A study published in the Journal of Toxicology and Environmental Health determined that mercury exposure can induce immune, sensory, neurological, motor and behavioural dysfunctions similar to traits defining or associated with ASDs. Based upon differential diagnoses, 8 of 9 patients examined were exposed to significant mercury from Thimerosal-containing vaccine preparations during their fetal/infant developmental periods. These previously normal developing children suffered mercury encephalopathies that manifested with clinical symptoms consistent with regressive ASDs. Evidence for mercury intoxication should be considered in the differential diagnosis as contributing to some regressive ASDs.
US National Library of Medicine
National Institutes of Health – May 2007
Geier DA, Geier MR.
Author information
Institute of Chronic Illnesses, Inc., Silver Spring, Maryland, USA.
Abstract
Impairments in social relatedness and communication, repetitive behaviors, and stereotypic abnormal movement patterns characterize autism spectrum disorders (ASDs). It is clear that while genetic factors are important to the pathogenesis of ASDs, mercury exposure can induce immune, sensory, neurological, motor, and behavioral dysfunctions similar to traits defining or associated with ASDs. The Institutional Review Board of the Institute for Chronic Illnesses (Office for Human Research Protections, U.S. Department of Health and Human Services, IRB number IRB00005375) approved the present study. A case series of nine patients who presented to the Genetic Centers of America for a genetic/developmental evaluation are discussed. Eight of nine patients (one patient was found to have an ASD due to Rett’s syndrome) (a) had regressive ASDs; (b) had elevated levels of androgens; (c) excreted significant amounts of mercury post chelation challenge; (d) had biochemical evidence of decreased function in their glutathione pathways; (e) had no known significant mercury exposure except from Thimerosal-containing vaccines/Rho(D)-immune globulin preparations; and (f) had alternate causes for their regressive ASDs ruled out. There was a significant dose-response relationship between the severity of the regressive ASDs observed and the total mercury dose children received from Thimerosal-containing vaccines/Rho (D)-immune globulin preparations. Based upon differential diagnoses, 8 of 9 patients examined were exposed to significant mercury from Thimerosal-containing biologic/vaccine preparations during their fetal/infant developmental periods, and subsequently, between 12 and 24 mo of age, these previously normally developing children suffered mercury toxic encephalopathies that manifested with clinical symptoms consistent with regressive ASDs. Evidence for mercury intoxication should be considered in the differential diagnosis as contributing to some regressive ASDs.
A study conducted by the Department of Obstetrics and Gynaecology at University of Pittsburgh’s School of Medicine showed that Macaques are commonly used in pre-clinical vaccine safety testing. Collective Evolution does not support animals testing, we feel there is a large amount of evidence and research that already indicated the links to vaccines in which some animals have been used to illustrate. The objective of this study was to compare early infant cognition and behaviour with amygdala size and opioid binding in rhesus macaques receiving the recommended childhood vaccines. The animal model, which examines for the first time, behavioural, functional and neuromorphometric consequences of the childhood vaccine regimen, mimics certain neurological abnormalities of autism. These findings raise important safety issues while providing a potential model for examining aspects of causation and disease pathogenesis in acquired disorders of behaviour and development.
Author information
Laura Hewitson – 1,2,*, Brian J. Lopresti – 3, Carol Stott – 4, N. Scott Mason – 3 and Jaime Tomko – 1
1 Department of Obstetrics and Gynecology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA;
2 Thoughtful House Center for Children, Austin, TX, USA;
3 Department of Radiology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA;
4 Independent Chartered Scientist, Cambridge, UK;
Abstract
This longitudinal, case-control pilot study examined amygdala growth in rhesus macaque infants receiving the complete US childhood vaccine schedule (1994-1999). Longitudinal structural and functional neuroimaging was undertaken to examine central effects of the vaccine regimen on the developing brain. Vaccine-exposed and saline-injected control infants underwent MRI and PET imaging at approximately 4 and 6 months of age, representing two specific timeframes within the vaccination schedule. Volumetric analyses showed that exposed animals did not undergo the maturational changes over time in amygdala volume that was observed in unexposed animals. After controlling for left amygdala volume, the binding of the opioid antagonist [11C]diprenorphine (DPN) in exposed animals remained relatively constant over time, compared with unexposed animals, in which a significant decrease in [11C]DPN binding occurred. These results suggest that maturational changes in amygdala volume and the binding capacity of [11C]DPN in the amygdala was significantly altered in infant macaques receiving the vaccine schedule. The macaque infant is a relevant animal model in which to investigate specific environmental exposures and structural/functional neuroimaging during neurodevelopment.
