The following timeline on the history of virology, bacteriology, mycology and vaccination is extremely long but important for the world to know the truth.
May I suggest before reading further to please watch the following YouTube video entitled, “The Worst Cover-up in the History of the Military.”
And finally, please share this information with everyone you know! It is important for everyone to know the truth about vaccines and their risks!
The story of marine David Fey reads like a crime novel and is typical of all the cases I am personally aware of. It is shocking and sad to think that our soldiers pledging their lives to defend the United States are being used as guinea pigs for unknown vaccinations. It is nothing new because it has been going on for 100’s of years.
Let’s start with a few quotes:
“The most dangerous man to any government is the man who is able to think things out… without regard to the prevailing superstitions and taboos. Almost inevitably he comes to the conclusion that the government he lives under is dishonest, insane, intolerable.”
– H L Mencken
“No country and no people can be free and ignorant at the same time.”
– Thomas Jefferson
“The only safe vaccine is the one that is never used.”
– James Shannon
Former National Institutes of Health (NIH) Director
“I haven’t got a flu shot and I don’t intend to.”
– George W. Bush 2004 Presidential Candidate
“Vaccinations only prove that you can inject someone
with highly acidic toxic poisonous chemicals and that person
hopefully surviving the debilitating side effects, such as multiple
sclerosis, lesions on the brain, paralysis, breakdown of the red
and white blood cells, ulcerations of the liver, lung, kidney, pancreas,
stomach and bowels, seizures and death. Vaccinations provide
zero immunity. True immunity that leads to health and fitness
can only be achieved by making healthy lifestyle and dietary choices.”
– Dr. Robert O. Young
The pH Miracle Living Center
The following is a history of virology, bacteriology, mycology and vaccination that has lead to many of the out-breaks and/or epidemics from the Spanish Flu Epidemic to Polio to HIV/AIDS to the Gulf War Syndrome and now to our latest epidemics of prostate and breast cancer, diabetes, obesity and the rise of autism in children.
Dr. Young has stated that the use of vaccinations, antibiotics and anti-fungals will only poison the body leading to the one sickness and one disease – latent tissue acidosis and then death.
All vaccinations, antibiotics and anti-fungals are the acids of morbid fermentation of plant, animal and human matter and when ingested or injected can only prove that you can poison the body and hopefully live through it.
The day will soon come when scientists will proclaim that the use of vaccinations, antibiotics and anti-fungals are harmful to the human body and should not be used under ANY circumstances.
In the words of Thomas Edison, ‘The Doctor of the Future will give no medicine, but will involve the patient in the proper use of food, fresh air, and exercise.’
The future that Thomas Edison speaks is here and now! Read on to understand and to see the course we have been walking for the last several centuries and how things must change before it is to late.
1798 General vaccine programs against cowpox instituted in the US.
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 ‘re-vaccination’ is sanctioned.
1822 The British government advances Edward Jenner another £20,000 for ‘smallpox vaccine’ experimentation. Jenner suppresses reports which indicate his concept is causing more death than saving lives.
1844 Fredrich Loeffler isolated the diphtheria bacillus from the throats of patients.
1881 Sternberg in his own lab isolated the pneumococcus
1882 Robert Koch isolates the tubercle bacillus
1883 Robert Koch isolates the cholera bacillus.
1883 Max Von Pettenkofer suggested that Koch’s bacteria were only one of the many factors in the causation of cholera. He prepared test tubes thick with lethal cholera bacteria and he and several of his students drank them down with no side affects.
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.
1888 Bacteriological Institute in Odessa, Russia tries its hand at a vaccine for anthrax. Over 4500 sheep are vaccinated; 3,700 of them die from the vaccination.
1909 New York Press, January 26, 1909 publishes a report by W.B. Clark which states, ‘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 un-vaccinated person.’ Scientific evidence begins to mount that where human lymph is employed in a vaccine, syphilis, leprosy and TB soon follow. Where calf lymph is employed in the creation of a vaccine, TB and cancer soon follow. (Cancer and Vaccination by Esculapius).
1911 The head of French Public Health for the French Army said that germs alone were ‘powerless to create an epidemic.’
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.
“Vaccinations, Not a Virus, Is Responsible for Spanish Flu – 1918”
– Dr. Robert O. Young
The pH Miracle Living Center
1933 a British science team to identify the first filterable bacteria in man, yet propaganda says that the virus of Spanish flu killed millions of civilians and soldiers during the pandemic from 1918 to 1920.
Many would have us believe that all those American soldiers who died from non-combatant causes died from Spanish flu. However, U.S. Army records show that seven men died after being vaccinated.
A report from U.S. Secretary of War Henry L Stimson, the deaths were not only verified but also there had been 63 deaths and 28,585 cases of hepatitis reported as a direct result of yellow fever vaccination during only six months of the war. Plus, the yellow fever vaccination was only one of the 14 to 25 shots given to recruits.
1911 vaccinations became a requirement in the U.S. Army. Cases of typhoid and vaccinial diseases increased rapidly, according to Army records.
1917 The death rate from typhoid reached the highest point in the history of the U.S. Army after America entered the war.
In 1917, 19,608 men were admitted into army hospitals due to anti typhoid inoculation and vaccinia, according to a report of the Surgeon-General of the U.S. Army; and this doesn’t take into account others whose symptoms were attributed to other causes. The army doctors knew all these cases of disease and death were due to vaccination and were honest enough to admit it in their medical reports. Army doctors tried to suppress the symptoms of typhoid with a stronger vaccine, however it caused a worse form of typhoid, paratyphoid. They then concocted an even stronger vaccine to suppress the previous one and created an even worse disease–Spanish flu.
After the war, this was one of the vaccines used to protect a panic-stricken world from the soldiers returning from WWI battle fronts infected with dangerous diseases.
The rest is history.
1918 Great influenza epidemic attributed to widespread use of vaccines that killed up to 100 million people.
1921 BCG tuberculosis vaccine developed.
1922 A study by Samuel Torrey Orton connects emotional disturbance with neurological problems. This insight was lost after World War II when psychology, psychiatry and psychoanalysis became popular, breaking the connection. The emotional disturbances caused by vaccines then became financial fodder for the new psych-industries. With the causes suppressed, a new industry was born.
