury was primarily due to inhibition of ACE2 by the SARS-CoV spike protein, causing a large increase in angiotensin-II.
Suzuki et al. (2021) went on to demonstrate experimentally that the S1 component of the SARS-CoV-2 virus, at a low concentration … activated the MEK/ERK/MAPK signaling pathway to promote cell growth. They speculated that these effects would not be restricted to the lung vasculature.
The signaling cascade triggered in the heart vasculature would cause coronary artery disease, and activation in the brain could lead to stroke. Systemic hypertension would also be predicted. They hypothesized that this ability of the spike protein to promote pulmonary arterial hypertension could predispose patients who recover from SARS-CoV-2 to later develop right ventricular heart failure.
Furthermore, they suggested that a similar effect could happen in response to the mRNA vaccines, and they warned of potential long-term consequences to both children and adults who received COVID-19 vaccines based on the spike protein.
An interesting study by Lei et. al. (2021) found that pseudovirus — spheres decorated with the SARS-CoV-2 S1 protein but lacking any viral DNA in their core — caused inflammation and damage in both the arteries and lungs of mice exposed intratracheally.
They then exposed healthy human endothelial cells to the same pseudovirus particles. Binding of these particles to endothelial ACE2 receptors led to mitochondrial damage and fragmentation in those endothelial cells, leading to the characteristic pathological changes in the associated tissue.
This study makes it clear that spike protein alone, unassociated with the rest of the viral genome, is sufficient to cause the endothelial damage associated with COVID-19. The implications for vaccines intended to cause cells to manufacture the spike protein are clear and are an obvious cause for concern.”
The COVID Shots Activate Latent Viruses
As mentioned earlier, shingles infection is turning out to be a rather common side effect of the COVID shot, and like the neurological, vascular and cardiac damage we’re seeing, activation of latent viral infections was also predicted.
One reason why latent viral infections are cropping up in response to the shots is because the shots disable your type I interferon pathway. A second reason is because your immune system is overburdened trying to deal with the inflammatory spike proteins flowing through your body. Something’s got to give, so latent viruses are allowed to break through.
That’s not the end of your potential troubles, however, as these coinfections may worsen or accelerate other conditions, such as Bell’s Palsy, myalgic encephalomyelitis and chronic fatigue syndrome.
Herpes viruses, for example, have been implicated as a trigger of both AIDS and chronic fatigue syndrome. Some research suggests these diseases don’t appear until viruses from different families partner up and the type 1 interferon pathway is disabled.
With all of that in mind, it seems inevitable that, long term, the COVID mass injection campaign will result in an avalanche of a wide range of debilitating chronic illnesses.
See more here: theepochtimes.com
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Tom
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Big pharma’s creed: Unintended consequences lead to INTENDED profits! We are seeing it up close and personal.
Reply
JaKo
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In conclusion:
All who profited from the covidian scam shall be “immunized” and “boosted” until their natural demise…
Cheers, JaKo
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Melinda
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Immunize them with LEAD. Forget the boosters.
Reply
Richard Noakes
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If you think that the consequences of the vaccines were “unintended” then you are a fool:
Official Biochemical and Statistical Evidence 100% confirms Moderna created Covid-19
By The Exposé on March 3, 2022
Evidence has emerged which proves beyond a reasonable doubt that the pharmaceutical giant Moderna, the company that has made billions through the sale of an experimental Covid-19 injection, actually created the Covid-19 virus.
Covid-19 means: 19 nucleotide sequence and not 2019 at all.
On February 23 the Daily Mail ran an article showing that Moderna has patented the 19 base letter (nucleotide) sequence which codes for the Furin Cleavage site in Covid-19.
By a concerned reader
They cited a Paper by Scientists in India, Switzerland, Italy and the US (cautiously entitled: MSH3 Homology and Potential Recombination Link to SARS-CoV-2 Furin Cleavage Site) in which they calculated that the chances of a 19 nucleotide sequence patented by Moderna randomly appearing in Covid-19 in circumstances where it does not appear anywhere else in nature are 1 in 3 trillion.
Furthermore they did not merely apply for a patent on 2016 February 4 with US9587003B2: as reported in the Daily Mail. They actually applied on 2013 December 16 for 4 patents with US9149506B2, US9216205B2, US9255129B2, US9301993B2:as well.
