Vaccine News – Are you sure you can trust these untouchable corporate entities to manufacture the vaccines injected into your beloved children?

The Richie Allen Show – Toni Bark MD “Evidence Is Emerging That Vaccine Safety Studies Are Being Rigged By Pharma!”
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The Richie Allen Show – Rima E. Laibow: “Vaccines Are A Complete Fraud. Don’t Poison Your Child!”

Dr Toni Bark on Gardasil
This is the Vaccine Panel that was held on February 20, 2016 in Los Angeles at the Conscious Life Expo. The panel is moderated by Kelly Gallagher and the speakers include Dr. Andrew Wakefield M.D., Dr. Toni Bark, Karen Kain, Brandy Vaughan, Allison Jones, Wendy Silvers, Larry Cook and Dr. Nick Delgado. The discussion includes everything vaccine related including a Q&A from the audience. The panel was produced by Dawna Shuman B-roll camera by Jesus Curioso. Camera and editing by Joshua Coleman.
To watch the entire clip, click here: https://www.youtube.com/watch?v=F8uradn98Ls

VAXXED TV – Dr. Suzanne Humphries on Gardasil
Dr. Suzanne Humphries and Polly Tommey go through the Gardasil inserts and explore how the safety and efficacy research was done and what the results were. Camera by Joshua Coleman and Anu Vaidya with editing by Joshua Coleman.

VAXXED TV – VaxXed Tour: Forrest and Dr. Suzanne on Herd Immunity
Forrest Maready and Dr. Suzanne Humphries discuss the idea of “herd immunity” and how, when applied to vaccination, the concept is flawed.
#RFKcommission #VaxXed
Interview by Polly Tommey and camera by Joshua Coleman

Dr. Mercola and Barbara Loe Fisher – Herd Immunity
Natural health physician and Mercola.com founder Dr. Joseph Mercola and Barbara Loe Fisher discuss herd immunity specifically relates to pertussis.
http://articles.mercola.com/sites/articles/archive/2011/11/01/more-parents-waking-up-to-vaccine-dangers.aspx

The Richie Allen Show – Dr Judy Mikovits “We Are Carrying Potentially Deadly Retroviruses We Acquired Through Vaccination!”

Dr Judy – Truth Revealer – Vaccine Injury
Please re-post. Vaccine injury, Cancers, Alzheimers, Auto immune diseases, Allergies, Chronic fatigue syndrome, genocide, corporate deception

Vaccination: The Hidden Truth (1998)
This program was produced in Australia and features contributions from medical doctors, authors, researchers, and victims. If you have small children in your family, you owe it to them to become aware of these facts.
In this extremely informative video, fifteen people, including Dr. Viera Scheibner (a PhD researcher), five medical doctors, other researchers, reveal what is really going on in relation to illness and vaccines. Ironically, the important facts come from the orthodox medicine’s own peer-reviewed research.
The video presents well documented answers to questions like: Was it really vaccines that saved us? Why are they only counterproductive? How are many statistics misleading? What do vaccines contain? What are they doing to our organs, immune systems, even our genes? Are childhood diseases really dangerous to healthy children? Why does vaccination continue? What are our rights? Can vaccine damage be evaluated and countered? What is the true key to immunity?
With so much government and medical promotion of vaccination for prevention of disease, the video is clearly devoted to presenting the other side of the issue that parents and others are not being told. The result is a damning account of the ineffectiveness of vaccines and their often harmful effects. It declares that parents are not being told the truth by the media, the Health Department and the medical establishment, with a medical doctor, Dr. Mark Donohoe, confessing that “It is a problem for me that I am part of a profession that is systematically lying to people…”
Do vaccinations cause more childhood diseases than they prevent?
FAIR USE
I believe this constitutes a ‘fair use’ of any such copyrighted material as provided for in section 107 of the US Copyright Law. In accordance with Title 17 U.S.C. Section 107, the material on this channel is distributed without profit to those who have expressed a prior interest in receiving the included information for research and educational purposes.

The Richie Allen Show – Graham Downing “Through Vaccines & Statins Big Pharma Is Engaged In All Out Assault On Our Health!”

The Indegraph Times – Health Epidemics & The Untold Story of Vaccines

Jeff Sessions: 400 medical professionals charged in largest health care fraud takedown
Kevin Johnson , USA TODAY Published 9:55 a.m. ET July 13, 2017 | Updated 2:35 p.m. ET July 13, 2017
Attorney General Jeff Sessions and Health and Human Services Secretary Tom Price announced what they called the largest-ever health care fraud takedown in American history
WASHINGTON – Federal authorities announced charges Thursday against 412 physicians, nurses, pharmacists and other medical professionals, in what Attorney General Jeff Sessions called the largest health care fraud enforcement operation in U.S. history.
Sessions said the suspects accounted for more than $1.3 billion in fraudulent transactions across more than 20 states, and at least 120 people were charged for their alleged roles in overprescribing and distributing opioids, making it also the largest-ever opioid-related fraud takedown.
Of the 412 charged in the year-long operation, 56 were physicians.
“Too many trusted medical professionals…have chosen to violate their oaths and put greed ahead of their patients,” Sessions said. “Amazingly, some have made their practices into multi-million dollar criminal enterprises.”

Dr. Jayne Donegan, British GP, who wrote the foreword to Dissolving Illusions tells how she went 180 degrees on vaccines in the course of her medical career. She won her case when the GMC tried to shut her down and accuse her of “serious medical misconduct”. #vaxxed #truth #science #PrayBig

Are you sure you can trust these untouchable corporate entities to manufacture the vaccines injected into your beloved children? Learn all you can, while this life-changing series is still playing for free >>> tinyurl.com/9Episodes
✴️ Networking, exemption information and doctor resources: tinyurl.com/RevolutionForVaccineChoice
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#RevolutionForChoice #InformedConsent #EducateBeforeYouVaccinate #VAXXED #BigPharma #VaccineInjury #HearThisWell

This week’s Scream of the Week: Another vaccine developed for pregnant women…with an additional load of injected aluminum.
https://vaccineresearchlibrary.com/scream-206-rsv-vaccine-in-phase-2-trials-in-women-of-childbearing-age/

Dr. Wakefield on the coordinated and concerted efforts to bury the real science, skew the studies and demoralize the whistle-blowers and truth-tellers, by those with a #ConflictOfInterest!
Networking, resources and much needed group support is here: tinyurl.com/RevolutionForVaccineChoice
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READ ALL VACCINE INSERTS: facebook.com/notes/vaxxed-a-revolution-for-choice/reading-the-vaccine-insert-is-the-first-step-towards-informed-consent/185106191896975
#MMR #RevolutionForChoice #InformedConsent #EducateBeforeYouVaccinate #VAXXED #BoughtByPharma

Mercury and Autism Relationship Confirmed in Longitudinal Study
July 12, 2017
By Robert F. Kennedy, Jr.
The international journal Science of the Total Environment has just published a compelling study from the Republic of Korea, where autism prevalence is high. The study identifies a strong relationship between prenatal and early childhood exposure to mercury and autistic behaviors in five-year-olds.
Lead author Jia Ryu and coauthors acknowledge mercury’s potential for neurotoxicity straight away but choose to characterize previous findings on the mercury-autism relationship as “inconsistent.” They attribute the seeming lack of consistency, in part, to methodological issues, especially flagging problematic cross-sectional study designs that measure autistic behaviors and mercury levels (in either blood or hair) at a single point in time. To rectify these methodological weaknesses, Ryu and coauthors report on data from a multi-region longitudinal study in the Republic of Korea called the Mothers and Children’s Environmental Health (MOCEH) study.
The ongoing MOCEH study examines environmental exposures during pregnancy and childhood and their effects on children’s growth and development. A unique feature is that it includes five different blood samples: maternal blood from early and late pregnancy; cord blood; and samples from children at two and three years of age. In addition, the study asks mothers to complete three follow-up surveys and—when their child reaches age five—the 65-item Social Responsiveness Scale (SRS), which assesses autistic behaviors.

Study – Associations of prenatal and early childhood mercury exposure with autistic behaviors at 5 years of age: The Mothers and Children’s Environmental Health (MOCEH)
Highlights
•We explored the associations between blood mercury levels and autistic behaviors.
•This study involved an ongoing multi-center prospective birth cohort.
•Blood mercury levels were repeatedly measured from early pregnancy to 3 years.
•Autistic behaviors were assessed at 5 years with the Social Responsiveness Scale.
•Prenatal and early childhood mercury levels were associated with autistic behaviors.
Results
The geometric mean of mercury concentrations in cord blood was 5.52 μg/L. In adjusted models, a doubling of blood mercury levels at late pregnancy (β = 1.84, 95% confidence interval [CI]: 0.39, 3.29), in cord blood (β = 2.24, 95% CI: 0.22, 4.27), and at 2 years (β = 2.12, 95% CI: 0.54, 3.70) and 3 years (β = 2.80, 95% CI: 0.89, 4.72) of age was positively associated with the SRS T-scores. When the SRS T-scores were dichotomized, we observed positive associations with mercury levels at late pregnancy (relative risk [RR] = 1.31, 95% CI: 1.08, 1.60) and in cord blood (RR = 1.28, 95% CI: 1.01, 1.63).
Conclusion
We found that blood mercury levels at late pregnancy and early childhood were associated with more autistic behaviors in children at 5 years of age. Further study on the long-term effects of mercury exposure is recommended.

