Merck’s Julie Gerberding Wins Industry “Woman Of The Year” Award For Putting Profits Ahead Of Human Health

By Richard Enos

In Brief

  • The Facts: Julie Gerberding, the Healthcare Businesswomen’s Association ‘Woman of the Year,’ is a prime example of someone who has gone through the revolving door between government regulatory agencies and the corporations they are supposed to be regulating.
  • Reflect On: It is becoming clear that our authorities in government and business alike are making decisions purely for their own interests, in utter disregard for human safety and well-being. How does this realization play a role in our awakening?

If you are not already clear about how the Corporatocracy that we live in is able to consistently serve their own power and wealth interests at the expense of our heath, well-being and prosperity, then the case of Julie Gerberding should provide some excellent insight. Her career path makes her the poster child for people who want to succeed in the world by embracing the corrupt, deceitful system that is currently in place.

Here is the blueprint: first, become an expert in a very specific area through a good old fashioned Western education. Use the talent and intelligence you have been blessed with to move up the ranks in your chosen industry to gain a position of power within the highest government agency in your field. Work in close collaboration with the corporations you are supposed to be the watchdogs for, and display a particular talent to get away with murder, not only deflecting obvious conflicts of interest and preventing them from materializing into lawsuits, but also demonstrating a highly developed ability–and willingness–to garner public trust around the safety and effectiveness of the products being pushed by the corporations you are colluding with.

Julie Gerberding

Julie Gerberding completed her internship and residency in internal medicine at UCSF, where she also served as Chief Medical Resident before completing her fellowship in Clinical Pharmacology and Infectious Diseases. She earned an M.P.H. degree at the University of California, Berkeley in 1990.

Before becoming CDC Director and ATSDR Administrator, Gerberding was Acting Deputy Director of the National Center for Infectious Diseases (NCID). She joined CDC in 1998 as Director of the Division of Healthcare Quality Promotion, NCID, where she developed CDC’s patient safety initiatives and other programs to prevent infections, antimicrobial resistance, and medical errors in healthcare settings.

But it is perhaps her talent in knowing how to speak with quiet authority, and a persona that people felt they could trust, that not only helped her rise up in the ranks of the government’s regulatory bodies, but also made giants of the corporatocracy take notice and treat her as one of their own. Knowing how to appeal to people emotionally, with eloquence and persuasion, is something you cannot force, nor can you teach it. Some people just have that power. What they decide to do with it is another matter.

Less than a year after she resigned from her CDC post in in January 2009, she was hired as president of Merck’s vaccine division. Now we can look at the low-hanging fruit and remark that during her tenure at the CDC, Merck became the manufacturer of 14 of the 17 vaccines ‘recommended’ for children by the CDC, and 9 of the 10 vaccines ‘recommended’ for adults by the CDC. The conflict of interest here is beyond obvious, and one would be reasonable to assume that this appointment, which garnered over $5 million in stock options alone, amounted to payback for favors done to Merck while head of the CDC.

But I believe Merck saw genuine value in the type of leadership Gerberding brought to the table: a cold and calculating devotion to the bottom line, covered over by a veneer of compassion-like-symptoms and a trustworthy tone of authority. In the pharmaceutical industry, these qualities are gold.

CNN Interview

During our bi-weekly broadcast on CETV, Joe Martino and I had a discussion about the ‘revolving door’ between government regulatory agencies and the corporations they serve. We look at statistics that would literally make your head spin about the hordes of people who have enjoyed the freedom to move from working on one side of the aisle to the other. Typically this pattern serves those willing to ‘play ball’ with corporate powers in their capacity as government regulators, to then be rewarded by the wealthy corporations with cushy jobs and board appointments.

In the case of Julie Gerberding, we dove deep into a CNN interview Gerberding did with Sanjay Gupta while she was at the CDC around the time that the Hannah Poling case was making headlines and getting widespread public attention. (Hannah Poling was the first child to receive money from the National Vaccine Injury Compensation Program for her vaccine injury; in essence, the government conceded that vaccines caused Hannah Poling’s autism). Big Pharma seemed to be in need of a reassuring voice directed at the public to prevent a massive exodus of parents from the growing vaccine schedules being lined up for their children.

Joe and I talked about the various techniques Gerberding uses to deftly move the conversation from a very vague ‘admission’ of what the government had conceded to assurances that all caring parents should continue to have their children vaccinated.

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By some accounts, Julie Gerberding had a significant impact at this time in preventing a complete loss in confidence in vaccine safety, which would have been a major disaster for the pharmaceutical industry. Makes you wonder why she didn’t win the Healthcare Businesswomen’s Association ‘Woman of the Year’ award sooner.

The Takeaway

As difficult as it is for some of us to accept, the belief that those in authority have humanity’s best interests at heart has long run its course. It is an important part of our collective evolution that we realize we cannot count on our elected officials, corporate leaders, bureaucrats or other authority figures to make decisions that are in our best interests, because by and large we are seeing that they are only making decisions in their own interests, for the expansion and consolidation of their power. As individuals we must seek to become sovereigns, and as sovereigns to link together and awaken to our collective power to consciously create the type of world we really want to live in.


