For the last few years, I have been telling people that the British “Royal Family” are absolutely not as they seem. […] I have said that these people are absolutely not British in any aspect, but are criminals, frauds, and have absolutely no rights to the British throne at all..
Now, I want to reveal through an article from my friend, Whitewraithe, who writes the blog: Pragmatic Witness, that amazing article, entitled: “Britain’s Jewish Royal Family” right here for everyone to see for themselves, and I do, of course, have some additional thoughts and comments to follow:
Britain’s Jewish Royal Family
What we have been sold is no less than the groundwork for the imposition of a future Jewish Monarchy in Great Britain. And engineered by the House of Rothschild, whose relations and puppets on Wall Street and in the City of London are responsible for a deliberately created international financial crisis aimed at creating a one world currency system, a one world bank and a New World Order, one world government.
As one Royal insider commented “An insecure immigrant Royal family who have never felt at ease with the British people, and always more secure with immigrants and outsiders, and an alliance with the richest Jewish family in the world, heads of what is increasingly being re-Christened “The Jew World Order, who also seek to raise their status, is perceived by the Queen and the Duke of Edinburgh as the best guarantor of their family’s future and safety. In short, we will one day see a Rothschild Royal family.”
Many people still cannot get Kate Middleton or why she, a supposed ‘commoner’ would marry Prince William. But hidden right under our noses is the truth the controlled mainstream media is hiding. Kate Middleton is a Jew from a maternal line of non-practicing, assimilated and poor Sephardic Jews aligned to the Church of England. Her mother whose maiden name is Goldsmith, practicing or not, is Jewish and under Jewish law if the mother is Jewish then the children are Jewish, therefore the children of Prince William will be legally Jewish….especially as William, under Judaic law, is also a Jew!
Under Jewish law if William and Kate have children their children will be Jews!
In Tina Brown’s book ‘The Diana Chronicles’, the author claims that Princess Diana’s Jewish mother Frances Shand Kydd had a long-running affair with Sir James Goldsmith during her marriage to Earl Spencer. She suggests that Diana, who was born in 1961, was Goldsmith’s love child and not Spencer’s daughter. Even so the father’s line is irrelevant as Jewishness travels down the matriarchal line and Diana’s mother was a Jew. See also: The Times of Israel — Will the Future King of England Be Jewish?
The Goldschmidts, like their neighbors and relatives, the Rothschilds, had been prosperous merchant bankers in Frankfurt, Germany since the 16th century.(Wikipedia). In 1773, Mayer Rothschild invited Goldschmidt, (Goldsmith), Schiff, Oppenheimer, Warburg and eight other ambitious Jewish businessmen to his goldsmith shop. Together they formulated a long term plan […].
PRINCESS DIANA’S JEWISH SON AND FUTURE KING WILLIAM.
The original and current Jewish definition of a “born Jew” is a person whose mother is Jewish. Judaism is passed down in a matriarchal lineage. Prince William’s mother, Princess Diana, had a Jewish mother (Frances Ruth Burke Roche; a Rothschild) and she likely had a Jewish father (though his lineage would be irrelevant under Jewish law). That would make William – Jewish.
PRINCESS DIANA’S JEWISH HALF-BROTHERS
Diana shares a striking physical resemblance to the children of Sir James Goldsmith – Zak Goldsmith, Ben Goldsmith and Jemima Goldsmith. They are allegedly Diana’s half brothers and sister.
Following the Rothschild protocol of interbreeding to keep the power and wealth all-in-the-family, Diana’s alleged half brother Ben Goldsmith wed Kate Rothschild in 2003.
Princess Diana’s other alleged half brother, Zac Goldsmith, divorced his wife after he was elected British MP. He is now living with Alice Rothschild. This Rothschild-Goldsmith couple is also expected to marry.
Many people were perplexed why parliament should — recently, during one of it’s most busy sessions since the war –, have enacted a law allowing Catholics to ascend to the throne. What perplexed them was that the issue was not even on the horizon and there was simply no justification at that stage to use valuable parliamentary time dealing with it. In the light of this theory we can better speculate what was going on. This was an ‘en Passant’ means of allowing Jews to take the throne on the basis of the ‘equality’ and ‘diversity’ our cultural Marxist Queen so greatly cherishes.
People have also always been mystified why Charles married Diana in the first place given that he was deeply in love with and had a long-standing relationship with Camilla Parker-Bowles. But that marriage made perfect sense if the family simply wanted Jewish children for a future Jewish monarchy. Whether the relationship lasted or not was of little importance once the the children were born and how convenient that Diana went the way of a wife of Henry the Eighth.
But the Kate-William marriage also perhaps explains Prince Charles’s dictum that, should he be ruler, he would seek a constitutional change that would remove him from sole governance of the Church of England to become the leader “Of all faiths.” Such a constitutional move would give Judaism parity with Christianity allowing a Jewish member of the Royal Family, for example, even if it were a woman, to ascend to the throne […].
And so the Rothschilds attended the royal wedding in more ways than one!
THE PLAN WAS THERE ALL ALONG, IN FRONT OF OUR UNCRITICAL, BRAINWASHED EYES
COMING OF THE MESSIAH.
However, the Talmud states that the leader of the world Jewish takeover would be a King, meaning that, should a male Jew ascend to the throne, such a King would then himself not only be the senior Elder of Zion but also the long awaited Messiah; The King of the Jews. As there are no remnants of the ancient Jewish royalty, and in order to fulfill the prophesy, Jewish royalty must be re-established, and it appears from this evidence that the current British Royal family has become the vehicle of choice.
At last, we come to understand the old Masonic claim that “Jerusalem will be rebuilded here, in England’s green and pleasant land.” The King of the Jews will rule the world from London where the ‘square mile’ of London City no longer belongs to the English people but was long ago sold to the Jews. His castle may well sit on the site of the last Olympic games; an area stolen by the state from the East Londoners who lived and worked there, perhaps in the long term for this very purpose.
Could the New Jerusalem be built in the ‘square-mile’ or could it be built on the Olympic site which was surrounded during the event by the Jewish and Masonic symbol of triangular, pyramid floodlights? Could the arena of the Olympic stadium become the site for the rebuilding of the temple? […]
On a related point, Royal rumour has it that Prince Harry was under great pressure, especially from the Queen, to marry Meghan Markle to help promote the racial genocide of the indigenous British people through mass immigration, cultural Marxism and Zioncorp promoted miscegenation.
A series of Jewish and far-left MPs such as Margaret Hodge, using mass third world immigration and fixed housing lists in the East End, have already succeeded in almost wiping out the Cockneys in this effort.
The Queen famously threatened in her 2010 Christmas Speech “The future face of Britain is the face of the Commonwealth.”
i.e.: The end of the white race in the United Kingdom!
