Magnesium May Prevent Gallstones

Posted by luputtenan2 on Friday, February 29, 2008

4 Salts

A diet rich in magnesium appears to reduce the
risk developing painful gallstones, according to
findings from a US study.

Consumption of magnesium has been declining over
the years, due in part to the overprocessing of
foods, Dr. Chung-Jyi Tsai and associates note in
their report in the American Journal of
Gastroenterology.

Magnesium deficiency is known to raise triglyceride
levels and decrease HDL ("good") cholesterol levels
in the blood, both of which may increase the risk
of developing gallstones. Still, the long-term
effect of magnesium on the risk of gallstones in
humans was not known until now.

To investigate, Tsai, from the University of
Kentucky Medical Center in Lexington, and
colleagues analyzed data from 42,705 men,
between 40 and 75 years of age, who were enrolled
in the Health Professionals Follow-up Study.
The men were followed from 1986 to 2002.

The subjects were surveyed every 2 years to
assess the occurrence of new illnesses,
including gallbladder disease. Magnesium
consumption was determined with a semiquantitative
food frequency questionnaire sent to the participants
every 4 years.

During follow-up, 2195 men were diagnosed with
gallstone disease, the researchers found.

Compared with the lowest level of total magnesium
intake, the highest intake reduced the risk of
gallstone disease by 33 percent. The same risk
reduction was seen when considering just dietary
magnesium, when supplements were excluded.

"From many studies by this group and others,
it appears that a generally healthy dietary
pattern, with more plant-based foods, fiber,
and increasing complex carbohydrates, and
now increasing magnesium intake will decrease
the risk of symptomatic gallstones," Dr. Cynthia
W. Ko, from the University of Washington in
Seattle, writes in an accompanying editorial.
"This 'healthy' dietary pattern will also help
in prevention of other chronic diseases in
addition to gallstones."

According to Dr. Robert O. Young, a research
scientist at the pH Miracle Living Center, states,
"magnesium is one of four major acid buffers of
dietary and metabolic acids. When we increase
magnesium in the form of carbonate we decrease
the acids that can form gallstones."

http://www.phmiracleliving.com/pHourSalts.htm

Resources:
American Journal of Gastroenterology, February 2008
The pH Miracle
The pH Miracle for Weight Loss
More aboutMagnesium May Prevent Gallstones

Broccoli Sprouts May Protect Against a Cancerous Bladder

Posted by luputtenan2 on Thursday, February 28, 2008


A concentration of broccoli sprouts reduced the
development of bladder tumors in an animal model
by more than half, according to a report in the
March 1 issue of Cancer Research, a journal of
the American Association for Cancer Research.

This finding reinforces human epidemiologic studies
that have suggested that eating cruciferous vegetables
like broccoli is associated with reduced risk for
bladder cancer, according to the studies senior
investigator, Yuesheng Zhang, MD, PhD, professor
of oncology at Roswell Park Cancer Institute.
“Although this is an animal study, it provides
potent evidence that eating vegetables is beneficial
in bladder cancer prevention,” he said.

There is strong evidence that the protective action
of cruciferous vegetables derives at least in part
from isothyiocyanates (ITCs), a group of phytochemicals
with well-known cancer preventive activities.

“The bladder is particularly responsive to this group
of natural chemicals,” Zhang said. “In our experiments,
the broccoli sprout ITCs after oral administration
were selectively delivered to the bladder tissues
through urinary excretion.”

Other cruciferous vegetables with ITCs include mature
broccoli, cabbage, kale, collard greens and others all
contained in Dr. Young's newest whole food product called
pHruits and pHolage.

http://www.phmiracleliving.com/phruits.htm

Broccoli sprouts have approximately 30 times more ITCs
than mature broccoli, and the sprout extract used by
the researchers contains approximately 600 times as
much.

Although animals that had the most protection against
development of bladder cancer were given high doses
of the extract, Zhang said humans at increased risk
for this cancer likely do not need to eat huge amounts
of broccoli sprouts in order to derive protective
benefits.

“Epidemiologic studies have shown that dietary ITCs
and cruciferous vegetable intake are inversely
associated with bladder cancer risk in humans. It
is possible that ITC doses much lower than those
given to the rats in this study may be adequate
for bladder cancer prevention,” he said.

Zhang and his colleagues tested the ability of
the concentrate to prevent bladder tumors in
five groups of rats. The first group acted as a
control, while the second group was given only
the broccoli extract to test for safety. The
remaining three groups were given a chemical, N-butyl-N-(4-hydroxybutyl) nitrosamine (BBN)
in drinking water, which induces bladder cancer.
Two of these groups were given the broccoli
extract in diet, beginning two weeks before
the carcinogenic chemical was delivered.

In the control group and the group given only
the extract, no tumors developed, and there was
no toxicity from the extract in the rats.

About 96 percent of animals given only BBN
developed an average of almost two tumors each
of varying sizes. By comparison, about 74 percent
of animals given a low dose of the extract
developed cancer, and the number of tumors per
rat was 1.39. The group given the high dose of
extract had even fewer tumors. About 38 percent
of this high-dose group developed cancer, and the
average number of tumors per animal was only .46
and, unlike the other animals, the majority were
very small in size.

To learn more about the anti-oxidant and ITC benefits
of Dr. Young's newest whole food organic pHruits
and pHolage, with concentrated organic broccoli sprouts
go to:

http://www.phmiracleliving.com/phruits.htm
More aboutBroccoli Sprouts May Protect Against a Cancerous Bladder

Government Concedes - Vaccines Cause Autism!

Posted by luputtenan2


I have been fighting for this truth to be
revealed for years. I have worked with the
autism spectrum for years by balancing
biochemistries and clearing the
bowel congestion I find in all cases of
autism.

Finally my work is vindicated!

http://www.huffingtonpost.com/david-kirby/
government-concedes-vacci_b_88323.html

Government Concedes Vaccine - Autism Case in
Federal Court - Now What?

By David Kirby
February 25, 2008

After years of insisting there is no evidence
to link vaccines with the onset of autism
spectrum disorder (ASD), the US government
has quietly conceded a vaccine-autism case
in the Court of Federal Claims.

The unprecedented concession was filed on
November 9, and sealed to protect the
plaintiff's identify. It was obtained
through individuals unrelated to the case.

The claim, one of 4,900 autism cases currently
pending in Federal "Vaccine Court," was conceded
by US Assistant Attorney General Peter Keisler
and other Justice Department officials, on behalf
of the Department of Health and Human Services,
the "defendant" in all Vaccine Court cases.

The child's claim against the government --
that mercury-containing vaccines were the cause
of her autism -- was supposed to be one of
three "test cases" for the thimerosal-autism
theory currently under consideration by a
three-member panel of Special Masters, the
presiding justices in Federal Claims Court.

Keisler wrote that medical personnel at the
HHS Division of Vaccine Injury Compensation
(DVIC) had reviewed the case and "concluded
that compensation is appropriate."

The doctors conceded that the child was
healthy and developing normally until her
18-month well-baby visit, when she received
vaccinations against nine different diseases
all at once (two contained thimerosal).

Days later, the girl began spiraling downward
into a cascade of illnesses and setbacks that,
within months, presented as symptoms of autism,
including: No response to verbal direction;
loss of language skills; no eye contact; loss
of "relatedness;" insomnia; incessant screaming;
arching; and "watching the florescent lights
repeatedly during examination."

Seven months after vaccination, the patient
was diagnosed by Dr. Andrew Zimmerman, a
leading neurologist at the Kennedy Krieger
Children's Hospital Neurology Clinic, with
"regressive encephalopathy (brain disease)
with features consistent with autistic
spectrum disorder, following normal development."
The girl also met the Diagnostic and Statistical
Manual for Mental Disorders (DSM-IV) official
criteria for autism.

In its written concession, the government said
the child had a pre-existing mitochondrial
disorder that was "aggravated" by her shots,
and which ultimately resulted in an ASD diagnosis.

"The vaccinations received on July 19, 2000,
significantly aggravated an underlying
mitochondrial disorder," the concession says,
"which predisposed her to deficits in cellular
energy metabolism, and manifested as a regressive
encephalopathy with features of ASD."

To read the rest of Mr. Kirby's piece and
to post your comments, please visit

http://www.huffingtonpost.com/david-kirby/
government-concedes-vacci_b_88323.html
More aboutGovernment Concedes - Vaccines Cause Autism!

Low Cholesterol May Raise The Risk For Stomach Cancer

Posted by luputtenan2 on Wednesday, February 27, 2008


Low Cholesterol May Raise The Risk of a Cancerous
Stomach.

Why?

Because cholesterol is a major buffer of dietary
and metabolic acids that can cause the breakdown
of cells and tissues leading to a cancerous state.

It is the stomach that produces the body's number
one acid buffer - sodium bicarbonate.

When the body needs more sodium bicarbonate to buffer
dietary and metabolic acid there is an equal amount
of hydrochloric acid that is secreted into the stomach.
The newly created sodium bicarbonate by the stomach
is either used to buffer the acids of food in the stomach
or taken up into the blood stream to buffer metabolic acids
when cholesterol is not present.

Bottom line, it is the body's increased need for
cholesterol to buffer acids in the extracellular
fluids. When cholesterol is not present to buffer
dietary or metabolic acids then the stomach kicks
in and starts producing sodium bicarbonate.
This process leaves toxic hydrochloric
acid in the gastric pits of the stomach that can
destroy stomach cells leading to ulcerations and a
cancerous stomach.

Japanese researchers are suggesting that people with
very low cholesterol levels seem to be at
increased risk of developing stomach cancer. This
is because of the body's increased need for sodium
bicarbonate and the residues of hydrochloric acid
that is left to ferment the stomach leading to
a cancerous stomach.

Some studies have linked low cholesterol levels to
higher death rates from cancer in general, Dr. Kouichi
Asano, of Kyushu University, Fukuoka, and colleagues
explain in the International Journal of Cancer.
"With respect to gastric cancer, a limited number
of studies suggest this inverse association, while
others do not."

The researcher looked into this in a study involving
some 2,600 residents of Hisayama, Japan, who were
followed for 14 years.

Gastric cancers developed in 97 subjects. After
accounting for age and gender, stomach cancer rates
rose significantly with descending cholesterol level.
For example, among subjects with the highest cholesterol
levels, the gastric cancer rate was the equivalent
of 2.1 cases per 1000 persons per year; among those
with the lowest cholesterol, the rate was 3.9 per
1000 person-years.

"Our data suggest that patients with low serum
cholesterol should consider regular gastro-intestinal
examination for the prevention of gastric cancer,"
the investigators conclude.

To prevent a cancerous condition, including stomach
cancer one needs to include liberal amounts of
sodium chloride (salt) and medium and long chain
fats.

According to Dr. Robert O. Young, a research
scientist from the pH Miracle Living Center, states,
"the stomach is an organ of contribution not an
organ of digestion. Its main contribution to the
health and well-being of the body is to produce
alkaline salts of sodium and potassium bicarbonate.
The purpose of the stomach in producing these
alkaline salts is to buffer the acids of diet and
metabolism for maintaining the alkaline design of
the body fluids and thus protecting the alkaline
integrity of the cells."

"To prevent and/or reverse a cancerous condition one
must incorporate liberal amounts of sodium and
potassium bicarbonate and good healthy fats."

To learn more about the importance of mineral
salts and good oils in the diet in the preventing
a cancerous condition, even a cancerous stomach, go to:

http://www.phmiracleliving.com/pHourSalts.htm
http://www.phmiracleliving.com/phlavor.htm
http://www.phmiracleliving.com/cla.htm
http://www.phmiracleliving.com/avocado-oil.htm

Resources:
International Journal of Cancer, February 15, 2008.
The pH Miracle for Cancer
More aboutLow Cholesterol May Raise The Risk For Stomach Cancer

Vaccination = A Moral Crisis

Posted by luputtenan2


The following is a link concerning acidic vaccines
and their link to autism and other neurological dis-ease.
This link and article was uncovered by using the Freedom
of Information Act request, by John F. Kennedy Jr.
My hope is when you read this article it will be
enough to really motivate you to rally against the
powers that be who blatantly hide the truth about
the toxic acidic effects of ALL vaccines that jeopardize
the health and well-being of every child across our
country and the world! Please write your
congressman or congresswoman today and ask to put an
end to ALL mandatory toxic acidic vaccines.

According to Dr. Robert O. Young, "vaccinations are all
acidic and toxic to the body and provide no true immunity.
True immunity is found in a person who is maintaining the
alkaline design of their body fluids at 7.365 or better
with an alkaline lifestyle and diet!"

http://groups.google.com/group/misc.kids.pregnancy/msg/
4847350dae3bb353?

Uncovered via the FREEDOM OF INFORMATION ACT reported
by ROBERT F KENNEDY JR

Deadly Immunity

Robert F. Kennedy Jr. investigates the government
cover-up of a mercury/autism scandal

By ROBERT F. KENNEDY JR.

In June 2000, a group of top government scientists
and health officials gathered for a meeting at the
isolated Simpsonwood conference center in Norcross,
Georgia. Convened by the Centers for Disease Control
and Prevention, the meeting was held at this Methodist
retreat center, nestled in wooded farmland next to
the Chattahoochee River, to ensure complete secrecy.
The agency had issued no public announcement of the
session -- only private invitations to fifty-two
attendees. There were high-level officials from the
CDC and the Food and Drug Administration, the top
vaccine specialist from the World Health Organization
in Geneva and representatives of every major vaccine
manufacturer, including GlaxoSmithKline, Merck, Wyeth
and Aventis Pasteur. All of the scientific data under
discussion, CDC officials repeatedly reminded the
participants, was strictly "embargoed." There would
be no making photocopies of documents, no taking
papers with them when they left.

