Category Archives: Moderna

Back at Ground-Truthing Again and Again and Again

Time and time again, the left sites just keep pushing all those international stories, all those stories tied to this or that political party head, and while China is important, and while we know the dirty deeds of Blinken to Pompeo, all the way back, we still miss out on the common people, us, the little ones.

Sure, this is a trending story, in California, tied to the vaccine mandate, the hysteria, the fascism:

The University of California, Irvine has placed their Director of Medical EthicsDr. Aaron Kheriaty, on ‘investigatory leave’ after he challenged the constitutionality of the UC’s vaccine mandate in regards to individuals who have recovered from Covid and have naturally-acquired immunity.

Last month Kheriaty, also a Professor of Psychiatry at UCI School of Medicine, filed a suit in Federal court over the mandate.

Natural immunity following Covid infection is equal to (indeed, superior to) vaccine-mediated immunity. Thus, forcing those with natural immunity to be vaccinated introduces unnecessary risks without commensurate benefits—either to individuals or to the population as a whole—and violates their equal protection rights guaranteed under the Constitution’s 14th Amendment,” Kheriaty wrote in a Sep. 21 blog post.

“Expert witness declarations in support of our case include, among others, a declaration from distinguished UC School of Medicine faculty members from infectious disease, microbiology/immunology, cardiology, endocrinology, pediatrics, OB/Gyn, and psychiatry,” the post continues (click here to read the rest).

…there is now considerable evidence that Covid recovered individuals may be at higher risk of vaccine adverse effects compared to those not previously infected (as seen in studies herehere, and here, among others). -Dr. Aaron Kheriaty

This issue, though, is more important on a local level for schmucks like me, who are overeducated, aging in a hateful society, left of left in a centrist and capitalism hard left/right contradictory world. I am back at a job, and the pay is embarrassing, and the fact that I am in a rural county with rural thinkers and with a service economy tied to beach combing, fishing, crabbing and vacation rentals also contributes to precarity.

You think I am ready to leave to go somewhere else, to some big sophisticated city, some harbinger of high tech and military industrial complex to find more sustainable and lucrative work? Each day, my skill sets, my background, all the ground-truthing and other on the job training, all the travel, all those deep learning moments in my life in several fields, all of that is mush to the masters of academia, the masters of companies that are small and large, getting on the gravy train of city, county, state, national and international money. Tax cheats and welfare queens and kings are those in the complex, the big C for the CRC, Corruption Racket Complex — military-banking-ag-energy-prison-pharma-education-medicine-mining-chemical-AI-surveillence-real estate-insurance-prison-legal-media-entertainment.

Yep, bad that an environmental lawyer was under ankle bracelet house arrest for more than two years and faces six months in jail for contempt as a lawyer who sued the pants off of Chevron for killing and polluting communities south of this border. Sure, the hellfire and brimstone of this rotting empire is addictive, with all these blogs and newsfeeds and whatnot tapping into the lizard part of the collective American brain.

Chevron Steven Donziger Feature photo

Judge Loretta Preska, an advisor to the conservative Federalist Society, to which Chevron is a major donor, sentenced human rights attorney and Chevron nemesis Steven Donziger to six months in prison Friday for misdemeanor contempt of court after he had already spent 787 days under house arrest in New York.

Preska’s caustic outbursts — she said at the sentencing, “It seems that only the proverbial two-by-four between the eyes will instill in him any respect for the law” — capped a judicial farce worthy of the antics of Vasiliy Vasilievich, the presiding judge at the major show trials of the Great Purges in the Soviet Union, and the Nazi judge Roland Freisler who once shouted at a defendant, “You really are a lousy piece of trash!”

full image
Original illustration by Mr. Fish

So, note the “proverbial two-by-four between the eyes” comment from this judicial devil . . . . From a multimillionaire “judge.” Imagine that! If I told a pig that exact same thing, after stopping me for a dangling mud flap on my minivan, just think what might happen to me. Or if I told that she needed a proverbial two by four between the eyes to a judge during my trial or someone else’s? Or, to the boss, uh? Or to the teacher if I was an 11th grader. Or, to the drill sergeant? Or the TSA guy smelling my feet at the airport.

This judge is human scum, and while this is of national and international importance, I have been in courtrooms (local, small and midsized town) where women lost their children, where drug addicted got the book thrown at them, where homeless rough sleepers were fined and incarcerated, where people more sane than this judge were committed to mental ward. This is the truth about systems of oppression, about modern white civilization, a fucked up rule of law lawlessness. This is it in our world. But it happens every day a few ten thousand times. To we the small ass people.

Now, multiple that by a factor a ten thousand — try suing Boeing, or Pfizer or FDA, or Ford, or General Mills, or Bayer, or Trump Towers or Bank of America, or Amazon, or Google, or the manufacturer of the air bag in the minivan or the pretzel maker  your kid is choking on.

Now, bring it back to a real perspective. Local, where cities have no money for infrastructure, where medical systems are threadbare at least, or missing altogether. No country for old men, for young people, for the sick, disabled, poor, mentally challenged, psychiatrically impaired. This is a country for no regular people.

Paperback No Country for Old Men Book

Yet, we will hear the media mental midgets yammer on and on about us bumkins, us flyover fucks, deplorables, or deploying any other laundry list of pejoratives or socio-psych mumbo jumbo for their elite brains to find more ways to subjugate the many in the name of profits, and in the words of their deep alter egos — “The world of elites and beautiful and worthy and good members of society have to deal with these useless breeders, breathers and eaters. Really, all we want is what’s best for the masses, for these misbegotten, less than high IQ, and multiple-dysfunctional people who in some cases, well, don’t mean to be useless eaters, breeders, breathers, existers. But we can corral them into good deeds, and we can make so much money from their faults, chronic illnesses, their low IQ’s, their inbreeding, their constant bad bad bad decisions in life. Their mistakes and pain and dysfunction are our opportunity to make society the way we want it designed, with a few trillion of profits in greenbacks to boot. But we would never say this outright to Anderson Cooper or Oprah or NPR or what not.”

But reality is always local, no matter how much bullshit college sports and pro football teams and idiotic Republican and Democrat lying and spewing interferes with their noggins. For example, the outfit I work with, as a social services guy, doesn’t ask our clients — developmental and intellectual disabled adults — if they have had “the jab,” but rather, they ask: “If an employer asks you to provide proof of vaccination, will that be a problem?”

That is the reality now — adults barely surviving, after their whole lives have been spent in special ed programs and being evaluated, separated, roomed, housed and institutionalized, and many coming from proverbial messed up families, dysfunction being the functional word — I have to navigate more of the same systems of oppression-poverty inducing-safety net fraying eating at our communities’ very souls. The chances of getting part-time work in a field tied to the five F’s (food, fur, factory, filth, foliage — restaurants, dog cleaning, warehouses, janitorial, and landscaping) are already slim, as so much is stacked against these folk. Think about the propaganda around “those with developmental disabilities are more vulnerable to the covid so they need to be vaxxed first” ideology.

Many clients were so scared that they were more or less forced into getting the Pfizer or J & J, both mRNA biomedical experimental treatments. Most live in supported housing, and most of these in group homes, sanctioned by the state, so the vaccine mandates are not just inferred, but demanded. Boosterism (booster x, y, z, omega) will continue to run rampant. More will be sick. Some will die, or course.

The reality is I know people who are losing jobs, and they are not sitting on piles of cash like a lot of professionals you might read about that are opting out of the forced chemical jabs. These people do not have the luxury of taking a stand with unlimited credit card limits, or fully owned homes, or hobby gardens out back with the swimming pool. These are people who read up about this planned pandemic, who take precautions, who listen to experts. Their choice is to not get jabbed.

Imagine, being a teacher, PhD in physics, after  20 years, and you have 130 accrued sick days (paid) and you refuse to do the jab but accept the draconian test and mask. You are still going to be fired, or put on unpaid leave, and those PTO days you have accrued, well, forget about them.

LEAKED GRANT PROPOSAL DETAILS HIGH-RISK CORONAVIRUS RESEARCH
The proposal, rejected by U.S. military research agency DARPA, describes the insertion of human-specific cleavage sites into SARS-related bat coronaviruses.” (source)

This is reality for one of my friends. Forget about the death proclamations of the Death Cult of Fauci. This guy is criminal, and he has sold millions a bill of goods. This bill of goods is dangerous, deadly, injurious.

A bill of goods, man, the lies, the continuing criminal enterprises, and then, remade, make overs, etc. Take these middle of the road news sites: Robert Scheer is not my favorite, but this takes the cake, no, as he appears as Mister New York Times and Most About USA is Good Scheer. So, no doubts about this fellow joining up with the CIA, and then now in Holly-Dirt?

This is the very celebrity culture that Chris Hedges rails against. This is a sick little blurb here promoting Scheer’s podcast of this criminal — CIA is a criminal outfit of the highest order.

A former CIA officer and Emmy award-winning creator of the hit FX series “The Americans” about two Soviet agents living secretly in Washington during the Cold War, Weisberg offers a refreshing perspective on the tense relationship between the two countries throughout his work. He joins Robert Scheer on this week’s “Scheer Intelligence” to talk about his latest book, “Russia Upside Down: An Exit Strategy for the Second Cold War,” in which he examines how he, like so many Americans, got Russia wrong.

The author tells Scheer about his childhood growing up in a liberal Jewish household in Chicago, Ill. before studying Soviet politics at Yale University and joining the CIA, eager to do his “duty as an American” and fight what he considered then to be the “evil” Soviet empire. Now, after years of writing fiction about the Soviet Union in novels and TV scripts, Weisberg has decided to reflect on the historical events that he briefly played an active role in during his brief time at the CIA as the Soviet Union was collapsing through a more critical, factual lens. Based on both his personal experience as well as detailed research, Weisberg dispels common misconceptions about Russia that he once held to be true in “Russia Upside Down.”

Here we go: More meaningless Hollywood-CIA-millionaire stuff that the average Joe in Tucson or Portland, in Kansas or Utah has zero connection to. But we get he is Jewish (hmm, why this?) a Yale graduate (Yale being a CIA-Imperialist school), and lover of CIA and USA (when he was young — what puke). Fiction writer, and now a book writer and TV series producer, wow, what a radical.  This is the upper echelons of America Putridity, and you couple that with his millions thrown at him as a Holly-Dirt thing, and we have the mini-Celebrity fawning.

Scheer Intelligence Is America’s View of ‘Evil’ Russia Merely Projection?

The Americans: The Complete First Season (DVD)
More TV junk!

I was at a hospital two weeks ago, and the nurses must have thought I wasn’t awake (I never sleep in a hospital, in jail, or on a plane). They talked about the Samaritan Hospital system they work for introducing a “no vaccine, no medical service” protocol. They did not sound happy about it. And here we have it yesterday:

The Associated Press

Leilani Lutali, foreground, and Jaimee Fougner pose for a photo, Thursday, Oct. 7, 2021 in Colorado Springs, Colo. Lutali recently found out her hospital wouldn’t approve her kidney transplant surgery until she got the COVID-19 vaccine. Even though she has stage 5 kidney disease that puts her at risk of dying without a new kidney. (AP Photo/Thomas Peipert) — source

A hell of a country, and a hell of a “follow the science” kind of messed up system, no? Idiots of the Biden-Obama variety, like Thom Hartman, are yammering on and on about how these hospitals have a right to refuse un-jabbed folk. This is it for the liberals — you eat junk food, you drink booze, you suck on fags, you drive recklessly, you think this or that anti-Democratic Party thought, then we, the good beautiful, Hillary-Obama-Harris have a right to cut you off, cut you down, chop you off at the knees!

Many people I speak with and communicate with are tired of the pro-pro-pro forced jab perspective we are getting from the leftist Counterpunch, and from St. Clair.

