A Little (Snake) Oil With that Pill

(NOTE:  Also check out James Corbett’s Series on  Rockefeller Medicine:   https://www.corbettreport.com/rockefeller-medicine-video/)

Western Medicine is Rockefeller Medicine – All The Way

Published 7 years ago on

AT A GLANCE…

  • THE STORY:How did Western Medicine, also known as Allopathy, originate? How did it overtake others systems of healing & medicine? How are the Rockefellers, oil barons & NWO banking family, involved?
  • THE IMPLICATIONS:What is the point of just taking drugs to mask symptoms when they don’t actually cure you? How much can Western medicine truly heal you when it is so tightly controlled by Big Pharma? Are synthetic petrochemical drugs a kind of poison, in and of themselves?
western-medicine

How many must feel, stuck on the Western medicine hamster wheel of pill after pill after pill …

Loading…Western medicine is Rockefeller

Western medicine has some good points, for sure, and is great in an emergency, but it’s high time people realized that today’s mainstream medicine (western medicine or allopathy), with its focus on drugs, radiation and surgery, is at its foundation a Rockefeller creation. The Rockefellers, of course, are one of the most rich and powerful families of the NWO (New World Order) black nobility. Behind their spurious facade of philanthropy, they are power-hungry tyrants intent on owning the entire world, and depopulating it through eugenics-based programs like forced sterilization, water fluoridation, abortions and vaccinations. They have either majorly or fully created (and still dominate) the United Nations, the World Health Organization, the Council on Foreign Relations, the Trilateral Commission, Planned Parenthood and many, many other organizations that either rule the world or influence culture to a large extent.

Despite the dominance of western medicine nowadays, even just 100 years ago the situation was very different, so it’s worthwhile casting our minds back to how the we got to this place. How did western medicine and the giant conglomerate of multinational pharmaceutical corporations (“Big Pharma”) become the mainstream medical system in the US and other first world nations? And what alternatives are there?

Petroleum Drugs

Let’s go back in time to the late 1800s. John D. Rockefeller, a man quoted to have said “competition is sin”, is the head of the Rockefeller family and has just become very rich through extracting oil from the ground. Now he is looking for ways to capitalize even further with his oil, and he comes across the idea of using coal tar – a petroleum derivative – to make substances that affect the human mind, body and nervous system. These are called drugs, and they are excellent at masking or stopping symptoms, but overall do not cure the underlying cause of a disease.

Like other elite leaders of the New World Order who fit the description of an “evil genius” – those high on intellect and low on compassion – Rockefeller used his oil money to buy out part of the massive German pharmaceutical cartel, I.G. Farben. This was the very same cartel that would later assist Hitler to implement his eugenics-based vision of a New World Order founded on racial supremacy, by manufacturing chemicals and poisons for war. With the control of drug manufacturing under his wings, Rockefeller then embarked on a decidedly wicked plan – wicked from the point of view of a free and healthy humanity, but brilliant from a business perspective.

western-medicine-rockefeller-medicine-petroleum-drugs

Western medicine relies on Big Pharma’s petroleum drugs, which the body can never ultimately assimilate. Meanwhile, it engages in biopiracy to steal Nature’s best compounds and patent them.

Destroying any Competition to Western Medicine

Rockefeller saw that there were many types of doctors and healing modalities in existence at that time, from chiropractic to naturopathy to homeopathy to holistic medicine to herbal medicine and more. He wanted to eliminate the competitors of western medicine (the only modality which would propose drugs and radiation as treatment, thus enriching Rockefeller who owned the means to produce these treatments), so he hired a man called Abraham Flexner to submit a report to Congress in 1910. This report “concluded” that there were too many doctors and medical schools in America, and that all the natural healing modalities which had existed for hundreds or thousands of years were unscientific quackery. It called for the standardization of medical education, whereby only the allopathic-based AMA be allowed to grant medical school licenses in the US.

Sadly, Congress acted upon the conclusions and made them law. Incredibly, allopathy became the standard mainstream modality, even though its 3 main methods of treatment in the 1800s had been blood-letting, surgery and the injection of toxic heavy metals like lead and mercury to supposedly displace disease! It should be noted that hemp was also demonized and criminalized not long after this, not because there is anything dangerous about it, but because it was a huge threat (as both medicine and fuel) to the Rockefeller drug and oil industries, respectively.

