Vaccine aluminum linked to autism and other neurological
disorders.
The effects of poisons can be quick or extremely slow: building
gradually up creating low grade debilitation diseases like in chronic fatigue
syndrome or
devastating neurological
disorders
like MS, ALS, and Alzheimer's
disease. Aluminum is harmful to life. Aluminum is a
protoplasmic poison and a deadly, persistent neurotoxin. Aluminum is a known
toxin that can cause encephalitis, bone disease and anemia in susceptible
people. Autopsy reports on Alzheimer's patients found 70% more aluminum in the
brain. Though aluminum is less toxic than mercury, arsenic,
lead or cadmium, it is a persistent poison that increases the toxicity of other
heavy metals. Though neurodegenerative disorders have several pathways in their
creation but nothing will burn up a neuron faster than mercury. This is also
the case for aluminum hydroxide, just to a lesser extent. Vancouver
neuroscientist Dr. Chris Shaw just finished his research that shows a link
between the aluminum hydroxide used in vaccines, and symptoms associated with
Parkinson's, amyotrophic lateral sclerosis (ALS, or
Lou Gehrig's disease), and
Alzheimer's.[
i
]
(1-6)
80
percent of people tested have excessively high aluminum levels
,
a disturbing statistic, given
that metal toxicities are associated
with a wide range of chronic disease conditions.
(neurological, immune, and
mood disorders)
5
Scientific Findings Explain Link Between Vaccines and Autism
1. There is a permanent immune
system activation in the brains of people with autism.
2. Aluminum adjuvant is highly
neurotoxic and causes immune activation.
3. The immune activation that
triggers autism can happen in utero or after a child is born, while its brain
is still developing.
4. Hepatitis B vaccine-induced
IL-6 in postnatal rats.
5. Several analyses found high
levels of aluminum in the brains of people with autism.
Dr. Shaw found in animal studies that aluminum hydroxide shows
statistically significant increases in anxiety (38 percent); memory deficits
(41 times the errors as in the sample group); and an allergic skin reaction (20
percent). Tissue samples after the mice were "sacrificed" showed
neurological cells were dying. Inside the mice's brains, in a part that
controls movement, 35 percent of the cells were destroying themselves.
Neuroscience studies have clearly shown that sequential systemic
immune stimulation can activate the brain's immune system, microglia, and
astrocytes, and that with initial immune stimulation, there occurs CNS
microglial priming. Children are exposed to such sequential immune stimulation
via a growing number of environmental excitotoxins, vaccines, and persistent
viral infections. We demonstrate that fluoride and aluminum (Al3+) can
exacerbate the pathological problems by worsening
excitotoxicity
and inflammation. While Al3+
appears among the key suspicious factors of ASD, fluoride is rarely recognized
as a causative culprit. A long-term burden of these ubiquitous toxins has
several health effects with a striking resemblance to the symptoms of ASD. In
addition, their synergistic action in molecules of
aluminofluoride
complexes can affect cell signaling, neurodevelopment, and CNS functions at
several times lower concentrations than either Al3+ or fluoride acting alone
. (4-6)
Baby
Who Died 34 Hours After Vaccines Had Toxic Level of Aluminum in His Blood,
Report Confirms
The parents of 62-day-old Sawyer learned their baby’s blood
contained 95 micrograms per liter of aluminum, a level that would be neurotoxic
for adults. The toxicologist who read Sawyer’s report said the aluminum and
antigen levels in the blood were due to the vaccines.
VACCINE INDUCED AUTOIMMUNITY
Yehuda
Shoenfeld
et
al
,
Vaccines, adjuvants and
autoimmunity
.
Pharmacol
Research.
2015
Oct;100:190
-209.
vaccines can trigger autoimmunity
.
autoimmune
diseases that may occur following vaccinations include arthritis, lupus
(systemic lupus erythematosus, SLE) diabetes mellitus, thrombocytopenia,
vasculitis,
dermatomyosiositis
, Guillain-Barre
syndrome and demyelinating disorders
.
Almost all types of vaccines have been reported to be associated with the onset
of ASIA.” Autoimmune/inflammatory Syndrome Induced by Adjuvants (also known as
Shoenfeld's
syndrome)
A
summary of peer-reviewed scientific literature on
aluminum reproductive toxicity
by
Robert A. Yokel, Ph.D.
,
published in Critical Reviews in Toxicology.
