BAM: Famous Doctor Exposes FDA Ivermectin Lies

BY RENEE NAL

SEE: https://rairfoundation.com/bam-famous-doctor-exposes-fda-ivermectin-lies/;

republished below in full unedited for informational, educational & research purposes:

“Sadly, anything that might possibly work against the virus is opposed by those in power…” – TheBlaze Senior Editor Daniel Horowitz

Robert W. Malone, MD, the inventor of mRNA Vaccines, slammed the Food and Drug Administration (FDA) for discouraging the use of ivermectin as a potential treatment or prophylaxis for the coronavirus.

A viral Tweet from the FDA condescendingly portrayed Ivermectin only as a drug for animals, and therefore unacceptable for human consumption. “You are not a horse. You are not a cow. Seriously, y’all. Stop it,” read the Tweet, which linked to a completely unsourced article posted at the FDA’s website.

Dr. Malone took issue with the “childish” messaging from the FDA, stating in part that the message contradicts a current government-sponsored outpatient ivermectin clinical trial. Later, he tweeted an image of the ivermectin used for horses versus the ivermectin used for people.

“Ivermectin – one form is for horses, the other for humans. Simple stuff. Making it easy to understand. Is that sufficiently clear?” he said.

“The FDA has not reviewed data to support the use of ivermectin in COVID-19 patients to treat or to prevent COVID-19; however, some initial research is underway,” the article at the FDA website article concedes.

The move by the FDA is only the latest to discourage promising coronavirus treatments. As Dr. Joseph Mercola has stated:

“While the list of crimes committed by authorities during the COVID-19 pandemic is a long one, perhaps the biggest crime of all is the purposeful suppression of safe and effective treatments.”

TheBlaze Senior Editor Daniel Horowitz also took issue to the FDA’s obnoxious statement. “For the assholes at the FDA claiming ivermectin, which could save millions, is only for horses, here is the readout from the Nobel Prize Assembly on ivermectin,” he said.

Horowitz also linked to an article that goes into detail about how ivermectin has been beneficial for humans, not horses. “Sadly, anything that might possibly work against the virus is opposed by those in power,” Horowitz states in part.

Please see a newly-surfaced video clip of the chairman of the Tokyo Medical Association Haruo Ozaki praising ivermectin during a press conference on Feb. 9, 2021:

"...if we look at COVID numbers in countries that give ivermectin, the number of cases is 134.4 per 100,000, and the number of deaths is 2.2 per 100,000"

Source: https://biblescienceforum.com/2021/08/28/tokyos-medical-association-chairman-recommends-ivermectin/

Also: https://www.lifesitenews.com/news/breaking-japanese-medical-association-chairman-tells-doctors-to-prescribe-ivermectin-for-covid/

Fauci Set to Receive Biggest Federal Retirement Package in History

BY LUIS MIGUEL

SEE: https://thenewamerican.com/fauci-set-to-receive-biggest-federal-retirement-package-in-history/;

republished below in full unedited for informational, educational & research purposes:

Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases (NIAID) and the chief medical advisor to Joe Biden, is reportedly eligible for the largest federal retirement package in U.S. history. 

The 81-year-old has said he does not plan to retire soon. “There’s no way I’m going to walk away from this until we get this under control,” Fauci told ABC’s Johnathan Karl earlier this month. “I mean, that’s the purpose of what we do. That’s — that’s our mission in life. In the middle of it, I’m not going to walk away.” However, if he did retire, Forbes auditors at OpenTheBooks.com say that Fauci’s 55 years of service in the federal government qualify him for an annual retirement package of $350,000, which would go up through annual cost-of-living adjustments.

Moreover, Fauci is currently the federal government’s highest-paid employee, earning $434,321 in 2020 — a sum higher than that of the president, the military’s highest-ranking commanders, and the rest of the federal government’s 4.3 million employees.

The NIAID chief recently made headlines by suggesting that mandatory masks on airlines should continue into the indefinite future and voiced support for a vaccine requirement on domestic flights.

During his exchange with Karl, Fauci said, “We want to make sure people keep their masks on. I think the idea of taking masks off, in my mind, is really not something we should even be considering.”

He added, “Even though you have a good filtration system, I still believe that masks are a prudent thing to do and we should be doing it.”

Fauci went on to say that “A vaccine requirement for a person getting on the plane is just another level of getting people to have a mechanism that would spur them to get vaccinated; namely, you can’t get on a plane unless you’re vaccinated, which is just another one of the ways of getting requirements, whatever that might be. So I mean, anything that could get people more vaccinated would be welcome.”

Fauci has also been a proponent on Joe Biden’s vaccine employer mandate for companies. The Fifth Circuit Court of Appeals recently initially blocked the mandate, but the Sixth Circuit overruled that in a consolidated appeal.

As a result, a group of 47 Republican senators and 136 House members is asking the Supreme Court to block enforcement of the mandate

The brief by Republican lawmakers argues that under Biden, the Occupational Safety and Health Administration (OSHA) is acting outside the limits of its authority. They assert OSHA was created to protect workers from specific workplace hazards but never from viruses like COVID-19.

“The ETS provision of the OSH Act allows OSHA to address only ‘grave danger’ in the workplace, which includes any ‘toxic or physically harmful’ agent,” the brief reads. “In the statutory scheme established by Congress, these conditions are a meaningful restraint on the agency. OSHA, however, aggressively reads the restrictions as an opportunity for the agency to branch out into public healthcare policy.”

The New American recently reported that Fauci and the National Institutes of Health Director Francis Collins colluded to conduct a “quick and devastating” take-down of a document advocating for a lockdown-free COVID-19 response strategy.

Emails released last week by the House Select Subcommittee on the Coronavirus Crisis revealed retiring NIH Director Collins telling Fauci in October 2020 to discredit the Great Barrington Declaration (GBD) — an international document signed by nearly 900,000 physicians that warns against “the damaging physical and mental health impacts” of lockdowns and other forceful measures while calling for achieving herd immunity through “focused protection” of the most vulnerable.

In addition, reports have surfaced about Fauci doling out millions of dollars in National Institutes of Health (NIH) grants to the Wuhan Institute of Virology, from which COVID-19 escaped into the general Chinese public, starting the pandemic.

Per a report from Fox’s The Next Revolution With Steve Hilton, Fauci continued gain-of-function research even after an Obama administration ban, ultimately funding a China-based study that “unlocked a highly specific doorway into the human body.” That’s the same pathway used by COVID-19. According to the January 24 report, Fauci argued in a Washington Post article that “important information and insight can come from generating a potentially dangerous virus in the laboratory.”

FDA rolling back rules to allow doctors to send abortion pills though the mail as Post Office colludes with agency to intercept effective COVID med Ivermectin

Image: FDA rolling back rules to allow doctors to send abortion pills though the mail as Post Office colludes with agency to intercept effective COVID med Ivermectin

BY J.D. HEYES

SEE: https://www.naturalnews.com/2021-12-28-fda-to-allow-abortion-pills-though-mail-and-intercept-ivermectin.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) Once again, government agencies are working to deny Americans the freedom to choose while at the same time debasing what is left of our culture, in this case, the Food and Drug Administration appears to be working in tandem with the U.S. Postal Service.

The FDA announced last week that the agency is ditching existing regulations that prohibit properly licensed healthcare providers from sending women the first of a two-dose abortion pill, and, as some reports noted, the timing is extremely suspicious, per the American Wire:

Roughly two weeks after the high court heard oral arguments in a case involving a Mississippi law that essentially challenges Roe, the Food and Drug Administration has announced it is rolling back restrictions on sending abortion pills through the mail.

…[T]he  FDA permanently lifted restrictions on prescribers sending mifepristone, the first in a two-drug therapy that terminates pregnancies up to 10 weeks, through the mail.

Previously, FDA regulations required the pill to only be dispersed in clinics or hospitals by providers who were specifically certified to do so. 

Got that? The left-wing ghouls running the Biden regime seek to undermine a growing number of state laws that dramatically restrict abortions ahead of a Supreme Court decision that could wind up striking down the murderous procedure altogether or, at a minimum, return the 10th Amendment authority to states themselves for their residents to decide if they want to continue allowing the procedure or not and if so, under what conditions.

As a sop to the Democrat Party’s semi-sane faction, small though it may be, the FDA will not change the rules for misoprostol, which is the second drug in the treatment protocol and is taken up to 48 hours after the first one; it has already been available via prescription at any pharmacy for years.

“The FDA’s decision will come as a tremendous relief for countless abortion and miscarriage patients,” Georgeanne Usova, a lawyer with the American Civil Liberties Union, crowed (remember when this garbage ‘legal’ organization used to represent those who had no voice, regardless of their political positions — like the unborn, perhaps?). “However, it is disappointing that the FDA fell short of repealing all of its medically unnecessary restrictions on mifepristone and these remaining obstacles should also be lifted.”

“It’s really significant,” added Florida State University law professor Mary Ziegler, in response to the FDA’s rule change.

“Telehealth abortions are much easier for both providers and patients, and even in states that want to do it, there have been limits on how available it is,” she added.

Meanwhile, as the FDA allows doctors to send medication to a woman so she can kill her unborn child, the agency is working with the Post Office to prevent Americans from getting ivermectin, which has been proven to be effective against COVID-19, unlike a couple of the vaccines.

According to a press release from Customs and Border Protection (CBP), the seizure happened at the international mail facility within Chicago’s O’Hare International Airport on October 4, Newsweek reported.

The press release noted further that as officers were conducting an x-ray inspection of a package from China, they “noticed some discrepancies.” The package stated that it contained “decorative beads,” CBP said.

The outlet added:

Ivermectin, which is a drug often used in animals to combat parasites, has been praised by some as an effective treatment against COVID-19. The U.S. Food and Drug Administration (FDA) recently warned that Ivermectin is not an approved treatment against COVID-19 and can cause health issues in humans if used improperly.

“There are approved uses for ivermectin in people and animals but it is not approved for the prevention or treatment of COVID-19,” the FDA said on its website, adding that the drug is approved for human use to treat parasites, head lice, and “skin conditions such as rosacea.”

In fact, the FDA and the Post Office are specifically targeting ivermectin not China, as civil rights attorney Aaron Siri noted on Twitter this month.

