VACCINE INGREDIENTS …AND THEIR CHEMICAL PROFILES

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    VACCINE INGREDIENTS …AND THEIR CHEMICAL PROFILES

    Compiled By Arthur M. Evangelista, a former FDA Investigator

     

    Posted: 28 May 2004

     

    VACCINE INGREDIENTS

    Source: 1997 Physicians’ Desk Reference
    Toll Free Numbers can be called to obtain product inserts.
    This is a representative, not a comprehensive, list of the various types of vaccines.

    Acel-Immune
    DTaP
    Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed
    Lederle Laboratories
    1-800-934-5556
    produced using formaldehyde, thimerosal, aluminum hydroxide, aluminum phosphate, polysorbate 80, gelatin (animal parts/bovine)

    Act HIB
    Haemophilus Influenzae Type B (Hib) Tetanus Toxoid Conjugate
    Connaught Laboratories
    1-800-822-2463
    produced using ammonium sulfate, formalin, sucrose, thimerosal
    medium: semi-synthetic

    Attenuvax
    Measles Virus Vaccine Live
    Merck & Co, Inc.
    1-800-672-6372
    produced using neomycin, sorbitol, hydrolized gelatin
    medium: chick embryo

    DPT
    Diphtheria and Tetanus Toxoids and Pertussis Vaccine Adsorbed
    SmithKline Beecham Pharmaceuticals
    1-800-366-8900 ext. 5231
    produced using aluminum phosphate, formaldehyde, ammonium sulfate, washed sheep red blood cells, glycerol, sodium chloride, thimerosal
    medium: porcine (pig) pancreatic hydrolysate of casein

    Energix-B
    Hepatitis B
    SmithKline Beecham Pharmaceuticals
    1-800-633-8900 ext. 5231
    produced using aluminum hydroxide, thimerosal
    medium: yeast (possibly 5% residual)

    Havrix
    Hepatitis A
    SmithKline Beecham Pharmaceuticals
    1-800-633-8900 ext. 5231
    produced using formalin, aluminum hydroxide, phenoxyethanol (antifreeze), polysorbate 20, residual MRC5 proteins (from medium)
    medium: human diploid cells (originating from human aborted fetal tissue)

    Biavax
    Rubella and Mumps Virus Vaccine Live
    Merck & Co, Inc.
    1-800-672-6372
    produced using neomycin, sorbitol, hydrolized gelatin
    medium: human diploid cells (originating from human aborted fetal tissue)

    HibTiter
    Haemophilus Influenzae Type B (Hib)
    Lederle Laboratories
    1-800-934-5556
    produced using polyribosylribitol, ammonium sulfate, thimerosal
    medium: chemically defined, yeast based

    Fluvirin
    Influenza Virus Vaccine
    Medeva Pharmaceuticals
    1-888-MEDEVA
    (716)274-5300
    produced using embryonic fluid (chicken egg), neomycin, polymyxin, thimerosal, betapropiolactone
    medium: embryonic fluid (chicken egg)

    FluShield
    Influenza Virus Vaccine, Trivalent, Types A&B
    Wyeth-Ayerst
    1-800-934-5556
    produced using gentamicin sulfate, formaldehyde, polysorbate 80, tri(n)butylphosphate, thimerosal
    medium: chick embryos

    IPOL
    Inactivated Polio Vaccine
    Connaught Laboratories
    1-800-822-2463
    produced using 3 types of polio virus, formaldehyde, phenoxyethanol (antifreeze), neomycin, streptomycin, polymyxin B
    medium: VERO cells, a continuous line of monkey kidney cells

    MMR
    Measles Mumps Rubella Live Virus Vaccine
    Merck & Co., Inc.
    1-800-672-6372 produced using sorbitol, neomycin, hydrolyzed gelatin
    mediums: M&M – chick embryo
    Rubella – human diploid cells (originating from human aborted fetal tissue)

    M-R-Vax
    Measles and Rubella Virus Vaccine Live
    Merck & Co., Inc.
    1-800-672-6372
    produced using neomycin, sorbitol, hydrolyzed gelatin
    mediums: M – chick embryo
    R – human diploid cells (originating from human aborted fetal tissue)

    Menomune
    Meningococcal Polysaccharide Vaccine
    Connaught Laboratories
    1-800-822-2463
    produced using thimerosal, lactose
    medium: freeze dried polysaccharride antigens from Neisseria Meningitidis

    Meruvax II
    Rubella Virus Vaccine Live
    Merck & Co., Inc.
    1-800-672-6372
    produced using neomycin, sorbitol, hydrolyzed gelatin
    medium: human diploid cells (originating from human aborted fetal tissue)

    Mumpsvax
    Mumps Virus Vaccine Live
    Merck & Co., Inc.
    1-800-672-6372
    produced using neomycin, sorbitol, hydrolyzed gelatin
    medium: human diploid cells (originating from human aborted fetal tissue)

    Orimune
    Poliovirus Vaccine Live Oral Trivalent
    Lederle Laboratories
    1-800-934-5556
    produced using 3 types of attenuated polioviruses, streptomycin, neomycin, calf serum, sorbitol
    medium: monkey kidney cell culture

    Pneumovax
    Pneumococcal Vaccine Polyvalent
    Merck & Co., Inc.
    1-800-672-6372
    produced using phenol and capsular polysaccharides from the 23 most prevalent pneumococcal types

    Imovax
    Rabies Vaccine Adsorbed
    Connaught Laboratories
    1-800-822-2463
    produced using human albumin, neomycin sulfate, phenol red indicator
    medium: human diploid cells (originating from human aborted fetal tissue)

    Rabies Vaccine Adsorbed
    SmithKline Beecham Pharmaceuticals
    1-800-366-8900 ext. 5231
    produced using betapropiolactone, aluminum phosphate, sodium ethylmercurithiosalicylate (thimerosal), phenol red
    medium: fetal rhesus monkey lung cells

    Recombivax
    Hepatitis B Vaccine Recombinant
    Merck & Co., Inc.
    1-800-672-6372
    produced using thimerosal, aluminum hydroxide
    medium: yeast (residual < 1% yeast protein)

    RotaShield
    Rotavirus Vaccine, Live, Oral, Tetravalent
    Wyeth-Ayerst Laboratories
    1-800-934-5556
    produced using 1 rhesus monkey rotavirus, 3 rhesus-human reassortant viruses, sucrose, monosodium glutamate (MSG), potassium monophosphate, potassium diphosphate, fetal bovine serum, neomycin sulfate, amphotericin B
    medium: fetal rhesus diploid cell line

    Varivax
    Varicella Virus Vaccine Live
    Merck & Co., Inc.
    1-800-672-6372
    produced using sucrose, phosphate, glutamate, processed gelatin
    medium: human diploid cells (originating from human aborted fetal tissue)

     

    Chemical Profiles and Definitions

    visit http://www.scorecard.org/ to investigate chemical profiles
    Sources: EDF (Environmental Defense Fund) & MME (Mosby’s Medical Encyclopedia)

    Ammonium Sulfate: EDF Suspected – gastrointestinal or liver toxicant, neurotoxicant, respiratory toxicant

    Amphotericin B: MME definintion – “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.”

    Aluminum: EDF Suspected – cardiovascular, or blood toxicant, neurotoxicant, respiratory toxicant.
    More hazardous than most chemicals in 2 out of 6 ranking systems.
    On at least 2 federal regulatory lists.

    Beta-Propiolactone: EDF Recognized – carcinogen
    EDF Suspected – gastrointestinal or liver toxicant; respiratory toxicant; skin or sense organ toxicant.
    More hazardous than most chemicals in 3 out of 3 ranking systems.
    On at least 5 federal regulatory lists ranked as one of the most hazardous compounds (worst 10%) to humans.

    Formaldehyde: EDF Recognized – carcinogen
    Suspected – gastrointestinal or liver toxicant; immunotoxicant, neurotoxicant, reproductive toxicant; respiratory toxicant; skin or sense organ toxicant.
    More hazardous than most chemicals in 5 out of 12 ranking systems.
    On at least 8 federal regulatory lists ranked as one of the most hazardous compounds (worst 10%) to ecosystems and human health.

    Gentamicin Sulfate: an antibiotic

    Hydrolyzed Gelatin: obtained from selected pieces of calf and cattle skins, de-mineralized cattle bones (ossein) and porkskin.

    Neomycin: an antibiotic

    Phenol : EDF Suspected – cardiovascular or blood toxicant aka Carbolic Acid – developmental toxicant, gastrointestinal or liver toxicant kidney toxicant, neurotoxicant respiratory toxicant, skin or sense organ toxicant.
    More hazardous than most chemicals in 3 out of 10 ranking systems.
    On at least 8 federal regulatory lists.

    Phenoxyethanol: EDF Suspected – developmental toxicant, reproductive toxicant (aka: Antifreeze).
    Less hazardous than most chemicals in 3 ranking systems.

    Polyribosylribitol: a component of the Hib bacterium

    Polymyxin: an antibiotic

    Polysorbate: EDF Suspected – skin or sense organ toxicant

    Sorbitol: EDF Suspected – gastrointestinal or liver toxicant.
    Less hazardous than most chemicals in 1 ranking system.

    Streptomycin: an antibiotic

    Sucrose: refined sugar

    Thimerosal: EDF Recognized – developmental toxicant. Suspected – skin or sense organ toxicant.

    Tri(n)butylphosphate: EDF Suspected – kidney toxicant neurotoxicant.
    More hazardous than most chemicals in 2 out of 3 ranking systems.
    On at least 1 federal regulatory list.

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    #192
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    VACCINE INGREDIENTS and TOXIC EFFECTS AND MATERIALS

    List Of Toxic Materials
    Including BSE– In Vaccines

    Toxic Materials Put Into The Body With Vaccines

     

    Among these many toxic and/or contaminated ingredients is the now infamous Thimerosal (MERCURY). Also, casein and gelatin are bovine products. And how about those ‘washed sheep red blood cells’ in DPT…sheep have had ‘mad sheep’ disease (scrapie) for many decades.

