https://townhall.com/tipsheet/spencerbro...o-n2598970

The CEO of Pfizer (market cap: $240.5 billion) is Albert Bourla (2020 compensation package: $21 million). Bourla and his colleagues want your kids to start getting jabbed with his company’s COVID vaccine by Thanksgiving. Triumphant after the Biden administration last week approved Pfizer’s COVID booster shots (estimated global sales: $26 billion), the company is touting study results (preliminary and non-peer-reviewed), which purportedly show “robust” antibody response and “favorable” safety outcomes for children ages 5-11 who received a two-dose combo in clinical trials.

Now, here are some facts all moms and dads must know about Pfizer before they allow their young daughters and sons to be guinea pigs of a profit-maximizing multinational corporation.

Twenty five years ago, Pfizer sent a team to Kano, Nigeria during a meningococcal meningitis outbreak. They conducted an “open label” (unblinded) clinical trial involving 200 children, half of whom were given Pfizer’s new antibiotic Trovan and half of whom received the gold standard treatment, ceftriaxone. Watchdogs noted that Pfizer used substantially lower doses of ceftriaxone to rig the trials in favor of Trovan.

At the time of the Kano trial, Pfizer was pushing for FDA approval of their latest potential billion-dollar cash cow for pediatric use. Eleven Nigerian children died: five after receiving Pfizer’s product and six after receiving lower-than-normal doses of the older drug.

Pay close attention, parents. A Washington Post investigation reported that one 10-year-old girl suffering from meningitis was not taken off experimental Trovan and given standard, proven treatments by Pfizer’s clinical trial operators–when it was clear that her condition was deteriorating. One of her eyes froze. She lost strength, then died. A Nigerian doctor who supervised the studies for Pfizer admitted that his office had “backdated an approval letter” for the human trials, which “may have been written a year after the study had taken place.” Informed consent was undermined by language and education barriers.

One outraged African newspaper demanded that the government “tell us whether our children were used as guinea pigs and, if so, who committed such criminality and who is liable.” After years of protracted litigation with the pharmaceutical behemoth, Nigerian families reached a $75 million out-of-court settlement sealed with a confidentiality clause.

A separate whistleblower lawsuit filed by Pfizer’s former associate medical director for central research and Yale pediatric infectious disease specialist, Juan Walterspiel, alleged that the company fired him in retaliation for warning before and after the deadly Kano fiasco that the study methods were “improper and unsafe.” Walterspiel further claimed that Pfizer had bribed Nigerian officials to continue the study and cut safety corners because “stock options and bonuses were at stake.”

Pfizer tried to suppress Walterspiel’s allegations, but was forced into a settlement after Wikileaks published diplomatic cables showing that Pfizer had attempted to dig up dirt on a Nigerian prosecutor to bully him into dropping lawsuits by state and federal authorities in Africa.


A secret internal Nigerian government report, leaked years after it had been written, concluded that Pfizer violated international law by conducting an “illegal trial of an unregistered drug” and failing to inform children’s parents that the meningitis treatment was experimental. The government panel called the Trovan tragedy a “clear case of exploitation of the ignorant.”

If you think this corruption was all an anomaly, or misunderstood altriuism, or “misinformation,” I encourage you to start doing your own homework before your child’s health and life become just another cost of doing Big Pharma Business.

Search the Internet and PubMed (while you still can) for “Pfizer,” “Celebrex,” “Bextra,” “Geodon,” “Zyvox,” “Lyrica,” and “Neurontin.”

Find out more about why Pfizer paid the largest fine for health care fraud in American history ($2.3 billion) in 2009 to resolve allegations that it illegally caused false claims to be submitted to the government and paid kickbacks to health care providers to induce them to prescribe their products.

Learn more about the nearly 3,000 people who developed suicidal thoughts and severe psychological disorders after taking Pfizer’s smoking cessation drug, Chantix. Pfizer paid out nearly $300 million to settle those cases. Or the nearly 10,000 women who won claims of nearly $1 billion after developing breast cancer linked to Pfizer’s Prempro hormone replacement therapy.

And just remember, parents, that the pandemic profiteers who stand to gain unprecedented, multi-billion-dollar windfalls from endless vaccine boosters administered cradle to grave around the world have the most terrifying man-made immunity ever created: immunity from liability for their corner-cutting, life-endangering business model.