I am referencing “Roaming Charges,” Counterpunch, 10/8/2921, from the anti-science pro-some-science get-out-of-that-science’s way thinking coming from some of the articles posted on the site. Very sad in many ways, so sad that there is not a robust discussion of the vaccination that we see on Dissident Voice, even Mint Press, and especially OffGuardian and Left Skeptics. Here, bullet points, direct quoting from “Roaming Charges”:

+ I’m against any exemptions (our social contract should require either all of us to get it or that the jab be completely voluntary ), but if there’s a religious exemption there should be one for philosophy, too. “Dr. Anthony Fauci says he’s worried that people resisting COVID-19 vaccine shots based on religious grounds may be confusing that with a philosophical objection.”

+ Merck is selling its high-touted new Covid pill Molnupiravir, whose development was federally financed by NIH and the Department of Defense,  back to the U.S. government for 40 times what it costs to make.

+ These people, if you want to call them that, seem to have taken their “tactics” from the Westboro (“God Hates Fags”) Baptist Church which used to (and I suppose still does) scream their godly obscenities at mourners during the funerals of people who died of AIDS.

+ Anti-vaxism is itself a kind of brain-eating virus…A Cumberland, Maryland man murdered his brother and sister-in-law in their Ellicott City home last week because his brother, a local pharmacist, had administered COVID-19 vaccines.

+ Cuba began vaccinating its population 150 days ago. In that time, it has administered 192 doses per 100 people. In contrast, the US began its vaccination program 297 days ago and has managed to administer only 119 doses per 100 people. The Covid death rate in Cuba is: 684 per million. The death rate in the US is: 2190 per million. This seems to provide pretty clear evidence that the embargo has been placed on the wrong country for the last 60 years. (end quote)

And therein lies the problem with fake leftists — attacking even doctors and virologists and journalists and educated/educators who have doubts about the entire pandemic and mRNA and coronavirus multiplicity of very pro-pro Capitalist and pro-pro Authoritarian and pro-pro Government Bureaucracy rhetoric. The reality is Cuba is not jabbing its people with mRNA: “All of Cuba’s vaccine candidates—Abdala, Soberana 1, Soberana 2, Soberana Plus, and Mambisa, are subunit protein vaccines, like the Novavax vaccine. Crucially, the vaccines do not require extreme refrigeration, are cheap to produce, and are easy for the country to manufacture at scale. They are made by fermentation in mammalian cells, a process Cuba already uses for monoclonal antibodies.”

A nurse holds up a vial of vaccine

Now, we are worried about more of the celebrities, this time, a professor who was sacked —

Now, think about any criticism against any university, when you are employed by the institution. I was employed by the University of Texas at El Paso. I was an English Department faculty, part-time, a radical, and I fought like hell for adjuncts, for students, etc. I was part of a group of students as a faculty member who made a human chain to stop the group of overweight sheriff posse dudes dressed up as Conquistadors on horses strutting on campus. That was 1992, the 500th anniversary of that evil contact we call Columbus Day. The El Paso Times ran a front page photo of these undercover cops jumping out of the bushes, and wrangling students, clobbering male and female with forearms to the neck. I was right in the middle, and I had to answer for myself to the Provost and president.

This is what a university, then, in 1992, was encapsulated inside, under a rich white president, a campus that was and still is 80-plus percent Mexican-American, Latinx, now. You can’t protest without our permission and our approval of signs!

More cities are recognizing Native Americans on Columbus Day

This was a campus that introduced a free speech zone out of the way of foot traffic. A state sponsored school, with a limited small postage stamp of land near dumpsters where people can gain the public square for protesting. And the campus Nazis demanded permission, permits, and full written details of the “protest” or “information gathering.” Now, sure, talk about Covid, about Nuremburg protocol, about mandates, about those who have the jab and those who do not. Talk about NIH and Fauci and the shadowy origins of the SARS-CoV2, or the doctors who have protocols to stop not only Covid patients getting on ventilators, but getting patients out of the hospital and back home in recovery zone. Not allowed.

These articles are verboten on campuses:

And, if I was still on that campus, how quickly would I be sacked for criticizing a campus– that pushes the Hispanic University of the World theme while colonizing Hispanics (mostly Mexican Americans) — for lock-step falling into the fold of the Corruption Racket Complex — military-banking-ag-energy-prison-pharma-education-medicine-mining-chemical-AI-surveillence-real estate-insurance-prison-legal-media-entertainment? This campus is the whoring field of military, aerospace, drone and weapons makers, and even more nefarious. What ugly optics! Four Star Murder Bomber Air Force General all smiles and the PhD’s just lapping up the uniform!

So, back into that ground-truthing — try being a radical, a revolutionary, a critic of bureaucracies and corporate mandates and this sort of bullshit on a local level. UTEP is a sell-out, an embarrassment, but so are most all the colleges and universities in this shit hole. (Source) I have gone up against every single college and university I have taught in. EVERY ONE.  Can you imagine bringing this into the classroom — anti-war, anti-military, anti-corporation discourse and readings and critical thinking debates? Shit! Then, this? Pfizer Exposed! 

And while the big house is for us in the 80 percent, the ground-truthing in your neighborhood is littered with the poisons of that Complex, the Continuing Criminal Enterprise called capitalism.

[The aim of the international bankers was] nothing less than to create a world system of financial control in private hands able to dominate the political system of each country and the economy of the world as a whole. This system was to be controlled in a feudalist fashion by the central banks of the world acting in concert, by secret agreements arrived at in frequent private meetings and conferences.

— Professor Carroll Quigley, Tragedy & Hope, p. 324 (source)

Finally, another point from a friend: “Fishy Felonious Fraudulent Fauci: Read Whitney Webb’s latest.”

During the panel, the moderator—Michael Specter of the New Yorker—asked the question: “Why don’t we blow the system up? Obviously, we just can’t turn off the spigot on the system we have and then say ‘Hey! everyone in the world should get this new vaccine we haven’t given to anyone yet,’ but there must be some way.” Specter then mentioned how vaccine production is antiquated and asked how sufficient “disruption” could occur to prompt the modernization of the existing vaccination development and approval process. Hamburg responded first, saying that as a society we are behind where we need to be when it comes to moving toward a new, more technological approach and that it is now “time to act” to make that a reality.

Several minutes later, Anthony Fauci stated that the superior method of vaccine production involves “not growing the virus at all, but getting sequences, getting the appropriate protein and it sticking in on self-assembling nanoparticles,” essentially referring to mRNA vaccines. Fauci then stated: “The critical challenge . . . is that in order to make the transition from getting out of the tried and true egg-growing [method] . . . to something that has to be much better, you have to prove that this works and then you have got to go through all of the critical trials—phase 1, phase 2, phase 3—and show that this particular product is going to be good over a period of years. That alone, if it works perfectly, is going to take a decade.” Fauci later stated that there is a need to alter the public’s perception that the flu is not a serious disease in order to increase urgency and that it would be “difficult” to alter that perception along with the existing vaccine development and approval process unless the existing system takes the posture that “I don’t care what your perception is, we’re going to address the problem in a disruptive way and an iterative way.”

During the panel, Bright stated that “we need to move as quickly as possible and urgently as possible to get these technologies that address speed and effectiveness of the vaccine” before discussing how the White House Council of Economic Advisers had just issued a report emphasizing that prioritizing “fast” vaccines was paramount. Bright then added that a “mediocre and fast” vaccine was better than a “mediocre and slow” vaccine. He then said that we can make “better vaccines and make them faster” and that urgency and disruption were necessary to produce the targeted and accelerated development of one such vaccine. Later in the panel, Bright said the best way to “disrupt” the vaccine field in favor of “faster” vaccines would be the emergence of “an entity of excitement out there that’s completely disruptive, that’s not beholden to bureaucratic strings and processes.” He later very directly said that by “faster” vaccines he meant mRNA vaccines.

The Bright-led BARDA and the Fauci-led NIAID in just a few months’ time became the biggest backers of the Moderna COVID-19 vaccine, investing billions and co-developing the vaccine with the company, respectively. As will be explained in Part II of this series, the partnership between Moderna and the NIH to co-develop what would soon become Moderna’s COVID-19 vaccine was being forged as early as January 7, 2020, long before the official declaration of the COVID-19 crisis as a pandemic and before a vaccine was proclaimed as necessary by officials and other individuals. Not only did the COVID-19 vaccine quickly become the answer to nearly all Moderna’s woes but it also provided the disruptive scenario necessary to alter the public’s perceptions of what a vaccine is and eliminate existing safeguards and bureaucracy in vaccine approval. (Watch the 2019 Universal Flu Vaccine event here.)

As Part II of this series will show, it was an alleged mix of “serendipity and foresight” from Moderna’s Stéphane Bancel and the NIH’s Barney Graham that propelled Moderna to the front of the “Warp Speed” race for a COVID-19 vaccine. That partnership, along with the disruptive effect of the COVID-19 crisis, created the very “Hail Mary” for which Moderna had been desperately waiting since at least 2017 while also turning most of Moderna’s executive team into billionaires and multi-millionaires in a matter of months.

However, Moderna’s “Hail Mary” won’t last – that is, unless the mass administration of its COVID-19 vaccine becomes an annual affair for millions of people worldwide. Even though real-world data since its administration began challenges the need for as well as the safety and efficacy of its vaccine, Moderna – and its stakeholders – cannot afford to let this opportunity slip through fingers. To do so would mean the end of Moderna’s carefully constructed house of cards.

The post Back at Ground-Truthing Again and Again and Again first appeared on Dissident Voice.

mRNA “Vaccines,” Eugenics, and the Push for Transhumanism

In 1989, researchers from the Salk Institute in California published a paper detailing how they developed an RNA transfection system that could “directly introduce RNA into whole tissues and embryos”. The concept of using RNA as a drug is first described in this paper, making it the seminal work that formed the foundation for decades of further research in this area. The “Discussion” section of the paper states that:

The RNA/lipofectin method can be used to directly introduce RNA into whole tissues and embryos (R.W.M., C. Holt, and I.M.V., unpublished results), raising the possibility that liposome-mediated mRNA transfection might offer yet another option in the growing technology of eukaryotic gene delivery, one based on the concept of using RNA as a drug.

One of the Salk Institute researchers listed on the paper is Dr. Robert W. Malone, a scientist who has recently been censored on social media for warning about the possible dangers of the covid-19 vaccines. It could be argued that there’s no expert more qualified to warn us about the dangers of mRNA injections than the man who helped pioneer the technology, nevertheless, Big Tech decided he was expounding “misinformation”, because, well, they know better apparently.

Malone’s research, which resulted in a procedure that could be used to “efficiently transfect RNA into human cells” using a “synthetic cationic lipid” was supported by grants from the American Cancer Society and the National Institute of Health (who currently have a stake in the Moderna mRNA vaccine, showing their allegiance to the technology. More on this later).

While Malone’s contributions to the development of mRNA technology are well-known and well-documented, Wikipedia decided to remove all mention of him from their “RNA Vaccine” entry shortly after the scientist began speaking out about the dangers of the rushed-through covid vaccines. The June 14th version of the article mentioned Malone by name 3 times and cited his work 6 times. The current version of the article mentions him 0 times and cites his work only 3 times.

However, this is unsurprising considering Wikipedia’s documented bias towards the pharmaceutical industry. Far more interesting is the institution that produced the research in the first place — the Salk Institute. The Salk Institute, named after Jonas Salk, the creator of the Salk polio vaccine, was constructed in 1962 thanks to funding from the National Foundation for Infantile Paralysis, today known as the March of the Dimes.

The March of the Dimes (MOD) was established in 1937 with the mission of eradicating polio and during a time when the Eugenics Establishment was already a prominent, but not yet popular, feature of the American health scene. The theory of Eugenics is based on the idea that selective procreation can lead to the gradual “improvement” of the human race and that certain families are fit to lead society by virtue of their “superior” genes.

At the time, the nation’s key eugenics organizations included the American Eugenics Society (AES) and the American Society of human Eugenics (ASHE), funded by the Rockefeller, Carnegie and Harriman families, as well as the Rockefeller Institute for Medical Research. It should be noted that the Rockefellers were instrumental in funding and promoting eugenics around the world. The Eugenics movement promoted selective mating, artificial insemination and compulsory sterilization and euthanasia as important means of weeding out so-called “inferior” human beings.

