And here is the transcript of the interview with him:
http://www.whale.to/v/kalokerinos.html
If it is scientific evidence the vaccinators want this should be ample - specially when I have been looking in medical and scientific literature for 25 years for scientific evidence that vaccines are safe and effective - there isn’t any!
STORE THIS ON YOUR COMPUTER FOR READY REFERENCE. YOU CAN ’COPY AND PASTE’ ANY SECTION AND FIND RELATED MATTER ON THE INTERNET. SOMEONE HAS DONE A LOT OF WORK TO GET THIS INFORMATION TOGETHER.
THIS TYPE OF INFORMATION HAS NEVER BEEN READILY AVAILABLE TO THE GENERAL PUBLIC.
NOW IS YOUR CHANCE TO READ 40 YEARS OF RESEARCH ON VACCINATION.
THE DEBATE ABOUT VACCINES HAS BEEN GOING ON SINCE 1798.
READ THE OTHER SIDE OF THE STORY THAT YOU HAVE NOT BEEN TOLD ABOUT BY YOUR DOCTOR, GOVERNMENT OR MAINSTREAM MEDIA, WHO ARE ALL SUPPORTED BY BIG PHARMA IN ONE WAY OR ANOTHER.
Voluminous Research Proves Vaccines are Deadly
Doctors who explain clearly why vaccines aren’t safe or effective.
1. Dr. Nancy Banks - http://bit.ly/1Ip0aIm
2. Dr. Russell Blaylock - http://bit.ly/1BXxQZL
3. Dr. Shiv Chopra - http://bit.ly/1gdgh1s
4. Dr. Sherri Tenpenny - http://bit.ly/1MPVbjx
5. Dr. Suzanne Humphries - http://bit.ly/17sKDbf
6. Dr. Larry Palevsky - http://bit.ly/1LLEjf6
7. Dr. Toni Bark - http://bit.ly/1CYM9RB
8. Dr. Andrew Wakefield - http://bit.ly/1MuyNzo
9. Dr. Meryl Nass - http://bit.ly/1DGzJsc
10. Dr. Raymond Obomsawin - http://bit.ly/1G9ZXYl
11. Dr. Ghislaine Lanctot - http://bit.ly/1MrVeUL
12. Dr. Robert Rowen - http://bit.ly/1SIELeF
13. Dr. David Ayoub - http://bit.ly/1SIELve
14. Dr. Boyd Haley PhD - http://bit.ly/1KsdVby
15. Dr. Rashid Buttar - http://bit.ly/1gWOkL6
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17. Dr. Ken Stoller - http://bit.ly/1MPVqLI
18. Dr. Mayer Eisenstein - http://bit.ly/1LLEqHH
19. Dr. Frank Engley, PhD - http://bit.ly/1OHbLDI
20. Dr. David Davis - http://bit.ly/1gdgJwo
21. Dr. Tetyana Obukhanych - http://bit.ly/16Z7k6J
22. Dr. Harold E Buttram - http://bit.ly/1Kru6Df
23. Dr. Kelly Brogan - http://bit.ly/1D31pfQ
24. Dr. RC Tent - http://bit.ly/1MPVwmu
25. Dr. Rebecca Carley - http://bit.ly/K49F4d
26. Dr. Andrew Moulden - http://bit.ly/1fwzKJu
27. Dr. Jack Wolfson - http://bit.ly/1wtPHRA
28. Dr. Michael Elice - http://bit.ly/1KsdpKA
29. Dr. Terry Wahls - http://bit.ly/1gWOBhd
30. Dr. Stephanie Seneff - http://bit.ly/1OtWxAY
31. Dr. Paul Thomas - http://bit.ly/1DpeXPf
32. Many doctors talking at once - http://bit.ly/1MPVHOv
33. Dr. Richard Moskowitz - http://bit.ly/1OtWG7D
34. Dr. Jane Orient - http://bit.ly/1MXX7pb
35. Dr. Richard Deth - http://bit.ly/1GQDL10
36. Dr. Lucija Tomljenovic - http://bit.ly/1eqiPr5
37. Dr Chris Shaw - http://bit.ly/1IlGiBp
38. Dr. Susan McCreadie - http://bit.ly/1CqqN83
39. Dr. Mary Ann Block - http://bit.ly/1OHcyUX
40. Dr. David Brownstein - http://bit.ly/1EaHl9A
41. Dr. Jayne Donegan - http://bit.ly/1wOk4Zz
42. Dr. Troy Ross - http://bit.ly/1IlGlNH
43. Dr. Philip Incao - http://bit.ly/1ghE7sS
44. Dr. Joseph Mercola - http://bit.ly/18dE38I
45. Dr. Jeff Bradstreet - http://bit.ly/1MaX0cC
46. Dr. Robert Mendelson - http://bit.ly/1JpAEQr
Documentaries where hundreds of health professionals explain the extreme fraud and corruption behind vaccine propaganda. As you drive to work tomorrow and read the newspaper, notice that the truth about vaccines is purposely missing and that’s because it’s a war on the public, where the main weapon used to cull the herd is silencing the truth and providing massive rewards (both financial and psychological) to anyone willing to poison themselves and their own children. Quiet weapons for silent wars.
1. Vaccination - The Silent Epidemic - http://bit.ly/1vvQJ2W
2. The Greater Good - http://bit.ly/1icxh8j
3. Shots In The Dark - http://bit.ly/1ObtC8h
4. Vaccination The Hidden Truth - http://bit.ly/KEYDUh
5. Vaccine Nation - http://bit.ly/1iKNvpU
6. Vaccination - The Truth About Vaccines - http://bit.ly/1vlpwvU
7. Lethal Injection - http://bit.ly/1URN7BJ
8. Bought - http://bit.ly/1M7YSlr
9. Deadly Immunity - http://bit.ly/1KUg64Z
10. Autism - Made in the USA - http://bit.ly/1J8WQN5
11. Beyond Treason - http://bit.ly/1B7kmvt
12. Trace Amounts - http://bit.ly/1vAH3Hv
13. Why We Don’t Vaccinate - http://bit.ly/1KbXhuf
14. Autism Yesterday - http://bit.ly/1URU2A7
15. Denmark Documentary on HPV Vaccine - http://bit.ly/1AJI0dx
16. Vaxxed - bit.ly/1qackPC
17. Man Made Epidemic - http://bit.ly/1XsOi0R
18. 50 Cents A Dose - http://bit.ly/2c0h07P
19. Direct Orders - http://bit.ly/1ivShHg
20. Dtap - Vaccine Roulette http://bit.ly/2dBnc3u
21. Truthstream News: About All Those Vaccines - http://bit.ly/2gCMa4o
22. Hear The Silence - http://bit.ly/2g7NYpd
23. Cervical Cancer Vaccine - Is It Safe? - http://bit.ly/2h3Dvsh
24. Vaccines Revealed - https://www.vaccinesrevealed.com/free/
25. The Truth About Vaccines - http://bit.ly/2mX4Tyc
26. Vaccine Syndrome - http://bit.ly/2phXCKt
27. Injecting Aluminum - http://bit.ly/2qPkFwo
28. Manufactured Crisis: HPV, Hype & Horror - http://bit.ly/2qT0X3j
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 *** 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 *** 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 ***, 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.
http://www.theflucase.com/index.php?...mid=64&lang=en
4,250% Increase in Fetal Deaths Reported to VAERS After Flu Shot Given to Pregnant Women
Nov 23rd, 2012 | By Christina England
An increase of fetal deaths were reported to VAERS after pregnant women were given flu vaccines.
