The current movement to remove vaccine exemptions

6/11/2015

Measles and Medical Tyranny

National Childhood Vaccine Injury Act in 1986

• Signed into law by Ronald Reagan after he and congress after heavy lobbying by pharmaceuticals to protect them from lawsuits rising from vaccines injuries and death

• Injured or killed by vaccine, you cannot legally sue the Pharmaceuticals, Physicians or Gov’t

• Removed any financial incentive to try and improve vaccine safety

• Created National Vaccine Compensation Injury Program (NVICP) in 1988

• To date NVICP has paid over 2.8 billion out for children and adults damaged or killed by a vaccine, over 3.1 billion with attorney fees

• Pay up to 250,000 for vaccine related death

• Funded by tax payer. 0.75 is charged for every vaccine patient receives

• Not Judged by jury of your peers or a judge. You are judged by 11 special masters

• Must prove you were injured by vaccine, fighting the government

http://www.hrsa.gov/vaccinecompensation/index.htmlhttp://www.hrsa.gov/vaccinecompensation/statisticsreport.pdf

 Vaccine Adverse Event Reporting System (VAERS)

• Sponsored by the FDA

• Health care personnel are required by law to report adverse reactions due to vaccines

• Anyone can report adverse reaction to VAERS

• Problem, Physicians and health care workers are taught vaccines are safe and effective and do not look for any connection

https://vaers.hhs.gov/indexhttp://www.nvic.org/injury-compensation.aspx

• Only 1% of serious adverse reactions are reported according to Dr. David Kessler, former head of FDA

http://www.fda.gov/downloads/Safety/MedWatch/UCM201419.pdf

http://www.supremecourt.gov/opinions/10pdf/09-152.pdf

OCTOBER TERM, 2010, SUPREME COURT OF THE UNITED STATESBRUESEWITZ ET AL. v. WYETH LLC, FKA WYETH, INC.,

• Parents of Hanna Bruesewitz sued Wyeth Pharmaceuticals for vaccine damage from DTP produced by Wyeth for defective design

• Supreme court ruled that you cannot sue because of rules set up in NVICP

• Supreme court ruled that Vaccines are “Unavoidably Unsafe”

• Vaccines are the only product in the world that are allowed to be defective and cause damage and death and the right to sue your physician who recommends and administers the vaccine, the pharmaceuticals who produce the vaccine or the Government who mandates it was stripped from us when the National Childhood Vaccine Injury Act signed into law by President Reagan.

• What happens when 30 people become sick from spinach infected with e. coli or Listeria? All of the product is recalled and destroyed.

• What happens when thousands of children every year are injured, develop chronic illness like asthma, autoimmune disease, allergies, autism, ADD, ADHD and even death as a result of vaccination? They are all ignored as if they do not exist. Just look at the epidemics of all of these disease in the last 30 years when we went from 24 vaccines in 1980 during the first 18 years to 49 vaccines during the first 6 years of life.

AMA MEDICAL ETHICS

Opinion 8.082 - Withholding Information from Patients

Withholding medical information from patients without their knowledge or consent is ethically unacceptable.http://www.ama-assn.org/ama/pub/physician-resources/medical-ethics/code-medical-ethics/opinion8082.page

Opinion 8.08 – Informed ConsentThe patient should make his or her own determination about treatment. The physician's obligation is to present the medical facts accurately to the patient or to the individual responsible for the patient’s care and to make recommendations for management in accordance with good medical practice. The physician has an ethical obligation to help the patient make choices from among the therapeutic alternatives consistent with good medical practice. Informed consent is a basic policy in both ethics and law that physicians must honor, unless the patient is unconscious or otherwise incapable of consenting and harm from failure to treat is imminent.

http://www.ama-assn.org/ama/pub/physician-resources/medical-ethics/code-medical-ethics/opinion808.page?

NUREMBERG CODE: LAW #10 - VOLUNTARY CONSENT

1. The voluntary consent of the human subject is absolutely essential. http://www.hhs.gov/ohrp/archive/nurcode.html

Opinion 9.133 Routine Universal Immunization of Physicians

In the context of a highly transmissible disease that poses significant medical risk for vulnerable patients or colleagues, or threatens the availability of the health care workforce, particularly a disease that has potential to become epidemic or pandemic, and for which there is an available, safe, and effective vaccine, physicians have an obligation to: 

(a) Accept immunization absent a recognized medical, religious, or philosophic reason to not be immunized. 

adopted November 2010.http://www.ama-assn.org/ama/pub/physician-resources/medical-ethics/code-medical-ethics/opinion9133.page

Now after 100 years the AMA has announced on 6-9-2015 to oppose religious and philosophical exemptions and only allow medical exemption while physicians get to refuse a vaccination for medical, philosophical or religious reasons as stated above in their code of ethics. "Under new policy, the AMA will seek more stringent state immunization requirements to allow exemptions only for medical reasons," the organization said in a press release.http://www.forbes.com/sites/brucejapsen/2015/06/08/ama-end-personal-religious-vaccination-exemptions/ and for an in depth article on AMA code of ethics and large work groups and unions that oppose mandatory vaccinationhttp://www.nvic.org/NVIC-Vaccine-News/August-2012/labor-unions-oppose-mandatory-flu-shots-as-ama-che.aspx

VACCINE EXEMPTIONS

• NO VACCINES = NO SCHOOL = NOT TRUE

• 50 states allow a medical vaccine exemption

• 48 states allow a religious vaccine exemption

• 17 states allow a philosophical, conscientious or personal belief exemption.

