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If It’s Okay for Mice, It’s Good Enough for People, Right?

By Madhava Setty, M.D. | The Defender | August 26, 2022

Its audacity on full display, Pfizer — arguably the most criminal corporation in history — has asked the U.S. Food and Drug Administration (FDA) to greenlight its new bivalent COVID-19 vaccine that targets the Omicron BA.4 and BA.5 subvariants for people 12 and older “to help the country prepare for potential fall and winter surges of the coronavirus,” Pfizer CEO Albert Bourla said in a statement.

Bourla’s good intentions are sadly thwarted by FDA regulations that require an Investigational New Drug (IND) application be submitted and approved before a drug can be tested in humans.

Luckily, the FDA can circumvent the inconvenience of its own regulatory processes by allowing itself the ability “to authorize use of an experimental drug in an emergency situation that does not allow time for submission of an IND in accordance with 21CFR, Sec. 312.23 or Sec. 312.20.”

Section 312.20 of the Code of Federal Regulations specifies that a clinical investigation cannot commence until an IND application has been submitted and approved. Nevertheless, Pfizer on Monday submitted an IND for its new formulation.

Now that the FDA and Pfizer have crossed their Ts and dotted their Is to make sure all the rules are followed, how do we know these products are safe and will work?

This is where the rodents come in — the products seem to work on mice.

As NPR reported, “For the first time, the FDA is planning to base its decision about whether to authorize new boosters on studies involving mice instead of humans.”

Yes, it’s an unprecedented move by the FDA, but Dr. Ofer Levy, professor of pediatrics at Harvard and advisor to the FDA argues that the country has had enough experience with the vaccines at this point to be confident the shots are safe and that there’s not enough time to wait for data from human studies.

He has a point. There were still only 30,479 uninvestigated deaths reported in VAERS after administration of the shots as of Aug. 19.

In any case, why should the FDA be concerned with such things as human studies in the first place?

This maneuver by the FDA may finally unshackle the agency from its overly restrictive responsibility to fulfill its own mission and become more agile in bringing products to market.

Not to be left behind, Moderna also requested the FDA authorize its bivalent vaccine for human beings over the age of 17.

Similar to the Pfizer vaccine, Moderna’s vaccine also, for good measure, will encode for the spike protein for the original ancestral SARS-CoV-2 strain, which for all intents and purposes, does not exist on our planet any longer.

Meryl Nass, M.D., summarized it this way:

“No clinical trials. (You need to obtain an IND before you can start testing the vaccine in humans. Pfizer applied 4 days ago.)”

Taking no chances, the FDA will not convene the Vaccines and Related Biological Products Advisory Committee (just like the first time the FDA authorized boosters) and has announced this today to see how much opposition the agency gets.

Can we dispense with the pretense any of this is about health?

No sane person vaccinates the entire country with an experimental vaccine without trials — particularly since the whole country already has some immunity, the virulence is low and the evidence supports higher all-cause mortality with an increasing number of vaccine doses.

What is in the vaccine that they are desperate to inject us with?

Madhava Setty, M.D. is senior science editor for The Defender.

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

August 27, 2022 Posted by | Deception, Science and Pseudo-Science | , , , | Leave a comment

Silenced healthcare workers speak out publicly for the first time

By Steve Kirsch | August 27, 2022

I created a form to ask healthcare workers to speak anonymously about what they are seeing.

Here’s what they said in their own words.

Here is a quick summary of some of the things they said:

  1. They are afraid to come out publicly due to intimidation tactics such as loss of job and/or license to practice medicine.
  2. Unvaccinated healthcare workers are extremely upset with the medical community. They feel they have been treated unfairly.
  3. It is the vaccinated workers who are getting sick with COVID, but it is the unvaccinated who are punished with constant testing, restrictions, and threats of losing their jobs.
  4. The COVID shots are a disaster. Even for the elderly which is supposed to be the most compelling use case, death rates in elderly homes went up by a factor of 5 after the shots rolled out. Each time the shots are given, the deaths spike. Nobody is talking publicly about this. It’s not allowed.
  5. “I have a patient who owns an adult care home that gave vaccinations to their six adult clients. They all died within a week.”
  6. Doctors are seeing rates of injury and death increase dramatically in all ages of people. The injuries are only happening to the vaccinated. There is no doubt that this is happening but many doctors have so much cognitive dissonance that they don’t see it.
  7. One nurse with 23 years of experience says she’s never heard of anyone under 20 dying from cardiac issues until the vaccines rolled out. Now she knows of around 30 deaths.
  8. “I have been a nurse for 36 years. I have NEVER witnessed people in their 20s and 30s having strokes, atrial fibrillation, or cardiomyopathies until the Covid vaccines. I work in cardiology. When I mention that someone should look at the vaccines as a possible reason, I am immediately silenced and told, “It is NOT from the vaccine.””
  9. Doctors aren’t recording vaccination status in the medical records so that all the deaths are attributed to the unvaccinated.
  10. Doctors are deliberately ignoring the possibility that the vaccines could be the cause of all the elevated events. The events are simply all unexplained.
  11. Many doctors have either quit or will quit.
  12. Some doctors and nurses at top institutions such as Mass General Hospital have falsified vaccine cards. They publicly toe the line and encourage their patients to take the shot knowing full well it is deadly. They value their job more than the lives of their patients. The important thing is they are risking 10 years in jail for doing this. These highly respected medical workers are telling the world that these COVID shots are so dangerous that they are willing to risk 10 years in prison to avoid taking the shot. That’s the message America needs to hear. And if Biden were an honest President, he would call for full amnesty and protection from retaliation for all these cases if people admitted publicly they did this. He’d be amazed at the number of responses he’d get. But he won’t do that because it would be too embarrassing for his administration.
  13. Things don’t seem to be getting any better.
  14. The medical examiners all over the world are not doing the proper tests during an autopsy to detect a vaccine-related death. Without doing the necessary tests, it is very hard to make an association. There isn’t a single “guidance” document from any medical authority anywhere in the world to do these tests on people who die within 3 months of their last COVID vaccination. This is why no associations are found: they aren’t looking and it is deliberate. The mainstream press doesn’t call them out on this either.
  15. Doctors are being forced to take other vaccines so the hospital can meet their quota. This was admitted to them.

The document paints a very troubling picture of healthcare in America

It is very difficult to read that document and come away thinking that everything is working fine.

If you read the document and think everything is just fine, it means one or more of the following is true:

  1. You work in the White House
  2. You work at the CDC, FDA, or NIH
  3. You are a member of Congress or are a staff member for a member of Congress (Ron Johnson and his staff are excluded)
  4. You work in the mainstream media
  5. You are a top executive at a mainstream social media company
  6. You work in the mainstream medical community (doctor or academic)
  7. You are a miserable excuse for a human being
  8. You are an exemplary blue-pilled individual; you are just the type of citizen that your government wants to have

If you are troubled by what you read, here is what you can do

If you read through the document and are troubled by what is going on and you want to hold these people accountable, there are two simple thing you can do to make a difference:

  1. Share this article on all your social media platforms
  2. Make a donation to help re-elect Senator Ron Johnson (click here for the donation link). He’s the most important person in Congress that will hold these people accountable. This is why he’s the #1 target of Democrats.

Want to speak to any of these people?

If you are a member of the press and want to speak to any of these people, you can use the Contact me form to make your request. In the Notes part of the form, specify the database line number of the person(s) you want to contact.

Please share this post widely. Do it now.

The mainstream press will not share this information. This isn’t misinformation; these are all true stories, many of which are impossible to explain if the vaccines are truly safe and effective. Taken together, they are a stunning indictment of a medical system that has been corrupted through government incentives.

It is important for people throughout the world to hear from the healthcare workers whose voices have been silenced by the medical community. Please do it now.

