Dr NEIL MILLER
BOOK STUDY REVIEWS SUMMARY
Vaccine
Schedule Effects (p15-19
of Book)
Studies reviewed show: developed nations that require the most vaccines
tend to have the highest infant mortality rates; The U.S. requires the most
vaccinations and has the highest infant mortality rate.
developed nations
that require the least vaccines tend to have the lowest infant mortality rates.
Children who
had fewer vaccinations had fewer visits to doctor for respiratory disease and
less out-patient or emergency room visits.
Vaccines containing
Mercury Thimerosal (30 studies reviewed-p20-43)
Studies show
infants receiving vaccinations with thimerosal increase the risk of neurodevelopmental
effects; speech and sleep disorders; premature puberty; developmental delay;
ADHD; Autism and ASD; mental retardation; etc.
Premature
and Low Birth Weight Infants (21 studies starting p 211)
The
studies in this chapter provide strong evidence that vaccinating premature infants
can cause heart and respiratory conditions.
Premature
infants who are vaccinated are at higher risk o life
threatening apnea (SIDS).
When
premature infants are given several vaccines concurrently, the increased risk
is 4 times more likey to have increased
cardiovascular complications and 16 times more likely to have higher C-Reactive
protein level(inflammation).
Low birth
weight infants who are vaccinated are more likely to have adverse effects and
be rushed to the emergency room or be admitted to the hospital.
ALUMINUM
(26 studies p44-63 reviewed)
Aluminum is
neurotoxic and crosses the BBB into the brain and can remain there several years.
Animal studies show vaccinations can cause autoimmune effects and inflammatory adverse
effects. Studies show aluminum in vaccines causes nervous system harm in
children and adults.
There is
significant correlation between the number of aluminum
containing vaccines received and rate of autism spectrum disorders.
Countries
that require the most aluminum containing vaccines have the highest Autism
rates.
Injected aluminum
is much more harmful and does much more damage than dietary aluminum.
Aluminum
in vaccines can cause chronic fatigue, sleep disorders, cognitive problems,
memory problems, macrophagic myofascitis, muscle
weakness, and nerve demyelinating problems.
The FDA
has never shown that aluminum in vaccines is safe to be injected in children.
Influenza
(25 studies reviewed p44-64 of Miller Book Study Reviews)
(Strongly
recommended and promoted for all > 6 months)
Studies show: vaccination for seasonal flu increases susceptibility to
more virulent viruses.
People who
are naturally exposed to one strain of flu have increased immunity against
other strains,
The CDC
policy of vaccinating pregnant women is not supported by science.
Children
who get flu vaccine are significantly more likely to be hospitalized than
non-vaccinated children.
There is
no evidence that flu vaccines improve elderly death rates,
There is
no evidence vaccinating health care workers protects their patients, so
mandates not scientifically supported.
Health
authorities and Pharmaceuticals use unethical advertising scare campaigns to
promote vaccines not proven effective.
Health
Authorities and Pharmaceuticals exaggerate the danger of influenza and benefit
of vaccination.
Fku vaccines cause significant adverse effects.
Vaccinated
sometimes more likely to get flu and other infections than the unvaccinated.
Hand
washing and proper hygiene can be more effective for children than vaccination
at reducing infection risk.
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Pertussis
Vaccine and Pertussis Mutations
(27 studies
reviewed p85-104)
The studies
show; Old DPT Vaccine caused large number of deaths (SID) and significant
injuries, so new vaccine DPaT developed. But this
vaccine encourages evolutionary adaptations (mutations) and the number of
children who get whooping cough is increasing despite high vaccination rates. Cases
in vaccinated children have increased more than in unvaccinated children.
A study showed Baboons vaccinated for Pertussis were highly infectious
and spread the disease to other baboons. A study shows similar for children
vaccinated for Pertussis spread infection to others.
Pathogen
Evolution and Imperfect Vaccines (11 studies p105-112)
These
studies provide evidence that all vaccines are imperfect and cause incomplete
immunity. The studies confirm that
vaccines designed to reduce growth rate of pathogens in the host create conditions
that increase likelihood of more virulent strain and prevent eradication of the
disease.
Disease
causing organisms by nature tend to reduce virulence in the unvaccinated and
increase it in vaccinated. These studies provide evidence that imperfect
vaccines promote the evolution of more virulent strains that result in more
deadly infections. This adaptive behavior is favorable to the pathogen family
but detrimental to mass vaccination goals.
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Strain
Replacement (20 studies p113-126
Vaccines
that target only some strains of a pathogen can promote emergence of other
strains that can become more dominant and virulent. This has been the case with
Hib and Pneumonoccal Vaccine for example.
Human Papillomavirus
(HPV) (16 studies p127-138)
More than
100 strains and some can cause abnormal cell growth that can turn into cancer.
The HPV Vaccine developed is known to be linked to serious
adverse effects including autoimmune conditions, MS, ALS, GBS, paralysis,
convulsions, menstrual problems, CFS, pulmonary embolisms, etc. and death. Vaccine unlikely to reduce cancer in
countries where Pap smear is available.
