RYAN MATTERS: “mRNA ‘Vaccines’, Eugenics & the Push for Transhumanism”

“You have to be born lucky in the sense that you have to have the right genes. You have to have a certain gene. I have a certain gene. And I really was — you know, I had a — a good gene pool from the standpoint of that. I have Ivy League education, smart guy, good genes. I have great genes and all that stuff, which I’m a believer in. I’m a gene believer. You have to have the right — the right genes.”

~Donald Trump


August 29, 2021

by Ryan Matters, OffGuardian

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method can be used to directly introduce RNA into whole tissues and embryos (R.W.M., C. Holt, and I.M.V., unpublished results), raising the possibility that liposome-mediated mRNA transfection might offer yet another option in the growing technology of eukaryotic gene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.”

Eugenics ‘Ideals’ Inspired the Nazis

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, causation doesn’t equal correlation, 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.

Diseases 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 experts “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:

Although 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”

“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 the 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 that U.S. President Trump endorsed and funded millions to). 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 noncommunicable 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 soulless, pharmaceutical sock puppets like Dr Anthony Fauci, the director of the U.S. National Institute of Allergy and Infectious Diseases whose been spewing lies 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), Kary 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 smart phone, 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 roll out 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 roll out 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.


~via Off-Guardian.org


JON RAPPOPORT on “The Human Heart, Not Vaccines.”

Imagine a child brought into this world who has two loving parents close to him. The mother breastfeeds him. The child is free to play. He has friends. He eats fresh simple food. The immediate world around him contains no every-day ominous human threats.

In this setting, his health and vitality expand.

The idea of vaccines—even if they did safely prevent disease (they don’t)—would be absurd.

Vaccination would be an interruption of life.

It would force the child’s body to deal with an unnatural and unnecessary intrusion.

Any sane person looking at the ALIVENESS of the child, day after day, would immediately understand the insanity of a vaccine.

Likewise, the notion that a child who is born into a threatening, cold, and unhealthy world could benefit from a vaccine is also insane. What needs to be changed is the immediate world the child is born into.

The quick fix of a vaccine is no fix at all.

In the same way, if a person who is exposed to toxic chemicals in the environment therefore develops cancer, no amount of prior fiddling with his genes would have prevented the cancer. The environment needs to be changed.

To say that modern medicine has made an overreach would be a vast understatement. Every negative blip the environment imposes on a child is viewed as a symptom of a disease which must be treated.

Another interruption in the flow of life.

And the first test of that health, for a baby, is the warm love of two parents. Is it there or isn’t it?

If it isn’t, the baby immediately has to make unhealthy adjustments.

Now we come to another form of vaccination, so to speak. The modern education system. Its basic purpose seems to be the prevention of unique individual vitality.

Vitality, of course, is viewed as a disease.

VITALITY.

And when scientists decided they had to find the tiny organisms causing these negative blips, they eventually focused on a concept called VIRUS. They invented a closed system for discovering these viruses—a self-fulfilling prophecy. A claim of virus-isolation that was no isolation at all; a claim of sequencing the genome of the virus which was nothing more than a simulation of possible cobbled-together genetic information. In other words, nonsense.

The basic human immune system is HEALTH. VITAL LIFE FORCE.

It isn’t a germ-killing military machine inside the body.

HEALTH overrides illness.

SPIRIT. VITALITY. HEALTH. POWER. THE UNIQUE INDIVIDUAL.


~via No More Fake News


MEGAN REDSHAW: “COVID Vaccine Death Numbers Are Skyrocketing”

by Megan Redshaw

VAERS data released today by the CDC showed a total of 438,441 reports of adverse events from all age groups following COVID vaccines, including 9,048 deaths and 41,015 serious injuries between Dec. 14, 2020 and July 2, 2021.

Data released today by the Centers for Disease Control and Prevention (CDC) included 9,049 reports of deaths, across all age groups, following COVID vaccines — an increase of more than 2,000 compared with the previous week. The data comes directly from reports submitted to the Vaccine Adverse Event Reporting System (VAERS).

VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.

