CHD’s New ‘Medical Racism’ Film Exposes Long-Standing Experimentation on Minorities
Watch the trailer now! Medical Racism, premiering March 11, chronicles the medical cartel’s history of targeting minorities for unethical experiments, the acquiescence of regulatory agencies and medical ethicists, and the silence of physicians who allow these atrocities to continue today.
Children’s Health Defense, in conjunction with Centner Productions and the Urban Global Health Alliance, along with co-producers Rev. Tony Muhammad and author-historian Curtis Cost, today released the trailer for their upcoming documentary, “Medical Racism: The New Apartheid.”
“Medical Racism,” which premieres March 11, illuminates the shocking history of government health regulators and private pharmaceutical companies conducting human experiments on Black Americans.
“Though many Americans are familiar with the history of medical atrocities committed by the Centers for Disease Control and Prevention at Tuskegee, by the father of American gynecology, Dr. J. Marion Sims, on South Carolina slave girls and the continuing medical larceny against Henrietta Lacks, most people are likely unaware of the routine medical barbarism committed against Africans that persists today,” said Curtis Cost, the film’s co-producer.
The documentary, directed by Academy Award nominee David Massey, chronicles the medical cartel’s long history of targeting minority populations for unethical experiments, the acquiescence of regulatory agencies and medical ethicists, and the silence of physicians who allow these atrocities to continue today.
According to “Medical Racism” producer Kevin Jenkins of the Urban Global Health Alliance: “These racially targeted experiments have been hiding in plain sight for decades. It’s time to expose the truth and end inhumane and barbaric forms of racism by the ‘respected’ medical establishment.”
“Medical Racism” explores the recent racially based experimentation by government health officials and pharmaceutical companies on Black children in South Central Los Angeles.
The film also exposes Big Pharma’s medical experiments and “drug dumping” in modern-day Africa, and the World Health Organization’s 2014 population control campaign to sterilize a million Kenyan girls with infertility chemicals hidden in tetanus vaccines.
“The high levels of medical mistrust in the Black community are a rational response to routine callousness and systemic savagery toward Blacks by medical professionals and pharmaceutical interests,” said Robert F. Kennedy, Jr., chairman of Children’s Health Defense. “Our hope in producing this film is to learn from past misdeeds, so we can avoid their future repetition.”
For more information and to register to receive a notification on where and how the film can be seen when it’s released, visit medicalracism.org.
Whopper-doozie alert! This one is so over the top that I simply had to blog about it. It was shared by W.G., whom I thank for bringing to my attention. To be honest, this is such a whopper-doozie that I don’t even know where to start with respect to today’s high octane speculation, and I rather suspect – once readers dive into the article – that it will stimulate your own speculations. I’m presenting three different sources or versions of this story, because it is so unbelievably breathtaking in its implications:
Let’s look at the second article linked above. Consider these breathtaking paragraphs:
Pfizer has been accused of “bullying” Latin American governments in Covid vaccine negotiations and has asked some countries to put up sovereign assets, such as embassy buildings and military bases, as a guarantee against the cost of any future legal cases, the Bureau of Investigative Journalism can reveal.
In the case of one country, demands made by the pharmaceutical giant led to a three-month delay in a vaccine deal being agreed. For Argentina and Brazil, no national deals were agreed at all. Any hold-up in countries receiving vaccines means more people contracting Covid-19 and potentially dying.
Officials from Argentina and the other Latin American country, which cannot be named as it has signed a confidentiality agreement with Pfizer, said the company’s negotiators demanded additional indemnity against any civil claims citizens might file if they experienced adverse effects after being inoculated. In Argentina and Brazil, Pfizer asked for sovereign assets to be put up as collateral for any future legal costs.
One official who was present in the unnamed country’s negotiations described Pfizer’s demands as “high-level bullying” and said the government felt like it was being “held to ransom” in order to access life-saving vaccines. (Boldface emphasis added)
That pretty much sums it up; “Muck Pharmaceuticals” as we like to call Big Pharma here, in the form of Pfizer, is allegedly demanding collateral against potential lawsuits against its “vaccine.” Now my high octane speculation of the day comes in the form of three questions: (1) Why would Pfizer be so concerned about potential lawsuits if it was confident its “vaccine” was safe? (2) why would it ask nations for embassies and military bases? And (3) was the idea of collateralizing embassies and military bases the objective of the planscamdemic/”vaccine” operation one of the goals at the outset of the whole planscamdemic to begin with?
In looking at question one, we gain a bit of a speculative clue: seizing a nation’s embassies and military bases is, from one point of view, a real estate scam, one which anticipates that lawsuits are likely to be both many and costly, which is in its way a tacit admission that there are “problems” with the “vaccines.” The amounts of money are likely to be vast, and thus, hard assets are required in order to minimize Muck Pharmaceutical’s exposure to the risk.
But that brings us to question two: why ask for embassies and military bases? This, in my opinion, means one of two things, and possibly both together: either Pfizer’s action is on behalf of someone else whom it anticipates can buy those assets – and has the money to do so – should lawsuits ensue, or Pfizer itself views itself as a sovereign entity, in need of embassies and military bases to enforce its corporate will, which implies its having plans for a professional corporate military, or its has already developed one. Or, as I already stated, it is some combination of these two. With regard to the first prospect, there are few actors on the world stage that would have the liquidity to buy such hard assets, and use them for their original intended purpose. China would certainly be one primary suspect, and after all, the planscamdemic did originate there in a certain sense. But there could be others as well, including extra-territorial actors.
And that leads us to question three: was this one of the goals (among many others) that Mr. Globaloney wanted to accomplish through the planscamdemic? I suspect it’s a strong possibility, since it is clear that Mr. Globaloney is using the whole farce to further his agenda of control. And control doesn’t work unless one has centers for intelligence operations that are “sovereign territory” (embassies) and a means to enforce its dictates (military bases).
When one considers that there are other effective methods of covid treatment, this draconian effort regarding vaccines seems to make the agenda all too obvious.
(Please note that I have excerpted a good deal of the text which is available at the link below)
Sausage Making at FDA: How Human Cancer Cells Got Into Vaccines
In a 2012 meeting, the FDA voted to allow the use of human fetal cells and adult human tumor cells in vaccines, despite acknowledging the many risks, including that vaccine recipients might later develop cancer.
“If the American people knew some of the things that went on at the FDA, they’d never take anything but Bayer aspirin.” — Len Lutwalk, FDA scientist
“The FDA, by spinelessly knuckling under to every whim of the drug companies, has thrown away its high reputation, and in doing so, forfeited our trust.” — Drummond Rennie, deputy editor of JAMA
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Vaccines and related biological products advisory committee today
Today — Thursday, Dec. 10 — the Vaccines and Related Biological Products Advisory Committee (VRBPAC), which is the U.S. Food and Drug Administration’s (FDA) internal panel that licenses new vaccines as “safe and effective,” will meet to consider Pfizer’s COVID vaccine. VRBAC will meet in one week, Dec. 17, to consider approval of the Moderna vaccine.
The damning safety studies in Pfizer’s late release clinical trial data dump, and the severe (life-threatening) allergic reactions that bedeviled the vaccine’s UK rollout, have raised red flags and public anxiety about the safety of the companies’ mRNA vaccines. Anthony Fauci has addressed growing skepticism about COVID vaccines and the Operation Warp Speed program, by reassuring the public that “VRBPAC” is an “independent panel of leading experts” whom the public can absolutely trust to assure vaccine safety.
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How FDA originally approved use of fetal cells in vaccines
FDA allows both human fetal cells and adult human tumor cells in vaccines. Both types have cancer risks. While both Pfizer and Moderna tested their mRNA vaccine using fetal cells, there are no fetal cells, cell debris or DNA in their final products.
However, according to company documents, Johnson and Johnson (Janssen) and Altimmune’s COVID vaccines are manufactured in the human fetal cell line PER-C6, and thus the final vaccine products will contain cellular debris and DNA fragments from these cells. Researchers harvested these cell lines from the eyeball of an 18-week-old human fetus aborted in 1985, and then rendered them immortal by making them cancerous.
The AstraZeneca, Cansino, Gamayela, Vaxart, LongComm and Upitt vaccines are manufactured in the human fetal cell line HEK293, and thus the final vaccine products will contain cellular debris and DNA fragments from the fetal HEK-293 cell line. Scientists harvested this cell line from the kidney of a female Dutch fetus legally aborted in 1973 and then immortalized the cells by rendering them cancerous.
Normal primary cells, which are unable to replicate indefinitely, ultimately die. Immortalized cell lines are derived from known malignant cancer cells such as those obtained from Henrietta Lacks (HeLa) or created in the laboratory by introducing viral oncogenes or chemical exposures capable of mutating normal primary cells into immortal tumor cells.
According to FDA’s “The Pink Sheet” dated Nov. 29, 1999, for two decades the agency has been acutely aware of the inherent risks of using immortalized cell lines for vaccine development. The FDA CBER Director Dr. Peter Patriarca, M.D. explained that continuous cell lines are used for their ability to self-propagate, making them an ideal substrate on which to grow viruses, “the worst thing we are concerned about is … malignancy, because some of these continuous cells have the potential for growing tumors in laboratory animals.”
Patriarca further conceded that “the technology to make these vaccines actually exceeds the science and technology to understand how these vaccines work and to predict how they will work.” …
We call vaccines “biologics” because vaccinologists have traditionally grown their antigens on biological substrates — usually animal tissue. Competing companies culture COVID vaccines on a variety of animal strata. The Merck and IAVA COVID vaccines are manufactured in vero monkey cells, and thus contain cellular debris and DNA fragments from vero monkeys in the final product. The Sanofi, GSK, and Novavax COVID jabs are manufactured in insect cells and thus contain insect cellular debris and DNA fragments in the final products.
