76 Scientific Studies Prove VACCINES CAUSE AUTISM

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DOCUMENTS ON THE ADVERSE EFFECTS OF THIMEROSAL (MERCURY, MERTHIOLATE, ETHYL MERCURY), DOCUMENTS SHOWING GASTROINTESTINAL ABNORMALITIES and DOCUMENTS SHOWING IMMUNE SYSTEM IRREGULARITIES IN AUTISTIC CHILDREN … (Many more exist - Jagannath)1) Bradstreet J, Geier DA, Kartzinel, JJ, Adams JB, Geier MR.A case control study of mercury burden in children with autistic spectrum disorders.J Am Phys Surg 2003; 8:76-9.2) The National Toxicology Program (NTP) within US Dept. of Health and Human Services, aninteragency program headquartered at the National Institutes of Health’s National Institute ofEnvironmental Health Sciences (NIEHS) on Thimerosal.They report: “Poison by ingestion, subcutaneous, intravenous and possibly other routes.â€3) Lowell JA, Burgess S, Shenoy S, Peters M,

Howard TK.Mercury poisoning associated with hepatitis-B immunoglobulin..Lancet 1996; 347:480.4) Baskin DS, Ngo H, Didenko VV.Thimerosal induces DNA breaks, caspase-3 activation, membrane damage, and cell death incultured human neurons and fibroblasts.Toxicol Sci 2003; 74:361-8.5) Heyworth MF, Truelove SC.Problems associated with the use of merthiolate as a preservative in anti-lymphocytic globulin.Toxicology 1979; 12:325-33.6) Forstrom L, Hannuksela M, Kousa M, et al.Merthiolate hypersensitivity and vaccination.Contact Dermatitis 1980; 6:241-5.7) Rohyans J, Walson PD, Wood GA, MacDonald WA.Mercury toxicity following merthiolate ear irrigations.J Pediatr 1984; 104:311-13.8 Kravchenko AT, Dzagurov SG, Chervonskaia GP.Evaluation of the toxic action of prophylactic and therapeutic preparations on cells cultures.Communication III. Revealing the toxic properties of medical biological

preparations from thedegree of cell damage in continuous cell line L132.Zh Mikrobiol Epidemiol Immunobiol 1983; 3:87-92.9) Cox NH, Forsyth A.Thimerosal allergy and vaccination reactions.Contact Dermatitis 1988; 18:229-33.10) Uchida T, Naito S, Kato H, Hatano I, Harashima A, Terada Y, Ohkawa T, Chino F, Eto K.Thimerosal induces toxic reaction in non-sensitized animals.Int Arch Allergy Immunol. 1994 Jul; 104(3): 296-301.11) Seal D, Ficker L, Wright P, Andrews V.The case against thimerosal.Lancet 1991; 338:315-6.12) The Material Safety Data Sheets (MSDS) for thimerosal indicate, “TOXICOLOGY: Poison.Experimental neoplastigen and teratogen. Harmful by inhalation and ingestion. May causereproductive damage. May be harmful through skin contact.â€13) Kiffe M, Christen P, Arni P.Characterization of cytotoxic and genotoxic effects of different compounds in CHO K5 cells withthe comet assay

(single-cell gel electrophoresis assay).Mutat Res. 2003 June 6; 537(2):151-68.14) Fagan DG, Pritchard JS, Clarkson TW, Greenwood MR.Organ mercury levels in infants with omphaloceles treated with organic mercurial antiseptic.Arch Dis Child. 1977 Dec; 52(12):962-4.15) Cinca I, Dumitrescu I, Onaca P, Serbanescu A, Nestorescu B.Accidental ethylmercury poisoning with nervous system, skeletal muscle, and myocardium injury.J Neurol Neurosurg Psychiatry 1980; 43:143-9.16) Bernard S, Enayati A, Redwood L, Roger H, Binstock T.Autism: A novel form of mercury poisoning..Med Hypotheses. 2001 Apr; 56(4):462-71.17) Holmes AS, Blaxill MF, Haley BE.Reduced levels of mercury in first baby haircuts of autistic children.Int J Toxic 2003; 22:277-85.18) Geier MR, Geier DA.Neurodevelopmental disorders following thimerosal-containing childhood vaccines..Exp Biol Med 2003; 228:660-419) Godfrey ME, Wojcik D, Krone

