Tag Archives: FDA

US – UK Intel Agencies Declare Cyber War on Independent Media

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British and American state intelligence agencies are “weaponizing truth” to quash vaccine hesitancy as both nations prepare for mass inoculations, in a recently announced “cyber war” to be commanded by AI-powered arbiters of truth against information sources that challenge official narratives.

By Whitney Webb

Source: Unlimited Hangout

In just the past week, the national-security states of the United States and United Kingdom have discreetly let it be known that the cyber tools and online tactics previously designed for use in the post-9/11 “war on terror” are now being repurposed for use against information sources promoting “vaccine hesitancy” and information related to Covid-19 that runs counter to their state narratives.

A new cyber offensive was launched on Monday by the UK’s signal intelligence agency, Government Communications Headquarters (GCHQ), which seeks to target websites that publish content deemed to be “propaganda” that raises concerns regarding state-sponsored Covid-19 vaccine development and the multi-national pharmaceutical corporations involved.

Similar efforts are underway in the United States, with the US military recently funding a CIA-backed firm—stuffed with former counterterrorism officials who were behind the occupation of Iraq and the rise of the so-called Islamic State—to develop an AI algorithm aimed specifically at new websites promoting “suspected” disinformation related to the Covid-19 crisis and the US military–led Covid-19 vaccination effort known as Operation Warp Speed.

Both countries are preparing to silence independent journalists who raise legitimate concerns over pharmaceutical industry corruption or the extreme secrecy surrounding state-sponsored Covid-19 vaccination efforts, now that Pfizer’s vaccine candidate is slated to be approved by the US Food and Drug Administration (FDA) by month’s end.

Pfizer’s history of being fined billions for illegal marketing and for bribing government officials to help them cover up an illegal drug trial that killed eleven children (among other crimes) has gone unmentioned by most mass media outlets, which instead have celebrated the apparently imminent approval of the company’s Covid-19 vaccine without questioning the company’s history or that the mRNA technology used in the vaccine has sped through normal safety trial protocols and has never been approved for human use. Also unmentioned is that the head of the FDA’s Center for Drug Evaluation and Research, Patrizia Cavazzoni, is the former Pfizer vice president for product safety who covered up the connection of one of its products to birth defects.

Essentially, the power of the state is being wielded like never before to police online speech and to deplatform news websites to protect the interests of powerful corporations like Pfizer and other scandal-ridden pharmaceutical giants as well as the interests of the US and UK national-security states, which themselves are intimately involved in the Covid-19 vaccination endeavor.

UK Intelligence’s New Cyberwar Targeting “Anti-Vaccine Propaganda”

On Monday, the UK newspaper The Times reported that the UK’s GCHQ “has begun an offensive cyber-operation to disrupt anti-vaccine propaganda being spread by hostile states” and “is using a toolkit developed to tackle disinformation and recruitment material peddled by Islamic State” to do so. In addition, the UK government has ordered the British military’s 77th Brigade, which specializes in “information warfare,” to launch an online campaign to counter “deceptive narratives” about Covid-19 vaccine candidates.

The newly announced GCHQ “cyber war” will not only take down “anti-vaccine propaganda” but will also seek to “disrupt the operations of the cyberactors responsible for it, including encrypting their data so they cannot access it and blocking their communications with each other.”  The effort will also involve GCHQ reaching out to other countries in the “Five Eyes” alliance (US, Australia, New Zealand and Canada) to alert their partner agencies in those countries to target such “propaganda” sites hosted within their borders.

The Times stated that “the government regards tackling false information about inoculation as a rising priority as the prospect of a reliable vaccine against the coronavirus draws closer,” suggesting that efforts will continue to ramp up as a vaccine candidate gets closer to approval.

It seems that, from the perspective of the UK national-security state, those who question corruption in the pharmaceutical industry and its possible impact on the leading experimental Covid-19 vaccine candidates (all of which use experimental vaccine technologies that have never before been approved for human use) should be targeted with tools originally designed to combat terrorist propaganda.

While The Times asserted that the effort would target content “that originated only from state adversaries” and would not target the sites of “ordinary citizens,” the newspaper suggested that the effort would rely on the US government for determining whether or not a site is part of a “foreign disinformation” operation.

This is highly troubling given that the US recently seized the domains of many sites, including the American Herald Tribune, which it erroneously labeled as “Iranian propaganda,” despite its editor in chief, Anthony Hall, being based in Canada. The US government made this claim about the American Herald Tribune after the cybersecurity firm FireEye, a US government contractor, stated that it had “moderate confidence” that the site had been “founded in Iran.”

In addition, the fact that GCHQ has alleged that most of the sites it plans to target are “linked to Moscow” gives further cause for concern given that the UK government was caught funding the Institute for Statecraft’s Integrity Initiative, which falsely labeled critics of the UK government’s actions as well as its narratives with respect to the Syria conflict as being related to “Russian disinformation” campaigns.

Given this precedent, it is certainly plausible that GCHQ could take the word of either an allied government, a government contractor, or perhaps even an allied media organization such as Bellingcat or the Atlantic Council’s DFRLab that a given site is “foreign propaganda” in order to launch a cyber offensive against it. Such concerns are only amplified when one of the main government sources for The Times article bluntly stated that “GCHQ has been told to take out antivaxers [sic] online and on social media. There are ways they have used to monitor and disrupt terrorist propaganda,” which suggests that the targets of GCHQ’s new cyber war will, in fact, be determined by the content itself rather than their suspected “foreign” origin. The “foreign” aspect instead appears to be a means of evading the prohibition in GCHQ’s operational mandate on targeting the speech or websites of ordinary citizens.

This larger pivot toward treating alleged “anti-vaxxers” as “national security threats” has been ongoing for much of this year, spearheaded in part by Imran Ahmed, the CEO of the UK-based Center for Countering Digital Hate, a member of the UK government’s Steering Committee on Countering Extremism Pilot Task Force, which is part of the UK government’s Commission for Countering Extremism.

Ahmed told the UK newspaper The Independent in July that “I would go beyond calling anti-vaxxers conspiracy theorists to say they are an extremist group that pose a national security risk.” He then stated that “once someone has been exposed to one type of conspiracy it’s easy to lead them down a path where they embrace more radical world views that can lead to violent extremism,” thereby implying that “anti-vaxxers” might engage in acts of violent extremism. Among the websites cited by Ahmed’s organization as promoting such “extremism” that poses a “national security risk” were Children’s Health Defense, the National Vaccine Information Center, Informed Consent Action Network, and Mercola.com, among others.

Similarly, a think tank tied to US intelligence—whose GCHQ equivalent, the National Security Agency, will take part in the newly announced “cyber war”—argued in a research paper published just months before the onset of the Covid-19 crisis that “the US ‘anti-vaxxer’ movement would pose a threat to national security in the event of a ‘pandemic with a novel organism.’”

InfraGard, “a partnership between the Federal Bureau of Investigation (FBI) and members of the private sector,” warned in the paper published last June that “the US anti-vaccine movement would also be connected with ‘social media misinformation and propaganda campaigns’ orchestrated by the Russian government,” as cited by The Guardian. The InfraGard paper further claimed that prominent “anti-vaxxers” are aligned “with other conspiracy movements including the far right . . . and social media misinformation and propaganda campaigns by many foreign and domestic actors. Included among these actors is the Internet Research Agency, the Russian government–aligned organization.”

An article published just last month by the Washington Post argued that “vaccine hesitancy is mixing with coronavirus denial and merging with far-right American conspiracy theories, including Qanon,” which the FBI named a potential domestic terror threat last year. The article quoted Peter Hotez, dean of the School of Tropical Medicine at Baylor College of Medicine in Houston, as saying “The US anti-vaccination movement is globalizing and it’s going toward more-extremist tendencies.”

It is worth pointing out that many so-called “anti-vaxxers” are actually critics of the pharmaceutical industry and are not necessarily opposed to vaccines in and of themselves, making the labels “anti-vaxxer” and “anti-vaccine” misleading. Given that many pharmaceutical giants involved in making Covid-19 vaccines donate heavily to politiciansin both countries and have been involved in numerous safety scandals, using state intelligence agencies to wage cyber war against sites that investigate such concerns is not only troubling for the future of journalism but it suggests that the UK is taking a dangerous leap toward becoming a country that uses its state powers to treat the enemies of corporations as enemies of the state.

The CIA-Backed Firm “Weaponizing Truth” with AI

In early October, the US Air Force and US Special Operations Command announced that they had awarded a multimillion-dollar contract to the US-based “machine intelligence” company Primer. Per the press release, “Primer will develop the first-ever machine learning platform to automatically identify and assess suspected disinformation [emphasis added]. Primer will also enhance its natural language processing platform to automatically analyze tactical events to provide commanders with unprecedented insight as events unfold in near real-time.”

According to Primer, the company “builds software machines that read and write in English, Russian, and Chinese to automatically unearth trends and patterns across large volumes of data,” and their work “supports the mission of the intelligence community and broader DOD by automating reading and research tasks to enhance the speed and quality of decision-making.” In other words, Primer is developing an algorithm that would allow the national-security state to outsource many military and intelligence analyst positions to AI. In fact, the company openly admits this, stating that their current effort “will automate the work typically done by dozens of analysts in a security operations center to ingest all of the data relevant to an event as it happens and funnel it into a unified user interface.”

Primer’s ultimate goal is to use their AI to entirely automate the shaping of public perceptions and become the arbiter of “truth,” as defined by the state. Primer’s founder, Sean Gourley, who previously created AI programs for the military to track “insurgency” in post-invasion Iraq, asserted in an April blog post that “computational warfare and disinformation campaigns will, in 2020, become a more serious threat than physical war, and we will have to rethink the weapons we deploy to fight them.”

In that same post, Gourley argued for the creation of a “Manhattan Project for truth” that would create a publicly available Wikipedia-style database built off of “knowledge bases [that] already exist inside many countries’ intelligence agencies for national security purposes.” Gourley then wrote that “this effort would be ultimately about building and enhancing our collective intelligence and establishing a baseline for what’s true or not” as established by intelligence agencies. He concludes his blog post by stating that “in 2020, we will begin to weaponize truth.”

Notably, on November 9, the same day that GCHQ announced its plans to target “anti-vaccine propaganda,” the US website NextGov reported that Primer’s Pentagon-funded effort had turned its attention specifically to “Covid-19 related disinformation.” According to Primer’s director of science, John Bohannon, “Primer will be integrating bot detection, synthetic text detection and unstructured textual claims analysis capabilities into our existing artificial intelligence platform currently in use with DOD. . . . This will create the first unified mission-ready platform to effectively counter Covid-19-related disinformation in near-real time.”

Bohannon, who previously worked as a mainstream journalist embedded with NATO forces in Afghanistan, also told NextGov that Primer’s new Covid-19–focused effort “automatically classifies documents into one of 10 categories to enable the detection of the impact of COVID” on areas such as “business, science and technology, employment, the global economy, and elections.” The final product is expected to be delivered to the Pentagon in the second quarter of next year.

Though a so-called private company, Primer is deeply linked to the national-security state it is designed to protect by “weaponizing truth.” Primer proudly promotes itself as having more than 15 percent of its staff hailing from the US intelligence community or military. The director of the company’s National Security Group is Brian Raymond, a former CIA intelligence officer who served as the Director for Iraq on the US National Security Council after leaving the agency.

