http://www.909shot.com/juvenilediabetes.htm

JUVENILE DIABETES AND VACCINATION:
NEW EVIDENCE FOR A CONNECTION
In the fall of 1997, the Centers for Disease
Control confirmed that the number of Americans living with diabetes has
skyrocketed in the past 40 years with a record sixfold increase in this chronic
disease since 1958. It is estimated that nearly 16 million Americans are
suffering with diabetes and 5 million more may have it but not know it.
Over the past four decades, intensive
national mass vaccination campaigns have dramatically increased vaccination
rates among American children who now are getting 34 doses of 10 different
viral and bacterial vaccines before they enter kindergarten. Recent published
data in the medical literature suggest increasing numbers of childhood vaccines
may be playing a role in the big jump in the number of cases of juvenile
diabetes.
What is diabetes?
The most frequent kind of diabetes is
diabetes mellitus, a chronic degenerative disease caused when the pancreas
either fails to produce a protein hormone called insulin or the body's cells
are resistant to the action of insulin. Without insulin, the body cannot
process and use glucose, a blood sugar which is a chief source of energy for
living organisms and is found in certain foods like fruit. If the body's cells
have become resistant to insulin, glucose cannot be moved from the blood to
cells in order to be transformed into energy.
There are two types of diabetes mellitus:
Type I, called insulin-dependent juvenile diabetes, and Type II, called
adult-onset diabetes.
Type I Diabetes - Type I diabetes, also called insulin-dependent
diabetes mellitus (IDDM), occurs mostly in children and young adults. Five to
10 percent of those diagnosed with diabetes are Type I diabetics. In Type I
diabetes, the body cannot produce insulin. This causes glucose to build up in
the bloodstream and be secreted from the body in the urine, leaving the body to
starve for energy because the body's cells cannot get the necessary nourishment
provided by glucose. Symptoms include excessive thirst, hunger, urination,
dehydration and often weight loss. Insulin injections must be taken daily to
keep blood glucose levels stable.
Type II Diabetes - Type II diabetes occurs primarily in middle age
and makes up 90 percent of all diagnosed cases of diabetes. The pancreas still
produces insulin in Type II diabetes but the body's cells are resistant to the
action of insulin and glucose is not absorbed properly by the cells. Obesity
and a family history of diabetes are risk factors for Type II diabetes.
Exercise, weight control, diet restrictions and medication can be used to
control Type II diabetes in many cases. Temporary insulin injections may also
be given.
Chronic Disease and High Medical Costs - Diabetes (Type I and Type II) is a chronic disease
that can become progressively debilitating for the individual as time goes on.
When uncontrolled or inadequately controlled, diabetes leads to blindness, loss
of hearing, heart and kidney disease, strokes, cataracts, nerve damage,
paralysis of the intestinal tract, gangrene requiring amputation of limbs and
death.
There have been estimates that some 125
million people worldwide have diabetes and that this number is expected to
double by the year 2025. According to the CDC, nearly 800,000 new cases of
diabetes are diagnosed in the US every year, with about 6 percent of the US
population now thought to have the disease.
Diabetes is the nation's seventh leading
cause of death and kills or is a co-factor in the deaths of some 200,000
Americans every year. The leading cause of acquired blindness, diabetes
contributes to about 24,000 new cases of acquired blindness in the US every
year. Half of all amputations performed in the US are caused by diabetes, which
means that about 54,000 amputations are diabetes-related. Diabetes is the
leading cause of kidney failure and the need for dialysis and kidney transplants.
Between 1980 and 1994, diabetes rose 33 percent among black Americans and 11
percent among white Americans.
Costs to cope with the growing epidemic of
diabetes are high. In 1992, it was estimated that diabetes cost the US $85
billion for medical treatment and an additional $47 billion for lost work time,
disability payments and premature death.
Old Reports, New Evidence of Vaccine
Connection - Doctors started making
reports in the medical literature as early as 1949 that some children injected
with pertussis (whooping cough) vaccine (now part of the DPT or DTaP shot) were
having trouble maintaining normal glucose levels in their blood. Lab research
has confirmed that pertussis vaccine can cause diabetes in mice.
As diabetes research progressed in the
1960's, 70's and 80's, there were observations that viral infections may be a
co-factor in causing diabetes. The introduction of live virus vaccines, such as
live MMR vaccine which is made from weakened forms of the live measles, mumps
and rubella viruses, has raised questions about whether live vaccine virus
could by a co-factor in causing chronic diseases such as diabetes.
