All information containing new and\u00a0unprecedented\u00a0conclusions\u00a0begins by being violently opposed by those who create the prior information and those who subscribe heavily to it. This is very much the case with the link between Autism Spectrum Disorder and vaccines; mainly the MMR vaccine and other thimerosal containing vaccines.<\/p>\n
It is clear that the stance from mainstream science is that there is no link between vaccines and autism. You can find more about that here<\/a>. But for many people this does not dispel all concern. Dr. Hooker, PhD, PE\u00a0<\/b>says that the recent\u00a0U.S. Centers for Disease Control and Prevention\u00a0(CDC)<\/b>\u00a0study on vaccines and autism is\u00a0\u201cperhaps the most flawed and disingenuous study\u201d<\/i>\u00a0he has ever encountered.<\/p>\n Given the number of first hand cases that make their rounds stating that children are immediately affected by certain vaccines and parents are noticing something is \u2018wrong\u2019 suddenly with their child, it is easy to see why people are still concerned. In every vaccine and autism link article we have on CE, there are many comments from parents stating that they watched their child change within hours and days of getting certain vaccines. So is there truly reason to be concerned? Are we just paranoid? Or is there something we have not figured out completely yet?<\/p>\n Regardless of the droves of faithful people hanging onto every word the CDC gives them about the safety of vaccines, I think it is incredibly important that we look at all of the information that truly exists and make our own educated decision. Many claim it is dangerous to question vaccines and I have been threatened on many occasions for writing about it, but it isn\u2019t going to take away the fact that people are being damaged by vaccines. That is a cold hard fact that every parent needs to know about before deciding to vaccinate their child.<\/p>\n The truth is, there have been several court cases where families have been granted damage pay-outs due to what vaccines and their ingredients have done to their children. The cases are directly linked to autism and brain damage. UPDATE:\u00a0<\/b>\u00a0I do feel that even if only a 51% majority in decision is needed, the cases are plaintiff vs. The Secretary of Human Services. If the statement that vaccines had no link to autism was completely factual, these people would not have a case against one entity that would surely have a lot of firepower around the issue. Regardless, their victory illustrates some important factors. In terms of the size of the cases, there are an estimated 5,000 additional cases still awaiting court dates. The reason why it\u2019s much harder and why a class action lawsuit is not possible is because the government inserted a law to protect vaccine makes after they were being forced to pay out billions in damages to families. It came a point where enough was enough when it came to their loss in profit so the gov\u2019t stepped in to assist, unfortunately this isn\u2019t favorable for the people but only business<\/i>.<\/i><\/b><\/p>\n Below I have supplied three links to court cases. Please take the time to check out each one to understand them further.<\/p>\n http:\/\/www.uscfc.uscourts.gov\/sites\/default\/files\/CAMPBELL-SMITH.MOJABI-PROFFER.12.13.2012.pdf<\/a><\/p>\n http:\/\/www.uscfc.uscourts.gov\/sites\/default\/files\/MORAN.LAWSON011211.pdf<\/a><\/p>\n http:\/\/www.uscfc.uscourts.gov\/sites\/default\/files\/CAMPBELLSMITH.%20DOE77082710.pdf<\/a><\/p>\n Is there more evidence linking vaccines to autism? Yes. While some studies exist to state that their is no link between vaccines and autism, I have found several that do show a link. Given the existence of these studies and their results, I think we need to truly examine whether or not vaccines are safe and if it makes sense for us to blindly follow what we are told to do when it comes to vaccines regardless of the dangers. I can already hear the comments that will come in from people stating the dangers of this post and that this is some conspiracy, but it is not. Realize that this is much more of a real and serious issue than many think.