Documentation received from the National Coalition of Organized Women (NCOW) states that between 2009 and 2010 the mercury-laden combined flu vaccinations have increased Vaccine Adverse Events Reporting Systems (VAERS) fetal death reports by 4,250 percent in pregnant women. Eileen Dannemann, NCOW’s director, made abundantly clear that despite these figures being known to the Centers for Disease Control (CDC), the multiple-strain, inactivated flu vaccine containing mercury (Thimerosal) has once again been recommended to pregnant women as a safe vaccination this season.
Outraged by the CDC’s total disregard for human life, Ms. Dannemann accused the CDC of ’willful misconduct,’ saying that they are responsible for causing the deaths of thousands of unborn babies. She stated that the CDC deliberately misled the nation’s obstetricians and gynecologists and colluded with the American Journal of Obstetrics and Gynecology (AJOG) to mislead the public by advertising the flu vaccine as a safe vaccine for pregnant women when they knew fully well that it was causing a massive spike in fetal deaths.
In a letter to Dr. Joseph Mercola, Ms. Dannemann wrote:
“Not only did the CDC fail to disclose the spiraling spike in fetal death reports in real time during the 2009 pandemic season as to cut the fetal losses, but also we have documented by transcript Dr. Marie McCormick, chairperson of the Vaccine Safety Risk Assessment Working Group (VSRAWG) on September 3, 2010, denying any adverse events in the pregnant population during the 2009 Pandemic season.” [1]
HIDING LIFE-OR-DEATH EVIDENCE
Because the H1N1 pandemic vaccine had never been tested on the pregnant population, and to lessen the intensity of fears of the unknown risks, Dr. Marie McCormick of the CDC was employed to keep track of all adverse events during the 2009 pandemic season, including those adverse events in the pregnant population. Dr. McCormick was responsible for sending monthly reports to the Secretary of the Health and Human Services (HHS), citing any suspicious adverse events.
According to Ms. Dannemann, NCOW has been unable to obtain access to these monthly reports. After sending a Freedom of Information Act request to the CDC, she was told that she may have to wait 36 months to access what should be published public reports.
The Mercola letter continues:
“The Advisory Committee on Childhood Vaccines (ACCV) and CDC were confronted with the VAERS data from NCOW on September 3, 2010, in Washington, D.C., and then again by conference call on September 10, and then again in Atlanta, Georgia, on October 28, 2010. On both September 3 and September 10, Dr. Marie McCormick clearly denied that there were any adverse events for pregnant women from the 2009 flu vaccine.”
THE DOCTOR’S VERSION OF CONCEAL AND CARRY
To emphasize their point, on October 28, 2010, NCOW requested that Dr. Rene Tocco present their data at the CDC headquarters in Atlanta, Georgia. The CDC’s Dr. Shimabakuru gave a presentation on significant adverse reactions to the H1N1 vaccine, such as cases of Guillane-Barre Syndrome, which appeared to have risen three percent, claiming it as an insignificant signal.
No mention at all was made of adverse events related to pregnant women. Unfortunately for Dr. Shimabakuru, his attempts to pull the wool over the eyes of the audience were foiled when he was challenged by a member of the audience asking if the vaccine caused adverse events in pregnancy. Feeling cornered, he reluctantly looked in his bag and sheepishly presented a slide that corroborated the NCOW data, confirming that the CDC knew of the spike in fetal deaths in the fall of 2010. [2]
So, why did Dr. Shimabkauru have a slide containing compromising evidence in his bag? Why did he decide to hide the slide? Surely, if he had prepared a slide outlining this crucial data, it would have made sense to include the slide in his presentation. After all, a 4,250 percent increase in fetal deaths is far more significant that a three percent increase in Guillane-Barre Syndrome.
Ms. Dannemann believes that the existence of this slide, along with the omission of it in his presentation, confirms that the CDC knew of the spike in fetal deaths by the fall of 2010 and was attempting by any means possible not to make it public.
Outlining a catalog of events, Ms. Dannemann believes the CDC’s continual cover ups puts the lives of pregnant women and their unborn children in serious jeopardy. She maintained:
“Continuing the vaccine program without notifying the public or the healthcare practitioners of the VAERS miscarriage/stillbirth incoming data was clearly a purposeful decision. The CDC, aware of their own incoming stream of early vaccine adverse events reports, clearly decided to allow the obstetricians to continue, unwittingly, murdering and damaging the unborn so that the CDC’s blunder of recommending the double-dose vaccination of pregnant women could be kept under the radar.”
COLLABORATION AND CORRUPTION
Despite evidence that the CDC knew of the 4,250 percent increase in fetal death reports in 2009/2010, in order to ensure the continuance of the vaccine program for pregnant women, the CDC published a study in AJOG authored by Dr. Pedro Moro of the CDC in the fall of 2010. The study articulated that there were only 23 miscarriages caused by the single flu vaccine in 19 years between 1990 – 2009, an average of 1.2 miscarriages per year. This study formed the basis of a CDC worldwide publicity campaign that the flu shot was safe for pregnant women by willfully and strategically excluding the 2009 pandemic data, which was available to them. Ms. Dannemann said:
“Both the CDC and AJOG were well aware of the fact that physicians and the public were awaiting the results of the 2009 H1N1 untested vaccine on pregnant women, amid solid assurances to the public at the beginning of the pandemic season that the CDC was on top of collecting any adverse reactions to the vaccine by establishing the Vaccine Safety Risk Assessment Working Group chaired by Dr. Marie Mc Cormick (VSRAWG).”
