Let me start by saying, everybody acts from faith. Faith in something, no matter what it is.
A billion Catholics are not the Vatican.
The Vatican, through the Pope, has made its position clear: take the COVID vaccines.
But then there are the consciences of a billion of the faithful.
In prior articles in this series (archive here), I’ve made it clear that COVID vaccines have, in fact, relied on a fetal-tissue cell line, HEK 293, for testing, and the cell line was originally obtained via an abortion.
Moreover, the evidence points to an abortion in which the infant was delivered from her mother’s womb, alive, and then was killed by a doctor removing her kidneys for fetal tissue. Infanticide. Murder.
Does it matter whether the abortion and the murder were committed yesterday, or in a room in a hospital in the Netherlands, in 1972? Are a billion Catholics willing to say, “It was so long ago, it doesn’t have meaning anymore”?
Is that a reasonable position of Faith?
My understanding is this: Catholics believe Jesus commanded the founding of His Church, which is their Church. Does that count now? Is it wrong to contemplate what He would advise? As opposed, for example, to what Anthony Fauci would advise?
Deep sequencing reveals persistence of cell-associated mumps vaccine virus in chronic encephalitis
Abstract
Routine childhood vaccination against measles, mumps and rubella has virtually abolished virus-related morbidity and mortality. Notwithstanding this, we describe here devastating neurological complications associated with the detection of live-attenuated mumps virus Jeryl Lynn (MuVJL5) in the brain of a child who had undergone successful allogeneic transplantation for severe combined immunodeficiency (SCID). This is the first confirmed report of MuVJL5 associated with chronic encephalitis and highlights the need to exclude immunodeficient individuals from immunisation with live-attenuated vaccines. The diagnosis was only possible by deep sequencing of the brain biopsy. Sequence comparison of the vaccine batch to the MuVJL5 isolated from brain identified biased hypermutation, particularly in the matrix gene, similar to those found in measles from cases of SSPE. The findings provide unique insights into the pathogenesis of paramyxovirus brain infections
To my friends in Australia: the vaccine war deepens by Jon Rappoport
September 20, 2017
The string of abuses laid on citizens of Australia by their government grows almost week by week.
Now, parental rights to raise children, without interference from the State, is under a new form of attack. This must be resisted.
Schools are bringing doctors on board, as a permanent feature. Young children will be subjected to medical diagnoses and treatment, without consent or approval from parents, even if those parents actively object. The State is stealing the role of guardian.
The Herald Sun reports. Read carefully:
“DOCTORS will have the power to treat students as young as 12 in schools even if parents refuse their consent.”
“GPs will consult at 100 Victoria high schools for up to one day a week as part of a $43.8 million program.”
“Guidelines released on Thursday show that even if a parent ‘expressly states’ that a doctor should not [examine] their child, the GP can if they deem the teen mature enough.”
“’Any student who wants to see the GP will be permitted to make an appointment,’ the policy said.”
“The GP will decide if the young person is mature enough to provide consent to any medical treatment for the prevailing issue.”
A young child “giving consent?” This is supposed to be “informed consent” when facing off with an adult doctor?
AUSTRALIAN BABY GIRL MURDERED BY VACCINE!
Australian Medical Association: Class Action against the AMA for Vaccine Injury
Why this is important
The health and well being of our beautiful and innocent Australian children are paramount to all Australians.
It’s obvious to anyone with intelligence that there is an epidemic of ill health occurring with children around the World and particularly, with our Australian children which can be traced to Vaccine Injury through multiplying forced application of a large and growing number of untested combined vaccines riddled with known carcinogens and poisons being directly administered into the blood streams of our Australian babies and children.
Modern medical, psychological, health and nutritional sciences have grave questions as to the efficacy of these vaccines and in fact clearly, illustrate that these vaccines are in general unnecessary and poisonous and in fact interfere with the natural immune system of the human being.
We call for a moratorium of forced vaccination of Australian children and the initiation of major testing initiatives in Australia and elsewhere to prove any efficacy of injecting these poisons into our Children.