The
review found aluminum exposure can lead to adverse reproductive outcomes
in
male and female mammals.
Vaccines show sinister side
By
Pieta Woolley
March
23, 2006
If two dozen
once-jittery mice at UBC are telling the truth postmortem, the world's
governments may soon be facing one hell of a lawsuit. New, so-far-unpublished
research led by Vancouver neuroscientist Chris Shaw shows a link between the
aluminum hydroxide used in vaccines, and symptoms associated with Parkinson's,
amyotrophic lateral sclerosis (ALS, or Lou Gehrig's disease), and
Alzheimer's.
Shaw is
most surprised that the research for his paper hadn't been done before. For 80
years, doctors have injected patients with aluminum hydroxide, he said, an
adjuvant that stimulates immune response.
"This
is suspicious," he told the Georgia Straight in a phone interview from his
lab near Heather Street and West 12th Avenue. "Either this
[link] is known by industry and it was never made public, or industry was never
made to do these studies by Health Canada. I'm not sure which is
scarier."
Similar adjuvants are
used in the following vaccines, according to Shaw's paper: hepatitis A and B,
and the
Pentacel
cocktail, which vaccinates
against diphtheria, pertussis, tetanus, polio, and a type of meningitis.
To test
the link theory, Shaw and his four-scientist team from UBC
and Louisiana State University injected mice with the
anthrax vaccine developed for the first Gulf War. Because Gulf War Syndrome
looks a lot like ALS, Shaw explained, the neuroscientists had a chance to
isolate a possible cause. All deployed troops were vaccinated with an aluminum
hydroxide compound. Vaccinated troops who were not deployed to the Gulf
developed similar symptoms at a similar rate, according to Shaw.
After 20
weeks studying the mice, the team found statistically significant increases in
anxiety (38 percent); memory deficits (41 times the errors as in the sample
group); and an allergic skin reaction (20 percent). Tissue samples after the
mice were "sacrificed" showed neurological cells were dying. Inside
the mice's brains, in a part that controls movement, 35 percent of the cells
were destroying themselves.
No
one in my lab wants to get vaccinated. This
totally creeped us out. We weren't out there to poke holes in
vaccines. But
all of a sudden
, oh my God-we've got
neuron
death! Dr.
Chris Shaw
Aluminum inhibits Na-K-ATPase and hexokinase enzymes
into the brain
. It blocks the electrical discharge of nerve cells, which reduces
nervous system activity.
Effect of Chronic Exposure to
Aluminium
on Isoform Expression
and Activity of Rat (Na
+
/K
+
)ATPase
,
Virgília
S. Silva, Ana I. Duarte, A.
Cristina Rego, Catarina R. Oliveira and Paula P. Gonçalves
Toxicological
Sciences 2005 88(2):485-494
"Our studies...
provide evidence that mercury, heavy metals and the vaccine preservative
thimerosal potently interfere with [methionine synthase] activation and
impair folate-dependent methylation. In vitro, mercury and
thimerosal in levels found several days after vaccination inhibit
methioninesynthetase
(MS) by 50%. Normal function
of MS is crucial in biochemical steps necessary for brain development,
attention and production of glutathione, an
important antioxidative and detoxifying agent. Repetitive doses of
thimerosal
leads
to neurobehavioral deteriorations in
autoimmune susceptible mice, increased oxidative stress and decreased
intracellular levels of glutathione in vitro.
Subsequent to
vaccination, autistic children have significantly decreased level of reduced
glutathione. Since each of these agents has been linked to developmental
disorders, our findings suggest that impaired methylation, particularly
impaired DNA methylation in response to growth factors, may be
an important molecular mechanism leading to developmental
disorders."
Activation of methionine synthase by insulin-like
growth factor-1 and dopamine: a target for neurodevelopmental toxins
and thimerosal. Waly M,
Olteanu
H, Banerjee R, Choi SW, Mason JB, Parker
BS, Sukumar S, Shim S, Sharma A,
Benzecry
JM, Power-
Charnitsky
VA,
Deth
RC. Mol Psychiatry. 2004
Apr;9(4):358-70
(these are also factors in autoimmune autism causation, Singh
et al)
According
to Dr. Russell Blaylock, "Removal of thimerosal, even if complete, will
not solve the problem of autism. It will help
tremendously,
but
will not stop the epidemic of autism. Though mercury, even in sub
toxic doses has been shown to strongly activate microglia causing the
secretion of two powerful excitotoxins, glutamate
and quinolinic acid, in concentrations that are neurotoxic.