Public health advocates criticize the use of animal tissues in vaccines due to risks that they carry endogenous viruses, microbes, parasites and lack safety testing. (Plague of Corruption, Mikovits 2020). …
Researchers and regulatory agencies have worried for more than 50 years about the potential for injected DNA to cause cancer. …
Regulators have in the past predicted that the odds of that happening were less than 1 in a trillion. However, in early gene therapy trials this event did indeed occur in 4 of 9 boys, 1 of whom died from the leukemia the insertions caused.
But as corrupt as FDA is, the internal panels — VRBAC — that approve new vaccines make the rest of the agency look like a Sunday church picnic.
When Dr. Fauci, Paul Offit, Peter Hotez and Bill Gates tell you that you needn’t worry because FDA is the “gold standard” for vaccine safety and that the ultimate licensing decision will be made by an “independent panel of experts,” they are talking about VRBPAC. But VRBPAC is far from “independent.” It is not even comprised exclusively of public officials. Instead, it is populated by outside “experts” who are almost all pharmaceutical industry insiders.
In 2003, following a 3-year investigation, the United States Congress’s House Oversight Committee found VRBAC was completely dominated by the vaccine industry.
“Examples of Conflicts of Interest:
“For instance, 3 out of 5 FDA advisory committee (VRBPAC) members who voted to approve the rotavirus vaccine in December 1997 had financial ties to pharmaceutical companies that were developing different versions of the vaccine.
“One out of five voting members’ employer had a $9,586,000 contract for a rotavirus vaccine.
“One out of five voting members was the principal investigator for a Merck grant to develop a rotavirus vaccine.
“One out of five voting members received approximately $1 million from vaccine manufacturers toward vaccine development.”
Congressional investigators concluded that, “Altogether, four out of the five committee members had conflicts of interest that required waivers, and their recommendation for approval of the vaccine was unanimous.”
Here’s what happened at the 2012 FDA meeting on fetal cells
HHS acknowledges that the FDA and Centers for Disease Control committees that contract and review new vaccines have historically not used “evidence-based medicine.” To illustrate what this means, one only need read (below) the astonishing transcript of the 2012 panel that first approved the use of adult cancer tumor cells in vaccines.
This transcript shows what the public is never supposed to see: the behind-the-scenes sausage-making of federal vaccine approvals. Here, you will read for yourself how the “independent,” “gold standard” panelists entrusted with protecting your children made monumentally consequential decisions, not on evidence-based science, but by rolling the dice and taking what they knew was a horrendously risky bet on public health
In any other realm, this transcript would be proof of negligent homicide. … We are all lab rats in their high-risk population-wide experiment. At FDA’s vaccine division, that sort of reckless decision-making is routine.
In 2012, most live virus vaccines were from animal tissue and the idea of putting potentially cancerous tumor cells from adult “donors” in vaccines was still a daring and audacious gamble. That September, the FDA VRBPAC committee met to discuss this risky innovation. The transcript of that meeting — showing captive FDA officials considering a proposal by the pharma cabal to allow the use of human cancer cells (HeLa) to replace animal tissue in the manufacture of vaccines — is proof of reckless criminal conduct.
Unbelievably, FDA voted to allow pharmaceutical companies to produce vaccines using human cells without reviewing a single scientific study to determine if the outcome would be safe.
Before, I quoted some of the criminally reckless statements from the meeting directly. A more detailed account appears in this article.
This was a full meeting of FDA’s VRBPAC in 2012 to decide on the use of human tumor cell lines for the production of vaccines. I list these speakers and their titles at that time:
Dr. Philip Krause, Acting Deputy Director of OVRR (Office of Vaccine Research and Review) and FDA’s CBER (Center for Biologics Evaluation and Research). Also, Principal Investigator for Vaccine Safety: Virus Detection and Latency.
Dr. Doug Lowy, Director of the National Cancer Institute of the NIH.
Dr. Robert Daum, Chair of the VRBPAC.
Donald W. Jehn M.S., Designated Federal Officer for VRBPAC.
Keith Peden, PhD, Chief of LDNAV, DVP/OVRR/CBER.
Dr. Marion Gruber, Director of the FDA’s Office of Vaccines.
Dr. Nathanial Brady, a self-described clinician.
Dr. Pamela McInnes, a vaccine development expert and the Director of the Division of Extramural Research at the NIH’s National Institute of Dental and Craniofacial Research, and previously a Deputy Director under Anthony Fauci at the National Institute of Allergy and Infectious Diseases.
Pharma knew that their tumorigenic vaccines might cause tumors in recipients.
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FDA officials knew that tumors might occur decades after vaccination.
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FDA openly acknowledged that its primary objective was not to assure public safety but to help vaccine manufacturers.
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FDA officials knew that they could not prove vaccine safety using test animals to assess oncogenicity.
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FDA officials deliberately terminated animal safety tests too early in order to conceal consequences.
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FDA decided to keep the tumor cell lines secret, because doctors and the public may be alarmed and say “Oh, my God!” if they knew the truth.
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FDA decided to use deceptive language to convince doctors and the public that the vaccines were safe even when they, themselves, were unconvinced of safety.
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FDA decided to hide information about their use of tumor cells and omit it from package inserts.
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Health authorities were skeptical about safety of the tumor lines, but they decided to subject the public to the risk, so that they could perform a global population-wide live human experiment.
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FDA officials opted to toss the dice, perform the population-wide human experiment, and learn about the risks as time goes by.
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The committee formally approves the method of making vaccines from human cancer tumors.
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Prior to voting to go forward, the committee made the following conclusions:
Making vaccines with cells that are directly derived from human cancer tumors is faster and cheaper than breeding animals for the culture media.
Millions of potentially cancer-causing vaccines will be produced.
The vaccines may possibly cause genetic mutations.
Millions of dollars will be made by vaccine promoters.
The health of millions of consumers may be jeopardized.
Information about how vaccines are made will be hidden from doctors and
Finally, it’s worth considering that cancer treatment drugs like Keytruda are among pharmaceutical companies’ largest profit makers. Precipitating a cancer epidemic in human populations only benefits vaccine makers’ bottom line.
Remember, these are the same companies and the same FDA regulators that brought us the opioid epidemic.
Americans have been following COVID-19 vaccine trial developments for weeks, watching companies jockey for frontrunner status like contestants in a reality TV show. And though participants in some of the studies (by Moderna, Oxford, Johnson & Johnson and Pfizer) have surfaced with reactions serious enough to pause several of the trials, market analysts remain “bullish” about the near-term prospects for approval of these liability-free products by the U.S. Food and Drug Administration (FDA).
On Oct. 16, Pfizer’s CEO indicated the company would likely file for FDA Emergency Use Authorization for its experimental BNT162b2 vaccine in late November. That statement came three days after Pfizer announced that it had received FDA permission to administer the unproven vaccine to children as young as 12, becoming the first company in the U.S. to include young participants in Phase 3 trials. In the UK, Oxford and AstraZeneca gained approval to test their vaccine in children aged 5-12 back in May, a couple of months before two of their adult clinical trial participants developed transverse myelitis.
To date, Pfizer has administered two doses of vaccine to almost 35,000 adult participants in five countries. Unworried by the dramatic side effects reported by some of these adults — including high fever, pounding headaches, body aches, exhaustion and shivering intense enough to crack teeth — more than 90 parents have already expressed interest in volunteering their teenagers.
Are these parents (perhaps left unemployed by coronavirus restrictions) tempted by the financial incentives offered to clinical trial participants, reportedly anywhere from $1200 to $2000? Otherwise, their motivation for wanting to throw their children into the experimental fray is unclear; as the director of the Cincinnati Children’s Hospital stated, “most of the time, what a coronavirus causes is a cold” that does not even make children “sick enough to where a parent says they need to go to a doctor.”
The Cincinnati physician has, nonetheless, just started giving Pfizer’s shot to 16- and 17-year-olds (and soon to 12-15-year-olds). To entice additional young participants, he tells parents that the COVID-19 death rate in children is “not zero” — but declines to spell out that, according to the Centers for Disease Control and Prevention, the survival rate in those age 19 and under is 99.997%. Using similarly vague language, a Memorial Sloan-Kettering health policy expert said that a COVID-19 vaccine’s benefits for the young would likely be “secondary’ in nature” but characterized the gesture as “an act of service to help protect others.”
However, reports in Pediatrics and other journals assert that children are not a source of infection and are far more likely to acquire COVID-19 from adults “rather than transmitting it to them.” In other words, policymakers expect children to accept a risk-benefit equation heavily tilted toward risk.
Corporate bad guy
Pharmaceutical giant Pfizer — the second-largest drug and biotech company in the world and the fourth-highest earner of vaccine revenues — has seen a 7% increase in its share value this year. However, though Pfizer claims to be a standard-bearer for “quality, safety and value,” it has a corporate rap sheet a mile long. Pfizer is routinely mired in controversies involving alleged price-fixing, bribery, kickbacks, tax avoidance, regulatory misdirection and other unsavory practices and has also repeatedly paid fines for environmental violations at its research and manufacturing plants.
