mRNA “Vaccines”, Eugenics and the Push for Transhumanism
Posted: Thu Sep 02, 2021 5:32 am
mRNA “Vaccines”, Eugenics and the Push for Transhumanism
https://www.newbraveworld.org/mrna-vacc ... d-the-push
The worldwide rollout of mRNA “vaccines” is part of a much larger agenda that encompasses eugenics and transhumanism. This agenda is being funded and promoted by a network of global institutions, politicians, and billionaire technocrats.
Researchers from the Salk Institute 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 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 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.
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. 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 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 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”.
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” . 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 org that provides “reproductive health care” .From 2019-2020 the org committed over 350k abortions and has been criticized as “steering resources away from women’s health and toward abortion.” Planned Parenthood has its roots in Eugenics ideals.
Planned Parenthood was founded by Margaret Sanger, who, far from a “birth control activist”, as the mainstreamwould have you believe, was a racist eugenicist who sought to rid the world of “unfit” human stock. 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. 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 notion that the disease is caused by a virus is likely false.
Paralytic polio appeared suddenly in the US in the early 1900s with continual, dramatic fluctuations in cases – 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.
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 Scobey and Goddard 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, were illustrated by Rachel Carson. Silent Spring.
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 conclusion 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.
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 Int’l Planned Parenthood Foundation. May’s views on immigration were radical, 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 org 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 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.
Those with keen perception may be alarmed when reading excerpts 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, “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.
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, 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, most of which have not been fully FDA approved, only authorized under emergency use (EUA), and labeled as “investigational” products, a fact that many people are unaware of. 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. And on the 23rd of August, the FDA granted the approval. But with millions of vaccines already administered under EUA, what was 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 constitutes one of the fastest ever. Although the phase three clinical trials for Pfizer, Moderna, and Janssen are all two years in duration, the FDA was careful to never clearly state their position with regards to minimum follow-up prior to consideration for approval.
Longer, placebo-controlled trials are paramount to assessing vaccine safety. Vaccine manufacturers, 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, the
have no way to accurately measure long-term safety. The same goes for Pfizer.
In an article for the British Medical Journal, Peter Doshi quotes the FDA, 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. Indeed, of the 200+ drugs approved by the FDA between 2000 and 2010, one-third of them were found to have serious safety concerns.
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.
Wow such deception was put upon us.
https://www.newbraveworld.org/mrna-vacc ... d-the-push
The worldwide rollout of mRNA “vaccines” is part of a much larger agenda that encompasses eugenics and transhumanism. This agenda is being funded and promoted by a network of global institutions, politicians, and billionaire technocrats.
Researchers from the Salk Institute 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 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 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.
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. 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 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 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”.
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” . 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 org that provides “reproductive health care” .From 2019-2020 the org committed over 350k abortions and has been criticized as “steering resources away from women’s health and toward abortion.” Planned Parenthood has its roots in Eugenics ideals.
Planned Parenthood was founded by Margaret Sanger, who, far from a “birth control activist”, as the mainstreamwould have you believe, was a racist eugenicist who sought to rid the world of “unfit” human stock. 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. 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 notion that the disease is caused by a virus is likely false.
Paralytic polio appeared suddenly in the US in the early 1900s with continual, dramatic fluctuations in cases – 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.
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 Scobey and Goddard 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, were illustrated by Rachel Carson. Silent Spring.
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 conclusion 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.
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 Int’l Planned Parenthood Foundation. May’s views on immigration were radical, 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 org 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 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.
Those with keen perception may be alarmed when reading excerpts 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, “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.
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, 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, most of which have not been fully FDA approved, only authorized under emergency use (EUA), and labeled as “investigational” products, a fact that many people are unaware of. 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. And on the 23rd of August, the FDA granted the approval. But with millions of vaccines already administered under EUA, what was 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 constitutes one of the fastest ever. Although the phase three clinical trials for Pfizer, Moderna, and Janssen are all two years in duration, the FDA was careful to never clearly state their position with regards to minimum follow-up prior to consideration for approval.
Longer, placebo-controlled trials are paramount to assessing vaccine safety. Vaccine manufacturers, 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, the
have no way to accurately measure long-term safety. The same goes for Pfizer.
In an article for the British Medical Journal, Peter Doshi quotes the FDA, 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. Indeed, of the 200+ drugs approved by the FDA between 2000 and 2010, one-third of them were found to have serious safety concerns.
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.
Wow such deception was put upon us.