1925 Danish researcher Thorvald Madsen tries a modified Pertussis vaccine during an epidemic in the Faroc Islands. It did not prevent Pertussis. (See 1933).
1925 General vaccine programs against tuberculosis began in the United States.
1927 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.
April, 1930 Eli Lilly, makers of thimerisol, inject the product into 22 people with meningitis who all die. Lilly publishes the “study”, claiming that thimerisol, 50% mercury by weight, is safe.
1930 Max Theiler develops a yellow fever vaccine.
1931 Roosevelt endorses polio ‘immune serum’, precursor to vaccines in 1950’s.
1932 Diptheria vaccines injure 171 and kill 1 in Charolles, France.
1933 Danish researcher Thorvald Madsen discovers the Pertussis vaccines ability to kill infants without warning (SID). He reports that two babies vaccinated immediately after birth died in a few minutes.
1933 American researchers report that children react to Pertussis vaccine with fever, convulsions and collapse.
1936 Pertussis vaccine introduced in the United States. Autism begins to appear in children shortly thereafter.
1936 Diptheria vaccine injures 75 in France.
1943 American vaccine researcher Pearl Kendrick reports that adding a metallic salt seemed to heighten the capacity of the Pertussis vaccine to produce anti-bodies. (Metal salt is an ‘adjuvant’ in this way). Some metallic salts used are those of aluminum (alum). Pearl Kendrick is the researcher that urged that Pertussis vaccine be combined with Diptheria vaccine. Later the Tetanus vaccine was added, producing the nefarious DPT Vaccine.
1943 General vaccine program against influenza begins in the US.
1944 Health Practitioners Journal, June 1944, reports Dr. S.S. Goldwater, the New York Commissioner of Hospitals states ‘as a result of the drugs, vaccines and other suppressive treatments used to check diseases, chronic diseases are growing at such a rate that America may become a nation of invalids.’
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 US Government Pertussis vaccine expert Margaret Pittman and FDA’s Charles Kendrick decide to test Pertussis vaccine by injecting it into the brains of mice and see how many survive.
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.
1947 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).
1947 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 denied 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 & babies), the United States holds the tests in evidence that the vaccine is safe for newborns as young as 6 weeks of age. The testing would continue until 1957.
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. The findings provided the first clear evidence that the vaccine caused the serious neurological complications in children.
1948 Randolph Byes and Frederick Moll of Harvard Medical School validate that severe neurological disorders follow the administration of DPT vaccine. The research was performed at Children’s Hospital in Boston and published in Pediatrics magazine. Nothing was done by physicians to halt the use of DPT vaccine.
1948 A study on Pertussis vaccine reaction is done by Randolph K. Byers and Frederick C. Moll of the Harvard Medical School. They examine 15 children who had 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, 2 died and 9 suffered from damage to their nervous system. Physicians were displeased by these results.
1948 England bans smallpox vaccine.
1948 North Carolina polio cases number 2,498. See 1949.
1948 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 irreversible pathological changes in the brain. These findings resemble those encountered in cases of severe whooping cough (Pertussis).’ In other words, the vaccine is causing the disease condition.
1949 US Public Health Service Division of Biologics Standards establish a national potency test for Pertussis vaccine, and modify it in 1953 to establish potency limits. Despite this, the Pertussis vaccine that is pronounced ‘safe’ still causes minimal brain damage (MBD) in humans.
1951 Theiler wins Nobel for work on yellow fever vaccine.
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). Scientists ‘perform experiments in laboratories to determine the correct doses of antigen and supplementary chemicals to use in the polio
vaccine. (Ironically, since the scientific premise of vaccination is faulty, a ‘correct dose of antigen and chemicals’ does not exist).
1953 At the University of Zurich, Dr. S.Kong of the Pediatric Clinic compiles a list of 82 cases of Pertussis vaccine damage from world literature.
1953 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 disease, 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.
1954 Parke-Davis pharmaceutical company combines the DPT shot with Polio vaccine. The new combination of four vaccines is called Quadrigen. (See 1959).
1954 Reward of $30,000 offered to anyone who proves polio vaccine not a fraud. Not one person was able to claim the reward.
1954 Mrs. Oveta Culp Hobby, Secretary of Health, Education and Welfare, allows a press photo to be taken during a ceremony declaring Salk vaccine safe.
1954 Polio rate caused by the vaccine accelerates ten-fold in Massachusetts.
1954 Eli Lilly company begins renovation of a five-story building in Indianapolis in July 1954 for the production of Salk vaccine. It is in full production by October of
1954. Wyeth, Parke-Davis and others follow suit.
1954 A study on ‘neurologic sequelae of prophylactic innoculation’ summarized state-of-the-art knowledge in noting that the common factor in the pathology of encephalitis from vaccination is ‘anaphlactic hypersensitivity’.
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.’
1955 Measles death rate has naturally declined, without vaccines, to .03 per 100,000 by 1955.
1955 At the University of Illinois School of Medicine, Department of Neurology, Niels Low shows that the EEG of infants is sometimes altered by a DPT shot,concluding that significant cerebral reactions and neurological changes occur.
1955 American Cancer Society advertising circular states ‘cancer will strike one of every four persons now living. More children from 3 to 15 years of age die of cancer than from any other disease.’ (50 years before, cancer was unheard of in children). According to the ACS, they are predicting 6.4 million deaths from cancer, compared with 128,000 in 1933–an increase of 6.2 million cases in 22 years. Vaccination, pesticide use and chemical pollution are the main factors that have increased since 1933.
1955 Despite the sky rocketing cases of vaccine-induced polio, the AMA, NFIP and USPHS claim a reduction of 40-50%.
1955 Idaho brings its Salk vaccination program to a halt on July 1, 1955.
Utah does the same on July 12, 1955.
1955 Boston Herald newspaper reports on April 18, 1955, features an article entitled ‘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 made over $10 million on Salk vaccine in 1955.’
