Vaccine Contamination

Vaccine Contamination

Perhaps you may be one of the people that actually think that vaccines have been proven as safe and effective? So, you then as well have obviously believed that vaccines have been purified, regardless of what animal or human and now even insect substance and/or cell tissue the vaccine is grown on, or in. Its so all good, that it must be darn near to the equivalent of vaccine savior holy water, right? And would you believe as well that there is no known explanation for the chronic illness, disorders, and autoimmune conditions, and cancer; we are seeing an increasing amount of today, in all ages, but especially children?

Quite obviously this in not a only a problem with this type of vaccine, but it is a problem in all vaccines, regardless of the source of animal origin of the specific vaccine production. It has been a problem ever since it was known of SV 40 contamination in the early polio vaccine. It and this clearly continues to be a problem for all vaccines, based on other such contamination that has as well been noted in the literature and data. There is simply no known way by any current vaccine purification step process, to screen for all such potential contaminants. Even known contaminants can not all be screened out, much more unknown contaminants. The CDC has known this for decades, and they have admitted to the unknown risk to health. But you won’t read about that on the CDC site itself, but a subset of pages that was once available.

Biologicals

Evaluation of the Human Host Range of Bovine and Porcine Viruses that may Contaminate Bovine Serum and Porcine Trypsin Used in the Manufacture of Biological Products

Abstract
Current U.S. requirements for testing cell substrates used in production of human biological products for contamination with bovine and porcine viruses are U.S. Department of Agriculture (USDA) 9CFR tests for bovine serum or porcine trypsin. 9CFR requires testing of bovine serum for seven specific viruses in six families (immunofluorescence) and at least 2 additional families non-specifically (cytopathicity and hemadsorption). 9CFR testing of porcine trypsin is for porcine parvovirus. Recent contaminations suggest these tests may not be sufficient. Assay sensitivity was not the issue for these contaminations that were caused by viruses/virus families not represented in the 9CFR screen. A detailed literature search was undertaken to determine which viruses that infect cattle or swine or bovine or porcine cells in culture also have human host range [ability to infect humans or human cells in culture] and to predict their detection by the currently used 9CFR procedures. There are more viruses of potential risk to biological products manufactured using bovine or porcine raw materials than are likely to be detected by 9CFR testing procedures; even within families, not all members would necessarily be detected. Testing gaps and alternative methodologies should be evaluated to continue to ensure safe, high quality human biologicals.

Excerpts from the study:

“Current U.S. requirements for testing cell substrates used in production of human biological products (*VACCINES*) for contamination with bovine and porcine viruses are U.S. Department of Agriculture (USDA) 9CFR tests for bovine serum or porcine trypsin. 9CFR requires testing of bovine serum for seven specific viruses in six families (immunofluorescence) and at least 2 additional families non-specifically (cytopathicity and hemadsorption). 9CFR testing of porcine trypsin is for porcine parvovirus. Recent contaminations suggest these tests may not be sufficient. Assay sensitivity was not the issue for these contaminations that were caused by viruses/virus families not represented in the 9CFR screen. A detailed literature search was undertaken to determine which viruses that infect cattle or swine or bovine or porcine cells in culture also have human host range [ability to infect humans or human cells in culture] and to predict their detection by the currently used 9CFR procedures. There are more viruses of potential risk to biological products manufactured using bovine or porcine raw materials than are likely to be detected by 9CFR testing procedures; even within families, not all members would necessarily be detected….

Cell-culture derived vaccines for human use were developed in the 1950’s. Since fetal calf serum and bovine or porcine trypsin were used in cell culture, the 9CFR tests developed for veterinary use to screen for viruses that can infect cattle and swine were implemented by the authorities regulating human vaccines. However, many viruses not of significant concern to the cattle and swine industry are not addressed by the 9CFR testing. Today, over half a century after cell culture-derived vaccines were initially developed, the human biologics industry is still using the methods specified in the 9CFR regulations for testing FBS and porcine trypsin.”

Read more:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206158/

Plague: An Interview With Judy Mikovits
http://www.prohealth.com/library/showarticle.cfm?libid=18960&vote=finished#discuss

http://www.plaguethebook.com/

Not only aluminum from injected vaccine adjuvants is crossing the blood brain barrier due to polysorbate 80 in the vaccines, but as well now known other metals contamination in the vaccines.

Study: Almost All Vaccines Contaminated with Toxins and Linked to Side Effects
http://vaccineimpact.com/2017/study-almost-all-vaccines-contaminated-with-toxins-and-linked-to-side-effects/

New Quality-Control Investigations on Vaccines: Micro- and Nanocontamination
http://medcraveonline.com/IJVV/IJVV-04-00072.pdf

Part 1: Dirty Vaccines: Every Human Vaccine Tested Was Contaminated With Metals and Debris in New Study
http://www.greenmedinfo.com/blog/dirty-vaccines-every-human-vaccine-tested-was-contaminated-metals-and-debris-new-

Dirty Vaccines – Part Two: What the Industry Knows and Isn't Telling You
http://www.greenmedinfo.com/blog/dirty-vaccines-part-two-what-industry-knows-and-isnt-telling-you

Breaking Interview: Lead Author of 'Dirty Vaccines' Study Speaks Out
http://www.greenmedinfo.com/blog/breaking-interview-lead-author-dirty-vaccines-study-speaks-out

Polysorbate 80 in vaccines as well helps open the blood/brain barrier making it easier for toxic metals in vaccines and as well inflammation causing aluminum adjuvants to pass through.

Research Article
The Severity of Autism Is Associated with Toxic Metal Body Burden and Red Blood Cell Glutathione Levels

Abstract

This study investigated the relationship of children's autism symptoms with their toxic metal body burden and red blood cell (RBC) glutathione levels. In children ages 3–8 years, the severity of autism was assessed using four tools: ADOS, PDD-BI, ATEC, and SAS. Toxic metal body burden was assessed by measuring urinary excretion of toxic metals, both before and after oral dimercaptosuccinic acid (DMSA). Multiple positive correlations were found between the severity of autism and the urinary excretion of toxic metals. Variations in the severity of autism measurements could be explained, in part, by regression analyses of urinary excretion of toxic metals before and after DMSA and the level of RBC glutathione (adjusted of 0.22–0.45, in all cases). This study demonstrates a significant positive association between the severity of autism and the relative body burden of toxic metals.

http://www.hindawi.com/journals/jt/2009/532640/ (full study)

Metals Debris Found in Vaccine Supply
http://www.ecowatch.com/kennedy-metal-debris-vaccines-2276687112.html

New Quality-Control Investigations on Vaccines: Microand
Nanocontamination
http://medcraveonline.com/IJVV/IJVV-04-00072.pdf

Lead, Iron, Chromium and Other Metals Routinely Contaminate Vaccine Adjuvants, Industry Study Reports
http://info.cmsri.org/aluminum-and-your-health-blog/lead-iron-chromium-and-other-metals-routinely-contaminate-vaccine-adjuvants-industry-study-reports?utm_campaign=eBook%3A+Age+of+Aluminum&utm_content=46490849&utm_medium=social&utm_source=facebook

The Impact of Toxins on the Developing Brain
Annual Review of Public Health

Abstract

The impact of toxins on the developing brain is usually subtle for an individual child, but the damage can be substantial at the population level. Numerous challenges must be addressed to definitively test the impact of toxins on brain development in children: We must quantify exposure using a biologic marker or pollutant; account for an ever-expanding set of potential confounders; identify critical windows of vulnerability; and repeatedly examine the association of biologic markers of toxins with intellectual abilities, behaviors, and brain function in distinct cohorts. Despite these challenges, numerous toxins have been implicated in the development of intellectual deficits and mental disorders in children. Yet, too little has been done to protect children from these ubiquitous but insidious toxins. The objective of this review is to provide an overview on the population impact of toxins on the developing brain and describe implications for public health.

