Vaccinations part 2

As we have noted, environmental medicine is diligently pursuing epigenetic investigations to better understand how exogenous chemicals and toxins affect the body’s immune system and genetic disposition. Simultaneously, epigenetics remains an anathema within the vaccine industry. This is because epigenetics is the vaccine industry’s greatest threat and may well be the harbinger of vaccination’s collapse in the future. For that reason, we increasingly observe the pro-vaccine community aggressively associating vaccine-injury illnesses with parental gene inheritance. Seeming vaccine injuries, the CDC informs us, are all due to inherited genes and are not stimulated by vaccine interference. More recently we are being told that genes associated with autism have always been present in the human genome.

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Yet, no one references the other body of research, such as a University of Montreal analysis, that has discovered the majority of these so-called autism genes are de novo.

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De novo genes are genetic mutations that appear for the first time in a parent’s germ cell or during the development of the fertilized egg itself. The most likely causal candidates accounting for de novo mutations are epigenetic. Consequently, a woman who is vaccinated during pregnancy will have her unborn child at a higher risk of de novo mutations due to the toxic stew of chemicals, additives, and viruses she was injected with. In order to skirt the evidence supporting this scientifically plausible hypothesis, the CDC and its minions in the vaccine industry mustcontinue to rely upon an older, determinist, and regressive view ofgenetics that denies epigenetic activity. Fortunately, this outdated genetic paradigm is rapidly being deconstructed and proven unsound by other scientific disciplines.

Other examples are Ehlers-Danlos Syndrome or EDS (a connective tissue disorder) and Osteogenesis Imperfecta (a disorder characterized by brittle bones). Both conditions are known inherited genetic disorders and associated with a series of identifiable gene mutations. And both illnesses are increasing at an alarming rate among young children and adolescents.

In 2014, Dr. Lloyd Phillips conducted independent research to determine why so many young adolescent and teenage girls were rapidly coming down with more serious expressions of EDS. His findings concluded that these otherwise healthy girls carried an EDS genetic marker which remained dormant until shortly after receiving the HPV vaccine or Gardasil.

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A similar discovery was made by Dr. Robert Kendall Endres in 2009, who noted in 1962 there were approximately 10,000 cases of brittle bone syndrome worldwide. By 1978 there were 836,000 cases and over 4 million in 2000. This increase parallels the rapid increase in the number of vaccinations recommended in the CDC’s vaccine schedule and the WHO’s global vaccination initiatives. Although both disorders are associated with certain inherited gene mutations, the plausibility of vaccination as the triggering culprit responsible for their expression and activation cannot be ruled out.

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Any one of the many vaccines on the market today can cause enormous genetic and epigenetic disruption in any human being. Epidemiologists are puzzled about why some people respond according to plan for any given vaccine and why others don’t. For example, only 10% of people receiving the MMR vaccine generate high levels of measles antibodies following vaccination while another 10% don’t respond at all. Dr. Gregory Polland at Mayo’s Vaccine Research Group realizes this is undoubtedly due to genetic mutations and an individuals’ genetic code.

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The one-size-fits-all vaccination policy now advocated by the CDC and its leading spokespersons such as Paul Offit therefore has no rational and sound basis in science.

Since 1996, the CDC’s vaccine divisions and the World Health Organization (WHO) have known they have a very serious health problem with genetic contamination in every vaccine that relies upon animal cell culturing. This is a very dark side of the vaccine industry’s manufacturing methodology. The fact that genetic contamination, much of which remains unknown and unidentified, is being injected into infants as young as 24 hours after birth receives absolutely no attention and is ignored by those who espouse political correctness on their provaccine posturing.

In the past we have reported on the primitive methodology that vaccine makers still utilize to culture the viruses that go into vaccines.

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In 1999, the FDA convened a non-public regulatory meeting to review the health hazards of undesirable viral DNA fragments and protein contamination in all vaccines relying on animal cell culturing. Concerns were particularly focused upon vaccines using fertilized chicken eggs: the influenza, MMR, and yellow fever vaccines. Among the most worrisome contaminants were prions (tiny proteins responsible for incurable diseases in both humans and animals), viral oncogenes capable of causing cancer, viral variants that might cause AIDS, and multiple known and unknown viruses present in the viruses’ culture medium. The executive scientists present acknowledged that recombination activity between viral codes and cells in the tissue culture is common and therefore the same can certainly occur in a child’s body after vaccination. 15 Again, Barbara Lo Fisher warns that “because viruses are constantly mutating and recombining with each other and scientists do not understand how viruses and genes interact, it is clear that what is not known about the effects on human health of widespread use of live virus vaccines is far greater than what is known.” 6

Current vaccine technology makes it impossible to filter out all genetic contamination and DNA debris from vaccine preparations. Therefore, the FDA has set weight limits on the amount of foreign genetic contamination permitted. Since vaccine manufacturers have been unable to meet these restrictions, the CDC has reduced the requirements to apply only to cancerous cell lines. Other DNA contamination allowances were increased one hundred-fold. According to the FDA’s industry guidelines on vaccine production, the removal of foreign DNA and protein contamination from vaccines employing human and animal cell lines is a “non-binding recommendation.”