Critics point to decades of aggressive and questionable marketing. In 2009, this behavior earned Pfizer the dubious distinction of paying the largest-ever criminal fine at the time — $2.3 billion — for fraudulent and illegal promotion of four drugs, including a painkiller marketed at “dangerously high” doses. In 2016, a British regulator levied a $106 million fine against Pfizer for a 2600% increase in the price of a widely prescribed anti-epilepsy drug that increased the National Health Services’ expenditures from one year to the next — for a single drug—from $2.5 million to $63 million.
Perhaps to compensate for its unpleasant track record, Pfizer is the top drug company spender in state elections, even outspending the industry’s own lobbying group, Pharmaceutical Research and Manufacturers of America (PhRM). As a just-published analysis of drug company political spending by STAT and the National Institute on Money and Politics shows, Pfizer’s “prolific” state-level spending ($778,000 since January 2019) “mirrors its behavior at the federal level, where its [political action committee] was also the top political spender among drug companies” — roughly $1 million over the same time period. The report pointedly notes that while the amounts paid out to legislators represent a “pittance” for a company earning tens of billions a year, “those small chunks of corporate change can have a significant impact.”
Pfizer’s vaccines
Pfizer is responsible for two vaccines on the U.S. childhood and adolescent vaccine schedule: the pneumococcal vaccine Prevnar-13 (given to children under 5 and also to older adults) and the meningococcal vaccine Trumenba (approved for 10 – 25-year-olds). Package inserts link the two vaccines to a large number of serious adverse events, including anaphylaxis and other allergic reactions, severe headaches and chronic muscle and joint pain. Among the roughly 40 harms listed in the Prevnar-13 insert are sudden infant death syndrome (SIDS) and half a dozen other fatal outcomes.
Pfizer developed its COVID-19 vaccine — which uses experimental messenger RNA (mRNA) technology — in partnership with the German biopharma company BioNTech. Although mRNA vaccines must be stored in special ultra-low-temperature freezers that pose certain logistic obstacles, Pfizer is gung-ho on the never-before-approved approach because it bypasses the more costly and difficult methods used in traditional vaccine production. It does this by essentially turning recipients into “vaccine factories” — with long-term risks that are unknown.
Pfizer and BioNTech brought their COVID-19 vaccine candidates “from concept into clinical development” in under three months, perhaps helped along by the current Pfizer CEO’s efforts to restructure Pfizer into a more “nimble” company. At the same time, observers who now place Pfizer at the head of the pack for COVID-19 vaccines credit the company’s “well-oiled system,” remarking that “Pfizer’s incredibly organized and is always … a couple steps ahead, planning where they want to go.”
Conflicts of interest and revolving doors
In the summer of 2019, after having served as the Trump administration’s FDA commissioner for two years, Scott Gottlieb passed through the revolving door to join Pfizer’s board of directors as well as becoming a regular contributor on CNBC. For the past four decades, stepping onto pharmaceutical boards has been par for the course for departing FDA commissioners, though Gottlieb may have upped the ante by also joining the boards of the AI- and big-data-reliant genetic testing start-up, Tempus, and the biotech company Illumina.
While at the FDA, Gottlieb presided over a record number of drug approvals. According to one commentator, this “trail-blazing” FDA stint and Gottlieb’s focus on “hustling up the [drug approval] process … helped endear him to the industry, making him one of the most popular commissioners in FDA history.” As the director of a consumer watchdog group put it, “He’s basically been a shill for pharmaceutical corporations for much of his career.” Two months before stepping down from the agency, Gottlieb attracted notice when he strongly denied any link between vaccines and autism while publicly threatening that the federal government might be “forced” to intervene in states with vaccine exemptions to make vaccines mandatory across the board.
Gottlieb’s affiliation with CNBC may explain why he has been a frequent public face during the coronavirus pandemic, promoting the U.S. as a world leader in the vaccine race but also vocally endorsing measures like universal masking, universal testing and restaurant and school shutdowns. On October 19, Gottlieb dourly told Americans that the U.S. is “entering a pretty difficult period” and that “the hardest part is probably [still] ahead.” Ironically, around the same time that Gottlieb was using positive test results to hype ongoing restrictive measures, a former Pfizer vice-president and chief science officer in the UK characterized mass testing as “inappropriate,” asserting that “it is impossible for the positives to be much other than false.” Discussing the harsh policies that have been particularly disastrous for children, the former Pfizer executive agreed that they have essentially been based on “completely fake data.”
Kids at risk
Reporter Whitney Webb recently outlined how Operation Warp Speed is awarding contracts to vaccine companies through a nongovernmental defense contractor intermediary, a tactic that shields the contracts from oversight and federal regulation. Meanwhile, Moncef Slaoui — who heads up the Operation Warp Speed initiative — stated that after a round of testing in adolescents, he expects the leading coronavirus vaccines to also be tested in toddlers and babies. Parents would do well to keep their children on the sidelines of these experiments. If vaccine clinical trials, including Pfizer’s, are already generating concerning results in adults capable of describing their symptoms, what will happen when preverbal babies experience similar adverse outcomes?
People around the world are watching as U.K. Judge Vanessa Baraitser hears arguments and decides whether or not to extradite Wikileaks Founder Julian Assange to the U.S.
While the Obama administration chose not to charge Assange, wary of the precedent it might set in criminalizing journalism, the Trump administration indicted him with 18 criminal charges that may land Assange in one of the U.S.’s most notorious prisons for 175 years.
Assange’s Wikileaks has won numerous journalism awards and has never had to retract a single publication despite releasing more than 10 million documents exposing, among other things, U.S. war crimes. Former CIA Director Leon Panetta recently indicated that the ongoingpersecution of Assange is meant to “send a message to others not to do the same thing.”
As the world debates whether Assange is a hero or a traitor, Children’s Health Defense takes a step back to examine some of the things his organization has revealed for those fighting for health and environmental justice.
1. U.S. diplomatic efforts to overturn resistance to GMOs at the behest of Monsanto
Wikileaks published hundreds of diplomatic cables exhibiting attempts by the U.S. to quell opposition to genetically modified organisms or GMOs. As reported by The Guardian, “the cables show U.S. diplomats working directly for GM companies such as Monsanto.”
In a 2007 cable, Craig Stapleton, then U.S. Ambassador to France, advised the U.S. to prepare for economic war with countries unwilling to introduce Monsanto’s GM corn seeds. He recommended the U.S. “calibrate a target retaliation list that causes some pain across the E.U.”
Another dispatch, this one from 2009, demonstrated that the U.S. funded a GMO workshop in Mozambique that, according to the authors, helped advance biotech-friendly policies in the country.
In another cable from 2009, a U.S. diplomat stationed in Germany relayed intelligence on Bavarian political parties to several U.S. federal agencies and the U.S. Secretary of Defense, telling them which parties opposed Monsanto’s M810 corn seed and tactics that the U.S. could impose to resolve the opposition.
One cable from Hong Kong shows a State Department employee requesting $92,000 in U.S. public funds for “media education kits” to combat a growing popular movement calling for the labeling of GMO foods in Hong Kong. The cable indicates a desire to “make it much more difficult for mandatory labelling advocates to prevail.” The State Department’s Anita Katial, who wrote the cable, also recalled a time when her office facilitated the sending of pro-biotech and bio-agriculture DVDs to every high school in Hong Kong.
According to Food & Water Watch Executive Director Wenonah Hauter, the trove of cables “really gets down to twisting the arms of countries and working to undermine local democratic movements that may be opposed to biotech crops, and pressuring foreign governments to also reduce the oversight of biotech crops.”
2. Multinational commodities trader dumping toxic waste in West Africa
In 2006, Trafigura, the world’s second largest oil trader, illegally discharged more than 500 tons of highly toxic oil waste near the Port of Abidjan in the Ivory Coast. Some of the dump sites were near agriculture fields or water supplies, and the UN estimates that more than 100,000 people sought medical treatment due to the incident. Wikileaks would later call this incident “possibly the most culpable mass contamination incident since Bhopal.”
Trafigura’s lawyer commissioned a confidential study that listed what the environmental and health impacts of the dumping incident would be after people living near the port started flooding hospitals.
The report explained that contact with the offloaded compounds could lead to eye damage, lung damage, skin burns, headaches, breathing difficulty, permanent skin ulceration, coma and death. The report also states that the chemical compounds would have a “severe and negative effect” on the environment.
As recently as 2016, residents were complaining about the smell of the waste, headaches, breathing problems and skin problems.
Wikileaks published the classified report in 2009, the first time the public could see the company’s true negligence.
3. Gates Foundation sees environmental activists as a threat
In 2008, Bill & Melinda Gates Foundation hired an intelligence firm called Stratfor to put together a “threat assessment report” and determine current and future threats to the foundation.
Stratfor’s report saw environmental activists, indigenous farming groups, and peasant political parties in Asia and South America, as “potential threats” to the foundation.
“Threats to the foundation are likely to be directly related to the public association between the foundation and a controversial issue such as GMOs, animal testing, clinical trials and reproductive rights,” the report reads.
Stating that the primary threat to the foundation’s agriculture program comes from its work promoting GMOs, the report notes the rise of anti-GMO campaigning in developing countries, including a “staunch opposition to GMOs in India.” It even names specific activists, such as the U.S.-based anti-GMO campaigner Jeffrey Smith.
The report also mentions the work of large organizations like Greenpeace and PETA as well as alternative media outlets like the Center for Public Integrity, Mother Jones, AlterNet and the LA Times, which had just published a seriesaccusing the foundation of “reap[ing] vast financial gains from investments in companies that contribute to the human suffering in health, housing and social welfare.”