http://www.annualreviews.org/doi/full/10.1146/annurev-publhealth-031912-114413

A direct response to the article titled: I love it when an antivax “study” meant to show how “dirty” vaccines are backfires so spectacularly - Posted by Orac (Gorski) on February 2, 2017
http://www.vacfacts.info/a-direct-response-to-the-article-titled-i-love-it-when-an-antivax-study-meant-to-show-how-dirty-vaccines-are-backfires-so-spectacularly.html

Autism Spectrum Disorders and Aluminum Vaccine Adjuvants
Lucija Tomljenovic, Russell L. Blaylock, Christopher A. Shaw

Abstract
Impaired brain function, excessive inflammation, and autoimmune manifestations are common in autism. Aluminum (Al), the most commonly used vaccine adjuvant, is a demonstrated neurotoxin and a strong immune stimulator. Hence, adjuvant Al has the necessary properties to induce neuroimmune disorders. Because peripheral immune stimuli in the postnatal period can compromise brain development and cause permanent neurological impairments, the possibility that such outcomes could also occur with administration of Al vaccine adjuvants needs to be considered. In regard to the risk of adjuvant toxicity in children, the following should be noted: (i) children should not be viewed as “small adults” as their unique physiology makes them more vulnerable to toxic insults; (ii) in adult humans Al adjuvants can cause a variety of serious autoimmune and inflammatory conditions including those affecting the brain, yet children are routinely exposed to much higher amounts of Al from vaccines than adults; (iii) compelling evidence has underscored the tight connection between the development of the immune system and that of the brain. Thus, it appears plausible that disruptions of critical events in immune development may also play a role in the establishment of neurobehavioral disorders; (iv) the same immune system components that play key roles in brain development appear to be targeted for impairment by Al adjuvants. In summary, research data suggests that vaccines containing Al may be a contributing etiological factor in the increasing incidence of autism.

http://link.springer.com/referenceworkentry/10.1007%2F978-1-4614-4788-7_89

And what do multiple vaccines combined with aluminum adjuvants do? They over-activate the brains microglia cells and with resulting long term levels of brain inflammation. The studies and the data are all there on the page that I gave you

Journal of American Nutraceutical Association 6: 21-35, 2003.
Interaction of Cytokines, Excitotoxins, and Reactive Nitrogen and Oxygen Species in Autism Spectrum Disorders, Russell Blaylock, MD* Medical Director, Advanced Nutritional Concepts Ridgeland, Mississippi

ABSTRACT

There is growing and compelling evidence that excessive peripheral as well as central immune activation of brain microglia can result in alterations in brain growth and connectivity during rapid brain growth, the so-called "brain growth spurt." A considerable amount of evidence, presented in this paper, demonstrates the deleterious effects of immune factors, such as cytokines, chemokines, and excitotoxins, when present in excess. The interaction between excitotoxicity, ROS and RNS injury and immune dysfunction is discussed. It is concluded that excessive activation of the brain's immune system during critical growth periods can occur when vaccines are given as combination vaccines, using schedules that are too close together or by the use of certain live viruses in the vaccines.

http://www.nutrimedical.com/news.jhtml?method=view&news.id=1084

Vaccines Will be Made from Human Cancer Tumors
https://vactruth.com/.../vaccines-made-from-cancer-tumors/

Dr. Deisher testifies on the connection between vaccines and rising rates of autism (1 of 4).

Published on Dec 5, 2012
Dr. Deisher testifies at the MN House about vaccine safety. She presents research demonstrating a link between the rise in the rates of autism and the use of aborted fetal cells in the production of vaccines. Dr. Deisher is the president and founder of SoundChoice, a non-profit that works to provide safe vaccination alternatives.

https://www.youtube.com/watch?v=ZsCAUKUTb20

Dr. Deisher testifies on the connection between vaccines and rising rates of autism (2 of 4).
https://www.youtube.com/watch?v=I5b9xsGZs1E

Dr. Deisher testifies on the connection between vaccines and rising rates of autism (3 of 4).
https://www.youtube.com/watch?v=-UVZSs9vgYQ

Dr. Deisher testifies on the connection between vaccines and rising rates of autism (4 of 4).
https://www.youtube.com/watch?v=M5y9mYQQmt4

Dr. Theresa Deisher: Moral Vaccine Development
https://www.youtube.com/watch?v=BTEh_BsGwZQ

Autism

The dangers of using aborted fetal cell lines for vaccine manufacture have been debated by the FDA for over 50 years, and yet they have not done sufficient safety studies. The active component of a vaccine is a virus. Viruses are too large to manufacture in test tubes. Therefore, vaccine manufacturers exploit the natural method of producing virus– they inoculate cells and the cells produce the virus for them. Each vial of vaccine contains contaminants from the cells used to make the virus. When we use animal cells to make viruses, the residual material is not human and so we mount an immune response to it and eliminate it. However, in the case of vaccines produced using aborted human fetal cell lines, we have the dangers of triggering an autoimmune response and insertion of the contaminating DNA to disrupt the child’s own genes.

In the US, autism has spiked up in 3 distinct years, called changepoints. The first changepoint occurred in 1981, the second in 19881, and the third in 1996. These spikes coincide with the introduction of vaccines that are produced in aborted fetal cells. In 1979, aborted fetal cell produced MMR II was approved in the US. Compliance campaigns brought MMR II use up from as low as 49% for children born before 1987 to over 82% for children born in 1989 and later. A second dose of MMR II was also introduced to the vaccination schedule for children born in 1988 and later. The third changepoint corresponds to the approval of aborted fetal cell produced Varivax (chickenpox) in 1995 (See figure below).

Read more: http://soundchoice.org/autism/

Pay particular attention to as well the below related study.
June 3, 2010
SCPI Study on Aborted Fetal DNA in Vaccines Presented at International Meeting for Autism Research

http://www.cogforlife.org/scpiautismstudypress.htm

http://www.cogforlife.org/scpiautisminsarabstract.htm

For Scientific Data: Homologous Recombination Study
http://www.cogforlife.org/SCPIIMFARHR.pdf

Vaccine Production With - Human Diploid Cells (aborted fetal cell tissue)
http://www.vacfacts.info/vaccine-production-with---human-diploid-cells-aborted-fetal-cell---tissue.html

Vaccine Truth Informational - Brochures:

Do not allow all of the vaccine-injured childrens injuries to be in vain. Educate others in honor of them. Be the Voice for those who don't have one. Do not be silent. You can inform other parents. We provide multiple free brochures you can give to educate other parents.

Download and print them now.
http://www.educate4theinjured.org/eric/4571993523

Scientific proof that the known cancer causing SV40 virus, a previous contaminant in the polio vaccine, is obviously either contagious; or the virus is still in the vaccine/s.
http://www.vacfacts.info/scientific-proof-that-the-known-cancer-causing-sv40-virus-a-previous-contaminant-in-the-polio-vaccine-is-obviously-either-contagious-or-the-virus-is-still-in-the-vaccines.html

Millions of Children Infected with 'Vaccine Safety Experts' Rotateq Vaccine: Dr. Paul Offit

Unfortunately for Dr. Offit (not so affectionately named Dr. Profit), a 2010 study published in Journal of Virology revealed that his multi-million dollar grossing patent on the Rotateq vaccine contains a live simian retrovirus (with a 96% match of certainty) that has likely infected millions of children over the past few years with a virus that causes great harm. Retrovirus infections are permanent, and can carry on indefinitely into future generations. In other words, once they are inserted into the human genome they can not be removed. View the entire PDF here.

Moreover, a 2014 study published in Advances in Virology found Dr. Offit's vaccine contains a "a baboon endogenous virus strain M7...likely due to the monkey cell line in which RotaTeq was produced from." View the entire PDF here.

