Vaccine News – Mumps Outbreak Tied to Vaccine Shortfalls

Attacking Ourselves: Top Doctors Reveal Vaccines Turn Our Immune System Against Us
Posted on: Tuesday, February 24th 2015 at 6:45 pm
Written By: Celeste McGovern
The research is hard to ignore, vaccines can trigger autoimmunity with a laundry list of diseases to follow. With harmful and toxic metals as some vaccine ingredients, who is susceptible and which individuals are more at risk?
No one would accuse Yehuda Shoenfeld of being a quack. The Israeli clinician has spent more than three decades studying the human immune system and is at the pinnacle of his profession. You might say he is more foundation than fringe in his specialty; he wrote the textbooks. The Mosaic of Autoimmunity, Autoantibodies, Diagnostic Criteria in Autoimmune Diseases, Infection and Autoimmunity, Cancer and Autoimmunity – the list is 25 titles long and some of them are cornerstones of clinical practice. Hardly surprising that Shoenfeld has been called the “Godfather of Autoimmunology” – the study of the immune system turned on itself in a wide array of diseases from type 1 diabetes to ulcerative colitis and multiple sclerosis.
But something strange is happening in the world of immunology lately and a small evidence of it is that the Godfather of Autoimmunology is pointing to vaccines – specifically, some of their ingredients including the toxic metal aluminum – as a significant contributor to the growing global epidemic of autoimmune diseases. The bigger evidence is a huge body of research that’s poured in in the past 15 years, and particularly in the past five years. Take for example, a recent article published in the journal Pharmacological Research in which Shoenfeld and colleagues issue unprecedented guidelines naming four categories of people who are most at risk for vaccine-induced autoimmunity.
“On one hand,” vaccines prevent infections which can trigger autoimmunity, say the paper’s authors, Alessandra Soriano, of the Department of Clinical Medicine and Rheumatology at the Campus Bio-Medico University in Rome, Gideon Nesher, of the Hebrew University Medical School in Jerusalem and Shoenfeld, founder and head of the Zabludowicz Center of Autoimmune Diseases in the Sheba Medical Center at Tel Hashomer. He is also editor of three medical journals and author of more than 1,500 research papers across the spectrum of medical journalism and founder of the International Congress on Autoimmunology. “On the other hand, many reports that describe post-vaccination autoimmunity strongly suggest that vaccines can indeed trigger autoimmunity. Defined autoimmune diseases that may occur following vaccinations include arthritis, lupus (systemic lupus erythematosus, SLE) diabetes mellitus, thrombocytopenia, vasculitis, dermatomyosiositis, Guillain-Barre syndrome and demyelinating disorders. Almost all types of vaccines have been reported to be associated with the onset of ASIA.”
ASIA – or Autoimmune/inflammatory Syndrome Induced by Adjuvants (also known as Shoenfeld’s syndrome) — first appeared in the Journal of Autoimmunology four years ago. It is an umbrella term for a collection of similar symptoms, including Chronic Fatigue Syndrome, that result after exposure to an adjuvant – an environmental agent including common vaccine ingredients that stimulate the immune system. Since then an enormous body of research, using ASIA as a paradigm, has begun to unravel the mystery of how environmental toxins, particularly the metal aluminum used in vaccines, can trigger an immune system chain reaction in susceptible individuals and may lead to overt autoimmune disease.
Autoimmune disease results when the body’s system meant to attack foreign invaders turns instead to attack part of the body it belongs to (auto is Greek for self). If the immune system is like a national defence system, antibodies are like drones programmed to recognize a certain type of invader (a bacteria say) and to destroy them or mark them for destruction by other special forces. Autoantibodies are like drones that are misidentifying a component of the human body and have launched a sustained attack on it. If they mistakenly target a component of the conductive sheath around neurons, for example, nerve impulses stop conducting properly, muscles go into spasm and coordination fails; multiple sclerosis results. If autoantibodies erroneously focus on joint tissue; rheumatoid arthritis results. If they target the islets of Langerhans in the pancreas, Type 1 diabetes, and so on
“Throughout our lifetime the normal immune system walks a fine line between preserving normal immune reactions and developing autoimmune diseases,” says the paper. “The healthy immune system is tolerant to self-antigens. When self-tolerance is disturbed, dysregulation of the immune system follows, resulting in emergence of an autoimmune disease. Vaccination is one of the conditions that may disturb this homeostasis in susceptible individuals, resulting in autoimmune phenomena and ASIA.”
Who is “susceptible” is the subject of the paper entitled, “Predicting post-vaccination autoimmunity: Who might be at risk?” It lists four categories of people: 1) those who have had a previous autoimmune reaction to a vaccine, 2) anyone with a medical history of autoimmunity, 3) patients with a history of allergic reactions, 4) anyone at high risk of developing autoimmune disease including anyone with a family history of autoimmunity, presence of autoantibodies which are detectable by blood tests and other factors including low vitamin D and smoking.

Study – ‘ASIA’ – autoimmune/inflammatory syndrome induced by adjuvants.
J Autoimmun. 2011 Feb
Abstract
The role of various environmental factors in the pathogenesis of immune mediated diseases is well established. Of which, factors entailing an immune adjuvant activity such as infectious agents, silicone, aluminium salts and others were associated with defined and non-defined immune mediated diseases both in animal models and in humans. In recent years, four conditions: siliconosis, the Gulf war syndrome (GWS), the macrophagic myofasciitis syndrome (MMF) and post-vaccination phenomena were linked with previous exposure to an adjuvant. Furthermore, these four diseases share a similar complex of signs and symptoms which further support a common denominator.Thus, we review herein the current data regarding the role of adjuvants in the pathogenesis of immune mediated diseases as well as the amassed data regarding each of these four conditions. Relating to the current knowledge we would like to suggest to include these comparable conditions under a common syndrome entitled ASIA, “Autoimmune (Auto-inflammatory) Syndrome Induced by Adjuvants”.