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A recent example of a vaccine temporarily removed from the market by the FDA is Glaxo’s rotavirus vaccine Rotarix. In 2010, an independent California laboratory identified a foreign pig virus, porcine circovirus 1 or PCV1, present in Rotarix. The CDC immediately reported that this contaminant posed no risks, although babies as young 2 months old were being vaccinated with this swine virus contaminant. The laboratory also found avian leukosis virus in the MMR vaccine and monkey retrovirus fragments in Paul Offit’s RotaTeq vaccine.

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There are approximately 100 million allowable segments of DNA contamination permitted in any single vaccine dose. Much of this unwanted genetic and foreign protein rubbish has never been fully identified and sequenced. And vaccine makers are not required to identify what all of this genetic debris consists of. If a child follows the CDC’s recommended vaccination schedule from moments after birth until she or he reaches six years of age, 49 doses of 14 vaccines will have been administered. Isn’t it therefore time to pause and review the huge amount of DNA contamination, known and unknown viral genetic fragments children are receiving directly into their bloodstreams, and ask whether or not this may be contributing to the enormous rise in childhood autoimmune conditions, including common adult diseases now frequently appearing in children?

Dr. Howard Urnovitz is an immunologist trained at the University of Michigan and a leading advocate for informing scientists about vaccine-associated genetic mutations. He is perhaps best known for his research into genetic alterations among veterans suffering from Gulf War Syndrome. Although GWS has been associated with a wide range of toxic exposures, including chemical weapons, organophosphates, depleted uranium, an experimental anthrax vaccine, pesticides and other causes, Urnovitz’s discovery was singular. He identified genetic sequences in a particular chromosome well known as a “hot spot” for polymorphisms among many veterans. What was unusual was that the sequences were non-human and similar to the enteroviral segments from the oral polio vaccine administered to the veterans.

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Although this research cannot conclude that veteran’s GWS symptoms are directly related to the vaccine’s polio virus, it confirms the deep concern over viral genes introduced via vaccination jumping and recombining with our body’s DNA.

In light of the above discussions about gene jumping, recombination of pathogenic viral sequences merging with our bodies own DNA, undesirable mutations, and expression and activation of hereditary genetic predispositions leading to serious autoimmune complications and diseases, consider the following: Merck’s Rotateq vaccine for the protection of infants from rotavirus is a genetically engineered vaccine that includes five combined human and cow strains of rotavirus, first developed by Paul Offit at the Children’s Hospital of Pennsylvania. This viral concoction combines bovine rotavirus strains that causes diarrhea in cows with viral strains causing diarrhea in humans. This recombinant, engineered viral strain is then cultured on African Green Monkey kidney tissue. The seed stock that is later used to manufacture future lots of the vaccine also includes fetal bovine (cow) serum and porcine trypsin (an enzyme derived from a pig’s pancreas).

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Are we the only ones who share grave trepidations that an infant will receive a series of three rotavirus injections by the age of six months? And are we to believe that it is normal and safe for an infant to be unnaturally exposed to an artificial and abnormal pathogen in this manner?

The genetically engineered rotavirus vaccines, similar to many of the newer vaccines positioned to come on the market in the very near future, contain an attenuated live virus. These vaccines are already raising serious questions about their influential impact upon the vitality of the immune system, our bodies’ gut microbiome, and even environmental ecologies. In 2012, Norwegian scientists at the University of Tromsø concluded that “genetically engineered or modified viruses (GMVs) are being increasingly used as live vaccine vectors and their applications may have environmental implications…. In all cases there may be circumstances that enable GMVs to jump species barriers directly or following recombination with naturally occurring viruses.”

