Vaccine News – Study – Blood Levels of Mercury Are Related to Diagnosis of Autism: A Reanalysis of an Important Data Set & VAXXED TV – Vaccines gave my son autism

A study published in the Journal of Child Neurology examined the question of what is leading to the apparent increase in autism. They expressed that if there is any link between autism and mercury, it is crucial that the first reports of the question are not falsely stating that no link occurs. Researchers determined that a significant relation does exist between the blood levels of mercury and the diagnosis of an autism spectrum disorder.

Journal of Child Neurology
First Published November 1, 2007

Study – Blood Levels of Mercury Are Related to Diagnosis of Autism: A Reanalysis of an Important Data Set

M. Catherine DeSoto, PhD, Robert T. Hitlan, PhD
Department of Psychology, University of Northern Iowa, Cedar Falls, Iowa,

Abstract
The question of what is leading to the apparent increase in autism is of great importance. Like the link between aspirin and heart attack, even a small effect can have major health implications. If there is any link between autism and mercury, it is absolutely crucial that the first reports of the question are not falsely stating that no link occurs. We have reanalyzed the data set originally reported by Ip et al. in 2004 and have found that the original p value was in error and that a significant relation does exist between the blood levels of mercury and diagnosis of an autism spectrum disorder. Moreover, the hair sample analysis results offer some support for the idea that persons with autism may be less efficient and more variable at eliminating mercury from the blood.

A study published in the Journal of Child Neurology noted that autistic spectrum disorders can be associated with mitochondrial dysfunction. Researchers determined that children who have mitochondrial-related dysfunctional cellular energy metabolism might be more prone to undergo autistic regression between 18 and 30 months of age if they also have infections or immunizations at the same time.

Journal of Child Neurology
First Published February 1, 2006

Study – Developmental Regression and Mitochondrial Dysfunction in a Child With Autism
1 – Jon S. Poling, MD, PhD, 2 – Richard E. Frye, MD, PhD, 3 – John Shoffner, MD, 4 – Andrew W. Zimmerman, MD
1 – Department of Neurology and Neurosurgery Johns Hopkins Hospital Baltimore, MD
2 – Department of Neurology Boston Children’s Hospital Boston, MA
3 – Horizon Molecular Medicine Georgia State University Atlanta, GA
4 – Department of Neurology and Neurosurgery Johns Hopkins Hospital Kennedy Krieger Institute Baltimore, MD

Abstract
Autistic spectrum disorders can be associated with mitochondrial dysfunction. We present a singleton case of developmental regression and oxidative phosphorylation disorder in a 19-month-old girl. Subtle abnormalities in the serum creatine kinase level, aspartate aminotransferase, and serum bicarbonate led us to perform a muscle biopsy, which showed type I myofiber atrophy, increased lipid content, and reduced cytochrome c oxidase activity. There were marked reductions in enzymatic activities for complex I and III. Complex IV (cytochrome c oxidase) activity was near the 5% confidence level. To determine the frequency of routine laboratory abnormalities in similar patients, we performed a retrospective study including 159 patients with autism (Diagnostic and Statistical Manual of Mental Disorders-IV and Childhood Autism Rating Scale) not previously diagnosed with metabolic disorders and 94 age-matched controls with other neurologic disorders. Aspartate aminotransferase was elevated in 38% of patients with autism compared with 15% of controls (P < .0001). The serum creatine kinase level also was abnormally elevated in 22 (47%) of 47 patients with autism. These data suggest that further metabolic evaluation is indicated in autistic patients and that defects of oxidative phosphorylation might be prevalent.

A study conducted by Massachusetts General Hospital at the Centre for Morphometric Analysis by the department of Paediatric Neurology illustrates how autistic brains have a growth spurt shortly after birth and then slow in growth a few short years later. Researchers have determined that neuroinflammation appears to be present in autistic brain tissue from childhood through adulthood. The study excerpt reads:
“Oxidative stress, brain inflammation and microgliosis have been much documented in association with toxic exposures including various heavy metals. The awareness that the brain as well as medical conditions of children with autism may be conditioned by chronic biomedical abnormalities such as inflammation opens the possibility that meaningful biomedical interventions may be possible well past the window of maximal neuroplasticity in early childhood because the basis for assuming that all deficits can be attributed to fixed early developmental alterations in net”

US National Library of Medicine
National Institutes of Health – 2005

Study – Large brains in autism: the challenge of pervasive abnormality

Herbert MR.
Author information
Pediatric Neurology, Center for Morphometric Analysis, Massachusetts General Hospital, Charleston, MA 02129, USA. mherbert1@partners.org

Abstract
The most replicated finding in autism neuroanatomy-a tendency to unusually large brains-has seemed paradoxical in relation to the specificity of the abnormalities in three behavioral domains that define autism. We now know a range of things about this phenomenon, including that brains in autism have a growth spurt shortly after birth and then slow in growth a few short years afterward, that only younger but not older brains are larger in autism than in controls, that white matter contributes disproportionately to this volume increase and in a nonuniform pattern suggesting postnatal pathology, that functional connectivity among regions of autistic brains is diminished, and that neuroinflammation (including microgliosis and astrogliosis) appears to be present in autistic brain tissue from childhood through adulthood. Alongside these pervasive brain tissue and functional abnormalities, there have arisen theories of pervasive or widespread neural information processing or signal coordination abnormalities (such as weak central coherence, impaired complex processing, and underconnectivity), which are argued to underlie the specific observable behavioral features of autism. This convergence of findings and models suggests that a systems- and chronic disease-based reformulation of function and pathophysiology in autism needs to be considered, and it opens the possibility for new treatment targets.

VAXXED TV – Unvaccinated family with no cancer

Vaccines ruined my daughters life

No more vaccines for my children

My son had food allergies and autism from vaccines

Vaccines gave my son autism

Unvaccinated and healthy #vaxxed #Praybig

Vaccines have my son autism and epilepsy

Vaccines have completely destroyed my son

I’m a former pro vaccine nurse

Vaccines destroyed my family

****************************************************

How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:

Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.

 

Advertisements

Vaccine News – VAXXED TV – What If I Harmed My Children

Study – Comparison of Blood and Brain Mercury Levels in Infant Monkeys Exposed to Methylmercury or Vaccines Containing Thimerosal

Environmental Health – Apr 2005

Thomas M. Burbacher, Danny D. Shen, Noelle Liberato,
Kimberly S. Grant, Elsa Cernichiari, and Thomas Clarkson

Abstract
Thimerosal is a preservative that has been used in manufacturing vaccines since the 1930s. Reports have indicated that infants can receive ethylmercury (in the form of thimerosal) at or above the Environmental Protection Agency (EPA) guidelines for methylmercury (MeHg) exposure, depending on the exact vaccinations, schedule, and size of the infant. This study compared the systemic disposition and brain distribution of total and inorganic mercury in infant monkeys following thimerosal exposure with infants exposed to MeHg. Monkeys were exposed to MeHg (via oral gavage) or vaccines containing thimerosal (via i.m. injection) at birth and 1, 2, and 3 weeks of age. Total blood mercury (Hg) levels were determined 2, 4 and 7 days after each exposure. Total and inorganic brain Hg levels were assessed 2, 4, 7 or 28 days after the last exposure. The initial and terminal half-life of Hg in blood following thimerosal exposure was 2.1 and 8.6 days, which are significantly shorter than the elimination half-life of Hg following MeHg exposure at 21.5 days. Brain concentrations of total Hg were significantly lower by ~3-fold for the thimerosal-exposed infants when compared to the MeHg infants, while the average brain-to-blood concentration ratio was slightly higher for the thimerosal-exposed infants (3.5±1.0 vs. 2.5±0.6). A higher percentage of the total Hg in the brain was in the form of inorganic mercury for the thimerosal-exposed infants (34% vs 7%). The current study indicates that MeHg is not a suitable reference for risk assessment from exposure to thimerosal derived Hg. Knowledge of the toxicokinetics and developmental toxicity of thimerosal is needed to afford a meaningful assessment of the developmental effects of thimerosal-containing vaccines.