“The FDA is working with the post office to hold packages containing ivermectin. The FDA could better use its resources to, I don’t know, publicly release the docs submitted by Pfizer to license its mandated liability-free V earlier than 75 years from now!” he wrote.

https://twitter.com/AaronSiriSG/status/1470182424797609984

Read more stories like this at Pandemic.news.

Sources include:

AmericanWireNews.com

BigLeaguePolitics.com

Newsweek.com

NaturalNews.com

MEDICAL FASCISM: FDA conspiring with USPS to block shipments of lifesaving ivermectin

Image: MEDICAL FASCISM: FDA conspiring with USPS to block shipments of lifesaving ivermectin

BY ETHAN HUFF

SEE: https://www.naturalnews.com/2021-12-17-fascist-fda-conspiring-usps-block-shipments-ivermectin.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) Attorney Aaron Siri published a document he discovered suggesting that the U.S. Food and Drug Administration (FDA) is conspiring with the United States Postal Service (USPS) to block imports of ivermectin being sent to American consumers from overseas.

In a tweet, Siri drew attention to a “Notice of FDA Action” letter explaining that the USPS is now illegally spying on packages. If found to contain ivermectin, those packages are being detained and later destroyed if the recipient is unable to prove that the shipment is for some other use besides treating the Tony Fauci Virus (Covid-19).

“A mail shipment addressed to you from a foreign country is being held by the post office at the request of the U.S. Food and Drug Administration (FDA),” the letter reads.

Listed below that sentence is a “Summary of Current Status of Individual Lines” showing a box of 200 tablets of Iverheal 12 Ivermectin Tablets USP 12mg, which the USPS detained on 11-09-2021.

“The shipment may also contain other items not listed above,” the letter goes on to read. “This notice does not constitute assurance the products involved comply with provisions of the Food, Drug, and Cosmetic Act (FD&CA), Public Health Service Act (PHSA), or other related acts, and does not preclude action should the products later be found violative.”

The FDA wants people to die without ivermectin

The recipient was then told that an “examination” of the package’s contents led the FDA to determine that the drugs “are not in compliance with the requirements of the law.”

“Additionally, FDA has determined that each article is valued at $2500 or less,” it further explains. “Because these drugs are not in compliance with the requirements of the law and are valued at $2500 or less, they are subject to refusal of admission into the United States and are subject to administrative destruction.”

According to the FDA, any use of ivermectin in the age of the Fauci Flu represents “misbranding” and will not be allowed. The only drugs accessible to people now are the “vaccines” from Operation Warp Speed.

“The imported drug does not appear to comply or meet the exemption considerations under the FDA personal importation policy,” the letter adds.

The letter does explain that the recipient can challenge the package’s interception and attempt to retrieve it by making a case in favor of its proper receipt. If this is not done within a certain period of time, then the FDA and the USPS plan to destroy the ivermectin pills. (RELATED: Ivermectin is a powerful weapon against the Chinese Flu, which is why the FDA does not want you to have it).

“While no response is required, if you decide to respond, please submit evidence to overcome the appearance of the violation to my email address (below) and include your name and entry number in the subject heading,” the letter goes on to instruct.

Siri pointed out that the FDA could use its resources much more wisely than this and leave people be to use the interventions they wish to stay safe against Fauci Germs. Instead, the FDA appears to want more people to die by restricting access to ivermectin.

“The FDA could better use its resources to, I don’t know, publicly release the docs submitted by Pfizer to license its mandated liability-free V (vaccine) earlier than 75 years from now!” Siri tweeted, intentionally using “V” to describe the vaccine to avoid being censored on the social media platform.

“So they really ARE murdering us,” someone responded to Siri’s tweet.

More related news about the FDA, the USPS and the Fauci Virus can be found at Fascism.news.

Sources for this article include:

Sirillp.com

Twitter.com

NaturalNews.com

Smoking gun confidential Pfizer document exposes FDA criminal cover-up of VACCINE DEATHS… they knew the jab was killing people in early 2021… three times more WOMEN than MEN

BY MIKE ADAMS

SEE: https://www.naturalnews.com/2021-12-02-smoking-gun-pfizer-document-exposes-fda-criminal-cover-up-of-vaccine-deaths.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) Thanks to the efforts of a group called Public Health and Medical Professionals for Transparency, we now have smoking gun confidential documents that show Pfizer and the FDA knew in early 2021 that pfizer’s mRNA vaccines were killing thousands of people and causing spontaneous abortions while damaging three times more women than men.

One confidential document, in particular, was part of a court-ordered release of FDA files that the FDA fought by claiming the agency should have 55 years to release this information. A court judge disagreed and ordered the release of 500 documents per month, and the very first batch of documents contained this bombshell entitled, “Cumulative Analysis of Post-Authorization Adverse Event Reports.”

Get it here:

https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf

Or here, mirrored on NN servers:

https://www.naturalnews.com/files/536-postmarketing-experience.pdf

The document reveals that within just 90 days after the EUA release of Pfizer’s mRNA vaccine, the company was already aware of voluntary adverse reaction reports that revealed 1,223 deaths and over 42,000 adverse reports describing a total of 158,893 adverse reactions. The reports originated from numerous countries, including the United States, United Kingdom, Italy, Germany, France, Portugal, Spain and other nations.

Aside from “general disorders,” the No. 1 most frequently reported category of mRNA vaccine adverse reactions was Nervous system disorders, clocking in at 25,957 reports.

Pfizer has withheld the total number of doses released across the world, citing corporate trade secrets. This is indicated by “(b) (4)” in the document, where specific numbers and facts are redacted.

Even these numbers — already quite shocking, given the FDA’s insistence that mRNA vaccines are “safe and effective” — barely scratch the surface of the damage and deaths caused by these vaccines. “Reports are submitted voluntarily, and the magnitude of underreporting is unknown,” says Pfizer on page 5.

Three times as many women damaged, compared to men

Shockingly, the document reveals that more than three times as many women were damaged by the Pfizer vaccine, compared to men. There were 29,914 adverse events recorded in women, with just 9,182 recorded in men. It is not known whether the same number of men and women took the vaccine, but this number exposes the very real possibility of a gender-specific vaccine damage risk that the FDA went to great lengths to cover up.

Anecdotally, most of the neurological damage we’ve seen in people who have been damaged by the vaccine — convulsions, numbness, pain, etc. — has been depicted in women, not men. It looks like the FDA knows the mRNA vaccine exhibits a disproportionate, gender-specific damage profile that also affects women in terms of spontaneous abortions (also covered in the report).

Pfizer told the FDA its mRNA covid vaccines can cause “enhanced disease” by making covid worse

Also to the shock of many observers who are just now digging into this smoking gun document, Pfizer told the FDA under “Safety concerns” (section 3.1.2) that its mRNA injection could cause, “Vaccine-Associated Enhanced Disease (VAED), including Vaccine-associated Enhanced Respiratory Disease (VAERD).”

This means the FDA knew the vaccine could sicken and kill patients who were later infected with covid.

Under the label of “missing information,” Pfizer also told the FDA that it has no information about “Use in Pregnancy and lactation” nor covering “Use in Paediatric Individuals < 12 Years of Age.”

“Vaccine Effectiveness” was also listed as “Missing information” by Pfizer.

In other words, Pfizer told the FDA its vaccines could kill people and that it had no information about vaccine effectiveness, yet the FDA fraudulently pushed the vaccine as “safe and effective” anyway. Pfizer even told the FDA that it had no safety information about use in pregnant women, yet the FDA (and Fauci, the CDC, etc.) all pushed the vaccine for pregnant women, despite the utter lack of safety information.

Based on this document, it appears that the FDA itself has been neck-deep in a criminal conspiracy to hide the truth about vaccine injuries and deaths while granting usage approvals to the very same corporations that openly told the FDA its products were killing people.

Note, too, that the entire corporate media complex has lied from day one, falsely claiming the vaccine has killed no one. They are, of course, complicit in this vaccine holocaust.

Spontaneous abortions, neonatal death, and other effects on pregnant women

In the section labeled, “Use in Pregnancy and lactation,” the report discusses reports of the mRNA vaccine being linked to:

spontaneous abortion (23), outcome pending (5), premature birth with neonatal death, spontaneous abortion with intrauterine death (2 each), spontaneous abortion with neonatal death, and normal outcome (1 each).

Notice that “spontaneous abortion” represents by far the highest number in these reports. In other words, the FDA knew this vaccine would kill unborn babies, but they pushed it on pregnant women anyway.

All mRNA vaccines must be immediately halted, and FDA bureaucrats must be indicted and arrested

This confidential document — just the first of thousands yet to be released — reveals two critical things:

1) The FDA committed criminal fraud and misrepresentation in approving mRNA vaccines as “safe and effective.” This means top FDA decision-makers must now face arrest and criminal prosecution.

2) The mRNA vaccine was known by Pfizer to be deadly even in its first three months of emergency use. This means Pfizer is also complicit in the continued deaths of innocent victims, as Pfizer itself should have pulled its deadly vaccine and halted all sales and distribution.

Find even more details in today’s Situation Update podcast which also covers Alex Baldwin’s magic gun, left-wing abortion pill gobblers protesting SCOTUS, Dr. Oz. running for the US Senate, Australia’s covid death camps, and much more:

Brighteon.com/6779b557-d912-4ff9-8191-06e7ff6aae03

Discover a new podcast each day, along with interviews, special reports, and documentaries, at the HR Report channel on Brighteon:

https://www.brighteon.com/channels/hrreport

Whistleblower says Pfizer “falsified data,” conducted flawed covid “vaccine” trials to rig FDA approval

BY ETHAN HUFF

SEE: https://www.naturalnews.com/2021-11-03-whistleblower-pfizer-falsified-data-flawed-covid-trials.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) A drug industry whistleblower has come forward with leaked evidence showing that Pfizer falsified data, broke fundamental rules and delayed reporting adverse reactions in its Wuhan coronavirus (Covid-19) “vaccine” trials.

Brooke Jackson, who was recently fired from her position as regional director at the Ventavia Research Group, a Pfizer contract partner, told the British Medical Journal (BMJ) that multiple trials at several research sites in Texas produced flawed results based on these poor practices.

