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Old 19-01-2018, 09:39 AM   #321
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Glyphosate and Fungicides Attract Honey Bees To Them – Bee Decline
Posted on January 18, 2018

By Natural Blaze
Turns out that Monsanto’s Big Ag weedkiller and fungicides might lure bees like….well, like a flower to a bee. And like a sweet poison…

Recently, we reported the a surprising culprit behind the bee decline might actually be fungicides. It does appear that fungicides were an overlooked poison to the bees and there might now be a connection. Just on the heels of this discover, we find more disturbing news…

The journal Scientific Reports states this alarming conclusion,

“When given the choice, honey bee foragers prefer to collect sugar syrup laced with the fungicide chlorothalonil over sugar syrup alone.”

Recent studies have linked fungicides to declines in honey bee and wild bee populations. One recent study, for example, found parallels between the use of chlorothalonil and the presence of Nosema bombi, a fungal parasite, in bumble bees. Greater chlorothalonil use also was linked to range contractions in four declining bumble bee species.

Other research has shown that European honey bees have a very limited repertoire of detoxifying enzymes and that exposure to one potentially toxic compound – including fungicides – can interfere with their ability to metabolize others.
https://www.naturalblaze.com/2018/01...oney-bees.html
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Old 19-01-2018, 09:48 AM   #322
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“The Flu” and “Microwave Sickness” Share Many of the Same Symptoms
January 18, 2018
By B.N. Frank

Germs May Be Everywhere But So Are WiFi and Other Sources of Electrical Pollution (Electrosmog).

There’s a whole lot of sickness going on right now. The media is reporting that much of this is due to “The Flu.”

“Microwave Sickness” and “The Flu” actually share many of the same symptoms.

Doctors introduced the term “Microwave Sickness” in the 1950s. It is caused by exposure to WiFi and other sources of Electrical Pollution which is also referred to “Electrosmog.”

What most refer to as “WiFi” is “Wireless Frequency” which is actually Wireless Radiation. WiFi is produced by Microwave Frequency which is actually Microwave Radiation – like what cooks food in a microwave oven. This is also sometimes referred to as RadioFrequency Radiation or RF.

Many medical professionals aren’t aware that as many as 1/3 of the population is “sensitive” to some degree to sources of WiFi and Electrosmog. Symptoms and severity vary.

“Microwave Sickness” is sometimes referred to as “ElectroSensitivity.” Misdiagnosis is common because there are so many symptoms that could be attributed to other health issues or environmental factors. Behavioral, emotional, and mental health are also affected by WiFi and Electrosmog.
https://www.activistpost.com/2018/01...-symptoms.html
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Old 20-01-2018, 08:01 AM   #323
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Microwaves in Europe responsible for millions of cars worth of CO2
By Staff writer 18 Jan 2018, 12:36
Updated: 18 Jan 2018, 12:37

The heat is on for Europe's microwaves as it's revealed they emit as much carbon dioxide as nearly 7m cars. A new study by the University of Manchester worked out the emissions of microwave ovens over their lifetime, from manufacture to disposal, and found that quick, convenient cooking could be costing the environment dear.

"It is electricity consumption by microwaves that has the biggest impact on the environment," the study says. "Efforts to reduce consumption should focus on improving consumer awareness and behaviour to use appliances more efficiently. For example, electricity consumption by microwaves can be reduced by adjusting the time of cooking to the type of food."
https://www.aol.co.uk/cars/2018/01/1.../?ncid=webmail
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Old 20-01-2018, 09:21 AM   #324
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No the way to work, yesterday, i noticed a major uk brand had ran an ad campaign on lots of bus stops.

Aimed at children. With a picture of young girls. One of which was clearly a transgirl....
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Old 20-01-2018, 12:12 PM   #325
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Quote:
Originally Posted by fairyprincess View Post
No the way to work, yesterday, i noticed a major uk brand had ran an ad campaign on lots of bus stops.

Aimed at children. With a picture of young girls. One of which was clearly a transgirl....
Its all part of the 'normalisation' agenda

let me be clear on this...i believe that all humans have human rights so i'm not advocating any sort of prejudice against trans people

What i am saying though is that at the same time that we treat all children with respect we must also explore the possibility that something else is going on here and that there might be an agenda behind it and the problem with 'normalisation' is that it refuses to question what's going on as it directs all resources towards adapting society to a new norm which itself won't stay static as the situation is ever changing
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Old 21-01-2018, 10:07 AM   #326
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Richard E. Lugar: Body of Evidence Suggests New US Biological Warfront Opening
8.01.2018 Author: Henry Kamens
https://journal-neo.org/2018/01/18/r...front-opening/

We know that the Richard E. Lugar Centre in Tbilisi is actually a biological weapons lab. It has always been assumed that the US Department of Defense took over this facility, alongside a string of others in the former Soviet Union, for offensive purpose, and that the “scientific research” into animal and human diseases it claims to be carrying out is merely a front for developing new biological strains, viruses and bacteria, and then testing them on the Georgian population and the agricultural industry, without asking for consent, and even developing new generation vaccines and cures which are often experimental, naturally donated or supported by the US Department of Defence and German medical research facilities.

There is much evidence that these strains are being tested on the population, ironically even pundits got-it-right. More measurable evidence includes the sudden unexplained spikes in various diseases, human and plants, mortality rates. One also needs to mention the great reluctance of medical people in Georgia to talk about such things, other than off the record and in total confidence, not even to be recorded.

Fewer are even willing to discuss the fact that, after millions of dollars have been spent on this “research lab”, because of flawed engineering and substandard safety standards. Ironically it is very difficult, if not impossible, to find a single research paper published in Georgian, and even the clinical studies are done in secret—and without informed consent. Josef Mengele, Nazi doctor, would be impressed with the Georgian project.

