The Alex Jones Channel – Shocking! Elmo Lies To Children About Vaccine Safety / Laughs At Autistic Victim
The First 6 Years Of A Fully Vaccinated Child’s Life Looks Like This…
We want you to have a choice. We want you to always know the facts. No laws should govern your child’s medical decisions, only you should.
Here is a comprehensive list of what your child receives if you fully vaccinate them for the first six years of their life.
Source: “What The Pharmaceutical Companies Don’t Want You To Know About Vaccines” – By Dr. Todd M. Elsner. Todd’s book is available on Amazon here.
Dr. Tenpenny’s Book is currently available on Amazon
17,500 mcg 2-phenoxyethanol (antifreeze)
5,700 mcg aluminum (neurotoxin)
Unknown amounts of fetal bovin serum(aborted cow blood)
801.6 mcg formaldehyde (carcinogen, embalming agent)
23,250 mcg gelatin (ground up animal carcuses)
500 mcg human albumin (human blood)
760 mcg of monosodium L-glutamate (causes obesity & diabetis)
Unknown amounts of MRC-5 cells (aborted human babies)
Over 10 mcg neomycin (antibiotic)
Over 0.075 mcg polymyxin B (antibiotic)
Over 560 mcg polysorbate 80 (carcinogen)
116 mcg potassium chloride (used in lethal injection)
188 mcg potassium phosphate (liquid fertilizer agent)
260 mcg sodium bicarbonate (baking soda)
70 mcg sodium borate (Borax, used for cockroach control)
54,100 mcg of sodium chloride (table salt)
Unknown amounts of sodium citrate (food additive)
Unknown amounts of sodium hydroxide (Danger! Corrosive)
2,800 mcg sodium phosphate (toxic to any organism)
Unknown amounts of sodium phosphate monobasic monohydrate (toxic to any organism)
32,000 mcg sorbitol (Not to be injected)
0.6 mcg streptomycin (antibiotic)
Over 40,000 mcg sucrose (cane sugar)
35,000 mcg yeast protein (fungus)
5,000 mcg urea (metabolic waste from human urine)
Other chemical residuals
What The Pharmaceutical Companies Don’t Want You To Know About VACCINES… Paperback – 2009
This book is a must read for parents, soon to be parents and physicians who regularly administer vaccines. There are over 500 pages of information proving that vaccines are not responsible for the eradication of communicable disease; vaccines have done nothing but promote chronic disease and illness; and vaccines contain the most toxic chemicals known to man. Furthermore, there are close to 2,000 references that back up the information in this book. The references are from studies published in peer reviewed medical journals, the Centers for Disease Control and Prevention, the Food and Drug Administration, the prestigious Institute of Medicine, and from the United States Congressional Reform Committee. Lastly, this book contains all the U.S. licensed vaccines and the ingredients each vaccine contains. The ingredients of each vaccine come directly from the pharmaceutical companies’ vaccine package insert which are cross referenced with the National Library of Medicine for their human health effects-You will be SHOCKED at the side effects these vaccine ingredients have on the human body! FACT: If anyone from the medical community wants to argue with the information in this book, they will argue among themselves-it is their information!
Ever wonder WHY we NEED a religious exemption from vaccines?
Are you aware that some vaccines are made from ABORTIONS?
Marcella Piper-Terry explains in detail how abortions are used in vaccine manufacturing and the implications of that.
Interview by Polly Tommey and camera by Joshua Coleman and Anu Vaidya with editing by Joshua Coleman.
Countless teenage girls suffer paralysis, blood clots, brain damage and chronic pain from force-vaccination of Gardasil’s HPV “shot in the dark”
Friday, March 17, 2017 by: S.D. Wells
(Natural News) A sexually transmitted disease called human papillomavirus (HPV) is the only form of cancer known to be contagious, but what the medical community won’t tell parents of teenagers and preteens is that HPV is easily defeated by a normal functioning immune system. Of the 120 or more different strains of HPV, only about 15 are carcinogenic, and the HPV vaccines, which have never been proven safe or effective in any clinical trials, literally take a shot in the dark at a couple of these strains, much like the haphazard flu shot administered every year to tens of millions of unsuspecting victims of neurological poisoning.
Still, the CDC and rogue hacks and shills from Big Pharma use scare tactics to all but force-vaccinate girls as young as 9-years-old with sodium chloride and two versions of the dormant HPV cancers hidden in protein and genetically modified organisms.
