Vaccination~ by Suzanne Humphries M.D.

Vaccination~ by Suzanne Humphries M.D.

Most of the medical profession claims the issues surrounding vaccination have been “settled long ago, and laid to rest.” After my experiences in the hospital system and thoroughly examining both sides of the vaccination debate, it is clear that that isn’t the case.

Appearing in Issue #42. Order A Copy Today

The history of vaccination is more complicated than most people understand. The anti-vaccine movement is hundreds of years old. It heated up in the 1800s, when parents in the U.K. became fed up with watching their healthy infants and children become ill or die shortly after getting smallpox vaccinations, or later get sick from smallpox anyway. Parents and doctors who refused smallpox vaccines risked losing their homes, furniture and livelihoods if judges ruled against them.

The smallpox vaccines were made from pus scraped off of diseased cows’ belly sores, contaminated with disease matter from a variety of animals (and in some cases, humans). The smallpox vaccine history is not what you think it is, if you think vaccines wiped out smallpox.

Doctors and those administering vaccines are supposed to obtain “informed consent” before vaccinating. Informed consent is not possible, because parents are not given all the information they require to understand the most important issues.

I do not consider it my place to tell anyone whether to vaccinate or not. It is my place to understand as much as I can about vaccines and give people a more complete understanding from which to make their choices. This has never been a priority to the public health services. In fact there is ample documentation that the priority was quite the opposite, and actually to quell “any possible doubts, whether well founded or not” regarding vaccines. That priority has placed many lives in jeopardy, as major problems with vaccination were and are overlooked by vaccine policy makers.

There are many problems with the science that underpins vaccine information. I’ve yet to meet a pediatrician who is informed enough to offer informed consent. Infant immunity has been misunderstood by immunologists, as the immunology literature admits to. Only recently have some important questions been answered about why infant immune systems don’t function like adult ones. There is good reason for the tolerance that an infant has, and the answer is not to interrupt the program with aluminum and vaccines to ramp it up. Doing so is now known to have long-term consequences.

There is a paucity of studies comparing nevervaccinated children with partially or fully vaccinated children. In terms of safety studies, a major issue is that most vaccine studies use another vaccine as the control placebo, or use the background substance of the vaccine. There is a recent study, published in 2012 by Benjamin J. Cowling in Clinical Infectious Diseases, where a true saline placebo was used. That study showed no difference in influenza viral infection between groups, but, astonishingly, it revealed a 5–6 times higher rate of non-influenza viral infections in the vaccinated. It is no small wonder more true placebos are not used in vaccine research.

In the 2012 article “Neonatal outcomes after influenza immunization during pregnancy: a randomized controlled trial,” published in the Canadian Medical Association Journal (CMAJ), we see a clear example of how false placebos are regularly used. Needless to say, giving untested vaccines which can be unknowingly contaminated, and with unproven effectiveness, is a “medical experiment,” and in my opinion, violates the core principles of the Nuremberg Code (informed and unambiguous consent). Most vaccines have never undergone carcinogenicity testing, for example, and likewise are rarely studied in pregnant women, which results in people taking vaccines, either by a proclaimed “emergency”; by a “public health” order from the WHO; by threat of imprisonment or loss of rights over one’s children; or by threat of being abandoned by the medical professionals providing care.

“Informed consent” is devoid of all meaning when people are tricked into taking vaccines by the use of misleading or frightening “information.”

Parents must learn the ways to take care of their children when they get the common childhood illnesses, whether they vaccinate or not, since vaccinated children can still get the diseases they were vaccinated against. In the case of unvaccinated children, who experience childhood maladies, effective home nursing most often allows children to recover naturally, and in most cases, the child will have long-term immunity.

Some vaccine policies have robbed teenagers and adults of the opportunity to get re-exposed and continue with natural immunity. For example, in mothers who were vaccinated against measles, placental transfer of antibodies is limited to a few months instead of more than a year in naturally immune mothers. Sometimes, mothers’ breast milk is devoid of the necessary antibodies they need to protect their newborns—especially if those mothers were vaccinated in childhood.

The above exemplifies but one of the many potential consequences we face as a result of vaccination for measles and other childhood illnesses, such as rubella.