Across the country, frenzied legislators are responding to the pharmaceutical industry’s orchestrated fear campaign around measles by seeking to impose further mandating of Merck’s measles, mumps and rubella (MMR) vaccine. Although ongoing mumps outbreaks involving thousands of at-risk adolescents and young adults completely dwarf the number of measles cases, no one is covering the mumps story—because it will expose the fact that Merck has been in court for over eight years due to scientists blowing the whistle on Merck’s fabrication and falsification of the effectiveness of the mumps component of its MMR vaccine. Instead of punishing Merck for its chicanery, legislatures are rewarding the company by making it impossible to refuse Merck’s profitable vaccine, subjecting a generation of American children to the risk of serious complications from mumps infection at an age that nature never intended.
When younger children experience mumps, the virus is relatively harmless; infected children often exhibit no symptoms. When mumps strikes adolescents or adults, on the other hand, the infection can cause far more serious adverse effects, including inflammation of various organs (brain, pancreas, ovaries and testicles)—as well as damage to male fertility.
Inflammation of one or both testicles (a condition called orchitis) occurs in approximately one in three post-pubertal men who get mumps and can contribute to sperm defects and subfertility as well as impairing the function of cells that produce testosterone. An estimated 30% to 87% of men with bilateral orchitis induced by mumps experience full-blown infertility—a major cause for concern given the significant declines in male fertility observed over the past several decades. Thus, it appears that Merck’s vaccine, instead of protecting children, not only delays onset of disease to later age cohorts but has the potential to cause serious and permanent injury.
Merck and mumps vaccines
Let’s look at a quick history of mumps and MMR vaccination in the United States. The Food and Drug Administration (FDA) licensed Merck’s initial mumps-only vaccine in 1967. In 1971, Merckintroduced its first combination MMR vaccine, followed by the MMR-II vaccine in 1978 (which repurposed the rubella component) and the MMR-plus-varicella (MMRV) ProQuad vaccine in 2005. Since the initial 1967 vaccine, Merck has enjoyed a unique monopoly position in the U.S. market for mumps and MMR vaccines, with combined sales of MMR-II and ProQuad bringing in over $720 million in 2014 alone. Merck consistently places in the top five pharmaceutical companies globally, and the market valued its stocks at a seven-year high as of late 2018.… Merck has willfully and illegally maintained its monopoly through ongoing manipulation and by representing to the public and government agencies a falsely inflated efficacy rate for its Mumps Vaccine.
In order to score the lucrative MMR monopoly, Merck needed to satisfy the FDA that all three components of the combination vaccine could achieve 95% efficacy, but the mumps portion was bedeviling. In fact, as alleged in a lawsuit filed by two senior Merck scientists in 2010 under the False Claims Act, the company has known since the late 1990s that the mumps component of the MMR is “far less” than 95% effective. A 2005 study published in Vaccine estimated the effectiveness of mumps vaccination to be closer to 69%, and the authors noted that their results were consistent with other studies.
The two whistleblowers assert in the lawsuit—which is reportedly headed to trial sometime this year—that Merck has “willfully and illegally maintained its monopoly” through “ongoing manipulation” and by “representing to the public and government agencies a falsely inflated efficacy rate for its Mumps Vaccine.” Specifically, the two scientists claim that Merck executives ordered them to use “rigged” methodologies, including taking antibodies from rabbits and adding them to human blood vials, in order to gull regulators into assuming an antibody response robust and durable enough to merit licensing. When those “enhanced” tactics did not achieve Merck’s “fabricated [95%] efficacy rate,” the whistleblowers allege, the company resorted to simply falsifying the test data and engaging in other fraudulent activities.The fact that we have mumps showing up in highly immunized populations likely reflects something about the effectiveness of the vaccine.
Unprotected adolescents and young adults
The poor performance of the MMR’s mumps component and the doubtful “durability” of mumps-specific immunity following vaccination are of concern. In fact, we are already living with the legacy of this badly flawed vaccine. Rather than protecting a generation of American children from mumps infection in childhood, the vaccine has merely postponed the onset of the virus to older age groups, putting them at much greater risk. Researchers confirm an increase in the median age of mumps patients, a surge in the size and number of mumps outbreaks in highly vaccinated populations and higher rates of complications—including orchitis.
Across the country, galloping mumps epidemics have been ravishing an older generation of vaccinated individuals. The Centers for Disease Control and Prevention (CDC) reported 150 outbreaks (9,200 cases) in the year and a half from January 2016 to June 2017, affecting “schools, universities, athletics teams and facilities, church groups, workplaces, and large parties and events.”
Over the past several years, the number of college campuses reporting mumps outbreaks has exploded—at institutions ranging from Harvard and Temple to Syracuse, Louisiana State and Indiana universities. At the University of Missouri, which in 2016 reported 193 mumps cases on campus, the health center director reported not having seen anything like it “in her 31 years at the school.” Commenting on the fact that all of the afflicted students had had the requisite two doses of MMR, she noted,
“The fact that we have mumps showing up in highly immunized populations likely reflects something about the effectiveness of the vaccine.”
The mumps virus has also made a “comeback” in other settings where younger adults congregate. For example, a naval ship deployed to the Persian Gulf, the USS Fort McHenry, has been unable to come ashore since early January because of a mumps contagion that has devastated its crew—even though the military vaccinates all personnel against the virus and despite the Navy having immediately subjected the crew in question to another MMR booster. News accounts have declined to comment on mumps complications but describe the quarantine as “a morale killer” for crew members who are accustomed to having monthly port calls. Infection control protocols stipulate that the Navy cannot declare the situation “under control” until “50 days after the last affected service member recovers.”
Endangering rather than protecting youth
All of these cohorts are part of an age group that should never get mumps. As Children’s Health Defense recently noted, whereas “flares of illness in vaccinated groups should prompt some serious questions about vaccine failure,” legislators and government agencies “are displaying a dangerous indifference to vaccination’s unintended consequences.” Dancing to puppet strings manipulated by Merck, legislators across the country are trying to foist even harsher MMR mandates on unwilling Americans, dooming a generation of children to the serious risks of late-onset mumps infections.
Part II
It has been about five decades since the U.S. Food and Drug Administration (FDA) approved Merck’s first mumps vaccine. The company began launching combination MMR (measles, mumps and rubella) vaccines in the 1970s. Coincidentally—or not—an infertility crisis has been brewing over roughly the same time period, with dramatic declines in sperm counts and record-lowfertility levels. However, few investigators seem interested in assessing whether mumps outbreaks in highly vaccinated populations of teens and young adults could be having long-termeffects on fertility or other health indicators.
As described in Part I, childhood MMR vaccination has been an unmitigated disaster where mumps is concerned, deferring mumps infection to older ages and leaving adolescents and young adults vulnerable to serious reproductive complications. Public health reports show that the vast majority of mumps cases and outbreaks occur in youth who have been fully vaccinatedwith the prescribed two-dose MMR series, supporting a hypothesis of “waning immunity after the second dose.” FDA and Centers for Disease Control and Prevention (CDC) officials even admitthat mumps outbreaks in the post-vaccination era “typically involve young adults,” and that vaccination is failing to protect those who are college-age and above.
