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Neonatal Administration of Thimerosal Causes Persistent Changes in Mu Opioid Receptors in the Rat Brain.Department of Pharmacology and Physiology of the Nervous System, Institute of Psychiatry and Neurology, Sobieskiego 9 str., 02-957, Warsaw, Poland. AbstractThimerosal added to some pediatric vaccines is suspected in pathogenesis of several neurodevelopmental disorders. Our previous study showed that thimerosal administered to suckling rats causes persistent, endogenous opioid-mediated hypoalgesia. Here we examined, using immunohistochemical staining technique, the density of mu-opioid receptors (MORs) in the brains of rats, which in the second postnatal week received four i.m. injections of thimerosal at doses 12, 240, 1,440 or 3,000 mug Hg/kg. The periaqueductal gray, caudate putamen and hippocampus were examined. Thimerosal administration caused dose-dependent statistically significant increase in MOR densities in the periaqueductal gray and caudate putamen, but decrease in the dentate gyrus, where it was accompanied by the presence of degenerating neurons and loss of synaptic vesicle marker (synaptophysin). 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.
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This process of the public recognizing and accepting that autism is preventable and treatable is moving much more slowly than it should have (It should have made the front page of the NYT just after the turn of the century and that should have been it), but it is moving, the paradigm has shifted, and things are not going back to the way they were. Try as they might, the hypervaccinators, Pharma shills and government ass coverers have not been able to keep the public, and growing sections of the medical community, from understanding that the autism epidemic is indeed an epidemic and is the result of the toxic avalanche coming down on our little ones from before conception until they get their last, brain inflaming doses of untested and under-tested vaccines. This month we saw the Senate finally hear that autism is an environmental illness, in which mercury is implicated (despite the best spinning that the best PR spinners have tried). This year we saw the country walk away from THE biggest scare campaign to dose the country with mercury toxic vaccines in my lifetime. People get that vaccines are a serious risk and are taking action to mitigate that risk. This news piece is just another example of the fact that mainstream medicine and media gets it, and while they cant' yet say the V word, using the mercury word is surely code for vaccines, so they might as well. In my mind, the announcement of the Poling concession was D day, and we are now in the march across Europe. But this war will end as people come to see what Pharma and Govt have done, and how they have lied to the public, and as they retire, those who come in behind them, who do not have blood on their hands and can admit that things have gone way over the line, will pull back. We will likely never get our apology, but as we see in this story, and in the Senate last month, they know. And they are making changes. If the autism story ends like the thalidomide story, I will die a happy woman.
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So this is happening: Greeters and Admins needed for Mobile flu Clinic posted: August 19, 2010, 03:05 PM
PUSH MODELS!!!!
Promotional Modeling Agency looking to hire Brand Ambassadors for an upcoming 6 week program. We are staffing a Mobile Flu Clinic that will be in Bangor Mall in Bangor, ME. We need outgoing, attractive, enthusiastic, and intelligent guys or girls between the ages of 18-30.
This is also a great opportunity for advancement in doing more promotional work. This program will run for 6 consecutive weekends (Saturdays and Sundays only). We are booking ambassadors for all 6 weekends, or every other weekend.
Please apply online at www.pushmodels.com. After you have filled out your profile, please email Amber Gordon at ag@pushmodels.com, put "Mobile Flu Clinic" in subject line, and specify that you will work in Bangor, ME. Salary/Wage: $12/hr Shift: Weekends
• Location: Bangor Hot chicks that sell beer and cars... now used to sell vaccines.