Scare tactics and medical propaganda con mothers into getting their young daughters jabbed with deadly neurotoxins
“You won’t be able to have children if you get cervical cancer.” “You can catch cancer from having sex and die.” “The shot will make you immune to cancer.” “The shot prevents cancer.” “You wanna have children later? You better get this shot.” The propaganda is mind-blowing, and it unfortunately works. It convinces parents to do the unthinkable: have their little girls (and boys) jabbed with some of the most dangerous carcinogens on earth to “prevent” a couple of strains of a rather benign, pre-cancerous STD. It doesn’t even make sense. What’s even worse is that the HPV vaccine’s protection effect wears off after a few years (as does the cancer itself under normal immune conditions), so what’s the use of taking the risk of getting jabbed with all these neurotoxins? Just how young are kids becoming promiscuous enough to worry about STDs anyhow?
More than 10,000 adverse events have been reported from victims of the HPV scam, including blood clots in the heart and lungs, anaphylactic shock, loss of muscle use and seizures. Most infections from HPV are benign and cleared rapidly by the human immune system and never progress to cervical cancer, or even precancerous lesions of the vagina, vulva or anus. No valid reason for administering the HPV vaccine has ever even been established.
Why are HPV vaccines, like Gardasil (made by Merck) and Cervarix (made by GSK) so dangerous? Answer: They’re made with “denatured” forms and fragmented strains of the virus, meaning the virus is weakened and can remain dormant for months, if not years, so if you do get the virus later, who’s to say you didn’t get it from the vaccine itself? No studies on this have ever been conducted, nor will they likely ever be. Plus, Gardasil contains aluminum, sodium chloride, polysorbate 80 and l-histidine, the latter of which interferes with the brain’s defenses against metal toxins. That means the aluminum has a heightened chance of crossing the blood/brain barrier. Got brain damage? No wonder. The following are just four examples of the hundreds (if not thousands) of girls permanently damaged by HPV vaccines.
Stronger More Toxic Gardasil Vaccine Approved by FDA: Will More Girls Suffer and Die?
March 23, 2017
Malfeasance is when a public official violates the public trust by performing an act that is wrongful, legally unjustified, or contrary to law. Nonfeasance is the failure to act where there is a duty to act. Misfeasance is conduct that is lawful but inappropriate. Perhaps, when it comes to the recent approval of Gardasil 9 all of these apply.
10 December 2014: The FDA approved the use of a reportedly “new and improved” version of Gardasil, which will be marketed as Gardasil 9. According to the FDA approval letter, this action was taken without consultation with VRBPAC (the Vaccines and Related Biological Products Advisory Committee) which is responsible for reviewing and evaluating data concerning the safety, effectiveness, and appropriate use of vaccines and related biological products.
The FDA approval letter, signed by Marion Gruber, Director of Office of Vaccines Research and Review CBER, states the reason for bypassing the advice of VRBPAC writing:
”We did not refer your application to the Vaccines and Related Biological Products Advisory Committee because our review of information submitted in your BLA, including the clinical study design and trial results, did not raise concerns or controversial issues which would have benefited from an advisory committee discussion.”
So, the Office of Vaccines Research and Review, Center for Biologics Evaluation and Research (CBER) committee took it upon themselves to decide there were ”no concerns or controversial issues” regarding the approval of Gardasil 9?
This division of CBER decided there would be no benefit from ”an advisory committee discussion”?
According to their own mission statement, the FDA is ”responsible for protecting the public health by assuring the safety, efficacy and security of human and veterinary drugs, biological products, medical devices, our nation’s food supply, cosmetics, and products that emit radiation.”
The FDA, and all committees associated with the FDA, are public officials and therefore obliged to act in the public’s best interest particularly when it comes to health and safety issues.
Is bypassing advisory committee discussions regarding Gardasil 9’s potential safety and efficacy acting in the public’s best interest, or is it malfeasance, nonfeasance and/or misfeasance?
Gardasil 9 Facts: More than DOUBLE the amount of Toxic Aluminum!
CBER decided there was no need for VRBPAC to review or evaluate any data concerning the safety, effectiveness, and appropriate use of Merck’s proposed Gardasil 9 vaccine before making a decision to approve the nine-valent HPV vaccine. This move is particularly disturbing when one considers the worldwide controversy surrounding Gardasil’s safety, effectiveness and appropriate use.
Studies about the aluminium toxicity on humans
Gardasil 9 insert
Dr. Yehuda Shoenfeld says vaccines cause auto-immunity. It’s really not a question of “IF” there are adverse events from vaccines, it’s a question of “how often?”, “how severe?”, and whether it’s worth the trade-off? You can listen to the pre-eminent expert on vaccine-induced autoimmunity in the world, or you can go to your mainstream pediatrician who will tell you that vaccines have “no risk, lots of benefits.” It’s really up to you!
This is just a clip from his talk, entire talk in comments below, as well as Dr. Shoenfeld’s new TEXTBOOK, called “Vaccines and Autoimmunity”!
