Norway Has 23 Case of H1N1, Decides to Vaccinate Entire Population

July 2, 2009

Infowars
June 2, 2009

Norway falls victim to the hype dished out by Big Pharma and its partner in crime, the U.N.’s World Health Organization. From the Norway Post:

The Norwegian health authorities will this fall begin a program of mass vaccination against the A H1N1 flu, also called the swine flu. A total of 9.4 million doses have been ordered from the suppliers.

All will be given two innoculations, two weeks apart, Bergens Tidende reports. The total cost will be NOK 650 million.

So far, only 23 cases of the flu has been diagnosed in Norway, but the authorities expect that the number will increase.

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Voluminous Research Proves Vaccines are Deadly

June 30, 2009
Infowars
June 30, 2009

An Infowars reader sent the following list of references proving vaccines are deadly. The next time somebody calls you a conspiracy nut for warning about vaccines, print out this list and give it to them.

Vaccines and Immunization References and Research Citations Vaccines Have Been Linked to Leukemias and Lymphomas:

Bichel, “Post-vaccinial Lymphadenitis Developing into Hodgkin’s Disease”, Acta Med Scand, 1976, Vol 199, p523-525.

Stewart, AM, et al, “Aetiology of Childhood Leukaemia”, Lancet, 16 Oct, 1965, 2:789-790. [Listed under Vaccine Adverse Reactions.]

Glathe, H et al, “Evidence of Tumorigenic Activity of Candidate Cell Substrate in Vaccine Production by the Use of Anti-Lymphocyte Serum”, Development Biol Std, 1977, 34:145-148.

Bolognesi, DP, “Potential Leukemia Virus Subunit Vaccines: Discussion”, Can Research, Feb 1976, 36(2 pt 2):655-656.

Colon, VF, et al, “Vaccinia Necrosum as a Clue to Lymphatic Lymphoma”, Geriatrics, Dec 1968, 23:81-82.

Park-Dincsoy, H et al, “Lymphoid Depletion in a case of Vaccinia Gangrenosa”, Laval Med, Jan 1968, 39:24-26.

Hugoson, G et al, “The Occurrence of Bovine Leukosis Following the Introduction of Babesiosis Vaccination”, Bibl Haemat, 1968, 30:157-161.

Hartstock, , “”Post-vaccinial Lymphadenitis: Hyperplasia of Lymphoid Tissue That Simulates Malignant Lymphomas”, Apr 1968, Cancer, 21(4):632-649.

Allerberger, F, “An Outbreak of Suppurative Lymphadenitis Connected with BCG Vaccination in Austria- 1990/1991,” Am Rev Respir Disorder, Aug 1991, 144(2) 469.

Omokoku B, Castells S, “Post-DPT inoculation cervical lymphadenitis in children.” N Y State J Med 1981 Oct;81(11):1667-1668. Vaccines and Chromosome Changes Leading to Mutations:

Knuutila, S et al, “An Increased Frequency of Chromosomal Changes and SCE’s in Cultured Lymphocytes of 12 Subjects Vaccinated Against Smallpox,” Hum Genet, 1978 Feb 23; 41(1):89-96.

Cherkeziia, SE, et al, “Disorders in the Murine Chromosome Apparatus Induced By Immunization with a Complex of Anti-viral Vaccines,” Vopr Virusol, 1979 Sept Oct, (5):547-550.

[Note: SCE means sister chromatid exchange and is an indication that genetic mutations are occurring, which could possibly lead to cancer-causing mutations. Vaccines and Auto-immunity Citations:

Romanov, V A, et al, “Role of Auto-immune Processes in the Pathogenesis of Post-Vaccinal Lesions of the Nervous System”, Oct 1977, Zh Mikrobiol Epidemiol Immunobiol, 10:80-83.

Grachev, V P, et al, “Formation of Auto-antibodies in Laboratory Animals After Inoculation of Viruses With Different Virulence. I. Results of Studies …, July 1973, Acta Virol (Praha), 17:319-326.

Movsesiants, AA, et al, “Experimental Study of the Ability of Different Strains of Vaccinia Virus to Induce Auto-Antibody Formation”, Vopr Virusol, May-Jun 1975; (3):297-302.

Negina, IuP, “Comparative Study of Auto-antibody Formation Following Immunization With Different Types of Typhoid Vaccines”, Zh Mikrobiol Epidemiol Immunobiol, May 1980; (5):69-72. Vaccinations and Diabetes Citations:

Sinaniotis, et al, “Diabetes Mellitus after Mumps Vaccination”, Arc Dis Child, 1975, 50:749.66

Polster, H, “Diabetes insipidus after Smallpox vaccination”, Z Aerztl Fortbild (Jena), 1 Apr 1966, 60:429-432.

Patan, “Postvaccinal Severe Diabetes Mellitus”, Ter Arkh, Jul 1968, 40:117-118.

Classen, JB, MD, “The Timing of Immunization Affects The Development of Diabetes in Rodents”, Autoimmunity, 1996, 24:137-145.

Classen JB, “The diabetes epidemic and the hepatitis B vaccines,” N Z Med J, 109(1030):366 1996 Sep 27. [letter]

Classen JB, “Childhood immunisation and diabetes mellitus,” N Z Med J, 109(1022):195 1996 May 24 [letter]

Poutasi K, ” Immunisation and diabetes,” N Z Med J 1996 Jul 26;109(1026):283. [letter; comment] Other Articles Linking Diabetes to Vaccines:

Dokheel, T M, “An Epidemic of Childhood Diabetes in the United States? Evidence from ….”, Diabetes Care, 1993, 16:1606-1611.

Parent ME, et al, “Bacille Calmette-Guerin vaccination and incidence of IDDM in Montreal, Canada,” Diabetes Care 1997 May; 20(5):767-772.

House DV, Winter WE, “Autoimmune diabetes. The role of auto-antibody markers in the prediction and prevention of insulin-dependent diabetes mellitus,” Clin Lab Med 1997 Sep; 17(3):499-545.

Zeigler, M et al , “[Autoantibodies in type 1 diabetes mellitus]” Z Arztl Fortbild (Jena). 1994 Aug; 88(7-8):561-5 Vaccines and Nervous System Changes:

Bondarev, VN et al, “The Changes of the Nervous System in Children After Vaccination”, Pediatria, Jun 1969; 48:20-24.

Ehrengut W, “Central nervous sequelae of vaccinations,” Lancet 1986 May 31;1(8492):1275-1276.

Provvidenza, G et al, [On a Case of Benign Acute Cerebellar Ataxia in Childhood], Arch Ital Sci Med Trop, 43:189-194, Apr 1962.

Katsilambros, L, “[The Phenomenom of Apathy in Man and Animals After the Injection of Viruses in Very High Doses. Clinical Data]“, Rev Med Moyen Orient, 20:539-546, Nov – Dec 1963. Vaccinations and Autism Citations:

Eggers, C, “Autistic Syndrome (Kanner) And Vaccinations against Smallpox”, Klin Paediatr, Mar 1976, 188(2):172-180.

Kiln MR, “Autism, inflammatory bowel disease, and MMR vaccine.” Lancet 1998 May 2;351(9112):1358.

Selway, “MMR vaccination and autism 1998. Medical practitioners need to give more than reassurance.” BMJ 1998 Jun 13;316(7147):1824.

Nicoll A, Elliman D, Ross E, “MMR vaccination and autism 1998,” MJ 1998 Mar 7;316(7133):715-716.