This is not all.

The present Georgian government made a great show of taking over this lab as soon as it took office, due to public concern about it, but the US Department of Defense still claims to run it regardless. A number of foreign contract staff at the centre had returned home to die, too many for these to be natural cause, unrelated deaths. If anyone starts asking questions, problems will result, as Ragnar Skre, a Norwegian Journalist found out after attacked at his home by mast men within hours of visiting the lab several years ago.

He thought at the time that robbery was not the purpose and suspected that the attack was connected to him having information on the planned production of biological weapons in Georgia. He had been carrying out journalistic investigation regarding the allegation.

“Even if the production of biological weapon does not start in Georgia, the government does not appreciate to expose the information that there is reserve of biological bacteria in the country,” said Skre in an interview with the Georgian Human Rights Centre.

All these things are matters of public record; even VOA tries to provide a smokescreen for its actual purpose, claiming that it is “politics-and-not-science” is why should Russia is concerned.

But recent developments suggest that the lab has other functions, including the links between DNA groups and bio weapons. It is not simply observing the effects of new biological strains by studying them by manipulating them. There is a strong possibility that one of its purposes is to inflict upon Georgia already proven viruses and bacteria, which no one needs to test.

Many in Russia and Arab countries suspect that they are likely the target of such research. Russian Senator Klintsevich claims that “It is no secret that different ethnic groups react to biological weapons in different ways and that is why the West is meticulously collecting material all across Russia.”
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Old 23-01-2018, 08:43 AM   #327
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What's Transgender Really All About? - Taken From The Worldwide Wake Up Tour

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Old 23-01-2018, 03:26 PM   #328
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children exposed to mercury in vitro are more likely to regress into autism

Vaccines Cause More Autism Than The CDC Will Admit

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Old 23-01-2018, 03:40 PM   #329
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Vaccine fraud exposed: Measles and mumps making a huge comeback because vaccines are designed to fail, say Merck virologists
Monday, November 11, 2013
by Mike Adams, the Health Ranger

Measles and mumps are making a huge comeback in the United States, but doctors and journalists all make the same critical error in understanding why. They blame "parents who don't vaccinate their kids" as the cause, but the real cause -- as revealed by whistleblowing scientists working for top vaccine manufacturers -- is that measles and mumps vaccines are designed to fail from the start.

Measles and mumps are making a huge comeback in the United States, but doctors and journalists all make the same critical error in understanding why. They blame "parents who don't vaccinate their kids" as the cause, but the real cause -- as revealed by whistleblowing scientists working for top vaccine manufacturers -- is that measles and mumps vaccines are designed to fail from the start.

From the False Claims Act complaint:

Merck also added animal antibodies to blood samples to achieve more favorable test results, though it knew that the human immune system would never produce such antibodies, and that the antibodies created a laboratory testing scenario that "did not in any way correspond to, correlate with, or represent real life ... virus neutralization in vaccinated people," according to the complaint.
https://www.naturalnews.com/042864_m...fic_fraud.html
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Old 23-01-2018, 03:52 PM   #330
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The Vaccine Hoax is Over
December 2, 2012 by Starship Earth: The Big Picture

Freedom of Information Act in the UK filed by a doctor there has revealed 30 years of secret official documents showing that government experts have

1. Known the vaccines don’t work
2. Known they cause the diseases they are supposed to prevent
3. Known they are a hazard to children
4. Colluded to lie to the public
5. Worked to prevent safety studies

Those are the same vaccines that are mandated to children in the US.

Educated parents can either get their children out of harm’s way or continue living inside one of the largest most evil lies in history, that vaccines – full of heavy metals, viral diseases, mycoplasma, fecal material, DNA fragments from other species, formaldehyde, polysorbate 80 (a sterilizing agent) – are a miracle of modern medicine.

Freedom of Information Act filed in the US with the CDC by a doctor with an autistic son, seeking information on what the CDC knows about the dangers of vaccines, had by law to be responded to in 20 days. Nearly 7 years later, the doctor went to court and the CDC argued it does not have to turn over documents. A judge ordered the CDC to turn over the documents on September 30th, 2011.

On October 26, 2011, a Denver Post editorial expressed shock that the Obama administration, after promising to be especially transparent, was proposing changes to the Freedom of Information Act that would allow it to go beyond declaring some documents secret and to actually allow government agencies (such as the CDC) to declare some document “non-existent.”

Simultaneous to this on-going massive CDC cover up involving its primary “health” not recommendation but MANDATE for American children, the CDC is in deep trouble over its decades of covering up the damaging effects of fluoride and affecting the lives of all Americans, especially children and the immune compromised. Lawsuits are being prepared. Children are ingesting 3-4 times more fluoride by body weight as adults and “[t]he sheer number of potentially harmed citizens — persons with dental fluorosis, kidney patients tipped into needing dialysis, diabetics, thyroid patients, etc — numbers in the millions.”

The CDC is obviously acting against the health of the American people. But the threat to the lives of the American people posed by the CDC’s behavior does not stop there. It participated in designed pandemic laws that are on the books in every state in the US, which arrange for the government to use military to force unknown, untested vaccines, drugs, chemicals, and “medical” treatments on the entire country if it declares a pandemic emergency.

The CDC’s credibility in declaring such a pandemic emergency is non-existent, again based on Freedom of Information Act. For in 2009, after the CDC had declared the H1N1 “pandemic,” the CDC refused to respond to Freedom of Information Act filed by CBS News and the CDC also attempted to block their investigation. What the CDC was hiding was its part in one of the largest medical scandals in history, putting out wildly exaggerated data on what it claimed were H1N1 cases, and by doing so, created the false impression of a “pandemic” in the US.