    Note – READ the vaccine ingredients list below carefully. Do you want these items injected into your and your children’s bodies? Among these many toxic and/or contaminated ingredients is the now infamous Thimerosal (MERCURY). Also, casein and gelatin are bovine products. And how about those ‘washed sheep red blood cells’ in DPT…sheep have had ‘mad sheep’ disease (scrapie) for many decades. Do you feel lucky? – Jeff

     

    Polio – DPT contains:

    DPT – Diptheria and Tetanus Toxoids and Pertussis Vaccine Adsorbed

    SmithKline Beecham Pharmeceuticals 800-366-8900 x5231

    Produced using aluminum phosphate, formaldehyde, ammonium sulfate,

    washed sheep red blood cells, glycerol, sodium chloride, thimerosal

    medium: porcine (PIG) pancreatic hydrolsate of casein.

     

    Here is a more thorough list. Note the anthrax vaccine and its contents, including bovine material. Now wonder the vets got Gulf War Syndrome.

     

    Acel-Immune

    DTaP

    Diptheria and Tetanus Toxoids Acellular Pertussis Vaccine adsorbed

    Lederle Laboratories 800-934-5556

    Produced using formaldehyde, thimerosal, aluminum hydroxide, aluminum phosphate, polysorbate 80, gelatin.

     

    Act HIB

    Heamophilus Influenzae Type B (HIB) Tetanus Toxoid Conjugate

    Connaught Laboratories 800-822-2463

    Produced using neomycin, sorbitol, hydrolized gelatin

    Medium: chick embryo.

     

    DPT

    Diptheria and Tetanus Toxoids and Pertussis Vaccine Adsorbed

    SmithKline Beecham Pharmeceuticals 800-366-8900 x5231

    Produced using aluminum phosphate, formaldehyde, ammonium sulfate,

    washed sheep red blood cells, glycerol, sodium chloride, thimerosal.

    Medium: porcine (pig) pancreatic hydrolsate of casein.

     

    Hepatitis B

    SmithKline Beecham Pharmaceuticals 800-633-8900 x5231

    Produced using aluminum hydroxide, thimerosal.

    Medium: yeast (possibly 5% residual).

     

    IPOL

    Inactivated Polio Vaccine

    Connought Laboratories 1-800-822-2463

    Produced using 3 types of polio virus, formaldehyde, phenoxyethanol

    (antifreeze), neomycin, streptomycin, polymixin B.

    Medium: VERO cells, a continuous line of Monkey kidney cells.

     

    MMR

    Measles Mumps Rubella Live Viruse Vaccine

    Merck & Co., Inc. 800-934-5556

    Produced using sorbitol, neomycin, hydrolized gelatin.

    Mediums: M&M – chick embryo.

    Rubella – Human diploid cells (originating from human aborted fetal tissue).

    Produced using sorbitol, neomycin, hydrolized gelatin. -Mediums: M&M – chick embryo. Rubella – Human diploid cells (originating from human aborted fetal tissue).

     

    Orimune

    Poliovirus Vaccine Live Oral Trivalent

    Lederle Laboratories 800-934-5556

    Produced using 3 types of attenuated polioviruses, streptomycin,

    neomycin, calf serum, sorbitol.

    Meduim: monkey kidney cell culture

     

    Varivax

    Varicella Virus Vaccine Live (chicken pox Vaccine)

    Merck & Co., Inc. 800-672-6372

    Produced using sucrose, phosphate, glutamate, proceessed gelatin

    medium: Human Diploid Cells (originating from human aborted fetal tissue)

     

    Vaccines Grown In Aborted Fetal Cell Cultures

    Chickenpox, VARIVAX: Merck

    Hepatitis A, VAQTA: Merck

    Polio (oral), Poliovac, Canada: Connaught

    Polio, IMOVAX: Connaught

    Rabies, Imovax: Pasteur Merieux

    Rubella, MERUVAX: Merck

    Vaccines With Live Virus

    Chickenpox, VARIVAX: Merck

    Measles, ATTENUVAX: Merck

    Measles and Mumps, M-M-Vax: Merck

    Measles, Mumps and Rubella, M-M-RII: Merck

    Measles and Rubella, M-R-VaxII: Merck

    Mumps, MUMPSVAX: Merck

    Rubella, MERUVAX: Merck

    Rubella and Mumps: BIAVAX

    Hepatitis B: Merck

    Hepatitis B: SmithKline Beecham

    Lyme, LYMERIX: SmithKline Beecham

    RSV, Synapis: MedIMMUNE (vaccine or preventive treatment?)

    Vaccines With Animal And Cattle Parts

    Chickenpox, VARIVAX — fetal bovine serum: Merck

    Diphtheria, Tetanus, accelular Pertusssis, Acel-Immune — beef heart infusion: Lederle

    Infanrix — bovine extract: SmithKline Beecham

    Flu, FLUSHIELD — chick embryos: Wyeth: Fluzone — chicken embryos: Connaught

    Measles, ATTENUVAX — hydrolyzed gelatin: Merck

    Measles, Mumps and Rubella, M-M-RII — hydrolyzed gelatin: Merck

    Mumps, MuMPSVAX — hydrolyzed gelatin: Merck

    Polio, IPOL — calf serum, monkey kidney cells: Pasteur Merieux

    Polio (oral), ORIMUNE — kidney cells, calf serum: Lederle

    Rubella, MERUVAX — hydrolyzed gelatin: Merck

    Rubella and Mumps, BIAVAX — hydrolyzed gelatin: Merck

     

    Vaccines Using Cattle Material – (blood, fetal calf serum, meat broth–from

    countries U.S. government states have a RISK OF MAD COW DISEASES.)

    Anthrax: *BioPort DPT

    Certiva, Anthrax: *BioPort DPT

    Certiva, , diptheria, pertussis, tetanus: North American/Baxter International

    DPT: Infanrix, diptheria, pertussis, tetanus: GlaxoSmithKline Beecham

    Hep A: *Havrix, hepatitis A: GlaxoSmithKline Beecham

    Hib *ActHIB, haemophilus influenza Type B: Aventis Pasteur

    Hib: *OmniHIB: haemophilus influenza Type B: GlaxoSmithKline Beecham

    Pneumonia, *PNU-IMUNE 23: Lederle/American Home Products

    Polio IPOL: Aventis Pasteur

     

    * Cattle parts are NOT LISTED in vaccine package insert

     

    Illiniois Vaccine Awareness Coalition (IVAC)

    LIST OF TOXIC MATERIALS IN VACCINES
    There is an astonishing collection of poisons, toxic metals, chemical binders, and animal parts and juices in vaccines. You would not want to give this to your dog, yet it is routinely given to precious, little children.–Among these many toxic and contaminated ingredients is the infamous thimerosal, which contains mercury. Casein and gelatin are bovine products, and cattle are increasingly suspected of having CJD (mad cow disease). Keep in mind that we are here dealing with raw meat. It cannot be “cooked,” or the deadly viruses will be damaged. There are “washed sheep red blood cells” in DPT. Sheep in Britain and the U.S. have “mad sheep disease (scrapie). Reading the section on anthrax in the following list, it is little wonder that our troops in the Gulf War got “Gulf War Illness.”

    The diseases in vaccines are grown in the laboratory in monkey kidney cells, in human cells which may be cancerous, in chick embryo and in guinea pig cells. The cells are nourished with the blood serum from calves, which may be contaminated with numerous diseases such as bovine leukemia virus, bovine AIDS virus, or other animal diseases. Chemicals such as aluminum, formaldehyde (a human carcinogen) and MSG are used in processing of the vaccines. Thimerosal, a derivate of mercury and a deadly poison, is used as a preservative. These chemicals and potential diseases are all injected into your child’s body or your body as part of the vaccine.

    Acel-Immune DTaP Diphtheria and Tetanus Toxoids Acellular Pertussis Vaccine adsorbed Lederle Laboratories. Produced using formaldehyde, thimerosal, aluminum hydroxide, aluminum phosphate, polysorbate 80, gelatin.

    Act HIB Haemophilus Influenzae Type B (HIB) Tetanus Toxoid Conjugate Connaught Laboratories. Produced using ammonium sulfate, formalin, sucrose, thimerosal Medium: semi-synthetic.

    Attenuvax Measles Virus Vaccine Live Merck & Co, Inc. Produced using neomycin, sorbitol, hydrolized gelatin Medium: chick embryo.

    DPT Diphtheria and Tetanus Toxoids and Pertussis Vaccine Adsorbed SmithKline Beecham Pharmaceuticals. Produced using aluminum phosphate, formaldehyde, ammonium sulfate, washed sheep red blood cells, glycerol, sodium chloride, thimerosal. Medium: porcine (pig) pancreatic hydrolysate of casein.

    Hepatitis B SmithKline Beecham Pharmaceuticals. Produced using aluminum hydroxide, thimerosal. Medium: yeast (possibly 5% residual).

    IPOL Inactivated Polio Vaccine Connought Laboratories. Produced using 3 types of polio virus, formaldehyde, phenoxyethanol (antifreeze), neomycin, streptomycin, polymyixin B. Medium: VERO cells, a continuous line of Monkey kidney cells.

    MMR Measles Mumps Rubella Live Viruse Vaccine Merck & Co., Inc. Produced using sorbitol, neomycin, hydrolized gelatin. Mediums: M&M – chick embryo. Rubella – Human diploid cells (originating from human aborted fetal tissue).

    Orimune Poliovirus Vaccine Live Oral Trivalent Lederle Laboratories. Produced using 3 types of attenuated polioviruses, streptomycin, neomycin, calf serum, sorbitol. Meduim: monkey kidney cell culture.