Myopically, many vaccine experts have called for a third MMR dose—or even “booster dosing throughout adulthood”—even though the FDA’s and CDC’s own research shows that MMR boosters in college-age youth barely last one year. As alleged in whistleblower lawsuits wending their way through the courts over the past eight years, Merck presented the FDA with a “falsely inflated efficacy rate” for the MMR’s mumps component, using animal antibodies and other fraudulent tactics to fool FDA—and the public—into believing that the vaccine was effective.
When infection arises after puberty, however, mumps is no laughing matter, presenting an increased risk of complications such as hearing loss, encephalitis and inflammation of the reproductive organs.
Mumps after puberty is no laughing matter
Around the time that the first mumps vaccine came on the market, the 1967 children’s classic The Great Brain humorously depicted mumps infection in childhood as a mere nuisance. The book’s young protagonist goes out of his way to intentionally infect himself with mumps so that he can beat his two brothers to the recovery finish line—and he experiences no adverse consequences other than his siblings’ annoyance.
When infection arises after puberty, however, mumps is no laughing matter, presenting an increased risk of complications such as hearing loss, encephalitis and inflammation of the reproductive organs. About one in three postpubertal men with mumps develops orchitis(inflammation of the testes), which can damage sperm, affect testosterone production and contribute to subfertility and infertility. During a mumps outbreak in England in the mid-2000s, mumps orchitis accounted for 42% of all hospitalized mumps cases; the researchers attributed this outcome—which was the most common reason for hospitalization—to “the high attack rates in adolescents and young adults” that occurred “despite high coverage with two-dose MMR.” An analysis of a 2006 mumps outbreak in the U.S. reported that male patients were over three times more likely than female patients to experience complications, “due primarily to orchitis.”
An estimated 5% to 10% of postpubertal women will develop oophoritis (swelling of the ovaries) following mumps infection. Oophoritis is associated with premature menopause and infertility, but mumps-related oophoritis has garnered little notice.
Mumps infections are often asymptomatic or produce nonspecific symptoms such as fever, while cases of orchitis may present with no other mumps symptoms. Nonetheless, public health officials advise clinicians that orchitis is an instant cue to test for mumps virus, and testing often reveals elevated mumps antibodies. In a case report of MMR failure, British clinicians isolated a novel genetic strain of mumps virus from the patient’s semen two weeks after the onset of orchitis and found mumps RNA in the semen 40 days later; they also noted “the appearance of anti-sperm antibodies,” with “potential long-term adverse effects on the patient’s fertility.”
In 2017, researchers who reviewed 185 studies conducted in Western nations found that sperm counts had plummeted by 50% to 60% between 1973 and 2011—an average decrease of 1.4% annually. Commenting on this work, one analyst estimated that 20% to 30% of young men in Europe and North America have sperm concentrations associated with a reduced ability to father a child. Given estimates that as much as 40% of reproductive problems have to do with the male partner, there is agreement on the importance of “finding and eliminating [the] hidden culprits in the environment” that most researchers believe are to blame.
An estimated 5% to 10% of postpubertal women will develop oophoritis (swelling of the ovaries) following mumps infection. Oophoritis is associated with premature menopause and infertility, but mumps-related oophoritis has garnered little notice.
MMR’s and MMRV’s potential to impair fertility never studied
Merck has not evaluated either of its two MMR vaccines—the MMR-II and the MMR-plus-varicella (MMRV) vaccine—for their potential to impair fertility. Whether such testing would unearth direct effects on fertility (as appears to be possible with HPV vaccination in women) is thus unknown. However, mumps vaccination undeniably increases reproductive-age individuals’ risk of mumps infection and, in the process, increases the risk of fertility-altering complications. These facts alone should be attracting far more attention.
Unfortunately, because clinicians already tend to underdiagnose mumps infection and underestimate mumps complications, it is likely that they are failing to recognize possible vaccine-induced reproductive health consequences of mumps infection in their adolescent and young adult patients. In one university outbreak, “most physicians…did not suspect mumps,” and even when they became aware of the outbreak, “diagnosing mumps was not always straightforward.” Moreover, although differentiating between vaccine strains of mumps virus and wild types could provide valuable information, few clinicians have the capacity or inclination to perform testing of this type. A Japanese study of cerebrospinal fluid and saliva from patients with mumps complications found vaccine strain in nearly all of the samples and noted the information’s importance in helping determine whether the complications were vaccine-related.
Those who have sought to understand mumps vaccines’ poor performance point to a mixture of explanatory factors. These include waning immunity, the high population density and close quarters encountered in settings such as college campuses, incomplete vaccine-induced immunity to wild virus as well as viral evolution such that “the vaccine triggers a less potent reaction against today’s mumps viruses than those of 50 years ago.” However, some also quietly admit that individuals with “mild vaccine-modified disease” could be perpetuating the chain of transmission. This latter point ought to be raising questions about the logic and wisdom of administering further rounds of MMR boosters during outbreaks while ignoring the problems created by the doses already given.
… some individuals respond poorly to mumps vaccination and vaccine-induced antibody levels correlate poorly with protection from mumps infection, irrespective of the number of additional doses of mumps-containing vaccine they receive.
Most scientists appear to be either resigned to ongoing mumps outbreaks in vaccinated populations or actually accept periodic outbreaks as the cost of doing business. Publications by FDA and CDC researchers reveal these agencies’ awareness that some individuals respond poorly to mumps vaccination and that vaccine-induced antibody levels correlate poorly with protection from mumps infection, “irrespective of the number of additional doses of mumps-containing vaccine they receive.” Considering the effects on fertility, the generally abysmal track record of mumps vaccination and Merck’s fraudulent claims about efficacy, it is hard to fathom medical and public health experts’ complacency about current mumps vaccines and vaccine policies.
Entrance to the headquarters of the Centers for Disease Control and Prevention in Atlanta, Georgia
In the mainstream discourse about the subject of vaccines, one issue that is never directly raised is the right to informed consent. This right is one of the most fundamental ethics in medicine, and yet the government and media treat it as uniquely irrelevant when it comes to this one particular pharmaceutical product. The reality is that public vaccine policy subjects the entire population to a mass uncontrolled experiment, and legislation mandating their consumption constitutes a serious threat to both our health and our liberty. The major corporate media, for their part, have chosen to take on the role, in dutiful service to the state, of policy advocacy rather than journalism.
So let’s remedy that failure by taking a serious look at public vaccine policy in the context of the right to informed consent. (While focusing primarily on the US population, the information that follows also bears relevancy for other countries.)