The company also recently added several prominent national-security officials to its board including:

  • Gen. Raymond Thomas (ret.), who led the command of all US and NATO Special Operations Forces in Afghanistan and is the former commander of both US Special Operations Command and Joint Special Operations Command (JSOC).
  • Lt. Gen. VeraLinn Jamieson (ret.), the former deputy chief of staff for Air Force Intelligence, Surveillance and Reconnaissance who led the Air Force’s intelligence and cyber forces. She also personally developed “strategic partnerships” between the Air Force and Microsoft, Amazon, Google, and IBM in order “to accelerate the Air Force’s digital transformation.”
  • Brett McGurk, one of the “chief architects” of the Iraq War “surge,” alongside the notorious Kagan family, as NSC Director for Iraq, and then as special assistant to the president and senior Director for Iraq and Afghanistan during the Bush administration. Under Obama and during part of the Trump administration, McGurk was the special presidential envoy for the Global Coalition to Defeat ISIS at the State Department, helping to manage the “dirty war” waged by the US, the UK, and other allies against Syria.

In addition to those recent board hires, Primer brought on Sue Gordon, the former principal deputy director of National Intelligence, as a strategic adviser. Gordon previously “drove partnerships within the US Intelligence Community and provided advice to the National Security Council in her role as deputy director of national intelligence” and had a twenty-seven-year career at the CIA. The deep links are unsurprising, given that Primer is financially backed by the CIA’s venture-capital arm In-Q-Tel and the venture-capital arm of billionaire Mike Bloomberg, Bloomberg Beta.

Operation Warp Speed’s Disinformation Blitzkrieg

The rapid increase in interest by the US and UK national-security states toward Covid-19 “disinformation,” particularly as it relates to upcoming Covid-19 vaccination campaigns, is intimately related to the media-engagement strategy of the US government’s Operation Warp Speed.

Officially a “public-private partnership,” Operation Warp Speed, which has the goal of vaccinating 300 million Americans by next January, is dominated by the US military and also involves several US intelligence agencies, including the National Security Agency (NSA) and the Department of Homeland Security (DHS), as well as intelligence-linked tech giants Google, Oracle, and Palantir. Several reports published in The Last American Vagabondby this author and journalist Derrick Broze have revealed the extreme secrecy of the operation, its numerous conflicts of interest, and its deep ties to Silicon Valley and Orwellian technocratic initiatives.

Warp Speed’s official guidance discusses at length its phased plan for engaging the public and addressing issues of “vaccine hesitancy.” According to the Warp Speed document entitled “From the Factory to the Frontlines,” “strategic communications and public messaging are critical to ensure maximum acceptance of vaccines, requiring a saturation of messaging across the national media.” It also states that “working with established partners—especially those that are trusted sources for target audiences—is critical to advancing public understanding of, access to, and acceptance of eventual vaccines” and that “identifying the right messages to promote vaccine confidence, countering misinformation, and targeting outreach to vulnerable and at-risk populations will be necessary to achieve high coverage.”

The document also notes that Warp Speed will employ the CDC’s three-pronged strategic framework for its communications effort. The third pillar of that strategy is entitled “Stop Myths” and has as a main focus “establish[ing] partnerships to contain the spread of misinformation” as well as “work[ing] with local partners and trusted messengers to improve confidence in vaccines.”

Though that particular Warp Speed document is short on specifics, the CDC’s Covid-19 Vaccination Program Interim Playbook contains additional information. It states that Operation Warp Speed will “engage and use a wide range of partners, collaborations, and communication and news media channels to achieve communication goals, understanding that channel preferences and credible sources vary among audiences and people at higher risk for severe illness and critical populations, and channels vary in their capacity to achieve different communication objectives.” It states that it will focus its efforts in this regard on “traditional media channels” (print, radio, and TV) as well as “digital media” (internet, social media, and text messaging).

The CDC document further reveals that the “public messaging” campaign to “promote vaccine uptake” and address “vaccine hesitancy” is divided into four phases and adds that the overall communication strategy of Warp Speed “should be timely and applicable for the current phase of the Covid-19 Vaccination program.”

Those phases are:

  • Before a vaccine is available
  • The vaccine is available in limited supply for certain populations of early focus
  • The vaccine is increasingly available for other critical populations and the general public
  • The vaccine is widely available

Given that the Covid-19 vaccine candidate produced by Pfizer is expected to be approved by the end of November, it appears that the US national-security state, which is essentially running Operation Warp Speed, along with “trusted messengers” in mass media, is preparing to enter the second phase of its communications strategy, one in which news organizations and journalists who raise legitimate concerns about Warp Speed will be de-platformed to make way for the “required” saturation of pro-vaccine messaging across the English-speaking media landscape.

HOW THEY’LL FAKE THE SUCCESS OF THE COVID VACCINE

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By Jon Rappoport

Source: Waking Times

I’ve described how the major clinical trials of the COVID vaccine are designed to prevent nothing more than a cough, or chills and fever [1] [2].

The whole plan to gain FDA approval of the vaccine is a stark fraud.

Now let’s move on to the next con: how to make it seem the vaccine is a roaring success.

Brief background: My readers know I’ve presented a complete case to show the SARS-CoV-2 virus was never proved to exist in the first place [3] [4] [5] [6] [7] [8] [9] [10]. So the whole idea of a vaccine is a non-sequitur, an absurdity. Likewise, the PCR test for “the virus” is a fraud on several levels [11]:

For example, the number of “cycles” for which the test is set is a key factor. Each cycle is a huge amplification of the tissue sample taken from the patient.

When you blow up that tissue sample above 34 cycles, you get gigantic numbers of false-positive results, even by the standards of the test. Fauci has admitted it. I’ve pointed out that FDA guidelines nevertheless recommend doing the test at up to 40 cycles. This alone explains reports of “rising COVID case numbers.”

Let’s say Pfizer and then Moderna win FDA approval to release their vaccines in the US. With the military doing the logistics of shipping, millions of doses move out, and soon, an extraordinary number of Americans are lining up to take the shot.

After a suitable period of time, the elite medical planners will change the way the PCR test is done. The number of cycles will be drastically reduced. That order will go out to labs in the US.

What does this mean? It means that far fewer positive test results will occur.

Therefore, the trend of “new COVID cases” will stop rising. It will level off, and then it will fall.

This rigging will be heralded as proof that that vaccine is producing a victory over the virus.

There is another strategy: change the definition of “a case of COVID.” Make the new definition, in terms of clinical symptoms, more restrictive. Something like this would do the trick: “The patient must exhibit a body temperature of at least 100 for 48 consecutive hours.”

That will automatically cause a significant drop in the number of cases. The drop will be attributed to the salutary effect of the vaccine.

For purposes of lockdowns and general clampdowns [12], to promote more fear and punish areas where the economy is “too open,” a reverse-technique can be applied:

Make PCR tests adjust their cycles UPWARD, thus producing huge numbers of positive results and “new cases.”

“Well, in South Dakota, we have to mandate at least 100,000 more vaccinations in each of the following ‘hot spots,’ where case numbers have suddenly escalated. And we must lock down those areas immediately…”

Needless to say, any and all serious harm and death caused by the vaccine anywhere will be attributed to “the pandemic disease.”

And there you have it. Simple, brutal, criminal, and controlled from the federal level. A strategy for making it seem the COVID vaccine is effective, and saved the day.

Here is a backgrounder I wrote on the subject of COVID vaccine fraud:

Making a vaccine look like it’s a champion isn’t difficult for public health agencies. There are a number of strategies.

Of course, these fraudulent strategies would be serious crimes. But when has that stopped the CDC or the World Health Organization?

In no particular order—-

ONE: Rework the definition of a “COVID case.” Presently, the CDC absurdly allows doctors to diagnose a person with COVID who has a cough, or chills and fever, and lives in an area where cases are being claimed. No test necessary.

So change this practice, once the vaccine is approved. Demand testing for a diagnosis. State that cough alone is not enough. Chills and fever must also be present. Require fever to be above 100.

These and other changes would automatically shrink the number of cases. The drop in numbers would be attributed to the vaccine.

This “definitional shrinking” was, in fact, deployed in the 1950s, after the introduction of the polio vaccine.

TWO: Order a change in the way the PCR diagnostic test is done. The practice of amplifying the original test sample from the patient occurs in cycles, or jumps. The greater the number of cycles, the more likely the test will result in a COVID diagnosis. Therefore, order a reduced number of cycles for all testing labs.

Outcome? Fewer COVID diagnoses. Fewer case numbers. “The vaccine is working.”

THREE: Quietly restrict the present hospital practice of arbitrarily writing “COVID” on patient case and death files.

FOUR: Cook up and publish false studies showing more and more people are developing immunity to the virus. Attribute this to the vaccine.

FIVE: Another type of false study—“the transmission of the virus from person to person is slowing, thanks to the vaccine.”

SIX: Pump up the success of issuing Immunity certificates after vaccination. “People are feeling safer now. More businesses are reopening…”

SEVEN: Using the compliant press, simply issue bald declarations that the vaccine is a success.

EIGHT: Hide the many instances of injury and death from the vaccine. When necessary, claim COVID was the cause.

NINE: Warn that the wonderful vaccine-derived immunity is not permanent, and frequent booster shots are necessary.

TEN: Rework the definition of “vaccine-acquired immunity.” Even a very weak antibody response from the shot would qualify as “protective immunity.”

ELEVEN: Huge numbers of people with ordinary flu-like illness, pneumonia, and other traditional lung infections are being called “COVID.” Change this practice. Go back to calling many of these people “flu,” “pneumonia,” etc. COVID case numbers will drop. Claim the drop is the effect of the vaccine.

TWELVE: Presently, millions of so-called COVID cases have “co-morbidities.” These are prior serious health conditions which are, in fact, the true causes of illnesses and death. Of course, this is denied. But after the vaccine is introduced… scale back the practice of counting all these ill and deceased co-morbid patients as “COVID.” Case and death numbers will drop. Claim the vaccine is the reason.

THIRTEEN: After the vaccine is introduced, slow down testing for a brief period. This will automatically reduce the rate of new cases. Attribute the decline to the vaccine.

Committing these crimes are a walk in the park for public health agencies.

And appointing official mouthpieces to carry lies to the public is as easy as training little Faucis to sit up and bark.

The Giant Virus in the Room: Corporate Vaccine Makers Need More Pandemics, to Grow

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By Dady Chery

Source: News Junkie Post

As drug makers prepare to make a killing on supposed vaccines against COVID-19, it is important, particularly for those who consider vaccines to be a wise investment today, or those whose retirement savings might get invested in such vaccines without their knowledge, to reflect on the fact that corporations are themselves viruses that can only make money for their investors by growing. The way they will grow is by making more vaccines for yet more pandemics. The new pandemics might come of their own accord, or they might get a little nudge.

A road map from those in the shadows

The public has lately been assaulted with relentless announcements about this or that supposed vaccine going into phase I or II clinical trial and the promise that vaccines — if we would only let enough different ones get developed sufficiently rapidly and without oversight — will free us from masks and social distancing. According to an American Enterprise Institute “road map” by people that include former FDA commissioners Scott Gottlieb and Mark McClellan, social distancing restrictions will only be lifted when tools to mitigate the risk of disease – including a vaccine — become available. There you have it. If you should ever want to stop cowering with a mask on your face, shake hands with a new acquaintance, dance with friends and strangers, blow a kiss or flirt more outrageously with somebody, you’ll need to get a vaccination license. The people who have mandated this aren’t even currently in government. They are private individuals who have retreated to think tanks from which to issue their decrees.