Study – Evolution of multiple sclerosis in France since the beginning of hepatitis B vaccination

US National Library of Medicine
National Institutes of Health – 14 Nov 2014

Dominique Le Houézeccorresponding author
REVAHB (“Réseau Vaccin Hépatite B” in French), 32 rue du Clos Herbert, 14000 Caen, France

Abstract
Since the implementation of the mass vaccination campaign against hepatitis B in France, the appearance of multiple sclerosis, sometimes occurring in the aftermath of vaccinations, led to the publication of epidemiological international studies. This was also justified by the sharp increase in the annual incidence of multiple sclerosis reported to the French health insurance in the mid-1990s. Almost 20 years later, a retrospective reflection can be sketched from these official data and also from the national pharmacovigilance agency. Statistical data from these latter sources seem to show a significant correlation between the number of hepatitis B vaccinations performed and the declaration to the pharmacovigilance of multiple sclerosis occurring between 1 and 2 years later. The application of the Hill’s criteria to these data indicates that the correlation between hepatitis B vaccine and multiple sclerosis may be causal.

Temporal Association of Certain Neuropsychiatric Disorders Following Vaccination of Children and Adolescents: A Pilot Case–Control Study

Douglas L. Leslie1*, imageRobert A. Kobre2, imageBrian J. Richmand2, imageSelin Aktan Guloksuz2 and imageJames F. Leckman2*

1 Department of Public Health Sciences, Pennsylvania State University College of Medicine, Hershey, PA, USA
2 Yale Child Study Center, Yale University School of Medicine, New Haven, CT, USA

Background: Although the association of the measles, mumps, and rubella vaccine with autism spectrum disorder has been convincingly disproven, the onset of certain brain-related autoimmune and inflammatory disorders has been found to be temporally associated with the antecedent administration of various vaccines. This study examines whether antecedent vaccinations are associated with increased incidence of obsessive–compulsive disorder (OCD), anorexia nervosa (AN), anxiety disorder, chronic tic disorder, attention deficit hyperactivity disorder, major depressive disorder, and bipolar disorder in a national sample of privately insured children.

Methods: Using claims data, we compared the prior year’s occurrence of vaccinations in children and adolescents aged 6–15 years with the above neuropsychiatric disorders that were newly diagnosed between January 2002 and December 2007, as well as two control conditions, broken bones and open wounds. Subjects were matched with controls according to age, gender, geographical area, and seasonality. Conditional logistic regression models were used to determine the association of prior vaccinations with each condition.

Results: Subjects with newly diagnosed AN were more likely than controls to have had any vaccination in the previous 3 months [hazard ratio (HR) 1.80, 95% confidence interval 1.21–2.68]. Influenza vaccinations during the prior 3, 6, and 12 months were also associated with incident diagnoses of AN, OCD, and an anxiety disorder. Several other associations were also significant with HRs greater than 1.40 (hepatitis A with OCD and AN; hepatitis B with AN; and meningitis with AN and chronic tic disorder).

Conclusion: This pilot epidemiologic analysis implies that the onset of some neuropsychiatric disorders may be temporally related to prior vaccinations in a subset of individuals. These findings warrant further investigation, but do not prove a causal role of antecedent infections or vaccinations in the pathoetiology of these conditions. Given the modest magnitude of these findings in contrast to the clear public health benefits of the timely administration of vaccines in preventing mortality and morbidity in childhood infectious diseases, we encourage families to maintain vaccination schedules according to CDC guidelines.

VAXXED TV – I can’t believe they are doing this!
Patricia Gua tells of her injuries from receiving the HEP-B vaccination.
Interview recorded on May 5th, 2017 in The United Kingdom

What If I Harmed My Children
Kelly Johnson, author of “What If?: I Harmed My Children” gives detailed accounts of her experiences with her kids which inspired her to write the book. You can find a copy of it for purchase or download here: http://a.co/6Fy23cJ
Interview recorded on May 5th, 2017 in The United Kingdom

I had every reaction documented
Liola shares about the details of her children’s reactions to vaccinations and the challenges they faced.
Interview recorded on May 5th, 2017 in The United Kingdom

It’s sad we have to learn the hard way
A mother shares her story about her children’s reactions to the vaccines.
Interview recorded on May 5th, 2017 in The United Kingdom

Know Your Body

Drunk on Toxins

Mark Blaxill

A Tribute To Polly Tommey

Dr Suzanne- more herd immunity

Vaccinated versus unvaccinated

****************************************************

How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:

Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.

Vaccine News – Study – The Blood-Brain Barrier Bottleneck in Brain Drug Development

Study – Systematic review and meta-analysis links autism and toxic metals and highlights the impact of country development status: Higher blood and erythrocyte levels for mercury and lead, and higher hair antimony, cadmium, lead, and mercury.

US National Library of Medicine
National Institutes of Health – 3 Oct 2017

Saghazadeh A – 1, Rezaei N – 2.
Author information
1 Research Center for Immunodeficiencies, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran; MetaCognition Interest Group (MCIG), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
2 Research Center for Immunodeficiencies, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran; Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran; Systematic Review and Meta-analysis Expert Group (SRMEG), Universal Scientific Education and Research Network (USERN), Boston, MA, USA. Electronic address: Rezaei_nima@tums.ac.ir.