Ms. Dannemann stated that by including the 2008/2009 flu season’s data but excluding the available 2009 data from the 2009/2010 flu season in the study published in AJOG, Dr. Moro was able to give the impression that the 2009/2010 pandemic season was covered in the data, which of course it was not. Ms. Dannemann believes that this was a deliberate act on his part because he was aware of the fetal death spike in the 2009/2010 data at the time of preparing the study and purposely excluded the 2009 pandemic data from the study to hide this fact.
In the fall of 2010, just in time for the new flu season, media outlets all over the world publicized the AJOG, peer-reviewed CDC/Dr. Moro study as adamant proof that the flu shot is safe for pregnant women. The NCOW documents prove at the same time as widely publicizing advice that all pregnant women required the combined flu vaccination, the CDC was busy organizing ten non-profit organizations, to sign a joint letter to urge obstetricians and gynecologists to continue to vaccinate their pregnant patients.
One of the organizations to sign the letter was The March of Dimes [3] who urged health care providers to recommend the flu vaccine to pregnant women and those who expect to become pregnant. They wrote the following recommendation to all medical professionals:
“Advice from a healthcare provider plays an important role in a pregnant and postpartum woman’s decision to get vaccinated against seasonal influenza. The American Academy of Family Physicians (AAFP), American Academy of Pediatrics (AAP), American College of Nurse-Midwives (ACNM), American College of Obstetricians and Gynecologists (The College), American Medical Association (AMA), American Nurses Association (ANA), American Pharmacists Association (APhA), Association of Women’s Health, Obstetric and Neonatal Nurses (AWHONN), March of Dimes, and Centers for Disease Control and Prevention (CDC) are asking for your help in urging your pregnant and postpartum patients to get vaccinated against seasonal influenza.
The Advisory Committee on Immunization Practices (ACIP) recommends that pregnant and postpartum women receive the seasonal influenza vaccine this year, even if they received 2009 H1N1 or seasonal influenza vaccine last year. Lack of awareness of the benefits of vaccination and concerns about vaccine safety are common barriers to influenza vaccination of pregnant and postpartum women.”
Representatives from all ten organizations signed the letter.
March of Dimes Document
WHAT THE CDC FAILED TO TELL PREGNANT MOMS
This year, on September 27, 2012, the Human and Environmental Toxicology Journal (HET) published Dr. Gary Goldman’s study that confirms NCOWs data, a 4,250 percent increase in the number of miscarriages and stillbirths reported to VAERS in the 2009/2010 flu season. [4] The study points out an astounding fact that no one saw until the publishing of the Goldman study in HET: the CDC had recommended the double-dosing of the pregnant population with the seasonal flu vaccine with mercury and the untested H1N1 vaccine with mercury.
In his abstract, Goldman said:
“The aim of this study was to compare the number of inactivated-influenza vaccine–related spontaneous abortion and stillbirth (SB) reports in the Vaccine Adverse Event Reporting System (VAERS) database during three consecutive flu seasons beginning 2008/2009 and assess the relative fetal death reports associated with the two-vaccine 2009/2010 season.”
The facts that Goldman exposed are extremely disturbing. He highlights the fact that the safety and effectiveness of the A-H1N1 had never been established in pregnant women and that the combination of two different influenza vaccines had never been tested on pregnant women at all.
Even more worrisome is the fact that the A-H1N1 vaccine inserts from the various manufacturers contained this warning:
“It is also not known whether these vaccines can cause fetal harm when administered to pregnant women or can affect reproduction capacity.”
Dr. Goldman also pointed out that the developing fetus is indirectly exposed to mercury when thimerosal-containing vaccines are administered to a pregnant woman. He outlined a study written by A.R. Gasset, M. Itoi, Y. Ischii and R.M. Ramer who examined what happened after rabbits were vaccinated with thimerosal–containing radioactive mercury. Goldman stated that from one hour post-injection to six hours post-injection, the level of radioactive mercury in the blood dropped over 75 percent. Yet from two hours post-injection to six hours post-injection, there were significantly increased radioactivity levels in the fetal brain, liver, and kidney.
Dr. Goldman concluded that because the rates of miscarriage reported to the Vaccine Adverse Events Reporting System (VAERS) for the single flu vaccine were relatively low, health care providers developed a false sense of security that flu vaccines administered during pregnancy were safe. Goldman explained that just because a single vaccine has been tested and considered to be relatively safe, this does not mean that vaccinating pregnant women with two or more Thimerosal containing vaccines will be safe for them or their unborn babies. Overall, Goldman firmly believes that the VAERS grossly underestimates the true rates of miscarriage and other adverse events encountered in the US population. Remember, it is estimated that less than a tenth of true adverse reactions are reported to the VAERS with a one percent reporting rate for serious adverse events, including death, according to a study led by former FDA Commissioner Dr. David A. Kessler. [5]
As seen in the Goldman study, with the return to a single flu shot, the flu vaccine-related reports of fetal loss have returned to a significantly lower level compared to the high level of fetal loss reports in the two-dose 2009/2010 flu season. However, higher than background flu shot vaccine-related fetal losses continue to be reported to the VAERS.
Furthermore, the Goldman study recommends that the babies who survived the deadly double dose in utero be monitored:
“In addition, because of the order of magnitude increase in fetal-loss report rates, from 6.8 fetal loss reports per million pregnant women vaccinated in the single-dose 2008/2009 season to 77.8 in the two-dose 2009/2010 season, further long term studies are needed to assess adverse outcomes in the surviving children. Additional research concerning potential synergistic risk factors associated with the administration of Thimerosal-containing vaccines is warranted, and the exposure-effect association should be verified in further toxicological and case-control studies.” (emphasis added)
Aside from fetal deaths, the CDC initiative to increase uptake of vaccines in pregnant women continues to fuel the increases in the levels of neurodevelopmental, developmental, behavioral abnormalities, and chronic illness in the surviving children. Due to omitting reports of fetal deaths, the CDC enjoys success in increasing the uptake and number of vaccines in the pregnant population. The Advisory Committee on Immunization Practices (ACIP) is now recommending not only the flu shot (with mercury) but also the Tdap vaccine.
CONCLUSION
The work of NCOW and Dr. Goldman has proven that potential lives are being destroyed before they are even old enough to draw their first breath. Developing fetuses who are fortunate enough to survive the onslaught of vaccinations now being recommended to pregnant women then need to play a form of Russian Roulette from the day they are born, because their caring parents followed the advice they were given by professionals who have been deliberately misguided.
Eileen Dannemann and her team have proven with their remarkable work that both public and professionals alike are being lied to and deceived by organizations put in place by the government to sanction our vaccination programs. In my opinion, this is genocide and the sooner people realize that all vaccines come with an element of risk and begin to research the dangers for themselves, the sooner these insane experiments will end.
