Amy W's Final Vaccine Document

It is an often a repeated fallacy that there is no research that supports the
supposition that vaccines can and do cause autism or any other possible life
long debilitating side effects. This talking point is most often repeated by
medical personnel and public health officials who have simply never been
told that these studies exist. In some cases, those who are offered the
information refuse to read the information when it is offered to them. It is due
to this high degree of cognitive dissonance that these professionals insist that
vaccine injury is an uncommon event. This is the information i have attained
over the last four years of my extensive research. I have also added
information from my notes.
Let's start off with this recent article from the Journal of American Physicians
and Surgeons: "Although CDC recommends polio, hepatitis B, diphtheria, tetanus, pertussis,
rotavirus, Haemophilus in uenzae type B, and pneumococcal vaccines for
two-, four-, and six-month-old infants, this combination of eight vaccines
administered during a single physician visit was never tested for safety in
clinical trials. This is at odds with a CDC report that found that mixed
exposures to chemical substances and other stress factors, including
prescribed pharmaceuticals, may produce increased or unexpected
deleterious health e ects. This CDC report also noted that exposures to
mixed stressors can produce health consequences that are additive,
synergistic, antagonistic, or can potentiate the response expected from
individual component exposures.12 Thus, CDC is well aware that mixing
several pharmaceutical products increases the likelihood of synergistic
toxicity and unexpected adverse reactions....."
Also states-
" Our study showed that infants who receive several vaccines concurrently,
as recommended by CDC, are significantly more likely to be hospitalized or
die when compared with infants who receive fewer vaccines simultaneously.
It also showed that reported adverse e ects were more likely to lead to
hospitalization or death in younger infants.
These findings are so troubling that we expected major media outlets in

America to sound an alarm, calling for an immediate reevaluation of current
preventive health care practices. But 4 years after publication of our study,
this has not happened."
SOURCE- www.jpands.org/vol21no2/miller.pdf
This is a file of 1000 peer reviewed scientific studies.

https://drive.google.com/file/d/0B3mMkPwF1DUPckVEZ2JkMXV2ams/view?
pref=2&pli=1
124 medical research on vaccine and autism

http://www.scribd.com/mobile/doc/220807175
"Nations that require more vaccines tend to have higher infant mortality
rates"
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170075/
"There is no Federal requirement for informed consent relating to

immunization." http://www.cdc.gov/vaccines/imz-managers/laws/
All vaccine inserts in their entirety.

http://www.vaccinesafety.edu/package_inserts.htm
***ALUMINUM***
Aluminum is in the following vaccines given to minors:
DTaP, Pediarix (DTaP-Hepatitis B-Polio combination), Pentacel (DTaP-HIB-Polio
combination), Hepatitis A, Hepatitis B, Haemophilus influenzae B (HIB),
Human Papilloma Virus (HPV), and Pneumococcal vaccines
Aluminum (Al), the most commonly used vaccine adjuvant, is a

demonstrated neurotoxin and a strong immune stimulator. Hence, adjuvant Al
has the potential to induce neuroimmune disorders. When assessing adjuvant
toxicity in children, two key points ought to be considered: (i) children should
not be viewed as "small adults" as their unique physiology makes them much
more vulnerable to toxic insults; and (ii) if exposure to Al from only few
vaccines can lead to cognitive impairment and autoimmunity in adults, is it
unreasonable to question whether the current pediatric schedules, often
containing 18 Al adjuvanted vaccines, are safe for children?
http://www.ncbi.nlm.nih.gov/pubmed/22099159
Aluminum is an experimentally demonstrated neurotoxin and the most

commonly used vaccine adjuvant. Despite almost 90 years of widespread use
of aluminum adjuvants, medical science's understanding about their
mechanisms of action is still remarkably poor. There is also a concerning
scarcity of data on toxicology and pharmacokinetics of these compounds. In
spite of this, the notion that aluminum in vaccines is safe appears to be
widely accepted. Experimental research, however, clearly shows that
aluminum adjuvants have a potential to induce serious immunological
disorders in humans. In particular, aluminum in adjuvant form carries a risk
for autoimmunity, long-term brain inflammation and associated neurological
complications and may thus have profound and widespread adverse health
consequences.
INGESTION vs INJECTION"In healthy subjects, only 0.3% of orally administered aluminum is absorbed
via the GI tract, and the kidneys effectively eliminate aluminum from the
human body. Only when the GI barrier is bypassed, such as by intravenous
infusion or in the presence of advanced renal dysfunction, does aluminum
have the potential to accumulate. As an example, with intravenously infused
aluminum, 40% is retained in adults and up to 75% is retained in neonates.
[4]"
"If a significant aluminum load exceeds the body's excretory capacity, the
excess is deposited in various tissues, including bone, brain, liver, heart,
spleen, and muscle. This accumulation causes morbidity and mortality
through various mechanisms.[2]"
http://emedicine.medscape.com/article/165315-overview
"In adults, aluminum exposure can lead to apparently age-related

neurological deficits resembling Alzheimer's and has been linked to this
disease and to the Guamanian variant, ALS-PDC. Similar outcomes have been
found in animal models. In addition, injection of aluminum adjuvants in an
attempt to model Gulf War syndrome and associated neurological deficits
leads to an ALS phenotype in young male mice.
In young children, a highly significant correlation exists between the number
of pediatric aluminum-adjuvanted vaccines administered and the rate of
autism spectrum disorders. Many of the features of aluminum-induced
neurotoxicity may arise, in part, from autoimmune reactions, as part of the
ASIA syndrome."
http://www.ncbi.nlm.nih.gov/m/pubmed/23609067/
Abstract
"Immune challenges during early development, including those vaccineinduced, can lead to permanent detrimental alterations of the brain and
immune function. Experimental evidence also shows that simultaneous
administration of as little as two to three immune adjuvants can overcome
genetic resistance to autoimmunity. In some developed countries, by the time
children are 4 to 6 years old, they will have received a total of 126 antigenic
compounds along with high amounts of aluminum (Al) adjuvants through
routine vaccinations. According to the US Food and Drug Administration,
safety assessments for vaccines have often not included appropriate toxicity
studies because vaccines have not been viewed as inherently toxic. Taken
together, these observations raise plausible concerns about the overall safety
of current childhood vaccination programs. When assessing adjuvant toxicity
in children, several key points ought to be considered: (i) infants and children
should not be viewed as "small adults" with regard to toxicological risk as
their unique physiology makes them much more vulnerable to toxic insults;
(ii) in adult humans Al vaccine adjuvants have been linked to a variety of
serious autoimmune and inflammatory conditions (i.e., "ASIA"), yet children
are regularly exposed to much higher amounts of Al from vaccines than
adults; (iii) it is often assumed that peripheral immune responses do not

affect brain function. However, it is now clearly established that there is a
bidirectional neuro-immune cross-talk that plays crucial roles in
immunoregulation as well as brain function. In turn, perturbations of the
neuro-immune axis have been demonstrated in many autoimmune diseases
encompassed in "ASIA" and are thought to be driven by a hyperactive
immune response; and (iv) the same components of the neuro-immune axis
that play key roles in brain development and immune function are heavily
targeted by Al adjuvants. In summary, research evidence shows that
increasing concerns about current vaccination practices may indeed be
warranted. Because children may be most at risk of vaccine-induced
complications, a rigorous evaluation of the vaccine-related adverse health
impacts in the pediatric population is urgently needed."
"Anxiety-like behavior was more pronounced among mice immunized with

alum. In conclusion, herein we report that immunization with the HBVv
(hepatitis b vaccine) aggravated kidney disease in an animal model of SLE.
Immunization with either HBVv or alum affected blood counts, neurocognitive
functions and brain gliosis. Our data support the concept that different
component of vaccines may be linked with immune and autoimmune
mediated adverse events."
Aluminum hydroxide (which is in vaccines) injections lead to motor deficits

and motor neuron degeneration
Aluminum adjuvant linked to Gulf War illness induces motor neuron death in
mice.
"Aluminum-treated groups also showed significant motor neuron loss (35%)

and increased numbers of astrocytes (350%) in the lumbar spinal cord. The
findings suggest a possible role for the aluminum adjuvant in some
neurological features associated with GWI and possibly an additional role for
the combination of adjuvants."

" By applying Hill's criteria for establishing causality between exposure and
outcome we investigated whether exposure to Al (aluminum) from vaccines
could be contributing to the rise in ASD (autism spectrum disorders)
prevalence in the Western world. Our results show that: (i) children from
countries with the highest ASD prevalence appear to have the highest
exposure to Al from vaccines; (ii) the increase in exposure to Al adjuvants
significantly correlates with the increase in ASD prevalence in the United
States observed over the last two decades"
How aluminum, an intracellular ROS generator promotes hepatic and

neurological diseases: the metabolic tale
"Metal pollutants are a global health risk due to their ability to contribute to a
variety of diseases. Aluminum (Al), a ubiquitous environmental contaminant
is implicated in anemia, osteomalacia, hepatic disorder, and neurological
disorder. In this review, we outline how this intracellular generator of reactive
oxygen species (ROS) triggers a metabolic shift towards lipogenesis in
astrocytes and hepatocytes. This Al-evoked phenomenon is coupled to
diminished mitochondrial activity, anerobiosis, and the channeling of ketoacids towards anti-oxidant defense. The resulting metabolic
reconfiguration leads to fat accumulation and a reduction in ATP synthesis,
characteristics that are common to numerous medical disorders. Hence, the
ability of Al toxicity to create an oxidative environment promotes
dysfunctional metabolic processes in astrocytes and hepatocytes. These
molecular events triggered by Al-induced ROS production are the potential
mediators of brain and liver disorders.
http://link.springer.com/article/10.1007%2Fs10565-013-9239-0
"Repeated immunization with antigen causes systemic autoimmunity in mice

otherwise not prone to spontaneous autoimmune diseases. Overstimulation
of CD4 + T cells by repeated immunization with antigen led to the
development of a fully-matured autoantibody-inducing CD4 + T (aiCD4 + T)
cell which had undergone T cell receptor (TCR) revision and was capable of
inducing autoantibodies. The aiCD4 + T cell was induced by de novo TCR
revision but not by cross-reaction to immunizing antigen, and subsequently

overstimulated CD8 + T cells, driving them to become MHC class I-restricted,
antigen-specific cytotoxic T lymphocytes (CTL). These CTLs could be further
matured by antigen cross-presentation, after which they caused autoimmune
tissue injury akin to systemic lupus erythematosus (SLE). Autoimmune tissue
injury did not appear in CD8 + T cell-deficient mice. Further, inhibition of
antigen-cross presentation by treating with chloroquine abrogated the
generation of CTL and autoimmune tissue injury.
Conclusion:
"Systemic autoimmunity appears to be the inevitable consequence of overstimulating the hosts immune system by repeated immunization with
antigen, to the levels that surpass systems self-organized criticality."
http://www.jimmunol.org/cgi/content/meeting_abstract/184/1_MeetingAbstrac
ts/93.39
Autoimmunity and non-accidental injury in children