The Rockefeller and Carnegie Tax-Exempt Foundations for “Efficient” Philanthropy

The story doesn’t stop there. Rockefeller and another elite leader Carnegie used their tax-exempt Foundations, from 1913 on, to offer huge grants to the best medical schools all over America – on the proviso that only an allopathic-based curriculum be taught, and that some of their agents be allowed to sit on the Board of Directors. They called this “efficient” philanthropy, which, when through the Orwellian translation unit, means they wanted a return on their investment. They systematically dismantled the curricula of these schools by removing any mention of the natural healing power of herbs and plants, or of the importance of diet to health. The result is a system which to this day churns out doctors who are, almost always, utterly clueless about nutrition and disregard the idea that what you eat can actually heal or hurt you.

A couple of decades after this, another law was passed that further entrenched western medicine in America. The Hill-Burton Act of 1946 gave hospitals grants for construction and modernization, on the condition they provide free healthcare to anyone in need, without discrimination of any kind. Although there were good sides to this, the downside was that once people had become dependent on this system for their healthcare needs – especially those on pharmaceutical pills which need to be taken day after day without end – the system switched into a paid system, and the Rockefellers found themselves with new lifelong customers.

The bitter truth is that, in general, when you go to your Western doctor, you are seen as a potential market for the medical factory’s products. For Big Pharma, there is no financial incentive to heal you, because a patient cured is a customer lost. Even if you are not sick, Big Pharma is still targeting you, trying to convince you that you are ill (e.g. with psychiatry’s ridiculous list of fictitious diseases, many of them fake) so that you will try its latest pill. Pregnant women who go to the doctor are treated like this, and peddled intravenous fluid bags, fetal monitors, ultrasound (radiation for a vulnerable baby), a host of drugs, the totally unnecessary episiotomy, and – to top it all off – the Caesarean delivery!

Bio-Piracy: The Business Model of Western Medicine’s Big Pharma Cartel

Remember, all these synthetic drugs are isolates. Many are derived from plant compounds, but because Nature cannot be patented and sold, Big Pharma has no interest in natural cures. What they do instead is engage in bio-piracy – research natural compounds, copy them (or modify them slightly) in a lab, then try to steal and patent them. If they get a patent, they then market their pill as a wonder drug while simultaneously (through fake scientific research) suppress and criticize the original plant as being worthless, so you won’t go to the source of the cure. Ironically, guess what type of medicine John D. Rockefeller used and the British Royal Family still uses? Homeopathy!

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Modern western medicine seems to have lost the supposed point of its existence: healing people. In his revealing book “Confessions of a Medical Heretic“, Dr. Robert Mendolsohn quotes an article entitled “Cleveland’s Marvelous Medical Factory” which boasted of the Cleveland Clinic’s “accomplishments last year: 2,980 open-heart operations, 1.3 million laboratory tests, 73,320 electrocardiograms, 7,770 full-body x-ray scans, 24,368 surgical procedures.” Seems fancy, yet none of these procedures has been proven to have anything to do with maintaining or restoring health. When people get screened for a disease, they are being subjected to dangerous radiation (more money for the Rockefellers) which harms tissue and can end up causing the exact disease it is supposed to be protecting against – as happens daily with the mammogram scam, designed to drum up new breast cancer clients.

western-medicine-rockefeller-medicine-john-d

John D. Rockefeller, the oil tycoon who helped create Big Pharma and Western Medicine.

Rockefeller Philanthropy is Social Control

The Rockefellers and other elites use philanthropy as a tool for control. It’s social engineering with a nice PR sheen. A free lunch is not really free, whether private (Rockefeller-style western medicine) or public/governmental (Obama-style socialized medicine), because even if you get something at no cost, you are required to give up your data and your privacy. They want you dependent on their system – then they’ll raise the rates once you’re trapped.

This is big business – and it’s also a big killer. Dr. Barbara Starfield published a study in the year 2000 that found that there were 225,000 iatrogenic (allopathic doctor caused) deaths in the US every year. However, this was only counting direct deaths; when you factor in all indirect deaths, as Dr. Gary Null did in 2011 in his report Death by Medicine, the figure is closer to 784,000 per year! That’s 7.8 million people dead from western medicine every 10 years!

