Please don’t miss. Ron Johnson was slow out of the blocks, but...

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    Please don’t miss. Ron Johnson was slow out of the blocks, but he’s become a solid Covid voice. The only one in DC.

    “..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.”

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

    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.[..]

    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.


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