The Inadequacy of Pre-Licensure Safety Trials
We’re supposed to believe that somehow the science is “settled” on vaccines. But that belief is preposterous. The reality is that there is endless debate and controversy about vaccines in the medical literature. The major corporate media don’t even begin to scratch the surface in their reporting on vaccines. There are countless serious issues related to vaccination that the public have no idea about because health officials and the media refuse to even touch them. The news media just repeat the same routine talking points in virtually every broadcast or article on the subject, spitting out misinformative propaganda instead of educational content.
One thing most people don’t know about vaccines—because they are told neither by public health officials, nor by the major media, nor by pediatricians or others working within the medical establishment—is that they aren’t held to the same standard as other pharmaceutical drugs when it comes to safety. We’re supposed to believe as gospel truth that vaccines recommended by the US Centers for Disease Control and Prevention (CDC) have been extensively studied and proven safe and effective. But that’s just not true. In fact, one significant difference between how the US Food and Drug Administration (FDA) regulates vaccines versus other drugs is that pharmaceutical companies are not actually required to conduct long-term, randomized, placebo-controlled studies to demonstrate their vaccine products’ safety for use in human populations.
Nor do they do so. This can be seen simply by going to the FDA’s website and examining the manufacturers’ package inserts for vaccines licensed for use in the US market.
These inserts are required by law to disclose adequate warnings to consumers about the benefits and risks of the vaccine. Failure to provide adequate warnings is one of only two conditions under which a vaccine manufacturer can be sued in civil court for harms caused by vaccination. The other is failure to manufacture the vaccine according to specifications. Apart from failing on either of those counts, vaccine manufacturers have total legal immunity against vaccine injury lawsuits, which the government granted to them under a 1986 law designed to preserve existing public vaccine policy in the face of threats to vaccine supply resulting from injury lawsuits that were putting vaccine manufacturers out of business.
The law, the National Childhood Vaccine Injury Act, also established the Vaccine Injury Compensation Program (VICP), which is funded by an excise tax on every vaccine dose administered and effectively shifts the financial burden for vaccine injuries away from the pharmaceutical industry and onto the taxpaying consumers.
As an example showing how proper safety studies are not required to gain FDA approval, take the Hepatitis B (HepB) vaccine. There are two brands that are licensed in the US for use in infants, and this vaccine is typically administered to newborn babies on the very first day of their lives. The CDC recommends this universally, even though the vast majority of babies are not at significant risk of infection. (The virus is transmitted by bodily fluids primarily through sex or injection drug users’ sharing of needles, so unless the mother or another close household contact is a carrier, infection of the infant is an improbability.) The CDC also recommends the vaccine to women during pregnancy. This is so despite the vaccine containing aluminum, which is used to provoke a stronger immune response, but which is also a known neurotoxin. Until it was phased out of most childhood vaccines starting in 1999, the HepB vaccine also contained a preservative called thimerosal, which by weight is half ethylmercury, another known neurotoxin that, like aluminum, crosses both the placental and blood-brain barriers and accumulates in the brain.
Neither of the two HepB vaccines on the market recommended for use in both newborns and pregnant women were studied to determine the safety of these practices. The two vaccines are Merck’s Recombivax B and GlaxoSmithKline’s Engerix-B. Both products’ package inserts state explicitly that “no adequate and well-controlled studies” have been done to evaluate the vaccine’s safety in pregnant women. Merck did include infants in three clinical trials, but it included them with older children up to 10 years of age, rendering the results uninterpretable with respect to the safety of vaccinating babies. Furthermore, the studies included only 147 children, had no placebo control group, and had a follow-up period of only five days. Hence, the trials could not possibly have detected any but the most frequently occurring and immediate-term adverse events. GSK’s trials were larger, including 5,071 subjects. But once again, infants were included with healthy adults and children, there was no placebo control group for comparison, and the follow-up period was just four days.
For another example, take the flu shot. Inactivated influenza vaccines are also recommended by the CDC for use in pregnant women, as well as infants as young as six months. Whereas it was removed from other vaccines routinely recommended for children, multi-dose vials of the influenza vaccine still contain mercury. As with the HepB vaccine, flu shot manufacturers disclose in their package inserts that safety and effectiveness of the vaccine have not been established in pregnant women. A systematic review of the literature in 2014 by the prestigious Cochrane Collaboration—an international organization specializing in this type of study, also called a meta-analysis—noted that the number of randomized controlled trials to determine the safety of vaccinating pregnant women was zero. A 2012 Cochrane meta-analysis found no good evidence that the flu shot is effective at preventing the flu in children under age three and “no usable data” on the safety of vaccinating children under two. Given the CDC’s recommendation for vaccinating infants as young as six months, the study authors stressed that studies to determine the safety and effectiveness of this practice are “urgently required”.
These and numerous other Cochrane reviews have also warned that many of the included studies were industry funded, and that industry funding has, unsurprisingly, been shown to bias results in favor of the products under study.
As a 2012 review published in the American Journal of Obstetrics & Gynecology noted, “prelicensure data on influenza vaccine safety and effectiveness during pregnancy is virtually nonexistent because of strict research guidelines that govern the participation of pregnant women”.
This raises an obvious question: If it is considered unethical to include pregnant women in clinical vaccine safety trials, how is it not also unethical to recommend that all pregnant women be vaccinated in the absence of clinical trials demonstrating that this is safe?
How does this not treat pregnant women as the subjects of a mass uncontrolled experiment without their informed consent?
The Inadequacy of Post-Licensure Safety Studies and Surveillance
Once vaccines get to market, they undergo additional study. However, a CDC recommendation renders vaccination “standard of care” and so randomized, placebo-controlled studies generally are not conducted on the grounds that it would be “unethical” to do so since it would deny the placebo control group the supposed benefits of the presumably safe vaccine. This, of course, is the logical fallacy of begging the question (presuming the proposition to be proven in the premise).
Consequently, most of the studies that the CDC cites to support its policy recommendations are retrospective observational studies. These types of studies are not as well able to control for all the innumerable variables that one must consider, and so, while they may be useful for determining whether an association exists between a vaccine and a given adverse event, they can neither prove nor disprove causality.
To illustrate, all of the studies the CDC cites to support its claim that “Vaccines Do Not Cause Autism” are observational studies. Ironically, one of the studies it cites is a 2004 review by the Institute of Medicine (IOM), which acknowledged that the hypothesis that vaccines administered according to the CDC’s schedule can contribute to the development of autism in children with a genetic or environmental susceptibility cannot be excluded by such studies. Furthermore, none of the studies cited by the CDC and reviewed by the IOM were actually designed to test that hypothesis, which, the IOM further conceded, could explain why they had failed to find an association!
Apart from the lack of proper safety studies for individual vaccines, there has never been a long-term, randomized, placebo-controlled study comparing health outcomes—including rates of allergies, asthma, autoimmune disease, neurodevelopmental disorders, and cancer—between children vaccinated according to the CDC’s routine childhood schedule and children who’ve remained completely unvaccinated. The CDC refuses to do this type of study.
