Showing posts with label cdc. Show all posts
Showing posts with label cdc. Show all posts

The History of Vaccines That is Not Being Told to You - This Will Change The Way You Understand Vaccinations

This is and excerpt from Dr. Mercola's site and the Book: Dissolving Illusions: Disease, Vaccines, and the Forgotten History1. If you a are, or know anybody with illness or a are not in absolute perfect health, you must read this.


Sifu Marcus




Click HERE to watch the full interview!


Why This Book Was Written
Dr. Humphries' interest in this area began in 2009, when several of her patients told her that they'd been perfectly healthy until they got one vaccine or another. Prior to this, she'd been, as she says, "agnostic" about vaccination.
"I had vaccinated my dialysis patients; I, myself, was vaccinated; and I pretty much believed what I was taught in medical school," she says.
Then she started noticing that her patients were being ordered to get vaccinated on their first day of admission into the hospital—often when they had serious diseases: inflammatory diseases, heart attacks, congestive heart failure, and one patient with cancer on chemotherapy.
"My patients were getting vaccinated on their first hospital day before I even saw them, and the order had my name on it," she says. "This alerted me that there was something going on that I had not approved of.
I complained to the hospital administration about it. It was from resistance that I was met with that, ironically, led me into this path."

Countering Vaccine Arguments Led to Startling Conclusions

The conventional paradigm states that vaccines are safe and effective, and can be given to virtually anybody regardless of how sick they are.
In order to address and counter the arguments she was given for this routine policy, she had to research vaccination, which led her to discover that there is absolutely nothing in the medical literature to support vaccinating an acutely ill person.
"At some point, they called in an expert to set me straight," she says. "The arguments that I got from the experts still were not lining up with science.
My patients were acutely ill, they had inflammatory diseases, and I didn't want them vaccinated. I was told that I was confusing the nursing staff by discontinuing vaccines in my patients. That was how it all started."
Arguments often used by vaccine advocates include the oft-parroted sound byte that ‘diseases like smallpox and polio were eradicated by vaccination.’ Hence vaccines rank among the greatest medical interventions known.
As a result, she ended up researching smallpox and polio—even though it really had nothing to do with what was happening to her patients. Alas, this was when Dr. Humphries started coming to some really startling conclusions.
"In my research, I was startled [to realize] that what I found was completely counter to what I have been told and taught my entire life. I now don't believe that smallpox vaccines eradicated smallpox. I now don't believe that polio vaccines eradicated polio.
The stories are very twisted, long, and complicated, and the vaccines have changed over time. It's really easy to kind of throw up smokescreens here and there and make whatever argument one might want to, because people are so ignorant and because the story is so complicated."

The Story Behind the Smallpox Vaccine
Every vaccine has a story behind it, Dr. Humphries says. The smallpox vaccine, for example, was actually developed long before the medical establishment knew anything about the human immune system. The revelations on smallpox alone are fascinating enough to purchase this book, and is far more detailed than the summary in this article.
The vaccine was actually developed based on a rumor circulating among dairy maids. The rumor was that when a dairy maid had been infected with cowpox—which is a common infection on the udder of the cow—she would no longer be susceptible to smallpox.
The rumor was a persistent one, as rumors can be, despite the fact that there were plenty of dairy maids who developed smallpox after having cowpox. But this rumor is what led Edward Jenner to develop the first smallpox vaccine.
"Basically, it was made by scraping pus off the belly of a cow," Dr. Humphries says. "Sometimes there was some goat genetic disease in there. There was horsepox mixed in there.
There was sometimes human pox mixed in and some glycerin. They would shake it up; they would take kind of a prong, and puncture the skin several times...
What I didn't realize was that there were many people who developed serious smallpox disease and died after they were vaccinated. The severity of disease was often worse in the vaccinated than the unvaccinated.
There are statistics that show that the death rate was higher in the vaccinated than the unvaccinated."
When the smallpox vaccine was developed, there was also no way to accurately diagnose the type of pox disease a person had. It may have been chickenpox, monkeypox, or smallpox, but back then, any kind of pox disease was considered smallpox—even though the vaccine didn't actually have the human smallpox virus in it. Animal pox virus was always used. According to Dr. Humphries, it was the most contaminated vaccine that's ever been on the market.
"If you look at a town like Leicester in England, that town was noticing that they had one of the highest vaccination rates in the vaccinated world and their smallpox breakout was higher than ever," Dr. Humphries says"The people in the town had a rally. The mayor and some of the health officials were there. They all agreed that they were going to stop vaccinating... The result was quite different from the predictions.
The predictions were that there was going to be a bonfire of disease set upon the planet and that these people in Leicester were risking the health of the world by not making vaccination mandatory. But once they stopped smallpox vaccines they had the lowest rate of smallpox infection and deaths.
What we show in our book – and we show the graphs of the disease rates and the death rates – was that both of them went down precipitously after the vaccinations were stopped. That story right there tells you that vaccines were not what made the disease go away; what made the disease go away was isolation and sanitation."


Smallpox Rate
Smallpox Deaths
Smallpox Vaccine


Antibody Is the Wrong Way to Ascertain Immunity

One of the major arguments against vaccine-induced immunity is that it primarily stimulates the humoral immune system and not the cellular immune system. Antibodies are produced by the humoral immune system and then routinely measured to determine "immunity." The problem with this approach is that you can have high antibody levels and still get the disease. It’s very difficult and expensive to measure the cellular immune response, and immunologists admit that they are still in the dark about a lot of the finer points of the overall immune response.
When you use antibody titers or blood levels  to check for immunity, all you’re doing is getting a picture of what happened (you had an immune response); it doesn’t tell you whether you’re going to be immune in the future, because antibodies are only one aspect of the immune response, and in some cases are not even necessary to easily combat the sickness and become immune.
For example, those with agammaglobulinemia—a disease where you cannot make antibodies — can get infected with measles, recover uneventfully, and still respond to subsequent challenges of the virus in a normal healthy fashion and not get sick. These individuals will have lifelong immunity to measles, the same as someone without agammaglobulinemia.
Traditionally, the way immunity is determined is to do a test that measures antibodies, which is the humoral immune system. But there’s no good way to assess the cellular immune system. It’s a really imprecise science at best. As Dr. Humphries notes:
"It's not only imprecise; sometimes it's downright inaccurate. You can have very high antibody levels, like numerous case reports of people who have hugely high antibody levels for tetanus, or normal antibodies, and have gotten some of the worst cases of tetanus. I have papers that show that people without antibody for polio have actually been able to respond to the virus as if they were already immune. The antibody really is a real wrong roadmap to look at to tell what's really going on. Sometimes there's correlation, but it's certainly not a given."