The federal officials and industry representatives
had assembled to discuss a disturbing new study that
raised alarming questions about the safety of a host
of common childhood vaccines administered to infants
and young children. According to a CDC epidemiologist
named Tom Verstraeten, who had analyzed the agency's
massive database containing the medical records of
100,000 children, a mercury-based preservative in the
vaccines -- thimerosal -- appeared to be responsible
for a dramatic increase in autism and a host of other
neurological disorders among children. "I was actually
stunned by what I saw," Verstraeten told those assembled
at Simpsonwood, citing the staggering number of earlier
studies that indicate a link between thimerosal and
speech delays, attention-deficit disorder, hyperactivity
and autism. Since 1991, when the CDC and the FDA
had recommended that three additional vaccines laced
with the preservative be given to extremely young
infants -- in one case, within hours of birth --
the estimated number of cases of autism had
increased fifteenfold, from one in every 2,500
children to one in 166 children.

Even for scientists and doctors accustomed to confronting
issues of life and death, the findings were frightening.
"You can play with this all you want," Dr. Bill Weil,
a consultant for the American Academy of Pediatrics,
told the group. The results "are statistically
significant." Dr. Richard Johnston, an immunologist
and pediatrician from the University of Colorado whose
grandson had been born early on the morning of the
meeting'sfirst day, was even more alarmed. "My gut
feeling?" he said. "Forgive this personal comment --
I do not want my grandson to get a thimerosal-containing
vaccine until we know better what is going on."

But instead of taking immediate steps to alert the public
and rid the vaccine supply of thimerosal, the officials
and executives at Simpsonwood spent most of the next
two days discussing how to cover up the damaging data.
According to transcripts obtained under the Freedom of
Information Act, many at the meeting were concerned
about how the damaging revelations about thimerosal
would affect the vaccine industry's bottom line. "We
are in a bad position from the standpoint of defending
any lawsuits," said Dr. Robert Brent, a pediatrician
at the Alfred I. duPont Hospital for Children in Delaware.
"This will be a resource to our very busy plaintiff
attorneys in this country." Dr. Bob Chen, head of
vaccine safety for the CDC, expressed relief that
"given the sensitivity of the information, we have
been able to keep it out of the hands of, let's say,
less responsible hands." Dr. John Clements, vaccines
adviser at the World Health Organization, declared
flatly that the study "should not have been done at
all" and warned that the results "will be taken by
others and will be used in ways beyond the control of
this group. The research results have to be handled."

In fact, the government has proved to be far more
adept at handling the damage than at protecting
children's health. The CDC paid the Institute of
Medicine to conduct a new study to whitewash the
risks of thimerosal, ordering researchers to "rule
out" the chemical's link to autism. It withheld
Verstraeten's findings, even though they had been
slated for immediate publication, and told other
scientists that his original data had been "lost"
and could not be replicated. And to thwart the
Freedom of Information Act, it handed its giant
database of vaccine records over to a private company,
declaring it off-limits to researchers. By the time
Verstraeten finally published his study in 2003,
he had gone to work for GlaxoSmithKline and reworked
his data to bury the link between thimerosal and
autism.

Vaccine manufacturers had already begun to phase
thimerosal out of injections given to American
infants -- but they continued to sell off their
mercury-based supplies of vaccines until last year.
The CDC and FDA gave them a hand, buying up the tainted
vaccines for export to developing countries and
allowing drug companies to continue using the
preservative in some American vaccines -- including
several pediatric flu shots as well as tetanus boosters
routinely given to eleven-year-olds.

The drug companies are also getting help from powerful
lawmakers in Washington. Senate Majority Leader Bill
Frist, who has received $873,000 in contributions from
the pharmaceutical industry, has been working to
immunize vaccine makers from liability in 4,200
lawsuits that have been filed by the parents of injured
children. On five separate occasions, Frist has tried
to seal all of the government's vaccine-related
documents -- including the Simpsonwood transcripts --
and shield Eli Lilly, the developer of thimerosal,
from subpoenas. In 2002, the day after Frist quietly
slipped a rider known as the "Eli Lilly Protection
Act" into a homeland security bill, the company
contributed $10,000 to his campaign and bought 5,000
copies of his book on bioterrorism. The measure was
repealed by Congress in 2003 -- but earlier this year,
Frist slipped another provision into an anti-terrorism
bill that would deny compensation to children suffering
from vaccine-related brain disorders. "The lawsuits
are of such magnitude that they could put vaccine
producers out of business and limit our capacity to
deal with a biological attack by terrorists," says
Andy Olsen, a legislative assistant to Frist.

Even many conservatives are shocked by the government's
effort to cover up the dangers of thimerosal. Rep.
Dan Burton, a Republican from Indiana, oversaw a
three-year investigation of thimerosal after his
grandson was diagnosed with autism. "Thimerosal
used as a preservative in vaccines is directly
related to the autism epidemic," his House Government
Reform Committee concluded in its final report.
"This epidemic in all probability may have been
prevented or curtailed had the FDA not been asleep
at the switch regarding a lack of safety data
regarding injected thimerosal, a known neurotoxin."
The FDA and other public-health agencies failed to
act, the committee added, out of "institutional
malfeasance for self protection" and "misplaced
protectionism of the pharmaceutical industry."

The story of how government health agencies colluded
with Big Pharma to hide the risks of thimerosal from
the public is a chilling case study of institutional
arrogance, power and greed. I was drawn into the
controversy only reluctantly. As an attorney and
environmentalist who has spent years working on
issues of mercury toxicity, I frequently met mothers
of autistic children who were absolutely convinced
that their kids had been injured by vaccines.
Privately, I was skeptical.

I doubted that autism could be blamed on a single source,
and I certainly understood the government's need to
reassure parents that vaccinations are safe; the
eradication of deadly childhood diseases depends on
it. I tended to agree with skeptics like Rep. Henry
Waxman, a Democrat from California, who criticized
his colleagues on the House Government Reform Committee
for leaping to conclusions about autism and vaccinations.
"Why should we scare people about immunization," Waxman
pointed out at one hearing, "until we know the facts?"

It was only after reading the Simpsonwood transcripts,
studying the leading scientific research and talking
with many of the nation's pre-eminent authorities on
mercury that I became convinced that the link between
thimerosal and the epidemic of childhood neurological
disorders is real. Five of my own children are members
of the Thimerosal Generation -- those born between
1989 and 2003 -- who received heavy doses of mercury
from vaccines. "The elementary grades are overwhelmed
with children who have symptoms of neurological or
immune-system damage," Patti White, a school nurse,
told the House Government Reform Committee in 1999.
"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."

More than 500,000 kids currently suffer from autism,
and pediatricians diagnose more than 40,000 new cases
every year. The disease was unknown until 1943, when
it was identified and diagnosed among eleven children
born in the months after thimerosal was first added
to baby vaccines in 1931.

Some skeptics dispute that the rise in autism is
caused by thimerosal-tainted vaccinations. They
argue that the increase is a result of better
diagnosis -- a theory that seems questionable
at best, given that most of the new cases of autism
are clustered within a single generation of children.
"If the epidemic is truly an artifact of poor
diagnosis," scoffs Dr. Boyd Haley, one of the
world's authorities on mercury toxicity, "then where
are all the twenty-year-old autistics?" Other
researchers point out that Americans are exposed
to a greater cumulative "load" of mercury than
ever before, from contaminated fish to dental
fillings, and suggest that thimerosal in vaccines
may be only part of a much larger problem.
It's a concern that certainly deserves far more
attention than it has received -- but it overlooks
the fact that the mercury concentrations in
vaccines dwarf other sources of exposure to our
children.

What is most striking is the lengths to which many
of the leading detectives have gone to ignore --
and cover up -- the evidence against thimerosal.
From the very beginning, the scientific case against
the mercury additive has been overwhelming. The
preservative, which is used to stem fungi and
bacterial growth in vaccines, contains ethylmercury,
a potent neurotoxin. Truckloads of studies have
shown that mercury tends to accumulate in the brains
of primates and other animals after they are injected
with vaccines -- and that the developing brains of
infants are particularly susceptible. In 1977,
a Russian study found that adults exposed to much
lower concentrations of ethylmercury than those given
to American children still suffered brain damage years
later. Russia banned thimerosal from children's
vaccines twenty years ago, and Denmark, Austria,
Japan, Great Britain and all the Scandinavian countries
have since followed suit.

"You couldn't even construct a study that shows
thimerosal is safe," says Haley, who heads the
chemistry department at the University of Kentucky.
"It's just too darn toxic. If you inject thimerosal
into an animal, its brain will sicken. If you apply
it to living tissue, the cells die. If you put it
in a petri dish, the culture dies. Knowing these
things, it would be shocking if one could inject
it into an infant without causing damage."

Internal documents reveal that Eli Lilly, which
first developed thimerosal, knew from the start
that its product could cause damage -- and even
death -- in both animals and humans. In 1930, the
company tested thimerosal by administering it to
twenty-two patients with terminal meningitis, all
of whom died within weeks of being injected --
a fact Lilly didn't bother to report in its study
declaring thimerosal safe. In 1935, researchers
at another vaccine manufacturer, Pittman-Moore,
warned Lilly that its claims about thimerosal's
safety "did not check with ours." Half the dogs
Pittman injected with thimerosal-based vaccines
became sick, leading researchers there to declare
the preservative "unsatisfactory as a serum intended
for use on dogs."

In the decades that followed, the evidence against
thimerosal continued to mount. During the Second
World War, when the Department of Defense used the
preservative in vaccines on soldiers, it required
Lilly to label it "poison." In 1967, a study in
Applied Microbiology found that thimerosal killed
mice when added to injected vaccines.

Four years later, Lilly's own studies discerned that
thimerosal was "toxic to tissue cells" in concentrations
as low as one part per million -- 100 times weaker
than the concentration in a typical vaccine. Even so,
the company continued to promote thimerosal as
"nontoxic" and also incorporated it into topical
disinfectants. In 1977, ten babies at a Toronto
hospital died when an antiseptic preserved with
thimerosal was dabbed onto their umbilical cords.

In 1982, the FDA proposed a ban on over-the-counter
products that contained thimerosal, and in 1991 the
agency considered banning it from animal vaccines.
But tragically, that same year, the CDC recommended
that infants be injected with a series of mercury-
laced vaccines. Newborns would be vaccinated for
hepatitis B within twenty-four hours of birth, and
two-month-old infants would be immunized for
haemophilus influenzae B and diphtheria-tetanus-
pertussis.

The drug industry knew the additional vaccines
posed a danger. The same year that the CDC approved
the new vaccines, Dr. Maurice Hilleman, one of the
fathers of Merck's vaccine programs, warned
the company that six-month-olds who were administered
the shots would suffer dangerous exposure to mercury.
He recommended that thimerosal be discontinued,
"especially when used on infants and children,"
noting that the industry knew of nontoxic
alternatives. "The best way to go," he added,
"is to switch to dispensing the actual vaccines
without adding preservatives."

For Merck and other drug companies, however, the
obstacle was money. Thimerosal enables the
pharmaceutical industry to package vaccines in
vials that contain multiple doses, which require
additional protection because they are more easily
contaminated by multiple needle entries.

The larger vials cost half as much to produce as
smaller, single-dose vials, making it cheaper for
international agencies to distribute them to
impoverished regions at risk of epidemics. Faced
with this "cost consideration," Merck ignored
Hilleman's warnings, and government officials
continued to push more and more thimerosal-based
vaccines for children. Before 1989, American
preschoolers received only three vaccinations --
for polio, diphtheria-tetanus-pertussis and
measles-mumps-rubella. A decade later, thanks
to federal recommendations, children were receiving
a total of twenty-two immunizations by the time
they reached first grade.

As the number of vaccines increased, the rate of
autism among children exploded. During the 1990s,
40 million children were injected with thimerosal-
based vaccines, receiving unprecedented levels of
mercury during a period critical for brain development.
Despite the well-documented dangers of thimerosal,
it appears that no one bothered to add up the cumulative
dose of mercury that children would receive from
the mandated vaccines. "What took the FDA so long
to do the calculations?" Peter Patriarca, director
of viral products for the agency, asked in an e-mail
to the CDC in 1999. "Why didn't CDC and the advisory
bodies do these calculations when they rapidly
expanded the childhood immunization schedule?"

But by that time, the damage was done. Infants who
received all their vaccines, plus boosters, by the
age of six months were being injected with levels of
ethylmercury 187 times greater than the EPA's limit
for daily exposure to methylmercury, a related
neurotoxin. Although the vaccine industry insists
that ethylmercury poses little danger because it
breaks down rapidly and is removed by the body, several
studies -- including one published in April by the
National Institutes of Health -- suggest that
ethylmercury is actually more toxic to developing
brains and stays in the brain longer than
methylmercury.

Officials responsible for childhood immunizations insist
that the additional vaccines were necessary to protect
infants from disease and that thimerosal is still
essential in developing nations, which, they often
claim, cannot afford the single-dose vials that
don't require a preservative. Dr. Paul Offit, one
of CDC's top vaccine advisers, told me, "I think if
we really have an influenza pandemic -- and certainly we
will in the next twenty years, because we always do --
there's no way on God's earth that we immunize 280
million people with single-dose vials. There has to
be multidose vials."

But while public-health officials may have been well-
intentioned, many of those on the CDC advisory committee
who backed the additional vaccines had close ties to
the industry. Dr. Sam Katz, the committee's chair, was
a paid consultant for most of the major vaccine makers
and shares a patent on a measles vaccine with Merck,
which also manufactures the hepatitis B vaccine. Dr.
Neal Halsey, another committee member, worked as a
researcher for the vaccine companies and received
honoraria from Abbott Labs for his research on the
hepatitis B vaccine.

Indeed, in the tight circle of scientists who work on
vaccines, such conflicts of interest are common. Rep.
Burton says that the CDC "routinely allows scientists
with blatant conflicts of interest to serve on
intellectual advisory committees that make
recommendations on new vaccines," even though they
have "interests in the products and companies for
which they are supposed to be providing unbiased
oversight." The House Government Reform Committee
discovered that four of the eight CDC advisers who
approved guidelines for a rotavirus vaccine laced
with thimerosal "had financial ties to the
pharmaceutical companies that were developing
different versions of the vaccine."

Offit, who shares a patent on the vaccine,
acknowledged to me that he "would make money" if
his vote to approve it eventually leads to a
marketable product. But he dismissed my suggestion
that a scientist's direct financial stake in CDC
approval might bias his judgment. "It provides no
conflict for me," he insists. "I have simply been
informed by the process, not corrupted by it. When
I sat around that table, my sole intent was trying
to make recommendations that best benefited the
children in this country. It's offensive to say that
physicians and public-health people are in the pocket
of industry and thus are making decisions that they
know are unsafe for children. It's just not the way
it works."

