Centers for Disease Control warns about threat posed by new, unknown virus

By JULIE STEENHUYSEN | REUTERS | MARCH 8, 2013

The Centers for Disease Control and Prevention (CDC) on Thursday warned state and local health officials about potential infections from a deadly virus previously unseen in humans that has now sickened 14 people and killed 8.

Most of the infections have occurred in the Middle East, but a new analysis of three confirmed infections in Britain suggests the virus can pass from person to person rather than from animal to humans, the CDC said in its Weekly Morbidity and Mortality Report on Thursday.

The virus is a coronavirus, part of the same family of viruses as the common cold and the deadly outbreak of Severe Acute Respiratory Syndrome (SARS) that first emerged in Asia in 2003. The new virus is not the same as SARS, but like the SARS virus, it is similar to those found in bats.

So far, no cases have been reported in the United States.

According to the CDC’s analysis, the infections in Britain started with a 60-year-old man who had recently traveled to Pakistan and Saudi Arabia and developed a respiratory illness on January 24, 2013. Samples from the man showed he was infected with both the new virus and with H1N1, or swine flu.

This man subsequently passed the infection to two members of his household: a male with an underlying illness who became ill on February 6 and subsequently died; and a healthy adult female in his household who developed a respiratory illness on February 5, but who did not need to be hospitalized and has recovered.

The CDC said people who develop a severe acute lower respiratory illness within 10 days of returning from the Arabian Peninsula or neighboring countries should continue to be evaluated according to current guidelines.

The health agency said doctors should be watchful of patients who develop an unexplained respiratory infection within 10 days of traveling from the Arabian Peninsula or neighboring countries. The CDC has set up a special website with updates on the infections at http://www.cdc.gov/coronavirus/ncv/ .

Symptoms of infection with this new virus include severe acute respiratory illness with fever, cough and shortness of breath. Neither the CDC nor the World Health Organization has issued travel restrictions related to the virus.

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Vaccine injuries in Africa being covered-up

By CHRISTINA ENGLAND | VACTRUTH | FEBRUARY 14, 2013

Millions of children across Africa have been included in meningitis vaccine trials, many without parental consent. VacTruth recently revealed this information, resulting in many agencies desperately trying to cover up this travesty and the sacking of two leading heads of state.

Shortly after VacTruth published the first of three articles covering the MenAfriVac vaccine tragedy in which dozens of children were paralyzed, in Gouro, Chad, in northern Africa, the prime minister of Chad, Emmanuel Nadingar, was relieved of his duties and replaced by the former chief of cabinet, Djimrangar Dadnadji. According to an excellent article by the human rights organization Ecoterra International, this abrupt change in leadership was ordered by Chad’s president Idris Déby, a patron of the anti-meningitis campaign. [1]

BIG NAMES, BIG MISTAKE

On January 13, 2013, VacTruth published the second of the three articles. By this time, Chadian authorities had reported that a total of 38 children who were suffering from adverse reactions to the vaccine had been evacuated to hospitals in N’Djamena, Chad’s capital. [2]

A few weeks later, VacTruth was informed that the health minister of Chad, Mamouth Nahor N’Gawara, had also been relieved of his duties and replaced by Dr. Mahamat Ahmat Djidda. [3]

So, why the sudden changes in leadership? It may have had something to do with the fact that VacTruth had reported the conflicting views from involved organizations on whether or not the MenAfriVac vaccine could be used outside of the usual controlled temperature chain (CTC) of 2 – 8 °C.

The organizations involved with the promotion of the vaccine had stated that MenAfriVac was a vaccine specifically designed to meet the needs of Africa’s meningitis belt, which stretches across sub-Saharan Africa. These organizations stated that the vaccine could be kept in a controlled temperature chain (CTC) at temperatures of up to 40°C for up to four days without the need for ice packs or refrigeration.

The organizations involved in the promotion of this information were the CDC, FDA, BMGF, PATH, MVP, WHO and UNICEF. (For meanings of these acronyms, please refer to key at the end of this article.)

YOU WON’T BELIEVE WHAT HAPPENED NEXT

Of course this information would have been fantastic news for Africa, except for one vital point: at the time we published our articles, Serum Institute of India, the manufacturer of the vaccine, was promoting conflicting information. They had stated on their website:

“MenAfriVac should be stored and transported between 2-8ºC. Protect from light. The diluent should be stored at 25°C. It is recommended to protect the reconstituted vaccine from direct sunlight. Do not exceed the expiry date stated on the external packaging.”

