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Showing posts with label vaccine. Show all posts
Showing posts with label vaccine. Show all posts

Sunday, June 06, 2010

WHO scandal exposed: Advisors received kickbacks from H1N1 vaccine manufacturers

WHO scandal exposed: Advisors received kickbacks from H1N1 vaccine manufacturers

A stunning new report reveals that top scientists who convinced the World Health Organization (WHO) to declare H1N1 a global pandemic held close financial ties to the drug companies that profited from the sale of those vaccines. This report, published in the British Medical Journal, exposes the hidden ties that drove WHO to declare a pandemic, resulting in billions of dollars in profits for vaccine manufacturers.

Several key advisors who urged WHO to declare a pandemic received direct financial compensation from the very same vaccine manufacturers who received a windfall of profits from the pandemic announcement. During all this, WHO refused to disclose any conflicts of interests between its top advisors and the drug companies who would financially benefit from its decisions.

All the kickbacks, in other words, were swept under the table and kept silent, and WHO somehow didn't think it was important to let the world know that it was receiving policy advice from individuals who stood to make millions of dollars when a pandemic was declared.

WHO credibility destroyed

The report was authored by Deborah Cohen (BMJ features editor), and Philip Carter, a journalist who works for the Bureau of Investigative Journalism in London. In their report, Cohen states, "...our investigation has revealed damaging issues. If these are not addressed, H1N1 may yet claim its biggest victim -- the credibility of the WHO and the trust in the global public health system."

In response to the report, WHO secretary-general Dr Margaret Chan defended the secrecy, saying that WHO intentionally kept the financial ties a secret in order to "...protect the integrity and independence of the members while doing this critical work... [and] also to ensure transparency."

Dr Chan apparently does not understand the meaning of the word "transparency." Then again, WHO has always twisted reality in order to serve its corporate masters, the pharmaceutical giants who profit from disease. To say that they are keeping the financial ties a secret in order to "protect the integrity" of the members is like saying we're all serving alcohol at tonight's AA meeting in order to keep everybody off the bottle.

It just flat out makes no sense.

But since when did making sense have anything to do with WHO's decision process anyway?

Even Fiona Godlee, editor of the BMJ, had harsh words for the WHO, saying, "...its credibility has been badly damaged. WHO must act now to restore its credibility."

Yet more criticism for WHO

The BMJ isn't the only medical publication criticizing WHO for its poor handling of conflicts of interest. Another report from the Council of Europe Parliamentary Assembly also criticized WHO, saying: "Parliamentary Assembly is alarmed about the way in which the H1N1 influenza pandemic has been handled, not only by the World Health Organization (WHO), but also by the competent health authorities at the level of the European Union and at national level." It went on to explain that WHO's actions led to "a waste of large sums of public money, and also unjustified scares and fears about health risks faced by the European public at large."

The funny thing is, NaturalNews and other natural health advocates told you all the same thing a year ago, and we didn't have to spend millions of dollars on a study to arrive at this conclusion. It was obvious to anyone who knows just how corrupt the sick-care industry really is. They'll do practically anything to make more money, including bribing WHO scientific advisors and paying them kickbacks once the vaccine sales surge.

The vaccine industry and all its drug pushers are, of course, criticizing this investigative report. They say WHO "had no choice" but to declare a pandemic and recommend vaccines, since vaccines are the only treatment option for influenza. That's a lie, of course: Vitamin D has been scientifically proven to be five times more effective than vaccines at preventing influenza infections, but WHO never recommended vitamin D to anyone.

The entire focus was on pushing more high-profit vaccines, not recommending the things that would actually help people the most. And now we know why: The more vulnerable people were to the pandemic, the more would be killed by H1N1, thereby "proving" the importance of vaccination programs.

People were kept ignorant of natural remedies, in other words, to make sure more people died and a more urgent call for mass vaccination programs could be carried out. (A few lives never gets in the way of Big Pharma profits, does it?)

How the scam really worked

Here's a summary of how the WHO vaccine scam worked:

Step 1) Exaggerate the risk: WHO hypes up the pandemic risk by declaring a phase 6 pandemic even when the mortality rate of the virus was so low that it could be halted with simple vitamin D supplements.

Step 2) Urge countries to stockpile: WHO urged nations around the world to stockpile H1N1 vaccines, calling it a "public health emergency."

Step 3) Collect the cash: Countries spend billions of dollars buying and stockpiling H1N1 vaccines while Big Pharma pockets the cash.

Step 4) Get your kickbacks: WHO advisors, meanwhile, collected their kickbacks from the vaccine manufacturers. Those kickbacks were intentionally kept secret.

Step 5) Keep people afraid: In order to keep demand for the vaccines as high as possible, WHO continued to flame the fears by warning that H1N1 was extremely dangerous and everybody should continue to get vaccinated. (The CDC echoed the same message in the USA.)

This is how WHO pulled off one of the greatest vaccine pandemic scams in the last century, and it worked like gangbusters. WHO advisors walked away with loads of cash, the drug companies stockpiled huge profits, and the taxpayers of nations around the world were left saddled with useless vaccines rotting on the shelves that will soon have to be destroyed (at additional taxpayer cost, no doubt) or dumped down the drain (where they will contaminate the waterways).

Meanwhile, nobody dared tell the public the truth about vitamin D, thereby ensuring that the next pandemic will give them another opportunity to repeat the exact same scam (for yet more profit).

The criminality of the vaccine industry

The bottom line is all this is a frightening picture of just how pathetic the vaccine industry has become and how corrupt the WHO and the CDC really are. What took place here is called corruption and bribery, folks. Kickbacks were paid, lies were told and governments were swindled out of billions of dollars. These are felony crimes being committed by our global health leaders.

The real question is: Why do governments continue to allow public health organizations to be so easily corrupted by the vaccine industry? And who will stand up to this profit conspiracy that exploits members of the public as if they were profit-generating guinea pigs?

The next time you hear the WHO say anything, just remember: Their advisors are on the take from the drug companies, and just about anything you're likely to hear from the World Health Organization originates with a profit motive rather than a commitment to public health.

Oh, and by the way... for the record, there has never been a single scientific study ever published showing that H1N1 vaccines worked. Not only was the H1N1 pandemic a fraud to begin with, but the medicine they claimed treated it was also based on fraud. And now we know the rest of the story of why it was all done: Kickbacks from Big Pharma, paid to advisors who told WHO to declare a pandemic.

Sources for this story include:

http://abcnews.go.com/Health/SwineF...

http://www.washingtonpost.com/wp-dy...

Thursday, June 03, 2010

Consuming Chemicals : Rethinking What We Heat, Serve and Eat (By Sarah (Steve) Mosko, Ph.D.)

Consuming Chemicals : Rethinking What We Heat, Serve and Eat (By Sarah (Steve) Mosko, Ph.D.)

What do breast milk, food cans, microwave popcorn, and fast-food French fry boxes have in common with meat, fish and dairy products? They’re all avenues of human ingestion of potentially harmful chemicals associated with everyday plastics.