Under the 1986 law granting legal immunity to vaccine manufacturers, due to the insistence of organized parents whose children had been injured by vaccines, a surveillance system was also established called the Vaccine Adverse Event Reporting System (VAERS). But this passive surveillance system is inadequate and not a reasonable substitute for properly designed safety studies, which vaccine manufacturers have little incentive to conduct, especially in light of their legal immunity against damages. One major problem with VAERS is the known underreporting of adverse events.
Both the Congress and the Department of Health and Human Services (HHS), under whose auspices the CDC operates and which also administers the Vaccine Injury Compensation Program, have acknowledged that reports to VAERS represent only a small fraction of actual adverse events. A study by the Agency for Healthcare Research and Quality (AHRQ), which also operates under HHS, found that adverse events from vaccines “are common, but underreported”, representing “fewer than 1% of vaccine adverse events”. The agency proposed a method to automate adverse event reporting rather than relying on passive reporting, but the project reached a dead end when the CDC refused to cooperate on its further development and implementation.
Population Level Effects of Mass Vaccination
Apart from the question of effectiveness in preventing the target disease and the risk of adverse events, there are numerous other factors that simply are not taken into consideration by those who are claiming to know what is best for us and exercising power over us to compel us to behave as they want us to. For example, in addition to individual effects, there are population effects. The same as irresponsible overuse of antibiotics has given rise to antibiotic-resistant “superbugs”, mass vaccination potentially can cause the evolution of viruses and bacteria into even more virulent strains. This is not merely hypothetical, but has been demonstrated in chickens mass vaccinated against Marek’s disease virus. Mass vaccination can also shift the risk burden for disease away from one subpopulation and onto another.
Among human vaccines, the pertussis vaccine provides a useful example. One fact the public is not being told is that, although the public is routinely told that they must vaccinate against pertussis to provide “herd immunity” to infants too young to be vaccinated, public health officials know perfectly well that the theory of vaccine-conferred herd immunity has been falsified. The FDA itself has shown in a study that the vaccine fails to prevent transmission, so that asymptomatic vaccinated individuals can still carry and spread the bacteria to others (and are more likely to be unaware that they are doing so and therefore less likely to quarantine themselves from other household members to protect the baby).
Additionally, the vaccine-conferred immunity is of very short duration, lasting only two to four years, resulting of a shift in the risk burden away from younger children and onto adolescents (so that, again, older vaccinated siblings pose a risk to infants in the household).
Another fact not being communicated to the public is that, due to mass vaccination, the pertussis bacteria, which causes whooping cough, has undergone a genetic shift so that today the dominant circulating strains are deficient in a protein called pertactin (PRN), which is an antigen component of the vaccine. This has contributed to the ineffectiveness of the vaccine, and in the words of the CDC based the findings of a study examining epidemics in Washington and Vermont, “vaccinated patients had significantly higher odds than unvaccinated patients of being infected with PRN-deficient strains.”
Another example of a population level effect of mass vaccination, already touched upon, is how it can shift the risk burden of the disease. For example, the measles vaccine has shifted the burden away from children, in whom it was generally a benign infection (in the US population), and onto those in whom it poses a significantly higher risk of potentially deadly complications: infants and adults. This is because vaccine-conferred immunity is inferior to natural immunity and not as long lasting, and, ironically, because vaccination has interrupted transmission so successfully. In the pre-vaccine era, the circulation of the virus provided a natural boosting effect to those who’d already had it as a child, thus protecting adults generally for a lifetime. Today, though, as vaccine immunity wanes, adults become vulnerable in the event of exposure. Infants are more vulnerable because mothers today are less well able to confer maternal passive immunity, antibodies transferred prenatally through the placenta and postnatally through breastmilk.
Evidence likewise indicates that vaccination against the varicella virus, which causes both chicken pox and shingles, has similarly caused a shift of the risk burden away from children, in whom is generally a mild illness, and onto adolescents and adults, for whom infection poses a greater risk. Due to the loss of natural immunologic boosting from repeated exposures, elderly people who had chicken pox as kids are at greater risk of the dormant virus reactivating and causing shingles. Rather than reconsidering its existing policy, however, the CDC’s answer was to just recommend, starting in 2008, that the elderly also get a newly developed shingles vaccine, too (this has since expanded to include younger adults, as well). A vaccine created to solve the problem created by another vaccine (similar to the practice of prescribing another drug to treat the symptoms caused by a drug previously prescribed to treat symptoms rather than to do anything to actually address the underlying cause).
In a study published in the prestigious journal Vaccine in 2013, a former CDC researcher and his coauthor, looking at CDC data, estimated that the CDC’s policy has not been cost effective, but has rather increased net health care costs. As they commented, vaccine-conferred immunity is “less effective than the natural immunity that existed in communities prior to licensure of the varicella vaccine. Hence, rather than eliminating varicella in children as promised, routine vaccination against varicella has proven extremely costly and has created continual cycles of treatment and disease.”
Other “Non-Specific Effects” of Vaccines
There is a term in the scientific literature used to describe the unintended consequences of vaccination, whether beneficial or detrimental: “non-specific effects”. One non-specific effect that has been found for the diphtheria, tetanus, and whole-cell pertussis (DTP) vaccine is an increased rate of childhood mortality.
The CDC used to recommend this vaccine for the US childhood population, but due to concerns about its safety, it was phased out in favor of a vaccine with an acellular pertussis component (DTaP). The DTP vaccine is still used around the world in developing countries, however, such as in World Health Organization (WHO) campaigns in Africa. There, researchers have found that the vaccine, despite being effective at reducing incidence of the target diseases, is associated with an increased mortality rate.
The hypothesized explanations for this again have to do with the differences between naturally acquired and vaccine-conferred immunity. Inactivated vaccines like DTP tend to bias the immune system toward humoral, or antibody, immunity at the expense of lost cell-mediated immunity, thus causing immune dysfunction that can increase the risk from other diseases that the vaccine is not designed to protect against. As the authors of a study published in the journal EBioMedicine in 2017 remarked, “All currently available evidence suggests that DTP vaccine may kill more children from other causes than it saves from diphtheria, tetanus or pertussis. Though a vaccine protects children against the target disease it may simultaneously increase susceptibility to unrelated infection.”
The influenza vaccine offers another good example of a non-specific effect, which is that getting an annual flu shot can actually increase your risk of getting the flu. While the vaccine is designed to protect against three or four viral strains by stimulating an antibody response, natural influenza infection confers not only humoral, but also a robust cell-mediated immunity. Unlike the vaccine, natural immunity offers cross-protection against not only the infecting strain, but other influenza strains as well, and evidently even against other viruses.
