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  • Sebelius Asks Media to Censor Autism Debate

    By Katie Wright, noonehastodietomorrow.com
    03-17-2010 01:18

    “There are groups out there that insist that vaccines are responsible for a variety of problems, despite all scientific evidence to the contrary. We (the office of Secretary of Health and Human Services) have reached out to media outlets to try to get them not to give the views of these people equal weight in their reporting.”

    See Reader’s Digest HERE.

    That’s right. Kathleen Sebelius, the Secretary of HHS, has asked newspapers, magazines, television journalists, who knows who else- specifically NOT to listen to parents and scientists in the autism community, not to respect their concerns, not to take seriously the condition of chronically ill children with autism and to disregard a growing body of evidence questioning the safety of our infant and toddlers’ immunization schedule. If I have got anything wrong I would love to hear a tape or see a transcripts of these media “outreaches.”

    Pretty frightening stuff. Thank you to Jake Crosby who uncovered this frank and disturbing exchange between Arthur (autism is not so bad and there is no increase anyway) Allen and Ms. Sebelius.

    I am taking Ms. Sebelius at her word. Ms. Sebelius has unilaterally said that she knows that every single American parent who saw their child regress post vaccination or experience a severe adverse reaction is wrong and she knows better. Ms. Sebelius has ordered, suggested, beseeched, implored (?) American journalists NOT to “give these people (anyone concerned with vaccine safety) equal weight in their reporting” because she has decided by informal governmental decree that the debate is closed?

    Sounds like something that would happen in a communist dictatorship, right? Was there a similar decree when “citizen dissidents” questioned the safety of hormone replacement therapy for women? Was the media instructed to ignore those nuisances who were suspicious of a long denied link between hormone therapy and breast cancer? Did the HHS order a first amendment crackdown of those trouble-making women who had long complained that Fibromalgia was a real disease and not a psychosomatic condition. Menaces everywhere who dared to question medical authorities! They must be silenced! You have got to be kidding.

    Sebelius boasts that she holds an H1N1 meeting every single day but cannot find the time to attend one IACC meeting or meet with any autism organizations. Well, not exactly, apparently Ms. Sebelius is personal friends with Ms. Alison Singer, leader a vaccine marketing/ autism org financed in part by Dr. Paul Offit. Newsflash Ms. Seblius: 1 in 100 American children, and rising, have autism and this is a much bigger deal than H1N1. One in four American parents do not think vaccines are safe for their children. At least half of all families affected by autism believe too many vaccines too soon triggered their child’s autism. Hundreds of thousands of parents saw their child regress post multiple vaccinations. Sebelius’ answer to this massive crisis of confidence is media censorship?

    Hmmmm…..Censorship has a long and illustrious history- of not working. Thankfully, we live in a democracy with a free press. So I don’t know what is worse, the fact Sebelius asked that journalists censor the autism debate or the fact that they did.
    While I have not read more than a few reasoned, balanced or well written pieces of journalism on the subject of autism and vaccines I have read a host of spoon fed press releases masquerading as “news” stories about supposedly important autism research. Journalists from “Time”, “Newsweek”, “The New York Times”, online health resources etc. have reported in depth on such “breakthroughs” as a recent study concluding that “maternal sensitivity” is a good thing for autistic children, or Kennedy Krieger’s incredible finding that autistic kids have bad handwriting (amazing, I know!) or the Children’s Hospital of Boston study which found that cousins from the Middle East who marry are more likely to produce autistic kids. I know, stop the presses, a cure is within sight!

    In this embarrassing interview with Arthur Allen Ms. Sebelius asserts all the science is a closed book. At the top of the list of the science of vaccine safety studies are the definitive 2001 and 2003 “Pediatrics” articles. While the media has kept us front row center in the breaking developments regarding ASD kids with bad handwriting, journalists have neglected to report on perhaps one of the most striking recent events concerning the subject of autism research.

    An author of one of the most frequently cited “vaccines do not trigger autism” articles is Dr. Poul Thorsen. Well, well, well… this week we learned that Thorsen has allegedly absconded with approximately $2 million of CDC research money and is the target of an international police manhunt. We also learned that the Univ. of Aarhus, Denmark, where Thorsen was employed when conducting the studies (naturally in close cooperation w/ the CDC) has released a letter detailing Thorsen’s recently uncovered crimes. These crimes include but are not limited to: theft, forgery and assorted serious breaches of ethical norms.

    Apparently Thorsen was a very, very busy scientist. He was simultaneously and secretly employed at the Univ of Aarhus, Emory University, Drexel University and as a “visiting scientist at the CDC.” Emory and Drexel have, some might say, inappropriately close relationships with the CDC. There appears to be very little room for independent or unbiased science at these research centers. All three are heavily invested in denying any relationships between vaccines and autism. The CDC owns numerous vaccine patents and Emory and Drexel receive tremendous financial support from vaccine companies.

