Judicial Watch and New York City Settle Federal Lawsuit on Voter Registration Clean-Up after City Removes 441,083 Ineligible Names from Voter Rolls

DECEMBER 28, 2022|JUDICIAL WATCH

Washington, DC – Judicial Watch announced today that it is settling a federal election integrity lawsuit against New York City after the city removed 441,083 ineligible names from the voter rolls and promised to take reasonable steps going forward to clean its voter registration lists

Judicial Watch filed a lawsuit in July against New York City after it failed to clean voter rolls for years. The lawsuit, filed under the National Voter Registration Act (NVRA), pointed out that New York City removed only 22 names under the federal law over six years (Judicial Watch v Valentine et al. (No.1:22-cv-03952)).

The Judicial Watch lawsuit detailed that New York City’s “own recent data concedes that there were only 22 total” removals under this provision “during a six-year period, in a city of over 5.5 million voters. These are ludicrously small numbers of removals given the sizable populations of these counties.” Moreover, the “almost complete failure of Kings, Queens, New York, Bronx, and Richmond Counties, over a period of at least six years, to remove voters” under a key provision of federal law “means that there are untold numbers of New York City registrations for voters who are ineligible to vote at their listed address because they have changed residence or are otherwise ineligible to vote.”

Today’s announced settlement details how the city responded to Judicial Watch’s notice about its voting roll deficiencies with a massive clean-up:

[The Board of Elections] notified Judicial Watch that, in February 2022, they removed, pursuant to Section 8(d)(1)(B) of the NVRA, 82,802 registrations in Bronx County, 128,093 in Kings County, 145,891 in New York County, 66,010 in Queens County, and 18,287 in Richmond County, for a total of 441,083 registrations.

[The Board of Elections] notified Judicial Watch that going forward they intend to cancel registrations pursuant to Section 8(d)(1)(B) in each odd-numbered year in the months following a federal election.

Specifically, the city also agrees to track in detail report its voter roll maintenance efforts through 2025:

For both 2023 and 2025the [Board of Elections] will notify Judicial Watch … on or before March 31, by means of separate excel spreadsheets for Bronx County, Kings County, New York County, Queens County, and Richmond County, of the number of removals, including removals pursuant to … the NVRA, made during the previous two years.

The NVRA requires states to “conduct a general program that makes a reasonable effort to remove” from the rolls the names of ineligible voters” who have died or changed residence. Among other things, the law requires registrations to be cancelled when voters fail to respond to address confirmation notices and then fail to vote in the next two general federal elections. In 2018, the Supreme Court confirmed that such removals are mandatory (Husted v. A. Philip Randolph Inst. (138 S. Ct. 1833, 1841-42 (2018)).

This historic settlement is a major victory for New York voters who will benefit from cleaner voter rolls and more honest elections. Judicial Watch is pleased that New York City officials quickly moved to remove 441,000 outdated registrations from the rolls. We look forward to working together under this federal lawsuit settlement to ensure New York City maintains cleaner rolls for future elections,” stated Judicial Watch President Tom Fitton.

Judicial Watch is a national leader in voting integrity and voting rights. As part of its work, Judicial Watch assembled a team of highly experienced voting rights attorneys who stopped discriminatory elections in Hawaii, and cleaned up voter rolls in California, Ohio, Indiana, and Kentucky, among other achievements.

Kentucky also began a cleanup of hundreds of thousands of old registrations last year after it entered into a consent decree to end another Judicial Watch lawsuit.

In February 2022, Judicial Watch settled a voter roll clean-up lawsuit against North Carolina and two of its counties after the North Carolina removed over 430,000 ineligible names from the voter rolls.

In March 2022, a Maryland court ruled in favor of Judicial Watch’s challenge to Maryland’s Democratic legislature “extreme” congressional redistricting gerrymander.

In May 2022, Judicial Watch sued Illinois on behalf of Congressman Mike Bost and two other registered Illinois voters to prevent state election officials from extending Election Day for 14 days beyond the date established by federal law.

Robert Popper, Judicial Watch senior attorney, leads its election law program. Popper was previously in the Voting Section of the Civil Rights Division of the Justice Department, where he managed voting rights investigations, litigations, consent decrees, and settlements in dozens of states.

Ethan Leonard, Esq. and Neal Brickman, Esq. of The Law Offices of Neal Brickman, P.C. in New York City assisted Judicial Watch in the lawsuit.

Source: https://www.judicialwatch.org/jw-and-nyc-settle-lawsuit/

What Do the Records Reveal About Covid-19 Vaccine and Boosters?

Here’s just a few that have been uncovered

Rest assured, this is just the tip of the iceberg……there’s more

FOIA Judicial Watch has uncovered a substantial amount of information regarding COVID-19 issues:

  • In October 2020, Judicial Watch received FDA records that detailed pressure for COVID-19 vaccine booster approval and use.
  • NIH records revealed an FBI “inquiry” into the NIH’s controversial bat coronavirus grant tied to the Wuhan Institute of Virology. The records also show National Institute of Allergy and Infectious Diseases (NIAID) officials were concerned about “gain-of-function” research in China’s Wuhan Institute of Virology in 2016. The Fauci agency was also concerned about EcoHealth Alliance’s lack of compliance with reporting rules and use of gain-of-function research in the NIH-funded research involving bat coronaviruses in Wuhan, China.
  • HHS records revealed that from 2014 to 2019, $826,277 was given to the Wuhan Institute of Virology for bat coronavirus research by the NIAID.
  • NIAID records showed that it gave nine China-related grants to EcoHealth Alliance to research coronavirus emergence in bats and was the NIH’s top issuer of grants to the Wuhan lab itself. The records also included an email from the vice director of the Wuhan Lab asking an NIH official for help finding disinfectants for decontamination of airtight suits and indoor surfaces.
  • HHS records included an “urgent for Dr. Fauci ” email chain, citing ties between the Wuhan lab and the taxpayer-funded EcoHealth Alliance. The government emails also reported that the foundation of U.S. billionaire Bill Gates worked closely with the Chinese government to pave the way for Chinese-produced medications to be sold outside China and help “raise China’s voice of governance by placing representatives from China on important international counsels as high level commitment from China.”
  • HHS records included a grant application for research involving the coronavirus that appears to describe “gain-of-function” research involving RNA extractions from bats, experiments on viruses, attempts to develop a chimeric virus and efforts to genetically manipulate the full-length bat SARSr-CoV WIV1 strain molecular clone.
  • HHS records showed the State Department and NIAID knew immediately in January 2020 that China was withholding COVID data, which was hindering risk assessment and response by public health officials.
  • University of Texas Medical Branch (UTMB) records show the former director of the Galveston National Laboratory at the University of Texas Medical Branch (UTMB), Dr. James W. Le Duc warned Chinese researchers at the Wuhan Institute of Virology of potential investigations into the COVID issue by Congress.
  • HHS records regarding biodistribution studies and related data for the COVID-19 vaccines show a key component of the vaccines developed by Pfizer/BioNTech, lipid nanoparticles (LNPs), were found outside the injection site, mainly the liver, adrenal glands, spleen and ovaries of test animals, eight to 48 hours after injection.
  • Records from the Federal Select Agent Program (FSAP) reveal safety lapses and violations at U.S. biosafety laboratories that conduct research on dangerous agents and toxins.
  • HHS records include emails between National Institutes of Health (NIH) then-Director Francis Collins and Anthony Fauci, the director of National Institute of Allergy and Infectious Diseases (NIAID), about hydroxychloroquine and COVID-19.
  • HHS records show that NIH officials tailored confidentiality forms to China’s terms and that the World Health Organization (WHO) conducted an unreleased, “strictly confidential” COVID-19 epidemiological analysis in January 2020.
  • Fauci emails include his approval of a press release supportive of China’s response to the 2019 novel coronavirus.

