vaccines exposed

CONCLUSION OBJECTIONS ANSWERED
Today about 1 in 6 American children su ers from a What about the studies showing vaccines do
neurodevelopmental disorder, a large increase not cause autism?
compared to decades ago. Vaccines are very likely They look only at MMR, which does not contain Al and is
given at older ages when the brain is less sensitive to immune
contributing to this new health crisis. activation. Also, MMR-autism studies ignore reverse causality
bias, created when parents do not give MMR to children with
Vaccine advocates are silent about the research neurological damage caused by prior vaccines [11].
on Al adjuvant toxicity and immune activation. But aluminum has been used in vaccines for

There has never been a study of the entire over 80 years.
TRUE. But it has not been studied for safety until recently. Al
vaccine schedule, comparing health outcomes with dosage from vaccines increased dramatically in the last 25 years,
the unvaccinated. Further, vaccine studies almost in parallel with childhood neurodevelopmental disorders.
never use unvaccinated controls, but rather use other Aluminum is everywhere and ingested constantly.
vaccines or Al adjuvant as false placebos. Such It cannot be harmful.
research is unscienti c and cannot establish safety. 99.7% of ingested aluminum is not absorbed. The absorbed
0.3% comprises dissolved ions, which are rapidly eliminated in
A 1986 federal law completely protects vaccine urine. Al adjuvant comprises low-solubility Al nanoparticles, The most Powerful
manufacturers from all product liability lawsuits. which cannot be eliminated in urine and are far more harmful
than soluble Al.
Consequently, the industry has no incentive But immune activation studies are based on important scienti c evidence
to make safe vaccines. Perverse incentives resulting prenatal immune activation, not postnatal.
from this law encourage continued production of Most, but not all, immune activation studies use prenatal science is shows 2 ways
unsafe vaccines. exposure [8]. For years after birth the human brain remains
sensitive to immune activation. Consequently, postnatal being vaccines cause
Discuss this brochure at vaccinepapers.org/brochure. immune activation can damage the brain, just like prenatal
can. Also, the CDC recklessly promotes multiple vaccines for ignored.
pregnant women, causing prenatal exposure. brain damage.
Are there ways to prevent damage from aluminum
“...the existing evidence on the toxicology and pharma- and immune activation?
cokinetics of Al adjuvants…strongly implicate these YES. The nutrient silica removes Al from the body. Taurine
and curcumin reduce Al neurotoxicity [5]. Vitamin D regulates
compounds as contributors to the rising prevalence the e ect of immune activation, and has been observed to
1
of neurobehavioral disorders in children.” [3] reverse autism [12]. Aluminum Adjuvant Toxicity
— Dr C.A. Shaw (University of British Columbia) et al.
REFERENCES
“And what does a vaccination do? It activates the 1 Petrik et al. 2007 “Aluminum Adjuvant Linked to Gulf War Illness Induces Vaccines contain neurotoxic amounts of
immune system. That’s the point of vaccination... 2 Motor Neuron Death in Mice”, NeuroMolecular Medicine 9. PMID:17114826 aluminum, which can cause brain damage.
Shaw et al. 2009 “Aluminum Hydroxide Injections Lead to Motor De cits and
I think that universal vaccination of pregnant women 3 Motor Neuron Degeneration”, J. Inorg. Biochem. PMID:19740540.
2
Shaw et al. 2013 “Administration of aluminum to neonatal mice in vaccine-
could get us into a whole new set of problems.” (2006) relevant amounts is associated with adverse long term neurological outcomes”, Immune System Activation
— Dr Paul Patterson (California Institute of Technology) 4 J. Inorg. Biochem. PMID: 2393273 A developing brain can be damaged when
Khan et al. 2013 “Slow CCL2-dependent translocation of biopersistent particles
from muscle to brain”, BMC Medicine 11. PMID: 23557144
“Maternal immune activation yields male o spring 5 Sethi et al. 2009 “Curcumin Attenuates Aluminum-Induced Functional the immune system is activated by a vaccine.
Neurotoxicity in Rats”, Pharmacol Biochem Behav. 93. PMID: 19376155
with deficient social and communicative behavior, 6 Bilkei-Gorzo 1993 “Neurotoxic E ect of Enteral Aluminum”, Food Chem Toxicol. 31. Immune activation has been researched
PMID: 8505021
as well as high levels of repetitive behaviors, all of 7 Kneusel et al. 2014 “Maternal Immune Activation and Abnormal Brain extensively and is proven to cause autism
Development Across CNS Disorders”, Nature Reviews:Neurology, 10. PMID: 25311587

which are hallmarks of autism.” [9] 8 Wei et al. 2012 “Brain IL-6 Elevation Causes Neuroncal Circuitry Imbalances and and other brain damage.
Mediates Autism-Like Behaviors”, Biochim Biophys Acta. PMID: 22326556
— Dr Paul Patterson (California Institute of Technology) et al. 9 Malkova et al. 2012 “Maternal Immune Activation Yields O spring Displaying
Mouse Versions of the Three Core Symptoms of Autism”, Brain Behav Immun.
26. PMID 22310922
“Interleukin-6 is necessary and sufficient for produc- 10 Pineda et al. 2013 “Maternal Immune Activation Promotes Hippocampal
ing autism in the o spring… ” [10] 11 Kindling Epileptogenesis in Mice”, Ann Neurol. 74. PMID: 23907982
See VaccinePapers.org ~ Jain et al. review
— Dr Eduardo Pineda (David Ge en School of Medicine, UCLA) et al. 12 Jia et al. 2015 “Core Symptoms of Autism Improved After Vitamin D VaccinePapers.org
Supplementation”, Pediatrics 135. PMID: 25511123

Aluminum Adjuvant VaccinePapers.org CMSRI.org Immune Activation
FOR FURTHER READING:


Aluminum (Al) adjuvant is a vaccine ingredient used for Dosage of 550mcg/kg also caused excessive weight gain (a In early life, the brain and immune system develop together.
stimulating the immune system. It is used in many vaccines. sign of metabolic disorder). All 3 dosages (100, 300 and Communication chemicals (“cytokines”) used by the immune
Infants in the USA receive dosages of Al adjuvant that cause 550mcg/kg) also caused numerous signs of nerve damage system also guide brain development. Immune activation
brain damage in animal experiments. The dosages of Al (observable by microscopy and biochemical changes) and/or causes surges in cytokine production; cytokine surges during
adjuvant received according to the CDC vaccine schedule are:* abnormal anxious behavior. brain development cause permanent brain damage and
CDC VACCINE SCHEDULE All these results together are conclusive evidence of brain mental illnesses. The brain-damaging e ects of immune
Aluminum damage caused by the same dosages (mcg/kg) human infants activation have been studied extensively. The science is high
quality and there is a lot of it [7]. It is well-known that
Birth 147 mcg/kg (1 vaccine with 500 mcg, 3.4 kg infant) receive according to the US vaccine schedule. vaccines cause immune activation and can cause surges of
2 months 295 mcg/kg (6 vaccines with 1475 mcg, 5 kg infant) Vaccine advocates argue that injected Al adjuvant many di erent cytokines.
4 months 118 mcg/kg (5 vaccines with 772 mcg, 6.5 kg infant) is safe, based on studies of ingested Al salts. This is unscienti c Research has identi ed interleukin-6 (IL-6) as the speci c
6 months 184 mcg/kg (7 vaccines with 1475 mcg, 8 kg infant) because ingesting Al salts and injecting Al nanoparticles cytokine responsible for autism; IL-6 is stimulated by
present very di erent risks. Both the route of administration vaccine adverse reactions (fever, seizures). IL-6 causes all
TOTAL 744mcg/kg 19 vaccines and the chemical forms are di erent. three autism traits (social impairment, speech impairment
In scienti c experiments, dosages of 100mcg/kg, 300mcg/kg, Recent experiments prove that Al adjuvant is transported into and compulsive behavior), and damage to speci c brain
and 550mcg/kg Al adjuvant cause neuron death, muscle the brain by white blood cells [4]. This explains why injected structures (e.g., the cerebellum) known to be damaged in
weakness, learning and memory impairment, and pathological Al adjuvant can be more dangerous to the brain than ingested human autism. Both prenatal and postnatal surges of IL-6
behavior changes in animals. Al salts. can cause autism [8, 9].
Vaccine advocates like Paul O t make false statements about Immune activation during brain development has also been
*Aluminum dosage varies by vaccine manufacturer and infant weight. Al toxicity studies. The studies show that ingested Al is harmful at shown to cause schizophrenia, seizure disorders [10], and
Chart shows maximum possible dosages for average-weight infants. dosages less than half of what advocates claim to be safe [5, 6]. ADHD.
Charts and graphs below redrawn from originals
Motor Neuron Death 100mcg/kg Learning & Memory Impairment 300mcg/kg Social Behavior Impairment