Parents: Protect your children at all costs from Big Pharma so your children’s lives don’t become costs of Big Pharma doing business.

The White House’s official press release announcing the Build Back Better Act (BBB) pitches it as a “PLAN TO REBUILD THE MIDDLE CLASS.” It rhapsodizes about “working families” squeezed by the economy, and reminds voters that “Biden promised to rebuild the backbone of the country — the middle class.”

A cartoon illustrates the sort of person who would benefit from Biden’s Build Back Better programs: “Linda,” a white woman, who works at a manufacturing plant but struggles to raise her son, “Leo.”

One thing the White House’s official press release did not mention is that almost all of the $2 trillion doled out under BBB is expressly designated for Black, Latino, Native American, Asian American, Pacific Islander and non-English speaking individuals. White Americans will get nothing and like it.

“Even provisions that don’t explicitly exclude whites, turn out, on closer examination, to exclude whites.”
Over and over again, the bill is written expressly NOT to help the hardworking Linda, apparently because she is white. Here are just a few examples:

— $1 billion to Native American, Alaska Native and Native Hawaiian communities for housing “needs.”

— $500 million for minority-serving schools of medicine.

— $112 million for teacher preparation programs at Historically Black Colleges and Universities (HBCUs) and Minority Serving Institutions (MSIs).

— $75 million for culturally appropriate care management and services for older individuals who are racial and ethnic minorities or are underserved due to sexual orientation or gender identity.

— $75 million to study maternal health for pregnant and postpartum minority individuals.

— $50 million study maternal mortality among minorities.

— $50 million to improve behavioral health outcomes for communities of color with substance abuse.

— $75 million to increase research capacity at minority-serving institutions.

And on and on and on.

The very first item in Title II of the bill, titled “ELEMENTARY AND SECONDARY EDUCATION,” is a program to distribute more than $100 million in grants to address “low diversity within the teacher and school leader workforce.” To be eligible for a grant, the recipient must have a plan “to increase the diversity of qualified individuals entering into the teacher, principal, or other school leader workforce.”

Similarly, the first provision of BBB’s “ECONOMIC DEVELOPMENT” section is: “Minority Business Development Agency.”

But wait — here’s a plot twist! This part also includes something for rural America! (So Democrats have heard of Appalachia.) Twenty-one percent of the country is rural. Twenty-four percent is non-white. Guess how the money is divvied up?

One billion dollars for minorities and $200 million for “rural business centers.”

Even provisions that don’t explicitly exclude whites, turn out, on closer examination, to exclude whites. I’ve never seen so many synonyms for “non-white,” such as “persistent poverty communities,” “historically economically distressed,” “historical injustice” and “underserved communities.”

Hang on, Ann — what makes you think “underserved” means “non-white”?

I refer you to page 111 of the bill:

“This section also defines an ‘underserved community’ as a group of people who have been systematically denied the full opportunity to participate in aspects of economic, social, and civic life. Underserved communities include Black, Latino, Indigenous and Native American persons, Asian American and Pacific Islanders, other persons of color, [etc.].”

How about changes to our environmental laws? White people love the environment! Sorry, out of luck, again, white boy.

BBB allocates almost $7 billion for “national service programs to carry out projects related to climate resilience and mitigation.” Unfortunately, however, all those billions have to go to “entities that serve and have representation from low-income communities …; utilize culturally competent and multilingual strategies; … implemented by diverse participants from communities being served.”

One billion dollars of the “Climate Resilience and Mitigation” loot is specifically directed to “individuals who were formally incarcerated.” [Sic.] Sure, climate change is important — but not as important as giving money to convicted felons!

What the hell happened to Linda?

Linda is wearing a hardhat, so her job has probably been outsourced. Maybe she’ll be helped by BBB’s humongous expansion of the Trade Adjustment Assistance program (TAA). That’s the law passed in the 1960s to compensate American workers whose jobs have been shipped abroad by globalist swine who couldn’t care less about their fellow Americans and don’t mind that every single thing we need, including masks and medicine, is made in China.

Surely, some white people will qualify for that — steelworkers, autoworkers, glass, plastic and paper manufacturing employees.

