Chicken pox vaccine associated with shingles epidemic

Chicken pox vaccine associated with shingles epidemic
Goldman’s research supports that shingles, which results in three times as many deaths and five times the number of hospitalizations as chicken pox, is suppressed naturally by occasional contact with chicken pox.
Dr. Goldman’s findings have corroborated other independent researchers who estimate that if chickenpox were to be nearly eradicated by vaccination, the higher number of shingles cases could continue in the U.S. for up to 50 years; and that while death rates from chickenpox are already very low, any deaths prevented by vaccination will be offset by deaths from increasing shingles disease. Another recent peer-reviewed article authored by Dr. Goldman and published in Vaccine presents a cost-benefit analysis of the universal chicken pox (varicella) vaccination program. Goldman points out that during a 50-year time span, there would be an estimated additional 14.6 million (42%) shingles cases among adults aged less than 50 years, presenting society with a substantial additional medical cost burden of $4.1 billion. This translates into $80 million annually, utilizing an estimated mean healthcare provider cost of $280 per shingles case.
After a child has had varicella (chickenpox), the virus becomes dormant and can reactivate later in adulthood in a closely related disease called shingles–both caused by the same varicella-zoster virus (VZV). It has long been known that adults receive natural boosting from contact with children infected with chicken pox that helps prevent the reactivation of shingles.
Based on Dr. Goldman’s earlier communications with the Centers for Disease Control and Prevention (CDC), Goldman maintains that epidemiologists from the CDC are hoping “any possible shingles epidemic associated with the chickenpox vaccine can be offset by treating adults with a ‘shingles’ vaccine.” This intervention would substitute for the boosting adults previously received naturally, especially during seasonal outbreaks of the formerly common childhood disease.

The Polio Vaccine Cancer Cover-up & Cancer risk associated with simian virus 40 contaminated polio vaccine

Cancer risk associated with simian virus 40 contaminated polio vaccine.
RESULTS:
Our analysis indicates increased rates of ependymomas (37%), osteogenic sarcomas (26%), other bone tumors (34%) and mesothelioma (90%) among those in the exposed as compared to the unexposed birth cohort.
CONCLUSIONS:
These data suggest that there may be an increased incidence of certain cancers among the 98 million persons exposed to contaminated polio vaccine in the U.S.; further investigations are clearly justified.

The Polio Vaccine Cancer Cover-up
The polio vaccines developed in the 1950s by Jonas Salk and Albert Sabin allegedly eradicated one of the most feared diseases of the 20th century. The media hailed the success of these vaccines as a modern day miracle. However, the polio story has a much darker side that has mostly been kept a secret.
Both Sabin’s live virus vaccine given orally and Salk’s inactivated virus vaccine given by injection were far from perfect. In fact, in 1955 the vaccine used in Berkley, California infected some 200 children, leaving several dead and many paralyzed. Yet this incident proved minor compared to what was later discovered.
In order to grow large quantities of the poliovirus, scientists needed to use Rhesus monkey kidney cells, which carried many different viruses. As a result, their polio vaccine became contaminated with a cancer-causing virus carried by these monkeys. This vaccine was given to almost 100 million people.
The virus found in this particular polio vaccine was SV40, or simian virus. It is present in human tumors, and research has established it to be a contributing factor in the rise of many types of cancer, including mesothelioma, bone, and brain cancer.
When the government became aware of this, it was downplayed for fear the public would stop accepting vaccination.