So Moderna had developed the 19 nucleotide gene sequence containing the Furin Cleavage Site which gives Covid19 its infectivity to humans by patented gain of function research as early as 2013, 6 years before the Wuhan outbreak took place. Not 3 as reported in the Mail and virally elsewhere..
The Expose
Scientists find virus contains tiny chunk of DNA that matches sequence patented by Moderna THREE YEARS before pandemic began –Genetic match discovered in Covid’s unique furin cleavage site on spike protein –Matched genetic sequence patented by Moderna for cancer research purposes –Researchers say one in 3trillion chance Covid developed the code naturally | 23 Feb 2022 | Fresh suspicion that Covid may have been tinkered with in a lab emerged today after scientists found genetic material owned by Moderna in the virus’s spike protein. They identified a tiny snippet of code that is identical to part of a gene patented by the vaccine maker three years before the pandemic. It was discovered in SARS-CoV-2’s unique furin cleavage site, the part that makes it so good at infecting people and separates it from other coronaviruses. The structure has been one of the focal points of debate about the virus’s origin, with some scientists claiming it could not have been acquired naturally… They claim there is a one-in-three-trillion chance Moderna’s sequence randomly appeared through natural evolution.
CLG News
Covid-19 was not made in 2019. It was made from the 19 nucleotide Moderna specific chimeric (CGG for AGA) furin cleavage site (in 2013) which does not occur anywhere in nature. And every Covid death and every Covid vaccine death is parked squarely on the doorstep of ModeRNA and The Covid19 makers, the genetic vaccine makers. their funders and their promoters, which include almost every government and public sector and health service in the world, are therefore guilty of Genocide and crimes against humanity. They have pushed genetic rape and sickness and death onto half of the population of the world in order to enrich the pockets of Pharmaceutical Companies. Governments and Public sectors around the world have abandoned their health service regulation to billionaires and heartless corporations (me: and to make we humans, Trans Humans and now, the vaccinated, without any human rights whatsoever = Elon Musk’s Neuralink brain chip – see below)
The Expose
NEXT:
Dr Ugur Sahin, the COVID-19 vaccine he designed for Pfizer was designed in just few hours in a single day (on a computer) on January 25, 2020. No other vaccine in history has been created and manufactured so quickly. Previously, the fastest vaccine ever developed took more than four years. co-founder of BioNTech Not only that, Pfizer Chairman (((Albert Bourla))) hasn’t gotten around to having his shot, or Dr Ugur Sahin, last I knew. And it went from laboratory straight into human arms without any animal testing first – mRNA never used in humans ever before – doesn’t that strike you as odd?
Me: So let’s put the above into some sort of “context”.
Obviously, no virus was present, when this vaccine was made on a computer and a Covid infection, was not the basis of the vaccine creation, in the first place.
Documents by Pfizer Show BioNTech Paid FDA $2,875,842.00 “Drug User Fee” for COVID-19 Vaccine Approval
Vaccine Impact
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Me: 2013-12-16 Application filed by Moderna Therapeutics Inc for Covid-19, at the same time as this: Since 2013, all people vaccinated with GM-modified mRNAs are legally trans-human and legally identified as trans-human and do not enjoy any human or other rights of a state – see below:
Covid-19 Patent Horrors
By Dr. Ariyana Love
In my latest interview with Stew Peter’s, we discussed how the “Covid-19 vaccine” ingredients listed in the patents, reveal that all these poisonous death shots are deleting genes and genetically modifying Humans for patentability.
GRAPHENE
The Hydrogel patent US8415325B2 is listed in the Moderna patent, here. Hydrogels are also mentioned in a second Moderna patent, here. Hydrogel is listed in the Johnson & Johnson patent, here. Hydrogels are made from Graphene Oxide. Nobody can deny the evidence that Graphene Oxide is in the shots.
GMO HUMANS
All the Covid-19 “vaccine” patents mention gene deletion. All the patents except one, mention “complimentary DNA” (cDNA). cDNA is a chimeric mRNA cocktail that’s being coded into Human cells using artificial genetic sequences in cross-species genomics.
According to the US Supreme Court ruling in 2013, altering Humans with cDNA makes them patent eligible. The court documents show that cDNA is made using modified bacterium and Supreme Court judges ruled it patent eligible. This means that a plant, animal or Human, could be patented and owned if first genetically modified with cDNA.
