By Anna Von Reitz
1. You begin your life as “one of the free, sovereign, and independent people of the United States”—- a Virginian, Minnesotan, Texan, etc….
By Anna Von Reitz
1. You begin your life as “one of the free, sovereign, and independent people of the United States”—- a Virginian, Minnesotan, Texan, etc….
Note from the World Mercury Project Team: Following is Part Two in a seven-part series of Vera Sharav’s in-depth exposé of the complex and widespread corruption that exists in the vaccination program. Her investigation has uncovered decades-long fraudulent activity that has permeated the vaccine industry. Sharav’s research is a must-read by those in our community because it explains the intricate groundwork that has led us to the debacle we are now living with – an epidemic of sick children.
You can read part one here.
Principal reports authored by scientists at the U.S. Centers for Disease Control and Prevention and CDC-sponsored reports published in the most influential medical journals are shown to be the product of scientific fraud and malfeasance by high-level CDC officials. The internal CDC documents include emails, memoranda, and transcripts of meetings and conference calls, are an irrefutable record revealing how key CDC studies and CDC-commissioned studies were shaped by use of illegitimate methods, including data manipulation, selective inclusion, and deletion of data from the published reports.
To begin with, as a senior CDC scientist, Dr. Tom Verstraeten pointed out in an email that the Danish population studies – that compared Danish vs. US autism prevalence rates – used non-comparable populations:
As will be documented below, mainstream academics accepted the published claimed findings of the CDC-sponsored Danish epidemiological studies without further examination. However, astute, skeptical, independent critics – both scientists and others – reviewed those pivotal studies in detail. These critics reported that the scientific integrity of those studies was undermined by statistical manipulation through which the MMR and thimerosal were exonerated as a causal contributor to autism.,
“when CDC officials including Coleen Boyle, Marshalyn Yeargin-Allsopp, Joanne Wojcik, and Diana Schendel became aware in 2009, that Poul Thorsen failed to obtain legally required permission for the autism biological and genetic data projects, these CDC employees participated in a cover-up with the Danish grantees.”
“the use of thimerosal-free DTaP, Hib, and hepatitis B vaccines … case-control studies examining the potential link between neurodevelopmental disorders and thimerosal-containing vaccines… further analysis of neurodevelopmental outcomes… research on how children, including those diagnosed with neurodevelopmental disorders, metabolize and excrete metals, particularly mercury… research to identify a safe, effective, and inexpensive alternative to thimerosal”
CDC responded by stating the agency was “gravely troubled by the recommendation” of the PHS and the AAP, and ignored the IOM recommendations. CDC dithered, and continued to recommend vaccines containing mercury, exposing millions of infants and children in the US to massive doses of thimerosal. CDC officials did so, with the endorsements of the FDA Advisory Committee on Immunization Practices, and the Immunization Safety Committee of the Institute of Medicine. (See CDC Thimerosal Timeline 1999-2010)
In 2000, the Resource Conservation and Recovery Act (RCRA) authorized the Environmental Protection Agency (EPA) to set regulatory policy for the disposal of medications that are known environmental hazards. These are called hazardous pharmaceutical wastes. These include: “pharmaceutical with heavy metals, including the preservative thimerosal.”
An EPA-sponsored biological study (2005) by Dr. Thomas Burbacher and colleagues at the University of Rochester compared the biological (toxicokinetic) effect of consumed methylmercury to the effect of Hg (inorganic mercury) in vaccines containing thimerosal in infant monkeys. The seventeen monkeys assigned to the thimerosal group were vaccinated in accordance with the typical CDC recommended vaccination schedule. Those 17 infants retained “a much higher proportion of inorganic Hg in the brain (up to 71% vs. 10%) [compared to infants who ingested mercury]:
“A higher percentage of the total Hg in the brain was in the form of inorganic mercury for the thimerosal-exposed infants (34% vs 7%). There was a much higher proportion of inorganic Hg in the brain of thimerosal infants than MeHg infants (up to 71% vs. 10%).