A “Pharmacokinetics Written Summary” marked “Confidential,” indicates that the information it contains is related to the mRNA-1273 (Moderna vaccine) strain, however, much of the data comes from work with mRNA-1647. The study states:

The results of a biodistribution study of mRNA-1647 support the development of mRNA-1273.

***

The biodistribution of mRNA-1647 was evaluated in a non-Good Laboratory Practice (GLP), single-dose, intramuscular (IM) injection study in Sprague Dawley rats…. mRNAs that are within an LNP of the same composition (e.g., mRNA-1273 and mRNA-1647) are expected to distribute similarly.

  • No absorption studies with mRNA-1273 [used in Moderna’s COVID vaccine] have been performed.
  • No metabolism studies with mRNA-1273 have been performed.
  • No excretion studies with mRNA-1273 have been performed.
  • No PK [pharmacokinetic] studies with mRNA-1273 have been performed.
  • No other PK studies with mRNA-1273 have been performed.

The “Summary” indicates:

According to PubMed.gov, “Pharmacokinetics studies are performed to clarify the absorption, distribution, metabolism, and excretion of drug candidates…[and] are required for establishing the efficacy and safety in humans.”)

A separate study submitted to the FDA sponsored by Moderna Therapeutics Inc. and conducted by Charles River Laboratories in Montreal, Canada is titled “A Single Dose Intramuscular Injection Tissue Distribution Study of mRNA-1647 in Male Sprague-Dawley Rats” in which “[t]he objective … was to determine the tissue distribution of mRNA-1647,” as opposed to mRNA-1273 used in Moderna’s COVID vaccine.

In one appendix to the study, a “clarification” was issued in the toxicokinetic report regarding the half-life of mRNA injected into the rats, noting:The average value of terminal half-life for the muscle (i.e. injection site) in Sections 4.2 and 5 of the toxicokinetic report should be read 14.9 [hours] instead of 8.39 [hours] based on the results of the toxicokinetic evaluation.”

The study further notes that the wording of the conclusion was modified to read, “The half-life … of mRNA-1647 was reliably estimated in muscle (site of injection), proximal popliteal and axillary distal lymph nodes, and spleen with average values for all construct t½ [half-life] of 14.9 8.39, 34.8, 31.1 and 63.0 hours, respectively.” [Emphasis in original]

Another appendix, titled “Summary Mean (±SE) mRNA-1647 Pharmacokinetic Parameters in Sprague-Dawley Rat in Plasma and Tissues Following 100μg Intramuscular Injection Administration of mRNA-1647 on Day 1,” reveals that, in addition to distributing to the muscle site, lymph nodes and spleen, the mRNA particles also distributed to the bone marrow, brain, eyes, heart, liver, lungs, stomach and testes.

A separate study indicates that the mRNA-1647 particles injected into rats were “observed in muscle (i.e. site of injection), followed by proximal (popliteal) lymph nodes, axillary lymph nodes and spleen, suggesting the mRNA-1647 distribution to the circulation by lymph flow.” (The mRNA was delivered via “lipid nanoparticle dispersion.”)

“These previously hidden records about the COVID-19 vaccine safety and efficacy studies raise a number of disturbing questions,” said Judicial Watch President Tom Fitton. “The fact that it has taken a federal lawsuit to get access to this material is yet another scandal.”

Sources :

FAUCI EMAILS

THAT LITTLE BLACK BOOK… The Clinton/Epstein Connection

According to records obtained by the Daily Mail, between 1993 and 1995, Jeffrey Epstein visited President Bill Clinton’s White House 17 times, bringing with him a total of eight women.

The convicted sex offender had connections to many celebrities, journalists and prominent political figures, including Clinton. Many of them were listed in Epstein’s little black book.

In its report on Epstein’s many visits to the Clinton White House, the Daily Mail noted that hanging on the walls of Epstein’s mansion in Palm Beach, Florida, were photos of these visits and a few of the women he had with him.

In addition to Epstein’s longtime partner, Ghislaine Maxwell, the names of the other seven women who accompanied him to the Clinton White House were listed in the report.

Maxwell was recently convicted of several crimes related to her complicity in the sex-trafficking crimes of Epstein.

The Daily Mail said three of the women named were Epstein’s former girlfriends — Celina Midelfart, Eva Andersson-Dubin and Francis Jardine.

The other women in the photos were Jennifer Garrison, Shelley Gafni, Jennifer Driver and Lyoubov Orlova.

As this news surrounding Bill Clinton continues to develop, one can just imagine Hillary tensing up with frustration and thinking to herself, “Not again!”

After all, her husband has been accused of sexually assaulting and harassing several women over the years, and he was impeached for lying about his sexual relationship with a White House intern.

It’s unclear how many additional prominent figures were involved in Epstein’s crimes.

Britain’s Prince Andrew faces a lawsuit over allegations that he sexually assaulted one of Epstein’s victims when she was 17 years old.

Andrew has denied any wrongdoing, but Queen Elizabeth II chose to strip him of his royal titles on Thursday.

Will other prominent political figures — former U.S. presidents, for example — face similar legal proceedings related to their relationships with Jeffrey Epstein?

Only time will tell.

Continue reading “THAT LITTLE BLACK BOOK… The Clinton/Epstein Connection”

Judicial Watch Files Civil Rights Lawsuit for Daily Caller News Foundation and Reporter against Chicago Mayor Lori Lightfoot for Racial Discrimination

Judicial Watch Files Civil Rights Lawsuit for Daily Caller News Foundation and Reporter against Chicago Mayor Lori Lightfoot for Racial Discrimination

(Washington, DC) Judicial Watch today filed a lawsuit on behalf of the Daily Caller News Foundation and reporter Thomas Catenacci against Chicago Mayor Lori Lightfoot for violating their First Amendment Rights and Catenacci’s right to equal protection under the Fourteenth Amendment (Catenacci et al v. Lightfoot (No. 1:21-cv-02852)).

