Untested Toxicity Found in Gardasil Vaccine

HPV DNA bound to insoluble aluminum adjuvant.

By NORMA ERICKSON | SANEVAX | OCTOBER 19, 2012

Genetic modification of food has come under severe criticism from the scientific community as new health risks are being discovered. Do genetically modified vaccines carry any less risk? The study below outlines just a few of the unanswered questions about one of the genetically engineered vaccines currently in use, namely Gardasil®.

Dr. Sin Hang Lee of Milford Hospital recently published an article in The Journal of Inorganic Biochemistry entitled, Detection of human papillomavirus (HPV) L1 gene DNA possibly bound to particulate aluminum adjuvant in the HPV vaccine Gardasil®.

According to Dr. Lee’s research (sponsored by SaneVax Inc.), during the manufacture of Gardasil, Merck may have inadvertently created a new chemical compound composed of HPV L1 gene fragments chemically bound to the aluminum nanoparticles of the AAHS adjuvant used in the vaccine.

If this is true, the toxicity of this chemical has not been tested. No one knows what the potential health consequences the injection of this ‘ingredient’ may be.

Consider some key points extracted from the article by Dr. Lee:

A total of 16 samples of Gardasil® received from Australia, Bulgaria, France, India, New Zealand, Poland, Russia, Spain and the United States were found to contain fragments of HPV-18-L1 gene DNA which was readily detected in 15 of 16 samples tested, or HPV-11-L1 gene DNA, or a mixture of both. After submission of the manuscript, HPV-16-L1 gene fragments were also detected among these samples by a special protocol, Dr. Lee noted in his report.

Dr. Lee stated:

“Although the U.S. Food and Drug Administration recently announced that Gardasil® indeed does contain recombinant HPV L1-specific DNA fragments, the physical condition(s) of these HPV DNA fragments in the final vaccine product has not been characterized.”

Dr. Lee presented experimental evidence to assert that the binding mechanism between the HPV L1 gene DNA and the amorphous aluminum hydroxyphosphate sulfate (AAHS) nanoparticles in Gardasil® is of a chemical nature through ligand exchange of phosphate for hydroxyl, independent of the electrostatic forces. When aluminum (Al3+) and DNA interact, the binding site for Al3+ on the DNA chains is the phosphate groups on the DNA backbones.

For the average medical consumer, if the bond between the DNA and aluminum were electrostatic, it would be much like when you rub a balloon against your head until the static electricity builds up to the point where you can stick the balloon to a wall. As you may have noticed, given a short period of time, the balloon loses the static electric charge and falls off the wall. This is much the same as a vaccine in which the bond between the antigen and adjuvant is electrostatic. Once the vaccine is injected, the recipient’s normal pH level reduces the electrostatic attraction making the antigen and adjuvant separate from each other.

On the other hand, if the bond between the DNA and aluminum is chemical, it is more like taking a blob of super-glue and sticking the balloon to the wall. In this instance, no one knows how long the bond will remain intact.

In light of this substantial difference, Dr. Lee concluded:

“The short-term and long-term impact of the residual fragments of HPV L1 gene DNA, or plasmid DNA, if chemically bound to the mineral aluminum of AAHS nanoparticles is largely unknown and warrants further investigation.”

In Sept 2011, the SaneVax Team informed the FDA that HPV DNA fragments had been found firmly attached to the aluminum adjuvant in 100% of Gardasil samples tested by Dr. Sin Hang Lee of Milford Hospital.

The FDA response included the following statement with no references to back it up:

“Recombinant technology has been used for many years to manufacture medicinal products. Gardasil does contain HPV L1-specific DNA fragments. This is expected, since DNA encoding the HPV L1 gene is used in the vaccine manufacturing process to produce the virus-like particles. The presence of these expected DNA fragments, which are inevitable in vaccine production, is not a risk to vaccine recipients, is not harmful, and this DNA is not a contaminant.”

As you can clearly see, there is no mention whatsoever is made about these fragments possibly being firmly attached to the aluminum adjuvant. The SaneVax Team as well as many eminent scientists and medical professionals around the world believe this ‘tiny’ detail should not be ignored.

If this ‘ingredient’ is indeed an ‘inevitable’ component of recombinant technology, medical consumers have a right to know when, for how long and under what circumstances it was tested for safety.

After an entire year of multiple communication attempts receiving no scientific documentation from the FDA that this ‘ingredient’ did not pose a health threat, the SaneVax Team sent another letter to the FDA Commissioner with one simple request.

