What someone once said to me about vaccines, echoing Bill Gates

Dispatches from the vaccine war

by Jon Rappoport

July 19, 2023

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When I think about what piece to write next, or when for the moment my tank is empty, I come up with VACCINES. That’s the subject.

It’s been that way for a long time.

I could be accused of having a grand obsession, but this isn’t the case. I’m responding to the civilizational obsession with vaccination.

At the same time, it IS personal. Because of the outrage I feel, watching medical storm troopers who have been on the march for more than a hundred years.

Watching their arrogance, their blunt stupidity, their “rational” madness. As they keep marching and invading.

If we were living in an absolute monarchy and I were King, there would be hell to pay. The troopers would pay, dearly.

Over the past 35 years, I’ve written countless articles on vaccination. I’ve run down the evidence from all the angles. Now I’m left with the feeling when all the data detailing crimes have been exhausted. I’m at the end of that trail.

It’s not THE end, though. Not by a long shot.

The troopers and their allies represent, for me, everything that’s insane about our society—especially the bland acceptance by the willing victims. The silent majority.

Including, of course, the educated classes, who proudly wear their badges of science, the ultimate virtue signal. They live in a harsh bombed out desert and think it’s a pretty garden.

Some of them watch their children go crazy from the shots, suffering massive brain damage—and still these parents won’t admit what happened.

They refuse to see what they saw.

—It might have been after a talk I gave. I had mentioned the fact that improved sanitation and nutrition in the West accounted for the decline in all sorts of illness—not the widespread introduction of vaccines.

The person said, “But for children who still can’t get nutritious food, vaccines protect them.”

It was a mindless “save the children” remark.

Of course, when the body’s defense is chronically deficient, a vaccine isn’t going to pump it up. Because there isn’t anything THERE to pump up. That’s a ridiculous fairy tale. And a vaccine isn’t food.

Bill Gates tried to pull off the same sort of nonsense, when he announced with great personal fanfare, that he’d just read a book about contaminated water supplies in the Third World—as if he’d just discovered what everyone else had known for 50 years.

So he said something like this: I saw that bad water accounted for horrific chronic diarrhea, a killer. We have to clean up the water. But meanwhile, my anti-diarrheal vaccine will help.

No it won’t. The sick child, who is wasting away, has no immune system left. The vaccine won’t build up what isn’t there.

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Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free emails here.

The Babies and The Vaccine

Protecting your baby from a virus that doesn’t exist, with a killshot

by Jon Rappoport

June 16, 2022

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So you’ve had your eight-month-old baby injected with the COVID vaccine.

Of course.

And the SARS-CoV-2 virus doesn’t exist.

I’ve heard that. But it’s not the issue for us.

What is the issue for you?

Making a fashion statement.

How so?

We need to stay in the forefront of trends.

Why?

Why wouldn’t we?

Have you seen the federal database that records vaccine injury and death reports?

Of course.

So you know your baby could die from the shot.

Yes.

And that doesn’t matter to you.

Not as much as being able to tell our friends we had our baby vaccinated.

You, as parents—

That’s a misunderstood term. We don’t consider ourselves parents. The State is the parent. We’re the monitors.

Monitors?

We observe, and carry out limited functions.

Even if you assume the virus exists, the chances of your baby catching it and becoming ill are incredibly tiny.

That’s right. But this isn’t what we’re about. As I said, we’re keeping pace with fashion.

Are you human?

It depends on how you define the term. Humans are biological machines. Most people believe in something beyond that, but the content of belief is predetermined by a person’s upbringing, genes, conditioning, and so on.

Have you ever questioned vaccine science?

There’s nothing to question. We understand science. I have a PhD in psychology, and my husband is a software engineer. My IQ is 141. My husband’s is 136. We’re equipped to deal with vaccine issues.

If your baby died from the shot, would you mourn?

Yes. We would post photos and statements on our Facebook page.

—No doubt, some people would take offense at this “interview.” How could I? Here’s how. I wrote it. I wrote it because the government and Pfizer and Moderna—no matter how they interpret COVID and “the virus”—are moving ahead to inject as many babies as possible—which is a crime of mass assault and mass murder. Many parents will go along with it.


power outside the matrix

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Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

I don’t want half a revolution

Advice to reporters and others

by Jon Rappoport

May 5, 2022

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“I’m not anti-vaccine. I just want them to be safer and more effective.”

I love that statement. It’s a lullaby. When I can’t go to sleep at night, I just repeat it to myself a few times, and I’m out cold.

It’s typical of half a revolution, which never wins.

For the past 32 years, I’ve presented overwhelming evidence that no vaccine was ever safe or effective. The whole “science” of vaccination is a rank fraud.

But stuffed-shirt journalists, who sort of go against the grain while maintaining a front of respectability, don’t want to venture that far. They know the price they’ll have to pay. They’re hedging their bets.

Occasionally, one of them will take a swipe at me. It cements their position as middle of the road. Which is where they want to be.

Except, liberty and freedom, which is what we’re fighting for, against a global coup by mass medical murders, isn’t something you win in the middle of the road.

You don’t win by trying to come off like a Washington Post reporter who just happens to have different and dissenting ideas. That’s what half-ass looks like.

That sort of person is basically saying, “I have a machine mind like other machine minds. The difference is, I’m inputting different data and therefore drawing different conclusions. If you, too, have a machine mind, read what I write and let’s establish truth and justice…”

The long-term effect of that is like pissing through a fire hose to put out a conflagration taking down a city.

This is simple. If one group of “superior” machine minds wins against another group of machine minds—regardless of which issues come out on top—there is no revolution. LIFE AND FREEDOM have been excised out of the equation.

A considerable amount of money and effort have gone into building a modern culture composed of what looks like science and rationality, but isn’t. It’s a cartoon. A fucking cartoon.

There’s no JUICE in it.

That’s why I use the phrase machine-minds. Minds that calculate and process and collate and compare and then exude “better answers.” This is your educated class. Careful, cautious. Circumspect.

“Delivery, sir. Here are flowers you ordered. I’m sorry they’re dead.”

“I don’t mind dead. But I ordered roses and you brought me tulips. I can prove it. Let me just find the receipt here on my cell phone. And then I can show you these withered blossoms are actually tulips. There are 32 differences between the two types of flowers…”

That’s your educated class.

See, I’ve been at this for 38 years. Reporting. Writing. Actually, I’ve been writing for 66 years. I’ve made the cases I wanted to make. I’ve shoved the evidence in people’s faces. The overall medical cartel is waging a VERY successful war against the people.

You have to turn that evidence with torque, with leverage, into a flamethrower. You’re not just trying to set the record straight and bring in truth, you’re using the truth to crash the gold-plated systems of machine minds.

Those minds are remote. Distant. Distant is where Big Tech domeheads operate from. They profile, they plan, they crunch trillions of pieces of data, and they develop strategies to build a civilization that looks like their minds and their computers.

When one of these high-IQ blown dry characters develops his version of a conscience, and turns whistleblower, he’s a hero to his ilk. He speaks their language. He thinks the way they do. He geeks like they geek.

If I have to guess which guy has more freedom in his belly and his brain, I’m going with the man who lives up in the hills of Tennessee with a shotgun and a dog. If he doesn’t like what I’m writing, I might think about his reasons for a half-hour. Whereas, when an “alt. journalist” claims I’m “going too far,” I know exactly what his game is. He’s spraying his usual brand of sanitizing respectable room-deodorant.

I’ll put this another way. Two men are discussing how to choose a wife. They’re looking at two different lists of characteristics a man should consider and check. But neither man mentions LOVE, so it doesn’t matter which list they decide is superior. They don’t know what love is. What they’re really discussing are machine-thoughts.

If the COVID narrative had never been launched, if we were living now as we did in 2018, we would still have a medical cartel taking away our freedom and killing and maiming an extraordinary number of people. And that will still be the case, even if all COVID mandates and restrictions are defeated.

Plus, the Brave New World on the drawing boards is fronted by medical people. Three of its main features are genetic engineering, nanotechnology, and human-computer interfaces and hybrids. If you think all possible freedom is now under fire, you haven’t seen anything yet.

Way back when, I was briefly trained in two schools. The first was formal logic, taught by a beloved college professor with an extraordinarily sophisticated mind and a huge heart. The second school consisted of two or three encounters with Ida Honorof, activist and author. She was barely five feet tall, and she had the energy, in her 70s, of ten tigers. She explained to me one afternoon, on a street corner, that officials in Los Angeles were spraying a version of deadly Agent Orange in the Angeles National Forest. She handed me a few pounds of corporate and government documents detailing the massive toxicity of a variety of pesticides. She kick-started my life as a reporter.

Neither one of these people engaged in coddling. They didn’t sit around planning their fronts and poses of respectability. They didn’t want half a revolution. They didn’t equivocate.

I’ve never been a big fan of equivocation. I’m over at the I-don’t-give-a-shit end of the spectrum.

Find answers—then shove in all your chips. At the end of the night, don’t leave anything on the table.

Fortunately for all of us, there is a life after this one. But we’re here now, so we’re fighting.

Make it COUNT.

In the wind and the rain and the storm, issue no apologies.


The Matrix Revealed

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Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

Vaccines Beneath The Surface

by Jon Rappoport

April 27, 2022

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(Episode 6 of Rappoport Podcasts — “Kill-Shot Psychiatry, George Carlin, hero Peter Breggin; And the Real Drug War That Is Eating America” — is now posted on my substack. To listen, click here. To learn more about This Episode of Rappoport Podcasts, click here.)


The article below was a small section of my book, AIDS INC., which I wrote in 1987-8. At the time, I decided to take a look at vaccines and see what I could find out about them, because questions were being raised about the possible disease/toxic effects of a relatively new hepatitis-B vaccine, and its possible connection to AIDS.

My ensuing research led me into all sorts of surprising areas. These days, many people are seeing that the official position on vaccines is not the true story. So I thought I would reprint that section from AIDS INC. here.

Since the period of 1987-8, MUCH more has come to light about vaccine safety and efficacy. I’ve made no attempt to update my findings in a systematic way. They stand on their own, and reveal that, in the historical record, much has been lost, forgotten, and misplaced.


For years, critics on the fringes of medicine have pointed to problems with vaccines. It is generally acknowledged that, given to people whose immune systems are compromised, they can be immunosuppressive.

And from time to time, stories have surfaced about vaccines which have been dangerously contaminated, as a result of the manufacturing process.

We are taught to believe that untoward reactions to vaccines are rare, and that there has never been a question about the overwhelming success of all vaccines at all times, wherever they have been used.

The recent history of vaccines, though, shows a much more spotty record than one might think. In fact, it raises very disturbing questions about what vaccines do and don’t do to the human body. Here is simply a series of excerpts from several authors on the subject. It is a quite different slant on vaccines.

“The combined death rate from scarlet fever, diphtheria, whooping cough and measles among children up to fifteen shows that nearly 90 percent of the total decline in mortality between 1860 and 1965 had occurred before the introduction of antibiotics and widespread immunization. In part, this recession may be attributed to improved housing and to a decrease in the virulence of micro-organisms, but by far the most important factor was a higher host-resistance due to better nutrition.” Ivan Illich, Medical Nemesis, Bantam Books, 1977

“The principal evidence that… vaccines are effective actually dates from the more recent period, during which time the dreaded polio epidemics of the 1940s and 1950s have never reappeared in the developed countries; and measles, mumps and rubella, which even a generation ago were among the commonest diseases of childhood, have become far less prevalent, at least in their classic acute forms, since the triple MMR vaccine was introduced into common use.

“Yet how the vaccines actually accomplish these changes is not nearly as well understood as most people like to think it is. The disturbing possibility that they act in some other way than by producing a genuine immunity is suggested by the fact that the diseases in question have continued to break out even in highly immunized populations, and that in such cases the observed differences in incidence and severity between immunized and unimmunized persons have tended to be far less dramatic than expected, and in some cases, not measurably significant at all.

“In a recent British outbreak of whooping cough, for example, even fully immunized children contracted the disease in fairly large numbers; and the rates of serious complications and death were reduced only slightly. In another recent outbreak of pertussis, 46 of the 85 fully immunized children studied eventually contracted the disease.

“In 1977, 34 new cases of measles were reported on the campus of UCLA, in a population that was supposedly 91% immune, according to careful serological testing. Another 20 cases of measles were reported in the Pecos, New Mexico, area within a period of a few months in 1981, and 75% of them had been fully immunized, some of them quite recently. A survey of sixth-graders in a well-immunized urban community revealed that about 15% of this age group are still susceptible to rubella, a figure essentially identical with that of the pre-vaccine era.

