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Fast-Tracking Mandatory Vaccination While Government & Media Muzzle Scientists

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Turning their backs on the human rights principle of voluntary informed consent memorialized in the Nuremberg Code after World War II, health authorities in France and Italy are fast-tracking involuntary vaccine mandates for school-age children. In Italy, millions of Italians have been demonstrating since June, protesting the infringements to parental rights. On July 28, industry-beholden Italian legislators voted 296-92 to pass a one-size-fits-all law that mandates multiple doses of ten vaccines for preschoolers through teenagers, imposing steep fines for parents who do not comply. Mainstream media outlets in both Italy and the US ignored the record protests against medical coercion.

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Vaccines are big business, and the new vaccine mandate ensures the continued flow of profits to the $32 billion industry despite steady erosion of public confidence in vaccine safety.

Why Italy? And why now? Italy’s pharmaceutical sector is one of the largest in the world. Vaccines are big business, and the new vaccine mandate ensures the continued flow of profits to the $32 billion industry despite steady erosion of public confidence in vaccine safety. A recent survey found widespread doubts among Italian and French citizens about the importance and safety of vaccines. A cascade of recent scientific studies have described the emergence of new vaccine-related autoimmune illnesses and the inferior health status of vaccinated compared to unvaccinated children. Furthermore, a slate of films, news reports and government investigations have exposed widespread corruption among vaccine regulators, government efforts to hide serious vaccine-related adverse reactions and intimidation of scientists who publish data contrary to the orthodoxy that all vaccines are always safe for all children.

Kill the Messenger

One important study, published in early 2017 in the International Journal of Vaccines and Vaccinationby two highly regarded Italian scientists, raises alarming new questions about quality control by vaccine manufacturers with implications for the vaccine safety debate. (The World Mercury Project previously summarized the study here.) Coauthored by physicist Antonietta Gatti and pharmacist Stefano Montanari, the study uncovered the nearly universal presence in vaccines of “micro-, sub-micro- and nanosized inorganic foreign bodies” and “debris”—ingredients not declared in the package inserts.

In every human vaccine, Gatti and Montanari found wide-ranging contamination, including minute particles of lead or stainless steel in all of the vaccine samples analyzed; chromium in over half (25/44); tungsten in almost a fifth (8/44); and many other varieties of metallic particles.

In a reasonable world, the startling finding that vaccines are widely contaminated with heavy metal particulates would be front-page news, and the two researchers who discovered the contamination would be hailed as diligent scientists dedicated to improving vaccine safety. Instead, Drs. Gatti and Montanari have become targets for violent threats on Facebook. Accusers denounce their meticulous laboratory work as “pseudoscience” and call for the two scientists to be “beaten until they bleed,” “punched,” “kicked” and “taken out of commission” so as to make them “understand that they need to remain silent.”

An army of pharmaceutical industry trolls and bloggers have pressured the badly shaken journal editor to “unpublish” the study, which was published after a rigorous peer review process. Although these tactics have succeeded in rattling the editor, the article stands. Gatti and Montanari believe so strongly in the integrity of their findings that they have made known that they will sue if the journal takes down the paper.

Despite the passion of their attacks, industry bloggers have been hard pressed to find substantive fault with Gatti/Montanari’s methodologies. An industry flack, Guido Silvestri, working at a vaccine center in Atlanta, took a bungling shot at the Gatti-Montanari study on Italian Facebook by misapplying a nineteenth-century law of chemistry called Avogadro’s number. Silvestri misinterpreted Avogadro’s law, which applies only to gases and cannot calculate nanoparticle concentrations. According to Drs. Gatti and Montanari, the medical doctor “erred by 13 orders of magnitude but did not even understand his own mistake.”

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Gatti and Montanari believe that the immune system is permanently damaged by these composite particles, which constitute “a bigger-sized compound that is not biodegradable and can induce adverse effects,” including both immediate and deferred autoimmune problems.

Why the Vaccine Contaminant Study is Important

Gatti and Montanari work in the emerging fields of nanopathology and nanotoxicology. The two researchers coined the term “nanopathology” in the early 2000s after finding that nanoparticles (particles less than 100 nanometers in size) “induce far more severe [health] effects” than larger particles. As they explain, the minute size makes it “extremely easy” for the particles to infiltrate the body’s tissues.

