Category Archives: Eugenocide/Population Control

Refusing to be silent: Parents’ stories on how their children died from vaccines

From: Amber Powers – CPS Threatened to take my twins at birth – shortly after being pressured to receive Tdap and Flu vaccine both twins died before birth.

From: Isabelle Stevens – Two of my children suffered severe neurological injuries, seizures, posturing and ultimately died five days after vaccination in 2012

From: Jessica Taylor – Doctor said his death was a side effect of one of the many vaccines he received that day but said he can’t go on record stating it was because of the vaccines

From: Brandi Nolan – unborn baby died after flu shot

READ Stories …

MAD IN AMERICA: Electroshock therapy for children….a mad story

Electroshocking Children-Why It Should Be Stopped

John Breeding

In 1947, psychiatrist Lauretta Bender.…In 1955, she reported on how she had administered 20 shock treatments to a child under three years old, who was on the children’s ward at New York’s Bellevue Hospital.(3)  Bender eventually administered this “treatment” to more than 500 children, and enjoyed a career as one of the most honored psychiatrists of her time. She is still on the govt. payroll today and exalted as a leading psychiatrist of our time.

One of the children she shocked was Ted Chabasinski, when he was a six-year-old foster child. His description of that experience stands in stark contrast to Bender’s:

I was six years old [in 1944]. My mother had been locked up in a mental hospital just before I was born, and I was a ward of the state. A psychiatrist at Bellevue Hospital in New York, Dr. Lauretta Bender, had just begun her infamous series of experiments with shock treatment on children, and she needed more subjects. So I was diagnosed as a “childhood schizophrenic,” torn away from my foster parents, and given 20 shock treatments….18 I was dragged down the hallway crying, a handkerchief stuffed in my mouth so I wouldn’t bite off my tongue. And I woke [after the shock treatment] not knowing where I was or who I was, but feeling as if I had undergone the experience of death. After four months of this. I was returned to my foster home. Shock treatment had changed me from a shy little boy who liked to sit in a corner and read to a terrified child who would only cling to his foster mother and cry. I couldn’t remember my teachers. I couldn’t remember the little boy I was told had been my best friend. I couldn’t even find my way around my own neighborhood. The social worker who visited every month told my foster parents that my memory loss was a symptom of my mental illness. A few months later, I was shipped to a state hospital to spend the next 10 years of my life.

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ALERT for humanity: The “perfect storm” for a vaccine HOLOCAUST is now here!

No one is allowed to criticize vaccines. No whistleblowers are covered in the media. No investigative findings can be shared on social media. The cover-up is now complete, and the vaccine industry answers to no one, but hopes to violate everyone.

Mass death has now descended upon us, and it’s all being carried out in the name of “science.”
READ MORE…

Transgender girl….adorable…and so smart

This short film is certainly a testimony of the reality of a physiological boy who identifies as a girl in this Christian family.

VLA Comment:

Transgender identity; homosexuality, in many observations, is a result of toxic agriculture causing hormonal disruption in the growing fetus. In Italy and Greece, it was the metal lead, as a hormonal disruptor, in the plumbing of the rich that caused the wave of homosexuality in those countries. Documented extensively by the late Peter Montague of Rachel’s Hazzardous newsletter, homosexuality and now the advanced burden of gender dysphoria has its roots in toxic agriculture. Virtually no one is looking to the Cause.

Parkinson Disease-Impending pandemic

Emerging evidence of an impending Parkinson’s disease pandemic identified

Neurological disorders are now the leading cause of disability globally, and the fastest growing neurological disorder in the world is PD, a slowly progressive disorder that affects movement, muscle control, and balance. In 1855, forty years after Dr. James Parkinson first described the condition, approximately 22 people of 15 million in England and Wales died of PD. In 2014, roughly 5,000 to 10,000 individuals of 65 million in the UK died of PD. From 1990 to 2015, the number of people with PD doubled worldwide to over six million. Driven principally by aging, this number is projected to double again to over 12 million by 2040, and additional factors, including increasing longevity, declining smoking rates, ….VLA Comment: How about mass vaccination for nearly every newborn, toddler, child and adolescent….that presents in the majority of the emerging generation neurological and physiological disorders and regressions.