    Varivax Varicella Virus Vaccine Live (chicken pox Vaccine) Merck & Co., Inc. Produced using sucrose, phosphate, glutamate, processed gelatin medium: Human Diploid Cells (originating from human aborted fetal tissue)

    Vaccines grown in aborted fetal cell cultures:

    Chicken pox (Varivax): Merck

    Hepatitis A (Vaqta): Merck

    Polio (oral) Poliovac, Canada: Connaught

    Polio (Imovax): Connaught

    Rabies (Imovax): Pasteur Merieux

    Rubella (Meruvax): Merck

    Vaccines with live virus

    Chicken pox (Varivax): Merck

    Measles (Attenuvax): Merck

    Measles and Mumps (M-M-Vax): Merck

    Measles, Mumps and Rubella (M-M-RII): Merck

    Measles and Rubella (M-R-VaxII): Merck

    Mumps (Mumpsvax): Merck

    Rubella (Meruvax): Merck

    Rubella and Mumps: BIAVAX

    Vaccines which are genetically engineered

    Hepatitis B: Merck

    Hepatitis B: SmithKline Beecham

    Lyme (Lymerix): SmithKline Beecham

    RSV, Synapis: (MedImmune)

    Vaccines with animal and cattle parts

    Chicken pox (Varivax): fetal bovine serum: Merck

    Diphtheria, Tetanus, acellular Pertussis, Acel-immune, beef heart infusion: Lederle

    Diphtheria (Infanrix), bovine extract: SmithKline Beecham

    Flu (Flushfield): chick embryos: Wyeth:

    Flu (Fluzone): chicken embryos: Connaught

    Measles (Attenuvax): hydrolyzed gelatin: Merck

    Measles, Mumps and Rubella (M-M-RII), hydrolyzed gelatin: Merck

    Mumps (MuMpsvax): hydrolyzed gelatin: Merck

    Polio (Ipol): calf serum, monkey kidney cells: Pasteur Merieux

    Polio, oral (Orimune): kidney cells, calf serum: Lederle

    Rubella (Meruvax): hydrolyzed gelatin: Merck

    Rubella and Mumps (Biavax): hydrolyzed gelatin: Merck

    Vaccines using cattle material – (blood, fetal calf serum, meat broth) carry a risk of mad cow disease. In the list below, the asterisk (*) means that the cattle parts which are in the product are (illegally) NOT LISTED on the vaccine package insert.

    Polio: DPT contains: DPT – Diphtheria and Tetanus Toxoids and Pertussis Vaccine Adsorbed SmithKline Beecham Pharmaceuticals. Produced using aluminum phosphate, formaldehyde, ammonium sulfate, washed sheep red blood cells, glycerol, sodium chloride, thimerosal medium: porcine (PIG) pancreatic hydrolysate of casein.

    Anthrax: *BioPort DPT

    Certiva, Anthrax: *BioPort DPT

    Certiva, diphtheria, pertussis, tetanus: North American/Baxter International

    DPT (Infanrix): diphtheria, pertussis, tetanus: GlaxoSmithKline Beecham

    Hep A (*Havrix): hepatitis A: GlaxoSmithKline Beecham

    Hib (*ActHIB): haemophilus influenzae Type B: Aventis Pasteur

    Hib (*OmniHIB): haemophilus influenzae Type B: GlaxoSmithKline Beecham

    Pneumonia (*PNU-IMUNE 23): Lederle/American Home Products

    Polio (IPOL): Aventis Pasteur

    OUTSTANDING ONLINE SOURCES
    Here are several excellent sources for additional information. Flip back and forth through the various pages on each one, and you will discover a lot.

    Concerned Parents for Vaccine Safety Home Page sprynet.com

    Global Vaccine Awareness League gval.com

    Informed Parents Vaccination Home Page unc.ed

    Massachusetts Citizens for Vaccination Choice vaccinechoice.org

    National Vaccine Information Center 909shot.com

    Natural Immunity Information Network members/xoom.com

    New Atlantean Immunization Resources newatlantean.com

    PROVE (Parents Requesting Open Vaccine Education) swbell.net

    Stealth Virus Web Site ccid.org

    The Kidz Are People Too Page geocities.com

    Thinktwice Global Vaccine Institute thinktwice.com

    Vaccine Articles healthy.net

    Vaccination Awareness Network ozemail.com

    Vaccine Information and Awareness access1.net

    Vaccines: The Truth Revealed odomnet.com

    BOOKS ON CHILDHOOD VACCINATION
    If you want to do more research on the vaccine issue, here are 22 books to select from. They will prove invaluable.

    Buttram, Harold E., M.D., Vaccination and Immune Malfunction [He shows the many correlations between vaccinations and immunological disorders; also how to legally avoid immunizations.]

    Chaitow, Leon, Vaccination and Immunisation: Dangers, Delusions, and Alternatives [History of vaccines, long-term effects, and linkage to AIDS]

    Coulter, Harris L. Coulter, and Barbara Loe Fisher, A Shot in the Dark: Why the P in the DPT Vaccination May Be Hazardous to Your Child’s Health [About the DPT vaccine]

    Coulter, Harris L., Vaccination, Social Violence and Criminality [Connection between childhood shots and autism, hyperactivity, and learning disabilities]

    Cournoyer, Cynthia, What About Immunisations? Exposing the Vaccine Philosophy

    DeLatte, Yves, Vaccinations: The Untold Truth

    Elben, Peter, Vaccination Condemned

    Gunn, Trevor, Mass Vaccination: A Point in Question

    Horowitz, Leonard G., Emerging Viruses: AIDS and EBOLA: Nature, Accident or Intentional

    James, Walene, Immunisation – The Reality Behind the Myth

    Kalokerinos, A., M.D., Every Second Child [Correlates vaccinations, malnutrition, and reactions]

    Mendelsohn, Robert S., M.D., Immunizations: The Terrible Risks Your Children Face That Your Doctor Won’t Reveal [Author is an experienced pediatrician.]

    Mendelsohn, Robert S., M.D., How to Raise a Healthy Child in Spite of Your Doctor [Outstanding book]

    Miller, Neil Z., Vaccines: Are They Really Safe and Effective? A Parent’s Guide to Childhood Shots [In all his books, Miller does quality work.]

    Miller, Neil Z., Immunization Theory vs. Reality: Expos� on Vaccinations

    Miller, Neil Z., Immunizations: The People Speak! Questions, Comments, and Concerns About Vaccinations

    Mothering Magazine, Vaccinations: The Rest of the Story [a collection of vaccine articles, which you can get by e-mail: mother@ni.net]

    Mullins, Eustace, Murder by Injection

    Murphy, Jamie, What Every Parent Should Know about Childhood Immunization [How vaccines are made, true cause of lower disease rates in the twentieth century, plus many other topics]

    Snead, Eva Lee, M.D., Some Call it AIDS, I Call it Murder!! [The long term effects of vaccines, which include chronic fatigue, cancer, leukemia, lymphoma, birth defects, immunosuppression, etc.]

    Scheibner, Viera, Ph.D., Vaccination: 100 Years of Orthodox Research Shows that Vaccines Represent a Medical Assault on the Immune System [Information connecting SIDS and DPT and other vaccines]

    Sinclair, Ian, Vaccination: The Hidden Facts

    MEDICAL JOURNAL ARTICLES
    Here are 188 authoritative medical research articles in professional journals, which verify in gory detail the dangers and ineffectiveness of vaccines. Think not that this ongoing tragedy is unknown to medical science. Hundreds of research reports have been made on the subject. The titles of the research reports have been placed in bold print. Just scan down through them and see for yourself! The proof is here!

    MMR VACCINE:

    “Optic Neuritis Complicating Measles, Mumps and Rubella Vaccination,” American Journal of Opthalmology 1978:86 [4 pp.]

    “Mumps Meningitis Following Measles, Mumps and Rubella Immunization,” Lancet July 1989 [1 p.]

    “Pancreatis Caused by Measles, Mumps, and Rubella Vaccine,” Pancreas Vol. 6 No. 4 1991 [2 p.]

    “A Prefecture-wide Survey of Mumps Meningitis Associated with Measles, Mumps and Rubella Vaccine,” Infec Dis J 1991 Vol. 10 pp. 204-209

    “Risk of Aseptic Meningitis after Measles Mumps and Rubella Vaccine in UK Children,” Lancet April 93 P.979

    “A Prefecture-Wide Survey of Mumps Meningitis Associated with Measles, Mumps, and Rubella Vaccine,” Pediatr Infect Dis J 1991;10 [6 pp.]

    “Guillain-Barr� syndrome after measles, mumps, and rubella vaccine,” Lancet Jan 1 1994 Vol. 343 [1 p.]

    “Bilateral Hearing Loss after Measles and Rubella Vaccination in an Adult,” New England Journal of Medicine, July 11 1991 p. 134 [1 p.] (9 cases of hearing loss after MMR vaccination)

    “Arthritis after Mumps and Measles Vaccination,” Arch Dis Child 1995;72 [2 pp.]

    RUBELLA VACCINE: [also see MMR]

    “Rubella Vaccination of Hospital Employees,” JAMA Feb. 20, 1981 Vol. 245 No 7 [2 pp.] (Physicians rarely take the vaccines themselves!)

    “Two Syndromes Following Rubella Immunization,” AMA 1970 Vol. 214 No. 13 [5 pp.]

    “Chronic Arthritis after Rubella Vaccination,” Clinical Infec Dis. 1992 15;307-12 [6 pp.]

    “Acute Arthritis Complicating Rubella Vaccination,” Arthritis and Rheumatism 1971 41 [4 pp.]

    “Joint Symptoms Following an Area Wide Rubella Immunization Campaign Report of a Survey,” Am J of Public Health Vol. 62 No. 5 [4 pp.]

    “Polyneuropathy Following Rubella Immunization,” Am J Dis Child 1974 Vol. 127 [5 pp.]

    “Postpartum Rubella Immunization: Association with Development of Prolonged Arthritis, Neurological Sequelae, and Chronic Rubella Viremia,” Journal of Infectious Diseases 1985 Vol. 152 No. 3 [7 pp.]

    “Serological Evidence of Reinfection among Vaccinees during Rubella Outbreak,” Lancet Vol. 336 p. 1071 [1 p.]

    “Diffuse Myelitis Associated with Rubella Vaccination,” BMJ Oct. 1976 [2 pp.]

    MEASLES VACCINE: [also see MMR]

    “Neurological disorders Following Live Measles-Virus Vaccination.” JAMA March 1973, Vol. 223 No. 13 [4 pp.] (A research study of measles vaccines causing neurologic damage over a 12-year period [1961-1973] estimated that one child in every thousand receiving the vaccine will develop severe neurologic damage)

    “Guillain-Barr� Syndrome Following Administration of Live Measles Vaccine.” Amer J of Med 1976 Vol. 60 [3 pp.]

