vaccines

vaccines

Safety testing on the INTER-relationship of vaccines has NEVER been done.
The vaccines on the schedule have never been tested together.
Neither the CDC nor FDA can prove that the current schedule is safe.

Simian Virus 40 (SV40):
A Cancer Causing Monkey Virus from FDA-Approved Vaccines

Vaccination Agenda: An Implicit Transhumanism / Dehumanism

Vaccines Did Not Save Us – 2 Centuries Of Official Statistics

Congressional Briefing on the Vaccine Injury Compensation Program

127 Research Papers Supporting the Vaccine/Autism Link

Package Inserts and Manufacturers for some US Licensed Vaccines

Irrefutable Evidence Shows Historical Application of Vaccines
Had No Health Benefit or Impact on Prevention of Infectious Disease

Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration

Peanut Oil Used in Vaccines Since the 1960’s

Federal Court Admits Hepatitis B Vaccine Caused Fatal Auto-Immune Disorder

Radial nerve motor palsy following seasonal influenza vaccination

Effects of diphtheria-tetanus-pertussis or tetanus vaccination on allergies and allergy-related respiratory symptoms among children and adolescents in the United States.

Serological association of measles virus and human
herpesvirus-6 with brain autoantibodies in autism

The Lead Vaccine Developer Comes Clean So She Can “Sleep At Night”

The Biodefense and Pandemic Vaccine and Drug Development Act of 2005 (S. 1873), nicknamed “Bioshield Two” intent is to shortcut safety testing for new vaccines and and to protect vaccine makers and the pharmaceutical industry from legal liability for vaccine injuries.

WHO Manual Directing “Authorities” on How to Respond to Vaccine Deniers in Public

Chronological history of vaccination:

1667 The apparent danger of using animal serums foreign to human beings and animal serums foreign to other animals is reported in medical literature when lambs blood was unsuccessfully used as a human blood transfusion.

1670 Circassian traders introduced inoculation to the Turkish “Ottoman” Empire. Women from the Caucasus, who were in great demand in the Turkish sultan’s harem in Istanbul because of their legendary beauty, were inoculated against smallpox as children in parts of their bodies where scars would not be seen.

1673 Inoculation against smallpox appears in Denmark. It was common knowledge that survivors of smallpox became immune to the disease. As early as 430 BC, survivors of smallpox were called upon to nurse the afflicted. The word “inoculation” is derived from the Latin inoculare, meaning “to graft.” Inoculation referred to the subcutaneous instillation of smallpox virus into nonimmune individuals. The inoculator usually used a lancet wet with fresh matter taken from a ripe pustule of some person who suffered from smallpox. The material was then subcutaneously introduced on the arms or legs of the nonimmune person.

1712 First record of vaccinations for smallpox in France.

1717 In 1715, Lady Mary Montague suffered from an episode of smallpox, which severely disfigured her beautiful face. Innoculation against smallpox instituted in England by Lady Montague after she returns from Turkey, where it was in a popular experimental stage at the time.

1721 In the United States, a Premillennialist named Cotton Mather attempts to introduce a crude form of smallpox vaccination by smearing smallpox pus into scratches in healthy people. Over 220 people are treated during the first six months of experimentation. Only six had no apparent reaction. Mather was bitterly attacked for recommending this practice. Boston, Massachusetts. During the decades following the 1721 epidemic in Boston, variolation became more widespread in the colonies of New England. In 1766, American soldiers under George Washington were unable to take Quebec from the British troops, apparently because of a smallpox epidemic that significantly reduced the number of healthy troops. The British soldiers were all variolated. By 1777, Washington had learned his lesson: all his soldiers were variolated before beginning new military operations.

Charles Maitland was granted the royal license to perform a trial of variolation (new term for inoculation) on six prisoners in Newgate on August 9, 1721. On April 17, 1722, Maitland successfully treated the two daughters of the Princess of Wales. Not surprisingly, the procedure gained general acceptance after this success. Although 2% to 3% of variolated persons died from the disease, became the source of another epidemic, or suffered from diseases (e.g., tuberculosis and syphilis) transmitted by the procedure itself, variolation rapidly gained popularity among the aristocracy of Europe.The case-fatality rate associated with variolation was 10 times lower than that associated with naturally occurring smallpox. In the 1750s more European princes died of smallpox, giving further impetus for the use of variolation.

1722 In Wales, a Dr. Wright refers to inoculation against smallpox in the British Isles as “an ancient practice”. A citizen of Wales, 99 years old, states that innoculation had been known and used during his entire lifetime, and that his mother stated it was common during her life, and that she got smallpox through her “innoculation”.

1723First record of smallpox immunization in Ireland, when a doctor in Dublin inoculates 25 people. Three died, and the custom was briefly abandoned.

1724 First record of vaccination for smallpox in Germany. It soon fell into disfavor due to the number of deaths. Years later, doctors were able to reintroduce it.

1740 Smallpox epidemic in Berlin.

1754 Inoculation for smallpox introduced in Rome. In ancient Greece and Rome there was no inoculation as protection against smallpox – no vaccinantion and no smallpox. These nations were known in antiquity as being famous for their general habits of cleanliness. Smallpox was carried there by those who were inoculated.The practice of inoculation was soon stopped because of the number of deaths it caused. Later, the medical profession would successfully reintroduce it.

1763 Epidemic of smallpox in France wipes out a large part of the population. It was immediately attributed to inoculation, and the practice was prohibited by the French government for five years.

1768 The medical profession in France is successful in re-instituting vaccination for smallpox.

1778 Danish physicians move to open two major vaccination houses in Denmark, by order of the King. In Italy, infants were inoculated by Neapolitan nurses without the knowledge of parents.

1791 Edward Jenner vaccinates his 18 month old son with swine-pox. In 1798 he vaccinates his son with cow-pox. His son will die of tuberculosis at the age of 21.

1796 Edward Jenner in Gloucestershire, England credited with concept of vaccination. Jenner vaccinates an 8 year old boy with smallpox pus. Jenner would vaccinate the boy 20 times. The boy would die from TB at the age of 20.

1798 General vaccine programs against cowpox instituted in the US.

1800 Benjamin Waterhouse at Harvard University re-introduces vaccination in Massachusetts.

1801 First widespread experimentation with vaccines begins.

1802 The British government gives Edward Jenner £10,000 for continued experimentation with “smallpox vaccine.” The paradigm that vaccines provide “lifetime immunity” is abandoned, and the concept of “revaccination” is sanctioned.

1809 Massachusetts encourages its towns to make provision for the vaccination of inhabitants with cow pox vaccines.

1810 The London Medical Observer (Vol.VI, 1810) publishes particulars of “535 cases of smallpox after vaccination, 97 fatal cases of smallpox after vaccination and 150 cases of serious injury from vaccination, ten of whom were medical men.”

1822 The British government advances Edward Jenner another £20,000 for “smallpox vaccine” experimentation. Jenner suppresses reports which indicate his concept is causing more deaths than saving lives.

“Jenner looked upon the whole thing as a superfluity, and he hung up “Surgeon, apothecary,” over his door without any of the qualifications that warranted the assumption. It was not until twenty years after he was in practice that he thought it advisable to get a few letters after his name. Consequently he then communicated with a Scotch University and obtained the degree of Doctor of Medicine for the sum of £15 and nothing more. It is true that a little while before, he had obtained a Fellowship of the Royal Society, but his latest biographer and apologist, Dr. Norman Moore, had to confess that it was obtained by little less than a fraud. A few years after this, rather dissatisfied with the only medical qualification he had obtained, Jenner communicated with the University of Oxford and asked them to grant him their honorary degree of M.D., and after a good many fruitless attempts he got it. Then he sent to the Royal College of Physicians in London to get their diploma, and even presented his Oxford degree as an argument in his favour. But they considered he had had quite enough on the cheap already, and told him distinctly that until he passed the usual examinations they were not going to give him any more.” – Dr Walter Hadwen, 1896

1831 Smallpox epidemic in Wurtemberg, Germany, where 995 vaccinated people succumb to the disease. In Marseilles, France, 2000 vaccinated people are stricken with smallpox.

1853 In England, the Compulsory Vaccination Act . From 1853 to 1860, vaccination reached 75% of the live births and more than 90% of the population.

