Yale University Study Using Children’s Health Records Links
Vaccines to Mental Disorders
Though the collaboration between researchers at Pennsylvania State University and the Yale Child Study Center yielded results that seem to dispute the safety of vaccines, the authors asserted that the study needs replication on a larger scale and does not establish a causal relationship between vaccines and neuropsychiatric disorders.
While only about 10 percent of children with open wounds had received vaccinations, vaccines had been given to over 20 percent of children later diagnosed with anorexia. Higher numbers of vaccinated children were also found among those who were diagnosed with OCD, anxiety disorder and ADHD as soon as three months after their vaccinations. READ MORE,,,
Despite the huge amount of money invested in studying vaccines, there are few observational studies and virtually no randomized clinical trials documenting the effect on mortality of any of the existing vaccines. One recent paper found an increased
hospitalization rate with the increase of the number of vaccine
doses and a mortality rate ratio for 5e8 vaccine doses to 1e4 vaccine
doses of 1.5, indicating a statistically significant increase of
deaths associated with higher vaccine doses. Since vaccines are
given to millions of infants annually, it is imperative that health
authorities have scientific data from synergistic toxicity studies on
all combinations of vaccines that infants might receive to improve
vaccine safety .
Moreover, from one side the non-specific beneficial effects of
vaccines on survival can be underestimated, on the other side the
negative effect of other vaccines may not be captured by current
studies . As a matter of fact, in case of vaccine-associated
autoimmune phenomena latency periods between the vaccine
administration and the appearance of clinical symptoms can be
longer (months or years after vaccination) than the time interval
This paper discusses the hypothesis of the ‘immune response gene network’ and genetic (and bioinformatic) strategies to study associations between immune responsegene polymorphisms and variations in humoral and cellular immune responses to prophylactic viralvaccines, such as measles–mumps–rubella, influenza, HIV, hepatitis B and smallpox.Immunogenetic studies reveal promising new vaccine targets by providing a better understanding of the mechanisms by which gene polymorphisms may influence innate and adaptive immune responses to vaccines, including vaccine failure and vaccine-associated adverse events.
The goal of pharmacogenomics and vaccinomics is to identify genetic variants that predict adverse responses to vaccines, predict aberrant immune responses, contribute to personalized therapy and that predict susceptibility to diseases and response to vaccines.
It is hard to believe that the establishment has known this relationship between polymorphism (the presence of genetic variation within a population) that will cause an adverse reaction from vaccines since 2009. And we just keep destroying all the emerging generations of mankind (and animals) What is not expressed in this paper is that ALL neonates and children not have the mature systems that address this assault.
Vaccines are a class of medicines that are being viewed under the pharmacogenomic microscope. Variations in genes involved in virus binding and cell entry, antigen recognition, processing and presentation, immune effector cell function and immunoregulation are all crucial in an individual’s ability to propagate a co-ordinated attack against an invading pathogen. Associations in response with genotype or phenotype have been recognised with vaccines against measles, mumps and rubella, influenza, HIV, Hepatitis B and smallpox.4
6.4. Modification of drug hepatic metabolism (cyp450)
Reports of patients developing phenytoin, warfarin or theophylline
toxicity, following acute infections [118,119] and anti-influenza vaccination,
have been published [119–128]. In one study, toxic elevations
in the levels of the concurrent medicines were reported to occur up to
28 days after vaccination . Other vaccines such as Bacillus Calmette
Guerin (BCG), and immunostimulators such as interferons and various
cytokines are able to produce the same effect [129–131]. The effect of
immunostimulation on drug metabolismwas demonstrated several decades
ago in laboratory animals, using several vaccines and adjuvants,
with the demonstration that cytochrome P450 hepatic enzyme inhibition
as a consequence immunostimulation is involved, leading to
reduced clearance of the concurrently administered medicines
[132–135]. Years later, Renton reported that the release of cytokines,
such as IL-1, IL-2, IL-6, TNF, TGF-β and IFNs, is involved in modulating
the expression of several P450 isoforms . Reversible changes in
the pharmacokinetic parameters of theophylline, and decreased expression
of CYP1A, 2B1/2, and 3A subfamily, have also been reported in rats
after intravenous injection of lipopolysaccharide (endotoxin) derived
from Klebsiella pneumoniae  and a similar effect was observed
after application of FCA to mice (used as a positive control), for comparison
with a non-toxic intranasal adjuvant called AFCo1 .
On the other hand, Prandota have shown the rapid decrease in the
total CYP450 liver content of FCA-treated rats and the selective downregulation
of specific CYP isoforms through a direct reduction in
mRNA levels (CYP2B, CYP2CI1, CYP3A1, and CYP2E1), protein content
(CYP2B, CYP2C11, and CYP2E1) and catalytic activity (CYP2C6,
CYP2C11, and CYP2E1). Thus, Prandota has highlighted that polymorphisms of drug-metabolizing enzymes and cytokines may contribute markedly to drug-induced hepatotoxicity and drug pharmacokinetic disturbances, affecting genetically predisposed subjects .
There is evidence that only between one and 10 percent of serious health problems that occur after use of prescription drugs or vaccines in the U.S. are ever reported to federal health officials, who are responsible for regulating the safety of drugs and vaccines and issue national vaccine policy recommendations.    
As of January 2, 2019, there have been 1,258 claims filed so far in the federal Vaccine Injury Compensation Program (VICP) for 82 deaths and 1,176 injuries that occurred after measles vaccination.
Of that number, the U.S. Court of Claims administering the VICP has compensated 483 children and adults, who have filed claims for measles vaccine injury. READ MORE…
This video summarizes the preliminary results of our analyzes, presented to the conference organized by the Italian National Biologist’s Chamber on January 25, 2019. After this public event, many of the preliminary results were confirmed with certified standard controls and inter-laboratory analysis, plus one was object of a notification to the police office responsable for the control of defective drugs on the market.
Scientists Find Chronic Brain Inflammation in Children With Autism
The concept that chronic inflammation is one of the hallmarks of ASD is not new. In 2013, the Journal of Neuroinflammation published an article stated that, “Increasing evidence indicates that brain inflammation is involved in the pathogenesis of neuropsychiatric diseases,” including ASD.
Pointing out that many children with ASD “regress at about age 3 years, often after a specific event such as reaction to vaccination, infection, trauma, toxic exposures, or stress,” the authors of that article go on to discuss increasing evidence of immune dysfunction/inflammation in ASD and to detail multiple markers of inflammation in the brains and cerebral spinal fluid of children with ASD.