August 27, 2022 Posted by | Science and Pseudo-Science, Timeless or most popular | , | Leave a comment

Norwegian Schools Are Disseminating Government-Approved Covid Misinformation

BY KATHRINE JEBSEN MOORE | THE DAILY SCEPTIC | AUGUST 26, 2022

Who needs conspiracy theorists when you’ve got school books teaching children that Covid vaccines are “95% effective”?

This autumn, a new school book was introduced for the ninth grade in Norway. Fabel 10 was revised in 2021/22, but has only now been introduced in schools across Norway. Not only does the book overstate the effectiveness of the novel mRNA vaccines, it decries anyone questioning that as conspiracy theorists.

One excerpt reads:

Since the Covid pandemic broke loose, Covid deniers and vaccine sceptics have spread disinformation about coronavirus through social media. They claimed among other things that COVID-19 was no more deadly than the flu, that the vaccine was dangerous, and that restrictions were unnecessary. On Saturday March 20th 2021, 200 Covid deniers gathered in front of the Parliament. They burnt face masks to show that they thought they were unnecessary.

This short paragraph is easily debunked. Readers of the Daily Sceptic know that Covid now has an infection fatality rate about the same as influenza. We also know that side effects from the Covid vaccines – both the mRNA and the viral vector vaccines such as AstraZeneca’s – are more common than for other tried and tested vaccines. Remember when the Pandemrix vaccine rollout was halted because of a link to rare instances of narcolepsy? Multiple studies show Pfizer and Moderna’s Covid vaccines increase the risk of myocarditis and pericarditis in especially younger males – the demographic who make up precisely half the readership of Fabel 10. The German Government even admits that as many as one in 300 doses of the mRNA jabs produce serious injury. Compared to the danger that Covid poses to most people, does that make vaccines worth having?

And as for restrictions, a new consensus is gaining momentum. Whereas back in 2021, when the book was written, it was mainly agreed that lockdowns and other Covid restrictions were necessary to halt the spread, and countries with low Covid fatalities would credit these non-pharmaceutical interventions for their comparatively low excess mortality, studies later proved them incorrect. Lockdowns and excess mortality were not correlated. Whereas back in the early days of the pandemic, only a few, brave voices spoke up about their concerns, now even Rishi Sunak, who helped implement Britain’s lockdowns, admit they were detrimental to overall health and the economy and did little to stop infection. Yet in Norway, pupils are stuck in the reality curated more than a year ago, a reality that has now been revealed to most as bonkers.

And those 200 “Covid deniers” who burnt face masks deserve praise for being a tiny minority speaking up for science at a time where “the science” became an allegory for anything the authorities wanted us to do without having to prove why.

The book also states that vaccines are “95% effective against COVID-19 infections”. This is clearly nonsense, and doesn’t need further debunking. We all know of multiple-jabbed people getting infected several times over, and that infection rates in highly vaccinated countries went through the roof after the vaccine rollout.

Perhaps the book will serve as a test to pupils old enough to gather information from multiple sources. Some might agree with what they’re presented with, while others will see through this Government-approved misinformation. But that’s not really the sort of education you want in a free, democratic country. The book doesn’t invite 14-15 year-olds to question or discuss – it presents them with all the (wrong) answers. That’s bad enough in itself, but what’s worse is it tells them to ridicule those who don’t agree. The chapter on Covid and conspiracy theories could have been a great opportunity to teach children about academic freedom, online censorship, tolerance, debate, dissent and freedom of speech. Instead, it serves straight-up, Orwellian newspeak to young minds in a way the CCP would be proud of.

August 27, 2022 Posted by | Civil Liberties, Science and Pseudo-Science | , , , | Leave a comment

As COVID Vaccine Injuries Pile Up, It’s Worth Remembering: Medicine Is a Leading Cause of Death in the U.S.

The Defender | August 24, 2022

In his 1974 book and accompanying article with the shared title of “Medical Nemesis,” philosopher and theologian Ivan Illich boldly asserted that medical professional practice and related health policies, which he characterized as “both industry and religion,” had become “a major threat to health.”

Leading medical figures such as Richard Smith, a long-time medical journal editor and critic of fraudulent health research, later credited Illich with “remarkable” prescience about iatrogenesis — the cover term for ailments “where doctors, drugs, diagnostics, hospitals, and other medical institutions act as … ‘sickening agents.’”

Already by 1999, the Institute of Medicine had flagged medical error as being in “the top ranks of urgent, widespread public problems.”

Then in 2000, Johns Hopkins public health expert Dr. Barbara Starfield got more specific, fingering iatrogenesis as America’s third leading cause of death.

The United States leads the world in per capita pharmaceutical spending, which may explain why the worldwide ranking of iatrogenesis as a cause of death, while still alarming, is slightly lower — fifth, rather than third.

In her landmark paper in the Journal of the American Medical Association, Starfield estimated around 225,000 American deaths annually — or possibly as many as 284,000 — from causes such as unnecessary surgery, contraindicated care, medication errors and drug adverse effects.

Writer Jon Rappoport — who interviewed Starfield in 2009, and regularly reminds readers about her “stunning” findings on medically caused death in America — observed in 2015, that while there was “every reason for [Starfield’s paper] to cause a firestorm in the press, and in the halls of government … that’s not what happened.”

Instead, “intentional amnesia set in” — until 2016.

That year, two more Johns-Hopkins-based authors, Dr. Martin Makary and Michael Daniel, briefly revived the topic in The BMJ (formerly the British Medical Journal ), again citing “lethal events” resulting from medical error as “the third biggest cause of death in the US,” and appraising their figure of roughly 251,000 annual deaths — nearly 1 in 10 overall deaths — as a conservative underestimate.

A less noticed 2013 article in the Journal of Patient Safety judged the practice of medicine to be causing on the order of 440,000 American deaths each year, with those authors calling for an end to the “Wall of Silence” surrounding such unfortunate occurrences.

Makary, who is not shy about pronouncing 20% of all medical procedures unnecessary, told The Washington Post in 2016, “It boils down to people dying from the care that they receive rather than the disease for which they are seeking care.”

Both Starfield and Makary also strenuously objected to victim-blaming, explaining, “It’s the system more than the individuals that is to blame.”

Although the BMJ article forced WaPo and other mainstream media outlets to briefly pronounce death by medicine a “hot topic,” the problem was quickly “disappeared” from view again, with Makary, a couple of years later, lamenting the lack of any meaningful health system correctives.

Tip of the iceberg? Bad outcomes often go underreported

Everyone who has tried to estimate the harms caused by modern medicine has called attention to the difficulty of truly getting a handle on the phenomenon due to underreporting and limitations of existing datasets, which likely reveal only the “tip of [the] iceberg.”

The first limitation is that most data used to calculate medicine as a leading cause of death come from hospitalized patients.

However, according to another 2000 study cited by Starfield, drug-related adverse effects are also high in outpatient settings, affecting somewhere between 4% and 18% of such patients.

In fact, researchers of that era estimated outpatient snafus resulted in nearly 200,000 additional deaths annually.

A second and related data shortcoming is that the focus on mortality tends to obscure non-fatal outcomes such as disability and, using Starfield’s word, “discomfort.”

In the late 1990s, researchers reported that medicine gone awry was leading to millions of additional physician visits, prescriptions, emergency department visits, hospitalizations and long-term admissions as well as billions in extra costs.

By 2018, a medical expert estimated the number of “severe patient injuries resulting from medical error” to be “40 times the death rate.”

A third problem is that when the Centers for Disease Control and Prevention (CDC) compiles its annual list of the most common causes of death, it does so using death certificate data and the International Classification of Disease (ICD) codes listed on the death certificates.

But as Starfield concluded, “How cause of death and outpatient diagnoses are coded does not facilitate an understanding of the extent to which iatrogenic causes of ill health are operative.”

Makary noted that the CDC does not require reporting of fatal medical errors, meaning that “causes of death not associated with an ICD code, such as human and system factors, are not captured.”

