Connect with us

Awareness

The Top 6 Reasons Why Parents Are Choosing Not To Vaccinate Their Kids

Published

on

More and more parents around the globe are choosing to opt out of vaccinating themselves and their children, and the “pro-vaccine” community is not happy, criticizing parents for their decision to not vaccinate. At the end of the day it’s not really about “pro-vaccination” or “anti-vaccination,” however; it’s not about pointing fingers or pitting one against the other, it’s simply about looking at all of the information from a neutral standpoint. It’s about asking questions and communicating so people can make the best possible decisions for themselves and their children. Parents love their kids and the vaccine “controversy” has made it difficult for many parents to know what to do.

advertisement - learn more

It’s not just parents, it’s doctors too.

A new study published in the journal EbioMedicine outlines this point, stating in the introduction:

Over the past two decades several vaccine controversies have emerged in various countries, including France, inducing worries about severe adverse effects and eroding confidence in health authorities, experts, and science (Larson et al., 2011). These two dimensions are at the core of the vaccine hesitancy (VH) observed in the general population. VH is defined as delay in acceptance of vaccination, or refusal, or even acceptance with doubts about its safety and benefits, with all these behaviors and attitudes varying according to context, vaccine, and personal profile, despite the availability of vaccine services (Group, 2014,Larson et al., 2014, Dubé et al., 2013). VH presents a challenge to physicians who must address their patients’ concerns about vaccines and ensure satisfactory vaccination coverage.

The study concludes with the observation that “after repeated vaccine controversies in France, some vaccine hesitancy exists among French GPs, whose recommendation behaviours depend on their trust in authorities, their perception of the utility and risks of vaccines, and their comfort in explaining them.”

As a result, the study explains, “16% to 43% of GPs sometimes or never recommended at least one specific vaccine to their target patients.”

advertisement - learn more

The percentages differ because the study asks about specific vaccines, and whether they are recommended never, sometimes, often, or always. You can refer to the study for more details.

The authors’ overall findings “suggest that VH [vaccine hesitancy] is prevalent among French GPs. It may make them ill at ease in addressing their patients’ concerns about vaccination, which in turn might reinforce patients’ VH.”

Again, this isn’t a secret. Another study (out of many, cited in the France publication) outlines how “more research is needed to understand why some health professionals, trained in medical sciences, still have doubts regarding the safety and effectiveness of vaccination.”

Parents who are choosing not to vaccinate their children are not just doing it based on belief, they are doing it based on science, some of which will be presented in this article, and all of which does not get the mainstream representation that “pro-vaccine” science does. Parents who choose not to vaccinate themselves or their children are clearly intelligent, and should not be ridiculed for their concern. On the other hand, parents who are choosing to vaccinate their children are also intelligent. Those who choose to vaccinate should not be made out to be the ones who have made the “right” decision when there is evidence on both sides of the coin that clearly shows parents who are not vaccinating their children could also be making the “right” decision.

I’d also like to state that there are multiple vaccines. Some may be safe, some may not be. There are also criticisms of all the studies mentioned, as well as bias. That being said, all of the studies in this article, with the exception of one or two, have been published in credible peer-reviewed scientific journals. That should not take away from the important work of many independent scientists from all over the world.

This article will present a few of the many reasons why parents are choosing to not vaccine their children.

 # 1  The Vaccine/Autism Controversy

The idea that vaccines might be linked to autism can be triggering for a lot of people. Some people won’t even entertain the idea, or look at information that suggests there could be a link, but the truth is, there are plenty of studies showing one. At the same time, there are plenty of studies that stress there is no link, and that vaccines are not in any way linked to autism. I am referring to both peer-reviewed publications and important independent research that’s not sponsored by the vaccine manufacturers themselves.

STUDIES SHOWING VACCINES ARE NOT LINKED TO AUTISM

Starting off with some of the most recent data available, a study published in the journal Vaccine determined that:

  • There was no relationship between vaccination and autism
  • There was no relationship between vaccination and ASD (autism spectrum disorder)
  • There was no relationship between  the MMR vaccination and autism/ASD
  • There was no relationship between autism/ASD and thimerosal
  • There was no relationship between austism/ASD and mercury (Hg)

The study concluded that vaccinations are not associated with the development of autism or autism spectrum disorder. It was a meta-analysis done by researchers at the University of Sydney, in Australia. It examined ten studies involving more than one million children affirming that vaccines don’t cause autism.

In March 2013, the Journal of Paediatrics published a study titled “Increasing exposure to Antibody-Stimulating Proteins and Polysaccharides (antigens) in Vaccines is Not Associated with Risk of Autism.” The study found that vaccines given during the first couple of years of life are not related to the risk of developing an ASD diagnosis. They analyzed data from a case-control study conducted in three managed care organizations (MCOs) of 256 children with autism spectrum disorder (ASD) and 752 control children matched on birth year, sex and MCO.

Another study published in the Journal of Paediatrics titled “Thimerosal exposure in infants and developmental disorders: a retrospective cohort study in the United Kingdom does not support a causal association” concluded that, with the possible exception of tics, there was no evidence that thimerosal exposure via the DTP/DT vaccines causes any neurodevelopment disorders.

A report published in the Canadian Journal of Neurological Sciences emphasized how there is an “overwhelming” majority showing no causal association between the Measles-Mumps-Rubella (MMR) and autism. It also determined that there was no convincing evidence that thimerosal has any role in autism.

A study published straight from the CDC and National Immunization program determined that “the evidence is now convincing that the measles-mumps-rubella vaccines do not cause autism or any type of autism spectrum disorder.”

The list literally goes on and on here. Study after study in peer-reviewed scientific journals claim no link between vaccines/vaccine ingredients and autism.

This is why many people reject the notion that vaccines could be linked to autism. But that rejection is usually the result of simply not being exposed to the science on the opposing side.

STUDIES SHOWING VACCINES COULD BE LINKED TO AUTISM

As I did in the previous section, I will begin with a couple of more recent studies. If vaccines aren’t linked to autism, why are scientists/researchers emphasizing that they could be, and showing that there is a possible link? These studies are contradictory to the ones above, yet conducted by people with the same qualifications and published in peer-reviewed scientific journals. Let’s take a look.

A study published in the Journal of Toxicology by scientists from the University of British Colombia, the University of Louisiana, and MIT outlines how up until the 1820s — when the industrial extraction of aluminum made it possible to bring it into our food, manufacturing, medicines, and more — aluminum was almost completely absent from the biosphere. The paper outlines how aluminum is harmful to the central nervous system (CNS), “acting in a number of deleterious ways and across multiple levels to induce biosemiotic entropy.”

Biosemiotic entropy refers to the corruption of biological messages from genetics, epigenetics, proteins, cells, tissues and organs. The paper points out how CNS problems are correlated with diseases like autism spectrum disorder, and makes a strong argument that aluminum adjuvants in the form of pediatric vaccines could be contributing to increased rates of autism spectrum disorders (page 8).

One of the authors of this paper, Dr. Chris Shaw, a neurologist at the University of British Columbia, explains the danger of putting aluminum in vaccines. When aluminum comes from a vaccine, it stays in the body, and studies have shown that the adjuvants do not stay localized but rather travel to the brain, where they can be detected up to a year after the injection.

A study published in the journal Current Medical Chemistry  in 2011 stated:

Aluminum is an experimentally demonstrated neurotoxin and the most commonly used vaccine adjuvant. Despite almost 90 years of widespread use of aluminum adjuvants, medical science’s understanding about their mechanisms of action is still remarkably poor. There is also a concerning scarcity of data on toxicology and pharmacokinetics of these compounds. In spite of this, the notion that aluminum in vaccines is safe appears to be widely accepted. Experimental research, however, clearly shows that aluminum adjuvants have a potential to induce serious immunological disorders in humans. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications and may thus have profound and widespread adverse health consequences.

The paper points out how aluminum could be a culprit in the development of a wide body of neurodegenerative disease, one of them being autism.