Abstract:
"Background: The Shaken Baby Syndrome conceived by Guthkeltch to explain
bruises, fractures, retinal and cerebral haemorrhage and encephalopathy in
children, called the triad, can be explained by an autoimmune reaction to
antigens in a genetically susceptible child.
Method: Children diagnosed as suffering from Non-accidental injuries were
investigated for evidence of immune response reactions following mandated
vaccination and childhood illnesses. Results: It was found in all the cases
reported here the response to antigenic stimulation damaged the Beta cells
in the Pancreas causing Hypoinsulinaemia which inhibited the cellular uptake
of Vitamin C resulting in liver dysfunction, failure of carboxylation of the
Vitamin K dependent proteins resulting in haemorrhages and fractures
associated with the triad. Conclusion: Fractures, retinal and subdural
haemorrhages and encephalopathy in children is an autoimmune response
to antigenic stimulation in a genetically susceptible individual. Common
antigens are the mandated vaccines, viral bacterial and parasitic infections. "
Interpretation
"In all four cases shown here there is evidence that hyperglycaemia followed
vaccination and hyperglycaemia implies hypoinsulinism, an autoimmune

disorder resulting from the destruction of the Beta cells of the pancreas.
Since insulin is required for the transfer of vitamin C into the cells the
intracellular vitamin C is reduced[12]. The resulting tissue scurvy
compromises the function of the Liver by inhibiting carboxylation of the
clotting and bone forming factors and is manifested as the signs and
symptoms of the triad. Both Dr Kalokerinos and Professor Clemetson
recommended giving the infant Vitamin C before vaccination but it would
seem more appropriate to do an intradermal skin test to test for sensitivity in
every case. Both were firmly of the view that a metabolic abnormality of
Vitamin C was the essential cause of the signs and symptoms of the alleged
Non-accidental injuries. "
Michael D Innis. Autoimmunity and Non-Accidental Injury in Children. Clinical
Medicine Research. Vol. 2, No. 3, 2013, pp. 40-44. doi:
10.11648/j.cmr.20130203.15
http://article.sciencepublishinggroup.com/pdf/10.11648.j.cmr.20130203.15.pd
f
***ENCEPHALITIS***
"Encephalitis is inflammation of the brain that occurs when a virus directly
infects the brain or when a virus, vaccine, or something else triggers
inflammation. The spinal cord may also be involved, resulting in a disorder
called encephalomyelitis."
" Encephalitis can occur in the following ways:

A virus directly infects the brain. A virus that caused an infection in the past
becomes reactivated and directly damages the brain. A virus or vaccine
triggers a reaction that makes the immune system attack brain tissue (an
autoimmune reaction)."
" Autoimmune encephalitis: After certain viral infections or vaccines, the
body's immune system sometimes attacks the layers of tissue that wrap
around nerve fibers (called the myelin sheath) in the brain and spinal cord
The attack occurs because proteins in myelin resemble those in the virus. As
a result, nerve transmission becomes very slow. The resulting disorder, called
acute disseminated encephalomyelitis, resembles multiple sclerosis except
that symptoms do not come and go as they do in multiple sclerosis. The
viruses most often involved include enteroviruses, Epstein-Barr virus,
hepatitis A or B virus, human immunodeficiency virus (HIV), and influenza
viruses."
http://www.merckmanuals.com/home/brain_spinal_cord_and_nerve_disorders/
brain_infections/encephalitis.html
The common immunogenic etiology of chronic fatigue syndrome: from

infections to vaccines via adjuvants to the ASIA syndrome.
Abstract:
Chronic fatigue syndrome (CFS) is characterized by unexplained fatigue that
lasts for at least 6 months with a constellation of other symptoms. Most cases
start suddenly, and are usually accompanied by a flu-like illness. It is a
symptom-based diagnosis of exclusion, the pathogenesis of which is
unknown. Studies have examined and hypothesized about the possible
biomedical and epidemiologic characteristics of the disease, including genetic
predisposition, infections, endocrine abnormalities, and immune dysfunction
and psychological and psychosocial factors. Recently, the AISA
(autoimmune/inflammatory syndrome induced by adjuvants) syndrome was
recognized, indicating the possible contribution of adjuvants and vaccines to
the development of autoimmunity.
Review of Vaccine Induced Immune Overload and the Resulting Epidemics of

Type 1 Diabetes and Metabolic Syndrome, Emphasis on Explaining the Recent
Accelerations in the Risk of Prediabetes and other Immune Mediated Diseases
Abstract
"There has been an epidemic of inflammatory diseases that has paralleled
the epidemic on iatrogenic immune stimulation with vaccines. Extensive
evidence links vaccine induced immune over load with the epidemic of type 1
diabetes. More recent data indicates that obesity, type 2 diabetes and other
components of metabolic syndrome are highly associated with immunization
and may be manifestations of the negative feedback loop of the immune
system reacting to the immune overload. The epidemic of

diabetes/prediabetes appears to be accelerating at a time when the
prevalence of obesity has stabilized, indicating that the negative feedback
system of the immune system has been over whelmed. The theory of vaccine
induced immune overload can explain the key observations that have
confounded many competing hypothesis. The current paper reviews the
evidence that vaccine induced immune overload explains the disconnect
between the increase in prediabetes and nonalcoholic fatty liver at a time
when the obesity epidemic is waning in children."
http://www.omicsonline.com/open-access/vaccine-induced-immune-overloadand-the-resulting-epidemics-of-type-diabetes-and-metabolic-syndrome-17470862.S1-025.php?aid=24058
Conclusions
"There are significantly elevated risks of primarily emergency room visits
approximately one to two weeks following 12 and 18 month vaccination.
Future studies should examine whether these events could be predicted or
prevented"
***INFLUENZA***
Marketing vaccine by marketing disease
Closer examination of influenza vaccine policies shows that although
proponents employ the rhetoric of science, the studies underlying the policy
are often of low quality, and do not substantiate officials claims. The vaccine
might be less beneficial and less safe than has been claimed, and the threat
of influenza appears overstated.
http://www.bmj.com/content/346/bmj.f3037
Effectiveness of trivalent inactivated influenza vaccine in influenza-related

hospitalization in children: a case-control study.
Using the Cochran-Mantel-Haenszel test for asthma status stratification,
there was a significant association between hospitalization in asthmatic
subjects and TIV (p = 0.001). TIV did not provide any protection against
hospitalization in pediatric subjects, especially children with asthma. On the
contrary, we found a threefold increased risk of hospitalization in subjects
who did get the TIV vaccine. This may be a reflection not only of vaccine
effectiveness but also the population of children who are more likely to get
the vaccine.
" The FluMist influenza vaccine strains replicate in the nasopharynx and can
be recovered and cultured from respiratory secretions of vaccinated
individuals (shed). The pattern and duration of shedding is important to
understand because with prolonged shedding at high titer there is a
theoretical risk of loss of attenuated phenotype, reassortment with wild-type
influenza virus during influenza season, and transmission of vaccine virus to
unvaccinated people, some of whom may be immunocompromised and/or at
risk for complications of live viral infections."
"In each age group, among subjects who shed, shedding was most often
observed on days 2-3 post vaccination. Among the population for whom
FluMist is currently approved for use, i.e., individuals 2-49 years of age (n =
443), vaccine virus titers did not exceed 1.5 log10 TCID50/mL after day 11,
though some individuals shed vaccine strain virus as late as day 28 postvaccination. "
http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProd
ucts/UCM259175.pdf
***HPV***
Clustering of cases of insulin dependent diabetes (IDDM) occurring three
years after hemophilus influenza B (HiB) immunization support causal
relationship between immunization and IDDM.
Conclusion
"We documented here the evidence of the potential of the HPV vaccine to
trigger a life-disabling autoimmune condition. The increasing number of
similar reports of post HPV vaccine-linked autoimmunity and the uncertainty
of long-term clinical benefits of HPV vaccination are a matter of public health
that warrants further rigorous inquiry."
Conclusions:
"These findings are consistent with the hypothesis that immunization with the
recombinant hepatitis B vaccine is associated with an increased risk of MS,
and challenge the idea that the relation between hepatitis B vaccination and
risk of MS is well understood."
http://www.neurology.org/content/63/5/838.abstract
***HEPB***
Conclusions:
"Hepatitis B vaccination does not generally increase the risk of CNS
inflammatory demyelination in childhood. However, the Engerix B vaccine
appears to increase this risk, particularly for confirmed multiple sclerosis, in
the longer term. Our results require confirmation in future studies."
" A majority of the ophthalmological complications seen following hepatitis B

vaccination consist of vision loss, optic neuritis, papillary edema, uveitis,
acute placoid pigment epitheliopathy and central vein occlusion. We present
a 9-year-old girl who was referred to our hospital with decrease in vision and
pain in the left eye a week after hepatitis B vaccination. A diagnosis of
vaccine-induced optic neuritis was made."
Conclusions:
Children vaccinated in infancy are at increased risk of hepatitis B virus
infection in the late teens
http://www.bmj.com/content/325/7364/569
"Acquired autoimmunity syndromes occur after viral vaccinations. Molecular

mimicry is involved in these phenomena as is the necessity for the presence
of two chemically complimentary antigens and an immunologic adjuvant. The
HLA pattern of the host is also an important factor. The example used to
explain these phenomena is demyelinating disease that follows hepatitis B
vaccination. The somatic antigen of the hepatitis B virus in the vaccine has
chemical complimentarity with the Epstein-Barr virus antigen in the vaccine
recipient. The Epstein-Barr virus shows molecular mimicry with human
myelin. The immunologic adjuvant is either present in the vaccine or
muramyl peptides in the individual who is vaccinated. Why more than one
type of autoimmune disease occurs is explained by the fact that specific
autoimmune T-cells have been shown to develop clones that attack multiple
human tissues."
***MMR***
*According to the CDC the greatest reported complication is loose stool with
measles.
Measles Complications Conditions Diarrhea - 8% reported
Otitis media - 7% reported
Pneumonia - 6% reported
Encephalitis - 0.1% reported
Seizures - 0.6-0.7% reported
Death - 0.2% reported
http://www.cdc.gov/vaccines/pubs/pinkbook/meas.html
The measles mortality rate had already dropped by over 98% before the
vaccine was even introduced. Thanks to better nutrition and hygiene, the
death rate was LESS THAN 1 in 100,000 before the measles vaccine came
out.
http://business.financialpost.com/2014/04/16/lawrence-solomon-the-untoldstory-of-measles/
Waning of Maternal Antibodies Against Measles, Mumps, Rubella, and

Varicella in Communities With Contrasting Vaccination Coverage
"Conclusions: Children of mothers vaccinated against measles and, possibly,

rubella have lower concentrations of maternal antibodies and lose protection
by maternal antibodies at an earlier age than children of mothers in
communities that oppose vaccination. This increases the risk of disease
transmission in highly vaccinated populations."
http://jid.oxfordjournals.org/content/early/2013/04/29/infdis.jit143.full
Abstract
An outbreak of nine cases of mumps was reported from a total of 97
vaccinated nursing students at two medical colleges in Thailand in 2010, 1626 days after administration of MMR vaccine containing the L-Zagreb mumps
strain. Symptoms ranged in severity from fever and parotid swelling to
orchitis. Clinical samples were obtained from seven patients and three were
suitable for further study. Sequencing confirmed that the SH gene of the
mumps virus in the unpassaged clinical specimens was identical to the LZagreb SH gene in the vaccine. Further analysis of the viral genome identified
nucleotide position 5170 as a novel mutation which corresponds to an amino
acid change in the fusion protein. This study provides another virologically
confirmed example of mumps resulting from the L-Zagreb vaccine strain.
POLIO: Symptoms
"Approximately 72% of persons infected with polio will have no symptoms.
About 24% of infected persons have minor symptoms, such as fever, fatigue,
nausea, headache, flu-like symptoms, stiffness in the neck and back, and
pain in the limbs, which often resolve completely. Fewer than 1% of polio
cases result in permanent paralysis of the limbs (usually the legs). Of those
paralyzed, 5-10% die when the paralysis strikes the respiratory muscles. The
death rate increases with increasing age."
http://www.cdc.gov/vaccines/vpd-vac/polio/in-short-both.htm
Limited and localized outbreak of newly emergent type 2 vaccine-derived

poliovirus in sichuan, china.
Furthermore, while India has been polio-free for a year, there has been a
huge increase in non-polio acute flaccid paralysis (NPAFP). In 2011, there
were an extra 47,500 new cases of NPAFP. Clinically indistinguishable from
polio paralysis but twice as deadly, the incidence of NPAFP was directly
proportional to doses of oral polio received. Though this data was collected
within the polio surveillance system, it was not investigated.
"Oral poliovirus vaccine Trivalent OPV contains live attenuated strains of all
three serotypes of poliovirus in a 10:1:3 ratio. The vaccine viruses are grown
in monkey kidney tissue culture (Vero cell line). The vaccine is supplied as a
single 0.5-mL dose in a plastic dispenser. The vaccine contains trace amounts
of neomycin and streptomycin. OPV does not contain a preservative.
Live attenuated polioviruses replicate in the intestinal mucosa and lymphoid
cells and in lymph nodes that drain the intestine. Vaccine viruses are
excreted in the stool of the vaccinated person for up to 6 weeks after a dose.
Maximum viral shedding occurs in the first 12 weeks after vaccination,
particularly after the first dose.
Vaccine viruses may spread from the recipient to contacts. Persons coming in
contact with fecal material of a vaccinated person may be exposed and
infected with vaccine virus."
http://www.cdc.gov/vaccines/pubs/pinkbook/downloads/polio.pdf
Breast milk makes rotavirus vaccine less effective