Those factors, Makary said, encompass “inadequately skilled staff, error in judgment or care, a system defect or a preventable adverse effect,” and problems such as “computer breakdowns, mix-ups with the doses or types of medications … and surgical complications that go undiagnosed.”

As one example, a family whose young child died after being given an overdose of sodium chloride solution learned that many states have “absolutely no requirements, or proof of competency” for the pharmacy technicians who compound hospital IV medications.

A fourth challenge involves difficulties of definition and classification. For example, are medical mistakes errors of omission, execution or planning?

What about adverse drug reactions that are dose-dependent? Are reactions predictable (that is, based on known facts about toxicity, side effects and drug interactions) or unpredictable (e.g., arising from factors such as allergy, intolerance or “idiosyncrasy”)?

In addition to drug mess-ups (such as incorrect administration, poisoning or therapeutic failure), iatrogenic effects can ensue through other avenues — from diagnostic procedures (both mechanical and radiological), surgery and other invasive procedures, hospitalization, unsafe injection practices, unsafe blood transfusions or the “treating doctor himself/herself.”

For example, studies highlight significant risks from screening colonoscopy — including perforation, infection and hemorrhage — with perhaps as many as 4% of recipients experiencing complications serious enough to send them to the hospital within a month of the procedure.

Cause-of-death rankings in COVID era

Makary noted the taboo nature of iatrogenesis, stating “We all know how common [medical error] is” and “We also know how infrequently it’s openly discussed.”

The CDC, meanwhile, is frank about the fact that ranking causes of death “is, to some extent, an arbitrary procedure” that flows from its in-house decisions about which causes are “eligible to be ranked.”

It also admits its rankings “do not necessarily denote the causes of death of greatest public health importance.”

With the advent of COVID-19-related medical measures and health policies, there is an urgent need to shatter the taboo and shine more of a spotlight on the public-health-important medical killing machine.

For example, did the dramatic two-year decline in life expectancy reported for 2020, and the three-year decline in the last-place state of New York — vaguely blamed on the “pandemic” and drug overdoses — have something to do with the imposition of perverse, government-incentivized COVID-19 treatment protocols emphasizing frequently fatal drugs like remdesivir?

Does the skyrocketing all-cause mortality observed since 2021 have anything to do with the U.S. Food and Drug Administration’s enabling of deadly COVID-19 vaccines, in all likelihood fraudulently authorized?

With what is known and what we continue to learn about COVID-19 vaccine dangers, the CDC’s current disease rankings —  which list heart disease, cancer, COVID-19, accidents and stroke as the five leading causes of death — demand close scrutiny.

Although multiple risk factors are certainly at play for the five causes of death, the COVID-19 jabs are indubitably adding to the death and disability rolls in those areas, with:

  • Widespread reports of fatal and disabling heart problems following vaccination.
  • Pathologist accounts of increased incidence of unusually large and aggressive “turbo” cancers, especially in younger patients.
  • Data from around the world showing the vaccinated to be at higher risk of dying from COVID-19.
  • Motor vehicle accidents surging in tandem with the rollout of COVID-19 vaccines — with news accounts linking the crashes to known adverse events such as seizures and mysterious “medical episodes.”
  • Published studies describing various types of stroke in the aftermath of COVID-19 vaccination.

Research has linked kidney disorders, also on the CDC’s list of “top 10” causes of death, to both remdesivir and the COVID-19 shots.

In two Zogby polls commissioned by Children’s Health Defense, 15%-22% of respondents who had received a COVID-19 vaccine reported being diagnosed with a new medical condition “within a matter of weeks to several months.”

In the first poll, the top five conditions listed by respondents were blood clots, heart attack, liver damage, leg or lung clots and stroke.

In the second poll, the top conditions included the same, plus autoimmune conditions, disrupted menstrual cycles, Guillain-Barré syndrome and Bell’s palsy.

From 26%-30% reported knowing someone else who also had received a medical diagnosis after taking a COVID-19 vaccine.

Not an error

At this juncture, with damage from the killing protocols and fraudulent jabs on growing display, it is no longer possible to hide iatrogenesis behind the innocent-sounding term “medical error,” for it is increasingly clear that we are also talking about intentional harm and even genocide.

For Illich, the remedy for this “sinister” and “health-denying” medical civilization involved returning to simpler interventions designed for self-use — interventions demonstrated to “do more good than harm” — and reducing professional intervention “to the minimum.”

The alternative, in his view, was to continue to acquiesce — with potentially fatal or disabling results — to a “planned and engineered Hell.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

August 26, 2022 Posted by | Science and Pseudo-Science, Timeless or most popular, War Crimes | , | Leave a comment

COVID-19 Vaccines and Informed Consent

The fundamental right to make decisions about bodily health and medical treatments

By Robert W Malone MD, MS | August 25, 2022

By way of introduction, this substack is written by Mr. Allison (JD). Mr Allison read my lawsuit against the Washington Post and was deeply offended by how the Washington Post has defamed me. So much so, that he wrote to my attorney with his research/analysis regarding the mRNA COVID-19 vaccines and informed consent. The review of the literature is so outstanding, that I asked if I could share it here.

This analysis is long – 53 pages long. It is Mr. Allison’s analysis – not mine, the analysis and opinions in this article are his alone.

I have only published the top level analysis (6 pages) here. The rest of the document, which is extensively referenced can be found by clicking the link below:

COVID-19 Vaccines and Informed Consent

By John Allison, J.D. Updated July 18, 2022

Introduction.

Most Americans have long assumed that they have a fundamental right to make decisions about their own bodily health and the medical treatments they receive. Informed consent is the ethical and legal principle by which that fundamental right is enforceable. To be able to give informed consent a person needs to be informed about the risks and benefits of, and alternatives to the proposed treatment.

The fundamental right to informed consent is particularly important with respect to the COVID-19 vaccines which are available in the United States pursuant to Emergency Use Authorizations (EUAs). Under the federal EUA statute, people are entitled to be informed about their right to accept or refuse administration of these vaccines, the consequences (if any) of refusing vaccination, and the benefits and risks of alternatives to the vaccines. The manufacturers of EUA vaccines, and the people and organizations administering them, are immune from liability suits. People who suffer severe adverse effects after receiving a COVID-19 vaccine will not be able to recover compensation, for their monetary and emotional distress damages, from the vaccine manufacturers or from the people who vaccinated them. Similarly, the family members of people who die after receiving a COVID-19 vaccine will not be able to recover compensation for their loss.

Qualifications and Experience.

I am a retired lawyer, licensed to practice in Washington State and the District of Columbia, with extensive private law firm and in-house experience. Most of my law practice was devoted to the litigation of cases involving medical, toxicological, industrial hygiene and product safety issues. In my in-house role I was Assistant General Counsel in the legal department of a Fortune 100 company with overall responsibility for product liability, environmental and commercial litigation. I was also the lawyer for the company’s Medical Department, including Corporate Toxicology, Epidemiology and Product Responsibility.

This memorandum presents the results of research I performed and my opinions based on that research. This memorandum is not intended to give legal advice. People who want legal advice on the issues raised in this memorandum should consult with a lawyer licensed to practice in their jurisdiction.

Opinions.

Based on the results of my research to date, I have arrived at the following opinions with respect to the COVID-19 vaccines currently authorized or approved for use in the United States:

1. Government misinformation about the safety and effectiveness of the COVID- 19 vaccines, censorship of credible scientific and medical information about the risks of death and serious adverse effects of the COVID-19 vaccines, and vaccination coercion, are depriving people of their ability to give informed consent to vaccination. Unless the limited effectiveness of the vaccines and the risks of death and serious adverse effects described in this memorandum are disclosed to people before they are vaccinated, informed consent has not been obtained.

2. Safe and effective drugs on the market for many years, such as ivermectin and hydroxychloroquine, have been proven by reputable doctors to be successful in the early treatment of COVID-19. If those affordable drugs had been allowed to be more widely used in the United States before people needed to be hospitalized, many tens of thousands of people who died from COVID-19 would probably be alive today.

