Vaccine News – How the Government is Hiding Vaccine-Related Deaths

Riassunto del flash mob di stamani al Senato della Repubblica…pochi ma BBONI!!! Grazie alle forze dell’ordine che sno state stupende!!!!
Summary of this morning’s flash mob in the Senate of the republic… a few but bboni!!! Thanks to the forces of order that sno were!!!!

You”ll be amazed how even the most trivial vaccine science is argued over by pro-vaccine doctors!
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Talk Host Attacks #Vaccine Science using Army Men!?! #HighWire #OhSnap @HighWireTalk @HighWireRadio

A nombre de AFECTADAS MEXICO VACUNA PAPILOMA HUMANO
Agradecemos a RADIO FORMULA PROYECTO PUENTE a su Titular
LUIS ALBERTO MEDINA
Datos para comprender la ENTREVISTA ya que por los tiempos no se puede extender en explicaciones.
HOSPITAL GENERAL REGIONAL N1 INSTITUTO MEXICANO DEL SEGURO SOCIAL IMSS SONORA.
HOSPITAL PEDIÁTRICO CENTRO MÉDICO NACIONAL DE OCCIDENTE IMSS JALISCO, MÉXICO
FICHA TÉCNICA . Es el documento autorizado donde se reflejan las condiciones de uso autorizadas para el medicamento y recoge la información científica esencial para los médicos y otros profesionales sanitarios. Aporta la información necesaria para su aplicación terapéutica: indicaciones (en que enfermedad/enfermedades y circunstancias está demostrada su eficacia y seguridad), posología, precauciones, contraindicaciones, reacciones adversas, uso en condiciones especiales (niños, embarazo, lactancia,..) y también resume los datos clínicos, propiedades farmacológicas o datos preclínicos sobre seguridad, que ayudan al medico a saber en qué tipo de pacientes puede o no utilizarlo y le guia sobre como puede comportarse el farmaco.
En el caso de la Vacuna VPH su ficha técnica es un libro de 100 páginas donde se especifica un listado grande de reacciones adversas como respuestas autoinmunes, daño neurológico, desmayos, etc.
SOMATIZACIÓN. Es un diagnóstico psiquiátrico aplicado a pacientes quienes se quejan crónica y persistentemente de varios síntomas físicos que no tienen un origen físico identificable.
ES EL DIAGNÓSTICO MÁS COMÚN QUE SE LES ESTA DANDO A LAS NIÑAS QUE PRESENTAN REACCIÓN ADVERSA, PERDIENDO TIEMPO EN VALORACIÓN OPORTUNA Y TRATAMIENTO. Negando nexo causal post vacunal.
PARESTESIA. Se define como la sensación anormal de los sentidos o de la sensibilidad general que se traduce por una sensación de hormigueo, adormecimiento, acorchamiento, etc., producido por una patología en cualquier sector de las estructuras del sistema nervioso central o periférico1
El entumecimiento y hormigueo son sensaciones anormales que se pueden producir en cualquier parte del cuerpo, pero son más usuales en las manos, pies, brazos y piernas.
Los signos y síntomas característicos de la parestesia pueden ser permanentes o transitorios. Sin embargo, en la mayor parte de los casos, se trata de una patología temporal causada por la presencia de algún tipo de presión sobre los terminales nerviosos
LINK YOUTUBE PROYECTO PUENTE
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In the name of affected mexico human papilloma vaccine
We thank radio formula project bridge to its headline
Luis Alberto Medina
Data to understand the interview as the times cannot be extended to explanations.
Regional General Hospital N1 Mexican Social Insurance Institute Sonora.
Paediatric Hospital National Medical Center of West Imss Jalisco, Mexico
Technical Information. It is the authorized document where the conditions of use authorised for the medicinal product are reflected and contains the essential scientific information for doctors and other health professionals. Provides the information necessary for its therapeutic application: Indications (in which disease / diseases and circumstances is proven to be effective and safety), posology, precautions, contraindications, adverse reactions, use in special conditions (children, pregnancy, lactation,..) and It also summarizes clinical data, pharmacological properties or preclinical safety data, which help the doctor to know what type of patients may or may not use and guide him on how the drug can behave.
In the case of the HPV vaccine its technical sheet is a 100-page book specifying a large list of adverse reactions such as autoimmune responses, neurological damage, fainting, etc.
Somatization. It is a psychiatric diagnosis applied to patients who are chronically and persistently complaining of several physical symptoms that do not have an identifiable physical origin.
It is the most common diagnosis given to girls who have adverse reactions, wasting time in timely assessment and treatment. Denying Post-vaccination causal link.
Paraesthesia. It is defined as the abnormal sensation of the senses or general sensitivity resulting from a sensation of tingling, numbness, Acorchamiento, etc., produced by a pathology in any sector of the central nervous system or periférico1
Numbness and tingling are abnormal sensations that can occur in any part of the body, but are more commonly used in hands, feet, arms and legs.
Signs and symptoms characteristic of may be permanent or transient. However, in most cases, it is a temporary pathology caused by the presence of some kind of pressure on nervous terminals
Link Youtube project bridge
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https://www.youtube.com/watch?v=2ef_We6JOKs&t=322s

Toni Bark and her son Ayal join Del to talk about study drugs, “owning your immunity”, latent viral infections, and vaccines in the military. @HighWireTalk @DelBigtree @UBNRadioTV

100% Proof! Human DNA in Vaccines
Presentation recorded on February 16, 2017 in Sonora, California with Marcella Piper-Terry.
#Vaxxed #PrayBig #RecombinantDNA #InsertionalMutagenesis #FetalCellLine #ProLife #Abortion #ChooseLife #RespectLife #MarchForLife #MRC5 #WI38 #RA273 #WALVAX2
Youtube Link: https://youtu.be/dlqFQLLOTEU

The Vaccine Culture War is heating up. Ground zero is America, Europe and other economically developed countries, where the pharmaceutical industrial complex is raising an iron fist to protect multi-billion dollar profits by disempowering the people.
In America, professors and doctors in academia and government are profiling parents by class and race to shame and discredit those challenging vaccine orthodoxy. Elite members of the highest paid professions in our society are using academic journals and mainstream media to openly preach fear, hate, prejudice and discrimination against people who disagree with them about vaccination.
Please read the fully referenced commentary and leave your comments here >>> http://ow.ly/QcG930dMRN0

‘It’s just kids coming in for haircuts’ 💇
What’s it like for an autistic person to have a trim?

#VaXism NEWS

The Unseen Encyclopedia

Study – Mercury, lead, and zinc in baby teeth of children with autism versus controls.
Abstract
This study determined the level of mercury, lead, and zinc in baby teeth of children with autism spectrum disorder (n = 15, age 6.1 +/- 2.2 yr) and typically developing children (n = 11, age = 7 +/- 1.7 yr). Children with autism had significantly (2.1-fold) higher levels of mercury but similar levels of lead and similar levels of zinc. Children with autism also had significantly higher usage of oral antibiotics during their first 12 mo of life, and possibly higher usage of oral antibiotics during their first 36 mo of life. Baby teeth are a good measure of cumulative exposure to toxic metals during fetal development and early infancy, so this study suggests that children with autism had a higher body burden of mercury during fetal/infant development. Antibiotic use is known to almost completely inhibit excretion of mercury in rats due to alteration of gut flora. Thus, higher use of oral antibiotics in the children with autism may have reduced their ability to excrete mercury, and hence may partially explain the higher level in baby teeth. Higher usage of oral antibiotics in infancy may also partially explain the high incidence of chronic gastrointestinal problems in individuals with autism.

New Concerns about the Human Papillomavirus Vaccine
American College of Pediatricians – January 2016
The American College of Pediatricians (The College) is committed to the health and well-being of children, including prevention of disease by vaccines. It has recently come to the attention of the College that one of the recommended vaccines could possibly be associated with the very rare but serious condition of premature ovarian failure (POF), also known as premature menopause. There have been two case report series (3 cases each) published since 2013 in which post-menarcheal adolescent girls developed laboratory documented POF within weeks to several years of receiving Gardasil, a four-strain human papillomavirus vaccine (HPV4).1,2 Adverse events that occur after vaccines are frequently not caused by the vaccine and there has not been a noticeable rise in POF cases in the last 9 years since HPV4 vaccine has been widely used.
Nevertheless there are legitimate concerns that should be addressed: (1) long-term ovarian function was not assessed in either the original rat safety studies3,4 or in the human vaccine trials, (2) most primary care physicians are probably unaware of a possible association between HPV4 and POF and may not consider reporting POF cases or prolonged amenorrhea (missing menstrual periods) to the Vaccine Adverse Event Reporting System (VAERS), (3) potential mechanisms of action have been postulated based on autoimmune associations with the aluminum adjuvant used1 and previously documented ovarian toxicity in rats from another component, polysorbate 80,2 and (4) since licensure of Gardasil® in 2006, there have been about 213 VAERS reports (per the publicly available CDC WONDER VAERS database) involving amenorrhea, POF or premature menopause, 88% of which have been associated with Gardasil®.5 The two-strain HPV2, CervarixTM, was licensed late in 2009 and accounts for 4.7 % of VAERS amenorrhea reports since 2006, and 8.5% of those reports from February 2010 through May 2015. This compares to the pre-HPV vaccine period from 1990 to 2006 during which no cases of POF or premature menopause and 32 cases of amenorrhea were reported to VAERS.

HPV Vaccine: American College of Pediatricians Issues Rare Warning Against Vaccine Due to Premature Ovarian Failure
By: Tara West
In an unprecedented move, the American College of Pediatricians has issued a warning against a vaccine that has been approved by the FDA and CDC. The College says that they are committed to the health and well-being of children, and due to their commitment to children’s health, they feel that safety concerns regarding the Human Papillomavirus Vaccine Gardasil should be made public.
The College says that in addition to concerning correlations between Gardasil and Premature Ovarian Failure, they are also concerned with the pre-release vaccine testing methods utilized by Gardasil maker Merck. Pre-licensure safety trials for Gardasil used a placebo that contained polysorbate 80 as well as an aluminum adjuvant, which are both contained within the vaccine. Therefore, if either of these ingredients could cause ovarian dysfunction, an increase in amenorrhea probably would not have been detected. The College notes that the placebo-controlled trials were highly questionable due to the fact that the placebos were actually not placebos at all.