Not only was Pfizer “slow” to report problems during the trials, but it also unblinded patients, hired on inadequately trained vaccinators, and cut corners to produce desired results rather than accurate results.

Jackson says that staff members who were involved in quality control checks became overwhelmed at the sheer volume of problems that arose because of the company’s tampering with the normal standards for trials of this type.

Concerned about everything she was witnessing, Jackson tried to approach her superiors about it. She also emailed a complaint to the U.S. Food and Drug Administration (FDA) before being promptly fired that same day.

After this occurred, Jackson proceeded to send a trove of incriminating evidence to the BMJ, including internal company documents, photos, audio recordings and emails.

“One photo … showed needles discarded in a plastic biohazard bag instead of a sharps container box,” reports indicate. “Another showed vaccine packaging materials with trial participants’ identification numbers written on them left out in the open, potentially unblinding participants.”

Rather than take her concerns seriously when presented with the facts, Ventavia instead questioned Jackson for taking photos of the incriminating evidence.

FDA always sides with Big Pharma, not We the People

Another problem Jackson revealed about the Pfizer contract company’s trial protocols involved data entry, which was not properly maintained throughout the process.

The expectation was that all queries would be addressed within 24 hours, however there were more than 100 of them older than that, a later investigation revealed.

“Subject has reported with Severe symptoms/reactions … Per protocol, subjects experiencing Grade 3 local reactions should be contacted,” one query for two separate individuals read.

“Please confirm if an UNPLANNED CONTACT was made and update the corresponding form as appropriate.”

Upon receipt of this query, investigators should have made phone contact “to ascertain further details and determine whether a site visit is clinically indicated.” Instead, nothing was done.

At least three employees at Ventavia were also identified by company executives as problematic due to suspicions that they were involved with falsifying data. One of these employees was reportedly “verbally counseled for changing data and not noting late entry.”

The FDA, it was feared, might come in to conduct an audit, which apparently petrified Ventavia because it knew its protocols were not up to proper standards.

“People working in clinical research are terrified of FDA audits,” stated someone named Jill Fisher who is involved with all this. “I don’t know why they’re so afraid of them … You would think if there’s a specific and credible complaint that they would have to investigate that.”

Other problems outlined by Jackson include:

• Trial participants placed in a hallway post-injection without any monitoring by clinical staff
• Lack of timely follow-up of participants who experienced adverse events
• Deviations from protocol not being reported
• Injection vials not being stored at proper temperatures
• Mislabeled laboratory specimens
• Staff members being targeted by Ventavia for bringing up issues and problems

Jackson was told by the FDA in response to her complaints that no comment would be provided. It was later discovered that the FDA looked into just nine of the trial’s 153 sites, and not a single one involving Ventavia was investigated.

The latest news about Chinese Virus injections can be found at ChemicalViolence.com.

Sources for this article include:

ZeroHedge.com

NaturalNews.com

DR. JOHN BERGMAN: Pharmaceutical Control of Your Lives

With the world becoming increasingly toxic and the incredible lack of knowledge regarding appropriate healthcare, it has never been more important to take charge of your health and your life. The Extreme Health Academy is a website that's full of information to help you learn exactly what you must do to survive and thrive in this world. Best of all this website is a community of people ready to help others on the road to optimal health with features like an online forum, live workshop, podcasts, monthly video courses a supporting community, and much more!

IT GETS WORSE: Fauci funded inhumane medical experimentation on minority AIDS orphans in NYC

Image: IT GETS WORSE: Fauci funded inhumane medical experimentation on minority AIDS orphans in NYC

BY ETHAN HUFF

SEE: https://www.naturalnews.com/2021-10-28-fauci-funded-inhumane-medical-experimentation-aids-orphans.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) After it was revealed that Tony Fauci sent American taxpayer dollars to an animal abuse operation that tortured and murdered dogs, it has since come to light that Fauci did much the same thing to human AIDS orphans in New York City back in the early 2000s as well.

Circulating photos include one depicting a young black boy being experimented on at a NYC hospital. The boy shown was one of hundreds that Fauci exploited as part of a Tuskegee-style government-Big Pharma experiment that led to at least 25 minor deaths during the study, another 55 deaths after the fact in foster care, and hundreds more deaths after that.

“In 2005, the city of New York hired the VERA Institute to form a final report on the drug trials,” it was reported. “VERA was given no access to medical records for any of the children used in trials. Their report was published in 2008.”

“They reported that twenty-five children died during the drug studies, that an additional fifty-five children died following the studies (in foster care), and, according to Tim Ross, Director of the Child Welfare program at VERA (as of 2009), 29% of the remaining 417 children who were used in drug studies had died (out of a total 532 children that are admitted to have been used).”

Nobody likes Fauci except the mainstream media

As always, no payment or compensation was given to any of the children who were used in the trials, nor to their parents. They were mere fodder for Fauci’s mad scientist “research,” which continues to this very day as no president has yet had the guts or gall to get rid of him.

Fortunately, there are brave souls not in government who are coming forward to tell all about what the National Institute of Health (NIH) has been doing for decades, committing serious crimes against humanity.

The following video features an Incarnation Children’s Center (ICC) interview between Liz Brown and Mimi Pascual that talks all about this in greater depth. It starts around the 24:30 mark where key points of the interview occur:

Numerous documents and interviews with children and childcare workers at ICC who participated in the Fauci-funded research are speaking out about the horrors they witnessed and contributed to, not realizing fully what they were doing until the damaging effects and deaths appeared after it was completed.

Fauci, of course, more than likely knew fully about the risks involved. To him, though, human life is meaningless. Its only worth is to be experimented on for “research” purposes.

Back then, only a few hundred children were affected by Fauci’s mad scientism. Today, the entire world is being injected with experimental poisons, the full effects of which have yet to fully manifest.

“Dr. Fauci is Dr. Frankenstein and Dr. Moreau into one,” joked one commenter at The Gateway Pundit.

“More like Dr. Mengele,” responded another.

“One might ask … ‘Why now? Why is Fauci being exposed and incriminated now?'” speculated another. “Could it be he is no longer a trusted and valuable tool for the cabal in power?”

“This … ‘man’ … has been scum since the introduction of HIV back in the ’80s. The disease was politicized back then … and oh! Lookie here … this ‘new’ ‘not-gain-of-function-disease’ … that he has had a direct hand in … has been … politicized, too …”

Another called out National Geographic for launching a ridiculous “documentary” portraying Fauci as some kind of hero for humanity rather than the demented monster that he truly is.

“This is all coming back to light because this is one of the reasons that black people in New York City refuse to take the jab,” noted another.

More of the latest news about Fauci can be found at Evil.news.

Sources for this article include:

NaturalNews.com

TheGatewayPundit.com

FDA declares biological war on children with “final sacrifice” of the innocent

IF NOT ANIMAL CRUELTY, THEN CHILD CRUELTY

OAN: Stephanie Hamill w/ D.C. Draino

PETA CALLS FOR FIRING OF FAUCI FROM NIH

OAN: Animal Cruelty Scandal with Anthony Bellotti

Rumble — Anthony Bellotti, founder, and president of White Coast Waste Project gives The Real Story on Anthony Fauci’s animal cruelty labs.

BY ETHAN HUFF

SEE: https://www.naturalnews.com/2021-10-28-fda-biological-war-children-final-sacrifice-innocent.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) In a unanimous vote of 17-0, the U.S. Food and Drug Administration’s (FDA) vaccine advisory panel has recommended that the agency officially authorize the “emergency” use of Pfizer-BioNTech’s Wuhan coronavirus (Covid-19) “vaccine” in children ages five through 11.

The FDA does not have to abide by this recommendation, but chances are that it will because there really has never been a chemical injection that the agency has not wanted to stab into people’s arms, no matter how dangerous.

In fact, the FDA works overtime to get dangerous and ineffective vaccines approved. When they injure and kill children, the FDA covers it all up and pretends as though nothing is wrong.

If or when the FDA approves the Pfizer-BioNTech injection for children as young as five, the U.S. Centers for Disease Control and Prevention (CDC) will then issue an opinion of its own about the matter.

According to reports, children between five and 11 years of age would receive a modified injection that contains only one-third the amount of vaccine per dose. Children 12 years of age and older will continue to receive the full doses.

FDA voting member says he had to vote in favor of covid vaccination for little kids in order to find out what it does to them

When asked why he voted in favor of the recommendation, one of the FDA advisory members revealed that “we’re never going to learn about how safe the vaccine is until we start giving it.”

In other words, nobody really knows what these things are going to do to society’s youngest members, and the only way to find out is to start experimentally injecting them with mRNA spike protein vials.

This is a similar rationale to the one once given by political dinosaur Nancy Pelosi when asked why she voted in favor of passing Obamacare. Since nobody actually read the legislation, Pelosi infamously stated that Congress had to pass it in order to find out what was in it.

By recommending that young children get jabbed with experimental Big Pharma chemicals that will permanently alter their DNA and leave them with damaged immunity, the FDA vaccine advisory panel is waging a biological war against our nation’s youth.

It would seem as though this could be the American government’s last abominable move before God Almighty himself intervenes to protect his innocent creation from being genetically butchered by Tony Fauci and his fellow death worshippers who would love for nothing more than to inject every last human soul with their chemical poisons.

This whole thing really does seem like some kind of ritual child sacrifice to the Branch Covidian god, who appears to demand the blood of innocents in order to quell his fury. The more children whose parents agree to get them jabbed, the happier their god is, which means fewer other “covid” restrictions such as lockdowns and mask mandates.

“All 17 board members who voted to approve this need to hang,” wrote one commenter at Zero Hedge, noting that the “study” they used to justify their yes votes was only two months long and proved absolutely nothing based on how it was constructed.

“This is meaningless statistical noise, also known as lying with statistics,” this same commenter added.

“The study isn’t large enough to detect any extremely rare side effects, such as the heart inflammation that occasionally occurs after the second dose, mostly in young men and teen boys,” the study itself further revealed its major shortcomings.

The government wants Chinese Virus injections to be repeatedly stabbed into everyone’s arms probably until the end of time. To keep up with the latest, visit ChemicalViolence.com.

