Why Millennials Might be Different from Other Generations

Millennials / Generation Y

Millennials, or Generation Y, are referred to as the “Snowflake Generation”. They were born between about 1982-2000. They are currently, as of 2019, between approximately 19 and 39 years of age. They follow Generation X and precede Generation Z.

Snowflakes and Triggered

A “snowflake” is a person who is considered to be overly sensitive or too easily offended. Millennials get “triggered”. According to the Slang Dictionary, the word “triggered” is used to describe someone who is angry and filled with hate. A person usually gets triggered after seeing something upsetting. Using the expression “triggered” is way to describe irritable people.

Characteristics of Millennials

According to a 2013 article in Time magazine by Joel Stein and david york’s tax service and preparation site, Millennials have characteristics that are different from other generations. Stein states that millennials lack the kind of empathy that allows them to feel concerned for others, but they even intellectually understanding others’ points of view. According to Stein, Millennials are interacting all day but almost entirely through a screen. They are most often sitting next to one another and texting. They might look calm, he further describes, but they’re deeply anxious.

Loneliness is also something that greatly troubles Millennials. They tend to rely on technology to stay in communication with others.

Interestingly, they are also reported to have declining fertility. In addition, they are more likely to be diagnosed with mental illnesses such as depression, schizophrenia, or bipolar disorder.

Millennials are Social Justice Warriors

Millennials are also the generation of “Social Justice Warriors”. A recent (2019) “Democratic Socialist Convention”, filled with Millennials, made the news when the convention speakers were frequently interrupted by Millennials complaining about “sensory overload” and being “triggered”. Clapping was not allowed because clapping was “triggering”. Quiet spaces were available and the use any scents/fragrances was discouraged.

Millennials are different

So why are Millennials different? Most explanations include growing up with technology. But Generation Z also grew up with technology. Other explanations include parenting. But are parents from Generation X and Z that different from parents of Generation Y (Millennials)?

As a Neurotoxicologist, I have my own theory. If you look at the Table below you will see the differences in mercury exposure levels from childhood vaccines between the generations. The Millennials received 3 to 9 times the amount of mercury of previous generations, and up to 237 times the following generation, Generation Z.


Generation Year of Birth Mercury Exposure from Childhood Vaccines (micrograms)
Veterans 1922-45 25-50
Baby Boomers 1946-64 25-75
Generation X 1965-81 25-75
Generation Y


1982-2000 150-237
Generation Z 2001- present 0

Table 1: Differences in the amount of mercury exposure from childhood vaccines between the generations.

thimerosal and autism timeline

Millennials and Mercury 

Moreover, the characteristics associated with Millennials are also associated with mercury exposure, i.e., lack of empathy, problems with “Theory of Mind” (or understanding others), anxiety, sensory sensitivity, social phobia, being socially withdrawn, depression, irritability, infertility, and difficulty controlling anger. Basically, Millennials were exposed to much higher levels of mercury than are considered safe by the EPA through no fault of their own.

Who is at fault? Probably the FDA, which was admittedly, “asleep at the wheel” and not paying attention to the amount of mercury these children were given. The good news is that mercury was taken out of childhood vaccines in the US in about 2002. The bad news is that this generation is going to also be more susceptible to dementia later in life.

Call them Millennials or Snowflakes, but, in reality, evidence suggests many of them are basically on the Spectrum as a result of mercury exposure in infancy.

Mercury Science Vaccines

Mercury in Vaccines – 10 Lies About The Safety of Thimerosal

Mercury in Vaccines – 10 Lies About the Safety of Thimerosal

Refuted by a Mother who Knows Better

by Rev. Lisa K. Sykes

Lie # 1 “Thimerosal, 49.55% mercury by weight, is safe when used as a preservative in vaccines and other drugs.”

Mercury in vaccinesThe Facts: The Eli Lilly Material Safety Data Sheet (MSDS) for Thimerosal acknowledges that exposure to Thimerosal in utero and in children can cause “mild to severe mental retardation and mild to severe gross motor impairment.” The Sigma Aldrich MSDS lists abortion and fetal death as possible outcomes of in utero exposure.

Nonetheless, most seasonal and H1N1 flu shots for pregnant women and young children contain 25 micrograms of mercury in the form of Thimerosal. For this exposure to be safe, a child would need to weigh more than 550 pounds.

Thimerosal is a poison, neurotoxin, cancer-causer, and can interrupt the immune system and the normal development of an unborn baby or a child. Thimerosal is so toxic that putting it on your skin is illegal. However, the government not only allows but also defends its injection into the population, especially pregnant women and newborn children, as part of influenza vaccines currently recommended by the US Centers for Disease Control and Prevention (CDC).

Lie #2 “Mercury was removed from all childhood vaccines in (pick any year between 1999 and the present).”