The global threat to health isn’t a coronavirus

The public health departments of cities, states, or countries have not been those to call for vaccines. Instead, global public health appears to have been hijacked by a supposed non-profit foundation called the Coalition for Epidemic Preparedness Innovation (CEPI), with the Orwellian motto, “New vaccines for a safer world.” One might well ask: “safer for whom?” CEPI was hatched in a one-hour discussion on the sidelines of Davos 2016 between Bill Gates, Wellcome Trust Foundation Director Jeremy Farrar, the CEOs of six major vaccine manufacturers (Glaxo Smith Kline, Merck, Johnson & Johnson, Sanofi, Takeda, and Pfizer), the Prime Minister of Norway, and supposedly 15 other individuals.

Representatives of Germany, India, and Japan are supposed to have attended that meeting, although Prime Minister Angela Merkel had declined the invitation that year, Indian Prime Minister Narendra Modi was not there, nor was any Japanese head of state. The goal of this cabal, in which elected heads of states are obviously subordinate to Bill Gates and Big Pharma, is not merely to make vaccines and lots of money, but also to deregulate vaccine manufacture on a global scale and control the world by controlling global public health. In this scenario, the United Nations’ WHO, which receives 75 percent of its funds from big pharmaceutical companies and the Bill & Melinda Gates Foundation, is merely the arm of CEPI that will tie vaccine adoption by developing countries to various kinds of Western aid. The WHO Director General, Tedros Adhanon, began to enjoy the Gates Foundation’s generosity when he was a Minister of Health in Ethiopia who embraced the foundation’s agenda. The WHO Assistant Director General, Bruce Aylward, who may be the real power in the organization, previously worked for Gates’ supposed polio eradication program. Make no mistake: CEPI intends to be to global health what the WTO is to global trade.

The agenda is military, and it is global

CEPI has already raised over $750 M: a sum that commands a lot of influence. It is well entwined with the militaries of various countries. For example CEPI’s CEO, Richard Hatchett, was the Director for Biodefense Policy on the White House Homeland Security Council in 2005-2006, Associate Director for Radiation Countermeasures Research and Emergency Preparedness at NIAID in 2005-2011; and Chief Medical Officer and Deputy Director of the Biomedical Advanced Research and Development Authority (BARDA) in 2011-2016. BARDA is a division of the Office of the Assistant Secretary for Preparedness and Response. Several CEPI-financed vaccine projects enjoy support from BARDA, the U.S. Department of Defense Advanced Research Projects Agency (DARPA), or the U.S. Military HIV Research Program.

In January 2020, CEPI announced that it would finance three consortiums to develop vaccines against COVID-19. Its alliance with these consortiums, however, predates this announcement in several cases. For example, as far back as April 2018, CEPI provided $56 M to a company called Inovio to get vaccine candidates against the SARS-Cov-2 relative, MERS-CoV, to Phase II trials; Inovio’s main collaborator is the Chinese company, Beijing Advaccine Technology. In January 2019, CEPI provided $10.6 M to a consortium involving the University of Queensland and public/private sector partners in Australia, the US, and Asia to develop a new approach called “molecular clamp” for designing vaccines. In Dec 2019, CEPI gave $8.4 M to Imperial College London, UK, to test an RNA vaccine in animals and also get it to Phase II trials. The researchers at Imperial College boast about the fact that they began to test their vaccine against SARS-CoV-2 in animals in February 2020! Recall that the SARS-CoV-2 genome sequence only became known on January 10, 2020. In this context, it is also interesting that Imperial College is the home of the fear mongering and disgraced Neil Ferguson, with the too pretty and too married social merging mistress.

The FDA’s vaccine fast track

The road to FDA approval has been smoothed for CEPI’s partners and, unsurprisingly, they have been first to move their putative vaccines to clinical trials. As a rule, the FDA has put the projects of CEPI’s pet companies on a “fast-track” designation, which allows them to be green-lighted to the next phase before they have even completed the preceding one. Consider for example the biotechnology company, Moderna. It has received an undefined sum from CEPI, plus around $483 M from BARDA, as well as funds from DARPA. The appeal of this company to pencil and paper want-to-be-scientists, like Bill Gates and various military types, is that its approach, or “platform,” for vaccine manufacturing could potentially be used to make many other vaccines. But this approach is also potentially dangerous, because it involves the introduction of viral mRNA into cells, and this alone might start an adverse immune reaction. The viral mRNA is then supposed to direct production of the SARS-CoV-2 spike protein on the surface of the vaccinated person’s cells for some undefined period of time. This kind of vaccine was not even tested in animals before Moderna was allowed to begin its phase I trial in mid-March with 45 healthy human volunteers. Even more extraordinary, six weeks later the company filed for permission to go on to a phase II trial with 600 volunteers. Its application was approved, even though the phase I trial requires months of follow up that are not yet done. The company’s stock has skyrocketed as it has made one promise after another of accelerated schedules and massive scale up of its vaccine production.

Inovio is on a similar trajectory. The phase I trials on its putative SARS-CoV-2 vaccine started on April 3. The company is injecting people with milligram amounts of DNA and then zapping them with a proprietary device, to get the DNA into their cells. It has not defined how the DNA carrying the spike protein information will be guided to the nucleus. If the DNA stays elsewhere in the cells, where it does not belong, it might be mistaken for a virus and start an adverse immune response. If it goes to the nucleus, it may integrate into the cells’ DNA in random places, potentially causing cancers.

The mainstream takes dictation

The mainstream media, which is as lazy as it is scientifically illiterate, has contented itself with the republication of gee-whiz, oh-wow press releases, and the publication of reports sometimes explicitly written by the vaccine manufacturers or their partner foundations. Such reports also appear, not as full-length peer-reviewed articles, but as short commentaries in the summary and editorial pages of serious science journals like Science and Nature. The association of those planted reports with prestigious journals gives them, not only a veneer of credibility but also an automatic amplification by popular science magazines. The reports have generally focused on the marvelous promise of the supposed vaccines and their inevitable manufacture in massive quantities. In fact, 18 years after the original SARS-CoV, which is the closest relative of the COVID-19 agent, no vaccine has successfully been developed against that virus, and many of these so-called new vaccine efforts are actually recycled failed SARS-CoV or MERS-CoV projects.

The real state of knowledge about the immune system

What the news media do not say, and probably could not say with any confidence, is that the mammalian immune system is still poorly understood. Had most media people attended a BIO101 class, there would be great skepticism in the news about the sudden proliferation of newfangled vaccines and the massive human experiment being organized to test them.

The following is a quote from a scholarly review published in Nature Immunology in December 2014:

“The only currently licensed and generally available vaccines against respiratory viruses are for influenza virus, and even these are suboptimal. The paucity of vaccines is due in part to the only limited understanding of immune responses that can provide protection against respiratory viral infection: in many cases, even fundamental correlates of protection have yet to be accurately defined, and the most appropriate antigens to which vaccines should be targeted remain unknown. Animal models are generally imperfect guides to human disease, and the populations at highest risk of severe infections (i.e., young children and elderly adults) are the most difficult to study. In addition, vaccines are often less effective in those with immature or senescent immune systems.”

The next quote is from a commentary on a peer-reviewed article published on May 13, 2020 in Nature 581: 316.

“This discovery elevates TASL to membership of an exclusive circle of… adaptor proteins… of which the other members are TRIF, MAVS, and STING. These four proteins together control the type I interferon response induced by nucleic-acid sensing, a picture that has now been completed with the discovery of TASL as the missing… adaptor of TLR7, TLR8 and TLR9 signaling.”

My translation: only this week, one of the four major players in the early human immune response was discovered! It is a newly characterized protein called TASL that becomes activated when an infected cell senses the presence of genetic material from a virus in a cellular compartment where it should not be. This helps to explain an important part of the immune response that until now has baffled scientists.

The early fight against an infection: a situation that can escalate

A reasonable analogy to a viral infection might be a Columbine-like threat, where a band of murderous fascists take over a high school. Let us say, for good measure, that this particular group wears a specific and recognizable kind of uniform and tattoo. The high school itself is automatically set up to detect the invasion and to call 911. Cells in the lung do the equivalent with proteins called Toll Like Receptors (TLR). These proteins sound the alarm when they recognize genetic material, like DNA or viral RNA, in compartments outside of the nucleus, where it is not supposed to be: a situation that indicates presence of a pathogen. In the cells, some of these compartments are called endosomes or endolysosomes. In our high school, the first responders would be the local police. In the lungs, which do contain their own local immune cells, this would be called the interferon or antiviral response. If this response is successful, as it often is in healthy people, nothing more needs to be done: end of story.

But suppose some of the fascists manage to evade the police and take over several other schools in the same area. The police might then call in SWAT teams with snipers, machine guns, and tear gas grenades; or even police units with bomb robots. The innate, or local, immune system has the equivalent of all of these. It involves SOS signals to the adaptor proteins noted in the above quotation, and the permission from each one for the next step in the escalation. The bomb robots in this case, would be analogous to an inflammation response that destroys not only the viruses but also much of the lung. Obviously, you would want to exhaust every option before using bomb robots in schools that have a few crazies and a lot of students. But suppose the crazies manage to block the police communication to the SWAT teams, then what do you do? Coronaviruses, including the agent of COVID-19, i.e. SARS-CoV-2, can achieve an analogous block of communication during exceptionally heavy initial infections, or infections of the elderly and people with other medical conditions like diabetes, respiratory problems, or cardiovascular disease. What I have just described, with a minimum of immunology jargon, is called the initial innate immune response. In this context, innate means local, i.e. in the lungs.

Vaccines are not the answer

The serum antibodies we all know about are produced as part of a later response, called the adaptive immune response. It happens in those who manage to keep intact and functional a sophisticated route of communication during the attack. The resulting counterattack is not only broad but also specifically tailored to neutralize the invading virus. Furthermore, we maintain a memory of the response. This would be the equivalent of an FBI database with detailed descriptions of the crazies and their tattoos so that they might immediately be recognized, should they appear again in months to years. The only problem is: they can change uniforms and tattoos. All vaccines are based on inducing this later response, which is supposed to prime an individual to resist an attack. But vaccines, however sophisticated the supposed approach or platform, are almost always designed to recognize only a single feature of the invading pathogen. As if one learns to recognize a tattoo on a fascist and nothing more. But suppose the tattoo is removed or changed? In the case of SARS-CoV-2, the target is the spike protein, or sometimes a piece of it. It so happens that the spike protein is also the most variable part of the virus.

Antibody-Dependent Enhancement of disease: A bon entendeur, salut!

A massive human experiment is underway to test potential vaccines. Nearly everything that can be put into a human will be injected into those volunteers who are more terrified of COVID-19 than the vaccine makers or the military. Their menu will include: the inactivated SARS-CoV-2; mutated, or attenuated, versions of SARS-CoV-2 (intra-nasally); SARS-CoV-2’s spike protein; pieces of the spike protein, large and small; harmless bacteria that have been redesigned to make the spike protein; harmless viruses that have been redesigned to make the spike protein; virus-like particles that can present the spike protein on their surface; circular DNA that codes for the spike protein; linear DNA that codes for the spike protein or part of it; mRNA that codes for the spike protein; modified mRNAs; and even an RNA that codes for the spike protein as well as another protein that will make more of the RNA and spike protein, ad infinitum. As a rule, the manufacturers have not even disclosed which exact version of the spike protein they plan to use for the vaccination attempts. Indeed, some companies have disclosed nothing but their intent to conduct clinical trials.