Study – Prevalence of Autism Spectrum Disorders in a Total Population Sample
Abstract
Section:
Next section
A strikingly higher prevalence of autism spectrum disorders (2.6%) than previous estimates was found in South Korean children ages 7–12.
Objective:
Experts disagree about the causes and significance of the recent increases in the prevalence of autism spectrum disorders (ASDs). Limited data on population base rates contribute to this uncertainty. Using a population-based sample, the authors sought to estimate the prevalence and describe the clinical characteristics of ASDs in school-age children.
Method:
The target population was all 7- to 12-year-old children (N=55,266) in a South Korean community; the study used a high-probability group from special education schools and a disability registry and a low-probability, general-population sample from regular schools. To identify cases, the authors used the Autism Spectrum Screening Questionnaire for systematic, multi-informant screening. Parents of children who screened positive were offered comprehensive assessments using standardized diagnostic procedures.
Results:
The prevalence of ASDs was estimated to be 2.64% (95% CI=1.91–3.37), with 1.89% (95% CI=1.43–2.36) in the general-population sample and 0.75% (95% CI=0.58–0.93) in the high-probability group. ASD characteristics differed between the two groups: the male-to-female ratios were 2.5:1 and 5.1:1 in the general population sample and high-probability group, respectively, and the ratios of autistic disorders to other ASD subtypes were 1:2.6 and 2.6:1, respectively; 12% in the general-population sample had superior IQs, compared with 7% in the high-probability group; and 16% in the general-population sample had intellectual disability, compared with 59% in the high-probability group.
Conclusions:
Two-thirds of ASD cases in the overall sample were in the mainstream school population, undiagnosed and untreated. These findings suggest that rigorous screening and comprehensive population coverage are necessary to produce more accurate ASD prevalence estimates and underscore the need for better detection, assessment, and services.

 

 

Vaccine News – Shocker study unwittingly links vaccines to autism by Jon Rappoport

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).

Testimony about the flu vaccine

Want some tips for fighting the medical tyrants attempting to take control of our kids? “Go Ugly Early.” It comes from Army Survival School. Find out what it means!
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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.

Potential Carcinogens, Neurotoxins, and Seizure-Causing Chemicals in the Flu Vaccine (full breakdown of ingredients)
by Yelena Sukhoterina | September 20, 2016

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.

 

Vaccine News – Warning: Sharing this video will provoke cognitive dissonance amongst some of your friends, they may lash out in anger!

Flu shots contain mercury CDC confirms it causes tics

CDC Whistle Blower Full Audio
Brian Hooker legally recorded these phone conversations with CDC scientist and whistle blower, Dr. William Thompson on the following dates:
May 8, 2014
May 24, 2014
June 12, 2014
July 28, 2014
Why is Thimerosal Still in Vaccines?

the In honor of International Vaccine Injury Awareness Day tomorrow, June 3, here is an exclusive new clip from “Injecting Aluminum” with Dr. Chris Exley who discusses how there are no safe levels of aluminum, and how the leading health organizations worldwide have not done accurate safety studies on aluminum before using it as a vaccine adjuvant.
To learn more about the risks of aluminum in vaccines, watch the full length version of “Injecting Aluminum” here: http://www.injectingaluminum.com
Our hearts and prayers are with all who have been injured or killed by vaccines. Vaccine injury is NOT rare.

Tens of thousands marching in the streets in Warsaw, #Poland
“The state does NOT own our children!!!” This is what UPRISING looks like!
LIKE their page >>> facebook.com/stowarzyszeniestopnop
“Vaccines REVEALED” … 9 part docu-series playing now for FREE: tiny.cc/FreeVaccinationEducation
More info: http://stopnop.com.pl/poland-calls-the-whole-world-to-prote…
“3 czerwca 2017 r. zdeterminowani rodzice z dziećmi zalali ulice Warszawy protestując przeciw przymusowi szczepień. Liczba uczestników przekroczyła najśmielsze marzenia! STOP NOP apeluje do lekarzy: CHODŹCIE Z NAMI!”
“June 3, 2017, determined parents with their children flooded the streets of Warsaw protesting against compulsory vaccination. The number of participants exceeded our wildest dreams! STOP NOP urges doctors: Come join us!”
Education is empowerment – Happening now: tiny.cc/FreeVaccinationEducation
Networking, exemption information and doctor resources: tinyurl.com/RevolutionForVaccineChoice
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Not Just Autism, Major Yale Study Shows Vaccines Tied To Multiple Brain Disorders
Scientist found a strong correlation between vaccines and developing a brain disorder such as OCD, anorexia, ADHD, and major depressive disorders.
It is no question that the subject of vaccines is profoundly controversial. On both sides of the argument exist truths and lies that can hinder the ability of some to make rational decisions.
For the last 50 years, the world has taken a front row seat to the phenomenological occurrences of the rise of brain disorders such as Autism, ADHD, and major depressive disorders. Anecdotally speaking, parents all over the globe have reported that one day their children were normal and growing healthily, and the next, after having gotten their vaccinations, they get Autism, or ADHD, for example.
While science and the government continue to maintain there’s no causal relation between the vaccines and the disorders, parents, multiple studies, and other countries have reported otherwise. Now, it seems, some very brave and unabashed scientists have been able to show a correlation of what many have known for quite some time.
It has also been proven that CDC scientists destroyed data that showed a correlation between vaccines and autism in children.
Researchers at Pennsylvania State and Yale University sought to examine, “whether antecedent vaccinations are associated with increased incidence of obsessive–compulsive disorder (OCD), anorexia nervosa (AN), anxiety disorder, chronic tic disorder, attention deficit hyperactivity disorder, major depressive disorder, and bipolar disorder in a national sample of privately insured children.”

Temporal Association of Certain Neuropsychiatric Disorders Following Vaccination of Children and Adolescents: A Pilot Case–Control Study
Results: Subjects with newly diagnosed AN were more likely than controls to have had any vaccination in the previous 3 months [hazard ratio (HR) 1.80, 95% confidence interval 1.21–2.68]. Influenza vaccinations during the prior 3, 6, and 12 months were also associated with incident diagnoses of AN, OCD, and an anxiety disorder. Several other associations were also significant with HRs greater than 1.40 (hepatitis A with OCD and AN; hepatitis B with AN; and meningitis with AN and chronic tic disorder).
Conclusion: This pilot epidemiologic analysis implies that the onset of some neuropsychiatric disorders may be temporally related to prior vaccinations in a subset of individuals. These findings warrant further investigation, but do not prove a causal role of antecedent infections or vaccinations in the pathoetiology of these conditions. Given the modest magnitude of these findings in contrast to the clear public health benefits of the timely administration of vaccines in preventing mortality and morbidity in childhood infectious diseases, we encourage families to maintain vaccination schedules according to CDC guidelines.

Heavy Metals Increase Autism Risk: Scientists study babies teeth to measure exposure to metals

Hi folks. Successful rally today at Town Hall in Sydney. A short video preview until we put together a full length one.

Forbidden History: Did You Know that Raggedy Ann is an Iconic symbol for Vaccine Induced Injury and Death?
by PAUL FASSA
Johnny Gruelle created the Quintessential Raggedy Ann doll in 1915 (US patent D47789). Gruelle was a successful American writer, cartoonist, storyteller and illustrator who worked for a popular magazine at the time called Physical Culture.
Many are unaware that Gruelle’s famous Raggedy Ann storybooks and illustrations were based in large part on Marcella’s childhood adventures.
Marcella’s Vaccine Tragedy
Not long after the creation of the much beloved Raggedy Ann, Gruelle’s only child and 13 year old daughter Marcella died a painful death after receiving a routine small pox vaccination at school, which was given without parental consent.
Reports indicate that after the initial inoculation Marcella had, “… lost her appetite, and became feverish and fatigued.” Amazingly, more inoculations were given despite her negative reaction from the first jab.  Predictably Marcella’s health continued to decline to the point where she lost all muscle control, “becoming listless and lifeless like a rag doll.”
While all this was going on at school, her parents knew nothing about it and had never ever given their consent for any vaccinations.
Sadly, Marcella died a slow and agonizing death. The Gruelle’s were convinced beyond any doubt that the vaccination was the culprit behind the death of their only child, even though school authorities and vaccination proponents insisted Marcella had died from a preexisting heart defect.
Ultimately, “Seven leading physicians are called upon to opine about the cause of her death. Six consented it is the result of vaccine induced poisoning and call it malpractice. The seventh, being the head of the school board and a supporter of vaccination, declines to comment.”