1.0 30
100mcg/kg Control 300mcg/kg Immune activation
P<0.05 25
0.8 Al adjuvant 50 Al Adjuvant Al adjuvant caused mice to
Motor Neuron destroyed Maze impaired learning Preference 20 associate with
Population 0.6 about 35% of Completion and memory in for Social inanimate objects
(normalized) 0.4 motor neurons 25 mice. Impairment Interaction 15 instead of other
in mice in the Time is signi cant with (arb. units) 10 P<0.005 mice [6].
0.2 lower (lumbar) (seconds) P=0.0389 [2].
spine [1]. 5
0.0 0 0 1 2 3 4 0.0
Saline Control Al Adjuvant Saline Control Immune activation
Day
Muscle Strength Reduction 100mcg/kg Movement Impairment 550mcg/kg Compulsive Behavior Increase

Control 100mcg/kg 9 Control 550mcg/kg Al P<0.001
Al Adjuvant Al adjuvant Al Adjuvant adjuvant caused a 80
reduced 8 50% reduction in Immune activation
50 neuromuscular 7 walking speed (a 60 caused high levels of
Hang strength, as Walking 6 sign of neurological Buried repetitive/compulsive
Duration measured by Speed 5 damage) in Marbles behavior in mice
(seconds) 25 P<0.01 the duration (cm/sec) 4 male mice. Many (%) 40 (marble burying in
mice can 3 P<0.0001 other adverse this experiment) [6].
hang on a changes were also 20
0 wire mesh [1]. 2 observed. Al
0 5 10 15 20 25 1 adjuvant injected 0
Age (Weeks) 16 18 20 22 at ages 0-3 weeks Saline Control Immune activation
Aluminum Injections Age (Weeks) [3].
(2x 50mcg/kg)

National Vaccine Information Center
Advocacy Portal
NVIC.org & NVICAdvocacy.org



Vaccination and Health: Weighing the Risks


Unlike prescription drugs administered to the sick, vaccines are
pharmaceutical products primarily administered to healthy people.
Like prescription drugs, vaccines carry two risks: first, vaccines may
cause serious reactions, injuries or death from complications; and
second, vaccines may fail to prevent infection and transmission of
infection. NVIC supports your human right to exercise freedom of
thought, conscience and religious belief when making a vaccine
decision for yourself or minor child.

5 Vaccine Myths


Vaccine Myth 1: Most medical doctors say that vaccines do not
cause injury or death, so it must be true. FACT – Inflammation of the
brain, permanent brain damage and death have always been among
the most serious complications of vaccination. Like all pharmaceutical
products, vaccines carry a risk of harm or failure that can be greater for
some people.
Vaccine Myth 2: People who question vaccine safety are ignorant
and do not understand the science. FACT – Just the opposite is true.
Studies reveal that mothers and fathers with college or post-graduate
degrees more frequently question vaccine safety and effectiveness.
There are fewer than 40 published studies evaluating the safety of the
federally recommended vaccine schedule for children under age six.
Vaccine Myth 3: People who do not vaccinate are selfish and
don’t care about the public health. FACT – While we are all born
equal with equal rights under the law, we are not born all the same.
We each have different genes, biological susceptibilities and environ-
mental influences that affect our individual responses to diseases and
vaccines. When vaccine risks turn out to be 100 percent, some people
susceptible to vaccine harm stop vaccinating so they will not become
permanently disabled and a burden on society.

Vaccine Myth 4: Science trumps religious beliefs so religious
exemptions to vaccination should be eliminated. FACT – Science
is not infallible and doctors cannot predict who will suffer harm from
vaccination. It is a violation of human rights for government officials to
require you to be a member of an organized religion or state sanctioned
church in order to exercise freedom of conscience and religion. It is a
violation of your civil rights if you or your minor child are denied access
to an education, medical care, employment or are otherwise discrimi-
nated against or sanctioned based on your vaccination status.
OVER »

National Vaccine Information Center
Advocacy Portal
NVIC.org & NVICAdvocacy.org


» CONTINUED FROM FRONT
Vaccine Myth 5: It is ethical for government to sacrifice the few
for the many. FACT – Based on hedonism and a mathematical
equation, this philosophy is called utilitarianism. It was discredited as
a pseudo-ethic in 1947, when the ethical principle of informed consent
to medical risk taking was defined as a human right and globally
recognized as central to the ethical practice of medicine. Public health
laws using the utilitarian rationale to force vaccination are unethical
because they violate freedom of conscience and the informed consent
principle.


No Liability? No Vaccine Exemptions?
No Vaccine Mandates.



In 1986, Congress acknowledged vaccines can injure and kill and
passed the National Childhood Vaccine Injury Act, which partially
shielded drug companies from vaccine injury lawsuits. Since then, more
than $3.5 billion in federal vaccine injury compensation has been award-
ed to children and adults harmed by government mandated vaccines.
In 2011, the U.S. Supreme Court declared that government licensed and
recommended vaccines are ‘unavoidably unsafe” and effectively banned
all vaccine injury lawsuits. Seat belt manufacturers have product liability,
but vaccine manufacturers do not, and neither do doctors, employers,
and government officials punishing Americans opposing forced use of
liability-free vaccines that carry a risk of injury, death and failure.
Since the Supreme Court shielded the pharmaceutical industry from
liability for vaccine harm, lobbyists for drug companies, medical trade
associations and public health officials have lobbied state legislatures
to remove vaccine exemptions from state vaccine laws. NVIC opposes
mandatory vaccination laws without flexible medical, religious and
conscience exemptions that protect the human right to exercise freedom
of conscience, religion and informed consent to medical risk taking.



Learn more at NVIC.org
Become a vaccine choice advocate in your state. Use the
free NVIC Advocacy Portal at NVICAdvocacy.org
to defend your human and civil rights.


References for this information can be accessed
at http://tinyurl.com/nvicvaccinemyths

Copyright © NVIC 2016 – All Rights Reserved

Reference Links (for live links, go to http://avoiceforchoice.org/20-vaccine-facts/)

1. http://www.nvic.org/Vaccine-Laws/1986-Vaccine-Injury-Law.aspx; http://www.nvic.org/NVIC-Vaccine-
News/March-2011/No-Pharma-Liability--No-Vaccine-Mandates-.aspx
2. U.S. Public Health Service Act. Part F – Licensing- Biological Products and Clinical Laboratories. Subpart 1 –
Regulation of Biological Products. Sec. 351,Pg. 282
http://www.fda.gov/RegulatoryInformation/Legislation/ucm149278.htm
3. http://www.cdc.gov/vaccines/programs/vfc/awardees/vaccine-management/price-list/;
http://www.hrsa.gov/vaccinecompensation/FAQ/vicpfactsheet.pdf;
http://www.hrsa.gov/vaccinecompensation/data/statisticsreport.pdf
4. http://vaxtruth.org/2011/08/vaccine-ingredients/
5. https://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/b/excipient-table-2.pdf
6. https://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/b/excipient-table-2.pdf
7. http://www.medscape.com/viewarticle/844128
8. https://www.youtube.com/watch?v=ubSPeZAOeDs; http://www.westonaprice.org/press/studies-show-
that-vaccinated-individuals-spread-disease/
9. https://www.youtube.com/watch?v=ubSPeZAOeDs; http://whale.to/vaccines/deadly_impossibility.html;
http://tinyurl.com/linkhygiene; http://cid.oxfordjournals.org/content/38/4/591.full
10. http://articles.mercola.com/sites/articles/archive/2012/06/02/bribery-affects-vaccination-rates.aspx;
https://projects.propublica.org/docdollars/
11. https://vaers.hhs.gov/index
12. http://avoiceforchoice.org/issues/fighting-sb277/
13. http://www.huffingtonpost.com/2012/08/09/pharmaceutical-companies-marketing_n_1760380.html
14. https://wikkorg.wordpress.com/2015/06/05/robert-f-kennedy-jr-says-70-of-news-advertising-revenue-
comes-from-big-pharma/?iframe=true&preview=true
15. http://vaxxedthemovie.com; http://www.ebcala.org/unanswered-questions/inadequate-vaccine-safety-
research-and-conflicts-of-interest
16. http://www.thevaccinereaction.org/2016/02/questioning-the-safety-of-the-cdcs-childhood-vaccine-
schedule/
17. http://www.hrsa.gov/vaccinecompensation/FAQ/vicpfactsheet.pdf;
http://www.hrsa.gov/vaccinecompensation/data/statisticsreport.pdf
18. http://www.thevaccinereaction.org/2015/11/doctors-are-no-experts-on-
vaccines/, https://vactruth.com/2012/07/31/what-your-doctors-know/
19. http://www.hrsa.gov/vaccinecompensation/FAQ/vicpfactsheet.pdf
20. https://www.healthypeople.gov/





















Giving issues a voice, A Voice for Choice advocates for people’s rights to be fully informed about the composition,
quality, and short- and long-term health effects of all products that go into people’s bodies, such as food, water, air,
pharmaceuticals and cosmetics. www.AVoiceForChoice.org

If you are a parent who follows the CDC’s VACCINE schedule,

here are 20 FACTS you need to know to make an informed decision:


1. Vaccine manufacturers have NO liability (National Childhood Vaccine Injury Act of 1986), so CANNOT be
sued for injury from their product and they have no incentive to make their product as safe as possible.