Wikileaks published the threat assessment as part of its release of more than 5 million Stratfor emails in 2012.
4. Pharma intel and espionage operation
In 1996, Pfizer, one of the world’s largest pharmaceutical companies, conducted clinical trials in Nigeria for an antibiotic called Trovan. The results were devastating, as Nigerian officials reported more than 50 children died in the experiment and dozens became disabled.
In 2006, a Nigerian government panel concluded that Pfizer violated international law and called the experiment “an illegal trial of an unregistered drug.” In 2007, Nigerian state and federal authorities sued Pfizer for $7 billion, alleging the company did not have proper consent from the children’s parents.
A 2009 U.S. diplomatic cable published by Wikileaks revealed that while the case was in federal court, Pfizer had hired a private intelligence firm to get blackmail on Nigerian Attorney General Michael Aondoakaa.
According to the cable, “Pfizer’s investigators were passing this information to local media,” who published articles on the attorney general’s “alleged” corruption. “Aondoakaa’s cronies were pressuring him to drop the suit for fear of further negative articles,” it reads.
A few months after the negative articles, the Nigerian ministry of justice signed a settlement with Pfizer.
5. U.S. is a climate bully
Cables disclosed by Wikileaks in 2010 present the U.S. using what The Guardian called “spying, threats and promises of aid” to get international support for the 2009 Copenhagen Accord — an industry-friendly international climate deal with non-binding agreements to lower emissions. (Climate activist Naomi Klein described, at the time, the accord as “nothing more than a grubby pact between the world’s biggest emitters”.)
The State Department sent a secret cable to foreign embassies seeking human intelligence, or “dirt,” on UN diplomats regarding climate policy. And, as reported by Democracy Now!, the cables also indicated that the U.S. cut funding to Bolivia and Ecuador after both governments opposed the accord.
Bill McKibben, founder of the climate organization 350.org, said the cables exposed that “the U.S. was both bullying and buying countries into endorsing their do-little position on climate.”
6. International organizations consulting with Big Pharma
In 2009, Wikileaks revealed documents that the International Federation of Pharmaceutical Manufacturers & Associations (IFPMA) gave its members a report by the UN’s World Health Organization(WHO)’s Expert Working Group on research and development financing.
IFPMA members include pharmaceutical giants like Bayer, Johnson & Johnson, Merck, Novartis, Pfizer and Sanofi, and the organization represents these entities when dealing with the UN. What makes the Wikileaks document dump significant is that the working group gave IFPMA access to these documents months before their scheduled public release, suggesting that the UN’s health expert group was more accountable to the pharmaceutical industry than to its own member states.
“The compilation of documents shows the influence of ‘Big Pharma’ on the policy making decisions of the WHO,” Wikileaks commented when publishing the files.
“What’s in a name? That which we call a rose by any other name would smell as sweet.” ~ William Shakespeare
By Catherine Austin Fitts
I am not a scientist. I am not a doctor. I am not a biotech engineer. I am not an attorney. However, I read, listen, appreciate, and try to understand those who are.
I was an investment banker until politics made it impossible to continue to practice my art. I was trained as a portfolio strategist—so I map my world by watching the financial flows and allocation of resources. I was also trained as a conspiracy generator and foot soldier—conspiracies being the fundamental organizing principle of how things get done in our world. It was not until I left the establishment that I learned that those not in the club had been trained to disparage and avoid conspiracies—a clever trick that sabotages their efforts to gather power.
My response to living at war with agencies of the U.S. government for a time was to answer the questions of people who were sufficiently courageous and curious to solicit my opinion. Over many years, that response transformed into two businesses. One was The Solari Report, which continues to grow as a global intelligence network—we seek to help each other understand and navigate what is happening and contribute to positive outcomes. The other was serving as an investment advisor to individuals and families through Solari Investment Advisory Services. After ten years, I converted that business to doing an ESG screen. What those who use it want—that is not otherwise readily available in the retail market—is a screen that reflects knowledge of financial and political corruption. Tracking the metastasizing corruption is an art, not a science.
When you help a family with their finances, it is imperative to understand all their risk issues. Their financial success depends on successful mitigation of all the risks—whether financial or non-financial—that they encounter in their daily lives. Non-financial risks can have a major impact on the allocation of family resources, including attention, time, assets, and money.
Many of my clients and their children had been devastated and drained by health care failures and corruption—and the most common catalyst for this devastation was vaccine death and injury. After their lengthy and horrendous experiences with the health care establishment, they would invariably ask, “If the corruption is this bad in medicine, food, and health, what is going on in the financial world?” Chilled by the thought, they would search out a financial professional who was schooled in U.S. government and financial corruption. And they would find me.
The result of this flow of bright, educated people blessed with the resources to pay for my time was that, for ten years, I got quite an education about the disabilities and death inflicted on our children by what I now call “the great poisoning.” I had the opportunity to repeatedly price out the human damage to all concerned—not just the affected children but their parents, siblings, and future generations—mapping the financial costs of vaccine injury again and again and again. These cases were not as unusual as you might expect. Studies indicate that 54% of American children have one or more chronic diseases. Doctors who I trust tell me that number is actually much higher, as many children and their families cannot afford the care and testing necessary to properly diagnose what ails them.
One of the mothers featured in VAXXED—a must-watch documentary for any awake citizen, as is its sequel VAXXED II: The People’s Truth—estimated that a heavily autistic child would cost present value $5MM to raise and care for over a lifetime. When my clients who were grandparents insisted that they would not interfere with their children’s vaccine choices because it was “none of their business,” I would say, “Really? Who has the $5MM? You or your kids? When your kids need the $5MM to raise their vaccine-injured child, are you going to refuse them? You are the banker, and it is your money that is at risk here, so it is your business. Do you want to spend that $5MM on growing a strong family through the generations or on managing a disabled child who did not have to be disabled?” Often, that $5MM in expenditures also translates into divorce, depression, and lost opportunities for siblings.
My clients helped me find the best resources—books, documentaries, articles—on vaccines. You will find many of them linked or reviewed at The Solari Report, including in our Library.
Of all the questions that I had, the one that I spent the most time researching and thinking about was why. Why was the medical establishment intentionally poisoning generations of children? Many of the writers who researched and wrote about vaccine injury and death assumed it was an aberration—resulting from the orthodoxy of a medical establishment that could not face or deal with its mistakes and liabilities. That never made sense to me. Writings by Forrest Maready, Jon Rappoport, Dr. Suzanne Humphries and Arthur Firstenberg have helped me understand the role of vaccines in the con man trick of saving money for insurance companies and the legally liable.
Here is one example of how the trick may play out. A toxin creates a disease. The toxin might be pesticides or industrial pollution or wireless technology radiation. The toxin damages millions of people and their communities. Companies or their insurance provider may be liable for civil or criminal violations. Then a virus is blamed. A “cure” is found in a “vaccine.” The pesticide or other toxic exposure is halted just as the vaccine is introduced, and presto, the sickness goes away. The vaccine is declared a success, and the inventor is declared a hero. A potential financial catastrophe has been converted to a profit, including for investors and pension funds. As a portfolio strategist, I admit it has been a brilliant trick and likely has protected the insurance industry from the bankrupting losses it would experience if it had to fairly compensate the people and families destroyed.
Thanks to the work of Robert Kennedy and Mary Holland of Children’s Health Defense, I now understand the enormous profits generated by so-called “vaccines” subsequent to the passage of the National Childhood Vaccine Injury Act of 1986 and the creation of the National Vaccine Injury Compensation Program—a federal no-fault mechanism for compensating vaccine-related injuries or deaths by establishing a claim procedure involving the United States Court of Federal Claims and special masters. Call a drug or biotech cocktail a “vaccine,” and pharmaceutical and biotech companies are free from any liabilities—the taxpayer pays. Unfortunately, this system has become an open invitation to make billions from “injectibles,” particularly where government regulations and laws can be used to create a guaranteed market through mandates. As government agencies and legislators as well as the corporate media have developed various schemes to participate in the billions of profits, significant conflicts of interest have resulted.
The Public Readiness and Emergency Preparedness Act (PREPA or the PREP Act) became law in 2005, adding to corporate freedoms from liability. The Act “is a controversial tort liability shield intended to protect vaccine manufacturers from financial risk in the event of a declared public health emergency. The act specifically affords to drug makers immunity from potential financial liability for clinical trials of . . . vaccine at the discretion of the Executive branch of government. PREPA strengthens and consolidates the oversight of litigation against pharmaceutical companies under the purview of the secretary of Health and Human Services.” (~ Wikipedia)
Over time, this has evolved to the engineering of epidemics—the medical version of false flags. In theory, these can be “psyops” or events engineered with chemical warfare, biowarfare, or wireless technology. If this sounds strange, dive into all the writings of the “Targeted Individuals.”
I learned about this first-hand when I was litigating with the Department of Justice and was experiencing significant physical harassment. I tried to hire several security firms; they would check my references and then decline the work, saying it was too dangerous. The last one took pity and warned me not to worry about electronic weaponry, letting me know that my main problem would be low-grade biowarfare. This biowarfare expert predicted that the opposing team would drill holes in the wall of my house and inject the “invisible enemy.” Sure enough, that is exactly what happened. I sold my house and left town. That journey began a long process of learning how poisoning and nonlethal weapons are used—whether to move people out of rent-controlled apartments, sicken the elderly to move them to more expensive government-subsidized housing, gangstalk political or business targets, or weaken or kill litigants—and the list goes on. Poisoning turned out to be a much more common tactic in the game of political and economic warfare in America than I had previously understood.