Abstract
BACKGROUND:
Autism spectrum disorder (ASD) is a heterogeneous neurodevelopmental disorder that affects cognitive and higher cognitive functions. Increasing prevalence of ASD and high rates of related comorbidities has caused serious health loss and placed an onerous burden on the supporting families, caregivers, and health care services. Heavy metals are among environmental factors that may contribute to ASD. However, due to inconsistencies across studies, it is still hard to explain the association between ASD and toxic metals. Therefore the objective of this study was to investigate the difference in heavy metal measures between patients with ASD and control subjects.
METHODS:
We included observational studies that measured levels of toxic metals (antimony, arsenic, cadmium, lead, manganese, mercury, nickel, silver, and thallium) in different specimens (whole blood, plasma, serum, red cells, hair and urine) for patients with ASD and for controls. The main electronic medical database (PubMed and Scopus) were searched from inception through October 2016.
RESULTS:
52 studies were eligible to be included in the present systematic review, of which 48 studies were included in the meta-analyses. The hair concentrations of antimony (standardized mean difference (SMD)=0.24; 95% confidence interval (CI): 0.03 to 0.45) and lead (SMD=0.60; 95% confidence interval (CI): 0.17 to 1.03) in ASD patients were significantly higher than those of control subjects. ASD patients had higher erythrocyte levels of lead (SMD=1.55, CI: 0.2 to 2.89) and mercury (SMD=1.56, CI: 0.42 to 2.70). There were significantly higher blood lead levels in ASD patients (SMD=0.43, CI: 0.02 to 0.85). Sensitivity analyses showed that ASD patients in developed but not in developing countries have lower hair concentrations of cadmium (SMD=-0.29, CI: -0.46 to -0.12). Also, such analyses indicated that ASD patients in developing but not in developed lands have higher hair concentrations of lead (SMD=1.58, CI: 0.80 to 2.36) and mercury (SMD=0.77, CI: 0.31 to 1.23). These findings were confirmed by meta-regression analyses indicating that development status of countries significantly influences the overall effect size of mean difference for hair arsenic, cadmium, lead, and mercury between patients with ASD and controls.
CONCLUSION:
The findings help highlighting the role of toxic metals as environmental factors in the etiology of ASD, especially in developing lands. While there are environmental factors other than toxic metals that greatly contribute to the etiology of ASD in developed lands. It would be, thus, expected that classification of ASD includes etiological entities of ASD on the basis of implication of industrial pollutants (developed vs. developing ASD).

Study – Autism: A form of lead and mercury toxicity

Environmental Toxicology and Pharmacology
Volume 38, Issue 3, November 2014, Pages 1016–1024

Highlights
•Autism is a developmental disability characterized by severe, pervasive deficits in social interaction and communications.
•Lead and mercury two of the most common heavy metals in the environment.
•Lead and mercury can lead to autistic disorders.
•Many risk factors contribute to the high level of heavy metals in autistic children.
•Defect in the metabolism of the heavy metals in autistic children also contribute to the high level of these heavy metals in their body.
•Chelating agents can be used in the treatment of the autistic disorders.

Abstract
Aim
Autism is a developmental disability characterized by severe deficits in social interaction and communication. The definite cause of autism is still unknown. The aim of this study is to find out the relation between exposure to Lead and/or mercury as heavy metals and autistic symptoms, dealing with the heavy metals with chelating agents can improve the autististic symptoms.

Method
Blood and hair samples were obtained from 45 children from Upper Egypt with autism between the ages of 2 and 10 years and 45 children served as controls in the same age range, after taken an informed consent and fill a questionnaire to assess the risk factors. The samples were analyzed blindly for lead and mercury by using atomic absorption and ICP-MS. Data from the two groups were compared, then follow up of the autistic children after treatment with chelating agents were done.

Results
The results obtained showed significant difference among the two groups, there was high level of mercury and lead among those kids with autism. Significant decline in the blood level of lead and mercury with the use of DMSA as a chelating agent. In addition, there was decline in the autistic symptoms with the decrease in the lead and mercury level in blood.

Conclusion
Lead and mercury considered as one of the main causes of autism. Environmental exposure as well as defect in heavy metal metabolism is responsible for the high level of heavy metals. Detoxification by chelating agents had great role in improvement of those kids.

Study – The Blood-Brain Barrier: Bottleneck in Brain Drug Development

US National Library of Medicine
National Institutes of Health – Jan 2005

William M. Pardridge
Department of Medicine, UCLA, Los Angeles, California 90024
Address correspondence and reprint requests to William M. Pardridge, M.D., UCLA Warren Hall, 13-164, 900 Veteran Avenue, Los Angeles,

ABSTRACT
Summary: The blood-brain barrier (BBB) is formed by the brain capillary endothelium and excludes from the brain ∼100% of large-molecule neurotherapeutics and more than 98% of all small-molecule drugs. Despite the importance of the BBB to the neurotherapeutics mission, the BBB receives insufficient attention in either academic neuroscience or industry programs. The combination of so little effort in developing solutions to the BBB problem, and the minimal BBB transport of the majority of all potential CNS drugs, leads predictably to the present situation in neurotherapeutics, which is that there are few effective treatments for the majority of CNS disorders. This situation can be reversed by an accelerated effort to develop a knowledge base in the fundamental transport properties of the BBB, and the molecular and cellular biology of the brain capillary endothelium. This provides the platform for CNS drug delivery programs, which should be developed in parallel with traditional CNS drug discovery efforts in the molecular neurosciences.

VAXXED TV – Nick Johansen #vaxxed #PrayBig

Dr. Judy Mikovits, PhD Research Scientist at #TxMFA #TxMFA2017
Dr. Judy Mikovits, PhD research scientist, dives deep into the crude science of vaccination

Austin Bennett #vaxxed #PrayBig

Dawn Richardson

David Oldham

Barbara Loe Fisher #vaxxed #truth #science #praybig

Q&A vaccine syndrome

Global Vaccine Initiative Houston Protest #TxMFA #TxMFA2017
Jonathan Tommey and The Vaxxed Team hit the ground running at the Texas Medical Freedom Alliance world symposium in Housant, Texas.
They discusses vaccine safety concerns with our #TexasPeeps protesting on the ground and also interview medical doctor, Jim Meehan, M.D. with regard to his passion for exposing the deception endemic to the present vaccine paradigm.

Glaxo’s Vaccine Trials survivor speaks out
David tells his story and presents documentation of his history going through the Glaxo’s trials. His mother was told he had passed as an infant here they kept him as an orphan until 4 years old.
Interview recorded on May 5th, 2017 in The United Kingdom

****************************************************

How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:

Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.

Vaccine News – Associations of prenatal and early childhood mercury exposure with autistic behaviors at 5 years of age: The Mothers and Children’s Environmental Health (MOCEH) study

