Michael Bryant
21st Century Wire
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In the conventional narrative it is accepted as an article of faith that vaccines are miraculous discoveries responsible for global disease eradication and are the most important medical product for disease prevention.
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It is widely believed that if we stopped, or even reduced vaccinations, we would be going back to the dark ages. Any individual that challenges this vaccine orthodoxy is seen as a heretic.
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The United States Childhood Immunization Schedule – An Overview
In the past few decades the childhood vaccine schedule in the United States has exploded into what is now the most aggressive childhood vaccination schedule in the world. It wasn’t always this way. Most baby boomers likely had only 2 or 3 vaccinations- polio, smallpox and DTP with never more than one shot given per visit.
With the recent addition of the COVID-19 vaccines to the childhood schedule the number of recommended injections ballooned to a regimen of 72 injections of 90 antigens by age eighteen for any child that undergoes the full immunization schedule circa 2023.
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The first vaccine mandate in the United States was enacted in Massachusetts in 1810 and was centered on smallpox. The legislation was essentially an ad hoc law which gave local health boards the authority to require vaccination.
The first public school mandate was issued in Massachusett in the 1850’s. At that time the only vaccine of interest was for smallpox. By the end of the 1800s most states in New England had smallpox vaccine requirements for children attending public schools.
The next significant stride in vaccine recommendations and requirements for children would arrive a century later in 1954, focusing on the polio vaccine developed by Jonas Salk.
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The 1960s and 1970s saw a wave of new vaccines hit the market. A second type of polio vaccine was developed along with the first Hepatitis B vaccine. Measles vaccines were developed as a single vaccine and then combined with the mumps and rubella vaccines to create the “MMR” vaccine.
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By 1977, the U.S. federal government had set up the Childhood Immunization Initiative which sought to increase vaccination rates in children against seven diseases (diphtheria, measles, mumps, pertussis, poliomyelitis, rubella, tetanus) for which vaccines had been developed. This began the process by which all 50 states would adopt mandatory school vaccinations.
In the 1980s, vaccines against Hepatitis B, Haemophilus influenzae type b, and pneumococcal disease were recommended for children at different ages. By 1983 the number of recommended injections had increased to 23 doses of 7 vaccines by age six.
In 1986, the National Childhood Vaccine Injury Act created a system of passive and active surveillance for cases of adverse reactions to vaccines as well as a mechanism to compensate any persons injured by vaccines.
With the passage of the 1986 Act and its implementation in 1988, a liability shield for pharmaceutical companies was created. On the heels of the 1986 Act the number of vaccines placed on the CDC schedule would escalate.
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This dizzying array of injections in the childhood immunization schedule begins on a child’s first day of life with the Hepatitis B vaccine.
Hepatitis B – The Disease: A Case Study In Manufacturing Public Perception
The first question every parent should ask when considering the Hepatitis B vaccine is, “Does my child need a vaccine for Hepatitis B on the first day of life?”
Given the low risk of newborns acquiring the HepB infection and the ease with which pregnant mothers can be screened it’s fair to ask why a newborn would need the HepB vaccine?
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The risk groups listed are, “injection drug users, homosexual men, sexually active heterosexuals, infant/children of immigrants from disease-endemic areas, sexual/household contacts of infected persons, infants born to infected mothers, health care workers and hemodialysis patients.”
What was it that changed the CDC’s earlier 1982 recommendation, which targeted only a small “at-risk” population, into a set of more aggressive policies that would result in the 1991 recommendation that all infants get three doses of HBV by 18 months of age?
And how did the HepB vaccine become compulsory for all schoolchildren in 47 states by the year 2000 even as the CDC admits that they lack proof of HepB being transmitted in a school setting?
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In 2017 the Informed Consent Action Network (ICAN) received a tip from a supporter that the clinical trials used by the FDA to license the two children’s HepB vaccines, Engerix-B and Recombivax HB, only reviewed safety data for a few days after injection.
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Dangers of the HepB Vaccine- An Open Secret
In the first months of life a child’s brain and biological systems are at critical stages of development.
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To the extent that Hepatitis B is a danger to anyone, that risk is understood to be through sexual contact or sharing needles. A sexually transmitted risk or a needle exchange risk means there is little to no chance of Hepatitis B infection for infants calling into question the fundamental rationale for this vaccine.