Absolute inorganic Hg concentrations in the brains of the thimerosal-exposed infants were approximately twice that of the MeHg infants. Interestingly, the inorganic fraction in the kidneys of the same cohort of infants was also significantly higher following i.m. thimerosal than oral MeHg exposure (0.71±0.04 vs. 0.40±0.03). This suggests that the dealkylation of ethylmercury is much more extensive than that of MeHg.”
Despite a body of scientific evidence, CDC continues to broadcast its reassuring, but untenable claim:
“There is no evidence of harm caused by the low doses of thimerosal in vaccines, except for minor reactions like redness and swelling at the injection site.” Thimerosal contains ethylmercury, which is cleared from the human body more quickly than methylmercury, and is therefore less likely to cause any harm.” (CDC website)
CDC and its bevy of vaccine stakeholders ignore the scientific evidence and the fact that most of the consumed mercury in fish is excreted. The documented risks of Thimerosal – especially for young children and unborn neonates – who are at increased risk of neurological brain damage/autism – led to the eventual removal of Thimerosal from childhood vaccines – although CDC never conceded that fact.
However, some influenza vaccines contain 250 times the mercury level that EPA uses to classify hazardous pharmaceutical waste. What’s more, since 2002, CDC expanded its recommendation for the flu vaccine. In 2010, CDC recommended the flu shot for very young infants (6 and 7 months old), and an annual flu vaccine for everyone – including children and pregnant women.
The authors of a recently published review, Thimerosal: Clinical, Epidemiologic and Biochemical Studies (2015) point out, that despite the existence of approved, effective preservatives, Thimerosal continues to be used in some vaccines administered to infants, children, and pregnant women.
As a consequence of CDC recommendations, the cumulative exposure of US children to Thimerosal remains relatively high. In developing countries, the amount of Thimerosal in childhood vaccines has not been reduced and the harmful consequences are documented.
The CDC Verstraeten study findings were concealed from all but a small circle of scientists. CDC officials conspired to overturn the evidence of the thimerosal-autism risk documented by its own scientists.
A transcript of a January 2001 closed-door meeting of the IOM Immunization Safety Review Committee (obtained in 2011 during Court proceedings) records the discussion centered on the content of a CDC draft report before the IOM committee ever examined the evidence. The chair of the committee, Dr. Marie McCormick, of the Harvard School of Public Health, and IOM scholar, Dr. Kathleen Stratton, the study director, specified to committee members what conclusions they were expected to sign off on – no matter what the evidence shows:
“CDC wants us to declare [sic] these things are pretty safe on a population basis.” [p33] “We are not ever going to come down that [autism] is a true side effect.”
Dr. Kathleen Stratton: “The point of no return, the line we will not cross in public policy is to pull the vaccine, [or] change the schedule. We could say it is time to revisit this, but we would never recommend that level. Even recommending research is recommendations for policy. We wouldn’t say compensate, we wouldn’t say pull the vaccine, we wouldn’t stop the program.” [p74]
The influential IOM committee backed away from its 2001 recommendations and delivered the report that CDC had dictated and stressed that raising questions about the safety of vaccines poses the danger of rejection of vaccines:
“The committee concludes that the body of epidemiological evidence favors rejection of a causal relationship between the MMR vaccine and autism. The committee also concludes that the body of epidemiological evidence favors rejection of a causal relationship between thimerosal-containing vaccines and autism…
“Using an unsubstantiated hypothesis to question the safety of vaccination and the ethical behavior of those governmental agencies and scientists who advocate for vaccination could lead to widespread rejection of vaccines… ” Immunization Safety Review: Vaccines and Autism (2004)
The “body of evidence” that the IOM review relied on was 5 CDC-funded fatally flawed epidemiological studies; several of these were found to be fraudulent.  Another study relied on the UK General Practice Research Database (GPRD) whose reliability is in doubt.
“there was no evidence that thimerosal exposure via DTP/DT vaccines causes neurodevelopmental disorders.” The IOM reviewers failed even to consider FDA’s risk assessment: An Assessment of Thimerosal Use in Childhood Vaccines (2001) which cautioned:
“some infants may be exposed to cumulative levels of mercury during the first 6 months of life that exceed EPA recommendations. Exposure of infants to mercury in vaccines can be reduced or eliminated by using products formulated without thimerosal as a preservative.”