Science of The Total Environment – 2017
Highlights
•We explored the associations between blood mercury levels and autistic behaviors.
•This study involved an ongoing multi-center prospective birth cohort.
•Blood mercury levels were repeatedly measured from early pregnancy to 3 years.
•Autistic behaviors were assessed at 5 years with the Social Responsiveness Scale.
•Prenatal and early childhood mercury levels were associated with autistic behaviors.
Abstract
Background
Although mercury is an established neurotoxin, only few longitudinal studies have investigated the association between prenatal and early childhood mercury exposure and autistic behaviors.
Methods
We conducted a longitudinal cohort study using an ongoing prospective birth cohort initiated in 2006, wherein blood mercury levels were measured at early and late pregnancy; in cord blood; and at 2 and 3 years of age. We analyzed 458 mother-child pairs. Autistic behaviors were assessed using the Social Responsiveness Scale (SRS) at 5 years of age. Both continuous SRS T-scores and T-scores dichotomized by a score of ≥ 60 or < 60 were used as outcomes.
Results
The geometric mean of mercury concentrations in cord blood was 5.52 μg/L. In adjusted models, a doubling of blood mercury levels at late pregnancy (β = 1.84, 95% confidence interval [CI]: 0.39, 3.29), in cord blood (β = 2.24, 95% CI: 0.22, 4.27), and at 2 years (β = 2.12, 95% CI: 0.54, 3.70) and 3 years (β = 2.80, 95% CI: 0.89, 4.72) of age was positively associated with the SRS T-scores. When the SRS T-scores were dichotomized, we observed positive associations with mercury levels at late pregnancy (relative risk [RR] = 1.31, 95% CI: 1.08, 1.60) and in cord blood (RR = 1.28, 95% CI: 1.01, 1.63).
Conclusion
We found that blood mercury levels at late pregnancy and early childhood were associated with more autistic behaviors in children at 5 years of age. Further study on the long-term effects of mercury exposure is recommended.
Molecular Neurobiology – 22 July 2017
Abstract
Exposure to organic forms of mercury has the theoretical capacity to generate a range of immune abnormalities coupled with chronic nitro-oxidative stress seen in children with autism spectrum disorder (ASD). The paper discusses possible mechanisms explaining the neurotoxic effects of mercury and possible associations between mercury exposure and ASD subtypes. Environmental mercury is neurotoxic at doses well below the current reference levels considered to be safe, with evidence of neurotoxicity in children exposed to environmental sources including fish consumption and ethylmercury-containing vaccines. Possible neurotoxic mechanisms of mercury include direct effects on sulfhydryl groups, pericytes and cerebral endothelial cells, accumulation within astrocytes, microglial activation, induction of chronic oxidative stress, activation of immune-inflammatory pathways and impairment of mitochondrial functioning. (Epi-)genetic factors which may increase susceptibility to the toxic effects of mercury in ASD include the following: a greater propensity of males to the long-term neurotoxic effects of postnatal exposure and genetic polymorphisms in glutathione transferases and other glutathione-related genes and in selenoproteins. Furthermore, immune and inflammatory responses to immunisations with mercury-containing adjuvants are strongly influenced by polymorphisms in the human leukocyte antigen (HLA) region and by genes encoding effector proteins such as cytokines and pattern recognition receptors. Some epidemiological studies investigating a possible relationship between high environmental exposure to methylmercury and impaired neurodevelopment have reported a positive dose-dependent effect. Retrospective studies, on the other hand, reported no relationship between a range of ethylmercury-containing vaccines and chronic neuropathology or ASD. On the basis of these results, we would argue that more clinically relevant research is required to examine whether environmental mercury is associated with ASD or subtypes. Specific recommendations for future research are discussed.
PubMed.gov – 8 May 2017
Abstract
Environmental factors have been implicated in the etiology of autism spectrum disorder (ASD); however, the role of heavy metals has not been fully defined. This study investigated whether blood levels of mercury, arsenic, cadmium, and lead of children with ASD significantly differ from those of age- and sex-matched controls. One hundred eighty unrelated children with ASD and 184 healthy controls were recruited. Data showed that the children with ASD had significantly (p < 0.001) higher levels of mercury and arsenic and a lower level of cadmium. The levels of lead did not differ significantly between the groups. The results of this study are consistent with numerous previous studies, supporting an important role for heavy metal exposure, particularly mercury, in the etiology of ASD. It is desirable to continue future research into the relationship between ASD and heavy metal exposure

Vaccine News – It is estimated that Vioxx killed more U.S. citizens than the Vietnam War

Autism Parents: It’s going to be all right.
WAY TOO MANY families with kids on the Autism Spectrum are having WAY TOO MANY difficulties. Please share this link with EVERY Autism family that you care about: https://thriveinchaos.net/mini-workshop-welcome/
It’s a free Mini-Workshop that shares what other families are doing to “THRIVE IN CHAOS.” Together, let’s make the Autism world a less stressed, happier place.

A family’s life in ruins .. after the flu vaccine left their baby girl disabled.
Dixie Marshall’s Exclusive report.

Aborted Human DNA & Fetal Calf Blood Are Ingredients In Children’s Vaccines
By Tami Canal On March 30, 2017
Aside from the looming threat of the loss of medical freedom in regards to vaccination, what should truly frighten parents is the fact that there has never been a single safety study conducted on the inter-relationship between multiple vaccines, nor has there ever been a single safety study as far as the combination of ingredients in the vaccines themselves.
The medical industry, pediatricians, and unsuspecting parents are blindly trusting the CDC’s assertions of safety. And while we are discussing frightening matters, it should also be noted that neither the CDC nor the FDA can prove the safety of the current vaccine schedule. For further information, check out this link.
Mandatory vaccination laws are already a reality in states like California and Mississippi, and it has never been more dire for parents to understand the shocking ingredients in those vaccine vials. As advocates for our children, it is our job to be fully educated on matters that affect their health.
After all, every parent of a vaccine-injured child was once pro-vaccination.
In addition to the genetically modified ingredients in the vaccines being injected into babies, here are a few more disgusting ingredients they contain as well:

Disgusting Ingredient #1: Cells From Aborted Fetus

Aborted fetal cells, listed on vaccine package inserts as “Human Fetal Diploid Cells.” Two aborted fetal cell lines have been grown under laboratory conditions since the 1960s.
Pro-pharma outlets claim that only these two fetal cell lines are used, which is an outright lie. The two cell lines that have been admitted to be used in vaccines are:

1. WI-38 cell line (US): a human diploid fibroblast cell line derived from a three month old fetus aborted “therapeutically” because the family felt they had too many children.
2. MRC-5 cell line (UK): a cell line derived from lung fibroblasts of a 14 week old fetus due to “psychiatric” issues with the 27 year old mother.

Eye tissue from a 21 week old fetus is currently used in flu shots, as well as experimental vaccines for malaria and cancer, and Merck’s PER.C6 cell line, derived from the eye tissue of an 18 week old fetus, is the cell line used in many of the 271 vaccines in the CDC’s pipeline.
Terms to Investigate: PERC6, MRC5, WI-38, HEK-293
Which Vaccines? Adenovirus vaccine, DTaP vaccine, Hep A vaccine, Hep B vaccine, MMR vaccine, Rabies vaccine, Varicella (Chickenpox) vaccine

Disgusting Ingredient #2: Serum From Aborted Calf Fetus Blood

One of the more grotesque methods involved in vaccine manufacturing is the collection of fetal bovine serum. The purpose for serum is providing a nutrient broth for viruses to grow in cells.
How is the blood collected?
According to the Humane Research Australia website:
“After slaughter and bleeding of the cow at an abattoir, the mother’s uterus containing the calf fetus is removed during the evisceration process (removal of the mother’s internal organs) and transferred to the blood collection room. A needle is then inserted between the fetus’s ribs directly into its heart and the blood is vacuumed into a sterile collection bag. This process is aimed at minimizing the risk of contamination of the serum with micro-organisms from the fetus and its environment. Only fetuses over the age of three months are used otherwise the heart is considered too small to puncture.
Once collected, the blood is allowed to clot at room temperature and the serum separated through a process known as refrigerated centrifugation.”

A 7-Pound Premature Baby Died After Receiving 8 Vaccine Doses, Her Death Was Blamed On Co-Sleeping Instead Of The Toxic Vaccines
In Louisiana, another infant has died following routine vaccinations. Aysia Hope Clark was born nearly a month and a half premature. When she was six weeks old, her doctor detected a heart murmur. He then had the nurse administer eight vaccine doses into her tiny little body.
Ten days later, which is a critical time children die from vaccine-related injuries, Aysia stopped breathing, her heart stopped beating and she died while sleeping on her mother’s arm. [1,2]
The pathologist’s opinion was that Aysia died from positional asphyxiation related to co-sleeping and being born prematurely, without having to prove this is what she died from. There was no mention on her autopsy report that she had been recently vaccinated.
Aysia’s parents, Hope Doucet and Joseph Clark, were informed the burden of proof was shifted onto them, to prove Aysia died from the vaccines and that it would be nearly impossible to receive any compensation from the National Vaccine Injury Compensation Program.
In the State of Louisiana, three types of vaccine exemptions are offered for children to go to school unvaccinated: medical, religious and philosophical. This family will no longer vaccinate after losing their baby and learning they are the ones held responsible when the vaccines harm. [3]
Hope is now well aware that vaccinations are the hidden cause of infant mortality, after witnessing her own daughter’s death get covered up. She courageously shares her true story about what happened to her daughter, in hopes to help educate other parents about the importance of researching vaccines before blindly trusting what the doctor tells you.