Here is a statement I took from the paper. For the specific citations you can look at the actual paper:

The issue of vaccine safety thus becomes even more pertinent given that, to the best of our knowledge, no adequate clinical studies have been conducted to establish the safety of concomitant administration of two experimentally-established neurotoxins, aluminum and mercury, the latter in the form of ethyl mercury (thimerosal) in infants and children. Since these molecules negatively affect many of the same biochemical processes and enzymes implicated in the etiology of autism, the potential for a synergistic toxic action is plausible [31, 47]. Additionally, for the purpose of evaluating safety and efficacy, vaccine clinical trials often use an aluminium-containing placebo, either containing the same or greater amount of aluminum as the test vaccine [48-51]. Without exception, these trials report a comparable rate of adverse reactions between the placebo and the vaccine group (for example, 63.7% vs 65.3% of systemic events and 1.7% vs 1.8% of serious adverse events respectively [51]).

The paper also points to the fact that brain inflammatory responses have long been recognized as a factor in etiology of many neurodegenerative diseases like autism, and provides a host of citations for that as well.

Shaw and Tomljenovic also published a paper in 2011 that was approved for publication in the Journal of Inorganic Biochemistry that stated:

We show that Al-adjuvanted vaccines may be a significant etiological factor in the rising prevalence of ASD. According to the FDA, vaccines represent a special category of drugs as they are generally given to healthy individuals. Further according to the FDA, “this places significant emphasis on their vaccine safety.” While the FDA does set an upper limit for Aluminum in vaccines at no more that 850/mcg/dose, it is important to note that this amount was selected empirically from data showing that Aluminum in such amounts enhanced the antigenicity of the vaccine, rather than from existing safety. Given that the scientific evidence appears to indicate that vaccine safety is not as firmly established as often believed, it would seem ill advised to exclude paediatric vaccinations as a possible cause of adverse long-term neurodevelopment outcomes, including those associated with autism.

Shaw and Seneff also recently published a paper in the journal Immunome Research outlining a lot of evidence pointing to the dangers regarding aluminum in vaccines.

A paper published in the peer reviewed International Journal of Environmental Research and Public Health titled “Thimerosal Exposure and the Role of Sulfation Chemistry and Thiol Availability in Autism” concluded:

With the rate of children diagnosed with an ASD in the US now exceeding 1 in 50 children and the rate of children with neurodevelopment/behavioural disorders in the US now exceeding 1 in 6 children, and the preceding evidence showing that there is vulnerability to ™ that would not be known without extensive testing, the preponderance of the evidence indicates that ™ should be removed from all vaccines.

A paper published in the journal Entropy draws similar conclusions:

Using standard log-likelihood ratio techniques, we identify several signs and symptoms that are significantly more prevalent in vaccine reports after 2000, including cellulitis, seizure, depression, fatigue, pain and death, which are also significantly associated with aluminum-containing vaccines. We propose that children with the autism diagnosis are especially vulnerable to toxic metals such as aluminum and mercury due to insufficient serum sulfate and glutathione. A strong correlation between autism and the MMR (Measles, Mumps, Rubella) vaccine is also observed, which may be partially explained via an increased sensitivity to acetaminophen administered to control fever.

A paper published in the Journal of Toxicology titled “B-Lymphocytes from a population of Children with Autism Spectrum Disorder and Their Unaffected Siblings Exhibit Hypersensitivity to Thimerosal” clearly demonstrates that certain individuals with a mild mitochondrial defect may be highly susceptible to mitochondrial specific toxins like thimerosal. What does this mean? It means that people with a slight DNA difference are at risk for developing neurodegenerative diseases via vaccination. They determined that ASD patients have a heightened sensitivity to thimerosal which would restrict cell proliferation that is typically found after vaccination.

A study published in the American Journal of Clinical Nutrition determined that an increased vulnerability to oxidative stress and decreased capacity for methylation may contribute to the development and clinical manifestation of autism. It’s well known that viral infections cause increased oxidative stress.  Research suggests that metals, including those found in many vaccines, are directly involved in increasing oxidative stress.

Oxidative stress, brain inflammation, and microgliosis have been heavily documented in association with toxic exposures, including various heavy metals. 

A study published in the Journal of Biomedical Sciences determined that the autoimmunity to the central nervous system may play a causal role in autism. Researchers discovered that because many autistic children harbour elevated levels of measles antibodies, they should conduct a serological study of measles-mumps-rubella (MMR) and myelin basic protein (MBP) autoantibodies. They used serum samples of 125 autistic children and 92 controlled children. Their analysis showed a significant increase in the level of MMR antibodies in autistic children. The study concludes that the autistic children had an inappropriate or abnormal antibody response to MMR, and determined that autism could be the result of an atypical measles infection that produces neurological symptoms in some children. The source of this virus could be a variant of MV, or “it could be the MMR vaccine.”

A study published in the International Journal of Toxicology outlines the biological plausibility of mercury’s role in neurodevelopmental disorders. It suggests that early mercury exposure could indeed increase the risk of autism.

“To sum up, there has been a great deal of information from different studies that seems to indicate that repetitive mercury exposure during pregnancy, through thimerosal, dental amalgam, and fish consumption, and after birth, through thimerosal-containing vaccinations and pollution, in genetically susceptible individuals is one potential factor in autism.” (source)

A study conducted by the Department of Paediatrics at the University of Arkansas determined that thimerosal-induced cytotoxicity was associated with the depletion of intracellular glutathione (GSH) in both cell lines.  The study outlines how many vaccines have been neurotoxic, especially to the developing brain. Depletion of GSH is commonly associated with autism. Although thimerosal has been removed from most children’s vaccines, it is still present in flu vaccines given to pregnant women, the elderly, and children in developing countries.

According to Lucija Tomljenovic, who has a PhD in biochemistry, is a senior postdoctoral fellow in UBC’s Faculty of Medicine, and worked on the above studies with Chris Shaw:

The assertion that vaccine-autism concerns rest merely on spurious claims made by uneducated parents is in stark contrast with a large body of scientific literature. As mentioned previously, extensive research data has underscored the tight connection between development of the immune system and that of the CNS, and thus the plausibility that disruption of critical events in immune development may play a role in neurobehavioral disorders including those of the autism spectrum. Indeed, early-life immune challenges in critical windows of developmental vulnerability have been shown to produce long-lasting, highly abnormal cognitive and behavioral responses, including increased fear and anxiety, impaired social interactions, deficits in object recognition memory and sensorimotor gating deficits. These symptoms are highly characteristic of autism. It is thus indeed naive to assume that a manipulation of the immune system through an increasing number of vaccinations during sensitive periods of early development will not result in adverse neurological outcomes. Consistent with this, Shoenfeld and Cohen (world’s leading experts in autoimmune diseases) noted that, ‘‘vaccines have a predilection to affect the nervous system.’’ Also, please refer to a number of publications we and others have authored on this subject (link between immune challenges and adverse neurological outcomes.)

For more studies, you can refer to these to start off your research.

  1. Gallagher, C.M. and Goodman, M.S. (2010) Hepatitis B vaccination of male neonates and autism diagnosis, NHIS 1997-2002. J Toxicol Environ Health A 73, 1665-77.
  2. Gallagher, C.M. and Goodman, M.S. (2008) Hepatitis B triple series vaccine and developmental disability in US children aged 1-9 years. Tox Env Chem. 90, 997-1008.
  3. Ratajczak, H.V. (2011) Theoretical aspects of autism: causes–a review. J Immunotoxicol 8, 68-79.

The list literally goes on and on. Study after study in peer-reviewed scientific journals claims a possible link between vaccines/vaccine ingredients and autism. 

So, for the “pro-vaccine” community to say there is no link, and can’t be a link, and that vaccines could not be one out of several possible causes contributing to the development of autism, seems a little bit ridiculous, don’t you think?

Concluding Statement About the Vaccine/Autism Controversy

As you can see above, there are many peer-reviewed studies published in scientific journals claiming no link. On the other hand, we have the same type of research, also in abundance, that claims there could be a link, and that it is probable — and through science they’ve shown how.

What are parents who do their research supposed to think when they come across this information? Why is the “pro vac side” so adamant in saying that there are no scientific peer-reviewed published studies that posit a potential link to autism when there are, in fact, many?

So, this is one reason why parents are choosing not to vaccinate their children. To say there is absolutely no way a vaccine can be a contributing factor in causing autism is completely false and dangerous.