Drs. Gatti and Montanari used cutting-edge electron microscope technology to physically examine inorganic, particulate contaminants in vaccines and identify their chemical composition. They assessed 44 vaccines manufactured in Italy and France (43 human vaccines and one veterinary vaccine), taking pains to include different types, batches and years of production. In every human vaccine, Gatti and Montanari found wide-ranging contamination, including minute particles of lead or stainless steel in all of the vaccine samples analyzed; chromium in over half (25/44); tungsten in almost a fifth (8/44); and many other varieties of metallic particles.

Ironically, the single veterinary vaccine tested as “clean,” proving that it is possible to manufacture a debris-free vaccine. Gatti and Montanari believe that the pristine hog vaccine is a homage to ham, a sacred culinary and agricultural product in Italy. Hog farmers, aware that aluminum adjuvants in vaccines harm their meat, had enough clout to successfully lobby for uncontaminated veterinary vaccines.

One of the study’s most sobering findings was the detection of “organic-inorganic composites” that represent a “nano-bio-interaction” between the inorganic particulate matter and the organic (protein) vaccine components. Gatti and Montanari believe that the immune system is permanently damaged by these composite particles, which constitute “a bigger-sized compound that is not biodegradable and can induce adverse effects,” including both immediate and deferred autoimmune problems.

The Questions We Should Be Asking

Dr. Gatti has considered several hypotheses about the origins of the vaccine contamination, including shoddy line protocols in the manufacturing process. According to Gatti, “The facilities need to be really clean to ensure that dust and pollutants do not find their way into the vaccines. If the labs do not have proper filtration, then this kind of contamination is very possible. And unfortunately, there are no regulations requiring manufacturers to do this kind of quality control, even though the manufacturers know that there is something wrong.” In short, the manufacturers “see no need to spend more money on quality control.”

Gatti and Montanari see an urgent need for more studies of the association between the debris and vaccine-related adverse events. “We still don’t know whether the kinds of adverse events that result from vaccines are the result of the aluminum adjuvants or the nano-bio interactions or something else. That is why it is so important to study the effects of the nano-bio materials inside the blood and body.”

Exposure via injection is known to induce toxicity reactions as compared to inhalation or ingestion. A study in mice found that exposure route was a crucial factor influencing toxicity and that orally administered compounds exhibited a “decrease of toxicity…as compared with injection route.” Scientists agree that “engineered metal-based nanoparticles can translocate to tissues,” and, in Gatti’s and Montanari’s view, when they enter the body via injection, “they stay there forever.”

Another point is that the barrage of toxic adjuvants and ingredients in vaccines (including aluminum and thimerosalformaldehydeantibiotics and “adjuvant systems” involving squalene and polysorbate 80) “have a synergistic action, thus…enhancing their aggressive potential.” Toxicologists know that, with toxins, one plus one rarely equals two but, in Dr. Gatti’s words, “always a higher number.”

Finally, Dr. Gatti observes that “the contaminants might not be homogenously distributed within a given batch of vaccines. For example, the bottom of the batch might be more contaminated than the top, which could explain why some people don’t have reactions and other people do.”

Drs. Gatti and Montanari outline a number of research topics that should form the basis of serious efforts to improve vaccine safety:

  • Meaningfully study the adverse health effects of aluminum adjuvants
  • Analyze the brains of infants who die immediately following vaccination
  • Continue to monitor micro- and nanoparticle contamination in new and existing vaccines
  • Conduct animal model studies to assess the effects of micro- and nanoparticle contamination
  • Assess the injection process itself, given the use of metallic syringes polished with tungsten carbide that may leave some metallic residue
…the barrage of toxic adjuvants and ingredients in vaccines (including aluminum and thimerosal, formaldehyde, antibiotics and “adjuvant systems” involving squalene and polysorbate 80) “have a synergistic action, thus. . .enhancing their aggressive potential.”