"We examined fecal shedding of pentavalent rotavirus vaccine (RV5) for 9

days following the first dose of vaccine in infants between 6 and 12 weeks of
age. Rotavirus antigen was detected by enzyme immunoassay (EIA), and
vaccine-type rotavirus was identified by nucleotide sequencing based on
genetic relatedness to the RV5 VP6 gene. Stool from 22 (21.4%) of 103
children contained rotavirus antigen-positive specimens on 1 postvaccination days. Rotavirus antigen was detected as early as post-vaccination
day 3 and as late as day 9, with peak numbers of shedding on postvaccination days 6 through 8. Vaccine-type rotavirus was detected in all 50
antigen-positive specimens and 8 of 8 antigen-negative specimens. Nine
(75%) of 12 EIA-positive and 1 EIA-negative samples tested culture-positive
for vaccine-type rotavirus. Fecal shedding of rotavirus vaccine virus after the
first dose of RV5 occurred over a wide range of post-vaccination days not
previously studied. These findings will help better define the potential for
horizontal transmission of vaccine virus among immunocompromised
household contacts of vaccinated infants for future studies"
" Vaccine-type rotavirus was detected in all 50 antigen-positive specimens

and 8 of 8 antigen-negative specimens. Nine (75%) of 12 EIA-positive and 1
EIA-negative samples tested culture-positive for vaccine-type rotavirus. Fecal
shedding of rotavirus vaccine virus after the first dose of RV5 occurred over a
wide range of post-vaccination days not previously studied."
These vaccines contain either trace or significant amounts of

thimerosal/mercury according to the FDA
DTaP: Tripedia,
Flu shots: Fluzone, Fluvirin, Afluria, FluLaval
DT
TD
TT
Meningococcal: Menomune A, C, AC, and A/C/W-135
INGESTION VS INJECTION- Mercury

"Intentional subcutaneous or intravenous injection of elemental mercury
results in toxicity similar to chronic inorganic mercury exposure, but can also
result in severe tissue damage that may require extensive surgical
debridement. On the contrary, ingestion of elemental mercury is generally
benign and as there is almost no absorption of this form from the GI tract. "
http://www.calpoison.org/hcp/2011/callusvol9no1.htm
Abstract
" Thimerosal generates ethylmercury in aqueous solution and is widely used
as preservative. We have investigated the toxicology of Thimerosal in normal
human astrocytes, paying particular attention to mitochondrial function and
the generation of specific oxidants. We find that ethylmercury not only
inhibits mitochondrial respiration leading to a drop in the steady state
membrane potential, but also concurrent with these phenomena increases
the formation of superoxide, hydrogen peroxide, and Fenton/Haber-Weiss
generated hydroxyl radical. These oxidants increase the levels of cellular
aldehyde/ketones. Additionally, we find a five-fold increase in the levels of
oxidant damaged mitochondrial DNA bases and increases in the levels of
mtDNA nicks and blunt-ended breaks. Highly damaged mitochondria are
characterized by having very low membrane potentials, increased
superoxide/hydrogen peroxide production, and extensively damaged mtDNA
and proteins. These mitochondria appear to have undergone a permeability
transition, an observation supported by the five-fold increase in Caspase-3
activity observed after Thimerosal treatment."
Abstract
"Thimerosal, an organomercurial added as a preservative to some vaccines,
is a suspected iatrogenic factor, possibly contributing to paediatric
neurodevelopmental disorders including autism. We examined the effects of
early postnatal administration of thimerosal (four i.m. injections, 12 or 240 g

THIM-Hg/kg, on postnatal days 7, 9, 11 and 15) on brain pathology in Wistar
rats. Numerous neuropathological changes were observed in young adult rats
which were treated postnatally with thimerosal. They included: ischaemic
degeneration of neurons and "dark" neurons in the prefrontal and temporal
cortex, the hippocampus and the cerebellum, pathological changes of the
blood vessels in the temporal cortex, diminished synaptophysin reaction in
the hippocampus, atrophy of astroglia in the hippocampus and cerebellum,
and positive caspase-3 reaction in Bergmann astroglia. These findings
document neurotoxic effects of thimerosal, at doses equivalent to those used
in infant vaccines or higher, in developing rat brain, suggesting likely
involvement of this mercurial in neurodevelopmental disorders."
Maternal transfer of mercury to the developing embryo/fetus: is there a safe

level?
This study focused on standardized embryonic and fetal Hg exposures via
primary exposure to the pregnant mother of two common Hg sources (dietary
fish and parenteral vaccines). Data demonstrated that Hg exposures,
particularly during the first trimester of pregnancy, at well-established
dose/weight ratios produced severe damage to humans including death. . In
light of research suggestive of a mercuric risk factor for childhood conditions
such as tic disorders, cerebral palsy, and autism, it is essential that Hg
advisories account for secondary prenatal human exposures.
http://www.tandfonline.com/doi/full/10.1080/02772248.2012.724574
Conclusions:
" High blood mercury level was associated with ADHD. Whether the
relationship is causal requires further studies."
http://www.ncbi.nlm.nih.gov/pubmed/?term=17177150
" Varicella vaccination is less effective than the natural immunity that existed
in prevaccine communities. Universal varicella vaccination has not proven to
be cost-effective as increased HZ morbidity has disproportionately offset cost
savings associated with reductions in varicella disease. Universal varicella
vaccination has failed to provide long-term protection from VZV disease."
Varicella Zoster Virus (shingles vaccine) DNA at Inoculation Sites and in Saliva
After Zostavax Immunization
Abstract:
"Analysis of 36 individuals over age 60 years who were immunized with
Zostavax revealed varicella zoster virus (VZV) DNA in swabs of skin
inoculation sites obtained immediately after immunization in 18 (50%) of 36
subjects (copy number per nanogram of total DNA, 28 to 2.1 10 6 ) and in
saliva collected over 28 days in 21 (58%) of 36 subjects (copy number, 20 to
248). Genotypic analysis of DNA extracted from 9 random saliva samples
identified vaccine virus in all instances. In some immunized individuals over
age 60, vaccine virus DNA is shed in saliva up to 4 weeks."
Results:
" No saliva specimen collected immediately before immunization contained
VZV DNA. During the first week after immunization, VZV DNA was detected in
saliva of 21 (58%) of 36 subjects (13 men and 8 women). During the 28-day
study period, VZV DNA was found in 11 (31%) of 36 subjects (5 men and 6
women) at day 14, in 10 (28%) of 36 subjects (6 men and 4 women) at day
21, and in 2 (6%) of 36 subjects (1 man and 1 woman) at day 28. Figure 1
shows the percent of immunized subjects who shed VZV DNA during the 28day study period. VZV DNA copy numbers per nanogram of total DNA ranged
from 20 to 248 (Table 1). Genotypic analysis of DNA from 9 random saliva
samples revealed vaccine virus DNA in all instances (Table 1, bold); wild-type
VZV DNA was not detected. In 15 (42%) of 36 vaccine recipients (6 men, 9
women), VZV DNA was not detected in saliva at any time during the 28-day
study period."
http://jid.oxfordjournals.org/content/203/11/1542.long
" Pertussis can still be found in a fifth of school age children who present in
primary care with persistent cough and can cause clinically significant cough
in fully vaccinated children."
Unvaccinated children do not significantly contribute to whooping cough

outbreaks
" Our unvaccinated and undervaccinated population did not appear to
contribute significantly to the increased rate of clinical pertussis. Surprisingly,
the highest incidence of disease was among previously vaccinated children
aged 812 years. We sought to examine the factors that resulted in this
peak."
"Of the 132 individuals (77.2%) aged 18 years at time of illness, 81% were
fully vaccinated, 11% were undervaccinated, and 8% were never vaccinated.
Of the 103 individuals (60.2%) aged 12 years, 85% were fully vaccinated,
7% were undervaccinated, and 8% were never vaccinated."
http://cid.oxfordjournals.org/content/54/12/1730.full
Effectiveness of pertussis vaccines for adolescents and adults: case-control

study
"The adjusted estimate of effectiveness of Tdap vaccination against pertussis
was 53.0."
http://www.bmj.com/content/347/bmj.f4249
"vaccination led to a 40-fold enhancement of B. parapertussis colonization in

the lungs of mice.. these data suggest that the vaccine may be contributing
to the observed rise in whooping cough incidence over the last decade by
promoting B. parapertussis infection.
http://www.cidd.psu.edu/research/synopses/acellular-vaccine-enhancementb.-parapertussis
Conclusions
"In low-income countries with high mortality, DTP as the last vaccine received
may be associated with slightly increased mortality. Since the pattern was
inversed for BCG, the effect is unlikely to be due to higher-risk children having
received vaccination. The role of DTP in high mortality areas needs to be
clarified."
The odds of having a history of asthma was twice as great among vaccinated
subjects than among unvaccinated subjects (adjusted odds ratio, 2.00; 95%
confidence interval, 0.59 to 6.74). The odds of having had any allergy-related
respiratory symptom in the past 12 months was 63% greater among
vaccinated subjects than unvaccinated subjects (adjusted odds ratio, 1.63;
95% confidence interval, 1.05 to 2.54). The associations between vaccination
and subsequent allergies and symptoms were greatest among children aged
5 through 10 years.
DTP or tetanus vaccination appears to increase the risk of allergies and
related respiratory symptoms in children and adolescents. Although it is
unlikely that these results are entirely because of any sources of bias, the
small number of unvaccinated subjects and the study design limit our ability
to make firm causal inferences about the true magnitude of effect.
***Vaccines in pregnancy***
(articles and studies)
A video of Dr. Blaylock explaining https://www.facebook.com/669084493234593/videos/701407633335612/

https://vactruth.com/2012/11/23/flu-shot-spikes-fetal-death/
http://journeyboost.com/2014/11/13/flu-shots-in-pregnancy-2/
http://www.vaccinationinformationnetwork.com/vaccinations-duringpregnancy-resource-page-2/
http://www.modernalternativepregnancy.com/2015/11/16/flu-vaccines-unsafeand-ineffective-for-pregnant-women/
Dr. Paul video warning for pregnant moms
https://m.youtube.com/watch?v=VoY6vXEMsU8
http://www.tandfonline.com/doi/abs/10.1080/02772248.2012.724574?
journalCode=gtec20#/doi/abs/10.1080/02772248.2012.724574?
journalCode=gtec20
Tdap
http://www.thehealthyhomeeconomist.com/tdap-vaccine-pushed-onpregnant-women-despite-fetal-risks/
https://m.youtube.com/watch?v=c3EEuMGhCwA
https://cogforlife.org/2009/12/20/pregnant-women-and-the-h1n1-vaccine/
http://articles.mercola.com/sites/articles/archive/2013/11/10/vaccinationduring-pregnancy.aspx
http://paulthomasmd.com/2015/11/09/should-i-get-the-tdap-while-pregnantdoes-my-newborn-need-the-hepatitis-b-vaccine/
***AUTISM***
"Boys vaccinated as neonates had threefold greater odds for autism

diagnosis compared to boys never vaccinated or vaccinated after the first
month of life. Non-Hispanic white boys were 64% less likely to have autism
diagnosis relative to nonwhite boys. Findings suggest that U.S. male neonates
vaccinated with the hepatitis B vaccine prior to 1999 (from vaccination
record) had a threefold higher risk for parental report of autism diagnosis
compared to boys not vaccinated as neonates during that same time period.
Nonwhite boys bore a greater risk."
Conclusions
The present study provides new epidemiologic evidence showing that African
American males receiving the MMR vaccine prior to 24 months of age or 36

months of age are more likely to receive an autism diagnosis.
http://web.archive.org/web/20140824230839/http://www.translationalneurode
generation.com/content/3/1/16/abstract
Hypothesis: conjugate vaccines may predispose children to autism spectrum