Sources for this article include:

ZeroHedge.com

NaturalNews.com

__________________________________________________________________

FDA: "We're Never Going to Learn About How Safe the Vaccine for Children Is Until We Start Giving It"

BY VERONIKA KYRYLENKO

SEE: https://thenewamerican.com/fda-were-never-going-to-learn-about-how-safe-the-vaccine-for-children-is-until-we-start-giving-it/;

republished below in full unedited for informational, educational & research purposes:

The Food and Drug Administration’s Vaccines and Related Biological Products Advisory Committee met on Tuesday to discuss Pfizer-BioNTech COVID-19 vaccine for children five through 11 years of age (full recording is available here).

While the committee endorsed the shot in a 17-0 vote, one FDA panelist, Dr. Eric Rubin, made some unsettling remarks in regard to vaccines’ safety, saying, verbatim, “We’re never gonna learn about how safe the vaccine is until we start giving it. That’s the way it goes.”

Dr. Rubin noted,

This is a much tougher one, I think, than we had expected coming into it. The data show that this vaccine works and it’s pretty safe.… And yet, we’re worried about a side effect that we can’t measure yet, but it’s probably realAnd we see a benefit that isn’t the same as it is in older patients.

Dr. Rubin further stated:

It’s a very, sort of, personal choice. If I had a child who was a transplant recipient, I would really want to be able to use a vaccine. And there are certain kids who probably should be vaccinated. The question of how broadly to use I think is a substantial one. And I know it’s not a question, and I know we’re kind of punting that to ACIP [Advisory Committee on Immunization Practices of the CDC].

But I do think that it’s a relatively close call…. It really is going to be a question of what the prevailing conditions are. But we’re never going to learn about how safe this vaccine is unless we start giving it. That’s just the way it goes. That’s how we found out about rare complications of other vaccines like coronavirus vaccine. And I do think we should vote to approve it.

Dr. Rubin did not argue that the committee should issue a limited endorsement for the jab, and recommend it only to immunocompromised children or those having known co-morbidities to COVID, such as obesity or diabetes. While admitting that the benefits of vaccination for young children are not as great compared to those in older people and that the long-term safety will only be learned after the vaccination begins, he still fully endorsed it.

The mainstream media was quick to try to sugar-coat Rubin’s statement.

Aaron Blake of the Washington Post wrote that Dr. Rubin’s comment was “significant and noteworthy,” but, at the same time, it was “basically tailor-made for vaccine skeptics such as Tucker Carlson and Sen. Ron Johnson (R-Wis.).”

The outlet “explained” that the parents should not worry, because they are not being “forced” to inoculate their children with experimental jab yet.

What the FDA is considering here, after all, is not forcing any children ages 5 to 11 to take the vaccine; rather, it’s about giving parents the option,” the article reads. The parents must understand that in the situation of a “public health emergency … difficult decisions need to be made without the kind of extensive studies everyone would prefer were done.”

In other words, while the long-term side effects in children are not yet fully studied, and there is no knowledge of the “rare” side effects, the parents should “trust the science” and at this time decide for themselves whether they want their kids jabbed. Blake, while seemingly seeing no problem with the idea of forcing people to take a drug against their will, added that no “forcing” will even begin “until we get the more extensive data.”

This type of “reassurance” is troubling since we have already seen that the FDA and the CDC are uninterested in analyzing their own data on possible side effects associated with COVID vaccines in adults. VAERS, an admittedly “passive” system that only reflects a “tiny fraction” of all adverse reactions, has already recorded some 16,310 deaths (with 5,326 of those deaths occurring within two days following the vaccination), and 778,685 total adverse events to COVID jabs, yet the top regulatory and health agencies continue to insist the vaccines are “safe.” Moreover, the Biden administration is employing increasingly coercive tactics to get people inoculated.

Dr. Rubin was not the only speaker who conveyed some troubling messages.

Dr. Fiona Havers of the CDC admitted there are no studies on the long-term outcomes of the vaccine in children (1:03:22), as there is no information available on the vaccinated children’s chances of reinfection (1:05:44).

Dr. Matthew Oster, a pediatric cardiologist, commenting on the data available on vaccinated adolescents, outlined the higher chances of young male vaccine recipients having higher chances of developing heart inflammation than their unvaccinated peers (1:11:26). In females, the risk of developing myocarditis following vaccination was lower than in males, yet still exceeded the “background incidence.” At the same time, the chances of adolescents developing myocarditis due to COVID were significantly lower compared to them developing the condition due to vaccination (1:20:13).

As of October 21, COVID-19 death rate in children ages 5-11 represented 0.03 percent of all COVID-19 deaths in the United States, 0.008 percent of total COVID-19 cases, and 0.0005 percent of deaths among the entire U.S. population. The age group of 0-17 years made up for 0.0000002 percent deaths by total COVID-19 cases, according to the CDC data that was presented during the discussion (4:43:49).

The safety data on the Pfizer shot for children, based on “at least two months of follow-ups,” showed, according to the FDA (2:20:01), that no recipients developed any of the “adverse events of special interest,” including myocarditis/pericarditis, anaphylaxis, Bell’s palsy, and appendicitis.

FDA endorses murderous vaccine ATROCITIES against children~Emergency Rooms across America being filled with post-vaccine patients suffering serious illness

BY MIKE ADAMS

SEE: https://www.naturalnews.com/2021-10-27-fda-endorses-murderous-vaccine-atrocities-against-children.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) In a 17-0 decision, an FDA committee has codified medical atrocities against innocent children across America by voting to approve “emergency use” of covid vaccines in children aged 5 – 11.

Importantly, there is no medical need for children aged 5 – 11 to take covid vaccines at all, given that their mortality rate from covid infections is nearly zero.

Because of the near-zero mortality rate, there is no “benefit” that can be offered by the vaccines. Only risks. And these vaccines are incredibly risky, having already killed an estimated 250,000 Americans so far (and counting). Source: Dr. Zev Zelenko.

This means the FDA panel members, by approving this deadly vaccine for children, are carrying out medical genocide against innocent children on a scale never even imagined by Third Reich medical experiments doctor Josef Mengele.

The White House now plans to assault 28 million children with vaccine violence, and the mass slaughter of innocents is being carried out like clockwork. The only question remains: Will the slaughter of innocent children finally be enough to awaken America to the genocidal evil of Big Pharma and its captured regulators like the FDA?

Find more answers in today’s Situation Update podcast below…

NPR admits emergency rooms across America are “swamped” with organ failures and serious illness… it looks like a wave of vaccine injuries

As we’ve documented numerous times, covid vaccines destroy the innate immune system. This is part of their functional design, for if they didn’t suppress immunity, the vaccine’s mRNA strands would be attacked and destroyed by the immune system before they could infect human cells and take over the protein synthesis of ribosomes.

Current estimates show that people who have taken mRNA-based covid vaccines (Moderna and Pfizer) lose about 5% of their innate immune function each week. After about 20 weeks, they are characterized as “AIDS patients” who have little to no functioning immunity against in-the-wild pathogens such as common colds and flu viruses.

Beyond merely theoretical, this phenomenon is now being confirmed by the swamping of US hospital emergency rooms with post-vaccine patients who are exhibiting extreme levels of sickness against common health insults. “ERs are now swamped with seriously ill patients — but many don’t even have COVID,” reported NPR.org yesterday. Running out of ER rooms, patients are being treated in reclining chairs placed in hallways. From the NPR story: (emphasis added)

Months of treatment delays have exacerbated chronic conditions and worsened symptoms. Doctors and nurses say the severity of illness ranges widely and includes abdominal pain, respiratory problems, blood clots, heart conditions and suicide attempts, among others.

A separate section of the hospital was turned into an overflow unit. Stretchers stack up in halls. The hospital has even brought in a row of brown reclining chairs, lined up against a wall, for patients who aren’t sick enough for a stretcher but are too sick to stay in the main waiting room.

There is no privacy, as Alejoz Perrientoz just learned. He came to the ER this particular morning because his arm has been tingling and painful for over a week now. He can no longer hold a cup of coffee. A nurse gave him a full physical exam in the brown recliner, which made him self-conscious about having his shirt lifted up in front of strangers. “I felt a little uncomfortable,” he whispers. “But I have no choice, you know? I’m in the hallway. There are no rooms.”

[Notice that the tingling arm is a typical consequence stemming from vaccine injury and blood clots…]

“We are hearing from members in every part of the country,” says Dr. Lisa Moreno, president of the American Academy of Emergency Medicine (AAEM). “The Midwest, the South, the Northeast, the West … they are seeing this exact same phenomenon.”

NPR, of course, utterly fails to link any of this with vaccines, even when patients are being diagnosed with blood clots, heart conditions, breathing difficulty, and the tingling of extremities. These are all vaccine side effects, yet no one in the media will dare report that truth.

The upshot is that emergency rooms are being overrun with vaccine-injured patients… and it’s not even November yet. Imagine what the scene looks like in mid-January.

This is one of those “we told ya so” moments, it seems when the vaccine zealots realize they’re already dead because they foolishly believed a depopulation weapon system was a beneficial vaccine. Without question, millions of vaccinated Americans will be dead or health compromised before Spring. What we’re seeing now is just the leading edge of the health care catastrophe yet to be fully realized.

Find more details in today’s Situation Update podcast here:

Brighteon.com/0b12e476-5181-40f9-b43d-47b92e766296

“Do Not Stand Idly by While Your Neighbor’s Blood Is Shed”: Israeli Docs Warn FDA of Pfizer Shots’ Risks

BY VERONIKA KYRYLENKO

SEE: https://thenewamerican.com/do-not-stand-idly-by-while-your-neighbors-blood-is-shed-israeli-docs-warn-fda-of-pfizer-shots-risks/;

republished below in full unedited for informational, educational & research purposes:

Professional Ethics Front, an independent Israeli group of physicians, lawyers, scientists, and researchers has expressed its “severe concerns” regarding the reliability and legality of official Israeli COVID vaccine data to the U.S. Food and Drug Administration (FDA), which is set to decide on recommending administering Pfizer vaccines to U.S. children ages 5-11.