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.
1955 The CIA conducts a biological warfare experiment in the Tampa Bay area in Florida with agents withdrawn from an Army CBW center. A sharp rise in whooping cough (Pertussis) cases occurs, including 12 deaths, following the test.
1955 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 more 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.’
1955 Salk Polio Vaccine again used in the US. Cases of polio skyrocket again in the United States.
1955 Reported that doctors on the staff of the National Institutes for Health are avoiding vaccination of their children with the Salk vaccine, and that after experimenting with 1200 monkeys, they declared the Salk vaccine worthless as a preventative and a danger to take.
1955 First vaccinated generation become adolescents.
1955 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.’
1955 Massachusetts bans the sale of Salk vaccine.’
1955 Dr. Graham W. Wilson, director of Britain’s 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.’
1955 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.
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.’
1956 Seventeen states in the United States reject their government-supplied Salk polio vaccine.
1956 US government appropriates $53.6 million to ‘aid states in providing free vaccine to people under 20 years of age’.
1956 Idaho health director Peterson states that polio only struck vaccinated children in areas where there had been no cases of polio since the preceding autumn. In 90% of the cases, the paralysis occurred in the arm in which the vaccine had been injected.
1956 American Public Health Service announces 168 cases of polio and 6 deaths among those vaccinated. Censorship is then imposed on the reporting of reactions to Salk vaccine.
1956 Oral polio vaccine developed further by Sabin.
1956 The US Public Health Service and the National Foundation for Infantile Paralysis (Rockefeller) put on a drive to ‘sell’ Salk polio vaccine to the public.
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.
1957 Pertussis vaccination programs exist in all industrialized nations, with the US leading the way. The vaccine is promoted as ‘risk free’.
1957 Scientists isolate a series of Simian (monkey) viruses and discover that these same viruses contaminate polio vaccines. SV-40 found in both Sabin and Salk polio vaccines. (made since early ’50s), Information not made public. The same vaccines continued to be used until the early 1960’s.
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 inoculation.’ 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.
1958 Verdict of $147,000 rendered against Cutter Laboratories in California 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.
1959 National Institutes 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.
1959 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.’
1960 General vaccination program for measles begins in the United States.
1960 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.
1961 A senior school medical officer in Northern England, J.M. Hooper, finds that parents are beginning to refuse to bring children for a Pertussis booster shot, based on earlier violent reaction to the ‘vaccination.’ Children were suffering from collapse, vomiting, and uncontrollable screaming. No one paid attention to these warnings.
1961 Sabin polio vaccine immunization campaign.
1963 American researcher John F. Enders creates a measles vaccine. Mass inoculations begin.
1963 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.) See 1967.
1964 Reward of $30,000 offered to prove polio vaccine was not fraud. No takers.
1965 US Government’s leading Pertussis vaccine specialist, Margaret Pittman, (until 1971) states, ‘Bordetella Pertussis is unique among infectious bacteria in its marked ability to modify biological processes.’
1965 Congress passes the Immunization Assistance Act. More states made their vaccination programs mandatory/obligatory.
1967 The FDA stops the use of an experimental cancer vaccine which was producing significant results. Developed by James Rand and Eernest Ayre, a recognized cancer specialist. The Rand vaccine produced significant improvement in terminal patients in over 30% of patients. It cured tumors and breast cancer in four to six months, without radiation, surgery or chemotherapy. The FDA Commissioner was James L. Goddard, the same man who persecuted the use of DMSO. Goddard used the DMSO issue in 1966 in an attempt to foster a medical dictatorship in the US in collusion with the medical and pharmaceutical industries, and remove viable treatments from public access.
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?).
1967 Dr. Vicent Fulginiti, M.D., former chairman of the American Academy of Pediatrics Committee on Infectious Diseases, asserts that inactivated measles vaccine should no longer be administered. See 1963.
1967 Killed measles vaccine is discontinued in the United States.
1967 General vaccination program for Mumps begins in the United States.
1967 Science magazine (10/20/67) features article on Joshua Lederberg of the Department of Genetics, Stanford University School of Medicine. Lederberg notifies the scientific world that ‘live viruses (as in vaccines) are genetic messages used for the purpose of programming human cells’ and ‘we already practice biological engineering on a rather large scale by use of live viruses in mass immunization campaigns’
1970 Due 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.
1970 A study by Pittman reveals Pertussis vaccine can induce hypoglycemia due to increased production of insulin. (Ref: DPT shots). Study is corroborated in 1978 by Hannick and Cohen and by Hennessen and Quast in West Germany. Result: Pertussis and DPT vaccines can cause diabetes.
1972 British Journal of Psychiatry #120 reveals that ‘psychotic disorders may be caused by viral infections.’ (Ref: viruses induced by vaccines).
1972 WHO begins its “Special Programme” in human reproduction with programs for both male fertility control through vaccines and female fertility control.
1972 the World Health Organization (WHO) 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.” It is theorized that WHO used the smallpox vaccination program in Central Africa for this study, since the spread of HIV infection coincides precisely with the most intense and recent smallpox vaccination campaigns. Information on the Central African countries most infected with HIV precisely matches WHO figures indicating the number of people vaccinated in these areas. The virus requested would selectively destroy the T-cell system. (1972 Federation Proceedings of WHO).
1973 The field of genetic engineering is opened by advances in scientific research, making way for creation of recombinant micro-organisms and new viral structures in the laboratory. The U.S. military applies the technology to its chemical and biological weapons program, claiming overtly that such work is ‘to develop defensive vaccines’.
1974 British researcher George Disk 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. Dick maintains he is not convinced that the community benefit from the vaccine outweighs the damage.
1974 The Association of Parents of Vaccine Damaged Children is formed in Britain, & pressures the government to study adverse reactions to Pertussis vaccine.