disorders.
"the potential effects of conjugate vaccines on neural development merit
close examination. Conjugate vaccines fundamentally change the manner in
which the immune systems of infants and young children function by
deviating their immune responses to the targeted carbohydrate antigens
from a state of hypo-responsiveness to a robust B2 B cell mediated response.
This period of hypo-responsiveness to carbohydrate antigens coincides with
the intense myelination process in infants and young children, and conjugate
vaccines may have disrupted evolutionary forces that favored early brain
development over the need to protect infants and young children from
capsular bacteria."
Serological association of measles virus and human herpesvirus-6 with brain

autoantibodies in autism.
"Considering an autoimmunity and autism connection, brain autoantibodies
to myelin basic protein (anti-MBP) and neuron-axon filament protein (antiNAFP) have been found in autistic children. In this current study, we
examined associations between virus serology and autoantibody by
simultaneous analysis of measles virus antibody (measles-IgG), human
herpesvirus-6 antibody (HHV-6-IgG), anti-MBP, and anti-NAFP. We found that
measles-IgG and HHV-6-IgG titers were moderately higher in autistic children
but they did not significantly differ from normal controls. Moreover, we found
that a vast majority of virus serology-positive autistic sera was also positive
for brain autoantibody: (i) 90% of measles-IgG-positive autistic sera was also
positive for anti-MBP; (ii) 73% of measles-IgG-positive autistic sera was also
positive for anti-NAFP; (iii) 84% of HHV-6-IgG-positive autistic sera was also
positive for anti-MBP; and (iv) 72% of HHV-6-IgG-positive autistic sera was
also positive for anti-NAFP. This study is the first to report an association
between virus serology and brain autoantibody in autism; it supports the
hypothesis that a virus-induced autoimmune response may play a causal role
in autism."
Abstract
"There is a compelling argument that the occurrence of regressive autism is
attributable to genetic and chromosomal abnormalities, arising from the
overuse of vaccines, which subsequently affects the stability and function of
the autonomic nervous system and physiological systems. That sense
perception is linked to the autonomic nervous system and the function of the
physiological systems enables us to examine the significance of autistic
symptoms from a systemic perspective. Failure of the excretory system
influences elimination of heavy metals and facilitates their accumulation and
subsequent manifestation as neurotoxins: the long-term consequences of
which would lead to neurodegeneration, cognitive and developmental
problems. It may also influence regulation of neural hyperthermia. This article
explores the issues and concludes that sensory dysfunction and systemic
failure, manifested as autism, is the inevitable consequence arising from
subtle DNA alteration and consequently from the overuse of vaccines."
Empirical Data Confirm Autism Symptoms Related to Aluminum and

Acetaminophen Exposure
Autism is a condition characterized by impaired cognitive and social skills,
associated with compromised immune function. The incidence is alarmingly
on the rise, and environmental factors are increasingly suspected to play a
role. This paper investigates word frequency patterns in the U.S. CDC Vaccine
Adverse Events Reporting System (VAERS) database. Our results provide
strong evidence supporting a link between autism and the aluminum in
vaccines. A literature review showing toxicity of aluminum in human
physiology offers further support. Mentions of autism in VAERS increased
steadily at the end of the last century, during a period when mercury was
being phased out, while aluminum adjuvant burden was being increased.
Using standard log-likelihood ratio techniques, we identify several signs and
symptoms that are significantly more prevalent in vaccine reports after 2000,
including cellulitis, seizure, depression, fatigue, pain and death, which are
also significantly associated with aluminum-containing vaccines. We propose
that children with the autism diagnosis are especially vulnerable to toxic
metals such as aluminum and mercury due to insufficient serum sulfate and
glutathione. A strong correlation between autism and the MMR (Measles,
Mumps, Rubella) vaccine is also observed, which may be partially explained
via an increased sensitivity to acetaminophen administered to control fever.

http://www.mdpi.com/1099-4300/14/11/2227
full text: http://groups.csail.mit.edu/sls/publications/2012/entropy-1402227.pdf
"Acetaminophen use after measles-mumps-rubella vaccination was

SIGNIFICANTLY associated with autistic disorder when considering children 5
years of age or less, after limiting cases to children with regression in
development and when considering only children who had post-vaccination
sequelae adjusting for age, gender, mothers ethnicity, and the presence of
illness concurrent with measles-mumps-rubella vaccination. Ibuprofen use
after measles-mumps-rubella vaccination was not associated with autistic
disorder. This preliminary study found that acetaminophen use after measlesmumps-rubella vaccination was associated with autistic disorder."
Neurologic Adverse Events Following Vaccination (Progress in Health Sciences

Vol. 2(1) 2012pp 129-141.)
Conclusions: Despite the assurances of the necessity and safety of
vaccinations, there are more and more questions and doubts, which both
physicians and parents are waiting to be clarified It seems that it would be
worthwhile to apply the precautionary principle the ethical principle (from
1988) according to which if there is a probable, although poorly known, risk of
adverse effects of new technology, it is better not to implement it rather than
risk uncertain but potentially very harmful consequences.
http://progress.umb.edu.pl/sites/progress.umb.edu.pl/files/129-141.pdf
Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in

children with autism.
Thus the MMR antibody in autistic sera detected measles HA protein, which
is unique to the measles subunit of the vaccine. Furthermore, over 90% of
MMR antibody-positive autistic sera were also positive for MBP
autoantibodies, suggesting a strong association between MMR and CNS
autoimmunity in autism. Stemming from this evidence, we suggest that an
inappropriate antibody response to MMR, specifically the measles component

thereof, might be related to pathogenesis of autism.
"A 1% increase in vaccination was associated with an additional 680 children
having AUT or SLI. Neither parental behavior nor access to care affected the
results, since vaccination proportions were not significantly related
(statistically) to any other disability or to the number of pediatricians in a U.S.
state. The results suggest that although mercury has been removed from
many vaccines, other culprits may link vaccines to autism. Further study into
the relationship between vaccines and autism is warranted
Autoimmunity to the central nervous system (CNS), especially to myelin

basic protein (MBP), may play a causal role in autism, a neurodevelopmental
disorder. Because many autistic children harbor elevated levels of measles
antibodies, we conducted a serological study of measles-mumps-rubella
(MMR) and MBP autoantibodies. Using serum samples of 125 autistic children
and 92 control children, antibodies were assayed by ELISA or immunoblotting
methods. ELISA analysis showed a significant increase in the level of MMR
antibodies in autistic children. Immunoblotting analysis revealed the presence
of an unusual MMR antibody in 75 of 125 (60%) autistic sera but not in
control sera. This antibody specifically detected a protein of 73-75 kD of MMR.
This protein band, as analyzed with monoclonal anti bodies, was
immunopositive for measles hemagglutinin (HA) protein but not for measles
nucleoprotein and rubella or mumps viral proteins. Thus the MMR antibody in
autistic sera detected measles HA protein, which is unique to the measles
subunit of the vaccine. Furthermore, over 90% of MMR antibody-positive
autistic sera were also positive for MBP autoantibodies, suggesting a strong
association between MMR and CNS autoimmunity in autism. Stemming from
this evidence, we suggest that an inappropriate antibody response to MMR,
specifically the measles component thereof, might be related to pathogenesis
of autism.
Virus-induced autoimmunity may play a causal role in autism. To examine

the etiologic link of viruses in this brain disorder, we conducted a serologic
study of measles virus, mumps virus, and rubella virus. Viral antibodies were
measured by enzyme-linked immunosorbent assay in the serum of autistic
children, normal children, and siblings of autistic children. The level of

measles antibody, but not mumps or rubella antibodies, was significantly
higher in autistic children as compared with normal children (P = 0.003) or
siblings of autistic children (P <or= 0. 0001). Furthermore, immunoblotting of
measles vaccine virus revealed that the antibody was directed against a
protein of approximately 74 kd molecular weight. The antibody to this antigen
was found in 83% of autistic children but not in normal children or siblings of
autistic children. Thus autistic children have a hyperimmune response to
measles virus, which in the absence of a wild type of measles infection might
be a sign of an abnormal immune reaction to the vaccine strain or virus
reactivation. http://www.ncbi.nlm.nih.gov/pubmed/12849883
Adverse Drug Reactions of Spontaneous Reports in Shanghai Pediatric

Population
Results:
"A male overrepresentation was observed regarding the total number of
reports. The most frequently reported group of drugs were vaccines
(42.15%). Skin rash and fever were the commonest symptoms reported in the
total pediatric dataset. The proportion of children that suffered from a serious
ADR was 2.16% and that for drug related deaths was 0.34%. And we found
that the multiple drug exposure experienced a high proportion of serious
ADRs compared with the single drug use ( = 15.99, P<0.0001). Sixty-five
percent of ADRs were for children less than 6 years of age. And more than
half of reports were from doctors."
" The 3848 reports included 4430 suspected ADRs, with an average of over
10 reports per day and 1.15 ADRs per child. There were 666 reports, which
cited more than one suspected drug. The total number of suspected drugs in
pediatric reports was 4619 with a mean number of 1.20 drugs per child."
ADRs by Vaccines and Non-vaccines:
"The single most common reaction was exanthema, followed by fever,
application site reaction and vomiting. Regarding assessment of drugs, the
most frequent reports were related to vaccine use (1622 reports, 42.15%).
When the non-vaccine related reports were discriminated by excluding
children that had been reported to have a suspected ADR of a vaccination,
the total number of children, whom an ADR had been related to, were then
reduced to 2649. Skin reactions were still most frequently reported. The most
commonly reported drugs among serious reports were antibacterials for
systemic use (32.82%), nervous system (17.56%) and vaccines (13.74%)."
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3933652/...
*******
Poul Thorsen, the man that conducted the study for the CDC claiming there is
no link between vaccines and autism, is on the most wanted fugitive list for
the Office of Inspector General for stealing over $1 million in grant money
from the CDC. Thorsen submitted fraudulent invoices on CDC letterhead to
medical facilities assisting in the research for reimbursement of work
allegedly covered by the grants. The invoices were addressed to Aarhaus
University and Sahlgrenska University Hospital. The fact that the invoices
were on CDC letterhead made it appear that CDC was requesting the money
from Aarhaus University and Sahlgrenska University Hospital although the
bank account listed on the invoices belonged to Thorsen.
https://oig.hhs.gov/fraud/fugitives/profiles.asp#thorsen
"Thorsen's 2003 Danish study reported a 20-fold increase in autism in

Denmark after that country banned mercury based preservatives in its
vaccines. His study concluded that mercury could therefore not be the culprit
behind the autism epidemic.
His study has long been criticized as fraudulent since it failed to disclose that
the increase was an artifact of new mandates requiring, for the first time, that
autism cases be reported on the national registry. This new law and the
opening of a clinic dedicated to autism treatment in Copenhagen accounted
for the sudden rise in reported cases rather than, as Thorsen seemed to
suggest, the removal of mercury from vaccines."
http://www.huffingtonpost.com/robert-f-kennedy-jr/central-figure-in-cdcvac_b_494303.html
Thorsen's partner Kreesten Madsen recently came under fierce criticism after
damning e-mails surfaced showing Madsen in cahoots with CDC officials
intent on fraudulently cherry picking facts to prove vaccine safety.
http://www.putchildrenfirst.org/chapter5.html
"Rising autistic disorder prevalence is directly related to vaccines

manufactured utilizing human fetal cells."
http://www.ms.academicjournals.org/article/article1409245960_Deisher%20et
%20al.pdf
30 Scientific studies that demonstrate vaccines can and do cause autism.

https://healthimpactnews.com/2013/30-scientific-studies-showing-the-linkbetween-vaccines-and-autism/
***********
**Wakefield and whistleblower information**

Read Dr. Thompson's whistleblower statement:
http://morganverkamp.com/statement-of-william-w-thompson-ph-d-regardingthe-2004-article-examining-the-possibility-of-a-relationship-between-mmrvaccine-and-autism/
The lies spread about Wakefield:

1. His work was a scientific "study"--NO
Wakefield et al actually published a "paper". Scientific papers are designed to
answer a simple question. In this case the question was; do children with
regressive autism have chronic enterocolitis?
http://www.thelancet.com/journals/lancet/article/PIIS01406736%2897%2911096-0/abstract
2. "His paper claimed the MMR caused autism"--NO