Here is a snapshot of the original page.

An archived snapshot of the vaccine manufacturer’s website show they changed information about the storage of the vaccine shortly after the children became paralyzed.

However, when this information was checked for verification last week, the recommendations for vaccine storage had mysteriously changed to the following statements:

“MenAfriVac should be stored and transported between 2-8ºC. Protect from light. The diluent should be stored at 25°C. It is recommended to protect the reconstituted vaccine from direct sunlight. Do not exceed the expiry date stated on the external packaging. Immediately prior to reconstitution the vaccine is stable and can be used when exposed up to 40ºC for period of 4 days provided the vaccine has not reached its expiry date and the vaccine vial monitor has not reached the discard point.” [4]

Why was this information suddenly changed, after the vaccine had already been stored and administered according to the previous guidelines? Was it because we reported that dozens of children were paralyzed and suffering other adverse reactions after receiving MenAfriVac? Was it because we reported that this vaccine was administered to third-world children before it was licensed?

In October 2012, WHO had stated:

“The session began with an introduction by Mr. Michel Zaffran, who highlighted the groundbreaking progress made with MenAfriVac®, which will be the first EPI vaccine licensed for use in a controlled temperature chain (CTC).

… This is the final review of the document by IPAC prior to the planned field testing during the MenAfriVac® campaign in Benin in November 2012, where one district will use the vaccine in a CTC. After the field testing has been conducted, the revised final guidance document will come back to IPAC for endorsement in 2013.” [5]

The reasons why the manufacturer suddenly changed their recommendations for storage and transport remain a mystery. However, this new controversy still does not take away the fact that MenAfriVac was not licensed to travel in a CTC of temperatures of up to 40°C at the time the children of Gouro were vaccinated.

THIS DOESN’T MAKE SENSE!

What exactly is a controlled temperature chain? If these vaccines do not need refrigeration or ice packs for up to four days, how does the word “controlled” come into the process? Surely, without ice packs or refrigeration, there is no controlled temperature chain.

MenAfriVac is an inactivated vaccine (a vaccine which does not use a live virus). Previously, according to the CDC guidelines for vaccine temperature and storage, inactivated vaccines needed refrigerator storage at temperatures between 35°F and 46°F (2°C to 8°C), with a desired average temperature of 40°F (5°C). (Note, that is 40°F not 40°C.) [6]

So, what makes the MenAfriVac vaccine so different from other vaccines, that it does not require refrigeration for up to four days?

Another important point to consider is the fact that temperatures across Africa can exceed 40°C. According to the website Weather Spark, the average weather for N’Djamena, Chad varies between 15°C and 41°C. Their temperatures are rarely below 12°C or above 44°C. This means that outdoor temperatures can reach 44°C in a typical year. [7] In fact, in June 2010, temperatures in Chad reached an all-time high of 47.6°C. [8]

MORE UNANSWERED QUESTIONS

This information leads me to ask the following questions:

If the outdoor temperatures can reach 44°C in a typical year and the MenAfriVac vaccine is traveling inside a vehicle which may not have air-conditioning, in a container without ice packs or refrigeration, then how do the vaccinators know the true temperature the vaccine has reached at any given time?

If the truck carrying the vaccines is traveling across Africa at the time that the outdoor temperatures rise above 40°C, does the team return to base and scrap that particular batch of vaccines?

Can both the vaccine and the diluents be kept at the same temperature?

I ask the third question because it is usual for the vaccine and the diluents to be kept at different temperatures in accordance with recommendations from the manufacturer and the CDC.

ANOTHER SUSPICIOUS TRIAL

Another interesting point to consider is this: at the time the MenAfriVac vaccine was being administered to the children in Gouro, it was being tested to see whether or not it was safe to be administered to children in temperatures of up to 40°C. Therefore, it is odd that the vaccinators chose to vaccinate the children at the time of year when temperatures are usually below 30°C.

The children of Gouro were not the only children being used in clinical trials for the MenAfriVac vaccine. Babies between the ages of 14 –18 weeks were also being used for clinical trials in Ghana.