The Lies About The Vitamin K Shot
By Paul Webber – September 1, 2016
courtney charles – Vitamin K is scheduled to be injected into babies within an hour of birth. One of their assaults out of the womb and most parents allow it. It’s a vitamin that we are told will save our baby’s life from the deficiency they are born with, so of course we would agree to it. But only because we are fed lies.
First, it is a lie that it is needed. Listen to this fear campaign delivered by the CDC:
“Babies are born with very little vitamin K stored in their bodies. This is called “vitamin K deficiency” and means that a baby has low levels of vitamin K.  Without enough vitamin K, babies cannot make the substances used to form clots, called ‘clotting factors.’  When bleeding happens because of low levels of vitamin K, this is called “vitamin K deficiency bleeding” or VKDB. VKDB is a serious and potentially life-threatening cause of bleeding in infants up to 6 months of age. A vitamin K shot given at birth is the best way to prevent low levels of vitamin K and vitamin K deficiency bleeding (VKDB).…waiting to see if your baby needs a vitamin K shot may be too late.  Babies can bleed into their intestines or brain where parents can’t see the bleeding to know that something is wrong. This can delay medical care and lead to serious and life-threatening consequences. All babies are born with very low levels of vitamin K because it doesn’t cross the placenta well. Breast milk contains only small amounts of vitamin K. That means that ALL newborns have low levels of vitamin K, so they need vitamin K from another source.  A vitamin K shot is the best way to make sure all babies have enough vitamin K. Newborns who do not get a vitamin K shot are 81 times more likely to develop severe bleeding than those who get the shot.”
How has humanity survived all this time without this shot? Vitamin K does pass through the placenta, it does get passed through breast milk, and moms eating plenty leafy greens, veggies, fruits, and oils are passing plenty to their babies. Interesting however that certain medications can interfere with vitamin K and deplete it or cause other clotting and bleeding issues. If mom is on IV antibiotics (often the case if she is Group B strep positive during the birth), certain pain medication, or had recent vaccines it could deplete her vitamin K levels or pass through to the baby and deplete the baby’s vitamin K levels. Want to know another thing that could cause bleeding disorders in babies unrelated to the “need” for vitamin K? The Hepatitis B vaccine, also scheduled to be given within 12 hours of birth. Actually, most vaccines have the same adverse reaction listed in the package inserts, also called thrombocytopenia or ITP.  So maybe if we stopped vaccinating babies they wouldn’t be bleeding to death.
Beyond the lie that it is necessary is the lie that it is just a safe and harmless vitamin. Here it is, the bold-faced lie in print:
“Yes, the vitamin K shot is safe. Vitamin K is the main ingredient in the shot. The other ingredients make the vitamin K safe to give as a shot.”
The manufacturer disagrees, this is in the insert:
“Severe reactions, including fatalities, have also been reported following INTRAMUSCULAR administration.”

Aidan Quinn, the father of a vaccine-injured child, doesn’t pull any punches . . .
>>> Educate before you vaccinate!!! tiny.cc/FreeVaccinationEducation
Networking, exemption information and doctor resources: tinyurl.com/RevolutionForVaccineChoice
Follow us: facebook.com/RevolutionForChoice
Read all vaccine inserts: tinyurl.com/ReadTheVaccineInsert
#RevolutionForChoice #InformedConsent #EducateBeforeYouVaccinate #VAXXED #VaccineInjury #Autism

This Vaccine Has Killed Young Women And Is Still On The Market
Common Adverse Reactions
Aside from the questioned efficacy of Gardasil, this vaccine has some nasty verified side effects that will make your jaw drop.

These are the most common adverse reactions listed following the first dose of Gardasil in boys:
    Headache
    Pyrexia
    Oropharyngeal pain
    Diarrhea
    Nasopharyngitis
    Nausea
    Upper respiratory tract infection
    Upper abdominal pain
    Myalgia
    Dizziness
    Vomiting
These are the most common adverse reactions listed following the first dose of Gardasil in girls:
    Pyrexia
    Nausea
    Dizziness
    Diarrhea
    Vomiting
    Cough
    Toothache
    Upper respiratory tract infection
    Malaise
    Arthralgia
    Insomnia
    Nasal congestion
Other Adverse Reactions Listed On Insert (male and female):
    Pelvic inflammatory disease
    Urinary tract infection
    Pneumonia
    Pyelonephritis
    Pulmonary Embolism
    Asthma
    Death*
    Sepsis
    Pancreatic cancer
    Arrhythmia
    Pulmonary tuberculosis
    Hyperthyroidism
    Acute renal failure
    Traumatic brain injury
    Cardiac arrest
    Systemic lupus erythematosus
    Cerebral vascular accident
    Breast cancer
    Nasopharyngeal cancer
    Asphyxia
    Acute lymphocytic leukemia
    Chemical poisoning
    Myocardial ischemia
    Miscarriage (female)
    Premature menopause (female)

*Here’s a video compilation of the unfortunate fatalities caused by Gardasil:

Senator Paid $400,000 By Pharma Pushes Mandatory Vaccine Law
As is the case with New York state sendator, Kemp Hannon. Hannon took over $400, 00 from pharmaceutical companies. He also has pushed for a menengitis vaccine law that would make the vaccine mandatory for 7th to 12 graders.
Via New York Daily News – http://www.nydailynews.com/news/politics/lovett-heath-pol-big-money-drug-firms-article-1.2449907
Lovett: Health Committee pol raises eyebrows with investments in drug firms
Sen. Kemp Hannon (R-Nassau County) in 2014 invested in 14 companies that would fall under his committee’s purview.
By comparison, Assembly Health Committee Chairman Richard Gottfried (D-Manhattan) did not report owning any stock in health-related companies.
In addition to his investments, Hannon over the past four years also received more than $420,000 from pharmaceutical and other medical interests, records show.
Hannon’s office had no comment. On the part of his 2014 state financial disclosure form dealing with investments, he wrote that sales and purchases were ‘at sole discretion of the broker.’