Furthermore, the IOM committee refused to review pre-publication drafts of rigorous biological studies. These included scientists from Columbia University (Molecular Psychiatry, 2004); University of Arkansas (NeuroToxicology, 2005); Northeastern University (Molecular Psychiatry, 2004); a U.S. epidemiological study by Johns Hopkins University (Pediatrics, 2005); Harvard University (Neuroscientist, 2005); and the University of Washington (Environmental Health Perspectives, 2005).
The committee rushed to issue its report exonerating Thimerosal. The IOM report lent validity to irrelevant epidemiologic studies, government vaccination policies, and provided the National Vaccine Injury Compensation Program (NVICP) with the rationale against compensation for autism. The conclusions reached by the IOM Committee were pre-determined, as were the studies upon which it relied. The committee delivered the findings that it was commissioned and paid to deliver.
This dishonest review by the IOM panel demonstrates the lack scientific integrity of a report issued by the Institute of Medicine, further validating public distrust of “authoritative” government and quasi-government medical institutions. Nevertheless, the influence of this flawed report extends far and wide.
Dr. Robert Chen, Chief of Vaccine Safety for CDC’s National Immunization Program (NIP) initiated the Brighton Collaboration. It was launched in 2000, by members of the Cochrane Collaboration: Tom Jefferson, Harald Heijbel, Ulrich Heininger, Elisabeth Loupi, with funding obtained from the CDC and the WHO.
In an editorial in the BMJ Journal of Epidemiology and Community Health Online (June 2000), Dr. Jefferson urged the UK government to launch a computerized vaccine exposure and outcome database such as the one the US CDC maintains (i.e., Vaccine Safety Datalink, VSD) in order to rapidly counteract public concern.
“Since the publication of the Wakefield study on 28 February 1998, public concern fueled by extensive media coverage caused a steady decline in MMR coverage in parts of the United Kingdom, with a subsequent risk of a decline in herd immunity and resurgence in morbidity.”
“As usual with vaccine “scare stories,” there was a delay between publication of the initial case series and that of population-based causal assessment study. During this time, declining coverage took place.”
“The impact on parents of a perceived causal link with a chronic disease that could threaten the life and wellbeing of their children is understandably great. Inevitably, in a proportion of cases the worry and emotion spills over into a threat of legal action against governments, manufacturers or individuals. This has the effect of taking the matter outside the scientific and healthcare arena and into the realm of the judiciary.” 
It would appear that Dr. Jefferson was unaware of the Verstraeten Vaccine Safety Datalink population-based study:
WMP NOTE: This concludes Part Two. Part Three of the Seven-Part series is entitled: Gaining Control of Vaccine-Related Information: Establishing an Infrastructure. Previously published articles: Sharov’s Introduction outlined her well-researched and documented belief that, “Public health officials and the medical profession have abrogated their professional, public, and human responsibility, by failing to honestly examine the iatrogenic harm caused by expansive, indiscriminate, and increasingly aggressive vaccination policies.” Part Onefocused on how the Centers for Disease Control and Prevention (CDC) and the vaccine industry controlled vaccine safety assessments, controlled the science of vaccines and controlled the scientific and mass channels of information about vaccines.
More about the author: Vera Sharav is a Holocaust survivor and a fierce critic of the medical establishment. This article was originally published at www.ahrp.org. Stat news recently published an article about her and her work.
Written by Vera Sharav
Note from the World Mercury Project Team: Following is Part One in a seven-part series of Vera Sharav’s in-depth exposé of the complex and widespread corruption that exists in the vaccination program. Her investigation has uncovered decades-long fraudulent activity that has permeated the vaccine industry. Sharav’s research is a must-read by those in our community because it explains the intricate groundwork that has led us to the debacle we are now living with – an epidemic of sick children.
