Vaccine News – Autism vs. Childhood Diseases: Breaking Down The Walls Of Pro-Vaccine Ignorance

Désirée Röver – Vaccines, Part 1
By OLE DAMMEGARD June 10, 2017
Ole Dammegård interviews Medical Research Journalist Désirée Röver from the Netherlands, about vaccines and the dangers involved. What started her painful journey of discovery into this dark world was the death of her 2 year old son, due to a vaccination.

 

 

Brittney Kara encourages parents to do their research before allowing toxic vaccines to be injected into their children. Start your research by watching Vaccines Revealed featuring 24 vaccine experts by clicking here http://bit.ly/2o0b5Cp and go to http://www.stopmandatoryvaccination.com/personal-choice/ to read Brittney’s vaccine free overview.

“I met with a pediatrician today and she said she watched Vaccines Revealed and she was shocked. She said she looked up the research and it was all there. She said she doesn’t know how to continue her practice as is. She said, should she read the parents the vaccine inserts and let them choose or just cold turkey quit. I hugged her neck and thanked God for opening her eyes.” The free replay is right here . . . tinyurl.com/9Episodes
#RevolutionForChoice #InformedConsent #EducateBeforeYouVaccinate #VAXXED

Medical Doctor who Escaped Vietnam as a Child in the 1970s Explains Why He no Longer Vaccinates
The VAXXED film crew recently interviewed Dr. Anthony Phan in California. Dr. Phan escaped from Vietnam in the 1970s when he was 8 years old. He was separated from his parents and escaped on a fishing boat along with his 2 year old brother.
Making it to the U.S. as a child refugee, Dr. Phan testifies that God led him through college and medical school, and he went on to become a medical doctor at Johns Hopkins.
Dr. Phan talks about how his mentor at Johns Hopkins taught him about the importance of the Hippocratic Oath to “do no harm.”
Do no harm means your oath is to the patient. Not to the CDC, not to the government, not to the FDA, your oath is to the patient.
His mentor also reportedly stated to him:
One day Tony, in your career (this was in 1993), when you see these threesome (CDC, FDA, and the government) in bed together, be very careful. When you see pharmaceutical companies being in bed with the government, and being controlled by the health industry, you need to make a decision about where you want to take your medical career.
Either #1 you retire and get out, because it is back to being controlled again, back to where I escaped (from Vietnam) in 1975.
Dr. Phan explains that his experience with vaccines began in 2000 when he did his fellowship in Integrated Medicine. He was taught to question the practices of “conventional” medicine that are wrong.

 

THOUSANDS protest in numerous cities across Italy in what is now an INTERNATIONAL️ uprising and Revolution for Choice!
What haven’t you been told? Find out now for free: tiny.cc/FreeVaccinationEducation
Networking, exemption information and doctor resources: tinyurl.com/RevolutionForVaccineChoice
Follow us: facebook.com/RevolutionForChoice
#RevolutionForChoice #InformedConsent #EducateBeforeYouVaccinate #VAXXED #Italy #VaccineInjury #NonCompliance #RiseUP

Learn OUR NAMES!!! Our international battle for medical choice and parental choice is only getting started! Join our movement of people who have done their research! . . . Click here to obtain the information you need to make the most informed choices for your yourself and your family >>> tinyurl.com/9Episodes
✴️ Translation courtesy of Teresa Iodice ️
✴️ Networking, exemption information and doctor resources: tinyurl.com/RevolutionForVaccineChoice
✴️ Follow us: facebook.com/RevolutionForChoice
✴️ Read all vaccine inserts: tinyurl.com/ReadTheVaccineInsert
#RevolutionForChoice #InformedConsent #EducateBeforeYouVaccinate #VAXXED #SB277 #RiseUp #Italy #Rome #Naples