The Assault on Our Right to Informed Consent
The right to informed consent is one of the most fundamental ethics in medicine. In the wake of World War II and revelations about the Nazis’ use of humans for medical experimentation, the international community formally recognized informed consent as a fundamental human right. The Nuremberg Codeestablished medical ethics principles starting with this: “The voluntary consent of the human subject is absolutely essential.”
This means, among other things, that the subject must be in a position “to be able to exercise free power of choice, without the intervention of any element of force, fraud, deceit, duress, overreaching, or other ulterior form of constraint or coercion”.
Additionally, the subject “should have sufficient knowledge and comprehension of the elements of the subject matter involved as to enable him to make an understanding and enlightened decision.”
The right to informed consent has also been codified in the 1966 United Nations International Covenant on Civil and Political Rights, which states under Article 7 that “no one shall be subjected without his free consent to medical or scientific experimentation.”
The updated 2002 edition of the International Ethical Guidelines for Biomedical Research Involving Human Subjects—guidelines promulgated by the World Health Organization (WHO) and the Council for International Organizations of Medical Sciences—states that, “For all biomedical research involving humans the investigator must obtain the voluntary informed consent of the prospective subject or, in the case of an individual who is not capable of giving informed consent, the permission of a legally authorized representative….”
This right is also codified in the Universal Declaration on Bioethics and Human Rights, adopted at the United Nations Educational, Scientific and Cultural Organization (UNESCO) in October 2005: “Any preventive, diagnostic and therapeutic medical intervention is only to be carried out with the prior, free and informed consent of the person concerned, based on adequate information…. Scientific research should only be carried out with the prior, free, express and informed consent of the person concerned. The information should be adequate, provided in a comprehensible form and should include modalities for withdrawal of consent…. In no case should a collective community agreement or the consent of a community leader or other authority substitute for an individual’s informed consent.” (Emphasis added.)
Yet substituting individual informed consent with state authority is precisely what the federal and state governments are doing when it comes to the practice of vaccination. When the state uses coercion to gain compliance, it constitutes an assault on this fundamental human right. Furthermore, neither medical professionals nor the major media are doing their duty by providing people with the knowledge they need to be able to make an informed choice, but instead are regurgitatingdeceitful vaccine propaganda to persuade or intimidate them into behaving as government bureaucrats would have them do.
The population is being bullied into compliance with dangerously shortsighted government diktats. Power hungry bureaucrats and technocrats treat vaccination as a one-size-fits-all solution despite great variability in individual risk both from the diseases the vaccines are designed to prevent and from the vaccines. They have no respect for individual rights or the doctor-patient relationship. California Senator Richard Pan, for example, considers doctors writing medical exemptions to state vaccine mandates as doing something that is “not the practice of medicine but of a state authority to licensed physicians”. Essentially, from his authoritarian perspective, “physicians are fulfilling an administrative role”. There is no room for informed consent. Doctors are not free to practice as they deem best for their patients, and informed consent for their patients is not an option.
But bureaucrats in Washington or state capitals simply do not have the knowledge required to be able to make that determination for other individuals. When it comes to our children, only the parents and their family doctor have the specialized knowledge of the child that is necessary to be able to do the individual risk-benefit analysis that required for informed consent.
Many who do choose willingly to comply with public policy do so because they unquestioningly believe the dogma they are told, that “vaccines are safe and effective”, and who therefore remain incapable of such a risk-benefit analysis. Not all vaccines are safe. Not all are effective. The risks and benefits are not the same for everyone. And the long-term unintended consequences need also to be considered.
Many others who are aware enough to question public policy still comply because there will be state retribution if they don’t. Informed consent is not happening. Consequently, public vaccine policy effectively treats the entire population as the subjects of a mass uncontrolled experiment with most people remaining unaware that they are being experimented upon by blind authoritarians trying to play God by controlling us.
It’s time for that to stop—and for mainstream journalists to start doing their jobs and reporting seriously on this critically important issue. The lives, health, and liberty of entire future generations of humanity are depending on it.
The first eight months of WWII with no fighting – was called The Phoney War. Using millimetre waves as a fifth-generation or 5G wireless communications technology is a phoney war of another kind.
This phoney war is also silent, but this time shots are being fired – in the form of laser-like beams of electromagnetic radiation(EMR) from banks of thousands of tiny antennas[1] – and almost no one in the firing line knows that they are being silently, seriously and irreparably injured.
In the first instance, 5G is likely to make people electro-hypersensitive (EHS).[2] Perhaps it was sitting in front of two big computer screens for many of the 18 years I worked at the UN that made me EHS. When the UN Office at Vienna installed powerful WiFi and cellphone access points – designed to serve large, public areas – in narrow, metal-walled corridors throughout the Vienna International Centre in December 2015, I was ill continuously for seven months.
I did my best for two and a half years to alert the UN staff union, administration and medical service to the danger to the health of UN staff of EMR from these access points, but was ignored. That’s why, in May 2018, I took the issue to the UN Secretary-General, António Guterres [transcript]. He is a physicist and electrical engineer and lectured on telecommunications signals early in his career, yet asserted that he knew nothing about this. He undertook to ask the World Health Organization to look into it, but seven months later those public access points remain in place. I received no replies to my many follow-up emails.
As a result, I welcomed the opportunity to join the effort to publish an International Appeal to Stop 5G on Earth and in Space because it was clear to me that, despite there having been 43 earlier scientific appeals, very few people understood the dangers of EMR. My experience as an editor could help ensure that a new 5G appeal, including the issue of beaming 5G from space, was clear, comprehensive, explanatory, and accessible to the non-scientist. The International Appeal to Stop 5G on Earth and in Space is fully referenced, citing over a hundred scientific papers among the tens of thousands on the biological effects of EMR published over the last 80 years.[3]
Having spent years editing UN documents dealing with space, I know that outer space is hotly contested geopolitically and any untoward event involving a military satellite risks triggering a catastrophic response.[4] Space law is so inadequate – just one example is the complexity of space liability law [5],[6] – that we could really call the Earth orbits a new Wild West. China caused international consternation in 2007 when it demonstrated an anti-satellite weapon by destroying its own satellite. Space debris is the main concern among space-faring nations, with a so-called Kessler syndrome positing a cascade of space debris that could make the Earth orbits unusable for a thousand years.[7] Does launching 20,000+ commercial 5G satellites in such circumstances sound rational to you?