SCIENCE FACT: Chicken pox vaccine is made with “human embryonic lung cell cultures” and human diploid cell cultures from aborted fetal tissue
Monday, March 13, 2017 by: Mike Adams
(Natural News) Every individual or organization that tells you chicken pox vaccines are not made with human fetal tissue cell lines is engaged in science denialism.
It is an irrefutable science fact that varicella (chicken pox) vaccines are made with not just aborted human fetal tissue cell lines, but also cells take from guinea pigs and cows. In effect, a chicken pox vaccine is a multi-species blood and tissue cocktail of DNA and chemicals being mainlined into your tissue and blood.
This is all openly admitted by the CDC itself which lists the excipient ingredients used in common vaccines such as chicken pox, MMR and TDaP. Here’s what the CDC says is used in Varicella (chicken pox) vaccine, current as of January 6, 2017. You can see this list for yourself at this CDC.gov link. If the CDC removes their document, we’ve saved a copy at this Natural News link:
human embryonic lung cell cultures, guinea pig cell cultures, human diploid cell cultures (WI-38), human diploid cell cultures (MRC-5), sucrose, hydrolyzed gelatin, sodium chloride, monosodium L-glutamate, sodium phosphate dibasic, potassium phosphate monobasic, potassium chloride, EDTA (Ethylenediaminetetraacetic acid), neomycin, fetal bovine serum
Again, see this list for yourself at this CDC.gov link
If the CDC removes it, we’ve saved a copy at this Natural News link

Vaccine Test Results
First results of vaccine investigations
Translated by Erwin Alber from the German original Erste Ergebnisse der Impfstoffuntersuchungen published in Hans Tolzin’s newsletter impf report
(ht) In 2016, several thousand euros were donated to the non-profit association AGBUG e. V. for the investigation of the contents of currently used vaccines. We would like to thank all those who have contributed to this.
Originally, it was intended to only test the vaccines for their mercury content. The association has then however extended the focus of the investigation to include all searchable elements.
AGBUG has now published the results of the first batch on its website, so far without any evaluation! All those of you who have are knowledgeable about the toxic effects of particular elements are invited to contribute their expertise. Please send your feedback by e-mail to redaktion@impf-report.de or post under this article as a comment.

Lead, Iron, Chromium and Other Metals Routinely Contaminate Vaccine Adjuvants, Industry Study Reports
New Quality-Control Investigations on Vaccines: Micro- and Nanocontamination
Vaccine Ingredients in U.S. Vaccines – by Vaccine
Human Protein/DNA in vaccines
What You Didn’t Know About the Aborted Baby Parts in Your Vaccines

Families With Vaccine-Damaged Children Are Being Bullied Into Silence
Silencing victims of medical mishaps, is not unusual. In fact, it is almost expected these days, with “corruption” and “corporation” almost being synonymous terms.
For one family in the United Kingdom, though, things have gone to a whole new level. This family has received death threats and warnings to keep quiet about the horrible damage done to their daughter.
In 1993, the Marchant family’s 14-month-old daughter received what was supposed to be just aregular MMR vaccine. Before receiving her vaccination, baby Jodie said, “Love you!” to her dad in the waiting room at the doctor’s office. Everything seemed to be going okay — until Mr. Marchant heard his child scream.
As they would later learn,though they thought their child was being given a standard MMR vaccine, this was not the case. In fact, it turned out their child was given an untested 8-in-1 vaccine illegally — a vaccine that would permanently damage their perfectly healthy baby.
After taking their baby girl, Jodie, home from her vaccination appointment, her parents noticed she was shivering, shaking, screaming and running a fever. Like any parent would, the Marchants consulted with a doctor immediately. The doctor insisted Jodie was just suffering from a virus and there was nothing to worry about. Sadly, this would instead become the day Jodie was left permanently disabled, never again to be her normal self.
Jodie began suffering from seizures, incontinence of both bowels and bladder, and acid reflux. She also lost the ability to speak, stopped walking and no longer made eye contact. Jodie suffered with near-constant pain and was inconsolable. And with growing numbers of vaccine-damaged children being reported (and then swept under the rug), doctors merely diagnosed Jodie with autism.

Science Teacher May Be Disciplined for Urging Students Be Informed of Vaccination Risks
by Kate Raines
Published March 9, 2017
In March 2015, science teacher Timothy Sullivan approached public health nurses administering vaccines to high school students at his school in Waterford, Ontario, Canada and asked whether they had appropriately informed the students about the potential risks of the shots they were giving. He noted that the teenagers were required to give informed consent and the nurses, therefore, had the obligation to make sure they were fully informed.1
Mr. Sullivan also made the point that, “some of the components in the vaccines were deemed ‘toxic’ in his science lab.” The nurse allegedly answered that they alerted parents and teens about common vaccine risks like fever or soreness at the injection site and she claimed that “a screening tool allows nurses to assess if there are any underlying conditions that would trigger a more serious reaction among students” and added that “the risk of death from receiving a vaccine is so very, very rare.”1
Who Decides What Facts Can or Cannot Be Taught?
The complaints against Mr. Sullivan appear to have focused on how disruptive his comments were to the planned vaccination event rather than the accuracy or inaccuracy of his views. The reality of vaccine risks for death and serious side effects has been acknowledged by the U.S. Centers for Disease Control (CDC), the World Health Organization (WHO), and the U.S. National Institutes of Health (NIH). All of these organizations have stated that vaccines may cause adverse reactions and death in a small percentage of patients. According to the CDC, “although immunization has successfully reduced the incidence of vaccine-preventable diseases, vaccination can cause both minor and, rarely, serious side effects.”2
The CDC acknowledges the “possible” though “rare” association between “hepatitis B vaccine and anaphylaxis; measles vaccine and a) thrombocytopenia and b) possible risk for death resulting from anaphylaxis or disseminated disease in immunocompromised persons; diphtheria and tetanus toxoids and pertussis vaccine (DTP) and chronic encephalopathy; and tetanus-toxoid-containing vaccines and a) Guillain-Barre syndrome, b) brachial neuritis, and c) possible risk for death resulting from anaphylaxis.”2

Doctor Tearfully Apologizes to Parents (and Says NO to Vaccinating the Elderly and Vaccinating Newborns)
February 28, 2017
It’s so moving to hear this doctor apologize, also see what he thinks about vaccinating the elderly and vaccinating newborns?
You know how when someone wrongs you, even if they can’t fix the wrong, just to hear an apology feels better?  Having them acknowledge what happened, and bonus points if they really seem to care, means the world.  That must have been how Polly, from the Vaxxed movie, felt when Dr. Anthony Phan, an internal and geriatric integrative medicine doctor from Johns Hopkins, offered her a tearful and heartfelt apology for all she and other parents have been through with their vaccine-injured kids.
You can watch the entire video below, wait ’til you hear his common sense coming through!  He talks about the flawed data coming from the CDC and how he prayed asking God for insight, started reading more and learning about integrated medicine, and then stopped vaccinating his patients.  He searched for the Truth, and then STOPPED vaccinating.

