Upcoming events
  • No upcoming events available
Syndicate
Syndicate content
Current Users
There are currently 2 users and 1 guest online.

Online users

  • anna
  • seoduoduo
Events
« March 2011 »
SunMonTueWedThuFriSat
12345
6789101112
13141516171819
20212223242526
2728293031
Immunization of children does more harm than good
Posted Monday September 14, 2009 at 11:41 pm by Bob Dwyer (district 4)

"There is a great deal of evidence to prove that immunization of children does more harm than good."---Dr. J. Anthony Morris, former Chief Vaccine Control Officer and research virologist, US FDA.

He informed America, on Phil Donahue’s show, that he had been responsible for the testing of the Swine flu vaccine; that it could cause serious allergic and neurological reactions; had a very low potency, and was completely unnecessary as the virus concerned was an ordinary pig virus, and not highly pathogenic, and had died out within two weeks of it’s being detected in February, and had not been seen anywhere else. [2009 Sept] Dear Dr Friedlander (re Dr J. Anthony Morris)

"There is no evidence that any influenza vaccine thus far developed is effective in preventing or mitigating any attack of influenza. The producers of these vaccines know that they are worthless, but they go on selling them, anyway."------Dr. J. Anthony Morris (formerly Chief Vaccine Control Officer at the FDA)

In what is now known as "the Great Swine Flu Massacre," the President of the United States, Gerald Ford, was enlisted to persuade the public to undergo a national vaccination campaign. The moving force behind the scheme was a $135 million windfall profit for the major drug manufacturers. They had a "swine flu" vaccine which suspicious pig raisers had refused to touch, fearful it might wipe out their crop. The manufacturers had only tried to get $80 million from the swine breeders; balked in this sale, they turned to the other market, humans. The impetus for the national swine flu vaccine came directly from the Disease Control Center in Atlanta, Georgia

The fact that there was not a single known case of this flu in the United States did not deter the Medical Monopoly from their scheme. The swine breeders had been shocked by the demonstrations of the vaccine on a few pigs, which had collapsed and died.

Dr. Anthony Morris, formerly of HEW and then active as director of the Virus Bureau of the Food and Drug Administration, declared that there could be no authentic swine flu vaccine, because there had never seen any cases of swine flu on which they could test it. Dr. Morris then went public with his statement that "at no point were the swine flu vaccines effective." He was promptly fired, but the damage had been done. The damage control consisted of that great humanitarian, Walter Cronkite, and the President of the United States, combining their forces to come to the rescue of the Medical Monopoly. Walter Cronkite had President Ford appear on his news program to urge the American people to submit to the inoculation with the swine flu vaccine.

CBS then or later could never find any reason to air any analysis or scientific critique of the swine flu vaccine, which was identified as containing many toxic poisons, including alien viral protein panicles, formal­dehyde, thimerosal (a derivative of poisonous mer­cury), polysorbate and some eighty other substances.

On April I5, 1976, Congress passed Public Law 94-266, which provided $135 million of taxpayers' funds to pay for a national swine flu inoculation campaign. HEW was to distribute the vaccine to state and local health agencies on a national basis for inoculation, at no charge. Hardly had the swine flu campaign been completed than the reports of the casualties began to pour in. Within a few months, claims totalling $1.3 billion had been filed by victims who had suffered paralysis from the swine flu vaccine.

On June 11 the World Health Organization (WHO) raised its swine flu pandemic alert from a 5 to a 6. Phase 6 is the highest level alert, and reflects the speed with which a virus is spreading -- not its severity.

This classification also allows for a vaccine to qualify for a “fast-track” procedure for licensing and approval, and this process is now ongoing for the swine flu vaccine.

What you may not know, however, is that WHO, together with health officials, regulatory authorities and vaccine manufacturers, have been working since 2007 – long before this new “threat” of swine flu emerged – to “explore a broad range of issues surrounding the regulatory approval of pandemic vaccines.”

According to the WHO website:

“Ways were sought to shorten the time between the emergence of a pandemic virus and the availability of safe and effective vaccines.”

One such method used in Europe is to conduct advance studies using a “mock-up” vaccine that contains an active ingredient for an influenza virus that has not circulated recently in human populations.