3. The COVID-19 vaccines authorized or approved for use in United States do not meet established criteria for establishing their short-term and long-term safety and efficacy. Serious safety signals – red flags – about these vaccines have been ignored, and continue to be ignored, by the FDA and the CDC. The EUAs for the Pfizer-BioNTech, the Moderna and the Johnson & Johnson/Janssen COVID-19 vaccines, and the FDA’s approval of Pfizer’s Comirnaty vaccine and Moderna’s Spikevax vaccine, should be revoked. All of these vaccines should be taken off the market immediately.

  • SARS-CoV-2 is the coronavirus that causes COVID-19. Distinctive spike proteins on the surface of the virus enable the virus to penetrate cells and cause infection. The spike proteins mutate, producing the Delta variant which became the dominant form of the virus by the middle of 2021. Continuing mutations of the spike protein produced the Omicron variant which became the dominant form of the virus by the end of 2021. We are now dealing with sub- variants of Omicron.
  • The first confirmed case of COVID-19 in the United States was reported in mid-January, 2020. The pandemic spread. COVID-19 vaccines were not available until the middle of December 2020 when the FDA granted emergency use authorization for the Pfizer- BioNTech and the Moderna vaccines. In February 2021 the FDA granted emergency use authorization for the Johnson & Johnson/Janssen vaccine. Early in 2021 these vaccines became widely available in the United States and mass vaccination programs began. By the middle of 2021 millions of Americans, including workers in many different occupations, were fully vaccinated.
  • The COVID-19 vaccines do not produce immunity to COVID-19 because they are not designed to trigger an immune response to the SARS-CoV-2 virus. Instead, the vaccines are designed to trigger an immune response to the spike proteins on the surface of the original virus.
  • A number of studies demonstrate that the vaccines do not prevent infection or transmission of COVID-19. Fully vaccinated people can become infected and can also spread the SARS-CoV-2 virus to other vaccinated people and to unvaccinated people.
  • According to data on the CDC website, in the United States there were 385,670 deaths attributed to COVID-19 in 2020, before the vaccines were widely available. In 2021, when vaccines were widely available and mass vaccination campaigns took place, there were 463,210 deaths attributed to COVID-19 – an increase of 20.1%.
  • When the Delta and later the Omicron variants became the dominant form of the virus, government studies in different countries show that most COVID-19 hospitalizations and deaths occur among fully vaccinated people.
  • Now that the Omicron variant is the dominant form of SARS-CoV-2, the effectiveness of the mRNA vaccines (Pfizer and Moderna) diminishes significantly over just a few months. According to a Danish study, which has not yet been peer reviewed, vaccinated people, more than 90 days after vaccination, are more likely than unvaccinated people to be infected by Omicron.
  • The COVID-19 vaccines contain genetic instructions that cause the body to produce enormous numbers of SARS-CoV-2 spike proteins in order to provoke an immune response to the spike proteins. Unfortunately, it turns out that the spike proteins, themselves, are toxic to cells. For example, endothelial cells line the inside of arteries to make blood flow smoothly. Damage to the endothelial cells caused by spike proteins increases the potential for microscopic blood clots to form. Those microscopic blood clots can travel to the lungs, increasing the risk of developing arterial hypertension which is a serious progressive condition that overtaxes and weakens the heart. There is no known cure for that condition.
  • In the mRNA COVID-19 vaccines manufactured by Pfizer and Moderna the genetic instructions that cause the body to produce spike proteins are encapsulated in lipid nanoparticles. A preclinical study on laboratory animals conducted by Pfizer shows that the lipid nanoparticles and mRNA genetic instructions enter the bloodstream and accumulate in several organs, including the spleen, bone marrow, liver and adrenal glands, and concentrate in the ovaries. The body then starts producing spike proteins wherever the mRNA genetic instructions happen to land.
  • A number of serious medical conditions have been associated with the COVID-19 vaccines, including blood clotting disorders, cardiac emergencies, myocarditis, Guillain-Barré Syndrome, autoimmune disease, spontaneous miscarriages, nervous system disorders and female infertility.
  • The COVID-19 vaccines also interfere with the natural immune system, making a person more susceptible to viral infections and cancer. This may explain why most COVID-19 symptomatic infections, hospitalizations and deaths are now occurring among fully vaccinated people.
  • A recent laboratory study in Sweden indicates that the Pfizer- BioNtech COVID-19 vaccine is able to enter a human liver cell line where it is reverse transcribed into DNA within a matter of hours. As a result, the possibility that the COVID-19 vaccines affect DNA cannot be ruled out.
  • The mRNA COVID-19 vaccines also contain problematic ingredients. Both the Pfizer and the Moderna vaccines contain polyethylene glycol (PEG) as an active ingredient. An Expert Panel assessing the safety of PEG recommended against using PEG in ointments applied to damaged skin because some burn patients treated with a PEG-based antimicrobial cream experienced renal tubular necrosis and died of kidney failure. The PEG used in the Moderna vaccine matches the description of a PEG product manufactured by Sinopeg, a company in China. According to the Sinopeg website, that product is for “research use only.” The Moderna vaccine also contains a lipid known by the trade name SM-102. The Pfizer vaccine also contains a lipid known by the trade name ALC-0315. According to the safety information on the website of Cayman Chemical Company, which manufactures SM- 102 and ALC-0315, both of those products are “for research use – Not for human or veterinary diagnostic or therapeutic use.” Yet, in the mRNA COVID-19 vaccines, PEG, SM-102 and ALC-0315 are being directly injected into people’s bodies.
  • Because no long-term clinical studies were performed, there is no way of knowing whether or not vaccinated people will suffer severe adverse side effects in the future. This is a significant concern, since the vaccines increase the potential for developing cardiovascular disease and autoimmune disease, which can both take months or years to develop.
  • In 1990 the government established the Vaccine Adverse Events Reporting System (VAERS) which is co-managed by the CDC and the FDA. It is intended to be a national early warning system to detect possible safety problems with vaccines in the United States. The number of serious adverse events and deaths that have been reported in VAERS for the COVID-19 vaccines is many times greater than the serious adverse events and deaths reported in VAERS for all other vaccines combined. As of July 1, 2022 more than 29,200 deaths, and more than 212,600 serious injuries, following administration of one of the COVID-19 vaccines have been reported in VAERS. Yet the CDC and the FDA continue to ignore these serious safety signals.
  • In contrast, in 1976 the federal government conducted a mass vaccination campaign against the swine flu. After roughly 25% of the population in the United States had been vaccinated, the government terminated the vaccination program due to reports of 25 deaths and 550 cases of Guillain-Barré Syndrome following vaccination.
  • According to a mortality analysis by the Johns Hopkins Coronavirus Resource Center, 98.9% of all the people in the United States with a confirmed case of COVID-19 survived the disease. Most COVID-19 deaths occurred in elderly people who were in poor health with multiple comorbidities.
  • The Society of Actuaries collected and analyzed claims data from twenty life insurance companies that provide group term coverage in the United States, representing roughly 90% of the employer-based group term life insurance industry. All-cause mortality data for the pandemic period (April 1, 2020 through September 30, 2021) was compared to all cause mortality data for the baseline period (2017 through 2019). The analysis reveals a dramatic spike in deaths from all causes during the third quarter of 2021 (July 1 through September 30). During that quarter, excess mortality for all policyholders was more than 30% above baseline. The spike in deaths was even more dramatic for working-age people. Excess mortality for people ages 25 to 34 was 81% above baseline, excess mortality for people ages 35 to 44 was 117% above baseline, excess mortality for people ages 45 to 54 was 108% above baseline, and excess mortality for people ages 55 to 64 was 70% above baseline. The dramatic increase in deaths from all causes during the third quarter of 2021, particularly among working age people, undermines the claim that the COVID-19 vaccines are safe and effective… 

    Continued in the PDF link below

 

COVID-19 Vaccines and Informed Consent

 

I encourage everyone to to read more of this analysis by Mr. Allison. It will be well worth your time.

