Leading Edge Master Analysis of the Vaccination Paradigm

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, Charles 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 Carrier

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 James Miller, who reported on the controversy in the June 1995 HLI Reports newsletter, when the first reports surfaced in the Phillipines, health officials at the WHO and Phillipine 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 Miller, "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 (Maryland) 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."