Pure, White and Deadly….

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The man who tried to warn us about sugar in 1972 was suppressed

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By Julia Llewellyn Smith, The Daily Telegraph

A couple of years ago, an out-of-print book published in 1972 by a long-dead British professor suddenly became a collector’s item. Copies that had been lying dusty on bookshelves were selling for hundreds of pounds, while copies were also being pirated online.

Alongside such rarities as Madonna’s Sex, Stephen King’s Rage (written as Richard Bachman) and Promise Me Tomorrow by Nora Roberts; Pure, White and Deadlyby John Yudkin, a book widely derided at the time of publication, was listed as one of the most coveted out-of-print works in the world.

How exactly did a long-forgotten book suddenly become so prized? The cause was a ground-breaking lecture called Sugar: the Bitter Truth by Robert Lustig, professor of paediatric endocrinology at the University of California, in which Lustig hailed Yudkin’s work as “prophetic”.

“Without even knowing it, I was a Yudkin acolyte,” says Lustig, who tracked down the book after a tip from a colleague via an interlibrary loan. “Everything this man said in 1972 was the God’s honest truth and if you want to read a true prophecy you find this book… I’m telling you every single thing this guy said has come to pass. I’m in awe.”

Posted on YouTube in 2009, Lustig’s 90-minute talk has received 4.1 million hits and is credited with kick-starting the anti-sugar movement, a campaign that calls for sugar to be treated as a toxin, like alcohol and tobacco, and for sugar-laden foods to be taxed, labelled with health warnings and banned for anyone under 18.

Lustig is one of a growing number of scientists who don’t just believe sugar makes you fat and rots teeth. They’re convinced it’s the cause of several chronic and very common illnesses, including heart diseasecancerAlzheimer’s and diabetes. It’s alsoaddictive, since it interferes with our appetites and creates an irresistible urge to eat.

This year, Lustig’s message has gone mainstream; many of the New Year diet books focused not on fat or carbohydrates, but on cutting out sugar and the everyday foods (soups, fruit juices, bread) that contain high levels of sucrose. The anti-sugar camp is not celebrating yet, however. They know what happened to Yudkin and what a ruthless and unscrupulous adversary the sugar industry proved to be.

The tale begins in the Sixties. That decade, nutritionists in university laboratories all over America and Western Europe were scrabbling to work out the reasons for an alarming rise in heart disease levels. By 1970, there were 520 deaths per 100,000 per year in England and Wales caused by coronary heart disease and 700 per 100,000 in America. After a while, a consensus emerged: the culprit was the high level of fat in our diets.

One scientist in particular grabbed the headlines: a nutritionist from the University of Minnesota called Ancel Keys. Keys, famous for inventing the K-ration – 12,000 calories packed in a little box for use by troops during the Second World War – declared fat to be public enemy number one and recommended that anyone who was worried about heart disease should switch to a low-fat “Mediterranean” diet.

Instead of treating the findings as a threat, the food industry spied an opportunity. Market research showed there was a great deal of public enthusiasm for “healthy” products and low-fat foods would prove incredibly popular. By the start of the Seventies, supermarket shelves were awash with low-fat yogurts, spreads, and even desserts and biscuits.

But, amid this new craze, one voice stood out in opposition. John Yudkin, founder of the nutrition department at the University of London’s Queen Elizabeth College, had been doing his own experiments and, instead of laying the blame at the door of fat, he claimed there was a much clearer correlation between the rise in heart disease and a rise in the consumption of sugar. Rodents, chickens, rabbits, pigs and students fed sugar and carbohydrates, he said, invariably showed raised blood levels of triglycerides (a technical term for fat), which was then, as now, considered a risk factor for heart disease. Sugar also raised insulin levels, linking it directly to type 2 diabetes.

Factsheet: Type 2 diabetes

When he outlined these results in Pure, White and Deadly, in 1972, he questioned whether there was any causal link at all between fat and heart disease. After all, he said, we had been eating substances like butter for centuries, while sugar, had, up until the 1850s, been something of a rare treat for most people. “If only a small fraction of what we know about the effects of sugar were to be revealed in -relation to any other material used as a food additive,” he wrote, “that material would promptly be banned.”

This was not what the food industry wanted to hear. When devising their low-fat products, manufacturers had needed a fat substitute to stop the food tasting like cardboard, and they had plumped for sugar. The new “healthy” foods were low-fat but had sugar by the spoonful and Yudkin’s findings threatened to disrupt a very profitable business.

As a result, says Lustig, there was a concerted campaign by the food industry and several scientists to discredit Yudkin’s work. The most vocal critic was Ancel Keys.

Keys loathed Yudkin and, even before Pure, White and Deadly appeared, he published an article, describing Yudkin’s evidence as “flimsy indeed”.

“Yudkin always maintained his equanimity, but Keys was a real a––-, who stooped to name-calling and character assassination,” says Lustig, speaking from New York, where he’s just recorded yet another television interview.

The British Sugar Bureau put out a press release dismissing Yudkin’s claims as “emotional assertions” and the World Sugar Research Organisation described his book as “science fiction”. When Yudkin sued, it printed a mealy-mouthed retraction, concluding: “Professor Yudkin recognises that we do not agree with [his] views and accepts that we are entitled to express our disagreement.”

Yudkin was “uninvited” to international conferences. Others he organised were cancelled at the last minute, after pressure from sponsors, including, on one occasion, Coca-Cola. When he did contribute, papers he gave attacking sugar were omitted from publications. The British Nutrition Foundation, one of whose sponsors was Tate & Lyle, never invited anyone from Yudkin’s internationally acclaimed department to sit on its committees. Even Queen Elizabeth College reneged on a promise to allow the professor to use its research facilities when he retired in 1970 (to write Pure, White and Deadly). Only after a letter from Yudkin’s solicitor was he offered a small room in a separate building.