The CDC was also covering up e financial scandal to rival the bailout since the vaccines for the false pandemic cost the US billions. And worse, the CDC put pregnant women first in line for an untested vaccine with a sterilizing agent, polysorbate 80, in it. Thanks to the CDC, “the number of vaccine-related “fetal demise” reports increased by 2,440 percent in 2009 compared to previous years, which is even more shocking than the miscarriage statistic [700% increase].

The exposure of the vaccine hoax is running neck and neck with the much older hoax of a deadly 1918-19 flu. It was aspirin that killed people in 1918-19, not a pandemic flu. It was the greatest industrial catastrophe in human history with 20-50 million people dying but it was blamed on a flu. The beginning of the drug industry began with that success (and Monsanto was part of it). The flu myth was used by George Bush to threaten the world with “another pandemic flu that could kill millions” – a terror tactic to get pandemic laws on the books in every state and worldwide. Then the CDC used hoax of the pandemic hoax to create terror over H1N1 and to push deadly vaccines on the public, killing thousands of unborn children and others. (CDC will not release the data and continues to push the same vaccine.)

The hoax of the vaccine schedule is over, exposed by FOIAs in the UK.

The hoax of the CDC’s interest in children’s lives has been exposed by its refusal to respond to a doctor’s FOIAs around its knowledge of vaccine dangers.

The 1918-19 pandemic hoax has been exposed by Dr. Karen Starko’s work on aspirin’s role in killing people.

And despite refusing to respond to FOIAS, the CDC’s scandalous hoax of a 2009 flu pandemic and its part in creating it, was exposed by CBS NEWS.

And the Obama administration, in attempting to salvage the last vestige of secrecy around what is really happening with vaccines, by declaring agency documents non-existent, has made its claim of transparency, non-existent.

But pandemic laws arranging for unknown vaccines to be forced on the entire country are still in place with HHS creating a vaccine mixture that should never be used on anyone and all liability for vaccines having been removed. Meanwhile, a Canadian study has just proven that the flu vaccine containing the H1N1 vaccine which kills babies in utero, actually increases the risk of serious pandemic flu.

Americans who have been duped into submitting their children to the CDC’s deadly vaccines, have a means to respond now. People from every walk of life and every organization, must:

1. take the information from the UK FOIAs exposing 30 years of vaccine lies, the refusal of the CDC to provide any information on what it knows about those lies, and the Obama Administration’s efforts to hide the CDC’s awareness of those lies, and go to their state legislatures, demand the immediate nullification of the CDC vaccine schedule and the pandemic laws.

2. inform every vet. active duty military person, law enforcement people, DHS agents and medical personnel they know, of the vaccine hoax, for their families are deeply threatened, too, but they may not be aware of it or that they have been folded into agency structures by the pharmaceutical industry (indistinguishable from the bankers and oil companies) that would make them agents of death for their country with the declaration of a “pandemic” emergency or “bio-terrorist” attack. It is completely clear now that the terrorism/bioterrorism structures are scams so that any actions taken to “protect” this country using those laws would in fact be what threatens the existence of Americans.

It was aspirin that killed millions in 1918-19. Now it is mandated and unknown, untested vaccines with banned adjuvants in them that threaten the country with millions of deaths. At the same time, the CDC is holding 500,000 mega-coffins, built to be incinerated, on its property outside Atlanta. Not to put to fine a point on this, but it’s clear now that the CDC should not be involved in any way with public health.

Thanks to the Freedom of Information Act (FOIA), we know that vaccines are not a miracle of modern medicine. Any medical or government authority which insists vaccines prevent diseases is either ignorant of government documents (and endless studies) revealing the exact opposite or of the CDC’s attempts to hide the truth about vaccines from the public, or means harm to the public.

Thanks to the Freedom of Information Act (FOIA), we know the vaccine schedule is a hoax.

The health danger to American children and adults are vaccines.
https://2012thebigpicture.wordpress....-hoax-is-over/
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Old 23-01-2018, 03:54 PM   #331
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30 Years of Secret Official Transcripts Show UK Government Experts Cover Up Vaccine Hazards
Posted on March 14, 2012 by ChildHealthSafety

[ED: Readers should note that a paper presented at a scientific conference is a citable reference for publication purposes. That applies to Dr Lucija Tomljenovic’s paper discussed in this article.]

An extraordinary new paper published by a courageous doctor and investigative medical researcher has dug the dirt on 30 years of secret official transcripts of meetings of UK government vaccine committees and the supposedly independent medical “experts” sitting on them with their drug industry connections.

If you want to get an idea of who is responsible for your child’s condition resulting from a vaccine adverse reaction then this is the paper to read. What you have to ask yourself is if the people on these committees are honest and honourable and acting in the best interests of British children, how is it this has been going on for at least 30 years?

This is what everyone has always known but could never prove before now. Pass this information on to others so they can see what goes on in Government health committees behind locked doors.

We quote here from the author’s summary and the paper:

Deliberately concealing information from parents for the sole purpose of getting them to comply with an “official” vaccination schedule could be considered as a form of ethical violation or misconduct. Official documents obtained from the UK Department of Health (DH) and the Joint Committee on Vaccination and Immunisation (JCVI) reveal that the British health authorities have been engaging in such practice for the last 30 years, apparently for the sole purpose of protecting the national vaccination program.

The 45 page paper with detailed evidence can be downloaded here: The vaccination policy and the Code of Practice of the Joint Committee on Vaccination and Immunisation (JCVI): are they at odds? Lucija Tomljenovic, Neural Dynamics Research Group, Dept. of Ophthalmology and Visual Sciences, University of British Columbia, Vancouver, Canada. It was presented at and forms part of the proceedings of The 2011 BSEM Scientific Conference now published online here: The Health Hazards of Disease Prevention BSEM Scientific Conference, March 2011. [ED: BSEM HAVE REORGANISED THEIR WEBSITE AND THIS PAGE NO LONGER EXISTS THERE – Note Added 8 May 2014]

There are other papers also found at that link which you will find an excellent read.

