Are Parents Being Manipulated?
30 Tactics Used by the Medical Profession
to Hoodwink the Public
Medical health authorities, including doctors, nurses, and other members of the allopathic fraternity, employ a number of strategies designed to elicit parental submission to vaccine guidelines. Currently, parents are expected to grant authorities permission to toxify their children’s pure and sacred little bodies with more than 30 blends of rare germs, bacteria, and other foul substances — all before they enter school!
To adequately assess the relevance of vaccine-related news, or the perils of vaccine-related situations you may find yourself in — and to increase your knowledge about how to protect your loved ones — several of the more common vaccine-related schemes you’re likely to encounter are included in the following section, along with samples of each.
1. Calling the Shots “Immunizations.” Numerous studies indicate that vaccines cannot be relied upon to boost the immune system and protect an individual from contracting the disease the vaccines were designed to offset. For example, the Minnesota Department of Health reported 769 cases of mumps in school children. But 632 of these cases (82 percent) occurred in children who were previously vaccinated against this disease.(119) The Centers for Disease Control and Prevention (CDC) reported that 89 percent of all school-age children who recently contracted measles had been vaccinated against the disease.(120-122) And the New England Journal of Medicine published a study revealing that the pertussis vaccine “failed to give…protection against the disease.” In fact, more than 80 percent of cases in a recent epidemic occurred in children who had received regular doses of the shot.(123,124)
According to Dr. Sandra Huffman, head of Nurture: The Center to Prevent Childhood Malnutrition, “Increasing Americans’ breastfeeding rate would prevent more childhood diseases — and deaths — than [vaccination programs endorsed by the government].”(125) A distinction must therefore be made: breastfed babies are immunized;(126-128) children who are injected with germs and other toxic substances are vaccinated.
Calling the shots “preventive medicine” is deceptive as well. According to Dr. Kenneth Cooper, pioneering author of Aerobics, “My concept of preventive medicine is trying to prevent the things that kill us. Infectious disease is way down the list.”(129) (Dr. Cooper was ostracized from the medical community for promoting exercise to improve health!)
2. Rationalization and Denial. Medical personnel find it difficult to confront the vaccine issue head-on. It is much easier to falsely justify the use of vaccines or simply reject the idea that they may be unsafe and ineffective. Some doctors become so agitated when the topic is raised, they refuse to even discuss it. Doctors who are willing to exchange ideas and concerns regarding the safety and efficacy of vaccines often rely upon rationalization and denial.
The rationalization and denial ploy can be blatant or veiled. Blatant rationalization is easier to spot. For example, in a recently published pediatric legal paper, a Canadian neurologist candidly writes, “In this article [on vaccine-induced brain injury], I will…offer some suggestions for pediatricians to rationalize this emotional controversy.” He also plainly states, “A vigorous effort is required to dispel the myth of DTP-induced brain damage.”(130) He makes his recommendation in spite of the horrendous amount of literature in the medical journals indicating a causal relationship between this vaccine and severe mental impairment.(131)
The veiled Rationalization and Denial ploy is harder to detect. At first it appears logical and sound. But it merely represents a more intricate attempt at suppressing and confounding the truth. For example, according to some researchers, the DPT vaccine does not cause seizures; instead, “fever from the DTP vaccine may trigger one of these seizures.”(132) Or, according to an experienced vaccine policymaker, Ed Mortimer, M.D., “These kids already had underlying problems and DTP was the first fever-producing insult that occurred to the child.”(133) Again, it wasn’t the vaccine that caused the brain damage; it was the fever from the vaccine.
More examples of the rationalization and denial ploy:
When the incidence of a disease is low, authorities claim high vaccination rates are responsible. When outbreaks occur, we are told not enough people received the shots. For example, prior to a recent measles outbreak in a Hobbs, New Mexico, school district, authorities boasted a 98 percent vaccination rate. Then, when 76 cases of the disease broke out, researchers claimed that “vaccine failure was associated with immunizations that could not be documented in the provider’s records.”(134)
Although the Food and Drug Administration was legally bound to establish and oversee the Vaccine Adverse Event Reporting System (VAERS), and even though every year about 12,000 reports of adverse reactions to vaccines are made to the FDA,(135) authorities refuse to follow up on these cases because “the agency could not possibly investigate each report,” and besides, “a cause and effect relationship is not presumed.”(136)
By November 10, 1999, the Vaccine Injury Compensation System had already paid out more than $1 billion to settle claims of vaccine-induced damage or death.(137) However, because vaccine manufacturers and the federal government are not required to admit responsibility, even when a claim is paid, they are able to assert that “the settlement of a claim does not necessarily establish liability.”(138)
3. Double Talk and Creative Logic. Medical advisers were using this ploy as far back as 1806. In that year Edward Jenner, the dubious “father of modern vaccinations,” was under examination by a College of Physicians committee. Numerous members of the English population who had recently been vaccinated with Jenner’s concoction, and who were therefore considered immune to smallpox, had caught the disease. Many were afflicted with painful skin eruptions and died. When the commonly relied upon denial ploy was no longer effective, it was revealed that “spurious,” or phony, cowpox was the cause. As the number of vaccinated people afflicted with the disease grew, so, too, did public fear. How, Jenner was asked, could spurious cowpox be identified and avoided? Spurious cowpox, he explained, wasn’t meant to describe irregularities on the part of the cow, but rather certain quirks in the action of cowpox on the part of the vaccinated. In other words, when the vaccinated recovered from the ordeal, and did not contract smallpox, the cowpox was genuine; otherwise it was spurious.(139)
Current uses of the double talk ploy may be found at almost any forum or seminar where vaccine policymakers congregate. For example, at a recent FDA workshop officials indicated they were justified in administering new and unproven vaccines by claiming it is unethical to withhold them!(140)
Here is another example of the “unethical” argument: A recent study found that the AIDS virus directly causes cancer. You’d think this would stifle the researchers’ goal of creating an AIDS vaccine. In fact, Gerald Myers, director of the HIV Sequence Database Analysis Project at Los Alamos National Laboratory, warrants that a live vaccine would carry a risk of causing cancer — both in the vaccinated person and in their offspring. Nevertheless, he claims that “the risk might be worth it” to prevent the spread of AIDS. “It could be unethical not to try it.”(141)
A common use of the double talk and creative logic ploy may be found whenever health officials make the outrageous claim that unvaccinated children are a threat to the rest of society. This argument indicates how little faith authorities place in their own vaccines. If the vaccines were truly effective, only the unvaccinated would be at risk. This argument also overlooks the potential for vaccinated individuals to spread the virus to unvaccinated populations. For example, in separate scientific studies, the new rubella vaccine introduced in 1979 was found to be a cause of Chronic Fatigue Syndrome, an immunological disorder first reported in the United States in 1982. Given to children, the vaccine was shown to linger in their systems for years and the vaccine virus can be passed on to adults through casual contact.(142-144)
In an attempt to conceal vaccine failures, medical authorities will often resort to the double talk ploy, sometimes in conjunction with the scare tactics ruse. In spite of their enterprising babble, however, they can’t always hoodwink the public. For example, the international Medical Observer states that “a new strain of measles resistant to vaccine” has been discovered. This is immediately contradicted by the statement: “Those who have been lax about vaccination will be unprotected.” Although the implication is that everyone should get vaccinated, a vaccine is obviously useless if a new strain of measles is resistant to it!(145)
More examples of the double talk ploy:
Scientists seeking human volunteers to test a new experimental AIDS vaccine try to assuage fear and mistrust by claiming there is “no evidence” it will cause AIDS. How could there be evidence? It is new and experimental and hasn’t been tested yet! And, of course, there is “no evidence” that it won’t cause AIDS.(146)
In an attempt to convince the public that vaccines offer the best of all worlds, medical researchers, and the journalists who quote them, often get tangled in their own webs of deception. For example, in a recently published pro-vaccine article, the author claims that unvaccinated children are susceptible to infection. He then contradicts himself by claiming that vaccinated children “insulate” or protect, the unvaccinated. The illogical implication is that when unvaccinated children contract an infectious disease it is because they are unvaccinated. However, if they remain free from disease, it is because the vaccinated are providing them with immunity.(147)
Every so often the double talk employed by authorities is so transparent it’s bewildering that so few people question its validity. In a recent promotional blitz, flu vaccine manufacturers and public health officials made the claim that the new and improved flu vaccine “is prepared from inactivated flu virus [Translation: “dead” flu virus — see Euphemisms addressed below] and cannot cause the disease.” (A rare admission that earlier versions did cause the disease.) In the same paragraph they warn that “some individuals might develop a mild fever and feeling of malaise” for a few days after receiving the shot.(148) (Sounds like the flu to me!)
Other times the double talk employed by vaccine researchers is remarkably elaborate. Although it is a simple matter to determine the efficacy of a vaccine — give it to people who want it, withhold it from those who don’t, and tally the incidence of disease — some scientists have other ideas. One writes: “Under heterogeneity of vaccine effect, a general expression for a summary vaccine efficacy parameter is a function of the vaccine efficacy in the different vaccinated strata weighted by the fraction of the vaccinated subpopulations in each stratum. Interpretation and estimability of the summary vaccine efficacy parameter depends on whether the strata are identifiable, and whether the heterogeneity is host- or vaccine-related.” To support this garrulous babble, a full-page mathematical model is provided.(149)
A final look at the double talk and creative logic ploy yields the following revelations: children who keep to “appropriate” vaccine schedules are “protected,” unless they haven’t yet received the full battery of shots and contract the affliction — in which case they are evidently “still susceptible to the disease.”(150) In such instances the vaccine does not fail, or worse, cause the disease; these become “non-preventable” cases!(151)
4. The “I Forgot to Mention” ploy is a common tactic used by health and medical authorities with an interest in omitting vital information. For example, a spokesman for the Ohio Department of Health supplied the Dayton Daily News with these statistics: 2,720 cases of measles were reported in Ohio during a recent year. This figure was used in conjunction with the godfather ploy (an offer hard to refuse) when the following threat was made as well: “Get shots or forget 7th grade.” What the official failed to mention was that more than 72 percent of these cases occurred in vaccinated people.(152) This figure is comparable to other outbreaks around the country, where a majority of measles cases often occur in vaccinated children, “sometimes in schools with vaccination levels of greater than 98 percent.”(153,154)
A concerned individual recounts her personal experience with the measles vaccine and the “I forgot to mention” ploy: “Fort Lewis College had a measles epidemic and the school closed down for a short time. The following year, I returned as a postgraduate for a teacher’s certificate and was denied reentry until I submitted to a measles vaccine — even though I had been fully vaccinated as a child. This fall I reentered Fort Lewis College, and they wanted me to get another measles shot! They told me the one I had already taken ‘didn’t work.’ I refused the shot and told them I was refusing all other shots as well. They replied, ‘Okay, just sign this waiver.’ No one ever tells you that the shots may be declined by signing a personal waiver.”(155)
Another example of the “I forgot to mention” ploy may be found in official evaluations of Reye’s Syndrome, an often fatal disease of the brain and liver. According to Dr. Robert Mendelsohn, the CDC is “quick to suggest a relationship between [this childhood disease] and certain flu outbreaks,” but they make no mention of “an association between this disease and the flu vaccine itself.”(156)
5. Gimmicks. Devising strategies to boost vaccination rates is a prime preoccupation of vaccine policymakers. Without doubt, the gimmick ploy is a proven winner. In fact, the AMA recently admitted that “adult vaccines need a gimmick.”(157) CDC physicians recommend catchy slogans, like “Vaccines are not just kid stuff.”(158) Shari Lewis and her puppet, Lamb Chop, were seen delivering pro-vaccination messages to the public on TV.(159) Even Bill Clinton was seen in print ads imploring parents to be sure their children receive “All their shots while they’re tots.”(160)
6. Bribes. Within the same family of wily maneuvers, one may find the bribe ploy. For example, in England the National Health Service pays a “bonus” to doctors with vaccination rates above specified percentages.(161) Here in the United States, former president Jimmy Carter was seen on TV offering free Michael Jackson concert tickets to parents who agreed to vaccinate their children.(162) In Saginaw County, Michigan, children were promised “a free order of french fries” if they were one of the first thousand people to receive their shots.(163) And in Taos, New Mexico, “all students who return consent forms and receive vaccinations will be entered in raffles for great prizes!”(164)
7. Skewed Statistics. Researchers are trying to develop a new vaccine to combat respiratory syncytial virus (RSV) — even though Dr. Bill Gary of the Centers for Disease Control and Prevention (CDC) admits that “an RSV vaccine was developed 10 to 15 years ago, but was unsuccessful and made many people ill.” To foster interest in this obscure project, and to improve the illusion that we need the vaccine, a recent report released by the CDC indicates that “about half” of the 69 labs that track diseases for the agency reported a 16 percent increase in RSV cases.(165) Stating “about half” is deceptively vague, and choosing not to list the percent increase or decrease of RSV cases in the other “about half” of the 69 labs is manipulative and dishonest.
Another good example of the skewed statistics ploy came from the Clinton administration. Goaded by the medical community, federal authorities announced their dubious goal to vaccinate all U.S. children. To accomplish this feat, Clinton sought $300 million from Congress. To bolster his case he made the bogus claim that “we can prevent the worst infectious diseases of children with vaccines and save $10 for every $1 invested.”(166) But he failed to supply facts and figures to support his claim. Perhaps this was because the administration chose instead to invoke the “I forgot to mention” ploy, conveniently neglecting to factor in the millions of dollars the government had already spent compensating families of children damaged or killed by the vaccines.(167)
A further example of the skewed statistics ploy:
The use of control subjects (individuals utilized as a standard of comparison for verifying the results of an experiment) is an established procedure in most fields of scientific inquiry. Not so within the vaccine research community. New experimental vaccines that are tested on a group of people are rarely matched against an equal number of untested people. Indeed, after a new AIDS vaccine was tested on hundreds of people, some of the volunteers were found to be infected with HIV. However, because the number of control subjects was suspiciously small (38 people) — and therefore worthless — the National Institutes of Health (NIH) was able to claim “there is no statistical basis for concluding that the vaccine has contributed to an increased vulnerability to infection.”(168)
8. The Fraud ploy has proven to be an early and consistent success. In 1956, soon after the Salk polio vaccine was introduced, officials decided to determine how safe and effective it really was. The results of this study — the now infamous Francis Field Trials — would help determine the feasibility of continuing to vaccinate millions of young children. What they discovered would have stopped most ethical people from continuing: large numbers of children were contracting polio after receiving the vaccine. Clearly, the vaccine was either unsafe (it was causing the disease it was meant to prevent) or ineffective (it failed to protect). Instead of removing the vaccine from the market, however, officials decided to exclude from the statistics all cases of polio that occurred within 30 days after vaccination on the pretext that such cases were “pre-existing.”(169,170)
The NIH, an influential branch of the vaccine oligarchy, was recently placed under investigation for interfering with charges of scientific fraud within its own ranks. According to a New York Times report, Walter W. Stewart and Dr. Ned Feder, scientific fraud investigators for the NIH, were summarily dismissed from their duties following the release of a report critical of other NIH scientists. Without warning their offices were closed and sealed, along with all the files of current investigations. The two scientists were then transferred to jobs unrelated to their work of previous years. This incident reveals how studies and reports critical of official dogma may be suppressed, and highlights “the continuing ethical battles over how government and universities should monitor scientists.”(171)
9. Fortune-telling. When medical and health authorities are at a loss to explain the cause of injury and death that occurs soon after a childhood shot, and denial is insufficient, they may resort to the fortune-telling ploy. In fact, the FDA’s official position is that “the ‘event’ [Translation: adverse reaction to a vaccine — see the Euphemism ploy] may have been related to an underlying disease or condition…or may have occurred by chance at the same time the vaccine was administered.” In other words, the child was destined to be damaged or die at the time of the shot anyway.(172)
The past director of the Ohio Department of Health, and other vaccine authorities, label vaccine-induced injury or death as “only temporal.: Once again, this translates to mean the damage was coincidental; it would have occurred anyway.(173)
More examples of the fortune-telling ploy:
“Bad Flu Season Forecast” blared the headlines. “A severe flu season is at hand; get flu shots right away.”(174) Who are these doomsday prophets, and where do they get their psychic news?