MERCK’S DIRTY LITTLE SECRET – BY DR. SUZANNE HUMPHRIES
#vaxxed #PrayBig #science #truth

vaccines talk from 2 Mississippi girls #vaxxed #praybig

Warning: Sharing this video will provoke cognitive dissonance amongst some of your friends, they may lash out in anger! Why? Because the narrative that vaccines saved humanity is challenged, and it’s challenged with the CDC’s own data. Sorry, I’m not going to stop talking about these things. Vaxtremists just LIE, and they lie when the data is hiding in plain sight. Don’t believe me? The data Dr. Palevsky cites is available in the first links, read the CDC’s own data for yourself.
“Thus vaccination does not account for the impressive declines in mortality seen in the first half of the century…nearly 90% of the decline in infectious disease mortality among US children occurred before 1940, when few antibiotics or vaccine were available.”
#RFKcommission

 

Vaccine News – Study – INFANTS RECEIVING MERCURY-CONTAINING VACCINES DEVELOPED SPEECH DISORDERS, SLEEP DISORDERS, AND AUTISM, ACCORDING TO CDC SCIENTISTS

Dr. Andrew Moulden: Every Vaccine Produces Harm
by John P. Thomas
Health Impact News
Canadian physician Dr. Andrew Moulden provided clear scientific evidence to prove that every dose of vaccine given to a child or an adult produces harm. The truth that he uncovered was rejected by the conventional medical system and the pharmaceutical industry. Nevertheless, his warning and his message to America remains as a solid legacy of the man who stood up against big pharma and their program to vaccinate every person on the Earth.
Dr Moulden died unexpectedly in November of 2013 at age 49.
Because of the strong opposition from big pharma concerning Dr. Moulden’s research, I became concerned that the name of this brilliant researcher and his life’s work had nearly been deleted from the internet. His reputation was being disparaged, and his message of warning and hope was being distorted and buried without a tombstone.
I prepared a series of articles as a tribute to a great physician and as a memorial to a courageous individual who was not afraid to speak the truth about medical corruption and a flawed healthcare system that does more to harm health than it does to cure disease.
This is the first in a series of four articles about Dr. Moulden — the man, the physician, and the powerful advocate for ending all vaccine use. In future articles, I will summarize his detailed scientific evidence, which shows how vaccine damage occurs. I will explain the common mechanisms behind vaccine damage and how vaccines harm the health of everyone who receives them regardless of whether or not they notice any adverse reactions at the time they take the shots.
Dr. Moulden stated:
What we have done to each other [with vaccines] has produced the most profound damage to humankind by humankind in the history of humanity. And the reason why we got here is partly because of:
Our arrogance in thinking that we know everything. In physiology and medicine we do not know everything!
[Our greed] to advance our own self-interest to make money, to sell products and to advance corporate alliances. Commercialization has overtaken the fundamental human value of “do unto others as you would have others do unto you.” When society turns toward this human value, then we would all be working together for the greater good of each other. [However, other values have become more important] I don’t care whose feet I step on or how I get there as long as my American dream is realized. I don’t care who has to pay for it on the way of getting there. [1]
Dr. Moulden’s Credibility
Was Dr. Moulden a crackpot as some sources claim, or was he a brilliant physician and researcher? This series of articles will set the record straight, and summarize the contribution that his work has made to medical knowledge.
When I evaluate the credibility of people who are unknown to me, I begin by seeking answers to a few basic questions. For example: Is this person offering opinion, or can he or she back up the claims with valid science? Does he have educational credentials? Are there other physicians and scientists who support his or her beliefs and recommendations? Is this person controlled by the pharmaceutical industry, allopathic medical associations, or the US FDA (US Food and Drug Administration)? And finally, what do Quackwatch and their friends have to say about the person?
Dr. Moulden had a PhD in Clinical Psychology and Neuropsychology. He had a master’s degree in child development, and was also a medical doctor. [2] His work was respected by other researchers who don’t march to the drumbeat of the pharmaceutical companies. Dr. Moulden was a threat to the pharmaceutical industry, and their Quackwatch family of 21 related websites treated him as an enemy. [3, 4]

Vaccine Contraindications: Six People Who Should Not Be Vaccinated
The debate surrounding vaccinations is a fierce one, and personally, I don’t like to argue about it. I’m happy to make the right choices for my family while you make the right ones for yours. (I personally have suffered adverse reactions to vaccinations.) It’s ok to have different opinions, really it is. But there are a lot of folks out there who think everyone should be vaccinated, period, and those who choose not to vaccinate should be penalized or worse.
Listen. I get that people are scared and there’s a lot of fear-mongering in the media. But let’s be realistic here: vaccinations are a medical procedure. There are risks. Vaccinations are not right for everyone. There are at least six types of people in particular who should avoid vaccinations, and below, I’ll spell it out.
Vaccine Contraindications
Just like a particular surgery or prescription medication won’t work well for everyone, vaccinations are not a good choice for everyone.
Some people, in particular, are much more likely to have adverse reactions to vaccinations, including:

– Those with an autoimmune disease
– Children born to a mother with an autoimmune disease
– Anyone who is sick
– Pregnant women
– Those who have previously had a reaction to a vaccination

One size does not fit all
Clearly, vaccinations are not the right choice for everyone, and each family should decide what is right for them and their children. When parents are aware of vaccine contraindications, they can make informed and safer choices for their children.
Please share this post so that other parents can learn about vaccine contraindications and decide if vaccination is right for their children.

USA: Highest Vaccination Rate in the World Has the Worst Health
by PAUL FASSA
That “worst health” label includes a ranking of 34th in the world with infant mortality. In other words, the USA has the 34th worst infant survival with its highest rate of vaccinations. Some are directly from multiple vaccinations administered.
But the USA leads the world in infant vaccinations, those administered during the first year after their births – 26 vaccinations during that time.
The only vaccination I recall receiving during early childhood, circa 1948, was the smallpox vaccine, the one that left a circle of shallow pockmarks on the upper arm, a non-ink tattoo that proved you had received that vaccine. Months later there was the booster shot which gave me a vacation of several days away from my first grade teacher while sitting out the chicken pox.
During Naval training the mass vaccination high pressure hand held gun that replaced syringes and needles was tried on us with the polio shot. I wound up with a vacation in the base infirmary with an extended period of the flu. Between those two, there may have been a tetanus shot or two.
From the Healthy Home Economist:

-In1950, there were 3 childhood vaccines typically given when a child entered school.
-In 1983, there were 10 recommended vaccines by the age of 6 years old (24 doses, 7 injections, 4 oral doses for polio).
-In 2010, the CDC vax schedule totaled 68 doses with more than half given by the time a child was only a year and a half old.
-In 2016, the schedule has increased to 74 doses by age 17 with 53 injections and 3 oral doses of rotavirus.

The number of vaccines included in the current childhood vaccine schedule has quadrupled over the past 60 years, with several demanding multiple injections and boosters. During this exponential rise of CDC “recommended” schedules, the health of American children has plummeted.
Autoimmune diseases, learning disabilities, food allergies, chronic ailments, and childhood obesity have all risen. The overall health of this nation ranks very low compared to all other industrialized nations, dead last in most areas.
Vaccine false dogma is so heavy hardly anyone with authority, even in mainstream media, makes the connection between poor health with high vaccination rates. Instead, more, three added for 2016, are getting enforced by mandate or coerced by pediatricians who have the right to refuse medical care on kids who aren’t vaccinated.
Destroying Health with Vaccines is Good Business

50 Studies the AAP Avoided to Mention
There is a robust, worldwide body of published science from highly esteemed scientists questioning the safety of many different aspects of vaccines-how come we never hear from them? The majority of the most compelling science has been published since 2010. Below find 50 such studies to consider, sorted chronologically, and note that these studies only represent a portion of the published work implicating vaccinations in a wide variety of negative health outcomes.
The American Academy of Pediatrics made representations to President Trump in a letter dated 2/7/2017 that are utterly indefensible and inaccurate, as any rational review of the studies below quickly demonstrates. For example, the AAP wrote:
“Claims that vaccines are unsafe when administered according to expert recommendations have been disproven by a robust body of medical literature…we write to express our unequivocal support for the safety of vaccines.”
We contend that the AAP’s statements to the President are baseless, reckless, and easily refuted. The AAP’s letter alone supports the President’s desire to field a Vaccine Safety Commission and do all we can to make vaccines as safe as possible. Please click here for a list of all 50 studies detailed below.

