…after parents refuse to vaccinate baby already harmed from vaccination.
On November 5, 2017, 26-year-old Texas Church Shooter Devin Kelley killed 26 people and injured about 20 more. His victims ranged in age from 18 months to 77 years old. From a very early age, Kelley was taking prescription psychotropic drugs. Fox News reported that a former middle school classmate said that Kelley would complain about his parents and medications during school. “His parents had him on high doses of ‘psych’ meds from 6th to 9th grade, the time I knew him,” said the student, who wished to be identified as Reid. ¤ The Daily Mail quoted Kelley’s best friend from ages 12 through 19, Ralph Martinez, who said Kelley was taking prescription drugs for “ADHD” and during a visit with him when Kelley was 21 the future killer was taking “medicine” for his “aggression.” §In 2012, Kelley was court-martialed by
VLA Comment: As usual a great booklet by CCHR. One thing missing though…
The details of why these drugs cause one individual to commit heinous acts of homicide but not such outrageous behavior in another….The ANSWER IS HERE…
How the anti-vaccine movement crept into the GOP mainstream (May 2019)
In Kentucky, Gov. Matt Bevin said vaccine mandates were un-American. In Oregon, the state party used vaccine mandates to bash Democrats as violating parental rights. And in the California Senate, all 10 Republicans last Wednesday opposed a measure aimed at stopping bogus medical exemptions from vaccination.
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