Vaccine News – “It took me 7 years to teach him how to chew”

Big Pharma is the biggest, baddest, most dangerous drug dealer in the world.

Study – Clinical clues for autoimmunity and neuroinflammation in patients with autistic regression.
RESULTS:
The charts of 206 children with ASD and 33 diagnosed with autistic regression variant were reviewed. The incidence of febrile illness in the 6 months prior to initial parental concern was significantly higher in the children with autistic regression compared with those with ASD (30% vs 0%; p<0.001). The overall prevalence of familial autoimmunity was also higher in children with autistic regression compared with those with ASD (33% vs 12%; p<0.001). Type 1 diabetes and autoimmune thyroiditis were both more common in families with children with autistic regression. Other non-immune risk factors did not differ between the two groups.
INTERPRETATION:
Our findings suggest that predisposition to autoimmunity, and immune/inflammatory activation, may be associated with autistic regression.

The Vaccine Science Contradiction
The modern human race has been thriving and evolving for at least the last 200,000 years according to Anthropologists. Vaccines have only been around for less than 200 years. So how did humans survive for the 199,800 years before that. The answer is that you are born with a fully functioning immune system, capable of self-immunization. Vaccines are not required for immunization. Your body does it automatically. Just like 10,000 generations of your ancestors who also survived without vaccines. If your immune system didn’t work automatically to keep you alive then you would have never been born.

The Amazing Dr. Franz from Orlando.
#gooddoctor #pediatrician #vaxxed #praybig

Episode 7 of The Truth About Vaccines is NOW PLAYING. Tonight’s episode is all about Vaccine alternatives and Freedom of Choice. Super important for you to see.

Aluminium Adjuvants Have Never Been Approved For Use In Vaccination
In a press release, describing Professor Exley’s latest paper, the founder of the Dwoskin Family Foundation, Mrs. Claire Dwoskin wrote:
“Research at Keele University led by Professor Christopher Exley aims to understand the toxicity of aluminum adjuvants in vaccinations and their latest findings are now published in Nature’s ‘Scientific Reports.
In a project funded by the Medical Research Council (MRC) and the Dwoskin Foundation the group at Keele investigated the relationship between the physicochemical properties of aluminum adjuvants and the immune response. Specifically, they show that the reaction of the aluminum adjuvant at the injection site will determine its subsequent fate and therefore its activity both at the injection site and away from the injection site.
One form of aluminum adjuvant which is most commonly used in vaccines is an aluminum hydroxyphosphate salt and is more toxic at the injection site than the second form of aluminum adjuvant, also commonly used in vaccines, aluminum oxyhydroxide salt. However, the latter is more easily loaded into immune reactive cells with the possibility to be transported throughout the body. It is suggested by the Keele research that this loading of aluminum into viable cells offers a mechanism whereby significant amounts of aluminum, a known neurotoxin, might be translocated throughout the body and even across the blood brain barrier and into the central nervous system.” [2, 3, 4]
Countless Childhood Vaccinations Contain Aluminum

Shingles Vaccine Zostavax Is Causing What It’s Designed To Prevent
April 19, 2017
By now I think most people have seen the commercials on television telling us that if we’ve ever had the chicken pox at any point in our lives, then the shingles virus is already inside of us. As it stands right now, there is a vaccine for shingles called Zostavax, but what we’re finding out now about this vaccine makes it seem like it might be pretty dangerous or at least cause some side effects that are actually the same as what we’d see from shingles. Ring of Fire’s Farron Cousins talks with Attorney Troy Bouk about the dangers associated with Zostavax

Dying 13 Year Old Diagnoses Her Own HPV Vaccine Injury that Stumped Doctors
April 20, 2017
Health Impact News Editor Comments
One of the true tragedies in modern medicine is the refusal to consider vaccine injuries when diagnosing or treating disease. The U.S. government acknowledges that people die and are injured by vaccines, as is evidenced from the Department of Justice’s quarterly reports on settlements in vaccine court: http://vaccineimpact.com/vaccine-injuries-and-deaths-compensated-through-vaccine-court/
However, medical students are given no training in recognizing or treating vaccine injuries, and no studies are ever conducted to find out why some children suffer from vaccines while others do not.
In this story out of the U.K., a 13 year old girl accomplishes something her doctors could not do, and that was diagnose her own life-threatening disease by researching all of the possibilities, without excluding vaccine injuries, something that apparently handicapped her doctors. She discovered that she suffered from an autoimmune disease after receiving the HPV vaccine.

