osterhaus' corporatistische staatsmanipulatie in beeld en geluid

Deel presentatie Osterhaus: hier leren we welke bedrijven berokken zijn bij het staatsonderzoek. Zelf haalt Osterhaus de WHO nog aan.


Hier leren we dat de hulpstoffen separaat worden ingekocht en opgeslagen. Osterhaus stelt dat dit het duurste bestanddeel is van de vaccins. Voorts stelt hij dat de houdbaarheid veel langer is dan die van het antibodies.

Debat/college - Eckelenkamp en Osterhaus.

Instructief is de manipulatieve manier van communiceren van Osterhaus.

Draaien, overspoelen met gegevens, name calling en marginalisering van de ander zijn de belangrijkste pijlers onder zijn verhaal.

Wel even een kleine twee uur voor uittrekken.

Note: Ook Eckelenkamp adept van de allopathie en is voorstander van vaccineren

Note2 Over squaleen gaat het niet. Alles wordt ontleed, behalve de adjuvants

meer over squaleen

The US government has contracted with at least 5 pharmaceutical manufacturers to develop and produce H1N1 vaccines, using a variety of platforms and manufacturing methods...

A novel feature of the two H1N1 vaccines being developed by companies Novartis and Glaxo-Smith Kline is the addition of squalene-containing adjuvants to boost immunogenicity and dramatically reduce the amount of viral antigen needed. This translates to much faster production of desired vaccine quantities.

Each company has its own proprietary adjuvant, acquired in each case at high cost and intended for the high-stakes business of rapidly producing vaccines for novel pandemics or biological warfare threats.

Novartis' adjuvant is named MF59, and Glaxo's is ASO3. We know they work beautifully to strengthen vaccine efficacy. But how safe are they?

That is a very difficult question to answer. Novartis claims MF-59 has been used safely by over 40 million people. However, FDA has not seen fit to approve even a single US vaccine that contains these novel adjuvants.

art. dr Meryl Nass pub. Nass

Novartis mag toch voor 700 mio aan materiaal leveren

Novartis kreeg begin juli een order van het HHS voor de levering van MF59, of squaleen, ter waarde van $343.810.470. Antigen mogen ze leveren voor een waarde van:$346.334.450.

GlaxoSmithKline ontving voor haar hulpstof ASO3 een order ter waarde van $71.400.000.

Het antigen is het eigenlijke vaccin die het lichaam aan moet zetten tot de aanmaak van antilichamen. de squaleen is de "aanjager" . Volgens Novartis kan men door de MF59 volstaan met een kleinere hoeveelheid antigen om resultaat te bereiken.

Volgens Jane Burgermeister zijn deze middelen door US en EU regulators "classified as bioweapons".

Gevaarlijk zijn ze zeker.

novartis test vaccins met EN zonder hulpstof (squaleen)

foto: herr joerg reinhardt, COO novartis, voorheen verantwoordelijk voor vaccins en diagnostics

Onder een random testpopulatie van 6000 in Duitsland, UK en de VS. Ondertussen gaat de productie gewoon door.

Novartis is betrokken bij een Poolse Vogelgriep vaccin test in 2008. Daar zijn minstens 21 mensen aan gestorven. Dit vaccin tegen H5N1 is goedgekeurd door de EU.

In de VS worden squaleen en mercury als hulpstof slechts toegestaan bij noodsituaties. Een "uitbraak" van "Swine Flu" wordt beschouwd als noodsituatie.

De combinatie squaleen (Novartis en Baxter) in het eerste vaccin en levend virus in het tweede wordt door honderden medici beschouwd als zeer gevaarlijk.

Sanofi Pasteur is ook aan het testen EN produceren.

GlaxoSmithKline test NIET maar heeft wel een orderportefeulle van 291 mio vaccins.

GSK doet een "kleine test" met een van hulpstof voorzien vaccin (ik vermoed squaleen, maar krijg dit niet bevestigd) EN levert uit in Canada.

AstraZeneca test een vaccin dat via de neus wordt toegediend. Dit is een totaal ander verhaal, en voor Nederland niet relevant.

de noodzakelijkheid van squaleen geduid

Herb Newborg

YourSpine

August 5, 2009The U. S. government has paid pharmaceutical companies $7.9 billion* since 2004 to develop the capacity to mass vaccine the entire U.S. population by 2011. Under the perceived threat of H1N1, these plans have been accelerated to include the use of a non FDA approved chemical adjuvant suspected of causing Gulf War Syndrome, circumventing the FDA approval process for this potentially life threatening chemical.

In 2005, the Department of Health and Human Services (HHS) published a plan with two specific goals that relate to vaccines. The first goal was to have in place by 2011 domestic production capacity sufficient to supply vaccine to the entire U.S. population within six months of the onset of a pandemic. The second goal was to stockpile enough doses of vaccine to inoculate 20 million people as soon as possible after the onset of a pandemic.

As of September 15, 2008, HHS had yet to determine how best to build and develop the capacity to create the hundreds of millions of doses necessary for such an ambitious undertaking. Three options were identified which could possibly achieve the stated goal by 2011:

Continue to fund and expand funding for the egg-based vaccine antigen production currently utilized in the production of seasonal flu vaccine (viruses are grown in hens’ eggs). Toward this end, HHS has budgeted $600 million to offer capital subsidies to manufacturers to build egg-based production facilities in addition to $176 million already awarded.

