Showing posts with label World Health Organization. Show all posts
Showing posts with label World Health Organization. Show all posts

Friday, July 31, 2009

Is forced vaccination with an experimental flu vaccine possible in America?

Is forced vaccination with an experimental flu vaccine possible in America?

On June 11, 2009 the World Health Organization (WHO) of the United Nations declared a “Level 6” influenza pandemic, setting in motion the race to create a vaccine to “prevent the spread” of the novel H1N1 flu virus. Why the rush to create a vaccine when WHO figures reveal that five million have a severe case of the seasonal flu and an estimated 250,000 to 500,000 die annually despite record levels of flu vaccine produced and distributed last year? As of July 6, 2009, the WHO has cited 94, 512 cases and 429 deaths attributed to the new H1N1 flu virus worldwide. This is a fraction of cases and deaths attributed to the seasonal flu each year. The WHO claims the number of cases and deaths are growing exponentially and decided to not make these figures available once the number of cases reached 100,000.

*Our country is preparing for mass flu shots this fall. There is a 99% probability that the new pandemic vaccine in production will be mandatory. HHS Secretary Kathleen Sebelius has ordered 600 million doses of swine (H1N1) vaccine, two doses for nearly every man, woman and child in the U.S.

*State epidemiologists are recommending two doses of the pandemic vaccine in addition to the seasonal flu shot. State officials are slated with the task of maintaining public confidence in the pandemic flu vaccine program since serious adverse reactions are anticipated.

*The pandemic vaccine in production will contain an untested oil-in-water adjuvant (boosts antibody production) in order to create millions of doses from a small quantity of the alleged novel H1N1 virus.

*Investigative journalist Gary Matsumoto in his book, Vaccine A: The Covert Government Experiment That's Killing Our Soldiers and Why GIs Are Only the First Victims, the results of clinical trials of oil based adjuvants on lab animals tested at Fort Detrick, Maryland. After all lab animals suffered from severe arthritis and autoimmune disorders prior to a premature death, scientists concluded that an oil based adjuvant should never be used in vaccines intended for humans. Despite this strong evidence, thousands of U.S. soldiers, beginning with Gulf War I, have been given anthrax vaccines containing varying amounts of the oil-based adjuvant, squalene. Many researchers have linked Gulf War Illness with the anthrax vaccines administered to our soldiers since many of those diagnosed were never deployed overseas. However, the Pentagon has ignored the problem, denied many veteran’s benefits and only publicly acknowledged the existence of Gulf War Illness in 2008.

*The Biodefense and Pandemic Vaccine and Drug Development Act of 2006 (also known as BioShield 2) strips Americans of the right to a jury trial if harmed by an experimental drug or vaccine they are forced to take if WHO or government officials declare a public health emergency. Learning from the 1976 swine flu fiasco where hundreds of vaccine recipients got Guillain Barre Syndrome (paralysis) or died, our own government wrote liability protection into the Act, if vaccine-related damage occurs.

This provision gives our government and pandemic vaccine manufacturers no reason to create safe or effective vaccines or other counter-measure drugs for use in a declared emergency.

*Forced mandatory vaccination is akin to medical experimentation against a person's will. Without informed consent, this is a violation of two international agreements: The Nuremberg Code and the World Medical Association Declaration of Helsinki.

*HHS Secretary Sebelius has called on school superintendents to spend their summer turning their schools into vaccination clinics for the incoming students this fall. Anticipating a short supply of vaccine initially, target populations in order of priority are
(1) all students and staff associated with schools (K-12th grade) and children (aged 6 months or older) and staff in child care centers,
(2) Pregnant women, children 6 months to 4 years of age, new parents and household contacts of children,
(3) Adults less than 65 years old with medical conditions that increase the risk of complications from influenza, and
(4) Health care workers and emergency services sector personnel.

Questions to ask your governor, state legislators, sheriff,
County commissioners and emergency response personnel:


•Will state vaccine exemption laws apply if my child goes to school and they are vaccinating the school's staff and students with the pandemic flu vaccine?
•Will informed and voluntary consent be obtained from parents prior to the administration of a seasonal or pandemic flu vaccine?
•Will our right to decline these shots based on our religious beliefs, or for health reasons – such as severe allergies/anaphylaxis to normal vaccine ingredients - be honored?

Many innovative alternative health companies have produced safe products that have worked successfully in preventing and/or minimizing the annual flu according to the experiences of thousands of consumers. The FDA recently spent their resources targeting any company who dared to make claims that their product may reduce the possibility of contracting the swine flu or minimizing symptoms.

