The Dangers Of Vaccines and Vaccination
Vaccination is a medical treatment administered to an otherwise healthy individual. Virtually all other invasive medical interventions occur only once someone has fallen ill. Vaccination, like most medical treatments, can involve some risk. And therefore it should be undertaken only after careful consideration of its risks versus its benefits.
The dangers of vaccines are real, can be substantial and life-long, and for some, life ending. Additionally vaccines:
have not been subject to toxicity studies for many of the ingredients such as aluminum and mercury, which are known neurotoxins
have not been studied for adverse effects in the combinations in which they’re given (multiple shots in a single day for infants and children)
cannot be guaranteed to provide the benefit of immunity for which they are given
are used to “prevent” benign childhood diseases, diseases which actually “teach” the immune system how to work properly
Vaccines are “unavoidably unsafe” and contain “unavoidable” viruses, phages (viruses that infect bacteria), and contaminants. No other drug or medical product is similarly manufactured – if contaminants are found in them, the product is recalled. The FDA even recalls food when contaminants are found.
Some of the viruses contaminating vaccines have a known effect, as in the case of the simian virus SV-40 that causes cancer (see Cross-Species Contamination below). Other effects are unknown. In 1975 Gena Bari Kolata wrote an article[i] in the journal Science in which scientists at the FDA admit that all live virus vaccines are “grossly contaminated with phages,” even though it was against FDA regulations at that time. Rather than recall the vaccines, the FDA changed the rules so that a recall wouldn’t cause undue concern for parents. In 1987 the FDA decided this about vaccines: “seed virus used in manufacture shall be demonstrated to be free of extraneous microbial agents except for unavoidable bacteriophage.”[ii] Bovine (cow) serum is a frequently used vaccine growth medium and the most frequently contaminated animal serums with bacteriophage.
Vaccines have many other agents as well as the viruses and contaminants that can cause significant injury (see the full list below) to a child or adult. These injuries include brain swelling and permanent brain injury, seizures and convulsions, blood disorders, and even death. Since 1988 over 3.4 billion dollars in compensation has been paid by the federal government to vaccine victims. And yes, they have paid for autism. Studies have definitively shown that vaccines can result in autism, a disease that has increased from 1 in 10,000 in 1990, to 1 in 150 in 2000, to the current rate of 1 in 68 children. According to the CDC, the most recent numbers breakdown to 1 in 42 boys and 1 in 189 girls diagnosed with autism.
While other environmental assaults are also associated with autism, the increased vaccination schedule can be the trigger or a significant contributing factor especially in children who are predisposed because of other conditions. These other conditions are often unknown and not symptomatic until the vaccine injury triggers a cascade of problems.
Vaccines Are Unavoidably Unsafe
According to the US Food and Drug Administration, safety assessments for vaccines have not often included toxicity studies because vaccines have not been viewed as inherently toxic. Yet vaccines are legally defined as unavoidably unsafe.
It is not just childhood vaccines that come with substantial risk. Influenza vaccines, vaccines for sexually transmitted diseases, and others contain similar risks for adverse events. Also troubling is that vaccination is recommended now for pregnant women, even though vaccine package inserts clearly state they have not been tested on pregnant women, so the effects on the fetus can’t be known.
In the 1960s only a handful of childhood vaccines were given. The current CDC recommended vaccine schedule for children now has over 30 vaccines by the time a child turns 6 and an additional potential for up to 30 more by the time they reach 18. Could this increase be linked to our declining health? For example, currently:
One in six children in the US has a learning disability
Over 50% suffer from some type of chronic illness.
Cancer is the leading cause of death in our children
Autism rates have soared from 1 in 10,000 in 1990 to 1 in 68 today
Since genetic mutations change slowly over generations, we must look to environmental causes for these changes. While other environmental toxins certainly are at play in these statistics, disregarding the potential role to the amounts of toxin injected into children through vaccines is not only bad public policy, it is bad science. By disregarding the role of vaccines in our statistics for infant mortality and chronic diseases, we could be doing more harm than good in mandating, or even advising, them.
Vaccine Adverse Effects: Known Risks
The list of adverse side effects for vaccines is long and troubling. A quick scan of the Vaccine Injury Table kept by the Health Resource Center for the U.S. Department of Health and Human Services reveals that compensation for injury is possible from a variety of the most common vaccines given to children.
Adverse events are the reason the Vaccine Injury Compensation Program has paid out over 3 billion dollarsfrom 1988 – 2016 despite the fact that only 1 in 5 claims receives any compensation at all. Studies reveal that a small fraction of those injured by vaccines ever file any claim at all since most doctors reject the notion that a problem was caused by a vaccine despite the reality that such problems are listed on the manufacturers product insert. You can learn more by reading this fficial document: National Vaccine Injury Compensation Program.
Vaccines: Adverse Effects List
Various vaccines are linked to the following serious adverse reactions:
Aseptic meningitis, meningitis
Bell’s palsy, facial palsy, isolated cranial nerve palsy
Blood disorders such as thrombocytopenic purpura (a disease that destroys platelets need for clotting)
Cerebrovascular accident (stroke)
Chronic rheumatoid arthritis
Convulsions, seizures, febrile seizure
Encephalopathy and encephalitis (brain swelling)
Immune system disorders
Lymphatic system disorders
Nervous system disorders
Neurological syndromes including autism
Paralysis and myelitis including transverse myelitis
Pneumonia and lower respiratory infections
Skin and tissue disorders including eczema
Sudden infant death syndrome (SIDS)
Tinnitus (ringing in the ears)
Vaccine-strain versions of chicken pox, measles, mumps, polio, influenza, meningitis, yellow fever, and pertussis
Vasculitis (inflammation of blood vessels)
You can find more adverse reactions reported on the Vaccine Adverse Events Reporting System (VAERS) database.
Mitochondrial Dysfunction and Vaccines
People have varied genetic makeup and individual responses so there isn’t a way to tell if a given vaccine will provide the benefit of immunity, cause the illness it’s meant to prevent, or cause mild and/or serious neurologic illness or other “adverse events” (including death) following vaccination in some individuals.