The first sterilization law in the US was passed in 1907, in the state of Indiana, and by 1931, many more states had followed suit by enacting similar laws. According to the Indiana Historical Bureau:

In 1907, Governor J. Frank Hanly approved first state eugenics law making sterilization mandatory for certain individuals in state custody.

Those sterilized under eugenics law were deemed “undesirable” on account of mental or physical impairments such as epilepsy, blindness and physical disabilities, as well as “social inadequacies” such as drug addiction or criminality. According to estimates, around 60,000 individuals were sterilized under such laws, deprived of their right to have children and forever branded as “feebleminded”.

In fact, the prominence of the American eugenics movement resulted in its adoption by the National Socialist Party of Germany, which sterilized more than 350,000 persons by the end of the second world war. After WW2, eugenics notions were dropped from public conversation, but the movement never dissipated, no, instead it was “re-branded” using more acceptable terminology such as “population control” and “reproductive health”, as we shall see later on.

The emergence of the MOD as a major player in the American Eugenics movement can be traced back to the organization’s early association with the Rockefeller Institute from where it procured many of its key members and advisers, including professor Anton Julius Carlson, a member of the American Eugenics Society, recruited to serve on the MOD’s Medical and Research Committees and Professor Clair E. Turner, another AES member who served as assistant to then President, Basil O’Connor.

Just before the establishment of the Salk Institute, the MOD announced it would be phasing out its polio programs and focusing its resources on “birth defects”. In 1959, the MOD funded courses in “medical genetics” at the Jackson Laboratory in Maine, a genetics institute founded in 1929 by Clarence Cook Little, who, “at one time or another” served as the president of the American Eugenics Society, the American Birth Control League and the American Euthanasia Society.

Jackson Laboratory’s claimed mission is “to discover precise genomic solutions for disease and empower the global biomedical community in its shared quest to improve human health.” Noteworthy is that the lab received increased funding in 2020, largely from the National Institute of Health (NIH), including a grant of $10.6 million to find treatments for rare genetic diseases by using gene-editing technologies. And at the start of the coronavirus “pandemic”, the lab worked to develop genetically modified mice for use in vaccine studies and other research related to Sars-Cov-2.

Beginning in the 1960s, the MOD financed several “Birth Defects Prevention Centers” located at medical institutions across the US. These new centers offered prenatal testing via amniocentesis to determine whether a baby would be born with “defects” and then gave the couple the opportunity to abort the affected child.

The MOD has also made direct donations to Planned Parenthood, a clear contradiction of their claimed mission, which is to “fight for the health of all moms and babies.” Planned Parenthood is a non-profit organization that provides “reproductive health care” in the US and abroad. From 2019-2020 the organization committed over 350,000 abortions and has been criticized as “steering resources away from women’s health and toward abortion.” Unsurprisingly, a look into the organization’s history reveals that Planned Parenthood has its roots in Eugenics ideals.

Planned Parenthood was founded by Margaret Sanger, who, far from a “birth control activist”, as the mainstream would have you believe, was a racist eugenicist who sought to rid the world of “unfit” human stock. In her essay, “A Plan for Peace”, she describes the main objects of her proposed “Population Congress” which includes “a stern and rigid policy of sterilization and segregation to that grade of population whose progeny is tainted, or whose inheritance is such that objectionable traits may be transmitted to offspring.” She also mentions the need to “control the intake and output of morons, mental defectives, epileptics.”

As mentioned earlier, these Eugenics ideals inspired the Nazis who took many of Sanger’s ideas and ran with them, so to speak. In his book, The War Against the Weak, Edwin Black details how the Nazi sterilization law of 1933 as well as subsequent euthanasia laws were based on blueprints drawn up by Sanger and other American “activists.” In fact, associates of Sanger knew about these Nazi euthanasia programs and praised them.

Coming back to the Salk Institute, it should be noted that the mainstream account of the 20th-century polio outbreak, namely the notion that the disease is caused by a virus and that Dr. Salk’s miracle vaccine was single-handedly responsible for ending the epidemic, is dubious and likely altogether false.

Paralytic polio appeared suddenly in the US in the early 1900s with continual, dramatic fluctuations in cases — a pattern that continued until the end of the 1950s. The introduction of the Salk vaccine in 1954 seemed to coincide with the almost instantaneous decline in cases, which continued for more than two decades.

But prior to being called “polio,” conditions involving infirmity of the limbs were known by various other names including apoplexy, palsy and paralysis. Many historical writings refer to paralysis resulting from exposure to toxic substances and many of these accounts were documented by Dr. Ralph Scobey in his 1952 statement to the Select Committee to Investigate the Use of Chemicals in Food Products titled The Poison Cause of Poliomyelitis and Obstructions to its Investigation.

Scobey’s paper includes references to several investigations that seemed to indicate a link between polio outbreaks in the 20th century and the consumption of fresh fruit, providing a link between Polio and toxic pesticide exposure. One crop pesticide in widespread use at the time was DDT, a highly toxic organochlorine that was widely publicized as being “good for you”, but eventually banned in 1972. In 1953, Dr. Morton Biskind published a paper in the American Journal of Digestive Diseases pointing out that “McCormick (78), Scobey (100-101), and Goddard (57), in detailed studies, have all pointed out that factors other than infective agents are certainly involved in the etiology of polio, varying from nutritional defects to a variety of poisons which affect the nervous system.”

The danger of toxic pesticides, including DDT, and their disastrous effects on the environment were illustrated by Rachel Carson in her 1962 book, Silent Spring.

In more recent times, researchers, Dan Olmstead, co-founder of the Age of Autism, and Mark Blaxil conducted two brilliant investigations into the polio epidemics of the 20th century, reaching a similar conclusion to Scobey and Biskind, namely that the disease was caused by the widespread use of neurotoxic pesticides such as arsenite of soda and DDT.

Although Salk’s vaccine was hailed as a success, the vaccine itself caused many cases of injury and paralysis. And though there does appear to be a convincing correlation between the timing of the vaccine and the reduction in polio cases, as all good scientists know, correlation doesn’t equal causation, especially considering the fact that DDT was phased out, at least in the US, over the same period.

Interestingly, Dr Salk’s polio research was funded by the mother of Cordelia Scaife May, an heiress to the Mellon family banking fortune who idealized Margaret Sanger and later joined the board of the International Planned Parenthood Foundation. May’s views on immigration were radical, to say the least, and according to some, she favoured compulsory sterilization as a means to limit birth rates in developing countries. May later joined the board of the Population Council, an organization founded by John D. Rockefeller III focused on population reduction. In 1995, the Population Council collaborated with the WHO to create fertility regulating vaccines.

It would be a mistake to think that the polio epidemic was not related to the current ‘age of vaccination’ we find ourselves in. On the contrary, claiming that polio was “eradicated in the United States” due to vaccination alone is a lie that garnered public favour for childhood vaccinations and helped to set the groundwork for the widespread belief in the safety and efficacy of all vaccines. Events such as Polio and Smallpox (another lie that is beyond the scope of this article), and the subsequent pro-vaccine propaganda, “primed” much of the population to accept, without question, an experimental jab based on poorly understood technology.

Twisting the Science

In 1997, 8 years after the Salk Institute paper, the FDA approved the first ever trial of transfected RNA to develop immunity in cancer patients. The Recombinant DNA Advisory Committee of the National Institute of Health then voted to continue approval some months later, leading to the first-ever mRNA based vaccine administered to humans.

Though mRNA is propagandized in the media as the next revolution in health, those with keen perception may be alarmed when reading excerpts such as this one, taken from an article on the history of mRNA, written by Damian Garde, a Biotech reporter for STATS:

The concept: By making precise tweaks to synthetic mRNA and injecting people with it, any cell in the body could be transformed into an on-demand drug factory.”

Talk of cells being turned into “on-demand drug factories” is exactly the sort of meaningless techno-rhetoric meant to impress and entice an uninformed public. mRNA vaccines are based on the following concept: a piece of synthetic mRNA is shuttled into your cells, where it is used as a template to create the viral “spike protein.” Once this protein leaves the cell, the body produces antibodies and “learns” how to fight future Sars-Cov-2 infections.

mRNA-based vaccines are often touted as a safer alternative to DNA-based vaccines, which, according to researcher Steve Pascolo “may trigger permanent and dangerous changes in the genetic information of treated people”. However, do we know for sure that mRNA vaccines don’t permanently change the genetic makeup of our cells? A 2001 paper titled “RNA as a tumor vaccine: a review of the literature< " states that (emphasis added): “unlike DNA-based vaccines, there is little danger of incorporation of RNA sequences into the host genome.” The use of the word “little” would seem to indicate that there may be at least some danger of genome integration or more likely, researchers simply don’t know.

In the 2004 “expert opinion” paper by Pascolo cited above, he outlines the link between mRNA vaccines and gene therapies, something which is continually denied and dismissed by the mainstream:
A

lthough located in the cytosol and not in the nucleus, mature mRNAs belong to the biochemical family of nucleic acids. mRNA, similarly to DNA, may be considered a gene and, consequently, it’s use as a vaccine may be viewed as ‘gene therapy’.

Interestingly, it is purely due to a technicality of regulatory law that covid-19 gene therapies are allowed to be called “vaccines”. This is explained in a paper titled “The European Regulatory Environment of RNA-Based Vaccines,” which states that:

The definition of a gene therapy medicinal product as outlined in Annex 1 to Directive 2001/83/EC is as follows:

Gene therapy medicinal product means a biological medicinal product which has the following characteristics:

(a) it contains an active substance which contains or consists of a recombinant nucleic acid used in or administered to human beings with a view to regulating, repairing, replacing, adding or deleting a genetic sequence;

(b) its therapeutic, prophylactic or diagnostic effect relates directly to the recombinant nucleic acid sequence it contains, or to the product of genetic expression of this sequence.

Gene therapy medicinal products shall not include vaccines against infectious diseases.

As is evident, the mere act of calling a gene therapy a “vaccine against infectious disease” negates its classification as a gene therapy, the approval process for which, at least in Europe, involves going through the CAT which is the EMA’s (European Medicines Agency) “Committee for Advanced Therapies”. Evidently, this play on language would seem to constitute a “loophole” of sorts, allowing easier approval for mRNA based gene therapies planned for human use.

Approval is certainly a contentious topic when talked about in the context of the current covid-19 vaccines, none of which have been fully FDA approved, only authorized under emergency use (EUA) and labeled as “investigational” products, a fact that many people are unaware of. However, early in the year vaccine manufacturers already set their sights on full regulatory approval, after only 6 months of trial data. On the 7th of May, Pfizer formally initiated their application to the FDA, with the aim of having the first-ever fully approved covid-19 vaccine. But with millions of vaccines already administered under EUA, what’s the rush?

Furthermore, for the six “first in disease” vaccines approved by the FDA over the last 15 years, the median trial duration was just shy of two years. A vaccine approved after 6 months of data would constitute one of the fastest ever. The phase three clinical trials for Pfizer, Moderna and Janssen are two years in duration, but the FDA has not clearly stated their position with regards to minimum follow-up prior to consideration for approval.

Longer, placebo-controlled trials are paramount to assessing vaccine safety. It is extremely alarming then that vaccine manufacturers, within weeks of receiving EUA, began to unblind trials by offering those in the placebo group the chance to get vaccinated. Moderna announced that “as of April 13, all placebo participants have been offered the Moderna covid-19 vaccine and 98% of those have received the vaccine,” meaning that their placebo group no longer exists and as such, they have no way to accurately measure long-term safety.

In an article for the British Medical Journal, Peter Doshi quotes the FDA, on several occasions, saying that the maintenance of a placebo group would be critical to assessing both the safety and efficacy of covid-19 vaccines, which is obvious to anyone who understands the consequences of failing to adhere to scientific rigor when testing a new medical therapy.

In reality, there could be many reasons for manufacturers wanting FDA approval for their vaccines, but likely top of the list is the “stamp of approval” that comes with full licensure and the ability to use this as a way to convince those who remain skeptical regarding the safety and efficacy of the vaccines. Moreover, full FDA approval would pave the way for easier vaccine mandates, putting immense pressure on those of the “awakened class” who represent a thorn in the side of the Great Reset/Great Convergence agenda pushers.

