by Leslie Carol Botha
from HolyHormones Website
Foreign DNA is a term most medical consumers are not aware of.
However, common sense alone raises questions about the dangers of foreign DNA - otherwise known as recombinant DNA. The American Biologic Safety Association (ABSA) has classified recombinant DNA a biohazard and has outlined specific directives over the handling of such contaminants.1
According to a supporting document, written by the Coalition of Vaccine Safety,
The Center for the Biology of Chronic Disease (CBCD),* publisher of Dr. Hanan Polansky’s the Purple book Microcompetition with Foreign DNA and the Origin of Chronic Disease explains how foreign DNA fragments can cause many major diseases without damaging (mutating) the human DNA.
The book has been read by more than 5,000 scientists around the world, and has been reviewed in more than 20 leading scientific journals. The theory explains the underlying cause of many major diseases and shows how dormant viruses actually can cause disease while still latent.
Dr. Polansky discovered that foreign DNA fragments called N-boxes can cause disease. When these foreign DNA fragments enter the body (naturally, or artificially, like through an injection of a vaccine or other treatments), they end up in the cell’s nucleus, where they attract scarce genetic resources.
The “microcompetition” between the foreign N-boxes and the human N-boxes cause the human genes to malfunction, which, in turn, can lead to disease.
In fact, when approached about the HPV rDNA contamination found in Gardasil® - Dr. Polansky agreed that the contaminant should not be there.
According to Polansky - the potentially harmful contaminant is part of the faulty biologic medicine manufacturing process that is unable to filter out all foreign DNA plasmids and therefore the particles were suspected to be present in all biologic medicines on the market.
In April of this year, the CBCD published a press release4 encouraging the CDC to study Polansky’s Microcompetition Theory since foreign DNA has also been found in Merck & Co.’s MMR II vaccine.5
The vaccine package insert (available for download at the FDA’s web site) shows that fetal cell line Wistar RA 27/3, fetal cell line WI-38, and genetically engineered human albumin are all used in the vaccine.
The CBCD believes that a better understanding of the theory - lauded by many scientists and researchers at NIH, and other esteemed universities and organizations may lead to better policies to curb the Autism epidemic. In a recent CDC report that epidemic has increased by 78% since 2007.
Infants 12 months of age or older, are inoculated with the MMR II vaccine with a second dose usually given around age four or five right before entry to school. According to the CBCD, this is also usually the time that the majority of Autism diagnoses are made.
The release goes on to state:
However, it appears that the CDC and FDA are aware of the problem with vaccines.
In June of 2001, a paper was published in Emerging Infectious Diseases entitled: “Adventitious Agents and Vaccines” stating that:
Dormant HPV Infections the Silent Culprit
Although the FDA asserts that the foreign DNA fragments found in Gardasil® poses no risk, the CBCD disagrees.
Their research has led them to believe that HPV has the ability to establish a chronic, dormant (latent) infection and it those chronic infections that can potentially lead to cancer.
A recent study entitled “Prevalence of Oral HPV Infection in the United States, 2009 - 2010” that was published in the Journal of the American Medical Association (JAMA) reported that the HPV virus was found in the mouths of 7% of study participants. 5,600 people participated in the study.
Oral HPV was found in men more than in women.
The authors of the study wrote,
In essence, according to the study, 2.13 million people who don’t have symptoms now, and don’t even know they are infected, could develop cancer due to their HPV infection. 7
Now add in the rDNA factor and one has to wonder at the mechanisms of action that are actually going on in the body.
Dormant DNA - potentially becoming stimulated by the vaccine designed to prevent the chronic infection leading to cervical and other HPV-related cancers - with a mix of rDNA bound to aluminum now circulating in the blood and targeting the weakened areas of the body.
HPV rDNA Particles found in Postmortem Inquest of New Zealand Girl
In August, Dr Sin Hang Lee, a pathologist on the medical staff at Connecticut’s Milford Hospital testified about the discovery of HPV DNA fragments in post-mortem samples of her blood and spleen 6 months after Gardasil®® vaccination at the postmortem inquest of Jasmine Renata, a New Zealand teenager who died in her sleep.8
Dr. Lee’s testimony stated:
Although Dr. Lee’s discovery cannot directly tie the rDNA to the girl’s death, the probable mechanism of action does exist since all other ‘cause of death’ scenarios have been ruled out.
