Courts Rule Vaccines Containing MMR and Thimerosal Caused Autism and Brain Damage

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toxic-vaccine-dees

All information containing new and unprecedented conclusions begins 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.

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. But for many people this does not dispel all concern. Dr. Hooker, PhD, PE says that the recent U.S. Centers for Disease Control and Prevention (CDC) study on vaccines and autism is “perhaps the most flawed and disingenuous study” he has ever encountered.

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 ‘wrong’ 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?

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’t 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.

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, and each injury has been deemed ’caused by vaccines.’ Below I have supplied three links to court cases. Please take the time to check out each one to understand them further.

http://www.uscfc.uscourts.gov/sites/default/

http://www.uscfc.uscourts.gov/sites/default/

http://www.uscfc.uscourts.gov/sites/default/

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.

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.

Viral / Immune studies:

Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism

Autoimmunity to the central nervous system (CNS), especially to myelin basic protein (MBP), may play a causal role in autism, a neurodevelopmental disorder. Because many autistic children harbor elevated levels of measles antibodies, we conducted a serological study of measles-mumps-rubella
(MMR) and MBP autoantibodies.

….over 90% of MMR antibody-positive autistic sera were also positive for MBP autoantibodies, suggesting a strong association between MMR and CNS autoimmunity in autism. Stemming from this evidence, we suggest that an inappropriate antibody response to MMR, specifically the measles component
thereof, might be related to pathogenesis of autism.

Serological association of measles virus and human herpes virus-6 with brain auto-antibodies in autism

This study is the first to report an association between virus serology and brain autoantibody in autism; it supports the hypothesis that a virus-induced autoimmune response may play a causal role in autism

Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders

Conjugate vaccines fundamentally change the manner in which the immune systems of infants and young children function by deviating their immune responses to the targeted carbohydrate antigens from a state of hypo-responsiveness to a robust B2 B cell mediated response.

This period of hypo-responsiveness to carbohydrate antigens coincides with the intense myelination process in infants and young children, and conjugate vaccines may have disrupted evolutionary forces that favored early brain development over the need to protect infants and young children from capsular bacteria.

Effects of diphtheria-tetanus-pertussis or tetanus vaccination on allergies and allergy-related respiratory symptoms among children
and adolescents in the United States.

The odds of having a history of asthma was twice as great among vaccinated subjects than among unvaccinated subjects  The odds of having had any allergy-related respiratory symptom in the past 12 months was 63% greater among vaccinated subjects than unvaccinated subjects  The associations between vaccination and subsequent allergies and symptoms were greatest among children aged 5 through 10 years.

Neurological Complications of Pertussis Immunization

Review is made of 107 cases of neurological complications of pertussis inoculation reported in the literature. The early onset of neurological symptoms was characteristic, with changes of consciousness and convulsions as the most striking features. The question of aetiology is considered and contraindications are discussed….as is the grave danger of further inoculations when a previous one has produced any suggestion of a neurological reaction.

Hepatitis B vaccination of male neonates and autism diagnosis, NHIS 1997-2002.

Findings suggest that U.S. male neonates vaccinated with the hepatitis B vaccine prior to 1999 (from vaccination record) had a threefold higher risk for parental report of autism diagnosis compared to boys not vaccinated as neonates during that same time period. Nonwhite boys bore a greater risk.

Aluminum Studies:

Do aluminum vaccine adjuvants contribute to the rising prevalence of autism?

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;

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.

Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration.

…A second series of experiments was conducted on mice injected with six doses of aluminum hydroxide. Behavioural analyses in these mice revealed
significant impairments in a number of motor functions as well as diminished spatial memory capacity.

Aluminum Vaccine Adjuvants: Are they Safe?

Experimental research, clearly shows that aluminum adjuvants have a potential to induce serious immunological disorders in humans. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications and may thus have profound and widespread adverse health consequences.  click for entire study

Thimerosal studies:

Integrating experimental (in vitro and in vivo) neurotoxicity studies of low-dose thimerosal relevant to vaccines.

There is a need to interpret neurotoxic studies to help deal with uncertainties surrounding pregnant mothers, newborns and young children who must receive repeated doses of Thimerosal-containing vaccines (TCVs).

Information extracted from studies indicates that: (a) activity of low doses of Thimerosal against isolated human and animal brain cells was found in all studies and is consistent with Hg neurotoxicity; (b) the neurotoxic effect of ethylmercury has not been studied with co-occurring adjuvant-Al in TCVs; (c) animal studies have shown that exposure to Thimerosal-Hg can lead to accumulation of inorganic Hg in brain, and that (d) doses relevant to TCV exposure possess the potential to affect human neuro-development.

Neurodevelopmental disorders following thimerosal-containing childhood immunizations: a follow-up analysis.

“The present study provides additional epidemiological evidence supporting previous epidemiological, clinical and experimental evidence that administration of thimerosal-containing vaccines in the United States resulted in a significant number of children developing NDs.”

Neonatal administration of thimerosal causes persistent changes in mu opioid receptors in the rat brain

“These data document that exposure to thimerosal during early postnatal life produces lasting alterations in the densities of brain opioid receptors along with other neuropathological changes, which may disturb brain development.”

Persistent behavioral impairments and alterations of brain dopamine system after early postnatal administration of thimerosal in rats.

“These data document that early postnatal THIM administration causes lasting neurobehavioral impairments and neurochemical alterations in the brain, dependent on dose and sex. If similar changes occur in THIM/mercurial-exposed children, they could contribute do neurodevelopmental disorders.”

