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Vaccines trigger a "cytokine
storm" of the immune system, leading to severe and permanent
neurological disorders, brain injuries and autism.
As vaccinepapers.org
writes:
The term “immune activation”
describes the activation of the cellular components of the immune
system. The developing brain can be injured by immune activation,
with life-long consequences (Meyer 2009, Deverman 2009, Estes 2016,
neusel 2014, Careaga 2017, Meyer 2014). Immune activation injury is
linked to autism, schizophrenia, depression and other mental
illnesses or neurodevelopmental disorders. Immune activation effects
on the brain are mediated by immune system signaling molecules,
especially cytokines (Estes 2016, Meyer 2014, Smith 2007, Choi 2016,
Pineda 2013).
Human brain development is
controlled by immune-system signals (i.e. “cytokines”).
Activation of the immune system during brain development causes
disruptions in these signals, resulting in permanent brain injury.
The injury manifests as autism, schizophrenia and other mental
illnesses. Adverse vaccine reactions are proven to stimulate a
cytokine (interleukin-6) proven to cause autism.
In the maternal immune activation
experiments, inflammatory signaling and some cytokines (e.g. IL-6)
traverse the placenta into the fetus. Consequently, immune activation
in the mother causes immune activation and elevated cytokines in the
fetus, and in the fetal brain (Oskvig 2012, Ghiani 2011).
Diverse evidence indicates that the
brain can be adversely affected by postnatal immune activation.
Postnatal immune activation experiments, human case reports, and
consideration of brain development timelines suggest that the human
brain is vulnerable to immune activation injury for years after
birth.
Postnatal immune activation can
have adverse neurological effects, including increased seizure
susceptibility (Chen 2013,Galic 2008), learning and memory deficits
(Harre 2008), and an increase in excitatory synapse formation (Shen
2016). Seizure disorders, learning and memory dysfunction, and
elevated excitatory signaling are associated with autism.
The timing of brain development
processes in humans supports the idea that the human brain is
vulnerable to immune activation and cytokines in the first few years
after birth, when vaccines are administered. Disruption of
synaptogenesis by vaccine induced immune activation is a particular
concern. The accumulating evidence indicates
that vaccine-induced immune activation, and aluminum adjuvants in
particular, may cause mental illnesses and neurodevelopmental
disorders, including autism.
Link to the paper: vaccinepapers.org/review-paper-al-adjuvant-autism-20-pages-97-references/
Peer-reviewed studies that found a causal link between aluminium in childhood vaccines and severe neurological disorders including autism:
Link: http://thinktwice.com/studies_aluminum.htm
Also read the following brief papers on the neurotoxicity of aluminium in vaccines:
Link: http://www.jpands.org/vol21no4/miller.pdf
Link: http://thinktwice.com/aluminum.pdf
Highest Level of Aluminium Found in Brain of Autistic Children (Study)
The following recently published landmark and highly alarming peer-reviewed study has found the highest levels of aluminium in the brain of 5 autistic children:
Link: http://info.cmsri.org/aluminum-and-your-health-blog/study-finds-some-of-the-highest-values-for-aluminium-in-human-brain-tissue-yet-recorded-in-brains-of-autistic-patients
CDC childhood vaccine schedule linked to neurological disorders and autism
The 2017 US CDC (Centre for Disease CREATION and PROMOTION) vaccine
schedule requires U.S. children from birth to age 6 to receive 50 doses
of 14 vaccines, many of which contain both neurotoxic aluminium and mercury (thimerosal)! Infants in the US are exposed from birth to age 2, to 24
vaccine doses, combining 8-in-1 vaccines to be given to infants 2, 4,
and 6 months in a single visit! Babies receive 36 vaccine doses before
they are 18 months old!
THIS IS CRIMINAL INSANITY & STATE-SANCTIONED MEDICAL MURDER OF NEWBORNS, INFANTS AND CHILDREN!