CA.Apolipoprotein E genotyping as a potential biomarker for mercury neurotoxicity.J Alzheimers Dis 2003; 5:189-196.20) Leong CWC, Syed NI, Lorscheider FL.Retrograde degeneration of neurite membrane structural integrity of nerve growth conesfollowing in vitro exposure to mercury.NeuroReport. 2001; 12:733-737.21) S. Makani, Sastry Gollapudi, Leman Yel, Shubpa Chiplunkar and Sudhir Gupta, “Biochemicaland molecular basis of thimerosal-induced apoptosis in T Cells: a major mole of mitochondrialpathway,†Genes and Immunity, 3(5), pages 270-278 (2002). [Thimerosal Effects at Parts perBillion]22) Mostafa Waly, Horatiu Olteanu, Ruma Banerjee, Sang-Woon Choi, Joel B. Mason, Belinda S.Parker, Saraswati Sukumar, S. Shim, Alok Sharma, Jorge M. Benzecry, V.-A. Power-Charnitskyand Richard C. Deth, IMMEDIATE COMMUNICATION, “Activation of methionine synthase byinsulin-like growth factor-1 and dopamine: a

target for neurodevelopmental toxins andthimerosal,†Molecular Psychiatry, pages 1-13 (January 27, 2004). [Confirmation of ThimerosalEffects at Parts per Billion]23) Christopher C. W Leong, Naweed I. Syed and Fritz L. Lorscheider, “Retrograde degeneration ofneurite membrane structural integrity of nerve growth cones following in vitro exposure tomercury,†NeuroReport, 12(4) pages 733-737 (2001). [ionic Mercury Effects at Parts per Trillion]24) Antonio R. Gasset, Motokazu Itoi, Yasuo Ishii and Richard M. Ramer, “Teratogenicities ofOphthalmic Drugs. II. Teratogenicities and Tissue Accumulation of Thimerosal,†Archives ofOphthalmology, 93, pages 52-55 (1975)25) Lyn Redwood, Sallie Bernard, and David Brown, “Predicted Mercury Concentrations in HairFrom Infant Immunizations: Cause for Concern,†NeuroToxicology, 22, pages 691-697 (2001).26) William Slikker, Jr., “Developmental Neurotoxicology Of

Therapeutics: Survey Of Novel RecentFindings,†NeuroToxicology, 21, page 250 (2000).27) Gregory V. Stajich, Gaylord P. Lopez, Sokei W.. Harry and William R. Sexson, “Iatrogenicexposure to mercury after hepatitis B vaccination in preterm infants,†The Journal ofPediatrics, 136(5), pages 679-681 (2000).28) Polly R. Sager (Corrected Slides), “Comparative Toxicokinetics of Methylmercury andThimerosal in Infant Macca fascicularis,†Institute of Medicine, National Academy of Sciences,Washington, DC, February 9, 2004.29) “Mercury: Medical and Public Health Issues,†a symposium that was held at the Tampa MarriottWaterside Hotel and Marina, Tampa, Florida, on April 28-30, 2004 and sponsored by the UnitedStates Department of Health and Human Services and the United States EnvironmentalProtection Agency.30) Subcommittee on Human Rights and Wellness, Committee on Government Reform of theHouse of