“Finally, although the overall incidence of typical acute measles in the U.S. has dropped sharply from about 400,000 cases annually in the early 1960s to about 30,000 cases by 1974-76, the death rate remained exactly the same; and, with the peak incidence now occurring in adolescents and young adults, the risk of pneumonia and demonstrable liver abnormalities has actually increased substantially, according to one recent study, to well over 3% and 2%, respectively.” Richard Moskowitz, MD, The Case Against Immunizations, 1983, American Institute of Homeopathy.

“Of all reported whooping cough cases between 1979 and 1984 in children over 7 months of age – that is, old enough to have received the primary course of the DPT shots (diphtheria, pertussis, tetanus) – 41% occurred in children who had received three or more shots and 22% in children who had one or two immunizations.

“Among children under 7 months of age who had whooping cough, 34% had been immunized between one and three times…

“… Based on the only U.S. findings on adverse DPT reactions, an FDA-financed study at the University of California, Los Angeles, one out of every 350 children will have a convulsion; one in 180 children will experience high-pitched screaming; and one in 66 will have a fever of 105 degrees or more.” Jennifer Hyman, Democrat and Chronicle, Rochester, New York, special supplement on DPT, dated April, 1987.

“A study undertaken in 1979 at the University of California, Los Angeles, under the sponsorship of the Food and Drug Administration, and which has been confirmed by other studies, indicates that in the U.S.A. approximately 1,000 infants die annually as a direct result of DPT vaccinations, and these are classified as SIDS (Sudden Infant Death Syndrome) deaths. These represent about 10 to 15% of the total number of SIDS deaths occurring annually in the U.S.A. (between 8,000 and 10,000 depending on which statistics are used).” Leon Chaitow, Vaccination and Immunization, CW Daniel Company Limited, Saffron Walden, Essex, England, 1987.

“Assistant Secretary of Health Edward Brandt, Jr., MD, testifying before the U.S. Senate Committee on Labor and Human Resources, rounded… figures off to 9,000 cases of convulsions, 9,000 cases of collapse, and 17,000 cases of high-pitched screaming for a total of 35,000 acute neurological reactions occurring within forty-eight hours of a DPT shot among America’s children every year.” DPT: A Shot in the Dark, by Harris L. Coulter and Barbara Loe Fischer, Harcourt Brace Jovanovich.

“While 70-80% of British children were immunized against pertussis in 1970-71, the rate is now 39%. The committee predicts that the next pertussis epidemic will probably turn out to be more severe than the one in 1974/75. However, they do not explain why, in 1970/71, there were more than 33,000 cases of pertussis with 41 fatal cases among the very well immunized British child population; whereas in 1974/75, with a declining rate of vaccination, a pertussis epidemic caused only 25,000 cases with 25 fatalities.” Wolfgang Ehrengut, Lancet, Feb. 18, 1978, p. 370.

“… Barker and Pichichero, in a prospective study of 1232 children in Denver, Colorado, found after DTP that only 7% of those vaccinated were free from untoward reactions, which included pyrexia (53%), acute behavioral changes (82%), prolonged screaming (13%), and listlessness, anorexia and vomiting. 71% of those receiving second injections of DTP experienced two or more of the reactions monitored.” Lancet, May 28, 1983, p. 1217

“Publications by the World Health Organization show that diphtheria is steadily declining in most European countries, including those in which there has been no immunization. The decline began long before vaccination was developed. There is certainly no guarantee that vaccination will protect a child against the disease; in fact, over 30,000 cases of diphtheria have been recorded in the United Kingdom in fully immunized children.” Leon Chaitow, Vaccination and Immunization, p. 58.

“Pertussis (whooping cough) immunization is controversial, as the side effects have received a great deal of publicity. The counter claim is that the effectiveness and protection offered by the procedure far outweigh the possible ill effects… annual deaths, per million children, from this disease over the period from 1900 to the mid-nineteen seventies, shows that from a high point of just under 900 deaths per million children (under age 15) in 1905, the decline has been consistent and dramatic. There had been a lowering of mortality rates of approximately 80% by the time immunization was introduced on a mass scale, in the mid-nineteen fifties. The decline has continued, albeit at a slower rate, ever since. No credit can be given to vaccination for the major part of the decline since it was not in use.” Chaitow, Vaccination and Immunization, p. 63.

“… the swine-flu vaccination program was one of its (CDC) greatest blunders. It all began in 1976 when CDC scientists saw that a virus involved in a flu attack outbreak at Fort Dix, N.J., was similar to the swine-flu virus that killed 500,000 Americans in 1918. Health officials immediately launched a 100-million dollar program to immunize every American. But the expected epidemic never materialized, and the vaccine led to partial paralysis in 532 people. There were 32 deaths.” U.S. News and World Report, Joseph Carey, October 14, 1985, p. 70, “How Medical Sleuths Track Killer Diseases.”

“Despite (cases) in which (smallpox) vaccination plainly failed to protect the population, and despite the rampant side-effects of the methods, the proponents of vaccination continued their attempts to justify the methods by claims that the disease had declined in Europe as a whole during the period of its compulsory use. If the decline could be correlated with the use of the vaccination, then all else could be set aside, and the advantage between its current low incidence could be shown to outweigh the periodic failures of the method, and to favour the continued use of vaccination. However, the credit for the decline in the incidence of smallpox could not be given to vaccination. The fact is that its incidence declined in all parts of Europe, whether or not vaccination was employed.” Chaitow, Vaccination and Immunization, pp. 6-7.

“Smallpox, like typhus, has been dying out (in England) since 1780. Vaccination in this country has largely fallen into disuse since people began to realize how its value was discredited by the great smallpox epidemic of 1871-2 (which occurred after extensive vaccination).” W. Scott Webb, A Century of Vaccination, Swan Sonnenschein, 1898.

“In this incident (Kyoto, Japan, 1948) – the most serious of its kind – a toxic (vaccine) batch of alum-precipitated toxoid (APT) was responsible for illness in over 600 infants and for no fewer than 68 deaths.

“On 20 and 22 October, 1948, a large number of babies and children in the city of Kyoto received their first injection of APT. On the 4th and 5th of November, 15,561 babies and children aged some months to 13 years received their second dose. One to two days later, 606 of those who had been injected fell ill. Of these, 9 died of acute diphtheritic paralysis in seven to fourteen days, and 59 of late paralysis mainly in four to seven weeks.” Sir Graham Wilson, Hazards of Immunization, Athone Press, University of London, 1967.

“Accidents may, however, follow the use of this so-called killed (rabies) vaccine owing to inadequate processing. A very serious occurrence of this sort occurred at Fortaleza, Ceara, Brazil, in 1960. No fewer than 18 out of 66 persons vaccinated with Fermi’s carbolized (rabies) vaccine suffered from encephalomyelitis and every one of the eighteen died.” Sir Graham Wilson, Hazards of Immunization.

“At a press conference in Washington on 24 July, 1942, the Secretary of War reported that 28,585 cases of jaundice had been observed in the (American) Army between 1 January and 4 July after yellow fever vaccination, and of these 62 proved fatal.” Wilson, Hazards of Immunization.

“The world’s biggest trial (conducted in south India) to assess the value of BCG tuberculosis vaccine has made the startling revelation that the vaccine ‘does not give any protection against bacillary forms of tuberculosis.’ The study said to be ‘most exhaustive and meticulous,’ was launched in 1968 by the Indian Council of Medical Research (ICMR) with assistance from the World Health Organization (WHO) and the U.S. Centers for Disease Control in Atlanta, Georgia.

“The incidence of new cases among the BCG vaccinated group was slightly (but statistically insignificantly) higher than in the control group, a finding that led to the conclusion that BCG’s protective effect ‘was zero.'” New Scientist, November 15, 1979, as quoted by Hans Ruesch in Naked Empress, Civis Publishers, Switzerland, 1982.

“Between 10 December 1929 and 30 April 1930, 251 of 412 infants born in Lubeck received three doses of BCG vaccine by the mouth during the first ten days of life. Of these 251, 72 died of tuberculosis, most of them in two to five months and all but one before the end of the first year. In addition, 135 suffered from clinical tuberculosis but eventually recovered; and 44 became tuberculin-positive but remained well. None of the 161 unvaccinated infants born at the time was affected in this way and none of these died of tuberculosis within the following three years.” Hazards of Immunization, Wilson.

“We conducted a randomized double-blind placebo-controlled trial to test the efficacy of the 14-valent pneumococcal capsular polysaccharide vaccine in 2295 high-risk patients… Seventy-one episodes of proved or probable pneumococcal pneumonia or bronchitis occurred among 63 of the patients (27 placebo recipients and 36 vaccine recipients)… We were unable to demonstrate any efficacy of the pneumococcal vaccine in preventing pneumonia or bronchitis in this population.” New England Journal of Medicine, November 20, 1986, p. 1318, Michael Simberkoff et al.

In the spring of 1955, Cutter Labs started selling their standard polio vaccine. The vaccine was infective, and 200 cases of polio resulted among vaccinees. Of these, there were eleven deaths. About 100 cases of paralysis resulted. JR

“But already before Salk developed his vaccine, polio had been constantly regressing; the 39 cases out of every 100,000 inhabitants registered in 1942 had gradually diminished from year to year until they were reduced to only 15 cases in 1952… according to M. Beddow Baylay, the English surgeon and medical historian.” Slaughter of the Innocent, Hans Reusch, Civitas Publish ers, Switzerland, and Swain, New York, 1983.

“Many published stories and reports have stated, implied and otherwise led professional people and the public to believe that the sharp reduction of cases (and of deaths) from poliomyelitis in 1955 as compared to 1954 is attributable to the Salk vaccine… That it is a misconception follows from these considerations. The number of children inoculated has been too small to account for the decrease. The sharp decrease was apparent before the inoculations began or could take effect and was of the same order as the decrease following the immediate post-inoculation period.” Dr. Herbert Ratner, Child and Family, vol. 20, no. 1, 1987.

“So far it is hardly possible to gain insight into the extent of the immunization catastrophe of 1955 in the United States. It may be considered certain that the officially ascertained 200 cases (of polio) which were caused directly or indirectly by the (polio) vaccination constitute minimum figures… It can hardly be estimated how many of the 1359 (polio) cases among vaccinated persons must be regarded as failures of the vaccine and how many of them were infected by the vaccine. A careful study of the epidemiologic course of polio in the United States yields indications of grave significance. In numerous states of the U.S.A., typical early epidemics developed with the immunizations in the spring of 1955… The vaccination incidents of the year 1955 cannot be exclusively traced back to the failure of one manufacturing firm.” Dr. Herbert Ratner, Child and Family, 1980, vol. 19, no. 4, “Story of the Salk Vaccine (Part 2).”

“Suffice it to say that most of the large (polio) epidemics that have occurred in this country since the introduction of the Salk vaccine have followed the wide-scale use of the vaccine and have been characterized by an uncommon early seasonal onset. To name a few, there is the Massachusetts epidemic of 1955; the Chicago epidemic of 1956; and the Des Moines epidemic of 1959.” Dr. Herbert Ratner, Child and Family, 1980 vol. 19, no. 4.

“The live (Sabin) poliovirus vaccine has been the predominant cause of domestically arising cases of paralytic poliomyelitis in the United States since 1972. To avoid the occurrence of such cases, it would be necessary to discontinue the routine use of live poliovirus vaccine.” Jonas Salk, Science, March 4, 1977, p. 845.

“By the (U.S.) government’s own admission, there has been a 41% failure rate in persons who were previously vaccinated against the (measles) virus.” Dr. Anthony Morris, John Chriss, BG Young, “Occurrence of Measles in Previously Vaccinated Individuals,” 1979; presented at a meeting of the American Society for Microbiology at Fort Detrick, Maryland, April 27, 1979.

“Prior to the time doctors began giving rubella (measles) vaccinations, an estimated 85% of adults were naturally immune to the disease (for life). Because of immunization, the vast majority of women never acquire natural immunity (or lifetime protection).” Dr. Robert Mendelsohn, Let’s Live, December 1983, as quoted by Carolyn Reuben in the LA WEEKLY, June 28, 1985.