After I finished my litigation, I spent several years detoxing from heavy metal toxicity—including from lead, arsenic, and aluminum. As I drove around America, I realized it was not just me. Americans increasingly looked like a people struggling with high loads of heavy metals toxicity. In the process of significantly decreasing my unusually high levels of heavy metals, I learned what a difference the toxic load had made to my outlook, my energy, and my ability to handle complex information.
This brings me to the question of what exactly a vaccine is and what exactly is in the concoctions being injected into people today as well as the witches’ brews currently under development.
In 2017, Italian researchers reviewed the ingredients of 44 types of so-called “vaccines.” They discovered heavy metal debris and biological contamination in every human vaccine they tested. The researchers stated, “The quantity of foreign bodies detected and, in some cases, their unusual chemical compositions baffled us.” They then drew the obvious conclusion, namely, that because the micro- and nanocontaminants were “neither biocompatible nor biodegradable,” they were “biopersistent” and could cause inflammatory effects right away—or later (http://medcraveonline.com/IJVV/IJVV-04-00072.pdf)
Whatever the ingredients of vaccines have been to date, nothing is more bizarre and unsettling than the proposals of what might be included in them in the future. Strategies—already well-funded and well on the way—include brain-machine interface nanotechnology, digital identity tracking devices, and technology with an expiration date that can be managed and turned off remotely. One report indicates that the Danish government and U.S. Navy had been paying a tech company in Denmark to make an injectible chip that would be compatible with one of the leading cryptocurrencies.
I was recently reading Mary Holland’s excellent 2012 review of U.S. vaccine court decisions (“Compulsory vaccination, the Constitution, and the hepatitis B mandate for infants and young children,” Yale Journal of Health Policy, Law, and Ethics) and I froze and thought, “Why are we calling the injectibles that Bill Gates and his colleagues are promoting ‘vaccines’? Are they really vaccines?”
Most people are familiar with how Bill Gates made and kept his fortune. He acquired an operating system that was loaded into your computer. It was widely rumored that the U.S. intelligence agencies had a back door. The simultaneous and sudden explosion of computer viruses then made it necessary to regularly update your operating system, allowing Gates and his associates to regularly add whatever they wanted into your software. One of my more knowledgeable software developers once said to me in the 1990s—when Microsoft really took off—”Microsoft makes really sh***y software.” But of course, the software was not really their business. Their business was accessing and aggregating all of your data. Surveillance capitalism was underway.
The Department of Justice launched an antitrust case against Microsoft in 1998, just as the $21 trillion started to disappear from the U.S. government—no doubt with the help of specially designed software and IT systems. During the settlement negotiations that permitted Gates to keep his fortune, he started the Gates Foundation and his new philanthropy career. I laughed the other day when my tweet of one of Robert Kennedy Jr.’s articles from Children’s Health Defense—describing the gruesome technology Gates is hoping to roll out through “injectibles”—inspired a response: “Well, I guess he is finally fulfilling his side of his antitrust settlement.”
If you look at what is being created and proposed in the way of injectibles, it looks to me like these technological developments are organized around several potential goals.
The first and most important goal is the replacement of the existing U.S. dollar currency system used by the general population with a digital transaction system that can be combined with digital identification and tracking. The goal is to end currencies as we know them and replace them with an embedded credit card system that can be integrated with various forms of control, potentially including mind control. “De-dollarization” is threatening the dollar global reserve system. The M1 and M2 money supply have increased in the double digits over the last year as a result of a new round of quantitative easing by the Fed. The reason we have not entered into hyperinflation is because of the dramatic drop in money velocity occasioned by converting Covid-19 into an engineered shutdown of significant economic activity and the bankrupting of millions of small and medium-sized businesses. The managers of the dollar system are under urgent pressure to use new technology to centralize economic flows and preserve their control of the financial system.
Just as Gates installed an operating system in our computers, now the vision is to install an operating system in our bodies and use “viruses” to mandate an initial installation followed by regular updates.
Now I appreciate why Gates and his colleagues want to call these technologies “vaccines.” If they can persuade the body politic that injectible credit cards or injectible surveillance trackers or injectable brain-machine interface nanotechnologies are “vaccines,” then they can enjoy the protection of a century or more of legal decisions and laws that support their efforts to mandate what they want to do. As well, they can insist that U.S. taxpayers fund, through the National Vaccine Injury Compensation Program, the damages for which they would otherwise be liable as a result of their experiments—and violations of the Nuremberg Code and numerous civil and criminal laws—on the general population. The scheme is quite clever. Get the general population to go along with defining their new injectible high-tech concoctions as “vaccines,” and they can slip them right into the vaccine pipeline. No need to worry about the disease and death that will result from something this unnatural delivered this quickly. The freedom from liability guaranteed by the PREP Act through the declaration of an emergency—and the ability to keep the emergency going through contact tracing—can protect them from liability for thousands if not millions of deaths and disabilities likely to follow such human experimentation. Ideally, they can just blame the deaths on a virus.
A colleague once told me how Webster’s Dictionary came about. Webster said that the way the evildoers would change the Constitution was not by amending it but by changing the definitions—a legal sneak attack.
I believe that Gates and the pharma and biotech industries are literally reaching to create a global control grid by installing digital interface components and hooking us up to Microsoft’s new $10 billion JEDI cloud at the Department of Defense as well as Amazon’s multibillion cloud contract for the CIA that is shared with all U.S. intelligence agencies. Why do you think President Trump has the military organizing to stockpile syringes for vaccines? It is likely because the military is installing the roaming operating system for integration into their cloud. Remember—the winner in the AI superpower race is the AI system with access to the most data. Accessing your body and my body on a 24/7 basis generates a lot of data. If the Chinese do it, the Americans will want to do it, too. In fact, the rollout of human “operating systems” may be one of the reasons why the competition around Huawei and 5G telecommunications has become so fractious. As Frank Clegg, former President of Microsoft Canada has warned us, 5G was developed by the Israelis for crowd control.
In the face of global “de-dollarization,” this is how the dollar syndicate can assert the central control it needs to maintain and extend its global reserve currency financial power. This includes protecting its leadership from the civil and criminal liability related to explosive levels of financial and health care fraud in recent decades.
Which brings me back to you and me. Why are we calling these formulations “vaccines”? If I understand the history of case law, vaccines, in legal terms, are medicine. Intentional heavy metal poisoning is not medicine. Injectible surveillance components are not medicine. Injectible credit cards are not medicine. An injectible brain-machine interface is not a medicine. Legal and financial immunity for insurance companies does not create human immunity from disease.
We need to stop allowing these concoctions to be referred to by a word that the courts and the general population define and treat as medicine and protect from legal and financial liability.
The perpetrators of this fraud are trying a very neat trick—one that will help them go much faster and cancel out a lot of risk—at our expense. I understand why they are doing it.
What I don’t understand is why we are helping them. Why are we acquiescing in calling these bizarre and deeply dangerous concoctions “vaccines”? Whatever they are, they are not medicine.
So, what shall our naming convention be? What name shall we give to the relevant poisons, neurologically damaging metals, and digital shackles?
Whatever we call them, I know one thing. THEY ARE NOT MEDICINE, WHICH MEANS THEY SURE ARE NOT VACCINES.
On Friday, July 31, in a column ostensibly dealing with health care “misinformation,” Washington Post media critic Margaret Sullivan opened by lambasting “fringe doctors spouting dangerous falsehoods about hydroxychloroquine as a COVID-19 wonder cure.”
Actually, it was Sullivan who was spouting dangerous falsehoods about this drug, something the Washington Post and much of the rest of the media have been doing for months. On May 15, the Post offered a stark warning to any Americans who may have taken hope in a possible therapy for COVID-19. In the newspaper’s telling, there was nothing unambiguous about the science — or the politics — of hydroxychloroquine: “Drug promoted by Trump as coronavirus game-changer increasingly linked to deaths,” blared the headline. Written by three Post staff writers, the story asserted that the effectiveness of hydroxychloroquine in treating COVID-19 is scant and that the drug is inherently unsafe.
This claim is nonsense
Biased against the use of hydroxychloroquine for COVID-19 — and the Washington Post is hardly alone — the paper described an April 21, 2020, drug study on U.S. Veterans Affairs patients hospitalized with the illness. It found a high death rate in patients taking the drug hydroxychloroquine. But this was a flawed study with a small sample, the main flaw being that the drug was given to the sickest patients who were already dying because of their age and severe pre-existing conditions. This study was quickly debunked. It had been posted on a non-peer-reviewed medical archive that specifically warns that studies posted on its website should not be reported in the media as established information.
Yet, the Post and countless other news outlets did just the opposite, making repeated claims that hydroxychloroquine was ineffective and caused serious cardiac problems. Nowhere was there any mention of the fact that COVID-19 damages the heart during infection, sometimes causing irregular and sometimes fatal heart rhythms in patients not taking the drug.
To a media unrelentingly hostile to Donald Trump, this meant that the president could be portrayed as recklessly promoting the use of a “dangerous” drug. Ignoring the refutation of the VA study in its May 15 article, the Washington Post cited a Brazil study published on April 24 in which a COVID trial using chloroquine (a related but different drug than hydroxychloroquine) was stopped because 11 patients treated with it died. The reporters never mentioned another problem with that study: The Brazilian doctors were giving their patients lethal cumulative doses of the drug.
