144 vaccine sources from

For those wanting “legit” sources on vaccines here’s 144 .Gov studies/links.

Have more? Add them below!

1. Here's the ingredients straight from the CDC website. You’ll see 440 different ingredients, including fetal cell lines, human albumin derived from human blood, genetically engineered human albumin derived from yeast, animal cells or serum (cow, guinea pig, dog, chick, pig, monkey, worm), aluminum, thimerosol, polysorbate 80, borax, yellow 5, MSG, formaldehyde, aluminum phosphate, latex, phenol and more. https://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/B/excipient-table-2.pdf

2. In the US, if you or your child are harmed by vaccines you cannot sue the manufacturer. You can file a claim with the National Vaccine Injury Compensation Program for $400 and hope to prove that the injury was caused by the vaccine. This is a very challenging thing to do, yet to date the program has paid out more than $3.6 Billion in claims.

The National Vaccine Injury Compensation Program is a no-fault alternative to the traditional legal system for resolving vaccine injury petitions. It was created in the 1980s, after lawsuits against vaccine companies and health care providers threatened to cause vaccine shortages and reduce U.S. vaccination rates, which could have caused a resurgence of vaccine preventable diseases. Any individual, of any age, who received a covered vaccine and believes he or she was injured as a result, can file a petition. Parents, legal guardians and legal representatives can file on behalf of children, disabled adults, and individuals who are deceased." https://www.hrsa.gov/vaccinecompensation/

3. FDA.gov - Every vaccine package insert has a section, 13.1, which says essentially "this vaccine has not been tested for teratogenic or mutagenic effects". So the vaccine has not been tested to see if it will cause cancer but the ingredients have. We know formaldehyde is carcinogenic. We know polysorbate 80 is carcinogenic. We know aluminum is a neurotoxin... There is one exception. Varicella (chicken pox). There is no section 13 in the Varicella package insert (PI). The PI jumps from 12 to 14. Where did 13 go? If the PI doesn't explicitly say the vaccine hasn't been tested for carcinogenic effects is it because it HAS been tested? Where are the results? Why aren't they disclosed?

4. The two strains of aborted fetal tissue that are used now in the United States are WI38 and MRC5, developed using an aborted female and an aborted male in the 1960’s. They can only be replicated for so long, as fetal cells are highly tumorigenic (prone to cancer). There is a “need” to develop new fetal cell lines to develop new vaccines. A newer fetal cell line has been developed in China, Walvax2. There were nine abortions that went into the development of that cell line. Those babies were delivered by water bag method, so that all of the organs would be intact. These babies are often delivered alive – up to 20 weeks old in some cases. It’s not two abortions that were done “A long time ago.” This is an ongoing thing. The manipulation and greed involved in this is extreme. '" https://www.ncbi.nlm.nih.gov/m/pubmed/25803132/

5. http://www.uscfc.uscourts.gov/opinion-search 174 claims from the MMR vax in us courts, found by searching "measles"

6. Look at P41 https://www.cdc.gov/nchs/data/nvsr/nvsr65/nvsr65_04.pdf Here's CDC data to compare it to. https://www.cdc.gov/nchs/data_access/Vitalstatsonline.htm

7. Shows that measles was already in decline by the time the vaccine came out. https://www.cdc.gov/vaccines/pubs/pinkbook/meas.html

8. So I did some digging and math and the flu shots contain a LOT of thimerosal The 2017-18 Influenza vaccines have been approved for use and will contain Thimerosal (Hg, mercury) and are recommended for every child, adult and pregnant mother. Here are the 5 different influenza vaccines:

Trivalent Influenza Vaccine, Afluria (multi-dose presentation) Seqirus Pty Ltd 0.01% (24.5 mcg/-One 0.5 mL dose jab will contain 24.5 mcg = 24,500 ppd

Fluvirin multi dose, 0.5 mL one dose prefilled syringe will contain ≤ 1 Hg 5.0 mL multi-dose vial—one 0.5 mL jab will contain 25mcg = 25,000 ppb

Fluvirin (single-dose presentation) Seqirus Vaccines Ltd Trace (<1 mcg/0.5mL)

Quadrivalent Influenza Vaccine Afluria Quadrivalent (multi-dose presentation) Seqirus Pty Ltd 0.01% (24.5 mcg/0.5 mL dose) One 0.5 mL dose jab will contain 24.5 mcg = 24,500 ppd

FluLaval Quadrivalent (multi-dose presentation) vID Biomedical Corporation of Quebec 0.01% (25 mcg/0.5 mL dose)2 One 0.5 mL dose jab will contain 25 mcg = 25,000 ppd

Fluzone Quadrivalent (multi-dose presentation) Sanofi Pasteur Inc. 0.01% (12.5 mcg/0.25 mL dose, 25 mcg/0.5 mL dose) One 0.5 mL dose jab will contain 25 mcg = 25,000 pp

Please keep in mind that one (1) microgram equals 0.0010 milligram (mg). Often physicians refer to the “trace” of thimerosal as safe and even healthy! The way to compare what a trace is in a vaccine is to compare to what is considered safe and allowable in our environment: water, liquids and foods we eat and compare the levels in the vaccines they encourage us to inject.