The Story Behind the Polio Vaccine

The other prime argument for the justification and support of today’s highly aggressive vaccination program is the alleged success of the polio vaccine. But here again, the historical perspective fails to support the vaccination paradigm.
"The story behind polio is absolutely fascinating when you look at the politics that went on researching the vaccine, and how scientists were fired if they disagreed with the program going on through the National Foundation of Infantile Paralysis (NFIP) in the late 1940s and early 1950s. That was the vaccine that Jonas Salk developed," Dr. Humphries says.
Before the Salk vaccine became available, if you were admitted to the hospital any doctor could diagnose you with polio based on two physical examinations within 24 hours, to check for paralysis in one or more muscle groups. We now know that a number of viruses can cause paralysis, but back then, all instances were thought to be due to polio virus. When the polio vaccine was developed, a problem emerged. Swedish scientists were trying to tell the US scientists that formaldehyde inactivation was not going to work as planned.
Their warning, however, fell on deaf ears. This was unfortunate, as they turned out to be correct. Live poliovirus, which was put in an injectable vaccine, would appear to be inactivated right after it was made, but sometimes it would "resurrect" in the vial... In essence, the formaldehyde did not kill off all the polioviruses in these vaccines, which led to live polio viruses being injected. As a result, more people developed paralysis from the vaccine in 1955 than would have developed it from a wild, normal natural poliovirus.
Something had to be done to make it appear as though the vaccine was working. So what they did was change the diagnostic criteria for polio. Sadly this is a very common practice in medicine. When the observations don’t fit your expectations, change or rig the system so that they do. With polio, the original criteria was two examinations within 24 hours. This was changed to two examinations within 60 days. This was helpful in cooking the books, because within 60 days, most people recover from their bout with poliomyelitis.
"All those people who were formerly called polio were no longer categorized as polio because they recovered from their paralysis within that time," Dr. Humphries explains.
Then there was the issue of testing. Prior to the vaccine, there was no testing done on blood or stool samples. After the vaccine came along, there was an epidemic in Michigan around 1958. About 2,000 people were diagnosed with polio. In disbelief over the outbreak, serological testing was done, and they discovered that the polio virus was found in only a small minority—about one-quarter of those who displayed symptoms of infection. Interestingly, in the remainder they discovered a different virus or no virus at all! And, subsequently, those patients were no longer "counted" as having polio.
"So simply by doing the diagnostic testing and changing the diagnostic criteria, the rates of polio plummeted, whether or not there was ever a vaccine. These were the kind of things that were going on back then," Dr. Humphries says.

Oral Polio Vaccine Propagates Transmission of Vaccine Virus

It’s important to realize that the injected polio vaccine does nothing to prevent transmission of the virus, and after an oral polio vaccine you become a reservoir of virus that can mutate or combine with other bowel viruses, creating new strains that are often more virulent to those around you. According to Dr. Humphries, the only thing the injectable vaccine theoretically does is give you some blood immunity, similar to tetanus. This means it is only going to be effective if your blood meets the virus before the virus meets your nervous system.
Once vaccine makers realized just how difficult it was to inactivate the polio virus, and many people ended up contracting polio from the vaccine, they decided to abandon the injectable polio vaccine and create an oral vaccine instead, which is more similar to the natural route of infection. Again, controversy ensued. The oral vaccine did interrupt transmission of the wild type virus, but it propagated transmission of the vaccine virus instead.
"The fact of the matter is that you can attenuate a virus all you want, which means that you pass it through different animals to make it mutate enough that it's not quite as lethal or virulent at some point. But once you put that vaccine or that virus back into its natural host, it mutates back to the way it was," Dr. Humphries explains.
"You can give a baby an oral polio vaccine and it can be attenuated. But even in the vial, before you give it to that baby, those viruses are starting to revert back to their former problematic state. And then once the baby swallows that, the baby will generate some immunity in the intestine. But what's going to come out of that baby is going to be mutated vaccine virus. Oftentimes this is problematic, especially in people who are immunosuppressed."
In the 1990s the US quit using the oral vaccine, and switched back to the injectable vaccine. To address the hazards of injecting improperly or inadequately inactivated polio virus, certain adjustments to the formulation were made. Modern polio vaccines are propagated and inactivated differently from earlier versions, and different countries also use different strains of the polio virus. Older polio viruses used to contain three strains of the virus. Today, some countries will only use one or two.

Polio Was 'Eradicated' NOT by the Vaccine But Through Redefinition

As noted by Dr. Humphries, it's very easy to defeat the polio vaccine argument, as most incidences of polio disappeared because the disease was redefined—not because there was an actual change in disease prevalence. In fact, it could be argued that the vaccine did more harm than good, since some versions caused polio, and others propagated new mutated strains of the virus. According to Dr. Humphries, at one point, the only polio cases in the US were vaccine-induced. Yet even though there are no cases of wild polio being discovered, the polio vaccine remains part of the US vaccine program...
"Even today, you can just go on to the CDC website and the Morbidity and Mortality Weekly Report (MMWR). You can see that cases of polio in this country by and large occur when people get the oral vaccine in another country and then come here. When they say that polio is only a plane ride away, the truth is that disease from polio vaccine is also a plane ride away... Like I said, the injected vaccines do not interrupt propagation of the virus. If somebody comes to this country who has recently had an oral polio vaccine and he's shedding a highly virulent strain, people in this country can start passing it around."

Polio Epidemic Historically Related to Increase in Sugar Consumption

Here's another interesting tidbit that no one ever talks about: In the past, it has sometimes been suggested that a large part of the polio epidemic was related to increases in sugar consumption. Dr. Benjamin Sandler wrote an entire book about this, and Dr. Humphries refers to his work in her book as well. She explains the connection as follows:
"Polio's an enterovirus [i.e. a virus that enters the body through the gastrointestinal tract and thrives there]. The integrity and the flora population in your bowel is extremely important when it comes to dealing with any kind of bowel infection. A diet that's high in sugar is going to 1) impair your cell-mediated immune system and 2) trash your gut flora... [It was] shown that in populations who cut back on their sugar intake, the rates of polio plummeted... But it was so unbelievable that nobody really listened to him.
It was the same as when Dr. Frederick Klenner tried to say that he cured 100 percent of patients with intravenous vitamin C and [it] just didn't register. The... low-sugar diet was very effective because of the effect it has on the immune system and on the bowel flora. The same with dichlorodiphenyltrichloroethane (DDT); DDT really trashes the bowel, the intestinal walls, and the flora.... Not only can DDT give you all the symptoms of polio all by itself, it can also make the poliovirus much more virulent and active in the body for the same reason: it disturbs the normal function of the bowel."
DDT exposure has also been linked to Alzheimer's disease, and it's worth noting that the contemporary equivalent of DDT, glyphosate, according to Dr. Don Huber, professor emeritus at Purdue University, is far more toxic than DDT. It definitely has been shown to decimate your microbiome, and glyphosate preferentially kills bacteria known to be beneficial for human health.

'You Cannot Dabble in the Topic of Vaccination'

Dr. Humphries left a successful practice making $300,000 a year to be a poorly paid researcher. For her it was worth it, because her integrity wouldn't allow her to turn a blind eye to what she knew to be wrong.
"If you want to make these [vaccine] arguments, we have to have information and we have to have knowledge. We have to understand the history, the medical literature, the biology, the chemistry, the physiology, and the immunology. That is not easy. You cannot dabble in the topic of vaccination. If you do, you're likely going to be toppled by the pro-vaccine lobby because they're doing their homework.
I felt it was more important to do my homework and make these arguments that I wanted to make... I do lectures if people invite me. I have toured through Scandinavia. Our book has been translated into two different languages [Spanish and German]... Right now I'm really immersed in the topic of infant immunity because there is so much information that has just come out in the past few years that, in my opinion, turns the vaccine paradigm for infants completely on its head.
Instead of arguing about any particular vaccine, if you understand the way the infant immune system is designed, you can automatically see that if you were going to toss any kind of a vaccine in there, you might give them some short-term immunity, but you're also going to change their immune systems so that it can't function the way it was designed to function... The arguments against vaccines when you really understand the infant immune system I think are irrefutable."

Science of Epigenetics Changes Everything Yet Again...

