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HPV Vaccines are a Betrayal of the Public Trust

By NORMA ERICKSON | SANEVAX | MARCH 27, 2013

Last week, multiple news articles reported 44% of American parents refusing Gardasil or Cervarix for their children. Between 2008 and 2010, the percentage of parents concerned about the safety of these two vaccines nearly quadrupled. As of 2010, only 32% of eligible girls were vaccinated against HPV. What is wrong with this picture?

Excerpts from national news sources, March 18-22, 2013:

  • USA Today The percentage of parents who say they won’t have their teen daughters vaccinated against the human papillomavirus increases, even though physicians increasingly recommend the vaccinations. Concerns about safety and side effects for the human papillomavirus (HPV) vaccine have increased among parents: 16% cited these fears as the main reason they did not have their daughters vaccinated in 2010, up from 5% in 2008…
  • Medpage Today Parents increasingly say they are worried about the safety of the human papillomavirus (HPV) vaccine and don’t intend to vaccinate their teen daughters… But there is no similar pattern for two other vaccines aimed at adolescents…
  • CNN Health Concerns of mothers and fathers about the safety of the HPV vaccine grew each year, from 4.5% in 2008 to 16.4% in 2010… The number of parents who said they would not vaccinate their children for HPV increased from 38.9% in 2008 to 43.9% in 2010. The main concern was safety.
  • CBS News One of the main reasons parents said they didn’t want their children vaccinated against HPV was because of safety concerns.
  • Bloomberg The number of girls who received either injection (Gardasil or Cervarix) rose to about one-third in 2010 from 16 percent in 2008…
  • FiercePharma A growing share of U.S. parents say they won’t vaccinate their daughters… And that leaves Merck’s Gardasil and GSK’s Cervarix with a shrinking market.
  • The New York Timessuggesting, the need for interventions beyond clinical recommendations like possibly ‘state and federally designed social marketing campaigns.’… Without brushing aside the need to address safety concerns, the increasing rates of HPV vaccine refusal suggest that widespread vaccination will require more than marketing campaigns. Medical professionals need to look for ways to tell a better story to parents and teens about HPV, vaccination and cancer. (emphasis added)

Taxpayer funded social marketing campaigns? Look for ways to ‘tell a better story’ to parents? Who are these people kidding? What happened to investigative journalism? What happened to fact-finding? What happened to fair and balanced journalism?

Has no one considered the possibility that the 43.9% of parents refusing this particular vaccine might have some valid concerns? When will people realize there is a huge difference between ‘increasingly concerned about the safety’ and ‘increasingly aware of the potential risks’? After all, this would not be the first time a prescription medication approved by the FDA as ‘safe and effective’ turned out to be nothing of the sort. Will HPV vaccines be next?

HPV vaccination programs worldwide are based on two assumptions. First, HPV vaccines will prevent cervical cancer and save lives. Second, HPV vaccines will pose no risk of serious side effects. Therefore, it would make sense to vaccinate as many pre-adolescent girls as possible to reduce the worldwide burden of cervical cancer. What happens if both of these assumptions are not based on factual evidence?[1]

Medical Consumers Want to Know:

  1. Since HPV vaccines have never been shown to prevent cervical cancer, why are they being promoted as cervical cancer vaccines?1
  2. Since the majority of HPV infections and a great proportion of abnormal lesions associated with cervical cancer development clear spontaneously without medical treatment, how can these factors be used as ‘end-points’ during clinical trials to reliably predict the number of cervical cancer cases that could be prevented by HPV vaccines?1
  3. How can the clinical trials make an accurate estimate of the risk associated with HPV-vaccines if they are methodologically biased to produce false negatives?1
  4. Why are HPV vaccines marketed so aggressively in developed countries, when 85.5% of annual cervical cancer cases and 87.9% of annual cervical cancer deaths occur in developing countries?[2]
  5. How can passive adverse event monitoring systems (voluntary reporting with no penalty for failure to report), such as those used by most vaccine surveillance systems world-wide, allow the medical regulatory agencies to make accurate estimates on the real frequency of HPV-vaccine related adverse reactions?
  6. How can accurate estimates of the real frequency of HPV-vaccine related adverse reactions be made if appropriate follow-up and thorough investigations of suspected vaccine reactions are not conducted?

The FDA granted Merck’s HPV vaccine, Gardasil, fast track approval in June of 2006, despite the fact that this HPV vaccine failed to meet the FDA criteria for fast track approval.[3] FDA approval of GSK’s HPV vaccine, Cervarix, followed shortly after in January 2007.

According to The New York Times, the CDC Advisory Committee on Immunization Practices recommended adding HPV vaccines to the immunization schedule in the U.S. despite the fact that 64% of the advisory committee members had potential conflicts of interest which were either never disclosed or left unresolved at the time they voted. 3% of the members actually voted on matters they had been barred from considering by ethics officers. News like this certainly does little to enhance the level of public trust.

Is it possible for the FDA to objectively monitor the safety and efficacy of HPV vaccines? One has to wonder since Congress tightened the rules on outside consulting after similarly undisclosed conflicts of interest were discovered within advisory committees at the FDA.

As if this is not enough, the United States Department of Health and Human Services, via the National Institutes of Health, Office of Technology Transfer receives royalties on each HPV vaccine sold worldwide. This happens because technologies used in the production of HPV vaccines were developed at NIH and subsequently patented by them. For three of the last five years, HPV vaccines based on recombinant papillomavirus capsid proteins have ranked #1 based on royalties from product sales.[4]

Marketing Gardasil to the public under these circumstances is a typical case of unconstrained government self-dealing. The major patent holder (National Cancer Institute/NCI), the regulator (FDA) and the vaccination policy maker (CDC) are all divisions of the Department of Health and Human Services (DHHS). These self-dealings typically benefit some administrators, not the government or tax payers.  For example, Dr. Julie Gerberding, as the Director of the CDC, approved the use of Gardasil for cervical cancer prevention as a public health policy is now the president of Merck’s Vaccine division promoting the sales of Gardasil.