We are appalled at the support of the Australian Medical Association of these unscientific and abusive injurious procedures causing epidemic harm to our beautiful and innocent
Australian Children and demand: 1. The AMA stop all support for these appalling procedures. 2. Pay full and appropriate damages to the Australian Parents and Children injured by these AMA supported procedures. 3. Instigate a full review of these appalling procedures, based particularly on the evidence presented in the film ‘VAXXED’ and the documentation series ‘The Truth about Vaccines’, ‘Vaccines Revealed’, ‘Trace Amounts’, and ‘Vaccine Syndrome’. 4. Place the health and well‐being of our Australian children as paramount before commercial gain by Pharmaceutical and Medical industries and professionals
Deep sequencing reveals persistence of cell-associated mumps vaccine virus in chronic encephalitis
Abstract
Routine childhood vaccination against measles, mumps and rubella has virtually abolished virus-related morbidity and mortality. Notwithstanding this, we describe here devastating neurological complications associated with the detection of live-attenuated mumps virus Jeryl Lynn (MuVJL5) in the brain of a child who had undergone successful allogeneic transplantation for severe combined immunodeficiency (SCID). This is the first confirmed report of MuVJL5 associated with chronic encephalitis and highlights the need to exclude immunodeficient individuals from immunisation with live-attenuated vaccines. The diagnosis was only possible by deep sequencing of the brain biopsy. Sequence comparison of the vaccine batch to the MuVJL5 isolated from brain identified biased hypermutation, particularly in the matrix gene, similar to those found in measles from cases of SSPE. The findings provide unique insights into the pathogenesis of paramyxovirus brain infections
Tuesday, September 19, 2017
(Natural News) The Centers for Disease Control and Prevention (CDC), the same authority that determines the national vaccination schedule, notes that those most at risk of complications from the flu virus are children younger than 5, but particularly those under the age of 2; pregnant women; people in nursing homes; and adults over the age of 65. The elderly are therefore among the most vulnerable members of society when it comes to influenza. It makes sense, therefore, to believe that the flu vaccination would need to be especially effective for that demographic.
A recent report by Public Health England (PHE), however, has revealed that though it seems to have been slightly more effective at preventing influenza among children than in previous years, last year’s flu shot was totally ineffective for the elderly.
Experts believe that the shot was ineffective because it did not protect against the most common circulating strain – the H3 strain. This is because the flu shot is essentially a game of chance each year; experts have to try to predict in advance which three strains of the virus will be in circulation in the coming winter. Even in a good year, their strike rate is only 50 percent.
Of course, instead of admitting the uselessness of the vaccine, health professionals are blaming the elderly themselves.
BREAKING: Robert F. Kennedy Jr. calls for extradition of CDC vaccine criminal mastermind Poul Thorsen to face charges of criminal scientific misconduct
Thursday, September 21, 2017
(Natural News) Robert F. Kennedy Jr. (RFK Jr.) and his team at World Mercury Project have drafted up a new report that reveals the criminal conduct of CDC consultant and vaccine cultist Poul Thorsen. With an overwhelming body of evidence, RFK Jr is calling for Attorney General Jeff Sessions to take action and extradite Poul Thorsen so he can face up to his numerous crimes. In a statement, RFK Jr declared, “World Mercury Project calls upon Attorney General Jeff Sessions to extradite Thorsen back to the U.S. to face prosecution. We also call upon Secretary of Health and Human Services Dr. Tom Price to retract the Thorsen-affiliated autism research papers that are the fruit of illegally conducted research.”
What has World Mercury Project (WMP) uncovered? In addition to evidence of criminal activity, new findings by WMP show that Thorsen and his team never obtained permission from the Institutional Review Board (IRB) to do their studies, published in 2002 by the New England Journal of Medicine and in 2003 by the journal Pediatrics. As WMP explains, this alone detracts from the validity of their research, but to make matters worse, records indicate that the CDC was complicit in covering up this little “mistake.” According to the WMP report, CDC staff realized that no IRB approval had ever been granted for Thorsen’s research, but the error was simply ignored and the studies were never retracted. Freedom of Information Act documents show that supervisors at the CDC looked the other way and actively tried to conceal what transpired.
Criminal Conduct – Poul Thorsen
Robert F. Kennedy, Jr. and World Mercury Project Issue Report Regarding New Evidence of Ongoing Corruption and Scientific Misconduct at CDC
Kennedy hopes new evidence and a fresh look at criminal misconduct will result in law enforcement action, rigorous and transparent vaccine safety science, and safer vaccines.
In a new report released September 18, 2017, Robert F. Kennedy, Jr. and his team outlined various criminal acts on the part of employees and consultants for the Centers for Disease Control and Prevention (CDC) whose questionable ethics and scientific fraud have resulted in untrustworthy vaccine safety science.
HighWire with Del Bigtree – Jimmy Kimmel the Hypocrite. Vaccine Risk Now Mainstream!