#2 Scientific/Industry Fraud

“The medical profession is being bought by the pharmaceutical industry, not only in terms of the practice of medicine, but also in terms of teaching and research. The academic institutions of this country are allowing themselves to be the paid agents of the pharmaceutical industry. I think it’s disgraceful.”  

Arnold Seymour Relman (1923-2014), Harvard Professor of Medicine and former Editor-in-Chief of the New England Medical Journal  (source) 

When a parent points to the idea that scientific and industry fraud contributed to their decision to not vaccine their child, most people are quick to call them conspiracy theorists or outright fools, but this couldn’t be further from the truth, and those types of responses often come from those who have failed to do any investigation for themselves.

“Condemnation without investigation is the height of ignorance.”

Here is why parents are pointing to scientific/industry fraud when it comes to making their decision, and to be honest, with this type of information out in the public domain, who can really blame them?

It’s hard to know where to start when there are so many examples.

In the past few years, more professionals have come forward to share a truth that, for many people, proves difficult to swallow. One such authority is Dr. Richard Horton, the current editor-in-chief of The Lancet — considered one of the most respected peer-reviewed medical journals in the world.

Dr. Horton recently published a statement declaring that a lot of published research is in fact unreliable at best, if not completely false:

The case against science is straightforward: much of the scientific literature, perhaps half, may simply be untrue. Afflicted by studies with small sample sizes, tiny effects, invalid exploratory analyses, and flagrant conflicts of interest, together with an obsession for pursuing fashionable trends of dubious importance, science has taken a turn towards darkness

Lucija Tomljenovic, who has a PhD in biochemistry and is a senior postdoctoral fellow in UBC’s Faculty of Medicine, is also a medical investigator. A few years ago she uncovered documents that reveal vaccine manufacturers, pharmaceutical companies, and health authorities have known about multiple dangers associated with vaccines but chose to withhold them from the public. This is scientific fraud, and this practice continues to this day. The documents were obtained from the UK Department of Health (DH) and the Joint Committee on Vaccination and Immunization (JCVI), who advise the Secretaries of State for Health in the UK about diseases preventable through immunizations. The JCVI made “continuous efforts to withhold critical data on severe adverse reactions and contraindications to vaccinations to both parents and health practitioners in order to reach overall vaccination rates.”

She says:

The transcripts of the JCBI meetings also show that some of the Committee members had extensive ties to pharmaceutical companies and that the JCVI frequently co-operated with vaccine manufactures on the strategies aimed at boosting vaccine uptake. Some of the meetings at which such controversial items were discussed were not intended to be publicly available, as the transcripts were only released later, through the Freedom of Information Act (FOI). These particular meetings are denoted in the transcripts as “commercial in confidence,” and reveal a clear and disturbing lack of transparency, as some of the information was removed from the text (i.e., the names of the participants) prior to transcript release under the FOI section at the JCVI website.

A Congressional Record from May 1, 2003 shows that there could be, and that many scientists themselves believe there to be, a high risk of autism as a result of Thimerosal-containing vaccines. Again, this is a Congressional Report, not a pseudoscientific and unsourced article on the web, and parents who choose not to ignore it should not be bashed by others, don’t you think? The report even shows information from the CDC’s own Vaccine Safety Datalink (VSD) that postulates the vaccine-autism connection.

Insider whistleblowers with verified credentials have also played a role in this debate. Take Robert F. Kennedy Jr, for example. He repeatedly stated that there is a “cover up” of data that clearly shows a definitive link between vaccines and autism. He also revealed that he has met with some of these people, that they know what they are doing, and that they are terrified of the public ever finding out.  Think about that for a second: We have the former president’s nephew, who circulates in elitist circles and obviously connected to people who’ve held powerful positions, making these comments. These are concerning comments, and wanting to learn more isn’t a bad thing. One of the biggest concerns for parents relates to an article he authored in June 2005 for Rolling Stone and Salon.com alleging a government conspiracy to cover up connections between vaccines and autism. Both of the articles were retracted. There are many speeches he made, and compelling statements that are available in the form of articles and YouTube videos, if you are interested in seeing more.

Although a whistleblower is not science, such testimony does add weight to the science that is already there.

We also have statements from scientists and doctors like the one below that also seem to be contributing to a lack of trust for vaccine manufacturers and the studies they sponsor. Most of the published scientific studies that say there is no need to worry about vaccines and that there is no autism link are actually sponsored by the vaccine manufactures themselves.

“It is simply no longer possible to believe much of the clinical research that is published, or to rely on the judgement of trusted physicians or authoritative medical guidelines. I take no pleasure in this conclusion, which I reached slowly and reluctantly over my two decades as an editor of the New England Journal of Medicine.” 

 – Dr. Marcia Angell, physician, author, former Editor in Chief of the New England Journal of Medicine 

A more recent example (and perhaps one of the biggest) is longtime CDC scientist Dr. William Thompson, who has authored and co-authored dozens of studies, many of which are commonly cited by the “pro-vaccine” movement, including a couple referenced above. Yet, just a few months ago, he had this to say“The CDC has put the research 10 years behind, because the CDC has not been transparent. We’ve missed 10 years of research because the CDC is so paralyzed right now by anything related to autism. Really what we need is for congress to come in and say, give us the data.” 

He pointed to a specific study that he co-authored, a 2004 CDC study commonly cited and used by the scientific community, among others, that determined: “The evidence is now convincing that the measles-mumps-rubella vaccine does not cause autism or any particular subtypes of autism spectrum disorder.”

He also mentioned another study published in the Journal of Pediatrics that concluded: “The evidence is now convincing that the measles-mumps-rubella vaccine does not cause autism or any particular subtypes of autism spectrum disorder.” 

This is what he had to say about that study: “It’s the lowest point in my career that I went along with that paper and uh, I went along with this, we didn’t report significant findings. I’m completely ashamed of what I did, I have great shame now that I was complicit and went along with this, I have been a part of the problem.” 

This story was becoming so big across alternative news networks, like CE, that mainstream media outlets like CNN picked up on it as quick as they could and tried to spin the story:

“I regret that my co-authors and I omitted statistically significant information in our 2004 article,” Thompson said in a statement sent to CNN by his lawyer. “I have had many discussions with Dr. Brian Hooker over the last 10 months regarding studies the CDC has carried out regarding vaccines and neurodevelopmental outcomes, including autism spectrum disorders. I share his belief that CDC decision-making and analyses should be transparent.” 

That being said, he also said in an official statement from his lawyers on August 27th 2014: “I want to be absolutely clear that I believe vaccines have saved and continue  to save countless lives. I would never suggest that any parent avoid vaccinating children of any race. Vaccines prevent serious diseases, and the risks associated  with their administration are vastly outweighed  by their individual and societal benefits.” 

This brings me to my next point. With regards to the data omitted above, Dr. Thompson made the call to scientist Dr. Brian Hooker, who published the real findings, which found that there was a 340% increased chance of autism in African American boys receiving the MMR vaccine on time. The study was published in the peer-reviewed journal Translational Neurodegeneration and was retracted a couple of days later. This is why I am linking it here and not with the  studies above.

That being said, Dr. Hooker has published a number of peer-reviewed studies that have appeared in reputable scientific journals, the journal Translational Neurodegeneration being one, where his study provided epidemiological evidence supporting an association between increasing organic-Hg exposure from Thimerosal-containing childhood vaccines and the risk of an ASD diagnosis. Furthermore, an abstract obtained by Hooker shows “increased risk of developmental neurologic impairment after high exposure to thimerosal-containing vaccine in the first month life.”

Here is a video of a ‘pro-vaccine’ Congressman telling us about this case.

Concluding Comments About Scientific/Industry Fraud

As you can see, parents who cite scientific/industry fraud as one of the reasons for not vaccinating their child are right to be concerned. Most vaccine supporters are completely unaware of this information, which is understandable, as it’s not presented in the mainstream.

#3 The National Childhood Vaccine Injury Act 

During the mid-1970s, there was an increased focus on personal health, and more people became concerned about vaccine safety. Several lawsuits were filed against vaccine manufacturers and healthcare providers by people who believed they had been injured by vaccines, and the evidence presented in court was good enough to win.