Measles
and MMR Vaccine (11 studies p139-148)
Measles was
had by most children prior to 1960s and not serious in healthy children in
developed nations but can be more serious in malnourished or unhealthy children,
Studies now show childhood infections can have beneficial
effects and may be necessary to development of a healthy immune system. Studies
show that measles and mumps infections reduce the risk of heart attacks and
strokes. 3 studies here provide evidence of a link between MMR vaccine and
Autism, as well as autoimmune conditions and Cancer. MMR also documented to
cause deaths and other adverse effects, and more trips to hospital or emergency
room,
Chickenpox
and Shingles (24 studies p149-164)
Chickenpox is not a serious condition for healthy children,
and doctors in the past recommended exposing children at a conveniant
time to avoid having to deal with it at worse time. Studies show the virus is
protective against more serious conditions like cardiovascular disease. Chickenpox
vaccination reduces chickenpox cases but increases shingles cases which can be
more serious. Both the chickenpox and herpes zoster (shingles) vaccines are
seen to be associated with serious adverse effects including congestive heart
failure and pulmonary edema. Study shows
shingles vaccination increases the risk of arthritis and alopecia.
Polio,
Hepatitis B, and Rotavirus (20 studies p 165-171)
The
Polio, HepB, and Rotavirus vaccines all cause adverse
effects. They could never eradicate a viral disease. After a big polio vaccine
in India, there was a huge increase in non-viral acute flaccid paralysis which is as
serious as viral polio.
Studies
have found an increased risk of autoimmune conditions including MS, chronic
arthritis, and GBS after HepB vaccine. Studies have
found Rotavirus Vaccine increases risk of Intussusception and Kawasaki disease.
Allergies/MMR
/DPaT (14 study reviews p172-182)
Studies show
Children who contract measles have significantly less risk of allergies and
atopy than those who get MMR Vaccine.
Studies show
Children who contract chickenpox have significantly less risk of asthma and
allergies than those who get the vaccine.
Studies show
Children who get the Pertssis Vaccine have signicantly higher risk of asthma, hay ever, and food
allergies.
Children
who got their Pertussis Vaccine later had lower risk of asthma.
SEIZURES (13
studies p183-192)
These
studies provide strong evidence that Childhood Vaccines significantly increase
the risk of seizures.
Children
who got the Polio/Pertussis/HiB Vaccine had 8 times
higher risk of epilectic seizure within 24 hours.
Children
who got the MMR vaccine were up to 6 times more likely to have a convulsion
within 11 days.
DIABETES
(18 studies p-193-211)
These
medical studies provide strong evidence that Childhood Vaccines significantly
increase the risk of Type 1 Diabetes. (Hib, MMR, DPaT,
mumps,
A study
found that Children who got 4 Hib vaccinations were significantly more likely
to get Type 1 Diabetes by age 7,
Studies
show a child is significantly more likely to develop T1 Diabetes after receiving
MMR, HepB, and pertussis vaccines.
Epidemics
of Type II diabetes, obesity, and metabolic syndrome, ad inflammatory diseases
have been found to occur after vaccine campaigns.
The age
when vaccines are given can affect the likelihood of getting Type 1 Diabetes.
Thrombocytopenia
(10 studies p205-210)
The studies
in this chapter provide strong evidence that MMR vaccination increases the risk
of Thrombocytopenia (ITP).
Children
are up to 7 times more likely to get ITP within 6 weeks of MMR vaccination.
Children
are significantly more likely to get ITP after receiving pertussis, chickenpox, or HepA vaccines.
Severe
cases of ITP after vaccination can cause gastrointestinal and pulmonary hemorrhaging.
In one
study, ITP persisted for over 6 months in 10% of pediatric patients who
developed the condition.
Hexavalent
Vaccines (combined multiple vaccines) & Sudden Infant
Death Syndrome (SIDS)
(7 studies
starting p222)
The studies
in this chapter provide strong evidence that hexavalent vaccines significantly
increase the risk to infants.
One study
found that after the 4th hexavalent vaccine, infants are 23 times
more likely to die of SIDs than normal.
Another
study found that infants given one hexavalent vaccine
or 6 concurrent
vaccines are twice as likely to suffer SIDS in less than 2 weeks.
Autopsies
of infants who suffered SIDS after hexavalent vaccine found to have abnormal
neuropathology.
Cancer
and Vaccines and Beneficial Childhood Diseases (35 studies starting on p 228)
Women
with prior infections of mumps, measles, rubella, or chickenpox were
significantly less likely to get ovarian cancer, childhood leukemia, skin
cancer, brain cancer, and other types of cancer. Children who get Childhood
vaccines don’t get this protection.
Children
who get the MMR, pertussis, and HepB vaccines have a
significantly higher risk of leukemia.
Later born
children are less likely than first born children to get cancer (since they are
likely to get more infections).
The
studies in this chapter provide strong evidence that beneficial infections
provide protection against cancer while those who get childhood vaccines have
higher cancer risk.
VITAMIN A
& MEASLES (14 studies starting on p248 of Miller Vaccine Safety Study
Review Book)
Measles is
not a serious condition for healthy children, but can cause serious problems
for malnourished children or immune compromised deficient in vit A.
Vitamin A
is highly protective against complications and death from measles.
Severe
cases are mostly related to vit A deficiency.
AAP recommends
giving serious case patient over 1 year old 200,000 IU of Vit A on first day
and repeat the next day. Infants less than 6 months should get 50,000 IU each
of 2 days.
INFLUENZA
and Vit D (23 studies starting on p257 of Miller Study Review Book)
Ultraviolet
radiation from the sun induces vit D production in the skin. Sufficient Vit D
is required for a healthy immune system. Influenza incidence is affected by vit
D status.
In
developed countries 40% of pregnant women and 50% of infants have vit D
deficiency.
Studies
provide strong evidence that vit D supplementation reduces the incidence and
adverse effects of influenza and pneumonia.
Immune
system health is the most important factor in incidence and effects of influenza
and pneumonia.
