Vaccine Injury: Brain Damage
Merck acknowledges that vaccines cause brain damage and auto immune diseases
"Encephalitis is inflammation of the brain that occurs when a virus directly infects the brain or when a virus, vaccine, or something else triggers inflammation. The spinal cord may also be involved, resulting in a disorder called encephalomyelitis."
"Encephalitis can occur when a virus or vaccine triggers a reaction that makes the immune system attack brain tissue (an autoimmune reaction)."
So says the Merck Manual, a common reference book for medical professionals published by one of the largest pharmaceutical companies on the planet.
Click here to visit the Merck Manual page on encephalitis.
"Encephalitis can occur when a virus or vaccine triggers a reaction that makes the immune system attack brain tissue (an autoimmune reaction)."
So says the Merck Manual, a common reference book for medical professionals published by one of the largest pharmaceutical companies on the planet.
Click here to visit the Merck Manual page on encephalitis.
CDC Identifies 760% Increase in Autism Diagnoses in Vaccinated Children
In 1999 the CDC found a 760% increase in diagnoses of autism in children who received 25 micrograms of mercury via vaccination in their first month of live compared to those who received none in that time period. Considering this is in all likelihood from just one vaccine, not the entire schedule of vaccines recommended for school entry, this is huge increase that points to the possibility of an even more massive one.
Click here to read the report of their initial findings.
Click here to read the report of their initial findings.
Head of Vaccine Safety for the U.K. Links MMR and Autism
Dr. Peter Fletcher, former Chief Scientific Officer at the Department of Health in the UK:
"I have always thought since I first heard about the Somali children that this really proves the causal role of vaccines. The Amish children who have no vaccines have no autistic-like disorders and the Somali children who are newly exposed to aggressive vaccine programmes have exceptionally high levels! What more evidence is needed?”
Click here to read the entire article with many excerpts of Dr. Fletcher's words from an interview on the subject. It was published in March, 2016 in the "Daily Mail."
"I have always thought since I first heard about the Somali children that this really proves the causal role of vaccines. The Amish children who have no vaccines have no autistic-like disorders and the Somali children who are newly exposed to aggressive vaccine programmes have exceptionally high levels! What more evidence is needed?”
Click here to read the entire article with many excerpts of Dr. Fletcher's words from an interview on the subject. It was published in March, 2016 in the "Daily Mail."
Autism Tied To Increasing Vaccines Finds City University of New York
"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."
Click here to read the abstract of the study published in 2011 in the "Journal of Toxicology and Environmental Health."
Click here to read the abstract of the study published in 2011 in the "Journal of Toxicology and Environmental Health."
Maternal Infection Increases Risk of Autism Diagnosis
"These findings indicate that maternal infection during pregnancy increases the risk of ASD in offspring. Possible mechanisms may include direct effects of pathogens and, more indirectly, the effects of inflammatory responses on the developing brain."
Click here to read the abstract of the study published in June, 2016 by a team of Chinese researchers.
Click here to read the abstract of the study published in June, 2016 by a team of Chinese researchers.
Comprehensive Literature Review Finds Autism Linked to Vaccines
"Searching information from 1943 to the present in PubMed and Ovid Medline databases, this review summarizes results that correlate the timing of changes in incidence with environmental changes. Autism could result from more than one cause, with different manifestations in different individuals that share common symptoms. Documented causes of autism include genetic mutations and/or deletions, viral infections, and encephalitis following vaccination. Therefore, autism is the result of genetic defects and/or inflammation of the brain. The inflammation could be caused by a defective placenta, immature blood-brain barrier, the immune response of the mother to infection while pregnant, a premature birth, encephalitis in the child after birth, or a toxic environment."
Click here to read the abstract of the study published in January, 2011 in the "Journal of Immunotoxicology."
Click here to read the abstract of the study published in January, 2011 in the "Journal of Immunotoxicology."
Government Data and Science Link Mercury in Vaccines to Autism
"Exposure to mercury can cause immune, sensory, neurological, motor, and behavioral dysfunctions similar to traits defining or associated with autism, and the similarities extend to neuroanatomy, neurotransmitters, and biochemistry.
Thimerosal, a preservative added to many vaccines, has become a major source of mercury in children who, within their first two years, may have received a quantity of mercury that exceeds safety guidelines.
A review of medical literature and US government data suggests that: (i) many cases of idiopathic autism are induced by early mercury exposure from thimerosal; (ii) this type of autism represents an unrecognized mercurial syndrome; and (iii) genetic and non-genetic factors establish a predisposition whereby thimerosal's adverse effects occur only in some children."
Click here to read the abstract of the review published in April, 2001 in the journal, "Medical Hypotheses."
Thimerosal, a preservative added to many vaccines, has become a major source of mercury in children who, within their first two years, may have received a quantity of mercury that exceeds safety guidelines.
A review of medical literature and US government data suggests that: (i) many cases of idiopathic autism are induced by early mercury exposure from thimerosal; (ii) this type of autism represents an unrecognized mercurial syndrome; and (iii) genetic and non-genetic factors establish a predisposition whereby thimerosal's adverse effects occur only in some children."
Click here to read the abstract of the review published in April, 2001 in the journal, "Medical Hypotheses."
Leading Aluminum Neurotoxicologist Finds Vaccines Causative Factor in Autism
"Autism spectrum disorders (ASD) are serious multisystem developmental disorders and an urgent global public health concern. Dysfunctional immunity and impaired brain function are core deficits in ASD. Aluminum (Al), the most commonly used vaccine adjuvant, is a demonstrated neurotoxin and a strong immune stimulator. Hence, adjuvant Al has the potential to induce neuroimmune disorders."
"Our results show that: (i) children from countries with the highest ASD prevalence appear to have the highest exposure to Al from vaccines; (ii) the increase in exposure to Al adjuvants significantly correlates with the increase in ASD prevalence in the United States observed over the last two decades (Pearson r=0.92, p<0.0001); and (iii) a significant correlation exists between the amounts of Al administered to preschool children and the current prevalence of ASD in seven Western countries, particularly at 3-4 months of age (Pearson r=0.89-0.94, p=0.0018-0.0248)."
Click here to read their findings, published in November, 2011 in the "Journal of Inorganic Biochemistry."
"Our results show that: (i) children from countries with the highest ASD prevalence appear to have the highest exposure to Al from vaccines; (ii) the increase in exposure to Al adjuvants significantly correlates with the increase in ASD prevalence in the United States observed over the last two decades (Pearson r=0.92, p<0.0001); and (iii) a significant correlation exists between the amounts of Al administered to preschool children and the current prevalence of ASD in seven Western countries, particularly at 3-4 months of age (Pearson r=0.89-0.94, p=0.0018-0.0248)."
Click here to read their findings, published in November, 2011 in the "Journal of Inorganic Biochemistry."
