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To Vaccinate or Not To Vaccinate?
Are Vaccines Safe or Effective?
We are faced with so much information nowadays that it is difficult to choose wisely for our children and ourselves as to what is always in our best interest. To vaccinate or not to vaccinate? Maybe some are effective while others have less of a track record of effectiveness? Some vaccines present safety issues right from the start. Then the question of whether or not we should be giving the sheer number of vaccines at such an early age that we are giving comes into question?
In order to be fair this page will have documentation that has both data that supports and is against vaccines of a variety of kinds. At this point in time we cannot advise the use of vaccinations due to the suggestive evidence that is currently on public record. What we have here is a lot of unanswered questions and safety concerns regarding all of the vaccines. This is to call into question both the safety and effectiveness of these instruments of modern health care.
If the concerns outweigh the benefits than we ought to rethink our position.
In order to be fair this page will have documentation that has both data that supports and is against vaccines of a variety of kinds. At this point in time we cannot advise the use of vaccinations due to the suggestive evidence that is currently on public record. What we have here is a lot of unanswered questions and safety concerns regarding all of the vaccines. This is to call into question both the safety and effectiveness of these instruments of modern health care.
If the concerns outweigh the benefits than we ought to rethink our position.
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DISCLAIMER: This page will be updated regularly as we are always researching. If you have research you wish us to put here fill-in the form on the left. Even though we primarily have data concerning the side effects of these vaccines it does not mean we oppose data that supports vaccines. We want to inform parents and the public at large of questions and observations that are of a significant concern regarding vaccination protocols, ingredients and reasons for use. We must review the data.
“The right thing to do never requires any subterfuge, it is always simple and direct.” Calvin Coolidge |
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What comes of a society that accepts foreign 'proven toxic' substances to be injected into their youth?
A profoundly irresponsible social experiment that degrades the immunity of our future!
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What comes of a society that accepts foreign 'proven toxic' substances to be injected into their youth?
A profoundly irresponsible social experiment that degrades the immunity of our future!
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A detailed study showing when vaccines were introduced and the decline of infectious disease. Did the vaccines cause the decline? Research this study and see for yourself. Thanks to Dr. Sherri Tenpenny for the PDF's and extensive research!
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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.
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The in vitro research in this new article examined: (1) the comparative toxicity of commonly used preservatives in US-licensed vaccines to human neurons; and (2) the compounds’ relative toxicity indices of these compounds derived by comparing their toxicity to human neurons to their toxicity to bacterial cells.
Using human neuroblastoma cells, this study showed that the relative toxicities of the compounds commonly used as preservatives in US-licensed vaccines were: phenol < 2-phenoxyethanol < benzethonium chloride < Thimerosal.
The observed relative toxicity indices (human neuroblastoma cells/bacterial cells) were: 2-phenoxyethanol (4.6-fold) < phenol (12.2-fold) < Thimerosal (>330-fold). In addition, for the compounds tested, except for 2- phenoxyethanol, the concentrations necessary to induce significant killing of bacterial cells were significantly higher than those routinely present in US-licensed vaccine/biological preparations. These investigators concluded, “(f)uture formulations of US[-]licensed vaccines/biologics should be produced in aseptic manufacturing plants as single dose preparations, eliminating the need for preservatives
and an unnecessary risk to patients.”
Using human neuroblastoma cells, this study showed that the relative toxicities of the compounds commonly used as preservatives in US-licensed vaccines were: phenol < 2-phenoxyethanol < benzethonium chloride < Thimerosal.
The observed relative toxicity indices (human neuroblastoma cells/bacterial cells) were: 2-phenoxyethanol (4.6-fold) < phenol (12.2-fold) < Thimerosal (>330-fold). In addition, for the compounds tested, except for 2- phenoxyethanol, the concentrations necessary to induce significant killing of bacterial cells were significantly higher than those routinely present in US-licensed vaccine/biological preparations. These investigators concluded, “(f)uture formulations of US[-]licensed vaccines/biologics should be produced in aseptic manufacturing plants as single dose preparations, eliminating the need for preservatives
and an unnecessary risk to patients.”
