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The Vaccine Program: Betrayal of Public Trust & Institutional Corruption – Part 1 of 7

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Written by Vera Sharav

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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)]

Are children’s rights to a normal life being sacrificed as collateral damage to protect high utilization of vaccines?

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:

  • The American Academy of Pediatrics,
  • The Joint Committee on Vaccination and Immunization (JCVI, UK),
  • The World Health Organization,
  • WHO-Global Advisory Committee on Vaccine Safety (GACVS),
  • The European Medicines Agency (EMA),
  • The European Centre for Disease Prevention & Control (ECDPC),
  • The Brighton Collaboration and the Brighton Collaboration Foundation,
  • The Cochrane Collaboration,
  • The Institute of Medicine,
  • The Council for International Organizations of Medical Sciences (CIOMS),
  • The Global Alliance for Vaccines and Immunization (GAVI) which is bankrolled by the Bill and Melinda Gates Foundation,
  • World Bank and others.

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.]

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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);[1] additional CDC internal documents were obtained in July 2017.[2] 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).

Background:

What Did CDC Officials Know About Thimerosal; When Did They Know It, & What Did They Do About It?

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.”[4]

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.”[5]

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.” [6]

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.”[7]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.”[8]

The First Large-Scale Scientifically Sound CDC Epidemiological Study

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).[9]

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”[10]]

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.[11] 

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.” 

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Awareness

Scientist Replies To The Medical Industry’s False Claims About Aluminum Safety

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In Brief

  • The Facts:

    Aluminum.org is a pro-aluminum industry website. It even lists an Aluminum Caucus. This is a look into their list of “myths” about the safety of aluminum product they promote to see if their claims pass the proof-by-Pubmed test.

  • Reflect On:

    With all of the science clearly contradicting the medical and aluminum industry's claims of safety, how are they still able to approve the use of aluminum in our medications? It makes to sense, especially from a scientific standpoint.

By: James Lyons-Weiler, CEO/Director, The Institute for Pure and Applied KnowledgeCHD Contributing Writer

“Myth” #1: Exposure to aluminum causes Alzheimer’s Disease

Aluminum.org Claim: “Aluminum is not linked to Alzheimer’s disease, the cause (or causes) of which is unknown. In the words of the Alzheimer’s Association, ‘The research community is generally convinced that aluminum is not a key risk factor in developing Alzheimer’s disease.’

The World Health Organization has also concluded that “there is no evidence to support a primary causative role of aluminum in Alzheimer’s disease.’”

JLW’S ANALYSIS: It is highly odd to see the Alzheimer’s Association and the World Health Organization describing a type of consensus that there is no role for aluminum as a primary cause in Alzheimer’s disease for one simple fact: amyloid, the gunk that gums up the brain in Alzheimer’s dementia, is part aluminum. In fact, this has been known since 1985 [1].

…when the substance IS the condition, no level of epidemiological evidence will overrule the direct finding of the substance at the site of the disease manifestation.

So why and how could these organizations claim that aluminum does not play a primary causal role? The most likely explanation is the use of incorrect science and/or focus on the incorrect level of evidence. When a substance is co-localized to the site of condition, that’s pretty strong evidence that is play some role in the process – even if it is an inhibitory role, it’s still a role. But when the substance IS the condition, no level of epidemiological evidence will overrule the direct finding of the substance at the site of the disease manifestation.

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Examples include asbestos and various lung conditions. Asbestos fibres are extremely small; the most dangerous are <2 microns. When you breathe asbestos fibre in, the fibres remain in lung tissue for a long time and cause scarring and inflammation, leading to pleural plaques, widespread pleural thickening, pleural effusion, asbestosis, lung cancer, or mesothelioma [2].

Another example is the CDC’s use of the finding of the Zika virus in one brain of an aborted fetus with microcephaly to conclude that the Zika virus induces microcephaly. Dr. Anthony Fauci of US NIAID proclaimed that the finding was the “strongest evidence yet” that Zika was the cause of microcephaly in Brazil in 2015. However, oddly, although the incidence of Zika infection in Brazil increased with the mosquito season in 2016, there was no corresponding uptick in microcephaly– and no study was conducted to seek a role of the use of whole-cell pertussis vaccination in the slums of Northeast Brazil where the microcephaly outbreak peaked. So, evidence at multiple levels should be considered in the assessment of causality.