The Facts: After “realizing” the amount of mercury in the childhood vaccination schedule recommended by the CDC exceeded all national and global maximum safety limits, the American Academy of Pediatrics and the United States Public Health Service called for the immediate removal of Thimerosal from all vaccines on July 7, 1999.

By 2003, the vaccine manufacturers had begun to react to the 1999 call by lowering the mercury content in many of the Thimerosal-preserved early childhood vaccines. However, in April of 2002, the CDC began recommending that pregnant women and very young children get annual Thimerosal-preserved flu shots. The result was a ‘shell game’ which has caused widespread confusion in the public because of press reports declaring, “Since (select a year between 1999 and the present), mercury has been removed from all recommended vaccines for children except for some flu shots.” Get info about it on

Astoundingly, the total level of mercury exposure, if a child receives all the possible CDC-recommended vaccinations that are still Thimerosal preserved, from 6 months to 18 years of age, has actually increased. Significantly, if you put the amount of mercury added to the immunization schedule as a result of the CDC-recommended seasonal and (in 2009) H1N1 flu shots** on one side of a scale, and the amount of mercury that was subtracted from that schedule by reformulating early childhood vaccines without Thimerosal on the other side, the total amount of mercury added far outweighs the amount of mercury subtracted. In addition, today most tetanus shots and the multi-dose Sanofi Menomune® vaccine that are approved by the US Food and Drug Administration (FDA) still contain 25-micrograms-a-dose mercury.

Currently, the actions taken by the vaccine manufacturers, the FDA and the CDC have increased the possible maximum childhood exposure to mercury from vaccines to twice the level that triggered the 1999 call to remove mercury from all vaccines as soon as possible! Also, new vaccine formulations with 25 micrograms of mercury per 0.5-mL dose are still being approved by the FDA for administration to pregnant women and children.

**Most doses of these flu vaccines are Thimerosal-preserved.

Lie #3 “Thimerosal is well-tested, having been used for 70 years with no problems.”

The Facts: Thimerosal has never undergone even one modern safety test. It was developed in 1927 and patented by Eli Lilly in 1928. It was first tested on small animals and killed a variety of mice, rabbits and chicks. After the animals died from exposure to Thimerosal, the decision was made to administer it to 22 patients suffering from bacterial meningitis during an epidemic in Indianapolis, Indiana in 1929.

Of the 22 persons given Thimerosal, all died, most within a day or two of administration. The doctor overseeing the trial, on stipend from Eli Lilly, declared that the patients had all died of meningitis and that Thimerosal was not observed to have caused any problem when administered to his patients. With that declaration, and a subsequent one by Eli Lilly staff that Thimerosal has a low order of toxicity for man, even though it killed small animals, Thimerosal was introduced into the drug supply. Yet, despite warnings in the published scientific literature that Thimerosal was toxic, and despite opposition to its use in every decade since, Thimerosal has remained in the drug supply.

The first protest on record against this highly toxic mercury compound was made in 1935 by the Pittman Moore Company which declared that, after testing, it found Thimerosal “was unsuitable as a preservative in serum intended for use in dogs…”

The FDA, passive with regard to safety testing, has never provided the results of appropriate toxicological tests on Thimerosal. Factually, the vaccine makers who use Thimerosal as a preservative are required by law to conduct and submit the results of such safety tests to the FDA before the FDA can legally approve a vaccine with how to succeed online. Yet, the FDA has yet to produce even one of these vaccine maker’s toxicity studies, demonstrating Thimerosal safe for administration to humans, despite the fact that these documents have been sought in a court of law.

Lie #4 “No published peer-reviewed studies have shown any harm from Thimerosal.”

The Facts: The published scientific literature about Thimerosal can be divided into two distinct sets with opposite conclusions regarding its toxicity.

The first set is comprised of studies directly or indirectly supported by the pharmaceutical industry, showing that “there is no evidence of harm” from Thimerosal. These studies are the ones most often quoted by the Press. Most of these studies are statistical. In many cases, the data from which their conclusions are derived have been ‘lost’ or are unavailable or inconsistent. Significantly, the 2004 Institute of Medicine Vaccine Safety Review Committee, which defended Thimerosal, relied upon such statistical studies rather than the clinical evidence that the committee received.

The second set is comprised of hundreds of independent clinical and statistical studies demonstrating harm from Thimerosal. These studies are seldom quoted by the Press. Authors of these scientific papers include chemists, biologists, physicians and neurologists among others. Federal grants have often funded these studies. However, in many instances, when a researcher has concluded that Thimerosal causes harm, the grant has been withdrawn or ended. In one case, this happened after a researcher found an “autistic-like” condition in developing mice given injected mercury exposures like those human babies received from the CDC’s 1990’s immunization schedule. Independent researchers have lost jobs, been ostracized by peers, and/or had their medical licenses threatened, all because they dared to declare Thimerosal dangerous.