On and on it has gone since then, in a circle of self-reinforcing commentary. Following the news that Trump was taking the drug himself, opinion hosts on cable news channels launched continual attacks on both hydroxychloroquine and the president. “This will kill you!” Fox News Channel’s Neil Cavuto exclaimed. “The president of the United States just acknowledge that he is taking hydroxychloroquine, a drug that [was] meant really to treat malaria and lupus.”
Washington Post reporters Ariana Cha and Laurie McGinley were back again on May 22, with a new article shouting out the new supposed news: “Antimalarial drug touted by President Trump is linked to increased risk of death in coronavirus patients, study says.” The media uproar this time was based on a large study just published in the Lancet. There was just one problem. The Lancet paper was fraudulent and it was quickly retracted.
However, the damage from the biased media storm was done and it was long-lasting. Continuing patient enrollment needed for early-use clinical trials of hydroxychloroquine dried up within a week. Patients were afraid to take the drug, doctors became afraid to prescribe it, pharmacies refused to fill prescriptions, and in a rush of incompetent analysis and non-existent senior leadership, the FDA revoked its Emergency Use Authorization for the drug.
So what is the real story on hydroxychloroquine? Here, briefly, is what we know:
When the COVID-19 pandemic began, a search was made for suitable antiviral therapies to use as treatment until a vaccine could be produced. One drug, hydroxychloroquine, was found to be the most effective and safe for use against the virus. Federal funds were used for clinical trials of it, but there was no guidance from Dr. Anthony Fauci or the NIH Treatment Guidelines Panel on what role the drug would play in the national pandemic response. Fauci seemed to be unaware that there actually was a national pandemic plan for respiratory viruses.
Following a careful regimen developed by doctors in France, some knowledgeable practicing U.S. physicians began prescribing hydroxychloroquine to patients still in the earlyphase of COVID infection. Its effects seemed dramatic. Patients still became sick, but for the most part they avoided hospitalization. In contrast — and in error — the NIH-funded studies somehow became focused on giving hydroxychloroquine to late-presenting hospitalized patients. This was in spite of the fact that unlike the drug’s early use in ambulatory patients, there was no real data to support the drug’s use in more severe hospitalized patients.
By April, it was clear that roughly seven days from the time of the first onset of symptoms, a COVID-19 infection could sometimes progress into a more radical late phase of severe disease with inflammation of the blood vessels in the body and immune system over-reactions. Many patients developed blood clots in their lungs and needed mechanical ventilation. Some needed kidney dialysis. In light of this pathological carnage, no antiviral drug could be expected to show much of an effect during this severe second stage of COVID.
On April 6, 2020, an international team of medical experts published an extensive study of hydroxychloroquine in more than 130,000 patients with connective tissue disorders. They reaffirmed that hydroxychloroquine was a safe drug with no serious side effects. The drug could safely be given to pregnant women and breast-feeding mothers. Consequently, countries such as China, Turkey, South Korea, India, Morocco, Algeria, and others began to use hydroxychloroquine widely and early in their national pandemic response. Doctors overseas were safely prescribing the drug based on clinical signs and symptoms because widespread testing was not available.
However, the NIH promoted a much different strategy for the United States. The “Fauci Strategy” was to keep early infected patients quarantined at home without treatment until they developed a shortness of breath and had to be admitted to a hospital. Then they would they be given hydroxychloroquine. The Food and Drug Administration cluelessly agreed to this doctrine and it stated in its hydroxychloroquine Emergency Use Authorization (EUA) that “hospitalized patients were likely to have a greater prospect of benefit (compared to ambulatory patients with mild illness).”
In reality just the opposite was true. This was a tragic mistake by Fauci and FDA Commissioner Dr. Stephen Hahn and it was a mistake that would cost the lives of thousands of Americans in the days to come.
At the same time, accumulating data showed remarkable results if hydroxychloroquine were given to patients early, during a seven-day window from the time of first symptom onset. If given during this window, most infections did not progress into the severe, lethal second stage of the disease. Patients still got sick, but they avoided hospitalization or the later transfer to an intensive care unit. In mid-April a high-level memo was sent to the FDA alerting them to the fact that the best use for hydroxychloroquine was for its early use in still ambulatory COVID patients. These patients were quarantined at home but were not short of breath and did not yet require supplemental oxygen and hospitalization.
Failing to understand that COVID-19 could be a two-stage disease process, the FDA ignored the memo and, as previously mentioned, it withdrew its EUA for hydroxychloroquine based on flawed studies and clinical trials that were applicable only to late-stage COVID patients.
By now, however, some countries had already implemented early, aggressive, outpatient community treatment with hydroxychloroquine and within weeks were able to minimize their COVID deaths and bring their national pandemic under some degree of control.
In countries such as Great Britain and the United States, where the “Fauci-Hahn Strategy” was followed, there was a much higher death rate and an ever-increasing number of cases. COVID patients in the U.S. would continue to be quarantined at home and left untreated until they developed shortness of breath. Then they would be admitted to the hospital and given hydroxychloroquine outside the narrow window for the drug’s maximum effectiveness.
In further contrast, countries that started out with the “Fauci-Hahn Doctrine” and then later shifted their policy towards aggressive outpatient hydroxychloroquine use, after a brief lag period also saw a stunning rapid reduction in COVID mortality and hospital admissions.
Finally, several nations that had started using an aggressive early-use outpatient policy for hydroxychloroquine, including France and Switzerland, stopped this practice when the WHO temporarily withdrew its support for the drug. Five days after the publication of the fake Lancet study and the resulting media onslaught, Swiss politicians banned hydroxychloroquine use in the country from May27 until June 11, when it was quickly reinstated.
The consequences of suddenly stopping hydroxychloroquine can be seen by examining a graph of the Case Fatality Ratio Index (nrCFR) for Switzerland. This is derived by dividing the number of daily new COVID fatalities by the new cases resolved over a period with a seven-day moving average. Looking at the evolution curve of the CFR it can be seen that during the weeks preceding the ban on hydroxychloroquine, the nrCFR index fluctuated between 3% and 5%.
Following a lag of 13 days after stopping outpatient hydroxychloroquine use, the country’s COVID-19 deaths increased four-fold and the nrCFR index stayed elevated at the highest level it had been since early in the COVID pandemic, oscillating at over 10%-15%. Early outpatient hydroxychloroquine was restarted June 11 but the four-fold “wave of excess lethality” lasted until June 22, after which the nrCFR rapidly returned to its background value.
Here in our country, Fauci continued to ignore the ever accumulating and remarkable early-use data on hydroxychloroquine and he became focused on a new antiviral compound named remdesivir. This was an experimental drug that had to be given intravenously every day for five days. It was never suitable for major widespread outpatient or at-home use as part of a national pandemic plan. We now know now that remdesivir has no effect on overall COVID patient mortality and it costs thousands of dollars per patient.
Hydroxychloroquine, by contrast, costs 60 cents a tablet, it can be taken at home, it fits in with the national pandemic plan for respiratory viruses, and a course of therapy simply requires swallowing three tablets in the first 24 hours followed by one tablet every 12 hours for five days.
There are now 53 studies that show positive results of hydroxychloroquine in COVID infections. There are 14 global studies that show neutral or negative results — and 10 of them were of patients in very late stages of COVID-19, where no antiviral drug can be expected to have much effect. Of the remaining four studies, two come from the same University of Minnesota author. The other two are from the faulty Brazil paper, which should be retracted, and the fake Lancet paper, which was.
Millions of people are taking or have taken hydroxychloroquine in nations that have managed to get their national pandemic under some degree of control. Two recent, large, early-use clinical trials have been conducted by the Henry Ford Health System and at Mount Sinai showing a 51% and 47% lower mortality, respectively, in hospitalized patients given hydroxychloroquine. A recent study from Spain published on July 29, two days before Margaret Sullivan’s strafing of “fringe doctors,” shows a 66% reduction in COVID mortality in patients taking hydroxychloroquine. No serious side effects were reported in these studies and no epidemic of heartbeat abnormalities.
This is ground-shaking news. Why is it not being widely reported? Why is the American media trying to run the U.S. pandemic response with its own misinformation?
Steven Hatfill is a veteran virologist who helped establish the Rapid Hemorrhagic Fever Response Teams for the National Medical Disaster Unit in Kenya, Africa. He is an adjunct assistant professor in two departments at the George Washington University Medical Center where he teaches mass casualty medicine. He is principle author of the prophetic book “Three Seconds Until Midnight — Preparing for the Next Pandemic,” published by Amazon in 2019.
ER Editor: Of course, these claims cannot be verified given the anonymous nature of the source. Yet, it all has a ring of truth. Trump’s revealed he’s using hydroxychloroquine prophylactically (kudos – was he dropping us a hint?), so why would doctors, such as those hired for an American president no less, not be giving the same advice to other notables? Anything else makes little sense.
Note how this person calls COVID-19 a ‘bioweapon’ in ‘unrelenting launches of the COVID-19 bioweapon’ and ‘coronavirus cluster explosions will be detonated’. We only hope that herd immunity may short-circuit his/her predictions. The hypothesis that ‘Covid-19’ is in fact a bioweapon is something we’ve published on at length.
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Anonymous D.C. Insider Exposes Ultra-Secret Covid Conspiracy Inside the Beltway
STATE OF THE NATION
Submitted by an Anonymous D.C. Insider
Big Pharma and the WHO have known all along about the HCQ cure for COVID-19.
Everyone at the CDC, NIH and FDA knows that hydroxychloroquine (HCQ) is the silver bullet for the coronavirus.
They also know that, when combined with azithromycin and zinc, the 3-in-1 protocol provides the magic formula for almost anyone with coronavirus disease.