1974 Henry Kissenger writes a classified “National Security Study Memorandium 2000: Implications of worldwide population growth for U.S. security and overseas interest (NSSM 200)” which identifies India, Bangladesh, Pakistan, Nigeria, Mexico, Indonesia, Brazil, the Philippines, thailand, Egypt, Turkey, Ethiopia and Columbia as targets for initial population reduction. The Philippine Supreme Court found that 3 million Philippians between 12 and 45 years of age were given this vaccine. Native American Woman and Black women in the US received this vaccine. Sterility rates in Native American Women in the US is over 35%. Sterility rates in Black Women in the US is over 25%.
1975 Federal Drug Administration Bureau of Biologics concludes that Diphtheria toxoid (vaccine) is ‘not as effective an immunizing agent as might be anticipated.’ They admit that Diphtheria may occur in vaccinated people, and note that ‘the permanence of immunity induced by the toxoid is open to question.’
1975 Japan stops using Pertussis vaccine following publicity about vaccine-related deaths.
1976 FDA Pertussis vaccine specialist Charles Manclark comments ‘Pertussis vaccine is one of the most troublesome products to produce and assay. It has one of the highest failure rates of all products submitted to the Bureau of Biologics for testing and release. Approximately 15-20% of all lots which pass manufacturer tests fail to pass the tests of the Bureau.’
1976 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.
1976 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.
1976 More than 500 people receiving flu vaccinations become paralyzed with Guilain-Barre Syndrome.
December 1976 No epidemic of Swine flu surfaces despite rapid approval and response to perceived threat following 1 death of a solder at Ft. Dix, NJ. Swine Flu inoculation program shut down after risk of death and polio like syndrome from the vaccination is found to be almost 12 times greater in vaccinated than un-vaccinated people. 5% of people afflicted die, 10% are crippled or maimed for life.
1977 A Blue Ribbon Panel is 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. Y.L. Warten, 1977. (The Prussian education system is also part of the problem, for those volkschuelen).
1977 The British government is pressured by the publicity following the new data about Pertussis and DPT vaccinations.
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 and severe mental defect. In a stern statement, Stuart says, ‘it seems likely that most adverse reactions are unreported and/or overlooked.’
1977 The British government conducts the National Childhood Encephalopathy Study (NCES) which tests the connection between vaccinations and neurological disease.
1977 (Mar) Jonas and Darrell Salk warn live virus vaccines produce same disease.
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 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 results of the study were published in Pediatrics in November.
1978 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 triple vaccine.
1981 The unpublished contractors ‘Final Report’ was submitted to the FDA on March 18, 1980 (a year earlier) and contained revealing data. The study found a higher incidence of adverse reactions to the DPT shot than any previously reported in literature. After the study had run nine months, the FDA convened a Pertussis Symposium, at which it was revealed that ‘the most striking finding in this preliminary analysis is the high frequency of persistent crying, episodes of convulsions and collapse following DPT immunization.’ Because of these findings, the study was curtailed from the planned examination of 50,000 vaccinations to only 17,000. The UCLA FDA study also found that systemic reactions in the central nervous system were present in 50% of the vaccinations. Because of this potentially damaging information, the FDA placed an arbitrary time limit of 48 hours within which reactions had to occur, despite ongoing data which indicates that serious reactions occur after that time limit, in order to limit the statistical data and conceal the extent of the problem from the population. (See 1981).
1985 WHO Vaccines for smallpox and tetanus are laced with female reproductive hormones to induce permanent sterility to “eliminate 150 million excess Sub-Saharan Africans” according to WHO documents.
May 1987 the Times of London reported on its front page that smallpox vaccine administered by the World Health organization had triggered HIV/AIDS. 100 Million vaccinated Africans are at risk. Areas with highest vaccination rate show highest HIV/AIDS rates. Robert Gallo, discoverer of the HIV/AIDS virus, defends those figures and says, “AIDS researchers will keep their mouths shut because they are paid to do so.”
In 1988, an FDA-sponsored follow-up study of the ’18’ children with neurological reactions concluded ‘no significant neurological impairment.’
A 1988 re-examination of those same children by an independent researcher, pediatric neurologist Ronald Gabriel, not associated with the FDA, proved that the FDA lied–only 4 of the 18 were normal. The results were presented at a May 1980 meeting of the Institute of Medicine. Results indicate that encephalopathy is followed by subtle learning, behavioral and neurological problems. (Note: See the book Vaccination, Social Violence and Criminality: the Medical Assault on the American Brain, by Harris Coulter,1990. The FDA is continuously involved in criminal conspiracy and racketeering along with pharmaceutical and chemical companies in the United States.)
1978 Trials of Hepatitis B vaccine in New York City on non-monogamous males between 20 and 40 years old. Homosexuals receive a different vaccine.
1979 Two pediatricians in California report brain swelling associated with DPT vaccine administration.
1979 New rubella vaccine introduced. See 1988.
1979 The US Food and Drug Administration (FDA) funds a study which represents the first significant ‘attempt’ to evaluate reactions to the DPT shot. The study is conducted at the University of California (UCLA) and was published in Pediatrics in
1981. After studying 16,000 DPT and DT vaccination cases, they concluded 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 the scientific literature. Despite these results, even in 1994 physicians promote Pertussis vaccine with confidence, pay little attention to identification of high risk children, and do not carefully observe contraindications. Parents are legally required to vaccinate their children with Pertussis before entering them in school. (See 1982)
1980 Estimated 2 million American children with vaccine-caused disabilities.
1981 At the headquarters of the Occupational Safety and Health Administration (OSHA), the director of the OSHA office of carcinogenic identification, Dr. Peter Infante, pointed out that a Current Intelligence Bulletin (CIB) on formaldehyde was ‘an important document assessing formaldehyde’s cancer causing potential’. The top bureaucracy at OSHA were embarrassed at the release of the truth, and tried to dismiss Infante. On July 27th, Infante writes Dr. John Higginson, director of the International Agency for Research on Cancer (IARC), disagreeing with the IARC decision to conceal the carcinogenic nature of the substance. Formaldehyde is a common component of vaccines.
1981 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. In the US, the FDA limits statistical data to 48 hours in order to conceal damaging data and eliminate data on deaths and damage occurring after that period of time.