More disturbing inconsistencies can be found in the FDA’s process for assessing and approving these experimental vaccines. For example, the FDA recently cautioned against the use of antibody tests for evaluating immunity or protection from covid-19, “especially” after a person has received a vaccination, despite their EUA being originally granted, in part, due to antibody responses. The implication for this reversal is that the EUA given for covid-19 vaccines should also be reversed, but what’s the likelihood of that happening, after millions have already been jabbed?

Moreover, the idea that “antibodies” provide protection from so-called viral infections represents a poor understanding of the body and the immune system. The fact that antibodies play little role in viral infections has been known by medical scientists since the 1950s based on research that shows persons with the genetic inability to produce antibodies, called “agammaglobulinemia,” have normal reactions to typical viral infections and even appear to resist recurrences.

Bill Gates, Moderna, and Eugenics 2.0

One of the covid-19 vaccine manufactures most talked about in the media is Moderna, a biotech company co-founded by Robert Langer, a researcher and inventor at MIT. In 2013, the biotech startup received $25m in funding from DARPA (the Defense Advanced Research Projects Agency), a research arm of the United States Department of Defense, and an organization well-known for ruthlessly pursuing dystopian, transhumanist technologies, such as implantable nanoparticles and bio-brain interfaces (more on this later).

Noteworthy is that the US government, through the National Institute of Health, appears to have a financial stake in the Moderna vaccine thanks to a contract signed by both parties, giving the NIH joint ownership over Moderna’s mRNA vaccine candidates. According to Axios:

The NIH mostly funds outside research, but it also often invents basic scientific technologies that are later licensed out and incorporated into drugs that are sold at massive profits.

This is more than alarming considering the NIH is responsible for prioritizing promising treatments for covid-19 as well as improving clinical trial effectiveness, which, for Moderna, is impossible considering their trial no longer contains a control group. NIH’s vested interest in Moderna’s success may also provide a plausible explanation for why the biotech startup received EUA for their vaccine despite failing, for over 10 years, to bring a single product to market.

In an interview for Economic Club, NIH director Francis Collins denied that covid-19 vaccines would be money-makers, saying that “Nobody sees this as a way to make billions of dollars”. However, evidence points to the contrary as Moderna’s covid-19 vaccine sales reached $1.7 billion in the first quarter of 2021, making their CEO, Stephane Bancel, one of the many new pharma billionaires.

“Operation Warp Speed,” the name given to a partnership between several US Federal agencies aimed at accelerating the development of a covid-19 vaccine, was also wrought with conflicts of interest. The Operation Warp Speed administration hired several “consultants” with ties to Big Pharma, including two former Pfizer executives. And in May 2020, it was reported that their chief adviser, Dr. Monsef Slaoui, a former pharmaceutical executive himself, held $10m in GlaxoSmithKline stock, the same company that was later awarded a $2 billion contract to supply the US government with 100 million vials of covid-19 vaccine. Dr. Slaoui also held significant stock in Moderna, to whom the federal government has awarded over $2.5b in funding.

Moderna co-founder, Robert Langer, whose net worth has also skyrocketed into the billions, is one of the world’s most cited researchers. A scientist at MIT, Langer holds over 1,400 patents and specializes in biotechnology, nanotechnology, tissue engineering and drug delivery. Furthermore, Langer holds an administrative role at the MIT Media Lab, the same institute that was the focus of a scandal after it was revealed that the lab accepted funding from convicted sex-offender, Jefferey Epstein. Epstein also happened to have a disturbing fascination with “transhumanism”, a modern-day version of eugenics (transhumanism is discussed later in this article).

Then director of the MIT Media Lab, Joi Ito, approved two donations from Epstein of $1.75m and allowed the prolific paedophile to “direct” funds to the lab from other wealthy benefactors, including a $2m donation from Bill Gates, who also has unsettling ties to Epstein, having flown on his private jet and met with him on several occasions. When the news broke out and Joi Ito resigned from his post at the lab, Langer was one of the first people to sign a letter calling for him to stay, and as an administrator for the lab’s Director’s Office, it’s hard to believe he didn’t know about the Epstein donations in advance.

Described as the “common denominator” in several coronavirus efforts, Robert Langer is certainly an interesting player in the transhumanist movement. In 2015, his company, Microchips Biotech, partnered with Israeli pharmaceutical giant, Teva Pharmaceutical, to commercialize its “implantable drug delivery device”. Noteworthy is that Teva Pharmaceutical has received significant investment from Warren Buffett, who, in 2006, pledged to gradually donate his fortune to the Bill & Melinda Gates Foundation, an organization whom he served as a trustee up until very recently.

Langer also has ties to Charles Lieber, a Harvard nanotech scientist who was arrested in January on account of making false statements to federal authorities regarding his collaboration with Chinese researchers at the Wuhan University of Technology. In 2012, Langer and Lieber worked together to create a “material that merges nanoscale electronics with biological tissues”. The material was described as “a first step toward prosthetics that communicate directly with the nervous system”.

Much of Langer’s research is backed by Bill Gates, who began funding mRNA technology in 2010 and has also invested millions into Moderna. In 2017, the Bill and Melinda Gates Foundation sponsored a project at Langer’s lab to create a microparticle vaccine delivery system that could generate a “novel type of drug carrying particle”, allowing multiple doses of a vaccine to be administered over an extended period of time with just one injection. Then in 2019, Gates and Langer teamed up again to create an invisible ink tattoo that “embeds immunization records into a child’s skin”. Disturbingly, the eventual goal of the project is to inject sensors that can be used to track “other aspects” of health.

Gates claims he needs the data for “disease prevention”, referring to his efforts to wipe out polio, measles and other “infectious” diseases from around the world. However, Gates’ various “health-related” initiatives in developing countries are not the work of a loving philanthropist like the media would have us all believe. Instead, evidence would suggest that Gates’ involvement in public health represents the continuation of a long-standing eugenics agenda, hiding in plain sight. Gates’ links to the eugenics movement start with his father, who praised the Rockefellers for their work in “public health” and even met with them in 2000 to discuss matters relating to infectious disease, vaccines and the environment. During the meeting, Gates senior was quoted as saying:

Taking our lead and our inspiration from work already done by The Rockefeller Foundation, our foundation actually started GAVI by pledging $750 million to something called the Global Fund for Children’s Vaccines, an instrument of GAVI.

Interestingly, almost ten years after that meeting, Gates junior co-hosted a meeting with David Rockefeller to discuss population reduction.

Perhaps even more telling is the fact that in 2012 Bill and Melinda Gates hosted their London Summit on Family Planning, where they announced their commitment to population control in the third world, on the 100th anniversary of the First International Eugenics Congress, also held in London.

Gates is well-known for his obsession with vaccines, a curious pursuit considering that the 9,000,000 people who die every year from hunger would be better served by having clean water, food supplies and sanitary living environments. In 2009, Gates’ Foundation funded observational studies in India for a controversial cervical cancer vaccine that was given to thousands of young girls called “Gardasil”. Within months, many girls began to get sick and within a year, five of them had died. During a similar study for a different brand of HPV vaccine, many girls were hospitalized and a further two died. The Economic Times of India reported on this in 2014, with the shocking revelation that:

Consent for conducting these studies, in many cases, was taken from the hostel wardens, which was a flagrant violation of norms. In many other cases, thumbprint impressions of their poor and illiterate parents were duly affixed onto the consent form. The children also had no idea about the nature of the disease or the vaccine. The authorities concerned could not furnish requisite consent forms for the vaccinated children in a huge number of cases.

Gates has also heavily promoted the oral polio vaccine in India, after endeavouring to eradicate the disease. However, as discussed earlier in this article, toxic chemicals are involved in the etiology of polio and thus the disease cannot be eradicated by the use of vaccines. In fact, global health numbers indicate that more cases of polio are now being caused by the vaccines themselves than anything else. In 2018, a group of brave Indian researchers published a paper in the International Journal of Environmental Research and Public Health showing a correlation between the oral polio vaccine drives and increased cases of “acute flaccid paralysis”, a condition described as “clinically indistinguishable” from polio.

Ironically, Gates has a $23m investment in Monsanto, the company that markets “roundup” a glyphosate-containing pesticide that is known to cause adverse health effects, including neurological disorders and paralysis.

While many believe Gates to be selflessly giving away his money in order to fund these vaccination campaigns, it should be noted that Gates’ investment in vaccines has netted him a massive return. By 2019, the Bill and Melinda Gates Foundation had donated just over $10b to various vaccine-related initiatives including GAVI (the Global Alliance for Vaccines and Immunization). Gates called it the “best investment he’s ever made”, estimating a 20-1 return, or around $200b over 20 years. Indeed, Gates’ net worth has more than doubled over the last 10 years.

And lest we forget that more than half of all deaths in low to middle income countries are caused by non-communicable diseases, which the Bill and Melinda Foundation seems to have little interest in, directing less than 3% of their budget towards such conditions.

Furthermore, Gates’ activities in public health are wrought with conflicts of interest that that would seem to undermine the notion that Gates cares about the health of the population. Many of these conflicts of interest are outlined in a study published by Harvard researcher, David Stuckler, titled “Global Health Philanthropy and Institutional Relationships: How Should Conflicts of Interest Be Addressed?,” in which he states that:

As one example, we found that Bill & Melinda Gates Foundation has substantial holdings in the Coca-Cola Corporation, and also participates in grants that encourage communities in developing countries to become business affiliates of Coca-Cola. It has been noted by some commentators that sugary drinks such as those produced by Coca-Cola are correlated with the rapid increase in obesity and diabetes in developing countries.

Stuckler also notes that:

Many of the Foundation’s pharmaceutical development grants may benefit leading pharmaceutical companies such as Merck and GlaxoSmithKline.” And that “Several grants are linked to companies that are represented on the Foundation’s board among its investments.

The media rarely reports on these disturbing conflicts of interest, which isn’t surprising considering Gates funds all the major news outlets.

To call the negligent, wide-spread administration of covid-19 experimental vaccines an initiative steeped in eugenicist thinking would not be amiss considering how many figures and institutions involved in the vaccine race have ties to the eugenics movement. In fact, the developers of the Oxford-AstraZeneca vaccine are also linked to the now renamed British Eugenics Society, founded by the father of Eugenics, Francis Galton. These connections are detailed by investigative journalist, Whitney Webb, in her article titled “Developers of Oxford-AstraZeneca Vaccine Tied to UK Eugenics Movement.”

When it comes to protecting public health, the recklessness displayed by politicians, scientists and pharmaceutical companies is unforgivable considering the widespread impact that these experimental vaccines will have. We have already begun to see the results of unleashing a dangerous gene therapy technology on a naive and trusting public, with VAERS, (the Vaccine Adverse Events Reporting System) showing more deaths linked with covid-19 vaccines than all other vaccines combined over the last 30 years.

None of this is surprising though, considering the haste with which clinical trials were conducted and the question marks surrounding the reliability of the data reported. For example, vaccine manufactures reported their vaccines were “95% effective”, a number they arrived at by using a relative risk reduction as opposed to an absolute risk reduction, which was around 1% in most cases, a fact never highlighted by the mainstream media.

Furthermore, vaccine trials were not designed to assess the vaccines’ effect on infection, transmission, hospitalizations or deaths, which is puzzling considering that, if there really was a viral pandemic, these would be the most important endpoints to test for. Though perhaps this was a calculated move by vaccine manufacturers, who knew they’d have a better chance at rigging the results using the endpoint of ‘covid-19 of any severity’. After all, the dramatic increase in the use of influenza vaccines has not been associated with a decrease in mortality.

Peter Doshi, an editor for the British Medical Journal, has called into question numerous aspects of the controversial vaccine trials, including the potential for pain medication to mask covid-19 symptoms in trial groups and the objectivity of “primary event adjudication committees” in charge of counting covid-19 cases. In the case of Pfizer, this committee consisted of Pfizer employees.

