The Dangerous Reasons You Should Never Give Your Baby Tylenol After Vaccines

By the time babies reach twelve months of age, they will have received about two dozen doses of vaccines, if their parents follow the schedule recommended by the American Academy of Pediatrics (AAP) and the Centers for Disease Control and Prevention (CDC). Many parents trust the recommendations of their health care providers, who assure moms and dads vaccines are “safe.” These same doctors and nurses also recommend Tylenol for babies after their shots. [1]

However, countries whose infants receive the highest numbers of vaccine doses during infancy also have the highest rates of infant mortality.

Many health care providers encourage concerned parents to give their baby Tylenol to relieve pain, fever, and crying after vaccination. In just a moment, you will know why this common recommendation can be very dangerous.

Babies’ Amazing Survival Abilities

Babies are born with amazing abilities and protective mechanisms to help them survive and grow during the months after they are born. Many child development experts refer to this important time of mental growth as “the fourth trimester.” On a basic level, newborn humans are born with the rooting and sucking reflexes, instinctive survival mechanisms to help them eat. They have the parachute reflex to help them survive a fall. [2]

Babies are born already recognizing and preferring their mother’s voice. In fact, within 24 hours after birth, the sound of their mother’s voice activates the part of baby’s brain responsible for learning language. The lists of the fascinating abilities of babies are endless. [3, 4]

However, despite their amazing capacity to survive and thrive, babies bodies’ are not designed to handle the onslaught of injected chemicals contained in dozens of vaccine vials. policy. The CDC’s one-size-fits-all vaccination schedule does not consider babies’ genetics, unique biology, birth weight, family medical history, or other special concerns. It also fails to recognize the amazing antibodies breastfed babies receive in their mothers’ milk.

One Vital Protection for Babies

Human babies are born “prematurely,” in a sense, before their brains are done developing. At the time of birth, our babies’ brains are only 30 percent of the size of the mature, adult human brain. Babies may be born “helpless” in order for their heads to fit through the narrow birth canal. During their first year of life, babies’ brains almost double in size. [5]

The human brain contains a protective gatekeeper known as the blood brain barrier. Essentially, this security system lets important substances into the brain and prevents damaging substances from reaching brain tissue. Researchers do not conclusively agree whether or not the protective blood brain barrier is fully developed at birth. [6]

For the past hundred years, pediatricians and neurologists have believed that the blood brain barrier is not fully developed when babies are born. They have described it as “leaky” and “immature.” If this theory holds true, babies lack protection from an onslaught of vaccine ingredients, beginning just moments or hours after birth when they receive their first vaccination.

Evidence from 2010 suggests that the infant blood brain barrier may be more mature than pediatricians and neurologists had believed for the past hundred years.  Even if this is true, can it handle the onslaught of up to 27 vaccine doses during the first year of life outside the womb? [7, 8]

The Blood Brain Barrier Faces Dangerous Vaccine Ingredients

Vaccines contain chemicals that are not beneficial for children of any age, especially for infants. You can read a list of vaccine ingredients here, as published by the CDC.

The list includes substances such as human DNA; squalene, a known cancer-causing adjuvant; thimerosal, a form of mercury known to cause neurological damage; aluminum; chick embryo cells; formaldehyde; and cell cultures from human embryos and guinea pigs.

Vaccines also contain excitotoxins, including monosodium glutamate (MSG), substances which can overstimulate and damage or even destroy brain cells, which would likely be even more dangerous to a still-developing brain.

All of these substance may cross the infant’s blood brain barrier. Sadly, babies’ blood brain barriers may be even more challenged when their parents give them popular pain relievers, such as acetaminophen, commonly known as Tylenol®.

The Risks of Mixing Tylenol with Vaccines

The CDC recently advised parents that giving children Tylenol pain relief after vaccination may make the vaccines less effective. The pain reliever’s ability to prevent fevers causes suppression of the immune system, which also renders the vaccines less effective. [9]

A 2011 report from the US Food and Drug Administration (FDA) warned parents and health care providers that overdoses of liquid acetaminophen in babies of children caused liver failure and death. [10]

Disturbingly, a recent research study demonstrated that increased use of acetaminophen during a child’s first year of life has been linked to higher rates of asthma. In addition, despite the unclear and complex causes of autism, the use of acetaminophen during infancy has also demonstrated a possible link to higher rates of autism. [11, 12]

The causes for these links are still unknown, but scientists have proposed that the use of acetaminophen may cause “alterations in glutathione levels.” Other leading theories include that the use of this popular pain reliever also causes “effects on serotonin, suppression of COX2, and specific effects of acetaminophen breakdown products.”