1981 Japan begins use of a new childhood Pertussis vaccine, recommended to be given as 4th and 5th dose. US vaccine used for 1st,2nd,3rd doses. 1981 In Britain, Dr. D.L. Miller reports to the NCES on an analysis of the first 1,000 cases of neurological illness. He reported ‘a significant association was shown between serious neurological illness and Pertussis (also DPT) vaccine.’
1981 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 A reporter at WRC-TV in Washington, DC breaks a story on Pertussis vaccine reactions in the documentary ‘DPT: Vaccine Roulette’, which generally informs the American public that their children are at risk from Pertussis vaccinations. (See 1988)
1982 Homosexuals in Chicago, St. Louis, Denver, Los Angeles and San Francisco get Hepatitis B vaccine.
1983 Bellman, Ross and Miller publish a study of 269 cases of infantile spasms which returns to the establishment position that ‘DPT vaccines do not cause infantile spasms, but may trigger their onset in those children in whom the disorder is ‘destined to develop’. (Note: Using this logic, if one can)
1983 Stanford University Study on Pertussis Vaccine. Lawrence Steinman and colleagues at Stanford University School of Medicine perform a study which reveals that children with allergies may overreact to Pertussis vaccine.
1984 – The 1984 Connaught Laboratory package insert for DPT vaccine cites a 1978 Scandinavian study linking the vaccine to the development of hemolytic anemia and warns that this is a contraindication. By 1991, they would remove this warning from their package inserts in order to conceal this data. This kind of anemia is typified by weakness and periodic loss of consciousness.
1984 A complaint was filed by a group of US physicians with the UN Center for Human Rights in Geneva, entitled ‘A Complaint Against Medical Tyranny As Practiced in the United States of America: American Medical Genocide’; the existence of the report was suppressed by the Bush Administration and the media. Reprinted in The Leading Edge in Oct/Nov 1994.
1984 Shaywitz Study at Yale Medical School Pediatrics revealed that ‘minimal brain damage is perhaps the most common and time-consuming problem in current pediatric practice.’
1984 Wyeth Laboratories package insert for DPT vaccine states, ‘The occurrence of Sudden Infant Death Syndrome (SIDS) has been reported following administration of DTP vaccine’ and that ‘approximately 85% of SIDS cases occur in the period 1 through 6 months of age, with the peak incidence at age 2 to 4 months.’
Two years later in 1986, the Wyeth insert stated, ‘SIDS has occurred in infants following administration of DPT’ but went on to state that ‘one study showed that there was no causal connection’. (Note: One wonders who paid for and did that specific study.)
1984 CDC acknowledges that 60% of those receiving hepatitis vaccine are HIV +.
1985 Tests developed to detect simian viruses in vaccines.
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.’ (May 3, 1985).
1985 Hemophilus Influenza type B (HIB) vaccine approved for general use in US. The HIB vaccine is often referred to as the ‘meningitis’ vaccine, but meningitis has several causes.
1986 150 lawsuits pending against DPT vaccine makers.
1986 National Childhood Vaccine Injury Act. Administered by the US Claims Court in Washington, DC, which does recognize an association between the DPT shot and infantile spasms. The court awarded $2 million to a body in 1989 relative to a reaction to DPT vaccine.
1986 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. For the same period of time, levels of disease not associated with vaccine damage remained unchanged.
1986 Connaught Laboratory, manufacturer of DPT vaccine, changes the product info sheet to warn against ‘allergies’ and ‘anaphylactic sensitivity’.
1986 Connaught Laboratories package insert for their DPT vaccine reads ‘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.’
1987 Centers for Disease Control (CDC) releases a study indicating that the Hib vaccine shows an efficacy (effectiveness) rate of 41%. Children were found to be 5 times more likely to contract the disease than those not vaccinated.
1987 66 Japanese victims of Pertussis vaccine receive huge damage awards from the Japanese government.
1988 Lederle Laboratories package insert for DPT vaccine reads ‘Pertussis vaccine has been associated with a greater proportion of adverse reactions than many other childhood vaccinations. Local reactions are common after administration of DTP, occurring in 35-50% of recipients. Febrile [feverish] reactions are more likely to occur in those who have experienced such responses after prior doses.’
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.
1988 Robert S. Mendelsohn M.D, publishes material indicating that Dr. John Seal of the National Institute of Allergy and Infectious Disease believes that ‘any and all flu vaccines are capable of causing Guillain-Barre.’
1988 New ‘conjugated’ [joined together] Hib vaccine approved for use in children at least 18 months old in the United States. Hib = Hemophilus Influenza Type B.
July, 1989 after years of denial, a scientific paper demonstrates conclusively that WHO tetanus vaccines used in the Philippines contained female reproductive hormones, inducing permanent sterility without consent or knowledge of the women treated.
Tetanus toxoid is linked to the human reproductive hormone to overcome immunological tolerance to the hormone and prod the body of the woman into producing antibodies to her own reproductive hormones.
1990 Health Consciousness magazine features article entitled ‘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.’
1990 The US Public Health Service Immunization Practices Advisory Committee (ACIP) and the American Academy of Pediatrics considers high-pitched screaming after a Pertussis (DPT) vaccination an absolute contraindication to further Pertussis vaccine.
1990 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. Menkes conclude, ‘Pertussis vaccine encephalopathy (brain damage) is not a myth but rather a serious complication of immunization.’
1990 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.
1990 Estimated 3 million in US with vaccine-caused disabilities.
1990 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. See 1991 Gulf War Entry.
June 1990, Court case reveals that babies in Los Angeles were used as human guinea pigs with a experimental measles vaccine called Edmonston Zagreb high titer measles vaccine (E-Z ). From 1989-1991, Kaiser Permanente and LA County Dep’t of Health and CDC injected 700+ “mostly minority” babies with unlicensed experimental vaccines with fraudulently-obtained parental consent. E-Z is closely associated with increased death rate in infant girls in Sendgal, Guneau Bisseau, and Haiti before their second birthday. Most of the families are not aware to date that their child was used as a human guinea pig.