<\/p>\n Below is what I have come across in terms of studies thanks to the tireless research of people out there who care about uncovering the truth.<\/p>\n Viral \/ Immune studies:<\/i><\/b><\/p>\n Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in\u00a0children with autism<\/b><\/a><\/p>\n Autoimmunity to the central nervous system (CNS), especially to myelin basic\u00a0protein (MBP), may play a causal role in autism, a neurodevelopmental\u00a0disorder. Because many autistic children harbor elevated levels of measles\u00a0antibodies, we conducted a serological study of measles-mumps-rubella (MMR) and MBP autoantibodies.<\/p>\n \u2026.over 90% of MMR antibody-positive autistic sera were also positive for MBP\u00a0autoantibodies, suggesting a strong association between MMR and CNS\u00a0autoimmunity in autism. Stemming from this evidence, we suggest that an\u00a0inappropriate antibody response to MMR, specifically the measles component Serological association of measles virus and human herpes virus-6\u00a0with brain auto-antibodies in autism<\/b><\/a><\/p>\n This study is the first to report an association between virus serology and\u00a0brain autoantibody in autism; it supports the hypothesis that a virus-induced\u00a0autoimmune response may play a causal role in autism<\/p>\n Hypothesis: conjugate vaccines may predispose children to autism\u00a0spectrum disorders<\/b><\/a><\/p>\n Conjugate vaccines fundamentally change the manner in which the immune\u00a0systems of infants and young children function by deviating their immune\u00a0responses to the targeted carbohydrate antigens from a state of hypo-responsiveness to a robust B2 B cell mediated response.<\/p>\n This period of hypo-responsiveness to carbohydrate antigens coincides with\u00a0the intense myelination process in infants and young children, and conjugate\u00a0vaccines may have disrupted evolutionary forces that favored early brain\u00a0development over the need to protect infants and young children from\u00a0capsular bacteria.<\/p>\n Effects of diphtheria-tetanus-pertussis or tetanus vaccination on\u00a0allergies and allergy-related respiratory symptoms among children<\/b><\/a> The odds of having a history of asthma was twice as great among vaccinated\u00a0subjects than among unvaccinated subjects \u00a0The odds of having had any\u00a0allergy-related respiratory symptom in the past 12 months was 63% greater\u00a0among vaccinated subjects than unvaccinated subjects \u00a0The associations\u00a0between vaccination and subsequent allergies and symptoms were greatest\u00a0among children aged 5 through 10 years.<\/p>\n Neurological Complications of Pertussis Immunization<\/b><\/a><\/p>\n Review is made of 107 cases of neurological complications of pertussis\u00a0inoculation reported in the literature. The early onset of neurological\u00a0symptoms was characteristic, with changes of consciousness and convulsions\u00a0as the most striking features. The question of aetiology is considered and\u00a0contraindications are discussed\u2026.as is the grave danger of further\u00a0inoculations when a previous one has produced any suggestion of a\u00a0neurological reaction.<\/p>\n Hepatitis B vaccination of male neonates and autism diagnosis, NHIS\u00a01997-2002.<\/b><\/a><\/p>\n Findings suggest that U.S. male neonates vaccinated with the hepatitis B\u00a0vaccine prior to 1999 (from vaccination record) had a threefold higher risk for\u00a0parental report of autism diagnosis compared to boys not vaccinated as\u00a0neonates during that same time period. Nonwhite boys bore a greater risk.<\/p>\n Aluminum Studies:<\/i><\/b><\/p>\n Do aluminum vaccine adjuvants contribute to the rising prevalence of\u00a0autism?