Read more:
http://www.greenmedinfo.com/blog/breaking-news-millions-children-infected-vaccine-safety-experts-rotateq-vaccine

Rotavirus Vaccines Still Contaminated With Pig Virus DNA
http://www.greenmedinfo.com/blog/rotavirus-vaccines-still-contamined-pig-virus-dna

Vaccine Contamination: Pig Virus DNA Found in Rotarix
http://www.nvic.org/nvic-vaccine-news/april-2010/vaccine-contamination-pig-virus-dna-found-in-rota.aspx

VACCINE CONTAMINATION: A THREAT TO HUMAN HEALTH
http://www.nvic.org/Downloads/Rotavirus-Campaign/VACCINE-CONTAMINATION--A-THREAT-TO-HUMAN-HEALTH.aspx

Vaccine Contamination Pig Virus DNA Found in Rotarix April 7, 2010
http://www.youtube.com/watch?v=Jf26A14pX58

The Emerging Risks of Live Virus & Virus Vectored Vaccines:
Vaccine Strain Virus Infection, Shedding & Transmission
http://www.nvic.org/CMSTemplates/NVIC/pdf/Live-Virus-Vaccines-and-Vaccine-Shedding.pdf

Pig Virus DNA Found in Rotavirus Vaccine
FDA: No Problems Seen in 1 Million U.S. Kids Who Got Rotarix Vaccine, (how would they know, they have never studied it nor do they even know what to look for.
http://www.webmd.com/children/vaccines/news/20100322/pig-virus-found-in-gsk-rotavirus-vaccine

SANE Vax Inc. Discovers Potential Biohazard Contaminant in Merck's Gardasil™ HPV 4 Vaccine
http://www.youtube.com/watch?v=qcGz-Pl_SGA

SANE Vax to FDA: Recombinant HPV DNA found in multiple samples of Gardasil
http://sanevax.org/sane-vax-to-fda-recombinant-hpv-dna-found-in-multiple-samples-of-gardasil/

FDA Reply Letter - and Further Questions Raised on Gardasil
http://www.vacfacts.info/fda-reply-letter---and-further-questions-raised-on-gardasil.html

Again, the major issue with Gardasil, the finding of the presents in the vaccine, of vaccine strain HPV-DNA, attached to the aluminum adjuvant. This is a huge issue and the FDA has done nothing but deny and down play it, it is an issue that would force a spotlight on all vaccines and they know it. It forces open a swell the whole issue of what is known as molecular mimicry, in regard to the harm of vaccines. The CDC will as well dodge these issues until hell freezes over, if they can. There are similar contamination issues and have been noted and written on, with, Rotarix, Gardasil, and as well the MMR vaccine. MMR vaccine also uses human diploid tissue, in its production. The CDC is asleep that the science board room, on all levels; intentionally. The incoming science has literally and apparently very little of it made its way to their desks since 1961, when the crank telephones were replaced with the ones with rotary dials. Apparently they thought they had enough information. That's right, I made that part up, but in a literal sense, it is all to near to frighteningly true.

The persistence of HPV DNA fragments and adverse effects in HPV shot recipients
http://www.examiner.com/article/the-persistence-of-hpv-dna-fragments-and-adverse-effects-hpv-shot-recipients

The Experts admitted Ignorance
http://albamora.com/joanmorahomeopatia/pdf/Aluminum%20in%20Vaccines%20-from%20forthcoming%20book.pdf

HPV and HPV Vaccine - Facts and Truth
http://hpvfacts.co.uk/

Death after Quadrivalent Human Papillomavirus (HPV) Vaccination: Causal or Coincidental?

Conclusions: Our study suggests that HPV vaccines containing HPV-16L1 antigens pose an inherent risk for
triggering potentially fatal autoimmune vasculopathies.

http://www.rescuepost.com/files/ltshaw-death-after-quadrivalent-hpv-vaccination-pharma-reg-affairs-2012.pdf

Gardasil Destroys Girl’s Ovaries: It Should Have Been Predicted
http://gaia-health.com/gaia-blog/2012-10-18/gardasil-destroys-girls-ovaries-it-should-have-been-predicted/

Two sisters, 20 and 19, are suing the makers of the HPV vaccine, claiming the drug caused them to lose their fertility
Madelyne (20) and Olivia (19) Meylor have filed a lawsuit against the makers of the HPV vaccine, blaming it for their premature infertility
http://www.dailymail.co.uk/news/article-2491874/Two-sisters-20-19-suing-makers-HPV-vaccine-claiming-drug-caused-lose-fertility.html

Gardasil Destroys Girl’s Ovaries: Research on Ovaries Never Considered
http://gaia-health.com/gaia-blog/2012-10-17/gardasil-destroys-girls-ovaries-research-on-ovaries-never-considered/

Teenage Girl Becomes Infertile after Gardasil Vaccination
http://pop.org/content/teenage-girl-becomes-infertile-after-gardasil-vaccination

The Coming Push to Give HPV Vaccines to Infants
http://gaia-health.com/gaia-blog/2013-08-01/the-coming-push-to-give-hpv-vaccines-to-infant-people/

Vaccines Can Cause Infertility
http://vactruth.com/2013/07/20/vaccines-can-cause-infertility/

Cervarix Just as Dangerous as Gardasil
http://naturalsociety.com/merck-gardasil-cervarix-dangerous/

Gardasil Vaccine Found to be Contaminated
http://sanevax.org/gardasil-vaccine-found-to-be-contaminated/

http://sanevax.org/

Gardasil Vaccine rDNA Introduced at Coroner’s Inquest
http://vactruth.com/2012/08/09/gardasil-rdna-coroners-inquest/

Bombshell Interview Reveals DNA Fragments Discovered 6 Months After Vaccination, (Gardasil)
http://vactruth.com/2012/08/16/rdna-fragments-after-vaccination/

Gardasil: New Study Brings More Safety Questions to Light

By Norma Erickson, President

Excerpts:

Why were HPV-16 L1 DNA fragments detected in post mortem samples taken six months after Gardasil vaccination and not the other vaccine-relevant types? Dr. Sin Hang Lee, of Milford Hospital and Milford Molecular Laboratory, may have provided an answer in his most recently published paper entitled, Topological conformational changes of human papillomavirus (HPV) DNA bound to an insoluble aluminum salt – A study by low temperature PCR.[1] His findings suggest that non-B-conformational changes in HPV L1 gene DNA fragments bound to the AAHS adjuvant may be genotype related, in other words specific to HPV-16.

In September 2011, SaneVax Inc. informed the FDA that despite all claims stating Gardasil contained ‘no viral DNA’ Dr. Lee had discovered there were indeed fragments of HPV-11, HPV-16 and HPV-18 L1 DNA firmly attached to Merck’s proprietary aluminum adjuvant in 100% of the samples he tested, but all were lacking a region amplifiable by an MY09 degenerate primer.[2] The FDA was quick to confirm that Gardasil does contain residual HPV L1 gene DNA fragments,[3] but that these fragments posed no health risk. The FDA completely ignored a request for further investigations put forth by the SaneVax Team.[4]

In light of the FDA statement corroborating Dr. Lee’s previous findings, the presence of HPV DNA fragments of vaccine origin in the bodies of recipients might be anticipated after intramuscular injections of Gardasil. However, finding HPV-16 L1 DNA fragments in post-mortem blood samples of a teenager who died six months after completion of 3 Gardasil injections without finding any other vaccine-relevant fragments was a surprise.[5] Obviously, further investigations were necessary.

At the request of SaneVax Inc., Dr. Lee agreed to use PCR amplification followed by direct DNA sequencing to try and determine what was going on. What he discovered is stated clearly in the conclusion of the above referenced paper. It says:

Where does this leave the average medical consumer? Unfortunately, it leaves them with the following unanswered questions:

Once injected, how long will the HPV-16 L1 DNA fragments attached to aluminum remain in my body?

Are the non-B conformation HPV fragments in Gardasil potentially harmful?

Will the non-B conformation DNA fragments in Gardasil induce autoimmune disorders?

