to Harris Coulter PhD, “Crib death” was so infrequent in the pre-vaccination
era that it was not even mentioned in statistics. It started to climb in
the 1950s with the spread of mass vaccinations. So much so it even acquired
a new name-“SIDS,” Sudden Infant Death Syndrome of unknown origin. The
medical establishment assures us that
is unrelated to vaccines which begs the question; How do you know its not
vaccines if it is of unknown origin? The three primary doses of DPT are
given at two, four and six months of age. Eighty-five per cent of SIDS
deaths occur from one to six months of age, with the peak incidence from two
to four months. Another coincidence?
In a recent study of SIDS,
monitored before and after vaccination. The data clearly showed
that vaccination caused an extraordinary increase in episodes where
breathing either nearly ceased or stopped completely. This is why it is so
important to have our babies sleep on their backs, if you plan on
vaccinating. It is easier for
them to breath. Another problem associated with breathing is Asthma.
Vaccinated children are shown to be five times more likely to become
afflicted with this serious respiratory ailment.
Dr. William Torch of the
University of Nevada School of Medicine did a study of 103 children who died
of SIDS. He found that more than two-thirds had been vaccinated with DPT
prior to death. Of these, 6.5% died within 12 hours; 13 % died within 24
hours; 26% died within 3 days; and 37, 61 and 70 % within 1,2,3 weeks
respectively. Anything that happens to a baby after four weeks is considered
The average time it takes for a vaccine to
dissipate in the body is 10-12 days.
Click here for
Dr Buttram's explanation. Even if
a baby dies immediately after a vaccination the cause of death will be
labeled SIDS. Here is one
example in the vaccine adverse reporting system.
The package insert on the
DTP vaccine states the following adverse events have occurred:
This was very clear to the
Japanese. They did not administer the DPT until their babies were two years
old. They had the lowest infant mortality rate in the world, until about
1981. This is when the Acellular Pertussis Vaccine, a “less toxic”
vaccine was made available to them.
In the U.S, the FDA fail to properly regulate the drug industry
after the less reactive DTaP vaccine was licensed for babies in 1996 . They
refused to recall the more toxic DPT vaccine and so it was injected into
American babies for six more years, just like mercury has been injected into
babies for six more years after the FDA told the drug companies to get it
out of vaccines.
Delay of DPT immunization until 2 years
of age in Japan had resulted in a dramatic decline in adverse side effects.
In the period of 1970-1974, when DPT vaccination was begun at 3 to 5 months
of age, the Japanese national compensation system paid out claims for 57
permanent severe damage vaccine cases, and 37 deaths. During the ensuing six
year period 1975-1980, when DPT injections were delayed to 24 months of age,
severe reactions from the vaccine were reduced to a total of eight with
three deaths. This represents an 85 to 90 percent reduction in severe cases
of damage and death." Raymond Obomsawin, M.D.
The DPaT cut adverse
reactions in half. It was 14 years before the U.S. finally licensed the less
reactive Acellular Pertussis Vaccine and this only in response to continued
pressure placed on the system by parents whose children were injured or died
after being injected with whole cell Pertussis vaccine DPT. IOM
Immunization Safety Review Session
Take a look at this study and be sure to read the last sentence.
Study on DPT
Reisinger a Veterinary Scientist, has worked more than forty-five years
studying this mechanism of death, and SIDS, in various mammalian species
including calves, foals, Rhesus Monkeys and human infants. He has found in
fact, that death is not sudden at all. He has proven
breastfeeding plays a major part in whether or not the baby will
thrive. He implicates E.Coli as the main culprit. This bacterium is
a protein-loving organism. The protein content of human breast milk is lower
than in any other mammal, and breast milk provides a hostile environment for
E. Coli. It also contains neutralizing factors as well. The protein content
of formula or any other milk supplement has a direct influence on the
numbers of E. Coli in the gut of the child or calf. Example: One bottle
of formula is enough to change a baby's gut micro flora dramatically, and it
takes two weeks of exclusive breast-feeding to return the gut to normal.