Dirty Vaccines: New Study Reveals Prevalence of Contaminants
Posted by Celeste McGovern on Jan 30, 2017 5:31:20 PM
Every Human Vaccine Tested Was Contaminated by Unsafe Levels of Metals and Debris Linked to Cancer and Autoimmune Disease, New Study Reports
Researchers examining 44 samples of 30 different vaccines found dangerous contaminants, including red blood cells in one vaccine and metal toxicants in every single sample tested – except in one animal vaccine.
Using extremely sensitive new technologies not used in vaccine manufacturing, Italian scientists reported they were “baffled” by their discoveries which included single particles and aggregates of organic debris including red cells of human or possibly animal origin and metals including lead, tungsten, gold, and chromium, that have been linked to autoimmune disease and leukemia.
In the study, published this week in the International Journal of Vaccines and Vaccination, the researchers led by Antonietta Gatti, of the National Council of Research of Italy and the Scientific Director of Nanodiagnostics, say their results “show the presence of micro- and nano-sized particulate matter composed of inorganic elements in vaccine samples” not declared in the products’ ingredients lists.
Lead particles were found in the cervical cancer vaccines, Gardasil and Cervarix, for example, and in the seasonal flu vaccine Aggripal manufactured by Novartis as well as in the Meningetec vaccine meant to protect against meningitis C.
Samples of an infant vaccine called Infarix Hexa (against diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis and haemophilus influenzae type B) manufactured by GlaxoSmithKline was found to contain stainless steel, tungsten and a gold-zinc aggregate.
Other metal contaminants included platinum, silver, bismuth, iron, and chromium. Chromium (alone or in alloy with iron and nickel) was identified in 25 of the human vaccines from Italy and France that were tested.
GSK’s Fluarix vaccine for children three years and older contained 11 metals and aggregates of metals. Similar aggregates to those identified in the vaccines have been shown to be prevalent in cases of leukemia, the researchers noted.

If a parent is vaccinating their child, these are just some facts they need to understand.
Greg Wyatt·Tuesday, June 20, 2017
“If a parent is vaccinating their child, these are just some facts they need to understand.

1. I understand that the pharmaceutical company who made this vaccine has NO liability if it injures or kills my child.
2. If my child is killed or hurt by a vaccine, the public will pay through increased taxes for any damage the vaccine does and in Canada it’s very little payment for a dead or injured child.
3. I understand that these vaccines contains neurotoxins such as aluminum and mercury that far exceed “safe levels” deemed by the EPA.
4. I understand that these vaccines contain carcinogenic ingredients PROVEN to cause CANCER.
5. I understand that some vaccines are made from aborted fetal cell lines, of both humans and animals and their DNA is INJECTED into you and your child along with everything else (including an adjuvant that tells your immune system to attack EVERYTHING in the vaccine, INCLUDING HUMAN CELLS.)
6. I understand that getting this vaccine does not ensure that I will be protected from the disease. Many OUTBREAKS include a Population of 100% vaccinated individuals.

Patients with an Allergy to Eggs Are at Risk of Anaphylaxis from MMR Vaccine
Posted on: Wednesday, February 1st 2017 at 10:30 am
Written By: Christina England, BA Hons
According to the National Institute of Allergy and Infectious Diseases Patients with an Allergy to Eggs Are at Risk of Anaphylaxis if Vaccinated with the MMR!
It is estimated that up to 15 million US citizens are currently suffering from food allergies. In 2013, a paper published on the CDC website stated that between 1997 and 2011, the prevalence of food and skin allergies increased in children under age of 18. This is extremely worrying, as according to the Food Allergy Research & Education website, a food allergy sends someone to the emergency department every three minutes, which, according to them, amounts to approximately 200,000 visits to the ER every year.
The NIAID Recommend the MMR to Children with Egg Allergies
In 2010, the National Institute of Allergy and Infectious Diseases (NIAID) published a paper titled Guidelines for the Diagnosis and Management of Food Allergy in the United States. The paper described how the NIAID had joined forces with 30 professional organizations, federal agencies and patient advocacy groups to set guidelines for the management and safety of patients suffering from food allergies.
One of the sections highlighted was a section titled Vaccinations in Patients with Egg Allergies.’ The authors wrote:
“In Summary: Patients who have generated IgE antibodies to an allergen are at risk for anaphylaxis with systemic exposure to that allergen. Thus, patients who have IgE-mediated egg allergy are at risk for anaphylaxis if injected with vaccines containing egg 17 protein.” (own emphasis)
They continued:
“More detailed information about specific egg-containing vaccines (measles, mumps, and rubella [MMR], MMR with varicella [MMRV], influenza, yellow fever, and rabies) is provided in … the Guidelines.
The EP recognizes that changes in these recommendations may occur in the future as there is an increased understanding of the risk factors for allergic reactions and as vaccine manufacturing processes improve and decrease the final egg protein content of vaccines. For the most current recommendations, health care professionals should refer to the Web sites of the American Academy of Pediatrics (AAP) and Advisory Committee for Immunization Practices (ACIP):
http://aapredbook.aappublications.org/
http://www.cdc.gov/vaccines/recs/acip/
However, despite stating that patients who have an allergy to eggs are at risk of anaphylaxis if they receive a vaccine containing the egg 17 protein, it appears that they are recommending the vaccine anyway.
I say this, because in section 5.1.11.1 they stated:
“Measles, Mumps, Rubella, and Varicella Vaccine
Guideline 31: The EP recognizes the varying consensus recommendations of the different organizations on this particular vaccine and recommends that children with egg allergy, even those with a history of severe reactions, receive vaccines for MMR and MMRV. The safety of this practice has been recognized by ACIP and AAP and is noted in the approved product prescribing information for these vaccines.” (own emphasis)
What I found interesting was the fact that the NIAID did not apply the same guidelines to any of the other vaccinations listed.
In fact, their recommendations for the flu vaccine clearly stated:
“In Summary: The EP concludes that insufficient evidence exists to recommend administering influenza vaccine, either inactivated or live-attenuated, to patients with a history of severe reactions to egg proteins. Severe reactions include a history of hives, angioedema, allergic asthma, or systemic anaphylaxis to egg proteins (or chicken proteins). Less severe or local manifestations of allergy to egg or feathers are not contraindications. However, the EP notes that egg allergy is relatively common among the very patients who would highly benefit from influenza vaccination. Such patients include children and young adults (from 6 months to 18 years old for seasonal influenza, and from 6 months to 24 years old for H1N1 influenza) and all patients with asthma. It should be noted that live-attenuated vaccine is not licensed for use in patients with asthma.” (own emphasis)
They continued:
“Although ACIP and AAP, and also the vaccine manufacturers, do not recommend influenza vaccination in patients who are allergic to egg, several publications have described different approaches to giving the influenza vaccine to patients with severe allergic reactions to egg. These approaches, which depend on the ovalbumin content and the results of SPTs or intradermal tests with the vaccine, include a single dose of vaccine, two doses of vaccine, or multiple doses. However, the evidence supporting these approaches is limited by the small numbers of patients included in each study. Moreover, data indicate that, although the vaccines are relatively safe, there remains some, albeit low, risk of systemic reactions. Also, negative SPT results do not accurately predict safety of vaccination, in that 5 percent of patients with negative SPTs had systemic reactions to vaccination.” (own emphasis)
With these recommendations in mind, we need to ask ourselves how many of our doctors are fully aware of any of these guidelines? If they are aware of this information, why are so many doctors not adhering to them?