1855 Compulsory nature of Massachusetts vaccination statute firm, and a pre- condition for school admittance. Statutes created in the belief it would “protect children from smallpox.”

1857 Vaccination in England enforced by fines. Smallpox epidemic begins in England that lasts until 1859. Over 14,000 die.

1860 Encyclopaedia Brittanica (8th Edition) states “nothing is more likely to prove hurtful to the cause of vaccination and render the public careless of securing to themselves its benefits, than the belief that they would require to submit to re-vaccination every 10 to 15 years”. Later, in the 11th edition of the Encyclopaedia Britannica, the policy would change: “it is desirable that vaccination should be repeated at the age of 7 to 10 years, and thereafter at intervals during life”.

1863 Second major epidemic of smallpox in England lasts until 1865. 20,000 die.

1867 Vaccination Act of 1867 in England begins to elicit protest from the population and increase in the number of anti-vaccination groups. It compelled the vaccination of a baby within the first 90 days of its life. Those who objected would be continually badgered by magistrates and fined until the child turned 14. The law was passed on the assurance of medical officials that smallpox vaccinations were safe. Nonpayment of fines for skipping smallpox vaccination result in harsh penalties.

“The fact must also be mentioned that the good rules laid down by the immortal Jenner, in regard to the essential conditions to genuineness and full efficacy of vaccination, have for many years been grossly neglected by the medical profession.

The Purveyor-General in New York kept up as large a stock of good virus as the public dispensaries and private practitioners could supply. In the remote lines of the army there were occasions when an adequate supply of fresh virus could not be obtained as soon as wanted, or there were some occasions when none but deteriorated crusts, or dubious sores which came from inoculation by them, could, for weeks, be obtained.

In the first two years of the war there were 4132 cases of variola and varioloid officially reported to the Medical Bureau; and, in addition to these, there were nearly as many more cases of the disease that were not returned to the Bureau in the lists of the war hospital admissions ; that is, the outbreaks of small-pox in hospitals did not, during that period, enter into the bureau records of the contagion, except in certain fatal cases; again, there were many cases of the disease, fatal and otherwise, among recruits at the temporary depots for the volunteers in the several States, which at that period of the war never were officially returned.

In the course of such thorough vaccinations, we have known a completely pock-marked man exhibit a normal susceptibility to vaccinia.

The total number of official deaths from small-pox in the army in the first two years was 1544.” – Sanitary Memoirs of the War of the Rebellion collected and published bt the United States Sanitary Commission, 1867

1870 Third major smallpox epidemic in England begins and lasts until 1872. Over 44,800 dies.

1871 In Birmingham, England from 1871 to 1874, there were 7,706 cases of smallpox.Out of these, 6,795 had been vaccinated. Select committee of the Privy Council convened to inquire into the Vaccination Act of 1867 (England), as 97.5% of the people who died from smallpox were vaccinated for it.

In Bavaria, Germany, vaccination is compulsory and re-vaccination is commonplace. Out of 30,472 cases of smallpox, 29,429 had been vaccinated.

Worldwide epidemic of smallpox begins. Claims 8 million people worldwide.

1872 Japan institutes compulsory smallpox vaccination. Within 20 years 165,000 smallpox cases manifest themselves.

1872 In England, 87% of infants are vaccinated for smallpox. Over 19,000 die in England and Wales.

1880 Smallpox vaccinations start in the United States.

1884 In England, Dr. Charles Creighton is asked to write an article for the Encyclopedia Britannica on vaccination.After much research internationally, he concludes that vaccination constituted “a gross superstition”. Later, Creighton writes two books, “Cowpox and Vaccinal Syphilis” and “Jenner and Vaccination”. In England, more that 1700 children vaccinated for smallpox die of syphillis.

Dr. Sobatta of the German Army reports on the results of vaccination to the German Vaccination Commission, which subsequently publishes data proving that re-vaccination does not work. Deaths from vaccination are routinely covered up by physicians.

1885 General vaccination program against rabies begins in the United States.

1886 A seven year period begins in Japan where 25,474,370 vaccinations and re-vaccinations are performed in Japan, representing 66% of the entire population of Japan. During that period, there are 165,774 cases of smallpox with 28,979 deaths.

1887 In England, Dr. Edgar M. Crookshank, professor of pathology and bacteriology at Kings College, is asked by the British government to investigate the cowpox outbreak in Wiltshire. The result of the investigation was contained in two volumes of “The History and Pathology of Vaccination”, in which he states that “the credit given to vaccination belongs to sanitation”.

1888 Bacteriological Institute opens in Paris for experimentation with animals and production of vaccines and sera. Other institutes open around the world modeled after the Paris Institute.

Bacteriological Institute in Odessa, Russia tries its hand at a vaccine for anthrax. Over 4500 sheep are vaccinated; 3700 of them die from the vaccination.

“The evidence as to re-vaccination on a large scale comes from the army. According to a competent statistician (A. Vogt), the death rate from smallpox in the German army, in which all recruits are re-vaccinated, was 60 per cent, more than among the civil population of the same age; it was ten times greater among the infantry than among the cavalry, and sixty times more among the Hessians than among the Wurtembergers. The Bavarian contingent, which was re-vaccinated without exception, had five times the death rate from smallpox in the epidemic of 1870-71 that the Bavarian civil population of the same ages had, although re-vaccination is not obligatory among the latter..”- Dr. Charles Creighton M.A., M.D. Encyclopedia Britannica, published in 1888
“Notwithstanding the fact that Prussia was the best re-vaccinated country in Europe, its mortality from smallpox in the epidemic of 1871 was higher (59,839) than in any other northern state. “- Dr. Charles Creighton M.A., M.D. Encyclopedia Britannica, published in 1888

1895 Diptheria vaccination program begins. Over the period lasting until 1907, 63,249 cases of diptheria were treated with anti-toxin. Over 8,900 died, giving a fatality rate of 14%. Over the same period, 11,716 cases were not treated with anti-toxin, of which 703 died, giving a fatality rate of 6%.

1896 Carlo Ruta, a professor at the University of Perugia in Italy, states that “vaccination is a world-wide delusion and an unscientific practice, with consequences measured today with tears and sorrow without end.”

1898 Vaccination Act of 1898 in England. Elections held for the “board of guardians”, the administrators of the vaccination laws, and by 1898 over 600 boards in England were pledged not to enforce the law. The Act of 1898 contained the first “conscience clause”, although no claims of conscience were ever approved by magistrates.

1901 A former milk wagon horse had been used to produce sera containing antibodies to diphtheria toxin. In October of that year, the horse developed tetanus and was killed. Diphtheria toxin serum from the horse, dated September 30, 1901, had been incubating tetanus and was used in vaccination programs. A young girl in St. Louis subsequently died of tetanus. Samples from September 30 were used to fill bottles labeled August 24, 1901. These samples of antitoxin were distributed and caused the deaths of 12 more children.

1902 The Chicago Health Department develops its “vaccination creed”, which states that “true vaccination repeated until it ‘no longer takes’ always prevents smallpox. Nothing else does.” The policy is immediately taken up by the US military.

1905 Eleven states in the US have compulsory vaccination laws; 34 states do not. No states physically force injections on citizens. Vaccination was typically made compulsory without state legislation providing for analysis of its history.

1907 England passes the Vaccination Act of 1907, after the newly elected government comes to power. The act allowed a statutory objection from a parent relative to a child vaccination before the child was four months old.

1909 Massachusetts Senate introduces bill prohibiting compulsory vaccination.

“Cancer was practically unknown until cowpox vaccination began to be introduced. I have seen 200 cases of cancer, and I never saw a case of cancer in an unvaccinated person.” – W.B. Clark, New York Press, January 26, 1909

“Scientific evidence begins to mount that where human lymph is employed in a vaccine, syphilis, leprosy and tuberculosis soon follow. Where calf lymph is employed in the creation of a vaccine, tuberculosis and cancer soon follow.” – Cancer and Vaccination by Esculapius

1911 General vaccination programs against typhoid begin in the United States.

1912 First whooping cough (pertussis) vaccine created by two French bacteriologists, Jules Bordet and Octave Gengou, who wanted to use it in Tunisia. After they grew Pertussis bacteria in large pots, they killed it with heat, mixed it with formaldehyde (used to embalm bodies) and injected it into children.

