Just News – The Alex Jones Channel – Evidence Mounts Syrian WMD Attack Was False Flag

Paul Joseph Watson – Pedophiles Rule the World
International sex trafficking rings are controlled by the elite.

Infants who survive abortions are entitled to life-saving medical care, but Planned Parenthood has defended killing babies after they are born. Watch this shocking video of a Planned Parenthood lobbyist supporting infanticide.

WiFi Experiment Done By A Group Of 9th Grade Students Got Serious International Attention. THIS Is Why
April 5, 2017
They took 400 cress seeds and placed them in 12 trays. Then, they placed 6 trays in 2 separate rooms at the same temperature. They gave the same amount of water and sun to all the trays for 12 days.
However, 6 of the trays were put next to two [Wi-Fi] routers. Such routers broadcast the same type of radiation as an ordinary mobile.
After 12 days what the result spoke was clear: cress seeds next to the router did not grow, and some of them were even mutated or dead.

WATCH: An 80-year-old Catholic Priest called Father Angel has opened a Restaurant in Madrid that takes money from the rich to feed the poor — Welcome to Robin Hood Restaurant.
If you care about helping the world— Like Soul Mama now!

Top 5 Popular Children’s Snacks Made with Cancer Causing Petroleum Products
 1. Pop tarts
These toaster pastries were first introduced in 1964. The Frosted Strawberry flavor has corn syrup, high fructose corn syrup, dextrose and sugar within the first 6 ingredients! These are all forms of harmful sugar. The other alarming ingredients are TBHQ which comes from petroleum and is related to butane, partially hydrogenated soybean oil that causes cellular dysfunction, and cancer causing artificial colors.
2. Fruit snacks
These come in so many “fruit” flavors and characters they maybe hard to resist, until you realize they are made mostly is artificial additives and colors. Red 3 is a commonly used food coloring, also known as E127 or Erythrosine, a petroleum product.
3. M&M’s
They are fun colorful chocolate candies that melt in your mouth and not in your hands… These colors are artificial and are harmful when ingested. The colors utilized are, Blue #2: Is a petroleum based product that increases hyperactivity in children, increases brain tumors in lab rats and other abnormal cell development. Blue #1: Produces malignant tumors. Red #40: Damages DNA. Yellow #6: Can cause cancer and Yellow #5: All of these artificial colors are made from petroleum and can cause, in addition, allergic reactions, hyperactivity, and cancer.
4. Cheetos
Those orange, cheesy snacks. The artificial color that creates the “cheese” color is made from Yellow 6, which we know is derived from petroleum. As is the “cheese” flavoring, including, methyl benzoate and ethyl methylphenidate.
5. Teddy grahams
They have been around since 1988 and are available in 5 different flavors. These tiny bears are a great size for even small fingers but they are laced with the dreaded TBHQ. TBHQ can be toxic and also cause nausea, vomiting, ringing in the ear, delirium and collapse. It is shown to cause stomach cancer in lab rats, fragment DNA and cause damage to humane lung and umbilical cells. In children it can cause anxiety, restlessness, and intensify the symptoms of ADHD.
There are many quick and easy healthy snacks to grab and go – you don’t have to use the snacks above!

The Alex Jones Channel – Evidence Mounts Syrian WMD Attack Was False Flag
The news has done nothing but push the total war agenda after the Syrian chemical attack, but who really stands to gain from the overthrow of the Assad regime in Syria.

 

Vaccine News – THIRTY-TWO studies on vaccines SHEDDING

The Alex Jones Channel – Muppets Say Vaccines Are Safe And Pigs Fly

Get Mercury out of Medicine: World Mercury Project
Grassroots action to educate Congress and remove mercury from our medicine.
https://www.indiegogo.com/projects/get-mercury-out-of-medicine-world-mercury-project#/
Robert F. Kennedy Jr. and the World Mercury Project need your help to remove toxic mercury from pharmaceutical products. We plan to educate the public, Congress, and the media about the dangers of mercury in medicines. The FDA has already removed mercury from all over-the-counter products. It’s time to take action to remove mercury from prescription medicines including vaccines.

60 Top Vaccine Experts Unite To Inform Parents And Ensure Your Child’s Safety in This FREE Docu-Series

Dr. Rob Marvenko – “my healthy unvaccinated children” #vaxxed #Unvaxxed #truth #science #PrayBig

THIRTY-TWO studies on vaccines SHEDDING. The recently vaccinated are spreading these diseases.
CASE OF VACCINE-ASSOCIATED MEASLES FIVE WEEKS POST-IMMUNISATION

CASE OF VACCINE-ASSOCIATED MEASLES FIVE WEEKS POST-IMMUNISATION

#Measles #Shedding #Vaccine #Failure #MedScienceResearch

http://www.eurosurveillance.org/ViewArticle.aspx?ArticleId=20649

Characteristics of poliovirus strains from long-term excretors with primary immunodeficiencies.

“Individuals who are deficient in humoral immunity are particularly at risk from infection with enteroviruses, and poliovirus in particular, where antibodies are the main source of protection from disease. Long-term excretion of vaccine strains of poliovirus has been documented for many years and instances of paralytic poliomyelitis in hypogammaglobulinaemic patients who were subsequently found to have been excreting virus for prolonged periods have been reported in the U.S.A., Germany and Japan. The identification of a healthy immunodeficient patient in the U.K. who has probably been excreting type 2 poliovirus for 15 years will be described, with the characteristics of the virus and the results of attempts at treatment so far. Such individuals pose a significant risk to the eradication programme unless they can be identified and treated.”

#Shedding #Polio #Vaccine #Failure #Paralysis #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/11763340

Chronic progressive poliomyelitis secondary to vaccination of an immunodeficient child.

“We investigated an immunodeficient child in whom chronic progressive poliomyelitis developed after she had received live oral poliovirus vaccine. Poliovirus, Type II, was isolated from throat and stool during life and from several sites within the brain at autopsy.”

#Polio #Vaccine #Failure #Shedding #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/195206

Conjugal transfer vaccinia.

“Two cases of conjugal contact transfer vaccinia are described. Each patient had intimate contact after their respective partners, active-duty military personnel, received the smallpox vaccination.”