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

Autism vs. Childhood Diseases: Breaking Down The Walls Of Pro-Vaccine Ignorance
By Tami Canal On June 19, 2017
I can’t tell you how absolutely fed up I am with tragically misinformed people who proclaim that they would prefer to have an autistic child versus one with a case of the measles, mumps, chicken pox, etc.
A comment like that demonstrates immense ignorance in regards to the LIFETIME of issues that autism presents–things like social dysfunction, the inability to speak, aggression, self-destructive behavior, and a staggeringly diminished life expectancy. If you are one of the people who have ever believed measles or other infectious diseases to be worse than autism, this is for you.
Let’s take a look and examine these so-called “deadly” childhood diseases.

1. Chicken Pox (Varicella) = itchy rash with small fluid-filled blisters; 5-7 days of feeling tired and sluggish; mild fever; decreased appetite. Resolves itself.
2. Diptheria = low fever, sore throat, croup-like cough; many infections are asymptomatic or mild. Treat with antitoxin and antibiotics. Garlic juice and table salt are natural remedies to successfully treat diphtheria, as well.
3. Haemophilus influenzae Type B (Hib) = flu symptoms, stiff neck, lethargy. Treat with antibiotics for 10 days.
4. Hepatitis A = transmitted by eating food or drinking water contaminated with feces; children usually have no symptoms; when symptoms occur, they include flu-like symptoms, nausea, jaundice. Resolves itself.
5. Hepatitis B = transmitted through blood, semen, vaginal fluids; flu-like symptoms, dark urine, vomiting, jaundice; most people do not show symptoms. Acute Hep B resolves itself.
6. Human Papilloma Virus (HPV) = transmitted sexually; usually resolves itself with no symptoms; takes years to develop into cancer; regular pap screens prevent cancer; vaccine discontinued in Japan due to adverse reactions.
7. Influenza (flu) = high fever, cold symptoms, vomiting; lasts 7-10 days; Resolves itself. (Flu vaccine contains mercury [thimerosal]).
8. Measles = fever, cold symptoms, rash; 7-10 days; Resolves itself. Infection can be avoided with proper nutrition, primarily adequate levels of Vitamin A and C.
9. Meningitis = flu symptoms, stiff neck; usually caused by bacteria or virus; viral usually causes no symptoms and resolves itself; bacterial is spread through saliva (kissing, coughing); Most people who ‘carry’ the bacteria never become sick; bacterial meningitis is treated with antibiotics.
10. Mumps = fever, swelling of salivary glands; many people show no symptoms; Resolves itself within a few weeks. (There are many effective natural home remedies for mumps which are safe and provide relief from pain without any harmful side effects.)
11. Pertussis (whooping cough) = dry cough, watery eyes, slight fever, lethargy; treated with high doses of vitamin C; garlic, almond oil, honey, and onion are also effective, natural remedies to treat pertussis.
12. Pneumococcal Pneumonia = flu-like symptoms, fatigue, chills, stiff neck; Treated with antibiotics.
13. Poliomyelitis = 72% of infections cause no symptoms; 25% flu-like symptoms that last 2-5 days; 0.5% leads to more severe symptoms such as paralytic polio; only people with the paralytic infection are considered to have the disease. It is noteworthy to mention that a congressional hearing in the 1950s shed light that polio was actually the result of DDT poisoning and that the federal government and the chemical industry fabricated polio to conceal the true cause of paralysis-inducing epidemic sweeping the country. (Read more about polio here.)
14. Rotavirus = infection in the intestinal tract that causes vomiting, diarrhea, and dehydration; Children, even those that are vaccinated for rotavirus, may develop the disease more than once. A diet high in potassium, such as BRAT, will help bind the bowels and can greatly alleviate the symptoms of Rotavirus. Other natural remedies can be found here.
15. Rubella (German measles) = flu-like symptoms, swollen lymph nodes, joint pain, fatigue, rash; 1-3 days; 25 to 50% of people infected with rubella will not experience any symptoms. Resolves itself. Turmeric, licorice, and citrus are highly effective home remedies.
16. Tetanus = sudden, painful contractions of muscle groups; caused by Clostridium tetani transmitted through broken skin; Prevention is to allow wound to bleed freely. Tetanus bacteria is anaerobic – meaning oxygen will kill it.