Vaccine court confirms healthy 13 year-old boy was made tetraplegic by the chicken pox vaccine
Tuesday, January 03, 2017 by: Mike Adams
(Natural News) The debate about whether vaccines cause severe damage and harm to children is over. Anyone claiming vaccines cause no harm is willfully ignorant of reality, as U.S. courts have concluded, over and over again, that vaccines provably cause serious and permanent damage to children.
The latest such ruling to garner attention concerns a 13 year-old boy who was made tetraplegic (loss of function in all four limbs) following a chicken pox vaccination. After five years of battling the secretive “vaccine court” — run by Health and Human Services and founded for the purpose of denying vaccine damaged children due process via the regular court system — the evidence of harm from the vaccine was so irrefutable and conclusive that HHS had no choice but to declare the boy’s injuries were caused solely by the vaccine.
This federal courts document reveals:
On November 28, 2014, Respondent filed an amended report pursuant to Vaccine Rule
4(c) in which she concedes that Petitioner is entitled to compensation in this case. Specifically, Respondent agrees that “a preponderance of the evidence establishes that petitioner’s TM was caused-in-fact by the administration of his August 12, 2009 varicella vaccine, and that petitioner’s TM is not due to factors unrelated to the administration of the August 12, 2009 varicella vaccine.”  Amended Rule 4 Report at 1-2.
A special master may determine whether a petitioner is entitled to compensation based upon the record.  A hearing is not required … In light of Respondent’s concession and a review of the record, the undersigned finds that Petitioner is entitled to compensation.  This matter shall now proceed to the damages phase.
Vaccine proven to have seriously harmed this child… now the payoff phase begins so the vaccine industry can keep maiming other children with impunity

Mumps Outbreak Tied to Vaccine Shortfalls
By Jade Scipioni Published March 15, 2017 Health Care FOXBusiness
A CDC spokesperson tells FOX Business that while it is investigating many possible factors contributing to the increase of reported cases, it is looking into the possibility that the “protective effect of the vaccine decreases over time.”
“There hasn’t been any evidence to suggest that the MMR vaccine does not protect against circulating mumps strains. However, outbreaks have occurred in highly-vaccinated communities, particularly in close-contact settings, despite the protection afforded by mumps vaccination,” Ian Branam, a CDC press officer, tells FOX Business.
According to the CDC, MMR-II prevents most, but not all, cases of mumps and complications caused by the disease. It says two doses of the vaccine are 88% effective at protecting against mumps; one dose is 78% effective.
However, Paul Offit, MD and director of the Vaccine Education Center at The Children’s Hospital of Philadelphia, says a third dose of the vaccine may be needed in light of the current reported outbreaks, and may be a quicker solution than developing a new and stronger vaccine.
“Could you make a better mumps vaccine which has no side effects and has better protection? I think that you could, but it would probably be a two-decade long effort and it would mean a company like Merck, which is the sole manufacturer in the United States, will essentially be competing against themselves — so I don’t see that happening. I think the more likely scenario is that you give out a third dose of the current vaccine at 11 or 13 years of age,” Offit tells FOX Business.
The CDC says it is already considering whether a third dose should be added to the current immunization guidelines.
video.foxbusiness.com

Vaccine Mechanisms in Autism
Background

1983: A healthy-born child according to the CDC vaccination schedule receives 6 vaccines in the first 15 months of life. The autism rate is 1:10,000.
2017: A healthy-born child according to the CDC vaccination schedule receives 23 vaccines in the first 15 months of life. The autism rate is 1:68.

This means in the last 30 years, the prevalence of autism has risen 14,700% [3]. The projected costs for the United States would rise to more than $1 trillion by 2025 [4] if prevalence continues to rise at rates seen over last decade alone.
I want to tell you how autism comes about. Just to clarify: I am not against the concept of vaccination. I am against the toxins contained within vaccines. If you think the vaccine industry has tested all the ingredients on humans, you are deep in the woods. I invite you to examine the scientifically documented data and discover that what is happening is beyond concerning. Vaccines ARE linked to autism. And this is why.
A vaccine’s contents are injected into the muscle. From there it elicits a specific response from the immune system. Additives called adjuvants are put in vaccines to make the immune system response more pronounced and therefore more effective. The objective of adding adjuvants to vaccines is that adjuvants prime protective memory CD8 T-cells for future exposure. [29]. When your immune system is responding to the vaccine ingredients, it creates memory cells that will be ready to kill the real bacteria or virus when exposed to it in the future [6]. Vaccines have tiny particles of the virus or bacteria in it that your immune system recognizes as full blown real viral or bacterial threat.

Yale School of Medicine: Neuropsychiatric Disorders Associated with Vaccinations
March 17, 2017
by Lori M. Gregory
Health Impact News
There are questions being raised about children who are diagnosed with neuropsychiatric disorders and their association with vaccinations, according to the results of a pilot case study published in Frontiers in Psychiatry/Child & Adolescent Psychiatry [1] last month.
The study, which was conducted by researchers from the Yale University School of Medicine and the Pennsylvania State University College of Medicine Department of Public Health Sciences, is based on the principle that the immune system plays a key role in normal brain development and in the pathobiology of several neuropsychiatric disorders.  As a result, the autoimmune and inflammatory disorders affecting the central nervous system have been found to be “temporally associated with the antecedent administration of various vaccines.”
Data Suggests Link Between Influenza Vaccine and Anorexia Nervosa Diagnosis
Researchers examined the association between the administration of vaccines in children ages 6-15 years old who have been diagnosed with conditions such as anorexia nervosa, obsessive compulsive disorder (OCD), tic disorders, attention deficit hyperactivity disorder (ADHD), major depressive disorder and bipolar disorder.
What they discovered was that there is data to suggest that children who were newly diagnosed with anorexia nervosa were more likely to have been vaccinated in the previous 3 months than those in the control group.  They also found that children vaccinated with the Influenza vaccinations during the prior 3, 6, and 12 months were also associated with incident diagnoses of anorexia nervosa, OCD, and an anxiety disorder.
Several other associations were also significant, including correlations between hepatitis A with anorexia nervosa and OCD; hepatitis B with anorexia nervosa, and meningitis with anorexia nervosa and chronic tic disorder.
The principal findings suggest that children with OCD, anorexia nervosa, anxiety disorder, and tic disorder were more likely to have received influenza vaccine during the preceding year.
U.S. Special Claims Court Had 1188% Increase in Payouts for Influenza Vaccine Injury
The discovery of the possible link between the influenza vaccine and neurological disorders is significant in this study, especially in light of the fact that the U.S.Special Claims Court had a 1188% increase in payouts to Americans for influenza vaccine injury from 2014-2015 [2, 3].
(Because Congress passed a law in 1986 providing pharmaceutical companies who make vaccines with immunity from prosecution, Americans seeking compensation for vaccine injury must instead sue the U.S. Government in special claims court.)
United States Court of Federal Claims

US Vax Court Sees 400% Spike in Vaccine Injuries, Flu Shot Wins Top Honors for Biggest Payout
Vaccine injury cases are on the rise people, so if you’ve got your head in the sand and you haven’t been paying attention, it’s time to wake up.
Here’s a little background for those of you just getting started.
Ronnie Reagan… almost 30 years ago to the day, the 40th president of the United States signed away the rights of Americans to sue vaccine makers, replacing them with a law that forces families who have suffered vaccine injury or death to sue the U.S. government instead of a pharmaceutical company.
As a result, special masters from the United States Special Claims Court, also known for our purposes as the vaccine court, are given full authority as judge with no jury to decide the fate of Americans who have had the unfortunate ‘luck’ to be stricken by a vaccine injury — which can range from chronic, mild symptoms to death.
Once a year, this non-traditional court provides the public with a glimpse into its inner workings, by issuing an annual report on its website — a ritual that happens every January.  The report is sent to the President of Congress, otherwise known as the Vice President of the United States, where it is intended to serve as a bell weather monitoring reactions the American public may be having to vaccinations that are increasingly becoming forced by government mandates around the country.
Great, right?  Accountability in action?
Wrong.
The report, which is consistently ignored by mainstream media/politicians/health officials and the CDC, lies dormant on the reports page of the U.S. Special Claims Court website.
No headlines, no press release, no analysis, no alert the media, no nothing.

