Chronic illnesses are coming as a result. I have been warning for years against this. Here’s a recent YouTube video. Before you potentially harm your child, do the research that your MD’s don’t bother reading about:
Archive for the ‘Vaccines and Autism’ Category
For years the USA has lead the nations of the world in being first and foremost with cases of “modern man illnesses” such as Alzheimer’s disease, Acrodynia, Parkinson’s Disease, Multiple Sclerosis, ALS, and now Autism. The rate of Autism has reached incredible levels recently in the USA and yet seems not to be given the attention such a disaster deserves.
• The USA is remarkable in that we now have the highest rate and number of vaccines given the earliest to infants and now have one of the highest rates of infant mortality in the Western nations as well as the highest rate of autism by far.
• In spite of our high level of science and technology in biomedicine we still claim that all of the illnesses given above have “no known cause”——but common sense and a basic understanding of biological science tells us the causes cannot be purely genetic and that a toxic exposure is required, and it is scientifically logical the mercury compounds in our vaccines are the primary cause for early infant death and autism.
• Due to the involvement of the CDC in the vaccine program it is critical that an unbiased group be formed to look at the both the toxic effects of our vaccines and other questions concerning the efficacy of the CDC vaccine program (remember the mumps epidemic where about 85% of those infected were also vaccinated?). The CDC administrators cannot play a controlling role in this evaluation of the vaccine program.
• The autism epidemic started soon after the CDC mandated vaccine program was implemented and it is a good question to ask our health authorities “if the CDC vaccine program prevents significant amounts of infant death from infectious diseases then what are USA infants dying of that place the USA at such a disastrous position in comparison to other progressive countries?”
• It is critical to have an independent research group do an epidemiological study of the rate of autism of non-vaccinated children versus vaccinated children. The CDC has refused to do this and has instead employed foreign researchers to do studies on foreign data bases where the exposure to mercury from vaccines was much later and much lower and where the autism rate was also commensurately lower. This scientifically illogical stand by CDC administrators has greatly damaged the entire reputation of the CDC, especially since two of the foreign epidemiologists who were involved and paid by the CDC are now facing criminal charges.
• Note that autism and other autism spectrum disorders affect boys much more than girls—and it is documented science that mercury and organic mercury compounds are more toxic to the male species. Most toxins show little gender difference.
• I could go on much longer but brevity may be best to focus on the issue that the USA health agencies are more and more losing the faith of the American people and seem unable to solve the problems leading to the causation and prevention of the “modern man illnesses”. This failure is most likely because modern medicine does not want to consider that these illnesses are primarily caused by toxic exposures generated by pharmaceutical based toxins delivered by physicians and dentists. It is the failure of modern medicine to comprehend the toxicity of low level exposures to heavy metals that leads to damaging of our most susceptible citizens, our infants and elderly.
Boyd E. Haley, PhD
Professor Emeritus
University of Kentucky
Chemistry Department
2430 Palumbo Drive, Suite 140
Lexington, KY 40509-1117
The lead author of a key study used by EU and USA health bodies as evidence mercury in vaccines does not cause autism has vanished after it emerged that he fraudulently claimed 10 million crowns ($1.8m) in funds from Aarhaus University in Denmark.
FROM DR. TEN PENNY = Dr. Wakefield has never been “anti-vaccine.” His work has always been focused on finding an explanation for WHY so many autistic children have terrible bowel disease.
Dr. Wakefield has always recommended single antigen vaccines. He hypothesized that the three live viruses given together in the MMR vaccine are the source of potential problems in at least SOME children.
Learn more: http://www.cent4dent.com/html/mercury_issues/vaccines.html
Read the whole article: http://drtenpenny.com/Wakefield_Inquisitioners_Have_their_day.aspx
ScienceDaily (Jan. 11, 2010) — Studying a rare disorder known as tuberous sclerosis complex (TSC), researchers at Children’s Hospital Boston add to a growing body of evidence suggesting that autism spectrum disorders, which affect 25 to 50 percent of TSC patients, result from a miswiring of connections in the developing brain, leading to improper information flow. The finding may also help explain why many people with TSC have seizures and intellectual disabilities.
Findings were published online in Nature Neuroscience on January 10.
TSC causes benign tumors throughout the body, including the brain. But patients with TSC may have autism, epilepsy or intellectual disabilities even in the absence of these growths. Now, researchers led by Mustafa Sahin, MD, PhD, of Children’s Department of Neurology, provide evidence that mutations in one of the TSC’s causative genes, known as TSC2, prevent growing nerve fibers (axons) from finding their proper destinations in the developing brain.
Studying a well-characterized axon route — between the eye’s retina and the visual area of the brain — Sahin and colleagues showed that when mouse neurons were deficient in TSC2, their axons failed to land in the right places. Further investigation showed that the axons’ tips, known as “growth cones,” did not respond to navigation cues from a group of molecules called ephrins. “Normally ephrins cause growth cones to collapse in neurons, but in tuberous sclerosis the axons don’t heed these repulsive cues, so keep growing,” says Sahin, the study’s senior investigator.