Continue to fund and expand funding for cell-based vaccine antigen production (for example, viruses grown in the kidneys of dogs) widely used to manufacture vaccine against polio, chicken pox, measles, mumps, and rubella. To date, HHS has obligated $1.3 billion to promote the development of new cell-based influenza vaccines.

Fund next generation vaccine manufacturing, based on the use of recombinant-DNA technology. Recombinant vaccines are made by splicing antigen producing genes into the DNA of another organism (pigs, monkeys, birds, insects, etc.) The modified organisms then reproduce to provide bulk quantities of antigen. Recombinant techniques are already in use to make vaccines against hepatitis B and human papillomavirus.

All three scenarios had major drawbacks.

Using egg-based vaccine antigen to provide the quantities necessary to vaccinate all 300 million Americans with 2 doses each would require massive infrastructure build up. Despite the $176 million already awarded to manufactures, additional funds would be needed and FDA approvals (not expected until 2011) are necessary in order to even begin to approach the desired number of vaccine doses. It is estimated that the two companies awarded egg-based funding combined could produce only 125 million doses, even after the infrastructure upgrades, and not until 2011.

Using cell-based antigen to provide the quantities necessary to vaccinate all 300 million Americans with 2 doses each would also require massive infrastructure build up. A plant could produce 25 million pandemic-influenza doses at 90 micrograms per dose. It would take about nineteen plants with that capacity to produce 475 million doses. If the cost of construction, bringing the plant online, and obtaining the FDA’s approval averaged $400 million per plant, the total cost of the expanded capacity would be $7.6 billion. If each plant cost $600 million, the total would be $11.4 billion. This capacity would not be available until 2011-2012.

Next generation or recombinant-DNA is not an attractive option, as most recombinant influenza vaccines have not yet advanced past early-stage clinical trials. These vaccines could be 10 years or more away from the market. HHS has yet to fund their development for use against influenza, in part because it has chosen to build on the decades of experience in using cell culture to produce other vaccines. However, HHS plans to award contracts worth $155 million for the development of next-generation vaccines in the near future.

So where does the capacity to mass vaccinate the entire population stand after our $7.9 billion investment?

We currently have a stockpile of 22.5 million doses of the H5N1 antigen for the feared Avian flu pandemic that never materialized. The cost to maintain this stockpile for just two circulating strains of H5N1 is about $2.2 billion annually. Influenza vaccine typically expires after two years; 15 million doses have expired or will expire soon.

In addition, we have stockpiled 268 million doses of what appears to be the wildcard in the whole equation. This is what is known as an adjuvant. An adjuvant is a chemical that can be added to vaccines to reduce the amount of active ingredient (antigen) needed per dose of vaccine by “turbo-charging” the immune system response in the recipient. This could potentially stretch the supply, providing six times as many doses from the same quantity of antigen.

This would solve many, if not all of the issues regarding capacity to mass vaccinate the entire population. Instead of investing in building additional plants and hiring workers to produce antigen, the funds could be used to purchase proprietary, patented chemical adjuvants.

The only problem is: these chemicals are not FDA approved. They have not been FDA safety tested. We have no idea if they are safe and in fact have every reason to suspect that they are not.

Despite this fact, the U.S. has already purchased at least 312 million doses of two proprietary, patented adjuvants: MF59 from Novartis and ASO3 from GSK. These purchases took place despite the fact that neither chemical has been FDA approved for use in a vaccine. The manufacturers have not yet even obtained FDA approval for Phase I clinical trials in the U.S., the first step toward approval of any new drug, vaccine or adjuvant.

On average, it takes a little over a decade for a drug to move from preclinical development to the marketplace. Before a vaccine enters human testing, the developer conducts laboratory (in vitro) and laboratory animal (in vivo) testing to determine whether the product will be safe enough for researchers to proceed to clinical trials.

The developer must obtain the FDA’s approval to begin clinical trials through the submission of an investigational new drug, or IND, application. Clinical trials typically have three phases. Phase I focuses on the vaccine’s safety and generally involves fewer than 100 human subjects. The purpose of Phase II, which typically involves several hundred subjects, is to expand Phase I safety data and identify whether and at what dose the vaccine elicits a protective immune response. Phase III typically involves thousands of people and is used to document effectiveness and develop additional safety data (notably concerning the incidence and severity of side effects) required for licensing. Clinical trials generally last five to seven years. If all three phases of the clinical development are successful, the developer may submit a biologics license application, or BLA, to the FDA for review. If the FDA approves the application, the developer launches the new vaccine, a process that includes training its sales force and increasing production capabilities to meet the anticipated demand.

It appears that the U.S. is prepared to skip all of the normally required safety and efficacy procedures and allow for the massive testing of this novel adjuvant on at least 25% of the 12,000 Americans serving as paid clinical trial participants in tests of the new H1N1 vaccine, despite documented U.S. government warnings that adjuvanted vaccines can induce more pronounced side effects than ordinary vaccines, a definite downside because vaccines, unlike most other pharmaceuticals, are given to healthy people.

To date, the Food and Drug Administration has never approved an adjuvanted vaccine for influenza. Other adjuvanted vaccines currently licensed for use in the United States—against diphtheria, tetanus, hepatitis A, and hepatitis B—are made with aluminum. But aluminum adjuvants do not reduce the amount of antigen needed by enough to substantially increase the amount of vaccine that would be available during a pandemic.