Null concluded: “It is evident that the American medical system is the leading cause of death and injury in the United States …”

Whenever a lot of people die in a staged false flag attack (like 3000 people on 9/11) or in a staged mind control shooting (like 50 or so people) we hear all about it on the media. Yet between 616 and 2147 Americans are dying every day from Rockefeller Western medicine, and we don’t hear a thing!

Natural Solutions that Surpass Rockefeller-Created Western Medicine

At this point let us turn from the problem to the solutions – and fortunately there are many. The famous ancient Greek physician Hippocrates wrote:

“Nature heals. The doctor’s task consists in strengthening the natural healing powers, to direct them, and especially not to interfere with them.”

The immune system is your number one defense against any disease – not a vaccine. Most natural medicine is designed to treat the body holistically, not to “cure” one disease only to have it transform and mutate into another ailment. When you takes plants and herbs as medicine, you normally take the whole food, not an isolate, because it is based on a holistic understanding. Likewise, Traditional Chinese Medicine defines all disease as stagnation and treats sickness as an imbalance to be brought back into balance. What is the point of transferring an imbalance in one area into an imbalance in another area? None, unless you are trying to profit off disease like Big Pharma. It is not real healing.

There are so many natural cures and remedies out there, if you take the time to look. Two examples among thousands are turmeric which will do more for your blood pressure and diabetes than any drug can, and apricot kernels (rich in laetrile which selectively kills cancer cells and leaves healthy ones intact) which will handle cancer better than chemotherapy. The Gerson Therapy has also healed thousands of “terminal” cancer patients who were told by doctors of western medicine, “there’s nothing more we can do for you.”

Western medicine has its time and place, and its strengths and weaknesses. Western medicine may be a good system in a critical emergency and for complicated surgical procedures, but for general conditions, there are so many better alternatives. Time to start exploring them!

*****

Sources:

*https://thefreedomarticles.com/fluoride-fluoride-everywhere/

*https://thefreedomarticles.com/flexner-report-rockefeller-ama-takeover/

*https://thefreedomarticles.com/tax-exempt-foundations-rockefeller-fronts/

*https://thefreedomarticles.com/fictitious-diseases-psychiatry-big-pharma/

*http://www.whale.to/vaccines/mendelsohn2.html

*http://www.naturalnews.com/027641_mammograms_breast_cancer.html

*https://thefreedomarticles.com/obamacare-collectivist-medicine-at-gunpoint/

*http://www.drug-education.info/documents/iatrogenic.pdf

*http://www.webdc.com/pdfs/deathbymedicine.pdf

*http://gerson.org/gerpress/the-gerson-therapy

from:    https://thefreedomarticles.com/western-medicine-rockefeller-medicine/

Pay No Attention to he Facts

facebook

Facebook Labeling 100% Facts About Vaccine Company Corruption as ‘Misinformation’

The censors at Facebook’s ministry of truth have sunk to a new low. Yesterday at 1:35 p.m. EST, TFTP journalist Don Via Jr received a 24-hour ban on the platform for posting a completely factually accurate meme acknowledging big pharma’s history of rampant corruption.

Unlike other instances of individuals being censored on the platform however, in which the social media company attempts to thinly veil their censorship behind openly biased fact-checkers. This time there was none. No “fact check” for “false information”. Simply a notification of the post being removed from Mr. Via’s Break The Matrix Facebook page, and a notice that all of his accounts were restricted for 24 hours.

Below is the meme in question.

What makes this act of censorship particularly egregious is the blatant nature with which Facebook is now suppressing 100% verifiable facts.

After disputing the decision, Facebook replied with an automated message stating “We don’t allow false information that could cause physical harm. In some cases this includes information that recognized health organizations say could mislead people about how to cure or prevent a disease or that could discourage people from seeking medical treatment.”

In this case though, none of the information stated was false.

For instance, the first tier of the graphic claims that since inception in 1848, Pfizer has racked up nearly 5 billion dollars in criminal charges. While the exact total may vary a bit, the facts regarding their history of rampant corruption and medical malfeasance is.

In 1991, the FDA charged Pfizer subsidiary Shiley with withholding information from safety regulators and deliberately falsifying manufacturing records with regards to faulty heart valves. Nearly 300 people died from Pfizer’s faulty products and ultimately the company spent 205 million dollars settling the tens of thousands of lawsuits filed against them.