Aluminum has a similar mode of action, though less potent. When combined with
mercury, there is at least additive toxicity if not synergistic toxicity."
Dr Gregory Ellis agrees with Blaylock stating that "autism is upon us
because it's the outcome of the 50-year experiment of dousing every living
being with an overload of toxic substances, including vaccines."[ii]
Speaking of her autistic patients, Dr Stephanie Cave said,
"You would be amazed at the devastation in their chemistries when you get
down to the cellular level." She also said, "I think in later years we
are going to look
back at aluminum the way we are looking at
mercury now."[iii]
"Aluminum
salts are used as vaccine adjuvants based on their ability to
improve dendritic cell response to presented antigens. The aluminum
concentration of vaccines varies from 0.125 to 0.85 mg/dose, which would
produce concentrations of approximately 0.7 to 4.5
uM
,
if uniformly distributed in the body water of a seven kg infant," reported
Dr. M. Waly at Northeastern University, who found that at these low
concentrations cellular problems are created independently and in combination
with
mercury.[
iv]
Aluminum given to a healthy subject will bring on symptoms of
tremors, forgetfulness, disorientation, a very dry, or weeping eczema and skin
rashes, as well as other nerve and brain tissue
disorders. The symptoms listed of aluminum
poisoning go on endlessly.
5
Scientific Findings Explain Link Between Vaccines and Autism
The
trigger for autism and other neurodevelopmental disorders, according to
Handley, is immune system activation that can alter the developing brain when
the activation occurs either in a pregnant mother or a young child.
This
happens because the neurotoxic aluminum in
vaccines
travels easily to the brain. There, it can
cause
inflammation
in vulnerable people by triggering the
production of a key
cytokine
-- interleukin 6 or
IL-6
--
a protein that affects the immune system.
IL-6 has been linked to autism
.
Handley,
author of the best-selling book, "
How to End the Autism Epidemic
," co-founder of
the
Age of Autism
website
and father of a son with autism, draws heavily on the
Vaccine Papers
website,
which collects and analyzes relevant science, to outline the key scientific
findings that make this case.
299
Aluminum
in Brain Tissue in Autism
All
4 male donors had significantly higher concentrations of brain aluminum than
the single female donor. We recorded some of the highest values for brain
aluminium
content ever measured in healthy or diseased
tissues in these male ASD donors including values of 17.10, 18.57 and
22.11 ?g
/g dry wt. (Table 1). What discriminates these data
from other analyses of brain
aluminium
in other
diseases is the age of the ASD donors. Why, for example would a
15 year old
boy have such a high content of aluminum in their
brain tissues? There are no comparative data in the scientific literature, the
closest being similarly high data for a 42 year old male with familial
Alzheimer’s disease (
fAD
)
https://www.sciencedirect.com/science/article/pii/S0946672X17308763
==============
https://open.substack.com/pub/tdefender/p/scientific-findings-explain-link-vaccines-autism-health-agencies-ignore
(This article efficiently rounded out my knowledge on
Aluminium
risks in the childhood vaccination schedule)
https://childrenshealthdefense.org/defender/under-the-skin-aluminum-hpv-vaccines-injuries/
Must
See:
Under the Skin
: How Aluminum Compounds in HPV Vaccines Cause
Injuries
Merck
Clinical Trials for HPV Vaccine was Fraudulent and did not prove the Vaccine
Safe or Effective.
See:
Under
the Skin
: How Aluminum Compounds in HPV Vaccines Cause Injuries
A
new
extra-strong
aluminum compound,
amorphous aluminum
hydroxyphosphate
sulfate
(AAHS), was used in the
Gardasil vaccine for human papillomavirus (HPV) and caused serious harm to
many.
A
team of Danish doctors
collected
dozens of cases and sent a safety warning to the European Medicines Agency
(EMA).
According to
The
BMJ
, documentation from the Danish Medicines Agency shows discrepancies in
trial documents of two Gardasil prelicensure clinical trials, one in
2002, and one in 2003.
For
both trials, the EMA appears to have authorized potassium aluminum sulfate as
the adjuvant and not
AAHS
so the trial was not
relevant to the vaccine with AAHS/
In
addition, the 2002 trial participants were told the comparator was saline, even
though the comparator was AAHS in an expedient consisting of L-histidine,
polysorbate-80, sodium borate and sodium chloride. There was no clinical trial
that showed the Gardasil vaccine safe or effective. Trial clearly fraudulent.