“Can you wonder that one sometimes becomes quite despondent about whether it is worthwhile trying to do scientific research in matters of health?” he wrote. “The results may be of great importance in helping people to avoid disease, but you then find they are being misled by propaganda designed to support commercial interests in a way you thought only existed in bad B films.”

And this “propaganda” didn’t just affect Yudkin. By the end of the Seventies, he had been so discredited that few scientists dared publish anything negative about sugar for fear of being similarly attacked. As a result, the low-fat industry, with its products laden with sugar, boomed.

Yudkin’s detractors had one trump card: his evidence often relied on observations, rather than on explanations, of rising obesity, heart disease and diabetes rates. “He could tell you these things were happening but not why, or at least not in a scientifically acceptable way,” says David Gillespie, author of the bestselling Sweet Poison. “Three or four of the hormones that would explain his theories had not been discovered.”

“Yudkin knew a lot more data was needed to support his theories, but what’s important about his book is its historical significance,” says Lustig. “It helps us understand how a concept can be bastardised by dark forces of industry.”

From the Eighties onwards, several discoveries gave new credence to Yudkin’s theories. Researchers found fructose, one of the two main carbohydrates in refined sugar, is primarily metabolised by the liver; while glucose (found in starchy food like bread and potatoes) is metabolised by all cells. This means consuming excessive fructose puts extra strain on the liver, which then converts fructose to fat. This induces a condition known as insulin resistance, or metabolic syndrome, which doctors now generally acknowledge to be the major risk factor for heart disease, diabetes and obesity, as well as a possible factor for many cancers. Yudkin’s son, Michael, a former professor of biochemistry at Oxford, says his father was never bitter about the way he was treated, but, “he was hurt personally”.

“More than that,” says Michael, “he was such an enthusiast of public health, it saddened him to see damage being done to us all, because of vested interests in the food industry.”

One of the problems with the anti-sugar message – then and now – is how depressing it is. The substance is so much part of our culture, that to be told buying children an ice cream may be tantamount to poisoning them, is most unwelcome. But Yudkin, who grew up in dire poverty in east London and went on to win a scholarship toCambridge, was no killjoy. “He didn’t ban sugar from his house, and certainly didn’t deprive his grandchildren of ice cream or cake,” recalls his granddaughter, Ruth, a psychotherapist. “He was hugely fun-loving and would never have wanted to be deprived of a pleasure, partly, perhaps, because he grew up in poverty and had worked so hard to escape that level of deprivation.”

“My father certainly wasn’t fanatical,” adds Michael. “If he was invited to tea and offered cake, he’d accept it. But at home, it’s easy to say no to sugar in your tea. He believed if you educated the public to avoid sugar, they’d understand that.”

Thanks to Lustig and the rehabilitation of Yudkin’s reputation, Penguin republished Pure, White and Deadly 18 months ago. Obesity rates in the UK are now 10 times what they were when it was first published and the amount of sugar we eat has increased 31.5 per cent since 1990 (thanks to all the “invisible” sugar in everything from processed food and orange juice to coleslaw and yogurt). The number of diabetics in the world has nearly trebled. The numbers dying of heart disease has decreased, thanks to improved drugs, but the number living with the disease is growing steadily.

Related: Why are we fatter than ever?

As a result, the World Health Organisation is set to recommend a cut in the amount of sugar in our diets from 22 teaspoons per day to almost half that. But its director-general, Margaret Chan, has warned that, while it might be on the back foot at last, the sugar industry remains a formidable adversary, determined to safeguard its market position.

Recently, UK food campaigners have complained that they’re being shunned by ministers who are more than willing to take meetings with representatives from the food industry. “It is not just Big Tobacco any more,” Chan said last year. “Public health must also contend with Big Food, Big Soda and Big Alcohol. All of these industries fear regulation and protect themselves by using the same tactics. They include front groups, lobbies, promises of self-regulation, lawsuits and industry-funded research that confuses the evidence and keeps the public in doubt.”

Dr Julian Cooper, head of research at AB Sugar, insists the increase in the incidence of obesity in Britain is a result of, “a range of complex factors”. “Reviews of the body of scientific evidence by expert committees have concluded that consuming sugar as part of a balanced diet does not induce lifestyle diseases such as diabetes and heart disease,” he says.

If you look up Robert Lustig on Wikipedia, nearly two-thirds of the studies cited there to repudiate Lustig’s views were funded by Coca-Cola. But Gillespie believes the message is getting through. “More people are avoiding sugar, and when this happens companies adjust what they’re selling,” he says. It’s just a shame, he adds, that a warning that could have been taken on board 40 years ago went unheeded: “Science took a disastrous detour in ignoring Yudkin. It was to the detriment of the health of millions.”

© Copyright (c) The Daily Telegraph

Amino Sweet…

Posted by: admin  /  Category: Health

 

Aspartame has been Renamed and is Now Being Marketed as a Natural Sweetener…

by Drew Kaplan
Artificial sweeteners especially aspartame has gotten a bad rap over the years, most likely due to studies showing they cause cancer. But not to worry Ajinomoto the company that makes Aspartame has changed the name to AminoSweet. It has the same toxic ingredients but a nice new sounding name.
And if you or your child happens to be allergic to Aspartame, well don’t take it personally it’s just business.

Despite the evidence gained over the years showing that aspartame is a dangerous toxin, it has remained on the global market . In continues to gain approval for use in new types of food despite evidence showing that it causes neurological brain damage, cancerous tumors, and endocrine disruption, among other things.

Most consumers are oblivious to the fact that Aspartame was invented as a drug but upon discovery of its’ sweet taste was magically transformed from a drug to a food additive. HFA wants to warn our readers to beware of a wolf dressed up in sheep’s clothing or in this case Aspartame dressed up as Aminosweet.

