By MIDWESTERN DOCTOR – The Forgotten Side of Medicine

Ron Johnson has gradually become one of my favorite senators in American history. In 2020, he repeatedly advocated for early COVID-19 treatments to be made available to Americans (which had they been made available would have ended the pandemic).

Throughout 2021, he spoke out against the vaccine mandates and in November hosted a panel at the Senate which scrutinized the federal vaccine mandates and exposed how poorly those who experienced severe COVID-19 vaccine injuries were being treated. In January 2022, he hosted a panel which scrutinized the entire COVID-19 response, and in December of 2022, he hosted a panel focusing on everything we now know about the vaccines.

Being one of the most outspoken critics of the vaccination program in American history got him a lot of pushback, and in 2022, he decided to postpone his retirement to go through a grueling re-election campaign so there would be someone in the government who could advocate for everyone whose lives had been ruined by the COVID vaccines.

Despite being public enemy number one of the pharmaceutical industry, Johnson narrowly won, becoming the first politician in America’s history to run on the vaccine safety issue and win. Since then Johnson has kept his promise and fought for the vaccine injured (along with taking a variety of other difficult but important positions such as giving one of the most poignant speeches I’ve heard on the Ukraine War when he tried to block the Senate from continuing to fund it).

A lot of work has gone into producing each of the vaccine panels he’s hosted. On Monday, he hosted “Federal Health Agencies and the COVID Cartel: What Are They Hiding?” When it was all said and done, I believe this panel was the most effective presentation I have seen for explaining what happened throughout COVID-19 and waking people up to how much they have been lied to. Because of this I strongly encourage you to watch or share his presentation with people who you think might be open to understanding exactly what was done to all of us. This article will begin with his entire panel:

Lastly, for those who prefer to read, a transcript of Johnson’s symposium can be found here.

Note: for each of the videos embedded within this article, I (or the Vigilant Fox) edited them down to their most important parts. A lot of time was put into this article because of the importance of what was presented.

Federal Health Agencies and the COVID Cartel: What Are They Hiding?

Since the entire panel was 4 hours long, I recognize that many of you will not be able to watch all of it. For that reason, I tried to highlight what I felt were it’s most important parts.

First, in Johnson’s opening statement, he discusses just how hard it has been over the last three years to get any of the information his office is legally entitled to from the government. For example with (Fauci’s) NIH:

We are down to the last 50 pages [of the 4000 he originally requested]. They will not release these. It’s been now going close to 2 years. This is what has been provided to us. Do you think there might be some incriminating information in this?

Likewise, these agencies have completely brushed off all evidence something is wrong. For example, with the NIH:

Just like former NIH director Francis Collins Collins told me when I asked about all the deaths being reported on VAERS, [he said], “Senator, people die.” The fact that both of these statements are as true as they are callous highlights the challenge we face in exposing the truth.

While with the FDA:

I’ve written 4 [letters on hot-lots] starting in December of 2021. The first letter compared 25,000 lots of COVID vaccine to 22,000 lots of flu vaccine. One COVID lot had 5,297 adverse reactions associated with it. The worst flu lot had a 137. So 5,300 versus 137.

365 COVID lots had more than 100 adverse events. Only 10 flu lots had more than 100. And 80% of the serious adverse events, those with emergency room visits, hospitalization, or death were associated with only 5% of the lots. So, again, to me, I’m from manufacturing. That shows to me a manufacturing process out of control.

[It] took us a year to get some kind of response and, basically, response from the agencies was, “we don’t see any variation in lots.”

Johnson then illustrates how the current political climate has undermined everything science once stood for:

“Vaccine injuries are rare.” “The benefits outweigh the risk and that the science is clear and overwhelming.” “And anyone challenging this narrative is an is an anti science conspiracy theorist.” In other words, second opinions are not allowed. To me, this attitude is the antithesis of science.

I am amazed at the knowledge mankind has obtained over the millennia. But I would argue that what we don’t know vastly exceeds what we do know. So as we pursue truth, we must pursue it with the humility that that reality demands.

Johnson’s opening statement was then followed by Robert Malone:

I’ll be succinct. The SARS CoV 2 modified mRNA based vaccine products were deployed via emergency use authorization without adequate nonclinical and clinical testing and without full disclosure of known patient risk and efficacy data. This violated well established legislatively mandated patient informed consent requirements. The FDA and HHS justified these actions as necessary due to reliance on deeply flawed modeling data indicating that SARS CoV 2 was associated with an infection fatality rate of 3.4%.