2017
Temporal Association of Certain Neuropsychiatric Disorders Following Vaccination of Children and Adolescents A Pilot Case–Control Study
New Quality-Control Investigations on Vaccines Micro-and Nanocontamination
2016
Behavioral abnormalities in female mice following administration of aluminum adjuvants and the human papillomavirus (HPV) vaccine Gardasil
Autoimmune/Inflammatory Syndrome Induced by Adjuvants and Sjogren’s Syndrome
Combining Childhood Vaccines at One Visit Is Not Safe
Aluminum in Childhood Vaccines Is Unsafe
Aluminium in brain tissue in familial Alzheimer’s disease
2015
Evidence that Food Proteins in Vaccines Cause the Development of Food Allergies and Its Implications for Vaccine Policy
2014
Transcriptomic Analyses of Neurotoxic Effects in Mouse Brain After Intermittent Neonatal Administration of Thimerosal
A Dose-Response Relationship between Organic Mercury Exposure from Thimerosal-Containing Vaccines and Neurodevelopmental Disorders
A comparison of temporal trends in United States autism prevalence to trends in suspected environmental factors
2013
A Population-Based Cohort Study of Undervaccination in 8 Managed Care Organizations Across the United States
Autoimmune/inflammatory syndrome induced by adjuvants (ASIA) 2013: Unveiling the pathogenic, clinical and diagnostic aspects
Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity
Autoimmune/inflammatory syndrome induced by adjuvants (Shoenfeld’s syndrome): clinical and immunological spectrum
A two-phase study evaluating the relationship between Thimerosal-containing vaccine administration and the risk for an autism spectrum disorder diagnosis in the United States
Human exposure to aluminium
Human Papilloma Virus Vaccine and Primary Ovarian Failure: Another Facet of the Autoimmune/Inflammatory Syndrome Induced by Adjuvants
2012
Risk of Febrile Seizures and Epilepsy After Vaccination With Diphtheria, Tetanus, Acellular Pertussis, Inactivated Poliovirus, and Haemophilus Influenzae Type b
Mechanisms of aluminum adjuvant toxicity and autoimmunity in pediatric populations
Neurologic adverse events following vaccination
The spectrum of ASIA: ‘Autoimmune (Auto-inflammatory) Syndrome induced by Adjuvants’
Relative trends in hospitalizations and mortality among infants by the number of vaccine doses and age, based on the Vaccine Adverse Event Reporting System (VAERS), 1990-2010
2011
Do aluminum vaccine adjuvants contribute to the rising prevalence of autism?
Maternal Thimerosal Exposure Results in Aberrant Cerebellar Oxidative Stress, Thyroid Hormone Metabolism, and Motor Behavior in Rat Pups; Sex- and Strain-Dependent Effects
2010
Interindividual variations in the efficacy and toxicity of vaccines
Sorting out the spinning of autism: heavy metals and the question of incidence
Influence of pediatric vaccines on amygdala growth and opioid ligand binding in rhesus macaque infants: A pilot study
The immunobiology of aluminium adjuvants: how do they really work?
Hepatitis B Vaccination of Male Neonates and Autism Diagnosis, NHIS 1997-2002
2009
Allergic Disease and Atopic Sensitization in Children in Relation to Measles Vaccination and Measles Infection
Long-term persistence of vaccine-derived aluminum hydroxide is associated with chronic cognitive dysfunction
Delayed acquisition of neonatal reflexes in newborn primates receiving a thimerosal-containing Hepatitis B vaccine: Influence of gestational age and birth weight
Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration
2008
Post-vaccination encephalomyelitis: Literature review and illustrative case
Thimerosal exposure in infants and neurodevelopmental disorders: An assessment of computerized medical records in the Vaccine Safety Datalink
Delay in diphtheria, pertussis, tetanus vaccination is associated with a reduced risk of childhood asthma?
Hepatitis B triple series vaccine and developmental disability in US children aged 1-9 years
2005
THE MERCURY USED AS A VACCINE PRESERVATIVE IS FAR MORE NEUROTOXIC THAN THE MERCURY FOUND IN FISH
Comparison of Blood and Brain Mercury Levels in Infant Monkeys Exposed to Methylmercury or Vaccines Containing Thimerosal
Thimerosal Neurotoxicity is Associated with Glutathione Depletion: Protection with Glutathione Precursors
2004
Activation of methionine synthase by insulin-like growth factor-1 and dopamine: a target for neurodevelopmental toxins and thimerosal
2002
UTAH STATE SCIENTISTS FIND AUTOIMMUNE REACTION TO MMR IN CHILDREN WITH AUTISM, INCLUDING AUTOIMMUNITY TO MYELIN BASIC PROTEIN, A BRAIN BUILDING-BLOCK
Abnormal Measles-Mumps-Rubella Antibodies and CNS Autoimmunity in Children with Autism
2001
Macrophagic myofasciitis lesions assess long-term persistence of vaccine derived aluminum hydroxide in muscle
2000
JAPANESE SCIENTISTS FIND VACCINE-STRAIN OF MEASLES IN THE GUTS OF CHILDREN WITH AUTISM
Detection and Sequencing of Measles Virus from Peripheral Mononuclear Cells from Patients with Inflammatory Bowel Disease and Autism
CDC SCIENTISTS ADMIT THAT 90% OF INFECTIOUS DISEASE MORTALITY DECREASE IN THE UNITED STATES HAPPENED BEFORE VACCINES WERE AVAILABLE
Annual Summary of Vital Statistics: Trends in the Health of Americans During the 20th Century
Iatrogenic exposure to mercury after hepatitis B vaccination in preterm infants
Effects of Diphtheria-Tetanus-Pertussis or Tetanus Vaccination on Allergies and Allergy-Related Respiratory Symptoms Among Children and Adolescents in the United States
1999
INFANTS RECEIVING MERCURY-CONTAINING VACCINES DEVELOPED SPEECH DISORDERS, SLEEP DISORDERS, AND AUTISM, ACCORDING TO CDC SCIENTISTS
Increased risk of developmental neurologic impairment after high exposure to thimerosal-containing vaccine in first month of life
INFECTIOUS DISEASE RATES DECLINED PRECIPITOUSLY IN THE UNITED STATES IN THE 20TH CENTURY BEFORE THE IMPLEMENTATION OF A NATIONAL VACCINE PROGRAM
Trends in Infectious Disease Mortality in the United States During the 20th Century
CDC SCIENTISTS FIND CHILDREN GIVEN THE MMR VACCINE SHED THE MEASLES VIRUS FOR AT LEAST 2 WEEKS AFTER GETTING THE VACCINE, MAKING THEM VECTORS TO SPREAD MEASLES
Detection of Measles Virus RNA in Urine Specimens from Vaccine Recipients

Vaccine news – CDC Knew Its Vaccine Program Was Exposing Children to Dangerous Mercury Levels Since 1999

World-famous scientist issues warning about genetically modified vaccines
Here’s a look at just some of the genetically modified vaccines on the market today — and the risks we know about:
RotaTeq: This is supposed to protect babies from rotavirsues, and lots of kids get three doses before they even reach six months of age. But it’s actually made from a cross between cow and human DNA, and clinical trials found that infants are twice as likely to suffer seizures within the first two weeks after they get the vaccine.
Flucelvax: This new flu jab is being marketed like crazy this time of year. But what they’re not telling you is that it was actually made by combining human flu strains with kidney cells from a cocker spaniel! And while Flucelvax has only been around for a couple years, we already know that injecting ourselves with dog DNA is bad news. The vaccine nearly doubles your risk of a painful muscle condition called myalgia.
HPV vaccines, like Gardasil: I’ve told you stories about healthy, young girls who ended up paralyzed, unable to feed themselves and incapable of even attending school shortly after getting these shots. And currently, Virginia, Rhode Island and the District of Columbia require a Gardasil shot just to attend school.
And there are a whole bunch of new genetically-spliced recombinant vaccines coming down the pike, including one for measles.
Every time scientists try to warn us about the dangers of vaccines, the mainstream bends over backwards to call them quacks. But, trust me, nobody is saying that about Stephen Hawking.
Sources:
“Most threats to humans come from technology, warns Hawking” Ian Sample, January 19, 2016, The Guardian, msn.com

Vaccines Licensed for Use in the United States

Stephen Hawking Says the Human Race is in Danger and it’s our Own Fault
I feel so smart today. It isn’t often that the scientific merit of my ideas is confirmed by Stephen Hawking.   Today, there is an article in The Guardian, reposted in the MSN news, titled, “Most threats to humans come from science and technology, warns Hawking”. Excerpt:
“Speaking to the Radio Times ahead of the BBC Reith Lecture, in which he will explain the science of black holes, Hawking said most of the threats humans now face come from advances in science and technology, such as nuclear weapons and genetically engineered viruses.”
Genetically engineered viruses? Where have I heard that before? Oh, that’s what drug companies put into vaccines that doctors, nurses and pharmacists inject directly into and/or put in the mouths of people – vaccines for illnesses that include Hepatitis B, HPV, flu, and rotavirus.
The vaccine for Hepatitis B was the first to be made from a genetically engineered virus as announced in this New York Times article from July 1986 (please see – the reader will appreciate the historical significance). Note who, in 1986, the Hepatitis B vaccine was recommended for:
Dr. Young recommended vaccinations with either hepatitis vaccine for dental and medical workers, susceptible homosexuals and drug users, the newborn children of infected women, and, among other groups, travelers to parts of the world where hepatitis B is rampant, such as southeast Asia, sub-Saharan Africa, and parts of the Middle East.
That was a couple of years before they got the no doubt economically motivated crazy idea to assault every baby born in this country with the full series of this genetically modified concoction, the first dose of which would be given by their decree when the baby is in medical custody, in hospital, within 12 hours of birth.