The exponential increase in the autism / autism spectrum prevalence rate since 1985 (1 in 2,500) to 2016 (1 in 45) is evidence of an epidemic, not, as the deniers will have it, “an optical illusion” or “a statistical mirage”
“today a million and more Americans, almost all under thirty, have been formally diagnosed with autism…Most with an autism diagnosis will never [lead normal lives] or be responsible for their health and welfare. Both the increase and the burden it imposes are widely recognized by thousands of parents and frontline professionals such as nurses and teachers. Yet some of the most prominent and powerful people in medicine, the media, and government deny it.” [DENIAL: How Refusing to Face the Facts about Our Autism Epidemic Hurts Children, Families, and Our Future, Mark Blaxil and Dan Olmsted (2017)]
The focus of this appendix is how the Centers for Disease Control and Prevention (CDC) and the vaccine industry control vaccine safety assessments, control the science of vaccines and control the scientific and mass channels of information about vaccines. These primary stakeholders gained control by establishing an elaborate web of collaborating institutional partnerships which they fund. The collaborating institutional stakeholders include:
Numerous additional industry front groups are popping up on social media to spread vaccine propaganda, such as the European Health Parliament (EHP, situated in Brussels, created in 2017). EHP is bankrolled by Johnson and Johnson and is affiliated with Google, Politico and others. [Appendix 10 is being updated. It will publish shortly.]
All of these institutions became de facto stakeholders in promoting vaccination policies while presenting themselves as independent authoritative sources of information about vaccine safety.
Through this elaborate network of collaborative partnerships, industry gained global control of vaccine safety assessments – which are applied as the single standard, used mostly to rule out a causal relationshipbetween vaccination and serious adverse events following vaccination. These centrally controlled assessments are applied indiscriminately in all cases, disregarding individual human susceptibility factors.
One of the intended features of these collaborating partnerships is to camouflage the identity of the funding source for vaccine research and professed independent reviews of vaccine research. Medical journals, as the editor-in-chief of The Lancet, Dr. Richard Horton acknowledged, “devolved into information laundering operations for the pharmaceutical industry.” Indeed, the BMJ (British Medical Journal) entered into undisclosed partnership agreements with both major vaccine manufacturers. In 2008, BMJ and Merck entered into partnership and in 2016, BMJ and GlaxoSmithKline formed a partnership as well. Additionally, vaccine stakeholders control the vast channels of propaganda – including Google, which has formed a partnership with GlaxoSmithKline.
The financial interest of these collaborating partnerships conflicts with the tenets of medical ethics and scientific integrity – such as transparency and independent assessment of the data. The consequences of these ill-suited partnerships are demonstrated by evidence of corrupt vaccine safety assessments; evidence of harm following vaccination is either concealed or defined as non-related; journal publications are corrupted by fraudulent reports, and honest scientific findings are suppressed. The entire web of vaccine stakeholder- collaborations is geared toward issuing uniform vaccine safety pronouncements that promote vaccination policies crafted to ensure high vaccination rates, translating to ever higher profit margins.
Much of the evidence is documented in thousands of internal CDC documents (some were obtained in 2011); additional CDC internal documents were obtained in July 2017. The evidence is also documented in transcripts of closed-door meetings, such as the Epidemic Intelligence Service (EIS) at Simpsonwood (2000); the Institute of Medicine Committee on Immunization Safety Review (2001); and the UK Joint Committee on Vaccination and Immunisation (JCVI, 1990). These documents were obtained under the Freedom of Information Act (FOIA). Evidence was also gathered in the course of a criminal investigation of Dr. Poul Thorsen by the U.S. Inspector General, Department of Health and Human Services (HHS).
In 1974, the FDA convened a panel of experts to conduct a comprehensive review of the safety and effectiveness of over-the-counter medicines. One facet of the review was OTC drugs that contained mercury whose function was to kill bacteria to prevent infection. In 1980, the Advisory Review Panel submitted its report to the FDA, having reviewed 18 products containing mercury. It found the products either unsafe or ineffective. The report cited several studies demonstrating human hypersensitivity to thimerosal:
“mercury compounds as a class are of dubious value for anti-microbial use. Mercury inhibits the growth of bacteria, but does not act swiftly to kill them.”