Published studies have shown that Thimerosal and its mercury breakdown product contribute to: Alzheimer’s, Cancer, Autism Spectrum Disorders, Attention Deficit Disorders, Bipolar Disorder, Asthma, Sudden Infant Death Syndrome, Arthritis, Food Allergies, Premature Puberty, and Infertility.

Offered for your consideration:

Watch the University of Calgary Video Showing Effects of Mercury on Neurons
[velocity type=”youtube” options=”rel=0&showinfo=0″ id=”pPVxiDpsNDg” img=”” alt=”Mercury destroying brain neurons” color=”#000000″ bkg_color=”transparent”]

Lie #5 “No federal statements indicate any cause for concern regarding the continuing use of Thimerosal.”

The Facts: The following critical federal statements testify to the likelihood of egregious conflict of interest and possible collusive activity with regard to the acceptance of Thimerosal by manufacturers, the FDA and the CDC:

After a three-year investigation, a Congressional report released May 2003 by the staff of the Subcommittee on Human Rights and Wellness, Committee on Government Reform, “Mercury in Medicine” Hearings of the United States House of Representatives stated:

“Thimerosal used as a preservative in vaccines is likely related to the autism epidemic. This epidemic in all probability may have been prevented or curtailed had the FDA not been asleep at the switch regarding the lack of safety data regarding injected thimerosal and the sharp rise of infant exposure to this known neurotoxin. Our public health agencies’ failure to act is indicative of institutional malfeasance for self-protection and misplaced protectionism of the pharmaceutical industry.”

On May 22, 2004, after hundreds of disclosures from citizens to the Office of Special Counsel, US Special Counsel Scott Bloch issued this statement:

“I hasten to add, however, that based on the publicly available information…it appears there may be sufficient evidence to find a substantial likelihood of a substantial and specific danger to the public health caused by the use of thimerosal/mercury in vaccines because of its inherent toxicity.”

On July 15, 2005, Liz Birt, J.D., L.L.M., (former legal counsel to the Government Reform Committee, US House of Representatives) and Jim Moody, J.D., in a letter to Lauren Fuller, Chief Investigative Counsel, United States Senate Health, Education, Labor, and Pensions (H.E.L.P.) Committee outlined a “Thimerosal Timeline” and a “Statement of Criminal Charges” against specific Federal Officials, including the following:

“FDA: Criminal negligence in not instituting a Class I recall of all vaccines administered to infants containing Thimerosal in July of 1999 and again in June of 2000…”

On July 19, 2004, Michael E. Little, Deputy Inspector General for Investigations in the Office of the Inspector General for the Department of Health and Human Services, in a letter to Rev. Lisa K. Sykes, stated:

“…we have determined that your above allegation (that Thimerosal is being used in order to increase the manufacturer’s profit margins) represents a potential conflict-of-interest issue which may be criminal in nature…”

Lie #6 “Individuals who oppose the use of mercury in medicine are anti-vaccine.”

The Facts: Contrary to sound bites you hear on the nightly news, to be “anti-mercury” is not to be “anti-vaccine.” In fact, by advocating this common-sense measure of removing mercury to ensure the safety of vaccines, anti-mercury advocates are actually championing vaccine safety. The Vaccine Program of this nation should not be a delivery system for a poison. Those arguing against the unnecessary use of a known neurotoxin in the vaccine/drug supply are seeking to safeguard public confidence in the vaccine program, not destroy it. Anti-mercury advocates want vaccines to be produced with non-toxic preservatives or, better yet, with no preservatives using clean manufacturing processes, a realistic and viable option in developed nations since the 1980s.

Tragically, in the face of catastrophic liability, those who defend mercury as a part of medicine are failing to correct a grave mistake. This mistake is a clear and present danger to the public and, especially, to the children. Inertia and denial in the federal government and in industry are contributing to the medical community’s protecting the place of mercury in medicine rather than protecting the health and safety of patients. This ordering of priorities is unethical.

If left uncorrected, this situation will continue to destroy public confidence in our national vaccine programs as more and more people realize that the escalating rates of chronic illness and developmental disorders are associated with Thimerosal, an unnecessary and indefensible part of our vaccines. Importantly, we are not assessing what the injuries already caused by Thimerosal will do to our nation’s future productivity with the government-admitted rate of 1-in-every-6 children being diagnosed with a developmental or behavioral disorder in 2004. Advocates calling for the removal and ban of the use of mercury are seeking to avoid an impending public health crisis by assuring that, immediately, vaccines are: a) made safer and b) manufactured according to all the current applicable federal safety regulations — not the non-existent drug safety laws of 1929!

Lie #7 “The movement to ban mercury from medicine is comprised of ‘hysterical’ parents who wrongly blame vaccines for their children’s autism.”