Amyloid is, of course, universally recognized as key deposit in the brain of people with Alzheimer’s disease. But what many people do not realize is that amyloid is produced in the bones, and as people age, their bone density reduces, and amyloid can be released. When it deposits in the brain, the compound (which is part aluminum), can lead to cerebral amyloid angiopathy, a condition in which blood vessels in the brain become coated and clogged with amyloid. This can lead to strokes and contributes to age-related dementia. So healthy bones are very important to reduce the amount of amyloid, and therefore aluminum, in the brain. Medium weight training is required as people age to keep bones strong.

The symptoms of severe acute aluminum exposure include cell death, meningitis, and dementia.

When aluminum itself enters the brain (and there is zero doubt that occurs [3-5]), it can have numerous effects. One, of course, is to serve as a building block by combining with amyloid precursor protein. Aluminum can also have nefarious influences on a brain cell’s ability to fold proteins properly, lead to disease condition in which cellular necrosis (seepage of oddly, improperly shaped proteins) can occur, wreaking havoc with intercellular signaling. The inflammasome can be activated, leading to the recruitment of intrinsic immunity cellular responses (including microglial activation[6]). It causes the release of cytokines, especially IL-6, which make the brain’s innate immune cells act as if nearby cells are under viral attack. The symptoms of severe acute aluminum exposure include cell death, meningitis, and dementia. Vaccine Papers has a good resource for studies on the effects of various forms of aluminum [7].

“Myth” #2: Aluminum present as an active ingredient in some antiperspirants leads to breast cancer.

Aluminum.org Claim: “Aluminum is not, nor has it ever been, classified as a carcinogen. Further, there is no convincing scientific evidence that aluminum-based antiperspirant use contributes to the development of breast cancer. Less than 0.02% of aluminum in contact with skin is taken up by the body, the rest being excreted in a very short time.”

“The American Cancer Society states “There are no strong epidemiologic studies in the medical literature that link breast cancer risk and antiperspirant use, and very little scientific evidence to support this claim. In fact, a carefully designed epidemiologic study of this issue published in 2002 compared 813 women with breast cancer and 793 women without the disease. The researchers found no link between breast cancer risk and antiperspirant use, deodorant use, or underarm shaving.’”

JLW ANALYSIS: study by Linhart et al. (2017)[8] found that the use of aluminum-containing deodorant increased both aluminum content in breast tissue and breast cancer risk, confirming studies from as early as 2003 (McGrath 2003) [9]. A growing number of studies show that mammary epithelial cells cultured accumulate mutations when exposed to aluminum [10]. While the epidemiological literature is divided, it is surprising to see Aluminum.org provide only the single study that found no link, while two other studies, including one that pre-dated the study they did cite, do report increased tissue burden and increased risk of breast cancer.

Aluminum is becoming so ubiquitous that single source safety considerations are now obsolete.

“Myth” #3: Consuming aluminum in antacid pills can cause health problems.

Aluminum.org Claim: “Aluminum is poorly absorbed by the body. This means that most (at least 99.9%) of aluminum ingested from food and water merely passes through the digestive tract and out of the body. Several studies have found no adverse effects for those who have ingested even large quantities of aluminum-containing antacids from antacids…

Additional reassurance regarding aluminum’s safety can be derived from the fact that frequent users of oral antacids may consume very high quantities of aluminum (e.g. up to 1000 mg/day), several orders of magnitude higher than the intake from ordinary food and water intake, yet no adverse health effects have been demonstrated…

The Center for Disease Control’s Agency for Toxic Substance & Disease Registry notes, ‘An extremely small amount of the aluminum found in antacids [is] absorbed [through ingestion].’ And further, ‘The FDA has determined that aluminum used as food additives and medicinals such as antacids are generally safe.’”

JLW Analysis: Now this is interesting, because Paul Offit of Children’s Hospital says that we get “far more” aluminum from diet than from vaccines. But we will come back that.

Aluminum.org is correct to say we absorb a tiny fraction of the aluminum we ingest. However, any dietary aluminum from one source has a cumulative effect from dietary aluminum from any other source. So, for example, cooking rhubarb in aluminum foil will lead to very high levels of ingested aluminum. Following that up with an antacid that contains aluminum adds to the total. Taking pills that contain aluminum in a carrier base also increases the dose. And then taking aluminum-containing vaccines at the same time increases the total aluminum compound dose even further. Aluminum is becoming so ubiquitous that single source safety considerations are now obsolete.

