The More Vaccines An Infant Receives In Its First Year, The Higher The Mortality Rate

The More Vaccines An Infant Receives In Its First Year, The Higher The Mortality Rate

Thursday, May 02, 2013


By Dave Mihalovic

How many babies have to die for Doctors to get it? Synergistic toxicity
is a well-known phenomenon where the combination of toxic substances can
be greater than the sum of its parts. Therefore, mixing two non-lethal
levels of chemicals inside a vaccine can lead to an extremely toxic
mixture. The medical community appears to gloss over this very pertinent
fact that appears to be progressively killing more infants every year.

“Synergistic toxicity” refers to the effect that when exposed to two
toxins, the toxicity level is far greater than the additive toxicity
levels of the two toxins. A good example demonstrating ‘synergistic
toxicity’ is a 1978 study on mice (Shubert et al. Combined Effects in
Toxicology — A Rapid systematic Testing Procedure: Cadmium, Mercury
& Lead. J. of Toxicology & Environmental Health 4:763, 1978).
The study took the amount of mercury salt that kills 1 in 100 mice and
1/20th of the amount of lead salt that kills 1 in 100 mice. When these
amounts of mercury salt and lead salt were administered, the synergistic
toxicity of these two toxins killed 100 in 100 mice.

It
is important to understand the concept of ‘synergistic toxicity’, as
research is increasingly showing that different toxins are typically
synergistic rather than additive in the human body. However when testing
is performed on a toxicity of a substance, the ‘level of harm’ is set
based on an assumption that the substance is the only toxin to which he
body is being exposed.

A study published in the Human and Experimental Toxicology journal has
found a direct statistical correlation between higher vaccine doses and
infant mortality rates. It is a confirmation that many anti-vaccine
advocates have long awaited and further establishes and adds to
preliminary evidence that vaccinations are toxic poisons having no place
in the human body. The study, Infant
mortality rates regressed against number of vaccine doses routinely
given: Is there a biochemical or synergistic toxicity?, was conducted by Gary S. Goldman and Neil Z. Miller who has been studying the dangers of vaccines for 25 years.




The infant mortality rate (IMR) is one of the most important indicators
of the socio-economic well-being and public health conditions of a
country. The US childhood immunization schedule specifies 26 vaccine
doses for infants aged less than 1 year–the most in the world–yet 33
nations have lower IMRs. Australia and Canada are a close 2nd and 3rd
respectively with 24 vaccine doses.

Some countries have IMRs that are less than half the US rate: Singapore,
Sweden, and Japan are examples. According to the Centers for Disease
Control and Prevention (CDC), “The relative position of the United
States in comparison to countries with the lowest infant mortality rates
appears to be worsening. ”

Many nations adhere to an agreed upon International Classification of
Diseases (ICD) for grouping infant deaths into 130 categories. Among the
34 nations analyzed, those that require the most vaccines tend to have
the worst IMRs. Thus, we must ask important questions: is it possible
that some nations are requiring too many vaccines for their infants and
the additional vaccines are a toxic burden on their health? Are some
deaths that are listed within the 130 infant mortality death categories
really deaths that are associated with over-vaccination? Are some
vaccine-related deaths hidden within the death tables?

“A single vaccine given to a six-pound newborn is the equivalent of
giving a 180-pound adult 30 vaccinations on the same day. Include in
this the toxic effects of high levels of aluminum and formaldehyde
contained in some vaccines, and the synergist toxicity could be
increased to unknown levels. Further, it is very well known that infants
do not produce significant levels of bile or have adult renal capacity
for several months after birth. Bilary transport is the major
biochemical route by which mercury is removed from the body, and infants
cannot do this very well. They also do not possess the renal (kidney)
capacity to remove aluminum. Additionally, mercury is a well-known
inhibitor of kidney function. “–Boyd Haley Ph.D.

How Many Deaths Are Necessary?
The end of 2011 was masked with sadness for Belgium parents Raphael
Sirjacobs & Beatrice Dupont, as their nine week old daughter Stacy
Sirjacobs lost her fight for life. Stacy died just one week after her first vaccinations
and left her twin sister Lesly behind. The twins received Prevenar, a
vaccine against meningitis and pneumonia, Infanrix Hexa, a six in one
vaccination for diphtheria, tetanus, polio, pertussis, hepatitis B and
Haemophilus type B, and finally the Rotarix, a preventive vaccine for
gastroenteritis. This means that these tiny vulnerable babies received a
staggering nine vaccines in one day, vaccines that may have caused one of them to die.

