“Casey Means was a Stanford-educated surgeon. Her brother Calley was a lobbyist for pharma and the food industry. Both quit their jobs in horror when they realized how many people were being killed by the systems they participated in. This is an amazing story.”
“The new campaign targets young adults directly through a series of ads featuring “diverse, sexy images” and edgy music, accompanying the message that it doesn’t matter who you are, you are at risk because “HPV Fucks Everybody.”
“There are currently 80 cases pending in federal court against Merck alleging Gardasil caused injuries and the federal Vaccine Court has paid out more than $70 million to people making claims regarding Gardasil.”
“A new peer-reviewed study by researchers Joseph Hickey, Ph.D., and Denis Rancourt, Ph.D., re-examined the mathematical models used to justify policies that barred unvaccinated people from public venues. They found the models were based on the application of flawed mathematical risk models.
During the COVID-19 pandemic, politicians, scientists and media organizations vilified unvaccinated people, blaming them for prolonging the pandemic and advocating policies that barred “the unvaccinated” from public venues, businesses and their own workplaces.”
In a new research paper published in the journal Toxicology Reports, author Neil Z. Miller found that out of a total of 2,605 infant deaths reported to VAERS between 1990 and 2019, 58% occurred within three days of vaccination, and 78% occurred within seven days of vaccination.
In a new research paper published in the journal Toxicology Reports, author Neil Z. Miller reports on the relationship between sudden infant death syndrome (SIDS) death and the timing of vaccination, based on the Center for Disease Control and Prevention’s (CDC) Vaccine Adverse Events Reporting System (VAERS) database.
SIDS is defined as the sudden and unexpected death of an infant that remains unexplained after a thorough investigation. Although there are no specific symptoms associated with SIDS, an autopsy often reveals congestion and edema of the lungs and inflammatory changes in the respiratory system, according to the National Center for Health Statistics Vital Statistics of the United States 1988, Volume II, Mortality, Part A, Public Health Service, 1991.
Prior to contemporary vaccination programs, SIDS — sometimes referred to as “crib death” — was so infrequent it was not mentioned in infant mortality statistics.
After the national immunization campaigns were initiated in the U.S. in the 1960s, for the first time in history, most U.S. infants were required to receive several doses of DPT, polio, measles, mumps and rubella vaccines.
As Miller points out in his article, the ICD category for vaccine-related death, or cause of death as “prophylactic inoculation and vaccination,” was eliminated when the ICD was revised in 1979 — despite the fact that this information would be useful in trying to understand the relationship between vaccination and death.
But Miller, a medical research journalist and the director of the Thinktwice Global Vaccine Institute, provides an alternative route for establishing such a correlation — by observing the temporal relationship between vaccines and reported infant deaths, including SIDS deaths, in the CDC’s VAERS database.
Miller found that out of a total of 2,605 infant deaths reported to VAERS from 1990 through 2019, the majority “clustered” in close temporal proximity to vaccination — 58% occurred within three days of vaccination, and 78% occurred within seven days of vaccination.
Miller found the excess deaths within these ranges were statistically significant (p<0.00001), meaning the chance that this result is random is less than 0.001%.
The same type of clustering was present in the 1,048 reports of infant deaths (out of the total 2,605) reported to VAERS specifically as SIDS.
According to Miller, if there were no correlation between vaccination and infant deaths, one would expect to see an even spacing of deaths within the time range reported prior to vaccination —- not a clustering of deaths as Miller found.
Miller included a comprehensive literature review in his paper refuting the “official” claim that the SIDS epidemic was curtailed by having infants sleep on their backs — as recommended by the “Back to Sleep” campaign, initiated in 1992 by the American Academy of Pediatrics.
The subsequent rate of SIDS dropped by an annual average of 8.6% between 1992 and 2001. However, the neonatal mortality rate due to “suffocation in bed” increased during that same time at an average annual rate of 11.2%.
Other similar causes of infant death also increased significantly during this period, as reported by Miller. Further, from 1999 through 2015, the U.S. SIDS rate declined 35.8%. while infant deaths due to accidental suffocation increased 183.8 %.
Miller also affirms his main results from the paper (i.e., the temporal clustering of SIDS deaths with vaccination) through the discussion of seven additional peer-reviewed studies and two confidential reports.
On average, these authors found that substantial proportions of infant deaths occurred within one day (mean = 25%), three days (mean = 49%) and seven days (mean = 71%) post-vaccination, matching the results of the present study.