    “Thrombocytopenic Purpura Following Vaccination with Attenuated Measles Virus,” Amer J Dis Child Jan. 1968 Vol. 115 [3 pp.]

    “Investigation of a measles outbreak in a fully vaccinated school population including serum studies before and after revaccination,” Pediatr Infec Dis J 1993 12 [8 pp.]

    “Risk of Aseptic Meningitis after Measles, Mumps, and Rubella Vaccine in UK Children,” Lancet 1993 Vol. 341 [4 pp.]

    “Failure of Measles Vaccine Sprayed into the Oropharynx of Infants,” Lancet May 1983 [1 p.] (This is on an inhaled vaccine, using the E-Z strain, not a shot vaccine.)

    “High Titre Measles Vaccine Dropped,” Lancet 1992 Vol. 340 [1 p.] (Using the Experimental E-Z Measles vaccine)

    “Failure to Reach the Goal of Measles Elimination,” Arch Intern Med 1994 Vol. 154 [6 pp.]

    “A Measles Outbreak at a College with Rematriculation Immunization Requirements,” Am J of Pub Health Vol. 81 No. 3 [4 pp.]

    “An explosive point-source measles outbreak in a highly vaccinated population,” American Journal of Epidemiology 1989 Vol. 129 No. 1 [p. 10]

    “Atypical measles in children previously immunized with attenuated measles virus vaccines,” Pediatrics, Vol. 50 No. 5 [6 pp.]

    “A Persistent Outbreak of Measles Despite Appropriate Prevention and Control Measures,” American Journal of Epidemiology Vol. 126 No. 3 [13 pp.]

    “Exaggerated Natural Measles Following Attenuated Virus Immunization,” Pediatrics, 1976 Vol. 57 No. 1 [3 pp.]

    “Child Mortality After High-Titre Measles Vaccines.” Lancet Vol. 338 1991 [4 pp.]

    “Thrombocytopenia after Immunization with Measles Vaccines, Review of the Vaccine Adverse Events Reporting System (1990 to 1994),” Ped Infect Dis J Vol. 15 No. 1 Jan. 1996 [3 pp.]

    “Measles, Vaccine, and Crohn’s Disease,” Gastroenterology Vol. 108 No. 3 1995 [3 pp.]

    “Severe Hypersensitivity or Intolerance Reactions to Measles Vaccine in Six Children,” Allergy 1980 35 [7 pp.]

    “Pathogenesis of Encephalitis Occurring with Vaccination , Variola, and Measles,” Arch of Neurology and Psychiatry 1938 Vol. 39 [8 pp.]

    “Aseptic Meningitis after Vaccination Against Measles and Mumps.” Pediatr Infec Dis J 1989 8 pp. 302-308 [7 pp.]

    “Measles Vaccine Associated Encephalitis in Canada,” Lancet Sept. 1983 [2 pp.]

    “Pancreatitis Caused by Measles, Mumps, and Rubella Vaccine,” Pancreas Vol. 6 No. 4 [2 pp.]

    “Measles, Vaccine, and Neurological Events,” Lancet May 1997 [2 pp.]

    “Measles Vaccine Failures: Lack of Sustained Measles-Specific Immunoglobulin G Responses in Revaccinated Adolescents and Young Adults,” Pediatr Infect Dis J 1994; 13 [4 pp.]

    MUMPS VACCINE: [also see MMR]

    “Mumps Outbreak in a Highly Vaccinated School Population/evidence for large scale vaccination failure,” Arch Pediatr Adolesc Med 1995 Vol. 149 [5 pp.] (54 students developed mumps; 53 of them had been fully immunized against mumps.)

    “Aseptic Meningitis as a Complication of Mumps Vaccination,” Ped Infec Dis J 1991 Vol. 10 No. 3 [5 pp.]

    “A Large Outbreak of Mumps in the Postvaccine Era,” J of Infect Dis Vol. 158 No. 6 1988 [8 pp.]

    “Guillain-Barr� Syndrome occurrence following combined mumps-rubella vaccine,” Am J Dis Child Vol. 125 1973 [2 pp.]

    “Mumps, Vaccines, and Meningitis/ Heterogeneous Mumps Vaccine,” Lancet Vol. 340 1992 [2 pp.] (Urabe strain vaccine)

    “Mumps Vaccine and Nerve Deafness,” Amer J Dis Child Vol. 123 1972 [1 p.]

    Flu Vaccine: Neuropathy after Influenza Vaccination,” The Lancet Jan. 29, 1977 [2 pp.] (Swine flu vaccine)

    “Isolated Hypoglossal Nerve Paralysis Following Influenza Vaccination,” Am J Dis Child 1976 Vol. 130 [2 pp.]

    “Guillain-Barr� Syndrome,” Lancet Sept. 1978 [1 p.]

    “Relapsing Encephalomyelitis Following the use of Influenza Vaccine,” Arch Neurol Vol. 27 1972 [2 pp.]

    “Anaphylactoid allergic reactions to influenza and poliomyelitis vaccines,” Annals of Allergy Vol. 18 1960 [4 pp.]

    “A Neurological Note on Vaccination against Influenza,” British Med J Sept 1971 [2 pp.]

    “Optic Atrophy Following Swine Flu Vaccination,” Annals of Opthalmology July 1980 [3 pp.]

    “Meningoecephalitis Following an Influenza Vaccination,” Medical Intelligence Vol. 283 No. 22 [1 p.]

    POLIO VACCINE:
    “Shedding of Virulent Poliovirus Revertants during Immunization with Oral Poliovirus Vaccine after Prior Immunization with Inactivated Polio Vaccine,” J of Infect Dis 1993; 168 [5 pp.] (As many as 80% of the babies can infect those who touch their stools with polio)

    “Anaphylactoid allergic reactions to influenza and poliomylitis vaccines,” Annals of Allergy Vol. 18 1960 [4 pp.]

    “Vaccine Associated Poliomyelitis,” Lancet March 1994 Vol. 343 [3 pp.]

    “Vaccine Associated Paralytic Poliomyelitis,” New England J of Med 1993 [1 p.]

    “Cluster of Childhood Guillain-Barr� Cases after an Oral Poliovaccine Campaign,” Lancet Aug. 1989 [2 pp.]

    “Poliomyelitis and Prophylactic Inoculation against Diphtheria, Whooping Couch and Smallpox,” Lancet Dec 1956 pp. 6955 [9 pp.] (DPT and smallpox vaccines increase the likelihood of contracting polio.)

    “Residual Paralysis after Poliomyelitis Following Recent Inoculation,” Lancet June 1952 pp. 1187 [3 pp.] (Increase in polio after DPT shots)

    “Preparation of Poliovirus in a Human Fetal Diploid Cell Strain,” Am J Hyg 1962 Vol. 75 [10 pp.]

    “Outbreak of Paralytic Poliomyelitis in Finland; Widespread Circulation of Antigenically Altered Poliovirus Type 3 in a Vaccinated Population,” Lancet June 1986 [6 pp.] (A polio outbreak in a vaccinated population. Many who contracted polio had earlier received injections of IVP; some even had up to 5 doses of the vaccine.)

    “The Relation of Prophylactic Inoculations to the Onset of Poliomyelitis,” Lancet April 5, 1950 [5 pp.]

    “More on Vaccine Associated Paralytic Poliomyelitis,” New England Journal of Medicine Dec. 23, 1993 [2 pp.]

    “Intramuscular Injections within 30 Days of Immunization with Oral Poliovirus Vaccine. A Risk Factor for Vaccine associated with Paralytic Poliomyelitis,” New England Journal of Medicine Feb. 1995 [7 pp.]

    “Neurologic Complications in Oral Polio Vaccine Recipients,” J of Ped June 1986 [4 pp.]

    “Outbreak of Paralytic Poliomyelitis in Oman: Evidence for Widespread Transmission among Fully Vaccinated Children,” Lancet 1991 Vol. 338 [6 pp.]

    “Immune Response of Infants in Tropics to Injectable Polio Vaccine,” BMJ Jan. 1982 [1 p.] (About injected polio vaccine. This article mentions that oral polio vaccine in a series of 3 shots is only about 78% effective and vaccine failure is common.)

    “Vaccine Associated Paralytic Poliomyelitis,” New England J of Med Sept. 193 Vol. 329 [1 p.]

    SMALLPOX VACCINE:
    “Re-emergence of human monkeypox in Zaire in 1996,” Lancet May 1997 [1 p.]

    PERTUSSIS VACCINE: [also see DPT]
    “Hell’s Fire and Varicella Vaccine Safety,” New England j of Med 1988 Vol. 318 [3 pp.]

    DPT VACCINE:
    “Infectious Episodes Following Diphtheria Pertussis Tetanus Vaccination,” Clinical Pediatrics Oct. 1988 [8 pp.] (Regardless of the age at which the children received the DPT vaccine, a sizeable percentage of them experienced sickness and/or physical damage.)

    “Encephalopathy Following Diphtheria Pertussis Inoculation,” Arch Dis Childhood Vol. 28 1953 [1 p.]

    “Fatal Anaphylactic Shock occurrence in identical twins following second injection of diphtheria toxoid and pertussis antigen,” JAMA June 1946 [6 pp.]

    “Pertussis Vaccination and Asthma: is there a link?” JAMA 1994 Vol. 272 No. 8 [1 p.]

    “Further Contributions to the Pertussis Vaccine Debate,” Lancet May 16 1981 pp. 1113 [2 pp.]

    “The Whooping Cough Immunization Controversy,” Arch Dis Child 1981 Vol. 56 [4 pp.]

    “Workshop on Neurologic Complications of Pertussis and Pertussis Vaccination,” Neuropediatrics 1990 Vol. 21 [6 pp.] (This article mentions that, in evaluating side-reactions to the vaccine, researchers should keep four facts in mind: [1] Vaccines are not standardized between manufacturers. [2] For a given manufacturer, vaccines are not standard from one batch to the next. [3] Unless the vaccine is properly prepared and refrigerated, its potency and reactivity varies with shelf life. [4] The entire question of vaccine detoxification has never been systematically investigated.)