For a given day, a one-time exposure is probably not a concern for 130-lb woman or 1 180 lb-man. But in children, it’s a different story. Why? Body weight determines the toxicity of a dose. And while ATSDR looked at the effects of dietary aluminum, it is incorrect to say that studies found no ill effects. One key study (Golub et al., 1989) [11] in fact did report food intake problems (cyclic food intake, indicative of exposure to a toxin, or poison), in spite of being represented by the FDA as not finding any adverse reactions. Numerous other studies also showed that dietary forms of aluminum have adverse events (see accumulated list [12]).

The primary concern over aluminum toxicity are its whole-body accumulation, and its synergistic effect on the toxicity of other toxic chemicals in our environment – such as fluoride. A study by Kaur et al. in 2009 [13] found alterations in the neurotransmitters (e.g., dopamine, norepinephrine, and serotonin) due to fluoride in rats, and that the changes were more pronounced in animals given fluoride and aluminum together. They reported that histological evidence showed “deprivation of neuronal integrity with higher magnitude in concurrent fluoride and aluminum exposure, as compared to fluoride alone” and they concluded that aluminum appears to enhance the neurotoxic hazards caused by fluoride.

“Myth” #4: It is dangerous to cook with aluminum pots and pans.

Aluminum.org Claim: “The Food and Drug Administration studied this issue in the early 1980s and reported no safety concerns from using aluminum cookware. More recently, the Center for Disease Control’s Agency for Toxic Substance & Disease Registry reported that ‘foods cooked in aluminum pots are generally considered to be safe.’

An independent study by America’s Test Kitchen in 2012 found that “In lab tests … tomato sauce … cooked in an aluminum pot for two hours and then stored in the same pot overnight was found to contain only .0024 milligrams of aluminum per cup.” For the sake of comparison, according to the FDA, ‘the daily aluminum intake for man from all dietary sources can range from 10 to 100 mg per day.’ Consumption at this level is considered safe.”

JLW Analysis: The category “GRAS” is an archaic category based on no science, but rather a general assumption of safety applied to food additives based on information available prior to the 1960s (and before). As we know, we are living in an increasingly toxic environment; we do not live on our grandparent’s planet. But even absent concern with low doses of aluminum from pots and pans, any amount is cumulative to aluminum from other exposures. Since there are alternative materials, why take on further risk given that aluminum is becoming so ubiquitous?

Offspring showed growth retardation and somewhat delayed neurobehavioural development, which was consistent with maternal toxicity…

“Myth” #5: The aluminum salts used to clean municipal drinking water pose a danger to human health.

Aluminum.org Claim: “Virtually every municipal water purification system in the world uses aluminum salts to remove impurities and provide safe, healthy and accessible drinking water. The global public health benefits enabled by these systems are numerous and have prevented innumerable water-borne diseases.

Health Canada spent 10 years and millions of dollars studying this issue and concluded: ‘There is no consistent, convincing evidence that aluminum in drinking water causes adverse health effects in humans, and aluminum does not affect the acceptance of drinking water by consumers or interfere with practices for supplying good water.’”

JLW Analysis: Here we have a clearly misleading effort to cherry-pick not just from the scientific literature. The same report cited by Aluminum.org also reported:

An increase in pre-weaning mortality and a delay in weight gain and neuromotor development in surviving pups were reported in the offspring of albino Wistar rats given oral doses (in the diet) of aluminum chloride (equivalent to about 155 and 192 mg Al/kg bw per day) from day 8 of gestation through parturition… Neurotoxicity and weight loss were also reported in mouse dams fed a diet containing aluminum lactate at 500 or 1000 ppm from day 0 of gestation to day 21 postpartum.

Offspring showed growth retardation and somewhat delayed neurobehavioural development, which was consistent with maternal toxicity…

In a study in which pregnant rats were exposed to a 20% solution of Maalox (a stomach antacid) in tap water (approximately 3.2 mg Al/mL) from the second day of gestation, Anderson et al.205 found that offspring of aluminum-exposed dams showed significantly more aggressive responses, although the time spent on each aggressive response was less than in controls. Furthermore, the offspring of aluminum-exposed mothers showed a significantly longer latency period in the escape-training phase following a three-day period of exposure to non-avoidable shocks.