“The Panel concludes that thimerosal is not safe for OTC topical use because of its potential for cell damage if applied to broken skin, and its allergy potential. It is not effective as a topical antimicrobial because its bacteriostatic action can be reversed.”
After the determination by the FDA advisory committee, Eli Lilly chose to cease production of Thimerosal-containing products. Despite the evidence, Thimerosal continued to be added to vaccines. In 1990, Professor Hans Wigzell, Rector of the Karolinska Institute, Sweden, and member Nobel Committee for Physiology or Medicine, wrote “Difficult to Substitute Mercury as a Preservative in Bacterial Vaccines”, in which he recommended that:
“a study [be conducted] to show if there is a difference in general toxicity when uptake of mercury is from the stomach-intestines or after injections…This should be studied in relation to the tremendous large number of subjects vaccinated with preparations containing thimerosal sodium; Our goal is to develop, as soon as possible, vaccines completely free of mercury.”
In 1991, Dr. Maurice Hilleman, an internationally renowned Merck vaccinologist, wrote a memo to the president of Merck’s vaccine division stating:
“6-month-old children who received their shots on schedule would get a mercury dose up to 87 times higher than guidelines for the maximum daily consumption of mercury from fish. When viewed in this way, the mercury load appears rather large. The key issue is whether thimerosal, in the amount given with the vaccine, does or does not constitute a safety hazard. However, perception of hazard may be equally important.” 
The FDA delayed issuing its final rule on thimerosal until 1998, stating: “safety and effectiveness have not been established for the ingredients (mercury based preservatives)… manufacturers have not submitted the necessary data in response to earlier opportunities.”The rule, however, applied only to OTC products.
In 1991, Dr. Peter Aaby, Director of the Bandim Health Project, a demographic surveillance system (in Guinea-Bissau, West Africa), which is affiliated with the Statens Serum Institute, identified non-specific adverse vaccine effects which go beyond the specific protective effects of the targeted disease. He noted that these non-specific effects can be beneficial or harmful. Dr. Aaby has conducted a series of comparative “natural studies” of vaccinated and unvaccinated children in high-mortality regions in rural Africa, that consistently confirmed that:
“Though a vaccine protects children against the target disease it may simultaneously increase susceptibility to unrelated infections.”
The 1999 CDC study sought to determine the relative risk for infants following exposure to thimerosal-containing childhood vaccines was conducted by Dr. Thomas Verstraeten and three CDC colleagues who examined the evidence documented in CDC’s Vaccine Safety Datalink (VSD). They analyzed the medical records of 400,000 infants born between 1991 and 1997 that were maintained by four HMOs and assessed the risk of autism for the children at different ages.
This was a scientifically solid study; it provided scientific documentation that: exposure to thimerosal during the first month of life increased the relative risk of autism by 7.6 i.e., 760%.
The VSD data revealed additional risks as well: 1.8 increased relative risk for a neurodevelopmental disorder; 2.1 relative risk for speech disorder; and 5-fold increased relative risk for a nonorganic sleep disorder. The evidence documents that infants exposed to vaccines laced with thimerosal during the first month of life are at an alarmingly high increased risk of serious harm.
In December 1999, Dr. Verstraeten sent an email to his co-authors and CDC colleagues, Dr. Robert Davis and Dr. Frank DeStefano; the subject line was “it just won’t go away”. The email attachments included four tables with relative risk data and the Abstract of their study findings, that he was submitting for a presentation, at the high level (by invitation only) meeting, convened by CDC’s Epidemic Intelligence Service, at Simpsonwood Retreat Center in Georgia (2000).
The title of their study: “Increased Risk Of Developmental Neurologic Impairment After High Exposure To Thimerosal-Containing Vaccine In First Month Of Life.”
The meeting was chaired by Richard Johnston, M.D., an immunologist and pediatrician (University of Colorado) who stated:
“The data on its toxicity (shows) it can cause neurologic and renal toxicity, including death. We learned [sic] a number of important things about aluminum, and I think they also are important in our considerations today.”