The FDA has not approved a human vaccine containing a new type of adjuvant in many years, as all other types of adjuvants have thus far produced too many side effects to meet the FDA’s standards.

The reason introducing this chemical without the required safety and efficacy testing is so objectionable is that both of these proprietary adjuvants contain squalene.

Oil-based vaccination adjuvants like squalene have been proved to generate concentrated, unremitting immune responses over long periods of time according to a 2000 article in The American Journal of Pathology.

A 2000 study published in the American Journal of Pathology demonstrated a single injection of the adjuvant squalene into rats triggered “chronic, immune-mediated joint-specific inflammation,” also known as rheumatoid arthritis. The researchers concluded the study raised questions about the role of adjuvants in chronic inflammatory diseases.

What happens when Squalene is injected into humans?

Your immune system recognizes squalene as an oil molecule native to your body. It is found throughout your nervous system and brain. In fact, you can consume squalene in olive oil and not only will your immune system recognize it, you will also reap the benefits of its antioxidant properties.

The difference between “good” and “bad” squalene is the route by which it enters your body. Injection is an abnormal route of entry which incites your immune system to attack all the squalene in your body, not just the vaccine adjuvant.

Your immune system will attempt to destroy the molecule wherever it finds it, including in places where it occurs naturally, and where it is vital to the health of your nervous system, according to award-winning investigative journalist Gary Matsumoto, who explains there is a “close match between the squalene-induced diseases in animals and those observed in humans injected with this oil: rheumatoid arthritis, multiple sclerosis and systemic lupus erythematosus.”

“There are now data in more than two dozen peer-reviewed scientific papers, from ten different laboratories in the US, Europe, Asia and Australia, documenting that squalene-based adjuvants can induce autoimmune diseases in animals…observed in mice, rats, guinea pigs and rabbits. Sweden’s Karolinska Institute has demonstrated that squalene alone can induce the animal version of rheumatoid arthritis. The Polish Academy of Sciences has shown that in animals, squalene alone can produce catastrophic injury to the nervous system and the brain. The University of Florida Medical School has shown that in animals, squalene alone can induce production of antibodies specifically associated with systemic lupus erythematosus,” writes Matsumoto.

We got our first hint at the dangers of these proprietary adjuvants when they were secretly tested on soldiers during the Gulf War.

Gulf War veterans with Gulf War Syndrome (GWS) received anthrax vaccines which contained squalene. MF59 (the Novartis squalene adjuvant) was an unapproved ingredient in experimental anthrax vaccines and has since been linked to the devastating autoimmune diseases suffered by countless Gulf War vets according to data published in the February 2000 and August 2002 issues of Experimental and Molecular Pathology.

The Department of Defense made every attempt to deny that squalene was indeed an added contaminant in the anthrax vaccine administered to Persian Gulf war military personnel – deployed and non-deployed – as well as participants in the more recent Anthrax Vaccine Immunization Program (AVIP).

However, the FDA discovered the presence of squalene in certain lots of AVIP product. A test was developed to detect anti-squalene antibodies in GWS patients, and a clear link was established between the contaminated product and all the GWS sufferers who had been injected with the vaccine containing squalene.

The Pentagon never told Congress about the more than 20,000 hospitalizations involving troops who took the anthrax vaccine from 1998 through 2000, despite repeated promises that such cases would be publicly disclosed. Instead, generals and Defense Department officials claimed that fewer than 100 people were hospitalized or became seriously ill after receiving the shot, according to an investigation by the Daily Press of Newport News.

A study conducted at Tulane Medical School and published in the February 2000 issue of Experimental Molecular Pathology included these stunning statistics:

“ … the substantial majority (95%) of overtly ill deployed GWS patients had antibodies to squalene. All (100%) GWS patients immunized for service in Desert Shield/Desert Storm who did not deploy, but had the same signs and symptoms as those who did deploy, had antibodies to squalene.

In contrast, none (0%) of the deployed Persian Gulf veterans not showing signs and symptoms of GWS have antibodies to squalene. Neither patients with idiopathic autoimmune disease nor healthy controls had detectable serum antibodies to squalene. The majority of symptomatic GWS patients had serum antibodies to squalene.”

According to Dr. Viera Scheibner, Ph.D., a former principle research scientist for the government of Australia:

“… this adjuvant [squalene] contributed to the cascade of reactions called “Gulf War Syndrome,” documented in the soldiers involved in the Gulf War.

The symptoms they developed included arthritis, fibromyalgia, lymphadenopathy, rashes, photosensitive rashes, malar rashes, chronic fatigue, chronic headaches, abnormal body hair loss, non-healing skin lesions, aphthous ulcers, dizziness, weakness, memory loss, seizures, mood changes, neuropsychiatric problems, anti-thyroid effects, anaemia, elevated ESR (erythrocyte sedimentation rate), systemic lupus erythematosus, multiple sclerosis, ALS (amyotrophic lateral sclerosis), Raynaud’s phenomenon, Sjorgren’s syndrome, chronic diarrhoea, night sweats and low-grade fevers.”

Clearly bypassing the FDA requirements for safety testing of these new adjuvants and the vaccines which contain them puts the entire population at risk for serious, possibly life threatening side effects, particularly any of the 12,000 trial paid trial participants (6,000 children) who are unfortunate enough to be randomized into the adjuvant containing groups.