Medical schools do not educate about the contents, dangers, effectiveness or necessity of vaccines. Most medical doctors are fearful of the natural childhood illnesses because they don’t have any idea how to safely assist patients through them. The limited mainstream treatment options I learned often caused the diseases to be worse than they had to be. Yet surprisingly, I discovered other methods which work extremely well, but were never presented as part of my medical education.

In a short article from Stanford Medicine, “Tapping the Immune System’s Secret,” the limitations of immunology are plainly spelled out. The public is repeatedly deceived in order to maintain participation in vaccination. All sorts of tactics are used. One of the most popular is to say that everyone should get vaccinated in order to protect the unvaccinated. This is commonly known as “herd immunity.” I have written an extensive article on herd immunity that can be accessed in the Pathways resource section.

Doctors repeat the advice, “We have to vaccinate them while they are young so the ‘take rate’ is high.” A case in point is an article for which I was interviewed in which one of Maine’s supposed top experts is giving misleading advice. In an article from Bangor Metro titled “A Shot to the Heart,” author Joy Hollowell also interviewed Dr. Jonathan Fanburg, president of the Maine Chapter of the American Academy of Pediatrics:

Concerns about how much a young child’s immune system can handle at one time have prompted some parents to stagger vaccinations. But Fanburg points out that there is no medical data to support the practice, adding that it’s actually more beneficial to vaccinate infants, rather than wait until they are older. “Children have a better ‘take’ of vaccines in their first two years of life,” he says. “There is a higher rate of immunogenicity, which is the child’s ability to produce antibodies to the vaccine antigen.”

Dr. Fanburg seems to lack understanding as to how an infant’s immune system develops and why. If he understood, he would pause for some time before making such a dogmatic statement.

A baby’s immune system produces only very small amounts of IL-1B and TNF-alpha. There was a time when experts thought that this was simply a defect in all newborn humans. In 2004, a study published by Lakshman Chelvarajan suggested that if vaccine manufacturers added various immune system kickers into vaccines, this would solve the problem and fix these perfectly normal children’s immune systems, which are so often described as being “defective” or “inadequate,” although they are completely age-appropriate, with characteristics shared by all land mammals.

Subunit vaccines like HepB, Strep Pneumo, Hib and Meningococcal have potent “adjuvants,” such as aluminum. Without them, the baby’s immune system sits there and does nothing. An adjuvant creates a red-alert situation, forcing the infant’s innate immune system to respond opposite to the way it should function in the first year of life. Pro-vaccine immunologists see nothing wrong with this.

By 2007, Chelvarajan was seeing things differently. In the last paragraph of a study published in the Journal of Leukocyte Biology, he wrote that whereas in the past, he had considered this a “defect,” he now considered it an important developmental program:

This anti-inflammatory phenotype may be beneficial to the neonate at a time when tissue growth and remodeling events are taking place at a rapid pace…thus the inability of the neonate to respond to infection with encapsulated bacteria may be the risk the organism takes for successful development.

In order to adjust to the world appropriately, an “anti-inflammatory phenotype” is critical to an infant. Breast milk acts as a stand-in innate immune system, which protects the baby from toxin-mediated and other diseases by supplying anti-inflammatory substances in the milk, along with other immune particles. These prevent bacteria and viruses from adhering, or kill them outright.

This protects the baby, acting as “in loco” defense while the infant immune system is being programmed to know self from non-self. This same pattern of development is seen in laboratories where they study non-human mammals, and is ubiquitous across mammals, showing that the anti-inflammatory phenotype is crucial to successful survival both short and long term.

A more recent article published in Nature by S. Elahi in 2013 shows that infant immune cells have full functional capacity, but are clamped down by design, while the infant immune system is learning to distinguish between “self,” healthy commensal microorganisms, and what should later be attacked by the activated and trained immune system.

During this period of “clamping,” which according to Dr. Elahi, is approximately two human years, the infant is well compensated by the mother’s human milk, which continues the educational process and kills unwanted organisms. What then, is the effect of vaccines, which interfere with the quiescent state of the infant immune system’s master plan, adding large amounts of aluminum?