Study: Increased Risk of Noninfluenza Respiratory Virus Infections Associated With Receipt of Inactivated Influenza Vaccine

Increased Risk of Noninfluenza Respiratory Virus Infections Associated With Receipt of Inactivated Influenza Vaccine
We randomized 115 children to trivalent inactivated influenza vaccine (TIV) or placebo. Over the following 9 months, TIV recipients had an increased risk of virologically-confirmed non-influenza infections (relative risk: 4.40; 95% confidence interval: 1.31-14.8). Being protected against influenza, TIV recipients may lack temporary non-specific immunity that protected against other respiratory viruses.
Influenza vaccination is effective in preventing influenza virus infection and associated morbidity among school-aged children [1, 2]. The potential for temporary nonspecific immunity between respiratory viruses after an infection and consequent interference at the population level between epidemics of these viruses has been hypothesized, with limited empirical evidence to date, mainly from ecological studies [3–15]. We investigated the incidence of acute upper respiratory tract infections (URTIs) associated with virologically confirmed respiratory virus infections in a randomized controlled trial of influenza vaccination.

Sudden Infant Death Syndrome Rates (SIDS) Linked To Increased Vaccination Dosage

Sudden Infant Death Syndrome Rates (SIDS) Linked To Increased Vaccination Dosage

Sudden Infant Death Syndrome (SIDS)
The Thinktwice Global Vaccine Institute receives numerous emails every day. On this webpage you will find a small sample of these unsolicited personal letters linking vaccines to sudden infant death syndrome (SIDS). This webpage also includes an excerpt on SIDS from the U.S. Congressional records. We also recommend the Free SIDS Report on vaccines and Sudden Death. It includes numerous studies and other documentaion confirming a link between vaccines and infant fatalities. Be sure to read the most recent reader emails as well, which include numerous vaccine questions, comments, concerns, and unsolicited personal stories.

Special Reports

Study here:
Comparison of VAERS fetal-loss reports during three consecutive influenza seasons: Was there a synergistic fetal toxicity associated with the two-vaccine 2009/2010 season?
Abstract
The aim of this study was to compare the number of inactivated-influenza vaccine–related spontaneous abortion and stillbirth (SB) reports in the Vaccine Adverse Event Reporting System (VAERS) database during three consecutive flu seasons beginning 2008/2009 and assess the relative fetal death reports associated with the two-vaccine 2009/2010 season. The VAERS database was searched for reports of fetal demise following administration of the influenza vaccine/vaccines to pregnant women. Utilization of an independent surveillance survey and VAERS, two-source capture–recapture analysis estimated the reporting completeness in the 2009/2010 flu season. Capture–recapture demonstrated that the VAERS database captured about 13.2% of the total 1321 (95% confidence interval (CI): 815–2795) estimated reports, yielding an ascertainment-corrected rate of 590 fetal-loss reports per million pregnant women vaccinated (or 1 per 1695). The unadjusted fetal-loss report rates for the three consecutive influenza seasons beginning 2008/2009 were 6.8 (95% CI: 0.1–13.1), 77.8 (95% CI: 66.3–89.4), and 12.6 (95% CI: 7.2–18.0) cases per million pregnant women vaccinated, respectively. The observed reporting bias was too low to explain the magnitude increase in fetal-demise reporting rates in the VAERS database relative to the reported annual trends. Thus, a synergistic fetal toxicity likely resulted from the administration of both the pandemic (A-H1N1) and seasonal influenza vaccines during the 2009/2010 season

Aluminum adjuvants of vaccines injected into the muscle: Normal fate, pathology and associated disease.

Study – Aluminum adjuvants of vaccines injected into the muscle: Normal fate, pathology and associated disease.
Safety concerns largely depend on the long biopersistence time inherent to this adjuvant, which may be related to its quick withdrawal from the interstitial fluid by avid cellular uptake; and the capacity of adjuvant particles to migrate and slowly accumulate in lymphoid organs and the brain, a phenomenon documented in animal models and resulting from MCP1/CCL2-dependant translocation of adjuvant-loaded monocyte-lineage cells (Trojan horse phenomenon). These novel insights strongly suggest that serious re-evaluation of long-term aluminum adjuvant phamacokinetics and safety should be carried out.

Natural health expert and Mercola.com founder Dr. Joseph Mercola and Dr. Humphries, author of Dissolving Illusions: Disease, Vaccines, and the Forgotten History, talk about the forgotten history of vaccinations.