One vaccine injection could carry many doses
Microparticles created by new 3-D fabrication method could release drugs or vaccines long after injection.
Anne Trafton | MIT News Office
September 14, 2017
MIT engineers have invented a new 3-D fabrication method that can generate a novel type of drug-carrying particle that could allow multiple doses of a drug or vaccine to be delivered over an extended time period with just one injection.
The new microparticles resemble tiny coffee cups that can be filled with a drug or vaccine and then sealed with a lid. The particles are made of a biocompatible, FDA-approved polymer that can be designed to degrade at specific times, spilling out the contents of the “cup.”
“We are very excited about this work because, for the first time, we can create a library of tiny, encased vaccine particles, each programmed to release at a precise, predictable time, so that people could potentially receive a single injection that, in effect, would have multiple boosters already built into it. This could have a significant impact on patients everywhere, especially in the developing world where patient compliance is particularly poor,” says Robert Langer, the David H. Koch Institute Professor at MIT.
Langer and Ana Jaklenec, a research scientist at MIT’s Koch Institute for Integrative Cancer Research, are the senior authors of the paper, which appears online in Science on Sept. 14. The paper’s lead authors are postdoc Kevin McHugh and former postdoc Thanh D. Nguyen, now an assistant professor of mechanical engineering at the University of Connecticut.
A legal process has been initiated for a 5 year moratorium on childhood vaccines until tests can be conducted. This is not merely an internet petition, or a White House petition (although one has been started) but the beginning of a basis to take legal action — and we have a sympathetic ear in President Trump.
Full video to share with those not on Facebook – youtube.com/watch?v=rjGKqPoaS_w #VaccineMoratorium #RevolutionForChoice #InformedConsent #Vaxxed #HearThisWell
Vaxxed – A Revolution For Choice
How will it end? What pivotal event will historians point to and say that was the day the madness ended? I think I know.
This is a studio version of a talk I gave at the CDCTruth event in Atlanta on October 15, 2016.
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237 deaths by Pentavalent vaccine and still counting
By JACOB PULIYEL | NEW DELHI | 13 November, 2016
Under Right to Information we know that up to August 2016 there have been 237 deaths reported to the government here within 72 hours of vaccination with Pentavalent. We examined deaths in states which were giving DPT and Pentavalent vaccine concurrently.
There were three deaths following the use of Pentavalent vaccine in Sri Lanka. The Government of Sri Lanka suspended the use of the vaccine. WHO experts investigated the deaths. They found there was a clear temporal association of the deaths to the vaccine (WHO terminology, meaning the deaths followed soon after vaccination) and there was no alternate explanation for the deaths. According to the standard protocol in investigation of vaccine deaths these deaths would have to be declared as “probably” caused by Pentavalent vaccine. The experts balked at the prospect of giving such a report. No country would use this vaccine after that. Instead they wrote in their report that they were deleting “probable” and “possible” from the standard classification. The report maintained that although it was probably related to vaccine, they were reporting it as “unlikely” to be related to vaccination.
The full report was not published online, only the conclusion was made public.
The full report was presented to the Delhi High Court in a vaccine case. Once this devious methodology employed by the WHO experts was known, it was exposed by the British Medical Journal.
Following the exposé, the WHO set up a 40-member committee called the CIOMS/WHO committee. 19 of the 40 were representatives of vaccine manufacturers with conflicts of interest. They developed a new algorithm for investigating adverse events after immunization, which decreed that any reaction seen first in Phase 4 trial must be ignored.
When a drug is developed it is tested in a randomised controlled trial called the Phase 3 trial. The numbers tested are limited to a few thousand. If there is no adverse reaction the drug is licensed for Phase 4 trials with it given to a larger number. Reactions that happen less than 1 in 10,000 are noticed for the first time in Phase 4 trials. If the same reaction happens repeatedly it is considered as a “signal” that the reaction is caused by the drug and studies in the community in the form of case-control investigations are done to establish if the reactions happen in the community setting.
But here are the important questions regarding HPV:
If two doses are just as effective as three, why recommend three doses in the first place, especially for a vaccine that costs $120 per dose (the highest of the childhood vaccine schedule)? And would they have discovered this error if they had completed the full four years of safety/efficacy research instead of fast-tracking the vaccine? The new schedule recommends 6 to 12 months between the two doses. Are they increasing the time between doses to reduce the number of severe neurological reactions? Couldn’t they have discovered that if they had stuck to the four-year safety study? And more concerning, could this also be true for other vaccines?