With breast-milk support, an infant immune system develops appropriately and systematically— in its own due time, according to the genetic program placed in the baby at conception. What is that master plan? To enable the infant to safely transition into immunological independence with the minimum level of inflammation possible. Can that system be derailed? Yes it can. What can derail it? Anything which triggers an inflammatory response in the mother while she is pregnant, and in the baby by the use of a vaccination.

Ironically the medical research is very clear about one thing. It’s not the “infection,” per se, that causes problems. It’s the activation of the immune system. How do they know it’s not just the infection? Because stress, toxins and other non-infectious antigens can trigger the immune system cascade in very similar ways to infection.

If it is important for successful development of a baby to allow the risk of infection by not allowing two key parts of the primary infection defense to “fire,” what’s the other risk you might take, if you force an immune system to do something it’s not supposed to do? A vaccine, by definition, causes repeated, chronic inflammation at set time intervals. Vaccines are designed to create peripheral inflammation, and vaccine adjuvants and antigens can cause brain inflammation, and create allergies and autoimmunity—resulting in constant inflammation all around the body. For some children vaccines can also cause mitochondria to stop working properly.

You might now be thinking: If a baby’s default position is to not respond to toxin-mediated bacterial diseases, what chance does a baby have to survive in this world? If you would like to learn more about neonatal immunity, I invite you to read a three-part article accessible in the Pathways resource section, and take note of the medical articles referenced.

Pro-vaccine doctors sometimes cite “peer-reviewed literature” to supposedly prove their point, yet a closer look at their own literature often proves otherwise—as does a closer look at the sick population of vaccinated children they supposedly care for. Furthermore, a close look at medical textbooks through the decades reveals a very interesting trend. In the 1920s and ’30s, doctors were often quite relaxed over diseases which today are presented as more deadly than the plague. Many grandparents today are completely bemused at the way the medical profession describes infections which were, to most of them, straightforward holidays off school.

This is not stating that there were never serious consequences. There sometimes were. However, today, most parents erroneously believe that every child will die from diseases which most grandparents found were nuisance value only.

The medical system now considers measles more dangerous than the plague, and the most dangerous disease known to man. Yet there is no need to be afraid of measles, because well-nourished children who get adequate vitamin A have an unremarkable course to recovery. Boredom might be their biggest whine.

I have discovered that whooping cough isn’t something to be scared of either. In the days when my only tool was an antibiotic, whooping cough occasionally caused me considerable concern, but not today. I’ve watched many parents all over the world treat whooping cough simply by using high doses of vitamin C and occasionally homeopathy. They see rapid improvement and no serious complications. But you will not read about these cases in peer-reviewed literature and your doctor doesn’t know about them, because sick children—the ones they see and often create—are the only ones counted in the morbidity statistics. Healthy children who uneventfully recover are not seen by the medical system, and therefore are not counted.

The serious consequences from most childhood diseases come from just a few things: infant formula, cow’s milk, common medical drugs (especially antibiotics), malnutrition, vaccines and a lack of knowledge about simple methods of home nursing.

All of these barriers to recovery are completely avoidable in the United States and many other countries, and that is why we see so many healthy children who were never vaccinated, when we take the time to look.

In the accompanying chart, you can see how mortality for the common illnesses declined significantly long before the vaccines were created.

There a few common misconceptions about not vaccinating:

1. You are putting other people at risk by not vaccinating.

At risk for what? Chicken pox? Ask your grandmother if she knew anyone who died from measles. Different diseases have different degrees of severity in different age groups. The misconception that “if you don’t vaccinate, you place others at risk” is based on an assumption that vaccinated people do not get the disease they were vaccinated for. Did you know that a controlled study published in BMJ in 2006 showed that of all the whooping cough that was diagnosed, over 86 percent of the children were fully vaccinated and up-to-date for the whooping cough vaccine? There are similar studies showing that mumps and measles outbreaks often affect the vaccinated. People who are vaccinated can have their immune systems altered in a manner that leads to susceptibility to other infectious diseases, and can also leave them vulnerable to the disease they were vaccinated for, due to a phenomenon called “original antigenic sin.” Original antigenic sin is where an injected vaccine antigen programs the body to react in a manner that is incomplete, and different to the natural response to infection. When the vaccinated contact that disease again, they are unable to mount an effective response to the pathogen because vital first steps are missing. The whooping cough vaccine is an example of this.

