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Vaccinazioni per l’infanzia ed
autismo
Metalli tossici
dei vaccini = Autismo vedi: PDF - dott.
M. Proietti
Sentenza 2012 - Trib. Rimini su
Vaccini=Autismo
Commento NdR: sulla sentenza di Rimini: vaccini =
autismo
BENE ha
fatto il Giudice del Tribunale di Rimini (Italia) a
sentenziare in quel modo, perche' egli non si e'
lasciato influenzare dalle FALSITA' del Ministero della "salute" (che e'
stato da noi
informato sui Danni dei vaccini dal 1996 e
se ne sta zitto.....assieme a
tutti gli altri "enti"....) fino agli ordini
dei medici......tutti al servizio di
Big Pharma !
- vedi lo studio del dott.:
Wakefield.htm
In CINA dopo le campagne vaccinali esplode
l'Autismo ! - Maggio 2016
http://yournewswire.com/autism-rates-explode-in-asia-after-introducing-western-vaccines/
VERISSIMO, ma non solo l'autismo....ma una
innumerevole sequela di altre
malattie....
Autismo
e non solo dai Vaccini:
USA, Giugno 2013 - AUTISMO = 1 bambino
autistico su 26, non come era nel 2010, 1
su 80 ....
vedi QUI:
http://autismovaccini.com/2012/05/01/statistiche-per-lautismo-a-confronto-probabile-1-ogni-29-anziche-1-ogni-88/
I Tribunali anche USA, confermano tranquillamente che il
vaccino
MMR causa l'autismo. Austin (USA) - 27 Luglio 2013
Dopo decenni di appassionato dibattito, per i genitori che
probabilmente hanno perso i ripetuti ricorsi richiesti dalle
aziende farmaceutiche e governi, che i vaccini infatti causano
l'autismo.
Per i genitori interessati alla ricerca della verità, vale la
pena ricordare che le stesse persone che possiedono le aziende
farmaceutiche di tutto il mondo possono anche possedere agenzie
di stampa americane.
La Ricerca di informazioni prive di propaganda è stata fino ad
ora molto difficile.
Ma Whiteout Press non è qui per sostenere o contrastare i
vaccini. Siamo qui per portare i lettori la notizia che è il
tema e’ in black-out, cover-up e censurato dalle autorita’Sanitarie
e Governative.
Tratto da:
http://www.whiteoutpress.com/timeless/courts-quietly-confirm-mmr-vaccine-causes-autism/
La prova della FRODE del
CDC
per le cause dei
Vaccini
nell'Autismo
- CONFESSIONE di un alto dirigente
CDC, davanti al Congresso US
Gli esperti di
vaccini
del
CDC, hanno spesso
conflitti di
interesse
- 18/03/2010
CDC e
Conflitti di interesse - 1
+
CDC e Conflitti
di interesse - 2
+
CDC e Conflitti
di interesse - 3
+
Corruzione
+
Danni dei
Vaccini +
Contro Immunizzazione
CDC
conflitti di
interesse
anche per i vaccini +
anche per la FDA
http://healthimpactnews.com/2014/cdcs-purchase-of-4-billion-of-vaccines-a-conflict-of-interest-in-overseeing-vaccine-safety/
Davvero inquietante !
Questo medico il Dott.
Andrew Moulden è MORTO (probabilmente
assassinato) in modo inspiegabile nel
novembre 2013 al età di 49, subito dopo
aver pubblicato Le SUE RICERCHE che
DIMOSTRANO il DANNO CAUSATO dai VACCINI,
RICONOSCIBILI SOLO da un SEMPLICE ESAME
ESTERNO
http://vaccineimpact.com/2015/dr-andrew-moulden-learning-to-identify-vaccine-damage/
Parlamentari pagati dalle Lobbies ? -
Roma Ott. 2013
L'intervista a un assistente di un Senatore
che svelerebbe i traffici illeciti tra
parlamentari e
Lobbies.
Video dell'intervista:
http://www.video.mediaset.it/video/iene/puntata/390060/roma-parlamentari-pagati-dalle-lobbies.html
Informatore dei
CDC
CONFESSA la FRODE e le FALSIFICAZIONI sugli
studi della correlazione VACCINO=AUTISMO
AUTISM -
ABSTRACT-
By
Sallie
Bernard*,
Albert Enayati, B.S., Ch.E., M.S.M.E.
Heidi Roger, Teresa Binstock,
Lyn Redwood, R.N., M.S.N., C.R.N.P. -
Woody McGinnis, M.D. -
Contact:
sbernard@nac.net
Autism
is a neurodevelopmental syndrome characterized by impairments in social
relatedness, language, and communication, a need for routine and
sameness,abnormal movements, and sensory dysfunction.