2. Vaccines are not held to the same double blind gold standard of clinical testing as other pharmaceutical
drugs because they are considered biological products under the Public Health Federal Food, Drug and
Cosmetic Act. They meet the same standards as cosmetics.

3. The per vaccine Federal Excise Tax is used to pay the vaccine injured through the government-created
National Vaccine Injury Compensation Program (NVICP). $3.1 Billion has been paid to date (through 2015).

4. Vaccines contain neurotoxins (aluminum and mercury) far exceeding "safe levels" deemed by the EPA.
5. Vaccines contain cancer-causing ingredients, and have never been tested if they cause cancer, infertility or
DNA mutation (Section 13.1 of every vaccine package insert).
6. Some vaccines are made from aborted fetal cell lines. (WI-38 and MC5-5 Human Cell Fibroblasts)
7. Vaccines are not 100% effective and a vaccinated person can get the disease they were vaccinated for.
8. A vaccinated person carries the disease they were vaccinated for, "shedding" it, for up to 6 weeks.
9. The concept of herd/community immunity cannot be achieved by vaccines because vaccines are NOT
100% effective. Unlike lifetime immunity afforded by disease, vaccine-induced immunity lasts 2-10 years.
10. Doctors receive financial rewards from insurance companies for having patients fully vaccinated (~$400
per patient). They are advised NOT to share all the risks or the vaccine package inserts, so 100% informed
choices cannot be made in a doctor’s office when vaccinating.
11. Vaccine injury is under-reported. VAERS is the only way to officially report a vaccine injury and is tedious
with no incentive for a doctor to fill it out.
12. Vaccine mandates (like SB277 and SB792 in CA) literally hand over new customers to pharmaceutical
companies, and remove rights to choose what is injected into a person’s body.
13. Pharmaceutical companies spend up to 19 times more on advertising than they do on research.

14. Corporate mainstream media gets 70% of their advertising revenue from pharmaceutical companies.
15. Vaccine safety and efficacy research is not conducted by independent researchers and so is biased.
16. The full CDC recommended vaccine schedule has never been tested. Vaccinated children are the human
experiment.
17. All vaccines can cause injury or death, and there is no way to tell who will have a reaction.
18. Most doctors receive 30 MINUTES on vaccine education (that they are safe, effective and a must) during
their 8 YEARS in medical school.
19. If someone dies from a vaccine, their family will be awarded no more than $250,000. Most cases of
vaccine injury are dismissed because doctors and vaccine manufacturers deny a causation link. The
statutory time limit for filing a claim is only 2 years after death and 3 years from the time of vaccine injury.
20. The government plan “Healthy People 2020” has a goal to fully vaccinate all children and adults by 2020.
There are 217 new vaccines being created right now.

DO YOUR OWN RESEARCH BEFORE YOU VACCINATE.
This is too important to ignore.

Isn’t your baby worth the time and effort to get engaged and educated?




Giving issues a voice, A Voice for Choice advocates for people’s rights to be fully informed about the composition,
quality, and short- and long-term health effects of all products that go into people’s bodies, such as food, water, air,
pharmaceuticals and cosmetics. www.AVoiceForChoice.org

LIST OF VACCINE INGREDIENTS AND THEIR KNOWN

SIDE EFFECTS

http://www.cdc.gov/vaccines/vac-gen/additives.htm

Refer to the table of Vaccine Exipients from the CDC.

Vaccine Ingredient: Human Viruses

The viruses against which the vaccine is supposed to protect are frequently
said to be “killed”, “inactivated”, or “attenuated”. This is a myth. The main
method used to inactivate viruses is treatment with formaldehyde, whose
effectiveness is limited, and even then only temporary. Once the brew is
injected into the body, the formaldehyde is broke down by the body
potentially releasing the virus in its original state. This is intentional. It is
documented in orthodox medical literature that these living “crippled” viruses
can revert to their former virulence.

Please remember that the included viruses, and bacteria, which the vaccine
is supposed to protect against are claimed to be in “very small doses”. These
small doses are not small to the body, and these quantities are quite high
enough for the diseases to occur. When they do occur, the cases are always
severe, and sometimes fatal. Several deaths were reported in the British

medical journal, Lancet, from vaccine -induced yellow fever. A susceptible
person may succumb to infection when exposed to only a minute doses,
especially when it is injected directly into the bloodstream. Likewise, there are
other cases in which a healthy person will not succumb, even when exposed
to large doses environmentally. It is not the pathogens, but the interaction
methods between pathogens and hosts which causes diseases to appear,
and the level of their severity.

Vaccines may not manifest obvious injury, especially not immediately, but are
still likely to cause long term harm to internal organs and the immune system
given their ingredients, and their known effects.

Most disease symptoms are the visible signs of a body’s attempts to defend
itself against the infection. With disease injections, many important defences
in the digestion path and mucous membranes are bypassed.



Vaccine Ingredient: Aborted Human Fetus Tissue and Human Albumin

From a health perspective, the tissues from another human (not just animals)
are still foreign, and therefore toxic to the body. One industry -friendly web
site matter--of--factly boasted, “The cells reproduce themselves, so there is
no need to abort additional fetuses to sustain the culture supply. Viruses are
collected from the diploid cell cultures and then processed further to produce
the vaccine itself”. The Liberty Counsel reported, “You may be surprised to
learn that some vaccinations are derived from aborted fetal tissue. Vaccines
for chicken pox, Hepatitis-A, and Rubella were produced solely from aborted
fetal tissue”.


MRC-5, DNA, MRC-5 Cellular Protein, Human Serum Albumin (4 different
ingredients)

All of these derive from either human tissue or human blood.


MRC-5, MRC-5 Cellular Protein


To explain MRC-5, let’s look at a brief history before MRC-5 came about. In
1964, during an outbreak of Rubella, some doctors urged women who had
been exposed to the Rubella virus to abort their pregnancy. (Why? Rubella
is an extremely mild virus [see:
http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0002541/]. Most people
don’t show any symptoms, especially children, some may get a rash all over
their body. Rubella becomes dangerous when a pregnant woman is exposed
to the virus because it has the potential to cause severe abnormalities in the
child.) From one of these aborted children that had been exposed to Rubella
Virus, doctors developed a virus strain that became known as RA/27/3 —
Rubella; Abortus; 27th aborted fetus; 3rd tissue explant. In other words, it
took 26 aborted infants to get the right strain. The virus was then cultivated
on the lung tissue of another aborted child, and this child became known as
WI-38 — Winster Institute 38). WI -38 was an infant girl at 3 months
gestation. What makes this seem somewhat ridiculous is that the Japanese,
years before the first aborted infant was used to extract the Rubella virus,
proved that the virus can be taken from a *living* child simply by swabbing
their throat.


In the 1970′s, a second human cell line was created from an infant boy at 14
weeks gestation and became known as MRC-5.


WI-38 and MRC-5 have become the most used cell lines to make
vaccinations. Labs currently use these 2 cell lines, as well as new sources
(a.k.a new aborted infants) to create new vaccines.

The use of tissue from aborted infants has caused heated debate because it
is ethically questionable. Pro-life groups, which include many churches and
parents whose morals condemn profiting from aborted infants, continue to
fight the pharmaceutical companies to produce vaccines that do not contain
this tissue. And the thing is, it’s possible. Vaccines can be made from other
sources.


DNA


DNA is harvested from aborted infants. It is used as adjuvant in vaccines. In
vaccines, 100,000,000 bits and strands of human dna are allowed per dose.
Again, we encounter the issue of the ethical dilemma for this issue.