In simple terms, glutathione is a molecule made of three amino acids, the building blocks of life. Our bodies produce this vital substance naturally. It helps us stay healthy and prevent disease, aiding our bodies to fight cancer, heart disease, dementia, and chronic disease. As a supplement, it has been used to treat autism, Alzheimer’s disease, and cancer. [13]

When babies are vaccinated, many vaccine ingredients may cross the blood brain barrier. When parents give their babies pain relief in combination with a vaccine, glutathione levels may be lowered or depleted, preventing this important “security guard” from removing vaccine toxins from the brain and other parts of the body.

In addition, parents may be unable to recognize adverse reactions to vaccines because acetaminophen conceals crying, fevers, and other symptoms.


The widely accepted use of acetaminophen pain relievers, such as Tylenol, has been shown in scientific studies to deplete levels of our bodies’ master antioxidant, glutathione. Parents should question the popular notion that dozens of vaccine doses in infancy are safe, and they should certainly research the damaging effects acetaminophen can have on the developing brain.



Photo Credit

About the author

Missy Fluegge

Missy Fluegge is the mom of three children who have taught her abundantly about life, more than she learned in over sixteen years of formal schooling. Her passions include mothering, teaching fine arts, researching and serving as a parent educator. Many years ago, she traded her nightstand for a bookshelf, which always holds at least a dozen books-in-progress, mostly non-fiction reads that support her fairytale notion of saving the world one person at a time.

  • But I thought big pharma directed health care knew everything about the understanding of physiologically based heath care, and that the FDA actually did their job in protecting the general public?

    The Lucifarian – Attack

    King James Bible
    And the light of a candle shall shine no more at all in thee; and the voice of the bridegroom and of the bride shall be heard no more at all in thee: for thy merchants were the great men of the earth; for by thy sorceries were all nations deceived.

    King James Bible
    And the merchants of the earth shall weep and mourn over her; for no man buyeth their merchandise any more:

    Revelation 18: 23, “By Thy Sorceries Were All Nations Deceived.”

    Western Medicine is Rockefeller Medicine – All The Way




    While drug companies profit billions, people are dying by the millions.

    MEDICINE KILLS MILLIONS (direct data and statistics)

    Conventional Medicine is the Leading Cause of Death

    Benjamin Rush
    U.S. Founding Father, Signer of The Declaration of Independence

    Unless we put medical freedom into the Constitution, the time will come when medicine will organize into an undercover dictatorship to restrict the art of healing to one class of Men and deny equal privileges to others; the Constitution of the Republic should make a Special privilege for medical freedoms as well as religious freedom.

    Dr. Benjamin Rush warned about loss of medical freedom over 200 years ago

    Generation SICK: The Power, Politics and Propaganda Behind America’s Health Crisis Paperback – January 10, 2016
    by Dr. Vic Naumov (Author)


    We will use soft metals, aging accelerators and sedatives in food and water, also in the air.

    They will be blanketed by poisons everywhere they turn. The soft metals will cause them to lose their minds. We will promise to find a cure from our many fronts, yet we will feed them more poison.

    The poisons will be absorbed trough their skin and mouths, they will destroy their minds and reproductive systems. From all this, their children will be born dead, and we will conceal this information.

    The poisons will be hidden in everything that surrounds them, in what they drink, eat, breathe and wear. We must be ingenious in dispensing the poisons for they can see far.

    We will teach them that the poisons are good, with fun images and musical tones.

    Those they look up to will help. We will enlist them to push our poisons.

    They will see our products being used in film and will grow accustomed to them and will never know their true effect.

    When they give birth we will inject poisons into the blood of their children and convince them its for their help. We will start early on, when their minds are young, we will target their children with what children love most, sweet things.

    When their teeth decay we will fill them with metals that will kill their mind and steal their future.