Will the non-B conformation DNA get integrated in the genome causing mutagenesis and/or cancer?

The scientific community needs to investigate these potential risks immediately. Medical consumers need to know the risks as well as any potential benefits before they decide if Gardasil is right for them.

In the interest of public health and safety, the FDA needs to rescind approval for Gardasil until satisfactory answers are provided to the four questions above. The time for poke and hope is long since passed. Medical consumers need proof this vaccine is safe.

Read more:
http://sanevax.org/gardasil-new-study-brings-more-safety-questions-to-light/

Roxy Fiste, Mother of Brittany Fiste, interview detailing what happened to her daughter Brittany, after Gardasil. Listen to the account of the doctors denial of all; no matter how bad it was.
http://www.youtube.com/watch?feature=player_embedded&v=-zAo_ewCtWI

HEALTH ALERT: Gardasil Victim Speaks Out After 2 Years

Brittney Fiste, gives an emotionally charged overview of what her life has been like for the past two years. She struggles daily with the fact her life has been forever changed. A doctor frightened her into taking the Gardasil vaccine by telling her she could get HPV through a “possible” lab accident at college – where her blood could mingle with someone else’s who had HPV. She was never told HPV is a sexually transmitted disease and having no other information, she allowed herself to be given a vaccine she never needed. Now she wishes the TRUTH to be told.

http://www.youtube.com/watch?feature=player_embedded&v=0gCVCP8BFrU

Truth About Gardasil, (personal accounts of the harm done)
http://truthaboutgardasil.org/

HPV vaccine (Gardasil) – Seizures, Fainting, Paralyis, ….(Updated Chart)
(Endless more personal accounts of the HPV vaccine harm)
http://www.kkrasnowwaterman.com/blog/tabid/2962/bid/5747/HPV-vaccine-Gardasil-Seizures-Fainting-Paralyis-Updated-Chart.aspx

Judicial Watch Seeks Answers to Payouts Made to Victims of HPV Vaccines
http://www.thelibertybeacon.com/2013/03/16/judicial-watch-seeks-answers-to-payouts-made-to-victims-of-hpv-vaccines/

FEDS SUED FOR SECRETS ON HPV VACCINE DEATHS
Other reported injuries include seizures, paralysis, blindness, memory loss
http://www.wnd.com/2013/03/feds-sued-for-secrets-on-hpv-vaccine-deaths/

FOIA Documents Obtained by Judicial Watch Reveal 200 Claims Filed With HHS for HPV Vaccine Injuries and Deaths, 49 Compensated
http://finance.yahoo.com/news/foia-documents-obtained-judicial-watch-181118192.html

PRESS RELEASE

March 20, 2013, 2:12 p.m. EDT

FOIA Documents Obtained by Judicial Watch Reveal 200 Claims Filed With HHS for HPV Vaccine Injuries and Deaths, 49 Compensated

Documents Reveal That the National Vaccine Injury Compensation Program (VICP) Has Paid Out Nearly $6 Million in Claims to Victims of Controversial HPV (Human Papillomavirus) Vaccine, Including Families of Two Dead

http://www.marketwatch.com/story/foia-documents-obtained-by-judicial-watch-reveal-200-claims-filed-with-hhs-for-hpv-vaccine-injuries-and-deaths-49-compensated-2013-03-20

HPV VACCINE VAERS REPORTS UP TO FEB 2013

Description                                         Total
Disabled                                              927
Deaths                                  130
Did Not Recover                                               5,791
Abnormal Pap Smear                                     518
Cervical Dysplasia                                             206
Cervical Cancer                                 62
Life Threatening                                               546
Emergency Room                                            10,261
Hospitalized                                       2,917
Extended Hospital Stay                                 227
Serious                                 3,914

Adverse Events                                                29,003

http://sanevax.org/

And, this is well known to represent a reporting factor of only 1 to 10% of the total adverse reactions. Do the math?

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF COLUMBIA, (they clearly as well did NOT exactly volunteer this payout information)

Plaintiff Judicial Watch, Inc. brings this action against Defendant U.S. Department of Health & Human Services to compel compliance with the Freedom of Information Act, 5 U.S.C. §

552 (“FOIA”). As grounds therefor, Plaintiff alleges as follows:

Read more:
http://www.scribd.com/doc/127829695/Gardasil-Complaint-2-28-2013

Gardasil Scientific References and Citations, (regarding harm)
http://www.educate4theinjured.org/#/gardasil-studies/4567298238

Educate For The Vaccine Injured
http://www.educate4theinjured.org/

Aluminum Adjuvants - Lack of Safety Data - Lack of Aluminum Adjuvant Safety Studies
http://www.vacfacts.info/aluminum-vaccine-adjuvants.html

The Vaccine Damage Science
http://www.vacfacts.info/the-vaccine-damage---science.html

30 Stunning Facts They Don’t Want You to Know about Gardasil and HPV Vaccines
http://www.sovereignindependentuk.co.uk/2012/09/11/30-stunning-facts-they-dont-want-you-to-know-about-gardasil-and-hpv-vaccines/

Merck Now Bribing College Girls to Complete Gardasil Vaccine
http://healthimpactnews.com/2013/merck-now-bribing-college-girls-to-complete-gardasil-vaccine/

HPV Vaccines: Scientists Use Manufacturers’ Data to Prove Lack of Efficacy
http://gaia-health.com/gaia-blog/2012-10-28/hpv-vaccines-scientists-use-manufacturers-data-to-prove-lack-of-efficacy/

Australian boys become first male guinea pigs in global Gardasil genocide, (what a tragedy)
http://www.naturalnews.com/039279_Gardasil_guinea_pigs_Australia.html

CDC Now Pushes Gardasil HPV Shot on All Boys 11 to 12
http://naturalsociety.com/cdc-now-pushes-gardasil-hpv-shot-on-all-boys-11-to-12/

Boys to get free Gardasil vaccine

Excerpts:

A vaccine developed in Queensland has been given to young girls since 2007. Ever since, there have calls to broaden the scheme to include boys.

Federal Health Minister Tanya Plibersek says boys aged 12 and 13 will now be given three doses of the Gardasil vaccine under the National Immunisation Program.

"This is a very important next step in the story of Gardasil," she said.

"It's a very exciting journey, an Australian invention, a world-first vaccine for women and now a world-first vaccine for young men."

Ms Plibersek says year 9 boys will also be able to get the vaccine at school under a catch-up program for the next two years.

The vaccination program for boys is expected to cost $21.1 million over four years.

Read more:
http://www.abc.net.au/news/2012-07-12/hpv-vaccine-extended-to-boys/4126354

Deep sequencing reveals viral vaccine contaminants
http://www.virology.ws/2010/03/29/deep-sequencing-reveals-viral-vaccine-contaminants/

Unveiling the Culprit – Is Foreign DNA Contamination the Autistic Villain behind Biologic Vaccine Injuries?
http://holyhormones.com/womens-health/cancer-womens-health/cervical-cancer/unveiling-the-culprit-is-foreign-dna-contamination-the-autistic-villain-behind-biologic-vaccine-injuries/

Autism Epidemic, Is Foreign DNA in MMR II Vaccine Responsible? CBCD Suggests CDC Study Microcompetition Theory
The Center for the Biology of Chronic Disease (CBCD) believes that the cause of the epidemic is the foreign DNA in the MMR II vaccine.
http://www.prweb.com/releases/2012/4/prweb9359508.htm

Toxic Vaccines? CBCD Sends Letter to FDA & CDC on Foreign DNA Fragments in Gardasil and MMR
The CBCD sent a letter this past week to the offices of the FDA Commissioner, Dr. Margaret Hamburg,and to the offices of the CDC’s director, Dr. Thomas R. Frieden.
http://www.prweb.com/releases/2012/9/prweb9924299.htm

Do you think they know, at the FDA? Oh yes, they definitely know. What are they doing? Nothing. They are simply, they and the CDC, white washing it all and when they are forced to answer to any of this.