Prenatal Mercury Exposure May be Linked to Autism
"Children with ASDs were significantly more likely (odds ratio 2.35) to have Rh-negative mothers than controls. Each ASD patient's mother was determined to have been administered a TCR during her pregnancy.
The results provide insights into the potential role prenatal mercury exposure may play in some children with ASDs."
Click here to read the abstract of the study published in May, 2007 in "The Journal of Maternal-Fetal and Neonatal Medicine."
The results provide insights into the potential role prenatal mercury exposure may play in some children with ASDs."
Click here to read the abstract of the study published in May, 2007 in "The Journal of Maternal-Fetal and Neonatal Medicine."
Review of 266 Studies Finds Vaccines Lead to Autism
The mass of scientific evidence compiled by researchers clearly indicates that the incidence of autism occurs following vaccination and is most closely associated with the schedule of vaccines culminating in the MMR vaccine. That vaccines suppress natural immune function is not in dispute e.g. those with naturally low levels of immune function (immigrants from tropical climates) show greater predisposition to autistic spectrum disorders.
Click here to read the entire study, published in July, 2009 in the "North American Journal of Medical Sciences.
Click here to read the entire study, published in July, 2009 in the "North American Journal of Medical Sciences.
Vaccine Salesman and Chemistry Professor Debate Vaccine Autism Link
This is a debate between two doctors.
On the one hand is a guy who patented a vaccine. He now holds a position at a university selling vaccines. His salary is paid by vaccine manufacturers. He states that vaccines are safe and effective and have no relationship to autism. He does not provide any evidence or science.
The other guy is the retired chair of the chemistry department at the University of Kentucky and a world leader in the study of mercury toxicology. He states that vaccines have been given credit they do not deserve, they are dangerous and they are related to autism. He uses government data and hard science.
Click here to watch this debate on youtube.
On the one hand is a guy who patented a vaccine. He now holds a position at a university selling vaccines. His salary is paid by vaccine manufacturers. He states that vaccines are safe and effective and have no relationship to autism. He does not provide any evidence or science.
The other guy is the retired chair of the chemistry department at the University of Kentucky and a world leader in the study of mercury toxicology. He states that vaccines have been given credit they do not deserve, they are dangerous and they are related to autism. He uses government data and hard science.
Click here to watch this debate on youtube.
University of Texas Associates Autism with Mercury in Vaccines
"The present study provides new epidemiological evidence supporting an association between increasing organic-Hg exposure from Thimerosal-containing childhood vaccines and the subsequent risk of an ASD diagnosis."
Click here to read their entire study published in December, 2013 in the journal, "Translational Neurodegeneration."
Click here to read their entire study published in December, 2013 in the journal, "Translational Neurodegeneration."
University of Northern Iowa Finds Autism Related to Metal Toxicity
"The various causes that have led to the increase in autism diagnosis are likely multi-faceted, and understanding the causes is one of the most important health topics today. We argue that scientific research does not support rejecting the link between the neurodevelopmental disorder of autism and toxic exposures."
Click here to read the study from 2010.
Click here to read the study from 2010.
Autism Caused by Metal Toxicity, Successfully Treated by Chelation
"Lead and mercury considered as one of the main causes of autism. Environmental exposure as well as defect in heavy metal metabolism is responsible for the high level of heavy metals. Detoxification by chelating agents had great role in improvement of those kids."
Click here to read an abstract of the findings by researchers in Egypt in the Forensic Medicine and Clinical Toxicology Department of the Faculty of Medicine at Assiut University. They published their findings in November, 2014 in the journal, "Environmental Toxicology and Pharmacology."
Click here to read an abstract of the findings by researchers in Egypt in the Forensic Medicine and Clinical Toxicology Department of the Faculty of Medicine at Assiut University. They published their findings in November, 2014 in the journal, "Environmental Toxicology and Pharmacology."
A Case Review Finds Autism Due to Vaccines and Their Ingredients
"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."
Click here to read the abstract of the study published in May, 2007 in the "Journal of Toxicological and Environmental Health."
Click here to read the abstract of the study published in May, 2007 in the "Journal of Toxicological and Environmental Health."
Autism Linked to Metal Toxicity and Nutritional Deficiency
"By comparing hair concentration of autistic vs nonautistic children, elevated hair concentrations were noted for aluminum, arsenic, cadmium, mercury, antimony, nickel, lead, and vanadium. Hair levels of calcium, iron, iodine, magnesium, manganese, molybdenum, zinc, and selenium were considered deficient.
There was a significant positive correlation between lead & verbal communication. In addition, there was a significant negative correlation between zinc & fear and nervousness.
Our data supports the historic evidence that heavy metals play a role in the development of ASD. In combination with an inadequate nutritional status the toxic effect of metals increase along with the severity of symptoms."
Click here to read the findings of a team of researchers from around the world. They published their results in January, 2012 in the journal, "Maedica."
The interactions between genes and the environment are now regarded as the most probable explanation for autism. In this review, we summarize the results of a metallomics study in which scalp hair concentrations of 26 trace elements were examined for 1,967 autistic children (1,553 males and 414 females aged 0–15 years-old), and discuss recent advances in our understanding of epigenetic roles of infantile mineral imbalances in the pathogenesis of autism.
In the 1,967 subjects, 584 (29.7%) and 347 (17.6%) were found deficient in zinc and magnesium, respectively, and the incidence rate of zinc deficiency was estimated at 43.5% in male and 52.5% in female infantile subjects aged 0–3 years-old.
In contrast, 339 (17.2%), 168 (8.5%) and 94 (4.8%) individuals were found to suffer from high burdens of aluminum, cadmium and lead, respectively, and 2.8% or less from mercury and arsenic. High toxic metal burdens were more frequently observed in the infants aged 0–3 years-old, whose incidence rates were 20.6%, 12.1%, 7.5%, 3.2% and 2.3% for aluminum, cadmium, lead, arsenic and mercury, respectively.
These findings suggest that infantile zinc and magnesium-deficiency and/or toxic metal burdens may be critical and induce epigenetic alterations in the genes and genetic regulation mechanisms of neurodevelopment in the autistic children, and demonstrate that a time factor “infantile window” is also critical for neurodevelopment and probably for therapy. Thus, early metallomics analysis may lead to early screening/estimation and treatment/prevention for the autistic neurodevelopment disorders.
Click here to read the findings of a group of Japanese researchers published in November, 2013 in the "International Journal of Environmental Research and Public Health."
There was a significant positive correlation between lead & verbal communication. In addition, there was a significant negative correlation between zinc & fear and nervousness.
Our data supports the historic evidence that heavy metals play a role in the development of ASD. In combination with an inadequate nutritional status the toxic effect of metals increase along with the severity of symptoms."
