Vaccines, autism, and the compulsory vaccination debate.
The debate concerning vaccines as a trigger for autism has been ongoing for many years even though the evidence to confirm this fact has been in the public domain for just as long. Unfortunately the boards and controlling bodies are not being completely forthcoming when presenting the facts and the power of corporations to attack and ruin the lives of any scientist who presents facts that highlight vaccine shortcomings should also be taken into consideration, Andrew Wakefield being a prime example of this. We also have to consider the industry’s ability to change governmental policy through lobbying (bribery) and media manipulation(7). Corporations have no feelings or personal considerations and use manipulation of the media as a tool for attacking competitors, even if it is at the expense of the general public(8). We must understand that the welfare of the general public is not a consideration of corporations or governing health bodies. The infiltration of our health societies and controlling bodies by vaccine corporations has been documented from their inception(4).
This media manipulation by the vaccine industry can be seen in modern times when considering the presentation given by the United States Centers for Disease Control and Prevention (CDC) director of media relations and communications Glen Nowak. In his presentation Glen Nowak explains how to use scare tactics as a "recipe" for "fostering public interest and high vaccine demand". He explains how to use the media to give people the "perception" that many people are falling ill and the "perception of vulnerability". He talks about how to use the application recommendations for 50-64-year olds and babies between 6-23 months as tools to "imply" it is helping the infirm and that they have data of that precision(9). This is only done to boost the profit of the vaccine industry and the corruption of the CDC by biopharmaceutical companies has been documented by Jeanne Lenzer, the associate editor of the British Medical Journal (BMJ) in her article(10). This is confirmation that the general public will be misled by the controlling bodies in order to boost the profits of associated corporations making the advice given unfit for purpose.
The manipulation of health agencies can also be seen in the recent change in guidelines from the UK health department where on page 5 you will see that a clause has been worded in a way to allow children under the age of 16 to accept vaccinations while at school even if it is against their parent’s instructions. Clearing the way for mass vaccination of children to legally be undertaken at school with coercion from good intentioned teachers who are also misinformed. Compulsory vaccinations have been tried many times in the past and they have resulted in large numbers of deaths throughout history, the Spanish Flu epidemic being the most prominent example. It is recognised in the literature that it did not originate from Spain and although it is suggested that it started in British Army camps (1). The influence of the compulsory vaccination program of US military personnel that dates back over 200 years should not be overlooked(3). Compulsory vaccinations during the early 1900s caused many unnecessary deaths that were documented in a 1920 book called Horrors of Vaccination by Chas. M. Higgins. The book was written as a petition to the US president to abolish punishment for military personnel who refused the vaccine(4). The deaths were highlighted by Mr Higgins in great detail and precision, while the medical industries reluctance to record the cause of these deaths honestly were also noted and proven(4). This duplicity is still going on today when we consider the renaming of polio that is contracted through vaccination as “non-polio acute flaccid paralysis (NPAFP). Why not call it vaccine induced polio? The connection between the oral polio vaccination (OPV) and NPAFP was established by the Department of Paediatrics, St Stephens Hospital, Delhi study that documented 47,000 children had acquired the disease and were newly paralysed(5), this was also confirmed in a later study(6).
Vaccines are not completely safe and in many cases cause great harm to innocent, healthy children as well as adults. The damage to children is most publicly discussed and disputed by the industry when considering autism. The mitochondria are the powerhouse of individual cells and a study by experts in neurology provided evidence that “autistic spectrum disorders can be associated with mitochondrial dysfunction”(11). It is further documented by experts in neurogenetics that the onset of autism in children with genetically dysfunctional mitochondria is closely related to the child experiencing a fever(12). Further assault on normal mitochondrial function comes from heavy metals. From experiments on rats, the neurotoxic effects of heavy metals is understood to compromise mitochondrial function(13), this was confirmed in a study using human T-cells(14), and also in a study of autistic children(15). The CDC claims there is no evidence that thimerosal causes any harm but many studies show that it damages mitochondrial function(16,17, 18, 19,) even at the minute levels in vaccines it is “significantly more toxic than the other metal compounds examined”(18). A study was conducted into the Hepatitis B vaccine and it found a 3 fold increase in the likelihood of a child to develop autism if they had the vaccine in the first month of life. It also found an elevated risk for receipt of early intervention or special education services. It found T helper 1 and 2 cytokine ratio imbalances and circulating anti-brain autoantibodies in 30 to 70% of subjects, with significantly increased pro-inflammatory cytokines that affected non-white children more severely(25).
