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139 Research Papers Supporting Vaccine/Autism CausationGinger Taylor, MS
Mainstream research has found that vaccines and their ingredients can cause the underlying medical conditions that committed physicians and researchers are commonly finding in children who have been given an autism diagnosis. These conditions include gastrointestinal damage, immune system impairment, chronic infections, mitochondrial disorders, autoimmune conditions, neurological regression, glial cell activation, brain inflammation, damage to the blood–brain barrier, seizures, synaptic dysfunction, dendritic cell dysfunction, mercury poisoning, aluminum toxicity, gene activation and alteration, glutathione depletion, impaired methylation, oxidative stress, impaired thioredoxin regulation, mineral deficiencies, impairment of the opioid system, endocrine dysfunction, cellular apoptosis, and other disorders.
1.
Increased risk of developmental neurologic impairment after high exposure to thimerosalcontaining vaccine in first month of life. !ivision of "pidemiology and #urveillance, $accine #afety and !evelopment %ranch, &ational Immunization 'rogram, (enters for !isease (ontrol and 'revention. )***. Thomas M. $erstraeten, +obert !avis, !avid u, -rank !e#tefano %ackground (oncern has risen on the presence of the ethylmercury containing preservative thimerosal in vaccines. /e assessed the risk for neurologic and renal impairment associated with past exposure to thimerosalcontaining vaccine using automated data from the $accine #afety !ata link 0$#!1. $#! is a large linked database from four health maintenance organizations in /ashington, 2regon and (alifornia, containing immunization, medical visit and demographic data on over 344,444 infants born between 5*) and 5*6. Methods /e categorized the cumulative ethylmercury exposure from Thimerosalcontaining vaccines after one month of life and assessed the subse7uent risk of degenerative and developmental neurologic disorders and renal disorders beforethe age of six. /e applied proportional hazard models ad8usting for 9M2, year of birth, and gender, excluding premature babies.+esults /e identified :;< children with degenerative and =64: with developmental neurologic disorders, and =)4 with renal disorders. The relative risk 0++1 of developing a neurologic development disorder was ).; 0 *>? confidence intervals @(IA B).):.;1 when comparing the highest exposure group at ) month of age 0cumulative doseC :> ug1 to the unexposed group.
ithin thisgroup !e also "oun# an ele$ate# ris% "or the "ollo!ing #isor#ers& autism 'RR ()*, 9+ Cl - 1).31)+0
, non organic sleep disorders 0++ >.4, *>? (l B ).<)>.*D, and speech disorders 0++ :.), *>? 0)B).)3.41. -or the neurologic degenerative and renal disorders group we found no significantly increased risk or a decreased risk. (onclusion
This analysis suggests that high eposure to ethyl mercury "rom thimerosalcontaining $accines in the "irst month o" li"e increases the ris% o" su2seuent #e$elopment o" neurologic #e$elopment impairment
,
but not of neurologic degenerative or renal impairment. -urther confirmatory studies are needed.
2.
F Transl #ci = !2I )4.)>6<)GFT#.)444);<, Hpril :3, :4)6 Hnthony + Mawson, Hzad + %huiyan, %rian ! +ay, %inu Facob!epartment of "pidemiology and %iostatistics, #chool of 'ublic 9ealth, Fackson #tate Eniversity, Fackson, M# =*:)=, E#H&ational 9ome "ducation +esearch Institute, '2 %ox )=*=*, #alem, 2+ *6=4*, E#H Hbstract$accinations have prevented millions of infectious illnesses, hospitalizations and deaths among E.#. children, yet the longterm health outcomes of the vaccination schedule remain uncertain. #tudies have been recommended by the E.#. Institute of Medicine to address this 7uestion. This study aimed )1 to compare vaccinated and unvaccinated children on a broad range of health outcomes, and :1 to determine whether an association found between vaccination and neurodevelopmental disorders 0&!!1, if any, remained significant after ad8ustment for other measured factors. H crosssectional study of mothers of children educated at home was carried out in collaboration with homeschool organizations in four E.#. states -lorida, ouisiana, Mississippi and 2regon. Mothers were asked to complete an anonymous online 7uestionnaire ontheir < to ):yearold biological children with respect to pregnancyrelated factors, birth history, vaccinations, physiciandiagnosed illnesses, medications used, and health services. &!!, a derived diagnostic measure, was defined as having one or more of the following three closelyrelated diagnoses a learning disability, Httention !eficient 9yperactivity !isorder, and Hutism #pectrum !isorder. H convenience sample of <<< children was obtained, of which :<) 0=*?1 were unvaccinated. The vaccinated were less likely than the unvaccinated to have been diagnosed with chickenpox and pertussis, but more likely to have been diagnosed with pneumonia, otitis media, allergies and &!!. Hfter ad8ustment, vaccination, male gender, and preterm birth remained significantly associated with &!!. 9owever, in a final ad8usted model with interaction, vaccination but not preterm birth remained associated with &!!, while the interaction of preterm birth and vaccination was associated with a <.<fold increased odds of &!! 0*>? (I :.;, )>.>1.