As a result, this act was developed to protect any pharmaceutical company, doctor, or medical association from any “fault.” It’s not about pointing fingers, as many people really do believe that every vaccine is safe. Instead of suing the vaccine manufacturer directly, parents must ask the government to admit that the vaccine was responsible for their child’s injury, and ask for compensation for the child’s care.

Pharmaceutical companies are exempt from participating in these proceedings, and taxpayers are the ones who pay for all the vaccine related damages, of which there have been many. Below is a great video explaining the process in detail.

This is clearly another contributing factor as to why parents are not vaccinating their children. Many grey areas and shady practices are involved with the legal process when it comes to vaccine induced injury. The children who have been injured by vaccines alone is another cause for concern, which brings me to my next point.

#4 The Ineffectiveness of Some Vaccines and Vaccine Injury

Again, there are dozens upon dozens of vaccines that are out there. Some might be completely safe, harmless, and necessary, and some might not be.

Let’s take a look at Gardasil. There have been several documented cases of injury as a result of the Gardasil vaccine. According to Dr. Chris Shaw, a professor at the University of British Columbia in the Department of Neuroscience, Ophthalmology, and Visual Sciences, “It is a vaccine that’s been highly marketed, the benefits are over-hyped, and the dangers are underestimated.”

Another doctor making noise regarding the HPV vaccine is Dr. Diane Harper.  She helped design and carry out the Phase II and Phase III safety and effectiveness studies to get Gardasil approved, and authored many of the published papers about it. She has been a paid speaker and consultant to Merck. It’s very unusual for a researcher to publicly criticize a medicine or vaccine she helped get approved.

“They created a huge amount of fear in mothers, and appealed to mothers’ sense of duty to get them to get their daughters vaccinated.”

– Dr. Diane Harper (source)

If we are talking about recent research regarding the HPV vaccine, a new review was just published  in the journal Autoimmunity Reviews titled On the relationship between human papilloma virus vaccine and autoimmune disease.” 

The authors of this study came to the same conclusion as Dr. Harper, writing, “The decision to vaccinate with HPV vaccine is a personal decision, not one that must be made for public health. HPV is not a lethal disease in 95% of the infections; and the other 5% are detectable and treatable in the precancerous stage.”

They also listed several conditions in which HPV vaccination is most likely the culprit, having been linked to a variety of autoimmune diseases that include: Multiple sclerosis, Guillain-Barre syndrome, primary ovarian failure, and more. Gardasil has also been linked to a number of deaths.

You can access more information regarding that vaccine in a recent article I wrote:

Merk’s former doctor predicts Gardasil to become one of the greatest medical scandals of all time

Are you going to tell a parent who cites this information as part of the reason they choose not to get this vaccine that they don’t know what they are talking about?

For another example of the literature that’s out there regarding the flu vaccine, a report published in the British Medical Journal shows how “marketing influenza vaccines thus involves marketing influenza as a threat of great proportions.” The paper outlines this theme throughout. It also shows how recorded deaths from influenza declined sharply over the middle of the 20th century, and that this occurred before the great expansion of mass vaccination campaigns at the start of the 21st century.

Are vaccine manufactures marketing vaccines in a completely wrong way?

Another marketing strategy used to push the flu vaccine is the claim by vaccine manufactures that “flu” and “influenza” are the same. The paper outlines how even the ideal influenza vaccine can only deal with a small part of the “flu” because most “flus” appear to have nothing to do with influenza.

Furthermore, a study published in the Journal of Paediatrics found that 85% of newborn infants experienced abnormal elevations of CRP when given multiple vaccines and up to 70% of those given a single vaccine. CRP is a protein found in the blood, and a rise in this protein is a response to inflammation. Overall, 16% of infants were reported to experience vaccine-associated cardiorespiratory events within 48 hours of immunization. (29)

A great example is the fact that poorly tested vaccines have been administered to young children, which explains why there have been large numbers of major adverse reactions from seasonal influenza vaccines. As a result, they were suspended for use in children under five years of age in Australia. (30)

In a series of rapid responses addressing this issue, published in the British Medical Journal and titled “Adverse events following influenza vaccination in Australia-should we be surprised?,” Peter Collignon, the Director of Infectious Diseases and Microbiology at Australian National University, concluded: “There is poor evidence on how well influenza vaccines prevent any influenza complications in children [10] and other age groups. There is good evidence that influenza vaccines study reports cherry pick results and achieve spurious notoriety. Exposing human beings to uncertain effects is a risky business.”

The list goes on and on, and I could cite hundreds of studies both “for” and “against.”

Instances like children in Europe developing narcolepsy after the H1N1 pandemrix vaccine aren’t helping matters. There are so many examples, and no doubt these examples contribute largely to the decisions parents are making.

# 5 Vaccine Ingredients

This topic was touched upon in the studies presented in the first point. There are numerous studies suggesting that current vaccine ingredients are not a cause for concern. At the same time, there are many that point out they should be a cause for concern.

Common vaccine ingredients include:

  • Aluminum gels or salts of aluminum which are added as adjuvants to help the vaccine stimulate a better response. Adjuvants help promote an earlier, more potent response, and more persistent immune response to the vaccine.
  • Antibiotics which are added to some vaccines to prevent the growth of germs (bacteria) during production and storage of the vaccine. No vaccine produced in the United States contains penicillin.
  • Egg protein is found in influenza and yellow fever vaccines, which are prepared using chicken eggs. Ordinarily, persons who are able to eat eggs or egg products safely can receive these vaccines.
  • Formaldehyde is used to inactivate bacterial products for toxoid vaccines, (these are vaccines that use an inactive bacterial toxin to produce immunity.) It is also used to kill unwanted viruses and bacteria that might contaminate the vaccine during production. Most formaldehyde is removed from the vaccine before it is packaged.
  • Monosodium glutamate (MSG) and 2-phenoxy-ethanol which are used as stabilizers in a few vaccines to help the vaccine remain unchanged when the vaccine is exposed to heat, light, acidity, or humidity.
  • Thimerosal is a mercury-containing preservative that is added to vials of vaccine that contain more than one dose to prevent contamination and growth of potentially harmful bacteria

With regards to aluminum, studies (6)(7)(8)(9) are a good place to start if you want to examine the dangers of aluminum as an adjuvant in vaccines.

recent meta-analysis published in the journal Bio Med Research International found:

The studies upon which the CDC relies and over which it exerted some level of control report that there is no increased risk of autism from exposure to organic Hg in vaccines, and some of these studies even reported that exposure to Thimerosal appeared to decrease the risk of autism. These six studies are in sharp contrast to research conducted by independent researchers over the past 75+ years that have consistently found Thimerosal to be harmful. As mentioned in the Introduction section, many studies conducted by independent investigators have found Thimerosal to be associated with neurodevelopmental disorders. Considering that there are many studies conducted by independent researchers which show a relationship between Thimerosal and neurodevelopmental disorders, the results of the six studies examined in this review, particularly those showing the protective effects of Thimerosal, should bring into question the validity of the methodology used in the studies.

Dr. Theresa Deisher, a PhD in Molecular and Cellular Physiology from Stanford University, the first person to discover adult cardiac derived stem cells, determined that residual human fetal DNA fragments in vaccines may be one of the causes of autism in children through vaccination. (31)

Again, significant association between exposure to thimerosal and neurodevelopmental disorders in children including autism, speech disorders, mental retardation, thinking abnormalities and personality disorders has been reported in a number of  studies.  Many have been cited in this article, here are a couple more:

Geier, D.A. and Geier, M.R. (2006) A meta-analysis epidemiological assessment of neurodevelopmental disorders following vaccines administered from 1994 through 2000 in the United States. Neuro Endocrinol Lett 27, 401-13. [127]

Young, H.A., Geier, D.A. and Geier, M.R. (2008) Thimerosal exposure in infants and neurodevelopmental disorders: an assessment of computerized medical records in the Vaccine Safety Datalink. J Neurol Sci 271, 110-8.

There is abundant evidence for both viewpoints and to support either choice a parent decides to make. There is no reason to ridicule one side and praise the other when both are simply doing what they feel is best.