After considering this information, it can be seen that injecting children who have a genetic predisposition to mitochondrial dysfunction with heavy metals, chemical toxins and live viruses that stimulate the inflammatory response of fever, will lead to a high probability for that child to develop autism. The link between autism and vaccinations was highlighted by Andrew W. Zimmerman MD when he submitted an affidavit to the court explaining how his advice for one particular case had been misused to make the erroneous claim that there was no connection between vaccines and autism. This claim is not representative of his views and this can be seen in the 2006 case study he co-authored that shows mitochondrial dysfunction after vaccines can be responsible for autistic regression(21).
Dr. Theresa Deisher obtained a Doctorate in Molecular and Cellular Physiology from Stanford University in 1990 and in 2014 conducted a study that found a direct link between the inclusion of foetal and retroviral contaminates in childhood vaccines and infants who later developed autistic disorder. Further it was found that Varicella and Hepatitis A immunization coverage was significantly correlated to autistic disorder cases. It was found that the change in autism rates coincided with the introduction of vaccines manufactured using human foetal cell lines rendering the vaccine contaminated with foetal and retroviral components(60).
In 2019 Diesher wrote an open letter to legislators in which she further highlights the fact that autistic children who undergo stem cell treatment using their own cord blood show significant behavioural improvements, suggesting that they are not suffering from autism of genetic origin, but autism that was acquired after birth(22).
A 2011 study found that the rate of autism rose dramatically after the introduction of the MMRII vaccine even though it did not contain thimerosal. However the rise in autism incidence coincided with the introduction of the MMRII vaccine in 1983 and a further rise was seen after 1988 when a second MMRII vaccination was recommended in the vaccination schedule. Furthermore, in 1988, MMR II was used in the United Kingdom, which reported a dramatic increase in prevalence of autism to 1/64. Canada, Denmark, and Japan also reported dramatic increases in prevalence of autism. It is important to note that unlike the former MMR, the rubella component of MMR II was propagated in a human cell line derived from embryonic lung tissue. The MMR II vaccine is contaminated with human DNA from the cell line. This human DNA could be the cause of the spikes in incidence. An additional increased spike in incidence of autism occurred in 1995 when the chicken pox vaccine was grown in human fetal tissue(76).
A 2016 study found that autistic children had higher levels of lead and mercury in their blood and had an altered excretory rate of porphyrin-containing rings that are responsible for the transport of iron around the body(73).
A 2017 study confirmed the role of toxic heavy metals in the aetiology of autism and also found that the problem was more pronounced in developing countries when compared to developed countries(72).
Aluminium (Al) adjuvants have never been proven safe, Professor C. Exley is a Professor in Bioinorganic Chemistry who explains Al is locked by chemical bonding with other elements into the earth and therefore normally excluded from the biological processes of living things until modern times. We are living through what Prof Exley refers to as the “aluminium age”. He identifies our use of Al in our everyday lives as the catalyst that releases Al from its bond, allowing it to enter biological processes of living things(28). He also concluded that Al is a catalyst of superoxide-driven biological oxidation that can lead to disease(26). He shows in another study that Al from vaccines represents an acute exposure and highlights the lack of understanding of Al toxicity by the medical profession. He explains that the major component of any vaccine is the Al adjuvant and when infants receive 1 vaccine they are exposed to the same amount of Al that they receive from either 150 days breast feeding or 25 days of the worst contaminated infant milk formula. He explains that the next vaccines are given before the 150 day period is up and so each vaccine adds to the body burden(27). He also found while studying the Camelford water disaster that a body mechanism exists which transported the Al when ingested and stored it in the brain tissue of a man who later developed epilepsy and died as a result of an epileptic fit(29).