The author, Dr Lucija Tomljenovic writes:

Here I present the documentation which appears to show that the JCVI made continuous efforts to withhold critical data on severe adverse reactions and contraindications to vaccinations to both parents and health practitioners in order to reach overall vaccination rates which they deemed were necessary for “herd immunity”, a concept which with regards to vaccination, and contrary to prevalent beliefs, does not rest on solid scientific evidence as will be explained. As a result of such vaccination policy promoted by the JCVI and the DH, many children have been vaccinated without their parents being disclosed the critical information about demonstrated risks of serious adverse reactions, one that the JCVI appeared to have been fully aware of. It would also appear that, by withholding this information, the JCVI/DH neglected the right of individuals to make an informed consent concerning vaccination. By doing so, the JCVI/DH may have violated not only International Guidelines for Medical Ethics (i.e., Helsinki Declaration and the International Code of Medical Ethics) [2] but also, their own Code of Practice.
https://childhealthsafety.wordpress....ccine-hazards/
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Old 23-01-2018, 03:57 PM   #332
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Vaccine Industry Watchdog Obtains CDC Documents That Show Statistically Significant Risks of Autism Associated with Vaccine Preservative Thimerosal
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Biochemist Brian Hooker, scientific advisor to A Shot of Truth, reveals CDC knew of risks for over a decade.

Charlotte, NC (PRWEB) February 19, 2014

For nearly ten years, Brian Hooker has been requesting documents that are kept under tight wraps by the Centers for Disease Control and Prevention (CDC). His more than 100 Freedom of Information Act (FOIA) requests have resulted in copious evidence that the vaccine preservative Thimerosal, which is still used in the flu shot that is administered to pregnant women and infants, can cause autism and other neurodevelopmental disorders.

Dr. Hooker, a PhD scientist, worked with two members of Congress to craft the letter to the CDC that recently resulted in his obtaining long-awaited data from the CDC, the significance of which is historic. According to Hooker, the data on over 400,000 infants born between 1991 and 1997, which was analyzed by CDC epidemiologist Thomas Verstraeten, MD, “proves unequivocally that in 2000, CDC officials were informed internally of the very high risk of autism, non-organic sleep disorder and speech disorder associated with Thimerosal exposure.”

When the results of the Verstraeten study were first reported outside the CDC in 2005, there was no evidence that anyone but Dr. Verstraeten within the CDC had known of the very high 7.6-fold elevated relative risk of autism from exposure to Thimerosal during infancy. But now, clear evidence exists. A newly-acquired abstract from 1999 titled, “Increased risk of developmental neurologic impairment after high exposure to Thimerosal containing vaccine in first month of life” required the approval of top CDC officials prior to its presentation at the Epidemic Intelligence Service (EIS) conference. Thimerosal, which is 50% mercury by weight, was used in most childhood vaccines and in the RhoGAM® shot for pregnant women prior to the early 2000s.

The CDC maintains there is “no relationship between Thimerosal-containing vaccines and autism rates in children,” even though the data from the CDC’s own Vaccine Safety Datalink (VSD) database shows a very high risk. There are a number of public records to back this up, including this Congressional Record from May 1, 2003. The CDC’s refusal to acknowledge thimerosal’s risks is exemplified by a leaked statement from Dr. Marie McCormick, chair of the CDC/NIH-sponsored Immunization Safety Review at IOM. Regarding vaccination, she said in 2001, “…we are not ever going to come down that it [autism] is a true side effect….” Also of note, the former director of the CDC, which purchases $4 billion worth of vaccines annually, is now president of Merck’s vaccine division.

Dr. Hooker’s fervent hope for the future: “We must ensure that this and other evidence of CDC malfeasance are presented to Congress and the public as quickly as possible. Time is of the essence. Children’s futures are at stake.” A divide within the autism community has led to some activists demanding that compensation to those with vaccine-injury claims be the top priority before Congress. Dr. Hooker maintains that prevention, “protecting our most precious resource – children’s minds,” must come first. “Our elected officials must be informed about government corruption that keeps doctors and patients in the dark about vaccine risks.”

Referring to an organization that has seen its share of controversy this past year, Dr. Hooker remarked, “It is unfortunate that SafeMinds issued a press release on my information, is accepting credit for my work and has not supported a worldwide ban on Thimerosal.”

Brian Hooker, PhD, PE, has 15 years experience in the field of bioengineering and is an associate professor at Simpson University where he specializes in biology and chemistry. His over 50 science and engineering papers have been published in internationally recognized, peer-reviewed journals. Dr. Hooker has a son, aged 16, who developed normally but then regressed into autism after receiving Thimerosal-containing vaccines.
http://www.prweb.com/releases/asot/t...eb11598819.htm
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Old 23-01-2018, 04:13 PM   #333
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Fordham University mumps outbreak affecting only vaccinated students; school bans unvaccinated students anyway
Thursday, February 27, 2014 by: Jonathan Benson, staff writer

One of New York's lesser-known institutions of higher learning is making headlines after 13 confirmed cases, and counting, of mumps emerged on two of its campuses, prompting school officials to impetuously ban all unvaccinated students from attending classes. But these same reports clearly indicate that all affected students had already been vaccinated for mumps, proving once again the utter uselessness of vaccines and the imbecilic tendencies of organizations chained to the vaccine status quo.