2 ppb (parts-per-billion) is the mandated safety limit in drinking water

• 0.5 parts per billion (ppb) mercury = Kills human neuroblastoma cells (Parran et al., Toxicol Sci 2005; 86: 132-140). • 2 ppb mercury = U.S. EPA limit for drinking water. • 20 ppb mercury = Neurite membrane structure destroyed (Leong et al., Neuroreport 2001; 12: 733-37). • 200 ppb mercury = level in liquid the EPA classifies as hazardous waste. • 24,500 ppb Mercury = Current "preservative" level mercury in multi-dose flu This can be confirmed by simply analyzing the multi- dose vials. https://www.fda.gov/…/SafetyAvailab…/VaccineSafety/UCM096228

9. Section 11 Flublok insert https://www.fda.gov/…/Vaccin…/ApprovedProducts/UCM336020.pdf

10.Flu outbreak in vaccinated https://www.cdc.gov/mmwr/preview/mmwrhtml/mm6342a3.htm

11. The story starts when the Canadians noticed in 2010 that the people who got annual flu shots were getting the pandemic strain A/H1N1-pdm09 more often than the people who got no shot at all: Seasonal Influenza Vaccine and Increased Risk of Pandemic A/H1N1-Related Illness: First Detection of the Association in British Columbia, Canada�https://www.ncbi.nlm.nih.gov/pubmed/20887210 Other groups found the same thing and this led to a 2014 study with ferrets that replicated the effect, thereby showing that the observations were sound: Randomized Controlled Ferret Study to Assess the Direct Impact of 2008–09 Trivalent Inactivated Influenza Vaccine on A(H1N1)pdm09 Disease Risk�http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3903544 While this was happening in Canada, the Chinese became curious and this 2012 study from the University of Hong Kong showed that the children had a 4.4 higher chance of getting an upper respiratory virus infection after getting the seasonal flu shot: Increased Risk of Noninfluenza Respiratory Virus Infections Associated With Receipt of Inactivated Influenza Vaccine�http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3404712/

12. Flu outbreak in vaccinated https://www.cdc.gov/mmwr/preview/mmwrhtml/mm6342a3.htm

13. Annual Vaccination against Influenza Virus Hampers Development of Virus-Specific CD8+ T Cell Immunity in Children�https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3209321/

14. The two faces of heterologous immunity: protection or immunopathology�https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923083

15. Influenza vaccination: policy versus evidence, BMJ, October 2006�http://www.ncbi.nlm.nih.gov/pubmed/17068038

16. www.ncbi.nlm.nih.gov/pmc/articles/PMC4387051/ Repeated flu shot may blunt effectiveness

17. Our results show that: (i) children from countries with the highest autism spectrum disorder (ASD) prevalence appear to have the highest exposure to aluminum from vaccines; (ii) the increase in exposure to aluminum adjuvants significantly correlates with the increase in ASD prevalence in the United States observed over the last two decades; and (iii) a significant correlation exists between the amounts of aluminum administered to preschool children and the current prevalence of ASD in seven Western countries. http://www.ncbi.nlm.nih.gov/pubmed/22099159

18. Vaccines caused autism here in this federal court case http://www.uscfc.uscourts.gov/…/opin…/ABELL.ZELLER073008.pdf And here page 2 http://www.uscfc.uscourts.gov/…/CAMPBELL-SMITH.MOJABI-PROFF… And here - https://ecf.cofc.uscourts.gov/cgi-bin/show_public_doc…

Here are 83 cases reviewed by lawyers http://digitalcommons.pace.edu/cgi/viewcontent.cgi…

Oh look here's a dead kid compensated https://ecf.cofc.uscourts.gov/cgi-bin/show_public_doc…

19. Supreme Court Unavoidably Unsafe http://www.supremecourt.gov/opinions/10pdf/09-152.pdf

20. Check out the CDC website to see descriptions of all the vaccine preventable diseases along with the number of cases and deaths each year. You'll find they aren't as serious as were led to believe and not deadly in healthy individuals.

21. A dose-response relationship between organic mercury exposure from thimerosal-containing vaccines and neurodevelopmental disorders. http://www.ncbi.nlm.nih.gov/pubmed/25198681

22. Relative trends in hospitalizations and mortality among infants by the number of vaccine doses and age, based on the Vaccine Adverse Event Reporting System (VAERS), 1990-2010. http://www.ncbi.nlm.nih.gov/pubmed/22531966

23. Is infant immunization a risk factor for childhood asthma or allergy? http://www.ncbi.nlm.nih.gov/pubmed/9345669

24. Infant mortality rates regressed against number of vaccine doses routinely given: Is there a biochemical or synergistic toxicity? http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170075/

25.Infection, vaccines and other environmental triggers of autoimmunity. http://www.ncbi.nlm.nih.gov/pubmed/16126512

26. DTP with or after measles vaccination is associated with increased in-hospital mortality in Guinea-Bissau. http://www.ncbi.nlm.nih.gov/pubmed/17092614#

27. Measles outbreak in a vaccinated school population: epidemiology, chains of transmission and the role of vaccine failures. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1646939/

28. A positive association found between autism prevalence and childhood vaccination uptake across the U.S. population. http://www.ncbi.nlm.nih.gov/pubmed/21623535

29. Hepatitis B vaccination of male neonates and autism diagnosis, NHIS 1997-2002. http://www.ncbi.nlm.nih.gov/pubmed/21058170

30. Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism. http://www.ncbi.nlm.nih.gov/pubmed/12145534

31. The plausibility of a role for mercury in the etiology of autism: a cellular perspective http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3173748/

32.-54. Published studies from .gov sites which show vaccines cause Autism.