A 2009 study into Gulf War Syndrome (GWS) showed that mice given an aluminium dose equivalent to two injections showed significantly increased apoptosis of motor neurons and increases in reactive astrocytes and microglial proliferation within the spinal cord and cortex. Aluminium was also found in the cytoplasm of motor neurons with some neurons also testing positive for the presence of hyper-phosphorylated tau protein, a pathological hallmark of various neurological diseases, including Alzheimer’s disease and frontotemporal dementia. It was therefore concluded that possible causes of GWS include several of the adjuvants in the anthrax vaccine and others. The most likely culprit appears to be aluminium hydroxide(62).
A 2012 study considered Al adjuvants and advised that infants should not be thought of as small adults, it recommended that they should have specially designed medical interventions that are not based on scaled down versions of the adult regime. Adult humans long-term exposure to aluminium vaccine adjuvants can lead to cognitive dysfunction and autoimmunity but in spite of these observations children continue to be exposed to much higher levels of aluminium adjuvants than adults, via routine childhood vaccination programmes. Vaccines have a predilection to affect the nervous system and were found to cause illnesses of an autoimmune nature. There are critical periods in brain development during which even subtle immune challenges (including those induced by vaccinations) can lead to permanent detrimental alterations of brain and immune function and a single aluminium adjuvanted hepatitis B vaccine administered to new-born primates within 24 hours of birth is sufficient to cause neurodevelopmental delays in acquisition of neonatal reflexes essential for survival. It was found that high exposures to aluminium adjuvants repeated over relatively short intervals during critical neurodevelopmental periods constitute a significant neuroimmunotoxicological challenge to neonates and young children. The study also advised that research evidence shows that increasing concerns about current vaccination practices may indeed be warranted because children may be most at risk of vaccine-induced complications and recommended a rigorous evaluation of the vaccine-related adverse health impacts in the paediatric population(30).
A 2013 study found that both the extremely toxic methylmercury (meHg) and ethylmercury (etHg) that is derived from the metabolism of thimerosal have similar outcomes for cardiovascular, neural and immune cells. It goes on to explain that etHg's toxicity profile is different from that of meHg, leading to different exposure and toxicity risks. Therefore, in real-life scenarios, a simultaneous exposure to both etHg and meHg might result in developing enhanced neurotoxic effects(59).
Mineral Oil Adjuvants have been found to catalyse an heightened immune response from vaccines from as far back as 1956(81) and peanut was first suggested from 1964(79). Groundnut and coconut was studied in 1996(80) and the inclusion of animal and food proteins in vaccines has been continued since. The injection of food proteins into the bloodstream causes and immune response and sensitisation that is further amplified with every subsequent exposure. It is therefore not too much of a stretch of the imagination to conclude that vaccines are responsible for the increase in allergic reactions within the general population.
Vaccine failures and manufacturing concerns are often reported. In 1979 a study looked at the way antibodies are made in response to measles vaccination. It found that children under one year old did not make antibodies in the same way and the vaccination failed even after two attempts. The study recommends postponing measles vaccination in the very young until this lack of understanding in the young child's immune processes are fully understood(38).
A 1987 study into a measles outbreak that occurred among adolescents in Corpus Christi, Texas, in the spring of 1985 found that the serum samples from 1806 students at two secondary schools that were obtained eight days after the onset of the first case. Only 4.1 percent of these students (74 of 1806) lacked detectable antibody to measles and more than 99 percent had records of vaccination with live measles vaccine. It was concluded that outbreaks of measles can occur in secondary schools, even when more than 99 percent of the students have been vaccinated and more than 95 percent are immune(65).