How much revenue is generated for the NIH from international sales of HPV vaccines? In November 2010, Dr. Eric Suba submitted a Freedom of Information Request to the Office of Government Information Services to discover the amount. It seems the financial details of the partnership between the NIH, Merck and GlaxoSmithKline are exempt from disclosure. (Read the response he received here.) Apparently, transparency in government does not apply to the top 20 revenue producing patent(s) developed at taxpayer expense. Why is the public not allowed to share in celebrating the success of products they financed?

Three Strikes for Gardasil?

  1. September 2011: Recombinant HPV DNA L1 protein fragments, possibly attached to the aluminum adjuvant, were discovered in 100% of Gardasil samples tested. There was no subsequent investigation. The FDA simply declared the ‘expected’ presence of residual DNA is not a safety factor. No documentation was provided. The fact that HPV vaccines were approved by governments worldwide based on manufacturers’ assertions that the vaccines contained ‘no viral DNA’ was completely ignored.[5], [6] The possibility of recombinant HPV DNA fragments being attached to aluminum adjuvant particles was also ignored.
  2. August 2012: One of the antigens used in Gardasil was discovered in central nervous system samples from two girls who died after being vaccinated with Gardasil. No cause of death was identified upon autopsy in either case.[7] HPV-16 L1 gene DNA fragments of vaccine origin apparently attached to aluminum adjuvant particles were also discovered in post mortem blood and spleen samples of a girl who died 6 months after Gardasil injections.[8], [9]
  3. February 2013: It was discovered that the naked HPV 16 L1 gene fragments bound to aluminum particles by ligand exchange in Gardasil have acquired a non-B conformation. This conformational change may have stabilized the HPV 16 gene fragments in Gardasil preventing their normal enzymatic degradation in vaccine recipients.[10], [11] Non-B DNA conformations and their relationship to diseases has been studied since the 1960’s. Based on current scientific knowledge, the human genetic consequences of these non-B DNA structures are approximately 20 neurological diseases, approximately 50 genomic disorders and several psychiatric diseases.[12], [13] The impact of injected foreign non-B DNA on human health is totally unknown.

Why have none of these discoveries sparked a single investigation in any country? Why is no one concerned when genetically modified viral DNA fragments are found in vaccines that are reported to have no viral DNA? Why is no one worried about those viral DNA fragments being attached to aluminum (a known toxin) possibly creating a new chemical compound of unknown toxicity? Why are no red flags raised when those viral DNA fragments attached to aluminum acquire a non-B conformation – something known to be associated with multiple debilitating diseases? Anyone with an ounce of common sense should demand to know why those charged with approval, recommendation and safety monitoring of these vaccines appear to be utterly unconcerned about the future health implications of any one of these discoveries, much less all three of them.

What kind of ‘expert’ advice is being given to YOUR government health officials?

Israel’s Advisory Committee on Infectious Diseases and Inoculations held a teleconference on 30 January 2013, to discuss the proposed introduction of HPV vaccines into the country’s school inoculation program among other issues. The official transcript of that meeting, dated 11 February 2013, provides some interesting insights for medical consumers who question HPV vaccine safety.

Ron Dagan, MD, is Professor of Pediatrics and Infectious Diseases at the Ben-Gurion University of the Negev in Beer-Sheva, Israel, and Director of the Pediatric Infectious Disease Unit at the Soroka University Medical Center, also in Beer-Sheva. An active researcher and international lecturer, Dr. Dagan’s work focuses on new conjugate vaccines. His expert advice to Israel’s Advisory Committee regarding potential HPV vaccine implementation is as follows (translation provided-emphasis added):

We are dealing with injections, some of which given in 3 [separate] doses, which are delivered to teenage girls. Many side effects are to be expected. During the week following the vaccine delivery of the injections many serious events which are not related/linked to the vaccination are expected: fainting, deaths and convulsions/fits. This needs to be taken into account. Even if it is not rational, if these events happen in class they may damage the general perception/status of the vaccinations. This is happening all over the world all the time. We have already dealt with a similar issue in relation to the delivery of MMT with TD and Polio and we have accepted the nurse’s proposal to split these between grades 1 and 2. The nurses are suitable to make recommendations to the committee in relation to this issue. In relation to the side effects, we need to be prepared in advance and not simply react after the fact. I propose we consult with the English representatives as to how they’ve gone about this. We must prepare for the delivery of the new vaccine. The nurses need to know they are going about this in the way they are most comfortable with (/have the most control over/familiarity with).

If this is an example of the expert advice vaccination programs are based on, it’s no wonder medical consumers are questioning HPV vaccine safety, efficacy and need. Many side effects are to be expected? Fainting, deaths, convulsions and fits occurring during the week following vaccination – yet not related to the vaccine? Preparing in advance for side effects? Consulting with other countries to see how they handled the problem? Are countries around the world being offered similar expert advice?

So, what will it take to solve the HPV vaccine uptake problem?

Parental concerns about HPV vaccine safety are not going to go away in response to social media campaigns. Teaching medical professionals to ‘tell a better story’ is not going to make parents change their mind about Gardasil, Cervarix, or any future HPV vaccine. Platitudes and unsubstantiated reassurances are no longer sufficient.

The time has come for government health authorities to make HPV vaccine manufacturers prove their claims or pull their products from the market. Medical consumers want scientifically proven facts – Safe, Affordable, Necessary and Effective – nothing less is acceptable.

References:

[2] WHO/ICO Information Centre on HPV and Cervical Cancer (HPV Information Centre). Human Papillomavirus and Related Cancers in World. Summary Report 2010.

[3] Too fast or not too fast: the FDA’s approval of Merck’s HPV vaccine Gardasil. Tomljenovic/Shaw 2012

[4] Top 20 Commercially Successful Inventions, NIH

[5] SaneVax to FDA: Recombinant HPV DNA found in multiple samples of Gardasil

[6] Detection of human papillomavirus (HPV) L1 gene DNA possibly bound to particulate aluminum adjuvant in the HPV vaccine Gardasil® Lee 2012

[7] Death after Quadrivalent Human Papillomavirus (HPV) Vaccination: Causal or Coincidental? Tomljenovic/Shaw 2012

[8] Detection of human papillomavirus L1 gene DNA fragments in postmortem blood and spleen after Gardasil® vaccination—A case report Lee 2012

[9] Death after Quadrivalent Human Papillomavirus (HPV) Vaccination: Causal or Coincidental? Tomljenovic/Shaw 2012

[10] Topological conformational changes of human papillomavirus (HPV) DNA bound to an insoluble aluminum salt—A study by low temperature PCR, Lee 2013

[11] Gardasil: New Study Brings More Safety Questions to Light, Erickson 2013

[12] Non-B DNA conformations, mutagenesis, and disease, Wells 2007

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Third world people reject Bill Gates’ charitable vaccinations

By CHRISTINA ENGLAND | VACTRUTH | FEBRUARY 27, 2013

In January 2013,  Bill Gates told the world in an interview that he had no need for money and that he believed the global vaccination program was God’s work. [1] “It’s not going to stop us succeeding,” says Gates. “It does force us to sit down with the Pakistan government to renew their commitments, see what they’re going to do in security and make changes to protect the women who are doing God’s work and getting out to these children and delivering the vaccine.”