A government inquiry was launched in 2011 has found that polio vaccines
for infants funded by the Global Alliance for Vaccination and
Immunisation are causing deaths and disabilities in regional countries
including Pakistan. The report on The Express Tribune
also suggested suspending the mass polio campaign, including the
administration of pentavalent vaccines — a mixture of five vaccines
until an inquiry finds these vaccines safe for children. There is now
evidence that polio paralysis has also been a very common yet discreetly hidden side effect associated with polio vaccines.

When the first, injectable, polio vaccine was tested on 1.8 million
American children, within a few days they had a huge epidemic of
paralytic polio: in the vaccinated, their parents and other contacts.

On February 21, 2013, a one month-old baby girl died after receiving 5
vaccinations. Baby Ayushi Gupta died at the Maltibai Hospital, Thane,
West Mumbai in India just hours after receiving her vaccinations for Hepatitis B, DPT (diptheria, pertussis and tetanus) and oral pulse polio drops.

Vaccine Composition
This analysis calculated the total number of vaccine doses received by
children but did not differentiate between the substances, or quantities
of those sub-stances, in each dose. Common vaccine substances include
antigens (attenuated viruses, bacteria, toxoids), preservatives
(thimerosal, benzethonium chloride,2-phenoxyethanol, phenol), adjuvants
(aluminum salts), additives (ammonium sulfate, glycerin, sodium borate,
polysorbate 80, hydrochloric acid, sodium hydroxide, potassium
chloride), stabilizers (fetal bovine serum, monosodium glutamate, human
serumal bumin, porcine gelatin), antibiotics (neomycin, strep-tomycin,
polymyxin B), and inactivating chemicals (formalin, glutaraldehyde,
polyoxyethylene). For the purposes of this study, all vaccine doses were
equally weighted.





Using linear regression, the immunization schedules of these 34 nations
were examined and a correlation coefficient of 0.70 was found between
IMRs and the number of vaccine doses routinely given to infants. When
nations were grouped into five different vaccine dose ranges, 98.3% of
the total variance in IMR was explained by the unweighted linear
regression model. These findings demonstrate a counter-intuitive
relationship: nations that require more vaccine doses tend to have
higher infant mortality rate.


Mercury Still In 50 Percent of All Flu Vaccines
In 2009, eight out of ten H1N1 vaccines had thimerosal. For 2011/2012 flu vaccine season, three out of five FDA approved vaccines has thimerosal. This past year, the 2012/2013 season offered three out of six flu vaccines which contained thimerosal and were FDA approved.

If you have any doubts on the neurotoxic potential of thimerosal, please review the following scientific publications which document the adverse effects of mercury, merthiolate and ethyl mercury.

“One publication showed that combining mercury and lead both at LD1
levels caused the killing rate to go to 100% or to an LD100 level (12).
An LD1 level is where, due to the low concentrations, the mercury or the
lead alone was not very toxic alone (i.e. , killed less than 1% of rats
exposed when metal were used alone). The 100% killing, when addition of
1% plus 1% we would expect 2%, represents synergistic toxicity.
Therefore, mixing to non-lethal levels of mercury plus lead gave an
extremely toxic mixture! What this proves is that one cannot define a
“safe level of mercury” unless you absolutely know what others toxicants
the individual is being exposed to. The combined toxicity of various
materials, such as mercury, Thimerosal, lead, aluminum, formaldehyde,
etc. , is unknown. The effects various combinations of these toxicants
would have is also not defined except that we know they would be much
worse than any one of the toxicants alone. So how could the ADA take any
exception, based on intellectual considerations, to my contention that
combinations of Thimerosal and mercury could exacerbate the neurological
conditions identified with autism and AD? Autism and AD have clinical
and biological markers that correspond to those observed in patients
with toxic mercury exposure.

Why would the ADA take this position? I personally feel like I have
been in a ten-year argument with the town drunk on this issue. Facts
don’t count and data is only valid if it meets the pro-amalgam agenda.
The synergistic effects of mercury with many of the toxicants commonly
found in our environment make the danger unpredictable and possibly
quite severe, especially any mixture containing elemental mercury,
organic mercury and other heavy metal toxicants such as aluminum. ” ~
Boyd Haley

Dave Mihalovic is a Naturopathic Doctor who specializes in vaccine research, cancer prevention and a natural approach to treatment.

Source:-
http://www.naturalblaze.com/2013/05/the-more-vaccines-infant-receives-in.html