    “Encephalopathy Following Pertussis Vaccine Prophylaxis,” JAMA Vol. 141 [3 pp.]

    “Encephalopathy Following Diphtheria Pertussis Inoculation,” Arch of Dis Child Vol. 28 1953 [2 pp.]

    “Mortality and Morbidity from Invasive Bacterial Infections during a Clinical Trial of acellular Pertussis Vaccines in Sweden,” Pediatri Infect Dis J 1988 7 [8 pp.]

    “Adverse reactions after injection of absorbed diphtheria-pertussis-tetanus (DPT) vaccine are not due only to pertussis organisms or pertussis components in the vaccine,” Vaccine Vol. 9 1991 [4 pp.]

    “Pertussis Encephalopathy with a Normal Brain Biopsy and Elevated Lymphocytosis Promoting Factor Antibodies,” Pediatric Infectious Disease 1984 Vol. 3 No. 5 [4 pp.] (A vaccinated child against whooping cough, in addition to developing encephalopathy)

    “Neurological Complications of Pertussis Inoculation,” Arch Dis in Childhood 1974; 49 [4 pp.]

    “Encephalopathies Following Prophylactic Pertussis Vaccine,” Pediatrics Vol. 1 1948 [20 pp.]

    “Bordetella Parapertussis,” Am J Dis Child 1977 Vol. 131 [4 pp.] A discussion about another type of pertussis, which the vaccine does not cover, but which has the same symptoms of whooping cough. The article explains how, during pertussis outbreaks, many cases were actually parapertussis instead.)

    “Pertussis Vaccine Encephalopathy,” JAMA 1990 Vol. 264 [4 pp.]

    “Recurrent Seizures after Diphtheria, Tetanus, and Pertussis Vaccine Immunization,” AJDC Oct. 1984 Vol. 138 [3 pp.]

    “DTP-Associated Reactions: An Analysis by injection Site, Manufacturer, Prior Reactions, and Dose,” Pediatrics Vol. 73 No. 1 [3 pp.]

    “Nature and Rates of Adverse Reactions Associated with DTP and DT Immunizations in Infants and Children,” Pediatrics Vol. 68 No. 5 [10 pp.]

    “Anaphylaxis Due to Vaccination in the Office,” Can Med Assoc J Vol. 134 Feb. 1986 [2 pp.]

    “Encephalopathy after Combined Diphtheria Pertussis Inoculation,” Lancet 1950 [3 pp.]

    “Increased Intercranial Pressure after Diphtheria, Tetanus, and Pertussis Immunization,” American J of Disease of Childhood Vol. 133 Feb. 1979 [2 pp.]

    “Reactions to Pertussis Vaccine,” Lancet May 28 1983 [2 pp.]

    “Reactions to Combined Vaccines Containing Killed Bordetella Pertussis,” The Medical Officer Feb. 1967 [4 pp.]

    “Abscesses Complicating DTP Vaccination,” Am J Dis Child Vol. 135 Sept 1981 [3 pp.]

    “Acellular and Whole Cell Pertussis Vaccines in Japan,” JAMA Vol. 257 No. 10 1987 [6 pp.]

    “Infectious Episodes Following Diphtheria Pertussis Tetanus Vaccination,” Clinical Pediatrics Oct. 1988 [4 pp.] (At whatever age the child received the DPT vaccine, a sizeable percentage experienced varying levels of sickness and/or physical damage).

    “Seizures Following Childhood Immunizations,” J of Pediatrics Vol. 102 No. 1 [7 pp.]

    “Bulging Anterior Fontanel after DPT Vaccination,” The Indian J of Ped 1994 Vol.. 61 No. 1 [2 pp.]

    “Illness after Whooping Cough Vaccination,” The Medical Officer Oct. 1961 pp. 241 [4 pp.] (I think this is an excellent article to have on hand.)

    “Encephalopathy Following Pertussis Vaccine Prophylaxis,” JAMA Vol. 141 No. 8 [3 pp.]

    “Vaccination Against Whooping-Cough,” Lancet Jan. 1977 [4 pp.]

    “Rectal Temperature of Normal Babies the Night after First Diphtheria, Pertussis, and Tetanus Immunization,” Arch Dis in Childhood 1990; 65 [3 pp.]

    “Is Universal Vaccination against Pertussis Always Justified?” BMJ Oct. 22, 1960 [3 pp.]

    “Complication of Pertussis Immunization,” BMJ Aug. 30, 1958 [1 p.]

    “Reactions after Pertussis Vaccine: A Manufacturer’s Experiences and Difficulties Since 1964,” BMJ April 1978 [7 pp.]

    “Idiosyncrasy to Whooping-Cough Vaccine,” BMJ Dec. 1949 [1 p.]

    “Frequent Symptoms after DTPP Vaccinations” (Arch Dis in Child 1991 Vol. 66 [5 pp.]

    “Rectal Temperature of Normal Babies the Night after Diphtheria, Pertussis, and Tetanus Immunization,” Arch Dis in Childhood 1990; 65 [3 pp.]

    “The 1993 Epidemic of Pertussis in Cincinnati Resurgence of Disease in a Highly Immunized Population of Children,” New England J of Med July 7, 1994 [6 pp.]

    “Neurological Complications of Pertussis Immunization,” BMJ July 5, 1958 [3 pp.]

    “History of Convulsions and Use of Pertussis Vaccine,” Jof Peds Aug. 1985 [5 pp.]

    “Pertussis Immunisation and Serious Acute Neurological Illness in Children,” BMJ Vol. 282; 1981 [5 pp.]

    “Toxic and Reactogenic Properties of Pertussis Bacteria,” Journal of Hygiene, Epidemiology, Microbiology, and Immunology 1975 No. 3 [12 pp.]

    “Relationship of Pertussis Immunization to the Onset of Neurological Disorders: A Retrospective Epidemiologic Study,” J Pediatr 1988; 113 [5 pp.]

    “Further Experience of Reactions, Especially of a Cerebral Nature in conjunction with Triple Vaccination: A Study Based on Vaccinations in Sweden 1959-1965,” BMJ 1967 [4 pp.]

    TETANUS VACCINE: [also see DPT]
    “Acute Transverse Mylelitis after Tetanus Toxoid Vaccination,” Lancet May 1992 Vol. 339 [2 pp.]

    “Adverse Reactions to Tetanus Toxoid,” JAMA may 1994 Vol. 271 [1 p.]

    “Unusual Neurological Complications Following Tetanus Toxoid Administration,” J Neurology 1977; 215 [2 pp.]

    “Guillain-Barr� Syndrome after Combined Tetanus-Diphtheria Toxoid Vaccination,” J Neurological Sciences 1997 147 [2 pp.]

    “Abnormal T-Lymphocyte Subpopulations in Healthy Subjects After Tetanus Booster Immunization,” New England Journal of Medicine Jan. 1984 [2 pp.]

    “Relapsing Neuropathy Due to Tetanus Toxoid,” Journal of the Neurological Sciences 1978; 37 [13 pp.]

    DIPHTHERIA VACCINE: [also see DPT]
    “Molecular Epidemiology of the 1984-1986 Outbreak of Diphtheria in Sweden,” New England J of Med Jan 1988 Vol. 318 [3 pp.]

    HEP B VACCINE (Hepatitis B Vaccine):
    “Acute Hepatitis B Infection after Vaccination,” Lancet Vol. 345 Jan. 1995

    “Multiple Evanescent White Dot Syndrome after Hepatitis B Vaccine,” American J of Ophthalmology Vol. 122 No. 3 [2 pp.]

    “Systemic Lupus Erythematosus and Vaccination against Hepatitis B,” Nephron 1992; 62 [1 p.]

    “Hepatitis B Vaccines: Reported Reactions,” WHO Drug Info Vol. 4 1990 [1 p.]

    “Postmarketing Surveillance for Neurologic Adverse Events Reported after Hepatitis B Vaccination,” American J of Epidemiology Vol. 127 No. 2 [16 pp.]

    “Severe Acute Hepatitis B Infection after Vaccination,” Liver Dysfunction and DNA Antibodies after Hepatitis B Vaccination

    “Thrombocytopenic Purpura after Recombinant Hepatitis B Vaccine,” Lancet Vol. 344 [2 pp.]

    “Central Nervous System Demyelination after Immunization with Recombinant Hepatitis B Vaccine,” lancet Vol. 338 1991 [2 pp.]

    “Pulmonary and Cutaneous Vasculitis Following Hepatitis B Vaccination,” Thorax 1993 Vol. 48 [2 pp.]

    “Reactions to Thimerosal in Hepatitis B Vaccines,” Dermatologic Clinics Vol. 8 No. 1 Jan. 1990 [4 pp.]

    “Acute Posterior Multifocal Placoid Pigment Epitheliopathy after Hepatitis B Vaccine,” Arch Ophthalmology Vol. 113 March 1995 [4 pp.]

    “Gullian-Barr� Syndrome Following Immunization with Synthetic Hepatitis B Vaccine,” New Zealand Med J March 1989 [2 pp.]

    “Hypersensitivity to Thiomersal in Hepatitis B Vaccine,” Lancet Vol. 338 1991 [1 p.]

    “Polyneuropathy Associated with Administration of Hepatitis B Vaccine,” New England J of Med Sept. 1983 [1 p.]

    “Evans’ Syndrome Triggered by Recombinant Hepatitis B Vaccine,” Clinical Infect Dis 1992; 15 [1 p.]

    “Polyneuropathy Associated with Administration of Hepatitis B Vaccine,” New England J of Med Sept 1983 [1 p.]

    HIB VACCINE (Haemophilus Influenzae):

    Note: HIB is a type of meningitis; it is not variant form of influenza.

    “Acute Inflammatory Demyelinating Polyradiculoneuropathy (Guillain-Barr� Syndrome) after Immunization with Haemophilus Influenzae Type b Conjugate Vaccine,” Journal of Pediatrics 1986 Vol. 115 [4 pp.]

    “Lack of Efficacy of Haemophilus b Polysaccharide Vaccine in Minnesota,” JAMA 1988 Vol. 260 No. 10 [6 pp.]