August 26, 2022 Posted by | Civil Liberties, Science and Pseudo-Science, Timeless or most popular | , | Leave a comment

DC Mayor: No vaccine passport, no education – even for virtual learners

By Ken Macon | Reclaim The Net | August 26, 2022

The District of Columbia mayor Muriel Bowser said kids who do not have a vaccine passport within the first 20 days when schools resume next week Monday will not be allowed to get educated, even for those doing virtual learning from home.

A press release on the District of Columbia Public School’s website states: “The Coronavirus Immunization of School Students and Early Childhood Workers Amendment Act of 2021, which the Council passed in 2021, requires students ages 12 and older to be vaccinated against COVID-19 in order to attend school.”

The vaccine mandate applies to staff and also private schools.

Asked by The Daily Signal what the plan was for unvaccinated students, Bowser said: “They can go to school on Monday. But they need to get their vaccinations… and their families will be alerted as to the dates.”

The Office of The State Superintendent of Education for the District of Columbia recently announced that “all students must have up-to-date immunization certification on file with the school within the first 20 school days or they will not be allowed to attend school or school activities until the immunization certification is secured by the school.”

“If the student does not come into compliance within a 20-school day period, the school must remove the student from school until the immunization certification is secured by the school,” the office added.

The vaccine mandate will likely affect the education of black students as 47% of black children aged 12-15 in DC have not received the primary vaccination needed to attend school, according to government data. And 42% of black kids aged 16 and 17 are not vaccinated.

August 26, 2022 Posted by | Civil Liberties, Science and Pseudo-Science, Subjugation - Torture, War Crimes | , , | Leave a comment

CDC Director deflects blame for lockdowns towards predecessors

By Mike Campbell | The Counter Signal | August 25, 2022

CDC Director Rochelle Walensky admitted organizational shortcomings on Fox News while deflecting blame toward predecessors for their lockdown recommendation.

“Many of those lockdowns pre-dated me at the CDC,” she said.

Walensky, who once used ‘Trust the science’ to persuade the public, carried a humbler tone while reflecting on her organization’s decisions.

“There were important decisions that we had to make in imperfect times, with imperfect data, and we always updated those decisions as those data were evolving…”

“So, I don’t really want to re-visit the questions of lockdowns that pre-dated me, but what I will say is, we’ve updated our guidance in the context of new information, and sometimes we have to make a decision before we have all the information that we want…”

Indeed, the CDC updated guidance by removing special quarantine recommendations for unvaccinated persons, effectively admitting that vaccination status is no longer relevant when it comes to infection or spread of the Covid virus.

In fact, on July 23, the CDC deleted a ‘fact’ from their “Facts about mRNA Covid-19 Vaccines”, and they did so without explanation. Last time I checked, facts don’t change — but apparently, they do for the CDC.

Walensky further stated that “[their] science” indicated hybrid immunity was superior to natural immunity. However, we’ve reported on a scientific study that accounted for more than 5.7 million people, which showed that natural immunity is just as effective as hybrid immunity.

To this point, Walensky’s usage of science in the possessive sense — by calling it “our science” — denotes a departure from “the science,” of which they’re either arbitrarily picking from or are completely unaware.

Between Fauci stepping down and Walenski pointing fingers, it appears the blame game has officially started.

August 25, 2022 Posted by | Civil Liberties, Science and Pseudo-Science | , , , , | Leave a comment

Watch the New Film About Cartoonist Bob Moran

BY TOBY YOUNG | THE DAILY SCEPTIC | AUGUST 22, 2022

A talented filmmaker called Keith Craig has made a film about Bob Moran, the brilliant, acerbic, passionate cartoonist who lost his job at the Telegraph for being too outspoken and uncompromising in his opposition to the lockdown policy. Most of this site’s long-term readers will be familiar with Bob’s work, which we have used many times and continue to use in our Archive section. They’ll also be familiar with the cast of talking heads in this film – James Delingpole, Bev Turner, Dr. Tess Lawrie, Bernie Spofforth, Tonia Buxton and more.

This hugely enjoyable, lovingly-made film is very much worth watching in full. Deserves to become a cult classic.

August 25, 2022 Posted by | Civil Liberties, Science and Pseudo-Science, Timeless or most popular, Video | , , , | Leave a comment

The latest on vaccination of 5-11 year-olds

When will the onslaught on children end?

Health Advisory & Recovery Team | August 23, 2022

In February 2022, the JCVI in their wisdom, made a ‘non-urgent offer’ of Covid-19 vaccination for healthy children aged 5-11, scheduled to begin in April. It is worth reading the full statement, which hardly makes a strong case. Here are a few quotes.

  • In comparison to the rest of the population / older age groups, evidence indicates that children aged 5 to 11 are at the very lowest risk from COVID-19. Rates of hospitalisation, paediatric intensive care admission and death are lower in this age group than in all older age groups. In addition, the high level of prior infection in this age group of children can be expected to contribute towards their natural immunity against reinfection. There are some data to suggest that natural immunity may last longer than vaccine-induced immunity against non-severe infection.
  • The impact of vaccination on school absences was indeterminate; the balance between school absences due to reactions following vaccination versus school absences avoided due to prevention of infection is highly influenced by the uncertain timing of any future wave of infection and of the vaccination programme.
  • vaccine effectiveness against symptomatic infection due to Omicron (Pfizer-BioNTech vaccine) wanes over time from around 70% shortly after 2 vaccine doses to around 25% after 10 weeks and 10% after 20 weeks.
  • [myocarditis] medium to long-term (months to years) prognosis remains less certain.
  • It is estimated that over 85% of all children aged 5 to 11 will have had prior SARS-CoV-2 infection by the end of January 2022

This last point makes the programme for this age group even more ridiculous – the 85% estimate of January 2022 has now risen to 99%, and is perhaps the main reason why parents have not been clamouring to get their children vaccinated (10% to date). Despite this, the government is planning an enhanced programme this September to reach all the currently unvaccinated, in particular primary school children.

Cornwall and the Isles of Scilly (NHS Kernow) are leading the way with advertisements and pop up clinics because of ‘a rise in cases’. As previously, petting dogs have been enrolled, and advertisements such as the one pictured here, are falsely claiming that somehow vaccinating small children who are already immune, will magically protect their grandparents.

Legal challenges: Meanwhile, disappointingly though not surprisingly, the Court has thrown out the request for a judicial review of the MHRA, the JCVI, and Secretary of State’s decision to vaccinate this age group and for the 12-15s another judge likewise rejected the legal challenge. A member of the legal team involved has published his response to these judgements here but in effect both judges were saying that the MHRA, the JCVI and the CMOs are self-evidently “experts”, thus the Secretary of State is clearly acting correctly to accept their advice, irrespective of whether their advice is sound. This is a bad day for UK citizens since it appears that drug regulators are now unaccountable.

The political route: The Children’s Covid Vaccines Advisory Committee (CCVAC) who helped with these cases, have recently sent a summary of all their concerns to Stephen Barclay, the latest Secretary of State for Health & Social Care. A reply has been received giving the usual bland “Vaccines are now safer than ever before.” and quoting the same data presented by the JCVI a year ago, totally failing to grasp that the current data give a very different risk:benefit balance. The CCVAC team have also drafted a letter for the new Prime Minister and they are seeking health professionals to add their signatures ready to have a very large letter to deliver to the new incumbent of No 10 in early September. The letter calls on the Prime Minister to halt the vaccination of children pending a full and independent safety review. Is there any chance that the new British Prime Minister will follow the lead taken by several Scandinavian countries? The Director of Denmark’s Board of Health for example was recently on record saying that the vaccination of children had achieved nothing. Meanwhile a report from Iceland shows that in their ~60,000 child population, serious vaccine injuries (eleven) far outweighed Covid-19 hospital admissions (zero).