A book written in 1889 called 45 years of Registration Statistics, Proving Vaccination to be both useless and dangerous.
It covers 45 years (so starting in the year 1844) 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 VERSES the UNvaccinated…..bad news for the vaccinated…they were dying more from other diseases such as measles, mumps, smallpox and diphtheria because of a weakened countenance from vaccines.
https://archive.org/stream/b2136140x#page/n0/mode/2up
PDF source: https://ia802703.us.archive.org/31/items/b2136140x/b2136140x.pdf

The medical textbook definition of a vaccine adverse reaction: Brain Infection (Merck Manual)
Here is the definition of a vaccine adverse reaction from the largest selling medical textbook, the Merck Manual (see below), filed under their category of brain, spinal cord and nerve disorders: brain infections.
The brain infection caused by vaccines is encephalitis.
Encephalitis is inflammation of the brain. Patients who suffer encephalitis can be left with physical disabilities, mental deterioration and persistent cognitive dysfunction – which matches the definition of autism.
Vaccines can cause encephalitis and encephalitis can cause autism.
Below the following text is a list of ten vaccine package inserts that have the brain infection encephalitis as an adverse reaction.
Below that are medical journal references to vaccine-induced encephalitis and mental deterioration and disability after encephalitis.
At the very bottom of this page are articles describing secret multi-million dollar US government compensation payments to children that suffered vaccine-induced encephalitis and who are now autistic.

Encephalitis
By John E. Greenlee, MD, Neurology Service, George E. Wahlen VAHCS, Salt Lake City;Department of Neurology, University of Utah School of Medicine

Encephalitis is inflammation of the brain that occurs when a virus directly infects the brain or when a virus, vaccine, or something else triggers inflammation. The spinal cord may also be involved, resulting in a disorder called encephalomyelitis.

Largest Ever Vaccine Autism Payout: Family Receive $20 Million – Media Blackout
May 28, 2017 Sean Adl-Tabatabai
The largest ever vaccine-autism payout in U.S. history has received little to no coverage by the mainstream media, despite the fact that it proves once and for all that vaccines can cause autism.
In a landmark ruling, Hannah Poling is set to receive $1.5 million dollars for her life care; lost earnings; and pain and suffering for the first year. In addition, the family will receive over $500,000 per year to pay for Hannah’s care. The overall compensation is likely to amount to $20 million over the rest of the child’s lifetime.
CBS News reports: Hannah was described as normal, happy and precocious in her first 18 months.
Then, in July 2000, she was vaccinated against nine diseases in one doctor’s visit: measles, mumps, rubella, polio, varicella, diphtheria, pertussis, tetanus, and Haemophilus influenzae.
Afterward, her health declined rapidly. She developed high fevers, stopped eating, didn’t respond when spoken to, began showing signs of autism, and began having screaming fits. In 2002, Hannah’s parents filed an autism claim in federal vaccine court. Five years later, the government settled the case before trial and had it sealed. It’s taken more than two years for both sides to agree on how much Hannah will be compensated for her injuries.
In acknowledging Hannah’s injuries, the government said vaccines aggravated an unknown mitochondrial disorder Hannah had which didn’t “cause” her autism, but “resulted” in it. It’s unknown how many other children have similar undiagnosed mitochondrial disorder. All other autism “test cases” have been defeated at trial. Approximately 4,800 are awaiting disposition in federal vaccine court.

It is estimated that Vioxx killed more U.S. citizens than the Vietnam War. If a single pharmaceutical company can’t admit that was a problem, how is anyone ever going to be able to face the reality of what vaccines have done to our population?
Shares work better than likes!
T-Shirts, Hats, Books and more!
http://myincredibleopinion.com
All video episodes on YouTube: https://www.youtube.com/c/MyIncredibleOpinionWithForrestMaready

83 Cases of Autism Associated with Childhood Vaccine Injury Compensated in Federal Vaccine Court
10 May, 2011, 12:13 ET from SafeMinds
For over 20 years, the federal government has publicly denied a vaccine-autism link, while at the same time its Vaccine Injury Compensation Program (VICP) has been awarding damages for vaccine injury to children with brain damage, seizures and autism. A new investigation, based on verifiable government data, breaks ground in the controversial vaccine-autism debate. The investigation found that a substantial number of children compensated for vaccine injury also have autism and that such cases have existed since 1989, the year after the VICP was formed.
SafeMinds’ Executive Director, Lyn Redwood, RN, MSN comments, “This study dramatically shifts the debate on autism and vaccines.  The question is no longer, Can vaccines cause autism? The answer is clear.  Now, we have to ask, How many cases of autism have vaccines caused and how do we prevent new injuries from occurring?”  The government has asserted that it “does not track” autism among the vaccine-injured.  SafeMinds responds that not looking is the easiest way not to find something.  SafeMinds is calling for immediate federal research into the mechanisms of injury in these children in an effort to protect other children from harm and Congressional action to reform the VICP.
The peer-reviewed study looked at cases of vaccine injury that have been monetarily compensated by the federal Vaccine Injury Compensation Program.  It was published today in the Pace Environmental Law Review.  The study investigated approximately 1300 cases of childhood brain injury as a result of vaccines in which the Special Masters ruled for the plaintiffs, looking for references to autism, symptoms of autism or disorders commonly associated with autism. It reports that twenty-one cases actually stated “autism or autism-like symptoms” in the court records.  The researchers then identified and contacted 150 more compensated families to find out whether the children had autism.  They were able to find an additional 62 cases (greater than 40% of their sample) for a total of 83 cases of autism.  In 39 cases (47%) there was confirmation of autism beyond parental report.

 

Just News – The Alex Jones Channel – Millie Weaver Spills On California Blood Prostitutes

Navy SEAL Confirms: Thousands of Elite Pedophiles Arrested – Media Blackout Mainstream media ignores elite pedophilia ring arrests
By: Jay Greenberg  |@NeonNettle on 1st May 2017 @ 9.28am
As the blanket mainstream media blackout of Elite pedophile rings continues, a US Navy SEAL has gone on record to confirm thousands of high-ranking child abusers have been arrested, despite press silence on the busts.Retired SEAL, Craig Sawyer, has vowed to tackle the pedophilia networks in Washington D.C. head on and says that Trump’s promise to take down Pedogate is being fulfilled – it’s just being covered up.Sawyer has been working with high-level federal law enforcers and intelligence workers to conduct his own independent research, that has led him to discover that top government officials routinely torture and kill young children during satanic rituals.

Canadian Muslimah Explains Why Pedophilia is OK for Muhammedans

The Alex Jones Channel – Millie Weaver Spills On California Blood Prostitutes

Red Sea: Archaeologists Discover Remains of Egyptian Army From the Biblical Exodus
Suez| Egypt’s Antiquities Ministry announced this morning that a team of underwater archaeologists had discovered that remains of a large Egyptian army from the 14th century BC, at the bottom of the Gulf of Suez, 1.5 kilometers offshore from the modern city of  Ras Gharib. The team was searching for the remains of ancient ships and artefacts related to Stone Age and Bronze Age trade in the Red Sea area, when they stumbled upon a gigantic mass of human bones darkened by age.
The scientists lead by Professor Abdel Muhammad Gader and associated with Cairo University’s Faculty of Archaeology, have already recovered a total of more than 400 different skeletons, as well as hundreds of weapons and pieces of armor, also the remains of two war chariots, scattered over an area of approximately 200 square meters. They estimate that more than 5000 other bodies could be dispersed over a wider area, suggesting that an army of large size who have perished on the site.
This astounding discovery brings undeniable scientific proof that one the most famous episodes of the Old Testament was indeed, based on an historical event. It brings a brand new perspective on a story that many historians have been considering for years as a work of fiction, and suggesting that other themes like the “Plagues of Egypt” could indeed have an historical base.