The lawsuit was filed in the United States District Court for the Northern District of Illinois, Eastern Division.

On May 18, 2021, Mayor Lightfoot’s office informed multiple reporters that she would grant one-on-one interviews, “only to Black or Brown journalists.” The next day, the mayor released a letter doubling down on her discriminatory policy. Since that time, the Mayor has granted at least one interview request from a self-identified Latino reporter and none to white reporters.

Judicial Watch filed the lawsuit after Catenacci, a white male, emailed Mayor Lightfoot’s office requesting a one-on-one interview with the Mayor. The office never replied to the request or to two additional follow up emails from Catenacci.

The lawsuit alleges Mayor Lightfoot purposefully discriminated against Catenacci, “because of his race by stating that she would only grant interview requests from ‘journalists of color’….”

“Preventing journalists from doing our jobs in such a blatantly discriminatory way is wrong and does a disservice to our readers who come from all backgrounds,” said Daily Caller reporter Thomas Catenacci. “Every journalist and every person who consumes the news should be concerned by Mayor Lightfoot’s actions. This affects everyone. I look forward to holding the mayor accountable.”

“It’s absurd that an elected official believes she discriminate on the basis of race. Mayor Lightfoot’s decision is clearly blocking press freedom through racial discrimination,” Daily Caller News Foundation Editor-in-Chief Ethan Barton said.

“Racial discrimination has no place in America, especially in the halls of government,” said Judicial Watch President Tom Fitton. “Mayor Lightfoot’s admitted policy of race-based discrimination is flagrantly illegal and immoral. Simply put, we’re asking the court to find Mayor Lightfoot’s racist abuse unlawful.”

Christine Svenson of Svenson Law Offices in Chicago, Illinois, is assisting Judicial Watch with the lawsuit.

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“Circling-Back” to 11.26.2020. Phill Kline, former Kansas Attorney General & current Director of the Amistad

11.26.2020

BREAKING:

Phill Kline, former Kansas Attorney General & current Director of the Amistad

Project: “We already have suits in 6 states, but we’re filing more based on this new data.

A series of decisions at the local level, funded & encouraged by the flow of $350M of #MarkZuckerburg monies that allowed for the infusion of these questionable or fraudulent ballots into the stream to be counted. The analysis, using gov’t data and then calling out to voters, asking them about their behavior and getting them to SIGNED affidavits, is that in EACH ONE of these swings states, there are 100’s of THOUSANDS of ballots in question.

In addition to the ballots in WI [up to 150k improperly filed/counted] we’ve identified over 12,000 REPUBLICANS who voted, whose votes WERE NOT COUNTED according to the state’s data. So what you had was:

• $350M coming in

• the creation of all this drop-box

• consolidated counting centers in the urban core around the nation

• #MarkZuckerburg money paying the election judges & officials inside the rooms…

• while the Republicans in America were kicked out of the counting room.

That CANNOT & SHOULD NOT STAND AS A FAIR and INTEGRAL ELECTION…

#MarkZuckerburg’s monies alone matched the federal gov’t appropriations for elections this year. $400M.

#Google:also gave money to this effort.

• We now have evidence pursuant to court order … that they actually told local election officials how to manage the election in these core Democrat areas where you see all the problems.

That was #MarkZuckerburg and a group called “The Center for Tech & Civic Life”.

I give you this thought:

They told America we need to consolidate counting centers, for COVID! We’re going to create a crowd, to protect us … from COVID!

That makes no sense. The reason they did it, is because they didn’t want Republicans to see, and they wanted to infuse fraudulent ballots … and they did it!

Suit filed in GA at the time of this note. There where 200k ballots.

Another link: https://mb.ntd.com/phill-kline-new-amistad-project-election-lawsuit-500-million-to-increase-votes-in-democratic-strongholds_545391.html

W.H.O and World Leaders have serious questions to answer in the upcoming trials for ‘Crimes against Humanity’

W.H.O and World Leaders have serious questions to answer in the upcoming trials for ‘Crimes against Humanity’

THE DAILY EXPOSE • MAY 10, 2021

Nuremberg Trial 2.0 is in preparation, with a class action lawsuit supported by thousands of lawyers and medical professionals worldwide, led by the American-German lawyer Reiner Fuellmich, who is prosecuting those responsible for the Covid-19 scandal manipulated by the Davos Forum.

In this respect, it is worth recalling that Reiner Fuellmich is the lawyer who succeeded in condemning the automobile giant Volkswagen in the case of the tampered catalytic converters, as well as succeeding in condemning Deutsche Bank as a criminal enterprise.

According to Reiner Fuellmich, all the frauds committed by German companies are derisory compared to the damage that the Covid-19 crisis has caused and continues to cause. This Covid-19 crisis should be renamed the “Covid-19 Scandal” and all those responsible should be prosecuted for civil damages due to manipulations and falsified test protocols. Therefore, an international network of business lawyers will plead the biggest tort case of all time, the Covid-19 fraud scandal, which has turned into the largest crime against humanity to ever be committed.

A Covid-19 commission of inquiry was set up in July 2020 on the initiative of a group of German lawyers with the aim of bringing an international class action lawsuit using Anglo-Saxon law.

Here’s what Reiner Fuellmich had to say on the findings of the inquiry and the questions to be answered in the forthcoming trial against the WHO and World Leaders for crimes against humanity –

The hearings of around 100 internationally renowned scientists, doctors, economists and lawyers, which have been conducted by the Berlin Commission of Inquiry into the Covid-19 affair since 10.07.2020, have in the meantime shown with a probability close to certainty that the Covid- 19 scandal was at no time a health issue.

Rather, it was about solidifying the illegitimate power (illegitimate because it was obtained by criminal methods) of the corrupt “Davos clique” by transferring the wealth of the people to the members of the Davos clique, destroying, among other things, small and medium-sized enterprises in particular. Platforms such as Amazon, Google, Uber, etc. could thus appropriate their market share and wealth.

The three major questions to be answered in the context of a judicial approach to the Corona Scandal are:

1) Is there a corona pandemic or is there only a PCR-test pandemic? Specifically, does a positive PCR-test result mean that the person tested is infected with Covid-19, or does it mean absolutely nothing in connection with the Covid-19 infection?

2) Do the so-called anti-corona measures, such as the lockdown, mandatory face masks, social distancing, and quarantine regulations, serve to protect the world’s population from corona? Or do these measures serve only to make people panic so that they believe, without asking any questions, that their lives are in danger — so that, in the end, the pharmaceutical and tech industries can generate huge profits from the sale of PCR tests, antigen and antibody tests and vaccines, as well as the harvesting of our genetic fingerprints?