A noteworthy study was published by Jason Warfel in 2013, looking at baboons, which are susceptible and manifest whooping cough like humans do. In the Warfel study, baboons who were either vaccinated or not vaccinated were later exposed to pertussis (whooping cough) bacteria, something that cannot be done experimentally in humans (due to ethical considerations), but which yields very important data. Expectedly, the baboons that had never been infected got the cough and remained colonized with bacteria for a maximum of 38 days. Baboons that were previously vaccinated and immune vaccine-style, became colonized upon later exposure for a longer time than the naïve baboons: 42 days. However, unvaccinated baboons that recovered naturally and were later exposed to the bacteria did not become colonized at all—zero days.

So, who is providing better herd immunity in the face of bacterial exposure? Vaccinated individuals who presume they are immune, yet remain asymptomatically colonized for 42 days, spreading bacteria? Unvaccinated kids who get infected and remain colonized for 38 days? Or the naturally convalesced who are not able to be colonized and therefore do not spread bacteria at all upon re-exposure? Better still: Natural convalescence makes for decades-longer, more solid immunity than vaccination.

Many vaccine enthusiasts like to invoke the term “herd immunity” to make the argument that the non-vaccinated pose a risk to the vaccinated. But the concept of herd immunity has no relevance to the vaccinated, as it was coined in reference to natural immunity in populations and what level the least epidemics occurred. There is no evidence whatsoever that having an 85 percent or 95 percent vaccination rate protects from outbreaks. This theory has been disproved time and again in highly vaccinated populations.

2. The non-vaccinated spread disease.

Actually it is the opposite. Live vaccines are known to spread to close contacts. One example published in 2011 in Science Direct addresses this, concluding that in a mumps outbreak in the Netherlands, “the risk of a close contact becoming infected by vaccinated patients was small, but present.”

We also know that in pertussis those who are vaccinated are more likely, due to original antigenic sin, to be carriers of the bacteria longer than the nonvaccinated, even when asymptomatic. In his article published in Clinical Infectious Disease in 2004, author James Cherry pointed out that adults, re-vaccinated against pertussis, don’t develop any antibacterial activity whatsoever. He went on to explain why: The current vaccines contain a few antigens, which create original antigenic sin, whereby the immune response to the vaccine is abnormal. That first-learned response then becomes the default position the immune system takes, on future booster shots. So in the case of the whooping cough vaccines, there are key protein virulence factors which have not been included in the vaccines, including ACT, TCF, TCT, BrkA and DNT.

Because the first three are not included, the default immune response does not prevent colonization. Furthermore, Cherry stated that the original antigenic sin results in the vaccinated being unable to clear the bacteria from their lungs. The non-vaccinated have immunity to all the front-line virulence factors, and very quickly clear the bacteria on re-exposure.

Mothers who have been vaccinated may develop surrogate markers which can be measured in a laboratory, but these do not guarantee efficient immune responses after exposure to the natural disease, because their first “learned response” was incorrect. Furthermore, they are still not sure what the surrogate marker actually is for pertussis.

There is similar information on measles, the other disease that has been portrayed by the media as a danger to the population due to non-vaccinated children. But this information is not accurate, nor is measles a dangerous disease in people who have sufficient vitamin A. Another author, B. Damien, pointed out in the September 1998 issue of the Journal of Medical Virology that the vaccinated are 5 to 8 times more susceptible to asymptomatic infection than the non-vaccinated. How then, are the non-vaccinated solely responsible for the recent outbreaks in measles?

Many vaccines are said to be “attenuated,” or modified-live, and supposedly do not infect, but over the decades we have seen how those attenuated viruses mutate once they are in a human and can spread more virulent disease than what is being vaccinated for. The oral polio vaccines in Nigeria today are a case in point. But this can happen with any attenuated viral vaccine.