Kickbacks: What Your Pediatrician Gets for Vaccinating
(And a Peek At what Big Pharma Gets)
The Role Insurance Companies Play and The Kickbacks Doctors Get
Vaccines are a Trillion Dollar Business and there are incentives at every corner for anyone playing a role in injecting them into the world’s population. Just take a look at what a doctor gets from Blue Cross Blue Shield.
(All of the information in the graphic and more can be found here, in the Blue Cross Blue Shield’s Physician’s Performance Recognition Program/Provider Incentive ProgramBlue Cross Blue Shield’s Physician’s Performance Recognition Program/Provider Incentive Program.)
http://www.whale.to/c/2016-BCN-BCBSM-Incentive-Program-Booklet.pdf

Now look at the schedule for vaccines.
In the United States in the 1950’s, children received 13 doses of four vaccines by age two. In the mid 1980’s, children received 15 doses of seven vaccines by age two. In 2010, the CDC recommended 37 doses of 14 vaccines by age two (Mercola and CDC). Now, in August of 2016, it is recommended that children receive 49 doses of 14 vaccines by age six, and 70 doses of 15 vaccines by age 18. These numbers just changed by 2 doses, as this month the CDC just announced that children going into 7th and 12th grades are now required to get the meningococcal vaccine – that’s 2 more does of vaccines making it 71 doses of vaccines by age 18 and adding close to sixty billion dollars into the pockets of big pharma.
The even scarier part – as of 2013, there were/are nearly 300 vaccines in development, as is proudly boasted in Pharma.com. Multiply 300 by thirty billion – that’s 9 TRILLION dollars in vaccines coming our way.
CDC Vaccine Price List
Just how much do vaccines cost the people giving them? Here’s a whole list from the CDC.
https://www.cdc.gov/vaccines/programs/vfc/awardees/vaccine-management/price-list/
For Information and Resources on Vaccines see:
Vaccines 101http://raisingnaturalkids.com/vaccine-info/
The most important message I want to relay about getting your children vaccinated: Do your research before deciding that you are going to vaccinate! Every parent wants what is best for his/her children, so doesn’t it make sense to take the time to actually get some background information and facts about vaccines before injecting them into a newborn baby? In my eyes we owe it to our children to look into anything they are exposed to, whether ingested, inhaled or injected, as children are dependent on parents to make the educated choices for them when they cannot do it themselves. If after having thoroughly researched both sides of the pros and cons of vaccinations and you decided to move forward with vaccinating your children, then that is a decision you are making based on knowledge, rather than blindly going into vaccinating just because it is what the government, and thus, the American Medical Association say (yes, I realize these are two major giants that people want to trust no matter what, but they are made up of individuals who don’t always have the good of the people in mind (or they are blinded to the truth as hidden by the CDC), as you will come to see in your research if you dig deep enough).
Being that I am not a medical expert, but a mother who does a lot of research to make sure I do the best for my kids, I will direct you to valuable links, books, documentaries and information about vaccinations, along with providing you with some of what I have learned along the way.
Interesting Facts
If you are just delving into your research, it is important to note there is a reason that the United States government actually has a Vaccine Injury Compensation Program, where they will “award” a set dollar amount in certain circumstances if a person is injured or dies due to a vaccine. This program protects the pharmaceutical companies in that a person cannot sue the companies that make the vaccinations (the money paid out comes from the taxpayers’ pockets)! This isn’t the case in other countries. For instance, this past February 2014, five French families have joined forces to take GlaxoSmithKline, Pfizer and Sanofi to court after their children were severely injured due to vaccines.

VACCINATIONS: PART I – MEDICAL RESEARCH ON SIDS AND EPIDEMICS
by: Scheibner, Viera, Ph.D.
Viera Scheibner is a retired principal research scientist with a doctorate in natural sciences. During her distinguished career, she has published three books and 90 scientific papers in prestigious scientific journals. Since the mid-80’s, she has done extensive research into vaccines and vaccinations. Her first research was in the area of Sudden Infant Death Syndrome (SIDS). She wasn’t even studying vaccinations, but she stumbled onto a relationship between SIDS and vaccinations that lead to a very deep study into vaccination literature in medical journals. In 1983, she published her book on the results of her research Vaccination: The Medical Assault on the Immune System. She often provides expert reports for court cases involving immunizations and vaccine-damaged individuals throughout the world.
SUDDEN INFANT DEATH SYNDROME (SIDS)
In 1985, I was introduced into the world of vaccinations through a breathing monitor invented by my husband, Leif Karlsson, who was a bio-medical engineer specializing in patient monitoring systems. Leif developed a computerized breathing monitor for babies which we called “Cotwatch”, short for ‘watching the cot’. Our monitor gives computer print-outs, and you can monitor for weeks on end, because Cotwatch is a non-touch medical technology. The sensor pad goes under the mattress; nothing is attached to the baby and the baby can roll all over the cot while the breathing is monitored. In 1986, pediatric researchers studying Crib Death Syndrome or Sudden Infant Death Syndrome (SIDS) believed babies were dying because of an inborn fault in the breathing control center in the brain. So they concentrated their studies on breathing. Many parents opted for monitoring their newborn babies’ breathing at home, and we collected feedback from all parents who used our monitor in this research.
OUR FIRST CASE HISTORY This baby was put on our monitor before he was vaccinated, and for more than three weeks, there were hardly any alarms at all. Then suddenly, the mother recorded a whole series of alarms. We thought there was a defect in the monitor, and I sent a different unit, but the alarms continued. After one night when they had six alarms in 24 hours their pediatrician advised them to stop monitoring. But if you have alarms on certain days and no alarms on other days, it is not the equipment malfunctioning; there is good reason for alarms like that. I transferred the baby’s forms onto a graph, but did not understand it at the time. Five years later, I telephoned the mother and asked her when the child was vaccinated. The first injection was given one day before these alarms started. The child hadn’t even recovered before the second injection was given. So there was a high level of stress caused by vaccines even when the child was not dying. There were no alarms before vaccination, and then a series of alarms. The alarms sound to tell you that your child is under stress when their breathing is shallow (hypopneas) or when their breathing ceases temporily (apneas).
We then informed the pediatric and SIDS researchers that the babies were having alarms after vaccinations. We were not critical of vaccines and we didn’t even know about the raging controversy surrounding vaccinations. At this point, the Crib Death Management Center pediatricians stopped sending parents to get our monitor. They didn’t want parents to know that vaccines were stressing their children. Until that time, I was actually pro-vaccination.
SIDS RESEARCH IGNORES THE STRESS ALARMS SIDS researchers call all the alarms which occur when the child is breathing very shallowly, but not dying, ‘false alarms’. Their notion of ‘false alarms’ actually prevents them from having any results. Instead of throwing these alarms into the garbage bin as false alarms we studied them, and did our own research using the computerized breathing monitor, recording the babies’ breathing longitudinally over weeks on end. Overnight six to eight hour studies are often used in SIDS research, but they are very misleading.

How the Government is Hiding Vaccine-Related Deaths
July 21, 2017 Comments by Brian Shilhavy
Editor, Health Impact News
This latest article by Robert F. Kennedy, Jr., explains how world governments go to great lengths to hide vaccine-related deaths.
The fact that vaccines do cause deaths sometimes is not even a fact in dispute. In addition to the deaths reported in the U.S. Vaccine Adverse Event Reporting System (VAERS), the Department of Justice supplies a quarterly report to the Advisory Commission on Childhood Vaccines on cases settled for vaccine injuries and deaths.
The American public is largely unaware that there is a “vaccine court” known as the National Vaccine Injury Compensation Program (NVICP). This program was started as a result of a law passed in 1986 that gave pharmaceutical companies total legal immunity from being sued due to injuries and deaths resulting from vaccines.
If you or a family member is injured or dies from vaccines, you must sue the federal government in this special vaccine court.
Many cases are litigated for years before a settlement is reached, and a November 2014 GAO report criticized the government for not making the public more aware that the National Vaccine Injury Compensation Program exists, and that there are funds available for vaccine injuries and deaths.
Therefore, the settlements represented by vaccine injuries and deaths included in the DOJ reports probably represent a small fraction of the actual vaccine injuries and deaths occurring in America today.
Also, as we have previously reported, the CDC lists 130 official ways for an infant to die, but vaccine deaths are not even an option. If the death does not fall into one of these 130 causes, it usually gets listed as SIDS (Sudden Infant Death Syndrome).
SIDS has skyrocketed since the 1986 National Vaccine Injury Compensation Program started.
Hiding Vaccine-Related Deaths With Semantic Sleight-of-Hand
By Robert F. Kennedy, Jr. – World Mercury Project
http://vaccineimpact.com/vaccine-injuries-and-deaths-compensated-through-vaccine-court/
https://www.hrsa.gov/advisorycommittees/childhoodvaccines/index.html