Lindley K J, Milla PJ, “Autism, inflammatory bowel disease, and MMR vaccine.”Lancet 1998 Mar 21;351(9106):907-908.

Bedford H, et al, “Autism, inflammatory bowel disease, and MMR vaccine.” Lancet 1998 Mar 21;351(9106):907.

Vijendra K. Singh, Sheren X. Lin, and Victor C. Yang, “Serological Association of Measles Virus and Human Herpesvirus-6 with Brain Autoantibodies in Autism,” Clinical Immunology and Immunopathology, Oct 1998, Vol. 89, No. 1, p 105-108. [“None of the autistic children in the study had measles in the past, but all had the MMR” stated David Whalgren. Vaccines and Demyelination Citations:

Herroelen, L et al, “Central-Nervous-System Demyelination After Immunization with Recombinant Hepatitis B Vaccine”, Lancet, Nov 9, 1991, 338(8776):1174-1175.

Kaplanski G, Retornaz F, Durand J, Soubeyrand J, “Central nervous system demyelination after vaccination against hepatitis B and HLA haplotype.” J Neurol Neurosurg Psychiatry 1995 Jun; 58(6):758-759.

Matyszak MK, Perry VH, “Demyelination in the central nervous system following a delayed-type hypersensitivity response to bacillus Calmette-Guerin.” Neuroscience 1995 Feb;64(4):967-977.

Tornatore CS, Richert JR, “CNS demyelination associated with diploid cell rabies vaccine.” Lancet 1990 Jun 2;335(8701):1346-1347.

Adams, JM et al, “Neuromyelitis Optica: Severe Demyelination Occurring Years After Primary Smallpox Vaccinations”, Rev Roum Neurol, 1973, 10:227-231.

In 1988, Dietrich used MRI to show that developmentally delayed children had alterations in their myelin. Coulter described that central nervous system damage can be exhibited as abnormal behavior of the child. In 1935, Thomas Rivers, experimental allergic encephalitis (EAE) can be the result of a viral or bacterial infection of the nervous system. “The fact of the matter is that it is a matter of record that it was known that vaccination produced encephalitis since 1926.” The authors stated, “In regions in which there is no organized vaccination of the population, general paralysis is rare. … It is impossible to deny a connection between vaccinations and the encephalitis (brain damage) which follows it.” Vaccines have been linked to seizures, convulsions and epilepsy. Vaccinations and Seizures:

Hirtz DG, Nelson KB, Ellenberg J H, “Seizures following childhood immunizations”, Pediatr 1983 Jan; 102(1):14-18.

Cherry JD, Holtzman AE, Shields WD, Buch D, Nielsen, “Pertussis immunization and characteristics related to first seizures in infants and children,”J Pediatr 1993 Jun;122(6):900-903.

Coplan J, “Seizures following immunizations,” J Pediatr 1983 Sep;103(3):496.

Barkin RM, Jabhour JT, Samuelson J S, “Immunizations, seizures, and subsequent evaluation,” JAMA 1987 Jul 10;258(2):201.

Griffin MR, et al, “Risk of seizures after measles-mumps-rubella immunization,” Pediatrics 1991 Nov;88(5):881-885.

Griffin MR, et al, “Risk of seizures and encephalopathy after immunization with the diphtheria-tetanus-pertussis vaccine,” JAMA 1990 Mar 23-30;263(12):1641-1645.

Cizewska S, Huber Z, Sluzewski W, “[Prophylactic inoculations and seizure activity in the EEG],” Neurol Neurochir Pol 1981 Sep-Dec;15(5-6):553-557. [Article in Polish]

Huttenlocher PR, Hapke RJ, “A follow-up study of intractable seizures in childhood.” Ann Neurol 1990 Nov; 28(5):699-705.

Blumberg DA, “Severe reactions associated with diphtheria-tetanus-pertussis vaccine: detailed study of children with seizures, hypotonic-hypo-responsive episodes, high fevers, and persistent crying.”Pediatrics 1993 Jun; 91(6):1158-1165. Vaccinations and Convulsions Citations:

Prensky AL, et al, “History of convulsions and use of pertussis vaccine,” J Pediatr 1985 Aug; 107(2):244-255.

Baraff LJ, “Infants and children with convulsions and hypotonic-hypo-responsive episodes following diphtheria-tetanus-pertussis immunization: follow-up evaluation,” Pediatrics 1988 Jun; 81(6):789-794.

Jacobson V, “Relationship of pertussis immunization to the onset of epilepsy, febrile convulsions and central nervous system infections: a retrospective epidemiologic study,” Tokai J Exp Clin Med 1988;13 Suppl: 137-142.

Cupic V,et al, “[Role of DTP vaccine in the convulsive syndromes in children],” Lijec Vjesn 1978 Jun; 100(6):345-348. [Article in Serbo-Croatian (Roman)]

Pokrovskaia NIa, “[Convulsive syndrome in DPT vaccination (a clinico-experimental study)],” Pediatriia 1983 May;(5):37-39. [Article in Russian] Vaccinations and Epilepsy Citations:

Ballerini, Ricci, B, et al, “On Neurological Complications of Vaccination, With Special Reference to Epileptic Syndromes,” Riv Neurol, Jul-Aug 1973, 43:254-258.

Wolf SM, Forsythe A, “Epilepsy and mental retardation following febrile seizures in childhood,” Acta Paediatr Scand 1989 Mar;78(2):291-295. ________________________________________ Vaccines and Brain Swelling:

Iwasa, S et al, “Swelling of the Brain in Mice Caused by Pertussis … Quantitative Determination and the Responsibility of the Vaccine”, Jpn J Med Sci Biol, 1985 , 38(2):53-65.

Mathur R, Kumari S, “Bulging fontanel following triple vaccine.” Indian Pediatr 1981 Jun;18(6):417-418.

Barry W, Lenney W, Hatcher G, “Bulging fontanelles in infants without meningitis.” Arch Dis Child 1989 Apr;64(4):635-636.

Shendurnikar N, “Bulging fontanel following DPT” Indian Pediatr 1986 Nov;23(11):960.

Gross TP, Milstien JB, Kuritsky JN, “Bulging fontanelle after immunization with diphtheria-tetanus-pertussis vaccine and diphtheria-tetanus vaccine.” J Pediatr 1989 Mar;114(3):423-425.

Jacob J, Mannino F, “Increased intracranial pressure after diphtheria, tetanus, and pertussis immunization.” Am J Dis Child 1979 Feb;133(2):217-218.

Dugmore, WN, “Bilateral Oedema at the Posterior Pole. Hypersensitivity Reaction to Alavac P injection.” Br J Ophthalmol, Dec 1972, 55:848-849. Vaccines and Neurological Damage

Nedar P R, and Warren, R J, “Reported Neurological Disorders Following Live Measles Vaccine”, 1968, Ped, 41:997-1001.

Paradiso, G et al, “Multifocal Demyelinating Neuropathy after Tetanus Vaccine”, Medicina (B Aires), 1990, 50(1):52-54.

Landrigan, PJ, Whitte, J, “Neurologic Disorders Following Live Measles-virus Vaccination”, JAMA, Mar 26, 1973, v223(13):1459-1462.

Turnbull, H M, “Encephalomyelitis Following Vaccination”, Brit Jour Exper Path, 7:181, 1926.

Kulenkampff, M et al, “Neurological Complications of Pertussis Inoculation”, Arch Dis Child, 1974, 49:46.

Strom, J, “Further Experience of Reactions, Especially of a Cerebral Nature in Conjunction with Triple Vaccination”, Brit Med Jour, 1967, 4:320-323.