1991 Operation Desert Storm. Bush stops war after 100 hours at preserve Iraq as a threat. American troops are given experimental vaccines against biological agents. Within months thousands of troops sicken with the acids that cause cancer. 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 US Public Health Service Advisory Committee on Immunization Practices (ACIP) drafts new guidelines which eliminate most contraindications to Pertussis vaccine. Essentially, this results in a denial or cover-up of most reactions on the grounds that ‘there is no proof the vaccine causes brain ‘ They base their position on several studies financed by vaccine manufacturers conducted in the late 1980’s by vaccine policymakers such as Dr. James Cherry and Dr. Edward Mortimer, who sit on the ACIP Committee and are also paid consultants to US Pertussis vaccine manufacturers, resulting in biased and flawed studies in order to prove ‘no cause and effect’ between the Pertussis vaccine and permanent brain damage. US vaccine policymakers are the CDC and the American Academy of Pediatrics. All this, despite decades of experience indicating the opposite conclusion. (Note: This policy constitutes criminal neglect, racketeering and conspiracy!).
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.
–The Olympian, Nov 23, 1994. Pertussis also can cause Sudden Infant Death.
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.
1992 Lancet, Journal of the British Medical Association, reports (3/7/92) that the oral polio vaccine used in the mid 1970’s to treat recurrent herpes was contaminated with a number of potentially dangerous retroviruses, and may have seeded HIV among Americans’.
1992 Article in the Washington Post, Nov 2, ‘On Vaccinating Safely’ and Dec 14th press release by the National Vaccine Information Center indicate release by the FDA of a report acknowledging more than 17,000 adverse events– including more than 350 deaths–following vaccination, all in a 20 month period ending July 31,
1992. Reported events number far less than actual events, so number is actually larger, perhaps 170,000 or more. 1992 From 1988 to 1992, over $249 million has already been awarded due to hundreds of deaths and injuries caused by mandated vaccines. Thousands of cases are still pending. The permanent injuries from vaccines include, but are not limited to, learning disabilities, seizure disorders, mental retardation, and paralysis. Many of the awards for pertussis vaccine deaths were initially (and wrongfully) misclassified as Sudden Death Syndrome (SIDS).
1992 Centers for Disease Control (CDC) reports that 87% of all cases of polio in the United States between 1973 and 1983 were caused by the vaccine. The CDC also said that every case from 1980 to 1989 was caused by vaccine.
March 19, 1992, Dr. David Heymann, head of the office of research for the World Health Organization’s Global Programme on AIDS, and Harvard pathology professor William Haseltine refuse to discuss the possibility of AIDS transmission via vaccines. Dr. Heymann states in a phone interview from Geneva, “The origin of the AIDS virus is of no importance to science today. Any speculation on how it arose is of no importance.” Haseltine is even more adamant. “It’s distracting, it’s nonproductive, it’s confusing to the public, and I think it’s grossly misleading in terms of getting to the solution of the problem. It’s over, it’s done with, it’s very, very, very unlikely it happened that way, and it’s another nonsense article. It’s the worst kind of reporting as far as I’m concerned.”
1993 Clinton administration announces plans for a National Childhood Vaccination Program. 103rd Congress introduces S732,S733,HR1460, legislation that would attempt to vaccine all children in the United States, while severely limiting exemptions parents could claim. The bills also seek to set up a national vaccine registry to track down parents who resist.
1993 Seattle Times reports that all polio in the US is caused by vaccines. (6/10/93).
1993 The US Army directs Walter Reed Army Institute of Research to sign an agreement with MicroGeneSys in Meridan, Connecticut for a ‘large scale clinical evaluation’ of an AIDS vaccine designed to block destruction of the immune system. The VaxSyn vaccine uses a genetically engineered protein that matches a protein called (gp160) that covers the surface of the HIV virus. (Note: That the HIV virus is harmless and does not ’cause AIDS’ is known, illustrating that the military is in on the AIDS scam). See Duesberg material.
1993 WHO committees more than $356 million on “reproductive health” research. Funding for abortificant (abortion producing) vaccine comes from many sources.
1. $90+ million contributed by Sweden
2. $52+ million contributed by Great Britain
3. $41 million contributed by Norway
4. $27 million contributed by Denmark
5. $12 million contributed by Germany
6. $5.7 million contributed by US
7. $61 million contributed by UNFPA
8. $15.5 million contributed by World Bank
9. $2.5 million contributed by Rockefeller Foundation
10. $1+ million contributed by Ford Foundation
11. $716.5 thousand contributed by IDRC (International Research and Development Centre of Canada)
1994 Researchers at the Gladstone Institute of Virology and Immunology use genetic engineering to alter a Polio virus (Sabin type) to allow it to carry two key genes from the HIV virus, plus proteins from both cholera bacteria and influenza virus, in a misguided attempt to create an ‘AIDS vaccine’ by induction of immune reaction to foreign proteins. (San Francisco Chronicle 9/2/94)
1994 Sweden reports the testing of a ‘new safer Pertussis vaccine’ to combat whooping cough (what is now a relatively mild disease). According to an article in The Olympian, Olympia, Washington, it ‘could be available in the United States, according to federal health officials.’ According to the article ‘the vaccine could mean the end of rare, severe side effects associated with the Pertussis/whooping cough vaccine.’ (Note: On the contrary, the evidence proves the Pertussis organism found in Pertussis ‘vaccine’, whether bred in live tissue (‘live’ virus) or dead tissue (‘killed virus’), causes brain damage and other pathology in humans).
1889 Protégé’s of Louis Pasteur, Emile Rouz & Alexandre Yersin grew a broth thick with diphtheria bacteria and used compressed air to force the broth through a filter of unglazed porcelain.
NO bacteria or solids could pass through the porcelain – only liquid.
They then sterilized the liquid.
They took the sterilized liquid of diphtheria toxin and injected into animals.
The liquid killed the animals not the bacteria!
According to Dr. Young, this early scientific test showed that a liquid toxic acid kills, not a bacteria or fungi. The major contributors to an acidic body that leads to irritation, inflammation, induration, ulceration and degeneration are as follows:
1) Nitric, sulphuric, phosphoric and uric acids from animal proteins including eggs.