According to La Leche League, breastfeeding is nature’s vaccine. The
resistance to disease that human milk affords cannot be duplicated by any
number of vaccines. Breastfed babies are less likely to experience
Haemophilus Influence Type B, pneumonia and Meningitis. Large studies have
shown that infants who were not breastfed had two to three times greater
risk to die from SIDS than breastfed infants.
Because the natural antibodies are passed
on to the baby through the ‘white blood’ or breast milk, the formula
or soy formula
fed baby has little or no maternal antibodies, no protection of
gastrointestinal land respiratory mucosa. The half-life of this maternally
acquired antibody through the placenta is twenty days, so at two months old
the baby has only 1/8th of the antibodies he was born with, and at three
months, has less than 1/16th. The baby is unable to produce his own
protective antibodies for several more months. At this exceedingly
vulnerable time it is imperative that he not be subjected to undue stress.
His Reticulo Endothelial System, (which plays a major role in
detoxification of harmful substances) is at its limit with E.Coli. He may
be literally "up to the nose" in endotoxin (endotoxin is an integral part of
the cell wall of E.Coli and other gram-negative bacteria) but still "holding
his own.” When the ill-timed and ill-advised vaccination procedures are
inflicted upon the baby, it can be the straw that breaks the camel’s back.
The impact on the Reticulo-Endothelial
System is monstrous. Over just hours of time, small amounts of bacterial
endotoxin, not detoxified by a temporarily dysfunctional Reticulo-Endothelial
System, results in removal of blood platelets and fibrinogen from the
circulating blood. This pushes the Reticulo-Endothelial System past the
point of endurance, endotoxin slips through and out of the liver into the
blood stream, injuring platelets. The result is the release of relatively
large amounts of Serotonin from platelets into the blood plasma.
Serotonin is one of the brain's major neurotransmitters. It is the
biochemicals used by nerve cells to communicate with each other.
Serotonin affects the entire body. In the central nervous system, it
plays a role in sleep, appetite, memory, learning, temperature regulation,
mood, sexual behavior, cardiovascular function, muscle contraction,
endocrine regulation, and depression.
Some experiments demonstrated the increase of plasma Serotonin almost one
hundred fold after vaccination. Serotonin is associated with deep sleep. It
stimulates the Vagus Nerve to slow and even stop the heart. If death occurs
early in the course of this syndrome, it is due primarily to
Serotonin effect. Thimerosal
in the vaccine may also play a role. Take a look at this study:
Endotoxin has a direct
effect on cellular respiration. It interferes with metabolism of
mitochondria, which are tiny structures found in every cell, which uses a
molecular assembly line to convert food into the energy required for
cellular functions. Cells derive approximately 70 percent of their daily
energy needs from the mitochondria and
approximately 20 percent from another process
called glycolysis. High-energy tissues such as the
nervous system, skeletal
muscle and the heart are often compromised when there is
a crisis within
three and six hours, vascular capillary permeability has become more
substantial, and varying amounts of edema and hemorrhage by the passage of
blood cells through the unruptured vessel walls into the tissues may be
apparent. After six to eight hours or more, fibrin-platelet clots have
formed, and Disseminated Intravascular Coagulation (DIC) is present in
lungs, kidneys, and other organs and tissues. Depending on where the clot
settles decides the fate of the cells involved. For instance if it appears
in the eye, blindness may result. If it settles in the ear, deafness is the
organs are involved,
Dr. Reisinger describes this whole effect as being SIDS. The parents of
these children are sometimes charged with child abuse. Small hemorrhages in
are found in the brain along with clots that might form as the result of a
blow to the head. These
parents are not only devastated at the loss of their baby but wrongly
accused of hurting the child as well. The symptoms of “shaken
baby syndrome” are the same as what Dr Reisinger describes as endotoxemia.
endotoxin which is used as