BPA is a key ingredient of the epoxy resin that lines metal food cans and jar lids.
Although the jury is still out on what levels of exposure are unsafe, it is indisputable that we all consume chemicals from plastics on a daily basis.

Biomonitoring projects like Environmental Working Group’s 2005 BodyBurden study of cord blood in neonates and the Mind, Disrupted investigation of blood and urine in adults representing the learning and developmental disabilities community published in February 2010—consistently find neurotoxic and endocrine-disrupting chemicals used in common plastics among the substances routinely tainting human tissues. Although diet is not the only route of exposure, it is a major one.

Given that developing fetuses and young children are most vulnerable to environmental toxins, understanding how exposure occurs through ordinary diets, and how to avoid it, has become a growing societal concern.

Three constituents of common plastics that find their way into food or drinks are described below, all linked to ill health effects in humans and lab animals. In the Mind, Disrupted study, the subjects universally tested positive for all three: bisphenol-A, brominated flame retardants, and perfluorinated compounds. The variety of avenues into the human diet is surprising.

Bisphenol-A

Originally synthesized a century ago as a synthetic estrogen, bisphenol-A (BPA) was utilized instead to make baby bottles, reusable water bottles, and food storage containers upon discovery that polymerization produced clear, shatter-proof plastics dubbed polycarbonates. It’s also a key ingredient of the epoxy resin that lines metal food cans and jar lids, including infant formula.

Over 90% of Americans have BPA in their urine, according to the 2003–2004 National Health and Nutrition Examination Survey (NHANES) of the U.S. population. Young children generally have the highest levels because they lack an enzyme that breaks down BPA. Leaching of BPA from containers into food and beverages is thought to be the main route of exposure.

The U.S. Environmental Protection Agency (EPA) set a now outdated safe exposure standard of <50ug/kg/day>

Responding to the newer findings, the National Toxicology Program Center for the Evaluation of Risks to Human Reproduction released a monograph in September 2008 admitting “some concern” that current levels of exposure in fetuses, infants and children may result in developmental changes in the brain, prostate and behavior. In January 2010, the U.S. Food and Drug Administration posted its support for voluntary moves by industry to both stop selling BPA-containing baby bottles and feeding cups and develop alternatives to BPA-lined infant formula cans, but it stopped short of recommending bans on BPA or that parents change use of infant formula or foods.

Only Connecticut, Minnesota and Wisconsin have passed laws banning BPA in children’s foodware and drinkware.

Brominated Flame Retardants

Polybrominated diphenyl ethers (PBDEs) are a family of flame retardants in widespread use in consumer products, including plastics for electronics and electrical devices. Because PBDEs are not permanently bonded to the plastic polymers, they migrate out into the environment.

Properties of PBDEs include resistance to biodegradation and affinity for fats, allowing them to persist in the environment and bioaccumulate in the food web. PBDEs were found in nearly 100% of blood samples in the 2003-2004 NHANES survey. Consumption of meat, fish and dairy products is thought to be a primary route of exposure.

However, it was the discovery of infant exposure to PBDEs via rising levels in human breast milk in the United States and Europe that set off a chorus of alarm about health risks to humans.

PBDEs have been marketed in the United States in three commercial mixtures, so-called penta, octa and deca formulations. Because of animal data linking penta and octa to serious health impairments—including liver, thyroid and reproductive toxicity and especially developmental neurotoxicity—domestic manufacture of penta and octa was voluntarily phased out in 2004. However, levels of penta and octa in humans continue to rise, attributable in part to widespread use of deca which can break down into other forms.

In December 2009, the EPA outlined an action plan to reduce human exposure to PBDEs which recommended only a voluntary phase out of deca in lieu of a federal restriction. California is among 11 states that have enacted bans on penta and octa.

However, even public health-advocacy organizations that support phase-out of all PBDEs, like Environmental Working Group, do not recommend that parents stop breastfeeding because of breastfeeding’s positive impact on other measures of infant well-being.

Perfluorinated Compounds

Perfluorinated Compounds (PFCs) are synthetic polymers that find their way into food applications because they repel oils and water. They are the key ingredient of grease/water-resistant coatings on non-stick cookware (e.g. Teflon®), pizza boxes, microwave popcorn, and fast-food wrappers.

The most studied PFCs are PFOA (perfluorooctanoate) and PFOS (perfluorooctanesulfonate) which are known to persist seemingly indefinitely once released into the environment and consequently build up in the food web. They also persist in human tissues: The half-life of PFOA and PFOS in human blood is roughly four to five years, according to a 2007 study of retirees of a PFC manufacturing facility.

Ninety-eight percent of the blood samples in the 2003-2004 NHANES project contained PFOA and PFOS. Breast milk contaminated with PFOA and PFOS was detected in 98% of Massachusetts women participating in a 2004 study. Dietary intake of meat, fish and dairy products is thought to be a major route of exposure along with consumption of foods contaminated through contact with grease/water-resistant packaging (e.g. fast foods).

Non-stick cookware, when heated to high temperatures, has also been shown to release substances that might taint foods per tests performed by Environmental Working Group.

The list of potential health effects linked to PFCs in human and animals studies is long and includes cancers, high cholesterol, liver and developmental toxicity, thyroid hormone disruption and infertility.

No U.S. jurisdiction has yet limited the used of PFOA or PFOS in food contact substances.

CONTACT: Mind, Disrupted.

SARAH (STEVE) MOSKO, PH.D., is an environmental writer living in California who blogs at Boogie Green


Friday, May 28, 2010

Bill Gates funds covert vaccine nanotechnology

Bill Gates funds covert vaccine nanotechnology

natural health

Bill Gates funds covert vaccine nanotechnology

Friday, May 28, 2010
by Mike Adams, the Health Ranger
Editor of NaturalNews.com (See all articles...)
NaturalNews) The Bill and Melinda Gates Foundation is gaining a reputation for funding technologies designed to roll out mass sterilization and vaccination programs around the world. One of the programs recently funded by the foundation is a sterilization program that would use sharp blasts of ultrasound directed against a man's scrotum to render him infertile for six months. It might accurately be called a "temporary castration" technology. Read more about it here: http://www.naturalnews.com/028853_u...

Now, the foundation has funded a new "sweat-triggered vaccine delivery" program based on nanoparticles penetrating human skin. The technology is describes as a way to "...develop nanoparticles that penetrate the skin through hair follicles and burst upon contact with human sweat to release vaccines."

The research grant money is going to Carlos Alberto Guzman of the Helmholtz Centre for Infection Research in Germany and Claus-Michael Lehr and Steffi Hansen of the Helmholtz-Institute for Pharmaceutical Research.

These are both part of the Gates Foundation's involvement in the "Grand Challenges Explorations" program which claims to be working to "achieve major breakthroughs in global health."

