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In a message dated 8/3/01 6:58:28 AM Pacific Daylight Time, DSNurse@...

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<< The 1990 Workshop on Pertussis Vaccination

In 1990, a Workshop on Neurologic Complications of Pertussis and Pertussis

Vaccination was convened. It concluded that pertussis vaccines are not

standardized between manufacturers, that vaccines are not standardized by

each manufacturer from one batch to another, that there is no inherent

difficulty in assigning cause and effect to the vaccine and subsequent

permanent neurological damage, that there was sufficient experimental data

to

implicate both endotoxin and pertussis toxin in adverse neurological

reactions to pertussis vaccine, and that there was a consensus between

neurologists that the seizures following pertussis vaccination could not

accurately be described as " febrile convulsions " because they are not

necessarily benign. Incredibly, in the face of their own conclusions, they

released a report that concluded " there is no demonstrated association

between DPT vaccination and SIDS, because sudden death after pertussis

vaccination is too rare to be detectable in the context of presently

available series. " There are 10,000 cases of SIDS in the United States each

year. The conspiracy runs deep. In the 1990 Journal of the American Medical

Association an editorital clearly labelled vaccine-induced encephalopathy " a

myth " , ironically accusing the American Association of Pediatrics (AAP) " and

other well-meaning physicians " of " joining forces with parents groups and

lawyers. " Ironic, because the AAP was the one who recommended in 1992 that

babies in the United States should be given five doses of pertussis vaccine.

It is interesting how the AAP changed their tune within two years. The end

result of this insanity led to the formation of the National Vaccine Injury

Program.

Another bit of irony is that finally in 1992, the Institute of Medicine

admitted that " the evidence is consistent with a causal relation between DPT

vaccine and acute encephalopathy, defined in the studies reviewed as

encephalopathy, encephalitis or encephalomyelitis, and the evidence

indicates

a causal relation between DPT vaccine and anaphylaxis, between the pertussis

component of DPT vaccine and protracted, inconsolable crying. " In other

words, brain damage in progress.

Harvard Medical School and Federal Drug Administration Tests on DPT Vaccine

Almost 50 years ago in 1948 two Harvard Medical School scientists, Randolph

Byers and Frederick Moll, carried out tests on DPT vaccines at Children's

Hospital in Boston and concluded that severe neurological problems followed

administration of DPT vaccines. The results of the tests were published in

Pediatrics, a respectable medical journal. They were ignored by the medical

and pharmaceutical community, who had a vested financial interest in

continuing the practice. In 1976, Manclark, an FDA scientist,

remarked that " the DPT vaccine had one of the worst failure rates of any

product submitted to the Division of Biologics for testing. "

DPT Trivalent Vaccine Composition and Physiological Action

Approximately 3.3 million children are injected each year with DPT vaccine,

which is composed of the toxoids of diphtheria and tetanus, along with whole

cells of pertussis bacteria. Again, toxoids are defined as the toxins

emitted

by organisms when they grow in a culture. Tetanus toxins are produced in

culture consisting of beef heart infusion, containing by nature animal

bacteria, viruses and antigens foreign to the human body, as well as

dextrose

(sugar), sodium chloride (salt) and casein (a bovine milk by-product).

Diphtheria toxoids are produced in a similar manner. They used to be

produced

from antibodies gained from blood of horses injected with diphtheria

bacteria. After it has been determined that a sufficient amount of toxic

by-products have been produced, the cultures are filtered to obtain a

reasonably clear solution containing the toxic cellular by-products of the

bacteria, plus animal viruses and foreign protein antigens. Formalin is

added

to cause any particles left to clump. Formalin is a derivative of

formaldehyde (a carcinogen used to embalm bodies). Wood alcohol, methanol

(toxic) is added to cause the toxoid particles to precipitate into a fine

powder. Whole cells of deadly pertussis bacteria that have been killed by

thimerosal ( also known as merthiolate), a mercury compound, are added to

the

mixture. Over 35mg of thimerosal will kill a rabbit. Thimerosal also

destroys

the " potency " of the vaccine, affects growth patterns of human cells it

comes

into contact with, and inhibits the action of human white blood cells,

inhibiting the process of phagocytosis. Thimersol is five times more toxic

to

human cells than it is for Staphlococcus bacteriaand, as a mercury compound,

produces an allergic reaction in the body.