A study conducted by The George Washington University School of Public Health from the Department of Epidemiology and Biostatistics determined that significantly increased rate ratios were observed for autism and autism spectrum disorders as a result of exposure to mercury from Thimerosal-containing vaccines.
US National Library of Medicine
National Institutes of Health – Aug 2008
Young HA, Geier DA, Geier MR.
Author information
The George Washington University School of Public Health and Health Services, Department of Epidemiology and Biostatistics, United States.
Abstract
The study evaluated possible associations between neurodevelopmental disorders (NDs) and exposure to mercury (Hg) from Thimerosal-containing vaccines (TCVs) by examining the automated Vaccine Safety Datalink (VSD). A total of 278,624 subjects were identified in birth cohorts from 1990-1996 that had received their first oral polio vaccination by 3 months of age in the VSD. The birth cohort prevalence rate of medically diagnosed International Classification of Disease, 9th revision (ICD-9) specific NDs and control outcomes were calculated. Exposures to Hg from TCVs were calculated by birth cohort for specific exposure windows from birth-7 months and birth-13 months of age. Poisson regression analysis was used to model the association between the prevalence of outcomes and Hg doses from TCVs. Consistent significantly increased rate ratios were observed for autism, autism spectrum disorders, tics, attention deficit disorder, and emotional disturbances with Hg exposure from TCVs. By contrast, none of the control outcomes had significantly increased rate ratios with Hg exposure from TCVs. Routine childhood vaccination should be continued to help reduce the morbidity and mortality associated with infectious diseases, but efforts should be undertaken to remove Hg from vaccines. Additional studies should be conducted to further evaluate the relationship between Hg exposure and NDs.
VAXXED TV – My Vaxxed child versus my unvaccinated child
1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
Study published in the Annals of Clinical Psychiatry suggests that Autism is likely triggered by a virus, and that measles virus (MV and/or MMR vaccine) might be a very good candidate. It supports the hypothesis that a virus-dincued autoimmune response may play a causal role in autism.
US National Library of Medicine
National Institutes of Health – 2002
Singh VK, Lin SX, Newell E, Nelson C.
Author information
Department of Biology and Biotechnology Center, Utah State University, Logan, Utah 84322, USA. singhvk@cc.usu.edu
Abstract
Autoimmunity to the central nervous system (CNS), especially to myelin basic protein (MBP), may play a causal role in autism, a neurodevelopmental disorder. Because many autistic children harbor elevated levels of measles antibodies, we conducted a serological study of measles-mumps-rubella (MMR) and MBP autoantibodies. Using serum samples of 125 autistic children and 92 control children, antibodies were assayed by ELISA or immunoblotting methods. ELISA analysis showed a significant increase in the level of MMR antibodies in autistic children. Immunoblotting analysis revealed the presence of an unusual MMR antibody in 75 of 125 (60%) autistic sera but not in control sera. This antibody specifically detected a protein of 73-75 kD of MMR. This protein band, as analyzed with monoclonal antibodies, was immunopositive for measles hemagglutinin (HA) protein but not for measles nucleoprotein and rubella or mumps viral proteins. Thus the MMR antibody in autistic sera detected measles HA protein, which is unique to the measles subunit of the vaccine. Furthermore, over 90% of MMR antibody-positive autistic sera were also positive for MBP autoantibodies, suggesting a strong association between MMR and CNS autoimmunity in autism. Stemming from this evidence, we suggest that an inappropriate antibody response to MMR, specifically the measles component thereof, might be related to pathogenesis of autism.
A study published in the American Journal of Clinical Nutrition determined that an increased vulnerability to oxidative stress and decreased capacity for methylation may contribute to the development and clinical manifestation of autism. It’s well known that viral infections cause increased oxidative stress. Research suggests that metals, including those found in many vaccines are directly involved in increasing oxidative stress.
S Jill James, Paul Cutler, Stepan Melnyk, Stefanie Jernigan, Laurette Janak, David W Gaylor, and James A Neubrander
Author Affiliations
From the Department of Pediatrics, University of Arkansas for Medical Sciences, and the Arkansas Children’s Hospital Research Institute, Little Rock, AR (SJJ, SM, and SJ); Niagara Falls, NY (PC); Colden, NY (LJ); Gaylor and Associates, LLC, Eureka Springs, AR (DWG); and Edison, NJ (JAN)
Abstract
Background: Autism is a complex neurodevelopmental disorder that usually presents in early childhood and that is thought to be influenced by genetic and environmental factors. Although abnormal metabolism of methionine and homocysteine has been associated with other neurologic diseases, these pathways have not been evaluated in persons with autism.
Objective: The purpose of this study was to evaluate plasma concentrations of metabolites in the methionine transmethylation and transsulfuration pathways in children diagnosed with autism.