Maternal Thimerosal Exposure Results in Aberrant Cerebellar Oxidative Stress, Thyroid Hormone Metabolism, and Motor Behavior
in Rat Pups; Sex- and Strain-Dependent Effects.

Thimerosal exposure also resulted in a significant increase in cerebellar levels of the oxidative stress marker 3-nitrotyrosine…. This coincided with an increased (47.0%) expression of a gene negatively regulated by T3,… Our data thus demonstrate a negative neurodevelopmental impact of perinatal thimerosal exposure.

Administration of thimerosal to infant rats increases overflow of glutamate and aspartate in the prefrontal cortex: protective role of
dehydroepiandrosterone sulfate.

Thimerosal, a mercury-containing vaccine preservative, is a suspected factor in the etiology of neurodevelopmental disorders. We previously showed that its administration to infant rats causes behavioral, neurochemical and neuropathological abnormalities similar to those present in autism.

Sources:

http://healthimpactnews.com/2013/can-we-trust-the-cdc-claim-that-there-is-no-link-between-vaccines-and-autism/

http://www.regardingcaroline.com/pubmed

http://www.jpeds.com/content/JPEDSDeStefano

Joe Martino

Hey! You are currently engaged in what I’m passionate about, Collective Evolution. I created CE 4 years ago and have been heavily at it since. I love inspiring others to make change and am excited to play an active role in making this all happen. I’ve been researching much of the content I share for about 7 years and apply the same wisdom I share to others to my own life. Hands down the only other thing I am this passionate about is baseball. Feel free to email me at joe@collective-evolution.com

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  • BubbaT

    If you get any vaccine or have your children take any vaccine you’re an idiot.

    • Barn Cat

      No, if you don’t get vaccinated for the big 6 childhood diseases like polio you should go to jail for child endangerment.

  • Evie

    Just wondering why? In the 50s, 60s and 70s there was no altism and not even much add. Not only do we have to support the corporations but they make people sick too.

    • Barn Cat

      We had vaccinations back then too didn’t we???

      • mama bear

        Yes, there were vaccines. Diagnosis for stuff like ADD and autism didn’t come until much later. Parents just thought kids were being ridiculous and would beat the stupid out of them.

        Also, look at the number of vaccines given then versus now. Our kids are exposed to so much more now than they were back then.

        To comment on your polio comment, the best polio vaccine was the one with the live virus. That gave the best immunity. It also gave polio to the person getting vaccinated. So where’s that line? Risk getting it on your own, or risk getting complications from the chemicals in vaccines and still getting the disease itself?

  • Barn Cat

    There’s no evidence whatsoever to link vaccines to autism. It’s caused by defective sperm produced by older fathers having children.

    • Anonymous

      That is not true at all about defective sperm. Sperm is continually being made not the same as w/womens eggs. It is just a bunch of smoke and mirror propaganda to feed the sheep and lead them to the slaughter. There may be an immune system issue at best, but it could be overly sensitive or unactive. We may never know but the facts are these inoculations DO contribute to the condition of autism. I have 4 sons, all from the same father. My 2 older boys have autism. Both regressed after the MMR. Both boys have Hepatitis, but the strain is G&H,(BarnCat get this) this strain is not from nature but from their innoculations of HepB. The shot that was to help give them immunity, gave them this virus. (Wait it gets worse) they also have reads of anywhere from 400- 550 for the Titers of Measles. (Wait it gets worse) they contracted EVERY LIVE VIRUS that was injected to them but not Polio (why?) it was given in a suspended dormant form. With every shot they had an immediate fever, I was told to give Tylenol. Both boys experienced swelling of the brain (encephalitis) which is often misdiagnosed as an ear infection. My younger 2 boys have never been inoculated and are rarely sick. I can count on one hand how many times they have thrown up from being sick (both boys) and they are 8 and 9. The older 2 boys I lost count the first year of their lives. My husband was in his mid forties when we had the last two, so tell me Barn Cat all that you do not know. Do not speak what you do not know. One child, one family is one too many. This is not something anyone person would want to have to live with. It is devastating, exhausting and the evidence is undeniable. Read Deadly Immunity by Robert Kennedy Jr. and How to Raise a Healthy Child in spite of your Doctor. A great read. I wish you only good things.

  • Barn Cat

    http://www.forbes.com/sites/alicegwalton/2013/03/20/across-generations-older-grandfathers-may-transmit-autism-risk-to-their-grandkids/

    Last year, several studies came out showing that the age of the parents, and particularly the age of the father, seemed to increase a child’s risk for autism. Now, it seems that on top of the father’s age (or mother’s), it’s also the grandfather’s age at the time he conceived his child that can affect his grandchild’s risk of autism.

    A new study out today in JAMA Psychiatry looked at health records from over 5,900 Swedish people with autism, and 31,000 without, born after the year 1932. The researchers knew everyone’s psychiatric histories, the ages of the grandparents when they conceived a child, and the grandchild’s risk of autism. They analyzed the data to find correlations between these variables.

    Parental Age, Especially The Father’s, Is Linked To Genetic Mutations In The Child

    For men who had a daughter when they were 50 or older, their grandchild’s risk of autism was 79% higher, compared to grandfathers who’d had their daughters between 20 and 24. For men who had sons after age 50, their risk of having a grandchild with autism was 67% higher.

    • Eva

      I suggest you read this article, published in Rolling Stone 2009, about the use of mercury in vaccins and hidden proves that it CAUSES autism with American children on large scale and worse, is causing autism in third world countries as vaccins are dumped there. Imagine it were YOUR child.

      http://www.rollingstone.com/politics/news/deadly-immunity-20110209

    • Anonymous

      You are wrong and so is the study.