In fact, the BBB hijacks the whole idea of compensating globalism’s losers and turns the TAA into just another massive welfare scheme. Both the eligibility requirements and payment amounts are expanded beyond all reason, entitling “workers” to years and years of payouts, with no minimum employment period required, and no stipulation that trade has anything to do with the loss of their jobs.

Thus, for example, a program that is — again — meant to remunerate workers whose jobs were shipped abroad will now offer assistance to public sector employees. How does a government employee lose a job at all — much less to trade? (I only wish we had Chinese people running our grade schools.)

Naturally, states will be required to work with “training providers” that have a proven track record serving “Black, Latino, Indigenous and Native American persons, Asian American and Pacific Islanders, other persons of color, members of other minority communities” and so on.

Republicans seem to think that if they just talk about how much Biden’s BBB plan costs, their job is done. They ought to read the bill. It might prompt them to finally say something about the Democrats’ clear animus against white Americans.

Conservatives Are Just Openly Endorsing Book Burning Now | Vanity Fair

Why can't anyone explain how these 14 kids died after getting vaccinated?

On July 16, 2021, the CDC looked into the deaths of 14 kids in VAERS who died after vaccination. 
https://stevekirsch.substack.com/p/why-c...-how-these


Taiwan blocks second Pfizer doses for teens

And they aren't even CONSIDERING allowing kids 5-11 to get Covid vaccinated at this point
https://alexberenson.substack.com/p/taiw...izer-doses



New VAERS analysis reveals hundreds of serious adverse events that the CDC and FDA never told us about

They missed hundreds of serious adverse events that are more elevated than myocarditis. A new VAERS analysis done by Albert Benavides blows the doors off the "safe and effective" narrative.
https://stevekirsch.substack.com/p/new-v...s-hundreds

Fricking horses asses
https://www.bitchute.com/video/qwBdWkD8FaFu/

And where is the outrage of these assholes for trying to film the jurors to get them to come to a guilty verdict by doxxing them.

Newsmax Host Eric Bolling Rages Over Big Bird and Vaccines, Says ‘Sesame Street Are a Bunch of Communists!’ (thedailybeast.com)

Quote:Newsmax host Eric Bolling eagerly jumped aboard the right-wing ragefest over Big Bird promoting vaccines, declaring on Monday that “Sesame Street are a bunch of communists” for “hawking the jab to five-year-olds.”

Over the weekend, CNN ran a TV special on COVID-19 vaccines aimed at children and parents, featuring characters from the seminal children’s program Sesame Street. With the CDC now recommending children ages 5 to 11 get vaccinated, the special included experts like the U.S. surgeon general answering questions from kids about the safety and efficacy of the jab.

Quote:At the same time, Big Bird—whose character is meant to be six years old, mind you—noted that he had gotten the shot, as he had only recently become eligible. And once the Twitter account representing the iconic character (who is, again, a fictional talking bird played by a person inside a large costume) posted that he was vaccinated and that “it'll give my body an extra protective boost that keeps me and others healthy,” the right-wing freakout began.

Sen. Josh Hawley defends speech on porn and video games - Axios

Quote:Sen. Josh Hawley (R-Mo.) told "Axios on HBO" he'll make masculinity a signature political issue, because he claims "the left" is telling men: "You're part of the problem. ... Your masculinity is inherently problematic."

Why it matters: As an ambitious Republican frequently mentioned as a possible future candidate for president or vice president, Hawley, 41, is using American masculinity to appeal to suburban parents, and to working men won over by Donald Trump.

Malfeasance Behind the FDA Vax OK for Children 

Malfeasance Behind the FDA Vax OK for Children
By F. William Engdahl
1 November 2021
On October 27 the US Food and Drug Administration Advisory Panel on Vaccines recommended the agency allow Pfizer to amend its Emergency Use Authorization for its COVID vaccine to include children 5 through 11 years old. Two days later the FDA officially approved the rollout. Major media are treating this as a positive development to protect young children. On closer inspection it is anything but that. The FDA is today shockingly corrupt under the Acting Director and is little more than a rubber stamp for Big Pharma, and especially Pfizer, where the former FDA head sits on the board .