Epigenetics is another field where biology is being turned on its head and all the old paradigms are being tossed out. Epigenetic science now tells us that our genes are NOT our destiny, and the problem is that once you start to epigenetically tinker with the infant immune system, you are basically depositing what Dr. Humphries refers to as "little cluster bombs" that will eventually "explode into a big problem." As an example, she cites a study by Nikolaj Orntoft, in which African girls were injected with a tetanus vaccine to see which genes might be upregulated or downregulated. What they found is that there's really no way to predict which genes will be affected.
So not only will each individual have a unique response to any given vaccine, based on their current health status, we're also epigenetically predisposed to respond differently in terms of the side effects we might develop. This means that having a vaccine compensation table for reimbursement for vaccine damage is nonsensical as we're bound to have different genes upregulated after vaccines are given.
"We can have cancer genes upregulated, or autoimmune diseases upregulated. This has been shown in modern literature that used these highly sophisticated gene techniques to actually watch what happens after the vaccine is injected. I think this is really powerful information to show that, when vaccines started, they knew nothing about the immune system. Then scientists knew something about the immune system, but now we know about the genetics of the immune system and the epigenetics of the immune system, and that's got to be taken into account..."

Most Doctors Are Completely Uninformed, Which Means You Cannot Make an Informed Choice

Dr. Humphries stresses the importance of "thinking long and hard" about how much information you've been given beforeyour child is given a vaccine.
“[Vaccines] can have tumorigenic kidney cells of a cocker spaniel in it. It can have human fetal cells with retroviruses. [It can have] aluminum, which is one of the most horrible things to inject into any sort of life form, especially into a muscle... Parents really need to know that their doctors are not informed and therefore they cannot give informed consent, and that they really need to think about it because you cannot unvaccinate.
The fear of, “Oh, what if my child gets a disease”—that’s where knowing the history is really important because what we’re talking about is under which conditions people become susceptible . That’s really more important than transmission. Because, yes, measles transmits very rapidly through the population, but it actually has a lot of benefits to the immune system—so much so that they’re using it to treat cancer today.”
We really need to understand each disease – what the risk of it is, how it's transmitted, what the vaccine effectiveness is, and what the risks are. Dr. Humphries also notes that the human body is designed in such a perfect way that there is a system in place to handle just about anything that happens to it, provided we've treated our body properly.
"Babies who come into this world in a normal and natural way, who are breastfed for an appropriate amount of time, that's the best protection you could ever give to your baby's immune system or brain. Consider that when the fear starts to creep in. If you're breastfeeding your baby, you're already giving the most powerful thing on the planet that can be given to that baby," she says.

More Information

People have been scared into believing vaccines are the answer to prevent disease, but when you look at the historical evidence, the arguments used simply fall apart. There's just no question that improving your innate immune system—through reducing sugar and processed foods in your diet, improving your gut flora, leading a healthy lifestyle, and having adequate vitamin D levels, ideally through sensible sun exposure,—will provide a far more effective immune response and virtually eliminate any risk of developing a life threatening infection.
The key is to have the courage to trust in this truth—that your body is designed to maintain health. Its natural course and direction is to be healthy not sick. If you have a healthy lifestyle, exposure to nearly all of these infectious agents will ultimately make you healthy and stronger. This is similar to exercise, which actually tears your body down to make it stronger. Nature actually knows what it's doing, whereas putting chemicals into your body based on human theories (or rumors!) that are oftentimes completely wrong, is unlikely to produce better results. As noted by Dr. Humphries:
"We have a highly profitable, lucrative religion that involves the government, industry, and academia. That religion is vaccination. People believe in vaccines. They'll tell you, they believe in vaccines. But you ask them what they know about vaccines and it will be almost nothing. In fact the people who argue the loudest usually know the least when it comes to trying to convince you to take the vaccine. That's been my experience.
Medical schools are bereft of information on the history of vaccination, on the contents of them, and the potential problems. We have the go-to doctors, like Dr. Paul Offit, teaching doctors how to talk to vaccine-refusing parents. We have doctors like Dr. Robert Jacobson putting out PowerPoint presentations to give to doctors, literally telling them to persuade the parents rather than to inform them...
Doctors are really being systematically brainwashed. Not only that, but if doctors do start to see problems... wake up to it; do their own research, and buck the system, they risk being treated the way I was. I was well respected through the entire state of Maine. People were referring their patients to me. My colleagues would come to me with their medical problems... But once I started to argue against the practice of vaccination, I was automatically tossed into the category of a quack..."
To learn more, I couldn’t more highly recommend Dr. Humphries excellent book, Dissolving Illusions: Disease, Vaccines, and the Forgotten Historyavailable in paper back and Kindle on Amazon. You can also find more information on the book’s website, dissolvingillusions.com.  I have read it cover to cover and plan on doing so again as there are loads of powerful information that helps combat the blindly foolish acceptance of nearly all media and professionals on the value of vaccinations.
Other Unreasonable Happiness Posts You Would Be Interested In

Get Better Now!... Living Mastery
Show Archives:




Did you find this information useful?
Then pay it forward. Help my Scholarship Students with their tuition and allow me to create more of my Free Programs and Shows for everyone. How? Just click below to Donate, any amount is greatly appreciated and it all goes to a good cause.






Thank You,
Sifu Marcus Lovemore

Vaccine Facts Instead of Fear Mongering and Insults Part 4 & 5


By Russel L. Blaylock, M.D

Dr. Rapin expressed her concern over public opinion when this information eventually gets out. She says (page 197), they are going to be captured by the public and we had better make sure that "a) We council them carefully and b) that we pursue this because of the very important public health and public implications of the data." "The stakes are very high ... ," Dr. Johnson adds.
From this how can one conclude anything other than the fact that at least these scientists were extremely concerned by what was discovered by this study examining the vaccine safety datalink material? They were obviously terrified the information would leak out to the public. Stamped in bold letters at the top of each page of the study were the words "DO NOT COPY OR RELEASE" and "CONFIDENTIAL." 
This is not the wording one would expect on a clinical study of vaccine safety. Instead, you would expect it on top-secret NSA or CIA files. Why was this information being secreted?

Vaccine Confidential

The answer is obvious: It might endanger the vaccine program and indict the federal regulatory agencies for ignoring this danger for so many years. Our society is littered with millions of children who have been harmed in one degree or another by this vaccine policy. In addition, let us not forget the millions of parents who have had to watch helplessly as their children have been destroyed by this devastating vaccine program.
Dr. Bernier, on page 198, says, "The negative findings need to be pinned down and published." Why was he so insistent that the "negative findings" be published? Because he said, "Other less responsible parties will treat this as a signal." By that he means, a signal of a problem with thimerosal-containing vaccines. 
From this, I assume he wants a paper that says only that nothing was found by the study. As we shall see, he gets his wish. 
In addition, on page 198, Dr. Rapin notes that a study in California found a 300 percent increase in autism following the introduction of certain vaccines. She quickly attributes this to better physician recognition. Two things are critical to note at this point.
  1. Dr. Rapin makes this assertion or better physician recognition without any data at all, just her wishful thinking. If someone pointing out the dangers of vaccines were to do that, she would scream "junk science."
  2. Dr. Weil, on page 207, attacks this reasoning when he says, "The number of dose-related relationships are linear and statistically significant. You can play with this all you want. They are linear. They are statistically significant." In other words, how can you argue with results that show a strong dose/response relationship between the dose of mercury and neurodevelopmental outcomes? The higher the mercury levels in the children, the greater the number of neurological problems.
He continues by saying that the increase in neurobehavioral problems is probably real. He tells them that he works in a school system with special education programs and "I have to say the number of kids getting help in special education is growing nationally and state by state at a rate not seen before. So there is some kind of increase. We can argue about what it is due to." (page 207)

