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Autism
a Type of Mercury Poisoning  - 11
 
(English)
Relazione-Dossier del dott. M. Montinari su Autismo dai Vaccini
PROTOCOLLO DAN (dott. F. Verzella)
AUTISMO dai VACCINI - SENTENZA del TRIBUNALE
vedi qui: il PDF dello studio che indica la correlazione fra Autismo e Vaccini
INTERVISTA con il dott. William Shaw (USA)
Metalli tossici dei vaccini = Autismo vedi: PDF -  (dott. M. Proietti)
Sindrome della permeabilita' intestinale ed autismo
Il Thimerosal dei vaccini distrugge e/o altera la flora intestinale essendo una sostanza altamente tossica

MINERALOGRAMMA (test per conoscere il livello ed il tipo di intossicazioni da minerali e metalli tossici anche dei vaccini)
Il Thiomersal dei vaccini produce danni anche gravi
Metalli tossici
Danni al sistema enzimatico da Vaccini e metalli 
By Giusy Arcidiacono (CT) - arcidiaconogiusy@hotmail.com -
Perito Commerciale - chimico
Ecco il recente studio che ha coinvolto più di 17.000 bambini fino a 19 anni
Questo studio-indagine attualmente in corso è stato avviato dall’omeopata Andreas Bachmair.

La Verita' sullo studio del dott. Wakefield
Terapia Naturale per l'Autismo (Gaps)
AUTISMO e malattie varie dai Vaccini - Studi Pubblicati - PDF
 

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  - ABSTRACTBy 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.

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