...breakthroughs like mass sterilization and nanoparticle vaccines that could be covertly administered even without your knowledge, it turns out. These nanoparticles could be used in a spray mist that's sprayed on to every person who walks through an airport security checkpoint, for example. Or it could be unleashed through the ventilation systems of corporate office buildings or public schools to vaccinate the masses. You wouldn't even know you were being vaccinated.

This technology is potentially very dangerous to your health freedom. Using it, governments or drug companies (which are all the same thing these days) could create a vaccine skin cream that's handed out and described as "sunscreen." But when you put it on, you're actually vaccinating yourself as the nanoparticles burrow underneath your skin and burst, releasing foreign DNA inside your body.

A history of covert mass medication

But why would the government medicate people without their knowledge or consent, you ask? They already do it with water fluoridation. Fluoride is a drug, and regional and national governments all over the world are using the water supply as a way to deliver the fluoride drug to people whether they need it or not -- and without any proper medical diagnosis or prescription.

So if governments are already covertly medicating people with fluoride in the water supply, they've set the stage mass-vaccinating people through similar channels, such as the air supply in buildings. And thanks to Bill Gates, this nanotechnology needed to pull this off is now being funded.

Is this really a "major breakthrough in global health?"

I suppose it is if you believe in covert medicine where you dose people with drugs or vaccines without their knowledge. Western medicine is so offensive to rational people that it can't even operate out in the open. That's why it resorts to covert contamination of the water supply in order to force the public to swallow its drugs.

Fluoride and covert medicine

Oh, by the way, to anyone who argues that fluoride is not a drug, remember this: According to the FDA, any chemical substance that has a biological effect on the human body is, by definition, a drug. Therefore fluoride is a drug, too.

Even more, fluoride is promoted with outlandish claims about "preventing cavities" by swallowing it, making it an "unapproved drug" according to the FDA. So how is it that this unapproved drug can be dripped into the water supply and forced upon hundreds of millions of people without a single diagnosis of fluoride deficiency or even a single prescription from a doctor?

The answer is that western medicine is so arrogant that it does not believe it needs to follow any rules, regulations or laws. It is a system of "bully" medicine where drugs are shoved down your throat by being covertly dripped into the water supply without your consent. So why should we believe vaccines will be any different? If mainstream medicine can find a way to force every person to unknowingly be injected with vaccines, make no mistake they will pursue it!

And such efforts will no doubt have the continued financial support of Bill Gates.

Saturday, May 01, 2010

ADD and ADHD Fraud. Find out the truth about ADD and ADHD. Exposing the Fraud of ADD and ADHD.

ADD and ADHD Fraud. Find out the truth about ADD and ADHD. Exposing the Fraud of ADD and ADHD.: "'They made a list of the most common symptoms of emotional discomfiture of children; those which bother teachers and parents most, and in a stroke that could not be more devoid of science or Hippocratic motive--termed them a 'disease.' Twenty five years of research, not deserving of the term 'research.,' has failed to validate ADD/ADHD as a disease. Tragically--the 'epidemic' having grown from 500 thousand in 1985 to between 5 and 7 million today--this remains the state of the 'science' of ADHD.'

In addition to scientific articles that have appeared in leading national and international medical journals, Dr. Baughman has testified for victimized parents and children in ADHD/Ritalin legal cases, writes for the print media and appears on talk radio shows, always making the point that ADHD is fraudulent--a creation of the psychiatric-pharmaceutical cartel, without which they would have nothing to prescribe their dangerous, addictive, Schedule II, stimulants for--namely, Ritalin (methylphenindate), Dexedrine (dextro-amphetamine), Adderall (mixed dextro- and levo-amphetamine) and, Gradumet, and Desoxyn (both of which are methamphetamine, 'speed,' 'ice').

The entire country, including all 5-7 million with the ADHD diagnosis today, have been deceived and victimized; deprived of their informed consent rights and drugged--for profit! It must be stopped. Now!"

Tuesday, April 27, 2010

The Five Best Anti-Viral Products to Beat Influenza, Swine Flu, Bird Flu and SARS page 0

The Five Best Anti-Viral Products to Beat Influenza, Swine Flu, Bird Flu and SARS page 0: "
(NaturalNews) This is a special report the FDA doesn't want you to read. In fact, this is the story that the corporate "leaders" of the natural health products industry don't want you to read, either. Why? Because they've all been hijacked by Big Pharma interests, and they no longer represent real natural medicine like the kind revealed in this story. Read more about this consumer betrayal by the natural products industry leaders here: http://www.naturalnews.com/026215.html

When it comes to H1N1 influenza (Swine Flu), all the "authority" institutions in America agree on one thing: Keep the American people ignorant! Don't allow people to learn the truth about the anti-viral properties of herbs, superfoods and dietary supplements.

Knowledge is a dangerous thing. It gives people options. It allows people to be independent from the government and independent from the medical system. It gives people control over their own lives, and in a police state society that seeks to dominate the health decisions of every citizen (http://www.naturalnews.com/026305.html), giving people control over their own lives simply cannot be tolerated.

That's why this article will be blasted as "irresponsible" by health authorities. It will be portrayed as "dangerous" by pharmaceutical pushers. If the FDA could ban this website, this article would be precisely the kind of content they would target for censorship.

And what's so dangerous about this article? It dares to advocate specific anti-viral products as protection against the H1N1 swine flu.

NEXT PAGE: Why modern medicine will fail us in the next great pandemic...

Two Ways to Get Prepared Now for the Next Pandemic:

• Audio program: How to Prepare For and Survive Any Pandemic featuring Dr. Sheldon Marks and the Health Ranger. Covers emergency medical preparedness and more.

• The Swine Flu Advanced Preparedness Course with the Health Ranger, including Q&A from readers. Includes powerful strategies for protecting you and your family from any pandemic.



Friday, April 16, 2010

Life-Cycle Studies: High-Fructose Corn Syrup | Worldwatch Institute

Life-Cycle Studies: High-Fructose Corn Syrup | Worldwatch Institute:

Life-Cycle Studies: High-Fructose Corn Syrup

by Ben Block on April 9, 2010

Corn syrup labelPhoto courtesy Archives of Ontario

Early 20th-century label." class="caption" align="" height="207" width="250">

Photo courtesy Archives of Ontario

Early 20th-century label.
For the past five years, Worldwatch has explored the history, production method, and environmental and social impacts of everyday products - from chopsticks to pencils - in the Life-Cycle Studies section of its bi-monthly magazine, World Watch. This print-exclusive content is now available for free to Eye on Earth readers. Look for a new study every Friday!

Overview

Corn was once a simple food, chewed off the cob. Now, with corn reinvented and transformed, it takes a chemist to recognize all its offspring. Among these is high-fructose corn syrup (a gooey sweetener used in soft drinks, meats, cheeses, and dozens more foods) that appeases confectionary cravings. But recent studies have raised concerns about the syrup by drawing links to obesity and other health effects.

High-fructose corn syrup (HFCS), also called isoglucose, is mainly a blend of two sugars, fructose and glucose. Soda and ice cream often blend 55 percent fructose and 45 percent glucose, while the HFCS used in canned fruits and condiments is generally a 42/48 percent mix (with other ingredients). White sugar is a 50/50 split.