The "Eureka" Moment

Dr. Johnson seems to be impressed by the findings as well. He says on page 199, "This association leads me to favor a recommendation that infants up to two-years-old not be immunized with thimerosal containing vaccines if suitable alternative preparations are available." 
Incredibly, he quickly adds, "I do not believe the diagnosis justified compensation in the Vaccine Compensation Program at this point." It is interesting to note that one of our experts in attendance is Dr. Vito Caserta, the Chief Officer for the Vaccine Injury Compensation Program. 
At this point, Dr. Johnson tells the group about his concerns for his own grandchild. On page 200, he says, "Forgive this personal comment, but I got called out at 8:00 for an emergency call and my daughter-in-law delivered a son by c-section. Our first male in the line of the next generation and I do not want that grandson to get a Thimerosal containing vaccine until we know better what is going on. It will probably take a long time. In the meantime, and I know there are probably implications for this internationally, but in the meanwhile I think I want that grandson to only be given Thimerosal-free vaccines. 
So, we have a scientist sitting on this panel who will eventually make policy concerning all of the children in this country, as well as other countries, who is terrified about his new grandson getting a thimerosal-containing vaccine, but is not concerned enough about your children to speak out and try to stop this insanity. He allows a cover up to take place after this meeting adjourns and remains silent. 
It is also interesting to note, although he feels the answers will be a long time coming, in the meantime, his grandson will be protected. 
Nevertheless, the American Academy of Pediatrics, American Academy of Family Practice, AMA, CDC and every other organization will endorse these vaccines and proclaim them to be safe as spring water, but Dr. Johnson and some of the others will keep their silence.

It is only during the last day of the conference that we learn that most of the objections concerning the positive relationship between thimerosal-containing vaccines and ADD and ADHA were bogus. For example, Dr. Rapin on page 200 notes that all children in the study were below age 6 and that ADD and ADHD are very difficult to diagnose in pre-schoolers. She also notes that some children were followed for only a short period.

Dr. Stein adds that in fact the average age for diagnosis of ADHD was 4 years and 1 month. A very difficult diagnosis to make and that the guidelines published by the American Academy of Pediatrics limits diagnosis to 6 to 12 year olds. Of course, he was implying that too many were diagnosed as ADHD. Yet, a recent study found that the famous Denmark study that led to the announcement by the Institute of Medicine that there was no relationship between autism and the MMR vaccine, used the same tactic. They cut off the age of follow-up at age six.

It is known that many cases appear after this age group, especially with ADD and ADHD. In fact, most learning problems appear as the child is called on to handle more involved intellectual material. Therefore, the chances are they failed to diagnose a number of cases by stopping the study too early.
Several of the participants tried to imply that autism was a genetic disorder and therefore could have nothing to do with vaccines. Dr. Weil put that to rest with this comment, "We don't see that kind of genetic change in 30 years." In other words, how can we suddenly see a 300% increase in a genetically related disorder over such a short period? It is also known that there are two forms of autism, one that is apparent at birth and one that develops later in childhood. The former has not changed in incidence since statistics have been kept; the other is epidemic.

In one interesting exchange, which ends up being their justification for the view that mercury is of no danger in children vaccinated with vaccines containing thimerosal, involves two studies in children born to mothers consuming high intakes of mercury contaminated fish. One study reported in the journal Neurotoxicology, examined children living in the Republic of Seychelles. In this study, they examined the effect of prenatal exposure to mercury through the mother's consumption of fish high in methylmercury.

A battery of developmental milestone tests were done and no adverse effects were reported in the study reported by Dr. Clarkson and co-workers, the very same person in this conference. He never mentions that a follow-up study of these same children did find a positive correlation between methylmercury exposure and poor performance on a memory test. In a subsequent study of children living on the Faroe Islands exposed to methylmercury, researchers did find impairments of neurodevelopment. This experiment was done by scientists from Japan.

Throughout the remainder of this discussion, Dr. Clarkson and others refer to these two studies. When they are reminded that the Faroe study did find neurological injury to the children, they counter by saying that this was prenatal exposure to mercury and not after birth as would be seen with vaccination. The idea being that prenatally the brain is undergoing neural formation and development making it more vulnerable. As I have mentioned this rapid brain growth and development continues for two years after birth and even at age 6 years the brain is only 80% formed.

Dr. Clarkson keeps referring to the Seychelles study, which demonstrated that the children reached normal neurodevelopmental milestones as shown by a number of tests. Dr Weil points out on page 216 that this tells us little about these children's future brain function. He says, "I have taken a lot of histories of kids who are in trouble in school. The history is that developmental milestones were normal or advanced and they can't read at second grade, they can't write at third grade, they can't do math in the fourth grade and it has no relationship as far as I can tell to the history we get of the developmental milestones. So I think this is a very crude measure of neurodevelopment."

In other words, both of these studies tell us nothing about the actual development of these children's brain function except that they reached the most basic of milestones. To put this another way, your child may be able to stack blocks, recognize shapes and have basic language skills but later in life they could be significantly impaired when it came to higher math, more advanced language skills (comprehension) and ability to compete in a very competitive intellectual environment, like college or advanced schooling. Their future would be limited to the more mundane and intellectually limited jobs.

Post-natal brain development, that is from birth to age six or seven, involves the fine tuning of synaptic connections, dendritic development and pathway refinement, all of which prepare the brain for more complex thinking. These brain elements are very sensitive to toxins and excessive immune stimulation during this period. This is never mentioned in this conference.

In addition, it must be remembered that the children in these two studies were exposed only to methylmercury and not the combined neurotoxic effect of mercury, aluminum and excessive and chronic activation of the brain's immune system (microgia). This is what makes it so incredible, that several of these "vaccinologists" and so-called experts would express doubt about the "biological plausibility" of thimerosal or any vaccine component causing neurodevelopmental problems. The medical literature is exploding with such studies. The biological plausibility is very powerful.

Mercury, for example, even in low concentrations, is known to impair energy production by mitochondrial enzymes. The brain has one of the highest metabolic rates of any organ and impairment of its energy supply, especially during development, can have devastating consequences. In addition, mercury, even in lower concentrations, is known to damage DNA and impair DNA repair enzymes, which again, plays a vital role in brain development. Mercury is known to impair neurotubule stability, even in very low concentrations. Neurotubules are absolutely essential to normal brain cell function. Mercury activates microglial cells, which increases excitotoxicity and brain free radical production as well as lipid peroxidation, central mechanisms in brain injury. In addition, even in doses below that which can cause obvious cell injury, mercury impairs the glutamate transport system, which in turn triggers excitotoxicity, a central mechanism in autism and other neurological disorders. Ironically, aluminum also paralyzes this system.

On page 228, we see another admission that the government has had no interest in demonstrating the safety of thimerosal-containing vaccines despite over 2000 articles showing harmful effects of mercury. Here we see a reference to the fact that the FDA "has a wonderful facility in Arkansas with hundreds of thousands of animals" available for any study needed to supply these answers on safety. The big question to be asked is -So, why has the government ignored the need for research to answer these questions concerning thimerosal safety? You will recall in the beginning the participants of this conference complained that there were just so few studies or no studies concerning this "problem."

Again, on page 229 Dr, Brent rails about the lawsuit problem. He tells the others that he has been involved in three lawsuits related to vaccine injuries leading to birth defects and concluded "If you want to see junk science, look at those cases..." He then complains about the type of scientists testifying in these cases. He adds, "But the fact is those scientist are out there in the United States." In essence, he labels anyone who opposes the "official policy" on vaccines as a junk scientist. We have seen in the discussion who the "junk scientists" really are.

Knowing that what they have found can cause them a great deal of problems he adds, "The medical/legal findings in this study, causal or not, are horrendous... If an allegation was made that a child's neurobehavioral findings were caused by thimerosal-containing vaccines, you could readily find a junk scientist who will support the claim with 'a reasonable degree of certainty." On page 229 he then admits that they are in a bad position because they have no data for their defense. Now, who are the junk scientists?