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878266/ http://www.ncbi.nlm.nih.gov/pubmed/21623535 http://www.ncbi.nlm.nih.gov/pubmed/25377033 http://www.ncbi.nlm.nih.gov/pubmed/24995277 http://www.ncbi.nlm.nih.gov/pubmed/12145534 http://www.ncbi.nlm.nih.gov/pubmed/21058170 http://www.ncbi.nlm.nih.gov/pubmed/22099159 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/ http://www.ncbi.nlm.nih.gov/pubmed/17454560 http://www.ncbi.nlm.nih.gov/pubmed/19106436 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3774468/ http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3697751/ http://www.ncbi.nlm.nih.gov/pubmed/21299355 http://www.ncbi.nlm.nih.gov/pubmed/21907498 http://www.ncbi.nlm.nih.gov/pubmed/11339848 http://www.ncbi.nlm.nih.gov/pubmed/17674242 http://www.ncbi.nlm.nih.gov/pubmed/21993250 http://www.ncbi.nlm.nih.gov/pubmed/15780490 http://www.ncbi.nlm.nih.gov/pubmed/12933322 http://www.ncbi.nlm.nih.gov/pubmed/16870260 http://www.ncbi.nlm.nih.gov/pubmed/19043938 http://www.ncbi.nlm.nih.gov/pubmed/12142947 http://www.ncbi.nlm.nih.gov/pubmed/24675092

55. Here is your reference for just 0.3% of the aluminum that is ingested getting to the blood. The ATSDR cites 0.01% to 5% (see link) and a common value used in aluminum ingestion studies is 0.3%. That's not 3%—it's zero point 3 percent.

When someone tells you that we ingest more aluminum than we get from vaccines, they never multiply by 0.003 thus their argument is entirely false.

ToxGuide(tm) for Aluminum, Agency for Toxic Substances and Disease Registry https://www.atsdr.cdc.gov/toxguides/toxguide-22.pdf

56. Effects of diphtheria-tetanus-pertussis or tetanus vaccination on allergies and allergy-related respiratory symptoms among children and adolescents in the United States. http://www.ncbi.nlm.nih.gov/pubmed/10714532

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 The associations between vaccination and subsequent allergies and symptoms were greatest among children aged 5 through 10 years.

57. Neurological Complications of Pertussis Immunization http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2025848/…

Review is made of 107 cases of neurological complications of pertussis inoculation reported in the literature. The early onset of neurological symptoms was characteristic, with changes of consciousness and convulsions as the most striking features. The question of aetiology is considered and contraindications are discussed....as is the grave danger of further inoculations when a previous one has produced any suggestion of a neurological reaction.

58. Pertussis in vaccinated https://wwwnc.cdc.gov/eid/syn/en/article/22/2/15-0325.htm

59. Rotovirus sheds causing contagion: http://www.ncbi.nlm.nih.gov/pubmed/18922486 This vaccine doesn’t appear to do anything more than what nature would do with this virus naturally; except, the vaccine has shedding of the Rotavirus https://www.ncbi.nlm.nih.gov/pubmed/24582311

60. RotaTeq vaccine Insert- http://www.merck.com/…/pi_circulars/r/rotateq/rotateq_pi.pdf Check out the Rotavirus vaccine insert. Please review page 5, this page covers the clinic trial of the Rotavirus vaccine. Please note “Deaths Across the clinical studies, 52 deaths were reported. The most commonly reported cause of death was sudden infant death syndrome, which was observed in 8 recipients of RotaTeq and 9 placebo recipients.” Why? Because their placebo vaccines have adjuvants in them. (page 10) “Pediatric Use: Safety and efficacy have not been established in infants less than 6 weeks of age or greater than 32 weeks of age.”(page 1 of insert) All children in the study were over 8 months old; however, the CDC schedule recommends vaccination at 2 to 6 months.

Post marketing results from vaccine: Immune system disorders: Anaphylactic reaction, Gastrointestinal disorders: Intussusception (including death) Hematochezia Gastroenteritis with vaccine viral shedding in infants with Severe Combined Immunodeficiency Disease (SCID) Skin and subcutaneous tissue disorders: Urticaria Angioedema Infections and infestations: Kawasaki disease.

According to the CDC here are the risk of Rotavirus yearly. More than 400,000 doctor visits more than 200,000 emergency room visits, 55,000 to 70,000 hospitalizations, and 20 to 30 deaths (notice that 52 deaths occurred in the trial? That is out of 71,725 infants)

Now go to page 10 and look at the clinical trials; the 73,086 infants were randomized and conducted in 12 countries that is really under 6,000 participants in each country. I’m not a genius but don’t different countries have different sanitation, environment, and economic conditions that play a role in disease? “Overall, 73,086 infants were randomized in 4 placebo-controlled, phase 3 studies conducted in 12 countries on 4 continents.”

"Rotateq has not been evaluated for its carcinogenic or mutagenic potential or its potential to impair fertility."