By Dr. Mercola
Vaccines are one of the most controversial medical therapies, and it’s impossible to make an informed decision unless you know both sides of the story. In the process of knowing both sides, the historical context is critical.

Aluminum (pronounced and spelled “aluminium” in Europe) is a known neurotoxin, and scientific evidence shows that it can play a significant role in neurological diseases, including dementia, autism, and Parkinson’s disease.
Common routes of exposure include antiperspirants, food, aluminum-based household products, and vaccines

Dr Humphries in Tampere, Finland, November 2015. Hear the arguments that pro-vaccine doctors make about aluminum (called aluminium in Europe), and the science (or lack there-of) behind it. Dr. Suzanne breaks down the issue of aluminum into fine detail to help you discuss this issue which is an Achilles heel in the vaccination argument.

Many of today’s pro-vaccine elite insist that aluminum in infant and child vaccines is totally harmless. Find out the real truth, with scientific back up. Dr Suzanne Humphries, Internist and Nephrologist, has studied out the issue and shows that Paul Offit’s absurd claim that aluminum ‘plays an important role in the development of a healthy fetus’ is completely made up. Such statements from a leading vaccine educator are flat out dangerous.
This is a clip from a 5 hour seminar on Infant Immunity from last year. The focus in this clip is aluminum. In New Zealand and Europe, aluminum is spelled and pronounced aluminium.

Hep B Vaccine Damages The Liver It Is Supposed To Protect

Hep B Vaccine Damages The Liver It Is Supposed To Protect
“According to Hippocratic tradition, the safety level of a preventive medicine must be very high, as it is aimed at protecting people against diseases that they may not contract.” ~ Marc Girard, Autoimmune hazards of hepatitis B vaccine.
Startling new research published in the journal Apoptosis indicates that hepatitis B vaccine, which is designed to prevent Hepatitis B virus-induced damage to the liver, actually causes liver cell destruction.
In the study titled “Hepatitis B vaccine induces apoptotic death in Hepa1-6 cells,” researchers set out to “…establish an in vitro model system amenable to mechanistic investigations of cytotoxicity induced by hepatitis B vaccine, and to investigate the mechanisms of vaccine-induced cell death.”1
They found the hepatitis B vaccine induced a “loss of mitochondrial integrity, apoptosis induction, and cell death” in liver cells exposed to a low dose of adjuvanted hepatitis B vaccine. The adjuvant used was aluminum hydroxide, which is increasingly being identified as a contributing cause of autoimmune disease in immunized populations.
The discovery that the hepatitis B vaccine damages the liver (hepatotoxicity) confirms earlier findings (1999) that the vaccine increases the incidence of liver problems in U.S. children less than 6 years old by up to 294% versus unvaccinated controls.
Another study published in the journal Hepatogastroentology in 2002, observed that Hepatitis B vaccination was statistically associated with gastrointestinal reactions including: hepatitis, gastrointestinal disease and liver function test abnormalities in comparison to other vaccine control groups.

Hepatitis B vaccination was statistically associated with gastrointestinal reactions including: hepatitis, gastrointestinal disease and liver function test abnormalities.

Study CONCLUSIONS:
Hepatitis B vaccination was statistically associated by chi 2 analysis with gastrointestinal reactions including: hepatitis, gastrointestinal disease and liver function test abnormalities in comparison to our vaccine control groups. The reaction rate observed is outweighed by the benefits of the vaccine. Further analysis is needed to determine the mechanisms by which hepatitis B vaccine is associated with gastrointestinal reactions.