Asking questions about whether or not vaccines are truly “safe and effective” doesn’t make you anti-vaccine. You have the right to know.
In an unprecedented move last November, the CDC announced they were reducing the number of doses of recommended HPV vaccine from 3 doses to 2 AND warning doctors to wait longer before giving the second dose. The 3-dose series has been the existing recommendation for nearly a decade, and on the current CDC schedule, which advises 70 doses of vaccines for all children, the HPV vaccine is recommended for all boys and girls 11 to 18 years old.
They say the reduced recommendation is to gain better compliance, but the reality is the CDC may have been overdosing American teens by putting the first two doses too close together, triggering severe neurological and autoimmune reactions. Research has shown that most severe side effects occurred after that second dose (given only 1 month after the first). And now the CDC has found that three doses, which they had been advising for 10 years, has no better efficacy – only more side effects. Isn’t this information something that should have been discovered during initial safety testing? And is there a chance there are unnecessary doses of other vaccines on the CDC schedule that may be causing more harm with no actual benefit?
Eyes wide open yet?
This is a 3 yr. Old little boy who is having a severe reaction to the chicken pox vaccine..
He was diagnosed yesterday and the Dr. states in his discharge papers that it was caused by the vaccine. This is his 2nd reaction to a vaccine. The symptom is the blisters that you see, and are very painful and itchy. He is attending an independent private school and apparently this is required..
Do we not see something severely wrong here??
CANCER IN KIDS?!!
Cancer is now the 2nd leading cause of DEATH in children.
Remember when it used to mostly affect older people. What’s going on here?
Could it be that most VACCINES contain a toxic additive called Formaldehyde that is KNOWN to cause cancer in humans when you inhale it?
Pharmaceutical companies would like you to think that when you inject it, it magically becomes “safe”. It is not safe in any amount and when injected, it’s far more potent than when inhaled. Pharma thinks we are stupid enough to believe in magic…but you are not falling for that lie, right?!!
NOT A COINCIDENCE! #LearnTheRIsk #cancer #askWHY
Vaccine injury
13 Year-Old Boy Permanently Disabled from Chicken Pox Vaccine Wins His Case in Vaccine Court
A young man was recently awarded compensation in the United States Court of Federal Claims Vaccine Court, for injuries he sustained after being administered the hepatitis A and varicella vaccinations in 2009. After five long years of litigation, Health and Human Services (HHS), the Respondent in all vaccine injury cases, conceded that the varicella vaccination did in fact cause RD’s vaccine injury, transverse myelitis, which has left him a tetraplegic.
In November 2014, HHS conceded that the vaccination caused RD’s injuries. Even with this concession, his case continued for another year in the damages phase, during which time the parties continued to negotiate the amount of damages that RD would receive for his injuries. Although he was compensated for his suffering and injuries, the monetary award will never compensate for the lifelong effects this young man is suffering from his vaccine injury.
Five Long Years
RD was only 13 when his life changed forever. At a routine well-child visit in 2009, the doctor informed RD’s parents that he was due to receive the hepatitis A and varicella vaccinations. His parents complied with the doctor’s order and RD received the vaccinations.
RD’s mother explained that, at that time in RD’s state, only one dose of varicella vaccine was required and RD had already received one dose of that vaccine. This second dose that was administered to RD at this well visit was determined to be the cause of RD’s horrific injuries, and it was not even required for him, which his family didn’t realize until it was too late.
About 14 days later, RD began to experience excruciating pain shooting through his body along with tingling, numbness and paralysis of his limbs. After extensive testing and many invasive procedures, RD was diagnosed with transverse myelitis.
Breaking: interview with Vaxxed producer who was banned from Australia
Producer of film Vaxxed banned from Australia
by Jon Rappoport
August 9, 2017
Polly Tommey, producer of the famous documentary, Vaxxed (trailer), has been banned from Australia. If that sounds quite insane—it is.
Vaxxed has been screening across the world. It is an explosive revelation about egregious fraud at the US Centers for Disease Control (CDC).
The film focuses on the 2014 public confession of a long-time researcher at the CDC, William Thompson. Thompson admits that he and his colleagues committed a crime, by manipulating data to give the MMR vaccine a free pass, “proving” it had no connection to autism—when in fact, as Thompson states, the vaccine does raise the risk of autism in children.
Here are a few statements from the The Sydney Morning Herald’s report, headlined: “Anti-vaccination advocate ‘banned from Australia’ after documentary tour.”
“The producer Polly Tommey behind a controversial anti-vaccination film which has been touring Australia has been banned from returning to the country for three years, she claims.”