According to the Meningitis Vaccine Project (MVP), a MenAfriVac phase 2 clinical trial was carried out in Ghana, testing the vaccine for use in the under-one age group. The trial was carried out over a four-year period from November 2008 to November 2012 at the Navrongo Health Research Center, Navrongo, Ghana. A total of 1,200 infants took part in the trial, aged between 14 to 18 weeks on enrollment. MVP stated:

“Study results: Preliminary results show that the vaccine is safe and highly immunogenic. Final results will be presented in a forthcoming scientific publication.” [9]

The MVP News Digest reported the following:

“Research to document an indication for MenAfriVac™ use in infancy (in under 1-year-olds) is progressing well and according to schedule. A database lock for PsA-TT-004 was completed on December 21. PsA-TT-004 is a Phase 2 study that evaluates the safety and immunogenicity of different dosages and schedules of the MenA conjugate vaccine in 1,200 healthy infants when administered concomitantly with EPI vaccines. The study is conducted at the Navrongo Health Research Centre in Ghana and is scheduled for completion in early 2013.” [10]

On February 4, 2013, Spy News Ghana stated that the research findings show that MenAfriVac is safe and can be given to children under one year old, providing long-term protection from Group-A meningococcal meningitis in this age group. [11]

CONCLUSION

Today, the latest news from Gouro is that 40 children remain paralyzed in hospitals in both Chad and Tunisia, and a further 56 remain ill in the village of Gouro. However, news from Ecoterra International on February 9, 2013, said that the new heath minister wants to send them back home to their ill-equipped village. [12]

Until our intervention, there had been no publicity about the serious vaccine injuries in Chad. However, since our articles were published, there has been a flurry of worldwide media attention, including an extremely biased report in the Guardian UK telling the world that MenAfriVac is a wonderful vaccine. Mind you, to be fair, as you will see from the article, The Bill and Melinda Gates Foundation, a well-known supporter of vaccination initiatives, funded this section of the Guardian. [13]

The whole debacle is one coverup after another. The Chadian government has not asked any independent experts to evaluate the safety and efficacy of the MenAfriVac campaign, stirring up anger among the citizens of Chad. They have been left to cope with extremely sick children, many of whom are still reported to be paralyzed and suffering from severe convulsions. The children need appropriate medical care and their parents deserve answers.

Key

CDC – Centers for Disease Control
FDA – Food and Drug Administration
BMGF – The Bill and Melinda Gates Foundation
PATH – Program for Appropriate Technology in Health
MVP – Meningitis Vaccine Project
WHO – World Health Organization
UNICEF – United Nations International Children’s Emergency Funding

References

1.  http://www.tolerance.ca/Article.aspx?ID=157421&L=en
2.  http://www.sante-tchad.org/Renforcer-les-ressources-humaines-en…
3.  http://vactruth.com/2013/01/13/children-paralyzed-by-vaccine/
4.  http://www.seruminstitute.com/content/products/product_menafrivac.htm
5.  http://www.who.int/immunization_delivery/systems_policy/IPAC_2012_October_report.pdf
6.  http://www.cdc.gov/vaccines/pubs/pinkbook/vac-storage.html#temperatures
7.  http://weatherspark.com/averages/29142/N-Djamena-Chari-Baguirmi-Chad
8.  http://www.treehugger.com/clean-technology/9-countries-have-recorded…
9.  http://www.meningvax.org/clinical-004.php
10. http://www.meningvax.org/files/MVPnewsdigest_2010_Q4_27_EN.pdf
11. http://www.spyghana.com/research-shows-that-new-meningitis-vaccine-is-safe-for-children/
12. http://www.groundreport.com/World/Do-to-them-what-they-are-doing-to-you/2951229
13. http://www.guardian.co.uk/global-development/2013/feb/04/aid-vaccines…

U.S. Government gave $5.7 Billion Given to Vaccine Manufacturers in 2011

By JEFFRY JOHN AUFDERHEIDE | VACTRUTH | DECEMBER 1, 2012

In 2011, the US Federal government awarded 6 pharmaceutical corporations over 5.7 Billion to manufacture children’s vaccines alone.

According to information on the Centers for Disease Control and Federal Business Opportunities websites, the contracts were for the federal Vaccines for Children (VFC) program. [1,2]

The VFC program purchases the vaccines from the vaccine manufacturer. The vaccines are then distributed to state health departments and territorial public health agencies. In turn, children who couldn’t normally afford vaccines are supposed be injected at no cost. [3]

Many vaccine supporters use examples like the VFC program as indisputable proof of kindness on the part of the government and pharmaceutical companies.  I think most parents have heard how generous, caring, and loving they are, haven’t you?

I’d like for you to consider an alternative motive when looking at the contract amounts: a corporate agenda.