Follow the Money

Unfortunately, in Italy, as in the United States, serious studies of vaccine safety face practically insurmountable headwinds. Italy’s Minister of Health, Beatrice Lorenzin, has explicitly “forbidden” any research on nanoparticles in vaccines. Lorenzin aggressively pushed passage of the law mandating children’s vaccines. Lorenzin, a former journalist, has no formal education beyond ordinary high school. Gatti and Montanari point out that she has “no knowledge of chemistry or biology.” They add, “If you mention the nanoparticle research to her, she gets mad.” According to the two researchers, Lorenzin “does not understand science, but she understands money” and relies for guidance on Dr. Ranieri Guerra, the Ministry of Health’s Director General for Prevention. Guerra served on the board of Italy’s Smith Kline Foundation. The Smith Kline Foundation receives financial support from founding partner GlaxoSmithKline (GSK). Consumer advocacy organizations and legislators in Italy have harshly criticized Guerra for conflicts of interest.

Italians protest mandatory vaccinations in July, 2017
Italians protest mandatory vaccinations – July, 2017

A year before the passage of the new vaccine mandate, an April 2016 news report indicated that GSK-Italy was “doubling down” on its vaccine portfolio and “betting 1 billion euros on Italy.” The drug company is beefing up a vaccine research and development hub in Siena and a vaccine manufacturing plant in Rosia. The article quoted the global president of GSK Vaccines, who characterized GSK’s vaccine branch as a “motor of innovation” and guarantor of the company’s long-term sustainability. The same GSK executive described Italy’s pivotal role as a vaccine research and production hub as “a not insignificant step” toward further “progress” in the vaccine marketplace.

Italian officials have historically been important supporters of aggressive vaccine policies. In 2009–2010, the Italian government (via the taxpayers) purchased 24 million bird flu vaccines that were never used. The unused vaccines were thrown away but, says Dr. Montanari, “the companies made a lot of money.” Referring to this situation as a “flop,” the Italian newspaper La Repubblica reported that the country was left holding the bag for the cost of the unused vaccines while the apparent “pandemic” evaporated into thin air.

Dr. Montanari views the new vaccine law as both a social and medical experiment: “The government and the pharmaceutical industry want to see what happens when 60 million people are forced to be vaccinated.”

Meme of Nuremberg Code

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The Powerful Aspirin Alternative Your Doctor Never Told You About

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In Brief

  • The Facts:

    This article was written by Sayer Ji, Founder of Greenmedinfo,com where it was originally posted. Published here with permission.

  • Reflect On:

    Given the newly released cardiovascular disease prevention guidelines recommending against daily low-dose aspirin use, natural, safe and effective alternatives are needed now more than ever.

In a previous article titled “The Evidence Against Aspirin and For Natural Alternatives,” we discussed the clear and present danger linked with the use of aspirin as well as several clinically proven alternatives that feature significant side benefits as opposed to aspirin’s many known side effects.

Since writing this article, even more evidence has accumulated indicating that aspirin’s risks outweigh its benefits. Most notably, a 15-year Dutch study published in the journal Heart found that among 27,939 healthy female health professionals (average age 54) randomized to receive either 100 mg of aspirin every day or a placebo the risk of gastrointestinal bleeding outweighed the benefit of the intervention for colorectal cancer and cardiovascular disease prevention in those under 65 years of age. Most recently, last month, new cardiovascular disease prevention guidelines submitted jointly by the American College of Cardiology and the American Heart Associated and published in the Journal of the American College of Cardiology, earlier this year, contradict decades of routine medical advice by explicitly advising against the daily use of low-dose or baby aspirin (75-100 mg) as a preventive health strategy against stroke or heart attack, in most cases.

Of course, aspirin is not alone as far as dangerous side effects are concerned. The entire non-steroidal anti-inflammatory (NSAID) category of prescription and over-the-counter drugs is fraught with serious danger. Ibuprofen, for instance, is known to kill thousands each year, and is believed no less dangerous than Merck’s COX-2 inhibitor NSAID drug Vioxx which caused between 88,000-140,000 cases of serious heart disease in the five years it was on the market (1999-2004). Tylenol is so profoundly toxic to the liver that contributing writer Dr. Michael Murray recently asked in his Op-Ed piece, “Is it Time for the FDA to Remove Tylenol From the Market?” Just as serious are tylenol’s empathy destroying properties that were only identified four years ago.

Given the dire state of affairs associated with pharmaceutical intervention for chronic pain issues, what can folks do who don’t want to kill themselves along with their pain?