Vaccines are known to be problematic for a segment of the population with a specific mitochondrial genetic mutation which may affect up to 4,000 babies a year. Some of those with a particular form of this dysfunction are unable to detoxify the poisons such as aluminum or mercury that are in the vaccine. This inability to detoxify the metals causes damage to multiple organ systems with sometimes devastating results.
In his 2004 testimony to Congress, Dr. Rashid Buttar [iv] (former vice chair of the American Board of Clinical Metal Toxicology and scientist at North Carolina State University) said that children with autism suffer from acute mercury toxicity which results in many imbalances, including systemic candidiastis, immune-suppression, immune dysfunctions, and gastrointestinal dysbiosis. He calls these conditions fires which resulted from one spark: mercury, including (and exacerbated by) the mercury in trace amounts still in childhood vaccines.
Inadequate Testing of Vaccines
The problems associated with vaccines should lead manufacturers to conduct stringent testing. However, quite the opposite is true. In vaccine testing there is:
No cumulative safety testing done prior to licensing
No placebo standard safety testing done
No carcinogenic or mutagenic capacity testing done (even though vaccines contain animal DNA and carcinogens)
No route of exposure research to determine effective safe limits of ingredients
Safety or toxicity of vaccines is studied for short term rather than long-term. Many studies are limited to just a few weeks. When a vaccine is tested, it is given to healthy people and they are only given that one injection (not multiple injections at once, like a baby). The current CDC recommended schedule with a number of vaccines injected on a given day has never been tested. In essence, the current schedule is an experiment.
Vaccines Introduced 1985-1991 Were Not Studied For Autism
Chronic health conditions in children began growing rapidly at the same time that new vaccines were introduced 1985-1991, now impacting 1 in 2 adolescents. Autism, ADHD, food allergies, bowel diseases, and other conditions began growing exponentially in the late 1980s.
The Hib vaccine was introduced in 1985, and replaced by the Hib conjugate vaccine in 1988, to avoid a death rate of 1 per 106,000 persons. The Hepatitis B vaccine was introduced for newborns in 1991 to avoid the risk of transmission from the mother which can occur in 1 in 480 births. HepB is a blood-borne illness not transmitted by casual contact, so an infant is not at risk unless the mother is HepB-positive. Learn more by reading the report created by Foundation for Pediatric Health.
Vaccine Additives: Mercury, and Aluminum
One traditional rule in medicine is that things are unsafe until proven otherwise. Despite this, and the understanding that aluminum is a neurotoxin, scientists still don’t understand exactly what aluminum does in the vaccine.
According to a 2007 article entitled “Neurological Adverse Events of Immunization: Experience With an Aluminum Adjuvanted Meningococcal B Outer Membrane Vesicle Vaccine” on MedScape, “aluminum salts (aluminum hydroxide, aluminum phosphate and alum) have been the main adjuvants used in vaccines for almost 80 years and are the only adjuvants currently licensed for use in humans in the USA. Despite the long experience, the mechanism of action still appears unclear. For many years, the main effect of alum was believed to be keeping the active antigen at the injection site and, therefore, available for initial interaction with the immune system. However, experimental studies have shown that the antigen disappears from the injection site within a few hours. The most important mechanism of alum is probably mediated through activation of antigen-presenting cells. Aluminum adjuvants also strongly influence the type of immune response and are important for stimulation of antibody production but probably do not induce cell-mediated immunity.”
Two things stand out: researchers are not sure what aluminum adjuvants do exactly but they guess that whatever action is relevant does not include cell-mediated immunity. Cell-mediated immunity creates actual immunity; antibody production alone does not.
This particular paper goes on to describe many adverse effects of the aluminum adjuvant, including serious neurological dysfunction, but the authors insist that most of the adverse effects are coincidental and not causal. Even when the authors admit to vaccine-induced adverse events, they say that the vaccine is still better for most people than the life-long problems experienced by those injured.
This paper also notes that in developing new adjuvants for vaccines “In-depth studies demonstrating the overall effect of the adjuvants on the immune system will be necessary to avoid surprising and negative consequences … However, should there be the more serious events occurring in less than one in 10,000 vaccines, they will only be revealed when the vaccine is taken into general use.” In other words, the general population is the completion of their experiment for safety.
Mercury, another heavy metal and known neurotoxin, is in all inactivated flu vaccines where it is used as a preservative in the form of thimerosal. Though thimerosal is no longer used as a preservative in childhood vaccines, it remains present in them in in trace amounts since it is part of the manufacturing process. However, those trace amounts still exceeds the FDA recommended amounts that can be ingested. Vaccines are injected rather than ingested. So is there a safe amount to inject? We don’t know because that research has never been done. The FDA ordered such studies in 1982; the CDC still has not commissioned such a study.
Mercury, even in small trace amounts, is harmful. Exposure to any mercury is problematic because like aluminum, it also accumulates in the brain causing many forms of neurological damage that affects movement, learning, and social behaviors. Mercury is 500 times more toxic than lead and is second only to plutonium as the most toxic metal known to man. Mercury poisoning and the symptoms of autism are strikingly similar.
Since it takes years for mercury to be metabolized out of the body, its effects are also cumulative. Mercury is especially harmful to fetuses, infants, and young children since their brains are still developing.
One final problem with mercury is that combining it with other metals, such as aluminum, exponentiallyincreases its toxicity. In one recent study done at the University of British Columbia, researchers placed brain neurons in a dish and video recorded the reaction of the neurons when adding aluminum and mercury in the amounts that corresponded to vaccines. When the researchers added aluminum to the brain cells, the neurons withered and shrunk noticeably. When they then added mercury to the aluminum damaged cell, the destruction continued and was more rapid and intense. When they then added testosterone to the mercury/aluminum mixture, the destruction of the neural cell was profound.
Vaccine Ingredients, How They’re Made and How They Work
A clearer understanding of how vaccines are made and what they do raises even more questions about the risk/benefit ratio.
