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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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Big News: Costco To Become First Major Retailer To Stop Selling Roundup Herbicide?

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In Brief

  • The Facts:

    According to the non profit group Moms Across America, Costco is set to stop selling Roundup herbicide.

  • Reflect On:

    Despite the fact that harmful products continue to be approved across North America, the ultimate power to stop their use is us. When we become aware, we stop buying, and their profits drop. We are the ones that use it. Vote with your dollar.

It’s hard to even know where to start with the herbicide Roundup. Despite years of science exposing the inarguable health and environmental consequences of Roundup, federal health regulatory agencies in North America are still approving the herbicide, while multiple other countries have banned it and made its use illegal, citing various health and environmental concerns. Sri Lanka, for example, banned it five years ago due to its link to deadly kidney disease.

Furthermore, the countries approving it are doing so with massive amounts of corruption. These approvals come as a result of corrupt regulatory agencies here in Canada as well as the US, specifically the Food and Drug Administration (FDA) and the Centres for Disease Control and Prevention (CDC). The list of examples is very long when it comes to corruption and government connections to corporations like Monsanto, the corporation that created and sells Roundup. This is the only way these products get approved. It’s not science, it’s simply because of lobbying efforts and shady politics.

“It is commonly believed that Roundup is among the safest pesticides… Despite its reputation, Roundup was by far the most toxic among the herbicides and insecticides tested. This inconsistency between scientific fact and industrial claim may be attributed to huge economic interests, which have been found to falsify health risk assessments and delay health policy decisions.” – R. Mesnage (et al., Biomed Research International, Volume 2014 (2014), article ID 179691)

The latest approvals of glyphosate, the main active ingredient in Roundup, came from within Canada as well as Europe.

EU regulators recently decided to relicense glyphosate, a decision that was based on an assessment plagiarized from industry reports. It’s quite backwards that, for years, health regulators have been relying on the scientific reports from the companies that manufacture these products instead of seeking out independent scientific studies.

A group of MEPs decided to commission an investigation into claims that Germany’s Federal Institute for Risk Assessment (bFr) copy-and-pasted tracts from Monsanto studies. You can read more about that here.

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In addition, Monsanto colluded with the Environmental Protection Agency (EPA) to stifle cancer research that had any connection to their products.

The corruption is never-ending when it comes to the link between corporations and government agencies. In fact, only a few years ago, more than a dozen scientists from within the CDC put out an anonymous public statement detailing the influence corporations have on government policies. They were referred to as the Spider Papers.

Related CE Article: Robert F. Kennedy Jr. Explains How Big Pharma Completely Owns Congress

Costco

The corruption that plagues our federal regulatory agencies runs deep, and no matter how obvious the science becomes, like the dangers of Roundup, products that negatively impact our health seem to often get approved anyways. But something special on planet Earth is happening, and that’s massive awareness. We are finally starting to see through the veil that’s been blinding the masses in so many different areas within human life.

Sure, these products may continue to get approved, but we are the ones who are constantly choosing to do so. We don’t have to buy them, and that is why awareness is key.

Zen Honeycutt, the leader of Moms Across America, announced this week that Costco will not be selling the glyphosate-based weed killer Roundup Ready.

In a live video update posted on Facebook, Honeycutt stated that she received word that Costco was no longer selling Roundup or glyphosate-based herbicides.

While she’s allegedly not received any official word yet from Costco, she stated that she has talked to various people at the headquarters and regional offices confirming this news. This is huge news because, according to a 2015 article in National Geographic, Roundup is the second-best-selling herbicide in the U.S. for home lawn and garden use. Under a lucrative contract with Monsanto, Scotts Miracle-Gro owns the exclusive right to market Roundup in North America and much of Europe. Scotts distributes about $154 million worth (5.5 percent of the company’s total sales) of Roundup each year to retail giants including Amazon, Home Depot and Walmart.

So let’s hope it’s true.

I asked for an official statement and was told that usually, Costco does not issue press releases, etc discussing which items they have discontinued. Despite not hearing back from the Costco PR department, I decided to announce the information anyway. I told them that the 89,000 people who signed a petition to Costco, Home Depot, and Lowe’s deserved to have an answer. I knew that they would be happy to know that Costco was doing the right thing. – Honeycutt (source)

It’s weird how this is even a debate in some circles. This has been known for a very long time, and we’ve seen similar happenings with DDT in the past.