Readers are invited to share this letter with any health professionals they know, including staff at their local medical centre.  Letter to incoming PM: apply the precautionary principle (childrensunion.org)

August 24, 2022 Posted by | Science and Pseudo-Science, Timeless or most popular, War Crimes | , | Leave a comment

Too Little Too Late: WSJ Tries to Save Face on Failed COVID Policies

By Madhava Setty, M.D. | The Defender | August 23, 2022

The Wall Street Journal last week published an opinion piece, “Fauci and Walensky Double Down on Failed Covid Response,” with this subhead: “Lockdowns were oppressive and deadly. But U.S. and WHO officials plan worse for the next pandemic.”

The article begins:

“The Centers for Disease Control and Prevention [CDC] belatedly admitted failure this week. ‘For 75 years, CDC and public health have been preparing for Covid-19, and in our big moment, our performance did not reliably meet expectations,’ Director Rochelle Walensky said. She vowed to establish an ‘action-oriented culture.’”

Yes, you read that correctly. Dr. Anthony Fauci and Walensky admitted they failed. They learned their lesson.

As John Tierney, author of the op-ed, wrote:

“Lockdowns and mask mandates were the most radical experiment in the history of public health, but Dr. Walensky isn’t alone in thinking they failed because they didn’t go far enough. Anthony Fauci, chief medical adviser to the president, recently said there should have been ‘much, much more stringent restrictions’ early in the pandemic.”

They believe that they didn’t go far enough? There should have been “much, much more stringent restrictions?”

That’s what they learned from the destruction their public health policies wreaked upon this nation and the others that followed their lead?

To his credit, Tierney pointed out the absurdity of Walensky’s and Fauci’s stance on their own incompetence.

Tierney also dropped a series of “truth bombs,” including:

  • “Their oppressive measures were taken against the longstanding advice of public-health experts, who warned that they would lead to catastrophe and were proved right.”
  • “For all the talk from officials like Dr. Fauci about following ‘the science,’ these leaders ignored decades of research — as well as fresh data from the pandemic — when they set strict Covid regulations.”
  • “The burden of proof was on them to justify their dangerous experiment, yet they failed to conduct rigorous analyses, preferring to tout badly flawed studies while refusing to confront obvious evidence of the policies’ failure.”
  • “U.S. states with more-restrictive policies fared no better, on average, than states with less-restrictive policies.”
  • “When case rates throughout the pandemic are plotted on a graph, the trajectory in states with mask mandates is virtually identical to the trajectory in states without mandates. (The states without mandates actually had slightly fewer COVID deaths per capita.)”
  • A Johns Hopkins University meta-analysis of studies around the world concluded that lockdown and mask restrictions have had “little to no effect on COVID-19 mortality.”
  • Florida’s and Sweden’s open policies have been vindicated based upon their lower levels of excess mortality compared to other regions.
  • “It was bad enough that Fauci, the CDC and the World Health Organization ignored the best scientific advice at the start of this pandemic. It’s sociopathic for them to promote a worse catastrophe for future outbreaks.”

I take no issue with Tierney’s list. The problem here is with the Wall Street Journal.

Every single point this opinion piece offered could — and should — have been made months or years ago.

There was longstanding advice from public health experts that predicted Fauci and Walensky’s failures? Why didn’t you say so in 2020?

Fauci and Walensky ignored decades of research? They touted flawed studies while ignoring the obvious failures unfolding in front of them, month after month?

The successes of Sweden and Florida were apparent in 2020.

Where were the articles in your publication that could have brought light to these issues over the last two years?

The Johns Hopkins University analysis on mask restrictions was published nearly nine months ago. Why didn’t you cover it?

Why did it take so long to run this kind of piece when the evidence was around for so long?

Do you really expect us to look the other way because you now have the temerity to call Anthony Fauci sociopathic?

You had ample opportunity to give voice to the dissenters who were pleading for a voice, a conversation and a debate based on the very same evidence you are mentioning now.

You failed your readership. You failed the public.

The CDC’s policies were so devastating because you did not challenge them. Not once.

As a media platform, you were no less negligent than the public health officials you see fit to denigrate now — after untold damage has occurred, at their hands and yours.

Perhaps you’ve caused your loyal readers to finally scratch their heads and reconsider their perspective after 28 months of mercilessly attacking those of us who were asking you and other mainstream platforms to do your job.

Why are you holding Fauci and Walensky accountable now? Is it because they are finally admitting they blew it?

They are not the only galactically incompetent parties in this global tragedy. You are, too. And we all know it.

Interestingly, your scathing attack on our public health agencies still hasn’t gone nearly far enough.

One of their biggest “blunders” was not around lockdown measures. It was the dismissal of powerful, early treatment regimens, including ivermectin, that could have saved thousands of lives or more.

Instead, the public was forced to wait for a largely ineffective and harmful vaccine that has since exacted an incalculable level of damage on humanity.

Nevertheless, more than a year after Dr. Pierre Kory gave impassioned congressional testimony demanding that an official expert panel be convened to examine the mountains of evidence coming from all corners of the globe demonstrating the significant benefits of ivermectin in treating and preventing COVID-19, you had the audacity to print this hit piece on the safe and effective medicine that would have obviated the need to inject poorly tested mRNA technology into the bodies of several billion human beings.

Beyond being irresponsible, the article was silly, citing a single, small and yet-to-be-published study (at the time) that purportedly showed no benefit as proof that ivermectin cannot prevent COVID-19 hospitalizations.

The study underdosed the participants and was too small to detect statistically significant benefits, despite reduced incidence of hospitalization in most cohorts that got the medicine. (Read a full critique of the study here).

The study didn’t prove anything — other than that it was designed to fail from its inception.

Talk about touting a “badly flawed” study.

More importantly, your article on the study missed the real story: the scuttling of ivermectin by an unseen hand that was, it seems, in the pockets of the Bill & Melinda Gates Foundation through Unitaid, a quasi-governmental advocacy organization the foundation funds (full story here).

Have your editors lost their sense of smell from repeated bouts of COVID-19? Or were you never able to sniff out where the real stories are?

It’s fairly obvious that despite this attempt to reclaim your journalistic integrity you are still muzzled. Any story that even intimates that the highly profitable COVID-19 vaccine was not only unnecessary but also a stark failure, is still off-limits.

Your silence on this continues to deafen us.

Madhava Setty, M.D. is senior science editor for The Defender.

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

August 24, 2022 Posted by | Mainstream Media, Warmongering, Science and Pseudo-Science, Timeless or most popular, War Crimes | , | Leave a comment

Inside the mind of one of my very smart pro-vax friends

If you ask them for data to back up their claims, they stop responding.

By Steve Kirsch | August 22, 2022

I recently talked to a friend of mine at a recent social event. We’ll call him Bob. He’s super smart about most things. But when it comes to the vaccine, he’s blind to the truth.

He was bragging about how he has been vaxxed 6 times with the COVID vax and he’s perfectly healthy. He can’t wait for SB 866 in California to pass so when his kids turn 12, they can decide to get the vaccine over their mother’s objections.

Bob thinks I’m a nut case, cherry picking data. He says I used to be respected, but after turning anti-vax, people have lost all respect for me. He said I have a religious belief about the vaccine and I’m not driven by data.

What he isn’t telling anyone is that he’s been losing his vision ever since he got his first COVID vaccine. He used to have 20/20 vision, but now he wears glasses and can’t drive at night. When I brought up the data showing the connection between the shots and vision loss, he changed the topic.

I showed him two papers showing the more you vaccinate, the sicker you get (see the two papers here). I asked, “Where are the papers that show the opposite?” He ignored my request.

He gets his belief system from the mainstream media. Full stop. He reasons that if I was correct, surely Bill Gates would agree with me and admit they goofed. It’s 100% deference to authority.