Acknowledgements
We would like to thank Eileen Dannemann and Dr. Paul King for asking VacTruth.com to report on their very important work.
Eileen Dannemann is the director of the National Coalition of Organized Women and the founder of the student vaccine liberation Army www.VaccineLiberationArmy.com. Dr. Gary Goldman and Dr. Paul G. King, vaccine consultant to NCOW, have provided to the public a most important study.
References
Official transcript CDC’s Dr. Marie McCormick denies miscarriages, Sept. 3, 2010 ACCV. See page 37.
Influenza Vaccine Safety Monitoring (slide 20).CDC’s Dr. Tom Shimabukuro confirms NCOW data , Oct. 28, 2010 ACIP
Letter from March of Dimes, inlcuded in this article.
Dr Gary Goldman Comparison of VAERS fetal-loss reports during three consecutive influenza seasons: Was there a synergistic fetal toxicity associated with the two-vaccine 2009/2010 season? http://het.sagepub.com/content/early/2012/09/12/0960327112455067.abstract?rss=1 (abstract only)
Kessler, D.A. The Working Group. Natanblut, S. Kennedy, D. Lazar, E. Rheinstein, P. et al. Introducing MedWatch: A New Approach to Reporting Medication and Device Adverse Effects and Product Problems. JAMA 1993 June 2. 269 (21): 2765-2768.
http://vactruth.com/2012/11/23/flu-shot-spikes-fetal-death/
LIST OF VACCINE INGREDIENTS & THEIR KNOWN SIDE EFFECTS.
“Vaccine Side Effects”
There has been much recent concern regarding vaccines given to children, and their possible side effects. Particularly highlighted is the link between early childhood vaccines and autism. This article provides a list of known ingredients inside vaccines, and their documented side effects.
It will aid you in making informed decisions, which is something the industry is against. The corporations involved have attempted to suppress this information for decades. Readers are advised that there are extra chemicals and toxins which are not mentioned, because we based this list upon the ingredients which are public knowledge. If you know of anything we have missed, please contact us. It seems that the more we research this topic: the more sinister it becomes.
The connection to autism has already been repeatedly and scientifically established, and there are many other conditions caused by vaccines which are yet to be proven. Vaccines are said to prevent certain diseases. However, the chances of catching these diseases are incredibly remote, and the horrid side effects from vaccines are so common that vaccines cause much more harm than good. The chance that a particular vaccine will actually offer effective protection varies between 35% and 90%, and almost all of them expire. In some cases, vaccines will infect the patient with the very disease it is meant to offer protection from. Do you think they would do the right thing, and treat you for free.
Vaccine Ingredient: Aborted Human Fetus Tissue and Human Albumin
Did you ever wonder where aborted babies really went? Now you know. From a health perspective, the tissues from another human (not just animals) are still foreign, and therefore toxic to the body. One industry friendly web site matter-of-factly boasted, “The cells reproduce themselves, so there is no need to abort additional fetuses to sustain the culture supply. Viruses are collected from the diploid cell cultures and then processed further to produce the vaccine itself”. The Liberty Counsel reported, “You may be surprised to learn that some vaccinations are derived from aborted fetal tissue. Vaccines for chicken pox, Hepatitis A, and Rubella were produced solely from aborted fetal tissue”.
Vaccine Ingredient: Formaldehyde
This is used in vaccines as a tissue fixative, and a preservative. Formaldehyde is oxidized to become formic acid. Formic acid is the main ingredient of bee and ant venom. Concentrated, it is corrosive and an irritant. While absorbing the oxygen of the body, it may lead to acidosis, nerve, liver, and kidney damage.
According to the National Research Council, fewer than 20% but perhaps more than 10% of the general population may be susceptible to extreme formaldehyde toxicity, and may react to exposure at any level. Formaldehyde is ranked as one of the most hazardous compounds on ecosystems and human health, according to the Environmental Defense Fund. These findings are for environmental exposure, and therefore, the dangers are much greater for the formaldehyde included in vaccines, since it is injected directly into the blood.
The known side effects of formaldehyde are:
• Eye, nasal, throat and pulmonary irritation
• Acute sense of smell due to altered tissue proteins
• Anaemia
• Apathy
• Blindness
• Blood in urine
• Blurred vision
• Pain
• Bronchial spasms
• Bronchitis
• Burns in sinus area and throat
• Cardiac impairment
• Palpitations and arrhythmias
• Central nervous system depression
• Changes in higher cognitive functions
• Chemical sensitivity
• Chest pains and tightness
• Chronic vaginitis; colds
• Coma
• Conjunctivitis
• Constipation
• Convulsions
• Corneal erosion
• Death
• Destruction of red blood cells
• Depression
• Dermatitis
• Diarrhoea
• Difficulty concentrating
• Disorientation and dizziness
• Ear aches
• Eczema
• Emotional upsets
• Ethmoid polyps
• Fatigue
• Fecula bleeding
• Foetal asphyxiation
• Flu¬like or ’common cold’ illness
• Frequent urination with pain
• Gastritis
• Astrointestinal inflammation
• Headaches
• Haemolytic anaemia
• Haemolytic haematuria
• Hoarseness
• Hyperactive airway disease
• Hyperactivity
• Hypomenstrual syndrome
• Immune system (allergen) sensitizer
• Impaired (short) attention span
• Impaired capacity to attain attention
• Inability or difficulty swallowing
• Inability to recall words and names
• Inconsistent IQ profiles
• Inflammatory diseases of the reproductive organs
• Intestinal pain
• Intrinsic asthma
• Irritability
• Jaundice
• Joint pain
• Joint swelling
• Kidney pain
• Laryngeal spasm
• Loss of memory
• Loss of sense of smell
• Loss of taste
• Malaise
• Menstrual and testicular pain
• Menstrual irregularities
• Metallic taste
• Muscle spasms and cramps
• Nasal congestion
• Crusting and mucosa inflammation
• Nausea
• Nosebleeds
• Numbness and tingling ofthe forearms and finger tips
• Partial laryngeal paralysis
• Pneumonia,and Pulmonary Oedema
• Reduced bodytemperature
• Retarded speech pattern
• Ringing or tingling in the ear
• Schizophrenic¬ type symptoms
• Sensitivity to sound
• Shock
• Short term memory loss
• Shortness of breath
• Skin lesions
• Sneezing
• Sore throat
• Spacey feeling
• Speaking difficulty
• Sterility
• Swollen glands
• Tearing
• Excessive Thirst
• Tracheitis
• Tracheobronchitis
• Vertigo
• Vomiting blood
• Vomiting
• Wheezing and Lung Complication
Vaccine Ingredient: Mercury
Mercury compounds are used in vaccines as preservatives. The toxicity of mercury has been repeatedly ignored in the area of vaccines by the medical establishment and oversight agencies. Mercury is the second most poisonous element known to mankind (second only to uranium and its derivatives). Brain neurons rapidly and permanently disintegrate in the presence of mercury within 30 minutes of exposure. Mercury is also known to change a body’s chromosomes, so I especially worry about those who have had mercury ¬based dental fillings (which are the standard ’silver’ type), for these people are constantly being filled with this cumulative poison from the mercury’s vapors as well as direct contact inside the mouth.
