The Pushing for Coronavirus Vaccines

Neo 18.05.2020

The US White House has appointed a coronavirus “Vaccine Czar” from Big Pharma to oversee something dubbed Operation Warp Speed. The goal is to create and produce 300 million doses of a new vaccine to supposedly immunize the entire US population by year-end against COVID-19. To be sure that Big Pharma companies give their all to the medical Manhattan Project, they have been fully indemnified by the US government against liabilities should vaccine recipients die or develop serious disease as a result of the rushed vaccine. The FDA and NIH have waived standard pre-testing on animals in the situation. The US military, according to recent remarks by the US President, is being trained to administer the yet-to-be unveiled vaccine in record time. Surely nothing could go wrong here?

Warp speed is a term out of the sci-fi Star Trek media, defined as a speed faster than the speed of light. In recent weeks billions of dollars have been pledged from governments, from the Bill and Melinda Gates Foundation and others to fast-track a vaccine as well as test medical treatments to combat the VODIV19 illness said to originate from a novel coronavirus first discovered late 2019 in Wuhan China. This rush to create a “miracle” vaccine is ominous and suggests some hidden agenda.

FDA Study: Cells Used In Vaccines Contaminated With Serious Viruses Including Cancer

Activist Post 23 Nov 2019

The U.S. Food and Drug Administration (FDA) has published shocking results which found that cells used in the manufacturing of numerous childhood vaccines are often contaminated with serious viruses including cancer.

The FDA study looked at vaccines that are made from living cells, or replicated cell substrates that some manufacturers are investigating to create. According to research, these cells are oftentimes contaminated with hidden viral fragments which have the potential to cause cancer.

These viruses are dormant, meaning they live “quietly” inside other cells. However, eventually these cells no longer hide and circulate throughout the body in the form of serious disease. As a result, a person injected with a vaccine containing these cancer-causing micro-organisms may not display signs of health complications until long after they have been jabbed sometimes several years later.

First GMO rice from china just approved by FDA

Natural Blaze   January 23, 2018

As we reported last summer, Big Agri pulled some maneuvers and made major inroads in China despite major opposition from China’s people. Readers may be surprised to learn that Chinese citizens reject the notion of GMOs but they do. In fact, there is such a demand for organic there, that China is buying up arable land in other countries and trumpeting health campaigns to discourage meat and dairy consumption. Not only has this demand for better food caused food shortages there because of their issues with pollution, but it has also created a bevy of “fake organics” and questionable foods flooding other countries. Are we about to receive a flood of GM rice, too?

Now the FDA has essentially approved a product based on some data turned in by Chinese researchers. It did not conduct its own experiments. Although cultivation of this GM rice is not officially legal, the FDA stamp of approval was meant to set the ball rolling, and garner approval from other markets.

GlobalTimes.CN reports:

A genetically modified (GM) rice product developed by a group of Chinese scientists has acquired the US Food and Drug Administration (FDA) approval, the first such Chinese product allowed to enter the US market.

However, neither China nor the US has approved mass cultivation of the rice amid low acceptance from the Chinese public for GM food.

Huahui No.1 rice, developed by the Huazhong Agricultural University, is genetically engineered to resist a wide range of insects, thus reducing the use of pesticides.

Monsanto’s Cancer-Causing Herbicide Detected In Organic Foods

Michelle Toole

Think you can avoid glyphosate by buying organic? Think again. A new investigation by Tropical Traditions reveals that many products in the organic grain market in the U.S. contain glyphosate residue at levels almost the same as conventional grains.

You and your loved ones likely ingested Monsanto’s cancer-causing herbicide with breakfast this morning and the FDA couldn’t care less.

The FDA is demonstrating their incompetence yet again by completely ignoring a critical report that shows how ubiquitous Monsanto’s carcinogenic Roundup has truly become.

According to the report released by the Alliance for Natural Health USA, detectable levels of glyphosate, the chief ingredient in Roundup, were found in numerous breakfast food items. Glyphosate, which has been linked to cancer by the World Health Organization, was found in bread products, cereals and coffee creamers.

What is really concerning, and exemplifies the need for an immediate ban on the carcinogenic herbicide, is that some of the highest levels of the toxic chemical were found in organic foods, such as eggs and breads. The organic eggs tested were especially tainted with glyphosate, far exceeding regulatory standards.

Microbe Infotech Laboratories, founded by former Monsanto scientist Bruce Hemming, conducted the testing. For 25 years, Microbe has been well-respected and is the go-to lab for glyphosate testing by food companies and consumer groups.

The report confirms what many have feared for a long time. Glyphosate is making its way into our food in ways that we may not realize. For example, last year a separate study found 75% of rain and air samples tested positive for Monsanto’s cancer-causing poison. What kind of ramifications do you think this will have for those growing organic gardens? (via march against monsanto)

“The fact that it is showing up in foods like eggs and coffee creamer, which don’t directly contact the herbicide, shows that it’s being passed on by animals who ingest it in their feed,” said Gretchen DuBeau, executive director of ANH-USA. “This is contrary to everything that regulators and industry scientists have been telling the public.”

Why Should We be Concerned about Glyphosate?

Glyphosate is in 80% of our food supply in the U.S., and some scientists believe it may well be the most toxic chemical ever approved for commercial use. Glyphosate is now linked to kidney disease, antibiotic resistant bacteria, inflammatory bowel disease, obesity, depression, ADHD, autism, Alzheimer’s disease, Parkinson’s disease, ALS, multiple sclerosis, cancer, cachexia, infertility, and developmental malformations. It destroys the microbiome of humans and plants, which is the root cause of many modern diseases.(health impact news)       HHL

Use of Term “FDA” Should Always Trigger a Warning

Posted on June 6, 2016  By Jon Rappoport

“In 1957, the FDA burned all the books of dissident physician Wilhelm Reich, M.D., smashed his laboratory equipment with axes, and threw him in jail, where he died.”—Robert Anton Wilson, High Times, March 2001.