Still, on July 23, 2009, the FDA announced, “Currently, no U.S. licensed vaccine contains the adjuvants MF-59 or ASO3. It is expected that a novel influenza A (H1N1) vaccine manufactured using the same process as U.S. licensed seasonal inactivated influenza vaccine but administered with MF-59 or ASO3 will be authorized for emergency use only.”

And that, “Two of the manufacturers (Novartis and GSK) have proprietary oil-in-water adjuvants (MF-59 and ASO3, respectively) which have been evaluated in a number of clinical studies including studies with influenza vaccines. These manufacturers will include an evaluation of the utility of the adjuvant for dose sparing and enhanced immunogenicity in their clinical studies. While there may be exceptions, in general, studies which include an adjuvanted arm(s) to evaluate dose sparing and enhanced immunogenicity may be conducted concurrently in the adult and pediatric age groups in order to have timely immunogenicity results to guide pediatric dose recommendations.”

The same document indicates that vaccines containing the un-approved adjuvants will be given to 100 children 6 months to 3 years old, 100 children 3 years old to 8 years, 100 individuals 18 to 64 years old and 100 individuals 65 and older in each of the multiple clinical trials. In addition, 700 individuals in each trial will be given non-adjuvanted vaccine.

Since the government has recruited 12,000 paid “volunteers” for the trials, it would be possible that as many as 10 trials could be conducted simultaneously.

Oddly, 60% of the world’s confirmed cases have occurred in people age 18 or younger, yet this age group (between 8 and 18) have been excluded from the clinical trials, with the results for this age group to be extrapolated from the other study data.

Given the fact the U.S. currently owns 268 million doses of the non-approved, non FDA tested adjuvant, the vaccines that contain this novel chemical will likely be found to be completely safe in these industry run trials. Unfortunately, the effects on the soldiers that experienced injury sometimes appeared long after the planned duration of the current trials.

*$5.6 billion in funding occurred in 2006 alone. The $5.6 billion spent for vaccine development in 2006 is 100 times the $515 million the FDA spent in 2006 for all FDA activity related to drug safety and efficacy for the entire drug industry including: pre and post approval testing, approval and regulation of over-the-counter and prescription drugs, biological therapeutics and generic drugs and personal care products such as fluoride toothpaste, antiperspirants, dandruff shampoos and sunscreens, monitor the more than 10,000 drugs on the market to be sure they continue to meet the highest standards, monitor TV, radio, and print drug ads to ensure they are truthful and balanced and provide health professionals and consumers information to use drugs appropriately and safely.

klinks novartis vaccins zijn levensgevaarlijk

En de Novatis vaccins bevatten de hulpstof MF59 ofwel squaleen. update squaleen

Over andere ingrediënten later meer.

vaccines - dispelling vaccination myths with truths

Myth No. 1: Vaccines are safe

Under the 1986 National Childhood Vaccine Injury Act, VAERS (Vaccine Adverse Reporting System) was established. Annually, it reports about 11,000 serious vaccine reactions, including up to 200 deaths and many more permanent disabilities.

Far more alarming is the following;

-- the FDA estimates that only 1% of serious adverse reactions are reported;

-- CDC says it's 10%;

-- medical school students testified before Congress that they're told not to report these incidents;

-- according to the National Vaccine Information Center (NVIC), only one in 40 New York doctors reported adverse vaccine reactions or deaths;

-- international studies show vaccines cause up to 10,000 US SIDS (Sudden Infant Death Syndrome) deaths annually, and at least half of them are from vaccines;

-- another study determined that 3000 US children die annually from vaccines;

-- poor reporting in America suggests that annual adverse vaccine reactions, in fact, number from 100,000 - one million;

-- since 1988, the government's National Vaccine Injury Compensation Program (NVICP) paid families of affected children $1.2 billion in damages;

-- as authorized by the 2006 Public Readiness and Emergency Preparedness (PREP) Act, HHS Secretary Sebelius, granted drug companies legal immunity (except for impossible to prove willful misconduct) to proliferate dangerous, untested Swine Flu vaccines globally;

-- vaccines are legally mandated in all 50 US states, though legally avoidable in most (under normal circumstances) as explained below;

-- in settling vaccine damage suits, drug companies impose gag orders to keep vital information from the public; and

-- insurers refuse to cover adverse vaccine reactions because of the high potential liability they'd face.

Truth No. 1

Vaccinations cause high numbers of severe reactions, permanent disabilities, and deaths as well as an enormous personal and public cost. Virtually none of this gets reported.

Myth No. 2: Vaccines are very effective

Medical literature documents significant numbers of vaccine failures for measles, mumps, small pox, pertussis, polio and Hib-causing bacterial meningitis and pneumonia. In 1989, Oman experienced a widespread polio outbreak six months after completing a population-wide immunization program. In Kansas (in 1986), 90% of 1300 reported pertussis cases were "adequately vaccinated," and 72% of Chicago pertussis incidents in 1993 had been as well.

Truth No. 2

Evidence shows that vaccinations are an unreliable and dangerous way to prevent illness and disease.

Myth No. 3: Low US disease rates are attributable to vaccines

From 1850 - 1940, well before mandatory vaccination programs, the British Association for the Advancement of Science reported a 90% decrease in childhood diseases due to improved sanitation and hygiene practices. By 1945, US medical authorities noted a 95% drop in deaths from the leading childhood infectious diseases (diphtheria, pertussis, scarlet fever and measles), well before mass-immunizations began.