Click here to read the findings of a team of researchers from around the world. They published their results in January, 2012 in the journal, "Maedica."
The interactions between genes and the environment are now regarded as the most probable explanation for autism. In this review, we summarize the results of a metallomics study in which scalp hair concentrations of 26 trace elements were examined for 1,967 autistic children (1,553 males and 414 females aged 0–15 years-old), and discuss recent advances in our understanding of epigenetic roles of infantile mineral imbalances in the pathogenesis of autism.
In the 1,967 subjects, 584 (29.7%) and 347 (17.6%) were found deficient in zinc and magnesium, respectively, and the incidence rate of zinc deficiency was estimated at 43.5% in male and 52.5% in female infantile subjects aged 0–3 years-old.
In contrast, 339 (17.2%), 168 (8.5%) and 94 (4.8%) individuals were found to suffer from high burdens of aluminum, cadmium and lead, respectively, and 2.8% or less from mercury and arsenic. High toxic metal burdens were more frequently observed in the infants aged 0–3 years-old, whose incidence rates were 20.6%, 12.1%, 7.5%, 3.2% and 2.3% for aluminum, cadmium, lead, arsenic and mercury, respectively.
These findings suggest that infantile zinc and magnesium-deficiency and/or toxic metal burdens may be critical and induce epigenetic alterations in the genes and genetic regulation mechanisms of neurodevelopment in the autistic children, and demonstrate that a time factor “infantile window” is also critical for neurodevelopment and probably for therapy. Thus, early metallomics analysis may lead to early screening/estimation and treatment/prevention for the autistic neurodevelopment disorders.
Click here to read the findings of a group of Japanese researchers published in November, 2013 in the "International Journal of Environmental Research and Public Health."
Developmental Disorders Due to Industrial Toxins, Including Mercury
"Neurodevelopmental disabilities, including autism, attention-deficit hyperactivity disorder, dyslexia, and other cognitive impairments, affect millions of children worldwide, and some diagnoses seem to be increasing in frequency. Industrial chemicals that injure the developing brain are among the known causes for this rise in prevalence."
They mention methylmercury but not ethylmercury. Mercury is as toxic in the ethyl state as the methyl state, if not more so. Many scientists who have challenged vaccines have lost their funding. But if you are smart enough to read between the lines, you'll get it.
Click here to read this study published in "The Lancet" in 2014.
They mention methylmercury but not ethylmercury. Mercury is as toxic in the ethyl state as the methyl state, if not more so. Many scientists who have challenged vaccines have lost their funding. But if you are smart enough to read between the lines, you'll get it.
Click here to read this study published in "The Lancet" in 2014.
MMR and Brain Antibodies Found in Autistic Children
MMR antibodies found in 60% of autistic kids, 0% of non autistic kids.
90% of them also had antibodies to their own brains.
Click here to read the abstract of the lab findings of researchers in the Department of Biology and Biotechnology Center at Utah State University published the in 2002 in the "Journal of Biomedical Science."
"The level of measles antibody was significantly higher in autistic children as compared with normal children or siblings of autistic children.
The antibody to this antigen was found in 83% of autistic children but not in normal children or siblings of autistic children.
Thus autistic children have a hyper immune response to measles virus, which in the absence of a wild type of measles infection might be a sign of an abnormal immune reaction to the vaccine strain or virus reactivation."
Click here to read an earlier study by the same researchers examining the relationship between virus and brain antibodies published in 1998 in the journal "Clinical Immunology and Immunopathology."
"Many autistic children harbored brain myelin basic protein autoantibodies and elevated levels of antibodies to measles virus and measles-mumps-rubella (MMR) vaccine.
Measles might be etiologically linked to autism because measles and MMR antibodies (a viral marker) correlated positively to brain autoantibodies (an autoimmune marker)--salient features that characterize autoimmune pathology in autism."
Click here to read the abstract of the study published in 2009 in the journal, "Annals of Clinical Psychiatry."
90% of them also had antibodies to their own brains.
Click here to read the abstract of the lab findings of researchers in the Department of Biology and Biotechnology Center at Utah State University published the in 2002 in the "Journal of Biomedical Science."
"The level of measles antibody was significantly higher in autistic children as compared with normal children or siblings of autistic children.
The antibody to this antigen was found in 83% of autistic children but not in normal children or siblings of autistic children.
Thus autistic children have a hyper immune response to measles virus, which in the absence of a wild type of measles infection might be a sign of an abnormal immune reaction to the vaccine strain or virus reactivation."
Click here to read an earlier study by the same researchers examining the relationship between virus and brain antibodies published in 1998 in the journal "Clinical Immunology and Immunopathology."
"Many autistic children harbored brain myelin basic protein autoantibodies and elevated levels of antibodies to measles virus and measles-mumps-rubella (MMR) vaccine.
Measles might be etiologically linked to autism because measles and MMR antibodies (a viral marker) correlated positively to brain autoantibodies (an autoimmune marker)--salient features that characterize autoimmune pathology in autism."
Click here to read the abstract of the study published in 2009 in the journal, "Annals of Clinical Psychiatry."
Brain Damage Linked to Aluminum and GMOs by MIT
"Many neurological diseases, including autism, depression, dementia, anxiety disorder and Parkinson’s disease, are associated with abnormal sleep patterns, which are directly linked to pineal gland dysfunction. The pineal gland is highly susceptible to environmental toxicants. Two pervasive substances in modern industrialized nations are aluminum and glyphosate, the active ingredient in the herbicide, Roundup?. In this paper, we show how these two toxicants work synergistically to induce neurological damage.
Premature birth is associated with hypoxic stress and with substantial increased risk to the subsequent development of autism, linking hypoxia to autism.
This leads to anemia-induced hypoxia, promoting neurotoxicity and damaging the pineal gland.
Both glyphosate and aluminum disrupt cytochrome P450 enzymes, which are involved in melatonin metabolism. Furthermore, melatonin is derived from tryptophan, whose synthesis in plants and microbes is blocked by glyphosate.
We also demonstrate a plausible role for vitamin D3 dysbiosis in impaired gut function and impaired serotonin synthesis."
Click here to read the entire paper by a team at MIT, published in January, 2015 by "Scientific Research."
Premature birth is associated with hypoxic stress and with substantial increased risk to the subsequent development of autism, linking hypoxia to autism.
This leads to anemia-induced hypoxia, promoting neurotoxicity and damaging the pineal gland.
Both glyphosate and aluminum disrupt cytochrome P450 enzymes, which are involved in melatonin metabolism. Furthermore, melatonin is derived from tryptophan, whose synthesis in plants and microbes is blocked by glyphosate.
We also demonstrate a plausible role for vitamin D3 dysbiosis in impaired gut function and impaired serotonin synthesis."
Click here to read the entire paper by a team at MIT, published in January, 2015 by "Scientific Research."