ALUMINUM contained in vaccines is a metalloestrogen
Study – Metalloestrogens: an emerging class of inorganic xenoestrogens with potential to add to the oestrogenic burden of the human breast.
J Appl Toxicol. 2006 May-Jun;26(3):191-7.
Abstract
Many compounds in the environment have been shown capable of binding to cellular oestrogen receptors and then mimicking the actions of physiological oestrogens. The widespread origin and diversity in chemical structure of these environmental oestrogens is extensive but to date such compounds have been organic and in particular phenolic or carbon ring structures of varying structural complexity. Recent reports of the ability of certain metal ions to also bind to oestrogen receptors and to give rise to oestrogen agonist responses in vitro and in vivo has resulted in the realisation that environmental oestrogens can also be inorganic and such xenoestrogens have been termed metalloestrogens. This report highlights studies which show metalloestrogens to include aluminium, antimony, arsenite, barium, cadmium, chromium (Cr(II)), cobalt, copper, lead, mercury, nickel, selenite, tin and vanadate. The potential for these metal ions to add to the burden of aberrant oestrogen signalling within the human breast is discussed.

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.
RD’s parents filed a case in Vaccine Court, which took over five years to settle. RD and his family faced arduous heartbreak along the way. In the ruling, a representative from the United States Department of Justice agreed that “a preponderance of the evidence establishes that petitioner’s transverse myelitis was caused-in-fact by the administration of his August 12, 2009 varicella vaccine.” [1]
RD’s lawyer, Patricia Finn, stated that:
“The injuries that RD suffered from this vaccine are severe and lifelong.  Even though he has received a significant award as far as the awards in the Vaccine Court go, no amount of money will ever compensate him for what he has lost.
But RD is an amazing young man who has not let this injury stop him in any way.  He has graduated high school with his class, attends a Tier 1 college, and has great aspirations that I know he will achieve despite the challenges he faces because of his injuries.”
RD’s Immune System Attacked His Spine

Ignoring the agency’s own scientific evidence, the CDC’s webpage stubbornly insists that the “two types of mercury to which people may be exposed—methylmercury and ethylmercury—are very different.” The new CDC study directly contradicts this assertion, “There are many commonalities/similarities in the mechanisms of toxic action of methylmercury and ethylmercury …”
The study meticulously details identical toxicity pathways shared by both forms of mercury:
Both ethyl and methyl mercury cause DNA damage or impair DNA synthesis (Burke et al. 2006; Sharpe et al. 2012; Wu et al. 2008).
Both cause oxidative stress/creation of reactive oxygen species (Dreiem and Seegal 2007; Garg and Chang 2006; Myhre et al. 2003; Sharpe et al. 2012; Yin et al. 2007).
Both decrease glutathione activity, thus providing less protection from the oxidative stress caused by MeHg and EtHg (Carocci et al. 2014; Ndountse and Chan (2008); Choi et al. 1996; Franco et al. 2006; Mori et al. 2007; Muller et al. 2001; Ndountse and Chan 2008; Wu et al. 2008).
Both cause effects on cell division by damaging the spindle apparatus during mitosis (Burke et al. 2006; Castoldi et al. 2000; Gribble et al. 2005; Kim et al. 2007; Ou et al. 1999b; Machaty et al. 1999; Rodier et al. 1984).
Both MeHg and EtHg bind to the amino acid cysteine (Clarkson 1995; Wu et al. 2008).
Both MeHg and EtHg strongly inhibit the reacylation of arachidonic acid, thus inhibiting the reincorporation of this fatty acid into membrane phospholipids (Shanker et al. 2002; Verity et al. 1994; Zarini et al. 2006).
Both cause an increase in NOS, causing an overproduction of NO (Chen et al. 2003; Chuu et al. 2001; Shinyashiki et al. 1998).
Both disrupt glutamate homeostasis (Farina et al. 2003a, b; Manfroi et al. 2004; Mutkus et al. 2005; Yin et al. 2007).
Both alter intracellular calcium homeostasis (Elferink 1999; Hare et al. 1993;Kang et al. 2006; Limke et al. 2004b; Machaty et al. 1999; Marty and Atchison1997; Minnema et al. 1987; Peng et al. 2002; Sayers et al. 1993; Sirois and Atchison, 2000; Szalai et al. 1999; Tornquist et al. 1999; Zarini et al. 2006).
Both cause effects on receptor binding/neurotransmitter release involving one or more transmitters (Basu et al. 2008; Coccini et al. 2000; Cooper et al. 2003; Fonfria et al. 2001; Ida-Eto et al. 2011; Ndountse and Chan 2008; Yuan and Atchison 2003).
“This study is a nuclear bomb detonating over the CDC,” Boyd Haley, chairman emeritus of the University of Kentucky Chemistry Department, said. “It should be getting international, front page headlines.”

Reviews of Environmental Contamination and Toxicology
Reviews of Environmental Contamination and Toxicology publishes reviews pertaining to the sources, transport, fate and effects of contaminants in the environment. The series provides a place for the publication of critical reviews of the current knowledge and understanding of environmental sciences in order to provide insight into contaminant pathways, fate and behavior in environmental compartments and the possible consequences of their presence, with multidisciplinary contributions from the fields of analytical chemistry, biochemistry, biology, ecology, molecular and cellular biology (in an environmental context), and human, wildlife and environmental toxicology. This book series does not typically consider submissions dealing with technical aspects of occupational exposure and effects in humans, wastewater treatment and effluent characterization, or remediation of contaminated sites. However, submissions addressing one of these topic areas may be considered where there exists a strong link to the receiving environment, and/or the identification of emerging contaminants of concern. All manuscripts will be peer-reviewed by experts in the field. Reviewers will be asked to consider coverage and critical appraisal of the subject, originality , relevance, and impact to the wider scientific community. Authors writing in a second language are encouraged to have their manuscript corrected by a native English speaker or by a professional editing firm. Abstracts, short communications and notes will not be accepted. Where appropriate, such submissions may be referred to our companion journal, the Bulletin of Environmental Contamination and Toxicology (BECT), while full-length research articles are typically the purview of Archives of Environmental Contaminant and Toxicology (AECT). RECT prefers extended reviews of a length including references of more than 5,000 words, and without an upper word count limit. Reviews of shorter length (i.e. where length including references of less than 5,000 words) which may be suitable for case studies, a focused topic or an applied subject of debate or interest can be submitted to AECT. Authors may directly contact the Editor-in-Chief if they wish to clarify which publication is most suited for their submission.

Mainstream News Reporting That #BigPharma Is Paying Everyone Off!
Who would have guessed?

New Study Confirms That Mercury Is Linked to Autism
Robert F. Kennedy, Jr.
Two new studies by international teams, including Egyptian scientists, have validated the link between autism and mercury.
In an article published in the journal Metabolic Brain Disease, a team of nine scientists from leading Egyptian universities and medical schools confirmed the causal role of mercury in the onset of autism.
The scientists determined the extent of mercury poisoning in children by measuring urinary excretion of organic compounds called porphyrins, which act as biomarkers for mercury toxicity. The researchers also measured blood levels of mercury and lead. The researchers found a strong relationship between mercury toxicity and the presence of autism and a direct correlation between levels of mercury toxicity and the severity of autism symptoms.
The scientists studied 100 children; 40 with autism spectrum disorder (ASD), 40 healthy individuals and 20 healthy siblings of ASD children. The results showed that the children with ASD had significantly higher mercury levels than healthy children and healthy siblings. Children with the highest mercury levels had the most severe autism symptoms.
At least six American studies have linked autism presence or severity to mercury exposure as determined by measuring urinary porphyrins. The first study, completed by Heyer et al. in 2012 (Autism Res 5:84) showed a correlation between the presence of autism and specific urinary porphyrins associated with mercury toxicity. This affirmed an earlier study by Kern et al. (2011, Pediatr Int 53:147) where specific porphyrins associated with mercury toxicity were significantly higher in ASD children as compared to non-autistic controls. Woods et al. (2010, Environ Health Perspect 118:1450) also saw disordered porphyrin metabolism in autistic kids which was not observed in non-autistic control children. This again suggested increased mercury toxicity associated with autism and autism spectrum disorder.

Study – Altered urinary porphyrins and mercury exposure as biomarkers for autism severity in Egyptian children with autism spectrum disorder
Abstract
Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder that affects social, communication, and behavioral development. Recent evidence supported but also questioned the hypothetical role of compounds containing mercury (Hg) as contributors to the development of ASD. Specific alterations in the urinary excretion of porphyrin-containing ring catabolites have been associated with exposure to Hg in ASD patients. In the present study, the level of urinary porphyrins, as biomarkers of Hg toxicity in children with ASD, was evaluated, and its correlation with severity of the autistic behavior further explored. A total of 100 children was enrolled in the present study. They were classified into three groups: children with ASD (40), healthy controls (40), and healthy siblings of the ASD children (20). Children with ASD were diagnosed using DSM-IV-TR, ADI-R, and CARS tests. Urinary porphyrins were evaluated within the three groups using high-performance liquid chromatography (HPLC), after plasma evaluation of mercury (Hg) and lead (Pb) in the same groups. Results showed that children with ASD had significantly higher levels of Hg, Pb, and the porphyrins pentacarboxyporphyrin, coproporphyrin, precoproporphyrin, uroporphyrins, and hexacarboxyporphyrin compared to healthy controls and healthy siblings of the ASD children. However, there was no significant statistical difference in the level of heptacarboxyporphyrin among the three groups, while a significant positive correlation between the levels of coproporphyrin and precoproporphyrin and autism severity was observed. Mothers of ASD children showed a higher percentage of dental amalgam restorations compared to the mothers of healthy controls suggesting that high Hg levels in children with ASD may relate to the increased exposure to Hg from maternal dental amalgam during pregnancy and lactation. The results showed that the ASD children in the present study had increased blood Hg and Pb levels compared with healthy control children indicating that disordered porphyrin metabolism might interfere with the pathology associated with the autistic neurologic phenotype. The present study indicates that coproporphyrin and precoproporhyrin may be utilized as possible biomarkers for heavy metal exposure and autism severity in children with ASD.