One virus, the rubella virus, has already
been shown to be associated with diabetes. Babies infected with the rubella
virus in their mother's womb, who are born with congenitally acquired rubella
syndrome, often develop Type I diabetes. One 1980 study concluded that rubella
virus can infect pancreatic islet cells and that the infection can severely
reduce levels of secreted insulin. Another study in the 1980's demonstrated
that, after live rubella vaccination, the rubella virus can persist in the body
of a vaccinated person for many years.
Like rubella, mumps disease has been
strongly associated with the development of Type 1 diabetes. Like the rubella
virus, the mumps virus can infect pancreatic islet cells. And like the live
rubella vaccine, there are persistent reports in the medical literature that
some children develop diabetes after receiving live mumps vaccine.
An accumulation of scientific research today
suggests that Type 1 diabetes is an autoimmune disease. Autoimmunity is created
when the immune system malfunctions and attacks its own body. Genetic
predisposition and environmental factors (such as a viral infection) are
thought to be co-factors in the development of autoimmune disease, including
diabetes.
Because a vaccine artificially manipulates
the immune system in order to make it act as if it has recovered from and is
immune to a particular disease, some scientists are investigating whether
vaccination can be a co-factor in the development of autoimmune diseases like
diabetes. This research is particularly important for individuals who may have
a genetic predisposition to autoimmunity, such as those with a family history
of autoimmune disease.
New Evidence of Vaccine-Associated
Increases in Diabetes - Evidence of
a vaccination-diabetes connection has been strengthened since 1996 by the
epidemiologic investigation of J. Barthelow Classen, M.D., a former researcher
at the National Institutes of Health and the founder and CEO of Classen
Immunotherapies, Inc.. Dr. Classen is developing ways to prevent autoimmune
disease and maintains that one reason there is a growing epidemic of diabetes
in the world is because vaccines given to children at two months and older can
induce immune-mediated diabetes.
Classen has analyzed mass vaccination and
disease incidence data from foreign countries, which keep better records of
diabetes incidence than the U.S., as well as has conducted basic science research
experiments on mice and rats to support his argument. Beginning with lab
experiments, he demonstrated that 8 week old rats and mice injected with DPT
vaccine had a higher incidence of diabetes than those who were not injected
with DPT vaccine at 8 weeks old. Then he searched for evidence in existing
epidemiological data on human populations to suggest that injecting two month
old babies with vaccines causes an increased incidence in diabetes.
In the May 24, 1996 New Zealand Medical
Journal, Dr. Classen reported that there was a 60 percent increase in Type
I diabetes (juvenile diabetes) following a massive campaign in New Zealand from
1988 to 1991 to vaccinate babies six weeks of age or older with hepatitis B
vaccine. His analysis of a group of 100,000 New Zealand children prospectively
followed since 1982 showed that the incidence of diabetes before the hepatitis
B vaccination program began in 1988 was 11.2 cases per 100,000 children per
year while the incidence of diabetes following the hepatitis B vaccination
campaign was 18.2 cases per 100,000 children per year.
More Vaccines Equal More Diabetes - In the October 22, 1997 Infectious Diseases in
Clinical Practice, Classen presented more data further substantiating his
findings of a vaccine-diabetes connection. He reported that the incidence of
diabetes in Finland was stable in children under 4 years of age until the
government made several changes in its childhood vaccination schedule. In 1974,
130,000 children aged 3 months to 4 years were enrolled in a vaccine
experimental trial and injected with Hib vaccine or meningococcal vaccine.
Then, in 1976, the pertussis vaccine used in Finland was made stronger by
adding a second strain of bacteria. During the years 1977 to 1979, there was a
64 percent increase in the incidence of Type 1 diabetes in Finland compared to
the years 1970 to 1976.
In 1982, another vaccine was added to the
childhood vaccination schedule in Finland. Children aged 14 months to six years
were given the live MMR (measles-mumps-rubella) vaccine. This was followed by
the injection of 114,000 Finnish children aged 3 months and older with another
experimental Hib vaccine. In 1988, Finland recommended that all babies be
injected with the Hib vaccine.
The introduction of these new vaccines in
Finland were followed by a 62 percent rise in the incidence of diabetes in the
0 to 4 year old age group and a 19 percent rise of diabetes in the 5 to 9 year
old age group between the years 1980 and 1982 and 1987 and 1989. Classen
concluded:
"The net effect was the addition of
three new vaccines to the 0-4 year old age group and a 147 percent increase in
the incidence of IDDM [insulin dependent diabetes mellitus] , the addition of
one new vaccine to the 5-9 year olds and a rise in the incidence of diabetes of
40 percent, and no new vaccines added to the 10 to 14 year olds and a rise in
the incidence of IDDM by only 8 percent between the intervals 1970-1976 and
1990-1992. The rise in IDDM in the different age groups correlated with the
number of vaccines given."
