Vaccine News – I saw an immediate change – VAXXED TV

VAXXED TV – Andy Wakefield

I saw an immediate change
Mother recalls accounts of her son’s changes after vaccination.
Interview recorded on May 6th, 2017 in The United Kingdom

I could not shake the fatigue
Sharon recalls her own accounts of her vaccine responses as well as those of her children.
Interview recorded on May 6th, 2017 in The United Kingdom

Sheila Ealey brings down the house with the biblical story of Gideon! #TxMFA #TxMFA2017

Del Bigtree Speaks at #TxMFA2017 in Houston, Texas
Del Bigtree delivers an inspiring speech concerning the importance of the perception of one’s adversary. What do Tiger Woods, Mike Tyson, Paul Offit, Dorit Reiss, and Richard Pan all have in common?

Stephanie Seneff, PhD Computer Scientist at MIT speaks at #TxMFA #TxMFA2017
Dr. Stephanie Seneff, PhD Computer Scientist of Massachusetts Institute of Technology (MIT), conveys some of the issues surrounding the ubiquitous toxic herbicide, RoundUp (active ingredient, Glyphosate), and its shocking presence in vaccination samples.

Jim Meehan MD

Dr. Ted Fogarty #vaxxed #PrayBig

Joshua Coleman #vaxxed #PrayBig

Nation of Islam #vaxxed #PrayBig

Study – The toxicology of mercury: Current research and emerging trends.

US National Library of Medicine
National Institutes of Health – Nov 2017

Bjørklund G – 1, Dadar M – 2, Mutter J – 3, Aaseth J – 4.
Author information
1 Council for Nutritional and Environmental Medicine, Toften 24, 8610 Mo i Rana, Norway. Electronic address: bjorklund@conem.org.
2 Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran.
3 Paracelsus Clinica al Ronc, Castaneda, Switzerland.
4 Innlandet Hospital Trust and Inland Norway University of Applied Sciences, Elverum, Norway.

Abstract
Mercury (Hg) is a persistent bio-accumulative toxic metal with unique physicochemical properties of public health concern since their natural and anthropogenic diffusions still induce high risk to human and environmental health. The goal of this review was to analyze scientific literature evaluating the role of global concerns over Hg exposure due to human exposure to ingestion of contaminated seafood (methyl-Hg) as well as elemental Hg levels of dental amalgam fillings (metallic Hg), vaccines (ethyl-Hg) and contaminated water and air (Hg chloride). Mercury has been recognized as a neurotoxicant as well as immunotoxic and designated by the World Health Organization as one of the ten most dangerous chemicals to public health. It has been shown that the half-life of inorganic Hg in human brains is several years to several decades. Mercury occurs in the environment under different chemical forms as elemental Hg (metallic), inorganic and organic Hg. Despite the raising understanding of the Hg toxicokinetics, there is still fully justified to further explore the emerging theories about its bioavailability and adverse effects in humans. In this review, we describe current research and emerging trends in Hg toxicity with the purpose of providing up-to-date information for a better understanding of the kinetics of this metal, presenting comprehensive knowledge on published data analyzing its metabolism, interaction with other metals, distribution, internal doses and targets, and reservoir organs.

Study – Systematic Review and Meta-analysis: When One Study Is Just not Enough

Clinical Journal of the American Society of Nephrology

Amit X. Garg*, Dan Hackam † , Marcello Tonelli ‡
– Author Affiliations
*Division of Nephrology and Department of Epidemiology and Biostatistics, University of Western Ontario, London, and †Division of Clinical Pharmacology and Toxicology, University of Toronto, and Cardiac Rehabilitation and Secondary Prevention Program, Toronto Rehabilitation Institute, Toronto, Ontario, and ‡Division of Nephrology and Department of Public Health Sciences, University of Alberta, and Institute of Health Economics, Edmonton, Alberta, Canada

Conclusions
Like all types of research, systematic reviews and meta-analyses have both potential strengths and weaknesses. With the growth of renal clinical studies, an increasing number of these types of summary publications will certainly become available to nephrologists, researchers, administrators, and policy makers who seek to keep abreast of recent developments. To maximize their advantages, it is essential that future reviews be conducted and reported properly, with judicious interpretation by the discriminating reader.