Wakefield et al's conclusions documented in his paper: "We identified
associated gastrointestinal (GI) disease and developmental regression in a
group of previously normal children, which was generally associated in time
with possible environmental triggers."
He does not say the MMR vaccine causes autism or even that the GI disease
was caused by the MMR. He answered the simple question that yes... GI
disease and developmental regression was seen in a group of "previously
normal children". Wakefield et al's conclusion is now validated with the
weight of scientific data. We now know that gastrointestinal disease is closely
related to autism; " microbiome-CNS signaling", "gut bacteria may contribute
to ASD", "overlaps with Crohn's disease, ulcerative colitis, and
autoimmunity", "microbiome growth", "Maladaptive behaviors correlate with
GI problems", "dietary factors may play a role as secondary triggers of
autism", "gastrointestinal dysfunction characterizes a subset of children with
ASD", "immune reactivity to gluten", "affected activity of brain regions",
"addressing GI problems", and on and on (science references).
http://autismrawdata.net/1/post/2013/12/dietary-therapies-gi-science.html
His paper's conclusions were REPLICATED and proven true:
Walker, S., Fortunato, J., Gonzalez, L., Krigsman, A. (2013). Identification of
unique gene expression profile in children with regressive autism spectrum
disorder (ASD) and ileocolitis. PlosOne. (Retrieved from
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0058058)
"Taken as a whole, the picture that emerges is one in which GI symptomatic
children with ASD in whom cellular infiltrate is present in the ileum and colon
have a distinct molecular signature that is consistent with the larger disease
categories of gastrointestinal disease, and more specifically, overlaps with
Crohn's disease, ulcerative colitis, and autoimmunity."
Krigsman et al. (2010). Clinical presentation and histologic findings at
ileocolonoscopy in children with autistic spectrum disorder and chronic
gastrointestinal sysmptoms. Libertas Academia. (Retrieved from
https://www.scribd.com/doc/211406298/Krigsman-Et-Al-2010)
Conclusions: Patients with autism or related disorders exhibiting chronic
gastrointestinal symptoms demonstrate ileal or colonic inflammation upon
light microscopic examination of biopsy tissue. Further work is needed to
determine whether resolution of histopathology with appropriate therapy is
accompanied by GI symptomatic and cognitive/behavioral improvement.
3. "Wakefield was charged with "fraud", or "forged data"--NO

The data in question was the pathology reports that showed gastointestinal
disease. Wakefield was not in charge of evaluating the pathology reports in
this paper that was the charge of Dr. John O' Leary an independent Dublin
pathologist. Dr. O'Leary stands by his reports, and they are not challenged by
the UK's General Medical Council (GMC).
The UK General Medical Council charged Wakefield with serious professional

misconduct and sanction, Wakefield was found guilty by the GMC (General
Medical Council, pg. 7 & 9).
Professor Walker-Smith was also charged with and found guilty of serious
professional misconduct and sanction, just as Wakefield. The description of
the charges were similar with one variation being the monies given to
Wakefield via the Legal Aid Board (LAB). On appeal all of the GMC's rulings
toward Walker-Smith were overturned. the UK High Court's Mr. Justice Mitting
criticized the U.K. General Medical Council, stating its judgment had been
"based on inadequate and superficial reasoning" (High Court Of Justice,
2010). The claims of the BMC were deemed false to which they did not appeal
this decision.
http://www.bailii.org/ew/cases/EWHC/Admin/2012/503.html
Professor Murch's official charges were also serious professional misconduct
and sanction. He was found guilty of professional misconduct but not of
sanction.
On 9 November, David Lewis of the National Whistleblower's Center in
Washington DC published a letter in the BMJ (http://bmj.com) arguing that
Wakefield did not commit research fraud.
http://www.bmj.com/rapid-response/2011/11/09/re-how-case-against-mmrvaccine-was-fixed
This comment typically refers to the clinical investigations carried out by
Walker-Smith, which included colonoscopies, barium studies, and lumbar
punctures (LP). On appeal this charge by the General Medical Council as
being "not clinically indicated" (pg. 4) was overturned by the U.K.'s High
Court Of Justice (High Court Of Justice, 2010).
It is also important to note that the children had a positive diagnosis of GI
disease through this workup, and were appropriately treated. The parents
gave full consent for the procedures and were satisfied with the diagnosis
and subsequent treatment. These children were not managed appropriately
by their general practitioners regarding their untreated colitis. Further the
LP's were ordered to asses the function of the CNS, which is appropriate since
we now know that autism is a brain (encephalopathy)/body disorder, and the
vaccine strain of measles has been found in the CNS of patients with
encephalitis (science references). Barium studies are routine in assessing the
upper GI tract.
******
**DNA and vaccines**

(aborted fetal cells)
Drugs and vaccines are too large to produce in a test tube, and therefore,
they must be manufactured using cell lines. The final products contain
contaminants from the cell line used to manufacture the drug or vaccine.
When primitive human cell lines (such as an aborted fetal cell line) are used,
these contaminants have the potential to trigger autoimmune diseases or
genomic instability. When we use aborted fetal produced vaccines or
cosmetics, we are also injecting or transferring DNA and viruses from the
aborted fetus used to create the cell line into our own bodies.
The contaminants found in vaccines and drugs that are manufactured using
aborted fetal cell lines present the perfect storm of contaminants to cause
genomic instability. Some childhood vaccines contain very high levels of short
human fetal DNA fragments, which gene therapy studies have taught us are
the perfect size to insert into our genes. Some childhood vaccines also
contain a retroviral contaminant called HERVK, which is in the same family of
retroviruses as the one that caused cancer in 4 of 9 boys.
http://soundchoice.org/research/hervk-references/
http://soundchoice.org/research/dna-fragments-research/
Vaccines that use aborted fetal cells in production:

Acambis 1000 (smallpox) Acambis -- MRC5
Avaxim (hepatitis A) Pateur Merieux -- MRC5
Biavax (mumps, rubella) Merck -- RA273, WI-38
Ervevax (rubella) Smithkilne Beecham -- MRC5
Havarix (hepatitis A) Smithkilne Beecham -- MRC5
Imovax HDCV, DCO (rabies) Pasteur Merieux Connaught -- MRC5

Meruvax II (rubella) Merck -- RA273, WI-38
MMR II (Measles, mumps, rubella) Merck Sharp & Dohme -- WI-38
MR VAX (measles, rubella) Merck -- RA273, WI-38
Poliovax (polio, IPV) MRC5
Priorix (measles, mumps, rubella) Smithkline Beecham -- MRC5
Proquad (mmr, chickenpox/varicella) Merck -- RA273, WI-38, MRC5
Twinrix (hepatitis A and B) GSK -- MRC5
VAQTA (hepatitis A) MSD -- MRC5
Varivax (chickenpox, varicella) MSD -- WI-38
Zostavax (shingles) Merck -- MRC5, WI-38
Product cost for aborted human fetal cells.

http://www.atcc.org/products/all/CCL-171.aspx.
http://www.atcc.org/products/all/CCL-75.aspx.
Thousands of studies used the wrong cells, and journals are doing nothing
https://www.statnews.com/2016/07/21/studies-wrong-cells/
Cell lines derived from Human Tumors for Vaccine Manufacture

http://www.fda.gov/.../VaccinesandRelatedBi.../UCM319573.pdf
Unfortunately, Dr. Deishers team discovered that the fetal DNA levels
ranged anywhere from 142ng 2000ng per dose, way beyond the so-called
safe level http://www.soundchoice.org/scpiJournalPubHealthEpidem0920..
Characteristics and viral propagation properties of a new human diploid cell

line, Walvax-2, cell substrate for vaccine production.
Epidemiologic and Molecular Relationship Between Vaccine Manufacture and

Autism Spectrum Disorder Prevalence.
Overview of measles and mumps vaccine: origin, present, and future of

vaccine production.
An inactivated hepatitis A viral vaccine of cell culture origin

Human Cell Strains in Vaccine Development

http://m.historyofvaccines.org/.../human-cell-strains...
Adventitious Agents and Vaccines - 3rd paragraph states, "In the past,
biologic products have served as vectors for viral diseases. Examples include
the contamination of yellow fever vaccine with hepatitis B virus in the 1940s
(because a human-derived excipient contained hepatitis B virus),
contamination of early polio and adenovirus vaccines with simian virus 40 (SV
40 cancer virus) in the late 1950s and early 1960s, contamination of blood
products with hepatitis viruses and HIV, and contamination of dura mater
grafts with the Creutzfeldt-Jakob (CJD) disease agent. In these examples,
either human or animal materials used in production usually caused the
contamination." http://wwwnc.cdc.gov/eid/article/7/7/01-7735_article
The argument that "the fetal tissues would just go to waste if they were not
used" was not accepted at the Nuremberg trials of scientists who used body
parts from concentration camp victims. This abuse of the child's body only
compounds the injustice of the original abortion, even if the vaccine

producers were in no way connected to the abortion.
http://www.hhs.gov/ohrp/archive/nurcode.html.
Cell Lines:
WI38- W=Wistar I=Institute 38= # of abortion used
tissue would be collected from the lungs of a female baby at 3 months
gestation
1964
The rubella virus clinically named RA273. R=Rubella, A=Abortus, 27=27th
fetus, 3=3rd tissue explant, which was then cultivated on the WI-38 aborted
fetal cell line. Stanley Plotkin would later reveal that 40 more babies were
aborted after RA273 was successfully isolated, with virus strains taken from
34 of them. A total of over 80 separate abortions were involved in the
research and final production of the present day rubella vaccine- 21 abortions
from the original WI-1 through WI-26 fetal cell lines that failed, plus WI-38
itself, plus 67 from the attempts to isolate the rubella virus.
https://explorevaccines.wordpress.com/.../fetal-cell.../.
Autism and Cancer Related to Human Fetal DNA in Vaccines. Study

http://www.globalresearch.ca/new-study-in-journal.../5402912
*********End DNA file*
***VACCINE INJURY AND COMPENSATION***
"This website features doctors from a variety of specialties who are speaking
publicly about the damage being done to babies, infants, children and adults.
Video is the preferred media so you can hear it directly from the doctors, in
their own words. There are also resources such as how to find a doctor in your
area who will respect your decision regarding vaccines and, if necessary, sign
your child's exemption form for school or daycare.
Your pediatrician will not warn you of the true risks of vaccination because
they don't want to scare you away from vaccinating, and regular office visits
for that purpose. They may actually believe that the "greater good" is being
served, even if your child is one of the many who are sacrificed under that
misguided rationalization. But, as you listen to each doctor here, you'll get a
few more pieces to the puzzle, and gradually, the big picture will emerge.
Based on that realization, you will have the information you need to make a
decision on whether to vaccinate, or to join the growing number of no-longervaccinating families who are reporting stunning good health in their
unvaccinated children, in comparison to their vaccinated siblings."
http://vaccine-injury.info
"This webpage provides information on how to file a vaccine injury claim,

links and resources on vaccine injury compensation to aid those who believe
that they have suffered a vaccine injury and to raise awareness of the
National Vaccine Injury Compensation Program.
NVIC's co-founders worked with Congress on the National Childhood Vaccine
Injury Act of 1986, which acknowledged that vaccine injuries and deaths are
real and that the vaccine injured and their families should be financially
supported and that vaccine safety protections were needed in the mass
vaccination system
The law preserved the right for vaccine injured persons to bring a lawsuit in
the court system if federal compensation is denied or is not sufficient. By
2010, the U.S. Court of Claims had awarded nearly $3 billion dollars to
vaccine victims for their catastrophic vaccine injuries, although two out of
three applicants have been denied compensation.
We invite you to use the links below to understand the law, injury claims
process and more."
http://www.nvic.org/injury-compensation.aspx
Compensation table:
http://www.hrsa.gov/vaccinecompensation/vaccinetable.html
Exactly how much has been paid out to families of vaccine injured and dead
children?
4,807 families have been paid for a total of $3,415,710,944.32.
http://www.hrsa.gov/vaccinecompensation/data/statisticsreport.pdf
NVIC reporting:
http://www.nvic.org/reportreaction.aspx
OR
Http://www.nvic.org/reporting-systems.aspx
" AAPS does not oppose vaccines. AAPS has never taken an anti-vaccine
position, although opponents have tried to paint that picture. AAPS has only
attempted to halt government or school districts from blanket vaccine
mandates that violate parental informed consent.
42 states have mandatory vaccine policies, and many children are required
22 shots by first grade.
According to government statistics, children under the age of 14 are three
times more likely to suffer adverse effects -- including death -- following the
hepatitis B vaccine than to catch the disease itself.
The Centers for Disease Control admits that the reported number of
adverse effects of vaccines is probably only 10% of actual adverse effects.
The Physician's Desk Reference cites adverse reactions to the hepatitis B in
less than 1 percent. However, if more than 70 million American children
receive the vaccine, that means more than 700,000 children are likely to
suffer adverse reactions.
Children are a very low risk group for hepatitis B. Primary risk factors are
dependent on lifestyle, i.e. multiple sex partners, drug abuse or an
occupation with exposure to blood.