In the United States, heavy corn subsidies and sugar-import barriers have made HFCS some 20 percent cheaper than sugar. The United States accounted for nearly 80 percent of global production in 2004 and U.S. consumers swallowed 58 pounds of the syrup per person last year in various products, according to the U.S. Department of Agriculture (USDA). Other producers include Japan, Argentina, the European Union, and China.

Production

U.S. refineries discovered in the 1860s that mixing liquefied cornstarch with either acids or enzymes rearranges sugar molecules into a dextrose solution (a form of glucose). Chemists mixed dextrose with additional enzymes in the 1940s for the first batches of HFCS. The syrup was not quite as sweet as sugar itself until 1971, when a Japanese chemist's further tweaking perfected HFCS, according to the Corn Refiners Association.

The food industry began to replace cane and beet sugar with HFCS after sugar prices quadrupled in the 1970s, and a few years later soft-drink companies followed suit. The syrup's affordability in the United States has helped soda companies sell larger bottles and greatly expand consumption of the calorie-rich drinks.

As HFCS spreads to parts of the developing world, dietary concerns are convincing many U.S. consumers to avoid it. In response, a growing number of sweetened products are being reformulated with cane sugar.

Corn farmPhoto courtesy USDA

The environmental impact of high-fructose corn syrup depends on how the corn is grown. " class="caption" align="" height="170" width="250">

Photo courtesy USDA

The environmental impact of high-fructose corn syrup depends on how the corn is grown.
Impact

Some claim that HFCS's global expansion and the parallel increase in obesity are linked. The concerned dietitians argue that, unlike glucose, which triggers appetite-suppressing signals in the body, fructose does not tell its eaters to stop. The theory remains unproven, but a growing body of literature has suggested the syrup may indeed counteract the satiation-hormone leptin. Conflicting research, supported by the American Beverage Institute, insists HFCS is no different than other sweeteners and is "safe in moderation."

The latest health concern stems from a recent Environmental Health study that found mercury in samples from two HFCS manufacturers. Chemicals mixed during production to stabilize pH may have contributed the toxic metal, the study said. The industry accuses the research of using "scant data of questionable quality."

The environmental impact of HFCS depends on how the corn is grown. Conventional farming practices use significant water resources, pesticides, and fertilizers, leading to widespread water pollution and nutrient-depleted soil. Corn production has also become a major contributor to climate change. In The Omnivore's Dilemma, author Michael Pollan estimates that between one-quarter and one-third gallons (about 1.0 to 1.25 liters) of oil are needed per bushel of corn to create the pesticides, fertilizers, and tractor gasoline, and to harvest, dry, and transport the corn. The U.S. high-fructose corn syrup industry used about 490 million bushels of corn last year, according to USDA.

Ben Block is the staff writer for World Watch. He can be reached at bblock@worldwatch.org.

For permission to republish this article, please contact Juli Diamond at jdiamond@worldwatch.org.

Thursday, April 15, 2010

Fw: FDA Food Tyranny: The Empire Strikes Back!

Fake "Food Safety" Bill S.510 Amended: Can we Trust the FDA? NOT!

http://www.healthfreedomusa.org/index.php?p=5144

Regulation Courtesy of Kafka

Harkin's S. 510 claims to protect supplements while FDA Creates a Wide-Open Back Door to Destroy Them While We Are Still Celebrating

Not long ago, a form of Vitamin B6 (pryadoxamine) was forbidden by the FDA because a drug company had studied it and wanted to make it into a drug.  Never mind that it was protected by the 1994 Dietary Supplements Health and Education Act (DSHEA) as a grandfathered item on the "Old Ingredients List".  Recently the Fraud and Death Administration said that although we know that it had been in use before DSHEA and WAS on the list found on the FDA website, being on the list was not (hold on to your hats here) proof of being on the list and thus not proof of being grandfathered. 

Now, because another drug company wants to make another form of Vitamin B6 into a drug, and it fears, in writing, that people would take the supplement rather than the drug if it were not banned as a supplement, The FDA is considering granting its Citizens Petition to do just that.

Next, walnuts.  Because Blue Diamond refers to studies showing that walnuts can be good for you, they have received a letter from the brutal and deeply corrupt FDA stating that giving out that informaton has turned their product, walnuts, into a drug and, as such, it can no longer be sold in the US.

Absurd?  Yes.  Unexpected? No.  This is precisely what we told you the FDA was up to with their insane and wildly dangerous Draft CAM Guidance of just over two years ago.  So here is the FDA, not able to promulgate this regulation because 688,000 of you wrote to the FDA saying that this criminalization of knowledge and natural health options was not acceptable to you. 

We told you that our victory was significant when they abandoned this guidance, but that they would be back to accomplish the same thing at a later date. 

Well, it's later now.

And your food AND your supplements are at tremendous risk. The Food and Death Administration is working hand in glove with Big Agribiz, which is really Big Pharma and Big Chema and Big Biotech all rolled into one, to degrade your food to those ghastly international standards known as Codex Alimentarius. 

As always, the Natural Solutions Foundation led the health freedom community in sounding the warning about the fake food and supplement "safety" bills pending before the Senate of the United States. Our supporters have heeded that warning and delivered well over one million messages to Congress demanding NO fake safety bills, while insisting that Congress provide protection for our supplements and natural remedies, not Codex HARMonization to destroy them, as has already happened in Canada and the EU.

Exactly as we predicted and feared, attempts were made to include the worst parts of Senator McCain's dreadful anti supplement S.3002 in a revised effort to get S.510 passed. We saw that one coming, although, once again, others who should have known better, told us we were crazy. Once again, we asked you to message Congress through the Natural Solutions Foundation Action Item. Many hundreds of thousands of emails later, language was inserted into Senator Harkin's gift to Big Agribiz (and, because of the disease this contaminated food will engender, Big Pharma as well) which amended S. 510 to "protect" DSHEA products (that is, to protect dietary supplements). That sounds good ….but it is the same hollow victory that the other health freedom folks trumpeted when S. 3002 was killed - they celebrated and tooted their own horns, but we told you that something was defintitely rotten with this deal. So it was.

Something is rotten with this deal, too. What's rotten is the FDA, which regularly chooses to act outside of, or even in direct opposition to, the law of the land.  Why will S. 510 be any different?  Would you buy a used car from this agency? AND let's not forget that S. 510 gives Big Argribiz total control of your food suppy.

So While It Would Be Nice to Claim That We Won This Round, It Is Not Completely True - YET!

We Got a Very Partial Stay of Supplement Exterminatin......But That's Not Nearly Good Enough.

Here's what IS good enough: We want natural remedies and holistic techniques (like Holistic Ear Candling, for example) and all natural, local, community, family and farm food production fully protected too… better yet, DEFEAT S.510!