Other vaccine scientists and regulators gave me
similar assurances. Like Offit, they view themselves
as enlightened guardians of children's health, proud
of their "partnerships" with pharmaceutical companies,
immune to the seductions of personal profit, besieged
by irrational activists whose anti-vaccine campaigns
are endangering children's health. They are often
resentful of questioning. "Science," says Offit,
"is best left to scientists."

Still, some government officials were alarmed by
the apparent conflicts of interest. In his e-mail to
CDC administrators in 1999, Paul Patriarca of the FDA
blasted federal regulators for failing to adequately
scrutinize the danger posed by the added baby
vaccines. "I'm not sure there will be an easy way out
of the potential perception that the FDA, CDC and
immunization-policy bodies may have been asleep at
the switch re: thimerosal until now," Patriarca wrote.
The close ties between regulatory officials and the
pharmaceutical industry, he added, "will also raise
questions about various advisory bodies regarding
aggressive recommendations for use" of thimerosal
in child vaccines.

If federal regulators and government scientists
failed to grasp the potential risks of thimerosal
over the years, no one could claim ignorance after
the secret meeting at Simpsonwood. But rather than
conduct more studies to test the link to autism and
other forms of brain damage, the CDC placed politics
over science. The agency turned its database on
childhood vaccines -- which had been developed largely
at taxpayer expense -- over to a private agency,
America's Health Insurance Plans, ensuring that it
could not be used for additional research. It also
instructed the Institute of Medicine, an advisory
organization that is part of the National Academy of
Sciences, to produce a study debunking the link
between thimerosal and brain disorders. The CDC
"wants us to declare, well, that these things are
pretty safe," Dr. Marie McCormick, who chaired the
IOM's Immunization Safety Review Committee, told her
fellow researchers when they first met in January 2001.
"We are not ever going to come down that [autism] is
a true side effect" of thimerosal exposure. According
to transcripts of the meeting, the committee's chief
staffer, Kathleen Stratton, predicted that the IOM
would conclude that the evidence was "inadequate to
accept or reject a causal relation" between thimerosal
and autism. That, she added, was the result "Walt
wants" -- a reference to Dr. Walter Orenstein, director
of the National Immunization Program for the CDC.

For those who had devoted their lives to promoting
vaccination, the revelations about thimerosal
threatened to undermine everything they had worked
for. "We've got a dragon by the tail here," said Dr.
Michael Kaback, another committee member. "The more
negative that [our] presentation is, the less likely
people are to use vaccination, immunization -- and we
know what the results of that will be. We are kind
of caught in a trap. How we work our way out of the
trap, I think is the charge."

Even in public, federal officials made it clear that
their primary goal in studying thimerosal was to
dispel doubts about vaccines. "Four current studies
are taking place to rule out the proposed link
between autism and thimerosal," Dr. Gordon Douglas,
then-director of strategic planning for vaccine research
at the National Institutes of Health, assured a
Princeton University gathering in May 2001. "In order
to undo the harmful effects of research claiming to
link the [measles] vaccine to an elevated risk of autism,
we need to conduct and publicize additional studies to
assure parents of safety." Douglas formerly served as
president of vaccinations for Merck, where he ignored
warnings about thimerosal's risks.

In May of last year, the Institute of Medicine issued
its final report. Its conclusion: There is no proven
link between autism and thimerosal in vaccines. Rather
than reviewing the large body of literature describing
the toxicity of thimerosal, the report relied on four
disastrously flawed epidemiological studies examining
European countries, where children received much smaller
doses of thimerosal than American kids. It also cited a
new version of the Verstraeten study, published in the
journal Pediatrics, that had been reworked to reduce
the link between thimerosal and autism. The new study
included children too young to have been diagnosed
with autism and overlooked others who showed signs
of the disease. The IOM declared the case closed and --
in a startling position for a scientific body --
recommended that no further research be conducted.

The report may have satisfied the CDC, but it convinced no
one! Rep. David Weldon, a Republican physician from
Florida who serves on the House Government Reform
Committee, attacked the Institute of Medicine, saying
it relied on a handful of studies that were "fatally
flawed" by "poor design" and failed to represent "all
the available scientific and medical research." CDC
officials are not interested in an honest search for
the truth, Weldon told me, because "an association
between vaccines and autism would force them to admit
that their policies irreparably damaged thousands of
children. Who would want to make that conclusion
about themselves?"

Under pressure from congress, parents and a few of its
own panel members, the Institute of Medicine reluctantly
convened a second panel to review the findings of the
first. In February, the new panel, composed of
different scientists, criticized the earlier panel
for its lack of transparency and urged the CDC to
make its vaccine database available to the public.

So far, though, only two scientists have managed to
gain access. Dr. Mark Geier, president of the
Genetics Center of America, and his son, David,
spent a year battling to obtain the medical records
from the CDC. Since August 2002, when members of
Congress pressured the agency to turn over the data, the
Geiers have completed six studies that demonstrate a
powerful correlation between thimerosal and
neurological damage in children. One study, which
compares the cumulative dose of mercury received by
children born between 1981 and 1985 with those born
between 1990 and 1996, found a "very significant
relationship" between autism and vaccines. Another
study of educational performance found that kids who
received higher doses of thimerosal in vaccines were
nearly three times as likely to be diagnosed with
autism and more than three times as likely to suffer
from speech disorders and mental retardation. Another
soon-to-be published study shows that autism rates
are in decline following the recent elimination of
thimerosal from most vaccines.

As the federal government worked to prevent scientists
from studying vaccines, others have stepped in to study
the link to autism. In April, reporter Dan Olmsted of
UPI undertook one of the more interesting studies
himself. Searching for children who had not been
exposed to mercury in vaccines -- the kind of population
that scientists typically use as a "control" in
experiments -- Olmsted scoured the Amish of Lancaster
County, Pennsylvania, who refuse to immunize their
infants. Given the national rate of autism, Olmsted
calculated that there should be 130 autistics among
the Amish. He found only four. One had been exposed
to high levels of mercury from a power plant. The other
three -- including one child adopted from outside
the Amish community -- had received their vaccines.

At the state level, many officials have also conducted
in-depth reviews of thimerosal. While the Institute
of Medicine was busy whitewashing the risks, the Iowa
legislature was carefully combing through all of the
available scientific and biological data. "After three
years of review, I became convinced there was sufficient
credible research to show a link between mercury and
the increased incidences in autism," says state Sen.
Ken Veenstra, a Republican who oversaw the investigation.
"The fact that Iowa's 700 percent increase in autism
began in the 1990s, right after more and more vaccines
were added to the children's vaccine schedules, is solid
evidence alone." Last year, Iowa became the first state
to ban mercury in vaccines, followed by California.
Similar bans are now under consideration in thirty-two
other states.

But instead of following suit, the FDA continues to
allow manufacturers to include thimerosal in scores
of over-the-counter medications as well as steroids
and injected collagen. Even more alarming, the
government continues to ship vaccines preserved
with thimerosal to developing countries -- some of
which are now experiencing a sudden explosion in autism
rates. In China, where the disease was virtually unknown
prior to the introduction of thimerosal by U.S.
drug manufacturers in 1999, news reports indicate that
there are now more than 1.8 million autistics. Although
reliable numbers are hard to come by, autistic disorders
also appear to be soaring in India, Argentina, Nicaragua
and other developing countries that are now using
thimerosal-laced vaccines. The World Health
Organization continues to insist thimerosal is safe, but
it promises to keep the possibility that it is linked
to neurological disorders "under review."

I devoted time to study this issue because I believe
that this is a moral crisis that must be addressed.
If, as the evidence suggests, our public-health
authorities knowingly allowed the pharmaceutical
industry to poison an entire generation of American
children, their actions arguably constitute one of
the biggest scandals in the annals of American
medicine. "The CDC is guilty of incompetence and
gross negligence," says Mark Blaxill, vice president
of Safe Minds, a nonprofit organization concerned
about the role of mercury in medicines. "The damage
caused by vaccine exposure is massive. It's bigger
than asbestos, bigger than tobacco, bigger than
anything you've ever seen."

It's hard to calculate the damage to our country --
and to the international efforts to eradicate epidemic
diseases -- if Third World nations come to believe
that America's most heralded foreign-aid initiative
is poisoning their children. It's not difficult to
predict how this scenario will be interpreted by
America's enemies abroad. The scientists and researchers --
many of them sincere, even idealistic -- who are
participating in efforts to hide the science on
thimerosal claim that they are trying to advance the
lofty goal of protecting children in developing nations
from disease pandemics. They are badly misguided.
Their failure to come clean on thimerosal will
come back horribly to haunt our country and the
world's poorest populations.

To learn more about the toxic acidic ingredients in
all vaccinations may I suggest reading, Sick and Tired,
and the technical essay, "A Second Thought About
Viruses, Vaccines and the HIV Hypothesis."

http://www.phmiracleliving.com/books.htm

As someone that looks to improve their health we are pleased to offer you this free audio, an excerpt of a powerful two hour interview with Dr Robert O. Young and Anthony Robbins. (it is free to listen!)

Click here to listen: http://www.1shoppingcart.com/app/?Clk=1870270

I trust you'll enjoy this...

Not part of our healing alkaline community?
Visit our website at:

www.phmiracleliving.com

To learn more about the science of Dr. Robert and Shelley Young go to:

www.articlesofhealth.blogspot.com

'Miracles happen not in opposition to nature, but in opposition to what we know of nature.' St. Augustine

'Any sufficiently advanced technology is indistinguishable from magic' ....Arthur C. Clarke

'There are only two ways to live your life. One, is as though there are no miracles. The other is as though everything is a miracle.' Albert Einstein

Copyright 2007 Dr. Robert and Shelley Young

pH Miracle Living Center
16390 Dia Del Sol
Valley Center, California 92082 US
More aboutVaccination = A Moral Crisis

Refined Carbohydartes May Be The Cause Of Esophageal Cancer

Posted by luputtenan2


Cases of esophageal cancer (adenocarcinoma) in
the U.S. have risen in recent decades from 300,000
cases in 1973 to 2.1 million in 2001 at age-adjusted
rates. A new study published in The American Journal
of Gastroenterology shows that these rates in the U.S.
closely mirrored trends of increased carbohydrate
intake and obesity from 1973-2001.

The study illustrates what may be a public heath
concern as the composition of U.S. diets changes
and total carbohydrate and refined carbohydrate
intakes increase. Obesity is a risk factor for many
cancerous types, and a diet that includes a high
percentage of acid forming refined carbohydrates is
a common contributor to obesity. Carbohydrates
were also unique in that no other studied nutrients
were found to correlate with esophageal cancer rates.

"The causes of esophageal cancer are the result of
acidic lifestyle and dietary choices which includes
the ingestion of refined and complex carbohydrates,"
states Dr.Robert O. Young, a research scientist at
the pH Miracle Living Center, in San Diego,
California.

Despite recent advances in treatment, esophageal
cancer has a poor prognosis. The five-year rate
of survival for esophageal cancer remains below
20 percent and is the eighth-leading cause of
cancer related death in American men.

“If we can reverse the trends in refined carbohydrate
intake and obesity in the U.S., we may be able to
reduce the incidence of esophageal cancer,” says
Dr. Li Li, senior author of the study.

Dr. Young suggests that, "an alkaline lifestyle and
diet will eliminate obesity in America as well as
cancer, including esophageal cancer."

To learn more about cancer and how to prevent or
reverse a cancerous condition listen to:

The pH Miracle for Cancer
http://www.phmiracleliving.com/audios.htm
More aboutRefined Carbohydartes May Be The Cause Of Esophageal Cancer

Low or No Protein Diet May Extend Life

Posted by luputtenan2


The key to longevity is eating less protein or
better still no animal protein -- and not just fewer
calories and less acidity, as has previously been
thought -- scientists have discovered.

"Animals that eat less live longer -- up to a point,"
says Professor Stephen Simpson of the University of
Sydney's School of Biological Sciences. "Our research
using animal models shows the balance of protein to
carbohydrate in the diet is critical."

The idea that restricting food intake without
malnutrition prolongs life has become a core
belief in gerontology research, Professor Simpson
says. "We know dietary restriction extends life in
yeasts, fruit flies, worms, mice and monkeys, and
it is widely held that the same affect should be
true for humans."

But scientists couldn't be sure whether it was the
restriction of calories in itself, or the restriction
of specific nutrients, that affected aging. But now
Professor Simpson and colleagues at Seoul University,
Auckland University, UNSW and Macquarie have measured
for the first time in any organism the relationship
between diet, nutrient intake, lifespan and
reproduction

Using new techniques developed by Professor Simpson
and Professor David Raubenheimer (Auckland) the team
showed in the fruit fly that calorie restriction is
not responsible for extending lifespan: rather the
balance of protein to carbohydrate in the diet was
critical.

"Flies lived longest when the diet contained a low
percentage of protein, and died sooner the more
protein they consumed," says Professor Simpson.
"But protein is needed for reproduction -- so flies
are faced with a conundrum: eat less protein and
live longer, or eat more protein and lay more eggs?"

Professor Simpson said his team 'asked' the flies
what they preferred. "When offered a choice, flies
behaved like nutrient-seeking missiles, unerringly
mixing a relatively high protein diet that
maximized their lifetime egg production. In other
words, flies preferred to achieve maximum evolutionary
fitness rather than live as long as possible."

"In demonstrating the role protein plays in
determining both lifespan and reproduction, my
co-authors and I have united a body of apparently
conflicting work within a common framework and
provided a new platform for studying aging in all
organisms," Professor Simpson said.

According to Dr. Robert O. Young, a research scientist
at the pH Miracle Living Center, has stated, "proteins
are organizations of salt minerals, oxygen and water.
The primary element in the formation of protein is
nitrogen and oxygen which gives rise to phosphorus in
the creation of protein. The word equation is as follow:

Nitrogen + Oxygen <=> Phosphorus

Proteins can also been formed through the transformation
of sulfur in the following word equation:

Sulfur - Hydrogen <=> Phosphorus

Sulfur (S) is the element of transition to form
phosphorus (P). Sulfur (S) is a biological
transformation of nascent oxygen (O1) and/or
phosphorus (P).