Biological Mechanism Described - Classen says that when infants are given vaccines at
two months of age and older, some infants may already have a sub-clinical
inflammation of insulin secreting cells due to exposure to diabetes-inducing
viruses carried by the mother such as coxsackievirus B infections. When babies
with this sub-clinical inflammation are injected with vaccines, the existing
inflammation is made worse by the release of interferon and causes an
autoimmune state leading to immune mediated Type 1 diabetes later in childhood.
Classen's data shows there can be a 1 to 4 year latency between the time the
vaccines are given and Type 1 diabetes appears.
Classen, whose company has developed
pediatric immunization methods to prevent diabetes, believes that Type 1
diabetes and other autoimmune disorders can be prevented by vaccinating babies
immediately after birth. He points to a much lower incidence of Type 1 diabetes
in children in Sweden who were given BCG vaccine at birth compared to Swedish
children who were given BCG vaccine at two months of age, data which correlates
with experiments he conducted on mice and rodents he injected with BCG vaccine
at birth and two weeks of age. He also points to data from other countries such
as Ireland and Switzerland to make his case for vaccination at birth. Classen
maintains that when vaccines are given at birth, the infant's body releases
interferon which protects the child from being colonized with diabetes-inducing
viruses carried by the mother.
Vaccine Trials Flawed - Whether vaccination at birth will prevent
vaccine-associated autoimmunity such as diabetes is not as clear as Classen's
analysis of compelling data suggesting vaccines can be a co-factor in the
development of Type I diabetes in children. Without large, well designed case
controlled studies, his proposed solution to vaccinate at birth cannot be
confirmed.
In the meantime, Classen is critical of past
and current vaccine trials used by drug companies and the FDA to license
vaccines and used by the CDC to make mass vaccination policies. In conclusion,
he said:
"The results indicate that previous
vaccine trials are flawed because they are not designed to detect associations
between vaccination and autoimmune diseases, such as IDDM. Prospective clinical
trials are needed to further evaluate the effect of vaccines on IDDM."
NVIC Calls For Government Funding of
Independent Researchers - Although
more than $1 billion dollars is appropriated by Congress to federal health
agencies every year to develop, purchase and promote the mass use of vaccines
by American children, none of that money is used to fund independent vaccine
researchers to investigate vaccine-associated health problems like diabetes. In
fact, reputable researchers outside of government like Dr. Classen, who want to
do vaccine adverse event research, are not given government grants to do that
kind of research.
The National Vaccine Information Center
maintains that there is an inherent conflict of interest in allowing the same
health officials in federal agencies responsible for researching, developing,
regulating, making national policy for and promoting vaccines to also be in
control of monitoring vaccine reactions and evaluating health problems
associated with vaccines. There is a similar conflict of interest in relying
solely on scientific data supplied by drug companies, who make and sell
vaccines for a profit, to license vaccines safe for use by the public without
corroborating independent scientific data about the vaccine's safety.
"Health officials in federal agencies
have no accountability to anyone when it comes to setting priorities for how
our tax dollars are used when it comes to vaccine research," said NVIC
president and co-founder Barbara Loe Fisher. "They can choose to do
whatever they want to do with the money they get from Congress. And they choose
to ignore the mounting evidence that vaccines are playing a role in the current
epidemic of chronic disease, such as diabetes, in our society. Instead, our tax
money is used to create more vaccines to add to the mandatory vaccination
schedule for our children. There have never been and there are no plans to fund
large independent studies to back-up the scientific validity of the
government's current vaccine policies and independently confirm they are
safe."
[DailyNews/May2001/_private/footer.htm] ALL INFORMATION, DATA, AND MATERIAL CONTAINED, PRESENTED, OR
PROVIDED HERE IS FOR GENERAL INFORMATION PURPOSES ONLY AND IS NOT TO BE
CONSTRUED AS REFLECTING THE KNOWLEDGE OR OPINIONS OF THE PUBLISHER, AND IS NOT
TO BE CONSTRUED OR INTENDED AS PROVIDING MEDICAL OR LEGAL ADVICE. THE
DECISION WHETHER OR NOT TO VACCINATE IS AN IMPORTANT AND COMPLEX ISSUE AND
SHOULD BE MADE BY YOU, AND YOU ALONE, IN CONSULTATION WITH YOUR HEALTH CARE
PROVIDER.