Human Serum Albumin


Human Serum Albumin is a stabilizing protein made from human blood
donated by screened donors. We already discussed above why injecting a
protein directly into the body is dangerous.


With that aside, let’s look at the points we reach regarding these 4 different
ingredients:


We have human DNA, human cell lines from aborted infants, and protein
from human blood in 23 of our vaccines. When we need a blood transfusion,
or a blood donation of some kind, what is absolutely required? A match,
correct? For example, if a person with type O blood receives type A+ blood,
the outcome is fatal. There are rules of science that cannot be crossed
regarding DNA and blood. It is imperative to be tested when receiving any
type of tissue or blood to ensure that a fatal blood or tissue type isn’t put into
your body. So may I ask: How many of you or your children were given a
blood test before receiving vaccinations? We all know the answer to that.
It doesn’t happen. The outcome to mixing and NOT matching human blood
and tissue with other humans can be virtually disastrous. Remember that
every one of those 4 ingredients have human DNA in them. Even after the
protein is extracted from human blood, DNA remains.


There was a recent study done by Dr. Helen Ratajczak called “Theoretical
aspects of autism: Causes–A review.” In this study, Dr. Ratajczak studied the
problems associated with injecting human tissue into another person. Please
see the CBS report on this study. In this CBS report it says:


Ratajczak also looks at a factor that hasn’t been widely discussed: human
DNA contained in vaccines. That’s right, human DNA. Ratajczak reports that
about the same time vaccine makers took most thimerosal out of most
vaccines (with the exception of flu shots which still widely contain thimerosal),
they began making some vaccines using human tissue. Ratajczak says

human tissue is currently used in 23 vaccines. She discusses the increase in
autism incidences corresponding with the introduction of human DNA to MMR
vaccine, and suggests the two could be linked. Ratajczak also says an
additional increased spike in autism occurred in 1995 when chicken pox
vaccine was grown in human fetal tissue.


Why could human DNA potentially cause brain damage? The way Ratajczak
explained it to me: “Because it’s human DNA and recipients are humans,
there’s homologous recombinaltion tiniker. That DNA is incorporated into the
host DNA. Now it’s changed, altered self and body kills it. Where is this most
expressed? The neurons of the brain. Now you have body killing the brain
cells and it’s an ongoing inflammation. It doesn’t stop, it continues through the
life of that individual.”




Vaccine Ingredient: Formaldehyde

Formaldehyde is most commonly used by funeral centres for dead bodies.

This is used in vaccines as a tissue fixative, and a preservative.

Formaldehyde is oxidized to become formic acid. Formic acid is the main
ingredient of bee and ant venom. Concentrated, it is corrosive and an irritant.
While absorbing the oxygen of the body, it may lead to acidosis, nerve, liver,
and kidney damage.


Formalin is an aqueous, or watery, form of Formaldehyde.


• Formaldehyde is toxic and is known to cause cancer. The
International Agency for Research on Cancer (IARC) classifies
formaldehyde as a human carcinogen [International Agency for
Research on Cancer (June 2004). IARC Monographs on the Evaluation
of Carcinogenic Risks to Humans Volume 88 (2006): Formaldehyde, 2-
Butoxyethanol and 1-tert-Butoxypropan-2-ol. Retrieved June 10, 2011,
from:http://monographs.iarc.fr/ENG/Monographs/vol88/index.php].

• In 2011, the National Toxicology Program, an interagency program of
the Department of Health and Human Services, named formaldehyde
as a known human carcinogen in its 12th Report on
Carcinogens [National Toxicology Program (June 2011). Report on
Carcinogens, Twelfth Edition. Department of Health and Human
Services, Public Health Service, National Toxicology Program.
Retrieved June 10, 2011, from: http://ntp.niehs.nih.gov/go/roc12].

According to the National Research Council:


Fewer than 20% but perhaps more than 10% of the general population may
be susceptible to formaldehyde allergies and may react acutely at any
exposure level.


Formaldehyde is ranked as one of the most hazardous compounds on
ecosystems and human health, according to the Environmental Defense
Fund. These findings are for environmental exposure, and therefore, the
dangers are much greater for the formaldehyde included in vaccines, since it
is injected directly into the blood.


The known side effects of formaldehyde are:


 Eye, nasal, throat and pulmonary irritation
 Acute sense of smell due to altered tissue proteins
 Anaemia
 Asthma
 Apathy
 Alters tissue proteins

 antibodies formation
 Blindness
 Blood in urine
 Blurred vision
 body aches
 Pain
 Bronchial spasms
 Bronchitis
 Burns in sinus area and throat
 Cardiac impairment
 Palpitations and arrhythmias

 Central nervous system depression
 Changes in higher cognitive functions
 Chemical sensitivity
 Chest pains and tightness
 Chronic vaginitis; colds
 Coma

 Conjunctivitis
 Constipation
 Convulsions

 Corneal erosion
 Death

 Destruction of red blood cells
 Depression
 Dermatitis
 Diarrhoea
 Difficulty concentrating
 Disorientation and dizziness
 Ear aches
 Eczema

 Emotional upsets
 Ethmoid polyps
 Fatigue
 Fecula bleeding
 Foetal asphyxiation
 Flu-like or 'common cold' illness
 Frequent urination with pain

 Gastritis
 gastrointestinal inflammation
 Headaches
 Haemolytic anaemia
 Haemolytic haematuria
 Hoarseness
 Hyperactive airway disease
 Hyperactivity
 Hypomenstrual syndrome

 Immune system (allergen) sensitizer
 Impaired (short) attention span
 Impaired capacity to attain attention
 Inability or difficulty swallowing
 Inability to recall words and names
 Inconsistent IQ profiles
 Inflammatory diseases of the reproductive organs

 Intestinal pain
 Intrinsic asthma
 Irritability
 Jaundice
 Joint pain
 Joint swelling
 Kidney pain
 Laryngeal spasm

 Loss of memory

 Loss of sense of smell
 Loss of taste

 Malaise
 Menstrual and testicular pain
 Menstrual irregularities
 Metallic taste
 Muscle spasms and cramps
 Nasal congestion
 Crusting and mucosa inflammation
 Nausea

 Nosebleeds
 Numbness and tingling ofthe forearms and finger tips
 Partial laryngeal paralysis
 Pneumonia,and Pulmonary Oedema
 Reduced bodytemperature
 Retarded speech pattern
 Ringing or tingling in the ear

 Schizophrenic- type symptoms
 Sensitivity to sound
 Shock
 Short term memory loss
 Shortness of breath
 Skin lesions
 Sneezing
 Sore throat
 Spacey feeling

 Speaking difficulty
 Sterility
 Swollen glands
 Tearing
 Excessive Thirst
 Tracheitis
 Tracheobronchitis

 UTI
 Vertigo
 Vomiting blood
 Vomiting
 Wheezing and Lung Complication


Vaccine Ingredient: Mercury/Thimerosal

Thimerosal is a compound made up of approximately 50% mercury.

Thimerosal is used as a preservative in vaccines to help prevent bacteria
growth in multi-use vaccines. It is also used in the creation process of a
vaccine, and then through a purification process it is “removed” and only
“trace” amounts are left. Refer below for TRACE AMOUNTS


The toxicity of mercury has been repeatedly ignored in the area of vaccines
by the medical establishment and oversight agencies. Mercury is the second
most poisonous element known to mankind (second only to uranium and its
derivatives). Brain neurons rapidly and permanently disintegrate in the
presence of mercury within 30 minutes of exposure. Mercury is also known to
change a body’s chromosomes.



The U.S. has known about the potential problems of Thimerosal (the
preservative in vaccines that contains mercury) for many years. The World
Health Organization voiced concerns about it in 1990.

Mercury is a cumulative poison, which means a body has difficultly
removing it, and that levels of it in the body will grow significantly over time.
Enormous amounts of mercury can accumulate over a lifetime. During a
typical day of routine vaccines, infants sometimes receive the same amount
of mercury as the absolute maximum set by the World Health Organization
for 3 months of adult exposure.