CDC Lists 131 Causes of Death For A Child but Omits Vaccines
More Vaccine Fatalities – Hidden in the Death Tables
“SIDS,” “suffocation in bed,” and death due to “unknown and unspecified causes,” are just three of the 130 official cause-of-death categories that might be concealing fatalities that were really caused by vaccination. Several other ICD categories are possible candidates for incorrect infant death classifications: unspecified viral diseases, diseases of the blood, diseases of the nervous system, unspecified diseases of the respiratory system, and shaken baby syndrome. All of these official categories may be repositories of vaccine-related infant deaths reclassified as common fatalities.
For example, a vaccine against rotavirus-induced diarrhea (Rotarix) was licensed by the Food and Drug Administration (FDA) in 2008. However, in a clinical study that evaluated the safety of this vaccine, vaccinated babies died at a significantly higher rate than non-vaccinated babies — mainly due to a statistical increase in pneumonia fatalities. (One biologically plausible explanation is that natural rotavirus infection might have a protective effect against respiratory infection.) Although these deaths appear to be vaccine related, coroners are likely to have misclassified them as pneumonia.
Some infant fatalities that occur shortly after vaccinations are incorrectly classified as shaken baby syndrome. Retinal and subdural bleeding can result from an adult that shook the baby or from vaccine damage. Expert testimony by medical practitioners has exonerated innocent parents of all charges against them. This is just another example of how the true cause of death can be reclassified or hidden within the death tables.
The practice of reclassifying ICD data greatly concerns the CDC “because inaccurate or inconsistent cause-of-death determination and reporting hamper the ability to monitor national trends, ascertain risk factors, and design and evaluate programs to prevent these deaths.” Thus, medical certification practices need to be monitored to determine how often vaccine-related infant deaths are being reclassified as ordinary mortality in the ICD. More importantly, parents need to be warned that vaccine safety is grossly overestimated when vaccine-related deaths are not being accurately documented.
Vaccine Safety, Informed Consent and Human Rights
There are 130 official ways for an infant to die (as categorized in the ICD), and one unofficial way for an infant to die: following an adverse reaction to one or more vaccines. When vaccine-related deaths are hidden within the death tables, parents are denied the ability to ascertain honest vaccine risk-to-benefit ratios, and true informed consent to vaccinations is not possible. When families are urged to vaccinate their children without access to accurate data on vaccine-related deaths, their human rights have been violated. Medical health authorities, pediatricians, and the vaccine industry then become criminal accomplices to each infant death caused by vaccines — even when vaccines are not officially acknowledged as the cause of death. Finding ways to increase vaccine safety, providing families with true informed consent, and preserving human rights must be the top priorities.

Study – Evidence that Food Proteins in Vaccines Cause the Development of Food Allergies and Its Implications for Vaccine Policy
Corresponding Author: Vinu Arumugham
San Jose, CA, USA
Abstract
Nobel Laureate Charles Richet demonstrated over a hundred years ago that injecting a protein into animals or humans causes immune system sensitization to that protein. Subsequent exposure to the protein can result in allergic reactions or anaphylaxis. This fact has since been demonstrated over and over again in humans and animal models. The Institute of Medicine (IOM) confirmed that food proteins in vaccines cause food allergy, in its 2011 report on vaccine adverse events. The IOM’s confirmation is the latest and most authoritative since Dr. Richet’s discovery. Many vaccines and injections contain food proteins. Many studies since 1940 have demonstrated that food proteins in vaccines cause sensitization in humans. Allergens in vaccines are not fully disclosed. No safe dosage level for injected allergens has been established. As a result, allergen quantities in vaccines and injections are not regulated. Allergen quantities in vaccine excipients are also not regulated. It has been demonstrated that a smaller quantity of allergen is needed to cause sensitization than elicitation. It is well recognized that many currently approved vaccines have enough allergen to cause anaphylaxis. Therefore, they contain more than enough allergen to cause sensitization. Children today have fewer childhood infectious diseases. They have less exposure to helminths. C-section birth rates have increased in the last few decades by 50%. C-section births are known to result in sub-optimal gut micro biome in the newborn. All the above result in an immune imbalance biased towards atopy. Vaccine schedules today include 30-40 shots. Up to five shots may be simultaneously administered in one sitting. Vaccines contain adjuvants such as pertussis toxins and aluminum compounds that also bias towards allergy. Adjuvants also increase the immunogenicity of injected food proteins. This combination of atopic children and food protein injection along with adjuvants, contributes to millions developing lifethreatening food allergies. Given the scale and severity of the food allergy epidemic, urgent action is needed to change vaccine policy concerning vaccine specifications, manufacture, vaccine package insert documentation requirements, the Vaccine Adverse Event Reporting System (VAERS) and the National Vaccine Injury compensation program. Many researchers have called for the removal of food proteins from vaccines and re-evaluation of adjuvants such as aluminum compounds. In the interim, food allergy warnings can be included in vaccine package inserts. Simultaneous administration of multiple vaccines can be stopped to avoid the combined negative effects of multiple food proteins and adjuvants.

 

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Vaccine News – Autism and the MMR Vaccine: The Most Diabolical Medical Scandal of the Century

Courts quietly confirm MMR Vaccine causes Autism
By Mark Wachtler
July 27, 2013. Austin. (ONN) After decades of passionate debate, parents probably missed the repeated admissions by drug companies and governments alike that vaccines do in fact cause autism. For concerned parents seeking the truth, it’s worth remembering that the exact same people who own the world’s drug companies also own America’s news outlets. Finding propaganda-free information has been difficult, until now.
Dr. Andrew Wakefield and family at a recent demonstration. Image courtesy of the Vaccine Resistance Movement.
At the center of the fifteen-year controversy is Dr. Andrew Wakefield of Austin, Texas. It was Dr. Wakefield that first publicized the link between stomach disorders and autism, and taking the findings one step further, the link between stomach disorders, autism and the Measles Mumps Rubella (MMR) vaccine.
For that discovery way back in 1996, and a subsequent research paper published by the doctor in 1998, Andrew Wakefield has found himself the victim of a world-wide smear campaign by drug corporations, governments and media companies. And while Dr. Wakefield has been persecuted and prosecuted to the extent of being unable to legally practice medicine because of his discovery, he has instead become a best-selling author, the founder of the Strategic Autism Initiative, and the Director of the Autism Media Channel.
But in recent months, courts, governments and vaccine manufacturers have quietly conceded the fact that the Measles Mumps Rubella (MMR) vaccine most likely does cause autism and stomach diseases. Pharmaceutical companies have even gone so far as to pay out massive monetary awards, totaling in the millions, to the victims in an attempt to compensate them for damages and to buy their silence.

Dr Wakefield: Govt. experts have conceded that MMR vaccine caused autism
This is the transcript of Dr. Andrew Wakefield’s response to the UK government blaming him for the current measles outbreak.
It was with that background and with that insight into the practices of the Joint Committee of Vaccination and Immunisation and I took the stand that I did on MMR. I was deeply and justifiably concerned. So the next question is beyond the fact that MMR vaccine is not safe and has not been adequately tested;  not just my opinion but the opinion of many; is does MMR vaccine cause autism.
Now this question has been answered not by me but by the courts, by the vaccine courts in Italy and in the United States of America where it appears that many children over the last 30 years have  been awarded millions of dollars for the fact that they have been brain-damaged by MMR vaccine and other vaccines and that brain-damage has led to autism. That is a fact.
Now it has been argued by the government that some poor judge has been forced into making this decision that on balance the vaccine cause the autism in the face and in contradiction to the evidence that is available, the scientific evidence. No. That is grossly misleading. Three of these cases the least; Poling, the Italian  case, and more recently the Mojabi case, were conceded by the government experts. In other words the government extrovert is,  the government themselves have conceded that the vaccine cause the autism. They didn’t fight the case. They conceded it based upon the evidence available to – all of it – that the MMR vaccine caused the child’s autism.
So this isn’t some poor judge being forced into a position in the absence of the evidence or in contradiction to the evidence. This is the government’s own experts conceding that the MMR vaccine caused the autism, or caused brain damage in this case that led to be autism. And what we have are millions of dollars being paid out to these children to fund their autism treatment so when the  government says it is not settled cases of autism, please bear in  mind that what they’re paying for the costs of the autism treatments. The government if it says that is speaking out of both sides of its mouth.

DTP Vaccine Increases Mortality in Young Infants 5 to 10-Fold Compared to Unvaccinated Infants
By Robert F. Kennedy, Jr.
For many years, public health advocates have vainly urged the CDC and WHO to conduct studies comparing vaccinated vs. unvaccinated populations to measure overall health outcomes.  Now a team of Scandinavian scientists has conducted such a study and the results are alarming.  That study, funded in part by the Danish government and lead by Dr. Soren Wengel Mogensen, was published in January in EBioMedicine.  Mogensen and his team of scientists found that African children inoculated with the DTP (diphtheria, tetanus and pertussis) vaccine, during the early 1980s had a 5-10 times greater mortality than their unvaccinated peers.
The data suggest that, while the vaccine protects against infection from those three bacteria, it makes children more susceptible to dying from other causes.
The scientists term the study a “natural experiment” since a birthday-based vaccination system employed for the Bandim Health Project (BHP) in Guinea Bissau, West Africa had the effect of creating a vaccinated cohort and a similarly situated unvaccinated control group.  In the time period covered by this study, Guinea-Bissau had 50% child mortality rates for children up to age 5.  Starting in 1978, BHP health care workers contacted pregnant mothers and encouraged them to visit infant weighing sessions provided by a BHP team every three months after their child’s birth.  Beginning in 1981, BHP offered vaccinations at the weighing sessions.  Since the DPT vaccine and OPV (oral polio) immunizations were offered only to children who were at least three months of age at the weighing sessions, the children’s random birthdays allowed for analysis of deaths between 3 and 5 months of age depending on vaccination status.  So, for example, a child born on January 1st and weighed on April 1st would be vaccinated, but a child born on February 1st would not be vaccinated until their following visit at age 5 months on July 1st.
In the primary analysis, DTP-vaccinated infants experienced mortalities five times greater than DTP-unvaccinated infants.  Mortalities to vaccinated girls were 9.98 times those among females in the unvaccinated control group, while mortalities to vaccinated boys were 3.93 times the controls.  Oddly, the scientists found that children receiving the oral polio vaccine simultaneously with DTP fared much better than children who did not.  The OPV vaccine appeared to modify the negative effect of the DTP vaccine, reducing mortalities to 3.52 times those experienced among the control group.  Overall, mortalities among vaccinated children were 10 times the control group when children received only the DTP.