Mark Steele summarized it perfectly by stating:
In the US, the Supreme Court has ruled that vaccinated people worldwide are products, patented goods, according to US law, no longer human. Through a modified DNA or RNA vaccination, the mRNA vaccination, the person ceases to be human and becomes the OWNER of the holder of the modified GEN vaccination patent, because they have their own genome and are no longer “human” (without natural people), but “trans-human”, so a category that does not exist in Human Rights. The quality of a natural person and all related rights are lost. This applies worldwide and patents are subject to US law.
Since 2013, all people vaccinated with GM-modified mRNAs are legally trans-human and legally identified as trans-human and do not enjoy any human or other rights of a state, and this applies worldwide, because GEN-POINT technology patents are under US jurisdiction and law, where they were registered.”
See link here: https://ambassadorlove.wordpress.com/2021/12/08/covid-19-patent-horrors/
NEXT
Neuralink Experiments Kills 15th Monkey
Published on February 25, 2022
Written by activistpost.com
Elon Musk’s Neuralink brain chip has killed yet another monkey. Nonetheless, steps toward human testing forge forward. (Me: Trans Human?)
A total of 15 macaque monkeys out of 23 have died at U.C. Davis in a Neuralink-funded project titled “Development of a Large-Scale Brain-Machine Interface in Rhesus Macaques.” By now “the others may be dead too,” says Ryan Merkley, the director of research advocacy for the Physicians Committee For Responsible Medicine (PCRM).
In addition to monkeys, Musk’s company whose slogan is “breakthrough technology for the brain” has also implanted Bluetooth-enabled chips in pigs and sheep in order to connect and communicate with computers via a small receiver.
Veterinary records obtained by PCRM, a US non-profit that advocates alternatives to animal testing, describe monkeys picking at their cranial implants post-surgery only to be drugged. While the animals are ‘under,’ they are hooked up to “electrophysiology hardware” to make sure the electronics are working. Some monkeys used in this experiment underwent “multiple major survival surgical procedures,” in which as many as 10 craniotomies were performed on one animal.
The Nefariousness of Neuralink
Neuralink had a contractual agreement with the University of California Davis, receiving more than $1.4 million for their participation.
In response to a public records request by the doctors’ group, UC Davis withheld almost all documents, claiming it was in the “public interest” to do so.
Yes, because the truth will literally make you nauseous.
Brazen, audacious, and yet permitted.
This time around, however, the egregious violations include removing portions of the monkeys’ skulls and inserting electrodes in their brain. Additionally, to fill in ‘dead space,’ they used an “FDA-approved” “BioGlue” in an unapproved manner, killing at least two monkeys by destroying portions of their brains.
When I looked up what the eff this substance is, I learned its ‘glutaraldehyde’ and ‘bovine serum albumin’ that together supposedly make an excellent adhesive strength by creating strong protein cross-linking bonds.
Does anyone care that it causes tissue toxicity and shouldn’t come in contact with any nerves? Once you get the rubber stamp of approval, Merkley explains that the particulars are not scrutinized.
In addition to using toxic adhesive in the noggin (head), the monkeys were caged alone, had steel posts screwed to their skulls, and suffered “facial trauma” and seizures following brain implants. They experienced recurring infections at implant sites, whereupon they were dosed with an overabundance of antibiotic prescriptions.
In some cases, as a result of deteriorating health, Neuralink and U.C. Davis euthanized monkeys before they were even used in the planned experiment. That means, they killed them before they even got started.
Neuralink’s experiments are continuing – except now they’re operating in at least two private Neuralink facilities: one in Fremont, California, and one outside of Austin, Texas.
Coming Soon: Hackable Human Animals
Neuralink itself writes that “all novel medical devices and treatments must be tested in animals before they can be ethically trialed in humans.”
Yet despite this remark and the fact several monkeys have already died, Neuralink is moving toward testing their brain implants on humans.
Case in point: Neuralink is hunting to recruit a Clinical Trial Director to work closely with doctors, engineers, and welcome the “first Clinical Trial Participants!” (Note: the exclamation mark ❗️is theirs).
They are also hiring an Algorithms/DSP Engineer to “accelerate” pathways “to human-ready brain implants.” Literal Human Noggin/Head Hackers.
