VACCINES MUST BE SAFE BECAUSE THERE ARE VERY FEW IF ANY ADVERSE VACCINE REACTIONS EVER REPORTED, RIGHT?
If the FDA and CDC readily admit that only 1-10% of adverse drug reactions, including those for vaccines, are ever reported, yet over $3.5 billion has been paid out to date for vaccine injuries and vaccine fatalities, from a program that the vast majority of our doctors and citizenry is unaware of, and from a program in which less than 1/3 of vaccine injury and vaccine fatality cases is actually compensated, then how can it be said that vaccines are safe? In other words, with 90+ percent of vaccine-induced injuries and deaths going unreported, with most people completely unaware of being able to file a claim with the VICP, or finding out about the VICP after the brief 3-year statute of limitations for filing a claim has passed, and with the VICP being a government-run-and-rigged kangaroo court in which discovery is not allowed, the more than $3.5 billion in payouts is but the tip of the proverbial iceberg when it comes to what should have been paid out to date for vaccine-induced injuries and deaths!
How can vaccines be both safe, as touted by doctors, government regulators, and the media, andunavoidably unsafe, meaning inherently dangerous, as declared by the U.S. Supreme Court in 2011? Both statements cannot be true.
If vaccines are safe, why then do we have the1986 National Childhood Vaccine Injury Act, the Vaccine Adverse Events Reporting System, the Vaccine Injury Compensation Program, the Vaccine Injury Table, and lengthy sections on each and every vaccine package insert detailing adverse events, including death, that have resulted from those very vaccines? If vaccines are safe, then why do this Act of Congress, this reporting system, this compensation program, and these warning lists exist?
The hallmark of ethical medicine is that of prior, completely voluntary, and fully informed consent. The U.S. has agreed to uphold and abide by this standard of ethical medicine on numerous occasions, beginning in 1947 with the signing of The Nuremberg Code. This international code of ethics was the result of the world becoming aware of atrocious medical experiments performed on human beings during WWII without their consent, and often without their knowledge. To ensure that such crimes against humanity would never occur again, the Nuremberg Code was written and it states that “the voluntary consent of the human subject is absolutely essential.” Additional, similar codes of ethics have been signed since then by the U.S., most recently including The Declaration on Bioethics and Human Rights at the UNESCO Convention in 2005, which states in Article 6 under the section titled Consent:
Any preventive (which by definition includes vaccines), diagnostic, and therapeutic medical intervention is only to be carried out with the prior, free, and informed consent of the person concerned, based on adequate information. The consent should, where appropriate, be express and may be withdrawn by the person concerned at any time and for any reason without disadvantage or prejudice.
In Article 3 of this same Declaration it states: The interests and welfare of the individual should have priority over the sole interest of science or society.
Vaccines mandates, in and of themselves, with or without exemptions, are in complete violation of the Nuremberg Code and other international codes of ethics, as is any form of mandated medicine.
Part of that truth involves challenging the notion that it is desirable for humans to be infection-free. The immune system, like our muscles and our brains, needs to be challenged to become stronger and more efficient. However, the challenges must occur via natural means, not via artificial and damaging means. The current and unnatural goal of eliminating temporary, acute, immune-system-building infections has led to the development of permanent, chronic, immune-system-destroying diseases. So we must ask ourselves, do we want the former or the latter?
We must also ask ourselves, what benefits are we forever forfeiting when we interfere via vaccination in an attempt to try to avoid contracting infections naturally? To list but a few, one is forfeiting: permanent lifetime immunity; the future ability for females to pass on immunity to their baby both in the womb and via breastfeeding; contracting these illnesses during childhood, when they are mostly benign, and instead contracting them during adulthood, when they are far more serious; protection against and avoidance of many types of cancer, both during childhood and later on in adulthood; and, perhaps most importantly, the purity of one’s immune system, which can never be restored. Wow, that is quite a list of health benefits one forfeits when one chooses to vaccinate.
I also want to challenge the notion that vaccinations equal immunization. Not true at all, and that is why you will never hear me call vaccinations “immunizations”, because they are not. Vaccine “efficacy” is allowed to be determined by the presence of titers post-vaccination in small numbers of study subjects. Titers are concentrations of antibodies. However, the presence of elevated vaccine-induced titers does not mean a person is now immune from that which he was vaccinated against, it simply means his blood has been purposefully and artificially tainted by a vaccine. In reality, people with low to zero titers for a certain infection can remain uninfected when exposed to that illness, and conversely, people with extremely high titers for a certain infection can contract the illness when exposed. Therefore, the presence of vaccine-induced titers offers no proof of vaccine efficacy…yet, it continues to be used as proof of efficacy…and vaccine recipients continue to be duped…and poisoned.