“Ms Tommey spearheaded a sold-out national roadshow of the documentary Vaxxed: From Cover-up to Catastrophe organised by the Australian Vaccinations-Skeptics Network.”
“In a video, posted to Youtube on Tuesday, Ms Tommey claimed authorities seized her phone and copied her emails as she left Australian soil to continue the New Zealand leg of the film tour.”
Educate before you vaccinate!!! tiny.cc/FreeVaccinationEducation
More information on glyphosate in vaccines: ecowatch.com/glyphosate-vaccines-1999343362.html Jeffrey M. Smith is the director of the Institute for Responsible Technology and is one of the world’s leading advocates against GM foods. His book Seeds of Deception is rated the number one book on the subject and has had a substantial influence on public perception and even legislation. Smith has reached tens of millions of people through hundreds of media interviews. He produced the video Hidden Dangers in Kids’ Meals, and also writes a popular monthly syndicated column. He is on the Genetic Engineering Committee of the Sierra Club, was the former vice president of marketing for a GMO detection laboratory, and ran for U.S. Congress in his home state of Iowa to raise public awareness of the health and environmental dangers of GM foods.
Find his books here: amazon.com/Jeffrey-M.-Smith/e/B001JRXVHC/ref=ntt_dp_epwbk_0
Networking, exemption information and doctor resources: tinyurl.com/RevolutionForVaccineChoice
Follow us: facebook.com/RevolutionForChoice
Read all vaccine inserts: tinyurl.com/ReadTheVaccineInsert #RevolutionForChoice #InformedConsent #Monsanto #Pesticides #Glyphosate #EducateBeforeYouVaccinate #VAXXED
“…what we’re told to do.” Full Interview:
Editor: Robin Aris
Air Pollution Linked To Measles Incidence, Proving Immune Status Is Vital In Disease Risk
Posted on: Sunday, May 14th 2017 at 5:45 am
Written By: Sayer Ji, Founder
The idea that measles virus is solely responsible for causing measles infection, and that vaccination alone is the way to prevent it, has been undermined by a new Chinese air pollution study.
A new study published in the journal Environmental Research reveals that exposure to air pollution is significantly associated with measles incidence in China. This is consistent with the view that infection is not solely determined by exposure to a virus particle but also involves the immune status of the subject which depends on various nutritional and environmental factors, including the immunosuppressive function of air pollution. In other words, it’s not just the “germ” alone but the terrain that determines disease.
In the new study titled, “Is short-term exposure to ambient fine particles associated with measles incidence in China? A multi-city study,” Chinese researchers examined the relationship between short-term exposure to ambient particles with a diameter of less than ≤2.5µm (i.e. 2.5 microns thick) and measles incidence in China. They noted that rapid economic development has resulted in “severe particulate matter (PM) air pollution.”
Their method was to collect data on the daily number of new measles cases and concentrations of ambient particles (≤2.5µm) from 21 cities in China between October 2013 and December 2014 and to analyze data to ascertain the effects at the national scale.
Study – Is short-term exposure to ambient fine particles associated with measles incidence in China? A multi-city study.
RESULTS:
A 10µg/m3 increase in PM2.5 at lag 1day, lag 2day and lag 3day was significantly associated with increased measles incidence [relative risk (RR) and 95% confidence interval (CI) were 1.010 (1.003, 1.018), 1.010 (1.003, 1.016) and 1.006 (1.000, 1.012), respectively]. The cumulative relative risk of measles associated with PM2.5 at lag 1-3 days was 1.029 (95% CI: 1.010, 1.048). Stratified analyses by meteorological factors showed that the PM2.5 and measles associations were stronger on days with high temperature, low humidity, and high wind speed.
CONCLUSIONS:
We provide new evidence that measles incidence is associated with exposure to ambient PM2.5 in China. Effective policies to reduce air pollution may also reduce measles incidence.
Nursing Student Dismissed for Refusal to Lie about Vaccines Wins Early Court Victory
By Paul Webber – June 5, 2017
“Nurses Need to Obey the Patient’s Directives, Not Threaten or Lie”
Nurse is dismissed from Baker College in Michigan for questioning vaccines
The nurse files suit against Baker College
Baker College attempts to dismiss the case; Judge denies request
Michigan law protects patient rights
Back in 2013, nursing student Nichole Rolfe, claims she was asked by her Baker college instructors to threaten patients who opted to not vaccinate. The threats included ‘giving them false information’ and even ‘withholding state medical assistance’ to those who questioned whether or not they’d vaccinated. Last week, a judge declined Baker college’s request to dismiss the suit and prevents any severe alterations to the suit. According to olcplc.com, Michigan patients most certainly do have the right to choose (and without intimidation).