The report cited by Aluminum.org also included:

Several epidemiological studies have reported a small increased relative risk of AD associated with high aluminum concentrations in drinking water… All these studies have methodological weaknesses, but a true association between high aluminum concentrations in drinking water and dementia (including AD) cannot be ruled out, especially for the most elderly (e.g., over 75)…

According to a review by Doll… the evidence from several epidemiological, clinical and experimental studies suggests that aluminum is neurotoxic in humans but does not suggest that it causes AD. However, Doll… stressed that the possibility that aluminum does cause AD must be kept open until the uncertainty about the neuropathological evidence is resolved.

Aluminum in water can easily be avoided by consuming silica-rich mineral water, which is purported to help reduce total body burden of aluminum [14]

On Day 1 of life, infants receive 17 times more aluminum than would be allowed if doses were adjusted per body weight.

“Myth” #6: Aluminum contained in certain vaccines make them unsafe.

Aluminum.org Claim: “Aluminum salts have been used to improve the immune system’s response to vaccines for more than 70 years. Most of the small amount of aluminum used in the vaccinations is quickly expelled by the body. About half of the aluminum is gone in 24 hours; three-quarters is eliminated in two weeks and virtually all of it disappears within three years.”

“There are recent reports of a neurologic disease called macrophagic myofasciitis (MMF) suspected to be caused by injections of aluminum-containing vaccines. The role of aluminum in the mechanism of this disorder is unclear. The only known undesirable effects that are attributable directly to aluminium salts contained in vaccines are possible local inflammatory reactions, which in some cases are due to the speed of the injection of the vaccine or to insufficient agitation of the vial.”

“In 2008, the World Health Organization’s Global Advisory Committee on Vaccine Safety (GACVS) stated: “From the most recent evidence, there is no reason to conclude that a health risk exists as a result of administration of aluminium-containing vaccines. Neither is there any good scientific or clinical basis for recommending any change in vaccination practice.”

The Centers for Disease Control and Prevention has concluded that the use of aluminum in vaccines is safe.”

JLW Analysis: Here we see the same abuse of logic that was used to argue that ethyl mercury from vaccines cleared quickly: the “gone” that Aluminum.org is referencing here are serum levels; there are precious few studies that examine whole-body elimination rates but Flarend et al. [15] found only 4.6% of aluminum left the body of rabbits after 28 days.

Calculations of the “safe” levels of aluminum by Mitkus et al. (the US FDA) [16] were based on myriad flawed assumptions, most importantly the use of dietary aluminum vs. injected vaccine forms of aluminum, on adult mice (instead of infant mice) to assess the safety of aluminum for use as injected forms in infant humans. But even then, we now know that their actual calculations were flawed exercises in a shell game: divide doses into three body compartments, use serum clearance rather than whole body clearance, and divide exposure by 365 days… and then the numbers look safe. We don’t need the numbers to just look safe. We need to know the safe levels of doses of injectable forms of aluminum using dose escalation studies. This was the conclusion of an extensive and careful IPAK analysis [17] which found these and other flaws and concluded that:

“On Day 1 of life, infants receive 17 times more aluminum than would be allowed if doses were adjusted per body weight.”

Regarding aluminum from vaccines and diet, Children’s Hospital in Philadelphia offers health care consumers a video on the webpage featuring Dr. Paul Offit, a CHOP employee claiming (quite incorrectly for infants up to six months of age) that we get far more aluminum from food and water, and anything made of water, than we would ever get from vaccines.

Again, IPAK’s analysis shows, considering body weight, that the information published on the CHOP website is incorrect, and, like Aluminum.org, is misleading consumers into a false sense of safety. This finding is consistent with that of Dorea and Marques [18].

IPAK Calculated Accumulations of Aluminum in Humans by Source. See report [19] for details and additional results. (mcg/kg = micrograms per kilogram cumulative body burden.)

Parents are being tricked by the CHOP website into bringing their infants to be exposed – repeatedly – to acute toxic doses of injected aluminum to accept a medical procedure and pharmaceutical product that is only assumed to be safe – not shown to be safe by science.

Studies now exist that show that aluminum is found in the brains of people with Alzheimer’s, autism, multiple sclerosis, Parkinson’s disease – and studies exist that show that safe removal of aluminum via chelation is effective in reducing the symptoms of these and other conditions (19). The consumption of silica-rich mineral waters was found to increase urinary excretion of aluminum from patients with Secondary Progressive Multiple Sclerosis (SPMS) (20).  Reversal of a disease by removing a factor proves that factor is a key cause.