According to the U.S. government’s Morbidity and Mortality Weekly Report (MMWR), the efficacy of a flu vaccine depends upon whether the government has correctly “predicted” [Translation: guessed] which viruses should be placed in that year’s vaccine. There has to be a “good match” between the flu virus actually present in the community at the end of the year and the vaccine that was produced several months earlier.(175)
10. “Pardon Me.” Medical institutions wary of vaccine reactions often protect their members by enforcing the “pardon me” rule, exempting doctors from their own regulations. For example, in Evanston, Illinois, a 46-year-old social worker was fired from her job when she refused to take a rubella shot. Hospital policy requires all employees —except physicians — to be vaccinated against rubella. Doctors are not considered “employees.”(176)
A study published in the Journal of the American Medical Association reports that obstetrician-gynecologists are the least likely of all doctors to submit to the rubella vaccine. Fewer than 10 percent are inoculated, and blood tests indicate they are susceptible to rubella. The researchers conclude that a “fear of unforeseen vaccine reactions” lead these specialists to invoke their self-exempting “pardon me” rule.(177)
Some doctors refuse to vaccinate their own children as well. According to Dr. Jerome Murphy, former head of Pediatric Neurology at Milwaukee Children’s Hospital, “There is just overwhelming data that there’s an association [between the pertussis vaccine and seizures]. I know it has influenced many pediatric neurologists not to have their own children immunized with pertussis.”(178)
The FDA recently lost an important legal battle when they permitted the live virus polio vaccine, manufactured by Lederle Labs, to be released to the public even though it did not meet existing safety standards. As a result, several people were severely damaged. After losing the U.S. Supreme Court case, the FDA immediately implemented the “pardon me” ploy, and rewrote its safety procedures so that previously unacceptable safety measures would be allowable. Consequently, Lederle can continue to produce and the FDA can continue to sanction the same kind of polio vaccine that caused injuries in the first place.(179)
11. Delusions of Grandeur. Doctors, medical scientists, allopathic policymakers, and vaccine manufacturers, are prone to experience delusions of grandeur. This occurs whenever they take credit for a drop in nearly every communicable disease. But a greater than 95 percent decline in the incidence and severity of many of these diseases already occurred before the introduction of the vaccines. Such conceit also disregards the many diseases — like scarlet fever and the plague — that declined on their own, even though vaccines were not developed against them.(180)
Health officials claim high vaccination rates are required to disrupt the spread of a disease and eliminate its occurrence. For example, they take full credit — delusions of grandeur — for the current low incidence of polio in the United States. However, in many European countries that refused to mandate polio vaccines a fraction of the people were vaccinated, and polio disappeared.181 To explain this enigma, officials rely upon the double talk and creative logic ploy: evidently enough people were vaccinated “to interrupt the virus’s normal lines of transmission through the population.” Yet, countries like Finland used the killed-virus vaccine, which officials do not credit with the ability to confer immunity upon the unvaccinated!(182)
More recently, Finland has claimed to have “eradicated” measles, mumps, and rubella — even though only 30 percent of the people were vaccinated. Also, although researchers claim these diseases were “eradicated,” they note that there are about “ten cases of each disease a year, most of them ‘probably imported’ [from another country].”(183)
Vaccine policymakers promised that by 1982 measles would be eradicated from the Earth�delusions of grandeur.184 Today, in the 1990s, it has returned with a vengeance. The death rate for measles is more than 20 times higher than before the vaccine was in widespread use.(185)
Medical policymakers are unrelenting in their efforts to play God. After realizing “the number of visits to a healthcare provider [for vaccines] is an impediment” to receiving the entire battery of shots, they proposed the development of a single vaccine to provide “lifelong immunization” against many common childhood diseases. They call this single shot a “supervaccine” or “magic bullet” and have lobbied Congress for funds to continue research along these lines.(186) When we consider the medical community’s inability to provide lifelong immunity against a single disease, their dismal success rate with current multiple vaccines (DPT and MMR), and the number of vaccine-related injury and death claims clogging the courts, this latest “mad science” venture clearly demonstrates their wicked propensity toward delusions of grandeur.
12. Surprise Attack. Parents often report they are harassed by medical personnel wishing to vaccinate their children even when they visit their medical health care provider for other reasons. In fact, some doctors appear to be so obsessed with the vaccination status of their clients that they disregard the stated purpose of the visit. Therefore, anticipate the surprise attack.
The surprise attack is actually taught to members of the medical fraternity, as noted in the Journal of the American Medical Association: “Each encounter with a health care provider, including an emergency department visit or hospitalization, is an opportunity to screen immunization status and, if indicated, administer needed vaccines. Before discharge from the hospital, children should receive immunizations for which they are eligible. In addition, children accompanying parents or siblings who are seeking any service should also be screened and, when indicated, given needed vaccines.”(187)
The consequences of being unprepared for the surprise attack can be severe indeed. The Jonathan story published elsewhere on this site illustrates one parent’s reaction to being ambushed by the medical profession.
Another concerned mother describes her surprise attack in these words:
“My husband and I chose a midwife and had a homebirth, which was wonderful. The midwife insisted that I take our daughter to a local pediatrician for a newborn exam…. The reason I’m telling you this is because we were treated like trash. I was told that a homebirth is an automatic ‘red flag.’ The doctor reported us to Social Services, and we were subjected to a painful interrogation. I was [also] interrogated as to my beliefs about immunizations. My daughter was only two weeks old…and yet they wanted to inject her with multiple vaccines.
“How can I find a doctor for my daughter? I do not want to repeat this horrible experience…for fear Social Services will again be sent to investigate us because we don’t take our daughter to doctors for regular ‘well-baby’ checkups, which is really a ploy to force vaccines on innocent babies and unsuspecting parents.”(188)
13. Intimidation and Coercion. Doctors often claim vaccines are mandatory. Many threaten to withhold treatment, or they frighten parents when they reject the shots. As one mother puts it: “The pediatrician I have refused to service me because I am not willing to follow medical ‘rules.’ Another M.D. agreed to work with me, but only after I listened to him warn me [in very explicit terms, about all the dangers that could happen to my child.]”(189)
Another mother writes: “I am a concerned parent who has not vaccinated my 13 month old. I am met by my baby doctor in a critical and almost attacking nature. There seems to be no room in his mind-set for a choice on this issue.”(190)
Putting this in clearer perspective, another mother writes: “I am an Australian citizen [living in the United States]. I never realized what an issue [vaccinations are] in this country until I had my own children, and how much pressure the medical world puts on you, and above all else, how much clout the schools have. I really don’t know of any other country that makes this into such a difficult decision, and so one-sided in regard to information. Where I’m from, you either do, or you don’t, immunize. The question is asked, the decision made, and that’s it forever, unless you change your mind! Incidentally, a large majority [of parents in Australia] do not immunize [their children], and we don’t have a higher incidence [of disease] than in the U.S.”(191)
Note: The United States has one of the worst infant mortality rates among developed countries. In fact, the rate at which babies die in the first year of life has consistently increased since the 1950s when mass immunization campaigns were initiated. Today, infant mortality rates in some U.S. cities match those in developing countries.(192)
Public school officials — the unwitting henchmen for the medical profession — often warn parents their children will not be able to enter school without complying with vaccine mandates. Each state, however, offers one or more exemptions to the shots. In spite of these exemptions, one mother was told by authorities that she would need to write a letter explaining why her son was not vaccinated, and that she would accept full responsibility for any epidemics that occurred while her child was enrolled at the school!(193)
A concerned father tells this story: “I applied for religious exemption for my son at his public school in Totowa, New Jersey. The school nurse reported the exemption to the Board of Health. The New Jersey State Immunization Supervisor then sent a letter to the school principal. In it he stated that my letter of exemption was ‘not good enough,’ and that my son is not to be admitted into the school building at all. The school principal wrote me a letter confirming that my son would not be permitted to enter school, and threatened that `I had better begin immunizing’ my son. I must meet the August deadline to register my son for school, but they won’t even let him in the building. Time is running out, and my son’s education is being denied.”(194)
Note: This story is often told by parents throughout the nation. Evidently, state laws are immaterial to authorities intent upon using the intimidation and coercion ploy to deny parents their legal rights. For example, a clause in the New Jersey State Sanitary Code, Chapter 26:1A-9.1, allows for “exemption for pupils from mandatory immunization if the parent or guardian objects thereto in a written statement signed by the parent or guardian upon the ground that the proposed immunization interferes with the free exercise of the pupil’s religious rights.”
An apprehensive California mother reports that when her child was rushed to the hospital emergency room for a minor mishap, medical personnel were more interested in the child’s vaccination status than in the nature of her injury [the surprise attack]. Upon learning the child was not “up-to-date” on her shots, they refused to release the child to her mother until she gave her permission for the shots to be administered. When she refused, these doctors reported her to Social Services, claiming she was “abusing her child.” Soon thereafter the State Attorney General joined in the case and sought to prosecute the mother —even though the vaccine laws in her state permit parents the option to refuse vaccines based on personal convictions against them!(195)
Many parents report that doctors and nurses are intimidating them into vaccinating their newborns immediately after birth. One mother reports: “The very first time I heard about the hepatitis B vaccine was at the hospital after giving birth to my second child. They told me all babies must receive this vaccine before they can be released from the hospital. Needless to say, I refused it, although they persisted in badgering me. Later, when I took my baby to the pediatrician for her two-week checkup, he tried to frighten me into giving her the shot. He said hepatitis is very contagious and my child could easily catch it from other kids or infected adults. When I told him that I didn’t feel right about giving the vaccine to my infant, he informed me that I would need to find another doctor because he would not treat my baby.”(196)
On November 20, 1993, a nationally syndicated prime-time TV news magazine, The Crusaders, aired a gutsy show on the dangers of the DPT vaccine. Parents of vaccine-damaged children were interviewed, and rare, emotionally wrenching footage of their severely disabled children was shown. While most of the American medical community denies a link between the shots and brain damage or death, listeners heard vaccine expert Dr. Michael Pakickero warn parents that some batches of the DPT vaccine are more toxic than others. And, Dr. John Menkis, the former head of pediatrics and neurology at UCLA, candidly acknowledged, “You will have permanent, irreversible brain damage, which was not present before [DPT] vaccination.” Meanwhile, Michael Settonni, the show’s premier research journalist, estimated from government sources that “at least two children are reportedly killed or injured by the vaccine every day.”(197)
A few days after this show aired, Mr. John Butte, executive producer of The Crusaders, received a scathing letter from Thomas Balbier, Jr., Director of the National Vaccine Injury Compensation Program (VICP), demanding a retraction. He asserted that the number of current vaccine injury and death claims filed by parents during the past few years represent claims of damage “for virtually the entire 20th century.” He also blasted the show for directing listeners to the National Vaccine Information Center (NVIC) — a nonprofit organization dedicated to improving vaccine safety and supporting a parent’s right to choose for or against vaccines. He claimed that NVIC is “not sanctioned” by the federal government, and therefore is “not the official spokesperson” for information on vaccine safety. He also made what appeared to be a veiled threat by noting that copies of his letter were being sent to the U.S. Department of Justice and the Federal Communications Commission.(198)
Note: On January 8, 1994, The Crusaders aired a retraction by quoting the medical industry’s most cherished — and fraudulent — data on the DPT vaccine: a controversial study conducted in Great Britain during the 1950s. Even though 42 of the babies in the study had convulsions within 28 days of receiving the shots, 80 percent of the babies were 14 months of age or older, and the tests were designed to test the efficacy (not safety) of the vaccine, U.S. health authorities still use these results as evidence that the vaccine is safe to give to babies as young as six weeks of age.199 Obviously, the intimidation and coercion ploy was, once again, a wicked success.
On March 19, 1992, Rolling Stone magazine published a remarkable story documenting potential correlations between the first polio vaccines and AIDS. Many independent researchers considered the expos� forthright and extraordinarily well investigated. Several months later, however, the magazine printed a half-page “clarification” indicating that any connection between early polio vaccines and AIDS is “one of several disputed and unproven theories.”200 Evidently, future vaccination campaigns and scientific reputations were jeopardized by the original story.
More examples of the intimidation and coercion ploy:
An Ohio woman with two children killed by the DPT vaccine received threatening letters from the Ohio Department of Health informing her that her only surviving child had to be vaccinated.201 A grieving mother whose baby died 17 hours after receiving a DPT shot was threatened with losing her WIC benefits for refusing to vaccinate her other children.(202)
A Kansas mother who objected to the vaccines was told that the state would seize her child, force the vaccinations upon her, and place her in a foster home. The child was vaccinated and is now permanently disabled as a result of the shot.(203)
This final example of the intimidation and coercion ploy clearly illustrates the arrogant and insensitive nature of the medical community. Grieving and dejected parents who personally contact the Vaccine Adverse Event Reporting System to report how their child was damaged or killed by a vaccine should be forewarned to expect an envelope in the mail with the following bold red letters emblazoned across the front: IMMUNIZE EARLY!(204)
14. The Godfather ploy is an extreme variation of the intimidation and coercion maneuver. It may involve blackmail. For example, poor mothers on state aid in Maryland must now get their children vaccinated or the state will take $25 from their monthly welfare checks for every preschool child not up to date on shots and checkups. A family sanctioned for three months will receive a call from a social service worker, who will request to visit the home to “help resolve the situation and any other problems.” Whereas child advocate groups claim Maryland’s new law is punitive and unfair, the state’s human resources secretary argues that “many [of these welfare recipients] just needed a push to do what is expected of them as responsible parents.”(205)
Here is another example of the godfather ploy: Health insurance companies are threatening to cancel policies when parents refuse vaccines for their children — unless parents sign a form absolving the insurance company from liability if the child contracts certain diseases.(206)
An extreme version of the godfather ploy — framing the parents — is now being reported with increasing regularity by frantic family members. Apparently, medical personnel intent on maintaining the vaccine deception will do anything to deflect blame. Moms and dads who are still grieving over their dead babies following the shots, are now being charged with homicide. For example, one mother, whose healthy baby died just 2 days after receiving DPT and MMR vaccines, was so outraged at this government sanctioned criminal activity, that she tried to fight back with a lawsuit. Authorities responded by charging her with the murder of her child.(207)
15. Scare Tactics. Whenever medical policymakers and their media pawns embark on a promotional blitz to increase vaccination rates, they invariably rely on the scare tactics ploy. Although this stratagem is similar to the intimidation and coercion ploy, subtle differences exist. Practitioners of the intimidation ploy seek mainly to dominate parental decision-making through the sheer force of their will. The scare tactics ruse attempts primarily to manipulate emotions and influence behavior by overstating sad and frightening stories about the unvaccinated.