The U.S. has known about the potential problems of Thimerosal (the preservative in vaccines that contains mercury) for many years. The World Health Organization voiced concerns about it in 1990.
Mercury is a cumulative poison, which means a body has difficultly removing it, and that levels of it in the body will grow significantly over time. Enormous amounts of mercury can accumulate over a lifetime. During a typical day of routine vaccines, infants sometimes receive the same amount of mercury as the absolute maximum set by the World Health Organization for 3 months of adult exposure.
The following was taken from a website affiliated with the National Institutes for Health detailing the effects of mercury exposure:
“Symptoms of high exposure to this class of mercury based compounds include: aphthous, stomatitis, satarrhal gingivitis, nausea, liquid stools, pain, liver disorders, injuries to the cardiovascular system and hematopoietic system, deafness and ataxia, death, headache, paresthesia of the tongue, lips, fingers and toes, other non¬specific dysfunctions, metallic taste, slight gastrointestinal disturbances, excessive flatus and diarrhea may occur.
Acute poisoning may cause gastrointestinal irritation and renal failure. Early signs of severe poisoning include fine tremors of extended hands, loss of side vision, slight loss of coordination in the eyes, speech, writing and gait, inability to stand or carry out voluntary movements, occasional muscle atrophy and flexure contractures, generalized myoclonic movements, difficulty understanding ordinary speech, irritability and bad temper progressing to mania, stupor, coma, mental retardation in children, skin irritation, blisters and dermatitis. Other symptoms include chorea, athetosis, tremors, convulsions, pain and numbness in the extremities, nephritis, salivation, loosening of the teeth, blue line on the gums, anxiety, mental depression, insomnia, hallucinations and central nervous system effects. Exposure may also cause irritation of the eyes, mucous membranes and upper respiratory tract.”
Complete intolerance to Thimerosal, the mercury containing preservative, is known to develop from previous vaccines. The vaccines stimulate the immune system and cause sensitization. The effects of mercury differ between inorganic, organic, and metallic mercury compounds. The neurologic toxicity symptoms caused by mercury compounds have a delayed onset after exposure, so few, if any of these symptoms will be noticed at the time of exposure. This explains the suspected long-term neurological symptoms of learning disabilities and behavior disorders associated with vaccines, which did not exist in previous generations.
Vaccine Ingredient: Antifreeze
Antifreeze (ethylene glycol) is an ingredient of the polio vaccine. It is classified as a “very toxic material”. It would take less than a tablespoonful to kill a 20¬pound dog with this substance. Pet owners are generally very wary around this dangerous substance, knowing that only a small amount is fatal. I can only imagine the effects that this has on the human body when directly injected into the blood stream.
Antifreeze can eventually lead to kidney, liver, blood and central nervous system (CNS) disorders. It is quite harmful and likely fatal if swallowed. Effects include behavioral disorders, drowsiness, vomiting, diarrhoea, visual disturbances, thirst, convulsions, cyanosis, rapid heart rate, CNS stimulation, depression, cardiopulmonary effects, kidney disorders. It can also lead to liver and blood disorders. It produces reproductive and developmental effects in experimental animals.
Vaccine Ingredient: Aluminium
Aluminum is a suspected carcinogen. It is a cardiovascular or blood toxicant, neurotoxicant, and respiratory toxicant. It has been implicated as a cause of brain damage, and is a suspected factor in Alzheimer’s Disease, dementia, convulsions, and comas. It has been placed on at least 2 federal regulatory lists.
Vaccine Ingredient: 2¬Phenoxyethanol
This is a suspected carcinogen. A developmental and reproductive toxicant. It is also a metabolic poison, which means that it interferes with the metabolism of all cells. This is the primary factor in the formation of cancer cells. It is capable of disabling the immune system’s primary response. It also contains phenol (see below for explanation).
Vaccine Ingredient: Phenol
This is a suspected carcinogen, and a cardiovascular and blood toxicant. Also known as carbolic acid; this is a developmental toxicant, gastrointestinal or liver toxicant, kidne toxicant, neurotoxicant, respiratory toxicant, skin and sense organ toxicant. It has been placed on at least 8 federal regulatory lists.
Vaccine Ingredient: Methanol
This is a volatile, flammable, poisonous liquid alcohol. In industry, it is used as a solvent, and an antifreeze compound in fuel. In the body it is metabolized into formaldehyde (as described earlier). Whilst it can be found naturally in the pectin that is present in some common fruits, the naturally occurring version is only in minute quantities, and the natural form is not known to cause harmful effects.
Vaccine Ingredient: Borax (sodium tetraborate decahydrate)
Traditionally used as a pesticide and ant killer. It is suspected to be a cardiovascular or blood toxicant, endocrin toxicant, gastrointestinal or liver toxicant, and neurological toxicant. It was found to cause reproductive damage and reduced fertility rates in studies on rats. It is already banned in foods in the United States, but astonishingly, it is still allowed for direct injection into the blood through vaccines. It is toxic to all cells, and has a slow excretion rate through the kidneys. Kidney retention and toxicity are the greatest. It has a cascading effect, causing liver degeneration, cerebral edema, and gastroenteritis.
“A single vaccine given to a 6 pound infant is the equivalent of giving a 180 lb. adult 30 vaccines in one day.”