Professor Hamamoto talks about the persecution he faces at UC Davis after speaking the truth to his students. #Vaxxed #DarrylHamamoto #SenatorPan #SB277 #OperationPaperClip
Camera, editing and sound by Joshua Coleman.
YOUTUBE:

It took me 7 years to teach him how to chew
Nancy Kirkman’s son was severely injured by vaccines at 3 months of age. The family has been subjected to immense heartache and cruelty.
Interview recorded on February 2, 2017 in San Diego, California.
YOUTUBE LINK:

#VaxxedNation #VaxxedNationTour #RFKcommission #Truth #Science #Vaxxed #Tears #VaxxedTears

Baby’s Health Rapidly Declines After Receiving 13 Vaccines at One Time – Mom Accused of Abuse for Disagreeing with Doctors
April 20, 2017
Durenda and her son KJ on his 1st birthday, before he had 8 shots in one day.
by Health Impact News/MedicalKidnap.com Staff
A young Georgia mother had no idea that a routine trip to the pediatrician’s office for her son’s 1 year check-up would change her son’s life forever, and leave her fighting the state for custody of her own son. When the nurse-practitioner told her that her son was a little behind on his shots and they would need to catch up, Durenda Whitehead didn’t question the need for the vaccines. She did, however, question the safety of giving 13 vaccines at once.
Durenda’s pediatrician assured her that it was fine:
I can give up to 20 at one time.
Durenda was unaware of a research study published in the summer 2016 edition of the Journal of American Physicians and Surgeons by Neil Z. Miller entitled, “Combining Childhood Vaccines at One Visit Is Not Safe.” In a press release, Miller wrote:
Our study showed that infants who receive several vaccines concurrently…are significantly more likely to be hospitalized or die when compared with infants who receive fewer vaccines simultaneously.
Baby’s Health Declines After 13 Vaccines in One Day
During his first year of life, little KJ had a few bouts with respiratory illness, but on January 16, 2017, he was healthy, happy, and active.

Study – Combining Childhood Vaccines at One Visit Is Not Safe
Neil Z. Miller

#VaXism NEWS
#Texas Well done Texans For Vaccine Choice!!
Thank you freedom Reps!
Zedler let TIP have it!!
#HB2249

Skip that Newborn Vitamin K Shot
How much synthetic vitamin K is in the shot? Shockingly, the national standard mandated by most states for US hospitals to administer is over 100 times the infant’s RDA of this nutrient. Since studies have linked large doses of vitamin K with childhood cancers and leukemia, this large dose of synthetic K administered within minutes of birth seems questionable at best.
The fact is that medical science still does not know that much about the metabolic fate of vitamin K. Little to no unmetabolized vitamin K shows up in urine or bile. This is disturbing given the fact that vitamin K is a fat soluble vitamin and therefore has the potential to accumulate in body tissues. More disturbing is that the liver of a newborn does not begin to function until 3 or 4 days after birth. As a result, this little being has very limited to no ability to detoxify the large dose of synthetic vitamin K and all other the dangerous ingredients in the injection cocktail including:

– Phenol (carbolic acid – a poisonous substance derived from coal tar)
– Benzyl alcohol (preservative)
– Propylene glycol (better known as “edible” antifreeze)
– Acetic acid (astringent, antimicrobial agent)
– Hydrochloric acid
– Lecithin
– Castor oil

The manufacturer’s insert included with the shot includes the following warning:
Severe reactions, including fatalities, have occurred during and immediately after intravenous injection of phytonadione [synthetic Vitamin K] even when precautions have been taken to dilute the vitamin and avoid rapid infusion ….
The manufacturer’s insert is no exaggeration of the risks. On October 17, 2013, a case of anaphylactic shock in a newborn from the synthetic vitamin K shot was reported making the possibility of death from this shot a a very real side effect
Source:
Anaphylactic shock due to vitamin K in a newborn and review of literature
Abstract
Newborn infants are born with an immature innate immunity. They are less likely to develop anaphylaxis since their immune system is weaker than older infants and children. There are only a few reports of side effects after vitamin K injection in neonates although prophylaxis against hemorrhagic disease of the newborn with this drug has been in routine practice in all over the world for many years. We herein report a case of anaphylactic shock developing after the intramuscular administration of vitamin K1 in a newborn. To our knowledge, this patient is the first case of neonatal anaphylactic shock developing due to intramuscular administration of vitamin K1. We suggest the clinicians should be aware of this possibility of potentially fatal adverse effect occurring with intramuscular administration of vitamin K1.
Does this make any sense to you? It makes absolutely no sense to me. How could anyone say that this shot is safe and effective for newborns?