The Facts: Parents of mercury-injured children continue to argue tirelessly that unnecessarily exposing a child, in utero or after birth to mercury, is an avoidable risk. They know this avoidable risk is logically associated with the onset of neurodevelopmental and other disorders. With no compelling reason to use an ineffective neurotoxin as a preservative, and every reason, based on Thimerosal’s demonstrated toxicity, to eliminate it, parents make a logical, reasoned argument for banning Thimerosal from medicine –especially from vaccines intended for our children whose brains are still developing.

A growing number of informed physicians, politicians, and independent scientists are joining in this no-nonsense argument for placing the well-being of children first, above the profit margins of manufacturers. These professionals and, now, the faith community have joined in the call for “Protecting Children from Mercury-containing Drugs.”

On April 29, 2008, the General Conference of the United Methodist Church, representing 11.5-million persons of the Christian Faith, adopted a statement of the same name as a global and historic resolution of the denomination. This resolution calls upon the World Health Organization, international and national health officials/agencies, including the US Secretary of Health and Human Services, the FDA and the CDC to:

* immediately prioritize mercury-free stocks of vaccines and other pharmaceutical products for pregnant women, newborn infants and children;

* provide “the opportunity of informed consent” and promote product education to individuals about mercury exposure through their pharmaceutical products or vaccines, detailing the known risks of toxicity and Federal Safety Guidelines for exposure to mercury; and

And it further resolves, that:

“until mercury is banned from medicine, the medical missions, hospitals, clinics and ministries of The United Methodist Church strongly encourage use of mercury-free vaccines over mercury-containing ones. Acknowledging the difficulties in some contexts, we strongly urge that other organizations who are responsible for immunization efforts to prevent disease such as the Global Alliance for Vaccines and Immunizations, United Nations Children’s Fund (UNICEF), Rotary International, the Bill and Melinda Gates Foundation, as well as any other organization from which vaccines are purchased, join The United Methodist Church in the educating the public about and advocating for mercury-free drugs and vaccines.”

With this bold witness by the United Methodist Church, the attempt by parent-advocates and others to ban mercury from medicine has appropriately grown into a social justice movement. It is now the community of faith, which esteems each life a priceless gift from God, which will lead this urgent public health reform.

Lie #8 “Autism is genetic.”

The Facts: Billions of dollars are being spent trying to prove that the autism epidemic is genetic. “Genetic drift,” the amount genes change over time, is 1% per 100 years. Therefore, with such a slow pace of change, there can be no such thing as a sudden ‘genetic epidemic.’ While a rare type of genetic autism may exist (at the background rate of ‘1 in 10,000’), the autism epidemic (at about ‘1 in 100’) cannot be due to genetic drift.

In addition, if autism were genetic, because it affects more males than females, geneticists teach us that it would have to be to an X-chromosome-linked disorder. (Girls, having two X chromosomes, would then have a redundant good chromosome, so the disorder would not manifest as often in females as in males who have only one X chromosome.) For a girl to have autism then, she would need to receive a defective X-chromosome from each parent, meaning they both carried the defect. The problem lies in the fact that if the father has the defect to pass onto his daughter, and it is on his only X-chromosome, then he should be affected by the disorder as well. Since autistic daughters rarely, if ever, have autistic fathers, the theory that “autism is genetic” fails because its claim does not match the empirical evidence.

There are two main recognized causes for any epidemic: an infectious agent or a widespread toxic exposure. Autism is due to the latter. Corresponding to the sharply increasing level of mercury in the immunization schedule globally, which started in the late 1980’s, there has been an increasing rate of autism among children. This also explains why autism among 40-, 50-, 60-, 70- and 80-year-olds is not epidemic, but rather rare. Those over 30 did not routinely get levels of vaccine-related mercury exposure high enough to cause autism.

Only when autism is understood as a widespread toxic exposure, can you explain the fact that everywhere boys are affected about 4 times more often with this disorder than girls. Researchers have established that testosterone increases the toxicity of mercury, while estrogen protects from it. Therefore, at the level contained in our vaccines, mercury affects boys disproportionately due to their having higher testosterone levels. This is what creates the ‘4 to 1’ ratio of males to females affected by the level of mercury poisoning in our children that is labeled as autism.

While there are many contributing and lesser sources of environmental mercury exposure, the one which precipitously and simultaneously changed with the advent of the autism epidemic was the mercury exposure from the increasing number of Thimerosal-preserved vaccines in the CDC’s recommended childhood vaccination schedules. Those children with a higher sensitivity to mercury and/or a higher level of exposure are those most impacted by this increased exposure to vaccine mercury. This is why not all children who received mercury-preserved vaccines are autistic: while the autism epidemic is not genetic, susceptibility to mercury poisoning has a strong genetic component and is unique for each individual!