“Aluminum salts are important in the formulating process of vaccines, both in antigen stabilization and absorption of endotoxin. Aluminum and mercury are often simultaneously administered to infants, both at the same site and at different sites.”
“However [sic] there is absolutely no data, including animal data, about the potential for synergy, additively or antagonism, all of which can occur in binary metal mixtures that relate and allow us to draw any conclusions from the simultaneous exposure to these two salts in vaccines…” [p. 19-20]
Dr. Verstraeten began his presentation by stating: “what I will present to you is the study that nobody thought we should do.” The study categorized the cumulative effect of thimerosal-containing vaccines administered to infants after one month of life and assessed the subsequent risk of degenerative and developmental neurologic disorders, and renal disorders before the age of six. Dr. Verstraeten stated that ALL of these relative risks were statistically significant.
And he noted that: “mercury at one month of age is not the same as mercury at three months, at 12 months, prenatal mercury, later mercury. There is a whole range of plausible outcomes from mercury.” When asked about the risk of aluminum, he stated: “the results were almost identical to ethylmercury because the amount of aluminum goes along almost exactly with the mercury one.”
Following the presentation, Dr. Roger Bernier (Associate Director for Science NIP) stated: “We have asked you to keep this information confidential….Consider this embargoed information.”[p. 113]
It is clear from the EIS transcript that the response to Dr. Verstraeten’s research findings differed between pediatricians, who were genuinely concerned about the hazards of both Thimerosal and aluminum, whereas officials of government and non-government organizations (NGOs, that are dependent on government and industry support, such as the World Health Organization), focused on the threat to vaccination policy and the risk of litigation were intent on burying the data and maintaining secrecy about the findings.
Pediatricians focused on the risks, public health: Dr. William Weil, represented the American Academy of Pediatricians (AAP) stated:
“moving from one month or one day of birth to six months of birth changes enormously the potential for toxicity. There are just a host of neurodevelopmental data that would suggest that we’ve got a serious problem. the potential for aluminum and central nervous system toxicity was established by dialysis data. To think there isn’t some possible problem here is unreal.”[p.24]
“Although the data presents a number of uncertainties, there is adequate consistency, biological plausibility, a lack of relationship with phenomenon not expected to be related, and a potential causal role that is as good as any other hypothesized etiology of explanation of the noted associations.
In addition, the possibility that the associations could be causal has major significance for public and professional acceptance of Thimerosal containing vaccines. I think that is a critical issue. Finally, lack of further study would be horrendous grist for the anti-vaccination bill. That’s why we need to go on, and urgently I would add.” [pg. 187 & 188]
“The number of dose related relationships are linear and statistically significant. You can play with this all you want. They are linear. They are statistically significant.” [p.207]
[Dr. Weil may well have been informed by the following research report: Aluminum Neurotoxicity in Preterm Infants Receiving Intravenous-Feeding Solutions in the NEJM(1997) whose authors concluded: “In preterm infants, prolonged intravenous feeding with solutions containing aluminum is associated with impaired neurologic development.” More on aluminum vaccine adjuvants below.]
Dr. Johnson: “This association leads me to favor a recommendation that infants up to two years old not be immunized with Thimerosal-containing vaccines if suitable alternative preparations are available… I do not want [my] grandson to get a Thimerosal containing vaccine until we know better what is going on.” [p. 198]
Dr. Robert Brent [a Scientific Adviser to an industry front-group] focused entirely on protecting corporations from lawsuits:
“The medical/legal findings in this study, causal or not, are horrendous and therefore, it is important that the suggested epidemiological, pharmacokinetic, and animal studies be performed. If an allegation was made that a child’s neurobehavioral findings were caused by Thimerosal containing vaccines, you could readily find junk scientist who would support the claim with “a reasonable degree of certainty”.