Read more here: http://www.healthfreedomusa.org/?p=5144

And take the Action Item here:
http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=26714


Drug firm investigated FDA officials - Eamon Javers - POLITICO.com

Drug firm investigated FDA officials - Eamon Javers - POLITICO.com:


Drug firm investigated FDA officials
By: Eamon Javers
March 30, 2010 07:45 PM EDT

For more than two months in late 2008, private investigators working for a drug company gathered information on a high-ranking official at the Food and Drug Administration — unearthing details about her husband, two daughters and in-laws and retracing her steps on a business trip she took to Thailand.

The drug company, Amphastar Pharmaceuticals Inc., paid more than $100,000 to Kroll, the New York-based private investigative firm, to uncover the information about Janet Woodcock, director of the FDA’s Center for Drug Evaluation and Research, who oversees the agency’s new-drug approvals.

At stake for Amphastar, a generic drug maker, was whether the FDA would allow it to bring to market a version of a prescription drug for blood clots and gain access to a market worth more than $3 billion.

On behalf of the drug company, Kroll also investigated a second FDA official — Moheb Nasr, director of the FDA’s Office of New Drug Quality Assessment, creating a file on him that included his birth date, the price he paid for his home and details of his education and professional background.

Amphastar says the investigation was done in order to find out if Woodcock or Nasr was unfairly favoring a competitor in the drug approval process and that it did nothing wrong.

“I feel like, as a citizen, you have a right to question your government and a right to look at public information,” said Amphastar’s general counsel, Jason Shandell. “There was no impropriety here.”

Shandell said the investigation was limited to public records, database searches and other information available to the general public.

But the case has attracted the attention of investigators working for Senate Finance Committee Chairman Max Baucus (D-Mont.), who said it was “an outrage” and has demanded that Kroll tell him how often private detectives target public officials. He also had harsh words for Amphastar.

“Pharmaceutical companies should be focusing on getting their drugs approved based on health research and science rather than wasting their resources hiring private investigators to snoop around the lives of FDA regulators and their families,” he said.

The details of the drug company investigation, which came to light after committee investigators requested documents from Amphastar last fall, offer a rare glimpse inside the world of high-stakes corporate detective work.

At one point, the investigators hired a freelance reporter to file Freedom of Information Act requests, using her status as a journalist to request Woodcock’s e-mails, phone records, voice mails, calendars and expense reports, among other documents — without mentioning that she was being paid for her efforts by a private investigative firm.

“I am making this request as a journalist and this information is of timely value,” Melanie Haiken, a San Francisco-based freelance reporter, wrote to the FDA. “As a journalist, I am primarily engaged in disseminating information.”
Haiken did not disclose that she was working for the private investigators at the time. In an e-mail explaining its fees, Kroll told Amphastar that the expenses related to the FOIA covered “the cost of the person we are using to make the requests untraceable to you, the client.”

“I am wondering if this is an isolated instance or if Kroll is using journalists, who purport to be working in the public interest, to file FOIA requests on behalf of clients in order to take advantage of reduced fees and expedited processing,” Baucus wrote in a letter to Kroll CEO Ben Allen.

Woodcock and Nasr did not respond to requests for comment. Neither did the FDA.

Amphastar turned to Kroll in late 2008, after becoming increasingly frustrated that the FDA was dragging its feet in approving the company’s generic-drug application for low-molecular-weight heparin. In addition, the company’s executives became worried that the FDA was favoring a competitor, Massachusetts-based drug manufacturer Momenta Pharmaceuticals, and suspected that Woodcock, the official they blamed for the delays, was somehow allied with Momenta.

As evidence, Amphastar pointed to a paper Woodcock had co-authored with Momenta co-founder Ram Sasisekharan. And, it noted, Woodcock had been a featured speaker along with him at the Shangri-La Hotel in Bangkok in 2007.

Collusion between FDA officials and drug companies has happened before — a history Amphastar was well aware of when it launched its investigation.

In 1989, three FDA officials pleaded guilty to taking bribes and two companies said they had submitted false information to the government in a scandal that rocked the pharmaceutical world. And that scandal came to light only because an aggrieved drug company had hired private investigators to dig into suspicious relationships.

According to a document titled “Suggested Items for Investigation,” Kroll’s plan for investigating Amphastar included digging up information on “[Janet Woodcock] and her relatives and friends; J.W.’s financial status and lifestyle change since 2004; any entities ... that JW, her relatives or friends partially own or are affiliated with in the U.S.”

Other objectives included determining if Woodcock or any of her family members maintained any Swiss or Cayman Islands bank accounts or companies.

By the end of October 2008, Kroll had completed an “interim report” on Woodcock and Nasr. In it, Kroll detailed Woodcock’s birth date, the state in which her Social Security number had been issued, the identity of her husband, Roger Miller, their home address and the value of her Brookeville, Md., home. Kroll also uncovered similar details about Nasr.

But Kroll had come up empty — finding little evidence of an improper connection.

“To date, Kroll has identified no reports indicating that Woodcock’s relationships with Nasr [and another individual] are anything but of a professional nature,” Kroll concluded. “Kroll has identified no personal or business links with the Sasisekharan family other than Woodcock and Ram Sasisekharan’s well-publicized, jointly authored reports.”

But despite the report, Amphastar in April 2009 filed a complaint with the FDA, alleging that Woodcock and Momenta had an improper connection.

“Sure, we don’t have a smoking gun,” Shandell said, “but there appears to be some relationship between these two that goes beyond the typical FDA relationship.”

The FDA’s legal counsel, however, said in February that Woodcock’s interactions with Momenta did not constitute a conflict of interest.

Rick Shea, the chief financial officer for Momenta, also said his company acted properly in its interactions with the FDA. “There certainly was no inappropriate relationship between anybody at Momenta or anybody associated with Momenta and anybody at the FDA,” Shea said.

Haiken, the freelance journalist, confirms that she filed the FOIA on behalf of Kroll. But Haiken said her intent was journalistic and that she hoped the FOIAs would yield an interesting story. “I’m not really an investigator, I’m a health writer,” she said. “I have a right to get a story tip from somebody, even if it’s somebody at Kroll.”

Individual investigators inside Kroll billed for their time like lawyers, with rates ranging from $125 to $390 per hour. By the end of November, the company had charged Amphastar more than $100,000. Its invoice included $596.25 for “calls to Thailand regarding Woodcock’s hotel stay. Further research on … conference participants and board members. Further research on Woodcock schedule prior to and after the conference.”

Kroll also sent Amphastar a memo titled “Woodcock/Miller Family Members.” That document detailed the biography of Woodcock’s husband and information about the couple’s two daughters.

An outside public relations consultant for Kroll issued a statement in response to POLITICO’s questions about its investigation.

“We have received Senator Baucus’s letter and will review the request, bearing in mind our obligations to our client and client confidentiality,” Kroll said.