By the way, “autoimmunity” includes all the crazy epidemics in our kids that weren’t around in the 1980s or earlier: asthma, food allergies, skin rashes, etc. “Some of the main examples of autoimmune disorders include diabetes mellitus type 1 (IDDM), systemic lupus erythematosus (SLE), Hashimoto’s thyroiditis, Graves’ disease of the thyroid, Sjögren’s syndrome, Churg-Strauss Syndrome, Coeliac disease, rheumatoid arthritis (RA), and idiopathic thrombocytopenic purport.”
Listen to Dr. Shoenfeld: “Dr. Yehuda Shoenfeld is on the editorial board of 43 journals in the fields of rheumatology and autoimmunity and is the founder and editor of the Israel Medical Association Journal, the representative journal of science and medicine in the English language in Israel. He is also is the founder and editor of “Autoimmunity Reviews” and co-editor of “The Journal of Autoimmunity”. His clinical and scientific works focus on autoimmune and rheumatic diseases, and he has published more than 1700 papers in journals such as the New England Journal of Medicine, Nature, the Lancet, the Proceedings of the National Academy of Sciences of the United States of America, the Journal of Clinical Investigation, the Journal of Immunology, Blood, the Journal of the Federation of American Societies for Experimental Biology, the Journal of Experimental Medicine, Circulation, Cancer, and others, and his articles have had over 31,000 citations. He has written more than three hundred and fifty chapters in books, and has authored and edited 25 books.”
A study from West Africa’s Guinea-Bissau discovered that all-cause infant mortality more than doubled after the introduction of the DTP vaccination.
An observational study from the West African country Guinea-Bissau titled, “The Introduction of Diphtheria-Tetanus-Pertussis and Oral Polio Vaccine Among Young Infants in an Urban African Community: A Natural Experiment,” [i] examined the introduction of diphtheria-tetanus-pertussis (DTP) and oral polio vaccine (OPV) in an urban community in Guinea-Bissau in the early 1980s. The World Health Organization introduced the Expanded Program on Immunization (EPI) in low-income countries in the 1970s with the goal of universal immunization for all children. In the introduction, the study’s authors state, “Except for the measles vaccines, surprisingly few studies examined the introduction of vaccines and their impact on child survival.”
The purpose of the study was to examine what happens to child survival when DTP and OPV were introduced in low-income countries. A community study [ii] of the state of nutrition and family structure found that severe malnutrition was not evident in urban Guinea-Bissau although it was initially assumed to be the main cause of the under-five mortality rate.
The study findings emerged from a child population that had been followed with 3-monthly nutritional weighing sessions since 1978. From June 1981 DTP and OPV were offered from 3 months of age at these sessions. Due to the 3-monthly intervals between sessions, the children were allocated by birthday in a ‘natural experiment’ to receive vaccinations early or late between 3 and 5 months of age. The study included children who were greater than 6 months of age when vaccinations started and children born until the end of December 1983. The researchers compared mortality between 3 and 5 months of age of DTP-vaccinated and not-yet-DTP- vaccinated children in Cox proportional hazard models.
When mortality was compared, the mortality hazard ratio (HR) among 3-5-month-old children having received the DTP (±OPV) was 5.00 compared with not-yet-DTP-vaccinated children [i.e. a 400% increase]. According to the authors, differences in background factors did not explain the effect. All-cause infant mortality after 3 months of age increased after the introduction of these vaccines (2.12 (1.07–4.19)) [i.e. a 212% increase]. However, the study findings revealed the negative effect was particularly strong for children who had received DTP-only and no OPV (10.0 (2.61–38.6)).
The researchers concluded:
“DTP was associated with increased mortality; OPV may modify the effect of DTP.”
Study – The Introduction of Diphtheria-Tetanus-Pertussis and Oral Polio Vaccine Among Young Infants in an Urban African Community: A Natural Experiment
We examined the introduction of diphtheria-tetanus-pertussis (DTP) and oral polio vaccine (OPV) in an urban community in Guinea-Bissau in the early 1980s.
The child population had been followed with 3-monthly nutritional weighing sessions since 1978. From June 1981 DTP and OPV were offered from 3 months of age at these sessions. Due to the 3-monthly intervals between sessions, the children were allocated by birthday in a ‘natural experiment’ to receive vaccinations early or late between 3 and 5 months of age. We included children who were <6 months of age when vaccinations started and children born until the end of December 1983. We compared mortality between 3 and 5 months of age of DTP-vaccinated and not-yet-DTP-vaccinated children in Cox proportional hazard models.
Among 3–5-month-old children, having received DTP (±OPV) was associated with a mortality hazard ratio (HR) of 5.00 (95% CI 1.53–16.3) compared with not-yet-DTP-vaccinated children. Differences in background factors did not explain the effect. The negative effect was particularly strong for children who had received DTP-only and no OPV (HR = 10.0 (2.61–38.6)). All-cause infant mortality after 3 months of age increased after the introduction of these vaccines (HR = 2.12 (1.07–4.19)).
DTP was associated with increased mortality; OPV may modify the effect of DTP.