Is There Vaccine Cause-And-Correlation Regarding The Dramatic Rise In Children’s Chronic Diseases?
Posted on April 18, 2017
Since the introduction of CDC’s hyper-vaccine schedule, which saw children’s vaccines schedules increase from 10 to 69 vaccines after the 1986  National Childhood Vaccine Injury Act was passed into law, very young children are contracting chronic “old age type” diseases early in life—an anomaly heretofore not experienced demographically.
First off, obesity rates (2013-2014) for U.S. children between the ages of 6 and 11 years was 17.4% [1]  Three leading causes of death in children between 1 and 4 years of age were congenital malformations, deformations and chromosomal abnormalities. [1]   Mandatory pregnancy vaccines have impact upon growing fetuses.  For children 5 to 14 years of age, it’s cancer! [1]   However, according to Contemporary Pediatrics [2] 2014 published data, cancer was the second leading cause of death for children between 1 and 9 years of age (11.8% of deaths).  For infants, the third leading cause of death was sudden infant death syndrome (SIDS, 8.4%)—something that seemingly appeared in pediatric medicine context concomitantly with the increase in mandated vaccines, specifically with multi-valent vaccines, i.e., numerous vaccines given at one time.  However, the CDC’s information about SIDS claims vaccines do not cause SIDS.  Try telling that to many parents.
According to Focus for Health, 27% of U.S. children live with chronic diseases! [3]   That website asks the question, “Why are today’s children sicker than ever before?”  The answer: “While genes may play a role in obesity, asthma and ADHD, environmental and social changes are behind the surge, researchers said.”5 [Children Sicker Now Than in Past, Harvard Report Says] [4]   That Harvard Report found a fourfold increase in childhood obesity; twice the asthma rate since the 1980s; and regarding diabetes: White children’s rate was 26.1 per 100,000; black children, 25.4 per 100,000; American Indian youth, 25 per 100,000 including the highest rate of type-2 diabetes. [4] According to the CDC, one in six children in the USA has a developmental disability, which represents a 17% rise between 1997 and 2008. [7]
Furthermore, are you aware the cost of fully vaccinating a child has increased by 2,700% during the last decade?  Vaccines are extremely profitable for manufacturers, but very costly in terms of adverse health effects, medical bills for parents, and social issues (day care, school, jobs, welfare benefits, etc.) for infants, toddlers, teens and adults.

The Dangers Of Vaccines and Vaccination
Vaccines Are Unavoidably Unsafe
According to the US Food and Drug Administration, safety assessments for vaccines have not often included toxicity studies because vaccines have not been viewed as inherently toxic. Yet vaccines are legally defined as unavoidably unsafe.
It is not just childhood vaccines that come with substantial risk. Influenza vaccines, vaccines for sexually transmitted diseases, and others contain similar risks for adverse events. Also troubling is that vaccination is recommended now for pregnant women, even though vaccine package inserts clearly state they have not been tested on pregnant women, so the effects on the fetus can’t be known.
In the 1960s only a handful of childhood vaccines were given. The current CDC recommended vaccine schedule for children now has over 30 vaccines by the time a child turns 6 and an additional potential for up to 30 more by the time they reach 18. Could this increase be linked to our declining health? For example, currently:

    One in six children in the US has a learning disability
Over 50% suffer from some type of chronic illness.
Cancer is the leading cause of death in our children
Autism rates have soared from 1 in 10,000 in 1990 to 1 in 68 today

