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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.Chronological history of vaccination
The apparent danger
of using animal serums foreign to human beings and animal serums foreign to
other animals is reported in medical literature in 1667,
when lambs blood was unsuccessfully used as a human blood transfusion.
1673 Inoculation against smallpox appears in
Denmark.
1712 First record of vaccinations for
smallpox in France.
1717 Innoculation against
smallpox instituted in England by Lady Mary Montague after she returns from
Turkey, where it was in a popular experimental stage at the time
1721 In the United States, a clergyman 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.
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".
1723
First 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. The practice 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.
1790
Edward Jenner buys a medical degree
from St.Andrews University for £15.
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 TB 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 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.
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.
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.
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.
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.
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.
1889
In England, a
royal commission is appointed to inquire into certain aspects of the
vaccination question. The committee would be in session for 7 years and would
issue 6 reports, with the final report in 1896. The result of the final report
was the Vaccination Act of 1898.
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 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.
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 unvaccinated 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 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.
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 BCG 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.
1936
Pertussis vaccine introduced in
the United States. Autism begins to appear in children shortly thereafter.
Diptheria vaccine injures 75 in France.
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
1The idea of "booster shots" arose 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".
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.
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)." In
other words, 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
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
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.
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."
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. 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. Idaho health director Peterson states
that polio only struck vaccinated children in areas where there had been no
cases of polio since the preceeding autumn. In 90% of the cases, the paralysis
occurred in the arm in which the vaccine had been injected. 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.
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.
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.
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 DPT shot.
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.
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.
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 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
World 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 toxoid (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.
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."
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."
1987
Centers for Disease Control
(CDC) releases a study indicating that the Hib (Haemophilus influenzae type B)
vaccine shows an efficacy (effectiveness) rate of 41%. Children were found to
be five times more likely to contract the disease than those not vaccinated.
CDC refuses to give out figures relative to hepatitis vaccinations and HIV+.
Sixty-six Japanese victims of Pertussis vaccine receive huge damage awards from
the Japanese government.
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
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."
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
DPT 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.
squaleneSqualene as 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 molecule 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
"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.
"The
industrialization of the chicken and pork industries is thought to have wrought
these unprecedented changes in avian and swine influenza. No one even got sick
from bird flu for eight decades before a new strain, H5N1, started killing
children in 1997. Likewise, in pigs here in the U.S. swine flu was totally
stable for 8 decades before a pig-bird-human hybrid mutant virus appeared in
commercial pig populations in 1998. It was that strain that combined with a
Eurasian swine flu virus ten years later to spawn the flu pandemic of 2009,
sickening millions of young people around the world. The first hybrid mutant
swine flu virus discovered in the United States was at a factory farm in North
Carolina in which thousands of pregnant sows were confined in "gestation
crates," veal crate-like metal stalls barely larger than their bodies. These
kind of stressful, filthy, overcrowded conditions can provide a breeding ground
for the emergence and spread of new diseases. Studies have shown that measures
as simple as providing straw for pigs so they don't have the immune-crippling
stress of living on bare concrete their whole lives can significantly cut down
on swine flu transmission rates. The American Public Health Association, the
largest organization of public health professionals in the world, has called
for a moratorium on factory farms." - Michael Greger
"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
World Health Organization stated that one of its' primary goals for
the use of a sterility vaccine disguised as a smallpox vaccine was to
"eliminate 150 million excess Sub Saharan Africans". The World Health
Organization also sterilizes over 3 million Philippina women with vaccines and,
through the use of a 5-shot vaccine program for tetanus in South and Central
America, sterilizes millions of women.
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.
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
PLEASE NOTE
THE FOLLOWING ON THE MANUFACTURE OF VACCINES:
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 DNA-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 or retroviruses.
SIVagm is a lentivirus
also a retrovirus. Hepatitis B virus is an hepadnaviru is a DNA 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).
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