COVID-19 Vaccines May be the biggest "Uh-Oh" in History

The COVID-19 vaccine may be wreaking havoc in your body and why you should worry

Before I get into why the COVID-19 vaccines may be the biggest "uh-oh" in history, let's talk about how the vaccine functions. (If you wish to skip this part, go straight to "Spike Protein Problems" below)

I'll use Moderna as the example here and do my best to explain the action of the vaccine and how it is supposed to work.

How the Vaccine Works

The Moderna vaccine is an mRNA vaccine. In the simplest terms, it turns your cells into manufacturing facilities to produce the spike protein associated with COVID-19.

A decent analogy of this would be a 3D printer. For a 3D printer to function in our world, it needs a blueprint. The same is true for your cell's 3D printer, which I'll explain as simply as I can.

Inside our body, an original blueprint would be a gene (one segment of DNA). In the body, the 'printer' that makes blueprint copies from the original is called RNA Polymerase. This method allows your body to continually copy new blueprints (mRNA) from genes.

The mRNA then makes its way out of the nucleus and finds its way to the 3D printer (protein printer) called a ribosome. The ribosome produces protein in pairs of three nucleotides (called a codon). Once the mRNA has been fully translated, a protein is produced.

Because our DNA doesn't have genetic code for sequencing COVID-19 spike proteins (thank goodness), Moderna found a way to transport that blueprint copy (mRNA) into your cells. It does this using a lipid nanoparticle (think of the Amazon package dropped at your door - the contents of which is the mRNA but the box it's in is the nanoparticle). The nanoparticle is taken into the cell, where the mRNA (blueprint copy) is released.

The mRNA from the vaccine then makes its way to our cells' 3D printers (ribosomes), which then prints the "spike protein" that everyone has probably heard about.

Okay, so now we know how the vaccine works and what it produces. Let's talk about why this production may prove quite devastating to those receiving the vaccine, and any potential booster shot.

Spike Protein Problems

In a study published on March 31st, 2021, researchers produced a pseudovirus (or pseudospike) which consisted of only the spike protein and not a duplicating virus. If reading the study is confusing, please check out this 'layman's terms' article here: Scitechdaily.

What they found is quite scary, unfortunately. I'll quote from the article:

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.

"If you remove 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, the S protein receptor, now famous thanks to COVID," Manor explains. "Further studies with mutant spike proteins will also provide new insight towards the infectivity and severity of mutant SARS CoV-2 viruses."

What this shows is that the virus is merely a delivery mechanism of the most devastating aspect of COVID-19. Leading up to this study, scientists and researchers couldn't figure out why COVID-19 was destroying blood vessels.

This phenomenon, which resulted in wide-ranging symptoms and causes of death in people with COVID-19, was known, but the mechanism behind the 'why' was not.

Unfortunately for humanity, researchers were in such a hurry to produce a vaccine for this disease (it was sequenced in 2 days), that they used the Spike protein as the foreign body to induce an immune response. Perhaps they didn't realize the spike protein was the problem because they didn't let enough time pass before rushing out SOMETHING.

This is unfortunate because we NOW KNOW that the spike protein is actually the thing that is causing all of these problems in patients with COVID-19. The spike protein itself is resulting in mechanical issues within the body that leads to blood clots, low platelet counts, high D-Dimer concentration, and wide-ranging symptoms from brain issues to heart issues.

Doctors began seeing these problems early on and began theorizing that the spike protein itself, NOT just the virus, was at issue and begged the health agencies to reevaluate the safety of COVID-19 vaccines, but it did them no good.

Whether intentional, or due to knee-jerk reaction and lack of thought and understanding, it is becoming clearer and clearer that the vaccine is essentially injecting you with mRNA that produces the very spike protein that is the culprit in all the worst symptoms of COVID. It doesn't matter that the spike protein produced in your body isn't attached to a virus, because it is the reason COVID has been so devastating.

Now they are pushing for another booster shot, which could prove devastating to populations around the globe. With each shot, your body produces more of the spike protein, which results in more mini-blood clots, which cause wide-ranging health problems. These mini-clots go undetected, largely, and is likely the reason there are so many vaccination sufferers that are being turned away by doctors when no clots or other health problems are found. Mini clots don't show up on MRIs, etc. D-Dimer tests are needed, but aren't being utilized properly.

Sadly, any mention of this is being censored by everyone. Doctors who see this in their patients and report it publicly are being labeled as perpetuating misinformation. Their channels are being deleted, their warnings are being suppressed, and the ones that suffer are you and I.

But if you look hard enough, you'll find smatterings of truth revealed by the very people who continually cheerlead the safety of the vaccine, as you'll see in this study: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8084611/

A plausible explanation for the combination of thrombotic events and low blood platelets count (<150,000/microL), observed as serious adverse event, is the immune response ('immunothrombosis') [38] following vaccination, which resembles a condition similar to the heparin-induced thrombocytopenia (HIT) [39, 40]. These events could be related to vaccine-induced autoantibodies against a PF4 platelet antigen (vaccine-induced prothrombotic immune thrombocytopenia), a reaction occurring 4 to 20 days after vaccination. A positive HIT antibody suggests such diagnosis [39, 40]. Most of the cases from Europe have occurred in women under age 55.

Although these events were very rare, their incidence and the similar pattern across different individuals raised some concerns for a causality relation with vaccine. Besides, the pathogenesis of hypercoagulability after vaccination remains poorly understood. An enhanced immunological reaction mimicking active COVID-19 may be postulated. Indeed, immunothrombosis is a peculiar pathogenic mechanism in COVID-19. As suggested by Bonaventura and co-workers, SARS-CoV-2 infection induces the activation of neutrophils and monocytes which may interact with platelets and the coagulation cascade potentially leading to intravascular clot formation in small and larger vessels [38].

In layman's terms, they are confirming what I have just discussed, but they use terms like "poorly understood," and "rare" or say "some concerns for a causality relation with vaccine."

And then also this:

When a vaccinated cell dies or is destroyed by the immune system, the debris may release a large amount of Spike proteins and protein fragments (free-floating Spike proteins).

It is well known that SARS-CoV-2 uses ACE2 as a Trojan horse to invade target cells. Thus, interactions between free-floating Spike proteins and ACE2 of other cells are highly plausible mechanisms. As recently demonstrated for adenovirus-vectored vaccines, Spike proteins produced upon vaccination have the native-like mimicry of SARS-CoV-2 Spike protein's receptor binding functionality and prefusion structure [41].

The native-like conformation of the Spike protein produced by vaccines has the potential to interact with ACE2, promote ACE2 internalization, and its degradation [42]. Of note, such phenomenon has been also observed in platelets [43]. Zhang and co-workers found that SARS-CoV-2 induced a time-dependent decrease in ACE2 levels in platelets, indicating the degradation of ACE2 upon ACE2 activation [43]. Spike protein induces a dose-dependent enhancement of platelet aggregation and adenosine triphosphate (ATP) release [43]. The subuni 1 of the Spike protein, but not subunit 2, is that binds to ACE2 of platelets thereby triggering platelet aggregation (Fig. 2 ) [43].

Unfortunately for them, the mistake has already been made and it is unlikely they will, any time soon, admit that they realized the mistake and either found a new method of producing immune response that has nothing to do with the spike protein, or stopping the vaccines altogether.

This is why it's so important that you do your due diligence and take everything the "experts" tell you with a grain of salt. Accepting experimental 'vaccines' that are produced with a snap of a finger is more likely to cause an "Uh-oh" moment across the globe.

Or, perhaps, they knew exactly what was wrong and did this on purpose. But I'll let the conspiracy theorists sort that one out.