    When their ability to learn has been affected, we will create medicine that will make them sicker and cause other diseases for which we will create yet more medicine. We will render them docile and weak before us by our power. They will grow depressed, slow and obese, and when they come to us for help, we will give them more poison.

    John Shockley

    Let me explain something to you all:

    WI-38 is the cell lines from a FEMALE aborted fetus, used to cultivate viruses used in vaccines. When you inject the DNA from a FEMALE (carrying two X chromosomes) into a MALE (who already carries one X chromosome and a weaker Y chromosome) you now have an overload of the X chromosome. Now we have an onslaught of BOYS who think they should be GIRLS.

    Do we have male DNA in vaccines? YES! The MRC-5 is the code given to the fetal cell line also used to cultivate vaccine viral components, and it comes from a MALE aborted fetus. Do we have girls thinking they are boys? YES! Is it as prominent as boys wanting to be girls? NO!

    Why? Because girls have two dominant X chromosomes. When they are injected with a vaccine containing MRC-5, they aren’t just getting a Y chromosome, but yet another dominant X chromosome, on top of the two they already have. That’s why you don’t see as many girls wanting to be boys as you do the other way around.

    The Baphomet is half-male, half-female, blurring the lines. He is in charge of those who are mandating vaccines…they either kill, maim, or confuse our society. Nothing afflicting our children is their fault. It’s all damage from a spiritual battle that we are losing.

    Terri Lewis

    New Published Italian Study: MICRO and NANO-CONTAMINATION in VACCINES

    Chemical Gender Manipulation: Turning boys into girls. Warning: This article is not politically correct

    How many parents know that vaccines have been made using aborted fetal cells, which are more like stem cells, and that in the creation of vaccine antigens. Do you think there is any problem in, and with that? It is again all proven with the pharma clinical trials and previously done scientific studies to be entirely safe and effective; and so you would suppose and expect; right? The fact is that none of it has been tested for safety, and obviously they have not tested even as much as if or not serious levels of DNA residual fragments contamination exist in those vaccines. They simply lie to the public at the CDC and with unproven false assurances, and which are made by what are clearly, falsely assumed authorities.

    Dr Theresa Deisher – Worldwide Autism Epidemic & Human Fetal Manufactured Contaminated Vaccines



    Amazing JFK Speech! He Tells you The Truth!

    This video shows you from the word’s of JFK himself that there is a force working right now to conceal the truth and that we are resting on a delicate balance in not only this country but the WORLD! DURING THIS SPEECH HE TELLS YOU HE IS NOT GOING TO KEEP ANYMORE SECRETS FROM THE WORLD! THEN WHAT HAPPENS LATER? HE GETS SHOT IN THE HEAD! The second half of the video shows other presidents and congressman showing their true colors in regards to strange secrecy!

    Polysorbate 80: A Risky Vaccine Ingredient

    Why wasn’t this important study in any of pharma journal, or the study ever addressed at the CDC?

    Food Chem Toxicol. 1993 Mar;31(3):183-90.
    Delayed effects of neonatal exposure to Tween 80 on female reproductive organs in rats.

    Gajdová M1, Jakubovsky J, Války J.

    Neonatal female rats were injected ip (0.1 ml/rat) with Tween 80 in 1, 5 or 10% aqueous solution on days 4-7 after birth. Treatment with Tween 80 accelerated maturation, prolonged the oestrus cycle, and induced persistent vaginal oestrus. The relative weight of the uterus and ovaries was decreased relative to the untreated controls. Squamous cell metaplasia of the epithelial lining of the uterus and cytological changes in the uterus were indicative of chronic oestrogenic stimulation. Ovaries were without corpora lutea, and had degenerative follicles.

    Concerns on Using Polysorbate 80 in Vaccines


    Here’s a strange one –

    A patent for a vaccine that would decrease the ability for fertility in animals (which can be found here -submitted by the University
    of Georgia Research Foundation) “preferably includes Tween 80 (Polysobate 80)”. [3]

    The patent immediately goes on to site the book “The Theory and Practical Application of Adjuvants” after declaring Tween 80 as a preferable ingredient. This book lists the benefits and pitfalls associated with the use of different adjuvants. Studies include such problems as isolation, adverse reactions and practical applications.[3][4]

    At least there is a practical application for it – decreasing fertility?!