Richard EnosMy Master’s thesis on “The Anatomy of Self-Overcoming in Nietzsche” was only the beginning of my journey of exploration into consciousness. I have since lived and taught in Korea, studied yoga in India, written a book entitled “Parables for the New Conversation”, built a film and theater production company (pandorasboxoffice.ca), and started a family. While I endeavor to foster positive change in the world through my works, I hold fast to CE’s maxim ‘Change starts within’. I am humbled and grateful to have joined the CE team as of April 2018 as a contributing writer. You can reach me at [email protected]

This article was sourced from Collective Evolution.

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If Truth Be Told: Pregnancy Vaccines Are Not Tested For Carcinogenesis, Mutagenesis, Impairment of Fertility Proof In Vaccine Package Inserts

By Catherine J. Frompovich

Carcinogenesis: capable of causing cancer(s)
Mutagenesis: capable of causing birth defects
Impairment of Fertility: the ability to interfere with reproduction


What in the world are the dingbats at HHS/CDC/FDA and Big Pharma thinking and implementing in mandating pregnant females receive vaccines which have not been tested for the very horrors pregnant mothers—or anyone else—would want to consider IF they knew the truth about those vaccines?

Below are vaccines pregnant females must receive only relatively recently; the information is taken from vaccine package inserts online. Each vaccine has a Section 13 Nonclinical Toxicology wherein the vaccine manufacturer bold-faced tells the FACT that testing for the vaccine’s capability to cause cancer, birth defects and to interfere with human reproduction HAVE NOT BEEN DONE and, apparently, will never be done, so as to be able to make unknowns a given without legal liability!

Is that science-based medicine?

Is that a fraudulent practice by medicine and pharmacology?

Vaccines Required During Pregnancy

  1. Flu (influenza)

FLUARIX QUADRIVALENT.
GKS 13 NONCLINICAL TOXICOLOGY 13.1

Carcinogenesis, Mutagenesis, Impairment of Fertility FLUARIX QUADRIVALENT has not been evaluated for carcinogenic or mutagenic potential or male infertility in animals. Vaccination of female rats with FLUARIX QUADRIVALENT had no effect on fertility [see Use in Specific Populations (8.1)]. — GlaxoSmithKline [Pg. 16]

  1. Tetanus toxoid, reduced diphtheria toxoidand acellular pertussis (Tdap) vaccine

GKS Boostrix tetanus toxoid, reduced diphtheria toxoid and acellular pertussis vaccine, adsorbed

13 NONCLINICAL TOXICOLOGY
13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

BOOSTRIX has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility. GlaxoSmithKline [Pg. 16]

Examples of vaccines to avoid during pregnancy include:

Chickenpox (varicella) vaccine
Measles-mumps-rubella (MMR) vaccine
Shingles (varicella-zoster) vaccine

Source: MayoClinic.org

Merck’s MMR II

Carcinogenesis, Mutagenesis, Impairment of Fertility M-M-R II has not been evaluated for carcinogenic or mutagenic potential, or potential to impair fertility.

Pregnancy Animal reproduction studies have not been conducted with M-M-R II. It is also not known whether M-M-R II can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Therefore, the vaccine should not be administered to pregnant females; furthermore, pregnancy should be avoided for 3 months following vaccination (see IN (see INDICATIONS AND USAGE, Non-Pregnant Adolescent and Adult Females and CONTRAINDICATIONS). — Merck [Pg.6]

Institute for Vaccine Safety
http://www.vaccinesafety.edu/package_inserts.htm
Johns Hopkins Bloomberg School of Public Health
61 vaccine package insert publications
Lists: Vaccine, Antigen(s), Manufacturers, Latest Version [pkg. insert]

Based upon the above information, why aren’t allopathic medical doctors demanding proof of vaccine safety from CDC/FDA and Big Pharma regarding any vaccines ability to cause cancer(s), birth defects and interfere with fertility?

Where is congressional oversight, or is Congress afraid if they investigated, they’d lose their election campaign funding?

If Big Pharma’s largess didn’t fund much of CDC/FDA [The Biopharmaceutical Industry Provides 75% Of The FDA’s Drug Review Budget. Is This A Problem?], and Congress did not receive Big Pharma lobbyists’ election-cycle donations, would U.S. citizens have a better healthcare—or is it sickness care—system

According to Open Secrets, during the 2016 election cycle, the industry gave over$16 million to 399 members of the House of Representatives, an average of more than $40,000 per member. They also gave more than $7 million to a total of 97 senators, at an average of roughly $75,000.

Source: CitizensForEthics.org

If only truth be told!

Catherine J Frompovich (website) is a retired natural nutritionist who earned advanced degrees in Nutrition and Holistic Health Sciences, Certification in Orthomolecular Theory and Practice plus Paralegal Studies. Her work has been published in national and airline magazines since the early 1980s. Catherine authored numerous books on health issues along with co-authoring papers and monographs with physicians, nurses, and holistic healthcare professionals. She has been a consumer healthcare researcher 35 years and counting.

Catherine’s latest book, published October 4, 2013, is Vaccination Voodoo, What YOU Don’t Know About Vaccines, available on Amazon.com.