Despite this, Pfizer resisted to comply with FDA orders to notify patients and ultimately paid an additional $10 million when the Department of Justice charged them with lying to regulators.

In 2009, among other allegations of human rights abuses, Pfizer agreed to settle a lawsuit for $75 million after a lengthy court dispute in which it was charged with using Nigerian children as human guinea pigs.

In 2012 the company was forced to pay 60 million dollars after it was exposed for bribing foreign doctors to sell their products.

These are only a select few examples of the company’s history rife with criminal activity. More can be seen under Pfizer’s corporate rap sheet via the Corporate Research Project.

The second tier of the meme asserts that Moderna has not successfully completed the production of a viable vaccine in the company’s history. This can be confirmed via a simple internet search. In May of 2020, it was reported by The Daily Mail and CNN that Moderna has a track record of never bringing a successful vaccine to market since the company’s founding in 2010.

Furthermore, despite the company’s dubious past it was reported that Moderna was first tapped to lead U.S. vaccine development in what equated to a gamble. Simply because the company’s slick talking CEO was able to get the attention of former President Trump with bold promises during a meeting with biotech executives.

The third tier of the meme acknowledges the well-documented history of heinous crimes committed by Johnson & Johnson. Of which TFTP has also extensively covered in recent years.

As we reported in 2016, the company was forced to pay out billions of dollars in several lawsuits for continuing the sale of products they knew were causing cancer.

J&J has also been found guilty of irresponsible marketing practices and penalized nearly 600 million dollars for their role in fueling the opiate epidemic. As well as having been caught hiding crucial laboratory data from safety inspectors — resulting in the deaths of hundreds of people.

But these only scratch the surface of the company’s flagrant human rights abuses. Among them, being one of the main financiers alongside, Dow Chemical and the United States Army, funding 20 years of unethical human experiments by Dr. Albert Kligman in Pennsylvania’s Holmesburg prison. Experiments which entailed prisoners being financially coerced to “volunteer” as research subjects to study mind-altering drugs, painful medical procedures, radiation, and chemical weapons such as Agent Orange.

As a matter of fact, in addition to Pfizer and Johnson & Johnson — It is thoroughly documented by the Corporate Research Project that nearly every major company involved in the development of Covid-19 vaccines has an abhorrent history of medical malfeasance, and criminal charges.

Finally, the last section of the meme asserts that AstraZeneca’s covid-19 vaccine has itself already been suspended in 24 countries due to health concerns. Yet again, a simple query in your preferred search engine can corroborate this as a fact.

As a March 16th report from Al Jazeera explains; the countries of Sweden, Latvia, France, Germany, Italy, Spain, Luxembourg, Cyprus, Portugal, Slovenia, Indonesia, the Netherlands, Ireland, Bulgaria, the Democratic Republic of Congo, Thailand, Romania, Iceland, Denmark, Norway, and Austria have all suspended the Oxford / AstraZeneca jab in some capacity.

Since that report the Philippines and Australia have also suspended the shot for individuals under 60 years of age. Venezuela has also refused to authorize it.

What Facebook is doing by deleting this content, which by all accounts is completely accurate, is suppressing vital information that the people have a right to know. Informed consent matters, and it’s not something that can be so freely thrown to the wayside — certainly not as adverse events reported to the CDC are at an all-time high.

Facebook, as we have reported ad nauseam, works alongside government entities to facilitate their censorship. And more recently was even implicated in a lawsuit filed by Robert F Kennedy Jr as directly taking orders from the government to stifle concerns for vaccine safety on its platform.

The company is now essentially working as a cover-up crew to protect those with which they have a vested financial or political interest. While their counterparts in the mainstream media ingloriously propagate the notion that those concerned with vaccine safety are domestic terrorists.

Bodily autonomy is paramount, and individuals have an inherent right to be given all the facts so that they are adequately informed to make proper decisions with regard to their health.