Mechanistically, vaccine injury has been tied to SIDS multiple times. Matturri et al. (2014) examined 13 SIDS deaths occurring within seven days of a hexavalent vaccine. Analysis of the brainstem and cerebellum of the deceased infants showed brain edema and congestion in all victims.
The authors hypothesized that “several compounds and immuno-potentiation adjuvants of the hexavalent vaccine might easily go beyond the blood-brain barrier, which in the first year of life is still immature and quite permeable, inducing neuronal molecular alterations in DNA, RNA and proteins of brainstem neurons regulating vital functions, with consequent fatal disorganization of respiratory control in particularly predisposed infants.”
Specifically, these authors implicated aluminum-based adjuvants in the dysregulation of respiratory control.
Scheibner and Karlsson (1991) monitored infant breathing during sleep before and after the DPT vaccination, revealing an increase in episodes where breathing nearly ceased or stopped completely. These episodes, which continued for several weeks post-vaccination, were not seen prior to vaccination.
Despite the official insistence that SIDS deaths are not caused by vaccination, as Miller points out, the National Vaccine Injury Compensation (NVICP) is set up to compensate families of individuals who are injured and/or die from vaccine administration.
Death from vaccination is compensated with $250,000 for “pain and suffering” to family members of the deceased victim. Conditions typically leading to death that are considered “table injuries” to be compensated under the NVICP include anaphylaxis and encephalopathy or encephalitis.
‘Healthy babies just don’t die for no apparent reason’
Kari Bundy, who lost her son after his four-month vaccinations, said she’s always been “flabbergasted” at the denial of the medical community of the link between SIDS and vaccines. “For me, it was too obvious to even attempt to ignore,” Bundy said.
Bundy lost her third-born child, Mason, in 2011.
“A few days after his routine four-month vaccinations, my husband and I discovered his dead body in the middle of the night, laying on his side, his body still warm,” Bundy said
Mason’s autopsy came back “unremarkable,” aside from some thymic petechiae, which is the most common gross finding in SIDS cases at autopsy.
“I was assured time and time again that he had not suffocated,” Bundy said.
When Mason died, Bundy learned if you can’t pay for a funeral, you can’t have one. So a few months after Mason’s death, she founded a nonprofit called Mason’s Cause, to provide grants to cover funeral costs for families who had experienced the loss of a child under the age of 1.
“I never wanted any parent to experience this devastating loss and not be able to bury their child,” Bundy said. She continued running the charity for just under 2 years, during which time she worked with 94 different families who experienced the death of a child under age 1.
Of those 94 infant deaths, 87 died from SIDS, or from causes “unknown.” Of the SIDS cases, 81 — or 93% — died within seven days of routine vaccinations.
“When I realized SIDS seemed to be undeniably related to vaccines, I realized I could no longer dedicate my life to running a charity that would help bury babies,” Bundy said. “That’s when I realized I wanted to save babies by speaking out about the real risks of vaccination.”
Bundy, who works for Children’s Health Defense as translations coordinator, said she’s grateful for research like Miller’s because it shows what she and all SIDS parents already knew — healthy babies don’t just die for no apparent reason.
PMSF, a nerve agent, is used to manufacture HPV vaccines, but it is not supposed to be in the final product. However, new research documents its presence in Merck’s Gardasil and Gardasil 9 HPV vaccines.
A new peer-reviewed study, “The Expanding Cocktail of Harmful Ingredients in Human Papillomavirus Vaccines,” by Brawer, A.E. and Sullivan, D.H., documents the presence of undisclosed, highly toxic volatile organic chemicals called AEBSF (aminoethyl benzenesulfonyl fluoride) and PMSF (phenylmethylsulfonyl fluoride) in Merck’s two HPV vaccines — Gardasil and Gardasil 9.
PMSF, also known as toluene, is a serine protease/acetylcholinesterase inhibitor, which means it can act as a nerve agent to inactivate central nervous system functions. When PMSF blocks the enzyme acetylcholinesterase, the result can be uncontrollable firing of motor signals which can manifest as seizures or other biochemical or physiological disorders. PMSF has been used as a nerve agent in biological warfare.
PMSF and AEBSF are used to manufacture HPV vaccines, but are not supposed to be in the final product and therefore do not have to be listed as ingredients.
However, this new study documents that these toxic organic chemicals are in the final vaccine product and likely initiate the onset of a host of serious adverse events that have been reported following HPV inoculations.