Before we get into the individual contract numbers and the corporations who received the money, I’d like to take a moment and share these 4 facts with you:

• Pharmaceutical companies care about profits and shareholders, not your children.[4]

• Since 1989, pharmaceutical companies have paid only 2.3 billion dollars for vaccine injuries. Given the total lifetime care of a vaccine-injured child, many parents believe this figure should be substantially higher.[5]

• The National Childhood Vaccine Injury Act of 1986 (Public Law 99-660) created the National Vaccine Injury Compensation Program (VICP). Vaccine manufacturers (and doctors!) are given complete immunity from any legal liability if your child is harmed by their vaccine(s). No other industry enjoys this level of protection from a product that could injure a child! [6]

• Some of the same pharmaceutical companies listed below have been charged with criminal acts by the Department of Justice.[7]

Click on the image to enlarge.

Contracts and Following the Money

As much as we like to believe we can get something for nothing from Uncle Sam, it’s just not true. There is no such thing as a free lunch. It is simple cause and effect.

While we may never have an opportunity to see into pharma’s accounting books, it is an important step in following the money and seeing who benefits. Here is the contract information I promised earlier in the article.

Company	Contract	Amount
Sanofi Pasteur	200-2011-38199	$1,142,400,000.00 [10]
GlaxoSmithKline	200-2011-38201	$786,456,400.00 [11]
Merck	200-2011-38200	$1,704,454,000.00 [12]
Novartis	200-2011-38204	$451,660,000.00 [13]
Pfizer	200-2011-38203	$1,652,570,000.00 [14]
MassBiologics	200-2011-38202	$11,250,000.00 [15]
Total		$5,748,790,400.00

Are we sure there isn’t some type of corporate agenda?

Read on.

But Vaccine Companies Don’t Make That Much Money, Do They?

It’s a good question to keep asking – and I don’t think it will be solved here.

We may never know the exact amount they profit from vaccines, yet looking into contract amounts is an important step in following the money and seeing who benefits. Look at this important information.

Overall Cost

For example, the World Health Organization website discusses what factors go into establishing vaccine prices. One of the more repeated points you see is:

“Vaccine production costs have a significant fixed cost component, reaching up to 90 percent of total costs. These costs include research and development (R&D), quality control and quality assurance, selling and distribution overhead, and the construction and maintenance of production facilities.” [16]

Let’s assume nothing changes over time – such as increased efficiency in research and development, manufacturing, vaccine tax, etc. – the remaining 10 percent is profit for the pharmaceutical companies.

If we estimate a 10 percent profit from 5.7 billion dollars, this leaves the corporations with an average of 100 million dollars per company.

I have to ask you this question, “Is $100,000,000 a lot of money to you?”

Keep in mind, this is only for the federal Vaccines For Children (VFC) program. The total amount is likely much higher.

Also, do you remember Public Law 99-660 mentioned above? No corporation, corporate executive, board member, doctor, state or local health official can be held responsible for a vaccine injuring your child. Thus, Big Pharma’s profits from manufacturing vaccines are very safe.

Well played, Big Pharma.

Here’s the Bottom Line: Pharma Gets a Free Meal Ticket

What is really happening is the US Federal government has given the corporations a guaranteed paycheck through the contracts. It makes perfect sense why the federal health agencies would keep demanding more vaccinations – they get more money!

Take the example of the former head of the Centers for Disease Control (CDC), Julie Gerberding. She helped promote the highly controversial Gardasil vaccine while she served in her government post. After she finished working for the CDC, she was made President of the Vaccine Division for Merck Pharmaceuticals.

To illustrate my point, I created a simple summary of one way money pours into the pharmaceutical company’s coffers.

 

Click on the image to enlarge.

When government money is given to corporations, we have to start looking at the individual humans who serve them.

Here’s one perspective from a legendary American trial lawyer, Gerry Spence, as he describes corporations as:

“… not a human being. It is not a group of human beings. Remember that. It is a fictional structure. A form – a nonliving, nonbreathing, nonhuman form – an invisible form…I have heard many a corporate executive argue that he has no loyalty to his employees, to his customers, or to his country. His loyalty, all of it, is to the profit of his shareholders.”[8,9]

Indeed, the love of money (greed) is a very common human attribute and becomes a problem as in the case of pharmaceutical giant Pfizer.

They were charged by the Department of Justice with payments to influence government officials. In turn, Pfizer was ‘fined’ 40 million dollars.

Put in context, it is about 2.5 percent of the grant money given to them by the CDC for making vaccines. [7] It’s a pity that laws passed by the same politicians are not overturned when this type of tomfoolery is uncovered.

But that game is well-understood by Pharma, is it not?