Pine Bark Extract (Pycnogenol) Puts Aspirin To Shame

When it comes to aspirin alternatives, one promising contender is pycnogenol, a powerful antioxidant extracted from French maritime pine bark, backed by over 40 years of research, the most compelling of which we have aggregated on GreenMedInfo.com here: Pycnogenol Research. Amazingly, you will find research indexed there showing it may have value for over 80 health conditions.

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In 1999, a remarkable study published in the journal Thrombotic Research found that pycnogenol was superior (i.e. effective at a lower dosage) to aspirin at inhibiting smoking-induced clotting, without the significant (and potentially life-threatening) increase in bleeding time associated with aspirin use. The abstract is well worth reading in its entirety:

“The effects of a bioflavonoid mixture, Pycnogenol, were assessed on platelet function in humans. Cigarette smoking increased heart rate and blood pressure. These increases were not influenced by oral consumption of Pycnogenol or Aspirin just before smoking. However, increased platelet reactivity yielding aggregation 2 hours after smoking was prevented by 500 mg Aspirin or 100 mg Pycnogenol in 22 German heavy smokers. In a group of 16 American smokers, blood pressure increased after smoking. It was unchanged after intake of 500 mg Aspirin or 125 mg Pycnogenol. In another group of 19 American smokers, increased platelet aggregation was more significantly reduced by 200 than either 150 mg or 100 mg Pycnogenol supplementation. This study showed that a single, high dose, 200 mg Pycnogenol, remained effective for over 6 days against smoking-induced platelet aggregation. Smoking increased platelet aggregation that was prevented after administration of 500 mg Aspirin and 125 mg Pycnogenol. Thus, smoking-induced enhanced platelet aggregation was inhibited by 500 mg Aspirin as well as by a lower range of 100-125 mg Pycnogenol. Aspirin significantly (p<0.001) increased bleeding time from 167 to 236 seconds while Pycnogenol did not. These observations suggest an advantageous risk-benefit ratio for Pycnogenol.” [emphasis added]

As emphasized in bold above, pycnogenol unlike aspirin did not significantly increase bleeding time. This has profound implications, as aspirin’s potent anti-platelet/’blood thinning’ properties can also cause life-threatening hemorrhagic events. If this study is accurate and pycnogenol is more effective at decreasing pathologic platelet aggregation at a lower dose without causing the increased bleeding linked to aspirin, then it is clearly a superior natural alternative worthy of far more attention by the conventional medical establishment and research community than it presently receives.

Not Just A Drug Alternative

Pycnogenol, like so many other natural interventions, has a wide range of side benefits that may confer significant advantage when it comes to reducing cardiovascular disease risk. For instance, pycnogenol is also:

  • Blood Pressure Reducing/Endothelial Function Enhancer: A number of clinical studies indicate that pycnogenol is therapeutic for those suffering with hypertension. Pycnogenol actually addresses a root cause of hypertension and cardiovascular disease in general, namely, endothelial dysfunction (the inability of the inner lining of the blood vessels to function correctly, e.g. fully dilate).[1] It has been shown to prevent damage in microcirculation in hypertensive patients, as well as reducing the dose of blood pressure drugs in hypertensive patients,[2]including hypertensive diabetic patients.[3] It has even been found to reduce intraocular hypertension found in glaucoma patients.[4]
  • Anti-Inflammatory Effects: There is a growing appreciation among the medical community that inflammation contributes to cardiovascular disease. Several markers, including C-reactive protein are now being fore grounded as being at least as important in determining cardiovascular disease risk as various blood lipids and/or their ratios, such as low-density lipoprotein (LDL). Pycnogenol has been found to reduce C-reactive protein in hypertensive patients.[5] Pycnogenol has been found to rapidly modulate downward (inhibit) both Cox-1 and Cox-2 enzyme activity in human subjects, resulting in reduced expression of these inflammation-promoting enzymes within 30 minutes post-ingestion.[6] Another observed anti-inflammatory effect of pycnogenol is its ability to down-regulate the class of inflammatory enzymes known as matrix metalloproteinases (MMPs).[7] Pycnogenol has also been found to significantly inhibit NF-kappaB activation, a key body-wide regulator of inflammation levels whose overexpression and/or dysregulation may result in pathologic cardiovascular manifestations.[8] Finally, pycnogenol has been found to reduce fibrinogen levels, a glycoprotein that contributes to the formation of blood clots; fibrinogen has been identified as an independent risk factor for cardiovascular disease.[9]
  • The Ideal Air Travel Companion: In a previous article entitled, “How Pine Bark Extract Could Save Air Travelers Lives,” we delve into a compelling body of research that indicates pycnogenol may be the perfect preventive remedy for preventing flight-associated thrombosis, edema, and concerns related to radiotoxicity and immune suppression.