Therefore, I believe that both CHOP and Aluminum.org are committing fraudulent false advertising, and one or more class action suits against both should be taken up as soon as possible. The Aluminum.org webpage and the CHOP video spreading false and misleading information on aluminum safety must come down.

Citations

  1. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC554575/
  2. https://www.atsdr.cdc.gov/csem/csem.asp?csem=29&po=9
  3. https://www.ncbi.nlm.nih.gov/pubmed/28159219
  4. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784951/
  5. https://www.sciencedirect.com/science/article/pii/S0946672X17308763
  6. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784951/
  7. http://vaccinepapers.org/aluminum-inflammation-interleukin-6/
  8. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514401/
  9. https://www.ncbi.nlm.nih.gov/pubmed/14639125
  10. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552203/
  11. https://www.ncbi.nlm.nih.gov/pubmed/2755419
  12. http://vaccinepapers.org/the-foundation-for-al-adjuvant-safety-is-false/
  13. https://www.ncbi.nlm.nih.gov/m/pubmed/19538017
  14. https://www.hippocraticpost.com/nursing/why-everyone-should-drink-silicon-rich-mineral-water/
  15. https://www.ncbi.nlm.nih.gov/pubmed/9302736
  16. https://www.ncbi.nlm.nih.gov/pubmed/22001122
  17. https://www.sciencedirect.com/science/article/pii/S0946672X17300950
  18. https://www.ncbi.nlm.nih.gov/pubmed/20010978
  19. http://ipaknowledge.org/resources/IPAK_Aluminum_Flyer.pdf
  20. https://www.ncbi.nlm.nih.gov/pubmed/29128442
  21. https://www.hindawi.com/journals/bmri/2014/758323/

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The Shocking Lack of Evidence Supporting Flu Vaccines

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In Brief

  • The Facts:

    Multiple reasons exist explaining why it makes more sense not to receive the flu vaccine. It makes more sense to focus on a strong and healthy immune system to combat the flu, yet the vaccine is heavily marketed every single year.

  • Reflect On:

    With so many concerns being raised every single year regarding the flu shot, why does the corporation still blast out mass marketing, propaganda false information and fear?

This article was written by Sayer Ji, Founder of Greenmedinfo.com. His work is reproduced and distributed here with the permission. Want to learn more from GreenMedInfo? Sign up for the newsletter here: http://www.greenmedinfo.com/greenmed/newsletter.”

As it presently stands, it is not sound medical science, but primarily economic and political motivations which generate the immense pressure behind mass participation in the annual ritual of flu vaccination.

It is a heavily guarded secret within the medical establishment (especially within the corridors of the CDC) that the Cochrane Database Review (CDR), considered by many within the evidence-based medical model to be the gold standard for assessing the therapeutic value of common medical interventions, does not lend unequivocal scientific support to the belief and/or outright propaganda that flu vaccines are ‘safe and effective.’ao-opts a natural process, generating a broad range of adverse unintended consequences, many of which have been documented here. Vaccine proponents would have us believe that natural immunity is inferior to synthetic immunity, and should be replaced by the latter (see our article on the vaccine agenda: Transhumanism/Dehumanism).  In some cases they even suggest breastfeeding should be delayed during immunizations because it “interferes” with the vaccine efficacy.

This warped perspective follows from the disingenuous standard vaccine researchers use to “prove” the “efficacy” of their vaccines. The chemical kitchen sink is thrown at the immune system in order to conserve the expensive-to-produce antigen and to generate a more intense immune response – a process, not unlike what happens when you kick a beehive. These chemicals include detergents, anti-freeze, heavy metals, xenotrophic retroviruses, DNA from aborted human fetuses (diploid cells) and other species, etc. Amazingly, vaccine researchers and manufacturers do not have to prove the antibodies actually have affinity with the antigens they are marketed to protect us against, i.e. they do not have to prove real world “effectiveness,” only a surrogate marker of “efficacy.”  Yet, recent research indicates in some cases no antibodies are required for immunity against some viruses, running diametrically opposed to the orthodox tenets of classical vaccinology.

Another point that can not be understated is that the trivalent (3-strain) influenza vaccines are incapable of protecting us against the wide range of pathogens which produce influenza-like illness:

“Over 200 viruses cause influenza and influenza-like illness which produce the same symptoms (fever, headache, aches and pains, cough and runny noses). Without laboratory tests, doctors cannot tell the two illnesses apart. Both last for days and rarely lead to death or serious illness. At best, vaccines might be effective against only Influenza A and B, which represent about 10% of all circulating viruses.” (Source: Cochrane Summaries).

