[SaneVax: Apparently the FDA has little, if any,  interest in real science, particularly when it comes to vaccine safety.   The following interview probably reveals only the tip of the iceberg when exposing problems with Gardasil that are ignored by the FDA. Since the FDA is  supposed to be responsible for ensuring the health and safety of the population of the United States–and other countries who rely upon FDA for medical science–those within the organization should be held personally accountable for their failures to act in the public’s best interest.

Part 1

Gardasil Vaccine rDNA Introduced at Coroner’s Inquest

By Catherine  J. Frompovich

Wellington, New Zealand.  According to testimony presented via international video link before a coroner’s inquest in Wellington, New Zealand, (August 9 NZ) by Dr. Sin Hang Lee (August 8 USA), a pathologist on the medical staff of Milford Hospital in the State of Connecticut, “residual HPV DNA fragments from the viral gene or plasmid injected with Gardasil®” have been found six months after that vaccination (series) was given to Jasmine Renata.  Ms. Renata, a teenager, died in her sleep of unknown and unexplained causes.  An autopsy was performed to determine cause of death.

—–

Interview With Norma Erickson, President, SANE VAX, Inc

Part 1 

Norma Erickson is President of Safe, Affordable, Necessary & Effective Vaccines and Vaccination Practices (SaneVax, Inc.), a vaccine safety advocacy group.  SaneVax became involved at the request of the late Jasmine Renata’s parents, who were seeking help understanding what happened to their lovely daughter following her death after experiencing numerous problems with the HPV vaccine Gardasil®.  ^[1]

This interview covers part of the ‘history’ involved in that unfortunate case.

Norma, can you please tell us the date of Jasmine’s death?

Jasmine died September 22, 2009.

Do you happen to know if Jasmine experienced any medical problems before her death?

Yes, beginning with warts and mood changes after her first injection; same thing after the second. The warts came back a third time after the last injection, mood and behavior changes, tingling sensations in her limbs, memory loss, tachycardia, chest pains and multiple other symptoms. The entire chronicle is here http://sanevax.org/jasmine-from-wellington/

How many Gardasil^® injections did Jasmine receive?  How far apart were the injections given?

Gardasil®, as you know, is a series of three injections.  The first injection was September 18, 2008; the second, November 18, 2008; and the third, March 17, 2009.

At any time were her parents suspicious of any reactions to the Gardasil®, vaccinations? If so, what were they? 

I have not spoken personally with Jasmine’s parents, as they have been working with an associate in New Zealand since shortly after their daughter’s death. Out of respect for their privacy, all personal contact is maintained through the person they had established a relationship with. That being said, Jasmine’s mother wrote her version of the events and allowed SaneVax to post it on our site in order to try and let other parents know the potential risks involved with HPV vaccinations. The story can be viewed here http://sanevax.org/gone-after-gardasil-jasmine-new-zealand/ .

How did SANE Vax become involved in this case?

Once information about Dr. Lee’s discovery of HPV rDNA fragments firmly attached to the aluminum adjuvant in multiple samples of Gardasil® circulated, SaneVax began to receive requests from parents of girls suffering severe reactions all over the world looking for a way their daughter’s blood could be tested for the contaminants. SaneVax had to turn them all down, because we knew Dr. Lee’s lab was not set up to work with blood samples and no protocol had been developed to try and detect HPV DNA particles attached to aluminum in human samples. No one knew if it would even be possible to detect such fragments.  Occasionally there would be some sort of special circumstance involved where I would forward an inquiry directly to Dr. Lee because the questions were beyond my field of expertise. The New Zealand advocate working with Renata’s parents posed many questions I could not answer with any degree of certainty, so I put her in direct contact with Dr. Lee.

I understand an autopsy took place.  What did that autopsy reveal?

The autopsy did not uncover any HPV DNA fragments. Quite the contrary, the autopsy ruled out all known causes of death.

So, why then, did a coroner’s inquest take place recently?