2) Lactic acids from dairy products.
3) All sugars including herbal sugars which are all acids including glucose and ethanol alcohol.
4) Vinegar which is diluted acetylaldehyde an acid that destroys brain cells.
5) All mushrooms and algae which break down dead bodies.
6) Peanuts and corn which produce exotoxins and mycotoxins.
7) All fermented foods including soy sauce.
8) Antibiotics which are mycotoxins.
9) Anti-fungals which are stronger mycotoxins.
10) All vaccinations are full of exotoxins and mycotoxins.
1994 Dr. Robert O. Young discovers the pH factor in triggering biological transformation of the red blood cells into bacteria and yeast.
1994 Dr. Robert O. Young discovers that there is only one sickness and one disease and that is the over-acidification of the blood and tissues due to an inverted way of living eating and thinking.
1994 to the present the increase of Autism is at epidemic proportions – 1 in 90 boys and 1 in 150 girls are affected. Dr. Young has suggested that this is a result of congestion of the bowels from eating animal proteins and dairy as well as vaccinations and antibiotics that destroys the root system or intestinal villi of the small intestine – the focal point where new blood is produced.
1994 to the present the increase of breast cancers is now 1 in 3 and the increase of prostate cancers in men is now 1 in 2. Dr. Young has suggested that this is a result of antibiotic and anti-fungal use, vaccination and an acidic lifestyle and diet.
March 1997 zero confirmed “H5N1” human cases exist anywhere in the word. The U.S. Armed Forces Institute of Pathology, Ft. Detrick, Rockville, Maryland, the US research center for biological weaponry, commissions Dr. Jeffery Taubenberger to lead a research team to ISOLATE the 1918 Flu Virus’ genetic code, the most lethal pathogen in history.
Aug. 24, 1997 Brevig, Alaska. Research Team member Johan Hultin sends well-preserved 1918 flu virus specimens (from a frozen body killed by the 1918 flu) to Dr. Taubenberger’s lab in Maryland.
Days later, Taubenberger detects the genetic fragments for which he has been searching. The 1918 virus’ RNA-based gene fragments are analyzed by computer sequencing in order to reveal its complete genetic code. Even with a super-computer, this code sequencing will take years to complete.
April 2000 Observer Newspaper rerports Glaxo, Pfizer, Squibb and Genentec experimented on children at Incarnation Children’s Center, NY. Incarnation Children’s Center is run by Columbia University which was paid to experiment on children, mostly wards of the state minority children. Babies as young as 6 months were injected with double doses of experimental measles vaccine.
Children as young as 4 were given multi-drug cocktails. More than 100 orphans and babies were used in 36 experiments.
November 28, 2002, a rider tacked onto the end of the Homeland Security Bill confers immunity from liability prosecution on Eli Lilly and other manufacturers of vaccines.
October, 2003 Taubenberger’s team finally deciphers the deadly 1918 flu virus’ entire genetic code – completing a 6 year project. Taubenberger’s colleague, R.G. Webster, publishes article in American Scientist Magazine declaring: “The world is teetering on the edge of a flu pandemic that could kill a large fraction of the human population”.
October, 2004 Dmtry Lvov, head of the Russian Virology Institute declares that up to one billion people around the world could die during the next pandemic.
June, 2005 at Mount Sinai School of Medicine in New York (alleged to be Rockefeller controlled), Taubenberger,Peter Palese and Adolfo Garcia-Sastro create plasmids, or DNA rings, from the 1918 killer virus, permanently “stabilizing” its genetic material for use as a biological weapon. This is the final step in revitalizing the deadly pathogen but the press is told tit will only to be used as a “vaccination tool” – even though the disease is currently non-existent.
August, 2005 Taugenberger’s team inserts plasmids into human kidney cells which then transfers human DNA into the virus making it “human specific.” The 1918 virus, responsible for the death of millions around the world is now ready for use by humans
Sept. 9, 2005 the UN in New York City issues a world-wide press release introducing David Nabarro as the “UN System Senior Coordinator for Avian, Human Influenza”.
Sept. 29, 2005 Nabarro issues an “Official U.N. Warning” that “an outbreak of ‘avian influenza’ would kill between 5 million and 150 million people on each continent.”
Oct. 2005 Pres. Bush’s newly appointed secretary of Health and Human Services (HHS, the parent organization of both the CDC and the FDA), former Utah Governor Mike O. Leavitt, intensifies multi-billion Pandemic Bird Flu preparations.
Dec. 2005 Bush solicits Congress for $7.1 Billion to fund “preparations” — $3.3 billion is immediately allocated to Leavitt’s HHS.
January 24, 2006 the Department of Homeland Security awards KBR, a Halliburton subsidiary, a $385 million contract for US detention centers.
Jan. 2006 Leavitt launches website – http://www.pandemicflu.gov – on which he says: “Let me be clear. It is only a matter of time before we discover H5N1 in America. The migration patterns of the wild fowl that carry the virus makes it appearance here almost inevitable!” China hosts the “International Pledging Conference on Avian and Human Influenza” in Beijing and is promised massive sums of money from the west — Leavitt alone commits $334 million in funds to aid China’s research into “vaccine development.” Leavitt has a long history of fostering Chinese trade activities as Utah’s Governor.
March 2006 breaking new ground, Leavitt’s HHS allocates funds to a private television network to produce a “made-for-TV” movie about the “bird flu.” Leavitt jokes that he wants “the handsomest actor” to play his character. Leavitt declares on HHS website (exactly as John D. Rockefeller declared in 1916): “The best defense against influenza is VACCINATION.” Leavitt further declares: “The current U.S. capacity for manufacturing egg-based vaccines is not sufficient to supply our entire population. HHS is supporting research into [human kidney] cell-based vaccine manufacture of producing vaccine domestically.
April, 2006 HHS announces a $97 million contract for the development of cell-based flu vaccine. Leavitt declares: “The FDA can use its Emergency Use Authorization authority to permit the use of unapproved products if there’s a reasonable belief the products may be effective.” 32 states pass laws which make resisting inoculation once ordered by the governor a felony.