“Children today are sicker than they were a generation ago. From childhood cancers to autism, birth defects and asthma, a wide range of childhood diseases and disorders are on the rise. Our assessment of the latest science leaves little room for doubt; pesticides are one key driver of this sobering trend.” – October 2012 report by Pesticide Action Network North America (PANNA) (source)(source)

Glyphosate is really getting a bad name, as this new information regarding Costco is coming off the heels of some bad press for Monsanto (Bayer) as the case regarding school groundskeeper Dewayne Johnson was the first lawsuit claiming that glyphosate causes cancer to go to trial. There are thousands upon thousands of similar pending cases. Any jury that reviews all of the scientific evidence will not be able to rule in favor of Monsanto, and Johnson’s case was a great example that showed glyphosate caused his cancer.

The Takeaway

At the end of the day, it’s us who decide to use these products. Obviously, we’ve been misled and made to trust our federal regulatory agencies who are supposedly in charge of protecting us from these harmful products. It’s the complete opposite, and what these agencies do is actually quite criminal. This is why conscious media is so important. The same powers that control these corporations have a tight grip on mainstream media as well.

This is why this issue goes largely ignored, and the fact that so many people rely on mainstream media for information about what’s really happening in the world with regards to health, environment, finance, politics, etc. is why a lot of people are still completely unaware of important issues. This is also why governments have started a war on ‘fake news,’ which seems to be a cover for protecting corporate and government interests.

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New Study Links Acetaminophen (Tylenol) To Attention Deficit Disorder with Hyperactivity

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Another damning study indicates it is simply time to pull the plug on this outdated drug.

The study just published in JAMA Pediatrics once again indicated that women who take acetaminophen during pregnancy are more likely to have a child with attention deficit hyperactivity disorder (ADHD). The researchers also found that prenatal exposure to the medication was associated with a higher risk of having children who exhibit other emotional or behavioral symptoms.

Recent detailed analysis of clinical studies on acetaminophen (Tylenol) have concluded that this popular drug was ineffective for low back pain and provided no significant clinical relief of hip or knee osteoarthritis (OA) pain, while quadrupling the risk for liver damage.

All together, the results from all of these analyses further calls into question whether this drug should still be on the over-the-counter market or at all.

Background Data:

Acetaminophen is the only remaining member of the class of drugs known as “aniline analgesics” that is still on the market, as the rest were discontinued long ago. Acetaminophen only blocks the feelings of pain and reduces fever, it exerts no significant anti-inflammatory or therapeutic action.

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It is well-known that acetaminophen is very hard on the liver. About 40% of regular acetaminophen users show signs of liver damage. Acetaminophen reduces the liver’s store of the important detoxifying aid and antioxidant glutathione. When acetaminophen is combined with alcoholic drinks or other compounds toxic to the liver including other medications, its negative effects on the liver are multiplied. It should definitely not be used in anyone with impaired liver function and given the stress the liver experiences during pregnancy, it appears unwise to use it while carrying a child for both mother and the developing fetus.

Acetaminophen is often the drug of choice in children to relieve fever. However, use for fever in the first year of life is associated with an increase in the incidence of asthma and other allergic symptoms later in childhood. Asthma appears to be another disease process that is influenced greatly by antioxidant mechanisms. Acetaminophen severely depletes glutathione levels not only in the liver, but presumably other tissues as well, and should definitely not be used in people with asthma.

Each year acetaminophen causes over 100,000 calls to poison control centers; 50,000 emergency room visits, 26,000 hospitalizations, and more than 450 deaths from liver failure. In addition, regular use of acetaminophen is linked to a higher likelihood of Alzheimer’s disease, infertility, and hearing loss (especially in men under 50 years of age). Acetaminophen use during pregnancy has also been linked to the development of ADHD confirming animal studies showing acetaminophen use in pregnancy can disrupt normal brain development.

New Data:

To more closely assess the associations between maternal prenatal acetaminophen use and behavioral issues in their children, researchers in the United Kingdom collected and analyzed data 7,796 mothers along with their children. The data included acetaminophen use and behavioral assessments of the children were 7 years old. From this data the estimated risk ratios for behavioral problems in children after prenatal exposure to acetaminophen was determined.