CDC Knew Its Vaccine Program Was Exposing Children to Dangerous Mercury Levels Since 1999
Robert F. Kennedy, Jr. and Lyn Redwood, RN, MSN
Jan. 18, 2017 08:12PM EST
Uncovered documents show that the U.S. Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) knew that infant vaccines were exposing American children to mercury far in excess of all federal safety guidelines since 1999. The documents, created by a FDA consulting toxicologist, show how federal regulators concealed the dangerous impacts and lied to the public.
PDF source
In 1997, Congress passed the FDA Modernization Act. A provision of that statute required the FDA to “compile a list of drugs that contain intentionally introduced mercury compounds, and provide a quantitative and qualitative analysis of the mercury compounds on the list.” In response, manufacturers reported the use of the mercury-based preservative, thimerosal, in more than 30 licensed vaccines.
FDA’s Center for Biologics Evaluation and Research (CBER) was responsible for adding up the cumulative exposure to mercury from infant vaccines, a simple calculation that, astonishingly, had never been performed by either the FDA or the CDC. When the agency finally performed that basic calculation, the regulators realized that a six month-old infant who received thimerosal-preserved vaccines following the recommended CDC vaccine schedule would have received a jaw dropping 187.5 micrograms of mercury.
Instead of immediately ordering the removal of thimerosal, FDA officials circled the wagons treating the public health emergency as a public relations problem. Peter Patriarca, then director of the FDA Division of Viral Products, warned his fellow bureaucrats that hasty removal of thimerosal from vaccines would:
” … raise questions about FDA being ‘asleep at the switch’ for decades by allowing a potentially hazardous compound to remain in many childhood vaccines, and not forcing manufacturers to exclude it from new products. It will also raise questions about various advisory bodies regarding aggressive recommendations for use. We must keep in mind that the dose of ethylmercury was not generated by “rocket science.” Conversion of the percentage thimerosal to actual micrograms of mercury involves ninth grade algebra. What took the FDA so long to do the calculations? Why didn’t CDC and the advisory bodies do these calculations when they rapidly expanded the childhood immunization schedule?”
The agency consulted with experts in the field of toxicology to better understand the potential impact of these exposure levels. One consultant was Barry Rumack, MD. Dr. Rumack, at the time, had a private consulting practice, Rumack Consulting, where he offered “toxicologic and pharmacologic evaluation of drugs, biological and potentially toxic or hazardous agents for government and industry.” After creating several scenarios based on infants’ ages and weights, Dr. Rumack modeled blood and body burden levels in 1999.

Local authority is granted permission by a top judge to forcibly vaccinate a seven-month-old baby boy against his mother’s wishes despite claims she has bad reactions to jabs in the past
The London Borough of Barnet can vaccinate the seven-month-old baby boy
The boy’s mother says her other children had bad reactions from immunisations
But Barnet said potential consequence of not immunising was too great to risk
Mr Justice MacDonald has said that vaccination is in the boy’s best interests
The jabs will protect the baby against bacterial infections which can lead to highly dangerous forms of meningitis

November 7, 2002
Vaccination Safety, Part 1 In the first part of a day-long conference on the safety of various vaccination programs, participants talked about possible adverse effects of certain vaccines, the scientific community’s response to potential problems, public education efforts and the viability of mass, mandatory vaccination programs

Missouri Bill Would Ban Mercury Vaccines; First Step to Nullify Federal Policy in Practice
JEFFERSON CITY, Mo. (Jan. 31, 2017) – A Missouri House bill would ban public health clinics from administering vaccines that contain mercury or any other metal put into the vaccine for preservation purposes, contradicting approved federal policy.
House Bill 331 (HB331) was introduced by Rep. Lynn Morris (R-Nixa) to mitigate concerns regarding vaccine safety. With the exception of health emergencies determined by the Department of Health & Senior Services with concurrence from the governor, the following provision would apply:
Beginning August 28, 2018, no vaccine containing mercury or other metal for preservation or other purpose shall be administrated to a child or adult in a public health clinic in Missouri.
HB331 begins the process of nullifying potential vaccine mandates, which generally have their basis in federal recommendations or guidelines from the Centers for Disease Control and Prevention (CDC). Although these federal rules are not technically binding, they often influence policy-makers and individuals at the local and state levels to adopt coercive mandates regarding mercury-laced vaccines and other toxic substances.
By taking the rule-making power back into their own hands, the state of Missouri can disconnect from federal control and restore its sovereignty on this key issue.
NECESSITY
Measures such as HB331 push back against federal narratives regarding immunizations. The Food and Drug Administration (FDA) downplays concerns regarding the use of thimerosal, a preservative containing mercury. They even admit on their own website that mercury is still being used to preserve certain vaccines:
Thimerosal, which is approximately 50% mercury by weight, has been one of the most widely used preservatives in vaccines… While the use of mercury-containing preservatives has declined in recent years with the development of new products formulated with alternative or no preservatives, thimerosal has been used in some immune globulin preparations, anti-venins, skin test antigens, and ophthalmic and nasal products, in addition to certain vaccines.
As the FDA downplays the concerns related to thimerosal and mercury in vaccines, whistle-blowers are singing a different tune. The National Vaccine Information Center, a non-profit watchdog organization, reports that the threat is still alarming – especially pertaining to infants:
Most infants are still routinely given Thimerosal-containing influenza vaccine even though there are Thimerosal-free and vaccines with trace amounts of Thimerosal. Infants receiving a Thimerosal-containing influenza vaccine are dosed at 6 months with 12.5 mcg of ethyl mercury and at 7 months with an additional 12.5 mcg. Adult Thimerosal-containing vaccines contain roughly 25mcg.
The CDC aids the FDA in promulgating their point of view. Although the CDC attempts to maintain a veneer of independence and credibility, there are facts showing that narrative to be false. The CDC Foundation boasts that it helps the CDC “do more, faster.” It is able to do this because the CDC Foundation receives annual funding from a host of corporations including Pharmaceutical giants Merck, Roche, and Emergent BioSolutions Inc.

Fewer Same-Day Vaccines—at an Older Age, Says Study

Fewer Same-Day Vaccines—at an Older Age, Says Study
The Journal of American Physicians and Surgeons recently reported a link between the number of simultaneous vaccinations a child receives and the risk of serious injury or death. The report cites a 2012 study that looked at raw data from the government Vaccine Adverse Event Reporting System (VAERS).
The authors looked at VAERS data on infants from 1990 through 2010—about 38,000 reports in total. The study found that infants receiving multiple vaccines concurrently, as recommended by the Centers for Disease Control and Prevention (CDC), are significantly more likely to be hospitalized or die, compared with infants who received fewer vaccinations in one visit. Age was also a factor: adverse effects were more likely to lead to hospitalization or death in younger infants.
The CDC recommends a combination of up to eight vaccines during a single visit to the pediatrician. Medical literature makes it clear that this is not for the child. It is because parents cannot be trusted to bring their children back again and again to receive the full battery of vaccines. The government’s approach to vaccine administration, with one shot piled on top of another on top of another, has never been tested for safety in clinical trials.
The author points out that skeptics of using VAERS data to draw conclusions about the safety of vaccines claim that the database doesn’t prove conclusively that the adverse events reported in VAERS are caused by vaccination. But if that’s the case, why does the CDC regularly twist VAERS data to justify its recommendations?
For example, almost 9% of the adverse reactions reported for the live attenuated influenza vaccine, for example, are classified as “serious” (fatalities, cardiovascular events, neurological debilities, etc), yet CDC researchers concluded from these same adverse event reports that the results were “reassuring.” Reassuring to whom?
Speaking of the flu vaccine, a new study once again raises the question of whether mercury (still used as a flu shot preservative) increases the risk of autism.

Study: Altered urinary porphyrins and mercury exposure as biomarkers for autism severity in Egyptian children with autism spectrum disorder
Abstract
Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder that affects social, communication, and behavioral development. Recent evidence supported but also questioned the hypothetical role of compounds containing mercury (Hg) as contributors to the development of ASD. Specific alterations in the urinary excretion of porphyrin-containing ring catabolites have been associated with exposure to Hg in ASD patients. In the present study, the level of urinary porphyrins, as biomarkers of Hg toxicity in children with ASD, was evaluated, and its correlation with severity of the autistic behavior further explored. A total of 100 children was enrolled in the present study. They were classified into three groups: children with ASD (40), healthy controls (40), and healthy siblings of the ASD children (20). Children with ASD were diagnosed using DSM-IV-TR, ADI-R, and CARS tests. Urinary porphyrins were evaluated within the three groups using high-performance liquid chromatography (HPLC), after plasma evaluation of mercury (Hg) and lead (Pb) in the same groups. Results showed that children with ASD had significantly higher levels of Hg, Pb, and the porphyrins pentacarboxyporphyrin, coproporphyrin, precoproporphyrin, uroporphyrins, and hexacarboxyporphyrin compared to healthy controls and healthy siblings of the ASD children. However, there was no significant statistical difference in the level of heptacarboxyporphyrin among the three groups, while a significant positive correlation between the levels of coproporphyrin and precoproporphyrin and autism severity was observed. Mothers of ASD children showed a higher percentage of dental amalgam restorations compared to the mothers of healthy controls suggesting that high Hg levels in children with ASD may relate to the increased exposure to Hg from maternal dental amalgam during pregnancy and lactation. The results showed that the ASD children in the present study had increased blood Hg and Pb levels compared with healthy control children indicating that disordered porphyrin metabolism might interfere with the pathology associated with the autistic neurologic phenotype. The present study indicates that coproporphyrin and precoproporhyrin may be utilized as possible biomarkers for heavy metal exposure and autism severity in children with ASD.

