The American Centers for Disease Control CDC has admitted that between 1955–1963 over 98 million Americans received one or more doses of a polio shot which was contaminated with a cancer-causing virus called Simian vacuolating virus 40 (SV40).
The CDC quickly took down the page, along with Google, but the site was luckily cached and saved to symbolize this grand admission.
According to an official statement of the CDC, they estimated that somewhere between 10 and 30 million Americans might have received the SV40-contaminated vaccine during that period.
SV40 is an abbreviation for Simian vacuolating virus 40 or Simian virus 40, a polyomavirus that is found in both monkeys and humans. Like other polyomaviruses, SV40 is a DNA virus that has been found to cause tumors and cancer.
SV40 is believed to suppress the transcriptional properties of the tumor-suppressing genes in humans through the SV40 Large T-antigen and SV40 Small T-antigen. Mutated genes may contribute to uncontrolled cellular proliferation leading to cancer.
To go further and confirm this unbelievable admission, Assistant Professor of Pathology at Loyola University in Chicago Dr. Michele Carbone has been able to independently verify the presence of the SV40 virus in tissue and bone samples from patients who died during that era.
He found that 33% of the samples with osteosarcoma bone cancers, 40% of other bone cancers, and 60% of the mesothelioma’s lung cancers all contained this obscure virus.
This leaves the postulation that upwards of 10–30 million actually contracted and were adversely affected by this virus, to be deadly accurate.
The CDC has quickly removed a page from their website, which was cached here admitting that more than 98 million Americans received one or more doses of polio vaccine within an 8-year span from 1955-1963 when a proportion of the vaccine was contaminated with cancer-causing polyomavirus called SV40.
Michele Carbone, Assistant Professor of Pathology at Loyola University in Chicago, has recently isolated fragments of the SV-40 virus in human bone cancers and in a lethal form of lung cancer called mesothelioma.
He found SV-40 in 33% of the osteosarcoma bone cancers studied, in 40% of other bone cancers, and in 60% of the mesotheliomas lung cancers, writes Geraldo Fuentes.
Dr. Michele Carbone openly acknowledged HIV/AIDS was spread by the hepatitis B vaccine produced by Merck & Co. during the early 1970s.
It was the first time since the initial transmissions took place in 1972-74, that a leading expert in the field of vaccine manufacturing and testing has openly admitted the Merck & Co. liability for AIDS.
The matter-of-fact disclosure came during discussions of polio vaccines contaminated with an SV40 virus which caused cancer in nearly every species infected by injection.
Many authorities now admit much, possibly most, of the world’s cancers came from the Salk and Sabin polio vaccines, and hepatitis B vaccines, produced in monkeys and chimps.
It is said mesothelioma is a result of asbestos exposure, but research reveals that 50% of the current mesotheliomas being treated no longer occurs due to asbestos but rather the SV-40 virus contained in the polio vaccination.
In addition, according to researchers from the Institute of Histology and General Embryology of the University of Ferrara, SV-40 has turned up in a variety of other tumors.
By the end of 1996, dozens of scientists reported finding SV40 in a variety of bone cancers and a wide range of brain cancers, which had risen 30 percent over the previous 20 years.
A Greater Perspective on Aerial Spraying and SV40
The Defense Sciences Office of the Pathogen Countermeasures Program, on September 23, 1998, funded the University of Michigan’s principal investigator, Dr. James Baker Jr., Director of Michigan Nanotechnology Institute for Medicine and Biological Sciences under several DARPA grants.
Dr. Baker developed and focused on preventing pathogens from entering the human body, which is a major goal in the development of countermeasures to Biological Warfare.
This research project seeks to develop a composite material that will serve as a pathogen avoidance barrier and post-exposure therapeutic agent to be applied in a topical manner to the skin and mucous membranes.
The composite is modeled after the immune system in that it involves redundant, non-specific, and specific forms of pathogen defense and inactivation.
This composite material is now utilized in many nasal vaccines and vector control through the use of hydro-gel, nano silicon gels, and actuator materials in vaccines.
Through Dr. Baker’s research at the University of Michigan; he developed dendritic polymers and their application to medical and biological science. He co-developed a new vector system for gene transfer using synthetic polymers.
These studies have produced striking results and have the potential to change the basis of gene transfer therapy.
Dendrimers are nanometer-sized water-soluble polymers that can conjugate to peptides or carbohydrates to act as decoy molecules to inhibit the binding of toxins and viruses to cells.
They can act also as complex and stabilize genetic material for prolonged periods of time, as in a “time-released or delayed gene transfer”.
Through Dr. Baker’s groundbreaking research many pharmaceutical and biological pesticide manufacturers can use these principles in DNA vaccines specific applications that incorporate the Simian Monkey Virus SV40.