Such outcomes include cardiovascular events, motor neuron disorders, autoimmune disorders, cognitive and mood disorders, neurological disorders, gastrointestinal disorders, miscarriages, menstrual disorders, seizures, headaches, extreme fatigue, skin disorders, sleep disorders, paralysis, encephalitis — and even sudden death.
Since these toxic chemicals are not publicly disclosed and are not listed in the package insert, how was it discovered that they are used in the manufacturing process and that they are, in fact, in the final product?
It was first discovered by a mother, Elizabeth O. Schneider, whose son, John, suffered severe adverse reactions as an infant after receiving the Hepatitis B vaccine, Engerix B, in 1993. Schneider was driven to find out what happened to her infant son.
In 1995, Schneider used the Freedom of Information Act to obtain a transcript of the 1988 U.S. Food and Drug Administration (FDA) Advisory Committee meeting at which the Engerix hepatitis B vaccine was approved. Though a lot of information in the transcript was redacted, the identity and use of PMSF was not — prompting Schneider to find out more about the chemical.
After a lengthy process, Schneider obtained patent information for Engerix B, a genetically engineered, recombinant vaccine. The patent (Wijnendaele, et.al. U.S. Patent Document 4,857,317, Aug. 15,1989) indicated that PMSF was used in the extraction and purification of proteins from the yeast culture producing them.
In a 1985 publication by the Center for Drugs and Biologics, the FDA clearly expressed concern about the use and removal of PMSF and other protein derivatizing chemicals “which may lead to undesirable immune responses in recipients of the final product.”
When Schneider further researched the known adverse effects of PMSF (toluene), she discovered that all of the injuries her son experienced were associated with PMSF toxicity. She also learned that the chemical could not be eliminated by people who lack certain drug metabolizing enzymes in the CYP450 pathway.
Her son was such a person. However, Schneider could not move forward with her case because she did not have the resources to analyze vials of Engerix B nor the availability of medical experts to explain the mechanism by which PMSF would get into the final product.
Fast forward to 2006, when Gardasil, another recombinant vaccine with a patent similar to Hepatitis B, was licensed. Schneider obtained patent information (Jansen, et.al. U.S.Patent Document 5,888,516. March 30,1999) for Gardasil and saw that PMSF was similarly used in the manufacturing process.
Schneider was horrified to see again, following Gardasil inoculations, a multitude of reported serious adverse events which were consistent with known side effects of PMSF.
One victim of Gardasil vaccine side effects was this writer’s daughter, Christina Tarsell, who died 18 days after her third Gardasil injection.
Eager to share her hundreds of pages of research to try to help Gardasil victims, Schneider forwarded the information to me. The evidence was compelling. The government conceded that Christina Tarsell died as a result of her Gardasil vaccinations, based on a somewhat different causal mechanism.
Nevertheless, I continued to pursue qualified researchers to investigate the PMSF theory.
Finally in 2018, Deborah Sullivan, a registered nurse and researcher, was similarly convinced that the theory was highly plausible and likely causally related to the adverse outcomes reported for HPV vaccines. Advancing the theory, however, would require evidence that PMSF and AEBSF are in the final product as well as a science-based explanation as to how they got there
Sullivan vigorously and relentlessly explored the issue further. As a nurse, she had experience observing and treating youth with severe adverse symptoms post-Gardasil vaccination and could confirm that those she investigated had deficiencies in the CYP450 pathway.
Sullivan also had online access to relevant research publications. Among them, she found one documenting how organic solvents like PMSF are readily absorbed by silicones. This prompted her to contact Dr. Arthur E. Brawer, a well known physician and researcher with expertise in rheumatology and silicone toxicity. Brawer’s research has shown that silicones “are hidden toxic ingredients in Gardasil vaccines.”
Through their collaboration, Sullivan and Brawer confirmed the presence of PMSF in Gardasil and Gardasil 9. They also found an explanation for how these volatile organic solvents ended up in Gardasil’s HPV vaccines.
The results of the findings published in this paper break new ground for further research, which we hope will lead to the removal of dangerous HPV vaccines from the market as well as to treatments and justice for the victims.
“After my son was injured in 1980 by the crude, toxic whole cell pertussis vaccine in DPT shots, I joined with other parents of DPT vaccine injured children in 1982 to establish the charity known today as the National Vaccine Information Center (NVIC) with the mission of preventing vaccine injuries and deaths through public education. We have defended the legal right to make voluntary decisions about vaccination for 41 years.