Vaccine News – Dr. Suzanne Humphries, M.D. – Vaccine Strain of Measles Virus Found in Measles

Dirty Vaccines: Every Human Vaccine Tested Was Contaminated With Metals and Debris in New Study
Researchers examining 44 samples of 30 different vaccines found dangerous contaminants, including red blood cells in one vaccine and metal toxicants in every single sample tested – except in one animal vaccine.
Using extremely sensitive new technologies not used in vaccine manufacturing, Italian scientists reported they were “baffled” by their discoveries which included single particles and aggregates of organic debris including red cells of human or possibly animal origin and metals including lead, tungsten, gold, and chromium, that have been linked to autoimmune disease and leukemia.
In the study, published this week in the International Journal of Vaccines and Vaccination, the researchers led by Antoinetta Gatti, of the National Council of Research of Italy and the Scientific Director of Nanodiagnostics, say their results “show the presence of micro- and nano-sized particulate matter composed of inorganic elements in vaccine samples” not declared in the products’ ingredients lists.
Lead particles were found in the cervical cancer vaccines, Gardasil and Cevarix, for example, and in the seasonal flu vaccine Aggripal manufactured by Novartis as well as in the Meningetec vaccine meant to protect against meningitis C.
Samples of an infant vaccine called Infarix Hexa (against diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis and haemophilus influenzae type B) manufactured by GlaxoSmithKline was found to contain stainless steel, tungsten and a gold-zinc aggregate.
Other metal contaminants included platinum, silver, bismuth, iron, and chromium. Chromium (alone or in alloy with iron and nickel) was identified in 25 of the human vaccines from Italy and France that were tested.
GSK’s Fluarix vaccine for children three years and older contained 11 metals and aggregates of metals. Similar aggregates to those identified in the vaccines have been shown to be prevalent in cases of leukemia, the researchers noted.
Many of the vaccines contained iron and iron alloys which, according to the researchers, “can corrode and the corrosion products exert a toxicity affecting the tissues”.
The researchers supply an image of an area in a drop of Sanofi Pasteur MSD’s Repevax (diphtheria, pertussis, tetanus, polio) vaccine “where the morphology of red cells – we cannot tell whether they are human or animal- is clearly visible” along with the presence of “debris” composed of aluminum, bromine, silicon, potassium and titanium.
Feligen, the only veterinary vaccine tested in the 44 total vaccines sampled, proved to be the only sample free from inorganic contamination.

Dirty Vaccines: New Study Reveals Prevalence of Contaminants
Posted by Celeste McGovern on Jan 30, 2017 5:31:20 PM
Every Human Vaccine Tested Was Contaminated by Unsafe Levels of Metals and Debris Linked to Cancer and Autoimmune Disease, New Study Reports
Researchers examining 44 samples of 30 different vaccines found dangerous contaminants, including red blood cells in one vaccine and metal toxicants in every single sample tested – except in one animal vaccine.
Using extremely sensitive new technologies not used in vaccine manufacturing, Italian scientists reported they were “baffled” by their discoveries which included single particles and aggregates of organic debris including red cells of human or possibly animal origin and metals including lead, tungsten, gold, and chromium, that have been linked to autoimmune disease and leukemia.
In the study, published this week in the International Journal of Vaccines and Vaccination, the researchers led by Antonietta Gatti, of the National Council of Research of Italy and the Scientific Director of Nanodiagnostics, say their results “show the presence of micro- and nano-sized particulate matter composed of inorganic elements in vaccine samples” not declared in the products’ ingredients lists.
Lead particles were found in the cervical cancer vaccines, Gardasil and Cervarix, for example, and in the seasonal flu vaccine Aggripal manufactured by Novartis as well as in the Meningetec vaccine meant to protect against meningitis C.
Samples of an infant vaccine called Infarix Hexa (against diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis and haemophilus influenzae type B) manufactured by GlaxoSmithKline was found to contain stainless steel, tungsten and a gold-zinc aggregate.

PDF source: http://medcraveonline.com/IJVV/IJVV-04-00072.pdf
Study – New Quality-Control Investigations on Vaccines: Micro-and Nanocontamination
International Journal of Vaccines and Vaccination
Abstract
Vaccines  are  being  under  investigation  for  the  possible  side  effects  they  can cause. In order to supply new information, an electron-microscopy investigation method was applied to the study of vaccines, aimed at verifying the presence of solid contaminants by means of an Environmental Scanning Electron Microscope equipped  with  an  X-ray  microprobe.  The  results  of  this  new  investigation  show the presence of micro- and nanosized particulate matter composed of inorganic elements in vaccines’ samples which is not declared among the components and whose unduly presence is, for the time being, inexplicable. A considerable part of  those  particulate  contaminants  have  already  been  verified  in  other  matrices and  reported  in  literature  as  non  biodegradable  and  non  biocompatible.  The evidence  collected  is  suggestive  of  some  hypotheses  correlated  to  diseases  that are mentioned and briefly discussed.

Parents of children with autistic spectrum disorder report extreme fatigue
Pamela Cowan, Regina Leader-Post
Published on: January 13, 2017
For more than two years, Sarah Elizabeth Ivens was fascinated to work one-on-one with children who have autism spectrum disorder.
“It’s amazing how the mind can work differently,” she said.
As she got to know the childrens’ families, Ivens was struck by the many challenges they juggled and their high level of fatigue.
“Fatigue is a sense of exhaustion that cannot be resolved by getting rest,” she said. “It’s not just being tired. If you’re tired, then you can go to bed early, sleep in and the next day you’re feeling better. That’s not the case with fatigue.”
Fatigue impacts a person’s physical and mental capacities.
Ivens completed her honours degree in psychology at the University of Victoria, and is now a PhD student in clinical psychology at the University of Regina.
Her Victoria experience spurred her to take a closer look at parents’ experiences for her master’s thesis, titled Fatigue in parents of children with Autism Spectrum Disorders: The role of parental and child factors for mothers and fathers.
“We do know from other research that fatigue is problematic for parents in general and that it can really have a big impact on their well-being and their child rearing, which results in less-effective parenting,” Ivens said.
Past research focused on mothers. For her thesis, Ivens surveyed 112 parents of children with autism between the ages of two and 12 years, with the average age being seven.
“The kids had been diagnosed three years prior, so this was not families going through the transition of learning to deal with the diagnosis,” Ivens said. “These were parents who were doing it for a few years.”
Of those answering the online questionnaires for her 2015 study, 78 were mothers and 34 were fathers.
Getting dads involved was important. In many studies, only 10 per cent are fathers, she said.
“I think their answers and experiences are really getting lost in the noise,” Ivens said.
According to existing literature, mothers report being more fatigued than fathers, the 31-year-old said.
Her survey echoed that finding.