61. According to the CDC here are the risk of Rotavirus yearly. More than 400,000 doctor visits more than 200,000 emergency room visits, 55,000 to 70,000 hospitalizations, and 20 to 30 deaths (notice that 52 deaths occurred in the trial? That is out of 71,725 infants) Rotavirus surveillance : https://www.cdc.gov/rotavirus/surveillance.html

62. Natural history of Rotavirus : https://www.ncbi.nlm.nih.gov/pubmed/9015109

63. Rotavirus information: https://www.cdc.gov/vaccin…/pubs/pinkbook/downloads/rota.pdf

64. The FDA limits aluminum in parenteral solutions at 4-5 mcg/kg/day. Due to the fact that no safe limit for injecting aluminum via vaccine has *ever* been scientifically determined, this is the limit we have to reference when looking at the issue of aluminum in vaccines.

https://www.accessdata.fda.gov/…/cfdocs/cfcfr/CFRSearch.cfm…

So if the FDA limit is 5mcg/kg/day and the average 2 month old weighs around 5kg, the limit is 25mcg/day.

You can check the manufacturer website for the content of aluminum in vaccines.

65. Aluminum adjuvant linked to Gulf War illness induces motor neuron death in mice. http://www.ncbi.nlm.nih.gov/pubmed/17114826 The findings suggest a possible role for the aluminum adjuvant in some neurological features associated with GWI and possibly an additional role for the combination of adjuvants (Synergistic Toxicity).

66. Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity. http://www.ncbi.nlm.nih.gov/pubmed/23609067

67. Biopersistence and brain translocation of aluminum adjuvants of vaccines. http://www.ncbi.nlm.nih.gov/pubmed/25699008 We previously showed that poorly biodegradable aluminum-coated particles injected into muscle are promptly phagocytosed in muscle and the draining lymph nodes, and can disseminate within phagocytic cells throughout the body and slowly accumulate in brain. This strongly suggests that long-term adjuvant biopersistence within phagocytic cells is a prerequisite for slow brain translocation and delayed neurotoxicity.

68. Autoimmune/inflammatory syndrome induced by adjuvants (Shoenfeld's syndrome): clinical and immunological spectrum. http://www.ncbi.nlm.nih.gov/pubmed/23557271 The activation of the immune system by adjuvants, a desirable effect, could trigger manifestations of autoimmunity or autoimmune disease. Recently, a new syndrome was introduced, autoimmune/inflammatory syndrome induced by adjuvants (ASIA), that includes postvaccination phenomena, macrophagic myofasciitis, Gulf War syndrome and siliconosis. This syndrome is characterized by nonspecific and specific manifestations of autoimmune disease. The main substances associated with ASIA are squalene (Gulf War syndrome), aluminum hydroxide (postvaccination phenomena, macrophagic myofasciitis) and silicone with siliconosis. Mineral oil, guaiacol and iodine gadital are also associated with ASIA.

69. The FDA limits aluminum in parenteral solutions at 4-5 mcg/kg/day. Due to the fact that no safe limit for injecting aluminum via vaccine has *ever* been scientifically determined, this is the limit we have to reference when looking at the issue of aluminum in vaccines.

https://www.accessdata.fda.gov/…/cfdocs/cfcfr/CFRSearch.cfm…

So if the FDA limit is 5mcg/kg/day and the average 2 month old weighs around 5kg, the limit is 25mcg/day.

You can check the manufacturer website for the content of aluminum in vaccines.

70. Published in the International Journal of Pharmaceutics, 2014: Evaluation of synergistic effect of biodegradable polymeric nanoparticles and aluminum based adjuvant for improving vaccine efficacy. source: http://www.ncbi.nlm.nih.gov/pubmed/24939616

71. Mechanisms of aluminum adjuvant toxicity and autoimmunity in pediatric populations.

http://www.ncbi.nlm.nih.gov/pubmed/22235057 Immune challenges during early development, including those vaccine-induced, can lead to permanent detrimental alterations of the brain and immune function. Experimental evidence also shows that simultaneous administration of as little as two to three immune adjuvants can overcome genetic resistance to autoimmunity. In some developed countries, by the time children are 4 to 6 years old, they will have received a total of 126 antigenic compounds along with high amounts of aluminum (Al) adjuvants through routine vaccinations. According to the US Food and Drug Administration, safety assessments for vaccines have often not included appropriate toxicity studies because vaccines have not been viewed as inherently toxic. Taken together, these observations raise plausible concerns about the overall safety of current childhood vaccination programs. When assessing adjuvant toxicity in children...

72. Aluminum adjuvant linked to Gulf War illness induces motor neuron death in mice. http://www.ncbi.nlm.nih.gov/pubmed/17114826 The findings suggest a possible role for the aluminum adjuvant in some neurological features associated with GWI and possibly an additional role for the combination of adjuvants (Synergistic Toxicity).

73. Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity. http://www.ncbi.nlm.nih.gov/pubmed/23609067

74. Biopersistence and brain translocation of aluminum adjuvants of vaccines. http://www.ncbi.nlm.nih.gov/pubmed/25699008 We previously showed that poorly biodegradable aluminum-coated particles injected into muscle are promptly phagocytosed in muscle and the draining lymph nodes, and can disseminate within phagocytic cells throughout the body and slowly accumulate in brain. This strongly suggests that long-term adjuvant biopersistence within phagocytic cells is a prerequisite for slow brain translocation and delayed neurotoxicity.

75. Autoimmune/inflammatory syndrome induced by adjuvants (Shoenfeld's syndrome): clinical and immunological spectrum. http://www.ncbi.nlm.nih.gov/pubmed/23557271 The activation of the immune system by adjuvants, a desirable effect, could trigger manifestations of autoimmunity or autoimmune disease. Recently, a new syndrome was introduced, autoimmune/inflammatory syndrome induced by adjuvants (ASIA), that includes postvaccination phenomena, macrophagic myofasciitis, Gulf War syndrome and siliconosis. This syndrome is characterized by nonspecific and specific manifestations of autoimmune disease. The main substances associated with ASIA are squalene (Gulf War syndrome), aluminum hydroxide (postvaccination phenomena, macrophagic myofasciitis) and silicone with siliconosis. Mineral oil, guaiacol and iodine gadital are also associated with ASIA.