Emerging Infectious Diseases, Adventitious Agents and Vaccines
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2631857/pdf/11485673.pdf

SANE Vax Inc. Discovers Potential Bio-hazard Contaminant in Merck’s Gardasil HPV 4 Vaccine
http://holyhormones.com/womens-health/cancer-womens-health/cervical-cancer/sane-vax-inc-discovers-potential-bio-hazard-contaminant-mercks-gardasil-hpv-4-vaccine/

Gardasil® HPV DNA Discovered in Post-Mortem Blood and Spleen Tissue
http://www.businesswire.com/news/home/20120808006480/en

This below study actually does anything but, reassure the non contaminant safety of vaccines; and as well yet leaves many unknowns.

Viral Nucleic Acids in Live-Attenuated Vaccines: Detection of Minority Variants and an Adventitious Virus
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2876658/

Biohazard potential for live viral vaccines containing naked or free nucleic acids from contaminating (adventitious) viruses.

Excerpt: The hazards of horizontal gene transfer

Horizontal gene transfer (HGT) refers to the direct uptake and incorporation of genetic material from unrelated species, in this instance from adventitious viral contaminants in live viral vaccines into a human host or a host-related bacteria such as those colonizing the gut. HGT is uncontrollable. Unlike chemical pollutants which break down and become diluted out, nucleic acids are infectious, they can invade cells and genomes, to multiply, mutate and recombine indefinitely.

Potential hazards of HGT of naked/free nucleic acids include:

•   Generation of new viruses that cause disease

•   Generation of new bacteria that cause diseases

•   Spreading drug and antibiotic resistance genes among the viral and bacterial pathogens, making infections untreatable

•    Random insertion into genomes of cells resulting in harmful effects including cancer

•    Reactivation of dormant viruses, present in all cells and genomes, which may cause diseases

•    Multiplication of ecological impacts due to all the above

It is relevant to the issue of regulatory oversight that while the technology to detect these adventitious agents and their “cryptic” consequences was not available until relatively recently, both the dangers of generating new viruses and bacteria that can cause diseases, and spreading drug and antibiotic resistance among the pathogens, were foreseen by the pioneers of genetic engineering. That was why they called for a moratorium in the Asilomar Declaration of 1975. But commercial pressures cut the moratorium short, and guidelines were set up based on assumptions, every one of which has been invalidated by scientific findings since .

The presence of dormant and relict viral sequences in the human and other animal genomes has been known for at least 20 years . These include human retroviral sequences that have been identified in live viral vaccines grown in human cells. In addition Victoria et al1 have confirmed the presence of viral particle-associated avian leucosis virus in the MMR vaccine. The combination of three RNA viruses with the enzymatic machinery to convert RNA into complementary DNA (cDNA) that is then capable of causing all the aforementioned problems with naked/free DNA, presents a particularly worrying biohazard. Not only are endogenous viruses such as HRV able to exert this effect on RNA vaccine viruses, as shown by Klennerman and Zinkernagel for lymphocytic choriomeningitis virus (LCMV) , but also viral transgenes have been found to recombine with defective viruses such as HRV, to generate infectious recombinants . In turn, recombination between exogenous and endogenous viral sequences are associated with animal cancers .

PCV Type 2: presence and pathogenesis

PCV Type 2 is a lymphotropic virus that infects primary lymphoid tissues . Its detection in exposed (vaccinated) children should be focused on these tissues. They are available in intestinal biopsies from children with a variety of conditions including autism. They are also available from rhesus macaques exposed to the current vaccine schedule as part of ongoing

Read more: http://www.coalitionforvaccinesafety.org/docs/Biohazard_vaccines%20contaminant-CVS.doc

Latent infection and abnormal cell proliferation
By Hanan Polansky, November 7, 2002
http://www.cbcd.net/microcompetition.pdf

A CLEAR ISSUE OF VACCINE CONTAMINATION, Gardasil. If any doctor could and would, after hearing this below audio information, still offer the Gardasil vaccine to any person whatsoever; you are clearly conducting an irresponsible and CRIMINAL act, and offense!!! Wake up!

The Gary Null Show – Special on Safety and Efficacy of Vaccines, Specifically Gardasil – 03/22/13
http://prn.fm/2013/03/22/the-gary-null-show-special-on-safety-and-efficacy-of-vaccines-specifically-gardasil-032213/#axzz2OHB4UTFx

Audio conference link, Gary Null
<iframe width="250" height="24" src="http://prn.fm/?powerpress_embed=102421-podcast&powerpress_player=default" frameborder="0" scrolling="no"></iframe>

Chickenpox Vaccine Use is Highly Statistically Related to Autism Disorder; (using by the way, human diploid tissue in manufacture)
http://onemoresoul.com/news-commentary/chickenpox-vaccine-use-is-highly-statistically-related-to-autism-disorder.html

Varicella and Shingles Vaccine - For Profit Quackery
http://www.vacfacts.info/varicella-and-shingles-vaccine---for-profit-quackery.html

Vaccines don't shed? That is what they tell us; right? Your sure? Take a look. And they state that it is the vaccinated that are at risk from the un-vaccinated? Really? It looks to be exactly the other way around, to me?

Post Vaccination - Vaccine Targeted Strain - Viral and Bacterial Pathogen - Shedding
http://www.vacfacts.info/post-vaccination-vaccine-targeted-strain---viral-and-bacterial---shedding.html

Foreign DNA Fragments Cause Most Major Diseases, Dr. Hanan Polansky

Excerpt:

In the nucleus, "microcompetition" between the foreign N-boxes and the human N-boxes in the human genes can lead to a major disease. When the foreign N-boxes belong to a virus, microcompetition between the viral DNA and the human DNA can lead to disease even when the virus is latent (dormant), or the viral DNA is broken into pieces and cannot express proteins. As predicted by Dr. Hanan Polansky, many studies found fragments of DNA that belong to these viruses in tumors, clogged arteries (arterial plaque), arthritic joints, and other diseased tissues.

Read More:

http://www.cbcd.net/index.php

Gardasil: Dr. Hanan Polansky Explains How the Foreign DNA Fragments Found in the Vaccine can Cause Disease

The FDA asserts that the foreign DNA fragments found in Gardasil pose no risk. In contrast, Dr. Hanan Polansky, from the Center for the Biology of Chronic Disease, uses his highly acclaimed discovery of Microcompetition to explain how these DNA fragments can cause major diseases.

Read more:
http://www.prweb.com/releases/2012/2/prweb9162053.htm

http://viralsepidemic.com/vaccines/dr-hanan-polansky-explains-how-the-foreign-dna-fragment-found-in-vaccine-can-cause-disease/#more-182

Here is of course the FDA's WHITE wash denial and in denial of all, spin on it!

FDA Information on Gardasil – Presence of DNA Fragments Expected, No Safety Risk,

(Nothing is EVER enough, and nothing ever will be, as they know they have simply to much to lose if the truth be admitted to. Actually think about the magnitude of that liability. And thus it continues unabated. Currently they have no liability risk for anything as none of them can be sued due to the federal court being the current entity to cover that in a and the no fault so to speak fashion that they do through the National Vaccine Injury Compensation Program. However, if it were EVER admitted to that vaccines have done what they have, on a complete break down of this vaccine program under the spotlight it deserves; the NVIP, the compensation fund fees on vaccines, and taxpayers would never be able to bail them out of it nor that kind of implied liability. Nor would it prevent the loss of all their believed authoritative credibility, and possibly many careers. They obviously would and do realize that fact.

http://www.fda.gov/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm276859.htm

Now, let’s go to some more actual truth and reality.

Foreign DNA Fragments Found In Vaccines Can Cause Disease

Excerpts:

The FDA asserts that the foreign DNA fragments found in Gardasil pose no risk. In contrast, Dr. Hanan Polansky, from the Center for the Biology of Chronic Disease, uses his highly acclaimed discovery of Microcompetition to explain how these DNA fragments can cause major diseases.