“Adminstration of KMV (killed measles vaccine) apparently set in motion an aberrant immunologic response that not only failed to protect children against natural measles, but resulted in heightened susceptibility.” JAMA Aug. 22, 1980, vol. 244, p. 804, Vincent Fulginiti and Ray Helfer. The authors indicate that such falsely protected children can come down with “an often severe, atypical form of measles. Atypical measles is characterized by fever, headache… and a diverse rash (which)… may consist of a mixture of macules, papules, vesicles, and pustules… ”

The above quotes reflect only a mere fraction of an available literature which shows there is a need for an extensive review of vaccination. It is certain that undisclosed, unlooked for illness occurs as a result of vaccines. A certain amount of this sort of illness is immunosuppressive in the widest sense, and some in a narrower sense (depression of T-cell numbers, etc.). When looking for unusual illness and immune depression, vaccines are one of those areas which remain partially hidden from investigation. That is a mistake. It is not adequate to say, “Vaccines are simple; they stimulate the immune system and confer immunity against specific germ agents.” That is the glossy presentation. What vaccines apparently often do is something else. They engage some aspect of the body’s immune-response, but to what effect over the long term? Why, for example, do children who have measles vaccine develop a susceptibility to another more severe, atypical measles?

Official reports on vaccine reactions are often at odds with unofficial estimates because of the method of analysis used. If vaccine-reaction is defined as a small set of possible effects experienced within 72 hours of an inoculation, then figures will be smaller. But doctors like G.T. Stewart, of the University of Glasgow, have found through meticulous investigation, including visits to hospitals and interviews with parents of vaccinated children, that reactions as severe as brain-damage (e.g., from the DPT vaccine) can be overlooked, go unreported and can be assumed mistakenly to have come from other causes.

—end of 1987-8 chapter—

These days, my comments on the destructive effects of vaccines and their completely needless use are much more aggressive, owing to further research, and discoveries about so-called “viruses,” the great fairy tales that rank with the green cheese of the moon.


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(To read about Jon’s mega-collection, The Matrix Revealed, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

Now: Stop FDA authorization of COVID shot for kids

Stand at the gates of Hell

by Jon Rappoport

March 31, 2022

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A faceless Nazi bureaucracy is poised, waiting for the FDA’s signal to advance on small children and infants, with needles of death.

You can find all the government contact info and talking points — as well as the entire time line of developments, here, here, here, and here — in Toby Rogers’ articles. Also read this stunning article by Celia Farber.

And then raise the Alarm on all fronts. Raise holy hell.

The FDA is taking another run at authorizing the horrific COVID vaccine for children, ages 6 months to 4 years. This is murder and maiming right out in the open.

Even from a conventional medical position, it’s senseless: It’s trying to prevent a disease that doesn’t happen in children. It’s straight-out slaughter.

The federal database contains well over a million reports of injuries from the COVID vaccine. And that figure represents vast UNDER-reporting.

The medical apparatus that administers these shots is remorseless. It doesn’t think. It just acts under orders. It doesn’t stop and wonder about the little children and infants. It has no conscience. It doesn’t need to explain itself. It only has to say, “The vaccine was authorized.”

And the body that authorizes it only has to say, “We weighed the benefits against the risks, and came to the conclusion we did.”

And then the new death march begins.

Evidence for the FDA’s decision? There is no evidence. There is only cooked data and hidden data. There is only the FDA hand in glove with Pfizer and Moderna. Partners.

There is only money and greed and control and destruction of life.

The slaughter of the innocents.

Do what they’ve been telling you to do: see something, say something.

THEY are the insurrectionists. THEY are the terrorists.


The Matrix Revealed

(To read about Jon’s mega-collection, The Matrix Revealed, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

Real war vs. phony war; turn on the news bubble machine

by Jon Rappoport

March 2, 2022

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“The CIA infiltrated the media.” That statement wore out its welcome decades ago. The media ARE the CIA.

The only proviso, if you want to call it that: most reporters are too stupid to realize who they slave for.

I mention this because we’re not getting war news, we’re getting CIA news.

Now on the other hand, here is a WRITER—I don’t know who he is; his handle is Good Citizen on Substack. I’ll tell you this. If I could, I’d appoint him to head up negotiations between Russia and the Ukraine in a New York minute. Screw in your brain tightly and read what he recently laid down in one of his carpet bombing runs:

“Imagine this scenario of aggression. Russia has established something called SATA. (Surround America Together Alliance) with the Bahamas, Cuba, Canada and all of Central America. Article 5 of SATA says if one goes to war, they all go to war. Putin is trying to get Mexico to join. He orchestrated a coup there in 2014 and installed a puppet dictator who helps enrich Putin through Putin’s crack head son. He keeps assuring Mexico they will join SATA one day, even though the other countries would not approve the vote and they don’t meet some minimum requirements. Other politicians in the duma send their kids to be on boards of Mexican companies to collect paychecks of $50,000 per month. Russia keeps sending weapons to Mexico who has a neo-Nazi force of nationalists near the border who take shots at English speaking American separatists who would prefer to be part of the United States. Cease fires are broken 2000 times over 8 years, leaving 14,000 dead in the conflict. The U.S. has taken a patient stance, trying to reason with the Mexican coke-head dictator but he keeps accepting SATA weapons and money. Last week the Mexican dictator said he doesn’t just want SATA membership, he wants Russian nukes in his country aimed at the United States. That was the final straw. Tuesday the U.S. launched air strikes across Mexico and declared those English speaking American states as independent republics.”

It’s hard for Americans to consider that they’re living in a news bubble cut off from reality. That grisly fate is supposed to befall lesser countries.

And when American news involves foreign policy, the bubble is double, because that’s where American oligarchs have traditionally stolen a great deal of their money, and “don’t tell the children” has always been the motto of the CIA.

For readers who’ve been following my 2-year assault on the medical bubble surrounding the non-pandemic called COVID, think of the CIA as the CDC of political criminality. The CIA locks down countries. They “vaccinate countries and improve their immunity” by staging coups. They tell you which countries are viruses. They “stop the spread.”

We only see the least clever CIA people delivering the news on television, because those anchors have to be dumb; they have to believe they’re dispensing truth. They have to be unaware that cover stories, limited hangouts, false trails, appeals to authority, and straw man arguments are the stock-in-trade of standard intelligence operations.

If you told anchors Lester “Lurch” Holt or David “Sears underwear model” Muir that the puppet-comedian President of the Ukraine was handing out thousands of weapons to ordinary untrained citizens with the inevitable effect of many of them dying—for television coverage—Lester and David would have no idea what you were talking about.

Here’s a CIA-CDC parallel. The first great signal that the CIA had captured American news came in the wake of the JFK assassination—when US media unanimously agreed the Warren Commission had the facts straight: Oswald acted alone. This, despite nagging evidence (which piled up in future years) that the CIA itself had engineered the President’s murder.

In 1986, in a notorious deal between the US Congress and vaccine manufacturers, a law was passed which ruled out a citizen suing a manufacturer for toxic vaccine damage. Instead, the plaintiff had to appeal to a Kafka-esque federal “court” for compensation. At that point, the truth began to dawn. The CDC was in the big business of buying and selling vaccines; it was also in charge of reporting statistics on vaccine damage; and it was also conducting studies to assess vaccine safety and efficacy. News media took no notice of any of these facts—which when you added them up, amounted to mass murder by vaxx.

Two giant news bubbles, inside which the American population lived. Unaware.

Just as the CIA travels to distant lands, subverts and topples governments, paves the way for mega-corporate takeovers, and then feeds fantasies back to news networks, the medical CIA—the CDC—has it own crew of invaders. They’re called the Epidemic Intelligence Service (EIS).

These trained medical personnel carry out several hundred missions a year, to foreign lands where possible “outbreaks” are occurring.

They are the virus hunters. They’ve never met a non-existent virus they didn’t love.

Graduates of this EIS program, as proudly stated by the CDC, have gone on to occupy key positions in the overall medical cartel: Surgeons General; CDC directors; medical school deans and professors; medical foundation executives; drug-company and insurance executives; state health officials; MEDICAL EDITORS AND REPORTERS IN MEDIA OUTLETS. —Power, at key junctures.

It’s a loyal insider’s club. They collaborate to float prime-cut, A-number-one cover stories of extraordinary dimensions. They invent reality out of thin air.

They front for the medical cartel. And they provide cover for the crimes of mega-corporations. There’s a foreign town where poverty-stricken people are dying, because horrendous pesticides are running into the soil? No, it’s a virus. There’s a city where the industrial pollution is driving people over the edge into immune-system failure? No, it’s a virus. Dead fish are floating on a yellow and purple river next to a factory pipe that’s pouring steaming poison into the water? No, it’s a new virus no one knew existed.

And here’s the capper. Their propaganda is so good most of the EIS people (just like the news anchors) believe it themselves. You don’t achieve that kind of robotic servitude without intense brainwashing. The first installment of the mind-control program is called medical school.

The EIS would have you imagine the whole world is being attacked by viruses, all the time. That’s their mission.

Bubbles.

News bubbles.

War news bubbles.

Medical and pandemic news bubbles.

Try one on for size.

Walk inside one and live there.

Nothing to lose, except your mind.

And everything that follows from that.


The Matrix Revealed

(To read about Jon’s mega-collection, The Matrix Revealed, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

FDA ready to OK the vaxx for babies; why not just throw the babies off a cliff into a volcano?

by Jon Rappoport

February 11, 2022

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And the answer to that question is obvious. Throwing babies into a volcano makes no money for Pfizer.

On Feb. 15, the FDA will decide whether to approve the Pfizer COVID shot for children between the ages of six months and four years. The press and gov’t. spokespeople predict it’s a GO.

This is murder.

The FDA approval committee members will come in several categories: those who’ve been paid off; those who’ve been threatened; straight-out cold Nazi bureaucrats; those who’ve been blackmailed; and those who WANT TO murder babies.

You can’t get around this. Given the mainstream view of COVID, these FDA/CDC people KNOW the risk of the disease to babies is non-existent, and risks of the vaccine are absolutely devastating.

—Over a million vaccine injuries have already been reported to the US federal database; and this number represents vast UNDER-REPORTING.

Nevertheless, the FDA deciders are ready to say, unless exposed for what they are: inject the babies; kill the babies.

If you still think the government COVID response had anything to do with science or public health or human concern, if you’re still making excuses for Fauci and the whole rogue crew of predators and maniacs at the FDA and CDC, you’re an automatic robot; you just don’t know it.

Get a load of this. CNBC: “Pfizer amended its clinical trial in December to evaluate a third dose after two shots did not induce an adequate immune response in children 2- to 4-years-old. Pfizer and BioNTech said they will submit data on the third dose to the FDA in the coming months.”

I see. The vaccine didn’t work after 2 shots, but it’ll be approved anyway in few days, and Pfizer will let us know IN A FEW MONTHS how the third shot worked.

And that’s science. That’s the bullshit the educated class believes in. That’s the bullshit the deaf, dumb, and blind believe in.

And THE TRUCKERS are the terrorists. Sure. The government is righteous and just. Of course.

People “who spread misinformation about COVID” are terrorists. The government is righteous and just.

Love the government. Hate the terrorists.

Memo to parents: if you’ve been crazy enough to take the shots yourselves, are you ready to deliver your innocent babies into the hands of doctors and nurses who’ll spin the roulette wheel of death and inject their bodies? Is that what you’re going to do?

If so, why? Do you think it’ll make a nice talking point when you get together with friends? Do you think it’s a potent virtue signal? Do you think it proves you’re a loyal subject of the king?

Perhaps you can show up at a local school board meeting, with your infant in your arms; and you can look at the doughy morbid faces of the low-rent grifters sitting behind their long table, and you can say, “Look! I just had my baby shot with the vaccine! It’s wonderful!” And they’ll nod approvingly.

And some piece of dreck who picks up a paycheck as a city public health official will speak at the meeting. He might say vaccinated babies should wear masks. Ask him and find out. Look at his eyes. His brother-in-law, who knows the mayor, rescued him from a career as a gravedigger.

I want to know what the Pope thinks. He’s already stated taking the vaccine is a loving gift to God. What about the babies? Does Popius Maximus Jesuiticus believe The Lord wants infants injected? Let’s get this Pontiff on the record.

Would Mary, in her hut, have told the local doc to inject baby Jesus? Perhaps her husband Joseph, a minor character in the story up to that point, would have brandished a Glock and motioned the sawbones to the door.

Speaking of guns, I think four or five Secret Service agents, their weapons drawn, should usher Nurse Jill to the White House residence, where she will speak candidly and starkly to old Joe—spending as much time as necessary informing him about what the FDA is ready to do, until he UNDERSTANDS.