Furthermore, to the best of my knowledge, there has been no research comparing vaccine-induced titers to titers acquired via natural means, such as through breastmilk and/or through exposure to natural infection. Such a comparison study is required before claims of any kind can be made about vaccine-induced titers.
YOU REALLY NEED TO BE A SCIENTIST OR MEDICAL DOCTOR TO QUESTION VACCINE SAFETY OR EFFICACY, DON’T YOU?
Today, I would like to begin by reassuring you that you do not need to be a PhD chemist or biologist, or a medical doctor, or some type of genius to understand that what is going on with vaccines is not scientific, is not proven, is not safe, is not working as claimed, is not ethical, and is not wise. All that is truly needed is a basic level of common sense, parental instincts that have not been demeaned, grossly manipulated, and obliterated by doctors and others, and the willingness and ears to hear the truth.
THE MEDIA DOES NOT SAY ANYTHING ABOUT VACCINE INJURIES OR DEATHS; SO HOW DO PEOPLE ACTUALLY KNOW ABOUT VACCINE ADVERSE REACTIONS?
If vaccines are safe, why are parents worldwide using every alternative media source possible to tell their tragic stories of what happened to their children, and/or themselves, post-vaccination? Mainstream media refuses to cover these extremely prevalent stories, but that has not stopped parents, and others, from getting the word out. The stories are endless, they are tragic, and they did not need to happen. My guess is that Del Bigtree will be sharing some stories from being on the road with the Vaxxed Team when he speaks this afternoon, and I will share my son’s story later in my presentation.
WHEN YOU OR YOUR FAMILY MEMBER GETS INJURED FROM A VACCINE, YOU CAN SUE AND COLLECT COMPENSATION AND DAMAGES FROM THE DRUG COMPANIES, RIGHT?
If vaccines are safe, why did the U.S. Congress remove liability from those who make and administer vaccines in 1986? For those who are not familiar with the 1986 NCVIA passed by Congress, it came about as a result of vaccine-making pharmaceutical companies being sued time and again for their dangerous and deadly vaccine products. Losing costly lawsuits for their vaccine products was not good for PR or for the bottom line. As a result, they and their well-paid lobbyists whined to and pleaded with Congress to shield them from liability for their vaccine products, claiming vaccines were needed to ensure public health. Unbelievably, at the very time when Congress should have ordered an immediate moratorium on all vaccines to get to the bottom of why so many children, and people of all ages, were being injured and killed by vaccines, they instead indemnified those who were making and administering the dangerous and deadly vaccines. Insane! Unethical! So very wrong! Not surprisingly, with no liability to worry about, leaving them with zero incentive and zero accountability to make safe vaccine products, vaccine makers began churning out new vaccines, and within just a few short years, our nation’s vaccine schedule for children nearly tripled! Tragically, my 3 children were born just after this tripling occurred, in 1992, 1994, and 1996.
Those who vaccinate should feel oh so protected, and if they don’t, then at some level, they knowthey have been duped into allowing faulty products to be injected into their children and/or themselves. Here’s another way to look at it: how is my taking a medicine going to make your medicine more effective? Answer: it isn’t.
If vaccines work, why in nearly every “outbreak” of pertussis, measles, and mumps in our country has the majority, if not a full 100%, of those infected been vaccinated? That should not be the case if vaccines work as claimed, and it makes null and void the theory of vaccine-induced herd immunity.
If vaccines are safe and effective, why do the vaccinated often contract the diseases for which they were vaccinated? One of my favorite examples of this is to read the list of adverse reactions on the flu vaccine package insert. Virtually ALL the symptoms of the flu are listed right there, in plain print, under adverse reactions!
Booster shots are proof of vaccine failure. They are proof that vaccines don’t provide lifetime, or even lengthy, immunity. They are proof that vaccines are not effective for all, if any, or for any known or proven amount of time. And once again, the ridiculous yet oft-touted claim of vaccine-induced herd immunity is blown to bits by the continual addition of and need for booster shots.
If vaccines work, why are 5 DTaP vaccines needed by age 5, with another TDaP at age 12, and additional TDaPs every 10 years? And why do those following that intense vaccination schedule still contract, harbor, and spread pertussis? That is proof that vaccines don’t work, and that the powers that be know it.
If vaccines are safe and effective, why do those who have received live-virus vaccines, such as the chicken pox, measles, mumps, rubella, shingles, nasal flu, rotavirus, yellow fever, and possibly other vaccines, shed and spread the diseases for which they were vaccinated to others, for up to 6 weeks, perhaps for much longer? And since viral shedding by vaccine recipients of live-virus vaccines is a known and documented fact, why then are recipients of live-virus vaccines not required to self-quarantine, at home, until blood, saliva, and urine tests conclusively confirm that they are no longer capable of shedding and spreading the diseases for which they were vaccinated?