One possible result of attempted vaccinations against SARS-CoV-2 that should give anyone pause is an Antibody-Dependent Enhancement (ADE) of disease. In other words, it is possible that attempted vaccinations might prime a previously healthy person for a life-threatening inflammation response on the next encounter with a coronavirus. So far, the only company that reports even having checked for ADE is Sinovac Biotech, a Chinese company that is collaborating with a US partner on an inactivated SARS-CoV-2 vaccine. The phenomenon of ADE is well established as a possible outcome of attempted vaccination against viruses. A famous instance was a late 1960s vaccine trial in children using inactivated Respiratory Syncytial Virus (RSV), which resulted, not only in a failure to protect but also in 2 deaths, and a severe respiratory disease in 80 percent of the children that required hospitalization on their subsequent exposure to the virus. ADE has been observed in mice and other animals supposedly immunized against SARS-CoV with an inactivated virus. Recall that SARS-CoV is the closest relative of SARS-CoV-2. Therefore, compared to the supposedly vaccinated people, it is highly possible that the unvaccinated or never previously exposed individuals will fare better in a subsequent coronavirus outbreak.

Hydroxychloroquine bites back

The new adaptor protein, called TASL, described for the first time this week, was discovered to bind to another protein called Solute Carrier 15A4 (SLC15A4). SLC15A4 has long been known to be necessary for lupus and other autoimmune diseases. Now we know that the reason for this is probably because the TASL-SLC15A4 interaction is the path that leads to inflammation. Remember the robot-bomb option in the previous section? That’s the one! As it happens, the reason hydroxychoroquine (HC) has worked for decades against lupus disease is because HC is known to interfere with inflammation, but the details were unknown. SLC15A4 is also important for maintaining the acidity of the endosome, which HC is known to de-acidify to some degree. The antibiotic azithromycin has also been reported to reduce the acidity of endosomes, thus compounding this effect of HC. As a result, when the virus goes to the endosome to develop, it finds that this compartment is insufficiently acidic; it gets stuck there and is ultimately destroyed. So hydroxychloroquine, an inexpensive and long-used drug, counters coronavirus infections in two crucial and quite general ways: it damages the virus and also keeps the immune response from going dangerously overboard. Given the connection of SLC15A4 to lupus disease, it is astonishing that the authors of the new paper did not test HC’s effect on their system containing TASL. But much is open to revision when one wants to publish in Nature. That piece of the puzzle will surely materialize. But timing is everything, and it’s no wonder that the vaccine makers are in such a rush.

For the record

The biggest populations of human subjects for vaccine trials have in the past been brown and black children from countries like India, Bangladesh, Vietnam, Mexico, and Haiti. The scale of the current project is so massive, however, that even the citizens of Western countries must be preyed upon. In this regard, it certainly helps to keep everyone terrified. The biggest market for vaccines used to be the US Army, but that may change. Besides, a cowed and sick general public should be far more manageable, as climate change events exacerbate stressors like displacement and hunger. The greater the number of epidemics and vaccine-associated diseases, the greater the boon will be for pharmaceutical companies, and the faster they will grow. I write for the record. Those of you who participate in this enterprise or invest in it can no longer say that you did not know what was being done. The rest of you on the sidelines can still change this dystopian future, but the window of opportunity is narrowing fast.

Editor’s Notes: Dr. Dady Chery is an Associate Professor of Biology, Co-Editor-In-Chief of News Junkie Post, and the author of We Have Dared to Be Free: Haiti’s Struggle Against Occupation.  

 

A New World Is Being Born: What Will It Be?

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By Paul Craig Roberts

Source: PaulCraigRoberts.org

We are hearing from many that the world after Covid-19 will be different.  The question is:  Different in what way?  Will it be better or worse?

Elites are working to make it better for them, and worse for the rest of us.  About that the evidence is clear.  The Big Boys are being bailed out and their debts covered.  Everyone else, except those already marginalized and without a recent work record and fixed address, got a month’s rent and extended unemployment benefits.

Big Pharma sees massive profits in the virus, Government sees more power to control

But the disparity in economic benefits is only a part of it.  Powerful vested interests, such as Bill Gates and Big Pharma, are determined to vaccinate us all, and to control our movements with an internal passport called “vaccinated, health cleared” or other words to that effect.  New tracking procedures and technologies are to be put in operation reminiscent of the “mark of the beast” to police the access of varous categories of people to various areas and benefits.

Experts point out that just as we cannot be vaccinated against the common cold, except perhaps for the past year’s version we cannot be vaccinated against Covid-19 and other mutating viruses, but the experts are already being shouted down. No expert opinion is to be permitted to stand in the way of vaccination profits.

Neither will nutrition and vitamin advocates be allowed to get in the way.  Bill Sardi predicts that orchestrated scares generated by mandatory recalls of “toxic” vitamins await us ( https://knowledgeofhealth.com/modern-medicine-laid-bare/ ). Big Pharma is determined to acquire control over vitamins and homeopathic remedies, and the FDA is Big Pharma’s likely pawn.

Vaccination has been elevated above cure, as Big Pharma and its shills such as CNN shout down the positive experience doctors report of successful treatments with Hydroxychloroquine and Azithromycin, and the effectiveness of Vitamin C, Vitamin D3, and Zinc in strengthening the ability of immune systems to fight off the virus.  Big Pharma-influenced medical orthodoxy cannot get out of the box it has been put into.  When new thinking and experimentation are needed, those capable of thought are hasseled and even blocked by FDA regulations and dogmatism.

The permanent government and its security agencies see in the population’s fear and confusion opportunities to put into place more tyrannical measures, more set-asides of Constitutional Rights, more impairments on free speech.  The ability of freedom to resist oppression is ever diminished.

Various descriptions of the expected dystopia are offered on the Internet.  But it does not have to turn out this way.  It is up to us. Demoralized and fearful, we can accept more government power as we did after 9/11.  Instead, we can collectively recognize the massive failure everywhere of Western leadership and construct a more liveable and sustainable society.

The failure of leadership is an opportunity for real change

CNN, the New York Times, and the rest of the controlled media tell us every day that President Trump represents the failure of leadership.  But the failure of leadership goes beyond all the leaders of the last 30 years and resides in the system itself.  Global, “self-regulating,” greed-driven, financialized, soulless capitalism cannot unite people into a sustainable community.

The failure of leadership resides in the long-term failure of leadership that made Western societies vulnerable by moving high-productivity, high-valued jobs offshore in order to raise corporate profits at the expense of domestic consumer incomes.  It means the movement offshore of the ability to produce medicines, N95 masks, and other needed resources for national survival.  It means dependency on foreign powers.  It means the inability to function without massive imports.  However you look at it, globalism is a death sentence.  Its only advantage is to the rich, and the advantage comes to them in the form of cheap labor that swells their profits while it shrinks domestic incomes and the purchasing power of the population.

Without incomes to drive the economy, the elites provided loans and expanded credit in order to provide spending power based in personal debt to absorb the offshored production brought home to sell in American markets. The cost of college education soared as its quality declined.  Education subsidies were cut and student debt substituted in its place.  Inflation was understated in order to deny Social Security pensioners cost-of-living increases. Medicare payments to health care providers were squeezed down.  The social safety net was ripped again and again. More and more people fell out, and homeless populations grew providing fertile breeding grounds for Covid-19.

The income and wealth distribution in the US went from fair to extremely unequal in a short time as the rich profited from the Federal Reserve pumping trillions of dollars into the prices of financial assets and from corporations buying back their own stock, thus decapitalizing the corporation while taking the company into debt, all for the temporary benefit of higher bonuses for executives and more capital gains for shareholders.  The elites killed the economy for short-run benefits to themselves.

These destructive polices were the work of greed-driven short-term thinkers—people whose only vision was “I want even more.”  And it is these unworthy people, not their victims, that Uncle Sam is now rescuing.  The massive unpayable debt bubble that already overhung the economy is being blown larger.  The Federal Reserve and the US Treasury are in the process of destroying the US dollar in futile efforts to save the super-rich from their own greed-driven misbehavior.

In place of this insane approach to the economic crisis, there is a sane approach.  The bailed out corporations and banks are in effect being purchased by the government.  Therefore, they should be treated as the nationalized corporations that they are.  Once nationalized, the government, unlike the corporations, can create the money to pay the salaries and health premiums. The predicted 30 or 40 percent unemployment can be avoided.  It is better to pay salaries than to pay unemployment benefits.  The psychological difference alone is worth a vast amount.

The inability of the high-cost American private health care system to cope with the present medical crisis is apparent.  A profit-driven health care system is the highest cost system to have.

Profit is built in at every level, which raises costs to levels that private insurance and Medicare refuse to reimburse.  The result is shrinkage, not expansion of the system.  Just look, for example, at the number of hospitals, especially in rural areas, that have recently closed.

Moreover, the coverage of a private system—and Medicare itself—has massive gaps.  The resistance to a nationalized health service is ridiculous, especially as a nationalized service can coexist with a privatized one.  Two are clearly better than one.

Nationalization has numerous benefits.  It permits the large unwieldly enterprises, created, for example, by the mergers of giant banks like Chase Manhattan and J.P. Morgan, to be broken up and to reestablish the separation of commercial from investment banking.  The repeal of the Glass-Steagall Act and the suspension of enforcement of the anti-trust laws were ignorant policymaking at its worse. Nationalization permits the government to bring home the offshored production of global US corporations and to put the US workforce back to work in middle class jobs.  It is win-win for the American people.

Once the giant monopoly corporations are broken up, they can be privatized and returned to private ownership on a fair value basis, not on the giveaway basis of a pennies on the dollar sale. The money the government receives from their sale can be used to retire government debt.

For individuals, the life- and economy-suffocating heavy debts should be written down to levels that can be serviced by their incomes.  Michael Hudson and I proposed a “debt jubilee” as a solution:  https://www.paulcraigroberts.org/2020/03/25/a-brady-bond-solution-for-americas-unpayable-corporate-debt/   Others have taken up our call:  https://truthout.org/articles/1200-only-goes-so-far-its-time-to-abolish-debt/?eType=EmailBlastContent&eId=98cb6aac-8ef8-4e0e-b80e-24a1d1f92ef6

Currently the Federal Reserve is socializing debt without writing it down.  This is nonsensical as it bails out debt by expanding it. 

In the US there is so much dogmatic prejudice against anything that has a tint of socialism, even as a temporary expedient measure, that thought and sensible action face strong barriers.  If we cannot overcome these barriers, we are destined for far more difficult times.

Can community be restored or will nationality degenerate into the clans and tribalism of Identity Politics?

The greatest challenge we face is to restore the concept of community.  There was a time when  the United States was a community, a unique one as it consisted of a multitude of ethnicities. As each wave of ethnic immigrants arrived, they passed a test on the Constitution, learned the national language, and became assimilated into the American community.

This community has been destroyed by a variety of forces, the latest being Identity Politics.  Identity Politics prohibits community by breaking down the population into mutually hostile groups by gender, sexual preference, race, and whatever classification can be invented or imagined.  The result is a Tower of Babel.  A Tower of Babel is not a community.

Instead of community, the US is a place where hatreds are cultivated with those claiming the status of victims doing the most hating and those assigned the status of victimizer being most hated.  Initially, white hetereosexual males were the primary hate objects, but lately we have the transgendered hating the feminists who say that a woman is a woman, not a man who claims to be a woman.  The transgendered attacks on well-known feminist leaders are violent in their language and are likely to progress into violent deeds.  Various unassimilated immigrant groups battle each other over who controls disputed territory.  Israel’s inhumane treatment of Palestinians has enraged Muslim immigrants against Jews.  Violent racial attacks on white people are becoming more common.

For decades Women’s Studies have taught hatred of men, and Black Studies have taught hatred of Whites.  This taught hatred is now supplemented by the New York Times 1619 Project.  In place of assimilation, we now have mutual hatreds.  How do we escape from this?

