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The CDC Lied: The mRNA Wasn’t Meant to “Stay in the Arm”

By Robert Kogon | Brownstone Institute | February 10, 2023

The CDC’s information page on Covid-19 vaccines contains the following bullet points on “How mRNA COVID-19 vaccines work:”

First, mRNA COVID-19 vaccines are given in the upper arm muscle or upper thigh, depending on the age of who is getting vaccinated.

After vaccination, the mRNA will enter the muscle cells. Once inside, they use the cells’ machinery to produce a harmless piece of what is called the spike protein…. After the protein piece is made, our cells break down the mRNA and remove it, leaving the body as waste.

Or, in other words, as we have long been told, “it” – the mRNA – “stays in the arm.” And then, after having instructed the muscle cells to produce the spike, is disposed of.

But look at the below picture from a recent presentation on mRNA vaccination at the European Parliament. The picture was posted on Twitter by Virginie Joron, a French member of the parliament. The speaker is no less an authority than Özlem Türeci, the Chief Medical Officer of BioNTech: the German biotech company that developed what has come to be known to most of the world as the “Pfizer” Covid-19 vaccine.

Have a closer look at Türeci’s slide, which tells a very different story than that which the CDC has been telling Americans for the last two years.

Far from “staying in the arm” and entering the muscle cells at the injection site, the injection site is only the point of departure for a journey that is supposed to take the mRNA rather to the lymph nodes. The subtitle of the slide is “Bringing mRNA to the right cells at the right places.” The deltoid is not the right place; the lymph nodes are.

Once in the lymph nodes, a specific sort of cell, the dendritic cells, is supposed to manufacture the spike protein: here colorfully described as the “wanted poster” that will help the immune system to identify the SARS-CoV-2 virus in case of subsequent exposure.

A passage from The Vaccine, the book that Türeci and her husband, BioNTech CEO Ugur Sahin, wrote which journalist Joe Miller, explains why BioNTech’s platform specifically targets the lymph nodes:

What Ugur learnt was that the location to which a vaccine delivers its ‘wanted poster’ really mattered. The reason for this, the couple’s team in Mainz later realised, was that not all dendritic cells … were created equal. The ones that resided in lymph nodes – of which the spleen is the largest – were particularly adept at capturing mRNA and making sure the instructions it carried were acted upon. These kidney-bean shaped organs, found under our armpits, in our groins, and at several other outposts in the body, are the information hubs of the immune system. (p. 98)

Indeed, Sahin and Türeci were so determined to get their mRNA into the lymph nodes that they had an earlier mRNA construct injected directly into the patient’s lymph nodes in the groin (p. 104).

Needless to say, such an approach was not likely to obtain wide acceptance as a vaccine! This is why the couple, as explained in their book, needed to package the mRNA in lipid nanoparticles, in order to ensure that mRNA administered by way of an intramuscular injection would, nonetheless, be widely distributed around the body and thus reach the lymph nodes.

This is to say that the wide biodistribution of the mRNA that came to light after rollout was never a bug. It is a feature of BioNTech’s mRNA technology. Having elicited an immune response by way of injection into the groin, Sahin is even said to have wondered, “How substantial could the immune response be if a vaccine got into all lymphatic tissues around the body, and recruited all the resident DCs [dendritic cells] into action?” (p. 105)

So, why has the CDC been lying about this for the last two years and insisting that the mRNA “stays in the arm?” Well, the obvious answer is that the idea of the mRNA staying at the injection site is reassuring, since otherwise we could fear systemic adverse effects of precisely the sort that have emerged since rollout.

It is worth noting, moreover, that in developing its vaccine, as discussed in my earlier article here, BioNTech simply skipped the so-called safety pharmacology studies whose purpose is precisely to test a candidate vaccine for potential systemic adverse effects – and regulators, including the FDA, let the company do it.

Robert Kogon is a pen name for a widely-published financial journalist, a translator, and researcher working in Europe.Follow him at Twitter here. He writes at edv1694.substack.com.

February 11, 2023 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular | , , , | 3 Comments

You cannot be forced to get the Covid vaccine. Here is the way out.

By Meryl Nass, MD | August 26, 2021

Let me show you how FDA, Pfizer and BioNTech colluded to fool everyone about the EUA status of the vaccine Americans will be offered. But close reading of their document gives you an escape route.