Posted on Jul 4, 2019 in Chronic Disease, Medical Rewind

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Terraforming the Earth: Mike Adams

Mike Adams (NATURAL NEWS/THE HEALTH RANGER) discusses terraforming the planet as to make earth inhabitable to an alien species. He will be live in Branson, Missouri, Sept 13-15 for the True Legend Conference with Steve Quayle of which I (VLA founder) intend to go.I am a fan of both Mike Adams and Steve Quayle.

I have also included herein the Lecture of Dr. Rudolf Steiner, Christian Clairvoyant and founder of Biodynamic Agriculture, the Waldorf education system and Anthroposophy called the 8th (demonic) sphere. Included in this link is the alert on 5G that appears to be part of plan.

Glyphosate (Monsanto’s (now Bayer) Round UP) Contaminated Vaccines

In our most recent article, “Glyphosate Pathways to Modern Diseases VI: Prions, Amyloidoses and Autoimmune Neurological Diseases,” we present evidence that glyphosate has made its way into several widely used vaccines. We describe how the glyphosate residue contained in vaccines might induce the kind of autoimmune responses typically observed in autism.
 
Interestingly, of all the vaccines we tested, MMR stood out as consistently having the highest level of glyphosate contamination. This fact may help explain why the MMR vaccine, which contains neither mercury nor aluminum, has been implicated so often in vaccine injury and autism.

How Might Glyphosate Make Its Way into Vaccines?

Vaccines can become contaminated in many ways. One potential source of contamination is the animal tissue (chicken embryo, fetal bovine serum, monkey kidney, etc.) that is used as a culture medium to grow the viruses contained in vaccines. The measles virus for the MMR is grown on gelatin made from the bones and ligaments of commercially raised cows and pigs, animals that have been fed a steady diet of Roundup Ready corn and soy feed. Gelatin is also used as a stabilizer in vaccines, creating another possible route of contamination.
 
As Roundup producer Monsanto itself has reported, the residue from glyphosate tends to accumulate in the bones, marrow, and collagen-rich ligaments of animals. Anthony Samsel confirmed this finding in his own study of the bones, marrow, and other parts of pigs and cows, as well as the derived bovine gelatin.
 
To provide additional evidence that gelatin is the source of glyphosate contamination in vaccines, Samsel looked at a number of gelatin-based products, including Jell-O, gummi vitamins, and protein powders. He also looked at digestive enzymes such as trypsin and lipase. He found significant glyphosate residue in all of them.
 
It should come as no surprise, then, that all of the vaccines that list gelatin and bovine serum as ingredients tested positive for glyphosate, while those that contained neither of these ingredients tested negative.
 
Roundup-pic-1
 
Glyphosate may be contributing to another source of vaccine contamination. In a recent study published in the International Journal of Vaccines and Vaccination, researchers were shocked to discover a variety of toxic metals in a number of common vaccines Platinum, silver, bismuth, iron, and chromium all showed up in the MMR vaccine.
 
The source of these contaminants is considered to be a mystery. It is interesting to note in this context that glyphosate was first patented as a pipe cleaner due to its remarkable ability to chelate metals It may be the case that glyphosate is playing a role in extracting metals from containers during the manufacture of vaccines.
 
My research leads me to believe that synergistic toxicity between glyphosate and vaccines, particularly MMR, is a major factor in the growing autism epidemic. The severity of MMR-related adverse events, as reflected in the FDA’s Vaccine Adverse Event Reporting System, has increased steadily in recent years—along with the use of glyphosate on corn and soy crops in the U.S.
Some of the reactions that have become significantly more common after 2002 compared to before 2002 are seizures, anaphylactic shock, asthma, autism, eczema, irregular heart rate, and ear infection. Of course, correlation does not prove causation; it is important to understand how glyphosate residues might disrupt the body’s immune system.
 