#Shedding #Smallpox #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/15337993/

Contact transmission of vaccinia virus from smallpox vaccinees in the United States, 2003-2011.

“The vaccine contains live vaccinia virus that can be transferred through physical contact.”

#Shedding #Smallpox #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/22192851/

Detection of fecal shedding of rotavirus vaccine in infants following their first dose of pentavalent rotavirus vaccine.

#Shedding #Rotavirus #Failure #Gastrointestinal #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/21477676/

Detection of measles vaccine in the throat of a vaccinated child.

#Shedding #Measles #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/11858860/

Detection of measles virus RNA in urine specimens from vaccine recipients.

#Shedding #Measles #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC228449/

Faecal shedding of canine parvovirus after modified-live vaccination in healthy adult dogs.

“Despite individual differences, CPV DNA was detectable for up to 28 days after vaccination, although the faecal CPV DNA load in these clinically healthy dogs was very low.”

#Shedding #Parvo #Dog #Animal #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/28093104/

Herpes zoster due to Oka vaccine strain of varicella zoster virus in an immunosuppressed child post cord blood transplant.

#Shingles #Shedding
#Vaccine #Failure #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/17854459

Horizontal transmission of a human rotavirus vaccine strain–a randomized, placebo-controlled study in twins.

#Shedding #Rotavirus #Vaccine #Failure #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/22008819/

Human Illness Associated with Use of Veterinary Vaccines 

#Animals #Shedding #Vaccine #MedScienceResearch

“Is human exposure to veterinary vaccines a potential public health concern? There is currently limited understanding of the incidence of exposure of individuals to veterinary vaccines or of the consequences of such exposure. In addition, the potential for exposure and for adverse consequences secondary to exposure to veterinary vaccines may be increasing. The increased development and use of veterinary vaccines (including live vaccines), the increased aerosol administration of vaccines, and the increased proportion of individuals in the United States who are immunosuppressed and who may be exposed to these vaccines or to animals shedding the vaccine strains suggest that increased vigilance may be warranted.”

http://m.cid.oxfordjournals.org/content/37/3/407.full

Interference of Vaccine Derived Polio Viruses with Diagnosis of Enteroviral Diseases in Neonatal Period.

“OPV vaccinated neonates commonly pass the vaccine virus in their pharynx and stool which can be mistaken with NPEV.”

#Shedding #Polio #Vaccine #Failure #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/28050469

Kinetics of poliovirus shedding following oral vaccination as measured by quantitative reverse transcription-PCR versus culture.

#Shedding #Polio #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/25378579/

Knowledge and attitudes towards influenza vaccination of health care workers in emergency services.

#Flu #Influenza #Shedding #Vaccines #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/27919630/

Long-term viremia and fecal shedding in pups after modified-live canine parvovirus vaccination.

#Shedding #Parvo #Animal #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/24793948/

🛑 [Mumps vaccine virus transmission].

“In this work we report the mumps vaccine virus shedding based on the laboratory confirmed cases of the mumps virus (MuV) infection. The likely epidemiological sources of the transmitted mumps virus were children who were recently vaccinated with the mumps vaccine containing Leningrad-Zagreb or Leningrad-3 MuV. The etiology of the described cases of the horizontal transmission of both mumps vaccine viruses was confirmed by PCR with the sequential restriction analysis.”

#Mumps #Vaccine #Failure #Shedding #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/24772647/

Nonfebrile Seizures after Mumps, Measles, Rubella, and Varicella-Zoster Virus Combination Vaccination with Detection of Measles Virus RNA in Serum, Throat, and Urine

#MMRV #Shedding #Seizures #Measles #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3697452/

Rotavirus shedding in premature infants following first immunization.

#Shedding #Rotavirus #Failure #Gastrointestinal #Premature #Vaccine #Premie #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/21856359/

Rotavirus vaccine-derived shedding and viral reassortants.

#Shedding #Rotavirus #Failure #Gastrointestinal #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/23249230/

Rotavirus vaccines: viral shedding and risk of transmission.

#Shedding #Rotavirus #Failure #Gastrointestinal #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/18922486/

Rubella persistence in epidermal keratinocytes and granuloma M2 macrophages in patients with primary immunodeficiencies

#Rubella #Shedding #Vaccine #MedScienceResearch

http://www.jacionline.org/retrieve/pii/S0091674916307126

Serotype-specific mucosal immune response and subsequent poliovirus replication in vaccinated children.

“In the case of poliovirus Type 3, about 10% of children were still excreting the vaccine virus 9 weeks after administering the third dose.”

#Shedding #Polio #Vaccine #Failure #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/12938203

Spotlight on measles 2010: excretion of vaccine strain measles virus in urine and pharyngeal secretions of a child with vaccine associated febrile rash illness, Croatia, March 2010.

#Measles #Shedding #Vaccine #MedScienceResearch

http://www.ncbi.nlm.nih.gov/m/pubmed/20822734/

Spread of vaccinia virus through shaving during military training, Joint Base San Antonio-Lackland, TX, June 2014.

“Adverse events following smallpox vaccination may occur in the vaccinee, in individuals who have contact with the vaccinee (i.e., secondary transmission), or in individuals who have contact with the vaccinee’s contact (i.e., tertiary transmission). In June 2014 at Joint Base San Antonio-Lackland, TX, two cases of inadvertent inoculation of vaccinia and one case of a non-viral reaction following vaccination occurred in the security forces training squadron. This includes the first reported case of shaving as the likely source of autoinoculation after contact transmission. This paper describes the diagnosis and treatment of these cases, the outbreak investigation, and steps taken to prevent future transmission.”

#Shedding #Smallpox #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/25162496/

Transmission of imported vaccine-derived poliovirus in an undervaccinated community in Minnesota.

#Polio #Vaccine #Shedding #MedScienceResearch #Failure

https://www.ncbi.nlm.nih.gov/m/pubmed/19090774/

Unintentional transfer of vaccinia virus associated with smallpox vaccines: ACAM2000(®) compared with Dryvax(®).