His words came after several vaccine workers administering the polio vaccination in Pakistan were shot dead in January. [2]

It appears that although Gates wants to carry on with what he calls ‘God’s work,’ people living in the third world are beginning to make their feelings abundantly clear. It appears that they don’t want his vaccines or his charity, as more shootings were reported in Nigeria.

On February 8, 2013, The Guardian reported that at least nine health workers administering the polio vaccinations in Nigeria were shot dead by gunmen thought to belong to radical an Islamist sect. The Guardian wrote:

“The killings drew comparisons with a series of incidents in Pakistan last December where five female polio vaccinators were gunned down, apparently by Islamist militants. It also signalled a fresh wave of hostility towards immunisation drives in Nigeria, where some clerics have claimed the vaccines are part of a western plot to sterilise young girls and eliminate the Muslim population.” [3]

DO YOU KNOW WHAT’S IN THAT NEEDLE?

They are right to be suspicious because it would not be the first time that vaccines were given with the intention of sterilizing women in the third world. In 1995, many third world countries were given a tetanus vaccine containing a birth control drug by the World Health Organization.

An organization known as The Comite became suspicious of the protocols surrounding the vaccines and obtained several vials for testing. It was discovered that some of the vials contained human chorionic gonadotrophin (hCG), a naturally occurring hormone essential for maintaining a pregnancy.

However, when combined with a tetanus toxoid carrier, this vaccine essentially causes a woman’s body to produce antibodies against pregnancy, forcing her body to abort her unborn baby, as reported by ThinkTwice Global Vaccine Institute:

“In nature the hCG hormone alerts the woman’s body that she is pregnant and causes the release of other hormones to prepare the uterine lining for the implantation of the fertilized egg. The rapid rise in hCG levels after conception makes it an excellent marker for confirmation of pregnancy: when a woman takes a pregnancy test she is not tested for the pregnancy itself, but for the elevated presence of hCG.

However, when introduced into the body coupled with a tetanus toxoid carrier, antibodies will be formed not only against tetanus but also against hCG. In this case the body fails to recognize hCG as a friend and will produce anti-hCG antibodies. The antibodies will attack subsequent pregnancies by killing the hCG which naturally sustains a pregnancy; when a woman has sufficient anti-hCG antibodies in her system, she is rendered incapable of maintaining a pregnancy.” [4]

Curiously, no men, boys or babies were vaccinated during the program. The only people vaccinated with this particular vaccine were women aged between 15 and 45. Was it a coincidence that these vaccines were only given to women of childbearing age? After all, anyone can contract tetanus, can’t they?

THE ADVERSE EVENT YOU MIGHT NOT EXPECT

Polio vaccine workers are not the only health workers who have been attacked during the last few months. In December 2012, La Voix reported that parents of vaccine-damaged children in Chad, Northern Africa, took out their anger and frustration by torching a car belonging to a hospital worker. [5]

VacTruth has since been informed by Chadian contacts that the people of Chad are boycotting all vaccinations, while the parents of the vaccine damaged children stoned the school’s headmaster who had forced pupils to take the MenAfriVac Meningitis A vaccine. The parents have since announced that they have no choice but to take government and its international organizations to court.

This is probably because whether Gates believes he is doing ‘God’s work’ or not, dumping severely vaccine damaged children in a remote village in Africa without a doctor on site is almost certainly not God’s work and this is exactly what Gates has allowed to happen to the children adversely affected by the MenAfriVac Meningitis A vaccine.

Over the last few months I have written four articles covering recent events in Chad, Northern Africa, where 106 children became ill after receiving the meningitis vaccine, 40 of which were left paralyzed and suffering from convulsions. [6,7,8,9]

This week, VacTruth received word from a Chadian contact that said:

“Last night the Chadian minister of health evacuated all children paralyzed from MenAfriVac meningitis A vaccine, including very ill children, to Faya. I have just spoken to one person, who told me that seven girls and a boy are seriously ill with convulsions.

Please, help us. This forced evacuation of very ill and paralyzed children on a military plan, to a destination where there is not even basic medical personnel and equipment, is deliberately sending vulnerable children to a place where they are likely to die.”

Faya is a small town surrounded by desert at least 100 miles away from the children’s home village of Gouro. This is extremely worrying, especially after VacTruth received several medical records confirming that these children did indeed suffer vaccine injuries.

MEDICAL RECORDS AS EVIDENCE

Over the past three months, members of the community of Gouro have reached out to VacTruth with desperate pleas for assistance as they helplessly watch their children suffer. We received a copy of one of the children’s medical records from their parent, which was written in French and translated on our behalf by Desiree Rover, an activist and avid campaigner from the Netherlands.

According to the record of treatment, the child was admitted to the hospital for an “undesirable post-vaccinal manifestation” and “intoxication by meningitis A vaccine.” Over the course of the hospital stay, the child suffered from headaches, shaking, vomiting, intense abdominal pain, and “contractions,” which likely refers to seizures.

Sadly, this child was prescribed Largactil, a psychiatric drug used to treat schizophrenia, probably due to the fact that members of the government have insisted that the paralyzed children’s afflictions were all in their heads. There is no mention in the clinical records of any prescription or treatment for pain relief or seizures.

This medical record, as well as the others sent to VacTruth by parents, demonstrates that these children need continued medical care. Yet, the ill children have been returned to an isolated, poorly equipped village far from sufficient available help!