Merck Created Hit List to “Destroy,” “Neutralize” or “Discredit” Dissenting Doctors
By Jim Edwards May 6, 2009
Merck made a “hit list” of doctors who criticized Vioxx, according to testimony in a Vioxx class action case in Australia. The list, emailed between Merck employees, contained doctors’ names with the labels “neutralise,” “neutralised” or “discredit” next to them.
According to The Australian, Merck emails from 1999 showed company execs complaining about doctors who disliked using Vioxx. One email said:
We may need to seek them out and destroy them where they live …
The plaintiffs’ lawyer gave this assessment:
It gives you the dark side of the use of key opinion leaders and thought leaders … if (they) say things you don’t like to hear, you have to neutralise them … It does suggest a certain culture within the organisation about how to deal with your opponents and those who disagree with you.
The Australian:
The court was told that James Fries, professor of medicine at Stanford University, wrote to the then Merck head Ray Gilmartin in October 2000 to complain about the treatment of some of his researchers who had criticised the drug.
“Even worse were allegations of Merck damage control by intimidation,” he wrote, … “This has happened to at least eight (clinical) investigators … I suppose I was mildly threatened myself but I never have spoken or written on these issues.”
The allegations come on the heels of revelations that Merck created a fake medical journal — the Australasian Journal of Bone and Joint Medicine — in which to publish studies about Vioxx; had pop songs commissioned about Vioxx to inspire its staff, and paid ghostwriters to draft articles about the drug.

New Merck Allegations: A Fake Journal; Ghostwritten Studies; Vioxx Pop Songs; PR Execs Harass Reporters
By Jim Edwards April 23, 2009
Federal prosecutors in the U.S. will be reading with amusement the Australian press’s coverage of a class action trial down under for patients who took Merck’s now-withdrawn painkiller Vioxx.
Details emerging in Oz make some of the antics that Merck’s American counterparts got up to look tame by comparison. For example, in Australia, Merck allegedly:
Had a doctor sign his name to an entirely ghostwritten journal article even though a Merck staffer had complained that the data within it was based on “wishful thinking.”
Created a fake “peer-reviewed” journal, the “Australasian Journal of Bone and Joint Medicine,” in which to publicize pro-Vioxx articles.
Created a Ricky Martin-style pop song to get Merck sales reps all jazzed up about Vioxx (lyrics below!).
During the trial, Merck has employed an unusually aggressive set of PR consultants, some of whom have even followed reporters into the bathroom to make sure they got the story “right.”
Hatched a Blackadder-style “cunning plan” to seed seminars with speakers who were sympathetic to Vioxx but under instructions not to mention the brand name too often.
Regarding the “wishful thinking” study, The Age reports on these emails turned over in the trial:
Email from Merck senior researcher Briggs Morrison, August 2001:
“That seems wishful thinking, not a critical interpretation of the data … The data appears to have been interpreted to support a preconceived hypothesis.”
The claim was nonetheless included in the final version of the article, which Merck employees sent to US cardiologist Dr Marv Konstam for approval.
Dr Konstam was named as the article’s lead author when it was published in the medical journal Circulation in October 2001
The Australian describes the fake journal. And The Age notes that the journal was “designed to resemble a peer-reviewed publication and reprinted previously published articles.”

Merck target of Vioxx federal grand jury probe
Mon Mar 23, 2009
Merck & Co said on Monday that it has been advised it is a target of a U.S. grand jury investigation involving its withdrawn pain drug Vioxx.
The company had previously disclosed the government probe, which has been ongoing since 2004. But it only last week received a letter from the U.S. Attorney’s office for the District of Massachusetts informing the drugmaker it is a target of the grand jury investigation, Merck said.
The probe involves Merck’s research, marketing and selling activities regarding Vioxx, the once $2.5 billion a year drug that was pulled from the market in September 2004 after a study showed it doubled the risk of heart attack and stroke in long-term users.
Merck said it has responded and will continue to respond to requests from the U.S. Attorney for documents and information in connection with the probe. The investigation includes subpoenas for witnesses to appear before a grand jury, the company has said in securities filings.
The New Jersey-based drugmaker was sued by tens of thousands of former Vioxx users who claimed to have been injured by the arthritis medicine.
After winning the majority of product liability trials that reached a jury, Merck agreed to pay $4.85 billion to settle personal injury claims from former users who had suffered heart attacks and strokes.

Study – Investigating Viruses in Cells Used to Make Vaccines; and Evaluating the Potential Threat Posed by Transmission of Viruses to Humans
Principal Investigator: Arifa S. Khan, PhD
General Overview
The emergence of pathogenic virus infections like influenza and HIV have created an urgent need for new vaccines.
Virus-based vaccines are made in living cells (cell substrates). Some manufacturers are investigating the use of new cell lines to make vaccines. The continual growth of cell lines ensures that there is a consistent supply of the same cells that can yield high quantities of the vaccine.
In some cases the cell lines that are used might be tumorigenic, that is, they form tumors when injected into rodents. Some of these tumor-forming cell lines may contain cancer-causing viruses that are not actively reproducing. Such viruses are hard to detect using standard methods. These latent, or “quiet,” viruses pose a potential threat, since they might become active under vaccine manufacturing conditions. Therefore, to ensure the safety of vaccines, our laboratory is investigating ways to activate latent viruses in cell lines and to detect the activated viruses, as well as other unknown viruses, using new technologies. We will then adapt our findings to detect viruses in the same types of cell substrates that are used to produce vaccines. We are also trying to identify specific biological processes that reflect virus activity.
These methods will enable FDA scientists to help manufacturers to determine whether their specific cell substrate is safe to use for vaccine production. The methods our laboratory are developing and testing will help to ensure the production of safe and effective vaccines in two ways: 1) FDA will be able to develop testing guidelines for manufacturers who use new cell substrates for producing vaccines; and 2) FDA will publish the new methods it develops in peer-reviewed scientific journals, thus making them readily accessible to all manufacturers.
We are also evaluating the risk of retrovirus infections in humans. (Retroviruses are RNA viruses that use an enzyme called reverse transcriptase (RT) to replicate; RNA is the de-coded form of DNA). Simian foamy virus (SFV) can be transmitted from nonhuman primates (e.g., monkeys) to humans. Although there is no evidence that SFV causes disease, the virus can remain in a lifelong quiet state in the DNA after infection. Moreover, two individuals in Africa were recently found to be infected with both HIV-1 and SFV. Therefore, it is important to determine if SFV poses a threat to human health and to understand how the virus spreads in order to create strategies for controlling human infections. Such work will also help FDA to develop a new policy regarding blood donation by individuals working with nonhuman primates and implementing formal safety guidelines for people working with SFV-infected animals. We are also investigating the consequences of dual SFV and HIV-1 infection in the monkey model.