Since then, I have watched the Public Health Empire grow and use “no exceptions” vaccination laws as the tip of the spear in the great culture war gripping this and other nations around the world. It is an ideological and political war that has been going on since the 19th century, pitting those who believe in the right to autonomy and liberty against those who believe in centralized, authoritarian government control. How it ends will define what freedom means for human populations around the world during this and many centuries to come.”
Our governments should be protecting our children, and independent studies into the vaccination program are long overdue. The reason they will not tackle this hot potato is purely financial: It could cost billions in compensation and could potentially bankrupt countries.
We are constantly told by our health authorities that childhood vaccinations help train young immune systems and that vaccinated children are healthier than unvaccinated.
How do governments know this? They don’t. It is pure supposition. They have no definitive proof because of a lack of double-blind placebo-controlled trials and no official vax versus unvaxxed studies.
But more than 100 official papers do exist and they do not support government assertions. Vaccinated children suffer higher levels of chronic illness and autoimmune disease than unvaccinated children.
Brian Hooker, Ph.D., is co-author of a book that looks at all those papers. He is professor emeritus of biology at Simpson University in Redding, California, and like most parents, he believed in childhood vaccination until his 15-month-old son was injured by three vaccines: diphtheria, tetanus and pertussis (DTaP), oral polio and haemophilus influenzae type b (HIB).
“He had an ear infection at the time and should not have received the vaccines, but the doctor said it was fine,” said Hooker. “He lost eye contact, was unable to walk unaided and he never recovered.”
And yes, he did go on to get the measles, mumps and rubella (MMR) vaccine because the doctors did not make the association between his son’s regression and the vaccines, and neither had Hooker. His son is now 25, non-verbal, has gastrointestinal problems, mitochondrial dysfunction and is diagnosed with autism. There is no cure.
For 25 years, Hooker, who also has a degree in chemical engineering, has campaigned for recognition of vaccine injury and thought he would get somewhere in 2014 after the Centers for Disease Control and Prevention’s (CDC) epidemiologist and senior researcher Dr. William Thompson sent him a study that showed a correlation between autism, the MMR and African American boys.
It was a study Thompson sat on for 10 years before it was released. It showed that African American children who received the MMR before they reached 36 months had 2.4 times greater odds of an autism diagnosis compared with children receiving the MMR after 36 months.
It should have been a huge red flag but had no major impact and was not widely reported in mainstream media, although President Donald Trump wanted to create a Vaccine Safety Commission to conduct these studies. However, he accepted $1 million from Pfizer for his inauguration and unsurprisingly, the Vaccine Safety Commission was shot down before it was even formed.
For 38 years, Dr. Anthony Fauci was head of the U.S. National Institute of Allergy and Infectious Diseases. He has been a barrier to vax vs unvaxxed studies and claimed that double-blind placebo-controlled vaccine trials that had been conducted contained all the evidence needed.
When challenged by lawyers Robert F. Kennedy Jr. (now running for president) and Aaron Siri in 2017, on behalf of Del Bigtree, the presenter and vaccine injury campaigner who created the Informed Consent Action Network, Fauci said he would send the evidence. It never materialized so they sent a legal demand.
Many vaccines have long-term health impacts that do not become evident for years. In a 1999 interview, Fauci acknowledged that many severe injuries would remain hidden, and if the agency rushed vaccines to approval “then you find out that it takes 12 years for all hell to break loose, and then what have you done?”
American children receive 71 vaccination doses, and the heads of the vaccine program were unable to produce any double-blind placebo-controlled trial to support their safety.
The CDC says that 1 in 36 children has a diagnosis of autism and the numbers are similar in the U.K., but no one has identified a cause.
A shocking fact is that when vaccine manufacturers create a childhood vaccine, they do not use saline for the control group. They will either use a different vaccine, a different version of the vaccine they are testing or an adjuvant.
For example, neurotoxic, amorphous aluminum hydroxyphosphate sulphate, or AAHS, an adjuvant, was used as a control in the human papillomavirus (HPV) Gardasil trial with devastating results.
Governments justify this by saying that adverse events are only “one in a million.” This figure is quoted by all Western countries with vaccine programs but how have they come to it?
The U.S. government compares the number of vaccine injuries compensated by the National Vaccine Injury Compensation Program with the total number of vaccines given in the U.S. Most vaccine-injured people have no idea about the scheme and doctors rarely correlate vaccination injury to the onset of debilitating symptoms.