    Hmmmm…I know some of you might be thinking “Emory University is in the news a lot lately!” Yes, Emory has been in the news a great deal thanks to the amazing anti- corruption work of Senator Charles Grassley. Ms. Sebelius should dump Arthur Allen and have a conversation with someone who is actually doing something to restore public confidence in our health systems by fighting the fraud and greed inherent at places like Emory. Grassley is conducting an investigation a pervasive pattern of corruption among Emory researchers who fail to disclose significant financial conflicts of interest in the outcomes of the research they conduct. Isn’t it interesting that Thorsen found a second home there?

    Thorsen was working hard for everyone’s benefit: his own, his employers, pharmaceutical companies- everyone’s benefit, that is, except the public’s. The health and safety of American kids being administered the world’s most aggressive infant vaccine schedule was last on his list. Thorsen was also employed as a consultant on the official revisions of the all-important DMS V. Thorsen was advising how to count and classify autism cases. It is absolutely frightening that a wanted felon has such an enormous and pervasive influence on the lives of our children.

    So I am trying to get this straight Ms. Sebelius. Help me out here. We should take lying thieves with no interest in operating in the public’s interest at their word but the media should ignore parents and legitimate scientists who question the validity of vaccine science research performed by alleged criminals? I’m really confused!

    Wouldn’t it be great if Sebelius lifted her fatwa on vaccine research reporting and someone discovered what this creep Thorsen was actually up to at Drexel and Emory? Why was Thorsen a “visiting scientist at the CDC” at the same time? Apparently the CDC has known about this theft (of our money) for some time but has chosen to remain silent. I wonder why? How likely is it that Thorsen was the only scientist involved in what appears to be a massive and long term scheme to manipulate and forge scientific documents? Most importantly, why should the public believe that a thief and a liar with no ethical standards would be honest and scrupulous in his research? I shudder at the thought of Thorsen recounting “the facts” of his studies to students while asserting, as he frequently did, that “absolutely no more vaccine/autism research is warranted.” Now there’s a guarantee you can take to the bank. Oops, maybe a bank Thorsen hasn’t robbed.

  • New York State: All injectable versions of H1N1 vaccine will contain Thimerosal (mercury) preservative

    (FOX 40)   Because of the lack of the H1N1 vaccine available to people across the state, the New York Health Department has decided to change a state law so more people can get  vaccinated, quicker.

    Since 2008 the New York State Department of Health has not allowed  pregnant women and children under three to be given vaccines with Thimerosal in them.

    Thimerosal is a mercury containing preservative that keeps bacteria out of the vaccine.

    The ban was enacted so studies could be done on whether Thimerosal was linked to autism.

    No link has been found.

    Because the H1N1 vaccine can be made quicker with Thimersol in it, all injectable versions of the shot given out will contain Thimerosal.

    However, the department of health says close to 380,000 doses of the thimerosal-free vaccine is expected to be available in the state by late November.

    See also: How mercury causes brain neuron degeneration- U of Calgary

  • How Mercury Causes Brain Neuron Degeneration – University of Calgary

  • Study Proves Link Between Thimerosal and Autism Neurotoxicity

    Natural News
    Tuesday, September 01, 2009 by: Aaron Turpen, citizen journalist

    Key concepts: Thimerosal, Autism and Mercury
    View on NaturalPedia: Thimerosal, Autism and Mercury

    (NaturalNews) In a study just published, a causal connection between Thimerosal, the preservative often used in vaccines, and the brain pathology found in patients diagnosed with autism spectrum disorder (ASD), has been established. The study, A Mitochondrial Dysfunction, Impaired Oxidative-Reduction Activity, Degeneration, and Death in Human Neuronal and Fetal Cells Induced by Low-Level Exposure to Thimerosal and Other Metal Compounds was published in the June 2009 issue of the peer-reviewed journal Toxicology & Environmental Toxicology.1

    In the study, it was found that the amounts of Thimerosal found in inoculations commonly given to infants in the 1990s and still in use today (though more limited) induced levels of cellular toxicity. This cellular damage was consistent with that found in studies of patients diagnosed with ASD.

    Both studies found significant mitochondrial dysfunction, reduced cellular oxidative-reduction activity, cell degeneration, and cell death being tied to ASD. All of these contribute significantly to ASD diagnosis and are also often attributed to other childhood and early development maladies.

    Here at Natural News, of course, readers are likely well aware of the links between Thimerosal and autism. Until now, those links have mostly been implied and inferred through anecdotal evidence and court cases. Nevertheless, the link between mercury, Thimerosal and childhood autism rates has been exhaustively covered here.2

    Now, conclusive scientific evidence that cannot be ignored has been published in a peer-reviewed journal. This gives those of us concerned with the issue more ammunition to use in forcing lawmakers to acknowledge the link and for pharmaceutical companies who’ve been pushing their wares on us to become accountable for it.