1914 Dr. C. Killick Millard, Medical Officer of Health (Leicester, England) publishes The Vaccination Question. The city of Leicester, with a population of around 300,000 at the time, had for 30 years abandoned infantile vaccination and yet “miraculously” experienced an “enormous decline” in smallpox mortality. Millard was originally pro-vaccine. Empirical experience with the population of the city of Leicester caused him to change his views. The striking fact that in Leicester, without infantile vaccination, the decline has been greater than in most places, and that throughout the country smallpox has continued to decrease in spite of the falling off in vaccination, should surely be sufficient grounds for legitimate doubt.

“If it can be shown that “sanitation”, thoroughly carried out, is alone sufficient for the effective control of smallpox in this country (as in Leicester), why inflict upon the community universal vaccination with all its inseparable drawbacks? Moreover, what justification can there be any longer for compulsion? It cannot be denied that vaccination causes, in the aggregate, very considerable injury to health, most of it only temporary, but some permanent.” – Dr. C. Killick Millard

“One of the medical profession’s greatest boasts is that it eradicated smallpox through the use of the smallpox vaccine. I myself believed this claim for many years. But it simply isn’t true. One of the worst smallpox epidemics of all time took place in England between 1870 and 1872 – nearly two decades after compulsory vaccination was introduced. After this evidence that smallpox vaccination didn’t work the people of Leicester in the English midlands refused to have the vaccine any more. When the next smallpox epidemic struck in the early 1890s the people of Leicester relied upon good sanitation and a system of quarantine. There was only one death from smallpox in Leicester during that epidemic. In contrast the citizens of other towns (who had been vaccinated) died in vast numbers…Doctors and drug companies may not like it but the truth is that surveillance, quarantine and better living conditions got rid of smallpox – not the smallpox vaccine.” – Dr. Vernon Coleman

The report of Dr. William Farr, (1807 – 1883), Compiler of Statistics of the Registrar General of London and considered to be the first developer of vital statistics, stated: “Smallpox attained its maximum mortality after vaccination was introduced. The mean annual mortality for 10,000 population from 1850 to 1869 was at the rate of 2.04, whereas after compulsory vaccination, in 1871 the death rate was 10.24. In 1872 the death rate was 8.33 and this after the most laudable efforts to extend vaccination by legislative enactments.” The compulsory vaccination law was repealed in 1907. By 1919, England and Wales had become one of the least vaccinated countries and had only 28 deaths from smallpox out of a population of 37.8 million people. According to official figures of the Registrar General of England, 109 children under five years in England and Wales died of smallpox between 1910 and 1933. In that same period 270 died from vaccination. Between 1934 and 1961 not one smallpox death was recorded but 115 children under five years died from smallpox vaccination.

1918 Great influenza epidemic attributed to widespread use of vaccines but this information is suppressed. Encephalitis lethargica, an atypical form of encephalitis, reaches epidemic proportions from 1918 to 1930.

1919 Diptheria vaccinations injure 60 and kill 10 in Texas.

1921 Bacille Calmette-Guerin tuberculosis vaccine developed.

1924 Diptheria vaccinations kill 25 in Bridgewater, Connecticut and 20 in Concord, New Hampshire.

1925 Danish researcher Thorvald Madsen tries a modified Pertussis vaccine during an epidemic in the Faroc Islands. It did not prevent Pertussis.

Doctors at the Paris Academy of Medicine discuss deaths occurring shortly after vaccination in Holland and other European countries.

In England, less than 50% of infants are vaccinated for smallpox. 6 deaths occur.

General vaccine programs against tuberculosis began in the United States.

1927 Diptheria vaccinations injure 37 and kill 5 people in China.

British government appoints a committee to inquire into “vaccine lymph”, as it is noticed that the “glycerinated calf lymph” used in vaccinations causes deaths from “sleepy sickness”. Two London professors bring notice of the problem to the government in 1922. It takes 5 years before the government responds.

Smallpox in England dwindles almost to the vanishing point. Fatality of the unvaccinated cases is less than half of the vaccinated cases.

1928 Cases of post-vaccination encephalitis force creation of two Committees of Investigation in Britain.

12 children in Bundaberg, Australia, died shortly after receiving injections of diphtheria vaccine. An investigation by an Australian Royal Commission, headed by a future Nobel Prize-winning immunologist, found that the vaccine had become contaminated by S. aureus. The bottle containing the vaccine had been stored at room temperature for a week before the vaccines were given.

1930 Max Theiler develops a yellow fever vaccine.

Diptheria vaccinations injure 32 and kill 16 in Columbia.

1931 Roosevelt endorses polio “immune serum”, precursor to vaccines in 1950’s.

1932 Diptheria vaccines injure 171 and kill 1 in Charolles, France.

Research (Young) indicates that neuritis is commonly precipitated following vaccination with anti-tetanus, anti-pneumococcal, and anti-meningitis serums.

1933 Danish researcher Thorvald Madsen discovers the Pertussis vaccine’s ability to kill infants without warning (SID). He reports that two babies vaccinated immediately after birth died in a few minutes.

American researchers report that children react to Pertussis vaccine with fever, convulsions and collapse.

Vaccination programs against Yellow Fever begin in the United States.

Compulsory immunization instituted in Geneva.

Diptheria cases decline in Britain over the period of a year.

1934 “After vaccination was introduced, cases of aseptic meningitis were reported as a separate disease from polio, but such were counted as polio before the vaccine was introduced. The Ministry of Health admitted that the vaccine status of the individual is a guiding factor in diagnosis…If a person who is vaccinated contracts the disease, the disease is simply recorded under a different name…Those who contracted polio after the first inoculation were placed on the non-inoculated list…It’s obvious that this practice of screening statistics, apparently in order to suppress facts unfavourable to immunization, invalidates most of the evidence brought forward by the supporters of immunization.” – Maurice Beddow Bayly, member of the Royal College of Surgeons, LRCP

1938 Fifty-eight British physicians sign a mandate against compulsory immunization in Guernseypoint due to the virtual disappearance of Diptheria in Sweden, a country without Diptheria vaccination. Compulsory immunization instituted in Hungary. Diptheria cases rise 35% by 1940. The idea of “booster shots” arises as a “solution” to poor antibody response in infants and newborns. These become customary in the 1940’s.

1939 Compulsory vaccination in Germany raises diptheria cases from 40,000 to 150,000 and, by 1945, to 250,000.

1941 Louis Sauer of Evanston, Illinois, an avid supporter of mass vaccination, reports that only 27% of a group of 89 babies developed “protective antibodies” when vaccinated at three months of age or less.” Sauer urges that Pertussis vaccination “begin no earlier than seven months” because “most of these infants did not yet possess the power to develop adequate immunity when they were injected so early in life”.

General vaccine program against influenza begins in the US. Infantile paralysis epidemic kills 1200 and cripples more.

Child psychologist LeoKanner observes a new illness appearing in US children, “inborn autistic disturbance of affective contact”. The problem became known as “infantile autism” or simply “autism“. Outstanding features of this new problem: self-absorbed alienation, inability to relate in the ordinary way to people and situations from the very beginning of life, detachment, nervous hostility with strangers, emotional bluntness and isolation, impaired relationships, reading with little or no comprehension and inability to process experience.

Diptheria cases in Nazi occupied France rise to 47,000 after Germans force compulsory vaccination. In nearby Norway, which refused vaccinations, there were 50 cases of Diptheria.

1944 Dr. S.S.Goldwater, the New York Commissioner of Hospitals, pointed out in The Modern Hospital Magazine that measures used to check contagious diseases may permit longer life but not stronger life. “Chronic diseases are growing at such a rate that America may become a nation of invalids.” – Dr. S.S.Goldwater

1945 Japan surrenders twice, followed by US bombing of Hiroshima/Nagasaki and a third and final surrender. The Allies mandate compulsory vaccination in Japan. The first cases of autism follow pertussis vaccine introduction.

1946 Werne and Garrow describe the deaths of identical twins within 24 hours of their second Pertussis shot.

1947 Matthew Brody at the Brooklyn Hospital gives detailed descriptions of two cases of brain damage leading to death in children receiving Pertussis shots.