ARE THOSE WHO HAVE RECEIVED THE DTAP AND TDAP VACCINES ABLE TO HARBOR PERTUSSIS IN THEIR THROATS AFTER ENCOUNTERING PERTUSSIS POST-VACCINATION?
Those who have received the DTaP and TDaP vaccines are able to harbor pertussis in their throats after encountering pertussis post-vaccination, enabling them to infect others while remaining asymptomatic, which is extremely dangerous as neither they nor those with whom they come in contact are aware that they are contagious. This fact blows the vaccine profiteers’ theory of “cocooning a newborn” right out of the water. In actuality, those vaccinated with pertussis-containing vaccines pose a real threat to infants, the immune-compromised, and the elderly. To make matters worse, those vaccinated with pertussis-containing vaccines are more susceptible to the rarer and more virulent strains of pertussis against which vaccines offer no protection…and those more virulent and dangerous strains are the very ones they might be spreading to unsuspecting others.
DO VACCINE MANUFACTURERS AND THE GOVERNMENT COMPARE THE HEALTH OF VACCINATED VS THE UNVACCINATED POPULATIONS?
And the real kicker, as I mentioned earlier, which bears repeating…there has never been a comparison study of the unvaccinated versus the vaccinated. That is because the vaccine profiteers know that the health, development, fertility, and longevity of the completely unvaccinated are far superior to that of the vaccinated. As a result of that knowledge, they have managed to keep that study from being done for more than seven decades. Without such a comparison study, absolutely no safety, efficacy, or necessity claims about vaccines can be made.
IF VACCINES ARE SUPPOSED TO BE MONITORED POST-LICENSURE AND POST-MARKETING, WHY ARE MULTIVALENT VACCINES ALLOWED?
A multivalent vaccine is a vaccine that contains more than 1 vaccine, up to 6, given via a single shot. And why is more than one vaccine, be it monovalent or multivalent, allowed to be given at a time? With such careless and reckless practices the norm, how can it ever be determined which vaccine might be problematic for a recipient if more than one is administered at once? Answer: It can’t be, and that is why it is allowed. Such practices are an excellent way to muddy the waters and keep inconvenient and horrendous truths that the vaccine profiteers don’t want you to know from being exposed. Additionally, the average parent’s warning bells sound more and more loudly with each subsequent painful jab to their precious child. Thus, the idea was hatched to cram as many vaccines into one syringe as possible to make the barbaric practice of vaccination less repugnant for the parent, and to make unpleasant and tragic results more difficult to pinpoint back to a particular vaccine.
If lots are separated, how can it be quickly determined when there is a problematic “hot lot” so that an immediate warning and recall can be issued? A “hot lot” refers to a lot that is causing more adverse events and deaths than usual. Answer: With lots separated, hot lots can’t be quickly identified and recalled, and that is done on purpose. In the late 1970s, vaccine maker Wyeth appears to have developed a plan to evade hot-lot accusations. Why? Because in 1979, 11 babies died within 8 days of a DPT shot. Nine of them had been vaccinated with the same lot of pertussis vaccine, Wyeth #64201. Five died within 24 hours, 4 from the same lot. The following is from a Wyeth Internal Correspondence dated 8-27-79: “After the reporting of SIDS cases in TN, we discussed the merits of limiting distribution of a large number of vials from a single lot to a single state, county, or city health department and obtained agreement from senior management staff to proceed with such a plan.” I have a friend and colleague who for years worked in the pharmacy at a hospital. She confirmed that the only drug that is shipped in separated lots is vaccines. That is unconscionable, not to mention highly dangerous.
IF VACCINES ARE SUPPOSED TO BE MONITORED POST-LICENSURE AND POST-MARKETING, WHY AREN’T THERE… POSTERS IN EVERY DOCTOR’S OFFICE, HOSPITAL, AND PHARMACY WITH INFORMATION ABOUT VAERS AND THE VICP?
Surely our government regulatory agencies, so concerned about our health, would want us to know how and where to alert them about problems with vaccines, right? Why does the majority of doctors not know about VAERS or the VICP? Why are they not required to report any and all adverse events, including death, after administering vaccinations? Why are they not required to inform parents and all vaccine recipients about VAERS and the VICP? Why are they loathe to properly inform about, recognize, acknowledge, admit, report, and treat vaccine-induced injuries and deaths? Why after someone is vaccine injured or vaccine killed is there absolutely no follow up from any government agency to determine what happened so that it can be prevented in the future? Answer: The complete and utter lack of monitoring vaccines post-licensure and post-marketing is purposeful. It is intentional. Our government regulatory agencies, in tight cahoots with pharmaceutical companies and their paid lobbyists, and with the willing compliance of doctors, nurses, pharmacists, and their associated trade industry groups, choose to turn a blind eye to vaccine-induced injuries and deaths. They choose to keep well-hidden the vaccine adverse events reporting system and the vaccine injury and death compensation program. These various entities, groups, and individuals are complicit in refusing to seek out, become informed about, acknowledge, admit, or allow anything that will undermine the public’s trust in vaccines and jeopardize the vaccine profits from which they all profit handsomely, to the tune of billions of dollars per year.