“We identified 309 reports for ACAM2000® with skin or ocular involvement, of which 93 were autoinoculation cases and 20 were contact transmission cases. The rate for reported cases of autoinoculation was 20.6 per 100,000 vaccinations and for contact transmission was 4.4 per 100,000 vaccinations. Eighteen contact transmission cases could be attributed to contact during a sporting activity (45%) or intimate contact (45%). Of the 113 unintentional transfer cases, 6 met the case definition for ocular vaccinia. The most common locations for all autoinoculation and contact cases were arm/elbow/shoulder (35/113; 31%) and face (24/113; 21%). Methods We reviewed 753 reports associated with smallpox in the Vaccine Adverse Event Reporting System and CDC Poxvirus consultation log, reported from March 2008 to August 2010. Reports were classified into categories based upon standard case definitions.”

#Shedding #Smallpox #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/23571177/

Use of a novel real-time PCR assay to detect oral polio vaccine shedding and reversion in stool and sewage samples after a mexican national immunization day.

“During replication, oral polio vaccine (OPV) can revert to neurovirulence and cause paralytic poliomyelitis. In individual vaccinees, it can acquire specific revertant point mutations, leading to vaccine-associated paralytic poliomyelitis (VAPP). With longer replication, OPV can mutate into vaccine-derived poliovirus (VDPV), which causes poliomyelitis outbreaks similar to those caused by wild poliovirus. After wild poliovirus eradication, safely phasing out vaccination will likely require global use of inactivated polio vaccine (IPV) until cessation of OPV circulation.”

#Shedding #Polio #Paralysis
#Vaccine #Failure
#MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/21411577

VACCINE-ASSOCIATED POLIOMYELITIS IN A CHILD WITH THYMIC ABNORMALITY

#Polio #Shedding #Death #Paralysis #Vaccine #Failure #MedScienceResearch

http://pediatrics.aappublications.org/content/48/6/923

Vaccine-associated poliomyelitis in an infant with agammaglobulinemia.

#Polio #Vaccine #Failure #Shedding #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/6255734

Varicella Zoster Virus DNA at Inoculation Sites and in Saliva After Zostavax Immunization

#Shingles #Shedding #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096786/

What is the cause of a rash after measles-mumps-rubella vaccination?

“We describe a 17-month-old child with fever and rash after measles-mumps-rubella vaccination. Detection of vaccine-strain
measles virus in his urine by poly
merase chain reaction confirmed the diagnosis of a vaccine reaction rather than wild-type measles. We propose that measles virus should be sought and identified as vaccine or wild-type virus when the relationship between vaccination and measles-like illness is uncertain.”

#Vaccine #Failure #Shedding #MMR #Measles #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/10494235

 

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 – 130 Research papers supporting Vaccine/Autism CausationGinger Taylor, MS

Gardasil: The decision we will always regret
February 4, 2014
By Kim Robinson, Red Hill, Pennsylvania
Katie’s Gardasil Experience
By all accounts, our daughter was normal before receiving the HPV vaccine.  Katie performed very well in school.  She was conscientious, hard-working and took pride in getting good grades.  She loved dancing having taken dance classes since she was 3 years old.  Katie always danced and twirled throughout our home and anywhere else she happened to be.  When Katie was 10, she joined cheerleading and became involved in competition cheerleading.  She was very active, taking four hours of dance class every week plus spending many more hours practicing with her competition cheer team.  Katie was healthy and vibrant.
We were very diligent with our children’s health.  We never missed an annual check-up and we also followed the pediatrician’s recommended vaccine schedule including annual flu shots.  Our pediatrician recommended the Gardasil vaccine.  The Gardasil vaccine was heavily advertised on TV.  We read the vaccine Disclosure.  It said that the vaccine should not be given to those with HIV.  Katie did not have HIV so we signed the Consent.
On September 2, 2010 at the age of 11, Katie received the first Gardasil vaccine.  Katie’s first day of middle school was September 7, 2010.  Initially, we believed that her fatigue and headaches were being caused by having to get up much earlier in the morning for middle school.  However, she never adjusted to the new schedule and soon her symptoms began exploding.  Katie would often tell us “I don’t know what’s wrong, I just don’t feel good.”  She began sleeping a lot – over 12 hours a day and even more on the weekends, which would allow her gather enough energy to go to school a few days before she crashed again.  She missed days at school, dance lessons and cheer practices.  Soon her illness was visible on the outside too.  Katie didn’t look good – constant dark circles under her eyes, her skin color was ashen and she appeared listless.

Gardasil Is Destroying Our Daughters And Nobody Cares!
Posted on February 20, 2017 by Jacqui Deevoy
This is the cry from Gini Blesky, one of thousands of mothers worldwide whose young daughters’ lives have been devastated by the ‘side-effects’ of government-approved HPV vaccine Gardasil.
The much-debated vaccine, developed to prevent HPV (which can lead to cervical cancer) – given to girls around the world at around the age of 12 – has been in the spotlight for some time now, with stories popping up on social media and alternative radio networks and with no thanks whatsoever to the mainstream media.
As a journalist, mother and general truth-seeker, I’ve had a personal interest in this controversial vaccine for many years. When it was first introduced, I refused to let my teenage daughters have it, after I’d tried to research it and found nothing. My general feeling at the time was that the introduction of it seemed a bit sudden and I wasn’t altogether comfortable with that.
But it was while I was trying – and failing – to get the UK mainstream media to publish a story about the dangers of this vaccine that I realized that the refusal of the publications I approached to give it any exposure was a story in itself! So here I am…
Because of my personal interest in the story (by this time, I’d met several girls whose lives and families had been severely affected by illness after the jab and I’d discovered that two families I was related to had also been affected), I was keen to put out a warning. While many countries were working on withdrawing the vaccine due to the damage it was causing, other countries – the UK and US included – were stepping up the programme. In recent months, there’s even been talk of giving the vaccine to boys.
If anyone wants an interview with Gini Blesky, please call 07514 64 366 or email jacqui.deevoy@gmail.com
To get more info about AHVID, please contact Freda Birrell on 07752 945 545 or at jeanfreda8@btinternet.com
You can contact Gini Blesky and follow Mia’s progress via Facebook: https://www.facebook.com/gini.kok
Mia’s GoFundMe appeal is at: https://www.gofundme.com/mias-recovery-fund