Charles Posner of the Harvard Medical School Department of Neurology writes, “almost any vaccination can lead to noninfectious inflammatory reaction involving the nervous system. The common denominator consists of vasculopathy that is often associated with demyelination.” (demyelination is the stripping of the insulation away from the nerves).

The British Medical Research Council begins testing 50,000 children in Britain with the Pertussis vaccine. All children tested are more than 14 months old (not newborns). Eight infants had convulsions within 72 hours of the shot, 34 had convulsions within 28 days of the shot. British doctors deny a connection between the vaccine and the convulsions, declaring the tests a success and began administering it to all British children. Despite the fact that none of the tests were conducted on children under 14 months old (newborns and babies), the United States holds the tests in evidence that the vaccine is safe for newborns as young as 6 weeks of age.

1948 Randolph K. Byers and Frederick C. Moll of the Harvard Medical School publish an article describing children who had suffered brain damage after receiving Pertussis vaccine. 15 children reacted violently within 72 hours of a Pertussis vaccination. All the children were normal before the shot. None had ever had a convulsion before. One of the children became blind, deaf, spastic and helpless after being given the Pertussis shot. Out of the 15 children, two died and nine suffered from damage to their nervous system. The findings provided the first clear evidence that the vaccine caused serious neurological complications in children. The research was performed at Childrens Hospital in Boston and published in Pediatrics magazine.

Louis Sauer makes an interesting observation at an AMA meeting where Pertussis vaccination was discussed. Louis Sauer points out that “the neurological damage caused by Pertussis vaccine is the same as the damage caused by Pertussis (whooping cough). (Which is logical, because they use the bacteria in the vaccine). According to Sauer, “a customary prophylactic dose of Pertussis vaccine seems to illicit a chain of nervous system reactions and in some cases irreversable pathological changes in the brain. These findings resemble those encountered in cases of severe whooping cough (Pertussis).”

The vaccine is causing the disease condition!

England bans smallpox vaccine!

1950 The findings of Dr. Sandler in North Carolina are denegrated in the public media, who claims that Sandlers findings are a “myth.” Rockefeller Milk Trust and Coca Cola ramp up marketing to force return to previous levels of sugar and dairy product consumption. Polio levels rise to pre-1949 level.

Professor Pierre LePine, noted scientist at the Pasteur Institute in Paris, is reported in the March 30, 1950 edition of the New York Times, as saying “no more than one injection in 2,000 really prevents polio.”

1952 Formulation of the polio vaccine begins. Tens of millions of doses of polio vaccines produced from virus grown in monkey cells infected with SV-40 (Simian Virus #40).

1953 Pertussis vaccinations in France, Chile, Austria, Holland and the Scandinavian countries are positively correlated with cases of autism. US ignores data.

The Swedish conduct a study on the Pertussis vaccine. Anna L. Annell, a Swedish researcher, writes a major work on Pertussis which indicates that “pertussis vaccine may be associated with the most varying kinds of cerebral complications which may be cortical, subcortical or peripheral.” Encephalitis after vaccination is known to produce the same range of disabilities and impairment. Annel also wrote, “during the past few decades certain of the epidemic children’s diseases, measles in particular, have shown an increased tendency to attack the central nervous system. After the 1920’s a large number of cases involving CNS damage were reported.”

1954 Salk vaccine begins to be given to school children in Philadelphia. General vaccination programs against Polio begin in the United States. Polio rate caused by the vaccine accelerates ten-fold in Massachusetts.

1955 Under the MacArthur regime, every citizen in Japan receives two smallpox vaccinations. (Life magazine Aug 22, 1955).

Georgia State public health officers meet in Atlanta (May 1955) to discuss what was going wrong with the Salk vaccine program . A U.S. Public Health scientist at the meeting told the group that “he was not permitted to disclose what had happened because it would jeopardize the investment of the pharmaceutical firms in the vaccine program.”

Measles death rate has naturally declined, without vaccines, to .03 per 100,000 by 1955.

Despite the skyrocketing cases of vaccine-induced polio, the AMA, NFIP and USPHS claim a reduction of 40-50%. Idaho brings its Salk vaccination program to a halt on July 1, 1955. Utah does the same on July 12, 1955.

Boston Herald newspaper reports on April 18, 1955, features an article labeled “Drug Companies Expecting Big Profit on Salk Vaccine”, which stated. “A spokesman for Parke-Davis, which made 50% of the Salk vaccine, said ‘now that it has been declared safe, we can get back the millions we invested in the development of the Salk vaccine and make a profit out of it. Our company will make over $10 million on Salk vaccine in 1955.” Rhodes and Company, Wall Street brokers specializing in drug securities, estimate that the gross revenue of the six vaccine houses licensed to produce and sell Salk vaccine would be about $60 million, with profits of $20 million.

Washington Bureau of the Detroit Free Press reports, on June 3, 1955, that “The USPHS reported that more children who received Salk shots made by the Wyeth Labs suffered polio than could normally be expected;” 1955 AMA Conference in Atlantic City, New Jersey. Article by James C. Spaulding who covered the conference was published in the AMA Journal, June 19, 1955, “A policy of secrecy and deception has been followed by the National Foundation for Infantile Paralysis and the US Public Health Service in the polio vaccine programs. The nation’s physicians were prevented from learning vital information about the trouble with Salk vaccine. The US Public Health Service had an advisory group made up almost entirely of scientists who were receiving money from the National Foundation of Infantile Paralysis, which was exerting pressure to go ahead with the program even after Salk vaccine was found to be dangerous.”. Spaulding further said, “the Infantile Paralysis Foundation kept secret the fact that live virus was detected in four out of six supposedly “finished and safe” lots of vaccine.”

Reports that doctors on the staff of the National Institutes for Health are avoiding vaccination of their children with the Salk vaccine. After experimenting with 1,200 monkeys, they declared the Salk vaccine worthless as a preventative and a danger to take.

US Surgeon General Scheele admits in a closed session of the AMA that “Salk polio vaccine is hard to make and no batch can be proven safe before given to children”. Despite this fact, the public is told that the vaccine is safe. The government announces that it has the intention to vaccinate 57 million people before August 1955. Surgeon General Scheele (who never practiced medicine a day in his life) goes on public radio saying “I have complete confidence in the Salk vaccine. I urge doctors to continue vaccinations.”

First vaccinated generation become adolescents. Vermont reports a 266% increase in polio and Rhode Island reports 454% increase since vaccinations began in 1954. Massachusetts reports 642% increase in polio since vaccinations began in 1954 with vaccination of 130,000 children. In response, the National Foundation for Infantile Paralysis states that the increase in cases was due to the fact that “no children were vaccinated there.” Massachusetts bans the sale of Salk vaccine. Dr. Graham W. Wilson, director of Britains Public Health Laboratory Service, who knew about the NIH Salk vaccine trials, says “I do not see how any vaccine prepared by Salk’s method can be guaranteed safe.”

1957 Governor Knight of California asks the legislature for $3 million in order to insure vaccination for all those under 40 years old with Salk polio vaccine. The newspapers report that corporate profits from the Salk vaccine will be in excess of $5 billion. (Feb 6, 1957). Governor Knight notes there are 4 million Californians under 40 and signs the bill.

Pertussis vaccination programs exist in all industrialized nations, with the US leading the way. The vaccine is promoted as “risk free”.

1958 World literature now contains 107 cases of severe reaction to Pertussis vaccine (93 of those cases were in the US). At the Fountain Hospital in London, Dr. J.M. Berg analyzed the 107 cases and found that 31 of them showed signs of permanent brain damage. Berg calls attention to the danger of mental retardation as an effect of the Pertussis vaccine and emphasizes that “any suggestion of a neurological reaction to a Pertussis vaccination should be an absolute contraindication to further innoculation.” The United States medical establishment ignores and suppresses the data. American physicians maintain that the damage caused is small compared to “lack of ‘serious’ reactions in children vaccinated.” No data has ever been found to justify a basis for this conclusion.

Verdict of $147,000 rendered against Cutter Laboratories in Calfornia for the crippling of two children with the Salk polio vaccine. Cutter Labs was the only vaccine manufacturer not part of the Rockefeller Trust.

1959 The United States never conducts its own clinical trials on Pertussis vaccine, but instead relies (as it still does today) on data collected by Britain’s Medical Research Council in clinical trials in England in the 1950’s for “proof of vaccine safety and effectiveness in newborns and children.” Interestingly, Britain’s trials on 50,000 British children were performed on children more than 14 months old. None of the children were newborns.