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In a 2013 study, Aluminum in the Central Nervous System: Toxicity in Humans and Animals, Vaccine Adjuvants, and Autoimmunity, Shaw and Tomljenovic concluded, “In young children, a highly significant correlation exists between the number of pediatric aluminum-adjuvanted vaccines administered and the rate of autism spectrum disorders. Many of the features of aluminum-induced neurotoxicity may arise, in part, from autoimmune reactions, as part of the autoimmune/inflammatory induced by adjuvants (ASIA) syndrome.”
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Cui Bono?
According to statistics, Hepatitis B causes death in fewer than one quarter of one percent of those infected. It is a near certainty that even that rate is an overestimate since deaths of hepatitis B infected drug addicts and alcoholics is more likely due to their habits which destroy their liver and other vital organs and not the disease.
In 1986, five years before the CDC began pushing for vaccination of all newborns, the US had documented fewer than 280 cases of hepatitis B infection in children under age 14. Newborns are probably the least likely human beings on the planet at risk of actually getting hepatitis B.
Given that most infants are not at risk for Hepatitis B in the United States and given the copious documentation linking the Hepatitis B vaccine to various pathologies (here, here and here) we return to the question: Why the fanatical push for universal HepB vaccination for children?
If we look at the HepB childhood vaccination program from a perspective of health and “saving lives” we are confronted with a world of contradictions and manipulations- none of it makes sense.
If looked at it through the lens of power, money and control everything makes perfect sense.
A 2005 letter written by Dr. Marc Girard to the Director General of the World Health Organization referenced a correspondence he had with an Indian colleague, Dr J. Puliyel, on the false data being disseminated by the WHO about the epidemiology of hepatitis B in India.
This exchange gives us insight into the processes by which a once non-existent threat is turned into a public health crisis and the motives behind this.
Girard noted that, “the mechanisms of the deception described by Dr Puliyel were exactly comparable to those I observed in my own country — and of course with the same results: a plea of “experts” to include hepatitis B vaccination in the national vaccination program, in spite of its costs and, its unprecedented toxicity.” [Emphasis added]
Dr. Girard went on to state: “It is blatant that in the promotion of the hepatitis B vaccination, the WHO has never been more than a screen for an undue commercial promotion, in particular via the Viral Hepatitis Prevention Board (VHPB), created, sponsored and infiltrated by the manufacturers.
In Sept 1998, while the dreadful hazards of the campaign had been given media coverage in France, the VHPB met a panel of “experts”, the reassuring conclusions of which were extensively announced as reflecting the WHO’s position: yet some of the participants in this panel had no more “expertise” than that of being employees of the manufacturers.” [Emphasis added]
Girard also drew attention to a 1997 interview published in the French journal Sciences et Avenir in which GlaxoSmith Beecham’s business manager admitted, “We started increasing the awareness of the European Experts of the World Health Organization (WHO) about Hepatitis B in 1988. From then to 1991, we financed epidemiological studies on the subject to create a scientific consensus about hepatitis being a major public health problem. We were successful because in 1991, WHO published new recommendations about hepatitis B vaccination.”
This cynical admission by one of the primary manufacturers of the Hepatitis B vaccine offers a glimpse into how the time honored strategy of problem-reaction-solution is applied in the Pharmaceutical Industry
The disease itself is seen as superfluous, all that is necessary is to create the perception that there is a widespread public health crisis which requires a heroic and international medical intervention in the form of a vaccine which, curiously, was already in production leading into the “crisis.”
Such a frank admission reinforces the facts surrounding the history of Hepatitis B, there was little to no problem with this disease until after the vaccine became available and for marketing reasons they had to change the image of the disease.
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A Final Word
In two separate hearings in 1999 Michael Belkin, whose daughter died of Sudden Infant Death Syndrome (SIDS) immediately after receiving a Hepatits B vaccine dosage, called the HepB vaccine policy a ”bureaucratic vaccination program that is on auto-pilot flying into a mountain” and accused CDC bureaucrats of “hav[ing] a vested interest in the status quo.”
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They also cause significant illness and disability, eg severe allergies, automimmune disease and susceptibility to cancer.
I would add the rest of the childhood vaccines to that list, as none of them have been safety tested.
As director of the National Agency for Infectious Disease and Allergy, Fauci systematically blocked safety trials of childhood vaccines, supposedly because it was unfair to children in the control group.