How Might the Glyphosate in Vaccines Cause Autism?

In our recent article, Samsel and I describe how the measles virus in the MMR, which is grown on nutrients contaminated with glyphosate, could incorporate this glyphosate into its own proteins, as a coding error, in place of the amino acid glycine. Glyphosate is a glycine molecule with an additional methyl phosphonyl group attached to the nitrogen atom, and we have argued that a key mechanism of its insidious cumulative toxicity is its ability to substitute for glycine by mistake during protein synthesis.
 
Haemagglutinin is the main antigen produced by the measles virus that is responsible for inducing an antibody response to the vaccine. A glyphosate-contaminated haemagglutinin molecule from a measles virus will be much more allergenic than one that is free of glyphosate.
 
When the measles virus from the vaccine gains access to the brain, the brain’s immune system acquires antibodies to this abnormal haemagglutinin molecule, and then, through molecular mimicry, these antibodies become autoantibodies to myelin basic protein, a basic component of the myelin sheath. This autoimmune attack on the nerve fibers in the brain disrupts neuronal communication channels, causing the symptoms of autism.
 
Vijendra K. Singh and his colleagues at Utah State University have published multiple papers, dating back to the 1990s, proposing that an autoimmune attack on the myelin sheath due to a viral infection may be a causative factor in autism. In their 2002 paper, “Abnormal Measles-Mumps-Rubella Antibodies and CNS Autoimmunity in Children with Autism,” they concluded that “an inappropriate antibody response to MMR, specifically the measles component thereof, might be related to pathogenesis of autism.”
 
A paper published by Dr. William Shaw in 2017 discussed a set of triplets—two boys with autism and a girl with a seizure disorder—all of whom had high levels of glyphosate in their urine and a disrupted gut microbiome, which he proposed was a causative factor.
 

Gut Dysbiosis: a Primary Factor

Not all children will respond to a glyphosate-contaminated vaccine in the same way A key factor that increases susceptibility of the brain to damage is an unhealthy gut microbiome, which leads to a leaky gut barrier and subsequently a leaky brain barrier, via a tight communication channel between the gut microbes and the brain.
 
Prior chronic exposure to high levels of dietary glyphosate can set a child up for a severe adverse reaction to a vaccine. Dr. Andrew Wakefield, together with many colleagues, published a seminal article in the Lancet in 1998 on a case study of twelve children, all of whom had a gut disorder and all of whom suffered onset of gastrointestinal and neurological symptoms following MMR vaccine, with regression into an autism-like syndrome.” Parents of eight of the children cited MMR as the trigger for their child’s decline.
 
Wakefield was among the first scientists to recognize the important role of a disrupted gut microbiome in the etiology of autism. Unfortunately, the Lancet paper was later retracted and other researchers were very slow to follow up on this important lead, although finally today an unhealthy gut is recognized as a key feature linked to autism.
 
Dr. Wakefield recognized that the children in his study suffered from a leaky gut barrier, as a consequence of damage to the lining of the small intestine. This lining is covered with millions of small projections called villi, creating a huge surface area for the absorption of nutrients.
 
The cells that form these villi, called enterocytes, begin life as an undifferentiated stem cell in the “crypt” area of the intestines. From there, they proliferate and mature as they migrate up the walls of the crypt, and then settle in on the surface of the villi, where they absorb nutrients before dying and getting replaced by new arrivals in a constant renewal process, as illustrated in Figure 1.
 
Glyphosate, as an amino acid, is actively imported into cells along L-type amino acid transporters. Cells that proliferate, like enterocytes, express high levels of these transporters, and therefore preferentially take up glyphosate.
 
In Celiac disease (gluten intolerance), the enterocytes are destroyed more quickly due to exposure to glyphosate and other toxic chemicals. This damage causes the cells to proliferate more quickly, in order to replace destroyed cells. Increased proliferation causes an increase in the uptake of glyphosate, creating a downward spiral.
 