The following was taken from a website affiliated with the National
Institutes for Health detailing the effects of mercury exposure: “Symptoms of
high exposure to this class of mercury based compounds include: aphthous,
stomatitis, satarrhal gingivitis, nausea, liquid stools, pain, liver disorders,
injuries to the cardiovascular system and hematopoietic system, deafness
and ataxia, death, headache, paresthesia of the tongue, lips, fingers and
toes, other non-specific dysfunctions, metallic taste, slight gastrointestinal
disturbances, excessive flatus and diarrhea may occur. Acute poisoning may
cause gastrointestinal irritation and renal failure. Early signs of severe
poisoning include fine tremors of extended hands, loss of side vision, slight
loss of coordination in the eyes, speech, writing and gait, inability to stand or
carry out voluntary movements, occasional muscle atrophy and flexure
contractures, generalized myoclonic movements, difficulty understanding
ordinary speech, irritability and bad temper progressing to mania, stupor,
coma, mental retardation in children, skin irritation, blisters and dermatitis.
Other symptoms include chorea, athetosis, tremors, convulsions, pain and
numbness in the extremities, nephritis, salivation, loosening of the teeth, blue
line on the gums, anxiety, mental depression, insomnia, hallucinations and
central nervous system effects. Exposure may also cause irritation of the
eyes, mucous membranes and upper respiratory tract.”

Complete intolerance to Thimerosal, the mercury containing preservative,
is known to develop from previous vaccines. The vaccines stimulate the
immune system and cause sensitization. The effects of mercury differ
between inorganic, organic, and metallic mercury compounds. The neurologic
toxicity symptoms caused by mercury compounds have a delayed onset after
exposure, so few, if any of these symptoms will be noticed at the time of
exposure. This explains the suspected long-term neurological symptoms of
learning disabilities and behavior disorders associated with vaccines, which
did not exist in previous generations.




Thimerosal - TRACE AMOUNTS



Next, let’s discuss what “trace amounts” means. (If you notice in the
document above next to many of the “Thimerosal”‘s, there is an asterisk next
to it. The asterisk notates that ” *Where “thimerosal” is marked with an
asterisk (*) it indicates that the product should be considered equivalent
to thimerosal-free products.”)




So the fact that those vaccines containing thimerosal with an asterisk beside
it virtually says the same thing and is extremely misleading. They should be
“considered equivalent to thimerosal-free products” gives the illusion that
there is no thimerosal in vaccines, or at least not enough to have to worry
about. But remember, Many “well-child” check-ups include up to 8 vaccines
in one sitting.


First, I urge you to read this article: Is There Thimerosal in the Flu
Vaccine?


Within this article is a link to the CDC article declaring that yes, the flu
vaccine contains mercury. Please read this very carefully and with the same
skepticism I would hope you apply to everything you read online (including
this website):
http://www.cdc.gov/FLU/ABOUT/QA/thimerosal.htm


Note that the CDC uses terminology indicating that even in the vaccines that
are labeled “preservative-free” THIMEROSAL IS USED IN THE
MANUFACTURING PROCESS. The CDC states that the amount is so small
and by the time the process is finished, it is untraceable. This is different from
stating that IT IS NOT THERE. This is the same type of semantic trickery that
has been played for years. Nothing has changed.

So how much does “trace” mean? According to the CDC, it says less than or
equal to 0.3mcg per dose. Sailhome.org does a nice job of putting this into
perspective:


• 2 ppb mercury is the mandated limit in drinking water


• 200 ppb mercury in liquid waste renders it a toxic hazard

• 25,000 ppb is found in infant flu shots


• 50,000 ppb is found in regular flu shots — recommended for children,
pregnant women, the elderly…


Also the math on how many ppb in a “thimerosal free” vaccine:


0.3 mcg / 0.5mL =
0.3 mcg / .0005L =
…3,000 mcg / 5L =
600 mcg / L
1 mg/KG = 1 PPM (formal definition of PPM)
1 L = 1 KG (density of water or saline solution)
1 mcg/L = 1 PPB (because 1 KG and 1 L of water are equivalent)
THEREFORE:
600 mcg / L =
600 ppb Thimerosal in the “thimerosal-free” vaccine


Flu vaccine has “only” 25 mcg Thimerosal. The shot is 0.5mL. Let’s do some
math:
25 mcg / 0.5mL =
25 mcg / .0005L =
250,000 mcg / 5L =
50,000 mcg / L
1 mcg / L = 1 ppb, therefore
The shot has 50,000 ppb of Thimerosal


Remember that 2 ppb mercury is the mandated limit in drinking water and
normally 200 ppb would label something a toxic hazard.

After we find all of this information out, we have to ask ourselves: Why is
mercury dangerous??



***Notice that mercury doesn’t only stunt neurological growth, it actually
reverses it, or destroys it.

Vaccine Ingredient: Antifreeze

Antifreeze (ethylene glycol) is an ingredient of the polio vaccine. It is
classified as a "very toxic material". It would take less than a tablespoonful to
kill a 20-pound dog with this substance. Pet owners are generally very wary
around this dangerous substance, knowing that only a small amount is fatal. I
can only imagine the effects that this has on the human body when directly
injected into the blood stream.

Antifreeze can eventually lead to kidney, liver, blood and central nervous
system (CNS) disorders. It is quite harmful and likely fatal if swallowed.
Effects include behavioral disorders, drowsiness, vomiting, diarrhoea, visual
disturbances, thirst, convulsions, cyanosis, rapid heart rate, CNS stimulation,
depression, cardiopulmonary effects, kidney disorders. It can also lead to
liver and blood disorders. It produces reproductive and developmental effects
in experimental animals.


Vaccine Ingredient: Aluminium

Aluminum is a suspected carcinogen. It is a cardiovascular or blood toxicant,
neurotoxicant, and respiratory toxicant. It has been implicated as a cause of
brain damage, and is a suspected factor in Alzheimer’s Disease, dementia,
convulsions, and comas. It has been placed on at least 2 federal regulatory

lists.

Aluminum is present in many things around us. It’s in food, air, water, and
soil and is said to be harmless when swallowed because it doesn’t absorb
into the body when consumed. Aluminum is put into vaccines as an
adjuvant to help them “work better” or to “enhance” them. So what is the
concern about injecting aluminum into the blood stream?

According to the FDA:


“Aluminum may reach toxic levels with prolonged parenteral administration
[this means injected into the body] if kidney function is impaired . . . Research
indicates that patients with impaired kidney function, including premature
neonates [babies], who received parenteral levels of aluminum at greater
than 4 to 5 micrograms per kilogram of body weight per day, accumulate
aluminum at levels associated with central nervous system and bone toxicity
[for a tiny newborn, this toxic dose would be 10 to 20 micrograms, and for an
adult it would be about 350 micrograms]. Tissue loading may occur at even
lower rates of administration.” [Department of Health and Human Services,

Food and Drug Administration, Document NDA 19-626/S-019, Federal Food,
Drug and Cosmetic Act for Dextrose Injections.]


And also:


“Aluminum content in parenteral drug products could result in a toxic
accumulation of aluminum in individuals receiving TPN therapy. Research
indicates that neonates [newborns] and patient populations with impaired
kidney function may be at high risk of exposure to unsafe amounts of
aluminum. Studies show that aluminum may accumulate in the bone, urine,
and plasma of infants receiving TPN. Many drug products used in parenteral
therapy [injections] may contain levels of aluminum sufficiently high to cause
clinical manifestations [symptoms] . . . parenteral aluminum bypasses the
protective mechanism of the GI tract and aluminum circulates and is
deposited in human tissues. Aluminum toxicity is difficult to identify in infants
because few reliable techniques are available to evaluate bone metabolism in
. . . infants . . . Although aluminum toxicity is not commonly detected clinically,
it can be serious in selected patient populations, such as neonates
[newborns], and may be more common than is recognized.” [Department of
Health and Human Services, Food and Drug Administration, Document 02N-
0496, Aluminum in Large and Small Volume Parenterals Used in Total
Parenteral Nutrition. Available online at:
http://www.fda.gov/ohrms/dockets/98fr/oc0367.pdf]


So basically from those documents we learn that if a premature baby
receives more than 10 mcg of aluminum in an IV, it can accumulate in their
bones and brain, and can be toxic.

The FDA maximum requirements for aluminum received in an IV is 25
mcg per day. The suggested aluminum per kg of weight to give to a person
is up to 5mcg. (so a 5 pounds baby should get no more than 11mcg of
aluminum.) Anything that has more than 25 mcg of aluminum is *supposed*
to have a label that says:


WARNING: This product contains aluminum that may be toxic. Aluminum
may reach toxic levels with prolonged parenteral administration if kidney
function is impaired. Premature neonates are particularly at risk because their
kidneys are immature, and they require large amounts of calcium and
phosphate solutions, which contain aluminum.


Research indicates that patients with impaired kidney function, including
premature neonates, who receive parenteral levels of aluminum at greater
than 4 to 5 [micro]g/kg/day accumulate aluminum at levels associated with
central nervous system and bone toxicity. Tissue loading may occur at even
lower rates of administration.

[http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?fr=
201.323]


– Vaccines, for some reason, are not required to have this label and also are
not required to follow the maximum dosage of 25 mcg.