© 2010 Capitol News Company, LLC

Thursday, October 15, 2009

Officials Say Don't Blame the Swine Flu Shot, You'll Drop Dead Anyway | Farm Wars

Vaccines BHP copy

The H1N1 vaccination propaganda machine is going full-tilt, and the timetable for rapid population reduction is upon us. This is soooooo obvious, people! They are telling us what is going to happen before it happens, because they are going to cause it. They know people will drop dead after the shot, and are putting out the pre-op denial propaganda so that people will think, ‘hey, they warned us of this, and it is nothing to worry about.’

Don’t Blame Flu Shots for All Ills, Officials Say

As soon as swine flu vaccinations start next month, some people getting them will drop dead of heart attacks or strokes, some children will have seizures and some pregnant women will miscarry. But those events will not necessarily have anything to do with the vaccine. That poses a public relations challenge for federal officials, who remember how sensational reports of deaths and illnesses derailed the large-scale flu vaccine drive of 1976. This time they are making plans to respond rapidly to such events and to try to reassure a nervous public — and headline-hunting journalists — that the vaccine is not responsible. Every year, there are 1.1 million heart attacks in the United States, 795,000 strokes and 876,000 miscarriages, and 200,000 Americans have their first seizure. Inevitably, officials say, some of these will happen within hours or days of a flu shot…

And just to make sure that this vaccine is as lethal as possible, Washington suspends the law regarding the amount of mercury it can have.

Washington OKs mercury in swine flu vaccine

The state Health Department will allow more mercury than usual in some of the swine flu vaccine to make sure shots are available to pregnant women and children under age three.

The department says mercury-free swine flu vaccine may not always be in stock, so it wants to give people the choice of using vaccine with the mercury preservative called thimerosal, which is believed to be safe.

The Centers for Disease Control’s Web site says the following about thimerosal:

“There is no convincing scientific evidence of harm caused by the low doses of thimerosal in vaccines, except for minor reactions like redness and swelling at the injection site.

“However, in July 1999, the Public Health Service agencies, the American Academy of Pediatrics and vaccine manufacturers agreed that thimerosal should be reduced or eliminated in vaccines as a precautionary measure. Most vaccines for children under six are thimerosal-free.”

The suspension of the mercury limit announced Thursday lasts six months and applies only to the swine flu vaccine expected to become available in October…


Here is the priority list of recipients for swine flu shots once the vaccine arrives:

– Anyone age 6 months to 24 years

– Pregnant women

– Healthcare workers

– People under 50 with chronic illnesses

I guess they are keeping to the time-honored tradition of women and children first, and as an added bonus, their shots will most likely have added mercury, since the clinical trials for the vaccine on pregnant women is scheduled to end approximately 9 days before the vaccine goes on the market for that target group.

I remember when the adjuvant Thimerosal (mercury) came out for horse vaccines. Horses were having a very bad reaction to it, and most people that I know of knew this and avoided them. Well, I guess if it is bad for horses, it must be good for people.

Mass Vaccination Schedule

The H1N1 vaccine was approved on September 15, 2009, with clinical trials done in mid-August for most adults. Vaccine clinical trials for pregnant women started on September 17, 2009, and a full-scale vaccination effort for all groups of people is set to begin in mid-October.

The FDA reported the following on September 15, 2009 regarding vaccine approval for most adults:

FDA Approves Vaccines for 2009 H1N1 Influenza Virus

The H1N1 vaccines approved today undergo the same rigorous FDA manufacturing oversight, product quality testing and lot release procedures that apply to seasonal influenza vaccines.

Testing began shortly thereafter for children, and the following was reported by ABC on September 17, 2009 regarding clinical trials for pregnant women:

Twenty participants in the trial will get two doses 21 days apart and they’ll be monitored in several different ways. Their cord blood will be checked too to see how it’s affecting the unborn child.

On September 15, 2009, Reuters reported:

U.S. officials are launching a large-scale vaccination effort in mid-October to inoculate the population, including those most at risk such as pregnant women and young people ages 6 months to 24 years.

Let’s take a closer look at the clinical testing procedure. They start testing on pregnant women on September 15. The women get 2 doses, 21 days apart, and are tested. That would mean that on September 15, they would get the first dose, and 21 days later, Oct. 6, the second. The vaccination program is scheduled to start mid-Oct., which is around Oct. 15. That leaves approximately 9 days to determine that the vaccine is safe, and get it ready for distribution.

Running a pretty tight schedule there, eh? Jab ‘em and if they don’t drop dead in 21 days, jab ‘em again. If they don’t collapse on the second jab, then it’s on to the public we go! So much for extensive testing. Wait, didn’t I just read something about rigorous FDA testing?

“The H1N1 vaccines approved today undergo the same rigorous FDA manufacturing oversight, product quality testing and lot release procedures that apply to seasonal influenza vaccines,” Dr. Jesse Goodman, FDA’s acting chief scientist, said in a statement.

Just how rigorous can that testing be if between the last shot and full scale implementation on the population is a mere 9 days? Has anyone tried to get tests back from the lab lately? How long did it take? This is a done deal, folks. They don’t care if people drop dead because the PR spin is already in high gear. In fact, they are boldly telling us what is going to happen before it happens, because they are going to cause it. They know people will drop dead or get sick after the shot, and are putting out the pre-op denial propaganda so that people will think, ‘hey, they warned us of this, and it is nothing to worry about – it couldn’t possibly be the vaccine, they said so.’

Let me tell you, if I look at someone and that person receives a vaccination, and then drops dead 5 minutes later, IT WAS THE VACCINE! No amount of denial will convince me otherwise. This is a eugenics program, plain and simple. And as any good eugenics program goes, it is being forced on the public by any means possible.

Implementing the Mass Vaccination Program

Let’s look at how this vaccination program is being implemented. After all, it is supposed to be voluntary, right? After all, Obama said so. NOT! Here are the steps:

1. First they try and get you to comply through a propaganda campaign to effect voluntary compliance.

2. Second, they try and get you to take it under color of law.

3. Third, it becomes mandatory

The Propaganda Campaign

Any good vaccination propaganda campaign will start with the demonization of target groups to effect voluntary compliance. Propaganda is used to convince the public that the unvaccinated pose a threat to what is called “herd immunity.” Herd immunity is defined by the Free Medical Dictionary as:

The resistance of a group to attack by a disease to which a large proportion of the members are immune.

If you take the vaccine, you are supposed to be immune, correct? If you don’t take the vaccine, you are supposed to be susceptible to the virus. Why should the vaccinated worry about the unvaccinated if they are immune? If people do not want to take the vaccine and decide to protect themselves via natural methods, how does that affect supposed “herd immunity?” Are we a bunch of cattle that lose value if we get sick? The H1N1 is not a major health risk. The regular seasonal flu is worse than the H1N1 variety, and even health professionals refuse to take it. Yet, the propaganda goes on to convince people that if certain groups of people do not take the vaccine, then “herd immunity” is compromised, and everyone is in danger. Take this piece from the Yale Journal of Biology and Medicine:

Mandatory School Vaccinations: The Role of Tort Law

“Religious Communities as Disease “Hot Spots.”