    Read more:




    Polysorbate 80 is a chemical used by physicians to open the blood-brain barrier, for the purpose of chemotherapy for brain cancer. The chemicals then bind tightly to the polysorbate 80 and the chemo can reach the cancer cells.

    Polysorbate 80 is used in vaccines to reduce the surface tension of the chemicals, and increase the solubility of chemicals that normally would not be able to dissolve together (think oil and water). It also works as an emulsifier so the chemicals can disperse evenly upon injection. This sounds like a smart plan, right? The problem is, it also opens the blood-brain barrier and the brain is exposed to the chemicals like aluminum (a neurotoxin), formaldehyde (embalming fluid and a carcinogen), glyphosate (another carcinogen), etc. Since it increases solubility and absorbability, it makes it incredibly easy for the brain to absorb the toxins; the toxins bind tightly to the polysorbate 80 and flow right through the blood-brain barrier to do their damage.
    So sure, you might eat more formaldehyde in pears than you may receive through a shot – but when you’re digesting a pear, your brain isn’t being exposed to formaldehyde in its full *synthetic* form and being damaged by the toxicity; it’s being broken down in its *natural* form by your digestive system, which is equipped to handle it. Injection is very different from ingestion.

    Credit: Allison Claire

    Nanotechnology approaches to crossing the blood-brain barrier and drug delivery to the CNS
    Gabriel A SilvaEmail author

    Applications to drugs and other molecules

    In another example, various compounds – including neuropeptides such as enkephalins, the N-methyl-D-aspartate receptor antagonist MRZ 2/576, and the chemotherapeutic drug doxorubicin – have been attached to the surface of poly(butylcyanoacrylate) nanoparticles coated with polysorbate 80 [3, 4, 5, 6, 7]. The polysorbate on the surface of the nanoparticles adsorb apolipoproteins B and E and are taken up by brain capillary endothelial cells via receptor-mediated endocytosis. Nanoparticle-mediated delivery of doxorubicin is being explored in a rodent model of glioblastoma [3, 8]. Importantly, recent work in a rat glioblastoma model revealed significant remission with minimal toxicity, setting the stage for potential clinical trials [8].

    Read much more:

    Big Pharma’s Dirty Little Secret: Vaccine-Induced Autoimmune Injury

    Nanoparticles enhance brain delivery of blood–brain barrier-impermeable probes for in vivo optical and magnetic resonance imaging

    Several imaging modalities are suitable for in vivo molecular neuroimaging, but the blood–brain barrier (BBB) limits their utility by preventing brain delivery of most targeted molecular probes. We prepared biodegradable nanocarrier systems made up of poly(n-butyl cyanoacrylate) dextran polymers coated with polysorbate 80 (PBCA nanoparticles) to deliver BBB-impermeable molecular imaging probes into the brain for targeted molecular neuroimaging. We demonstrate that PBCA nanoparticles allow in vivo targeting of BBB-impermeable contrast agents and staining reagents for electron microscopy, optical imaging (multiphoton), and whole brain magnetic resonance imaging (MRI), facilitating molecular studies ranging from individual synapses to the entire brain. PBCA nanoparticles can deliver BBB-impermeable targeted fluorophores of a wide range of sizes: from 500-Da targeted polar molecules to 150,000-Da tagged immunoglobulins into the brain of living mice. The utility of this approach is demonstrated by (i) development of a “Nissl stain” contrast agent for cellular imaging, (ii) visualization of amyloid plaques in vivo in a mouse model of Alzheimer’s disease using (traditionally) non–BBB-permeable reagents that detect plaques, and (iii) delivery of gadolinium-based contrast agents into the brain of mice for in vivo whole brain MRI. Four-dimensional real-time two-photon and MR imaging reveal that brain penetration of PBCA nanoparticles occurs rapidly with a time constant of ∼18 min. PBCA nanoparticles do not induce nonspecific BBB disruption, but collaborate with plasma apolipoprotein E to facilitate BBB crossing. Collectively, these findings highlight the potential of using biodegradable nanocarrier systems to deliver BBB-impermeable targeted molecular probes into the brain for diagnostic neuroimaging.