3) Is it true that the German government was massively lobbied, more so than any other country, by the chief protagonists of this so-called corona pandemic (Mr. Drosten, virologist at Charité Hospital in Berlin; Mr. Wieler, veterinarian and head of the German equivalent of the CDC, the RKI; and Mr. Tedros, head of the World Health Organization or WHO) because Germany is known as a particularly disciplined country and was therefore to become a role model for the rest of the world for its strict and, of course, successful adherence to the corona measures?

Answers to these three questions are urgently needed because the allegedly new and highly dangerous coronavirus has not caused any excess mortality anywhere in the world, and certainly not here in Germany.

But the anti-corona measures, whose only basis are the PCR-test results, which are in turn all based on the German Drosten test, have, in the meantime, caused the loss of innumerable human lives and have destroyed the economic existence of countless companies and individuals worldwide.

These were the conclusions of the committee –

‘The corona crisis must be renamed the “Corona Scandal”

It is:

• The biggest tort case ever
• The greatest crime against humanity ever committed

Those responsible must be:

• Criminally prosecuted for crimes against humanity
• Sued for civil damages

Deaths:

• There is no excess mortality in any country
• Corona virus mortality equals seasonal flu
• 94% of deaths in Bergamo were caused by transferring sick patients to nursing homes where they infected old people with weak immune systems
• Doctors and hospitals worldwide were paid to declare deceased victims of Covid-19
• US states with and without lockdowns have comparable disease and mortality statistics

Autopsies showed:

• Fatalities almost all caused by serious pre-existing conditions
• Almost all deaths were very old people
• Sweden (no lockdown) and Britain (strict lockdown) have comparable disease and mortality statistics

Health:

• Hospitals remain empty and some face bankruptcy
• Populations have T-cell immunity from previous influenza waves
• Herd immunity needs only 15-25% population infection and is already achieved
• Only when a person has symptoms can an infection be contagious

Tests:

• Many scientists call this a PCR-test pandemic, not a corona pandemic
• Very healthy and non-infectious people may test positive
• Likelihood of false-positives is 89-94% or near certainty
• Prof. Drosten developed his PCR test from an old SARS virus without ever having seen the real Wuhan virus from China
• The PCR test is not based on scientific facts with respect to infections
• PCR tests are useless for the detection of infections
• A positive PCR test does not mean an infection is present or that an intact virus has been found
• Amplification of samples over 35 cycles is unreliable but WHO recommended 45 cycles

Illegality:

• The German government locked down, imposed social-distancing/ mask-wearing on the basis of a single opinion
• The lockdown was imposed when the virus was already retreating
• The lockdowns were based on non-existent infections
• Former president of the German federal constitutional court doubted the constitutionality of the corona measures
• Former UK supreme court judge Lord Sumption concluded there was no factual basis for panic and no legal basis for corona measures
• German RKI (CDC equivalent) recommended no autopsies be performed
• Corona measures have no sufficient factual or legal basis, are unconstitutional and must be repealed immediately
• No serious scientist gives any validity to the infamous Neil Ferguson’s false computer models warning of millions of deaths
• Mainstream media completely failed to report the true facts of the so-called pandemic
• Democracy is in danger of being replaced by fascist totalitarian models
• Drosten (of PCR test), Tedros of WHO, and others have committed crimes against humanity as defined in the International Criminal Code
• Politicians can avoid going down with the charlatans and criminals by starting the long overdue public scientific discussion

Conspiracy:

• Politicians and mainstream media deliberately drove populations to panic
• Children were calculatedly made to feel responsible “for the painful tortured death of their parents and grandparents if they do not follow Corona rules”
• The hopeless PCR test is used to create fear and not to diagnose
• There can be no talk of a second wave

Injury and damage:

• Evidence of gigantic health and economic damage to populations

Anti-corona measures have:

• Killed innumerable people
• Destroyed countless companies and individuals worldwide
• Children are being taken away from their parents
• Children are traumatized en masse
• Bankruptcies are expected in small- and medium-sized businesses

Redress:

• A class action lawsuit must be filed in the USA or Canada, with all affected parties worldwide having the opportunity to join
• Companies and self-employed people must be compensated for damages’

Is the writing on the wall for Gates, Hancock, Fauci and friends? Well the lawsuits have been filed and Reiner Fuellmich’s track record certainly suggests they don’t stand a chance.

COVID Fraud – Legal proceedings begin against W.H.O and World Leaders for ‘Crimes against Humanity’

COVID Fraud – Legal proceedings begin against W.H.O and World Leaders for ‘Crimes against Humanity’

THE DAILY EXPOSE • MAY 7, 2021

A team of over 1,000 lawyers and over 10,000 medical experts led by Dr. Reiner Fuellmich have begun legal proceedings against the CDC, WHO & the Davos Group for crimes against humanity.

Fuellmich and his team present the faulty PCR test and the order for doctors to label any comorbidity death as a Covid death as fraud. The PCR test was never designed to detect pathogens and is 100% faulty at 35 cycles. All the PCR tests overseen by the CDC are set at 37 to 45 cycles. The CDC admits that any tests over 28 cycles are not admissible for a positive reliable result. This alone invalidates over 90% of the alleged covid cases / ”infections” tracked by the use of this faulty test.

In addition to the flawed tests and fraudulent death certificates, the “experimental” vaccine itself is in violation of Article 32 of the Geneva Convention. Under Article 32 of the 1949 Geneva Convention IV, “mutilation and medical or scientific experiments not necessitated by the medical treatment of a protected person” are prohibited. According to Article 147, conducting biological experiments on protected persons is a grave breach of the Convention.

The “experimental” vaccine is in violation of all 10 of the Nuremberg Codes which carry the death penalty for those who seek to violate these International Laws.

The “vaccine” fails to meet the following five requirements to be considered a vaccine and is by definition a medical “experiment” and trial:

Provides immunity to the virus
This is a “leaky” gene therapy that does not provide immunity to Covid and claims to reduce symptoms yet double-vaccinated are now 60% of the patients requiring ER or ICU with covid infections.

Protects recipients from getting the virus
This gene-therapy does not provide immunity and double-vaccinated can still catch and spread the virus.

Reduces deaths from the virus infection
This gene-therapy does not reduce deaths from the infection. Double-Vaccinated infected with Covid have also died.

Reduces circulation of the virus
This gene-therapy still permits the spread of the virus as it offers zero immunity to the virus.

Reduces transmission of the virus
This gene-therapy still permits the transmission of the virus as it offers zero immunity to the virus.