Berg, J M, “Neurological Complications of Pertussis Immunization,” Brit Med Jour, July 5,1958; p 24.

Bondarev, VN et al, “The Changes of the Nervous System in Children After Vaccination”, Pediatria, Jun 1969; 48:20-24.

Badalian, LO, “Vaccinal Lesions of the Nervous System in Children,” Vop Okhr Materin Dets, Dec 1959, 13:54-59

Lorentz, IT, et al, “Post-Vaccinal Sensory Polyneuropathy with Myoclonus”, Proc Aust Ass Neurol, 1969, 6:81-86.

Trump, R C, White, T R, “Cerebellar Ataxia Presumed Due To Live Attenuated Measles Virus Vaccine,” JAMA, 1967, 199:165-166.

Allerdist, H, “Neurological Complications Following Measles Vaccination”, Inter Symp, Brussels, 1978, Development Biol Std, Vol 43, 259-264.

Finley, K H, “Pathogenesis of Encephalitis Occurring With Vaccination, Variola and Measles, Arch Neur and Psychologist, 1938; 39:1047-1054.

Froissart, M et al, “Acute Meningoencephalitis Immediately after an Influenza Vaccination”, Lille Med, Oct 1978, 23(8):548-551.

Pokrovskaia, Nia, et al, “Neurological Complications in Children From Smallpox Vaccination”, Pediatriia, Dec 1978, (12):45-49.

Allerdist, H, “Neurological Complications Following Measles Virus Vaccination. Evaluation of the Cases seen Between 1971-1977″, Monatsschr Kinderheilkd, Jan 1979, 127(1): 23-28.

Ehrengut, W et al, “On Convulsive Reactions Following Oral vaccination Against Polio”, Klin Paediatr, May 1979, 191(3):261-270.

Naumova, R P, et al, “Encephalitis Developing After Vaccination without a Local Skin Reaction”, Vrach Delo, Jul 1979, (7):114-115.

Goswamy, BM, “Neurological Complications After Smallpox Vaccination”, J Ass Phys India, Jan 1969, 17:41-43.

Schchelkunov, SN et al, “The Role of Viruses in the Induction of Allergic Encephalomyelitis,” Dokl Akad Nauk SSSR, 1990,315(1):252-255. [Vaccines contain viruses, too]

Walker AM, “Neurologic events following diphtheria-tetanus-pertussis immunization,” Pediatrics 1988 Mar;81(3):345-349.

Shields WD, et al, “Relationship of pertussis immunization to the onset of neurologic disorders: a retrospective epidemiologic study,” J Pediatr 1988 Nov; 113(5):801-805.

Wilson J, “Proceedings: Neurological complications of DPT inoculation in infancy,” Arch Dis Child 1973 Oct; 48(10):829-830.

Iakunin IuA, “[Nervous system complications in children after preventive vaccinations],” Pediatriia 1968 Nov; 47(11):19-26. [Article in Russian]

Greco D, et al, “Case-control study on encephalopathy associated with diphtheria-tetanus immunization in Campania, Italy,” Bull World Health Organ 1985;63(5):919-925.

Ehrengut W at Institute of Vaccinology and Virology, Hamburg, Germany states, “Bias in the evaluation of CNS complications following pertussis immunization are the following: 1) Notifications of post-immunization adverse events, 2) Publications by vaccine producers on the frequency of adverse reactions, 3) Comparison of permanent brain damage after DPT and DT immunization, 4) Pro-immunization, 5) Immunization associated viral encephalitis, 6) Accuracy of statistics, 7) Personal. A review of these points indicates an underestimation of CNS complications after pertussis immunization.”

Reference: Ehrengut W, “Bias in evaluating CNS complications following pertussis immunization.” Acta Paediatr Jpn, 1991 Aug; 33(4):421-427. Vaccinations and Unexplained Diseases:

Hiner, E E, Frasch, C E, “Spectrum of Disease Due to Haemophilus Influenza Type B Occurring in Vaccinated Children”, J Infect Disorder, 1988 Aug; 158(2): 343-348.

Olin P, Romanus, V, Storsaeter, J, “Invasive Bacterial Infections During an Efficiacy Trial of Acellular Pertussis Vaccines — Implications For Future Surveilance In Pertussis Vaccine Programmes”, Tokai J Exp Clin Med, 1988; 13 Suppl: 143-144.

Storsaeter, J, et al, “Mortality and Morbidity From Invasive Bacterial Infections During a Clinical Trial of Acellular Pertussis Vaccines in Sweden”, Pediatr Infect Disorder J, 1988 Sept; 7(9):637-645.

Vadheim, CM, et al, “Effectiveness and Safety of an Haemophilus Influenzae type b Conjugate Vaccine (PRP-T) in Young Infants. Kaiser-UCLA Vaccine Study Group,” Pediartics, 1993 Aug; 92(2):272-279. [The vaccines caused fevers, irritability, crying, and seizures, but were declared to be “safe and … effective … “.]

Stickl, H, “Estimation of Vaccination Damage”, Med Welt, Oct 14, 1972, 23:1495-1497.

Waters, VV, et al, “Risk Factors for Measles in a Vaccinated Population”, JAMA, Mar 27, 1991, 265(12): 1527.

Stickl, H, “Iatrogenic Immuno-suppression as a Result of Vaccination”, Fortschr Med, Mar 5, 1981, 99(9);289-292. Vaccine Citations Linking the Vaccine to the “prevented” Disease:

Nkowane, et al, “Vaccine-Associated Paralytic Poliomyelitis, US 1973 through 1984, JAMA, 1987, Vol 257:1335-1340.

Quast, et al, “Vaccine Induced Mumps-like Diseases”, nd, Int Symp on Immun, Development Bio Stand, Vol 43, p269-272.

Green, C et al, “A Case of Hepatitis Related to Etretinate Therapy and Hepatitis B Vaccine”, Dermatologica, 1991, 182(2):119-120.

Shasby, DM, et al, “Epidemic Measles in Highly Vaccinated Population”, NEJM, Mar 1977, 296(11): 585-589.

Tesovic, G et al, “Aseptic Meningitis after Measles, Mumps and Rubella Vaccine”, Lancet, Jun 12, 1993, 341(8859):1541.

Johnson, RH, et al, “Nosocomial Vaccinia Infection”, West J Med, Oct 1976, 125(4):266-270.

Malengreau, M, “Reappearance of Post-Vaccination Infection of Measles, Rubella, and Mumps. Should Adolescents be re-vaccinated?” Pedaitric, 1992;47(9):597-601 (25 ref)

Basa, SN, “Paralytic Poliomyelitis Following Inoculation With Combined DTP Prophylactic. A review of Sixteen cases with Special Reference to Immunization Schedules in Infancy”, J Indian Med Assoc, Feb 1, 1973, 60:97-99.

Landrigan, PJ et al, “Measles in Previously Vaccinated Children in Illinois”, Ill Med J, Arp 1974, 141:367-372.

NA, “Vaccine-Associated Poliomyelitis”, Med J Aust, Oct 1973, 2:795-796. Vaccine Failures Citations:

Hardy, GE, Jr, et al, “The Failure of a School Immunization Campaign to Terminate an Urban Epidemic of Measles,” Amer J Epidem, Mar 1970; 91:286-293.

Cherry, JD, et al, “A Clinical and Serologic Study of 103 Children With Measles Vaccine Failure”, J Pediatr, May 1973; 82:801-808.

