Gardasil Vaccine rDNA Introduced at Coroner’s Inquest

Gardasil Vaccine rDNA Introduced at Coroner’s Inquest

Researchers such as Dr. Sin Hang Lee are finding contaminants in vaccines

Catherine J. Frompovich, Contributor
Activist Post

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, SaneVax, 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 SaneVax 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 SaneVax 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 SaneVax 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
SaneVax 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:
<blockquote class="tr_bq">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.</blockquote>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 withGardasil® ?
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.


Source:-
http://www.activistpost.com/2012/08/gardasil-vaccine-rdna-introduced-at.html