Since genetic mutations change slowly over generations, we must look to environmental causes for these changes. While other environmental toxins certainly are at play in these statistics, disregarding the potential role to the amounts of toxin injected into children through vaccines is not only bad public policy, it is bad science. By disregarding the role of vaccines in our statistics for infant mortality and chronic diseases, we could be doing more harm than good in mandating, or even advising, them.
Vaccine Adverse Effects: Known Risks
The list of adverse side effects for vaccines is long and troubling. A quick scan of the Vaccine Injury Table kept by the Health Resource Center for the U.S. Department of Health and Human Services reveals that compensation for injury is possible from a variety of the most common vaccines given to children.
Adverse events are the reason the Vaccine Injury Compensation Program has paid out over 3 billion dollars from 1988 – 2016 despite the fact that only 1 in 5 claims receives any compensation at all. Studies reveal that a small fraction of those injured by vaccines ever file any claim at all since most doctors reject the notion that a problem was caused by a vaccine despite the reality that such problems are listed on the manufacturers product insert. You can learn more by reading this fficial document: National Vaccine Injury Compensation Program.
Vaccines: Adverse Effects List
Various vaccines are linked to the following serious adverse reactions:

    Anaphylactic shock
Aseptic meningitis, meningitis
Bell’s palsy, facial palsy, isolated cranial nerve palsy
Blood disorders such as thrombocytopenic purpura (a disease that destroys platelets need for clotting)
Brachial neuritis
Cerebrovascular accident (stroke)
Chronic rheumatoid arthritis
Convulsions, seizures, febrile seizure
Death
Encephalopathy and encephalitis (brain swelling)
Hearing loss
Guillain-Barré syndrome
Immune system disorders
Lymphatic system disorders
Multiple sclerosis
Myocarditis
Nervous system disorders
Neurological syndromes including autism
Paralysis and myelitis including transverse myelitis
Peripheral neuropathy
Pneumonia and lower respiratory infections
Skin and tissue disorders including eczema
Sudden infant death syndrome (SIDS)
Tinnitus (ringing in the ears)
Vaccine-strain versions of chicken pox, measles, mumps, polio, influenza, meningitis, yellow fever, and pertussis
Vasculitis (inflammation of blood vessels)

 

 

Sunny Irby Polito’s twins, Luke and Campbell, both regressed after receiving MMR and several other vaccinations concurrently at their 12-month “well baby” visit

Vaccine injury testiony –  Sunny Irby Polito’s twins, Luke and Campbell, both regressed after receiving MMR and several other vaccinations concurrently at their 12-month “well baby” visit.
“They just blew up in a GI sort of way…12-15 diapers a day for each of them”

300 pages of study abstracts culled directly from the National Library of Medicine’s pubmed.gov