In New Zealand, when there is a death with no identifiable cause, it is routine for there to be an inquest.

Let’s back up a little. If you say SANE Vax was getting requests from around the world to have blood tested of young girls experiencing severe reactions to Gardasil®, how did this come to happen?

Originally, Dr. Lee tested 13 different Gardasil® vials from six different countries and four different manufacturing facilities, and all were found to be contaminated with HPV rDNA, firmly attached to the aluminum adjuvant.

Can you reveal the dates of Dr. Lee’s discovery?

The tests were done in June to August of 2011.

Did SANE Vax contact any health authorities, e.g., FDA?

As soon as Dr. Lee’s final report was turned in to SaneVax, we reported the situation to the FDA, September 2, 2011. Considering the Gardasil® issues came right on the heals of the Vioxx scandal, we saw no reason to report the issue to Merck. Furthermore, it is the FDA who is responsible for protecting the health and safety of medical consumers in the United States. Since that time, a couple more Gardasil® vials have been tested. I believe we are at 16 now, and all confirm residual HPV DNA.

I know we can’t divulge information regarding what took place at the inquest until the coroner releases it to the public, but from what you know of Dr. Lee’s research, can you please share with us what he found after his pathological examination, since he is under contract to SANE Vax and you are the owners of the research?

I can discuss it to the best of my ability.

Dr. Lee’s pathology report indicates that Gardasil® material was lodging in tissue and may have been causing health problems.  The fact that Gardasil® DNA fragments were suspended in post-mortem blood—and six months post vaccination—indicates there is pathology that HPV vaccine makers did not warn about on the vaccine package inserts as a contradiction.  How serious a problem is that for vaccine makers?

In my opinion, it poses a quite serious problem for two reasons. First, the manufacturer went to great lengths to remove all residual HPV DNA from the vaccine, including using a patented process to remove it from the vaccine. They assured regulatory agencies worldwide that there was no ‘viral DNA’ in the vaccine in order to obtain approval for marketing their product. Any way you slice it, HPV DNA is viral DNA – it need not be the complete virus to be viral DNA.

After we reported the presence of HPV DNA in Gardasil® to the FDA, FDA declared without presenting any supportive data that rDNA fragments are an acceptable excipient. The fact is the FDA does not know the physical condition of the HPV DNA or plasmid DNA in the vaccine. The physical condition of naked foreign DNA determines the fate of these DNA fragments and their pathophysiological effects in the human body.

Up to now, the vaccine industry always knew “The FDA specifically requires vaccine developers to show that VLPs [virus-like particles] do not encapsidate “specific” nucleic acid sequences from the expression system, and especially those encoding VLPs components.” (Valley-Omar’s paper)

Second, had Jasmine had wild (natural) HPV in her blood, it would not have lasted very long as the macrophages would have degraded it within a couple of days. Therefore, according to Dr. Lee:

“The finding of these foreign DNA fragments in the post-mortem samples six months after vaccination indicates that some of the residual DNA fragments from the viral gene or plasmid injected with Gardasil^® have been protected from degradation in the form of DNA-aluminum complexes in the macrophages; or via integration into the human genome. Undegraded viral and plasmid DNA fragments are known to activate macrophages, causing them to release tumor necrosis factor, a myocardial depressant which can induce lethal shock in animals and humans.”

Norma, could that tumor necrosis factor include cancer?  Are there other ‘unknowns’?

TNF [tumor necrosis factor] is but one possible byproduct of macrophage activation. To the best of my knowledge, it only affects the heart. Other cytokines also could theoretically be produced as a result of macrophage activation causing other problems – no one knows. Study in this area is relatively new.

No one knows the potential consequences of these foreign DNA fragments remaining in the human body. Can they cause cancer? Can they cause autoimmune disorders? Can they cause birth defects? Can they cause death? No one knows – that is a HUGE problem, in my opinion.