The results showed that prenatal acetaminophen use at 18 and 32 weeks of pregnancy was associated with a 42% increased risk of the child having conduct problems and hyperactivity symptoms, while maternal acetaminophen use at 32 weeks was also associated with a 29% increased risk of the child having emotional symptoms and a 46% increase in total behavioral difficulties.

Obviously, the researchers concluded “Children exposed to acetaminophen prenatally are at increased risk of multiple behavioral difficulties, and the associations do not appear to be explained by unmeasured behavioral or social factors linked to acetaminophen use.”

Comment:

The results from this study and others are clear. Stay away from acetaminophen. Most people consider acetaminophen (e.g., Tylenol) as being an extremely safe pain reliever for both children and adults. The reality is that it can be extremely dangerous and causes significant side effects. The FDA has done a poor job alerting the public to the dangers of acetaminophen. In my opinion, it is a drug that serves no real medical purpose in the 21stcentury. Bottom line, it is time to pull it from the market.

As far as alternatives to acetaminophen during pregnancy, I would recommend ginger. Historically, the majority of complaints for which ginger (Zingiber officinale) was used concerned the gastrointestinal system as well as pain and inflammation. Several double-blind studies have shown ginger to yield positive results in a variety of gastrointestinal issues, especially those related to nausea and vomiting including severe morning sickness. In regards to pain and inflammation, dozens of clinical studies have supported this use with positive results in various forms of arthritis, chronic low back pain, muscle pain, and painful menstruation.

Ginger powder, ginger tea or a shot of fresh ginger juice added to any fresh fruit or vegetable juice is certainly a much better option to acetaminophen anytime, but especially during pregnancy.

My overall interpretation of the study is that depletion of glutathione caused by acetaminophen leaves cells, especially brain cells, susceptible to damage. I believe that future studies will not only show more evidence of a link to ADHD, but also autism as well. Glutathione is absolutely critical in protecting cellular function. Any factor that depletes glutathione is obviously going to alter proper development. In addition to acetaminophen, the following factors can deplete glutathione:

To boost your glutathione level it is important to focus on a diet rich in colorful fruits and vegetables. Their rich source of antioxidant phytochemicals and nutrients spare the use of glutathione and help to keep cellular levels high.

For additional related research use the following links: 


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Reference

Stergiakouli E, Thapar A, Smith GD. Association of Acetaminophen Use During Pregnancy with Behavioral Problems in Childhood. Evidence Against Confounding. JAMA Pediatrics. Published online August 15, 2016. doi:10.1001/jamapediatrics.2016.1775


Dr. Murray is one of the world’s leading authorities on natural medicine. He has published over 40 books featuring natural approaches to health. His research into the health benefits of proper nutrition is the foundation for a best-selling line of dietary supplements from Natural Factors, where he is Director of Product Development. He is a graduate, former faculty member, and serves on the Board of Regents of Bastyr University in Seattle, Washington. Please Click Here to receive a Free 5 Interview Collection from Dr Murray’s Natural Medicine Summit with the Top Leaders in the Field of Natural Medicine. Sign up for his newsletter and receive a free copy of his book on Stress, Anxiety and Insomnia.

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The Dangers of 5G to Children’s Health

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Mobile and wireless technologies are a ubiquitous feature of modern life. Most U.S. adults own smartphones, a growing proportion are “smartphone-only” Internet users and over a fourth report being online “almost constantly.” As for children, a 2014 survey of high-income nations reported that almost seven in ten children used a mobile phone, and two-thirds of those had a smartphone, usually by age 10. As described by Nielsen, it is now as common to see “a kid with a smartphone in their hand” as it was to see “a kid playing with a yo-yo in the years before the digital age.”

The enthusiasm with which the public has embraced each new mobile and wireless technology—most of which have never undergone any appropriate safety testing or standards development—suggests that consumers rarely stop to consider the health implications of the infrastructure shoring up their ability to browse, stream and download anytime and “on the go.” Consumers are not entirely to blame for their lack of awareness—it is not easy to disentangle the technologies’ health risks in the face of the telecommunications industry’s steady and calculated disinformation efforts and a captured Federal Communications Commission (FCC) that “follows the script of fabulously wealthy, bullying, billion-dollar beneficiaries of wireless.”