Not one vaccine has ever been tested according to the scientific gold standard, that of a double-blind, placebo-controlled study. Yes, you heard that correctly, not one.
The myriad combinations in which vaccines are administered have never been tested, either. For an infant at a “catch up” appointment, meaning they missed a “well-baby” appointment at which vaccines would have been administered, that can mean receiving up to 13 vaccines containing 13 different viral and bacterial infections, at once, injected via 8 separate needles. That is the equivalent of taking up to 13 medications at once whose interactions have never been studied.
To make matters even more serious, the number 13 does not include the many other ingredients that accompany and worsen the effects of being injected with 13 viral and bacterial infections, ingredients such as mercury, aluminum, formaldehyde, anti-freeze, phenol, MSG, polysorbate 80, Triton X-100 detergent, food proteins, animal viruses and retroviruses, fetal tissue from aborted human babies, and more.
The number 13 also does not include ingredients that are not required to be listed on the label, but which are permitted under the cover of “trade secrets”. Undisclosed ingredients being injected into our children? Unacceptable, unethical, and terribly dangerous. Ask yourself, would you want your baby contracting multiple illnesses, up to 13, at once? Would you want your baby contracting multiple illnesses at once while also being poisoned at the same time? If you are following the CDC’s recommended schedule, you are allowing that.
Many vaccines contain mercury in the form of thimerosal. Thimerosal was patented in 1928, and has been used ever since, despite it being tested on humans only once, in 1929…a test in which all 22 subjects died within 2 days of receiving the thimerosal. Mercury is a known toxin and neurotoxin, with no safe amount for a human. It can kill when applied externally. With vaccines, it is injected internally. Claims that mercury has been removed from vaccines given to children are false.
Many vaccines contain ingredients that have never been clinically approved by the FDA. Defying common sense and violating basic safety and ethics standards, the FDA approves vaccines that contain never-proven-safe and known-to-be-dangerous ingredients. For example, there are two forms of aluminum adjuvants used in vaccines, aluminum hydroxyphosphate salt and aluminum oxyhydroxide salt. Neither has been clinically approved by the FDA, both are known toxins and neurotoxins, yet both are in vaccines approved by the FDA. These are but two examples, there are more.
BUT ALUMINUM IN VACCINES IS CERTAINLY SAFE SINCE IT’S VIRTUALLY EVERYWHERE (COOKWARE, SKIN CARE) AND IS HARMLESS, RIGHT?
Aluminum, used in the majority of today’s vaccines, is an undisputed toxin and neurotoxin. Its toxicity has been known for some 90 years. The two aluminum adjuvants mentioned above are used in vaccines for the express purpose of inducing toxicity. Permitting the use of aluminum in vaccines is akin to permitting lead paint in government approved toys and teething rings. Aluminum, like mercury, is also a known teratogen, an agent or factor that causes malformation of an embryo. Permitting its use in vaccines for pregnant women is akin to permitting that which causes spontaneous abortion and/or deformity of the fetus…thalidomide comes to mind. Yesterday, Dr. Stephanie Seneff discussed the possible role of TDaP and DTP vaccines, both of which contain aluminum, and both of which were recently recommended to be given to pregnant women in Brazil, as possible causes for the rise in cases of microcephaly there. Microcephaly is abnormal smallness of the head, a congenital condition, associated with incomplete brain development.
DOSEN’T THE DRUG INDUSTRY’S SAFETY TRIALS WITH PLACEBOS RULE OUT THE TOXICITY OF ALUMINUM IN VACCINES?
Aluminum adjuvants (not clinically approved and used to induce toxicity), monovalent and/or multivalent vaccines (improperly approved and containing unapproved ingredients, including those used to induce toxicity, and containing ingredients known to be toxic and neurotoxic), or a combination thereof are used as the controls in vaccine safety trials. A control is supposed to be a placebo, an inert substance which doesn’t cause harm or therapeutic effect. Neither an aluminum adjuvant nor a vaccine, nor a combination thereof, qualifies as a placebo, therefore, no valid safety claims can be made for any vaccine.
Vaccine making pharmaceutical companies are permitted by the FDA to do their own safety testing, with no oversight and no verification from a financially independent entity. As mentioned in the point above, they do not use placebos for controls. Nevertheless, when they say that the trial vaccine proved to be no more dangerous or deadly than the aluminum adjuvant, or other vaccine, or combination thereof, against which it was tested, they declare it safe. Is that how you want medical procedures for your children being declared safe? The FDA and CDC accept this current method of testing. They also accept that vaccines are not tested for carcinogenicity, mutagenicity, or impairment of fertility.