Additional experiments indicated that the loss of responsiveness to ephrin signals resulted from activation of a molecular pathway called mTOR, whose activity increased when neurons were deficient in TSC2. Axon tracing in the mice showed that many axons originating in the retina were not mapping to the expected part of the brain.
Although the study looked only at retinal connections to the brain, the researchers believe their findings may have general relevance for the organization of the developing brain. Scientists speculate that in autism, wiring may be abnormal in the areas of the brain involved in social cognition.
“People have started to look at autism as a developmental disconnection syndrome — there are either too many connections or too few connections between different parts of the brain,” says Sahin. “In the mouse models, we’re seeing an exuberance of connections, consistent with the idea that autism may involve a sensory overload, and/or a lack of filtering of information.”
Sahin hopes that the brain’s miswiring can be corrected by drugs targeting the molecular pathways that cause it. The mTOR pathway is emerging as central to various kinds of axon abnormalities, and drugs inhibiting mTOR has already been approved by the FDA. For example, one mTOR inhibitor, rapamycin, is currently used mainly to prevent organ rejection in transplant patients, and Sahin plans to launch a clinical trial of a rapamycin-like drug in approximately 50 patients with TSC later this year, to see if the drug improves neurocognition, autism and seizures.
In 2008, Sahin and colleagues published related research in Genes & Development showing that when TSC1 and TSC2 are inactivated, brain cells grow more than one axon — an abnormal configuration that exacerbates abnormal brain connectivity. The mTOR pathway was, again, shown to be involved, and when it was inhibited with rapamycin, neurons grew normally, sprouting just one axon.
Supporting the mouse data, a study by Sahin and his colleague Simon Warfield, PhD, in the Computational Radiology Laboratory at Children’s, examined the brains of 10 patients with TSC, 7 of whom also had autism or developmental delay, and 6 unaffected controls. Using an advanced kind of MRI imaging called diffusion tensor imaging, they documented disorganized and structurally abnormal tracts of axons in the TSC group, particularly in the visual and social cognition areas of the brain (see image). The axons also were poorly myelinated — their fatty coating, which helps axons conduct electrical signals, was compromised. (In other studies, done in collaboration with David Kwiatkowski at Brigham and Women’s Hospital, giving rapamycin normalized myelination in mice.)
Sahin has also been studying additional genes previously found to be deleted or duplicated in patients with autism, and finding that deletion of some of them causes neurons to produce multiple axons — an abnormality that, again, appears to be reversed with rapamycin.
“Many of the genes implicated in autism may possibly converge on a few common pathways controlling the wiring of nerve cells,” says Sahin. “Rare genetic disorders like TSC are providing us with vital clues about brain mechanisms leading to autism spectrum disorders. Understanding the neurobiology of these disorders is likely to lead to new treatment options not only for TSC patients, but also for patients with other neurodevelopmental diseases caused by defective myelination and connectivity, such as autism, epilepsy and intellectual disability.”
The current study was funded by grants from the National Institutes of Health, the John Merck Scholars Fund, Tuberous Sclerosis Alliance, the Manton Foundation, the Children’s Hospital Boston Translational Research Program, and the Children’s Hospital Boston Mental Retardation and Developmental Disabilities Research Center.
Duyu Nie was first author on the paper. Coauthors were Duyu Nie, Alessia Di Nardo, Juliette M Han, Hasani Baharanyi, Ioannis Kramvis, and ThanhThao Huynh, all of the F.M. Kirby Neurobiology Center and Department of Neurology, Children’s Hospital Boston; Sandra Dabora of Brigham and Women’s Hospital; Simone Codeluppi and Elena B Pasquale of the Burnham Institute for Medical Research, and University of California San Diego; and Pier Paolo Pandolfi of Beth Israel Deaconess Cancer Center.
For more info, look at the Mercury and Autism pages of My Website.
Please note, further conversations about H1N1 vaccination and swine flu are under their own subject heading now.
The government has overstated the efficacy. read more
Visit our website: www.cent4dent.com for more information about the links between vaccination and autism.
Delayed Acquisition of Neonatal Reflexes in newborn Primates receiving A Thimerosal-containing HepatitiS B Vaccine: influence of gestational age and Birth weight
Abstract
This study examined whether acquisition of neonatal reflexes and sensorimotor skills in newborn rhesus macaques (Macaca mulatta) is influenced by receipt of the single neonatal dose of Hepatitis B (HB) vaccine containing the preservative thimerosal (Th). HB vaccine containing a standardized weight-adjusted Th dose was administered to male macaques within 24 hours of birth (n = 13). Unexposed animals received saline placebo (n = 4) or no injection (n = 3). Infants were raised identically and tested daily for acquisition of 9 survival, motor, and sensorimotor reflexes by a blinded observer. In exposed animals there was a significant delay in the acquisition of three survival reflexes: root, snout and suck, compared with unexposed animals. No neonatal responses were significantly delayed in unexposed animals compared with exposed. Gestational age (GA) and birth weight were not significantly correlated. Cox regression models were used to evaluate the main effects and interactions of exposure with birth weight and GA as independent predictors and time-invariant covariates. Significant main effects remained for exposure on root and suck when controlling for GA and birth weight such that exposed animals were relatively delayed in time-to-criterion. There was a significant effect of GA on visual follow far when controlling for exposure such that increasing GA was associated with shorter time-to-criterion. Interaction models indicated that while there were no main effects of GA or birth weight on root, suck or snout reflexes there were various interactions between exposure, GA, and birth weight such that inclusion of the relevant interaction terms significantly improved model fit. This, in turn, indicated important influences of birth weight and/or GA on the effect of exposure which, in general, operated in a way that lower birth weight and/or lower GA exacerbated the detrimental effect of vaccine exposure. This primate model provides a possible means of assessing adverse neurodevelopmental outcomes from neonatal Th-containing HB vaccine exposure, particularly in infants of lower GA or low birth weight. The mechanism of these effects and the requirements for Th is not known and requires further study.