Hepatitis B vaccine induces cell death in liver cells and mouse liver.
Study:
Vaccines can have adverse side-effects, and these are predominantly associated with the inclusion of chemical additives such as aluminum hydroxide adjuvant. The objective of this study was to establish an in vitro model system amenable to mechanistic investigations of cytotoxicity induced by hepatitis B vaccine, and to investigate the mechanisms of vaccine-induced cell death.
We conclude that exposure of Hepa1-6 cells to a low dose of adjuvanted hepatitis B vaccine leads to loss of mitochondrial integrity, apoptosis induction, and cell death, apoptosis effect was observed also in C2C12 mouse myoblast cell line after treated with low dose of vaccine (0.3, 0.1, 0.05 μg/ml). In addition In vivo apoptotic effect of hepatitis B vaccine was observed in mouse liver.

Vaccines, Retroviruses, DNA, and the Discovery That Destroyed Judy Mikovits’ Career

Vaccines, Retroviruses, DNA, and the Discovery That Destroyed Judy Mikovits’ Career
In 2011, she made the discovery that destroyed her career. She found that at least 30% of our vaccines are contaminated with gammaretroviruses. Not only is this contamination associated with autism and chronic fatigue syndrome, it is also associated with Parkinson’s, Lou Gehrig’s disease, and Alzheimer’s.
When she released this shocking information, she was warned by Dr. Andrew Wakefield that she would become a target, just as he had been. But she assured him that all of her work had been properly reviewed and, of course, she was safe.
She was wrong. She was threatened and told to destroy her data; she refused. She was fired, then arrested for supposedly stealing her data from her worksite. She had been facing charges and was bound by a gag order from the court for the last four years. Recently, charges were dropped and the gag order was lifted. Dr. Mikovits is now free to talk, and boy is she talking.
The retroviruses contaminating vaccines originate from mice used for research. Dr. Mikovits asks, “How many new retroviruses have we created through all the mouse research, the vaccine research, gene therapy research? More importantly, how many new diseases have we created?”
“When they destroyed all of our work, and discredited everything I or Frank Ruscetti had ever published, and arranged for the publication of my mug shot in Science, the NIH very deliberately sent the message to researchers everywhere about what would happen to any honest scientist who dared ask those important questions.”
New technology now exists to clean up retroviruses in vaccines and blood. Dr. Mikovits believes we will win this war, that we will eventually clean up vaccines, stop vaccinating infants, and stop injecting our children with multiple vaccines. But she also believes the government will continue to cover up their culpability in the current epidemic of autism and other diseases.
When asked about vaccine-injured children, she says, “Those are the victims. And that’s why, I’m working and why, you know, I’ll never shut up. Because they’re the victims that have been hung out to dry.”

Are fluoride levels in drinking water associated with hypothyroidism prevalence in England?

Are fluoride levels in drinking water associated with hypothyroidism prevalence in England? A large observational study of GP practice data and fluoride levels in drinking water
Findings We found that higher levels of fluoride in drinking water provide a useful contribution for predicting prevalence of hypothyroidism. We found that practices located in the West Midlands (a wholly fluoridated area) are nearly twice as likely to report high hypothyroidism prevalence in comparison to Greater Manchester (non-fluoridated area).

Researchers from the University of Kent, a public research university based in the United Kingdom, conducted the latest and considerably groundbreaking study on the health effects potentially caused by adding fluoride to the public’s water.
After studying data obtained from nearly every medical practice in England, scientists found that fluoride may be increasing the risk for hypothyroidism, or an underactive thyroid, a condition in which the thyroid gland fails to produce enough hormones, resulting in symptoms such as fatigue, obesity and depression.
Published in the Journal of Epidemiology and Community Health, the study included the largest population ever analyzed in relation to the adverse health effects caused by water fluoridation.
Recent UK study includes the “largest population ever studied in regard to adverse effects of elevated fluoride exposure”
After collecting data from 99 percent of England’s 8,020 general medical practices, researchers found that the locations with fluoridated water were 30 percent more likely to have high levels of hypothyroidism, compared to areas with low, natural levels of the chemical in the water.