A 1994 study reports that the number of measles cases rose dramatically during the 1980s but between 20-40% of those cases occurred in persons who were adequately vaccinated. They concluded that measles had become a disease of immunised persons because of the vaccine failure rate and the unique transmissibility of the virus(39).
The defunct UK health protection agency reported failures of 40% from the meningococcal vaccine, and also reported 4 deaths that it considered as "normal". The study also acknowledges a "waning" of vaccine effectiveness that really shows that the vaccines are not necessary, because those children who were no longer protected did not catch the meningococcal virus. It also showed a spike in reported cases during 1999 when the vaccine was used most(23).
In 1999 two US Navy ships were involved in an influenza outbreak after being a high rate of vaccination. The USS California had no cases of influenza but the USS Arkansas had a 42% influenza attack rate(2)suggesting that the vaccine virus had mutated on the USS Arkansas after injection to cause the outbreak.
A 2011 study into the outbreak of measles in New York claimed to be the first study to confirm that measles can be spread to people who had been previously vaccinated twice(34). Stephen A. Krahling and Joan A. Wlochowski, former Merck virologists blew the whistle by filing a qui tam action lawsuit, U.S. v Merck & Co. The scientists alleged that the efficacy tests for the measles, mumps, rubella vaccine (MMR) were faked. This was a major federal case alleging fraud in vaccine testing by concealing study findings when they don’t reflect the desires of the cooperation concerned. it encapsulates how medical research can be manipulated to achieve desired results, and why it may be wise to question the integrity of information coming from corporations?(35).
A 2011 study found that the U.S. infant mortality rate (IMR) was higher than 33 other nations. The U.S. vaccine schedule specifies 26 vaccine doses for infants aged less than 1 year. The study used linear regression to examine the immunization schedules of these 34 nations and found a correlation between IMRs and the number of vaccine doses routinely given to infants. The study showed a high correlation between increasing number of vaccine doses and increasing infant mortality rates(64).
Another 2011 study tested 2 age groups: 6-23 months (n=100) and 24-59 months (n=100) of age for viral shedding 28 days post-vaccination. Viral shedding was detected by culture in 79% of vaccine recipients and occurred more frequently in children 6-23 months of age (89%) compared with children 24-59 months of age (69%). In total, 157 subjects shed vaccine, which was confirmed by RT-PCR as A/H1N1 for 128 subjects, A/H3N2 for 72 subjects, and B for 74 subjects. The incidence of shedding was highest on day 2 (59% in the 6-23 month age group; 41% in the 24-59 month age group) and most shedding occurred 1-11 days postvaccination(66).
A 2012 study documented that GSK were fined because 14 babies died during vaccine trials, however, the full details of the incident could not be obtained by this author because of restricted access(75).
A 2012 study investigated a mumps outbreak within a highly vaccinated university student population in the Netherlands. 776 individuals took part in the study, of whom 760 (98%) had been vaccinated at least once and 729 (94%) at least twice. The conclusion was made that high coverage of MMR vaccination in childhood did not prevent an outbreak of mumps in this student population(63).
A 2015 study explained how vaccinations interfered with natural selection and allowed highly lethal pathogens to remain living in vaccinated hosts that could then circulate within the population. It explains how immunization enhances the fitness of more virulent strains. It suggests that although vaccination prolongs the life of the host it does not prevent infection, viral replication or transmission and thus extends the infectious periods of strains otherwise too lethal to persist(77).
A 2017 study compared vaccinated and unvaccinated children on a broad range of health outcomes and aimed to determine whether an association could be found between vaccination and neurodevelopmental disorders (NDD). It found that the vaccinated were less likely than the unvaccinated to have been diagnosed with chickenpox and pertussis, but more likely to have been diagnosed with pneumonia, otitis media, allergies and NDD(71).
A 2017 study found that vaccines encouraged the dominant virus to change through the seasons to one that did not match the vaccines. It was found that vaccinated people had more mutations of the virus and their bodies became a place where the virus could mutate to become the next generation virus for the following year. Vaccines encourage virus diversity and the data suggest that in humans, immune pressure induced by vaccination works to select influenza variants genetically distant from vaccine strains(57).