    Polysorbate 80: A Risky Vaccine Ingredient

    (Highlights from the article).

    According to the Material Safety and Data Sheet (MSDS) on, Polysorbate 80 was tested for inhalation and ingestion and demonstrated to be slightly hazardous in case of skin contact.6 The MSDS does not address the effects of polysorbate through injection. Nevertheless, in the same toxicology section under special remarks on chronic and toxic effects on human, it states that Polysorbate 80:

    May cause adverse reproductive effects based on animal test data. No human data found. May cause cancer based on animal test data. No human data found. May affect genetic material (mutagenic). Ingestion of very large doses may cause abdominal spasms and diarrhea. Animal studies have shown it to cause cardiac changes, changes in behavior (altered sleep time) and weight loss (upon repeated or prolonged ingestion). However, no similar human data has been reported.6
    The fact that Polysorbate 80 “may cause cancer based on animal test data” and may be mutagenic alone should be enough to require vaccine manufacturers and the Food and Drug Administration to provide credible scientific evidence that it is safe to include Polysorbate 80 in vaccines given to humans.

    Polysorbate 80: Damage to the Brain?

    In vaccines, Polysorbate 80 acts as an emulsifier to disperse all the other ingredients evenly within the liquid. Pediatrician Lawrence Palevsky, MD warns of the potential danger of using Polysorbate 80 as a vaccine ingredient.8He notes,

    Polysorbate 80 is used in pharmacology to assist in the delivery of certain drugs or chemotherapeutic agents across the blood-brain-barrier.8
    This raises serious concerns of using Polysorbate 80 in combination with other reactive vaccine ingredients, which have the potential to damage the brain.8

    The blood-brain-barrier is a barrier that separates the brain from the circulatory system and protects the central nervous system from harmful chemicals and other toxins. The blood brain barrier is particularly weak and more easily penetrated during infancy and in old age. Consequently, the concern with using Polysorbate 80 in vaccines is that it may permit the entry of other toxic ingredients, such as heavy metals, into the brain.2

    Dr. Palevsky asks some crucial questions regarding whether Polysorbate 80 is having negative effects on and facilitating toxic insults to the brain via vaccination.

    What viral, bacterial, yeast, heavy metal or other vaccine containing ingredient needs to pass into the brains of our children? Do they belong in the brain? Is that part of the needed immune response to protect our children from disease? Do vaccine materials pass across the blood-brain barrier with the help of Polysorbate-80? If so, are there complications from being in the brains of our children?8

    Furthermore, once injected into the body, polysorbate 80 can rapidly break down into sorbitol and ethylene oxide. Sorbitol has the ability to increase the risk of diabetes, cell death, mitochondrial failure and DNA fragmentation.2

    Polysorbate 80: Damage to Uterus?

    Research has demonstrated that Polysorbate 80 can lead to infertility in rats. A study published in the Journal of Food and Chemical Toxicology…

    discovered that Tween80 accelerated the rats’ maturation, prolonged the estrous cycle, decreased the weight of the uterus and ovaries, and caused damage to the lining of the uterus indicative of chronic estrogenic stimulation. The rats’ ovaries were also damaged, with degenerative follicles and no corpora lutea (a mass of progesterone-secreting endocrine tissue that forms immediately after ovulation). Such severe deformities to the ovary can lead to infertility.10

    Polysorbate 80: Damage to Immune Function?

    There are also concerns with the use of detergents in vaccines. Our body has something called the Membrane Attack Complex (MAC)—one of the immune system’s toughest weapons.2 When the body identifies a pathogen, MAC proteins kill the cells of pathogens by tunneling through their surface membranes thus causing them to leak or explode.