According to reports, concerns first arose after several Fordham University students suddenly came down with flu-like symptoms in recent weeks, which later turned out to be adult mumps in every case. The infection numbers continued to swell, prompting an inquiry into the vaccination records of the affected students. But this inquiry revealed that not a single unvaccinated student had contracted the mumps -- only those who had previously been vaccinated for mumps developed the disease.

Nevertheless, Fordham officials have decided to prohibit all unvaccinated students, none of whom have contracted the disease thus far, from attending classes unless or until they agree to provide proof of vaccination. At the same time, all the vaccinated students who contracted mumps are being allowed to continue attending classes after exceeding the supposed contagious stage, a completely irrational policy move that only unfettered adherence to mainstream vaccine dogma.
https://www.naturalnews.com/044087_v...niversity.html
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Old 23-01-2018, 05:12 PM   #334
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Lethal Injection: The Story Of Vaccination

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Old 23-01-2018, 09:33 PM   #335
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Vitamin K given to new borns...

Phytonadione

WARNING - INTRAVENOUS USE

Severe reactions, including fatalities, have occurred during and immediately after the parenteral administration of Phytonadione. Typically these severe reactions have resembled hypersensitivity or anaphylaxis, including shock and cardiac and/or respiratory arrest. Some patients have exhibited these severe reactions on receiving Phytonadione for the first time. The majority of these reported events occurred following intravenous administration, even when precautions have been taken to dilute the Phytonadione and to avoid rapid infusion. Therefore, the INTRAVENOUS route should be restricted to those situations where another route is not feasible and the increased risk involved is considered justified.

Phytonadione Description

Phytonadione is a vitamin, which is a clear, yellow to amber, viscous, odorless or nearly odorless liquid. It is insoluble in water, soluble in chloroform and slightly soluble in ethanol. It has a molecular weight of 450.70.

Phytonadione is 2-methyl-3-phytyl-1, 4-naphthoquinone. Its empirical formula is C31H4602 and its structural formula is:



Phytonadione Injectable Emulsion, USP, is a yellow, sterile, aqueous colloidal solution of vitamin K1, with a pH of 3.5 to 7.0. It is available for injection by the intravenous, intramuscular, and subcutaneous routes.

Each 0.5 mL contains 1 mg Phytonadione (Vitamin K1), 10 mg polysorbate 80, 10.4 mg propylene glycol, 0.17 mg sodium acetate anhydrous, and 0.00002 mL glacial acetic acid. Additional glacial acetic acid or sodium acetate anhydrous may have been added to adjust pH to meet USP limits of 3.5 to 7.0. The air above the liquid in the individual containers has been displaced by flushing with nitrogen during the filling operation.

Phytonadione - Clinical Pharmacology

Phytonadione aqueous colloidal solution of vitamin K1 for parenteral injection, possesses the same type and degree of activity as does naturally-occurring vitamin K, which is necessary for the production via the liver of active prothrombin (factor II), proconvertin (factor VII), plasma thromboplastin component (factor IX), and Stuart factor (factor X). The prothrombin test is sensitive to the levels of three of these four factors—II, Vll, and X. Vitamin K is an essential cofactor for a microsomal enzyme that catalyzes the post-translational carboxylation of multiple, specific, peptide-bound glutamic acid residues in inactive hepatic precursors of factors II, VII, IX, and X. The resulting gamma-carboxyglutamic acid residues convert the precursors into active coagulation factors that are subsequently secreted by liver cells into the blood.

Phytonadione is readily absorbed following intramuscular administration. After absorption, Phytonadione is initially concentrated in the liver, but the concentration declines rapidly. Very little vitamin K accumulates in tissues. Little is known about the metabolic fate of vitamin K. Almost no free unmetabolized vitamin K appears in bile or urine.

In normal animals and humans, Phytonadione is virtually devoid of pharmacodynamic activity. However, in animals and humans deficient in vitamin K, the pharmacological action of vitamin K is related to its normal physiological function, that is, to promote the hepatic biosynthesis of vitamin K dependent clotting factors.

The action of the aqueous colloidal solution, when administered intravenously, is generally detectable within an hour or two and hemorrhage is usually controlled within 3 to 6 hours. A normal prothrombin level may often be obtained in 12 to 14 hours.

In the prophylaxis and treatment of hemorrhagic disease of the newborn, Phytonadione has demonstrated a greater margin of safety than that of the water-soluble vitamin K analogues.
Indications and Usage for Phytonadione

Phytonadione is indicated in the following coagulation disorders which are due to faulty formation of factors II, VII, IX and X when caused by vitamin K deficiency or interference with vitamin K activity.

Phytonadione Injectable Emulsion, USP is indicated in:
— anticoagulant-induced prothrombin deficiency caused by coumarin or indanedione derivatives;
— prophylaxis and therapy of hemorrhagic disease of the newborn;
— hypoprothrombinemia due to antibacterial therapy;
— hypoprothrombinemia secondary to factors limiting absorption or synthesis of vitamin K, e.g., obstructive jaundice, biliary fistula, sprue, ulcerative colitis, celiac disease, intestinal resection, cystic fibrosis of the pancreas, and regional enteritis;
— other drug-induced hypoprothrombinemia where it is definitely shown that the result is due to interference with vitamin K metabolism, e.g., salicylates.
CONTRAINDICATION

Hypersensitivity to any component of this medication.
Warnings

An immediate coagulant effect should not be expected after administration of Phytonadione. It takes a minimum of 1 to 2 hours for measurable improvement in the prothrombin time. Whole blood or component therapy may also be necessary if bleeding is severe.
Phytonadione will not counteract the anticoagulant action of heparin.