Representatives, “Mercury in Medicine Report,†Washington, DC, as published in theCongressional Record, pgs. E1011-E1030, May 21, 2003.31) U.S. Office of Special Counsel, 1730 M Street, N.W., Suite 218, Washington, D.C. 20036-4505,“OSC Forwards Public Health Concerns on Vaccines to Congress, …†For more informationplease visit our web site at http://www.osc.gov or call 1-800-872-9855.32) Special Counsel Scott Bloch’s letter to Congress addressed to: “The Honorable Judd Gregg,United States Senate, Chairman, Committee on Health, Education, Labor and Pensions, 428Dirksen Senate Office Building, Washington, D.C. 20510-6300 and The Honorable Joe Barton,U.S. House of Representatives, Chairman, Committee on Energy and Commerce, 2125 RayburnHouse Office Building, Washington, D.C. 20515†[OSC File Nos.: DI-04-1399, et al.]33) Thomas Verstraeten,

Robert Davis and Frank DeStefano, “Thimerosal VSD study, Phase I,Update, 02/29/00,†obtained by SafeMinds under FOIA in 2001. [Note: This draft ends with 5pages, having a footer notation of “LKLK03/28/00 … Response.doc,†and starting with a pageheading of “Thimerosal VSD study- Follow-up on conference call 03/02/2000,†that indicate theoverall document dates to the end of March 2000.]34) Thomas Verstraeten, Robert Davis, Frank DeStefano and the VSD team, “Risk of neurologicand renal impairment associated with thimerosal-containing vaccines,†obtained by SafeMindsunder FOIA in 2001.35) A copy of the printed Simpsonwood-meeting record (with an appended copy of the“Thimerosal VSD study, Phase I, Update, 02/29/00†document that is missing page 5, can befound on the Safe Minds website at http://www.safeminds.org/legislation/foia/simpsonwood.html..36) Mark Blaxill, Director, Safe Minds Analysis of Madsen et al., “Danish Thimerosal-Autism Studyin Pediatrics: Misleading and Uninformative on Autism-Mercury Link†(September 1, 2003), whoseobservations were determined by Dr Mark R. Geier and Mr. David A. Geier to apply to all of thestudies cited.37) Mark R. Geier and David A. Geier, “Neurodevelopmental Disorders after Thimerosal-ContainingVaccines: A BriefCommunication,†Society for Experimental Biology and Medicine, pages 660-664 (2003).38)MarkR.GeierandDavidA.Geier,“ThimerosalinChildhoodVaccines, Neurodevelopmental Disorders,and Heart Disease in the United States,†Journal of American Physicians and Surgeons, 8(1), pages6-11 (2003).39) David A. Geier and Mark R. Geier, “A comparative evaluation of the effects of MMRimmunization and mercury doses from

thimerosal-containing childhood vaccines on thepopulation prevalence of autism,†Medical Science Monitor, 10(3), pages P133-P139 (2004).40) E. A. Nelson and R. Y. Gottshall, “Enhanced Toxicity for Mice of Pertussis Vaccines WhenPreserved with Merthiolate,†Applied Microbiology, 15(3), pages 590-593 (1967).41) Martin F. Heyworth and Sidney C. Truelove, “Problems Associated With The Use OfMerthiolate As A Preservative In Anti-Lymphocytic Globulin,†Toxicology, 12, pages 325-333(1979).42) Lars Forstrom, M. Hannuksela, Merja Kousa and E. Lehmuskallio, “Merthiolatehypersensitivity and vaccination,†Contact Dermatitis, 6, pages 241-245 (1980).43) K. A. Winship, “Organic mercury compounds and their toxicity,†Adverse Drug Reaction AcutePoisoning Review, 3, pages 141-180 (1986).44) Neil H. Cox and Angela Forsyth, “Thiomersal allergy and vaccination reactions,†ContactDermatitis, 18, pages