A recent WHO report found that third world disease and mortality rates had no direct correlation with immunization programs, but closely relate to hygiene and diet standards.

Truth No. 3

No evidence links vaccines with infectious disease declines. Proper hygiene and diet practices may be far more effective.

Myth No. 4: Sound immunization theory and practice prove the effectiveness of vaccines

Although vaccines stimulate antibody production, no evidence suggests that alone assures immunity. A 1950 British Medical Council-published study found no relationship between antibody count and disease incidence. Natural immunization involves many bodily organs and systems. Artificially producing antibodies can't achieve it.

Research also shows how squalene adjuvants harm the human immune system, making it susceptible to numerous illnesses and diseases ranging from very annoying to life threatening. In addition, the "herd immunity" notion of mass-immunizations effectiveness is largely discredited. Just the opposite is true as evidence shows that fully vaccinated populations have experienced epidemics numerous times in the past.

Further, vaccine effectiveness "remains scientifically unproven" because no double blind studies have been conducted to do it. Significantly, recent disease outbreaks have affected more vaccinated children than unvaccinated ones. And the common practice of "one size fits all" is troublesome. It lets tiny new-borns get the same dosage as a five year old. It tolerates dubious quality control practices producing what's known as "Hot Lots" - ones associated with disproportionately high death and disability rates.

Shockingly, the FDA refuses to act preventatively against them. In fact, individual vaccine lots have almost never been recalled even when associated with severe adverse reactions. Instead, they're administered under the assumption that all recipients respond the same, regardless of race, ethnicity, genetic makeup, or other characteristics.

A recent New England Journal of Medicine-reported study found that a significant number of Romanian children receiving polio vaccine contracted the disease. Evidence linked antibiotic injections to it. One innoculation raised the polio risk eight-fold; two - nine shots, 27-fold, and 10 or more 182-fold.

New research may reveal other unknown hazards, but public safety won't be addressed until government health officials act responsibly, report accurately, and adequately protect their populations from vaccines they never should allow.

Truth No. 4

Many supposed vaccine truths have, in fact, been proved false.

Myth No. 5: Childhood diseases are extremely dangerous

False. Even CDC data show a 99.8% pertussis recovery rate during the 1992-94 period. One Cincinnati Children's Hospital infectious diseases expert said at the time: "The disease was very mild, no one died, and no one went to the intensive care unit."

Nearly always, childhood infectious diseases "are benign and self-limiting. They usually impart lifelong immunity, whereas vaccine-induced immunization (when achieved) is only temporary." In fact, it can increase vulnerability later on by postponing better tolerated childhood illnesses until adulthood when death rates (though still low) are far higher.

Most important is that nearly all common infectious diseases are rarely dangerous, and, in fact, can develop strong, healthy adult immune systems when they're most needed. In addition, few people know that children who didn't contract measles have a higher incidence of skin diseases, degenerative bone and cartilage ones, and tumors while ovarian cancer is higher among mumps-free adult women. The human immune system benefits from common childhood infectious diseases. Freedom from them may be harmful later on.

Truth No. 5

Childhood disease dangers are greatly exaggerated to scare parents into getting their children vaccinated with unsafe drugs.

Myth No. 6: Polio vaccinations were very successful

False again. In 1955, when the Salk vaccine was introduced, polio was considered the most serious post-war public health problem. A year later, six New England states reported sharp rises ranging from more than double in Vermont to a 642% increase in Massachusetts. Other states also were badly impacted enough for Idaho and Utah to halt immunizations due to increased incidence and death rates.

In his 1962 congressional testimony, Dr. Bernard Greenberg, Biostatistics Department head at the University of North Carolina, reported sharp polio increases from 1957 to 1959 and a Public Health Service whitewash that suppressed it. In 1985, the CDC reported that 87% of US cases between 1973 and 1983 were caused by the vaccine. Later it added that it caused nearly all imported cases, and most of the victims were fully vaccinated.

Further, misdiagnosing, poor reporting, and cover-ups suggest that the actual number of vaccine-associated paralytic polio (VAPP) cases "may be 10 to 100 times higher than that cited by the CDC."

In 1977, even Jonas Salk admitted that mass inoculations caused most polio cases since 1961.

Truth No. 6

The Salk vaccine proved highly dangerous. Information about it was suppressed, and declines in the disease were well underway when mass-immunizations were begun. In Europe, they occurred in countries that used, then rejected the vaccine proving it was never needed in the first place. Showing also that the same is true for other diseases, including Swine Flu with the WHO and CDC admitting that most cases are mild, unthreatening, and generally pass without treatment, let alone risking dangerous unneeded vaccines.

Myth No. 7: Lack of an initial adverse reaction proves vaccines are safe

Documented long-term health problems include arthritis, chronic headaches, rashes indicative of disease, non-healing skin lesions, seizures, autism, anemia, multiple sclerosis, ALS, cancer, and many others. Ingredients common to all vaccines are at issue. Squalene adjuvants are a biological time bomb that can harm or destroy the human immune system.

Other ingredients are known toxicants and carcinogens, including thimersol (a mercury derivative), aluminum phosphate, formaldehyde, phenoxyethanol, and numerous gastrointestnal toxicants like liver toxicants, cardiovascular and blood toxicants, and reproductive toxicants. "Chemical ranking systems rate many vaccine ingredients among the most hazardous substances" known, even in microscopic doses.