 

 

Vaccine News – A study from West Africa’s Guinea-Bissau discovered that all-cause infant mortality more than doubled after the introduction of the DTP vaccination

The Alex Jones Channel – Shocking! Elmo Lies To Children About Vaccine Safety / Laughs At Autistic Victim

The First 6 Years Of A Fully Vaccinated Child’s Life Looks Like This…
We want you to have a choice. We want you to always know the facts. No laws should govern your child’s medical decisions, only you should.
Here is a comprehensive list of what your child receives if you fully vaccinate them for the first six years of their life.
Source: “What The Pharmaceutical Companies Don’t Want You To Know About Vaccines” – By Dr. Todd M. Elsner. Todd’s book is available on Amazon here.
Dr. Tenpenny’s Book is currently available on Amazon

17,500 mcg 2-phenoxyethanol (antifreeze)
5,700 mcg aluminum (neurotoxin)
Unknown amounts of fetal bovin serum(aborted cow blood)
801.6 mcg formaldehyde (carcinogen, embalming agent)
23,250 mcg gelatin (ground up animal carcuses)
500 mcg human albumin (human blood)
760 mcg of monosodium L-glutamate (causes obesity & diabetis)
Unknown amounts of MRC-5 cells (aborted human babies)
Over 10 mcg neomycin (antibiotic)
Over 0.075 mcg polymyxin B (antibiotic)
Over 560 mcg polysorbate 80 (carcinogen)
116 mcg potassium chloride (used in lethal injection)
188 mcg potassium phosphate (liquid fertilizer agent)
260 mcg sodium bicarbonate (baking soda)
70 mcg sodium borate (Borax, used for cockroach control)
54,100 mcg of sodium chloride (table salt)
Unknown amounts of sodium citrate (food additive)
Unknown amounts of sodium hydroxide (Danger! Corrosive)
2,800 mcg sodium phosphate (toxic to any organism)
Unknown amounts of sodium phosphate monobasic monohydrate (toxic to any organism)
32,000 mcg sorbitol (Not to be injected)
0.6 mcg streptomycin (antibiotic)
Over 40,000 mcg sucrose (cane sugar)
35,000 mcg yeast protein (fungus)
5,000 mcg urea (metabolic waste from human urine)
Other chemical residuals

What The Pharmaceutical Companies Don’t Want You To Know About VACCINES… Paperback – 2009
This book is a must read for parents, soon to be parents and physicians who regularly administer vaccines. There are over 500 pages of information proving that vaccines are not responsible for the eradication of communicable disease; vaccines have done nothing but promote chronic disease and illness; and vaccines contain the most toxic chemicals known to man. Furthermore, there are close to 2,000 references that back up the information in this book. The references are from studies published in peer reviewed medical journals, the Centers for Disease Control and Prevention, the Food and Drug Administration, the prestigious Institute of Medicine, and from the United States Congressional Reform Committee. Lastly, this book contains all the U.S. licensed vaccines and the ingredients each vaccine contains. The ingredients of each vaccine come directly from the pharmaceutical companies’ vaccine package insert which are cross referenced with the National Library of Medicine for their human health effects-You will be SHOCKED at the side effects these vaccine ingredients have on the human body! FACT: If anyone from the medical community wants to argue with the information in this book, they will argue among themselves-it is their information!

Ever wonder WHY we NEED a religious exemption from vaccines?
Are you aware that some vaccines are made from ABORTIONS?
Marcella Piper-Terry explains in detail how abortions are used in vaccine manufacturing and the implications of that.
Interview by Polly Tommey and camera by Joshua Coleman and Anu Vaidya with editing by Joshua Coleman.

#RFKCommission #Vaxxed

Countless teenage girls suffer paralysis, blood clots, brain damage and chronic pain from force-vaccination of Gardasil’s HPV “shot in the dark”
Friday, March 17, 2017 by: S.D. Wells
(Natural News) A sexually transmitted disease called human papillomavirus (HPV) is the only form of cancer known to be contagious, but what the medical community won’t tell parents of teenagers and preteens is that HPV is easily defeated by a normal functioning immune system. Of the 120 or more different strains of HPV, only about 15 are carcinogenic, and the HPV vaccines, which have never been proven safe or effective in any clinical trials, literally take a shot in the dark at a couple of these strains, much like the haphazard flu shot administered every year to tens of millions of unsuspecting victims of neurological poisoning.
Still, the CDC and rogue hacks and shills from Big Pharma use scare tactics to all but force-vaccinate girls as young as 9-years-old with sodium chloride and two versions of the dormant HPV cancers hidden in protein and genetically modified organisms.
Scare tactics and medical propaganda con mothers into getting their young daughters jabbed with deadly neurotoxins
“You won’t be able to have children if you get cervical cancer.” “You can catch cancer from having sex and die.” “The shot will make you immune to cancer.” “The shot prevents cancer.” “You wanna have children later? You better get this shot.” The propaganda is mind-blowing, and it unfortunately works. It convinces parents to do the unthinkable: have their little girls (and boys) jabbed with some of the most dangerous carcinogens on earth to “prevent” a couple of strains of a rather benign, pre-cancerous STD. It doesn’t even make sense. What’s even worse is that the HPV vaccine’s protection effect wears off after a few years (as does the cancer itself under normal immune conditions), so what’s the use of taking the risk of getting jabbed with all these neurotoxins? Just how young are kids becoming promiscuous enough to worry about STDs anyhow?
More than 10,000 adverse events have been reported from victims of the HPV scam, including blood clots in the heart and lungs, anaphylactic shock, loss of muscle use and seizures. Most infections from HPV are benign and cleared rapidly by the human immune system and never progress to cervical cancer, or even precancerous lesions of the vagina, vulva or anus. No valid reason for administering the HPV vaccine has ever even been established.
Why are HPV vaccines, like Gardasil (made by Merck) and Cervarix (made by GSK) so dangerous? Answer: They’re made with “denatured” forms and fragmented strains of the virus, meaning the virus is weakened and can remain dormant for months, if not years, so if you do get the virus later, who’s to say you didn’t get it from the vaccine itself? No studies on this have ever been conducted, nor will they likely ever be. Plus, Gardasil contains aluminum, sodium chloride, polysorbate 80 and l-histidine, the latter of which interferes with the brain’s defenses against metal toxins. That means the aluminum has a heightened chance of crossing the blood/brain barrier. Got brain damage? No wonder. The following are just four examples of the hundreds (if not thousands) of girls permanently damaged by HPV vaccines.