76. Long-term Persistence of Vaccine-Derived Aluminum Hydroxide is Associated with Chronic Cognitive Dysfunction http://www.sciencedirect.com/…/article/pii/S0162013409001895

77. Long-term follow-up of cognitive dysfunction in patients with aluminum hydroxideinduced macrophagic myofasciitis (MMF). http://www.sciencedirect.com/…/article/pii/S0162013411002194

78. Why is Aluminum being used as an adjuvant in vaccines when there are many .gov studies against it's use as Toxic? (Go to Section 1.2. The Toxic Effects of Aluminum as a Vaccine Adjuvant. One of many Al studies) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202242/

79. How clean water help stop the spread of disease https://www.cdc.gov/healthywater/drinking/history.html

80. page from the CDC website themselves showing stats about water treatment plants being built, vaccines being introduced, and the decline of diseases. And secular trends in the US https://www.cdc.gov/vaccines/pubs/pinkbook/meas.html

81. SIDS http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170075/

82. History of Infant Mortality Rates http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170075/…

83.SIDS after hexavalent vaccine http://www.ncbi.nlm.nih.gov/pubmed/18538957

84. Infant mortality and vaccine schedule http://www.ncbi.nlm.nih.gov/…/PMC…/pdf/envhper00326-0221.pdf

85.?Adverse effects on vaccinating premies http://www.ncbi.nlm.nih.gov/…/articl…/PMC2082954/table/tbl2/

86. Infant mortality and vaccines study http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170075/

87. Both twins die after vaccines http://www.ncbi.nlm.nih.gov/pubmed/17654772

88. Autism and SIDS just a coincidence Autism package insert says DTaP (Tripedia) lists Autism and SIDS as a side effect in their package insert!!

‘Adverse events reported during post-approval use of Tripedia vaccine include idiopathic thrombocytopenic purpura, SIDS, anaphylactic reaction, cellulitis, autism, convulsion/grand mal convulsion, encephalopathy, hypotonia, neuropathy, somnolence and apnea. Events were included in this list because of the seriousness or frequency of reporting.’ http://www.fda.gov/…/Vaccines/ApprovedProducts/ucm101580.pdf

89. Aluminum http://www.fda.gov/ohrms/dockets/98fr/oc0367.pdf

90. https://www.fda.gov/ohrms/dockets/98fr/oc0367.pdf

The package inserts have the amounts in the description section. If you convert the numbers from mg to mcg, the numbers match.

91. Thimerosol & Vaccines https://www.fda.gov/…/SafetyAvailab…/VaccineSafety/UCM096228

92. https://www.cdc.gov/vaccines…/concerns/thimerosal/index.html

93. Understanding mercury https://www.cdc.gov/…/d…/vacsafe-thimerosal-color-office.pdf

94. Mercury in Healthcare https://www.novascotia.ca/…/pollutionprevention/docs/Mercur…

95. Thimerosal studies:

Integrating experimental (in vitro and in vivo) neurotoxicity studies of low-dose thimerosal relevant to vaccines. http://www.ncbi.nlm.nih.gov/pubmed/21350943

There is a need to interpret neurotoxic studies to help deal with uncertainties surrounding pregnant mothers, newborns and young children who must receive repeated doses of Thimerosal-containing vaccines (TCVs).

Information extracted from studies indicates that: (a) activity of low doses of Thimerosal against isolated human and animal brain cells was found in all studies and is consistent with Hg neurotoxicity; (b) the neurotoxic effect of ethylmercury has not been studied with co-occurring adjuvant-Al in TCVs; (c) animal studies have shown that exposure to Thimerosal-Hg can lead to accumulation of inorganic Hg in brain, and that (d) doses relevant to TCV exposure possess the potential to affect human neuro-development.

96. Neurodevelopmental disorders following thimerosal-containing childhood immunizations: a follow-up analysis. http://www.ncbi.nlm.nih.gov/pubmed/15764492

“The present study provides additional epidemiological evidence supporting previous epidemiological, clinical and experimental evidence that administration of thimerosal-containing vaccines in the United States resulted in a significant number of children developing NDs.”

97. Neonatal administration of thimerosal causes persistent changes in mu opioid receptors in the rat brain http://www.ncbi.nlm.nih.gov/pubmed/20803069

“These data document that exposure to thimerosal during early postnatal life produces lasting alterations in the densities of brain opioid receptors along with other neuropathological changes, which may disturb brain development.”

98. Persistent behavioral impairments and alterations of brain dopamine system after early postnatal administration of thimerosal in rats. http://www.ncbi.nlm.nih.gov/pubmed/21549155

“These data document that early postnatal THIM administration causes lasting neurobehavioral impairments and neurochemical alterations in the brain, dependent on dose and sex. If similar changes occur in THIM/mercurial- exposed children, they could contribute do neurodevelopmental disorders.”