"Millions of children (and adults) are partaking in an enormous crude experiment, and no sincere, organized effort is being made to track the negative side effects or to determine the long-term consequences."

Dr. Bart Classen's epidemiological research found vaccines as the cause of 79% of insulin type I diabetes cases in children under 10. The sharp rise in numerous other diseases may also be linked with mass-immunizations. California's autism rate skyrocketed 1000% in the last 20 years. In the 1990s, MMR vaccine usage in Britain (for measles, mumps and rubella) occurred at the same time autism rose sharply. The January 2000 Journal of Adverse Drug Reactions reported that no adequate testing was done, so the vaccine never should have been licensed.

The Autism Society says: "Autism is a complex developmental disability that typically appears during the first three years of life and is the result of a neurological disorder that affects the normal functioning of the brain...."

According to the CDC and National Vaccine Information Center, one in every 150 US children develop the disease. Tens of millions are affected worldwide, making it more common than pediatric cancer, incurable type 1 (juvenile-onset) diabetes and AIDS combined. In the early 1940s, prior to mass immunizations, autism was so rare that few doctors ever encountered it. Today it's a global pandemic.

Truth No. 7

Long-term vaccination reactions have been suppressed and ignored in spite of the alarming correlation between their use and the rise of autoimmune and other diseases. Vaccines aren't for protection. They're for profit and other nefarious purposes. Avoiding them is essential to protecting human health and well-being.

Myth No. 8: Vaccines are the only available disease prevention option

"Historically, homeopathy has proven many times...more effective than allopathic (conventional) medicine in the treatment and prevention of disease." During the 1849 US cholera outbreak, homeopathic hospitals documented a 3% death rate compared to 48 - 60% in conventional ones. It's as true today, and recent epidemiological studies show homeopathic remedies far superior to vaccines in preventing diseases. They're safe, effective, and toxin and side effect-free, yet most insurers won't cover them.

Truth No. 8

Alternative treatments and remedies have been safe and effective for generations, yet the medical establishment and governments attack and spurn them.

Myth No. 9: "Vaccinations are legally mandated and unavoidable..."

All states require them. However, laws vary by state, legal exemptions exist, and all states offer one or more of the following:

-- all states allow medical exemptions for persons susceptible to adverse reactions; parents can cite this for their children based on family history;

-- 48 states offer religious exemptions but may require membership in an established religious organization; "according to federal precedent, personal religious beliefs may be sufficient for a religious exemption regardless of which religious organization you belong to, or whether or not you belong to an organized religion at all;" in addition, the Supreme Court defined religion broadly for legal purposes; and

-- 17 states allow philosophical or personal exemptions.

All public and private schools must comply with federal and state vaccination laws and permit legal exemptions.

Truth No. 9

Some vaccines are mandated, but most, perhaps all, US citizens may use legal exemptions to avoid them. In a recent article, however, Phillips states:

"All non-medical exemptions in the US are ultimately provided conditionally. That is, states have the right to require immunization for everyone, legally exempt or not, during an (emergency) outbreak, other than (for) those" with medical exemptions.

Myth No. 10: Governments place public health concerns above all others

Vaccination history shows "documented instances of deceit portraying vaccines as mighty disease conquerors, when in fact vaccines have had little or no discernible impact - or have even delayed or reversed - pre-existing disease declines....Conflicts of interest are the norm in the vaccine industry." Government agencies like the FDA and CDC are stacked with corporate officials who return to high-paying industry jobs provided they place profit considerations over public health and safety.

In November 2000, concern over this and adverse reactions got the American Association of Physicians and Surgeons (AAPS) to pass a unanimous resolution at its 57th meeting calling for a moratorium on mandatory childhood vaccinations and for doctors to insist on "truly informed consent for (their) use...."

In October 1999, Dr. Bart Classen, founder and CEO of Classen Immunotherapies, told Congress:

"It is clear....that the government's immunization policies are driven by politics and not by science. I can give numerous examples where employees of the US Public Health Service....appear to be furthering their careers by acting as propaganda officers to support political agendas. In one case....employees of a foreign government, who were funded and working closely with the US Public Health Service, submitted false data to a major medical journal. The true data indicated the vaccine was dangerous; however, the false data" indicated no risk.

In addition, "four letters from the FDA/Public Health Service....clearly reveal(ed) that the anthrax vaccine" approved for US military personnel was done "without the manufacturer performing a single controlled clinical trial." They're essential to determine safety and effectiveness. Failure to conduct them proved devastating to the health and well-being of recipients and still does today. Besides, all vaccines are unsafe and some are extremely dangerous.

US military forces receive many or all of the following vaccinations:

-- three shots for hepatitis B;

-- two for hepatitis A;

-- annually for influenza so all military personnel will get Swine Flu shots;

-- all military personnel must have documented proof of receiving MMR vaccines for measles, mumps and rubella; those without them them get single doses;

-- two varicella (chicken pox) shots;

-- smallpox doses every ten years;

-- three for polio for adults never vaccinated; those fully vaccinated get a booster shot;

-- tetanus-diphtheria and pertussis vaccinations for personnel who haven't have them in the past 10 years;

-- tetanus every 10 years;

-- typhoid vaccinations in either oral or injectable forms;

-- a multiple dose series for anthrax;

-- yellow fever every 10 years in some cases;

-- three for rabies and later boosters;

-- tuberculosis screening and shots;

-- single pneumococcal doses;

-- meningococcal vaccinations every five years before deployment to certain regions; and

-- three Japanese encephalitis doses in some cases.