O + O <=> S
S - H <=> P
F + O <=> P

"Sulfur (S) is found in glutathione and B vitamins
essential in maintaining the alkaline design of the
body."

http://www.phmiracleliving.com/glutathione.htm

"Sulfur (S) and Phosphorus (P) play an important role in
bone formation, gray matter, in the envelopes of neurons
and a constituent element of the nucleic acids."

"In the chain of DNA molecules a phosphoric group alternates
with deoxyribose. Phosphorus is thus one of the constituents
of deoxyribo-nucleic acid (DNA), which carries the
hereditary genetic code."

"Sulfur (S) and phosphorus (P) are major elements of life
and are linked in the relationship of life which allows
nature to go from one to the other in case of a deficiency."

Dr. Young further states, "the best sources of phosphorus
and sulfur are the green veggies, green fruits and
mineral salts from the sea, like broccoli, avocado,
green cabbage, sea vegetables, grasses and sea salt."

http://www.phmiracleliving.com/phruits.htm

"One of the most important reasons for not eating
protein and especially animal protein is to reduce
the acid load on the body. Animal proteins produce
toxic acidic residues of uric and nitric acid.
These acids from eating animal protein compromise
the delicate pH balance of the body fluids and sets
the stage for a variety of cancerous conditions," states
Dr. Young.

"The best diet for longevity, health, energy, fitness
and vitality is a diet that contains NO PROTEIN and
has a high concentration of chlorophyll, healthy
medium and long chain fats, alkaline water and all
the mineral salts or at least the 12 inorganic cell
or tissue salts," explains Dr. Young.

http://www.phmiracleliving.com/phlavor.htm

Dr. Young further states, "I call this way of
eating and drinking the COWS plan. Which is an
acronym that stands for:

C = chlorophyll
O = oil and oxygen
W = water that is clean and alkaline
S = salts that are whole and unprocessed."

Dr. Young is now offering a 4 ounce concentrated
liquid chlorophyll from organically grown alfalfa
for $19.95 a bottle. This concentrated liquid
chlorophyll has no preservatives, no sugars, no
alcohol added, like all other liquid chlorophyll
products on the market today. It is a freshly
juiced concentration of organic alfalfa that can
be added to any alkaline water. It is also great
for children. He currently offers in capsule in
powder a concentration of green fruits and vegetables.

http://www.phmiracleliving.com/phruits.htm

You can now pre-order this newly developed
Dr. Young, product by calling: 760-751-8321.
More aboutLow or No Protein Diet May Extend Life

Glutathione - The Master Acid Buster

Posted by luputtenan2 on Monday, February 25, 2008



The term glutathione is typically used as a
collective term to refer to the tripeptide
L-gamma-glutamyl-L-cysteinylglycine in both
its reduced and dimeric forms. Monomeric
glutathione is also known as reduced
glutathione and its dimer is also known
as oxidized glutathione, glutathione
disulfide and diglutathione.

In this monograph, reduced glutathione will
be called glutathione -- this is its common
usage by biochemists--and the glutathione
dimer will be referred to as glutathione
disulfide.

Glutathione is widely found in all forms of life
and plays an essential role in the health of
organisms, particularly aerobic organisms.

In animals, including humans, and in plants,
glutathione is the predominant non-protein
thiol and functions as a redox buffer, keeping
with its own SH groups those of proteins in a
reduced condition, among other antioxidant
activities.

Glutathione is present in tissues in concentrations
as high as one millimolar. Cysteine, the business
residue of glutathione, neither has the solubility
nor activity of glutathione at physiological alkaline
pH.

It appears that nature has built the cysteine
molecule into the glutathione tripeptide to
make the amino acid more soluble and allow it
to have redox buffering activity in a living
tissue environment.

Glutathione also plays roles in catalysis,
metabolism, signal transduction, gene expression
and apoptosis. It is a cofactor for glutathione
S-transferases, factors which are involved in
the detoxification of xenobiotics, including
carcinogenic genotoxicants, and for the
glutathione peroxidases, crucial
selenium-containing antioxidant factors.

It is also involved in the regeneration of
ascorbate from its oxidized form,
dehydroascorbate.

There are undoubtedly roles of glutathione that
are still to be discovered.

Glutathione is present in the diet in amounts
usually less than 100 milligrams daily.

Glutathione is not an essential nutrient since
it can be synthesized from the amino acids
L-cysteine, L-glutamate and glycine.

It is synthesized in two ATP-dependent steps:

First, gamma-glutamylcysteine is synthesized
from L-glutamate and cysteine via the factor
gamma-glutamylcysteine synthetase -- the rate
limiting step -- and second, glycine is added
to the C-terminal of gamma-glutamylcysteine
via the factor glutathione synthetase.

The liver is the principal site of glutathione
synthesis. In healthy tissue, more than 90%
of the total glutathione pool is in the reduced
form and less than 10% exists in the disulfide
form.

The glutathione disulfide reductase is the principal
molecule that maintains glutathione in its reduced
form. This latter molecule uses as its cofactor
NADPH (reduced nicotinamide adenine dinucleotide
phosphate). NADPH is generated by the oxidative
reaction in the pentose phosphate pathway.

The consequences of a functional glutathione
deficiency, which results in tissue oxidative
stress, can be seen in some pathological
conditions.

For example, those with glucose 6-phosphate
dehydrogenase deficiency produce lower amounts of
NADPH (Co-factor Q-1) and hence, lower amounts of
reduced glutathione. This condition is
characterized by a hemolytic anemia.

Conditions causing chronic glutathione deficiency
all result in hemolytic anemia, among other
pathological consequences. Oxidative stress caused
by glutathione deficiency results in fragile
erythrocyte (red blood cells) membranes.

Malaria-causing organisms (Plasmodia species)
do not like to feed on these sick erythrocytes.
That is about the only good news regarding this
situation.

Chronic functional glutathione deficiency is also
associated with immune disorders, an increased
incidence of malignancies, and in the case of HIV
dis-ease, probably accelerated pathogenesis of the
dis-ease.

Acute manifestations of functional glutathione
deficiency can be seen in those who have taken
an overdosage of acetaminophen (aspirin). This
results in depletion of glutathione in the
hepatocytes, leading to liver failure and death,
if not promptly treated.

Glutathione is an orphan drug for the treatment
of AIDS-associated cachexia. It is thought that
this disorder is due, in part, to oxidatively-stressed
and damaged enterocytes. There is some evidence that
although orally administered glutathione may not
be absorbed into the blood from the small intestine
to any significant extent, that it may be absorbed
into the enterocytes where it may help repair damaged
cells.

Glutathione in one form or another is the subject
of some medicinal chemistry research and many
clinical trials.

For example, an aerosolized form of glutathione
is being studied in AIDS and cystic fibrosis
patients.

Glutathione, the principal antioxidant of the
deep lung, appears to be diminished in those
with AIDS. Prodrugs of gamma-L-glutamyl-L-cysteine
are being evaluated as anticataract agents.

Glutathione (reduced) is known chemically as
N-(N-L-gamma-glutamyl-L-cysteinyl)glycine and
is abbreviated as GSH. Its molecular formula is
C10H17N3O6S and its molecular weight is 307.33
daltons.

Glutathione disulfide is also known as
L-gamma-glutamyl-L-cysteinyl-glycine disulfide
and is abbreviated as GSSG. Its molecular
formula is C20H32N6O12S2.

Many of the marketed glutathione dietary supplement
products are obtained from yeast fermentation, as is
the orphan drug. This is not the case with Dr.
Robert O. Young's, Young pHorever Glutathione which
is a glutathione extract from avocados.

www.phmiracleliving.com

Glutathione has antioxidant activity. It may
have detoxification, and immunomodulatory
activities, and may have beneficial effects
on sperm motility and in the protection against
noise-induced hearing loss.

Glutathione is the principal intracellular non
protein thiol and plays a major role in the
maintenance of the intracellular redox state.
It may be thought of as an intracellular redox
buffer to help maintain the alkaline design
of the cell.

Glutathione is a nucleophilic scavenger and an
electron donor via the sulfhydryl group of its
business residue, cysteine. Its reducing ability
maintains molecules such as ascorbate and proteins
in their reduced state.

Glutathione is also the cofactor for the
selenium-containing glutathione peroxidases,
which are major antioxidants. These antioxidants
detoxify peroxides, such as hydrogen peroxide
and other peroxides.

Another antioxidant activity of glutathione is
the maintenance of the antioxidant/reducing agent
ascorbate in its reduced state. This is accomplished
via glutathione-dependent dehydroascorbate reductase
which is comprised of glutaredoxin and protein
isomerase reductase. Glutathione may also react
with the reactive nitrogen species peroxynitrite
to form S-nitrosoglutathione.

Glutathione S-transferases (GSTs) consist of a
family of multifunctional factors that metabolize
a wide variety of electrophilic compounds via
glutathione conjunction.

GSTs are involved in the detoxification
of xenobiotic compounds and in the
protection against such degenerative
diseases as cancer.

The mechanism of these factors involves a
nucleophilic attack by glutathione on an
electrophilic substrate. The resulting glutathione
conjugates that form are more soluble than the
original substrates and thus more easily exported
from the cell.

The release of glutathione-S-conjugates
from cells is an ATP-dependent process mediated by
membrane glycoproteins belonging to the
multidrug-resistance protein (MRP) family.

Proteins of the MRP family are essential for the
transport of glutathione S-conjugates into the
extracellular space. They are also known as
glutathionine-S-conjugate pumps.

Absorption of orally administered glutathione has
been observed in some animals (mice, rats,
guinea pigs).

Oral glutathione has been demonstrated to reverse
age-associated decline in immune responsiveness
in mice.

In one study, glutathione was found to
enhance T-cell mediated responsiveness,
including delayed-type hypersensitivity
(DTH). The mechanism of this effect was
ascribed to the antioxidant activity of
glutathione.

Parenterally administered glutathione was
found to improve sperm motility in a small
human trial.

Again, the effect was thought to be due to the
antioxidant activity of this substance.

Noise-induced hearing loss is thought to be due
to oxidative stress. Intraperitoneal administration
of glutathione to guinea pigs was found to protect
against noise-induced hearing loss and once more,
the antioxidant activity of glutathione was thought
to account for this effect.

The pharmacokinetics of oral glutathionine in humans
are not well understood. It appears that in some
animals (mice, rats, guinea pigs), serum glutathione
levels do increase following its oral administration.

Though glutathione is undoubtedly a potent antioxidant.
There is preliminary evidence that it might eventually
prove to be useful in the management of some
cancers, atherosclerosis, diabetes, lung disorders,
noise-induced hearing loss, male infertility
and to help prevent or ameliorate various
toxicities.

It may also have some anti-viral (acid) activity.
Glutathione is an orphan drug for the treatment of
AIDS-associated cachexia.

RESEARCH SUMMARY

The use of glutathione in cancer treatment has
been two-fold. It has been investigated as an
antitumor agent in its own right and as a
chemoprotectant used to diminish the toxicities
of some cancer drugs.

In one animal study, glutathione produced
significant regression of aflatoxin-induced liver
cancers and significantly enhanced survival.

All rats exposed to aflatoxin but not given
glutathione died within 24 months of exposure to
the carcinogen, but 81% of the glutathione-treated
animals were still alive at the end of the 24
months. The researchers concluded that the
glutathione-effect noted in this study "strongly
suggests that this antioxidant merits further
investigation as a potential antitumor agent
in humans."

Human cancer studies, so far, have utilized
glutathione in a secondary role--principally to
protect against the toxicity of cisplatin.
Its role in this regard has been found effective
in several studies wherein it has been demonstrated
to diminish cisplatin-induced nephrotoxicity and
neurotoxicity.

Early research indicates that exogenous glutathione
may significantly inhibit platelet aggregation and
improve other hemostatic and hemorheological factors
in atherosclerotic patients. In other preliminary
clinical work, glutathione has been found to help
preserve renal function in patients who had coronary
artery bypass operations.

A glutathione nasal preparations has been helpful
in reversing the oxidant-antioxidant imbalance in
idiopathic pulmonary fibrosis, and it has helped
suppress lung epithelial surface inflammatory
cell-derived oxidants in patients with cystic fibrosis.

Similar nebulizing treatment has been given to HIV
patients to augment deficient glutathione levels
of the lower respiratory tract with the idea of
improving host defense in these immuno-compromised
individuals.

Glutathione has also been shown to enhance insulin
secretion in elderly subjects with impaired glucose
tolerance. There are some further preliminary
indications that glutathione might be helpful in
some with diabetes, but more research is needed
before any meaningful conclusions can be made.

In a double-blind, placebo-controlled study,
injected glutathione demonstrated a significant
positive effects on sperm motility and morphology
in infertile men. And, finally, in another study
that needs followup, glutathione exhibited
significant in vitro inhibition of herpes simplex
virus type 1 replication. It appears that the
mechanism of this effect is due to glutathione's
redox-modulating active. Some viral (acidic)
outfections, including HIV outfection, result
in oxidative stress which may be a major mechanism
of their pathogenesis, modulating oxidative stress
could be an antiviral (antiacid) maneuver.

Glutathione is an orphan drug for the treatment of
AIDS-associated cachexia.

Oral doses of up to 2000 milligrams daily are well
tolerated. There are no reports of adverse
reactions.

INTERACTIONS DRUGS

Cisplatin (Chemothearpy drug): Glutathione,
administered parenterally, may ameliorate some
of the adverse reactions of cisplatin.

OVERDOSAGE

There have been no reports of glutathione overdosage
in the literature.

DOSAGE AND ADMINISTRATION

Glutathione is available as a single ingredient
dietary supplement. Dosage ranges from 50 to
2000 milligrams daily. One teaspoon pr Young
pHorever Liquid Glutathione equals 430 milligrams.

http://www.phmiracleliving.com/glutathione.htm

HOW SUPPLIED

Liquid - one teaspoon of Young pHorever
Glutathione equals 430 milligrams.