Report: Relative trends in hospitalizations and mortality among infants by the number of vaccine doses and age, based on the Vaccine Adverse Event Reporting System (VAERS), 1990–2010
Abstract
In this study, the Vaccine Adverse Event Reporting System (VAERS) database, 1990–2010, was investigated; cases that specified either hospitalization or death were identified among 38,801 reports of infants. Based on the types of vaccines reported, the actual number of vaccine doses administered, from 1 to 8, was summed for each case. Linear regression analysis of hospitalization rates as a function of (a) the number of reported vaccine doses and (b) patient age yielded a linear relationship with r 2 = 0.91 and r 2 = 0.95, respectively. The hospitalization rate increased linearly from 11.0% (107 of 969) for 2 doses to 23.5% (661 of 2817) for 8 doses and decreased linearly from 20.1% (154 of 765) for children aged <0.1 year to 10.7% (86 of 801) for children aged 0.9 year. The rate ratio (RR) of the mortality rate for 5–8 vaccine doses to 1–4 vaccine doses is 1.5 (95% confidence interval (CI), 1.4–1.7), indicating a statistically significant increase from 3.6% (95% CI, 3.2–3.9%) deaths associated with 1–4 vaccine doses to 5.5% (95% CI, 5.2–5.7%) associated with 5–8 vaccine doses. The male-to-female mortality RR was 1.4 (95% CI, 1.3–1.5). Our findings show a positive correlation between the number of vaccine doses administered and the percentage of hospitalizations and deaths. Since vaccines are given to millions of infants annually, it is imperative that health authorities have scientific data from synergistic toxicity studies on all combinations of vaccines that infants might receive. Finding ways to increase vaccine safety should be the highest priority.

Study: Combining Childhood Vaccinesat One Visit Is Not Safe
ABSTRACT
Although health authorities including the Centers for Disease Control and Prevention (CDC) claim that childhood vaccines are safe and recommend combining multiple vaccines during one visit, a review of data from the Vaccine Adverse Event Reporting System (VAERS) shows a dose-dependent association between the number of vaccines administered simultaneously and the likelihood of hospitalization or death for an adverse reaction. Additionally, younger age at the time of the adverse reaction is associated with a higher risk of hospitalization or death

New Study Confirms That Mercury Is Linked to Autism

New Study Confirms That Mercury Is Linked to Autism
Two new studies by international teams, including Egyptian scientists, have validated the link between autism and mercury.
In an article published in the journal Metabolic Brain Disease, a team of nine scientists from leading Egyptian universities and medical schools confirmed the causal role of mercury in the onset of autism.

Study: Altered urinary porphyrins and mercury exposure as biomarkers for autism severity in Egyptian children with autism spectrum disorder
Abstract
Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder that affects social, communication, and behavioral development. Recent evidence supported but also questioned the hypothetical role of compounds containing mercury (Hg) as contributors to the development of ASD. Specific alterations in the urinary excretion of porphyrin-containing ring catabolites have been associated with exposure to Hg in ASD patients. In the present study, the level of urinary porphyrins, as biomarkers of Hg toxicity in children with ASD, was evaluated, and its correlation with severity of the autistic behavior further explored. A total of 100 children was enrolled in the present study. They were classified into three groups: children with ASD (40), healthy controls (40), and healthy siblings of the ASD children (20). Children with ASD were diagnosed using DSM-IV-TR, ADI-R, and CARS tests. Urinary porphyrins were evaluated within the three groups using high-performance liquid chromatography (HPLC), after plasma evaluation of mercury (Hg) and lead (Pb) in the same groups. Results showed that children with ASD had significantly higher levels of Hg, Pb, and the porphyrins pentacarboxyporphyrin, coproporphyrin, precoproporphyrin, uroporphyrins, and hexacarboxyporphyrin compared to healthy controls and healthy siblings of the ASD children. However, there was no significant statistical difference in the level of heptacarboxyporphyrin among the three groups, while a significant positive correlation between the levels of coproporphyrin and precoproporphyrin and autism severity was observed. Mothers of ASD children showed a higher percentage of dental amalgam restorations compared to the mothers of healthy controls suggesting that high Hg levels in children with ASD may relate to the increased exposure to Hg from maternal dental amalgam during pregnancy and lactation. The results showed that the ASD children in the present study had increased blood Hg and Pb levels compared with healthy control children indicating that disordered porphyrin metabolism might interfere with the pathology associated with the autistic neurologic phenotype. The present study indicates that coproporphyrin and precoproporhyrin may be utilized as possible biomarkers for heavy metal exposure and autism severity in children with ASD.