Now, a report from the world’s oldest and most prestigious medical journal, The Lancet, has officially classified fluoride as a neurotoxin — in the same category as arsenic, lead and mercury.
The news was broken by author Stefan Smyle, who cited a report published in The Lancet Neurology, Volume 13, Issue 3, in the March 2014 edition, by authors Dr. Phillippe Grandjean and Philip J. Landrigan, MD. The report, which was officially released in 2014 and published in the journal, can be viewed by clicking here.

Neurodevelopmental disabilities, including autism, attention-deficit hyperactivity disorder, dyslexia, and other cognitive impairments, affect millions of children worldwide, and some diagnoses seem to be increasing in frequency. Industrial chemicals that injure the developing brain are among the known causes for this rise in prevalence. In 2006, we did a systematic review and identified five industrial chemicals as developmental neurotoxicants: lead, methylmercury, polychlorinated biphenyls, arsenic, and toluene. Since 2006, epidemiological studies have documented six additional developmental neurotoxicants—manganese, fluoride, chlorpyrifos, dichlorodiphenyltrichloroethane, tetrachloroethylene, and the polybrominated diphenyl ethers. We postulate that even more neurotoxicants remain undiscovered. To control the pandemic of developmental neurotoxicity, we propose a global prevention strategy. Untested chemicals should not be presumed to be safe to brain development, and chemicals in existing use and all new chemicals must therefore be tested for developmental neurotoxicity. To coordinate these efforts and to accelerate translation of science into prevention, we propose the urgent formation of a new international clearinghouse.

The story of the first MMR vaccine & Incidence of mumps virus meningitis

The story of the first MMR vaccine

Incidence of mumps virus meningitis:
“Vaccine-associated meningitis occurs around three weeks after immunisation generally. In those instances reported so far it appears to be a milder and more transient illness than meningitis from wild virus. This is what one might expect with an attenuated virus. The risk benefit ratio therefore remains strongly in favour of the immunisation of all children with any MMR vaccine. However the MMRII vaccine is preferred where this is available because of the much lower risk of vaccine associated meningitis.”
We have a letter from the Japanese Department of Viral Disease and Vaccine Control which indicates that from April 1993 the use of the MMR vaccine (all types) was stopped in Japan and that vaccines would be available only in their monovalent form (i.e. single virus)[21]
Comment:
The Japanese findings indicate that adverse  reactions to these types of MMR vaccine were up to  78  times as frequent as our Government’s Chief Medical Officer of Health  has admitted[22]. If those figures are correct, then the vaccine is more dangerous than the illness; and it does not give a great deal of confidence that the Government has got its figures (or information about safety or side effects) right.  Note also that this article was published in March 1991. Yet the two brands of MMR implicated with these side effects were not withdrawn until September 1992, some 18 months later.
Indeed TRIVIRIX (a MMR vaccine containing the Urabe strain virus) was withdrawn in Canada in May 1990.[23] Why did the UK Government take till 1992 to withdraw it?

Identification of chemicals that mimic transcriptional changes associated with autism, brain aging and neurodegeneration

Environmental factors, including pesticides, have been linked to autism and neurodegeneration risk using retrospective epidemiological studies. Here we sought to prospectively identify chemicals that share transcriptomic signatures with neurological disorders, by exposing mouse cortical neuron-enriched cultures to hundreds of chemicals commonly found in the environment and on food. We find that rotenone, a pesticide associated with Parkinson’s disease risk, and certain fungicides, including pyraclostrobin, trifloxystrobin, famoxadone and fenamidone, produce transcriptional changes in vitro that are similar to those seen in brain samples from humans with autism, advanced age and neurodegeneration (Alzheimer’s disease and Huntington’s disease). These chemicals stimulate free radical production and disrupt microtubules in neurons, effects that can be reduced by pretreating with a microtubule stabilizer, an antioxidant, or with sulforaphane. Our study provides an approach to prospectively identify environmental chemicals that transcriptionally mimic autism and other brain disorders

Read more at:

http://www.nature.com/ncomms/2016/160331/ncomms11173/full/ncomms11173.html

PDF:

Click to access ncomms11173.pdf