229-233 (1988).45) Albert-Jan van’t Veen, “Vaccines Without Thiomersal Why So Necessary, Why So LongComing?,†Drugs, 61(5), pages 565-572 (2001).46) Leander Tryphonas and N. O. Nielsen, “Pathology of Chronic Alkylmercurial Poisoning inSwine, “American Journal of Veterinary Research, 34(3), pages 379-392 (1973).47) Laszlo Magos, A. W. Brown, S. Sparrow, E. Bailey, R. T. Snowden and W. R. Skipp, “Thecomparative toxicology of ethyl- and methylmercury.†Archives of Toxicology, 57, pages 260-267 (1985).48) The California OEHHA in a February 2004 document titled, “RESPONSE TO THE PETITIONOF BAYER CORPORATION FOR CLARIFICATION OF THE PROPOSITION 65 LISTING OF “MERCURYAND MERCURY COMPOUNDS†AS CHEMICALS KNOWN TO CAUSE REPRODUCTIVE TOXICITY.â€49) Mady Hornig, David Chian, and W. Ian Lipkin, IMMEDIATE COMMUNICATION, “Neurotoxiceffects of postnatal thimerosal are mouse strain dependent,â€

Molecular Psychiatry, pages 1-13,(Jun 8, 2004).50) Said Havarinasab, Lars Lambertsson, J. Qvarnstrom and Per Hultman, “Dose-response studyof thimerosal-induced murine systemic autoimmunity,†Toxicology and Applied Pharmacology, 194,pages 169-179 (2004).51) Woody R. McGinnis, “Mercury and Autistic Gut Disease,†Environmental Health Perspectives,109(7), pages A303-A304 (July 2001).52) “Biochemical Treatment Of Mental Illness And Behavior Disorders,†William J. Walsh, HealthResearch Institute, Presentation at Minnesota Brain Bio Association, November 1997.53) Director of Biological Sevices, Pittman-Moore Company, letter to Dr. Jamieson of Eli LillyCompany dated 1935. U.S. Congressional Record, May 21, 2003, E1018, page 9.54) Ueha-Ishibashi, et al. Effect of thimerosal, a preservative in vaccines, on intracellular Ca2+concentration of rat mcerebellar neurons. Toxicology.. 2004 Jan 15; 195(1):

77-8455) James SJ et al, Thimerosal neurotoxicity is associated with glutathione depletion: protectionwith glutathione precursors. Neurotoxicology. 2005 Jan;26(1):1-8.56) Kramer L, Bauer E, Jansen, M, Reiter D, Derfler K, Schaffer AMercury exposure in protein A immunoadsorptionNephro Dial Transplant 2004; 19:451-45657) Clarkson T, Magos L, Myers GThe Toxicology of Mercury-Current Exposures and Clinical ManifestationsNew England Journal of Medicine, October 200358)Burbacher T, Shen D, Liberato N, Grant K, Cernichiari E, Clarkson TComparison of Blood and Brain Mercury Levels in Infant Monkeys Exposed to Methylmercury orVaccines Containing ThimerosalEnvirn Health Perspect: doi:10.1289/ehp.7908 [online 20 April 2005]59) Torrente F, Anthony A, Heuschkel R, Thomsan M, Ashwood P, Murch SFocal-Enhanced Gastritis in Regressive Autism with Features Distinct from Crohn’s and HelibacterPylori

GastritisAmerican Journal of Gastroenterology 200460)Ashwood P, Murch S, Anthony A, Pellicer A, Torrente F, Thomsan M, Walker-Smith J, WakefieldAIntestinal Lymphocyte Populations in Children with Regressive Autism: Evidence for ExtensiveMucosal ImmunopathologyJournal of Clinical Immunology; Vol 23, No.6, November 200361)Torrente F, Ashwood P, Day R, Machado N, Furiano RI, Anthony A, Davis SE, Wakefield AJ,Thomson MA, Walker-Smith JA, Murch SHSmall Intestinal enteropathy with epithelial IgG and complement deposition in children withregressive autism62) Wakefield AJ, Anthony A, Murch SH, Thomson M, Montgomery SM, Davis S, et al.Enterocolitis in children with developmental disordersAm J Gastroenterol. 2000; 95:2285-228563) Horvath K, Papadimitriou J, Rabsztyn A, Drachenberg C, Tildon JTGastrointestinal abnormalities in children with autistic disorderJ Ped. 1999;135:559-56364) Furlano R,

