Piers Morgan Falls Ill Days After Public Flu Shot with Dr. Oz

Natural Society
by Anthony Gucciardi

Just two days after it was reported that GlaxoSmithKline’s Pandemrix H1N1 swine flu vaccine has actually caused a whopping 800 cases of narcolepsy in children according to Reuters, a major publicity stunt for the efficacy of the flu shot as presented by CNN has crashed and burned. After receiving his very first flu shot live on air from vaccine advocate Dr. Oz in attempt to showcase the ‘safety and effectiveness of the shot’, Piers Morgan has now developed flu-like symptoms that even he and his guest have attributed to the reception of the shot.

In the January 23 interview with country music celebrity Dwight Yoakam, Piers and Dwight discuss the connection between the recent shot and his new sickness. In the interview, which can be seen below, Piers asks “…As you can tell, things are deteriorating. Is there any advice you can give me?”

Yoakam replies with a simple “Don’t ever take a flu shot again,” sparking further discussion surrounding the public injection that ultimately turned into a PR nightmare for Big Pharma. In a surprising reply, Piers says ““We’re both doing the math, so I mean, we both saw him put that thing in my arm and within 10 days I’m struck down.” It was Piers’ first flu shot in his life, according to his own testimony.

You can watch this segment below:

As pointed out by Adan Salazar, the sickness is also highly ironic as Piers actually questioned Dr. Oz about the so-called ‘myths’ surrounding the shot before it was administered. One such ‘myth’ was whether or not the shot could actually lead to the flu. In dialogue with Dr. Oz, Piers nervously asked:

“So the myth about these, and I’m told it’s a myth, is that you can actually get flu or flu-like symptoms simply by having the shot. Is that true?”

Dr. Oz, of course, regurgitated information provided by the CDC in stating that such an event is impossible due to the fact that the flu shot contains the dead flu virus. Dr. Oz also fails to mention that even the FDA’s own website admits that vaccines contain toxic additives like:

Antibiotics: Linked to the development of mental illness, obesity, and serious gut imbalance due to the depletion of beneficial bacteria in the gut, superbug-spawning antibiotics are used in vaccinations as an ‘additive’ as admitted by the FDA.

Formaldehyde: This of course is the known carcinogen used in the preservation of corpses by funeral homes and elsewhere. Even Cancer.gov admits that formaldehyde is a serious cancer-causing chemical, stating “Formaldehyde has been classified as a known human carcinogen (cancer-causing substance) by the International Agency for Research on Cancer…” So why is this cancer-causing substance being used an additive for vaccinations?

Aluminum: Popularly associated with Alzheimer’s disease and a bunch of other brain disorders, aluminum is used as a vaccine additive to ‘stimulate a response’ from the body.

Thimerosal: One of the most widely known additives, thimerosal is a mercury-containing substance that is unsafe at any dose. Your doctor is likely entirely misinformed on this additive, stating there is no mercury-containing thimerosal in a vaccine when even the FDA and CDC plainly state this. As stated by Dr. David Wallinga from the Institute for Agriculture and Trade Policy, mercury is ‘toxic in all its forms.”

Instead of giving Piers a vaccination full of these toxic additives, Dr. Oz could have simply recommended that Piers begin supplementing with high quality, inexpensive vitamin D3 — or simply take a walk around outside in a warmer climate. Even in considerably low doses, vitamin D3 has been found to flash the risk of flu development by nearly half – a much great success rate than the flu shot.

Get Your Flu Shot or Get Fired: Media Hails New ‘Safety’ Policies Forcing Shots on Workers

Natural Society
by Anthony Gucciardi

Don’t want to be injected with the seasonal flu vaccine due to concerns over ingredients like MSG, antibiotics, formaldehyde, and aluminum as admitted by the FDA on their own website? Well then you may lose your job for refusing a ‘safety’ measure, as more and more major corporations are forcing the flu vaccine (among others) on workers in order to keep their job.

But how is this being enabled? Despite being met with massive resistance as vaccination rates are actually declining across the board due to concerns by citizens worldwide, mainstream media organizations like the Chicago Chronicle have been running numerous hit pieces on those who reject the flu vaccine as ‘uninformed’ and just plain old silly.

These articles also champion in the ‘safety’ measures of forced vaccination within mega corporations like Alexian Brothers Health System with unquestioning loyalty towards the companies. Dismissing any legitimate civil or health concerns with a laughable ‘oh, stop’ and no actual response, this mainstream media article was actually published to the tens of millions that read the Chicago Chronicle each month.

Media: ‘Stop’ Questioning Corporations!

When addressing the real concerns regarding how a corporation can force an employee to inject themselves with MSG, antibiotics, aluminum, and other contaminants, the Chicago Chronicle just dismisses it without question. The article reads:

“If your employer can order you to inject or inhale a vaccine, the reasoning goes, what else might it require? Oh, stop. A hospital isn’t out of line when it tells its employees to get vaccinated — or get fired.”

Just as the Chronicle states, the corporate media desperately wants you to please stop asking virtually any questions. After all, it makes whitewashing the news and propagating literal fabrications very challenging. Even the European Union Food Safety Agency asked scientists and consumers to please stop studying genetically modified organisms following the breaking report that GMOs had been linked to tumors.

Of course media pieces like these are actually a bi-product of resistance from the people. As more and more individuals refuse the carcinogen-packed flu shot on a yearly basis, vaccine manufacturers are in a panic. Big Pharma as a whole is in trouble, and the only way they know how to perform damage control is through spending millions upon millions in PR runs.

All of the PR runs and media campaigns to dismiss legitimate concerns (without ever actually addressing them beyond a sarcastic or satirical discount like ‘oh, stop’) cannot, however, stop the emergence of real information to the public regarding GMOs, the contaminants within the flu shot, and other items.