This letter asked for copies of documents from the FDA showing:

1)    The date when the FDA and the manufacturer first knew small quantities of residual recombinant HPV L1-specific DNA fragments remain in the vaccine.

2)    The physical condition of the HPV- L1-specific DNA fragments in the Gardasil® vaccine.

To date, the FDA has made no effort to respond to this request. Do they have any documentation? If so, why do they not provide this critical information to medical consumers?

Surely, considering the fact that these fragments are an ‘inevitable’ component of recombinant technology, they have requested safety studies to determine any potential health impact. After all, they are responsible for the health and safety of medical consumers – aren’t they?

One more critical point:

Why did Merck not detect the residues of HPV-18-L1 gene DNA during the production of Gardasil®?

Dr. Lee offered the following explanation:

“…all HPV-18 isolates can be classified into 3 subtypes based on alignments of the DNA sequences of the variants, (i.e. the European, the Asian-American and the African subtypes). In Europe, it has been reported that all of the HPV-18 isolates from patients are found to be of the European or Asian-American variants. In the U.S., 91% of the HPV-18 isolates from white women are reported to be of the European and Asian-American variants, and 64% of the HPV isolates from African American women belong to the African variant.

Since the prevalence of the African variants of HPV-18 among European patients is negligible, the Dutch researchers who originally developed the HPV INNO-LIPA kit naturally selected an HPV-18 probe targeting a homologous sequence shared by all European and Asian-American HPV-18 variants for the testing.

However, the HPV-18 L1 protein-coding gene chosen by the manufacturer for Gardasil® closely related to an African subtype. Failure to detect a target sequence of an African variant HPV-18 DNA in the vaccine Gardasil® with a hybridization probe specifically designed for the European and Asian-American DNA variants may simply reflect the diversity of the L1 protein amino acid sequences within the genotype of HPV-18.”

For medical consumers, this brings additional questions. Has Gardasil® been tested for efficacy against all three HPV-18 variants?

Are families in the United States and Europe putting their children at risk of unknown health consequences resulting from the injection of a new chemical with untested toxicity in order to obtain ‘protection’ against only one type of oncogenic HPV?

The time has come for medical consumers to hold their national health ‘authorities’ accountable. These questions must be answered before any more children become ‘one less.’

(Note: Dr. Lee’s study was commissioned and sponsored by SaneVax Inc. for a future payment not to exceed one U.S. dollar.)

Ganancias de Merck Aumentan Vertiginosamente de la mano de Gardasil

La corporación farmacéutica es respaldada por el aumento sin precedentes en el uso de la peligrosa vacuna Gardasil.

Anthony Gucciardi
NaturalSociety
03 de noviembre 2011

El mega fabricante de medicamentos Merck & Co. reporta un aumento importante de ganancias del tercer trimestre, debido en parte a las ventas de su producto símbolo, la vacuna Gardasil, que ha sido vinculada a enfermedades y reacciones negativas en pacientes – un aumento de 41 por ciento a $ 445 millones – gracias al apoyo del gobierno y las campañas publicitarias engañosas de gran éxito dirigidas a los padres y los niños inocentes. El valor total de las acciones de Merck subieron 80 centavos, o 2,3 por ciento, a 35,11 dólares. Los números son mayores que hace un año, cuando la compañía se vio afectada con adquisiciones y los gastos legales. Por supuesto que detrás del aumento en las ventas de Gardasil están las corruptas políticas y técnicas de comercialización utilizadas para impulsar la política de Merck.

Cuando se trata de Gardasil, Merck está más preocupada por inyectar a los niños y generar un beneficio que de examinar los verdaderos efectos de la inyección. Merck empuja Gardasil a los niños a través de la omisión de hechos, el soborno político y las mentiras descaradas.

¿Cómo podría Merck vender Gardasil en cantidades tan altas a pesar de la documentación que la vincula a 3.589 reacciones dañinas y 16 muertes entre mayo de 2009 y septiembre de 2010? Bueno, Merck le gusta pretender que la relación entre su producto y la muerte de pacientes no existe. Además, Merck utiliza incentivos monetarios, también considerados como soborno, para asegurar que la legislación pro Gardasil es rápidamente aprobada por los legisladores. Porque cuando se trata de generar beneficios, Merck no tiene ninguna preocupación por la salud de un individuo – especialmente la población objetivo de niños y niñas entre las edades de 11 y 12.