Vaccines work by stimulating and exciting an immune response. The efficacy of a vaccine is measured by the production of antibodies. This stimulation of antibody production is achieved (or not) when either a live or killed virus or other vaccine agent is injected into a child or adult. The theory is that this antibody response will then be replicated to protect the vaccinated individual from future exposures.
For live virus vaccines, a virus is grown on mediums that include aborted fetal tissue and tissues from monkeys, cows, chickens, dogs, mice, and other animals. Growing the live viruses on animal cells is supposed to make them less virulent to humans yet still strong enough to induce an immune response. This virus is then manufactured with a variety of additives and preservatives to make the serum injected as a vaccine.
Non-live virus vaccines include bacterial toxins, “killed” whole virus, and proteins (among other things) and require the use of “adjuvants” to stimulate an immune response. These adjuvant-stimulated responses create the antibodies that are the measures of success of the vaccine. However the antibodies are not necessarily effective measures of true immunity from either live or non-live vaccines.
Additionally, the concept of Original Antigenic Sin calls into question whether the immune response from a vaccine (live virus or otherwise) could ever provide adequate protection.
The most commonly used vaccine adjuvant is aluminum, a heavy metal that is a known neurotoxinassociated with brain dysfunctions, including dementia and Alzheimer’s disease. Aluminum can last up to eight years in the brain resulting in cumulative neurological damage from additional exposures.
Vaccines and Autism
Despite all the reporting to the contrary, vaccines have been definitively linked to autism. In 1986, a class-action lawsuit against vaccine manufacturers by hundreds of parents whose children experienced regressive autism following vaccination resulted in legislation that absolved vaccine makers from liability and created a program which pays compensation for injury. As the class-action case wound its way through that system, most of those parents’ claims were rejected until Hannah Poling. Her case was championed by her father, Jon Poling, MD, PhD, a neurologist and professor at the Medical College of Georgia.
According to the 2011 article “Unanswered Questions from the Vaccine Injury Compensation Program: A Review of Compensated Cases of Vaccine-Induced Brain Injury” in the Pace Environmental Law Review, in order to file a claim of injury in the Vaccine Injury Compensation Program, parents of injured children are pressured to blame any autism spectrum brain injuries on non-autism causes. Typical symptoms of autism such as brain swelling (encephalitis) and seizures have been compensated for as long as parents define them as side effects of the vaccine rather than calling them symptoms of regressive autism caused by the vaccine.[vii] Today 1 in 68 children has Autism according to the CDC.
Numerous studies listed at the US National Library of Medicine National Institute of Health, link vaccines to autism. Several online articles suggest a correlation between the uses of aborted human fetal cells with the coincidental rise of autism.
One such study is Timing of Increased Autistic Disorder Cumulative Incidence by Michael E. McDonald and John F. Paul, NHEERL/EPA, published in February 2010 in Vol. 44 of the Environmental Science & Technologyjournal. It reports that a spike in autism seen in 1995 corresponds with the introduction of human DNA to the MMR vaccine, suggesting a possible link.
One very troubling danger that results from the way vaccines are produced is cross-species viral contamination. For example, the SV 40 virus, a simian virus, was transferred from monkeys to humans by growing the polio virus on monkey kidneys; the SV 40 virus causes human cancers (Journal of the National Cancer Institute, 1997). The virus was injected into hundreds of millions of healthy people worldwide who received early versions of polio vaccines from 1955 -1963.
According to an article published and available from The National Center for Biotechnology Information in a 2007 review of numerous studies about SV40 in humans, researches said the following: “SV40 footprints in humans have been found associated at high prevalence with specific tumor types such as brain and bone tumors, mesotheliomas and lymphomas and with kidney diseases…” Once infected, people with SV40 can pass the virus on to their children.
Knowing Vaccine Risk and Contraindications
Vaccines are defined as unavoidably unsafe by the CDC, the FDA, HHS, and legal precedent. Yet there is only minimal benefit to individuals and the community for protection from diseases that are unlikely to cause either severe illness or death outside of Third World countries.
The risks for each vaccine are stated right on the vaccine package inserts but these inserts are not given to parents or even to adults considering the suggested vaccines for them. It is also doubtful that the doctor or nurse dispensing the vaccine has fully read the product insert. For example, do doctors know that the Sanofi Pasteur Tripeda PI lists autism as one of the serious post marketing reactions to their MMR vaccine?[v] If parents knew that, they might reconsider giving the child the vaccine.
When patients ask for product information, they’re given an abridged version, one that would be unlikely to contain the full list of adverse events. That patients do not get the inserts can be especially problematic when pharmacists dispense flu vaccines; pharmacists do not have the same relationship with the patient and will not necessarily be aware of contraindications for a particular person.
A full list of contraindications and adverse events listed in the package inserts is available on the Immunization Action Coalition website. While the incidence of any particular adverse reaction listed on the insert may not be unacceptable in the eyes of the manufacturer or the CDC, every parent has both the duty and right to know what they are so that they can decide whether the benefit outweighs the risk for their child or themselves.
Scientific literature also shows that the vaccines can cause the diseases they’re meant to prevent, such as in the case of measles, whooping cough, and chicken pox (and others) when the vaccinated child sheds virus to family and community members, even if the child shows no symptoms. More troubling is that outbreaks are now occurring more often in late teen/young adult populations a time when childhood disease are more problematic. This shows that whatever immunity was originally conferred wears off over time. The only solution is even more boosters.
Yet if these individuals had gotten the infections in childhood, they’d have life-long immunity. Plus that immunity would be able to be passed from mother to child in breast milk, thus protecting the infant in the first years of life when they are most at risk for complications. This benefit does not exist in vaccine-induced immunity and therefore puts infants at greater risk for acquiring the infections in infancy rather than childhood.
Non-existent Benefit: Vaccine Antibodies Don’t Guarantee Immunity
Vaccine makers do not guarantee that their product does anything more than increase antibody levels in most people. They further admit that such antibodies do not necessarily mean immunity from illness.