The EMA said AAHS was introduced without any prelicensure safety evaluation.
According
to The BMJ, aluminum adjuvants are associated with numerous adverse effects,
including injection site pain and tenderness, persistent lumps,
granulomas
, contact
dermatitis, post-immunization headache,
macrophagic
myofasciitis
and autoimmune/inflammatory
syndrome
induced by adjuvants.
Ehgartner
said numerous indications
show aluminum agents cause lasting damage to the immune system of many
vaccinated children and
adults, and
can lead to
permanent
ases
.
Almos
all mod ern diseases
such as allergies, autoimmune diseases, developmental disorders or
immune-related tumors
are connected with
a
hyper-aggressive immune system,
Ehgartner
said: we
show that these additives have never been tested for safety.
Vaccine
Adjuvant
danger
- MF59 Squalene oils & M
Squalene molecules are not broken down nor
are they excreted from the body; they end up in tissues where toxic reactions
can occur.
when molecules of squalene are
injected into humans, even at concentrations as small as 10 to 20 parts per
billion, the oil can lead to self-destructive immune responses, such as
autoimmune
arthritis and lupus
.
More than two dozen peer-reviewed scientific papers
from ten different laboratories throughout the U.S., Europe, Asia, and
Australia have been published documenting the development of autoimmune disease
in animals subjected to squalene-based adjuvants.
A recent study (December 2005)
discovered that Tween80 can cause anaphylaxis. MF59 is capable of accelerated
activation of the immune system, particularly the innate (in borne) or
cell-mediated immune system. Once the immune reaction is “turned on” there is no
available “switch” to turn it off. MF59 induces the expression (activation) of
at
least 891 genes
. It is the
most potent activator
of all adjuvants tested so far. The long-term
results of this activation are unknown and most likely will not be known.
MF
59 was not tested to see if it induces hypersensitivity or if it increases the
risk of anaphylaxis, allergies, or even cancer
.
Lead increases the toxicity of mercury
by a
hundred fold
, so does aluminum.
Dr.
Boyd Haley reported from his laboratory experiments that "Aluminum is not nearly
as toxic to neurons in culture as is thimerosal." At
the University of
Kentucky
he did
experiments to determine if aluminum would increase the toxicity of very low
levels of thimerosal. "The results were unequivocal: The presence of
aluminum dramatically increased the rate of neuronal death caused by
thimerosal. Therefore, the aluminum and thimerosal combination found
in vaccines produces a toxic mixture that cannot be compared to situations
where thimerosal alone was the toxic exposure."[v]
Mercury and aluminum not
only are directly toxic to brain cells but also over stimulate the brain's
immune system.
Dr. Russel Blaylock
According to Doctor Hugh
Fundenburg
if
an individual receives too many consecutive flu shots his/her chance of
developing Alzheimer's Disease is 10 times greater than if they had one, two or
no
shots.[
vi] When asked why, Dr.
Fudenberg
stated that it is due to the mercury and
aluminum buildup that are in many flu shots and in many other childhood
vaccines. The gradual mercury and aluminum buildup in the brain causes eventual
cognitive dysfunction.
Symptoms and Diseases of
Aluminum: Flatulence, headaches, dry skin, weak and aching muscles, senility,
spleen pain, stomach pain, liver dysfunction, kidney dysfunction, neuromuscular
disorders,
osteomalacia
, colitis, anemia,
Alzheimer's disease, amyotrophic lateral
sclerosis, hemolysis, leukocytosis, porphyria, heartburn, memory
loss, numbness, paralysis, Parkinson's disease, excessive perspiration, leg
twitching, cavities, colds, behavioral problems, constipation
The
kidneys eliminate Aluminum from the body and so people with renal
problems are at risk of Aluminum toxicity. All infants have
reduced renal function and may not be able to effectively excrete excessive
Aluminum. Kidney function is low at birth and reaches adult level by 1-2 years
of age. The presence of Aluminum in a vaccine can cause small nodules to
develop under the skin of some babies. These nodules are usually transient in
nature and disappear spontaneously after a
few weeks
.
In rare cases extreme hypersensitivity to Aluminum results in persistent
nodules.