When vitamin K1 is used to correct excessive anticoagulant-induced hypoprothrombinemia, anticoagulant therapy still being indicated, the patient is again faced with the clotting hazards existing prior to starting the anticoagulant therapy. Phytonadione is not a clotting agent, but overzealous therapy with vitamin K1 may restore conditionswhich originally permitted thromboembolic phenomena. Dosage should be kept as low as possible, and prothrombin time should be checked regularly as clinical conditions indicate.

Repeated large doses of vitamin K are not warranted in liver disease if the response to initial use of the vitamin is unsatisfactory. Failure to respond to vitamin K may indicate that the condition being treated is inherently unresponsive to vitamin K.
Precautions
Drug Interactions

Temporary resistance to prothrombin-depressing anticoagulants may result, especially when larger doses of Phytonadione are used. If relatively large doses have been employed, it may be necessary when reinstituting anticoagulant therapy to use somewhat larger doses of the prothrombin-depressing anticoagulant, or to use one which acts on a different principle, such as heparin sodium.
Laboratory Tests

Prothrombin time should be checked regularly as clinical conditions indicate.
Carcinogenesis, Mutagenesis, Impairment of Fertility

Studies of carcinogenicity, mutagenesis or impairment of fertility have not been conducted with Phytonadione.
Pregnancy


Pregnancy Category C: Animal reproduction studies have not been conducted with Phytonadione. It is also not known whether Phytonadione can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Phytonadione should be given to a pregnant woman only if clearly needed.
Nursing Mothers

It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Phytonadione is administered to a nursing woman.
Pediatric Use

Hemolysis, jaundice, and hyperbilirubinemia in newborns, particularly in premature infants, may be related to the dose of Phytonadione. Therefore, the recommended dose should not be exceeded (see ADVERSE REACTIONS and DOSAGE AND ADMINISTRATION).
Adverse Reactions

Severe hypersensitivity reactions, including anaphylactoid reactions and deaths have been reported following parenteral administration. The majority of these reported events occurred following intravenous administration (see Box Warning.)

The possibility of allergic sensitivity, including an anaphylactoid reaction, should be kept in mind following parenteral administration.

Transient “flushing sensations” and “peculiar” sensations of taste have been observed, as well as rare instances of dizziness, rapid and weak pulse, profuse sweating, brief hypotension, dyspnea, and cyanosis.

Pain, swelling, and tenderness at the injection site may occur.

Infrequently, usually after repeated injection, erythematous, indurated, pruritic plaques have occurred; rarely, these have progressed to scleroderma-like lesions that have persisted for long periods. In other cases, these lesions have resembled erythema perstans.

Hyperbilirubinemia has been observed in the newborn following administration of Phytonadione. This has occurred rarely and primarily with doses above those recommended. (See PRECAUTIONS, Pediatric Use.)
Overdosage

The intravenous LD50 of Phytonadione Injectable Emulsion, USP in the mouse is 41.5 and 52 mL/kg for the 0.2% and 1.0% concentrations, respectively.
Phytonadione Dosage and Administration

Whenever possible, Phytonadione should be given by the subcutaneous route (see Box WARNING). When intravenous or intramuscular administration is considered unavoidable, the drug should be injected very slowly, not exceeding 1 mg per minute.

Protect from light at all times.

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration,whenever solution and container permit.

Directions for Dilution

Phytonadione may be diluted with 0.9% Sodium Chloride Injection, 5% Dextrose Injection, or 5% Dextrose and Sodium Chloride Injection. Benzyl alcohol as a preservative has been associated with toxicity in newborns. Therefore, all of the above diluents should be preservative-free. (See WARNINGS) Other diluents should not be used. When dilutions are indicated, administration should be started immediately after mixture with the diluent, and unused portions of the dilution should be discarded, as well as unused contents of the vial.

Prophylaxis of Hemorrhagic Disease of the Newborn

The American Academy of Pediatrics recommends that vitamin K1 be given to the newborn. A single intramuscular dose of Phytonadione 0.5 to 1 mg within one hour of birth is recommended.

Treatment of Hemorrhagic Disease of the Newborn

Empiric administration of vitamin K1 should not replace proper laboratory evaluation of the coagulation mechanism. A prompt response (shortening of the prothrombin time in 2 to 4 hours) following administration of vitamin K1 is usually diagnostic of hemorrhagic disease of the newborn, and failure to respond indicates another diagnosis or coagulation disorder.

Phytonadione 1 mg should be given either subcutaneously or intramuscularly. Higher doses may be necessary if the mother has been receiving oral anticoagulants.

Whole blood or component therapy may be indicated if bleeding is excessive. This therapy, however, does not correct the underlying disorder and Phytonadione should be given concurrently.

Anticoagulant-lnduced Prothrombin Deficiency in Adults

To correct excessively prolonged prothrombin time caused by oral anticoagulant therapy 2.5 to 10 mg or up to 25 mg initially is recommended. In rare instances 50 mg may be required. Frequency and amount of subsequent doses should be determined by prothrombin time response or clinical condition (see WARNINGS). If in 6 to 8 hours after parenteral administration the prothrombin time has not been shortened satisfactorily, the dose should
berepeated.
https://www.drugs.com/pro/phytonadione.html
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Old 24-01-2018, 08:26 PM   #336
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US government shipped bio-chem weapons? Absurd!
TOPICS:Jon Rappoport
October 25, 2013

I know. History is boring. People hate it.

“What happened 25 years ago? Forget it. What’s going on with Miley Cyrus? Is she still twerking?”

Nevertheless, I’ll give it a try.

Keep two twerks in mind. In 1975, the US signed on to an international treaty banning the production, use, and stockpiling of biological weapons. Ditto for chemical weapons, in 1993. Another treaty.