Every Friday, VAERS makes public all vaccine injury reports received as of a specified date, usually about a week prior to the release date.

Data released today show that between Dec. 14, 2020 and July 2, 2021, a total of 438,441 total adverse events were reported to VAERS, including 9,048 deaths — an increase of 2,063 over the previous week. There were 41,015 serious injury reported during the same time period — up 6,950 compared with last week.

In the U.S, 328.9 million COVID vaccine doses had been administered as of July 2. This includes: 134 million doses of Moderna’s vaccine, 182 million doses of Pfizer and 13 million doses of the Johnson & Johnson (J&J) COVID vaccine.

Of the 9,048 deaths reported as of July 2, 22% occurred within 48 hours of vaccination, 15% occurred within 24 hours and 37% occurred in people who became ill within 48 hours of being vaccinated.

This week’s data for 12- to 17-year-olds show:

13,385 total adverse events, including 801 rated as serious and 14 reported deaths among 12- to 17-year-olds. Two of the nine deaths were suicides.

• The most recent reported death includes a 13-year-old boy (VAERS I.D. 1431289) with a previous history of COVID who suffered cardiac arrest and died 17 days after vaccination with Pfizer.Other reports include a 13-year-old boy (VAERS I.D. 1406840) who died two days after receiving a Pfizer vaccine, three 15-year-olds (VAERS I.D. 1187918, 1382906 and 1242573), four 16-year-olds (VAERS I.D. 1420630, 1426828, 1225942 and 1386841) and three 17-year-olds (VAERS I.D. 1199455, 1388042 and 1420762).

1,934 reports of anaphylaxis among 12- to 17-year-olds with 99% of cases

• attributed to Pfizer’s vaccine, 1.1% to Moderna and 0.2% (or four cases) to J&J.

347 reports of myocarditis and pericarditis (heart inflammation) with 343 attributed to Pfizer’s vaccine.

57 reports of blood clotting disorders, 56 attributed to Pfizer and 1 attributed to Moderna.

This week’s total VAERS data, from Dec. 14, 2020 to July 2, 2021, for all age groups show:

• 22% of deaths were related to cardiac disorders.

• 50% of those who died were male, 45% were female and the remaining death reports did not include gender of the deceased.

• The average age of death was 74.7.

• As of July 2, 2,678 pregnant women reported adverse events related to COVID vaccines, including 994 reports of miscarriage or premature birth.

• Of the 4,456 cases of Bell’s Palsy reported, 59% were attributed to Pfizer vaccinations, 39% to Moderna vaccine and 7% to J&J.

• 398 reports of Guillain-Barré Syndrome, with 47% of cases attributed to Pfizer, 40% to Moderna and 19% to J&J.

121,092 reports of anaphylaxis with 46% of cases attributed to Pfizer’s vaccine, 46% to Moderna and 7% to J&J.

8,256 reports of blood clotting disorders. Of those, 3,959 reports were attributed to Pfizer, 2,699 reports to Moderna and 1,552 reports to J&J.

1,796 cases of myocarditis and pericarditis with 1,177 cases attributed to Pfizer, 563 cases to Moderna and 52 cases to J&J’s COVID vaccine.

Pfizer says boosters needed, U.S. federal health agencies, scientists disagree

As The Defender reported today, U.S. federal health agencies and the maker of one of the most popular COVID vaccines are publicly at odds over if or when fully vaccinated people will need a third “booster” dose.

Pfizer announced Thursday it will seek Emergency Use Authorization from the FDA in August for a third dose of its COVID vaccine. The drugmaker predicted those who have been fully vaccinated will need a booster shot within six to 12 months of receiving their second dose of the Pfizer vaccine.

But the U.S.Department of Health and Human Services (HHS) hours later issued a joint statementby the FDA and Centers for Disease and Control and Prevention (CDC) saying, “Americans who have been fully vaccinated do not need a booster shot at this time.”

The HHS statement did not explicitly mention Pfizer, but said “a science-based, rigorous process” headed by the CDC, FDA and the National Institutes of Health would determine when or whether boosters were necessary.