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Wow what a great day we had yesterday! Nanci Grenier Boutet owns the Aquaholics Surf Shop in Kennebunk, Maine and has a heart for our kids. So three times in the Summer, the first Tuesday of June, July and August, she gives a big shout out to all the local surfers to come to Kennebunk Beach and take our special little ones surfing. We went yesterday for the first time, Chandler surfed until he was a Popsicle, and loved every minute of it. Tommy, Chandler's cutie pie surfing coach, comes down from his home in Quebec to vacation in Maine with his family in August, and he takes part in the event while they are here. Chan had a great time with Tommy and learned how to say, "Merci, Tommy" at the end of the day. Here are the best shots from yesterday. It was so wonderful to see all our little guys loving the time they were having in the water, their dad's being able to do real father son sports bonding stuff that happens so rarely with our kids and, of course, to have a nice zone of love around our kids where they could be their wierd, loud, difficult, haphazard selves with out a judgmental look or nasty comment as far as they eye could see. Thanks so much to Nanci for doing this and thanks so much to all the loving, supporting, understanding surfers who made our kids day! All my pictures from the day will be posted here, and anyone connected with the event has my permission to download and use them in any way they like (as long as it is respectful to those in the images, of course). If anyone connected with the event would like hi res images, contact me at mail@adventuresinautism.comThese are the best pics of the day. Fog rolled in at the end, so those are not as clear, but as you can see... a good time was had by all.    | | My Webster |
 | | Chandler having a ball in his wet suit |
    | | Sensory issues in full effect, but didn't end up standing in anyone's way |
  | | For this little guy, getting his wet suit on was the hardest part, but dad got him through it. |
 | | Nick meets his teacher, Josh Wilbur |
 | | The instruction begins |
 | | Susan preps Scotty for the water |
     | | Loucas learning how to pup up |
 | | Some took things slow and easy |
 | | Some were a little bolder |
   | | But they were all loving it |
 | | Don't miss the guy in the back |
 | | Nanci introduces Chandler to Thomas Duplessis who taught him. Chan was so eager to get in the water that daddy never got the chance to change into his swim suit. |
   | | Happy guy |
   | | Chan's first big ride |
 | | Loucas and Chandler decide they are ready for the big waves |
    | | Loucas totally rocks on the surfboard |
  | | This guy was great. He got up several times and clearly is on his way to really surfing |
   | | Picture of the day! Don't know who is happier, Stephen for surfing so well, or his friend when he sees Stephen! |
 | | This little girl was so precious. Every time I saw her, just huge grins while being out on the water. It was infectious. |
    | | As the fog was rolling in, I ran down to the end of the beach to catch these two. Biggest shredders of the day. |
  | | I think that this might be my favorite. This guy, God bless him, is working his butt off to make this kid happy, and his joyful face is the big pay off. |
  | | Thank you for being there for our kids. |
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Came across this today: BBB Wise Giving Report for Autism Speaks
BBB Wise Giving Report issued September 2009 BBB Wise Giving Report expires September 2011
Does not meet one or more standards This charity does not meet one or more of the 20 standards for Charity Accountability. http://www.facebook.com/group.php?gid=109130859120272
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Wonder if it skews Reuters coverage of let's say... MMR or Gardasil or RotaTeq or.... Thomas H. Glocer
Chief executive officer, Thomson Reuters Corporation (information and services company for businesses and professionals). Director, Thomson Reuters Corporation, Partnership for New York City. New Merck director since November 3, 2009 No mention here that the CEO of the news agency reporting had a very vested interest in seeing MMR exonerated, now is there. And Dr. Wakefield said the charges were unjust... did they look into his claim? British ban for doctor at heart of MMR vaccine row
By Kate Kelland, Health and Science Correspondent
LONDON | Mon May 24, 2010 12:44pm BST
LONDON (Reuters) - A doctor whose claims of links between vaccination and autism triggered a scientific storm before being widely discredited was struck off the medical register Monday for professional misconduct.
Dr Andrew Wakefield's 1998 study led many parents to refuse to have their children vaccinated with the measles, mumps and rubella (MMR) shot and has been blamed for a big rise in measles cases in the United States and parts of Europe in recent years.
A disciplinary panel of the General Medical Council (GMC) found that Wakefield had acted in a "dishonest," "misleading" and "irresponsible" way during his research.
The ruling means Wakefield, who now lives and works in the United States, can no longer practise as a doctor in Britain, but can continue to work in medicine outside the UK.