Perhaps the challenge from Covid-19 will force us to come together again in order to prevail over the virus, which in mutated versions might be with us forever.  A coming together would be helped by an economic bailout perceived as fair rather than as the one-sided approach that has been taken. A debt jubilee provides the necessary fairness.

The elites by thinking only of their interests are in the way of the opportunity that crisis provides to bring people together.  If we can’t be brought back together, we can forget about unity beyond the boundaries of our own victim or identity group.  In place of community, we will be organized in clans of seperate identities.  The absence of unity at home will make us a sitting duck for enemies abroad.

We know what the Dystopian Wish List is.  Can we come together with an anti-dystopian wish list as a mutually supportive community or have the elites succeeded in atomizing us into disparate tribal hate groups?

RFK Jr. Slams Gov’t & Big Pharma In Eye Opening Speech About Forced Vaccinations

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By Arjun Walla

Source: Collective Evolution

California has very strict compulsory vaccination laws for children in school, and as a result more parents are deciding to homeschool their children. The latest information regarding vaccines in California that’s making noise is Senate Bill 276 by Senator Richard Pan. The bill eliminated nearly all vaccine medical exemptions. Under this bill, politicians, not physicians, are in charge of deciding whether or not children may receive medical exemptions, which in turn would determine whether or not they can attend school.

This bill, which was recently signed into law, represents medical tyranny that is similar to a police state. Forcing vaccinations on any segment of the population and taking away their freedom of choice is ridiculous. All of this is done under the assumption that unvaccinated children pose a danger to vaccinated children, and this is simply not true for several reasons.

Herd immunity is a largely theoretical concept, yet for decades, it has furnished one of the key underpinnings for vaccine mandates in the United States. The public health establishment borrowed the herd immunity concept from pre-vaccine observations of natural disease outbreaks. Then, without any apparent supporting science, officials applied the concept to vaccination, using it not only to justify mass vaccination but to guilt-trip anyone objecting to the nation’s increasingly onerous vaccine mandates.

In a 2014 analysis in the Oregon Law Review by New York University (NYU) legal scholars Mary Holland and Chase E. Zachary (who also has a Princeton-conferred doctorate in chemistry), the authors show that 60 years of compulsory vaccine policies “have not attained herd immunity for any childhood disease.” It is time, they suggest, to cast aside coercion in favor of voluntary choice.

This is true, in fact, there has been a history of disease outbreaks in heavily vaccinated populations. I wrote an article not long ago providing multiple studies showing this, and the studies are elaborated on and linked in that article, which you can go through here.

According to a MedAlerts search of the FDA Vaccine Adverse Event Reporting System (VAERS) database as of 2/5/19, the cumulative raw count of adverse events from measles, mumps, and rubella vaccines alone was: 93,929 adverse events, 1,810 disabilities, 6,902 hospitalizations, and 463 deaths. What is even more disturbing about these numbers is that VAERS is a voluntary and passive reporting system that has been found to only capture 1% of adverse events.

How can vaccines produce herd immunity if they’re not safe for everybody? It’s impossible.

The various forms of vaccine failure not only make herd immunity impossible to achieve, but also feed the occurrence of “vaccine-preventable illnesses” in highly or even fully vaccinated populations. There are numerous examples of this in published literature, again, some of which I link and go into greater detail about measles here.

Vaccines Aren’t Safe For Everyone

It’s no secret that vaccines are not completely safe for everyone, it’s clearly not a ‘one size fits all’ product, and that’s evident by the fact that nearly $4 billion has been paid out to families of vaccine injured children via the National Childhood Vaccine Injury Act (NCVIA). As astronomical as the monetary awards are, they’re even more alarming when you consider that only an estimated 1% of vaccine injuries are even reported to the Vaccine Adverse Events Reporting System (VAERS). If the numbers from VAERS are correct – only 1% of vaccine injuries are reported and only 1/3 of the petitions are compensated – then up to 99% of vaccine injuries go unreported and the families of the vast majority of people injured by vaccines are picking up the costs, once again, for vaccine makers’ flawed products.

This completely debunks the validity of herd immunity.

Speech From Kennedy

While California’s tragic fall into what might rightly be described as a Medical Police State has many up in arms, RFK Jr. spontaneously delivered a speech outside Gov. Newsom’s office, helping to transform the anger and grief experienced by thousands of shaken onlookers into inspiration and hope, no doubt catalyzing further what is clearly becoming this country’s next grassroots civil rights movement.

In the astoundingly powerful and uplifting speech by RFK Jr. below, one senses the historical importance of what just transpired. And that the fall of California into medical fascism also marks the beginning of a new, broad-based civil rights movement, including all sexes, races, walks of life, religions, and socioeconomic classes — as it concerns the primary, inviolable human right of bodily self-sovereignty and health freedom, and a parent’s right to make informed health choices for their children, which can have life and death consequences. [From the Youtube video description]

https://www.youtube.com/watch?v=jPn86xIjpq0&feature=youtu.be

Another Informative Statement From Kennedy

Via Robert F. Kennedy Jr.

Merck introduced its measles vaccine in 1963, claiming the vaccine would convey lifelong immunity equivalent to a natural infection, with health officials promising that 55% vaccine coverage would produce “herd immunity” sufficient to eradicate measles by 1967.

Leading scientists of the day, including the world’s preeminent bacteriologist, Sir Graham Wilsonand Harvard Virologist John Enders, who first isolated measles, warned against introducing a vaccine unless it provided lifelong immunity. Measles, they cautioned, would rebound with increased virulence and mortality as the vaccine forced the evolution of more virulent strains and shifted outbreaks away from children—biologically evolved to handle measles—to the elderly who could die from pneumonia, and young infants now unequipped with maternal immunity.

A 1984 Johns Hopkins University modeling study predicted that Merck’s population-wide experiment would increase measles outbreaks by 2050, (when the last generation subject to natural immunity died off,) compared to the pre-vaccine era. This is exactly what has happened. Merck’s vaccine, with a growing failure rate has been incapable of abolishing the disease. Vaccine failure has left millions of adult Californians effectively unvaccinated. And 79% of people affected by measles in this year’s California outbreak were adults.

When eradication predictably didn’t materialize and measles attacked fully-vaccinated populations, Merck simply moved the goalpost saying that herd immunity required 75% vaccination, then 85%, then 95%, then 98%. And now 99%. To distract the world’s citizens from its failed vaccine, Merck started blaming “anti-vaxxers.” (The Vaccine Safety Movement)

California’s bought or brain-dead lawmakers are proposing to “fix” Merck’s vaccine failure problem by punishing 4,000 vulnerable children with medical exemptions. In an act of legislative savagery, Democratic politicians propose to forcibly vaccinate children whose doctors have told them that a vaccine could kill or severely injure them. SB276 will not fix the measles outbreak or solve the problem of vaccine failure, it will only reward a corrupt company for a defective product.

The Takeaway

The idea that politicians can force children to be vaccinated, including those deemed to be in danger of severe adverse reactions, and strip them of their rights to attend public school is insane. Freedom of choice and medical freedom should always exist, especially with regards to vaccines. If parents want to vaccinate, fine, but parents who wish to not vaccinate their children for whatever reasons should always have the freedom to do so.

Mandatory vaccination is tyrannical.

“The fight for liberty and health freedom in California is far from over. There will be legal challenges,” said RFK. Jr., “all the way up to the Supreme Court if necessary. In fact, this incident brings to the forefront a deep, dark problem in the United States that has been festering for decades: the rise of the Pharmaceutical industry’s influence on the government to mandate products that the free market would otherwise reject, due to the profound liability these products have now underwritten completely by the government via their indemnification through the National Childhood Vaccine Injury Compensation Act (NCVIA) of 1986. Now, over three decades since the inception of NVICA, that same industry is starting to use the police powers of the state to enforce these mandates.” [Taken from the Youtube description in the video posted above]

Harvest of Greed – the Merger of Bayer and Monsanto

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By Dr. Mercola

Source: Waking Times

The featured documentary, “Harvest of Greed,” investigates a number of the many issues brought about by the merger of Monsanto and Bayer AG. The merger was initially announced in May 2016, when Monsanto accepted Bayer’s $66 billion takeover offer — the largest all-cash buyout on record.1,2,3

The U.S. Department of Justice (DOJ) approved the merger in April this year,4 following the European Union’s (EU) approval in March. As a condition of the DOJ’s approval, Bayer will sell some of its assets to BASF — its German competitor — before the finalization of the merger.

This includes its soybean, cottonseed and glufosinate weed killer businesses, which overlap with Monsanto’s and were antitrust sticking points. Combined, Bayer and Monsanto used to control nearly 60 percent of the American cottonseed market. Monsanto also owns the rights to 80 percent of corn and 90 percent of soybeans grown in the U.S.5 The EU also demanded Bayer eliminate about $7.4 billion-worth of its various firms “to ensure fair competition.”6

Mega-Entity Now Controls Large Portion of Global Seed Supply

This new entity is now the largest seed and pesticide company in the world, controlling more than 25 percent of the global seed and pesticide supply. In all, just three companies now dominate the global seed and pesticide market.7 (In addition to the Bayer-Monsanto merger, the DOJ has also given the Dow-DuPont merger the green light, and the Federal Trade Commission recently approved ChemChina’s acquisition of Syngenta.)

The Bayer-Monsanto merger generated deep concerns right from the start, and anti-competition regulators were urged to investigate the takeover. Bernie Sanders went on record saying the takeover poses “a threat to all Americans” and needed to be blocked.8 He also urged the DOJ to “reopen its investigation of Monsanto’s monopoly over the seed and chemical market.” Farmers have also expressed concern over what the merger might do to prices, as less competition inevitably tends to lead to price hikes.

As just one example, the price of a bag of seed corn has risen from $80 to $300 over the past decade alone — a price hike attributed to the consolidation of seed companies and reduced competition. The merger of Bayer and Monsanto is predicted to make matters worse. Farmers also worry that consolidation will result in lower quality products by reducing incentive for innovation. Organic farmers have their concerns as well. As noted by Food and Power:9

“For Kristina Hubbard, director of advocacy and communications for the Organic Seed Alliance, the merger presents a particular threat to organic farmers. She notes that the National Organic Program’s regulations on organic seeds generally dictate that growers must use organic seeds to grow their crops. But there is an exception granted for non-organic seed when ‘an equivalent organically produced variety is not commercially available.’

Acceptable non-organic seeds are generally owned by the giant seed companies. ‘That exemption is important because currently the supply [of organic seeds] isn’t sufficient to meet the diverse and regional needs of all organic farmers,’ she says. With continued consolidation in the seed industry, she says farmers that rely on those non-organic seed options may find themselves faced with even fewer options as the merged companies cut down on research and development.”

Bayer-Monsanto Merger Unlikely to Benefit Anyone but Its Shareholders

Bayer AG’s CEO, Werner Baumann, has stated that “it is not our plan or our ambition or our intent to prevent farmers from having choice.”10 But the history of Monsanto and Bayer both suggest it would be naïve to believe him. As noted by Mark Connelly, an agriculture analyst at the investment group CLSA Americas, “These companies want to make more money, they want to raise prices. No company in this industry needs these deals in order to innovate.”11

Indeed, there can be little doubt that the Bayer-Monsanto merger will give the subsequent entity even more power to bully farmers into paying more and pressuring and manipulating governments into accepting the unacceptable risks posed by genetically engineered (GE) crops and mounting use of ever more toxic pesticides.

One example of Monsanto’s strong-arm tactics included in the film is that of India, where more than 300,000 farmers have committed suicide due to farm-related debt. When the government attempted to regulate the price of seed — the main cause leading to these debts — Monsanto sued the Indian government.