Structural and functional features of cns lymphatic vessels
"Autism spectrum disorders (ASD) represent an apparent pandemic threat to child development with the current CDC data documenting ASD affecting over 2% of U.S. males of school age ([CDC] Developmental Disabilities Monitoring Network Surveillance Year 2010 Principal, 2014).
ASD are likely a heterogeneous group of disorders with genetic and environmental causes resulting in similar phenotypes. Genetic contributions to autism are extremely heterogeneous and may involve synaptic formation and maturation."
Click here to read an analysis published in December, 2015 in the journal, "Frontiers in Neuroscience."
"One of the characteristics of the CNS is the lack of a classical lymphatic drainage system. Although it is now accepted that the CNS undergoes constant immune surveillance that takes place within the meningeal compartment, the mechanisms governing the entrance and exit of immune cells from the CNS remain poorly understood. In searching for T cell gateways into and out of the meninges, we discovered functional lymphatic vessels lining the dural sinuses. These structures express all of the molecular hallmarks of lymphatic endothelial cells, are able to carry both fluid and immune cells from the CSF, and are connected to the deep cervical lymph nodes. The unique location of these vessels may have impeded their discovery to date, thereby contributing to the long-held concept of the absence of lymphatic vasculature in the CNS. The discovery of the CNS lymphatic system may call for a reassessment of basic assumptions in neuroimmunology and shed new light on the etiology of neuroinflammatory and neurodegenerative diseases associated with immune system dysfunction."
Click here to read the study that found immune system structures in the brain. This discovery turns on its head over a century of conventional thought on the matter.
ASD are likely a heterogeneous group of disorders with genetic and environmental causes resulting in similar phenotypes. Genetic contributions to autism are extremely heterogeneous and may involve synaptic formation and maturation."
Click here to read an analysis published in December, 2015 in the journal, "Frontiers in Neuroscience."
"One of the characteristics of the CNS is the lack of a classical lymphatic drainage system. Although it is now accepted that the CNS undergoes constant immune surveillance that takes place within the meningeal compartment, the mechanisms governing the entrance and exit of immune cells from the CNS remain poorly understood. In searching for T cell gateways into and out of the meninges, we discovered functional lymphatic vessels lining the dural sinuses. These structures express all of the molecular hallmarks of lymphatic endothelial cells, are able to carry both fluid and immune cells from the CSF, and are connected to the deep cervical lymph nodes. The unique location of these vessels may have impeded their discovery to date, thereby contributing to the long-held concept of the absence of lymphatic vasculature in the CNS. The discovery of the CNS lymphatic system may call for a reassessment of basic assumptions in neuroimmunology and shed new light on the etiology of neuroinflammatory and neurodegenerative diseases associated with immune system dysfunction."
Click here to read the study that found immune system structures in the brain. This discovery turns on its head over a century of conventional thought on the matter.
Many Studies Suggest Possible Vaccine-Autism Links
"The disparaged scientists include well-published neurologists, pharmacists, epidemiologists, immunologists, PhD’s, chemists and microbiologists from places like Boston Children’s Hospital, Horizon Molecular Medicine at Georgia State University, University of British Columbia, City College of New York, Columbia University, Stony Brook University Medical Center, University of Northern Iowa, University of Michigan, University of Arkansas for Medical Sciences, Arkansas Children’s Hospital Research Institute, Al Azhar University of Cairo, Kinki University in Japan, the University of Pittsburgh School of Medicine, Swinburne University of Technology in Australia, Institute of Psychiatry and Neurology in Poland, Department of Child Health Care, Children’s Hospital of Fudan University in China, Utah State University and many more."
Click here to read this article on the attempt by the media to discredit scientists. It appears to be working. There are also many valuable links to scientific studies on the dangers of brain damage from vaccines.
Click here to read this article on the attempt by the media to discredit scientists. It appears to be working. There are also many valuable links to scientific studies on the dangers of brain damage from vaccines.
Association found between autism prevalence and childhood vaccination
"The higher the proportion of children receiving recommended vaccinations, the higher was the prevalence of autism or speech or language impairment."
This was the finding of a study published in 2011 in the "Journal of Toxicology and Environmental Health" by a researcher from the City University of New York.
Click here to read the abstract from the National Institutes of Health.
This was the finding of a study published in 2011 in the "Journal of Toxicology and Environmental Health" by a researcher from the City University of New York.
Click here to read the abstract from the National Institutes of Health.
Chair of Chemistry at the University of Kentucky Explains the Autism Epidemic
"It's farm boy logic. It was high school science.
I feel like I've been in a fifteen year argument with the town drunk" (referring to his attempts, as the chair of chemistry at the University of Kentucky and a leading expert on mercury toxicity, to try and speak with the CDC about the dangers of mercury.)
Dr. Boyd Haley recently retired as chair of chemistry at the University of Kentucky. His specialty was mercury toxicity. He has published a significant body of work and collaborated with top researchers around the world.
In this six minute video he breaks down the parameters of the autism epidemic, explaining in broad strokes what we know and where the questions are. He also fumes a little about his frustration trying to communicate with government "scientists" who seem unable to understand the basics of science.
Click here to watch the six minute video on youtube.
I feel like I've been in a fifteen year argument with the town drunk" (referring to his attempts, as the chair of chemistry at the University of Kentucky and a leading expert on mercury toxicity, to try and speak with the CDC about the dangers of mercury.)
Dr. Boyd Haley recently retired as chair of chemistry at the University of Kentucky. His specialty was mercury toxicity. He has published a significant body of work and collaborated with top researchers around the world.
In this six minute video he breaks down the parameters of the autism epidemic, explaining in broad strokes what we know and where the questions are. He also fumes a little about his frustration trying to communicate with government "scientists" who seem unable to understand the basics of science.
Click here to watch the six minute video on youtube.
Conjugate Vaccines Could be Related to Massive Rise in Autism
"It is hypothesized here that the introduction of the Hib conjugate vaccine in the US in 1988 and its subsequent introduction in Denmark and Israel could explain a substantial portion of the initial increases in ASDs in those countries. The continuation of the trend toward increased rates of ASDs could be further explained by increased usage of the vaccine, a change in 1990 in the recommended age of vaccination in the US from 15 to 2 months, increased immunogenicity of the vaccine through changes in its carrier protein, and the subsequent introduction of the conjugate vaccine for Streptococcus pneumoniae."
Click here to read the abstract of the paper published in December, 2011 in the journal, "Medical Hypotheses."
Click here to read the abstract of the paper published in December, 2011 in the journal, "Medical Hypotheses."
Cost of Treating Autism Expected to Approach One Trillion Dollars per Year
Autism is a complex condition with multiple causes but can be summed up as metal neurotoxicity compounded by genetic and immune disruptions. There are a number of ways that these disturbances can occur. The most ubiquitous and intimate is vaccination.