----------------------------------------------------------------------------------
T
his review
(1)
describe
s
two mechanism
s
linking
aluminum to neurodegenerative processes and neurological dysfunction—systemic
activation of CNS mi- croglia and immunoexcitotoxicity. T
hese effects will amplify immunoexcitotoxic damage. In the immature and
developing brain, immunoexci- totoxicity
can
lead to a
number of neurodevelopmental conditions, such as autism spectrum disorders and
seizures. In the mature, and especially the aging brain, these mechanisms can
lead to progressive neurodegeneration, as seen with AD, PD and ALS
. (Dr. Russell
Blaylock)
Chronic brain inflammation
(2)
is known to enhance the sensitivity of glutamate receptors and interfere
with glutamate removal from the extraneuronal space, where it can trigger
excitotoxicity over a prolonged period. Neuroscience studies have clearly shown
that sequential systemic immune stimulation can activate the brain's immune
system, microglia, and astrocytes, and that with initial immune stimulation,
there occurs CNS microglial priming. Children are exposed to such sequential
immune stimulation via a growing number of environmental excitotoxins,
vaccines, and persistent viral infections. We demonstrate that fluoride and
aluminum (Al
3+
) can exacerbate the pathological
problems by worsening excitotoxicity and inflammation. While Al
3+
appears among the key suspicious factors of ASD, fluoride is
rarely recognized as a causative culprit. A long-term burden of these
ubiquitous toxins has several health effects with a striking resemblance to the
symptoms of ASD. In addition, their synergistic action in molecules of
aluminofluoride complexes can affect cell signaling, neurodevelopment, and CNS
functions at several times lower concentrations than either Al
3+
or fluoride acting alone.
(See references)
Chinese students receive treatment
at a hospital in
Lingbi
County, East
China's Anhui Province
, March 23, 2006.
More than 30 students
falls
ill
after measles vaccination at a primary school in the county, according to the
website of the Xinhua News Agency. [vii]
More than
3,000 children aged 1-14 in
Lingbi's
Xiangyang Township
were vaccinated on March 14,
2006
by the
county Center for Disease Prevention and Control in China. The township
hospital reported to the county government that 32 students developed steady
high fever after vaccination. But a reporter sent by a newspaper to schools
in Xiangyang found the figure was at least 150. Treatment continued
for the victims, all primary school students, whose fevers were as high as 41
degrees Celsius. (105.8 degrees
Farenheit
) More
and more we hear of such vaccine reactions and sometimes kids do die. The
medical authorities pretend there is nothing wrong with vaccines and act
surprised when kids get hurt. Most vaccines in the third world contain
thimerosal (mercury) and aluminum hydroxide.
Most
-- if not all -- chronic infectious diseases are not caused by a failure of the
immune
system, but
are a conscious adaptation of the
immune system to an otherwise lethal heavy metal
environment.
Dr.
Klinghardt
***************************************************************************************
The
synergism of toxic metals is well known to everyone except doctors and dentists
who do not want to know about this subject for it endangers their very way of
life and professional practice, not to speak about their
self-images.
With so much use of poison in the world one could easily come to
think that some groups of people are
actually trying
to poison the human race. And though mind boggling to think or believe this, we
find this is the case. A careful examination shows that there are
many companies and people who are in for fantastic profit and power and
collectively we could call this pharmaceutical terrorism, medical
insanity,
and genocide all rolled into one.
In
reality there
are no words that can truly describe the agony of being
that is created, the death and destruction and the personal hells on earth that
millions, even billions of people are being forced to live through.
What sort of consciousness does
it take to continue deliberately poisoning ourselves and our
families? What sort of consciousness does it take to
manufacture these poisons and sell them? And what kind
of consciousness lives with the illusion that it's safe to use
them in our medicines, dental fillings, and vaccines?
Some
people make a big fuss about which poison to protest and get the government to
stop using. When it comes to drugs and vaccines it is best to stay away from
poisons that hurt our kids. Almost ninety percent of the public support the
poisoning of children, they let their pediatricians get away with
horrors against their children. The medical establishment has led the
general public
to swallow hook line and sinker that the best
thing is to poison the kids.
Many
who are aware of the neurological damages done to children (autism epidemic)
via the mercury (thimerosal) in the vaccines do not realize as Dr. Blaylock
does that it's not enough to remove the mercury. Chemical rape is chemical
rape
and it really does not matter which one or how many of
them are involved in the dirty deed. It is not ok to chemically rape children
with mercury or aluminum or any of the other heavy metal. The FDA is the great
proponent of the use of poison, they ok the poisoning of the water
supply with fluoride and then go into psychotic fits when someone promotes
something that is not poisonous.