Gardasil is the FDA approved HPV vaccine. As of September 15, 2011, the Centers for Disease Control (CDC) received a total of 20,096 reports of adverse events in relation to Gardasil vaccination. Dr. Hanan Polansky, Director of the Center for the Biology of Chronic Disease, will discuss his discovery of Microcompetition with Norma Erickson, President of SANE Vax Inc. Dr. Polansky will use Microcompetition to explain the biological mechanism underlying the Gardasil adverse events.

Dr. Hanan Polansky discovered that fragments of DNA, called N-boxes, can be very dangerous. When foreign N-boxes enter the body (naturally, or artificially, like through an injection of some treatment), they end up in the nucleus, where they attract scarce genetic resources. It is interesting that many common dormant (latent) viruses have strong N-boxes in their DNA. They include the Epstein-Barr virus (EBV), Cytomegalovirus (CMV), Herpes Simplex virus (HSV), Varicella Zoster virus (VZV), Hepatitis B Virus (HBV), Hepatitis C Virus (HCV), Human Papillomavirus (HPV), and others. In fact, the CMV virus has the strongest N-box known to science. This N-box is so strong that human genes cannot compete with its power to attract the scarce genetic resources.

View the video: (The information credits for this video are as well listed on the video page itself).
http://www.youtube.com/watch?v=FUa19tLdwhs

The Internet Journal of Infectious Diseases ISSN: 1528-8366
Book Review: Microcompetition with Foreign DNA and the Origin of Chronic Disease

Excerpt:

I work in the field of gene therapy, in which up to now, the most efficient gene delivery vehicles have been of viral origin, with retrovirus and adenovirus-based vectors being the most dominant players. In the minds of people concerned about the safety of these approaches, insertional mutagenesis into the host genome by retroviruses and acute immune reactions to adenoviruses rank on the top of the list. I have yet seen anyone in the field who realizes that the introduced foreign DNA associated with the delivery vector may have a profound impact on human health through microcompetition for host transcriptional factors. The major impact of this book on many specialties including gene therapy will be felt strongly in the coming years.

Liqun Zhang PhD

Research Associate, Cystic Fibrosis/Pulmonary Research and Treatment Center, University of North Carolina

Chapel Hill

Citation: L. Zhang: Book Review:

Microcompetition with Foreign DNA and the Origin of Chronic Disease. The Internet Journal of Infectious Diseases. 2004 Volume 3 Number 2. DOI: 10.5580/197b

The said review, (one professional to the other)
http://www.ispub.com/journal/the-internet-journal-of-infectious-diseases/volume-3-number-2/book-review-microcompetition-with-foreign-dna-and-the-origin-of-chronic-disease.html#sthash.ODEbfEHG.dpbs

Book by Hanan Polansky: Microcompetition with Foreign DNA and the Origin of Chronic Disease (Purple Book)

http://www.cbcd.net/Book.php

http://www.cbcd.net/index.php

http://www.cbcd.net/Book%20by%20Hanan%20Polansky%20(Purple%20Book).pdf

Microcompetition with foreign DNA and the Origin of Chronic Disease. [Paperback]

On Theory

A selection from: Microcompetition with Foreign DNA and the Origin of Chronic Disease

by Hanan Polansky, August 2004

Read more:
http://www.cbcd.net/Hanan%20Polansky%20on%20Theory.pdf

Radio interview with Dr. Polansky on February 4, 2012 -- Gardasil: Dr. Polansky Explains How Foreign DNA Fragments found in the Vaccine can Cause Disease
http://news.yahoo.com/dr-hanan-polansky-radio-explains-foreign-dna-fragments-081444139.html

Interesting read: Are you suffering from an infection with one of these viruses? (Product, Gene-Eden-VIR )
http://www.buy-gene-eden.com/

A doctor's comments, February 16, 2011 By Dr. Norman Cohen (Wisconsin)
http://www.buy-gene-eden.com/control-latent-viruses.php

Some of these scientific studies are listed on the Gene-Eden-VIR studies page.
http://www.buy-gene-eden.com/studies.php

Phage in Live Virus Vaccines: Are They Harmful to People?
http://www.sciencemag.org/content/187/4176/522.extract http://www.ncbi.nlm.nih.gov/pubmed/17769154

The Great HPV Vaccine Hoax Exposed
http://www.naturalnews.com/Report_HPV_Vaccine_0.html

Gardasil Vaccine Found to be Contaminated
http://sanevax.org/gardasil-vaccine-found-to-be-contaminated/

http://sanevax.org/

Gardasil Vaccine rDNA Introduced at Coroner’s Inquest
http://vactruth.com/2012/08/09/gardasil-rdna-coroners-inquest/

Bombshell Interview Reveals DNA Fragments Discovered 6 Months After Vaccination, (Gardasil) (and the girl, died)
http://vactruth.com/2012/08/16/rdna-fragments-after-vaccination/

HPV and HPV Vaccine - Facts and Truth
http://hpvfacts.co.uk/

Truth About Gardasil, (personal accounts of the harm done)
http://truthaboutgardasil.org/

HPV vaccine (Gardasil) – Seizures, Fainting, Paralyis, ….(Updated Chart)
(Endless more personal accounts of the HPV vaccine harm)
http://www.kkrasnowwaterman.com/blog/tabid/2962/bid/5747/HPV-vaccine-Gardasil-Seizures-Fainting-Paralyis-Updated-Chart.aspx

HPV Vaccines: Scientists Use Manufacturers’ Data to Prove Lack of Efficacy
http://gaia-health.com/gaia-blog/2012-10-28/hpv-vaccines-scientists-use-manufacturers-data-to-prove-lack-of-efficacy/

Is this vaccines actually doing more harm than good thing getting real to you yet? If not, go here to the next information. It gets worse.

BioWarfare: Mycoplasma - The Linking Pathogen in Neurosystemic Diseases
http://www.sott.net/article/155150-BioWarfare-Mycoplasma-The-Linking-Pathogen-in-Neurosystemic-Diseases

The Institute for Molecular Medicine, Garth Nicholson, PhD
http://www.immed.org/index.htm

Gulf War Illnesses Research
http://www.immed.org/illness/gulfwar_illness_research.html

WRITTEN TESTIMONY OF
Dr. Garth L. Nicolson
Special Oversight Board for Department of Defense Investigations of Gulf War Chemical and Biological Incidents
U. S. Senate Hart Office Building SH-216, November 19, 1998
http://gulfwarvets.com/testimony.htm

Vaccines Contaminated with Mycoplasma's - by Garth Nicolson

Garth Nicolson www.immed.org has written and published hundreds of peer reviewed medical journal articles. He discusses how vaccines are not tested for mycoplasma contamination's.

http://www.youtube.com/watch?v=Tk-RMI4qNvA

Chronic Diseases: Who's killing us, and how?
MICROBIOLOGIST GARTH NICOLSON
http://www.youtube.com/watch?v=lU12h6lWi9I

Garth Nicolson, Ph.D ILADS 2011 Presentation part 1 of 2

Dr. Nicolson, a renowned expert in mitochondrial research and lipid replacement therapy, spoke at the annual International Lyme and Associated Diseases Society Conference

http://www.youtube.com/watch?v=IKp4xCbNhag (Part 2) http://www.youtube.com/watch?v=BhdcR0VptWs

Now, lets ask another question as well. Do any of these vaccine contaminants, shed???? Meaning can they possibly be transferred through common human to human, transmission? And pro-vaccine states, oh no it is only the vaccinated that are at risk from the un-vaccinated? If they are at the CDC are that careless, inept, and in denial; that they would allow used a yearly-live nasal flu vaccine that is clearly known to shed; and even though the pharma clinical trials always downplay that percentage of chance; yet still plainly on the insert is the worded warning about shedding. Now, if that is not even an issue to the CDC, then what would be? And what happens every fall, when they start with the said flu mist? And they would claim it all of course to be a coincidence, and it to be only all part of the standard and known flu season, right? And it is all coincidental that the number of flu cases nearly immediately spiked. This is what they get away with.