The following violations of the Nuremberg Code are as follows:

Nuremberg Code #1: Voluntary Consent is Essential

No person should be forced to take a medical experiment without informed consent. Many media, political and non-medical persons are telling people to take the shot. They offer no information as to the adverse effects or dangers of this gene-therapy. All you hear from them is – “ safe and effective” and “ benefits outweigh the risks.” Countries are using lockdowns, duress and threats to force people to take this vaccine or be prohibited to participate in free society under the mandate of a Vaccine Passport or Green Pass. During the Nuremberg trials, even the media was prosecuted and members were put to death for lying to the public, along with many of the doctors and Nazis found guilty of Crimes Against Humanity.

Nuremberg Code #2: Yield Fruitful Results Unprocurable By Other Means

As listed above, the gene-therapy does not meet the criteria of a vaccine and does not offer immunity to the virus. There are other medical treatments that yield fruitful results against Covid such as Ivermectin, Vitamin D, Vitamin C, Zinc and boosted immune systems for flu and colds.

Nuremberg Code #3: Base Experiments on Results of Animal Experimentation and Natural History of Disease

This gene therapy skipped animal testing and went straight to human trials. In mRNA research that Pfizer used – a candidate study on mRNA with rhesus macaques monkeys using BNT162b2 mRNA and in that study all the monkeys developed pulmonary inflammation but the researchers considered the risk low as these were young healthy monkeys from the age of 2-4. Israel has used Pfizer and the International Court of Law has accepted a claim for 80% of the recipients having pulmonary inflammation from being injected with this gene-therapy. Despite this alarming development Pfizer proceeded to develop their mRNA for Covid without animal testing.

Nuremberg Code #4: Avoid All Unnecessary Suffering and Injury

Since the rollout of the experiment and listed under the CDC VAERS reporting system over 4,000 deaths and 50,000 vaccine injuries have been reported in America. In the EU over 7,000 deaths and 365,000 vaccine injuries have been reported. This is a grievous violation of this code.

Nuremberg Code #5: No Experiment to be Conducted if There’s Reason to Think Injury or Death Will Occur

See #4, based on fact-based medical data this gene-therapy is causing death and injury. Past research on mRNA also shows several risks that have been ignored for this current trial gene-experiment. A 2002 study on SARS-CoV-1 spike proteins showed they cause inflammation, immunopathology, blood clots, and impede Angiotensin 2 expression. This experiment forces the body to produce this spike-protein inheriting all these risks.

Nuremberg Code #6: Risk Should Never Exceed the Benefit

Covid-19 has a 98-99% recovery rate. The vaccine injuries, deaths and adverse side-effects of mRNA gene-therapy far exceed this risk. The use of “leaky” vaccines was banned for agriculture use by the US and EU due to the Marek Chicken study that shows ‘hot-viruses’ and variants emerge… making the disease even more deadly. Yet, this has been ignored for human use by the CDC knowing fully the risk of new deadlier variants emerge from leaky vaccinations. The CDC is fully aware that the use of leaky vaccines facilitates the emergence of hot (deadlier)strains. Yet they’ve ignored this when it comes to human

Nuremberg Code #7: Preparation Must Be Made Against Even Remote Possibility of Injury, Disability or Death

There were no preparations made. This gene therapy skipped animal trials. The pharmaceutical companies’ own Phase 3 human clinical trials will not conclude until 2022 /2023. These vaccines were approved under an Emergency Use only act and forced on a misinformed public. They are NOT FDA-approved.

Nuremberg Code #8: Experiment Must Be Conducted by Scientifically Qualified Persons

Politicians, media and actors claiming that this is a safe and effective vaccine are not qualified. Propaganda is not medical science. Many retail outlets such as Walmart & drive-through vaccine centers are not qualified to administer experimental medical gene-therapies to the uninformed public.

Nuremberg Code #9: Anyone Must Have the Freedom to Bring the Experiment to an End At Any Time

Despite the outcry of over 85,000 doctors, nurses, virologists and epidemiologists – the experiment is not being ended. In fact, there are currently many attempts to change laws in order to force vaccine compliance. This includes mandatory and forced vaccinations. Experimental ‘update’ shots are planned for every 6 months without any recourse to the growing number of deaths and injuries already caused by this experiment. These ‘update’ shots will be administered without any clinical trials. Hopefully this new Nuremberg Trial will put an end to this crime against humanity.

Nuremberg Code #10: The Scientist Must Bring the Experiment to an End At Any Time if There’s Probable Cause of it Resulting in Injury or Death

It is clear in the statistical reporting data that this experiment is resulting in death and injury yet all the politicians, drug companies and so-called experts are not making any attempt to stop this gene-therapy experiment from inflicting harm on a misinformed public.

What can you do to help put an end to this crime against humanity? Share this information. Hold your politicians, media, doctors and nurses accountable – that if they are complicit in this crime against humanity they too are subject to the laws set forth in the Geneva Convention and Nuremberg Code and can be tried, found guilty and put to death. Legal proceedings are moving forward, evidence has been collected and a large growing body of experts are sounding the alarm.

Visit the Covid Committee website at: https://corona-ausschuss.de/ and if you have been affected by this crime, report the event, persons involved, and as much detail to the following website:

https://www.securewhistleblower.com/

Crimes against humanity affect us all. They are a crime against you, your children, your parents, your grandparents, your community and your country and your future.

Judicial Watch Sues for Records of Pentagon Communications about Tucker Carlson and Fox News

Judicial Watch Sues for Records of Pentagon Communications about Tucker Carlson and Fox News

(Washington, DC) – Judicial Watch announced today that it filed a Freedom of Information Act (FOIA) lawsuit against the Department of Defense seeking records of communications between Defense Secretary Lloyd Austin and other top military officials regarding Fox News and its host Tucker Carlson, whose recent commentary on the U.S. military was attacked by top Pentagon officials (Judicial Watch v. U.S. Department of Department of Defense (No. 1:21-cv-01225)).

Judicial Watch filed the lawsuit in the U.S. District Court for the District of Columbia after the Department of Defense failed to reply to a March 16, 2021, FOIA for:

All emails sent between Secretary of Defense Lloyd Austin and email accounts ending in .gov and/or .mil containing the terms “Tucker Carlson” and/or “Fox News.”

All emails sent between Chairman of the Joint Chiefs of Staff Gen. Mark Milley and email accounts ending in .gov and/or .mil containing the terms “Tucker Carlson” and/or “Fox News.”

All emails sent between Vice Chairman of the Joint Chiefs of Staff Gen. John Hyten and email accounts ending in .gov and/or .mil containing the terms “Tucker Carlson” and/or “Fox News.”

The time frame of the request was identified as March 1, 2021 to March 16, 2021.

In the March 9, 2021, broadcast of “Tucker Carlson Tonight,” Carlson said:

So we’ve got new hairstyles and maternity flight suits. Pregnant women are going to fight our wars. It’s a mockery of the U.S. military. Well, China’s military becomes more masculine as it’s assembled the world’s largest navy…. It’s a mockery of the U.S. military.