Study – The association between mercury levels and autism spectrum disorders: A systematic review and meta-analysis

Journal of Trace Elements in Medicine and Biology
Volume 44, December 2017, Pages 289-297

Abstract

Background & aims
The relationship between mercury and autism spectrum disorders (ASD) has always been a topic of controversy among researchers. This study aimed to assess the relationship between ASD and mercury levels in hair, urine, blood, red blood cells (RBC), and brain through a meta-analysis.

Methods
A systematic search was performed in several databases including PubMed, ISI Web of Science, Cochrane register of controlled trials, Google Scholar, Scopus, and MagIran until June 2017. Case-control studies evaluating concentration of total mercury in different tissues of ASD patients and comparing them to the healthy subjects (control group) were identified. Necessary data were extracted and random effects model was used to calculate overall effect and its 95% corresponding confidence interval (CI) from the effect sizes.

Results
A total of 44 studies were identified that met the necessary criteria for meta-analysis. The mercury level in whole blood (Hedges = 0.43, 95% CI: 0.12, 0.74, P = 0.007), RBC (Hedges = 1.61, 95% CI: 0.83, 2.38, P < 0.001), and brain (0.61 ng/g, 95% CI, 0.02, 1.19, P = 0.043) was significantly higher in ASD patients than healthy subjects, whereas mercury level in hair (−0.14 mg/g, 95% CI: −0.28, −0.01, P = 0.039) was significantly lower in ASD patients than healthy subjects. The mercury level in urine was not significantly different between ASD patients and healthy subjects (0.51 mg/g creatinine, 95% CI: −0.14, 1.16, P = 0.121).

Conclusions
Results of the current meta-analysis revealed that mercury is an important causal factor in the etiology of ASD. It seems that the detoxification and excretory mechanisms are impaired in ASD patients which lead to accumulation of mercury in the body. Future additional studies on mercury levels in different tissues of ASD patients should be undertaken.

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How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:

Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.

Highly toxic squalene MF59 adjuvant that caused Gulf War syndrome in military

Big Drop In Reported Flu Cases
Less than half of the residents in Windsor-Essex have received their flu shot this season, but the local health unit is reporting a drop in the number of influenza cases.

The opening sentence really tells us a lot (not all, but a lot) of what we need to know. Lots of residents aren’t getting a flu shot, lots or residents aren’t getting the flu. Valid? Not totally, but that’s a decent start. We now find out that there is a 94% decrease in confirmed flu cases from the prior year. What do we also know? I remind you, less than half of residents got a flu shot. So what conclusion is drawn by health officials? That flu shots are helping stave off the flu.
The sentence which follows this ridiculous conclusion is none other than verifiable stats backing up the low number of flu shots, citing 40%. Let’s abort the premise that this article is a ridiculous fallacy and move on to more grand concepts. First, if flu cases are down to minuscule occurrences, wouldn’t it be best to simply stay the path? Why try to fix something which isn’t broken? Clearly, that’s rhetorical on my part because I know the answer to be for pharmaceutical companies to create revenue. That answer hides in plain site. How could you even deny it? There are hardly any flu cases. People aren’t getting flu shots. So your suggestion is to give people more flu shots. What else besides egregious profiteering exist here?
The above article is a perfect example of agenda-ridden garbage. I can’t say that the media outlet itself intentionally conspires in nefarious ways, I think it actually might be utter stupidity on behalf of an editorial staff which is exposed by national health agencies. The article is embarrassing but consistent with worldwide journalistic ineptness. But the worst part is that people will read this and interpret logic. And this is far from logic.

FLUAD™ Flu Vaccine With Adjuvant

What is FLUAD™?
FLUAD™ is a standard-dose, three-component (trivalent) inactivated flu vaccine that contains an adjuvant. It is manufactured using an egg-based process (like most flu vaccines), and is formulated with the adjuvant MF59. An adjuvant is an ingredient added to a vaccine that helps create a stronger immune response to vaccination.
What is MF59?
MF59 is an oil-in-water emulsion of squalene oil. Squalene, a naturally occurring substance found in humans, animals and plants, is highly purified for the vaccine manufacturing process. FLUAD™ is approved for use among people 65 years and older, who often have a lower protective immune response after flu vaccination compared to younger, healthier people.