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It is therefore exceedingly clear that it is a mathematical impossibility for influenza vaccines to be effective at preventing wild-circulating strains of influenza. Support of the immune system, then, becomes the most logical and reasonable solution.

Immune Status Determines Susceptibility To Infection

The fact is that our immune status determines susceptibility. If the immune system is continually challenged with environmental toxicants, nutritional deficiencies and/or incompatibilities, chronic stress, influenza is far more likely to take hold. If your immune system is strong, many infectious challenges occur, are met with an appropriate response, and often go unnoticed. In other words, it is not a lack of a vaccination that causes infection, rather, the inability of the immune system to function effectively. [Note: In some cases, we may become infected and the ultimate outcome is that we enjoy even greater immunity.]

Moreover, there is an ever-growing appreciation within the scientific community that influenza cannot be defined as a completely exterior vector of morbidity and mortality, as portrayed within the mainstream, but is actually comprised of many proteins and lipids derived from the host it occupies, and may even be more accurately described as a hijacked cellular microvesicle (exosome), i.e. it’s as much us as other.

Learn more by reading our recent articles on the topic, “Why The Only Thing Influenza May Kill Is Germ Theory,” and “Profound Implications of the Virome for Human Health and Autoimmunity,”and by watching the incredibly eye-opening NIH lecture by Dr. Herbert Virgin below on the virome and the potentially indispensable role that viruses play in establishing the baseline genotype-phenotype relationship within the human immune system:

Additionally, while there are a broad spectrum of natural substances which have been studied for their anti-influenza properties, vitamin D deserves special consideration due to the fact that it is indispensable to produce antiviral peptides (e.g. cathelicidin) within the immune system, and can be supported for pennies a day.

For instance, a study published in the American Journal of Clinical Nutrition in 2010, revealed that children receiving 1200 IUs of vitamin D a day were at 59% reduced risk for contracting seasonal Influenza A infection. Moreover as a secondary outcome, only 2 children in the treatment group versus 12 for the control group, experienced an asthma attack. For more information on Vitamin D and immunity, visit the amazing research resource on the topic: VitaminDWiki.com.

Other preventive strategies that are evidence-based, and are available without a prescription include:

1) Echinacea Tea: J Altern Complement Med. 2000 Aug;6(4):327-34

2) Elderberry:  J Altern Complement Med. 1995 Winter;1(4):361-9.

3) American Ginseng:  J Altern Complement Med.  2006 Mar;12(2):153-7.

4) Green Tea: J Nutr. 2011 Oct ;141(10):1862-70. Epub   2011 Aug 10.

5) Probiotics: Pediatrics. 2009 Aug;124(2):e172-9.

6) Vitamin D: PLoS One. 2010;5(6):e11088. Epub 2010 Jun 14.

Learn more by visiting our Anti-Influenza Research Portal.

Sayer Ji is founder of Greenmedinfo.com, a reviewer at the International Journal of Human Nutrition and Functional Medicine, Co-founder and CEO of Systome Biomed, Vice Chairman of the Board of the National Health Federation, Steering Committee Member of the Global Non-GMO Foundation.

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Author Of “How To End The Autism Epidemic” Reveals A Deep Truth About Autism

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In Brief

  • The Facts:

    Author, JB Handley has published a book regarding the link between vaccines and autism. It's full of information that's never acknowledged, presented or even known about by most Doctors.

  • Reflect On:

    With so many examples, lawsuits, and scientific evidence, not to mention hundreds of scientists and doctors speaking out, why is there never a platform generated for an open discussion between experts in the field? Why is one side always ridiculed?

Discussing vaccines and autism isn’t an explosive topic, it’s thermonuclear. Both sides of the argument feel, with great passion, that the health and welfare of children is at stake. Much of that passion is the product of several lies told repeatedly. These lies form a foundation for self-interested parties to deny, obscure, and misdirect the truth about what’s happening to millions of children. They pit well-meaning parents against well-meaning parents. Remove the lies and you’re left with a deeply disturbing explanation for why so many children seemingly have autism out of the blue.  JB Handley – Author of How To End The Autism Epidemic 

How To End the Autism Epidemic – with many people saying is the best book on the link between vaccines and autism – is already an Amazon best seller (it hit the list even before it was released) and has recently been sent to all of the senators in Washington.