• These are the exemptions that the bought federal and state politicians are trying to eliminate

http://www.generationrescue.org/resources/vaccination/exemption-laws-by-state-2/

NBC Survey Finds Congress is Unanimous on Vaccinations

Only 28% stated they vaccinated. And this is unanimous? Others hid behind obvious answers like

No response, No answer, No kids and I say NO reporting integrity was involved in this article. More

media propaganda because 70% of revenues come from Big Pharma Ads http://edgytruth.com/2015/06/09/here-is-proof-that-big-pharma-buys-the-media-its-disgusting/

http://www.nbcnews.com/politics/politics-news/nbc-survey-finds-congress-unanimous-vaccinations-n301831

Oregon Senator Elizabeth Steiner Hayward

• Wants to exercise her right to medical choice and eliminate your right to medical choice

• Has MS, went against her Doctor telling her not to breast feed because we need to start you on interferon, May 2012

http://healthimpactnews.com/2015/medical-tyranny-in-action-in-oregon-doctor-and-senator-wants-medical-freedom-for-herself-but-not-oregon-citizens/

http://www.aafp.org/news/inside-aafp/20120502steinerhayward.html

Nearly 300 Vaccines Are in Development; Research Focuses on Prevention and Treatment

• There are 271 vaccines in current development.

• 15 for allergies• 99 for cancer• 137 for infectious diseases• 10 for neurological disorders• 13 for otherhttp://www.phrma.org/sites/default/files/pdf/Vaccines_2013.pdf

http://vaccineliberationarmy.com/2013/04/05/poster-comparing-1940-1980-and-2012-childrens-vaccine-schedule-2/

http://www.sott.net/article/292272-A-century-later-Gandhis-Anti-Vaccine-views-ring-true

http://www.naturalnews.com/048806_vaccine_petition_White_House_fraud.html

http://org.salsalabs.com/o/568/p/dia/action/public/?action_KEY=11690

Dr. Rima’s Petition to congress members and the White House

http://www.usatoday.com/story/opinion/2015/01/29/vaccination-parenting-children-your-say-interactive/22557363/

The Federal and State politicians are completely bought and paid for by Monsanto and the Pharmaceutical corporations as they do not listen to their constituents when money and power speaks louder than their concern for what the people want.

Measles • Immune system is immature and is trying to organize and develop the first two years

• Optimum time to acquire measles naturally is age 5-9

• Measles vaccine wanes after several years. Boosters provide less immune response

• All vaccines cause imbalance in TH1 (cellular T cells: phagocytes, antigen specific T-lymphocytes) And TH2 (humoral T cells: antibody) arms of the immune system. Overstimulation of this part of the adaptive immune system provokes allergies, asthma, and auto-immune diseases.

• Vaccine is shifting the age groups that should acquire the diseases from 5-9 to infants and adults where complications can occur testicular and ovarian cancer in adults, neurological in both groups and atypical measles

• The benefits of having measles at the right age (5-9) 1) Provides lifelong immunity to it 2) measles strengthens and helps mature a child’s helper T-cell adaptive immune system, and most importantly its cancer-preventing Th1 side.http://www.lewrockwell.com/2015/02/donald-w-miller-jr-md/more-dangerous-than-measles/

• "Infection with mumps may lead to enhanced immunity against ovarian cancer."http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2951028/

• Child mortality is 200-400 times greater in undeveloped countries due to malnourishment Dissolving Illusions, disease, vaccines and the forgotten history, page 340

http://www.cdc.gov/measles/cases-outbreaks.html

• CDC claims Measles was eradicated in 2000. Look at chart. Measles was never was eradicated

http://www.cdc.gov/measles/vaccination.html

• 644 cases of Measles in 2014 and not a word in the media. 54 cases from Disney Land and now terms like death and dangerous are used

• CDC claims 1/1,000 will have encephalitishttp://www.cdc.gov/measles/cases-outbreaks.html

• Reality is 1/10,000 may contract encephalitisDr. Robert Mendelsohn, MD, “How to raise a healthy child in spite of your doctor”, pg. 236-237

• 65% decrease in mortality of children who were given two doses of 200,000 IU of vitamin A compared to placebo. (Approved by WHO)

• Again Nutrition is the Key NOT VACCINEShttp://www.ncbi.nlm.nih.gov/m/pubmed/11869601/

Vaccine is Edmonston-Enders which is type A strain (genotype) http://www.cdc.gov/vaccines/pubs/pinkbook/meas.html

Of the first 54 cases, 6 were vaccinated. 2 had one dose and 4 had two or more doses of MMR.

All cases in outbreak is B3 strain, not the Edmonton strain, so vaccine is much less effective against this different strain

http://emergency.cdc.gov/han/han00376.asp

http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM123796.pdf

5.8 Risk of Vaccine Virus Transmission Post-licensing experience with VARIVAX suggests that transmission of varicella vaccine virus may occur between healthy vaccine recipients (who develop or do not develop a varicella-like rash) and contacts susceptible to varicella, as well as high-risk individuals susceptible to varicella.