Thus, glyphosate residue in food sets a child up to fail following an MMR vaccine. Wheat, barley, oats, chick peas, lentils, and sugar cane are not glyphosate resistant, but glyphosate is frequently used as a desiccant or ripening agent for them right before harvest, and it is actively taken up by the seed.
 
Some of the highest levels of glyphosate have been found as a contaminant in these non-GMO foods, so eating “non-GMO” is not adequate for glyphosate avoidance. Glyphosate is not allowed in organic agriculture, so buying USDA certified organic foods is the best option. Children with autism often suffer from gluten intolerance, and I believe glyphosate is a major causative factor in both conditions.
 
2017-8-15-GMO-Villi
Figure 1: Schematic of the enterocytes in the villi lining the walls of the small intestine, which migrate upward from the crypt to the villus as they mature into functioning enterocytes from initial stem cells. These cells are especially vulnerable to glyphosate toxicity, leading to a leaky gut syndrome.
 

A Lost Generation

We have been misled for far too long by the claim that vaccines are “safe and effective.” It is not at all clear that inducing specific antibodies to a small set of infective agents, such as the measles virus, while weakening the immune system’s ability to fight off all the other infective agents in the environment, is the best way to deal with infectious disease.
 
As we have seen, antibodies can become autoantibodies and attack the body’s own tissues, leading to chronic diseases that are often worse than the infectious diseases they protect from.
Vaccinated children suffer from many debilitating neurological and autoimmune diseases in far greater numbers than unvaccinated children. The manufacture of vaccines is a tricky process, and along with the acknowledged toxic ingredients like mercury, aluminum, and formaldehyde, they also have been found to contain contaminants like glyphosate and toxic metals that may well be the biggest contributors to severe adverse reactions.
 
Children today may already be a lost generation, but several policy changes need to take place in the immediate future to save subsequent generations from a similar fate.
 
 
We need to repeal the 1986 legislation that protects pharmaceutical companies from liability when a child’s life is ruined by a vaccine. This will surely pressure them to try harder to keep impurities out of vaccines.
 
We need to eliminate laws such as California’s SB277 that prevents unvaccinated children from enrolling in public or private schools, and be vigilant to ensure other states don’t follow suit. Then parents will be empowered to make decisions about the best path towards building a strong immune system in their child.
 
Part of that program needs to be a switch to a 100 percent USDA certified organic diet, in order to protect children from the dangers posed by toxic herbicides, insecticides and fungicides.
 
Finally, we need to insist that our elected representatives pass laws that protect consumers from products like glyphosate, which are designed to disrupt processes that support life.
 
PUTTING THE PIECES TOGETHER: Exposure to glyphosate may play an important role in the development of autism
.
Top 5 Reasons to Avoid Glyphosate Exposure
 
  1. Glyphosate is a “Probable” Carcinogen
    In March of 2015, scientists at the UN’s International Agency for Research on Cancer (IARC) declared glyphosate a probable human carcinogen. The IARC report linked glyphosate to non-Hodgkin lymphoma in humans and to cancer in laboratory animals, and indicated it can cause “DNA and chromosomal damage in human cells.”
 
  1. Glyphosate is a Patented Antimicrobial Agent
    Glyphosate disrupts the gut microbiome leading to the overgrowth of pathogens and inflammatory bowel disease.
 
3. Glyphosate Negatively Impacts the Brain
According to the National Pesticide Information Center at Oregon State University (NPIC), glyphosate exposure has been linked to developmental effects when administered to pregnant rats in high doses.
 
  1. Glyphosate May Disrupt the Reproductive System
The Western world faces an epidemic in declining sperm quality.  The NPIC links high dose exposure in rats to negative reproductive effect.
 
5. Glyphosate May Be a Critical Factor the Autism Epidemic
Much evidence supports this, including disruption of the gut microbiome, chelation of important minerals like manganese and zinc, and extremely high correlations between time trends in autism and in the use of glyphosate on core crops.
 