To learn more about Young pHorever
Liquid Glutathione or to order go to:

http://www.phmiracleliving.com/glutathione.htm

SHOULD I ADD LIQUID GLUTATHIONE TO MY DIET?

Yes, as a major protectant from
dietary and lifestyle acidity.

LITERATURE

Anderson ME, Luo JL. Glutathione therapy:
from prodrugs to genes. Semin Liver Dis.
1998; 18:415-424.

Aw TW, Wierzbicka G, Jones DP. Oral glutathione
increases tissue glutathione in vivo.
Chem Biol Interact. 1991; 80:89-97.

Bains JS, Shaw CA. Neurodegenerative
disorders in humans: the role of glutathione
in oxidative stress-mediated neuronal death.
Brain Res Brain Res Rev. 1997; 25:335-358.

Borok Z, Buhl R, Grimes GJ, et al. Effect
of glutathione aerosol on oxidant-antioxidant
imbalance in ideopathic pulmonary fibrosis.
Lancet. 1991; 338:215-216.

Broquist HP. Buthionine sulfoximine, an
experimental tool to induce glutathionine
deficiency: elucidation of glutathionine
and ascorbate in their role as antioxidants.
Nutr Rev. 1992; 50:110-111.

Brown LA, Bai C, Jones DP. Glutathione
protection in aveolar type II cells from
fetal and neonatal rabbits. Am J Physiol.
1992; 262:L305-L312.

Cascinu S, Cordella L, Del Ferro E, et al.
Neuroprotective effect of reduced
glutathione on cisplatin-based chemotherapy
in advanced gastric cancer: a randomized
double-blind placebo-controlled study.
J Clin Oncol. 1995; 13:26-32.

Cheung P-Y, Wang W, Schulz R. Glutathione
protects against ischemia-perfusion injury
by detoxifying peroxynitrite. J Mol Cell
Cardiol. 2000; 32:1669-1678.

De Mattia G, Bravi MC, Laurenti O, et al.
Influence of reduced glutathione infusion
on glucose metabolism in patients with
non-insulin-dependent diabetes mellitus.
Metabolism. 1998; 47:993-997.

Exner R, Wessner B, Manhart N, Roth E.
Therapeutic potential of glutathione.
Wien Klin Wochenschr. 2000; 112:610-616.

Favilli F, Marraccini P, Iantomasi T,
Vincenzini MT. Effect of orally administered
glutathione levels in osme organs of rats:
role of specific transporters. Br J Nutr.
1997; 78:293-300.

Flagg EW, Coates RJ, Eley JW, et al. Dietary
glutathione intake in humans and the
relationship between intake and plasma
total glutathionine level. Nutr Canc.
1994; 21:33-46.

Furukawa T, Meydani SN, Blumberg JB. Reversal
of age-associated decline in immune
responsiveness by dietary glutathione
supplementation in mice. Mech Ageing
Dev. 1987; 38:107-117.

Griffith OW. Biologic and pharmacologic
regulation of mammalian glutathione
synthesis. Free Rad Biol Med. 1999;
27:922-935.

Hagen TM, Jones DP. Transepithelial transport
of glutathione in vascularly perfused small
intestine of rat. Am J Physiol. 1987;
252(5 Pt 1):G607-G613.

Hagen TM, Wierzbicka GT, Sillau AH, et al.
Bioavailability of dietary glutathione:
effect on plasma concentration.
Am J Physiol. 1990; 259(4 Pt 1):G524-G529.

Hayes JD, McLellan LI. Glutathione and
glutathione-dependent enzymes represent
a co-ordinately regulated defence against
oxidative stress. Free Rad Res. 1999;
31:273-300.

Hayes JD, Strange RC. Glutathione S-transferase
polymorphisms and their biological consequences.
Pharmacology. 2000; 61:154-166.

Hercbergs A, Brok-Simoni F, Holtzman F, et al.
Erythrocyte glutathione and tumor response to
chemotherapy. Lancet. 1992; 339:1074-1076.

Holroyd KJ, Buhl R, Borok Z, et al. Correction
of glutathione deficiency in the lower
respiratory tract of HIV seropositive
individuals by glutathione aerosol treatment.
Thorax. 1993; 48:985-989.

Hwang C, Sinskey AJ, Lodish HF. Oxidized
redox state of glutathione in the endoplasmic
reticulum. Science. 1992; 257:1496-1502.

Janaky R, Ogita K, Pasqualotta BA, et al.
Glutathione and signal transduction in the
mammalian CNS. J Neurochem. 1999; 73:889-902.

Lash LH, Hagen TM, Jones DP. Exogenous
glutathione protects intestinal epithelial
cells from oxidative injury. Proc Natl
Acad Sci USA. 1986; 83:4641-4645.

Lenzi A, Culasso F, Gandini L, et al.
Placebo-controlled, double-blind,
cross-over trial of glutathione therapy
in male infertility. Hum Reprod. 1993;
8:1657-1662.

Lenzi A, Picardo M, Gandini L, et al.
Glutathione treatment of dyspermia:
effect on the lipoperoxidation process.
Hum Reprod. 1994; 9:2044-2050.

Loguercio C, Di Pierro M. The role of
glutathione in the gastrointestinal
tract: a review. Ital J Gastroenterol
Hepatol. 1999; 31:401-407.

Lyons J, Rauh-Pfeiffer A, Yu YM, et al.
Blood glutathione synthesis rates in
healthy adults receiving a sulfur amino
acid-free diet. Proc Natl Acad Sci USA.
2000; 97:5071-5076.

Martensson J, Jain A, Meister A. Glutathione
is required for intestinal function.
Proc Natl Acad Sci USA. 1990; 87:1715-1719.

Meister A. On the antioxidant effects of
ascorbic acid and glutathionine. Biochem
Pharmacol. 1992; 44:1905-1915.

Murphy ME, Scholich H, Sies H. Protection
by glutathione and other thiol compounds
against the loss of protein thiols and
tocopherol homologs during microsomal
lipid peroxidation. Eur J Biochem. 1992;
210:139-146.

Nagasawa HT, Cohen JF, Holleschau AM,
Rathbun WB. Augmentation of human and
rat lenticular glutathione in vitro by
prodrugs of gamma-L-glutamyl-L-cysteine.
J Med Chem. 1996; 39:1676-1681.

Novi AM. Regression of aflatoxin B1-induced
hepatocellular carcinomas by reduced
glutathione. Science. 1981; 212:541-542.

Ohinataab Y, Yamasobac T, Schachta J,
Millera JM. Glutathione limits noise-induced
hearing loss. Hear Res. 2000; 146:28-34.

Palamara AT, Perno C-F, Ciriolo MR, et al.
Evidence for antiviral activity of glutathione:
in vitro inhibition of herpes simplex virus type
1 replication. Antiviral Res. 1995; 27:237-253.

Paolisso G, Giugliano D, Pizza G, et al.
Glutathione infusion potentiates glucose-induced
insulin secretion in aged patients with
impaired glucose tolerance. Diabetes Care.
1992; 15:1-7.

Roum JH, Borok Z, McElvaney NG, et al.
Glutathione aerosol suppresses lung
epithelial surface inflammatory cell-derived
oxidants in cystic fibrosis. J Appl Physiol.
1999; 87:438-443.

Samiec PS, Drews-Botsch C, Flagg EW, et al.
Glutathione in human plasma: decline in
association with aging, age-related macular
degeneration, and diabetes. Free Radic Biol
Med. 1998; 24:699-704.

Schmidinger M, Budinsky AC, Wenzel C, et al.
Glutathione in the prevention of cisplatin
induced toxicities. A prospectively randomized
pilot trial in patients with head and neck
cancer and non small cell lung cancer. Wien
Klin Wochenschr. 2000; 112:617-623.

Shaw CA, ed. Glutathione in the Nervous
System. London: Taylor and Francis; 1998.

Sies H. Glutathione and its role in cellular
functions. Free Rad Biol Med. 1999;
27:916-921.

Smyth JF, Bowman A, Perren T, et al.
Glutathione reduces the toxicity and
improves quality of life of women diagnosed
with ovarian cancer treated with cisplatin:
results of a double-blind, randomized trial.
Ann Oncol. 1997; 8:569-573.

Sternberg P Jr, Davidson PC, Jones DP, et al.
Protection of retinal pigment epithelium from
oxidative injury by glutathione and precursors.
Invest Opthalmol Vis Sci. 1993; 34:3661-3668.

Witschi A, Reddy S, Stofer B, Lauterburg BH.
The systemic availability of oral glutathione.
Eur J Clin Pharmacol. 1992; 43:667-669.
More aboutGlutathione - The Master Acid Buster

Curcumin Shows Promising Signs In Reducing Hypertension & Heart Enlargement

Posted by luputtenan2 on Sunday, February 24, 2008


Eating cur cumin, a natural ingredient in the
Young pHourer spice hunter turmeric (Garam Masala),
may dramatically reduce the chance of developing
heart failure, researchers at the Peter Munk Cardiac
Center of the Toronto General Hospital have
discovered.

http://www.phmiracleliving.com/spice_hunter.htm

In a study entitled, "Cur cumin prevents and reverses
murine cardiac hypertrophy," published in the February
edition of the Journal of Clinical Investigation,
researchers found when the herb is given orally to
a variety of mouse models with enlarged hearts
(hypertrophy), it can prevent and reverse hypertrophy,
restore heart function and reduce scar formation.

The healing properties of turmeric have been well
known in eastern cultures for some time. The herb
has been used in traditional Indian and Chinese
medicine to reduce scar formation. For example,
when there is a cut or a bruise, the home remedy
is to reach for turmeric powder because it can help
to heal without leaving a bad scar.

Unlike most natural compounds whose effects are
minimal, cur cumin works directly in the cell
nucleus by preventing abnormal unraveling of the
chromosome under stress, and preventing excessive
abnormal protein production.

"Cur cumin's ability to shut off one of the major
switches right at the chromosome source where the
enlargement and scarring genes are being turned
on is impressive," says Dr. Peter Liu, cardiologist
in the Peter Munk Cardiac Centre and Scientific
Director at the Canadian Institutes of Health
Research - Institute of Circulatory and Respiratory
Health. However Dr. Liu cautions that moderation
is important, "the beneficial effects of cur cumin
are not strengthened by eating more of it."

Dr. Liu, who holds the Heart and Stroke Foundation's
Polo Chair Professor in Medicine and Physiology at
the University of Toronto, says that since cur cumin
is a naturally occurring compound that is readily
available at a low cost, it might be a safe and
effective means of preventing heart failure in the
future.

"Whether you are young or old; male or female; the
larger your heart is, the higher your risk is for
developing heart attacks or heart failure in the
future. However, until clinical trials are done,
we don't recommend patients to take cur cumin routinely.
You are better off to take action today by lowering
blood pressure, reducing cholesterol, exercising and
healthy eating," says Dr. Liu.

If clinical trials of cur cumin support initial findings
of heart enlargement prevention, it may offer hope for
millions of patients with heart enlargement in a
relatively safe and inexpensive manner. Cur cumin-based
treatments are currently in clinical trials for
pancreatic and colon rectal cancer patients with
promising results.

Dr. Robert O. Young, a research scientist at the pH
Miracle Living Center, states, "cur cumin is a wonderful
buffer of metabolic and dietary acids that can lead
to hypertension and heart enlargement. The key to
eliminating hypertension and heart enlargement is to
reduce the levels are endogenous acids with better
lifestyle and dietary choices. One of those dietary
choices would definitely included the Young pHorever
cur cumin spice."

http://www.phmiracleliving.com/spice_hunter.htm
More aboutCurcumin Shows Promising Signs In Reducing Hypertension & Heart Enlargement

The Danger of Cell Phone Radiation

Posted by luputtenan2


Calling all cell phone users!

There is evidence of a new risk of cancer
from your mobile device.

A study, published in the American Journal of
Epidemiology, found that those who held a
handset to their ear for several hours a day
(an average of 22 hours per month) were 50-percent
more likely to develop a tumor in the parotid
gland.

The parotid gland is the largest of the salivary
glands. Historically, salivary gland cancer was
a very rare occurrence.

However, the proximity of the glands to the phone
has been of particular interest to scientists
concerned about the radio-frequency radiation
emitted from cell devices since their popularity
soared over a decade ago.

As part of an international Interphone Study,
Dr. Siegal Sadetzki, an epidemiologist at
Tel Aviv University, lead a team to investigate
nearly 500 people who had been diagnosed with
salivary gland tumors. The data was compared
to 1300 healthy subjects.

A significant part of the study is that it
was conducted in Israel.

“Unlike people in other countries, Israelis
were quick to adopt cell phone technology and
have continued to be exceptionally heavy users,”
Sadetzki said. “Therefore, the amount of exposure
to the radio frequency radiation found in this
study has been higher than in previous cell
phone studies.”

That may mean that the Israeli test shows the
results of cell phone use at an accelerated rate
compared to other populations.

Sadetzki does note that more information is
necessary to draw a definitive conclusion. However,
she also cautions people to ‘monitor their
conversations’ until the proof is in.

Children and young adults need to especially aware
since they are seen to be more vulnerable to the
effects of radiation. It has also been noted that
rural users may have a higher risk since their
mobile devices put off increased radiation to
compensate for weaker signals.

Dr. Robert O. Young, a research scientist at the
pH Miracle Living Center, states, "the parotid gland
is responsible for secreting sodium bicarbonate
to alkalize the food and liquids ingested. When
this gland is being radiated with cells phones
the pH of the saliva before ingesting of food or
drink and after ingesting of food or drink is
highly compromised. When the food and drink is
not alkalized by the alkaline secretions from
the parotid gland this can lead to a cancerous
condition. That is why I suggest maintaining
mouth pH at 7.2 or greater. This can be done
by drinking 4 grams of sodium bicarbonate in
8 ounces of 9.5 alkalized water. The additional
benefits of drinking sodium bicarbonate water
are as follows:

1) Increased pH of the extra-cellular body fluids.
2) Buffering of metabolic and dietary acids.
3) Protection against metabolic and dietary acids.
4) Buffering of HCL in the stomach that can cause
nausea, ulcers and stomach cancer.
5) Alkalizing of the food chyme in the small intestine.
6) Support of the stomach in its production of
sodium bicarbonate.
7) Helping to maintain the body's alkaline design and
thus preventing sickness and dis-ease."