<\/b><\/a><\/p>\n Our results show that: (i) children from countries with the highest ASD\u00a0prevalence appear to have the highest exposure to Al from vaccines; (ii) the\u00a0increase in exposure to Al adjuvants significantly correlates with the increase\u00a0in ASD prevalence in the United States observed over the last two decades;<\/p>\n and (iii) a significant correlation exists between the amounts of Al administered\u00a0to preschool children and the current prevalence of ASD in seven Western Aluminum hydroxide injections lead to motor deficits and motor\u00a0neuron degeneration.<\/b><\/a><\/p>\n \u2026A second series of experiments was conducted on mice injected with six\u00a0doses of aluminum hydroxide. Behavioural analyses in these mice revealed Aluminum Vaccine Adjuvants: Are they Safe?<\/b><\/a><\/p>\n Experimental research, clearly shows that aluminum adjuvants have a\u00a0potential to induce serious immunological disorders in humans. In particular,\u00a0aluminum in adjuvant form carries a risk for autoimmunity, long-term brain\u00a0inflammation and associated neurological complications and may thus have\u00a0profound and widespread adverse health consequences. \u00a0click for entire study<\/a><\/p>\n Thimerosal studies:<\/i><\/b><\/p>\n Integrating experimental (in vitro and in vivo) neurotoxicity studies of\u00a0low-dose thimerosal relevant to vaccines.<\/b><\/a><\/p>\n There is a need to interpret neurotoxic studies to help deal with uncertainties\u00a0surrounding pregnant mothers, newborns and young children who must\u00a0receive repeated doses of Thimerosal-containing vaccines (TCVs).<\/p>\n Information extracted from studies indicates that: (a) activity of low doses of\u00a0Thimerosal against isolated human and animal brain cells was found in all\u00a0studies and is consistent with Hg neurotoxicity; (b) the neurotoxic effect of\u00a0ethylmercury has not been studied with co-occurring adjuvant-Al in TCVs; (c)\u00a0animal studies have shown that exposure to Thimerosal-Hg can lead to\u00a0accumulation of inorganic Hg in brain, and that (d) doses relevant to TCV\u00a0exposure possess the potential to affect human neuro-development.<\/p>\n Neurodevelopmental disorders following thimerosal-containing\u00a0childhood immunizations: a follow-up analysis<\/b>.<\/a><\/p>\n \u201cThe present study provides additional epidemiological evidence supporting\u00a0previous epidemiological, clinical and experimental evidence that\u00a0administration of thimerosal-containing vaccines in the United States resulted\u00a0in a significant number of children developing NDs.\u201d<\/p>\n Neonatal administration of thimerosal causes persistent changes in\u00a0mu opioid receptors in the rat brain<\/b><\/a><\/p>\n \u201cThese data document that exposure to thimerosal during early postnatal life\u00a0produces lasting alterations in the densities of brain opioid receptors along\u00a0with other neuropathological changes, which may disturb brain development.\u201d<\/p>\n Persistent behavioral impairments and alterations of brain dopamine\u00a0system after early postnatal administration of thimerosal in rats<\/b>.<\/a><\/p>\n \u201cThese data document that early postnatal THIM administration causes lasting\u00a0neurobehavioral impairments and neurochemical alterations in the brain,\u00a0dependent on dose and sex. If similar changes occur in THIM\/mercurial-exposed children, they could contribute do neurodevelopmental disorders.\u201d<\/p>\n Maternal Thimerosal Exposure Results in Aberrant Cerebellar\u00a0Oxidative Stress, Thyroid Hormone Metabolism, and Motor Behavior Thimerosal exposure also resulted in a significant increase in cerebellar levels\u00a0of the oxidative stress marker 3-nitrotyrosine\u2026. This coincided with an\u00a0increased (47.0%) expression of a gene negatively regulated by T3,\u2026 Our\u00a0data thus demonstrate a negative neurodevelopmental impact of perinatal\u00a0thimerosal exposure.<\/p>\n
\nthereof, might be related to pathogenesis of autism.<\/p>\n
\n<\/a><\/b>and adolescents in the United States.<\/b><\/a><\/p>\n
\ncountries, particularly at 3-4 months of age.<\/p>\n
\nsignificant impairments in a number of motor functions as well as diminished\u00a0spatial memory capacity.<\/p>\n
\nin Rat Pups; Sex- and Strain-Dependent Effects.<\/b><\/a><\/p>\n