The “Fact Sheet for Recipients, “dated August 23, 2021, is approved by FDA and is on FDA’s website, and is signed by BioNTech and Pfizer.

Direct quotes from this easy to read 8 page document are below, and I suggest you print the document out, as it will help you avoid a vaccine mandate. Pay close attention. I added numbers to the most interesting excerpts.

After stating that you might receive the licensed vaccine or a vaccine under EUA in item 2, item 6 indicates that both the licensed vaccine AND the EUA vaccine are both under EUA. (This may be the way chosen to shield the licensed vaccine from liability.) Item 5 says that while under EUA, it is your choice whether or not to receive the vaccine.

Show this document to your college, your hospital, your boss. They cannot force you to receive either of these vaccines!

—————–

1.  The FDA-approved COMIRNATY (COVID-19 Vaccine, mRNA) and the FDA-authorized Pfizer-BioNTech COVID-19 Vaccine under Emergency Use Authorization (EUA) have the same formulation and can be used interchangeably to provide the COVID-19 vaccination series.[1]

2. You are being offered either COMIRNATY (COVID-19 Vaccine, mRNA) or the Pfizer-BioNTech COVID-19 Vaccine to prevent Coronavirus Disease 2019 (COVID-19) caused by SARS-CoV-2.

3. The licensed vaccine has the same formulation as the EUA-authorized vaccine and the products can be used interchangeably to provide the vaccination series without presenting any safety or effectiveness concerns. The products are legally distinct with certain differences that do not impact safety or effectiveness.

4. WHAT IF I DECIDE NOT TO GET COMIRNATY (COVID-19 VACCINE, mRNA) OR THE PFIZER-BIONTECH COVID-19 VACCINE?

5. Under the EUA, it is your choice to receive or not receive the vaccine. Should you decide not to receive it, it will not change your standard medical care.

6. This EUA for the Pfizer-BioNTech COVID-19 Vaccine and COMIRNATY will end when the Secretary of HHS determines that the circumstances justifying the EUA no longer exist or when there is a change in the approval status of the product such that an EUA is no longer needed.

Manufactured by Pfizer Inc., New York, NY 10017

Manufactured for BioNTech Manufacturing GmbH An der Goldgrube 12 55131 Mainz, Germany LAB-1451-7.2 Revised: 23 August 2021

August 27, 2021 Posted by | Civil Liberties, Deception | , , , , , | 2 Comments

And We Should Trust ‘The Science’ of the Pharma Industry?

By F. William Engdahl – New Eastern Outlook – 29.07.2021

The forever-head of the US NIAID, Tony Fauci, has repeatedly demanded that the public “trust the science” as he shifts his own science opinion from one positon to another. What is never mentioned in mainstream media in the West or almost anywhere in the world is the scientific record of the major global vaccine making pharmaceutical giants. In short, it is abysmal and alarming in the extreme. That alone should prohibit governments from pushing radical untested experimental injections on their populations without extensive long-term animal and other testing to assure their safety.

This past April as the US vaccination program was in high gear, the Biden chief covid adviser, 80-year-old Fauci, head of the National Institute of Allergy and Infectious Disease (NIAID) since 1984, announced that the US Centers for Disease Control (CDC) and the Food and Drug Administration (FDA) had decided to order a “pause” on giving the Johnson & Johnson (Janssen) vaccine in order to examine reports of blood clots. It turned out that there were six reported blood clot cases of some seven million who then had had the J&J covid jab. Fauci in his press remarks declared, “one of the things that’s, I think, such a good thing about our system here, is that we’re ruled by the science, not by any other consideration.” There is good reason to question Fauci.

That was supposed to reassure people that the authorities were being ultra-careful with the experimental covid medications which, after all, never have been mass-tested on humans before and have only gotten “emergency use authorization,” provisional FDA approval. The FDA quickly lifted the pause as J&J agreed to print that its vaccine could cause blood clots.

Yet at the same time, rival vaccine makers, Pfizer and Moderna, both using a hyper-experimental genetic treatment known as mRNA, were not being paused by “the science” despite the fact that hundreds of thousands of alarming vaccine-related severe reactions, including official data of several thousand deaths from both, had been recorded by CDC data base, VAERS (Vaccine Adverse Event Reporting System).