Vaccine recipients should attempt to avoid, to the extent possible, close association with high-risk individuals susceptible to varicella for up to 6 weeks following vaccination

Excretion of small amounts of the live, attenuated rubella virus from the nose or throat hasoccurred in the majority of susceptible individuals 7 to 28 days after vaccination 

ProQuad (MMRV) Vaccine Insert

Body as a Whole: Panniculitis; atypical measles; fever; syncope; headache; dizziness; malaise; irritability. Cardiovascular System: Vasculitis. Digestive System: Pancreatitis; diarrhea; vomiting; parotitis; nausea. Endocrine System: Diabetes mellitus. Hemic and Lymphatic System: purpura; regional lymphadenopathy; leukocytosis. Immune System: Anaphylaxis and anaphylactoid reactions have been reported as well as related phenomena such as angioneurotic edema (including peripheral or facial edema) and bronchial spasm in individuals with or without an allergic history. Musculoskeletal System: Arthritis; arthralgia; myalgia

http://www.merck.com/product/usa/pi_circulars/m/mmr_ii/mmr_ii_pi.pdf

1 M-M-R® II(MEASLES, MUMPS, and RUBELLA VIRUS VACCINE LIVE) DESCRIPTION M-M-R® II(Measles, Mumps, and Rubella Virus Vaccine Live) is a live virus vaccine for vaccination against measles (rubeola), mumps, and rubella (German measles). M-M-R IIis a sterile lyophilized preparation of (1) ATTENUVAX® (Measles Virus Vaccine Live), a more attenuated line of measles virus, derived from Enders' attenuated Edmonston strain and propagated in chick embryo cell culture; (2) MUMPSVAX®(Mumps Virus Vaccine Live), the Jeryl Lynn™ (B level) strain of mumps virus propagated inchick embryo cell culture; and (3) MERUVAX® II(Rubella Virus Vaccine Live), the Wistar RA27/3 strain of live attenuated rubella virus propagated in WI-38 human diploid lung fibroblasts.{1,2} The growth medium for measles and mumps is Medium 199 (a buffered salt solution containing vitamins and amino acids and supplemented with fetal bovine serum) containing SPGA (sucrose, phosphate, glutamate, and recombinant human albumin) as stabilizer and neomycin.The growth medium for rubella is Minimum Essential Medium (MEM) [a buffered salt solution containing vitamins and amino acids and supplemented with fetal bovine serum] containing recombinant human albumin and neomycin. Sorbitol and hydrolyzed gelatin stabilizer are added to the individual virus harvests.The cells, virus pools, and fetal bovine serum are all screened for the absence of adventitious agents.The reconstituted vaccine is for subcutaneous administration. Each 0.5 mL dose contains not less than 1,000 TCID50(tissue culture infectious doses) of measles virus; 12,500 TCID50of mumps virus; and 1,000 TCID50of rubella virus. Each dose of the vaccine is calculated to contain sorbitol (14.5 mg), sodium phosphate, sucrose (1.9 mg), sodiumchloride, hydrolyzed gelatin (14.5 mg), recombinant human albumin (≤0.3 mg), fetal bovine serum (<1 ppm), other buffer and media ingredients and approximately 25 mcg of neomycin. The product contains no preservative. Before reconstitution, the lyophilized vaccine is a light yellow compact crystalline plug. M-M-R II, when reconstituted as directed, is clear yellow. CLINICAL PHARMACOLOGY Measles, mumps, and rubella are three common childhood diseases, caused by measles virus, mumps virus (paramyxoviruses), and rubella virus (togavirus), respectively, that may be associated with serious complications and/or death. For example,pneumonia and encephalitis are caused by measles. Mumps is associated with aseptic meningitis, deafness and orchitis; and rubella during pregnancy may cause congenital rubella syndrome in the infants of infected mothers. The impact of measles, mumps, and rubella vaccination on the natural history of each disease in the United States can be quantified by comparing the maximum number of measles, mumps, and rubella cases reported in a given year prior to vaccine use to the number of cases of each disease reported in 1995. For measles, 894,134 cases reported in 1941 compared to 288 cases reported in 1995 resulted in a 99.97% decrease in reported cases; for mumps, 152,209 cases reported in 1968 compared to 840 cases reported in 1995 resulted in a 99.45% decrease in reported cases; and for rubella, 57,686 cases reported in 1969 compared to 200 cases reported in 1995 resulted in a 99.65% decrease.{3} Clinical studies of 284 triple seronegative children,11 months to 7 years of age, demonstrated that M-M-R IIis highly immunogenic and generally well tolerated. In these studies, a single injection of the vaccine induced measles hemagglutination-inhibition (HI) antibodies in 95%, mumps neutralizing antibodies in 96%, and rubella HI antibodies in 99% of susceptible persons. However, a small percentage (1-5%) of vaccinees may fail to seroconvert after the primary dose (see also INDICATIONS AND USAGE,Recommended Vaccination Schedule). A study{4} of 6-month-old and 15-month-old infants born to vaccine-immunized mothers demonstrated that, following vaccination with ATTENUVAX, 74% of the 6-month-old infants developed detectable neutralizing antibody (NT) titers while 100% of the 15-month-old infants developed NT. This rate of seroconversion is higher than that previously reported for 6-month-old infants born to naturally immune mothers tested by HI assay. When the 6-month-old infants of immunized mothers were revaccinated at 2 15 months, they developed antibody titers equivalent to the 15-month-old vaccinees. The lower seroconversion rate in 6-month-olds has two possible explanations: 1) Due to the limit of the detection level of the assays (NT and enzyme immunoassay [EIA]), the presence of trace amounts of undetectable maternal antibody might interfere with the seroconversion of infants; or 2)The immune system of 6-month-olds is not always capable of mounting a response to measles vaccine as measured by the two antibody assays. There is some evidence to suggest that infants who are born to mothers who had wild-type measles and who are vaccinated at less than one year of age may not develop sustained antibody levels when later revaccinated. The advantage of early protection must be weighed against the chance for failure to respond adequately on reimmunization.{5,6} Efficacy of measles, mumps, and rubella vaccines was established in a series of double-blind controlled field trials which demonstrated a high degree ofprotective efficacy afforded by the individual vaccine components.{7-12} These studies also established that seroconversion in response to vaccination against measles, mumps, and rubella paralleled protection from these diseases.