Governments traditionally have considered “communities” in relatively broad terms, viewing entire states — or sometimes even the whole nation — as a “community” for herd immunity purposes [14]. However, recent experiences have demonstrated that actual communities are far smaller. For instance, although nationwide measles vaccination rates appeared high enough to ensure national herd immunity, disproportionately low vaccination rates among blacks and Hispanics resulted in measles outbreaks in several large urban areas, most notably Los Angeles [15].

Religious communities — particularly Christian Science, Amish, and Mennonite communities — have been the source of many preventable disease outbreaks in recent years. Diseases from polio [16] to measles [17] to rubella [18] have resurfaced with increasing frequency in the United States due to herd immunity being lost in such religious ghettos. This comes at a tremendous cost to society, for “vaccine-preventable diseases impose $10 billion worth of healthcare costs and over 30,000 otherwise avoidable deaths in America each year” [19].”

Religious ghettos? A typical propaganda technique and scare tactic – demonize the opposition, then accuse it of infecting others and lay blame. If people get sick because they do not take the vaccine, then your health care costs will go up. But wait, it gets better:

For decades, all 50 states have required that parents vaccinate their children against various diseases, including polio and measles, as a prerequisite to enrolling them in public schools [1]. While virtually all states have tailored their immunization statutes to exempt those with religious (and sometimes philosophical) objections to vaccines from these requirements [2], widespread use of these exemptions threatens to undermine many of the benefits of mandatory vaccinations, such as preserving “herd immunity” [3]. Since it is unlikely that state governments will eliminate such exemptions outright, society must consider other methods of providing incentives for vaccination and compensating those who have suffered due to a disease outbreak caused by a community’s loss of herd immunity.

Now the vaccinated become the victims of the unvaccinated because they may have suffered due to a disease outbreak caused by a lack of “herd immunity,” and the unvaccinated can be threatened with a Tort lawsuit for “failure to vaccinate” if someone gets a disease and an unvaccinated person happens to be there.

The following article from Dr. Sherri Tenpenny shows how the Amish were used to advance “herd immunity” propaganda:

On October 14, [2005] the major media outlets shrieked a report of “the first outbreak of polio in the United States in 26 years,” occurring in an Amish community in central Minnesota. The specter of hundreds of children in braces and iron lung machines lining the halls of hospitals immediately danced through the air, and directly into the minds of parents who have chosen to not vaccinate their children.

“First of all, there wasn’t an “outbreak of polio.” There was only the discovery of an inactivated polio virus in the stool of four children. The first confirmation was in a 7-month old Amish infant, presumably hospitalized, with severe immune deficiency. The “find” prompted screening of other children in the community; four children were confirmed positive. None experienced any type of paralysis.

Part of the panic can be blamed on inaccurate reporting. The virus that was identified was not “wild polio.” It was a virus that is found only in the oral polio vaccine (OPV). Oral vaccine-strain viruses are inactivated with formaldehyde and are generally considered by the CDC “too weak” to cause disease. Even though the OPV is still used extensively in Third World countries, it has not been used in the United States since 2000. How did children in an isolated Amish community, with no exposure to foreigners, become exposed to vaccine-strain polio virus? That remains a mystery.

Color of Law

Now let’s take a look at what is known as the color of law. It is not against the law to not vaccinate your children. However, non-mandatory vaccinations do not have to be law to be mandatory. If the system around you forces you to do something against your will or suffer penalties for non-compliance via the back door approach such as the following example, then the result is the same as if there was a mandatory vaccination law.

Example: If your kids are enrolled in a public school, and you cannot homeschool them because of economics or other hardship, then you face mandatory vaccines. If you go the waiver route, then public officials can make it extremely difficult if not impossible to comply with the waiver requirements, and you end up violating an actual law requiring enrollment of your child in school. You’ve got to get them to school on time or face penalties for compulsory education violations because you refused the vaccinations and did not complete the waiver in time for the start of school. This is how non-mandatory becomes mandatory without being law, but is enforced under color of law.

Note: color of law. The appearance or semblance, without the substance, of a legal right. • The term usu. implies a misuse of power made possible because the wrongdoer is clothed with the authority of the state. State action is synonymous with color of [state] law in the context of federal civil-rights statutes or criminal law. See STATE ACTION. [Cases: Civil Rights key1323. C.J.S. Civil Rights §§ 92-94.] BLACK’S LAW DICTIONARY 282 (8th ed. 2004)

Mandatory Programs

When outright propaganda and color of law don’t work, and not enough people take the vaccine, it becomes mandatory. All semblance of fair play is now thrown out, and the real motive becomes clear. Take the vaccine or else.

N.Y. Health Care Workers Revolt Over H1N1 Vaccine

They’re upset over an ultimatum from the health department. Workers are being told to either get the swine flu vaccine or lose their jobs.

New York is the first state in the country to mandate flu vaccinations for its health care workers. The first doses of swine flu vaccine will be available beginning next week. Much of it is reserved for state health care workers, but there is growing opposition to required inoculations.

Health care workers in Hauppauge screamed “No forced shots!” as they rallied Tuesday against the state regulation requiring them to roll up their sleeves.

“I don’t even tend to the sick. I am in the nutrition field. They are telling me I must get the shot because I work in a health clinic setting,” said Paula Small, a Women, Infants and Children health care worker.

Small said she will refuse, worried the vaccine is untested and unproven, leaving her vulnerable. In 1976, there were some deaths associated with a swine flu vaccination.

Registered nurse Frank Mannino, 50, was also angry. He said the state regulation violates his personal freedom and civil rights. “And now I will lose my job if I don’t take the regular flu shot or the swine flu shot.”

When asked if he’s willing to lose his job, Mannino said, “Absolutely. I will not take it, will not be forced. This is still America.”

The protest also shook Albany Tuesday. Hundreds of demonstrators demanded freedom of choice. After all, as health care professionals they argue they’re already constantly washing their hands and aren’t likely to transmit or contract the flu.

Around 500,000 health care workers are slated to receive the vaccine.

“It’s certainly their prerogative to voice their opinion,” said Dr. Susan Donelan of Stony Brook University Hospital. Donelan said most in the medical community see the benefits and safety of the shots and welcome them, and that hospitals must obey the law. “Our hospital is committed to following the mandate to have our personnel vaccinated,” she said.

The state said change was needed this year to save lives, typically only about 45 percent of health care workers take advantage of voluntary flu vaccines.

More than 150 institutional outbreaks of seasonal and H1N1 flu are expected this year in hospitals, nursing homes and hospice centers. New York and New Jersey will get their first doses of the swine flu vaccine next week. It will be the nasal mist, not a shot.

Dangers of Recombination

Now that we have looked at the supposed “rigorous testing procedures,” the potentially harmful doses of mercury involved, and how a mandatory vaccination program is implemented, let’s take a look at another danger that the vaccination program pushers don’t want you to know about.