Jilg, W, et al, “Inoculation Failure Following Hepatitis B Vaccination”, Dtsch Med wochenschr, 1990 Oct 12; 115(41):1514-1548.

Plotkin, SA, “Failures of Protection by Measles Vaccine,” J Pediatr, May 1973; 82:798-801.

Bolotovskii, V, et al, “Measles Incidence Among Children Properly Vaccinated Against This Infection”, ZH Mikrobiol Epidemiol Immunobiol, 1974; 00(5):32-35.

Landrigan, PJ, et al, “Measles in Previously Vaccinated Children in Illinois”, Ill Med J, Apr 1974; 141:367-372.

Strebel, P et al, “An Outbreak of Whooping Cough in a Highly Vaccinated Urban Community”, J Trop Pediatr, Mar 1991, 37(2): 71-76.

Forrest, JM, et al, “Failure of Rubella Vaccination to Prevent Congenital Rubella,”Med J Aust, 1977 Jan 15; 1(3): 77.

Jilg, W, “Unsuccessful Vaccination against Hepatitis B”, Dtsch Med Wochenschr, Nov 16, 1990, 115(46):1773.

Coles, FB, et al, “An Outbreak of Influenza A (H3N2) in a Well-Immunized Nursing home Population,” J Am ger Sociologist, Jun 1992, 40(6):589-592.

Jilg, W, et al, “Inoculation Failure following Hepatitis B Vaccination,” Dtsch Med Wochenschr, Oct 12, 1990, 115(41):1545-1548.

Hartmann, G et al, “Unsuccessful Inoculation against Hepatitis B,” Dtsch Med Wochenschr, May 17, 1991, 116(20): 797.

Buddle, BM et al, “Contagious Ecthyma Virus-Vaccination Failures”, Am J Vet Research, Feb 1984, 45(2):263-266.

Mathias, R G, “Whooping Cough In Spite of Immunization”, Can J Pub Health, 1978 Mar/Apr; 69(2):130-132.

Osterholm, MT, et al, “Lack of Efficacy of Haemophilus b Polysacharide Vaccine in Minnesota”, JAMA, 1988 Sept 9; 260(10:1423-1428.

Johnson, RH, et al, “Nosocomial Vaccinia Infection”, West J Med, Oct 1976, 125(4):266-270. Vaccines Causing Another Vaccinal Disease:

Basa, SN, “Paralytic Poliomyelitis Following Inoculation With Combined DTP Prophylactic. A review of Sixteen cases with Special Reference to Immunization Schedules in Infancy”, J Indian Med Assoc, Feb 1, 1973, 60:97-99.

Pathel, JC, et al, “Tetanus Following Vaccination Against Small-pox”, J Pediatr, Jul 1960; 27:251-263.

Favez, G, “Tuberculous Superinfection Following a Smallpox Re-Vaccination”, Praxis, July 21, 1960; 49:698-699.

Quast, Ute, and Hennessen, “Vaccine-Induced Mumps-like Diseases”, Intern Symp on Immunizations , Development Bio Stand, Vol 43, p 269-272.

Forrest, J M, et al, “Clinical Rubella Eleven months after Vaccination,” Lancet, Aug 26, 1972, 2:399-400.

Dittman, S, “Atypical Measles after Vaccination”, Beitr Hyg Epidemiol, 19891, 25:1-274 (939 ref)

Sen S, et al, “Poliomyelitis in Vaccinated Children”, Indian Pediatr, May 1989, 26(5): 423-429.

Arya, SC, “Putative Failure of Recombinant DNA Hepatitis B Vaccines”, Vaccine, Apr 1989, 7(2): 164-165.

Lawrence, R et al, “The Risk of Zoster after Varicella Vaccination in Children with Leukemia”, NEJM, Mar 3, 1988, 318(9): 543-548. Vaccination Citations and Death

Na, “DPT Vaccination and Sudden Infant Death – Tennessee, US Dept HEW, MMWR Report, Mar 23, 1979, vol 28(11): 132.

Arevalo, “Vaccinia Necrosum. Report on a Fatal Case”, Bol Ofoc Sanit Panamer, Aug 1967, 63:106-110.

Connolly, J H, Dick, G W, Field, CM, “A Case of Fatal Progressive Vaccinia”, Brit Med Jour, 12 May 1962; 5288:1315-1317.

Aragona, F, “Fatal Acute Adrenal Insufficiency Caused by Bilateral Apoplexy of the Adrenal Glands (WFS) following Anti-poliomyelitis Vaccination”, Minerva Medicolegale, Aug 1960; 80:167-173.

Moblus, G et al, “Pathological-Anatomical Findings in Cases of Death Following Poliomyelitis and DPT Vaccination”, Dtsch Gesundheitsw, Jul 20, 1972, 27:1382-1386.

NA, “Immunizations and Cot Deaths”, Lancet, Sept 25, 1982, np.

Goetzeler, A, “Fatal Encephalitis after Poliomyelitis Vaccination”, 22 Jun 1961, Muenchen Med Wschr, 102:1419-1422.

Fulginiti, V, “Sudden Infant Death Syndrome, Diphtheria-Tetanus Toxoid-Pertussis Vaccination and Visits to the Doctor: Chance Association or Cause and Effect?”, Pediatr Infect Disorder, Jan-Feb 1983, 2(1): 7-11.

Baraff, LJ, et al, “Possible Temporal Association Between Diphtheria-tetanus toxoid-Pertussis Vaccination and Sudden Infant Death Syndrome”, Pediatr Infect Disorder, Jan-Feb 1983, 2(1): 5-6.

Reynolds, E, “Fatal Outcome of a Case of Eczema Vaccinatum”, Lancet, 24 Sept 1960, 2:684-686.

Apostolov. et al, “Death of an Infant in Hyperthermia After Vaccination”, J Clin Path, Mar 1961, 14:196-197.

Bouvier-Colle, MH, “Sex-Specific Differences in Mortality After High-Titre Measles Vaccination”, Rev Epidemiol Sante Publique, 1995; 43(1): 97.

Stewart GT, “Deaths of infants after triple vaccine.”, Lancet 1979 Aug 18;2(8138):354-355.

Flahault A, “Sudden infant death syndrome and diphtheria/tetanus toxoid/pertussis/poliomyelitis immunisation.”, Lancet 1988 Mar 12;1(8585):582-583.

Larbre, F et al, “Fatal Acute Myocarditis After Smallpox Vaccination”, Pediatrie, Apr-May 1966, 21:345-350.

Mortimer EA Jr, “DTP and SIDS: when data differ”, Am J Public Health 1987 Aug; 77(8):925-926. Vaccines and Metabolism Citations:

Deutsch J, ” [Temperature changes after triple-immunization in infant age],” Padiatr Grenzgeb 1976;15(1):3-6. [Article in German]

NA, “[Temperature changes after triple immunization in childhood],” Padiatr Grenzgeb 1976;15(1):7-10. [Article in German]

[Considering that the thyroid controls our Basal Metabolism, it would appear that vaccines altered (depressed) thyroid activity.] Vaccines Altering Resistance to Disease:

Burmistrova AL, “[Change in the non-specific resistance of the body to influenza and acute respiratory diseases following immunization diphtheria-tetanus vaccine],” Zh Mikrobiol Epidemiol Immunobiol 1976; (3):89-91. [Article in Russian] Vaccinations and Deafness Citations: So I did a background check to see if there was any scientific evidence linking vaccines to deafness and hearing loss. Here are some of the articles I found:

Kaga, “Unilateral Total Loss of Auditory and Vestibular Function as a Complication of Mumps Vaccination”, Int J Ped Oto, Feb 1998, 43(1):73-73

Nabe-Nielsen, Walter, “Unilateral Total Deafness as a Complication of the Measles- Mumps- Rubella Vaccination”, Scan Audio Suppl, 1988, 30:69-70

Hulbert, et al, “Bilateral Hearing Loss after Measles and Rubella Vaccination in an Adult”, NEJM, 1991 July, 11;325(2):134

Healy, “Mumps Vaccine and Nerve Deafness”, Am J Disorder Child, 1972 Jun; 123(6):612

Jayarajan, Sedler, “Hearing Loss Following Measles Vaccination”, J Infect, 1995 Mar; 30(2):184-185

Pialoux, P et al, “Vaccinations and Deafness”, Ann Otolaryng (Paris), Dec 1963, 80:1012-1013.