According to Dr. Lee, Gardasil® contains a genetically engineered recombinant HPV DNA inserted into yeast cells. rDNA behaves differently than natural HPV DNA which does not stay in the blood stream for a long period of time.
Once a segment of recombinant DNA is inserted into a human cell, the consequences are hard to predict.
It may be in the cell temporarily or stay there forever, with or without causing a mutation. Now the host cell contains human DNA as well as genetically engineered viral DNA. 9
War of the DNA
The most frightening aspect of all is that government health agencies do not have the testing nor do they have understanding as to what happens when a recombinant DNA particle infects a cell with ‘normal’ DNA.
What are the mechanisms of action that determine who wins the DNA wars? What if the normal ‘DNA’ loses? Are the skyrocketing rates of autism and the increasing Post-Gardasil and Post-Cervarix Syndromes examples of DNA gone bad?
Even more frightening is that scientists do not know how to isolate or even remove the foreign DNA particles from the body.
What lies ahead is a crap shoot for medical consumers who are left with a,
* Note: The Center for the Biology for Chronic Disease web site is currently offline. I spoke with them last week and was made aware of the press release they published last April - Autism Epidemic, Is Foreign DNA in MMR II Vaccine Responsible? CBCD Suggests CDC Study Microcompetition Theory. It is reprinted here in full in case the online version becomes unavailable.
** Note: As of mid-August the CBCD have stopped answering their phones. In fact, upon calling - one gets a recorded message saying ‘this phone call may be recorded’ even before hearing the dial tone. I was told that Dr. Polansky was going to approve my article. However, all email communications have now ceased.
Radio interview with Dr. Polansky on February 4, 2012 - Gardasil: Dr. Polansky Explains How Foreign DNA Fragments found in the Vaccine can Cause Disease
Rochester, NY (PRWEB)
April 04, 2012
The CDC’s latest report on Autism says,
Autism rates have gone up by 25% in just two years. In fact, the latest CDC report marks a 78% increase since its first report on Autism in 2007. Experts call it an epidemic. 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.
The CDC must be aware of the existence of foreign DNA in the MMR II vaccine. However, the CDC may be unaware of the relationship between foreign DNA and Autism as explained by the Microcompetition theory.
The CDC is aware of the public demand to find the cause of the epidemic.
According to the CDC,
The CBCD urges CDC officials to become familiar with the Microcompetition theory as described in Dr. Hanan Polansky’s “Purple Book,” which has been available as a free public access download from the CBCD website since 2003.
A better understanding of the theory may lead to better policies to curb the Autism epidemic.
As mentioned above, the MMR II vaccine contains foreign DNA fragments. The MMR II vaccine is given to infants 12 months of age or older, with a second dose usually given around age four or five right before starting school. Perhaps not so coincidentally, this is also usually the time that the majority of Autism diagnoses are made.
Surely, the CDC knows that information regarding DNA fragments contaminating the MMR II is available to the public as a download from the FDA’s website. 
One can download the vaccine package insert for the MMR II vaccine written by Merck & Co., Inc. which shows that Fetal cell line Wistar RA 27/3, Fetal cell line WI-38, and genetically engineered human albumin are all used in the vaccine.
The CBCD believes that the current purification processes cannot completely filter all foreign DNA plasmids used in the process of manufacturing the MMR II vaccine.
Therefore, some foreign DNA fragments end up being injected into infants.
Microcompetition between the foreign DNA fragments injected into infants through the MMR II vaccine and the child’s own DNA could be the biological mechanism linking the MMR II vaccine to Autism.
With the above information in mind, the CBCD especially encourages the CDC and NHS to conduct research into this area and fund studies to either confirm or deny the CBCD’s suspicions.
The CBCD also encourages CDC, NHS, and FDA officials, as well as virologists, biologists, geneticists, scientists, physicians and the public to obtain a copy of Dr. Hanan Polansky’s book and read it.
The CBCD endorses Dr. Polansky’s theory and invites family doctors, pediatricians, scientists, the media, and the public to contact us on this issue.
For more information on the Center for the Biology of Chronic Disease, or to schedule an interview with Dr. Polansky, please visit http://www.cbcd.net or call 585-250-9999.