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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/
Ricordo che,
molta importanza hanno anche i cibi assunti non
adatti al gruppo sanguigno del soggetto.
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
IV.
DETECTION OF MERCURY IN AUTISTIC CHILDREN
In
the past, hair, urine, or blood tests from autistic subjects have mostly
found lead rather than mercury (Wecker et al, 1985), but this is likely
due (i) to lead’s pervasiveness in our environment, coupled with
autistic children’s pica tendencies and general inability to detoxify any
heavy metal (LaCamera and LaCamera, 1987; Edelson & Cantor, 1998);
(ii) to the difficulty in detecting Hg, especially in older children
exposed early in life, since remaining mercury is sequestered in tissue;
and (iii) to the greater affinity of standard chelators used in
challenge tests (e.g., DMSA) for lead over mercury, making lead more
readily detectable in such exams (Frackelton and Christenson, 1998).
More
recently, a number of parents of younger autistic children, in whom
mercury is more likely to be detectable, have reported higher than
expected levels of mercury in hair, blood, and urine samples.
Cases studies are listed below, and more are in the process of
documentation. Several parents have also noted improved function after
chelation.
The
Case Studies
We
are providing data from several retrospective case studies of autistic
children with associated tissue mercury burdens.
In each case we have tried to identify potential sources of
exposure, although we have notbeen able to identify the exact amounts in
some cases due to inadequate documentation.
This information does not purport to be a rigid scientific study,
but rather an initial effort to demonstrate that there may be a problem
with mercury toxicity in children with autism.
Our primary objective is to show that considerable amounts of
mercury are found in the bodies of some autistic children.
The data we present were derived from many sources: hair, urine
and blood. Some of
the samples were baseline and others were obtained utilizing a
provocative agent, either DMPS or DMSA.
Typically a single dose of DMPS will provoke more mercury from
the tissue than a single oral dose of DMSA.
Excretion levels will also vary depending on the amount of DMPS
or DMSA given. There are
also variations among these factors in the case studies.
Identifier:
0001SM Sex: M
Age: 5
DOB: 4-25-94
Prenatal
and Postnatal History:
Premature contractions, which required bedrest during the 2nd and 3rd
trimesters.
Scheduled
C-section at term with good apgars. Birth weight 8 lbs. 3 oz. Vomiting milk based formula, which
subsided with a switch to soy formula at 2 months.
Developmental
Landmarks:
Completely normal development, meeting all developmental milestones until
20 months of age. Speech present with two word phrases.
Regression
and Symptoms:
At 20 months an unexplained loss of speech and eye contact (lateral
gaze). He began lining up
trains, developed preservations, and showed a marked decrease in
attention. Diagnosed autistic
at 26 months of age.
Formal
psychological evaluation at 30 months found expressive speech at 14-16
months, cognitive at 12-18 months, fine motor at 18 months, and play
skills at 12 months. He was
described as withdrawn with alternating inattention or repetitive
manipulation of objects.
Exposure
Sources:
He received multiple vaccines with thimerosal preservatives his first
year, including influenza
vaccine.
The documented exposure the first year
was 136.5mcg mercury. Mother
with 1 amalgam filling and minimal dietary exposure. Child with no dietary
exposure the first year of life. Families
estimated consumption of seafood 3 times monthly.
Mercury
Levels:
Hair mercury 2.6 mcg with a norm reference of less than 2mcg.
DMPS provacation (3mg per kg. IV) 7-7-99 resulted in 87 mcg mercury
per g urinary creatine. Intermittent treatment with oral DMSA continued
for 2 months with normalization of hair mercury levels.
Response
to Treatment:
Parents claim significant improvement in speech and behavior, also
documented on neuropsychological evaluation on 1-14 and 1-21-00.
“His ability to use language for social purposes has clearly
increased and he could maintain exchanges for several turns without
excessive difficulty. He has
improved in his ability to initiate interactions and invitation to other
children to play. Academic function at or above grade level.
Impressive and highly encouraging rate of progress.”
Identifier:
0002CM Sex:
M Age:
5 DOB:
12-1-94
Prenatal
and Postnatal History:
Unremarkable prenatal course.
Birth weight 8lbs.8oz.