Over 25 years ago, aspartame was first introduced into the European food supply. Today, it is an everyday component of most diet beverages, sugar-free desserts, and chewing gums in countries worldwide. But the tides have been turning as the general public is waking up to the truth about artificial sweeteners like aspartame and the harm they cause to health. The latest aspartame marketing scheme is a desperate effort to indoctrinate the public into accepting the chemical sweetener as natural and safe, despite evidence to the contrary.

Aspartame was an accidental discovery by James Schlatter, a chemist who had been trying to produce an anti-ulcer pharmaceutical drug for G.D. Searle & Company back in 1965. Upon mixing aspartic acid and phenylalanine, two naturally-occurring amino acids, he discovered that the new compound had a sweet taste. The company merely changed its FDA approval application from drug to food additive and, voila, aspartame was born.

G.D. Searle & Company first patented aspartame in 1970. An internal memo released in the same year urged company executives to work on getting the FDA into the “habit of saying yes” and of encouraging a “subconscious spirit of participation” in getting the chemical approved.

G.D. Searle & Company submitted its first petition to the FDA in 1973 and fought for years to gain FDA approval, submitting its own safety studies that many believed were inadequate and deceptive. Despite numerous objections, including one from its own scientists, the company was able to convince the FDA to approve aspartame for commercial use in a few products in 1974, igniting a blaze of controversy.

In 1976, then FDA Commissioner Alexander Schmidt wrote a letter to Sen. Ted Kennedy expressing concern over the “questionable integrity of the basic safety data submitted for aspartame safety”. FDA Chief Counsel Richard Merrill believed that a grand jury should investigate G.D. Searle & Company for lying about the safety of aspartame in its reports and for concealing evidence proving the chemical is unsafe for consumption.

The details of aspartame’s history are lengthy, but the point remains that the carcinogen was illegitimately approved as a food additive through heavy-handed prodding by a powerful corporation with its own interests in mind. Practically all drugs and food additives are approved by the FDA not because science shows they are safe but because companies essentially lobby the FDA with monetary payoffs and complete the agency’s multi-million dollar approval process.

Changing aspartame’s name to something that is “appealing and memorable”, in Ajinomoto’s own words, may hoodwink some but hopefully most will reject this clever marketing tactic as nothing more than a desperate attempt to preserve the company’s multi-billion dollar cash cow. Do not be deceived.

Update: As many comments are being posted by readers who are allergic to Aspartame we ask that you please

forward this article to as many people as you can.

Sources:

Ajinomoto brands aspartame ‘AminoSweet’

Aspartame History Highlights

FDA’s approval of aspartame under scrutiny

An Overdue Ban On A Dangerous Sweetener

http://www.naturalnews.com/028151_aspartame_sweeteners.html

 

Infant hospitalizations and deaths…

Posted by: admin  /  Category: Health

A  study, published in Human and Experimental Toxicology, a peer-reviewed journal indexed by the National Library of Medicine, analyzed more than 38,000 reports of infant hospitalizations and deaths following vaccinations.[1] Researchers found statistically significant correlations between the number of vaccine doses administered to infants and infant hospitalization and mortality rates: babies who receive the most vaccines tend to have higher (worse) hospitalization and death rates.

Infants who received 2 vaccines simultaneously were significantly less likely to be hospitalized than infants who received 3 or more vaccines at the same time. Infants who received 3 vaccines simultaneously were significantly less likely to be hospitalized than infants who received 4 or more vaccines at the same time. Babies who received 6, 7, or 8 vaccines during a single pediatric well-baby visit were the most likely to be hospitalized following their injections. In fact, the hospitalization rate increased linearly from 11.0% for infants receiving 2 vaccine doses to 23.5% for infants receiving 8 vaccine doses.

The authors of the study, Dr. Gary Goldman and Neil Z. Miller, also discovered that younger infants were significantly more likely to be hospitalized after receiving vaccinations than older infants. In addition, infants who received 5-8 vaccines simultaneously were significantly more likely to die following their shots than infants who received 1-4 vaccines simultaneously.

Several factors could contribute to whether an infant will have an adverse reaction to vaccines, including a genetic predisposition, illness (which may be a contraindication to vaccine administration), quality of vaccines (which can vary by manufacturing methods), and sensitivity to one or more vaccine components. Some infants might be more likely to experience an adverse reaction due to biochemical or synergistic toxicity associated with concurrent administration of multiple vaccines.

In 1990, infants received a total of 15 vaccine doses prior to their first year of life. By 2007, the Centers for Disease Control and Prevention (CDC) recommended 26 vaccine doses for infants: 3 DTaP, 3 polio, 3 Hib, 3 hepatitis B, 3 pneumococcal, 3 rotavirus, and 2 influenza vaccines.

The CDC’s Childhood Immunization Schedule Was Not Tested for Safety, Lacks Scientific Veracity:

While each childhood vaccine has individually undergone clinical trials to assess safety, studies have not been conducted to determine the safety (or efficacy) of combining vaccines during a single physician visit as recommended by the Centers for Disease Control and Prevention’s (CDC) guidelines. For example, 2-, 4-, and 6-month-old infants are expected to receive vaccines for polio, hepatitis B, diphtheria, tetanus, pertussis, rotavirus, Haemophilus influenzae type B, and pneumococcal, all during a single well-baby visit — even though this combination of 8 vaccines was never tested in clinical trials.

Although the CDC’s recommended childhood immunization schedule a) requires infants to receive up to 8 vaccines simultaneously, b) affects millions of infants annually, and c) was never scientifically tested for safety, the CDC had prior knowledge that combining chemical substances, including prescribed pharmaceuticals, “can produce health consequences that are additive, synergistic, antagonistic, or can

potentiate the response expected from individual component exposures.”[2]

Administering 6, 7, or 8 vaccine doses to an infant during a single physician visit may certainly be more convenient for parents — rather than making additional trips to the doctor’s office — but evidence of a positive association between infant adverse reactions and the number of vaccine doses administered confirms that vaccine safety must remain the highest priority.