According to the CDC such “adverse” events, post-vaccine, include anaphylaxis, thrombosis with thrombocytopenia syndrome, Guillain-Barre Syndrome, myocarditis, pericarditis, and death. For the week of July 16 the CDC VAERS reported an alarming 9,125 reported deaths since late December from the COVID-19 vaccinations. Never in history have such high death totals been associated with any vaccine, yet the media is deafeningly silent about this.

Their dismal science record

The wording of Fauci is precise and deliberately manipulative. It suggests that there exists some fixed thing we can call “The Science,” like some Vatican religious dogma, whereas the real scientific method is one of continuous questioning, overturning past hypotheses with newly proven ones, adjusting. Yet when it comes to “Science,” the handful of giant vaccine makers, sometimes known as Big Pharma, a cartel not unlike Big Oil, have a record of fraud, deliberate doctoring of their own tests, as well as widespread bribing of doctors and medical officials to promote their various drugs despite “Science” results that contradict their assertions of safety. A look at the major global pharmaceutical giants is instructive.

J&J

We begin with the Johnson & Johnson Company of New Jersey. On July 21, 2021 J&J and three other smaller drug makers agreed to pay a staggering $26 billion damages to a group of US states for their role in causing America’s opioid epidemic. Of that J&J will pay $5 billion. The CDC estimates that use of the highly-addictive opioids as painkillers caused at least 500,000 deaths between 1999 and 2019. Johnson & Johnson is accused of pushing the deadly painkillers for excessive use and downplaying their addiction risks. They knew better.

The same J&J is in a huge legal battle for knowingly using a carcinogen in its famous baby powder. A 2018 Reuters investigation found J&J knew for decades that asbestos, a known carcinogen, lurked in its baby powder and other cosmetic talc products. The company is reportedly considering legally splitting its baby powder division into a small separate company that would then declare bankruptcy to avoid large payouts. The J&J covid vaccine, unlike that from Pfizer and Moderna, does not use mRNA genetic alteration.

The two global covid vaccine makers which have by far the largest market to date are the two being personally promoted by Fauci. These are from Pfizer in alliance with the tiny German BioNTech company under the name Comirnaty, and from the US biotech Moderna.

Pfizer

Pfizer, one of the world’s largest vaccine makers by sales, was founded in 1849 in the USA. It also has one of the most criminal records of fraud, corruption, falsification and proven damage. A 2010 Canadian study noted, “Pfizer has been a “habitual offender,” persistently engaging in illegal and corrupt marketing practices, bribing physicians and suppressing adverse trial results.” That’s serious. Note that Pfizer has yet to make fully public details of its covid vaccine studies for external examination.

The list of Pfizer crimes has gotten longer since 2010. It is currently engaged in lawsuits related to charges its Zantac heartburn medication is contaminated with a cancer-causing substance. As well, Pfizer received the biggest drug-related fine in US history in 2009 as part of a $2.3 Billion plea deal for mis-promoting medicines Bextra and Celebrex and paying kickbacks to compliant doctors. Pfizer pleaded guilty to the felony of marketing four drugs including Bextra “with the intent to defraud or mislead.” They were forced to withdraw their arthritis painkiller Bextra in the USA and EU for causing heart attacks, strokes, and serious skin disease.

Clearly in a move to boost revenue, Pfizer illegally paid doctors kickbacks for “off-label” use of more than one of its drug which resulted in patients being injured or killed. Among them were Bextra (valdecoxib); Geodon (ziprasidone HCl), an atypical antipsychotic; Zyvox (linezolid), an antibiotic; Lyrica (pregabalin), a seizure medication; its famous Viagra (sildenafil), an erectile dysfunction drug; and Lipitor (atorvastatin), a cholesterol drug.

In another court trial, Pfizer subsidiaries were forced to pay $142 million and release company documents that showed it was illegally marketing gabapentin for off-label use. “Data revealed in a string of U.S. lawsuits indicates the drug was promoted by the drug company as a treatment for pain, migraines and bipolar disorder – even though it wasn’t effective in treating these conditions and was actually toxic in certain cases, according to the Therapeutics Initiative, an independent drug research group at the University of British Columbia. The trials forced the company to release all of its studies on the drug, including the ones it kept hidden.”

In 2004 Pfizer subsidiary Warner-Lambert was forced to pay $430 to settle criminal charges and civil liability arising from its fraudulent marketing practices with respect to Neurontin, its brand for the drug gabapentin. Originally developed for the treatment of epilepsy, Neurontin was illegally promoted off-label for the treatment of neurological pain, and in particular for migraine and bipolar disorder – even though it wasn’t effective in treating these conditions and was actually toxic in some cases. Neurontin for unapproved uses made up some 90% of the $2.7 billion in sales in 2003.