Then, the agents will force Joe in front of a camera—going live on major channels—where he will unambiguously declare his position on injecting babies.

If he supports the program, he will take full responsibility for the consequences.

After all, the FDA is an agency in the Executive Branch, under the President.

The buck stops with him. It should stop under harsh television spotlights, where no tap-dancing is permitted.

Of course, you parents will have the last word. Unless the guns of the State are pointed at you. If that comes to pass, are you ready to die fighting for your children?

Or will you sacrifice them on the altar of your own passivity and cowardice?

I STRONGLY suggest you make your position clear now.

Publically.

Leave no doubt.

Before it’s too late.

WE NEED AN UPROAR.

Are you standing up? Or are you grinning and virtue signaling—down on your knees?


The Matrix Revealed

(To read about Jon’s mega-collection, The Matrix Revealed, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

Pfizer smoking-gun secret document: their deadly COVID vaccine

Awakening from the trance

by Jon Rappoport

December 7, 2021

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CORRECTION: After publishing this article, I discovered that the gigantic Pfizer list of medical conditions was apparently not a report on logged cases of adverse events, but instead a complete list of conditions that Pfizer would be monitoring, in order to see whether they popped up on their radar as reactions to the COVID vaccine.

Why would Pfizer publish this extraordinary list? Because as they state, these medical conditions have been associated with severe COVID-19 “and vaccines in general.” In other words, vaccines in general, historically, have carried enormous risk and dangers over an incredibly wide area of medical conditions. This is a key confession.

Further, if you read the full secret Pfizer document, you will come to Table 7, which does list a number of categories of adverse reactions, all of which WERE reported in the first three months of the Pfizer vaccine rollout. This IS stunning.

In the secret document, Pfizer does list 1,223 deaths occurring after just three months of the vaccine rollout. This should have been sufficient to cause a complete halt to the vaccination program.

Finally, Pfizer admits that in the first three months of the vaccine rollout, it logged a staggering 42,086 cases of adverse reactions. And as far as I can determine from the Pfizer document, these 42,086 cases represented a total of 139,888 adverse events. In other words, in many cases, there were reports of multiple adverse events.


Journalist Celia Farber just wrote an explosive article on the Pfizer secret document. You should read it (and her addendum, here). She deserves our thanks and gratitude. And here you can also read the document itself.

In short, the Pfizer document (which was never supposed to see the light of day but was disclosed as part of a FOIA suit) describes the adverse effects from just the first three months of injections with the company’s COVID vaccine:

158,000 adverse events, 1,223 deaths. In a half-sane world, this would have been more than enough to halt all injections and cancel the vaccine.

I’ve queried two attorneys. They both looked at the Pfizer document and state they believe it’s authentic.

The appendix of the Pfizer document is the most astonishing section. It’s beyond astonishing. It lists all the types of vaccine adverse events Pfizer logged—again, in just three months of injections.

Page after page after page after page of types of adverse events. Each type of event cast in medical language, the language of the dead. The proponents of this technical-ese speak, as it were, from beyond the grave. They’re super-educated brainwashed zombies. It’s as if they’re listing and counting abstractions in an academic board game.

The abstractions raise no concerns. In the document, no one is waving red flags. They’re all medical bean counters, keeping their books with precision.

Make no mistake, these are the people who are operating the levers of society on a day-to-day basis, maiming and killing with a confident attitude that indicates they are beyond reproach. The very notion of reproach is foreign to them.

Civilization is drowning. It’s drowning in a giant lake of TECHNIQUE. The uses to which technique is put have become irrelevant. Just follow procedure. Carry out assigned tasks. Pass along information. Report on results. And then you will have achieved immunity from blame.

Or resist and rebel no matter what. These are the stakes. This is the war.

Get ready. Buckle up. Logged by Pfizer, covering the first three months of COVID vaccination, here is the corporation’s list of types of vaccine adverse events, as published by Celia Farber:


BNT162b2

5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

APPENDIX 1. LIST OF ADVERSE EVENTS OF SPECIAL INTEREST

1p36 deletion syndrome; 2-Hydroxyglutaric aciduria; 5’nucleotidase increased; Acoustic neuritis; Acquired C1 inhibitor deficiency; Acquired epidermolysis bullosa; Acquired epileptic aphasia; Acute cutaneous lupus erythematosus; Acute disseminated encephalomyelitis; Acute encephalitis with refractory, repetitive partial seizures; Acute febrile neutrophilic dermatosis; Acute flaccid myelitis; Acute haemorrhagic leukoencephalitis; Acute haemorrhagic oedema of infancy; Acute kidney injury; Acute macular outer retinopathy; Acute motor axonal neuropathy; Acute motor-sensory axonal neuropathy; Acute myocardial infarction; Acute respiratory distress syndrome [Note by Celia Farber: “that sounds like ‘Covid 19’.”]; Acute respiratory failure; Addison’s disease; Administration site thrombosis; Administration site vasculitis; Adrenal thrombosis; Adverse event following immunisation; Ageusia; Agranulocytosis; Air embolism; Alanine aminotransferase abnormal; Alanine aminotransferase increased; Alcoholic seizure; Allergic bronchopulmonary mycosis; Allergic oedema; Alloimmune hepatitis; Alopecia areata; Alpers disease; Alveolar proteinosis; Ammonia abnormal; Ammonia increased; Amniotic cavity infection; Amygdalohippocampectomy; Amyloid arthropathy; Amyloidosis; Amyloidosis senile; Anaphylactic reaction; Anaphylactic shock; Anaphylactic transfusion reaction; Anaphylactoid reaction; Anaphylactoid shock; Anaphylactoid syndrome of pregnancy; Angioedema; Angiopathic neuropathy; Ankylosing spondylitis; Anosmia; Antiacetylcholine receptor antibody positive; Anti-actin antibody positive; Anti-aquaporin-4 antibody positive; Anti-basal ganglia antibody positive; Anti-cyclic citrullinated peptide antibody positive; Anti-epithelial antibody positive; Anti-erythrocyte antibody positive; Anti-exosome complex antibody positive; Anti- GAD antibody negative; Anti-GAD antibody positive; Anti-ganglioside antibody positive; Antigliadin antibody positive; Anti-glomerular basement membrane antibody positive; Anti-glomerular basement membrane disease; Anti-glycyl-tRNA synthetase antibody positive; Anti-HLA antibody test positive; Anti-IA2 antibody positive; Anti-insulin antibody increased; Anti-insulin antibody positive; Anti-insulin receptor antibody increased; Anti-insulin receptor antibody positive; Anti-interferon antibody negative; Anti-interferon antibody positive; Anti-islet cell antibody positive; Antimitochondrial antibody positive; Anti-muscle specific kinase antibody positive; Anti-myelin-associated glycoprotein antibodies positive; Anti-myelin-associated glycoprotein associated polyneuropathy; Antimyocardial antibody positive; Anti-neuronal antibody positive; Antineutrophil cytoplasmic antibody increased; Antineutrophil cytoplasmic antibody positive; Anti-neutrophil cytoplasmic antibody positive vasculitis; Anti-NMDA antibody positive; Antinuclear antibody increased; Antinuclear antibody positive; Antiphospholipid antibodies positive; Antiphospholipid syndrome; Anti-platelet antibody positive; Anti-prothrombin antibody positive; Antiribosomal P antibody positive; Anti-RNA polymerase III antibody positive; Anti-saccharomyces cerevisiae antibody test positive; Anti-sperm antibody positive; Anti-SRP antibody positive; Antisynthetase syndrome; Anti-thyroid antibody positive; Anti-transglutaminase antibody increased; Anti-VGCC antibody positive; Anti-VGKC antibody positive; Anti-vimentin antibody positive; Antiviral prophylaxis; Antiviral treatment; Anti-zinc transporter 8 antibody positive; Aortic embolus; Aortic thrombosis; Aortitis; Aplasia pure red cell; Aplastic anaemia; Application site thrombosis; Application site vasculitis; Arrhythmia; Arterial bypass occlusion; Arterial bypass thrombosis; Arterial thrombosis; Arteriovenous fistula thrombosis; Arteriovenous graft site stenosis; Arteriovenous graft thrombosis; Arteritis; Arteritis

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5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

[con’t] [Arteritis] coronary; Arthralgia; Arthritis; Arthritis enteropathic; Ascites; Aseptic cavernous sinus thrombosis; Aspartate aminotransferase abnormal; Aspartate aminotransferase increased; Aspartate-glutamate-transporter deficiency; AST to platelet ratio index increased; AST/ALT ratio abnormal; Asthma; Asymptomatic COVID-19; Ataxia; Atheroembolism; Atonic seizures; Atrial thrombosis; Atrophic thyroiditis; Atypical benign partial epilepsy; Atypical pneumonia [Note by Celia Farber: “This sounds like the original definition of Covid-19 out of Wuhan.”]; Aura; Autoantibody positive; Autoimmune anaemia; Autoimmune aplastic anaemia; Autoimmune arthritis; Autoimmune blistering disease; Autoimmune cholangitis; Autoimmune colitis; Autoimmune demyelinating disease; Autoimmune dermatitis; Autoimmune disorder; Autoimmune encephalopathy; Autoimmune endocrine disorder; Autoimmune enteropathy; Autoimmune eye disorder; Autoimmune haemolytic anaemia; Autoimmune heparin-induced thrombocytopenia; Autoimmune hepatitis; Autoimmune hyperlipidaemia; Autoimmune hypothyroidism; Autoimmune inner ear disease; Autoimmune lung disease; Autoimmune lymphoproliferative syndrome; Autoimmune myocarditis; Autoimmune myositis; Autoimmune nephritis; Autoimmune neuropathy; Autoimmune neutropenia; Autoimmune pancreatitis; Autoimmune pancytopenia; Autoimmune pericarditis; Autoimmune retinopathy; Autoimmune thyroid disorder; Autoimmune thyroiditis; Autoimmune uveitis; Autoinflammation with infantile enterocolitis; Autoinflammatory disease; Automatism epileptic; Autonomic nervous system imbalance; Autonomic seizure; Axial spondyloarthritis; Axillary vein thrombosis; Axonal and demyelinating polyneuropathy; Axonal neuropathy; Bacterascites; Baltic myoclonic epilepsy; Band sensation; Basedow’s disease; Basilar artery thrombosis; Basophilopenia; B-cell aplasia; Behcet’s syndrome; Benign ethnic neutropenia; Benign familial neonatal convulsions; Benign familial pemphigus; Benign rolandic epilepsy; Beta-2 glycoprotein antibody positive; Bickerstaff’s encephalitis; Bile output abnormal; Bile output decreased; Biliary ascites; Bilirubin conjugated abnormal; Bilirubin conjugated increased; Bilirubin urine present; Biopsy liver abnormal; Biotinidase deficiency; Birdshot chorioretinopathy; Blood alkaline phosphatase abnormal; Blood alkaline phosphatase increased; Blood bilirubin abnormal; Blood bilirubin increased; Blood bilirubin unconjugated increased; Blood cholinesterase abnormal; Blood cholinesterase decreased; Blood pressure decreased; Blood pressure diastolic decreased; Blood pressure systolic decreased; Blue toe syndrome; Brachiocephalic vein thrombosis; Brain stem embolism; Brain stem thrombosis; Bromosulphthalein test abnormal; Bronchial oedema; Bronchitis; Bronchitis mycoplasmal; Bronchitis viral; Bronchopulmonary aspergillosis allergic; Bronchospasm; Budd- Chiari syndrome; Bulbar palsy; Butterfly rash; C1q nephropathy; Caesarean section; Calcium embolism; Capillaritis; Caplan’s syndrome; Cardiac amyloidosis; Cardiac arrest; Cardiac failure; Cardiac failure acute; Cardiac sarcoidosis; Cardiac ventricular thrombosis; Cardiogenic shock; Cardiolipin antibody positive; Cardiopulmonary failure; Cardio-respiratory arrest; Cardio-respiratory distress; Cardiovascular insufficiency; Carotid arterial embolus; Carotid artery thrombosis; Cataplexy; Catheter site thrombosis; Catheter site vasculitis; Cavernous sinus thrombosis; CDKL5 deficiency disorder; CEC syndrome; Cement embolism; Central nervous system lupus; Central nervous system vasculitis; Cerebellar artery thrombosis; Cerebellar embolism; Cerebral amyloid angiopathy; Cerebral arteritis; Cerebral artery embolism; Cerebral artery thrombosis; Cerebral gas embolism; Cerebral microembolism; Cerebral septic infarct; Cerebral thrombosis; Cerebral venous sinus thrombosis; Cerebral venous thrombosis; Cerebrospinal thrombotic