Her 2012 book A Cancer Answer, Holistic BREAST Cancer Management, A Guide to Effective & Non-Toxic Treatments, is available on Amazon.com and as a Kindle eBook.

Two of Catherine’s more recent books on Amazon.com are Our Chemical Lives And The Hijacking Of Our DNA, A Probe Into What’s Probably Making Us Sick (2009) and Lord, How Can I Make It Through Grieving My Loss, An Inspirational Guide Through the Grieving Process (2008)

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CDC And The Medical Deep State

By Richard Gale and Gary Null PhD

For over two decades, American families have faced an unscrupulous foe that threatens the public health and welfare. It is a rogue, unmanageable institution within our federal government, now seemingly beholden solely to private interests. Citizens have been horribly mistaken in believing that the nation’s leading health agency, the Centers for Disease Control (CDC), honors its mandate to protect the public from “dangerous health threats,” both domestic and foreign. We are expected to assume the CDC relies upon the most advanced and cutting-edge medical science and data to make its policy decisions. However, the agency’s history of corruption and fraud contradict its own pledge, as outlined on its website. Instead of protecting the “health security of our nation,” the CDC uses bromides and meaningless pageantry to hide its true nature.

During the past year, especially in recent months, the fear-mongering spewing forth from the CDC has become virulent. It is a classic Orwellian script. The recent measles outbreak – although nowhere near as alarming as the flare-ups of bygone eras – has been seized upon as an opportunity to brainwash the public and reshape it into obedient livestock in order to increase vaccination compliance. Worse, this disinformation campaign ignores everything we know about measles infection and the failures of the MMR vaccine.

Unfortunately, we are no longer permitted to debate the pros and cons of the measles vaccine. The CDC consistently shuts down debate when its decisions are challenged.  Physicians, medical researchers, immunologists and former vaccine advocates who challenge the loose claims for vaccine safety and efficacy are frustrated and eager to publicly debate the best vaccine advocates the CDC and vaccine industry have to offer, but none will take up the challenge because the science is so clearly not on their side. The agency consistently fails to conduct and apply the gold standard in its own medical research and ignores the best independent peer-reviewed science. In short, this agency is a mouthpiece for the pharmaceutical-industrial complex and operates for its own financial advantage, rather than for the benefit of society. Its revolving doors are kept spinning with a constant influx of pharmaceutical industry and vaccine insiders. In fact the lines separating corporate influence and public health are grossly blurred and distorted. It is no surprise that documents obtained through Freedom of Information Act (FOIA) requests paint the CDC as rotten in its core and one of the greatest health threats to the nation. The agency, in Robert Kennedy Jr’s words, is a “cesspool of corruption.”

What you will never hear in the mainstream media is that there is another medical institution that is supposed to have been granted the responsibility to assure the CDC receives quality and reliable scientific research to use as the basis for its healthcare decisions.  The Institutes of Medicine (IOM) does not possess the CDC’s legislative clout; however, it represents a far superior body of scientists and researchers in their medical fields.

Founded in 1970, the Institute of Medicine falls under the charter of the National Academy of Sciences started by President Abraham Lincoln and Congress in 1863. The Academy was founded for the purpose of bringing together the nation’s best scientific minds to advise the government on scientific matters. The IOM was founded later to provide expert advice and reliable medical research to the White House and Congressional legislators to guide their decisions, keeping them informed about the social, economic and political impacts of healthcare. According to its principles, and unlike the CDC, IOM members deliberating on vaccine research and policies are expected to be independent and not represent private interests.

During a press conference this month at Yale University, Children’s Health Defense founder Robert Kennedy Jr presented data from his investigations into the CDC’s culture of medical negligence and efforts to cover up of the compelling evidence for vaccine-induced injuries, including autism. Over the course of twenty years, the IOM has monitored and reviewed the medical literature to determine the most- and least- likely injuries associated with specific vaccines and provided recommendations to the CDC. In 1991, 22 illnesses were identified, 6 were confirmed as vaccine-related and 12 remained uncertain due to insufficiently reliable studies. Those cases with confirmed causation included learning disabilities, attention deficit disorder, and childhood diabetes. This data was collected subsequent to President Ronald Reagan signing the National Vaccine Injury Compensation Act, a point when autism rates started to climb exponentially. Three years later, the IOM identified 54 medical conditions, the medical literature supported 10 diseases as vaccine-induced and 38 were uncertain. Among the confirmed illnesses were seizures, demyelinating disease, sterility, transverse myelitis and, for the first time, Sudden Infant Death Syndrome (SIDS). Again in 2011, the IOM reported a whopping 155 adverse conditions with 16 vaccine-induced injuries supported by the science, including a correlation between the DTaP vaccine and autism. Unfortunately, the IOM holds no official authority over our federal agencies; consequently, its recommendations to the CDC to further investigate vaccines’ adverse effects went unheeded. Today, nothing has changed at the CDC. Instead, the agency has dug itself into a deeper hole of secrecy and corruption. With a budget of $11.5 billion, Kennedy notes that only a pathetic $20 million is designated for vaccine safety. The CDC is crying out for a thorough public audit.