One recently published pro-vaccine article describes in frightening detail the dangers of nonvaccination. First, readers are informed that “even adults can be killed from preventable infectious diseases.” Next, an emergency room nurse graphically recounts her attempts to restart the heart of a man who had contracted measles and continued to get sicker: A bacteria that usually causes strep throat “had invaded the small holes in the man’s skin” left by his measles rash. The man’s heart couldn’t be restarted, and he died from the secondary infection. Then, to clinch our emotions, we are told that he left three small children.(208)
Note: This very same measles vaccine that authorities claim could have prevented this tragedy, very likely caused it. Prior to the introduction of the measles vaccine, measles was a relatively tame childhood illness, and was virtually unheard of in infant, adolescent, and adult populations. But the vaccine changed all that. Now measles is contracted by age groups more likely to experience extreme complications, including death.(209,210)
A chickenpox vaccine has been available for years; however, authorities have been reluctant to approve it, for many people agree the disease is relatively harmless. Nevertheless, medical forces were prepared to approve it because “the U.S. could save five times as much as it would spend on the vaccine” by avoiding the costs incurred by moms and dads who stay home to care for their sick children. In response to the medical industry’s grand plans to promote this vaccine, media pawns rushed to print fearful stories detailing the dangers of this “serious” disease. For example, one newspaper published a personal story that started with “How my son died from chickenpox.” This scare tactic ruse was coupled with the “I (almost) forgot to mention” ploy, because the child had a preexisting condition that left him vulnerable to infection.(211)
Note: On March 17, 1995, the Food and Drug Administration (FDA) announced that it had approved a chickenpox vaccine.(212) Shortly thereafter, the American Academy of Pediatrics began recommending it for all infants.(213)
16. Euphemisms. Medical personnel often attempt to conceal the facts by using vague terms with hidden meanings — the euphemism ploy. For example, doctors have been notified by the CDC that cases of Hib may occur after vaccination, “prior to the onset of the protective effects of the vaccine.” [Translation: Our vaccine may give your child the disease.] Other studies warn of “increased susceptibility” to the disease in the first 7 days after vaccination. [Another veiled confession that the vaccine may give a child the disease.] In addition, children who contract a particular disease, even though they have received their shots according to the recommended schedule — an earlier schedule that has since been changed (see the variable recommendations ploy) — aren’t the victims of an ineffective vaccine, or a vaccine failure; instead, they were “inappropriately vaccinated.” These are labeled “nonpreventable” cases.(214-216)
In 1993, in England, two of the three MMR (measles, mumps, and rubella) vaccines in use at the time were quietly withdrawn because of what health authorities claim was a “slight” risk of “transient” meningitis.217 A recent study in the United States has determined that the risk of illness and death from childhood shots is real but “extraordinarily low,” leading authorities to conclude that these are “very rare events.”(218) Such remote and fleeting possibilities stand in stark contrast to the words employed by authorities interested in promoting their cause. Then we must be wary of the “poorly developed” immune systems of young children (as an argument in favor of the vaccines!), the “extremely infectious” nature of the virus, and the “grave risk of complications” associated with contracting the disease.(219,220)
More examples of the euphemism ploy:
Researchers are trying to develop a “magic bullet” super-vaccine “that could be given once at birth to immunize infants to all childhood diseases”(221)– delusions of grandeur. Perhaps they call it a “magic bullet” because infant deaths from the “shot” will remain a mystery to the medical scoundrels who pull the trigger.
The public is informed that vaccination rates increase by the time children enter school because parents are “motivated” — not compelled — to have their children vaccinated.(222)
Finally, be wary whenever authorities announce that an “unprecedented” or “experimental” vaccine will soon be available. What they really mean is, “we’re seeking human guinea pigs to study the effects of our newest concoction.”
17. Outright Lies. Lying is an established ploy of the medical community. It is a quick and easy way to promote the vaccine cause without having to rely upon honesty, morality, or ethics. Shrewd members of the medical fraternity know that very few people question doctors and their comrades.
The American Nurses Association recently collaborated with Every Child by Two, the Rosalynn Carter/Betty Bumpers Campaign for Early Immunization, “to educate nurses, parents, business leaders, civic organizations, and educators about the urgent need to immunize children.” Their aggressive stance against unvaccinated children includes a news release with the following claim: several childhood diseases — including polio, diphtheria, rubella, mumps, and tetanus — are undergoing a “resurgence.” This statement is an outright lie, obviously made to scare parents into vaccinating their children. None of these diseases is making a comeback. In fact, all are at their lowest rates of occurrence since records on their existence have been kept.(223)
According to Donna Shalala, President Clinton’s secretary of Health and Human Services, “This year’s flu, the Beijing strain, is expected to hit very hard.” She also claimed that 10,000 to 45,000 Americans lose their lives to influenza each year.224 However, official government statistics, which Donna Shalala oversees, contradict her claim. In 1991, the CDC reported just 990 deaths attributable to influenza; in 1992, 1,260. Americans die at rates 3 or 4 times greater from common diseases such as asthma (4,650 deaths in 1992), stomach ulcers (5,770 deaths in 1992) and nutritional deficiencies (3,100 deaths in 1992).(225)
18. Variable and Illogical Recommendations. Our children are being used as guinea pigs. To conceal this fact, authorities frequently change their recommendations. New and experimental vaccines replace old and ineffective ones. The number of doses and ages to receive them are altered on a regular basis as well, often with little rationale to justify either the original recommendation or the switch. For example, in 1985 the first Hib vaccine (haemophilus influenzae type b) was approved for general use in the United States and was quickly recommended for all children two years old and up —even though 75 percent of all Hib cases occur before two years of age! In 1988, a new “conjugated” Hib vaccine was approved for use in children at least 18 months of age. By 1991, its recommended use was extended to infants as young as two months old. Today, a genetically engineered Hib vaccine has replaced all earlier versions.(226-229)
In 1963, the recommended age for measles vaccination was 9 months. In 1965 it was changed to 12 months. In 1976 it was changed to 15 months.(230) However, since fewer moms have natural immunity to measles today — due to the large number of mothers who received childhood shots in the 1960s, 1970s, and 1980s — and therefore cannot pass protective antibodies on to their infants, outbreaks of cases are now occurring in children under 15 months of age.(231) In fact, by 1993, more than 25 percent of all measles cases were appearing in babies under one year of age.(232) As a result, in some areas of the country the recommended age to receive the measles vaccine was lowered again, bringing us full circle to initial recommendations — when most children were, according to medical authorities, “inappropriately vaccinated!”(233)
Recent data indicates that a large majority of measles cases are occurring in vaccinated people.(234) To conceal this fact, authorities rely upon the variable recommendations ploy and now recommend a measles booster shot at 4 to 6 years.(235) Some schools are requiring proof of revaccination before children can enter the 7th grade. Many colleges are refusing to admit students who have no evidence of revaccination. Yet, earlier studies — one recently published in the Pediatric Infectious Disease Journal — demonstrated that booster doses of the measles shot are relatively ineffective.(236,237)
Are altered recommendations based on sound science or personal convenience? Vaccine policymakers anxious to introduce the chickenpox vaccine were stymied by the number of vaccines already in existence. They could not decide at what age to recommend their new product. They wanted to make room for it at 15 months, but that would necessitate changing the third of four recommended ages to receive the oral polio vaccine from “15 to 18 months” to “6 months.” However, because there is “more leeway” with the MMR vaccine, they considered changing the first of three recommended ages to receive it from “15 months” to “12 to 15 months.”(238)
A “plasma-derived” hepatitis vaccination was introduced in the 1970s. In 1987, a genetically engineered “yeast-derived” vaccine was developed. In 1991, the CDC and AAP began the process of mandating the new vaccine for all infants — even though adult IV drug users, not children, are most at risk of contracting this disease!(239)
Here is one final example of the variable and illogical recommendations ploy: Authorities are so incensed by the number of people claiming vaccines damaged or killed a family member, that they are seeking to further restrict the stringent criteria for entering the National Vaccine Injury Compensation Program. For example, the newly revised rules stipulate that a severe reaction to a DPT vaccine — such as anaphylactic shock — must occur within 4 hours! In other words, if your previously healthy child receives the vaccine at 10 o’clock in the morning, has a violent allergic reaction — gasps for air, collapses into unconsciousness — at 3 o’clock that afternoon, and is later diagnosed as brain damaged, the federal government will say that the damage is not related to the shot and therefore you don’t have a claim. Other criteria for entering the program have been restricted as well, or removed altogether.(240)
19. Adjustable Diagnoses and Exaggerated Epidemics. Health officials realized early on that vaccine efficacy rates could be maximized by creative diagnoses. Remember, “the credit of vaccination is kept up statistically by diagnosing all the [cases of smallpox after vaccinations] as pustular eczema [or anything else] except smallpox.”(241) In other words, if the nonvaccinated contract the disease, call it one thing; if the vaccinated become ill, name it something else.
The medical profession often goes to great lengths to create the illusion of extraordinary vaccine efficacy rates. As an example, the standards for defining polio were changed when the live-virus polio vaccine was introduced. The new definition of a “polio epidemic” required more cases to be reported (35 per 100,000 instead of the customary 20 per 100,000). At this time paralytic polio was redefined as well, making it more difficult to confirm, and therefore tally, cases. Prior to the introduction of the vaccine the patient only had to exhibit paralytic symptoms for 24 hours. Laboratory confirmation and tests to determine residual (prolonged) paralysis were not required. The new definition required the patient to exhibit paralytic symptoms for at least 60 days, and residual paralysis had to be confirmed twice during the course of the disease. Finally, after the vaccine was introduced cases of aseptic meningitis (an infectious disease often difficult to distinguish from polio) were more often reported as a separate disease from polio. But such cases were counted as polio before the vaccine was introduced.(242,243) The vaccine’s reported efficacy was therefore skewed.
More recently, two siblings contracted a bad cough, and they were brought to the family doctor for a checkup. In a separate visit, their 2 cousins, who also contracted a bad cough, were brought to the same doctor. Prior to being examined, the doctor asked each set of parents the vaccine status of their children. The first 2 children, who were not vaccinated, were diagnosed as having pertussis. The other 2 children, who had been vaccinated against pertussis, were diagnosed as having bronchitis. No clinical test was performed on any of the children.(244) This tactic serves two functions: 1) it inflates whooping cough statistics suggesting the need for a pertussis vaccine, and 2) it suppresses the truth that the vaccine is ineffective.
Babies who die soon after receiving vaccinations are often diagnosed with Sudden Infant Death Syndrome (SIDS). In fact, this tactic is so handy that coroners are permitted to use this term to certify toddler deaths up to the age of 24 months.(245,246)
Vaccine epidemics are often “created” when health officials misdiagnose ailments, or overstate the number of cases. As an example, when television programs challenged the safety of the pertussis vaccine, the Maryland Health Department deceived the public by blaming a new “epidemic” of whooping cough on the impact of these shows. When Dr. J. Anthony Morris, former top virologist for the U.S. Division of Biological Standards, analyzed the original data, however, he concluded the Maryland epidemic didn’t exist. In only 5 of the 41 cases was there reasonable evidence to correctly diagnose whooping cough. And each of these 5 children had received from one to four doses of the pertussis vaccine.(247)
In Placitas, New Mexico, headlines warned parents of a dangerous whooping cough “epidemic” in that town. But only three cases of whooping cough were discovered, two of them in siblings, all three of them in children who were vaccinated.(248)
20. Patriotic Duty and Social Responsibility (also known as the Guilt Trip). According to Dr. Martin Smith of the American Academy of Pediatrics (AAP), “children of the nation are soldiers in the defense of this country against disease.”(249) Vaccine advocates maintain that some children must be sacrificed “for the welfare, safety, and comfort” of the nation.(250) One mother, whose child was permanently brain damaged within hours after receiving a DPT vaccine, was told by the family doctor that this was the price her child had to pay to keep other children safe. According to Dr. George Flores, Sonoma County public health officer, parents who reject vaccines “don’t consider the effect of their child on the rest of society.”(251) Apparently, unvaccinated children are a danger to everyone who is vaccinated, even though the vaccinated are supposed to be “protected.” (We are told that for the shots to work, everyone must play along.)(252) And families who decline the shots, we are told, are somehow reaping the benefits from those who dutifully have their children vaccinated.(253)
21. Unethical Experimentation. In December 1990, a federal regulation was adopted whereby the FDA gave permission to the U.S. Department of Defense (DoD) to circumvent U.S. and international laws forbidding medical experiments on unwilling subjects. This is the decree that allowed the DoD to inject American Gulf War troops with unapproved experimental drugs and vaccines without their informed consent by deeming it “not feasible” to obtain the soldiers’ permission.(254) Today, many of these vets, their spouses, and their children, are crippled by unknown diseases.(255)
In a class action lawsuit, American Indians in South Dakota are suing the FDA and CDC for testing a new hepatitis A vaccine on their infants. Health officials did not warn the parents the exposed children would be at risk for cancer, convulsions, eye disorders, or death.(256) Authorities now plan to test hepatitis A vaccine on remote Northwest Alaska villagers.(257)
Simultaneously administered vaccines have not been proven safe, yet authorities continue to recommend them and medical health practitioners continue to inject them. A recent study in the Journal of the American Medical Association found lowered levels of pertussis antibodies in children who were simultaneously given the DPT and Hib vaccines. According to the author of the study, “This concern must be addressed, for obviously we do not want to expose our children to the risk of vaccines without providing them with optimum benefit.”(258)
Every year during the fall and winter seasons a new flu virus is thought to circulate throughout the community. To produce a vaccine for this virus, health officials must correctly predict nearly a year in advance which virus will arrive (causing some people to speculate that when officials guess correctly, it’s really the vaccine itself that may be spreading the disease). With production usually beginning in January, and the final product licensed by the FDA in August, just a month or two before the shots are distributed, who does it seem the vaccines are being tested on?(259)
Vaccine researchers perform unethical experiments on human populations whenever their newest creations are ready to be tested. Therefore it comes as no surprise to learn of their plans to add foreign substances — viral matter — to the food supply. In fact, biotechnology firms have been experimenting with adding vaccines to bananas, lettuce, potatoes, tomatoes, and soybeans for several years now.(260,261) Who do you think these vaccines will be tested on?
22. Mandates. If vaccines are so wonderful, why does the government need to mandate them? You’d think that everyone would be lining up to get the shots. But vaccination rates are modest. The Clinton administration claimed that the price and accessibility of vaccines were hindering parents from maintaining vaccine schedules.(262) However, according to a survey conducted by The Gallup Organization on behalf of Lederle Laboratories, a major vaccine manufacturer, the “cost and time involved are least important” considerations for parents deciding whether to vaccinate their children. “The possibility of side effects is most frequently rated as important in making the decision.”(263)
State laws require children to be vaccinated before they can enter public school — unless a parent signs a waiver indicating opposition to the shots. While some states offer a philosophical or religious exemption, all provide a medical exemption — if contraindications exist. But parents should not have to sign a waiver objecting to mandatory vaccines. Instead, those who elect to have their children vaccinated should be obligated to read the full range of possible adverse reactions. Then, parents who still elect to have their children vaccinated should be required to sign a form indicating that they understand all the risks involved.