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BNT162b2

5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

[con’t] [Cerebrospinal thrombotic] tamponade; Cerebrovascular accident; Change in seizure presentation; Chest discomfort; Child- Pugh-Turcotte score abnormal; Child-Pugh-Turcotte score increased; Chillblains; Choking; Choking sensation; Cholangitis sclerosing; Chronic autoimmune glomerulonephritis; Chronic cutaneous lupus erythematosus; Chronic fatigue syndrome; Chronic gastritis; Chronic inflammatory demyelinating polyradiculoneuropathy; Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids; Chronic recurrent multifocal osteomyelitis; Chronic respiratory failure; Chronic spontaneous urticaria; Circulatory collapse; Circumoral oedema; Circumoral swelling; Clinically isolated syndrome; Clonic convulsion; Coeliac disease; Cogan’s syndrome; Cold agglutinins positive; Cold type haemolytic anaemia; Colitis; Colitis erosive; Colitis herpes; Colitis microscopic; Colitis ulcerative; Collagen disorder; Collagen-vascular disease; Complement factor abnormal; Complement factor C1 decreased; Complement factor C2 decreased; Complement factor C3 decreased; Complement factor C4 decreased; Complement factor decreased; Computerised tomogram liver abnormal; Concentric sclerosis; Congenital anomaly; Congenital bilateral perisylvian syndrome; Congenital herpes simplex infection; Congenital myasthenic syndrome; Congenital varicella infection; Congestive hepatopathy; Convulsion in childhood; Convulsions local; Convulsive threshold lowered; Coombs positive haemolytic anaemia; Coronary artery disease; Coronary artery embolism; Coronary artery thrombosis; Coronary bypass thrombosis; Coronavirus infection; Coronavirus test; Coronavirus test negative; Coronavirus test positive; Corpus callosotomy; Cough; Cough variant asthma; COVID-19; COVID-19 immunisation; COVID-19 pneumonia; COVID-19 prophylaxis; COVID-19 treatment; Cranial nerve disorder; Cranial nerve palsies multiple; Cranial nerve paralysis; CREST syndrome; Crohn’s disease; Cryofibrinogenaemia; Cryoglobulinaemia; CSF oligoclonal band present; CSWS syndrome; Cutaneous amyloidosis; Cutaneous lupus erythematosus; Cutaneous sarcoidosis; Cutaneous vasculitis; Cyanosis; Cyclic neutropenia; Cystitis interstitial; Cytokine release syndrome; Cytokine storm; De novo purine synthesis inhibitors associated acute inflammatory syndrome; Death neonatal; Deep vein thrombosis; Deep vein thrombosis postoperative; Deficiency of bile secretion; Deja vu; Demyelinating polyneuropathy; Demyelination; Dermatitis; Dermatitis bullous; Dermatitis herpetiformis; Dermatomyositis; Device embolisation; Device related thrombosis; Diabetes mellitus; Diabetic ketoacidosis; Diabetic mastopathy; Dialysis amyloidosis; Dialysis membrane reaction; Diastolic hypotension; Diffuse vasculitis; Digital pitting scar; Disseminated intravascular coagulation; Disseminated intravascular coagulation in newborn; Disseminated neonatal herpes simplex; Disseminated varicella; Disseminated varicella zoster vaccine virus infection; Disseminated varicella zoster virus infection; DNA antibody positive; Double cortex syndrome; Double stranded DNA antibody positive; Dreamy state; Dressler’s syndrome; Drop attacks; Drug withdrawal convulsions; Dyspnoea; Early infantile epileptic encephalopathy with burst-suppression; Eclampsia; Eczema herpeticum; Embolia cutis medicamentosa; Embolic cerebellar infarction; Embolic cerebral infarction; Embolic pneumonia; Embolic stroke; Embolism; Embolism arterial; Embolism venous; Encephalitis; Encephalitis allergic; Encephalitis autoimmune; Encephalitis brain stem; Encephalitis haemorrhagic; Encephalitis periaxialis diffusa; Encephalitis post immunisation; Encephalomyelitis; Encephalopathy; Endocrine disorder; Endocrine ophthalmopathy; Endotracheal intubation; Enteritis; Enteritis leukopenic; Enterobacter pneumonia; Enterocolitis; Enteropathic spondylitis; Eosinopenia; Eosinophilic

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5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

[con’t] [Eosinophilic] fasciitis; Eosinophilic granulomatosis with polyangiitis; Eosinophilic oesophagitis; Epidermolysis; Epilepsy; Epilepsy surgery; Epilepsy with myoclonic-atonic seizures; Epileptic aura; Epileptic psychosis; Erythema; Erythema induratum; Erythema multiforme; Erythema nodosum; Evans syndrome; Exanthema subitum; Expanded disability status scale score decreased; Expanded disability status scale score increased; Exposure to communicable disease; Exposure to SARS-CoV-2; Eye oedema; Eye pruritus; Eye swelling; Eyelid oedema; Face oedema; Facial paralysis; Facial paresis; Faciobrachial dystonic seizure; Fat embolism; Febrile convulsion; Febrile infection-related epilepsy syndrome; Febrile neutropenia; Felty’s syndrome; Femoral artery embolism; Fibrillary glomerulonephritis; Fibromyalgia; Flushing; Foaming at mouth; Focal cortical resection; Focal dyscognitive seizures; Foetal distress syndrome; Foetal placental thrombosis; Foetor hepaticus; Foreign body embolism; Frontal lobe epilepsy; Fulminant type 1 diabetes mellitus; Galactose elimination capacity test abnormal; Galactose elimination capacity test decreased; Gamma-glutamyltransferase abnormal; Gamma-glutamyltransferase increased; Gastritis herpes; Gastrointestinal amyloidosis; Gelastic seizure; Generalised onset non-motor seizure; Generalised tonic-clonic seizure; Genital herpes; Genital herpes simplex; Genital herpes zoster; Giant cell arteritis; Glomerulonephritis; Glomerulonephritis membranoproliferative; Glomerulonephritis membranous; Glomerulonephritis rapidly progressive; Glossopharyngeal nerve paralysis; Glucose transporter type 1 deficiency syndrome; Glutamate dehydrogenase increased; Glycocholic acid increased; GM2 gangliosidosis; Goodpasture’s syndrome; Graft thrombosis; Granulocytopenia; Granulocytopenia neonatal; Granulomatosis with polyangiitis; Granulomatous dermatitis; Grey matter heterotopia; Guanase increased; Guillain- Barre syndrome; Haemolytic anaemia; Haemophagocytic lymphohistiocytosis; Haemorrhage; Haemorrhagic ascites; Haemorrhagic disorder; Haemorrhagic pneumonia; Haemorrhagic varicella syndrome; Haemorrhagic vasculitis; Hantavirus pulmonary infection; Hashimoto’s encephalopathy; Hashitoxicosis; Hemimegalencephaly; Henoch-Schonlein purpura; Henoch- Schonlein purpura nephritis; Hepaplastin abnormal; Hepaplastin decreased; Heparin-induced thrombocytopenia; Hepatic amyloidosis; Hepatic artery embolism; Hepatic artery flow decreased; Hepatic artery thrombosis; Hepatic enzyme abnormal; Hepatic enzyme decreased; Hepatic enzyme increased; Hepatic fibrosis marker abnormal; Hepatic fibrosis marker increased; Hepatic function abnormal; Hepatic hydrothorax; Hepatic hypertrophy; Hepatic hypoperfusion; Hepatic lymphocytic infiltration; Hepatic mass; Hepatic pain; Hepatic sequestration; Hepatic vascular resistance increased; Hepatic vascular thrombosis; Hepatic vein embolism; Hepatic vein thrombosis; Hepatic venous pressure gradient abnormal; Hepatic venous pressure gradient increased; Hepatitis; Hepatobiliary scan abnormal; Hepatomegaly; Hepatosplenomegaly; Hereditary angioedema with C1 esterase inhibitor deficiency; Herpes dermatitis; Herpes gestationis; Herpes oesophagitis; Herpes ophthalmic; Herpes pharyngitis; Herpes sepsis; Herpes simplex; Herpes simplex cervicitis; Herpes simplex colitis; Herpes simplex encephalitis; Herpes simplex gastritis; Herpes simplex hepatitis; Herpes simplex meningitis; Herpes simplex meningoencephalitis; Herpes simplex meningomyelitis; Herpes simplex necrotising retinopathy; Herpes simplex oesophagitis; Herpes simplex otitis externa; Herpes simplex pharyngitis; Herpes simplex pneumonia; Herpes simplex reactivation; Herpes simplex sepsis; Herpes simplex viraemia; Herpes simplex virus conjunctivitis neonatal; Herpes simplex visceral; Herpes virus

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[con’t] [Herpes virus] infection; Herpes zoster; Herpes zoster cutaneous disseminated; Herpes zoster infection neurological; Herpes zoster meningitis; Herpes zoster meningoencephalitis; Herpes zoster meningomyelitis; Herpes zoster meningoradiculitis; Herpes zoster necrotising retinopathy; Herpes zoster oticus; Herpes zoster pharyngitis; Herpes zoster reactivation; Herpetic radiculopathy; Histone antibody positive; Hoigne’s syndrome; Human herpesvirus 6 encephalitis; Human herpesvirus 6 infection; Human herpesvirus 6 infection reactivation; Human herpesvirus 7 infection; Human herpesvirus 8 infection; Hyperammonaemia; Hyperbilirubinaemia; Hypercholia; Hypergammaglobulinaemia benign monoclonal; Hyperglycaemic seizure; Hypersensitivity; Hypersensitivity vasculitis; Hyperthyroidism; Hypertransaminasaemia; Hyperventilation; Hypoalbuminaemia; H ypocalcaemic seizure; Hypogammaglobulinaemia; Hypoglossal nerve paralysis; Hypoglossal nerve paresis; Hypoglycaemic seizure; Hyponatraemic seizure; Hypotension; Hypotensive crisis; Hypothenar hammer syndrome; Hypothyroidism; Hypoxia; Idiopathic CD4 lymphocytopenia [Note by Celia Farber: “sounds like ‘AIDS’ except Fauci re-defined AIDS in 1993, after the ‘Amsterdam Surprise’ as only occurring when HIV was ‘present’ so all thousands the non HIV, ‘idiopathic CD4 lympho-cytopenia’ cases were excluded, creating a tautological definition that came to be ‘HIV/AIDS’.”]; Idiopathic generalised epilepsy; Idiopathic interstitial pneumonia; Idiopathic neutropenia; Idiopathic pulmonary fibrosis; IgA nephropathy; IgM nephropathy; IIIrd nerve paralysis; IIIrd nerve paresis; Iliac artery embolism; Immune thrombocytopenia; Immune- mediated adverse reaction; Immune-mediated cholangitis; Immune-mediated cholestasis; Immune-mediated cytopenia; Immune-mediated encephalitis; Immune-mediated encephalopathy; Immune-mediated endocrinopathy; Immune-mediated enterocolitis; Immune- mediated gastritis; Immune-mediated hepatic disorder; Immune-mediated hepatitis; Immune- mediated hyperthyroidism; Immune-mediated hypothyroidism; Immune-mediated myocarditis; Immune-mediated myositis; Immune-mediated nephritis; Immune-mediated neuropathy; Immune-mediated pancreatitis; Immune-mediated pneumonitis; Immune-mediated renal disorder; Immune-mediated thyroiditis; Immune-mediated uveitis; Immunoglobulin G4 related disease; Immunoglobulins abnormal; Implant site thrombosis; Inclusion body myositis; Infantile genetic agranulocytosis; Infantile spasms; Infected vasculitis; Infective thrombosis; Inflammation; Inflammatory bowel disease; Infusion site thrombosis; Infusion site vasculitis; Injection site thrombosis; Injection site urticaria; Injection site vasculitis; Instillation site thrombosis; Insulin autoimmune syndrome; Interstitial granulomatous dermatitis; Interstitial lung disease; Intracardiac mass; Intracardiac thrombus; Intracranial pressure increased; Intrapericardial thrombosis; Intrinsic factor antibody abnormal; Intrinsic factor antibody positive; IPEX syndrome; Irregular breathing; IRVAN syndrome; IVth nerve paralysis; IVth nerve paresis; JC polyomavirus test positive; JC virus CSF test positive; Jeavons syndrome; Jugular vein embolism; Jugular vein thrombosis; Juvenile idiopathic arthritis; Juvenile myoclonic epilepsy; Juvenile polymyositis; Juvenile psoriatic arthritis; Juvenile spondyloarthritis; Kaposi sarcoma inflammatory cytokine syndrome; Kawasaki’s disease; Kayser-Fleischer ring; Keratoderma blenorrhagica; Ketosis- prone diabetes mellitus; Kounis syndrome; Lafora’s myoclonic epilepsy; Lambl’s excrescences; Laryngeal dyspnoea; Laryngeal oedema; Laryngeal rheumatoid arthritis; Laryngospasm; Laryngotracheal oedema; Latent autoimmune diabetes in adults; LE cells present; Lemierre syndrome; Lennox-Gastaut syndrome; Leucine aminopeptidase increased; Leukoencephalomyelitis; Leukoencephalopathy; Leukopenia; Leukopenia neonatal; Lewis-Sumner syndrome; Lhermitte’s sign; Lichen planopilaris; Lichen planus; Lichen sclerosus; Limbic encephalitis; Linear IgA disease; Lip oedema; Lip swelling; Liver function test abnormal; Liver function test decreased; Liver function test increased; Liver induration; Liver injury; Liver iron concentration abnormal; Liver iron concentration