Con el fin de impulsar Gardasil como una vacuna “segura”, Merck va tan lejos como mentir descaradamente sobre los efectos secundarios de la vacuna contra el VPH en anuncios de revistas, anuncios en internet, e incluso en el sitio web oficial de Gardasil. En mi informe especial sobre los anuncios de Gardasil, documenté cómo Merck esconde los efectos secundários de la vacuna, como la muerte y el síndrome de Guillain-Barré con otros menos amenazantes tales como dolor de cabeza y náuseas.

En cuanto a la corrupción política, Merck ha sido expuesta por Cal Watchdog sobornando legisladores clave en California con miles de dólares. Por supuesto, estos legisladores clave jugaron un papel decisivo en la aprobación de la ley que ahora permite que niños de 12 años puedan decidir por sí solos aceptar o no la vacuna Gardasil sin el consentimiento de los padres. Teniendo en cuenta la información engañosa acerca de la vacuna VPH Gardasil, es razonable creer que estos niños se consideran que la vacuna es relativamente inofensiva. Desafortunadamente, aquellos que no siguen las noticias sobre la salud son a menudo en la oscuridad sobre los peligros Gardasil.

Los peligros de Gardasil son tan extensos que se ha hecho una línea de tiempo para documentar los efectos secundários en los últimos meses. A medida que más información sigue saliendo, Merck pronto podría ver una disminución significativa en las ventas de Gardasil.

 

Merck’s Profits Explode as Government-Backed HPV Shot Gardasil Sales Skyrocket

Anthony Gucciardi
NaturalSociety
November 1, 2011

Mega drug manufacturer Merck & Co. is reporting a major increase in third-quarter profits due in part to the skyrocketing sales of death-linked HPV shot Gardasil – up 41 percent to $445 million thanks to government backing and a hugely successful yet deceptive ad campaigns targeted at unsuspecting parents and children. The overall value of Merck shares rose 80 cents, or 2.3 percent, to $35.11. The numbers are up from a year ago, when the company was hit with huge acquisition and legal charges. Of course behind  the monetary surge in Gardasil sales is the horribly corrupt marketing and political techniques used to boost Merck out of economic downfall.

When it comes to Gardasil, Merck is more concerned about pushing the shot on children and generating a profit than examining the true effects of the shot.

 Merck pushes Gardasil on children through omission of facts, political bribery, and blatant lies

How could Merck sell Gardasil in such high quantities despite documentation linking it to  3,589 harmful reactions and 16 deaths between May 2009 and September 2010 alone? Well, Merck likes to pretend that the death link does not exist. Furthermore, Merck uses monetary incentive, also considered bribery, to ensure that Gardasil legislation is swiftly passed by key legislators. Because when it comes to generating profit, Merck has no concern for the health of the individual — especially the target demographic of boys and girls between the ages of 11 and 12.

In order to push Gardasil as a “safe” vaccine, Merck will go as far as to blatantly lie about the side effects of the HPV shot in magazine ads, website banner ads, and even on the official Gardasil website. In my special report on Gardasil ads, I documented how Merck supplements the real known side effects of Gardasil such as death and Guillain-Barre Syndrome for less threatening ones such as headache and nausea.

As for political bribery, Merck has been caught by Cal Watchdog supplying key California legislators with thousands of dollars. Of course these key legislators were instrumental in the passing of the Gardasil bill that now allows for 12 year old children to decide whether or not they would like to be injected with the Gardasil vaccine without any parental consent. Given deceptive information about the HPV shot Gardasil, it is reasonable to believe that these young children would consider the shot to be relatively harmless. Unfortunately, those who do not follow health news are oftentimes in the dark over Gardasil dangers.

The dangers of Gardasil are so extensive that a timeline has been made documenting just the past several months in developments. As more information continues to come out, Merck may soon see a significant decrease in Gardasil profits.

AIDS: The Greatest Mass Synthetic Weapon

Funded by Congress in 1969 Through House Bill 15090, the AIDS Virus was Created After 1974

By Luis R. Miranda
The Real Agenda
November 5, 2007

Proof that the AIDS virus is man-made and not naturally born, pile on as more information turns public and access to more and moreAIDS documents that reach more and more people become available. The account that the AIDS virus was originally found in a monkey, and that from it, the virus somehow jumped to humans has been debunked; to use a popular term.