A substance called an " adjuvant " , which initiates reactionary antibody

formation, is added. Common adjuvants are aluminum hydroxide and aluminum

potassium sulfate. The mixture is then put into vials for injection into

children. In the body, the formalin coating dissolves, releasing all

bacterial and viral particles from animal culture sources. The thimerosal

and

adjuvant chemicals irritate the body tissues and increase the action of

accompanying bacteria and viruses, as well as the reaction of the immune

system to the foreign protein antigens, severely damaging neurological

membranes, especially in babies and children, where the myelin sheath has

only partially protected the nervous system, resulting in mild to severe

neurological damage, production of learning disabilities and other nervous

system disorders, or death, especially upon subsequent injections where the

cellular structure of the body has already been sensitized, promoting

allergic reactions and responses of increasingly severe nature.

Promotion of Disease Processes By Chemicals in Vaccines

Between 1940 and 1955, it was noticed that children who had been recently

injected with pertussis vaccine suffered paralytic polio at an increased

frequency over those who had not received pertussis vaccine. During a polio

outbreak in Minnesota in 1946, eighty-five children came down with polio.

Thirty-three of them had recently received pertussis vaccine five to

nineteen

days earlier, and the limb injected with the pertussis vaccine was paralyzed

in 58% of the children affected. In 1949, the risk of contracting paralytic

polio for infants was four times higher if they received a

diphtheria-pertussis injection within the previous six weeks before exposure

to the virus, as compared to an un-injected group of control infants. In

1953, research on a polio epidemic on some Pacific islands revealed that the

children on the island, who were receiving weekly injections of a solution

of

mercury, arsenic and bismuth to combat an infestation of spirochetes,

experienced polio at ten times the rate of children on the islands not

receiving the treatment.

The 1954 study on " Provoking and Localizing Factors in Poliomyelitis, "

conducted by Trueta and Hodes and published in Lancet, journal of the

British

Medical Association, outlined research performed since 1900 on diverse

factors that appeared to increase the severity of poliomyelitis or localize

it to a specific area in the nervous system. As early as 1920, researchers

were sure that the polio virus migrated through the body by way of the

circulatory system. This bit of research prompted Trueta and Hodes to make

the suggestion that the factors which influence the severity and

localization

of polio might somehow modify the pattern of blood vessels in the nervous

system, increasing the permeability of the blood-brain barrier, giving polio

easier access to both the brain and the nervous system. Experiments with

formalin and other substances illustrated that these type of substances

caused engorgement of blood vessels in areas corresponding to areas of

paralysis. Their research, and subsequent work, has confirmed that some of

the substances such as formalin that are routinely added to vaccines have

the

effect of increasing the severity of disease and the probability of death,

depending on the bacterium or viruses that are injected with these

chemicals.

A subsequent study in 1954 by the Medical Research Council of Great Britain

revealed that diphtheria-pertussis vaccines, especially those precipitated

using aluminum compounds, predisposed children to paralytic polio. In 1957,

the eminent biologist Dubos proved that when pertussis vaccines or killed

mycobacteria were injected into animals infected months earlier with small

doses of bacteria, the subsequently injected bacteria multiplied

explosively.

In other words, pertussis vaccine is able to accelerate latent infections

into active acute infections. Since medical authorities fail to thoroughly

examine people injected with vaccines, they cannot detect latent infections

which can be reactivated by injection of vaccines and accompanying chemical

preservatives and bacteriostatic drugs.

Total Annual DPT Statistics for the United States

DPT vaccines, no matter what the formulation, appear to have a devestating

effect on the neurology of American children. Out of 3.3 million babies,

infants and toddlers injected each year, over 33,000 experience acute

neurological reactions, with 8,500 experiencing convulsions and/or collapse,

and over 16,000 have episodes of high-pitched screaming indicating brain

damage in progress. The general complication rate with DPT vaccine is

estimated to be over 10,000 for every million injected. If 33,000 postmen

shot themselves in the head each year, would there be notice taken of it?

The

fact that the slaughter and injuries have not stopped is due more to lack of

mass awareness of the dimension of the problem.