Link to CDC vaccine ingredients: https://www.cdc.gov/vaccines/vac-gen/additives.htm
Link to CDC vaccine schedule: https://www.nvic.org/CMSTemplates/NVIC/pdf/49-Doses-PosterB.pdf
Exponential increase in autism rates in US children linked to CDC vaccine schedule
In 1985, the autism prevalence rate in the US was 1 in 2,500; in 1995 it was 1 in 500; In 2014 it was 1 in 45! In children aged 3 to 17, the autism prevalence rate increased by 80% from 2011-2013! At this rate, it is predicted that 1 out of 2 children in the US will have autism by 2030!
A report by EPA scientists Timing of Increased Autism Disorder Cumulative Incidence analyzed the cumulative incidence of autistic disorder during a 10-year period (1987–1996) pinpointed a sharp “changepoint” year (1988) when the incidence of autism sharply increased. The “changepoint” year is concomitant with the year childhood vaccination schedules expanded.
Source: http://ahrp.org/disconnect-between-evidence-cdc-claims-re-childhood-vaccination-schedule/
Causal link between mercury (thimerosal) contained in vaccines, neurological disorders and autism
Scientific research and CDC internal documents on the toxicity of mercury (thimerosal) in vaccines reveal exposure to thimerosal during the first month of life increased the relative risk of autism by 7.6 (760%), 1.8 (180%) increased relative risk for a neurodevelopmental disorder; 2.1 (210%) relative risk for speech disorder; and 5-fold (500%) increased relative risk for a nonorganic sleep disorder. CDC also suppressed the original findings of another of its own studies that found a 340% (3.6) relative increased risk of autism for African American male babies following MMR vaccination in accordance with the CDC-recommended Childhood Vaccination Schedule.
The alarming and damning scientific evidence documents that infants exposed to vaccines laced with thimerosal during the first month of life are at alarmingly high increased the relative risk of serious harm. “The data on its toxicity (shows) it can cause neurologic and renal toxicity, including death," writes Dr. Richard Johnston, M.D., an immunologist and pediatrician from the University of Colorado.
Dr. Verstraeten also said: “what I will present to you is the study that nobody thought we should do.” The study categorized the cumulative effect of thimerosal-containing vaccines administered to infants after one month of life and assessed the subsequent risk of degenerative and developmental neurologic disorders, and renal disorders before the age of six. Dr. Verstraeten stated that ALL of these relative risks were statistically significant.
Source: http://ahrp.org/betrayal-of-public-trust-institutional-corruption-vaccine-safety-ratings-vaccine-science-falsified/
Additional published peer-reviewed studies that found a causal link between childhood vaccines containing mercury (Thimerosal) and neurological disorders including autism:
Link: http://thinktwice.com/studies_autism.htm
Synergistic Toxicity of Aluminium & Thimerosal in Vaccines
Dr. Boyd Haley, former professor of medicinal chemistry and chairman of the chemistry department at the University of Kentucky, published a study in which he investigated the effect of combining aluminum hydroxide with thimerosal. In this study, cultured neurons showed no significant cell death six hours after they were exposed to just aluminum; more than 90% survived. Thimerosal alone also caused few neurons to die after six hours of exposure. Again, more than 90% survived. However, when cultured neurons were exposed to aluminum and thimerosal, only about 40% survived after six hours, clearly demonstrating synergistic toxicity (Figure 3). Source: http://www.jpands.org/vol21no4/miller.pdf
As Neil Miller writes:
" Millions of children every year are injected with vaccines containing mercury and aluminum despite well-established experimental evidence of the potential for additive or synergistic toxicity when an organism is exposed to two or more toxic metals. Dr. Haley’s study in which cultured neurons died at an accelerated rate following concurrent exposure to aluminum and thimerosal provides evidence of an enhanced detrimental effect. In addition, aluminum toxicity levels published by FDA indicate that two-month-old babies who are vaccinated according to CDC guidelines may be receiving quantities of aluminum that are significantly higher than safety levels."
Statements from Prominent & Eminent Medical Doctors & Scientists on the Toxicity of Aluminium in Childhood Vaccines:
Conclusion:
Both neurotoxic aluminium and mercury (thimerosal) contained in multiple doses of childhood vaccines as well as the CDC vaccine schedule cause severe and permanent neurological disorders including autism in newborns, infants and children!
When will the US sanctioned Vaccine Holocaust of newborns, infants and children end ???????????????
Arya Vrilya