The FDA relies heavily on data from Israel, which unrolled the world’s fastest vaccination campaign with 65 percent of the population being fully vaccinated as of October 23 and just under four million eligible Israelis having already taken a third dose in a country of nine million people.

While Israeli health authorities have not yet approved the Pfizer shot for children ages 5-11, Professional Ethics Front noted in its letter that “Israel is perceived as ‘the world laboratory’ regarding the safety and efficacy of the Pfizer-BioNTech COVID-19 vaccine.”

The group further acknowledged the fact that “the data and information coming from Israel play a crucial role in critical decision-making processes in regards to COVID-19 vaccination policies,” while stating the data is “flawed,” and its collection is accomplished by “significant legal and ethical violations.”

The letter outlines what it describes as “the main failures” of Israel’s data and reporting.

1. Lack of a Public and Transparent Adverse Events (AE) Reporting System

Israel does not have a “proper and transparent” system that tracks AEs associated with the vaccines, the letter states, adding that “healthcare professionals or citizens in Israel, who wish to submit reports of AEs following vaccination, are unable to do so.”

While the Ministry of Health (MOH) has an online AE reporting form available, this form “was for many months not useful since it did not allow the inclusion of personal contact information.” In addition to that, the free text field intended to describe the AEs allowed users to enter a limited number of characters, which means detailed reports could not be submitted. Finally, the symptoms list available to choose from was also very limited and included only mild AEs.

While the system was later fixed and the list was expanded, “the modification of the form was made very late after the majority of the adult population had already been vaccinated,” the group complains.

Such critical information as the AEs that occur in the “most vulnerable populations” such as pregnant women and seniors are not being tracked at all, per the letter.

2. Severe Obstacles to Reporting Adverse Events

The physicians and medical teams encounter “great obstacles” when attempting to report AEs associated with the jabs.

Citing the numerous testimonies of healthcare practitioners, the letter states that there is an “immense underreporting of AEs” which are “only rarely reported in exceptional cases.”

The letter alleges the MOH dismisses almost all reports on severe adverse events such as heart inflammation in young vaccine recipients.

3. Data Distortion

The MOH seems to deliberately try to avoid any public discussion on the jabs’ safety. Recently, MOH is alleged to have deleted “thousands” of citizens’ critical responses to a post entitled “Let’s talk about the adverse events,” claiming that the vaccine is “completely safe” and that severe AEs are “extremely rare.”

The MOH is also accused of misleading the public on the effectiveness of Pfizer’s third dose, which turned out to be much lower than was previously claimed.

4. Legal and Ethical Violations in Data-collection Processes

The signatories state that the Pfizer shots are administered to Israelis without their informed consent, which is “a clear violation of the Nuremberg Code Rules, the Patient’s Bill of Rights, and the Israeli MOH directives for clinical trials on humans.” At the same time, “the Israeli citizens are under tremendous pressure to get vaccinated, almost to the point of coercion.” Indeed, on June 22, prime minister Naftali Bennett announced those failing to present proof of vaccination or negative COVID tests would be barred entry from places such as movie theaters, sports games, amusement parks, synagogues, or activities attended by 100 or more people.

In September, Israeli Health Minister Nitzan Horowitz warned that the government might cancel the so-called Green Pass of people not inoculated with three doses of the coronavirus vaccine.

The Professional Ethics Front’s letter closes with a quote from the Torah:

In the Book of Leviticus, it is said “Do not stand idly by while your neighbor’s blood is shed”. In the spirit of those words, we implore the committee to take into consideration our urgent warnings and adopt utmost precaution when referring to the Israeli data concerning the safety and efficacy of the Pfizer-BioNtech COVID-19 vaccines.”

The FDA’s Vaccines and Related Biological Products Advisory Committee is meeting on Tuesday to discuss a request to amend Pfizer-BioNTech’s Emergency Use Authorization (EUA) for administration of their shot to children five through 11 years of age. 

On Friday, the FDA posted a briefing document claiming that the Pfizer vaccine’s benefits in preventing hospitalizations and deaths “would clearly outweigh” any serious side effects in children.    

If the FDA decides the shot is “safe and effective” for children, the CDC’s Advisory Committee of Immunization Practices would recommend its use on November 2-3.

On October 20, the Biden administration announced it has already acquired enough Pfizer child-sized doses to inoculate the nation’s 28 million children and is setting up all the necessary infrastructure to achieve that.

Dr. Dog Torturer: Fauci funds barbaric torture of beagles in a Tunisian lab

HORRENDOUS Testing on Puppies Paid for by Dr Fauci's NIH, with YOUR Tax Dollars

WCW exposes Fauci’s NIH sent $375K to Africa for beagles to be eaten alive. 

White Coat Waste Project VP Justin Goodman talks about WCW's latest exposé of Fauci's NIAID sending tax dollars to Tunisia for cruel dog experiments. Learn more: https://blog.whitecoatwaste.org/2021/...

Fauci ROASTED Over BARBARIC NIH-Funded Puppy Testing, Glenn Greenwald Reveals YEARS Of Experiments

PETA VP calls for Dr. Fauci's resignation after puppy experiments report

On Monday's "American Agenda", PETA senior VP Kathy Guillermo discussed reports of experimentation on puppies funded by the NIH.

White Coat Waste Project has exposed FOUR different locations where #Fauci funded wasteful & brutal BEAGLE experiments. Georgia, California, Africa… even Fauci’s own NIH lab in Maryland! What could be next? #BeagleGate

'Flat-Out Disgusting': Florida Governor DeSantis Tears Into Fauci Over Experiments On Dogs

BY LLOYD BILLINGSLEY

SEE: https://www.frontpagemag.com/fpm/2021/10/dr-anthony-fauci-funds-torture-beagles-tunisian-lloyd-billingsley/;

republished below in full unedited for informational, educational & research purposes:

“Our investigators show that Fauci’s NIH division shipped part of a $375,800 grant to a lab in Tunisia to drug beagles and lock their heads in mesh cages filled with hungry sand flies so that the insects could eat them alive,” the non-profit White Coat Waste project told reporters. “They also locked beagles alone in cages in the desert overnight for nine consecutive nights to use them as bait to attract infectious sand flies,” all to test an “experimental drug.”

White Coat Waste also claimed that some of the dogs had their vocal cords removed so their barking would not disturb the attending scientists. Rep. Nancy Mace fired off a letter to the National Institutes of Health, calling the cordectomies “cruel” and a “reprehensible misuse of taxpayer funds.” Mace is a South Carolina Republican but signatories to her letter included Democrats Cindy Axne, Steve Cohen, Jimmy Gomez, Josh Gottheimer, Ted Lieu, Mike Quigley, Lucille Roybal-Allard, Terri Sewell and Eleanor Holmes Norton, plus more than a dozen Republicans, including Reps. Brian Fitzpatrick and Maria Salazar.

In a related cause that could use more bipartisan support, Dr. Fauci and his National Institute of Allergy and Infectious Diseases (NIAID) are also under fire for funding dangerous gain-of-function research at the Wuhan Institute of Virology in China. The NIAID boss denied funding such research, but now the NIH admits a “limited experiment” to test if bat coronaviruses were “capable of binding” to a human receptor. That contradicts Fauci, the nation’s chief white coat supremacist, who has escaped scrutiny on a number of fronts.

Fauci earned a medical degree in 1966 but to avoid treating American soldiers in Vietnam, he hired on with the NIH in 1968 as one of their “yellow berets.” Fauci’s bio shows no advanced degrees in molecular biology or biochemistry, but in 1984 he became director of NIAID. Kary Mullis, who earned a PhD in biochemistry from UC Berkeley and won a Nobel prize for the polymerase chain reaction (PCR), called Fauci unqualified for the job.

“He doesn’t understand electron microscopy and he doesn’t understand medicine,” Mullis said. “He should not be in a position like he’s in.”

As UC Berkeley molecular biologist Peter Duesberg noted in Inventing the AIDS Virus,  Fauci networked with pharmaceutic giant Burroughs Wellcome and recommended azidothymidine, also known as AZT. The drug is marketed under the names Zidovudine or Retrovir, even though it “amounts to poison” according to Duesberg.

In 1989, Fauci’s NIAID conducted trials of AZT on pregnant mothers injected with HIV. As Duesberg noted, “A drug that interferes with growth can lead only to physical deformities in babies developing in the womb.” See also Poison by Prescription: the AZT Story by John Lauritsen, with a foreword by Duesberg, and this interview with former Harvard and Johns Hopkins molecular biologist Charles Thomas.  

When Duesberg challenged the government orthodoxy on AIDS, Fauci contrived to cancel his media appearances and the Berkeley virologist found his grants under attack. Fauci was hopelessly wrong about the spread of AIDS in the general population, yet he remained at the helm of NIAID.

In 2012, Fauci cited the risks of gain-of-function research, which makes viruses more lethal and transmissible, wondering, “what if that scientist becomes infected with the virus, which leads to an outbreak and ultimately triggers a pandemic?” The NIH banned gain of function research in 2014 but revived it in 2017 with no objection from Fauci.

Fauci’s NIAID funded the Wuhan Institute of Virology (WIV) in Communist China, where gain-of-function research could be conducted in secret, with no accountability. The WIV also received a shipment of deadly pathogens from a lab in Canada, courtesy of Chinese scientist Dr. Xiangguo Qiu. As Israeli microbiologist Dr. Dany Shoham noted, Dr. Qiu worked closely with four institutions connected to China’s biological weapons development, including the WIV.

In early 2017, Fauci proclaimed there was “no doubt” that president Donald Trump would be confronted with a surprise infectious disease outbreak. In early 2020, Fauci praised China’s handling of the pandemic and in the early going opposed President Trump’s ban on travel from China. Fauci contended that the COVID virus developed naturally in the wild, a view not derived from a replicated scientific study.

Fauci, who commands the NIAID budget of more than $6 billion, did not take kindly to those who found evidence that the COVID virus had been engineered in a lab. Dr. Robert Redfield, director of the Centers for Disease Control, even got death threats for suggesting that the COVID virus leaked from a Chinese lab. New Zealand data scientist Gilles Demaneuf told Vanity Fair he was unsure about the origin but “100 percent sure there was a massive cover-up.”