I assume there are several out there who would literally die to be one of the first associated with Elon Musk’s pioneering.
Dr. Yuval Noah Harari, Transhumanist and World Economic Forum (WEF) loyalist, recently informed us that “the days of free will are over” but that humans are now “hackable animals.”
Recall, it was under the Rona Regime that we openly became lab rats. In June 2020, in the face of the (fake) COVID-19 Hegelian-Esque emergency, a symposium was held to weigh the pros and cons of bypassing animal trials.
This was warp speed, baby.
“Although this looks promising for fast-tracking vaccine development, there is division among the scientific community about bypassing animal models before Phase I clinical trials. In addition, agencies like PETA are against using animals for research purposes. The question remains: Can vaccine research do without an animal model?”
Me: We are all animals on this planet, however our species is defined as Human, but vaccinated are no longer human, but trans human, with no human rights at all, as above.
As Merkley states, Musk prompted this technology as a way to help people with paralysis and Parkinson’s, but yet Musk also talks about a needed “symbiosis” between human brains and A.I.
This is because Musk, Harari, and other technocrats have warned that AI could trigger the next World War and those super-intelligent robots could dominate the world. In fact, Lieber designed the neural lace “to upgrade the human brain to be more competitive against A.I.”
Neuralink started with rodents and has graduated to primates. I would venture to guess that Neuralink has meddled with way more than 35 monkeys. Mankind is next. Arguably, we humans (trans humans) are already the monkeys.
See more here: activistpost.com
Principia Scientific
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Trans Humans: “They” know your name, where you live, your telephone number, they have your DNA and with modern DNA technologies, they can forecast what sort of a trans human you are and will be and if you are suitable for experimentation, or kill you off, when not suitable.
After Neuralink, your thoughts will be provided by a computer somewhere and “you won’t own anything and you will be happy” and you will probably be warehoused with other modified trans humans for whatever purpose they decide to put you to – no more kids – kids will be created to order in test tubes and modified to suit and the numbers of trans humans will be regulated by those in charge and that is very much it for humans and non humans from here on in – all of this within the next 2 years in all probability, if the vaccines don’t kill you first – so what you see today, won’t be here for you trans humans “tomorrow”.
Me: Which fits neatly in with globalists saving the planet from overcrowding by killing us, the planet empty of us humans and trans humans, for them.
You want to blame someone for this: Trump, Biden, your Politicians and Big Pharma, who thought they could get away scott free – so will they?
Reply
Richard Noakes
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Official Biochemical and Statistical Evidence 100% confirms Moderna created Covid-19
By The Exposé on March 3, 2022
Evidence has emerged which proves beyond a reasonable doubt that the pharmaceutical giant Moderna, the company that has made billions through the sale of an experimental Covid-19 injection, actually created the Covid-19 virus.
Covid-19 means: 19 nucleotide sequence and not 2019 at all.
On February 23 the Daily Mail ran an article showing that Moderna has patented the 19 base letter (nucleotide) sequence which codes for the Furin Cleavage site in Covid-19.
By a concerned reader
They cited a Paper by Scientists in India, Switzerland, Italy and the US (cautiously entitled: MSH3 Homology and Potential Recombination Link to SARS-CoV-2 Furin Cleavage Site) in which they calculated that the chances of a 19 nucleotide sequence patented by Moderna randomly appearing in Covid-19 in circumstances where it does not appear anywhere else in nature are 1 in 3 trillion.
Furthermore they did not merely apply for a patent on 2016 February 4 with US9587003B2: as reported in the Daily Mail. They actually applied on 2013 December 16 for 4 patents with US9149506B2, US9216205B2, US9255129B2, US9301993B2:as well.
So Moderna had developed the 19 nucleotide gene sequence containing the Furin Cleavage Site which gives Covid19 its infectivity to humans by patented gain of function research as early as 2013, 6 years before the Wuhan outbreak took place. Not 3 as reported in the Mail and virally elsewhere..