Do you think AAHS [amorphous aluminum hydroxyphosphate sulfate] in Gardasil^® can be the primary contributing factor to so many deaths and adverse reactions in young girls who were vaccinated with Gardasil^® ?   Please elaborate.

Personally, having looked at the results of the clinical trials where the vaccine was tested against the AAHS as a control, I believe it is a strong possibility that AAHS is a contributing factor. The reason being the adverse events during the trials were somewhat evenly distributed between the two groups. Unfortunately, over 70% of all trial participants experienced a ‘new medical condition’ during the trials – which, by the way, is the CDC’s definition of an adverse event.

How very interesting!  And, of course, that does not appear on vaccine package inserts, does it? 

The only thing quoted in package inserts or advertising is Gardasil^® is safe and effective. It does not seem to matter what the truth is, i.e., the vaccine appeared to be no more dangerous than the adjuvant during clinical trials. Remember that even this may be misleading, as no one knows the long-term effects of the HPV DNA particles. The real experiment is being conducted on young people around the world as we speak.

What did Dr. Lee’s pathology report state regarding that connection?

Dr. Lee was not looking for aluminum damage or exposure. He was simply attempting to discover whether or not the HPV DNA fragments found in Gardasil^® were also present in autopsy samples.

According to Dr. Lee, the HPV DNA fragments in the vaccine were firmly bound to the amorphous aluminum hydroxyphosphate sulfate (AAHS) particles that are used as an adjuvant in Gardasil^® formulation.  The post-mortem finding obviously indicates an apparent unknown role AAHS in Gardasil^® plays in the body’s retention of HPV DNA particles, especially since a relatively high amount of AAHS is administered with each vaccination.  What should the U.S. CDC and FDA do in view of these findings?

Ideally, these agencies would rescind Gardasil^® approval until such time as independent—not Big Pharma—laboratory analysis could prove the residual HPV DNA attached to an aluminum compound poses no risk to medical consumers.

Well, isn’t that part of the problem with vaccines, e.g., the rush to get vaccines certified for human use often with a rush to judgment and sometimes-flawed science?

Yes, at the very least, the CDC/FDA should provide autopsy samples from all deaths subsequent to Gardasil^®vaccinations to independent laboratories with suitable technology to investigate the situation further. Anything less is a betrayal of the public trust.

I think this is where we can end Part 1 of this interview. In Part 2 we will address as much as we can about Dr. Lee’s research.

Bombshell Interview Reveals DNA Fragments Discovered 6 Months After Vaccination

By Catherine J. Frompovich

Interview With

Norma Erickson, President, S.A.N.E. VAX, Inc. 

Gardasil Vaccine rDNA Introduced at Coroner’s Inquest 

Part 2 

Sin Hang Lee, MD, is a medical practitioner historically qualified to practice medicine in the People’s Republic of China, the District of Columbia, New York State, and the State of Connecticut in the USA, plus in Canada and British Commonwealth countries via his registration with the General Medical Council of the UK.  Currently Dr. Lee holds a medical license in the State ofConnecticut,USA.

Dr. Lee has staff privileges at the Milford Hospital in Milford,Connecticut.  He was certified by the American Board of Pathology in anatomical pathology (1966); certified in general pathology by the Royal College of Physicians and Surgeons of Canada (1966); and granted the F.R.C.P. degree by the Royal College of Physicians and Surgeons of Canada (1966).  Dr. Lee has practiced diagnostic pathology in Canada and the USA continuously since 1966 with a special interest in developing new technologies in laboratory medicine.  His most recent research is the use of low temperature (LoTemp®) polymerase chain reaction (PCR) and direct automated Sanger DNA sequencing to increase the sensitivity and specificity of the molecular diagnosis of infectious diseases.

Using Dr. Lee’s new methods, PCR can detect HPV L1 gene DNA bound to nanoparticles; it can detect HPV L1 gene DNA of vaccine origin present in human blood and tissue samples.