Given the evidence for pycnogenol’s pleotrophic cardioprotective properties, we hope that pycnogenol will become more commonly recommended by health care practitioners as the medical paradigm continues to evolve past its reliance on synthetic chemicals, eventually (we hope) returning to natural, increasingly evidence-based interventions. However, it is important that we don’t fall prey to the one-disease-one-pill model, convincing ourselves to focus on popping pills – this time natural ones – as simply countermeasures or ‘insurance’ against the well-known harms associated with the standard American diet, lack of exercise and uncontrolled stress. The ultimate goal is to remove the need for pills altogether, focusing on preventing cardiovascular disease from the ground up and inside out, e.g. letting high quality food, clean water and air, and a healthy attitude nourish and sustain your health and well-being.


References

[1] Ximing Liu, Junping Wei, Fengsen Tan, Shengming Zhou, Gudrun Würthwein, Peter Rohdewald. Pycnogenol, French maritime pine bark extract, improves endothelial function of hypertensive patients. Life Sci. 2004 Jan 2;74(7):855-62. PMID: 14659974

[2] Gianni Belcaro, Maria Rosaria Cesarone, Andrea Ricci, Umberto Cornelli, Peter Rodhewald, Andrea Ledda, Andrea Di Renzo, Stefano Stuard, Marisa Cacchio, Giulia Vinciguerra, Giuseppe Gizzi, Luciano Pellegrini, Mark Dugall, Filiberto Fano. Control of edema in hypertensive subjects treated with calcium antagonist (nifedipine) or angiotensin-converting enzyme inhibitors with Pycnogenol. Clin Appl Thromb Hemost. 2006 Oct;12(4):440-4. PMID: 17000888

[3] Sherma Zibadi, Peter J Rohdewald, Danna Park, Ronald Ross Watson. Reduction of cardiovascular risk factors in subjects with type 2 diabetes by Pycnogenol supplementation. Nutr Res. 2008 May;28(5):315-20. PMID: 19083426

[4] Robert D Steigerwalt, Belcaro Gianni, Morazzoni Paolo, Ezio Bombardelli, Carolina Burki, Frank Schönlau. Effects of Mirtogenol on ocular blood flow and intraocular hypertension in asymptomatic subjects. Mol Vis. 2008;14:1288-92. Epub 2008 Jul 10. PMID: 18618008

[5] Maria Rosaria Cesarone, Gianni Belcaro, Stefano Stuard, Frank Schönlau, Andrea Di Renzo, Maria Giovanna Grossi, Mark Dugall, Umberto Cornelli, Marisa Cacchio, Giuseppe Gizzi, Luciano Pellegrini. Kidney flow and function in hypertension: protective effects of pycnogenol in hypertensive participants–a controlled study. J Cardiovasc Pharmacol Ther. 2010 Mar;15(1):41-6. Epub 2010 Jan 22. PMID: 20097689

[6] Angelika Schäfer, Zuzana Chovanová, Jana Muchová, Katarína Sumegová, Anna Liptáková, Zdenka Duracková, Petra Högger. Inhibition of COX-1 and COX-2 activity by plasma of human volunteers after ingestion of French maritime pine bark extract (Pycnogenol). Biomed Pharmacother. 2006 Jan;60(1):5-9. Epub 2005 Oct 26. PMID: 16330178

[7] Tanja Grimm, Angelika Schäfer, Petra Högger. Antioxidant activity and inhibition of matrix metalloproteinases by metabolites of maritime pine bark extract (pycnogenol). Wei Sheng Yan Jiu. 2011 Jan;40(1):103-6. PMID: 14990359

[8] Tanja Grimm, Zuzana Chovanová, Jana Muchová, Katarína Sumegová, Anna Liptáková, Zdenka Duracková, Petra Högger. Inhibition of NF-kappaB activation and MMP-9 secretion by plasma of human volunteers after ingestion of maritime pine bark extract (Pycnogenol). J Inflamm (Lond). 2006;3:1. Epub 2006 Jan 27. PMID: 16441890