Study – The Introduction of Diphtheria-Tetanus-Pertussis and Oral Polio Vaccine Among Young Infants in an Urban African Community: A Natural Experiment
Background:
We examined the introduction of diphtheria-tetanus-pertussis (DTP) and oral polio vaccine (OPV) in an urban community in Guinea-Bissau in the early 1980s.
Methods:
The child population hadbeen followed with 3-monthly nutritional weighingsessionssince 1978.From June 1981 DTP and OPV were offered from 3 months of age at these sessions. Due to the 3-monthly intervals between sessions, the children were allocated by birthday in a ‘natural experiment’ to receive vaccinations early or late between 3 and 5 months of age.We included children who were b 6 months of age when vaccinations started and children born until the end of December 1983. We compared mortality between 3 and 5 months of age of DTP-vaccinated and not-yet-DTP-vaccinated children in Cox proportional hazard models.
Results:
Among 3–5-month-old children, having received DTP (±OPV) was associated with a mortality hazard ratio (HR) of 5.00 (95% CI 1.53–16.3) comparedwith not-yet-DTP-vaccinated children. Differences inbackground factors did not explain the effect. The negative effect was particularly strong for children who had received DTP-only and no OPV (HR = 10.0 (2.61–38.6)). All-cause infant mortality after 3 months of age increased after the introduction of these vaccines (HR = 2.12 (1.07–4.19)).
Conclusion:
DTP was associated with increased mortality; OPV may modify the effect of DTP.
© 2017 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license

Govt. Still Pushing HPV Vaccine on Kids a Decade after JW Exposed Deadly Side Effects
MARCH 09, 2017
A decade after Judicial Watch exposed the dangers of a government-backed cervical cancer vaccine, a federal lawsuit highlights its perilous side effects including paralysis, seizures, nausea and death. Litigation was initiated by disgruntled parents because the government is still pushing the hazardous vaccine, manufactured by pharmaceutical giant Merck, on children as young as nine years old to treat a sexually transmitted disease.
The vaccine is called Gardasil and in the last ten years Judicial Watch has uncovered troves of government records documenting its harmful side effects. The vaccine was scandalously fast-tracked by the Food and Drug Administration (FDA) and was ardently promoted by the Obama administration as a miracle shot that can prevent certain strains of cervical cancer caused by Human Papillomavirus (HPV). Instead it’s been linked to thousands of debilitating side effects, according to the government’s own daunting statistics. This includes thousands of cases of paralysis, convulsions, blindness and dozens of deaths. Back in 2008, after receiving the first disturbing batch of records from the Centers for Disease Control and Prevention (CDC), Judicial Watch published a special report detailing Gardasil’s approval process, side effects, safety concerns and marketing practices. Undoubtedly, it illustrates a large-scale public health experiment.
Regardless, the government has continued promoting the vaccine while covering up its debilitating side effects, recommending it for girls—and more recently boys—starting at age 9. The Obama administration gave dozens of state and municipal health agencies tens of millions of dollars to boost the number of adolescents that get Gardasil. This includes targeting low-income and ethnic minority populations that receive “culturally sensitive” intervention in a variety of languages, including Spanish, Mandarin, Armenian and Korean. U.S. law forbids lawsuits against vaccine manufacturers, but Judicial Watch has obtained records from the Department of Health and Human Services (HHS) revealing that its National Vaccine Injury Compensation Program (VICP) has awarded nearly $6 million to dozens of victims in claims made against the very HPV vaccine it is pushing on children.
In 2014 a physician who worked at Merck denounced Gardasil as an ineffective vaccine with deadly side effects that serves no other purpose than to generate profit for its manufacturer. The former pharmaceutical industry doctor, Bernard Dalbergue, said Gardasil is useless, costs a fortune and that decision-makers at all levels are aware of it. “I predict that Gardasil will become the greatest medical scandal of all times because at some point in time, the evidence will add up to prove that this vaccine, technical and scientific feat that it may be, has absolutely no effect on cervical cancer and that all the very many adverse effects which destroy lives and even kill, serve no other purpose than to generate profit for the manufacturers,” Dr. Dalbergue said. He added that there is far too much financial interest for the vaccine to be withdrawn. Dr. Dalbergue’s statements were used by a member of the French Parliament as part of a broader campaign blasting Gardasil’s horrible safety record in Europe.

A Judicial Watch Special Report Examining the FDA’s HPV Vaccine Records
Detailing the Approval Process, Side-Effects, Safety Concerns and Marketing Practices of a Large-Scale Public Health Experiment
June 30, 2008
This Judicial Watch Special Report is an analysis of records obtained from the Food and Drug Administration (FDA) concerning a recent vaccine called Gardasil.  Gardasil helps protect against four types of human papillomavirus (HPV).  The vaccine was approved in May 2006 and was created and marketed by Merck & Company Incorporated.
The records include Merck’s patent and drug information submitted to the FDA, transcripts and briefing material from approval meetings, and reports documenting health, safety, and efficacy test results, as well as Vaccine Adverse Event Reporting System (VAERS) documents detailing 8,864 cases of adverse effects experienced by people after receiving the Gardasil vaccine.  VAERS reports show that at least eighteen people have died after receiving Gardasil.
Many health officials believe that adverse reactions to medications are widely underreported, therefore the actual number of adverse events occurring after vaccination with Gardasil is likely to be higher.  Judicial Watch obtained these records under the provisions of the Freedom of Information
Act (FOIA), 5 U.S.C. § 552.  The request, asking for documents concerning Gardasil, was originally submitted to the FDA on May 9, 2007.  The FDA produced documents on May 15, 2007; September 13, 2007; February 27, 2008, and June 10, 2008.
Judicial Watch uncovered thousands of pages of material pertaining to Gardasil, which is designed to prevent cervical cancer.  The controversial vaccine was fast-tracked for approval by the FDA despite concerns about Gardasil’s safety and long-term effects.  The vaccine is still in the testing stages (final report due September 30, 2009), but it is already being administered to thousands of young girls and women.
Mandatory vaccination has been opposed by the American College of Pediatrics and The New England Journal of Medicine.
Legislators in 41 states and Washington, DC have introduced legislation to require, fund or educate the public about the HPV vaccine and 17 states have enacted legislation.  Michigan, Texas and Virginia took steps toward mandatory vaccination for sixth grade girls; however, all three states have postponed that required mandate.
Judicial Watch is concerned by the facts detailed in the FDA’s adverse event reporting associated with Gardasil.  Merck has waged an aggressive lobbying campaign with state governments to mandate this HPV vaccine for young girls.  Given all the questions about Gardasil, the best public health policy would be to reevaluate its safety and to prohibit its distribution to minors.  In the least, governments should rethink any efforts to mandate or promote this vaccine for children

Merck Dr. Exposes Gardasil Scandal: Ineffective, Deadly, Very Profitable
APRIL 21, 2014
A controversial government-backed cervical cancer vaccine is ineffective, has deadly side effects and serves no other purpose than to generate profit for its manufacturer, according to a physician who worked at the major pharmaceutical company that’s made huge profits selling it to girls and young women.
It marks the most disturbing inside information exposed about the vaccine, Gardasil, which is manufactured by pharmaceutical giant Merck. The vaccine was scandalously fast-tracked by the Food and Drug Administration (FDA) and has been ardently promoted by the Obama administration as a miracle shot that can prevent certain strains of cervical cancer caused by Human Papillomavirus (HPV).
Instead it’s been linked to thousands of debilitating side effects, according to the government’s own daunting statistics. Since 2007 Judicial Watch has been investigating the Gardasil scandal and exposed droves of government records documenting thousands of adverse reactions associated with the vaccine, including paralysis, convulsions, blindness and dozens of deaths. Based on the records JW published a special report in 2008 detailing Gardasil’s approval process, side effects, safety concerns and marketing practices. Undoubtedly, it illustrates a large-scale public health experiment.
Now a one-time pharmaceutical industry physician, Dr. Bernard Dalbergue, who worked with Merck has come forth with shocking inside information that confirms what JW has exposed about Gardasil in its ongoing investigation. Dr. Dalbergue delivered the details in a French health magazine and a U.S. counterpart called Health Impact News Daily translated excerpts of the interview.

HPV NY Court Complaint

Robert F. Kennedy Jr Drops Vaccine Truth Bomb Live On TV
April 24, 2017 Baxter Dmitry
Robert F. Kennedy Jr. dropped a truth bomb live on TV this week, defying Big Pharma and corrupt mainstream media by sharing real facts about vaccine safety.
Explaining to Tucker Carlson that this was only the second time he had ever been allowed to talk about vaccine safety on TV, Robert F. Kennedy Jr. launched into a powerful attack on the vaccine industry, comparing it to a lawless mafia state.
“The pharmaceutical industry is so powerful,” he explained. “They give $5.4 billion a year to the media. They’ve gotten rid of the lawyers, so there is no legal interest in those cases. They have really been able to control the debate and silence people like me.“
Asked how things could get this bad, Robert F. Kennedy Jr. explained that in 1989 Congress granted Big Pharma “blanket legal immunity” when it comes to vaccines.
Big Pharma became a law unto themselves. They can put toxic ingredients in your vaccines, they can seriously injure your child – but you cannot sue them.
“What you have to understand is that the vaccine regimen changed dramatically around 1989. The reason it changed, Tucker, is that Congress, drowning in pharmaceutical industry money, did something they have never done for any other industry – they gave blanket legal immunity to all the vaccine companies.
“So that no matter how sloppy the line protocols, no matter how absent the quality control, no matter how toxic the ingredients, or egregious the injury to your child, you cannot sue them.