Study – Vaccines for measles, mumps and rubella in children
MAIN RESULTS:
We included five randomised controlled trials (RCTs), one controlled clinical trial (CCT), 27 cohort studies, 17 case-control studies, five time-series trials, one case cross-over trial, two ecological studies, six self controlled case series studies involving in all about 14,700,000 children and assessing effectiveness and safety of MMR vaccine. Based on the available evidence, one MMR vaccine dose is at least 95% effective in preventing clinical measles and 92% effective in preventing secondary cases among household contacts.Effectiveness of at least one dose of MMR in preventing clinical mumps in children is estimated to be between 69% and 81% for the vaccine prepared with Jeryl Lynn mumps strain and between 70% and 75% for the vaccine containing the Urabe strain. Vaccination with MMR containing the Urabe strain has demonstrated to be 73% effective in preventing secondary mumps cases. Effectiveness of Jeryl Lynn containing MMR in preventing laboratory-confirmed mumps cases in children and adolescents was estimated to be between 64% to 66% for one dose and 83% to 88% for two vaccine doses. We did not identify any studies assessing the effectiveness of MMR in preventing rubella.The highest risk of association with aseptic meningitis was observed within the third week after immunisation with Urabe-containing MMR (risk ratio (RR) 14.28; 95% confidence interval (CI) from 7.93 to 25.71) and within the third (RR 22.5; 95% CI 11.8 to 42.9) or fifth (RR 15.6; 95% CI 10.3 to 24.2) weeks after immunisation with the vaccine prepared with the Leningrad-Zagreb strain. A significant risk of association with febrile seizures and MMR exposure during the two previous weeks (RR 1.10; 95% CI 1.05 to 1.15) was assessed in one large person-time cohort study involving 537,171 children aged between three months and five year of age. Increased risk of febrile seizure has also been observed in children aged between 12 to 23 months (relative incidence (RI) 4.09; 95% CI 3.1 to 5.33) and children aged 12 to 35 months (RI 5.68; 95% CI 2.31 to 13.97) within six to 11 days after exposure to MMR vaccine. An increased risk of thrombocytopenic purpura within six weeks after MMR immunisation in children aged 12 to 23 months was assessed in one case-control study (RR 6.3; 95% CI 1.3 to 30.1) and in one small self controlled case series (incidence rate ratio (IRR) 5.38; 95% CI 2.72 to 10.62). Increased risk of thrombocytopenic purpura within six weeks after MMR exposure was also assessed in one other case-control study involving 2311 children and adolescents between one month and 18 years (odds ratio (OR) 2.4; 95% CI 1.2 to 4.7). Exposure to the MMR vaccine was unlikely to be associated with autism, asthma, leukaemia, hay fever, type 1 diabetes, gait disturbance, Crohn’s disease, demyelinating diseases, bacterial or viral infections.
AUTHORS’ CONCLUSIONS:
The design and reporting of safety outcomes in MMR vaccine studies, both pre- and post-marketing, are largely inadequate. The evidence of adverse events following immunisation with the MMR vaccine cannot be separated from its role in preventing the target diseases.
Fluzone contains:
Formaldehyde: A chemical usually used in building materials, as well as industrial fungicide. In medical laboratories, it is used as a preservative. Long-term effects have not been fully studied, as the National Cancer Institute admits. A study of funeral industry workers found a link between formaldehyde and myeloid lukemia, and professionals such as anatomists and embalmers reported increased risks of leukemia and brain cancer when working with formaldehyde.
Octylphenol ethoxylate (Triton X-100): is a product created by a few chemical companies including DOW. It is used for “wetting, detergency, superior hard surface, metal cleaning and excellent emulsification” in paints, coatings, oilfield chemicals, textiles, and industrial cleaners. In 1995 an article raised a question if this chemical is toxic to the reproductive system. In the fact sheet for Triton, the chemical is listed as possibly toxic to specifically the female reproductive system, and mutagenic for mammalian somatic cells (may change DNA of skin, bones, blood and connective tissue cells.
Thimerosal (standard dosage multi-dose vial): is a mercury-based preservative used in flu shots and some childhood vaccines. The ingredient has caused a lot of controversy since 1990s. It is a neurotoxin; it can cause nerve damage, and FDA knows of numerous cases of mercury poisoning caused by thimerosal.