Author, JB Handley, whose own son Jamieson, showed warning signs that very night after receiving his 6 vaccines given at his ‘well baby’ appointment at two months of age.  Handley shares that something was clearly very wrong after that visit to the trusted family paediatrician, and his once perfectly healthy baby quickly morphed into a very sickly child.

Jamieson quickly regressed into autism and was often in constant pain with severe gut issues, his future now ruined.  This tragedy, that has also become millions of other parent’s far too eerily similar nightmare, propelled Handley on a journey that has become his life’s mission and purpose. Nothing fuels a parents fire to do something, more than that of their own child’s suffering.  It also is the reason why parents of other injured children won’t go away, until something is done about this crippling crisis.

JB, who studied at the prestigious Stanford University, has a very sharp grasp and innate ability to interpret and convey science, which is truly impressive. The research gone into this book is meticulous.

The book is written in a way that is concise and incredibly compelling, but most importantly, it is easy to understand.  This is a very important factor when discussing vaccine topics, simply because much of the ‘vaccine science’  in the last few decades has been manipulated, and you usually need a very sharp mind to see how this has happened.

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The way studies are written actually go over most people’s heads, and this is why most don’t look at the studies themselves in detail, for they simply do not understand what things mean, or how to question the data presented, let alone to see how the statistics were manipulated.

The book enables the reader to clearly see inside popular studies which are repeatedly shared in the public to shut down further discussion on issues surrounding vaccine safety and efficacy.

Whilst JB writes only briefly on his own families experience with autism, the book relies mostly on information from science, emails from FOIA requests, court transcripts, and expert testimonials and shares some truly shocking things.  I won’t go into all of them here of course, but there is one testimony from a court case with a leading ‘vaccine expert’ Dr. Stanley Plotkin, that you should be aware of – so that it encourages you to question the ethics of the entire industry – and to purchase the book to find out what other bombshells it contains.

Whilst denying it at first, when questioned by Lawyer Mr. Siri, Dr. Plotkin admitted that he had conducted experimental vaccine tests on mentally disabled subjects (both adults and children), as well as babies born to mothers in jail.  Testing on the most vulnerable of people means that you can conduct studies where the results can easily be manipulated (for example, you won’t have to say in the study that vaccines cause mental illness if a test subject already is mentally ill).

This is highly disturbing to say the very least, but these sorts of ethics are not at all rare in the vaccine industry.

The book also exposes financial interests that many of the well-known vaccine proponents such as Dr. Paul Offit, Dr. Peter Hotez, Dr. Eric Fombonne and Dr. Paul Shattuck have.  Combined it’s many tens of millions.  It’s easy to see why they are used publicly (and so often)  to provide ‘expert commentary’ that vaccines are safe and effective.

For decades, the concern regarding vaccine ingredients was mainly around the neuro-toxic thimerosal, in recent years, there has been a switch to focus on aluminum, an adjuvant found in many of today’s vaccines at alarmingly high amounts. JB has written extensively about this in articles and information is also found in his book.

One expert who has been studying aluminum for decades is that of Professor Chris Exley who had this to say about JB’s book

I have been thinking about the toxicity of aluminum for thirty-five years. It is my life’s work. Before we completed our recent research on aluminum in brain tissue in autism, I could not see a direct link between human exposure to aluminum and autism. I certainly saw no immediate role for aluminum adjuvants in vaccines in autism. The missing link was a mechanism whereby the brain would be subjected to an acute exposure to aluminum, for example, as occurs in aluminum-induced dialysis encephalopathy. Pro-inflammatory cells, some originating from blood and lymph, heavily loaded with a cargo of aluminum in brain tissue in autism provided that missing link. We all tolerate the toxicity of aluminum adjuvants in vaccines. Unfortunately, some of us are predisposed to suffer, as opposed to tolerate, the toxicity of aluminum adjuvants, and this may cause autism.

Autism is a disease, and it is not inevitable. J.B. Handley’s elegant synthesis of what we know and what we need to know argues that autism could and should be preventable. I agree with him.―Professor Christopher Exley, PhD, fellow, Royal Society of Biology; professor of bioinorganic chemistry, Keele University

Like it or not, the subject of whether or not ‘vaccines cause autism’ is one that won’t go away, and if anything, becomes talked about more each day, simply because so many parents are sharing that they too, saw something happen to their own children that they can only put down to recent vaccines.