The findings in this study show a positive correlation between the number of vaccine doses administered and the percentage of hospitalizations and deaths reported to the Vaccine Adverse Event Reporting System (VAERS). (The VAERS database is an important postmarketing safety surveillance tool that is periodically analyzed by the CDC, FDA, and other vaccine researchers to discover potentially adverse vaccination trends.) In addition, younger infants were significantly more likely than older infants to be hospitalized or die after receiving vaccines. These trends not only have a biological plausibility but are supported by evidence from case reports, case series, and other studies using entirely different methodologies and unique population cohorts. For example, in 2011, Miller and Goldman collaborated on another study showing that among developed nations infant mortality increased with an increase in the number of vaccine doses.[3]

Since vaccines are given to millions of infants annually, it is imperative that health authorities have scientific data from synergistic toxicity studies on all combinations of vaccines that infants might receive. Finding ways to increase vaccine safety should be the highest priority.

You may download the complete study here: Goldman-Miller Vaccine Study (PDF) or here: Goldman-Miller Vaccine Study

Funding Acknowledgment: This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors. The National Vaccine Information Center (NVIC) donated $2500 for open access to the journal article (making it freely available to all researchers). NVIC is dedicated to preventing vaccine injuries and deaths through public education.

References:

1. Relative trends in hospitalizations and mortality among infants by the number of vaccine doses and age, based on the Vaccine Adverse Event Reporting System (VAERS), 1990-2010. Hum Exp Toxicol October 2012; 31(10): 1012-1021.

2. Mixed exposures research agenda: a report by the NORA Mixed Exposures Team. Department of Health and Human Services (DHHS), Centers for Disease Control and Prevention (CDC), National Institute for Occupational Safety and Health (NIOSH); DHHS (NIOSH) 2004. December 2005. p.106: vi.

3. Infant mortality rates regressed against number of vaccine doses routinely given: is there a biochemical or synergistic toxicity? Hum Exp Toxicol September 2011; 30(9): 1420-1428. [Read this study here: Miller-Goldman Vaccine Study (PubMed)]

About the author:
Neil Z. Miller is a medical research journalist and the Director of the Thinktwice Global Vaccine Institute. He has devoted the last 25 years to educating parents and health practitioners about vaccines, encouraging informed consent and non-mandatory laws. He is the author of several books on vaccines, including
Vaccine Safety Manual for Concerned Families and Health Practitioners; Make an Informed Vaccine Decision for the Health of Your Child (with Dr. Mayer Eisenstein); and Vaccines: Are They Really Safe and Effective? Past organizations that he has lectured for include the International Chiropractic Pediatric Association, the International College of Integrative Medicine, Autism One/Generation Rescue, the Hahnemann Academy of North America, and Dr. Gabriel Cousens’ Tree of Life Rejuvenation Center. Mr. Miller is a frequent guest on radio and TV talk shows, has a degree in psychology, and is a member of Mensa

Learn more: http://www.naturalnews.com/038457_vaccine_injuries_infant_deaths_scientific_study.html#ixzz2G3mf3zpw

 

Pesticide companies, not “biotechnology”.

Posted by: admin  /  Category: Health

There are plenty of indications suggesting that the evidence-based paradigm across sciences is built on quicksand, having been largely bought and paid for by many major multinational corporations.

Nowhere is this more evident than in the chemical industry, where pesticide companies posing as “biotechnology” firms specializing in genetics have peddled their wares based on seriously flawed science from the very beginning.

Increasing numbers of scientists are now speaking out in objection to the rampant scientific misconduct muddling the field. Public mistrust in scientists and the corporations that pay them is also on the rise—and rightfully so. Conflicts of interest have become the norm within virtually all fields of science, which creates a completely unworkable situation in the long run.

Our society is largely built on the idea that science can help us make good, solid decisions. But now we’re facing a world so rife with problems caused by the very sciences that were supposed to keep us healthy, safe, and productive, it’s quite clear that we’re heading toward more than one proverbial brick wall.

In a sense, the fundamental role of science itself has been hijacked for selfish gain. Looking back, you can now see that the preferred business model of an industry was created first, followed by “scientific evidence” that supports the established business model.

The injection of industry employees into every conceivable branch of government has led to insanely detrimental health and environmental policies, and the generally accepted idea that scientific integrity is somehow an unassailable fact has allowed the scam to continue for as long as it has. Good old fashioned gangster tactics have also kept the spiel going.

Silencing Scientific Dissent

The featured Corbett Report above and a recent article in The New Yorker1 both discuss the less-than-honorable methods used by industry to silence dissenters—especially scientists whose research doesn’t jibe with preconceived industry decisions.

Corbett discusses the case of Gilles-Eric Séralini and colleagues; French researchers who, in 2012, published the first-ever lifetime feeding study2assessing the health risks of genetically engineered (GE) Roundup Ready corn (NK603). The findings, published in Elsevier’s peer-reviewed journal Food and Chemical Toxicology, were a bombshell.

Rats fed a type of genetically engineered corn that is prevalent in the US food supply for two years developed massive mammary tumors, kidney and liver damage, and other serious health problems, including early death. Some of the tumors weighed in at 25 percent of the rat’s total body weight.

The study was, and still is, among the best evidence of the toxic effects of GE foods. It was also some of the strongest evidence to date that we really need to exercise the precautionary principle and avoid these foods.

The longest industry-led feeding study was 90 days long—a far cry from two years. Of utmost importance, Séralini’s study showed that the major onslaught of diseases really set in during the 13th month of the experiment, although tumors and severe liver and kidney damage did emerge as early as four months in males, and seven months for females.

Still, the industry-funded studies simply didn’t evaluate the health effects of their wares long enough for problems to be detected. And based on that, they’re marketed as safe.