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A document supporting the safety claims of some of the vaccines and some suggestive evidence indicating there is no link between autism and specific vaccines. A question to ask when reading all of these documents are who funded the research? Research is one of the most manipulative models to alter an industry in favor or against something to support a select few corporate interests.
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Below is an article written by the CDC in 2010 detailing the ingredients contained within some of the leading vaccines on the market today with the reasoning for the ingredients and which vaccines contain which.
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Must-See Videos:
- The Greater Good Documentary
- Dr. Roby Mitchell, MD - H1N1 Vaccine Does Not Work People Used As Human Guinea Pigs
- Doctor Admits H1N1 Vaccine Is More Dangerous Than Swine Flu Itself & Will Not Give It To His Kids
- Merck Vaccine Expert tells Truth about Vaccine Dangers
- Vaccine Dangers Exposed Part 1 Of 3
- Vaccine Dangers Exposed Part 2 Of 3
- Vaccine Dangers Exposed Part 3 of 3
- The Risks of the Whooping Cough Vaccine
- Thinking About a Flu Shot? Watch This First! Part 1 of 3
- Thinking About a Flu Shot? Watch This First! Part 2 of 3
- Thinking About a Flu Shot? Watch This First! Part 3 of 3
- Flu and its Vaccine: What's coming through that needle? (Outstanding Presentation by. Dr. Sherri Tenpenny Hour Long)
- Leaked Pentagon Video Shows Vaccine Designed to Modify Behavior (Disturbing to say the least)
Are these ingredients safe?
(DISCLAIMER: Keep in mind that there are different forms of each of these ingredients and delivery (ingestion, intra-muscular, inhalation, etc.) all have different effects. Just because studies that show aluminum hydroxide is poisonous via ingestion doesn't mean it's as poisonous as intramuscular injection or vice versa? We do not know all the reactions. We just know there are a lot of documents you all should be aware exist and abstracts that raise concern!
Diphtheria, Pertussis, Rubella, Tetanus Vaccines Not Specific To 1 Ingredient Abstracts:
Aluminum hydroxide: Common adjuvant in the following vaccines Anthrax (BioThrax), DTaP (Infanrix), DTaP-Hep B-IPV (Pediarix), DT (Massacusetts), Td (Massachusetts), Hepatitis A (Havrix), Hepatits A-Hepatits B (Twinrix), Hepatits B (Engerix-B)
Benzethonium Chloride: Common preservative in the following vaccine Anthrax (BioThrax) {note worthy}
Brilliant Green: Common excipient that acts as a dye in the following vaccines Vaccinia (Dryvax-historic)
Formaldehyde, formalin: Common excipient that acts as a antimicrobial & preservative in the following vaccines Anthrax (BioThrax), DTaP (all brands), DTaP-Hep B-IPV (Pediarix), DT (all brands), Td (all brands), Hepatitis A (Havrix, Vaqta), Hepatits A-Hepatits B (Twinrix), Hib (ActHIB), Hib-Hepatits B (Comvax), Influenza (Fluzone), Japanese encephalitis (JE-Vax), Poliovirus inactivated (Ipol)
Monosodium Glutamate: Common excipient that acts as a stabilizer in the following vaccines Influenza (FluMist), Varicella (Varivax)
Phenol, 2-phenoxyethanol (EGPE), benzethonium chloride: Common excipient that acts as a preservative in the following vaccines/tests Mantoux tuberculin skin test (TST) (also known as the Mantoux screening test, Tuberculin Sensitivity Test, Pirquet test, or PPD test for Purified Protein Derivative)
Polysorbate 80, tween 80: Common excipient that acts as a surfactant in the following vaccines DTaP (Infanrix, Tripedia), DTaP-Hep B-IPV (Pediarix)
Squalene, MF59: Common component that acts as a immune-stimulater in the following vaccines influenza vaccine (FLUAD, Chiron), other sources unknown?