To learn more about the many benefits of sodium
bicarbonate go to:

http://www.phmiracleliving.com/pHourSalts.htm

Dr. Young also suggests sympathetic resonance
technology to help protect against harmful cell
phone radiation. To learn more go to:

http://www.phmiracleliving.com/innerlink.htm
More aboutThe Danger of Cell Phone Radiation

Death By Vaccine

Posted by luputtenan2 on Saturday, February 23, 2008

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 antifungals will only poison the body leading to the one sickness and one disease - latent tissue acidosis and then death.

All vaccinations, antibiotics and antifungals are the acids of morbid fermentation of plant, animal and human matter and when ingested or injected, it only proves that you can poison the body and then hopefully live through it.

The day will soon come when scientists will proclaim that the use of vaccinations, antibiotics and antifungals were and 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 for yourself 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 'revaccination' 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.

1845 - 1849 J. Marion Sims, later hailed as the "father of gynecology," performs medical experiments on enslaved African women without anesthesia. These women would usually die of infection soon after surgery. Based on his belief that the movement of newborns' skull bones during protracted births causes trismus, he also uses a shoemaker's awl, a pointed tool shoemakers use to make holes in leather, to practice moving the skull bones of babies born to enslaved mothers (Brinker).


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.

1895
New York pediatrician Henry Heiman infects a 4-year-old boy whom he calls "an idiot with chronic epilepsy" with gonorrhea as part of a medical experiment ("Human Experimentation: Before the Nazi Era and After").

1896 Dr. Arthur Wentworth turns 29 children at Boston's Children's Hospital into human guinea pigs when he performs spinal taps on them, just to test whether the procedure is harmful (Sharav).

1906 Harvard professor Dr. Richard Strong infects prisoners in the Philippines with cholera to study the disease; 13 of them die. He compensates survivors with cigars and cigarettes. During the Nuremberg Trials, Nazi doctors cite this study to justify their own medical experiments (Greger, Sharav).

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 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 The head of French Public Health for the French Army said that germs alone were 'powerless to create an epidemic.'

1911 Dr. Hideyo Noguchi of the Rockefeller Institute for Medical Research publishes data on injecting an inactive syphilis preparation into the skin of 146 hospital patients and normal children in an attempt to develop a skin test for syphilis. Later, in 1913, several of these children's parents sue Dr. Noguchi for allegedly infecting their children with syphilis ("Reviews and Notes: History of Medicine: Subjected to Science: Human Experimentation in America before the Second World War").

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.

1913 Medical experimenters "test" 15 children at the children's home St. Vincent's House in Philadelphia with tuberculin, resulting in permanent blindness in some of the children. Though the Pennsylvania House of Representatives records the incident, the researchers are not punished for the experiments ("Human Experimentation: Before the Nazi Era and After").

1915 Dr. Joseph Goldberger, under order of the U.S. Public Health Office, produces Pellagra, a debilitating disease that affects the central nervous system, in 12 Mississippi inmates to try to find a cure for the disease. One test subject later says that he had been through "a thousand hells." In 1935, after millions die from the disease, the director of the U.S Public Health Office would finally admit that officials had known that it was caused by a niacin deficiency for some time, but did nothing about it because it mostly affected poor African-Americans. During the Nuremberg Trials, Nazi doctors used this study to try to justify their medical experiments on concentration camp inmates (Greger; Cockburn and St. Clair, eds.)

'Vaccinations, Not a Virus, Is Responsible for Spanish Flu - 1918'
Dr. Robert O. Young

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 vaccinal 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 antityphoid 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.

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.

1932-1972 The U.S. Public Health Service in Tuskegee, Ala. diagnoses 400 poor, black sharecroppers with syphilis but never tells them of their illness nor treats them; instead researchers use the men as human guinea pigs to follow the symptoms and progression of the disease. They all eventually die from syphilis and their families are never told that they could have been treated (Goliszek, University of Virginia Health System Health Sciences Library).

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.

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.

1939 In order to test his theory on the roots of stuttering, prominent speech pathologist Dr. Wendell Johnson performs his famous "Monster Experiment" on 22 children at the Iowa Soldiers' Orphans' Home in Davenport. Dr. Johnson and his graduate students put the children under intense psychological pressure, causing them to switch from speaking normally to stuttering heavily. At the time, some of the students reportedly warn Dr. Johnson that, "in the aftermath of World War II, observers might draw comparisons to Nazi experiments on human subjects, which could destroy his career" (Alliance for Human Research Protection).

(1941)

Dr. William C. Black infects a 12-month-old baby with herpes as part of a medical experiment. At the time, the editor of the Journal of Experimental Medicine, Francis Payton Rous, calls it "an abuse of power, an infringement of the rights of an individual, and not excusable because the illness which followed had implications for science" (Sharav).

An article in a 1941 issue of Archives of Pediatrics describes medical studies of the severe gum disease Vincent's angina in which doctors transmit the disease from sick children to healthy children with oral swabs (Goliszek).

Researchers give 800 poverty-stricken pregnant women at a Vanderbilt University prenatal clinic "cocktails" including radioactive iron in order to determine the iron requirements of pregnant women (Pacchioli).

1942 The Chemical Warfare Service begins mustard gas and lewisite experiments on 4,000 members of the U.S. military. Some test subjects don't realize they are volunteering for chemical exposure experiments, like 17-year-old Nathan Schnurman, who in 1944 thinks he is only volunteering to test "U.S. Navy summer clothes" (Goliszek).

Merck Pharmaceuticals President George Merck is named director of the War Research Service (WRS), an agency designed to oversee the establishment of a biological warfare program (Goliszek).

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.'

1944 - 1946 A captain in the medical corps addresses an April 1944 memo to Col. Stanford Warren, head of the Manhattan Project's Medical Section, expressing his concerns about atom bomb component fluoride's central nervous system (CNS) effects and asking for animal research to be done to determine the extent of these effects: "Clinical evidence suggests that uranium hexafluoride may have a rather marked central nervous system effect ... It seems most likely that the F [code for fluoride] component rather than the T [code for uranium] is the causative factor ... Since work with these compounds is essential, it will be necessary to know in advance what mental effects may occur after exposure." The following year, the Manhattan Project would begin human-based studies on fluoride's effects (Griffiths and Bryson).

The Manhattan Project medical team, led by the now infamous University of Rochester radiologist Col. Safford Warren, injects plutonium into patients at the University's teaching hospital, Strong Memorial (Burton Report).


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.

1945 Continuing the Manhattan Project, researchers inject plutonium into three patients at the University of Chicago's Billings Hospital (Sharav).

The U.S. State Department, Army intelligence and the CIA begin Operation Paperclip, offering Nazi scientists immunity and secret identities in exchange for work on top-secret government projects on aerodynamics and chemical warfare medicine in the United States ("Project Paperclip").

(1945 - 1955) In Newburgh, N.Y., researchers linked to the Manhattan Project begin the most extensive American study ever done on the health effects of fluoridating public drinking water (Griffiths and Bryson).

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.

1946 Continuing the Newburg study of 1945, the Manhattan Project commissions the University of Rochester to study fluoride's effects on animals and humans in a project codenamed "Program F." With the help of the New York State Health Department, Program F researchers secretly collect and analyze blood and tissue samples from Newburg residents. The studies are sponsored by the Atomic Energy Commission and take place at the University of Rochester Medical Center's Strong Memorial Hospital (Griffiths and Bryson).

(1946 - 1947) University of Rochester researchers inject four male and two female human test subjects with uranium-234 and uranium-235 in dosages ranging from 6.4 to 70.7 micrograms per one kilogram of body weight in order to study how much uranium they could tolerate before their kidneys become damaged (Goliszek).

Six male employees of a Chicago metallurgical laboratory are given water contaminated with plutonium-239 to drink so that researchers can learn how plutonium is absorbed into the digestive tract (Goliszek).

Researchers begin using patients in VA hospitals as test subjects for human medical experiments, cleverly worded as "investigations" or "observations" in medical study reports to avoid negative connotations and bad publicity (Sharav).

The American public finally learns of the biowarfare experiments being done at Fort Detrick from a report released by the War Department (Goliszek).

1947 Col. E.E. Kirkpatrick of the U.S. Atomic Energy Commission (AEC) issues a top-secret document (707075) dated Jan. 8. In it, he writes that "certain radioactive substances are being prepared for intravenous administration to human subjects as a part of the work of the contract" (Goliszek).

A secret AEC document dated April 17 reads, "It is desired that no document be released which refers to experiments with humans that might have an adverse reaction on public opinion or result in legal suits," revealing that the U.S. government was aware of the health risks its nuclear tests posed to military personnel conducting the tests or nearby civilians (Goliszek).

The CIA begins studying LSD's potential as a weapon by using military and civilian test subjects for experiments without their consent or even knowledge. Eventually, these LSD studies will evolve into the MKULTRA program in 1953 (Sharav).

(1947 - 1953) The U.S. Navy begins Project Chatter to identify and test so-called "truth serums," such as those used by the Soviet Union to interrogate spies. Mescaline and the central nervous system depressant scopolamine are among the many drugs tested on human subjects (Goliszek).

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 Based on the secret studies performed on Newburgh, N.Y. residents beginning in 1945, Project F researchers publish a report in the August 1948 edition of the Journal of the American Dental Association, detailing fluoride's health dangers. The U.S. Atomic Energy Commission (AEC) quickly censors it for "national security" reasons (Griffiths and Bryson).

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.

(1950 - 1953) The U.S. Army releases chemical clouds over six American and Canadian cities. Residents in Winnipeg, Canada, where a highly toxic chemical called cadmium is dropped, subsequently experience high rates of respiratory illnesses (Cockburn and St. Clair, eds.).

In order to determine how susceptible an American city could be to biological attack, the U.S. Navy sprays a cloud of Bacillus globigii bacteria from ships over the San Francisco shoreline. According to monitoring devices situated throughout the city to test the extent of infection, the eight thousand residents of San Francisco inhale five thousand or more bacteria particles, many becoming sick with pneumonia-like symptoms (Goliszek).

Dr. Joseph Strokes of the University of Pennsylvania infects 200 female prisoners with viral hepatitis to study the disease (Sharav).

Doctors at the Cleveland City Hospital study changes in cerebral blood flow by injecting test subjects with spinal anesthesia, inserting needles in their jugular veins and brachial arteries, tilting their heads down and, after massive blood loss causes paralysis and fainting, measuring their blood pressure. They often perform this experiment multiple times on the same subject (Goliszek).

Dr. D. Ewen Cameron, later of MKULTRA infamy due to his 1957 to1964 experiments on Canadians, publishes an article in the British Journal of Physical Medicine, in which he describes experiments that entail forcing schizophrenic patients at Manitoba's Brandon Mental Hospital to lie naked under 15- to 200-watt red lamps for up to eight hours per day. His other experiments include placing mental patients in an electric cage that overheats their internal body temperatures to 103 degrees Fahrenheit, and inducing comas by giving patients large injections of insulin (Goliszek).


1951 Theiler wins Nobel for work on yellow fever vaccine.

1951 The U.S. Army secretly contaminates the Norfolk Naval Supply Center in Virginia and Washington, D.C.'s National Airport with a strain of bacteria chosen because African-Americans were believed to be more susceptible to it than Caucasians. The experiment causes food poisoning, respiratory problems and blood poisoning (Cockburn and St. Clair, eds.).

(1951 - 1956) Under contract with the Air Force's School of Aviation Medicine (SAM), the University of Texas M.D. Anderson Cancer Center in Houston begins studying the effects of radiation on cancer patients -- many of them members of minority groups or indigents, according to sources -- in order to determine both radiation's ability to treat cancer and the possible long-term radiation effects of pilots flying nuclear-powered planes. The study lasts until 1956, involving 263 cancer patients. Beginning in 1953, the subjects are required to sign a waiver form, but it still does not meet the informed consent guidelines established by the Wilson memo released that year. The TBI studies themselves would continue at four different institutions -- Baylor University College of Medicine, Memorial Sloan-Kettering Institute for Cancer Research, the U.S. Naval Hospital in Bethesda and the University of Cincinnati College of Medicine -- until 1971 (U.S. Department of Energy, Goliszek).

American, Canadian and British military and intelligence officials gather a small group of eminent psychologists to a secret meeting at the Ritz-Carlton Hotel in Montreal about Communist "thought-control techniques." They proposed a top-secret research program on behavior modification -- involving testing drugs, hypnosis, electroshock and lobotomies on humans (Barker).

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).

1952 At the famous Sloan-Kettering Institute, Chester M. Southam injects live cancer cells into prisoners at the Ohio State Prison to study the progression of the disease. Half of the prisoners in this National Institutes of Health-sponsored (NIH) study are black, awakening racial suspicions stemming from Tuskegee, which was also an NIH-sponsored study (Merritte, et al.).

(1953 - 1974) The U.S. Atomic Energy Commission (AEC) sponsors iodine studies at the University of Iowa. In the first study, researchers give pregnant women 100 to 200 microcuries of iodine-131 and then study the women's aborted embryos in order to learn at what stage and to what extent radioactive iodine crosses the placental barrier. In the second study, researchers give 12 male and 13 female newborns under 36 hours old and weighing between 5.5 and 8.5 pounds iodine-131 either orally or via intramuscular injection, later measuring the concentration of iodine in the newborns' thyroid glands (Goliszek).

As part of an AEC study, researchers feed 28 healthy infants at the University of Nebraska College of Medicine iodine-131 through a gastric tube and then test concentration of iodine in the infants' thyroid glands 24 hours later (Goliszek).

1953 - 1957 Eleven patients at Massachusetts General Hospital in Boston are injected with uranium as part of the Manhattan Project (Sharav).

In an AEC-sponsored study at the University of Tennessee, researchers inject healthy two- to three-day-old newborns with approximately 60 rads of iodine-131 (Goliszek).