Stronger More Toxic Gardasil Vaccine Approved by FDA: Will More Girls Suffer and Die?
March 23, 2017
Malfeasance is when a public official violates the public trust by performing an act that is wrongful, legally unjustified, or contrary to law. Nonfeasance is the failure to act where there is a duty to act. Misfeasance is conduct that is lawful but inappropriate. Perhaps, when it comes to the recent approval of Gardasil 9 all of these apply.
10 December 2014: The FDA approved the use of a reportedly “new and improved” version of Gardasil, which will be marketed as Gardasil 9. According to the FDA approval letter, this action was taken without consultation with VRBPAC (the Vaccines and Related Biological Products Advisory Committee) which is responsible for reviewing and evaluating data concerning the safety, effectiveness, and appropriate use of vaccines and related biological products.
The FDA approval letter, signed by Marion Gruber, Director of Office of Vaccines Research and Review CBER,  states the reason for bypassing the advice of VRBPAC writing:
”We did not refer your application to the Vaccines and Related Biological Products Advisory Committee because our review of information submitted in your BLA, including the clinical study design and trial results, did not raise concerns or controversial issues which would have benefited from an advisory committee discussion.”
So, the Office of Vaccines Research and Review, Center for Biologics Evaluation and Research (CBER) committee took it upon themselves to decide there were ”no concerns or controversial issues” regarding the approval of Gardasil 9?
This division of CBER decided there would be no benefit from ”an advisory committee discussion”?
According to their own mission statement, the FDA is ”responsible for protecting the public health by assuring the safety, efficacy and security of human and veterinary drugs, biological products, medical devices, our nation’s food supply, cosmetics, and products that emit radiation.”
The FDA, and all committees associated with the FDA, are public officials and therefore obliged to act in the public’s best interest particularly when it comes to health and safety issues.
Is bypassing advisory committee discussions regarding Gardasil 9’s potential safety and efficacy acting in the public’s best interest, or is it malfeasance, nonfeasance and/or misfeasance?
Gardasil 9 Facts: More than DOUBLE the amount of Toxic Aluminum!
CBER decided there was no need for VRBPAC to review or evaluate any data concerning the safety, effectiveness, and appropriate use of Merck’s proposed Gardasil 9 vaccine before making a decision to approve the nine-valent HPV vaccine. This move is particularly disturbing when one considers the worldwide controversy surrounding Gardasil’s safety, effectiveness and appropriate use.

Studies about the aluminium toxicity on humans
Gardasil 9 insert
Gardasil insert

Dr. Yehuda Shoenfeld says vaccines cause auto-immunity. It’s really not a question of “IF” there are adverse events from vaccines, it’s a question of “how often?”, “how severe?”, and whether it’s worth the trade-off? You can listen to the pre-eminent expert on vaccine-induced autoimmunity in the world, or you can go to your mainstream pediatrician who will tell you that vaccines have “no risk, lots of benefits.” It’s really up to you!
This is just a clip from his talk, entire talk in comments below, as well as Dr. Shoenfeld’s new TEXTBOOK, called “Vaccines and Autoimmunity”!
By the way, “autoimmunity” includes all the crazy epidemics in our kids that weren’t around in the 1980s or earlier: asthma, food allergies, skin rashes, etc. “Some of the main examples of autoimmune disorders include diabetes mellitus type 1 (IDDM), systemic lupus erythematosus (SLE), Hashimoto’s thyroiditis, Graves’ disease of the thyroid, Sjögren’s syndrome, Churg-Strauss Syndrome, Coeliac disease, rheumatoid arthritis (RA), and idiopathic thrombocytopenic purport.”
Listen to Dr. Shoenfeld: “Dr. Yehuda Shoenfeld is on the editorial board of 43 journals in the fields of rheumatology and autoimmunity and is the founder and editor of the Israel Medical Association Journal, the representative journal of science and medicine in the English language in Israel. He is also is the founder and editor of “Autoimmunity Reviews” and co-editor of “The Journal of Autoimmunity”. His clinical and scientific works focus on autoimmune and rheumatic diseases, and he has published more than 1700 papers in journals such as the New England Journal of Medicine, Nature, the Lancet, the Proceedings of the National Academy of Sciences of the United States of America, the Journal of Clinical Investigation, the Journal of Immunology, Blood, the Journal of the Federation of American Societies for Experimental Biology, the Journal of Experimental Medicine, Circulation, Cancer, and others, and his articles have had over 31,000 citations. He has written more than three hundred and fifty chapters in books, and has authored and edited 25 books.”

A study from West Africa’s Guinea-Bissau discovered that all-cause infant mortality more than doubled after the introduction of the DTP vaccination.
An observational study from the West African country Guinea-Bissau titled, “The Introduction of Diphtheria-Tetanus-Pertussis and Oral Polio Vaccine Among Young Infants in an Urban African Community: A Natural Experiment,” [i] examined the introduction of diphtheria-tetanus-pertussis (DTP) and oral polio vaccine (OPV) in an urban community in Guinea-Bissau in the early 1980s. The World Health Organization introduced the Expanded Program on Immunization (EPI) in low-income countries in the 1970s with the goal of universal immunization for all children. In the introduction, the study’s authors state, “Except for the measles vaccines, surprisingly few studies examined the introduction of vaccines and their impact on child survival.”
The purpose of the study was to examine what happens to child survival when DTP and OPV were introduced in low-income countries. A community study [ii] of the state of nutrition and family structure found that severe malnutrition was not evident in urban Guinea-Bissau although it was initially assumed to be the main cause of the under-five mortality rate.
The study findings emerged from a child population that had been followed with 3-monthly nutritional weighing sessions since 1978. From June 1981 DTP and OPV were offered from 3 months of age at these sessions. Due to the 3-monthly intervals between sessions, the children were allocated by birthday in a ‘natural experiment’ to receive vaccinations early or late between 3 and 5 months of age. The study included children who were greater than 6 months of age when vaccinations started and children born until the end of December 1983. The researchers compared mortality between 3 and 5 months of age of DTP-vaccinated and not-yet-DTP- vaccinated children in Cox proportional hazard models.
When mortality was compared, the mortality hazard ratio (HR) among 3-5-month-old children having received the DTP (±OPV) was 5.00 compared with not-yet-DTP-vaccinated children [i.e. a 400% increase]. According to the authors, differences in background factors did not explain the effect. All-cause infant mortality after 3 months of age increased after the introduction of these vaccines (2.12 (1.07–4.19)) [i.e. a 212% increase]. However, the study findings revealed the negative effect was particularly strong for children who had received DTP-only and no OPV (10.0 (2.61–38.6)).
The researchers concluded:
“DTP was associated with increased mortality; OPV may modify the effect of DTP.”

Study – The Introduction of Diphtheria-Tetanus-Pertussis and Oral Polio Vaccine Among Young Infants in an Urban African Community: A Natural Experiment
Abstract
Background
We examined the introduction of diphtheria-tetanus-pertussis (DTP) and oral polio vaccine (OPV) in an urban community in Guinea-Bissau in the early 1980s.
Methods
The child population had been followed with 3-monthly nutritional weighing sessions since 1978. From June 1981 DTP and OPV were offered from 3 months of age at these sessions. Due to the 3-monthly intervals between sessions, the children were allocated by birthday in a ‘natural experiment’ to receive vaccinations early or late between 3 and 5 months of age. We included children who were <6 months of age when vaccinations started and children born until the end of December 1983. We compared mortality between 3 and 5 months of age of DTP-vaccinated and not-yet-DTP-vaccinated children in Cox proportional hazard models.
Results
Among 3–5-month-old children, having received DTP (±OPV) was associated with a mortality hazard ratio (HR) of 5.00 (95% CI 1.53–16.3) compared with not-yet-DTP-vaccinated children. Differences in background factors did not explain the effect. The negative effect was particularly strong for children who had received DTP-only and no OPV (HR = 10.0 (2.61–38.6)). All-cause infant mortality after 3 months of age increased after the introduction of these vaccines (HR = 2.12 (1.07–4.19)).
Conclusion
DTP was associated with increased mortality; OPV may modify the effect of DTP.