Lie #9 “Since mercury was removed from vaccines, autism has increased, so Thimerosal cannot be the cause of the autism epidemic.”

In the face of such a statement, one must ask whether the mercury has truly been removed from vaccines in the country referenced. Then, one must ask from what year the sample rates under discussion were taken. The current rate given in the American media is about ‘1 in 100’. This rate is based upon statistics from children born in 1998. In regard to this particular rate and year, it reflects a time when mercury had not been removed in the United States, and the ‘1 in 100’ rate is actually not a new measure, but rather a crude estimate from among the peak years of mercury exposure in the American early childhood immunization schedule.

In assessing more current rates of autism, computed based on data from 2002 on, remember that while mercury was removed from many early childhood vaccines, it was reintroduced at the preservative level into the childhood schedule in the form of the seasonal and, later, the H1N1 flu vaccines. With each passing year since, more flu shots have been recommended, and the categories of persons who should take them, based on health conditions and age, have been expanded. So, continuing diagnosis rates for autism and other chronic illnesses simply reflect the continuing presence of mercury in the current vaccine supply to the present day.

Some foreign studies which claim that the autism rate increased after Thimerosal was removed are equally misleading. From Denmark, for example, a study actually began by counting only children with autism who were institutionalized.

Then when the government announced the Thimerosal had been removed from vaccines, suddenly home-bound children with autism were added to the count. Therefore, the number of children diagnosed with autism in the study did rise ‘once the mercury was removed’ – not because more children were diagnosed but only because more with diagnoses were counted! Studies such as these are known as “Garbage in-Garbage out” studies. When the basis of a study changes in the middle and this fact is omitted from its publicized results, then the perception created by the study is false.

What we do know is that the factual and complete removal of mercury from the vaccine/drug supply would tell us, definitively, if mercury caused the autism epidemic. Sadly, such attempts to completely withdraw Thimerosal have met with loud objections from the American Academy of Pediatrics, the American Medical Association, the Institute of Medicine of the United States National Academy of Sciences, and others. These organizations, as well as our national health agencies, have actually lobbied federal and state officials to keep Thimerosal in vaccines.

Among the Amish who do not vaccinate, the rate of autism is strikingly low. Among those Pennsylvania Amish children actually diagnosed with autism, three were adopted and had received their vaccines prior to adoption, and one lived down-wind of a coal-burning power plant. Such anecdotal evidence suggests that the increases in recommended mercury-containing vaccines are causally related to the autism epidemic. If ypu are a couple adopting of wanting to adopt a baby visit Adopt Match help save a child life.

Lie #10 “There’s more mercury in a tuna fish sandwich than there is in one mercury-preserved flu shot.”

Remember, the United States Food and Drug Administration warns pregnant women to limit their consumption of fish because its mercury content may harm their unborn child. Sadly, neither the FDA nor the CDC has issued a similar warning about mercury-preserved flu shots. Clearly, the lack of a warning to pregnant women and young children regarding the mercury content of their vaccines makes no scientific sense.

Another scientific fallacy is the suggestion that the type of mercury (ethyl) in Thimerosal is less toxic than the type of mercury (methyl) in fish. This suggestion is not true. Ethyl mercury is actually more toxic to the kidneys, and equally toxic to other parts of the body as methyl mercury. All forms of mercury are highly toxic. When used in a vaccine, the mercury’s toxicity does not magically disappear! In fact, the mercury in a vaccine poses special dangers because it is injected.

Scientists know that eating mercury in food is completely different from injecting it directly into body and blood. This is because the body has defensive mechanisms to limit the absorption of toxins as they move through the digestive system. Just because you consume mercury in a tuna sandwich does not mean that the total mercury content of that meal will end up in your brain.

By contrast, injecting mercury in the form of Thimerosal directly into the body as part of a vaccine bypasses the body’s natural absorption defenses. The mercury enters the blood stream, but does not remain there long. It escapes from the bloodstream very quickly and enters the tissues in the body. The body is not able to defend itself well against injected mercury, and if a genetic susceptibility to mercury exists, the exposed individual may be able to excrete only minimal amounts of the injected mercury toxin.

We must also note that mercury crosses the placental barrier, and a pregnant woman’s body preferentially dumps mercury into her fetus. Thus, the unborn child, being mostly developing brain, sustains huge exposure from injected mercury, in particular, at critical stages of neurological development.

Remember also, that a newborn moderne child excretes very little mercury. Understanding this, you realize that just because a study may report mercury levels are low in the blood, urine and/or feces after exposure to mercury, this does not mean the child has excreted the toxin (as some have implied in poorly done scientific studies.) Instead, it more likely means that the mercury has already sequestered itself in the vital parts of the body.