Mandating vaccines is also an unscrupulous means of extorting money from trusting parents. Imagine the exorbitant profits of any company that produces a product everyone is required by law to buy — even against their will. Moreover, the extreme wealth acquired through this medical racket is not hoarded by the drug makers alone; common doctors share in the booty. According to the late Dr. Robert Mendelsohn, world-renowned pediatrician, vaccines are the “bread and butter” of pediatric practice.(264) Others speculate that the damage caused by the shots may be responsible for new ailments and rare diseases(265-267) — enough to keep medical specialists affluent and busy for years to come.
Imagine for a moment a group of nutritionists who develop a multivitamin. They place their own people in a position to evaluate the benefits and risks of the product. It is now “officially” declared safe and effective. In fact, children who take this new multivitamin are reported to be 50 percent healthier than other children. But there is a catch: the costly vitamins must be taken at regular intervals and everyone must take them or they won’t work. They won’t enhance health, we are told, because the disease-prone “unprotected” children — progeny of irresponsible parents — will pass their germs on to the “protected” children — children of “responsible” families. So the nutritionists lobby government officials to mandate their product. Busy lawmakers study the “official” study results, determine that “protecting” children is a high priority, and decide to support the goals and ambitions of this powerful lobbying force.
Imagine any coalition of professionals with an agenda to pursue. Say, a guild of hypnotists has determined that children can be hypnotized to perform better in school than children who are not hypnotized. But again there is a catch: the children must be taken from their parents at regular intervals to be hypnotized, and all children must be hypnotized or the effects will be incomplete. Would you agree to this practice? Mind control, body control; who has authority over our children?
23. Refusing to Report Vaccine Reactions. Despite a federal law passed by Congress in 1986 — the National Childhood Vaccine Injury Act — requiring all doctors who administer vaccines to report vaccine reactions to federal health officials, many choose to ignore this legal requirement. Doctors often justify their refusal to report vaccine reactions by claiming the shot had nothing to do with the child’s injury or death. The will of Congress is being subverted, resulting in a gross underreporting of vaccine injuries and deaths.(268)
The Vaccine Adverse Events Reporting System (VAERS) is the federal program designated to tally reports of vaccine injuries and deaths. By the year 2002, tens of thousands of reactions to vaccines, including deaths, were reported — despite the medical boycott against reporting incidents.(269) Still, one must magnify these figures tenfold, because the FDA estimates that 90 percent of doctors do not report incidents.(270)
To further confirm the degree of underreporting that occurs, in 1988 and 1989 Connaught Laboratories conducted a study to determine the true rate of adverse events associated with the vaccines they produce. During this period of time, unsolicited (“spontaneous”) reports of adverse events occurred at the rate of 20 per million doses. However, when they supplied the vaccine to doctors with a request to report any adverse event that occurred within 30 days of a vaccination, provided that it resulted in a physician visit, the rate of adverse events skyrocketed to 927 events per million doses. According to Dr. Jim Froeschle, director of clinical research at Connaught Laboratories, these differences indicate “a fifty-fold underreporting of adverse events.”(271) Yet, even this figure may be conservative. According to Dr. David Kessler, M.D., director of the Food and Drug Administration, “Only about one percent of serious events [adverse drug reactions] are reported to the FDA.”(272)
The following testimonials from parents and relatives of vaccine-damaged children illustrate how easily doctors can dismiss apparent vaccine reactions and thus justify not reporting them:
“Our son had his 2nd DPT shot and oral polio [vaccine] at four months of age on September 22, 1989. He had reacted to his 1st DPT immunization two months earlier with prolonged high-pitched screaming and projectile vomiting…. After his 2nd shot he immediately started the high-pitched screaming again. He could no longer hold his head up and could not keep his food down. He couldn’t sleep or stay awake, he had absence seizures, dozens to hundreds a day. He deteriorated daily and died April 14, 1990.” The doctor would not report this reaction. He did not feel that it was related to the vaccine.
“Our 16-month-old grandson received his 4th DPT shot on December 5, 1989, and he died 24 days later. He also received the MMR and oral polio vaccines at the same time. Within 24 hours his legs were red and swollen, he had a fever of 103 degrees, and he was very fussy and irritable…. His previous shots had similar reactions…. We know the shot contributed to his death.” The doctor would not report this reaction. He did not feel that it was related to the vaccine.
“We lost our beautiful, precious and adored 4-month-old son 26 hours after receiving the DPT vaccination and oral polio [vaccine] at his well-baby checkup on January 25, 1990…. We were aware our son’s behavior patterns changed after the shot…. He was staring, looked spacey, only took short naps, vomited his bottle…. The doctor was insistent that this was a SIDS death.” The doctor would not report this reaction. He did not feel that it was related to the vaccine.
“Our son had his 1st DPT vaccination and oral polio vaccine at 14 months old on February 22, 1990. That evening he started high-pitched screaming. The next two days he had a temperature of 101 degrees and slept for 15 hours. When he awoke he was extremely irritable…. My son was in a lot of body pain. At times he looked like he had a stroke. At other times he was curled up in a hard knot we couldn’t straighten. He was having seizures and we didn’t know it…. He continues to have seizures. The doctor, even though law required him to record manufacturer and lot number, did not record the number.” The doctor would not report this reaction. He did not feel that it was related to the vaccine.
“My son had his first DPT shot at his 2-month checkup on May 8, 1990…. Four hours later he started crying…. I noticed he was pale and like a statue…. He stopped breathing. I picked him up and shook him and he started breathing again. A friend was visiting and called 911. My son stopped breathing 8 to 10 more times with me shaking him out of it each time before the paramedics arrived. He was ash white…screaming when we got to the hospital…. I have another child who had severe reactions from his shots. He had a seizure after each of his first three DPT shots and was on medication for three years.” The doctor would not report this reaction. He did not feel that it was related to the vaccine.
“My 16-month-old grandson had his 2nd DPT shot, MMR, and polio at his well-baby checkup on August 16, 1990. In less than 48 hours he had a temperature of 105 degrees and went into convulsions…. My grandson has deteriorated daily. He walks stiff-legged, or his knee collapses on under him…. He has trouble with his bowels, constipation one minute followed by diarrhea running down his leg the next minute. We look at our old videos and realize how much he has changed.” The doctor would not report this reaction, nor would he give the parents the manufacturers, and lot numbers of the vaccines he administered.
“My grandson had his 1st DPT shot and oral polio [vaccine] at his 2-month well-baby checkup on June 8, 1990. Within 21 hours he was dead. After the shot he started crying [high-pitched screaming]…. My grandson began projectile vomiting and continued the high-pitched crying…. At 7 A.M. my daughter awoke and found my grandson to have a purple color on one side of his face, clenched fists, blood coming from his nose and mouth and not breathing. My grandson was dead. I have promised my daughter that his death will not be in vain and just another statistic labeled SIDS.” The doctor would not report this reaction. He did not feel that it was related to the vaccine.(273)
24. Suppress Information/Prohibit Conflicting Testimony. On April 1, 1993, several bills were introduced in Congress to establish a federal “tracking and surveillance” system that would monitor parents who choose not to vaccinate their children. A few weeks later, Representative Henry Waxman and Senator Ted Kennedy chaired “public” hearings on this legislation, but prohibited input from individual parents, parent organizations, and healthcare professionals concerned about vaccine safety. Instead, only groups with a vested interest in ratifying these bills were permitted to attend: White House sponsors, several presidents of multibillion dollar companies that produce vaccines, agents of the American Academy of Pediatrics, and public health officials.(274)
The Salk “inactivated” or “killed-virus” vaccine was actually regulated to permit 5,000 live viruses per million doses. Yet, because the vaccine was promoted as being incapable of causing polio, cases that occurred following administration of the vaccine were denied, and it was excluded from the Vaccine Injury Table.(275) The CDC also refuses to acknowledge occurrences of encephalitis and seizure disorders following administration of the oral polio vaccine, even though encephalitis has been known to occur following polio contracted under natural conditions.(276)
More examples of the suppression ploy:
A recent report published in Lancet notes that some people contract meningitis after receiving the MMR vaccine. Nevertheless, the author concludes that “because of the extreme rarity of this complication, parents need not be told about the risk before deciding on vaccination.”(277)
Even though a national drug evaluation committee (ADRAC) recommended that children should be observed for a sufficient period of time after vaccination to monitor reactions, authorities fought against the suggested period of observation on the grounds that it causes inconvenience to parents and increases anxiety about the safety of childhood shots.(278)
When the National Childhood Vaccine Injury Act of 1986 was passed into law, the Department of Health and Human Services (HHS) was ordered by Congress “to develop and disseminate vaccine information materials for distribution by health care workers.” This material was to include information on adverse reactions, contraindications, and the availability of a federal compensation program for people who are injured or die from a mandated vaccine. HHS was to satisfy this legal requirement by December 22, 1988. By March 4, 1991, this matter was still unsettled. When HHS eventually submitted the required information, “they failed to meet even minimal standards of scientific rigor, candor, and fairness.” Vaccine risks were systematically understated or ignored.(279)
Although medical personnel are required by law to provide their clients with information booklets explaining the benefits and risks of vaccinations before they receive their shots, few doctors offer these booklets to their clients. The following story illustrates the type of damage that can occur when healthcare providers choose to suppress lifesaving information:
“I am a 29-nine-year old female who received an MMR vaccine required by [the medical center where I work]. Since receiving that vaccine I’ve experienced a number of side effects: dizziness, headaches, numbness of my feet and ankles, shortness of breath, chest pain, and aching joints.
“I have seen several doctors over the last six months, more times than I can count. Those doctors that admitted the vaccine may have something to do with these symptoms felt that within six months the symptoms would subside. Unfortunately, this is not the case. In fact, some symptoms have gotten worse. My ankles are numb almost continuously, the chest pain has begun to include pain in my left arm and jaw, accompanied by difficulty breathing.
“Every aspect of my life has been affected by this, including my work ability, which is the reason I had to have the vaccine in the first place. I was told I either had to get it, or I wouldn’t have a job. Unfortunately, by this time I have already given up the job I held for over five years.
“I was not given any information prior to receiving the vaccine. [I later learned] that people allergic to eggs should not receive this vaccine. I am allergic to eggs, but the hospital staff never asked or told me anything. My primary care physician is at a loss about what to do with me. But I continue to suffer.”(280)
25. Psychological Projection. Medical personnel are notorious for seeing in others the very thoughts, feelings, and actions they deny in themselves. This subtle and unconscious defense against anxiety and guilt is what psychologists refer to as projection. Vaccine researchers, for example, are disappointed that women and minorities have been reluctant to be experimented on with a new AIDS vaccine, even in light of recent revelations about Cold War radiation tests on unwitting subjects. The reluctant volunteers — not the researchers — were blamed for harboring a “mistaken belief” that the vaccine could cause AIDS, despite what the scientists say.(281)
Note: Less than 5 months later, researchers were forced to acknowledge that “at least five volunteers in the government’s principal AIDS vaccine study have become infected with the AIDS virus after receiving the vaccine.” One of the subjects is said to have undergone “an unusually rapid decline in the number of white blood cells, the standard measure for the progress of AIDS.” This has raised researchers’ concerns “not only about how well the vaccine works but whether it may have increased the likelihood of their infection and…even accelerated the progression of disease.”(282)
Medical policymakers and some lawmakers claim parents are abusing their children by not allowing them to be vaccinated.(283,284) Some parents have been accused of child abuse — “shaking baby syndrome” — after their children had seizures or went into a coma following vaccinations.(285) In fact, the authorities who allow these dangerous vaccines to be administered are abusing the children and implicating the parents. Parents have lost custody of their loved ones in this manner.(286)
26. Organized Propaganda. Community organizations and parent groups are often enlisted by medical associations to help organize campaigns against unvaccinated children. “Volunteers” rarely question the cult-like doctrines the pro-vaccinators foist in their direction. But are these organizations, and their helpers, really doing the community a service? How honest are vaccine campaigns that omit mention of the thousands of families affected every year by adverse reactions to vaccines? Why are the true facts prohibited from being revealed? And why can’t parents be trusted to weigh the facts for themselves?
The medical-industrial complex is well-prepared for almost any unfavorable eventuality that may occur. For example, soon after the NBC television show “NOW” broadcast a story about the dangerous DPT vaccine, a DPT manufacturer sent telegrams to health professionals throughout the nation reassuring them of the vaccine’s safety.(287) After the show aired a second time, the CDC organized a propaganda blitz by swiftly faxing biased pro-vaccine information to doctors and other concerned people throughout the nation. In this fax, the CDC had the audacity to claim that “Almost all infants with any medical illness, including death, will have been vaccinated earlier in their life…. [and] Almost all infants with any medical illness, including death, will have drunk milk earlier in their life,”(288) implying that receiving shots is as benign as drinking milk.
27. Legal Immunity. When the FDA tested a batch of DPT vaccine, they found the entire lot to be 200 percent more potent than regulations allowed. Instead of immediately destroying it, the agency allowed health authorities to “test” it on hundreds of children in Michigan. This proved to be a tragic gamble. Later, when the parents of children who were paralyzed and brain damaged from the mandatory shots tried to sue the state, the courts disallowed their case because the “doctrine of sovereign immunity” protects the government from claims arising from services that only the government can provide.(289)
A 13-year-old Pennsylvania girl suffered irreversible brain damage from a measles vaccine received during a mandatory mass vaccination program at her school. However, a court decision made it clear that neither the vaccine manufacturers nor the government could be held responsible because the vaccines were “unavoidably unsafe.” [Translation: Parents are compelled to play the medical establishment’s unique brand of Russian roulette.] The court also claimed the vaccine maker adequately delineated risks on its package insert.290 Consequently, these parents were deemed solely responsible for the care of their now mentally retarded daughter — even though they, like most parents, were not warned about vaccine dangers, were not told about these inserts, and withheld permission for their daughter to be vaccinated!(291)
Drug companies are legally immune against most claims of vaccine damage, and their incentive to produce safer vaccines was removed when the National Childhood Vaccine Injury Act of 1986 was passed. This law states that “no vaccine manufacturer shall be liable in a civil action for damages arising from a vaccine-related injury or death.” Incredibly, the original draft also stated: “The term vaccine-related injury or death means an illness, injury, condition or death associated with one or more of the vaccines listed in the vaccine injury table except that the term does not include an illness, injury, condition or death associated with an adulterant or contaminant intentionally added to such a vaccine.”(292)
28. Threats to go out of Business. Before the National Childhood Vaccine Injury Act of 1986 was enacted, vaccine manufacturers were being sued so often and for so much money, that many threatened to — and did — go out of business.(293) When the government began accepting liability for vaccine injuries and deaths, the enterprising drug companies succeeded in removing an important incentive to produce safe and effective vaccines.