These laws join Patriot Act I, II, BARDA, BIOSHIELD I, II in making drug treatment and inoculation mandatory once a Pandemic is called. Unlimited quarantine without review is mandated under these laws for those who resist inoculation under Pandemic conditions. Fully staffed, empty detention centers exist all over North America. The largest, in Alaska, is rumored to have a 2.5 million person capacity.
December, 2006 New York Times reports Gulf War Syndrome positively linked to vaccination of Veterans. More than 100,000 vets contracted the syndrome during the 1991 Desert Storm Operation. More than 20,000 vets have died to date from this syndrome believed to be triggered by squalene, a vaccine “adjuvant.” All modern vaccines contain squalene.
April 17, 2007 The Food and Drug Adminstration (FDA) branch of HHS utilizes its Emergency Use Authorization authority and awards a license to produce H5N1 “Bird Flu” vaccines to Sanofi-Pasteur.
FDA Bird Flu approval letter states: “We have approved your Biologics License Application (BLA) for Influenza Virus Vaccine, H5N1, effective this date. You are hereby authorized to introduce or deliver for introduction into interstate commerce, Influenza Virus Vaccine, H5N1, under your existing Department of Health and Human Services U.S. License No. 1725; however, we acknowledge your statement provided in your submission of April 5, 2007, that Sanofi Pasteur Inc. does not intend to license this product for commercial distribution, since it was produced under contract to the U.S. Department of Health and Human Services as part of national pandemic preparedness initiatives. Influenza Virus Vaccine, H5N1, is indicated for active immunization of persons 18 through 64 years of age at increased risk of exposure to the H5N1 influenza virus subtype contained in the vaccine.” Among the required post-market studies on this untested vaccine are;
1. Protocol submission: Study DMID 04-077: “A randomized, double-blinded, phase I/II, study of the safety, reactogenicity, and immunogenicity of intramuscular inactivated influenza A/H5N1 vaccine in healthy children aged 2 years through 9 years.”
2. Final study report submission: September 30, 2008.Study DMID 04-076: “A randomized double-blinded, placebo-controlled, phase I/II, dose-ranging study of the safety, reactogenicity, and immunogenicity of intramuscular inactivated influenza A/H5N1 vaccine in healthy elderly adults.”
3. Study DMID 05-0043: “Re-vaccination of healthy subjects with intramuscular inactivated subunit influenza A/Vietnam/1203/2004 (H5N1) vaccine representing a drifted variant.
4. “Study DMID 05-0090: “Evaluation of a booster dose of A/Vietnam/1203/04 (H5N1) vaccine administered at 6 months to healthy adult subjects after a two dose schedule at 0 and 1 month.”
5. Study DMID 05-0129: “Open label evaluation of H5N1 vaccine at vaccine manufacturing facilities.”
6. Study DMID 05-0130: “A single center, open label, phase I/II study of the safety and immunogenicity of two 90 µg doses of intramuscular inactivated influenza A/H5N1 vaccine in healthy adult subjects.”
Nov. 26, 2007: Leavitt’s HHS orders 100 million H5N1 “vaccines [doses]” from Sanofi-Pasteur. Expected delivery date, August, 2008. Sanofi-Pasteur issues a press release announcing their lucrative HHS contract (100 million vaccines @ $15 USD each) and declares that the cell-based vaccine will be mass produced in the company’s CHINA facility – then shipped to Stillwater, PA for hypodermic syringe-friendly packaging. Approval and contract have all been consummated in the absence of official human testing.
Jan. 2008 covert ‘human trials’ of Sanofi-Pasteur H5N1 vaccine is conducted on 350 homeless vagrants in Poland. According to London Telegraph:
and Examiner articles, this results in 21 “instant” deaths and over 200 severely incapacitated or hospitalized.” Development and sales of H5N1 vaccine continues.
February 14, 2008 U.S. Air Force Gen. Gene Renuart, commander of North American Aerospace Defense Command and U.S. Northern Command, and Canadian Air Force Lt.-Gen. Marc Dumais, commander of Canada Command, sign a Civil Assistance Plan that allows the military from one nation to support the armed forces of the other nation during a civil emergency. “Our commands were created by our respective governments to respond to the defense and security challenges of the twenty-first century, and we both realize that these and other challenges are best met through cooperation between friends…. The plan facilitates the military-to-military support of civil authorities once government authorities have agreed on an appropriate response.” Avian Flu response is a part of NorthCom’s mission, and according to Gen. Stubblebine’s analysis, appears to be the primary element in its mission:
March 2008 Haruna Kaita, a pharmaceutical scientists and head of a Nigerian University analyzed the latest WHO vaccine in Indian labs. Sterility agents were among the contaminants found in the samples. According to the local population of the Akha, a Thai hill tribe, pregnant women are forced to receive the vaccine in order to get ID cards for their children. Violent still births and miscarriages result.
June 17, 2008 Dr. David Nabarro, UN Influenza Coordinator, welcomes a donation of 60 million doses of H5N1 Avian Flu vaccine by Sanofi-Pasteur. This adds to the stockpile of a previous donation of 30 million doses by GlaxoSmithKline Dr. Nabarro said that good progress had been made but Avian Flu could still kill as many of 150 million people. Avian Flu still entrenched in Viet Nam, Bangladesh, India, Egypt and India [sic] says Dr. Nabarro. Outbreaks recorded in 60 more countries according to US Influenza Coordinator. But the people who make vaccines are ethical and look out for our best interests don’t they? The cold, hard fact is that vaccine makers are neither ethical nor concerned with health and longevity of their recipients.
1994 – 1999 – A study conducted by Dr. Laure Hewitson at the University of Pittsburgh showed a connection betweein MMR vaccines given to children and several thimerosal mercury containing vaccines injected into children causing Autisic symptomologies.
Monkeys Get Autism-like Reactions to MMR & Other Vaccines In University of Pittsburgh Vaccine Study
Apr 29th, 2012 by Catherine J. Frompovich