Conclusion

If your child is harmed by vaccines, you should know your hands are legally tied.

Through public law, these corporations have been made too big to fail, just like the banks. They make a hefty profit from government contracts. It’s a guaranteed paycheck for them – there is no incentive to change the process.

We must remember the pharmaceutical companies are in business to make profits and ensure shareholder value. I recently shared a graphic on the VacTruth.com Facebook page which sums up how I feel, “The pharmaceutical industry does not create cures, they create customers.”

Tip for Readers

If you want to look up the award amounts for yourself, follow these 3 easy steps.

1. Go to https://www.fbo.gov/index?s=opportunity&mode=list&tab=archives
2. Copy and Paste one of the contract numbers listed above (Ex. “200-2011-38199”) into the “Keyword / Solicitation #” field.
3. In the “Posted Date” field, make sure the ‘blank’ value is selected. It is above the “Today”.  You should get a result similar to what is

References

1. http://www.cdc.gov/vaccines/pubs/acip-list.htm

2.  https://www.fbo.gov/

3.  http://www.cdc.gov/vaccines/programs/vfc/index.html

http://www.novartis.com/about-novartis/our-mission/index.shtml

Part of a mission statement from one pharmaceutical company states, “We also want to provide a shareholder return that reflects outstanding performance and to adequately reward those who invest ideas and work in our company.”

This language is not uncommon in corporate mission statements – even for pharmaceutical companies.

5. http://www.hrsa.gov/vaccinecompensation/statisticsreports.html#claimscompensated

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

7. http://vactruth.com/2012/08/28/pharma-admits-to-bribes/

8. Spence, Gerry. (1995). How to Argue and Win Every Time. St. Martin’s Press. Pg 270.

9. Ilbid., Pg 281.

10. Contract Award for Sanofi Pasteur

https://www.fbo.gov/index?s=opportunity&mode=form&tab=core&id=9c6e25873f0cdaa9220b6f9a4d3f59e0

11. Contract Award for GlaxoSmithKline

https://www.fbo.gov/index?s=opportunity&mode=form&id=8d9318e0064e03d202bd4e82201fba56&tab=core&_cview=0

12. Contract Award for Merck

https://www.fbo.gov/index?s=opportunity&mode=form&id=d0f96e01f7c99849184ebae2280d47cf&tab=core&_cview=0

13. Contract Award for Novartis

https://www.fbo.gov/index?s=opportunity&mode=form&id=c4bfebe64d04bd0a9342fd51d736fd77&tab=core&_cview=0

14. Contract Award for Pfizer

https://www.fbo.gov/index?s=opportunity&mode=form&id=81727165b87a75be1ed4d24b292e3fda&tab=core&tabmode=list&=

15. Contract Award for Mass Biologics

https://www.fbo.gov/index?s=opportunity&mode=form&id=bb75e52010be266964a8992c2d21c43c&tab=core&_cview=0

16. http://www.who.int/immunization_financing/options/en/briefcase_vacproduction.pdf

Fetal Deaths up 4000% after pregnant mothers took Flu Vaccine

CDC had recommended the double-dosing of the pregnant population with the seasonal flu vaccine with mercury and the untested H1N1 vaccine with mercury.

By CHRISTINA ENGLAND | VACTRUTH | NOVEMBER 26, 2012

Documentation received from the National Coalition of Organized Women (NCOW) states that between 2009 and 2010 the mercury-laden combined flu vaccinations have increased Vaccine Adverse Events Reporting Systems (VAERS) fetal death reports by 4,250 percent in pregnant women. Eileen Dannemann, NCOW’s director, made abundantly clear that despite these figures being known to the Centers for Disease Control (CDC), the multiple-strain, inactivated flu vaccine containing mercury (Thimerosal) has once again been recommended to pregnant women as a safe vaccination this season.

Outraged by the CDC’s total disregard for human life, Ms. Dannemann accused the CDC of ‘willful misconduct,’ saying that they are responsible for causing the deaths of thousands of unborn babies. She stated that the CDC deliberately misled the nation’s obstetricians and gynecologists and colluded with the American Journal of Obstetrics and Gynecology (AJOG) to mislead the public by advertising the flu vaccine as a safe vaccine for pregnant women when they knew fully well that it was causing a massive spike in fetal deaths.