    Although there are similarities between MAC proteins and detergents in terms of their “attacking” function, detergents are not regulated in body in the same manner as MAC proteins.2 A protein known as CD59 regulates MAC; its role is to restrain other MAC proteins from attaching to our cells thus preventing them from rupturing.2

    Due to the lack to regulating proteins in detergents, they attack cells randomly and have the potential to attack our own cells ignoring immune system alerts to cease attacking.2

    Several studies illustrate that lack of CD59 protection can lead to damaged neuromuscular transmission junctions, rheumatoid arthritis, kidney disease, stroke or fatal cerebral hemorrhage. Considering that regulatory CD59 protein is non-existent in injected detergents, all of the mentioned medical conditions are to be expected when using detergents in vaccines since they have no regard for other cells that would otherwise be protected by CD59 or other regulating proteins.2

    Verdict on Polysorbate 80

    It is obvious that there is a glaring lack of basic science research into the toxic effects of the vaccine ingredient, Polysorbate 80, on human health. Some argue that ingredients like Polysorbate 80 in vaccines are safe and not dangerous simply because they are present in vaccines in miniscule amounts.

    However, the fact remains that the federal vaccine schedule directs doctors to give infants and children a whopping 49 doses of vaccines by the age of six.11 What are the cumulative effects of multiple vaccine ingredients on the human body? Shouldn’t we have the right to ask for evidence of short and long-term safety if we are going to inject something into our bodies or our child’s body?

    Read more.

    Why wasn’t this important study in any of pharma journal, or the study ever addressed at the CDC?

    Food Chem Toxicol. 1993 Mar;31(3):183-90.
    Delayed effects of neonatal exposure to Tween 80 on female reproductive organs in rats.

    Gajdová M1, Jakubovsky J, Války J.

    Neonatal female rats were injected ip (0.1 ml/rat) with Tween 80 in 1, 5 or 10% aqueous solution on days 4-7 after birth. Treatment with Tween 80 accelerated maturation, prolonged the oestrus cycle, and induced persistent vaginal oestrus. The relative weight of the uterus and ovaries was decreased relative to the untreated controls. Squamous cell metaplasia of the epithelial lining of the uterus and cytological changes in the uterus were indicative of chronic oestrogenic stimulation. Ovaries were without corpora lutea, and had degenerative follicles.

    Concerns on Using Polysorbate 80 in Vaccines


    Here’s a strange one –

    A patent for a vaccine that would decrease the ability for fertility in animals (which can be found here -submitted by the University
    of Georgia Research Foundation) “preferably includes Tween 80 (Polysobate 80)”. [3]

    The patent immediately goes on to site the book “The Theory and Practical Application of Adjuvants” after declaring Tween 80 as a preferable ingredient. This book lists the benefits and pitfalls associated with the use of different adjuvants. Studies include such problems as isolation, adverse reactions and practical applications.[3][4]

    At least there is a practical application for it – decreasing fertility?!

    Read more:


    Brief Description of the Drawings

    In a preferred embodiment the vaccine comprises oil, preferably a biodegradable oil such as squalene oil, in an amount of about 2.5% to about 15%, preferably about 8% to about 12%. In preparing the vaccine it is advantageous to combine a concentrated oily adjuvant composition with an aqueous solution of the antigen, pZP glycoprotein. Typically, the vaccine is prepared using an adjuvant concentrate which contains lecithin (about 5% to about 15 % wt/vol, preferably about 12% wt /vol) and STDCM (preferably about 25 mg/mL to about 50 mg mL) in squalene oil. The term % wt/vol means grams per 100 mL of liquid. The aqueous solution containing the isolated pZP glycoprotein is typically a phosphate-buffered saline (PBS) solution, and additionally preferably contains Tween 80 (about 0.2% vol/vol to about 0.8% vol/vol, preferably about 0.4% vol/vol). See J.A. Rudbach et al., “Ribi

    The animal is given an initial dose, usually via intramuscular injection although subcutaneous injection can also be used. The initial injection is followed by two or more booster injections at two to four week intervals, although the boosters can be administered from about 9 days to about twelve months following the previous vaccination. The body’s immunological response to the vaccine at this dosing regimen appears to render the ovaries permanently inactive as a result of, for example, follicle disruption or destruction, as evidenced by
    immunocytochemical analysis and histological evaluation of the ovarian tissue of vaccinated subjects. Sterility is permanent and irreversible. Immunosterilization of carnivores in accordance with the present method typically does not cause abnormal estrus cycles or other significant undesirable side effects in the vaccinated subjects.

