Oh.

So for a while now I’ve been discussing the lab-created SARS-CoV-2 virus, especially its spike protein, which alone, I’ve claimed, is pathogenic (30%).

The mainstream press and the regulatory and healthcare bureaucracies in the US and other parts of the world have said otherwise. More, they’ve assured you that the code injected in vaccines to make the spike protein is short lived and remains at the injection site.

Neither of these claims, enforced by the “Trusted News Initiative” as the only credible information that you’re allowed to see on social media platforms, is correct; you’ve been lied to.

Per Ogata et al, the spike protein can circulate in your body for 2 weeks post vaccination. Another study has revealed spike protein remnants found in the body 15 months and counting after exposure.

The spike proteins break off and disperses throughout the body. Where they settle and how they replicate can determine harm. Pfizer was asked by Japan to do a bio-distribution study, which showed dispersal of the Lipid-Nano-Particle delivery system for the coded mRNA all over the body, with the ovaries most susceptible. The goal of treating the virus early with non-mutagenic anti-virals, a competitive binding agent (ivermectin), an ionophore (HCQ), and something like zinc that disrupts RNA replication in the cells, is to greatly reduce the viral load and prevent the spike protein from moving into your respiratory tract, where it causes inflammation and, when circulating through your blood cells, later creates micro-clotting issues. The same can be said for monoclonal antibodies, which have proven so successful that our government has pulled them back, creating an artificial shortage. First and foremost, for whatever the reason, they want a needle in your arm.

The mRNA and adenovirus vaccines — designed to teach your body to make the spike protein — create non-sterilizing antibodies against all but the Wuhan strain, which is the spike the vaccine was designed around, but is no longer extant. These are binding antibodies, not neutralizing antibodies like the kind you’d find in a non-leaky vaccine. This would explain the initial effectiveness of the vaccines; that they wane, and that they are unable to defend against certain variants, make them susceptible to adverse events.

Binding antibodies can actually help the virus into the body — which may explain the significantly higher viral loads in Delta vs the viral loads pre-vaccine. It may also suggest that the equal or higher viral loads in the vaccinated are impacting the unvaccinated, rather than the other way around, as we’d expect in cases of evolutionary pressure creating antigen escape: we followed a treatment path that resulted in a contagious variant with the mutation profile to defeat the vaccines. This has insured that the Delta variant is being passed around.

That the vaccines seem to re-orient the immune system is also troubling.

Pace Joe Biden and the healthcare bureaucrats, this is a pandemic of the vaccinated.

From “Pathogenic antibodies induced by spike proteins of COVID-19 and SARS-CoV viruses” [pre-print]:

“Binding of pathogenic antibodies to human healthy tissues”

As more evidence of the pathogenicity of the pathogenic anti-COVID-19 S1 antibodies, REGN10987 and mutiple healthy human tissues from a tissue array slide (US Biomax, FDA999w) were used to further evaluate the pathogenicity of REGN10987. The tissue array slide was comprised of 32 types of normal human organs encompassing most of human tissues, representing FDA guidelines for antibody cross-reactivity testing. The results showed that REGN10987 bound significantly to human healthy tissues of lung, kidney, pancreas, stomach, intestine, adrenal gland, peripheral nerve, thyroid gland, spleen, adenohypophysis, testicle, prostate, bone marrow, uterine cervix of cancer adjancent normal tissue (Figure 7). In addition, REGN10987 also bound to the tissues of parathyroid gland, pericardial mesothelium, and adjacent normal sclera of eye (data not shown). The data indicate that certain anti-COVID-19 S1 antibodies, such as REGN10987, are highly pathogenic because it has the high potential to bind to healthy human tissues, activating self-attacking immune responses (ADAA) and inducing serious adverse reactions in vivo. Based on the results, clinical detection of pathogenic antibodies during the COVID-19 infection may be helpful in predicting the consequences of a patient with a serious infection.

Figure 7: Binding of the REGN10987 to various normal human tissues.

Taken together, the in vitro and in vivo data of the current study revealed that certain pathogenic antibodies specific to the COVID-19 spike protein can be the cause of a serious COVID-19 infection, and can cause serious complications during COVID-19 infections through ADAA. Further, the pathogenic antibodies can bind to unmatured fetal cells or tissues and cause abortions, postpartum labors, still births, and neonatal deaths of pregnant females.

Given the pathogenicity of the spike protein, early treatment designed to prevent spike protein from propagating seems far wiser, from the standpoint of treatment and prevention, than injecting code into the body instructing it to make the pathogen and disperse it over the body. We know that the spike can traverse the blood-brain barrier. How much of the spike is made seems to vary on an individual basis; but that can also be potentially tied to dosing.

Keep in mind that under the EUA, the pharmaceutical companies making these vaccines are permitted to change dosages, etc., without having to disclose any changes publicly. Is the reason some people are dying from the vaccine, some are being permanently injured, and others have no adverse events — save for having taken a vaccine that doesn’t prevent future infection — tied to dosing and placebo?

There is so much we don’t yet know, and the suppression of information is one of the reasons why many are so distrustful of this universal vaccine campaign.

The ADAA (self-attacking immune responses) noted in this study was predicted by several world-renowned scientists, one with a Nobel Prize for the discovery of HIV, who have been virtually banished from social media and are being blacklisted by major medical journals. This includes the inventor and patentor of mRNA gene-transfer technology, Dr Robert Malone. This effect was also a constant in mRNA vaccine studies in animals, leading to the majority of the animals dying.

What we’ve set in motion here is a potential genocidal event. A more virulent variant (should one emerge as dominant), combined with the binding antibodies in the mass vaccinated, could create the conditions for an unstoppable super-virus. At that point, we’d have to hope that catching Delta while vaccinated provides those who recover with the naturally-acquired immunity granted the Covid-recovered who have remained unvaccinated. Sadly, we now know that the Covid-recovered actually lose immune durability with subsequent vaccinations, and are at a greater risk of an adverse event. A vaccine provides no additional protections.

Hubris kills.

Source: https://proteinwisdom.com/?p=58889