So doing some math — the following are examples of weight with their
corresponding maximum levels of aluminum, per the FDA:

8 pound, healthy baby: 18.16 mcg of aluminum


15 pound, healthy baby: 34.05 mcg of aluminum


30 pound, healthy toddler: 68.1 mcg of aluminum


50 pound, healthy child: 113 mcg of aluminum


150 pound adult: 340.5 mcg of aluminum

350 pound adult: 794.5 mcg of aluminum


So how much aluminum is in the vaccines that are routinely given to
children?


• Hib (PedVaxHib brand only) – 225 mcg per shot
• Hepatitis B – 250 mcg
• DTaP – depending on the manufacturer, ranges from 170 to 625 mcg
• Pneumococcus – 125 mcg
• Hepatitis A – 250 mcg
• HPV – 225 mcg
• Pentacel (DTaP, HIB and Polio combo vaccine) – 330 mcg
• Pediarix (DTaP, Hep B and Polio combo vaccine) – 850 mcg



At birth, most children are given the hepatitis B vaccination. The amount of
aluminum in the Hepatitis B vaccine alone is almost 14 TIMES THE
AMOUNT OF ALUMINUM THAT IS FDA-APPROVED.

At well-child check-ups, it’s common for 2 month, 4 month, 6 month etc.,
appointments to include up to 8 vaccinations that add up to more than 1,000
mcg of aluminum. Look at the chart above and notice that that amount isn’t
even safe for a 350 pound adult. And many children get up to 8 vaccinations
a visit several times a year!

According to the FDA and the AAP (American Academy of Pediatrics), what
happens if a child receives more than the maximum required dose of
aluminum?


• Aluminum builds up in the bones and brain and can be toxic.
• Aluminum can cause neurological harm.
• Aluminum overdose can be fatal in patients with weak kidney’s or
kidney disorders or in premature babies. (How many children are tested
to see if their kidney’s are functioning properly before they are
vaccinated? Could this also be why the Hepatitis B shot, given to
infants at birth, has been linked to SIDS? Neonatal Deaths After Hep B
vaccination.)



[Aluminum Toxicity in Infants and Children, Committee on Nutrition,American
Academy of Pediatrics, Pediatrics Volume 97, Number 3 March, 1996, pp.
413-416]



Vaccine Ingredient: 2-Phenoxyethanol


This is a suspected carcinogen. A developmental and reproductive toxicant. It
is also a metabolic poison, which means that it interferes with the metabolism
of all cells. This is the primary factor in the formation of cancer cells. It is
capable of disabling the immune system’s primary response. It also contains
phenol (see below for explanation).


2-Phenoxyethoanol is used as an antibacterial agent in vaccines. According
to the MSDS (Material Safety Data Sheet), we find that it is toxic if swallowed,
inhaled, absorbed through the skin, it is a severe skin and eye irritant, and it
may cause reproductive defects
[http://www.sciencelab.com/msds.php?msdsId=9926486]. According to the
EPA data sheets, it has shown to cause chromosomal changes and genetic
mutations in tests, as well as testicular atrophy and interference
with reproductivity in mice [http://www.epa.gov/ttn/atw/glycol2000.pdf].

The known side effects of 2-Phenoxyethanol exposure are:


• Headache
• Shock
• Convulsions
• Weakness
• Kidney damage

• Cardiac failure
• Kidney failure
• Death



Vaccine Ingredient: Phenol

This is a suspected carcinogen, and a cardiovascular and blood toxicant.
Also known as carbolic acid; this is a developmental toxicant, gastrointestinal
or liver toxicant, kidne toxicant, neurotoxicant, respiratory toxicant, skin and
sense organ toxicant. It has been placed on at least 8 federal regulatory lists.


Vaccine Ingredient: Methanol

This is a volatile, flammable, poisonous liquid alcohol. In industry, it is used
as a solvent, and an antifreeze compound in fuel. In the body it is
metabolized into formaldehyde (as described earlier). Whilst it can be found
naturally in the pectin that is present in some common fruits, the naturally
occurring version is only in minute quantities, and the natural form is not
known to cause harmful effects.


Vaccine Ingredient: Borax (sodium tetraborate decahydrate)


Traditionally used as a pesticide and ant killer. It is suspected to be a
cardiovascular or blood toxicant, endocrin toxicant, gastrointestinal or liver
toxicant, and neurological toxicant. It was found to cause reproductive
damage and reduced fertility rates in studies on rats. It is already banned in
foods in the United States, but astonishingly, it is still allowed for direct
injection into the blood through vaccines. It is toxic to all cells, and has a slow
excretion rate through the kidneys. Kidney retention and toxicity are the
greatest. It has a cascading effect, causing liver degeneration, cerebral
edema, and gastroenteritis.

“A single vaccine given to a 6 pound infant is the equivalent of giving a 180
lb. adult 30 vaccines in one day.”
― Dr. Boyd Haley


Vaccine Ingredient: Glutaraldehyde

Glutaraldehyde is always toxic, causing severe eye, nose, throat and lung
irritations, along with headaches, drowsiness, and dizziness. The effects

mirror the chemical warfare agent known as nerve gas. It is poisonous if
ingested, and known to cause birth defects in experimental animals. The
effects of direct injection into the blood to bypass the process of ingestion are
unknown. It is often used to clean medical equipment. In hospital accidents
involving environmental exposure, it has been known to cause the following
symptoms:

• Throat and lung irritation
• Asthma, asthma-like symptoms, and breathing difficulty
• Nose irritation, sneezing, and wheezing
• Nosebleed
• Burning eyes and conjunctivitis
• Rash-contact and/or allergic dermatitis
• Staining of the hands (brownish or tan)
• Hives
• Headaches
• Nausea


Vaccine Ingredient: MSG (Monosodium Glutamate)

Monosodium Glutamate is a synthetic flavor enhancer. In a 1995 report by
the Federation of American Societies for Experimental Biology, two groups of
people were defined as intolerant of MSG. This includes those who eat large
quantitie of MSG (it is used in lots of processed foods as a flavor enhancer),

and those with “poorly controlled asthma”. Our research indicates that
anyone can suffer after consuming Monosodium Glutamate. In the 1995
report, which was contracted by the FDA, there was public admission that
MSG yields the following symptoms:

• Burning sensations in the back of the neck, forearms and chest
• Numbness in the back of the neck, radiating to the arms and back
• Tingling, warmth, and weakness in the face, temples, upper back, neck and
arms
• Facial pressure or tightness
• Chest pain
• Headache
• Nausea
• Rapid heartbeat
• Bronchospasm (difficulty breathing) in MSG -intolerant people with asthma
• Drowsiness
• Weakness
• Migraine headaches
• Sleeping disorders
• Irritable Bowel Syndrome

• Asthma
• Diabetes
• Alzheimer’s disease
• Lou Gehrig’s disease
• Attention Deficit Disorder
• Seizure
• Stroke
• Anaphylactic reaction

Note that this is the short-list (the one with side effects the FDA actually
admits), and it does not consider the highe toxicity of direct injection into the
blood. The long list, which is about 15 times longer, includes heart attacks,
especially in young people with magnesium deficiencies. Injections of
glutamate in laboratory animals have resulted in rapid damage to nerve cells
in the brain. MSG is in a special class of chemicals called excitotoxins, which
are known to directly attack brain cells. In 1978, MSG was banned from baby
foods and other baby products for infants who were less than one year of
age, because the American Academy of Pediatrics and the National
Academy of Sciences expressed concerns. It is now being used in these
products again, along with vaccines.


Vaccine Ingredient: Genetically Modified Yeast

Yeast extract is a common name used for various forms of processed yeast.

Many people have yeast allergies, and vaccines can induce an anaphylactic
response after being vaccinated due to the yeast.

Aside from that, ALL yeast extract contains MSG. Many people have either
an allergy or a sensitivity to MSG.


This is in the Hepatitis B Vaccine. Given the controversy over the ingestion of
genetically modified foods, how much more dangerous do you think the direct
injection of them is? What are the future consequences of this genetic
experimentation against our children? Normal yeast that grows throughout
the tissues is already known to be the root cause of countless ailments which
can last for years, and in the rare cases when it is proper diagnosed, these
are called yeast infections. Yeast overgrowth directly attacks the immune
system, and cripples the body’s ability to remove wastes, toxins, and absorb
nutrients categorically. The standard treatment for it with antibiotics often
actually strengthens these infections in the long- term by killing more of the
beneficial flora which normally keeps yeast overgrowth in check.