Bob will not look at the data himself and he doesn’t want to discuss it. He will not engage. He thinks that if I was right, there would be more than a handful of people speaking out. So he tallies the size of the support base on each side of an issue instead of looking at the data.

I hope this is useful in helping you understand the pro-vaxxers and how they think.

The important thing is you cannot turn these people around. Arguing with them is fruitless because they don’t want to see the data. They will only come around when the people they trust change their position.

This is why we need to focus on protecting doctors who speak out.

Perhaps a state ballot initiative in California providing that doctors cannot be retaliated against when they tell the truth (including having social media accounts taken down, having their license to practice medicine revoked, etc). That would prevent things like this from ever happening again.

August 23, 2022 Posted by | Civil Liberties, Science and Pseudo-Science, Timeless or most popular | | Leave a comment

Untested Bivalent COVID Jab Being Rolled Out

Video Link

By Dr. Joseph Mercola | August 22, 2022

August 15, 2022, the U.K. became the first country to approve Moderna’s new bivalent COVID booster, which contains both the original concoction and mRNA to target Omicron variants. The booster has also been submitted for approval with authorities in Australia, Canada and the EU, and there’s every reason to suspect it’ll be submitted to the U.S. Food and Drug Administration as well. As reported by Sky News:1

“The booster dose, known as ‘Spikevax bivalent Original/Omicron,’ contains 25 micrograms of Omicron vaccine and 25 micrograms of original coronavirus vaccine …

The Joint Committee on Vaccination and Immunization (JCVI) has said the vaccine will be available to those aged 18 and over as part of the UK’s autumn booster program. Health Secretary Steve Barclay said those eligible will be contacted from early September.”

More Than 100 Million Doses Have Been Trashed

The approval of the new booster comes right on the heels of widespread complaints about lack of demand for the shots. Moderna recently had to throw away 30 million doses of its original COVID jab, as there was no demand for them.2

“We have a big demand problem,” Moderna CEO Stéphane Bancel said in May 2022 during a panel discussion at the World Economic Forum’s meeting in Davos, Switzerland.3 Similarly, in the U.S., pharmacies, states and federal agencies have tossed 82.1 million COVID jab doses in the trash, and for the same reason.4

Bivalent Booster Is Already Out of Date

Moderna’s bivalent booster is said to “provide a strong immune response against the Omicron BA.1 variant as well as the original 2020 Wuhan strain,” which, for the record, is extinct and no longer in circulation anywhere in the world. BA.1 is now rarely ever found, either.

The graph5,6 below, from the U.S. Centers for Disease Control and Prevention, shows the infection ratios of common variants. As you can see, in the U.S., infections are now caused by the BA.4, BA.5 and BA.2.12.1 variants of Omicron.7 So, this booster contains two strains that aren’t even relevant anymore.

The situation is exactly the same in Europe, where Omicron BA.2, BA.4 and BA.5 are the current “variants of concern.” BA.1 isn’t even a “variant of interest,” which is the next-lower categorization. It’s on the list of “de-escalated variants,” which is based on a variant meeting one or more of the following criteria:8

“(1) the variant is no longer circulating, (2) the variant has been circulating for a long time without any impact on the overall epidemiological situation, (3) scientific evidence demonstrates that the variant is not associated with any concerning properties.”

In short, BA.1 is of no concern in Europe either, as it’s not in circulation and/or because it doesn’t cause severe illness. The same goes for the original Wuhan strain, which has long since mutated out of existence.

Vaccinating Against Rapidly Mutating Viruses Is a Bad Idea

Coronaviruses mutate very rapidly in general, and the mRNA jabs are based on a surface protein (the spike protein), which is the most rapidly mutating portion of the entire virus. What happens when you vaccinate against a rapidly mutating virus? You encourage it to mutate even faster, and to develop immune-evading properties.

This is what we’ve been witnessing since the beginning of the COVID jab campaign, and at this point, there’s no hope of ever catching up with the virus. What’s worse, while variants have so far evolved into milder strains, they are in fact gaining the ability to evade antibodies, and could theoretically switch course to become more pathogenic.9

This is particularly true when a vaccine is “leaky,” meaning it doesn’t fully prevent infection (which none of the COVID shots do). Just like when you overuse an antibiotic that fails to eradicate the bacteria, which allows antibiotic-resistant bacteria to flourish, overuse of a leaky vaccine can pressure a virus to become more lethal.10,11

BA.4 and BA.5 are the most resistant to date, with BA.5 circumventing the immune systems even of those with natural immunity.12 Fortunately, it doesn’t appear to cause severe illness in most people.

The take-home here is that had natural immunity been allowed to take place without these jabs, the pandemic would be over and reinfections near-nonexistent. Instead, we’re now in a pandemic of the vaccinated, with the vast majority of serious COVID infections occurring among those who have been jabbed.13,14

We know that Pfizer was aware of this possibility, as “vaccine-associated enhanced disease (VAED)” is listed as an “Important Potential Risk” in Table 5 on page 11 of a document called “5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports.”15 This document was part of the FOIA required and court-ordered batch released by the FDA April 1, 2022.

How Long Will the Bivalent Booster Protect You?

According to Moderna, the bivalent Spikevax “demonstrates potent neutralizing antibody response against Omicron subvariants BA.4 and BA.5.”16 They made the same claim for the original COVID jab, back in January 2021,17 and by August 2021, they admitted the neutralizing antibodies generated lasted only six months after the second dose.18

How long will the bivalent jab “be effective” (and I use that term loosely)? Who knows, but the way things are trending, six months would probably be the max. In Germany, citizens must now get a booster every three months to qualify as “fully vaccinated,”19 as rapidly waning immunity has become accepted fact, and that’s probably where we’re all headed.

Germans who haven’t received all of their boosters will be subject to mask mandates and other COVID restrictions this fall. This, despite deep criticism from businesses tasked with confirming their customers’ status. As reported by the Rise Align Ignite Reclaim (RAIR) foundation:20

“Businesses have voiced great concern about further regulatory chaos in the struggling economy. ‘The plans are simply not feasible,’ said the general manager of the German Hotel and Restaurant Association (Dehoga), Ingrid Hartges, the Handelsblatt. ‘We cannot constantly check whether our guests are vaccinated, recovered, or tested.’

These people are exempted from the obligation to wear masks in restaurants or events under certain circumstances — if the vaccination, for example, is within the last three months. ‘But you can’t tell from the guest in the restaurant what status they have,’ says Hartges. ‘Like when he goes to the bathroom — should the staff always ask if he’s vaccinated?’ she said. ‘That’s nonsense.'”

Bivalent Jab Will Not Undergo Additional Testing

It’s important to realize that these “next-gen” boosters will not undergo any additional safety testing.21,22 They’re being rolled out under a new fast-track standard where ingredients can be swapped out without additional testing.

This is the standard protocol for seasonal flu vaccines. However, we’re now using an entirely new type and essentially untested technology. There’s no telling whether variations in the spike mRNA being injected might produce vastly differing side effects. They could potentially have differing toxicities, but that’s not being investigated.

Also, remember that the “efficacy” they’re referring to is only based on measurements of antibody titers, which tells us nothing, really, about its ability to prevent infection, severity of illness or death. Why?

Because antibodies form only a part of your immune response, and they’re not even the most important. It is far more likely that your innate immune system — your first line of defense — will destroy a virus before your adaptive immune system even has a chance to respond and create antibodies.23

It is important to understand that no vaccine improves your innate immune response. All vaccines are ever able to do is address your adaptive humoral immune system and create antibodies. Your innate immune system has T cells that can directly kill viruses. If you happen to have a vigorous T cell response, you’ll be protected even if your antibodies are low. So, antibodies are not a necessary measure of immunity.