These early IOM reports are extremely valuable. They identify many of the same childhood diseases that have grown to epidemic proportions in the intervening years, and they indict vaccines as a causal factor. Yet regrettably, the IOM has recently showed signs of becoming as compromised as other health agencies. It, too, may have become another pawn of the Medical Deep State that is infiltrating every state legislative body to pass draconian immunization laws with the end goal of vaccinating Americans by lies and even threats and force if necessary.

For example, in a 2013 report on the safety of the CDC’s Childhood Immunization Schedule, the IOM gave its stamp of approval while ignoring the fact that no vaccine trial, except for a poorly designed Gardasil trial, has conducted safety tests with a scientifically valid placebo. Nor are there credible and reliable studies to support claims that no synergistic health risks arise from administering multiple vaccines concurrently. Now the IOM, too, is basing its conclusions on junk corporate science.  Its recent reports also omit reviews of the scientific literature that note the toxicity of the aluminum adjuvant used in many vaccines, including the MMR.

Recent research conducted by Dr. Chris Exley at Keele University in the UK has uncovered the pathways by which high amounts of vaccine aluminum accumulate in brain tissue rather than being excreted. High brain aluminum levels were found in deceased autistic children whose tissues were donated for his research. Autistic children can have as much as ten times the amount of aluminum lodged in the brain compared to a normal adult. Blogging on the Hippocratic Post, Exley notes that Merck refuses to make its aluminum adjuvant available for researchers to conduct independent analysis.

The CDC’s crimes are a matter of public record. These are not secrets or confidential information. The documents and voices of whistleblowers within the CDC are readily found on the internet to support all of our charges against the agency. They are readily available to anyone who wishes to investigate. Unfortunately, our media has again failed to do its job in accurately reporting on federal corruption, instead becoming an instrument of the Medical Deep State and a mouthpiece to deceive the public.

CDC misconduct includes widespread corporate nepotism favoring private pharmaceutical interests, illegal destruction of clinical data that showed a correlation between the MMR vaccine and a 250 percent increase in autism among African American boys, hiring a criminal(s) to conduct fraudulent research to conceal the neurological risks of mercury-containing vaccines, the silencing of internal officials and whistleblowers, serving as the go-between on behalf of the beverage industry concerning the World Health Organization’s restriction of sugary soft drinks, etc. The CDC has fudged firearm safety statistics; that report led Harvard University’s Injury Control Research Center director David Hemenway to declare that no one should trust the CDC’s estimates.

During the 1970s, it was the CDC’s Dr. Colleen Boyle who covered up the hideously toxic nature of Agent Orange and dioxin that thousands of Vietnam War veterans were exposed to. Although the IOM and Congress revealed Boyle’s chicanery, the agency duly rewarded her loyalty with a promotion.

The CDC and the vaccine industry have been colluding for a long time. In 2004, Congress accused the agency of operating as a public relations firm for private interests, rather than as a watchdog ensuring the integrity of vaccine science. That same year, the US Office of Special Counsel uncovered potential evidence that the CDC and pharmaceutical companies were destroying data linking the vaccine preservative thimerosal with neurological disorders. Senator Tom Coburn’s expose reveals the agency’s widespread budgetary mismanagement has wasted millions of tax dollars and concludes that the CDC cannot demonstrate it is controlling disease.

In October 2017, Congressman Bill Posey sent a letter to then-Attorney General Jeff Sessions calling on him to resume efforts to extradite and prosecute Dr. Poul Thorsen for money laundering of over $1 million from the CDC. The catch is that Thorsen was contracted by the CDC to conduct fraudulent research in Denmark that would mask any association between the vaccine preservative thimerosal and autism. In 2011, Thorsen was placed on the Inspector General’s most wanted list; nevertheless, the CDC has continued to erect obstacles to extradition efforts. More worrisome, Rep Posey discovered that for at least three years after the FBI issued its arrest warrant, the CDC and National Institutes of Health continued to collaborate with Thorsen and even joint-published more junk science together.

Another misdemeanor involved the CDC providing erroneous data to Congress about its women’s health program, WISEWOMAN, commissioned to provide preventative health services to women between 40 and 65 to reduce cardiovascular disease. Native Americans were also targeted for assistance in the program. The data was cooked and enrolled far less women than the CDC reported to Congress.

These ethical violations are systemic throughout the agency and Congress has been paralyzed in any efforts to rein in the rottenness that saturates the agency’s leadership.

In 2016, a group of scientists within the agency submitted a letter stating their concerns to the CDC’s chief of staff:

We are a group of scientists at the CDC that are very concerned about the current state of ethics at our agency. It appears that our mission is being influenced and shaped by outside parties and rogue interests…. What concerns us most is that it is becoming the norm and not the rare exception. Some senior management officials at CDC are clearly aware and even condone these behaviors. Others see it and turn the other way. Some staff are intimidated and pressed to do things they know are not right.

Out of fear of retribution, this group of CDC employees filed their complaint anonymously.