In a letter to Dr. Joseph Mercola, Ms. Dannemann wrote:

“Not only did the CDC fail to disclose the spiraling spike in fetal death reports in real time during the 2009 pandemic season as to cut the fetal losses, but also we have documented by transcript Dr. Marie McCormick, chairperson of the Vaccine Safety Risk Assessment Working Group (VSRAWG) on September 3, 2010, denying any adverse events in the pregnant population during the 2009 Pandemic season.” [1]

HIDING LIFE-OR-DEATH EVIDENCE

Because the H1N1 pandemic vaccine had never been tested on the pregnant population, and to lessen the intensity of fears of the unknown risks, Dr. Marie McCormick of the CDC was employed to keep track of all adverse events during the 2009 pandemic season, including those adverse events in the pregnant population. Dr. McCormick was responsible for sending monthly reports to the Secretary of the Health and Human Services (HHS), citing any suspicious adverse events.

According to Ms. Dannemann, NCOW has been unable to obtain access to these monthly reports. After sending a Freedom of Information Act request to the CDC, she was told that she may have to wait 36 months to access what should be published public reports.

The Mercola letter continues:

“The Advisory Committee on Childhood Vaccines (ACCV) and CDC were confronted with the VAERS data from NCOW on September 3, 2010, in Washington, D.C., and then again by conference call on September 10, and then again in Atlanta, Georgia, on October 28, 2010. On both September 3 and September 10^, Dr. Marie McCormick clearly denied that there were any adverse events for pregnant women from the 2009 flu vaccine.”

THE DOCTOR’S VERSION OF CONCEAL AND CARRY

To emphasize their point, on October 28, 2010, NCOW requested that Dr. Rene Tocco present their data at the CDC headquarters in Atlanta, Georgia. The CDC’s Dr. Shimabakuru gave a presentation on significant adverse reactions to the H1N1 vaccine, such as cases of Guillane-Barre Syndrome, which appeared to have risen three percent, claiming it as an insignificant signal.

No mention at all was made of adverse events related to pregnant women. Unfortunately for Dr. Shimabakuru, his attempts to pull the wool over the eyes of the audience were foiled when he was challenged by a member of the audience asking if the vaccine caused adverse events in pregnancy. Feeling cornered, he reluctantly looked in his bag and sheepishly presented a slide that corroborated the NCOW data, confirming that the CDC knew of the spike in fetal deaths in the fall of 2010. [2]

So, why did Dr. Shimabkauru have a slide containing compromising evidence in his bag? Why did he decide to hide the slide? Surely, if he had prepared a slide outlining this crucial data, it would have made sense to include the slide in his presentation. After all, a 4,250 percent increase in fetal deaths is far more significant that a three percent increase in Guillane-Barre Syndrome.

Ms. Dannemann believes that the existence of this slide, along with the omission of it in his presentation, confirms that the CDC knew of the spike in fetal deaths by the fall of 2010 and was attempting by any means possible not to make it public.

Outlining a catalog of events, Ms. Dannemann believes the CDC’s continual cover ups puts the lives of pregnant women and their unborn children in serious jeopardy. She maintained:

“Continuing the vaccine program without notifying the public or the healthcare practitioners of the VAERS miscarriage/stillbirth incoming data was clearly a purposeful decision. The CDC, aware of their own incoming stream of early vaccine adverse events reports, clearly decided to allow the obstetricians to continue, unwittingly, murdering and damaging the unborn so that the CDC’s blunder of recommending the double-dose vaccination of pregnant women could be kept under the radar.”

COLLABORATION AND CORRUPTION

Despite evidence that the CDC knew of the 4,250 percent increase in fetal death reports in 2009/2010, in order to ensure the continuance of the vaccine program for pregnant women, the CDC published a study in AJOG authored by Dr. Pedro Moro of the CDC in the fall of 2010. The study articulated that there were only 23 miscarriages caused by the single flu vaccine in 19 years between 1990 – 2009, an average of 1.2 miscarriages per year. This study formed the basis of a CDC worldwide publicity campaign that the flu shot was safe for pregnant women by willfully and strategically excluding the 2009 pandemic data, which was available to them. Ms. Dannemann said:

“Both the CDC and AJOG were well aware of the fact that physicians and the public were awaiting the results of the 2009 H1N1 untested vaccine on pregnant women, amid solid assurances to the public at the beginning of the pandemic season that the CDC was on top of collecting any adverse reactions to the vaccine by establishing the Vaccine Safety Risk Assessment Working Group chaired by Dr. Marie Mc Cormick (VSRAWG).”