It has since been reported by Ecoterra International that the conditions of at least ten children have deteriorated since being evacuated. [10]

POLIO RATES SKYROCKET IN THE MIDST OF VACCINATION CAMPAIGNS

As if the poorest regions of Africa has not had enough problems, GlaxoSmithKline has decided that they would get in on the act. Ethan A. Huff from Natural News reported on Feburary 19, 2013, that GlaxoSmithKline has teamed up with the company Biological E Ltd. and together they have decided that is a great idea to give the children of Africa a six-in-one vaccine. This is a single-dose vaccine for polio, diphtheria, tetanus, whooping cough (pertussis), hepatitis B, and Haemophilus influenzae type B.

This vaccine will be specifically designed for the poorest children of world. Natural News says:

“According to reports, GSK will add the contents of its injectable polio shot to a pentavalent vaccine already being manufactured by Biological E Ltd. that contains the other five vaccines. Together, as part of a 50-50 joint venture, the two companies will manufacture the hexavalent vaccine, which will rival similar combination vaccines for polio currently being developed and administered by rival drug companies in India such as Serum Institute of India Ltd. and Sanofi Pasteur.” [11]

According to Natural News, a study published in the Indian Journal of Medical Ethics (IJME) found that cases of polio-related paralysis have skyrocketed as a result of widespread polio vaccine campaigns throughout India, which means the populations of India are not benefiting from existing polio vaccines as the vaccine industry claims they are. So the two companies decided to put their heads together and come up with a new vaccine to boost their own economy.

In other words if at first you do not succeed, try, try, try again!

Dr. Rebecca Carley made her feelings abundantly clear about vaccines being used as bioweapons in an article recently, while the resulting damage is hidden from the public. She wrote:

“As I continue to follow the ongoing vaccine induced genocide of the indigenous Tibu children in Chad, Africa, it has become obvious that the totality of the documents I have accrued over the years has now reached critical mass for the purpose of going on the offensive against the psychopaths orchestrating the depopulation agenda. This was the topic of my RBN show on 2/10/13; you can access the archive for free by going to http://thelightofdayradioshow.com/archives/RBN-BACKUP/New-RBN-Dr-Carley-Archives.html. [12]

Dr. Carley is right, as there is no better way of covering up adverse events than dumping sick children in the middle of nowhere and leaving them to die, is there? The saying  ‘out of sight, out of mind’ springs to mind.

CONCLUSION

It appears that Mr. Gates will go to any lengths to vaccinate the world, even if the world makes it very clear that they do not want his vaccines. Rather than vaccinating more children, if he was such a humanitarian, why has he allowed vulnerable, sick children to be dumped in the middle of nowhere to die? Surely the world would applaud him far more loudly if he spent his millions making sure that any vaccine casualties were sufficiently cared for.

References

1. http://www.telegraph.co.uk/technology/bill-gates/9812672/…
2. http://www.guardian.co.uk/world/2012/dec/18/polio…
3. http://www.guardian.co.uk/world/2013/feb/08/gunmen-nigeria-kill-polio-workers
4. http://thinktwice.com/birthcon.htm
5. http://www.tolerance.ca/Article.aspx?ID=157421&L=en
6. http://vactruth.com/2013/01/06/paralyzed-after-meningitis-vaccine/
7. http://vactruth.com/2013/01/13/children-paralyzed-by-vaccine/
8. http://vactruth.com/2013/01/25/paralyzed-symptoms-in-head/
9. http://vactruth.com/2013/02/12/vaccine-cover-up/
10. http://www.groundreport.com/World/Do-to-them-what-they-are…
11. http://www.naturalnews.com039160_glaxosmithkline_vaccines_developing…
12. http://thelightofdayradioshow.com/archives/RBN-BACKUP/…

 

8 Damn Good Reasons Not to Get the Flu Shot

By JEFFRY J. AUFDERHEIDE | VACTRUTH | FEBRUARY 4, 2013

Every year the mainstream media war drum beats for you to get vaccinated against the flu. They rarely discuss anything but the benefits of the vaccine.

Why?

Maybe it is because many people are already skeptical about the flu vaccine.

I’m going to be very up front with you here. You rarely hear about the adverse reactions or about the toxic chemicals being injected into you. My goal is to get you to investigate vaccines more closely. Here are eight reasons to question the flu shot.

Let’s begin…

REASON #1: NEUROTOXIC INGREDIENTS

A common urban myth is that the mercury has been taken out of vaccines. This is not true.

Several of the flu vaccines contain a neurotoxic ingredient called thimerosal (mercury). Each one of the flu vaccines listed below contains 25 micrograms of mercury. [1] The vaccines are:

  • Afluria CSL (Limited for Merck)
  • FluLaval (GlaxoSmithKline)
  • Fluvirin (Novartis)
  • Fluzone (Sanofi Pasteur)

Keep in mind you are being told conflicting stories.

After parents and scientists discovered that mercury was present in the vaccines, they had concerns about the substance causing neurological problems in children.

Organizations such as the American Academy of Pediatrics and the Centers for Disease Control have told you mercury in the vaccines isn’t bad for us, but as a precaution, it will be taken out of the vaccines.

Now the same organizations are telling parents if mercury isn’t kept it in the vaccines, millions will suffer. Why? Removing the mercury from vaccines would cause a major disruption in the manufacturing and supply of vaccines.[2]

Much of the evidence on the toxicity of thimerosal was swept under the rug at a secret meeting held by the Centers for Disease Control in Simpsonwood, Georgia. I’d like to invite you to read a few quotes from the meeting. I think you will see why the Centers for Disease Control wants to keep the lid on thimerosal.