…powerful 5g (fifth generation) networks and technology are about to subject everyone, on a continuous basis, to unprecedented forms and amounts of mandatory irradiation – without prior study of the potential health impact or any assurance of safety

Now, however, a global 5G “frenzy” is upon us and is coming into full force. The rollout of “blazing fast” 5G technology will “dramatically increase the number of transmitters sending signals to cellphones and a host of new Internet-enabled devices.” The time is ripe for greater grassroots awareness of the undisclosed tradeoffs between convenience and 5G’s potentially catastrophic health effects. Far from a simple “next-gen” upgrade, powerful 5G (fifth-generation) networks and technology are about to subject everyone, on a continuous basis, to unprecedented forms and amounts of what retired U.S. government physicist Dr. Ronald Powell calls “mandatory irradiation”—without “prior study of the potential health impact” or any assurance of safety. Considering that young people (with their smaller body mass and developing brains) are particularly vulnerable to radiation, the Environmental Health Trust has termed 5G “the next great unknown experiment on our children”—and the entire human population.

Early warnings

In fact, the “giant uncontrolled experiment” on children and adults has already begun, despite an urgent international appeal by tens of thousands of scientists, doctors, environmental organizations and citizens calling for a halt to 5G deployment. In 2018, telecom carriers in the U.S. and Europe began rolling out 5G technology in dozens of cities. Focusing (for now) on “dense urban and high-traffic areas” in the U.S., AT&T began positioning its 5G infrastructure in major cities in eight states, and Verizon started offering 5G home broadband service in “select neighborhoods” in a handful of cities.

…health problems such as insomnia, miscarriage, memory problems and other neurological issues, and there are widespread reports of annihilation of insect and bird populations

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For the most part, health concerns have ranked as a tiny footnote in the midst of the massive hoopla about 5G’s speed and capacity, although trade magazines admit that there may be “some objections” to 5G due to “concerns over potential health risks.” In both Europe and the U.S., however, individuals living and working in proximity to newly installed 5G towers and antennas are telling a different story. Many have immediately started experiencing health problems such as insomnia, miscarriage, memory problems and other neurological issues, and there are widespread reports of annihilation of insect and bird populations.

In response to complaints from fire fighters subjected to 5G antennas, the International Association of Fire Fighters has gone on record as opposing “the use of fire stations as base stations for towers and/or antennas for the conduction of cell phone transmissions until a study with the highest scientific merit and integrity…is conducted and it is proven that such sitings are not hazardous to the health of our members.”

United Nations whistleblower recently drew attention to 5G’s dramatic impact on health in a widely circulated series of comments about 5G’s “seemingly overnight” rollout in Vienna, Austria. Describing 5G as a “silent war,” she commented:

“…Children are the most vulnerable to 5G depredation because of their little bodies. Friends and acquaintances and their children in Vienna are already reporting the classic symptoms of EMR [electromagnetic radiation] poisoning: nosebleeds, headaches, eye pains, chest pains, nausea, fatigue, vomiting, tinnitus, dizziness, flu-like symptoms, and cardiac pain. They also report a tight band around the head; pressure on the top of the head; short, stabbing pains around the body; and buzzing internal organs.”

Above and below

One of the novel dangers introduced by 5G technology is its reliance on high-frequency millimeter waves (MMWs), a bountiful and not previously commercialized portion of the electromagnetic spectrum. While 5G’s enthusiasts are quick to promise support for literally billions of devices, there is one catch—the shorter millimeter wavelengths cannot travel as far as the lower frequencies used for earlier generations of mobile technology. Thus, while there were about 300,000 wireless antennas on U.S. cell towers and buildings as of 2016 (a doubling since 2002), 5G will require “exponentially more”—millions of small cell towers every 500 feet “on every street corner.”