New Vaccines Will Permanently Alter Human DNA
Why is the government so maniacal about injecting vaccines?
by Jon Rappoport
Consider this article in light of the accelerating push to mandate and enforce vaccination across the planet.
The reference is the New York Times, 3/9/2015, “Protection Without a Vaccine.” It describes the frontier of research. Here are key quotes that illustrate the use of synthetic genes to “protect against disease,” while changing the genetic makeup of humans.
This is not science fiction:
“By delivering synthetic genes into the muscles of the [experimental] monkeys, the scientists are essentially re-engineering the animals to resist disease.”
“’The sky’s the limit,’ said Michael Farzan, an immunologist at Scripps and lead author of the new study.”
“The first human trial based on this strategy — called immunoprophylaxis by gene transfer, or I.G.T. — is underway, and several new ones are planned.”
“I.G.T. is altogether different from traditional vaccination. It is instead a form of gene therapy. Scientists isolate the genes that produce powerful antibodies against certain diseases and then synthesize artificial versions. The genes are placed into viruses and injected into human tissue, usually muscle.”
Here is the punchline:
“The viruses invade human cells with their DNA payloads, and the synthetic gene is incorporated into the recipient’s own DNA. If all goes well, the new genes instruct the cells to begin manufacturing powerful antibodies.”
Read that again: “the synthetic gene is incorporated into the recipient’s own DNA.” Alteration of the human genetic makeup. Permanent alteration.
The Times article taps Dr. David Baltimore for an opinion:
“Still, Dr. Baltimore says that he envisions that some people might be leery of a vaccination strategy that means altering their own DNA, even if it prevents a potentially fatal disease.”
Yes, some people might be leery. If they have two or three working brain cells.

Protection Without a Vaccine By CARL ZIMMERMARCH 9, 2015
Last month, a team of scientists announced what could prove to be an enormous step forward in the fight against H.I.V.
Scientists at Scripps Research Institute said they had developed an artificial antibody that, once in the blood, grabbed hold of the virus and inactivated it. The molecule can eliminate H.I.V. from infected monkeys and protect them from future infections.
But this treatment is not a vaccine, not in any ordinary sense. By delivering synthetic genes into the muscles of the monkeys, the scientists are essentially re-engineering the animals to resist disease. Researchers are testing this novel approach not just against H.I.V., but also Ebola, malaria, influenza and hepatitis.
“The sky’s the limit,” said Michael Farzan, an immunologist at Scripps and lead author of the new study.
Continue reading the main story
Dr. Farzan and other scientists are increasingly hopeful that this technique may be able to provide long-term protection against diseases for which vaccines have failed. The first human trial based on this strategy — called immunoprophylaxis by gene transfer, or I.G.T. — is underway, and several new ones are planned.
“It could revolutionize the way we immunize against public health threats in the future,” said Dr. Gary J. Nabel, the chief scientific officer of Sanofi, a pharmaceutical company that produces a wide range of vaccines.
Whether I.G.T. will succeed is still an open question. Researchers still need to gauge its safety and effectiveness in humans. And the prospect of genetically engineering people to resist infectious diseases may raise concerns among patients.

Three Examples of Pro-Vaccination Hypocrisy By Tami Canal On February 20, 2017
The common sense, or lack thereof, of some people truly baffles me and I have reached a point where I’m going to call out the hypocrisy of certain individuals. If the following offends you, I make no apologies. Instead, I encourage you to focus your outrage on the thousands of innocent victims of the CDC’s vaccination program. (Read more about that by clicking here: http://vaccineimpact.com/2016/vaccine-court-stats-on-injuries-and-deaths-betray-governments-position-on-vaccine-safety/)
If you advocate for any of the following issues, but allow your child to be vaccinated…you are a hypocrite.
1. Pro-Life
You cannot be pro-life and pro-vaccine…unless there’s a clause in the pro-life rule book that allows for the use of aborted fetal cells in vaccinations given to humans.
This is not fear-mongering or “woo”, as the trolls will cry. It’s a plain and simple fact that a minimum of 27 vaccines contain aborted fetal tissue, DNA, proteins and cells including:
-Hep A
-Hep A/Hep B Combo
-Polio
-Dtap/Polio/HiB Combo
-MMR
-MMRV Pro Quad
-Varicella
-Shingles
It’s shocking that little to no religious outcry exists and it’s mind boggling that pro-life advocates will denounce abortion, but seemingly condone the use of aborted fetal elements in vaccinations given to children.
It’s also imperative that I mention that the research that is available on the safety of injecting human DNA into another human shows that there may be radical immune responses and can even cause death.

Top government scientists refuse to vaccinate their children
By: Vicki Batts Date: August 19, 2016
How shocking is it that New Mexico, the school district with the highest percentage of students whose families are opting out of vaccines, is actually one of the state’s most scientifically literate communities?
Well, if you know how harmful vaccines really are, you might not really be all that surprised. But for many, the 2.3 percent of students forgoing traditional vaccine regimens in Los Alamos is causing quite the upset. After all, many of the parents in the community work for US Los Alamos Labs, or one of the other scientific organizations that call the area home. For example, the Los Alamos National Laboratory has even conducted extensive research and development on a vaccine for HIV.
The Superintendent of the Los Alamos school systems has said that he finds the high rate of parents exempting their children from vaccination “curious,” given that it is a “pretty scientific and literate community.”
While the mainstream media continues to come up with all kinds of wild  reasons for why “anti-vaxxers” don’t vaccinate their children, a community of scientists continues to abstain from the practice, much to the chagrin of pro-vaccine activists. Los Alamos is not alone; Santa Fe’s percentage of children not getting jabbed was just a few points behind, at 2.1 percent.
Anna Pentler, the head of the New Mexico Immunization Coalition (a pro-vaccine group) seems to think that not wanting to inject their children with toxic adjuvants and heavy metals is an “emotional issue,” and not an issue of ethics and morality. She says that while the science could be “99 to 1″ in favor of vaccines, a parent’s anecdotal story of how vaccines harmed their child could easily sway another parent’s opinion.
While it is true that the countless horror stories that many parents and children are forced to endure post-vaccination are enough to give any reasonable parent pause, the fact is that the science behind vaccine damage is also all there. The problem is that no one wants to believe it; no one wants their reality disrupted.
As the Children’s Medical Safety Research Institute states, “[T]here is a large body of scientific evidence confirming numerous vaccine safety deficits that counteract well-publicized benefits. For example, several studies show that thimerosal (mercury) and aluminum in vaccines can cause neurological, immunological and developmental harm.”
The CDC itself has conducted investigations on the harmful effects of certain ingredients in vaccines, and found that they did in fact disrupt neurological development in young children. But the mainstream media doesn’t care about that; they want you to fall in line and do your “due diligence” by getting vaccinated to maintain society’s “herd immunity” – which isn’t even real, by the way.