[9] G Belcaro, M R Cesarone, S Errichi, C Zulli, B M Errichi, G Vinciguerra, A Ledda, A Di Renzo, S Stuard, M Dugall, L Pellegrini, G Gizzi, E Ippolito, A Ricci, M Cacchio, G Cipollone, I Ruffini, F Fano, M Hosoi, P Rohdewald. Variations in C-reactive protein, plasma free radicals and fibrinogen values in patients with osteoarthritis treated with Pycnogenol. Redox Rep. 2008;13(6):271-6. PMID: 19017467

Originally published: 2017-07-23

Article updated: 2019-04-11


Link to original article


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Long-Term Consequences of Mumps Vaccination: Many Unanswered Questions

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This is Part II of a two-part series on mumps. Part I discussed how mumps vaccination and the flawed mumps component of Merck’s MMR vaccine are fostering dangerous mumps outbreaks in adolescents and young adults.

It has been about five decades since the U.S. Food and Drug Administration (FDA) approved Merck’s first mumps vaccine. The company began launching combination MMR (measles, mumps and rubella) vaccines in the 1970s. Coincidentally—or not—an infertility crisis has been brewing over roughly the same time period, with dramatic declines in sperm counts and record-lowfertility levels. However, few investigators seem interested in assessing whether mumps outbreaks in highly vaccinated populations of teens and young adults could be having long-termeffects on fertility or other health indicators.

As described in Part I, childhood MMR vaccination has been an unmitigated disaster where mumps is concerned, deferring mumps infection to older ages and leaving adolescents and young adults vulnerable to serious reproductive complications. Public health reports show that the vast majority of mumps cases and outbreaks occur in youth who have been fully vaccinatedwith the prescribed two-dose MMR series, supporting a hypothesis of “waning immunity after the second dose.” FDA and Centers for Disease Control and Prevention (CDC) officials even admitthat mumps outbreaks in the post-vaccination era “typically involve young adults,” and that vaccination is failing to protect those who are college-age and above.

Myopically, many vaccine experts have called for a third MMR dose—or even “booster dosing throughout adulthood”—even though the FDA’s and CDC’s own research shows that MMR boosters in college-age youth barely last one year. As alleged in whistleblower lawsuits wending their way through the courts over the past eight years, Merck presented the FDA with a “falsely inflated efficacy rate” for the MMR’s mumps component, using animal antibodies and other fraudulent tactics to fool FDA—and the public—into believing that the vaccine was effective.

When infection arises after puberty, however, mumps is no laughing matter, presenting an increased risk of complications such as hearing loss, encephalitis and inflammation of the reproductive organs.

Mumps after puberty is no laughing matter

Around the time that the first mumps vaccine came on the market, the 1967 children’s classic The Great Brain humorously depicted mumps infection in childhood as a mere nuisance. The book’s young protagonist goes out of his way to intentionally infect himself with mumps so that he can beat his two brothers to the recovery finish line—and he experiences no adverse consequences other than his siblings’ annoyance.

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When infection arises after puberty, however, mumps is no laughing matter, presenting an increased risk of complications such as hearing loss, encephalitis and inflammation of the reproductive organs. About one in three postpubertal men with mumps develops orchitis(inflammation of the testes), which can damage sperm, affect testosterone production and contribute to subfertility and infertility. During a mumps outbreak in England in the mid-2000s, mumps orchitis accounted for 42% of all hospitalized mumps cases; the researchers attributed this outcome—which was the most common reason for hospitalization—to “the high attack rates in adolescents and young adults” that occurred “despite high coverage with two-dose MMR.” An analysis of a 2006 mumps outbreak in the U.S. reported that male patients were over three times more likely than female patients to experience complications, “due primarily to orchitis.”

An estimated 5% to 10% of postpubertal women will develop oophoritis (swelling of the ovaries) following mumps infection. Oophoritis is associated with premature menopause and infertility, but mumps-related oophoritis has garnered little notice.