Thimerosal, mercury (Hg): Common excipient that acts as a preservative in the following vaccines DTaP (some multidose containers), DT (some multidose containers), Td (some multidose containers), Hepatits B (some multidose containers), Hib (some multidose containers), Influenza (some multidose containers), Japanese encephalitis (JE-Vax), Meningococcal (Menomune), Rabies (BioRab). Some singledose containers contain trace amounts of thimerosal form the production process, but substantially lower concentrations than if used as a preservative. Consult product monographs and labeling for details.
- Chronic arthritis after rubella vaccination.
- Delay in diphtheria, pertussis, tetanus vaccination is associated with a reduced risk of childhood asthma.
Aluminum hydroxide: Common adjuvant in the following vaccines Anthrax (BioThrax), DTaP (Infanrix), DTaP-Hep B-IPV (Pediarix), DT (Massacusetts), Td (Massachusetts), Hepatitis A (Havrix), Hepatits A-Hepatits B (Twinrix), Hepatits B (Engerix-B)
- Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration.
- Aluminum adjuvant linked to Gulf War illness induces motor neuron death in mice.
- Long-term persistence of vaccine-derived aluminum hydroxide is associated with chronic cognitive dysfunction.
- Macrophagic myofasciitis lesions assess long-term persistence of vaccine-derived aluminium hydroxide in muscle.
- Macrophagic myofasciitis in children is a localized reaction to vaccination.
- Safety and immunogenicity of inactivated, Vero cell culture-derived whole virus influenza A/H5N1 vaccine given alone or with aluminum . . .
- Macrophagic Myofaciitis a Vaccine (alum) Autoimmune-Related Disease.
- Aluminum hydroxide intake: real risk of aluminum toxicity.
- Aluminum-adjuvanted vaccines transiently increase aluminium levels in murine brain tissue.
- [Lessons from macrophagic myofasciitis: towards definition of a vaccine adjuvant-related syndrome].
- Adverse Effects of Pertussis and Rubella Vaccines
- [Aluminum as an adjuvant in vaccines and post-vaccine reactions].
- [Aluminum allergy caused by DTP vaccine].
- Alumina nanoparticles induce expression of endothelial cell adhesion molecules.
- Polyglandular autoimmunity with macrophagic myofasciitis.
- Atypical presentation of macrophagic myofasciitis 10 years post vaccination.
- AlOH3-adjuvanted vaccine-induced macrophagic myofasciitis in rats is influenced by the genetic background.
- Blood oxidative stress status in patients with macrophagic myofasciitis.
- [Macrophagic myofasciitis: inflammatory, vaccination-associated muscular disease].
- Inflammatory myopathy with abundant macrophages (IMAM): a condition sharing similarities with cytophagic histiocytic panniculitis . . .
- Macrophagic myofasciitis: a summary of Dr. Gherardi's presentations.
Benzethonium Chloride: Common preservative in the following vaccine Anthrax (BioThrax) {note worthy}
- The relative toxicity of compounds used as preservatives in vaccines and biologics. (Well worth reading, also a thimerosal abstract)
- Adverse effects by artificial grapefruit seed extract products in patients on warfarin therapy.
- Cationic surfactants induce apoptosis in normal and cancer cells.
Brilliant Green: Common excipient that acts as a dye in the following vaccines Vaccinia (Dryvax-historic)
- The potential for human exposure, direct and indirect, to the suspected carcinogenic triphenylmethane dye Brilliant Green from green . . .
- [Toxicogenetic effects of azo- and arylmethane dyes].
Formaldehyde, formalin: Common excipient that acts as a antimicrobial & preservative in the following vaccines Anthrax (BioThrax), DTaP (all brands), DTaP-Hep B-IPV (Pediarix), DT (all brands), Td (all brands), Hepatitis A (Havrix, Vaqta), Hepatits A-Hepatits B (Twinrix), Hib (ActHIB), Hib-Hepatits B (Comvax), Influenza (Fluzone), Japanese encephalitis (JE-Vax), Poliovirus inactivated (Ipol)
- Adjuvant effects of gaseous formaldehyde on the hyper-responsiveness and inflammation in a mouse asthma model immunized by ovalbumin.
- Formaldehyde induces neurotoxicity to PC12 cells involving inhibition of paraoxonase-1 expression and activity.