The original Salk polio vaccines were supposed to be killed vaccines, and yet they infected thousands of people, killing and paralyzing more than 200 of them. This figure is thought to be a gross underestimate of the damage done.

It is not uncommon to see a child recently vaccinated for chicken pox develop shingles or chicken pox. I’ve also seen the shingles vaccine (which has 14 times the amount of virus as the chicken pox vaccine) provoke shingles in an elderly woman days after the vaccine was given. Strangely enough, it sent all of her doctors to start reading to see if shingles vaccines can cause shingles, because medical doctors know almost nothing about vaccines.

Here are things to consider when you hear of an outbreak of an infectious disease: How many of the affected were fully vaccinated, and how many people died or were put in the hospital? Were the cases verified with laboratory tests, or are the reports based on community doctor reports?

Another question to bear in mind is, Were the people hospitalized because the disease was really serious, or because the family didn’t know how to deal with it and responded to a medical profession hard-wired to believe everyone with that disease can die? In other words, was the admission to the hospital really necessary?

3. Deaths from these terrible diseases that once plagued humanity will return to pre-vaccine levels if we do not keep up the vaccines.

We can see from the graph on the opposite page that the mortality of these diseases was drastically declining prior to vaccination. In addition, you might want to know the more rational explanation for deadly disease decline in modern times. It’s not vaccination; it’s hygiene. In a 2002 article published in The Lancet, “What is the evidence for a causal link between hygiene and infections?” authors Allison E. Aiello and Elaine L. Larson offer the epidemiological evidence between hygiene practices and infections.

Here is something else you may not have been informed of by your healthcare professional: All the reduction, even for tuberculosis, was achieved before vaccines of any sort were offered in the U.S., and most of the reductions for all diseases were achieved before antibiotics became commercially available in about 1950 as well. So what did that? It wasn’t vaccines. Yet all the countries which used the BCG as front-line protection saw an identical decline to the one which we saw in the U.S. using no TB vaccine.

If you compare graphs for death declines in diphtheria and scarlet fever, they are almost identical. Yet there never was a widely used vaccine for scarlet fever. Scarlet fever—and its resulting complication, rheumatic fever—has clearly been shown in the medical literature to be nutritionally driven. This is why people who have had scarlet fever are primarily in war-torn, hungry and impoverished countries. In developed countries where rheumatic fever is an issue, it’s primarily seen among less-educated groups, whose nutritional understanding or access to good food is limited.

Yet undereducated people in stable social environments, without much money, who understand and follow effective nutritional pathways, will be on the scale of low susceptibility. It really is the nutrition and well-being that counts. It just so happens that low education, homelessness and poverty often coexist.

The reason rheumatic fever is a significant problem among poorer, less-educated, less-nourished groups is because poor nutrition is historically correlated with higher rates of rheumatic fever. All of us carry strep A regularly, but the well-fed amongst us don’t get scarlet fever, let alone its complication, rheumatic fever.

This point is documented enough to lay aside any concern over whether or not correlation implies causation.

Historically, in the case of infectious diseases, good nutrition has been and still is a major preventive factor. That has led to enormous declines of morbidity and mortality from most infectious diseases.

It’s not my place to tell anyone whether to vaccinate or not. But if people are going to choose wisely, they need to know the full ramifications of their options.


Vaccines: An Attorney’s Viewpoint

Vaccines: An Attorney’s Viewpoint

SOTN Editor’s Note:
The following exposé on vaccine safety and their inherent dangers is noteworthy because it is written by a Washington State attorney who really understands the profound legal ramifications. James Deal, J.D. wastes no time in completely deconstructing the many false assertions that are routinely presented by those government and corporate entities promoting  a super-vaccination agenda.

More importantly, Attorney Deal furnishes the American people with the substantive legal arguments which can serve as the basis for lawsuits against both the Pharmaceutical Industry and the U.S. Federal Government.  When considered in the aggregate, the implicit points of law delineated below constitute a legal foundation for a clear-cut criminal indictment.  Great harm is being inflicted on the children throughout the country by mandatory, state-sponsored vaccination programs.