His paper, published in The Lancet medical journal but since widely discredited, caused one of the biggest medical rows in a generation.
"The panel has determined that Dr Wakefield's name should be erased from the medical register," the GMC said in a statement.
Wakefield had failed to disclose various details about the funding of the study -- a failure the GMC described as "dishonest and misleading" -- and had acted "contrary to the clinical interests" of the children involved in his research.
Striking Wakefield off the medical register was "the only sanction that is appropriate to protect patients" and was in the wider public interest. It was also "proportionate to the serious and wide-ranging findings made against him," the statement said.
Data released last February for England and Wales showed a rise in measles cases of more than 70 percent in 2008 from the previous year, mostly due to a fall in the number of children being vaccinated. Vaccination rates are now recovering.
Terence Stephenson, president of the Royal College of Paediatrics and Child Health, said the false suggestion of a link between autism and the MMR vaccine had caused "untold damage" to vaccination programs.
"We cannot stress too strongly that all children and young people should have the MMR vaccine. Overwhelming scientific evidence shows that it is safe," he said in a statement.
Wakefield defended his work, and said the GMC had sought to deny that the case against him was related to whether the vaccine was safe, and specifically, whether it caused autism.
"Efforts to discredit and silence me through the GMC process have provided a screen to shield the government from exposure on the ... MMR vaccine scandal," he said in a statement.
The GMC said his refusal to accept that he had made mistakes meant that a temporary suspension of Wakefield's licence was not enough and he should be banned altogether.
"Dr Wakefield's continued lack of insight as to his misconduct serve only to satisfy the panel that suspension is not sufficient and that his actions are incompatible with his continued registration as a medical practitioner," it said.
(Editing by Andrew Roche)
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cid:_1_0E51C98C0E51C4D00074D2AC8825777D OFFICE OF PUBLIC AFFAIRS 1250 BELLFLOWER BLVD. * LONG BEACH, CALIFORNIA 90840-0116 * 562/985-4134 FAX 562/985-8109
PRESS RELEASE
FOR IMMEDIATE RELEASE August 12, 2010 F2010-024
Cal State Long Beach Biochemist's Research Supports Premise That Chemical Plasticizers May Contribute to Autism and Alzheimer's Disease
Who knew that brine shrimp—the tiny creatures popularly known as “Sea-Monkeys”—could reveal problems with chemicals found in plastics or even contribute to potential treatments for neurological conditions such as Alzheimer’s disease and autism?
Roger Acey, a professor of biochemistry at California State University, Long Beach (CSULB), and students in his lab have been studying the biology and genetics of embryonic development, using brine shrimp, Artemia salina, as a biological model. He is particularly interested in how environmental contaminants affect development.
“I think all baby boomers understand Sea-Monkeys,” Acey explained. “As kids, you could order them from suppliers advertising in comic books and grow them at home.” Artemia have long been used in scientific research and remain popular in science education at school and home. The shrimp grow up to three-quarters of an inch long and can live for some time once hatched.
Acey’s lab initially looked at how exposing the shrimp to toxic metals like copper, mercury, cadmium, etc., could affect their development. While continuing this successful work, which led to discovery of a shrimp protein that can capture metals, Acey took his ongoing research with Artemia in another direction.
“We began looking at plasticizers and how they might affect embryonic development,” he said. “We started looking at phthalate esters—compounds that give plastic bottles their malleability. They’re found in PVC (polyvinyl chloride), blood bags, plastic tubing, cosmetics and children’s toys, and are well known environmental contaminants. They have been reported to be teratogens (causing birth defects), carcinogens and endocrine disruptors. Endocrine disruptors are compounds that resemble the structure of estrogens and mimic the activity of these hormones. There are examples of populations of fish that are essentially all female due to phthalate ester contamination. Most recently, phthalate esters have been implicated in Type II diabetes.