Between 1997 and 2014, Monsanto also sued 147 farmers for “improperly reusing patented seeds.”12 They never lost a single case, even in cases where organic fields were contaminated or cross-pollinated with unwanted GE seeds.

Billions Against Bayer

In response to the announcement of the merger in 2016, the Organic Consumers Association (OCA) launched a boycott against Bayer. The “Billions Against Bayer” campaign is essentially a continuation of the successful “Millions Against Monsanto” campaign. Following the DOJ’s April approval of the merger, OCA renewed its call for consumers around the world to join the boycott. You can follow the campaign and get the latest news updates on Facebook.13 As noted in a September 2016 press release:14

“Two of the world’s most foul corporate criminals will be one. Monsanto will pack up its headquarters and head overseas. The much-maligned Monsanto name will be retired. But a corporate criminal by any other name — or size — is still a corporate criminal.

This merger only heightens the urgency, and strengthens our resolve, to hunt down the corporations that are poisoning everything in sight. We will follow them to the ends of the earth, if need be. We will expose their crimes. We will end the toxic tyranny. We will become the Billions Against Bayer. And we will need your help …”

Even many Bayer employees are leery of the merger. While both companies have checkered pasts, Bayer has managed to escape the brunt of the kind of criticism, if not hatred, leveled at Monsanto over the years.

According to the featured documentary, Bayer claims the merger has widespread support among its staff, yet when Bayer employees were approached under the promise of anonymity, the general consensus was one of dismay at inheriting Monsanto’s tarnished reputation. Such fears are likely to come true sooner rather than later. Activists in Argentina, for example, promise Monsanto’s ill reputation cannot be washed clean but will now transfer over to Bayer.

Glyphosate — A Toxic Legacy

Both Bayer and Monsanto insist that glyphosate, the active ingredient in Monsanto’s weed killer Roundup and other herbicide formulations, is “a very safe product when used properly.” In the video, Bayer CEO Werner Baumann stresses that more than 3,000 studies support the chemical’s safety. Yet numerous studies have reached the converse conclusion, showing it poses toxic risks to soil, animals and humans.

“The things you hear in the public debate are ultimately based on misinformation about the risks of this product,” Baumann says. “So, we think glyphosate, even if it does belong to our company, is a good product, and its license should be renewed.”

At the end of 2017, the EU did indeed renew its approval of glyphosate for the next five years,15 but the process was not without its critics, such as Martin Häusling, member of the Green Party and the European Parliament, who noted that many of the studies exonerating glyphosate were funded by Monsanto itself, while independent research keeps finding problems.

Indeed, scientists have discovered it not only may be carcinogenic,16 but may also affect your body’s ability to produce fully functioning proteins, inhibit the shikimate pathway (found in gut bacteria) and interfere with the function of cytochrome P450 enzymes (required for activation of vitamin D and the creation of nitric oxide and cholesterol sulfate).

Glyphosate also chelates important minerals, disrupts sulfate synthesis and transport, interferes with the synthesis of aromatic amino acids and methionine, resulting in folate and neurotransmitter shortages, disrupts your microbiome by acting as an antibiotic, impairs methylation pathways, and inhibits pituitary release of thyroid stimulating hormone, which can lead to hypothyroidism.

Recent Government Tests Show Roundup Is More Toxic Than Glyphosate in Isolation

Most recently, toxicology testing17 by the U.S. National Toxicology Program (NTP) concluded the Roundup formula is actually far more toxic than glyphosate alone.18 The NTP testing was done by request from the U.S. Environmental Protection Agency (EPA) following the International Agency for Research on Cancer (IARC) reclassification of glyphosate as a Class 2A probable carcinogen three years ago.19

At the time, the IARC noted concerns about glyphosate formulations possibly having increased toxicity due to synergistic interactions. As it turns out, that’s exactly what the NTP testing found. According to the NTP’s summary of the results, glyphosate formulations “significantly altered” the viability of human cells by disrupting the functionality of cell membranes.

Mike DeVito, acting chief of the NTP Laboratory commented on the results saying, “We see the formulations are much more toxic. The formulations were killing the cells. The glyphosate really didn’t do it.”

Internal documents from Monsanto, obtained through previous Freedom of Information Act (FOIA) requests, reveal Monsanto’s own employees have not been convinced the product is harmless either. For example, in a 2002 email, Monsanto executive William Heydens said, “Glyphosate is OK but the formulated product … does the damage.”20

Monsanto Charged With Crimes Against Humanity

October 16, 2016 (on World Food Day), Monsanto was put on trial for “crimes against nature and humanity” at a tribunal in The Hague, Netherlands. The steering committee21 included Vandana Shiva, Corinne Lepage (former environment minister of France), Giles-Eric Séralini (toxicologist researching toxicities of GMOs and glyphosate), and Olivier De Schutter (former U.N. Special Rapporteur on the Right to Food), among others. The legal opinion on the evidence presented at the tribunal was delivered April 18, 2017. As reported by Corporate Europe Observatory:22 “The tribunal concluded that:

  • Monsanto has violated human rights to food, health, a healthy environment and the freedom indispensable for independent scientific research
  • ‘Ecocide’ should be recognized as a crime in international law
  • Human rights and environmental laws are undermined by corporate-friendly trade and investment regulation”

When asked if Bayer will continue Monsanto’s underhanded business practices, Baumann said the new entity will be managed “according to our standards,” adding that “Bayer stands for transparency, reliability and a different style of debate.”

Monsanto — A Destroyer of the Natural World

In addition to GE seeds and its flagship product, Roundup, Monsanto has also been a leading producer of Agent Orange, PCBs, DDT, recombinant bovine growth hormone and aspartame — the history of which is summarized in “The Complete History of Monsanto, ‘The World’s Most Evil Corporation,’”23 originally published by Waking Times in 2014.24

Monsanto also made its mark on history by participating in the Manhattan Project to build the first atomic bomb, thereby becoming a “war horse” ally to the United States government — an alliance that still holds today. As noted in “The Complete History,” article:

“To add insult to world injury, Monsanto and their partners in crime Archer Daniels Midland, Sodexo and Tyson Foods write and sponsor The Food Safety Modernization Act of 2009: HR 875.25 This ‘act’ gives the corporate factory farms a virtual monopoly to police and control all foods grown anywhere, including one’s own backyard, and provides harsh penalties and jail sentences for those who do not use chemicals and fertilizers. President Obama … gave his approval.

With this Act, Monsanto claims that only GM [genetically modified] foods are safe and organic or homegrown foods potentially spread disease, therefore must be regulated out of existence for the safety of the world … As further revelations have broken open regarding this evil giant’s true intentions, Monsanto crafted the ridiculous HR 933 Continuing Resolution,26aka Monsanto Protection Act, which Obama robo-signed into law as well.

This law states that no matter how harmful Monsanto’s GMO crops are and no matter how much devastation they wreak upon the country, U.S. federal courts cannot stop them from continuing to plant them anywhere they choose. Yes, Obama signed a provision that makes Monsanto above any laws and makes them more powerful than the government itself.”

Bayer Also Has a Long, Dark, Destructive History of Genocide

Despite having a far “cleaner” public reputation than Monsanto, Bayer is really just more of the same. Founded in Germany in 1863 by Friedrich Bayer and Johann Wescott, it too has a long, sordid history of creating poisons and mass destruction.27 During World War II, Bayer (then I.G. Farben) produced Zyklon B gas, used in the Nazi gas chambers to eradicate 11 million people whose only crime was to be born a Jew.

According to Alliance for Human Research Protection, the company was also “intimately involved with the human experimental atrocities committed by Mengele at Auschwitz.”28 In one case, Bayer purchased 150 healthy female prisoners from the camp commander of Auschwitz for use as test subjects for a new sleep drug. All the test subjects died, and another order for prisoners was placed.

While some of its board members ended up being arrested and tried for their crimes against humanity, others escaped and helped create the Federal Reserve.29 If you think the passing of time might have made this corporate entity kinder, safer and gentler, think again.

In 2003, it was revealed Bayer sold blood-clotting medicine tainted with the HIV virus to Asian, Latin American and Europe in the mid-1980s.30 The drug, Factor VIII concentrate, was worth millions of dollars, and the company continued to sell the tainted drug for a year after the contamination was discovered. In Hong Kong and Taiwan alone, more than 100 hemophiliacs contracted HIV and died after using the medicine.

Bayer’s drug Trasylol — used to control bleeding during surgery — was also eventually found to be responsible for at least 1,000 deaths each month for the 14 years it was on the market.31 In 2006, documents proved Bayer hid evidence showing unfavorable results from the drug in order to continue selling it.  Lawsuits have also been filed against Bayer for the untimely death of 190 young women taking their birth control pill Yaz, which raises your risk of blood clots by 300 percent.

Bayer Unlikely to Shift Public Perception of GMOs and Toxic Agriculture

Between 2006 and 2007, Bayer was also responsible for contaminating U.S. rice imports with three unapproved varieties of GE rice under development by Bayer CropScience. Bayer also makes neonicotinoid pesticides, suspected of being responsible for mass die-offs of bees around the world, thereby threatening the global food supply, and made the plastic chemical bisphenol-A, now known to have a dangerous impact on the human endocrine system.

In short, Bayer’s history is just as dark and unethical as Monsanto’s, if not more, and some have rightfully referred to the merger of these two destructive behemoths as a “marriage made in hell.”32 While change is possible, it seems improbable that this new Bayer-Monsanto mega-entity will radically change, and based on their combined histories, the world better get ready for a monumental fight.

Biotech Companies Are Gaining Power by Taking Over the Government

Monsanto and their industry allies will not willingly surrender their stranglehold on the food supply. They must be resisted and rolled back at every turn. There is no doubt in my mind that GMOs and the chemical-intensive agricultural model of which they are part and parcel, pose a serious threat to the environment and our health. Yet, government agencies not only turn a blind eye to the damage they are inflicting on the planet, but actively work to further the interests of the biotech giants.

This is not surprising. It is well-known that there is a revolving door between regulatory agencies and private corporations. This has allowed companies such as Monsanto to manipulate science, defang regulations and even control the free press, all from their commanding position within the halls of government.

Consider for a moment that on paper, the U.S. may have the strictest safety regulations in the world governing new food additives, but has repeatedly allowed GMOs and their accompanying pesticides such as Roundup to circumvent these laws.

In fact, the only legal basis for allowing GE foods to be marketed in the U.S. is the FDA’s tenuous claim that these foods are inherently safe, a claim which is demonstrably false. Documents released as a result of a lawsuit against the FDA reveal that the agency’s own scientists warned their superiors about the detrimental risks of GE foods. But their warnings fell on deaf ears.

Don’t Be Duped by Industry Shills!

In a further effort to deceive the public, Monsanto and its cohorts spoon-feed scientists, academics and journalists a diet of questionable studies that depict them in a positive light. By hiring “third-party experts,” biotech companies are able to take information of dubious validity, and present it as independent and authoritative.

Industry front groups also abound. The Genetic Literacy Project and the American Council for Science and Health are both Monsanto-funded. Even WebMD, a website that is often presented as a trustworthy source of “independent and objective” health information, is heavily reliant on advertising dollars. It is no coincidence that they promote corporate-backed health strategies and products.

There’s No Better Time to Act Than NOW — Here’s What You Can Do

The biotech giants have deep pocketbooks and political influence, and are fighting to maintain their position of dominance. It is only because of educated consumers and groups like the Organic Consumers Association (OCA) that their failed GMO experiment is on the ropes. We thank all of the donors who helped OCA achieve their fundraising goal. I made a commitment to triple match all donations to OCA during awareness week. It is with great pleasure to present a check to this fantastic organization for $250,000.