The Herd Immunity Myth – Treating Our Children Like Cattle
February 22, 2017
by Joanna Karpasea-Jones from VaccineRiskAwareness.com
When my oldest child was a baby, after telling the health visitor I didn’t vaccinate, she promptly exclaimed, “Oh well, she’s lucky as she has herd immunity from the vaccinated children to protect her!”
She then went on to say that not everyone had the luxury of my decision because if less than 95% of children were vaccinated, then it wouldn’t work anymore. I thought this was a silly concept because if vaccination truly worked, then any child who was vaccinated would be protected from disease, no matter how many ‘infectious’ unvaccinated kids there were, and if the 95% herd immunity figure was a genuine argument, it only points to one thing: the medical profession don’t really believe in the effectiveness of their own vaccines.
What Is The Herd Immunity Theory?
The herd immunity theory was originally coined in 1933 by a researcher called Hedrich. He had been studying measles patterns in the US between 1900-1931 (years before any vaccine was ever invented for measles) and he observed that epidemics of the illness only occurred when less than 68% of children had developed a natural immunity to it. This was based upon the principle that children build their own immunity after suffering with or being exposed to the disease. So the herd immunity theory was, in fact, about natural disease processes and nothing to do with vaccination. If 68% of the population were allowed to build their own natural defences, there would be no raging epidemic.
Later on, vaccinologists adopted the phrase and increased the figure from 68% to 95% with no scientific justification as to why, and then stated that there had to be 95% vaccine coverage to achieve immunity. Essentially, they took Hedrich’s study and manipulated it to promote their vaccination programmes.
(MONTHLY ESTIMATES OF THE CHILD POPULATION “SUSCEPTIBLE’ TO MEASLES, 1900-1931, BALTIMORE, MD, AW HEDRICH, American Journal of Epidemiology, May 1933 – Oxford University Press).
Why Vaccine Induced Herd Immunity is Flawed
If vaccination really immunises, then your vaccinated child will be immunised and therefore protected against any disease an unvaccinated child gets. If he isn’t, his shots didn’t work.
We should also examine whether or not the vaccines actually do provide immunity and in which populations epidemics occurred. Was it the unvaccinated children spreading disease as they would have parents believe? Or were those epidemics already in previously vaccinated people?
To do this I have listed several epidemics that have occurred in the last 100 years or so, including Smallpox, which medics claim that vaccination eradicated.
There was a Smallpox epidemic in Pittsburgh, USA, in 1924. This epidemic was started by a mandatory vaccination campaign in which people were imprisoned if they refused the shot. A health club then started a suit against Dr. Voux, who had headed the vaccination drive, for bringing disease upon the people. Legal council for the health club stated: ‘There have been NO deaths from Smallpox in Pittsburgh during the previous nine years from 1915 to 1924, including the years when there was no vaccination or re-vaccination, at all – and hence, no vaccine immunity.’
They pointed out that the vaccine campaign had caused 22 deaths and 112 cases of vaccine-induced Smallpox. (You can read a detailed history of vaccination in Eleanor McBean’s book, Vaccination Condemned, Better Life Research, 1981).
In Germany between 1947-1974, there were ten outbreaks of Smallpox including 94 people who had been previously ‘immunised’, who then became ill with the disease. (The Vaccination Nonsense, 2004 lectures, Dr. Gerhard Buchwald).
Here are some more recent epidemics in vaccinated populations:
In March 2006, 245 cases of mumps were confirmed in Iowa, US, where the law requires vaccination for school entry. Eleven year-old Will Hean of Davenport was diagnosed with mumps, and his 21 year old sister Kate.Both children had gotten the measles, mumps and rubella vaccine, or MMR. “He had all the shots and everything. You don’t think you’re going to get the mumps after you’ve been inoculated,” said Will’s father, Wayne Hean. (2006, The Associated Press).
In 2002 an outbreak of Varicella (Chickenpox) occurred in a US daycare centre for fully vaccinated children. Varicella developed in 25 of 88 children (28.4 percent) between December 1, 2000, and January 11, 2001. A case occurred in a healthy child who had been vaccinated three years previously and who infected more than 50 percent of his classmates who had no history of varicella. The effectiveness of the vaccine was 44.0 percent against disease of any severity.Children who had been vaccinated three years or more before the outbreak were at greater risk for vaccine failure than those who had been vaccinated more recently.
Conclusions: In this outbreak, vaccination provided poor protection against varicella. Longer interval since vaccination was associated with an increased risk of vaccine failure. Breakthrough infections in vaccinated, healthy persons can be as infectious as varicella in unvaccinated persons. (Outbreak of Varicella at a Day-Care Centre despite Vaccination – 2002 Karin Galil, M.D., M.P.H., Brent Lee, M.D., M.P.H., Tara Strine, M.P.H., Claire Carraher, R.N., Andrew L. Baughman, Ph.D., M.P.H., Melinda Eaton, D.V.M., Jose Montero, M.D., and Jane Seward, M.B., B.S., M.P.H.).
And here’s some vaccine failures for measles:
Five cases of measles secondary vaccine failure with confirmed seroconversion after live measles vaccination. (Scandinavian Journal of Infectious Disease vol. 29, no. 2, 1997, pp.187-90): Two, five, seven and twelve years after vaccination with further attenuated live measles vaccine, three of five patients experienced modified measles infection, and the remaining two had typical measles. “This may be the first SVF case report that confirms the existence of completely waning immunity in recipients of the further attenuated live measles vaccines.”
And Whooping Cough:
Journal of Infectious Diseases, vol. 179, April 1999; 915-923. Temporal trends in the population structure of bordetella pertussis during 1949-1996 in a highly vaccinated population- “Despite the introduction of large-scale pertussis vaccination in 1953 and high vaccination coverage, pertussis is still an endemic disease in The Netherlands, with epidemic outbreaks occurring every 3-5 years.” One factor that might contribute to this is the ability of pertussis strains to adapt to vaccine-induced immunity, causing new strains of pertussis to re-emerge in this well-vaccinated population.
Just recently, Dr. Kari Simonsen, a pediatrician at the University of Nebraska Medical Center, USA, said one in five children who are vaccinated for whooping cough will still get the disease. She said efficacy of the vaccine was ‘comparatively low’, but said ‘It’s the best vaccine we can build to date.’ Despite admitting this, she still believes that parents should get the vaccine for their children.
At St. Robert Bellarmine School in west Omaha, 12 children had confirmed whooping cough, of those, most had been vaccinated.
The Nebraska Department of Health and Human Services reported Thursday that the state has had 117 confirmed cases this year, up from 70 all of last year and 99 in 2006. There were 312 cases in Nebraska in 2005.
In Douglas County, 48 cases have been reported this year. Last year, 21 cases were reported.
This is in a country that gives five doses of the vaccine in the first four years of life and then another dose at 11 years of age!
(Omaha World Herald, ‘Vaccine Didn’t Stop Whooping Cough’, 31st October 2008).
Victor Plotkin – an epidemiologist from Lake County in the US has reported that there have been 82 cases of pertussis in the county so far this year.
‘Plotkin said the county did see very high numbers of cases during a nationwide outbreak of pertussis in 2004 and 2005. In 2004, there were 152 cases of pertussis and 135 cases in 2005. However, before that, pertussis cases in the county had averaged about 8 to 10 a year for many years.
Plotkin said the 2004 and 2005 pertussis outbreak appears that it may have been attributed to waning immunity among older children and adults who had not received booster shots. He said the most recent outbreak is a bit more puzzling because many of the children who are becoming ill are younger children who were recently vaccinated.
“Unfortunately, during this outbreak, even people that have been recently vaccinated are becoming sick anyway,” he said. “Their symptoms are milder, but they still can pass the bacteria along to others and make others sick.”
(Whooping Cough Increases in Lake County – the Vernon Hills Review 20th November 2008).