Newborn Daniel Burton becomes blind when physicians at Brooklyn Doctors Hospital perform an experimental high oxygen treatment for Retrolental Fibroplasia, a retinal disorder affecting premature infants, on him and other premature babies. The physicians perform the experimental treatment despite earlier studies showing that high oxygen levels cause blindness. Testimony in Burton v. Brooklyn Doctors Hospital (452 N.Y.S.2d875) later reveals that researchers continued to give Burton and other infants excess oxygen even after their eyes had swelled to dangerous levels (Goliszek, Sharav).

A 1953 article in Clinical Science describes a medical experiment in which researchers purposely blister the abdomens of 41 children, ranging in age from eight to 14, with cantharide in order to study how severely the substance irritates the skin (Goliszek).

The AEC performs a series of field tests known as "Green Run," dropping radiodine 131 and xenon 133 over the Hanford, Wash. site -- 500,000 acres encompassing three small towns (Hanford, White Bluffs and Richland) along the Columbia River (Sharav).

In an AEC-sponsored study to learn whether radioactive iodine affects premature babies differently from full-term babies, researchers at Harper Hospital in Detroit give oral doses of iodine-131 to 65 premature and full-term infants weighing between 2.1 and 5.5 pounds (Goliszek).


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 pathologyof encephalitis from vaccination is 'anaphlactic hypersensitivity'.

(1955 - 1957) In order to learn how cold weather affects human physiology, researchers give a total of 200 doses of iodine-131, a radioactive tracer that concentrates almost immediately in the thyroid gland, to 85 healthy Eskimos and 17 Athapascan Indians living in Alaska. They study the tracer within the body by blood, thyroid tissue, urine and saliva samples from the test subjects. Due to the language barrier, no one tells the test subjects what is being done to them, so there is no informed consent (Goliszek).

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 - 1957) U.S. Army covert biological weapons researchers release mosquitoes infected with yellow fever and dengue fever over Savannah, Ga., and Avon Park, Fla., to test the insects' ability to carry disease. After each test, Army agents pose as public health officials to test victims for effects and take pictures of the unwitting test subjects. These experiments result in a high incidence of fevers, respiratory distress, stillbirths, encephalitis and typhoid among the two cities' residents, as well as several deaths (Cockburn and St. Clair, eds.).

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 The U.S. military conducts Operation Plumbbob at the Nevada Test Site, 65 miles northwest of Las Vegas. Operation Pumbbob consists of 29 nuclear detonations, eventually creating radiation expected to result in a total 32,000 cases of thyroid cancer among civilians in the area. Around 18,000 members of the U.S. military participate in Operation Pumbbob's Desert Rock VII and VIII, which are designed to see how the average foot soldier physiologically and mentally responds to a nuclear battlefield ("Operation Plumbbob", Goliszek).

1957 - 1964 As part of MKULTRA, the CIA pays McGill University Department of Psychiatry founder Dr. D. Ewen Cameron $69,000 to perform LSD studies and potentially lethal experiments on Canadians being treated for minor disorders like post-partum depression and anxiety at the Allan Memorial Institute, which houses the Psychiatry Department of the Royal Victoria Hospital in Montreal. The CIA encourages Dr. Cameron to fully explore his "psychic driving" concept of correcting madness through completely erasing one's memory and rewriting the psyche. These "driving" experiments involve putting human test subjects into drug-, electroshock- and sensory deprivation-induced vegetative states for up to three months, and then playing tape loops of noise or simple repetitive statements for weeks or months in order to "rewrite" the "erased" psyche. Dr. Cameron also gives human test subjects paralytic drugs and electroconvulsive therapy 30 to 40 times, as part of his experiments. Most of Dr. Cameron's test subjects suffer permanent damage as a result of his work (Goliszek, "Donald Ewan Cameron").

In order to study how blood flows through children's brains, researchers at Children's Hospital in Philadelphia perform the following experiment on healthy children, ranging in age from three to 11: They insert needles into each child's femoral artery (thigh) and jugular vein (neck), bringing the blood down from the brain. Then, they force each child to inhale a special gas through a facemask. In their subsequent Journal of Clinical Investigation article on this study, the researchers note that, in order to perform the experiment, they had to restrain some of the child test subjects by bandaging them to boards (Goliszek).


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 The U.S. Atomic Energy Commission (AEC) drops radioactive materials over Point Hope, Alaska, home to the Inupiats, in a field test known under the codename "Project Chariot" (Sharav).

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 In response to the Nuremberg Trials, Yale psychologist Stanley Milgram begins his famous Obedience to Authority Study in order to answer his question "Could it be that (Adolf) Eichmann and his million accomplices in the Holocaust were just following orders? Could we call them all accomplices?" Male test subjects, ranging in age from 20 to 40 and coming from all education backgrounds, are told to give "learners" electric shocks for every wrong answer the learners give in response to word pair questions.. In reality, the learners are actors and are not receiving electric shocks, but what matters is that the test subjects do not know that. Astoundingly, they keep on following orders and continue to administer increasingly high levels of "shocks," even after the actor learners show obvious physical pain ("Milgram Experiment").

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.

1962 Researchers at Laurel Children's Center in Maryland test experimental acne antibiotics on children, continuing their tests after half of the young test subjects develop severe liver damage because of the experimental medication (Goliszek).

1963 The FDA begins requiring that a new pharmaceutical undergo three human clinical trials before it will approve it. From 1962 to 1980, pharmaceutical companies satisfy this requirement by running Phase I trials, which determine a drug's toxicity, on prison inmates, giving them small amounts of cash for compensation (Sharav).

1963 Chester M. Southam, who injected Ohio State Prison inmates with live cancer cells in 1952, performs the same procedure on 22 senile, African-American female patients at the Brooklyn Jewish Chronic Disease Hospital in order to watch their immunological response. Southam tells the patients that they are receiving "some cells," but leaves out the fact that they are cancer cells. He claims he doesn't obtain informed consent from the patients because he does not want to frighten them by telling them what he is doing, but he nevertheless temporarily loses his medical license because of it. Ironically, he eventually becomes president of the American Cancer Society (Greger, Merritte, et al.).

Researchers at the University of Washington directly irradiate the testes of 232 prison inmates in order to determine radiation's effects on testicular function. When these inmates later leave prison and have children, at least four have babies born with birth defects. The exact number is unknown because researchers never follow up on the men to see the long-term effects of their experiment (Goliszek).

(1963 - 1966) New York University researcher Saul Krugman promises parents with mentally disabled children definite enrollment into the Willowbrook State School in Staten Island, N.Y., a resident mental institution for mentally retarded children, in exchange for their signatures on a consent form for procedures presented as "vaccinations." In reality, the procedures involve deliberately infecting children with viral hepatitis by feeding them an extract made from the feces of infected patients, so that Krugman can study the course of viral hepatitis as well the effectiveness of a hepatitis vaccine (Hammer Breslow).

(1963 - 1971) Leading endocrinologist Dr. Carl Heller gives 67 prison inmates at Oregon State Prison in Salem $5 per month and $25 per testicular tissue biopsy in compensation for allowing him to perform irradiation experiments on their testes. If they receive vasectomies at the end of the study, the prisoners are given an extra $100 (Sharav, Goliszek).

Researchers inject a genetic compound called radioactive thymidine into the testicles of more than 100 Oregon State Penitentiary inmates to learn whether sperm production is affected by exposure to steroid hormones (Greger).

In a study published in Pediatrics, researchers at the University of California's Department of Pediatrics use 113 newborns ranging in age from one hour to three days old in a series of experiments used to study changes in blood pressure and blood flow. In one study, doctors insert a catheter through the newborns' umbilical arteries and into their aortas and then immerse the newborns' feet in ice water while recording aortic pressure.

In another experiment, doctors strap 50 newborns to a circumcision board, tilt the table so that all the blood rushes to their heads and then measure their blood pressure (Goliszek).

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 reshponse 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.

1964 - 1967 The Dow Chemical Company pays Professor Kligman $10,000 to learn how dioxin -- a highly toxic, carcinogenic component of Agent Orange -- and other herbicides affect human skin because workers at the chemical plant have been developing an acne-like condition called Chloracne and the company would like to know whether the chemicals they are handling are to blame. As part of the study, Professor Kligman applies roughly the amount of dioxin Dow employees are exposed to on the skin 60 prisoners, and is disappointed when the prisoners show no symptoms of Chloracne. In 1980 and 1981, the human guinea pigs used in this study would begin suing Professor Kligman for complications including lupus and psychological damage (Kaye).

1965 As part of a test codenamed "Big Tom," the Department of Defense sprays Oahu, Hawaii's most heavily populated island, with Bacillus globigii in order to simulate an attack on an island complex. Bacillus globigii causes infections in people with weakened immune systems, but this was not known to scientists at the time (Goliszek, Martin).

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.

1966 U.S. Army scientists drop light bulbs filled with Bacillus subtilis through ventilation gates and into the New York City subway system, exposing more than one million civilians, including women and children, to the bacteria (Goliszek).

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'

1967 The CIA places a chemical in the drinking water supply of the FDA headquarters in Washington, D.C. to see whether it is possible to spike drinking water with LSD and other substances (Cockburn and St. Clair, eds.).

In a study published in the Journal of Clinical Investigation, researchers inject pregnant women with radioactive cortisol to see if the radioactive material will cross the placentas and affect the fetuses (Goliszek).

The U.S. Army pays Professor Kligman to apply skin-blistering chemicals to Holmesburg Prison inmates' faces and backs, so as to, in Professor Kligman's words, "learn how the skin protects itself against chronic assault from toxic chemicals, the so-called hardening process," information which would have both offensive and defensive applications for the U.S. military (Kaye).

Professor Kligman develops Retin-A as an acne cream (and eventually a wrinkle cream), turning him into a multi-millionaire (Kaye).

Researchers paralyze 64 prison inmates in California with a neuromuscular compound called succinylcholine, which produces suppressed breathing that feels similar to drowning. When five prisoners refuse to participate in the medical experiment, the prison's special treatment board gives researchers permission to inject the prisoners with the drug against their will (Greger).

1968 Planned Parenthood of San Antonio and South Central Texas and the Southwest Foundation for Research and Education begin an oral contraceptive study on 70 poverty-stricken Mexican-American women, giving only half the oral contraceptives they think they are receiving and the other half a placebo. When the results of this study are released a few years later, it stirs tremendous controversy among Mexican-Americans (Sharav, Sauter).

1969 Experimental drugs are tested on mentally disabled children in Milledgeville, Ga., without any institutional approval whatsoever (Sharav).

Judge Sam Steinfield's dissent in Strunk v. Strunk, 445 S.W.2d 145 marks the first time a judge has ever suggested that the Nuremberg Code be applied in American court cases (Sharav).

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.

1970 Under order from the National Institutes of Health (NIH), which also sponsored the Tuskegee Experiment, the free childcare program at Johns Hopkins University collects blood samples from 7,000 African-American youth, telling their parents that they are checking for anemia but actually checking for an extra Y chromosome (XYY), believed to be a biological predisposition to crime. The program director, Digamber Borganokar, does this experiment without Johns Hopkins University's permission (Greger, Merritte, et al.).

1971 Stanford University conducts the Stanford Prison Experiment on a group of college students in order to learn the psychology of prison life. Some students are given the role as prison guards, while the others are given the role of prisoners. After only six days, the proposed two-week study has to end because of its psychological effects on the participants. The "guards" had begun to act sadistic, while the "prisoners" started to show signs of depression and severe psychological stress (University of New Hampshire).

An article entitled "Viral Infections in Man Associated with Acquired Immunological Deficiency States" appears in Federation Proceedings. Dr.. MacArthur and Fort Detrick's Special Operations Division have, at this point, been conducting mycoplasma research to create a synthetic immunosuppressive agent for about one year, again suggesting that this research may have produced HIV (Goliszek).


1972 British Journal of Psychiatry #120 reveals that 'psychotic disorders may be caused by viral infections.' (Ref: viruses induced by vaccines).

1973 An Ad Hoc Advisory Panel issues its Final Report on the Tuskegee Syphilis Study, writing, "Society can no longer afford to leave the balancing of individual rights against scientific progress to the scientific community" (Sharav).

1973 The field of genetic engineering is opened by advances in scientific research, making way for creation of recombinent 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.

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.'

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.

1977 The National Urban League holds its National Conference on Human Experimentation, stating, "We don't want to kill science but we don't want science to kill, mangle and abuse us" (Sharav).

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 The CDC begins experimental hepatitis B vaccine trials in New York. Its ads for research subjects specifically ask for promiscuous homosexual men. Professor Wolf Szmuness of the Columbia University School of Public Health had made the vaccine's infective serum from the pooled blood serum of hepatitis-infected homosexuals and then developed it in chimpanzees, the only animal susceptible to hepatitis B, leading to the theory that HIV originated in chimpanzees before being transferred over to humans via this vaccine.

A few months after 1,083 homosexual men receive the vaccine, New York physicians begin noticing cases of Kaposi's sarcoma, Mycoplasma penetrans and a new strain of herpes virus among New York's homosexual community -- diseases not usually seen among young, American men, but that would later be known as common opportunistic diseases associated with AIDS (Goliszek).

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.

1980 According to blood samples tested years later for HIV, 20 percent of all New York homosexual men who participated in the 1978 hepatitis B vaccine experiment are HIV-positive by this point (Goliszek).

The first AIDS case appears in San Francisco (Goliszek).


1981 The CDC acknowledges that a disease known as AIDS exists and confirms 26 cases of the disease -- all in previously healthy homosexuals living in New York, San Francisco and Los Angeles -- again supporting the speculation that AIDS originated from the hepatitis B experiments from 1978 and 1980 (Goliszek).

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).

1982 Thirty percent of the test subjects used in the CDC's hepatitis B vaccine experiment are HIV-positive by this point (Goliszek).

1985 A former U.S. Army sergeant tries to sue the Army for using drugs on him in without his consent or even his knowledge in United States v.. Stanley, 483 U.S. 669. Justice Antonin Scalia writes the decision, clearing the U.S. military from any liability in past, present or future medical experiments without informed consent (Merritte, et al..