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5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

[con’t] [Liver iron concentration] increased; Liver opacity; Liver palpable; Liver sarcoidosis; Liver scan abnormal; Liver tenderness; Low birth weight baby; Lower respiratory tract herpes infection; Lower respiratory tract infection; Lower respiratory tract infection viral; Lung abscess; Lupoid hepatic cirrhosis; Lupus cystitis; Lupus encephalitis; Lupus endocarditis; Lupus enteritis; Lupus hepatitis; Lupus myocarditis; Lupus myositis; Lupus nephritis; Lupus pancreatitis; Lupus pleurisy; Lupus pneumonitis; Lupus vasculitis; Lupus-like syndrome; Lymphocytic hypophysitis; Lymphocytopenia neonatal; Lymphopenia; MAGIC syndrome; Magnetic resonance imaging liver abnormal; Magnetic resonance proton density fat fraction measurement; Mahler sign; Manufacturing laboratory analytical testing issue; Manufacturing materials issue; Manufacturing production issue; Marburg’s variant multiple sclerosis; Marchiafava-Bignami disease; Marine Lenhart syndrome; Mastocytic enterocolitis; Maternal exposure during pregnancy; Medical device site thrombosis; Medical device site vasculitis; MELAS syndrome; Meningitis; Meningitis aseptic; Meningitis herpes; Meningoencephalitis herpes simplex neonatal; Meningoencephalitis herpetic; Meningomyelitis herpes; MERS-CoV test; MERS-CoV test negative; MERS-CoV test positive; Mesangioproliferative glomerulonephritis; Mesenteric artery embolism; Mesenteric artery thrombosis; Mesenteric vein thrombosis; Metapneumovirus infection; Metastatic cutaneous Crohn’s disease; Metastatic pulmonary embolism; Microangiopathy; Microembolism; Microscopic polyangiitis; Middle East respiratory syndrome; Migraine-triggered seizure; Miliary pneumonia; Miller Fisher syndrome; Mitochondrial aspartate aminotransferase increased; Mixed connective tissue disease; Model for end stage liver disease score abnormal; Model for end stage liver disease score increased; Molar ratio of total branched-chain amino acid to tyrosine; Molybdenum cofactor deficiency; Monocytopenia; Mononeuritis; Mononeuropathy multiplex; Morphoea; Morvan syndrome; Mouth swelling; Moyamoya disease; Multifocal motor neuropathy; Multiple organ dysfunction syndrome; Multiple sclerosis; Multiple sclerosis relapse; Multiple sclerosis relapse prophylaxis; Multiple subpial transection; Multisystem inflammatory syndrome in children; Muscular sarcoidosis; Myasthenia gravis; Myasthenia gravis crisis; Myasthenia gravis neonatal; Myasthenic syndrome; Myelitis; Myelitis transverse; Myocardial infarction; Myocarditis; Myocarditis post infection; Myoclonic epilepsy; Myoclonic epilepsy and ragged-red fibres; Myokymia; Myositis; Narcolepsy; Nasal herpes; Nasal obstruction; Necrotising herpetic retinopathy; Neonatal Crohn’s disease; Neonatal epileptic seizure; Neonatal lupus erythematosus; Neonatal mucocutaneous herpes simplex; Neonatal pneumonia; Neonatal seizure; Nephritis; Nephrogenic systemic fibrosis; Neuralgic amyotrophy; Neuritis; Neuritis cranial; Neuromyelitis optica pseudo relapse; Neuromyelitis optica spectrum disorder; Neuromyotonia; Neuronal neuropathy; Neuropathy peripheral; Neuropathy, ataxia, retinitis pigmentosa syndrome; Neuropsychiatric lupus; Neurosarcoidosis; Neutropenia; Neutropenia neonatal; Neutropenic colitis; Neutropenic infection; Neutropenic sepsis; Nodular rash; Nodular vasculitis; Noninfectious myelitis; Noninfective encephalitis; Noninfective encephalomyelitis; Noninfective oophoritis; Obstetrical pulmonary embolism; Occupational exposure to communicable disease; Occupational exposure to SARS-CoV-2; Ocular hyperaemia; Ocular myasthenia; Ocular pemphigoid; Ocular sarcoidosis; Ocular vasculitis; Oculofacial paralysis; Oedema; Oedema blister; Oedema due to hepatic disease; Oedema mouth; Oesophageal achalasia; Ophthalmic artery thrombosis; Ophthalmic herpes simplex; Ophthalmic herpes zoster; Ophthalmic vein thrombosis; Optic neuritis; Optic

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5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

[con’t] [Optic] neuropathy; Optic perineuritis; Oral herpes; Oral lichen planus; Oropharyngeal oedema; Oropharyngeal spasm; Oropharyngeal swelling; Osmotic demyelination syndrome; Ovarian vein thrombosis; Overlap syndrome; Paediatric autoimmune neuropsychiatric disorders associated with streptococcal infection; Paget-Schroetter syndrome; Palindromic rheumatism; Palisaded neutrophilic granulomatous dermatitis; Palmoplantar keratoderma; Palpable purpura; Pancreatitis; Panencephalitis; Papillophlebitis; Paracancerous pneumonia; Paradoxical embolism; Parainfluenzae viral laryngotracheobronchitis; Paraneoplastic dermatomyositis; Paraneoplastic pemphigus; Paraneoplastic thrombosis; Paresis cranial nerve; Parietal cell antibody positive; Paroxysmal nocturnal haemoglobinuria; Partial seizures; Partial seizures with secondary generalisation; Patient isolation; Pelvic venous thrombosis; Pemphigoid; Pemphigus; Penile vein thrombosis; Pericarditis; Pericarditis lupus; Perihepatic discomfort; Periorbital oedema; Periorbital swelling; Peripheral artery thrombosis; Peripheral embolism; Peripheral ischaemia; Peripheral vein thrombus extension; Periportal oedema; Peritoneal fluid protein abnormal; Peritoneal fluid protein decreased; Peritoneal fluid protein increased; Peritonitis lupus; Pernicious anaemia; Petit mal epilepsy; Pharyngeal oedema; Pharyngeal swelling; Pityriasis lichenoides et varioliformis acuta; Placenta praevia; Pleuroparenchymal fibroelastosis; Pneumobilia; Pneumonia; Pneumonia adenoviral; Pneumonia cytomegaloviral; Pneumonia herpes viral; Pneumonia influenzal; Pneumonia measles; Pneumonia mycoplasmal; Pneumonia necrotising; Pneumonia parainfluenzae viral; Pneumonia respiratory syncytial viral; Pneumonia viral; POEMS syndrome; Polyarteritis nodosa; Polyarthritis; Polychondritis; Polyglandular autoimmune syndrome type I; Polyglandular autoimmune syndrome type II; Polyglandular autoimmune syndrome type III; Polyglandular disorder; Polymicrogyria; Polymyalgia rheumatica; Polymyositis; Polyneuropathy; Polyneuropathy idiopathic progressive; Portal pyaemia; Portal vein embolism; Portal vein flow decreased; Portal vein pressure increased; Portal vein thrombosis; Portosplenomesenteric venous thrombosis; Post procedural hypotension; Post procedural pneumonia; Post procedural pulmonary embolism; Post stroke epilepsy; Post stroke seizure; Post thrombotic retinopathy; Post thrombotic syndrome; Post viral fatigue syndrome; Postictal headache; Postictal paralysis; Postictal psychosis; Postictal state; Postoperative respiratory distress; Postoperative respiratory failure; Postoperative thrombosis; Postpartum thrombosis; Postpartum venous thrombosis; Postpericardiotomy syndrome; Post-traumatic epilepsy; Postural orthostatic tachycardia syndrome; Precerebral artery thrombosis; Pre-eclampsia; Preictal state; Premature labour; Premature menopause; Primary amyloidosis; Primary biliary cholangitis; Primary progressive multiple sclerosis; Procedural shock; Proctitis herpes; Proctitis ulcerative; Product availability issue; Product distribution issue; Product supply issue; Progressive facial hemiatrophy; Progressive multifocal leukoencephalopathy; Progressive multiple sclerosis; Progressive relapsing multiple sclerosis; Prosthetic cardiac valve thrombosis; Pruritus; Pruritus allergic; Pseudovasculitis; Psoriasis; Psoriatic arthropathy; Pulmonary amyloidosis; Pulmonary artery thrombosis; Pulmonary embolism; Pulmonary fibrosis; Pulmonary haemorrhage; Pulmonary microemboli; Pulmonary oil microembolism; Pulmonary renal syndrome; Pulmonary sarcoidosis; Pulmonary sepsis; Pulmonary thrombosis; Pulmonary tumour thrombotic microangiopathy; Pulmonary vasculitis; Pulmonary veno-occlusive disease; Pulmonary venous thrombosis; Pyoderma gangrenosum; Pyostomatitis vegetans; Pyrexia; Quarantine; Radiation leukopenia; Radiculitis

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5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