Rampant conflicts of interest in the approval process has been the subject
of several Congressional hearings, and a recent Congressional report
concluded that the pharmaceutical industry has indeed exerted undue
influence on mandatory vaccine legislation toward its own financial interests.
The vaccine approval process has also been contaminated by flawed or
incomplete clinical trials, and government officials have chosen to ignore
negative results. For example, the CDC was forced to withdraw its
recommendation of the rotavirus vaccine within one year of approval. Yet
public documents obtained by AAPS show that the CDC was aware of
alarmingly high intussusception rates months before the vaccine was
approved and recommended.
Mandatory vaccines violate the medical ethic of informed consent. A case
could also be made that mandates for vaccines by school districts and
legislatures is the de facto practice of medicine without a license.
The CDC's own "Guide to Contraindications to Childhood Vaccination" warns
that when assessing children's common symptoms, "if any one of them is a
contraindication, DO NOT VACCINATE" [caps added]. And yet, under legislated
mandates, the vaccines are still required. "
http://www.aapsonline.org/testimony/mandvac.htm
"A recent study published in the Open Journal of Pediatrics (1) revealed the
stark truth that the mass media seems to refuse to acknowledge, the public is
in the dark about, and dissenting pediatricians wont reveal to their own
patients for fear of having their careers jeopardized or worse, their license to
practice medicine yanked.
A full 6% of pediatricians do not vaccinate their own children according to
CDC guidelines and a whopping 13% do not plan to follow CDC guidelines
when vaccinating their children in the future. When you expand the scenario
to include pediatric specialists, the number jumps to 21%.
With regard to the MMR vaccine, the numbers arent much better regarding
CDC compliance.
5% of general pediatricians and 19% of pediatric specialists planned to
postpone the MMR jab for their own children until after 18 months of age,
beyond CDC guidelines.
The most common reasons why pediatricians have already avoided at least
one vaccine for their children, or plan to avoid vaccines for future children,
are concerns about safety and too many vaccines given at once.
Sounds like exactly the same reasoning as uncredentialed Moms and Dads
who choose not to vaccinate their children!"
http://www.thehealthyhomeeconomist.com/13-percent-of-pediatricians-rejectcdc-vax-schedule-for-their-own-children/
***
***SIDS AND VACCINE INDUCED DEATHS***
Death Has Always Been A Vaccine Complication

From the first human vaccines developed two centuries ago, smallpox and
rabies vaccines, death has always been a complication of vaccination.1 2 In
1933, the whole cell pertussis vaccines ability to kill without warning was
first reported in the medical literature when two infants died within minutes
of a pertussis shot.3 In 1946, American doctors detailed the sudden deaths of
twins within 24 hours of their second diphtheria-pertussis shot.4 In 1986, the
U.S. Congress passed the National Childhood Vaccine Injury Act and has
awarded over $2 billion dollars in compensation for deaths and injuries
caused by vaccines.5
U.S. Infant Mortality Rate High
According to the most recent National Vital Statistics Report, more than
26,000 American babies born alive in 2009 died before their first birthday,
which gives the U.S. a very high infant mortality rate of 6 infant deaths per
1,000 live births.6 In 1960, America ranked 12th in infant mortality among all
nations of the world. In 2005, we had fallen to number 30. Today in America,
there are more premature babies than ever before and more full term babies
die before their first birthday than in most European countries.7
Some people argue that not every country calculates their infant mortality
statistics the same way, which artificially inflates the poor ranking for the
U.S.8 Even if adjustments would boost the U.S. ranking up several notches,
there can be no question that a nation, which spends more per capita on
healthcare 9 and legally requires their children to get more vaccines than any
other country, should have one of the best not one of the worst infant
mortality rates, especially for healthy babies born full term.
http://www.nvic.org/NVIC-Vaccine-News/May-2011/In-Memoriam--InfantDeaths---Vaccination.aspx
*ALSO refer back to the first article i posted from the Journal of American
Physicians and Surgeons: "Our study showed that infants who receive several vaccines concurrently, as
recommended by CDC, are significantly more likely to be hospitalized or die
when compared with infants who receive fewer vaccines simultaneously. It
also showed that reported adverse e ects were more likely to lead to
hospitalization or death in younger infants."
www.jpands.org/vol21no2/miller.pdf
"Prior to contemporary vaccination programs, Crib death was so infrequent

that it was not mentioned in infant mortality statistics. In the United States,
national immunization campaigns were initiated in the 1960s when several
new vaccines were introduced and actively recommended. For the first time
in history, most US infants were required to receive several doses of DPT,
polio, measles, mumps, and rubella vaccines.
Shortly thereafter, in 1969, medical certifiers presented a new medical term
sudden infant death syndrome. In 1973, the National Center for Health
Statistics added a new cause-of-death categoryfor SIDSto the ICD. SIDS is
defined as the sudden and unexpected death of an infant which remains
unexplained after a thorough investigation. Although there are no specific
symptoms associated with SIDS, an autopsy often reveals congestion and
edema of the lungs and inflammatory changes in the respiratory system.
By 1980, SIDS had become the leading cause of postneonatal mortality
(deaths of infants from 28 days to one year old) in the United States. In 1992,
to address the unacceptable SIDS rate, the American Academy of Pediatrics
initiated a Back to Sleep campaign, convincing parents to place their infants
supine, rather than prone, during sleep. From 1992 to 2001, the postneonatal
SIDS rate dropped by an average annual rate of 8.6%.
However, other causes of sudden unexpected infant death (SUID) increased.
For example, the postneonatal mortality rate from suffocation in bed

increased during this same period at an average annual rate of 11.2%. The
postneonatal mortality rate from suffocation-other, unknown and
unspecified causes', and due to intent unknown in the External Causes of
Injury section, all increased during this period as well. (In Australia, Mitchell et
al. observed that when the SIDS rate decreased, deaths attributed to
asphyxia increased. Overpeck et al. and others, reported similar
observations.)
A closer inspection of the more recent period from 1999 to 2001 reveals that
the US postneonatal SIDS rate continued to decline, but there was no
significant change in the total postneonatal mortality rate. During this period,
the number of deaths attributed to suffocation in bed and unknown causes,
increased significantly. According to Malloy and MacDorman, 'If death-certifier
preference has shifted such that previously classified SIDS deaths are now
classified as suffocation, the inclusion of these suffocation deaths and
unknown or unspecified deaths with SIDS deaths then accounts for about 90
percent of the decline in the SIDS rate observed between 1999 and 2001 and
results in a non-significant decline in SIDS'.
Although some studies were unable to find correlations between SIDS and
vaccines, there is some evidence that a subset of infants may be more
susceptible to SIDS shortly after being vaccinated. For example, Torch found
that two-thirds of babies who had died from SIDS had been vaccinated
against DPT (dip. htheriapertussistetanus toxoid) prior to death. Of these,
6.5% died within 12 hours of vaccination; 13% within 24 hours; 26% within 3
days; and 37%, 61%, and 70% within 1, 2, and 3 weeks, respectively. Torch
also found that unvaccinated babies who died of SIDS did so most often in the
fall or winter while vaccinated babies died most often at 2 and 4 monthsthe
same ages when initial doses of DPT were given to infants.
He concluded that DPT 'may be a generally unrecognized major cause of
sudden infant and early childhood death, and that the risks of immunization
may outweigh its potential benefits. A need for re-evaluation and possible
modification of current vaccination procedures is indicated by this study.'
Walker et al. found 'the SIDS mortality rate in the period zero to three days
following DPT to be 7.3 times that in the period beginning 30 days after
immunization.' Fine and Chen reported that babies died at a rate nearly eight
times greater than normal within 3 days after getting a DPT vaccination."
~ Neil Z. Miller and Gary S. Goldman
_______________________________________
"CDC and FDA researchers identify 749 deaths linked to the administration of
the Hib vaccine, 51% of which were sudden infant death linked to the
administration of Hib vaccine in a publication of a new study in the Journal of
Pediatrics.
"Adverse events following Haemophilus influenzae type b vaccines in the

Vaccine Adverse Event Reporting System, 1990-2013."
The CDC has boldly denied that there is any evidence supporting a causal link
between vaccines and infant death, despite the fact that their own webpage
on the topic acknowledges that "From 2 to 4 months old, babies begin their
primary course of vaccinations. This is also the peak age for sudden infant
death syndrome (SIDS)." Written off as coincidence, the CDC suggests that
stomach sleeping is the primary modifiable risk factor."
http://www.greenmedinfo.com/blog/cdcs-own-data-vaccine-infant-death-link
Viera Scheibner is a retired principal research scientist with a doctorate in

natural sciences. During her distinguished career, she has published three
books and 90 scientific papers in prestigious scientific journals. Since the mid80's, she has done extensive research into vaccines and vaccinations. Her
first research was in the area of Sudden Infant Death Syndrome (SIDS). She
wasn't even studying vaccinations, but she stumbled onto a relationship
between SIDS and vaccinations that lead to a very deep study into
vaccination literature in medical journals. In 1983, she published her book on
the results of her research Vaccination: The Medical Assault on the Immune
System. She often provides expert reports for court cases involving
immunizations and vaccine-damaged individuals throughout the world.
http://www.consumerhealth.org/articles/display.cfm?ID=19990705002005
Infant mortality rates regressed against number of vaccine doses routinely
given: Is there a biochemical or synergistic toxicity?

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170075/#bibr250960327111407644 Almost no SIDS prior to vaccine programs

http://www.ncbi.nlm.nih.gov/pubmed/18538957 SIDS and vaccines
and vaccines study
Infant mortality
vaccines
Both twins die after
vaccine
SIDS after hexavalent
Have you ever searched the Vaccine Adverse Events Reporting System
(VAERS)?
Go to this link: http://www.medalerts.org/vaersdb/index.php
Skip section 1.
Go to Section 2 where it says, "Select Symptoms." Look to the right and click
on the little white upside-down triangle to "open." Scroll down and click on
Sudden Infant Death Syndrome. You will see it transfer to the form on the
right, under "Currently Selected Symptoms."
Skip sections 3 & 4.
Go to Section 5 where it says, "Select Demographics."
Go to the box on the right, where it says "Age Range."
Click the round circle, then enter 0 in the "From" box and 1 in the "To" box.
Now look at the blue bar directly above the Age Range data fields and click
the little gray box that says "FIND."
Your search results will pop up in a new window.
1,228 cases where age is under 1 and symptom is Sudden Infant Death
Syndrome.
Now you can scroll down and read the death reports that have been made to
VAERS. Notice how many of them occurred within 24 hours of vaccinations.
Notice how many say the death was ruled SIDS.
And remember, the AMA reports that less than 10% of all reactions to any
medical product are ever reported, and that includes reactions to vaccines.
Doctors are mandated by the 1986 Childhood Vaccine Injury Law to report
vaccine-injuries.
There are no consequences to doctors for not reporting. Research conducted
by NVIC and others indicates that between 1-2% of all doctors EVER files a
report to VAERS.
The query I just walked you through only returned those deaths that were
assigned a "Sudden Infant Death" cause of death.
When you change the symptom to "ALL" (the default), and select "Died" in
Section 4: Event Characteristics, (leave the age range the same), there are
2,883 deaths that have been reported in children between birth and 1 year
---------------------------------
***VITAMIN K *VACCINE* INJECTION***
I get a lot of backlash for using the term vaccine when speaking about the
vitamin injection. I, myself have heard pediatricians, OBs and other medical
professional use that term when referring to it. It has the same adjuvants
used in vaccines. Vitamin K has 100 mcg of aluminum in one dose. The
aluminum in the vaccines, is a known neurotoxin and is proven to cause
immunological disorders, neurological disorders, and lifelong brain
inflammation.
Aluminum (Al), the most commonly used vaccine adjuvant, is a

demonstrated neurotoxin and a strong immune stimulator. Hence, adjuvant Al
has the potential to induce neuroimmune disorders. When assessing adjuvant

toxicity in children, two key points ought to be considered: (i) children should
not be viewed as "small adults" as their unique physiology makes them much
more vulnerable to toxic insults; and (ii) if exposure to Al from only few
vaccines can lead to cognitive impairment and autoimmunity in adults, is it
unreasonable to question whether the current pediatric schedules, often
containing 18 Al adjuvanted vaccines, are safe for children?
There is also a concerning scarcity of data on toxicology and

pharmacokinetics of these compounds. In spite of this, the notion that
aluminum in vaccines is safe appears to be widely accepted. Experimental
research, however, clearly shows that aluminum adjuvants have a potential
to induce serious immunological disorders in humans. In particular, aluminum
in adjuvant form carries a risk for autoimmunity, long-term brain
inflammation and associated neurological complications and may thus have
profound and widespread adverse health consequences.
Adverse reactions VitK