Other ingredients in Fluzone are: sodium phosphate-buffered isotonic sodium chloride solution and gelatin
Read more about Fluzone reactions here : More Than 100 Seniors Died After Receiving This Flu Shot Given By Pharmacies
by Yelena Sukhoterina | January 6, 2016
As it happens every winter, the marketing push for receiving a flu shot continues. CVS is offering a 20% shopping pass when you get your flu shot. They are also marketing a high-dose vaccine, which is of course more profitable for the manufacturer and the pharmacy, but there are plenty of reasons to be wary of it — especially for seniors.
Fluzone® High-Dose is an injectable vaccine, specifically approved for people ages 65 and older. Manufactured by Sanofi Pasteur, this shot contains three flu strains and four times more antigen (substance that causes an immune response) than regular flu shots, claims CVS Pharmacy (Rite Aid also offers it and admits that “more studies are being done” to see whether it actually offers an improvement at all).
The pharmacy does admit that the vaccine is not recommended for anyone who has experienced an adverse reaction (especially Guillain-Barré syndrome) to vaccines in the past.
But between their marketing campaigns and promoting a 20% shopping coupon, they omitted a vital piece of information: 105 seniors died after taking part in two Fluzone high-dose vaccine trials, and 91 died after getting the regular Fluzone vaccine.
Vaccines contain many toxic ingredients, but they vary by manufacturer.
Other flu shots are made from different potentially toxic ingredients:
Afluria (Trivalent) contains:
Monobasic sodium phosphate (MSP): when used in high doses during colon cleansing, it has caused acute phosphate nephropathy, and permanent impairment of renal functions. It has also caused seizures, and cardiac arrhythmias.
Dibasic sodium phosphate and monobasic potassium phosphate: Phosphates are often used in food as preservatives, acidifying, and emulsifying agents. German researchers concluded that it is “damaging to health,” especially to the renal function, and is linked to cardiovascular and overall mortality.
Potassium chloride: has been most commonly linked to digestive problems and vomiting, but in severe cases it can lead to severe allergic reactions, chest pains, irregular heartbeat, confusion, and paralysis.
Calcium chloride: may lead to cardiovascular issues.
Sodium taurodeoxycholate: have been associated to promote tumor growth, particularly in pancreas, colon, and throat, studies show.
Neomycin sulfate: in rare cases has been linked to drowsiness, loss of hearing, difficulty breathing, rash, and weakness.
Polymyxin B: is an antibiotic, whose side effects include neurotoxic and nephrotoxic reactions: rising blood levels, dizziness, apnea, fever, and headache.
Mercury: a heavy metal responsible for poisoning, and damage to many organs leading to severe illnesses, including severe insomnia, and neurological disorders.
Beta-propiolactone is a carcinogen and a possible toxin to liver, skin, respiratory tract, and gastrointestinal tract.
Aluminum Should Now Be Considered a Primary Etiological Factor in Alzheimer’s Disease
Abstract
In this paper, I have summarized the experimental and largely clinical evidence that implicates aluminum as a primary etiological factor in Alzheimer’s disease. The unequivocal neurotoxicity of aluminum must mean that when brain burdens of aluminum exceed toxic thresholds that it is inevitable that aluminum contributes toward disease. Aluminum acts as a catalyst for an earlier onset of Alzheimer’s disease in individuals with or without concomitant predispositions, genetic or otherwise. Alzheimer’s disease is not an inevitable consequence of aging in the absence of a brain burden of aluminum.
EVIDENCE NOW POINTS TO ALUMINUM AS A CONTRIBUTORY FACTOR IN ALL FORMS OF ALZHEIMER’S DISEASE
Aluminum is unquestionably neurotoxic [1] and it is accepted as the cause of encephalopathies in, for example, individuals undergoing renal dialysis [2] and similarly in individuals who have received aluminum-based prostheses [3]. There are myriad ways by which aluminum can exert toxicity; its Al3 + (aq) ion is highly biologically reactive, but to do so and thereby bring about change in a biochemical system, the aluminum content of any compartment, such as a tissue, must achieve a toxic threshold or burden [4]. However, aluminum-induced encephalopathies are not Alzheimer’s disease, though they may share some similar neuropathological hallmarks [5]; they are acute conditions whereas Alzheimer’s disease might now be considered as an acute response to chronic intoxication byaluminum [1].
Shocker: study unwittingly links vaccines to autism
Jun 14 2017
by Jon Rappoport
A new study links fever in pregnant women to an increased risk of autism in their babies.