No Safety Assessments Exist (Toxicity Studies) for Vaccine Ingredients

This is another very important point. Aluminum has been being added to vaccines for approximately 90 years, and one disturbing fact that many people still don’t know is that the Food and Drug Administration (FDA) and vaccine manufacturers themselves have not conducted or included appropriate toxicity studies/testing proving the safety of aluminum, or any other ingredients, for that matter. These ingredients have been put into vaccines based on the assumption that they are safe. Yes, you read that correctly. It’s kind of disturbing, isn’t it?

So because vaccines have been viewed as non-toxic substances, the FDA and vaccine manufactures have not conducted appropriate toxicity studies to prove the safety of vaccine ingredients – more specifically, aluminum.

“I have a document from 2002 from the US Food and Drug Administration (FDA)… discussing the assessment of vaccine ingredients… and testing specifically in animal models.

Back then, the FDA stated that the routine toxicity studies in animals with vaccine ingredients have not been conducted because it was assumed that these ingredients are safe. When I read that I was kind of pulling my hairs out [thinking] ‘So, this is your indisputable evidence of safety?’ “

– Dr. Lucija Tomlijenovic, PhD., a post-doctoral fellow at the University of British Columbia, where she works in neurosciences and the Department of Medicine (source)

She also has documents which reveal that vaccine manufacturers, pharmaceutical companies, and health authorities have known about multiple dangers associated with vaccines but chose to withhold them from the public. They show that health authorities and vaccine manufacturers made “continuous efforts to withhold critical data on severe adverse reactions and contraindications to vaccinations to both parents and health practitioners in order to reach overall vaccination rates, which they deemed were necessary for ‘herd immunity.’ ”

If we take a look at the FDA’s website/guidelines, it’s not like this is a secret. The statement above (from Lucija) comes from their 2002 guidelines, which is a fairly recent document, but more than 10 years later, despite all of the studies demonstrating clear cause for concern, very little has changed.

“Until recently, few licensed vaccines have been tested for developmental toxicity in animals prior to their use in humans.” (source)

“Despite their long use as active agents of medicines and fungicides, the safety levels of these substances have never been determined, either for animals or for adult humans—much less for fetuses, newborns, infants, and children.”

– José G. Dórea, professor at the University of Brasillia’s Department of Nutritional Sciences (source)

A growing number of studies have linked the use of aluminum adjuvants to serious autoimmune outcomes in humans.  (source)(source)(source)(source)

The use of this adjuvant has been connected to all kinds of diseases, from autism to brain disease to Alzheimer’s and much more.

“Experimental research . . . clearly shows that aluminum adjuvants have a potential to induce serious immunological disorders in humans.”

–  Dr. Lucija Tomlijenovic (source)

Numerous studies have shown aluminum’s potential to induce toxic effects, and this is clearly established in medical literature, and has been for a long time.

If significant aluminum load exceeds the body’s capacity to get rid of it, it is deposited into various tissues that include bone, brain, liver, heart, spleen, and muscle. Aluminum is found in cigarettes, cosmetics, food, medicines (aspirin), and much much more. It’s in our environment, and we are surrounded by it. This is concerning, because aluminum was not really around until the industrial revolution. Today, it shows up in so many products. And we know, from the work of Richard Flarend, that aluminum is commonly absorbed into the body, into areas it shouldn’t be, and has been found in various urine samples from multiple studies examining this topic — and that’s not just for aluminum in vaccines.

“We increasingly have this compound that was not part of any biochemical process on Earth, that can now only go and do havoc, which is exactly what it does. It causes all kinds of unusual biochemical reactions.”

– Dr. Chris Shaw, a Neuroscientist and professor at the University of British Columbia

Here is a great video by Dr. Christopher Exley, a professor in bioinorganic chemistry at Keele University and an honorary professor at UHI Millennium Institute. He is known as one of the world’s leading experts on aluminum toxicity.

Related CE Article:

MIT Scientist Shows What Can Happen To Children Who Receive Aluminum Containing Vaccines

 # 6 Vaccine Safety Evidence Is Not Rock Solid. One Size Does Not Fit All.

All drugs are associated with some risks and adverse reactions. The “greater good” argument is concerning because causes of permanent neurodevelopmental disabilities and even deaths following vaccination in children (with genetic and other susceptibilities) have been firmly established in scientific literature. (7)(8)

One important point parents often raise is the fact that clinical trials that could address vaccine safety concerns have not been conducted. No studies have been published in peer-reviewed medical journals that examine the health outcomes of vaccinated populations versus unvaccinated populations. This lack can be attributed to the assumption that vaccines are safe, an assumption that clearly contradicts a lot of scientific data. (32)

Even strong supporters of vaccinations within the scientific community have questioned the scientific legitimacy of “one size fits all” vaccination practices.

For example, Gregory Poland, the Editor-in-Chief of the journal Vaccine and co-author of “The age-old struggle against the antivaccinationists” (33), along with fellow researchers, asks whether, “with the advances coming from the new biology of the 21st Century,” it is time to consider how “new genetic and molecular biology information [might] inform vaccinology practices of the future?” They concluded that the “one-size fits all” approach for all vaccines and all persons should be abandoned.

This assumption is also as a result of vaccine trials commonly excluding vulnerable individuals who might be more susceptible to injury via vaccine. As a result, adverse reactions that occur as a result of vaccinations might be very underestimated.

I also wanted to point out that data also demonstrates that over-stimulating the host’s immune system by repeated immunization with immune antigens and/or adjuvants inevitably leads to autoimmunity, even in genetically non-susceptible animals. (34)(35)

Here is a related video explaining why vaccines should not be considered completely safe.

Can you really blame parents, with all of this information out there?

Concluding Comments

The “pro-vaccination” side seems to be all that is offered in the media, at the doctor’s office, in schools, and in most government sponsored studies. I wrote this article t o help shed light on why parents are choosing not to vaccinate their children, as their side of the story is so rarely discussed. There are countless documents and peer-reviewed scientific studies showing adverse events after vaccination and the dangers associated with vaccinations. It appears that the risks associated with them are far greater than what we are being told, and an unnecessary amount of pressure is placed on parents to vaccinate their children.

Some people might ask, “What about the polio vaccine?” and completely ignore all of the relevant information in this article. They might not know that in 1977 Dr. Jonas Salk, the inventor of the Salk polio vaccine, testified with other scientists that 87% of the polio cases which occurred in the U.S. since 1970 were the by-product of the polio vaccine. The Sabin oral polio vaccine (OPV) is the only known cause of polio in the U.S. today. I am not sourcing this particular fact because I want to encourage others to go out and look for themselves. That is the whole point of this article.

After reading this, it’s hard to imagine why a parent would ever ridiculed for choosing not to vaccinate their child. It’s also not even a fraction of the amount of information out there that explores history, more science, fraud, and more. I cannot do your research for you, so I hope I’ve inspired you to do some of your own.

Next time you come across a parent who has chosen not to vaccinate their baby, try not to judge; instead, try to understand where they are coming from.

Sources:

http://www.mdpi.com/1099-4300/14/11/2227

(1) www.sciencedirect.com/science/article/pii/S0264410X14006367

(2) http://www.jpeds.com/article/S0022-3476%2813%2900144-3/abstract

(3) http://www.ncbi.nlm.nih.gov/pubmed/15342825

(4) http://www.ncbi.nlm.nih.gov/pubmed/17168158

(5)http://informahealthcare.com/doi/abs/10.1586/14760584.3.1.19

(6)http://people.csail.mit.edu/seneff/Shaw_et_al_JOT_2014.pdf

(7)http://www.meerwetenoverfreek.nl/images/stories/Tomljenovic_Shaw-CMC-published.pdf

(8)http://autismoava.org/archivos/1-s2.0-S0162013411002212-main.pdf

(9)  http://people.csail.mit.edu/seneff/Shaw_et_al_Immunome_Res_2013.pdf

(10)http://www.mdpi.com/1660-4601/10/8/3771

(11)http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3697751/

(12)http://ajcn.nutrition.org/content/80/6/1611.full

(13)http://vaccinechoicecanada.com/wp-content/documents/VRAN-Abnormal%20Measles-Mumps-Rubella-Antibodies-CNS-Autoimmunity-Children-Autism-Singh-Lin-Newell-Nelson.pdf