{13-15} Following vaccination, antibodies associated withprotection can be measured by neutralization assays, HI, or ELISA (enzyme linked immunosorbent assay) tests. Neutralizing and ELISA antibodies to measles, mumps, and rubella viruses are still detectable in most individuals 11 to 13 years after primary vaccination.{16-18} See INDICATIONS AND USAGE, Non-Pregnant Adolescent and Adult Females, for Rubella Susceptibility Testing. The RA 27/3 rubella strain in M-M-R IIelicits higher immediate post-vaccination HI, complement-fixing and neutralizing antibody levels than other strains of rubella vaccine{19-25} and has been shown to induce a broader profile of circulating antibodiesincluding anti-theta and anti-iota precipitating antibodies.{26,27} The RA 27/3 rubella strain immunologically simulates natural infection more closely than other rubella vaccine viruses.{27-29} The increased levels and broader profile of antibodies produced by RA 27/3 strain rubella virus vaccine appear tocorrelate with greater resistance to subclinical reinfection with the wild virus,{27,29-31} and provide greater confidence for lasting immunity. INDICATIONS AND USAGE Recommended Vaccination Schedule M-M-R IIis indicated for simultaneous vaccination against measles, mumps, and rubella in individuals 12 months of age or older. Individuals first vaccinated at 12 months of age orolder should be revaccinated prior to elementary school entry. Revaccination is intended to seroconvert those who do not respond to the first dose. The Advisory Committee on Immunization Practices (ACIP)recommends administration of the first dose of M-M-R II at 12 to 15 months of age and administration of the second dose of M-M-R IIat 4 to 6 years of age.{32} In addition, some public health jurisdictions mandate the age for revaccination. Consult the complete text of applicable guidelines regarding routine revaccination including that of high-risk adult populations. Measles Outbreak Schedule Infants Between 6 to 12 Months of Age Local health authorities may recommend measles vaccination of infants between 6 to 12 months of age in outbreak situations. This population may fail torespond to the components of the vaccine. Safety and effectiveness of mumps and rubella vaccine in infants less than 12 months of age have not been established. The younger the infant, the lower the likelihood of seroconversion (see CLINICAL PHARMACOLOGY). Such infants should receive a second dose of M-M-R IIbetween 12 to 15 months of age followed by revaccination at elementary school entry.{32} Unnecessary doses of a vaccine are best avoided by ensuring that written documentation of vaccination is preserved and a copy given to each vaccinee's parent or guardian. Other Vaccination Considerations Non-Pregnant Adolescent and Adult Females Immunization of susceptible non-pregnant adolescentand adult females of childbearing age with live attenuated rubella virus vaccine is indicated if certain precautions are observed (see below and PRECAUTIONS). Vaccinating susceptible postpubertal females confers individual protection against subsequently acquiring rubella infection during pregnancy, which in turn prevents infection of the fetus and consequent congenital rubella injury.{33} 3 Women of childbearing age should be advised not to become pregnant for 3 months after vaccination and should be informed of the reasons for this precaution. The ACIP has stated "If it is practical and if reliable laboratory services are available, women of childbearing age who are potential candidates for vaccination can have serologic tests to determine susceptibility to rubella. However, with the exception of premarital and prenatal screening, routinely performing serologic tests for all women of childbearing age to determine susceptibility (so that vaccine is given only to proven susceptible women) can be effective but is expensive. Also, 2 visits to the health-care provider would be necessary — one for screening and one for vaccination. Accordingly, rubella vaccination of a woman who is not known to be pregnant and has no history of vaccination is justifiable without serologic testing — and may be preferable, particularly when costs of serology are high and follow-up of identified susceptible women for vaccination is not assured."{33} Postpubertal females should be informed of the frequent occurrence of generally self-limited arthralgia and/or arthritis beginning 2 to 4 weeks after vaccination (see ADVERSE REACTIONS). Postpartum Women It has been found convenient in many instances tovaccinate rubella-susceptible women in the immediate postpartum period (see PRECAUTIONS, Nursing Mothers). Other Populations Previously unvaccinated children older than 12 months who are in contact with susceptible pregnant women should receive live attenuated rubella vaccine (such as that contained in monovalent rubella vaccine or in M-M-R II) to reduce the risk of exposure of the pregnant woman. Individuals planning travel outside the United States, if not immune, can acquire measles, mumps, or rubella and import these diseases into the United States. Therefore, prior to international travel, individuals known to be susceptible to one or more ofthese diseases can either receive the indicated monovalent vaccine (measles, mumps, or rubella), or a combination vaccine as appropriate. However, M-M-R IIis preferred for persons likely to be susceptible to mumps and rubella; and if monovalent measles vaccine is not readily available, travelers should receive M-M-R IIregardless of their immune status to mumps or rubella.{34-36} Vaccination is recommended for susceptible individuals in high-risk groups such as college students, health-care workers, and military personnel.{33,34,37} According to ACIP recommendations, most persons born in 1956 or earlier are likely to have been infected with measles naturally and generally need not be considered susceptible. All children, adolescents, and adults born after 1956 are considered susceptible and should be vaccinated, if there are no contraindications. This includes persons who may be immune to measles but who lack adequate documentation of immunity suchas: (1) physician-diagnosed measles, (2) laboratory evidence of measles immunity, or (3) adequate immunization with live measles vaccine on or after the first birthday.{34}The ACIP recommends that "Persons vaccinated with inactivated vaccine followed within 3 months by live vaccine should be revaccinated with two doses of live vaccine. Revaccination is particularly important when the risk of exposure to wild-type measles virus is increased, as may occur during international travel."