Another 2017 study found that the vaccines grown on egg protein adapted to live in that environment and became less viable as a stimulator of human immune response by a factor of over x1000. It was therefore recommended that an alternative method of virus manufacture be sought(58).
Each vaccine has its dangers, a 1979 study found a link between vaccines and Guillain-Barre syndrome following vaccination. Although it found a small risk to adults it can logically be extrapolated into a larger risk for children(47).
A 2000 study found that the odds of having a history of asthma was twice as great among vaccinated subjects than among unvaccinated subjects. The odds of having had any allergy-related respiratory symptom in the past 12 months was 63% greater among vaccinated subjects than unvaccinated subjects and the associations between vaccination and subsequent allergies and symptoms were greatest among children aged 5 through 10 years. It concluded that although the number of unvaccinated cohort was small DTP or tetanus vaccination appears to increase the risk of allergies and related respiratory symptoms in adolescents(61).
A 2006 study reported a case of Rasmussen syndrome, which has a very similar profile to autism, was attributed to a vaccination(48).
A 2008 case study The case of a 3-month-old baby who dies after receiving a vaccine was studied by forensic scientists and they concluded that she died as a direct result of poisoning from the ingredients in the vaccine. How sad for the parents and how shockingly sad for that little girl to die in such a preventable way(42).
A 2009 study reported that transverse myelitis has been shown to be caused by vaccine adjuvants or undisclosed contaminants. Pain may begin suddenly in your lower back and you could have abnormal sensations. Some people with transverse myelitis reported sensations of numbness, tingling, coldness or burning. Weakness in arms or legs, bladder and bowel problems. Leaving sufferers with recurrent headaches and behavioural problems that could develop into MS after a few years(54).
A 2012 study found Pandemrix flu vaccine contributed to the onset of narcolepsy among 4 to 19 years olds during the pandemic influenza in 2009–2010 in Finland. It went on to suggest the role of the adjuvant should be considered in this event(37).
Another 2012 study used the Vaccine Adverse Event Reporting System database to establish a link between vaccination and hospitalisation. It also found the hospitalisation rate to be higher amongst the youngest and most vaccinated children(43).
Another 2012 study found vaccinated children with asthma are hospitalised 3 times more from influenza than unvaccinated children(50).
In 2013 a study was conducted by experts in Epidemiology and Surveillance of Infectious Diseases. They compared maternal antibody protection given to babies by vaccinated and unvaccinated mothers and they found that immune response are altered for generations. They concluded that children of mothers vaccinated against measles and, possibly, rubella have lower concentrations of maternal antibodies and lose protection by maternal antibodies at an earlier age than children of mothers in communities that oppose vaccination. This increases the risk of disease transmission for generations to come in highly vaccinated populations(32).
A 2014 study also found that the flu vaccine is linked to narcolepsy. The narcolepsy patients had higher median levels of A/H1N1 antibodies than the controls and the under 13-year-olds were found to have higher levels than older people and these young people had their genetic coding altered that produce Tribbles Homolog 2 that is a neuropeptide that regulates arousal, wakefulness, and appetite(36).
Another 2014 study was conducted by the "Research Center for the Study and Prevention of Unexpected Perinatal Death and SIDS" and so comes from an extremely credible source. It concludes that there is probably a direct link between vaccines and 'sudden infant deaths'(41).