Pentagon spokesman John Kirby said that Defense Secretary Austin was “revulsed” by Carlson’s comments.

Official military Twitter accounts were also used to attack Carlson’s views.

On his March 11 show, Carlson accused the Pentagon of declaring “war on a domestic news operation:” 

Since when does the Pentagon declare war on a domestic news operation? We can’t remember that ever happening. But we’re going to pass on that, because this is bigger than a feud with some flack at the Pentagon. This is genuinely worrisome.

“Judicial Watch is disturbed about the Pentagon’s illicit secrecy about its coordinated attacks on the First Amendment-protected speech of Tucker Carlson,” stated Judicial Watch President Tom Fitton. “The fact that we must take the Pentagon to federal court for these documents suggests the agency has something to hide.”

Texas Republican Sen. Ted Cruz sent a letter to Defense Secretary Austin demanding a meeting with the Commandant of the Marine Corps to account for the attacks on Carlson and “a plan to prevent other military units from being similarly mobilized against the speech of American citizens.”

In the letter, Sen. Cruz wrote:

I am deeply troubled that the comments you made, and the military’s broader obligation to avoid political endorsements and controversy, are being systematically undermined for the sake of leftwing ideology and political expediency. The last week has witnessed the Pentagon mobilize systematic, public attacks against television host Tucker Carlson that in substance, tone, and political resonance are inexplicably inappropriate.

The Department of Defense has rules about how members of the U.S. military can participate in politics. Active military members may express a personal opinion on political candidates and issues, but they cannot express opinions on behalf of or as a representative of the U.S. military. As Miliary.com stated in 2016:

The DoD’s regulations are guided mostly by the Hatch Act, a federal law passed in 1939 restricting certain types of political activity among military members and other federal employees. The U.S. Office of Special Counsel provided updated “guidance” to the act regarding social media activity in 2012 and again in late 2015.

Source: https://www.judicialwatch.org/press-releases/

Dr. Fauci and the NIH’s History in Experimenting on Foster Children and Using Aborted Fetal Tissue to Develop an HIV Vaccine

Dr. Fauci and the NIH’s History in Experimenting on Foster Children and Using Aborted Fetal Tissue to Develop an HIV Vaccine

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Top row left to right: CDC Director Robert Redfield, Bill Gates, Operation Warp Speed Director Dr. Moncef Slaoui. Bottom row next to President Trump: Dr. Anthony Fauci, and Dr. Deborah Birx. These four doctors and Bill Gates have a history of working together through the NIH to develop an HIV Vaccine, and they are currently working to develop a COVID vaccine.

by Brian Shilhavy
Editor, Health Impact News

When we started MedicalKidnap.com in 2014, one of the shocking things we learned was that it was perfectly legal for medical researchers to use foster children as lab rats to develop drugs. Once the state takes custody of a child away from the parents, and the child becomes a ward of the state, medical researchers no longer need parental approval to conduct medical research, and they can also bill the U.S. Government directly to fund this research, usually using Medicaid, even if the drugs being used are experimental and have not yet been approved by the FDA.

We published an article in May of 2015 highlighting this horrible practice that is legal in the U.S. See:

Medical Kidnapping in the U.S. – Kidnapping Children for Drug Trials

Some highlights from that article:

The U.S. federal government has mandated drug research with children. The need for children to participate in drug company research is high, and the temptation to overstep parental rights to force children to participate is great. Researchers publicly admit using money and other rewards to obtain participation of children in their drug trials.

Organizations that advocate for the rights of parents to make decisions regarding their children’s healthcare are finding that foster children in CPS custody are being enrolled in drug experiments without parental approval. State Child Protective Services are enrolling children in drug experiments without parental approval or court orders. However, those who conduct these drug experiments for pharmaceutical companies, and those who are charged with monitoring such research, do not see a problem with their recruitment methods.

In a 2011 article in the Journal Pediatrics, researchers discussed the problem of recruiting children for participation in clinical trials for drug testing. Researchers from Ohio State University (Columbus) and Case Western Reserve University, confirm that the US federal government is mandating that children be included in clinical research studies.

Dr. Tishler, PhD, and Dr. Staats Reiss, PhD stated:

Since 1994, federal guidelines have called for the inclusion of children in clinical studies. Related federal incentives and laws such as the “pediatric rule” (the Pediatric Research Equity Act) and the pediatric exclusivity provision have also been passed to increase the number of pediatric clinical trials launched by pharmaceutical companies. Despite these mandates, the allocations to pediatric clinical trials in federal and private research and development budgets have remained limited. In addition, pediatric researchers continue to experience difficulty locating children and families who are willing to enroll in clinical trials.

Recruitment for pediatric studies is hampered by several factors including ethical concerns with using children as subjects, regulatory oversight that is significantly more restrictive for child trials than for adult trials, a lack of research infrastructure, the need to obtain consent from parents, and the challenge of determining appropriate payments for participation that are not coercive.

In 2005, a hearing with the title “Protections for Foster Children Enrolled in Clinical Trials” was held by the U.S. House of Representatives. The Subcommittee on Human Resources of the Committee on Ways and Means, investigated whether adequate safeguards were in place to protect foster children from being forced to participate in drug studies.

The allegation that they were investigating involved clinical drug trials on AIDS drugs that were conducted during the period from the late 1980s through 2001.

Since publishing this article back in 2015, much more information has come to surface, especially in light of the COVID Plandemic of 2020. The same group of people who have been involved in HIV/AIDS research to develop an HIV vaccine, a vaccine which has never come to market, are the same group of people now working with the U.S. Government to develop a COVID vaccine.

The public has a right to know more about the past research to develop an HIV vaccine, and how they experimented on children who were “legally” kidnapped from their families for research purposes, as well as the live aborted fetuses that were used to try and create “humanized mice” to produce this vaccine, since this is the same group that has been given hundreds of millions of dollars by the U.S. Government to now develop a COVID vaccine.

Dr. Fauci and the National Institute of Allergy and Infectious Diseases Use of Foster Children in Developing an HIV Vaccine

Faith Dyson recently published an article on Facebook titled: What Was Fauci’s Role In Funding Tuskgegee-Like AIDS Experiments On Foster Children In Seven U.S. States?

She relies heavily on the work of investigative journalist Liam Scheff, and his research published in the book, The House That AIDS Built, which can be found online here.

In 2004 – investigative journalist, Liam Scheff, exposed the fact that hundreds of Foster children at Incarnation Children’s Center [ICC] in NYC were used and abused as lab rats for unsupervised and unrestricted AIDS research and Vaccine studies by Big Pharma and The National Institute of Allergy and Infectious Diseases [NIAID].