Note: the IFR was subsequently shown to average between 0.018%-0.03% for everyone under 60 and was approximately 0.506% for those between 60-69 years of age.

Subsequent clinical research experience has revealed a number of problems with the genetic vaccine technology based SARS COV 2 products, which have been marketed as vaccines. In most cases, there has been an effort to obscure or deny facts in public communication by government and pharmaceutical industry representatives.

Malone then listed the key issues with the vaccines, to which Johnson replied:

Doctor Malone, I think one of the things that always bothers me is [that] so much of what we’re learning in terms of harms of these vaccine was clearly known before they were rolled out.

Jessica Rose spoke next. After concisely summarizing all of the issues that had been found within VAERS, she concluded with:

Standard operating procedures for analysis of safety signals emergent from VAERS when utilized reveal causal links between the COVID 19 injectable products and the adverse events investigated. Standard operating procedures are not being followed by the owners of the data, namely CDC, HHS, and FDA, and this equates to hiding the millions of people reporting not only adverse events but injuries in the context of the COVID 19 injectable products.

Note: Rose also reviews the science behind why vaccinated individuals keep on catching COVID-19.

Edward Dowd then concisely presented the years of work his team has done to quantify just how devastating the vaccines have been for the world.

To quote part of Dowd’s testimony:

When analyzing the excess death human cost…in 2020, there were approximately 458,000 excess deaths, of which 73% were aged 65 and older and 15 to 64 comprising just 27%. However, in 2021, with the rollout of the “safe and effective vaccine,” there were approximately another 500,000 excess deaths, but a mix shift had occurred from older to younger. In 2021, the 65 plus age category was [only] 57…while the 15 to 64 cohort increased to 43%.

The absolute excess death increase from 2020 to 2021 for the productive working age 15 to 64 was 73% [124,000 to 215,000].

The total excess death since the rollout of the vaccine in the US, including 21, 22, and 23 is approximately 1,100,000. We estimate the economic cost, productive working age people dying at $15,600,000,000 When analyzing disabilities, it’s interesting to note that there were no excess disabilities in 2020.

Using the civilian labor force, we have calculated an increase of 2,300,000 individuals with disabilities costing the economy an estimated $77,000,000,000. When analyzing lost work time, which we call injuries, we estimate 28,400,000 individuals are chronically absent resulting in an estimated economic cost of a $135,000,000,000 since 2021…Obviously, the policy cure was undeniably worse than the illness.

Kevin McKernan then discussed his groundbreaking discovery that there was widespread DNA plasmid contamination of the COVID vaccines and how horrendously the drug regulators have responded to that discovery.

This work has been replicated by many labs around the world, and now the FDA, the EMA, and even Health Canada, have admitted to this. The regulatory agents have admitted that Pfizer also omitted the SV40 sequences that are in their vaccine. They’ve deemed this contamination to be of little consequence, claiming the DNA is of too little concentration to matter or to be containing DNA of no functional consequence. These statements are false and are not supported by any independent testing by these regulators.

After the regulators have admitted to being deceived, they asked the opinion of the party that deceived them how bad was the deception. They shockingly believe the answer they were given, which is that these sequences have no relevance to plasmid manufacturing. As someone who has worked on the Human Genome Project manufacturing millions of plasmids, I can assure you that this is an overt lie. DNA contamination can lead to insertional mutagenesis. This is actually declared in Moderna’s own patent regarding the mRNA vaccines.

This is also supported by Lim et al, which speaks to the rate of spontaneous integration in the genome during transfection. We are using transfection after all with LMPs. The SV40 DNA is in fact functional. It is published as a potent gene therapy tool in a nuclear targeting sequence as described by David Dean et al.

The SV40 promoter DNA is also known to bind to the tumor suppressor gene known as p53.

Note: p53 defects are commonly linked to cancers.