What Séralini’s Research Means in the Big Scheme of Things

The average lifespan of a rat is two to three years. Humans live around 80 years, so we will notice these effects in animals long before we see them in humans. What do you think the effects might be if you feed your child GE foods from day one (yes, many commercial infant formulas even contain GE ingredients) IF the health effects are anything like those found by Séralini?

If 24 months of a rat’s life equates to about 80 years of your child’s, the 13-month mark would be somewhere in your child’s early to mid-40s… GMOs have only been on the market in mass quantities for about a decade. If the effects are as dramatic and as dire as Séralini’s research suggests, then we still have about three decades to go before the jig is up and the effects become apparent, en masse, more or less all at once, in the general population.

GMOs are a long-range gamble, and the pesticide industry is gambling that they won’t have to deal with the fallout once it occurs. Since the publication of Séralini’s 2012 paper, mounting research suggests that glyphosate, the active ingredient in Monsanto’s herbicide Roundup, may be to blame for many of the health problems associated with GE foods, although in the Séralini study, the adverse effects were equally dramatic in rats fed GE maize grown without Roundup.

Study Retracted for No Other Reason Than They Don’t Want It to Be True?

In November 2013, the publisher (Elsevier) retracted the Séralini study saying it “did not meet scientific standards.” However, despite having been reviewed by twice the typical number of referees prior to publication, and having undergone what the publisher called “an intense year-long review” after publication, it wasn’t retracted due to errors, fraud, or even the slightest misrepresentation of data. It was retracted because the publisher deemed the findings inconclusive.

The thing is, inconclusiveness of findings is not a valid ground for retraction.3According to the guidelines for scientific retractions set out by the Committee on Publication Ethics (COPE), the only grounds for a retraction are either clear evidence that the findings are unreliable due to misconduct (data fabrication) or honest error, plagiarism or redundant publication, and/or unethical research.

The reason for the retraction is so ludicrously flimsy, it’s virtually impossible to conclude that Séralini’s paper was retracted for any other reason than the fact that it seriously disrupted the status quo, which is that genetically modified organisms (GMOs) and genetically engineered (GE) foods are safe and nutritionally equivalent to its non-GMO counterparts.

Conflicts of Interest Are Not Even Hidden Anymore

That conflicts of interest have become the norm is evidenced by the fact that industry doesn’t even put much thought into hiding such conflicts anymore. It’s right in your face, and when pointed out, you get little more than a shoulder shrug in response.

In this particular case, we have the curious synchronicity of Richard E. Goodman4 being given a position on Elsevier’s editorial staff shortly prior to the groundless retraction of Séralini’s study. Goodman was a Monsanto scientist for seven years and is an affiliate of the GMO industry-funded group, the International Life Sciences Institute. While Goodman has refuted any involvement in the publisher’s decision to retract this most damaging of all GMO studies, the coincidence seems more than a little convenient. And, regardless of Goodman’s influence, the retraction is quite simply unethical, and undermines the entire scientific process of discovery.

A group of scientists has drafted an open letter requesting Elsevier reverse its retraction of the Séralini paper or face a boycott. The letter may be signed by scientists and non-scientists alike, so please take a moment to sign the letter, and forward it as widely as possible.

Harassment and Other Gangster Tactics

In the featured New Yorker5 article, Rachael Aviv tells the story of Tyrone Hayes,6 whose Atrazine research turned his life into a paranoid nightmare. In the late 1990s, he conducted experiments on the herbicide for its maker, Syngenta. As reported by Aviv:

“…when Hayes discovered that Atrazine might impede the sexual development of frogs, his dealings with Syngenta became strained, and, in November, 2000, he ended his relationship with the company. Hayes continued studying Atrazine on his own, and soon he became convinced that Syngenta representatives were following him to conferences around the world. He worried that the company was orchestrating a campaign to destroy his reputation.”

Two years ago, his work on Atrazine provided the scientific basis for two class-action lawsuits brought against Syngenta by 23 US municipalities, accusing the chemical technology company of contaminating drinking water and “concealing Atrazine’s true dangerous nature.” Documents unearthed during these legal proceedings revealed that Hayes’ suspicions were true—Syngenta had indeed been studying him as deeply as he’d been studying their toxic herbicide for the past 15 years.

What follows reaches a level of creepy that no one should ever have to endure—least of all a scientist who’s working to learn and share the truth about a widely used agricultural chemical that has the power to affect all of us, and our ecology. Aviv writes:

“Syngenta’s public-relations team had drafted a list of four goals. The first was ‘discredit Hayes.’ In a spiral-bound notebook, Syngenta’s communications manager, Sherry Ford, who referred to Hayes by his initials, wrote that the company could ‘prevent citing of TH data by revealing him as noncredible…’ Syngenta looked for ways to ‘exploit Hayes’ faults/problems.’ ‘If TH involved in scandal, enviros will drop him,’ Ford wrote. She observed that Hayes ‘grew up in world (S.C.) that wouldn’t accept him,’ ‘needs adulation,’ ‘doesn’t sleep,’ was ‘scarred for life.’ She wrote, ‘What’s motivating Hayes?—basic question.’”

The Rise of Decision-Based Evidence Making

Ever since the introduction of genetically engineered seeds about 20 years ago, the market for these chemical-dependent crops have spawned a multibillion dollar industry. Funding for the development of more GE crop varieties has come primarily from the privately-owned pesticide industry itself.  Over the last 15 years, conflicts of interest within science have exponentially increased, and at this point, it’s blatantly obvious that financial conflicts of interest play a major role when it comes to what research is done – what gets published, and what doesn’t.

Researchers like Séralini and Hayes are not welcome in a system like this, as the funders of research are really not interested in real science. Their ultimate aim is to use science to further their own agenda, which is to sell patented seeds and chemicals. Studies that cast doubt on the soundness of their business model are simply buried and ignored. Funding plays such an important role in determining the outcome of a study, you’d be wise to investigate who wrote the check before accepting anything you read in the scientific literature. As revealed in a 2011 study published in the journal Food Policy:7

“In a study involving 94 articles selected through objective criteria, it was found that the existence of either financial or professional conflict of interest was associated to study outcomes that cast genetically modified products in a favorable light. While financial conflict of interest alone did not correlate with research results, a strong association was found between author affiliation to industry (professional conflict of interest) and study outcome.”