 
Dr. Stephanie Seneff is a Senior Research Scientist at MIT’s Computer Science and Artificial Intelligence Laboratory in Cambridge, Massachusetts, USA. She has a BS degree from MIT in biology and MS, EE and PhD degrees from MIT in electrical engineering and computer science.  She has published over 200 peer-reviewed papers in scientific journals and conference proceedings. Her recent interests have focused on the role of toxic chemicals and micronutrient deficiencies in health and disease, with a special emphasis on the pervasive herbicide, Roundup, and the mineral, sulfur.  She has authored over thirty peer-reviewed journal papers over the past few years on these topics, and has delivered numerous slide presentations around the world.
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Vaccines Excipients: PHARMACOGENETICS: Inability of infants and children to metabolize vaccine xenobiotic excipients

Clinical Pharmacogenetics in Pediatric Patients

Anwar Husain; Jennifer A. Loehle; David W. Hein Pharmacogenomics. 2007;8(10):1403-1411.

Newborns and infants rapidly undergo simultaneous stages of organ growth and demonstrate large variability in drug response and metabolizing capabilities.[1,2] The enzymes, transporters and targets important for pediatric drugs all have the potential to vary along developmental timelines in terms of affinity, functional capacity and expression. Drug-metabolizing enzymes can vary according to chronological age.[3,4]

As such, determining gene expression patterns at various ontological periods becomes of key importance in formulating treatment plans for pediatric patients. Exposure to toxins or pharmaceutical agents or lack of medical treatment of a particular illness at sensitive periods of development could irreversibly disrupt the normal maturation of an individual. Observable consequences of such disruption may not appear until much later in life.              READ MORE….

ASTHMA excerpt: Polymorphisms (lack of specific enzyme in individuals) have been identified within the molecular proteins and enzymes involved in the pathways by which such drugs (vaccine excipients) may bring about their effects that may influence inter-individual variation in patient response.

What is Cytochrome P450 and what does it have to do with drugs and vaccine metabolism and adverse reactions?

Cytochrome P-450 is the liver’s enzyme system and is responsible for most drug metabolism.  Numerous medications, nutrients, and herbal therapies are metabolized through the cytochrome P450 (CYP450) enzyme system. This system can be inhibited or induced by drugs including excipients in vaccines. It is to be noted that cytochrome P450 is maturing and is immature in infants who are regularly vaccinated with Hepatitis B as early as one hour and those who receive the Vitamin K injection.

There are more than 50 CYP450 enzymes, but the CYP1A2, CYP2C19, CYP2D6, CYP1A2, CYP3A4, and CYP3A5 enzymes are responsible for metabolizing 45% of drug metabolism. The CYP2D6 (20–30%), the CYP2C9 (10%) and the CYP2E1 and CYP1A2 (5%) complete this enzyme system. Many ingredients in vaccines inhibit Cytochrome P450, therefore the offending agent remains in the body of the infant and toddler and act as a poison damaging the mitachondria found in every cell in the body except for the blood.   If a medication is taken with an agent that inhibits its metabolism, then the toxin level can rise and result in a harmful or adverse effect.

But it is not only that “all” infants  have immature Cyp 450 enzymes.  For example, 10% of Caucasians are non-metabolizers (Cyp 450 2D6).  For their whole life long these poor (polymorphic) metabolizers cannot metabolize 20-30% of drugs.  7% of African Americans are poor/non metabolizers of drugs dependent on CYP2D6.  Due to hereditary genetic variations (not defects) they do not have the activity of Cyp 2D6. That means that children and teens given drugs such as Adderall, Haldol, Respiridal; street drugs like LSD, psilosybn, cocaine, codeine without adequate genetic pre-testing are likely to have “drug induced psychosis”; suicidal ideation, homicidal ideations by which “heinous” thoughts drive them to such violence as school shootings and mass attacks.