Why does the FDA spend resources targeting products with better track records than the swine flu vaccine in production that will cost billions in federal taxpayer dollars and is anticipated to cause severe adverse effects? Furthermore, why would the manufacturers of the swine flu vaccine and our own federal government be immune from liability should death or injury occur as a result of the vaccine?

The CDC has admitted that 71% of all hospitalizations for swine flu were among those who were chronically ill, such as undergoing chemotherapy or suffering from an autoimmune disorder. In one hospital in Michigan, 9 out of 10 swine flu patients were obese and 2 out of 3 who died were severely obese.

Instead of focusing on risk factors and targeting those populations most at risk for contracting and dying from the swine flu, the CDC has targeted children in school and childcare facilities and their staff to be the first to receive the experimental vaccine. Can you explain to us why the CDC is continually diverting our attention from the real epidemics of obesity, cancer and autoimmune diseases plaguing our country that are clearly risk factors in contracting the new swine flu and, instead, targeting our children to be the first to receive the pandemic flu vaccine?

Our country and the world are experiencing an economic depression. Many states are bankrupt and the numbers of unemployed and homeless people increase daily. Meanwhile, our Congress continues to pass legislation exacerbating the economic woes of our country rather than being part of the solution. How will the expenditure of billions of tax dollars for manufacturing, storing, and disseminating an untested, experimental vaccine solve our healthcare and economic crises? Isn't the current proposed mass vaccination plan a clear violation of the 4th Amendment to the Constitution?

For more information, go to PandemicFluOnline.com and VaccineTruth.com CopyRound©

Vaccine may be more dangerous than the swine flu

Vaccine may be more dangerous than the swine flu
(As published in the Idaho Observer.)


One can continue to believe that the global gurus of public
health are responding appropriately to the swine flu emergency and willingly take the shot if they choose to do so. But such trust and complacency requires the omission of one key factiod: The vaccine contains an oil-based “adjuvant” containing “squalene.” Adjuvants are used to boost an immune response. Squalene, which is a causal factor in Gulf War illness, causes crippling arthritis and
premature death in about 100 percent of lab animals and has been associated with autoimmune diseases and premature death in people as well. Early reports of trials with the H1N1 vaccine show that the vaccine is already maiming and killing people. It appears certain that those who take the vaccine may not get the flu but can expect to die a painful and premature death—and WHO et. al know it.

By Dr. Russell Blaylock

An outbreak of swine flu that occurred in Mexico last spring eventually affected 4,910 Mexican citizens and resulted in 85 deaths. By the time it spread to the United States, the virus caused only mild cases of flu-like illness. Thanks to air travel and the failure of public health officials to control travel from Mexico, the virus spread worldwide. Despite predictions of massive numbers of deaths and the arrival of doomsday, the virus has remained a relatively mild disease, something we know happens each year with flu epidemics.

Cases to date as of July 7, 2009. Worldwide, there have only been 311 deaths out of 70,893 cases of swine flu. In the United States, 27,717 cases have resulted in 127 deaths. Every death is a tragedy, but such a low death rate should not be the basis of a draconian government policy.

It is helpful to recall that the Centers for Disease Control, with the collusion of the media, constantly tell us that 36,000 people die from the flu each year, a figure that has been shown to be a lie. In this case, we are talking about 300 plus deaths for the entire world.

From whence this novel strain?
This virus continues to be an enigma for virologists. In the April 30, 2009 edition of Nature, a virologist was quoted as saying, ”Where the hell it got all these genes from we don’t know.” Extensive analysis of the virus found that it contained the original 1918 H1N1 flu virus, the avian flu virus (bird flu) and two new H3N2 virus genes from Eurasia. Debate continues over the possibility that swine flu is a genetically-engineered virus.

Scandal. Naturally, vaccine manufacturers have been in a competitive battle to produce the first vaccine. The main contenders have been Baxter Pharmaceuticals and Novartis Pharmaceuticals, the latter of which recently acquired the scandal-ridden Chiron vaccine company. Both of these companies have had agreements with the World Health Organization to produce a pandemic vaccine.

Contamination. The Baxter vaccine, called Celvapan, has had fast track approval. It uses a new vero cell technology, which utilizes cultured cells from the African green monkey. This same animal tissue transmits a number of vaccine-contaminating viruses, including the HIV virus.