“We made a series of phthalate esters (phthalates) with increasing the carbon chain lengths and started looking at the effect of these compounds on developing shrimp,” he continued. “Diethyl and dimethyl are non-toxic; di-n-propyl was slightly toxic; but di-n-butyl (DBP), which is the most commonly found phthalate, turns out to be the most toxic.”
As the shrimp develop, they produce an enzyme that metabolizes the DBP, he said. “At first, we called the enzyme DBPase. As soon as the shrimp hatch and begin to develop, DPBase activity increases dramatically. If you expose the shrimp to phthalate during the early period of development, they died. If you expose the shrimp to the phthalate later in development, the compound is no longer toxic. The idea is that there is a well-defined period of development when the embryos are sensitive to the phthalate. Therefore, we began looking for a specific biochemical event that was impacted by the DBP.” He has since identified DBPase as butyrylcholinesterase.
He noted that the shrimp were being affected by DBP at the point where their nervous system was beginning to develop, adding that shrimp have a cholinergic nervous system similar to humans in that they both use a chemical neurotransmitter called acetylcholine.
He and his students have since used umbilical cord stem cells to study the role of butyrylcholinesterase in developing neurons and the effect of DBP. “After the stem cells are activated and begin to develop into a neuron, the DBP becomes toxic. We think what is happening is that the DBP prevents the butyrylcholinesterase from performing its normal biological function. We’re currently in the process of determining the exact function of the enzyme," Acey said.
Acey is interested in how plasticizers might be connected to the dramatic rise in autism and Alzheimer’s disease. A recent study has shown that rat fetuses exposed to DBP develop symptoms characteristic of autism. "If you think about it, this suggests compounds that interact with butyrylcholinesterase could induce neurological problems,” he said.
That led him to consider another plasticizer, bisphenol A, commonly called BPA, which is being widely studied for its possible toxicity. Acey’s group has shown that BPA is an inhibitor of butyrylcholinesterase. “Again, the concern is that since this compound interacts with butyrylcholinesterase, it may have a pronounced effect on neuron development,” he said. Acey believes every effort should be made to prevent exposure of pregnant women and infants to these types of compounds.
“Interestingly, the level of brain butyrylcholinesterase is significantly increased in Alzheimer’s patients,” he said. Current therapeutics used in the treatment of Alzheimer’s disease target butyrylcholinesterase, so he and CSULB Professor Ken Nakayama are collaborating on further examining the biochemistry of this enzyme and its possible connections to Alzheimer’s disease.
“Dr. Nakayama, an organic chemist, had a series of compounds he wanted tested on an enzyme from bacteria,” Acey said. “I suggested we test his compounds on butyrylcholinesterase. The results of the experiments revealed that the compounds are potent inhibitors of butyrylcholinesterase and, as such, are potential therapeutics for the treatment of Alzheimer’s disease. Alzheimer’s patients lose their cognitive functions as a result of the decrease in the level of a specific neurotransmitter. Compounds that inhibit butyrylcholinesterase result in an increase in the level of neurotransmitters —the compounds responsible for memory— and the patients begin to recover their memory.”
They’ve applied for a patent for the compounds and are preparing to write a grant proposal to fund further studies to demonstrate whether the compounds can cross the blood-brain barrier. Acey remarked that some autistic children are responding to certain Alzheimer’s drugs, so the hope is that these compounds might someday be the basis for new medications to treat both conditions.
Acey’s research has been funded by grants from CSULB, the March of Dimes, the National Institutes of Health, and the California State University Program for Education and Research in Biotechnology (CSUPERB).
To learn more about Acey’s research, visit http://chemistry.csulb.edu/roger-acey.html.