Multiple vaccinations for all US military personnel practically assures damage to their immune systems and severe health problems later on.

Truth No. 10

Public health officials approve dangerous vaccines on unsuspecting recipients and profit handsomely for their efforts.

Final Comments

All vaccines are biological weapons that weaken or destroy the human immune system. They often fail to protect against diseases they're designed to prevent and often cause them. The H1N1 vaccine is experimental, untested, toxic, extremely dangerous, and essential to avoid even if mandated.

In a December 1994 Medical Post article, Dr. Guylaine Lanctot said:

"The medical authorities keep lying. Vaccination has been a disaster on the immune system. It actually causes a lot of illnesses. We are actually changing our genetic code through vaccination....100 years from now we will know that the biggest crime against humanity was vaccines."

Dr. Viera Scheibner is internationally known as perhaps the leading expert on adverse vaccine reactions. Her analysis concluded that "there is no evidence whatsoever of the ability of vaccines to prevent any diseases. To the contrary, there is a great wealth of evidence that they cause serious side effects."

Nonetheless, immunization programs proliferate because the profit potential is enormous despite growing numbers of reputable scientific figures citing concerns.

Currently, over 200 new vaccines are being developed "for everything from birth control to (curbing) cocaine addiction." Around half of them are in clinical trials using human guinea pigs putting their health and safety on the line unwittingly.

New delivery systems are also being developed that include nasal sprays, mosquitoes, and genetically engineered fruits containing vaccine viruses. With every country in the world a potential buyer, health and safety considerations are suppressed for the sake of profits. Unless somehow this madness is stopped, the harm to our children and society will be catastrophic.

Stephen Lendman is a Research Associate of the Centre for Research on Globalization. He lives in Chicago and can be reached at lendmanstephen@sbcglobal.net.

Also visit his blog site at sjlendman.blogspot.com and listen to The Global Research News Hour on RepublicBroadcasting.org Monday - Friday at 10AM US Central time for cutting-edge discussions with distinguished guests on world and national issues. All programs are archived for easy listening.

vogelvrij bij weigeren vaccin

The World Health Organization determined in 2005 it has the authority to dissolve sovereign governments and take control should there be a “pandemic”. This applies to any country signed onto WHO….which of course we are. The WHO just raised this non-existent pandemic to level 4.

From the WHO 2005 declaration: (excerpted)

“Under special pandemic plans enacted around the world including the USA, in 2005, national governments are to be dissolved in the event of a pandemic emergency and replaced by special crisis committees, which take charge of the health and security infrastructure of a country, and which are answerable to the WHO and EU in Europe and to the WHO and UN in North America.

If the Model Emergency Health Powers Act is implemented on the instructions of WHI, it will be a criminal offence for Americans to refuse the vaccine. Police are allowed to use deadly force against “criminal” suspects. Here are ten key points associated with MSEHPA:

Under the Model State Emergency Health Powers Act, upon the declaration of a “public health emergency,” governors and public health officials would be empowered to:

1. Force individuals suspected of harboring an “infectious disease” to undergo medical examinations.
2. Track and share an individual’s personal health information, including genetic information.
3. Force persons to be vaccinated, treated, or quarantined for infectious diseases.
4. Mandate that all health care providers report all cases of persons who harbor any illness or health condition that may be caused by an epidemic or an infectious agent and might pose a “substantial risk” to a “significant number of people or cause a long-term disability.” (Note: Neither “substantial risk” nor “significant number” are defined in the draft.)
5. Force pharmacists to report any unusual or any increased prescription rates that may be caused by epidemic diseases.
6. Preempt existing state laws, rules and regulations, including those relating to privacy, medical licensure, and–this is key–property rights.
7. Control public and private property during a public health emergency, including pharmaceutical manufacturing plants, nursing homes, other health care facilities, and communications devices.
8. Mobilize all or any part of the “organized militia into service to the state to help enforce the state’s orders.” Ration firearms, explosives, food, fuel and alcoholic beverages, among other commodities.
9. Impose fines and penalties to enforce their orders.

So there you have it. You are now officially to be declared a criminal if you refuse the vaccine and deadly force can be used against you if you resist. And to think, not only did our federal government agree to this abomination, it was also successful in getting the same laws passed in most states. I will be revisiting this list of powers in a subsequent article as it relates to the coming “healthcare reform”, and other odious pieces of legislation being devised.

This gives me pause to consider this: Could the so-called healthcare reform that the government claims must be done right away, right now, quickly, immediately….no time to waste be tied somehow to this WHO declaration? Hmmmm. I smell a really big rat!

---

Those pesky FEMA drills…part of a plan?

I am wary of this FEMA drill that is taking place not only for the obvious reasons….but its close proximity to the planned forced vaccinations scheduled to be mandated early this fall. Our own government has expressed its intent to forcibly vaccinate school children as a starter. By all means…..target the most vulnerable first. (Take that any way you like.)