Recently, Doctors for Covid Ethics, a group consisting of Dr. Michael palmer MD, Dr. Sucharit Bhakdi MD and Dr. Stefan Hockertz PhD, published an expert statement relating to the danger and efficacy of the Pfizer vaccine that was submitted as part of a lawsuit challenging the EU’s authorization of the use of the vaccine for children 12 years and older. The paper states that the reported efficacy of the Pfizer mRNA vaccine was “most likely altogether fraudulent” and that “Pfizer, the EMA, and the FDA have systematically neglected evidence from preclinical animal trials that clearly pointed to grave dangers of adverse events.”

But of course, none of this is ever surfaced in the mainstream. Instead, we are fed the same party lines over and over; “vaccines are safe and effective,” “follow the science,” “listen to the experts.” And by “experts” they of course mean the pharmaceutical reps like Dr. Anthony Fauci, the director of the U.S. National Institute of Allergy and Infectious Diseases whose been lying about so-called viral infections ever since AIDS broke out in 1984. The fact that a character like Fauci has held his post for more than 30 years is rather telling of how the system works. The late Nobel prize winner and inventor of Polymerase Chain Reaction (PCR), Karry Mullis, castigated Fauci in an interview, saying that:

He doesn’t know anything really about anything, and I’d say that to his face. Nothing.

The man thinks you can take a blood sample and stick it in an electron microscope and if it’s got a virus in there, you will know it. He doesn’t understand electron microscopy and he doesn’t understand medicine. He should not be in a position like he’s in […] Tony Fauci does not mind going on television in front of the people who pay his salary and lie directly into the camera.

A Transhumanist Future

Besides being gene therapies, a technology associated with eugenics and transhumanism, according to scientists, mRNA technology “allows rapid development of novel vaccines within a very short time span of weeks rather than months.” Hence, we may be faced with the possibility of a future filled with on-demand vaccines created to “protect” the public against new, invisible threats.

Indeed, with vaccinologists already talking about “variants”, booster shots and periodic covid-19 top-up vaccines, it certainly looks like things are headed that way. And of course, thanks to intelligence-linked Big Tech conglomerates, this data will all be recorded on a “vaccine passport” linked to your smartphone, which will no-doubt form the basis for a new type of digital identity pass tied to your bank account and, eventually, your social credit.

Indeed, in 2019, Bill Gates’ Microsoft filed a patent, aptly named Patent WO2020060606, for a “Cryptocurrency system using body-activation data,” another clue as to the true intentions of the technocratic elite who are funding and promoting the transhumanist agenda. The patent’s title alone conjures up images of a slave society in which humans are fitted with biosensors and awarded digital coins for completing tasks issued to them by the ruling elite.

But perhaps even more alarming is the rush to get gene therapies licensed for use in young children. Pfizer are currently in the midst of a global clinical trial, where they are testing their mRNA jabs in babies as young as 6 months, despite the fact that “Covid-19”, if we suppose there is such a disease, barely affects children. In fact, according to CDC numbers, the IFR in children is 20 per 1,000,000, or 0.002%, which is likely lower than the risk of permanent injury or death from the MMR vaccine. It’s also lower than the covid-19 vaccine death rate as calculated using VAERS data at the time of writing (5,612 deaths over 165,000,000 fully vaccinated in the US = 0.003%). Furthermore, research has linked Pfizer’s vaccine to symptomatic myocarditis, with an estimated incidence rate of 1 in 3000 or 1 in 6000 in young men.

The rush to bring mRNA vaccines into the mainstream as part of the regular childhood vaccination schedule is not about health or protection, but rather a step towards a much more sinister goal, which is to attain control over the human body itself.

As mentioned previously in this article, DARPA, the research arm of the US Department of Defense, has been working to create nanotechnology that can interface with biological cells. In 2014, DARPA launched its “In Vivo Nanoplatforms (IVN)” program, with the aim of developing implantable nanoplatforms to collect biological data and provide “continuous physiologic monitoring”. The program has since helped to create injectable hydrogels that monitor physiologic responses and can sync to a smartphone.

Furthermore, DARPA, together with the NIH, heavily funds Profusa, a Google-backed biotech company developing and marketing this very same injectable hydrogel technology, only now it is being punted as a way to detect future “pandemics”. Allegedly, Profusa’s sensors can “detect flu-like infections even before their symptoms begin to show”. While incredibly disturbing, this is only a step towards DARPA’s ultimate goal, which is to establish dominion over the mind. This goal is reflected in DARPA’s research to create “mutant-powered soldiers” using “genetic weaponry” that can “undermine people’s minds and bodies using a range of chemical, neurological, genetic and behavioral techniques”.

DARPA is also looking at ways to genetically engineer the brain in order to read peoples thoughts and induce images and sounds in people’s minds. The research involves the use of “magnetic nanoparticles”, the same technology that some have speculated may be included in current or future covid-19 vaccines.

Equally distressing is the “Wellcome Leap”, a new initiative created by the eugenics-linked Wellcome Trust, the world’s richest medical research Foundation, in partnership with two former DARPA frontmen. The program’s official aim is to “Deliver breakthroughs in human health over 5 – 10 years and demonstrate seemingly impossible results on seemingly impossible timelines.” Currently, the initiative has 5 main projects, the first of which is “RNA Readiness + Response”, which seeks to (emphasis added) “create a self-sustaining network of manufacturing facilities providing globally distributed, state-of-the-art surge capacity to meet future pandemic needs”, referring to the manufacturing of RNA-based products (mRNA gene therapies). Note the seeming surety of a future pandemic.

However, the top contender for most disturbing Wellcome Leap project is, without a doubt, “The First 1000 days” (1kD), a program which seeks to use infants as test subjects in order to monitor their brain development and create AI models that can be used to “accurately predict and improve EF [executive function] outcomes.” The project also notes the use of “mobile-sensors, wearables and home-based systems.” In a detailed article on the matter, researcher Whitney Webb writes that:

True to the eugenicist ties of the Wellcome Trust (to be explored more in-depth in Part 2), Wellcome Leap’s 1DK notes that “of interest are improvements from underdeveloped EF to normative or from normative to well-developed EF across the population to deliver the broadest impact.” One of the goals of 1DK is thus not treating disease or addressing a “global health public challenge” but instead experimenting on the cognitive augmentation of children using means developed by AI algorithms and invasive surveillance-based technology.

The Wellcome Leap’s timeline of 5-10 years happens to line up with elite frontman, Elon Musk’s Neuralink project, which seeks to establish “the future of brain interfaces” in order to “expand our abilities”. In an interview Musk said, “I think we are about 8 to 10 years away from this being usable by people with no disability”. Musk, whose wealth increased by more than 500% during the covid-19 “pandemic”, founded Neuralink in 2016. The company recently raised $205m in funding from 7 venture capital firms (including Google’s GV) and 5 Silicon Valley executives. However, Neuralink isn’t the only biotech company pursuing this technology. Recently, Synchron, a small biotech firm and Neuralink competitor, received the go-ahead from the FDA to begin testing its brain chip implants in humans.

10 years from now would take us to 2030, a year that comes up again and again as a year in which transhumanist technologies will be commonplace in mainstream society. According to predictions made by the US National Intelligence Council, “human augmentation” (the merging of man and machine) will be a major theme in 2030. Their Global Trends 2030 report, published in 2012, states that:

Successful prosthetics probably will be directly integrated with the user’s body. Brain-machine interfaces could provide “superhuman” abilities, enhancing strength and speed, as well as providing functions not previously available.

Interestingly, the report also predicts “an easily transmissible novel respiratory pathogen” that could cause a great disruptive impact. The report goes on to state that “Unlike other disruptive global events, such an outbreak would result in a global pandemic that directly causes suffering and death in every corner of the world, probably in less than six months.”

Enslavement: A Free Will Choice

The rollout of mRNA gene therapies and the push towards a transhumanist society represents the continuation of the eugenics movement, which was based on the pseudoscientific concept that some humans, by virtue of their genetic composition, were more “fit” to lead society than others.

The “hero” of the Polio epidemic, Jonas Salk, had his own ties to eugenics and so does the institute named in his favour, the Salk Institute. Their mRNA research, funded by the NIH, set the foundation for the development and mass rollout of gene therapies, controversially being called “vaccines”. The danger of this experimental technology is evident, having already caused thousands of injuries and deaths worldwide.

The role of intelligence organizations, billionaire technocrats and pharmaceutical initiatives in funding, researching and promoting mRNA vaccines, “bio-brain” interfaces, gene editing and other technologies steeped in eugenicist ideals paints the picture of a global agenda set to hit its stride fully by 2030. The current covid-19 “pandemic” has served as a means to accelerate this agenda by centralizing wealth and power, bringing transhumanist technology into the mainstream and normalizing authoritarian rule. Pfizer’s infant trials and the Wellcome Leap’s alarming “1kD” project indicate that key to this agenda is the conditioning and control of children from a young age, something that Aldous Huxley detailed extensively in his disturbingly prophetic, eugenicist novel, Brave New World.

This agenda, though backed by some of the world’s most powerful individuals and institutions, has an obvious weakness — its success is reliant on our compliance. It will only advance if we allow it to advance. Therefore, it is up to each one of us, through compassionate, non-violent resistance, to sow the seeds of awakening in the collective consciousness of mankind.

The post mRNA “Vaccines,” Eugenics, and the Push for Transhumanism first appeared on Dissident Voice.

Vaccine Billionaires and Human Guinea Pigs

How do you make a potentially dangerous and ineffective drug appear like a miracle of modern science? You could, for instance, enrol only certain people in clinical trials and exclude others or bring the study to a close as soon as you see a spike in the data that implies evidence of effectiveness.

There are many ways to do it.

According to health practitioner and writer Craig Stellpflug in his article ‘Big Pharma: Getting away with murder’ (2012), the strategy is to get in quick, design the study to get the result you want, get out fast and make lots of money.

Stellpflug says:

If a study comes up negative for your favorite drug, just don’t publish it! 68 per cent of all drug studies are swept under the carpet to keep those pesky side effects from being reported. Only 32 per cent of studies come up positive and a lot of those studies are ‘shortened’ to limit the long-term findings. Studies cut short were found to overestimate the study drug’s effectiveness and miss dangerous side effects and complications by an average of 30 per cent. This would explain the amazing 85 per cent drug study success rate in the hands of Big Pharma according to the Annals of Internal Medicine.

Of course, it helps to get the regulatory agencies on board and to convince the media and health officials of the need for your wonder product and its efficacy and safety. In the process, well-paid career scientists and ‘science’ effectively become shaped and led by corporate profit margins and political processes.

And what better way to make a financial killing than by making a mountain out of a molehill and calling it a ‘pandemic’?

COVID-19 vaccine concerns

The Wall Street Journal recently published an article by two health professors who said politics — not science — is behind the failure of health officials and the media to fully inform the public about the potential risks associated with COVID vaccines.

Although the article is available in full to subscribers only, the Children’s Health Defense (CHD) website provides an informative summary.

The CHD notes that Dr Joseph A Ladapo, associate professor of medicine at the David Geffen School of Medicine, and Dr Harvey A Risch, professor of epidemiology at Yale School of Public Health, wrote that while prominent scientists have raised concerns that the safety risks of Covid-19 vaccines have been underestimated, the politics of vaccination has relegated their concerns to the outskirts of scientific thinking.

The two professors noted that clinical studies do not always tell the full story about the safety of medications and that the health effects often remain unknown until the medicine is rolled out to the general public. Examples include Vioxx, a pain reliever that increased the risk of heart attack and stroke; antidepressants that appeared to increase suicide attempts among young adults; and an influenza vaccine used in the 2009-10 swine flu epidemic that was suspected of causing febrile convulsions and narcolepsy in children.

The authors added that clinical trials often enroll patients who are not representative of the general population and more is learnt about drug safety from real-world evidence. With this in mind, they said the large clustering of side effects following COVID vaccines is concerning as is the silence around these potential signals of harm.

Serious adverse events reported by the Vaccine Adverse Event Reporting System include low platelets, heart inflammation, deep-vein thrombosis and death. However, the two scientists argue this is likely to be a fraction of the total number of adverse events.