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This week I started another blog. Lives Lost to Autism. It has stirred up some discussion, so I thought I would address it here. Five years ago I got into a discussion with some in the autism community on the neurodiversity side of things on whether or not it was wrong to try to 'cure' children with autism if it changed their personality. I argued that a) if getting poisons/bacteria/viruses out and getting nutrients/oxygen in, making the individual more healthy, changes some personality traits, then those traits were not a part of the real personality anyway, b) that improving health CANNOT make them into someone that they are not and c) even if it did fundamentally change someone's personality, it was worth it in the end because autism is a threat to the individual who has it, and even to some of the people that surround them. To illustrate my point, I planned to spend two months posting the stories where someone with autism was put in danger or killed as a result of their autism, stories that I had avoided like the plague because they truly crippled me with misery (my boy is a runner). I didn't last two months, but there were enough stories to illustrate my point in a few weeks, with members of the ND community even calling many to my attention things that I had not seen, so I cut it short int order to avoid the pain of the stories themselves. The series can be found here: Autism is DangerousThe discussion was primarily between myself Wade Rankin and Kevin Leitch. You can read everyone's input there. Kevin didn't think it was a problem with me writing about it at the time, didn't have a problem with Kathleen Sidel keeping track of autism victims, has not had a problem with all the ND bloggers that discuss the tragic ends that those with autism meet, but he does not like it that I am doing it now. I have read his criticism and think that his fundamental point, that autism is not a killer, is just wrong... as demonstrated by the fact that... well the fact that the blog illustrates in the first place. That autism directly kills a lot of people. Last weekend 12 year old Frank Marasco was pulled from his burning home. He promptly ran back inside, back up to the second floor and died. If he did not have autism, he would have had the good sense to stay out of the house. So yes... autism killed him. Autism kills the children who wander away from safety and drown. Autism killed our Ashley Brock. Autism killed Bryan Nevins. He died simply because he could not open a car door and get out of a hot car. When I wrote the initial series, Chandler was then three. He is now eight. After Ashley's death, it hit so close to home I knew I could not ignore these stories any more and I have learned to stomach these stories a little better (though not much as Web kept popping his head in my office this week and asking, "mommy, why are you crying"). Mostly because the stories are increasing in number and brutality, and they are not effecting autism policy other than a few local police departments (God bless them) and are putting in tracking systems. The horrible fact is that autism makes the world a very dangerous place for people like my son. Threats from with in and from with out. I was handed another tearful reminder of this last year as my father, being the responsible grandfather that he was, decided to take out life insurance policies for my boys. He called to tell me that he had taken a policy out for Webster, but that he could not get a policy issued for Chandler until he was ten years old. Because he had autism. Because insurance companies, whose bottom line depends on making good bets, have these things called actuarial tables, which tell them who is likely to live and who is more likely to die. And our kids, until they are ten years old, are not a good bet for the insurance company. But this does not enter into autism policy at all. I have not read anywhere, from any official source, that our children are at high risk for premature death. It is time for that to change. Three things inspired me to finally do it. The first was reading that five children had died of pertussis this year, thus triggering 'epidemic' status. Autism killed five children in April alone (autism awareness month) but the health authorities continue to yawn when our kids die. Are their lives not worth as much as those who die from viral illness? The second was someone commenting on facebook that this has been the 'summer of death'. The emotional crush of these stories that keep coming and coming has been heavy in the past few months. So I finally decided if I am going to feel like crap from all this death, I might as well try to put it to good use. The third was a conversation with another autism mom about her super fun experience. She got a call from her son's school that her son was missing. They were on the playground, there was a cloudburst, and everyone, including the aid that was supposed to be watching her son, ran inside. It took several minutes in the class room before they realized that he was missing. The boy was found, hiding in the woods sobbing, and the special ed directed acted like this was no big deal. Now parents can send this link to irresponsible educators, blaze health professionals, clueless policy makers, insensitive family members and anyone who does not quite get just what kind of risk our kids are in when they have autism. The government does not even track, in any way, how many children die (or kill others) as a result of having autism and becoming victims of their associated medical conditions, the drugs that are being used to treat them, their own lack of a sense of danger, threats from other people who can do them harm, or combinations of these factors. And as I began collecting stories this week, I began realizing that there are so many more stories than any of us though were out there. It will build slowly and we will work backward, but send stories that you come across and we will get them all up eventually. In deciding which stories to include, we basically ask the question, "if this person didn't have autism and its accompanying medical conditions, would the incident that took their life have occurred". Other parents have come forward to help me keep this archive, which is good because doing this is miserable and there is no way I could keep it up on my own. At some point I just stopped reading the stories and was cutting and pasting like a zombie. Thanks to those who have stepped forward. Bottom line, it is long past time for the autism community to face this. If we can't, then there is no way the policy makers will. And to those who don't like the blog, or see autism as a blessing... I understand where you are coming from, but I am sorry... I am just not with you on it. People with autism a precious. But autism sucks.