Aggressive pharmaceutical
marketing has resulted in almost 3 million children being prescribed strong,
adult anti-psychotic drugs.
Meanwhile
the FDA has nothing better to do than now attack the cherry
industry.[
viii]
The FDA recently told 29 cherry companies that by claiming their products could
prevent, treat or cure disease, they were in effect calling them drugs, which
are covered by the Food, Drug and Cosmetic Act. New drugs require FDA approval
and testing to confirm safety and effectiveness.
The
FDA admits that there are almost 1,000 safety and effectiveness studies that
have not been done for countless numbers of drugs permitted into the
marketplace by the
FDA, drugs that all contain poisons that create serious side
effects. It's a cruel joke that we have allowed the FDA to approve the safety
of poisonous drugs while we allow them to break the backs of companies
promoting healthy foods that prevent and even cure disease. Darth Vader and his
storm troopers have found a happy and well financed home at the FDA.
Mark
Sircus
Ac., OMD
Director International
Medical Veritas Association
http://www.worldpsychology.net
+55-83-3252-2195
www.skype.com
ID:
marksircus
The model by which adjuvants initiate
an immune response is that of Experimental Allergic Encephalomyelitis (EAE). To
date, EAE is recognized as the best available animal model of several
degenerative human diseases, like multiple sclerosis and
post-vaccinal encephalopathies. EAE
3
is generally thought to be an autoimmune response to myelin
basic protein (MBP). Oddly, MBP can also suppress EAE, and many
observations suggest that an independent immune response to so-called
"adjuvant" material is also necessary to EAE induction. Of course,
this is why adjuvants are used in vaccines, to dramatically increase
the likelihood of an immune response to the administered biological
material.
Thus, EAE may be a result of a pair of
interactive immune responses, one against MBP, and one against the
adjuvant. If so, the adjuvant should, like MBP, suppress EAE.
Root-Bernstein, et al. (1986) presented data from experiments on strain 13 guinea
pigs demonstrating EAE suppression by muramyl dipeptide, an active
component of complete Freund's adjuvant. In the past, adjuvants have
only been classified as immunopotentiators, not immunosuppressants.
Apparently, adjuvants are both. This study strengthens the argument
that adjuvants may be crucial to initiating an auto-immune response
leading to post-vaccine neurological symptoms.
Vaccine
Induced Demyelination
http://www.healing-arts.org/children/vaccines/vaccines-demyelination.htm#demyelination
Root-Bernstein RS,
Westall
FC:
Serotonin
binding sites.
II. Muramyl dipeptide binds to serotonin binding sites on myelin
basic protein, LHRH, and MSH-ACTH 4-10. Brain Res Bull 1990
Dec;25(6):827-41.
Abstract:
Department of
Physiology, Michigan State University, East
Lansing 48824.
Previously, we reported the existence of structurally similar serotonin binding
sites on myelin basic protein, LHRH, and MSH-ACTH 4-10. We now report that the
adjuvant peptide,
muramyldipeptide
(N-acetyl-muramyl-L-Ala-D-
isoGln
) also binds to these sites. This observation may
help to explain previous observations of serotonin-like activity
by muramyl peptides, including the promotion of slow-wave sleep and
fever induction. The observation may also provide an important link between the
immune system and the nervous system that may explain the
role
of muramyl dipeptide adjuvants in causing autoimmune
diseases to serotonin-regulated proteins and their receptors
, as well as
the alterations in serotonin levels that are often observed in autoimmune
diseases. The observation provides concrete evidence for a dual-antigen
hypothesis for the induction of autoimmune diseases by an adjuvant-peptide
complex. Application of such a mechanism for induction of autoimmunity may be
of importance in understanding a number
of postinfectious and postvaccinal neuropathies, and
suggests a possible etiology for autism, in which many patients have high blood
serotonin levels, autoimmune reactions to myelin basic protein, and antibodies
to serotonin binding sites. Finally, the observation suggests that
glycopeptides may act as neurotransmitters
Mercury
In
Vaccines
Was
Replaced
With Something Even MORE Toxic
The
short, eye-opening
eBook
linked below is titled
Aluminum in Vaccines -- a
Neurological Gamble
, by Neil Miller, director of the
Thinktwice
Global Vaccine Institute. It documents
the hazards associated with aluminum-laden vaccines. Children are receiving high
concentrations of aluminum in their shots. This well-documented neurotoxin may
be more dangerous than mercury.