http://www.ecowatch.com/tag/autism

30 Solid Scientific Studies That Prove Vaccines Cause Autism
Patients MUST be able to make their own informed vaccine decisions, because often, they know more about potential vaccine risks that even top public health officials do.
1. Hepatitis B Vaccination of Male Neonates and Autism
Annals of Epidemiology, September 2009
CM Gallagher, MS Goodman, Stony Brook University Medical Center
Boys vaccinated as neonates had threefold greater odds for autism diagnosis compared to boys never vaccinated or vaccinated after the first month of life.
2. Porphyrinuria in childhood autistic disorder: Implications for environmental toxicity
Toxicology and Applied Pharmacology, 2006
Robert Natafa, et al, Laboratoire Philippe Auguste, Paris, France
These data implicate environmental toxicity in childhood autistic disorder.
3. Theoretical aspects of autism: Causes—A review
Journal of Immunotoxicology, January-March 2011
Helen V. Ratajczak, PhD
Autism could result from more than one cause, with different manifestations in different individuals that share common symptoms. Documented causes of autism include genetic mutations and/or deletions, viral infections, and encephalitis following vaccination.
4. Uncoupling of ATP-mediated Calcium Signaling and Dysregulated IL-6 Secretion in Dendritic Cells by Nanomolar Thimerosal
Environmental Health Perspectives, July 2006.
Samuel R. Goth, Ruth A. Chu Jeffrey P. Gregg
This study demonstrates that very low-levels of Thimerosal can contribute to immune system disregulation.
5. Gender-selective toxicity of thimerosal
Exp Toxicol Pathol. 2009 Mar;61(2):133-6. Epub 2008 Sep 3.
Branch DR, Departments of Medicine and Laboratory Medicine and Pathobiology, University of Toronto
A recent report shows a correlation of the historical use of thimerosal in therapeutic immunizations with the subsequent development of autism; however, this association remains controversial. Autism occurs approximately four times more frequently in males compared to females; thus, studies of thimerosal toxicity should take into consideration gender-selective effects. The present study was originally undertaken to determine the maximum tolerated dose (MTD) of thimersosal in male and female CD1 mice. However, during the limited MTD studies, it became apparent that thimerosal has a differential MTD that depends on whether the mouse is male or female.
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6. Comparison of Blood and Brain Mercury Levels in Infant monkeys exposed to Vaccines Containing Thimerosal
Environmental Health Perspectives, Aug 2005.
Thomas Burbacher, PhD, University of Washington
This study demonstrates clearly and unequivocally that ethyl mercury, the kind of mercury found in vaccines, not only ends up in the brain, but leaves double the amount of inorganic mercury as methyl mercury, the kind of mercury found in fish. This work is groundbreaking because little is known about ethyl mercury, and many health authorities have asserted that the mercury found in vaccines is the “safe kind.” This study also delivers a strong rebuke of the Institute of Medicine’s recommendation in 2004 to no longer pursue the mercury-autism connection.
7. Increases in the number of reactive glia in the visual cortex of Macaca fascicularis following subclinical long-term methyl mercury exposure
Toxicology and Applied Pharmacology, 1994
Charleston JS et al, Department of Pathology, School of Medicine, University of Washington
The identities of the reactive glial cells and the implications for the long-term function and survivability of the neurons due to changes in the glial population following subclinical long-term exposure to mercury are discussed.
8. Neuroglial Activation and Neuroinflammation in the Brain of Patients with Autism
Annals of Neurology, Feb 2005.
Diana L. Vargas, MD [Johns Hopkins University]
This study, performed independently and using a different methodology than Dr. Herbert (see above) reached the same conclusion: the brains of autistic children are suffering from inflammation.
9. Autism: A Brain Disorder, or a Disorder That Affects the Brain?
Clinical Neuropsychiatry, 2005
Martha R. Herbert M.D., Ph.D., Harvard University
Autism is defined behaviorally, as a syndrome of abnormalities involving language, social reciprocity and hyperfocus or reduced behavioral flexibility. It is clearly heterogeneous, and it can be accompanied by unusual talents as well as by impairments, but its underlying biological and genetic basis in unknown. Autism has been modeled as a brain-based, strongly genetic disorder, but emerging findings and hypotheses support a broader model of the condition as a genetically influenced and systemic.
10. Activation of Methionine Synthase by Insulin-like Growth Factor-1 and Dopamine: a Target for Neurodevelopmental Toxins and Thimerosal
Molecular Psychiatry, July 2004.
Richard C. Deth, PhD [Northeastern University]
This study demonstrates how Thimerosal inhibits methylation, a central driver of cellular communication and development.
11. Validation of the Phenomenon of Autistic Regression Using Home Videotapes
Archives of General Psychiatry, 2005
Emily Werner, PhD; Geraldine Dawson, PhD, University of Washington
Conclusion This study validates the existence of early autistic regression.
12. Blood Levels of Mercury Are Related to Diagnosis of Autism: A Reanalysis of an Important Data Set
Journal of Child Neurology, 2007
M. Catherine DeSoto, PhD, Robert T. Hitlan, PhD -Department of Psychology, University of Northern Iowa
Excerpt: “We have reanalyzed the data set originally reported by Ip et al. in 2004 and have found that the original p value was in error and that a significant relation does exist between the blood levels of mercury and diagnosis of an autism spectrum disorder. Moreover, the hair sample analysis results offer some support for the idea that persons with autism may be less efficient and more variable at eliminating mercury from the blood.”
13. Developmental Regression and Mitochondrial Dysfunction in a Child With Autism
Journal of Child Neurology, February 2006
Jon S. Poling, MD, PhD, Department of Neurology and Neurosurgery, Johns Hopkins Hospital
Excerpt: “Children who have (mitochondrial-related) dysfunctional cellular energy metabolism might be more prone to undergo autistic regression between 18 and 30 months of age if they also have infections or immunizations at the same time.”
14. Oxidative Stress in Autism: Elevated Cerebellar 3-nitrotyrosine Levels
American Journal of Biochemistry and Biotechnology, 2008
Elizabeth M. Sajdel-Sulkowska, – Dept of Psychiatry, Harvard Medical School
Excerpt: The preliminary data suggest a need for more extensive studies of oxidative stress, its relationship to the environmental factors and its possible attenuation by antioxidants in autism.”
15. Large Brains in Autism: The Challenge of Pervasive Abnormality
The Neuroscientist, 2005.
Martha Herbert, MD, PhD, Harvard University
This study helps refute the notion that the brains of autistic children are simply wired differently and notes, “neuroinflammation appears to be present in autistic brain tissue from childhood through adulthood.” Dr. Herbert suggests that chronic disease or an external environmental source (like heavy metals) may be causing the inflammation.
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16. Evidence of Toxicity, Oxidative Stress, and Neuronal Insult in Autism
Journal of Toxicology and Environmental Health, Nov-Dec 2006.
Janet Kern, Anne Jones, Department of Psychiatry, University of Texas Southwestern Medical Center
“This article discusses the evidence for the case that some children with autism may become autistic from neuronal cell death or brain damage sometime after birth as result of insult; and addresses the hypotheses that toxicity and oxidative stress may be a cause of neuronal insult in autism… the article discusses what may be happening over the course of development and the multiple factors that may interplay and make these children more vulnerable to toxicity, oxidative stress, and neuronal insult.”
17. Oxidative Stress in Autism
Pathophysiology, 2006.
Abha Chauhan, Ved Chauhan
This study provides a helpful overview of the growing evidence supporting the link between oxidative stress and autism.
18. Thimerosal Neurotoxicity is Associated with Glutathione Depletion: Protection with Glutathione Precursors
Neurotoxicology, Jan 2005.
S. Jill James, PhD, University of Arkansas
This recent study demonstrates that Thimerosal lowers or inhibits the body’s ability to produce Glutathione, an antioxidant and the body’s primary cellular-level defense against mercury.
19. Aluminum adjuvant linked to gulf war illness induces motor neuron death in mice
Neuromolecular Medicine, 2007
Christopher Shaw, Ph.D., Department of Ophthalmology and Program in Neuroscience, University of British Columbia
This study demonstrates the extreme toxicity of the aluminum adjuvant used as a preservative in vaccines.
20. Environmental mercury release, special education rates, and autism disorder: an ecological study of Texas
Health & Place, 2006
Raymond F. Palmer, University of Texas Health Science Center
This study demonstrated the correlation between environmental mercury and autism rates in Texas.
21. Autism Spectrum Disorders in Relation to Distribution of Hazardous Air Pollutants in the SF Bay Area
Environmental Health Perspectives, September, 2006
Gayle Windham, Div. of Environmental and Occupational Disease Control, California Department of Health Services
Excerpt: “Our results suggest a potential association between autism and estimated metal concentrations, and possibly solvents, in ambient air around the birth residence.”
22. A Case Series of Children with Apparent Mercury Toxic Encephalopathies Manifesting with Clinical Symptoms of Regressive Autistic Disorder
Journal of Toxicology and Environmental Health, 2007
David A. Geier, Mark R. Geier
This study reviewed the case histories and medical profiles of nine autistic children and concluded that eight of the nine children were mercury toxic and this toxicity manifested itself in a manner consistent with Autism Spectrum Disorders.
23. Attention-deficit hyperactivity disorder and blood mercury level: a case-control study in chinese children
Neuropediatrics, August 2006 – P.R. Kong
Excerpt: “There was significant difference in blood mercury levels between cases and controls, which persists after adjustment for age, gender and parental occupational status. The geometric mean blood mercury level was also significantly higher in children with inattentive and combined subtypes of ADHD. High blood mercury level was associated with ADHD. Whether the relationship is causal requires further studies.”
24. The Changing Prevalence of Autism In California
Journal of Autism and Developmental Disorders, April 2003
Mark F. Blaxill, David S. Baskin, and Walter O. Spitzer
This study helps to refute the supposition made by some researchers that autism’s epidemic may only be due to “diagnostic substitution”.
25. Mitochondrial Energy-Deficient Endophenotype in Autism
American Journal of Biochemistry and Biotechnology 2008
J. Jay Gargus and Faiqa Imtiaz, School of Medicine, University of California, Irvine,
While evidence points to a multigenic etiology of most autism, the pathophysiology of the disorder has yet to be defined and the underlying genes and biochemical pathways they subserve remain unknown.
26. Bridging from Cells to Cognition in Autism Pathophysiology: Biological Pathways to Defective Brain Function and Plasticity
American Journal of Biochemistry and Biotechnology 2008
Matthew P. Anderson, Brian S. Hooker and Martha R. Herbert, Cambridge Health Alliance/Harvard Medical School/Beth Israel Deaconess Medical Center
We review evidence to support a model where the disease process underlying autism may begin when an in utero or early postnatal environmental, infectious, seizure, or autoimmune insult triggers an immune response that increases reactive oxygen species (ROS) production in the brain that leads to DNA damage (nuclear and mitochondrial) and metabolic enzyme blockade and that these inflammatory and oxidative stressors persist beyond early development (with potential further exacerbations), producing ongoing functional consequences.
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27. Heavy-Metal Toxicity—With Emphasis on Mercury
John Neustadt, ND, and Steve Pieczenik, MD, PhD
Conclusion: Metals are ubiquitous in our environment, and exposure to them is inevitable. However, not all people accumulate toxic levels of metals or exhibit symptoms of metal toxicity, suggesting that genetics play a role in their potential to damage health.
28. Evidence of Mitochondrial Dysfunction in Autism and Implications for Treatment
American Journal of Biochemistry and Biotechnology
Daniel A. Rossignol, J. Jeffrey Bradstreet
MtD and oxidative stress may also explain the high male to female ratio found in autism due to increased male vulnerability to these dysfunctions.
29. Proximity to point sources of environmental mercury release as a predictor of autism prevalence
Health & Place, 2008
Raymond F. Palmer et al, University of Texas Health Science Center
This study should be viewed as hypothesis-generating – a first step in examining the potential role of environmental mercury and childhood developmental disorders. Nothing is known about specific exposure routes, dosage, timing, and individual susceptibility. We suspect that persistent low-dose exposures to various environmental toxicants, including mercury, that occur during critical windows of neural development among genetically susceptible children (with a diminished capacity for metabolizing accumulated toxicants) may increase the risk for developmental disorders such as autism.
30. Epidemiology of autism spectrum disorder in Portugal: prevalence, clinical characterization, and medical conditions
Developmental Medicine & Child Neurology, 2007
Guiomar Oliveira MD PhD et al, Centro de Desenvolvimento da Criança, Hospital Pediátrico de Coimbra; Assunção Ataíde BSc, Direcção Regional de Educação do Centro Coimbra;
The objective of this study was to estimate the prevalence of autistic spectrum disorder (ASD) and identify its clinical characterization, and medical conditions in a paediatric population in Portugal.