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Pediatr Infect Dis J. 2010 Aug 3. [Epub ahead of print] ADVERSE NEUROLOGIC REACTIONS AFTER BOTH DOSES OF PANDEMIC H1N1 INFLUENZA VACCINE WITH OPTIC NEURITIS AND DEMYELINATION.
Lapphra K, Huh L, Scheifele DW.
From the *Vaccine Evaluation Center, Department of Pediatrics, British Columbia Children' Hospital, University of British Columbia, Vancouver, British Columbia, Canada; and daggerDivision of Neurology, Department of Pediatrics, British Columbia Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada. Abstract
When a neurologic condition develops after vaccination of a patient, the causal relationship is difficult to determine. We report an unusual case in which neurologic signs occurred in a previously healthy child after both doses of H1N1 2009 influenza vaccine, culminating in bilateral optic neuritis and disseminated encephalomyelitis. A causal association is more likely with repeated injury following influenza vaccination.
PMID: 20686434 [PubMed - as supplied by publisher]
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Someone came across the 1983 US recommended vaccine schedule on the CDC's web site:  23 doses of vaccine, birth to 18 years old. Today our kids are supposed to get 70 doses. What has changed? Where was the mass death of children to justify more than tripling the number of vaccines children get? No mass deaths, just the 1985 vaccine act that gave vaccine makers immunity from killing and maiming children, and and a corrupt ACIP. And as a reminder of the massive scale of this malpractice, there is no testing, none, that tells us what giving children this vaccine schedule (or any vaccine schedule we have ever had) does to our children. This in the Age of Autism, where 1 in six children have a developmental disability or delay, where autoimmune and neurological disorders are rampant. Malpractice.
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Wow... so I am watching this hearing, and I can't believe I am watching a hearing in the US Congress. The horse is out of the barn. I don't know how Offit/Orac/Snyderman et. al. are gonna get it back in. Autism is environmental. You heard it in congress. Barbara Boxer even learned the word "epigenetics". Next session: http://www.c-spanvideo.org/program/294878-101More to come as the videos of the hearings are posted.
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The hearing will be streamed on this page tomorrow. Senators to review research on autism's enviro causes Environment and Energy Daily August 2, 2010 Gayathri Vaidyanathan, E&E reporter
The Senate Environment and Public Works Committee will meet tomorrow to probe the state of research into the environmental causes of autism and other neurodevelopment disorders.
The Children's Health Subcommittee will hear from U.S. EPA and National Institutes of Health officials on the progress of federally funded work into the causes of autism and other development disorders of the brain.
It is likely that the hearing will be a step toward reauthorizing the 2006 Combating Autism Act, which is set to expire in 2011.
Autism is thought to result from a combination of genetic and environmental factors. While the interaction of genes and mutations is somewhat known by now, little work has been done on potential environmental risk factors. There are likely to be many disparate causes leading to autism.
The incidence of autism spectrum disorders, or ASDs, is increasing in the United States, with one in every 110 children affected. Rates of attention deficit hyperactivity disorder, or ADHD, in children are also rising -- nearly 4.5 million children between 3 and 17 years of age have it, according to the U.S. Centers for Disease Control and Prevention.
The subpanel will hear from Isaac Pessah, director of the University of California, Davis, Children's Center for Environmental Health and Disease Prevention, which has received $7.5 million from EPA since 2007 for research to investigate possible environmental causes.