In ten years roughly five percent of our economy will be dedicated to caring for those so injured. And the percentage will grow.
Click here to read about the study from the University of California.
In ten years roughly five percent of our economy will be dedicated to caring for those so injured. And the percentage will grow.
Click here to read about the study from the University of California.
Polish Researchers Find Benefits of Vaccination May Not Outweigh Neurological Risk
"The present review summarizes data on neurological adverse events following vaccination in the relation to intensity, time of onset, taking into account the immunological and non-immunological mechanisms. The authors described the physio-logical development of the immune system and the possible immune system responses following vaccination. Toxic property of thimerosal, a mercury containing preservative used in some
vaccines was presented. The neurological complications after vaccination were described. The role of vaccination in the natural course of infectious diseases and the current immunizations schedule in Poland was discussed."
Click here to read this discussion by researchers in the Department of Pediatric Rehabilitation of the Medical University of Bialystok in Poland. It was published on the website of the university in 2012.
vaccines was presented. The neurological complications after vaccination were described. The role of vaccination in the natural course of infectious diseases and the current immunizations schedule in Poland was discussed."
Click here to read this discussion by researchers in the Department of Pediatric Rehabilitation of the Medical University of Bialystok in Poland. It was published on the website of the university in 2012.
1/45 Three to Nine Year Olds Diagnosed with Autism
The autism rate jumps again. This matches first hand reports that nursery school kids are more brain damaged each year. The number among two year olds is thought to be quite a bit higher, as the percentage seems to be rising each year.
They note in the article that autism diagnosis is often tied to flu during pregnancy.
A five fold increase in the flu has been noted among the vaccinated.
It is known that autism is related to mercury. Mercury in maternal blood accumulates in higher concentrations in fetal blood.
They also note that several studies have failed to link vaccines and autism. This is true. But thousands of studies have succeeded in establishing the link.
They claim the link with vaccines has been disproved. You can read the science here and decide for yourself if this is the case.
Click here to read the article from the NBC website from November, 2015.
They note in the article that autism diagnosis is often tied to flu during pregnancy.
A five fold increase in the flu has been noted among the vaccinated.
It is known that autism is related to mercury. Mercury in maternal blood accumulates in higher concentrations in fetal blood.
They also note that several studies have failed to link vaccines and autism. This is true. But thousands of studies have succeeded in establishing the link.
They claim the link with vaccines has been disproved. You can read the science here and decide for yourself if this is the case.
Click here to read the article from the NBC website from November, 2015.
Suicide Rate 900% of Average Among Autistic Adults, Life Spans 16 Years Shorter
The rate of autistic adults visiting emergency rooms more than doubled between 2006 and 2011. It jumped from 2.55% to 6.09% of total emergency room visits. 15% of those visits were for psychiatric complaints, nearly four times the rate for non autistic adults.
The suicide rate among high functioning autistic adults is nine times the national average and their life expectancy is sixteen years lower than the norm.
Click here to read the study by researchers at West Virginia University published in 2016.
The suicide rate among high functioning autistic adults is nine times the national average and their life expectancy is sixteen years lower than the norm.
Click here to read the study by researchers at West Virginia University published in 2016.
DNA Fragments In Vaccines Contribute to Autism
"Not only damaged human cells, but also healthy human cells can take up foreign DNA spontaneously. Foreign human DNA taken up by human cells will be transported in to nuclei and be integrated in to host genome, which will cause phenotype changes.
Hence, residual human fetal DNA fragments in vaccines can be one of the causes of autism spectrum disorder in children."
So found Dr. Theresa Deisher, Stanford trained molecular and cellular physiologist who was the first to find stem cells in adult hearts.
http://s3.amazonaws.com/soundchoice/soundchoice/wp-content/uploads/2012/08/DNA_Contaminants_in_Vaccines_Can_Integrate_Into_Childrens_Genes.pdf
Click here to read her findings.
Hence, residual human fetal DNA fragments in vaccines can be one of the causes of autism spectrum disorder in children."
So found Dr. Theresa Deisher, Stanford trained molecular and cellular physiologist who was the first to find stem cells in adult hearts.
http://s3.amazonaws.com/soundchoice/soundchoice/wp-content/uploads/2012/08/DNA_Contaminants_in_Vaccines_Can_Integrate_Into_Childrens_Genes.pdf
Click here to read her findings.
Autism: Metal Neurotoxicity
Autism is just a fancy word for brain damage. It is the symptoms of brain damage, specifically the symptoms of brain damage from metal poisoning. We have stopped using the word autism and started using the correct terms, brain damage and metal toxicity.
Brain damage has many well known causes. One prominent, common cause is environmental toxins, specifically industrial metals like mercury and aluminum. This is well documented, even on government websites such as the CDC and NIH.
The doses of these things given in vaccines to babies weighing just a few pounds are doses considered toxic to adults ranging from 350 to 1500 pounds, depending on how many vaccines are given at a time, etc.
Worse than that, these substances are known to accumulate in the brain and continue damaging it over time, so it is not just the original injury, but the ongoing damage that is a problem. Essentially, they are like little molecular knives running around the brain, forever.
It gets worse yet. Polysorbate 80 is added to many vaccines. It is a chemical that is added to drugs specifically to help them target the brain. The brain is covered by protective mechanisms called the blood brain barrier. The purpose of this barrier is to protect the brain from all but the purest things in the blood. Polysorbate 80 breaks down that barrier. It is added to drugs targeting the brain specifically because it helps them get through the barrier. It is added to vaccines where it helps the viruses, bacteria, mercury and aluminum get into the brain.
We won't write here about the synergistic damage of all these things when combined with fluoride and glyphosate, or round up. These synergistic effects have been thoroughly studied and well documented. We will post these studies asap.
Brain damage has many well known causes. One prominent, common cause is environmental toxins, specifically industrial metals like mercury and aluminum. This is well documented, even on government websites such as the CDC and NIH.
The doses of these things given in vaccines to babies weighing just a few pounds are doses considered toxic to adults ranging from 350 to 1500 pounds, depending on how many vaccines are given at a time, etc.
Worse than that, these substances are known to accumulate in the brain and continue damaging it over time, so it is not just the original injury, but the ongoing damage that is a problem. Essentially, they are like little molecular knives running around the brain, forever.
It gets worse yet. Polysorbate 80 is added to many vaccines. It is a chemical that is added to drugs specifically to help them target the brain. The brain is covered by protective mechanisms called the blood brain barrier. The purpose of this barrier is to protect the brain from all but the purest things in the blood. Polysorbate 80 breaks down that barrier. It is added to drugs targeting the brain specifically because it helps them get through the barrier. It is added to vaccines where it helps the viruses, bacteria, mercury and aluminum get into the brain.