  *Ped cyp enzymes  (see graph)  (very important study of the immaturity of cyp 450 superfamilies in infants and children.

STUDY DOWNLOAD

Synopsis:  Infants do not have a mature liver or liver enzyme function such as Cytochrome P450 and its various metabolites until the age of three years old. Hence upwards of 36 vaccine doses by 18 months old containing the above excipients are poisoning the world’s emerging humanity.:

Study #2:  Immaturity of Cyp 450 in Neonate boys (book)

Study #3 (2018) The Ontogeny of Cytochrome P450 Enzyme Activity and Protein Abundance in Conventional Pigs in Support of Preclinical Pediatric Drug Research

Joske Millecam1, Laura De Clerck2, Elisabeth Govaert2, Mathias Devreese1, Elke Gasthuys1, Wim Schelstraete1, Dieter Deforce2, Lies De Bock3, Jan Van Bocxlaer3, Stanislas Sys4 and Siska Croubels1*

Neonate maturation of Cyp 450 Enzymes (table)

Comprehensive Vaccine Ingredient Information- CDC VACCINE EXCIPIENTS LIST PER VACCINE  CDC Vaccine excipients-table-2 

DIRECT LIST OF THE XENOBIOTIC INGREDIENTS IN VACCINES

Medical treatments and drug protocols including vaccines should be  implemented within a framework of the patient’s heritage, race, and culture in order to provide effective management modalities. Infants as well as adults should be assessed for their ability to metabolize the ingredients in vaccines.

When in comes to diet,  CYP450 inducers and inhibitors are commonly ingested items such as grapefruit juice (inhibitor) and tobacco and herbs such as St. John’s Wort (inducers).  In the case of grapefruit juice, there are numerous medications known to interact with grapefruit juice including statins, antiarrhythmic agents, immunosuppressive agents, and calcium channel blockers. Furthermore, the inhibition of the enzyme system seems to be dose dependent; thus, the more a patient drinks, the more the inhibition that occurs. Additionally, the effects can last for several days if grapefruit juice is consumed on a regular basis. Luckily, the effect of this is not seen with other citrus juices.

Hopefully, this brief review has opened the door to your inquisitive nature on how the liver’s enzyme system is effected by numerous medications and vaccine excipients and why some patients experience clinically significant unanticipated adverse reactions or therapeutic failures.

The above was edited and altered to include vaccines excipients from Davis’ Drug Guide

Effects of Polysorbate 80, a widely used ingredient in vaccines

The results indicate that these non-ionic surfactants are in vitro inhibitors of CYP-mediated metabolism and might have the potential to modify the pharmacokinetics of co-administered drugs, which are substrates of CYP, and thereby enhance their bioavailability.

Read more…

More on Polysorbate 80 and Polysorbate 20

The vaccine ingredients effects on the human body, followed by links to substantiating documentation of causation

Comprehensive Vaccine Ingredient Information- CDC VACCINE EXCIPIENTS LIST PER VACCINE  CDC Vaccine excipients-table-2 

Vaccination ingredients according to the product insert:

MMR II: Measles, Mumps and Rubella

http://www.merck.com/product/usa/pi_circulars/m/mmr_ii/mmr_ii_pi.pdf

The Ingredients: measles, mumps, rubella virus, neomycin, sorbitol, hydrolized gelatin, chick embryonic fluid, and human diploid cells from aborted fetal tissue.

Infanrix: Dipthetheria, Tetanus and Pertussis

http://us.gsk.com/products/assets/us_infanrix.pdf

The Ingredients: Diphtheria, Tetanus and Pertussis toxoids, 2-Phenoxyethanol, Aluminum hydroxide, and Formaldehyde.