For example, the Galaxo-Smith-Kline flu vaccine insert states: “Specific levels of hemagglutination inhibition (HI) antibody titer post vaccination with inactivated influenza virus vaccines have not been correlated with protection from influenza illness but the HI antibody titers have been used as a measure of vaccine activity. In some human challenge studies, HI antibody titers of ≥1:40 have been associated with protection from influenza illness in up to 50% of subjects.”
In simple language this means that the manufacturer does not claim that the flu vaccine protects from the flu; they only claim that it increases antibody activity in some people. However the increased antibody activity has only been associated with protection from the flu for half of the subjects whose antibodies reach the appropriate mark. For the other half, it is useless.
Some reports from analysis of the effectiveness of flu vaccines shows that they have up to an 84% failure rate. One reason for such a high failure rate is that the antibody against one influenza virus type or subtype confers little or no protection against another virus. Furthermore, the antibody for one antigenic variant of influenza virus might not protect against another antigenic variant of the same type or subtype. Frequent development of antigenic variants through antigenic drift is the virological basis for seasonal epidemics and the reason for the usual replacement of one or more influenza viruses in each year’s influenza vaccine.
Merck’s chicken pox vaccine has similar wording about effectiveness on its insert: “VARIVAX induces both cell-mediated and humoral immune responses to varicella-zoster virus. The relative contributions of humoral immunity and cell-mediated immunity to protection from varicella are unknown.”
This claims that the vaccine induces both the innate and humoral immune system responses yet they don’t know if the contribution is effective protection.
So, the benefits for vaccination in a healthy, well-nourished child or adult, it seems then, are not substantial. However, the risks associated with vaccines are substantial.
Science Fraud and the Media
Getting credible independent scientific evidence for vaccines is not always easy. As was the case with the tobacco industry, pharmaceutical companies pay either directly or indirectly for much of the science that is published. The revolving door of officials in government moving into highly paid positions in the pharmaceutical industry or lobbying also is problematic. The government seems to have a vested interest in not publishing information that would show vaccines in a poor light.
For example, in a statement released in August 2014 on his lawyer’s website, CDC scientist William Thompson, PhD, admits to falsifying data that showed a statistical connection between the MMR vaccine and autism spectrum disorders in African American boys who are given the vaccine before the age of three. Dr. Thompson published a paper in the journal Pediatrics claiming there was no connection. Ten years later, he admitted his fraud after conversations he had with another scientist were recorded without his knowledge. Part of that release reads:
My name is William Thompson. I am a Senior Scientist with the Centers for Disease Control and Prevention, where I have worked since 1998. I regret that my coauthors and I omitted statistically significant information in our 2004 article published in the journal Pediatrics. The omitted data suggested that African American males who received the MMR vaccine before age 36 months were at increased risk for autism. Decisions were made regarding which findings to report after the data were collected, and I believe that the final study protocol was not followed.
While Thompson still believes that the risk from disease is greater than the risk from vaccines, it is doubtful that many families whose children have autism would agree with him. He has not lost his job or been prosecuted for his admitted fraud.
In another case, a scientific journal rather than a doctor perpetrated the fraud. The case of Andrew Wakefield, MD, made news when he was accused of fraud for a paper he’d authored with multiple colleagues. The paper had appeared in the British journal Lancet in 1998 and it linked a gastrointestinal problem with autism; the authors suspected the gastrointestinal problem was caused by vaccination. Allegations of fraud, improper ethics, and conflict of interests were made by a reporter in 2004 who worked for Rupert Murdock’s Sunday Times. The reporter’s allegations were disputed not only by the authors but also by the editors of Lancet and the institution where the research was conducted, University College London. However the accusations gained traction when members of Parliament became interested and held hearings.
Media that included the scientific journal, the British Medical Journal (BMJ), and traditional media launched a vicious attack blitz against Wakefield and his colleagues. The original research paper was eventually withdrawn by Lancet and the authors charged with fraud by the Royal College of Medicine and the courts. Ten of the 13 co-authors caved to the pressure but the three authors who refused to retract their findings were found guilty and stripped of their medical licenses. The headlines went worldwide condemning the men and the connection they’d tangentially made to vaccines and autism.
However, the original paper and its authors were eventually exonerated after more than a decade of struggle against their attackers. Those facts did not make any headlines in any media. The doctors were returned to the medical register, though no apology was forthcoming.
The reporter who originally leveled the false charges won prestigious news awards, which were not withdrawn even when it was shown in court proceedings that he had reported falsely, hid relevant exculpatory documents, and had many conflicts of interest. The reporters ally, the editor of the BMJ, admitted that the BMJ receives advertising and sponsorship revenue from GSK and Merck (MMR manufacturers).
The BMJ editor, in testimony before Parliament, admitted, “Even on the peer review side of things, it has been said that the journals are a marketing arm of the pharmaceutical industry. That is not untrue.”[vi]
What other information is spread falsely? One piece gaining traction is that women, children and the elderly should have routine flu vaccines.
Influenza Vaccines, Pregnant Women, Children & the Elderly
Pregnant women and the elderly are now encouraged, even shamed or browbeaten, into getting flu vaccines. Here is a sample of the wording on influenza vaccine inserts (it’s almost exactly the same for all the influenza vaccines listed on IAC’s website):
Safety and effectiveness of AGRIFLU has not been established in pregnant women, nursing mothers, and children. Antibody responses were lower in the geriatric population than in younger subjects.
Safety and effectiveness of AFLURIA have not been established in pregnant women or nursing mothers. Antibody responses were lower in geriatric subjects than in younger subjects. AFLURIA is not approved for use in children less than 5 years of age because of increased rates of fever and febrile seizures. One comparator controlled trial demonstrated higher rates of fever in recipients of AFLURIA as compared to a trivalent inactivated influenza vaccine control.