Just because the truth is unpleasant, does not make it misinformation. As a matter of fact, censoring unpleasant truths in favor of biased one-sided narratives is the greatest danger of all.

from:   https://thefreethoughtproject.com/facebook-labeling-100-facts-about-vaccine-company-corruption-as-misinformation/

A New Washington Takes on Vested Interests

Senate meets AG nominee; treats her like lethal poison

by Jon Rappop

 

March 29, 2021

On January 29, 2027, the new president announced his choice for Attorney General, Claire Washington. Five days, later, she appeared at her confirmation hearing. Senator Grove Fatheringill III opened his folder and consulted his list of questions—

First of all, Ms. Washington, I want to offer my congratulations on your nomination. It’s about time we had another woman of color as—

Senator, I consider that an insult. I’m not here because I’m black. I’m here because the president thinks I’m qualified to serve. My skin is black. I was raised in what you could call “black culture.” But I’m my own person, which is to say, I’m an individual. My thoughts and actions aren’t black and they aren’t white. And frankly, I don’t care what people think of that remark. I’m not fronting for a particular culture. I happen to believe in the US Constitution. And if I may raise a few more hackles among those people waving their banners of political correctness, I am a sister to two brothers in my family, but I’m a not a “sister” to anyone else.

Ms. Washington, I didn’t mean to imply that as an African-American, you—

I’m not African American. My ancestors have lived in the United States for four generations. Are you British-American, Senator?

No. I was just…Ms. Washington, why don’t you tell us what your background…how your background and education equip you for the position of Attorney General?

I’m not sure they do. But I will say this. My first act upon gaining confirmation would be to pursue wide-ranging RICO cases against major gangs in the inner cities of America.

Excuse me, what?

Termination. Ending. Abolishment. Cancelation. Disbanding. Prosecution. Incarceration. Of gangs. As continuing criminal enterprises. Gangs continue to destroy the quality of life wherever they make their money.

What are the socio-economic causes that lead to the formation of gangs?

I’m interested in what the gangs are causing, as they sell toxic drugs, shoot and kill people, recruit innocent children into their ranks, destroy families, and make streets lethally unsafe.

But—

For decades, the Department of Justice has failed to mount RICO cases against gangs. Do you know why? Because the gangs sell drugs for cartels, and the cartels launder their money in banks. The cartels and the banks are protected, because IMPORTANT PEOPLE are making huge profits from the drug business. If you confirm me, all that will end like the snow ends when spring comes.

Are you accusing—

Yes, Senator, I am. Whoever you were about to ask me about, I am accusing them.

I didn’t even get a chance to—

My second line of attack will be against the CEOs of major corporations that pollute the environment—not with CO2—which is not killing anyone—but with highly dangerous chemicals. Certain key pesticides, for example.

However, you surely understand that modern industrial-scale agriculture—

And three, I will make sure pharmaceutical companies that sell highly toxic medicines are prosecuted to the fullest extent of the law, which means their CEOs will go to prison for very long terms.

Opioids, for example? Because we’re already—

Senator, this goes far beyond opioids. Every year in the US, FDA- approved drugs kill at least 100,000 people. That’s a million deaths per decade. Since the year 2000, when those numbers were published, the federal government has done NOTHING to remedy what amounts to a continuing holocaust. Under my administration, the complacence and negligence will end. I assure you.

But highly reputable medical journals publish studies of those drugs and—

The most prestigious journals are complicit in the continuing crime. They knowingly publish studies which are criminally deceptive. I will relentlessly prosecute their editors and reviewers.

Hold on. Are you talking about—

I’m talking about the New England Journal of Medicine, the Journal of the American Medical Association, and other publications. I’m also talking about FDA executives, who will become prime targets for DOJ prosecutions.

Criminal charges against—

Yes, Senator. Very serious criminal charges.

Ms. Washington, what about the guns? We have to take away the guns from people.

After every mass shooting, the usual politicians bray about taking guns away from the people who didn’t commit the crime. That’s not going to happen under my watch. I look at a map—as any citizen can—and I see where, in this country, people are shooting other people in large numbers. We will go into those areas and clean out the killers. The gangs.

That doesn’t make any sense.

It makes perfect sense. If America were attacked by China, would you want us to respond by assaulting Greenland?

China? My God, what are you talking about?

As any person with a few brain cells would understand, I was making a comparison to illustrate a point. I don’t envision an attack against the US from China.

The press and social media will be all over that China remark.

So what? The press and social media take perverse delight in twisting people’s statements. I don’t run my life by fear of what others will say. Do you?

Of course not. But—

Senator, I’ve just sketched out the top issues on my agenda. If you confirm me as the next Attorney General of the United States, you can expect to see action against those crimes from day one. And any prosecutor in the Department of Justice who doesn’t take my assignments seriously and honestly and with great zeal will be fired summarily. I want tigers, not house cats.