(14)http://www.ncbi.nlm.nih.gov/pubmed/12933322

(15)http://www.sciencedirect.com/science/article/pii/S0161813X04001147

(16) http://nsnbc.me/wp-content/uploads/2013/05/BSEM-2011.pdf

(17) http://www.gpo.gov/fdsys/pkg/CREC-2003-05-21/pdf/CREC-2003-05-21-pt1-PgE1011-3.pdf

(18) http://www.cbsnews.com/news/rolling-stone-retracts-autism-article-but-lots-of-junk-journalism-remains/

(19) http://www.salon.com/2011/01/16/dangerous_immunity/

(20) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2964337/

(22) https://www.youtube.com/watch?v=LhpckzxVEoc#t=381

(23) http://informahealthcare.com/doi/abs/10.1586/14760584.3.1.19

(25) http://www.morganverkamp.com/august-27-2014-press-release-statement-of-william-w-thompson-ph-d-regarding-the-2004-article-examining-the-possibility-of-a-relationship-between-mmr-vaccine-and-autism/

(26) http://web.archive.org/web/20140826171415/http://www.translationalneurodegeneration.com/content/pdf/2047-9158-3-16.pdf

(27) http://www.ncbi.nlm.nih.gov/pubmed/24354891

(28) http://www.bmj.com/content/346/bmj.f3037

(29) http://www.ncbi.nlm.nih.gov/pubmed/17643770

(30) http://www.bmj.com/rapid-response/2011/11/02/adverse-events-following-influenza-vaccination-australia-should-we-be-surp

(31) http://s3.amazonaws.com/soundchoice/soundchoice/wp-content/uploads/2012/08/DNA_Contaminants_in_Vaccines_Can_Integrate_Into_Childrens_Genes.pdf

(32) Tomljenovic, L. and Shaw, C.A. (2011) One-size fits all? Vaccine. 2012; 30(12):2040.9

http://www.vaxchoicevt.com/wp-content/uploads/2012/04/Lucija-Tomljenovic-PhD-letter.pdf

(33) http://www.nejm.org/doi/full/10.1056/NEJMp1010594

(34) http://www.jimmunol.org/cgi/content/meeting_abstract/184/1_MeetingAbstracts/93.39

(35) http://www.ncbi.nlm.nih.gov/pubmed/20353969

Help Support Collective Evolution

The demand for Collective Evolution's content is bigger than ever, except ad agencies and social media keep cutting our revenues. This is making it hard for us to continue.

In order to stay truly independent, we need your help. We are not going to put up paywalls on this website, as we want to get our info out far and wide. For as little as $3 a month, you can help keep CE alive!

SUPPORT CE HERE!

cards

Advertisement
advertisement - learn more

Awareness

Long-Term Consequences of Mumps Vaccination: Many Unanswered Questions

Published

on

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.

advertisement - learn more

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.


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.

Help Support Collective Evolution

The demand for Collective Evolution's content is bigger than ever, except ad agencies and social media keep cutting our revenues. This is making it hard for us to continue.

In order to stay truly independent, we need your help. We are not going to put up paywalls on this website, as we want to get our info out far and wide. For as little as $3 a month, you can help keep CE alive!

SUPPORT CE HERE!

cards

Continue Reading

Alternative News

Legal Challenge Against Forced Vaccination Filed in New York City

Published

on

On April 15, 2019, a legal challenge was filed in the New York State Trial Court by Robert Krakow, Robert F. Kennedy, Jr. and Patricia Finn against the New York City Department of Health and Human Hygiene for their forced Measles-Mumps-Rubella vaccination. The legal team asked for a temporary restraining order against the mandate that the Judge will likely review and provide an ex parte decision. Children’s Health Defense is supporting these efforts.

Last week, Children’s Health Defense reported that the NYC Commissioner of Health declared a public health emergency, ordering all people who live, work or reside in four Brooklyn zip codes to be vaccinated with the Measles-Mumps-Rubella vaccine. Non-compliance with the order is a misdemeanor subject to criminal and civil fines, including imprisonment. Only those with documented immunity, medical contraindications or infants under six months are exempt from the vaccine mandate.

READ THE PETITION
READ THE MEMORANDUM OF LAW
READ THE AFFIRMATION

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.

advertisement - learn more

Help Support Collective Evolution

The demand for Collective Evolution's content is bigger than ever, except ad agencies and social media keep cutting our revenues. This is making it hard for us to continue.

In order to stay truly independent, we need your help. We are not going to put up paywalls on this website, as we want to get our info out far and wide. For as little as $3 a month, you can help keep CE alive!

SUPPORT CE HERE!

cards

Continue Reading

Awareness

Magnesium Puts Psychiatric Drugs to Shame for Depression

Published

on

In Brief

  • The Facts:

    This article was written by Sayer Ji, Founder of Greenmedinfo.com where this article first appeared. Posted here with permission.

  • Reflect On:

    Is the priority of our federal health regulatory agencies and pharmaceutical companies human health, or profit? If there are more effective ways to treat several illnesses, why do they never mention them?

Depression is one of the most widely diagnosed conditions of our time, with over 3 million cases in the U.S. every year, and 350 million believed affected worldwide.1 Conventional medicine considers antidepressant drugs first-line treatments, including the newly approved injected postpartum drug costing $34,000 a treatment, to the tune of a 16 billion dollars in global sales by 2023. Despite their widespread use, these drugs are fraught with a battery of serious side effects, including suicidal ideation and completion — the last two things you would hope to see in a condition that already has suicidality as a co-morbidity. For this reason alone, natural, safe, and effective alternatives are needed more than ever before.

While research into natural alternatives for depression is growing daily — GreenMedInfo.com’s Depression database contains 647 studies on over 100 natural substances that have been studied to prevent or treat depression — it is rare to find quality human clinical research on the topic published in well-respected journals. That’s why a powerful study published in PLOS One titled, “Role of magnesium supplementation in the treatment of depression: A randomized clinical trial,” is so promising. Not only is magnesium safe, affordable, and easily accessible, but according to this recent study, effective in treating mild-to moderate symptoms of depression.

While previous studies have looked at the association between magnesium and depression,2-7 this is the first placebo-controlled clinical study to evaluate whether the use of over-the-counter magnesium chloride (248 mg elemental magnesium a day for 6 weeks) improves symptoms of depression.

The study design was a follows:

“ An open-label, blocked, randomized, cross-over trial was carried out in outpatient primary care clinics on 126 adults (mean age 52; 38% male) diagnosed with and currently experiencing mild-to-moderate symptoms with Patient Health Questionnaire-9 (PHQ-9) scores of 5–19. The intervention was 6 weeks of active treatment (248 mg of elemental magnesium per day) compared to 6 weeks of control (no treatment). Assessments of depression symptoms were completed at bi-weekly phone calls. The primary outcome was the net difference in the change in depression symptoms from baseline to the end of each treatment period. Secondary outcomes included changes in anxiety symptoms as well as adherence to the supplement regimen, appearance of adverse effects, and intention to use magnesium supplements in the future. Between June 2015 and May 2016, 112 participants provided analyzable data.”

The study results were as follows:

advertisement - learn more

“Consumption of magnesium chloride for 6 weeks resulted in a clinically significant net improvement in PHQ-9 scores of -6.0 points (CI -7.9, -4.2; P<0.001) and net improvement in Generalized Anxiety Disorders-7 scores of -4.5 points (CI -6.6, -2.4; P<0.001). Average adherence was 83% by pill count. The supplements were well tolerated and 61% of participants reported they would use magnesium in the future. Similar effects were observed regardless of age, gender, baseline severity of depression, baseline magnesium level, or use of antidepressant treatments. Effects were observed within two weeks. Magnesium is effective for mild-to-moderate depression in adults. It works quickly and is well tolerated without the need for close monitoring for toxicity.”