Angerstein, W, et al, “Solitary Hearing and Equilibrium Damage After Vaccinations”, Gesundheitswesen, May 1995, 57(5): 264-268.

Brodsky, Stanievich, “Sensorineural Hearing Loss Following Live Measles Virus Vaccination”, Int J Ped Oto, 1985 Nov; 10(2):159-163

Koga, et al, “Bilateral Acute Profound Deafness After MMR Vaccination- Report of a Case”, Nippon Jibiin Gakkai Kai, 1991 Aug;94(8):1142-5

Seiferth, LB, “Deafness after Oral Poliomyelitis Vaccination – a Case Report and Review”, HNO, 1977 Aug; 25(8): 297-300

Pantazopoulos, PE, “Perceptive Deafness Following Prophylactic use of Tetanus anittoxin”, Laryngoscope, Dec 1965, 75:1832-1836.

Zimmerman, W, “Observation of a case of Acute Bilateral Hearing Impairment Following Preventive Poliomyelitis Vaccination (type 3)”, Arch Ohr Nas Kehlkopfheilk, 1965, 185:723-725. Vaccinations and Kidney Disorders Citations:

Jacquot, C et al, “Renal Risk in Vaccination”, Nouv Presse Med, Nov 6, 1982, 11(44):3237-3238.

Giudicelli, et al, “Renal Risk in Vaccination”, Presse Med, Jun 11, 1982, 12(25):1587-1590.

Tan, SY, et al, “Vaccine Related Glomerulonephritis”, BMJ, Jan 23, 1993, 306(6872):248.

Pillai, JJ, et al, “Renal Involvement in Association with Post-vaccination Varicella”, Clin Infect Disorder, Dec 1993, 17(6): 1079-1080.

Eisinger, AJ et al, “Acute Renal Failure after TAB and Cholera Vaccination”, B Med J, Feb 10, 1979, 1(6160):381-382.

Silina, ZM, et al, “Causes of Postvaccinal Complications in the Kidneys in Young Infants”, Pediatria, Dec 1978, (12):59-61.

Na, “Albuminurias”, Concours Med, Mar 1964, 85:5095-5098. [vaccination adverse reactions]

Oyrl, A, et al, “Can Vaccinations Harm the Kidney?”, Clin Nephrol, 1975, 3(5):204-205.

Mel’man Nia, “[Renal lesions after use of vaccines and sera].” Vrach Delo 1978 Oct;(10):67-9, [Article in Russian]

Silina ZM, Galaktionova TIa, Shabunina NR, “[Causes of postvaccinal complications in the kidneys in young infants].” Pediatriia 1978 Dec;(12):59-61, [Article in Russian]

Silina EM, et al, “[Some diseases of the kidneys in children during the 1st year of life, following primary smallpox vaccination and administration of pertusis-diphtheria-tetanus vaccine].” Vopr Okhr Materin Det 1968 Mar; 13(3):79-80, [Article in Russian] Vaccines and Skin Disorders Citations:

Illingsworth R, Skin rashes after triple vaccine,” Arch Dis Child 1987 Sep; 62(9):979.

Lupton GP, “Discoid lupus erythematosus occurring in a smallpox vaccination scar,” J Am Acad Dermatol, 1987 Oct; 17(4):688-690.

Kompier, A J, “Some Skin Diseases caused by Vaccinia Virus [Smallpox],” Ned Milt Geneesk T, 15:149-157, May 1962.

Weber, G et al, “Skin Lesions Following Vaccinations,” Deutsch Med Wschr, 88:1878-1886, S7 Sept 1963.

Copeman, P W, “Skin Complications of Smallpox Vaccination,” Practitioner, 197:793-800, Dec 1966.

Denning, DW, et al, “Skin Rashes After Triple Vaccine,” Arch Disorder Child, May 1987, 62(5): 510-511. Vaccinations and Abcesses:

Sterler, HC, et al, “Outbreaks of Group A Steptococcal Abcesses Following DTP Vaccination”, Pediatrics, Feb 1985, 75(2):299-303.

DiPiramo, D, et al, “Abcess Formation at the Site of Inoculation of Calmette-Guerin Bacillus (BCG),” Riv Med Aeronaut Spaz, Jul-Dec 1981, 46(3-4):190-199. Vaccinations and Shock:

Caileba, A et al, “Shock associated with Disseminated Intravascular Coagulation Syndrome following Injection of DT.TAB Vaccine, Prese Med, Sept 15, 1984, 13(3):1900. Vaccines: The Weird, The Wild and The Hilarious Citations: Sometimes there are articles published about the strangest facts related to vaccines that defies our imagination and ability to understand them. They were written seriously by well-meaning scientific persons, but their titles can be seen differently. Some are funny, some are sad and some are purely scientific folly. See if you can figure these out:

Pathel, JC, et al, “Tetanus Following Vaccination Against Small-pox”, J Pediatr, Jul 1960; 27:251-263. [Now you need a tetanus vaccination!]

Favez, G, “Tuberculous Superinfection Following a Smallpox Re-Vaccination”, Praxis, July 21, 1960; 49:698-699. [Super means large/big/great!]

Bonifacio, A et al, “Traffic Accidents as an expression of “Iatrogenic damage”, Minerva Med, Feb 24, 1971, 62:735-740. [But officer I was just vaccinated!]

Baker, J et al, “Accidental Vaccinia: Primary Inoculation of a Scrotum”, Clin Pediatr (Phila), Apr 1972, 11:244-245. [Ooops, the needle slipped.]

Edwards, K, “Danger of Sunburn Following Vaccination”, Papua New Guinea Med J, Dec 1977, 20(4):203. [Are vaccines phototoxic?]

Stroder, J, “Incorrect Therapy in Children”, Folia Clin Int (Barc), Feb 1966, 16:82-90. [Agreed.]

Wehrle PF, “Injury associated with the use of vaccines,” Clin Ther 1985;7(3):282-284. [Dah!]

Alberts ME, “When and where will it stop”, Iowa Med 1986 Sep; 76(9):424. [When!]

Breiman RF, Zanca JA, “Of floors and ceilings — defining, assuring, and communicating vaccine safety”, Am J Public Health 1997 Dec;87(12):1919-1920. [What is in between floors and ceilings?]

Stewart, AM, et al, “Aetiology of Childhood Leukaemia”, Lancet, 16 Oct, 1965, 2:789-790.

Nelson, ST, “John Hutchinson On Vaccination Syphilis (Hutchinson, J)”, Arch Derm, (Chic), May 1969, 99:529-535. [Vaccinations and STDs!]

Mather, C, “Cotton Mather Anguishes Over the Consequences of His Son’s Inoculation Against Smallpox”, Pediatrics, May 1974; 53:756. [Is it for or against?]