No entity under the sun has the right or lawful authority to arrogate power unto itself to harm or injure, sicken or infect, paralyze or kill the people of this nation.  Not only is such conduct a serious breach of the social contract, it represents a profound violation of the public trust.  Vaccination programs therefore break the inviolable bond between the citizenry and the government.

You Cannot Generalize Pro or Con About All Vaccines

James Robert Deal J.D.

justice will prevail

The report below was recently sent to every representative and senator in the Washington legislature and to all the newspapers in Washington. Attorney James Deal believes that the personal or philosophical objection will be retained at the state level.

“They have all the money, but we have all the good ideas. If we persevere, we will succeed.”
~ James Robert Deal, J.D.


Anti-vaxxers oppose all vaccines. Pro-vaxxers favor all vaccines. No, it is not that simple. Pro-vaxxers admit that certain groups should not receive certain vaccines and that vaccine injury does happen, although it is “rare”.

Most so-called anti-vaxxers actually favor some vaccines but oppose others. Most oppose giving many vaccines all at one time. Most say they are only asking for safer vaccines.

Amid the name calling, there is a reasonable middle ground. Dr. Mark Geier, M.D., Ph.D., associated with Johns Hopkins and the National Institutes of Health, author of over a hundred peer reviewed journal articles, is a moderate we should pay attention to. (Go to YouTube and search for “Dr. Mark Geier Thimerosal”.)

Dr. Geier supports the measles-only vaccine, but he opposes the MMR, measles-mumps-rubella vaccine, because it has caused confirmed adverse reactions and death. Likewise, Dr. Gregory Poland, of the Mayo Clinic holds that the MMR is largely ineffective.

It is lazy language to say that vaccines are “safe and effective”, because that implies that all vaccines are safe and effective for all people. In fact, some vaccines have done great harm. If you doubt this, read the findings of the Vaccine Court, which has paid out around $3.0 billion to children for adverse reactions which admits were caused by vaccines. Go to and search for “measles-mumps-rubella” or “influenza”.  And read the package inserts that come with vaccine boxes. You may also read them online

In Europe only the polio vaccine is mandatory. Dr. Geier supports vaccination against polio. However, he is adamantly opposed to flu vaccines. The flu vaccine given almost universally uses Thimerosal as a preservative. Each dose of Thimerosal contains 25 micrograms of ethyl mercury. Multiplied by Avogadro’s Number, 25 mcg = 75 quadrillion atoms of mercury.

25 x 10-6 / 200 x 6.02 x 10-23

10-6 x 10-23 = 10-17

25 / 200 x 6.02 = .7525

.7525 x 10-17 = 7.5 x 10-16 = 75 x 10-15 =

75,000,000,000,000,000 = 75 quadrillion

The only safe amount of mercury is zero, and using mercury as a preservative is reckless, especially since it is given yearly, even to pregnant mothers, even though the package insert admits that the MMR has not been tested for fetal safety in pregnant women. Mercury passes through the placenta and into the fetus. There are flu vaccines which are mercury free.

The flu vaccine is big business, particularly the ones containing mercury. Some 300 million doses are sold, while only 20 million doses of all other vaccines are sold. In 1986 the National Vaccine Injury Compensation Program made vaccine manufacturers immune from most liability, and in 2011 the Supreme Court twisted the plain language of the Vaccine Act to make vaccine manufacturers, hospitals, and physicians completely immune from absolutely ALL liability, reasoning that vaccines in general – using the language of the Court – are “unavoidably unsafe”.

Dr. Geier points out that all flu vaccines are illegal. All vaccines must pass two double blind tests for safety and effectiveness. Because a new vaccine is developed each year in advance of the flu season, and because each vaccine assumes a prediction of which strains of flu will be present, there is no time to two double blind studies, which would take several years.

Our vaccines can contain aluminum, formaldehyde, MSG, antibiotics, and monkey kidney cells. The effort to develop safe and effective vaccines should continue, however, we must admit that we are still at a primitive stage in the development of vaccines, which is why mandating vaccination makes little sense.

The unvaccinated are blamed for spreading disease, however, every person injected with the MMR and other attenuated live virus vaccines develops a vaccine version of the disease, sheds viruses, and can infect others. It is not only the unvaccinated who are spreading measles, which is another reason why mandating vaccination makes little sense.