    This study also showed that Thimerosal is much more toxic than other metal compounds included in the study and commonly found in vaccines. Other compounds studied included aluminum sulfate, methylmercury hydroxide (often blamed for autism), lead acetate, and mercuric chloride. This study does not take those compounds off the hook, of course, but does show that Thimerosal is significantly more toxic than even methylmercury.

    The explanation for that higher toxicity lies in the fact that Thimerosal is not naturally-based, but manufactured.

    First created in the 1920s as a stronger replacement for alkylmercury compound, it’s biological transport and intracellular delivery properties were enhanced. The study shows that, in comparison to methylmercury hydroxide, Thimerosal has three distinct toxicity-enhancers:

    1. Higher aqueous solubility – the ability to dissolve in water.
    2. Higher solubility in cell membranes – the ability to dissolve in cell membranes.
    3. Higher intracellular toxicity – the ability to inactivate essential cell processes.

    The study was done by CoMeD, Inc. (a non-profit) through a grant from the Brenen Hornstein Autism Research & Education Foundation and the non-profit Institute of Chronic Illnesses, Inc. Attribution was also given to the Genetic Centers of America.

    CoMeD, Inc. and BHARE recommend parents and health care providers have children with ASD diagnosis tested by urinary porphyrin profile analysis (UPPA). More information is available at CoMeD’s website Mercury-freeDrugs.org, including free information on ordering UPPA tests as well as papers validating those tests.

    Resources:
    1 – A Mitochondrial Dysfunction, Impaired Oxidative-Reduction Activity, Degeneration, and Death in Human Neuronal and Fetal Cells Induced by Low-Level Exposure to Thimerosal and Other Metal Compounds http://www.informaworld.com/smpp/co…

    2 – Natural News “Thimerosal” articles: http://www.naturalnews.com/GoogleSe…

    3 – Press Release from CoMeD on study: http://mercury-freedrugs.org/docs/0…

    Abstract of the study:

    Mitochondrial dysfunction, impaired oxidative-reduction activity, degeneration, and death in human neuronal and fetal cells induced by low-level exposure to thimerosal and other metal compounds

    Authors: D. A. Geier a;  P. G. King b; M. R. Geier c
    Affiliations: a Institute of Chronic Illnesses, Inc., Maryland, USA
    b CoMeD, Inc., Maryland, USA
    c The Genetic Centers of America, Maryland, USA
    DOI: 10.1080/02772240802246458
    Publication Frequency: 8 issues per year

    Published in: journal Toxicological & Environmental Chemistry, Volume 91, Issue 4 June 2009 , pages 735 – 749

    First Published: June 2009

    Formats available: HTML (English) : PDF (English)
    Previously published as: Toxicological & Environmental Chemistry Reviews (0092-9867) until 1980
    Article Requests: Order Reprints : Request Permissions

    Abstract

    Thimerosal (ethylmercurithiosalicylic acid), an ethylmercury (EtHg)-releasing compound (49.55% mercury (Hg)), was used in a range of medical products for more than 70 years. Of particular recent concern, routine administering of Thimerosal-containing biologics/childhood vaccines have become significant sources of Hg exposure for some fetuses/infants. This study was undertaken to investigate cellular damage among in vitro human neuronal (SH-SY-5Y neuroblastoma and 1321N1 astrocytoma) and fetal (nontransformed) model systems using cell vitality assays and microscope-based digital image capture techniques to assess potential damage induced by Thimerosal and other metal compounds (aluminum (Al) sulfate, lead (Pb)(II) acetate, methylmercury (MeHg) hydroxide, and mercury (Hg)(II) chloride) where the cation was reported to exert adverse effects on developing cells. Thimerosal-associated cellular damage was also evaluated for similarity to pathophysiological findings observed in patients diagnosed with autistic disorders (ADs). Thimerosal-induced cellular damage as evidenced by concentration- and time-dependent mitochondrial damage, reduced oxidative-reduction activity, cellular degeneration, and cell death in the in vitro human neuronal and fetal model systems studied. Thimerosal at low nanomolar (nM) concentrations induced significant cellular toxicity in human neuronal and fetal cells. Thimerosal-induced cytoxicity is similar to that observed in AD pathophysiologic studies. Thimerosal was found to be significantly more toxic than the other metal compounds examined. Future studies need to be conducted to evaluate additional mechanisms underlying Thimerosal-induced cellular damage and assess potential co-exposures to other compounds that may increase or decrease Thimerosal-mediated toxicity.
    Keywords: autism; glial; lead; mercury; mercuric; neurodevelopmental