Design: Plasma concentrations of methionine, S-adenosylmethionine (SAM), S-adenosylhomocysteine (SAH), adenosine, homocysteine, cystathionine, cysteine, and oxidized and reduced glutathione were measured in 20 children with autism and in 33 control children. On the basis of the abnormal metabolic profile, a targeted nutritional intervention trial with folinic acid, betaine, and methylcobalamin was initiated in a subset of the autistic children.
Results: Relative to the control children, the children with autism had significantly lower baseline plasma concentrations of methionine, SAM, homocysteine, cystathionine, cysteine, and total glutathione and significantly higher concentrations of SAH, adenosine, and oxidized glutathione. This metabolic profile is consistent with impaired capacity for methylation (significantly lower ratio of SAM to SAH) and increased oxidative stress (significantly lower redox ratio of reduced glutathione to oxidized glutathione) in children with autism. The intervention trial was effective in normalizing the metabolic imbalance in the autistic children.
Conclusions: An increased vulnerability to oxidative stress and a decreased capacity for methylation may contribute to the development and clinical manifestation of autism.
A study published by the Department of Pharmaceutical Sciences at Northeastern University, Boston determined that a novel growth factor signalling pathway that regulates methionine synthase(MS) activity and thereby modulates methylation reactions. The potent inhibition of this pathway by ethanol, lead, mercury, aluminum and thimerosal suggests that it may be an important target of neurodevelopmental toxins. You can read more about this here, and here. You can read more about the MS/autism link here
US National Library of Medicine
National Institutes of Health – Apr 2004
Waly M, Olteanu H, Banerjee R, Choi SW, Mason JB, Parker BS, Sukumar S, Shim S, Sharma A, Benzecry JM, Power-Charnitsky VA, Deth RC.
Author information
Department of Pharmaceutical Sciences, Northeastern University, Boston, MA 02115, USA.
Abstract
Methylation events play a critical role in the ability of growth factors to promote normal development. Neurodevelopmental toxins, such as ethanol and heavy metals, interrupt growth factor signaling, raising the possibility that they might exert adverse effects on methylation. We found that insulin-like growth factor-1 (IGF-1)- and dopamine-stimulated methionine synthase (MS) activity and folate-dependent methylation of phospholipids in SH-SY5Y human neuroblastoma cells, via a PI3-kinase- and MAP-kinase-dependent mechanism. The stimulation of this pathway increased DNA methylation, while its inhibition increased methylation-sensitive gene expression. Ethanol potently interfered with IGF-1 activation of MS and blocked its effect on DNA methylation, whereas it did not inhibit the effects of dopamine. Metal ions potently affected IGF-1 and dopamine-stimulated MS activity, as well as folate-dependent phospholipid methylation: Cu(2+) promoted enzyme activity and methylation, while Cu(+), Pb(2+), Hg(2+) and Al(3+) were inhibitory. The ethylmercury-containing preservative thimerosal inhibited both IGF-1- and dopamine-stimulated methylation with an IC(50) of 1 nM and eliminated MS activity. Our findings outline a novel growth factor signaling pathway that regulates MS activity and thereby modulates methylation reactions, including DNA methylation. The potent inhibition of this pathway by ethanol, lead, mercury, aluminum and thimerosal suggests that it may be an important target of neurodevelopmental toxins.
VAXXED TV – Vaccines gave my son autism
Vaccines while pregnant injured my daughter
Dr. Suzanne Humphries discusses smallpox from 1797 – 2005
MERCK’S DIRTY LITTLE SECRET – BY DR. SUZANNE HUMPHRIES
1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
Dr. Andrew Moulden: Every Vaccine Produces Harm
by John P. Thomas
Health Impact News
Canadian physician Dr. Andrew Moulden provided clear scientific evidence to prove that every dose of vaccine given to a child or an adult produces harm. The truth that he uncovered was rejected by the conventional medical system and the pharmaceutical industry. Nevertheless, his warning and his message to America remains as a solid legacy of the man who stood up against big pharma and their program to vaccinate every person on the Earth.
Dr Moulden died unexpectedly in November of 2013 at age 49.
Because of the strong opposition from big pharma concerning Dr. Moulden’s research, I became concerned that the name of this brilliant researcher and his life’s work had nearly been deleted from the internet. His reputation was being disparaged, and his message of warning and hope was being distorted and buried without a tombstone.
I prepared a series of articles as a tribute to a great physician and as a memorial to a courageous individual who was not afraid to speak the truth about medical corruption and a flawed healthcare system that does more to harm health than it does to cure disease.