Measles is not a trifling malady, however, it is not Ebola. Measles cases and deaths from measles declined sharply before the measles vaccine was introduced in 1963. Relatively few die from measles.

Since 1986, Health & Human Services reports 669 deaths from the DTP, 84 deaths from flu vaccines, 80 deaths from the DTaP, 57 deaths from the MMR, 54 deaths from the Hepatitis B vaccine, and many more non-fatal adverse reactions. The science of vaccination is still in a primitive stage, and it is inappropriate for the state to force injection of a possibly harmful drug on behalf of mega-corporations which are completely immune from all liability for adverse reactions.

Further, one who is vaccinated sheds viruses, and so one can be infected not only by those who contract a wild case of measles but also by those recently vaccinated. Moreover, the MMR is not particularly effective “In an October 2011 outbreak in Canada, over 50% of the 98 individuals had received two doses of measles vaccine”.

The Los Angeles Times and the Everett Herald printed an article entitled “Vaccine ignorance proving deadly and contagious”. It was written not by physicians or scientists but by prominent members of the Council on Foreign Relations. It contains numerous inaccuracies – scientific, historical, and legal.

Thinking people support vaccines which are safe, effective, and necessary. Conversely, thinking people should oppose those vaccines which are not safe, not effective, or not necessary.

Law school taught me to break a question down into its component parts: Which vaccines are safe, effective, and necessary, and for whom? How deadly is the disease to be prevented? How likely are adverse reactions and how bad can they be? The CFR authors are uncritical cheer leaders for the $30 billion per year vaccine business, exhorting us to take all recommended vaccines unquestioningly and by the dozens and dozens.

The authors repeat slanders made against Dr. Andrew Wakefield, which were completely false. A recent NOVA special, “Vaccines – Calling the Shots”, repeats these now-disproven slanders, a case of lazy journalism. Recall that Wakefield wrote in the Lancet in 1998 that colitis and autism spectrum  disorders are linked to the combined measles, mumps and rubella (MMR) vaccine then in use.

Wakefield was denounced as a vaccine denier, although he supported and still supports the single dose measles vaccine, as well as other vaccines. He only opposed the MMR. Multiple vaccines given simultaneously can be more harmful than single vaccines. For questioning the safety of one vaccine, Wakefield was “lynched” by GlaxoSmithCline and the medical establishment. Wakefield’s results have been replicated in at least 28 studies done by scientists in other countries. Further, Wakefield has great insight in how to treat children who have had adverse vaccine reactions by treating the gastro-intestinal disease that accompanies adverse reactions.

Wakefield was expelled from the medical profession in Great Britain, however, John Walker-Smith, one of the co-authors of the offending 1998 study, challenged his expulsion and was recently reinstated, an indication that Wakefield could be reinstated if he applied. Wakefield works in Texas as a researcher and is suing Brian Deer, Fiona Godlee and the British Medical Journal for falsely accusing him of fraud.

The CFR authors also seem to be unaware that Wakefield was further vindicated recently when Dr. William Thompson of the CDC “came out”. Thompson was one of the authors of a CDC study which denied any causal link between vaccines and autism. Thompson admitted that in a 2004 article he and other authors had intentionally excluded already collected data, data which would have reversed their published conclusion that there is no vaccine-autism link. The mainstream media has glossed over the story of Wakefield’s vindication and Thomson’s confession.

A mother is not a vaccine denier if she questions the safety of a vaccine containing mercury, aluminum, MSG, antibiotics, eggs, or formaldehyde. Or Beta HCG hormone. Or the urabi virus . She is not a denier if her child is frail or has already had an adverse vaccine reaction and she chooses to opt her child out. She is not a denier if she questions giving children 49 injections of 14 vaccines by age six, including a vaccine at birth for hepatitis B, a disease usually infecting IV drug users. Nor is she a denier if she declines the CDC recommendation that she take the flu vaccine (containing mercury) when she is pregnant, even though the flu vaccine is not tested for safety for pregnant women and fetuses and the FDA advises it be used “only if clearly needed”.