West Nile Virus Spraying
In 2006, Michael Greenwood wrote an article for the Yale School of Public Health entitled, “Aerial Spraying Effectively Reduces Incidence of West Nile Virus (WNV) in Humans.
The article stated that the incidence of human West Nile virus cases can be significantly reduced through large-scale aerial spraying that targets adult mosquitoes, according to research by the Yale School of Public Health and the California Department of Public Health.
Under the mandate for aerial spraying for specific vectors that pose a threat to human health, aerial vaccines known as DNA Vaccine Enhancements and Recombinant Vaccine against WNV may be tested or used to “protect” the people from vector infection exposures.
DNA vaccine enhancements specifically use Epstein-Barr viral capsid with multi-human complement class II activators to neutralize antibodies.
The recombinant vaccines against WNV use Rabbit Beta-globulin or the poly (A) signal of the SV40 virus. In early studies of DNA vaccines, it was found that the negative result studies would go into the category of future developmental research projects in gene therapy.
During the studies of poly (A) signaling of the SV40 for WNV vaccines, it was observed that WNV will lie dormant in individuals who were exposed to chickenpox, thus upon exposure to WNV aerial vaccines, the potential for the release of chickenpox virus would cause a greater risk to having adult-onset Shingles.
California Aerial Spraying for WNV and SV40
From February 2009 to the present date, aerial spraying for the WNV occurred in major cities within the State of California. During spraying of Anaheim, CA, a Caucasian female (age 50) was exposed to heavy spraying while doing her daily exercise of walking several miles.
Heavy helicopter activity occurred for several days in this area. After spraying, she experienced lightheadedness, nausea, muscle aches, and increased low back pain.
She was evaluated for toxicological mechanisms that were associated with pesticide exposure due to aerial spraying utilizing advanced biological monitoring testing.
The test results which included protein band testing utilizing Protein Coupled Response (PCR) methods were positive for KD-45. KD-45 is the protein band of the SV-40 Simian Green Monkey virus.
Additional tests were performed for Epstein-Barr virus capsid and Cytomeglia virus which is used in bioengineering for gene delivery systems through viral protein envelope and adenoviral protein envelope technology.
The individual was positive for both; indicating a highly probable exposure to a DNA vaccination delivery system through nasal inhalation. The question of the century is how many other viruses and toxins are within current day vaccines that we’ll only find out about in a few decades?
Aluminum gels or aluminum salts are vaccine ingredients that have been used in vaccines since the 1930s. Small amounts of aluminum are added to help the body build stronger immunity against the germ in the vaccine.
Aluminum is one of the most common metals found in nature and is present in air, food, and water. The amount of aluminum present in vaccines is low and is regulated by the U.S. Food and Drug Administration (FDA).
http://www.cdc.gov/vaccinesafety/Concerns/adjuvants.html
Abstract
Aluminum is an experimentally demonstrated neurotoxin and the most commonly used vaccine adjuvant. Despite almost 90 years of widespread use of aluminum adjuvants, medical science’s understanding of their mechanisms of action is still remarkably poor.
There is also a concerning scarcity of data on the toxicology and pharmacokinetics of these compounds. In spite of this, the notion that aluminum in vaccines is safe appears to be widely accepted.
Experimental research, however, clearly shows that aluminum adjuvants have the potential to induce serious immunological disorders in humans.
In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation, and associated neurological complications and may thus have profound and widespread adverse health consequences.
In our opinion, the possibility that vaccine benefits may have been overrated and the risk of potential adverse effects underestimated has not been rigorously evaluated in the medical and scientific community.
We hope that the present paper will provide a framework for a much-needed and long-overdue assessment of this highly contentious medical issue.
http://www.ncbi.nlm.nih.gov/pubmed/21568886
Editorial
When I started my carrier in the medical field in 1969, I noticed within three years criminal activities carried out by military, pharmaceutical, medical and political establishments.
I had mentioned to my educators about the vaccination and vaccine safety problems such as was given to patients and in the military to fight respiratory and many other infections. For instance, our patients didn’t die of graft rejection but of Aids because of used medications.
Within the military, through the Vietnam era, was the only organization allowed to use the adenovirus vaccinations, as a matter of “national security,” since the adenovirus infections, although relatively mild for most infected, was so contagious, that it could temporarily disable a large number of military members.
As a consequence that particular vaccine only was outlawed for use on civilians since it was known to cause leukemia.
In my opinion, the fact that so many Vietnam era vets were coming down with leukemia had far more to do with the vaccinations for adenovirus prevention than Agent Orange or any other factor involved with service in the military during Vietnam.
It has since been discontinued by the military.
Secrets of HIV-Aids Journal 