Maintained
above the 95th percentile for height and weight the first year of life.
Developmental
Landmarks:
All early developmental landmarks - crawling, walking, and talking -
were obtained on schedule.
Regression
and Symptoms:
Child went from age appropriate to severe autistic regression
between 18 to 20 months.
He lost speech, eye contact and became inattentive and withdrawn.
Symptoms at 3 years include extreme thirst, echolalia, toe walking, high
pain threshold, sleep disturbances, hyperactivity and obsessive
behaviors.
Exposure
Sources:
No maternal amalgam history and minimal dietary exposure.
He received all recommended vaccines, although without
manufacturer data we are unable to calculate total exposure at this
time. Known exposure from hepatitis B vaccine, 37.5 mcg mercury.
Mercury
Levels:
Hair mercury was 2.21ppm at 3 years and 3 months of age with a
lab reference
of 0-1.5ppm.
DMPS provocation utilizing 3 mg. DMPS/kg given IV revealed:
46
micrograms of mercury / g creatine on 12-18-98
86
micrograms of mercury / g creatine on 3-25-99
46
micrograms of mercury / g creatine on 7-27-99
36
micrograms of mercury / g creatine on 9-30-99
Normal
reference for urinary mercury 0-3 micrograms / g creatine.
Between
DMPS infusions the child received DMSA 100 mg. orally two days a week,
with glutathione 75 mg. twice daily, glycine 900 mg. on day prior to
DMSA and glycine 900 mg. on DMSA treatment days.
Response
to treatment:
On 3-22-00 the parents reported marked behavioral improvement,
particularly over the past two months.
He now responds to his name and follows instructions.
He has developed original speech without echolalia, and obsessive
behaviors have declined.
Identifier:
0003HC Sex:
M
Age: 3yr.
11mo. DOB: 4-11-96
Prenatal
and Postnatal History:
Prenatal history was unremarkable.
Infant was thought to be 4 weeks premature, although birth weight
was that of a term infant at 8lbs. 6oz.
He developed jaundice shortly after birth and was treated with
phototherapy. He was
briefly given antibiotics for a suspected infection the first 3 days of
life.
Developmental
Landmarks:
Parents report that his development was normal until 12 months.
He was crawling but did not begin to walk until 18 months of age
with the support of a walker.
Regression
and Symptoms:
Some concerns at 13 months, marked regression at 16 months.
Six to seven spoken words in use at 12 months were entirely lost.
Vacant stares predominated and he began biting his hands.
Officially diagnosed autistic at 2 1/2 years
of
age.
Exposure
Sources:
Mother had 8 amalgams. He also received exposure via vaccine, but total dose is not
available at this time
Mercury
Levels:
Hair mercury at 2 years 7 months was below detection limits.
DMSA provacative protocol with 10 mg per kg per dose three times
daily for three days with 24 hr urine screen for heavy metals day 2
revealed:
3.2
micrograms of mercury / g creatine on 6-21-99
28
micrograms of mercury / g creatine on 9-13-99
13
micrograms of mercury / g creatine
on 10-12-99
Normal
lab reference 0-3 mcg Hg per g creatine.
Response
to treatment: Parents
feel certain that DMSA chelation has resulted in improvement in their
son.
They
noticed almost immediate improvement during the three days of treatment
along with dramatic improvement the past six months.
He is “much more with it and curious about his world”.
Although he is still not talking, he is having frequent
vocalizations.
He just started running for the first time 6 weeks ago.
Identifier:
0004WR Sex: M
Age: 6 DOB: 2-2-94
Prenatal
and Postnatal History:
Prenatal history unremarkable with the exception of breech presentation.
C-section preformed and apgars were 9 and 10. Birth weight, 8lbs.
11oz. Normal postnatal
course.
Developmental
Landmarks:
He easily met and exceeded all early developmental landmarks and was
described as a pleasant, happy baby.
Regression
and symptoms:
Shortly after his first birthday he developed numerous infections and
was hospitalized for a respiratory illness.
He received antibiotics, steroids, and oxygen and was discharged
on day three. By 15 months
he had lost speech and interaction.
At 18 months he developed a very limited diet with bouts of
bloody, culture negative diarrhea.