Most are not harmed by vaccines, but some are. For proof read the decisions of the Vaccine Court, which has paid out some $3.0 billion and has acknowledged that specific vaccines have caused specific harms. See the disclosure inserts which comes in vaccine boxes. Ask your pharmacist for copies. Multi-dose flu vaccine contains a whopping 25 micrograms of mercury per dose, included as a preservative. That’s 74 quadrillion atoms of mercury. The single dose version contains under 1.0 micrograms, only 3 quadrillion atoms – still too much for me. The mercury in the flu vaccine passes through the placenta and is especially toxic to fetus and infant because their cells are dividing rapidly. Mercury affects cell division. The use of mercury as a preservative should be banned.

Some vaccines are ineffective. Discover Magazine reported that 73 percent of kids aged 7 to 10 who caught pertussis in 2012 in Washington had been fully vaccinated. The same is true for the measles vaccine. A child vaccinated with a live virus vaccine experiences a mild version of the infection and is thus contagious and infects others. Outbreaks of measles and pertussis probably come from the vaccinated, not from the unvaccinated. The artificial immunity conferred by vaccines wears off, and boosters are required, making vaccines a cash machine that generates $30 billion yearly.

A reasonable question to ask is this: If vaccines worked, those who favor indiscriminant vaccination should not object to those who choose not to be vaccinated.

The problem worsened in 1986. Before that date vaccine liability had always been decided according to state law regardless of which court the case was brought in. 1986 Congress federalized all vaccine liability claims. A law was passed requiring that all claims for vaccine harm go to a special “Vaccine Court”, where there was and is no jury and no pre-trial discovery. The statute of limitations is tricky and short, and the burden to prove a specific vaccination harmed a child is arbitrarily difficult. Vaccine makers are shielded against general liability and even for badly designing a vaccine. Claims are paid out of a fund built up with a tax on each vaccine dose sold. This has led vaccine makers to become reckless, to do insufficient testing of vaccines, and to industrialize the vaccine business.

Before 1986, vaccination had been a technology aimed at the most deadly and contagious diseases. Vaccines were to be put into use only after careful testing. Vaccines were and are needed when a potentially fatal disease progresses so fast the body cannot respond before death occurs. Because adverse reactions are inevitable, vaccines should not be used to prevent diseases which are rarely fatal. However, vaccine makers, newly exempt from all liability, turned necessary vaccination against the most deadly diseases into a mass-production money machine targeted against any and every conceivable disease.

Vaccine makers ship vaccines banned in the West to the Third World, such as the urabi strain MMR vaccine, the dangerous partially attenuated oral polio vaccine used in Pakistan, and a tetanus vaccine which causes miscarriages – none of which would inspire one to trust what vaccine makers say.

All drugs and all vaccines involve some risk which the CDC admits in its assurances that serious harm or death is rare. If the risk of taking the vaccine is greater than the risk of enduring the disease, one has the right to refuse to take the vaccine. Adults can refuse vaccination for themselves. They are the guardians of their children. They know their children’s frailties and previous bad experiences with vaccines. They have the right to opt their children out. If vaccinations work, there should be no objection if some choose not to be vaccinated.

Washington has recently made it more difficult for parents to decline vaccination for their children. Unvaccinated children can be sent home if there is an outbreak of a childhood disease in his or her school, which is odd since the CDC admits, in the case of pertussis, it is vaccinated children who are spreading the disease.

Despite all the evidence that some vaccines cause serious harm, many so-called experts exhort us that all vaccines are safe and effective, and most people stubbornly believe them. Why? Mark Twain explained it best “It’s much easier to fool someone than to convince them they have been fooled.

Examine the evidence for yourself and do your own thinking. Administration of vaccine in mass quantities should not be mandatory, and some vaccines should be banned outright.

The connection between the fluoride scam and the vaccine scam is that they are both run by mega corporations without ethical standards.

We should not be afraid to follow the science where ever it logically goes and be outspoken on other contaminations, such as Roundup, which I just learned is sprayed on non-GMO wheat as a dessicant, so most non-organic bread is loaded with Roundup.

SOTN: Alternative News & Commentary