This is the first in a series of four articles about Dr. Moulden — the man, the physician, and the powerful advocate for ending all vaccine use. In future articles, I will summarize his detailed scientific evidence, which shows how vaccine damage occurs. I will explain the common mechanisms behind vaccine damage and how vaccines harm the health of everyone who receives them regardless of whether or not they notice any adverse reactions at the time they take the shots.
Dr. Moulden stated:
What we have done to each other [with vaccines] has produced the most profound damage to humankind by humankind in the history of humanity. And the reason why we got here is partly because of:
Our arrogance in thinking that we know everything. In physiology and medicine we do not know everything!
[Our greed] to advance our own self-interest to make money, to sell products and to advance corporate alliances. Commercialization has overtaken the fundamental human value of “do unto others as you would have others do unto you.” When society turns toward this human value, then we would all be working together for the greater good of each other. [However, other values have become more important] I don’t care whose feet I step on or how I get there as long as my American dream is realized. I don’t care who has to pay for it on the way of getting there. [1]
Dr. Moulden’s Credibility
Was Dr. Moulden a crackpot as some sources claim, or was he a brilliant physician and researcher? This series of articles will set the record straight, and summarize the contribution that his work has made to medical knowledge.
When I evaluate the credibility of people who are unknown to me, I begin by seeking answers to a few basic questions. For example: Is this person offering opinion, or can he or she back up the claims with valid science? Does he have educational credentials? Are there other physicians and scientists who support his or her beliefs and recommendations? Is this person controlled by the pharmaceutical industry, allopathic medical associations, or the US FDA (US Food and Drug Administration)? And finally, what do Quackwatch and their friends have to say about the person?
Dr. Moulden had a PhD in Clinical Psychology and Neuropsychology. He had a master’s degree in child development, and was also a medical doctor. [2] His work was respected by other researchers who don’t march to the drumbeat of the pharmaceutical companies. Dr. Moulden was a threat to the pharmaceutical industry, and their Quackwatch family of 21 related websites treated him as an enemy. [3, 4]
Vaccine Contraindications: Six People Who Should Not Be Vaccinated
The debate surrounding vaccinations is a fierce one, and personally, I don’t like to argue about it. I’m happy to make the right choices for my family while you make the right ones for yours. (I personally have suffered adverse reactions to vaccinations.) It’s ok to have different opinions, really it is. But there are a lot of folks out there who think everyone should be vaccinated, period, and those who choose not to vaccinate should be penalized or worse.
Listen. I get that people are scared and there’s a lot of fear-mongering in the media. But let’s be realistic here: vaccinations are a medical procedure. There are risks. Vaccinations are not right for everyone. There are at least six types of people in particular who should avoid vaccinations, and below, I’ll spell it out.
Vaccine Contraindications
Just like a particular surgery or prescription medication won’t work well for everyone, vaccinations are not a good choice for everyone.
Some people, in particular, are much more likely to have adverse reactions to vaccinations, including:
– Those with an autoimmune disease
– Children born to a mother with an autoimmune disease
– Anyone who is sick
– Pregnant women
– Those who have previously had a reaction to a vaccination
One size does not fit all
Clearly, vaccinations are not the right choice for everyone, and each family should decide what is right for them and their children. When parents are aware of vaccine contraindications, they can make informed and safer choices for their children.
Please share this post so that other parents can learn about vaccine contraindications and decide if vaccination is right for their children.
USA: Highest Vaccination Rate in the World Has the Worst Health
by PAUL FASSA
That “worst health” label includes a ranking of 34th in the world with infant mortality. In other words, the USA has the 34th worst infant survival with its highest rate of vaccinations. Some are directly from multiple vaccinations administered.
But the USA leads the world in infant vaccinations, those administered during the first year after their births – 26 vaccinations during that time.
The only vaccination I recall receiving during early childhood, circa 1948, was the smallpox vaccine, the one that left a circle of shallow pockmarks on the upper arm, a non-ink tattoo that proved you had received that vaccine. Months later there was the booster shot which gave me a vacation of several days away from my first grade teacher while sitting out the chicken pox.
During Naval training the mass vaccination high pressure hand held gun that replaced syringes and needles was tried on us with the polio shot. I wound up with a vacation in the base infirmary with an extended period of the flu. Between those two, there may have been a tetanus shot or two.
From the Healthy Home Economist:
-In1950, there were 3 childhood vaccines typically given when a child entered school.
-In 1983, there were 10 recommended vaccines by the age of 6 years old (24 doses, 7 injections, 4 oral doses for polio).
-In 2010, the CDC vax schedule totaled 68 doses with more than half given by the time a child was only a year and a half old.