The FDA’s Vaccines and Related Biological Products Advisory Committee voted 17 to 0, with one abstention, to give a green light allowing Emergency Use Authorization for the Pfizer-BioNTech experimental mRNA to children between 5 and 12 years. The expert who abstained later explained he did so because of limited safety and efficacy data provided. Previously the FDA had approved the vaccine for 12 and older. Adding to the stench of corruption around the latest vote, the Biden Administration a week earlier announced it had already purchased enough Pfizer vaccine to inoculate all 28 million 5- to 11-year-olds in the US. Did they know the fix was in?

‘…Just the Way it Goes’

The record of the FDA, the major drug oversight agency in the US Government, regarding safety and risks of the experimental gene-altered mRNA vaccines of Pfizer, is one of criminal malfeasance, defined as willful violation of a public trust or obligation that causes harm or death. Their latest ruling is even more egregious for blatant conflicts of interest and scientific fraud. Both Pfizer, who conducted the tests on the efficacy of their own vaccine on the 5-11 year age group, and the FDA experts, admitted that they had no idea if the vaccine was safe for such a young population.

Dr. Eric Rubin, professor of immunology at the Harvard T.H. Chan School of Public Health voted to approve the Pfizer-BioNTech vaccine, noting, “The data show that the vaccine works and is pretty safe … and yet we’re worried about a side effect that we can’t measure yet, but it’s probably real.” That is hardly confidence-building. He then stated, “we’re never going to learn about how safe this vaccine is unless we start giving it. That’s just the way it goes.”

This cold-blooded nonchalance is even more astonishing in light of the fact that the incidence of serious side effects in the 5-11 age group who allegedly have tested positive for the corona virus is essentially zero. According to data of the US Government Centers for Disease Control, the Infection Fatality Rate for children from 0-17 years is 0.0002 per 100,000 and far lower for the 5-11 years. A research study by Johns Hopkins University found that risk of severe illness or death from covid19 in a study of 48,000 children is essentially zero if no other morbidity risk such as leukemia, diabetes or asthma is present. Moreover, risk of infecting other children is also very low.

In their submission to FDA for approval, Pfizer stated the vaccination was needed for the 5-11 age group to prevent covid disease transmission. Yet in their FDA hearing on questioning, Dr. William Gruber, senior vice president of Pfizer Vaccine Clinical Research and Development, said they did not even assess whether the vaccine prevents transmission. We might ask why is this at all needed then if the risk to children is zero and there is no evidence of children transmission?

Even more shocking is the statement by Pfizer about its tests. First there were no animal tests on rats or such first. They admitted that the tested human group was so small that they could not test for myocarditis or pericarditis. Yet those are among the most reported negative effects for all others that have had the Pfizer jab. In its FDA application Pfizer noted that the number of participants in the current clinical development program was “too small to detect any potential risks of myocarditis associated with vaccination,” and that “to evaluate long-term sequelae of post-vaccination myocarditis/pericarditis” in participants 5 to less than 12 years of age will not be studied until after the vaccine is authorized for children.”

Flawed Pfizer Tests

The tests Pfizer made were also fatally flawed. According to Dr. Josh Guetzkow, of the Hebrew University of Jerusalem, the Pfizer study was not double-blind. Further, Pfizer cherry-picked subjects to evidently better their results. Three thousand children age 5-11 received Pfizer’s COVID vaccine, but only 750 of those children were selectively included in the company’s safety analysis. And Pfizer dismissed cases with adverse vaccine effects in their FDA filing: “Few serious Adverse Events, none of which were related to vaccine, and no AEs leading to withdrawal were reported.” They give no explanation how that was determined. Just trust Pfizer.

And post-vaccination follow up was less than 2 months for one test cohort and only 2.4 weeks for a second. The Pfizer report to FDA read, “Supplemental safety expansion group data were analyzed from approximately 1500 vaccine recipients with a median follow-up time of 2.4 weeks after Dose 2. These supplemental data demonstrate an acceptable safety profile…” It can take months or longer for side effects to manifest. Vaccine experts recommend at least 18-24 month post-vaccine follow up, not 3 months or 2.4 weeks. This is not serious science.

As well, it seems the FDA and or Pfizer wrongly name the vaccine in the title as “BNT162B2 [COMIRNATY (COVID-19 VACCINE, MRNA)] .“Yet the actual FDA text calls it “Pfizer-BioNTech COVID-19 Vaccine (BNT162b2).”