130 Research papers supporting Vaccine/Autism CausationGinger Taylor, MS
Mainstream research has found that vaccines and their ingredients can cause the underlying medical conditions that committed physicians and researchers are commonly finding in children who have been given an autism diagnosis. These conditions include gastrointestinal damage, immune system impairment, chronic infections, mitochondrial disorders, autoimmune conditions, neurological regression, glial cell activation, brain inflammation, damage to the blood–brain barrier, seizures, synaptic dysfunction, dendritic cell dysfunction, mercury poisoning, aluminum toxicity, gene activation and alteration, glutathione depletion, impaired methylation, oxidative stress, impaired thioredoxin regulation, mineral deficiencies, impairment of the opioid system, endocrine dysfunction, cellular apoptosis, and other disorders

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.

Top Doctors Reveal Vaccines Turn Our Immune System Against Us

Top Doctors Reveal Vaccines Turn Our Immune System Against Us
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.

200 Evidence-Based Reasons NOT To Vaccinate – FREE Research PDF Download!
Quick download here
http://www.greenmedinfo.com/blog/cdn.greenmedinfo.com/sites/default/files/gmipub_58635_anti_therapeutic_action_vaccination_all.pdf
The media, your pediatrician, politicians and health authorities like the CDC and FDA claim that vaccines are safe and effective. So why do hundreds of peer-reviewed studies indicate the opposite is true? Read, download, and share this document widely to provide the necessary evidence-based counterbalance to the pro-vaccination propaganda that has globally infected popular consciousness and discussion like an intractable disease.
It is abundantly clear that if the present-day vaccine climate, namely, that everyone must comply with the CDC’s one-size-fits-all vaccination schedule or be labeled a health risk to society at large, is to succumb to open and balanced discussion, it is the peer-reviewed biomedical evidence itself that is going to pave the way towards making rational debate on the subject happen.
With this aim in mind, GreenMedInfo.com has painstakingly collected over 300 pages of study abstracts culled directly from the National Library of Medicine’s pubmed.gov bibliographic database on the wide-ranging adverse health effects linked to vaccines in the today’s schedule (over 200 distinct adverse effects, including death), as well as numerous studies related to vaccine contamination, and vaccine failure in highly vaccine compliant populations.
This is the literature that the media, politicians and governmental health organizations like the CDC, pretend with abject dishonesty does not exist – as if vaccine injury did not happen, despite the over 3 billion dollars our government has paid out to vaccine injured through the National Vaccine Injury Compensation Fund since it was inaugurated in 1986.
We have written extensively about this research previously, highlighting different studies, focusing on translating their implications to the lay persons (view our vaccine article section here), but we believe that collecting and condensing solely the primary literature itself makes a much more powerful statement.

Study – ‘ASIA’ – autoimmune/inflammatory syndrome induced by adjuvants.
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”.