Here are three important quotes from the Simpsonwood Document:

…the number of dose related relationships [between mercury and autism] are linear and statistically significant. You can play with this all you want. They are linear. They are statistically significant.” – Dr. William Weil, American Academy of Pediatrics. Simpsonwood, GA, June 7, 2000

“Forgive this personal comment, but I got called out at eight o’clock for an emergency call and my daughter-in-law delivered a son by c-section. Our first male in the line of the next generation and I do not want that grandson to get a Thimerosal containing vaccine until we know better what is going on. It will probably take a long time. In the meantime, and I know there are probably implications for this internationally, but in the meanwhile I think I want that grandson to only be given Thimerosal-free vaccines.” – Dr. Robert Johnson, Immunologist, University of Colorado, Simpsonwood, GA, June 7, 2000

But there is now the point at which the research results have to be handled, and even if this committee decides that there is no association and that information gets out, the work has been done and through the freedom of information that will be taken by others and will be used in other ways beyond the control of this group. And I am very concerned about that as I suspect that it is already too late to do anything regardless of any professional body and what they say…My mandate as I sit here in this group is to make sure at the end of the day that 100,000,000 are immunized with DTP, Hepatitis B and if possible Hib, this year, next year and for many years to come, and that will have to be with thimerosal containing vaccines unless a miracle occurs and an alternative is found quickly and is tried and found to be safe.” – Dr. John Clements, World Health Organization, Simpsonwood, GA, June 7, 2000 [3]

We at VacTruth encourage you to investigate what is being injected into your child.

 REASON #2: 4250% INCREASE IN FETAL DEATHS REPORTED

Speaking of mercury being unsafe — if you’re pregnant, beware of doctors using aggressive fear tactics pushing you to get vaccinated. Here’s why…

On September 27, 2012, the Human and Environmental Toxicology Journal (HET) published a study by Dr. Gary Goldman reporting a 4,250 percent increase in the number of miscarriages and stillbirths reported to VAERS in the 2009/2010 flu season. [4]

That year the Centers for Disease Control (CDC) had recommended the double-dosing pregnant mothers with two flu shots spiked with mercury.

In his abstract, Goldman said:

“The aim of this study was to compare the number of inactivated-influenza vaccine–related spontaneous abortion and stillbirth (SB) reports in the Vaccine Adverse Event Reporting System (VAERS) database during three consecutive flu seasons beginning 2008/2009 and assess the relative fetal death reports associated with the two-vaccine 2009/2010 season.” [4]

How can injecting these filthy vaccines into pregnant mothers be remotely safe?

 REASON #3: VACCINE-INDUCED NARCOLEPSY

Do you recall the vaccine-frenzied media telling us to get our flu shots during the H1N1 pandemic? What they didn’t tell you are the possible long-term side effects of those vaccines that are now being revealed.

Recent news about the flu vaccine suspects one of the experimental vaccines causing narcolepsy in about 800 European children. [5]

Specifically, two studies in Finland directly point the finger at the vaccine. [6, 7]

The conclusion of one study states:

“We observed a 17-fold increase in the annual incidence of narcolepsy in 2010 as compared to previous years in children aged under 17 years of age. A common feature in the history of our 54 newly diagnosed childhood narcoleptic patients was that 50 children had received an adjuvanted pandemic influenza vaccine (Pandemrix) within 8 months before the onset of symptoms. In most cases, the development of symptoms was fast. We consider it likely that Pandemrix vaccination contributed to the increased incidence of narcolepsy in Finland…” [7]

The children’s misfortune is they now have to deal with an illness that all but destroys their once normal life. Do you think the pharmaceutical companies will take any responsibility?

 REASON #4: “THEY ARE PROTECTED” … FROM YOU!

I’m not sure about other countries, but in the United States, if your child is harmed by a vaccine, there is little action you can take legally.

The 1986 National Childhood Vaccine Injury Act was passed was to protect pharmaceutical companies from anyone claiming a vaccine injured their child. Under this law, no parent can sue a vaccine manufacturer. [8]

If you decide to vaccinate your children, you do so at your own risk. No vaccine manufacturer is liable for your child’s vaccine-related injury or death from a recommended vaccine, regardless if the FDA or CDC helped get an untested flu vaccine approved.

 REASON #5: IF YOU GET VACCINATED, YOU SHED THE VIRUS

If getting injected with neurotoxins or suffering from narcolepsy isn’t enough, expect to shed the flu virus and likely infect others if you decide to get the nasal spray vaccine.

Information from the Centers for Disease Control website indicates “that both children and adults vaccinated with live-attenuated influenza vaccine (LAIV) can shed vaccine viruses after vaccination, although in lower amounts than occur typically with shedding of wild-type influenza viruses.” [9]

In one study of children in a daycare setting, 80% of vaccine recipients shed one or more virus strains for an average of 7.5 days. [9]

 REASON #6: IF YOU GET THE FLU VACCINE, EXPECT TO GET THE FLU

This might be a shock to you – if you investigate the vaccine carefully enough, you’ll discover that getting vaccinated can actually predispose you to getting the flu!

One particular study surprised researchers when they discovered “a significant positive association between the seasonal influenza vaccine and lab confirmed pH1N1 was observed.” [10]

As anecdotal evidence, you may or may not have seen what happened to television host Piers Morgan. If you didn’t, here is the condensed version.

Piers Morgan went on the Dr. Oz television show to get injected with the toxic flu vaccine in front of a live audience. Days later he came down with the flu. [11]

Did the flu vaccine cause him to get the flu? You can decide for yourself on this one.

 REASON #7: EVERY YEAR THE EXPERTS GUESS

Do you know how the flu strain is picked to put into the vaccine every year? The “experts” guess.

Every year, the influenza viruses in the seasonal flu vaccine are selected through calculations about what flu viruses are most likely to cause illness in the coming season. The FDA, acting in concert with the CDC, decides what vaccine strains for influenza vaccines to be sold in the U.S. [12]

What happens if the virus mutates or the “experts” guess incorrectly? Please see Reason #1…

 REASON #8: THE CENTERS FOR DISEASE CONTROL’S RECIPE FOR GENERATING FEAR

Many people believe the Centers for Disease Control is beyond using propaganda ploys. You might get a different impression from the information I’m about to share with you. It may seem as if the CDC fears you into getting vaccinated, much like doctors do.

What do I mean and where is this recipe?

Some years ago, the associate director for communications for the national immunization program, Glen Nowak, made a presentation entitled Planning for the 2004-05 Influenza Vaccination Season: A Communication Situation Analysis.

I am going to include the entire “recipe” so you can see the complexity of the propaganda being regularly used on you to get vaccinated.