Is a "real scientist" one who has no data, just wishful thinking and a "feeling" that everything will be all right? Are real scientists the ones who omit recognized experts on the problem in question during a conference because it might endanger the "program?" Or are they the ones who make statements that they don't want their grandson to get thimerosal-containing vaccines until the problem is worked out, but then tell millions of parents that the vaccines are perfectly safe for their children and grandchildren?

Dr. Meyers on page 231 put it this way, "My own concern, and a couple of you said it, there is an association between vaccines and outcomes that worries both parents and pediatricians." He sites other possible connections to vaccine-related neurobehavioral and neurodevelopmental problems including the number of vaccines being given, the types of antigens being used and other vaccine additives.

Dr. Caserta tells the group that he attended the aluminum conference the previous year and learned that often metals could act differently in biological systems than as an ion. This is interesting in the face of the finding that fluoride when combined to aluminum forms a compound that can destroy numerous hippocampal neurons at a concentration of 0.5 ppm in drinking water. It seems that aluminum readily combines with fluoride to form this toxic compound. With over 60% of communities having fluoridated drinking water this becomes a major concern.

It has also been learned that fluoroaluminum compounds mimic the phosphate and can activate G-proteins. G-proteins play a major role in numerous biological systems, including endocrine, neurotransmitters, and as cellular second messengers. Some of the glutamate receptors are operated by a G-protein mechanism.

Over the next ten to fifteen pages, they discuss how to control this information so that it will not get out and if it does how to control the damage. On page 248 Dr. Clements has this to say:

"But there is now the point at which the research results have to be handled, and even if this committee decides that there is no association and that information gets out, the work has been done and through the freedom of information that will be taken by others and will be used in other ways beyond the control of this group. And I am very concerned about that as I suspect that it is already too late to do anything regardless of any professional body and what they say."
In other words, he wants this information kept not only from the public but also from other scientists and pediatricians until they can be properly counseled. In the next statement he spills the beans as to why he is determined that no outsider get hold of this damaging information. He says,
"My mandate as I sit here in this group is to make sure at the end of the day that 100,000,000 are immunized with DTP, Hepatitis B and if possible Hib, this year, next year and for many years to come, and that will have to be with thimerosal containing vaccines unless a miracle occurs and an alternative is found quickly and is tried and found to be safe."
This is one of the most shocking statements I have ever heard. In essence, he is saying, I don't care if the vaccines are found to be harmful and destroying the development of children's brains, these vaccines will be given now and forever. His only concern by his own admission is to protect the vaccine program even if it is not safe. Dr. Brent refers to this as an "eloquent statement."On page 253, we again see that these scientists have a double standard when it comes to their children and grandchildren. Dr. Rapin raises the point about a loss of an IQ point caused by thimerosal exposure. She says,"an we measure the IQ that accurately, that this one little point is relevant? Then she answers her own question by saying, "Even in my grandchildren, one IQ point I am going to fight about." Yet, they are saying in unison, in essence-TO HELL WITH YOUR CHILDREN- to the rest of America.

It is also interesting that they bring up the history of lead as a neurobehavioral toxin. Dr. Weil noted that the neurotoxicologists and regulatory agencies have lowered the acceptable level from 10 to 5 ug. In fact, some feel that even lower levels are neurotoxic to the developing brain. Before the toxicologists began to look at lead as a brain toxin in children most "experts" assumed it was not toxic even at very high levels. Again, it shows that "experts" can be wrong and it is the public who pays the price.

Dr. Chen on page 256 expresses his concern about this information reaching the public. He remarks, "We have been privileged so far that given the sensitivity of information, we have been able to manage to keep it out of, lets say, less responsible hands..." Dr. Bernier agrees and notes, "This information has been held fairly tightly." Later he calls it "embargoed information" and "very highly protected information."

That they knew the implications of what they had discovered was illustrated by Dr. Chen's statement on page 258. He says, "I think overall there was this aura that we were engaged in something as important as anything else we have ever done. So I think that this was another element to this that made this a special meeting." You may remember, Dr. Weil emphasized that the data analysis left no doubt that there was a strong correlation between neurodevelopmental problems and exposure to thimerosal-containing vaccines. So if they understood the importance of this finding and this was the most important thing they have ever dealt with-why was this being kept from the public? In fact, it gets even worse.

Just so you will not doubt my statement that this audience of experts was not objective, I give you the words of Dr. Walter Orenstein, Director of the National Immunization Program at the CDC, on page 259. He tells the group, "I have seen him (Verstraeten) in audience after audience deal with exceedingly skeptical individuals..." "Exceedingly skeptical individuals" does that sound like objective scientists who wanted to look at the data with a clear mind or were they scientists who were convinced before the meeting was held that there was no danger to children from thimerosal or any other vaccine component?

In one of the closing remarks by Dr. Bernier (page 257) he says, "the other thing I was struck by was the science," meaning the science expressed by the attendees of the meeting. Then Dr, Orenstein adds, "I would also like to thank Roger Bernier who pulled off this meeting in rather short notice..." Here is a meeting that has been called one of the most important they have ever dealt with and we learn that it was pulled off on short notice. In addition, we were told that the results of this meeting would lead to eventual vaccine policy.
He then has the nerve to add:

"In a sense this meeting addresses some of the concerns we had last summer when we were trying to make policy in the absence of a careful scientific review. I think this time we have gotten it straight."
Well, I hate to be the one to break the news, but he didn't get it straight. There was little or no science in this meeting; rather it was composed of a lot of haggling and nit picking over epidemiological methodology and statistical minutia in an effort to discredit the data without success. In fact, the so-called mercury experts admitted they had to do some quick homework to refresh their memories and learn something about the subject.

Conclusions

This top secret meeting was held to discuss a study done by Dr. Thomas Verstraeten and his co-workers using Vaccine Safety Datalink data as a project collaboration between the CDC's National Immunization Program (NIP) and four HMOs. The study examined the records of 110,000 children. Within the limits of the data, they did a very through study and found the following:

  1. Exposure to thimerosal-containing vaccines at one month was associated significantly with the misery and unhappiness disorder that was dose related. That is, the higher the child's exposure to thimerosal the higher the incidence of the disorder. This disorder is characterized by a baby that cries uncontrollably and is fretful more so than that see in normal babies.
  2. Found a nearly significant increased risk of ADD with 12.5ug exposure at one month.
  3. With exposure at 3 months, they found an increasing risk of neurodevelopmental disorders with increasing exposure to thimerosal. This was statistically significant. This included speech disorders.
It is important to remember that the control group was not children without thimerosal exposure, but rather those at 12.5ug exposure. This means that there is a significant likelihood that even more neurodevelopmental problems would have been seen had they used a real control population. No one disagreed that these findings were significant and troubling. Yet when the final study was published in the journal Pediatrics Dr. Verstraeten and co-workers reported no consistent associations were found between thimerosal-containing vaccine exposure and neurodevelopmental problems. In addition, he list himself as an employee of the CDC, not disclosing the fact that at the time the article was accepted, he worked for GlaxoSmithKline, a vaccine manufacturing company.

So how did they do this bit of prestidigitation? They simply added another HMO to the data, the Harvard Pilgrimage. Congressman Dave Weldon noted in his letter to the CDC Director that this HMO had been in receivership by the state of Massachusetts because its records were in shambles. Yet, this study was able to make the embarrassing data from his previous study disappear. Attempts by Congressman Weldon to force the CDC to release the data to an independent researcher, Dr. Mark Geier, a researcher with impeccable credentials and widely published in peer-reviewed journals, have failed repeatedly.

It is obvious that a massive cover-up is in progress, as we have seen with so many other scandals-fluoride, food-based excitotoxins, pesticides, aluminum and now vaccines. I would caution those critical of the present vaccine policy not to put all their eggs in one basket, that is, with thimerosal as being the main culprit. There is no question that it plays a major role, but there are other factors that are also critical, including aluminum, fluoroaluminum complexes, and chronic immune activation of brain microglia.

