SENATOR JOHNSON’S ENQUIRY: THE CORRUPTION IN THE CDC, FDA AND BIDEN ERA EXPOSED

And now onto our main discussion regarding the… and many of us would be familiar with Senator Ron Johnson, especially following his work in unravelling the covid debacle in the US. Interestingly, in light of the work he had done, Senator Ron Johnson had planned to retire in 2022 but ran for re-election specifically to help those affected by the vaccine. But, one of the things that’s been the most striking about Ron Johnson’s attempts to stop the COVID vaccines has been the revelation of just how little legislated power a Senator has to compel the CDC or FDA to do the right thing (for example, many of the key COVID government documents that Senator Ron Johnson’s office uncovered were never provided by the H.H.S. in the Biden-Harris administration).

Nonetheless, Senator Ron Johnson has been extremely methodical and patient in seeking a way to change the current paradigm. He has now ascended to a very unique position: being chairman of the Senate Permanent Subcommittee on Investigations. This committee has long been one of the most powerful and broadest investigative bodies in Congress. In parallel, since the second Trump administration has a far more fundamentalist approach to healthcare through the MAHA agenda, rather than stonewall Johnson, this administration has ensured that the documents he is requesting are now being released. And because of this, he was recently able to hold a pivotal Senate enquiry that conclusively showed the Biden Administration, FDA, and CDC were aware the COVID vaccines were causing heart attacks but continually hid that from the public to keep pushing the COVID vaccines on the public.

In this Senate enquiry led by Senator Ron Johnson, cardiologist Dr. Peter McCullough delivered a stark warning about the risks of vaccine-related myocarditis, a crisis downplayed by federal health officials. Testifying before the Senate Homeland Security Committee, Dr. McCullough, with over 1,000 publications, revealed data on heart damage linked to mRNA COVID-19 vaccines, particularly in young men, and criticized oversight by agencies like the FDA and CDC.

Dr. McCullough condemned mandates imposed on athletes by sports teams, with no safety provisions, stating that “Ninety percent of vaccine myocarditis cases involve young men, and ninety percent require hospitalization.” In addition, subclinical myocarditis, where patients experience heart palpitations, blood pressure swings, and atypical chest pain, is also concerning, with symptoms persisting post-vaccination. A recent Journal of the American College of Cardiology report confirmed cardiac arrests years after vaccination, with vaccine micro-scars found in the heart. ANd so, Dr McCullough’s testimony exposed a wave of vaccine-related deaths, with subclinical myocarditis setting the stage for fatal arrhythmias months or years later. Kindly watch this excerpt.

Now, a significant reason that legislators in the Biden-Harris administration and the FDA were able to get away with concealing or downplaying critical information is that those who raised concerns were silenced. And here, this is not even about the political weaponisation of institutions or even the creation of the censorship industrial complex (which are issues that emerged in the COVID period) – RATHER, this is about the fact that those who were vaccine injured who went to Senate Hearings to report of their experiences and provide empirical evidence were gas lit and shut down.

And herein lies one of the most critical issues that contributed to erosion of the integrity of the medical system in the US (and others parts of the world). It is that: not only were government officials working with incorrect information and WHO dictates about the COVID virus and vaccines, and not only were covid responses highly politicised and divorced of scientific integrity, BUT even when people sought to highlight urgent concerns that would have improved the government’s response, governments often failed to fulfil their duty of care by listening.

Well, another concealed and previous denied development that was highlighted in the hearing pertains to the notorious white fibrous blood clots from the COVID vaccines. These clots are stretching over 20 inches long in a significant number of bodies where they were examined, and a number of doctors reported seeing them after the rollout of COVID jabs – in both patients they were seeing and post-mortem bodies. For instance, During his 40-year career as a pathologist, Dr. Arne Burkhardt had never observed this type of unusual blood clot until after the rollout of the C19 injections. This type of clot was found in several living vaccinated patients, including a 40 year-old former marathon runner.

THE LACK OF ADEQUATE REGULATION AND ACCOUNTABILITY IN THE MEDICAL INDUSTRY

This then necessitates that we focus our attention on the regulatory body that was supposed to ensure that this problem does not occur to begin with, being the FDA. Not only because they are a regulatory body but because products approved by the FDA have a broad scope of impact, given how they are imported around the world. And so, first let’s have a recapitulation of the FDA;s history. And this history, even in its abridged version, demonstrates that in the absence of a regulatory body, corporations have a tendency to place harmful products on the market that they present as having a plausible impact on people’s health.