Dr. Boyd Haley
Vaccine Ingredient: Glutaraldehyde
Glutaraldehyde is always toxic, causing severe eye, nose, throat and lung irritations, along with headaches, drowsiness, and dizziness. The effects mirror the chemical warfare agent known as nerve gas. It is poisonous if ingested, and known to cause birth defects in experimental animals. The effects of direct injection into the blood to bypass the process of ingestion are unknown. It is often used to clean medical equipment. In hospital accidents involving environmental exposure, it has been known to cause the following symptoms:
• Throat and lung irritation
• Asthma, asthma¬like symptoms, and breathing difficulty
• Nose irritation, sneezing, and wheezing
• Nosebleed
• Burning eyes and conjunctivitis
• Rash¬contact and/or allergic dermatitis
• Staining of the hands (brownish or tan)
• Hives
• Headaches
• Nausea
Vaccine Ingredient: MSG (Monosodium Glutamate)
Monosodium Glutamate is a synthetic flavor enhancer. In a 1995 report by the Federation of American Societies for Experimental Biology, two groups of people were defined as intolerant of MSG. This includes those who eat large quantitie of MSG (it is used in lots of processed foods as a flavor enhancer), and those with “poorly controlled asthma”. Our research indicates that anyone can suffer after consuming Monosodium Glutamate. In the 1995 report, which was contracted by the FDA, there was public admission that MSG yields the following symptoms:
• Burning sensations in the back of the neck, forearms and chest
• Numbness in the back of the neck, radiating to the arms and back
• Tingling, warmth, and weakness in the face, temples, upper back, neck and arms
• Facial pressure or tightness
• Chest pain
• Headache
• Nausea
• Rapid heartbeat
• Bronchospasm (difficulty breathing) in MSG ¬intolerant people with asthma
• Drowsiness
• Weakness
Note that this is the short¬list (the one with side effects the FDA actually admits), and it does not consider the highe toxicity of direct injection into the blood. The long list, which is about 15 times longer, includes heart attacks, especially in young people with magnesium deficiencies. Injections of glutamate in laboratory animals have resulted in rapid damage to nerve cells in the brain. MSG is in a special class of chemicals called excitotoxins, which are known to directly attack brain cells. In 1978, MSG was banned from baby foods and other baby products for infants who were less than one year of age, because the American Academy of Pediatrics and the National Academy of Sciences expressed concerns. It is now being used in these products again, along with vaccines.
Vaccine Ingredients: Sulfate and Phosphate Compounds
These can trigger severe allergies in children which may last throughout their lives to permanently impair their immune systems.
Vaccine Ingredient: Ammonium Sulfate
This is another carcinogen. Ammonium sulfate is prepared by mixing ammonia with sulfuric acid. It is used as a chemical fertilizer for alkaline soils to lower the pH of the soil. In the body, it stresses the immune system by causing acidosis. Ammonium sulfate is also a gastrointestinal (liver) toxicant, neurotoxicant, and respiratory toxicant.
Vaccine Ingredient: Gentamicin Sulfate
This is a strong antibiotic, which is often used for life¬ threatening illnesses (eg. pneumonia).
Known side effects:
• Muscle twitching
• Numbness
• Seizures
• Increased Blood Pressure
• Alopecia
• Purpura
• Pseudotumor cerebri
• Photosensitivity
• Transient irritation
• Burning
• Stinging
• Itching
• Inflammation
• Angioneurotic edema
• Urticaria
• Vesicular and maculopapular dermatitis
• Mydriasis
• Conjunctival paresthesia
• Conjunctival hyperemia
• Nonspecific conjunctivitis,
• Conjunctival epithelial defects
• Lid itching and swelling
• Bacterial/fungal corneal ulcers
Vaccine Ingredient: Neomycin Sulfate
When researching this, we discovered the neurotoxicity of neomycin sulfate following oral use as an antibiotic. I can only wonder about what damage this causes when injected directly into the blood of infants. It interferes with vitamin B6 absorption, which is the cause of a rare form of epilepsy, and mental retardation. Adult patients given neomycin as an antibiotic are typically placed under close clinical observation (ie. hospitalized), so that intensive care intervention is immediately available. Neurotoxicity has been reported, along with nephrotoxicity, and permanent bilateral auditory ototoxicity. Sometimes vestibular toxicity is present in patients with normal renal function when treated with higher or longer doses than recommended.
Vaccine Ingredient: Tri(n)butylphosphate
This is yet another carcinogen. This is a kidney toxicant and a neurotoxicant. It is more hazardous than most chemicals in 2 out of 3 ranking systems, on at least 1 federal regulatory list.
Vaccine Ingredient: Polymyxin B
This is another antibiotic. Injection of this is generally avoided by doctors (except in the case of vaccines), due to severe pain at injection sites, particularly in infants and children.
Other Known Side Effects:
• Albuminuria
• Cylindruria
• Azotemia
• Rising blood levels without any increase in dosage.
• Facial flushing
• Dizziness progressing to ataxia
• Drowsiness
• Peripheral paresthesias: circumoral and stocking¬glove
• Apnea
• Signs of meningeal irritation with intrathecal administration
Vaccine Ingredient: Polysorbate 20 /80 Emulsifier
This is a suspected carcinogen. It is a known skin and sense organ toxicant. It is verified as a cancer agent in animals.
Vaccine Ingredient: Sorbitol Sweetener
Diabetic retinopathy and neuropathy may be related to excess sorbitol in the cells of the eyes and nerves; leading to blindness. This is another suspected carcinogen. Sorbitol is a gastrointestinal and liver toxicant.
Vaccine Ingredient: Polyribosylribitol
This is an experimental artificial sweetener. Actually the experimentation is ongoing ? in children that is, without the knowledge or consent of their parents.
Vaccine Ingredient: Beta¬ Propiolactone
Documented as a verified carcinogen. It is a gastrointestinal (liver) toxicant, respiratory toxicant, skin toxicant, and sense organ toxicant. More hazardous than most chemicals; earning a 3 out of 3 in ranking systems. It appears on at least 5 federal regulatory lists. It is ranked as one of the most hazardous compounds to humans.
Vaccine Ingredient: Amphotericin B
This can cause irreversible kidney damage, and mild liver failure. It has been known to produce severe histamine (allergic) reactions. There are several reports of anemia and cardiac failure. According to the MME definition it is, “a drug used to treat fungus infections. Known allergy to this drug prohibits use. Side effects include blood clots, blood defects, kidney problems, nausea and fever. When used on the skin, allergic reactions can occur”.
Vaccine Ingredients: Animal Organ Tissue and Animal Blood
Animal cell lines are used to culture the viruses in vaccines, so animal tissues and impurities are included in the formulation that is injected. These tissues are unusable and toxic to the body except for when their protein materials are digested to form amino acids through normal food consumption. There is no digestion process for injections.
Injections may also contain many types of animal viruses (see the Animal Viruses section). Animals used include monkey (kidney), cow (heart), calf (serum), chicken (embryo and egg), duck (egg), pig (blood), sheep (blood), dog (kidney), horse (blood), rabbit (brain), guinea pig, etc.
Vaccine Ingredient: Large Foreign Proteins
In addition to the animal tissue impurities, there are large proteins that are deliberately included, and used for such purposes as adjuvants (substances that aggravate an immune response using their inherent toxicity). Egg album and gelatin (or gelatine, obtained from selected pieces of calf and cattle skins, de¬mineralized cattle bones and pork skin) are in several vaccines. Casein (milk protein) is in the triple antigen (DPT vaccine). When injected, these normally harmless proteins are toxic to the body. Hence the immune system “response”.