Officially diagnosed autistic at 5 yrs, although he had been
receiving services for autism from the school system since age 3.
Exposure
sources:
This child received all early vaccines with thimerosal preservative.
At 2 months of age he received 62.5 mcg of mercury which
represented a 125 fold increase above EPA guidelines based on his
weight. This occurred again
at 4 months, 62.5 mcg mercury and 50 mcg mercury at 6 months, 11 months
12.5mcg mercury and at 18 months, 50 mcg mercury for a total of 237.5
mcg of mercury. Mother also reports 5 dental amalgams and minimal
dietary exposure. Child has never eaten fish or seafood.
Mercury
Levels:
Hair analysis from 20 months revealed 4.8 ppm mercury with a reference
range of 0-1ppm and aluminum 40.2 with a reference of 0-9ppm. Note this
sample was not sent for analysis until the child was already 5 1/2 years
at which time the mother became aware of his early mercury exposure from
vaccines. A subsequent analysis at 5 ½ years revealed normal
levels of mercury and elevated lead 1.14 ppm with a normal reference
0-0.5, aluminum 23.2, and antimony 0.017 with reference of 0-0.03 and
bismuth 0.19 with reference of 0-0.11.
Initial treatment with oral DMSA removed 17 mcg per g creatine
lead with reference 0-15 mcg per g creatine. Oralcyclic chelation was
continued for 5 cycles with lead again present at 15 mcg per g creatine
down to normal levels at the 5th cycle.
Response
to treatment:
Parents report marked improvement with each round of chelation.
The last two cycles were not as pronounced as the first 3 cycles
of treatment.
An increase in spontaneous language and a general overall
increase in all areas of functioning were also noted.
Identifier:
0005ZH
Sex: M
Age: 10
DOB: 5-28-89
Prenatal
and Postnatal History:
Unremarkable pre- and postnatal course.
Term vaginal delivery.
Pitocin given for failure to progress. Birth weight 7 lbs. 14
oz., good apgars.
Developmental
Landmarks:
Mother reports he was a very alert and pleasant infant who easily
obtained all his early developmental landmarks with the exception of
crawling.
He progressed directly to walking at 8 ½ months.
He began to babble and had developed some speech the first year
of life, which did not progress.
Regression
and Symptoms:
Parents were concerned about his speech delay but attributed it to other
factors. He also developed a very picky diet with a preference for
starches.
He also would line up toys and repeat phrases but was not
officially diagnosed autistic until 5 years of age.
Exposure
Sources: Mother with
multiple dental amalgams. DPT vaccine known to have mercury 25 mcg per
dose at 2,4,and 6 months.
Child did eat fish sticks as a toddler but parents switched to
only farm raised fish.
Mercury
Levels:
A 24 hour heavy metal challenge at 9 years of age removed 67 mcg of
mercury.
Unfortunately, the parents were not able to financially afford
further treatment at that time.
Identifier:
0006MA
Sex: M
Age: 4 ½ yrs. DOB: 8-24-95
Prenatal
and Postnatal History:
Uncomplicated pregnancy, term vaginal delivery, apgars 9 and 10,
birth weight 7 lbs. 6 oz.
Quickly learned to breast feed, unremarkable postnatal history.
Developmental
Landmarks:
Easily met all early developmental milestones.
Described as being very social with good eye contact. He was
saying Mama, bye-bye, and babbling at 14 months.
Regression
and Symptoms:
According to the parents, at 16 to 17 months he began to slide
into his own world.
He stopped responding to his name and making eye contact.
He also lost language and social interactions.
Parents also report muted emotions.
Exposure
Sources:
This infant was exposed to 100 mcg mercury the first six months
of life via vaccines.
No dietary exposure from seafood or fish to the child.
Mother with 9 amalgam fillings and only occasional fish
consumption during pregnancy.
Mercury
Levels:
Hair analysis without mercury detection. Heavy metals challenge
urine 8.6 mcg / g / creatine with a norm reference of 0-2.5 mcg/ g /
creatine at 3 years 8 months of age. He is currently undergoing cyclic
chelation therapy with oral DMSA.
Response
To Treatment:
Parents report that his level of awareness, eye contact,
emotions, and receptive and
expressive language have all improved since starting the chelation
program.
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
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