This information presented for educational purposes by The Centre for Dentistry at Haddon, Haddon Heights, NJ. For further information about vaccines and autism please .
Laura Hewitsona, c, , , Lisa A. Housera, Carol Stottc, Gene Sackettb, Jaime L. Tomkoa, David Atwoodd, Lisa Blued, E. Railey Whited and Andrew J. Wakefieldc
a Department of Obstetrics and Gynecology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213
b Washington National Primate Research Center, University of Washington, Seattle, WA 98195
cThoughtful House Center for Children, Austin, TX, 78746
dDepartment of Chemistry, University of Kentucky, Lexington, KY 40506
A new study in the leading scientific journal NeuroToxicology lends further credence to parents and scientists concerned about an increasingly aggressive childhood vaccine schedule and toxic vaccine components. A team led by researchers at the University of Pittsburgh found that infant macaque monkeys receiving a single Hepatitis B vaccine containing the mercury-based preservative thimerosal underwent significant delays in developing critical reflexes controlled by the brainstem. The infant macaques that did not receive vaccines developed normally.
Government vaccine guidelines were expanded in 1991 to include a Hepatitis B vaccine for infants within the first few days of life, even though the disease is primarily transmitted sexually or spread through the use of dirty needles. [Markus' Note: Dr. Sherry Tenpenny has stated that allowing your child to be innoculated at birth is just like saying, "Yep, better get it done now, because by the time my child is 10 he or she will be an IV-drug-using child prostitute.]The introduction of the shot was part of a greatly accelerated vaccine schedule that coincides with the drastic increase in autism, which now affects one in 100 American children. Thimerosal was removed from U.S. Hepatitis B vaccines in 2000 but was not recalled from the market and was administered for approximately two more years. It still remains in other vaccines including all multi-dose shots for both the seasonal flu and H1N1.
Current government recommendations for seasonal flu and H1N1 call for pregnant women to receive both vaccines, and children as young as six months to receive as many as four separate flu shots. “This also doesn’t take into account that nursing infants may be exposed to additional mercury through breastmilk should both mother and baby be vaccinated,” says National Autism Association (NAA) board chair Lori McIlwain. “This study’s outcome confirms that such an over-the-top toxic vaccine schedule is an assault on the developing brains of our children.”Specifically, the study found:
– Thirteen newborn rhesus macaques were given a Hepatitis B vaccine containing a standardized dose of thimerosal adjusted for their weight, four received a saline placebo, and three were not given any shots.
– Vaccinated animals experienced a significant delay in the acquisition of three survival reflexes compared to unvaccinated animals. Root, snout, and suck reflexes, critical to animal survival in the wild, were delayed in the vaccinated macaques.
– These reflexes are controlled by the brainstem, a vital part of the brain that regulates automatic functions such as breathing, heart rate, and intestinal activity.v — Neonatal responses in unvaccinated control animals were not delayed.
– The delay in acquisition of three of the four survival reflexes was not contingent on birth weight or gestational age.
For years, parents of children with autism have lobbied government health agencies to conduct research comparing the health of vaccinated children to that of unvaccinated children, and to remove thimerosal from all vaccines. Neither request has been met.
“This study underscores the lack of appropriate government action to ensure the safety of vaccines. Had our government agencies conducted the most basic research on the implications to children’s health from the vaccines they rigorously promote, they could have spared thousands of children the neurological injuries they endure today,” said Ms. McIlwain. “It’s shameful.”
This information presented for educational purposes by The Centre for Dentistry at Haddon, Haddon Heights, NJ. For further information about vaccines and autism please
This is taken from Dr. Mercola’s article, today. There are NINE IMPORTANT REASONS NOT TO LET YOUR PEDIATRICIAN TALK YOU INTO VACCINATION! In my eyes, this is the most important:
“3.Adjuvants are added to vaccines to boost production of antibodies but may trigger autoimmune reactions. Some adjuvants are mercury (thimerosal), aluminum and squalene. Why would you sign a consent form for your children to be injected with mercury, which is even more brain-toxic than lead?”
To read them all, click here.
For more information about Vaccinations and Autism, click here.
An additional article, published today indicates that the incidence of Autism is much higher than the 1 in 150 that was reported just two years ago. It is more like one in a hundred. Protect your children.
This message brought to you for educational purposes only.