Autism and the MMR Vaccine: The Most Diabolical Medical Scandal of the Century
By Tami Canal On April 2, 2016
The following contains unsolicited adverse reaction reports associated with the MMR. Sadly, this is typical of the daily emails received by the ThinkTwice Global Vaccine Institute:
1. [MMR114] My 12-month-old received his MMR shot on a Friday. The following Friday he had a 104 degree temperature and became violently ill. The doctor said it was a stomach virus. But on Monday morning he woke up with a rash all over. I took him to the doctor and was very upset to learn that this is very common.
2. [MMR176] My friend’s 15-month-old daughter received an MMR vaccine. Within eight days she was hospitalized with a 104 degree fever and a skin rash. My friend called to see what I could find out about Stevens-Johnson syndrome. They told her that her daughter may die as a result of this.
3. [MMR203] A dear friend lost her 15-month old daughter two weeks after her MMR. She was healthy and showed no signs of illness yet died suddenly in her sleep one afternoon. The post mortem revealed a viral infection and traces of pneumonia, but her mother and I find it very hard to believe that the vaccination wasn’t to blame.
4. [MMR216] Three days ago my friend’s 15-month-old daughter was hospitalized after experiencing a high fever and her first seizure. The hospital put the baby through a series of tests, including a CAT scan and CBC. My friend told me he thought it was a reaction to the MMR vaccine she recently received. However, the doctors were puzzled as to the cause and disallowed this explanation.
5. [MMR317] Our son developed seizures after his MMR vaccine at 14 months. Today, after two years of anti-epilepsy medications, he has totally regressed. We decided to stop all medications five weeks ago and his grand mal fits have stopped. We are now left with a child experiencing severe constipation and bowel problems.
6. [MMR398] My daughter had a serious reaction to the MMR shot when she was 22 months. She developed brain damage after a fever of 106 degrees. She also has seizures which are unresponsive to medication, damage to the nerves of her eyes, and learning disabilities that she battles every day. We took her case to court and lost. The doctor who testified on their behalf stated that the government only called him in when they wanted a finding in their favor. What a setup! Of course they don’t have to live with the frustrations and expense of raising these vaccine-damaged children.
7. [MMR588] I was told by the nursing school where I am enrolled, “No vaccine, no school.” Even though I had all the normal vaccines as a child, I was unable to show this. Five days after I received the MMR vaccine, I was so ill that I ended up in the emergency room. The doctor told me that the MMR did not cause my sickness, and my nursing school supervisor said it was a virus. Why does the medical establishment deny vaccine reactions? Why can’t they tell us this important information and let us make educated responsible decisions. The irony is that I got the vaccine and now I’m so sick that I can’t go to school.

“The drug company that makes the MMR vaccine publishes an extensive list of warnings, contraindications, and adverse reactions associated with this triple shot. These may be found in the [MMR] vaccine package insert available from any doctor giving MMR, and in the Physician’s Desk Reference (PDR) at the library. The following afflictions affecting nearly every body system — blood, lymphatic, digestive, cardiovascular, immune, nervous, respiratory, and sensory — have been reported following receipt of the MMR shot: encephalitis, encephalopathy, neurological disorders, seizure disorders, convulsions, learning disabilities, subacute sclerosing panencephalitis (SSPE), demyelination of the nerve sheaths, Guillain-Barre’ syndrome (paralysis), muscle incoordination, deafness, panniculitis, vasculitis, optic neuritis (including partial or total blindness), retinitis, otitis media, bronchial spasms, fever, headache, joint pain, arthritis (acute and chronic), transverse myelitis, thrombocytopenia (blood clotting disorders and spontaneous bleeding), anaphylaxis (severe allergic reactions), lymphadenopathy, leukocytosis, pneumonitis, Stevens-Johnson syndrome, erythema multiforme, urticaria, pancreatitis, parotitis, inflammatory bowel disease, Crohn’s disease, ulcerative colitis, meningitis, diabetes, autism, immune system disorders, and death.”

Vaccine News – Vaccine-Autism Link Study is Allegedly Part of Trump Administration’s $54 Billion Budget Cut

Vaccine-Autism Link Study is Allegedly Part of Trump Administration’s $54 Billion Budget Cut
Regin OlimberioMar 13, 2017 12:50 AM EDT
President Donald Trump’s stance to study the alleged link between vaccine and autism stirs fear of hampered study and minimal funding among health sector. A previous study has already debunked the myth that vaccines can cause autism but Trump opened the doors to further research. Advocates of mass vaccination fear that they have to turn their energy defending vaccines instead of moving forward with a medical breakthrough.
To recall, the renewed vigor started in 2008 when the National Vaccine Advisory Committee pushed for a safety agenda about the issue. Parents were assured of transparent access to results of research about vaccine’s link to autism. The agenda resurged at the start of Trump administration.
Health experts argued that Trump’s policy might delay or hamper the administration of vaccines. By doing so, children will be more susceptible to natural infections. This heightened risk can occur even at small delay between vaccine shots.
Another implication could be the difficulty in availing health insurance being stipulated under Affordable Care Act or Obamacare. The said law assures health coverage for pre-existing condition. Health insurance companies can simply imply that autism is not part of coverage since it is debatably not pre-existing but aggravated by vaccines. Another law that will suffer a setback is Disabilities Education Act that ensures education for autistic children, Live Science reported.

Vaccines and Autism Revisited — The Hannah Poling Case
Paul A. Offit, M.D. N Engl J Med 2008
On April 11, 2008, the National Vaccine Advisory Committee took an unusual step: in the name of transparency, trust, and collaboration, it asked members of the public to help set its vaccine-safety research agenda for the next 5 years. Several parents, given this opportunity, expressed concern that vaccines might cause autism — a fear that had recently been fueled by extensive media coverage of a press conference involving a 9-year-old girl named Hannah Poling.
When she was 19 months old, Hannah, the daughter of Jon and Terry Poling, received five vaccines — diphtheria–tetanus–acellular pertussis, Haemophilus influenzae type b (Hib), measles–mumps–rubella (MMR), varicella, and inactivated polio. At the time, Hannah was interactive, playful, and communicative. Two days later, she was lethargic, irritable, and febrile. Ten days after vaccination, she developed a rash consistent with vaccine-induced varicella.
Months later, with delays in neurologic and psychological development, Hannah was diagnosed with encephalopathy caused by a mitochondrial enzyme deficit. Hannah’s signs included problems with language, communication, and behavior — all features of autism spectrum disorder. Although it is not unusual for children with mitochondrial enzyme deficiencies to develop neurologic signs between their first and second years of life, Hannah’s parents believed that vaccines had triggered her encephalopathy. They sued the Department of Health and Human Services (DHHS) for compensation under the Vaccine Injury Compensation Program (VICP) and won.
On March 6, 2008, the Polings took their case to the public. Standing before a bank of microphones from several major news organizations, Jon Poling said that “the results in this case may well signify a landmark decision with children developing autism following vaccinations.”1 For years, federal health agencies and professional organizations had reassured the public that vaccines didn’t cause autism. Now, with DHHS making this concession in a federal claims court, the government appeared to be saying exactly the opposite. Caught in the middle, clinicians were at a loss to explain the reasoning behind the VICP’s decision.
The Poling case is best understood in the context of the decision-making process of this unusual vaccine court. In the late 1970s and early 1980s, American lawyers successfully sued pharmaceutical companies claiming that vaccines caused a variety of illnesses, including unexplained coma, sudden infant death syndrome, Reye’s syndrome, transverse myelitis, mental retardation, and epilepsy. By 1986, all but one manufacturer of the diphtheria–tetanus–pertussis vaccine had left the market. The federal government stepped in, passing the National Childhood Vaccine Injury Act, which included the creation of the VICP. Funded by a federal excise tax on each dose of vaccine, the VICP compiled a list of compensable injuries. If scientific studies supported the notion that vaccines caused an adverse event — such as thrombocytopenia after receipt of measles-containing vaccine or paralysis after receipt of oral polio vaccine — children and their families were compensated quickly, generously, and fairly. The number of lawsuits against vaccine makers decreased dramatically.

Whooping cough increase related to current vaccine
Friday, 24 April 2015 Dani Cooper ABC
The move to an artificially created vaccine for whooping cough is behind an increase in cases of the deadly disease in the US, a new study suggests.
The findings highlight the need to do similar research in Australia where whooping cough cases have spiralled upward in the past decade, co-author Associate Professor Manoj Gambhir, from the University of Monash, says.
In 2012 the US saw the highest number of pertussis (whooping cough) cases since 1955.
At the same time there has been a shift in the age group reporting the largest number of cases from adolescents to 7 to 11 year olds.
In the paper, published today in PLOS Computational Biology, Gambhir and colleagues use mathematical modelling of 60 years of pertussis disease data to determine what best explains this increase.
Their research finds the level of protection of the currently used acellular vaccine is lower than that of the previously used whole-cell vaccine.
Gambhir says the original whole-cell vaccine developed in 1942 was very effective.
Following introduction of vaccination, the reported disease incidence in the US dropped from 150 cases per 100,000 each year before 1940, to the point of near elimination in the mid-1970s when there were just 0.5 reported cases per 100,000 population.
“Now in the past decade we have seen a rise from that low to about 10-20 cases per 100,000,” says Gambhir.
Gambhir, who led the study with Dr Thomas Clark at the Centers for Disease Control and Prevention, in Atlanta, Georgia, and Professor Neil Ferguson, of the Imperial College London in the UK, says while the number of cases remains low the trend is upward.
“It’s the sort of five-year by five-year rise that is the concern because the worry is it could go back to those levels at which we would start seeing infant deaths,” he says.
New vaccine to blame
Gambhir says in 1991 researchers developed a new vaccine to address public concerns that the whooping cough vaccine caused a reaction in some children.