Here’s a twerky quote from the Washington Post (9/4/13, “When the US looked the other way on chemical weapons”): “…The administrations of Ronald Reagan and George H.W. Bush authorized the sale to Iraq of numerous items…including poisonous chemicals and deadly biological viruses, such as anthrax and bubonic plague…”

And now, here’s a flurry of boggling twerks…

Twerk One: Between 1985 and 1989, a US 501C3 firm, American Type Culture Collection, sent Iraq up to 70 shipments of various biowar agents, including 21 strains of anthrax.

Twerk Two: Between 1984 and 1989, the CDC (Centers for Disease Control) sent Iraq at least 80 different biowar agents, including botulinum toxoid, dengue virus, and West Nile antigen and antibody.

This information on the American Type Culture Collection and the CDC comes from a report, IRAQ’S BIOLOGICAL WEAPONS PROGRAM, prepared by the Center for Nonproliferation Studies. The report contains ample reference citations.

Twerk Three: Then we have a comprehensive article by William Blum in the April 1998 Progressive called ANTHRAX EXPORT. Blum cites a 1994 Senate report confirming that, in this 1985-1989 time period, US shipments of anthrax and other biowar agents to Iraq were licensed by…drum roll, cymbal crash…the US Dept. of Commerce.

Twerk Four: Blum quotes from the Senate report: “These biological materials were not attenuated or weakened and were capable of reproduction. It was later learned that these microorganisms exported by the United States were identical to those the United Nations inspectors found and removed from the Iraqi biological warfare program.” Boom.

Twerk Five: This 1994 Senate report also indicates that the US exported to Iraq the precursors for chemwar agents, actual PLANS for chemical and biowar production facilities, and chemical-warhead filling equipment. The exports continued until at least November 28, 1989.

Twerk Six: Blum lists a few other biowar agents the US shipped to Iraq. Histoplasma Capsulatum, Brucella Melitensis, Clostridium Perfringens, Clostridium tetani–as well as E. coli, various genetic materials, human and bacterial DNA.

Twerk Seven (the cover-up): Blum also points out that a 1994 Pentagon report dismissed any connection between all these biowar agents and Gulf War Illness. But the researcher who headed up that study, Joshua Lederberg, was actually a director of the US firm that had provided the most biowar material to Iraq in the 1980s: the American Type Culture Collection.

Twerk Eight (one hand washes the other): Newsday revealed that the CEO of the American Type Culture Collection was a member of the US Dept. of Commerce’s Technical Advisory Committee. See, the Dept. of Commerce had to license and approve all those exports of biowar agents carried out by the American Type Culture Collection. Get the picture?

Now, as to other US companies which dealt biowar or chemwar agents to Iraq–all such sales having been okayed by the US government–the names of these companies are contained in records of the 1992 Senate hearings, “United States export policy toward Iraq prior to Iraq’s invasion of Kuwait”:

Twerk Nine (the names of US criminal companies): Mouse Master (Georgia), Sullaire Corp (Charlotte, North Carolina), Pure Aire (Charlotte, North Carolina), Posi Seal (Conn.), Union Carbide (Conn.), Evapco (Maryland), BDM Corp (Virginia), Spectra Physics (Calif.).

There are about a dozen more.

Twerk Ten (dept. of mind-boggling excuses): Hewlett Packard said that the recipient of its shipments, Saad 16, was some sort of school in Iraq. But in 1990, the Wall St. Journal stated that Saad 16 was a “heavily fortified, state-of-the-art [Iraqi] complex for aircraft construction, missile design, and, almost certainly, nuclear-weapons research.”

Twerk Eleven: There has been a considerable debate about whether Saddam hid some of his bio/chem weapons in Syria, to evade UN weapons inspectors. If he did, then is it possible the current situation in Syria has a few of its roots in the US? Is it possible some of Syria’s WMDs originally came from America?

One thing is certain. A US government investigation isn’t going look into that possibility.

Jon Rappoport is the author of two explosive collections, The Matrix Revealed and Exit From the Matrix, Jon was a candidate for a US Congressional seat in the 29th District of California. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free emails at www.nomorefakenews.com
https://www.activistpost.com/2013/10...m-weapons.html
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Old 25-01-2018, 06:49 PM   #337
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Irrefutable, undeniable proof that mercury is still used in vaccines injected into children
Wednesday, January 24, 2018 by: Mike Adams

Because there has been a malicious disinformation effort to convince doctors, nurses and the public that vaccines given to children don’t contain mercury, I’m posting this letter from the State of California Health and Human Services Agency as proof that mercury is still injected into children via vaccines.

As you can see from the letter, authored by Secretary Diana S. Dooley and dated October 9, 2015, when California ran out of mercury-free vaccines, approval was granted to inject children with mercury-laced vaccines containing Thimerosal, a mercury-based preservative chemical. In the words of Diana S. Dooley:

I am granting a temporary exemption from California Health and Safety Code Section 124172 for seasonal influenza vaccine with trace levels of thimerosal to be administered to children younger than three years from October 9, 2015 through December 31, 2015, because the current supply of thimerosal-free vaccine for young children is inadequate…

Read the full letter yourself at this link. (PDF)

Or read the full text of the letter, below.

As further proof that mercury has not been removed from vaccines, note that there is no federal law or FDA ruling that requires the removal of mercury from vaccines. Mercury is still legal to use in vaccines, and in fact as you’ll see in the California letter, it’s still deliberately used in vaccine injections administered to children. This is not in dispute. Anyone who is not aware of these facts is uninformed.

At any moment, any state health authority can simply declare it’s “okay” to use mercury vaccines on children, just as happened in California. There is no federal law preventing it whatsoever. These orders may, in fact, be made entirely without public knowledge or any attempt by state officials to inform the public.
https://www.naturalnews.com/2018-01-...-children.html
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Old 27-01-2018, 08:43 PM   #338
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Microwaves are harmful...