They criticise the Centers for Disease Control and Prevention (CDC) and the US Food and Drug Administration (FDA) for ignoring the reported serious COVID vaccine side effects.

The authors acknowledge the risks of COVID vaccines in certain populations, not least children, may outweigh the benefits. They also state that not a single published study has demonstrated that patients with a prior infection benefit from COVID-19 vaccination. Something which is not readily acknowledged by the CDC or Anthony Fauci, an indication, according to the authors, of how deeply entangled pandemic politics is in science.

They conclude that public health authorities are making a mistake and risking public erosion of trust by not being forthcoming about the possibility of harm from the vaccines.

Merck and Vioxx

It is revealing that the two scientists refer to Vioxx, which was once popular for treating the symptoms of arthritis. It was removed from the market in 2004 after concerns that it may have injured hundreds of thousands of patients, while possibly killing tens of thousands in the US.

Dr David Graham, whistleblower and senior FDA investigator, criticised the FDA’s approval process of Vioxx (rofecoxib), an anti-inflammatory drug administered orally. In various interviews and congressional hearings, he described the outcome of Vioxx as disastrous and unparalleled in the history of the US. He added that the saga surrounding Vioxx had constituted an unprecedented failure of the nation’s system of drug approval and oversight.

In 2004, Graham argued that the painkiller had caused 88,000 to 139,000 heart attacks in the US – 30-40 per cent of which were fatal – over the previous five years. Nevertheless, manufactured by Monsanto (a company with a proven track record of corrupt practices) and co-marketed by Merck, Vioxx became a leading drug in providing pain relief from the symptoms of various forms of arthritis.

Research presented to the FDA in early 2001 showed that patients taking Vioxx had a higher risk of heart attack compared to those taking some of the older alternatives.

However, the real game-changer came in 2004 when Dr Graham released the findings that found Vioxx increased the chance of heart attack and death from cardiac arrest significantly more than its biggest rival on the market. Dosages of Vioxx in excess of the recommended daily dose of 25 milligrams were also found to more than triple a patient’s risk compared to those who had not taken painkillers.

In September 2004, Vioxx was pulled from the market. But in 2006, more damning findings were revealed by a study that showed that some patients had likely suffered from a heart attack much sooner after starting treatment with Vioxx. Appearing in the Canadian Medical Association Journal, the study showed that 25 per cent of the patients who had heart attacks while taking Vioxx did so within two weeks of starting the drug. This indicated that Vioxx-related cardiovascular risks may occur much earlier than previously thought.

The FDA was criticised for its close relationship with Merck and witnesses at a senate finance committee hearing described how danger signals of Vioxx went ignored. Indeed, a 2007 article published by the National Institutes of Health alleged that even though scientists at Merck knew that the drug might adversely affect the cardiovascular system, none of the intervention studies submitted to the FDA in 1998 were designed to evaluate such risk.

Robber barons and guinea pigs

Merck reported over $11 billion in Vioxx sales during the five years the drug was on the market. To date, the company has paid nearly $6 billion in litigation settlements and criminal fines over Vioxx. Still, in hard-nosed commercial terms, it was a massive success, resulting in a $5 billion gain for the company.

In May 2021, it was reported that Covid-19 vaccines had created at least nine new billionaires. According to research by the People’s Vaccine Alliance, the new billionaires included Moderna CEO Stéphane Bancel and Ugur Sahin, the CEO of BioNTech, which has produced a vaccine with Pfizer. Both CEOs were then worth around $4 billion. Senior executives from China’s CanSino Biologics and early investors in Moderna have also become billionaires.

Although the nine new billionaires are worth a combined $19.3 billion, the vaccines were largely funded by public money. For instance, according to a May 2021 report by CNN, BioNTech received €325 million from the German government for the development of the vaccine. The company made a net profit of €1.1 billion in the first three months of the year, largely thanks to its share of sales from the Covid-19 vaccine, compared with a loss of €53.4 million for the same period last year.

Moderna’s Covid-19 vaccine sales reached $1.7 billion in the first three months of this year and it had its first profitable quarter ever. Moderna is expected to make $13.2 billion in Covid-19 vaccine revenue in 2021. The company received billions of dollars in funding from the US government for development of its vaccine.

Big Pharma has every reason to perpetuate the notion of a deadly global pandemic and to inflate the efficacy of and need for its vaccines. And it, along with its associates in government and at the WHO, has every reason to discredit alternative and arguably more effective treatments like Ivermectin (see the online article ‘The Campaign against Ivermectin: WHO’s Chief Scientist Served with Legal Notice for Disinformation and Suppression of Evidence‘).

There is no need to cover ground here that has been covered extensively elsewhere but it is now abundantly clear that many continue to question the overall official COVID-19 narrative, the fear propaganda, the specific data, the PCR testing protocols, the apparent conflicts of interest and vaccine efficacy.

Moreover, a group of 57 leading scientists, doctors and policy experts recently released a report calling in to question the safety and efficacy of the current Covid-19 vaccines. They are calling for an immediate end to all vaccine programmes.

There are hundreds of scientists who have questioned government and WHO strategy and who have brought attention to the extremely low risks posed by COVID to the bulk of the population as well as the destructive (ineffective) policies and decisions pertaining to lockdowns and other restrictions.

There are many other top scientists who are questioning the need for mass vaccination and who have also pointed out credible and extremely disturbing side effects (real and potential) of such a strategy, not least Dr Robert Malone, credited with developing mRNA vaccine technology, Dr Byram Bridle, a viral immunologist, and Dr Geert Vanden Bossche, a prominent virologist and vaccine expert.

Unlike Merck and Vioxx, it will be governments (the public) that foot any future indemnity costs of these experimental vaccines that have escaped proper (long-term) testing. And given the scale of the rollout, the damage caused could make the adverse effects of Vioxx seem a mere blip.

Vaccines that were brought to market via emergency authorisation use for an ‘emergency’ constructed on the basis of deaths so often wrongly attributed to COVID-19.  Brought to market on the basis of flawed PCR test protocols with magnification cycles primed to create a ‘casedemic’.

To borrow from Dr David Graham: are we currently witnessing something more disastrous and unparalleled in the history of the world, let alone the US: an unprecedented failure of global drug approval and oversight?

In the meantime, while billions of vaccinated people serve as human guinea pigs, the newly crowned vaccine kings will make hay while the sun shines (and the fear continues).

The post Vaccine Billionaires and Human Guinea Pigs first appeared on Dissident Voice.

The Vaccine Must Be a Common Good for Humanity

Vladimir Griuntal’ and G. Iablonovskii (USSR), Chto eto takoe? (‘What is This?’) 1932.

Vladimir Griuntal’ and G. Iablonovskii (USSR), Chto eto takoe? (‘What is This?’) 1932.

Nearly three million people have reportedly been killed by the novel coronavirus (SAR-CoV-2) and upwards of 128 million people have been infected by the virus, many with long-lasting health repercussions. Thus far, roughly 1.5% of the world’s population of 7.7 billion have been vaccinated, but 80% of them are from only ten countries. In February, Tricontinental: Institute for Social Research warned about the ‘medical apartheid’ that has shaped the vaccine roll-out.

Since 1950, the World Health Organisation (WHO) has celebrated Global Health Day on 7 April. Each year, the WHO choses a different theme for the day, with last year’s being ‘Support Nurses and Midwives’. This year, the theme is ‘Building a fairer, healthier world’, which goes to the heart of medical apartheid.

On 1 April, the International Week of Anti-Imperialist Struggle released the ‘International Manifesto for Life,’ which called for ‘free vaccines for all people’. This week’s newsletter is dedicated to our Red Alert no. 10, which – with the guidance of scientists and doctors – looks at the need for a people’s vaccine.

What is a vaccine?

Infectious diseases can cause serious illness and death. Those who survive the infection often develop long-lasting protection from that same disease. About 150 years ago, scientists discovered that infections are caused by microscopic ‘germs’ (what we now call pathogens), which can spread from animals to humans and from person to person. Could a small or weakened portion of these pathogens trigger changes in the body that might protect people from severe infections in the future? This is the principle behind vaccines.

A vaccine, containing microscopic molecules that mimic parts of an infection pathogen, can be injected into the body to activate this pre-emptive protection against the disease. Although one vaccine protects just one individual against just one pathogen, when many vaccines are considered together in organised, large-scale vaccination programmes, they become crucial to community-level interventions.

Not all infections can be prevented by vaccines. Despite huge financial investments, we still do not yet have (and may never have) dependable vaccines for certain infectious diseases – such as HIV-AIDS and malaria – due to these diseases’ biological complexity. It has been possible for COVID-19 vaccines to be rushed into use because – for the most part– they are based on well-understood biological mechanisms in less complex disease situations. Vaccines are an important measure to contain infectious epidemics. However, genetic changes in the infectious microbe can make vaccines ineffective and necessitate development and deployment of new vaccines.

Roger Melis (DDR), Kinder in der Kollwitzstraße (‘Children in Kollwitzstraße’), 1974.

Roger Melis (DDR), Kinder in der Kollwitzstraße (‘Children in Kollwitzstraße’), 1974.

Why aren’t COVID-19 vaccines being provided to all of the world’s 7.7 billion people?

Not long after the emergence of the novel coronavirus (SAR-CoV-2), Chinese authorities sequenced the virus and shared that information on a public website. Scientists from public and private institutions rushed to download the information to better understand the virus and to find a way to both treat its effects on the human body and to create a vaccine to immunise people against the disease. At this stage, no patent was issued on any of the information.

Within months, eight private and public sector firms announced that they had vaccine candidates: Pfizer/BioNTech, Moderna, AstraZeneca, Novavax, Johnson & Johnson, Sanofi/GSK, Sinovac, Sinopharm and Gamaleya. The Sinovac, Sinopharm, and Gamaleya vaccines are produced by the Chinese and Russian public sectors (by mid-March, China and Russia had provided 800 million doses to 41 countries). The others are produced by private firms that have received vast amounts of public funding. Moderna, for instance, received $2.48 billion from the US government, while Pfizer received $548 million from the European Union and the German government. These firms put the public funding towards making a vaccine and then extracted enormous profits from their sales and further secured these profits through patents. This is one example of pandemic profiteering.

Information about the numbers of vaccines sold and transported to different parts of the world changes rapidly. Nonetheless, it is now acknowledged that many poorer nations will not have vaccines for their citizens before 2023, while the Global North has secured more vaccines than they require – enough to vaccinate their populations three times over. Canada, for instance, has enough vaccines to vaccinate its citizens five times. The Global North, with less than 14% of the world’s population, has secured more than half the total anticipated vaccines. This is known as vaccine hoarding or vaccine nationalism.

The governments of India and South Africa approached the World Trade Organisation (WTO) in October 2020 to ask for a temporary waiver of patent obligations under the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS). If the WTO had agreed to this waiver, these countries could have produced generic versions of the vaccine to distribute at low cost for a mass vaccination drive. However, the Global North led the opposition to this proposal, arguing that such a waiver – even in the midst of a pandemic – would stifle research and innovation (despite the fact that the vaccines were developed largely with public money). The Global North successfully blocked the application for the waiver in the WTO.

In April 2020, the World Health Organisation (WHO), with other partners, set up the COVID-19 Vaccines Global Access or COVAX. The point of COVAX is to ensure equitable access to the vaccines. The project is led by UNICEF; GAVI, The Vaccine Alliance; the Coalition for Epidemic Preparedness Innovations (CEPI); and the WHO. Despite the fact that the majority of the world’s countries signed on to the alliance, vaccines are not being distributed to the Global South in sufficient numbers. A study from December 2020 found that, during 2021, nearly seventy countries in the Global South will only be able to vaccinate one in ten people.

Rather than supporting the India-South Africa application for the waiver, COVAX backed a proposal for patent pooling called Covid-19 Technology Access Pool (C-Tap). This process would involve two or more patent holders agreeing to license their patents to one another or to any third party. COVAX has not received any contributions to date from pharmaceutical companies.