4n conclusion, $accinate# homeschool chil#ren !ere "oun# to ha$e a higher rate o" allergies an# 566than un$accinate# homeschool chil#ren)
/hile vaccination remained significantly associated with &!! after controlling for other factors, preterm birth coupled with vaccination was associated with an apparent synergistic increase inthe odds of &!!. -urther research involving larger, independent samples and stronger research designs is needed to verify and understand these unexpected findings in order to optimize the impact of vaccines on childrenJs health."xerpts
K
566, a #eri$e# #iagnostic measure, !as #e"ine# as ha$ing one or more o" the "ollo!ing three closelyrelate# #iagnoses& a learning #isa2ility, Attention 6e"icient 7yperacti$ity 6isor#er, an# Autism Spectrum 6isor#er)
KK(hronic illness
Vaccinate# chil#ren !ere signi"icantly more li%ely than the un$accinate# to ha$e 2een #iagnose# !ith the "ollo!ing&
allergic rhinitis 0)4.3? vs. 4.3?, p L4.44) 2+ =4.), *>? (I 3.), :)*.=1, other allergies 0::.:? vs. <.*?, p L4.44) 2+ =.*, *>? (I :.=, <.<1, eczemaGatopic dermatitis 0*.>? vs. =.<?, p B 4.4=> 2+ :.*, *>? (I ).3, <.)1, a learning disability 0>.6? vs. ).:?, p B 4.44= 2+ >.:, *>? (I ).<, )6.31, H!9! 03.6? vs. ).4?, p B 4.4)= 2+ 3.:, *>? (I ).:, )3.>1,
AS6 '8)( $s) 1), p - )13: ;R 8)<, 9+ C4& 1)<, 18)+0
, any neurodevelopmental disorder 0i.e., learning disability, H!9! or H#!1 0)4.>? vs. =.)?, p L4.44) 2+ =.6, *>? (I ).6, 6.*1 and any chronic illness 033.4? vs. :>.4?, p L4.44) 2+ :.3, *>? (I ).6, =.=1.K
3.
:44:.allagher (M, oodman M#.F Toxicol "nviron 9ealth H. :4)46=0:31)<<>66. doi )4.)4;4G)>:;6=*3.:4)4.>)*=)6. HbstractEniversal hepatitis % vaccination was recommended for E.#. newborns in )**) however, safety findings are mixed. The association between hepatitis % vaccination of male neonates and parental report of autism diagnosis was determined. This crosssectional study used weighted probability samples obtained from &ational 9ealth Interview #urvey )**6:44: data sets. $accinationstatus was determined from the vaccination record. ogistic regression was usedto estimate the odds for autism diagnosis associated with neonatal hepatitis % vaccination among boys age =)6 years, born before )***, ad8usted for race, maternal education, and twoparent household.
=oys $accinate# as neonates ha# three"ol# greater o##s "or autism #iagnosis compare# to 2oys ne$er $accinate# or $accinate# a"ter the "irst month o" li"e)
&on9ispanic white boys were <3? less likely to have autism diagnosis relative to nonwhite boys. -indings suggest that E.#. male neonates vaccinated with the hepatitis % vaccineprior to )*** 0from vaccination record1 had a threefold higher risk for parental report of autism diagnosis compared to boys not vaccinated as neonates during that same time period. &onwhite boys bore a greater risk.