IPOL: Polio

http://www.vaccineshoppe.com/US_PDF/IPOL_942420_11.06.pdf

The Ingredients: 3 types of polio viruses, neomycin, streptomycin, polymyxin B, formaldehyde, 2-phenoxyethenol, and a continuous line of monkey kidney cells.
Act-Hib: Haeomophilus Influenza type B

http://www.novaccine.com/pdffiles/Act_HIB_package_insert.pdf

The Ingredients: Haemophilus influenza Type B, polyribosylribitol phosphate, ammonium sulfate, formalin, and sucrose.
Menactra: Meningococcal

www.fda.gov/CbER/products/menactra.htm

The Ingredients: Neisseria meningitidis A, C, Y and W-135 strains, Mueller Hinton Agar, Watson Scherp Media, polysaccharide antigens, formaldehyde, diphtheria toxoid protein, ammonium sulfate.
Prevnar: Pneumococcal

http://www.wyeth.com/content/showlabeling.asp?id=134

The Ingredients: saccharides from capsular Streptococcus pneumoniae antigens (7 serotypes) individually conjugated to diphtheria CRM 197 protein, aluminum phosphate, ammonium sulfate, soy protein, and yeast.

Varivax: Varicella (chickenpox)

www.merck.com/product/usa/pi_circulars/v/varivax/varivaxpi.pdf

The Ingredients: varicella live virus, neomycin, phosphate, sucrose, and monosodium glutamate (MSG), processed gelatin, fetal bovine serum, guinea pig embryo cells, albumin from human blood, and human diploid cells from aborted fetal tissue.
Rotarix: Rotavirus

http://www.fda.gov/CbER/label/rotarixLB.pdf

The Ingredients: weakened human rotavirus, dextran, sorbitol, xanthan, Dulbecco’s Modified Eagle Medium (DMEM), which contains: sodium chloride, potassium chloride, magnesium sulphate, ferric (III) nitrate, sodium phosphate, sodium pyruvate, D-glucose, concentrated vitamin solution, L-cystine, L-tyrosine, amino acids solution, L-glutamine, calcium chloride, sodium hydrogenocarbonate, and phenol red.
Gardasil:HPV
http://www.merck.com/product/usa/pi_circulars/g/gardasil/gardasil_pi.pdf
The Ingredients: HPV types 6, 11, 16 and 18, saccharomyces cerevisiae, “fermentation media”, aluminum, sodium chloride, polysorbate 80, sodium borate.
FluZone (or FluShield, same product): Influenza

www.fda.gov/CBER/label/fluzoneLB.pdf

The Ingredients: Trivalent influenza virus, gentamicin sulphate, formaldehyde, thimerosal, polysorbate 80 (Tween 80) and chick embryonic fluid

Havrix: Hepatitis A

http://us.gsk.com/products/assets/us_havrix.pdf

Ingredients: Hepatitis A virus/toxoids, formalin, aluminum hydroxide, 2-phenoxyethanol, polysorbate 20, and residual MRC5 proteins -human diploid cells from aborted fetal tissue.
Energix B: Hepatitis B

http://us.gsk.com/products/assets/us_engerixb.pdf

The Ingredients: genetic sequence of the hepatitis B virus that codes for the surface antigen (HbSAg), cloned into GMO yeast, aluminum hydroxide, and thimerosal.
———————————————————————–

What’s in the vaccine that needs Cyp450 to metabolize?

Comprehensive list of Xenobiotics in Vaccines: MUST SEE LIST

Vaccine Ingredients

Aluminum= Neurotoxin
http://informedcitizensagainstvaccination.blogspot.com/2009/11/aluminum-neurotoxic-vaccine-adjuvant.html

Formaldehyde= Carcinogen (cancer causer); linked causally to an assortment of cancers, most recently Leukemia. The International Agency for Research on Cancer (IARC) classified it as a known human carcinogen in 2004.
http://informedcitizensagainstvaccination.blogspot.com/2009/11/formaldehyde-carcinogen-in-vaccinations.html

Thimerosal (mercury)= Neurotoxin; controversially linked to Autism in the media, but is well known and causally proven to cause many neurological disorders, cell death in the brain, mitochondrial damage, etcetera. Thimerosal is still being used in the Hepatitis B and Influenza vaccines as of 2009, and is also contained within several of the H1N1 vaccinations.