GreenMedInfo.com has painstakingly collected over 300 pages of study abstracts culled directly from the National Library of Medicine’s pubmed.gov bibliographic database on the wide-ranging adverse health effects linked to vaccines in the today’s schedule (over 200 distinct adverse effects, including death), as well as numerous studies related to vaccine contamination, and vaccine failure in highly vaccine compliant populations.
1. Hepatitis B Vaccination of Male Neonates and Autism Annals of Epidemiology, September 2009 CM Gallagher, MS Goodman, Stony Brook University Medical CenterBoys vaccinated as neonates had threefold greater odds for autism diagnosis compared to boys never vaccinated or vaccinated after the first month of life.
2. Porphyrinuria in childhood autistic disorder: Implications for environmental toxicity Toxicology and Applied Pharmacology, 2006 Robert Natafa, et al, Laboratoire Philippe Auguste, Paris, France These data implicate environmental toxicity in childhood autistic disorder.
3. Theoretical aspects of autism: Causes—A review Journal of Immunotoxicology, January-March 2011 Helen V. Ratajczak, PhD 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.
4. Uncoupling of ATP-mediated Calcium Signaling and Dysregulated IL-6 Secretion in Dendritic Cells by Nanomolar Thimerosal Environmental Health Perspectives, July 2006. Samuel R. Goth, Ruth A. Chu Jeffrey P. Gregg This study demonstrates that very low-levels of Thimerosal can contribute to immune system disregulation.
5. Gender-selective toxicity of thimerosal Exp Toxicol Pathol. 2009 Mar;61(2):133-6. Epub 2008 Sep 3. Branch DR, Departments of Medicine and Laboratory Medicine and Pathobiology, University of Toronto A recent report shows a correlation of the historical use of thimerosal in therapeutic immunizations with the subsequent development of autism; however, this association remains controversial. Autism occurs approximately four times more frequently in males compared to females; thus, studies of thimerosal toxicity should take into consideration gender-selective effects. The present study was originally undertaken to determine the maximum tolerated dose (MTD) of thimersosal in male and female CD1 mice. However, during the limited MTD studies, it became apparent that thimerosal has a differential MTD that depends on whether the mouse is male or female.
6. Comparison of Blood and Brain Mercury Levels in Infant monkeys exposed to Vaccines Containing Thimerosal Environmental Health Perspectives, Aug 2005. Thomas Burbacher, PhD, University of Washington This study demonstrates clearly and unequivocally that ethyl mercury, the kind of mercury found in vaccines, not only ends up in the brain, but leaves double the amount of inorganic mercury as methyl mercury, the kind of mercury found in fish. This work is groundbreaking because little is known about ethyl mercury, and many health authorities have asserted that the mercury found in vaccines is the “safe kind.” This study also delivers a strong rebuke of the Institute of Medicine’s recommendation in 2004 to no longer pursue the mercury-autism connection.
7. Increases in the number of reactive glia in the visual cortex of Macaca fascicularis following subclinical long-term methyl mercury exposure Toxicology and Applied Pharmacology, 1994 Charleston JS et al, Department of Pathology, School of Medicine, University of Washington The identities of the reactive glial cells and the implications for the long-term function and survivability of the neurons due to changes in the glial population following subclinical long-term exposure to mercury are discussed.
8. Neuroglial Activation and Neuroinflammation in the Brain of Patients with Autism Annals of Neurology, Feb 2005. Diana L. Vargas, MD [Johns Hopkins University] This study, performed independently and using a different methodology than Dr. Herbert (see above) reached the same conclusion: the brains of autistic children are suffering from inflammation.
9. Autism: A Brain Disorder, or a Disorder That Affects the Brain? Clinical Neuropsychiatry, 2005 Martha R. Herbert M.D., Ph.D., Harvard University Autism is defined behaviorally, as a syndrome of abnormalities involving language, social reciprocity and hyperfocus or reduced behavioral flexibility. It is clearly heterogeneous, and it can be accompanied by unusual talents as well as by impairments, but its underlying biological and genetic basis in unknown. Autism has been modeled as a brain-based, strongly genetic disorder, but emerging findings and hypotheses support a broader model of the condition as a genetically influenced and systemic.
10. Activation of Methionine Synthase by Insulin-like Growth Factor-1 and Dopamine: a Target for Neurodevelopmental Toxins and Thimerosal  Molecular Psychiatry, July 2004. Richard C. Deth, PhD [Northeastern University] This study demonstrates how Thimerosal inhibits methylation, a central driver of cellular communication and development.
11. Validation of the Phenomenon of Autistic Regression Using Home Videotapes Archives of General Psychiatry, 2005 Emily Werner, PhD; Geraldine Dawson, PhD, University of WashingtonConclusion This study validates the existence of early autistic regression.
12. Blood Levels of Mercury Are Related to Diagnosis of Autism: A Reanalysis of an Important Data Set Journal of Child Neurology, 2007 M. Catherine DeSoto, PhD, Robert T. Hitlan, PhD -Department of Psychology, University of Northern Iowa Excerpt: “We have reanalyzed the data set originally reported by Ip et al. in 2004 and have found that the original p value was in error and that a significant relation does exist between the blood levels of mercury and diagnosis of an autism spectrum disorder. Moreover, the hair sample analysis results offer some support for the idea that persons with autism may be less efficient and more variable at eliminating mercury from the blood.”
13. Developmental Regression and Mitochondrial Dysfunction in a Child With Autism Journal of Child Neurology, February 2006 Jon S. Poling, MD, PhD, Department of Neurology and Neurosurgery, Johns Hopkins Hospital Excerpt: “Children who have (mitochondrial-related) dysfunctional cellular energy metabolism might be more prone to undergo autistic regression between 18 and 30 months of age if they also have infections or immunizations at the same time.”
14. Oxidative Stress in Autism: Elevated Cerebellar 3-nitrotyrosine Levels American Journal of Biochemistry and Biotechnology, 2008 Elizabeth M. Sajdel-Sulkowska, – Dept of Psychiatry, Harvard Medical School Excerpt: The preliminary data suggest a need for more extensive studies of oxidative stress, its relationship to the environmental factors and its possible attenuation by antioxidants in autism.”
15. Large Brains in Autism: The Challenge of Pervasive Abnormality The Neuroscientist, 2005. Martha Herbert, MD, PhD, Harvard University This study helps refute the notion that the brains of autistic children are simply wired differently and notes, “neuroinflammation appears to be present in autistic brain tissue from childhood through adulthood.” Dr. Herbert suggests that chronic disease or an external environmental source (like heavy metals) may be causing the inflammation.