The most eye-opening piece of evidence is government documents; more specifically the House of Representatives H.R 15090 from 1969 which details how and when the second branch of government held hearings and funded a project in which the Department of Defense would utilize $10 million to research and create a synthetic virus that would then be tested in humans in the form of an injection.

After ten years of investigation, the virus was created sometime after 1974 and was experimented with by injecting humans as early as 1977. Although in the US the Department of Defense requested the financing and promoted the creation of the virus, entities like the World Health Organization and the United Nations had previously called for a bio weapon of the sort. The World Health Organization (WHO), started to inject AIDS -laced smallpox vaccine into Africans in 1977, while the Center for Disease Control (CDC) injected some 2000 white males with laced Hepatitis B vaccine in 1978.

According to the Strecker Memorandum of 1983, AIDS is a man-made disease, which is not specific of homosexuals, not venereal and which can be carried by mosquitoes. In addition, it is clear that although condoms would help reduce the chances of infection, they would not prevent the at least six types of AIDS viruses available. Dr. Theodore Strecker writes: “The US National Cancer Institute in collaboration with the World Health Organization manufactured AIDS in a laboratory at Fort Detrich, Maryland.” The AIDS virus is a combination of two retroviruses. One is the Bovine Leukemia Virus, and the second the Visna Virus which were injected into human tissue in its early stages in order to see the results.

Dr. Strecker states that the AIDS virus could not be naturally born and that were virologists who worked in the creation of an organism that could exert selective influence in the way the human body fights infection. The possibility was looked into that the virus impaired the immune system so that it could not respond once it made its way into the human body. According to the Strecker memo, the AIDS epidemic was triggered by the mass vaccination campaign that intended to end Smallpox.

The following is an exact transcription of the narrative in the Subcommittee of Appropriations held in July 1, 1969, which involved discussions about Synthetic Biological Agents.

There are two things about the biological agent field I would like to mention. One is the possibility of technological surprise. Molecular biology is a field that is advancing very rapidly and many eminent biologists believe that within a period of 5 – 10 years it would be possible to produce a synthetic biological agent, an agent that does not naturally exist and for which no natural immunity could have been acquired.”

Mr. Sikes: Are we doing any work in that field?

Dr. MacArthur: We are not.

Mr. Sikes: Why not? Lack of money or lack of interest?

Dr. MacArthur: Certainly not lack of interest.

Mr. Sikes: Would you provide for our record information on what would be required, what the advantages of such a program would be, the time and the cost involved?

Dr. MacArthur: We will be very happy to. The dramatic progress being made in the field of molecular biology led us to investigate the relevance of this field of science to biological warfare. A small group of experts considered this matter and provided the following observations:

1. All biological agents up to the present time are representatives of naturally occurring disease, and are thus known by scientists throughout the world. They are easily available to qualified scientists for research, either for offensive or defensive purposes.

2. Within the next 5 – 10 years, it would probably be possible to make a new infective microorganism which could differ in certain important aspects from any known disease-causing organisms. Most important of these is that it might be refractory to the immunological and therapeutic processes upon which we depend to maintain our relative freedom from infectious disease.

3. A research program to explore the feasibility to this could be completed in approximately 5 years at a cost of $10 million.

As it has been documented, the World Health Organization used the Smallpox vaccine to spread the virus in Africa, Haiti, Brazil and Japan. After looking for documents to support the statement, it is clear that the spread of the virus coincides with how this plan was originally laid out. As an addendum, a confidential source in the WHO has revealed that there is “a strong correlation between the proportion of people in different central African countries who consented to the smallpox vaccine program and the proportion of those now infected with AIDS.

In the last fifteen years, the AIDS virus has killed 11 million Africans, which accounts for a total of 80 percent of the total world deaths due to the virus. According to numbers provided by the United Nations, at least 5000 funerals are held daily in Africa for people who die as a consequence of contracting the AIDS virus. Outdated numbers from 2001 show that in Latin America there were some 1.4 million people infected with AIDS, while South and South East Asia combined accounted for 5.8 million people. These numbers are rounded up in the Caribbean, where at least 700,000 people had been infected as of 2000.