- [Effect of formaldehyde on energy metabolism in postnatal rat cortex neurons in culture].
- Formalin toxicity in hydatid liver disease.
- Formaldehyde and leukemia: epidemiology, potential mechanisms, and implications for risk assessment.
- Formaldehyde cytotoxicity in three human cell types assessed in three different assays.
- Toxicity of formaldehyde to human oral fibroblasts and epithelial cells: influences of culture conditions and role of thiol status. (tooth compsites)
- Studies of inspiratory airflow patterns in the nasal passages of the F344 rat and rhesus monkey using nasal molds: relevance to formaldehyde toxicity.
- Formaldehyde toxicity. Part I. Occupational exposure and a report of 5 cases.
- Formaldehyde toxicity. Part II. Review of acute and chronic effects on health.
- Beware of formaldehyde in disguise.
- Tumor tissue-derived formaldehyde and acidic microenvironment synergistically induce bone cancer pain.
- [Cancer risk assessment in a group of traffic officers].
- Association between six environmental chemicals and lung cancer incidence in the United States.
- Occupational exposure to formaldehyde: genotoxic risk evaluation by comet assay and micronucleus test using human peripheral lymphocytes.
- Reproductive and developmental toxicity of formaldehyde: A systematic review.
- Effects of long-term low-dose formaldehyde exposure on global genomic hypomethylation in 16HBE cells.
- Effect of formaldehyde on cell proliferation and death.
- Final Report on Carcinogens Background Document for Formaldehyde. (lengthy report)
- Genotoxic effects in occupational exposure to formaldehyde: A study in anatomy and pathology laboratories and formaldehyde-resins production.
- Occupational exposure to formaldehyde, hematotoxicity, and leukemia-specific chromosome changes in cultured myeloid progenitor cells.
Monosodium Glutamate: Common excipient that acts as a stabilizer in the following vaccines Influenza (FluMist), Varicella (Varivax)
- Foreign body granuloma caused by monosodium glutamate after BCG vaccination.
- Monosodium glutamate versus diet induced obesity in pregnant rats and their offspring.
- Glutamate receptors, neurotoxicity and neurodegeneration.
- Effect of dietary monosodium glutamate on HFCS-induced hepatic steatosis: expression profiles in the liver and visceral fat.
Phenol, 2-phenoxyethanol (EGPE), benzethonium chloride: Common excipient that acts as a preservative in the following vaccines/tests Mantoux tuberculin skin test (TST) (also known as the Mantoux screening test, Tuberculin Sensitivity Test, Pirquet test, or PPD test for Purified Protein Derivative)
- Stimulation of suicidal erythrocyte death by benzethonium.
- Benzethonium increases the cytotoxicity of S(+)-ketamine in lymphoma, neuronal, and glial cells.
- Effects of ethylene glycol ethers on cell viability in the human neuroblastoma SH-SY5Y cell line.
- In vitro induction of apoptosis vs. necrosis by widely used preservatives: 2-phenoxyethanol, a mixture of isothiazolinones, imida . . .
- 2-Phenoxyethanol: a neurotoxicant?
- Hemolytic activity of ethylene glycol phenyl ether (EGPE) in rabbits.
- Assessment of ethylene glycol monobutyl and monophenyl ether reproductive toxicity using a continuous breeding protocol in Swiss CD-1 mice.
Polysorbate 80, tween 80: Common excipient that acts as a surfactant in the following vaccines DTaP (Infanrix, Tripedia), DTaP-Hep B-IPV (Pediarix)
- Polysorbate 80 in medical products and nonimmunologic anaphylactoid reactions.
- [Polysorbate-80 modified neurotoxin nanoparticle with its transport and cytotoxicity against blood-brain barrier].
- Hypersensitivity reactions to the polysorbate contained in recombinant erythropoietin and darbepoietin.
- In vitro toxicity of surfactants in U937 cells: cell membrane integrity and mitochondrial function.
- Early acute hepatitis with parenteral amiodarone: a toxic effect of the vehicle?
- Toxic susceptibilities in the newborn with special consideration of polysorbate toxicity.
- Bioassay of b-TGdR for possible carcinogenicity.