GMO research in particular is further complicated by the fact that very few independent researchers ever even get the chance to study them, courtesy of strict patent laws. The vast majority of the research done on GMOs is performed by scientists hired by the industry. The results, therefore, are predictable.

Vote with Your Pocketbook, Every Day

 

Remember, the food companies on the left of this graphic spent tens of millions of dollars in the last two labeling campaigns—in California and Washington State—to prevent you from knowing what’s in your food. You can even the score by switching to the brands on the right; all of whom stood behind the I-522 Right to Know campaign. Voting with your pocketbook, at every meal, matters. It makes a huge difference.

I-522 poster
As always, I encourage you to continue educating yourself about genetically engineered foods, and to share what you’ve learned with family and friends. Remember, unless a food is certified organic, you can assume it contains GMO ingredients if it contains sugar from sugar beet, soy, or corn, or any of their derivatives.

If you buy processed food, opt for products bearing the USDA 100% Organic label, as organics do not permit GMOs. You can also print out and use the Non-GMO Shopping Guide, created by the Institute for Responsible Technology. Share it with your friends and family, and post it to your social networks. Alternatively, download their free iPhone application, available in the iTunes store. You can find it by searching for ShopNoGMO in the applications. For more in-depth information, I highly recommend reading the following two books, authored by Jeffrey Smith, the executive director of the Institute for Responsible Technology:

For timely updates, join the Non-GMO Project on Facebook, or follow them on Twitter. Please, do your homework. Together, we have the power to stop the chemical technology industry from destroying our food supply, the future of our children, and the earth as a whole. All we need is about five percent of American shoppers to simply stop buying genetically engineered foods, and the food industry would have to reconsider their source of ingredients—regardless of whether the products bear an actual GMO label or not.

This Salt Is Over 250 Million Years Old..

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If you want your body to function properly, you need holistic salt complete with all-natural elements. Today’s common table salt has nothing in common with natural salt.

Your table salt is actually 97.5% sodium chloride and 2.5% chemicals such as moisture absorbents, and iodine. Dried at over 1,200 degrees Fahrenheit, the excessive heat alters the natural chemical structure of the salt.

This Salt Is Over 250 Million Years Old

Himalayan Crystal Salt

This is by far the purest salt available on earth and is absolutely uncontaminated with any toxins or pollutants.

Once I learned about it and how beneficial it can be for you, my team and I literally spent nearly two years working on having it brought over to the US.

I thought I would be able to provide this salt last year but to say obtaining this salt is difficult would be an enormous understatement. You see, the suppliers of this salt have no standard infrastructure available and we have to work through people that have no idea of how normal business operates.

The shipment had to go through a number of different countries before we were finally able to import it into the US so you can use it.

Quite truthfully, all the bugs are not worked out in the supply system, and we may sell out of this salt very quickly because of all its incredible benefits — that’s why, if you are interested I encourage you to place your order as soon as possible! If we do sell out this supply early, if our past experience is any predictor of the future it may be 6 months to a year before we are able to have more to sell to you. I have never in my life seen a product that has been this challenging to obtain.

This salt from the Himalayas is known as “white gold.” Together with pure spring water, Himalayan Crystal Salt offers all the natural elements exactly identical to the elements in your body — the very same elements originally found existing in the “primal sea.”

Natural Salt Lamp
Get the benefits of Himalayan Salt in a stylish lamp that can accentuate your home or office!
Himalayan Salt Lamps

Containing all of the 84 elements found in your body, the benefits of natural Himalayan Crystal Salt include:

  1. Regulating the water content throughout your body
  2. Promoting healthy pH balance in your cells, particularly your brain cells
  3. Promoting blood sugar health and helping to reduce the signs of aging
  4. Assisting in the generation of hydroelectric energy in cells in your body
  5. Absorption of food particles through your intestinal tract
  6. Supporting respiratory health
  7. Promoting sinus health
  8. Prevention of muscle cramps
  9. Promoting bone strength
  10. Regulating your sleep — it naturally promotes sleep
  11. Supporting your libido
  12. Promoting vascular health
  13. In conjunction with water, it is actually essential for the regulation of your blood pressure

The Typical Table and Cooking Salt in Your
Grocery Store Has Been ‘Chemically Cleaned’

What remains after typical salt is “chemically cleaned” is sodium chloride — an unnatural chemical form of salt that your body recognizes as something completely foreign. This form of salt is in almost every preserved product that you eat. Therefore, when you add more salt to your already salted food, your body receives more salt than it can dispose of.

Salt

This is important as over 90% of the money that people spend on food is for processed food.

Typical table salt crystals are totally isolated from each other. In order for your body to try to metabolize table salt crystals, it must sacrifice tremendous amounts of energy.

Inorganic sodium chloride can keep you from an ideal fluid balance and can overburden your elimination systems.

When your body tries to isolate the excess salt you typically expose it to, water molecules must surround the sodium chloride to break them up into sodium and chloride ions in order to help your body neutralize them. To accomplish this, water is taken from your cells in order to neutralize the unnatural sodium chloride.

This results in a less-than-ideal fluid balance in the cells.

You Are Losing Precious Intracellular Water When You Eat Normal Table Salt

For every gram of sodium chloride that your body cannot get rid of, your body uses 23 times the amount of cell water to neutralize the salt. Eating common table salt causes excess fluid in your body tissue, which can contribute to:

  • Unsightly cellulite
  • Rheumatism, arthritis and gout
  • Kidney and gall bladder stones

When you consider that the average person consumes 4,000 to 6,000 mg of sodium chloride each day, and heavy users can ingest as much as 10,000 mg in a day, it is clear that this is a serious and pervasive issue.