National Institute of Health (NIH) approves licensing of Quadrigen vaccine for children, containing Pertussis, Diptheria, Tetanus and Polio vaccines. The new combination vaccine was found to be highly reactive and was withdrawn from the market in 1968 after parents started filing lawsuits against Parke-Davis for vaccine damaged children.

Pertussis vaccine found to have allergenic effect on animals.

1960 British Medical Journal publishes an article by Swedish vaccine researcher Justus Strom, who stated that the neurological complications from the disease Pertussis are less than that in the Pertussis vaccine. Strom also pointed out that “whooping cough (Pertussis) had changed and had become a milder disease, making it questionable whether universal vaccination against it is justified.”

It is estimated in 1960 that over 1,000,000 children have vaccine-caused disabilities, including learning difficulties and school behavioral problems, behavioral disturbances, allergies, speech difficulties, visual problems, and problems in adjustment and coping.

1962 Immunologist George Williamson Auchinvole Dick spoke out at the British Medical Association annual meeting against the smallpox vaccination program enjoined by the Minister of Health, Enoch Powell. “He (Enoch Powell) is asking for a sacrifice of at least 20 babies a year.” – George Dick

1963 British physician writes that pediatricians had become concerned about the high incidence of unpleasant reactions to the diphtheria-tetanus-pertussis vaccine.

Correlation between SAT score decline and increase in violent crime. The study was by Rimland and Larson. The 1960’s marked the beginning of the decline of the American IQ. Tests given in 1970 showed less capacity than in 1945. {In 1977 a Blue Ribbon Panel was convened to investigate the reason for the drop in the general IQ of the United States. Seventy-nine theories were advanced, but none of them satisfactorily explained the drop in mental capacity of the US population. The idea that vaccines could be part of the problem was not brought up.}

American researcher John F.Enders creates a measles vaccine. Mass innoculations begin. Children vaccinated with killed measles vaccine between 1963 and 1967 develop Atypical Measles Syndrome (AMS). Studies suggest the children’s response to the “wild” measles virus is “altered” and that the severity and persistence of symptoms suggests encephalopathy (brain damage.)

1964 Rimland calls attention to the parallels between autism and the brain injured children described by researchers in the 1930’s and 1940’s.

Child autism shows a rising tide in pediatric clinics in the United States. The increased prevalence of autism in the 1950’s and 1960’s precisely reflected the expansion of mandated vaccination programs during the same decades.

1967 At the Bland-Sutton Institute of Middlesex Hospital in London, George Dick writes, “it has been long known that increasing the number of Pertussis bacteria per dose of vaccine increases the frequency of reactions. It would be surprising if decreasing the size of the infants receiving a particular vaccine did not also increase the reactions.” A violation of a standard axiom in medicine, which matches the size and weight to an amount of substance. (Why are newborns getting the same dosage as an adult?).

General vaccination program for Mumps begins in the United States. 1969 Diptheria outbreak in Chicago. The Chicago Board of Heath reports that 37.5% of the Diptheria cases had been fully vaccinated or showed immunity. 1969 Neurologically defective 4 and 5 year olds begin to appear.

1970Due to the increasingly mild nature of whooping cough (Pertussis), infant deaths cease from naturally acquired Pertussis in Sweden. Deaths associated with vaccine continue. Sweden stops Pertussis vaccination in 1970.

US Dept of Health, Education and Welfare (HEW) reports ” as much as 26% of children receiving rubella (german measles) vaccination in national testing programs developed arthralgia and arthritis. Many had to seek medical attention and some were hospitalized.”

A study by Pittman reveals diphtheria-tetanus-pertussis vaccine can induce hypoglycemia due to increased production of insulin. Study is corroborated in 1978 by Hannick and Cohen and by Hennessen and Quast in West Germany. Result: Pertussis and diphtheria-tetanus-pertussis vaccines can cause diabetes.

1972World Health Organization Bulletin No.47 refers to creation of an immune virus and suggests that a useful way to study the effects would be “to put it into a vaccination program and observe the results”. Curiously the spread of HIV infection in Central Africa coincided precisely with an intense smallpox vaccination campaign. Information on the Central African countries most infected with HIV precisely matches WHO figures indicating the number of people vaccinated in these areas.

1974 Article is written in Britain by Kulenkampff, Schwartzman and Wilson who retrospectively analyze 36 cases of neurological illness at the Hospital for Sick Children in London from 1961 to 1972. All the cases were thought to be attributable to DPT shots. Out of 36 cases, 4 recovered completely, 2 died, and 30 were left mentally retarded or in seizure conditions.

British researcher and immunologist George Williamson Auchinvole Dick estimates that there are 80 cases of severe neurological complications from Pertussis vaccine annually. Over 33% of these children died and another 33% were left with brain damage. George Dick maintains he is not convinced that the community benefit from the vaccine outweighs the damage.

The Association of Parents of Vaccine Damaged Children is formed in Britain, and pressures the government to study adverse reactions to Pertussis vaccine.

1975 Federal Drug Administration Bureau of Biologics concludes that Diptheria vaccine is “not as effective an immunizing agent as might be anticipated.” They admit that Diptheria may occur in vaccinated people, and note that “the permanence of immunity induced by the toxoid is open to question.”

Japan stops using Pertussis vaccine following publicity about vaccine-related deaths.

According to a letter from the British Association for Parents of Vaccine Damaged Children, published in the British Medical Journal of February 1976, “two years ago we started to collect details from parents of serious reactions suffered by their children to immunizations of all kinds. In 65% of the cases referred to us, reactions followed “triple” vaccinations. The children in this group total 182 to date. All are severely brain damaged, some are paralyzed, and 5 have died during the past 18 months. Approximately 60% of reactions (major convulsions, collapse, screaming) happened within 3 days and all within 12 days.

Dr. Jonas Salk, creator of the polio vaccine, says that analysis indicates that the live virus vaccine in use since the 1960’s is the principle, if not sole cause of all polio cases since 1961.

More than 500 people receiving flu vaccinations become paralyzed with Guillain-Barre Syndrome.

After declining steadily since 1922, cases of Pertussis (whooping cough) suddenly begin to rise significantly between 1976 and 1980, during the same time vaccination for Pertussis was increased. The number of reported cases has risen each year since 1977. Reasons are said to be “unclear” why school age children make up the bulk of the cases.

West Germany ends its mass Pertussis immunization program.

1977 The University of Glasgow in Scotland, Department of Community Medicine, Dr. Gordon Stuart, publishes a study analyzing 160 cases of adverse reaction and neurotoxicity following DPT vaccination. In 65 of those cases, reactions to DPT shots included convulsions, hyperactivity , severe mental defect and paralysis. In a stern statement, Stuart says, “it seems likely that most adverse reactions are unreported and/or overlooked.” The British government is pressured by the publicity following the new data about Pertussis and DPT vaccinations.

Jonas Salk again warns that live virus vaccines produce the disease. Corprate interests remain silent and nothing is done.

1978 According to Charlotte Parker of the University of Texas Department of Microbiology, the nature of the organism Bordetella Pertussis means that different lots of vaccine made from the same strains sometimes show different properties. 1978 Immune and auto-immune diseases start to manifest themselves in the population. None of the diseases are new. Most are caused by suppression of the immune system and change in the body environment, promoting pleomorphic changes in organisms which have always been in the body, and resulting pathology. (Pleomorphism: the occurrence of two or more structural forms during a life cycle).

In England, Griffith studies pertussis vaccine reactions in children, noting a case in which a boy experiences brain damage 3 days after vaccination and dies 27 days later due to injection of DPT vaccine. In the United States, the FDA finances and conducts a study at UCLA from January 1, 1978 to December 15, 1979 called “Pertussis Vaccine Project: Rates, Nature and Etiology of Adverse Reactions Associated with DPT Vaccine”. The study, the first significant “attempt” to evaluate reactions to the DPT shot, found a higher incidence of adverse reactions to the DPT shot than any previously reported in any literature. The UCLA-FDA study also found that systemic reactions in the central nervous system were present in 50% of the vaccinations. After studying 16,000 DPT and DT vaccination cases, they conclude that the Pertussis (P) element of the DPT shot was the element causing reactions. They also found that the incidence of all DPT reactions was much higher in the population than had been suspected or reported in any scientific literature.