    “b-CAPSA I Haemophilus Influenzae, Type b, Capsular Polysaccharide Vaccine Safety,” Pediatrics Vol. 79 No. 3 1987 [5 pp.]

    MENINGOCOCCAL VACCINE:

    “Adverse Events Temporally Associated with Meningococcal Vaccines,” Can Med Ass J Feb. 1996 Vol. 154 [3 pp.]

    PNEUMOCOCCAL VACCINE:

    “A Reassessment of Pneumococcal Vaccine,” New England J of Med 1984 Vol. 310 No. 10 [3 pp.]

    AIDS VACCINE:

    “AIDS Vaccine Conference,” Science Vol. 266 Nov. 94 [1 p.]

    MISCELLANEOUS ON VACCINES:

    “Myocardial Complications of Immunizations,” Annals of Clinical Research 1978 Vol. 10 [8 pp.]

    “Adverse Events Associated with Childhood Vaccines Other Than Pertussis and Rubella,” JAMA Vol. 271 No. 20 [4 pp.]

    “Seizures following Childhood Immunizations,” Journal of Ped Vol. 102 No. 1 [5 pp.]

    “Vaccine Damage,” Lancet Jan. 1997 [1 p.]

    “Sudden Death amoung Finnish Conscripts,” British Med J 1976 [3 pp.] (About vaccines which cause death due to damage to heart)

    “Childhood Immunization and Diabetes Mellitus,” New Zealand Medical Journal May 1996 [1 p.]

    “Allergic Reaction Associated with Viral Vaccines,” Progr Med Virol Vol. 13 pp. 239-270 [17 pp.]

    “Immunization Practices of Primary Care Practitioners and Their Relationship to Immunization Levels,” Arch Pediatr Adolesc med/Vol 148 Feb. 1994 [9 pp.]

    “Regression of Hodgkin’s Disease after Measles,” Lancet May 1981 [1 p.]

    “Depression of Tuberculin Sensitivity Following Measles Vaccination,” American Review of Respiratory Diseases 1964 Vol. 90 [5 pp.]

    “Incentive for Measles Mumps, and Rubella Vaccination,” Lancet March 1989 p. 496 [1 p.] (Suggests a pilot program which will pay parents to get them to bring children for immunization)

    “Frequent Symptoms after DTPP Vaccination,” Arch Dis in Child 0ct.-Dec. 1991 Vol. 66 [5 pp.] (DPT combined with Polio vaccine)

    “Risk of Virus Transmission by Jet Injection,” Lancet Jan. 1988 [1 p.] (Dangers of using jet injectors to vaccinate)

    “Dermatomyositis and Vaccination,” Lancet May 1978 [2 pp.]

    “Litigation Causes Huge Price Increases in Childhood Vaccines,” Lancet June 1986 pp. 1339 [1 p.]

    “Allergic Reactions to Tetanus, Diptheria, Influenza and Poliomyelitis Immunizations,” Annals of Allergy Vol. 20 1962 [5 pp.]

    “Malignant Tumors as a Late Complication of Vaccination,” Arch Derm Vol. 98 1968 [4 pp.]

    “Vaccine-Induced Autoimmunity,” Journal of Autoimmunity 1996 Vol. 9 [5 pp.]

    “Depressed Lymphocyte Function after MMR Vaccination,” Journal of Infec Dis.Vol. 132 No. 1 1975 [4 pp.]

    “Vaccines and Antiviral Drugs,” Epidemiology of Viral Infect. Vol. 86 (Has a small paragraph on the use of human aborted fetal tissue)

    “Complications of Immunization,” Ped in Review Vol. 18 No. 2 1997 [2 pp.] (lists some risk factors)

    “Repeated Immunizations: Possible Adverse Effects,” Annals of Intern. Med 1974 81; 594-600 [6 pp.]

    “Neurological Complications of Immunization,” Annals of Neurology Aug. 1982 [10 pp.]

    “Multiple Sclerosis and Vaccination,” BMJ April 1967 [4 pp.]

    “Increase in Asthma Correlates with Less Childhood Infection,” Lancet Jan.1997 [1 p.]

    “Multiple Sclerosis and Vaccination,” BMJ April 1967 [4 pp.]

    “lleal-lymphoid-nodular Hyperplasia, Non-specific Colitis and Pervasive Developmental Disorder in Children,” Lancet Vol. 351 Feb. 1998 [5 pp.]

    “Vaccines,” BMJ July 1967 [1 p.]

    “Inoculation and Poliomyelitis,” BMJ July 1950 [6 pp.]

    “Vitamin A Supplements: Too Good Not To Be True,” New England J of Med 323 No. 14 [2 pp.] (The use of vitamin A to help fight natural measles infection)

    THE SIDS-VACCINE CONNECTION:

    “Possible Temporal Association Between Diphtheria-Tetanus-Toxoid-Pertussis Vaccination and Sudden Infant Death Syndrome,” Pediatric Infectious Disease 1983 Vol. 2 No. 1 [5 pp.]

    “DTP Vaccination and Sudden Infant Deaths—Tennessee,” MMWR March 23,1979 [2 pp.]

    “Characteristics of Diphtheria-Pertussis- Tetanus (DPT) Post-vaccinal Deaths and DPT-Caused Sudden Infant Death Syndrome (SIDS): A Review,” Neurology April 1986 [2 pp.]

    ABORTED FETAL TISSUE IN VACCINES:
    The following research studies are about vaccines which use tissue (flesh or organs) taken from aborted human babies.

    “Studies of Immunization with Living Rubella Virus,” Amer J Dis Child Vol. 110 Oct. 1965 [7 pp.] (More on aborted fetal tissue. The article states: “This fetus was from a 25 year old mother exposed to rubella 8 days after last menstrual period. 16 days later she developed rubella. The fetus was surgically aborted 17 days after maternal illness and dissected immediately. Explants from several organs were cultured and successful cell growth was achieved from lung, skin, and kidney. It was then grown on WI-38. This new vaccine was tested on orphans in Philadelphia.” Special note by present author: An “explant” is “living tissue transferred from an organ to an artificial medium for culture” [Stedman’s Medical Dictionary, p. 550]. Therefore the baby was still alive when part of its tissue was placed in the culture, where those cells continued to live. The next citation, immediately below, reveals that the explants are cut off while the baby is still living.)

    “Attenuation of RA 27/3 Rubella virus in WI-38 Human Diploid Cells,” Amer J Dis Child Vol. 118 1969 [7 pp.] (More on use of aborted fetal tissue. The report states: “Explant cultures were made of the dissected organs of a fetus aborted because of rubella, the 27th in our series of fetuses aborted during the 1964 epidemic.”)

    “Gamma Globulin Prophylaxis; Inactivated Rubella Virus; Production and Biologics Control of Live Attenuated Rubella Virus Vaccines,” Amer J Dis Child 1969 Vol. 118 [10 pp.] (This contains information on the use of human aborted fetal tissue cells in rubella vaccine. Mentions the danger of human genetic material passing over into the vaccine.)

    “Economical Multiple-site Intradermal Immunization with Human Diploid-Cell-Strain Vaccine Is Effective for Post Rabies Prophylaxis,” Lancet May 1985 [4 pp.]

    “The Serial Cultivation of Human Diploid Cell Strains,” Experimental Cell Research Vol. 26 1961 [19 pp.]

    “Production and Testing of Rubella Virus Vaccine,” Amer J Dis Child 1969 Vol. 118 pp. 367 [5 pp.] (More on the use of aborted fetal tissue cells)

    “The in vitro growth of rubella virus in human embryo cells,” Am J of Epidemiology Vol. 81 No. 1 [7 pp.] (More on aborted fetal tissue)

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    VACCINATION INSIGHTS AND DATA

     

     

    When things just don’t add up!

    Alarming language by the Center for Disease Control (CDC) and World Health Organization (WHO)

    have hinted of mandatory Swine (H1N1) Flu Vaccinations in the near future!

    Webster’s Dictionary defines a “Pandemic” as occurring over a wide geographical area and affecting an

    exceptionally high proportion of the population. (emphasis in bold added)

    STATISTICS as of 8/7/09:

    Worldwide: U.S.A. Percentage in U.S.A.

    Population: 6,706,993,152 304,059,724 N/A

    Annual Deaths from Regular Flu: 250,000 – 500,000 36,000 .000118%

    Reported Swine Flu Cases: 149,781 43,771 .000143%

    Reported Swine Flu Deaths: 1,030 477 .000001568%

    Would you consider this a pandemic?

    Interestingly, as of July 24th, Dr. Anne Schuchat, Dir. of

    CDC’s National Center, stated, “Friday morning’s posting of

    confirmed cases will be the last such posting because the CDC wants

    to de-emphasize testing for the virus.” * (The Arizona Republic, 7/25/09, Pg.7)

    *If a “pandemic” truly exists, and considering the gravity of being mandated (forced) to

    have untested, dangerous, toxic chemicals (see reverse side) injected into our bodies or

    our children’s, wouldn’t monitoring specific symptoms and cases of Swine Flu be critical?

    Think about the numerous side effects following each TV drug

    commercial and this untested Swine (H1N1) Flu Vaccine!

     

    It’s your decision, but before you offer your arm or that of your child’s, know ALL the facts

    Drug manufacturers providing Swine (H1N1) Flu vaccines refuse to release entire mix of ingredients proclaiming proprietary rights, however, a few of just some of the known adjuvants and their side effects are:
    Aluminium: A heavy metal which can interfere with normal brain function.