…Even in the home environment, 5G technology (will) blast through walls and cribs, making a mockery of the notion that ‘your home is your castle in which you are supposed to be safe

Organizations concerned about the health hazards of wireless radiation note that “Right now, you don’t have to live next to a cell tower….but once they have these [5G] cell antennas everywhere, you won’t be able to [move away].” Unfortunately, the “nowhere to hide” aspects of 5G are even more serious, because ground-based 5G systems will be supplemented by satellite-based systems. In March, 2018, the FCC approved the initial launch of over 4,400 low-Earth-orbit 5G communication satellites, to be followed by thousands more over the next two years—with the eventual result being 11 times more satellites orbiting the Earth than currently. The satellites will send “tightly focused beams of intense microwave radiation at each specific 5G device that is on the Earth,” while each device then sends “a beam of radiation back to the satellite.”

In practical terms, this means that in crowded locations such as airports, individuals’ bodies “will be penetrated by numerous beams of radiation as they walk or as other people walk around them with their 5G smartphones.” But even in the home environment, “5G technology [will] blast through walls and cribs,” making a mockery of “the notion that ‘your home is your castle’ in which you are supposed to be safe.”

More than skin-deep

Scientists, doctors and experts from around the world have issued repeated warnings about 5G’s risks, drawing on published research on MMWs as well as thousands of studies showing the harms caused by other mobile and wireless technologies.

In this context, industry and government claims that 5G technology is safe are completely disingenuous. In fact, the health effects of MMWs are already quite familiar to the U.S. military and defense agencies around the world. The U.S. has at its disposal non-lethal crowd control weapon systems (euphemistically named Active Denial Systems) that use millimeter waves to penetrate the skin of targeted individuals, “instantly producing an intolerable heating sensation that causes them to flee.” In research commissioned by the U.S. Army “to find out why people ran away when the beam touched them,” they discovered that targets “feel like [their] body is on fire.” Researchers also have warned that “the same parts of the human skin that allow us to sweat also respond to 5G radiation much like an antenna that can receive signals.”

Moratorium urgently needed

When the FCC endorsed the transition to 5G in 2016, then-Chairman Tom Wheeler (a former telecom industry lobbyist) vowed “to allow new [5G] technologies and innovations to evolve and flourish without needlessly prescriptive regulations.” Thus, even though 5G represented a radical shift in technology, the FCC proposed no further safety studies, instead continuing to rely on its “outdated, excessively permissive, and thus widely criticized, radiation-exposure guidelines that…are based primarily on a 30-year-old analysis…many years before the emergence of most of the digital wireless technology in use today.” A recent government study by the National Toxicology Program—which determined that cell phone radiation causes cancer—deemed the three-decade-old guidelines “unprotective.”

…children who began using either cordless or mobile phones regularly before age 20 had more than a fourfold increased brain tumour risk.

5G poses risks to all life on the planet—people, animals, insects and plants. However, it is clear that fetuses and children are among the most vulnerable members of the human population. Even prior to 5G, Swedish researchers concluded that “children are indeed more susceptible to the effects of EMF exposure at microwave frequencies” and reported that children who began using “either cordless or mobile phones regularly before age 20” had more than a fourfold increased brain tumor risk. Describing brain cancer as “the proverbial ‘tip of the iceberg,’” the researchers also observed that “no other environmental carcinogen has produced evidence of an increased risk in just one decade.”

The UN whistleblower states, “People’s first reaction to the idea that 5G may be an existential threat to all life on Earth is usually disbelief and/or cognitive dissonance. Once they examine the facts, however, their second reaction is often terror. We need to transcend this in order to see 5G as an opportunity to empower ourselves, take responsibility and take action.” Some of the actions that people have taken include signing the International Appeal; learning about the multiple reasons to be concerned about 5G radiation and telling others; talking to legislators about why rushing legislation that streamlines the deployment of 5G small cells is a bad idea (and also raising the awareness of legislators and state utility commissions about the risks of smart meters); and changing their relationship to their devices, including using wired rather than wireless Internet connections (or turning off WiFi routers at night) and adopting other simple steps.

5G promises to create an even “denser soup of electrosmog,” with incalculable health effects. In fact, any sane person who examines the evidence must concur with the authors and over 40,000 signatories of the International Appeal to Stop 5G on Earth and in Space, who agree that the rush to blanket the planet with 5G “constitutes an experiment on humanity and the environment that is defined as a crime under international law.”

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Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. CHD is planning many strategies, including legal, in an effort to defend the health of our children and obtain justice for those already injured. Your support is essential to CHD’s successful mission.

 

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