-In 2016, the schedule has increased to 74 doses by age 17 with 53 injections and 3 oral doses of rotavirus.
The number of vaccines included in the current childhood vaccine schedule has quadrupled over the past 60 years, with several demanding multiple injections and boosters. During this exponential rise of CDC “recommended” schedules, the health of American children has plummeted.
Autoimmune diseases, learning disabilities, food allergies, chronic ailments, and childhood obesity have all risen. The overall health of this nation ranks very low compared to all other industrialized nations, dead last in most areas.
Vaccine false dogma is so heavy hardly anyone with authority, even in mainstream media, makes the connection between poor health with high vaccination rates. Instead, more, three added for 2016, are getting enforced by mandate or coerced by pediatricians who have the right to refuse medical care on kids who aren’t vaccinated.
Destroying Health with Vaccines is Good Business
50 Studies the AAP Avoided to Mention
There is a robust, worldwide body of published science from highly esteemed scientists questioning the safety of many different aspects of vaccines-how come we never hear from them? The majority of the most compelling science has been published since 2010. Below find 50 such studies to consider, sorted chronologically, and note that these studies only represent a portion of the published work implicating vaccinations in a wide variety of negative health outcomes.
The American Academy of Pediatrics made representations to President Trump in a letter dated 2/7/2017 that are utterly indefensible and inaccurate, as any rational review of the studies below quickly demonstrates. For example, the AAP wrote:
“Claims that vaccines are unsafe when administered according to expert recommendations have been disproven by a robust body of medical literature…we write to express our unequivocal support for the safety of vaccines.”
We contend that the AAP’s statements to the President are baseless, reckless, and easily refuted. The AAP’s letter alone supports the President’s desire to field a Vaccine Safety Commission and do all we can to make vaccines as safe as possible. Please click here for a list of all 50 studies detailed below.
New Guidelines for Safe Usage of Colloidal Silver
The Silver Safety Committee has announced its creation of the Silver Safety Pyramid, which is designed to enable anyone to easily determine safe usage levels of any dietary supplement containing silver, typically referred to as ionic silver or colloidal silver.
The Silver Safety Committee consists of doctors, chemistry professors and world leaders in health-freedom advocacy.
According to Herbert Slavin, M.D., director of the Institute of Advanced Medicine in Lauderhill, Florida, and a member of the Committee:
“This is an area where confusion and concern developed needlessly. Few things in life are as cut-and-dried as the fact that silver is completely safe when used within normal limits. The U.S. government provides a very clear guideline for the safe oral intake of silver. We’ve simply provided an easy method for applying that guideline to the safe use of any silver supplement product.”
The U.S. Environmental Protection Agency has a guideline called the Reference Dose (RfD) for safe limits on daily intake of silver. The EPA’s RfD guideline is specifically intended to keep a person’s intake of silver below the level that could possibly discolor the skin.
Says Jeffrey Blumer, M.D., Ph.D., director of the Center for Drug Research, the world’s largest clinical research center for pediatric drugs, and former director of the Greater Cleveland Poison Control Center:
“Common substances like table salt and aspirin are harmless with normal use, but excessive intake can become toxic and even life-threatening. With normal responsible usage, silver supplements are entirely harmless to humans.”
The Silver Safety Pyramid is based on the Committee’s Silver Safety Guideline, which recommends that a person’s intake of silver from dietary supplements be limited to 25 percent of the EPA’s recommended limit for total daily intake of silver.
It utilizes the Silver Safety Calculation, a simple mathematical formula that enables a person to easily determine how much to take of any silver-containing product to remain within the safety guidelines.
J Forensic Leg Med. 2007 Feb;14(2):87-91.
Abstract
The simultaneous sudden deaths of twins rarely occur and therefore it has received limited attention in the medical literature. When the deaths of the twins meet the defined criteria for sudden infant death syndrome (SIDS) independently and take place within the same 24 h range it can be called as simultaneous SIDS (SSIDS). The case(s): Twin girls (3.5-month-old) were found dead by their mother in their crib, both in supine position. The infants were identical twins and delivered at a hospital by cesarean section. Both infants were healthy and did not have any serious medical history. Two days prior to the incident, the twins had received the second dose of oral polio, DPT and the first dose of hepatitis B vaccines and they had fever on the first day of the vaccination and been given teaspoonful of acetaminophen. Death scene investigation, judicial investigation, parental assessment, macroscopic and microscopic autopsy findings and the toxicological analysis did not yield any specific cause of death. The case(s) were referred to a supreme board composed of multidisciplinary medical professionals at the Institute of Forensic Medicine, Ministry of Justice, in Istanbul. The Board decided that the available data was consistent with SIDS. These SIDS case(s) are presented because twin SIDS are rare and this is the first time that a simultaneous twin SIDS have been reported in Turkey. Simultaneous SIDS cases have many implications regarding definition, diagnosis and medico-legal approach.