99. Maternal Thimerosal Exposure Results in Aberrant Cerebellar Oxidative Stress, Thyroid Hormone Metabolism, and Motor Behavior in Rat Pups; Sex- and Strain-Dependent Effects. http://www.ncbi.nlm.nih.gov/pubmed/22015705

Thimerisol exposure also resulted in a significant increase in cerebellar levels of the oxidative stress marker 3-nitrotyrosine.... This coincided with an increased (47.0%) expression of a gene negatively regulated by T3,... Our data thus demonstrate a negative neurodevelopmental impact of perinatal thimerisol exposure.

100. Administration of thimerosal to infant rats increases overflow of glutamate and aspartate in the prefrontal cortex: protective role of dehydroepiandrosterone sulfate. http://www.ncbi.nlm.nih.gov/pubmed/22015977

Thimerosal, a mercury-containing vaccine preservative, is a suspected factor in the etiology of neurodevelopmental disorders. We previously showed that its administration to infant rats causes behavioral, neurochemical and neuropathological abnormalities similar to those present in autism.

101. We always hear how ethyl mercury is a "non toxic" form of mercury. The FDA itself says the opposite.

Page 407:

https://www.fda.gov/…/07p-0331-cp00001-006-(47-pages)-vol1.…

“Although thimerosal is an ethyl mercury compound, it has similar toxicological properties to methyl mercury and the long-term neurological sequelae, produced by the ingestion of either methyl or ethyl mercury-based fungicides, are indistinguishable.“

102. Herd immunity did not stop an outbreak in Quebec. “The vaccination coverage among cases was at least 84.5%. Vaccination coverage for the total population was 99.0%. Incomplete vaccination coverage is not a valid explanation for the Quebec City measles outbreak.” https://www.ncbi.nlm.nih.gov/m/pubmed/1884314/

103. We conclude 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. https://www.ncbi.nlm.nih.gov/m/pubmed/3821823/

104. Xenotropic murine leukemia virus-related virus (XMRV) is a recently discovered human retrovirus that has been found in both chronic fatigue syndrome & prostate cancer patients. There is a potential safety concern regarding XMRV in cell substrates used in vaccines...http://www.fda.gov/.../biologicsresearchareas/ucm127327.htm

105. Vaccines spread disease. Pertussis lives in the throats of the recently vaccinated, making them asymptomatic carriers who can (and do) spread the disease: http://web.archive.org/…/N…/PressAnnouncements/ucm376937.htm

106. Transmission of Vaccine Derived Polio Virus https://www.ncbi.nlm.nih.gov/m/pubmed/19090774/

107. Polio shedding: https://www.ncbi.nlm.nih.gov/m/pubmed/8228342/

108. Transmission of vaccine derived mumps: https://www.ncbi.nlm.nih.gov/m/pubmed/24772647/

109. More vaccine mumps transmission: https://www.ncbi.nlm.nih.gov/m/pubmed/16266774/

110. Transmission of vaccine derived varicella: https://www.ncbi.nlm.nih.gov/m/pubmed/9255208/

111. More transmission of vaccine varicella: https://www.ncbi.nlm.nih.gov/m/pubmed/16769402/

112. Varicella shedding: http://m.jid.oxfordjournals.org/content/203/11/1542.full

113. More rotavirus shedding: https://www.ncbi.nlm.nih.gov/m/pubmed/18922486/

114. Vaccine derived measles shedding: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC228449/

115. Measles transmission from a twice vaccinated individual: http://m.cid.oxfordjournals.org/…/ear…/2014/02/27/cid.ciu105

116. More measles transmission: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1646939/

117. Shedding Measles: https://www.ncbi.nlm.nih.gov/m/pubmed/15804301/

118. Flu shot sheds: https://www.ncbi.nlm.nih.gov/m/pubmed/18662737/

119. More flu shed: https://www.ncbi.nlm.nih.gov/m/pubmed/21513761/?i=3

120. Fewer than 1% of polio results in paralysis https://www.cdc.gov/vaccines/pubs/pinkbook/polio.html

121. The first polio vaccine was worked on by Dr. Jonas Salk and human experiments using this vaccine were conducted purposely on orphans in government/church run institutions because they were vulnerable and didn’t require any parental consent signatures, as they had no parents. The vaccine was “declared safe” by “medicine” (as they always are even though that vaccine was killing and paralyzing monkeys in test trials) and that vaccine gave 40,000 orphans polio, permanently paralyzed hundreds and killed at least 10 children. All injuries and deaths under reported of course by the same authorities who orchestrated the atrocity. This was called The Cutter Incident. A focused attack on defenseless children, by people charged with their care. A poisoning of innocent children and then the excuses and apologies, regarding how it won’t happen again. Is this pattern still occurring today? The answer is obvious.

http://1.usa.gov/1mEozNJ

122. "Behavioral testing showed motor deficits in the aluminum treatment group that expressed as a progressive decrease in strength measured by the wire-mesh hang test (final deficit at 24 wk; about 50%). Significant cognitive deficits in water-maze learning were observed in the combined aluminum and squalene group (4.3 errors per trial) compared with the controls (0.2 errors per trial) after 20 wk. Apoptotic neurons were identified in aluminum-injected animals that showed significantly increased activated caspase-3 labeling in lumbar spinal cord (255%) and primary motor cortex (192%) compared with the controls. Aluminum-treated groups also showed significant motor neuron loss (35%) and increased numbers of astrocytes (350%) in the lumbar spinal cord."

https://www.ncbi.nlm.nih.gov/m/pubmed/17114826/

123. The demonstration of neuropathological outcomes and behavioural deficits in aluminum hydroxide injected mice may provide some insight into the causes of not only GWS–ALS, but may open avenues of investigation into other neurological diseases."