We won't write here about the synergistic damage of all these things when combined with fluoride and glyphosate, or round up. These synergistic effects have been thoroughly studied and well documented. We will post these studies asap.
Review of the Literature Finds Mercury Causes Biological Deficits Leading to Autism
"Hg has been found to cause immune, sensory, neurological, motor, and behavioural dysfunctions similar to traits defining/associated with ASDs, and that these similarities extend to neuroanatomy, neurotransmitters, and biochemistry. Furthermore, a review of molecular mechanisms indicates that Hg exposure can induce death, disorganization and/or damage to selected neurons in the brain similar to that seen in recent ASD brain pathology studies, and this alteration may likely produce the symptoms by which ASDs are diagnosed. Finally, a review of treatments suggests that ASD patients who undergo protocols to reduce Hg and/or its effects show significant clinical improvements in some cases. In conclusion, the overwhelming preponderance of the evidence favours acceptance that Hg exposure is capable of causing some ASDs."
Click here to read the abstract of the review published in October, 2008 in the "Indian Journal of Medical Research."
"Several recent studies suggest that children diagnosed with an ASD have abnormal sulfation chemistry, limited thiol availability, and decreased glutathione (GSH) reserve capacity, resulting in a compromised oxidation/reduction (redox) and detoxification capacity. Research indicates that the availability of thiols, particularly GSH, can influence the effects of thimerosal (TM) and other mercury (Hg) compounds.
The purpose of the present critical review is provide mechanistic insight regarding how limited thiol availability, abnormal sulfation chemistry, and decreased GSH reserve capacity in children with an ASD could make them more susceptible to the toxic effects of TM routinely administered as part of mandated childhood immunization schedules."
Click here to read the entire study by scientists at the University of Kentucky and their team, published in August, 2013 in the "International Journal of Environmental Research and Public Health."
"We studied the effects of thimerosal on cell proliferation and mitochondrial function.
B-cells were grown with increasing levels of thimerosal. A subpopulation... showed thimerosal hypersensitivity, whereas none of the control individuals displayed this response.
Cells hypersensitive to thimerosal also had higher levels of oxidative stress markers, protein carbonyls, and oxidant generation.
This suggests certain individuals with a mild mitochondrial defect may be highly susceptible to mitochondrial specific toxins like the vaccine preservative thimerosal."
Click here to read the findings of a team of neurologists in the Department of Neurosurgery, The Methodist Neurological Institute in Houston, Texas. They published their work in June, 2013 in the "Journal of Toxicology."
"Cultured lymphocytes challenged with zinc responded with an impressive up-regulation of MT transcripts (at least nine different MTs were over-expressed) while cells challenged with thimerosal responded by up-regulating numerous heat shock protein transcripts, but not MTs.
The differences in expression profiles between those cells treated with zinc versus thimerosal were dramatic."
Click here to read the abstract of the study by researchers at Wake Forest University. It was published in September, 2006 in the journal, "Neurotoxicology."
"A careful review of ASD cases discloses a number of events that adhere to an immunoexcitotoxic mechanism. This mechanism explains the link between excessive vaccination, use of aluminum and ethylmercury as vaccine adjuvants, food allergies, gut dysbiosis, and abnormal formation of the developing brain.
It has now been shown that chronic microglial activation is present in autistic brains from age 5 years to age 44 years. A considerable amount of evidence, both experimental and clinical, indicates that repeated microglial activation can initiate priming of the microglia and that subsequent stimulation can produce an exaggerated microglial response that can be prolonged. It is also known that one phenotypic form of microglia activation can result in an outpouring of neurotoxic levels of the excitotoxins, glutamate and quinolinic acid. Studies have shown that careful control of brain glutamate levels is essential to brain pathway development and that excesses can result in arrest of neural migration, as well as dendritic and synaptic loss.
It has also been shown that certain cytokines, such as TNF-alpha, can, via its receptor, interact with glutamate receptors to enhance the neurotoxic reaction.
To describe this interaction I have coined the term immunoexcitotoxicity, which is described in this article."
Click here to read the abstract by a Neurosurgeon and professor at Belhaven College in Jackson, Mississippi. It was published in November, 2008.
Click here to read a short examination of the role of mercury in the pathogenesis of autism. It was published in 2002 in the journal, "Molecular Psychiatry."
Thimerosal is a vaccine antimicrobial preservative which has long been suspected an iatrogenic factor possibly contributing to neurodevelopmental disorders including autism.
Thimerosal-treated mice exhibited neural development delay, social interaction deficiency, and inclination of depression. Apparent neuropathological changes were also observed in adult mice neonatally treated with thimerosal.
High-throughput RNA sequencing of autistic-behaved mice brains revealed the alternation of a number of canonical pathways involving neuronal development, neuronal synaptic function, and the dysregulation of endocrine system. Intriguingly, the elevation of anterior pituitary secreting hormones occurred exclusively in male but not in female thimerosal-treated mice, demonstrating for the first time the gender bias of thimerosal-mercury toxicity with regard to endocrine system.
Click here to read the entire study conducted at the Chinese Academy of Sciences and published in June, 2014 in the journal, "Toxicological Sciences."
Click here to read the abstract of the review published in October, 2008 in the "Indian Journal of Medical Research."
"Several recent studies suggest that children diagnosed with an ASD have abnormal sulfation chemistry, limited thiol availability, and decreased glutathione (GSH) reserve capacity, resulting in a compromised oxidation/reduction (redox) and detoxification capacity. Research indicates that the availability of thiols, particularly GSH, can influence the effects of thimerosal (TM) and other mercury (Hg) compounds.
The purpose of the present critical review is provide mechanistic insight regarding how limited thiol availability, abnormal sulfation chemistry, and decreased GSH reserve capacity in children with an ASD could make them more susceptible to the toxic effects of TM routinely administered as part of mandated childhood immunization schedules."
Click here to read the entire study by scientists at the University of Kentucky and their team, published in August, 2013 in the "International Journal of Environmental Research and Public Health."
"We studied the effects of thimerosal on cell proliferation and mitochondrial function.
B-cells were grown with increasing levels of thimerosal. A subpopulation... showed thimerosal hypersensitivity, whereas none of the control individuals displayed this response.
Cells hypersensitive to thimerosal also had higher levels of oxidative stress markers, protein carbonyls, and oxidant generation.
This suggests certain individuals with a mild mitochondrial defect may be highly susceptible to mitochondrial specific toxins like the vaccine preservative thimerosal."
Click here to read the findings of a team of neurologists in the Department of Neurosurgery, The Methodist Neurological Institute in Houston, Texas. They published their work in June, 2013 in the "Journal of Toxicology."