The immune system is intentionally stressed by this invasion to produce an unnatural sensitization to all the ingredients. The body will become further sensitive to these substances in the future, rather than becoming immune to them. So, the basic premise of vaccinations which the public has been sold is false. This explains why bizarre allergies such as lactose intolerance, egg, and nut allergies have suddenly become common in recent history.
Vaccine Ingredient: Latex
This is included in the hepatitis B vaccine which is given routinely to health workers. The high occurrence of the latex allergies among nurses is due to their sensitization to latex through the large amounts of chemical rubber which is injected into them. These vaccines produce a panicked immune response. These nurses will suffer with this allergy permanently. Such allergic reactions can be life ¬threatening.
This vaccine is now routinely given to newborn babies in many countries, including Australia, and the United States.
Vaccine Ingredient: Animal Viruses
Some of these can be particularly alien to the human body. The most frequently documented and publicised example is the monkey virus SV40. The virus is harmless in monkeys, but it stimulates rare cancers when injected into humans producing brain (tumors), bone (e.g. multiple myeloma), lungs (mesothelioma), and lymphoid tissue (lymphoma). Monkey Virus SV40 has only appeared in people born in the last 20 years (The Journal of Infectious Diseases, Sept. 1999), long after the manufacturer claimed to have “cleaned up” the polio vaccines where it was found. Such cases include the late Alexander Horwin, both of whose parents tested negative for SV40. Therefore, recent cases cannot just be blamed on inheritance from parents who received the vaccine (see www.ouralexander.org). This proves that manufacturers are secretly including it again.
Vaccine Ingredient: Human Viruses
The viruses against which the vaccine is supposed to protect are frequently said to be “killed”, “inactivated”, or “attenuated”. This is a myth. The main method used to inactivate viruses is treatment with formaldehyde, whose effectiveness is limited, and even then only temporary. Once the brew is injected into the body, the formaldehyde is broke down by the body potentially releasing the virus in its original state. This is intentional. It is documented in orthodox medical literature that these living “crippled” viruses can revert to their former virulence.
Please remember that the included viruses, and bacteria, which the vaccine is supposed to protect against are claimed to be in “very small doses”. These small doses are not small to the body, and these quantities are quite high enough for the diseases to occur. When they do occur, the cases are always severe, and sometimes fatal. Several deaths were reported in the British medical journal, Lancet, from vaccine ¬induced yellow fever.
A susceptible person may succumb to infection when exposed to only a minute doses, especially when it is injected directly into the bloodstream. Likewise, there are other cases in which a healthy person will not succumb, even when exposed to large doses environmentally. It is not the pathogens, but the interaction methods between pathogens and hosts which causes diseases to appear, and the level of their severity.
Vaccines may not manifest obvious injury, especially not immediately, but are still likely to cause long term harm to internal organs and the immune system given their ingredients, and their known effects.
Most disease symptoms are the visible signs of a body’s attempts to defend itself against the infection. With disease injections, many important defences in the digestion path and mucous membranes are bypassed.
Vaccine Ingredient: Mycoplasma
These are microscopic organisms lacking rigid cell walls and considered to be the smallest free¬living organisms. Many are pathogenic, and one species is the cause of mycoplasma pneumonia; which interestingly, is noted to occur only “in children and young adults”, according to Mosby’s Medical Dictionary. This is not simply in vaccines by accident. It is deliberately added as an adjuvant (to increase the immune system’s allergic “response”) to the vaccine. The ingredients must be either poisonous, or slightly biologically infectious to trigger immune system responses, in other words.
Vaccine Ingredient: Genetically Modified Yeast
This is in the Hepatitis B Vaccine. Given the controversy over the ingestion of genetically modified foods, how much more dangerous do you think the direct injection of them is? What are the future consequences of this genetic experimentation against our children? Normal yeast that grows throughout the tissues is already known to be the root cause of countless ailments which can last for years, and in the rare cases when it is proper diagnosed, these are called yeast infections. Yeast overgrowth directly attacks the immune system, and cripples the body’s ability to remove wastes, toxins, and absorb nutrients categorically. The standard treatment for it with antibiotics often actually strengthens these infections in the long-term by killing more of the beneficial flora which normally keeps yeast overgrowth in check.
Vaccine Ingredient: Foreign DNA
DNA is used from such organisms as animals, viruses, fungi, and bacteria. It has been documented that injecting foreign DNA can cause it, or a portion of it, to be incorporated into the recipient’s DNA. The horrendous long¬term multi-generational implications defy the imagination. Although, some people might actually find it beneficial to have their grandchildren born with three arms, or horns from the head. These possibilities may seem far-fetched, but with the rate at which these type of ingredients are being incorporated into vaccines, it is a matter of when they happen ? not if. Describing it as insane is being too gracious.
Prologue
The human body has never experienced such a direct invasion as this before. We hope that you consider this list, and the side effects of vaccines before giving your child vaccinations. We have strong reasons to believe that overall, and in general, that the risks of horrible and long¬ term side effects far outweighs the risks of the diseases which vaccines are supposed to prevent.
Human blood is supposed to be, and traditionally was, remarkably sterile. There were virtually no bacteria or organisms present in the bloodstream. With vaccines now being so prevalent, this is no longer the case. Contrary to what we have been told, they weaken the immune system dramatically instead of strengthening it. In the United States, the Hepatitis B Vaccine is given to a child on the day of his birth, often weakening his immune system for his lifetime. His small body is just becoming accustomed to the germs around him for the first time, and it needs the strong immune system that he was given to be intact.
Although vaccines are mandatory in the U.S., all states currently offer religious exemptions, and some states offer philosophical exemptions. You may wish to consider these as options in order to protect your children. Religious exemptions are quite appropriate for this, because you can tell them honestly, and with a straight¬ face, that you are doing it because it is the Christian thing to do.”
Dateline: Tuesday, 5th March 2019. Tonight I have a bee in my bonnet about the latest drug company propaganda and outright lies and I just need to vent.
My wife called me in to watch an SBS news presentation on the latest big pharma funded study from Denmark showing no link between the MMR vaccine and Autism. The person interviewed presented this as a complete statement of fact, incontrovertable. And then said it would not be likely to convince those who believed otherwise. Duh! Especially if you know it to be an untruth!
And nothing could be further from the truth! She is either a bald faced liar or completely ignorant on a topic she pretends to have expertise. Here is some data that will prove that point.
The Science is Settled? HARDLY!