Mercury is a toxic metal that can exist as a pure element or in a
variety of inorganic and organic forms and can cause immune, sensory,
neurological, motor, and other behavioral dysfunctions.
The
characteristics of autism and mercury poisoning, derived from a review
of medical literature, have been found, upon comparison, to be
strikingly similar. The characteristics of both disorders are summarized
in the following table and fully elucidated in the body of this
document. The parallels between the two diseases are so close that it
would be unreasonable to assume that the similarities occur by chance.
We
claim that autism is a form of mercury poisoning, based on similarities
of characteristics and on the known exposure to mercury of the majority
of US children. The exposure route is childhood vaccines, most of which
contain thimerosal, a preservative comprised of 50% ethylmercury by
weight. The amount of mercury a typical child under two years receives
from vaccinations equates to 237.5 micrograms, or 3.53 x 1017
molecules (353,000,000,000,000,000 molecules), most of which is not
excreted and goes directly to the brain. The amount is known to exceed
Federal safety standards, but is still considered a“low” level,such
that only a small percentage of exposed individuals will exhibit signs
of toxicity. Affected
individuals are those genetically prone to mercury sensitivity, which is
consistent with the observed high heritability rate of autism.
Furthermore, the timing of mercury exposure via vaccines
coincides with the emergence of autistic symptoms. Moreover, mercury has
been detected in urine, hair, and blood samples from autistic children,
and parental reports, though limited at this date, indicate significant
improvement in symptoms with administration of standard heavy metal
chelators. Thus, the four agreed-upon criteria used by clinicians to
diagnose mercury poisoning – i.e., observable symptoms, known exposure
at the time of symptom onset, detectable levels in biologic samples, and
improvement with chelation - have been met for autism.
The phenotypic
expression of mercury poisoning varies by a host of factors –
including type of mercury given, method of administration, rate and
level of dose, individual genotype, and age of patient – so that each
variation in factors has created in the past a slightly different
manifestation of the disease – Mad Hatter’s disease, Minamata
disease, and acrodynia, for example.
The pathology arising from the set of mercury-related variables
involved in autism – intermittent bolus doses of ethylmercury injected
into genetically susceptible infants and toddlers – has never been
reported before in medical literature. Thus we argue that autism
represents a unique form of mercury poisoning not heretofore described.
Our findings have widespread implications for the affected population of
autistic individuals, for other unexplained disorders with symptoms
similar to heavy metal intoxication, and for childhood vaccination
programs.
Summary
Comparison of Characteristics
of Autism &
Mercury Poisoning
|
Mercury
Poisoning |
Autism |
|
Psychiatric |
Social
deficits, shyness, social withdrawal |
Social
deficits, social withdrawal, shyness |
| Disturbances |
|
Depression,
mood swings; mask face
|
|
Depressive
traits, mood swings; flat affect |
|
Anxiety |
Anxiety |
|
Schizoid
tendencies, OCD traits |
Schizophrenic & OCD
traits; repetitiveness |
|
Lacks eye contact, hesitant to engage others |
Lack of eye contact, avoids conversation |
|
Irrational fears |
Irrational fears |
|
Irritability,
aggression, temper tantrums |
Irritability,
aggression, temper tantrums |
|
Impaired face recognition |
Impaired face recognition |
|
|
|
| Speech, |
Loss of speech, failure to develop speech |
Delayed
language, failure to develop speech |
| Language & |
Dysarthria; articulation problems |
Dysarthria; articulation problems |
| Hearing |
Speech comprehension deficits |
Speech comprehension deficits |
| Deficits |
Verbalizing & word retrieval problems |
Echolalia; word use & pragmatic errors |
|
Sound sensitivity |
Sound sensitivity |
|
Hearing
loss; deafness in very high doses |
Mild to profound hearing loss |
|
Poor performance on language IQ tests |
Poor performance on verbal IQ tests |
|
|
|
| Sensory |
Abnormal sensation in mouth & extremities |
Abnormal sensation in mouth & extremities |