16. Evidence of Toxicity, Oxidative Stress, and Neuronal Insult in Autism Journal of Toxicology and Environmental Health, Nov-Dec 2006. Janet Kern, Anne Jones, Department of Psychiatry, University of Texas Southwestern Medical Center “This article discusses the evidence for the case that some children with autism may become autistic from neuronal cell death or brain damage sometime after birth as result of insult; and addresses the hypotheses that toxicity and oxidative stress may be a cause of neuronal insult in autism… the article discusses what may be happening over the course of development and the multiple factors that may interplay and make these children more vulnerable to toxicity, oxidative stress, and neuronal insult.”
17. Oxidative Stress in Autism Pathophysiology, 2006. Abha Chauhan, Ved Chauhan This study provides a helpful overview of the growing evidence supporting the link between oxidative stress and autism.
18. Thimerosal Neurotoxicity is Associated with Glutathione Depletion: Protection with Glutathione Precursors Neurotoxicology, Jan 2005. S. Jill James, PhD, University of Arkansas This recent study demonstrates that Thimerosal lowers or inhibits the body’s ability to produce Glutathione, an antioxidant and the body’s primary cellular-level defense against mercury.
19. Aluminum adjuvant linked to gulf war illness induces motor neuron death in mice Neuromolecular Medicine, 2007 Christopher Shaw, Ph.D., Department of Ophthalmology and Program in Neuroscience, University of British Columbia This study demonstrates the extreme toxicity of the aluminum adjuvant used as a preservative in vaccines.
20. Environmental mercury release, special education rates, and autism disorder: an ecological study of Texas Health & Place, 2006 Raymond F. Palmer, University of Texas Health Science Center This study demonstrated the correlation between environmental mercury and autism rates in Texas.
21. Autism Spectrum Disorders in Relation to Distribution of Hazardous Air Pollutants in the SF Bay Area Environmental Health Perspectives, September, 2006 Gayle Windham, Div. of Environmental and Occupational Disease Control, California Department of Health Services Excerpt: “Our results suggest a potential association between autism and estimated metal concentrations, and possibly solvents, in ambient air around the birth residence.”
22. A Case Series of Children with Apparent Mercury Toxic Encephalopathies Manifesting with Clinical Symptoms of Regressive Autistic Disorder Journal of Toxicology and Environmental Health, 2007 David A. Geier, Mark R. Geier This study reviewed the case histories and medical profiles of nine autistic children and concluded that eight of the nine children were mercury toxic and this toxicity manifested itself in a manner consistent with Autism Spectrum Disorders.
23. Attention-deficit hyperactivity disorder and blood mercury level: a case-control study in chinese children Neuropediatrics, August 2006 – P.R. Kong Excerpt: “There was significant difference in blood mercury levels between cases and controls, which persists after adjustment for age, gender and parental occupational status. The geometric mean blood mercury level was also significantly higher in children with inattentive and combined subtypes of ADHD. High blood mercury level was associated with ADHD. Whether the relationship is causal requires further studies.”
24. The Changing Prevalence of Autism In California Journal of Autism and Developmental Disorders, April 2003 Mark F. Blaxill, David S. Baskin, and Walter O. Spitzer This study helps to refute the supposition made by some researchers that autism’s epidemic may only be due to “diagnostic substitution”.
25. Mitochondrial Energy-Deficient Endophenotype in Autism American Journal of Biochemistry and Biotechnology 2008 J. Jay Gargus and Faiqa Imtiaz, School of Medicine, University of California, Irvine, “While evidence points to a multigenic etiology of most autism, the pathophysiology of the disorder has yet to be defined and the underlying genes and biochemical pathways they subserve remain unknown.”
26. Bridging from Cells to Cognition in Autism Pathophysiology: Biological Pathways to Defective Brain Function and Plasticity American Journal of Biochemistry and Biotechnology 2008 Matthew P. Anderson, Brian S. Hooker and Martha R. Herbert, Cambridge Health Alliance/Harvard Medical School/Beth Israel Deaconess Medical Center “We review evidence to support a model where the disease process underlying autism may begin when an in utero or early postnatal environmental, infectious, seizure, or autoimmune insult triggers an immune response that increases reactive oxygen species (ROS) production in the brain that leads to DNA damage (nuclear and mitochondrial) and metabolic enzyme blockade and that these inflammatory and oxidative stressors persist beyond early development (with potential further exacerbations), producing ongoing functional consequences.”
27. Heavy-Metal Toxicity—With Emphasis on Mercury John Neustadt, ND, and Steve Pieczenik, MD, PhD Conclusion: Metals are ubiquitous in our environment, and exposure to them is inevitable. However, not all people accumulate toxic levels of metals or exhibit symptoms of metal toxicity, suggesting that genetics play a role in their potential to damage health.
28. Evidence of Mitochondrial Dysfunction in Autism and Implications for Treatment American Journal of Biochemistry and Biotechnology Daniel A. Rossignol, J. Jeffrey Bradstreet MtD and oxidative stress may also explain the high male to female ratio found in autism due to increased male vulnerability to these dysfunctions.
29. Proximity to point sources of environmental mercury release as a predictor of autism prevalence
Health & Place, 2008 Raymond F. Palmer et al, University of Texas Health Science Center This study should be viewed as hypothesis-generating – a first step in examining the potential role of environmental mercury and childhood developmental disorders. Nothing is known about specific exposure routes, dosage, timing, and individual susceptibility. We suspect that persistent low-dose exposures to various environmental toxicants, including mercury, that occur during critical windows of neural development among genetically susceptible children (with a diminished capacity for metabolizing accumulated toxicants) may increase the risk for developmental disorders such as autism.
30. Epidemiology of autism spectrum disorder in Portugal: prevalence, clinical characterization, and medical conditions Developmental Medicine & Child Neurology, 2007 Guiomar Oliveira MD PhD et al, Centro de Desenvolvimento da Criança, Hospital Pediátrico de Coimbra; Assunção Ataíde BSc, Direcção Regional de Educação do Centro Coimbra; The objective of this study was to estimate the prevalence of autistic spectrum disorder (ASD) and identify its clinical characterization, and medical conditions in a paediatric population in Portugal.