Study – A Change in Vaccine Efficacy and Duration of Protection Explains Recent Rises in Pertussis Incidence in the United States
Published: April 23, 2015
PDF version
Abstract
Over the past ten years the incidence of pertussis in the United States (U.S.) has risen steadily, with 2012 seeing the highest case number since 1955. There has also been a shift over the same time period in the age group reporting the largest number of cases (aside from infants), from adolescents to 7–11 year olds. We use epidemiological modelling and a large case incidence dataset to explain the upsurge. We investigate several hypotheses for the upsurge in pertussis cases by fitting a suite of dynamic epidemiological models to incidence data from the National Notifiable Disease Surveillance System (NNDSS) between 1990–2009, as well as incidence data from a variety of sources from 1950–1989. We find that: the best-fitting model is one in which vaccine efficacy and duration of protection of the acellular pertussis (aP) vaccine is lower than that of the whole-cell (wP) vaccine, (efficacy of the first three doses 80% [95% CI: 78%, 82%] versus 90% [95% CI: 87%, 94%]), increasing the rate at which disease is reported to NNDSS is not sufficient to explain the upsurge and 3) 2010–2012 disease incidence is predicted well. In this study, we use all available U.S. surveillance data to: 1) fit a set of mathematical models and determine which best explains these data and 2) determine the epidemiological and vaccine-related parameter values of this model. We find evidence of a difference in efficacy and duration of protection between the two vaccine types, wP and aP (aP efficacy and duration lower than wP). Future refinement of the model presented here will allow for an exploration of alternative vaccination strategies such as different age-spacings, further booster doses, and cocooning.

Vaccine Detox: Do This IMMEDIATELY if Baby Regresses after Shots
by Sarah Updated: December 23, 2016
When it comes to childhood immunizations, the approach with the least long term risk to your child’s health is refusing the shots in the first place. It’s a better strategy to avoid the myriad of vaccine related health problems from the start rather than scrambling for an effective vaccine detox to unwind the immune system damage later.
You can always get vaccinated, but undoing vaccine damage is a challenging process. Procrastination is a virtue when it comes to shots!
Science is not on your side if you choose to vaccinate, contrary to the drone of government officials, the media, misinformed school officials, and even pediatricians, some of whom are fearful of reprisal if they speak out with a differing opinion on the subject.
Emergency Vaccine Detox if a Child Regresses after Vaccination
Loss of eye contact, unresponsiveness to sounds or other stimuli, and the sudden inability to walk are common observations by parents of young children after a round of vaccinations. They are so common, in fact, that more than 1 in 50 children is currently on the autistic spectrum. This is up from one in every 300 children when my first child was born in 1998. In the 1980s, about 1 in every 10,000 children was autistic. Scientific projections are that 1 in every 2 boys will be on the spectrum by 2030 at the current rate of growth.
What should you do if you decide to vaccinate and your child suddenly starts to regress?
Developmental pediatrician Dr. Mary Megson of the University of Virginia has answers for you based on her extensive clinical experience treating autistic children for over 25 years.
Dr. Megson has developed a framework for treating autism based on the piece of the puzzle she has discovered clinically – blocked Vitamin A pathways in the brain.

Six Reasons To Say NO to Vaccination
by Sarah Updated: February 25, 2017
Vaccination is an extremely controversial topic these days. Whatever side of the aisle you may fall with regard to your opinion about vaccination, one thing is for certain. The choice to vaccinate or not vaccinate is a decision that has the potential to greatly impact the health of you and most importantly, your children for the rest of their lives.
As a result, this decision should not be taken lightly and it should not be made in a vacuum.   In other words, don’t just take your pediatrician’s word that shots are safe.    It is possible for doctors to be wrong.    They are human, after all.   In reality, your doctor is simply parroting the standard line about vaccination from the American Medical Association (AMA) playbook.    If you think you are getting their honest assessment, think again.
You should neither assume shots are dangerous just because your friend down the street doesn’t vaccinate her kids.

#1:   Pharmaceutical Companies Can’t Be Trusted (Ever)
#2:   ALL Vaccines are Loaded with Chemicals and Heavy Metals
#3:   Vaccinated Children are the Unhealthiest, Most Chronically Sick Children
#4:   Other Countries Are Waking Up to the Dangers of Vaccination
#5:   Numerous Vaccines Have Already Had Problems/Been Removed from the Market
#6   You Can Always Get Vaccinated, But You Can Never Undo a Vaccination

Govt. Still Pushing HPV Vaccine on Kids a Decade after JW Exposed Deadly Side Effects
MARCH 09, 2017
A decade after Judicial Watch exposed the dangers of a government-backed cervical cancer vaccine, a federal lawsuit highlights its perilous side effects including paralysis, seizures, nausea and death. Litigation was initiated by disgruntled parents because the government is still pushing the hazardous vaccine, manufactured by pharmaceutical giant Merck, on children as young as nine years old to treat a sexually transmitted disease.
The vaccine is called Gardasil and in the last ten years Judicial Watch has uncovered troves of government records documenting its harmful side effects. The vaccine was scandalously fast-tracked by the Food and Drug Administration (FDA) and was ardently promoted by the Obama administration as a miracle shot that can prevent certain strains of cervical cancer caused by Human Papillomavirus (HPV). Instead it’s been linked to thousands of debilitating side effects, according to the government’s own daunting statistics. This includes thousands of cases of paralysis, convulsions, blindness and dozens of deaths. Back in 2008, after receiving the first disturbing batch of records from the Centers for Disease Control and Prevention (CDC), Judicial Watch published a special report detailing Gardasil’s approval process, side effects, safety concerns and marketing practices. Undoubtedly, it illustrates a large-scale public health experiment.
Regardless, the government has continued promoting the vaccine while covering up its debilitating side effects, recommending it for girls—and more recently boys—starting at age 9. The Obama administration gave dozens of state and municipal health agencies tens of millions of dollars to boost the number of adolescents that get Gardasil. This includes targeting low-income and ethnic minority populations that receive “culturally sensitive” intervention in a variety of languages, including Spanish, Mandarin, Armenian and Korean. U.S. law forbids lawsuits against vaccine manufacturers, but Judicial Watch has obtained records from the Department of Health and Human Services (HHS) revealing that its National Vaccine Injury Compensation Program (VICP) has awarded nearly $6 million to dozens of victims in claims made against the very HPV vaccine it is pushing on children.
In 2014 a physician who worked at Merck denounced Gardasil as an ineffective vaccine with deadly side effects that serves no other purpose than to generate profit for its manufacturer. The former pharmaceutical industry doctor, Bernard Dalbergue, said Gardasil is useless, costs a fortune and that decision-makers at all levels are aware of it. “I predict that Gardasil will become the greatest medical scandal of all times because at some point in time, the evidence will add up to prove that this vaccine, technical and scientific feat that it may be, has absolutely no effect on cervical cancer and that all the very many adverse effects which destroy lives and even kill, serve no other purpose than to generate profit for the manufacturers,” Dr. Dalbergue said. He added that there is far too much financial interest for the vaccine to be withdrawn. Dr. Dalbergue’s statements were used by a member of the French Parliament as part of a broader campaign blasting Gardasil’s horrible safety record in Europe.

New FDA Records Obtained by Judicial Watch Indicate 28 Deaths Related to Gardasil in 2008
JUNE 22, 2009
Judicial Watch, the public interest group that investigates and prosecutes government corruption, announced today that it has obtained records from the Food and Drug Administration (FDA) documenting 28 deaths in 2008 associated with Gardasil, the vaccination for human papillomavirus (HPV), up from 19 deaths in 2007. The total number of Gardasil-related deaths is 47 since the vaccine was approved in 2006. Overall, the FDA documented 6,723 “adverse events” related to Gardasil in 2008, of which 1,061 were considered “serious,” and 142 considered “life threatening.”
The following are several “adverse events” documented by the FDA’s Vaccine Adverse Event Reporting System (VAERS):
“15 months from the completion of the GARDASIL HPV vaccination, I had full blown cervical cancer. My oncologist would like to do a hysterectomy at this time, but [as I have] always wanted children, I have chosen to wait . . . I have two of the [strains] that the shot is suppose to prevent . . . I now have cervical cancer and I am left wondering what role the GARDASIL HPV vaccination played in the hasty onset.” (ID: 319836)
“After receiving her second dose of GARDASIL … she could crawl but … needed to use crutches or a wheel chair … She was experienced problems breathing and had ‘super migraines’ that never went away … She had swelling in her face, jaw and wrists. The patient was diagnosed with GUILLAIN-BARRE syndrome, myelin sheath degeneration and peripheral neuropathy. Patient was hospitalized twice … patient has not recovered from symptoms.” (ID: 318052)
A 19-year-old girl with no medical history immediately experienced side effects after receiving the Gardasil vaccine. Within eleven days her symptoms included “Aggression, Arthralgia, Complex partial seizures, Confusional state, Convulsion, Crying, Dizziness, Epilepsy, Fatigue, Feeling abnormal, Grand mal convulsion, Immediate post-injection reaction, Irritability, Myalgia, Nausea, Pain, Postictal state, Somnolence, Syncope, Tremor, and Unresponsive to stimuli.” (ID: 320598)
“Two weeks after the third dose, the patient developed a complication. She was taken to the hospital by ambulance but passed away during the transport from an unknown cause…Upon arrival in ER unresponsive, pupils fixed and dilated, no cardiac activity. Resuscitation unsuccessful and patient expired.” (ID: 314769)
The FDA VAERS reports show that since last June, 235 cases detailed permanent disability. There were also 29 new cases of Guillain-Barre Syndrome, and 147 cases of “spontaneous abortions,” or miscarriages, when the vaccine was given to pregnant women.

Merck Dr. Exposes Gardasil Scandal: Ineffective, Deadly, Very Profitable
APRIL 21, 2014
A controversial government-backed cervical cancer vaccine is ineffective, has deadly side effects and serves no other purpose than to generate profit for its manufacturer, according to a physician who worked at the major pharmaceutical company that’s made huge profits selling it to girls and young women.
It marks the most disturbing inside information exposed about the vaccine, Gardasil, which is manufactured by pharmaceutical giant Merck. The vaccine was scandalously fast-tracked by the Food and Drug Administration (FDA) and has been ardently promoted by the Obama administration as a miracle shot that can prevent certain strains of cervical cancer caused by Human Papillomavirus (HPV).
Instead it’s been linked to thousands of debilitating side effects, according to the government’s own daunting statistics. Since 2007 Judicial Watch has been investigating the Gardasil scandal and exposed droves of government records documenting thousands of adverse reactions associated with the vaccine, including paralysis, convulsions, blindness and dozens of deaths. Based on the records JW published a special report in 2008 detailing Gardasil’s approval process, side effects, safety concerns and marketing practices. Undoubtedly, it illustrates a large-scale public health experiment.
Now a one-time pharmaceutical industry physician, Dr. Bernard Dalbergue, who worked with Merck has come forth with shocking inside information that confirms what JW has exposed about Gardasil in its ongoing investigation. Dr. Dalbergue delivered the details in a French health magazine and a U.S. counterpart called Health Impact News Daily translated excerpts of the interview.
The physician confirms that Gardasil is useless, costs a fortune and that decision-makers at all levels are aware of it. “I predict that Gardasil will become the greatest medical scandal of all times because at some point in time, the evidence will add up to prove that this vaccine, technical and scientific feat that it may be, has absolutely no effect on cervical cancer and that all the very many adverse effects which destroy lives and even kill, serve no other purpose than to generate profit for the manufacturers,” Dr. Dalbergue says. He adds that there is far too much financial interest or the vaccine to be withdrawn.