Ms. Dannemann stated that by including the 2008/2009 flu season’s data but excluding the available 2009 data from the 2009/2010 flu season in the study published in AJOG, Dr. Moro was able to give the impression that the 2009/2010 pandemic season was covered in the data, which of course it was not. Ms. Dannemann believes that this was a deliberate act on his part because he was aware of the fetal death spike in the 2009/2010 data at the time of preparing the study and purposely excluded the 2009 pandemic data from the study to hide this fact.

In the fall of 2010, just in time for the new flu season, media outlets all over the world publicized the AJOG, peer-reviewed CDC/Dr. Moro study as adamant proof that the flu shot is safe for pregnant women. The NCOW documents prove at the same time as widely publicizing advice that all pregnant women required the combined flu vaccination, the CDC was busy organizing ten non-profit organizations, to sign a joint letter to urge obstetricians and gynecologists to continue to vaccinate their pregnant patients.

One of the organizations to sign the letter was The March of Dimes [3] who urged health care providers to recommend the flu vaccine to pregnant women and those who expect to become pregnant. They wrote the following recommendation to all medical professionals:

“Advice from a healthcare provider plays an important role in a pregnant and postpartum woman’s decision to get vaccinated against seasonal influenza. The American Academy of Family Physicians (AAFP), American Academy of Pediatrics (AAP), American College of Nurse-Midwives (ACNM), American College of Obstetricians and Gynecologists (The College), American Medical Association (AMA), American Nurses Association (ANA), American Pharmacists Association (APhA), Association of Women’s Health, Obstetric and Neonatal Nurses (AWHONN), March of Dimes, and Centers for Disease Control and Prevention (CDC) are asking for your help in urging your pregnant and postpartum patients to get vaccinated against seasonal influenza.

The Advisory Committee on Immunization Practices (ACIP) recommends that pregnant and postpartum women receive the seasonal influenza vaccine this year, even if they received 2009 H1N1 or seasonal influenza vaccine last year. Lack of awareness of the benefits of vaccination and concerns about vaccine safety are common barriers to influenza vaccination of pregnant and postpartum women.”

Representatives from all ten organizations signed the letter.

WHAT THE CDC FAILED TO TELL PREGNANT MOMS

This year, on September 27, 2012, the Human and Environmental Toxicology Journal (HET) published Dr. Gary Goldman’s study that confirms NCOWs data, a 4,250 percent increase in the number of miscarriages and stillbirths reported to VAERS in the 2009/2010 flu season. [4] The study points out an astounding fact that no one saw until the publishing of the Goldman study in HET: the CDC had recommended the double-dosing of the pregnant population with the seasonal flu vaccine with mercury and the untested H1N1 vaccine 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.”

The facts that Goldman exposed are extremely disturbing. He highlights the fact that the safety and effectiveness of the A-H1N1 had never been established in pregnant women and that the combination of two different influenza vaccines had never been tested on pregnant women at all.

Even more worrisome is the fact that the A-H1N1 vaccine inserts from the various manufacturers contained this warning:

“It is also not known whether these vaccines can cause fetal harm when administered to pregnant women or can affect reproduction capacity.’’ (emphasis added)

Dr. Goldman also pointed out that the developing fetus is indirectly exposed to mercury when thimerosal-containing vaccines are administered to a pregnant woman. He outlined a study written by A.R. Gasset, M. Itoi, Y. Ischii and R.M. Ramer who examined what happened after rabbits were vaccinated with thimerosal–containing radioactive mercury. Goldman stated that from one hour post-injection to six hours post-injection, the level of radioactive mercury in the blood dropped over 75 percent. Yet from two hours post-injection to six hours post-injection, there were significantly increased radioactivity levels in the fetal brain, liver, and kidney.

Dr. Goldman concluded that because the rates of miscarriage reported to the Vaccine Adverse Events Reporting System (VAERS) for the single flu vaccine were relatively low, health care providers developed a false sense of security that flu vaccines administered during pregnancy were safe.  Goldman explained that just because a single vaccine has been tested and considered to be relatively safe, this does not mean that vaccinating pregnant women with two or more Thimerosal containing vaccines will be safe for them or their unborn babies. Overall, Goldman firmly believes that the VAERS grossly underestimates the true rates of miscarriage and other adverse events encountered in the US population. Remember, it is estimated that  less than a tenth of true adverse reactions are reported to the VAERS with a one percent reporting rate for serious adverse events, including death, according to a study led by former FDA Commissioner Dr. David A. Kessler. [5]

As seen in the Goldman study, with the return to a single flu shot, the flu vaccine-related reports of fetal loss have returned to a significantly lower level compared to the high level of fetal loss reports in the two-dose 2009/2010 flu season. However, higher than background flu shot vaccine-related fetal losses continue to be reported to the VAERS.