The Expose
Scientists find virus contains tiny chunk of DNA that matches sequence patented by Moderna THREE YEARS before pandemic began –Genetic match discovered in Covid’s unique furin cleavage site on spike protein –Matched genetic sequence patented by Moderna for cancer research purposes –Researchers say one in 3trillion chance Covid developed the code naturally | 23 Feb 2022 | Fresh suspicion that Covid may have been tinkered with in a lab emerged today after scientists found genetic material owned by Moderna in the virus’s spike protein. They identified a tiny snippet of code that is identical to part of a gene patented by the vaccine maker three years before the pandemic. It was discovered in SARS-CoV-2’s unique furin cleavage site, the part that makes it so good at infecting people and separates it from other coronaviruses. The structure has been one of the focal points of debate about the virus’s origin, with some scientists claiming it could not have been acquired naturally… They claim there is a one-in-three-trillion chance Moderna’s sequence randomly appeared through natural evolution.
CLG News
Covid-19 was not made in 2019. It was made from the 19 nucleotide Moderna specific chimeric (CGG for AGA) furin cleavage site (in 2013) which does not occur anywhere in nature. And every Covid death and every Covid vaccine death is parked squarely on the doorstep of ModeRNA and The Covid19 makers, the genetic vaccine makers. their funders and their promoters, which include almost every government and public sector and health service in the world, are therefore guilty of Genocide and crimes against humanity. They have pushed genetic rape and sickness and death onto half of the population of the world in order to enrich the pockets of Pharmaceutical Companies. Governments and Public sectors around the world have abandoned their health service regulation to billionaires and heartless corporations (me: and to make we humans, Trans Humans and now, the vaccinated, without any human rights whatsoever = Elon Musk’s Neuralink brain chip – see below)
The Expose
NEXT:
Dr Ugur Sahin, the COVID-19 vaccine he designed for Pfizer was designed in just few hours in a single day (on a computer) on January 25, 2020. No other vaccine in history has been created and manufactured so quickly. Previously, the fastest vaccine ever developed took more than four years. co-founder of BioNTech Not only that, Pfizer Chairman (((Albert Bourla))) hasn’t gotten around to having his shot, or Dr Ugur Sahin, last I knew. And it went from laboratory straight into human arms without any animal testing first – mRNA never used in humans ever before – doesn’t that strike you as odd?
Me: So let’s put the above into some sort of “context”.
Obviously, no virus was present, when this vaccine was made on a computer and a Covid infection, was not the basis of the vaccine creation, in the first place.
Documents by Pfizer Show BioNTech Paid FDA $2,875,842.00 “Drug User Fee” for COVID-19 Vaccine Approval
Vaccine Impact
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Me: 2013-12-16 Application filed by Moderna Therapeutics Inc for Covid-19, at the same time as this: Since 2013, all people vaccinated with GM-modified mRNAs are legally trans-human and legally identified as trans-human and do not enjoy any human or other rights of a state – see below:
Covid-19 Patent Horrors
By Dr. Ariyana Love
In my latest interview with Stew Peter’s, we discussed how the “Covid-19 vaccine” ingredients listed in the patents, reveal that all these poisonous death shots are deleting genes and genetically modifying Humans for patentability.
GRAPHENE
The Hydrogel patent US8415325B2 is listed in the Moderna patent, here. Hydrogels are also mentioned in a second Moderna patent, here. Hydrogel is listed in the Johnson & Johnson patent, here. Hydrogels are made from Graphene Oxide. Nobody can deny the evidence that Graphene Oxide is in the shots.
GMO HUMANS
All the Covid-19 “vaccine” patents mention gene deletion. All the patents except one, mention “complimentary DNA” (cDNA). cDNA is a chimeric mRNA cocktail that’s being coded into Human cells using artificial genetic sequences in cross-species genomics.
According to the US Supreme Court ruling in 2013, altering Humans with cDNA makes them patent eligible. The court documents show that cDNA is made using modified bacterium and Supreme Court judges ruled it patent eligible. This means that a plant, animal or Human, could be patented and owned if first genetically modified with cDNA.
Mark Steele summarized it perfectly by stating:
In the US, the Supreme Court has ruled that vaccinated people worldwide are products, patented goods, according to US law, no longer human. Through a modified DNA or RNA vaccination, the mRNA vaccination, the person ceases to be human and becomes the OWNER of the holder of the modified GEN vaccination patent, because they have their own genome and are no longer “human” (without natural people), but “trans-human”, so a category that does not exist in Human Rights. The quality of a natural person and all related rights are lost. This applies worldwide and patents are subject to US law.