When testing these mock-up vaccines, it is very possible to release the novel influenza virus into the population, as its purpose is to “mimic the novelty of a pandemic virus” and “greatly expedite regulatory approval.”

Government officials have other tricks up their sleeves to ensure these new, barely tested vaccines easily make it to market as well, such as:

· Labeling the vaccine a “strain change” rather than an entirely “new” vaccine. This method states the new vaccine has built on technology used to produce vaccines for seasonal influenza, and the change for the pandemic vaccine is similar to a strain change used to produce a new seasonal vaccine each flu season.

In the United States, vaccine manufacturers are required to submit fewer data if they already have a licensed flu vaccine and will use the same manufacturing process for the pandemic vaccine.

· Using a “rolling review procedure.” This allows manufacturers to submit sets of data for regulatory review “as they become available.” In other words, they’re free to distribute the vaccine and then submit the safety data later on.

Now, German lung specialist Wolfgang Wodarg has come out about even more potential health risks associated with the swine flu vaccine. Interestingly, Dr. Wodarg also holds political office, as the chairman of the health committee in the German parliament and European Council.

According to Dr. Wodarg, the swine flu vaccine contains animal cancer cells, and there’s no data indicating whether or not this may cause an allergic reaction when injected.

It also raises questions about the risk of contracting cancer.

He also told the German press that the widespread fear of the pandemic was an “orchestration,” stating,

It is great business for the pharmaceutical industry. Swine flu is not very different from normal flu. On the contrary, if you look at the number of cases it is nothing compared to a normal flu outbreak.”

Vaccines contain either killed viruses or bacteria, germ components, toxic extracts or live organisms that have been made less virulent--a process called attenuation. To stimulate an enhanced immune reaction against these organisms, manufacturers added powerful immune-stimulating substances such as squalene, aluminum, lipopolysacchride, etc. These are called immune adjuvants.

Because more and more reports are appearing citing vaccine failure, their manufacturers’ answer is to make the vaccines more potent. They do this by making the immune adjuvants more powerful or adding more of them.

The Baxter swine flu vaccine, called Celvapan, uses cultured cells from the African green monkey, which has previously been implicated as having transmitted a number of vaccine-contaminating viruses, including the HIV virus.

Vaccines typically contain many of the following fillers:

*         aluminum hydroxide

*         aluminum phosphate

*         ammonium sulfate

*         amphotericin B

*         animal tissues: pig blood, horse blood, rabbit brain,

*         dog kidney, monkey kidney,

*         chick embryo, chicken egg, duck egg

*         calf (bovine) serum

*         betapropiolactone

*         fetal bovine serum

*         formaldehyde

*         formalin

*         gelatin

*         glycerol

*         human diploid cells (originating from human aborted fetal tissue)

*         hydrolized gelatin

*         mercury thimerosol (thimerosal, Merthiolate(r))

*         monosodium glutamate (MSG)

*         neomycin

*         neomycin sulfate

*         phenol red indicator

*         phenoxyethanol (antifreeze)

*         potassium diphosphate

*         potassium monophosphate

*         polymyxin B

*         polysorbate 20

*         polysorbate 80

*         porcine (pig) pancreatic hydrolysate of casein

*         residual MRC5 proteins

*         sorbitol

*         tri(n)butylphosphate,

*         VERO cells, a continuous line of monkey kidney cells, and

*         washed sheep red blood

The U.S. government has contracts with several drug companies to develop and produce swine flu vaccines. At least two of those companies are using an adjuvant Squalene in their H1N1 vaccines.

According to Meryl Nass, M.D., an authority on the anthrax vaccine,

“A novel feature of the two H1N1 vaccines being developed by companies Novartis and GlaxoSmithKline 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.”[v]

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

Gulf War veterans with Gulf War Syndrome (GWS) received anthrax vaccines which contained squalene and has since been linked to the devastating autoimmune diseases suffered by countless Gulf War vets.

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

“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.”

There is virtually no science to support the safety of vaccine injections on your long-term health or the health of your children. Follow-up studies last on average about two weeks, and look only for glaring injuries and illnesses.

Autoimmune disorders like those seen in Gulf War Syndrome frequently take years to diagnose due to the vagueness of early symptoms. Complaints like headaches, fatigue and chronic aches and pains are symptoms of many different illnesses and diseases.

Take care of your health, honor your body. Health means Freedom.