Here is some data from the people who best know that most of what is presented to us as science is fiction created to support an agenda.
In 2005 Dr. John P.A. Ioannidis, currently a professor in disease prevention at Stanford University, published the most widely accessed article in the history of the Public Library of Science (PLoS) entitled Why Most Published Research Findings Are False.
In the report he states:
“There is increasing concern that most current published research findings are false.”
“It is simply no longer possible to believe much of the clinical research that is published, or to rely on the judgment of trusted physicians or authoritative medical guidelines. I take no pleasure in this conclusion, which I reached slowly and reluctantly over my two decades as an editor of the New England Journal of Medicine.” – Dr. Marcia Angell, a physician and longtime editor-in-chief of the New England Medical Journal (NEMJ).
“The case against science is straightforward: much of the scientific literature, perhaps half, may simply be untrue. Afflicted by studies with small sample sizes, tiny effects, invalid exploratory analyses, and flagrant conflicts of interest, together with an obsession for pursuing fashionable trends of dubious importance, science has taken a turn towards darkness.” – Dr. Richard Horton, the current editor-in-chief of the Lancet – considered to be one of the most well respected peer-reviewed medical journals in the world.
Vaccines Don’t Cause Autism. EXCEPT WHEN THEY DO!
Just this week I saw a Facebook post showing a link to a page that listed 157 studies proving the link between vaccines and autism.
“There is no science that shows vaccines cause autism” - EXCEPT in all these government (ironic, isn’t it?) published studies which show that vaccines do indeed cause autism (and other health issues):
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878266/
http://www.ncbi.nlm.nih.gov/pubmed/21623535
http://www.ncbi.nlm.nih.gov/pubmed/25377033
http://www.ncbi.nlm.nih.gov/pubmed/24995277
http://www.ncbi.nlm.nih.gov/pubmed/12145534
http://www.ncbi.nlm.nih.gov/pubmed/21058170
http://www.ncbi.nlm.nih.gov/pubmed/22099159
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/
http://www.ncbi.nlm.nih.gov/pubmed/17454560
http://www.ncbi.nlm.nih.gov/pubmed/19106436
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3774468/
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3697751
http://www.ncbi.nlm.nih.gov/pubmed/21299355
http://www.ncbi.nlm.nih.gov/pubmed/21907498
http://www.ncbi.nlm.nih.gov/pubmed/11339848
http://www.ncbi.nlm.nih.gov/pubmed/17674242
http://www.ncbi.nlm.nih.gov/pubmed/21993250
http://www.ncbi.nlm.nih.gov/pubmed/15780490
http://www.ncbi.nlm.nih.gov/pubmed/12933322
http://www.ncbi.nlm.nih.gov/pubmed/16870260
http://www.ncbi.nlm.nih.gov/pubmed/19043938
http://www.ncbi.nlm.nih.gov/pubmed/12142947
http://www.ncbi.nlm.nih.gov/pubmed/24675092
http://www.ncbi.nlm.nih.gov/pubmed/25198681
PLUS:
Here are 83 cases reviewed by lawyers:
https://digitalcommons.pace.edu/cgi/viewcontent.cgi?article=1681&context=pelr
If you ever need a lawyer:
http://www.mctlawyers.com/vaccine-injury/cases/
Here are 157 Research Papers Supporting Vaccine/Autism Causation compiled by Ginger Taylor, MS.
https://www.scribd.com/doc/220807175/157-Research-Papers-Supporting-the-Vaccine-Autism-Link
“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, interleukin-6 secretion dysregulation, 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 thioredo in regulation, mineral deficiencies, impairment of the opioid system, endocrine dysfunction, cellular apoptosis, and other disorders.”
Read this about Hannah Brusewitz case and how she was harmed by DTP
https://www.law.cornell.edu/supct/cert/09-152
A dose-response relationship between organic mercury exposure from thimerosal-containing vaccines and neurodevelopmental disorders.
http://www.ncbi.nlm.nih.gov/pubmed/25198681
Relative trends in hospitalizations and mortality among infants by the number of vaccine doses and age, based on the Vaccine Adverse Event Reporting System (VAERS), 1990-2010.
http://www.ncbi.nlm.nih.gov/pubmed/22531966
Measles outbreak in a vaccinated school population: epidemiology, chains of transmission and the role of vaccine failures.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1646939/
A positive association found between autism prevalence and childhood vaccination uptake across the U.S. population.
http://www.ncbi.nlm.nih.gov/pubmed/21623535
Hepatitis B vaccination of male neonates and autism diagnosis, NHIS 1997-2002.
http://www.ncbi.nlm.nih.gov/pubmed/21058170
Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism.
http://www.ncbi.nlm.nih.gov/pubmed/12145534
The plausibility of a role for mercury in the etiology of autism: a cellular perspective
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3173748/
Detection of RNA of Mumps Virus during an Outbreak in a Population with a High Level of Measles, Mumps, and Rubella Vaccine Coverage
http://jcm.asm.org/content/46/3/1101.long
A case series of children with apparent mercury toxic encephalopathies manifesting with clinical symptoms of regressive autistic disorders.
http://www.ncbi.nlm.nih.gov/pubmed/17454560
Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity.
http://www.ncbi.nlm.nih.gov/pubmed/23609067
FDA concludes vaccines cause Autism
https://getcancercure.com/fda-announce-that-dtap-vaccine-causes-autism/
...“the present study provides new epidemiological evidence supporting an association between increasing organic-Hg exposure from Thimerosal-containing childhood vaccines and the subsequent risk of an ASD diagnosis”...
A two-phase study evaluating the relationship between... Autism spectrum disorder (ASD) is defined by:
NCBI.NLM.NIH.GOV
More than one scientist has linked the aluminium in vaccines and autism. Here is a comprehensive article on the research:
https://jbhandleyblog.com/home/2018/4/1/international2018
Protect Your Child’s Health With Vaccinations! NOTHING COULD BE FURTHER FROM THE TRUTH!
Is infant immunization a risk factor for childhood asthma or allergy?
http://www.ncbi.nlm.nih.gov/pubmed/9345669
The more kids are vaccinated, the more they die! Infant mortality rates regressed against number of vaccine doses routinely given: Is there a biochemical or synergistic toxicity?
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170075/
Infection, vaccines and other environmental triggers of autoimmunity.
http://www.ncbi.nlm.nih.gov/pubmed/16126512
DTP with or after measles vaccination is associated with increased in-hospital mortality in Guinea-Bissau.
http://www.ncbi.nlm.nih.gov/pubmed/17092614#
Unvaccinated Children are Healthier
http://www.mednat.org/vaccini/dannivacc_study.pdf
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