Dr. Andrew Moulden: Every Vaccine Produces Microvascular Damage
by John P. Thomas
Health Impact News
Dr. Andrew Moulden recognized that every dose of vaccine given to a person produced microvascular damage whether or not the person was aware of the damage or had debilitating symptoms at the time the vaccines were given. He courageously stepped out of the conventional box of medical diagnosis and treatment, and gave us a new way to look at modern neurodevelopmental illnesses and syndromes.
This series of articles is intended to preserve the work of Dr. Moulden, who unexpectedly died in November of 2013. I want to acknowledge the contribution of this forward-thinking pioneer who worked to explain the truth about vaccine damage. This is article two in a series of four articles about Dr. Moulden’s life work.
As a physician and PhD researcher, he raised strong public objection to vaccine use, because he could literally see evidence of vaccine damage in the expressions of the human face. Each dose of a vaccine causes tiny strokes in the brain and in other organs of the body, which bring about a wide range of unexpected health conditions.
Dr. Moulden saw that the rapid rise in modern neurodevelopmental diseases such as autism, Alzheimer’s, and numerous other syndromes were actually caused by the same process. He saw the current epidemic of these modern diseases as having a single origin. The notion of single diseases with single causes had to be put aside, because that model could not adequately explain what we are facing in the world today.
How Vaccines and Toxins Producing a Syndrome of Closely Related Illnesses
Dr. Moulden understood that vaccines and toxins (in the air, in our water, in our homes, and in our food) were producing a syndrome of closely related illnesses. He said that it was time to begin thinking in terms of multiple causes for a syndrome that had multiple sets of symptoms.
Multiple factors can work together to trigger a single type of reaction in the body, which can then produce various sets of symptoms. Even though there were different sets of symptoms and different disease names given to each one, they were actually all part of a spectrum of diseases that he called Moulden Anoxia Spectrum Syndromes.
Learning disabilities, autism, Alzheimer’s, irritable bowel disease, Crohn’s disease, colitis, food allergies, shaken baby syndrome, sudden infant death, idiopathic seizure disorders, Gulf War syndrome, Gardasil adverse reactions, schizophrenia, Tourette’s syndrome, chronic fatigue syndrome, fibromyalgia, expressive aphasia, impaired speech skills, attention deficit disorders, silent ischemic strokes, blood clots, idiopathic thrombocytopenia purpura, Parkinson’s disease, and other modern neurodevelopmental disorders are closely related in many ways, and are part of a larger syndrome.