{34} Post-Exposure Vaccination Vaccination of individuals exposed to wild-type measles may provide some protection if the vaccine can be administered within 72 hours of exposure.If, however, vaccine is given a few days before exposure, substantial protection may be afforded.{34,38,39} There isno conclusive evidence that vaccination of individuals recently exposed to wild-type mumps or wild-type rubella will provide protection.{33,37} Use With Other Vaccines See DOSAGE AND ADMINISTRATION, Use With Other Vaccines. CONTRAINDICATIONS Hypersensitivity to any component ofthe vaccine, including gelatin.{40} Do not give M-M-R IIto pregnant females; the possible effects of the vaccine on fetal development are unknown at this time. If vaccination of postpubertal females is undertaken, pregnancy should be avoided for three months following vaccination (see INDICATIONS AND USAGE, Non-Pregnant Adolescent and Adult Females and PRECAUTIONS, Pregnancy). 4 Anaphylactic or anaphylactoid reactions to neomycin(each dose of reconstituted vaccine contains approximately 25 mcg of neomycin). Febrile respiratory illness or other active febrile infection. However, the ACIP has recommended that all vaccines can be administered to persons with minorillnesses such as diarrhea, mild upper respiratory infection with or without low-grade fever,or other low-grade febrile illness.{41} Patients receiving immunosuppressive therapy. Thiscontraindication does not apply to patients who are receiving corticosteroids as replacement therapy, e.g., for Addison's disease. Individuals with blood dyscrasias, leukemia, lymphomas of any type, or other malignant neoplasms affecting the bone marrow orlymphatic systems. Primary and acquired immunodeficiency states, including patients who are immunosuppressed in association with AIDS or other clinical manifestations of infection with human immunodeficiency viruses;{41-43}cellular immune deficiencies; and hypogammaglobulinemic and dysgammaglobulinemic states. Measles inclusion body encephalitis{44}(MIBE), pneumonitis{45} and death as a direct consequence of disseminated measles vaccine virus infection have been reported in immunocompromised individuals inadvertently vaccinated with measles-containing vaccine. Individuals with a family history of congenital or hereditary immunodeficiency, until the immune competence of the potential vaccine recipient is demonstrated. WARNINGS Due caution should be employed in administration of M-M-R IIto persons with a history of cerebral injury, individual or family histories of convulsions, or any other condition in which stress due to fever should be avoided. The physician should be alert to the temperature elevation which may occur following vaccination (see ADVERSE REACTIONS). Hypersensitivity to Eggs Live measles vaccine and live mumps vaccine are produced in chick embryo cell culture. Persons with a history of anaphylactic, anaphylactoid,or other immediate reactions (e.g., hives, swelling of the mouth and throat, difficulty breathing, hypotension, orshock) subsequent to egg ingestion may be at an enhanced risk of immediate-type hypersensitivity reactions after receiving vaccines containing traces of chick embryo antigen. The potential risk to benefit ratio should be carefully evaluated before considering vaccination in such cases. Such individuals may be vaccinated with extreme caution, having adequate treatment on hand should a reaction occur (see PRECAUTIONS).{46} However, the AAP has stated, "Most children with a history of anaphylactic reactions to eggs have no untoward reactions to measles or MMR vaccine. Persons are not at increased risk if they have egg allergies that are not anaphylactic, and they should be vaccinated in the usual manner. In addition, skin testing of egg-allergic children with vaccine hasnot been predictive of which children will have an immediate hypersensitivity reaction...Persons with allergies to chickens or chicken feathers are not at increased risk of reaction to the vaccine."{47}Hypersensitivity to Neomycin The AAP states, "Persons who have experienced anaphylactic reactions to topically or systemically administered neomycin should not receive measles vaccine. Most often, however, neomycin allergy manifests as a contact dermatitis, which is a delayed-type (cell-mediated) immune response rather than anaphylaxis. In such persons, an adverse reaction toneomycin in the vaccine would be an erythematous, pruritic nodule or papule, 48 to 96 hours after vaccination.A history of contact dermatitis to neomycin is not a contraindication to receiving measles vaccine."{47} Thrombocytopenia Individuals with current thrombocytopenia may develop more severe thrombocytopenia following vaccination. In addition, individuals who experienced thrombocytopenia with the first dose of M-M-R II(or its component vaccines) may develop thrombocytopenia with repeat doses. Serologic status may be evaluated to determine whether or not additional doses of vaccine are needed. The potential risk to benefit ratio should be carefully evaluated before considering vaccination in such cases (see ADVERSE REACTIONS). 5 PRECAUTIONS General Adequate treatment provisions, including epinephrine injection (1:1000), should be available for immediate use should an anaphylactic or anaphylactoid reaction occur. Special care should be taken to ensure that the injection does not enter a blood vessel. Children and young adults who are known to be infected with human immunodeficiency viruses and are not immunosuppressed may be vaccinated. However,vaccinees who are infected with HIV should be monitored closely for vaccine-preventable diseases because immunization may be less effective than for uninfected persons (see CONTRAINDICATIONS).{42,43} Vaccination should be deferred for 3 months or longer following blood or plasma transfusions, or administration of immune globulin (human).{47} Excretion of small amounts of the live attenuated rubella virus from the nose or throat has occurred in the majority of susceptible individuals 7 to 28 days after vaccination. There is no confirmed evidence to indicate that such virus is transmitted to susceptible persons who are in contact with the vaccinated individuals. Consequently, transmission through close personal contact, while accepted as a theoretical possibility, is not regarded as a significant risk.