Jeffrey M. Smith shows us the dangers of genetically modified live virus vaccines, such as the H1N1:

GM Vaccines Recombine into Unpredictable Hybrid

In what may be the first experiment of its kind, scientists infected cell cultures with two related viruses. One was a genetically engineered poxvirus, (vaccinia virus (VIC) with a transgene from the influenza virus). The other was a naturally occurring relative of the first virus, isolated from Norwegian wildlife. Both were orthopoxviruses. The two viruses interacted and created many new hybrid viruses by recombination. The characteristics of some of the new viruses included traits not expressed in either parent virus. Some viruses, for example, spread faster than either parent, while others produced different, more serious cell culture changes. A single virus multiplied into hundreds of thousands of viruses in a few hours, with unpredictable consequences. Since the marker gene in the transgenic virus was not present in some of the newly formed hybrid viruses, it would not be possible to track transgenic viruses as the origin of the hybrids, if they were found in the wild.

When a person receives a dose of the genetically engineered H1N1 live virus vaccine, that virus has the potential to recombine in the host. As with all live virus vaccines, the host will shed this newly recombined virus for around 21 days after inoculation. Persons who come in contact with the newly inoculated are subjected not to the original virus, but the newly recombined one thanks to genetic engineering. The new virus is potentially more lethal than the original live vaccine virus. This is the way to spread a lethal strain of flu to whatever segment of the population you are aiming to destroy. Create a virus via genetic engineering, inject as many as you can with it, and let nature do the rest.

The powers that be do not want anyone to know about the active shedding threat because they want the genetically modified recombined virus to spread just as far and wide as possible, thereby validating their fear mongering and creating more of a demand for the product (vaccine). This validation justifies all of the emergency measures already in place, such as quarantine facilities, forced vaccination checkpoints, etc.

It is a typical marketing ploy used in a most evil way.

Summation

We have a vaccine that has undergone such a limited “testing” that no sane person would willingly take it, the law regarding the amount of mercury allowed in vaccines has been suspended just so this one can have a bigger dose of it, and they are targeting pregnant women and children first.

The vaccine is supposedly voluntary, yet certain segments of the population are required to have it to keep their jobs. The health department has made mandatory the vaccines for health care workers already, and if not enough people take it to meet the “herd immunity” quota, it becomes mandatory for everyone. A certain percentage of the population has to take the shot to be active carriers in order to shed the virus to others to reduce the population to 500 mil, as required by eugenicists.

A Possible Scenario

I anticipate that we will have a window of opportunity that will last while the H1N1 flu shot volunteers run to the pharmas for their shot when they become available on or around October 15. There is a formula that is used to determine what percentage of the populace needs to be vaccinated to maintain “herd immunity,” and the time schedule for forced vaccinations will be based on that, at least for a little while.

“Herd immunity” propaganda statistics will be used to implement forced vaccinations. If not enough people volunteer for the shots, “herd immunity” is supposedly compromised and a national health emergency can be declared, and people will buy into it.

When the live genetically modified virus recombines in the host and the vaccinated shed the newly mutated virus, people will be getting sick from having contact with the vaccinated, and this will reinforce the need for forced vaccinations to “solve the problem.” More people will rush to get the vaccine “cure” and more live genetically modified virus will be passed on to others.

This will snowball into an all-out emergency event, which will involve the use of checkpoints, FEMA camps for quarantine, and martial law. We want to be off the streets as much as possible to avoid not only any quarantine and mandatory shot procedures, but also the mutated virus.

I hope I am wrong, but I am advising everyone reading this to be prepared just in case I am right.

©2009, Barbara H. Peterson

NOTES:

herd immunity:

The Mathematics of Mass Vaccination

http://en.wikipedia.org/wiki/Mathematical_modelling_of_infectious_disease#The_mathematics_of_mass_vaccination

Friday, July 31, 2009

WHO | Strategic Advisory Group of Experts (SAGE) on Immunization

Strategic Advisory Group of Experts (SAGE) on Immunization

The Strategic Advisory Group of Experts (SAGE) on Immunization was established by the Director-General of the World Health Organization in 1999 to provide guidance on the work of the WHO Immunization Department. The Terms of referenceof the Group were revised during 2007 in view of the development of the Global Immunization Vision and Strategy (GIVS). SAGE is the principal advisory group to WHO for vaccines and immunization. It is charged with advising WHO on overall global policies and strategies, ranging from vaccine and technology, research and development, to delivery of immunization and its linkages with other health interventions. SAGE is concerned not just with childhood vaccines and immunization, but all vaccine-preventable diseases.

SAGE Members

It is Official: WHO Recommends Mandatory Injections to Almost Two Hundred Countries « Speak Truth 2 Power

It is Official: WHO Recommends Mandatory Injections to Almost Two Hundred Countries

vaccinations1by Barbara Minton, Natural Health Editor
Naturalnews.com

Executives from Baxter, Novartis, Glaxo-Smith Kline, and Sanofi Pasteur have seats at the advisory group that on July 13th recommended mandatory H1N1 vaccination of everyone in all 194 countries that belong to the World Health Organization (WHO), according to a report just issued by journalist Jane Burgermeister. WHO spokesperson Alphaluck Bhatiasevi confirmed that Dr. Margaret Chan did not give the press briefing at WHO headquarters in Geneva as anticipated. At short notice, Dr. Marie-Paule Kieny stepped in to announce that “vaccines will be needed in all countries.”

According to WHO documents, vaccines “such as those that are formulated with oil-in-water adjuvants and live attenuated influenza vaccines are important.” Health workers, pregnant women, healthy young adults of 15 to 49 years, and healthy children will be the targeted groups of the world wide vaccine effort.

“All countries should immunize their health-care workers as a first priority to protect the essential health infrastructure. As vaccines available initially will not be sufficient, a step-wise approach to vaccinate particular groups may be considered,” according to Paule-Kieny. The Strategic Advisory Group of Experts (SAGE) on Immunisation established by the Director-General of the WHO in 1999, suggested the following groups for consideration, noting that countries need to determine their order of priority based on country-specific conditions: pregnant women; children over the age of 6 months with one of several chronic medical conditions; healthy young adults of 15 to 49 years of age; healthy children; healthy adults of 50 to 64 years of age; and healthy adults of 65 years of age and above.

Wednesday, July 08, 2009

Pandemic Flu for Depopulation

Video: Jane Burgermeister interview on Swine Flu Depopulation « Dprogram.net:

I have made contact with Jane Burgermeister and she sent me the files. I have created a scribd account:

http://www.scribd.com/91177info

Actual files for viewing and downloading:

Evidence of the Use of Pandemic Flu to Depopulate USA

http://www.scribd.com/full/17044769?a…

Criminal Charges – Swine Flu Edits v2[1]

http://www.scribd.com/full/17044758?a…

These are the ones that have not been hacked/changed etc.

The Michael Jackson connection is total disinfo to turn it into a conspiracy.

I will be adding documents to this scribd account as I get them.

MORE INFO TO COME IN A HURRY

Original radio interview is here: http://www.blogtalkradio.com/Drew-Mal…

Part 1 of 4

Part 2 of 4

Part 3 of 4

Part 4 of 4