The late Angelo Codevilla, a former staffer with the Senate intelligence committee, quickly pegged Fauci as a “deep state fraud.” In more than 50 years in government, Dr. Fauci never once had to face the voters. This is the person most responsible for wrecking the booming Trump economy and locking down the workers. The NIAID boss, now 80, showed little if any concern for the suffering Americans were forced to endure. Here is a medical doctor who first causes harm, so it makes sense that such a person would spend taxpayer dollars to torture beagles in Tunisia.

Joe Biden still shows confidence in this Lysenko figure, the highest-paid bureaucrat in the entire federal government. Dr. Fauci now claims that those who criticize him “are actually criticizing science.” Fortunately for embattled Americans, Dr. Fauci recently confirmed his megalomaniac status.

“There comes a time,” Fauci told a McGill University audience, “when you do have to give up what you consider your individual right of making your own decision, for the greater good of society.” 

In reality, what America needs to give up, as soon as possible, is Dr. Fauci himself.

Republicans are calling for Fauci to resign and face prosecution for perjury. As with the dog-torture issue, Democrats should support a full criminal investigation of the NIAID boss.

If a free America is to endure, white coat waste and white coat supremacy will both have to go.

DR. STEVE TURLEY: The Colossal FALL of FAUCI!~Horrifying images have surfaced over the weekend showing cruel animal experiments purportedly funded by Fauci!

★★★ YOUR PATRIOT PATH TO FREEDOM! ★★★

DR. STEVE TURLEY REPORTS:

Dr. Anthony Fauci is under fire as of today like never before! Horrifying images have surfaced over the weekend showing cruel animal experiments purportedly funded by Fauci! In this video, we’re going to look at that controversy, along with NIH officials admitting that US tax dollars were indeed used in gain-of-function research in Wuhan, and stick with me to the very end of this video when we’re going to see why the days for Fauci as the nation’s Covid tsar are indeed coming to an end, you are NOT going to want to miss this!

ALLIE BETH STUCKEY: The REAL Reason Pharma, Fauci & Media Slam Ivermectin~Guest: Dr. Pierre Kory

This episode has been heavily edited to comply with YouTube's policies. You can get the full, uncensored conversation on BlazeTV or Apple Podcasts. Podcast link: https://apple.co/3j2rBQG Today we're talking to Dr. Pierre Kory, president of the Front Line COVID-19 Critical Care Alliance, who has dedicated much of his time to spreading accurate information about COVID and ways to treat the virus. Specifically, Dr. Kory is adamant about correcting the record on ivermectin, which the mainstream media has dubbed nothing more than "horse dewormer." However, the situation is much more nuanced than that, and Dr. Kory explains how the drug works and how it interacts with COVID. We also discuss the deep corruption in the medical industry and the coordinated effort from these major companies to spread disinformation about ivermectin and suppress its use. *Disclaimer: The content of this clip does not provide medical advice. Please seek the advice of local health officials for any COVID-19 and/or COVID vaccine-related questions & concerns.

FDA exposed as a criminal body parts cartel involved in routine harvesting of organs from LIVING human babies

UNIVERSITY OF PITTSBURGH IS A HIVE OF FETAL EXPERIMENTATION-HORRIFYING INFORMATION

Image: FDA exposed as a criminal body parts cartel involved in routine harvesting of organs from LIVING human babies

BY LANCE D. JOHNSON

SEE: https://www.naturalnews.com/2021-10-11-fda-exposed-criminal-body-parts-cartel-organs-from-living-human-babies.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) It will be impossible to take an “FDA approval” seriously, after learning what FDA workers “approve of” behind the scenes.

Using the Freedom of Information Act, Judicial Watch uncovered 198 suspect communication records from the U.S. Food and Drug Administration (FDA). The records unveil a criminal operation within the agency, a ghoulish operation that routinely harvests and traffics organs from LIVING human babies.

The records reveal that the FDA is under contract with a human fetal tissue provider, Advanced Bioscience Resources (ABR). The FDA uses ABR to obtain human heads, organs, and tissue that are strategically harvested from aborted babies. In the records, the FDA even requested “fresh and never frozen” fetal body parts, so they could carry out chimeric research projects involving “humanized mice.”

Organs from 24-week-old abortions are harvested “fresh” and sold to the FDA

Some of the FDA communications were redacted. Judicial Watch was able to uncover these redactions with the help of the court. The redactions included a payment plan for fetal cadaverous procurement. The “service fee” for an intact calvarium taken from babies between 8 to 24 weeks old is $515 per specimen. The FDA’s contract with ABR included an estimated $60,000 in trafficked organs taken strategically from live aborted babies. During a 2016 U.S. Senate Judiciary Committee Investigation, the ABR admitted “that its procurement technicians work inside the abortion facilities, packaging and shipping the aborted baby body parts ‘on the day they are procured.’” Judicial Watch and the court have uncovered several violations of federal law and shone a light on wide-scale crimes against humanity.

“The court also found ‘there is reason to question’ whether the transactions violate federal law barring the sale of fetal organs,” Judicial Watch informs. “Documents previously uncovered in this lawsuit show that the federal government demanded the purchased fetal organs be ‘fresh and never frozen.’”

“Chopping up aborted human beings for their organs and tissue is a moral and legal outrage,” said Judicial Watch President Tom Fitton. “This issue should be front and center in any debate about America’s barbaric abortion industry.”

FDA, NIAID, and the University of Pittsburgh all engaged in criminal fetal organ research

The FDA’s sinister organ harvesting operation coincides with the macabre projects being conducted at the University of Pittsburgh. A separate Judicial Watch lawsuit uncovered 252 pages from the U.S. Department of Health and Human Services. The documents reveal that nearly $3 million in federal funds were handed over to the University of Pittsburgh to create a ‘Tissue Hub’ for human fetal tissue ranging from 6 to 42 weeks gestation.

With a steady flow of taxpayer cash, the university has been collecting live organs and grafting babies’ scalps onto lab rats for research purposes. The research is also funded by grants issued by Dr. Anthony Fauci and the National Institute of Allergy and Infectious Diseases (NIAID). The university has a revolving door with Planned Parenthood, the nation’s largest abortion business. The university has been accused of altering standard abortion procedures to go after organs from babies who are old enough to live outside the womb.

The university’s own researchers were caught discussing the harvesting of kidneys, livers, and hearts from LIVING babies. Nearly 100 members of Congress are calling for transparency from the federal government. The very people who should be launching an investigation into the matter have stayed quiet. University leadership, Allegheny County District Attorney Stephen Zappala, U.S. Attorney Stephen Kaufman, and Attorney General Josh Shapiro have all refused to respond to these serious violations of federal law. Their political reputation and support for abortion are more important than investigating and prosecuting the evil entities behind human experimentation and serious crimes against humanity. Worse yet, these evils are “FDA-approved.”

Sources include:

TheNewAmerican.com

JudicialWatch.org

Judiciary.Senate.gov [PDF]

NaturalNews.com

Brighteon.com

Former Pfizer employee flags FDA study, warns that Pfizer vaccine increases COVID by over 300%

BY LANCE D. JOHNSON

SEE: https://www.naturalnews.com/2021-10-01-former-employee-warns-pfizer-vaccine-increases-covid.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) The fraudulence of covid-19 vaccines is on full display, and the evidence is sitting right out in the open. The full FDA approval for Pfizer’s COMIRNATY vaccine contained clinical proof that inoculation increases COVID infection by over 300 percent!

A former Pfizer employee named Karen Kingston is blowing the whistle on her former employer. Kingston is currently a pharmaceutical marketing expert and biotech analyst. When she scrutinized the full FDA approval for COMIRNATY, she found blatant fraud in Pfizer’s clinical studies.

FDA approves Pfizer’s covid-19 vaccine, even though it increases infection by 300 percent

Kingston brought forth a Briefing Document from the FDA’s advisory committee meeting that took place on September 17, 2021. The title of the document is, “Application for licensure of a booster dose for COMIRNATY (COVID-19 Vaccine, mRNA).” The document includes clinical studies conducted by Pfizer. These studies track the durability of immunity offered by the COMIRNATY vaccine and compare it to immunity observed in unvaccinated people.

“If you get the Pfizer vax, you’re more likely to get COVID” said Kingston, “So, when they weren’t injected, their infection rate was 1.3% and when they got injected, it was 4.34%. It went up by over 300%.” How could the FDA have glossed over this evidence and approved blatant fraud?

Since the vaccine was officially approved, the federal government started applying pressure on businesses across the US, threatening them with extortion and fines if they do not impose vaccine mandates on their employees. The covid-19 vaccines have been injected almost 225 million times into the arms of Americans, causing severe injury and death along the way. Real-world observations also support clinical data showing that the vaccines increase one’s susceptibility to covid-19. In fact, the vaccines increase the viral load in the nostrils of the vaccinated. An August 26 article by Dr. Peter McCullough shows that the covid vaccines allow the vaccinated to carry 251 times the viral load of covid-19 in their nostrils, turning them into the asymptomatic super spreaders they once feared.

Pfizer studies show that being unvaccinated offers greater protection

Medical freedom rights attorney, Thomas Renz, went public with the Pfizer fraud. The Pfizer study involved over 36,000 people. Those who were injected earlier in the study were more likely to come down with covid infections, later on, showing a clear trend of waning immunity. Those put in “high priority” groups, who were vaccinated earlier on, have a 36 percent greater chance of infection, compared to the group that vaccinated later on.

The group that vaccinated, later on, went unvaccinated for 5.1 months longer than the group that got vaccinated early on. This placebo group did not have high rates of infection while they were unvaccinated, even though they went longer without any “protection.” Because of this, Kingston stated that the vaccinated group “have an even higher chance of being infected with COVID-19 than the 36 percent difference indicated by this portion of the study.”

The study even admitted in its conclusion: “An additional analysis appears to indicate that incidence of COVID-19 generally increased in each group of study participants with increasing time post-Dose 2.” Kingston clarified that infection rates “increase over time” when people get two doses of Pfizer mRNA.

Most shocking was the data on the placebo group. In the first four months, the placebo group had “no vaccine protection” and recorded an infection rate of 12.6 cases per 1,000 person-years. The infection rate for the unvaccinated was a meager 1.3 percent.