29. Stonewalling. Vaccine officials use the stonewalling tactic whenever they want to delay or avoid accepting accountability. For example, when one mother, whose son died four days after his second polio shot, studied his provisional autopsy report, she noted that there were major findings of myocarditis, and hepatitis, and that the polio virus had been extracted from these diseased organs — conditions not inconsistent with a vaccine reaction. But when she questioned the pathology department’s initial conclusion — Sudden Infant Death Syndrome — and requested additional tests to determine whether the polio virus was a wild or vaccine strain, she was led into a nine-year battle with the CDC to secure the results. (Medical authorities were forced to concede the truth: the vaccine caused the child’s polio.)(294)
When a child is killed by a mandated vaccine, the government is expected to compensate the parents, awarding them up to $250,000. However, if the child is seriously injured by the vaccine, continues to live, and requires lifetime care, several million dollars may be awarded. Government officials may be reluctant to settle cases quickly, hoping the damaged child will die, thereby lowering the payment. This is exactly what millions of people learned when The Crusaders, a television newsmagazine, aired a gutsy show on the dangerous pertussis vaccine. The father of a young boy who suffered severe and permanent brain damage just hours after a DPT shot could not get the government to settle his case. The family needs the money to pay for the child’s specialized care, but “if something were to happen to him and he did not live, they would not have to pay for his life care.”(295)
30. Secrecy. If vaccines offered benefits only, the government wouldn’t need to mandate them, and the ploys noted in this chapter wouldn’t be necessary. Instead, parents would be lining up to get the shots. Members of the medical fraternity realize this, and have banded together to conceal how the vaccines are made, who they’re tested on, how effective they really are, and the true rates of adverse events. Even the manufacturer’s cost to market vaccines is considered a “trade secret or confidential information.”(296)
Doctors who have dared to publicly question vaccines, “have been warned that their careers are at stake and they risk [losing their license to practice medicine].”(297) Others are discredited.(298)
After one family’s son was damaged by a DPT shot, they obtained, through the Freedom of Information Act, a computerized record of more than 34,000 adverse reactions to vaccines over a three-year period. They had a hunch their son had received a bad vaccine — from a “hot lot” — and wanted to see if they could protect other children from being hurt.
After a great deal of research, they discovered that their son had been vaccinated from a hot lot. The death rate associated with this batch was three times higher than that linked with other lots. Ten children had died from it. But when the parents spoke to officials at the FDA to determine if the agency would conduct an investigation, they were told that “due to the size of the lot, the deaths did not warrant significant investigation.” When they inquired about the size of the lot, the FDA flatly stated, “That’s confidential.”(299)
Parents everywhere would like to know how many deaths would be enough to warrant an investigation. If ten isn’t enough, is twenty? Thirty? Forty? What’s enough? What industry is permitted to operate in secrecy, and put out a product to the public without accountability? Concerned citizens cannot even find out from the government what the mechanism is to institute a recall, if indeed one even exists.(300)
Drug company awards for vaccine damage are usually settled out of court. Parents who expect to receive compensation for their child who was damaged or killed by a vaccine are often obligated to remain silent as a condition of the agreement. Parents seeking compensation from the Federal Vaccine Injury Compensation Program are often counseled to refrain from discussing their cases, and settlements, as well.(301) To learn how difficult it is to break the secrecy pact, try to obtain specific vaccine information from the CDC or FDA. They’ll be happy to send you their official propaganda but will quickly turn apprehensive and restrained when you start probing for additional information. These public organizations, supported by taxpayer dollars, have all sorts of information. However, they’re unlikely to share it with average citizens, for then we’d be able to make our own rational, informed decisions regarding the shots. But the American people are entitled to know the answers to their questions before submitting their children to “mandated” vaccines.
“We could kneel on broken glass and give the American Medical Association (AMA) everything it wanted, and still they will oppose it. They are going to push us as far as possible, and then they are just going to screw us.” –Federal Healthcare Task Force Member, Time, (September 20, 1993), p. 61. “Every doctor will allow a colleague to decimate a whole countryside sooner than violate the bond of professional etiquette by giving him away.” –George Bernard Shaw
This article was excerpted from the vaccine archives of Neil Z. Miller.
See Immunization Theory vs. Reality for more information.
Copyright © 1995-2003. All Rights Reserved.
The Truth About the Drug Companies:
How They Deceive Us and What to Do About It
In this book, her most recent, Marcia Angell explores pharmaceutical research, deplores the rapidly expanding involvement (and distortion of truth) of Big Pharma, and implores us all (physicians, patients, politicians) to do something about it. The dust-jacket blurb asserts that Angell, “during her two decades at The New England Journal of Medicine had a front-row seat on the growing corruption of the pharmaceutical industry.”
Since leaving the Journal, she’s gone behind the curtains of Big Pharma, Big University, and Big Faculty. Drawing on her own work and on her thoughtful analysis of research, company financial statements, and investigative reports into drug development and marketing, Angell writes with the unambiguous and unyielding style that Journal readers came to expect and trust.
The current slide toward the commercialization and corruption of clinical research coincided with the election of President Ronald Reagan in 1980 and the passage of the Bayh-Dole Act, a new set of laws that permitted and encouraged universities and small businesses to patent discoveries from research sponsored by the National Institutes of Health (NIH). Research paid for by the public to serve the public instantly became a private, and salable good—one that is producing drug sales of more than $200 billion a year.
Commercialization had both specific and broad effects. Readers of this journal and others are familiar with investigations into the control that research sponsors at pharmaceutical companies exert on the design and analysis of clinical trials (including the distortion of primary outcome measures in trials) and the issue of reporting, nonreporting, and biased reporting of results.
Angell reminds us of the increasingly cozy relationships between big industry and the faculties of universities. Not only are narcissistic donors renaming the medical schools; they are buying access to the best minds of their faculties. Angell’s examples of the large consulting fees paid by industry to individual faculty members and to NIH scientists and directors are astounding.
The broader effects are felt in the commercialization of universities, medical faculties, and our profession. In 2000, in a letter written in response to Angell’s Journal editorial, “Is Academic Medicine for Sale?” a reader supplied the answer: “No. The current owner is very happy with it.” The increasing intrusion of industry into medical education and the almost complete domination of continuing medical education (especially regarding drugs) by the marketing departments of large pharmaceutical companies are a scandal.
The same companies also spend heavily to lobby governments. According to Angell, Pharmaceutical Research and Manufacturers of America, the pharmaceutical industry’s U.S. trade association has “the largest lobby in Washington,” which in 2002 employed 675 lobbyists (including 26 former members of Congress) at a cost of more than $91 million. The result has been above-average growth in corporate profits during both Republican and Democratic administrations.
The most recent and perplexing lobbying effort caused Congress explicitly to prohibit Medicare from using its huge purchasing power to get lower prices for drugs, thus opening up a dollar pipeline, in the form of higher drug prices, directly from taxpayers to corporate coffers. These changes, along with the cave-in by the Food and Drug Administration (FDA) in 1997 that permitted direct-to-consumer advertising to bypass mention in their ads of all but the most serious side effects, have further augmented profits. The overall effect has been a corruption not only of science but also of the dissemination of science.
Angell documents that, contrary to what they claim, large pharmaceutical companies have “paltry output” in innovative research. In fact, as permitted by Bayh-Dole, pharmaceutical companies buy discoveries coming out of the basic-science enterprises, including universities and publicly funded granting agencies. The real costs of research on drugs by pharmaceutical companies are much less than the oft-quoted $800 million or so per new drug brought to market. Most of their research is on me-too drugs—unoriginal, tax-deductible (and thus paid for in lost taxes by the public), and mostly unnecessary. The Big Pharma companies are, in essence, manufacturing and marketing companies.
Angell’s concluding chapter, the least convincing in an otherwise fascinating and penetrating book, contains the solutions, all of them predictable: control me-too drugs, re-empower the FDA, oversee Big Pharma’s clinical research, curb patent length and abuse, keep Big Pharma out of medical education, make company financial statements transparent (so we can tell what the costs of research really are, as distinct from marketing), and impose price controls or guidelines. Granted, the problems are so prevalent and the corporate tentacles so entwined with our way of being that it is hard to see what else to recommend.
But perhaps Angell is right. We must change the way we manage research and the development and distribution of new drugs. Not only are health and health care at risk, but so are the research enterprise and the reputations of universities and governments. The integrity of scientific research is too important to be left to the invisible hand of the marketplace.
John Hoey, M.D.
New England Journal of Medicine
Volume 351:1580-1581, October 7, 2004, Number 15
http://content.nejm.org/cgi/content/full/351/15/1580 (payment required to view article)
For a riveting 10-page summary of Dr. Angell’s book, click here
NewsTarget) Archived documents discovered at the U.S. Food and Drug Administration’s website reveal the agency knew in 2003 that HPV infections did not cause cervical cancer. Despite that knowledge, the FDA has continued to support the use of the Gardasil vaccine in compulsory vaccinations programs like the one announced in Texas earlier this year.
The FDA’s own press release from 2003 admits that, “Most women who become infected with HPV are able to eradicate the virus [without intervention] and suffer no apparent long-term consequences to their health… most infections are short-lived and not associated with cervical cancer.” (Source: “FDA Approves Expanded Use of HPV Test,” March 31, 2003, http://www.FDA.gov)
Mike Adams, the Health Ranger, an independent consumer health advocate who opposes compulsory vaccinations, has unleashed a volley of multimedia files designed to expose the scientific fraud behind Gardasil vaccines while educating the public about the real health risks that may be associated with HPV vaccinations. His special report, “The Great HPV Vaccination Hoax Exposed” is available now at:
Adams has also created a 10-minute YouTube video highlighting the scientific fraud behind HPV vaccinations: http://www.youtube.com/watch?v=XK97CHQZhq0
Adams has also posted a 45-minute audio report on the HPV vaccination fraud. It’s called the Health Ranger Report and features a detailed discussion of the evidence showing the scientific fraud and fear mongering that’s powering Big Pharma’s mandatory vaccination push in America today. The program is available for immediate download as an MP3 file at: http://www.NewsTarget.com/podcasts/HRR015_HPV_48.MP3
In addition, Adams participated earlier today in a fast-rising podcast show called Real Health with Dr. Steve which features multiple guests in a fast-paced, information-rich format. The show is now listed on iTunes and can be accessed directly at: http://web.mac.com/drsteve720/Site/Podcast/Podcast.html
(The Adams interview on HPV Vaccinations is found in show #11, which was not yet posted at the time of this story, but should appear within 2-3 days.)
Finally, Adams joined nutritionist Jonny Bowden and Sugar Shock author Connie Bennett in an unrelated (but very entertaining and educational) audio show today. The Sugar Shock BlockTalkRadio show is available for live listening now at: http://www.blogtalkradio.com/stopsugarshock
These are all part of Mike Adams’ efforts to educate the public on the truth about mandatory vaccination programs, which he says are deceptively marketed and based on “scientific fraud.”
FDA and HPV — when did they know the truth?
Cynthia A. Janak
Cynthia A. Janak
December 12, 2007
First, I want to say thank you to everyone reading my articles. Your emails show me your curiosity and concern about what is happening in the world today warms my heart.
In my last article about Gardasil I quoted a document that I found on the FDA website called the “Reclassification Petition for Human Papillomavirus (HPV) DNA, Nested Polymerase Chain Reaction (PCR) Detection” published March 7, 2007.
What I have done is read all 68 pages of this document. What I am going to show you is that the FDA knew back in 2003 that a HPV is not the actual cause of cervical cancer. The actual cause is a “persistent HPV infection that may act as a tumor promoter in cancer induction [8-11].
I want you to take note of “persistent HPV infection” and “self-limiting.” These terms are stated throughout the document and very important to what I am going to show you. Here are the definitions. At the end of the document I will have further definitions of some of the terms that are used in this document.
Persistent-Function: adjective Etymology: Latin persistent-, persistens, present participle of persistere Date: 1826, 1: existing for a long or longer than usual time or continuously: as a: retained beyond the usual period persistent leaf>
Self-limiting-Function: adjective Date: 1863, : limiting oneself or itself; especially of a disease : SELF-LIMITED Function: adjective Date: 1845, : limited by one’s or its own nature; specifically : running a definite and limited course self — limited disease>
What I am going to do is quote segments of this document and highlight what I consider is important to the average person. I know this is going to be long but to summarize would be an injustice to the authors of this document.
VI. Statement of the basis for disagreement with the present classification status
[21 CFR § 860.123(a)(5) ]
The basis of this reclassification request is that the present regulatory classification of HPV DNA tests as devices intended for use in identifying and typing HPV infection to stratify women at risk for cervical cancer, thus assigned to class III, requiring submission and approval of PMAs , is no longer appropriate because continued designation of low-to-moderate risk HPV DNA test devices as class III devices contradicts the current understanding of HPV infection and its relationship to the development of cervical cancer. Based on new scientific information published in the past 15 years, it is now generally agreed that identifying and typing HPV infection does not bear a direct relationship to stratification of the risk for cervical cancer. Most acute infections caused by HPV are self-limiting [1, 4-7]. It is the persistent HPV infection that may act as a tumor promoter in cancer induction [8-11]. Identifying and typing HPV is an important tool for following patients with persistent HPV infection. Repeated sequential transient HPV infections, even when caused by “high-risk” HPVs, are characteristically not associated with high risk of developing squamous intraepithelial lesions, a precursor of cervical cancer.
A woman found to be positive for the same strain (genotype) of HPV on repeated testing is highly likely suffering from a persistent HPV infection and is considered to be at high risk of developing precancerous intraepithelial lesions in the cervix. It is the persistent infection, not the virus, that determines the cancer risk.
The FDA has accepted the above interpretation of current medical science, as reflected in its March 31, 2003 announcement on approval of the Digene HC2 High-Risk HPV DNA Test while making the following public statements on record [I] :
“The FDA today approved expanded use of a laboratory test to detect the presence in women of human papillomavirus (HPV), one of the most common sexually transmitted infections .”
“The HPV DNA test does not test for cancer, but for the HPV viruses that can cause cell changes in the cervix . If left untreated, these changes can eventually lead to cancer in some women.”
“Most women who become infected with HPV are able to eradicate the virus and suffer no apparent long-term consequences to their health . But a few women develop a persistent infection that can eventually lead to pre-cancerous changes in the cervix.”
“. . .most infections are short-lived and not associated with cervical cancer.”
The present regulatory control of all HPV DNA in vitro tests as class III devices should be reviewed and the present classification status of this type of devices should be subjected to reclassification according to 21 CFR §860 .3 (c) to conform with the current interpretation by the FDA of medical science on this subject, in the spirit of the Federal Food, Drug, and Cosmetic Act promulgated by the agency to bring safe and effective new technologies to the market timely in a fashion consistent with the least burdensome principles of the FDAMA of 1997.
I paragraph one I quoted, “Based on new scientific information published in the past 15 years, it is now generally agreed that identifying and typing HPV infection does not bear a direct relationship to stratification of the risk for cervical cancer. Most acute infections caused by HPV are self-limiting [1, 4-7]. It is the persistent HPV infection that may act as a tumor promoter in cancer induction [8-11].”
What we have here is proof that there is scientific evidence that has been published in the past 15 years that states that HPV infection does not bear a direct relationship to the forming of cervical cancer. It also tells us that HPV, if allowed to will be taken care of by our own body’s natural processes. “. . .most infections are short-lived and not associated with cervical cancer.” With this being said, why do we need Gardasil when our own body is more than capable of eradicating HPV? What we need is a government policy to assist women with the cost of getting follow-up tests when persistent HPV infection is present. This would make more sense and our government would save so much money on these types of programs instead of $360 each for the Gardasil vaccination.
The other thing is that the FDA took this to be fact on March 31 of 2003. This is way before the 2006 approval of Gardasil. This just proves to me that the FDA knew that Gardasil was not necessary and that a more sensitive type of testing was all that was required.
Dr. Sin Hang Lee, M.D., felt that he had such a device. When I read this I felt like this Dr. was being stonewalled in getting this device approved appropriately by the FDA because it would show that Gardasil was dangerous and not necessary. That would hurt Merck in its requirement for money to pay for the VIOXX settlements.