http://informedcitizensagainstvaccination.blogspot.com/2009/11/thimerosal-neurotoxic-in-plethora-of.html
2-Phenoxyethanol aka “Antifreeze” aka “ethylene glycol monomethyl ether”= neurotoxic, CNS toxicant.
http://informedcitizensagainstvaccination.blogspot.com/2009/11/2-phenoxyethanol-antifreeze-neurotoxin.html

Phenol= nephrotoxic; CNS toxin, heart toxin, gastrointestinal, kidney, lung and blood vessel toxin… known to induce coma’s and death; by far one of the most toxic of all vaccine ingredients.
http://informedcitizensagainstvaccination.blogspot.com/2009/11/phenol-cns-toxin-causes-comas-and-death.html

Sorbitol= cardiac toxin, causes neuropathy in and exacerbation of diabetes, CNS toxin, our own government states under no uncertain terms that this substance is NOT to be injected… then allows it to be used in childhood vaccinations.
http://informedcitizensagainstvaccination.blogspot.com/2009/11/sorbitol-cardiac-toxin-causes.html

Neomycin, Streptomycin, Polyxmyxin B, Gentamicin Sulfate= Antibiotics. Immune suppressing, lead to the development of more virulent organisms and antibacterial resistance so people cannot combat them.
http://informedcitizensagainstvaccination.blogspot.com/2009/11/antibiotics-in-vaccinations.html
Egg (chick embryonic fluid), soy, yeast, gelatin= Allergens, risk of anaphylaxis and the development of Asthma.
http://informedcitizensagainstvaccination.blogspot.com/2009/11/allergens-in-vaccinations.html
Monosodium Glutamate= Excitotoxin; hazardous to your health in so many ways: read the full length article for further details.
http://informedcitizensagainstvaccination.blogspot.com/2009/11/monosodium-glutmate-creating-dumb-obese.html

Polysorbate 80 or Tween 80= anaphylaxis risk, also permeates the BBB (blood brain barrier) which means vaccine toxins can enter the brain.
http://informedcitizensagainstvaccination.blogspot.com/2009/11/polysorbate-80-aka-tween-80-allows.html
Chick embryonic fluid, fetal bovine serum, guinea pig embryo cells, monkey kidney cells= Animal products in vaccinations that are highly susceptible to contamination. There is a particularly elevated risk with bovine serum (bovine polyomavirus) and monkey kidney cells (SV40 contamination causing cancer).

What is in the “mediums“? https://vaccineliberationarmy.com/2019/01/15/dogs-cats-increasingly-receiving-psyche-drugs-as-in-humans-its-the-vaccines/

READ MORE FROM ORIGINAL LINK

Animal Products (Contaminants) in Vaccinations

 Animal products in vaccination: Monkey kidney cells, sheep red blood cells, chick embryonic fluid, fetal bovine serum, bovine gelatin, guinea pig embryo cells= risk and history of contamination.
Calf fetus, chick embryo, chick kidney, chicken egg, cow heart, dog kidney, duck egg, guinea pig embryo, horse blood, monkey kidney, monkey lung, mouse blood, pig blood, rabbit brain, sheep blood and others. These are used in various vaccine production lines. Residues are not completely purified out of the final packaged product. Contamination can introduce new pathogens.  READ MORE…
List of ingredients and levels of carcinogenicity,  for each, etc.
See also:

The dangerous impurities of vaccines by Janine Roberts

On the toxic ingredients of vaccinations: plays special emphasis to animal by-products and their production process in vaccinations.

http://www.foresight-preconception.org.uk/pdf/dangerous-impurities-of-vaccines.pdf

Study: Vaccine excipients, xenobiotics-Cause of Inflammation after vaccination?

5G: The extinction event – Sterilizing humanity

VLA Comment: MUST WATCH…1/3 in to it…get to it and complete the video