J Toxicol Environ Health A. 2011;74(14):903-16. doi: 10.1080/15287394.2011.573736.
Abstract
The reason for the rapid rise of autism in the United States that began in the 1990s is a mystery. Although individuals probably have a genetic predisposition to develop autism, researchers suspect that one or more environmental triggers are also needed. One of those triggers might be the battery of vaccinations that young children receive. Using regression analysis and controlling for family income and ethnicity, the relationship between the proportion of children who received the recommended vaccines by age 2 years and the prevalence of autism (AUT) or speech or language impairment (SLI) in each U.S. state from 2001 and 2007 was determined. A positive and statistically significant relationship was found: The higher the proportion of children receiving recommended vaccinations, the higher was the prevalence of AUT or SLI. A 1% increase in vaccination was associated with an additional 680 children having AUT or SLI. Neither parental behavior nor access to care affected the results, since vaccination proportions were not significantly related (statistically) to any other disability or to the number of pediatricians in a U.S. state. The results suggest that although mercury has been removed from many vaccines, other culprits may link vaccines to autism. Further study into the relationship between vaccines and autism is warranted.
Ever wonder WHY we NEED a religious exemption from vaccines?
Are you aware that some vaccines are made from ABORTIONS?
Marcella Piper-Terry explains in detail how abortions are used in vaccine manufacturing and the implications of that.
Interview by Polly Tommey and camera by Joshua Coleman and Anu Vaidya with editing by Joshua Coleman.
The Vaxxed bus makes a special stop in Fort Wayne, Indiana to talk to Independent Researcher Marcella Piper-Terry about religious exemptions from vaccines and aborted fetal cells. Interview by Polly Tommey and camera by Joshua Coleman and Anu Vaidya with editing by Joshua Coleman.
Autism-Vaccine Theory Yet to Be Debunked
Contrary to the popular misconception, the autism-vaccine link has never been disproven. The autism-vaccine debate has been going around for decades, yet until recently, no official safety study has been done by the CDC itself. Many other studies done had either conflict of interest or insufficient data (most importantly, the CDC admits that a study comparing vaccinated versus unvaccinated children has never been done).
In 2004 when the CDC finally concluded a long-term study on vaccinations and autism in children, the results were not what they expected. They found a potential link between the two, primarily in African American boys, and decided to hide the information from the public.
Their study was published, but the significant information was not, instead it was literally thrown into a huge garbage can.
This came to light in 2014 when a senior scientist at the CDC, Dr. William Thompson came forward, admitting to what they did. Florida U.S. Representative Bill Posey spoke about it to the House of Representatives urging for an official investigation, but not much has been done since.
Healthy Children Can Become Horribly Sick After Vaccinations
For many, these stories are nothing but anecdotes, but for thousands of families who have gone through this (and doctors who witnessed it), it is a real tragedy. More people are coming forward with eerily similar stories. Seemingly healthy children become sick after receiving vaccinations (some within hours), and many never recover.
Public health officials and the CDC say that vaccines are necessary for public health, pointing to their effect on disease outbreaks such as polio, measles and other preventable diseases. But critics say they’re unwilling to fairly study or even discuss the other side of the question: vaccine injured people.
One of the reasons we might not hear about them is that the only place the affected families can go to report injuries is to VAERS, Vaccine Adverse Event Reporting System, created by the CDC and FDA.
The site welcomes its visitors with: “Have you or your child had a reaction following vaccination?”
After that, families can ask for monetary compensation from what many call the vaccine court, an administrative procedure, which is run by a government program called 1986 National Childhood Vaccine Injury Act using government-funded science. The act was passed in large part because of lobbying from pharmaceutical companies, which now cannot be sued for anything related to the vaccines they make — a clear conflict of interest.
Most importantly, these hearings are not open to the public or press, so we rarely hear about them.
Porter Bridges developed brain damage after childhood vaccinations. Photo: Bought movie.
Some stories do find a way to get noticed. In 1994 the Bridges family filed a suit through the National Vaccine Injury Compensation Program, after their son Porter became autistic. In 2011 they won the case and received about $7 million. The court concluded that a combination of childhood vaccines caused Porter to have encephalopathy – brain damage.
(Porter’s story was thoroughly discussed in the movie Bought, a film bringing light to the money involved in the pharmaceutical industry and its effect in making vaccines).
Injuries such as encephalopathy are controversial because the defendants may say the child does not have autism, they have encephalopathy, and the link between autism and vaccines is therefore “disproved.”