Highly toxic squalene MF59 adjuvant that caused Gulf War syndrome in military servicemen now being added to some civilian flu vaccines
At a 2010 gathering of the American Rally for Personal Rights in Chicago, registered nurse and retired Air Force Captain Richard Rovet warned his listening audience about the dangers of squalene MF59, the devastation and horrors of which he witnessed first hand during his time in the service. The experimental oil-in-water adjuvant, which was forced on all servicemen beginning in 1999 via the mandatory anthrax vaccine, caused many of Capt. Rovet’s comrades to suffer severe and permanent side effects. One of Capt. Rovet’s closest friends, in fact, was actually killed as a result of squalene MF59.
“For the past 64 years, the United States Military and other agencies within our government have used our servicemen and women as test subjects, oftentimes in secret and without informed consent,” explained Capt. Rovet. “In December of 1994, the United States Senate released a report titled, ‘Is military research hazardous to a veteran’s health? Lessons spanning half a century’ … [that] outlines the unethical use of servicemen and women as test subjects, guinea pigs.”
After establishing that squalene MF59 was admittedly experimental, Capt. Rovet went on to explain how the U.S. government willfully ignored all documented evidence showing that the anthrax vaccine, and squalene MF59 in particular, was directly responsible for triggering an epidemic of Gulf War syndrome that left hundreds of thousands of servicemen seriously injured or dead. Not only this, but the U.S. Department of Defense actually ordered that both the anthrax vaccine and a related botulism toxoid vaccine, both of which contained experimental squalene MF59, not be annotated in soldiers’ medical records — they were instead generically identified as “Vac A” and “Vac B” in order to conceal their identity.
“Roughly one in four of the 697,000 veterans, my brothers and sisters who served in the first Gulf War, are afflicted with Gulf War illness … [and] study after study shows a higher rate of Gulf War illness in vaccinated veterans. That’s a fact,” added Capt. Rovet. “Military members can be ordered to take medicines and vaccines against their will, or be imprisoned and discharged from the armed forces with a criminal record for the rest of their lives, right up there with rape perpetrators.”

Gulf war syndrome linked to a toxic vaccine ingredient
Squalene was used as an adjuvant in compulsory anthrax vaccinations given to servicemen during the Gulf War. Adjuvants are substances added to vaccines to create a stronger immune response to the vaccine. The anthrax vaccines used an oil-in-water emulsion of squalene known as MF59.
Many health activists maintain that the U.S. government willfully ignored evidence showing that MF59 in anthrax vaccine triggered Gulf war syndrome.  Initially the Department of Defense denied squalene’s presence in the compulsory vaccines, but the FDA found evidence of the substance, and tests detecting anti-squalene antibodies in Gulf War Syndrome patients provided a clear link.
How does squalene harm the human body?
Squalene is a naturally occurring substance in animals, plants and humans. Found in abundant supply throughout the nervous system and brain, squalene is actually a beneficial antioxidant when consumed.
But, injecting squalene as an adjuvant is a different story.  Adjuvants enhance the immune response and cause the immune system to overreact to the introduction of the organism being vaccinated against. Experts report that the immune system is triggered to attack squalene throughout the entire body – even where it is vital to the nervous system.  In truth, studies confirm that adjuvants like squalene can generate long-term, concentrated and unremitting immune responses.
In a study published in the American Journal of Pathology in 2000, a single injection of squalene caused rheumatoid arthritis – an autoimmune disease – in rats. Is it surprising in any way that an overwhelming amount of Gulf war syndrome patients suffer from autoimmune diseases?
Incidentally, adjuvants are used to make it possible to use smaller amounts of a flu vaccine, thus allowing for a greater amount of individual doses – and greater profits for the pharmaceutical companies.

Three health care workers in Spokane diagnosed with Guillain-Barré syndrome

Liz Phenneger, a nurse who used to work at Deaconess Hospital, is currently recovering from Guillain-Barré at St. Luke’s Rehabilitation Institute.
She started feeling weak following a flu vaccine and was diagnosed on Oct. 24.
Phenneger spent almost two weeks at Sacred Heart before moving to St. Luke’s for recovery and said she still has limited strength. At times, she feels like she’s “holding on to an electrical wire.”
“I can’t bend my feet, it just feels like I’m wearing big boots or something,” she said.