Furthermore, the Goldman study recommends that the babies who survived the deadly double dose in utero be monitored:

“In addition, because of the order of magnitude increase in fetal-loss report rates, from 6.8 fetal loss reports per million pregnant women vaccinated in the single-dose 2008/2009 season to 77.8 in the two-dose 2009/2010 season, further long term studies are needed to assess adverse outcomes in the surviving children. Additional research concerning potential synergistic risk factors associated with the administration of Thimerosal-containing vaccines is warranted, and the exposure-effect association should be verified in further toxicological and case-control studies.” (emphasis added)

Aside from fetal deaths, the CDC initiative to increase uptake of vaccines in pregnant women continues to fuel the increases in the levels of neurodevelopmental, developmental, behavioral abnormalities, and chronic illness in the surviving children. Due to omitting reports of fetal deaths, the CDC enjoys success in increasing the uptake and number of vaccines in the pregnant population. The Advisory Committee on Immunization Practices (ACIP) is now recommending not only the flu shot (with mercury) but also the Tdap vaccine.

CONCLUSION

The work of NCOW and Dr. Goldman has proven that potential lives are being destroyed before they are even old enough to draw their first breath. Developing fetuses who are fortunate enough to survive the onslaught of vaccinations now being recommended to pregnant women then need to play a form of Russian Roulette from the day they are born, because their caring parents followed the advice they were given by professionals who have been deliberately misguided.

Eileen Dannemann and her team have proven with their remarkable work that both public and professionals alike are being lied to and deceived by organizations put in place by the government to sanction our vaccination programs. In my opinion, this is genocide and the sooner people realize that all vaccines come with an element of risk and begin to research the dangers for themselves, the sooner these insane experiments will end.

References

1. Official transcript CDC’s Dr. Marie McCormick denies miscarriages, Sept. 3, 2010 ACCV. See page 37.
2. Influenza Vaccine Safety Monitoring (slide 20).
   CDC’s Dr. Tom Shimabukuro confirms NCOW data , Oct. 28, 2010 ACIP
3. Letter from March of Dimes, inlcuded in this article.
4. Dr Gary Goldman Comparison of VAERS fetal-loss reports during three consecutive influenza seasons: Was there a synergistic fetal toxicity associated with the two-vaccine 2009/2010 season? http://het.sagepub.com/content/early/2012/09/12/0960327112455067.abstract?rss=1 (abstract only)
5. Kessler, D.A. The Working Group. Natanblut, S. Kennedy, D. Lazar, E. Rheinstein, P. et al. Introducing MedWatch: A New Approach to Reporting Medication and Device Adverse Effects and Product Problems. JAMA 1993 June 2. 269 (21): 2765-2768.

Flu Shot Linked to H1N1 Pandemic

By HELEN BRANSWELL | CANADIAN PRESS | SEPTEMBER 10, 2012

A strange vaccine-related phenomenon spotted in Canada at the start of the 2009 flu pandemic may well have been real, a new study suggests.

Researchers, led by Vancouver’s Dr. Danuta Skowronski, an influenza expert at the B.C. Centre for Disease Control, noticed in the early weeks of the pandemic that people who got a flu shot for the 2008-09 winter seemed to be more likely to get infected with the pandemic virus than people who hadn’t received a flu shot.

Five studies done in several provinces showed the same unsettling results. But initially research outside Canada did not, and the effect was dismissed as a “Canadian problem,” a problem with the flu vaccine used in Canada.

But a new study suggests the findings were real.

Skowronski and a group of researchers have recreated the event in ferrets. Their findings were presented Sun-day at the Interscience Conference on Antimicrobial Agents and Chemotherapy, a major international infectious diseases conference taking place in San Francisco.

Skowronski, who outlined the work at a webcast press conference, worked with 32 ferrets, giving half the 2008 seasonal flu shot and the rest a placebo injection. The work was blinded, meaning the researchers didn’t know which ferrets received which shot. Later, all the ferrets were infected with the pandemic H1N1 virus.

The ferrets in the vaccine group became significantly sicker than the other animals, though all recovered.

“The findings are consistent with the increased risk that we saw in the human studies,” Skowronski said.

The reason is unclear and Skowronski urged other research groups to take up the question. She said it’s important to get to the root before the next pandemic. But in the meantime, Skow-ronski insisted the findings should not deter people from getting flu shots.