 For perspective, conventional antidepressant drugs are considering to generate an “adequate or complete treatment response” with a PHQ-9 score “decrease of 5 points or more from baseline.” At this level of efficacy, their recommended action is: “Do not change treatment; conduct periodic follow-up.” The magnesium’s score of -6.0 therefore represents the height of success within conventional expectations for a complete response, which is sometimes termed “remission.” In contradistinction, conventional antidepressant drugs result in nearly half of patients discontinuing treatment during the first month, usually due to their powerful and sometimes debilitating side effects.8

To summarize the main study outcomes:

  • There was a clinically significant improvement in both Depression and Anxiety scores.
  • 61% of patients reported they would use magnesium in the future.
  • Similar effects occurred across age, gender, severity of depression, baseline magnesium levels, or use of antidepressant treatments.
  • Effects were observed within two weeks.

 The study authors concluded:

“Magnesium is effective for mild-to-moderate depression in adults. It works quickly and is well tolerated without the need for close monitoring for toxicity.”

Beyond Depression: Magnesium’s Many Health Benefits & Where To Source It

Magnesium is a central player in your body’s energy production, as its found within 300 enzymes in the human body, including within the biologically active form of ATP known as MG-ATP. In fact, there have been over 3,751 magnesium binding sites identified within human proteins, indicating that it’s central nutritional importance has been greatly underappreciated.

Research relevant to magnesium has been accumulating for the past 40 years at a steady rate of approximately 2,000 new studies a year. Our database project has indexed well over 100 health benefits of magnesium thus far.  For the sake of brevity, we will address seven key therapeutic applications for magnesium as follows:

  • Fibromyalgia: Not only is magnesium deficiency common in those diagnosed with fibromyalgia, 9,10 but relatively low doses of magnesium (50 mg), combined with malic acid in the form of magnesium malate, has been clinically demonstrated to improve pain and tenderness in those to which it was administered.11
  • Atrial Fibrillation: A number of studies now exist showing that magnesium supplementation reduce atrial fibrillation, either by itself, or in combination with conventional drug agents.12
  • Diabetes, Type 2: Magnesium deficiency is common in type 2 diabetics, at an incidence of 13.5 to 47.7% according to a 2007 study. 13 Research has also shown that type 2 diabetics with peripheral neuropathy and coronary artery disease have lower intracellular magnesium levels. 14 Oral magnesium supplementation has been shown to reduce plasma fasting glucose and raising HDL cholesterol in patients with type 2 diabetes.15 It has also been shown to improve insulin sensitivity and metabolic control in type 2 diabetic subjects.16
  • Premenstrual Syndrome: Magnesium deficiency has been observed in women affected by premenstrual syndrome.17 It is no surprise therefore  that it has been found to alleviate premenstrual symptoms of fluid retention, 18 as well as broadly reducing associated symptoms by approximately 34% in women, aged 18-45, given 250 mg tablets for a 3-month observational period.20 When combined with B6, magnesium supplementation has been found to improve anxiety-related premenstrual symptoms.19
  • Cardiovascular Disease and Mortality: Low serum magnesium concentrations predict cardiovascular and all-cause mortality.21 There are a wide range of ways that magnesium may confer its protective effects. It may act like a calcium channel blocker,22it is hypotensive,23 it is antispasmodic (which may protect against coronary artery spasm),24 and anti-thrombotic.25 Also, the heart muscle cells are exceedingly dense in mitochondria (as high as 100 times more per cell than skeletal muscle), the “powerhouses” of the cell,” which require adequate magnesium to produce ATP via the citric acid cycle.
  • Migraine Disorders: Blood magnesium levels have been found to be significantly lower in those who suffer from migraine attacks.26,27 A recent Journal of Neural Transmission article titled, “Why all migraine patients should be treated with magnesium,” pointed out that routine blood tests do not accurately convey the true body magnesium stores since less than 2% is in the measurable, extracellular space, “67% is in the bone and 31% is located intracellularly.”28The authors argued that since “routine blood tests are not indicative of magnesium status, empiric treatment with at least oral magnesium is warranted in all migraine sufferers.” Indeed, oral magnesium supplementation has been found to reduce the number of headache days in children experiencing frequent migranous headaches,29and when combined with l-carnitine, is effective at reducing migraine frequency in adults, as well.30
  • Aging: While natural aging is a healthy process, accelerated aging has been noted to be a feature of magnesium deficiency,31especially evident in the context of long space-flight missions where low magnesium levels are associated with cardiovascular aging over 10 times faster than occurs on earth.32 Magnesium supplementation has been shown to reverse age-related neuroendocrine and sleep EEG changes in humans.33 One of the possible mechanisms behind magnesium deficiency associated aging is that magnesium is needed to stabilize DNA and promotes DNA replication. It is also involved in healing up of the ends of the chromosomes after they are divided in mitosis.34

 It is quite amazing to consider the afformentioned side benefits of magnesium consumption or supplementation within the context of the well-known side effects of pharmaceutical approaches to symptom

management of disease. On average, conventional drugs have 75 side effects associated with their use, including lethal ones (albeit sometimes rare). When considering magnesium’s many side benefits

and extremely low toxicity, clearly this fundamental mineral intervention (and dietary requirement) puts pharmaceutical approaches to depression to shame.

Best Sources of Magnesium In The Diet

The best source of magnesium is from food, and one way to identify magnesium-containing foods are those which are green, i.e. chlorophyll rich. Chlorophyll, which enable plants to capture solar energy and convert it into metabolic energy, has a magnesium atom at its center. Without magnesium, in fact, plants could not utilize the sun’s light energy.

Magnesium, however, in its elemental form is colorless, and many foods that are not green contain it as well. The point is that when found complexed with food cofactors, it is absorbed and utilized more efficiently than in its elemental form, say, extracted from limestone in the form of magnesium oxide.

 The following foods contain exceptionally high amounts of magnesium. The portions described are 100 grams, or a little over three ounces.

  • Rice bran, crude (781 mg)
  • Seaweed, agar, dried (770 mg)
  • Chives, freeze-dried (640 mg)
  • Spice, coriander leaf, dried (694 mg)
  • Seeds, pumpkin, dried (535 mg)
  • Cocoa, dry powder, unsweetened (499 mg)
  • Spices, basil, dried (422 mg)
  • Seeds, flaxseed (392 mg)
  • Spices, cumin seed (366 mg)
  • Nuts, brazilnuts, dried (376 mg)
  • Parsley, freeze-dried (372 mg)
  • Seeds, sesame meal (346 mg)
  • Nut, almond butter (303 mg)
  • Nuts, cashew nuts, roasted (273 mg)
  • Soy flour, defatted (290 mg)
  • Whey, sweet, dried (176 mg)
  • Bananas, dehydrated (108 mg)
  • Millet, puffed (106 mg)
  • Shallots, freeze-dried (104 mg)
  • Leeks, freeze-dried (156 mg)
  • Fish, salmon, raw (95 mg)
  • Onions, dehydrated flakes (92 mg)
  • Kale, scotch, raw (88 mg)

 Fortunately, for those who need higher doses, or are not inclined to consume magnesium rich foods, there are supplemental forms commonly available on the market. Keep in mind, for those who wish to take advantage of the side benefit of magnesium therapy, namely, its stool softening and laxative properties, magnesium citrate or oxide will provide this additional feature.

For those looking to maximize absorption and bioavailability magnesium glycinate is ideal, as glycine is the smallest amino acid commonly found chelated to magnesium, and therefore highly absorbable.

For more information on natural solutions to resolving depression, download our free e-book on the topic “21st Century Solutions to Depression.” 

References:

1) World Health Organization. Depression fact sheet no. 369 2012 [cited 2016 December 20]. Available from: http://www.who.int/mediacentre/factsheets/fs369/en/.

2) Jacka FN, Overland S, Stewart R, Tell GS, Bjelland I, Mykletun A. Association between magnesium intake and depression and anxiety in community-dwelling adults: the Hordaland Health Study. Aust N Z J Psychiatry. 2009;43(1):45–52. Pmid:19085527.

3) Huang JH, Lu YF, Cheng FC, Lee JN, Tsai LC. Correlation of magnesium intake with metabolic parameters, depression and physical activity in elderly type 2 diabetes patients: a cross-sectional study. Nutrition J. 2012;11(1):41. pmid:22695027; PubMed Central PMCID: PMC3439347.