| Abnormalities |
Sound sensitivity |
Sound sensitivity |
|
Abnormal touch sensations; touch aversion |
Abnormal touch sensations; touch aversion |
|
Vestibular abnormalities |
Vestibular abnormalities |
|
|
|
| Motor Disorders |
Involuntary jerking movements - arm flapping, ankle
jerks, myoclonal jerks, choreiform movements, circling, rocking |
Stereotyped movements - arm flapping, jumping,
circling, spinning, rocking; myoclonal jerks; choreiform movements |
|
Deficits in eye-hand coordination; limb apraxia;
intention tremors |
Poor eye-hand coordination; limb apraxia; problems
with intentional movements |
|
Gait
impairment; ataxia – from incoordination
& clumsiness to inability to walk, stand, or sit; loss of motor
control |
Abnormal gait and posture, clumsiness and
incoordination; difficulties sitting, lying, crawling, and walking |
|
Difficulty in chewing or swallowing |
|
Difficulty
chewing or swallowing
|
|
|
Unusual
postures |
Unusual
postures |
|
|
|
| Cognitive
Impairments |
Borderline
intelligence, mental retardation - some cases reversible |
Borderline
intelligence, mental retardation - sometimes "recovered" |
|
Poor
concentration, attention, response inhibition |
Poor
concentration, attention, shifting attention |
|
Uneven
performance on IQ subtests |
Uneven
performance on IQ subtests |
|
Verbal
IQ higher than performance IQ |
Verbal
IQ higher than performance IQ |
|
Poor
short term, verbal, & auditory memory |
Poor
short term, auditory & verbal memory |
|
Poor
visual and perceptual motor skills, impairment in simple reaction
time |
Poor
visual and perceptual motor skills, lower performance on timed tests |
|
Difficulty
carrying out complex commands |
Difficulty
carrying out multiple commands |
|
Alexia
(inability to comprehend the meaning of written words) |
Hyperlexia
(ability to decode words while lacking word
comprehension) |
|
Deficits
in understanding abstract ideas & symbolism; degeneration of
higher mental powers |
Deficits
in abstract thinking & symbolism, understanding other’s mental
states, sequencing, planning & organizing |
| Unusual |
Stereotyped
sniffing (rats) |
Stereotyped,
repetitive behaviors |
| Behaviors |
ADHD
traits |
ADHD
traits |
|
Agitation,
unprovoked crying, grimacing, staring spells |
Agitation,
unprovoked crying, grimacing, staring spells |
|
Sleep
difficulties |
Sleep
difficulties |
|
Eating
disorders, feeding problems |
Eating
disorders, feeding problems |
|
Self
injurious behavior, e.g. head banging |
Self
injurious behavior, e.g. head banging |
|
|
|
| Visual |
Poor
eye contact, impaired visual fixation |
Poor
eye contact, problems in joint attention |
| Impairments |
“Visual
impairments,” blindness, near-sightedness, decreased visual acuity |
“Visual
impairments”; inaccurate/slow saccades; decreased rod functioning |
|
Light
sensitivity, photophobia |
Over-sensitivity
to light |
|
Blurred
or hazy vision |
Blurred
vision |
|
Constricted
visual fields |
Not
described |
|
|
|
| Physical
Disturbances |
Increase
in cerebral palsy; hyper- or hypo-tonia; abnormal reflexes; decreased
muscle strength, especially upper body; incontinence; problems chewing,
swallowing, salivating |
Increase
in cerebral palsy; hyper- or hypotonia; decreased muscle strength,
especially upper body; incontinence; problems chewing and swallowing |
|
Rashes,
dermatitis/dry skin, itching; burning |
Rashes,
dermatitis, eczema, itching |
|
Autonomic
disturbance: excessive sweating, poor circulation, elevated heart
rate |
Autonomic
disturbance: unusual sweating, poor circulation, elevated heart rate |
|
|
|
| Gastro-intestinal |
Gastroenteritis,
diarrhea; abdominal pain, constipation, “colitis” |
Diarrhea,
constipation, gaseousness, abdominal discomfort, colitis |
| Disturbances |
Anorexia,
weight loss, nausea, poor appetite |
Anorexia;
feeding problems/vomiting |
|
Lesions
of ileum & colon; increases gut permeability |
Leaky
gut syndrome |
|
Inhibits
dipeptidyl peptidase IV, which cleaves casomorphin |
Inadequate
endopeptidase enzymes needed for breakdown of casein & gluten |
|
|
|
| Abnormal
Biochemistry |
Ties
up -SH groups; blocks sulfate transporter in intestines, kidneys |
Low
sulfate levels |
|
Has
special affinity for purines & pyrimidines |
Purine
& pyrimidine metabolism errors lead to autistic features |
|
Reduces
availability of glutathione, needed in cells & liver to detoxify heavy