Over the years, Congressional subcommittees have voiced warnings to CDC officials to clean up their act. A House Government Reform Committee reported that both the CDC’s and FDA’s advisory committees for vaccines were thoroughly compromised with pharmaceutical conflicts of interest.  Paul Offit, the poster boy of vaccine McCarthyism and a darling of the mainstream media, participated in closed-door sessions to draft a rotavirus vaccine recommendation for a vaccine Offit co-developed and eventually sold to Merck for over $182 million.  Another voting advisory committee member held a patent on a rival rotavirus vaccine. Neither advisory committee complies with the Federal Advisory Committee Act, which requires a diversity of medical opinions; instead, the committees are stacked with corporate shills advocating for fast-tracking poorly developed vaccines with insufficient and untrustworthy safety and efficacy data to otherwise support their approval. In 2009, the Office of the Inspector General conducted an investigation of conflicts of interests within the CDC. The Office discovered that 97 percent of its advisors failed to declare their links to the pharmaceutical industry.

Consider for the moment the kinds of people who have held the CDC Directorship in recent years:

Brenda Fitzgerald MD – One of Trump’s short-lived appointments. She resigned after 5 months due to conflicts of interest with the tobacco industry and investing in a Japanese tobacco company while in office.

Tom Frieden MD – Appointed by Obama, resigned and founded the Resolve program funded by Mark Zuckerberg’s and Bill Gates’ foundations. In 2018, Frieden was charged with one count of sex abuse and a count of second degree harassment.

Julie Gerberding MD – Appointed by Bush. Following her success in getting Merck’s HPV vaccine, Gardasil, fast tracked through regulatory hurdles, she joined Merck and is now the president of its vaccine division ($2.5 million annual salary and $38 million in stock options).

The Nuremberg trials indicted Nazi doctors with crimes against humanity for conducting inhumane experiments with highly toxic drugs on innocent people. Yet the Code generated at Nuremberg does not apply to modern vaccines such as the HPV vaccine Gardasil. Dr. Bernard Dalbergue used to work for Gardasil’s manufacturer Merck. In an interview in the French magazine Principes de Sante, Dalbergue said Merck fully knows the vaccine is worthless in protecting against cervical cancer. He stated, “I predict that Gardasil will become the greatest medical scandal of all times because at some point in time the evidence will add up to prove that this vaccine, technical and scientific feat that it may be, has absolutely no effect on cervical cancer…. The very many adverse effects which destroy lives and even kill, serve no other purpose than to generate profit for the manufacturers.”  Meanwhile, the National Institutes of Health profits from Gardasil sales with royalties and will benefit more as the vaccine is mandated by state legislators.

We have deep reservations towards accusing the federal health agencies of engaging in a revival of eugenic technologies. But we ask readers to consider a recent analysis published in the Journal of Toxicology and Environmental Health that reveals a lowered probability of pregnancy among American women between 25 and 29 years of age who have received the HPV vaccine. Since the launch of Gardasil, birth rates have been falling. For women aged 25 to 29 – within the range of the new Gardasil Generation – rates fell from 118 in 1000 to 105. This may appear coincidental. However, 60 percent of unvaccinated women became pregnant at least once compared to only 35 percent who received the HPV vaccine. For married women, 75 percent who were unvaccinated conceived versus 50 percent of vaccinated women.  The study suggests that if 100 percent of women had received the HPV vaccine, there would be 2 million more women likely infertile.

We have reported in the past how the CDC operates more like a private intelligence and surveillance firm rather than a federally funded public health service. In the meantime, epidemics of autism, neuro-developmental disorders, autoimmunity, childhood diabetes, febrile seizures, asthma and allergies roll on and federal health officials embrace the superstitions of vaccine magic and reside in a culture of medical denialism.

Finally, there is a fundamental question.

Would you hire someone with such an extensive rap sheet to care for your child, let alone a newborn infant?  Would you trust them to undertake the correct measures in an emergency, or use sound judgment to assure your child’s well-being?  For the hundreds of thousands of vaccine-damaged children, the CDC remains a felon on the loose. And the rest of our government is less competent than inebriated Keystone cops to authorize a thorough housecleaning. The agency displays no sincere interest in your child’s well-being and health, nor those of any American for that matter. And the mainstream media, every major network, newspaper and magazine, are similarly unconscionably complicit in preserving the CDC’s culture of deception. The entire media should be stamped with a warning as life-threatening dangers to the public health.

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If Truth Be Told About Unreported Vaccine Adverse Reactions: Do VAERS Reports Represent Demographic Statistical Actuality?

By Catherine J. Frompovich

Ever since the 1980s I have been researching vaccine data, but I cannot seem to figure out – for the life of me – how many actual adverse reactions experienced by vaccinees are reported to VAERS, since there are so many data variables, plus estimated figures bandied around, as you will soon learn.

The vaccine adverse reactions reporting conundrum apparently gained some legitimacy with this report:

VAERS MAY ACCOUNT FOR ONLY 1 PERCENT OF ACTUAL VACCINE INJURIES [Nov 2, 2015]

But how many children have vaccine reactions every year? Is it really only one in 110,000 or one in a million who are left permanently disabled after vaccination? Former FDA Commissioner David Kessler [1] observed in 1993 that less than 1 percent of doctors report adverse events following prescription drug use. There have been estimates that perhaps less than 5 or 10 percent of doctors report hospitalizations, injuries, deaths, or other serious health problems following vaccination. The 1986 Vaccine Injury Act contained no legal sanctions for not reporting; doctors can refuse to report and suffer no consequences.