Since 2013, all people vaccinated with GM-modified mRNAs are legally trans-human and legally identified as trans-human and do not enjoy any human or other rights of a state, and this applies worldwide, because GEN-POINT technology patents are under US jurisdiction and law, where they were registered.”
See link here: https://ambassadorlove.wordpress.com/2021/12/08/covid-19-patent-horrors/
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Neuralink Experiments Kills 15th Monkey
Published on February 25, 2022
Written by activistpost.com
Elon Musk’s Neuralink brain chip has killed yet another monkey. Nonetheless, steps toward human testing forge forward. (Me: Trans Human?)
A total of 15 macaque monkeys out of 23 have died at U.C. Davis in a Neuralink-funded project titled “Development of a Large-Scale Brain-Machine Interface in Rhesus Macaques.” By now “the others may be dead too,” says Ryan Merkley, the director of research advocacy for the Physicians Committee For Responsible Medicine (PCRM).
In addition to monkeys, Musk’s company whose slogan is “breakthrough technology for the brain” has also implanted Bluetooth-enabled chips in pigs and sheep in order to connect and communicate with computers via a small receiver.
Veterinary records obtained by PCRM, a US non-profit that advocates alternatives to animal testing, describe monkeys picking at their cranial implants post-surgery only to be drugged. While the animals are ‘under,’ they are hooked up to “electrophysiology hardware” to make sure the electronics are working. Some monkeys used in this experiment underwent “multiple major survival surgical procedures,” in which as many as 10 craniotomies were performed on one animal.
The Nefariousness of Neuralink
Neuralink had a contractual agreement with the University of California Davis, receiving more than $1.4 million for their participation.
In response to a public records request by the doctors’ group, UC Davis withheld almost all documents, claiming it was in the “public interest” to do so.
Yes, because the truth will literally make you nauseous.
Brazen, audacious, and yet permitted.
This time around, however, the egregious violations include removing portions of the monkeys’ skulls and inserting electrodes in their brain. Additionally, to fill in ‘dead space,’ they used an “FDA-approved” “BioGlue” in an unapproved manner, killing at least two monkeys by destroying portions of their brains.
When I looked up what the eff this substance is, I learned its ‘glutaraldehyde’ and ‘bovine serum albumin’ that together supposedly make an excellent adhesive strength by creating strong protein cross-linking bonds.
Does anyone care that it causes tissue toxicity and shouldn’t come in contact with any nerves? Once you get the rubber stamp of approval, Merkley explains that the particulars are not scrutinized.
In addition to using toxic adhesive in the noggin (head), the monkeys were caged alone, had steel posts screwed to their skulls, and suffered “facial trauma” and seizures following brain implants. They experienced recurring infections at implant sites, whereupon they were dosed with an overabundance of antibiotic prescriptions.
In some cases, as a result of deteriorating health, Neuralink and U.C. Davis euthanized monkeys before they were even used in the planned experiment. That means, they killed them before they even got started.
Neuralink’s experiments are continuing – except now they’re operating in at least two private Neuralink facilities: one in Fremont, California, and one outside of Austin, Texas.
Coming Soon: Hackable Human Animals
Neuralink itself writes that “all novel medical devices and treatments must be tested in animals before they can be ethically trialed in humans.”
Yet despite this remark and the fact several monkeys have already died, Neuralink is moving toward testing their brain implants on humans.
Case in point: Neuralink is hunting to recruit a Clinical Trial Director to work closely with doctors, engineers, and welcome the “first Clinical Trial Participants!” (Note: the exclamation mark ❗️is theirs).
They are also hiring an Algorithms/DSP Engineer to “accelerate” pathways “to human-ready brain implants.” Literal Human Noggin/Head Hackers.
I assume there are several out there who would literally die to be one of the first associated with Elon Musk’s pioneering.
Dr. Yuval Noah Harari, Transhumanist and World Economic Forum (WEF) loyalist, recently informed us that “the days of free will are over” but that humans are now “hackable animals.”
Recall, it was under the Rona Regime that we openly became lab rats. In June 2020, in the face of the (fake) COVID-19 Hegelian-Esque emergency, a symposium was held to weigh the pros and cons of bypassing animal trials.
This was warp speed, baby.
