In 2021, Bill Gates balked and denied that the so-called vaccines were being used to deliver microchips to track unsuspecting humans. “It makes no sense technologically,” he said. “And even if it was possible, why would I be involved with that? I don’t get it.”
Sure. You don’t get it.. Of course.
Ironically, nano lipids – also small and undetectable like microchips – are more than capable to be used as tracking mechanisms in both humans and animals. And they ARE being used for this purpose. Gates, however, has no issues with these applied sciences and has in fact advocated and invested in ‘detection technologies’ as early as 2017. The nanomedicine market, by the way, is predicted to reach over $164 billion by 2027.
And Gates is not alone – Big Pharma Technocrats will tell you that “the success of mRNA vaccines would not have been possible without the lipid nanoparticles (LNPs).” In reality, these LNPs are the lynchpins that “protect” mRNA and deliver it into our cells where it can circulate throughout the body.
Unlike a traditional vaccine that has an inactivated virus injected in order to stimulate an antibody response, the COVID injection is completely different in this respect. It uses messenger RNA (mRNA), which is a blueprint for your cells to create COVID-like (spike) proteins. Then your cells begin to make these COVID-like proteins.
The LNP was chosen as a carrier vehicle to protect the mRNA from degradation and to aid intracellular delivery and endosomal escape. The role of lipid nanoparticles in connection with the mRNA vaccines from Moderna and Pfizer–BioNTech has not been highlighted enough; neither has the havoc NLPs create.
To put it into perspective, if it weren’t for these lipids, the mRNA wouldn’t be able to successfully turn the jabbed people into miniature spike protein producing factories. The lipid enables the mRNA payload. It allows Big Harma complete access to your cells.
As replication occurs, an immune response is triggered, which can express itself in a myriad of ways. To get an idea, you can peruse the nine pages of 1,291 adverse side effects that Pfizer tried to hide from the people for 75 years. How do we know that? Because Pfizer listed these events in their own safety report from the phase 1/2 trials.
Before we get into the warped “perks” of lipids, there are many aspects to this ‘jab juice from hell’. The NLP is just one such particular component. Based on thousands of hours of research over three-plus years, I firmly believe the release of these injections involved different experiments all over the world where different variations of G.O., lipids, mRNA, Spike, and nanotech were tested. (Remember, we needed really cold temps and freezer pharms at first, which is needed to preserve nanotech. So what happened with those?)
Inflammation (In Nano) Now A Good Thing!
Liposomes are incredible things. Discovered in 1965, they consist of closed lipid bilayer vesicles that spontaneously self-assemble in water to form fatty capsules. They offer a clever way to sneak something into a cell. Of course like with all things Big Pharma, scientists worked to synthesize nature. Today, lipid nanoparticles (LNPs) have emerged across the pharmaceutical industry as promising vehicles to deliver a variety of therapeutic agents.
The LNPs in the Rona jab juice from Pfizer and Moderna are a crafted concoction of pharmaceia (sorcery). The nano lipids alone consist of a mixture of phospholipids, cholesterol, PEGylated lipids, and cationic or ionizable lipids. The phospholipids and cholesterol have structural and stabilizing roles, whereas the PEGylated lipids support prolonged circulation. The cationic/ionizable lipids are included to allow the complexing of the negatively charged mRNA molecules and enable the exit of the mRNA from the endosome to the cytosol for translation.
Pfizer and Moderna source out this component for their ‘vaccines’ – meaning they purchase lipid nanotechnology from Acuitas, a Vancouver-based company founded in February 2009 that partners with multiple pharmaceutical companies, biotechnology companies, and academic institutes to advance nucleic acid therapeutics.
Their website boasts,
“Recent achievements include the use of its LNP delivery system in the Pfizer/BioNTech COVID-19 vaccine COMIRNATY® that is being administered around the world. This success resulted in the recently announced partnership with Pfizer that enables the American multinational pharmaceutical company to use Acuitas Therapeutics’ LNP technology for up to 10 targets for vaccine or therapeutic development. …. The team continues its work with partners to address serious illnesses and diseases such as HIV/AIDS, cancer, tuberculosis, malaria, and more.
Just one small detail – Acuitas’ LNPs used in preclinical nucleoside-modified mRNA vaccine studies were highly inflammatory in mice. This stuff is now going into humans.