"Cultured lymphocytes challenged with zinc responded with an impressive up-regulation of MT transcripts (at least nine different MTs were over-expressed) while cells challenged with thimerosal responded by up-regulating numerous heat shock protein transcripts, but not MTs.
The differences in expression profiles between those cells treated with zinc versus thimerosal were dramatic."
Click here to read the abstract of the study by researchers at Wake Forest University. It was published in September, 2006 in the journal, "Neurotoxicology."
"A careful review of ASD cases discloses a number of events that adhere to an immunoexcitotoxic mechanism. This mechanism explains the link between excessive vaccination, use of aluminum and ethylmercury as vaccine adjuvants, food allergies, gut dysbiosis, and abnormal formation of the developing brain.
It has now been shown that chronic microglial activation is present in autistic brains from age 5 years to age 44 years. A considerable amount of evidence, both experimental and clinical, indicates that repeated microglial activation can initiate priming of the microglia and that subsequent stimulation can produce an exaggerated microglial response that can be prolonged. It is also known that one phenotypic form of microglia activation can result in an outpouring of neurotoxic levels of the excitotoxins, glutamate and quinolinic acid. Studies have shown that careful control of brain glutamate levels is essential to brain pathway development and that excesses can result in arrest of neural migration, as well as dendritic and synaptic loss.
It has also been shown that certain cytokines, such as TNF-alpha, can, via its receptor, interact with glutamate receptors to enhance the neurotoxic reaction.
To describe this interaction I have coined the term immunoexcitotoxicity, which is described in this article."
Click here to read the abstract by a Neurosurgeon and professor at Belhaven College in Jackson, Mississippi. It was published in November, 2008.
Click here to read a short examination of the role of mercury in the pathogenesis of autism. It was published in 2002 in the journal, "Molecular Psychiatry."
Thimerosal is a vaccine antimicrobial preservative which has long been suspected an iatrogenic factor possibly contributing to neurodevelopmental disorders including autism.
Thimerosal-treated mice exhibited neural development delay, social interaction deficiency, and inclination of depression. Apparent neuropathological changes were also observed in adult mice neonatally treated with thimerosal.
High-throughput RNA sequencing of autistic-behaved mice brains revealed the alternation of a number of canonical pathways involving neuronal development, neuronal synaptic function, and the dysregulation of endocrine system. Intriguingly, the elevation of anterior pituitary secreting hormones occurred exclusively in male but not in female thimerosal-treated mice, demonstrating for the first time the gender bias of thimerosal-mercury toxicity with regard to endocrine system.
Click here to read the entire study conducted at the Chinese Academy of Sciences and published in June, 2014 in the journal, "Toxicological Sciences."
Emmy winning documentary on vaccine induced brain damage: 1982
A documentary from 1982 on pertussis vaccine and brain damage.
Note that the vaccine has been associated with brain damage since it was introduced in 1933.
Also note that before the vaccine was in widespread use deaths from the disease had declined by over 90% since 1930. The decline from the peak in the 19th century was closer to 99%.
Click here to watch fifteen minutes of the documentary on youtube.
Note that the vaccine has been associated with brain damage since it was introduced in 1933.
Also note that before the vaccine was in widespread use deaths from the disease had declined by over 90% since 1930. The decline from the peak in the 19th century was closer to 99%.
Click here to watch fifteen minutes of the documentary on youtube.
Etiology of autism spectrum disorders: Genes, environment, or both?
Dr. Chris Shaw, of the University of British Columbia, is one of the world's foremost authorities on aluminum toxicity.
He and his colleagues review 167 peer reviewed papers, published in the professional literature, on the causes of autism.
They conclude thusly: "Aluminum is both a neurotoxin and an immunotoxin and there is now sufficient evidence from both human and animal studies that cumulative exposure to this adjuvant is not as benign as previously assumed. Because infants represent the most vulnerable population that is universally and routinely exposed to aluminum adjuvants, a more rigorous evaluation of its potentially adverse neurodevelopmental impacts is needed.
Click here to read the entire review.
He and his colleagues review 167 peer reviewed papers, published in the professional literature, on the causes of autism.
They conclude thusly: "Aluminum is both a neurotoxin and an immunotoxin and there is now sufficient evidence from both human and animal studies that cumulative exposure to this adjuvant is not as benign as previously assumed. Because infants represent the most vulnerable population that is universally and routinely exposed to aluminum adjuvants, a more rigorous evaluation of its potentially adverse neurodevelopmental impacts is needed.
Click here to read the entire review.
Theoretical aspects of autism: causes: a review
Dr. Helen Ratajczak, immunologist and retired pharmaceutical senior scientist, reviewed all the literature on autism going back to 1943. She published the results of her study in the January, 2011 issue of the "Journal of Toxicology." She concludes thusly:
"Documented causes of autism include genetic mutations and/or deletions, viral infections, and encephalitis following vaccination."
Click here to read the abstract of her study.
"Documented causes of autism include genetic mutations and/or deletions, viral infections, and encephalitis following vaccination."
Click here to read the abstract of her study.
The Gut and Autism: 28 Studies Confirm Dr. Wakefield's Hypothesis
"The governments conceded or the court ruled that vaccines had caused brain injury. In turn, this injury led to an autism diagnosis. MMR vaccine was the common denominator in these cases."
"Repeated studies from around the world confirmed Wakefield’s finding of bowel disease in autistic children."
"Using sophisticated laboratory methods Dr. Steve Walker and his colleagues endorsed Wakefield’s original findings by showing molecular changes in the children’s intestinal tissues that were highly distinctive and clearly abnormal."
This article includes links to twenty eight studies supporting Wakefield's original hypothesis.
Click here to read the article, then click the links in the footnotes to read the twenty eight studies.
Wakefield was one of thirteen doctors working on the study. They did not claim that vaccines caused autism. They simply noted the temporal relationship. Mostly their study was of the digestive systems of autistic children also suffering from digestive disorders.
Click here to read the study.
Twelve years after it was published, the study was retracted. It was not retracted for scientific reasons or for fraud, or for mistakes or because the findings were invalid or incorrect. It was retracted because of rumors of inconsistencies in the reporting of how study subjects were recruited and for misunderstandings over permissions from the ethics committee.
Click here to read the retraction.
Click here to read about the judicial exoneration of one of the co authors. That scientist had the financial means to pursue legal action while Wakefield did not.
The findings themselves stand, and as the above studies demonstrate, were valid, clinically useful and relevant to treating children so affected.
Click here for links to over ten dozen follow up studies in some way linking vaccines and autism.
"Repeated studies from around the world confirmed Wakefield’s finding of bowel disease in autistic children."
"Using sophisticated laboratory methods Dr. Steve Walker and his colleagues endorsed Wakefield’s original findings by showing molecular changes in the children’s intestinal tissues that were highly distinctive and clearly abnormal."
This article includes links to twenty eight studies supporting Wakefield's original hypothesis.