- [Toxic effects of Tween 60 and 80 on thrombocytes (spindle cells) in frog blood].
- Flow-cytometric analysis on adverse effects of polysorbate 80 in rat thymocytes.
- Influence of surface-active food additives on the integrity and permeability of rat intestinal mucosa.
- Delayed effects of neonatal exposure to Tween 80 on female reproductive organs in rats.
- [Anaphylactoid reactions induced by polysorbate 80 on Beagle dogs].
Squalene, MF59: Common component that acts as a immune-stimulater in the following vaccines influenza vaccine (FLUAD, Chiron), other sources unknown?
- Autoimmune hemolytic anemia following MF59-adjuvanted influenza vaccine administration: a report of two cases.
- Autoimmunity induced by adjuvant hydrocarbon oil components of vaccine.
- Induction of lupus autoantibodies by adjuvants.
- Antibodies to squalene in Gulf War syndrome.
- Adverse events following pandemic A (H1N1) 2009 monovalent vaccines in pregnant women--Taiwan. (pro vac but concerning results nonetheless)
Thimerosal, mercury (Hg): Common excipient that acts as a preservative in the following vaccines DTaP (some multidose containers), DT (some multidose containers), Td (some multidose containers), Hepatits B (some multidose containers), Hib (some multidose containers), Influenza (some multidose containers), Japanese encephalitis (JE-Vax), Meningococcal (Menomune), Rabies (BioRab). Some singledose containers contain trace amounts of thimerosal form the production process, but substantially lower concentrations than if used as a preservative. Consult product monographs and labeling for details.
- Integrating experimental (in vitro and in vivo) neurotoxicity studies of low-dose thimerosal relevant to vaccines.
- Hair mercury in breast-fed infants exposed to thimerosal-preserved vaccines.
- Exposure to mercury during the first six months via human milk and vaccines: modifying risk factors.
- Persistent behavioral impairments and alterations of brain dopamine system after early postnatal administration of thimerosal in rats.
- Thimerosal induces apoptosis in a neuroblastoma model via the cJun N-terminal kinase pathway.
- Thimerosal induces neuronal cell apoptosis by causing cytochrome c and apoptosis-inducing factor release from mitochondria.
- Thimerosal induces DNA breaks, caspase-3 activation, membrane damage, and cell death in cultured human neurons and fibroblasts.
- Comparison of organic and inorganic mercury distribution in suckling rat.
- Thimerosal distribution and metabolism in neonatal mice: comparison with methyl mercury.
- Lasting neuropathological changes in rat brain after intermittent neonatal administration of thimerosal.
- Mitochondrial mediated thimerosal-induced apoptosis in a human neuroblastoma cell line (SK-N-SH).
- Effects of thimerosal on NGF signal transduction and cell death in neuroblastoma cells.
- Thimerosal neurotoxicity is associated with glutathione depletion: protection with glutathione precursors.
- Neurotoxic effects of postnatal thimerosal are mouse strain dependent.
- Gender-selective toxicity of thimerosal.
- Making sense of epidemiological studies of young children exposed to thimerosal in vaccines.
- Induction of metallothionein in mouse cerebellum and cerebrum with low-dose thimerosal injection.
- Genotoxicity of thimerosal in cultured human lymphocytes with and without metabolic activation sister chromatid exchange analysis proli . . .
- Thiol-modulated mechanisms of the cytotoxicity of thimerosal and inhibition of DNA topoisomerase II alpha.
- Evaluation of cytotoxicity attributed to thimerosal on murine and human kidney cells.
- An assessment of downward trends in neurodevelopmental disorders in the United States following removal of Thimerosal from childhood . . .
- Mercury and autism: accelerating evidence?
- Effect of thimerosal, a preservative in vaccines, on intracellular Ca2+ concentration of rat cerebellar neurons.
- Biochemical and molecular basis of thimerosal-induced apoptosis in T cells: a major role of mitochondrial pathway.
- Thimerosal induces toxic reaction in non-sensitized animals.