#RFKcommission – Great video! Dartmouth-educated and Portland, OR-based Pediatrician Dr. Paul Thomas responds to Dr. Peter Hotez’s ridiculous Op-Ed in the NY Times trying to talk President Trump out of having a Vaccine Safety Commission. Oregon proud!

Dr. Suzanne Humphries, M.D. – Vaccine Strain of Measles Virus Found in Measles Outbreaks
February 21, 2017
Health Impact News Editor Comments
Dr. Suzanne Humphries is a practicing nephrologist (kidney physician). In this lecture (video below), she addresses a study done in Croatia [1] where a child who was vaccinated with the MMR vaccine was tested positive for the measles vaccine strain Schwarz eight days after vaccination.
This was a significant finding, because the child’s symptoms were thought to be similar to rubella, and without testing, the sickness would have been possibly mis-diagnosed as rubella, or the wild-type strain of measles the vaccine is designed to protect against.
This concept of “shedding,” where the child comes down with the disease from the virus in the vaccine itself, surprised the researchers:
Virus excretion in vaccinees has been reported before, but to our knowledge, this is documented for the first time for the Schwarz vaccine strain. [1]
Since 2010, this phenomena of vaccine shedding with measles in the MMR vaccine has been observed in at least two other studies:
Differentiating the wild from the attenuated during a measles outbreak. Paediatrcis and Child Health, 2012:
In the midst of a local measles outbreak, a recently immunized child was investigated for a new-onset measles-type rash. Nucleic acid testing identified that a vaccine-type measles virus was being shed in the urine. Clinically differentiating measles from a nonmeasles rash is challenging, but can be supported by a thorough medical history evaluation. Rashes are expected to occur after immunization; nucleic acid testing can be used when it is difficult to differentiate between wild and attenuated strains. [2]
Case of vaccine-associated measles five weeks post-immunisation, British Columbia, Canada, Eurosurveillance, 2013:
We describe a case of vaccine-associated measles in a two-year-old patient from British Columbia, Canada, in October 2013, who received her first dose of measles-containing vaccine 37 days prior to onset of prodromal symptoms. Identification of this delayed vaccine-associated case occurred in the context of an outbreak investigation of a measles cluster. [3]
Are health officials testing cases of measles in the current outbreak in the United States, to determine if the measles strain is the wild strain of the vaccine strain?
Not likely, and it is not likely that the mainstream media “TV doctors” will even discuss this as they falsely vilify parents who choose not to administer the MMR vaccine to their children as the cause of these outbreaks. Some of these cases are confirmed to be among those who have received the MMR vaccine, and for those who have not been vaccinated, is it possible they were infected from those recently vaccinated when the vaccine was still “shedding,” and that the vaccine-strain of measles was passed on from the vaccinated child to the unvaccinated child?

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.

Vaccine news – Measles Virus Does Not Exist

Measles Virus Does Not Exist
German biologist Dr. Stefan Lanka initially offered 100,000 euros to anyone who could provide scientific evidence that the measles virus existed. He had initially been ordered to pay up in court after Doctor David Bardens attempted to claim the prize after providing the biologist with a study that had been published in a medical journal. At that time, a Judge in the regional court in Ravensburg, South Germany, ruled in the favour of Dr. Bardens in a controversial decision claiming the criteria for evidence had been met.
The First Civil Senate of the BGH confirmed a judgment by the Higher Regional Court of Stuttgart (OLG) on in February 2016. The sum of 100,000 euros which was offered as a reward for scientific proof of the existence of the alleged measles virus did have to be paid to the plaintiff. The plaintiff also was ordered to bear all procedural costs.
Five experts have been involved in the case and presented the results of scientific studies. All five experts, including Prof. Dr. Dr. Andreas Podbielski who had been appointed by the OLG Stuttgart as the preceding court, have consistently found that none of the six publications which have been introduced to the trial, contains scientific proof of the existence of the alleged measles virus.
In the trial, the results of research into so-called genetic fingerprints of alleged measles virus have been introduced. Two recognised laboratories, including the world’s largest and leading genetic Institute, arrived at exactly the same results independently.The results prove that the authors of the six publications in the measles virus case were wrong, and as a direct result all measles virologists are still wrong today: They have misinterpreted ordinary constituents of cells as part of the suspected measles virus.
Because of this error, during decades of consensus building process, normal cell constituents were mentally assembled into a model of a measles virus. To this day, an actual structure that corresponds to this model has been found neither in a human, nor in an animal. With the results of the genetic tests, all thesis of existence of measles virus has been scientifically disproved.
The authors of the six publications and all other persons involved, did not realise the error because they violated the fundamental scientific duty, which is the need to work “lege artis”, i.e. in accordance with internationally defined rules and best practice of science. They did not carry out any control experiments. Control experiments would have protected authors and mankind from this momentous error. This error became the basis of belief in the existence of any disease-causing viruses. The expert appointed by the court, Prof. Dr. Dr. Podbielski, answering to the relevant question by the court, as per page 7 of the protocol explicitly confirmed that the authors did not conduct any control experiments.
The OLG Stuttgart overturned the judgment of the court of first instance, dismissed the action and referred, inter alia, to the central message of Prof. Podbielski with respect to the six publications. The plaintiff filed an appeal against the judgment of the OLG to the Supreme Court. As reason he stated his subjective, yet factually false perception of the trial sequence at the court in Stuttgart, and the assertion that our naming of facts about measles posed a threat to public health. The plaintiff’s position was rejected by the Supreme Court in plain words. Thus, the Supreme Court confirmed the judgment of the OLG Stuttgart from February 16, 2016.
The six publications submitted in the trial are the main relevant publications on the subject of “measles virus.” Since further to these six publications there not any other publications which would attempt by scientific methods to prove the existence of the measles virus, the Supreme Court judgment in the measles virus trial and the results of the genetic tests have consequences: Any national and international statements on the alleged measles virus, the infectivity of measles, and on the benefit and safety of vaccination against measles, are since then of no scientific character and have thus been deprived of their legal basis.
Upon enquiries which had been triggered by the measles virus contest, the head of the National Reference Institute for Measles at the Robert Koch Institute (RKI), Prof. Dr. Annette Mankertz, admitted an important fact. This admission may explain the increased rate of vaccination-induced disabilities, namely of vaccination against measles, and why and how specifically this kind of vaccination seems to increasingly trigger autism.
Prof. Mankertz has admitted that the “measles virus” contains typical cell’s natural components (ribosomes, the protein factories of the cell). Since the vaccination against measles contains whole “whole measles virus”, this vaccine contains cell’s own structures. This explains why vaccination against measles causes frequent and more severe allergies and autoimmune reactions than other types of vaccination. The court expert Prof. Podbielski stated on several occasions that by the assertion of the RKI with regard to ribosomes in the measles virus, the thesis of existence of measles virus has been falsified.
In the trial it was also put on record that the highest German scientific authority in the field of infectious diseases, the RKI, contrary to its legal remit as per 4 Infection Protection Act (IfSG), has failed to create tests for alleged measles virus and to publish these. The RKI claims that it made internal studies on measles virus, however refuses to hand over or publish the results.