A New York Times report disclosed in 2010 that Pfizer “… paid about $20 million to 4,500 doctors and other medical professionals in the United States for consulting and speaking on its behalf in the last six months of 2009.” It paid another $15.3 million to 250 academic medical centers and other research groups for clinical trials. In the US legal practice it is seldom that corporate executives actually doing the criminal deeds are prosecuted. The result is that court fines can be treated as “business costs” in this cynical milieu. In eight years of repeated malfeasance through 2009, Pfizer accumulated just under $3 billion in fines and civil penalties, about a third of one year’s net revenues.

In 2020 as its covid vaccine was in development, Pfizer paid $13,150,000 in lobbying Congress and officials in Washington among others. Also notable is the fact that the Bill and Melinda Gates Foundation own shares of both Pfizer and their partner in the leading mRNA vaccine, BioNTech of Germany.

Moderna

The third covid vaccine producer today with FDA Emergency Use Authorization (EUA) is Moderna of Cambridge, Massachusetts. It has yet to be sued for illegal practices unlike J&J or Pfizer. But that fact is likely only because before its EUA for its mRNA experimental vaccine, in its ten years existence since 2010 it had failed to get FDA approval to market a single medicine, despite repeated failed attempts. However Moderna has a red neon sign that reads “conflict of interest” that should give pause.

Moderna and Fauci’s NIAID have collaborated on development of vaccines using Moderna’s mRNA platform and NIAID of Fauci on coronaviruses including MERS, since at least November, 2015. On January 13, 2020, before the first case of a supposed Wuhan, China “novel coronavirus” was even detected in the United States, Fauci’s NIAID and Moderna signed an updated cooperation agreement which described them as co-owners of a mRNA based coronavirus and that they had finalized a sequence for mRNA-1273, the vaccine now being given to millions for supposedly averting the novel coronavirus. That means that Fauci’s NIAID and perhaps Fauci personally (it’s allowed in the US) stood to reap huge financial benefits from emergency approval of the Moderna jab, yet Fauci has never admitted to the conflict publicly when he was Trump corona adviser, nor as Biden’s.

Ten days later on January 23, 2020 Moderna announced it was granted funding by CEPI, a vaccine fund created by Bill Gates’ foundation along with Davos WEF among others, to develop an mRNA vaccine for the Wuhan virus.

Moderna was created by a venture capitalist, Noubar Afeyan along with Harvard professor Timothy A. Springer, and others. In 2011 Afeyan recruited French businessman and former Eli Lilly executive Stephane Bancel as CEO of the new Moderna. Despite having no medical or science degree nor any experience running a drug development operation, Bancel lists himself as co-patent holder for a hundred patents of Moderna tied to the different vaccines. Beginning in 2013 the tiny Moderna was receiving grants from the Pentagon to develop its mRNA technology. As of 2020 just prior to its receiving emergency use authorization from the US Government FDA, fully 89% of Moderna revenues were from US Government grants. This is hardly an experienced company yet it holds the fate of millions in its hands. As Fauci says, “Trust the Science.”

In February 2016, an editorial in Nature magazine criticized Moderna for not publishing any peer-reviewed papers on its technology, unlike most other emerging and established biotech companies. The company remains ultra-secretive. That same year, 2016 Moderna got $20 million from the Gates Foundation for vaccine development using mRNA.

Up to its receiving EUA approval for its covid mRNA product in December 2020 Moderna had only made losses since its founding. Then curiously, following a March 2020 personal meeting with then-President Trump where Bancel told the president Moderna could have a vaccine ready in a matter of months Moderna luck changed.

On May 15, Trump announced creation of Operation Warp Seed to rollout a COVID-19 vaccine by December. The head of the Presidential group was a 30-year R&D veteran of the large UK drug firm GSK, Moncef Slaoui. In 2017 Slaoui had resigned from GSK and joined the board of none other than Moderna. Under Slaoui’s Warp Speed, some $22 billion of US taxpayer money was thrown at different vaccine makers. Moderna was a prime recipient, a brazen conflict of interest but nobody seemed to care. Slaoui funneled some $2 billion in government funds to his old company, Moderna, to develop the mRNA covid vaccine. Only under public criticism did Slaoui sell his stock in Moderna, making millions in profit from Moderna’s role as a covid vaccine leading candidate. Shortly after resigning at the end of the Trump presidency, Slaoui was fired by his old firm GSK from a company subsidiary following charges of sexual harassment of a female employee.