    When the vaccine is administered to a dog or a cat as described above, but with only one booster instead of two or more boosters, the vaccine typically results in immunocontraception (i.e., temporary or transient, reversible infertility) rather than immunosterilization.;jsessionid=8A5562CE40BFFA234201ABC59BBCC805.wapp2nA?docId=WO1999034825&recNum=1&maxRec=&office=&prevFilter=&sortOption=&queryString=&tab=PCTDescription

    Polysorbate 80 is used in clinical trials and the development of cancer and other drugs that need to cross the BBB more easily, and to get that drug into the brain.

    An example of one of those studies.

    Pharm Res. 1999 Oct;16(10):1564-9.
    Significant transport of doxorubicin into the brain with polysorbate 80-coated nanoparticles.
    Gulyaev AE1, Gelperina SE, Skidan IN, Antropov AS, Kivman GY, Kreuter J.

    The present study demonstrates that the brain concentration of systemically administered doxorubicin can be enhanced over 60-fold by binding to biodegradable poly(butyl cyanoacrylate) nanoparticles, overcoated with the nonionic surfactant polysorbate 80. It is highly probable that coated particles reached the brain intact and released the drug after endocytosis by the brain blood vessel endothelial cells.

    Additionally we have the new finding in a study coming out of Italy and which shows as well concerning levels of various toxic metals that have been found in several of the childhood vaccines, as contaminants. How would such contamination get into childhood vaccines? That, unless it was done deliberately. And why is the FDA and CDC not responding to that seriously revealing study?

    New Published Italian Study: MICRO and NANO-CONTAMINATION in VACCINES

    New Quality-Control Investigations on Vaccines: Microand

    Vaccines are being under investigation for the possible side effects they can cause. In order to supply new information, an electron-microscopy investigation method was applied to the study of vaccines, aimed at verifying the presence of solid contaminants by means of an Environmental Scanning Electron Microscope equipped with an X-ray microprobe. The results of this new investigation show the presence of micro- and nanosized particulate matter composed of inorganic elements in vaccines’ samples which is not declared among the components and whose unduly presence is, for the time being, inexplicable. A considerable part of those particulate contaminants have already been verified in other matrices and reported in literature as non biodegradable and non biocompatible. The evidence collected is suggestive of some hypotheses correlated to diseases that are mentioned and briefly discussed.

    Read more:

    Non-linear dose-response of aluminium hydroxide adjuvant particles: Selective low dose neurotoxicity. Crépeaux G, et al. Toxicology. 2017.

    Slow CCL2-dependent translocation of biopersistent particles from muscle to brain

    More problems with aluminum adjuvants.

    Influence of elemental impurities in aluminum hydroxide adjuvant on the stability of inactivated Japanese Encephalitis vaccine, IXIARO®

    Aluminum hydroxide is a critical raw material in the production of many vaccines. It is used as an adjuvant in the formulation of the final bulk vaccine, and for this it must meet the specifications of the European Pharmacopeia Monograph. We investigated whether vaccine stability was affected by the presence of trace amounts of elemental impurities in commercially available aluminum hydroxide. The content of residual elemental impurities in commercially available aluminum hydroxide was determined by selective and sensitive inductively coupled-plasma mass spectrometry and inductively coupled plasma atomic emission spectroscopy. We found significant differences between different suppliers, but also between different lots from the same supplier. Inactivated Japanese encephalitis vaccine, IXIARO®, was used to study the effect of residual metals in aluminum hydroxide on antigen stability. We propose that antigen degradation occurred via a pathway involving the metal-catalyzed, auto-oxidation of a process-related impurity (sulfite). Thus, sulfite auto-oxidation resulted in antigen degradation when residual Cu was present at elevated concentrations in aluminum hydroxide.

    When you read this study below you can obviously envision the high risk it would be to as well add polysorbate 80 to a vaccine, and/or among the mix of other vaccines a child is given in a single day and office visit.

    Neurosci Biobehav Rev. 1989 Spring;13(1):47-53.
    Aluminum-induced neurotoxicity: alterations in membrane function at the blood-brain barrier.
    Banks WA1, Kastin AJ.