But autism spectrum conditions have grown to include many symptoms, and the main one is brain developmental issues. Whether in the future, studies will be able to classify encephalopathy or brain damage and autism as the same thing, it’s worth noting that the two have many identical symptoms: confusion, memory issues, muscle weakness, twitching, trembling, difficulty speaking, seizures, and even coma.
And encephalopathy is a common vaccine injury. The VAERS site lists it as a possible result of the DTP shot (noticeable within 72 hours) and MMR (within 5-15 days).
One of the most famous MMR court cases is that of Bailey Banks. The court concluded that childhood vaccinations caused Acute Disseminated Encephalomyelitis or ADEM (intense brain swelling).
The true numbers of injured are hard to count, as many families never report them or ask for compensation knowing that it might take up to two decades to see the results.
Vaccine Pamphlets Themselves List Many Serious Side-Effects
Every vaccine comes with a long insert of side-effects, which are rarely shown to patients. And if one were to ask, doctors have been known to get upset.
Looking at an insert from any vaccine paints a similar picture. This is an insert for M-M-R II vaccine (measles, mumps, and rubella) made by Merck, one of the first biggest pharmaceutical companies.
First of all, the safety of this particular vaccine has been determined by studies on a small number of children, 284 total.
The vaccine has also never been studied for its effect on the development of the fetus in pregnant women.
The safety of this vaccine, when given before the age of 12 months, has not been established. It is also not 100% effective, like all vaccines.
Patients who may experience an adverse reaction are instructed to report it to VAERS.
The list of the adverse reactions reported is long, but what is particularly important are injuries to the nervous system:
Encephalitis; encephalopathy; measles inclusion body encephalitis (MIBE); subacute sclerosing panencephalitis (SSPE); Guillain-Barré Syndrome (GBS); acute disseminated encephalomyelitis (ADEM); transverse myelitis; febrile convulsions; afebrile convulsions or seizures; ataxia; polyneuritis; polyneuropathy; ocular palsies; paresthesia.
In the 2016 VAERS report (not yet complete), encephalopathy is mentioned many times, as well as autism (mentioned 97 times).
Patients’ families reported: “loss of speech, regression from previous milestones, a light went out from child’s eyes, fever, lethargy, refusing to eat, encephalopathy.”
“Difficulty breathing, fever, hive-like rashes. Currently being assessed for Autism spectrum, speech loss, occupational therapy, etc.”
“Insomnia, anxiety, paranoia, (GABA) seizures, tics…legs would suddenly give out and she would fall, acne, headaches, stomach aches, dizziness, regression, anemia, mood swings, emotional lability, cognitive decline, brain inflammation.”
If only half of America is properly vaccinated, where are the epidemics?
The argument for herd immunity was actually developed out of observations of natural immunity, not vaccination. Statisticians observed that populations were protected when sufficient members contracted the wild form of a disease, and subsequently acquired lifelong immunity. With vaccines, however, evidence shows that unvaccinated children may catch infectious diseases from vaccinated children. What is true of natural immunity is not true of vaccination.
The herd immunity argument has always been inconsistent. On the one hand, the theory goes, people who cannot receive vaccines for whatever reason are protected from the disease through a high level of vaccination in the rest of society. On the other hand, the theory continues, parents who don’t vaccinate their children put the health of wider society at risk. How can a handful of people not getting vaccinated be protected from getting sick, while at the same time being so disease-ridden that they make others sick? This doesn’t make sense.
While herd immunity may not exist, herd mentality most definitely does. Health authorities, media commentators, and schools and their parent–teacher associations waste no opportunity in perpetuating this myth. Proponents have done such a thorough job of convincing the public that a parent who questions it is treated like someone who thinks the earth is flat or believes climate change is a conspiracy. On the contrary: an unprejudiced view of the science about vaccines, and an examination of history, clearly show that the herd immunity theory is—and always has been—flawed.
Vaccines may have a place in our medical arsenal, but they are not the silver bullet they’re portrayed to be. Year after year the pharmaceutical industry, looking for lucrative new profit centers, churns out new vaccines. They use pseudo-science to convince the public that these products are safe and effective, and they use public shaming to convince the citizenry that non-compliance is a public health threat. This entire racket completely falls apart with a close examination of the herd immunity myth. Until we are honest in our assessment of both the safety and efficacy of vaccines, kids will continue to be hurt, rights will continue to be trampled, and mythology will continue to trump science.
Gretchen DuBeau is Executive Director of Alliance for Natural Health USA.