For anyone, of any age, mercury delivered through injection behind a body’s defenses is a much more significant exposure than mercury ingested with food. A much greater percentage of the toxic exposure will accumulate in the brain, contributing to neurodevelopmental disorders in the young, and dementia (Alzheimer’s) in the elderly. An increased level of mercury in the body has also been associated with aggression and mood disorders.

It is advisable to avoid mercury whenever you can, whether it is present in food, a vaccine or the environment (air, water, etc.). While many substances in our world, such as tuna fish, contain low levels of mercury, most are not classified as hazardous waste. Unused vaccines with a preservative level of Thimerosal, however, are considered hazardous waste because of their high mercury content. If not injected into patients, discarded vials of these mercury-preserved vaccines, therefore, must be disposed of in steel drums, by law. For help with online gaming check out netent casino games

In contrast, a can of tuna fish is not under this same stipulation, and more importantly, if it were, you wouldn’t eat it, would you?

Our #1 Challenge: To Safeguard the Public from Mercury in Medicines

“The high order of toxicity from Thimerosal and its ethylmercury breakdown product has been known and published for decades. Nonetheless, Thimerosal remains in the drug supply, especially in various vaccines manufactured both for the United States and globally. The ubiquitous and largely unchecked place of Thimerosal in pharmaceutical products, therefore, represents a medical crisis in the modern day hughes air co. Reforms in the manufacture and the licensing of vaccines and other drugs, which should have been accomplished proactively, had anyone properly assessed their mercury content, must now be conducted, reactively, under significant systemic stress. With no warning, recall, or ban of mercury in vaccines and other drugs as of yet, the victim of this mandated, unwarranted, and massive mercury exposure is still an unsuspecting public, and most especially its unborn and newborn children”***.

Coalition for Mercury-Free Drugs (CoMed)

The Coalition for Mercury-Free Drugs is a non-profit organization dedicated to ending the use of mercury in drugs. You can also avail cash loans no guarantor needed. We are a group of researchers and scientists who have collectively published over 200 peer-reviewed scientific papers, and over 35 of those specifically about the harm from Thimerosal. You can find write ups of many of our published studies on our website


David A. Geier1, Lisa K. Sykes2, Mark R. Geier3

1 The Institute of Chronic Illnesses, Inc.,
2 CoMeD, Inc.,
3 The Genetic Centers of America, Silver Spring, Maryland, USA

Journal of Toxicology and Environmental Health, Part B, 10:575–596, 2007.
Copyright © Taylor & Francis Group, LLC
ISSN: 1093-7404 print / 1521-6950 online
DOI: 10.1080/10937400701389875

Mercury Science Vaccines

Mercury in Vaccines: There is No Safe Level

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Mercury in Vaccines: There is No Safe Level

mercury in vaccinesThere are a number of substances and chemicals that have proven harmful and pose a threat to the health of people. The Food and Drug Administration (FDA), Centers for Disease Control and Prevention (CDC), public health officials and medical professionals have worked to safeguard individuals by eliminating or removing substances that can cause diseases and/or illness. However, parents and researchers have raised much concern regarding mercury in vaccines and its connection to illnesses.

Although flu shots are promoted as safe and effective at shielding individuals from getting sick, because of the mercury in vaccines, they can present a risk. While the FDA claims that the amount of mercury used is at a safe level, there is no safe level of any toxin. Any level of a substance, chemical or toxin injected into the body can pose a threat in many ways. Scientist David Geier has explored the use of mercury in vaccines and the effects that follow.

The Harmful Effects of Mercury in Vaccines isn’t New

The toxicity of mercury and its threat to human health is nothing new. In fact, many schools and retail stores have removed mercury-containing items such as thermometers and thermostats because the mercury inside these items poses risk. While the predominant source of mercury exposure is from amalgam dental fillings and mercury in vaccines, children are frequently exposed to mercury when it is mishandled or improperly cleaned up.

But it’s not just about mercury being toxic. We must also factor in the fact that everyone has different levels of susceptibility to its effects. Every individual has a different level of tolerance to mercury and will react differently. Yet when given the flu shot, every individual is given the same amount of mercury whether they are a fetus, infant, child, or adult. Therefore, those with stronger mercury defense systems are not likely to react in the same way as those with weaker mercury defense systems. Check locksmith dublin in nerby.

Thimerosal: mercury in vaccines

Thimerosal is a mercury-based compound that is used as preservative used in many different vaccines given to pregnant women, infants, children, and adults worldwide. Vaccine formulations come in multi-dose vials or single-dose vials. Generally, multi-dose vials of vaccine use Thimerosal as a preservative in order to prevent accidental contamination of the vial. According to the CDC, because the amount of mercury in Thimerosal is present in trace amounts, it does not pose a threat to health. The single-dose vials are created without thimerosal since they are intended to be used only once. You can get loans from

For additional information about why there is no safe level of mercury in vaccines, please watch the video above.