    Aluminum is established as a neurotoxin, although the basis for its toxicity is unknown. It recently has been shown to alter the function of the blood-brain barrier (BBB), which regulates exchanges between the central nervous system (CNS) and peripheral circulation. The BBB owes its unique properties to the integrity of the cell membranes that comprise it. Aluminum affects some of the membrane-like functions of the BBB. It increases the rate of transmembrane diffusion and selectively changes saturable transport systems without disrupting the integrity of the membranes or altering CNS hemodynamics. Such alterations in the access to the brain of nutrients, hormones, toxins, and drugs could be the basis of CNS dysfunction. Aluminum is capable of altering membrane function at the BBB; many of its effects on the CNS as well as peripheral tissues can be explained by its actions as a membrane toxin.

    And again, what happens when was well combine vaccine aluminum adjuvants with all this?

    Amount of aluminum adjuavnt in vaccines per dose

    Pneumococcal vaccine 0.125 mg
    • Diphtheria-tetanus-pertussis (DTaP) vaccine– 0.17-0.625 mg
    • Haemophilus influenzae type b (Hib) vaccine– 0.225 mg
    • Hib/Hep B vaccine 0.225 mg
    • Hep A vaccine (for children) 0.225-0.25 mg
    • Hepatitis B vaccine (Hep B) 0.225-0.5 mg
    • Hep A/ Hep B vaccine 0.45 mg
    • DTaP/inactivated polio/ Hep B vaccine 0.85 mg
    • DTaP/inactivated polio/Hib vaccine 0.33 mg
    • Human Papillomavirus (HPV) vaccine 0.225 mg-0.500 mg

    Vaccine Ingredients: America’s Dirty Little Secret

    Toxins in vaccines infiltrate the brain

    What happens to children when they receive aluminum containing vaccines?

    Immunol Res. 2013 Jul;56(2-3):304-16. doi: 10.1007/s12026-013-8403-1.
    Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity.
    Shaw CA1, Tomljenovic L.

    We have examined the neurotoxicity of aluminum in humans and animals under various conditions, following different routes of administration, and provide an overview of the various associated disease states. The literature demonstrates clearly negative impacts of aluminum on the nervous system across the age span. In adults, aluminum exposure can lead to apparently age-related neurological deficits resembling Alzheimer’s and has been linked to this disease and to the Guamanian variant, ALS-PDC. Similar outcomes have been found in animal models. In addition, injection of aluminum adjuvants in an attempt to model Gulf War syndrome and associated neurological deficits leads to an ALS phenotype in young male mice. In young children, a highly significant correlation exists between the number of pediatric aluminum-adjuvanted vaccines administered and the rate of autism spectrum disorders. Many of the features of aluminum-induced neurotoxicity may arise, in part, from autoimmune reactions, as part of the ASIA syndrome.

    Scientists in Canada Being Censored from Covering Dangers of Aluminum in Vaccines

    Christina England writes about vaccine censorship in Canada and the involvement of the World Health Organization. This is an especially crucial topic, as recent studies show just how toxic and dangerous aluminum adjuvants in vaccines are, and the public has a right to have access to this information from scientists in Canada.

    Canadian Media and the WHO Attempt to Discredit Scientists from University of British Columbia

    by Christina England
    Health Impact News

    When a professional gets a little too close to the truth for comfort, the most efficient and effective way for government agencies and the pharmaceutical industry to prevent them from exposing the truth is to destroy their credibility.

    This is exactly what happened when Professor Shaw and Dr. Tomljenovic published a series of leading papers exposing the possible links between aluminum adjuvants and autism.

    The question is, what exactly is being covered up and why?

    Canadian Media are Involved in the Attack, but Exactly WHO are They Working For?

    What Had Professor Shaw and Dr. Tomljenovic Discovered and Why Had it Been Covered Up?

    Read more:

    228 Abstracts with Vaccine Adjuvants Research

  • Health does NOT come from the end of a toxic and known contaminated vaccine syringe and needle. Wake up.

    Master Manipulator: The Explosive True Story of Fraud, Embezzlement, and Government Betrayal at the CDC


    But you never seen any of this in the US major media, did you? There is an organized effort not only in the US, but globally, to mandate vaccines. The desperation is at an all time high to gain control and to continue to lock in their vaccine profits, save their careers, and with no accountability and nor legal liability existing, they still get away with denying what they have done.

    Thousands of Citizens Rise up Against Mandatory Vaccines in Italy Italians protest new vaccination laws – mainstream media blackout