Even so, each year about 12,000 reports are made to the Vaccine Adverse Event Reporting System; parents as well as doctors can make those reports. However, if that number represents only 10 percent of what is actually occurring, then the actual number may be 120,000 vaccine-adverse events. If doctors report vaccine reactions as infrequently as Dr. Kessler said they report prescription-drug reactions, and the number 12,000 is only 1 percent of the actual total, then the real number may be 1.2 million vaccine-adverse events annually.   [1] [CJF emphasis]

— Barbara Loe Fisher, Co-founder & President  National Vaccine Information Center (NVIC)

Now here’s where things can get somewhat “squirrelly,” I think.  In checking CDC/FDA and the feds websites, I find varying explanations and numbers for estimated yearly VAERS reports.

Since 1990VAERS has received over 123,000 reports as of June 14, 2014
[VAERS-1 Form used from 1990 to June 30, 2017]
Source: FDA

In recent years VAERS has received approximately 40,000 U.S. reports annually.  
[VAERS Form 2.0 was implemented June 30, 2017.]
Source: Federal Register

However by law, healthcare professionals must Report Vaccine Reactions!  

And still, MDs, nurses and others, who should know their legal responsibilities as licensed healthcare professionals, DO NOT file vaccine damage reports with VAERS!  What are they hiding, or whom are they protecting?

On the other hand, anyone who has experienced an adverse event after receiving a vaccine CAN and SHOULD file the proper VAERS report (Form 2.0) at this HHS website Report an Adverse Event.

Now here’s an example of where I feel almost like a cat chasing its tail in trying to figure out VAERS.

I downloaded this data set, which apparently is a sophisticated Excel spreadsheet.  Columns A to G have these designations:

VAERS_ID RECVDATE STATE AGE_YRS CAGE_YR CAGE_MO SEX

However, scrolling down the left column designated A “VAERS ID,” the numbering system seems to be an ongoing sequence that started with ID No. 794156 on 1/1/2019 and ends with ID No. 801633 as of sometime in February 2019.  Would that mean that 7745 adverse reports were filed from January 1, 2019 to sometime in February 2019?

If that be the case, then how does the above numbering system fit in with the following reported data?

A. Since 1990VAERS has received over 123,000 reports as of June 14, 2014
B. In recent years [2015 to 2019?] VAERS has received approximately 40,000 U.S. reports annually
C. 40,000 reports a year times 4 years (2015-2018) equals 160,000 to be added to 123,000 (2014) equals 283,000 reports; so why begin Jan. 1, 2019 with 794,156?
D. If 7745 adverse reports were filed from January 1, 2019 to sometime in February 2019,then what explains ID No. 801633 as of sometime in February 2019?
E. If 7745 reports represent approximately one-eighth (1/8) of 2019 calendar days, can we hypothesize 61960 total VAERS reports for all of 2019—not 40,000?
F. The above numbering system seems to indicate, and represent, more adverse events reported since the mandatory increases in the CDC vaccine schedule.

If I am correct in my assumptions about the VAERS ID numbering system, there probably is substantial proof that 801633 Adverse Events Reports had been filed to sometime in February 2019 since 1990.

Those numbers indicate there ARE adverse reaction vaccine problems, which the CDC and FDA do not seem to acknowledge, all while cataloging VAERS as a post-marketing product-efficacy surveillance system.

And even more alarming, I think, when taking the above ‘logic’ a step further to factor into consideration Dr. Kessler’s estimation of less than 1% being reported, what could be the “real life” number of experiences by consumers to February 2019?  Good question?

My calculator figured 80 million 163 thousand 3 hundred probable adverse reactions may have occurred from 1990 to sometime in February 2019, which could [or should] have been reported to VAERS.

Sadly, consumers probably may never know the accurate data sets until there is total transparency at every level of vaccine consensus science and adverse events reporting.

Reference:

[1] https://www.medscape.org/viewarticle/588757

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If Truth Be Told About The SV-40 Cancer Virus In The Original Polio Vaccines Given To Millions Of American Children

By Catherine J. Frompovich

The current “police state” actions being implemented regarding vaccination dissenters is due to the public’s mistrust of the CDC/FDA/Big Pharma consensus science regarding vaccines unknown viruses and neurotoxic ingredients causing adverse effects in children’s health, which has an historical, plus congressional hearing validation, anyone who values good health and well children must consider seriously.

Merck’s premiere vaccine inventor, Dr. Maurice Hilleman, was astute enough to realize something was amiss with the production of vaccines, which he documents in the video below.