Safety and effectiveness of FLUARIX have not been established in pregnant women or nursing mothers. Register women who receive FLUARIX while pregnant in the pregnancy registry by calling 1-888-452-9622. In a clinical study of children younger than 3 years of age, antibody titers were lower after FLUARIX than after an active comparator. Geriatric Use: Antibody responses were lower in geriatric subjects who received FLUARIX than in younger subjects.
Reproduction studies have been performed in rats at a dose approximately 300 times the human dose (on a mg/kg basis) and have revealed no evidence of impaired fertility or harm to the fetus due to Flublok. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this vaccine should be used during pregnancy only if clearly needed.
Safety and effectiveness of Fluzone has not been established in pregnant women. Antibody responses to Fluzone are lower in persons >65 years of age than in younger adults.
Safety and effectiveness of FluMist Quadrivalent have not been established in pregnant women, nursing mothers, geriatric adults, or children less than 2 years of age. In clinical trials, in children 6 through 23months of age, FluMist was associated with an increased risk of hospitalization and wheezing.
If the package inserts say the flu vaccine has not been established as safe for pregnant women, is not very effective in the elderly, and causes problems in small children, why is it being pushed now at such an extreme level?
Vaccines, Foreign DNA, and Chronic Disease
In addition to the list of known adverse effects, and that vaccines have been definitely linked to the spread of the cancer causing SV-40 virus (simian virus 40) in humans, what other problems are we creating?
Scientists are also correlating the huge rise of chronic autoimmune diseases with the increased rise in numbers of vaccines given. While other environmental factors also contribute to the rise of chronic disease, vaccines cannot be eliminated as a contributing or causal factor.
When foreign DNA is injected into humans, the body’s immune response is to attack that foreign DNA. When that foreign animal DNA attaches to the human cells, the immune response includes attacking its own cells. Animal DNA or foreign fetal cell DNA in vaccines can also be taken up by an individual and recombined into their DNA. Also, according to Helen Ratajczak, a former senior scientist at a pharmaceutical firm, there is a link to brain damage and human DNA in vaccines.
Aside from the DNA issue, that some vaccines are grown on aborted fetal tissue is an issue for people with a moral or religious objection for abortion. (Vaccines that contain aborted fetal tissue can be found online here http://www.soundchoice.org/certification.html.)
There is a limit to how much foreign material our bodies can handle before genetic damage occurs. Each person has his or her own unique genetic blueprint which responds to foreign substances differently. It appears that many children are hitting that limit.
This generation of children in the United States is sicker than any previous generation with over 50% of children experiencing one or more chronic illness. Many of those illnesses are autoimmune diseases. The US ranks 19th among developed nations in infant mortality. It also has the most highly vaccinated children beginning on the day a child is born.
Could these terrible statistics be linked to the cumulative adverse effects of too many doses of vaccines?
What’s a Parent to Do?
Learn more. Be your child’s best advocate (and your own).
The Vaccine Research Library has a collection of more than 6,500 articles gleaned from peer-reviewed journals. The articles document conflicts of interest in medical research, and chronicle and present undeniable evidence of vaccine injury that includes allergies, autoimmune disease, and a long list of neurological disturbances.
The US National Library of Medicine has more than 300 research studies regarding vaccine dangers: http://www.greenmedinfo.com/guide/health-guide-vaccine-research.
The CDC collects doctor’s reports of thousands of serious vaccine reactions each year including hundreds of deaths and permanent disabilities. http://www.cdc.gov/mmwr/preview/mmwrhtml/ss5201a1.htm#tab3http://www.cdc.gov/mmwr/preview/mmwrhtml/ss5201a1.htmhttp://www.cdc.gov/MMWR/PDF/ss/ss5201.pdf
Follow the money
As you do your research, be mindful of who benefits from the information you’re reading. Ask: Who paid for the study? Who made the campaign contributions? Who paid for the advertising? Pharmaceutical companies have deep pockets and they spread their money around in ways that suit them best. The big question is, does what suits the pharmaceutical industry benefit our children?
Contact your members of Congress
Before any mandates become law that we must vaccinate our kids, demand independent investigations into the manufactures of vaccines, their adjuvants, excipients, and growing mediums. We deserve that kind of transparency and not bureaucratic, corporate, and media spin.
[ii] Wade Baker and Rita Baker, Plaintiffs-Appelants, v. United States of America Defendant-Appellee. No. 86-5578. Dec. 4, 1986; as quoted on vactruth.com/2013/02/10/vaccines-are-unsafe/
[iii] Vaccine Epidemic; p 138
[iv] Autism, The Misdiagnosis of Our Future Generations (abridged version), testimony to Congressional Subcommittee Hearing on May 6, 2004. Copyright Advanced Concepts in Medicine, Rashid A. Buttar, DO, FAAPM, FACAM, FAAIM