Slate.com tries to school Trump on vaccines. Fails.
You should watch this hilarious takedown of a Slate.com article on Trump and his Slow-Vaxxin’ ways.
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Study – Oxidative Stress and NAD+ in Ischemic Brain Injury: Current Advances and Future Perspectives
Abstract
Numerous studies have indicated oxidative stress as a key pathological factor in ischemic brain injury. One of the key links between oxidative stress and cell death is excessive activation of poly(ADP-ribose) polymerase-1 (PARP-1), which plays an important role in the ischemic brain damage in male animals. Multiple studies have also suggested that NAD+ depletion mediates PARP-1 cytotoxicity, and NAD+ administration can decrease ischemic brain injury.
A number of recent studies have provided novel information regarding the mechanisms underlying the roles of oxidative stress and NAD+-dependent enzymes in ischemic brain injury. Of particular interest, there have been exciting progresses regarding the mechanisms underlying the roles of NADPH oxidase and PARP-1 in cerebral ischemia. For examples, it has been suggested that androgen signaling and binding of PARP-1 onto estrogen receptors could account for the intriguing findings that PARP-1 plays remarkably differential roles in the ischemic brain damage of male and female animals; and some studies have suggested casein kinase 2, copper-zinc superoxide dismutase, and estrogen signaling can modulate the expression and activity of NADPH oxidase.
This review summarizes these important current advances, and proposes future perspectives for the studies on the roles of oxidative stress and NAD+ in cerebral ischemia. It is increasingly likely that future studies on NAD- and NADP-dependent enzymes, such as NADPH oxidase, PARP-1, and sirtuins, would expose novel mechanisms underlying the roles of oxidative stress in cerebral ischemia, and suggest new therapeutic strategies for treating the debilitating disease.

Natural News – Gardasil, considered the most dangerous vaccine on the market, may soon be pushed for infants
Wednesday, November 23, 2016 by: Vicki Batts
(NaturalNews) Gardasil has been the subject of controversy for many years now. In fact, it has even been regarded as one of the most dangerous vaccines on the market today. Perhaps what is most alarming about this treacherous vaccine, however, is the fact that its manufacturer, Merck & Co, now wants to begin marketing their product to infants – and trials on babies have already begun. Merck recently launched a Gardasil vaccine trial on children at least one year old, and it’s set to conclude in early 2017.
You read that right. A pharmaceutical giant is testing a vaccine for an STD on babies. It doesn’t really get more corrupt and outrageous than that, now does it?
Gardasil was developed for the STD known as HPV, and was approved by the FDA in 2006. The disease did not become of concern until the 1980s, when research first suggested that there may be a link between HPV and cervical cancer. However, whether this link actually exists has been a major point of contention. There are several hypotheses that explain why HPV may not actually cause cancer, but one particularly interesting theory was expressed by McCormack et al in their paper published by the journal Molecular Cytogenetics in 2015. The research team also raised several significant questions about the prevailing theory on the connection between HPV and cervical cancer. For example, HPV is present in 70 to 80 percent of the American adult population, so why does cervical cancer only effect one out of ever 10,000 women?
According to their paper, neither HPV nor genetic predisposition is required for the onset of cervical cancer. In fact, all of the cervical cancer cells analyzed during the course of their study contained new abnormal karyotypes. The genetic makeup of these new abnormal karyotypes suggested that the cervical cancers originated within the karyotypes, and not from a virus. A karyotype is the size, number and shape of chromosomes within an organism. Their theory, called the Karyotypic Speciation Theory, essentially suggests that “carcinomas are generated de novo from cellular chromosomes, genes and proteins, which are not immunogenic in the host of origin (just like all other cancers).” As SaneVax.org explains, in this theory, hypothetical cancer cells that are generated by viral proteins (such as HPV) would be eliminated by antiviral immunity.

Dr Tenpenny on Vit K
TinyURL.com/TenpennyVitK
#VaXism NEWS

VACCINURILE ȘI AUTOIMUNITATEA – un tratat de imunologie aplicată echilibrat; rezultatul zecilor de ani de experiență în vaccinologie și autoimunitate și a studierii unei cazuistici și literaturi de specialitate extrem de vaste, are 37 de capitole și exprimă un adevăr dramatic: o parte dintre oamenii sănătoși (despre care nu știm dacă s-ar fi îmbolnăvit vreodată) fac boli autoimune după și prin administrarea unui vaccin: lupus, vasculite, artrită reumatoidă, boli de țesut conjunctiv nediferențiate, purpură trombocitopenică, boală celiacă ETC.
« Autorii cărții sunt medici specializați în imunologie fundamentală și clinică. Este vorba de o lucrare curajoasă în condițiile vremurilor noastre deoarece trezește un spirit de prudență – altfel destul de amorțit sau bine manipulat – spirit prevazător imperios necesar de vreme ce unele guverne vor să decreteze obligativitatea vaccinării, adică să-și agreseze poporul lor cu o lege totalitară. », Dr. Pavel Chirilă, Prefață la ediția 2016.

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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.