So Why Are Many People Still Using Table Salt?

Because well over 90% of the world’s salt is being used directly for industrial purposes that require pure sodium chloride. The remaining percentage is used for preserving processes and ends up on your kitchen table.

With the use of rigorous advertising, the salt industry is successful in convincing you there are actually health advantages to adding potentially toxic iodine and fluoride to salt. In addition, your table salt very often contains potentially dangerous preservatives. Calcium carbonate, magnesium carbonate, and aluminum hydroxide are often added to improve the ability of table salt to pour. Aluminum is a light alloy that deposits into your brain — a potential cause of Alzheimer’s disease.

Get Salt as Nature Intended It — Pure Himalayan Crystal Salt

Salt
With chemical dumping and toxic oil spills polluting the oceans at an alarming rate, most of today’s sea salt is not nearly as pure as it used to be. Himalayan Crystal Salt is pure salt that is mined and washed by hand — with zero environmental pollutants.

Today’s table and cooking salt is void of the vital trace minerals that make this Himalayan crystal salt so precious. Crystal salt has spent over 250 million years maturing under extreme tectonic pressure, far away from exposure to impurities.

The salt’s unique structure also stores vibrational energy. All of the crystal salt’s inherent minerals and trace elements are available in colloidal form — meaning they are so small your cells can readily absorb them.

The Crystal Salt from the Himalayas does not burden your body as other salts do. It is very difficult for your body to absorb too much crystal salt since there are powerful and effective feedback loops that regulate this process. Natural crystal salt always promotes a healthy balance and does not contribute to high blood pressure like typical table salt.

Crystal Salt’s array of elements forms a compound in which each molecule is inter-connected. The connectedness allows the vibrational component of the 84 trace elements present in the salt to be in harmony with each other and adds to the ability to promote a healthy balance. When it comes to the power of natural salt, nothing compares to Himalayan Crystal Salt. Here’s why:

  • It is the highest grade of natural salt.
  • Under an electron microscope, crystal salt has a perfect crystalline structure.
  • It is mined by hand and hand-washed.
  • Crystal salt is immune to electromagnetic fields
  • Crystal Salt contains no environmental pollutants.
  • There is no limited shelf life and no need for silica packets to prevent clumping.

A New and Different Way to Experience
the Salty-Sweet Goodness of Himalayan Crystal Salt

Himalyan Salt Slab

Not only is Himalayan Crystal Salt far healthier for your body than commercial salt, its taste is unforgettable. Once you try Himalayan salt, I can promise you that you’ll never want to use commercial salt again – I know I don’t.

And here’s a unique way to enjoy Himalayan salt’s slightly sweet-salty goodness with your food…

Featured on several top cooking shows, Himalayan Salt kitchen slabs have become the newest sensation for extraordinary food preparation and presentation.

Measuring a generous 16-1/2 inches by 8 inches, 1-3/4 inch thick and 12.8 pounds, this beautiful translucent pink crystal salt slab serves as a cooking and curing surface, and a lovely way to present chilled foods.

To grill or sauté with your Himalayan Salt Kitchen Slab, simply preheat your slab over a grill or stove and toss on your favorite sliced meats, seafood, vegetables or eggs. The Himalayan crystal salt sears your food to perfection, with a just a light touch of heavenly salty flavor.

Key Minerals in Himalayan Crystal Salt Promote a Healthy Balance in Your Body

Himalayan Crystal Salt is salt in its native form, with all its vibrational energy intact and it helps promote a healthy balance in your body. Promoting balanced electrolytes helps to keep your body in homeostasis — the balance of chemicals that is conducive to the body’s function.

The renowned Frezenius Institute in Europe analyzed the Himalayan Crystal Salt and proved that it has an amazing array of important trace minerals and elements including potassium, calcium and magnesium that help promote a healthy balance by maintaining fluids and replenishing your supply of electrolytes whenever you sweat heavily. (This salt does not supply iodide, a necessary nutrient.)

Himalayan Salt vs. Sea Salt and Rock Salt: A Crystal Comparison

Many people believe sea salt is a healthy alternative to table salt, but this is no longer the case. The oceans are being used as dumping grounds for harmful toxic poisons like mercury, PCBs and dioxin. Reports of oil spills polluting the sea are becoming more frequent. With some 89% of all the sea salt producers now refining their salt, today’s sea salt simply isn’t as healthy as it used to be.

Salt

If you were to look into a microscope at sea salt (pictured left), you would see it has irregular and isolated crystalline structures disconnected from the natural elements surrounding them. Thus, however many vital minerals it may contain, they cannot be absorbed by your body unless the body expends tremendous energy to vitalize them. Your body’s net gain is small compared to the great loss of energy.

Because the crystalline structure of crystal salt is balanced (pictured right), it is not isolated from the 84 inherent mineral elements, but is connected to them in a harmonious state. This means the energy content in the form of minerals can be easily metabolized by your body. When you use this salt, it has a vital energetic effect. Your body gets an ample net gain with little energy loss.

Salt

Mined salt, or rock salt, is also a poor substitute for Himalayan Crystal Salt. While natural rock salt comes close to being intact and is more valuable than industrial table salt, from a biophysical as well as bio-chemical perspective, it holds little value.

The elements contained in rock salt lack sufficient compression to be included in the crystal web, but are only attached to the surface and in the gaps of the crystalline structure. It is the considerable pressure that brings the elements to a colloidal state – where your cells can readily absorb them. The valuable elements found in rock salt are useless because your body cannot absorb and metabolize them.

Crabtree & Evelyn Special..

Posted by: admin  /  Category: Health

 

We are launching our ‘Hand Care Amnesty’ campaign, in which any person can bring in their old hand cream (not a Crabtree & Evelyn one) and trade it for a new Crabtree & Evelyn hand cream, worth £5.00.

T&Cs can be found on the attached image.