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Vaccine Refusal & Exemption Forms
* As seen on Dr. Tenpenny's website
Childcare and School Immunization Requirements This 39 page pdf contains State immunization policies that were validated in August, 2006. Document reflects state laws, regulations, or rules for vaccination requirements for enrollment and/or attendance in day care, Head Start, kindergarten, grades 1 through 12, colleges, and universities. Some maps are included for comparison purposes.
- Hep B vaccine in hospital for newborn refusal, sample (pdf)
- TB testing refusal, sample (pdf)
- OSHA Declination Statement Form (also, pdf)
- Religious exemption letter that was approved in Florida (Word) (pdf)
- School Vaccine Exemption Form, sample (Word) (pdf)
- Affidavit for Parents with International Adoption (Word) (pdf)
- State Immunization Laws Searchable Database This tool contains results from a 50-state legislative review of laws requiring assessment of vaccination status and vaccine administration for healthcare workers and patients/residents. The review was conducted by CDC in 2005 and collected data on laws for the following types of facilities: hospitals, ambulatory care facilities, individual providers' practices, correctional facilities, and facilities for the developmentally disabled.
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Quotes from the Medical Community Regarding Vaccine Concerns
"My suspicion, which is shared by others in my profession, is that the nearly 10,000 SIDS deaths that occur in the United States each year are related to one or more of the vaccines that are routinely given children. The pertussis vaccine is the most likely villain, but it could also be one or more of the others."
Dr. Mendelsohn, M.D.
"The evidence for indicting immunisations for SIDS is circumstantial, but compelling. However, the keepers of the keys to medical-research funds are not interested in researching this very important lead to the cause of an ongoing, and possibly preventable, tragedy. Anything that implies that immunisations are not the greatest medical advance in the history of public health is ignored or ridiculed. Can you imagine the economic and political import of discovering that immunisations are killing thousands of babies?"
Dr. Douglass M.D.
"Only after realising that routine immunisations were dangerous did I achieve a substantial drop in infant death rates. The worst vaccine of all is the whooping cough vaccine... it is responsible for a lot of deaths and for a lot of infants suffering irreversible brain damage. In susceptible infants, it knocks their immune systems about, leading to irreparable brain damage, or severe attacks or even deaths from diseases like pneumonia or gastro-enteritis and so on."
Dr. Kalokerinos, M.D.
"Delay of DPT immunisation until 2 years of age in Japan has resulted in a dramatic decline in adverse side effects. In the period of 1970-1974, when DPT vaccination was begun at 3 to 5 months of age, the Japanese national compensation system paid out claims for 57 permanent severe damage vaccine cases, and 37 deaths. During the ensuing six year period 1975-1980, when DPT injections were delayed to 24 months of age, severe reactions from the vaccine were reduced to a total of eight with three deaths. This represents an 85 to 90 percent reduction in severe cases of damage and death."
Dr. Raymond Obomsawin, M.D.
"Autism may be a disorder linked to the disruption of the G-alpha protein, affecting retinoid receptors in the brain. A study of sixty autistic children suggests that autism may be caused by inserting a G-alpha protein defect, the pertussis toxin found in the D.P.T. vaccine, into genetically at-risk children."
Dr. Mary N. Megson, M.D.
"This report describes six mothers who received live virus vaccines and one who received a Hepatitis B vaccine during pregnancy after having received an MMR booster five months prior to conception. All the children who resulted from these pregnancies have had developmental problems, six out seven (85%) were diagnosed with autism, and the seventh seems to exhibit symptoms often associated with autistic spectrum disorders."
Dr. F. EdwardYazbak, M.D.
"This..forced me to look into the question of vaccination further, and the further I looked the more shocked I became. I found that the whole vaccine business was indeed a gigantic hoax. Most doctors are convinced that they are useful, but if you look at the proper statistics and study the instances of these diseases you will realise that this is not so . . . My final conclusion after forty years or more in this business [medicine] is that the unofficial policy of the World Health Organisation and the unofficial policy of the 'Save the Children's Fund' and ... [other vaccine promoting] organisations is one of murder and genocide. . . . I cannot see any other possible explanation. . . . You cannot immunise sick children, malnourished children, and expect to get away with it. You'll kill far more children than would have died from natural infection."