The mice “…showed clinical signs of piloerection, hunched body, decreased activity, and irregular respiration. This might indicate toxicity of the LNP formulation at high doses.” The same dose of LNP delivered intranasally led to similar inflammatory responses in the lung and resulted in a high mortality rate, with the mechanism unresolved.
Unresolved?
They concluded that the “mRNA-LNP platforms” potency in supporting the induction of adaptive immune responses and the observed side effects may stem from the LNPs’ highly inflammatory nature.”
Is it a surprise that this foreign substance injected or inhaled may trigger inflammation?
Is this a new normal? Sadly, it’s not. Prompting an immune response by exposing a human to foreign toxic substances has been the usual. Think about all the poisonous adjuvants in vaccines. What is even more alarming is that the potentially inflammatory nature of these LNPs was not assessed. Not really.
While researchers adjusted the levels for humans, they outlined that further studies were needed to determine the exact nature of the inflammatory responses triggered by mRNA-LNP vaccines in humans, and how much overlap there might be with the inflammatory signatures documented in mice.
We’ve known for a long time that cationic lipid coating of mRNA is toxic. They are attracted to and are destructive toward:
- lungs
- mitochondria
- red and white blood cells
- liver
- immune and nervous systems function
Some studies remarked that there was a very good chance that the mRNA-LNP platform crosses the blood-brain barrier and reaches the central nervous system (CNS). In other instances, it was shown that indeed intranasally inoculated nanoparticles readily enter the CNS, and this is the “preferred method to overcome the blood-brain barrier and deliver active substances to the brain.”
Pfizer et al. Knew All Along
Weeks ago, I was one of the first to tweet leaked files obtained under the Freedom of Information Act. The documents revealed that Australia’s Pharma Regulator TGA suppressed a troubling report about Pfizer’s COVID-19 “vaccine.” Pfizer knew that lipid nanoparticles go everywhere once in the body. Their mRNA encoding LUCIFERASE was able to track where the teeny tiny nanoparticles go –not only in the liver and ovaries and brain, but in the bone marrow and heart. They claimed that the synthetic ionizable lipid cleared from the body in nine days, but other accounts show the nanoparticles having approximately 20–30 days of half-life.
Australia’s government wasn’t alone. Most governments knew as early as the beginning of 2021 that these jabs were dangerous and that the nanolipids spread in the body. Why didn’t they act with an abundance of caution???
These jabs should have never been released onto the market. Technically, studies were still ongoing. Why didn’t they release the study data at the time? Isn’t this a violation of informed consent?
This is concerning, but not surprising in The Age of Covid. This is a good time to inform readers that Ray Kurzweil outlined that the singularity is near. He says straight up that the nano will replace the human cell. “With the advent of full-scale nanotechnology in the 2020s, we will have the potential to replace biology’s genetic information repository in the cell nucleus with a nanoengineered system…”
Silent Blatant Culling Rages On
Recently, I had an ex-boyfriend tell me this P*andemic is over. But is it? #Covidisntover was just trending and it’s April 2023. The wreckage is still being assessed. Some would argue that we’re just getting started with this transhumanist agenda.
At 45, he had never taken a vaccine before, which contributed to his robust immune system. Perhaps he was in an easier place to play Russian Roulette with his life, which he did in order to go do a TV show in Canada. In any case, he took J&J’s old-school live attenuated one-prick-and-you’re-done shot. He is fine and was adamant that vaccine injuries are akin to reacting to eating a peanut. “A peanut can kill you, but it’s not inherently the peanut.”
He then even questioned my mom’s gallbladder failure a week after her second Pfizer shot. How do you know it was the vaccine? he asked. I didn’t argue back, although gallbladder failure with the Pfizer shot is a thing.
I’ve been covering vaccine safety since 2012, and I’ve never come across so many vaccine-injured people. I listen to vaccine-injured testimonials on Twitter Spaces. I make myself sit on six-hour FDA and CDC hearings and read patents and studies every single day. And, may I add, I’ve personally interviewed hundreds of those who have been damaged and/or have lost loved ones due to the Covid-19 injections.
Quietly, just this week, the government removed approval from the AstraZeneca Covid-19 vaccine, because of its side effects. Meanwhile, government officials in the UK officially recorded in documents that 70% of the people in the UK who have died in the last year have been double jabbed. That’s 7 out of 10 people! Remember this is a fact, not a conspiracy theory.