Measles Transmitted By The Vaccinated, Gov. Researchers Confirm
A remarkable study reveals that a vaccinated individual not only can become infected with measles, but can spread it to others who are also vaccinated against it – doubly disproving two doses of MMR vaccine is “99% effective,” as widely claimed.
One of the fundamental errors in thinking about measles vaccine effectiveness is that receipt of measles-mumps-rubella (MMR) vaccine equates to bona fide immunity against these pathogens. Indeed, it is commonly claimed that receiving two doses of the MMR vaccine is “99 percent effective in preventing measles,”1 despite a voluminous body of contradictory evidence from epidemiology and clinical experience.
This erroneous thinking has led the public, media and government alike to attribute the origin of measles outbreaks, such as the one recently reported at Disney, to the non-vaccinated, even though 18% of the measles cases occurred in those who had been vaccinated against it — hardly the vaccine’s claimed “99% effective.” The vaccine’s obvious fallibility is also indicated by the fact that that the CDC now requires two doses.
But the problems surrounding the failing MMR vaccine go much deeper. First, they carry profound health risks (over 25 of which we have indexed here: MMR vaccine dangers), including increased autism risk, which a senior CDC scientist confessed his agency covered up. Second, not only does the MMR vaccine fail to consistently confer immunity, but those who have been “immunized” with two doses of MMR vaccine can still transmit the infection to others — a phenomena no one is reporting on in the rush to blame the non- or minimally-vaccinated for the outbreak.
MMR Vaccinated Can Still Spread Measles
Last year, a groundbreaking study published in the journal Clinical Infectious Diseases, whose authorship includes scientists working for the Bureau of Immunization, New York City Department of Health and Mental Hygiene, and the National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention (CDC), Atlanta, GA, looked at evidence from the 2011 New York measles outbreak that individuals with prior evidence of measles vaccination and vaccine immunity were both capable of being infected with measles and infecting others with it (secondary transmission).
This finding even aroused the attention of mainstream news reporting, such as this Sciencemag.org article from April 2014 titled “Measles Outbreak Traced to Fully Vaccinated Patient for First Time.”
Titled, “Outbreak of Measles Among Persons With Prior Evidence of Immunity, New York City, 2011,” the groundbreaking study acknowledged that, “Measles may occur in vaccinated individuals, but secondary transmission from such individuals has not been documented.”
In order to find out if measles vaccine compliant individuals are capable of being infected and transmitting the infection to others, they evaluated suspected cases and contacts exposed during a 2011 measles outbreak in NYC. They focused on one patient who had received two doses of measles-containing vaccine and found that,

Study – Predicting post-vaccination autoimmunity: who might be at risk?
Abstract
Vaccinations have been used as an essential tool in the fight against infectious diseases, and succeeded in improving public health. However, adverse effects, including autoimmune conditions may occur following vaccinations (autoimmune/inflammatory syndrome induced by adjuvants–ASIA syndrome). It has been postulated that autoimmunity could be triggered or enhanced by the vaccine immunogen contents, as well as by adjuvants, which are used to increase the immune reaction to the immunogen. Fortunately, vaccination-related ASIA is uncommon. Yet, by defining individuals at risk we may further limit the number of individuals developing post-vaccination ASIA. In this perspective we defined four groups of individuals who might be susceptible to develop vaccination-induced ASIA: patients with prior post-vaccination autoimmune phenomena, patients with a medical history of autoimmunity, patients with a history of allergic reactions, and individuals who are prone to develop autoimmunity (having a family history of autoimmune diseases; asymptomatic carriers of autoantibodies; carrying certain genetic profiles, etc.).

NaturalNews – Top doctors reveal that vaccines can trigger autoimmunity, turning our immune systems against us

Top doctors reveal that vaccines can trigger autoimmunity, turning our immune systems against us
(NaturalNews) Dr. Yehuda Shoenfeld is an Israeli clincian who has been extensively studying the human immune system for more than thirty years. Some say he is at the pinnacle of his profession, and that he is at the core of its foundation. He’s written 25 textbooks on the subject — some of which are key to the backbone of clincial practice. Dr. Shoenfeld has even been referred to as the “Godfather of Autoimmunology.” Autoimmunology is the study of the immune system when it is has turned against itself, resulting in a myriad of conditions including ulcertive colitis, multiple sclerosis and type 1 diabetes.
Lately, Dr. Shoenfeld has been shaking up the world of immunology with evidence that suggests that vaccines may indeed be playing a role in the onset of autoimmune disease. Specifically, some of the star ingredients found in vaccines — like aluminum, a toxic metal — are likely at the helm of the worldwide increase in autoimmune disorders. Evidence supporting this theory has been mounting over the last 15 years, but a noticeably stark increase in research has occured in the last five years. For example, recent study, authored by Dr. Shoenfeld and his colleagues, was published by the journal Pharmacological Research in 2015. In their report, the researchers identified four groups of people who will be most at risk of developing an autoimmune disease following vaccination.
The paper’s authors note that while vaccines may help to prevent illnesses that can cause autoimmunity, “On the other hand, many reports that describe post-vaccination autoimmunity strongly suggest that vaccines can indeed trigger autoimmunity.” The researchers state that “Almost all types of vaccines have been reported to be associated with the onset of ASIA [autoimmune/inflammatory syndrome induced by adjuvants].” The autoimmune diseases that may develop after vaccination include arthritis, lupus (systemic lupus erythematosus, SLE) diabetes mellitus, thrombocytopenia, vasculitis, dermatomyosiositis, Guillain-Barre syndrome and demyelinating disorders. Demyelinating disorders include conditions like multiple sclerosis. Demyelination refers to degradation of the myelin sheath — an insulating material that covers nerves — and results in impaired function of said nerves.
The term ASIA first appeared in the Journal of Autoimmunology a few years ago and is used as an umbrella term to describe a group of similar symptoms that appear after exposure to an adjuvant. Adjuvants are environmental agents, including common vaccine ingredients, that are known to spark the immune system into action. Using ASIA as a model, a massive amount of research has been conducted to begin answering questions surrounding environmental toxins, particularly the metal aluminum used in vaccines, and how they can create an immune system chain reaction in vulnerable individuals, as well as how they can possibly lead to autoimmune disease.
Autoimmune disease is the result of the body’s immune system turning against itself and the human body. When the immune system is functioning normally, it attacks foreign invaders of the body, such as a pathogenic bacteria. In the case of autoimmune disease, however, the immune system has begun attacking the body’s own cells somewhere within the body. In the case of type 1 diabetes, the immune system has targeted the Islets of Langerhans found in the pancreas. In rheumatoid arthritis, the immune system has begun attacking joint tissue. Similar events happen within other autoimmune diseases, but affecting different types of bodily tissues.
Several studies have indicated that the aluminium currently being used in vaccines is a great cause for concern, especially when it comes to autoimmune disease. A 2012 paper authored by researchers from the Neural Dynamics Research Group of the Department of Ophthalmology and Visual Sciences at the University of British Columbia, located in Canada, noted, “According to the US Food and Drug Administration, safety assessments for vaccines have often not included appropriate toxicity studies because vaccines have not been viewed as inherently toxic.”