Years later in separate investigations – 13,878 children were discovered to have been made subject of the same fate during the 1980’s and 1990’s in six other states: Illinois, Louisiana, Maryland, North Carolina, Colorado and Texas.

Committee on Ways and Means

Phil Crane, right, meets with President George W. Bush and Representative Bill Thomas of Committee on Ways and Means. Image Source.

As we found out in our own investigative report back in 2015, Congress knew about these medical experiments being conducted on foster children and conducted a hearing in 2005, with the title “Protections for Foster Children Enrolled in Clinical Trials.”

The transcript of these hearings used to be on the House.gov website, but since we published our article it has been removed. A copy can be found at Archives.org here.

When the Subcommittee on Human Resources of the Committee on Ways and Means, U.S. House of Representatives met to examine this problem, Chairman Wally Herger, Representative from California made this statement:

Over the last 18 months, this Subcommittee has heard hearings about a number of issues affecting kids in the Federal, State child welfare programs, and this issue is like many of them: It has the potential for being explosive. The child welfare program in the richest, most powerful country in the world is, and has been, often an abysmal failure.

Now, we don’t need proof of more of that. We can give you all kinds of examples of it. We know about kids losing their lives in the child welfare system. Practically every State legislature every year deals with one case or another, and everybody wrings their hands, and the problems go on. The kids are sometimes locked up and sometimes starved under the supervision of the agencies. We know the children have been used without proper supervision for drug testing.  (emphasis added)

The first witness to testify before the House subcommittee was Dr. Donald Young, M.D., U.S. Department of Health and Human Services, Principal Deputy Assistant Secretary for Planning and Evaluation. He provided extensive testimony regarding governmental oversight. Dr. Young concluded his remarks by stating:

We continue to address challenges posed by the threat of HIV/AIDS and are committed to basic and clinical research to strengthen the nation’s ability to cope with this infectious disease. The protection of human subjects, including children, in clinical trials has been and will remain a top priority for HHS. HHS is firmly committed to the protection of the rights and welfare of every individual who participates in human research consistent with sound ethical standards and regulatory requirements.

Later in the hearing, Dr. Young was asked if any changes were needed in regard to foster children and their participation in drug experimentation. Dr. Young stated:

We are not aware of any changes that we believe need to be made. If they are identified, we will be very happy to consider them and make a decision as how best to proceed. We share with you the concern about the adequate protection of foster children. At the same time, the opportunity to let them participate and get the advantage of clinical research, if that is theirs and their guardian’s decision.

It appears that this Congressional hearing, while acknowledging that foster children were being enrolled in HIV/AIDS vaccine trials, did nothing to stop it.

Liam Scheff details what some of these foster children went through in his book.

In New York’s Washington Heights is a 4-story brick building called Incarnation Children’s Center (ICC). This former convent houses a revolving stable of children who’ve been removed from their own homes by the Agency for Child Services [ACS]. These children are black, Hispanic and poor.

Once taken into ICC, the children become subjects of drug trials sponsored by NIAID (National Institute of Allergies and Infectious Disease, a division of the NIH), NICHD (the National Institute of Child Health and Human Development) in conjunction with some of the world’s largest pharmaceutical companies – GlaxoSmithKline, Pfizer, Genentech, Chiron/Biocine and others.

The drugs being given to the children are toxic – they’re known to cause genetic mutation, organ failure, bone marrow death, bodily deformations, brain damage and fatal skin disorders.

If the children refuse the drugs, they’re held down and have them force fed. If the children continue to resist, they’re taken to Columbia Presbyterian hospital where a surgeon puts a plastic tube through their abdominal wall into their stomachs. From then on, the drugs are injected directly into their intestines.

In 2003, two children, ages 6 and 12, had debilitating strokes due to drug toxicities. The 6-year-old went blind. They both died shortly after.  Another 14-year old died recently. An 8-year-old boy had two plastic surgeries to remove large, fatty, drug-induced lumps from his neck.

This isn’t science fiction. This is AIDS research. The children at ICC were born to mothers who tested HIV positive, or who themselves tested positive. However, neither parents nor children were told a crucial fact — HIV tests are extremely inaccurate. The HIV test cross-reacts with nearly seventy commonly-occurring conditions, giving false positive results. These conditions include common colds, herpes, hepatitis, tuberculosis, drug abuse, inoculations and most troublingly, current and prior pregnancy. This is a double inaccuracy, because the factors that cause false positives in pregnant mothers can be passed to their children – who are given the same false diagnosis.

Most of us have never heard this before. It’s undoubtedly the biggest secret in medicine. However, it’s well known among HIV researchers that HIV tests are extremely inaccurate – but the researchers don’t tell the doctors, and they certainly don’t tell the children at ICC, who serve as test animals for the next generation of AIDS drugs. ICC is run by Columbia University’s Presbyterian Hospital in affiliation with Catholic Home Charities through the Archdiocese of New York.

Does the issue of “inaccurate tests” sound familiar? It should, because we are seeing the exact same thing today with COVID tests.

Faith Dyson writes about her reaction after reading Liam Scheff’s reports:

When I read the report, I was much like the general public – totally ignorant of NIAID; its director, funding, etc. and I doubt at that time there were very many other people who would have known who was in charge of the Agency outside of government bureaucrats, scientists, researchers, activists and possibly those who were affected by ‘the AIDS/HIV virus’.

What’s interesting to note here is that the source and/or existence of that pandemic is another highly questionable subject, because it appears to mimic the same scenario that accompanies the latest super-bug to attack the world’s population, the Coronavirus.

In fact – they’re so much alike, one would think the exact same plan had been followed in the production of both epidemics; the older one, AIDS/HIV, using monkeys and the newer one, Corona, using bats. (See link #3 for a shocking revelation re: active viruses in childhood vaccines that cause AIDS, Cancer, and Leukemia plus a host of other diseases and disorders and see #4 for the traumatic details of how the effects are still plaguing our population decades later.)

Therefore – due to the results of the AIDS/HIV epidemic, those most affected by it had been demanding – from the same government Agency and pharmaceutical companies – some sort of treatment, vaccine, drug, etc. to stem the tide of the infection.

So the big question back then was:

“Where could Big Pharma and NIAID find lab rats to whom they could offer ‘free medical care’ in the guise of ‘helping to prevent and/or remedy their suffering’ all the while using them in AIDS/HIV drug and vaccine trails – without being bothered from outside interference, the same as was done in the infamous Tuskgegee Syphilis Experiment?” (See link #5.)

As Liam Scheff uncovered – the answer to their mad scientific prayers was the unsupervised and unprotected wards of the state, a.k.a. ‘Foster children’.

However – since the newest pandemic has arisen to overshadow all others, and we now have a much larger group of people demanding the same provisions from the same corporations and Government Agency, we all know who is the head of NIAID.