The Polio Vaccine Has Cancer Virus, SV40, According to Dr. Maurice Hilleman
10:37 minutes


https://youtu.be/1-XZs53vZzw?t=6

Widget not in any sidebars

When he spoke about bringing the monkeys over from Africa, which they used to manufacture the polio vaccine, he had this to say, “I brought African greens in. I didn’t know we were importing AIDS virus at the time.”[1]

Dr. Hilleman stated, “Yellow fever vaccine had leukemia virus in it. This was in the day of very crude science. [1]

If you think the above was something “of a fluke” or a “figment of conspiracy theorists imaginations,” then you absolutely ought to read the U.S. Government Printing Office online published report of the September 10, 2003 Hearing of the Subcommittee on Human Rights and Wellness of the Committee on Government Reform of the House of Representatives of the 108th Congress wherein Congressman Dan Burton is on public record saying:

There is no dispute that millions of Americans received polio vaccines that were contaminated with the virus called Simian Virus 40, or SV-40. There also is no dispute that SV-40 is capable of causing cancer, but there is a major dispute as to how many Americans may have received the contaminated vaccine, with estimates ranging from 4 million to 100 million people. There is also a major dispute as to when the polio vaccine supply got cleaned up. In addition, nobody knows how many people got sick or died because of the contaminated vaccines.

However, Dr. James Goedert, Chief of Viral Epidemiology, National Cancer Institute, provided an answer as to when the polio vaccine got cleaned up:

In addition, using PCR technology, the FDA itself found no SV-40 DNA molecules in lots that were released between 1972 and 1996.

When did you or your children receive the polio vaccine?

Can the SV-40 cancer virus be lurking within your body?

Why do I say that?

Because the Journal of Infectious Diseases published the article “Simian Virus 40 and Human Disease” wherein this was discussed:

The reported presence of SV40 in tumors in individuals born after 1963 would seem to imply that SV40 is now established as a human infection circulating in communities via person-to-person contact [8]. Other investigators have been skeptical of these claims [9–12]; several groups have not been able to detect SV40 sequences in the aforementioned tumors [13–20], and epidemiologic studies have not revealed an increased risk of these cancers in populations exposed to SV40-contaminated poliovaccines or adenovirus vaccines.

[8] Vilchez RA, Butel JS, Emergent human pathogen simian virus 40 and its role in cancer, Clin Microbiol Rev, 2004, vol. 17 (pg. 495-508)

[CJF emphasis]

In view of the cancer epidemic of recent years, one has to wonder what role, if any, the SV-40 cancer virus in the early polio vaccine had, or is implicated in current cancer demographics, especially in older individuals who received the polio vaccine as a child.

I’d like to point out that FDA used the Polymerase chain reaction (PCR) analysis, a test FDA will not permit to be used to test for determining adverse mitochondrial proclivities (reactions) from mandatory vaccines prior to receiving vaccines/vaccinations, especially in infants whose immune systems are not developed fully until around two years of age!

In those individuals with mitochondrial proclivities, vaccination can be equivalent to immune system castration!

The FDA PCR directive, alone, ought to be considered as criminal activity, since such FDA actions deliberately – by the omission of PCR testing as a routine prophylactic procedure – contributes directly to any vaccine adverse reactions infants, toddlers, teens and adults would experience. Therefore, FDA ought to be held accountable, plus prosecuted, for malfeasance in the management of infectious disease protocols, in my opinion!

References:

[1] unhoodwinked Published on Jan. 9, 2015

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IF Truth Be Told About Vaccines! Risk Of SEIZURES After MMR & DTP Vaccinations Exist Per CDC Vaccine Safety Datalink Working Group

By Catherine J. Frompovich

How dare they?

What colossal nerve?

Their own published study PROVED the risk(s) for seizures exist after MMR and DTP vaccinations, but they did not make that life-altering event a mandatory “informed consent” item MDs and all vaccine pushers must disclose to parents, plus all intended MMR and DPT vaccinees—whatever their age would be! Adults now have to be concerned about that as a health issue with the mandatory Adult Vaccination Protocol CDC/FDA want to implement!

Nine members of the CDC Vaccine Safety Datalink Working Group – along with 10 other healthcare professionals, i.e., PhDs, MDs and MPHs degrees – confirm there are risks of seizures after the MMR and DTP vaccines, and the CDC/FDA do nothing except concoct lies!

Here is “Secret CDC Verstraeten study shows neurological developmental disorders with mercury in vaccines.”

Is the above paper the original 1999 Verstraeten study that needed to be sanitized, revised and reworked, because it found health issues after MMR and DPT vaccinations, as was discussed at a secret gathering of 52 Pharma, CDC/FDA and WHO officials, who met at the Simpsonwood Conference Center in Georgia in June [7-8] of 2000, to collude in secret to determine how to do “damage control” and create a plausible solution to an apparent vaccine adverse reaction or contraindication: the MMR and DTP vaccines can and do cause seizures.

Wasn’t Dr. Verstraeten tasked by the Simpsonwood meeting consensus to rework his study? and, oh boy, didn’t he!

By the way, here’s the transcript – all 286 pages – for that Simpsonwood meeting; note what various MDs had to say about the original findings, and yet they still believe the consensus science and even promote it.

Is this Verstraeten’s reworked paper?

Is this the vaccinology ‘science’ paper which, apparently, set the tarnished ‘gold standard’ for corrupting all vaccine data studies henceforth?