Mercury Science Vaccines

Thimerosal childhood vaccines linked to risk of emotional disturbances

Thimerosal exposure and disturbance of emotions specific to childhood and adolescence: A case-control study in the Vaccine Safety Datalink (VSD) database

official research journal of the International Brain Injury Association (IBIA) thimerosal, mercury, vaccinesDavid A. Geier, Janet K. Kern, Kristin G. Homme & Mark R. Geier


Background: This study evaluated Thimerosal-containing childhood vaccines and the risk of a diagnosis called disturbance of emotions specific to childhood and adolescence (ED). Thimerosal is an organic-mercury (Hg)-containing compound used in some vaccines.

Methods: A hypothesis-testing prospective, longitudinal case-control study evaluated Hg exposure from Thimerosal in hepatitis B vaccines administered at specific times within the first 6 months of life and its association with medically diagnosed ED (313.xx) (n = 517) in children born between 1991–2000 in comparison to controls (n = 27 491) in the Vaccine Safety Datalink (VSD) Dublin Painting Pros site database.

Results: Cases diagnosed with ED were significantly more likely than controls to have received increased Hg exposure within the first month of life (odds ratio (OR) = 1.3384), the first 2 months of life (OR = 1.3367) and the first 6 months of life (OR = 2.37). When the data were separated by gender, similar significant adverse effects were observed for males, but not females designer fashion consignments. On a per microgram Hg basis, cases diagnosed with ED were significantly more likely than controls to have received increased exposure within the first 6 months of life (OR = 1.025 per microgram Hg).

Conclusions: The results show a significant relationship between Hg exposure from Thimerosal-containing childhood vaccines and the subsequent risk of an ED diagnosis.