OLG Stuttgart Urteil vom 16.2.2016, 12 U 63/15
Auslobung: Rechtsbindungswille bei einer negativen Auslobung; Auslegung eines Preisausschreibens hinsichtlich des Nachweises des Masernvirus
Tenor
1. Auf die Berufung des Beklagten wird das Urteil des Landgerichts Ravensburg vom 12.03.2015 – 4 O 346/13 – abgeändert und wie folgt gefasst:
(1) Der Beklagte wird verurteilt, an den Kläger 492,54 EUR nebst jährlicher Zinsen hieraus in Höhe von 5 %-Punkten über dem jeweiligen Basiszinssatz seit 16.04.2014 zu bezahlen.
(2) Im Übrigen wird die Klage abgewiesen.
2. Die weitergehende Berufung des Beklagten wird als unzulässig verworfen.
3. Die Kosten des Rechtsstreits in beiden Instanzen trägt der Kläger.
4. Das Urteil und das Urteil des Landgerichts, soweit es aufrechterhalten wird, sind vorläufig vollstreckbar.
Der Kläger kann die Vollstreckung gegen Sicherheitsleistung in Höhe von 115 % des vollstreckbaren Betrages abwenden, wenn nicht der Beklagte vor der Vollstreckung Sicherheit in Höhe von 115 % des jeweils zu vollstreckenden Betrages leistet.
5. Der Gegenstandswert für das Berufungsverfahren wird auf bis zu 110.000,00 EUR festgesetzt.

Anti-Vaxxer Biologist Stefan Lanka Bets Over $100K Measles Isn’t A Virus; He Wins In German Federal Supreme Court
Conclusions
The six publications submitted in the trial are the main relevant publications on the subject of “measles virus.” Since further to these six publications there not any other publications which would attempt by scientific methods to prove the existence of the measles virus, the Supreme Court judgment in the measles virus trial and the results of the genetic tests have consequences: Any national and international statements on the alleged measles virus, the infectivity of measles, and on the benefit and safety of vaccination against measles, are since then of no scientific character and have thus been deprived of their legal basis.
Upon enquiries which had been triggered by the measles virus contest, the head of the National Reference Institute for Measles at the Robert Koch Institute (RKI), Prof. Dr. Annette Mankertz, admitted an important fact. This admission may explain the increased rate of vaccination-induced disabilities, namely of vaccination against measles, and why and how specifically this kind of vaccination seems to increasingly trigger autism.
Prof. Mankertz has admitted that the “measles virus” contains typical cell’s natural components (ribosomes, the protein factories of the cell). Since the vaccination against measles contains whole “whole measles virus”, this vaccine contains cell’s own structures. This explains why vaccination against measles causes frequent and more severe allergies and autoimmune reactions than other types of vaccination. The court expert Prof. Podbielski stated on several occasions that by the assertion of the RKI with regard to ribosomes in the measles virus, the thesis of existence of measles virus has been falsified.
In the trial it was also put on record that the highest German scientific authority in the field of infectious diseases, the RKI, contrary to its legal remit as per § 4 Infection Protection Act (IfSG), has failed to create tests for alleged measles virus and to publish these. The RKI claims that it made internal studies on measles virus, however refuses to hand over or publish the results.
http://www.wissenschafftplus.de/uploads/article/Protokoll_13_4_20150001.pdf

Trump Warns Flu Shots Are The Greatest ‘Scam’ In Medical History
Posted on January 27, 2017 by Baxter Dmitry
The flu shot is the greatest scam in medical history, created by Big Pharma to make money off vulnerable people and make them sick, warns President Donald Trump.
In an interview with Opie and Anthony on Sirius XM, Trump slammed flu shots as “totally ineffective” and declared that he has never had one.
“I’ve never had one. And thus far I’ve never had the flu. I don’t like the idea of injecting bad stuff into your body. And that’s basically what they do. And this one (latest flu vaccine) has not been very effective to start off with.
“I have friends that religiously get the flu shot and then they get the flu. You know, that helps my thinking. I’ve seen a lot of reports that the last flu shot is virtually totally ineffective.“
Trump is right – flu shots are the greatest medical fraud in history. They are full of “bad stuff” including formaldehyde and mercury – two powerful neurotoxins – and the vaccine industry even admits that laboratory tests prove the popular jab does not work.

Study reveals 83 children awarded for damages in vaccine court have an autism diagnosis! Mary Holland, one of the study authors, says neither CDC nor Congress has ever adequately responded to this study’s claims (see study link in first comment and listen to Podcast with Mary Holland in second comment for more detail)
Please note: this story on Fox ran in 2011. The study they are reporting about was published in the NYU Law School’s legal journal, you can find a copy of it in the first comment below. NYU Law Professor Mary Holland, one of the study’s authors, noted that the CDC NEVER reposnded to the study in any way, not even to try and refute it. A podcast interview with Mary is included as the second comment, it’s a fascinating listen, thank you.

IS VACCINE INJURY ONE IN A MILLION?
With 320 million people populating the U.S. if vaccine injury is one in a million how many vaccine injuries are there? The Vaxxed Bus travels the country to see. Camera and editing by Joshua Coleman.