metals |
Low
levels of glutathione; decreased ability of liver to detoxify heavy metals |
|
Causes
significant reduction in glutathione peroxidase and glutathione
reductase |
Abnormal
glutathione peroxidase activities in erythrocytes |
|
Disrupts
mitochondrial activities, especially in brain |
Mitochondrial
dysfunction, especially in brain |
|
|
|
| Immune
Dysfunction |
Sensitivity
due to allergic or autoimmune reactions; sensitive individuals more likely
to have allergies, asthma, autoimmune-like symptoms, especially
rheumatoid-like ones |
More
likely to have allergies and asthma; familial presence of autoimmune
diseases, especially rheumatoid arthritis; IgA deficiencies |
|
Can
produce an immune response in CNS |
On-going
immune response in CNS |
|
Causes
brain/MBP autoantibodies |
Brain/MBP
autoantibodies present |
|
Causes
overproduction of Th2 subset; kills/inhibits lymphocytes, T-cells, and
monocytes; decreases NK T-cell activity; induces or suppresses IFNg &
IL-2 |
Skewed
immune-cell subset in the Th2 direction; decreased responses to T-cell
mitogens; reduced NK T-cell function; increased IFNg & IL-12 |
| CNS
Structural Pathology |
Selectively
targets brain areas unable to detoxify or reduce Hg-induced oxidative
stress |
Specific
areas of brain pathology; many functions spared |
| |
Damage
to Purkinje and granular cells |
Damage
to Purkinje and granular cells |
| |
Accummulates
in amygdala and hippocampus |
Pathology
in amygdala and hippocampus |
| |
Causes
abnormal neuronal cytoarchitecture; disrupts neuronal migration & cell
division; reduces NCAMs |
Neuronal
disorganization; increased neuronal cell replication, increased glial
cells; depressed expression of NCAMs |
| |
Progressive
microcephaly |
Progressive
microcephaly and macrocephaly |
| |
Brain
stem defects in some cases |
Brain
stem defects in some cases |
| |
|
|
| Abnormalities
in Neuro-chemistry |
Prevents
presynaptic serotonin release & inhibits serotonin transport; causes
calcium disruptions |
Decreased
serotonin synthesis in children; abnormal calcium metabolism |
| |
Alters
dopamine systems; peroxidine deficiency in rats resembles mercurialism in
humans |
Possibly
high or low dopamine levels; positive response to peroxidine (lowers
dopamine levels) |
| |
Elevates
epinephrine & norepinephrine levels by blocking enzyme that degrades
epinephrine |
Elevated
norepinephrine and epinephrine |
| |
Elevates
glutamate |
Elevated
glutamate and aspartate |
| |
Leads
to cortical acetylcholine deficiency; increases muscarinic receptor
density in hippocampus & cerebellum |
Cortical
acetylcholine deficiency; reduced muscarinic receptor binding in
hippocampus |
| |
Causes
demyelating neuropathy |
Demyelation
in brain |
| |
|
|
| EEG
Abnormalities/ |
Causes
abnormal EEGs, epileptiform activity |
Abnormal
EEGs, epileptiform activity |
| Epilepsy |
Causes
seizures, convulsions |
Seizures;
epilepsy |
| |
Causes
subtle, low amplitude seizure activity |
Subtle,
low amplitude seizure activities |
| |
|
|
| Population |
Effects
more males than females |
Male:female
ratio estimated at 4:1 |
| Charact-eristics |
At
low doses, only affects those geneticially susceptible |
High
heritability - concordance for MZ twins is 90% |
| |
First
added to childhood vaccines in 1930s |
First
"discovered" among children born in 1930s |
| |
Exposure
levels steadily increased since 1930s with rate of vaccination, number of
vaccines |
Prevalence
of autism has steadily increased from 1 in 2000 (1940s) to 1 in 500
(1990s) |
| |
Exposure
occurs at 0 - 15 months; clinical silent stage means symptom emergence
delayed; symptoms emerge gradually, starting with movement & sensation |
Symptoms
emerge from 4 months to 2 years old; symptoms emerge gradually, starting
with movement & sensation |
vedi:
AUTISMO
+
Autism
REFERENCES
+
Autismo dai VACCINI
+
Autismo - La prova dei
Danni dei Vaccini
+
Bibliografia su Autismo dai vaccini +
Bibliografia
Danni dei vaccini +
Bibliografia danni
2 + Amish
senza autismo perche' NON vaccinano +
1.000 studi sui Danni dei Vaccini
Ricordo che,
molta importanza hanno anche i cibi assunti non
adatti al gruppo sanguigno del soggetto.
Continua in:
Pag.1 - Pag.2 -
Pag.3 - Pag.4 - Pag.5 - Pag.6 - Pag.7
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Pag.12
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