At the end of the day, we must shatter Monsanto’s grip on the agricultural sector. There is no way to recall GMOs once they have been released into the environment. The stakes could not be higher. Will you continue supporting the corrupt, toxic and unsustainable food system that Monsanto and its industry allies are working so hard to protect?

For more and more people, the answer is no. Consumers are rejecting genetically engineered and pesticide laden foods. Another positive trend is that there has been strong growth in the global organic and grass fed sectors. This just proves one thing: We can make a difference if we steadily work toward the same goal.

One of the best things you can do is to buy your foods from a local farmer who runs a small business and uses diverse methods that promote regenerative agriculture. You can also join a community-supported agriculture (CSA) program, where you can buy a “share” of the vegetables produced by the farm, so that you get a regular supply of fresh food. I believe that joining a CSA is a powerful investment not only in your own health, but in that of your local community and economy as well.

In addition, you should also adopt preventive strategies that can help reduce the toxic chemical pollution that assaults your body. I recommend visiting these trustworthy sites for non-GMO food resources in your country as well:

Organic Food Directory (Australia) Eat Wild (Canada)
Organic Explorer (New Zealand) Eat Well Guide (United States and Canada)
Farm Match (United States) Local Harvest (United States)
Weston A. Price Foundation (United States) The Cornucopia Institute

Monsanto and its allies want you to think that they control everything, but they are on the wrong side of history. It’s you, the informed and empowered, who hold the future in your hands. Let’s all work together to topple the biotech industry’s house of cards. Remember — it all starts with shopping smart and making the best food purchases for you and your family.

US Technological Transformations and the Narcotic-Fueled Genocide of American Workers

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By James Petras

Source: The Unz Review

Introduction

During his recent visit to New Hampshire on 3/20/18, President Trump declared once again that the US is facing a ‘drug epidemic’. This time he advocated the death penalty for criminal drug dealers as the solution to a national crisis that has killed over 1 million Americans since the 1990’s (when the blockbuster prescription opiate Oxycontin was first released on the market). Trump promised that the Justice Department would develop the most severe penalties for criminal drug traffickers, by which he meant foreigners. He argued that his proposed “Wall” (between the Mexican- US border) would cut the flow of drugs responsible for the ongoing addiction of millions of US citizens – as though the prescription opiate addiction epidemic resulted from a foreign invasion, and not corporate decisions from Big Pharma.

President Trump’s claim that 116 ‘drug deaths’ occur every day (42,000 a year) is a major underestimate. In 2017, alone over 64,000 drug overdose deaths were reported in official statistics (with many unreported cases signed off as natural or undetermined, especially in counties too poor to afford autopsies and expensive forensic toxicology). Another 4 million Americans, at least, are currently addicted to opioids and at risk for overdose.

In comparative terms, more American workers have been killed or devastated by narcotics (mostly via prescription) in 2017 alone, than in the entire decade of the Vietnam War with its 58,000 dead and 500,000 wounded. In 2017, 40,000 Americans died in motor vehicle accidents and another 39,000 by gun violence – and these statistics are not broken down to include vehicular accidents due to drug intoxication or gun violence over drugs. Prescription or illegal opiates, alone or mixed with other sedative drugs, like Valium, or alcohol, are the most prominent and preventable cause of premature death in the United States today.

This pattern is unique to the United States, where the irresponsible medical prescription of highly addicting narcotics has been the primary portal of entry into the degrading life of addiction for millions. Despite President Trump’s claims, the addiction crisis is not a product of urban Afro-American street dealers or Mexican narco-traffickers: This uniquely American crisis has been created and fueled by billionaire-owned US pharmaceutical corporations, which produced, distributed and wildly profited from legal narcotics. They were aided by the irresponsible prescription practice of tens of thousands of doctors and other ‘providers’ who introduced millions of vulnerable patients to the world of narcotic dependency – including youngsters with sports injuries and workers with job-related pain. These are physicians and medical providers who rarely stopped to examine their own responsibility, even when their otherwise healthy patients overdosed or were destroyed by addiction. It is especially outrageous that doctors and ‘Big Pharma’ worked hand in hand for over 20 years to create this epidemic, enjoying wild profits and almost total legal immunity. Few have dared to openly question their irresponsibility and greed. In the poorest and most vulnerable areas of this country, the most irresponsible and unaccountable incompetence has replaced real medical care and created a health care apartheid.

The Federal Drug Enforcement Agency (FDA) and the Drug Enforcement Agency (DEA) have protected the corporate drug traffickers and ensured the manicured and cultured narco-bosses the highest rates of return on their products. These polished pushers have their names engraved on the walls of museums and opera houses around the country.

The majority of Presidential, Federal, State and municipal candidates from both major parties have received millions of dollars in electoral campaign funds from these huge legal narcotic manufacturers and distributors, as well as from physicians and other representative of the ‘pain-treatment industry’. Over the past decades, politicians have openly or secretly opposed or weakened legislation designed to address this crisis.

Why not just ask President Trump to direct his Justice Department to impose the death penalty on the board of directors of the big corporate narcotic manufacturers or distributors or on the CEOs of major ‘pain clinics’ or on the owners of local rural ‘health centers’ that drove the villagers of West Virginia into their life-destroying downward spirals?

When will the DEA finally storm the medical centers to arrest the over-prescribing ‘providers’ of narcotics and benzodiazepine tranquilizers (a very common deadly combination)?

When will the SWAT teams seize the vacation homes of the CEOs of major US hospitals where the convenient and fake ideology of promising a ‘pain-free’ experience (‘make it Zero on the Pain Scale’) led to the generalized promotion of highly addicting narcotics for minor injuries, arthritic pain, or chronic back discomfort due to work or obesity? Responsible alternatives existed and were used in the rest of the world – largely untouched by this prescription-fueled crisis.

No doubt what President Trump has in mind is something else: the expulsion of Latin American workers under the pretext of going after the drug dealers and the even more massive incarceration of petty street dealers in the African American community.

Trump will then turn to further monitoring and arresting small-scale American marijuana farmers, who earn a basic income from growing a product that many believe is safe, non-addicting, and significantly reduces demand for dangerous narcotics.

As ugly as this all seems, the complicity of the political, economic and the medical elite in exponentially spreading deadly narcotics among the poor, working class and downwardly mobile middle class, points to a deeper and more sinister policy goal: the systematic elimination of millions of American workers made redundant in the new economy. This is a ‘gentler genocide’, where millions of workers die prematurely seeking an escape from pain as they have been replaced by a new technology and a new ideology: Robots, artificial intelligence and digitalization have rendered them disposable, while the out-sourcing of work to low paid overseas laborers and immigrants have guaranteed unimaginable profits for the elite decision makers.

This highly profitable process, benefiting the political, pharmaceutical, financial, police and judicial elites, conveniently blames the victims, a significant proportion of whom come from the poor and working class in this country, including white rural and small town addicts, especially youth, stuck at minimum wage jobs with no prospects of a decent future – injured construction workers, 15% of whom abuse prescription narcotics for work-related injuries, as well as the marginalized petty drug dealers from the urban slums and desperate Latino immigrants forced to accommodate the cartels. These people have little rights and are easily monitored, incarcerated, expelled and just written-off in one-line obituaries.

The narcotic-fueled genocide had grown out of a calculated corporate strategy meant to cull and subdue a huge population of potentially restive marginalized workers and their families, blaming the overdosing victims for their own ‘irresponsible’ choices, their reliance on prescription opiates, their lack of access to competent medical care, and their untimely deaths as though this were all a collective suicide as the great nation marches forward.

The higher the death toll among marginalized Americans, the greater the reliance on political distractions and racist deceptions. President Trump loudly blames street-level retail distributors, while ignoring the links between tax-exempt mega-billionaires who have profited from the shortened life-expectancies of addicted workers (scores of billions of dollars already saved in future pension and health care expenses) and the millions fired for addiction and denied jobless benefits and treatment. Trump has yet to even mention the actions of the legal pharma-medical industry that set this in motion.

Meanwhile, the Democratic Party leaders denounce the worker-victims of addiction and their communities as ‘irresponsible and racist’, for having believed the populist rhetoric of candidate Trump. Trump’s most intense rural areas of support coincided with areas of the worst opioid addiction and suicide rates. Trump’s rival, Hillary Clinton wrote off scores of millions of vulnerable Americans as ‘deplorables’ and never once addressed the addiction crisis that grew exponentially during her husband’s administration.

Since the implementation of NAFTA during the 1990’s, scores of millions of American workers have been relegated to unstable, low paid jobs, deprived of health benefits and subject to grueling work, prone to physical and mental injuries. Workplace injuries set the stage for the prescription narcotic crisis. Even worse, today workers are constantly distracted by electronic gadgets at the workplace, with their orders from above arriving digitally. These highly profitable gadgets have created enormous distractions and contributed to workplace death and injuries. The plaything of choice for the masses, the I-phone, has added to the addiction crisis, by increasing the rate of injury. This mind-numbing distraction, produced abroad at incredible profit, has played an unexplored role in the increase in premature death in the US.

The corporate narcotic elites, like the ultra-cultured Sackler clan owners of Perdue Pharmaceuticals, and their allies in the finance sector, support the diverse ideological distractions fashioned by their politician pawns: Eager to please her donor-owners, Hillary Clinton and the Democrats blame the working class for their backwardness and genetic propensity to addiction and degradation. Meanwhile, President Trump and the Republicans blame ‘outside’ suppliers and distributors including Mexican narco-cartels, illegal immigrant traffickers, black urban street dealers and now point to overseas Chinese fentanyl labs – as though the entire crisis came from the outside. Trump’s approach flies in the face of the unquestionable source of most narcotic addiction in the US: Irresponsible prescribing of highly addicting legal narcotics.

No other industrialized country is experiencing this scale of addiction and pre-mature death. No other industrialized country relies on a private, for-profit, unregulated system of delivering medical care to its citizens. Only the US.

Both elite political parties avoid the basic issue of the long-term, large-scale structural imperatives underlying the transformation of the US work places. They refuse to address the marginalization of tens of millions of American workers and their families, made disposable by corporate economic and political decisions.

The US corporate elite are completely incapable of developing, let alone favoring, any policy that addresses the needs of millions of surplus office and factory workers and their family members replaced by new technology and ‘global’ economic policies. The American financial and political elite is not about to support an economic, political and cultural ‘GI’ bill to save the scores of millions shoved to the wayside in their rush to obscene wealth and power.

The unstated, but clearly implemented, ‘final solution’ is a Social Darwinian policy of active and passive neglect, the unleashing of profitable prescription narcotics into the population of vulnerable disposable workers, offering them a convenient, painless way out – the opioid solution to the over-population problem of redundant rural and small town ‘Helots’. The political elite’s willing complicity with Big Pharma, the medical profession, the financial oligarchs and the prison-industrial complex has transformed the country in many ways. Shortened lives and depopulation of rural and small town communities translates into lower demand for public services, such as schools, health care, pensions and housing. This is guaranteeing a greater concentration of national wealth in the hands of a tiny elite. The financial press has openly celebrated the projected decrease in pension liabilities as a result of the drop in worker life expectancy.