In fact, excessive, chronic microglial activation can explain many of the effects of excessive vaccine exposure as I point out in two recently published articles. One property of both aluminum and mercury is microglial activation. With chronic microglial activation large concentrations of excitotoxins are released as well as neurotoxic cytokines. These have been shown to destroy synaptic connections, dendrites and cause abnormal pathway development in the developing brain as well as adult brain.

In essence, too many vaccines are being given to children during the brain's most rapid growth period. Known toxic metals are beings used in the vaccines that interfere with brain metabolism, antioxidant enzymes, damage DNA and DNA repair enzymes and trigger excitotoxicity. Removing the mercury will help but will not solve the problem because overactivation of the brain's immune system will cause varying degrees of neurological damage to the highly-vulnerable developing brain.

References For This Article

  1. Lorscheider,FL; Vimy,MJ; Pendergrass,JC; Haley,BE. Mercury vapor exposure inhibits tubulin binding to GTP in rat brain: A molecular lesion also present in human Alzheimer brain From: FASEB J. 9(4): A-3845. FASEB Annual Meeting, Atlanta, Georgia, 10 March 1995.
  2. Grandjean P, Budtz-Jorgensen E, White RF, Jorgensen PJ, Weihe P, Debes F, Keiding N Methylmercury exposure biomarkers as indicators of neurotoxicity in children aged 7 years. From: Am J Epidemiol 1999 Aug 1;150(3):301-5.
  3. Albers JW, Kallenbach LR, Fine LJ, Langolf GD, Wolfe RA, Donofrio PD, Alessi AG, Stolp-Smith KA, Bromberg MB Neurological abnormalities associated with remote occupational elemental mercury exposure. Ann Neurol 1988 Nov;24(5):651-9.
  4. Aschner M, Lorscheider FL, Cowan KS, Conklin DR, Vimy MJ, Lash LH Metallothionein induction in fetal rat brain and neonatal primary astrocyte cultures by in utero exposure to elemental mercury vapor (Hg0). From: Brain Res 1997 Dec 5;778(1):222-32.
  5. Soederstroem S, Fredriksson A, Dencker L & Ebendal T The effect of mercury vapour on cholinergic neurons in the fetal brain: studies on the expression of nerve growth factor and its low- and high-affinity receptors. Developmental Brain Research 85(1):96-108 (1995).
  6. Drasch G, Schupp I, Hofl H, Reinke R & Roider G. Mercury burden of human fetal and infant tissues. Eur J Pediatr 153:607-610 (1994).
  7. Szucs A, Angiello C, Salanki J, Carpenter DO Effects of inorganic mercury and methylmercury on the ionic currents of cultured rat hippocampal neurons. Cell Mol Neurobiol 1997 Jun;17(3):273-88.
  8. Low-Level Exposure to Methylmercury Modifies Muscarinic Cholinergic Receptor Binding Characteristics in Rat Brain and Lymphocytes: Physiologic Implications and New Opportunities in Biologic Monitoring Teresa Coccini,1 Giovanna Randine,2 Stefano M. Candura,1,3 Rossella E. Nappi,2,3 Leon D. Prockop,4 and Luigi Manzo.
  9. Sorg O, Schilter B, Honegger P, Monnet-Tschudi F Increased vulnerability of neurones and glial cells to low concentrations of methylmercury in a prooxidant situation. Acta Neuropathol (Berl) 1998 Dec;96(6):621-7.
  10. Liang YX, Sun RK, Sun Y, Chen ZQ, Li LH Psychological effects of low exposure to mercury vapor: application of a computer-administered neurobehavioral evaluation system. Environ Res 1993 Feb;60(2):320-7.
  11. Sundberg J, Jonsson S, Karlsson MO, Oskarsson A Lactational exposure and neonatal kinetics of methylmercury and inorganic mercury in mice. Toxicol Appl Pharmacol 1999 Jan 15;154(2):160-9.
  12. Inouye M., Murao K., Kajiwara Y., Behavorial and neuropathological effects of prenatal methyl Mercury exposure in mice.. Neurobehav.Toxicol Teratol. ,1985:7;227-232.
  13. Koos et al., Mercury toxicity in pregnant women, fetus and newborn infant. Am J Obstet And Gynecol., 1976:126;390-409.
  14. Khera et al., Teratogenic and genetic effects of Mercury toxicity. The biochemistry of Mercury in the environment. Nriagu, J.O.Ed Amsterdam Elsevier, 503-18,1979.
  15. Drasch G, Schupp I, Hofl H, Reinke R, Roider G Mercury burden of human fetal and infant tissues. Eur J Pediatr 1994 Aug;153(8):607-10.
  16. Yoshida M, Yamamura Y, Satoh H Distribution of mercury in guinea pig offspring after in utero exposure to mercury vapor during late gestation Arch Toxicol 1986 Apr;58(4):225-8.
  17. Yuan,Y; Atchison,WD. Comparative effects of inorganic divalent mercury, methylmercury and phenylmercury on membrance excitability and synaptic transmission of CA1 neurons in hippocampal slices of the rat Neurotoxicology. 14(2):403-411, 1994.
  18. Desi I, Nagymajtenyi L, Schulz H Effect of subchronic mercury exposure on electrocorticogram of rats. Neurotoxicology 1996 Fall-Winter;17(3-4):719-23.
  19. Bucio L, Garcia C, Souza V, Hernandez E, Gonzalez C, Betancourt M, Gutierrez-Ruiz MC Uptake, cellular distribution and DNA damage produced by mercuric chloride. Mutat Res 1999 Jan 25;423(1-2):65-72.
  20. Hua MS, Huang CC, Yang YJ Chronic elemental mercury intoxication: neuropsychological follow-up case study. Brain Inj 1996 May;10(5):377-84.
  21. Grandjean P, Weihe P, White RF, Debes F Cognitive performance of children prenatally exposed to "safe" levels of methylmercury. Environ Res 1998 May;77(2):165-72.
  22. Hock C, Drasch G, Golombowski S, Muller-Spahn F, Willershausen-Zonnchen B, Schwarz P, Hock U, Growdon JH, Nitsch RM Increased blood mercury levels in patients with Alzheimer's disease. J Neural Transm 1998;105(1):59-68.
  23. Oskarsson A, Palminger Hallen I & Sundberg J. Exposure to toxic elements via breast milk. Analyst 120(3):765-770 (1995).
  24. Hock C, Drasch G, Golombowski S, Muller-Spahn F, Willershausen-Zonnchen B, Schwarz P, Hock U, Growdon JH, Nitsch RM Increased blood mercury levels in patients with Alzheimer's disease. J Neural Transm 1998;105(1):59-68.
  25. Wenstrup D, Ehmann WD, Markesbery WR Trace element imbalances in isolated subcellular fractions of Alzheimer's disease brains. Brain Res 1990 Nov 12;533(1):125-31
  26. Basun H, Forssell LG, Wetterberg L, Winblad B Metals and trace elements in plasma and cerebrospinal fluid in normal aging and Alzheimer's disease. J Neural Transm Park Dis Dement Sect 1991;3(4):231-58.
  27. Hock C, Drasch G, Golombowski S, Muller-Spahn F, Willershausen-Zonnchen B, Schwarz P, Hock U, Growdon JH, Nitsch RM Increased blood mercury levels in patients with Alzheimer's disease. J Neural Transm 1998;105(1):59-68.
  28. Pendergrass JC, Haley BE, Vimy MJ, Winfield SA, Lorscheider FL Mercury vapor inhalation inhibits binding of GTP to tubulin in rat brain: similarity to a molecular lesion in Alzheimer diseased brain. Neurotoxicology 1997;18(2):315-24.