History of the HPV DNA Nested PCR Application
On October 30, 2006, the undersigned, Sin Hang Lee, M.D., a practicing pathologist wrote a letter  to Dr. Steven I . Gutman, Director, Office of In Vitro Diagnostic Device Evaluation and Safety (OIVD), Center for Devices and Radiological Health (CDRH), FDA, enclosing the manuscript of a scientific report titled “Human Papillomavirus Genotyping by DNA Sequencing- The Gold Standard HPV Test for Patient Care”  which was submitted to a professional journal to be considered for publication . The purpose of the letter was to inform the FDA that a more sensitive and more specific device is being introduced for detection of HPV in clinical samples and for preparation of materials for HPV genotyping and to request advice and guidance from the agency for making this device available to hospital laboratories at the point of care. With this letter and manuscript, the FDA was informed of the need for a new generation of HPV testing based on new information available because:
1) A sensitive HPV detection device that can provide accurate genotyping information is needed for following patients with persistent infection that is now recognized to be the tumor promoter in cancer induction.
2) A PCR-based HPV detection device with provision for accurate HPV genotyping is more urgently needed now because vaccination with GardasilTM of the women who are already sero-positive and PCR-positive for vaccine-relevant genotypes of HPV has been found to increase the risk of developing high-grade precancerous lesions by 44.6%, according to an FDA VRBPAC Background Document : GardasilTM HPV Quadrivalent Vaccine . May 18, 2006 VRBPAC Meeting. www.fda.izov/ohrms/dockets/ac/06/briefing/2006-4222B3 .
Without a response from Dr . Gutman or from the OIVD, the petitioner submitted a S 10k application (K063649) on December 7, 2006, identifying Hybrid Captures 2(hc2) High-Risk HPV DNA Test (Digene hc2) manufactured by Digene Corporation, 1201 Clopper Road, Gaithersburg, MD 20878 as the predicate device.
A letter dated January 9, 2007 from the FDA in response to the K063649 submission, signed by Sally A. Hojvat, M.Sc., Ph.D., Director, Division of Microbiology Devices, OIVD , stating:
“We have determined that your type of device is classified as a class III device by the approval order for the VRAPAP Human Papillomavirus DNA detection Kit dated December 23, 1988” and “Section 515(a)(2) of the Act requires a class III device to have an approved PMA before it can be legally marketed, unless the device is reclassified.”
On January 18, 2007, the petitioner submitted a Request for Evaluation of Automatic Class III Designation under Section 513(f)(2) of the FDCA (the Act), but was advised by the Office of Device Evaluation on February 22, 2007 to withdraw the 513(f)(2) submission and resubmit this petition under Section 513(f) .
Historically, HPV testing  was introduced to compensate for the poor sensitivity and specificity of the Pap smear cytology often used as a diagnostic tool for borderline precancerous lesions. The only FDA approved Digene Hybrid Capture 2 (HC2) assay is commonly used to determine if a cervicovaginal lavage sample harbors “high-risk” HPVs , as an adjunctive test for evaluation of the cytologically borderline cases [17-19] . However, it is now recognized that persistent infection of a “high-risk” HPV, not the HPV virus itself, is the pivotal promoter in causing cervical precancerous lesions and cancer [7-10] . Most of HPV infections, even caused by “high-risk” genotypes, are transient with normal Pap cytology in sexually active young women [1, 3-6]. In 93% of the initially infected women, the same viral type is not detected upon re-examination four menstrual cycles later . The median duration of positivity detectable by PCR for a specific HPV type in these young women is 168 days . Multiple “high-risk” HPV infections do not constitute a higher risk for the development of cervical neoplasia when compared with single high-risk HPV infection . For the development and maintenance of a high-grade squamous intraepithelial lesion (SIL), the risk is greatest in women positive for the same genotype of HPV on repeated testing [7-9]. Viral load is not a useful parameter to predict high-grade SIL . High-grade SIL is often associated with a viral DNA load lower than that observed in less severely affected cells .
I am going to run some numbers for you. If 93% of the women that are infected receive the Gardasil vaccine it could increase the risk of cervical cancer by 44.6%. Presently, 50,000 women are diagnosed with cervical cancer a year in developed countries. This means if you increase that number by 44.6% you will have 82,956 women that could be at risk of being diagnosed with cervical cancer in the industrial nations of the world. These numbers are staggering. This could mean that 32,956 additional women will have to go through the horrors of cervical cancer. This also means that their families will have to watch as their mother, sister, grandmother, aunt or friend goes through the procedures necessary because of the disease. I would not wish this on my worst enemy.
…PCR-based HPV DNA tests have not been introduced into the clinical laboratories for assisting patient management in the U.S.A. due to the present FDA regulatory control by which this “type of device is classified as a class III device by the approval order for the VIRAPAP Human Papillomavirus DNA detection Kit dated December 23, 1988 [2, 3] . The regulatory arm of the FDA has resorted to invoking an approval order issued before the HPV PCR technology was developed to block all PCR-based HPV DNA detection assays by assigning them a class III status, requiring PMA submission for their approval. The burden put on the industry in fulfilling the requirements for a PMA submission to clear a qualitative HPV DNA detection assay at the FDA is enormous…
Here Dr. Lee is trying to get approval of a new device that is more accurate but in my opinion the FDA is trying to stonewall his efforts and continue with a device that is outdated. Is the FDA trying to tell us that our scientists are so inept that they cannot invent something better in 19 years??? Could this be because Gardasil is the fatted calf of Merck? These are the questions that I have.
As a result, few or no manufacturers are willing to invest in PMA submissions in order to introduce a PCR-based technology for HPV DNA detection. Assigning a class III classification and requiring PMA application for a new HPV DNA detection device can only serve to suffocate new technologies that may compete with the outdated inaccurate FDA-endorsed Digene HC2 assay. The major reason for which the PCR-based HPV DNA detection device should not be classified into its present class III classification is to remove the regulatory roadblock for the FDA to allow the introduction of “safe and effective new technologies to the market quickly” as promulgated in a statement made by former FDA commissioner Mark B McClellan, M .D. Ph.D.
(1) The summary of the current scientific data by the National Cancer Institute (NCI) in its official document labeled Fact Sheet on HPV, reviewed and updated on 06/08/2006 , further supports the conclusions that even the so-called “high-risk” HPV genotypes pose only a low risk to the impairment of human health and that HPV assays are adjunctive or additional in nature to the Pap test and biopsy, the two pivotal in vitro tests to screen and diagnose precancerous cervical conditions. The relevant paragraphs in this NCI document supporting these conclusions are quoted as follows .
“Most HPV infections occur without any symptoms and go away without any treatment over the course of a few years. However, HPV infection sometimes persists for many years, with or without causing cell abnormalities. ”
“Some types of HPV are referred to as “low-risk” viruses because they rarely develop into cancer. HPV types that are more likely to lead to the development of cancer are referred to as “high-risk. ” Both high-risk and low-risk types of HPV can cause the growth of abnormal cells, but generally only the high-risk types of HPV may lead to cancer. Sexually transmitted, high-risk HPVs include types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68, 69, and possibly a few others. These high-risk types of HPV cause growths that are usually flat and nearly invisible, as compared with the warts caused by types HPV-6 and HPV-11 . It is important to note, however, that the majority of high-risk HPV infections go away on their own and do not cause cancer . “
“Having many sexual partners is a risk factor for HPV infection. Although most HPV infections go away on their own without causing any type of abnormality, infection with high-risk HPV types increases the chance that mild abnormalities will progress to more severe abnormalities or cervical cancer. Still, of the women who do develop abnormal cell changes with high-risk types of HPV, only a small percentage would develop cervical cancer if the abnormal cells were not removed. Studies suggest that whether a woman develops cervical cancer depends on a variety of factors acting together with high-risk HPVs . The factors that may increase the risk of cervical cancer in women with HPV infection include smoking and having many children . ”
” What tests are used to screen for and diagnose precancerous cervical conditions? A Pap test is the standard way to check for any cervical cell changes. A Pap test is usually done as part of a gynecologic exam. The U. S. Preventive Services Task Force guidelines recommend that women have a Pap test at least once every 3 years, beginning about 3 years after they begin to have sexual intercourse, but no later than age 21 .
Because the HPV test can detect high-risk types of HPV in cervical cells, the FDA approved this test as a useful addition to the Pap test to help health care providers decide which women with ASC-US need further testing, such as colposcopy and biopsy of any abnormal areas. (Colposcopy is a procedure in which a lighted magnifying instrument called a colposcope is used to examine the vagina and cervix. Biopsy is the removal of a small piece of tissue for diagnosis.) In addition, the HPV test may be a helpful addition to the Pap test for general screening of women age 30 and over . “
Here are some of items of interest from the above statement from the National Cancer Institute.
“Most HPV infections occur without any symptoms and go away without any treatment over the course of a few years” I found this to be interesting because even the National Cancer Institute believes, for the most part, that HPV will just go away. Interesting. Monitoring the HPV seems to be the most evasive way to go. Injecting our bodies with more chemicals will just damage our fragile immune system.
This next item is of significance. Here is a list of “high-risk HPVs include types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68, 69, and possibly a few others.” Gardasil only addresses two, 16 and 18. What about the rest of them? Don’t they count? They are all high-risk types.
This last one is my favorite. “many sexual partners is a risk factor for HPV infection.” Even the National Cancer Institute sees that having many sexual partners is hazardous to your health. Here is another instance of where abstinence is best in preventing disease. Should not our schools be teaching abstinence instead of condom use? My answer is yes! Preventing HPV is a really good reason in my opinion.
What I have quoted above has been taken from the first 27 pages of the document. There are 68 pages to this document and I will inform you about the rest of the contents in a later article. It is a very interesting read.
Here are the definitions to some of the more technical terms.
Stratification — Function: noun Date: circa 1617, 1 a: the act or process of stratifying — Function: verb Inflected Form(s): strat•i•fied; strat•i•fy•ing Etymology: New Latin stratificare, from stratum + Latin -ificare -ify Date: 1661, transitive verb 1: to form, deposit, or arrange in strata
Squamous — Function: adjective 1 a : covered with or consisting of scales b : of, relating to, or being a stratified epithelium that consists at least in its outer layers of small scalelike cells
Intraepithelial– Function: adjective : occurring in or situated among the cells of the epithelium
Epithelium-Function: noun : a membranous cellular tissue that covers a free surface or lines a tube or cavity of an animal body and serves especially to enclose and protect the other parts of the body, to produce secretions and excretions, and to function in assimilation
All definitions were found at the Merriam-Webster website. http://www.merriam-webster.com
Squamous intraepithelial lesion (SIL). This change is considered precancerous. SIL changes are divided into two categories: low-grade SIL and high-grade SIL.
- Low-grade SIL refers to early changes in the size, shape and number of cells on the surface of the cervix. Most of these lesions return to normal on their own without treatment. Others, however, may continue to grow or become increasingly abnormal in other ways and develop into a high-grade lesion.
Other terms for low-grade SIL are mild dysplasia or cervical intraepithelial neoplasia 1 (CIN 1). According to the National Cancer Institute, these precancerous changes occur most often in women ages 25 to 35, but can appear in other age groups, as well.
Generally, your health care professional will recommend a diagnostic test as a follow-up if your test is categorized as low-grade SIL/CIN I, including colposcopy and biopsy.
High-grade SIL. Cells in this category look very different from normal cells and are less likely to return to normal without treatment and more likely to develop into cancer. These abnormal cellular changes are still confined to the surface of the cervix only and still are considered precancerous changes. High-grade SIL is most common in women age 30 to 40, but can occur in other age groups, as well.
Other terms for high-grade SIL are moderate or severe dysplasia (CIN 2 or CIN 3) carcinoma in situ.
Follow up for high-grade SIL/CIN 2 or CIN 3 involves additional procedures, including biopsy, to determine the degree of abnormality and rule out invasive cancer.
Definition is from the Women’s Health Center a feature of Discovery/Health. http://health.discovery.com/centers/womens/womens.html
Please go to http://www.fda.gov/ohrms/dockets/dockets/07p0210/07p-0210-ccp0001-01-vol1.pdf page 60 document page 58 for all the reference material that was used in this report.
I hope that you found the information that I presented today to be most informative in making your decision in regards to being vaccinated with Gardasil.
May your God bless you and you are in my prayers.
Cynthia Janak is a freelance journalist, mother of three, foster mother of one, grandmother of five, business owner, Chamber of Commerce member. Her expertise is as an administrative professional. Her specialties are adoptee and genealogy research and research journalism. Hobbies: Writing prose, crocheting, Conservative Studies, and rehabbing houses. You can contact Cynthia Janak at <!– var email = ‘cj1951’+’@’; document.write(‘‘); //–> cj1951@<font style=”display:none”><NOSPAM></font>ameritech.net <!– document.write(‘‘); //–>
© Copyright 2007 by Cynthia A. Janak
The views expressed by RenewAmerica columnists are their own and do not necessarily reflect the position of Alan Keyes, RenewAmerica, or its affiliates.
FDA: 28 Miscarriages No Reason to Reexamine Gardasil
By Fred Lucas
CNSNews.com Staff Writer
December 06, 2007
(CNSNews.com) – Since June 2006, when the HPV vaccine Gardasil was approved by the Food and Drug Administration, there have been 28 reported cases in which pregnant women miscarried after receiving the vaccine.
Nonetheless, based on the clinical trials done prior to approval of the drug – which indicated that miscarriages among pregnant women given Gardasil were statistically consistent with miscarriages among women given placebos and in the general population – the FDA remains convinced the vaccine is safe and is not further investigating its effect on pregnant women.
In May, a 24-year-old woman suffered a miscarriage, which an investigator in a report issued to the federal government said, “may have been caused by Gardasil because the patient received the injection within 30 days of the pregnancy.”
In July, a 17-year-old girl from Texas was unaware she was pregnant when she got her second dose of Gardasil. She miscarried, but the cause of the miscarriage hasn’t been determined, according to a report.
The reasons for two other miscarriages this year in Florida – one by a 16-year-old and another by a 24-year-old both – are undetermined, according to reports. But it is known that both women had Gardasil vaccinations shortly before the miscarriages.
Gardasil is the vaccine to prevent the Human Papillomavirus (HPV), a sexually transmitted disease and the leading cause of cervical cancer in women. The package insert for Gardasil states there is “no evidence” the vaccine will cause “impaired female fertility or harm the fetus.”
Most of the 28 reports of miscarriage, which were drawn from the Vaccine Adverse Event Reporting System (VAERS), were attributed to “other medical event.” VAERS reports contain raw, unanalyzed data sent by concerned parties to the FDA and the U.S. Centers for Disease Control and Prevention.
The only Gardasil side effect the FDA has expressed concern about is dizziness immediately after the shot, FDA spokeswoman Karen Riley said. “We’ve not seen signals” of a disproportionate problem with Gardasil and pregnant women, she said.
“If you’re pregnant, then it means you’ve been sexually active,” Riley said. “So it would be somewhat dubious to get a vaccine you’re supposed to have before you’re sexually active.”
While there is no conclusive evidence that any health problems have been caused by the vaccine, Judicial Watch, the conservative government watchdog group that obtained the VAERS reports through a lawsuit, is concerned that the FDA is not scrutinizing the vaccine more closely.
Judicial Watch President Tom Fitton said his group wants to know more about the FDA’s approval of Gardasil and monitoring of potential problems with the vaccine, which some states either have or are considering mandating for school girls.
“Merck lobbied for these mandates,” Fitton told Cybercast News Service . “There are moral issues here. But the primary issue is public health and safety. It’s interesting why our government downplays the apparent adverse reactions of Gardasil. Why are drugs with a distinct social agenda getting less scrutiny in the approval process?”