{33} However, transmission of the rubella vaccine virus to infants via breast milk has been documented (see Nursing Mothers). There are no reports of transmission of live attenuated measles or mumps viruses from vaccinees to susceptible contacts. It has been reported that live attenuated measles, mumps and rubella virus vaccines given individually may result in a temporary depression of tuberculin skin sensitivity. Therefore, if a tuberculin test is to be done, it should be administered either before or simultaneously with M-M-R II. Children under treatment for tuberculosis have notexperienced exacerbation of the disease when immunized with live measles virus vaccine;{48} no studies have been reported to date of the effect of measles virus vaccines on untreated tuberculous children. However, individuals with active untreated tuberculosis should not be vaccinated. As for any vaccine, vaccination with M-M-R IImay not result in protection in 100% of vaccinees. The health-care provider should determine the currenthealth status and previous vaccination history of the vaccinee. The health-care provider should question the patient, parent, or guardian about reactions to a previous dose of M-M-R IIor other measles-, mumps-, or rubella-containing vaccines. Information for Patients The health-care provider should provide the vaccine information required to be given with each vaccination to the patient, parent, or guardian. The health-care provider should inform the patient, parent, or guardian of the benefits and risks associated with vaccination. For risks associated with vaccination see WARNINGS, PRECAUTIONS, and ADVERSE REACTIONS. Patients, parents, or guardians should be instructed toreport any serious adverse reactions to their health-care provider who in turn should report such events to the U.S. Department of Health and Human Services through the Vaccine Adverse Event Reporting System (VAERS), 1-800-822-7967.{49} Pregnancy should be avoided for 3 months following vaccination, and patients should be informed of the reasons for this precaution (see INDICATIONS AND USAGE, Non-Pregnant Adolescent and Adult Females, CONTRAINDICATIONS, and PRECAUTIONS, Pregnancy). Laboratory Tests See INDICATIONS AND USAGE, Non-Pregnant Adolescent and Adult Females, for Rubella Susceptibility Testing, and CLINICAL PHARMACOLOGY. Drug Interactions See DOSAGE AND ADMINISTRATION, Use With Other Vaccines. Immunosuppressive Therapy The immune status of patients about to undergo immunosuppressive therapy should be evaluated so that the physician can consider whether vaccination prior to the initiation of treatment is indicated (see CONTRAINDICATIONS and PRECAUTIONS). The ACIP has stated that "patients with leukemia in remission who have not received chemotherapy for at least 3 months may receive live virus vaccines. Short-term (<2 weeks), low- to moderate-dose systemic corticosteroid therapy, topical steroid therapy (e.g. nasal, skin), long-term alternate-day 6 treatment with low to moderate doses of short-acting systemic steroid, and intra-articular, bursal, or tendon injection of corticosteroids are not immunosuppressive in their usual doses and do not contraindicate the administration of [measles, mumps, or rubella vaccine]."{33,34,37} Immune Globulin Administration of immune globulins concurrently with M-M-R IImay interfere with the expected immune response.{33,34,47} See also PRECAUTIONS, General. Carcinogenesis, Mutagenesis, Impairment of Fertility M-M-R IIhas not been evaluated for carcinogenic or mutagenic potential, or potential to impair fertility. Pregnancy Pregnancy Category C Animal reproduction studies have not been conducted with M-M-R II. It is also not known whether M-M-R IIcan cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Therefore, the vaccine should not be administered to pregnant females; furthermore, pregnancy should be avoided for 3 months following vaccination (see INDICATIONS AND USAGE, Non-Pregnant Adolescent and Adult Femalesand CONTRAINDICATIONS). In counseling women who are inadvertentlyvaccinated when pregnant or who become pregnant within 3 months of vaccination, the physician should be aware of the following: (1) In a 10-year survey involving over 700 pregnant women who received rubella vaccine within 3 months before or after conception (of whom 189 received the Wistar RA 27/3 strain), none of the newborns had abnormalities compatible with congenital rubella syndrome;{50} (2) Mumps infection during the first trimester of pregnancy may increase the rate of spontaneous abortion. Although mumps vaccine virus has been shown to infect the placenta and fetus, there is no evidence that it causes congenital malformations in humans;{37} and (3) Reports have indicated that contracting wild-type measles during pregnancy enhances fetal risk. Increased rates of spontaneous abortion, stillbirth, congenital defects and prematurity have been observed subsequent to infection with wild-type measles during pregnancy.{51,52} There are no adequate studies of the attenuated (vaccine) strain of measles virus in pregnancy. However, it would be prudent to assume that the vaccine strain of virus is also capable of inducing adverse fetal effects. Nursing Mothers It is not known whether measles or mumps vaccine virus is secreted in human milk. Recent studies have shown that lactating postpartum women immunized with live attenuated rubella vaccine may secrete the virus in breast milk and transmit itto breast-fed infants.{53} In the infants with serological evidence of rubella infection, none exhibited severe disease; however, one exhibited mild clinical illness typical of acquired rubella.{54,55} Caution should be exercised when M-M-R IIis administered to a nursing woman. Pediatric Use Safety and effectiveness of measles vaccine in infants below the age of6 months have not been established (see also CLINICAL PHARMACOLOGY).Safety and effectiveness of mumps and rubella vaccine in infants less than 12 monthsof age have not been established. Geriatric Use Clinical studies of M-M-R IIdid not include sufficient numbers of seronegative subjects aged 65 and over to determine whether they respond differentlyfrom younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger subjects. ADVERSE REACTIONS The following adverse reactions are listed in decreasing order of severity, without regard to causality, within each body system category and have been reported during clinical trials, with use of the marketed vaccine, or with use of monovalent or bivalentvaccine containing measles, mumps, or rubella: Body as a Whole Panniculitis; atypical measles; fever; syncope; headache; dizziness; malaise; irritability. Cardiovascular System Vasculitis. Digestive System Pancreatitis; diarrhea; vomiting; parotitis; nausea.