Unless you’ve been living in cave on a remote mountain, you know the FDA has been coming down harder on nutritional companies that publish health claims for their products. Such claims trigger investigations and harassment.

But you see, this arrangement is backwards.

The use of the term “FDA” should be the trigger for immediate investigation, whenever it appears. For example, “The FDA has ruled (name of drug) is safe and effective.” Boom. Probe.

Why? Obviously, the FDA is a rogue criminal organization, which is guilty of massive RICO felonies. That’s why.

A news story mentioning the FDA appears in a major newspaper? The paper, if it has an approximation of ethical concern, should print this:

“Warning: any action attributed to the FDA should be considered criminal. Accepting an FDA opinion on something more serious than ‘H2O=water’ endangers life and limb. This news outlet accepts no responsibility for the health consequences of any FDA decision.”

Now we’d be on the right track.

July 26, 2000, Journal of the American Medical Association, Dr. Barbara Starfield, Johns Hopkins School of Public Health, “Is US health really the best in the world?”: Medical drugs kill 106,000 Americans per year. That’s a million killings per decade.

Every one of the killer drugs is certified as safe and effective by the FDA, the Agency tasked with protecting the health of the American people.

Example: Vioxx was approved for use by the FDA on May 20, 1999. Eventually, it caused 88,000-140,000 cases of heart disease. Conservative death-toll number? 60,000. (An estimated 58,000 American troops died during the Vietnam War.)

“Warning: If you accept the FDA’s advice on a health matter, you’re risking death. In case there is any confusion, death means death.”

“Did you just read a statement from the FDA? Your life is in imminent danger.”

Perhaps you recall the original approval of GMO crops and their associated highly toxic Roundup pesticide? No? Let me summarize it for you.

When you cut through the verbiage, you arrive at two key statements. One from Monsanto and one from the FDA, the agency responsible for overseeing, licensing, and certifying new food varieties as safe.

Quoted in the New York Times Magazine (October 25, 1998, “Playing God in the Garden”), Philip Angell, Monsanto’s director of corporate communications, famously stated:

“Monsanto shouldn’t have to vouchsafe the safety of biotech food. Our interest is in selling as much of it as possible. Assuring its safety is the FDA’s job.”

From the Federal Register, Volume 57, No.104, “Statement of [FDA] Policy: Foods Derived from New Plant Varieties,” here is what the FDA had to say on this matter:

“Ultimately, it is the food producer who is responsible for assuring safety.”

The buck-passing, the direct and irreconcilable clash of these two statements, is no accident. It’s not a sign of incompetence or sloppy work or a mistake or a miscommunication. It’s a clear signal the fix was in.

“Warning: The relationship of an FDA certification of safety to actual science is coincidental. Run for the hills.”

In a stunning interview with Truthout’s Martha Rosenberg, former FDA drug reviewer, Ronald Kavanagh, exposed the FDA as a relentless criminal mafia protecting its client, Big Pharma, with a host of mob strategies (“Former FDA Reviewer Speaks Out About Intimidation, Retaliation and Marginalizing of Safety,” 7/29/2012).

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Kavanagh: “…widespread racketeering, including witness tampering and witness retaliation.”

“I was threatened with prison.”

“One [FDA] manager threatened my children…I was afraid that I could be killed for talking to Congress and criminal investigators.”

Kavanagh reviewed new drug applications made to the FDA by pharmaceutical companies. He was one of the holdouts at the Agency who insisted the drugs had to be safe and effective before being released to the public.

But honest appraisal wasn’t part of the FDA culture, and Kavanagh swam against the tide, until he realized his life and the life of his children was on the line.

What was his secret task at the FDA? “Drug reviewers were clearly told not to question drug companies and that our job was to approve drugs.” In other words, rubber stamp them. Say the drugs were safe and effective when they were not.

Veterans of the Armed Forces, take note: Kavanagh remarks that the drug pyridostigmine, given to US troops to prevent the later effects of nerve gas, “actually increased the lethality” of certain nerve agents.

Kavanagh recalls being given records of safety data on a drug—and then his bosses told him which sections not to read. Obviously, they knew the drug was dangerous and they knew exactly where, in the reports, that fact would be revealed.

“Warning: the FDA hammers into submission its own employees who are trying to protect your health. These employees submit, resign, or risk their lives and the lives of their families. Have a nice day.”

Of course, the US Department of Justice takes no action against the FDA. Why would they?

In the government lexicon, killer medical drug equals safe and effective, whereas vitamin, mineral, herb equals H-bomb. Didn’t you know that?

“Warning: FDA killers resemble ordinary citizens. They appear entirely normal. Their methods have advanced to the point where they can commit their deeds without brandishing visible weapons.”

“—Hi, I’m from the FDA. Hey, why are you running away? I’m a public servant doing his job. Gosh o gee, I’m just like you.”

Yes, they can affect an entirely average presence. They internally censor remorse for their crimes. They commit those crimes while pretending to believe they’re carrying out important work. I don’t know why the CIA and DARPA keep researching more advanced forms of mind control. They merely need to study the FDA. That Agency has it down.

“Warning: failing to heed warnings about the FDA is a symptom of advanced dementia.”     Natural Blaze