In February 2020 Trump Secretary of Health and Human Services, Alex Azar, invoked the Public Readiness and Emergency Preparedness Act (PREP) to exempt Moderna, Pfizer, J&J and any future covid makers from any and all liability arising from damage or death caused by their vaccines for the Wuhan coronavirus. The legal protection lasts until 2024. If the vaccines are so good and safe, why is such a measure needed? Azar was former head of the US drug giant Eli Lilly. There are some serious questions that must be raised openly regarding the vaccine makers who are now pushing experimental highly controversial gene-edited formulations in human experiments.

F. William Engdahl is strategic risk consultant and lecturer, he holds a degree in politics from Princeton University.

July 30, 2021 Posted by | Corruption, Deception, Science and Pseudo-Science, Timeless or most popular | , , , , | 2 Comments

COVID-19: RDIF Points to Absence of Long-Term Studies on Vaccines Based on Monkey Adenoviral Vectors

By Aleksandra Serebriakova – Sputnik – 09.09.2020

The third round of trials for the AstraZeneca anti-COVID-19 drug is now on pause over “potentially unexplained illness” in a participant in the UK. On 11 August, Russia registered its own Sputnik V anti-coronavirus vaccine, which is said to have been developed in a different way.

The Russian Direct Investment Fund (RDIF) the investor which has funded the development of Russia’s Sputnik V anti-coronavirus vaccine, could not comment on the halt of AstraZeneca trials, it said in a statement.

However, RDIF pointed out that the fund’s CEO Kirill Dmitriev had previously discussed the differences between the human adenoviral vector-based platform used in Russia’s Sputnik V vaccine and those used by some of their international colleagues, that rely on “novel unproven technologies such as monkey adenoviral vectors or mRNA”.

“The safety of the human adenoviral vector used in Sputnik V has been proven over decades in over 250 clinical studies, as human adenovirus has been shown to be the safest vaccine delivery mechanism and the most ‘organic for humans’, as human adenovirus has coexisted with humans for over 100,000 years,” RFID said.

Meanwhile, “mRNA and monkey adenoviral vector-based platforms have not been studied over a long period of time,” RDIF CEO Dmitriev pointed out this Tuesday.

Commenting on the so-called “pledge of safety” earlier voiced by the CEOs of AstraZeneca, BioNTech, GlaxoSmithKline, Johnson & Johnson, Merck, Moderna, Novavax, Pfizer and Sanofi in relation to the development of the first COVID-19 vaccines, Dmitriev stressed that this plea was “insufficient” as it did not “discuss the lack of long-term studies on the carcinogenic effects and impact on fertility of newly-developed vaccine technologies”.

“Since some of the companies developing these vaccines have taken the ‘pledge of safety’, we would like to stress that public health and safety requires not only short-term evidence of a lack of serious adverse effects, but also the safety and efficacy proved by the results of long-term studies,” Dmitriev added.

AstraZeneca COVID-19 Vaccine Trials on Pause

It was revealed this week that the third round of trials for the AstraZeneca anti-COVID-19 vaccine has been halted due to a “potentially unexplained illness” which had developed in a participant in the United Kingdom, without further specifications about the nature of possible side effects. The vaccine in question was developed in partnership with Oxford University and has reportedly involved around 30,000 participants in the UK, US, Brazil and South Africa. AstraZeneca described the pause as “routine” so as to allow for a “standard review process” of “safety data”.

Russia’s First Anti-Coronavirus Vaccine

On 11 August, Russia registered the world’s first vaccine against COVID-19, called Sputnik V, which was developed by the Gamaleya National Research Centre of Epidemiology and Microbiology and the RDIF after several rounds of clinical trials. On Monday, the vaccine was made available to the public.

According to RDIF, Russia has now received requests for 1 billion doses of the vaccine; at least 20 countries, including the UAE, Saudi Arabia, Indonesia, Philippines, Mexico, Brazil and India, have expressed an interest in obtaining Sputnik V.

September 9, 2020 Posted by | Aletho News | , , , , , , , , , | Leave a comment