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Finally, the CDC aggressively follows a one-size-fits-all policy in its efforts to keep the entire American population vaccinated. Today there are over two hundred new vaccines in the pipeline and eventually coming to market. As new spikes in diseases occur consistently with each new vaccine approved and entered in the CDC’s recommended vaccination schedule, so also will other disease conditions increase as well as new disorders never observed before. People today are less healthy than previous generations. More and more people have compromised immune systems and are rapidly becoming immunodeficient. Surprisingly no federal agency or official institution tries to track the total number of people with serious compromised immune systems other than recipients of organ transplants, and people with cancer or positive HIV diagnoses. The American Autoimmune Related Diseases Associations estimates that 50 million people have any one of 100 and perhaps over 140 different life-threatening autoimmune diseases. Federal health officials downplay the severity of this epidemic by only counting 24 autoimmune diseases.

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In addition, poverty is on the rise and conservative estimates record 22% of all children living below the poverty level. Forty-eight million Americans live in insecure food households and are clinically malnourished whilst in the UK the figure is estimated at 10% of the population  This, too, is contributing to the increase in weakened immune systems and diseases. Other health disorders such as chronic lack of sleep, stress, and anxiety are now associated with weakened immunity and immunosuppressive disorders. All told, anywhere between 30-50 percent of UK People have weakened immune systems that make them far more susceptible to adverse complications due to vaccines. And live attenuated virus vaccines, which include measles, mumps, rubella, influenza, rotavirus, chickenpox, smallpox, and the live polio vaccine in foreign countries have been shown repeatedly to weaken natural immunity and make the recipient more predisposed to other viral infections.

It is essential that we accept that the science and technology to support vaccine safety remains in its infancy. For those vaccine developers who are looking at vaccination’s epigenetic effects on the human genome, our bodies’ microbiome, and the immune system, new and unexpected concerns over safety are coming to light. Moreover, no one is a greater expert on a child’s reaction to a vaccine than a parent. But most parents don’t have the scientific background to advocate for vaccine-induced injuries. Nor do the physicians, pediatricians, nurses, and pharmacists who oversee vaccination have the time and specialized medical training to fully understand each and every vaccine’s immunological and genetic complexities. Consequently, the official doctrine of vaccine safety is completely based upon blind belief and faith. Medical interventions imposed and mandated on the public should be based solely on scientific proof of safety, and the provaccine industry and federal authorities have never convincingly made their case based on gold standard scientific principles. Until the vaccine industry does so, no child’s or adult’s life should ever be put at unnecessary risk.

References

1. Habakus L, Holland M.Vaccine Epidemic.Skyhorse Press, New York 2012
2. Bruesewitz et al vs Wyeth LLC. //www.supremecourt.gov/opinions/10pdf/09-152.pdf
3. Shoenfeld Y, Agmon-Levin N.Vaccines and Autoimmunity.San Francisco: Wiley, 2015
4. Erickson N. France: Aluminum Adjuvants and HPV Vaccines Up for Debate. Sanevax.org. May 19, 2014.
5. Adhya D, Basu A. Epigenetic modulation of host: new insights into immune evasion by viruses.J Biosci. December 2010;35(4):647-663.

6. Fisher, BL. Emerging Risks of Live Virus and Virus Vectored Vaccines. National Vaccination Information Center. 2014.
7. Null, G.Silent Epidemic: The Untold Story of Vaccines(documentary film). 2013.
8. Buttram HE. The Ultimate Gamble: Do Childhood Vaccines Result in Genetic Hybridization from Alien Human and Animal DNA Contents? March 13, 2012.
9. Ho M-W, Cummins J. The vaccines are far more deadly than the swine flu. Institute of Science in Society. July 27, 2009.
10. Autistic genes are in all of us, new research reveals (press release). March 21, 2016. www.sciencedaily. com.
11. Autism and Schizophrenia: Scientists measure gene mutation rate. September 3, 2010.
12. //www.gardasilsyndrome.com
13. Shilhavy B. Are Vaccines Altering Our Genes Causing Brittle Bones in Infants? //vaccineimpact.com. 2015
14. Mayo Clinic. Decoding vaccination: Researchers reveal genetic underpinnings of response to measles vaccine (press release). September 23, 2011. https://www. sciencedaily.com
15. Gale R, Null G. Vaccines Dark Inferno: What is Not on Insert Labels. September 28, 2009. // blog.garynull.com/wp-content/uploads/2014/03/VaccinesDarkInferno2.pdf
16. Fisher BL. Vaccine Contamination: Pig Virus DNA Found in Rotarix. April 7, 2010.
17. Buttram H. Vaccines and Genetic Mutation. October 11, 2002. www.whale.to/a/yurko.html 18. Myhr AI, Traavik T. Genetically Engineered Virus Vectored Vaccines – Environmental Risk Assessment and Management Challenges. //cdn.intechopen. com/pdfs/25756.pdf 19. Schall T. How many Americans are immunocompromised.Bioethics Bulletin.February 11, 2015