After their placebo period, the group got “fully vaccinated.” In just a few months, this group became more infectious and showed 43.4 cases per 1,000 person-years. Their infection rate went UP by over 300 percent to a 4.34% infection rate. Mrs. Kingston called this “super alarming.”

“They had less infection when they had no protection. So, that’s a problem,” she said.

Check out Vaccines.News for the latest on the covid-19 vaccine fraud.

Sources include:

LifesiteNews.com

FDA.gov

Papers.SSRN.com

To survive, red states must now NULLIFY the federal government and declare themselves “health freedom zones” that DENOUNCE the FDA, CDC and OSHA

BY MIKE ADAMS

SEE: https://www.naturalnews.com/2021-09-30-red-states-nullify-federal-government-declare-health-freedom-zones.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) With illegitimate occupier-in-chief Joe Biden waging outright war and economic terrorism against red states (see examples below), the leaders of those red states must now nullify federal government overreach in order to prevent their own citizens from being mass murdered by D.C. swamp policies that are intentionally designed to achieve depopulation.

Some of the ways the Biden regime is waging war on red states include:

  • Economic terrorism: Unleashing OSHA to destroy all businesses that won’t enforce vaccine mandates by levying fines of $70,000 per day or even higher.
  • Engineered medicine shortages: Biden recently announced restrictions on shipping monoclonal antibodies to red states in order to maximize covid fatalities in those states.
  • Vaccine mandates: Through vaccine mandates, Biden is committing medical genocide against every American, working to achieve a mass die-off that will leave states in a worsening economic crisis (and humanitarian crisis) as the deaths unfold.
  • Border invasion: The Biden regime and its corrupt DOJ are actively fighting against sensible border security, openly allowing a land invasion of states like Texas and Arizona in order to flood the nation with replacement Democrat voters.
  • Money printing madness: Every dollar printed by the Fed and distributed by the Treasury is actually an instrument of debt that steals purchasing power from the hard-working Americans who produce things. Those producers tend to live in red states, while blue states are the welfare states where more people get handouts that were essentially stolen from the producers in the red states.
  • Election rigging: Biden and other Democrats like Newsom are now institutionalizing never-ending election rigging in order to make sure the will of the people is never honored in any election. Although their own disastrous policies are wildly unpopular, they can continue to maintain power by cheating in elections, just like they cheated in 2020.
  • Outlawing of medicine that works: Notice how the D.C. swamp has attacked ivermectin and made sure no hospital prescribes it to patients? This is also part of the medical genocide agenda, and it’s a war on humanity.
  • Punitive taxation: Under the Biden regime (which is actually run by Obama), the IRS will be handed a mandate to raise taxes on productive American workers, punishing them for having jobs, all while handing out more welfare and entitlements to the illegals who are allowed to invade America by the hundreds of thousands each month.

A long train of abuses: These are all acts of war against red states in particular, and against the American people in general. Any state that follows this “death recipe” will go down with the collapse of America, exactly as long planned by Obiden. (Obama has been working toward the total collapse of the USA since he gained power in 2008. He is now the one running Biden.)

Red states must now denounce and ignore the FDA, CDC, OSHA and other federal agencies that have been weaponized against the people

To survive the planned culling of America’s population, red states must take a stand and publicly denounce the FDA, CDC, OSHA and other weaponized federal agencies (ATF?) that are now overtly working against the interests of the American people.

The FDA serves Big Pharma, not public health or safety. The CDC is a criminal cartel deeply engaged in depopulation crimes against humanity. OSHA is now preparing to commit economic terrorism against America’s small businesses with insane daily fines. The ATF is a gun-running organization (remember Operation Fast & Furious) that seeks to destroy the Second Amendment. You can probably think of other examples yourself…

To survive and thrive, red states must declare themselves to be health freedom sanctuary states that recognize the value of ivermectin, natural medicine, herbal medicine, nutritional medicine and Traditional Chinese Medicine (along with other healing arts). We must purge Big Pharma from its influence peddling and eliminate the pharma stranglehold over public policy before pharma achieves its mass murder agenda.

At the same time, these states must also declare themselves to be First Amendment sanctuary states while blocking YouTube, Facebook, Twitter, Vimeo, Google and other Big Tech tyrants from operating in those states until they agree to abide by First Amendment principles of free speech.

States must prepare their own currencies to get ready for the coming dollar collapse

As part of this nullification effort — Tenth Amendment — states must prepare to roll out their own currencies when the dollar collapses, which now looks to be close at hand. With brain-dead Biden and the Democrats now absurdly claiming that $3.5 trillion in new government spending costs “zero dollars” and adds “zero” to government debt, we have truly reached the blowout phase of the dollar collapse… and the total demise of the dollar isn’t far away. (Soon they will be printing a trillion dollars a week, and then moving toward a trillion a day…)

Any state that isn’t prepared to introduce its own currency when the dollar implodes will find its own citizens and economy literally collapsing into near-instant ruin. Importantly, only a gold-backed currency will be trusted by the citizens in the aftermath of the collapse of the dollar (and the total ruin of every person holding dollar-denominated bank accounts, US stocks, Treasury bills, dollar debt bonds, etc.).

It is now clear that nullification is a matter of survival. We either nullify the treacherous, treasonous federal overreach or we allow Biden to sink us all.

See full detail in today’s Situation Update podcast, which also covers:

  • China’s power grid emergency.
  • Why both China and the corrupt US leadership want World War III.
  • More deaths of pro-vaccine people who mocked anti-vaxxers as stupid morons.
  • OSHA’s economic terrorism against American businesses.
  • The increasing risk of Biden’s handlers invoking the “internet kill switch.”
  • Fuel shortages in the UK, grocery shortages in the USA.
  • The coming “dark winter” of supply line collapse, chaos, violence and vaccine death.

Today’s podcast is longer than usual, nearly 85 minutes. The last 30 minutes are the most powerful:

Brighteon.com/761c37a4-ba9a-438c-8ac8-b33c0a591859

Discover new interviews and podcasts each day at:

https://www.brighteon.com/channels/hrreport

Trick-or-treat? FDA Expected to Approve Pfizer COVID Jab for Children Ages 5 to 11 by Halloween

Trick-or-treat? FDA Expected to Approve Pfizer COVID Jab for Children Ages 5 to 11 by Halloween

BY VERONIKA KYRYLENKO

SEE: https://thenewamerican.com/trick-or-treat-fda-expected-to-approve-pfizer-covid-jab-for-children-ages-5-to-11-by-halloween/;

republished below in full unedited for informational, educational & research purposes:

Former Food and Drug Administration (FDA) Commissioner Dr. Scott Gottlieb, who is also a current Pfizer director, predicted Sunday that the FDA will grant Pfizer’s COVID shot an approval for emergency use in children ages 5 to 11 by the end of October.

In an interview with Face the Nation, Gottlieb said that the Big Pharma company is expecting to have clinical data on its vaccines in young children before the end of September, which will then be filed “within days” with the FDA. He went on to state that the FDA said it then will be a “matter of weeks, not months” to evaluate that data, and then, per his estimates, it would take from four to six weeks for the regulators to green-light the jab for use.

“In a best-case scenario, given that timeline they’ve just laid out, you could potentially have a vaccine available to children aged 5 to 11 by Halloween,” Gottlieb said. He added: “If everything goes well, the Pfizer data package is in order, and the FDA ultimately makes a positive determination, I have confidence in Pfizer in terms of the data that they’ve collected. But this is really up to the Food and Drug Administration to make an objective determination.”

Further, Gottlieb explained that parents, who have “understandable concerns” regarding the use of this vaccine, would have to consult with their child’s pediatrician to determine how to approach the issue of vaccination. Noting that there will be “not a binary approach — do I vaccinate my child or not,” suggesting that he does not view the refusal to inoculate little ones as an option. Gottlieb described some of the details on how a child may be given an upcoming shot: “You could go with one dose for now. You could potentially wait for the lower dose vaccine to be available…. If your child has had COVID, one dose may be sufficient. You could space the doses out more. So there’s a lot of discretion that pediatricians can exercise” depending on the “child’s needs,” per Gottlieb.

Pfizer started testing its jabs on healthy 6-month to 11-year old children just in the end of March, which means that no mid-and long-term side effects of shots could possibly have been studied by now. Also, there is an almost nonexistent chance of young children dying of COVID. Yet, despite these facts, the FDA has seen an enormous amount of pressure from the politicians and a part of the medical community to swiftly approve a COVID shot for children younger than 12.

In the end of August, more than 100 House lawmakers on both sides of the aisle wrote to the FDA asking for an update on its timeline for vaccines for children, citing the current “alarming” situation. 

Around the same time, the American Academy of Pediatrics (AAP), considered the world’s largest and most influential professional association for pediatricians, and also the largest pediatric publisher, sent a letter to the FDA urging the agency to authorize the vaccine for children under 12 “as swiftly as possible.” To those who believe in the authority of expertise and science, it would also be useful to know that the judgment of the seemingly respectable organization might be marred with a financial interest since Pfizer is a major donor — a fact the AAP tried unsuccessfully to hide.  

Last Friday, seemingly responding to the growing pressure, the FDA issued a statement that reflected that they are “eager” to see COVID jabs available for young children and “eager” to get them inoculated “as soon as possible.” Still, while reassuring the public that “the FDA is working around the clock” to get it done, the body did not provide any timeline on when the approval may be issued.

Sure enough, the FDA also stressed that the evaluation of jabs “will not cut any corners.” However, in the same statement, the regulators also said that the safety data on the possible side effects in children would be based on “at least two months” of follow-ups. Now, assuming that “at least two months” does not mean “a lot more than two months,” that certainly does not sound like no “corners” are being cut. Given the already existing concerns in COVID jabs injuring and killing thousands of people, two months of jabs’ safety data in children does not look sufficient enough to recommend it to some 28 million kids.

Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases and President Joe Biden’s top medical advisor, said that getting children vaccinated is an important step toward achieving herd immunity. Dr. Fauci is known as a big proponent of the vaccine mandates, so as soon as the shot gets an OK from the federal regulators, it is expected that he will advocate that the schools require their youngest students to get jabbed. Last week, the Los Angeles Unified School District, the second-largest in the nation, made such a decision for their students older than 12, who are already eligible for the Pfizer shot.  