Scientists like Dr. Strecker, suggest that the fact that most of AIDS’s victims reside in Africa and Latin America is not a coincidence, as only 2 percent of the affected population resides in Europe. Apparently, the goal of creating a bioweapon such as the AIDS virus was to eliminate a great part of the Africans in an effort to reduce global population to just about 500 hundred million, down from some 7 billion. An example that helps reinforce this thesis is the Tuskegee Experiment. Conducted between 1932 and 1972, the Tuskegee Experiment, recruited some 400 black Americans in an effort to test the effects of syphilis in Macon County, Alabama. The United States Health Services never gave the subjects any clear information of what exactly would be put into their bodies, ans instead were drawn to the testing centers with promises that the injection would help them treat or cure problems like Anemia, or “bad blood”.

More recently, pharmaceutical companies like Merck have been found liable for the death of thousands of people as a consequence of taking drugs such as VIOX. In the latest battle of the people versus the pharmaceutical industry, groups of people around the world, but more specifically in Texas rose to denounce Merck’s intent to make a new vaccine -Gardasil- available to young women between the ages of 8 and 11 years old in order to -according to Merck- help prevent the Human Papiloma Virus or HPV. Parent groups denounced the measure taken by Texas governor Rick Perry who signed a document saying it was the law to take the vaccine. It would later be leaked to the public that Gardasil contains a live cancer virus something produced in a laboratory, which caused several dozen girls to bleed uncontrollably during the term the injections were taken and even after completing the multiple doses. Mothers of the girls appeared in national radio talk shows to testify of their experience and that of their daughters’.

According to Boyd E. Graves, who has studied the origins of the HIV virus for years, the history of the disease goes back at least 100 years. “The United States began a significant effort to investigate “causes” of epidemic diseases. In 1887, the effort was enhanced with the mandate of the U.S. “LABORATORY OF HYGIENE”. This lab was run by Dr. Joseph J. Kinyoun, a deep rooted-racist, who served the eugenics movement with dedication. In 1893, we strengthened the Federal Quarantine Act and suddenly there was an explosion of polio.” On his website, Graves continues with a chronological account of the way how an grand eugenics program grew from scratch. ” In 1945, we witnessed the greatest influx of foreign scientists in history into the U.S. biological program. Operation Paperclip will live in infamy as one of the darkest programs of a twisted parallel government fixated on genocide. In 1946, the United States Navy hired Dr. Earl Traub, a notorious racist biologist. A May appropriations hearing confirms the existence of a “secret” biological weapon. In 1948, we know that the United States confirmed the endorsement of “devising a scheme” in which to address the issue of overpopulation in certain racial groups. State Department’s George McKennan’s memo will forever illuminate the eugenics mendacity necessary for genocide of millions of innocent people.” Programs like the one orchestrated to exterminate much or all of the black population are true for other diseases such as Cancer, Polio, Influenza, and more recently Bird Flu.

Another piece of evidence that reinforces the fact that HIV AIDS as well as other diseases are man-made and not naturally born is the 1971 special virus flow chart, obtained by Graves in 1999. The chart was sent to him on May 15th, 2000 by Dr. Victoria Cargill of the National Institutes of Health. The chart shows how scientists proceeded when experimenting with new viruses. As I have seen it, it is a step by step guide to be followed and the way decisions are made according to the results obtained in every stage of the experiments. The chart indicates how to go through the process of selecting a candidate, how to proceed in order to determine whether a subject has experienced any immunological response to the virus (HIV), to confirming the effectiveness of controlled methods for introductions in critical trails.

It is estimated that if the HIV virus is not stopped within the next three decades, it will indeed achieve the objective it was meant for; it will completely eradicate the black population in Africa and other regions of the world. What is more incredible is that African governments consented in 1974 in Bucarest Romania to the use of the HIV virus on the population. According to Dr. Graves, there are at least 15,000 progress reports filed regarding the experiments with the HIV virus and the US government along with other European counterparts have spent $550 million dollars in the creation and spread of the HIV AIDS virus.

Consulted Materials include:

1. House of Numbers. Brent W. Leung

1. End Game: Blueprint for Global Enslavement. Alex E. Jones

2. “The Strecker Memorandum.” Distributed by The Strecker Group, Eagle Rock, CA., 1983.

3. “AIDS: United States Germs Warfare at its Best with Documents and Proof”. Jack Felder. 1989

4. “Who Murdered Africa.” William Campbell Douglas. M.D. 

5. “AIDS is Biological Warfare.” Tom Bearden.

6. “Smallpox vaccine triggered AIDS virus.”

7. “AIDS and the Doctors of Death: An Inquiry Into the Origin of the AIDS Epidemic.” Alan Cantwell.

8. “HIV infections up in Caribbean. The Plain Dealer.” 2000