Norma, given the above professional bio about Dr. Lee, one has to assume he is more than qualified to discuss his findings with regard to the Jasmine Renata case inNew Zealand.  I understand Dr. Lee was one of numerous experts and witnesses to testify at the recent (August 9, 2012) two-day inquest held to determine the cause of death, which could not be determined officially by autopsy.  This case has gathered local interest and coverage.  I understand the New Zealandpress covered the event in real-time and reported on it.  Here are two links to that coverage.

The Dominion Post  http://www.stuff.co.nz/dominion-post/news/7437620/Teens-brain-tissue-sent-for-examination

Otago Daily Times http://www.odt.co.nz/news/national/220882/biological-plausibility-vaccine-caused-death

Since we cannot discuss the inquest until the coroner releases that information, let’s talk about some of what we know.  Dr. Lee tested 16 samples of Gardasil^® in use from 9 countries, each with a different lot number. The lot numbers of the 5 New Zealand samples, the cities of origin and the HPV genotypes of the L1 gene DNA found in each sample are listed below: 

There seems to be a potential problem that falls back on to the Renata case insofar as Dr. Lee’s findings in Jasmine’s blood and spleen tissue and the above findings.  Can you please tell us about that?

Yes, Catherine, there are multiple potential problems with discovering HPV-16 L1 DNA in Jasmine’s samples. We must emphasize that what was discovered in the Gardasil® vaccine and in Jasmine’s samples are viral DNA fragments, not the infective wild viruses.

First, HPV infection is confined to epithelium. This virus does not survive in the blood or in other organs of a healthy woman.  Any naked HPV DNA fragments in the circulating blood would be degraded by serum or intracellular DNA nucleases (enzymes) if these fragments are taken up by the macrophages (a component of the white blood cells), and eliminated from the body in 24-48 hours.

Since the HPV-16 L1 gene DNA fragments were discovered 6 months after Jasmine’s last Gardasil^® vaccination, we have to assume these HPV DNA fragments were either protected by being firmly bound to the aluminum adjuvant, or by integrating themselves into the human genome through poorly understood mechanisms.

Didn’t Jasmine’s mother contact Dr. Lee after she had read that the U.S. FDA announced that the Gardasil® vaccine contained residues of HPV L1 gene DNA?

Jasmine’s parents made contact with us after the discovery of genetically engineered HPV DNA in Gardasil® through an associate we work with inNew Zealand. They were then put in direct contact with Dr. Lee because of his expertise.

I think our readers ought to know that the FDA affirmed Gardasil® samples do contain HPV L1 gene DNA fragments. 

That can be confirmed on FDA’s website    http://www.fda.gov/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm276859.htm   

Wasn’t that an ‘after-the-fact’ FDA announcement to its certifying that Gardasil® was safe and effective, despite it being bound to insoluble adjuvant AAHS particles?  How could that have slipped by the certifying process?  I guess that does not appear on the vaccine package insert, does it?

The webpage you refer to was a public response to the SaneVax letter which informed the FDA of the contaminants Dr. Lee had discovered. Anyone reading the FDA’s announcement should note there are absolutely no scientific references to back up the claims, and I quote, “The presence of these DNA fragments is expected, is not a risk to vaccine recipients, and is not a safety factor.”

In stark contrast, readers can examine our original letter informing the FDA of this potential health risk here – http://sanevax.org/sane-vax-to-fda-recombinant-hpv-dna-found-in-multiple-samples-of-gardasil/

Instead of conducting further investigation into our discoveries, including the finding of HPV DNA fragments firmly bound to the insoluble AAHS adjuvant, the FDA issued a blanket statement as to the vaccine’s safety.

AAHS is listed as an adjuvant on the package insert. But a molecular complex of HPV DNA or plasmid DNA fragments firmly bound to the AAHS particles (probably through a chemical reaction) are not.

Don’t those insoluble adjuvant AAHS [amorphous aluminum hydroxyphosphate sulfate] particles and the HPV L1 gene DNA encourage cytokine production, which apparently is not listed on the vaccine package insert? 