Riley stressed that the numbers concerning the pregnancies must be placed in context.
“Have they (Judicial Watch) compared that to a similar group of young pregnant women of the same age group who haven’t had Gardasil?” Riley said. “There is always a certain percentage of children born with abnormalities among any sampling. The only way to say if there is a causality relationship is to compare one group to see if they have a higher rate than another group.”
A total of 3,461 adverse reactions, including eight deaths, were reported to the government through the VAERS system since the FDA approved the drug.
Reproduction studies were conducted on female rats at doses up to 300 times the human dose, according to Merck. The tests on the lab rats showed no adverse effect on reproduction or pregnancy. However, the company literature on Gardasil said, “It is not known whether Gardasil should be given to pregnant women.”
During Merck’s clinical trials of 2,226 women, half got the Gardasil vaccine, and the other half got a placebo or empty vaccine. In that group, 40 on Gardasil and 41 on the placebo had an adverse event in their pregnancy.
The most common adverse events were conditions that can result in cesarean section or premature labor. The portions between the Gardasil and placebo were comparable, Merck said.
Merck spokeswoman Jennifer Allen said 2 to 3 percent of the women who became pregnant during the clinical trials had children with problems, and roughly 15 percent of those had miscarriages. This, she said, mirrors the general public of pregnant women, regardless of whether they had the vaccine.
Pointing to the fact that VAERS reports are raw data, she said there was little reason to believe a causal relationship existed.
“It’s what you see in the database of the general population,” Allen told Cybercast News Service . “VAERS are passive reports. It’s plausible someone would get the vaccine, leave the doctor’s office and walk into a pole. You could report that and VAERS would accept it.”
Much of the controversy surrounding Gardasil pertains to the fact that three states – Massachusetts, New Jersey, and Virginia – are mandating sixth-grade girls get the vaccine, and other states are considering such a mandate.
The three states included an opt-out provision, which would let parents choose not to have the vaccine administered to their child for religious or other reasons.
Meanwhile, 38 other states this year passed or considered some type of legislation either mandating, funding, or educating the public about the vaccine, according to the National Council of State Legislatures. New Hampshire and Alaska adopted a voluntary program that supplies the vaccine for free to girls between ages 11 and 18 who want it.
Meanwhile, abroad, the British Department of Health approved a national mandate for school girls to get the vaccine.
After the FDA approved Gardasil, the Advisory Committee on Immunization Practices recommended routine vaccinations for girls ages 11 and 12. HPV infects 20 million people in the United States, with about 6.2 million new cases each year, according to the Centers for Disease Control and Prevention. HPV is responsible for nearly 70 percent of cervical cancer cases.
The American College of Pediatrics and the New England Journal of Medicine have voiced opposition to mandating the vaccine.
Why Doctors are Idiots: 150 Years of Disatrous Advice on Children’s Health (satire)
With mandatory vaccines suddenly being forced onto parents by doctors and so-called “health authorities” in places like Maryland, New Jersey and Texas, you might think that doctors being full of bunk is a new phenomenon. But no, it’s nothing new. Doctors have been full of bunk for more than a hundred years! What follows is a short timeline of the nonsense, junk science, negligence and harmful advice peddled by medical doctors over the last 150 years or so: (see the end of this article for serious follow-up comments describing the intent behind this satire piece)
Ignaz Semmelweis, an Austrian-Hungarian obstetrician working in a clinic that delivers babies, is labeled “insane” by his fellow doctors for having the audacity to suggest that doctors should wash their hands between delivering babies. He’s fired from his job, ostracized by the medical community and later dies in an insane asylum and is only vindicated long after his death when it is realized that, indeed, infections are spread from one patient to another by physicians who are too lazy, stubborn or egoistic to simply wash their hands. (A lack of hand washing continues to be the primary reason why MRSA and other superbugs are spread in hospitals today…)
Don’t breastfeed your babies! Use infant formula instead. It’s more “high-tech.” Cow’s milk is obviously healthier for your babies than mother’s milk, right? That’s what the doc says… Result: Tens of millions of mothers stopped breastfeeding their babies, resulting in widespread nutritional deficiencies that impacted those children for life. The pushing of infant formula onto mothers continues today in hospitals across the country which are paid by infant formula manufacturers to give free samples of infant formula to new mothers, hoping they will stop breastfeeding and start buying formula. (Saving grace: A few courageous pediatricians now speak out forcefully about the importance of breastfeeding…)
Smoking while pregnant? No problem. Doctors recommend Camels more than any other cigarette! Result: Massive chemical toxicity of the bodies of newborns. Increased cancer risk, reduced brain development and a lifetime of immune system disorders. (Cigarette ads routinely appeared in the Journal of the American Medical Association for well over a decade.)
Need a new pair of shoes for your kid? Go size ’em up with the fluoroscope X-ray machine at your local shoe store! Never mind the radiation exposure of 20 – 75 rems per minute! See wikipedia article here. Result: Massive increase in cancer among parents and children who visited the shoe stores. Doctors remained silent on this significant health risk for decades while millions were harmed — even after strong evidence pointed to the fact that X-ray radiation caused cancer.
Hey pregnant women, take thalidomide for your cancer! Don’t worry about your unborn children. This chemical is perfectly safe! Result: 10,000 children born with physical deformities. Doctors continued to use infants and pregnant women in pharmaceutical experiments for the next fifty years. See Vaccines and Medical Experiments on Children, Minorities, Woman and Inmates (1845 – 2007).
Feed your children processed foods! White bread is good for them, don’t you know? And monosodium glutamate is perfectly healthy for children, which is why food companies add it to baby food! So is saccharin, hydrogenated oils and sodium nitrite in processed meat. Result: Massive malnutrition, liver damage, and the beginnings of the diabetes and obesity epidemics that would sweep the nation over the next generation.
Place mercury into the mouths of your little children by having their cavities filled with “silver” fillings (made with 40% mercury, a potent neurotoxin). Result: Widespread mercury toxicity in children, resulting in a sharp increase in neurological conditions, including behavioral disorders, infertility and autism. Ignorant, obstinate dentists continue to use mercury fillings today, and the American Dental Association remains in full support of this extremely dangerous heavy metal that results in the mass poisoning of children.
Your kid have a cold? It’s probably because their tonsils need to be removed! Tonsils have no biological function anyway, doctors claimed. Result: Over the last several decades, surgeons have removed tens of millions of tonsils, maiming children with a medically useless procedure that has now been proven virtually worthless. But it sure did raise funds to pay for the luxury German sedans driven by those surgeons!
Microwave all the food you feed children. It’s quick, convenient and perfectly healthy! Result: A massive increase in the consumption of processed, artificially modified and dead foods. The introduction of the microwave correlates nearly perfectly with the explosion of obesity and diabetes in western nations. Most doctors still have nothing negative to say about the use of the microwave.
Does your child have an ear infection? Hammer them with antibiotics. Don’t worry about the fact that antibiotics are useless against ear infections, or that they wipe out your child’s friendly intestinal flora and cause nutritional deficiencies. It’s doctor-recommended, so it must be good, right? Result: Billions of doses of useless antibiotics helped breed a new generation of superbug viruses that have now escaped the hospitals and are infecting the public at large. Antibiotics are useless to stop them, and doctors still have not figured out that you can kill superbugs with colloidal silver or garlic. (A fact that ancient human civilizations knew thousands of years ago…)
Coat your children with sunscreen. The sun is dangerous and has no health benefits whatsoever, didn’t you know? And besides, all those chemicals in sunscreen are perfectly safe. Result: Children are now living with severe vitamin D deficiencies (even rickets!) that greatly increase rates of breast cancer, prostate cancer, osteoporosis, depression, obesity and diabetes. Doctors still don’t recognize the important role of vitamin D in children’s health, and they prescribe drugs to treat the symptoms of disease rather than recommending vitamin D (which would correct the underlying problems and eliminate the need for pharmaceuticals).
Does your baby have a cough? Feed ’em sugared-up, chemically-contaminated cough syrup made by pharmaceutical companies. Don’t worry that it’s never been tested on infants or approved by the FDA. It works, right? It’s doctor-recommended! Result: Over a billion doses of useless, “quack” cough medicine swallowed by infants. The cough syrup hoax was finally blown wide open in 2007 when a few courageous pediatric physicians finally admitted the products have absolutely no medicinal effects and might, in fact, be dangerous for infants and children. The FDA continues to allow their sale, however, since they’re still quite profitable to Big Pharma (even though they don’t work).
Is little Johnny a bit too jazzed up for your comfort level? Don’t worry, psychiatrists have a solution: Street drugs for children! Illegal amphetamines are now legal thanks to the Big Pharma / FDA partnership, and your friendly psych doctor is ready to prescribe Ritalin and antidepressant drugs to your “hyperactive” kids. Result: Widespread school shootings in America. Tens of millions of children suffer stunted physical and mental development — a dangerous side effects that doesn’t emerge until 2007. See http://www.newstarget.com/021944.html
Too posh to push? Don’t worry, your obstetrician will schedule a C-section childbirth appointment and deliver the baby on YOUR schedule instead of Mother Nature’s. It’s more convenient for him, too, because then he can still make his golf game. Don’t worry about the baby: There’s no benefit to vaginal childbirth anyway, right? What better way to welcome your child to the world than with a scalpel! Result: Millions of women subject their children to non-natural child birthing that results in an increased risk of lung disease afflictions as well as psychological birthing trauma lasting a lifetime.
Worried about your child getting an infectious disease? Inject your children with multiple vaccines. It will protect them from infectious disease and may, in fact, protect them from oral sex! (At least that’s what Merck claims.) Besides, there’s nothing wrong with a little mercury, right? Result: Unknown. It’s a great medical experiment now being conducted on the children of America. It’s backed by idiot doctors and gun-toting law enforcement personnel who are ready to arrest parents who resist the vaccination mandates.
Need some food for your baby? Buy Similac (or any other baby formula powder). It’s made with 42.6% corn syrup solids and 10.1% sugar, making it over 50% refined sugars! Marketed with a cuddly teddy bear on the front label and sporting the claim, “Balanced nutrition for older babies,” Similac and other infant formula products are little more than sugar water for babies. Doctors and pediatricians remain silent. There is no outcry. No national scandal. No action by the FDA to protect babies. Some doctors even recommend this stuff! (And stupid parents keep buying it!)
A survey of 1,600 practicing physicians published in the Annals of Internal Medicine reveals that reveals that nearly half of all doctors failed to report an incompetent colleague who posed a risk to the health or safety of a patient. The same survey also revealed that a majority of doctors would send their patients to get expensive imaging work done at an imaging facility in which they held a financial interest, but only 24 percent of doctors said they would reveal that conflict of interest to patients.
Result: Yet more incompetent, dishonest doctors continue to scam customers and harm patients. The scourge of modern medicine continues as corrupt, ignorant and downright incompetent doctors continue to harm millions of expectant mothers, infants, babies and children with their deadly Big Pharma chemicals and disastrous health advice. The reputation of doctors plummets in the minds of the American public, and most patients now turn to the Internet to find answers that their doctors either don’t know or refuse to tell them. The mass exodus of patients away from conventional medicine is now well underway…
Why doctors are still idiots
When it comes to medical idiocy, these examples are just the tip of the iceberg. The same hopelessly outdated medical system that has given us cigarette-promoting doctors, breastfeeding-censoring doctors and superbug-breeding doctors is now claiming your children need yet more chemicals in their bodies in the form of vaccinations!
And, by the way, these doctors are the only people in the world who are right. They’ll tell you so themselves! They are the sole source of all knowledge on anything related to health and medicine, and they’ve now garnered enough political power that they’ve managed to criminalize parents who disagree with their medical dogma.
You know what the difference is between God and doctors?
God doesn’t think he’s a doctor.
These days, instead of doctors simply being full of nonsense, they are suddenly a very real danger to your personal freedom. Before, they were just peddling health nonsense. Now they hold the keys to your freedom and the custody of your children. Refuse to go along with new mandatory vaccination programs in New Jersey, for example, and you can be arrested, imprisoned, charged with a crime and have your children kidnapped by Child Protective Services. How dare you disagree with the High Priests of medical dogma!
Personally, I don’t necessarily mind doctors being full of crap. It’s amusing to watch, and hilarious to document_ But I do mind doctors being full of crap while invoking law enforcement authorities to pull out a Glock, slap a 10-round magazine in the grip, point the barrel to the head of a mother of three children and demand, “Take OUR medicine, or you’ll be arrested.” Which is, of course, essentially what’s happening in New Jersey and Maryland right now. It’s called Gunpoint Medicine, and if you don’t believe me, move to New Jersey, and refuse to have your children vaccinated. It won’t be long before armed men show up at your front door with Child Protective Services standing behind them, ready to grab your kid, toss him into an unmarked van, and have you arrested for “resisting vaccination.” This is not fiction. I couldn’t make this stuff up if I tried. It takes truly evil people to dream up this kind of medical terrorism — the very people who work for Big Pharma and the FDA.
Or maybe I’m wrong about all this. Maybe doctors and health authorities have been full of crap for a hundred years, and now all of a sudden in 2007, they’re instantly right! Maybe they’ve been visited by supernatural, omniscient beings who gave them perfect knowledge (along with a new Merck vaccine) and all they’re doing is running around the country saving little children’s lives for the good of humanity.
Perhaps 2007 is the new Golden Age of children’s health, to be initiated with a mass injection of kiddies with a dozen new toxic mercury injections to “protect” these kids from things that will probably never happen to them. Maybe now, in 2007, organized medicine has reversed all its years of bullsnot and finally found the light! And that light, we’re told, comes in the form of a pill… or a vaccine… or chemotherapy… or whatever they tell you to take next.
Yes, indeed! We’ve been saved by Big Pharma and a brigade of doctors! Hail the FDA! Praise the pharmaceutical giants! Give thanks for mandatory injections! Listen to the doctors and we’ll all be saved!
Quick Note: This satire piece does not mean to imply that ALL doctors are complete idiots when it comes to health. There are exceptions. Many of the outstanding people I know in natural health started as conventional medical doctors (M.D.s). The difference between complete idiot doctors and intelligent doctors is that idiots are not willing to abandon their existing dogmatic beliefs when faced with new, contradictory evidence. Intelligent people, on the other hand, adapt and evolve their ideas when faced with new information or evidence.
Conventional medicine, for the most part, does not want to learn anything new that might challenge its existing status quo dominance over the lives of parents and children. “Innovation is the enemy of the status quo,” and genuine health enhancement (and disease prevention) is the enemy of the entrenched medical industrial complex. Most doctors are complete idiots because they follow a dogmatic, religious-like belief in blatantly outdated junk medical science, even when real world observations and evidence demands the embracing of ideas that overthrow previously protected beliefs and career egos.
Until doctors can abandon their egos and admit they don’t know everything, they will continue to be full of crap.
The purpose behind this satire piece is not to engage in silly name-calling exercises, but rather to play an important role in social commentary on the huge failures of modern medicine today. Satire and humor have important functions in any free society: They reveal what’s wrong in a hilarious light, simultaneously entertaining us while encouraging us to challenge our own ideas and, perhaps, come up with new, better solutions for future generations. Political cartoons, stand-up comedians and satire pieces like this one all play a role in getting people to think more carefully about the issues at hand.