    It’s a potent neurotoxin which can cause more neurologic disorders than Alzheimer’s disease.  “It is not just it’s connection with Alzheimer’s that makes aluminum such a danger to human physiology, it’s that aluminum can interfere with the formation and development of virtually a human nerve tissue in a fully unpredictable fashion.*

     

    Formaldehyde:  A carcinogenic embalming fluid and known to cause cancer. Vaccines are not tested for carcinogenicity.*

     

    Mercury:  A form of Thimerosal which is 49.5% mercury.  It is “ethylmercury,” a true neurotoxin (nerve killer), and may cause permanent nerve damage and autoimmune disorders.  Linked to Autism.*

     

    African Green Monkey’s Kidneys: “Diseased” flesh of African Green Monkeys (U.S. Patent No. 5911998).  Research the method of producing a virus vaccine from cell line.  (http://www.patentstorm.us/patents/5)  (http://www.fivedoves.com/letters/aug2009/shanthini86-5.htm)

    Squalene:  An organic polymer, and an oil-based adjuvant to generate concentrated, unremitting immune responses over long periods of time.  Squalene has never been approved as a vaccine adjuvant. It is called, “Freund’s Complete Adjuvant” and can cause permanent organ damage and irreversible disease – specifically autoimmune diseases. Squalene is contributed to the “Gulf War Syndrome.”  Soldiers developed arthritis, fibromyalgia, lymphadenopathy, rashes, photosensitive rashes, malar rashes, chronic fatigue, chronic headaches, abnormal body hair loss, non-healing skin lesions, aphthous ulcers, dizziness, weakness, memory loss, seizures, mood changes, neuropsychiatric problems, anti-thyroid effects, anaemia, elevated ESR (erythrocyte sedimentation rate), systemic lupus erythematosus, multiple sclerosis, deadly Amyotrophic Lateral Sclerosis, Raynaud’s phenomenon with paroxysms of lack of blood in fingers and toes, Sjorgren’s syndrome with blurred vision, chronic diarrhea, night sweats and low-grade fever.”   Dr. Viera Scheibner, Ph D. Principal Research Scientist (http://www.whale.to/vaccine/adjuvants.html)  Excellent well-referenced information: http://www.Mercola.com and search, “Squalene:  The Swine Flu Vaccine’s Dirty Little Secret Exposed.”

    NOTE:  FDA is “fast-tracking” clinical tests which should take 26 weeks, but the mere one to three weeks gives little time from now until October to test the safety and efficacy of the flu vaccine.  In these clinical trials, Squalene has been curiously left out!   (http://clinicaltrials.gov/ct2/show/NCT00943488)

     

    Legal Liability Immunity Protection for vaccine manufacturers, WHO, CDC, Federal Government and its agents if the Swine (H1N10 Flu vaccine causes   serious physical injury or death. Public Readiness and Emergency Preparedness Act Questions and Answers passed 2006 :             http://www.hhs.gov/disasters/emergency/manmadedisasters/bioterorism/medication-vaccine-qa.html

     

    Health Insurance Policy Exclusions state “experimental” drugs (FDA has NOT approved Swine (H1N1) Flu Vaccine) are not covered.  Insurance           companies abandoned coverage for damage to life and property due to Acts of God, Nuclear War and Nuclear Power Plant Accidents and     Vaccinations!  (emphasis added)

     

    Research Scandals Associated with Baxter Pharmaceuticals and Novartis Pharmaceuticals, both continue to be contracted by WHO to produce a pandemic vaccine.  (http://www.newsmax.com/health/vaccine_swine_flu/2009/07/07/232717.html)

    #208
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    Keymaster

    Vaccination (ANIMAL)

     

    by Catherine O’Driscoll (posted with permission)

    A team at Purdue University School of Veterinary Medicine conducted several studies (1,2) to determine if vaccines can cause changes in the immune system of dogs that might lead to life-threatening immune-mediated diseases. They obviously conducted this research because concern already existed. It was sponsored by the Haywood Foundation which itself was looking for evidence that such changes in the human immune system might also be vaccine induced. It found the evidence. The vaccinated, but not the non-vaccinated, dogs in the Purdue studies developed autoantibodies to many of their own biochemicals, including fibronectin, laminin, DNA, albumin, cytochrome C, cardiolipin and collagen. This means that the vaccinated dogs –“but not the non-vaccinated dogs”–were attacking their Own fibronectin, which is involved in tissue repair, cell multiplication and growth, and differentiation between tissues and organs in a living organism. The vaccinated Purdue dogs also developed autoantibodies to laminin, which is involved in many cellular activities including the adhesion, spreading, differentiation, proliferation and movement of cells. Vaccines thus appear to be capable of removing the natural intelligence of cells. Autoantibodies to cardiolipin are frequently found in patients with the serious disease systemic lupus erythematosus and also in individuals with other autoimmune diseases. The presence of elevated anti-cardiolipin antibodies is significantly associated with clots within the heart or blood vessels, in poor blood clotting, haemorrhage, bleeding into the skin, foetal loss and neurological conditions. The Purdue studies also found that vaccinated dogs were developing autoantibodies to their own collagen. About one quarter of all the protein in the body is collagen. Collagen provides structure to our bodies, protecting and supporting the softer tissues and connecting them with the skeleton. It is no wonder that Canine Health Concern’s 1997 study of 4,000 dogs showed a high number of dogs developing mobility problems shortly after they were vaccinated (noted in my 1997 book, What Vets Don’t Tell You About Vaccines). Perhaps most worryingly, the Purdue studies found that the vaccinated dogs had developed autoantibodies to their own DNA. Did the alarm bells sound? Did the scientific community call a halt to the vaccination program? No. Instead, they stuck their fingers in the air, saying more research is needed to ascertain whether vaccines can cause genetic damage. Meanwhile, the study dogs were found good homes, but no long-term follow-up has been conducted. At around the same time, the American Veterinary Medical Association (AVMA) Vaccine-Associated Feline Sarcoma Task Force initiated several studies to find out why 160,000 cats each year in the USA develop terminal cancer at their vaccine injection sites.(3) The fact that cats can get vaccine-induced cancer has been acknowledged by veterinary bodies around the world, and even the
    British Government acknowledged it through its Working Group charged with the task of looking into canine and feline vaccines(4) following pressure from Canine Health Concern. What do you imagine was the advice of the AVMA Task Force, veterinary bodies and governments? “Carry on vaccinating until we find out why vaccines are killing cats, and which cats are most likely to die.” In America, in an attempt to mitigate the problem, they’re vaccinating cats in the tail or leg so they can amputate when cancer appears. Great advice if it’s not your cat amongst the hundreds of thousands on the “oops” list. But other species are okay -right? Wrong. In August 2003, the Journal of Veterinary Medicine carried an Italian study which showed that dogs also develop vaccine-induced cancers at their injection sites.(5) We already know that vaccine-site cancer is a possible sequel to human vaccines, too, since the Salk polio vaccine was said to carry a monkey retrovirus (from cultivating the vaccine on monkey organs) that produces inheritable cancer. The monkey retrovirus SV40 keeps turning up in human cancer sites. It is also widely acknowledged that vaccines can cause a fast-acting, usually fatal, disease called autoimmune haemolytic anaemia (AIHA). Without treatment, and frequently with treatment, individuals can die in agony within a matter of days. Merck, itself a multinational vaccine manufacturer, states in The Merck Manual of Diagnosis and Therapy that autoimmune haemolytic anaemia may be caused by modified live-virus vaccines, as do Tizard’s Veterinary Immunology (4th edition) and the Journal of Veterinary Internal Medicine.(6) The British Government’s Working Group, despite being staffed by vaccine-industry consultants who say they are independent, also acknowledged this fact. However, no one warns the pet owners before their animals are subjected to an unnecessary booster, and very few owners are told why after their pets die of AIHA.

    A Wide Range of Vaccine-induced Diseases

     

    We also found some worrying correlations between vaccine events and the onset of arthritis in our 1997 survey. Our concerns were compounded by research in the human field. The New England Journal of Medicine, for example, reported that it is possible to isolate the rubella virus from affected joints in children vaccinated against rubella. It also told of the isolation of viruses from the peripheral blood of women with prolonged arthritis following vaccination.(7) Then, in 2000, CHC’s findings were confirmed by research which showed that polyarthritis and other diseases like amyloidosis, which affects organs in dogs, were linked to the combined vaccine given to dogs.(8) There is a huge body of research, despite the paucity of funding from the vaccine industry, to confirm that vaccines can cause a wide range of brain and central nervous system damage. Merck itself states in its Manual that vaccines (i.e., its own products) can cause encephalitis: brain inflammation/damage. In some cases, encephalitis involves lesions in the brain and throughout the central nervous system. Merck states that “examples are the encephalitides following measles, chickenpox, rubella, smallpox vaccination, vaccinia, and many other less well defined viral infections”. When the dog owners who took part in the CHC survey reported that their dogs developed short attention spans, 73.1% of the dogs did so within three months of a vaccine event. The same percentage of dogs was diagnosed with epilepsy within three months of a shot (but usually within days). We also found that 72.5% of dogs that were considered by their owners to be nervous and of a worrying disposition, first exhibited these traits within the three-month postvaccination period. I would like to add for the sake of Oliver, my friend who suffered from paralysed rear legs and death shortly after a vaccine shot, that “paresis” is listed in Merck’s Manual as a symptom of encephalitis. This is defined as muscular weakness of a neural (brain) origin which involves partial or incomplete paralysis, resulting from lesions at any level of the descending pathway from the brain. Hind limb paralysis is one of the potential consequences. Encephalitis, incidentally, is a disease that can manifest across the scale from mild to severe and can also cause sudden death. Organ failure must also be suspected when it occurs shortly after a vaccine event. Dr Larry Glickman, who spearheaded the Purdue research into post-vaccination biochemical changes in dogs, wrote in a letter to Cavalier Spaniel breeder Bet Hargreaves: “Our ongoing studies of dogs show that following routine vaccination, there is a significant rise in the level of antibodies dogs produce against their own tissues. Some of these antibodies have been shown to target the thyroid gland, connective tissue such as that found in the valves of the heart, red blood cells, DNA, etc. I do believe that the heart conditions in Cavalier King Charles Spaniels could be the end result of repeated immunisations by vaccines containing tissue culture contaminants that cause a progressive immune response directed at connective tissue in the heart valves. The clinical manifestations would be more pronounced in dogs that have a genetic predisposition the findings should be generally applicable to all dogs regardless of their breed.” I must mention here that Dr Glickman believes that vaccines are a necessary evil, but that safer vaccines need to be developed. Meanwhile, please join the queue to place your dog, cat, horse and child on the Russian roulette wheel because a scientist says you should.