Click here to read the article, then click the links in the footnotes to read the twenty eight studies.
Wakefield was one of thirteen doctors working on the study. They did not claim that vaccines caused autism. They simply noted the temporal relationship. Mostly their study was of the digestive systems of autistic children also suffering from digestive disorders.
Click here to read the study.
Twelve years after it was published, the study was retracted. It was not retracted for scientific reasons or for fraud, or for mistakes or because the findings were invalid or incorrect. It was retracted because of rumors of inconsistencies in the reporting of how study subjects were recruited and for misunderstandings over permissions from the ethics committee.
Click here to read the retraction.
Click here to read about the judicial exoneration of one of the co authors. That scientist had the financial means to pursue legal action while Wakefield did not.
The findings themselves stand, and as the above studies demonstrate, were valid, clinically useful and relevant to treating children so affected.
Click here for links to over ten dozen follow up studies in some way linking vaccines and autism.
The relationship between correlation and causation: How epidemiologists do it
It is commonly said that, "Correlation does not equal causation" by people who wish to dismiss vaccine injuries as coincidental. They use it as if it means that no two things that are correlated share a causal relationship. This is ridiculous.
To these people, you can reply with the epidemiologists standard reply, "Apply Hill's criteria."
What are Hill's criteria?
"Bradford Hill's criteria are still widely accepted in the modern era as a logical structure for investigating and defining causality in epidemiological study."
In short, they are used to determine when correlation does equal causation. In the case of vaccine injury, they show very clearly that correlation does equal causation.
Click here to read the wikipedia page for Hill's criteria.
To these people, you can reply with the epidemiologists standard reply, "Apply Hill's criteria."
What are Hill's criteria?
"Bradford Hill's criteria are still widely accepted in the modern era as a logical structure for investigating and defining causality in epidemiological study."
In short, they are used to determine when correlation does equal causation. In the case of vaccine injury, they show very clearly that correlation does equal causation.
Click here to read the wikipedia page for Hill's criteria.
Leading Neurosurgeon Analyzes Autism Pandemic
Developmental Fluoride Neurotoxicity: A Systematic Review and Meta-Analysis
"In a meta-analysis, researchers from Harvard School of Public Health
(HSPH) and China Medical University in Shenyang for the first time
combined 27 studies and found strong indications that fluoride may
adversely affect cognitive development in children."
Click here to read the article on Harvard's website about this study.
Their study opens with the line: "A recent report from the National Research Council (NRC 2006) concluded that adverse effects of high fluoride concentrations in drinking water may be of concern." It concludes, "our results support the possibility of adverse effects of fluoride exposures on children’s neurodevelopment."
Click here to read their paper, published in the October, 2012 issue of the journal, "Environmental Health Perspectives."
Click here to read the article on Harvard's website about this study.
Their study opens with the line: "A recent report from the National Research Council (NRC 2006) concluded that adverse effects of high fluoride concentrations in drinking water may be of concern." It concludes, "our results support the possibility of adverse effects of fluoride exposures on children’s neurodevelopment."
Click here to read their paper, published in the October, 2012 issue of the journal, "Environmental Health Perspectives."
Documentary: Silent Epidemic by Dr. Gary Null
This is a brilliant film about the epidemic of vaccine injury. It is chock full of doctors talking about the clinical results, scientists talking about how they work, lawyers describing the legal situation, parents discussing their experience with their injured children and more. It is very thorough and to those who are unfamiliar with the dark side of vaccination it will be an eye opener. It is one hour, forty eight minutes well spent.
Click here to watch the entire documentary on youtube.
Click here to watch the entire documentary on youtube.
Autism: Made in the U.S.A: A documentary by Dr. Gary Null
What does the research say about autism? How is it being cured? Here are the families curing their children of autism, the doctors who are helping them and the scientists who are figuring out how.
Two things really stand out at the end. One is the story one of the mothers tells. Throughout the film we see bits and pieces of the family's journey over the years. Then she talks about telling somebody that her son had been cured of autism and the person replies, "That's impossible." How can people, with a straight face, tell somebody that their experience did not happen?
Another is the list of people at the end of the film. They are people who refused to be interviewed for the film. The positions of power they hold in government and industry would impress some people.
Click here to watch the entire one hour forty minute documentary on youtube.
Two things really stand out at the end. One is the story one of the mothers tells. Throughout the film we see bits and pieces of the family's journey over the years. Then she talks about telling somebody that her son had been cured of autism and the person replies, "That's impossible." How can people, with a straight face, tell somebody that their experience did not happen?
Another is the list of people at the end of the film. They are people who refused to be interviewed for the film. The positions of power they hold in government and industry would impress some people.
Click here to watch the entire one hour forty minute documentary on youtube.
Autism: How close are we to a cure? Dr. Bradstreet lecture
This was one of the world's leading autism doctors. He cured autism, as a number of other doctors, parents and patients have.
Here is a recent lecture he gave, rooted completely in the professional literature and his decades of clinical experience.
His body was found shot and dumped in a river early in the summer of 2015. He had recently been visited by the FBI.
The families he healed and the community that loved him are grieving.
Click here to watch the entire one hour lecture posted on youtube.
Click here to read Dr. Bradstreet's Analysis of the discovery of the brain's immune system and how it relates to autism. It was published in December, 2015 shortly after his death. It was published in the journal, "Frontiers in Neuroscience: Child and Adolescent Psychiatry."
Here is a recent lecture he gave, rooted completely in the professional literature and his decades of clinical experience.
His body was found shot and dumped in a river early in the summer of 2015. He had recently been visited by the FBI.
The families he healed and the community that loved him are grieving.
Click here to watch the entire one hour lecture posted on youtube.
Click here to read Dr. Bradstreet's Analysis of the discovery of the brain's immune system and how it relates to autism. It was published in December, 2015 shortly after his death. It was published in the journal, "Frontiers in Neuroscience: Child and Adolescent Psychiatry."
Aluminum in Vaccines Synergizes with Tylenol to Cause Autism
"Our results provide strong evidence supporting a link between autism and the aluminum in vaccines. A literature review showing toxicity of aluminum in human physiology offers further support."
Click here to read the study by researchers at MIT and others, published in 2012 in the journal, "Entropy."
Click here to read the study by researchers at MIT and others, published in 2012 in the journal, "Entropy."
Brain Damage Discovered in Autistic Children, Absent in Non Autistic Children
"We observed focal patches of abnormal laminar cytoarchitecture and cortical disorganization of neurons, but not glia, in prefrontal and temporal cortical tissue from 10 of 11 children with autism and from 1 of 11 unaffected children."
Click here to read this study by many researchers, published in 2015 in the "New England Journal of Medicine."
Click here to read this study by many researchers, published in 2015 in the "New England Journal of Medicine."