The slide on page 27 of the presentation reads:

“Recipe” that Fosters Higher Interest and Demand for Influenza Vaccine

1. Influenza’s arrival coincides with immunization “season” (i.e., when people can take action)

2. Dominant strain and/or initial cases of disease are:

–Associated with severe illness and/or outcomes

–Occur among people for whom influenza is not generally perceived to cause serious complications (e.g., children, healthy adults, healthy seniors)

–In cities and communities with significant media outlets (e.g., daily newspapers, major TV stations)

3. Medical experts and public health authorities publicly (e.g., via media) state concern and alarm (and predict dire outcomes)–and urge influenza vaccination.

4. The combination of ‘2’ and ‘3’ result in:

A. Significant media interest and attention

B. Framing of the flu season in terms that motivate behavior (e.g., as “very severe,” “more severe than last or past years,” “deadly”)

C. Continued reports (e.g., from health officials and media) that influenza is causing severe illness and/or affecting lots of people–helping foster the perception that many people are susceptible to a bad case of influenza.

6. Visible/tangible examples of the seriousness of the illness (e.g., pictures of children, families of those affected coming forward) and people getting vaccinated (the first to motivate, the latter to reinforce)

7. References to, and discussions, of pandemic influenza– along with continued reference to the importance of vaccination.” [13]

The message is extremely familiar. You see it played out every year on the news channels. To be clear, what you just read is a recipe to sell more of Big Pharma’s toxic vaccines.

References

1. http://www.vaccinesafety.edu/thi-table.htm

2. http://vactruth.com/2012/12/23/mercury-in-vaccines/

3. http://www.putchildrenfirst.org/chapter2.html

4. http://het.sagepub.com/content/early/2012/09/12/0960327112455067.abstract?rss=1

5. http://www.reuters.com/article/2013/01/22/us-narcolepsy…

6. http://www.plosone.org/article/info:doi/10.1371/journal.pone.0033536#close

7. http://www.plosone.org/article/info%3Adoi/10.1371/journal.pone.0033723

8. http://www.hrsa.gov/vaccinecompensation/index.html

9. http://www.cdc.gov/flu/professionals/acip/laiv-shed.htm

10. http://www.ncbi.nlm.nih.gov/pubmed/22001885

11. http://www.infowars.com/piers-morgan-falls-ill-days-after-receiving-flu-vaccine/

12. http://www.cdc.gov/flu/professionals/vaccination/virusqa.htm

13. http://www.scribd.com/doc/19212191/2004flunowak

1,742 new reasons to avoid Infanrix Hexa vaccine cocktail

By CHRISTINA ENGLAND | VACTRUTH | DECEMBER 28, 2012

Last week, VacTruth reported details of the 1,271 page confidential GlaxoSmithKline document, regarding their six-in-one vaccine. More confidential papers have recently been leaked to the press. The Belgian website Initiative Citoyeene  reported both leaked documents.

The latest confidential document concerns the Prevenar 13 vaccine, a pneumococcal vaccine manufactured by Pfizer (now merged with Wyeth). [1] This vaccine replaced the original 2010 vaccine Prevenar, which, as reported by the manufacturer, has actually increased, rather than decreased, serious infections.

The Prevenar 13 protects infants against Streptococcus pneumoniae bacteria which can lead to cases of meningitis, bacteraemia (an infection of the blood), pneumonia and ear infections. [2] It is usual for the six-in-one vaccination Infanrix Hexa and the Prevenar 13 vaccine to be administered to small babies at the same time.

According to the leaked confidential Wyeth (Pfizer) documents and a reply from the European Medicines Agency (EMA), both the manufacturer and the agency are aware of a significantly higher number of adverse neurological events in children vaccinated with both Prevenar 13 AND Infanrix Hexa, as per the Belgian vaccination schedule at ages two months and four months.

 THE FIRST SET OF LEAKED DOCUMENTS

First, let’s revisit the leaked confidential document regarding the Infanrix Hexa vaccine information, which I revealed just days ago on VacTruth. I exposed a hidden GlaxoSmithKline document that had been leaked to the press, revealing 36 infant deaths. [3]

The document, titled Confidential To Regulatory Authorities Infanrix Hexa Summary Bridging Report [4] stated that between October 23, 2009, and October 22, 2011, GlaxoSmithKline received a total of 1,742 reports of adverse events, including 503 serious adverse events, after children had received the 6 in 1 vaccine, Infanrix Hexa.

(Infanrix Hexa is a 6-in-1 vaccination, which combines the Combined Diphtheria, Tetanus and Acellular Pertussis, Hepatitis B enhanced Inactivated Poliomyelitis and the Haemophilus influenzae type B vaccine. It is used in 92 countries worldwide.)

The GlaxoSmithKline confidential document detailed each and every one of the 1,742 adverse events. The list was so long, it required a full twenty pages. Here are some of the adverse events detailed on charts between pages 11 and 31 of their document:

  • 106 cases of cyanosis

  • 69 cases of loss of consciousness

  • 165 cases of hypotonia

  • 102 cases of hypotonic-hyporesponsive episodes

  • 107 cases of convulsions

  • 20 cases of epilepsy

  • 98 cases of febrile convulsions

  • 33 cases of grand mal convulsions

  • 47 apnea attacks

  • 108 cases of vomiting

  • 43 cases of Gaze Palsy

  • 12 cases of anemia

  • 1 case of bone marrow failure

  • 6 cases of cardiac arrests

  • 53 cases of diarrhea

  • 593 cases of pyrexia (high temperature)

  • 22 cases of gait disturbance

  • 6 cases of anaphylaxis

  • 62 cases of pertussis (whooping cough)

  • 2 cases of meningitis pneumococcal

  • 3 cases of arthritis

  • 16 cases of muscle twitching

  • 22 cases of tremors

  • 264 cases of crying (does not indicate the severity)

  • 2 cases of Guillain-Barre syndrome

  • 10 cases of respiratory arrest

  • 7 cases of Kawasaki’s disease

All of these adverse events occurred after the child received the Infanrix Hexa vaccination, some just hours after being vaccinated. I am sure you will agree that these documented facts make extremely uncomfortable reading.

However, if this information is not disturbing enough, in the document, GlaxoSmithKline revealed on page twenty a total of 68 cases of vaccination failure! This fact proves that, not only does their vaccine appear to cause death, injury and illness in multiple children, but that this vaccine failed to give any “protection” at all to at least 68 children.