The ongoing mass genocide by opioids may have started to arouse popular discontent among working people who do not want to continue dying young and miserable! Social services and child protective services for the millions of orphaned or abandoned children of this crisis have been demanding real policies. Unfortunately, the usual platitudes and failed policies prevail. Drug education and ‘opioid addiction treatment’ programs (currently among the largest expense in some union health plans) are pointless Band-Aids when confronted by the larger policy decisions fuelling this crisis. Nevertheless, thousands of health care professionals are beginning to resist corporate pressure to prescribe cheap opioids – and fight for more expensive, but less dangerous, alternative for addressing their patients’ pain. Even if all medical providers stopped over-prescribing narcotics today, there are still millions of addicts already created by past practice, who seek the most deadly street drugs, like fentanyl, to feed their addiction.

Politicians now publicly denounce ‘Big Pharma’, while privately winking at the lobbyists and accepting millions from their ‘donor-owners’.

Public critics in the corporate media are quick to condemn the workers’ susceptibility to narcotic addiction but not the underlying causative imperatives of global capitalism.

Mainstream academics celebrate corporate technological advances with occasional neo-Malthusian warnings about the dangers of millions of redundant workers, while ignoring the profit-driven role of narcotics in reducing the social threat of excess workers!

Finally the role of an elite and respected profession must be re-evaluated in a historic context: In the 1930’s German doctors helped develop an ideology of ‘racial hygiene’ and a technology to demonize and eliminate millions of human beings deemed redundant and inferior, through overwork in slave camps, starvation and active genocide – serving the ambitions of Nazi expansionism and deriving significant profit for select individuals and corporations. US physicians and the broader medical community have less consciously assisted in the ongoing ‘culling of the herd’ of American laborers and rural residents rendered superfluous and undesirable by the decisions of a global oligarchy increasingly unwilling to share public wealth with its masses. There are similarities.

Once prosperous, industrial cities and towns, as well as rural villages, in the US have seen marked declines in populations and a premature death crisis among those who remain.

This must be reversed.

 

The Weird Politics Of Aspartame: Conspiracy Theory Or Startling Truth?

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By Paanii Powell Cleaver

Source: Inquisitr

Earlier this month, news wires and Twitter feeds were abuzz with info about the potential danger of certain artificial sweeteners.

In reality, recent reports about the potential perils of low-calorie sweeteners are not exactly breaking news. Almost 20 years ago, on December 29, 1996, Mike Wallace conducted an eye-opening segment about aspartame, also known as NutraSweet, on 60 Minutes.

The segment aired in response to a flurry of reports noting a dramatic increase in brain tumors and other serious health issues following the approval of aspartame for use in dry foods in 1981. Fifteen years after its somewhat dubious approval, (the most controversial FDA decision to date), more than 7,000 consumer reports of adverse reaction to aspartame had been delivered to the FDA. As reported by 60 Minutes, the litany of consumer complaints included severe headaches, dizziness, respiratory issues, and seizures. The FDA countered with a statement that aspartame was the most tested product in FDA history.

Dr. Virginia V. Weldon, a pediatrician from Missouri and Vice President of Public Policy for the Monsanto Company from 1989 through 1998, told 60 Minutes that aspartame is “one of the safest food ingredients ever approved by the Food and Drug Administration.”

Dr. John W. Olney, a neuroscientist at Washington University School of Medicine, vehemently disagreed with Dr. Weldon’s assessment of the controversial super sweetener. Notable for his discovery of the brain-harming effects of an amino acid called glutamate, Dr. Olney was influential in legislating the ban of MSG in baby food. At the time of the 60 Minutes segment, he had been studying the effects of aspartame and other compounds on brain health for more than two decades.

Olney told 60 Minutes’ Mike Wallace that since the approval of aspartame, there had been “a striking increase in the incidence of malignant brain tumors.” The doctor did not directly blame aspartame for the increase. He did, however, state that there was enough questionable evidence to merit reevaluating the chemical compound. He said that the FDA should reassess aspartame and that “this time around, they should do it right.”

Dr. Erik Millstone, Professor of Science Policy at the University of Sussex, told 60 Minutes that Searle’s testing procedures in the early 1970s were so flawed that there was no way to know for certain if aspartame was safe for human consumption. Millstone claimed that the company’s failure to dissect a test animal that died during an aspartame experiment was merely one example of “deficiencies” in Searle’s conduct. He also noted that when test mice presented with tumors, the tumors were “cut out and discarded and not reported.” In addition, Dr. Millstone told Mike Wallace that G.D. Searle and contractors hired by the drug company administered antibiotics to some test animals yet neglected to reveal this information in official reports.

In 1974, after the G.D. Searle company had already manufactured a significant quantity of aspartame, then-commissioner of the FDA, Alexander Schmidt, came very close to approving the chemical for human food purposes. Relying solely on evidence provided by Searle, the FDA allowed a mere 30 days for the public to respond before putting the FDA seal of approval on the now-controversial food additive. Dr. John Olney wasted no time in joining forces with James Turner, a public interest attorney who also worked with consumer advocate Ralph Nader. Just before the allotted time for public response ran out, Dr. Olney and his attorney petitioned the FDA with data that indicated the dangerous similarities between aspartame and glutamate.

In his 1970 best seller, The Chemical Feast, Turner detailed numerous ways the FDA shirked its obligation to protect the American people. At the time of its publication, Time magazine described the tome as “the most devastating critique of a U.S. government agency ever issued.”

In response to Dr. Olney’s allegations that aspartame was potentially as brain-damaging as glutamate, the FDA called for a task force to investigate the matter. By late 1975, the FDA found that Searle’s own research into the safety of aspartame was so flawed that they stayed the approval process, citing “a pattern of conduct which compromises the scientific integrity of the studies.”

Former U.S. Senator Howard Metzenbaum told 60 Minutes that when Searle presented information to the FDA in 1974, the drug company “willfully misrepresented” and omitted facts that may have halted approval of what would soon become its best-selling product. Metzenbaum went on to say that the FDA was so disturbed by its findings, it forwarded a file to the U.S. Attorney’s Chicago office in 1975 in the interest of calling a grand jury to determine whether criminal indictments against Searle were warranted.

When did the grand jury convene? Never. According to 60 Minutes, U.S. Attorney Samuel Skinner requested a grand jury investigation in 1977 but recused himself from the case when he was offered a job at the Sidley & Austin law firm, which also happened to be the Chicago law firm that represented the G.D. Searle company. The investigation was stalled until the statute of limitations ran its course, and no grand jury ever heard the case against Searle’s questionable research standards. Skinner, by the way, did eventually accept the job with Searle’s Chicago law office.

In 1977, a new FDA task force convened in Skokie, Illinois, with the sole purpose of investigating the research methods employed by G.D. Searle in its effort to gain FDA approval of aspartame. The task force examined raw data from 15 studies that Searle used to back up its uniformly positive claims about aspartame. According to journalist Andrew Cockburn, the task force noted numerous “falsifications and omissions” in Searle’s research reports.

In 1980, at the tail end of the Carter administration, the FDA conducted two-panel investigations into claims that aspartame caused brain tumors. Led by scientific and medical experts, each panel concluded that more tests were needed to prove the safety of the sweetener. Both panels concluded that aspartame should not be approved at that time.

So, how does the fellow in the cover picture figure into this equation?

If you do not recognize the face in the feature photo, here is a memory refresher: The man in the pic — and up to his ears in the aspartame controversy — is Donald Rumsfeld. Perhaps best known as Secretary of Defense during the George W. Bush presidency, Donald Rumsfeld also happened to be CEO of the G.D. Searle drug company when Ronald Reagan was sworn in as President of the United States on January 1981.

Regardless of its safety or potential peril, the fact remains that without the clout and political influence of Donald Rumsfeld, aspartame might never have been approved for human use at all.

Donald Rumsfeld, who at one time aspired to be Reagan’s running mate, was a member of the new president’s transition team. Part of the team’s duties involved the selection of a new FDA Commissioner. Rumsfeld et al chose a pharmacist with no experience in food additive science to lead the agency.

On January 21, 1981, Ronald Reagan’s first full day as president, the G.D. Searle company, headed by Donald Rumsfeld, reapplied for FDA approval of aspartame. That same day, in one of his first official acts, President Reagan issued an executive order that rescinded much of the FDA commissioner’s power.

In April 1981, newly appointed FDA commissioner Arthur Hayes Hull, Jr., put together a five-person panel tasked to reevaluate the agency’s 1975 decision to not approve aspartame as a food additive. At first, the panel voted 3-2 to uphold non-approval of the chemical sweetener. Hayes then invited another member to the official FDA panel, and the vote was retaken. The panel deadlocked, and Hayes contributed his own vote to break the tie. Two months later, the product that the FDA refused to approve for seven long years was suddenly approved for human consumption.

Four years later, in 1985, the Monsanto corporation bought G.D. Searle and established a separate division, The NutraSweet Company, to manage the sales and public relations of one of its best-selling and most profitable products. It may be worth noting that when Monsanto purchased Searle and the patent on aspartame, Donald Rumsfeld reportedly received a fat $12 million bonus.

Before reading this, how much did you know about the origins of aspartame? If you’re like most Americans, the answer is “not much.” And, if you’re like many Americans, your interest in a story such as this one will wane as soon as the next hot topic comes along. Perhaps this is the reason that there has been little if any public outcry regarding aspartame or the weird way that it received FDA approval.

Updates:

In 1987, UPI investigative journalist Gregory Gordon reported that Dr. Richard Wurtman, a neuroscientist at Massachusetts Institute of Technology and a die-hard supporter of aspartame during its 1981 rush to approval, had reversed his thoughts on the sweetener. He noted the once-ardent supporter as saying his views had evolved along with scientific studies and his increased skepticism of industry research standards.

In 1997, the U.K. government obliged makers of sweetened food to prominently include the words “with sweeteners” on product labels. Ten years later, U.K. supermarket chain Mark & Spencer announced the end of artificial sweeteners and coloring in their chilled goods and bakery departments, according to the Daily Mail.

In his well received 2007 book, Rumsfeld: His Rise, Fall and Catastrophic Legacy, author Andrew Cockburn described the results of the 1977 FDA task force that found “falsifications and omissions” in Searle’s research data. The New York Times called author Cockburn’s biographical tome “quite persuasive.”

In 2009, Woolworths, a South African retailer, announced that it would no long brand products containing aspartame.

On February 28, 2010, Dr. Arthur Hayes Hull, Jr., the FDA Commissioner who hurried aspartame to market and later squelched public fear of Tylenol during the 1982 poisoning scare, died in Connecticut. According to his New York Times obituary, Hayes was employed as president of E. M. Pharmaceuticals after his term at the FDA. Hayes succumbed to leukemia at age 76.

A 2011 report in the Huffington Post noted that 10,000 American consumers notified the FDA about the ill effects of aspartame between 1981 and 1995. According to the article, the use of aspartame elicited more complaints than any other product in history, comprising 75 percent of complaints received by the U.S. Food and Drug Administration.

In 2013, the EFSA (the British equivalent of the FDA), reiterated its claim that aspartame is harmless. Professor Erik Millstone responded with his own reevaluation of aspartame, in which he noted that every study the EFSA used to approve aspartame was funded by the same industry that manufactures and profits from the controversial sweetener.

Dr. John W. Olney passed away at the age of 83 on April 14, 2015. In addition to his campaigns against aspartame and glutamate, the doctor devoted half a century of his life to finding a cure for Multiple Sclerosis, the crippling neurological disease that claimed his own sister when she was 16. According to the St. Louis Post Dispatch, cause of death of the pioneering brain researcher included complications of ALS, a neurological disorder more commonly known as Lou Gehrig’s Disease.

Those interested in learning more about the approval of aspartame are invited to read the FDA Commissioner’s Final Report, published by the Department of Health and Human Services on July 24, 1981. A detailed version of the aspartame timeline is available at Rense.com.