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
This article is copyrighted by GreenMedInfo LLC, 2015
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.”

Study – Mechanisms of aluminum adjuvant toxicity and autoimmunity in pediatric populations.
Abstract
Immune challenges during early development, including those vaccine-induced, can lead to permanent detrimental alterations of the brain and immune function. Experimental evidence also shows that simultaneous administration of as little as two to three immune adjuvants can overcome genetic resistance to autoimmunity. In some developed countries, by the time children are 4 to 6 years old, they will have received a total of 126 antigenic compounds along with high amounts of aluminum (Al) adjuvants through routine vaccinations. According to the US Food and Drug Administration, safety assessments for vaccines have often not included appropriate toxicity studies because vaccines have not been viewed as inherently toxic. Taken together, these observations raise plausible concerns about the overall safety of current childhood vaccination programs. When assessing adjuvant toxicity in children, several key points ought to be considered: (i) infants and children should not be viewed as “small adults” with regard to toxicological risk as their unique physiology makes them much more vulnerable to toxic insults; (ii) in adult humans Al vaccine adjuvants have been linked to a variety of serious autoimmune and inflammatory conditions (i.e., “ASIA”), yet children are regularly exposed to much higher amounts of Al from vaccines than adults; (iii) it is often assumed that peripheral immune responses do not affect brain function. However, it is now clearly established that there is a bidirectional neuro-immune cross-talk that plays crucial roles in immunoregulation as well as brain function. In turn, perturbations of the neuro-immune axis have been demonstrated in many autoimmune diseases encompassed in “ASIA” and are thought to be driven by a hyperactive immune response; and (iv) the same components of the neuro-immune axis that play key roles in brain development and immune function are heavily targeted by Al adjuvants. In summary, research evidence shows that increasing concerns about current vaccination practices may indeed be warranted. Because children may be most at risk of vaccine-induced complications, a rigorous evaluation of the vaccine-related adverse health impacts in the pediatric population is urgently needed.

Study – Predicting post-vaccination autoimmunity: who might be at risk?
Abstract
Vaccinations have been used as an essential tool in the fight against infectious diseases, and succeeded in improving public health. However, adverse effects, including autoimmune conditions may occur following vaccinations (autoimmune/inflammatory syndrome induced by adjuvants–ASIA syndrome). It has been postulated that autoimmunity could be triggered or enhanced by the vaccine immunogen contents, as well as by adjuvants, which are used to increase the immune reaction to the immunogen. Fortunately, vaccination-related ASIA is uncommon. Yet, by defining individuals at risk we may further limit the number of individuals developing post-vaccination ASIA. In this perspective we defined four groups of individuals who might be susceptible to develop vaccination-induced ASIA: patients with prior post-vaccination autoimmune phenomena, patients with a medical history of autoimmunity, patients with a history of allergic reactions, and individuals who are prone to develop autoimmunity (having a family history of autoimmune diseases; asymptomatic carriers of autoantibodies; carrying certain genetic profiles, etc.).

Study – Vaccines, adjuvants and autoimmunity.
Abstract
Vaccines and autoimmunity are linked fields. Vaccine efficacy is based on whether host immune response against an antigen can elicit a memory T-cell response over time. Although the described side effects thus far have been mostly transient and acute, vaccines are able to elicit the immune system towards an autoimmune reaction. The diagnosis of a definite autoimmune disease and the occurrence of fatal outcome post-vaccination have been less frequently reported. Since vaccines are given to previously healthy hosts, who may have never developed the disease had they not been immunized, adverse events should be carefully accessed and evaluated even if they represent a limited number of occurrences. In this review of the literature, there is evidence of vaccine-induced autoimmunity and adjuvant-induced autoimmunity in both experimental models as well as human patients. Adjuvants and infectious agents may exert their immune-enhancing effects through various functional activities, encompassed by the adjuvant effect. These mechanisms are shared by different conditions triggered by adjuvants leading to the autoimmune/inflammatory syndrome induced by adjuvants (ASIA syndrome). In conclusion, there are several case reports of autoimmune diseases following vaccines, however, due to the limited number of cases, the different classifications of symptoms and the long latency period of the diseases, every attempt for an epidemiological study has so far failed to deliver a connection. Despite this, efforts to unveil the connection between the triggering of the immune system by adjuvants and the development of autoimmune conditions should be undertaken. Vaccinomics is a field that may bring to light novel customized, personalized treatment approaches in the future.

Study – On vaccine’s adjuvants and autoimmunity: Current evidence and future perspectives.
Abstract
Adjuvants are compounds incorporated into vaccines to enhance immunogenicity and the development of these molecules has become an expanding field of research in the last decades. Adding an adjuvant to a vaccine antigen leads to several advantages, including dose sparing and the induction of a more rapid, broader and strong immune response. Several of these molecules have been approved, including aluminium salts, oil-in-water emulsions (MF59, AS03 and AF03), virosomes and AS04. Adjuvants have recently been implicated in the new syndrome named “ASIA-Autoimmune/inflammatory Syndrome Induced by Adjuvants”, which describes an umbrella of clinical conditions including post-vaccination adverse reactions. Recent studies implicate a web of mechanisms in the development of vaccine adjuvant-induced autoimmune diseases, in particular, in those associated with aluminium-based compounds. Fewer and unsystematised data are instead available about other adjuvants, despite recent evidence indicating that vaccines with different adjuvants may also cause specific autoimmune adverse reactions possible towards different pathogenic mechanisms. This topic is of importance as the specific mechanism of action of each single adjuvant may have different effects on the course of different diseases. Herein, we review the current evidence about the mechanism of action of currently employed adjuvants and discuss the mechanisms by which such components may trigger autoimmunity.