However, what Dr. Fauci, Dr. Birx and Robert Redfield are not telling anyone is that practically every VIP in Washington, D.C. is using HCQ prophylactically.
Everyone knows that Trump has been using it as a preventative as he publicly stated so on multiple occasions. But no one has revealed that virtually everyone inside the Beltway is also using it. That’s why they were all shown so often in groups with no masks and not adhering to the recommended social distancing guidelines during the regular coronavirus briefings. And, they did many of those dog and pony shows right in the middle of the Covid spikes during the first wave.
The real scandal here is that leading politicians, government officials, corporate CEOs and UN administrators all know about the efficacy of HCQ, and yet they have collaborated to deprive the American people of its use. All the while they, themselves, are secretly taking HCQ prophylactically.
When so many countries around the globe have used Hydroxychloroquine with great success, why is the U.S. fiercely resisting it?
Because the world’s most zealous vaccine salesman — Bill Gates — is determined to bring a COVID-19 vaccine to market. Word on the street (K Street) is that Gates is also taking HCQ as a preventive.In fact, he has taken HCQ as a precautionary measure to avoid malaria for many years during his travels to the Third World nations that were subjected to his endless vaccine pitches and vaccination programs.
If Americans knew that India was successfully using HCQ nationwide, how would they react? New Delhi has even made the decision to make HCQ available as a prophylactic, so inexpensive is it.
“India is estimated to produce 70% of the world’s hydroxychloroquine, with Ipca Labs and Zydus Cadila the two largest producers of the drug in the country.[1]
Key government officials, medical authorities and elected representatives throughout the USA are aware of every single fact stated in this exposé. Nevertheless, they are pushing untested remedies and dangerous protocols that have actually killed many COVID-19 patients in all 50 states.
This situation is completely unacceptable. Especially when the leaders of the national coronavirus response are taking HCQ and other effective prophylactics to keep the coronavirus at bay. The same goes for many in the mainstream media; they will never tell anyone either that they’re taking HCQ. Nor will the Sultans of Silicon Valley or Wall Street banksters or Corporate America moguls ever let on to this “ultra-secret conspiracy”. Which is why the Hamptons Concert With Goldman CEO, ‘Chainsmokers’ Faces N.Y. Probe. Goldman Sachs Chairman of the Board David Solomon obviously felt immune to catching Covid even at a concert where he was the star of the show.
But what’s the real scandal here?
The HCQ-Azithromycin-Zinc protocol is being deliberately withheld from the American people so that a mandatory COVID-19 vaccine can be foisted on the country.
And, the proof of such a criminal conspiratorial plot: there will be never-ending seasonal Covid spikes, with each wave being bigger and more intense than the previous one. When those start to ebb, coronavirus cluster explosions will be detonated in the major metro areas, particularly the sanctuary cities.
Then, when the blue states have had enough, the Democrat governors will collude with their Democrat legislatures to mandate an annual Covid vaccination (just like California recently passed draconian legislation requiring yearly compliance with childhood vaccination schedules). The unrelenting launches of the COVID-19 bioweapon in conservative territory will eventually compel the Republican governors to do the same in the red states.
— An Anonymous D.C. Insider
SOTN Editor’s Note: The end result of this phase of OPERATION COVID-19 is the undeclared state of medical martial law. Next will begin the initial stages of the Orwellian takeover scheme COVID-1984, which has been greatly advanced via the staged race riots and growing buzz about an impending race war. However, only if the American people allow them to will these treasonous plans gain any meaningful traction.
“We are talking about private contracts outside the scope of government. We’re talking about local barter, and the issuing of local currencies, the building of private money systems. During the Great Depression, many citizens looked around and said, ‘We still have land and food, we still have commodities. Nothing has changed here. We just have to invent a way to conduct commerce among ourselves.’ One estimate states that, during the Depression of the 1930s, there were 1500 private money systems across America.” (My notes for “The Underground”)
I have made my case concerning the fake pandemic. Many times now.
From the beginning—the failure to isolate, purify, or actually discover a novel coronavirus by correct procedures. The meaningless diagnostic tests and the meaningless case numbers. The propaganda. The use of “the virus” as a cover story obscuring high-level corporate and government crimes.
Of course, many people believe in the COVID-19 virus. And of these, some have been seeking treatments outside the bounds of government certification.
This is their right. They are exercising freedom in managing their own health. And so some of them are taking hydroxychloroquine (HCQ).
The FDA, which certifies all medical drugs as safe and effective, before they are released for public use, has not recommended HCQ for COVID treatment. It has banned the drug for that purpose, outside of hospitals and clinical trials.
The FDA‘s track record—which I’ve been documenting for the past 25 years—is a horror show. The first key review I became aware of was authored in 2000, by Dr. Barbara Starfield, and published on July 26th of that year, in the Journal of the American Medical Association. Starfield stated that, annually, FDA-approved medicines kill 106,000 Americans. That’s over a million Americans per decade. So relying on the FDA to decide whether HCQ is a useful drug is not a concession some Americans are willing to make.
Pharma and all its allies and minions and whores are focusing on a jackpot bonanza for COVID treatment: vaccines and new antiviral drugs. Pharma does not want competition. It definitely does not want to see a landscape in which all sorts of alternative treatments for COVID (or any purported disease) are rampant and free-wheeling.
We are seeing multiple censorship actions across platforms, when people, including doctors, speak positively about HCQ.
Fauci is very much in the pro-Pharma camp, of course. He and Gates want an RNA vaccine to come to market, by any means necessary. They also want antiviral drugs to dominate COVID treatment.
A very sharp reader spelled out the Pharma-anticipated future for these new (toxic) antiviral medicines. And not just for COVID. Up to now, there has been very little mainstream progress in getting drugs specifically designed to treat viruses into the marketplace. This is Pharma’s big opportunity. They envision a trillion-dollar operation that will elevate antivirals (for treating any viruses) to the level of, say, antibiotics, which are used against bacteria. COVID would simply be the first major “breakthrough.”
So we have a war going on. HCQ and other alternative modalities vs. vaccines and antivirals. Pharma does not want to lose this one. It would be disastrous.
I am not touting HCQ. I am putting it this way: if many people are convinced, or become convinced, that HCQ is a drug of choice, and if they believe it is helping them, then a major rebellion against Pharma and the FDA and its counterparts around the world takes off. It soars. And it spurs the use of other alternatives on which Pharma makes zero profits.
So-called natural health and alternative medicine have been booming since the 1980s. A new escalation would send very serious shock waves through the pharmaceutical industry.
Fauci is well aware of this. He is fronting for the industry in every possible way. Trump, with his statements favoring HCQ, has become a major threat in that regard.
When you see new reports of soaring COVID case numbers—a con which I’ve documented six ways from Sunday—you’re not only witnessing a planned strategy to maintain the war against the economy and therefore against billions of people whose lives are at stake; you’re also watching a justification for pushing antivirals and vaccines. For the benefit of Pharma.
The last thing the pharmaceutical industry wants to see is their own case-number con giving birth to wildcat outbreaks of health freedom. People leaving the nest. People going elsewhere for treatment.
Individuals making decisions about their own treatments—this is very serious business. People should look deeply before making choices. In the case of various HCQ protocols, they should consider: dosage levels; when in the course of illness the drug would be given (early or late); whether there is illness requiring treatment to begin with; whether people may have a heredity condition which could make HCQ perilous or even lethal—these are some of the relevant considerations.
The FDA and Pharma want to be the first and last word.
Life and Liberty say they are not the first and last word.
In that regard, there is another issue: licenses vs. contracts. The medical cartel, backed by governments, has established medical boards which grant licenses to practice medicine. These special persons, doctors, are handed the right to treat and cure diseases. This is an attempt to create a monopoly.
There is another avenue: private contracts. Here is the analogy I’ve used to describe this situation. Two adults, Joe and Fred, enter into an agreement. Joe says he has a health condition. He will be the patient. Fred will be the practitioner. Fred has a well on his property. Fred believes the water has a special healing quality. He will give some of it (or sell it) to Joe, who will drink it over the course of two weeks.
Both men, in their contract, agree that no legal liability will be attached to the outcome. They are both responsible. They are of sound mind. They don’t require government permission to sign or fulfill their contract.
That’s it in a nutshell.
Joe and Fred are operating on their own. They have that natural right. They also have the right to be wrong—in case the water treatment doesn’t work, or is harmful.
Of course, all sorts of meddlers will claim this arrangement is illegal and absurd. Meddlers always try to curb freedom. That’s their crusade in life. They can’t stand the idea of people making their own choices and decisions and then accepting the consequences.
I’m not saying governments will honor such contracts. Governments are prime meddlers. I’m saying these contracts (and not just in the arena of healing) stand outside governments. They are citizen-to-citizen. They are prior to government. They are intrinsically more real than government.
CENSORSHIP: CDC Takes Over Frontline Doctors’ Website and Replaces Content with Their Own Data
After the Frontline Doctors website was removed, someone bought the domain name with a .org ending and redirected it to the CDC website on COVID-19. This screenshot shows what appears when you type americasfrontlinedoctors.org into your browser.
by Brian Shilhavy Editor, Health Impact News
As we have been reporting this week, a group of doctors who have been on the front lines treating COVID patients, successfully, descended upon Washington D.C. this week to conduct press conferences and a 2-day “White Coat Summit” to share their experiences in treating, and curing, their COVID patients.
They claim that they represent “thousands” of doctors who have been censored.