[vi] Dissolving Illusions; pg 337
[viii] From a press release on May 1, 2015 at the close of Autism Awareness Month; www.benzinga.com/pressreleases/12/05/p5465972/autism-awareness-month-closes-statistics-reveal-alarming-futre-suggest
links | Wie ben ik? Who am I? | OOR4U Guilde | Information on vaccinations on this website: | Information on cancer on this website | Naturally, Happily, Healthily, Toxin Free Diet and Care (e4dc) | Voorwoord en Inleiding Geraffineerdesuikergevoeligheid, en contactgegevens Scentses | | Wat is geraffineerdesuikergevoeligheid en Waarom worden bij geraffineerdesuikergevoeligheid sommige suikers wel en andere niet verdragen? | Wat is suiker? Bouw van suikers/koolhydraten | Snelle en langzame suikers | Bloedsuikerspiegel en hormonen | Wat is het verschil tussen tot nu toe omschreven hypoglykemie en geraffineerdesuikergevoeligheid? | Het verschil tussen hypo's en hypers bij suikerziekte , bij hypoglykemie en die bij geraffineerdesuikergevoeligheid. Waarom blijft de adrenaline reactie aanhouden?Hoe is het mogelijk dat er zo snel na geraffineerdesuiker inname al een reactie plaat | Verschillende soorten hypoglykemie en andere hormoongebonden complicaties bij geraffineerde koolhydraten vertering/opname en bloedsuiker instandhouding Overeenkomsten en Verschillen tussen Geraffineerdesuikergevoeligheid en ADHD | Kunstmatige suikers | Geraffineerdesuikergevoeligheid in de praktijk | Gewoon Genietend Gifvrij Gezond dieet en verzorging (G4dv) | Waarom is de informatievoorziening over E-nummers en plotselinge extreme humeurigheid na inname van geraffineerde suiker zo gebrekkig?Misinformatie en schijnonderzoeken over plotselinge extreme humeurigheid na inname van geraffineerde suikerInformatieve | Informatievervuiling: Onwetendheid, Slordigheid, of Opzettelijke Misleiding? | Conclusie | Bronverwijzingen | Bijlagen 1 t/m 7monosachariden, 2. Disachariden, 3 polyol, 4 producten met aspartaam, 5 Giftige E nummers in degelijk lijkende produkten, 6 Safety card Natronloog of te wel E524, toevoeging van sommige cacao merken!, 7 Soja, | Appendix 7a Sucralose | Bijlage 8 Vitaminen, Mineralen, Sporenelementen, Eiwitten, Vetten, Koolhydraten in Voedingsmiddelen, Kruiden | Bijlage 9 Himalayazout | Bijlage 10 Toxic Ingredients You Should Avoid | Bijlage 11 Bijwerkingen Ritalin(Methylfenidraat) | Bijlage 12 Aspartaam, hoe een stof wat gaten in de hersens van muizen brandt veilig voor menselijke consumptie werd bevonden. | Bijlage 13 Hypoglycemia | Bijlage 14 Budwig | Bijlage 14a Geitenmelk: waarom het lichter verteerbaar is dan koemelk | Bijlage 15 E nummers | Bijlage 16 Cadeaus om te vermijden | Bijlage 17: Dieetmaatregelen tegen kanker | Bijlage 18 "Hoe tanden in elkaar zitten." | Bijlage 19 kankercellen uitroeien door suikers te vervangen door gezonde vetten | bijlage 20 meer over kankergenezing | bijlage 21 Zuurzak Soursop | Bijlage 22 Crisis en oplossingen: roggker=recht op gezondheid, geluk, kennis en rechtvaardigheid | Bijlage 23 Milieuschandalen (hier stond eerst de G4dv, die is verplaatst naar de beginpagina) | Bijlage 24 Het Echte Nieuws over gif in het milieu | Bijlage 24 a Hout | Bijlage 25 vooronderzoek G4dieet | Bijlage 26 Vooronderzoek TVtandpasta | Bijlage 27 Voorbeelden van de denkfout in de Westerse Medische Wetenschap, waardoor ze steeds de plank misslaan als het aankomt op bepalen wat gezonde voeding is: Calcium en beta caroteen | Bijlage 28 Kruiden | Bijlage 29 Vitamines, Mineralen, eiwitten, vetten em koolhydraten | Bijlage 30 Gevaar van magnetron en vooral van in voedsel in plasticbakken verwarmen | bijlage 31 Schema voedingsmiddelen:vitamines, mineralen, eiwitten, vetten en koolhydraten | Bijlage 32 Schema Bedenkelijke stoffen, E-nummers, toevoegingen, giffen | Gifvrij dieet en Gifvrije verzorging | Bijlage 33 kankerbestrijding | bijlage 34 Het gevaar van pinda's | Bijlage 35 Proteïnen in yoghurt | Bijlage 36 Eten uit de natuur | Bijlage 37 Superfoods: a.Aloë Vera, b.Omega 3-6-9 olie, c.Kefir, d.Kombucha, e.Yoghurt, f.Cranberrysap,g. Gember, h.walnoten, i. zonnebloempitten, j. bosbessen, k.zeewier, l.wortelsap, m.ginkgobiloba,n. guldenroede, o.peu dárco, p. driekleurig | Bijlage 37 a. Aloe Vera | Bijlage 37.b. Omega 3 saus | Bijlage 38 The Problem with Wheat | Bijlage 39 Himalaya Zout vs De rotzooi die voor zout doorgaat | Bijlage 40 Benefits of Goats milk over Cows milk | Bijlage 41 The problem with most vegetable oils and margarine | bijlage 42 for healthy bones calcium, vitamin D, vitamine k2, magnesium, trace elements | Bijlage 43 The dangers of acrylamide (carbohydrates baked above 210 degrees Celcius) | Bijlage 44 Gevaren van plastic, aluminium en andere verpakkingsmaterialen | bijlage 45 Dangers of Fishoil and better sources for omega 3 | bijlage 46 fruit tegen kanker (aardbeien, cranberries etc) | bijlage 47 Hoog tijd voor een nieuwe schijf van 5 | bijlage 48 Uitleg hoe inentingen autisme veroorzaken door glutamaat productie in de hersenen te stimuleren wat schadelijk is voor de hersenen en voor de hersen ontwikkeling | bijlage 49 Korte Geschiedenis van Monsanto, pagina van Dr Mercola± In Amerika vechten ze voor wat hier heel gewoon is±etiketten waar op staat wat er in voedsel zit. | Bijlage 50 Nep ADHD diagnoses | Bijlage 51 Vrouw vertelt over uitgelekt NASA document over oorlog tegen de mensheid | bijlage 52 Bij medicijn dat zogenaamd cholesterol verlaagd juist 52$ hogere kans op plak in de aderen rondom het hart/ 52@ higher chance of heart plaque when tajking certain cholesterol lowering medicines. | Bijlage 53 Welke oliën zijn veilig om te verhitten? | Bijlage 54 Dr Mercola over Genetisch Gemanipuleerd voedsel | bijlage 55 Dr Mercola: genetisch gemanipuleerd voedsel: ontworpen om insecten te doden, maar het maakt ook onze cellen kapot. | Bijlage 56 Dr Mercola Alzeheimer detectie methode, en g4dv ook preventief voor Alzheimer | Bijlage 57 Het einde van het antibiotisch tijdperk aangebroken door toenemend aantal antibiotica resistente bacteriën, Ook hierop is de g4dv een antwoord. | Bijlage 58 Vaccinaties gaan om geld, niet om ziektebestrijding | Bijlage 59 Artikel Dr. Mercola over kankerverwekkende zaken in persoonlijke verzorgings- en huishoud producten | Bijlage 60 Dr. Mercola: Pesticiden kunnen neurologische schade aanrichten, gebruik liever etherische olie voor huisdieren en plant liever goudsbloem in de tuin | Bijlage 61 5 miljoen chronisch zieken in Nederland, zorg VS ook waardeloos | Bijlage 62 Gevaar vaccinaties | Bijlage 63: Gevaren antibiotica in vlees (artikel va Dr. Mercola) | Bijlage 64: Gevaren Testosteron behandeling | Bijlage 65 transvetten zijn de boosdoeners, verzadigde vetten zijn juist goed! (Dr Mercola) | Bijlage 66: Hippocrates Health Institute | Bijlage 68:NVWA hoge boetes voor gezondheidsclaims | Bijlage 69: Voor een gezond hart heb je gezonde vetten nodig | Bijlage 70 Eieren moet je bewaren op kamer temeratuur, niet in de koelkast! | Bijlage 71: Gevaren van niet gefilterd water | Bijlage 67:Boetes voor het zeggen dat iets buiten de farmaceutische industrie gunstig voor de gezondheid is | Bijlage 72 Vitamine D bronnen | Bijlage 73 Chiazaad voedingsinformatie | Bijlage 74: Voordelen van gefermenteerd voedsel | Bijlage 75 9 voedingsmiddelen die je nooit moet eten | Bijlage 76 Top 10 artikelen van Dr. Mercola van 2013 | Bijlage 77: Dr Mercola: De beste wapens tegen griep. | bijlage 78 The secret of longevity | bijlage 79 Het Grote Vaccinatie Debat 15 december 2013 | Appendix 80 Lead Developer Of HPV Vaccines Comes Clean, Warns Parents & Young Girls It?s All A Giant Deadly Scam | Biijlage 81 How Grazing Cows Can Save the Planet, and Other Surprising Ways of Healing the Earth | Bijlage 82 De Verborgen Gevaren van Vaccinaties | Bijlage 83 CDC Admits as Many as 30 Million Americans Could be at Risk for Cancer Due to Polio Vaccine | Bijlage 84 We hebben 100 keer meer microben dan cellen in ons lichaam. De meeste helpen ons. Zullen we hun ook helpen? | Bijlage 85 Belang van licht en slaap | Bijlage 86 Artikel Dr Mercola over vergissingen in voeding die tot voedings tekorten leiden. | Bijlage 87 In Amerika beïnvloedt Junkfoodindustrie diëtistenopleidingen | bijlage 88 Dr Coldwell: Elke kanker kan in 2 tot 16 weken genezen worden | Bijlage 89: Want to Know over Tetanus | Appendix 90: Dr. Russel Blaylock | Bijlage 91 Wat zijn opvliegers? | Bijlage 92, Dr Mercola: One in 25 Patients End Up with Hospital-Acquired Infections, CDC Warns | Bijlage 93 Dr Mercola Toxic Combo of Roundup and Fertilizers Blamed for Tens of Thousands of Deaths | Bijlqge 94 New Studies Show Optimizing Vitamin D Levels May Double Chances of Surviving Breast Cancer, Lower LDL Cholesterol, and Helps Prevent Autism | Bijlage 95, Dr.Mercola: How Vitamin D Performance Testing Can Help Optimize Your Health | Bijlage 96: Be Wary About This Food - It Can Wreck Your Ability to Walk, Talk, and Think | Bijlage 97 Gevaren van Vaccinaties (Mercola) | Bijlage 98: Ouders moeten geïnformeerd worden over de gevaren van vaccineren om een goede keus te kunnen maken | Bijlag 99: Zonnebrandmiddelen gevaarlijker dan zon als het gaat om huidkanker | Bijlage 100 Ignoring This Inflammatory Early Warning Signal Could Cost Your Life | Bijlage 101 Mijd Giffen, Niet Voedingsmiddelen! | Bijlage 102 Mentale rust | Bijlage 103: Voordelen van Kurkuma | Bijlage 104: Dr Mercola article Kruid tegen kanker | No Words | Bijlage 105: Dr Mercola: Sun , vitamin D and vitamin B3 crucial for longevity | Bijlage 106 Cowspiracy film en kritiek | Bijlage 107 Artemesia een effectief anti-malaria kruid | Bijlage 108, Chemotherapie is gevaarlijk | Bijlage 109 Canola oil, what is it, and is it good or bad for people? | Bijlage 110 Are peanuts good or bad for you? | Bijlage 111 Halloween recipes | Bijlage 112 Vaccinatieschade | Bijlage 113 Immigrants seek herbal remedies | Bijlage 114 more_doctors_confessing_to_intentionally_diagnosing_healthy_people_with_cancer | Bijlage 115 Dangers of vaccinating pregnant women | Bijlage 116 Omega 3-6-9 mengsel | Bijlage 117 Waarom er geen koolzaadolie zit in het omega 3-6-9- mengsel van de g4dv | Bijlage 118 Vaccinaties | Bijlage 119 Judy Wilyman, PhD on amti vaccination | Bijlage 120 Wetenschappelijke argumenten die de Keshe scam blootleggen | Bijlage 121 ECEH bacterie | Bijlage 122 grains | Bijlage 123 Make your own chocolate | Bijlage 124 Vaccine Violence | Bijlage 125 Italian court rules mercury and aluminum in vaccines cause autism: US media continues total blackout of medical truth | Bijlage 126 Dr Mercola: Vaccines and Neurological Damage | Bijlage 127 Why many doctors do not vaccinate their own children | Appendix 128 2 centuries of officoial statistics show vaccines did not save us and These graphs show why many doctors don't vaccinate their own children and Vaccines: A Peek Underneath the Hood | Bijlage 129 Leaflet Infanrix | Bijlage 130 Vaccine Madness | Bijlage 131 Japanse slachtoffers vaccin baarmoederhalskanker slepen overheid en farmareuzen voor de rechter | Bijlage 132 Pregnancy, labour, delivery and child care | Appendix 133 healing diet for our canine friends | Bijlage 134 Flowchart edible or non-edible | Bijlage 135 Keeping children healthy naturally | Bijlage 136 Vaccines and the Amygdala | Bijlage 137 Revolving door between politics and big pharma explained | Bijlage 138 Ingredients Vaccines | Bijlage 139: Medisch scheikundige geeft drie redenen waarom hij zijn kinderen niet laat vaccineren | Bijlage 140 Ryan's story | Bijlage 141 NVKP lezingen dr Hans Moolenburgh | Bijlage 142 HPV vaccine | Bijlage 143 Dr. Hans Moolenburgh over fluoride | Bijlage 144 Baby dies three days after getting six vaccines | Bijlage 145 Interview Trouw met Dr Hans Moolenburgh | Bijlage 146 Jacob van Lennep | Bijlage 147 Flow chart "to believe or not to believe medical or nutritional advice" | Appendix 148 The case experts make against vaccines | Apendix 149 Dr Mercola article: Experts admit Zika threat fraud | Appendix 150 Sudden deaths among health advocates | Appendix 151 Thimerosal | appendix 152 Herd immunity? | Appendix 153 Formaldehyde in vaccines | Appendix 154 Why doctor's say "Do not take the flu shot!" | Bijlage 155 Vaccineren? Natuurlijk niet! En wel hierom: | Appendix 156 Vaccine makers bypass WHO regulations | Bijlage 157 Het probleem van overbehandeling bij borstkanker | Bijlage 158 Chemotherapie vermoordt u | Bijlage 159 Borstbesparende operatie beter dan amputatie voor overlevingskansen bij borstkanker | Appendix 160 Vaccine induced bone fractures | Bijlage 161 hulpstoffen in Vaccins toegegeven door CDC | Appendix 162 meningitis: symptoms, how to prevent, how to treat | Appendix 163 Training of nutrtionists often shady | Appendix 164 Molecular Biochemist Dr.Lucija Tomljenovic, PhD, explains why vaccines not only don't work, but are extremely harmful and can be lethal as well | Appendix 165 CDC knew about MMR vaccine autism link as early as 1999, but covered it up | Appendix 166 Scientists at the vaccine safety debate January 2011 | Appendix 167 Vaccinated children 5 times more likely to contract auto immune diseases | Appendix 168 Before and after vaccine: this is what mass brain destruction looks like | Appendix 169 Hepatitis B vaccine | Appendix 170 Countries where vaccines are not mandatory and the nazi roots of vaccines and drugcompanies | Appendix 171 The dangers of soybean oil | Appendix 172 Vaccines do not protect against Measles | Appendix 173 HPV vaccine | Appendix 174 Hoogleraar Peter Gøtzsche en anderen over corruptie in de farmaceutische industrie | Appendix 175 Dr Arlan Cage | Appendix 176 How vaccines damage your immune system | Appendix 177 Vaccines are not tested properly | Appendix 178 Documentaries exposing pharma fraud | Appendix 179 Dr Suzanne Humphries | Appendix 180 Dr Russel Blaylock: Vaccinations can kill you or ruin your life | Appendix 181 Doctors who clearly explain why vaccines are neither safe nor effective | Appendix 182 Dr Sherri Tenpenny | Appendix 183 Alan Phillips attorney Vaccine Rights | Appendix 184 Dr Rebecca Carley | Appendix 185 Vaccines bargain basement of the medical industry, says Maurice Hilleman (who developed 36 vaccins) admits AIDS and Cancer causing virusses were added to vaccines | Appendix 186 Many independent studies show vaccine dangers, Damages paid by pharmaceutical companies for vaccine damahge | Appendix 187 The truth behind Vaccinations | Appendix 188: Guess what happened to Nazi war criminals responsible for the genoside of millions: After aquittal or a short prison sentence they went back to being CEO's for big Pharma! | Appendix 189: Mercola: What?s the Right Dose of Exercise for a Longer Life? | Appendix 190 What happened to Dr Mercola? | Bijlage 191: hoofd RIVM zegt Kindervaccinaties veroorzaken hersenvliesontsteking | Appendix 192: Use up stock even though proven unsafe or use cheaper less safe vaccines | Appendix 193: WHO report reveals: Vaccines are made in China without safety control | Appendix194: Vaccine Court has paid 3.7 billion in damages to families | Appendix 195: Autism in California skyrocketed since mandatory vaccination | Appendix 196: MMR Vaccine Causes Seizures in 5,700 U.S. Children Annually | Appendix 197: The history of vaccines | Appendix 198: Studies show unvaccinated children are much helthier than vaccinated ones | Appendix 199: The vaccine-shaken baby syndrom link | Appendix 200: vaccines cause SIDS | Appendix 201: The Dangers Of Vaccines and Vaccination | Appendix 202: Vaccines and the peanut allergy epidemic | Appendix 203: The neurotoxicity of vaccines | Appendix 204: Statistics | Appendix 205:Nervous System | Appendix 206: 6 reasons to say NO to vaccination | Appendix 207: Celebrity anti vaxxers | Appendix 208 Dr John Bergman | Appendix 209 Measles: natural prevention and remedies | Appendix 210: Hepatitis B prevention and treatment | Appendix 211: Dr Shiv Chopra. PhD Microbiologist, vaccine expert | Appendix 212: Thimerosal breaks down into ethyl mercury in the body, and is 50 times more toxic than the methyl mercury found in fish | Appendix 213 Dr Dale Brown | Appendix 214 Vaccines cause autism | Appendix 215 Statistics infant mortality per country | Appendix 216: How to lower glutamate levels in the brain | Appendix 217 David Getoff Laatste wijziging op: 19-02-2018 20:44