[con’t] [Radiculitis] brachial; Radiologically isolated syndrome; Rash; Rash erythematous; Rash pruritic; Rasmussen encephalitis; Raynaud’s phenomenon; Reactive capillary endothelial proliferation; Relapsing multiple sclerosis; Relapsing-remitting multiple sclerosis; Renal amyloidosis; Renal arteritis; Renal artery thrombosis; Renal embolism; Renal failure; Renal vascular thrombosis; Renal vasculitis; Renal vein embolism; Renal vein thrombosis; Respiratory arrest; Respiratory disorder; Respiratory distress; Respiratory failure; Respiratory paralysis; Respiratory syncytial virus bronchiolitis; Respiratory syncytial virus bronchitis; Retinal artery embolism; Retinal artery occlusion; Retinal artery thrombosis; Retinal vascular thrombosis; Retinal vasculitis; Retinal vein occlusion; Retinal vein thrombosis; Retinol binding protein decreased; Retinopathy; Retrograde portal vein flow; Retroperitoneal fibrosis; Reversible airways obstruction; Reynold’s syndrome; Rheumatic brain disease; Rheumatic disorder; Rheumatoid arthritis; Rheumatoid factor increased; Rheumatoid factor positive; Rheumatoid factor quantitative increased; Rheumatoid lung; Rheumatoid neutrophilic dermatosis; Rheumatoid nodule; Rheumatoid nodule removal; Rheumatoid scleritis; Rheumatoid vasculitis; Saccadic eye movement; SAPHO syndrome; Sarcoidosis; SARS-CoV-1 test; SARS-CoV-1 test negative; SARS-CoV-1 test positive; SARS-CoV-2 antibody test; SARS-CoV-2 antibody test negative; SARS-CoV-2 antibody test positive; SARS-CoV-2 carrier; SARS-CoV-2 sepsis; SARS-CoV-2 test; SARS- CoV-2 test false negative; SARS-CoV-2 test false positive; SARS-CoV-2 test negative; SARS- CoV-2 test positive; SARS-CoV-2 viraemia; Satoyoshi syndrome; Schizencephaly; Scleritis; Sclerodactylia; Scleroderma; Scleroderma associated digital ulcer; Scleroderma renal crisis; Scleroderma-like reaction; Secondary amyloidosis; Secondary cerebellar degeneration; Secondary progressive multiple sclerosis; Segmented hyalinising vasculitis; Seizure; Seizure anoxic; Seizure cluster; Seizure like phenomena; Seizure prophylaxis; Sensation of foreign body; Septic embolus; Septic pulmonary embolism; Severe acute respiratory syndrome; Severe myoclonic epilepsy of infancy; Shock; Shock symptom; Shrinking lung syndrome; Shunt thrombosis; Silent thyroiditis; Simple partial seizures; Sjogren’s syndrome; Skin swelling; SLE arthritis; Smooth muscle antibody positive; Sneezing; Spinal artery embolism; Spinal artery thrombosis; Splenic artery thrombosis; Splenic embolism; Splenic thrombosis; Splenic vein thrombosis; Spondylitis; Spondyloarthropathy; Spontaneous heparin-induced thrombocytopenia syndrome; Status epilepticus; Stevens-Johnson syndrome [Note by Celia Farber: “This, SJS, can result in the skin coming off the body altogether, from the body’s attempt to rid itself of poison.”]; Stiff leg syndrome; Stiff person syndrome; Stillbirth; Still’s disease; Stoma site thrombosis; Stoma site vasculitis; Stress cardiomyopathy; Stridor; Subacute cutaneous lupus erythematosus; Subacute endocarditis; Subacute inflammatory demyelinating polyneuropathy; Subclavian artery embolism; Subclavian artery thrombosis; Subclavian vein thrombosis; Sudden unexplained death in epilepsy; Superior sagittal sinus thrombosis; Susac’s syndrome; Suspected COVID- 19; Swelling; Swelling face; Swelling of eyelid; Swollen tongue; Sympathetic ophthalmia; Systemic lupus erythematosus; Systemic lupus erythematosus disease activity index abnormal; Systemic lupus erythematosus disease activity index decreased; Systemic lupus erythematosus disease activity index increased; Systemic lupus erythematosus rash; Systemic scleroderma; Systemic sclerosis pulmonary; Tachycardia; Tachypnoea; Takayasu’s arteritis; Temporal lobe epilepsy; Terminal ileitis; Testicular autoimmunity; Throat tightness; Thromboangiitis obliterans; Thrombocytopenia; Thrombocytopenic purpura; Thrombophlebitis; Thrombophlebitis migrans; Thrombophlebitis

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[con’t] [Thrombophlebitis] neonatal; Thrombophlebitis septic; Thrombophlebitis superficial; Thromboplastin antibody positive; Thrombosis; Thrombosis corpora cavernosa; Thrombosis in device; Thrombosis mesenteric vessel; Thrombotic cerebral infarction; Thrombotic microangiopathy; Thrombotic stroke; Thrombotic thrombocytopenic purpura; Thyroid disorder; Thyroid stimulating immunoglobulin increased; Thyroiditis; Tongue amyloidosis; Tongue biting; Tongue oedema; Tonic clonic movements; Tonic convulsion; Tonic posturing; Topectomy; Total bile acids increased; Toxic epidermal necrolysis; Toxic leukoencephalopathy; Toxic oil syndrome; Tracheal obstruction; Tracheal oedema; Tracheobronchitis; Tracheobronchitis mycoplasmal; Tracheobronchitis viral; Transaminases abnormal; Transaminases increased; Transfusion-related alloimmune neutropenia; Transient epileptic amnesia; Transverse sinus thrombosis; Trigeminal nerve paresis; Trigeminal neuralgia; Trigeminal palsy; Truncus coeliacus thrombosis; Tuberous sclerosis complex; Tubulointerstitial nephritis and uveitis syndrome; Tumefactive multiple sclerosis; Tumour embolism; Tumour thrombosis; Type 1 diabetes mellitus; Type I hypersensitivity; Type III immune complex mediated reaction; Uhthoff’s phenomenon; Ulcerative keratitis; Ultrasound liver abnormal; Umbilical cord thrombosis; Uncinate fits; Undifferentiated connective tissue disease; Upper airway obstruction; Urine bilirubin increased; Urobilinogen urine decreased; Urobilinogen urine increased; Urticaria; Urticaria papular; Urticarial vasculitis; Uterine rupture; Uveitis; Vaccination site thrombosis; Vaccination site vasculitis; Vagus nerve paralysis; Varicella; Varicella keratitis; Varicella post vaccine; Varicella zoster gastritis; Varicella zoster oesophagitis; Varicella zoster pneumonia; Varicella zoster sepsis; Varicella zoster virus infection; Vasa praevia; Vascular graft thrombosis; Vascular pseudoaneurysm thrombosis; Vascular purpura; Vascular stent thrombosis; Vasculitic rash; Vasculitic ulcer; Vasculitis; Vasculitis gastrointestinal; Vasculitis necrotising; Vena cava embolism; Vena cava thrombosis; Venous intravasation; Venous recanalisation; Venous thrombosis; Venous thrombosis in pregnancy; Venous thrombosis limb; Venous thrombosis neonatal; Vertebral artery thrombosis; Vessel puncture site thrombosis; Visceral venous thrombosis; VIth nerve paralysis; VIth nerve paresis; Vitiligo; Vocal cord paralysis; Vocal cord paresis; Vogt-Koyanagi-Harada disease; Warm type haemolytic anaemia; Wheezing; White nipple sign; XIth nerve paralysis; X-ray hepatobiliary abnormal; Young’s syndrome; Zika virus associated Guillain Barre syndrome.

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—Unless we rebel, someday this list will be engraved on a large memorial, and it will be framed in positive language, as an unparalleled achievement, as the introduction to the new genetically engineered human race.


power outside the matrix

(To read about Jon’s collection, Power Outside The Matrix, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

Murdering infants to obtain fetal tissue for vaccine research

An interview with AnnaMaria Cardinalli

by Jon Rappoport

November 4, 2021

(To join our email list, click here.)

For my recent series of articles on the murder of infants to obtain fetal tissue for vaccine testing and research, I gained key information from investigative reporter AnnaMaria Cardinalli’s article, “Catholic Conscience and the COVID-19 Vaccine,” in Crisis magazine.

AnnaMaria agreed to do an interview on this and related subjects. The interview speaks for itself—and it should provide people a VERY fundamental reason for rejecting the COVID vaccine.

Q: It seems you’ve lived at least several lives side by side. You’ve earned a lofty worldwide reputation as an operatic contralto and classical guitarist; you’re a licensed private investigator; you carried out extensive research for the US military in Afghanistan; you own a private security firm; you donate all your earnings to a Catholic order which wants to start an orphanage for exploited children. And I’m not covering all the bases. It’s rather mind-blowing. Before we dive into the subject at hand, can you speak to this variety and achievement?

A: Ha! Your question is very flattering and I’m hardly at issue here, but I’ll be happy to answer. The variety of work I’ve been involved in is so wildly unlikely that I could have never sat down and come up with it as a plan! The one factor underlying all it is my incredible fortune to have been raised soundly in the Catholic Faith by my mom, so despite my own many failings, I knew enough to put my life completely at the disposal of God’s will from an early age. I find utterly astounding the adventures on which He’ll lead a soul when He’s given that freedom. Making music was always my personal hope, but the rest came as a natural consequence of responding to circumstances around me with whatever capacities I had the ability to respond. That’s the very definition of responsibility (“response ability”), and a real means by which God guides our lives, don’t you think?

Q: In your wide range of experiences, did medical issues ever pop up on your radar?

A: Medical issues arose in two ways. On one hand, when I worked for the FBI and was embedded with the Joint Special Operations Command In Iraq, I received truly fantastic, cutting-edge training in a collateral duty as a Tactical Operational Medic. Later, in Afghanistan, I participated in medical missions to help assess rural tribal community needs—particularly the medical needs of women and children. Through these military experiences, I found a passion for emergency medicine. I recently re-certified as an EMT to better assist my community’s current medical mission to the homeless (sosvan.org), and I continue to pursue more advanced certifications.

On the other hand, I do not approach the issue of the cell line origins as a practitioner or any sort of medical expert, but as an investigative journalist, simply seeking out the facts and holding them to the light of common logic. My thinking is that the factors necessary to understand the nature of what we put into our bodies must be, at least on a basic level, accessible and comprehensible to the general population, and one need not be a medical expert to grasp them. Otherwise, how could most of us make an informed decision? We can’t allow clear, critical truths to be obfuscated by the statement, “You’re not an expert. You wouldn’t understand.”

Q: How did you become interested in the very specific origin of the fetal cell line, HEK 293? What made you think it might be important?

A: I was led to interest in HEK 293 via a long path. My experience in Afghanistan imparted to me a particular investigative focus on Human Trafficking. I’ve written and worked extensively on the issue, and the more I learn, the more I am overwhelmed by its prevalence, both internationally and on our own soil. In recent years, while the China Tribunal brought the harvesting and sale of organs belonging to unwanted citizens into clear focus overseas, the Planned Parenthood expose by David Daleiden [more on that expose — covered by investigative journalist Celia Farber, here and here] and others brought the same practice to light in the US. Both these developments solidified the trafficking issue in my mind not only as one of forced labor or sexual exploitation but of the complete commoditization of the human person—the viewing of the human being as a mere collection of occasionally useful parts, lacking any other value. This should frighten every person, regardless of their faith background or lack of one, because history shows us over and over again that it’s when we fail to recognize our common humanity that atrocities prevail.

With regard to HEK 293 specifically, for Catholics like myself, it is a grave moral responsibility to examine whether any action one takes participates in, perpetuates, or encourages such evil. We are bound to inform our own individual consciences and act in accordance with them. So, when the COVID vaccine became available, I sought to find out all I could about the nature of its origins and was led right back into the human trafficking concerns that plague me. It was in this research that I came across the work of the biologist and vaccine developer Pamela Acker [author of “Vaccination: A Catholic Perspective”; more here]. Her public acknowledgement of the necessary procedure for ensuring the viability of Human Embryonic Kidney (HEK) cells coincided with what medical professionals had shared with me privately.

For me, this was enough to raise concern that warranted further investigation before taking the vaccine. Sadly, the more the matter is investigated, as it was by the courageous, thorough, and insightful author of the Gateway Pundit article, the more evidence arises supporting my worst fear—that a perfectly innocent living child, a healthy little girl, born alive and outside the womb, was killed for and by the harvest of her organs, and that this is a practice that may underlie great parts of the research industry. Believe me, I am longing to find firm and indisputable confirmatory evidence that this nightmare scenario is NOT the case. However, your in-depth coverage of the subject following the Crisis and Gateway Pundit articles seems to continually contribute direct, expert-based medical evidence of the horrifying truth. Saddening as it is, I truly appreciate what you are accomplishing.

Q: The HEK (Human Embryo Kidney) 293 fetal cell line has been used to test COVID vaccines. That makes its origin vividly important now. How did you become convinced that the evidence pointed to the removal of an alive infant from her mother’s womb, and then the killing of that infant, in 1972, in the Netherlands, in order to harvest her kidneys—which would be used to create the HEK 293 cell line?

A: I reiterate that I had to be convinced by simple logic that anyone, not medical researchers exclusively, could follow. In fact, the more specialized the language describing a medical moral issue becomes, the more it can be used to obscure the facts. I would almost laugh, if not for the gravity of the issue, at hyper-euphemistic descriptions one finds in the medical literature. It discusses, for instance, situations like the finding of electrical impulses in the cardiac tissue of the POC.

First of all, “POC?” Product of conception? What a way to talk around an issue! I’m a proud product of conception and have never met anyone who wasn’t! Electrical impulses in the cardiac tissue? With fewer keystrokes, that could be called “a heartbeat.” So, I’m a POC with intact electrical impulses in my cardiac tissue or, if anyone were looking to save on ink, “alive.” Please, though, forgive my digression.

I worked to write very carefully in the Crisis article the simple facts that concerned me about the origins of the HEK 293 cell line. Rather than try to summarize that argument in this interview and thus potentially miss a critical component—may I please direct interested readers to the article at the link below?

Catholic Conscience and the COVID-19 Vaccine

I became further convinced of the reality following the publication of the Gateway Pundit exclusive which offered some insightful analysis taking into account the recent Pfizer whistleblower revelations. I’d also like to direct anyone interested to that great article with a link below.

Exclusive: Pfizer’s Nervousness About Its COVID Vaccine’s Origins Conceals a Horror Story

It’s not that I don’t want to answer the question, it’s that I want it to be answered as accurately as possible.