There are so many other crimes that need—

Yes there are. And I will go after the perpetrators. I don’t care what color their skin is. I don’t care where they live. I don’t care about their position in life or their reputation.

When it comes to protests in the streets of America—

If crimes are committed during these protests and riots, such as looting, burning, and assault, the states should arrest and prosecute the criminals. If they don’t, we will sue the states in court. If we find judges who refuse to hear our serious cases, we will do everything possible to bring those judges to justice.

Judges?? But there are many peaceful protests that—

Peaceful protests are of no concern, except when local law-enforcement tries to squash them for obvious political reasons. Then we would become involved. And I mean INVOLVED.

Ms. Washington, I want to return to the subject of opioids—

So do I, Senator. Because in 2016, both house of Congress passed a bill President Obama signed—and I know, for a fact, that the unanimous vote on that bill in both the House and the Senate was a sham, and virtually no one read the bill—

How can you say that?

Because it’s true. The bill, which became a law, has made it almost impossible for the DEA to enter the premises of pharmaceutical companies that are clearly TRAFFICKING opioids and put a stop to the crime of murder. It’s a detestable law. It’s called the Ensuring Patient Access and Effective Drug Enforcement Act of 2016, and it was signed by President Obama on 4/9/16. Perhaps you recall that the Washington Post ran an article on that opioid scandal.

I seem to remember—

The article mentioned an attempt was made to reach President Obama for a comment. He declined.

Ms. Washington, I don’t know about the other senators gathered here today, but I could never confirm you as the next Attorney General of the United States.

I assumed my confirmation would run into roadblocks. However, it occurs to me that the American people—many of them—would take a different view from yours. Who knows? If so, I suggest they contact your office.

Now wait a minute—

As we speak, several colleagues of mine are publishing, at my personal site, a list of all the bills you’ve voted to approve during your long and distinguished career in the Senate; and who, specifically, those votes benefited, and how much money in campaign donations you’ve accepted from those who’ve benefited. I assure you, the chart makes interesting reading.

THERE WAS AN UPROAR IN THE CHAMBER.

The networks cut the live feed.

Later that day, a bevy of reporters hungry for more red meat caught up with Claire Washington at her office. Before live television cameras, she said:

“Here it is, ladies and gentlemen. I don’t live or work on a plantation. Not in the fields, not in the house. I’m not black or white or red or yellow or purple or blue. I’m a free American. My only standard is the Constitution. For decades, the Department of Justice has served special interests. Under my watch, all that would end. I don’t fear the biggest corporate CEOs in the country, or the lowest gang killers in Chicago, or US Senators. If you want a racket and crime busting Attorney General, here I am. My bloodhound law partners are already preparing a case against Pfizer and Moderna for lying to the public about the safety and efficacy of their COVID vaccines—“

The television networks cut the live feed again.

But they had a bit of the problem, as they would discover in the next few days. Whenever the face of Claire Washington appeared on screens, ratings shot up to all-time levels…

Twitter, Facebook, YouTube, and other social media rabidly deleted posts that supported the AG nominee, but it didn’t seem to matter.

As Chris Wallace of FOX commented, “Something in the soul of American culture has been unleashed. We don’t know what it is, but it’s moving up and out like a hurricane. We’d probably like to say it’s a rerun of the Trump effect, but it’s bigger than that…”

Two weeks later, with the Senate confirmation hearings still in mysterious adjournment, Claire Washington sat down for an interview with 60 Minutes’ Tom Dooley. She jumped in with both feet:

“Censorship has overtaken America, Tommy. If I win appointment as the next Attorney General—and opinion polls are showing the American people want me in that office—I’m going to go after social media giants with a vengeance. They’re the public square and the town hall, whether they like it or not, and they have no right to set off a bomb in the middle of the 1st Amendment. Frankly, these CEOs are some of the scummiest aristocrats I’ve ever come across. I’ll tell you a little secret. Ending censorship would eventually put social media operations in a hole. With an adequate spread of opinion across the whole cultural and political spectrum, tension and drama would deflate like an old bag. Finally, nobody would care. It’s censorship that actually drives the popularity of these sleazy social media outfits…”

Mark Zuckerberg and his wife promptly left the country for a visit to China.

from:    https://blog.nomorefakenews.com/2021/03/29/senate-meets-ag-nominee-treats-her-like-lethal-poison/

Who Benefits?