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2819810/

124. Aluminum hydroxide injections lead to motor deficits and motor neuron

FDA on aluminum https://www.accessdata.fda.gov/…/cfdocs/cfcfr/CFRSearch.cfm…

125. A recent study says this... "All currently available evidence suggests that DTP vaccine may kill more children from other causes than it saves from diphtheria, tetanus or pertussis."

No apparent conflict of interest, hasn't been debunked/discredited and was even funded in part by a large pharmaceutical company (Novo Nordisk).

Link to the study: https://www.ncbi.nlm.nih.gov/…/arti…/PMC5360569/pdf/main.pdf

126. Also: DTP SIDS https://www.ncbi.nlm.nih.gov/pubmed/6835859/

127. DTaP Pregnancy Adverse Effects https://www.ncbi.nlm.nih.gov/pubmed/22727350/

128. Long Term Studies

The agency that's supposed to extensively study its product, observe the vaccinated population, for both short and long term impact on children. -The CDC - admits the total opposite. (also they’re a major vax patent-holder (over 20, I believe), and a subsidiary of the pharmaceutical industry.) They admit that long term studies on vaccines aren't done because it's not "practical" and would be "unethical" to stop giving them to prove their safety.

In its own "Parents' Guide to Faux Immunity," --- “Q: How do we know vaccines aren’t causing long-term health problems? A: Observing vaccinated children for many years to look for long-term health conditions would not be practical, and withholding an effective vaccine from children while long-term studies are being done wouldn’t be ethical.”

https://www.cdc.gov/…/parents-guide/parents-guide-part4.html

"Effective?" How? Slam dunk that every vaccinated adult and child is the test subject, and for any health problems arising – or death - after the vaxxes, to never be linked to the vaxxes.

Because THAT'S practical....according to the CDC.

129. The bloodstream is where heavy metals bind to some amino acids and transferrin receptors. In fact, infants’ brains let in more of these (not due to blood brain barrier - that still works, but due to needing them more for brain development) than adults. So if there are toxic metals in there, then they’ll inadvertently get more of those too. Because of vulnerability of the developing brain to heavy metals this transport may contribute to fetal or newborn neurotoxicity, whereas adults can deal with it to a greater extent. Barrier Mechanisms in the Developing Brain: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314990/

130. Barrier Mechanisms in the Developing Brain The adult brain functions within a well-controlled stable environment, the properties of which are determined by cellular exchange mechanisms superimposed on the diffusion restraint provided by tight junctions at interfaces between blood, brain and cerebrospinal ... ncbi.nlm.nih.gov

131. Toxicity Safety- Do you know what the toxicity safety standard is for vaccines? Whether or not mice gain weight. Not whether they develop autoimmune disease, not seizures, not eczema, food allergies, not whether the mice go into a deep sleep that takes hours to wake up from and grow enlarged heads. Just whether or not the mice gain weight. Does that sound like a safety test to you? https://www.ncbi.nlm.nih.gov/m/pubmed/7811458/

132. It was the high incidence of diabetes from the HiB vaccines which banned the shot forever from Finland. We still give 4 doses to our kids. And what is the incidence of childhood diabetes in the US in the last 15 years? http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1116914/ �http://www.ncbi.nlm.nih.gov/…/www.ncbi.nlm.…/pubmed/25598306

133. An Australian National Health and Medical Council information sheet on Hib vaccines advises that Hib meningitis can cause brain damage with later learning difficulties and behavioural disorders (www.health.gov.au). Fungal meningitis is not contagious�Parasitic meningitis is not�Non-infectious meningitis is not Viral meningitis.. The enteroviruses that cause viral meningitis can spread through direct contact with saliva, nasal mucus, or feces. They easily spread through coughing and sneezing but you are unlikely to develop meningitis as a complication. Bacterial meningitis is contagious but is less contagious than the germs that spread cold and flu. Meningococcal bacteria can’t survive outside the body for long, so you are unlikely to get it from being near someone who has it.

134.-136. Kawasaki disease is an autoimmune disorder following antigenic stimulation in a genetically susceptible child which causes insulin deficiency and failure of the cellular uptake of vitamin C, tissue scurvy, and can be mistaken for child abuse. Vaccines are a proven cause of hyperglycemia in children and may be a cause of Kawasaki disease. - this is what my son had. �https://www.ncbi.nlm.nih.gov/m/pubmed/26634312/� https://web.archive.org/…/co…/kawasaki_disease_rotavirus.htm

137. http://www.fda.gov/…/Vaccines/ApprovedProducts/UCM133539.pdf

138. Gardisil adjuvant http://www.nvic.org/…/Preventing-Gardasil-Vaccine-Injuries-…

139. Published in Current Medicinal Chemistry, 2011: Aluminum Vaccine Adjuvants: Are they Safe? source + full text: http://www.meerwetenoverfreek.nl/…/Tomljenovic_Shaw-CMC-pub… Published in the Journal of Exposure Science and Environmental Epidemiology, 2010: Infants' exposure to aluminum from vaccines and breast milk during the first 6 months. source + full text: http://www.nature.com/…/journal/v20/n7/full/jes200964a.html�

140. Published in Expert Review of Vaccines, 2007: Neurological adverse events of immunization: experience with an aluminum adjuvanted meningococcal B outer membrane vesicle vaccine. source: http://www.ncbi.nlm.nih.gov/pubmed/17931164

full text: http://www.medscape.com/viewarticle/565691_3

141. Do aluminum vaccine adjuvants contribute to the rising prevalence of autism? http://www.ncbi.nlm.nih.gov/pubmed/22099159

Our results show that: (i) children from countries with the highest ASD prevalence appear to have the highest exposure to Al from vaccines; (ii) the increase in exposure to Al adjuvants significantly correlates with the increase in ASD prevalence in the United States observed over the last two decades;

and (iii) a significant correlation exists between the amounts of Al administered to preschool children and the current prevalence of ASD in seven Western countries, particularly at 3-4 months of age.

142. Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2819810/…

...A second series of experiments was conducted on mice injected with six doses of aluminum hydroxide. Behavioural analyses in these mice revealed significant impairments in a number of motor functions as well as diminished spatial memory capacity.

143. Aluminum Vaccine Adjuvants: Are they Safe? http://www.ncbi.nlm.nih.gov/pubmed/21568886

Experimental research, 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. click for entire study

144. Aluminum-Induced Entropy in Biological Systems: Implications for Neurological Disease http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202242/

1.2. The Toxic Effects of Aluminum as a Vaccine Adjuvant

Al salts (hydroxide and phosphate) are the most commonly used vaccine adjuvants and, until recently, the only adjuvants licensed for use in the USA [79–89]. In the absence of Al, according to their manufacturers, antigenic components of most vaccines (with the exception of live attenuated vaccines) fail to elicit the desired level of immune response [66, 80]. Although Al is neurotoxic, it is claimed by proponents that the concentrations at which Al is used in the vaccines do not represent a health hazard [19]. For that reason, vaccine trials often treat an Al adjuvant-containing injection as a harmless “placebo” (a comparison benchmark or control treatment) or they use another Al-containing vaccine to treat a “control group,” despite evidence that Al in vaccine-relevant exposures is universally toxic to humans and animals [9, 90, 91]. Its use in a supposed “placebo” or in any “control” treatment in vaccine trials is indefensible [95]. It is precisely analogous to comparing fire A against fire B, to make the argument that since A is no hotter than B, A is therefore not a fire.

During the last decade, studies on animal models and humans have shown that Al adjuvants by themselves cause autoimmune and inflammatory conditions [19, 79–81, 90, 95–103]. The animal models show that subcutaneous injections of Al hydroxide induced apoptotic neuronal death and decreased motor function in mice [2, 37–39] and sheep [43]. In newborn mice they were associated with weight increases, behavioral changes, and increased anxiety [2]. All these findings plausibly implicate Al adjuvants in pediatric vaccines as causal factors contributing to increased rates of autism spectrum disorders in countries where multiple doses are almost universally administered [9]. Also, as shown by Goldman and Miller in studies published in 2011 and 2012, strong correlations between infant mortality rates and the number of doses of vaccines administered also suggest deleterious impact of multiple exposures to their components [104, 105]. Follow-up experiments focusing on Al adjuvants in mice by Khan et al. [106] have shown that the adjuvants do not stay localized in the muscle tissue upon intramuscular injection. The particles can travel to the spleen and brain where they can be detected up to a year after the injection. Such findings refute the notion that adjuvant nanoparticles remain localized and act through a “depot effect.” On the contrary, the Al from vaccine adjuvants does cross the blood-brain and blood-cerebrospinal fluid barriers and incites deleterious immunoinflammatory responses in neural tissues [1–3, 9]. Tracking experiments in mice reveal that some Al hydroxide nanoparticles escape the injected muscle inside immune system cells such as macrophages, which travel to regional draining lymph nodes, where it can exit to the bloodstream gaining access to all organ systems, including the brain. As Khan et al. [106] have warned, repeated doses of Al hydroxide are “insidiously unsafe,” especially in closely spaced challenges presented to an infant or a person with damaged or immature blood brain or cerebrospinal fluid barriers [2]. Given macrophages acting as highly mobile “Trojan horses” [107], the Khan et al. warning suggests that cumulative Al from repeated doses in vaccines can produce the cognitive deficits associated with long-term encephalopathies and degenerative dementias in humans [40, 99]. The latest research by Luján et al. [43] described a severe neurodegenerative syndrome in commercial sheep linked to the repetitive inoculation of Al-containing vaccines. In particular, the “sheep adjuvant syndrome” mimics in many aspects human neurological diseases linked to Al adjuvants. Moreover, the outcomes in sheep were first identified following a mass-vaccination campaign against blue tongue and have now been successfully reproduced under experimental conditions following administration of Al-containing vaccines. Notably, the adverse chronic phase of this syndrome affects 50–70% of the treated flocks and up to 100% of the animals within a given flock. The disorder is made worse by cold weather conditions, suggesting synergy with other stress producing factors. The disorder is characterized by severe neurobehavioral outcomes—restlessness, compulsive wool biting, generalized weakness, muscle tremors, loss of response to stimuli, ataxia, tetraplegia, stupor, inflammatory lesions in the brain and the presence of Al in the CNS tissues, coma, and death [43]. These findings confirm and extend those of Khan et al. [106] who demonstrated the ability of Al adjuvants to cross the BBB, and they show that Al in the brain can trigger severe long-term neurological damage. The findings by Luján et al. [43] and Khan et al. [106] also show how and why reported adverse reactions following vaccinations are most commonly neurological and neuropsychiatric [6,7].

Keyword:legit

Info Complied by: Amber Brown