“Although this looks promising for fast-tracking vaccine development, there is division among the scientific community about bypassing animal models before Phase I clinical trials. In addition, agencies like PETA are against using animals for research purposes. The question remains: Can vaccine research do without an animal model?”
Me: We are all animals on this planet, however our species is defined as Human, but vaccinated are no longer human, but trans human, with no human rights at all, as above.
As Merkley states, Musk prompted this technology as a way to help people with paralysis and Parkinson’s, but yet Musk also talks about a needed “symbiosis” between human brains and A.I.
This is because Musk, Harari, and other technocrats have warned that AI could trigger the next World War and those super-intelligent robots could dominate the world. In fact, Lieber designed the neural lace “to upgrade the human brain to be more competitive against A.I.”
Neuralink started with rodents and has graduated to primates. I would venture to guess that Neuralink has meddled with way more than 35 monkeys. Mankind is next. Arguably, we humans (trans humans) are already the monkeys.
See more here: activistpost.com
Principia Scientific
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Trans Humans: “They” know your name, where you live, your telephone number, they have your DNA and with modern DNA technologies, they can forecast what sort of a trans human you are and will be and if you are suitable for experimentation, or kill you off, when not suitable.
After Neuralink, your thoughts will be provided by a computer somewhere and “you won’t own anything and you will be happy” and you will probably be warehoused with other modified trans humans for whatever purpose they decide to put you to – no more kids – kids will be created to order in test tubes and modified to suit and the numbers of trans humans will be regulated by those in charge and that is very much it for humans and non humans from here on in – all of this within the next 2 years in all probability, if the vaccines don’t kill you first – so what you see today, won’t be here for you trans humans “tomorrow”.
Me: Which fits neatly in with globalists saving the planet from overcrowding by killing us, the planet empty of us humans and trans humans, for them.
You want to blame someone for this: Trump, Biden, your Politicians and Big Pharma, who thought they could get away scott free – so will they?
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Lisa
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Thank you for putting that info up. Just wanted to note that copying references (here, and here) does not show up in your text, one has to go to the original.
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Robert Beatty
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I wonder what was ‘injected’ into all those leading citizens who lined up on tv to show how they lead from the front.
Unlikely to be the ‘real’ jab, maybe just a saline solution.
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Wisenox
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“Suzuki et al. (2021) went on to demonstrate experimentally that the S1 component of the SARS-CoV-2 virus … activated the MEK/ERK/MAPK signaling pathway to promote cell growth”
Activation of the MEK/ERK pathway is done by phosphorylation. In the brain, ERK phosphorylation will result in the activation of the STAT cascade, from which neural degeneration will occur.
“Excessive activation of upstream proteins and kinases in the ERK pathway has been shown to induce various diseases, including cancer, inflammation, developmental disorders and neurological disorders”.
https://www.spandidos-publications.com/10.3892/etm.2020.8454
The real question with the vaccine, is whether it is activating the MAPK p38 pathway, or bypassing it. P38 is responsible for apoptosis when things go bad:
“Each MAPK signalling cascade consists of at least three tiers: MAP3K, MAPKK and MAPK (3,6) (Fig. 1). Studies have shown that the JNK and p38 MAPK pathways are mainly related to stress and apoptosis of cells, while the ERK/MAPK signalling pathway, which is the most thoroughly studied MAPK signalling pathway, is closely related to cell proliferation and differentiation”
https://www.spandidos-publications.com/10.3892/etm.2020.8454
I have posted about this exact process occurring through wifi numerpus times on this site, with zero conversation elicited. That’s always blown my mind, as wifi is being overlooked as a major cause of illness, and also because this site is about actual science; one simply assumes that commentors align with the site because they post here.
Here’s an example showing 7.5Ghz doing the same:
“High-frequency EF enhanced capillary morphogenesis, VEGF release, MEK-cRaf complex formation, MEK and ERK phosphorylation, whereas no MAPK/JNK and MAPK/p38 pathways activation was observed.
The results provide evidence for a novel intracellular mechanism for EF regulation of endothelial angiogenic response via frequency-sensitive MAPK/ERK pathway activation”
https://royalsocietypublishing.org/doi/10.1098/rsif.2012.0548
That’s just one study, there are more frequencies shown to do the same thing. When they say wifi gives you covid, they may actually be right..
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coronistan.blogspot.com
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Unintended is of course fully intended
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