A 2015 study explained that Nobel Laureate Charles Richet demonstrated over a hundred years ago that injecting a protein into animals or humans causes immune system sensitization to that protein. Subsequent exposure to the protein can result in allergic reactions or anaphylaxis. This fact has since been demonstrated over and over again in humans and animal models. The Institute of Medicine (IOM) confirmed that food proteins in vaccines cause food allergy, in its 2011 report on vaccine adverse events. The IOM’s confirmation is the latest and most authoritative since Dr. Richet’s discovery. Many vaccines and injections contain food proteins. It is well recognized that many currently approved vaccines have enough allergen to cause anaphylaxis. Therefore, they contain more than enough allergen to cause sensitization. Vaccines contain adjuvants such as pertussis toxins and aluminium compounds that also bias towards allergy. Adjuvants also increase the immunogenicity of injected food proteins. This combination of atopic children and food protein injection along with adjuvants, contributes to millions developing life-threatening food allergies. Given the scale and severity of the food allergy epidemic, urgent action is needed to change vaccine policy concerning vaccine specifications, manufacture, vaccine package insert documentation requirements(70).
A 2017 study reported that 'sudden infant deaths' are not recorded using consistent guidelines and those investigations into the cause of death are not thorough enough to ascertain the involvement of vaccination. This inadequacy of the system leaves the possibility that many more deaths due to vaccination occur than are actually recorded(40).
A 2017 study into the 2011-2012 influenza vaccine concluded that it could cause spontaneous abortions in women who had received an H1N1 vaccine the previous year 2010-2011 and suggested further research is warranted(67).
A 2017 study found that children who received diphtheria-tetanus-pertussis (DTP) and oral polio vaccine (OPV) between 3 and 5 months of age had a 5-fold higher mortality than still unvaccinated children and concluded that DTP was associated with increased mortality and OPV may modify the effect of DTP(69).
A 2017 study found animal protein sequences exactly match human proteins except for occasional amino acid differences and T cells can become autoreactive when they are activated by a peptide that exactly matches a self-peptide except for this one amino acid difference. Ingested animal proteins are immunologically processed to produce a tolerogenic response. Injected animal proteins are however another matter. Animal cells and proteins are used as growth media for the culture of viruses and bacteria, and as excipients in the manufacture of vaccines. Such vaccines are contaminated with numerous animal proteins. When animal proteins are injected with vaccines that either contain live viruses or adjuvants that provoke an immune response, T cells can be activated by peptides derived from these animal proteins thus resulting in autoimmunity(68).
Another 2017 study highlights the failure of the polio vaccine and declares that “poliovirus eradication is hampered globally by epidemics of vaccine-derived polio”. It goes on to say that “mutations accumulating during epidemics increase the replication fitness of the virus” and “increase virulence”. The study “uncovers the evolutionary strategies by which vaccine strains become pathogenic”(55).
A 2018 epidemiological study into birth rates and the HPV vaccine examined data from nearly 8 million women and found a decline in birth rates amongst women aged 25-29, at the peak of their childbearing years in the United States since 2007. The data came from the CDC who started their database in 1995 and eliminated possible influences associated with these changes in birth rates by examining responses to the National Health and Nutrition Examination Survey, the demographic and socio-economic information and race and ethnicity. It also matched the sample groups for age and marriage/relationship status. It found that births were significantly lower in all groups and concluded that “Several case studies link the HPV shot to Premature Ovarian Failure, suggesting one mechanism through which the vaccine affected fertility might involve ovarian damage”. It went on to explain “approximately 60% of women who did not receive the HPV vaccine had been pregnant at least once, whereas only 35% of women who were exposed to the vaccine had ever conceived”. It suggests that vaccine side effects have been missed and that more studies need to be made into the fertility issues of the HPV vaccine. It went on to say that if all females had been vaccinated the US birth rate would have fallen by 2 million(24).
Another 2018 study reported a very small fraction of people can develop Guillain–Barre syndrome due to vaccines and vaccinations like a meningococcal vaccine, poliovirus vaccine, influenza vaccine, and rabies vaccine. Of all these, rabies is invariably fatal. It can be preventable if diagnosed early and post-exposure treatment is followed according to the World Health Organization guidelines. Older formulations of rabies vaccines are cultured in the neural tissues and have been found to have an increased risk of Guillain–Barre syndrome. Although less immunogenic older formulations of rabies vaccines are more commonly used in Asian and South American countries due to their cost-effective nature. There is little to no data available on the incidence of Guillain–Barre syndrome due to vaccinations in Pakistan. Most of the cases of Guillain–Barre syndrome due to vaccination are either undiagnosed or misdiagnosed(46).