Thoman M, “The Toxic Shot Syndrome”, Vet Hum Toxicol, Apr 1986, 28(2):163-166. [Animals are not exempt from vaccination damage either!]

Johnson, RH, et al, “Nosocomial Vaccinia Infection”, West J Med, Oct 1976, 125(4):266-270. [Nosocomial means a disease acquired in a doctor’s office or hospital.]

Heed, JR, “Human Immunization With Rabies Vaccine in Suckling Mice Brain,” Salud Publica, May-Jun 1974, 16(3): 469-480. [Have you had your suckling mice brains today?]

Tesovic, G et al, “Aseptic Meningitis after Measles, Mumps and Rubella Vaccine”, Lancet, Jun 12, 1993, 341(8859):1541. [AM has same symptoms as poliomyelitis!]

Buddle, BM et al, “Contagious Ecthyma Virus-Vaccination Failures”, Am J Vet Research, Feb 1984, 45(2):263-266.

Freter, R et al, “Oral Immunization And Production of Coproantibody in Human Volunteers”, J Immunol, Dec 1963, 91:724-729. [Guess what copro- means …. Feces.]

NA, “Vaccination, For and Against”, 1964, Belg T Geneesk, 20:125-130. [Is it for or against?]

Sahadevan, MG et al, “Post-vaccinal Myelitis”, J Indian Med Ass, Feb 16, 1966, 46:205-206. [Did I mention myelitis?]

Castan, P et al, “Coma Revealing an acute Leukosis in a child, 15 days after an Oral Anti-poliomyelitis Vaccination,” Acta Neurol Bekg, May 1965, 65:349-367. [Coma from vaccines!]

Stickl, H, et al, “Purulent [pus] meningitides Following Smallpox Vaccination. On the Problem of Post- Vaccinal Decrease of Resistance”, Deutsch Med Wschr, Jul 22, 1966, 91:1307-1310. [Vaccines are the injection of viruses cultured from pus … ]

Haas, R


Innoculations: The True Weapons Of Mass Destruction

June 28, 2009
Rebecca Carley, M.D.
Infowars
June 28, 2009

“One basic truth can be used as a foundation for a mountain of lies, and if we dig down deep enough in the mountain of lies, and bring out that truth, to set it on top of the mountain of lies; the entire mountain of lies will crumble under the weight of that one truth. And there is nothing more devastating to a structure of lies than the revelation of the truth upon which the structure of lies was built, because the shock waves of the revelation of the truth reverberate, and continue to reverberate throughout the Earth for generations to follow, awakening even those people who had no desire to be awakened to the truth.” (by Delamar Duvaris as written in the preface of “Behold the Pale Horse” by William Cooper).

The basic truth that served as the foundation for the mountain of lies known as vaccinations was the observation that mammals who recover from infection with microorganisms acquire natural immunity from further infections. Whenever T cells (the little packman cells which kill viruses, bacteria, and cancer cells, thus conferring cellular immunity) and B cells (antibody producing cells which confer humoral immunity) are activated by various substances foreign to the body called antigens, some of the T and B cells become memory cells. Thus, the next time the individual meets up with that same antigen, the immune system can be quickly triggered to demolish it. This is the process known as immunity.

This truth gave birth to a beLIEf that if a foreign antigen was injected into an individual, that individual would then become immune to a future infection. This beLIEf, (you see the lie in the middle), was given the name, “vaccinations”. What the promoters of vaccination failed to realize is that the respiratory tract of ALL mammals (since animals are just as devastated by these inoculations with disease as are humans) contain secretory IgA (an antibody which initiates the natural God given immune response) within the respiratory tract mucosa. Bypassing this mucosal aspect of the immune system by directly injecting organisms into the bloodstream leads to a corruption in the immune system itself. As a result, the pathogenic viruses or bacteria cannot be eliminated by the immune system and remain in the body, where they will further grow and/or mutate as the individual is exposed to ever more antigens and toxins in the environment which continue to assault the immune system.

The mechanism by which the immune system is corrupted can best be realized when you understand that the two poles of the immune system (the cellular and humoral mechanisms) have a reciprocal relationship. Thus, when one is stimulated, the other is inhibited. Since vaccines activate the B cells to secrete antibody, the T cells are subsequently suppressed. This suppression of the cell mediated response is a key factor in the development of cancer and life threatening infections. In fact, the “prevention” of a disease via vaccination is, in reality, an inability to expel organisms due to the suppression of the cell-mediated response. Thus, rather than preventing disease; they actually prevent the disease from ever being resolved. The organisms continue circulating through the body, mutating and transforming into other organisms (as demonstrated by the work of Professor Antoine Bechamp), depending on the acidity and toxicity of the internal terrain of the body. Note that Bechamp proved that Louis Pasteur’s “germ theory” of disease was incorrect due to this ability of organisms to transform and mutate based on the body’s internal terrain (as Pasteur admitted on his deathbed). Thus, treatment of infection with antibiotics as well as “prevention” of disease with vaccines are both just examples of cutting off the branches of dis-ease, when the root of the cause is a toxic internal environment. However, since Pasteur’s germ theory was conducive to the profits of the burgeoning pharmaceutical companies who only manage dis-ease, no mention of the work of Professor Bechamp has been made in medical school curricula.

To make matters worse than the suppression of cellular immunity which occurs when vaccines are injected, adjuvants (which are substances added to vaccines to enhance the antibody response) can actually lead to serious side effects themselves. Adjuvants include oil emulsions, mineral compounds (which may contain the heavy metal aluminum), bacterial products, liposomes (which allow delayed release of substances), and squalene. The side effects of adjuvants themselves include hyperactivity of B cells leading to pathologic levels of antibody production, as well as allergic reaction to the adjuvants themselves (as demonstrated in Gulf War I soldiers injected with vaccines containing the adjuvant squalene, to which antibodies were found in many soldiers). Note that the pathologically elevated hyperactivity of antibody production caused by adjuvants also results in a distraction from the other antigens that the immune system encounters “naturally”, which must be addressed to maintain health.

This hyperactivity of the humoral (antibody producing) pole of the immune system is, in this author’s opinion, the sole cause of all autoimmune diseases. The only thing which determines which autoimmune disease you develop is which tissues in your body are attacked by auto-antibodies. If the inside lining of the gastrointestinal tract (the mucosa) is attacked by auto-antibodies you develop leaky gut syndrome (which leads to food allergies when partially digested food particles are released into the bloodstream, are recognized as antigens foreign to the body, and elicit an antibody response against those food particles that becomes heightened every time that same food is eaten and released into the bloodstream partially digested again). Crohn’s disease and colitis are also caused by auto-antibody attack on the mucosa of the GI tract itself. If the islet (insulin producing) cells of the pancreas are attacked by auto-antibodies, you develop insulin dependent (juvenile) diabetes. If the respiratory mucosa is attacked by auto-antibodies, you develop “leaky lung” syndrome where, just as with leaky gut, antigens recognized as foreign to the body which are inhaled are able to traverse the lining of the respiratory tract, causing the creation of antibodies against those antigens (usually dust, mold, pet or pollen antigens). When these substances are inhaled again, the allergic response producing constriction of the bronchioles is called asthma. If the components of the articular surface of the joints are attacked by auto-antibodies, you develop rheumatoid (or juvenile) arthritis. If the skin is attacked, you develop “leaky skin” syndrome, where contact antigens which could not otherwise traverse the skin are allowed in, leading to skin allergies to contact antigens. Additionally, depending on which level of the skin is attacked by auto-antibodies, (i.e., the epidermis or dermis), you develop eczema, psoriasis or scleroderma. If the kidney tissue is attacked by auto-antibodies, you develop one of the many types of nephritis, depending on which component of renal tissue is attacked (for example, with glomerulonephritis, the basement membrane of the glomerular apparatus within the kidney (which filters blood to form urine) is attacked by auto-antibodies, thus allowing protein to escape from the serum into the urine). If you develop auto-antibodies against thyroid gland tissue, you develop Grave’s disease. If you develop auto-antibodies against the tissue of the thymus gland (which is crucial in T cell production and function), you develop myasthenia gravis. If you develop auto-antibodies against the very DNA in the nucleus of all cells, you develop systemic Lupus (thus, the potential autoimmune potential of DNA vaccines being developed now is self evident; worse yet, DNA components from these vaccines can be incorporated into your DNA, leading to actual genetic changes which could cause extinction of all (vaccinated) life on the Earth). And on, and on, and on.