Clinical Study
Metabolic and Genetic Screening of Electromagnetic Hypersensitive Subjects as a Feasible Tool for Diagnostics and Intervention
Chiara De Luca,1,2 Jeffrey Chung Sheun Thai,3 Desanka Raskovic,4 Eleonora Cesareo,4 Daniela Caccamo,5 Arseny Trukhanov,2 and Liudmila Korkina1,2

1Centre of Innovative Biotechnological Investigations (Cibi-Nanolab), Novoslobodskaya Street 36/1, Moscow 127055, Russia
2Active Longevity Clinic “Institut Krasoty na Arbate”, 8 Maly Nikolopeskovsky lane, Moscow 119002, Russia
3Natural Health Farm, 39 Jln Pengacara U1/48, Seksyen U1, Temasya Industrial Park, 40150 Shah Alam, Selangor, Malaysia
42nd Dermatology Division, Dermatology Institute (IDI IRCCS), Via Monti di Creta 104, 00167 Rome, Italy
5Department of Biomedical Sciences and Morpho-Functional Imaging, Polyclinic University of Messina, 98125 Messina, Italy

Received 28 November 2013; Accepted 26 February 2014; Published 9 April 2014

Academic Editor: Beatriz De las Heras

Copyright © 2014 Chiara De Luca et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract

Growing numbers of “electromagnetic hypersensitive” (EHS) people worldwide self-report severely disabling, multiorgan, non-specific symptoms when exposed to low-dose electromagnetic radiations, often associated with symptoms of multiple chemical sensitivity (MCS) and/or other environmental “sensitivity-related illnesses” (SRI). This cluster of chronic inflammatory disorders still lacks validated pathogenetic mechanism, diagnostic biomarkers, and management guidelines. We hypothesized that SRI, not being merely psychogenic, may share organic determinants of impaired detoxification of common physic-chemical stressors. Based on our previous MCS studies, we tested a panel of 12 metabolic blood redox-related parameters and of selected drug-metabolizing-enzyme gene polymorphisms, on 153 EHS, 147 MCS, and 132 control Italians, confirming MCS altered –0.0001) glutathione-(GSH), GSH-peroxidase/S-transferase, and catalase erythrocyte activities. We first described comparable—though milder—metabolic pro-oxidant/proinflammatory alterations in EHS with distinctively increased plasma coenzyme-Q10 oxidation ratio. Severe depletion of erythrocyte membrane polyunsaturated fatty acids with increased ?6/?3 ratio was confirmed in MCS, but not in EHS. We also identified significantly altered distribution-versus-control of the CYP2C19*1/*2 SNP variants in EHS, and a 9.7-fold increased risk (OR: 95% C.–74.5) of developing EHS for the haplotype (null)GSTT1 + (null)GSTM1 variants. Altogether, results on MCS and EHS strengthen our proposal to adopt this blood metabolic/genetic biomarkers’ panel as suitable diagnostic tool for SRI.
https://www.hindawi.com/journals/mi/2014/924184/
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Old 27-01-2018, 08:53 PM   #339
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Diabetes, obesity linked to chemical exposure – Endocrine Society
Published time: 29 Sep, 2015 19:57

Scientific research has increasingly linked common chemicals found in everyday products to diabetes, obesity, cancer, and other major ailments, according to a new policy statement.

Endocrine-disrupting chemicals (EDCs) like bisphenol A and phthalates, found in food can linings, plastics, cosmetics, and pesticides, are common to the point that everyone on Earth has been exposed to one or more. EDCs – which influence the body's natural hormones – mimic, block, or simply interfere with hormone functions, leading to the malformation of cells.

The Endocrine Society now says in a new scientific statement that research in recent years has repeatedly pointed to links between these and other chemicals to not only diabetes and obesity, but infertility and breast cancer.

"In 2015, there is far more conclusive evidence about whether, when, and how endocrine-disrupting chemicals perturb endocrine systems, including in humans," said the Endocrine Society, which includes health specialists involved in EDC research.

"Thus, it is more necessary than ever to minimize further exposures, to identify new endocrine disrupting chemicals as they emerge, and to understand underlying mechanisms in order to develop methods to enable interventions in cases of endocrine disrupting chemical-associated disease. This is especially important because new chemicals may be released into the marketplace without appropriate safety testing."

The publicity was planned to coincide with the International Conference on Chemicals Management in Switzerland, where experts will stress the health risks of EDC exposure and ways to limit harmful EDCs.
https://www.rt.com/usa/316965-endocr...cals-diabetes/
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Old 29-01-2018, 07:02 PM   #340
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Vaccine industry in PANIC MODE as *vaccinated* children keep dying from the flu all across America
Sunday, January 28, 2018 by: Mike Adams

Children are dying from the flu all across America, according to media reports. What the media isn’t reporting, however, is how many of the children who died were also vaccine recipients. Make no mistake: If only unvaccinated children were dying from the flu, that would be the headline everywhere: “Unvaccinated Children Dying Across America” or even “Flu Shot Saves Children from Deadly Influenza.” But of course you’re not seeing those headlines for the simple reason that vaccinated children are among those who are being killed by this year’s flu.

“The dominant Influenza strain this year is H3N2. This particular strain has a history of causing more hospitalizations and more deaths,” reports The Organic Prepper. “In addition to H3N2 producing a more serious infection in general, this year’s particular H3N2 influenza virus is particularly virulent.”

This year’s flu has reportedly killed 44,116 people, according to the CDC. The number of children so far killed by this year’s flu is 37, say CDC statistics. The flu vaccine, widely touted by the clueless media as being some sort of magical “bulletproof vest” against influenza infections, is approaching zero effectiveness.
https://www.naturalnews.com/2018-01-...s-america.html
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