1987 Philadelphia resident Doris Jackson discovers that researchers have removed her son's brain post mortem for medical study. She later learns that the state of Pennsylvania has a doctrine of "implied consent," meaning that unless a patient signs a document stating otherwise, consent for organ removal is automatically implied (Merritte, et al.).

(1988 - 2001) The New York City Administration for Children's Services begins allowing foster care children living in about two dozen children's homes to be used in National Institutes of Health-sponsored (NIH) experimental AIDS drug trials. These children -- totaling 465 by the program's end -- experience serious side effects, including inability to walk, diarrhea, vomiting, swollen joints and cramps. Children's home employees are unaware that they are giving the HIV-infected children experimental drugs, rather than standard AIDS treatments (New York City ACS, Doran).

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.

1990 The United States sends 1.7 million members of the armed forces, 22 percent of whom are African-American, to the Persian Gulf for the Gulf War ("Desert Storm"). More than 400,000 of these soldiers are ordered to take an experimental nerve agent medication called pyridostigmine, which is later believed to be the cause of Gulf War Syndrome -- symptoms ranging from skin disorders, neurological disorders, incontinence, uncontrollable drooling and vision problems -- affecting Gulf War veterans (Goliszek; Merritte, et al.).

The CDC and Kaiser Pharmaceuticals of Southern California inject 1,500 six-month-old black and Hispanic babies in Los Angeles with an "experimental" measles vaccine that had never been licensed for use in the United States. Adding to the risk, children less than a year old may not have an adequate amount of myelin around their nerves, possibly resulting in impaired neural development because of the vaccine. The CDC later admits that parents were never informed that the vaccine being injected into their children was experimental (Goliszek).

The FDA allows the U.S. Department of Defense to waive the Nuremberg Code and use unapproved drugs and vaccines in Operation Desert Shield (Sharav)..


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.

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 Columbia University's New York State Psychiatric Institute and the Mount Sinai School of Medicine give 100 males -- mostly African-American and Hispanic, all between the ages of six and 10 and all the younger brothers of juvenile delinquents -- 10 milligrams of fenfluramine (fen-fen) per kilogram of body weight in order to test the theory that low serotonin levels are linked to violent or aggressive behavior. Parents of the participants received $125 each, including a $25 Toys 'R' Us gift certificate (Goliszek).

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.

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.

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 breakdown dead bodies.

6) Peanuts and corn which produce exotoxins and mycotoxins.

7) All fermented foods including soy sauce.

8) Antibiotics which are mycotoxins.

9) Antifungals which are stronger mycotoxins.

10) All vaccinations which 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-fugal use, vaccination and an acidic lifestyle and diet.

1995 A 19-year-old University of Rochester student named Nicole Wan dies from participating in an MIT-sponsored experiment that tests airborne pollutant chemicals on humans. The experiment pays $150 to human test subjects (Sharav).

In the Mar. 15 President's Advisory Committee on Human Radiation Experiments (ACHRE), former human subjects, including those who were used in experiments as children, give sworn testimonies stating that they were subjected to radiation experiments and/or brainwashed, hypnotized, drugged, psychologically tortured, threatened and even raped during CIA experiments. These sworn statements include:

  • Christina DeNicola's statement that, in Tucson, Ariz., from 1966 to 1976, "Dr. B" performed mind control experiments using drugs, post-hypnotic injection and drama, and irradiation experiments on her neck, throat, chest and uterus. She was only four years old when the experiments started.
  • Claudia Mullen's testimony that Dr. Sidney Gottlieb (of MKULTRA fame) used chemicals, radiation, hypnosis, drugs, isolation in tubs of water, sleep deprivation, electric shock, brainwashing and emotional, sexual and verbal abuse as part of mind control experiments that had the ultimate objective of turning her, who was only a child at the time, into the "perfect spy." She tells the advisory committee that researchers justified this abuse by telling her that she was serving her country "in their bold effort to fight Communism."
  • Suzanne Starr's statement that "a physician, who was retired from the military, got children from the mountains of Colorado for experiments." She says she was one of those children and that she was the victim of experiments involving environmental deprivation to the point of forced psychosis, spin programming, injections, rape and frequent electroshock and mind control sessions. "I have fought self-destructive programmed messages to kill myself, and I know what a programmed message is, and I don?t act on them," she tells the advisory committee of the experiments' long-lasting effects, even in her adulthood (Goliszek).


President Clinton publicly apologizes to the thousands of people who were victims of MKULTRA and other mind-control experimental programs (Sharav).

President Clinton appoints the National Bioethics Advisory Committee (Sharav).

Justice Edward Greenfield of the New York State Supreme Court rules that parents do not have the right to volunteer their mentally incapacitated children for non-therapeutic medical research studies and that no mentally incapacitated person whatsoever can be used in a medical experiment without informed consent (Sharav).

1996 Professor Adil E. Shamoo of the University of Maryland and the organization Citizens for Responsible Care and Research sends a written testimony on the unethical use of veterans in medical research to the U.S. Senate's Committee on Governmental Affairs, stating: "This type of research is on-going nationwide in medical centers and VA hospitals supported by tens of millions of dollars of taxpayers money. These experiments are high risk and are abusive, causing not only physical and psychic harm to the most vulnerable groups but also degrading our society?s system of basic human values. Probably tens of thousands of patients are being subjected to such experiments" ("Testimony of Adil E. Shamoo, Ph.D.").

The Department of Defense admits that Gulf War soldiers were exposed to chemical agents; however, 33 percent of all military personnel afflicted with Gulf War Syndrome never left the United States during the war, discrediting the popular mainstream belief that these symptoms are a result of exposure to Iraqi chemical weapons (Merritte, et al.).

President Clinton issues a formal apology to the subjects of the Tuskegee Syphilis Study and their families (Sharav).

1997 n an experiment sponsored by the U.S. government, researchers withhold medical treatment from HIV-positive African-American pregnant women, giving them a placebo rather than AIDS medication (Sharav).

On Sept. 18, victims of unethical medical experiments at major U.S. research centers, including the National Institutes of Mental Health (NIMH) testify before the National Bioethics Advisory Committee (Sharav).

1999 Adil E. Shamoo, Ph.D. testifies on "The Unethical Use of Human Beings in High-Risk Research Experiments" before the U.S. House of Representatives' House Committee on Veterans' Affairs, alerting the House on the use of American veterans in VA Hospitals as human guinea pigs and calling for national reforms ("Testimony of Adil E. Shamoo, Ph.D.").

Doctors at the University of Pennsylvania inject 18-year-old Jesse Gelsinger with an experimental gene therapy as part of an FDA-approved clinical trial. He dies four days later and his father suspects that he was not fully informed of the experiment's risk (Goliszek)

During a clinical trial investigating the effectiveness of Propulsid for infant acid reflux, nine-month-old Gage Stevens dies at Children's Hospital in Pittsburgh (Sharav)..

2000 The U.S. Air Force and rocket maker Lockheed Martin sponsor a Loma Linda University study that pays 100 Californians $1,000 to eat a dose of perchlorate -- a toxic component of rocket fuel that causes cancer, damages the thyroid gland and hinders normal development in children and fetuses -- every day for six months. The dose eaten by the test subjects is 83 times the safe dose of perchlorate set by the State of California, which has perchlorate in some of its drinking water. This Loma Linda study is the first large-scale study to use human subjects to test the harmful effects of a water pollutant and is "inherently unethical," according to Environmental Working Group research director Richard Wiles (Goliszek, Envirnomental Working Group).

2001 On its website, the FDA admits that its policy to include healthy children in human experiments "has led to an increasing number of proposals for studies of safety and pharmacokinetics, including those in children who do not have the condition for which the drug is intended" (Goliszek).

In Higgins and Grimes v. Kennedy Krieger Institute The Maryland Court of Appeals makes a landmark decision regarding the use of children as test subjects, prohibiting non-therapeutic experimentation on children on the basis of "best interest of the individual child" (Sharav).

2002 President George W. Bush signs the Best Pharmaceuticals for Children Act (BPCA), offering pharmaceutical companies six-month exclusivity in exchange for running clinical drug trials on children. This will of course increase the number of children used as human test subjects (Hammer Breslow).

2003 Two-year-old Michael Daddio of Delaware dies of congestive heart failure. After his death, his parents learn that doctors had performed an experimental surgery on him when he was five months old, rather than using the established surgical method of repairing his congenital heart defect that the parents had been told would be performed.

The established procedure has a 90- to 95-percent success rate, whereas the inventor of the procedure performed on baby Daddio would later be fired from his hospital in 2004 (Willen and Evans, "Parents of Babies Who Died in Delaware Tests Weren't Warned").

2004 In his BBC documentary "Guinea Pig Kids" and BBC News article of the same name, reporter Jamie Doran reveals that children involved in the New York City foster care system were unwitting human subjects in experimental AIDS drug trials from 1988 to, in his belief, present times (Doran).

2005 In response to the BBC documentary and article "Guinea Pig Kids", the New York City Administration of Children's Services (ACS) sends out an Apr. 22 press release admitting that foster care children were used in experimental AIDS drug trials, but says that the last trial took place in 2001 and thus the trials are not continuing, as BBC reporter Jamie Doran claims.. The ACS gives the extent and statistics of the experimental drug trials, based on its own records, and contracts the Vera Institute of Justice to conduct "an independent review of ACS policy and practice regarding the enrollment of HIV-positive children in foster care in clinical drug trials during the late 1980s and 1990s" (New York City ACS).

Bloomberg releases a series of reports suggesting that SFBC, the largest experimental drug testing center of its time, exploits immigrant and other low-income test subjects and runs tests with limited credibility due to violations of both the FDA's and SFBC's own testing guidelines (Bloomberg).

In October 2005, the American Chemistry Council gave the EPA $2.1 million to study how children ranging from infancy to three years old ingest, inhale or absorb chemicals. Like IG Farben was for the German pharmaceutical companies of Nazi Germany, the American Chemistry Council acts much like a front group for chemical industry bigwigs like Bayer (which was incidentally also a member of IG Farben), BP, Chevron, Dow, DuPont, Exxon, Honeywell, 3M, Monsanto and Procter & Gamble. Studies have already proven that the chemicals made by these companies have long-term effects on children and adults. A short, two-year study like CHEERS would of course fail to reveal these long-term effects and the American Chemistry Council could then publicize these findings as "proof" that its chemicals were safe.

2006 2007 Merck begins pushing U.S. states to mandate the vaccination of teenage girls with Gardasil, a vaccine they claim prevents HPV, a sexually-transmitted virus. In February 2007, Texas Gov. Rick Perry -- who was revealed to have financial ties with Merck, the vaccine manufacturer -- mandates the vaccine in teenage girls (see http://www.NaturalNews.com/021572.html )..

A key Merck lobbyist named Mike Toomey, it turned out, had served as Gov. Rick Perry's chief of staff.

The Texas decision to mandate the vaccine was a notable and troubling milestone in public health policy because it is the first time a vaccine is mandated for a disease that cannot be contracted through casual contact in public schools. It also invoked "gunpoint medicine," or the threat of arrest at gunpoint for not agreeing to receive state-mandated injections.

The Gardasil vaccinations remain a grand medical experiment being performed on children because it is not yet known what the long-term side effects of the vaccination will be, nor whether the vaccinations will actually lower rates of cervical cancer as intended.

2007 Maryland's governor and public health officials, fed up with the unwillingness of over 2,000 parents to have their children vaccinated, invoke gunpoint medicine yet again by threatening the parents with arrest and up to 30 days of imprisonment if they don't submit their children to state-mandated vaccinations. The children and parents are later rounded up at a county courthouse, guarded by attack dogs and security personnel, while a district Judge oversees the mass injection of schoolchildren with vaccines that contain toxic mercury. (See http://www.NaturalNews.com/022242.html )

Present day: New Jersey mandates the mass vaccination of all children with four different vaccines, stripping away the health freedoms of parents and unleashing a mass medical experiment that exploits the bodies of children and enriches pharmaceutical companies while criminalizing parents who refuse to participate.

2008 A formal investigation has been launched by French authorities against two managers from drug companies GlaxoSmithKline and Sanofi Pasteur. A second investigation for manslaughter has also been opened against Sanofi Pasteur MSD.

The investigations are in response to allegations that the companies failed to fully disclose side effects from an anti-hepatitis B drug used between 1994 and 1998.

During this time, close to two-thirds of the French population, and almost all newborn babies, received a hepatitis B vaccine. The vaccination campaign was halted after concerns rose over the shot’s side effects.

Thirty plaintiffs, including the families of five people who died after the vaccination, have launched a civil action in the case against the drug companies. Source: Reuters February 1, 2008

For more information on viruses, bacteria, yeast and vaccines read Sick and Tired, Reclaim Your Inner Terrain, or A Second Thought About Viruses, Vaccines and the HIV AIDS Hypothesis, both by Dr. Robert O. Young.

I would also recommend reading Antione BeChamp's books, The Blood The Third Anatomical Element and The Origin of Organic Beings.

You can find these books at:

http://www.phmiracleliving.com/books.htm

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Brinker, Wendy. "James Marion Sims: Father Butcher." Seed Show.

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"Testimony of Adil E. Shamoo, Ph.D." News from the Joint Hearing on Suspension of Medical Research at West Los Angeles and Sepulveda VA Medical Facilities and Informed Consent and Patient Safety in VA Medical Research. 21 Apr. 1999.

University of New Hampshire. "Chronology of Cases Involving Unethical Treatment of Human Subjects." Responsible Conduct of Research.

University of Virginia Health System Health Sciences Library. "Bad Blood: The Tuskegee Syphilis Study." 2004.

U.S. Department of Energy. "Chapter 8: Postwar TBI-Effects Experimentation: Continued Reliance on Sick Patients in Place of Healthy "Normals." Advisory Committee on Human Radiation Experiments (ACHRE) Final Report.

Veterans Health Administration. Project 112/Project SHAD. May 26, 2005.

Willen, Liz and David Evans. "Doctor Who Died in Drug Test Was Betrayed by System He Trusted." Bloomberg. Nov. 2, 2005.

---. "Parents of Babies Who Died in Delaware Tests Weren't Warned." Bloomberg. Nov. 2, 2005
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