     

    Vaccines Stimulate an Inflammatory Response

     

    The word “allergy” is synonymous with “sensitivity” and “inflammation”. It should, by rights, also be synonymous with the word “vaccination”. This is what vaccines do: they sensitise (render allergic) an individual in the process of forcing them to develop antibodies to fight a disease threat. In other words, as is acknowledged and accepted, as part of the vaccine process the body will respond with inflammation. This may be apparently temporary or it may be longstanding. Holistic doctors and veterinarians have known this for at least 100 years. They talk about a wide range of inflammatory or “-itis” diseases which arise shortly after a vaccine event. Vaccines, in fact, plunge many individuals into an allergic state. Again, this is a disorder that ranges from mild all the way through to the suddenly fatal. Anaphylactic shock is the culmination: it’s where an individual has a massive allergic reaction to a vaccine and will die within minutes if adrenaline or its equivalent is not administered. There are some individuals who are genetically not well placed to withstand the vaccine challenge. These are the people (and animals are “people”, too) who have inherited faulty B and T cell function. B and T cells are components within the immune system which identify foreign invaders and destroy them, and hold the invader in memory so that they cannot cause future harm. However, where inflammatory responses are concerned, the immune system overreacts and causes unwanted effects such as allergies and other inflammatory conditions. Merck warns in its Manual that patients with, or from families with, B and/or T cell immunodeficiencies should not receive live-virus vaccines due to the risk of severe or fatal infection. Elsewhere, it lists features of B and T cell immunodeficiencies as food allergies, inhalant allergies, eczema, dermatitis, neurological deterioration and heart disease. To translate, people with these conditions can die if they receive live-virus vaccines. Their immune systems are simply not competent enough to guarantee a healthy reaction to the viral assault from modified live-virus vaccines. Modified live-virus (MLV) vaccines replicate in the patient until an immune response is provoked. If a defence isn’t stimulated, then the vaccine continues to replicate until it gives the patient the very disease it was intending to prevent. Alternatively, a deranged immune response will lead to inflammatory conditions such as arthritis, pancreatitis, colitis, encephalitis and any number of autoimmune diseases such as cancer and leukaemia, where the body attacks its own cells. A new theory, stumbled upon by Open University student Gary Smith, explains what holistic practitioners have been saying for a very long time. Here is what a few of the holistic vets have said in relation to their patients: Dr Jean Dodds: “Many veterinarians trace the present problems with allergic and immunologic diseases to the introduction of MLV vaccines…” (9) Christina Chambreau, DVM: “Routine vaccinations are probably the worst thing that we do for our animals. They cause all types of illnesses, but not directly to where we would relate them definitely to be caused by the vaccine.” (10) Martin Goldstein, DVM: “I think that vaccines…are leading killers of dogs and cats in America today.” Dr Charles E. Loops, DVM: “Homoeopathic veterinarians and other holistic practitioners have maintained for some time that vaccinations do more harm than they provide benefits.” (12) Mike Kohn, DVM: “In response to this violation, there have been increased autoimmune diseases (allergies being one component), epilepsy, neoplasia , as well as behavioural problems in small animals.” (13)

     

    A Theory on Inflammation

    Gary Smith explains what observant healthcare practitioners have been saying for a very long time, but perhaps they’ve not understood why their observations led them to say it. His theory, incidentally, is causing a huge stir within the inner scientific sanctum. Some believe that his theory could lead to a cure for many diseases including cancer. For me, it explains why the vaccine process is inherently questionable. Gary was learning about inflammation as part of his studies when he struck upon a theory so extraordinary that it could have implications for the treatment of almost every inflammatory disease –including Alzheimer’s, Parkinson’s, rheumatoid arthritis and even HIV and AIDS. Gary’s theory questions the received wisdom that when a person gets ill, the inflammation that occurs around the infected area helps it to heal. He claims that, in reality, inflammation prevents the body from recognising a foreign substance and therefore serves as a hiding place for invaders. The inflammation occurs when at-risk cells produce receptors called All (known as angiotensin II type I receptors). He says that while At1 has a balancing receptor, At2, which is supposed to switch off the inflammation, in most diseases this does not happen. “Cancer has been described as the wound that never heals,” he says. “All successful cancers are surrounded by inflammation. Commonly this is thought to be the body’s reaction to try to fight the cancer, but this is not the case. “The inflammation is not the body trying to fight the infection. It is actually the virus or bacteria deliberately causing inflammation in order to hide from the immune system [author’s emphasis].” (14) If Gary is right, then the inflammatory process so commonly stimulated by vaccines is not, as hitherto assumed, a necessarily acceptable sign. Instead, it could be a sign that the viral or bacterial component, or the adjuvant (which, containing foreign protein, is seen as an invader by the immune system), in the vaccine is winning by stealth. If Gary is correct in believing that the inflammatory response is not protective but a sign that invasion is taking place under cover of darkness, vaccines are certainly not the friends we thought they were. They are undercover assassins working on behalf of the enemy, and vets and medical doctors are unwittingly acting as collaborators. Worse, we animal guardians and parents are actually paying doctors and vets to unwittingly betray our loved ones. Potentially, vaccines are the stealth bomb of the medical world. They are used to catapult invaders inside the castle walls where they can wreak havoc, with none of us any the wiser. So rather than experiencing frank viral diseases such as the ‘flu, measles, mumps and rubella (and, in the case of dogs, parvovirus and distemper), we are allowing the viruses to win anyway -but with cancer, leukaemia and other inflammatory or autoimmune (self-attacking) diseases taking their place.

     

    The Final Insult

     

    All 27 veterinary schools in North America have changed their protocols for vaccinating dogs and cats along the following lines; (15) however, vets in practice are reluctant to listen to these changed protocols and official veterinary bodies in the UK and other countries are ignoring the following facts. Dogs’ and cats’ immune systems mature fully at six months. If modified live-virus vaccine is giver after six months of age, it produces immunity, which is good for the life of the pet. If another MLV vaccine is given a year later, the antibodies from the first vaccine neutralise the antigens of the second vaccine and there is little or no effect. The litre is no “boosted”, nor are more memory cells induced. Not only are annual boosters unnecessary, but they subject the pet to potential risks such as allergic reactions and immune-mediated haemolytic anaemia. In plain language, veterinary schools in America, plus the American Veterinary Medical Association, have looked at studies to show how long vaccines last and they have concluded and announced that annual vaccination is unnecessary.(16-19) Further, they have acknowledged that vaccines are not without harm. Dr Ron Schultz, head of pathobiology at Wisconsin University and a leading light in this field, has been saying this politely to his veterinary colleagues since the 1980s. I’ve been saying it for the past 12 years. But change is so long in coming and, in the meantime, hundreds of thousands of animals are dying every year -unnecessarily. The good news is that thousands of animal lovers (but not enough) have heard what we’ve been saying. Canine Health Concern members around the world use real food as Nature’s supreme disease preventative, eschewing processed pet food, and minimise the vaccine risk. Some of us, myself included, have chosen not to vaccinate our pets at all. Our reward is healthy and long-lived dogs. It has taken but one paragraph to tell you the good and simple news. The gratitude I feel each day, when I embrace my healthy dogs, stretches from the centre of the Earth to the Universe and beyond.

    About the Author:

     

    Catherine O’Driscoll runs Canine Health Concern which campaigns and also delivers an educational program, the Foundation in Canine Healthcare. She is author of Shock to the System (2005; see review this issue), the best-selling book What Vets Don’t Tell You About Vaccines (1997, 1998), and Who Killed the Darling Buds of May? (1997; reviewed in NEXUS 4/04). She lives in Scotland with her partner, Rob Ellis, and three Golden Retrievers, named Edward, Daniel and Gwinnie, and she lectures on canine health around the world. For more information, contact Catherine O’Driscoll at Canine Health Concern, PO Box 7533, Perth PH2 1AD, Scotland, UK, email catherine@carsegray.co.uk , website http://www.canine-health-concern.org.uk. Shock to the System is available in the UK from CHC, and worldwide from Dogwise at http://www.dogwise.com.

     

    Endnotes

     

    1. “Effects of Vaccination on the Endocrine and Immune Systems of Dogs, Phase II”, Purdue University, November 1,1999, at

    http://www.homestead.com/vonhapsburg/haywardstudyonvaccines.html.

    2. See http://www.vet.purdue.edu/epi/gdhstudy.htm.

    3. See http://www.avma.org/vafstf/default.asp.

    4. Veterinary Products Committee (VPC) Working Group on Feline and Canine Vaccination, DEFRA, May 2001.

    5. JVM Series A 50(6):286-291, August 2003.

    6. Duval, D. and Giger,U. (1996). “Vaccine-Associated Immune-Mediated Hemolytic Anemia in

    the Dog”, Journal of Veterinary Internal Medicine 10:290-295.

    7. New England Journal of Medicine, vol.313,1985.

    See also Clin Exp Rheumatol 20(6):767-71, Nov-Dec 2002.

    8. Am Coll Vet Intern Med 14:381,2000.

    9. Dodds, Jean W.,DVM, “Immune System and Disease Resistance”, at

    http://www.critterchat.net/immune.htm.

    10. Wolf Clan magazine, April/May 1995.

    11. Goldstein, Martin, The Nature of Animal Healing, Borzoi/Alfred A. Knopf, Inc., 1999.

    12. Wolf Clan magazine, op. cit.

    13. ibid.

    14. Journal of Inflammation 1:3,2004, at http://www.journal-inflammation.com content/1/1/3.

    15. Klingborg, D.J., Hustead, D.R. and Curry-Galvin, E. et al., “AVMA Council on Biologic and Therapeutic Agents’ report on cat and dog vaccines”, Journal of the American Veterinary Medical Association 221(10):1401-1407, November 15,2002,

    http://www.avma.org/policies/vaccination.htm.

    16. ibid.

    17. Schultz, R.D., “Current and future canine and feline vaccination programs”, Vet Med 93:233254,1998.

    18. Schultz, R.D., Ford, R.B., Olsen, J. and Scott, P., “Titer testing and vaccination: a new look at traditional practices”, Vet Med 97:1-13, 2002 (insert).

    19. Twark, L. and Dodds, W.J., “Clinical application of serum parvovirus and distemper virus antibody liters for determining revaccination strategies in healthy dogs”, J Am Vet Med Assoc 217:1021-1024,2000.

     

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