Vaccine Ingredients: Amino Acids and Proteins (Albumin is also a type
of protein):

What are amino acids? Put simply, amino acids are the building blocks of
proteins in our bodies and they make up over 3/4 of the human body. There
are 20 amino acids found naturally in the body and 8 that are considered
“essential” for humans because our bodies cannot create them naturally, and
therefore must be taken into our bodies by diet. (This becomes a *great*
selling point for certain diets or food products).


So injecting amino acids into the body by way of vaccination is good, yes?
Wrong.


• Vaccines are called antigens — “A toxin or other foreign substance that
induces an immune response in the body, especially the production of
antibodies.” Antigens are made from foreign proteins. These foreign
proteins are produced from animals (like cows, monkey’s and chickens)
and also humans (human cells from aborted fetuses.)
• Foreign proteins (in order to be beneficial to the body) need to first be
digested in the GI tract. Protein is broken down into amino acids during
the digestion process.

“When we eat protein it is broken down into its constituent amino acids…if a
foreign animal protein makes it into our bloodstream without having being
broken down this can set up an autoimmune type response…By injecting
things never meant to be in the body we are not only bypassing body
defenses but wrongly activating other defenses.” — Dr. Robyn Crosford


So what’s the outcome if you inject amino acids and/or foreign animal and
human protein into the body instead of first digesting the proteins to make
amino acids naturally?
• Auto-immune disorders like Addison’s disease, celiac disease –
sprue (gluten-sensitive enteropathy), dermatomyositis, Graves disease,
Hashimoto’s thyroiditis, multiple sclerosis, myasthenia gravis,
pernicious anemia, reactive arthritis, rheumatoid arthritis, Sjogren
syndrome, systemic lupus erythematosus, type I diabetes etc.
• Food allergies or food sensitivities associated with eggs, gluten,
peanuts, milk, etc.



Vaccine Ingredients: Egg Protein

We already discussed under Amino Acids why injecting protein directly into
the body is harmful. Aside from that, individuals allergic to eggs can have a

serious reaction to vaccines that contain egg protein. What’s interesting is
that many parents don’t know that vaccines contain egg products, and
doctor’s virtually never reveal that information (if they are actually aware
themselves), even if they know that vaccines contain egg products. When a
child with an egg allergy has a reaction to a vaccine, doctor’s often deny the
fact that it’s even a *possibility* that the vaccine caused the reaction.




Vaccine Ingredients: Sulfate and Phosphate Compounds

These can trigger severe allergies in children which may last throughout their
lives to permanently impair their immune systems.


Vaccine Ingredient: Ammonium Sulfate

This is another carcinogen. Ammonium sulfate is prepared by mixing
ammonia with sulfuric acid. It is used as a chemical fertilizer for alkaline soils
to lower the pH of the soil. In the body, it stresses the immune system by
causing acidosis.

Ammonium sulfate is also a gastrointestinal (liver) toxicant, neurotoxicant,
and respiratory toxicant.


Vaccine Ingredient: Gentamicin Sulfate

This is a strong antibiotic, which is often used for life- threatening illnesses
(eg. pneumonia).

Known side effects:

• Muscle twitching
• Numbness
• Seizures
• Increased Blood Pressure
• Alopecia
• Purpura
• Pseudotumor cerebri
• Photosensitivity
• Transient irritation
• Burning
• Stinging
• Itching

• Inflammation
• Angioneurotic edema
• Urticaria
• Vesicular and maculopapular dermatitis
• Mydriasis
• Conjunctival paresthesia
• Conjunctival hyperemia
• Nonspecific conjunctivitis,
• Conjunctival epithelial defects
• Lid itching and swelling
• Bacterial/fungal corneal ulcers




Vaccine Ingredient: Neomycin Sulfate

When researching this, we discovered the neurotoxicity of neomycin sulfate
following oral use as an antibiotic. I can only wonder about what damage this
causes when injected directly into the blood of infants. It interferes with
vitamin B6 absorption, which is the cause of a rare form of epilepsy, and
mental retardation. Adult patients given neomycin as an antibiotic are
typically placed under close clinical observation (ie. hospitalized), so that
intensive care intervention is immediately available. Neurotoxicity has been
reported, along with nephrotoxicity, and permanent bilateral auditory

ototoxicity. Sometimes vestibular toxicity is present in patients with normal
renal function when treated with higher or longer doses than recommended.


Vaccine Ingredient: Tri(n)butylphosphate

This is yet another carcinogen. This is a kidney toxicant and a neurotoxicant.
It is more hazardous than most chemicals in 2 out of 3 ranking systems, on at
least 1 federal regulatory list.


Vaccine Ingredient: Polymyxin B

This is another antibiotic. Injection of this is generally avoided by doctors
(except in the case of vaccines), due to severe pain at injection sites,
particularly in infants and children.

Other Known Side Effects:

• Albuminuria

• Cylindruria
• Azotemia
• Rising blood levels without any increase in dosage.
• Facial flushing
• Dizziness progressing to ataxia
• Drowsiness
• Peripheral paresthesias: circumoral and stocking-glove
• Apnea
• Signs of meningeal irritation with intrathecal administration


Vaccine Ingredient: Polysorbate 20 /80 Emulsifier

This is a suspected carcinogen. It is a known skin and sense organ toxicant.
It is verified as a cancer agent in animals.

Polysorbate 80 accelerated the matu- ration of the female rats, damaged the
vagina and womb lining, caused significant hormonal changes, se- vere ovary
deformities and ultimately rendered the young female rats infertile.


Vaccine Ingredient: Sorbitol Sweetener

Diabetic retinopathy and neuropathy may be related to excess sorbitol in the
cells of the eyes and nerves; leading to blindness. This is another suspected

carcinogen. Sorbitol is a gastrointestinal and liver toxicant.


Vaccine Ingredient: Polyribosylribitol

This is an experimental artificial sweetener. Actually the experimentation is
ongoing ― in children that is, without the knowledge or consent of their
parents.


Vaccine Ingredient: Beta- Propiolactone

Documented as a verified carcinogen. It is a gastrointestinal (liver) toxicant,
respiratory toxicant, skin toxicant, and sense organ toxicant. More hazardous
than most chemicals; earning a 3 out of 3 in ranking systems. It appears on at
least 5 federal regulatory lists. It is ranked as one of the most hazardous
compounds to humans.


Vaccine Ingredient: Amphotericin B

This can cause irreversible kidney damage, and mild liver failure. It has been
known to produce severe histamine (allergic) reactions. There are several
reports of anemia and cardiac failure. According to the MME definition it is, “a
drug used to treat fungus infections. Known allergy to this drug prohibits use.
Side effects include blood clots, blood defects, kidney problems, nausea and
fever. When used on the skin, allergic reactions can occur”.


Vaccine Ingredient: Benzethonium Chloride

Benzethonium Chloride (referred to as “BC”) is an anti-microbial agent used
as a preservative in some vaccines. There has been no testing done on
humans to find out information regarding the injection of BC into the blood
stream. I have been searching for over a year with no luck in finding any
such information. What has been documented about BC under the MSDS
(Material Safety Data Sheet) under section 11 is that it is toxic when inhaled
or ingested and is also hazardous to human skin. Based on animal
testing, it may cause mutations in genetic information and also be
carcinogenic (cause cancer).


The known side effects of ingesting BC are (according to it’s MSDS):


• Seizures
• Coma
• Respiratory depression
• Central Nervous System Depression
• Convulsions
• Coma
• Urinary system reaction
Raise your hand if you agree BC should be tested more thoroughly. After all,
we are injecting our children with this.


Vaccine Ingredient: Glutaraldehyde

Glutaraldehyde is an organic compound that is used to disinfect medical and
dental equipment. In vaccines it is used as a chemical preservative. There
have been several studies done on Glutaraldehyde and it has been found
that exposure to it can cause:


• Asthma
• Allergic reactions (up to 10% of up people can be allergic to
Glutaraldehyde.)
• Induced respiratory issues

• Diarrhea

Sources: “Glutaraldehyde-induced and formaldehyde-induced allergic
contact dermatitis” SCOTT M. RAVIS, M.D., MATTHEW P. SHAFFER,
M.D., CHRISTY L. SHAFFER, M.D., SEENA DEHKHAGHANI,
M.D. and DONALD V. BELSITO, M.D.; “Glutaraldehyde-induced
asthma.” Quirce S, Gómez M, Bombín C, Sastre J. 1999 Oct;54(10):1121-
2.; Genetic toxicity and carcinogenicity studies of glutaraldehyde–a
review. Zeiger E, Gollapudi B, Spencer P. Mutat Res. 2005 Mar;589(2):136-
51; Divergent immunological responses following glutaraldehyde exposure.
Azadi S, Klink KJ, Meade BJ. Toxicol Appl Pharmacol. 2004 May
15;197(1):1-8.