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.

from:    https://childrenshealthdefense.org/defender/medical-racism-film-exposes-experimentation-minorities/?utm_source=salsa&eType=EmailBlastContent&eId=bbb5bc07-f2eb-4a23-9c99-6a47b24b9753

And Now, Embassies and Military Bases in Exchange for Vaccine

Conspiracy Theater

THE PLANSCAMDEMIC’S LATEST TWISTED TWIST

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:

How Pfizer tried to bully Argentina and Brazil in exchange for vaccines

‘Held to ransom’: Pfizer demands governments gamble with state assets to secure vaccine deal

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.

See you on the flip side…

from:    https://gizadeathstar.com/2021/03/the-planscamdemics-latest-twisted-twist/

A Little Shot of Cancer, Perhaps?

(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


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.

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.

FDA as an arm of Big Pharma

Between 2000 and 2010, pharmaceutical companies paid the FDA $3.4 billion to gain rapid drug approvals. Today, Pharma companies underwrite three-quarters of FDA’s budget for scientific reviews (ProPublica) and fund nearly 50% of the FDA’s total annual budget through PDUFA fees. In exchange, the agency increasingly fast-tracks expensive drugs and vaccines with significant side effects and unproven health benefits.

Corrupt vaccine approval panels

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:

  1. “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.
  2. “One out of five voting members’ employer had a $9,586,000 contract for a rotavirus vaccine.
  3. “One out of five voting members was the principal investigator for a Merck grant to develop a rotavirus vaccine.
  4. “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.

The HeLa cells are well known to cause cancer in animals, but Big Pharma wanted to lower production costs of vaccines and this method is cheaper and faster than using animal tissue for the cultivated media. …

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.

FDA officials knew that tumors might occur decades after vaccination.

FDA openly acknowledged that its primary objective was not to assure public safety but to help vaccine manufacturers.

FDA officials knew that they could not prove vaccine safety using test animals to assess oncogenicity.

FDA officials deliberately terminated animal safety tests too early in order to conceal consequences.

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.

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.

FDA decided to hide information about their use of tumor cells and omit it from package inserts. 

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.

FDA officials opted to toss the dice, perform the population-wide human experiment, and learn about the risks as time goes by.

The committee formally approves the method of making vaccines from human cancer tumors.

..

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.

from:    https://childrenshealthdefense.org/defender/fda-cancer-cells-in-vaccines/?utm_source=salsa&eType=EmailBlastContent&eId=8fc80363-cace-4de1-bcd2-9e309b779ac5

THey Will Pay You to Vaccinate Your Child

FDA Lets Pfizer Test Experimental COVID-19 Vaccine on U.S. Children

Pfizer becomes first company in U.S. to include children in Phase 3 COVID vaccine trials.

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?

from:    https://childrenshealthdefense.org/defender/fda-pfizer-experimental-covid-vaccine-children/?utm_source=salsa&eType=EmailBlastContent&eId=b18c0c6e-fe4c-4d23-b98f-d41da6147716

The More You Know – Support Those Who Fight For The Truth

6 Wikileaks Revelations Expose Corporate Abuse At The Expense of People & Planet

By. 

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 ongoing persecution 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 series accusing 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.

Written by Jeremy Loffredo.

from:     https://www.collective-evolution.com/2020/10/06/6-wikileaks-revelations-expose-corporate-abuse-at-the-expense-of-people-planet/

Worth A Read & Honest Consideration – Especially if You Want A Vaccine

The Injection Fraud – It’s Not a Vaccine

“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)

Aborted fetal tissue, animal tissue, aluminum, mercury, genetically altered materials—and what else?

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.

“THEY” Do Not Want an Effective and Inexpensive Treatment -No $$$ For Them

An Effective COVID Treatment the Media Continues to Besmirch

August 04, 2020

An Effective COVID Treatment the Media Continues to Besmirch
(AP Photo/Rafiq Maqbool)

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 early phase 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 May  27 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.

from:    https://www.realclearpolitics.com/articles/2020/08/04/an_effective_covid_treatment_the_media_continues_to_besmirch_143875.html