AAHS is Merck’s proprietary mineral-based insoluble adjuvant with a very high binding capacity for HPV VLPs, the active major capsid protein antigen in Gardasil®. The vaccine manufacturer and the FDA might have known there would be residual HPV DNA and plasmid DNA in the Gardasil® vaccine, if there is evidence to support that claim.

However, they did not know (or, if they knew, did not disclose) the physical condition of these naked viral (HPV) and bacterial (plasmid) DNA in Gardasil®. For example, these DNA fragments could be in the aqueous phase (dissolved in water), encapsulated in the VLPs, or bound to the AAHS by electrostatic attraction or an irreversible chemical reaction between the aluminum in the AAHS and the phosphate backbone of the DNA molecules.

In his testimony, Dr. Lee presented experimental evidence to show that DNA/AAHS complexes may constitute a new chemical compound with unknown effects. As all AAHS nanoparticles are designed to be phagocytized by tissue macrophages after intramuscular injection, any foreign viral and/or plasmid DNA present would be carried into the cytoplasm of the macrophages along with the AAHS nanoparticles. Once in the cytoplasm, these foreign DNA fragments, protected from degradation, may act as long-acting stimulators to activate the macrophages to signal the production of cytokines, such as tumor necrosis factor (TNF).

TNF is a known myocardial depressant capable of causing hypotension and lethal shock in animals and in humans, as well as other symptoms commonly reported by the girls vaccinated with Gardasil^®.

Persistence of foreign DNA fragments in the cells increases the chance of integration of the foreign DNA into the human genome through poorly understood mechanisms, thus increasing the risk of gene mutations and cancer.

Should MDs who administer Gardasil® be aware of that key omission on package inserts because of the potentialities of what can happen to vaccinees, e.g., tumor necrosis factor, even sudden death syndrome from myocardial dysfunction or as a result of maldistribution of peripheral blood flow?

It is not standard practice to warn physicians or medical consumers of unproven scientific theories. To date, there has been no research in the area of the risks of foreign DNA being attached to aluminum particles included in vaccines. The research to discover the real risks just has not been done.

That being said, those who administer Gardasil® should be made aware of the fact that severe adverse reactions occur at a higher rate than deaths from cervical cancer in most developed countries, the United States being one. [Reference: http://informahealthcare.com/doi/abs/10.3109/07853890.2011.645353]

What is the tumor necrosis factor?

TNF is a cytokine primarily secreted by macrophages (white blood cells). This cytokine is involved in the regulation of a wide spectrum of biological processes including cell proliferation, differentiation, apoptosis, lipid metabolism, and coagulation. It is one of the cytokines that have been implicated in a variety of diseases, including autoimmune disorders/diseases, insulin resistance, and cancer. [Reference: http://www.ncbi.nlm.nih.gov/gene/7124]

Isn’t the tumor necrosis factor (TNF) a recognized myocardial depressant?  Isn’t TNF known to cause the release of cytokines?

TNF is one of the cytokines, which may be produced when either naked viral or bacterial DNA activates the macrophages. Yes, according to Dr. Lee, “It is a known myocardial depressant capable of inducing lethal shock in animals and in humans.”

[References: Parrillo JE, etal. J Clin Invest. 1985;76:1539-1553; Kumar A, etal. Am J Physiol Regul Interg Comp Physiol. 2007;292-:R1900-6; Cauweis A, etal. Immunity. 2000;13:223-231; Cauweis A, etal. Arch Biochem Biophys. 2007;462:132-139;  Cauweis A, etal. Nat Immunol. 2003;4:387-393.]

One may also consider since the medical profession currently uses TNF-blockers to treat inflammatory conditions such as Crohn’s disease, lupus and rheumatoid arthritis, that overproduction of TNF may be a precursor to these and possibly other autoimmune disorders. [References: http://www.medterms.com/script/main/art.asp?articlekey=25458 http://www.arthritis.org/tnf-inhibitor-b-cell.php]

If I’m not mistaken, don’t HPV L1 gene DNA residues left in Gardasil® bind to cationic AAHS [amorphous aluminum hydroxyphosphate sulfate] nanoparticles?