A 2019 study found that the effectiveness of the BCG vaccine was not satisfactory and this was said to be because of variations in batch quality. The study concluded that vaccination with a live virus entrained the body’s immune system whereby vaccination with an inactivated vaccine like DTP repressed the innate immune response and this was found to be associated with overall illness and higher death rates(31).
In 2019 it was reported in The Times online, that the Cancer pioneer Martin Gore died of sudden organ failure after a routine vaccination for yellow fever(49).
The vitamin K vaccination was studied in 1959 and concluded that the Oral Vitamin K was shown to be as effective as the injected form(52).
A 1998 study by The Journal of the Royal College of Paediatrics and Child Health advise that Vitamin K drops are adequate and effective. The study explains that the vitamin K muddle has already gone on for too long and suggests that it is brought to an end by developing a daily drop preparation and adopting, for all normal risk breast fed infants, the regimen that has served so well in the Netherlands. Rates of VKDB should be lower than at present and any possibility, however remote, of prophylaxis harming some normal risk infants will be removed(44).
A 2003 study also confirmed the effectiveness of Vitamin K drops but unfortunately reported that Roche withdrew the currently used Konakion multidose dropper bottle preparation (phytomenadione, the original cremaphor preparation) from the Danish market, without any explanation. At present, no licensed oral preparation is available in Denmark(45).
A 2017 study analysed recent literature data and found that oral administration of three doses of 2mg of vitamin K1 at birth, at discharge from the maternity ward, and at 1 month postnatal age for term infants would be appropriate treatment to combat haemorrhagic disease(53).
Contaminates found using electron-microscopy investigation into vaccines found many different forms of solid nanosized particles after drying. These contaminates were not declared among the list of ingredients and their presence is inexplicable. The evidence collected suggests a correlation between human diseases and vaccine contaminants. Forty four types of vaccines from Italy and France were examined but the same vaccines are used in every country throughout the world. Aluminium, Antimony, Bismuth, Bromine, Calcium particles, Cerium, Chlorine, Chromium, Gold, Hafnium, Iron, Lead, Magnesium, Nickel, Platinum, Potassium, Silicon, Silver, stainless steel, Strontium, Titanium, Tungsten, Zinc and Zirconium as well as proteins, endotoxins, red blood cells and residues of bacteria. These particles have no technical use and a reason for their inclusion cannot be found in any material handbook. Therefore, they should not be present in any injectable medicine, let alone in vaccines, especially vaccines meant for children(56).
Vaccine industry secrets where exposed 2008 study exposed the duplicity of the pharmaceutical industry by explaining how a secret meeting was convened to discuss the link between autism and heavy metal poisoning from vaccines. The meeting was Attended by 51 scientists, representatives of pharmaceutical vaccine manufacturing companies and a representative of the World Health Organization. However, accepted experts in the field of mercury neurotoxicity were excluded from the meeting. Dr. Verstraeten’s study was discussed, which looked at the data from the Vaccine Safety Datalink and found a significant correlation between Thimerosal exposure via vaccines and several neurodevelopmental disorders including tics, speech and language delays, and possibly ADD. To disguise this link another data set was included to negate the findings(74).
The CDC admit that the contamination of vaccines with SV40 from monkeys causes cancer but they have since removed the page from their website, however, it is available for view here.
We are told Herd Immunity needs 95% vaccination coverage is necessary to be established but the original observations by Hedrich only suggested 68% of natural immunity is needed to establish "herd immunity"(82). The definition of "herd immunity" that the vaccine companies use comes from a model called the REED- FROST model but the model is flawed because there are many parameters that are impossible to account for, especially when dealing with children of school age(83).