  29. Opitz H, Schweinsberg F, Grossmann T, Wendt-Gallitelli MF, Meyermann R Demonstration of mercury in the human brain and other organs 17 years after metallic mercury exposure. Clin Neuropathol 1996 May-Jun;15(3):139-44.
  30. Sanfeliu C, Sebastia J, Cristofol R, Rodriguez-Farre E. Neurotoxicity of organomercurial compounds. Neurotox Res. 2003;5(4):283-305.
  31. el-Fawal HA, Gong Z, Little AR, Evans HL Exposure to methylmercury results in serum autoantibodies to neurotypic and gliotypic proteins.Neurotoxicology 1996 Summer;17(2):531-9.
  32. Faustman EM, Ponce RA, Ou YC, Mendoza MA, Lewandowski T, Kavanagh T. Investigations of methylmercury-induced alterations in neurogenesis. Environ Health Perspect. 2002 Oct;110 Suppl 5:859-64.
  33. Reading R. Thimerosal and the occurrence of autism: negative ecological evidence from Danish population-based data. Child Care Health Dev. 2004 Jan;30(1):90-1.
  34. Qvarnstrom J, Lambertsson L, Havarinasab S, Hultman P, Frech W. Determination of methylmercury, ethylmercury, and inorganic mercury in mouse tissues, following administration of thimerosal, by species-specific isotope dilution GC-inductively coupled plasma-MS. Anal Chem. 2003 Aug 15;75(16):4120-4.
  35. Shanker G, Syversen T, Aschner M. Astrocyte-mediated methylmercury neurotoxicity. Biol Trace Elem Res. 2003 Oct;95(1):1-10.
  36. Zheng W, Aschner M, Ghersi-Egea JF. Brain barrier systems: a new frontier in metal neurotoxicological research. Toxicol Appl Pharmacol. 2003 Oct 1;192(1):1-11.
  37. Kawase T, Ishikawa I, Orikasa M, Suzuki A. An assessment of the impact of thimerosal on childhood neurodevelopmental disorders. Geier DA, Geier MR. J Biochem (Tokyo). 1989 Jul; 106(1): 8-10. Aluminum enhances the stimulatory effect of NaF on prostaglandin E2 synthesis in a clonal osteoblast-like cell line, MOB 3-4, in vitro. Pediatr Rehabil. 2003 Apr-Jun;6(2):97-102.
  38. Geier MR, Geier DA. Thimerosal in childhood vaccines, neurodevelopmental disorders, and heart disease in the United States. J Amer Physc Surg 8: 6-11, 2003.
  39. Allen JW, Shanker G, Tan KH, Aschner M. The consequences of methylmercury exposure on interactive functions between astrocytes and neurons. Neurotoxicology 23: 755-759, 2002.
  40. Hansen JC, Reske-Nielsen E, et al. Distribution of dietary mercury in a dog. Quantitation and localization of total mercury in organs and central nervous system. Sci Total Environ 78: 23-43, 1989.
  41. Zanoli P, Cannazza G, Baraldi M. Prenatal exposure to methyl mercury in rats: focus on changes in kyrenine pathway. Brain Res Bull 55: 235-238, 2001.
  42. Olivieri G, Brack C, et al. Mercury induces cell cytotoxicity and oxidative stress and increases beta-amyloid secretion and tau phosphorylation in SHY5Y neuroblastoma cells. J Neurochem 74: 231-236, 2000.
  43. Juarez BI, Mattinez M, et al. Methylmercury increases glutamate extracellular levels in frontal cortex of awake rats. Neurotoxicology and Teratology 24: 767-771, 2002.
  44. Geier DA, Geier MR. An assessment of the impact of thimerosal on childhood neurodevelopmental disorders. Pediatric Rehabil 6: 97-102, 2003.
  45. Geier DA, Geier MR. A comparative evaluation of the effects of MMR immunization and mercury doses from thimerosal-containing childhood vaccines on the population prevalence of autism. Med Sci Monit 10: P133-139, 2004.
  46. Baskin DS, Ngo H, Didenko VV. Thimerosal indices DNA breaks, caspase-3 activation, membrane damage, and cell death in cultured human neurons and fibroblast. Toxicol Sci 74: 361-368, 2003.
  47. Pichichero ME, et al. Mercury concentrations and metabolism in infants receiving vaccines containing thimerosal: a descriptive study. Lancet 360: 1737-1741, 2002.
  48. Murata K, Dakeishi M. Impact of prenatal methylmercury exposure on child neurodevelopment in the Faroe Islands. Nippon Eiseigaku Zasshi 57: 564-570, 2002.
  49. Davidson PW, Myers GJ, et al (Clarkson TW-member of panel) Effects of prenatal and postnatal exposure from fish consumption on neurodevelopment: outcomes at 66 months of age in the Seychelles Child Development Study. JAMA 280: 701-707, 1998.
  50. Palumbo DR, Cox C, et al. (ClarksonTW) Association between prenatal exposure to methylmercury and cognitive functioning in Seychellois children: a reanalysis of the McCarthy Scales of Children's Ability from the main cohort study. Environ Res 84: 81-88, 2000.
  51. Hornig M, Chian D, Lipkin WI. Neurotoxic effects of postnatal thimerosal are mouse strain dependent. Mol Psychiatry (In press).
  52. Ueha-Ishibashi T, et al. Property of thimerosal-induced decrease in cellular content of gluatathione in rat thymocytes: a flow cytometric study with 5-chloromethylfluorescein. Toxicol in Vitro 18: 563-569, 2004.
  53. Ueha-Ishibaschi T, et al. Effect of thimerosal, a preservative in vaccines, on intracellular Ca+2 concentration of ra cerebellar neurons. Toxicology 195: 77-84, 2004.
  54. Havarinasab S, Lambertsson L, et al. Dose-response study of thimerosal-induced murine systemic autoimmunity. Toxicol Appl Pharmacol 194: 169-179, 2004.
  55. Verstraeten T, Davis RL, DeStefano F, et al. Safety of thimerosal-containing vaccines: a two-phase study of computerized health maintenance organization databases. Pediatrics 112: 1039-1048, 2003. (This is the published study that was discussed in the conference. Here the damaging data is erased and the public is told the thimerosal-containing vaccines are perfectly safe. In this paper Dr. Verstraeten identified himself as working for the CDC, but in fact he is working for GlaxoSmithKline. The editors of the journal Pediatrics should have been willing to disclose this information once it was brought to their attention but they would not.).
Aluminum References
  1. Murayama H, Shin RW, Higuchi J, Shibuya S, Muramoto T, Kitamoto T. Interaction of aluminum with PHFtau in Alzheimer's disease neurofibrillary degeneration evidenced by desferrioxamine-assisted chelating autoclave method.Am J Pathol. 1999 Sep;155(3):877-85.
  2. Shin RW, Kruck TP, Murayama H, Kitamoto T. A novel trivalent cation chelator Feralex dissociates binding of aluminum and iron associated with hyperphosphorylated tau of Alzheimer's disease. Brain Res. 2003 Jan 24;961(1):139-46.
  3. Li W, Ma KK, Sun W, Paudel HK. Phosphorylation sensitizes microtubule-associated protein tau to Al(3+)-induced aggregation. Neurochem Res. 1998 Dec;23(12):1467-76.
  4. Singer SM, Chambers CB, Newfry GA, Norlund MA, Muma NA. Tau in aluminum-induced neurofibrillary tangles. Neurotoxicology. 1997;18(1):63-76.