Of course not, you know that would cause brain damage, not to mention other problems. However, millions of mothers across America are allowing doctors to inject mercury and aluminum into their children, both of which are severely neurotoxic (mercury many more times so than lead…and yes, mercury is still in vaccines given to infants and children, in addition to those given to pregnant women). To make matters worse, mercury and aluminum are synergistically neurotoxic, meaning that when they are given together, as is often done during vaccination, their individual toxicity is made far worse by the presence of the other, many times worse. Interestingly, we are seeing record numbers of children in our country with brain damage, which manifests as: speech and language disorders, including complete lack of speech; attention, learning, and behavior disorders; social skills deficits; seizure disorders; OCD; extreme anxiety disorders; sensory processing disorders; tics; and of course, Autism. Coincidence?
Of course not, you know that cancer is often akin to a death sentence, if not the first go-round, then the times that often follow. However, millions of mothers across America are allowing doctors to inject formaldehyde, phenol, and MSG into their children, all of which are known carcinogens. To boot, recent tests have revealed the presence of glyphosate, one of the active and toxic ingredients in Round Up and other herbicides, in a number of vaccines, including very high levels of glyphosate in the MMR vaccine. Glyphosate is a highly-suspected carcinogen, shown to cause massive tumors in rats fed food laced with it. It is synergistically toxic when paired with aluminum, an ingredient found in the majority of today’s vaccines. It’s no wonder pharmaceutical companies don’t test to see whether or not their vaccine products cause cancer, they already know the answer. Instead, they simply write “not tested for carcinogenicity” on their package inserts, and our unethical government regulators let them get away with that. Interestingly, we are seeing record numbers of children in our country with leukemia, lymphoma, and other cancers. Coincidence?
WOULD YOU ALLOW SOMETHING THAT COULD CAUSE LIFE-THREATENING AUTO-IMMUNE DISEASES, SOMETHING LIKE ALUMINUM, TO BE INJECTED INTO YOUR CHILD?
Of course not. You know that auto-immune diseases are progressive and lead to premature death. However, millions of mothers across America are allowing doctors to inject not only aluminum, but also mercury, polysorbate 80, retroviruses from pigs, mice, monkeys, and other animals, DNA fragments from other humans, specifically from aborted fetuses, and from various animals, and laboratory-created live and killed viruses and retroviruses from both humans and animals, all of which are known to cause auto-immune diseases. Interestingly, we are seeing record numbers of children in our country with Type 1 diabetes, asthma, Crohn’s disease, juvenile rheumatoid arthritis, demyelination, ulcerative colitis, and many more auto-immune diseases. Coincidence?
WOULD YOU ALLOW SOMETHING THAT COULD CAUSE LIFE-ALTERING AND LIFE-THREATENING ASTHMA AND ALLERGIES TO BE INJECTED INTO YOUR CHILD?
Of course not. You know that both asthma and allergies severely restrict a child’s life in many ways and that both can result in death. However, millions of mothers across America are allowing doctors to inject food proteins (which the blood is incapable of breaking down into amino acids, resulting in inflammation), antibiotics such as neomycin, polymyxin B, gentamicin, and streptomycin, and toxic chemicals at the same time as adjuvants (e.g. aluminum), which are designed to artificially overstimulate the immune system, resulting in the chronic and sometimes fatal conditions of asthma and allergies. Additionally, new studies regarding what is called “molecular mimicry” continue to emerge, demonstrating that when protein fragments in vaccine antigens match protein fragments of proteins in the body, it sets the stage for allergies and other autoimmune problems. Interestingly, we are seeing record numbers of children in our country with asthma, life-threatening peanut allergies, numerous types of food allergies and food intolerances, and numerous types of environmental allergies. Coincidence?
WOULD YOU ALLOW SOMETHING THAT COULD CAUSE INFERTILITY, SUCH AS NONSTICK CHEMICALS AND SOLVENTS, TO BE INJECTED INTO YOUR CHILD?
Of course not. You know that you would never want to destroy your child’s future reproductive capabilities. However, millions of mothers across America are allowing doctors to inject their children with polysorbate 80, known to adversely affect fertility. And who knows what propylene glycol (antifreeze), Triton X100 (detergent), aluminum, mercury, foreign DNA fragments, and the myriad other vaccine ingredients do to one’s future reproductive ability, especially when injected in conjunction with polysorbate 80. We know that the HPV vaccine has caused Primary Ovarian Failure (which is premature menopause) and amenorrhea (the prolonged cessation of a female’s menstrual cycle) in girls and young women, rendering them infertile, and possibly sterile for life.