1979 Two pediatricians in California report brain swelling associated with DPT vaccine administration.

1980 It is estimated that 2 million American children with vaccine-caused disabilities. A 1980 issue of Mutation Research notes that children re-vaccinated against smallpox had “chromosomal aberrations in their white blood cells”, leading to the conclusion that smallpox vaccination is mutagenic (that is, causes mutations).

1981 Dr.John Emsley and co-workers at King’s College in London find that fluoride reacts strongly with the bonds which maintain the normal shapes of proteins in the body. The work is subsequently confirmed by Dr. Steven Edwards and co-workers from the University of California in San Diego, and by Drs. Froede and Wilson from the University of Colorado at Boulder. By distorting the configuration of the body’s own protein, the immune system attacks its own protein, resulting in an autoimmune or allergic response. The director of the Occupational Safety and Health Administration (OSHA) office of carcinogenic identification, Dr. Peter Infante reports in the Current Intelligence Bulletin (CIB) that formaldehyde, a common component of vaccines, has cancer causing potential. Dr. John Higginson, director of the International Agency for Research on Cancer (IARC), requires the concealing of the carcinogenic nature of formaldehyde in vaccines. Britain conducts the National Childhood Encephalopathy Study, and finds that there exists a significant correlation between serious neurological illness and Pertussis vaccination occurring within 7 days of the shot. New England Journal of Medicine (11/26/81) publishes a study showing that tetanus vaccines cause T-cell ratios to drop below normal, with the greatest decrease after two weeks. The altered ratios were found to be similar to those found in AIDS victims.

1982 34th Meeting of the American Academy of Neurology releases a study which is published in Neurology magazine indicating that out of 103 infants who die of Sudden Infant Death Syndrome (SIDS), 66% had been vaccinated with DPT prior to death. Of these, 6.5% died within 12 hours of vaccination, 13% within 24 hours, 26% within 3 days, 37% died within 1 week, 61% died within 2 weeks and 70% had died within 3 weeks. SIDS frequencies have a bimodal peak occurrence at 2 and 4 months of age – the same ages when initial doses of DPT are administered to infants. University School of Medicine at Reno, Nevada. Dr. William Torch. (Note: Later, Japan made a law that children under 2 years old were not to be vaccinated. The result was that Japan no longer has SIDS). First cases of Chronic Fatigue Syndrome/ Epstein Barr reported. Study by Geschwind and Behan on Autism reveals the finding of an association between autism, celiac disease, dyslexia, stuttering, migraine headaches, developmental disabilities and left-handedness (all features of post encephalitic syndrome). The study caused a sensation because the connecting thread among the disparate conditions is the childhood vaccination program.

1985 On May 3, 1985 the Assistant Secretary of Health, Edward Brandt, Jr., M.D, testifies before a Senate Committee, “every year 35,000 children suffer neurological complications because of DPT vaccine.” Book about DPT vaccinations “DPT: A Shot in the Dark” is published, revealing aspects of collusion between government agencies, the medical establishment and the pharmaceutical industry. 1986 In Kansas, 1300 cases of Pertussis reported. Over 1100 had been vaccinated. National Childhood Vaccine Injury Act, administered by the US Claims Court in Washington, DC, recognizes an association between the DPT shot and infantile spasms. The court awards $2 million for a reaction to DPT vaccine. 150 lawsuits pending against DPT vaccine makers. National Health Survey finds that between 1969 and 1981, the prevalence of “activity-limiting chronic conditions” in children increased by 44%, from 2.9 million children to 3.8 million children. Almost all of the increase happened between 1969 and 1975. Most of these conditions are readily associated with post-encephalitic syndrome. Childhood respiratory disease during this period increased 47%, childhood asthma increased 65% (with deaths from asthma increasing), mental and nervous system disorders increased 80%, personality and other non-psychotic disorders (behavior disorders, drug abuse and hyperactivity increased 300%, diseases of the eyes and ears (especially otitis media) rose 120%, and cases of hearing loss in the ears rose 129%. All of these increases were identical in both high and low income groups. Connaught Laboratory, manufacturer of DPT vaccine, changes the product info sheet to warn against “allergies”, “anaphylactic sensitivity” and “some data suggests that fever is more likely to happen in those who have had local reactions, and that local reactions are more likely to occur with increasing numbers of doses of DPT.”

1988 Two scientific studies find that new rubella vaccine introduced in 1979 was found to be the cause of Chronic Fatigue Syndrome (Epstein-Barr virus), an immune disorder first reported in 1982.

Research indicates that 25% of those vaccinated against rubella show no evidence of immunity within five years. In Wyoming, 73% of rubella cases occur in vaccinated children.

According to a New York Times article on Nov 8, 1988, page C-1, it is estimated that adolescence was now lasting until the late 20’s and that this represented evidence of a general developmental delay in a generation.

1990 Health Consciousness magazine features article labeled “Live Virus Vaccines and Genetic Mutation” by H.E.Buttram, M.D, in which it is determined that “the physical invasion of the human body by foreign genetic material may have the immediate effect of permanently weakening the immune system, setting in motion a new era of autoimmune diseases.”

Pediatric neurologist Dr. John H. Menkes, professor emeritus at UCLA, reports on 46 children experiencing neurological adverse reaction within 72 hours of a DPT shot. Over 87% of the children reacted with a seizure, 2 children died and most surviving children became retarded, with 72% having uncontrollable seizure disorders. U.S. Claims Court, as of October 31, 1990, indicates that “several thousand claims for compensation from injuries or death caused by vaccines have already been filed.” National Vaccine Information Center.

Estimated 3 million in US with vaccine-caused disabilities.

1990 The Los Angeles Times on October 10th publishes an article “Brain Cancer on Rise in Elderly”, noting that “brain cancer has increased 500% among elderly Americans.” And “it was once considered that brain tumors reached a peak rate in people in their ’30s, and then would rapidly decline, but it now appears that the incidence continues to increase with age.” In December of 1990, a federal regulation was adopted permitting the FDA to circumvent US and International laws forbidding medical experimentation on unwilling subjects.This regulation permits the FDA to inject American military with unapproved experimental drugs or vaccines without informed consent . The FDA merely needs to deem it “not feasible” to obtain the soldiers permission. See Health Letter, Washington, DC. Public Citizens Health Research Group “400,000 Human Guinea Pigs in the Persian Gulf”, Feb 12, 1991.

1991 Operation Desert Storm. American troops are given experimental vaccines against biological agents. Within months thousands of troops sicken with communicable cancer causing virus. Disease deemed “Gulf War Syndrome”. Government denies responsibility. Over 8,000 troops were vaccinated with Botulism, over 150,000 troops were given anthrax vaccine, and all 500,000 troops were given Pyristigimine, an experimental nerve agent. All drugs were experimental. 1991 New York Times, Mar 17th, 1991 “US Vaccine Plan Uses Welfare Offices” indicates the Federal government has considered denying welfare and nutritional benefits to families who refuse vaccinations. 1991 The “conjugated” Hib vaccine introduced in 1988 is extended for use in infants as young as two months. It becomes mandated in 44 states in the US. 1991 The CDC begins the process of mandating Hepatitis B vaccinations for all infants in the United States. Many infants receive multiple doses from birth. 1991 Second Immunization Conference in Canberra, Australia. Dr. Viera Scheibnerova reports that “vaccination is the single most prevalent and most preventable cause of infant deaths”

The US Public Health Service recommends a child receive the first DPT shot at two months of age, with subsequent shots given at 4,6, and 18 months, and between the ages of 4 and 6. At the same time, Europe, Sweden and several other countries routinely “wait” until after 6 months of age “because of the improved antibody response in babies whose immune systems are more developed.”

1992 American Journal of Epidemiology reports that children die at a rate 8x greater than normal within three days of receiving a diphtheria-tetanus-pertussis shot.

An adjuvant is an agent meant to stimulate the immune system and increase the response to a vaccine. Most often aluminium adjuvants are used, but adjuvants like squalene are also used in some vaccines and more vaccines with squalene and phosphate adjuvants are being tested.

squalene

Squalene is an oil molecule native to the body found throughout the nervous system and the brain. Squalene is also the biochemical precursor to the whole family of steroids. Squalene adjuvants are key ingredients in a whole new generation of vaccines intended for mass immunization around the globe. By injecting squalene adjuvants the immune system is galvanize into attacking the vaccine.