More contamination. The Baxter company has been associated with two deadly scandals. The first event occurred in 2006 when hemophiliac components were contaminated with HIV virus and injected in tens of thousands of people, including thousands of children. Baxter continued to release the HIV contaminated vaccine even after the contamination was known.

Accidental release.
The second event occurred recently when it was discovered that Baxter had released a seasonal flu vaccine containing the bird flu virus, which would have produced a real world pandemic, to 18 countries. Fortunately, astute lab workers in the Czech Republic discovered the deadly combination and blew the whistle before a worldwide disaster was unleashed [The IO, March, 2009]. Despite these two deadly events, WHO maintains an agreement with Baxter Pharmaceuticals to produce the world’s pandemic vaccine.

[Note: WHO announced that it would launch an investigation into Baxter’s “accidental” release of H5N1-contaminated flu vaccine that killed lab animals (ferrets) in the Czech Republic. No investigation has ever been conducted. ~DWH].

Squalene

Novartis, the second contender, also has an agreement with WHO for a pandemic vaccine. Novartis appears to have won the contract, since its vaccine is near completion. What is terrifying is that these pandemic vaccines contain ingredients, called “immune adjuvants” that a number of studies have shown cause devastating autoimmune disorders, including rheumatoid arthritis, multiple sclerosis and lupus.
Animal studies using this adjuvant have found them to be deadly. A study using 14 guinea pigs found that, when they were injected with the special adjuvant, only one animal survived. A repeat of the studyfound the same deadly outcome.
So, what is this deadly ingredient? It is called squalene, a type of oil. The Chiron company, maker of the deadly anthrax vaccine, makes an adjuvant called MF-59 which contains two main ingredients of concern—squalene and gp120. A number of studies have shown that squalene can trigger all of the above-mentioned autoimmune diseases when injected.

[Note: All higher organisms produce squalene. The squalene used as a vaccine adjuvant is a fish oil, particularly shark liver oil. The problem with injected squalene is that it signals the body to attack its own essential fatty acids. Combined with other vaccine ingredients, the result is autoimmunity, where
the body begins attacking its own tissues. ~DWH]


The MF-59 adjuvant has been used in several vaccines. These vaccines, including tetanus and diphtheria, are the same vaccines frequently associated with adverse reactions.

Questionable studies. I reviewed a number of studies on this adjuvant and found something quite interesting. Several studies done on human test subjects found MF-59 to be a very safe immune adjuvant. But when I checked to see who did these studies, I found—to no surprise—that they were done by the Novartis Pharmaceutical Company and Chiron Pharmaceutical Company, which have merged. They were all published in “prestigious” medical journals. Also, to no surprise, a great number of studies done by independent laboratories and research institutions all found a strong link between MF-59 and autoimmune diseases.

Gulf War Illness. Squalene in vaccines has been strongly linked to the Gulf War Illness. On August 1991, Anthony Principi, Secretary of Veterans Affairs, admitted that soldiers vaccinated with the anthrax vaccine from 1990 to 1999had an increased risk of 200 percent in developing the deadly disease amyotrophic lateral sclerosis (ALS), also called Lou Gehrig’s disease. The soldiers also suffered from a number of debilitating and life-shortening diseases such as polyarteritis nodosa, multiple sclerosis (MS), lupus, transverse myelitis (a neurological disorder caused by inflammation of the spinal cord), endocarditis (inflammation of the heart’s inner lining), optic neuritis with blindness and
glomerulonephritis (a type of kidney disease).

Brain inflammation. Because squalene, the main ingredient in MF-59, can induce hyperimmune responses and induce autoimmunity, a real danger exists for prolonged activation of the brain’s immune cells, the microglia. This type of prolonged activation has been strongly associated with such diseases as multiple sclerosis, Alzheimer’s disease, Parkinson’s disease, ALS and possibly vaccine-related encephalitis. It has been shown that activation of the systemic immune system, as occurs with vaccination, rapidly activates the brain’s microglia at the same time, and this brain inflammation can persist for long periods.

So, how would the gp120 get into the brain? Studies of other immune adjuvants using careful tracer techniques have shown that they routinely enter the brain following vaccination. What most people do not know, even the doctors who recommend the vaccines, is that most such studies by pharmaceutical companies observe the patients for only one to two weeks following vaccination—these types of reactions may take months or even years to manifest.

The profit motive
It is obvious that the vaccine manufacturers stand to make billions of dollars in profits from this WHO/government-promoted pandemic. Novartis, the maker of the new pandemic vaccine, recently announced that they would not give free vaccines to impoverished nations—everybody pays.