Consider this: If modern medicine really worked well, and if doctors were creating wonderful solutions that kept people healthy, then we wouldn’t have much of anything to make fun of! The fact that silly humor and examples of idiotic behavior are so easy to find in conventional medicine today is indicative of the failure of medicine to be effective. Satire “attack” humor carries a sub-text message that says, “We can do better.” We don’t have to suffer under an idiotic system of medicine. We can create a better future based on genuine health freedom, the promotion of disease prevention programs, and the embracing of plant-based medicines that are safe, affordable and highly effective.
Until we get there, poking fun at the hilarious (but sometimes quite harmful and disastrous) failures of conventional medicine is an important way to keep reminding us all how crazy we are to follow this entrenched system of failed medicine. After all, if conventional medicine really worked well, wouldn’t we all be healthy by now?
Finally, I must add that there is idiocy and humor in every industry. Even natural health has its own idiots, too. Every industry has some area that can be improved, and there are always idiots working alongside geniuses and compassionate leaders, no matter where you look (except, perhaps, in politics, where it seems to be almost entirely idiots…). It just seems that conventional medicine has more than its fair share of short-sighted individuals (which I am equating with the term “idiots”). It’s not just the doctors, of course, but the doctors have played a significant role in promoting the dogmatic beliefs that have helped deliver this disastrous failure of a health care system that we all suffer under in America today. Cuba actually has better health care results than America, and that country has virtually none of the technology, pharmaceuticals and insurance programs that we have.
That says a lot right there. To some, it’s downright hilarious. Personally, I can’t help but laugh at the whole system of western medicine. And I plan to keep making fun of it for as long as it continues to produce more health care follies.
by Mike Adams..News Target
Secret Government Database
of Vaccine-Damaged Children
The general public is essentially unaware of the true number of people — mostly children — who have been permanently damaged or killed by vaccines. In fact, most parents would be surprised to learn that the government has a secret computer database filled with several thousand names of disabled and dead babies, children who were healthy and alive just prior to receiving the vaccines. Of course, the medical establishment and federal government don’t readily disclose this information because they know it’s likely to frighten parents into seeking other ways to protect their children. In other words, parents just might think this issue through on their own and decide to reject the shots.
Federal Admission of Vaccine Risks:
In 1986, Congress officially acknowledged the reality of vaccine-caused injuries and death by creating and passing The National Childhood Vaccine Injury Act (Public Law 99-660). The safety reform portion of this law requires doctors to provide parents with information about the benefits and risks of childhood vaccines prior to vaccination, and to report vaccine reactions to federal health officials. Doctors are required by law to report suspected cases of vaccine damage. To simplify and centralize this legal requisite, federal health officials established the Vaccine Adverse Event Reporting System (VAERS) — operated by the Centers for Disease Control and Prevention (CDC), and the Food and Drug Administration (FDA).
Ideally, doctors would abide by this federal law and report adverse events following the administration of a vaccine. However, the FDA recently acknowledged that 90 percent of doctors do not report vaccine reactions. They are choosing to subvert this law by claiming the adverse event was, in their opinion, not related to the shot. In fact, every year between 12,000 and 14,000 reports of adverse reactions to vaccines are made to the FDA (data initially accessible only through the Freedom of Information Act). These figures include hospitalizations, irreversible brain damage, and hundreds of deaths. Considering that these numbers may represent just 10 percent, the true figures could be as high as 140,000 adverse events annually. However, even this figure could be conservative. According to Dr. David Kessler, former head of the Food and Drug Administration, “Only about 1 percent of serious events [adverse drug reactions] are reported to the FDA.” Thus, it is entirely possible that millions of people are adversely affected by mandatory vaccines every year.
Maybe it doesn’t matter that doctors won’t report vaccine reactions, because the federal government won’t investigate them. Government officials claim VAERS was designed to “document” suspected cases of vaccine damage. No attempt is being made to confirm or deny the reports. Parents are not being interviewed, and the vaccines that preceded the severe reactions are not being recalled. Instead, new waves of unsuspecting parents and innocent children are being subjected to the damaging shots.
Who Pays for Compensation?
In order to pay for vaccine injuries and deaths, a surtax is levied on mandated vaccines. When parents elect to have their children vaccinated, a portion of the money they spend on each vaccine goes into a Congressional fund to compensate them if their child is hurt or killed by the shot.
The compensation portion of the law awards up to $250,000 if the individual dies, or millions of dollars to cover lifelong medical bills, pain, and suffering in the case of a living (but brain-damaged) child. To date, more than $1 BILLION has already been paid out for hundreds of injuries and deaths caused by mandated vaccines. Thousands of cases are pending.
Vaccine Injury Compensation Claims do not include private settlements, or the many families that become dependent on public assistance for medical and living expenses because of vaccine injuries. Therefore, taxpayers subsidize vaccine manufacturers and the federal government by paying for their vaccine-liability expenses.
How Are Vaccines Made?
Vaccine production is a disgusting procedure. To begin, one must first acquire the disease germ — a toxic bacterium or a live virus. To make a “live” vaccine, the live virus must be attenuated, or weakened for human use. This is accomplished by serial passage — passing the virus through animal tissue several times to reduce its potency. For example, measles virus is passed through chick embryos, polio virus through monkey kidneys, and the rubella virus through human diploid cells —-the dissected organs of an aborted fetus! “Killed” vaccines are “inactivated” through heat, radiation, or chemicals.
The weakened germ must then be strengthened with adjuvants (antibody boosters) and stabilizers. This is done by adding drugs, antibiotics, and toxic disinfectants to the concoction: neomycin, streptomycin, sodium chloride, sodium hydroxide, aluminum hydroxide, aluminum hydrochloride, sorbitol, hydrolized gelatin, formaldehyde, and thimerosal (a mercury derivative).
Aluminum, formaldehyde, and mercury are extremely toxic substances with a long history of documented hazardous effects. Studies confirm again and again that microscopic doses of these substances can lead to cancer, neurological damage, and death. Yet, each of them may be found in childhood vaccines.
In addition to the deliberately planned additives, unanticipated matter may contaminate the shots. For example, during serial passage of the virus through animal cells, animal RNA and DNA — foreign genetic material — is transferred from one host to another. Because this biological matter is injected directly into the body, researchers say it can change our genetic makeup.
Undetected animal viruses may jump the species barrier as well. This is exactly what happened during the 1950s and 1960s when millions of people were infected with polio vaccines that were contaminated with the SV-40 virus undetected in the monkey organs used to prepare the vaccines. SV-40 (Simian Virus 40 — the 40th such virus detected since researchers began looking), is considered a powerful immunosuppressor and trigger for HIV, the name given to the AIDS virus. It is said to cause a clinical condition similar to AIDS, and has been found in brain tumors, leukemia, and other human cancers as well. Researchers consider it to be a cancer-causing virus.
What happens next, once this foul concoction — live viruses, bacteria, toxic substances, and diseased animal matter — is created? This witch’s brew is forced into the healthy child.
Dr. Robert Mendelsohn often criticized modern medicine for its sanctimonious doctrine. He argued that “doctors are the priests who dispense holy water in the form of inoculations” to ritually initiate our loyalty into the larger medical industry. Dr. Richard Moskowitz agrees: “Vaccines have become sacraments of our faith in biotechnology. Their efficacy and safety are widely seen as self-evident and needing no further proof.”
Others see a link between vaccinations and satanic rituals or witchcraft, where animals are sacrificed and their organs brewed in a hellish concoction of horrid substances: voodoo medicine by 21st century mad scientists. Sadly, our children are their unwilling subjects as society is slowly devoured by their insatiable appetite for human experimentation.
FDA/U.S. GOVERNMENT VACCINE DATABASE (Years 1990-2004)
Every year, the FDA receives thousands of reports of adverse reactions after vaccines. These include brain damage and death. This information is stored in a secret government database and is available through the Freedom of Information Act — or right here from Thinktwice/New Atlantean Press! Serious researchers can now study and analyze 15 years of data — tens of thousands of adverse events filed with the FDA/CDC Vaccine Adverse Event Reporting System (VAERS). You will receive the data on a CD disc. The data is easily read with popular word processors, such as Word and Word Perfect or imported into common database programs such as Borland’s Paradox and Microsoft’s Access or Excel. The information can be filtered, sorted, and analyzed in many ways. Categories include vaccines administered, types of reactions, dates of hospitalization or death, and more. Data from 1990 thru August 2004. Code DB15 (1 CD Disc) $25.
Posted November 30, 2007 | 03:33 PM (EST)Memo to those who wanted the autism-vaccine contretemps to just go away: You lost.
Exactly five years ago, I began research for my book Evidence of Harm, which looked into the possible link between mercury, vaccines and the tsunami of autism that now overwhelms our education system.
Along the way, I have encountered many people — in the government, in medical circles, in the media, on the Internet – who are furious at my attempts to shed light on this controversy, and utterly contemptuous of parents, doctors and anyone else who supports research into the hypothesized link between autism and vaccines.
Many of these people, incredibly, still insist that autism is purely a genetic disorder with no known “cause” and probably no cure. They blithely claim that autism has always been with us, in the same epidemic numbers we see today, (If you’re the parent of a young boy in New Jersey, by the way, you now face 1-in-60 odds of a diagnosis), we just never noticed, or else counted those kids as “quirky,” or possibly retarded.
Even officials at the CDC, who traced an e-coli outbreak to a single patch of California spinach within months, cannot say if autism is actually on the increase or not.
Some experts, however, are beginning to understand that autism is clearly on the rise and, thus, must have an environmental component, coupled with a genetic underpinning. But they insist that vaccines or their ingredients (ie, mercury, live measles virus, aluminum) have nothing to do with the epidemic.
They really, really want this vexing vaccine chatter to cease. But it won’t.
Buried beneath the usual tumultuous headlines of recent days were three tidbits of news that clearly underscore why this raging, sometimes vitriolic debate is not ending any time soon. In fact, all three reveal significant cracks in the federal government’s hitherto impenetrable fortress of denial of any vaccine-autism link whatsoever:
1) The CDC granted nearly $6 million for investigators at five major research centers to study 2,700 children over the next five years, in what the Contra Costa Times called “the largest-ever U.S. study aimed at solving one of the most perplexing mysteries of modern times: the cause of autism.”
Lisa Croen, the study’s principal investigator in California, told the paper that, “What’s become very clear is that autism results from a combination of having a genetic predisposition or genetic susceptibility, plus the added extra exposures from environmental factors or other kinds of lifestyle factors.”
Among the “factors” to be studied are family history, events during pregnancy, maternal medications, parental occupation, ambient pollution around the house, and “a child’s vaccination history,” the paper reported.
Oddly, the study will not look at the mercury-based preservative thimerosal. According to the FDA and the Institute of Medicine, the last batches of thimerosal containing vaccines for infants and immune-globulin given to pregnant women expired in late 2003 (except for the flu shot, which is still given to infants and pregnant women).
The new study will only study children born from September 2003 to August, 2005.
But the question remains, and I think it’s legitimate: If an association between vaccines and autism has been completely “ruled out,” then why are we spending taxpayer dollars to study autistic children’s vaccination history?
2) The Department of Health and Human Services announced the formation of a new federal panel, the “Interagency Autism Coordinating Committee,” which will help set public and private research priorities into the cause and treatment of autism, as mandated by the recently passed Combating Autism Act.
Among those named to the panel by HHS Secretary Mike Leavitt were Lyn Redwood, president of the Coalition for Safe Minds (and chief protagonist in my book), and a leading advocate of the mercury-vaccine-autism connection, and Lee Grossman, president and CEO of the Autism Society of America, another staunch supporter of the hypothesis.
Which again begs the question: If the debate over vaccines and autism is over, then why did the Feds appoint two people to this important new panel who will relentlessly push for more taxpayer dollars going into research of vaccines and autism?
3) Lawyers for the US Justice Department and HHS are conceding an autism case that was to be tried in the so-called federal “Vaccine Court,” (officially known as the Autism Omnibus Proceedings of the US Court of Federal Claims), according to papers filed on the court’s on-line docket.
Nearly 5,000 autism cases are pending in Vaccine Court, though a small number of “test cases” are being tried, in which attorneys for the families attempt to link the symptoms of autism to thimerosal and/or the measles-mumps-rubella vaccine (or MMR, which never contained mercury). It was a pending test case that the government conceded.
According to my source, however, the government is NOT conceding that mercury or vaccines cause autism. “In this case, the DOJ conceded that vaccines significantly aggravated a child’s pre-existing autistic symptoms,” my source said, “but the autism itself was caused by a congenital mitochondrial disorder that is entirely genetic.”
And, the source noted, “By conceding ‘significant aggravation,’ I think DOJ is trying to avoid ever having this case go to hearing on the underlying causation issue.”
In other words, this was likely going to be a slam-dunk, and the Feds knew it. Rather than risk having the case become a “test” for thousands of other claims, it looks like the DOJ opted to fold and pay out damages to the family, without actually admitting that vaccines can cause autism.
This entirely unreported event raises several interesting questions, I think. To begin with, if the federal government has conceded that vaccines can cause “significant aggravation” to the (even preexisting) autism symptoms of even just one child, shouldn’t the public be notified?
And if the government has conceded that this child would be better off today had he or she not been vaccinated — in other words, that vaccines made the symptoms of autism go from bad to worse – couldn’t it be possible that vaccines might also, say, make symptoms go from mild to bad?
And if the government concedes that vaccines aggravated the symptoms of autism in at least one child, shouldn’t parents of children with the disorder be informed of this, and shouldn’t they be allowed to opt out of future vaccinations, on medical grounds, if they wish?
And if the government concedes that vaccines can aggravate the symptoms of autism, then shouldn’t that same government also earmark funds to research how and why that occurs?
And of course, why on earth would parents concede that there is “no evidence of an association between vaccines and autism,” when the government has just conceded that there was an (albeit not causal) association?
Finally, to all those who are going to post comments about the autism rates in California not coming down, following the removal of thimerosal from most vaccines: You are right. The most likely explanation is that thimerosal was not responsible for the autism epidemic. But that does not mean that it never harmed a single child.
And keep in mind that, of the record 1000+ additional autism cases recorded in California last quarter, some 75% of them were children who were six years of age or older, and thus born well within the “thimerosal generation.” There is evidence that many factors could conceivably be keeping the California numbers higher than the national average, including aggressive early intervention and outreach to low-income families, increased immigration from countries that still use thimerosal (and immigrant children who are routinely re-immunized upon arrival) and migration of families from less progressive U.S. states eager for California’s relative public largesse.
And remember that the CDC, wisely, does not conduct autism prevalence studies on children until they reach the age of 8, to account for any late stragglers entering the database. If thimerosal did not come out of vaccines entirely until 2003, then it won’t be until 2011 before kids in that birth cohort are studied by the CDC, so vindicating thimerosal entirely might still be a tad premature.
All that said, thimerosal may well not be a factor in a single case of autism. But what if one day, we discovered it had caused, say, one percent of all cases? With estimates of autism as high as 1.5 million in the country, that would mean 15,000 Americans who were ravaged by thimerosal (not to mention everyone overseas).
But if thimerosal is vindicated, or shown to be a very minor player, then what about other vaccine ingredients? And what about the rather crowded vaccine schedule we now impose upon families of young children? And what about reports of unvaccinated children in Illinois, California and Oregon who appear to have significantly lower rates of autism? Shouldn’t we throw some research dollars into studying them?
You can answer that, no, we shouldn’t, because the vaccine-autism debate is over.
But I am willing to wager that it has only just begun.
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Below is a MSNBC Interview with Robert Kennedy on the Vaccine Autism Coverup