Nervous System: Encephalitis; encephalopathy; measles inclusion body encephalitis (MIBE) (see CONTRAINDICATIONS); subacute sclerosing panencephalitis (SSPE); Guillain-Barré Syndrome (GBS); acute disseminated encephalomyelitis (ADEM); transverse myelitis; febrile convulsions; afebrile convulsions or seizures; ataxia; polyneuritis; polyneuropathy; ocular palsies; paresthesia. aseptic meningitis

Adverse Reactions To The MMR or MMRV From Vaccine Insert

Respiratory System: Pneumonia; pneumonitis (see CONTRAINDICATIONS); sore throat; cough; rhinitis. Skin: Stevens-Johnson syndrome; erythema multiforme; urticaria; rash; measles-like rash;pruritis.Local reactions: including burning/stinging at injection site; wheal and flare; redness (erythema); swelling; induration; tenderness; vesiculation at injection site. Special Senses — Ear: Nerve deafness; otitis media. Eye: Retinitis; optic neuritis; papillitis; retrobulbar neuritis; conjunctivitis. Urogenital System: Epididymitis; orchitis.

http://www.merck.com/product/usa/pi_circulars/m/mmr_ii/mmr_ii_pi.pdf Other: Death

Dear Ms. Zacholski:We have approved your request to supplement your biologics license application for Measles, Mumps, and Rubella Virus Vaccine Live (MMR-II®) manufactured in your West Point, PA facility, to add the term “transverse myelitis” to the Adverse Reactions section of the package insert and to update the patient package insert to add the term "difficulty walking," based on post-marketing adverse event reports.http://www.fda.gov/biologicsbloodvaccines/vaccines/approvedproducts/ucm426312.htm

The scream is because of the child’s inflammation of the brain caused by the vaccine which will lead to neurological damage

We are a large experiment with adverse reactions being added after the vaccine is deemed to be safe & released to the public (Inadequate safety testing)

MMRV (ProQuad) IngredientsBovine (cow, specifically aborted calf) Albumin or Serum, Gelatin, Human Serum Albumin, Monosodium L-glutamate, Neomycin, Sodium Phosphate Dibasic, Sodium Bicarbonate, Sorbitol, Sucrose, Potassium Phosphate Monobasic, Potassium Chloride, Potassium Phosphate Dibasic, MRC-5 Cellular Protein- Aborted male Lung tissue obtained September 1966

https://www.facebook.com/photo.php?fbid=10152740935448170&set=p.10152740935448170&type=1&theater

• Mass use of Penicillin started in 1944 in the U.S. and had little to do with decrease in Diphtheria or Pertussis mortality rates

• All diseases had a similar downward trend in the U.S. before vaccination United States mortality rates from various infectious diseases from 1900 to 1965. (Vital Statistics of the United States 1937, 1938, 1943, 1944, 1949, 1960, 1967, 1976, 1987, 1992; Historical Statistics of the United States— Colonial Times to 1970 Part 1; Health, United States, 2004, US Department of Health and Human Services; Vital Records & Health Data Development Section, Michigan Department of Community Health; US Census Bureau, Statistical Abstract of the United States: 2003; Reported Cases and Deaths from Vaccine Preventable Diseases, United States, 1950–2008)

http://www.dissolvingillusions.com/wp-content/uploads/2013/03/G14.3-US-Deaths-1900-1965.png

http://www.dissolvingillusions.com/wp-content/uploads/2013/03/G11.2-UK-Deaths-1838-1978.png

• No Vaccine for Scarlet Fever and Scarlet fever had the same downward trend as the other diseases• Creation of Sanitation, Clean Drinking water, better Nutrition and Personal Hygiene Including

hand Washing are the reasons why Disease declined and lack of these factors is the reason why disease still persist in third world Countries

• The more stringent the vaccination for smallpox the more outbreaks of smallpoxEngland and Wales mortality rates from various infectious diseases from 1838 to 1978. (Record of mortality in England and Wales for 95 years as provided by the Office of National Statistics, published 1997).

The Government, the schools will send home unvaccinated children during an outbreak while the shedding vaccinated children who are causing the outbreaks are allowed to stay in school

http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM123789.pdf

Every vaccine insert states that this vaccine has not been tested for carcinogenesis, Mutagenesis and Impairment of Infertility. We know there are 4 known carcinogens in nearly all vaccines.

http://www.hopkinsmedicine.org/kimmel_cancer_center/patient_information/Patient%20Guide%20Final.pdf

• More confirmation of Live virus shedding, causing disease. Page 113 of 136. All of a sudden, after 10 years it was changed on 3-2015 to hide the fact that the vaccinated shed and spread disease

• Influenza and Pneumonia accounting for over 100 deaths every year between the two of them.