Pfizer’s assertions about the need for boosters contradict other research, and several experts pushed back against the claim.

“There’s really no indication for a third booster or a third dose of an mRNA vaccine, given the variants that we have circulating at this time,” Dr. Céline Gounder, an infectious disease specialist at Bellevue Hospital Center in New York, told the New York Times. “In fact, many of us question whether you will ever need boosters.”

John P. Moore, professor of microbiology and immunology at Weill Cornell Medicine, told the Washington Post:

“No one is saying we’ll never need a booster, but to say we need it now and give the public the impression the vaccines are failing and something needs to be done as a matter of urgency. … The time isn’t now. The decisions that are going to be made will be made by federal agencies.”

Pfizer and BioNTech are developing a version of their COVID vaccine that targets the Delta variant, The New York Times reported this week. The companies expect to begin clinical trials of the vaccine in August.

Pfizer and BioNTech reported — based on their own studies that have not been published, nor peer-reviewed, according to the Times — that a booster given six months after the second dose of vaccine increased the potency of antibodies against the original virus and the Beta variant by five- to tenfold.

Vaccine efficacy may decline six months after immunization, the companies said in a news release, and booster doses may be needed to fend off virus variants. The vaccine makers said they will submit their findings to the FDA in the coming weeks, a step toward gaining authorization for booster shots.

17-year-old student required to get vaccinated suffers heart condition

Concerns around COVID vaccines and heart inflammation, especially in young males, continue to circulate. But according to an update posted today on the CDC website, the agency’s researchers have concluded the benefits of the vaccine outweigh the risks of myocarditis after vaccination.

European drug regulators today announced they also have found a “possible link” between a “very rare heart inflammation” and the Pfizer and Moderna vaccines, but sided with U.S. regulators, saying they also believe the benefits of the shots outweighed any risks.

Meanwhile, The Defender continues to report on teens who have experienced heart issues after taking the vaccines — including a 17-year-old student who developed symptoms of a heart condition about one week after his first dose of Pfizer’s COVID and subsequently was diagnosed with a heart condition.

The teen’s father, Fabio Berlingieri, told “Fox & Friends” his son had COVID and recovered, but was required to get the vaccine in order to play soccer.

Fox News medical contributor Dr. Nicole Saphier, who appeared in the interview with Berlingieri, said the way the New York Times and the CDC are presenting the data regarding the adverse effects of vaccines in adolescents is “irresponsible.”

“They cherry-pick the way they present the data. It’s an all or none approach. They say either adolescents are fully vaccinated or every single one of them is going to get COVID-19. That’s the way they are balancing it right now,” Saphier said.

Saphier said more weight should be given to potential adverse effects, like myocarditis and other heart inflammation issues, when deciding who should be vaccinated. She also encouraged the FDA to look closer at vaccines before recommending a universal policy.

Hundreds injured by COVID vaccines turn to GoFundMe for help

As reports of adverse events to COVID vaccines continue to grow in number, those injured by the vaccines are struggling to pay their medical bills.

As The Defender reported July 8, more than 180 people injured by COVID vaccines have had to turn to GoFundMe for help with large medical bills and other expenses, including Emma Burkey — the high school senior who underwent three brain surgeries due to blood clots after receiving J&J’s COVID vaccine.

People facing huge medical bills after being injured by COVID vaccines have few options, beyond what their own health insurance covers. That’s because under federal law, vaccine makers are shielded from liability.

Those injured by COVID vaccines can only file a claim for compensation through the Countermeasures Injury Compensation Program (CICP), run by HHS.

Since June 1, the CICP reported 869 pending cases but offered no further information. Since the program’s inception in 2010, only 29 claims have been paid, with an average payout of around $200,000. The other 452 claims (91.4%) were denied. Ten claims won approval but were deemed ineligible for compensation.

Biden plans to deploy federal teams in door-to-door COVID vaccine campaign

Making no mention of any safety concerns related to the vaccines, President Joe Biden this week announced plans to ramp up the federal government’s efforts to get more Americans vaccinated under a new “door-to-door” program.