Some vaccine proponents suggest that the failure of autism rates to decline
after removing mercury thimerosal from some vaccines shows vaccines were not
the primary cause of the greatly increased autism and ADHD rates of the last
decade.
However
some vaccines still contain mercury and Flu vaccines with high levels of
mercury have been added to the list of vaccines recommended for infants by authorities
as well as for pregnant women.
Also,
vaccines containing high concentrations of
neurotoxic
aluminum and other highly
neurotoxicadjuvants
,
including pesticides, were added to the child immunization schedule when
several vaccines containing mercury were removed. Two-month old babies now
receive 1,225 mcg of aluminum from their vaccines -- 50 times higher than
safety levels! Although the FDA, CDC and World Health Organization are aware of
the dangers, they expect parents to play Russian roulette with their children.
Sources:
·
Aluminum in Vaccines -- a Neurological
Gamble (PDF)
ADVERSE
EFFECTS OF ADJUVANTS IN VACCINES;
by
Viera
Scheibner
,
Ph.D.
www.whale.to/vaccine/adjuvants.html#ADJUVANTS,_PRESERVATIVES_AND_TISSUE_FIXATIVES_IN_VACCINES_
http://www.whale.to/v/quotes5.html
The article below nicely
summaries in bullet points the downsides of
Prevnar
Vaccine, including the use of
Prevnar
correlating with the increased, more
serious infections with E. coli, Salmonella, and Staphylococcus.
Prevnar: Is It Worth the Risk?
By F. Edward
Yazbak
,
MD, FAAP
http://www.jabs.org.uk/articles-by-fedward-yazbak.html
References:
(1)
Aluminum Induced Immunoexcitotoxicity in Neurodevelopmental and
Neurodegenerative Disorders
,
Current Inorganic Chemistry,
2012,
2,
000-000 1
,
Russell L.
Blaylock*
,
http://www.danmurphydc.com/wordpress/wp-content/uploads/2013/05/AR-04-14-blaylock-Aluminimum.pdf
&
http://www.chemtrailsaustralia.com/uploads/3/4/2/1/3421517/aluminum-blaylock.pdf
(2)
Immunoexcitotoxicity
as the central mechanism of
etiopathology and treatment of autism spectrum disorders: A possible role of
fluoride and aluminum;
Surg Neurol Int
. 2018; 9: 74.
Anna
Strunecka
,
Russell L. Blaylock, et al;
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909100/
Chronic brain inflammation
(2)
is
known to enhance the sensitivity of glutamate receptors and interfere with
glutamate removal from the extraneuronal space, where it can trigger
excitotoxicity over a prolonged period. Neuroscience studies have clearly shown
that sequential systemic immune stimulation can activate the brain's immune
system, microglia, and astrocytes, and that with initial immune stimulation,
there occurs CNS microglial priming. Children are exposed to such sequential
immune stimulation via a growing number of environmental excitotoxins,
vaccines, and persistent viral infections. We demonstrate that fluoride and
aluminum (Al
3+
) can exacerbate the
pathological problems by worsening excitotoxicity and inflammation. While Al
3+
appears among the key suspicious factors of ASD,
fluoride is rarely recognized as a causative culprit. A long-term burden of
these ubiquitous toxins has several health effects with a striking resemblance
to the symptoms of ASD. In addition, their synergistic action in molecules of
aluminofluoride complexes can affect cell signaling, neurodevelopment, and CNS
functions at several times lower concentrations than either Al
3+
or fluoride acting alone.
(4)
Fluoride,
aluminum, and
aluminofluoride
complexes in
pathogenesis of the autism spectrum disorders: A possible role of
immunoexcitotoxicity
.
Anna
Strunecka
,
Russell L. Blaylock
,1,*
Jiri Patocka
,2 and
Otakar
Strunecky
3 2016
(5)
Aluminofluoride
Complex
: Phosphate Analogues and a Hidden
Hazard for Living Organisms
Anna
Strunecka
,
Russell L. Blaylock
et al
(6)
Immunoexcitotoxicity
as the central
mechanism of cause and treatment of
autism
spectrum disorders
:
A role of aluminum and fluoride
. 2016
Anna
Strunecka
,
Russell L. Blaylock
,1,*
Jiri Patocka
,2 and
Otakar
Strunecky
3
.