MedicalNewsToday (6/13/17): “A study of a large group of children found a link between raised risk of autism spectrum disorder and their mothers reporting fever during pregnancy. The link was strongest with fevers reported during the second trimester.”
“The study – led by the Mailman School of Public Health at Columbia University in New York City, NY – also found that the risk of autism increased in line with the number of fevers reported after 12 weeks of gestation – rising to 300 percent higher risk [of autism] with reports of three or more fevers.”
Next, here is a one-word item from the World Health Organization web page, Vaccine Safety Basics. The item comes under the heading of “minor vaccine reactions,” and applies to every vaccine: the reaction is FEVER.
Pregnant woman gets vaccines. Vaccines cause fevers. Fevers are linked to autistic babies.
Here is a CDC list of vaccines given to pregnant women, under various conditions: HepA, HepB, Flu, Tdap (tetanus, diphtheria, pertussis), meningococcal, polio, Rabies. Fever, as a typical and minor adverse effect, would be expected and ignored for ANY AND ALL of these vaccines.
Accepting the finding of the new study, cited above—routine vaccination for pregnant women is linked to an increased risk of autism in their babies.
That’s it in a nutshell.
Fever in pregnancy tied to higher risk of autism
By Catharine Paddock PhD
published Tuesday 13 June 2017
The risk of developing autism spectrum disorder is stronger among children whose mothers experienced fever during pregnancy.
A study of a large group of children found a link between raised risk of autism spectrum disorder and their mothers reporting fever during pregnancy. The link was strongest with fevers reported during the second trimester.
The study – led by the Mailman School of Public Health at Columbia University in New York City, NY – also found that the risk of autism increased in line with the number of fevers reported after 12 weeks of gestation – rising to 300 percent higher risk with reports of three or more fevers.
In the journal Molecular Psychiatry, the researchers say that their findings support the idea that infection in pregnancy – and the way in which the immune system responds to it – may play a role in the development of some cases of autism.
Prenatal fever and autism risk
Abstract
Some studies suggest that prenatal infection increases risk of autism spectrum disorders (ASDs). This study was undertaken in a prospective cohort in Norway to examine whether we could find evidence to support an association of the prenatal occurrence of fever, a common manifestation of infection, with ASD risk. Prospective questionnaires provided maternal exposure data; case status was established from clinical assessments and registry linkages. In a large, prospectively ascertained cohort of pregnant mothers and their offspring, we examined infants born greater than or equal to32 weeks for associations between fever exposure in each trimester and ASD risk using logistic regression. Maternal exposure to second-trimester fever was associated with increased ASD risk, adjusting for presence of fever in other trimesters and confounders (adjusted odds ratio (aOR), 1.40; 95% confidence interval, 1.09–1.79), with a similar, but nonsignificant, point estimate in the first trimester. Risk increased markedly with exposure to three or more fever episodes after 12 weeks’ gestation (aOR, 3.12; 1.28–7.63). ASD risk appears to increase with maternal fever, particularly in the second trimester. Risk magnified dose dependently with exposure to multiple fevers after 12 weeks’ gestation. Our findings support a role for gestational maternal infection and innate immune responses to infection in the pathogenesis of at least some cases of ASD.
Vaccine injury testimony
Monsanto Admits Injecting Glyphosate a Hazard – Too Bad It’s In Vaccines
Tue 9:30 am UTC, 13 Jun 2017
posted by Gordon
Monsanto Toxicologist Donna Farmer recently made the following statement regarding the toxicity of Glyphosate:
“I’ll give you an example of one of the studies,” she said during the debate, which was aired as part of The Doctors, an award-winning TV show. “They actually injected the Round-Up formulation into the abdomen of the animals and they did have an effect. But that’s not a relevant route of exposure for somebody who is going to be spraying that herbicide. So that’s what we look at and the regulatory agencies look at and, like the other bodies at the World Health Organization. IARC only looks and says, “If I inject it there’s a hazard.” So there’s different ways we look at the data.”
Interestingly enough, Glyphosate is a known vaccine contaminant in vaccines deemed “acceptable” by the FDA.
This list of vaccine ingredients indicates the culture media used in the production of common vaccines and the excipients they contain. Most vaccines listed are produced on cultures containing either egg, which are allowed to contain 0.05 mg/Kg glyphosate residues, or Bovine serum albumin, which are from cows allowed to eat fodder that contain 500 mg/Kg glyphosate residues. Also listed are substances used in the manufacturing process.
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