The brain and spinal cord can also be attacked with auto-antibodies (which this author refers to as vaccine induced encephalitis), leading to a variety of neurological diseases. The most severe of these, leading to death, are sudden infant death syndrome (SIDS) and most cases of “shaken baby syndrome”. If components of the myelin sheath (the insulating covering of nerve fibers which allows proper nerve conduction) or the actual neurofilaments themselves are attacked by auto-antibodies, the resultant condition is determined solely by the location of the damage done. Such neurological conditions include but are not limited to minimal brain dysfunction, ADD/ADHD, learning disabilities, mental retardation, criminal behavior, the spectrum of pervasive developmental disorders (including autism), multiple sclerosis, Parkinson’s, Lou Gehrig’s disease, Guillen Barre,, seizure disorders, etc., etc. etc. (Please note that other toxins are also sometimes involved, such as: aspartame, Lymes and mercury in cases of MS; aspartame in seizures; or pesticides in cases of Parkinson’s). Thus, when detoxing to reverse these diseases, these other substances must also be detoxed to obtain a full recovery. However, the corruption of the immune system caused by the injection of vaccines is a key component in these disease states leading to immune malfunction, and is the reason why an autistic child may also have leaky gut or eczema, etc. Note that myelin production, for the most part, does not begin until after birth. Most myelin is apparently laid down by age 5 years and usually completed by age 10 years, judging by the level of success at various ages in reversing autistic and other neurological VIDS symptoms that this author has observed in hundreds of children by detoxing the viruses with homeopathic nosodes, and repairing the immune corruption by simultaneous administration of bovine colostrum (i.e., after 10 years of age, the ability to stop and repair auto-antibody induced damage in the myelin sheath and neurofilaments themselves is dramatically decreased).

Thus, the hyperactivity of the humoral arm of the immune system in autoimmune disease is caused by adjuvants added just for that purpose. However, the autoimmunity itself (i.e., antibody against self) has several mechanisms, including the following:

1. The antigens present in the culture media itself cannot be completely filtered and separated from the organisms cultured thereon. Thus, any antibodies formed against antigens from the culture cells themselves (for example myelin basic protein from chick embryos or the 13 vaccines which now contain aborted fetal cells) can cross-react to form an autoimmune reaction against the myelin basic protein in your myelin sheath, etc.

2. Molecular mimicry is due to similarity of proteins contained in organisms and mammals. (For example, the measles virus is made up of proteins similar to myelin basic protein; thus, antibodies formed against the measles virus antigens subsequently also cause an auto-antibody attack against myelin basic protein in the myelin sheath due to cross reactivity of these antibodies).

3. intentional inclusion of antigens in vaccines to cause formation of antibodies that attack specific hormones or races (for example, experiments done on women of childbearing age in the Philippines and probably other locations where HCG (human chorionic gonadotropin, the hormone produced when women first become pregnant) placed into vaccines given these women resulted in antibodies against the HCG hormone, and subsequent spontaneous abortion thus occurred when the women became pregnant. It is also this author’s hypothesis that the epidemic of vitiligo in people of color (hypo pigmentation of skin caused by auto-antibody attack on melanocytes (melanin producing cells) in skin) is also occurring due to intentional inclusion of melanin in vaccines given to people of color.

In addition to the above phenomena which lead to simultaneous depression of cellular immune function and hyperactivity of humoral immune function, vaccines also contain other toxic substances which can cause serious side effects themselves. The following ingredients are actually listed on the CDC website with this introductory statement: “Many things in today’s world, including food and medicines, have chemicals added to them to prevent the growth of germs and reduce spoilage.” Translation: you,re already toxic, so what’s the big deal with adding more poison? This author’s answer to that question is that any immunotoxin can end up being the “straw that breaks the immune system’s back” in that individual, leading to dis-ease. This is where genetics is key; i.e., not that what disease you develop is actually caused by some “gene” in most cases; but rather that your genes determine the strength of your immune system (i.e., how many assaults your immune system can take before it reaches critical mass, and you develop a dis-ease).

Some additional ingredients in vaccines (as listed by the CDC on their website) include antibiotics, aluminum gels, formaldehyde, monosodium glutamate (MSG), egg protein, and sulfites. Thus, we have antibiotics (which you could be allergic to); aluminum (highly involved in causing Alzheimer’s disease); formaldehyde (a toxic carcinogenic substance used to pickle dead people); MSG ( a potent excitotoxin which, like aspartame, can cause seizures, brain tumors, etc.); egg protein (to which you could have a life threatening anaphylactic reaction); and sulfites (another toxin which we are advised not to consume much of orally, but in vaccines, it is injected directly into the blood stream). Is this not a veritable witch’s brew of chemicals, organisms, and animal or human (aborted fetus) body parts? Note in this list that they do not mention the ethyl-mercury containing preservative thimerosol, which has been the only dangerous substance in vaccines to receive mainstream media attention (albeit most of that being disinformation) after the explosion in the rate of occurrence of autism in the last generation became self-evident proof that vaccines are the causative factor. For, although the scientists working for the medical mafia continue to use statistics to twist and spin their data to make us beLIEve that vaccines are not the cause, too many thousands of parents have watched their children enter the downward spiral into autism after their children received the vaccine which was the straw that broke the back of their child’s immune system. No matter what the “white coats” tell these parents; they know the truth!

Mercury (also in dental amalgam fillings) is a highly toxic heavy metal, has been documented to cause cancer, and can be absorbed through the digestive track, skin, and respiratory track. Mercury is 1,000 times more toxic than lead, and is second only to uranium as the most toxic metal. If children receive all recommended vaccines, they will receive 2,370 times the “allowable safe limit” for mercury in the first two years of life (as if there is such a thing as a “safe” amount of a toxic poison). Yet, even after Congressional hearings instigated by Congressman Dan Burton (whose own grandchild became autistic after receiving vaccines) resulted in the FDA requesting (not ordering) vaccine manufacturers to remove this toxic heavy metal from their products, mercury is still present in many vaccines.