And the CDC and the American Cancer Society, etc; all still make the same old claim, that there is no proof that SV 40 contamination in the previous polio vaccine ever caused any cancer. Even though in the 70's the number of cancer cases took to an increase that was obvious to everyone that eye sight and ears.

Lets take a look again at what actually happened here, below! Lets see how left out of the information loop the public has been left, and and as well mislead to be?

Scientific proof that the known cancer causing SV40 virus, a previous contaminant in the polio vaccine, is obviously either contagious; or the virus is still in the vaccine/s.
http://www.vacfacts.info/scientific-proof-that-the-known-cancer-causing-sv40-virus-a-previous-contaminant-in-the-polio-vaccine-is-obviously-either-contagious-or-the-virus-is-still-in-the-vaccines.html

60 Lab Studies Now Confirm Cancer Link to a Vaccine You Probably Had as a Child, SV40
http://www.thelibertybeacon.com/2013/02/24/60-lab-studies-now-confirm-cancer-link-to-a-vaccine-you-probably-had-as-a-child/

Merck Dr. ADMITS Cancer other Viruses Found In Vaccines, (SV-40)
http://www.youtube.com/watch?v=UXNluzIHq1k

Simian virus 40 in humans

To date, the prevalence of SV40 infections in humans is not known. Recent studies, based on PCR and serological techniques, indicate that SV40 infection occurs both in children and adults. (i) SV40 DNA sequences have been detected in normal and neoplastic tissues of people either too young (1 to 30 years) or too old (60 to 85 years) to have been vaccinated with SV40-contaminated anti-polio vaccines [19,33,76-81]. This finding may also explain the lack of difference in cancer incidence between individuals vaccinated with SV40-contaminated and SV40-free anti-polio vaccines [82]. (ii) SV40 sequences and Tag were detected in blood and sperm specimens from normal individuals and oncologic patients [80,81,83-88] and in lymphoblastoid cells [32]. These results suggest that (peripheral blood mononuclear cells) PBMCs, could be a reservoir and vehicle of SV40 spreading in the tissues of the host and among the individuals. (iii) SV40 sequences were found in urine and stoole samples, from children and adults [84,89,90], indicating that the haematic, sexual and orofecal routes of transmission are likely to be responsible for SV40 horizontal infection in humans.

Read more:
http://www.infectagentscancer.com/content/2/1/13

Failure Of The Continued Polio Vaccine Campaign
http://www.vacfacts.info/failure-of-the-continued-polio-vaccine-campaign.html

Post Vaccination - Vaccine Targeted Strain - Viral and Bacterial Pathogen - Shedding
http://www.vacfacts.info/post-vaccination-vaccine-targeted-strain---viral-and-bacterial---shedding.html

Chronic Viruses: The Common Cause of Most Cancers, (another, but not the only aspect in and as to the causation of cancer)
http://www.causeofcancer.org/

Biomedical Journals

The following peer-reviewed journals published reviews on the microcompetition with foreign DNA book:

http://www.cbcd.net/journals.htm

http://www.cbcd.net/book.htm

Latent infection and abnormal cell proliferation
By Hanan Polansky, November 7, 2002
http://www.cbcd.net/microcompetition.pdf

The Exploding Autoimmune Epidemic - Dr. Tent - It's Not Autoimmune Published on Dec 27, 2012
Well done Dr. Tent, now to get the world to come together and stop this madness.
http://www.youtube.com/watch?v=r8FCJ_VPyns

Failure Of The Continued Polio Vaccine Campaign

(With of course reference to obvious polio virus mutation occurring in the underdeveloped countries; using of course and of all things, the live oral polio vaccine. Increased at times virulence of the polio pathogen and with an intermix of the vaccine strain). Were those listed in this site page titled headlines, in your newspaper? Do you ask, why not?

http://www.vacfacts.info/failure-of-the-continued-polio-vaccine-campaign.html

Again. Pay close attention as well to this little expose. Actually read that said Gardasil VRBPAC 2006 preapproval document, recently of course non existent on the FDA’s website; for which a saved file copy was kept by Natural News. Quite obviously this vaccine should never have been approved, and the FDA clearly should have known that. And look at the outcome of that said FDA decision!

The Great HPV Vaccine Hoax Exposed
http://www.naturalnews.com/Report_HPV_Vaccine_0.html

Gardasil - The Real Truth
http://www.vacfacts.info/gardasil---the-real-truth.html

VACCINE CONTAMINATION: A THREAT TO HUMAN HEALTH
http://www.nvic.org/Downloads/Rotavirus-Campaign/VACCINE-CONTAMINATION--A-THREAT-TO-HUMAN-HEALTH.aspx
http://www.nvic.org/NVIC-Vaccine-News/May-2010/VACCINE-CONTAMINATION--A-THREAT-TO-HUMAN-HEALTH.aspx

---------------------------

Adventitious Agents and Vaccines Issue, Expose

Adventitious Agents and Vaccines
Philip R. Krause (go to full text pdf)
Food and Drug Administration, Bethesda, Maryland, USA
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2631857/

Full text:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2631857/pdf/11485673.pdf

Issues Associated With Residual Cell-Substrate DNA (I found Explorer worked to download this unbelievable read, and chrome did not)

(Page 20 and 47 mention the said WHO limit of 10ng of human DNA in a vaccine. But many of the current vaccines are produced with said human diploid tissue, and so what then? No mention of that issue appeared to have been made. As well see there reference made of ongogenic activity, and infective activity. Obviously they do not have any actual and nor sufficient animal and nor human studies on and in regard to this said issue. What they have is literally only presumed estimates. The FDA thus clearly knows of the cancer causing potential, infective potential, and of the unknown potential to create both known and unknown created adverse health situations with these vaccines; such as autoimmune disease as well Wow.)

www.fda.gov/ohrms/dockets/ac/05/slides/5-4188S1_4draft.ppt

New Study in Journal of Public Health and Epidemiology Correlates Autism Disorder Increase and Human Fetal DNA, Retroviral Agents in Vaccines

(My review of the information): So it should come as no surprise that the FDA has known for decades about the dangers of insertional mutagenesis by using the human fetal cell lines and yet, they chose to ignore it. Instead of conducting safety studies they regulated the amount of human DNA that could be present in a vaccine to no greater than 10ng. (See the FDA PDF reference link below titled, Issues Associated With Residual Cell-Substrate DNA)

Unfortunately, Dr. Deisher's team discovered that the fetal DNA levels in vaccines produced with aborted fetal cell tissue, ranged anywhere from 142ng - 2000ng per dose, way beyond the so-called "safe" level.

"There are a large number of publications about the presence of HERV (human endogenous retrovirus - the only re-activatable endogenous retrovirus) and its association with childhood lymphoma," noted Dr Deisher. "The MMR II and chickenpox vaccines and indeed all vaccines that were propagated or manufactured using the fetal cell line WI-38 are contaminated with this retrovirus. And both parents and physicians have a right to know this!"

Certainly these discoveries by SCPI should generate an immediate investigation by FDA officials, if not an outright ban on the use of aborted fetal cell lines as substrates for vaccine production. There are numerous other non-human FDA-approved cell lines that can and should be used.

New Study in Journal of Public Health and Epidemiology Correlates Autism Disorder Increase and Human Fetal DNA, Retroviral Agents in Vaccines
http://www.standardnewswire.com/news/965249574.html

Dr Deisher's study is available on the Academic Journals website at: www.ms.academicjournals.org/article/article1409245960_Deisher%20et%20al.pdf

Or on their website at www.soundchoice.org/scpiJournalPubHealthEpidem092014.pdf

CDC ADMITS THE PROBLEM

“- Many novel vaccines are produced in animal cell substrates, and emerging infectious diseases may theoretically be transmitted from animals to humans through these vaccines. The challenge of identifying potential adventitious agents in vaccines closely parallels the challenge of identifying the agents causing particular emerging infectious diseases.” http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2631857/pdf/11485673.pdf

Again, here go; two of the most important vaccine related articles you will ever find.