4) Tarleton EK, Littenberg B. Magnesium intake and depression in adults. J Am Board Fam Med. 2015;28(2):249–56. Pmid:25748766

5) Yary T, Lehto SM, Tolmunen T, Tuomainen T-P, Kauhanen J, Voutilainen S, et al. Dietary magnesium intake and the incidence of depression: a 20-year follow-up study. J Affect Disord. 2016;193:94–8. Pmid:26771950

6) Eby GA, Eby KL. Rapid recovery from major depression using magnesium treatment. Med Hypotheses. 2006;67(2):362–70. pmid:16542786

7) N Engl J Med. 2000 Dec 28;343(26):1942-50. Managing depression in medical outpatients.

8)  Damiano Piovesan, Giuseppe Profiti, Pier Luigi Martelli, Rita Casadio. 3,751 magnesium binding sites have been detected on human proteins. BMC Bioinformatics. 2012 ;13 Suppl 14:S10. Epub 2012 Sep 7. PMID: 23095498

9) G Moorkens, B Manuel y Keenoy, J Vertommen, S Meludu, M Noe, I De Leeuw. Magnesium deficit in a sample of the Belgian population presenting with chronic fatigue. Magnes Res. 1997 Dec;10(4):329-37. PMID: 9513929

10)  J Eisinger, A Plantamura, P A Marie, T Ayavou. Selenium and magnesium status in fibromyalgia. Magnes Res. 1994 Dec;7(3-4):285-8. PMID: 7786692

11)  I J Russell, J E Michalek, J D Flechas, G E Abraham. Treatment of fibromyalgia syndrome with Super Malic: a randomized, double blind, placebo controlled, crossover pilot study. J Rheumatol. 1995 May;22(5):953-8. PMID: 8587088

12) GreenMedInfo.com, Atrial Fibrillation and Magnesium (5 studies)

13)  Phuong-Chi T Pham, Phuong-Mai T Pham, Son V Pham, Jeffrey M Miller, Phuong-Thu T Pham . Hypomagnesemia in patients with type 2 diabetes. Clin J Am Soc Nephrol. 2007 Mar;2(2):366-73. Epub 2007 Jan 3. PMID: 17699436

14)  M de Lordes Lima, T Cruz, J C Pousada, L E Rodrigues, K Barbosa, V Canguçu. The effect of magnesium supplementation in increasing doses on the control of type 2 diabetes. Diabetes Care. 1998 May;21(5):682-6. PMID: 9589224

15) Y Song, K He, E B Levitan, J E Manson, S Liu. Effects of oral magnesium supplementation on glycaemic control in Type 2 diabetes: a meta-analysis of randomized double-blind controlled trials. Cardiovasc Toxicol. 2008;8(3):115-25. Epub 2008 Jul 8. PMID: 16978367

16)  Martha Rodríguez-Morán, Fernando Guerrero-Romero. Oral magnesium supplementation improves insulin sensitivity and metabolic control in type 2 diabetic subjects: a randomized double-blind controlled trial. Diabetes Care. 2003 Apr;26(4):1147-52. PMID: 12663588

17)  F Facchinetti, P Borella, G Sances, L Fioroni, R E Nappi, A R Genazzani. Oral magnesium successfully relieves premenstrual mood changes. Obstet Gynecol. 1991 Aug;78(2):177-81. PMID: 2067759

18)  A F Walker, M C De Souza, M F Vickers, S Abeyasekera, M L Collins, L A Trinca. Magnesium supplementation alleviates premenstrual symptoms of fluid retention. J Womens Health. 1998 Nov;7(9):1157-65. PMID: 9861593

19)  S Quaranta, M A Buscaglia, M G Meroni, E Colombo, S Cella. Pilot study of the efficacy and safety of a modified-release magnesium 250 mg tablet (Sincromag) for the treatment of premenstrual syndrome. Am J Gastroenterol. 2008 Dec;103(12):2972-6. PMID: 17177579

20) M C De Souza, A F Walker, P A Robinson, K Bolland. A synergistic effect of a daily supplement for 1 month of 200 mg magnesium plus 50 mg vitamin B6 for the relief of anxiety-related premenstrual symptoms: a randomized, double-blind, crossover study. J Womens Health Gend Based Med. 2000 Mar;9(2):131-9. PMID: 10746516

21) Thorsten Reffelmann, Till Ittermann, Marcus Dörr, Henry Völzke, Markus Reinthaler, Astrid Petersmann, Stephan B Felix. Low serum magnesium concentrations predict cardiovascular and all-cause mortality. Atherosclerosis. 2011 Jun 12. Epub 2011 Jun 12. PMID: 21703623

22) Andrea Rosanoff, Mildred S Seelig. Comparison of mechanism and functional effects of magnesium and statin pharmaceuticals. J Am Coll Nutr. 2004 Oct;23(5):501S-505S. PMID: 15466951

23)  GreenMedInfo.com, Magnesium’s Hypotensive Properties.

24) GreenMedInfo.com, Magnesium’s Antispasmodic Properties.

25) Joen R Sheu, George Hsiao, Ming Y Shen, Yen M Lee, Mao H Yen . Antithrombotic effects of magnesium sulfate in in vivo experiments. Int J Hematol. 2003 May;77(4):414-9. PMID: 12774935

26) Afshin Samaie, Nabiollah Asghari, Raheb Ghorbani, Jafar Arda. Blood Magnesium levels in migraineurs within and between the headache attacks: a case control study. Pan Afr Med J. 2012 ;11:46. Epub 2012 Mar 15. PMID: 22593782

27) Mahnaz Talebi, Dariush Savadi-Oskouei, Mehdi Farhoudi, Solmaz Mohammadzade, Seyyedjamal Ghaemmaghamihezaveh, Akbar Hasani, Amir Hamdi. Relation between serum magnesium level and migraine attacks. Neurosciences (Riyadh). 2011 Oct ;16(4):320-3. PMID: 21983373

28) Alexander Mauskop, Jasmine Varughese. Why all migraine patients should be treated with magnesium. J Neural Transm. 2012 May ;119(5):575-9. Epub 2012 Mar 18. PMID: 22426836

29)  Fong Wang, Stephen K Van Den Eeden, Lynn M Ackerson, Susan E Salk, Robyn H Reince, Ronald J Elin. Oral magnesium oxide prophylaxis of frequent migrainous headache in children: a randomized, double-blind, placebo-controlled trial. Eur J Endocrinol. 2009 Apr;160(4):611-7. Epub 2009 Jan 29. PMID: 12786918

30) Ali Tarighat Esfanjani, Reza Mahdavi, Mehrangiz Ebrahimi Mameghani, Mahnaz Talebi, Zeinab Nikniaz, Abdolrasool Safaiyan. The effects of magnesium, L-carnitine, and concurrent magnesium-L-carnitine supplementation in migraine prophylaxis. Biol Trace Elem Res. 2012 Dec ;150(1-3):42-8. Epub 2012 Aug 17. PMID: 22895810

31) David W Killilea, Jeanette A M Maier. A connection between magnesium deficiency and aging: new insights from cellular studies. Magnes Res. 2008 Jun;21(2):77-82. PMID: 18705534

32) GreenMedInfo.com, What We Learned From The Accelerated Aging of Astronauts

33) Katja Held, I A Antonijevic, H Künzel, M Uhr, T C Wetter, I C Golly, A Steiger, H Murck. Oral Mg(2+) supplementation reverses age-related neuroendocrine and sleep EEG changes in humans. Pharmacopsychiatry. 2002 Jul;35(4):135-43. PMID: 12163983

34) William J Rowe. Correcting magnesium deficiencies may prolong life. Clin Interv Aging. 2012 ;7:51-4. Epub 2012 Feb 16. PMID: 22379366


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.


For more info from Greenmedinfo, you can join their newsletter by clicking here.


Link to original article. 

Help Support Collective Evolution

The demand for Collective Evolution's content is bigger than ever, except ad agencies and social media keep cutting our revenues. This is making it hard for us to continue.

In order to stay truly independent, we need your help. We are not going to put up paywalls on this website, as we want to get our info out far and wide. For as little as $3 a month, you can help keep CE alive!

SUPPORT CE HERE!

cards

Continue Reading
advertisement - learn more
advertisement - learn more

Video

Pod