I live in Vienna, Austria, where the 5G rollout is suddenly upon us. Within the last five weeks, pre-5G has been officially announced at Vienna airport and 5G at the Rathausplatz, the main square in Vienna, which attracts tens of thousands of visitors to its Christmas market each December and skating rink each January, which are special treats for children. Along with birds and insects, children are the most vulnerable to 5G depredation because of their little bodies.[8]
Friends and acquaintances and their children in Vienna are already reporting the classic symptoms of EMR poisoning:[9] nosebleeds, headaches, eye pains, chest pains, nausea, fatigue, vomiting, tinnitus, dizziness, flu-like symptoms, and cardiac pain. They also report a tight band around the head; pressure on the top of the head; short, stabbing pains around the body; and buzzing internal organs. Other biological effects such as tumours and dementia usually take longer to manifest, but in the case of 5G, which has never been tested for health or safety, who knows?[10]
Seemingly overnight a forest of 5G infrastructure has sprouted in Austria. In the space of three weeks one friend has gone from robust health to fleeing this country, where she has lived for 30 years. Each person experiences EMR differently. For her, it was extreme torture so she and I spent her last two nights in Austria sleeping in the woods. Interestingly, as she drove across southern Germany, she suffered torture even worse than in Austria, while in northern Germany she had no symptoms at all and felt completely normal, which suggests that there has been as yet no 5G rollout there.
There are no legal limits on exposure to EMR. Conveniently for the telecommunications industry, there are only non-legally enforceable guidelines such as those produced by the grandly named International Commission on Non-Ionising Radiation Protection, which turns out to be like the Wizard of Oz, just a tiny little NGO in Germany that appoints its own members, none of whom is a medical doctor or environmental expert.[11]
Like the Wizard of Oz, ICNIRP seems to have magical powers. Its prestidigitation makes non-thermal (non-heating) effects of EMR exposure disappear into thin air, for taking into account the tens of thousands of research studies demonstrating the biological effects of EMR would invalidate its so-called safety guidelines.[12]It has bewitched the International Telecommunication Union, part of the UN family, into recognising these guidelines.[13] And one little email sent to ICNIRP in October 2018 to submit Professor Martin Pall’s comments on ICNIRP’s new draft guidelines conjured up an immediate explosion of interest in the sender’s online presence – which had hitherto attracted none – from companies and individuals worldwide, one country’s immigration authorities, the office of the Austrian Chancellor (head of government), a firm of lawyers in Vienna and even Interpol![14],[15]
I hope that people read and share our Stop 5G Space Appeal to wake up themselves and others quickly and use it to take action themselves to stop 5G. Even eight short months of this 5G Phoney War could spell catastrophe for all life on Earth. Elon Musk is set to launch the first 4,425 5G satellites in June 2019 and “blanket” the Earth with 5G, in breach of countless international treaties. This could initiate the last great extinction, courtesy of the multi-trillion-US-dollar 5G, the biggest biological experiment and most heinous manifestation of hubris and greed in human history.[10]
People’s first reaction to the idea that 5G may be an existential threat to all life on Earth is usually disbelief and/or cognitive dissonance. Once they examine the facts, however, their second reaction is often terror.
We need to transcend this in order to see 5G as an opportunity to empower ourselves, take responsibility and take action. We may have already lost 80 per cent of our insects to EMR in the last 20 years.[16] Our trees risk being cut down by the millions in order to ensure continuous 5G signalling for self-driving cars, buses and trains.[17] Are we going to stand by and see ourselves and our children irradiated, our food systems decimated, our natural surroundings destroyed?
Our newspapers are now casually popularising the meme that human extinction would be a good thing,[18],[19] but when the question becomes not rhetorical but real, when it’s your life, your child, your community, your environment that is under immediate threat, can you really subscribe to such a suggestion? If you don’t, please sign theStop 5G Appeal and get active in contacting everyone you can think of who has the power to stop 5G, especially Elon Musk[20] and the CEOs of all the other companies planning to launch 5G satellites, starting in just 20 weeks from now. Life on Earth needs your help now.
The transcript of my exchange with the UN Secretary-General of 14 May 2018 follows:
Staff member:Mr. Secretary-General
UN staff have repeatedly been told that they are the most important resource of this Organization.
Since December 2015, the staff here at the Vienna International Centre have been exposed to off-the-scale electromagnetic radiation from WiFi and mobile phone boosters installed on very low ceilings throughout the buildings. Current public exposure levels are at least one quintillion times (that’s 18 zeros) above natural background radiation according to Professor Olle Johansson of the Karolinska Institute in Sweden.
The highly dangerous biological effects of EMFs have been documented by thousands of studies since 1932 indicating that we may be facing a global health catastrophe orders of magnitude worse than those caused by tobacco and asbestos.
Mr. Secretary-General, on the basis of the Precautionary Principle, I urge you to have these EMF-emitting devices removed immediately and to call a halt to any rollout of 5G at UN duty stations, because it is designed to deliver concentrated and focused electromagnetic radiation in excess of 100 times current levels in the same way as do directed energy weapons.
In line with the UN Guiding Principles on Business and Human Rights, to “Protect, Respect and Remedy”, 5G technologies MUST be subjected to an independent health and safety assessment before they are launched anywhere in the world.
There is currently an international appeal (https://www.emfscientist.org/index. php/emf-scientist-appeal) signed by 237 EMF scientists from 41 nations urging the UN and particularly the WHO to exert strong leadership in fostering the development of more protective EMF guidelines, encouraging precautionary measures, and educating the public about health risks, particularly risk to children and fetal development.
Mr. Secretary-General, we have a unique opportunity here at the UN Office at Vienna. Since our medical records are digitised, you have the possibility of releasing data on a closed population exposed to off-the-scale levels of electromagnetic radiation to establish if there have already been abnormal health consequences for the UN staff here in the last 28 months.
I urge you to do so and stop any 5G rollout in these buildings immediately.
Thank you.
UN Secretary-General:Sorry, because you are talking to someone who is a little bit ignorant on these things. You’re talking about the WiFi systems?
Staff member:On the ceilings of these buildings, WiFi boosters and cell phone boosters were installed without consultation, without information to staff in December 2015. Now, if you understand electromagnetic radiation, the signal is – if you cannot get a signal from your mobile phone, the signal goes to maximum strength and that then bounces off metal walls affecting the body multiple times at maximum exposure levels. So the situation here is extremely dangerous. I have heard anecdotally of many people who have had health problems. I don’t know if they are related but the Precautionary Principle would dictate that we use our medical records to look into this and that we remove these dangerous devices immediately. Thank you.
UN Secretary-General:Well, I’m worried because I put those devices in my house.[Laughter & applause]
Staff member:Not a good idea!
UN Secretary-General: This I will have to – I confess my ignorance on this but I’m going to raise this with WHO [World Health Organization] – which I think is the organisation that might be able to deal with it properly for them to put someone – their staff or organisations to work on that because I must confess I was not aware of that danger – [humorously] to the extent that I put those things in the rooms of my house – in the ceiling.
Staff member:I would suggest that everybody start looking into this issue and particularly into 5G, which 237 scientists from 41 countries consider a threat that is far worse than the tobacco and asbestos threats of the past.
UN Secretary-General:Well, maybe I have learned something completely new. I hope it will be very useful to me but I confess it is the first time I hear about it.
*
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Claire Edwards, BA Hons, MA – worked for the United Nations as Editor and Trainer in Intercultural Writing from 1999 to 2017.