Yes, at pH 6.0-6.5, AAHS in the Gardasil® vaccine carries a positive charge and the DNA a negative charge. Therefore, there is an electrostatic attraction between the two. But as Dr. Lee testified at the Jasmine inquest, a highly stable, perhaps irreversible, new chemical compound of the cationic aluminum bound to the phosphate backbone of the DNA molecule may have been created in the Gardasil® vaccine. The toxicity of the DNA/AAHS complexes is totally unknown.

How much AAHS adjuvant is there in each Gardasil® 0.5ml dose?

There are 225 mcg of AAHS in each of the three recommended doses to complete the series.

Aren’t the proteins used as antigens in Gardasil® manufactured in yeast cells using genetic engineering?  That’s not in the public knowledge, is it—especially genetic engineering manufacturing in association with the use of aluminum-based nanoparticles as adjuvant? What type of impact, if any, would that have in cytokine production? 

Yes, the HPV L1 protein virus-like particles (VLP’s) used as antigens in Gardasil® are manufactured with yeast cultures using genetic engineering. The method by which they were produced was explained, but in my opinion, the general public did not connect the explanation of the concept with genetic engineering. It is my understanding that any foreign (meaning non-human) DNA remaining in the vaccine, whether it be from HPV, bacteria, yeast, or any other ingredient used in the manufacturing process could pose unknown health risks. Viral DNA and bacterial DNA fragments firmly bound to aluminum salts are more of a concern than yeast DNA, particularly when it comes to the potential of causing lethal shock.

For those who doubt the HPV L1 gene DNA findings, what are the odds that prove that Jasmine’s samples were accurate and beyond a reasonable doubt?

As Dr. Lee testified, his findings are validated by DNA sequencing, the gold standard for HPV DNA detection and genotyping. A few split samples, which Dr. Lee has tested in Connecticut, are being retained in Auckland Hospital. Other interested scientists may reproduce Dr. Lee’s test results by testing those retained samples, which can leave New Zealand only with the Coroner’s authorization.

Macrophages—white blood cells—get involved.  Can you explain what transpires in the body that implicates Gardasil®?

Honestly, I cannot explain what happens in the body. What we have here is HPV L-1 gene DNA in the vaccine firmly attached to the aluminum adjuvant, a DNA/mineral complex which was not expected. We have HPV-16 L-1 gene DNA in the macrophages of post-mortem blood and spleen samples, a finding which was not expected in a healthy woman. There are only two ways HPV DNA could have remained in post-mortem tissue – either it was protected from normal degradation by being firmly bound to the cationic aluminum; or it had integrated into the human genome. Either one poses serious potential consequences that need to be defined and disclosed. It is the job of the FDA/CDC/NCI and any other federal agency responsible for protecting the health and welfare of the American public to conduct the necessary studies to answer the questions about potential health risks.

If your readers would like to learn about the potential consequences, I would suggest they search for ‘macrophage activation syndrome.’ They will find over 365,000 sites linking to the latest scientific data.

If all Gardasil® samples Dr. Lee tested were positive, what are the implications regarding genetic engineering in any vaccine manufacturing? 

I would personally think it would bring any genetically engineered vaccine under scrutiny for the same potential risks.

That information about Gardasil® impacting white blood cells and tumor necrosis factor does not appear on the vaccine package insert.  What do you have to say about that? 

It would not appear on the package insert, as it was just recently discovered. However, that does not absolve the FDA of at least some culpability in the matter. When the FDA was informed of the contaminating HPV DNA, they did an immediate about-face from ‘no viral DNA’ to ‘it was known and expected.’