But you will not find a scientist with any integrity who would say the reverse with the data that is available. And that is true. So we are in a bad position from the standpoint of defending any lawsuits if they were initiated and I am concerned.” [pg. 229, emphasis added]
*[Dr. Brent was a member of the Board of Trustees of the American Council on Science and Health (ACSH) a food and chemical industry front group which the Center for Science in the Public Interest described as, “Voodoo Science, Twisted Consumerism”]
Dr. John Clements, who represented the WHO at the EIS conference, expressed alarm about the direction of the research, which he viewed as posing a threat to vaccination uptake if the information reaches the public:
“I am really concerned that we have taken off like a boat going down one arm of the mangrove swamp at high speed, when in fact there was not enough discussion really early on about which way the boat should go at all. And I really [don’t] want to risk offending everyone in the room by saying that perhaps this study should not have been done at all, because the outcome of it could have, to some extent, been predicted…, and we have all reached this point now where we are left hanging, even though I hear the majority of consultants say to the Board that they are not convinced there is a causality direct link between thimerosal and various neurological outcomes. I know how we handle it from here is extremely problematic.” [Emphasis added]
“…even if this committee decides that there is no association and that information gets out, the work that has been done and through the freedom of information that will be taken by others and will be used in ways beyond the control of this group. And I am very concerned about that as I suspect it already too late to do anything regardless of any professional body and what they say.”
“My mandate as I sit here in this group is to make sure at the end of the day that 100,000,000 are immunized with DTP, Hepatitis B and if possible Hib, this year, next year and for many years to come, and that will have to be with Thimerosal containing vaccines unless a miracle occurs and an alternative is found quickly and is tried and found to be safe. “ [emphasis added]
“I am very concerned that this has gotten this far, and that having got this far, how you present in a concerted voice the information to the ACIP [Advisory Committee on Immunization Practices] in a way they will be able to handle it and not get exposed to the traps which are out there in public relations.
My message would be that any other study, and I like the study that has just been described here very much. I think it makes a lot of sense, but it has to be thought through. What are the potential outcomes and how will you handle it? How will it be presented to a public and a media… I wonder how on earth you are going to handle it from here.“ [p. 247—249]
Other comments from those present include:
“We could exclude the lowest exposure children from the database”; “We could remove children that got the highest exposure levels since they represented an unusually high percentage of the [adverse] outcomes”; “We can push and pull this data any way we want to get the results we want;” “We could have predicted the outcomes.”
CDC’s Dr. Bernier reminded everyone: “consider this embargoed information…and very highly protected information.”
The concerns expressed at this Epidemic Intelligence Service meeting, by Dr. Clements and other public officials and industry representatives who asserted their determination to conceal the thimerosal evidence from the public, has been the policy of CDC and an international network. However, concealing the evidence does not eradicate the evidence. A compendium of 80 peer-reviewed, published studies found evidence of a link between thimerosal and neurological disorders, including autism. A recent Review paper (April 2017) documents that the continued use of thimerosal in underdeveloped countries provides evidence of its harmful impact.
WMP NOTE: This concludes Part One. Part Two of the Seven-Part series will be entitled: Public Trust of Government Pronouncements Regarding Vaccine Safety is Validated By Evidence of Deception and Corrupt Practices. Sharov’s Introduction outlines her well-researched and documented belief that, “Public health officials and the medical profession have abrogated their professional, public, and human responsibility, by failing to honestly examine the iatrogenic harm caused by expansive, indiscriminate, and increasingly aggressive vaccination policies.”
By Anna Von Reitz
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Many Lightworkers / Lightwarriors are being heavily psychically attacked since November of 2017 as stated in this article by Cobra.
Rozlyn and I make a compound called Orgonite which is made using equal parts of various metals and fiberglass epoxy resin. We add various crystals to each piece and this metal, resin, crystal combination works to help shield you, your property and loved ones from the brunt force of these attacks. We have a page here that explains how we place Orgonite (with images) on a property, around a house or apartment. Click here for more information about the Orgonite we make.
I’ve recently been guided to make Golden Section Pyramid frames using all wood pieces in their construction. The prototypes we have now work very well (almost instantly) to align and re-balance our energy (aura) grid and serve to bring us into a relaxed meditative state quickly.
I’m in process of finalizing the design to closely match the Alexander Golod Pyramids in Russia. When the design templates are available, I will update this post.
Thank you and kind regards,