In May 2020, the WHO proposed to establish an international COVID-19 vaccine solidarity trial in which the WHO would coordinate trial sites in multiple countries. This would have led emerging vaccine candidates to enter clinical trials rapidly and transparently; they would have been tested in multiple populations and comparisons could have been made for specific strengths and limitations. Both Big Pharma and the countries of the North suffocated this proposal.

Joaquín Torres García (Uruguay), Energía Atómica (Atomic Energy), 1946.

Joaquín Torres García (Uruguay), Energía Atómica (Atomic Energy), 1946.

What would it take to produce basic vaccines for the world’s 7.7 billion people?

The production of vaccines varies based on the actual technological platform required for creating the particular infection mimicry to be used for the specific vaccine. For COVID-19 vaccines, there are many successful platforms. Two such instances have been the RNA vaccines (in the case of Moderna) and adenovirus vaccines (in the case of AstraZeneca). These technology platforms are robust, meaning that if the know-how (including trade secrets for the vaccine production) and skilled personnel are available and manufacturing lines are scaled-up and efficient, the vaccine could be produced for the people. The word ‘if’ is in italics because these are the most important impediments that stem from the capitalist logic of intellectual property rights and the long-term drive to undermine a public sector that centres the social good.

One intermediate approach to vaccine production attempts the large-scale manufacture of mimic proteins in fermentation tanks (the Novavax vaccine, for example, is manufactured in this way). For this platform, the absorption capacity and personnel with skills are more widespread. The quality control and assurance issues are more varied batch-to-batch in these platforms, which is a hurdle for widespread decentralised production.

There is a much simpler way to produce the vaccines: to grow the infectious agent, inactivate it (namely, to make it non-dangerous), and inject that into the body (such as Covaxin, the vaccine developed by Bharat in India). But there are problems here since it is not always easy to inactivate the harmful pathogen whilst still keeping it whole to develop the antibodies.

Alfred Eisenstaedt (USA), Student Nurses at Roosevelt Hospital (1938).

Alfred Eisenstaedt (USA), Student Nurses at Roosevelt Hospital (1938).

What would it take to administer vaccines for the 7.7 billion?

To widely administer the COVID-19 vaccines across the globe, we need to consider three elements:

  1. Public Health Systems. Effective vaccination programmes require robust public health systems. But these have been eroded by long-term austerity policies in many countries across the world. Therefore, there are insufficient numbers of skilled and practiced personnel to administer the vaccine; since these are sensitive vaccines, preparation and administration of the vaccine must be done by trained public health workers (both to ensure the vaccine is delivered optimally and to prevent side effects).
  2. Transportation and Cold Chains. Since regional and national vaccine production lines are not available, the vaccines need to be transported over long distances. Some COVID-19 vaccines that require an ultra-cold chain are simply impractical in much of the Global South.
  3. Medical Monitoring Systems. Finally, there need to be well-developed systems to monitor the impact of the vaccine. This requires long-term follow-up and both personnel and technologies that are often lacking in poorer nations, which have long been disadvantaged by the global economic order.
Otman Ghalmi (Democratic Way/Morocco), Dr. Nawal El-Saadawi (1931-2021), 2021.

Otman Ghalmi (Democratic Way/Morocco), Dr. Nawal El-Saadawi (1931-2021), 2021.

It is worthwhile to read and circulate the Alma-Ata Declaration (1978) on primary health care and the People’s Charter for Health (2000), both strong statements for a robust, humane approach to health care. The latter asks for a rejection of ‘patents on life’, which includes patents on vaccines. There is no alternative to a people’s vaccine, no alternative to life over profit.

The post The Vaccine Must Be a Common Good for Humanity first appeared on Dissident Voice.

Why are Effective and Inexpensive Chinese and Russian Vaccines Unavailable in Much of the West?

In 2016, I attended an information session about First Nations in Lax Kxeen (colonial designation Prince Rupert),1 “BC.” During a break, I conversed with some fellow attendees. They expressed skepticism to colonial provincial authorities being behind the intentional spreading of smallpox among First Nations people2 and that a vaccine was withheld from infected Indigenous individuals. The attendees insisted that there was no vaccine at that time for smallpox.

Yet, the English doctor Edward Jenner is celebrated for having discovered the smallpox vaccine in 1796. This is the predominant western account on the origin of the smallpox vaccination.

It is also recorded that inoculation against smallpox was already being practiced in Sichuan province by Taoist alchemists in the 10th century CE.3 The Chinese inoculators administered dead or attenuated smallpox collected from less virulent scabs, which were inserted into the nose on a plug of cotton. Inoculation may also have been practiced much earlier by the Chinese — some sources cite dates as early as 200 BCE.

China obviously has a historical background in strengthening the immune response of people. Yet, in the western media, one seldom reads or hears about the Chinese COVID-19 vaccines. Neither were we well informed about the effectiveness of the Russian COVID-19 vaccine — that was until recently, when some western nations have been coming up short on vaccine supplies. The Canadian government has been scrambling to meet the demand for vaccines since Pfizer shipments were held up. The focus of western state and corporate media seemed clearly on procuring supplies of the Pfizer (US), Moderna (US), and AstraZeneca (UK-Sweden) vaccines. This is despite effective, but less heralded, Russian and Chinese vaccines being available and at a more affordable price. South Korea’s Arirang News reported Russian test results that “its second COVID-19 vaccine is 100% effective.” CBC.ca found this success problematic; it depicted a political quandary in considering a Russian vaccine: “At first dismissed and ridiculed by Western countries, Russia’s Sputnik V vaccine has not only been rehabilitated; it’s emerging as a powerful tool of influence abroad for President Vladimir Putin.” France 24 concurred, hailing it as “a scientific and political victory for Vladimir Putin’s Russia.”

Would Canada refuse to consider securing vaccines from Russia to safeguard the health of Canadians to avoid granting Putin, derided by Canadian magazine Macleans as a “new Stalin,” a political victory? Why shouldn’t Russia be lauded for coming up first with a working and effective vaccine? What does it matter if the leader of that country receives recognition? Shouldn’t the national priority be obtaining the best vaccine to protect the health of citizens?

Medical data aside, western mass media has, apparently, been effective in stirring up a distrust of COVID-19 vaccines from China and Russia in comparison to western vaccines, as revealed in a YouGov poll of almost 19,000 people worldwide.

Hungary has been mildly criticized for going its own way in ordering the Russian vaccine. Hungary’s foreign minister, Péter Szijjártó, had no qualms and defended Budapest’s decision to buy two million doses of Russia’s Sputnik V vaccine.

The Czech Republic is also considering following Hungary in using Russian and Chinese vaccines that are still pending approval by the European Union.

Huge Potential Profits in Vaccines

Investigative journalist Matt Tabibi pointed out,

What Americans need to understand about the race to find vaccines and treatments for Covid-19 is that in the U.S., … the production of pharmaceutical drugs is still a nearly riskless, subsidy-laden scam.

The World Health Organization (WHO) director-general Tedros Adhanom Ghebreyesus strongly criticized big pharma for profiteering and vaccine inequalities. Adhanom charged that younger, healthier adults in wealthy countries were being prioritized for vaccination against COVID-19 before older people or health care workers in poorer countries and that markets were sought to maximize profitability.

In chapter VII of the e-book The 2020 Worldwide Corona Crisis: Destroying Civil Society, Engineered Economic Depression, Global Coup d’État and the “Great Reset” (December 2020, revised January 2021), professor Michel Chossudovsky writes:

The plan to develop the Covid-19 vaccine is profit driven.

The US government had already ordered 100 million doses back in July 2020 and the EU is to purchase 300 million doses. It’s Big Money for Big Pharma, generous payoffs to corrupt politicians, at the expense of tax payers.

The objective is ultimately to make money, by vaccinating the entire planet of 7.8 billion people for SARS-CoV-2….

The Covid vaccine is a multibillion dollar Big Pharma operation which will contribute to increasing the public debt of more than 150 national governments.

Imagine, if those thousands of people stay home, reduce contact with others, they may have survived the pandemic.4

Chossudovsky also questions the safety of the rushed testing and the need for a vaccine given that the WHO and the US Center for Disease Control and Prevention (CDC) both confirmed that Covid-19 is “similar to seasonal influenza.”5

Some Safety Concerns about Vaccines

A report raised alarm about at least 36 people who developed a rare, lethal blood disorder, called thrombocytopenia, after receiving either of the two approved COVID-19 vaccines in the US. A Miami obstetrician, Gregory Michael, just 56, died of a brain hemorrhage just 16 days after receiving a Pfizer vaccination. His thrombocytopenia had caused his platelets to drop to virtually zero.

A Johns Hopkins University expert on blood disorders, Jerry L. Spivak, who was uninvolved in Michael’s care, said that based on Michael’s wife’s description: “I think it is a medical certainty that the vaccine was related [to Michael’s death].”

In Israel, at least three people suffered Bell’s palsy, facial paralysis, after receiving the vaccine. Data from Pfizer and Moderna vaccine trials revealed seven COVID-19 participants had experienced Bell’s palsy in the weeks following vaccination.

In Norway, at least 23 people who received the Pfizer COVID-19 vaccine died. According to authorities, thirteen of the fatalities were associated to the vaccine’s side effects. In addition, 10 deaths shortly following vaccination were being probed in Germany.

Pfizer and Moderna use a novel vaccine based on mRNA. Following the deaths in Norway, Chinese health experts called for caution and the suspension of mRNA-based COVID-19 vaccines, especially for elderly people.

Regarding the safety of COVID-19 vaccines, the CDC reported the administration of over 41 million doses of COVID-19 vaccines in the US from 14 December 2020 through 7 February 2021. During this time, the Vaccine Adverse Event Reporting System received 1,170 reports of death (0.003%) among people vaccinated for COVID-19. Based on the extremely low figure, the CDC advised people that “COVID-19 vaccines are safe and effective” and “to get a COVID-19 vaccine as soon as you are eligible.”

Yet, it seems some Europeans distrust their own government-approved Covid-19 vaccines. A black market has arisen; two doses of unapproved Chinese vaccines have reportedly sold for as high as 7,000 yuan (£800) — almost 20 times the reported usual price.

Vaccine makers, Sinopharm and Sinovac, cautioned the public not to buy the vaccines online.

Chinese Vaccines and Profit-seeking

Chinese leader Xi Jinping has been magnanimous with what could be an extremely profitable property. Said Xi, “China is willing to strengthen cooperation with other countries in the research and development, production, and distribution of vaccines,”

“We will fulfill our commitments, offer help and support to other developing countries, and work hard to make vaccines a public good that citizens of all countries can use and can afford.”

Imagine that: making an in-demand product available as a “pubic good” instead of taking advantage of a seemingly dire situation to rake in huge profits. Africa, for one, is benefiting.

Back in October 2020, Fortune.com proclaimed in its headline: “World’s vaccine testing ground deems Chinese COVID candidate ‘the safest, most promising.’” The tests conducted in Brazil were large, human trials of the COVID-19 vaccines that included Johnson & Johnson, Pfizer, AstraZeneca, and China’s Sinovac and Sinopharm.

São Paulo Governor João Doria said,

The first results of the clinical study conducted in Brazil prove that among all the vaccines tested in the country, CoronaVac from Chinese developer Sinovacis the safest, the one with the best and most promising rates.

On 3 February 2021, the peer-review medical journal, The Lancet, published a study by Wu et al. who spoke to the urgent need for a vaccine against COVID-19 for the elderly. Their study found that the Chinese CoronaVac, containing inactivated SARS-CoV-2, is safe and well tolerated by the elderly.

Journalist Wei Ling Chua, who follows closely how events involving China are portrayed and perceived elsewhere, asked in an email on 12 February 2021:

1) till this date, there is no report of a single death or hospitalisation after taking China vaccine

2) unlike the capitalist west, China vaccine companies did not require nations to excuse them from legal liability from side effects.

Despite, western nations acknowledging many having died soon after taking the vaccine, they all claim that after investigation the cause of death not related to vaccine. But, why does death happen so soon after taking the vaccine?

Why following administration of a Chinese vaccine are there no reports of people dying soon afterwards?