Mumps infections are often asymptomatic or produce nonspecific symptoms such as fever, while cases of orchitis may present with no other mumps symptoms. Nonetheless, public health officials advise clinicians that orchitis is an instant cue to test for mumps virus, and testing often reveals elevated mumps antibodies. In a case report of MMR failure, British clinicians isolated a novel genetic strain of mumps virus from the patient’s semen two weeks after the onset of orchitis and found mumps RNA in the semen 40 days later; they also noted “the appearance of anti-sperm antibodies,” with “potential long-term adverse effects on the patient’s fertility.”

In 2017, researchers who reviewed 185 studies conducted in Western nations found that sperm counts had plummeted by 50% to 60% between 1973 and 2011—an average decrease of 1.4% annually. Commenting on this work, one analyst estimated that 20% to 30% of young men in Europe and North America have sperm concentrations associated with a reduced ability to father a child. Given estimates that as much as 40% of reproductive problems have to do with the male partner, there is agreement on the importance of “finding and eliminating [the] hidden culprits in the environment” that most researchers believe are to blame.

An estimated 5% to 10% of postpubertal women will develop oophoritis (swelling of the ovaries) following mumps infection. Oophoritis is associated with premature menopause and infertility, but mumps-related oophoritis has garnered little notice.

MMR’s and MMRV’s potential to impair fertility never studied

Merck has not evaluated either of its two MMR vaccines—the MMR-II and the MMR-plus-varicella (MMRV) vaccine—for their potential to impair fertility. Whether such testing would unearth direct effects on fertility (as appears to be possible with HPV vaccination in women) is thus unknown. However, mumps vaccination undeniably increases reproductive-age individuals’ risk of mumps infection and, in the process, increases the risk of fertility-altering complications. These facts alone should be attracting far more attention.

Unfortunately, because clinicians already tend to underdiagnose mumps infection and underestimate mumps complications, it is likely that they are failing to recognize possible vaccine-induced reproductive health consequences of mumps infection in their adolescent and young adult patients. In one university outbreak, “most physicians…did not suspect mumps,” and even when they became aware of the outbreak, “diagnosing mumps was not always straightforward.” Moreover, although differentiating between vaccine strains of mumps virus and wild types could provide valuable information, few clinicians have the capacity or inclination to perform testing of this type. A Japanese study of cerebrospinal fluid and saliva from patients with mumps complications found vaccine strain in nearly all of the samples and noted the information’s importance in helping determine whether the complications were vaccine-related.

Those who have sought to understand mumps vaccines’ poor performance point to a mixture of explanatory factors. These include waning immunity, the high population density and close quarters encountered in settings such as college campuses, incomplete vaccine-induced immunity to wild virus as well as viral evolution such that “the vaccine triggers a less potent reaction against today’s mumps viruses than those of 50 years ago.” However, some also quietly admit that individuals with “mild vaccine-modified disease” could be perpetuating the chain of transmission. This latter point ought to be raising questions about the logic and wisdom of administering further rounds of MMR boosters during outbreaks while ignoring the problems created by the doses already given.

… some individuals respond poorly to mumps vaccination and vaccine-induced antibody levels correlate poorly with protection from mumps infection, irrespective of the number of additional doses of mumps-containing vaccine they receive.

Most scientists appear to be either resigned to ongoing mumps outbreaks in vaccinated populations or actually accept periodic outbreaks as the cost of doing business. Publications by FDA and CDC researchers reveal these agencies’ awareness that some individuals respond poorly to mumps vaccination and that vaccine-induced antibody levels correlate poorly with protection from mumps infection, “irrespective of the number of additional doses of mumps-containing vaccine they receive.” Considering the effects on fertility, the generally abysmal track record of mumps vaccination and Merck’s fraudulent claims about efficacy, it is hard to fathom medical and public health experts’ complacency about current mumps vaccines and vaccine policies.


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Investigation Shows The MMR Vaccine Was Approved Based On Small Studies Showing Disturbing Results

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In Brief

  • The Facts:

    A FOIA request by Del Bigtree reveals that the 8 studies supporting the release of the MMR vaccine were only 6 weeks long, used only 800 children, and led to damaging respiratory and gastrointestinal illnesses to many of the children.

  • Reflect On:

    Are we ready to collectively deal with the implications of ongoing revelations of industry malfeasance with regards to vaccines that for some may require a shift in long-held beliefs?

Amidst a rash of efforts to bring forward mandatory vaccination in pockets of the United States is the recent move in New York City to declare a public health emergency Tuesday over a measles outbreak and order mandatory vaccinations in one neighborhood for people who may have been exposed to the virus.