Dr. Rachael, featured in the documentary Vaxxed: From Cover-Up to Catastrophe & cohost of the syndicated show The Doctors, says, “I am scared of vaccines at this point,” after reviewing CDC data and hearing the stories of vaccine injury. www.StopMandatoryVaccination.com

Supreme Court of the United States 2011 – Vaccines are unsafe

US Vax Court Sees 400% Spike in Vaccine Injuries, Flu Shot Wins Top Honors for Biggest Payout
Vaccine injury cases are on the rise people, so if you’ve got your head in the sand and you haven’t been paying attention, it’s time to wake up.
Here’s a little background for those of you just getting started.
Ronnie Reagan… almost 30 years ago to the day, the 40th president of the United States signed away the rights of Americans to sue vaccine makers, replacing them with a law that forces families who have suffered vaccine injury or death to sue the U.S. government instead of a pharmaceutical company.
As a result, special masters from the United States Special Claims Court, also known for our purposes as the vaccine court, are given full authority as judge with no jury to decide the fate of Americans who have had the unfortunate ‘luck’ to be stricken by a vaccine injury — which can range from chronic, mild symptoms to death.
Once a year, this non-traditional court provides the public with a glimpse into its inner workings, by issuing an annual report on its website — a ritual that happens every January.  The report is sent to the President of Congress, otherwise known as the Vice President of the United States, where it is intended to serve as a bell weather monitoring reactions the American public may be having to vaccinations that are increasingly becoming forced by government mandates around the country.
Great, right?  Accountability in action?
Wrong.
The report, which is consistently ignored by mainstream media/politicians/health officials and the CDC, lies dormant on the reports page of the U.S. Special Claims Court website.
No headlines, no press release, no analysis, no alert the media, no nothing.
No surprise, given that most people in America don’t even know that vaccines were ruled to be unavoidably unsafe by the U.S. Supreme Court in 2011.  Also no surprise, that mainstream, co-opted, globalist elite media constantly ignore this report, along with sane arguments made by health freedom advocates about the dangers and risks of vaccine injury (‘look! a unicorn!’), instead using terms like ‘the science is in,’ and vaccine risk has been ‘debunked,’ to deter rational discussion pertaining to evidence that is hiding in plain sight.

REAGAN SIGNS BILL ON DRUG EXPORTS AND PAYMENT FOR VACCINE INJURIES
WASHINGTON, Nov. 14— President Reagan today signed a comprehensive health bill designed to promote exports of prescription drugs and to compensate children injured by vaccines.
Mr. Reagan said he had approved the bill ”with mixed feelings” because he had ”serious reservations” about the vaccine compensation program.
But he warmly endorsed provisions of the bill that would, for the first time, allow pharmaceutical companies to export drugs to other countries that have approved their use, without waiting for the United States to approve the drugs’ sale here. Mr. Reagan said this part of the new law ”will increase the competitiveness of the American pharmaceutical industry abroad, create jobs, foster biotechnology and aid other nations.” Separation-of-Powers Issue
However, he said there were ”substantial deficiencies” in the vaccine plan, under which injured people could obtain payments from the Government without proving fault or wrongdoing by the vaccine manufacturer or anyone else.
The program would be ”administered not by the executive branch, but by the Federal judiciary,” Mr. Reagan said, calling it an ”unprecedented arrangement” that was inconsistent with the constitutional requirement for separation of powers among the branches of the Federal Government.
Mr. Reagan’s action came after heavy lobbying in favor of the bill by a broad-based coalition including drug companies, physicians and groups representing children and the elderly. Agency Had Urged Veto

The United States Court of Federal Claims and the United States Court of Federal Claims Bar Association hosted their first-ever national webcast on June 19, 2013. The subject was “Meet the Office of Special Masters,” featuring introductions of the court’s two newest special masters as well as the court’s special masters answering questions from the bar.

United States court of federal claims

United States court of federal claims – Reports

Supreme Court of the United States 2011 – Vaccines are unsafe
Moreover, the Committee emphasized in its 1987 Report when it authorized funding that it had not decided, as a matter  of  law,  which,  if  any,  vaccines  were  unavoidably unsafe: “This question is left to the courts to determine in accordance with applicable law.” Id. (emphasis added). The legislative history suggests that all the stakeholders  –  Congress,  parents,  manufacturers and physicians – understood that victims preserved the  right  to  take  design  defect  claims  to  court. Respondent and its amici appear to be trying to achieve through the judiciary what they failed to obtain through Congress.

Here we present the US Federal Court’s decision and order in full below

Here we present the US Federal Court’s decision and order in full below.
The claimant in this case was dead when the damages were awarded. Tambra Harris died on November 9, 2009. Tambra’s mother and Administratix of her estate, Louvonia Deniece Harris, was substituted as petitioner, and an amended petition was filed on October 15, 2010.
Hepatitis B vaccine is given to US infants at birth for a disease which they are not at risk of.
Why? At risk groups are intravenous “recreational” drug abusers and those who practice unsafe sex – which rules out new born babies.
Whilst the risk factors for babies have changed little, there is now impressive evidence that for a preventive measure, hepatitis B vaccine is remarkable for the frequency, variety and severity of complications from its use. The toxicity of this vaccine is so unusual that, even if crucial data are regrettably concealed or covered by Court order, scientific evidence is already far higher than normally needed to justify severe restrictive measures.“
Quote from French expert Dr. Marc Girard.  See CHS article below for full details: UK Government Caught Lying On Baby Hep B Vax Safety.  Whilst other evidence is embargoed by the French Courts, Dr Girard has been able to publish a scientific review of the unembargoed evidence from the French Courts of the vaccine’s hazards (Autoimmun Rev 2005; 4: 96-100). Dr Girard shows that French health authorities suppress studies demonstrating serious risks. Hepatitis B vaccine has been shown in many peer reviewed research papers [including from Harvard University – detailed references at end] to be associated with numerous infant deaths in the USA and Europe, multiple sclerosis and numerous chronic auto-immune disorders

The controversies will find Merck defending itself and its vaccine in at least two federal court cases

The controversies will find Merck defending itself and its vaccine in at least two federal court cases after a U.S. District judge earlier this month threw out Merck’s attempts at dismissal. Merck now faces federal charges of fraud from the whistleblowers, a vaccine competitor and doctors in New Jersey and New York. Merck could also need to defend itself in Congress: The staff of representative Bill Posey (R-Fla) — a longstanding critic of the CDC interested in an alleged link between vaccines and autism — is now reviewing some 1,000 documents that the CDC whistleblower turned over to them.
The first court case, United States v. Merck & Co., stems from claims by two former Merck scientists that Merck “fraudulently misled the government and omitted, concealed, and adulterated material information regarding the efficacy of its mumps vaccine in violation of the FCA [False Claims Act].”
The second court case, Chatom Primary Care v. Merck & Co. relies on the same whistleblower evidence. This class action suit claims damages because Merck had fraudulently monopolized the mumps market. Doctors and medical practices in the suit would be able to obtain compensation for having been sold an overpriced monopolized product, and a defective one to boot, in that the mumps vaccine wasn’t effective (indeed, the suit alleged that Merck expected outbreaks to occur and, as predicted, they did — mumps epidemics occurred in 2006 in a highly vaccinated population and again in 2009-2010).