We’ve applied these vaccine system cancer cell lines and have evidence that it enters the cell and can survive several cell divisions. We have preliminary evidence, although this requires replication in other labs, that this DNA can integrate into the genome. We found 2 spike sequence integration events in ovarian cancer cell lines of CAR 3 into chromosome 12 and 19 very recently. Since these vaccines were expected to only contain mRNA, they were never assessed for genotoxicity studies. These studies were therefore being conducted as guinea pig US citizens as we witnessed an unprecedented rise in cancer drug sales since the vaccines rolled out.

It is time for our representatives to repeal or review the PDUFA Act of 1992.  This act allows regulators to defray the cost of regulation by accepting payments directly from the companies they regulate. Over half of the FDA’s budget is sourced through this act.

Note: I discussed the significance of the vaccine plasmid contamination in more detail here.

Dr. David Gortler (who previously served as a senior advisor at the FDA) then explains why the contamination and widespread variability we are seeing in the vaccines (e.g., the hot lots) being completely ignored is so unprecedented:

Federal rules requiring ingredient transparency date all the way back, believe it or not, to 1862 [and] it’s the whole reason the FDA was started in 1906. Prior to COVIDsRNA injections, the FDA had approved 4 different RNA based products. Onpattro, shown here, was the 1st RNA product approved back in 2018…as you can see by looking at this label, Onpattro prominently details the exact structure, milligram strength, and molecular weight. Highlighted in green at the very top, you’ll see it specifies [what its] lipid nanoparticles are engineered for.

In contrast to the previous labels I’ve shown, here is the official FDA label for COVID RNA injections. As you can see just looking at it, it details a lot less information. We don’t [even] have the structure.

Of note, in pharmacology, even very minor deviations in any molecular structure can mean the difference between a drug and a poison…The lack of transparency means that scientists can’t use modeling to test lipid nanoparticles for safety receptor specificity or analyze inequality [in batches of those products].

Unfortunately, around 70% of the 127 page document that explains the methodology to perform quality control on RNA injections are redacted much like the document I’ve shown here.

Next Dr. Harvey Risch discusses the “crushingly obsessive push to COVID vaccinate every living person on the planet” and provides a concise overview of the horrific bioweapons industry which gave birth to COVID-19 and then tried to pivot to vaccinating everyone rather than accept responsibility for what it had done.

Next, Barbara Loe Fisher, an activist who has spent decades fighting for vaccine safety shared the broader context of what we are now dealing with.

I worked with parents in congress to secure safety and informed consent provisions in the National Childhood Vaccine Injury Act of 1986. It was an historic law, the first official acknowledgment by government that federally licensed and state mandated vaccines can and do injure and kill some children. In January, my eyewitness perspective of how and why child vaccine victims and their parents were betrayed after that law was passed 38 years ago, was featured in a 2 hour conversation I had on the Highwire.

I encourage everyone to watch it and learn how parents trusted that the 5 years of work we put into that 1986 act to successfully secure life saving, informing, recording, reporting, and research provisions in it, and to protect the legal right of vaccine victims to sue vaccine manufacturers for product design defects, and to sue negligent doctors for medical malpractice, and to create an expedited, more just, less traumatic federal vaccine injury compensation system alternative to a lawsuit were all destroyed by congressional amendments, by federal health agencies, and the US Supreme Court after that law was passed. Following that betrayal of trust, Congress directed federal agencies to create lucrative public private business partnerships with the pharmaceutical industry, a business deal that has broken America’s public health system.

Note: I previously wrote about how the 1986 Vaccine Injury Act forced the government to create VAERS (as parents had no way to report vaccine injuries) and ever since that time, the government has done everything it could to undermine VAERS.

Johnson then shares a poignant observation with Fisher that illustrates how effectively the pharmaceutical industry has bought out our media:

By the way,I became aware of you from that excellent documentary which I would also recommend. What struck me about [it] is back then in 1982 through 1986, you could talk about these things. You could advocate for your child who’s vaccine injured.  You weren’t ostracized. You were actually welcomed here in the senate by people like Senator Hatch and Senator Kennedy and you got this [law] signed by Ronald Reagan.

To which Fisher replies:

I never imagined when I began this work in 1982 that the day would come when I would not be able to exercise freedom of thought and conscience in the country I love. And I thank you for allowing me to exercise that right today.

Next, Bryan Hooker, the parent of a severely vaccine injured adult son shares his 23 years of work (e.g., 15 peer-reviewed papers) to get the data on vaccine injury the CDC has been hiding for decades.