August 30, 2001

“The Risk of Seizures after Receipt of Whole-Cell Pertussis or Measles, Mumps, and Rubella Vaccine”

William E. Barlow, Ph.D., Robert L. Davis, M.D., M.P.H., John W. Glasser, Ph.D., M.P.H., Phillip H. Rhodes, Ph.D., Robert S. Thompson, M.D., John P. Mullooly, Ph.D., Steven B. Black, M.D., Henry R. Shinefield, M.D., Joel I. Ward, M.D., S. Michael Marcy, M.D., AND Frank DeStefano, M.D., Virginia Immanuel, M.P.H., John A. Pearson, M.D., Constance M. Vadheim, Ph.D., Viviana Rebolledo, B.S., Dimitri Christakis, M.D., M.P.H., Patti J. Benson, M.P.H., Ned Lewis, M.P.H., and Robert T. Chen, M.D.et al., for the Centers for Disease Control and Prevention Vaccine Safety Datalink Working Group

This cohort study was conducted at four large health maintenance organizations and included reviews of the medical records of children with seizures. We calculated the relative risks of febrile and nonfebrile seizures among 679,942 children after 340,386 vaccinations with DTP vaccine, 137,457 vaccinations with MMR vaccine, or no recent vaccination. Children who had febrile seizures after vaccination were followed to identify the risk of subsequent seizures and other neurologic disabilities.

Results

Receipt of DTP vaccine was associated with an increased risk of febrile seizures only on the day of vaccination (adjusted relative risk, 5.70; 95 percent confidence interval, 1.98 to 16.42). Receipt of MMR vaccine was associated with an increased risk of febrile seizures 8 to 14 days after vaccination (relative risk, 2.83; 95 percent confidence interval, 1.44 to 5.55). Neither vaccination was associated with an increased risk of nonfebrile seizures. The number of febrile seizures attributable to the administration of DTP and MMR vaccines was estimated to be 6 to 9 and 25 to 34 per 100,000 children, respectively. As compared with other children with febrile seizures that were not associated with vaccination, the children who had febrile seizures after vaccination were not found to be at higher risk for subsequent seizures or neurodevelopmental disabilities.

Conclusions

There are significantly elevated risks of febrile seizures after receipt of DTP vaccine or MMR vaccine, but these risks do not appear to be associated with any long-term, adverse consequences.

[Note those infamous “wiggle-room” words: “do not appear to be associated with,” which is NOT scientific proof; it’s consensus science, for which CDC/FDA must be held accountable in misleading health consumers.]

Publications from that sad day forward in peer-review studies, successfully have been hoodwinking consumers regarding health issues; numerous disciplines, and even politics, seemingly have followed a structured corporate “damage control” line. How come?

A current and parallel unfortunate happening is the recent Ethiopian 737 airline crash killing 157 on board, following another similar incident, i.e., Lion Air flight 610, October 29, 2018. Why were those planes allowed to fly? Why was the USA the last to issue a no fly directive? Shouldn’t we have been the first?

It seems as if corporations are in business to:

  • Be part of the New World Order control mechanism, or
  • Become giant money-making behemoths who, then, can flex their fiscal muscles in lobbying Congress to get their corporate policies/cultures/marketing dreams ensconced in statutory law.

Currently, consumers globally are held ‘captives’ by corporations!

A perfect example is what’s going on within Big Pharma pharmaceutical pricing politics; the microwave tech industry pushing 5G and possible 6G without safety studies performed relating to human health and the environment; the implementation of the Internet of Things, and Transhumanism.

Here’s a question, which needs to be asked, I think: Is there any similarity between how corporations act and the original definition of “fascism” as designated by its founder Benito Mussolini?

However, it seems the definition of fascism, though, is being redefined as conservative value politics—as are most cultural memes—in the current climate of “political correctness.” Furthermore, I’d go as far as to say that we have no one to thank for that except the totally dysfunctional U.S. Congresses, who sold out their oversight rights to corporate lobbyists ever since the passage of the National Childhood Vaccine Injury Act. The National Childhood Vaccine Injury Act (NCVIA) of 1986 (42 U.S.C. §§ 300aa-1 to 300aa-34) was signed into law by United States President Ronald Reagan as part of a larger health bill on Nov 14, 1986.” (Wikipedia)

To correct things, that 1986 “get out of jail free card” for vaccine makers has to be rescinded!

Catherine J Frompovich (website) is a retired natural nutritionist who earned advanced degrees in Nutrition and Holistic Health Sciences, Certification in Orthomolecular Theory and Practice plus Paralegal Studies. Her work has been published in national and airline magazines since the early 1980s. Catherine authored numerous books on health issues along with co-authoring papers and monographs with physicians, nurses, and holistic healthcare professionals. She has been a consumer healthcare researcher 35 years and counting.

Catherine’s latest book, published October 4, 2013, is Vaccination Voodoo, What YOU Don’t Know About Vaccines, available on Amazon.com.

Her 2012 book A Cancer Answer, Holistic BREAST Cancer Management, A Guide to Effective & Non-Toxic Treatments, is available on Amazon.com and as a Kindle eBook.

Two of Catherine’s more recent books on Amazon.com are Our Chemical Lives And The Hijacking Of Our DNA, A Probe Into What’s Probably Making Us Sick (2009) and Lord, How Can I Make It Through Grieving My Loss, An Inspirational Guide Through the Grieving Process (2008)

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