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The study asserts that children of mothers who had two or more instances of flu had a doubled-risk of being diagnosed with autism prior to the age of 3; as well as simply having a fever. Also attributed to the development of autism in children were the uses of a pharmaceutical grade anti-biotic during pregnancy.
This study gives governmental agencies like the Centers for Disease Control and Prevention (CDC) an excuse to disregard scientific data correlating autism to the use of mercury-based preservatives like Thimerosal to the onset of autism. Other alarmist researchers claim these findings are "noteworthy" because of the extensive range of mother and children interviewed. The fact that the conclusions are bogus does not register with these so-called experts.
There were no differentiation between the wide range of possible infections that a pregnant woman could contract, nor the pharmacological drugs that would be prescribed to the pregnant woman by her doctor; yet there is an association between the contraction of flu and development of infantile autism.
Doctors are attempting to find any other answer to the problem of autism arising in children without centering their attention on the vaccines being given to both children and pregnant women.
In 1997, a study which proved the link between autism and vaccines was irgnored by the Food and Drug Administration (FDA) and suppressed by the CDC.
Laura Hewitson, Ph.D. and lead researcher, studied macaque monkeys that were given the exact same MMR vaccine as children in 1994 - 1999. The results entitled "Influence of pediatric vaccines on amydgala growth and opioid ligand binding in rhesus macaque infants: A pilot study" were published in Acta Neurobiological Experiments in 2010. This vaccine has the mercury based preservative Thimerosal.
Hewitson discovered that: "Vaccine-exposed and saline-injected control infants [monkeys] underwent MRI and PET imaging at approximately 4 and 6 months of age, representing two specific timeframes within the vaccination schedule . . . These results suggest that maturational changes in amygdala volume and the binding capacity of [11C]DPN in the amygdala was significantly altered in infant macaques receiving the vaccine schedule."
The research paper documented that there were significant biological changes and altered behaviors that occurred in the vaccinated monkeys that were identical to children diagnosed with ASD (autism).
Sufferers of autism develop a broad spectrum of symptoms ranging from:
- Mild social awkwardness
- Asperger's syndrome
- Profound mental retardation
- Debilitating repetitive behaviors
- Inability to communicate
The unvaccinated monkey exhibited no changes or symptoms whatsoever.
Dr. Bernadine Healy, who has read this study by Hewitson but did not participate in the research, made these remarks concerning the findings: "I think public health officials have been too quick to dismiss the hypothesis as 'irrational,' without sufficient studies of causation...without studying the population that got sick . . . I have not seen major studies that focus on 300 kids who got autistic symptoms within a period of a few weeks of the vaccines."
Mainstream doctors, defending the dangerous vaccines they administer to pregnant women claim that the mother's immune response system is somehow affecting the developing brain of their unborn fetus which results in the symptoms of autism in the early stages of childhood development.
In animal studies, it is observed that the mother's immune system, when fighting off infection, will negatively affect the child's brain in utero, while asserting that vaccines have nothing to do with the immune system response.
In 2003, a study came out of Denmark that showed that when doctors stopped using vaccines that contained the mercury-based Thimerosal, the incidents of autism began to dramatically reduce. When the study was published by the CDC, the agency changed the findings to say that the removal of Thimerosal was actually the direct cause of the rising autism rates.
The authors of the study contacted the CDC, regarding their change without the express permission of the authors prior to publication. An investigation concluded that the editors of the Journal were coerced by the CDC to print the revised data.
The danger associated with vaccines extends beyond the advent of autism. Vaccines being created now are done so with patented GMOs mixed with human DNA which creates broken information that are read by the cells of the body and directly translates to disease in the body.
The pandemic fear surrounds such genetically engineered bio-weapons such as the bird flu H5N1 that continually changes its make-up which is not a naturally occurrence. A propaganda study led by Ron Fouchier, professor from Erasmus Medical Center, researched which viruses would cause pandemics so that the pharmaceutical industry could get to work on focused vaccines and pressure governments to push them onto the general population.
Fouchier claimed that he proved H5N1 mutated naturally, although scientists analyzing the virus found that it is 3 different types of flu spliced together.
The scientific community is mounting evidence that vaccines are directly causational to the appearance of superbugs and bacteria that threaten the future of the human race. And what these researchers are calling for - more vaccines.
Scientists are finding that the whooping cough vaccine contributes to the colorization of the bacteria in the lungs. In real world observation, we are seeing a rise in whooping cough, despite the increased inoculations. Recently the Centers for Disease Control and Prevention (CDC) have come forward to war people about the dangers of pigs, contact with pigs and a new strain of swine flu that is most likely to affect children in the US.
The new strain is derived from the original virus which came to light in 2009. This shows the new type has been engineered; as it is an amplified version of the first.
Yes, you are stupid and we intend to prove it by getting you to believe this! I think that's what they are attempting to say. They are swine.