It’s Dr. Anthony Fauci, one of the lead members of the Trump Administration’s White House Coronavirus Task Force addressing the COVID-19 pandemic in the United States.

So a recap of the facts we’ve learned from the corona outbreak – in conjunction with the AIDS/HIV funding that spawned the experiments at Incarnation Children’s Center and elsewhere – are as follows:

1) Dr. Fauci has been the director of NIAID, a division of The Executive Branch of The U.S. Government, since 1984, so he was also director during the Incarnation Children’s Center Experiments,

2) his NIAID profile states that he still currently “oversees an extensive research portfolio of basic and applied research to prevent, diagnose, and treat established infectious diseases such as HIV/AIDS, respiratory infections, diarrheal diseases, tuberculosis and malaria as well as emerging diseases such as Ebola and Zika.” (See link #6),

3) Fauci participates in Gate-sponsored Global Health Conferences and is listed on The Leadership Council for The Bill And Melinda Gates Foundation (See link #7 and #8.), which has a huge stake in the profits from a Vaccine, Contact Tracing, microchipping, and various other technologies,

4) NIAID illegally outsourced $3.7 Million in U.S. Tax-payer’s money to Chinese scientists in the Wuhan Lab at the center of the Coronavirus outbreak for researching its ‘gain of function’ – after a moratorium had called a halt to all U.S. involvement in such studies. (See link #9.)
and,

5) Fauci famously predicted in a speech from 2017 at Georgetown University: “[…], but also there will be a surprise outbreak […], and the history of the last 32 years that I’ve been the director of NIAID will tell the next administration that there’s no doubt in anyone’s mind that they will be faced with the challenges that their predecessors were faced with” – in a battle with a pandemic of infectious disease. (See link #10)

Read the entire article by Faith Dyson here.

Judicial Watch Sues the FDA to Obtain Records on Purchases of “Fresh and Never Frozen” Fetus Parts for HIV/AIDS Research

Last week we published an interview between Robert F. Kennedy, Jr. and Dr. Theresa Deisher regarding the use of human fetal tissue to culture viruses for vaccines.

Most of the COVID vaccines being developed are using human fetal tissue to culture the coronavirus.

One of the more interesting questions Mr. Kennedy asked Dr. Deisher was why the manufacturers of vaccines switched from exclusively using animal tissue to culture viruses for vaccines, to start using aborted fetal tissue some years back.

Dr. Deisher’s reply was that the industry was getting a lot of pressure from the animal rights movement to stop using animals for experimentation.

Mr. Kennedy was shocked, and stated:

It’s kind of weird to think that the animal rights activists have more clout with the vaccine companies than do the anti-abortion activists.

Dr. Deisher replied:

They do. And you know what’s really alarming is the lack of outcry over human babies born alive at five to six months old so that their hearts can be obtained beating. And they have to be beating to be used in the research that’s being done.

If the heart has stopped beating, it’s not useful. You cannot use it.

And so these babies are delivered alive, and their hearts cut out without anesthesia.

I wouldn’t do that to a mouse….

Watch the interview here.

Earlier this week, June 23, 2020, Judicial Watch announced that they had obtained records showing that the FDA paid for “Fresh and Never Frozen” human fetal parts for use in “Humanized Mice” creation in the past for HIV/AIDS research.

Judicial Watch announced today it received 165 pages of records from the Food and Drug Administration (FDA) showing the FDA between 2012 and 2018 entered into 8 contracts worth $96,370 with Advanced Bioscience Resources (ABR) to acquire “fresh and never frozen” tissue from 1st and 2nd trimester aborted fetuses for use in creating “humanized mice” for ongoing research.

ABR is a non-profit firm which has been the subject of criminal referrals from House and Senate committees investigating whether Planned Parenthood or any other entity was illegally profiting from the handling of fetal tissue from aborted babies.

Judicial Watch filed the lawsuit in the United States District Court for the District of Columbia (Judicial Watch v. U.S. Department Health and Human Services (No. 1:19-cv-00876)) after HHS failed to respond adequately to a September 28, 2018, FOIA request seeking:

  1. All contracts and related documentation between FDA and Advanced Biosciences Resources (ABR) for the provision of human fetal tissue to be used in humanized mice research.
  2. All records reflecting the disbursement of funds to ABR for the provision of human fetal tissue to be used in humanized mice research.
  1. All guidelines and procedural documents provided to ABR by FDA relating to the acquisition and extraction of human fetal tissue for its provision to the FDA for humanized mice research.
  2. All communications between FDA officials and employees and representatives of ABR related to the provision by ABR to the FDA of human fetal tissue for the purpose of humanized mice research.

The lawsuit can be read here.

On February 13, 2020, Judicial Watch announced:

(Washington, DC) – Judicial Watch announced it received 676 pages of records from the National Institutes of Health (NIH) showing that the agency paid thousands of dollars to a California-based firm to purchase organs from aborted human fetuses to create “humanized mice” for HIV research.

The records show that NIH paid at least $18,100 between December 2016 and August 2018 to Advanced Bioscience Resources (ABR) for livers and thymuses from second trimester aborted fetuses. They include at least 26 such purchases from ABR by Dr. Kim Hasenkrug, senior investigator at the NIH lab in Hamilton, Montana.

Purchase orders associated with the transactions state: “These tissues, liver and thymus, are required [by] Ron Messer for ongoing studies of HIV in the Hasenkrug Lab. Our mice will be ready for reconstitution soon.”

The Trump Administration put a ban on using aborted human fetal tissue in federally funded research, but during the COVID Plandemic some members of Congress petitioned to get an exemption for COVID-19 research. (Source.)

HIV/AIDS DNA Vaccine now a COVID DNA Vaccine Project – Same People, Same Methods

Having failed at their attempts to develop a DNA altering vaccine for HIV/AIDS, the same group of people are now collecting BILLIONS of dollars of U.S. funding to develop a COVID DNA altering vaccine.

It looks a lot like the same play book, only this time it is on “Warp Speed” for fast-tracking, and instead of using fresh fetal tissue to create “humanized mice” they have the FDA’s approval to conduct trials directly on humans, with no animal testing first.

What will be the results?

See Also:

Unmasking Who is Behind the Plandemic and Rioting to Usher in the New World Order

7 Billion Doses of COVID-19 Vaccine for World’s Population of 7 Billion – Was This the Plan All Along?

Dr. Judy Mikovits and Dr. Sherri Tenpenny: A New COVID Vaccine Could Kill 50 Million People in the U.S.

Copyright 2020 Health Impact News. Free to republish using Creative Common standards with correct author attribution and links back to this original article.

Tucker Calls for Criminal Probe of Fauci… Videos

Tucker Calls for Criminal Probe of Fauci…

Posted on by Soren Dreier
Author: Tucker May 15, 2021