  5. Toda S, Yase Y. Effect of aluminum on iron-induced lipid peroxidation and protein oxidative modification of mouse brain homogenate. Biol Trace Elem Res. 1998 Feb;61(2):207-17.
  6. Sayre LM, Perry G, Harris PL, Liu Y, Schubert KA, Smith MA. In situ oxidative catalysis by neurofibrillary tangles and senile plaques in Alzheimer's disease: a central role for bound transition metals. J Neurochem. 2000 Jan;74(1):270-9.
  7. Xie CX, Yokel RA. Aluminum facilitation of iron-mediated lipid peroxidation is dependent on substrate, pH and aluminum and iron concentrations. Arch Biochem Biophys. 1996 Mar 15;327(2):222-6.
  8. Kawase T, Ishikawa I, Orikasa M, Suzuki A. Aluminum enhances the stimulatory effect of NaF on prostaglandin E2 synthesis in a clonal osteoblast-like cell line, MOB 3-4, in vitro. J Biochem (Tokyo). 1989 Jul; 106(1): 8-10.
  9. Jope RS. Modulation of phosphoinositide hydrolysis by NaF and aluminum in rat cortical slices. J Neurochem. 1988 Dec; 51(6): 1731-6.
  10. Blair HC, Finch JL, Avioli R, Crouch EC, Slatopolsky E, Teitelbaum SL. Micromolar aluminum levels reduce 3H-thymidine incorporation by cell line UMR 106-01. Kidney Int. 1989 May; 35(5): 1119-25.
  11. Shainkin-Kestenbaum R, Adler AJ, Berlyne GM, Caruso C. Effect of aluminium on superoxide dismutase. Clin Sci (Lond). 1989 Nov; 77(5): 463-6.
  12. Kawase T, Orikasa M, Suzuki A. Aluminofluoride- and epidermal growth factor-stimulated DNA synthesis in MOB 3-4-F2 cells. Pharmacol Toxicol. 1991 Nov; 69(5): 330-7.
  13. Gomes MG, Moreira CA, Mill JG, Massaroni L, Oliveira EM, Stefanon I, Vassallo DV. Effects of aluminum on the mechanical and electrical activity of the Langendorff-perfused rat heart. Braz J Med Biol Res. 1994 Jan; 27(1): 95-100.
  14. Jope RS. Modulation of phosphoinositide hydrolysis by NaF and aluminum in rat cortical slices. J Neurochem. 1988 Dec; 51(6): 1731-6.
  15. Husaini Y, Rai LC, Mallick N. Impact of aluminium, fluoride and fluoroaluminate complex on ATPase activity of Nostoc linckia and Chlorella vulgaris. Biometals. 1996 Jul; 9(3): 277-83.
  16. Blair HC, Finch JL, Avioli R, Crouch EC, Slatopolsky E, Teitelbaum SL. Micromolar aluminum levels reduce 3H-thymidine incorporation by cell line UMR 106-01. Kidney Int. 1989 May; 35(5): 1119-25.
  17. Lai JC, Lim L, Davison AN. Effects of Cd2+, Mn2+, and Al3+ on rat brain synaptosomal uptake of noradrenaline and serotonin. J Inorg Biochem. 1982 Nov; 17(3): 215-25.
  18. Shainkin-Kestenbaum R, Adler AJ, Berlyne GM, Caruso C. Effect of aluminium on superoxide dismutase. Clin Sci (Lond). 1989 Nov; 77(5): 463-6.
  19. Department of Health and Human Services National Vaccine Program Office Presents: Workshop on Aluminum in Vaccines. Caribe Hilton International Hotel, San Juan, Puerto Rico: Jointly sponsored by: task Force for Child Survival and Development. May 12, 200.
  20. Varner JA, Jenson KF, Harvath W, Isaacson RL. Chronic administration of aliminum-fluoride or sodium-fluoride to rats in drinking water: alterations in neuronal and cerebrovascular integrity. Brain Res 784: 284-298, 1998.
  21. Strunecka A, Pataocka J. Aluminofluoride complexes: new phosphate analogues for laboratory investigations and potential danger for living organisms.
    http://www.fluoridation.com/brain3.htm
  22. Candura SM, Castildi AF, et al. Interaction of aluminum ions with phosphoinositide metabolism in rat cerebral cortical membranes. Life Sci 49: 1245-1252, 1991.
  23. Publicover SJ. Brief exposure to the G-protein activator NaF/ AlCl3 induces prolonged enhancement of synaptic transmission in area of rat hippocampal slices. Expl Brain Res 84: 680-684, 1991.
  24. Brenner A. Macrophagic myofascitiitis: a summery of Dr. Gherardi's presentations. Vaccine 20Supp 3): S5-6, 2002.
  25. Lacson AG, D'Cruz CA, et al. Aluminum phagocytosis in quadriceps muscle following vaccination in children: relationship to macrophagic myofasciitis. Pediatr Dev Pathol 5: 151-158, 2002.
  26. Flarend RE, Hem SL, et al. In vivo absorption of aluminum-containing vaccine adjuvants using 26 Al. Vaccine 15: 131401318, 1997.
  27. Authier FJ Cherin P, et al. Central nervous system disease in patients with macrophagic myofasciitis. Brain 124: 974-983, 2001.
  28. Gherardi RK. Lessons from macrophagic myofasciitis: towards definition of a vaccine adjuvant-related syndrome. Rev Neurol (Paris) 159: 162-164, 2003.
  29. Bergfors E, Trollfors B, Inerot A. Unexpectantly high incidence of persistent itching and delayed hypersensitivity to aluminum in children after the used of absorbed vaccines from a single manufacturer. Vaccine 22: 64-69, 2003.
  30. Deloncle R, Fauconneau B, et al. Aluminum L-glutamate complexes in rat brain cortex: in vivo prevention of aluminum deposit by magnesium D-aspartate. Brain Res 946: 247-252, 2002.
  31. Mundy WR, Freudenrich TM, Kodavanti PR. Aluminum potentates glutamate-induced calcium accumulation and iron-induced oxygen free radical formation in primary neuronal cultures. Mol Chem Neuropathol 32: 41-57, 1997.
References Concerning Lead
  1. Naatala JT, Loikkanen JJ, et al. Lead amplifies glutamate-induced oxidative stress. Free Radical Biology Medicine 19: 689-693, 1995.
  2. Morgan RE, Garavan H, et al. Early lead exposure produces lasting changes in sustained attention, response initiation, and reactivity to errors. Neurotoxicology and Teratology 23: 519-531, 2001.
  3. Needleman HL, McFarland C, et al. Bone lead levels in adjudicated delinquents: A case control study. Neurotoxicology and Teratology 24: 711-717, 2002.
  4. Dietrich KN, Ris MD, et al. Early exposure to lead and juvenile delinquency. Neurotoxicology and Teratology 23: 511-518, 2001.
My References
  1. Blaylock R. Interaction of cytokines, excitotoxins, and reactive nitrogen and oxygen species in autism spectrum disorders. J. Amer Nutr Assoc 6: 21-35, 2003.
  2. Blaylock RL. The central role of excitotoxicity in autism spectrum disorders. J Amer Nutra Assoc 6: 7-19, 2003.
  3. Blaylock RL. Chronic microglial activation and excitotoxicity secondary to excessive immune stimulation: possible factors in Gulf War Syndrome and autism. J Amer Phys Surg 9: 46-51, 2004.

Other Unreasonable Happiness Posts You Would Be Interested In

Get Better Now!... Living Mastery
Show Archives:




Did you find this information useful?
Then pay it forward. Help my Scholarship Students with their tuition and allow me to create more of my Free Programs and Shows for everyone. How? Just click below to Donate, any amount is greatly appreciated and it all goes to a good cause.






Thank You,
Sifu Marcus Lovemore

Translate

My Most Popular Posts