We know that tetanus vaccines given to girls and women in Kenya were laced with Human Chorionic Gonadotropin (HCG), rendering them sterile. How? Administering HCG via vaccination stimulates the production of antibodies to HCG, and these antibodies then cause the woman’s body to reject embryos, effectively sterilizing her. Such an HCG-laced tetanus vaccine is in actuality a contraception vaccine. Do you think any of these Kenyan women was told that prior to vaccination? To add to the evilness and deception, the Kenyan women were given a 5-dose tetanus program spread over a number of years, versus the 2-3 dose norm.
Clearly, those vaccines were being used for induced sterility and birth control without the girls’ and women’s knowledge or consent. Does any parent or vaccine recipient really know what is in the vaccines being injected into their child or themselves? It’s no wonder pharmaceutical companies don’t test to see whether or not their vaccine products cause infertility, they already know the answer. Instead, they simply write “not tested for impairment of fertility” on their package inserts, and our unethical government regulators let them get away with that. Interestingly, we are seeing record numbers of couples struggling with infertility issues. Coincidence?
WOULD YOU ALLOW SOMETHING THAT COULD KILL YOUR BABY TO BE INJECTED INTO YOUR OTHERWISE HEALTHY CHILD?
Of course not! Mothers would lay down their lives for their children; they don’t purposefully put them in harm’s way. However, millions of mothers across America are allowing doctors to inject their children with more and more vaccines, not knowing that each and every one carries the risk of death, even more so when combined, as they most often are. Interestingly, we are seeing record numbers of babies who are dying before their 1st birthday in the U.S., including many of “SIDS” and “SDS” (the labels that unethical doctors and unethical medical examiners use for vaccine-induced deaths instead of calling them what they are…i.e. vaccine-induced deaths). Coincidence?
The hepatitis B vaccine is recommended to be given to all newborns in the U.S. within hours of being born. It is only advised against for premature babies weighing less than 4.4 lbs. Hepatitis B is a disease that is contracted sexually and via the sharing of needles by drug users. If a mother has hepatitis B, she can pass it on to her baby. Despite the fact that the vast majority of newborns in the U.S. is at zero risk for contracting hepatitis B, the vaccine is recommended and/or mandated for all. Right there, you know something very wrong is transpiring…and that something is others’ wealth being prioritized over your baby’s health.
When you look at the pre-licensure trials for this vaccine for infants and children, you will notice that there were no controls, only vaccinated subjects. A mere 147 subjects were studied, which included only healthy infants and children, from infants up to age 10. I have to wonder how many of those were of an age group that couldn’t talk and were unable to describe their symptoms? The insert does not say. You will notice that in this study subjects were followed for a mere 5 days post-vaccination. Does that sound like a reasonable, safe, or sufficient amount of time to you? Such a severely-limited timeframe doesn’t even correspond with the Vaccine Injury Table used by the VICP, in which it is acknowledged that many vaccine injuries, including death, may take up to a week, a month, and up to 6 months post-vaccination to manifest. And of course some vaccine injuries, such as what doctors choose to call “Autism” versus the catastrophic vaccine injury that it is, may take even longer to fully manifest and be diagnosed. Thus, the 5-day time period used to monitor and assess study subjects is in no way sufficient or ethical…and it shouldn’t be allowed by government regulators.
Here are symptoms reported during the clinical trial, i.e. within the first 5 days post-vaccination: irritability, fever, diarrhea, fatigue/weakness, diminished appetite, and rhinitis (irritation and swelling of the mucous membrane of the nose). Would you wish even one of those on a newborn?
Perhaps much more importantly, however, are the adverse reactions that have been reported post-marketing, meaning after the vaccine was licensed and in use. I will be redefining some of the medical terms in layperson’s terms so you will have a better understanding of the horrors being reported after being vaccinated with Merck’s hepatitis B vaccine.
Immune System Disorders: hypersensitivity reactions including anaphylactic/anaphylactoid reactions (severe, potentially life-threatening, allergic reactions that can occur within seconds or minutes of exposure to something you’re allergic to), bronchospasm (spasm of bronchial smooth muscle producing narrowing of the bronchi, causing difficulty in breathing which can be mild to severe), and urticaria (a rash of round, red welts on the skin that itch intensely, sometimes with dangerous swelling, caused by an allergic reaction) within first few hours after vaccination; an apparent hypersensitivity syndrome (serum-like-sickness) of delayed onset, days to weeks after vaccination, including arthralgia/arthritis (joint pain/joint inflammation), fever, and dermatologic reactions such as urticaria, erythema multiforme (a type of hypersensitivity skin condition), ecchymoses (a discoloration of the skin caused by bleeding underneath), and erythema nodosum (skin inflammation in the fatty layer of skin which results in reddish, painful, tender lumps); autoimmune diseases including systemic lupus (a chronic inflammatory disease that occurs when your body’s immune system attacks your own tissues and organs; inflammation caused by lupus can affect many different body systems, including your joints, skin, kidneys, blood cells, brain, heart, and lungs), erythema (redness of the skin or mucous membranes caused by dilation and congestion of the capillaries), lupus-like syndrome, vasculitis (inflammation of blood vessels), and polyarteritis nodosa (a serious blood vessel disease in which the small and medium-sized arteries become swollen and damaged).