Notes
[1] Delos, Peter. “The Way to a New Phased Array Radar Architecture.” TechTime: Electronics & Technology News. January 15, 2018. Accessed January 1, 2019. https://techtime.news/2018/01/ 15/analog-devices-phased-array-radar/. “Although there is a lot of discussion of massive MIMO and automotive radar, it should not be forgotten that most of the recent radar development and beamforming R&D has been in the defense industry, and it is now being adapted for commercial applications. While phased array and beamforming moved from R&D efforts to reality in the 2000s, a new wave of defense focused arrays are now expected, enabled by industrial technology offering solutions that were previously cost prohibitive.”
[2] “Electrosensitive Testimonials.” We Are The Evidence. 2018. Accessed January 1, 2019.http://wearetheevidence.org/adults-who-developed-electro-sensitivity/. “WATE intends to expose the suppressed epidemic of sickness, suffering and human rights crisis created by wireless technology radiation; elevate the voice of those injured; defend and secure their rights and compel society and governments to take corrective actions and inform the public of the harm.”
[3] Glaser, Lt. Z. “Cumulated Index to the Bibliography of Reported Biological Phenomena (‘effects’) and Clinical Manifestations Attributed to Microwave and Radio-frequency Radiation: Report, Supplements (no. 1-9).” BEMS Newsletter B-1 through B-464 (1984). Accessed January 1, 2019. http://www.cellphonetaskforce.org/wp-content/uploads/2018/06/Zory-Glasers-index.pdf. Lt. Zorach Glaser, PhD, catalogued 5,083 studies, books and conference reports for the US Navy through 1981.
“However, as more countries integrate space into their national military capabilities and rely on space-based information for national security, there is an increased chance that any interference (either actual or perceived) with satellites could spark or escalate tensions and conflict in space or on Earth. This is made all the more difficult by the challenge of determining the exact cause of a satellite malfunction: whether it was due to a space weather event, impact by space debris, unintentional interference, or deliberate act of aggression.”
[5] “Space Law: Liability for Space Debris.” Panish, Shea & Boyle LLP. 2018. Accessed January 1, 2019.https://www.aviationdisasterlaw.com/liability-for-space-debris/. “Filing a lawsuit against SpaceX for space debris is a little different than one against the commercial industry or state-sponsored launch. Since SpaceX is a private company, injured parties can file claims directly against the establishment in accord with the state’s personal injury laws. For the claim to be successful, the plaintiff will have to prove that SpaceX was negligent in some way that caused the space debris collision. Space law is notoriously complex, making it very difficult for injured parties to recover for [sic] their damages in California.”
[7]Kessler, D. J., P. M. Landry, B. G. Cour-Palais, and R. E. Taylor. “Aerospace: Collision Avoidance in Space: Proliferating Payloads and Space Debris Prompt Action to Prevent Accidents.” IEEE Spectrum 17, no. 6 (1980): 37-41.
[8] Morgan, L. Lloyd, Santosh Kesari, and Devra Lee Davis. “Why Children Absorb More Microwave Radiation than Adults: The Consequences.” Journal of Microscopy and Ultrastructure 2, no. 4 (December 2014): 197-204. Accessed January 1, 2019. https://www.sciencedirect.com/ science/article/pii/S2213879X14000583. Highlights: (1) Children absorb more microwave radiation (MWR) than adults. (2) MWR is a Class 2B (possible) carcinogen. (3) The fetus is in greater danger than children from exposure to MWR. (4) The legal exposure limits have remained unchanged for decades. (5) Cellphone manuals warnings and the 20 cm rule for tablets/laptops violate the “normal operating position” regulation.
[10]FCC Chairman on 5G: “We won’t study it, regulate it, have standards for it.” Youtube. June 20, 2016. Accessed January 1, 2019. www.youtube.com/watch?v=Bwgwe01SIMc. Notes in video: Ultra-high frequency radiation (24 to 100 GHz or more); aimed and amplified signals; massive deployment of towers; worth billions; no standards, no testing; sharing with satellite and military operations; all areas (including rural areas) to be saturated with radiation; all local deployments to be fast-tracked; everything to be microchipped.
[11] Dariusz Leszczynski, PhD. “Is ICNIRP Reliable Enough to Dictate Meaning of Science to the Governmental Risk Regulators?” Between a Rock and a Hard Place(blog), April 8, 2018. Accessed January 2, 2019.https://betweenrockandhardplace.wordpress.com/type/gallery/. “The major problems of ICNIRP are: (1) it is a “private club” where members elect new members without need to justify selection; (2) lack of accountability before anyone; (3) lack of transparency of their activities; (4) complete lack of supervision of its activities; (5) skewed science evaluation because of the close similarity of the opinions of all members of the Main Commission and all of the other scientists selected as advisors to the Main Commission.”
[13] ITU Telecommunication Development Sector Study Group 2: Session on Modern Policies, Guidelines, Regulations and Assessments of Human Exposure to RF-EMF. Session 1: Recent Activities on Human Exposure to RF-EMF in ITU and ICNIRP, Geneva, Switzerland. October 10, 2018. Accessed January 2, 2019.www.itu.int/en/ITU-D/Study-Groups/2018-2021/Pages/ meetings/session-Q7-2-oct18.aspx. “Session 1 will discuss some of the recent activities held in ITU and describe the latest updates to the ICNIRP (International Commission on Non‐Ionizing Radiation Protection) guidelines.”
[15] Cooperation Agreement Between The International Criminal Police Organization Interpol and The International Telecommunication Union. Plenipotentiary Conference (PP-18) Dubai 29 October–16 November 2018. Accessed January 2, 2019. https://www.itu.int/dms_pub/itu-s/md/18/pp/c/S18-PP-C-0047!!MSW-E.docx. “2. In implementing the Agreement, each Party shall act within their respective areas of competence. More specifically, the implementation of the Agreement by ITU shall not exceed beyond its mandate pertaining to building confidence and security in the use of ICTs, in accordance to Plenipotentiary Conference Resolution 130 (Rev. Busan, 2014) and to its role on child online protection in accordance to Plenipotentiary Conference Resolution 179 (Rev. Busan, 2014), whereas the implementation of the Agreement by INTERPOL shall not exceed its mandate as defined by article 2 of its Constitution which include activities pertaining to cybercrime and online child exploitation”. (emphasis added)
[20] “Planet Earth: Worldwide 5G Radiation from Orbit?” Letter from Claus Scheingraber, Roland Wolff and others to Elon Musk. June 18, 2018. Brunnthal, Germany. “… We are sure that your satellite project is already at an advanced stage. But even if much money has been invested, one should consider that it is only a matter of time until the fact of damaging health potential of mobile communications – and especially of 5G-mobile communication – can no longer we overlooked. Therefore we emphatically recommend not to implement the satellite project.” (Letter in German) (Letter in English)