Anthony A, Day R, Brown A, McGarvey L, Thomson M, Davies S, Berelowitz M,Forbes A, Wakefield A, Walker-Smith JA, Murch SColonic CD8 and Gamma Delta T-cell infiltration with epithelial damage in children with autism65) Ashwood, P, Anthony A, Torrente F, Wakefiel ASpontaneous Mucosal Lymphocyte Cytokine Profiles in Children with Autism and GastrointestinalSymptoms: Mucosal Immune Activation and Reduced Counter Regulatory Interleukin-10J clinical Immunology November 200466) Singh, VK, Lin SX, Yang VCSerological association of measles virus and human herpesvirus-6 with brain autoantibodies inautismClin Immunol Immunopathol. 1998;89:105-867) Singh VK, Jensen RLElevated levels of measles antibodies in children with autismPediatric Neurology, 2003; 28:292-29468) Uhlmann V, Martin CM, Sheils O, Pilkington L, Silva I, Killalea A, Murch SB, Walker-Smith J,Thomson M, Wakefield AJ, O’Leary

JJPotential viral pathogenic mechanism for a new variant inflammatory bowel diseaseMol Pathol. 2002 Apr;55(2):84-9069) Welch M, Welch-Horan T, Anwar M, Anwar N, Ludwig R, Ruggiero DBrain Effects of Chronic IBD in Areas Abnormal in Autism and Treatment by Single NeuropeptidesSecretin and OxytocinJournal of Molecular Neuroscience 2005. Vol 25 Number370) Sabra A, Bellanti J, Hartmann D, Zeligs B, MacDowell-Carneiro AL, Menendez F, Colon A, GuoWu A, Sabra LF, Romero M, Sabra S, Ebecken R, Madi KThe GUT-CNS Connection: a new Domain for the Clinician. Gastrointestinal and BehavioralDysfunction in Children with Non-IgE-mediated Food Allergy, Ileal-Nodular-Hyperplasia and LowTh1 Function: a New Clinical-Immunologic ConstellationAnnals of Allergy71) Humphrey Hl, Cole Mp, Pendergrass JC, Kiningham KKMitochondrial Mediated Thimerosal-Induced Apoptosis in Human Neuroblastoma Cell LineDept. of Pharmacology,

Joan C. Edwards School of Medicine, Marshall University, 1542 SpringValley Drive, Huntington, WV 2570472) Wakefield AJ, Murch SH, Anthony A, Linell J, Casson DM, Malik M, Berelowitz M, Dhillon AP,Thomson MA, Harvey P, Valentine A, Davies SE, Walker-Smith JAIleal lymphoid nodular hyperplasia, non-specific colitis and pervasive developmental disorder inchildrenLancet 1998; 351:637-64173) Singh, VK, Lin SX, Yang VCSerological association of measles virus and human herpesvirus-6 with brain autoantibodies inautismClin Immunol Immunopathol. 1998;89:105-874) Amaral DG, Corbett BA, Kantor AB, Becker C, Kakkanaiah V, Deng J, Bacalman S, Schulman HImmunophenotyping and Proteomic and Metabolic Profiling of Children with AutismM.I.N.D. Institute: abstract presented at IMFAR; May 200575) Vargas DL, Nascimbene C, Krishnan C, Zimmerman A, Pardo CNeuroglial Activation and Neuroinflammation in the Brain of

Patients with AutismAnnals of Neurology 2005:5776) Jyonouchi H, Geng L, Ruby A, Zimmerman-Bier BDysregulated Innate Immune Response in Young Children with Autism Spectrum Disorders: TheirRelationship to Gastrointestinal Symptoms and Dietary InterventionNeuropsychobiology 2005;51:77-85Hippocrates once said “Give me a fever and I can cure the childâ€. By understanding that a simple fever is a symptom rather than a condition orillness in itself, you soon come to realise that it is an ally and notan enemy. Fevers are the first sign that your child’s immune symptom isfunctioning as it should. By increasing core body temperature, feversenable the immune system to swing into action, indicating the body’sdefences are fighting an infection and consequent temperaturefluctuations indicate how the body is coping. - Natural

Parenting.

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