Efforts at Population Control Using Tetanus Toxin as a r

Leading Edge Research is a member of the National Vaccine Information

Center,

and as such we have access to a continual flow of valuable data and

information concerning activities within the vaccination paradigm. One of

the

more interesting things to arise in 1995 was the revelation that the World

Health Organization (WHO), in concert with the Centers for Disease Control,

the American Academy of Pediatrics, the World Bank, the United Nations, the

Rockefeller Foundation, the Population Council, the U.S. National Institutes

of Health, Great Britain, Sweden, Norway, Denmark, Germany and several

universities, including those at Helsinki, Uppsala and Ohio State

University,

have been working for nearly 25 years on an anti-fertility vaccine using hCG

(human chorionic gonadotrophin) tied to a tetanus toxoid vaccine. Two

decades

of medical journals have detailed their progress. By injecting a woman with

hCG, using tetanus toxoid as a carrier, the woman's immune system not only

produces antibodies against tetanus, but also produces anti-bodies against

hCG. When the woman subsequently becomes pregnant, the hCG antibodies will

cause her to abort her baby because there will be too little hCG (normally

needed to maintain a pregnancy) in her body.

In June 1995, Human Life International, a large human rights and pro-life

organization, raised questions about the program, as well as the apparent

activity of the WHO, where millions of unsuspecting women in Mexico, the

Philippines and Nicaragua are being used as human guinea pigs in which they

are injected with an anti-fertility vaccine but are told it was nothing more

than a tetanus vaccine. After becoming suspicious of protocols in what the

WHO billed as " a massive campaign to reduce the incidence of neo-natal

tetanus " , pro-life groups in the Philippines had vials of the vaccine

independently tested and discovered that they contained hCG.

According to , who reported on the controversy in the June 1995

HLI Reports newsletter, when the first reports surfaced in the ines,

health officials at the WHO and ine health agencies categorically

denied the vaccine contained hCG. When confronted with lab test evidence

showing the vaccine vials contained hCG as well as laboratory evidence that

there were high levels of hCG antibodies in 27 out of 30 women who had been

vaccinated, WHO officials started to make excuses. Now, why would they try

to

hide the fact that hCG was in the vaccine unless they knew they were doing

something unethical?

According to , " first they said there was no hCG in the vaccine , then

they said there was, but it was in tiny amounts. Then, they said that hCG is

part of the vaccine manufacturing process. Now, they are saying the tests to

detect hCG are flawed and produce 'a lot of false positives'. But, there is

one fact that cannot be disputed. There is no known way for the vaccinated

women to have hCG antibodies in their blood unless hCG had been artificially

introduced into their bodies. "

Tetanus vaccine has historically been given to individuals every ten years

as

standard allopathic practice, despite the criminal nature of the procedure.

Tetanus vaccine is usually given allopathically in the event of a severe

injury. Evidence that vaccinating pregnant mothers " to prevent neo-natal

tetanus " is illogical, anecdotal, and is not supported but any evidence

whatsoever. It is interesting that the CDC is also recommending that

pregnant

mothers also receive AZT " to prevent transmission of HIV to babies " and that

newborn babies receive AZT. Of course, AZT is an experimental chemotherapy

chemical which is lethal to all cellular structures. Both instances

constitute willful criminal negligence tantamount to genocide, both for

mothers and babies.

According to the CDC, who has been promoting elimination of neonatal tetanus

in the Third World, " hundreds of thousands of infants die from neonatal

tetanus in mostly underdeveloped countries every year because they are born

in unsanitary conditions and their umbilical cords become infected with

tetanus bacteria. " CDC protocols discuss " the need " for pregnant women to

receive two injections of tetanus vaccine. The WHO tetanus campaign in the

Philippines, Nicaragua and Mexico (afta NAFTA?) targeted " all women of

childbearing age and adult women " and injected with with three doses of

vaccine within 90 days, following up with two more doses for a total of five

tetanus shots. One Roman Catholic nun was quoted as saying that health

officials " started vaccinating teenagers without their consent and were even

going house to house. " Human Life International is calling for a

Congressional investigation, which NVIC endorses, to explore human rights

abuses connected with the mass vaccination campaign.

Human Life International, as they indicated in HLI Reports (Vol 13 No.6 June

1995) placed an exploratory call to the Montgomery County (land) Health

Department, Epidemiological Division, Infectious Diseases and Adult

Immunizations to inquire about the frequency of tetanus vaccinations. The

answers provided by the Health Department were revealing:

Q: For how long a time does the tetanus vaccine " offer protection " ?

A: 10 years.

Q: Have you ever heard of any adult requiring three tetanus vaccinations

within

a 3 or 4 month time period, and a total of five vaccinations in all within a

year or so?

A: Whaaat! Never. No way!

So, even " standard allopathy " doesn't agree with the protocol that is being

implemented by the WHO, in concert with the rest of the " anti-fertility

gang. "

>>