Severe hypersensitivity reactions, including anaphylactoid reactions and
deaths have been reported following parenteral administration. The majority
of these reported events occurred following intravenous administration (see
Box Warning.)
The possibility of allergic sensitivity, including an anaphylactoid reaction,
should be kept in mind following parenteral administration.
Transient "flushing sensations" and "peculiar" sensations of taste have been
observed, as well as rare instances of dizziness, rapid and weak pulse,
profuse sweating, brief hypotension, dyspnea, and cyanosis.
Pain, swelling, and tenderness at the injection site may occur.
Infrequently, usually after repeated injection, erythematous, indurated,
pruritic plaques have occurred; rarely, these have progressed to sclerodermalike lesions that have persisted for long periods. In other cases, these lesions
have resembled erythema perstans.
Hyperbilirubinemia has been observed in the newborn following
administration of phytonadione. This has occurred rarely and primarily with
doses above those recommended.
http://web.archive.org/web/20070213093306/http://www.fda.gov/medwatch/S
AFETY/2003/03Feb_PI/AquaMEPHYTON_PI.pdf
Studies have linked large doses of vitamin K with childhood cancers and
leukemia, this large dose of synthetic K administered within minutes of birth
seems questionable at best.
http://www.thehealthyhomeeconomist.com/skip-that-newborn-vitamin-k-shot/
Carcinogenesis, Mutagenesis, Impairment of Fertility

Studies of carcinogenicity, mutagenesis or impairment of fertility have not
been conducted with Vitamin K1 Injection (Phytonadione Injectable Emulsion,
USP).
https://www.drugs.com/pro/vitamin-k1.html
Not been studied?!?!
INGREDIENT LIST (I suggest that you google the MSDS for each of these to
find out exactly what they are and whether or not they're toxic to the human
body.)
Each milliliter contains
Phytonadione ........................... 2 mg or 10 mg
Inactive ingredients:
Polyoxyethylated fatty acid derivative ... 70 mg
Dextrose ............................................ 37.5 mg
Water for Injection, q.s. ........................... 1 mL
Added as preservative:Benzyl alcohol .... 0.9%

https://www.scribd.com/doc/33874512/Merck-Vitamin-K-Package-InsertAquamephyton-PI
WarningsBenzyl alcohol as a preservative in Bacteriostatic Sodium Chloride Injection

has been associated with toxicity in newborns. Data are unavailable on the
toxicity of other preservatives in this age group.
https://www.hospira.com/en/images/EN-0538_tcm81-5411.pdf
(Read that again ... it is known to be toxic to newborns, and the toxicity info is
unavailable ... because it has never been properly safety tested.)
Benzyl alcohol is believed to have a role in the increased frequency of

cerebral intraventricular hemorrhages and mortality reported in very-lowbirth-weight (VLBW) infants (weight < 1000 g) who received flush solutions
preserved with benzyl alcohol. An increased incidence of developmental
delay and cerebral palsy is also noted in the same VLBW patient population,
suggesting a secondary damaging effect of benzyl alcohol.
Click here to read the rest:
https://pubchem.ncbi.nlm.nih.gov/compound/benzyl_alcohol#section=DrugWarning
As early as April 17, 1977, an article in one of the world's most esteemed
medical journals, the Lancet, discredited the policy of routine vitamin K
injections. "We conclude that healthy babies, contrary to current beliefs, are
not likely to have a vitamin K deficiency... the administration of vitamin K is
not supported by our findings..." Van Doorm et al stated in the Lancet article.
VKR cited 21 peer-reviewed reports that had been published in prominent
medical journals. All of them concur that policies that mandate the universal
injection of newborn babies are not based on sound science. There has been
much peer-reviewed evidence generated which questions the efficacy of
routine vitamin K injections as sound public health policy.
http://www.vaccination.inoz.com/VitaminK.html
Here's the vitamin K1 (phytonadione) black box warning:

Black Box Warnings
Severe reactions, including fatalities, have occurred during and immediately
after IV administration, even when precautions have been taken with proper
dilution and avoidance of rapid infusion
Severe reactions also reported after IM administration; typically, these severe
reactions involve hypersensitivity or anaphylaxis and include shock and
cardiac or respiratory arrest
IV/IM reactions may occur with first dose (no prior exposure to phytonadione)
Restrict use of IV/IM routes to situations where SC administration is not
feasible and serious risk involved is considered justified
http://reference.medscape.com/drug/vitamin-k-mephyton-vitamin-k1phytonadione-344424#5
The patent applications are a terrifying read!

Patent US 20130189316 A1
"Since vitamin K is insoluble in water, a number of solubilization methods
have been tried to dissolve it for injection. PIE-USP is an aqueous solution
that contains polyoxyethylated fatty acid, which is a strong detergent (also
known as Cremophor), to solubilize vitamin K.
The injection of a high HLB surfactant or detergent such as Cremophor,

polysorbate 80 or HCO-60 can cause hypersensitivity reactions or, more
severely, anaphylaxis. The potential for such sometimes fatal reactions is well
documented for all Cremophor-containing drugs."
http://www.google.com/patents/US20130189316
Patent US 5021570 A
(Do you have nut, soy or egg sensitivities or allergies?)
"Preferable examples of the hydrogenated lecithin to be used in the present
invention are hydrogenated soybean and yolk lecithins. This hydrogenated

lecithin preferably comprises at least 85% of phospholipids and at least 60%,
based on the phospholipids, of phosphatidylcholine and has an iodine number
of 10 to 60, still preferably 25 to 50 (cf. Japanese Patent Laid-Open No.
62010/1980). The aqueous solution of the present invention preferably
contains 0.05 to 3% by weight of the hydrogenated lecithin.
Examples of the vegetable oils to be used in the present invention include

soybean, sesame, olive, cottonseed, tsubaki, rapeseed, peanut and corn oils."
http://www.google.com/patents/US5021570?dq=peanut%20%22vitamin%20K
%22
******* HERD IMMUNITY FROM VACCINES IS SCIENTIFICALLY IMPOSSIBLE****

http://sanevax.org/vaccines-and-the-myth-of-herd-immunity/
http://www.polkmoms.com/forum/topics/herd-immunty-from-vaccines-isnothing-more-than-vaccine-quotas
http://www.h4cblog.com/vaccines-and-the-myth-of-herd-immunity
http://www.heraldscotland.com/opinion/13047873.Mumps_vaccination_progra
mme_jeopardises_male_fertility_rates/
http://vaccinechoicecanada.com/about-vaccines/general-issues/herdimmunity/herd-immunity-the-misplaced-driver-of-universal-vaccination/
http://www.vacfacts.info/the-false-theory-of-vaccine-derived---herdimmunity.html
http://www.naturalnews.com/035024_vaccine_exemptions_children_infectious
_disease.html
http://www.vaccineriskawareness.com/The-Herd-Immunity-Theory-TreatingOur-Children-Like-Cattle
http://www.vaccinationcouncil.org/2012/07/05/herd-immunity-the-flawedscience-and-failures-of-mass-vaccination-suzanne-humphries-md-3/
https://thepeopleschemist.com/reasons-dont-vaccinate-children-vaccinesupporters-shouldnt-give/
http://www.thehealthyhomeeconomist.com/if-you-are-in-support-ofvaccinations/
http://vactruth.com/2010/01/31/forced-vaccinations-government-and-thepublic-interest/
http://www.wellwithin1.com/herdimmunity.htm (many links)
http://www.thehealthyhomeeconomist.com/the-herd-immunity-myth-andhow-it-pits-parent-against-parent/
http://vaxtruth.org/2012/05/measles-mumps-and-zombies-oh-my/
http://www.whale.to/a/herd.html
http://naturalsociety.com/exposing-vaccination-for-immunity-fraud/
http://www.sott.net/article/252159-The-entire-vaccine-industry-is-beingexposed-for-unproven-assumptions-and-misrepresentations-of-data
https://nyinjeksjon.wordpress.com/2012/03/02/kan-man-stille-sporsmalvedrorende-vaksinering-mot-meslinger/ (Norwegian)
http://www.rolfkenneth.no/Vax-E_Flokkimmunitet.html (Norwegian)
https://www.facebook.com/media/set/?
set=a.10150170317093998.359926.69667273997&type=1
http://www.greenmedinfo.com/blog/bioethicist-parents-should-be-held-liabeldeaths-caused-unvaccinated-children?
utm_source=www.GreenMedInfo.com&utm_campaign=d4a7f2513aGreenmedinfo&utm_medium=email&utm_term=0_193c8492fb-d4a7f2513a86916601
http://healthimpactnews.com/2013/herd-immunity-three-reasons-why-i-dontvaccinate-my-children-and-why-vaccine-supporters-shouldnt-care/
http://www.cancertruth.net/2013-septembernewsletter/#sthash.FMd5AGl7.dpbs
http://www.naturalnews.com/048770_MMR_vaccine_measles_immune_damag
e.html#ixzz3StGyBHh7
http://vaccineimpact.com/2013/mmr-vaccinations-abject-failure-in-measlesand-mumps/
http://business.financialpost.com/fp-comment/junk-science-weekvaccinating-the-herd
http://www.vaccinationcouncil.org/2012/02/18/the-deadly-impossibility-ofherd-immunity-through-vaccination-by-dr-russell-blaylock/
http://www.greenmedinfo.com/blog/herd-immunity-myth-or-reality
http://sanevax.org/herd-immunity-fact-or-fiction/
https://leviquackenboss.wordpress.com/2015/02/23/20-things-i-wish-vaccinejunkies-would-admit/
http://www.naturalnews.com/048770_MMR_vaccine_measles_immune_damag
e.html#ixzz3StGyBHh7
http://blog.realhealthtalk.com/heard-of-herd-immunity/
http://www.jeremyrhammond.com/2015/07/05/a-measles-death-vaccinesand-the-medias-failure-to-inform/
http://articles.mercola.com/sites/articles/archive/2009/11/14/expertpediatrician-exposes-vaccine-myths.aspx
https://jonrappoport.wordpress.com/2014/11/13/vaccines-and-herdimmunity-nonsense/
http://sanevax.org/wp-content/uploads/2015/05/Herd-Immunity-.pdf
http://edgytruth.com/2015/09/17/the-truth-cant-be-hidden-much-longer/?
utm_source=CCNewsletter&utm_medium=Email&utm_campaign=TheTruthAb
outVaccines
http://voiceforvaccinerealism.blogspot.co.uk/2015/05/what-aboutherd_17.html?m=1
https://thereisnoherdimmunity.wordpress.com/2016/02/01/vaccine-inducedherd-immunity-is-scientifically-impossible/
***MORE STUDIES I HAVENT HAD TIME TO GO THROUGH AND GET INSERTED