Closing Comments

This essay does not explore the necessity for vaccination against COVID-19. Indeed, there are grounds to be skeptical of the necessity for all people to be vaccinated. However, if COVID-19 is genuinely an urgent health issue,6 then why would governments play politics with the health of their populace?

  1. The city’s name is an eponym for Prince Rupert of the Rhine, a European elitist who never set foot on the Pacific coast. For the Ts’msyen: “Place names are usually rooted in the natural world and the land they refer to.” See Kenneth Campbell, Persistence and Change: A History of the Ts’msyen Nation (Prince Rupert, [sic] BC: First Nation Educational Council, 2005): 10. Author Kenneth Campbell commented, “By writing and saying the name name in [Sm’algyax, the Ts’msyen language], both the language and the people are honored.” (p. 10)
  2. Tom Swanky, The Great Darkening: The True Story of Canada’s “War” of Extermination on the Pacific plus The Tsilhqot’in and other First Nations Resistance (Burnaby, BC: Dragon Heart Enterprises, 2012). See also an interview with Tom Swanky.
  3. Robert Temple, The Genius of China: 3,000 Years of Science, Discovery and Invention (London: Prion Books, 2002): 135-137.
  4. Click on the following link to access the complete E-book consisting of a Preface, Highlights and Nine Chapters.
  5. For more on “the absolute and relative ‘flu-like’ risk of death from a SARS-CoV-2 infection” see “Review of calculated SARS-CoV-2 infection fatality rates: Good CDC science versus dubious CDC science, the actual risk that does not justify the ‘cure’ – By Prof Joseph Audie,” ResearchGate.
  6. Even about this be skeptical; research and inform yourself; and draw your own conclusions.
The post Why are Effective and Inexpensive Chinese and Russian Vaccines Unavailable in Much of the West? first appeared on Dissident Voice.

Rushing a Vaccine to Market for a Vanishing Virus

More than 100 companies are competing to be first in the race to get a COVID-19 vaccine to market. It’s a race against time, not because the death rate is climbing but because it is falling – to the point where there will soon be too few subjects to prove the effectiveness of the drug.

Pascal Soriot is chief executive of AstraZeneca, a British-Swedish pharmaceutical company that is challenging biotech company Moderna, the U.S. frontrunner in the race. Soriot said on May 24th, “The vaccine has to work and that’s one question, and the other question is, even if it works, we have to be able to demonstrate it. We have to run as fast as possible before the disease disappears so we can demonstrate that the vaccine is effective.”

COVID-19, like other coronaviruses, is expected to mutate at least every season, raising serious questions about claims that any vaccine will work. A successful vaccine has never been developed for any of the many strains of coronaviruses, due to the nature of the virus itself; and vaccinated people can have a higher chance of serious illness and death when later exposed to another strain of the virus, a phenomenon known as “virus interference.” An earlier SARS vaccine never made it to market because the laboratory animals it was tested on contracted more serious symptoms on re-infection, and most of them died.

Researchers working with the AstraZeneca vaccine claimed success in preliminary studies because its lab monkeys all survived and formed antibodies to the virus, but data reported later showed that the animals all became infected when challenged, raising serious questions about the vaccine’s effectiveness.

Moderna has gotten fast-track approval from the FDA and managed to skip animal trials altogether before rushing to human trials. Its candidate is a “messenger RNA” vaccine, a computer-generated replica of an RNA component that carries genetic information controlling the synthesis of proteins. No mRNA vaccine has ever been approved for marketing or proven in a large-scale clinical trial. As explained in Science magazine, RNA that invades from outside the cell is the hallmark of a virus, and our immune systems have evolved ways to recognize and destroy it. To avoid that, Moderna’s mRNA vaccine sneaks into cells encapsulated in nanoparticles, which aren’t easily degraded and can cause toxic buildup in the liver.

These concerns, however, have not deterred the U.S. Department of Health and Human Services (HHS), which is proceeding at “Warp Speed” to get the new technologies tested on the American population before the virus disappears through mutation and natural herd immunity. HHS has already agreed to provide up to $1.2 billion to AstraZeneca and $483 million to Moderna to develop their experimental candidates. “As American taxpayers, we are justified in asking why,” writes William Haseltine in Forbes. Both companies have attracted billions from private investors and don’t need taxpayer money, and the government’s speculative bets are being made on unproven technologies in the early stages of testing.

The argument at one time was that the magnitude of the crisis justified the risk, but the virus is now disappearing of its own accord. The computer-modeled projection of 2.2 million U.S. deaths issued by Imperial College London (a business partner of AstraZeneca), triggering shutdowns across the United States, was subsequently found to be “wildly” overblown. The model was described in the UK Telegraph on May 16 as “the most devastating software mistake of all time.” The researchers wrote that “we would fire anyone for developing code like this” and that the question was “why our Government did not get a second opinion before swallowing Imperial’s prescription.”

The U.S. Centers for Disease Control has also revised its projections. Experts disagree on what the new data means, but according to an expert at the Montreal Economic Institute, “The most likely CDC scenario now estimates that the coronavirus mortality rate for infected people is between 0.2% and 0.3%. This is a far cry from the 3.4% figure that had been put forward by the WHO at the start of the pandemic.”

In other news from the CDC, on May 23 the agency reported that the antibody tests used to determine whether people have developed an immunity to the virus are too unreliable to be used.

But none of this seems to be dimming the hype and the deluge of investment money being thrown at the latest experimental vaccines. And perhaps that is the point of the exercise – to extract as much money as possible from gullible investors, including the US government, before the public discovers that the fundamentals of these stocks do not support the media hype.

Moderna: A Multibillion-Dollar “Unicorn” That Has Never Brought a Product to Market

Moderna in particular has been suspected of pumping its stock price with unreliable preliminary test data. On May 18, Moderna’s stock jumped by as much as 30%, after it issued a press release announcing positive results from a small preliminary trial of its coronavirus vaccine. After the market closed, the company announced a stock offering aimed at raising $1 billion; and on May 18 and 19, Moderna executives dumped nearly $30 million worth of stock for a profit of $25 million.

On May 19, however, the stock rocketed back down, after STAT News questioned the company’s test results. An antibody response was reported for only eight of the 45 patients, not enough for statistical analysis. Was the response significant enough to create immunity? And what about the other 37 patients?

Robert F. Kennedy Jr. called the results a “catastrophe” for the company. He wrote on May 20:

Three of the 15 human guinea pigs in the high dose cohort (250 mcg) suffered a “serious adverse event” within 43 days of receiving Moderna’s jab. Moderna … acknowledged that three volunteers developed Grade 3 systemic events, defined by the FDA as “Preventing daily activity and requiring medical intervention.”

Moderna allowed only exceptionally healthy volunteers to participate in the study. A vaccine with those reaction rates could cause grave injuries in 1.5 billion humans if administered to “every person on earth”.

A volunteer named Ian Haydon buoyed the markets when he appeared on CNBC to say he felt fine after getting the vaccine. But he later revealed that after the second jab, he got chills and a fever of over 103°F (39.4°C), lost consciousness, and “felt more sick than he ever has before.”

Those were just the short-term adverse effects. Long-term systemic effects including cancer, Alzheimer’s disease, autoimmune disease, and infertility can take decades to develop. But the stage is already being set for mandatory vaccinations that will be “deployed” by the U.S. military as soon as the end of the year. The HHS in conjunction with the Department of Defense has awarded a $138 million contract for 600 million syringes prefilled with coronavirus vaccine, individually marked with trackable RFID chips. That’s enough for two doses for nearly the entire U.S. population. One hundred million are to be supplied by year’s end.

Fortunately for vaccine manufacturers and investors, they do not have to worry about the drugs’ side effects, since the National Vaccine Injury Compensation Program and the 2005 PREP Act protect them from liability for vaccine injuries. Damages are imposed instead on the US government and US taxpayers.

What Moderna could have to worry about, however, is criminal action by the Securities Exchange Commission. By May 22, Moderna’s stock was down by 26% from its earlier high, making its 30% rise on a misleading press release look like a “pump and dump” scheme. On CNBC on May 19, former SEC lawyer Jacob Frankel said its stock offering on the heels of hyped news was the type of action that would draw scrutiny by the SEC, and that it could have a criminal component.

Why All the Hype? Moderna’s mRNA Vaccine

It wasn’t the first time Moderna’s stock had skyrocketed on a well-timed press release. On February 24, the World Health Organization said to prepare for a global pandemic, collapsing stock markets around the world. Most stocks collapsed, but Moderna’s shot up by nearly 30%, after it reported on February 25 that testing on humans would begin in March. Mega-investors made tens of millions of dollars in a single day, including BlackRock, the world’s largest asset manager, which made $68 million just on February 25. BlackRock was called “the fourth branch of government” after it was tasked in March with dispensing up to $4.5 trillion in Federal Reserve credit through “special purpose vehicles” established by the Treasury and the Fed.

Moderna has other friends in high places, including the Pentagon. Several years ago, Moderna received millions of dollars from the Pentagon’s Defense Advanced Research Projects Agency (DARPA), as well as from the Bill and Melinda Gates Foundation. Moderna’s stock has more than tripled this year, taking it to a market cap of over $22 billion. STAT News called it “an astonishing feat for a company that currently sells zero products.” Many of the companies actively developing COVID-19 vaccines have longer and more impressive track records. Why all the investor interest in this “unicorn” startup that went public only in 2018 and has no record of market success?

The major advantage of mRNA vaccines is the speed with which they can be deployed. Created in a lab rather than from a real virus, they can be mass-produced cost-effectively on a large scale and do not require uninterrupted cold storage. But this speed comes at the risk of major side effects. In a 2017 TED talk called “Rewriting the Genetic Code,” Moderna’s current chief medical officer Dr. Tal Zaks said, “We’re actually hacking the software of life ….”

As explained by a medical doctor writing in the UK Independent on May 20:

Moderna’s messenger RNA vaccine … uses a sequence of genetic RNA material produced in a lab that, when injected into your body, must invade your cells and hijack your cells’ protein-making machinery called ribosomes to produce the viral components that subsequently train your immune system to fight the virus. …

In many ways, the vaccine almost behaves like an RNA virus itself except that it hijacks your cells to produce the parts of the virus, like the spike protein, rather than the whole virus. Some messenger RNA vaccines are even self-amplifying…. There are unique and unknown risks to messenger RNA vaccines, including the possibility that they generate strong type I interferon responses that could lead to inflammation and autoimmune conditions.

A lab-created self-amplifying virus encapsulated in nanoparticles that evade the cell’s defenses by stealth sounds a lot like the “stealth viruses” that are classified as “bioweapons,” and that could explain DARPA’s interest in the technology. In a 2010 document titled “Biotechnology: Genetically Engineered Pathogens,” the US Air Force acknowledged that it was studying “genetically engineered pathogens that could pose serious threats to society,” including “binary biological weapons, designer genes, gene therapy as a weapon, stealth viruses, host-swapping diseases, and designer diseases.” DARPA was behind the creation of both DNA and RNA vaccines, funding their early research and development by Moderna as well as by Inovio Pharmaceuticals Inc.

In December 2017, over 1,200 emails released under open records requests revealed that the U.S. military is now the top funder behind the controversial “genetic extinction” technology known as “gene drives.” As investigative reporter Whitney Webb observed in a May 4 article, “these genetic ‘kill switches’ could also be inserted into actual humans through artificial chromosomes, which – just as they have the potential to extend life – also have the potential to cut it short.” Biowarfare is forbidden under international treaty, but the army’s Medical Research Institute of Infectious Diseases at Fort Detrick says its investigations are to “protect the warfighter from biological threats” and to protect civilians from threats to public health. Even assuming that is true, are the army’s technicians proficient enough to tinker with the human genetic code without hitting a kill switch or two by mistake?

The military is thinking about war, the pharmaceutical companies and investors are thinking about profits, the politicians are thinking about getting the country back to work, and even the regulators are bypassing proper safety tests in the rush to get the entire global population vaccinated before the virus disappears. It is left to us, the recipients of these novel untested GMO vaccines, to demand some serious vetting before the military shows up at our doors with their prefilled RFID-chipped syringes some time later this year.