On MSM last evening it was reported that young people between the ages of 19 and 24 are for some reason most susceptible to this lab created virus. I find this curious as this segment of the population is generally the healthiest. Since the “swine” flu has been so thoroughly exposed as lab created they are now just simply calling it the N1 whatever flu. Apparently this first test run of what was supposed to be a global pandemic couldn’t get off the ground: it didn’t spread as was hoped. Of course the same thing happened with SARS and the Bird Flu…..Those didn’t work so now we get the “Swine Flu”, or the N1 Whatever Flu”.

Strange how all these flu’s showed up after they dug up bodies from mass graves to see if they really did die from the flu epidemic in 1918. The new and improved version of this virus is now what we are calling N1 Whatever Flu.

Here’s what I believe is about to happen:

A created strain of flu is going to be set loose in selected areas to begin with. As I believe thousands are going to fall ill simultaneously it will be the fear factor needed to bring thousands more in for what they believe is a vaccine that will save them. Those that want to self-quarantine, or who simply refuse the vaccines, will either be incarcerated in FEMA camps or otherwise disposed.

The vaccines which have not been tested for safety or effectiveness can and will cause harm to many of those receiving the shots, but will be off limits to lawsuits for harm caused. This will force thousands more in for the vaccinations, out of fear, which are loaded with toxins and pathogens seeking to save themselves from forced incarceration or worse. At some point in this, we will find out that the foreign troops who supposedly only participated in a mock drill, are not only still here on our soil, but their numbers have multiplied.

Martial law will be declared using the unilateral authority granted the president under the John Warner Defense Authorization Act of 2007, which allows the president to declare an emergency “even if he is the only person to perceive one”. Foreign troops lack the natural inhibition our own military has about firing on US citizens…that’s why they are here. I do not believe this is a mock drill. I think it is actually the planned strategic placement of foreign troops within the US for an anticipated and planned event.

The vented three story rail cars which are claimed to be nothing more than haulers for large SUV type vehicles would come in really handy here. Foreign troops and military equipment could be moved further into the country and put in place without anyone ever knowing they were there until they were needed. Besides, I don’t know of any car haulers that need that much targeted ventilation: humans on the other just might.

I feel that there will be several catastrophic events from about mid-August to the end of October and maybe into November somewhat. At the end of this period, after the American public has been frightened to death, everything will begin coalescing and will culminate at the end of the year.

In the interim: will we see the deaths of thousands upon thousands of American’s and other peoples around the world, if not millions?

I was curious as to why the WHO would move this flu into a pandemic (phase 4) category when there was no evidence that it was pandemic.

(Two weeks ago, WHO advised nations to stop testing for H1N1 and instead to report trends of flu like symptoms.) H1N1 has been very mild, according to the WHO:

“This pandemic has been characterized, to date, by the mildness of symptoms in the overwhelming majority of patients, who usually recover, even without medical treatment, within a week of the onset of symptoms.”

Then came the predictions from our government that the “flu” would probably become much worse this fall. This indicates to me that a new and more virulent strain has been developed and is set to be turned loose. I base this on the evidence that the flu was lab created and would not have occurred naturally combining four unrelated dna strains……the statements by the CDC that they had a vaccine within three weeks of the “outbreak”…..knowing that seed stock for vaccines takes at least 12 weeks to develop and several more weeks to mass produce……and the orders during the last year of the Bush Crime Administration for Tamiflu which supposedly is the cure or prevention for a flu which didn’t exist at the time, at least not publicly.

Whatever has been in the works for several years, if not for decades is about to come to fruition. Grab your butts! This is going to be one bumpy ride!

(C) 2009 Marti Oakley July 30, 2009 - Farm Wars

squaleen laat u liefst niet in uwe aderen spuiten

WHO claimt dat hulpstof squaline veilig is. Het is echter niet zo.

- "animals injected with his formulation developed terrible, incurable conditions: allergic aspermatogenesis (stoppage of sperm production), experimental allergic encephalomyelitis (the animal version of MS), allergic neuritis (inflammation of the nerves that can lead to paralysis) and other severe autoimmune disorders". There was no reversing any of these conditions.

Met name die verlammingen en autoimmuumziekten kom ik overal tegen. Bijvoorbeeld de duizenden claims van mensen die de swineflu injectie in jaren '70 hebben genomen, handelen grotendeels over verlammingen.

Uit "Vaccine A" van Gary Matsumoto:

"It does a terrific job of stimulating the immune system, though. Unfortunately, Freund's Complete Adjuvant can cause permanent organ damage and incurable disease. As early as the 1930s, these oil additives were notorious for inducing illness. By the 1950s, scientists knew these illnesses were specifically autoimmune. Today that is their chief use in research—inducing disease instead of preventing it. Scientists studying autoimmune disease cannot wait around for its spontaneous appearance in a lab animal; they inject it with Freund's Complete Adjuvant to reproduce autoimmunity on demand. Oil adjuvants made with squalene equally effective at this job, and regrettably according to Dutch scientists, equally inhumane." (ik weet niet wie deze "Dutch scientists" zijn)

---

"The UCLA team had found what it was looking for: oils that induced autoimmune disease, but with less inflammation. Between the two of them, squalene was less desirable for UCLA's purposes. "Squalene was more arthritogenic," Beck recalls, "but it also produced a greater inflammation."

Link naar exerpt, "The Greatest Story Never Told"

IV

vaccines far more deadly than swine flu

gedegen raport - geen conspiracy lulkoek.

HGR