Their first press conference was sparsely attended by the Washington D.C. media, and the only media company that filmed it and shared it online, Breitbart News, was immediately censored, and the video was quickly deleted from Facebook, YouTube, and Twitter.
But the video of that press conference has been preserved, and has now been viewed by over 20 million people, and our own copy that we have published on our Bitchute Channel has been viewed over 125,000 times so far.
The Frontline Doctor’s Website was removed from the Internet. This was the page advertising their White Coat Summit in Washington D.C. earlier this week. It has been replaced with the CDC Website page on the Coronavirus.
The next day, the Frontline Doctors’ website, which used to be at https://www.americasfrontlinedoctors.com, was removed by the company that was hosting it.
WOW: Our website host @Squarespace has just completely and arbitrarily shut down our website, claiming a violation of their terms of service.
We are a group of physicians advocating for a better understanding of COVID-19 and its available treatment options.
Two days ago, the same day as the first press conference, someone bought the domain americasfrontlinedoctors.org, which now displays the CDC’s official website about COVID-19. (See image at the top of this article.)
Why is this Life-Saving Information being Censored?
The reason why the U.S. Government and their “health” agencies, as well as Big Tech, are censoring this information is very simple: cures to diseases are not profitable.
Millions of Americans are out of work, tens of thousands of small businesses have closed, and the largest transfer of wealth in the history of the United States has occurred during the past few months, allocating close to 2 TRILLION dollars to Big Pharma, most of it for COVID vaccines.
And all of this is a CRIMINAL ACT against the American people, if what these Frontline Doctors say is true, which is that there is a simple cure for COVID, and that “nobody has to die” from it.
When you understand what is truly happening in America and around the world today, then it is very easy to understand why Big Pharma, Big Tech, and the U.S. Government, all of whom will profit from COVID vaccines and interventions, while at the same time putting into place massive surveillance systems to take away our freedoms, would want to silence this group of doctors who simply want to stop their patients from dying due to the COVID fear.
Here is the full Summit from Day 1 which is also hard to find.
Here is the Day 2 Session:
Here is the list of Speakers that was originally published on their website that is now gone:
Speakers
Dr. Jeffrey Barke
Schools Liaison
Dr. Jeffrey Barke is a Board Certified primary care physician in private practice for over 25 years. He completed his medical school and family practice residency at the University of California, Irvine. He has served as an Associate Clinical Professor at U.C. Irvine and a board member of the Orange County Medical Association. He is also a reserve deputy and a tactical physician for a local law enforcement SWAT team. Dr. Barke served as an elected school board member for the Los Alamitos Unified School District for 12 years and is the cofounder and current school board Chair of the free public charter school Orange County Classical Academy. Dr. Barke is married to his high school sweetheart and has two adult children.
Dr. Scott Barbour
Business Liason
Dr. Scott Barbour is the founder and owner of Barbour Orthopaedics & Spine with five clinics and a surgery center in Atlanta, Georgia. Dr. Barbour is fellowship-trained in sports medicine (Palo Alto medical foundation). Dr. Barbour has been a team physician for several professional sports teams including the Oakland Raiders, San Jose Sharks, USA Rugby Teams. He is currently the team physician for the Atlanta franchise of Major League Rugby professional rugby team. Dr. Barbour has appeared on numerous radio and television shows. He has published articles and book chapters on Orthopedic surgery and has been an editor for American Journal of Sports Medicine. He currently co-hosts “The Doctors Lounge” podcast on America’s Web Radio and is a board member of Docs4PatientCare foundation.
Simone Gold, MD, JD, FABEM
Founder
Dr. Simone Gold, MD, JD, FABEM, is a board certified emergency physician. She graduated from Chicago Medical School before attending Stanford University Law School to earn her Juris Doctorate degree. She completed her residency in Emergency Medicine at Stony Brook University Hospital in New York. Dr. Gold worked in Washington D.C. for the Surgeon General, as well as for the Chairman of the Labor & Human Resources Committee. She works as an emergency physician on the front-lines whether or not there is a pandemic. Her clinical work serves all Americans: from urban-inner city, to suburban and the Native American population. Her legal work focuses on policy issues relating to law and medicine.
Dr. Teryn Clarke. MD
Communications Director
Dr. Clarke is a board-certified neurologist. Her focus is on the diagnosis and management of Alzheimer’s Disease and other cognitive disorders. Her mission to educate the community and optimize lifestyle for brain health and general health. The Alzheimer’s Foundation of America selected her as their Dementia Care Professional of the Year in 2015. During the pandemic, she has remained focused on the health and psychological needs of seniors. She is now working within her community to identify and treat deficiencies to boost immune system function in this vulnerable population.
Dr. Robert Hamilton
Schools Liason
Dr. Robert C. Hamilton, M.D. has been a general pediatrician in Santa Monica, CA for 36 years. He studied medicine at UCLA Medical School and did his pediatric residency and Chief Residency at UCLA Medical Center as well. He is a former President of the Los Angeles Pediatric Society. Dr. Hamilton founded ‘Lighthouse Medical Missions’, a volunteer organization that organizes short-term medical missions to Africa, Asia, Central and South America. He has travelled to Africa on medical teams 26 times and his most recent trip was to Colombia to aid Venezuelan refugees leaving their country.
He is also the creator of the ‘Hamilton Hold’, a technique for calming crying babies that has been seen by over 44 million viewers worldwide on YouTube. In 2018 he authored 7 Secrets of the Newborn. He has written editorial articles for the Wall Street Journal, and appeared as a television guest on Good Morning America, The Doctor Oz Show, Fox’s Morning Show, Beijing’s CCTV show ‘Challenge Impossible’ and on Fox’ The Ingraham Angle. He has also been a guest on the Dennis Prager radio show and Eric Metaxis’ podcast. Finally, he is the host of his own podcast entitled, ‘The Hamilton Review: Where Kids and Culture Collide’.
Dr. Hamilton is the father of 6 children and the grandfather of 9 grandchildren.
Dr. Kristin Held
Policy Liaison
Dr. Kirstin Held is a board-certified ophthalmologist and ophthalmic surgeon. She is a Phi Beta Kappa Graduate from the University of Texas at Austin and received her medical degree from the University of Texas Medical School at San Antonio, where she was elected to AOA. In 2018, she received the Lifetime Achievement Award from the National Association of Women Business Owners in San Antonio. She served on the healthcare advisory team for Dr. Ben Carson during his presidential campaign and is Co-Chair of the Healthcare Advisory Council for Congressman Chip Roy. Dr. Held has had numerous articles published, including in the Washington Times, Houston Chronicle, The Hill, Journal of American Physicians and Surgeons and Dr. Carson’s American Currentsee. She has spoken across the country advocating for the patient-physician relationship and she actively shares healthcare policy information with over 48K followers on Twitter.
Dr. Held is married and has four daughters; two are physicians, and two are in business. She is proud to be an 8 year cancer survivor and remains forever grateful to her brilliant physicians and surgeons.
Dr. Mark McDonald
Mental Health Liason
Dr. McDonald trained in both adult and child & adolescent psychiatry at UCLA and achieved double board certification. For the past eight years, he has also trained in adult psychoanalysis. He now specializes in child and adolescent psychiatry. Dr. McDonald has lived and worked in Europe, Asia, and Central America, and he is proficient in Japanese, Spanish, and French. He studied classical music, history, and literature at UC Berkeley. Before beginning his medical education, he taught in public schools. His opinions on the need to re-open America’s schools have been widely published in local and national news, including the Wall Street Journal and The Federalist.
Dr. Joseph A. Ladapo
Policy Liason
Dr. Ladapo, MD, PhD, is a physician and health policy researcher whose primary interests include health economics, technology evaluation, and interventions to reduce cardiovascular disease risk. He is Associate Professor-in-Residence at the David Geffen School of Medicine at UCLA. His research program is funded by the National Institutes of Health, and his writings have appeared in the Washington Post, USA Today, and the Wall Street Journal. Dr. Ladapo graduated from Wake Forest University and received his MD from Harvard Medical School and his PhD in Health Policy from Harvard Graduate School of Arts and Sciences.<
Dr. James Todaro, MD
Investigative Liason<
Dr. James Todaro received his medical degree from Columbia University College of Physicians and Surgeons in New York. He then completed his ophthalmology residency. He continues to lead investigative research in COVID-19 on a global scale. He wrote the first widely read paper on chloroquine in treatment of COVID-19 in An Effective Treatment for Coronavirus (COVID-19), and most recently the first detailed exposé on Surgisphere in A Study Out of Thin Air. His early discovery of the fraudulent data investigation led to what is now referred to as #LancetGate – the stunning once-in-a-generation retraction of the now infamous The Lancet study that had led to the European Union and the WHO halting studies of HCQ.
Dr. Richard Urso
Science Liaison
This is MURDER – Crimes Against Humanity
Let’s start calling this what it really is. This is MASS MURDER, with crimes against humanity being committed which should be prosecuted as TREASON.
And things are only going to get worse, if the American public continues to obey everything they are being told to do and just willingly surrender their freedoms and former way of life.
Because the vaccines are coming next, and they are being fast-tracked without proper testing, for a virus which has never even been isolated in a laboratory, and for which no accurate test exists because the 100+ tests currently in the market have all been fast-tracked as well, and are highly inaccurate. See:
(UPDATE: Earlier today – July 29, 2020 – we published this interview between Del Bigtree and Dr. Andrew Kaufman which had been on the Highwire YouTube channel since July 16th, and had well over 100K views. About an hour after we published this article, it disappeared. So here is a copy from our Bitchute channel.)