As The Defender reported this week, under Biden’s program, the White House will deploy teams of officials from the CDC, Federal Emergency Management Administration and other federal health agencies. Biden suggested the unique door-knocking approach was needed now that “we are continuing to wind down the mass vaccination sites that did so much in the spring.”

Biden said the administration will also “step up efforts to get vaccines to doctors who serve younger people so that adolescents ages 12 to 18 can get vaccinated and — as they go for back-to-school check-ups or getting ready for their physicals they need for fall sports.”

Biden cited concerns over the COVID Delta variant, which he said is more transmissible and has forced some European countries to return to lockdowns. He did not mention any of the safety concerns previously noted by the CDC and FDA, including blood clots and heart inflammation, associated with the vaccines.

Number of cases among fully vaccinated continue to climb

Reports of COVID breakthrough cases among fully vaccinated people continue to rise, as The Defender reported earlier this week. As of June 28, the CDC reported 4,686 breakthrough cases resulting in death and hospitalization.

Nearly 30 people in Louisiana who were fully vaccinated against COVID died from the virus, according to the Louisiana Department of Health (LDH). Dr. Joseph Kanter, LDH state health officer and medical director, said 27 people between the ages of 28 and 93 have died with COVID more than two weeks after being fully vaccinated.

According to the San Francisco Examiner, more than 7,550 breakthrough cases have been reported, through June 23, in Californians who were fully vaccinated. Most cases were minor, but 62 people died from COVID, according to the California Department of Public Health.

California’s public health agency reported 584 fully vaccinated people had been hospitalized with COVID infection, but hospitalization status wasn’t available for 46% of post-vaccination cases. On July 7, state health officials reported 2,013 new infections among all Californians, including 24 deaths.

According to a report by the Tennessee Department of Health (TDH), breakthrough cases have resulted in 140 hospitalizations and 20 deaths in the state. As of May 1, TDH has not counted all breakthrough cases as the CDC “asked that only severe outcomes (hospitalization or death) be reported.”

123 days and counting, CDC ignores The Defender’s inquiries

According to the CDC website, “the CDC follows up on any report of death to request additional information and learn more about what occurred and to determine whether the death was a result of the vaccine or unrelated.”

On March 8, The Defender contacted the CDC with a written list of questions about reported deaths and injuries related to COVID vaccines. After repeated attempts, by phone and email, to obtain a response to our questions, a health communications specialist from the CDC’s Vaccine Task Force contacted us on March 29 — three weeks after our initial inquiry.

The individual received our request for information from VAERS, but said she had never received our list of questions, even though employees we talked to several times said CDC press officers were working through the questions and confirmed the representative had received them. We provided the list of questions again along with a new deadline, but never received a response.

On May 19, a CDC employee said our questions had been reviewed and our inquiry was pending in their system, but would not provide us with a copy of the response. We were told we would be contacted by phone or email with the response.

We have contacted the CDC numerous times since and were told nobody knew the specialist from the agency’s Vaccine Task Force who contacted us in March, and our request was still pending in the system. It has been 123 days since we sent our first email inquiring into VAERS data and reports and we have yet to receive a response.

Children’s Health Defense asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.

~via HumansAreFree.com

DONALD TRUMP: “Everybody, Go Get Your Shot.”

“The FDA said it, everybody said it. Any article you read said it couldn’t be done. It would be years and years, I handed the new administration what everyone is now calling a modern day medical miracle. And that means that 100% of the increased availability that we have now was initiated by our administration. 100%. In fact, the director of National Institutes of Health, Francis Collins, he’s Fauci’s boss, actually, I think he’s a Democrat too, by the way, recently said that our Operation Warp Speed was absolutely breathtaking and that the Trump administration deserves full credit, which we do. What has taken place over the last year under our administration would have taken any other precedent at least five years. And we got it done in nine months. Everyone says five years, oh, five years. By the time I left that magnificent house at 1600 Pennsylvania Avenue, almost 20 million Americans had already been vaccinated. 1.5 million doses were administered on my final day alone. 1.5 million in a day. Never let them forget. This was us. We did this. And the distribution is moving along, according to our plan. And it’s moving along really well. We had the military, what they’ve done, our generals and all of the people, what they’ve done is incredible. So everybody, go get your shot.”