Furthermore, a book written in 1889 called "45 years of Registration Statistics, Proving Vaccination to be both useless and dangerous". It covers 45 years (starting in the year 1844) and examines the statistics of vaccine failures including an increase in death from other diseases, once the blood has been poisoned by vaccination. They cover the health of the vaccinated versus the unvaccinated and found the vaccinated were dying more from other diseases such as measles, mumps, smallpox and diphtheria because of a weakened immune system from vaccines(84).
Should we be forced to vaccinate? Merck advises on page 1306 of their manual that written consent should be obtained after full disclosure of the adverse effects of vaccination(33). It is therefore surprising that Governments intend to make vaccines mandatory, especially after the disasters of the past that resulted from vaccination programs. The effectiveness of sanitation to control disease is overlooked by the vaccine industry even though we have evidence of the role of sanitation in propagating the spread of disease when we consider todays third world countries. We also have evidence of the changes good sanitation and clean drinking water made during the early 1900s in the developed countries of the western world. This was documented on pages 21 -24 of ‘The Horrors of Vaccination’ when it examines Leicester England during the early 1900s, where no compulsory vaccination program existed for over 30 years previously. Death rates fell amongst the 300,000 inhabitants of Leicester faster during this time than elsewhere because of sanitation and not because of the ongoing vaccine program that was being promoted in other places(4).
The hippocratic oath encourages that we always have the patients best interest in mind and we do not treat healthy patients unnecessarily. The medical profession also has the moto Primum non nocere whichtranslates to “first do no harm”.
In 2017 The Swedish Parliament upheld these values when it said no to all motions on public health issues that require mandatory vaccinations(51).
Conclusions
It has been shown how the media and governments are being used by vaccine corporations to control the understanding of the dangers that vaccination brings and how the vaccine industry operates in secret through fear of the general public discovering that injecting poisons directly into the body represents a danger.
It has been shown that the controlling bodies and health agencies who we believe protect the general public’s interests in an unbiased way are in fact subsidiaries of the vaccine corporations.
It has been shown that even though the vaccine companies vehemently deny any connection between vaccines and autism the mechanism of mitochondrial dysfunction is well understood and the role that vaccines play in it is very apparent.
The danger of all adjuvants is recognised and have been shown to result in long term degenerative neurological complaints and are also considered to be responsible for the increase in developed food allergies as well as an overall reduction in health that leaves a person more susceptible to other illnesses.
Vaccinations produce sensitisation to the vaccine ingredients that include food and animal proteins, they do not produce immunity. If vaccines supplied immunity in the normal way it would only be necessary to have one vaccine for each disease and that immunisation would last their whole lifetime
The failures of vaccinations has been documented and in many cases only the vaccine version of the disease exists in the population. It has been shown that vaccine failures are commonplace and that vaccines spread disease through shedding.
The dangers that vaccinations bring in the form of adverse effects has also been established and these adverse effects are often serious enough to result in death or life-long disabilities.
It has been shown that injecting new-born babies damages their neurological development and is not necessary in most cases, especially when considering Vitamin K that can be given effectively in oral drop form and hepatitis B when a child is unlikely to be in a position to contract this blood born disease unless the breast feeding Mother already has hepatitis B.
Undisclosed contaminants were found in vaccines and these contaminants have no purpose and can cause drastic consequences for the recipient that may result in cancer and death.
It has been shown that the vaccine industry cannot be trusted to be completely open and honest and in fact it has been shown that they commonly hide information that is to their detriment.
We are told that “herd Immunity” is necessary and this idea drives the call for everyone to vaccinate but even though the 95% coverage recommended by the vaccine industry for herd immunity is wrong it can never be established because of the vast amount of vaccine failures.
Mandatory vaccination is unconstitutional and goes against every medical ethic. It has been suggested by Merck that adults and parents should give written consent before vaccination and this permission should only be solicited after all of the adverse effects have been explained in full and understood completely by the patient. Mandatory vaccination has been tried many times in the past and has always resulted in many deaths and permanent ill-health of the vaccinated because every vaccine is inherently unsafe(85) due to the normal manufacturing processes.
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