Gastrointestinal Disorders: Elevation of liver enzymes (indicating damage to the cells of or inflammation in your liver); constipation (which can result in inability to clear toxins and pain).
Nervous System Disorders: Guillain Barre syndrome (a condition in which the immune system attacks the nerves, considered a medical emergency, and can result in paralysis); multiple sclerosis (a demyelinating disease; it is an unpredictable, often disabling disease of the central nervous system that disrupts the flow of information within the brain, and between the brain and body); exacerbation of MS; myelitis including transverse myelitis (inflammation of the spinal cord which can result in permanent paralysis); seizure; febrile seizure; peripheral neuropathy (damage to the peripheral nerves which causes weakness, numbness, and pain in hands and feet) including Bell’s Palsy (damage to the facial nerve that causes one side of the face to droop); radiculopathy (a condition due to a compressed nerve in the spine that can cause pain, numbness, tingling, or weakness along the course of the nerve); herpes zoster (shingles); migraine, muscle weakness; hypesthesia (a diminished capacity for physical sensation, especially the skin); encephalitis (brain inflammation).
Skin and Subcutaneous Disorders: Stevens-Johnson syndrome (a life-threatening skin condition); alopecia (hair loss); petechiae (red and purple spots caused by bleeding into the skin); eczema (itchy, red, and dry skin caused by inflammation).
By the way, the two worst things for a developing infant are toxicity and inflammation, both of which vaccines are expert at causing.
Musculoskeletal and Connective Tissue Disorders: arthritis; pain in extremity.
Blood and Lymphatic System Disorders: increased erythrocyte sedimentation rate (results from inflammation in the body); thrombocytopenia (a deficiency of platelets in the blood, causing bleeding into the tissues, bruising, and slow blood clotting after injury).
Psychiatric Disorders: Irritability, agitation, somnolence (extreme sleepiness).
Eye and Ear Disorders: Optic neuritis (inflammation of the optic nerve); tinnitus (ringing or buzzing in the ears, often with hearing loss); conjunctivitis (inflammation or infection of the outer membrane of the eyeball and the inner eyelid, also known as pink eye); visual disturbances; uveitis (inflammation of middle layer of the eye).
Cardiac Disorders: Syncope (fainting); tachycardia (abnormal rapid heart rate unrelated to level of activity).
What is missing from this list is the Death category. How many of the aforementioned vaccine-induced injuries resulted in death? Not surprisingly, that category is noticeably and wrongfully absent.
AREN’T MEDICAL PRACTITIONERS REQUIRED TO TELL YOU ABOUT THESE SIDE EFFECTS AND GIVE YOU A CHOICE TO NOT ALLOW THIS VACCINE?
For any of you here today who allowed this vaccine for your child, were you told about all of these potential side effects your child might experience, and possibly have to live with for the rest of their life? Were you told that there was no control group used when studying its effects in those aged 0 up to 10 years? Were you told that only 147 subjects in this age group were studied during clinical trials? Were you told the post-vaccination surveillance time period was only 5 days? Were you even told how your child could contract hepatitis B, and the extreme unlikelihood that that would happen during their infancy, toddlerhood, and childhood? If not, was your doctor practicing ethical medicine? Should he be liability-free when administering this vaccine to his patients? If he weren’t liability-free, would he be administering it?
I am going to close by telling you the story of our middle child, Ryan, now 22 years old. Ryan was born a healthy baby with an Apgar score of 9. I had a natural childbirth with him, receiving no medications during labor or delivery. Immediately after birth, he was given a vitamin K shot, which might have contained aluminum. I do not know if the particular brand he received contained aluminum, as some do, because I was not told, and I did not know to ask…or to refuse the procedure…for which there was no evidence he needed. He was also given antibiotic eye drops, which I have since come to find out used to be given only to babies whose mothers had gonorrhea.
When he was 2 months old, I dutifully took him in for his 2-month “well baby” appointment. Looking back, with hindsight being 20/20, he would never be well again after that first of many vaccine poisonings. Up until that 2-month appointment, Ryan was a typical and normally-developing baby. He nursed well, slept often, and cried when hungry, tired, upon awakening, or needing to be changed. After that appointment, at which he received the whole cell DPT vaccine, the oral polio vaccine, and the Hib vaccine, together containing a total of 50 mcg of mercury, Ryan stopped crying…and I mean completely…
At 4 months old, Ryan received the DPT, oral polio, and Hib vaccines, again, which meant another 50 mcg of mercury. After this appointment, looking back at video footage, he was getting harder, instead of easier, to engage. Ryan was still not crying to get his needs met at this time, and would lie silently in his crib when put down, even if not tired, and when awake after a nap, until someone came to get him. He was an exceedingly quiet baby. And I just thought, oh, he’s so good!