In the 1970s Michael Whitehouse and Frances Beck injected squalene oil combined with other materials into rats and guinea pigs and found that few oils were more effective at causing the animal versions of arthritis and multiple sclerosis. There is a close match between the squalene-induced diseases in animals and those observed in humans injected with this oil: rheumatoid arthritis, multiple sclerosis and systemic lupus erythematosus.

“There are now data in more than two dozen peer-reviewed scientific papers, from ten different laboratories in the US, Europe, Asia and Australia, documenting that squalene-based adjuvants can induce autoimmune diseases in animals – observed in mice, rats, guinea pigs and rabbits. Sweden’s Karolinska Institute has demonstrated that squalene alone can induce the animal version of rheumatoid arthritis. The Polish Academy of Sciences has shown that in animals, squalene alone can produce catastrophic injury to the nervous system and the brain. The University of Florida Medical School has shown that in animals, squalene alone can induce production of antibodies specifically associated with systemic lupus erythematosus.” – Dr. Johnny Lorentzen, Karolinska Institute Sweden

“Squalene contributed to the cascade of reactions called “Gulf War syndrome. (GIs developed) arthritis, fibromyalgia, lymphadenopathy, rashes, photosensitive rashes, malar rashes, chronic fatigue, chronic headaches, abnormal body hair loss, non-healing skin lesions, aphthous ulcers, dizziness, weakness, memory loss, seizures, mood changes, neuropsychiatric problems, anti-thyroid effects, anaemia, elevated ESR (erythrocyte sedimentation rate), systemic lupus erythematosus, multiple sclerosis, ALS, Raynaud’s phenomenon, Sjorgren’s syndrome, chronic diarrhea, night sweats and low-grade fever.” – Micropaleontologist Dr. Viera Scheibner

Eating and digesting squalene isn’t a problem. Injecting squalene into the blood galvanizes the immune system to attack it. Autoimmune disorders occur because the human body identifies the squalene molecules as having breached cellular barriers – they are out-of-place. Once the body has identified the squalene molecule as an enemy a self-destructive cross reaction may take place against the same molecule where it occurs naturally in the body – and where it is critical to the health of the nervous system. Once self-destruction begins, it doesn’t stop as the body keeps making the molecule that the immune system is trained to attack and destroy.

“Human oil adjuvants are the most insidious chemical weapon ever devised. Squalene is a trigger for a real biological weapon – what Soviet researchers called a biological time bomb.” – Gary Matsumoto

From inception, vaccines have always been dangerous enough for some experts to call them biological weapons undermining health, manipulating and crippling the immune system, and creating the possibility of future debilitating diseases.

H1N1

Swine Flu 1976 & Propaganda

“There is no evidence that any vaccine thus far developed is effective in preventing or mitigating any attack of influenza. The producers of these vaccines know that they are worthless, but they go on selling them, anyway.” – J. Anthony Morris, Former Chief Vaccine Control Officer at the US Federal Drug Administration

30 million pounds of antibiotics are used in America each year. Even though 25 million pounds are used in animal husbandry to promote growth, only 2 million pounds of those antibiotics are used for specific infections. 84% of salmonella is resistant to at least one antisalmonella antibiotic. 54% percent of Campylobacter jejuni are resistant to at least one anti-Campylobacter antimicrobial agent.

Smithfield Foods, the world’s largest pork packer and hog producer, operates a massive hog-raising operations Perote, Mexico, in the state of Vera Cruz, where the H1N1 outbreak of 2009 originated. A Smithfield subsidiary, Granjas Carrol, raises 950,000 hogs per year. Residents of Perote claim the outbreak was caused by contamination from pig breeding farms located in the area. A municipal health official stated that preliminary investigations indicated that the disease vector was a type of fly that reproduces in pig waste and that the outbreak was linked to the pig farms. According to community residents the organic and fecal waste produced by Granjas Carrol isn’t adequately treated. Area residents complain of “fetid odors” in the air and water, swarms of flies hovering around waste lagoons and respiratory ailments.

In a study published by BioMed Central in 2010 live H1N1 virus was found in fecal material of children.

“A federal advisory panel said the FDA should move ahead to approve or license the new H1N1 vaccine without waiting to receive data from clinical trials to test its safety and efficacy.” – Nicholas Winning

“Each year the FDA approves seasonal vaccines based on strain changes without new human studies.” – Jennifer Corbett Dooreen

Dr. David Sencer, head of the CDC, confirmed on 60 minutes that the 1976 flu vaccine was never field tested.

In 1976 federal officials vaccinated 40 million Americans for the Swine Flu.

“The untested vaccine during the 1976 swine flu scare resulted in thousands of severely neurologically damaged Americans and about 500 reported deaths. The end result from the 1976 debacle cost the government $3.5 billion in damages, two-thirds were for severe neurological injury and death directly due to the CDC’s vaccination campaign. The new Novartis vaccine, which uses a cell base from dogs, was found to be contaminated with canine-specific bacteria.

The CDC refused to honor CBS’s Freedom of Information request to receive flu infection data for each individual state, the network performed independent outreach to all fifty states to get their statistics. A CBS Investigative Report, published on October 21, 2009 contradicts dramatically the CDC’s public relations blitz. In California, among the approximate 13,000 flu-like cases, 86 percent tested negative for any flu strain. In Florida, out of 8,853 cases, 83 percent were negative. In Georgia and Alaska, only 2.4 percent and 1 percent respectively tested positive for flu virus among all reported flu-like cases.” – Richard Gale and Dr. Gary Null

In 1976 those that experienced severe neurological damage developed Guillain-Barre syndrome, an autoimmune disorder of the nervous system which can cause paralysis. (Remember vaccine manufactures are now federally protected from legal responsibility for death and injury due to vaccination!)

In the late 1980’s a measles-mumps-rubella vaccine was manufactured by Smith Kline & French Laboratories that caused adverse reactions in significant numbers of Japanese. Smith Kline & French Laboratories concerned about adverse reactions demanded indemnity.

Fast forward to 2009. A full year before any reported case of the current alleged H1N1, the major pharmaceutical company, Baxter, filed for a patent for H1N1 vaccine: Baxter Vaccine Patent Application US 2009/0060950 A1. Their application states, “the composition or vaccine comprises more than one antigen…..such as influenza A and influenza B in particular selected from of one or more of the human H1N1, H2N2, H3N2, H5N1, H7N7, H1N2, H9N2, H7N2, H7N3, H10N7 subtypes, of the pig flu H1N1, H1N2, H3N1 and H3N2 subtypes, of the dog or horse flu H7N7, H3N8 subtypes or of the avian H5N1, H7N2, H1N7, H7N3, H13N6, H5N9, H11N6, H3N8, H9N2, H5N2, H4N8, H10N7, H2N2, H8N4, H14N5, H6N5, H12N5 subtypes.”

The application further states, “Suitable adjuvants can be selected from mineral gels, aluminium hydroxide, surface active substances, lysolecithin, pluronic polyols, polyanions or oil emulsions such as water in oil or oil in water, or a combination thereof. Of course the selection of the adjuvant depends on the intended use – toxicity may depend on the destined subject organism and can vary from no toxicity to high toxicity.”

“An influenza vaccine is not working for the majority of influenza-like illnesses because it is only designed to combat influenza viruses. For that reason, the vaccine changes nothing when it comes to the heightened mortality rate during the winter months.” – Dr. Tom Jefferson

“The swine flu pandemic of 2009 became a golden harvest for the giant pharmaceutical makers as they receive samples from the CDC to begin producing possible vaccines as well as so-called antiviral drugs like Tamiflu. Many drugmakers are using techniques of genetic manipulation to produce their new vaccine offerings in a race to market. Under rulings made under the Bush Administration, vaccines can be labeled as “unavoidably unsafe” meaning that when a product is “carefully designed, manufactured and marketed, but is dangerous nonetheless,” it is not a defective product, even though it might cause injury. The US government made available one billion dollars to help big vaccine makers like Sanofi-Aventis and GlaxoSmithKline ready production of new vaccines. Novartis leads the herd with $289 million in federal support, followed by Sanofi Aventis with $191 million and GlaxoSmithKline, which gets $181 million.” – F. William Engdahl

A World Health Organization container of H1N1 virus exploded on a passenger train in Luzon, Switzerland. The Swiss cases of H1N1 originate from the area where the explosion took place. It is illegal to ship pathogenic viruses in this way.