Although the symptoms of mercury poisoning are identical to the symptoms of autism, it should be noted that most children who descend into the hellish state known as autism do so after the MMR vaccine. The MMR vaccine is one of the few vaccines that do not contain mercury. Thus, it is self-evident that the removal of mercury will not make vaccines “safe”. (This is why the mercury is the only thing being addressed at all; because when the people reading this paper realize that the very mechanism by which vaccines corrupt the immune system means that NO vaccine is safe and effective; there will be an evolution of consciousness where the structure of lies telling us vaccines are safe and effective disintegrates.) In the autistic community, this will lead to an exodus from the multiple autism groups saying it is all about the mercury or worse yet, that autism genes are “inherited”, to the only group which has their focus on the actual problem. This group is named TAAP (the Autism Autoimmunity Project at http://www.taap.info/), and is led by April Oakes. In this author’s opinion, it will be TAAP in alliance with the vaccine damaged soldiers and vets of the American Gulf War Veterans Association at http://www.agwva.org led by Peter Kawaja which, working together, will stop this holocaust on humanity called VIDS. The good news is that these VIDS can be reversed using natural remedies contained in the Hippocrates Protocol (www.drcarley.com). This “surgical strike” detoxification approach which has the potential to reverse ALL of the aforementioned conditions under the VIDS umbrella as long as detoxification is started early enough (before age 10 for neurological VIDS) will be the one truth put on top of the mountain of lies (that vaccines are safe and effective) that will cause the entire mountain of vaccine lies to crumble. Combined with a massive outpouring of public support to these two organizations, the root of the tree of vaccine evil will be exposed. Thus, the holocaust on humanity (where instead of people being put in concentration camps, the concentration camps are being put into the people) will finally be put to an end.

Unfortunately, we can no longer pretend that this epidemic of VIDS is merely a “mistake” made by good intentioned, albeit misguided mad scientists. Because it’s even worse than the above, folkswe are talking TREASON and CRIMES AGAINST HUMANITY, PETS, and even PLANTS, (which are also being genetically modified to create vaccines). The evidence for this is as follows:

As concern for population growth started to grow and the final plans to bring in the New World Order were put in place, this lie called vaccines was transformed into pure evil, as it was realized that such delivery systems could be used to intentionally cause disease, which is now being done under the US Code, Title 50, Chapter 32, § 1520 and 1524. You can read it for yourself at your local library, or go to

http://www.drcarley.com/Title%2050%20US%20Code.htm.

This law has been in place since the 1960’s, and it was last modified in April of 2000. The only stipulation made for experimentation on human subjects is that local civilian officials be notified 30 days before the experiment is started. Section 1524 adds that the Secretary of Defense may enter into agreements with the Secretary of Health and Human Services to provide support for vaccination programs through use of excess peacetime biological weapons (i.e., weapons of mass destruction). In April 2000, § 1520 (a) was passed to put alleged restrictions on the use of human subjects for testing of chemical or biological agents after a caller on C Span mentioned this law in 1999, which revealed this treasonous law to a huge audience of listeners (including this author, who has been including it in lectures and written materials since that call came into “Washington Journal”). However, the exceptions written to Title 50, chapter 32 under § 1520 subsection (b) in the 2000 law passed by our aiders and abettors of treason in Congress not only loophole back in a test carried out for “any peaceful purpose that is related to a medical, therapeutic, pharmaceutical, agricultural, industrial, or research activity”; but add that such biological and chemical warfare agents can now be also used for any law enforcement purpose, including “any purpose related to riot control” (just in case those C Span listeners should actually get off the couch at the horror of what the traitors in Washington, D.C. are doing to God’s people). Subsection (c) of this law now mandates that “informed consent” be required. In reality, not a single vaccine has ever been tested for its long term side effects (including carcinogenic potential). Additionally, the intentional introduction of stealth viruses, (including man-made viruses that cause cancer, mycoplasma and the HIV virus), antigens which target certain races, (and surely a microchip in the future) into vaccines makes it self evident that informed consent is impossible, as it would initiate impeachment proceedings and war crimes trials against every “public servant” involved in perpetrating these crimes against the American people, in violation of the Nuremberg Code (which was written after the end of WW II to prevent the barbaric experiments that occurred in the Nazi concentration camps) .

What most people don’t know is that the top level mad scientists from Nazi Germany were actually brought to the United States through “Operation Paperclip”, and have been continuing their work to this day in places like Brookhaven labs, Cold Spring Harbor and Plum Island in this author’s backyard on Long Island. (To see the document proving that American scientists created the HIV virus, this author refers you to p. 442 of Death in the Air by Dr. Leonard G. Horowitz, where you can read the 1969 document in which the U.S. military/CIA and Rockefeller directed National Academy of Sciences-National Research Council (NAS-NRC) announced that a research program to explore the feasibility of “creating a new infective microorganismwhich would be refractory to the immunological and therapeutic processes upon which we depend to maintain our relative freedom from infectious disease” could be completed at a total cost of $10 million.) Yes, this is what your tax dollars are going towards, folks. But hang on to your hat, because it only gets worse.

The most heinous, bone chilling and evil piece of this puzzle has been revealed to the world by an American hero named Peter Kawaja, who worked in the late 1980’s as a security and counter terrorism expert for the United States government (a service for which he has been rewarded with the murder of his wife, torching of his home, issuance of a war crimes subpoena to (they thought) confiscate all his evidence, illegal IRS liens on all subsequent income, and multiple attempts on his own life, all funded by YOUR tax dollars). Please go to http://www.agwva.org/mission.htm and read some of the 34 counts that Mr. Kawaja brought against the domestic traitors to America (in both their individual and governmental capacities) in a federal lawsuit in which the perpetrators, again, used your tax dollars to hire themselves attorneys from the Department of “Justice” whose defense of their war criminal clients was that they are “immune, under color of law”. (You can listen to Mr. Kawaja on one of his multiple internet radio shows, including “What’s Ailing America?” which he co-hosts with this author at http://www.highway2health.net every Wednesday at 10 PM, EST.

Dr. James R. Shannon, former director of the National Institute of Health reported in December, 2003 that “the only safe vaccine is one that is never used”. However, the reverberating truth, “the shot heard round the world” which will lead to the evolution of consciousness necessary to stop the holocaust against humanity known as vaccinations, will be that not only are vaccinations not safe or effective, but that they are actually weapons of mass destruction being perpetrated upon humanity in the name of health, for the purpose of genocide and to bring in the New World Order. Part 2 of the genocidal plan could drop anytime with activation of the Model State Health Emergency Powers Act whenever the next fabricated terrorist attack using biological agents occurs. Worse yet, the Congressional traitors in Washington posing as public “servants” are doing all they can to pass “Codex” legislation which will make the natural remedies and supplements used in the Hippocrates Protocol developed by this author to reverse all dis-eases only available by prescription. So, you didn’t hear about that on your local news station either? Please go to the site of another American hero, John Hamill of the International Alliance for Health Freedom (who reversed his schizophrenia symptoms with these natural supplements and has dedicated his life to stop Codex from passing) at http://www.iahf.com .

Wake up, America-it’s getting very late. It is time for the mountain of lies to crumble. Please spread the world to everyone you know we can make it happen. The time to stop chopping at branches and get to the root of this evil is now.


Canada Plans to Vaccinate Entire Population

June 22, 2009
Sharon Kirkey
The Windsor Star
June 22, 2009

Five-to-40-year-olds and Canada’s aboriginal communities should be the first to get vaccinated against human swine flu, experts say as Canadian officials decide who gets priority for the flu shots.

Under Canada’s official pandemic plan, the entire population would ultimately be immunized against the H1N1 swine flu.

But the vaccine will become available in batches, meaning the entire population can’t be vaccinated at once. It might take four or five months to get all the vaccine we’re going to get, during which time a second wave of swine flu may well be underway.

The Public Health Agency of Canada is working on a priority list, deciding where the first batches should go, and who should get the injections first. All provinces and territories would be expected to follow the national prioritization scheme.

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