Grim reality. One must keep in mind that once the vaccine is injected, there is little you can do to protect yourself—at least by conventional medicine. It will mean a lifetime of crippling illness and early death.

The best medicine. There are much safer ways to protect oneself from this flu virus, such as higher doses of vitamin D3, selective immune enhancement using supplements and a good diet.

Dr. Russell Blaylock, is a board certified neurosurgeon, author and lecturer. An
expert on nutrition, aspartame, MSG and vaccines, he is also editor of the widely
distributed Blaylock Wellness Report.

Note: The subheads and boldface preceding certain paragraphs were added to the original text to highlight the ground Dr. Blaylock is covering in this brief article. Each point he makes could be books in themselves but his intent was to show that the much publicized “novel” flu strain was likely created in a lab by entities connected to the scandal-ridden pharmaceutical companies being rewarded with huge contracts to produce millions (billions) of vaccines that contain a specific ingredient known to cause chronic illnesses and early death.

The most comprehensive journalistic investigation on the politics and effects of squalene is “Vaccine A: The Covert Government Experiment That’s Killing Our Soldiers and Why GIs Are Only the First Victims” by Gary Matsumoto (2004). The book can be ordered online or through your local bookseller.

Military Poised to Help FEMA Battle Swine Flu Outbreak...what happens if we refuse to take it? Martial law?

Military Poised to Help FEMA Battle Swine Flu Outbreak...what happens if we refuse to take it? Martial law?

The Advisory Committee on Immunization Practices voted to set vaccination priorities for certain groups Wednesday during a meeting in Atlanta as the Pentagon prepares to help the Federal Emergency Management Agency tackle a potential outbreak of the H1N1 virus this fall.

The Pentagon is preparing to make troops available if necessary to help the Federal Emergency Management Agency tackle a potential outbreak of the H1N1 virus this fall, FOX News has confirmed.

This comes as a government panel recommends certain groups be placed at the front of the line for swine flu vaccinations this fall, including pregnant women, health care workers and children six months and older.

The Advisory Committee on Immunization Practices panel also said those first vaccinated should include parents and other caregivers of infants; non-elderly adults who have high-risk medical conditions, and young adults ages 19 to 24. The panel, whose recommendations typically are adopted by federal health officials, voted to set vaccination priorities for those groups Wednesday during a meeting in Atlanta.

Obama administration officials told Congress that H1N1 vaccinations won't be available for several months.

Defense Secretary Robert Gates is preparing to sign an order authorizing the military to set up five regional teams to deal with the potential outbreak of H1N1 influenza if FEMA requests help.

A senior U.S. defense official told FOX News that the plan calls for military task forces to work in conjunction with the FEMA. No final decision has been reached on how the military effort would be manned, but one source said it likely would include personnel from all branches of the military.

It is not known how many troops would be needed and whether they would come from the active duty or the National Guard and Reserve forces.

In the event of a major outbreak, civilian authorities would lead any relief efforts, the official said. The military, as it would for a natural disaster or other significant emergency situation, could provide support and fulfill any tasks that civilian authorities could not, such as air transport or testing of large numbers of viral samples from infected patients.

As a first step, military leaders have asked Gates to authorize planning for the potential assistance.

Orders to deploy actual forces would be reviewed later, depending on how much of a health threat the flu poses this fall, the officials said.

FOX News' Jennifer Griffin, Brian Wilson and The Associated Press contributed to this report.

Concerns Surround H1N1 Vaccine Which May Contain Thimerosal

A swine flu vaccine expected this fall is raising red flags because it will likely contain a preservative some link to autism despite scientific research repeatedly proving otherwise.

Government officials say they hope to have 160 million doses of a vaccine for swine flu, or H1N1, available by the fall when flu season is expected to kick in. A vaccine is currently going through clinical trials. Pregnant women, children and health care workers will be the first to be vaccinated.

Scientists say the swine flu vaccine will be similar to the flu vaccines provided annually with little fanfare. However, some consumer groups are reserved about the new vaccine because of the possibility that it could contain thimerosal in combination with a second additive in an effort to produce large quantities more quickly.

Furthermore, a vaccine offered to combat a different strain of the swine flu in the 1970s is linked to increased incidents of a neurological disorder.

But makers of the vaccine say they anticiptate manufacturing two versions, one with and one without thimerosal, which ought to ease some fears, reports ABC News. To read more click here.


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