At 6 months old, Ryan received the DPT and Hib vaccines, another 50 mcg of mercury. After this appointment, 2 very strange things began to happen. Ryan’s breath began to smell odd, a chemical smell of sorts…alcohol? Ammonia…which I now know was indicative of a serious yeast overgrowth problem in his gut. He also began to laugh hysterically in the middle of the night in his crib for no apparent reason…
At 12 months old, Ryan received a TB test and another hepatitis B vaccine, adding another 12.5 mcg of mercury to his load. After this appointment, Ryan stopped responding to his name, and his eye contact began to disappear. He began to stop looking up when his dad came home from work, and instead preferred to watch Wee Sing videos, mesmerized by them…as he still is today at age 22…
At 15 months old, Ryan received his first MMR vaccine and another Hib vaccine, adding another 25 mcg of mercury to his small body, along with 3 live viruses that would later be discovered to wreak immense havoc in the young children receiving them in unison. After this appointment, Ryan’s babbling, which wasn’t that frequent to begin with, began to disappear, and he was losing the ability to imitate sounds we’d make for him to repeat. It was around this time that Ryan began to open and close doors, drawers, and cabinets repetitively, and play with the same hammer and ball toy over and over again. He also began spinning in circles at times, unresponsive to his name, and to requests to stop, or to come here…obliviously spinning in his own little world…
At 18 months old, Ryan received another DPT, another oral polio, and another Hep B vaccine, for a total of 37.5 more mcg of mercury, and for a grand total of 237.5 mcg of mercury in an 18-month timeframe for a tiny baby. This round of vaccines nearly killed him…
I called the doctor that same day, very worried about my baby. I did not get past the receptionist. She told me that his reaction was perfectly normal, and not to worry. I called every business day for 10 consecutive days, and never got past the receptionist. On the 10th day, the receptionist literally yelled at me and said, “Mrs. Hayes, please stop calling this office. Anything that happens in the first 2 weeks after a vaccination is considered a normal vaccine reaction. Do not call this office again until day 15!”…
After this set of vaccinations at 18 months, Ryan’s vocalizations became near nil, with his only remaining verbal imitation being “ba ba ba”, and only after numerous requests to imitate us. His obsession with videos increased, and he learned how to hit the eject button endlessly, putting the same video in and out until stopped. His visual and depth perceptions were not normal. He would often watch his videos from an upside down or bent sideways position…
At 24 months of age, Ryan received the new Varivax vaccine, for chicken pox. This was despite the fact that he was taking the antibiotic Septra at the time for an ear infection, and his records show that he was prescribed another round of Septra shortly thereafter, for either the same, or yet another, ear infection. Vaccines are not to be given when a child is sick, yet Ryan’s doctor gave him a live-virus vaccine! The package insert for Varivax clearly states under “Contraindications” for vaccination “any febrile illness or active infection”. I still was not connecting the dots between Ryan’s vaccines and his subsequent regression and development of odd behaviors after every set of vaccines…
At 6’4” tall and 180 lbs., Ryan is a boy in a man’s body, with a functioning level of a 4 or 5 year old. He is fully dependent on others and must be supervised and cared for around the clock, without pause. He did not complete high school or go to college. He does not have a driver’s license, and never will. He is not capable of living independently, or earning a living, or even holding down a menial, part-time job. He will not get married or have children. As a matter of fact, he will never even go out on a first date. He was robbed of ever living a typical and independent life because he was poisoned and disabled by vaccines beginning in 1994 and continuing through 1996.
WHAT OBLIGATION DO WE ALL HAVE TO TELL OTHERS ABOUT THE UNNECESSARY RISKS OF VACCINES AND THEIR HARM TO OUR NATIONAL HEALTH?
Please join me in spreading the truth about the dangers, inefficacies, and lack of need for vaccines, and the truth about the vast corruption and deception that underlie vaccines from manufacture to mandate, and beyond. Please join me in working to not only ban vaccine mandates, but to ban vaccines themselves, as they never should have come to market. Please join me in working to repeal the 1986 NCVIA, which wrongfully removed liability from its rightful owners, and please join me to overturn the 1905 Jacobson vs. MA decision, which is often cited as justification for vaccine mandates, even though the 1947 Nuremberg Code should have made that decision null and void, forever. Your voice and your activism matter. Together, we must reach the tipping point to end this vaccine madness in order to protect the health of our children, people of all ages, and the future of our country. Laura Hayes