• DTP, than Polio and Haemophilus is associated with many deaths

http://www.medalerts.org/analysis/archives/628

The Federal Register is a daily publication of the US federal government that issues proposed and final administrative regulations of federal agencies. https://www.federalregister.gov/

The above policy about ignoring all safety matters with regards to vaccination was adopted so that the goals of the Government and Pharmaceuticals to force vaccinate every human on earth could go forward in order to profit from causing autoimmune disease, allergies, asthma, cancer and many other chronic illness with death as an unintended consequence. This specific quote was in regard to the Polio vaccine which was the first large campaign to convince the public that vaccines were a needed for health.

Google (Federal register/ vol. 49/ No.107/Friday, June 1, 1984/ Rules and Regulations) for the PDF

http://www.hhs.gov/nvpo/nvac/meetings/pastmeetings/2014/mulach_global_vaccine_feb2014nvac.pdf

THE PLAN TO FORCE VACCINATE EVERYONE ON THIS PLANET BY 2020 AT THE EXPENSE OF OUR HEALTH AND LIFE FOR GOV’T, PHARMACEUTICAL AND MEDICAL PROFIT The Decade of Vaccines Global Vaccine Action Plan:Global Vaccine & Immunization Research Forum

What does Bill Gates have to say about using vaccines to reduce population (Eugenics) https://www.youtube.com/watch?v=8BobKXkrt8M andDr. Russell Blaylock, Neurosurgeon and researcher on fluoride and vaccines for Eugenics https://www.youtube.com/watch?v=A3LUD53q_Pg

Recommended Videos to learn the facts of vaccinationMy 150 slide Power Point that reads like a book “Exposing the Myth of Vaccination, Essential Information You Need to Know to be Fully Informed” Explore recommended websites and videos starting on slide 132

http://www.slideshare.net/db61/exposing-the-myth-of-vaccination-essential-information-you-need-to-know-to-be-fully-informed-30978670

Do vaccines cause autism? Highly informative video narrated by Rob Schneider explaining the Vaccine Injury Court

https://www.youtube.com/watch?v=xv_IaLHwgAQ

Silent Epidemic; The Untold Story of Vaccines - Movie - directed by Gary Null

https://www.youtube.com/watch?v=lJGyN3gCsBg

How Vaccines Harm Child Brain Development - Dr Russell Blaylock MD

https://www.youtube.com/watch?v=7QBcMYqlaDs

Lethal Injection: The Story of Vaccination

https://www.youtube.com/watch?v=jdkWZgFPia0

Vaccine Nation - FULL LENGTH

https://www.youtube.com/watch?v=j8nrdybZZzA

Audio & Videos by Dr. Suzanne Humphries, MD, Nephrologist and vaccine researcher and historianMUST LISTEN TO Radio Interview with Dr. Suzanne Humphries on Polio, the science and many dangers of Vaccines “Honesty vs. Policy”https://kpfa.org/player/?audio=184162

Vaccines-Honesty vs Policy - Part I. Is Dr. Humphries a quack homeopath? (View all 6 Parts) How Dr. Suzanne Humphries after 19 years of believing in vaccines started connecting the dots, questioning vaccines, her real life experience, the research that led her to investigate more which eventually led her to vehemently oppose vaccines

https://www.youtube.com/watch?v=cLrqmvjrIjI

Dr. Suzanne Humphries - Neonatal Immunity: The First Three Years Pt 1 (View all 4 Parts)

https://www.youtube.com/watch?v=wL8srdLw4c0

Dr. Suzanne Humphries. Aluminum is toxic to all life forms: The case against aluminum in vaccines.

https://www.youtube.com/watch?v=LZe99K12740

Dr. Suzanne Humphries Lecture on vaccines and health FULL PART ONE (View all 4 parts)

https://www.youtube.com/watch?v=SFQQOv-Oi6U

Lecture on vitamin C by brilliant Suzanne Humphries. High dosage Vitamin C has been proven by Dr. Frederick R. Klenner M.D. to cure almost any infectious diseases including curing 60 out of 60 cases of Polio within 3 days in 1948 with IV vitamin C and was suppressed by the pharmaceuticals and medical establishment

https://www.youtube.com/watch?v=y0LLX0sgwAU

Recommended DVD’s & Books to PurchaseDr. Thomas Levy, Cardiologist, Attorney and an expert on Vitamin C. Author of several eye opening books on using vitamin C to reverse and prevent atherosclerosis and to cure just about any infectious disease including Polio as proven by Dr. Frederick Klenner in 1948 when he cured 60 out of 60 Polio cases within three days with High dosage IV Vitamin C. Be sure to purchase a book so that you can receive a FREE DVD set “Vitamin C, the facts, the fiction and the law”. And New Zealand 60 minutes program on a man left for dead by conventional medicine and high dosage vitamin C brought him back to life “ Living Proof”

http://www.peakenergy.com/

Book by Dr. Suzanne Humphries “Dissolving Illusions, Disease, Vaccines and the Forgotten History

http://www.dissolvingillusions.com/

Dr. Sherrie Tenpenny, DO and certified emergency room doctor who ran an ER for 12 years and has examined and researched vaccines more than anyone. Has great videos and books to learn from

https://www.youtube.com/results?search_query=dr+sherri+tenpenny+videos+on+vaccines

Visit Dr. Sherri Tenpenny’s web site for vaccine information, over 6,500 peer reviewed research articles on the dangers of vaccines and growing, videos, books sign up for news letter.

http://drtenpenny.com/#

My 150 slide Power Point that reads like a book “Exposing the Myth of Vaccination, Essential Information You Need to Know to be Fully Informed”. Explore recommended websites and videos starting on slide 132

http://www.slideshare.net/db61/exposing-the-myth-of-vaccination-essential-information-you-need-to-know-to-be-fully-informed-30978670