Many vaccines need preservatives to prevent serious adverse effects such as the staphylococcus infection that, in one 1928 incident, killed 12 of 21 children inoculated with a diphtheria vaccine that lacked a preservative. Several preservatives are available, including thimerosal, phenoxyethanol, and formaldehyde.

“Vaccines are supposed to be making us healthier; however, in twenty-five years of nursing I have never seen so many damaged, sick kids. Something very, very wrong is happening to our children.” – Patti White, School nurse

“We are in the midst of an enormous medical hoax, a design and purpose that has yet to unfold completely, that will nevertheless reap huge revenues for the vaccine industrial complex.” – Richard Gale and Dr. Gary Null

The GlaxoSmithKline H1N1 flu vaccine manufacturer called for the withdrawal of the October 2009 Canadian batch of the H1N1 vaccine because it produced serious and immediate anaphylactic reactions in several cases.

Gardasil®

Gardasil Researcher Drops A Bombshell

After Merck won approval for Gardasil® in June 2006 Merck funneled money through Women in Government in a bid to change state laws by making it mandatory for 11 to 12 year old girls to be vaccinated with Merck’s new cervical cancer vaccine. Merck stands to make a fortune off Gardasil® as Merck is charging $360 for the three shot regime. Approximately 2 million American girls would need to be vaccinated yearly, Merck would gross $720 million a year if the Gardasil® vaccine became mandatory. Gardasil® will not block infection with all of the human papilloma virus types that can cause cervical cancer. According to the American Cancer Society 3,700 American women died of cervical cancer in 2002 which is about 3 out of 100,000. (In 2005 11 United States Senators and 30 United States Represenatives owned stock in Merck.)

Merck’s Gardasil® vaccine causes death, collapse and chronic illness in young woman and girls, including a new, never-before described “disease” called Juvenile ALS, a fatal condition in which the nervous system is slowly destroyed while consciousness remains unimpaired. This vaccine increases cervical cancer by 44.7% in women and girls who already have Human Papilloma Virus. More than 150 types of Human Papilloma Virus are acknowledged to exist. Cervical Cancer is easily detected and cured in early stages and is not a major killer of women. Cervical cancer affects about 16 of 100,000 women per year and kills about 9 of 100,000 per year. Gardasil® contains substances which may cause sterility in women receiving it and any protection lasts only a few years, so 9 year olds will probably not be sexually active by the time this protection has worn off.

In Febuary 2007, the Food and Drug Administration notified health care providers that infants have been contracting a serious bowell condition after being given a Merck vaccine to protect against rotavirus.

“Merck is steeped in a well-documented record of criminality. Such actions include, but are not limited to, intentionally hiding the liver-damaging effects of its cholesterol drug, intentionally withholding the release of clinical data that revealed the failures of another cholesterol drug; it has dumped vaccine waste and manufacturing chemicals into water supplies; it opened up offshore banking accounts to avoid paying billions of dollars in U.S. taxes, and it was caught in a huge scheme of scientific fraud when it was discovered that the company used in-house writers to secretly write so-called “independent” studies that were published in peer-reviewed medical journals.” – Dr. Doug Henderson and Dr. Gary Null

According to scientific records, African chimpanzees were used in the manufacture of the HB vaccine during the early 1970s. Additional documents prove that human Hepatitis B viruses cultured in vivo in chimpanzees were returned to humans whose infected blood serum was then pooled to develop four different strains of experimental Hepatitis B vaccine pilot tested between 1970 and 1975 in New York City and central Africa.

In brief, a well documented, theoretically viable, and generally neglected evolutionary route of SIVagm to HIV-1 zoonosis sequentially involves: 1) Polio vaccine recipients worldwide, including gay men in New York, and Black Africans in Central Africa, were exposed to simian viruses including SV40, SFR (Simian Foamy Retroviruses containing reverse transcriptase), SIVagm, and perhaps others from the mid-1950s, through at least the 1960s; Between 1965 and 1970, researchers in NYC “isolated” and then inoculated the MS-2 strain of HB virus into the above cited New York and African HB vaccine study guinea pigs.) Human derived HB viruses, and potentially activated retroviral sequences, were then transferred to chimpanzees, then back again to humans in NYC and central Africa during the development and testing of four genetically altered subtypes of the pre-1975 experimental HB vaccine. HIV-1 progenitor contamination, recombination, and/or transmission risks were likely increased during this process by: a) human incubation for more than a decade of polio vaccine contaminants and recombinants including SV40, SFR, and possibly SIVagm; b) the pooling of infected blood serum donated by hundreds of gay American and Black African polio vaccine recipients who had subsequently received injections with chimpanzee cultured strains of HB virus; c) the biohazardous laboratory conditions and viral containment problems reported by the HB vaccine investigators and their affiliates; and finally 5) The four pooled serum-derived HB vaccines that were administered to thousands of guinea pigs by 1975, primarily gay males in NYC and central African Blacks. This series of events provides the best explanation for an early to mid-1970s “punctuated origin event” most precisely fitting the etiological determinations of the HIV-1/AIDS pandemic.

Simian vacuolating virus 40 or Simian virus 40 is a deoxyribonucleic acid based polyomavirus. SV40 was identified in the injected form of the polio vaccine produced between 1955 and 1961. This is believed to be due to kidney cells from infected monkeys being used to amplify the vaccine virus during production. Both the Sabin vaccine (oral, live virus) and the Salk vaccine (injectable, killed virus) were affected; the technique used to inactivate the polio virus in the Salk vaccine, by means of formaldehyde, did not reliably kill SV40.

When two or more vaccines are mixed together in the same formulation, the two vaccines can interfere. This most frequently occurs with live attenuated vaccines, where one of the vaccine components is more robust than the others and suppresses the growth and immune response to the other components. This phenomenon was first noted in the trivalent Sabin polio vaccine, where the amount of serotype 2 virus in the vaccine had to be reduced to stop it from interfering with the “take” of the serotype 1 and 2 viruses in the vaccine.

The simian foamy virus (SFV), a spumavirus, has been co-speciated with Old World primates for about 30 million years, making them the oldest known vertebrate RNA (ribonucleic acid) or retroviruses.

SIVagm is a lentivirus also a retrovirus. Hepatitis B virus Hepadnavirus family. Hepadnaviruses have very small genomes of partially double-stranded, partially single stranded circular DNA. The genome consists of two strands, a longer negative-sense strand and a shorter and positive-sense strand of variable length. In the virion these strands are arranged such that the two ends of the long strand meet but are not covalently bonded together.

The virus binds to specific receptors on cells and the core particle enters the cell cytoplasm. This is then translocated to the nucleus, where the partially double stranded DNA is ‘repaired’ by the viral polymerase to form a complete circular dsDNA genome (called covalently-closed-circular DNA or cccDNA). The genome then undergoes transcription by the host cell RNA polymerase and the pregenomicRNA (pgRNA) is sent out of the nucleus. The pgRNA is inserted into an assembled viral capsid containing the viral polymerase. Inside this capsid the genome is converted from RNA to pdsDNA through activity of the polymerase as an RNA-dependent-DNA-polymerase and subsequently as an RNAse to eliminate the pgRNA transcript. These new virions either leave the cell to infect others or are immediately dismantled so the new viral genomes can enter the nucleus and magnify the infection. The virions that leave the cell egress through budding. This is a deoxyribonucleic acid virus.

HB viruses replicate through an RNA intermediate form by reverse transcription, and in this respect they are similar to retroviruses.

There is evidence demonstrating that the schizophrenia-associated retrovirus (SZRV) is an auto-immune-causing retrovirus in the Type-D family of retroviruses, e.g., SRV-1 (simian retrovirus type 1), SRV-2 (simian retrovirus type 2), M7 (baboon endogenous retrovirus), SMRV-H (squirrel monkey retrovirus), HTLV (human T-cell leukemia virus) and distantly-related to HIV (human immunodeficiency virus).