UC Davis is working on a project called MARBLES (Markers of Autism Risk in Babies -- Learning Early Signs) to identify early predictors of autism, whether genetic, environmental or immunologic. According to the project proposal submitted to EPA, the project will look at whether autistic children are differently exposed to metals, pesticides, polybrominated diphenylethers and other chemicals.
The work is a corollary to a long-term study called CHARGE in which UC Davis researchers are casting a wide net to catch possible environmental contributors in a group of 2- to 5-year-old autistic children. They are screening for pesticides, metals, flame retardant compounds, viruses and bacteria and pharmaceuticals.
UC Davis and other groups are also receiving money from NIH's National Institute of Environmental and Health Sciences and National Toxicology Program, and the subcommittee will hear from the program's director, Linda Birnbaum.
NIH is funding a study together with the nonprofit Autism Speaks that is enrolling mothers who already have one autistic child and are again pregnant to study exposures during fetal development.
The annual cost of caring for people with autism is $35 billion, according to Geraldine Dawson, chief scientific officer at Autism Speaks.
NIH has provided nearly $225 million for research, which Dawsom called miniscule. The funding comes from the Combating Autism Act, which authorized $7 billion for autism-related work including screening, education, intervention and research.
"President Obama has listed autism as one of three health concerns to be combated in the United States," Dawson said. "The current act is a step in the right direction, but due to the magnitude of the public health challenge that autism presents, we need a great deal more funding."
The rate of children with the disease has risen by 600 percent in the last decade, a number so dramatic it cannot be explained solely by better diagnosis, Dawson said.
Schedule: The hearing is tomorrow at 10 a.m. in 406 Dirksen.
Witnesses: Paul Anastas, assistant administrator of the Office of Research and Development, U.S. EPA; Linda Birnbaum, NIH's director of the National Institute of Environmental and Health Sciences and National Toxicology Program; Isaac Pessah, director of the UC Davis Children's Center for Environmental Health and Disease Prevention; Bruce Lanphear, senior scientist at the Child & Family Research Institute; and Mary Moen, parent.
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Kathleen Sebelius gave an interview to Moms Rising, and was asked some vaccine questions. Fran Drescher was present and asked her about spacing out vaccines: Fran never got her answer, so no... the administration is not interested in opening up a discussion on spacing out vaccines. But it is curious that Ms. Sebelius claimed that vaccines are constantly being tested for efficacy and safety. Both individually and in combination. Really? Because there is no study into the four shots (seven vaccines) that my son received at 18 months when he regressed into autism. My understanding of the process is that they do test for efficacy, but not so much for safety, and very rarely to they test combinations of vaccines for either. And of course there is no study that looks of the safety of the complete schedule in any way. The vaccine studies that they actually do are small and don't follow kids for very long. I was horrified to learn that the safety study on the Hepatitis B vaccine that Chandler reacted to when he was a new born only followed children for THREE DAYS. And of course these tests almost never include a true placebo group. Merely one version of a vaccine compared to another version of a vaccine or adjuvant. Although it was good to hear it straight from the horses mouth that the vaccine schedule is what it is partly due to convenience. Gotta get as many shots in as many kids as possible when they are in the office! Brain damage be damned. I came across an interesting movie quote in the NYT today. From a piece on the International AIDS Conference: In a lovely ironic touch, the conference hall is only a few steps from the Ferris wheel in the Orson Welles film noir classic set in postwar Vienna, “The Third Man.” On it, a cynical dealer of counterfeit drugs tells his pursuer to look down at the people below and says: “Victims? Don’t be melodramatic.... Would you really feel any pity if one of those dots stopped moving forever?” All that "constant testing" is not so much concerned with our particular little dots.  This is my little dot. His fevers, crying and constipation started three days after his first dose of Hepatitis B vaccine. I never could find a safety test that covered him.