Q: When I read conventional medical literature that describes research on aborted fetuses, I see no mention of taking the infant from the mother’s womb, alive, and then killing him/her. Is this a research “open secret” that is held back from the public and even many doctors? I read a 1975 federal report on medical research using fetuses. It went on for a hundred pages, and there wasn’t one reference to killing infants in the process of removing their organs.

A: I think the first issue here is the extremely removed language typical of the descriptions of these procedures that I reference above, along with its tendency to state actions separate from their obvious consequences. It’s a linguistic tendency that may well reflect the thinking and training of researchers and abortionists. In Dr. Kathi A. Aultman’s testimony to the Senate Judiciary Committee Hearing on March 15th 2016, which you excerpted in your incredibly revealing post of October 27th [see here; more here], the doctor describes her initial fascination with the cellular perfection of the little bodies she dissected, and explains that it was only years later that was she able to overcome her scientific dissociation to make the intellectual connection that the tiny perfect bodies were those of people whose lives she had ended.

I worry our society has removed death so far from life that we don’t even recognize it, and that is a scary thing. Our grandparents die in facilities away from home rather than with their hands held in ours. Our food arrives packaged and devoid of any reminders of the animals from which it came. Fido moves to a faraway farm, while we play immersive games where graphically taken lives merely “reset.” Therefore, unlike any generation prior to ours, most of us can go through life without regularly witnessing the reality of death, which makes for a very unnatural understanding of it—one far from the Catholic motto of memento mori. It’s an understanding that might even allow a scientist to admire a human body on which she performed a procedure that ended the function of its “cellularly perfect” organs without grasping that she was its killer.

I suspect this kind of thinking in turn produces academic writing in which it is almost impossible to see anything untoward. Perhaps most authors themselves can’t see it, aside from the presumably rarer instances of dedicatedly evil individuals who do see things clearly and actively choose to obfuscate the reality. Either way, this is why the literature will never say, as you had difficulty finding, “in the next step, kill the newborn,” even if it is the obvious consequence of the procedure described.

If the doctors involved were capable of that kind of cause-and-effect thinking, perhaps they would have to first write, “in the next step, first anesthetize, then kill the newborn.” If some of those doctors believed themselves Christians, they would have to write “in the next step, first baptize, then anesthetize, and then kill the newborn.” Even if they believed themselves merely in possession of basic mammalian instincts, they would at least have to write “in the next step, first cuddle and comfort the crying newborn, then anesthetize and kill him.” Of course, they can’t go there without recognizing the child’s humanity, so instead, the scientific dissociation of cause-and-effect remains in place.

This critical thought barrier is evidenced particularly in the literature when we see organs harvested from living children outside the womb referred to as fresh “fetal” or even “embryonic” tissue. The biomedical research companies requisitioning the tissue make the same linguistic error and it goes constantly uncorrected. No. The medical term for a delivered fetus in its first moments and days of life outside the womb is a neonate. A newborn. Most of these people went to medical school and know the difference, but they persist in the error.

Perhaps if we could only require them to accurately use the language of “fresh neonatal tissue” in their requisitions and reports, some would be unable to proceed. Requesting a “heart of newborn” for the development of whatever a researcher might be concocting in the lab might finally sound to the ears of many too much like procuring the ingredients of a witch’s brew belonging to horror fiction. It certainly makes “eye of newt” sound resoundingly tame.

Other than the issue of logic and language, however, I don’t think the practice of infanticide by vivisection is particularly secret among those working closely in the arena of biomedical research, and it’s certainly known among the abortionists who supply the needs of the industry, although I agree with you that it’s not something that doctors whose scope never intersects the arena are aware of any more than most of us are. It’s simply not brought to our attention in the media. We focus where the media points us, and there appears some decided silence on the issue.

A breakthrough in public awareness of the direct killing of living unwanted newborns for the sake of biomedical research, which, almost incomprehensibly, generated far less media attention and public outcry than it should have, occurred with the David Daleiden hearings. There many doctors and scientific procurement company representatives spoke openly of the practice, though often in the detached terms that would require careful listening. For instance, the CEO of Stem Express admitted dryly that “fetal hearts were perfused using a Langendorff apparatus.”

A Langendorff apparatus serves to preserve the functional viability of hearts ex-vivo (which means, literally, outside of a living body). That is, to specify the use of the Langendorff apparatus is to know that a heart requiring this preservation was, in fact, taken from a living body. To state the painfully obvious cause-and-effect reasoning generally left out here, the removal of a functioning vital organ from a living person (without the replacement of its function) is the direct killing of that person. No example is clearer than that of a beating heart. Ask an Aztec.

Dr. Theresa Deisher, a Stanford University School of Medicine researcher heavily involved with the use of adult stem cells, describes exactly how that killing must take place in order for the Langendorff perfusion to function. Both in her September 19th, 2019 testimony at the Daleiden trial and in a same-day interview with Lifesite News, she explained that the individuals performing the vivisection would necessarily “cut open the baby’s chest and they would take the heart out beating and drop it in a buffer with potassium. She went on to state with rare clarity, “of course, if the heart isn’t beating, they can’t get any of these cells. Nobody wants a stopped heart.” [more, here]

At another point in her testimony she explained again that, “some of the babies had to have beating hearts when they were harvested.” Logic alone dictates this fact, as she explained “once the heart goes into contraction, you can’t get it to come out of that position.” It “has to be beating and be arrested in a relaxed position” to be of use for research purposes.

Again, just with the use of basic reason, it goes without saying that not only are breathing hearts being removed, but that these procedures occur on living children outside the womb, not within it. The people doing the dissection are not opening the chest of the child in the sort of incredibly rare and highly specialized in utero surgery that might be done to repair a fetal heart condition. The cost and specialization would be astronomical and nonsensical, as they intend to destroy the child, not save it.

So, just by using the single example of hearts on the Langendorff apparatus, which is to say nothing of the “embryonic” kidney cells, (which may more accurately be called “neonatal” kidney cells) used in the COVID vaccine testing and development, I think I can answer your question by saying there is no “open secret” regarding infanticide for medical research. There is no secret at all. I am not revealing anything that is not already obvious, even to a non-expert, given to looking at the simple facts.

The shocking thing, at this point, is not that this is happening, but that we have yet to react, as a whole, in opposition to it. In fact, we accept it by welcoming into our lives the “benefits” of the tortuous murders of innocent children. If we are doing this unknowingly, then perhaps it is because we have bought into the suspension of cause-and-effect reasoning like that to which the researchers subscribe.

Your question leads me, however, to one more point, which I hope provides a wake-up point if nothing else has. Even more shocking than our acceptance of this evil is the fact that it is entirely unnecessary. We could have the same or perhaps greater benefits by other means, but we don’t pursue the course of action that has proven successful in halting unethical bioresearch before and redirecting the course of the industry.

Why don’t we do for our own species what we have succeeded in doing for animals? Most people recognize that animal advocacy and speaking with our wallets through the boycotting of unethically-produced products is genuinely critical because lab animals are innocent creatures who cannot speak for themselves. Isn’t that true of human “lab babies” too?

Also in the expert testimony cited above, Dr. Deisher made the point that using human fetal tissue for research has become more prevalent because increasing regulations on the welfare of animals have made the use of humans more convenient. More convenient! In a way, while horrifying, this is also wonderful news, because it means that animal activists successfully changed things, albeit with a terrible unexpected outcome. However, it means that we can do the same for our species too!

Does that mean that the kind of beneficial research advances which have previously come from the study of neonatal tissue need to stop? Do we have to decide on a sacrificial trade off, with improvement in the lives of those with debilitating illnesses on one hand and the murder of human babies with less compassion than lab rats on the other? Is that how science must proceed—in sanitized facilities behind closed doors that, just in case we become personally in need of its “benefits,” we prefer not to give much thought?

Here’s another shocker. Not at all. Adult pluripotent stem cells, obtained with adult consent and with no need for tortuous murders, actually negate the necessity of the use of fetal organs for stem cell research, because they can be cultured into any type of body cell. This technology exists now, but its use is more costly and less common than the worn-in ease of the baby butchering business. However, like any emerging technology, the more its use expands, the lower its costs become.

We can be the drivers of the expansion of its use, by making unethical research the expensive and inconvenient option. When I was a little girl, I was horrified to learn that lipsticks were tested on mistreated lab rabbits and resolved to never condone that practice with my purchase. So did every little girl I knew. Now cruelty-free cosmetics are the expected and affordable norm. Please, if we could ban together as a caring society to save the bunnies, what should we be willing to do to save the babies?


The Matrix Revealed

(To read about Jon’s mega-collection, The Matrix Revealed, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

California, you had your chance to recall Newsom; now he’s putting the poisoned needle into all your children

by Jon Rappoport

October 4, 2021

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Gavin Newsom is your vampire, California.

His new mandate for injecting devastating COVID vaccines into all schoolchildren in 7th grade and above—which will eventually be expanded to ALL schoolchildren—is a gold rush quite different from the 19th century voyage.

This one is pharmaceutical-profit gold.

Maybe the following self-congratulatory and forward-looking business statement from the state government, on its website, has something to do with Newsom bringing down his doomsday machine on millions of innocent children:

“California has a history of leading innovations in life-saving biomedical technologies. We are the long-time home to the nation’s number 2 biomedical sciences research institution and at nearly $4 billion annually, California’s universities lead the US in earned National Institutes of Health grants.”

“California’s life sciences industry generates nearly 1 million direct and indirect jobs and over $178 billion in annual revenue. More bioscience and biotechnology patents are issued to California companies and researchers than any other state. California leads the pack across the board for patent generation from microbiology and genetics to bioinformatics and health IT – creating more than 2.5 times as many patents as the next ranking state.

California life science companies saw over $18B in venture capital investment from 2016 – 2018, more than any other state, and our businesses have 1,300+ therapies in the development pipeline. These investments keep California at the forefront of biotech innovation.”

Newsom is one of those creatures who mistakenly believes he is physically attractive. And this, he reasons, is an asset he should deploy whenever possible.

In point of fact, he resembles a synthetic hothouse low-hanging fruit that is turning bad under the skin.

He also thinks his earnest front is believable. Please. Only the deaf, dumb, and blind assume his mission in life is “helping.” But apparently, many such disabled souls live in California.

And they are ready to sacrifice their children to him.

Newsom is a leftover Yuppie from the 1980s. Genial, relaxed, cold, mad for more power. I assure you, if the day comes when he senses a real threat to his position, he’ll turn out the lights in California. He’ll bring on an Australian-style lockdown.

The VAERS count of COVID vaccine injuries in American has risen past 700,000. As acknowledged by the well-known Harvard Pilgrim Healthcare study, reported vaxx injuries should be multiplied by a hundred to arrive at an accurate figure.

Newsom takes no notice of this. He’s living in his own bubble, and seeks glory from colleagues and friends who occupy the same bubble and shower him with praise. For the record, if there is a record anymore, this makes him quite dangerous.

But look who I’m talking to. Californians.

Don’t worry, be happy. It’s all good.

The state of California lives under a lucky star. Big tech, big movies, big defense industry, big pharma.

Maybe your children, commanded to take the shot, will somehow scrape by. No mind-boggling “unexplainable” heart problems. Perhaps only micro-clots, whose effects won’t show up until later…and then, who would be able to point to you, the parents, as collaborators?

All the nurses who are refusing the injection, even though that means they’re being fired from their jobs and losing their careers…what do they know? They’re obviously just a bunch of ingrates.

And with a man like Gavin Newsom at the helm
Why o why would you be lying in bed at night sweating
Waiting for the sun to come up
The sun that cures all problems in California
Why would you sense you’re sinking into deeper darkness
And you have to make a move to save your soul
And rescue your children
Why would you wonder how you arrived at the crossroads
When the people you know aren’t concerned at all
There must be some mistake
You need a small dose of reprogramming and then
The world will resume its former shape
As it always does
Especially in California
The guns in your mind will go silent
The governor is equipped to do the right thing
He must be
Otherwise the whole STRUCTURE was built
To capture you and your children
Look at the dawn
Look at the sun
The Pacific rolling in
The white houses sitting on the cliffs
The time is exactly right for another day
Like other days
And that is your strongest clue
Pointing to the need for censoring from your mind
Possibilities over which you have no control
As you well know
Everything beyond your control in California
Is good
That’s what living in California has always meant
And this is what the smile on Gavin Newsom’s face tells you
So send your child into the line
Of fire


The Matrix Revealed

(To read about Jon’s mega-collection, The Matrix Revealed, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.