The separate company, BioNTech of Mainz, Germany, has a similar but “legally different” vaccine, trade-named Comirnaty, that is not available in the USA. The distinction is essential as it was the basis in August for the corrupt FDA to give Pfizer-BioNTech vaccine an extension of Emergency Use Authorization but to misleadingly declare its full approval for Comirnaty vaccine of BioNTech. This is deliberate fraud and allowed the Biden Administration to mandate vaccination of US government workers (curiously except for White House and Congress), military, and any company with more than 100 employees.

Conflicts of Interest?

The corruption of the FDA extends to the members of the Vaccine Advisory Committee. Many of the members of the current 18 person committee have direct ties to Pfizer or to the pro-Pfizer Gates Foundation.

Prof. Holly Janes of the Fred Hutch Cancer Research Center in Seattle designed the flawed Pfizer tests. Her institute is funded by Gates Foundation money. FDA committee member Dr. Steven Pergam is also with the Gates-funded Fred Hutch center. Acting committee chair, Arnold S. Monto was a paid consultant to Pfizer. Committee member Archana Chatterjee worked on a Pfizer research project related to vaccines for infants between 2018-2020. Geeta K. Swamy is chair of the “Independent Data Monitoring Committee for the Pfizer Group B Streptococcus Vaccine Program,” a committee sponsored by Pfizer. Duke University states that “Dr. Swamy serves as a co-investigator for the Pfizer COVID-19 vaccine trial.” FDA Committee member Gregg Sylvester was a vice president for Pfizer Vaccines. Ofer Levy, professor of pediatrics at Harvard Medical School is on record vigorously supporting Pfizer covid vaccines for children 12 and older. And FDA committee member Paul Offit professor of pediatrics at The Children’s Hospital of Philadelphia called openly last June for covid vaccine permission for children.

When we compare the actions of corrupt FDA Acting Director Janet Woodcock during the August FDA extension of emergency use authorization for Pfizer-BioNTech vaccine, she refused then to even allow the vaccine committee to meet to debate the issue. Several months before in June 2021 three members of the FDA Vaccine Committee resigned in protest over Woodcock’s refusal to heed the near unanimous vote of the advisory committee to approve an Alzheimer’s drug called Aduhelm against the wishes of nearly every member on the panel.

Clearly Woodcock has been busy in the meantime stacking the advisory committee with pro-Pfizer members. Not to be forgotten is the fact that after he left as head of the FDA under Trump, Scott Gottlieb immediately joined the board of directors of…Pfizer Inc. Woodcock served under him at FDA.

Woodcock has been at FDA since 1986, almost as long as Fauci at NIAID. Woodcock was Biden’s choice to head FDA, but a massive opposition from 28 groups including state attorneys general and citizen groups forced him to name her “acting,” which does not need Congressional scrutiny. Woodcock was directly responsible for the original FDA approval of deadly opioids over the objections of her own scientists and other advisors.

Already California has moved to make public school admission contingent on covid vaccination, anticipating Pfizer approval. This spread of the deadly Pfizer vaccine to children who have near zero risk of serious disease makes no public health sense. It is simply prima facie evidence of medical malfeasance at the highest levels of the US Government including FDA, with plausible criminal intent. The FDA decision will now be used to argue for similar inclusion of essentially no risk children for the vaccine jab

The Wall Street Journal is reporting that vaccine makers and U.S. healthcare officials are now attempting to find out why the mRNA vaccines are creating adverse events and heart conditions in healthy people.  Call me crazy, but studying dangerous side-effects would seem to be a more prudent line of inquiry before injecting people, not after.

Wall Street Journal – […] Researchers aren’t certain why the messenger RNA vaccines, one from Pfizer Inc. and partner BioNTech, and the other from Moderna Inc., are likely causing the inflammatory heart conditions myocarditis and pericarditis in a small number of cases.

Some theories center on the type of spike protein that a person makes in response to the mRNA vaccines. The mRNA itself or other components of the vaccines, researchers say, could also be setting off certain inflammatory responses in some people.  One new theory under examination: improper injections of the vaccine directly into a vein, which sends the vaccine to heart muscle.


To find answers, some doctors and scientists are running tests in lab dishes and examining heart-tissue samples from people who developed myocarditis or pericarditis after getting vaccinated. (read more)

Meanwhile, the rush to vaccinate children, with an untested vaccine as a treatment to protect against a virus that poses no significant threat, is continuing.