Dr. Kalokerinos M.D.
"The medical authorities keep lying. Vaccination has been a disaster on the immune system. It actually causes a lot of illnesses. We are changing our genetic code through vaccination."
Dr. Guylaine Lanctot M.D.
"There is insufficient evidence to support routine vaccination of healthy persons of any age."
Dr. Paul Frame M.D.
"My suspicion, which is shared by others in my profession, is that the nearly 10,000 SIDS deaths that occur in the United States each year are related to one or more of the vaccines that are routinely given children. The pertussis vaccine is the most likely villain, but it could also be one or more of the others."
Dr. Mendelsohn, M.D.
"The evidence for indicting immunisations for SIDS is circumstantial, but compelling. However, the keepers of the keys to medical-research funds are not interested in researching this very important lead to the cause of an ongoing, and possibly preventable, tragedy. Anything that implies that immunisations are not the greatest medical advance in the history of public health is ignored or ridiculed. Can you imagine the economic and political import of discovering that immunisations are killing thousands of babies?"
Dr. Douglass M.D.
"Only after realising that routine immunisations were dangerous did I achieve a substantial drop in infant death rates. The worst vaccine of all is the whooping cough vaccine... it is responsible for a lot of deaths and for a lot of infants suffering irreversible brain damage. In susceptible infants, it knocks their immune systems about, leading to irreparable brain damage, or severe attacks or even deaths from diseases like pneumonia or gastro-enteritis and so on."
Dr. Kalokerinos, M.D.
"Delay of DPT immunisation until 2 years of age in Japan has resulted in a dramatic decline in adverse side effects. In the period of 1970-1974, when DPT vaccination was begun at 3 to 5 months of age, the Japanese national compensation system paid out claims for 57 permanent severe damage vaccine cases, and 37 deaths. During the ensuing six year period 1975-1980, when DPT injections were delayed to 24 months of age, severe reactions from the vaccine were reduced to a total of eight with three deaths. This represents an 85 to 90 percent reduction in severe cases of damage and death."
Dr. Raymond Obomsawin, M.D.
"Autism may be a disorder linked to the disruption of the G-alpha protein, affecting retinoid receptors in the brain. A study of sixty autistic children suggests that autism may be caused by inserting a G-alpha protein defect, the pertussis toxin found in the D.P.T. vaccine, into genetically at-risk children."
Dr. Mary N. Megson, M.D.
"This report describes six mothers who received live virus vaccines and one who received a Hepatitis B vaccine during pregnancy after having received an MMR booster five months prior to conception. All the children who resulted from these pregnancies have had developmental problems, six out seven (85%) were diagnosed with autism, and the seventh seems to exhibit symptoms often associated with autistic spectrum disorders."
Dr. F. EdwardYazbak, M.D.
"This..forced me to look into the question of vaccination further, and the further I looked the more shocked I became. I found that the whole vaccine business was indeed a gigantic hoax. Most doctors are convinced that they are useful, but if you look at the proper statistics and study the instances of these diseases you will realise that this is not so . . . My final conclusion after forty years or more in this business [medicine] is that the unofficial policy of the World Health Organisation and the unofficial policy of the 'Save the Children's Fund' and ... [other vaccine promoting] organisations is one of murder and genocide. . . . I cannot see any other possible explanation. . . . You cannot immunise sick children, malnourished children, and expect to get away with it. You'll kill far more children than would have died from natural infection."
Dr. Kalokerinos M.D.
"The medical authorities keep lying. Vaccination has been a disaster on the immune system. It actually causes a lot of illnesses. We are changing our genetic code through vaccination."
Dr. Guylaine Lanctot M.D.
"There is insufficient evidence to support routine vaccination of healthy persons of any age."
Dr. Paul Frame M.D.
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"Either you run the day or the day runs you."
Jim Rohn
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All contents except quotations © 2009-2015 Body Epiphanies Massage & Nutrition
"Either you run the day or the day runs you."
Jim Rohn
______________________________________________________________________
All contents except quotations © 2009-2015 Body Epiphanies Massage & Nutrition