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Over the course of the last year, Polly Tommy has proved her self, as I have previously mentioned, to have balls of steel. When threatened with having her magazine shut down if she did not fall in line with Big Brother and stop talking about those brilliant vaccines (Vaccines Are Safe, Vaccines Save Lives ® ™ PharmaCo, Inc.), and that evil Andy Wakefield (who wants children do die from measles even though he recommended the measles vaccine???) like a good little subject of the queen, she refused. Instead she went public with their threats, moved her magazine to the colonies, where the huddled masses yearning to breathe free come, and free speech is beloved, and is now upping the ante by starting her own media channel. Polly has graciously offered me a show on the channel, and I am really tempted, but as I have also recently co-founded the Center for Personal Rights to advocate for informed consent and parental choice in vaccination, I think i am over my limit on commitment. However, I have decided to become a contributor and will be having pieces there from time to time when I am able. And Kudos to the Tommy's for standing up and for bridging the autism communities across The Pond.
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At the beginning of last years pharma fund raiser "pandemic", I wrote a lengthy piece reminding readers just how bad mercury really is to humans, and just how high the mercury content in the H1N1 flu shot was. Those vaccines that public heath officials keep referring to has having 'trace amounts' of mercury. I noted that it was so mercury toxic that it was classified as hazardous material and by law must be disposed of according to hazmat rules. Now on the other side of the disease that killed ninety thousand Americans was the mildest flu in recorded history, more than $260 million dollars worth of vaccine, at least 40 million doses, are being disposed of accordingly. Being burnt in hazmat processing facilities with mercury scrubbers to keep this neurotoxin out of our environment. Which again begs the question.... When we work so hard to keep mercury out of our waterways, WHY ARE WE PUTTING THIS POISON INTO OUR BABIES ON PURPOSE!!!!! IT IS ACTUAL HAZARDOUS MATERIAL!!! IT KILLS BRAIN CELLS!!! IT CAUSES MITOCHONDRIAL DISORDERS!!!! Now I am going to be up all night worrying that the poor guy that has to burn all these vaccines is going to end up with Minamata Disease. From Occupational Health and Safety Magazine: Service Will Incinerate Unused H1N1 Vaccine Jul 23, 2010
Clean Harbors, based in Norwell, Mass., is offering the service to health care providers because multiple doses of the vaccine contain enough mercury-based Thimerosal to be treated as a hazardous waste.
Clean Harbors of Norwell, Mass., now offers H1N1 Vaccination Incineration Services that will profile, collect, and dispose of unused 2009 H1N1 vaccine for health care customers nationwide. Multiple doses of the vaccine contain enough mercury-based Thimerosal to be treated by EPA as a hazardous waste and will be incinerated. Vaccine dated at the end of 2008 and early 2009 is now at the end of its shelf life and must be disposed, according to the company.
The HHS declaration of a 2009 H1N1 Public Health Emergency expired on June 23.
"We have seen many customers in various states looking for our H1N1 disposal capabilities," John C. Kelsey, the company's vice president, Healthcare Services, said in a July 22 e-mailed reply to questions about the service. "We wanted to announce it to the larger community as we are growing our customer count related to Healthcare Services. We have done a good amount of work in this area with vaccines through our hospital Pharmaceutical Waste programs."
He said the cost varies but is "generally the same pricing as other materials requiring hazardous waste incineration. The vaccine doses are in inventory and will be shipped via DOT packages for proper disposal," Kelsey added. "We are seeing multiple truckloads per week of the vaccine now and cannot align total amounts but we do expect the need to occur from many locations as the normal pathway for outdated items." OLFA North America
Unused vaccine doses normally are returned through Reverse Distributors, but these have no value and thus must be disposed as a waste, he said, continuing, "It is good that PHER funds can be used to reimburse organizations for the disposal process."
CDC mandates proper disposal of H1N1 vaccines and allows Public Health Emergency Response (PHER) funds to be available for the disposal. Health care providers interested in the service can call 888-304-7035, e-mail healthcareservices@cleanharbors.com, or visit www.cleanharbors.com/healthcare.
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