The Vaccine Did It: Mutated MMR Mumps Virus in the Brain of a Child Caused His Death, British Researchers Confirm
Posted on:
Sunday, January 22nd 2017 at 6:30 pm
Written By:
Celeste McGovern
The Vaccine Did It
A toddler who developed severe neurological symptoms including blindness associated with chronic encephalitis and died following MMR vaccination was found to have vaccine-derived mumps virus in his brain, a new study reports.
Published in the current issue of the journal, Acta Neuropathologica, the study is the first of its kind to conclusively demonstrate chronic brain damage in the form of “panencephalitis” due to a vaccine-derived strain of the mumps virus. In light of a recent epidemic of mumps in highly vaccinated populations, the research raises questions about the dangers of live vaccine virus mutations and about public health claims that the MMR is a completely safe and effective vaccine without serious side effects. MMR, BRAIN INFECTION AND DEATH
The study describes an 18-month old infant who was diagnosed with Severe Combined Immunodeficiency Disease (SCID) — a serious immune system defect that may follow infection — four months after he received the triple Measles Mumps Rubella vaccine that contains live viruses.
The baby was treated for the illness but six months later became ill again with fever, rash, diarrhoea, lethargy and seizures. MRI scans of his brain showed evidence of encephalitis — brain inflammation due to infection.
The toddler was treated with antimicrobials, antivirals and steroids and sent home on anticonvulsant drugs. Over the next few months, behavioural problems became obvious, his hearing was impaired and his speech and language were delayed. A year later, by then four years old, he was still suffering from seizures and he became increasingly lethargic, disoriented and agitated. His walking was increasingly uncoordinated and he began to lose his eyesight.
A repeat MRI scan of the boy’s brain revealed abnormalities and a brain biopsy was taken at Great Ormond Street Hospital for Children in London. It revealed neuronal death and evidence of central nervous system damage and chronic inflammation. Despite aggressive treatment, his seizures increased, he became weak on his left side, went blind and the five-year-old died seven weeks later. VACCINE VIRUS CONFIRMED
Spinal fluid and urine samples collected during the boy’s last hospitalisation, as well as RNA re-extracted from his brain biopsy, were sent to the Public Health England Virus Reference Laboratory for sequencing.
Researchers, led by Sofia Morfopoulou of the Division of Infection and Immunity, University College London, and at the National Institute for Biological Standards and Control, used deep sequencing technology to identify the MuV -JL5 vaccine virus strain in the boy’s brain biopsy which was negative for all other viruses.
Genetic Drift and Outbreaks
Mutations in the mumps vaccine virus from that in the batch of the vaccine the boy had received were also detected. The study refers to a 2015 study confirming “genetic instability” of mumps vaccine virus that leads to “genetic drift” between different vaccine batches and may explain why some mumps vaccines induce more serious adverse reactions than others, especially when they are grown on different media.
This science may also explain why the mumps vaccine is failing. A recent outbreak among more than 1,600 mostly vaccinated people in Arkansas has public health officers there admitting that the vaccine isn’t protecting against emerging new strains of the virus.
It’s part of a growing phenomenon that scientists are reporting in many vaccines called “sero-conversion” – when vaccines diminish the strain of a virus they are targeting, but another strain of the same virus blooms — just as antibiotics wipe out bacterial infections but leave antibiotic-resistant superbugs to thrive.
Study : The administration of intranasal live attenuated influenza vaccine induces changes in the nasal microbiota and nasal epithelium gene expression profiles Background
Viral infections such as influenza have been shown to predispose hosts to increased colonization of the respiratory tract by pathogenic bacteria and secondary bacterial pneumonia. To examine how viral infections and host antiviral immune responses alter the upper respiratory microbiota, we analyzed nasal bacterial composition by 16S ribosomal RNA (rRNA) gene sequencing in healthy adults at baseline and at 1 to 2 weeks and 4 to 6 weeks following instillation of live attenuated influenza vaccine or intranasal sterile saline. A subset of these samples was submitted for microarray host gene expression profiling. Results
We found that live attenuated influenza vaccination led to significant changes in microbial community structure, diversity, and core taxonomic membership as well as increases in the relative abundances of Staphylococcus and Bacteroides genera (both p < 0.05). Hypergeometric testing for the enrichment of gene ontology terms in the vaccinated group reflected a robust up-regulation of type I and type II interferon-stimulated genes in the vaccinated group relative to controls. Translational murine studies showed that poly I:C administration did in fact permit greater nasal Staphylococcus aureus persistence, a response absent in interferon alpha/beta receptor deficient mice. Conclusions
Collectively, our findings demonstrate that although the human nasal bacterial community is heterogeneous and typically individually robust, activation of a type I interferon (IFN)-mediated antiviral response may foster the disproportionate emergence of potentially pathogenic species such as S. aureus.
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