If indeed, it was ‘known and expected,’ medical consumers deserve the answers to the following:

• Exactly when did Merck inform the FDA there is viral DNA in Gardasil®? In a letter dated April 19, 2006, Merck emphatically stated Gardasil® ‘contains no viral DNA.
• If Merck did report this to the FDA, what did the report state about the physical condition of the HPV DNA fragments in the final product? Were they in the aqueous phase of the vaccine suspension? Were they encapsulated in the VLP’s? Were they bound to AAHS nanoparticles? If so, how were they bound? (Naked foreign DNA in different physical conditions may have different pathophysiologic impacts on the human body.)
• Did Merck report the presence of plasmid DNA in addition to the HPV DNA? (Plasmid is DNA from bacterial origin and is attached to the HPV L1 gene for production of the vaccine protein. It may be expected to be present together with the HPV DNA in the vaccine.)
• If Merck knew the HPV DNA was bound to AAHS to form DNA/AAHS complexes, where are the reports from the studies they must have performed on the pathophysiologic implications of using these complexes?

Now here’s something that should be a ‘clincher’, I think. I understand HPV DNA was reported in the plasma of patients with invasive cervical cancer, which was known to be the source of HPV DNA in plasma.  Furthermore, HPV DNA was not detected in plasma samples of patients who did not have cervical cancer.  Jasmine did not have cervical cancer, as determined by autopsy. Therefore, she/her body should not have any HPV DNA from a cancer.  What do you have to say to that? 

As stated previously, there are very few conditions under which HPV DNA would remain in a person’s blood and spleen long enough to be detected. This is one such circumstance. [References: Pornthanakasem W, etal. BMC Cancer. 2001;1:2; Shimada T, etal. Jpn J Clin Oncol. 2010;40:420-424]

We’ve been talking about HPV L1 gene DNA in blood and spleen samples.  Were any found elsewhere in Jasmine’s tissues? 

We have learned via a report fromNew Zealand that:

 “Neuroscientist Professor Christopher Shaw of the Universityof Columbia inVancouver told the inquest via video-link today that he was sent Ms Renata’s brain tissue to test.

He said there was aluminum in all the samples he tested and there were some abnormalities in the samples.

“The human papillomavirus (HPV16) was found in her brain, which could have only got there through the vaccine.” Prof Shaw said.

http://www.odt.co.nz/news/national/220882/biological-plausibility-vaccine-caused-death

Do you think the FDA should be looking for a cause-effect link between HPV L1 gene DNA-activated macrophages and lethal shock? 

Of course they should be looking! At the very least, they should be hunting down samples from every unexplained death after Gardasil® and sponsoring independent studies to determine if HPV L-1 gene DNA is present in others. They should also be looking at those reporting serious adverse events after Gardasil® for the same DNA.

As it stands, the FDA is not living up to their mission statement, which states:

“FDA is responsible for protecting the public health by assuring the safety, efficacy and security of human and veterinary drugs, biological products, medical devices, our nation’s food supply, cosmetics, and products that emit radiation.

“FDA is also responsible for advancing the public health by helping to speed innovations that make medicines more effective, safer, and more affordable and by helping the public get the accurate, science-based information they need to use medicines and foods to maintain and improve their health…..” [Reference: http://www.fda.gov/aboutfda/whatwedo/default.htm]

Medical consumers have trusted the FDA to do exactly that – protect the public health and help them get accurate, science-based information – these trusting medical consumers have been betrayed.

Norma, thank you so very much for this interview.  I appreciate your cooperation in helping healthcare consumers understand issues authorities apparently don’t want to discuss.

###

[Note: This interview was originally posted as a two part series on VacTruth.com via the following links – http://vactruth.com/2012/08/09/gardasil-rdna-coroners-inquest/ and – http://vactruth.com/2012/08/16/rdna-fragments-after-vaccination/. They were posted here with the kind permission of the author Catherine Frompovich. the SaneVax team wishes to express our sincere appreciation to the staff of VacTruth and Catherine for their their ongoing efforts to reveal the truth.]