The Implications of Truth

Despite what we are told by the mainstream media and medical industry when it comes to vaccines causing autism, the science here isn’t anywhere near settled.  Some of you might perhaps realize this ‘parroted’ term is perhaps repeated on purpose, it’s used to ‘shut down’ further discussions.  And this should make you question why?  Why are we not able to ask important questions, regarding safety, ingredients and studies?  What other drugs, that you know of, are we not allowed to question?  Could it be down to money?

Imagine if it did come out that vaccines triggered autism in children.  Wouldn’t there be a tidal wave of court cases with hundreds of thousands of claimants wanting compensation?  I wonder how much money this would amount to? The US Government has already paid out close to US 4 Billion (with taxpayers money) and that is for vaccine injury, not for Autism claims.

It is already estimated that for the cost for caring for people with autism will surpass $1 trillion in 2025, and this figure is nothing to do with compensation.  It is a frightening future that we have and one that is headed our way very soon.

The Science is Not Settled…

Science is never settled because it is a field that should always be encouraging further research and critical questioning.  Science has become so corrupted over the last few decades that it is actually an area that should now perhaps raise suspicion, especially where big profits are involved, and especially if the companies who produce the products aren’t held responsible financially if something goes wrong.

Vaccines, unlike drugs, are protected by a 1986 law that gives protection to all vaccine manufacturers. They cannot be sued.  This is disturbing to most people when they discover this, and with very good reason.  Without liability, why would a company bother to change how something is made, to improve it, if no one is going to come knocking on your door demanding change and making you pay anyone that sues you for damage? It’s called the National Childhood Vaccine Injury Act.

It is particularly intriguing to see that vaccine research is an area that vaccine manufacturers and those that speak for them, staunchly seem to not want this to be looked into further – especially around the issue of vaccine safety, and it’s connection to autism.

Vaccines have not been tested adequately in relation to them increasing the rates of autism, you might be shocked to know that only one, the MMR  (and also only one ingredient, Thimerosal) has been studied by the CDC – with questionable results at that.  They never mention these other studies on Thimerosal toxicity or acknowledge the comments made by their longtime scientist Dr. William Thomspon, who blew the whistle on the MMR vaccine.

Thompson bravely told the world that it was “the lowest point” in his career that he “went along with that paper.” He said that the authors “didn’t report significant findings” and that he is “completely ashamed” of what he did, that he was “complicit and went along with this, and that he regrets that he has “been part of the problem.” (source)(source)(source)

Vaccines contain so many different ingredients and to have just studied one, seems beyond incredulous. With over 20 different types of vaccines (some which have multiple diseases in them) this is terrible ‘evidence’ that vaccines don’t cause autism.  The CDC (which, unbeknownst to the average person, actually owns 20 vaccine patents) cannot state that is true, because they have simply, not studied them all.

So the science here is most certainly not at all ‘settled.’

What does the US vaccine court say about vaccines causing autism?

Inside JB’s book is a chapter titled ‘The clear legal basis that vaccine’s cause autism’ is dedicated to how the vaccine court operates, and where it was admitted that a child’s injury, and subsequent diagnosis of autism, was because of a vaccine.  One case, which was leaked to the public, regarding Hannah Polling, whose family was given $20 million in compensation, under the condition they never speak out about the finding.  For those that want to deny there is a connection between vaccines and autism, this is a chapter they will have real trouble refuting.

Autism is predicted to affect a whopping 1 in 2 children by the year 2025. Yet nothing seems to be being done by the medical industry about the ’cause’, and certainly nothing effective for its treatment.  Many families are suffering in silence and are becoming impoverished looking after their sick children.

For those in countries like Australia and the UK, where people rely on the socialized ‘free’ health care system, many children are not being given the testing and the treatments that they need. Whilst genes are typically blamed for autism, yet there is no definitive gene for autism.  The money being put into autism research is just not going into the right areas, that would make a huge positive difference.  If it was, the autism rates would be going down.

I feel this is important to note, that the book is not about making the author money to line his pockets. 100% of the profits from How To End The Autism Epidemic are all being donated to several organizations, to help families dealing with autism.

We could do something about autism, and we could do it quickly if our Governments paid attention. The answers are found in this book.

If you are concerned about this issue, want solid science and to want to know the truth about how the vaccine industry operates, this book is for you.

To purchase the book in either paper back of kindle, please click here Remember, the proceeds go to helping other families dealing with autism.

Below is an interview with the author JB Handley

.

Vaccine Court has paid 3.7 billion in damages to families

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