Antibody titer levels are what’s called a “surrogate outcome.” It’s a substitute for actual clinical outcome. But it’s in no way equivalent, no matter how much the powers in control want it to be. Antibody titers may be high, but in the real world, more people may end up in the hospital and die — either from the infection or from the shot. In short, high antibody titer is not a guarantee of effectiveness — and it tells us absolutely nothing about safety.

CIA-Backed Upstart to Produce Moderna’s Bivalent mRNA

The complete absence of testing moving forward is all the more concerning when you consider who’s manufacturing the RNA for Moderna’s now-bivalent booster. In a recent Unlimited Hangout article,24 investigative journalist Whitney Webb reveals the genetic material for the reformulated booster is being exclusively manufactured by National Resilience, a relative newcomer with significant ties to U.S. intelligence agencies.

Its board of directors include In-Q-Tel CEO Chris Darby, who is also on the board of directors of the CIA Officers Memorial Foundation, and former FDA commissioner and Pfizer board member Dr. Scott Gottlieb. Not surprisingly, National Resilience promises to successfully lead its customers through the government regulatory process. As reported by Webb:25

“National Resilience was founded … in November 2020, and … plans to ‘reinvent biomanufacturing’ and democratize access to medicines,’ namely gene therapies, experimental vaccines and other ‘medicines of tomorrow’ …

In April 2021, National Resilience acquired Ology Bioservices Inc., which had received a $37 million contract from the US military the previous November to develop an advanced anti-COVID-19 monoclonal antibody treatment. This acquisition also provided National Resilience with its first Biosafety Level 3 (BSL-3) laboratory and the ability to manufacture cell and gene therapies, live viral vaccines and vectors and oncolytic viruses.

Despite being in the earliest stages of developing its ‘revolutionary’ manufacturing capabilities, National Resilience entered into a partnership with the Government of Canada in July of last year. Per that agreement, the Canadian government plans to invest CAD 199.2 million (about $154.9 million) into National Resilience’s Ontario-based subsidiary, Resilience Biotechnologies Inc.

Most of those funds are destined for use in expanding the Ontario facility that Resilience acquired last March and which is now manufacturing the mRNA for Moderna’s COVID-19 products … More recently, in 2022, the company has announced a few new clients – Takeda, Opus Genetics and the US Department of Defense …

Considering Moderna’s history and Resilience’s connections, there may be more to this partnership that meets the eye and concerned members of the public would do well to keep a very close eye on Resilience, its partnerships, and the products it is manufacturing.

Given that we now live in a world where government regulatory decisions on the approval of medicines are increasingly influenced by corporate press releases and normal regulatory procedures have fallen by the wayside for being too ‘slow,’ there is likely to be little scrutiny of the genetic material that Resilience produces for the ‘medicines of tomorrow.’

This seems to be already true for Moderna’s recently retooled COVID-19 vaccine, as there has been no independent examination of the new genetic sequence of mRNA used in the Omicron-specific vaccine candidate or its effects on the human body in the short, medium or long term.

For those who are skeptical of the outsized role that intelligence-linked companies are playing in the attempted technological ‘revolution’ in the medical field, it is best to consider Resilience’s role in the upcoming fall vaccination campaign and in future pandemic and public health scenarios before trying its ‘futuristic’ products.”

Was COVID Jab Intentionally Flawed?

Video Link

In a June 2022 interview with British radio presenter Maajid Nawaz, Michael Yeadon, Ph.D., a former vice-president and chief scientific adviser for Pfizer and founder/CEO of the biotech company Ziarco (now owned by Novartis), explained why he believes the COVID jabs were intentionally made to be harmful and to prolong the pandemic.

For starters, it’s been known for more than 10 years that spike protein causes adverse effects in humans,26 so this could not be a design error. It must have been intentional.

As Yeadon explained, when making a vaccine, you have to be very careful about which part of the virus you use, as certain parts are more toxic and some provoke better immune responses than others. “What you would do is ask, ‘What’s the toxicity of the bit I’m going to give a person?'” he said.

Seeing how scientists have known for at least a decade that spike protein from related viruses causes blood clots through at least two different mechanism, the choice to use mRNA that programs your cells to make spike protein raised a warning flag from the start.

Nothing About the COVID Jabs Makes Sense

In addition to that, 90% of the immune response you get from natural COVID infection is in response to other parts of the virus, not the spike protein. Put another way, exposure to spike protein mounts an inferior immune response. If you’re looking to make an effective vaccine, wouldn’t you choose a part of the virus that mounts the best and most robust immune response?

By choosing the spike protein on which to base COVID-19 shots, scientists picked a protein that a) was known to be toxic to humans and b) produced an inferior immune response (compared to other parts of the virus).

On top of that, spike protein mutates rapidly, which destroys any protection the shot provides shortly after it’s given. As noted by Yeadon,27 “What you should do is pick the bits of the virus that’s genetically most stable,” but they didn’t do that. Why not? The end result is a seemingly never-ending series of boosters, and according to Yeadon, that may have been the plan from the start.

As if all of that weren’t enough, the spike protein is also similar to a variety of human proteins, which can trigger your body to mount an inappropriate immune response against your own proteins. In other words, it can cause autoimmune disease. Yet, scientists chose the spike protein anyway — even though it violated all of the accepted rules for creating a safe and effective product.

Collusion to Cause Harm

Yeadon believes the decision to use spike protein was not a mistake at all. He believes it was intentionally chosen because it has all of those ill effects. He told Nawaz:

“Again, you deselect things that are toxic in their own right, you pick things that are genetically stable, and you pick things that are most different from humans …

But guess what? Moderna picks spike protein and so does Pfizer, and AstraZeneca, and Johnson & Johnson. So, I put it to you, colleagues, any scientists out there or just logical people. How the hell would they pick [the spike protein]?

No team I was ever part of would ever have picked bloody spike protein for this vaccine. And you know what? If we did, and we have competing groups, we would not, all four of us, make the same mistake. Not possible. It’s collusion and malfeasance. The did it on purpose, knowing it would hurt you.”

Resources for Those Injured by the COVID Jabs

If you got one or more jabs and suffered an injury, first and foremost, never ever take another COVID booster, another mRNA gene therapy shot or regular vaccine. You need to end the assault on your system. The same goes for anyone who has taken one or more COVID jabs and had the good fortune of not experiencing debilitating side effects.

Your health may still be impacted long-term, so don’t take any more shots. When it comes to treatment, there are still more questions than answers, and most doctors are clueless about what to do — in part because they never bothered to give early treatment for COVID and therefore don’t understand how different medicines and supplements impact the spike protein.

So far, it seems like many of the treatments that worked against severe COVID-19 infection also help ameliorate adverse effects from the jab. This makes sense, as the toxic, most damaging part of the virus is the spike protein, and that’s what your whole body is producing if you got the jab.

Two doctors who have started tackling the treatment of COVID jab injuries in earnest include Dr. Michelle Perro (DrMichellePerro.com), whom I’ve interviewed on this topic, and Dr. Pierre Kory (DrPierreKory.com).

Both agree that eliminating the spike protein your body is now continuously producing is a primary task. Perro’s preferred remedy for this is hydroxychloroquine, while Kory typically uses ivermectin. Both of these drugs bind and thereby facilitate the removal of spike protein.

Kory also believes there may be ways to boost the immune system to allow it to degrade and eventually remove the spike from your cells naturally, over time. One of the strategies he recommends for this is TRE (time restricted eating), which stimulates autophagy, a natural cleaning process that eliminates damaged, misfolded and toxic proteins. Another strategy that can do the same thing would be sauna therapy.

As a member of the Front Line COVID-19 Critical Care Alliance (FLCCC), Kory helped develop the FLCCC’s post-vaccine treatment protocol called I-RECOVER. Since the protocol is continuously updated as more data become available, your best bet is to download the latest version straight from the FLCCC website at covid19criticalcare.com28 (hyperlink to the correct page provided above).

Sources and References

August 23, 2022 Posted by | Timeless or most popular, Video, War Crimes | | Leave a comment

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