Mayor Bill de Blasio announced the unusual order to address what he said was a measles “crisis” in Brooklyn’s Williamsburg section, where more than 250 people have gotten measles since September. The order applies to anyone living, working or going to school in four zip codes in the neighborhood. The declaration requires all unvaccinated people who may have been exposed to the virus to get the vaccine, including children over 6 months old. People who ignore the order could be fined $1,000.

Challenging Assumptions

This kind of invasive move gives rise to several serious questions, including challenging many of the assumptions that are necessarily made to justify such a move.

Assumption #1: People who may have been infected with the measles should get vaccinated immediately. De Blasio wants people who may have been infected with the measles to get vaccinated. The assumption here is that the vaccine would actually help someone who has the virus by preventing them from getting the measles or preventing them from spreading it to others. But this just doesn’t stand to reason. If someone is already infected, getting a measles vaccine will not prevent the outbreak. That’s not what a vaccine is designed for. And while the person is going through the 2-week period it takes for the vaccine to take hold, it’s quite possible that this will weaken the immune response to the actual measles infection the person has. Quarantining people suspected of being infected would be the sensible response, not vaccinating. If they happen to have the measles, no problem. Once they recover they will then be immune for life.

Assumption #2: The MMR Vaccine Can Create Herd Immunity. There is an article in the Huffington post entitled ‘I’m No Anti-Vaxxer, But the Measles Vaccine Can’t Prevent Outbreaks,’ in which Dr. Gregory Poland, who strongly advocates for vaccines, notes that outbreaks are often initiated and spread by people who have been fully vaccinated against the measles–over 50% in the case of a 2011 outbreak in Quebec. How is this possible? While this Quebec outbreak happened within a community that supposedly had achieved herd-immunity status of over 95% vaccinated, the facts are, as the article notes, that “9 per cent of children having two doses of the vaccine, as public health authorities now recommend, will have lost their immunity after just seven and a half years. As more time passes, more lose their immunity.” Therefore, herd immunity for measles is simply impossible to achieve with this vaccine.

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Assumption #3: The MMR Vaccine, in de Blasio’s words, is ‘safe, effective, and life-saving.’ The claim that the MMR vaccine is ‘life-saving’ does not stand up to simple statistics, as we detail in our article ‘Statistics Show The MMR Vaccine Kills More People Than The Measles Does.’ Whether it is effective, we have already seen that it is incapable of creating herd immunity, wanes over time, does not work at all for some people, and in some of the latest outbreaks the majority of people infected were fully vaccinated. Is it safe? This is the important question we cover in the next section.

The Studies That Stand Behind The Approval Of the MMR Vaccine

The pharmaceutical industry, as well as governmental regulatory bodies like the CDC and the FDA, assure the public that they take the safety of vaccines seriously, and that there is irrefutable science behind the notion that vaccines are safe in terms of the studies that their approval is based on.

However, a Freedom of Information Act request by Del Bigtree has revealed absolutely startling information about the studies that supported the approval of the MMR vaccines that have been injected into our children. To begin with, only 8 studies were conducted and the total combined number of children participating in the studies was only a little over 800! Furthermore, the studies only recorded symptoms for the first 6 weeks after the vaccines were given, unlike many other drug studies that follow symptoms for 5 years or more. And finally, the study revealed serious side-effects in those receiving the vaccine, including a highly significant number of participants who suffered upper respiratory illness and gastrointestinal illness, which has been linked to autism.

In our latest episode of The Collective Evolution Show on CETV, Joe, Arjun and I discussed New York’s mandatory vaccination order as well as Del Bigtree’s analysis of the MMR studies he received and the reason that Big Pharma not only does not want to do proper, large-scale studies on the safety of vaccines, but they also want to try to prevent other researchers like Dr. Christopher Exley from doing so as well.

You can watch the full episode of The Collective Evolution Show where we talk about this subject in more detail here.

You can go here to see the full episode of ‘The Highwire’ where Del Bigtree breaks down the MMR studies in question.

The Takeaway

The veils of illusion that have been masking the truth are lifting as our consciousness awakens. Transparency is coming, though how long it takes will depend on our continued efforts to dig for and spread the truth far and wide.

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