Examining the FDA’s HPV Vaccine Records: PDF source
Detailing the Approval Process, Side-Effects, Safety Concerns and Marketing Practices of a Large-Scale Public Health Experiment June 30, 2008

Push for nation-wide ‘no jab, no play’ at childcare centres
11:40pm March 12, 2017
Unvaccinated children could be banned from attending childcare centres and preschools across Australia as part of a renewed push by the federal government.
Prime Minister Malcolm Turnbull has written to state and territory leaders in a move towards introducing consistent laws to protect children across the country.
“If you don’t vaccinate your child you are not just putting their own life at risk, but you are putting everyone else’s children at risk,” Mr Turnbull wrote.

Settlement for Saba Button, severely disabled after flu vaccine
Updated 8 Jun 2014, 2:26am
The family of a West Australian child left severely disabled after receiving a flu jab has reached a settlement with the vaccine’s manufacturer and the State Government.
Saba Button suffered brain and organ damage after getting the Fluvax shot when she was 11 months old in 2010.
Her parents launched legal action in the Federal Court against the vaccine’s manufacturer, CSL Limited.
CSL cross-claimed against the State of WA and the Health Minister.
All parties have reached a confidential settlement which has today been accepted by Federal Court Justice Michael Barker.
Saba’s father, Mick Button, said it had been a long battle for compensation.
“Today is a bittersweet feeling for us,” he said.
“It’s a relief to have the legal case behind us.
“We now have the ability to be able to supply Saba with the care, the therapy, the equipment, all the things that she needs to give her the best quality of life.”
Her mother Kirsten Button said she was relieved the legal action had been finalised.
“It doesn’t matter how much you have because you can’t buy your health but it is a good outcome, and the fact that it’s settled, we’re quite a strong family and we have moved forward but I think having that hanging over your head as such can be stressful so now we can move forward knowing that it’s all over.”
Mr Button said the funds would help Saba continue ongoing therapy and explore new options both in Australia and overseas.
“This doesn’t just stop now, once all the cameras are gone, it’s back to business and we’ve got a lot to do with Saba,” he said.

VACCINE STUDY: Peer-reviewed study shows vaccinated children have a 700% higher chance of neurodevelopmental disorder
Tuesday, March 07, 2017 by: Vicki Batts
(Natural News) On Valentine’s Day, a 34-page study that illustrated some of the harmful effects of vaccination was made available for viewing online. Six hours later, the URL had vanished, and the study was seemingly erased from the depths of the internet — likely in the hopes that the “controversial” information it contained would be forgotten.
Vaccination and Health Outcomes: A Survey of 6- to 12-year-old Vaccinated and Unvaccinated Children based on Mothers’ Reports, by Anthony R. Mawson, et al. seemed like any other standard report on vaccination at first glance, according to author James Grundvig. The paper had been linked to Grundvig, and he recently published an article about the study, how he authenticated it with the study’s author, and he even described how the publishing journal went about censoring the information.
Grundvig writes that after reading Mawson’s conclusions in the study, it appears that perhaps the CDC has purposefully avoided conducting such research themselves because “it would have run counter to CDC’s messaging that all ‘vaccines are safe.’”
Research: vaccines and neurodevelopmental disorders
To conduct their research, Mawson and his team engaged in a cross-sectional survey of mothers of children who were educated at home. Homeschooling organizations from Florida, Louisiana, Mississippi, and Oregon were asked to forward an email to their members, requesting mothers to fill out an anonymous online survey. The questionnaire gathered information on vaccination status and health outcomes of their biological children who were between the ages of 6 and 12. In total, 415 mothers provided information about 666 children. Of those, just 261 (or 39 percent) had not been vaccinated. Information on pregnancy experiences, birth histories, acute and chronic conditions, and the usage of medication and health care services was also included in the data collection.
Overall, the results of the study showed that while vaccinated children were less likely to have had chicken pox or pertussis, they were significantly more likely to develop other types of infections, allergies, and were more likely to be diagnosed with a neurodevelopmental disorder (referred to in the study as an NDD). NDDs were defined as autism spectrum disorders, attention deficit hyperactivity disorder (ADHD), a learning disability, or any combination of the three. Could it be that unvaccinated children are in many ways healthier? It certainly seems that way.
Data reveals shocking disparities

First Peer-Reviewed Study of Vaccinated versus Unvaccinated Children (Censored by an International Scientific Journal) Now Public
Results: Vaccinated children were significantly less likely than the unvaccinated to have been diagnosed with chickenpox and pertussis, but significantly more likely to have been diagnosed with other infections, allergies and NDDs (defined as Autism Spectrum Disorder, Attention Deficit Hyperactivity Disorder, and/or a learning disability).
Chronic Illness Detail:
Vaccinated children were significantly more likely than the unvaccinated to have been diagnosed with the following chronic illnesses:
7-fold higher odds of any neurodevelopmental disorder (i.e., learning disability, ADHD, or ASD)

        2-fold increase in Autism Spectrum Disorder (“ASD”)
2-fold increase in ADHD
2-fold increase in learning disabilities
1-fold increase in allergic rhinitis
9-fold increase in other allergies
9-fold increase in eczema/atopic dermatitis
4-fold increase in any chronic 
illness

No significant differences were observed with regard to cancer, chronic fatigue, conduct disorder, Crohn’s disease, depression, Types 1 or 2 diabetes, encephalopathy, epilepsy, hearing loss, high blood pressure, inflammatory bowel disease, juvenile rheumatoid arthritis, obesity, seizures, and Tourette’s syndrome. However, larger samples would be needed to detect group differences in these less common conditions.
Acute Illness Detail:
Vaccinated children were significantly less likely than unvaccinated children to have had chickenpox or whooping cough (p<0.001).
Vaccinated children had a 3.8-fold increased odds of middle ear infections and a 5.9-fold increased odds of being diagnosed with pneumonia compared to unvaccinated children.
No significant differences were seen between the two groups with regard to Hepatitis A or B, high fever in the past 6 months, measles, mumps, meningitis (viral or bacterial), influenza, or rotavirus.

US Immunization Schedule Recommends 26 Vaccinations For Children Under 1, Highest In World And Ranks 34th In Infant Mortality
Print Friendly MARCH 12, 2017
A new study published today in the Journal of Human and Experimental Toxology found that countries that administer a higher number of vaccines during the first year of life experience higher infant mortality rates.
The infant mortality rate (IMR) of a country is one of the most accepted and critical indicators of the socioeconomic well being of its citizens. It also reflects public health conditions and whether those conditions are improving or worsening over time.
The United States ranks 34th in infant mortality rate which means that 33 countries outrank the USA in this critical measure of public health. In addition, the United States’ immunization schedule for infants under 1 year of age recommends 26 vaccinations – the highest in the entire world.

Vaccine pioneer admits adding cancer-causing virus to Vaccine

Vaccine pioneer admits adding cancer-causing virus to Vaccine
In this interview Dr. Maurice Hilleman reveals some astounding revelations. He admits that Merck drug company vaccines (Polio) had been deliberately contaminated with SV40, a cancer-causing monkey virus from 1953 – 63.
For years, researchers suggested that millions of vials of polio vaccine, contaminated with SV40, infected individuals which caused human tumors, and by 1999, molecular evidence of SV40 infections were showing up in children born after 1982. Some experts now suggest the virus may have remained in the polio vaccine until as late as 1999.
In 2002, the journal Lancet published compelling evidence that contaminated polio vaccine was responsible for up to half of the 55,000 non-Hodgkin’s lymphoma cases that were occurring each year. And there is the likelihood that there was an importing and spreading of the AIDS virus in the same manner, as revealed in the video.
At first no one could fathom how the virus had been transmitted into the human population, but this shocking video proves that it was deliberately added to the vaccine by Dr. Maurice Hilleman, which was “good science” at that time.
Just Who is Dr. Maurice Hilleman?
Now, for those of you who may think Dr. Hilleman was just another crackpot (he passed away in 2005), think again. He was, and still is, the leading vaccine pioneer in the history of vaccines. He developed more than three dozen vaccines—more than any other scientist in history—and was the developer of Merck’s vaccine program.
He was a member of the U.S. National Academy of Science, the Institute of Medicine, the American Academy of Arts and Sciences, and the American Philosophical Society, and received a special lifetime achievement award from the World Health Organization.
When he was chief of the Department of Respiratory Diseases with what’s now the Walter Reed Army Institute of Research, he discovered the genetic changes that occur when the influenza virus mutates, known as shift and drift. He was also one of the early vaccine pioneers to warn about the possibility that simian viruses might contaminate vaccines.So Dr. Hilleman knew what he was talking about. And in his own words, “vaccines have to be considered the bargain basement technology for the 20th Century.”

CDC admits 98 million Americans were given cancer virus via the polio shot
The CDC has admitted that between 1955–1963 over 98 million Americans received one or more doses of a polio shot which was contaminated with a cancer-causing virus called Simian vacuolating virus 40 (SV40).  The CDC quickly took down the page, along with Google, but the site was luckily cached and saved to symbolize this grand admission.