Vaccine Ingredient: Cetyltrimethylammonium Bromide (CTMB)

Cetyltrimethylammonium Bromide is a cationic surfactant. It’s used for many
things, including acting as a buffer solution for extracting DNA. According to
it’s Safety Data Sheet we find out several things:


• CTMB is labeled as “Hazardous”
• It is a skin irritant
• It is a serious eye irritant
• It is hazardous if inhaled
• It is harmful if swallowed
• It may cause respiratory irritation
• It is dangerous to the environment
• It is very toxic to aquatic life with long lasting effects
• It is flammable
In almost all cases of any kind of contact with CTMB, it advises to contact a
medical professional and it advises that CTMB should never touch any part of
the human body. It also gives precautionary information and equipment to
use/wear during handling CTMB. Under section 8 Exposure
Controls/personal protection, it advises to:

Keep away from foodstuffs, beverages and feed.


Immediately remove all soiled and contaminated clothing


Wash hands before breaks and at the end of work.


Avoid contact with the eyes and skin.


This sounds like some pretty serious stuff, and millions of children and adults
are getting this injected into their bodies

In the “general information” for CTMB, it explains that “Symptoms of
poisoning may even occur after several hours” and the patient should be
observed for up to 48 hours after coming into contact with it. (How many
children have a reaction to a vaccine that isn’t immediate or even on the
first day? Hundreds. And yet if the reaction isn’t immediate, medical
professional dismiss the possibility of a vaccine reaction even faster.)









Vaccine Ingredients: Animal Organ Tissue and Animal Blood

Animal cell lines are used to culture the viruses in vaccines, so animal tissues
and impurities are included in the formulation that is injected. These tissues
are unusable and toxic to the body except for when their protein materials are
digested to form amino acids through normal food consumption. There is no
digestion process for injections.

Injections may also contain many types of animal viruses (see the Animal
Viruses section). Animals used include monkey (kidney), cow (heart), calf
(serum), chicken (embryo and egg), duck (egg), pig (blood), sheep (blood),
dog (kidney), horse (blood), rabbit (brain), guinea pig, etc.


Vaccine Ingredient: Large Foreign Proteins

In addition to the animal tissue impurities, there are large proteins that are
deliberately included, and used for such purposes as adjuvants (substances
that aggravate an immune response using their inherent toxicity). Egg album
and gelatin (or gelatine, obtained from selected pieces of calf and cattle
skins, de-mineralized cattle bones and pork skin) are in several vaccines.
Casein (milk protein) is in the triple antigen (DPT vaccine). When injected,
these normally harmless proteins are toxic to the body. Hence the immune
system “response”. The immune system is intentionally stressed by this
invasion to produce an unnatural sensitization to all the ingredients. The body
will become further sensitive to these substances in the future, rather than
becoming immune to them. So, the basic premise of vaccinations which the
public has been sold is false. This explains why bizarre allergies such as
lactose intolerance, egg, and nut allergies have suddenly become common in
recent history.

Vaccine Ingredient: Latex

This is included in the hepatitis B vaccine which is given routinely to health
workers. The high occurrence of the latex allergies among nurses is due to
their sensitization to latex through the large amounts of chemical rubber
which is injected into them. These vaccines produce a panicked immune
response. These nurses will suffer with this allergy permanently. Such allergic
reactions can be life -threatening.

This vaccine is now routinely given to newborn babies in many countries,
including Australia, and the United States.


Vaccine Ingredient: Animal Viruses

Some of these can be particularly alien to the human body. The most
frequently documented and publicised example is the monkey virus SV40.
The virus is harmless in monkeys, but it stimulates rare cancers when
injected into humans producing brain (tumors), bone (e.g. multiple myeloma),
lungs (mesothelioma), and lymphoid tissue (lymphoma). Monkey Virus SV40
has only appeared in people born in the last 20 years (The Journal of
Infectious Diseases, Sept. 1999), long after the manufacturer claimed to have
“cleaned up” the polio vaccines where it was found. Such cases include the
late Alexander Horwin, both of whose parents tested negative for SV40.

Therefore, recent cases cannot just be blamed on inheritance from parents
who received the vaccine (see www.ouralexander.org). This proves that
manufacturers are secretly including it again.



Vaccine Ingredient: Mycoplasma

These are microscopic organisms lacking rigid cell walls and considered to
be the smallest free-living organisms. Many are pathogenic, and one species
is the cause of mycoplasma pneumonia; which interestingly, is noted to occur
only “in children and young adults”, according to Mosby's Medical Dictionary.
This is not simply in vaccines by accident. It is deliberately added as an
adjuvant (to increase the immune system's allergic “response”) to the
vaccine. The ingredients must be either poisonous, or slightly biologically
infectious to trigger immune system responses, in other words.



Vaccine Ingredient: Foreign DNA

DNA is used from such organisms as animals, viruses, fungi, and bacteria. It
has been documented that injecting foreign DNA can cause it, or a portion of
it, to be incorporated into the recipient’s DNA. The horrendous long-term
multi- generational implications defy the imagination. Although, some people
might actually find it beneficial to have their grandchildren born with three
arms, or horns from the head. These possibilities may seem far-fetched, but
with the rate at which these type of ingredients are being incorporated into
vaccines, it is a matter of when they happen ― not if. Describing it as insane
is being too gracious.

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Issues
When your doctor won't report a vaccine reaction...
Vaccine Tracking
you should know that Federal law requires doctors or other health care professionals who give vaccines to:
Vaccine Mandates
REPORT ADVERSE EVENTS (hospitalizations, injuries, and deaths) occurring within 30 days of
Mercury/Thimerosal
vaccination, including convulsions, shock, paralysis and other serious events to the Vaccine Adverse Event
Emergency Powers Reporting System (VAERS). The doctor or other health care provider that administered the vaccination is not
supposed to make a judgment as to whether the adverse event that occurred following vaccination was
Homeland Security caused by the vaccine or not caused by the vaccine. The law says it is the duty of all vaccine administrators
to report the event to the federal government regardless of whether they believe the vaccine caused the
Medical Privacy/HIPAA event.
Conflicts of Interest RECORD ADVERSE EVENTS following vaccination in a person's permanent medical record.
KEEP A PERMANENT RECORD of the date, manufacturer's name and lot number of all vaccines given.
Your Rights and the Law
Exemptions PROVIDE INFORMATION on the vaccine benefits and risks BEFORE the vaccine is given either to the
individual who will receive the vaccine or the parent or guardian of that individual.
Harassment
If your doctor refuses to report a serious event which occurred following a vaccination given to you or your
Doctor Won't Report Reaction child within 30 days of vaccination to VAERS, you may:
Injury Compensation Program REPORT IT YOURSELF by calling 1-800-822-7967 to receive a government Vaccine Adverse
Events Report form, download the form by linking to http://www.fda.gov/cber/vaers/report.htm#form
Legal Help or submit it online at https://secure.vaers.org/VaersDataEntryintro.htm.

More information about VAERS can be found at http://www.vaers.org and
http://www.fda.gov/cber/vaers/vaers.htm.
Vaccines: A Closer Look
Vaccines and Diseases FILE A COMPLAINT OF PROFESSIONAL MISCONDUCT to the Texas State Board of Medical
Examiners.
Reactions
To make a complaint against a doctor please make your complaint in writing to:
Vaccination Decision Resources
Texas State Board of Medical Examiners
Texas Vaccine Rates Investigations Department MC-263
P.O. Box 2018

Animal Vaccines Austin, TX 78768-2018
Although it is not necessary to use a form to make a written complaint, they will send one to
Other Resources you. To receive a complaint form, please call 1-800-201-9353 and follow the automated
Books instructions. For more information see

http://www.tsbme.state.tx.us/complain/complain.htm
Websites
REPORT IT TO THE NATIONAL VACCINE INFORMATION CENTER, (NVIC), a national, non-profit,
educational organization founded in 1982 and dedicated to preventing vaccine injuries and deaths
through public education. By reporting to NVIC, they can better monitor the effectiveness of the
government's Vaccine Adverse Events Reporting System and gather important data on vaccine
reactions for analysis that the government and vaccine manufacturers do not do. Call (703)-938-
DPT3 and ask for an NVIC Vaccine Adverse Event Registry questionnaire to be sent to you. You
may also report a vaccine reaction to NVIC by accessing their web site at http://www.nvic.org


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incentive to come up with safer
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• Aluminum, a known neurotoxin, is
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