INDESCRIBABLY DISGUSTING VACCINE INGREDIENTS

SO WHAT ABOUT THE FLY IN OUR SOUP?

It may not do any harm at all, especially if it has been well heated in the soup!

However, all injected substances including insect fragments bypass the body’s intricate defense mechanism. The same substances which are harmless when ingested are shown to be extremely detrimental to health when injected. This is learned by medical students and others, but many doctors, health authorities and other vaccine promoters appear to ignore this basic fact.

Read more:
http://birthofanewearth.blogspot.com/2012/01/indescribably-disgusting-vaccine.html

If You Are In Support of Vaccinations, Read This If You Dare
http://www.thehealthyhomeeconomist.com/if-you-are-in-support-of-vaccinations/

Most of the below information is taken from the above two articles.

FDA: ONLY NONBINDING RECOMMENDATIONS FOR TESTING

There is no incentive for vaccine promoters to find substances which are detrimental to health. FDA only presents nonbinding recommendations:

“If an adventitious agent is known to be present in your cell substrate or viral seed, then you should demonstrate that your production process is sufficiently robust to eliminate or inactivate the agent with an appropriate margin of safety.” http://www.fda.gov/downloads/biologicsbloodvaccines/guidancecomplianceregulatoryinformation/guidances/vaccines/ucm202439.pdf

POSSIBLE CONSEQUENCES OF INJECTING FOREIGN DNA

“ – DNA is used from such organisms as animals, animal viruses, fungi, and bacteria. It has been documented that injecting foreign DNA in a human may cause it, or a portion of it, to be incorporated into the recipient’s DNA. The horrendous implications for the unborn defy the imagination.”http://healthwyze.org/index.php/vaccine-secrets.html

“- most vaccines are contaminated with a number of known and yet-to-be discovered viruses, bacteria, viral fragments, and DNA/RNA fragments. And, further, our science demonstrates that these contaminants could lead to a number of slowly-developing degenerative diseases, including degenerative diseases of the brain.” http://www.thehealthyhomeeconomist.com/if-you-are-in-support-of-vaccinations/

“- The risks of residual retinal DNA and stray viral contaminants from the animal tissues getting into flu shots are real. DNA snips are classified as either “infectious” or “oncogenic” (tumour causing) by researchers who worry that the stray DNA is being incorporated into the recipient’s DNA …”

Source:
http://www.newswithviews.com/Tenpenny/sherri123.htm

Interview with Dr. Suzanne Humphries. (Regarding contaminants from 33 minutes):
“- DNA particles from disease matter can get into our DNA and alter us and in my opinion these vaccines are turning us into genetically modified organisms.”

http://naturalnews.tv/v.asp?v=BAE7F6323813CFAFB8338173FB11D429

Here is another issue that they have. If Gardasil is EVER recalled, and AFTER all their LIES that is still found to be safe, they go directly under the GUN as to what they knew and when they knew it. Just like as to all vaccines, the CDC and FDA have all along known what was happening, and chose not to admit to it. A large spot light put on Gardasil, and as it will be if recalled, will then bring into the spotlight the contamination issues with all vaccines, and as well the safety.

Gardasil-The Flagship Example of the Failure of Vaccine Authorities to Regulate and Assure Vaccine Safety
“HPV Vaccine Has Done This to My Child”
http://www.vacfacts.info/gardasil-the-flagship-example-of-the-failure-of-vaccine-authorities-to-regulate-and-assure-vaccine-safety.html

SV40 VIRUS IS PASSED THROUGH GENERATIONS

“- many of the contaminant organisms can pass from generation to generation. For example, new studies have found that SV-40, a major contaminant of the polio vaccine until 1963, not only existed as a latent virus for the lifetime of those exposed to the vaccine but was being passed on to the next generation, primarily by way of sperm, something called vertical transmission. This means that every generation from now on will be infected with this known carcinogenic virus. There is also compelling evidence that some polio vaccines manufactured after 1963 may contain SV-40 virus. What makes the SV-40 contamination disaster of such concern is its association with so many cancers…”

http://www.thehealthyhomeeconomist.com/if-you-are-in-support-of-vaccinations/

“ – It is impossible to remove DNA contaminants from vaccines. Although weight limits for contaminating DNA were set by the FDA as far back as 1986, vaccine makers have never been able to reach that goal. The CDC decided to limit their weight recommendation to cancerous cell lines and then increase the other DNA contamination allowance one hundred-fold. However, these limits are only “recommendations” and, therefore, the FDA is unable to enforce them. Vaccine manufacturers continue to have the freedom to take scientific measures to reduce contaminants only if they wish.

http://www.opednews.com/populum/diarypage.php?did=14455

Simian virus 40 in humans

Fernanda Martini1, Alfredo Corallini2, Veronica Balatti1, Silvia Sabbioni2, Cecilia Pancaldi1 and Mauro Tognon1*

Corresponding author: Mauro Tognon

Author Affiliations

1 Department of Morphology and Embryology, Section of Cell Biology and Molecular Genetics, School of Medicine, and Center of Biotechnology, University of Ferrara, Via Fossato di Mortara, 64/B. 44100 Ferrara, Italy

2 Department of Experimental and Diagnostic Medicine, Section of Microbiology, University of Ferrara, Via Luigi Borsari, 46. 44100 Ferrara, Italy

To date, the prevalence of SV40 infections in humans is not known. Recent studies, based on PCR and serological techniques, indicate that SV40 infection occurs both in children and adults. (i) SV40 DNA sequences have been detected in normal and neoplastic tissues of people either too young (1 to 30 years) or too old (60 to 85 years) to have been vaccinated with SV40-contaminated anti-polio vaccines [19,33,76-81]. This finding may also explain the lack of difference in cancer incidence between individuals vaccinated with SV40-contaminated and SV40-free anti-polio vaccines [82]. (ii) SV40 sequences and Tag were detected in blood and sperm specimens from normal individuals and oncologic patients [80,81,83-88] and in lymphoblastoid cells [32]. These results suggest that (peripheral blood mononuclear cells) PBMCs, could be a reservoir and vehicle of SV40 spreading in the tissues of the host and among the individuals. (iii) SV40 sequences were found in urine and stoole samples, from children and adults [84,89,90], indicating that the haematic, sexual and orofecal routes of transmission are likely to be responsible for SV40 horizontal infection in humans.

Read more:
http://www.infectagentscancer.com/content/2/1/13

Advances in Virus Research, Volume 50

Pages 83 and 84, read. (Also see the study titled, Simian virus 40 in humans, below on this page)

Excerpted:

Moreover, blood and sperm fluid may represent important means for spreading of SV40 in humans.

Indeed in these investigations, (Martini etal;, 1995,1996) 61% of the neoplastic patients positive for SV 40 sequences were of an age excluding exposure to SV 40-contaminated polio vaccines, suggesting contagious transmission of SV 40 by horizontal infection.

http://books.google.com/books?id=PfO7D8ZoSMkC&pg=PA84&lpg=PA84&dq=sv40+is+contagious&source=bl&ots=AlaWsAkp95&sig=RnycQFX2ucD-3zybHQ07FAIeJYk&hl=en&sa=X&ei=kZLfT5_mA4qc2QXKz6jtCA&ved=0CFoQ6AEwBg#v=onepage&q=sv40%20is%20contagious&f=false

SV-40 Deadly Cure
http://www.viewzone.com/sv40x.html

Types of SV40 Associated Cancers:
http://www.sv40foundation.org/Types.html