~Donald Trump, 2/28/2021 CPAC speech

 

“The FDA said it, everybody said it. Any article you read said it couldn’t be done. It would be years and years, I handed the new administration what everyone is now calling a modern day medical miracle. Some say, it’s the greatest thing to happen in hundreds of years, two vaccines produced in record time with numerous others on the way, including the Johnson and Johnson vaccine that was approved just yesterday.

“And therapeutic relief also, if you’re sick, we have things now that are incredible. What has taken place over the last year under our administration would have taken any other precedent at least five years. And we got it done in nine months. Everyone says five years, oh, five years.

“Can you imagine if you had to go through what all of the countries of the world who are now getting the vaccine or soon will be getting it from various companies, but can you imagine if all of those countries had to go through what they’ve been going through over the last year? You’d lose hundreds of millions of people. I pushed the FDA like they have never been pushed before. They told me that loud and clear. They have never been pushed like I pushed them. I didn’t like them at all, but once we got it done, I said, I now love you very much. What the Trump administration has done with vaccines has in many respects, perhaps saved large portions of the world. Not only our country, but large portions of the world.

“Not only did we push the FDA far beyond what the bureaucrats wanted to do. We also put up billions and billions of dollars, 10 billion to produce the vaccines before we knew they were going to work. It was called a calculated bet or a calculated risk. We took a risk because if we didn’t do that, you still wouldn’t have the vaccines. You wouldn’t have them for a long time. So think of that, we took this bet. We made a bet because we thought we were on a certain track, but you’d be starting to make them right now. It’d be a long time before you ever saw. It takes 60 to 100 days to manufacture and inspect new doses. And that means that 100% of the increased availability that we have now was initiated by our administration. 100%. In fact, the director of National Institutes of Health, Francis Collins, he’s Fauci’s boss, actually, I think he’s a Democrat too, by the way, recently said that our Operation Warp Speed was absolutely breathtaking and that the Trump administration deserves full credit, which we do. And as conservatives and Republicans, never forget that we did it. Never let them take the credit because they don’t deserve the credit. They just followed now, they’re following our plan, but this has been something that they really call, they call it an absolute miracle. Joe Biden is only implementing the plan that we put in place. And if we had an honest media, which we don’t, they would say it loud and clear. By the time I left that magnificent house at 1600 Pennsylvania Avenue, almost 20 million Americans had already been vaccinated. 1.5 million doses were administered on my final day alone. 1.5 million in a day. Yet Biden said just a few days ago that when he got here, meaning The White House, there was no vaccine. He said, there’s no vaccine. Oh, good. Say it again, Joe. Now I don’t think he said that, frankly, in a malicious way. I really don’t. I actually believe he said that because he didn’t really know what the hell was happening.

“Never let them forget. This was us. We did this. And the distribution is moving along, according to our plan. And it’s moving along really well. We had the military, what they’ve done, our generals and all of the people, what they’ve done is incredible. But remember, we took care of a lot of people, including, I guess on December 21st, we took care of Joe Biden. Cause he got his shot. He got his vaccine. He forgot. It shows you how un-painful all that vaccine shot is. He forgot so it wasn’t very traumatic obviously, but he got his shot and it’s good that he got his shot. So everybody, go get your shot.”

 

 

~via Rev.com

JAMES CORBETT: “Exploring the Oxford-AstraZeneca Eugenics Links” — with Whitney Webb

SHOW NOTES AND MP3: https://www.corbettreport.com/?p=40180​

Even some in the independent media have bought into the hype surrounding the Oxford-AstraZeneca COVID vaccine and its “non-profit” nature. But once you peel back the layers of obfuscation you quickly find not only the profit motive hiding underneath, but the dark specter of eugenics. Whitney Webb of Unlimited Hangout joins us to discuss her recent article, “Developers of Oxford-AstraZeneca Vaccine Tied to UK Eugenics Movement.”

 

 

~via Corbett Report Extras