The mainstream media and mega corporations would like you to please stop questioning their actions, but they will never get their wish.

Vaccine Bombshell: Leaked Confidential Document Exposes 36 Infants Dead After This Vaccine

VacTruth
By Christina England

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- vaccine, Infanrix Hexa. According to the website Initiative Citoyenne 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. 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. 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.

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 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.

Vaccine Bombshell: Baby Monkeys Develop Autism Symptoms After Obtaining Doses of Popular Vaccines

by Sola Ogundipe

Following a recent study conducted by scientists at the University of Pittsburgh, Pennsylvania which revealed that many infant monkeys given standard doses of childhood vaccines as part of the new research,developed autism symptoms, question marks over the ultimate safety of vaccines have come to the fore.

The groundbreaking research findings presented at the International Meeting for Autism Research (IMFAR) in London, England, have revealed that young macaque monkeys given the typical CDC-recommended vaccination schedule from the 1990s, and in appropriate doses for the monkeys’ sizes and ages, tended to develop autism symptoms. Theirunvaccinated counterparts, on the other hand, developed no such symptoms, which points to a strong connection between vaccines and autism spectrum disorders.

This development which deconstructs mainstream myth that vaccines are safe and pose no risk of autism, was brought on by after studies on the type of proper safety research on typical childhood vaccination schedules that the U.S. Centers for Disease Control and Prevention (CDC) should have conducted — but never has — for such regimens.

Included in the mix were vaccines containing Thimerosal, a toxic, mercury-based compound that has been phased out of some vaccines, but is still present in batch-size influenza vaccines and a few others.

Also administered was the controversial measles, mumps, and rubella (MMR) vaccine, which has been linked time and time again to causing autism and various other serious, and often irreversible, health problems in children.

“This research underscores the critical need for more investigation into immunizations, mercury, and the alterations seen in autistic children,” said Lyn Redwood, Director of SafeMinds, a public safety group working to expose the truth about vaccines and autism.

“SafeMinds calls for large scale, unbiased studies that look at autism medical conditions and the effects of vaccines given as a regimen.”

Adding to the sentiment, Theresa Wrangham, president of SafeMinds called out the CDC for failing to require proper safety studies of its recommended vaccination schedules. Unlike all other drugs, which must at least undergo a basic round of safety testing prior to approval and recommendation, vaccinations and vaccine schedules in particular do not have to be proven safe or effective before hitting the market.

“The full implications of this primate study await publication of the research in a scientific journal,” said Wrangham. “But we can say that it demonstrates how the CDC evaded their responsibility to investigate vaccine safety questions. Vaccine safety oversight should be removed from the CDC and given to an independent agency.”

Genetically Engineered Gardasil Vaccine May Contain A New Chemical With Untested Toxicity

Activist Post

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

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

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

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

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

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

Dr. Lee stated:


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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

One more critical point:

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

Dr. Lee offered the following explanation:

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

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


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

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

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

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

Related:  Gardasil. The vaccine that almost killed me, and maybe you.

DARPA’s Blue Angel – Pentagon prepares millions of vaccines against future global flu

RT

The Pentagon’s DARPA lab has announced a milestone, but it doesn’t involve drones or death missiles. Scientists at the Defense Advanced Research Projects Agency say they’ve produced 10 million doses of an influenza vaccine in only one month’s time.

In a press release out of the agency’s office this week, scientists with DARPA say they’ve reach an important step in being able to combat a flu pandemic that might someday decimate the Earth’s population. By working with the Medicago Inc. vaccine company, the Pentagon’s cutting edge research lab says that they’ve used a massive harvest of tobacco plants to help produce a plethora of flu-fighting vaccines.

“Testing confirmed that a single dose of the H1N1 VLP influenza vaccine candidate induced protective levels of hemagglutinin antibodies in an animal model when combined with a standard aluminum adjuvant,” the agency writes, while still noting, though, that “The equivalent dose required to protect humans from natural disease can only be determined by future, prospective clinical trials.”

Researchers have before relied on using chicken eggs to harvest compounds to use in influenza vaccines. With a future outbreak requiring scientists to step up with a solution as soon as possible, though, they’ve turned to tobacco plants to help produce the vaccines.

“Vaccinating susceptible populations during the initial stage of a pandemic is critical to containment,” Dr. Alan Magill, DARPA program manager, says in an official statement. “We’re looking at plant-based solutions to vaccine production as a more rapid and efficient alternative to the standard egg-based technologies, and the research is very promising.”

The World Health Organization has gone on the record to say that as much as half of the people on the planet could be affected by a pandemic in the near future, and it could take as much as nine months for a vaccine for a pandemic virus strain to become made available. With the lives of billions of people across the world at stake, DARPA has been trying to determine new ways of churning out antidotes in as little time as possible. Now its researchers say, that in only a month, scientists “produced more than 10 million doses (as defined in an animal model) of an H1N1 influenza vaccine candidate based on virus-like particles (VLP).”

Through DARPA’s previously established Blue Angel program, researchers have spent several years searching for new ways to produce mass quantities of vaccine-grade protein that could be used to combat what they say are very real emerging and novel biological threats.

Andy Sheldon, Chief Executive Officer of Medicago , says in the company’s own press release that “The completion of the rapid fire test marks a substantial achievement in demonstrating our technology and the potential for Medicago to be the first responder in the event of a pandemic flu outbreak.”

Medicago’s research was conducted in a 97,000-square-foot vaccine facility in North Carolina that was funded through a $21 million Technology Investment Agreement with DARPA.

Related: 30 Years Of Secret, Official Transcripts Reveal Government Vaccine Lies