So the FDA is conceptually necessary to prevent the continuation of the harmful business food and drug manufacturing process observes in the US and also around the world, like Coca-Cola using cocaine in its drink and presenting it as a fatigue relieving medication, or companies including spices and preservatives in food to mask the taste of expired food. So, why has a body that has a valid and plausible reason for existence been complicit or culpable in some of the issues in the medical industry?

THE INHERENT PROBLEMS IN THE FDA’S DRUG APPROVAL PROCESSES

Let’s start with the drug approval process. And here it is important to note that the FDA’s approval process may favour drug companies over consumers — and FDA-approval does not guarantee safety. In fact, Big Pharma actually pays for the majority of drug safety reviews, provides the FDA with safety data for the review and has the option to have drugs approved faster with fewer clinical trials. In addition, FDA approval is based on evidence — provided by the company that makes the medical product — that the benefits of the product outweigh the risks for most patients for a specific use. It doesn’t necessarily mean the product is safe.

Furthermore, a new drug takes several steps before it makes its way into a consumer’s medicine cabinet. Unlike medical devices that are cleared for sale without extensive testing if a similar device is already on the market, drugs must go through clinical trials before they are available to consumers.

Now, while the process of approving a new drug may seem thorough on paper, critics say it assumes the world is a perfectly controlled environment. Also, clinical trials have short timeframes and can’t thoroughly determine safety. Michael A. Carome, who is the Public Citizen’s Health Research Group director further stated on this very subject that “When a new drug is first approved by the FDA, it typically has only been tested in several hundred to a few thousands patients in carefully controlled clinical trials that last several weeks to several months and that exclude many types of patients who will end up being prescribed the drug, As a result, only the most common types of serious adverse events will be detected prior to FDA approval.” In fact, the FDA calls drug approval a “balancing act” between acceptable risks and benefits on its website.

THE FDA HAS A CONCERNING HISTORY EVEN IN TRACKING OR RESPONDING TO COMPLAINTS ABOUT DRUGS AND PRODUCTS

Now, multiple experts expressed concerns about the risk of the vaccine causing premature births, a risk found in a similar product made by GlaxoSmithKline that prompted thecompany to halt testing in 2022. In Pfizer’s trial, there were more premature deliveries in the vaccinated arm than the placebo arm—5.7 percent in the former versus 4.7 percent in the latter. Dr Paul Offit, who is one of the FDA’s advisers, said that this is an issue hanging over the program. But take a guess at how the FDA responded; simply, the FDA declined to comment on the issue during, though staffers wrote in a brief that there was “potential uncertainty” regarding premature births. But, this is not the first instance where FDA leadership was caught unprepared to deal with complaints about products, because medical device dangers were hidden in FDA reports for DECADES.

A major consideration in this discussion is not just Pfizer’s approach to vaccine safety – as indicated at the beginning of our discussion, it is the very essence of the medical industry and the fact that – despite the constructive role it is supposed to play in society, it is one of the least effectively regulated industries in the world, and corporations and global organisations take advantage of this. For instance, the COVID VACCINE FORMULA was SWAPPED IN a SINISTER FDA FRAUD! Justin Leslie, who was armed with damning videos and documents, revealed Pfizer pulled a fast one on the FDA. In essence, what occurred is that after clinical trials, Pfizer swapped the vaccine’s phosphate buffer saline (or PBS) for a tris buffer system. Why? Well, because the PBS needed -80°C storage, but the tris allowed easier distribution. The problem is, ALL trial data was based on the PBS formula—NOT the tris one injected into kids!

Unfortunately, it does not end here. What has always been of concern to me and no doubt to many of you as our viewers is the utter lack of effective regulation measures for medical devices by the FDA as well – so much so, that the regulation measures that are supposed to ensure that the devices are safe to implant or that any issues are reported and responded to swiftly are much worse in comparison to the measures the FDA uses for prescription drugs.

This lack of accountability has also manifested with medical practitioners themselves. More specifically, there were a number of cases reported in the world where doctors would falsely prescribe chemotherapy to patients who did not have cancer. In one case, 5 years ago, a Michigan office manager risked his career to expose a doctor who gave chemotherapy to patients who did not have cancer.

Written by Lindokuhle Mabaso