PMID: 28102704

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  1. HiDoctor’98: The New Generation of Medical Software. International Classification of Diseases [Internet]. [cited 20 Feb 2016]. Available from
  2. Wagner M, Kutash K, Duchnowski AJ, Epstein MH, Sumi WC. The children and youth we serve: a national picture of the characteristics of students with emotional disturbances receiving special education.
  3. Journal of Emotional and Behavioral Disorders 2005;13:79–96.[CrossRef], [Web of Science ®], [Google Scholar]
  4. Wagner M, Newman L. Longitudinal transition outcomes of youth with emotional disturbances. Psychiatric Rehabilitation Journal 2012;35:199–208.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  5. Schettler T. Toxic threats to neurologic development of children. Environmental Health Perspectives 2001;109(Suppl 6):813–816.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  6. Kern JK, Haley BE, Geier DA, Sykes LK, King PG, Geier MR. Thimerosal exposure and the role of sulfation chemistry and thiol availability in autism. International Journal of Environmental Research & Public Health 2013;10:3771–3800.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  7. Bigham M, Copes R. Thiomersal in vaccines: balancing the risk of adverse effects with the risk of vaccine-preventable disease. Drug Safety 2005;28:89–101.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  8. Chen RT, DeStefano F, Davis RL, Jackson LA, Thompson RS, Mullooly JP, Black SB, Shinefield HR. Vadheim CM, Ward JI, March SM. The Vaccine Safety Datalink: immunization research in health maintenance organizations in the USA. Bulletin of the World Health Organization 2000;78:186–194.[PubMed], [Web of Science ®], [Google Scholar]
  9. Chen RT, Glasser JW, Rhodes PH, Davis RL, Barlow WE, Thompson RS, Mullooly JP, Black SB, Shinefield HR, Vadheim CM, Marcy SM, Ward JI, Wise RP, Wassilak SG, Halder SC. Vaccine Safety Datalink project: a new tool for improving vaccine safety monitoring in the United States> The Vaccine Safety Datalink Team. Pediatrics 1997;99:765–773.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  10. Wassilak SG, Glasser JW, Chen RT, Hadler SC. Utility of large-linked databases in vaccine safety, particularly in distinguishing independent and synergistic effects. The Vaccine Safety Talink Investigators. Annals of the New York Academy of Sciences 1995;754:377–82.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  11. Young HA, Geier DA, Geier MR. Thimerosal exposure in infants and neurodevelopmental disorders: an assessment of computerized medical records in the Vaccine Safety Datalink. Journal of the Neurological Sciences 2008;271:110–118.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  12. Haut MW, Morrow LA, Pool D, Callahan TS, Haut JS, Franzen MD. Neurobehavioral effects of acute exposure to inorganic mercury vapor. Applied Neuropsychology 1999;6:193–200.[Taylor & Francis Online], [Google Scholar]
  13. Rossini SR, Reimao R, Lefevre Bh, Medrado-Faria MA. Chronic insomnia in workers poisoned by inorganic mercury: psychological and adaptive aspects. Arquivos de Neuro-Psiquiatria 2000;58:32–38.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  14. Powell TJ. Chronic neurobehavioural effects of mercury poisoning on a group of Zulu chemical workers. Brain Injury 2000;14:797–814.[Taylor & Francis Online], [Web of Science ®], [Google Scholar]
    Olczak M, Duszczyk M, Mierzejewski P, Meyza K, Majewska MD. Persistent behavioral impairments and alterations of brain dopamine system after early postnatal administration of Thimerosal in rats. Behavioral Brain Research 2011;223:107–118.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  15. Li X, Qu F, Xie W, Wang F, Liu H, Song S, Chen T, Zhang Y, Zhu S, Wang Y, Guo C, Tang TS. Transcriptomic analyses of neurotoxic effects in mouse brain after intermittent neonatal administration of Thimerosal. Toxicological Sciences 2014;139:482–465.[CrossRef], [Web of Science ®], [Google Scholar]
  16. Curtis JT, Hood AN, Chen Y, Cobb GP, Wallace DR. Chronic metals ingestion by prairie voles produces sex-specific deficits in social behavior: an animal model of autism. Behavioral Brain Research 2010;213:42–49.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  17. Verstraeten T, Davis RL, DeStefano F, Lieu TA Rhodes PH, Black SB, Shinefield H, Chen RT; Vaccine Safety Datalink Team. Safety of thimerosal-containing vaccines: a two-phased study of computerized health maintenance organization databases. Pediatrics 2003;112:1039–1048. [Google Scholar]
  18. Khan A, Sulkowski ZL, Chen T, Zavacki AM, Sajdel-Sulkowska EM. Sex-dependent changes in cerebellar thyroid hormone-dependent gene expression following perinatal exposure to thimerosal in rats. Journal of Physiology & Pharmacology 2012;63:277–283.[PubMed], [Web of Science ®], [Google Scholar]
  19. Sulkowski ZL, Chen T, Midha S, Zavacki AM, Sajdel-Sulkowska EM. Maternal thimerosal exposure results in aberrant cerebellar oxidative stress, thyroid hormone metabolism, and motor behavior in rat pups; sex- and strain dependent effects. Cerebellum 2012;11:575–586.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  20. Branch DR. Gender-selective toxicity of thimerosal. Experimental & Toxicology Pathology 2009;61:133–136.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  21. Geier DA, Kern JK, Hooker BS, King PG, Sykes LK, Geier MR. A longitudinal cohort study of the relationship between Thimerosal-containing hepatitis B vaccination and specific delays in development in the United States: assessment of attributable risk and lifetime care costs. Journal of Epidemiology & Global Health 2016;6:105–118.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  22. Thompson WW, Price C, Goodson B, Shay DK, Benson P, Hinrichsen VL, Lewis E, Eriksen E, Ray P, Marcy SM, Dunn J, Jackson LA, Lieu TA, Black S, Stewart G, Weintraub ES, Davis RL, DeStefano F; Vaccine Safety Datalink Team. Early thimerosal exposure and neuropsychological outcomes at 7 to 10 years. New England Journal of Medicine 2007;357:1281–1292. [Google Scholar]
  23. Barile JP, Kuperminc GP, Weintraub ES, Mink JW, Thompson WW. Thimerosal exposure in early life and neuropsychological outcomes 7-10 years later. Journal of Pediatric Psychology 2012;37:106–118.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  24. Geier DA, Hooker BS, Kern JK, King PG, Sykes LK, Geier MR. A two-phase cohort study of the relationship between Thimerosal-containing vaccine administration as a risk factor for an autism spectrum disorder diagnosis in the United States. Translational Neurodgeneration 2013;2:25.[CrossRef], [PubMed], [Google Scholar]
  25. Geier DA, Hooker BS, Kern JK, King PG, Sykes LK, Homme KG, Geier MR. A dose-response relationship between organic mercury exposure from Thimerosal-containing vaccines and neurodevelopmental disorders. International Journal of Environmental Research & Public Health 2014;11:9156–9170.[CrossRef], [PubMed], [Web of Science ®], [Google Scholar]
  26. Sukumaran L, McCarthy NL, Li R, Weintraub ES, Jacobsen SJ Hambidge SJ, Jackson LA, Naleway AL, Chan B, Tao B, Gee J. Demographic characteristics of members of the Vaccine Safety Datalink (VSD): a comparison with the United States population. Vaccine 2015;33:4446–4450. [Google Scholar]
  27. Centers for Disease Control and Prevention. Hepatitis B virus: a comprehensive strategy for eliminating transmission in the United States through universal childhood vaccination. Recommendations of the Immunization Practices Advisory Committee (ACIP). MMWR Recommendations & Reports 1991;40:1–25.
  28. Geier MR, Geier DA. The state of polio vaccination in the world: the case for continuing routine vaccination. Toxicology Mechanisms & Methods 2002;12:221–228. [Google Scholar]