Vaccines have NEVER been proven safe

Recent post from LearnTheRisk.org founder and ex-pharmaceutical rep Brandy Vaughan in response to a comment that said: vaccines have “saved” millions of lives, been proven safe and have no side effects.
Brandy Vaughan: “Vaccines have NEVER been proven safe because that would take studies that are ethically done from independent researchers not paid by Pharma. That would require real placebo-based long term, combination studies, which have NEVER been done. Vaccines have not saved MILLIONS of lives, even the CDC credits chlorinated water with the decline of infectious disease deaths that happened well before the vaccine program was established.
Also, if vaccines “saved” us then we would all be dead of TB, cholera and pneumonia because those were three top killers in the early 1900s and there was NO widespread vaccine program for these diseases, yet they disappeared due to increased sanitation, indoor plumbing and better access to food in overcrowded cities.
And as for side effects, check the vaccine inserts themselves — have you seen one lately? Because they list neurological damage and issues, autoimmune issues, nervous system damage, death, etc, on the product insert. All pharmaceutical products have side effects and vaccines have even more serious ones because the toxic additives — including known neurotoxins and known cancer-causing chemicals — are far more potent when injected versus ingested.
And we have the sickest generation of children with nearly half having a chronic issue — we are NOT “fine”. Skyrocketing rates of autoimmune issues — think allergies, type-1 diabetes, lupus, CFS, MS, asthma, psoriasis, arthritis — and neurological damage such as developmental delays, autism, epilepsy, tics, ADHD, Alzheimer’s, etc. We have the highest infant mortality rate and first-day death rate of babies in the developed world — even though we spend more per capita on “health”care than any other developed country. These are facts.
So I ask you to actually open your mind because we are all being lied to — and many children and adults are suffering the consequences of a system that is focused on keeping us sick, not healthy.”