Most doctors deny it exists. In the U.K., people can apply to the Vaccine Damage Payment Scheme, but most do not know about this either. The scheme is restrictive, a claimant must prove 60% disability caused by vaccines with a small one-off payment of 120,000 euros if successful.
The truth will always be out and Hooker and his friend RFK Jr. have found elusive, but official, vax vs unvaxxed publications hidden in the National Institutes of Health archive in the global research database PubMed.
Hooker said: “We have so far identified over 100 peer-reviewed articles from open, peer-reviewed, scientific, and medical literature.”
Here are the results from just two, but without fail the book’s studies show that vaccinated children fare worse when it comes to robust health. The numbers differ slightly, which is to be expected, but unvaccinated children are in the bottom percentile.
A particularly shocking finding in the following study is that no unvaccinated children suffer from attention-deficit/hyperactivity disorder (ADHD) compared with 5.3% of the vaccinated group.
In this powerful paper, they took a unique approach to investigating the vax versus unvaxxed health differences of the children in Thomas’ medical practice. Rather than examining whether children had been diagnosed with the disorders studied, they compared the number of office visits associated with specific diagnoses in vax versus unvaxxed children.
Lyons-Weiler wrote: “Our measure, the Relative Incidence of Office Visits (RIOV), is sensitive to the severity of disease and disorder — specifically, the disease burden.”
RIOV also reflects the frequency of recurring diseases such as fever, ear infections and respiratory infections.
They compared 2,763 fully and partially vaccinated children with 561 unvaccinated children.
The vaccinated children had significantly more office visits associated with ear infections, conjunctivitis, breathing issues, anemia, eczema, behavioral issues, gastroenteritis, weight and eating disorders and respiratory infections than the unvaccinated children, although unvaccinated children experienced more chickenpox and pertussis (whooping cough).
Due to the meager rates of certain conditions in Thomas’ practice, such as developmental disorders, the researchers could not determine statistically significant differences between the two groups. However, the ADHD figures were significant, 5.3% vaccinated compared with zero unvaccinated.
The study was published in November 2020 in the International Journal of Environmental Research and Public Health which then came under pressure to retract it, which it did.
The retraction statement included a brief, vague explanation: “Following publication, concerns were brought to the attention of the editorial office regarding the validity conclusions of the published research.”
Below are the graphs from the study.
The other example study considered in this article is Analysis of Health Outcomes in Vaccinated and Unvaccinated Children: Developmental Delays, Asthma, Ear Infections and Gastrointestinal Disorders conducted by Hooker and medical research journalist Neil Miller and published in the journal SAGE Open Medicine in 2020.
They examined the medical records from three different pediatric practices in the U.S. They followed 2,047 patients from birth to a minimum age of three years, and a maximum age of 12.5 years.
They divided the children into two groups: those who received any vaccines before their first birthday (69.1%) and those who did not (30.9%). The authors accounted for diagnoses only after a child’s first birthday to establish that vaccination preceded the first diagnosis of illness or disorder.
As shown in Figure 2.4, vaccinated children were diagnosed with developmental delays at 2.18 times greater odds, asthma at 4.49 times greater odds and ear infections at 2.13 times greater odds than unvaccinated children. These odds ratios were statistically significant.
Breastfeeding provided protection against a child developing asthma but not as much as for breastfed and unvaccinated babies. For example, unvaccinated babies who were bottle-fed were 5.4 times more likely to develop asthma than unvaccinated breastfed babies. Vaccinated and breastfed babies were 10.7 times more likely to develop asthma while vaccinated and bottle-fed babies were 23.8 times more likely to develop asthma.
Our governments should be protecting our children, and independent studies into the vaccination program are long overdue.
The reason they will not tackle this hot potato is purely financial: It could cost billions in compensation and could potentially bankrupt countries. So it is up to parents to ask questions, research and protect their children.
Sally Beck is a freelance journalist with 30 years of experience in writing for national newspapers and magazines. She has reported on vaccines since the controversy began with the MMR vaccine in 1998.
The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children’s Health Defense.
“Fueled by the phrase, “pandemic of the unvaccinated,” last year many corporate media outlets began running a series of articles attacking people who chose to exercise their medical informed consent rights and not get vaccinated for COVID-19. The hit pieces laid the blame for the continuing COVID pandemic squarely on the shoulders of unvaccinated Americans.”