The document was signed by Safety Scientist Vanessa Corman and Vice President, Lead Biological Clinical Safety and Pharmacovigilance Dr. Felix Arellano, M.D., from GlaxoSmithKline Biologicals.

THE SECOND SET OF LEAKED DOCUMENTS

Now, let’s continue with the shocking new papers that the Belgian website Initiative Citoyeene have revealed. They stated:

“On the 4th of January this year, at the end of the required 6-week period, two Pfizer Group Regulatory Affairs Directors, Mary Allin and Helen Edwards, sent a response to Dr. S. Spinosa of the European Medicine Agency on the topic of ‘higher number of neurologic events reported in Italy following the coadministration of Pevenar 13 and hexavalent vaccines.’ The two directors specified at the end of this letter that based on data supplied, they did not feel there was any need to modify the vaccine’s reference safety information (RSI), in other words, its package insert.”

So, let’s take a closer look at one of the confidential reports that Initiative Citoyenne has been quoting. This confidential document reveals that over a two-year period, 22 deaths were reported, representing 2.6% of the total number of cases and a total of 51 reported cases of lack of efficacy, or vaccination failure! [4]

BRAIN DAMAGE AND DEATH

The next section relates to reports of neurological events.

The Master of Health Administration (MAH), was asked by the Committee for Medicinal Products for Human Use (CHMP), to provide a cumulative review of neurological reactions in those cases, which were reported to have received Prevenar 13 concomitantly (at the same time) with hexavalent (6-in-1) vaccine.

The MAH reported that during the two-year period between July 10, 2009, and July 9, 2011, a total of 1,691 cases of adverse events were reported after the Prevenar 13 vaccine. Of those adverse events, 312 cases (18%) were indicative of neurological reactions. [5] The 1,691 cases were then divided in three different datasets. The Initiative Citoyenne website explained the findings:

“An important fact is that Pfizer assessed the respective frequency of neurologic accidents in three different groups of children: those who had all received only the Prevenar 13 on the same day, those who had received both the Prevenar 13and other vaccines on the same day and those who had received both the Prevenar 13 and a hexavalent vaccine on the same day.

Of the 934 children who had only received the Prevenar 13 and experienced adverse effects, 87 displayed neurologic events (87/934 = 9%).

Of the 287 children who had received the Prevenar 13 plus other vaccines on the same day, and experienced adverse effects, 62 had had neurologic episodes (62/287 = 21%).

Of the 470 children who received the Prevenar 13 plus a hexavalent vaccine, on the same day, and reported adverse effects, 163 had experienced neurologic reactions (163/470 = 34%!!). It is therefore clear that the concomitant administration of several vaccines, particularly those recommended in the Belgian vaccine schedule (Prevenar 13 alongside Infanrix Hexa), multiplies the risk of neurologic reactions including serious and potentially irreversible adverse events!”

To describe the enormity of the situation, they further stated, in easy-to-understand terms:

“To grasp the extent of the problem, just remember that the Belgian annual birth rate is approximately 128,000, a very large majority of whom receive BOTH the Prevenar and the Infanrix Hexa. A simple calculation reveals therefore that the annual number of serious adverse effects, taking ONLY this vaccine into account, could be 3% x 128,000 births = 3,840 children!”

MORE REASONS TO AVOID THIS SIX-IN-ONE VACCINE

Interestingly, the Prevenar 13 leaflet mentioned earlier states reasons why your child should not be given Prevenar 13:

“Your child should not have Prevenar 13 if he or she has ever had an allergic reaction to pneumococcal or DIPTHERIA VACCINES, or any of the ingredients listed at the end of this leaflet.”

Despite this warning, the Prevenar 13 vaccine is often given at the same time the Infanrix Hexa vaccine, which includes a diptheria component! These vaccines are recommended from as early as six weeks of age, according to the leaflet, at which time a parent would not know whether their child was allergic to the diptheria component or not.

One Belgian child who lost her life as a consequence of being given several vaccinations in one visit, which included the Infanrix Hexa vaccine together with Prevenar, was Stacy Sirjacobs. Stacy was an eight week-old premature twin who died in December 2011. [6]

These vaccines were given to Stacy despite advice given by the European Medicines Agency in their ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS for Infanrix Hexa report which stated:

“When Infanrix Hexa is co-administered with Prevenar (pneumococcal saccharide conjugated vaccine, adsorbed), the physician should be aware that data from clinical studies indicate that the rate of febrile reactions was higher compared to that occurring following the administration of Infanrix Hexa alone.”
[7]

Furthermore, the document contained information about administering the vaccine to premature infants:

Limited data in 169 premature infants indicate that Infanrix Hexa can be given to premature children. However, a lower immune response may be observed and the level of clinical protection remains unknown.

The potential risk of apnea and the need for respiratory monitoring for 48-72h should be considered when administering the primary immunisation series to very premature infants (born ≤ 28 weeks of gestation) and particularly for those with a previous history of respiratory immaturity.”

TROUBLING QUESTIONS

The European Medicines Agency offered warnings about administering the vaccine concomitantly with another vaccine and cautioned health care providers to consider the additional risks of vaccinating premature infants. Then why was little Stacy, a baby born one month prematurely, delivered by Caesarean section, resuscitated at birth, who spent the next four days in an incubator, given these vaccinations and then sent home without any extra advice?

Her death was a tragedy, yet babies are still dying and being neurologically damaged on a regular basis. The proof is in the manufacturer’s report in black and white. The drug companies know, the regulatory agencies know and worse still, our governments know.

Slowly, day-by-day, the depth of their corruption is being uncovered. Parents are not being told the truth, they are being deceived and lied to and the price they pay is extremely high.

CONCLUSION

These adverse events were being reported as far back as 2009.  So, why are these two vaccines still being recommended for babies as young as 6 weeks old? Surely, the most sensible and responsible action would be for the manufacturers GlaxoSmithKline and Pfizer to suspend the use of these vaccines until their use can be shown to be reliable, effective, and safe. Instead, this information is being hidden from the public.

Furthermore, the mainstream media is so quiet you could hear a pin drop. Dr. Rebecca Carley, an expert specializing vaccine-induced diseases syndromes, has often stated on her radio shows that vaccinations are the ‘True Weapons of Mass Destruction,” and the evidence contained in these leaked, confidential documents shows she could be right.