TEXT YET***
*********************************************************************
Vaccines: comprehensive list of resources, studies, scientific articles,

documentaries, vaccine friendly doctors, reasons others have to not
vaccinate.
Lots of good info out there. This isn't even the half of it. The list of trusted
resources/documentaries/doctors:
1. Dr. Nancy Banks - http://bit.ly/1Ip0aIm

2. Dr. Russell Blaylock - http://bit.ly/1BXxQZL
3. Dr. Shiv Chopra - http://bit.ly/1gdgh1s
4. Dr. Sherri Tenpenny - http://bit.ly/1MPVbjx
5. Dr. Suzanne Humphries - http://bit.ly/17sKDbf
6. Dr. Larry Palevsky - http://bit.ly/1LLEjf6
7. Dr. Toni Bark - http://bit.ly/1CYM9RB
8. Dr. Andrew Wakefield - http://bit.ly/1MuyNzo
9. Dr. Meryl Nass - http://bit.ly/1DGzJsc
10. Dr. Raymond Obomsawin - http://bit.ly/1G9ZXYl
11. Dr. Ghislaine Lanctot - http://bit.ly/1MrVeUL
12. Dr. Robert Rowen - http://bit.ly/1SIELeF
13. Dr. David Ayoub - http://bit.ly/1SIELve
14. Dr. Boyd Haley PhD - http://bit.ly/1KsdVby
15. Dr. Rashid Buttar - http://bit.ly/1gWOkL6
16. Dr. Roby Mitchell - http://bit.ly/1gdgEZU
17. Dr. Ken Stoller - http://bit.ly/1MPVqLI
18. Dr. Mayer Eisenstein - http://bit.ly/1LLEqHH
19. Dr. Frank Engley, PhD - http://bit.ly/1OHbLDI

20. Dr. David Davis - http://bit.ly/1gdgJwo
21. Dr Tetyana Obukhanych - http://bit.ly/16Z7k6J
22. Dr. Harold E Buttram - http://bit.ly/1Kru6Df
23. Dr. Kelly Brogan - http://bit.ly/1D31pfQ
24. Dr. RC Tent - http://bit.ly/1MPVwmu
25. Dr. Rebecca Carley - http://bit.ly/K49F4d
26. Dr. Andrew Moulden - http://bit.ly/1fwzKJu
27. Dr. Jack Wolfson - http://bit.ly/1wtPHRA
28. Dr. Michael Elice - http://bit.ly/1KsdpKA
29. Dr. Terry Wahls - http://bit.ly/1gWOBhd
30. Dr. Stephanie Seneff - http://bit.ly/1OtWxAY
31. Dr. Paul Thomas - http://bit.ly/1DpeXPf
32. Many doctors talking at once - http://bit.ly/1MPVHOv
33. Dr. Richard Moskowitz - http://bit.ly/1OtWG7D
34. Dr. Jane Orient - http://bit.ly/1MXX7pb
35. Dr. Richard Deth - http://bit.ly/1GQDL10
36. Dr. Lucija Tomljenovic - http://bit.ly/1eqiPr5
37. Dr Chris Shaw - http://bit.ly/1IlGiBp
38. Dr. Susan McCreadie - http://bit.ly/1CqqN83
39. Dr. Mary Ann Block - http://bit.ly/1OHcyUX
40. Dr. David Brownstein - http://bit.ly/1EaHl9A
41. Dr. Jayne Donegan - http://bit.ly/1wOk4Zz
42. Dr. Troy Ross - http://bit.ly/1IlGlNH
43. Dr. Philip Incao - http://bit.ly/1ghE7sS
44. Dr. Joseph Mercola - http://bit.ly/18dE38I
45. Dr. Jeff Bradstreet - http://bit.ly/1MaX0cC

46. Dr. Robert Mendelson - http://bit.ly/1JpAEQr
47. Dr. Garth Nicolson - http://bit.ly/1OQVJsF
48. Dr. Marc Girard - http://bit.ly/1iw0smT
49. Dr. Charles Richet - http://bit.ly/1G5GG7j
50. Dr. Zac Bush - http://bit.ly/1LS19OZ
DOCUMENTARIES
1. Vaccination - The Silent Epidemic - http://bit.ly/1vvQJ2W
2. The Greater Good - http://bit.ly/1icxh8j
3. Shots In The Dark - http://bit.ly/1ObtC8h
4. Vaccination The Hidden Truth - http://bit.ly/KEYDUh
5. Vaccine Nation - http://bit.ly/1iKNvpU
6. Vaccination - The Truth About Vaccines -http://bit.ly/1vlpwvU
7. Lethal Injection - http://bit.ly/1URN7BJ
8. Bought - http://bit.ly/1M7YSlr
9. Deadly Immunity - http://bit.ly/1KUg64Z
10. Autism - Made in the USA - http://bit.ly/1J8WQN5
11. Beyond Treason - http://bit.ly/1B7kmvt
12. Trace Amounts - http://bit.ly/1vAH3Hv
13. Why We Don't Vaccinate - http://bit.ly/1KbXhuf
14. Autism Yesterday - http://bit.ly/1URU2A7
Websites with lists of vaccine friendly doctors:

http://naturallynicole.com/naturally-nicoles-complete-list/
http://www.askdrsears.com//find-vaccine-friendly-doctor-ne
https://vactruth.com/2016/06/21/how-to-find-a-physician/
However once you decide you don't want vaccines, you also may also
discover you won't want much else peds have to offer - meds, meds and
more meds.
Many have switched to Naturopaths, Homeopaths, Holistic MD's, or
Chiropractors
Sometimes Osteopaths are more open; and sometimes Family Practice
Doctors
American Association of Naturopathic Physicians

206-298-0126
Referral number: 206-298-0125
www.naturopathic.org
American Holistic Medical Association

703-556-9245
www.holisticmedicine.org
American Naturopathic Medical Association

702-897-7053
http://anma.net
Holistic Pediatric Association

707-237-5312
http://www.hpakids.org
http://www.novaxdoctors.webs.com/
Functional medicine doctors are often less likely to push vaccines.

https://www.functionalmedicine.org/practitioner_search...
Another source is the International Chiropractic Pediatric Association:

http://www.icpa4kids.org/locator/index.php
If you're not sure about chiropractic and how it may help your child,
you can find answers here:
http://www.icpa4kids.org/why.htm
http://groups.yahoo.com/group/AP_Doctor_Referral/
http://www.mothering.com/discussions/
click on finding your tribe
Holistic Moms Network

http://www.holisticmoms.org/
click on "chapters' in the column on the right of the page
AANP - American Association of Naturopathic Physicians: Natural
NATUROPATHIC.ORG
Parent info:
http://thevoiceforchoice.com/informational-links/
Why are so many people choosing not to vaccinate?

http://www.greatmothersquestioningvaccines.com
http://vaxtruth.org/
http://thinktwice.com/
http://www.learntherisk.org/
https://vactruth.com/2014/12/12/10-reasons-not-to-vaccinate/
http://www.fhfn.org/50-reasons-not-to-vaccinate-your-children/
Attorney Demolishes Pro-Vaccine Talking Points, Lays Bare The Shocking Facts
About Vaccination Risks And Dangers
http://stateofthenation2012.com/?p=12072
CDCs own data proving that the MMR vaccine is deadlier than the measles,
mumps and rubella illnesses combined.
https://healthimpactnews.com/2015/zero-u-s-measles-deaths-in-10-years-butover-100-measles-vaccine-deaths-reported/
More pages with Scientific studies http://www.thinktwice.com/studies.htm

http://www.greatergoodmovie.org/learn-more/science/
http://vaccinepapers.org/scientific-papers-library/
http://www.learntherisk.org/studies/
http://thevoiceforchoice.com/adjuvents-preservatives/
http://www.dinnerforthought.com/vaccine-awareness/an-expansive-collectionof-vaccine-research
http://www.anh-usa.org/vaccine-science-is-not-settled-a-critical-review-of-theliterature/

Amy W&#39;s Final Vaccine Document

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Amy W&#39;s Final Vaccine Document

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It is an often a repeated fallacy that there is no research that supports the

These findings are so troubling that we expected major media outlets in

This is a file of 1000 peer reviewed scientific studies.

124 medical research on vaccine and autism

"There is no Federal requirement for informed consent relating to

All vaccine inserts in their entirety.

Aluminum (Al), the most commonly used vaccine adjuvant, is a

Aluminum is an experimentally demonstrated neurotoxin and the most

"In adults, aluminum exposure can lead to apparently age-related

adults; (iii) it is often assumed that peripheral immune responses do not

"Anxiety-like behavior was more pronounced among mice immunized with

Aluminum hydroxide (which is in vaccines) injections lead to motor deficits

"Aluminum-treated groups also showed significant motor neuron loss (35%)

the combination of adjuvants."

How aluminum, an intracellular ROS generator promotes hepatic and

"Repeated immunization with antigen causes systemic autoimmunity in mice

revision but not by cross-reaction to immunizing antigen, and subsequently

Autoimmunity and non-accidental injury in children

vaccination and hyperglycaemia implies hypoinsulinism, an autoimmune

" Encephalitis can occur in the following ways:

The common immunogenic etiology of chronic fatigue syndrome: from

Review of Vaccine Induced Immune Overload and the Resulting Epidemics of

system reacting to the immune overload. The epidemic of

Effectiveness of trivalent inactivated influenza vaccine in influenza-related

" A majority of the ophthalmological complications seen following hepatitis B

"Acquired autoimmunity syndromes occur after viral vaccinations. Molecular

Waning of Maternal Antibodies Against Measles, Mumps, Rubella, and

"Conclusions: Children of mothers vaccinated against measles and, possibly,

Limited and localized outbreak of newly emergent type 2 vaccine-derived

Breast milk makes rotavirus vaccine less effective

"We examined fecal shedding of pentavalent rotavirus vaccine (RV5) for 9

" Vaccine-type rotavirus was detected in all 50 antigen-positive specimens

These vaccines contain either trace or significant amounts of

INGESTION VS INJECTION- Mercury

early postnatal administration of thimerosal (four i.m. injections, 12 or 240 g

Maternal transfer of mercury to the developing embryo/fetus: is there a safe

Unvaccinated children do not significantly contribute to whooping cough

Effectiveness of pertussis vaccines for adolescents and adults: case-control

"vaccination led to a 40-fold enhancement of B. parapertussis colonization in

A video of Dr. Blaylock explaining https://www.facebook.com/669084493234593/videos/701407633335612/

"Boys vaccinated as neonates had threefold greater odds for autism

American males receiving the MMR vaccine prior to 24 months of age or 36

Hypothesis: conjugate vaccines may predispose children to autism spectrum

Serological association of measles virus and human herpesvirus-6 with brain

Empirical Data Confirm Autism Symptoms Related to Aluminum and

via an increased sensitivity to acetaminophen administered to control fever.

"Acetaminophen use after measles-mumps-rubella vaccination was

Neurologic Adverse Events Following Vaccination (Progress in Health Sciences

Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in

inappropriate antibody response to MMR, specifically the measles component

Autoimmunity to the central nervous system (CNS), especially to myelin

Virus-induced autoimmunity may play a causal role in autism. To examine

children, normal children, and siblings of autistic children. The level of

Adverse Drug Reactions of Spontaneous Reports in Shanghai Pediatric

"Thorsen's 2003 Danish study reported a 20-fold increase in autism in

"Rising autistic disorder prevalence is directly related to vaccines

30 Scientific studies that demonstrate vaccines can and do cause autism.

**Wakefield and whistleblower information**

The lies spread about Wakefield:

2. "His paper claimed the MMR caused autism"--NO

3. "Wakefield was charged with "fraud", or "forged data"--NO

The UK General Medical Council charged Wakefield with serious professional

**DNA and vaccines**

Vaccines that use aborted fetal cells in production:

Amy W's Final Vaccine Document

Amy W's Final Vaccine Document

Wakefield and whistleblower information

DNA and vaccines

VACCINE INJURY AND COMPENSATION

SIDS AND VACCINE INDUCED DEATHS

***VITAMIN K VACCINE INJECTION***

*** HERD IMMUNITY FROM VACCINES IS SCIENTIFICALLY IMPOSSIBLE