In May, the FDA expanded the emergency use authorization for the Pfizer-BioNTech vaccine to include individuals from ages 12-15. And on August 23, the FDA granted full approval for Pfizer’s Comirnaty vaccine, which is yet to make it to the American market, for use by people over the age of 16. 

Fitton: Documents show Obama FDA buying fetal heads ‘fresh, never frozen’

Rumble — Judicial Watch President Tom Fitton speaks out on new damning documents showing the Obama-era FDA purchased fetal body parts. One America's John Hines has more from Washington.

FROM: https://rightwinguncut.com/fitton-documents-show-obama-fda-buying-fetal-heads-fresh-never-frozen/: 

Judicial Watch President Tom Fitton speaks out on new damning documents showing the Obama-era FDA purchased fetal body parts. One America’s John Hines has more from Washington.

These people are sick! that explains their demonic push for abortions!;

Why is this not on every major news outlet? We as a country are going to hell in a handbasket;

Because the news is controlled by the Satan worshipers. OAN and Newsmax seem to tell what’s really going on. Of course, the democrats and the fake news will say they’re the ones lying. That’s what Liberals do. They do bad things and blame it on the other side. It’s the first play in their playbook:

HORRORS CONFIRMED: Obama’s FDA purchased “fresh and never frozen” aborted baby heads and other body parts

SEE: https://www.planet-today.com/2021/09/horrors-confirmed-obamas-fda-purchased.html#gsc.tab=0;

republished below in full unedited for informational, educational & research purposes:

(Planet Today) A Freedom of Information Act (FOIA) case filed by the government watchdog group Judicial Watch has revealed that the U.S. Food and Drug Administration (FDA) under Barack Hussein Obama purchased the heads and other body parts of murdered (aborted) unborn human babies in order to conduct “research.”

The FDA claimed that the aborted baby body parts were for a “humanized mice” project that involved experimenting with “human fetal heads, organs, and tissues,” according to 198 pages of now-extracted FDA records.

(Article by Ethan Huff republished from NaturalNews.com)

These “supplies” came from a biotechnology company called Advanced Bioscience Resources (ABR). ABR employee Perrin Lawton reportedly conducted the business deals with the help of FDA officer Kristina Howard, according to unearthed documents.

A lawsuit filed by Judicial Watch sought the records for “all contracts and related documentation on disbursement of funds, procedural documents and communications between FDA and ABR for the provision of human fetal tissue to be used in humanized mice research.”

A federal court responded by ordering that the government provide even more details about the purchase of these human body parts, “including ‘line item prices,’ or the price per organ the government paid to ABR,” Judicial Watch announced about the ongoing case.

“The court also found ‘there is reason to question’ whether the transactions violate federal law barring the sale of fetal organs. Documents previously uncovered in this lawsuit show that the federal government demanded the purchased fetal organs be ‘fresh and never frozen,'” Judicial Watch added in a statement.

Baby murder is big money in America

In 2012, right after Obama had been reelected for his second term, an agreement was made between the FDA and ABR to transact “$12,000 worth of ’tissue procurement for humanized mice.'” That transaction ended up costing some $60,000 when all was said and done.

In some cases, aborted baby body parts came at a rate of $230 per “tissue,” with two per box plus shipping. The delivery of “fetal livers and thymuses,” meanwhile, cost a bit more at $580 a “set,” with some of the more “premium” organs costing $685 a pop.

To obtain an “intact calvarium,” which is just a fancy word for an uncrushed baby’s skull, the FDA was billed $515 each by ABR.

“The HM [humanized mice] are created by surgical implantations of human tissue into mice that have multiple genetic mutations that block the development of the mouse immune system at a very early stage,” a government researcher reportedly told ABR at the time.

“The absence of the mouse immune system allows the human tissues to grow and develop into functional human tissues … In order for the humanization to proceed correctly we need to obtain fetal tissue with a specific set of specialized characteristics.”

Obtusely, Obama actually had the gall to get up in front of the world and condemn this type of medical experimentation with aborted baby body parts – in Africa, anyway.

You read that right: Obama expressed opposition to the chopping up of human babies for the purpose of doing “Frankenstein” experiments on them, but only in Africa. Here in the United States, he oversaw this very same wickedness, which was funded with American taxpayer dollars.

“Chopping up aborted human beings for their organs and tissue is a moral and legal outrage,” says Judicial Watch President Tom Fitton. “This issue should be front and center in any debate about America’s barbaric abortion industry.”

Last year, Judicial Watch reported on how the National Institute of Health (NIH), where Tony Fauci works, has been doing much the same thing via the University of Pittsburgh, which has since been outed as one of the major “tissue hubs” where aborted baby body parts are processed and sold for profit.

The latest news about the abortion racket can be found at Abortions.news.

 

Fauci bioweapons funding CONFIRMED, smoking gun proves covid vaccines based on govt biowarfare program

BY MIKE ADAMS

SEE: https://www.naturalnews.com/2021-09-08-fauci-bioweapons-funding-confirmed-smoking-gun-proves-covid-vaccines-biowarfare.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) Thanks to a FOIA request by The Intercept, we now have smoking-gun proof that Anthony Fauci directed NIH funding for bioweapons research on SARS-CoV-2 (via “gain-of-function” experiments) under the cover of the Chinese Communist Party. The 900+ pages of once-secret documents also confirm that the United States government originated the bioweapons research and funded it to completion. After Trump banned biological weapons programs in the United States, Fauci and others conspired to criminally conduct illegal research by shifting the technology to China (and laundering US taxpayer money through the EcoHealth Alliance to fund it).

As detailed by The Intercept:

NEWLY RELEASED DOCUMENTS provide details of U.S.-funded research on several types of coronaviruses at the Wuhan Institute of Virology in China. The Intercept has obtained more than 900 pages of documents detailing the work of EcoHealth Alliance, a U.S.-based health organization that used federal money to fund bat coronavirus research at the Chinese laboratory.

One of the grants, titled “Understanding the Risk of Bat Coronavirus Emergence,” outlines an ambitious effort led by EcoHealth Alliance President Peter Daszak to screen thousands of bat samples for novel coronaviruses. The research also involved screening people who work with live animals.

The bat coronavirus grant provided EcoHealth Alliance with a total of $3.1 million, including $599,000 that the Wuhan Institute of Virology used in part to identify and alter bat coronaviruses likely to infect humans.

Fauci lied, millions died

In essence, thanks to the FOIA revelations, we now know that:

  1. Fauci lied under oath when he claimed he never funded gain-of-function research. (Where is the FBI raid on Fauci?)
  2. The entire COVID “pandemic” was built as a biological weapons program from the very start.
  3. Fauci and others committed not merely criminal acts in violation of biological weapons research bans, he also committed treason against the United States of America by handing weapons of mass destruction to America’s communist enemy (China) when then deployed the weapon system against America.

We also therefore know that the vaccine is an extension of the bioweapons program funded by Fauci, since the spike protein incorporated into covid vaccines was developed through Fauci-funded gain-of-function research.

With this knowledge now being made public thanks to The Intercept, all vaccines should be halted worldwide, and criminal indictments should be leveled against Fauci and the thousands of co-conspirators who were complicit in this operation, which includes Big Pharma CEOs, virology scientists, and freedom-hating politicians who used all this as an excuse to push toxic bioweapons onto the population via “vaccine” mandates.

BOMBSHELL: The US government started this as a MERS bioweapons program to mass murder people in the Middle East, but it was switched to murdering Americans when Trump took power

The other huge bombshell now emerging from all this is that it appears the US government was originally planning to deploy its bioweapons as a MERS (Middle Eastern Respiratory Syndrome) virus to mass murder political enemies in Iran (and other nations) under “President Clinton” (who was slated to take office in 2017 after the 2016 election was rigged). But when Trump’s military intelligence white hats blocked the election rigging of 2016 and Trump took office, the bioweapons program was redirected to focus on killing Americans and dethroning Trump with the coordinated covid-rigged election scheme of 2020.

So the bioweapons that the US government originally planned to dump on the people of the Middle East ended up being refocused on SARS-CoV and placed into vaccines to be injected into US soldiers and 200+ million American citizens, all in an effort to carry out mass genocide against the American people and its active duty defenders. All along, Fauci was taking orders from the Obama / Clinton cartel which had sought a seamless transition of power to the Clinton regime but was thwarted by the outpouring of popular support for Trump.

Thus, by definition, Fauci, Obama, Biden, and the U.S. deep state have been working with communist China to build and deploy weapons of mass destruction against the American people. Nearly all Democrats are fully on board with this effort, since they hate America and openly call for the killing of conservatives. Shockingly, they’re also all-in on committing vaccine suicide by injecting themselves with the very bioweapon that was deployed to stop Trump. So what we’re about to witness in the years ahead is the mass death of Democrats and whatever conservatives have been propagandized enough to inject themselves with the death shots labeled “vaccines.”

Vaccines are just the first step in a binary weapon system that has yet to be fully deployed

Finally, the vaccines are not designed to kill people immediately upon being injected. They’re actually designed to impair the immune system and prime the body to overreact to a future release of a viral variant that sends the body into immune reaction overdrive. This is called Antibody-Dependent Enhancement, and for it to be fully invoked, a new variant must be introduced and circulated that evades the antibodies produced by the current vaccines (what we call covid vax 1.0). It appears that the Delta variant has already achieved somewhere around a 65% evasion, but upcoming variants will demonstrate even stronger evasion/escape properties.

The real bombshell is that the same Fauci / Daszak / Baric bioweapons program that built SARS-CoV-2 could have already constructed a radical variant that functions as the second part in the binary weapon system. This new variant — perhaps one that’s already released or soon to be released into the wild — would result in mass fatalities of those who took covid vaccines, even if they survived the more immediate vaccine adverse reactions such as blood clotting and heart attacks.

Get the full, shocking details in today’s bombshell Situation Update podcast:

Brighteon.com/37495bd5-40d4-4f32-b452-63685b2b9321

Find more breaking news interviews and videos each day at:

https://www.brighteon.com/channels/hrreport

 

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