Acknowledgements

The author would like to thank the website Initiative Citoyenne for bravely revealing the truth.

The staff at VacTruth wishes to express their heartfelt condolences to the family of Stacy Sirjacobs and other families whose children have suffered injuries or death following vaccination.

References

  1. Initiative Citoyenne Press Release http://ddata.over-blog.com/3/27/09/71/2012-2013…
  2. Prevenar 13 leaflet Consumer Medical Information http://www.nps.org.au/__data/assets…
  3. http://vactruth.com/2012/12/16/36-infants-dead-after-vaccine/
  4. Confidential To Regulatory Authorities Infanrix TM hexa Summary Bridging Report http://ddata.over-blog.com/3/27/09/71/2012-2013/confid.pdf
  5. Prevenar 13 PSUR 04 – Response to RSI Neurological Events PFIZER CONFIDENTIAL Page 1 Prevenar 13 Pneumococcal saccharide conjugated vaccine, 13 valent adsorbed PSUR 04 – Response to Question on Neurological events http://ddata.over-blog.com/xxxyyy/3/27/09/71/2012-2013/emea-responses–Prevenar-13-Pfizer-Confidential.pdf
  6. http://vactruth.com/2012/01/19/baby-dies-after-first-shots/
  7. European Medicines Agency ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS for Infranrix Hexa http://www.ema.europa.eu/docs/en_GB/document_library

36 infants dead after receiving GlaxoSmithKline’s 6 in 1 Vaccine

By CHRISTINA ENGLAND | VACTRUTH | DECEMBER 17, 2012

A confidential GlaxoSmithKline document recently leaked to the press exposed that within a two-year period, a total of 36 infants died after receiving the 6-in-1 vaccine, Infanrix Hexa. [1] According to the website Initiative Citoyenne [2] who reported the news, the 1271 page document revealed that GlaxoSmithKline received a total of 1,742 reports of adverse reactions between October 23, 2009, and October 22, 2011, including 503 serious adverse reactions and 36 deaths. Initiative Citoyenne stated:

“It’s not that 14 deaths were recorded by GSK between October 2009 and end in October 2011 as we had originally calculated but 36 (14 from 2010 to 2011 and 22 from 2009 to 2010). In addition to these 36 deaths at least 37 other deaths (sudden death mainly), bringing the total to at least 73 deaths since the launch of the vaccine in 2000, and again, this concerns only the death by sudden death, no further recovery of under-reporting.”

Using the figure of 36 deaths over a two-year period, this averages 1.5 deaths per month, which by anyone’s standard is extremely high. Note that only 1 to 10% of adverse reactions to vaccines are actually reported. Therefore, in reality, the problem could potentially be far more serious and the actual number of fatalities much higher.

THE DEADLY CHEMICAL COCKTAIL

The charts show that many of the babies who died passed away within the first few days of receiving the vaccine. [3] A total of three infants were reported to have died within hours of receiving the vaccine. This tragedy is hardly surprising given the vaccine’s ingredients listed on the GSK Infanrix Hexa product information leaflet, which parents are rarely given the chance to read prior to vaccination, including non-infectious substances from tetanus, diphtheria bacteria, purified proteins of pertussis bacteria, the surface protein of the hepatitis B virus (HBsAg, derived from genetically engineered yeast cells) and inactivated poliovirus. [4] Each 0.5mL dose contains:
  • diphtheria toxoid
  • tetanus toxoid
  • pertussis toxoid
  • filamentous haemagglutinin
  • pertactin
  • recombinant HBsAg protein
  • poliovirus Type 1
  • poliovirus Type 2
  • poliovirus Type 3
  • purified capsular polysaccharide of Hib covalently bound to tetanus toxoid
  • aluminium hydroxide
  • aluminium phosphate
  • 2-phenoxyethanol, lactose
  • Medium 199
  • neomycin
  • polymyxin
  • polysorbate 80
  • polysorbate 20
  • sodium chloride
  • water

TOXIC DOSES OF TOXIC CHEMICALS

In an interesting article by Dr. Harold Buttram titled “The Ultimate Gamble: Do Childhood Vaccines Result in Genetic Hybridization from Alien Human and Animal DNA Contents?” he highlighted the problems associated with just two of these ingredients, including aluminum, which is a neurotoxin associated with Alzheimer’s disease and seizures, and formaldehyde, which is a known cancer-causing agent commonly used to embalm corpses. [5]

Dr. Harold Buttram also stated:

“It is universally recognized among toxicologists that combinations of toxic chemicals may bring exponential increases in toxicity; that is, two toxic chemicals in combination will bring a ten-fold or even a hundred-fold increase in toxicity. 

A classical example of this principle was the Schubert study [21] in which it was found that the amount of lead and the amount of mercury, when each was given separately, would be lethal for one percent of rats tested, would become lethal for one hundred percent of rats tested when combined.

In vaccines this principle would apply at least to mercury and aluminum, both of which are potent neurotoxins.”

CONCLUSION

Considering this information, is it any wonder that babies are dying after receiving vaccinations containing these ingredients? GlaxoSmithKline may try and hide the facts from us but they cannot hide them forever. Infanrix Hexa should be removed from the market immediately.

References

  1. Confidential To Regulatory Authorities – Biological Clinical Safety and Pharmacovgilance – GlaxoSmithKline Research and Development Avenue Fleming 20 1300 Wavre Belgium http://ddata.over-blog.com/xxxyyy/3/27/09/71/2012-2013/confid.pdf
  2. Initiative Citoyenne http://ddata.over-blog.com/xxxyyy/3/27/09/71/2012-2013/Communique-de-presse-d-IC-du-6-dec.-2012-_doc-confidentie.pdf
  3. Initiative Citoyenne Charts http://www.initiativecitoyenne.be/article-infanrix-hexa-le-document-confidentiel-accablant-113251207.html
  4. Infanrix Hexa product information leaflet http://www.betterhealth.vic.gov.au/bhcv2/bhcmed.nsf/pages/gwcinfih/$File/gwcinfih.pdf
  5. Dr Harold Buttram The Ultimate Gamble: Do Childhood Vaccines Result in Genetic Hybridization from Alien Human and Animal DNA Contents?” http://vactruth.com/2012/03/13/vaccines-human-animal-dna/