Lotion ingredient paraben may be more potent carcinogen than thought

Lotion ingredient paraben may be more potent carcinogen than thought
A controversial group of chemicals commonly found in lotions and other personal care products may be more dangerous at low doses than previously thought, according to a new study.
Parabens, which are common ingredients in personal care products, may interact with growth factors in the body to increase the risk of breast cancer. iStock photo
The chemicals, called parabens, are preservatives widely used in everything from shampoos and cosmetics to body lotions and sunscreens. The chemicals have generated increasing health concerns, however, because they mimic estrogens, which have been linked to an increased risk of breast cancer and reproductive problems.
“Although parabens are known to mimic the growth effects of estrogens on breast cancer cells, some consider their effect too weak to cause harm,” said lead investigator Dale Leitman, a gynecologist and molecular biologist at UC Berkeley and an adjunct associate professor of nutritional sciences and toxicology. “But this might not be true when parabens are combined with other agents that regulate cell growth.”
Existing chemical safety tests, which measure the effects of chemicals on human cells, look only at parabens in isolation, he said. They fail to take into account that parabens could interact with other types of signaling molecules in the cells to increase breast cancer risk.

Acetaminophen (Tylenol) Harmful for Babies

Acetaminophen (Tylenol) Harmful for Babies
An article in the New York Times this week warns that prenatal use of acetaminophen—the main ingredient in Tylenol—has been linked to an increased risk of asthma and attention disorders in children whose mothers took the drug.
Acetaminophen is found in over 600 over-the-counter and prescription medications. Petra Arck, professor of fetal-maternal medicine at the University Medical Center Hamburg-Eppendorf, whose rodent experiments have found that acetaminophen stresses the liver and alters the placenta in pregnant mice, told the Times that because it’s so common pregnant women may be taking more acetaminophen than they are aware.
The damage done by acetaminophen seems to be dose dependent—the more a pregnant woman takes, the more serious the effects in her offspring. But since it’s found in so many products, many marketed for babies and children, what if infants, too, are being exposed to damagingly high levels of acetaminophen?
If acetaminophen can harm the fetus during pregnancy, when the baby has the protection of the mother’s liver, as well as the placenta, what if it’s even more harmful when given directly to infants?

But evidence has accumulated that, when taken during pregnancy, acetaminophen may increase the risk that children will develop asthma or attention deficit hyperactivity disorder. The elevated risk in most studies is small, and whether the drug itself is really to blame is debatable. But considering that more than 65 percent of pregnant women in the United States use acetaminophen at some point during their pregnancy, the number of children with problems stemming from it could be substantial.
The odd thing about acetaminophen is that even after decades of widespread use, no one knows precisely how it blunts pain. But it has earned a reputation for strange side effects. Experiments indicate that it impedes people’s ability to empathize. It may undercut the brain’s ability to detect errors. When taken after a vaccine, it may suppress the immune system. Why might the drug affect both asthma and A.D.H.D. rates? Scientists have variously speculated that it could tweak the immune system during pregnancy, or disrupt hormones, or change growth factors in the developing brain. In short, no one knows.

Acetaminophen is the most common drug ingredient in America. There are more than 600 medicines that contain acetaminophen, including over-the-counter (OTC) and prescription (Rx) medicines. Below is a list of some common brand-name medicines, some forms of which contain acetaminophen.

Some Common Over-the-Counter Brand Name Drugs That Contain Acetaminophen

Actifed®
Alka-Seltzer Plus®
Anacin®
Cepacol®
Contac®
Coricidin®
Dayquil®
Dimetapp®
Dristan®
Excedrin®
Feverall®
Formula 44®
Goody’s® Powders
Liquiprin®
Midol®
Mucinex®
Nyquil®
Panadol®
Robitussin®
Saint Joseph® Aspirin-Free
Singlet®
Sinutab®
Sudafed®
Theraflu®
Triaminic®
TYLENOL® Brand Products
Vanquish®
Vicks®
*And store brands

Some Common Prescription Drugs That Contain Acetaminophen (or APAP)

Butalbital®
Endocet®
Fioricet®
Hycotab®
Hydrocet®
Hydrocodone Bitartrate®
Lortab®
MIDRIN®
NORCO®
Oxycodone®
Percocet®
Phenaphen®
ROXICET ™
Sedapap®
Tapanol®
Tramadol
TYLENOL® with Codeine
Tylox®
Ultracet®
Vicodin®
Zydone®
*And generic drugs