Historical Vaccine Safety Concerns
Simian Virus 40(SV40) – 1955-1963
Some of the polio vaccine administered from 1955 to 1963 was contaminated with a virus called simian virus 40 (SV40). The virus came from the monkey kidney cells used to produce the vaccines.  Once the contamination was discovered in the Salk inactivated polio vaccine in use at that time, the U.S. government established requirements for vaccine testing to verify that all new batches of the polio vaccine were free of SV40. Because of research done with SV40 in animal models, there was some concern that the virus could cause cancer. However, evidence suggests that SV40 has not caused cancer in humans.

Volume 3, Number 2—June 1997
Simian Virus 40 (SV40), a Possible Human Polyomavirus (Workshop Held at NIH)
During the past 4 years, polymerase chain reaction (PCR) assays have detected DNA sequences related to SV40 (an oncogenic simian polyomavirus) in a variety of human tissues, especially choroid plexus tumors, ependymomas, mesotheliomas, and osteosarcomas (1-7). These findings were supported by the isolation of infectious SV40 from a choroid plexus tumor (8).
Although another paper reported the failure to detect SV40 DNA in mesotheliomas (9), these studies have reawakened interest in inadvertent human exposure to SV40 in the late 1950s and early 1960s when polio and adenovirus vaccines prepared in rhesus monkey cells containing SV40 were used (10,11). In response to the implications of detecting SV40 DNA in human tumors, the Food and Drug Administration, National Institutes of Health, National Vaccine Program Office, and Centers for Disease Control and Prevention sponsored a workshop on SV40 on January 27-28, 1997 at the National Institutes of Health to examine the possibility that SV40 is an infectious agent in humans.

The following statement is an introduction for a more detailed packet on SV-40 and animal viruses in the production of vaccines.

Statement by Barbara Loe Fisher, Co-Founder & President
National Vaccine Information Center
Workshop on Simian Virus-40 (SV-40): A Possible Human Polyomavirus
January 27-28, 1997
Bethesda, Maryland
The National Vaccine Information Center (NVIC), which was founded in 1982 and represents health care consumers and health care professionals concerned about vaccine safety, became actively involved in 1994 in researching reports of contamination of childhood vaccines with animal viruses and the possibility that inter-species transfer of animal viruses into humans via vaccines has had a negative impact on public health. Our concern was that government health agencies and industry had not adequately addressed many of the most important questions that remained unanswered about the contamination of polio vaccines with simian (monkey) viruses.

Should I Get the Flu Shot? CDC Data Raise Concerns

Should I Get the Flu Shot? CDC Data Raise Concerns
In February the CDC revealed that the 2014-2015 influenza vaccine had an efficacy rate of only 19 percent. If that was not bad enough, in June the CDC’s committee that advises on immunization practices announced that nasal spray flu vaccines should not be used in the 2016-2017 flu season because, in the CDC’s own words, “no protective benefit could be measured” from taking them.
Indeed, numerous peer-reviewed scientific studies have shown that the flu vaccine is not effective either at reducing the flu or reducing flu-related deaths.
When a team of researchers at the National Institutes of Health compared flu vaccine rates with influenza-related illness over a 19-year period, from 1980 to 1999, they found that deaths from the flu increased as vaccination rates increased. “In conclusion, the increase in elderly influenza vaccination coverage in the U.S. after 1980 was not accompanied by a decline in influenza-related mortality,” the researchers concluded.
A study, led by a researcher at the National Institute of Allergy and Infectious Diseases and published in the journal Archives of Internal Medicine, found that increasing vaccination coverage did not correlate with declining mortality and the decline in influenza-related mortality could not be attributed to the flu vaccine but was rather the result of naturally acquired immunity. Observational studies crediting the flu vaccine with contributing to decreased deaths from the flu, “substantially overestimate vaccination benefit,” these researchers concluded.
A study published in the American Journal of Perinatology of vaccine effectiveness in pregnant women in Northern California across five flu seasons found that women who received flu vaccines during pregnancy had the same risk for influenza-like illness as unvaccinated women, and infants born to women who received flu vaccines also had the same risks for influenza or pneumonia as infants born to unvaccinated women. In other words, vaccine status made no difference to whether or not pregnant women or their offspring got the flu.
A study published in Pediatrics International of Japanese children ages 6 months to 2 years who were vaccinated against the flu found that the influenza vaccine did not reduce the rate of influenza A infections in children under two.

CDC Presents Updated Estimates of Flu Vaccine Effectiveness for the 2014-2015 Season
Flu vaccine did not protect against drifted H3N2 viruses, but protected against vaccine-like H3N2 and B viruses
On February 26, 2015, updated interim influenza (flu) vaccine effectiveness (VE) estimates for the current 2014-2015 season were presented to the Advisory Committee on Immunization Practices (ACIP). The updated VE estimate against influenza A H3N2 viruses was 18% (95% confidence interval (CI): 6%-29%).This result is similar to the VE point estimate of 23%, which was reported in a January 16 Morbidity and Mortality Weekly Report (MMWR) and confirms reduced protection against H3N2 viruses this season. The VE estimate against influenza B viruses this season was 45% (95% CI: 14% – 65%).
How well the flu vaccine works can vary depending on a number of factors, including the similarity between circulating influenza viruses and vaccine viruses, and the age, health or immune status of the person vaccinated. The findings for VE against H3N2 viruses this season are about one-third of the VE expected when the flu vaccine is well matched to circulating influenza viruses. The VE against influenza B viruses this season is similar to the effectiveness observed when vaccine viruses and most circulating viruses are well matched.

ACIP votes down use of LAIV for 2016-2017 flu season
Media Statement
For Immediate Release: Wednesday, June 22, 2016
CDC’s Advisory Committee on Immunization Practices (ACIP) today voted that live attenuated influenza vaccine (LAIV), also known as the “nasal spray” flu vaccine, should not be used during the 2016-2017 flu season. ACIP continues to recommend annual flu vaccination, with either the inactivated influenza vaccine (IIV) or recombinant influenza vaccine (RIV), for everyone 6 months and older.
ACIP is a panel of immunization experts that advises the Centers for Disease Control and Prevention (CDC). This ACIP vote is based on data showing poor or relatively lower effectiveness of LAIV from 2013 through 2016.

Vaccine injury testimony – Gardasil – Hannah M. Robinson

Vaccine injury testimony – Gardasil – Hannah M. Robinson
My vaccine injury, I have several photos and videos I feel ready to upload… Just a very small part of it… Thanks Gardasil! If you have a popular public profile and wish to share this or are close to one of the “higher ups” in our groups please private message me so I can send it to you.

New Concerns about the Human Papillomavirus Vaccine
It has recently come to the attention of the College that one of the recommended vaccines could possibly be associated with the very rare but serious condition of premature ovarian failure (POF), also known as premature menopause.
American College of Pediatricians – January 2016
The American College of Pediatricians (The College) is committed to the health and well-being of children, including prevention of disease by vaccines. It has recently come to the attention of the College that one of the recommended vaccines could possibly be associated with the very rare but serious condition of premature ovarian failure (POF), also known as premature menopause. There have been two case report series (3 cases each) published since 2013 in which post-menarcheal adolescent girls developed laboratory documented POF within weeks to several years of receiving Gardasil, a four-strain human papillomavirus vaccine (HPV4).1,2 Adverse events that occur after vaccines are frequently not caused by the vaccine and there has not been a noticeable rise in POF cases in the last 9 years since HPV4 vaccine has been widely used.
Nevertheless there are legitimate concerns that should be addressed: (1) long-term ovarian function was not assessed in either the original rat safety studies3,4 or in the human vaccine trials, (2) most primary care physicians are probably unaware of a possible association between HPV4 and POF and may not consider reporting POF cases or prolonged amenorrhea (missing menstrual periods) to the Vaccine Adverse Event Reporting System (VAERS), (3) potential mechanisms of action have been postulated based on autoimmune associations with the aluminum adjuvant used1 and previously documented ovarian toxicity in rats from another component, polysorbate 80,2 and (4) since licensure of Gardasil® in 2006, there have been about 213 VAERS reports (per the publicly available CDC WONDER VAERS database) involving amenorrhea, POF or premature menopause, 88% of which have been associated with Gardasil®.5 The two-strain HPV2, CervarixTM, was licensed late in 2009 and accounts for 4.7 % of VAERS amenorrhea reports since 2006, and 8.5% of those reports from February 2010 through May 2015. This compares to the pre-HPV vaccine period from 1990 to 2006 during which no cases of POF or premature menopause and 32 cases of amenorrhea were reported to VAERS.
Many adolescent females are vaccinated with influenza, meningococcal, and tetanus vaccines without getting Gardasil®, and yet only 5.6% of reports related to ovarian dysfunction since 2006 are associated with such vaccines in the absence of simultaneous Gardasil® administration. The overwhelming majority (76%) of VAERS reports since 2006 with ovarian failure, premature menopause, and/or amenorrhea are associated solely with Gardasil®. When VAERS reports since 2006 are restricted to cases in which amenorrhea occurred for at least 4 months and is not associated with other known causes like polycystic ovary syndrome or pregnancy, 86/89 cases are associated with Gardasil®, 3/89 with CervarixTM, and 0/89 with other vaccines administered independently of an HPV vaccine.5 Using the same criteria, there are only 7 reports of amenorrhea from 1990 through 2005 and no more than 2 of those associated with any one vaccine type.
Few other vaccines besides Gardasil® that are administered in adolescence contain polysorbate 80.6 Pre-licensure safety trials for Gardasil® used placebo that contained polysorbate 80 as well as aluminum adjuvant.2,7 Therefore, if such ingredients could cause ovarian dysfunction, an increase in amenorrhea probably would not have been detected in the placebo controlled trials. Furthermore, a large number of girls in the original trials were taking hormonal contraceptives which can mask ovarian dysfunction including amenorrhea and ovarian failure.2 Thus a causal relationship between human papillomavirus vaccines (if not Gardasil® specifically) and ovarian dysfunction cannot be ruled out at this time.