 

 

Jamie Rockers
PR & Marketing Administrator, Crabtree & Evelyn (Overseas) Limited
27 Kelso Place, London, W8 5QG, UK
Tel No: +44 (0) 207 361 0477
Fax No: +44 (0) 207 361 0498
Email: [email protected]
Website: www.crabtree-evelyn.co.uk

 

Hand Care Amnesty.pdf

Inorganic calcium is not good for you…

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Calcium…

I want to talk about calcium, not calcium that you are
constantly encouraged to take in an inorganic form but calcium in an organic
form that is helpful, actually, very necessary for a healthy body to function.

Firstly let’s look at the tissue in your body; there are two
types of tissue, healthy and unhealthy. I know which type is more desirable if
given the choice, however, we as 21st century humans are constantly
bombarded by the media to consume a form of calcium that doesn’t have a
positive effect in the body, in fact it has the opposite effect.

The correct form of calcium is a direct supplier of
electrons to the energy factories in our body which are mitochondria, mitochondria
then manufacture the ATP which is then converted into ADP, the necessary
energy, or fuel for the body.

The incorrect calcium, the inorganic or non-biological calcium,
comes in the form of dolomite (rock), bone meal, oyster shell or coral calcium.
This form does not transport electrons so, if anything will work against your
own body and undermine its ability to heal itself

If you watch TV or read magazines, which I suppose 95% of
the population do, you will have seen commercials or advertisements for calcium
in one form or another. In the main, these commercials and ads promote calcium
in a contaminated form. This cannot carry electrons as they have been altered
by the food industry, I’m not saying they have done this to harm you, but it’s
been done to enable their product to have a longer shelf life or has been
diluted of its active nutritional benefits.

When working for Dr Huggins, I regularly talked with clients
boasting of how many supplements they consumed every day. Most would tell me
about the calcium they took but also complained because they were still very
unhealthy. This only emphasized that just taking supplements, without knowing
specifically what your body needs is not the right thing to do. There is only
one way of knowing this, in my humble opinion, and that is to have your blood
tested and the results interpreted by someone that understands body chemistry.
That being said my recommendation is to call Huggins Applied Healing and use
the Assist program, this way your chemistry’s would be analyzed. You will
receive a 120 page document detailing the imbalance in your chemistry’s and
most importantly, how to address this imbalance.

I must point out that at this time I have no connection
physically or financially to Huggins Applied Healing: The above is purely my
opinion based on the more than three years of working for Dr Huggins.

If you are appreciating my work, then consider subscribing to my monthly newsletter for only $3.50 per month. Not only will you find more up to date information on the subject of health but you will be making a contribution to the operation that will restore my health.

Replacement’s…

Posted by: admin  /  Category: Health

Dentures…

I’m sure the thought of dentures to a lot of people is quite worrying, having teeth removed and then having a lump of plastic in your mouth strikes fear into your heart. Well, you have to consider the long term implications, rather than the narrow minded short term view of “how you look” or “what will others think”.

Options like Implants or Root canals may look nicer to an observer but will create long term problems for you, remember those people looking at you, do not live in your body, they do not have to cope with the pain and heartache of disease and illness. So many people contract a serious and often life threatening disease when they have had those artificial things permanently placed into their body.

Your body doesn’t want artificial things permanently placed into it, your immune system will do the job it’s meant to and that is to find unnatural or non self cells and attack them, try to eliminate them and remove them from the temple it calls your body.

So a denture, be it partial or full is definitely a better option, it’s healthier in so many ways, you can take it out of you mouth daily and clean it, clean under it and remove bacteria.

When I was working for Dr Huggins I regularly spoke with people asking a question about dentures, I would do my best to reassure them that dentures are a good option. However please read the article on cavitation’s and how to avoid them before having teeth removed.

You will often be told that the denture will be made to look a similar color to your gums, less offensive and less obvious, actually that is a load of BS so don’t let them do that.

The denture should have the minimal coloring as possible, when it’s colored pink, it is very obvious but there is a bigger factor involved, and that is the coloring agent’s used.

When it is colored pink, the color is made from either mercury or cadmium or both, I’ve said this many times before and I’m sure I’ll say it hundreds of times more. Mercury is the most toxic non radioactive substance on earth, Cadmium is not far behind. So steering clear of both is a good option.

The denture should be made from Clear Acrylic, nearly three years ago I had to have a 6 tooth partial because I had my front six teeth removed. Yes, I was really worried about having it done, but I was lucky to be able to see one of the best dentist’s in the country and probably the best in terms of Huggins trained dentists, Dr Blanche Grube who I honestly believe I owe my life to.

Rest assured, an implant or root canal is a horrible long term thing to have in your mouth, millions of people have contracted a disease or illness since having them, do they realize that this is the reason they became sick? no they don’t understand that. This is because there are billion and trillion dollar organizations spending millions of dollars on advertising to persuade, confuse, brainwash then reassure the public that these artificial things are friendly to the human body.

I ask you this question which I’d like you to spend a little time thinking about: why is this nation, the most powerful nation in the world, in the bottom half of the sickest nations in the world. Look at statistic’s compiled by the World Health Organization, the last time I looked the USA was number 90 in the list of 174 countries.

Our health is only important to ourselves and our loved ones, big pharma and the other five organizations that make up the group of six that control this country, do not give a hoot. They know that in their long term plan of reducing the population of the world and becoming more and more wealthy in the process is all that matters.

Half of All Dentists Still Use Mercury Amalgam?

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Banned for Pets and Farm Animals, but Okay for You and Your Children?

By Dr. Mercola

With Consumers for Dental Choice

Dental amalgams have been in use since the American Civil War. They are an anachronism that has been perpetuated by dental industry patents, and there’s a conspiracy of silence that seeks to keep the 75 percent of Americans who are ignorant about that fact that amalgam fillings are actually 50 percent mercury.

As stated by Charlie Brown, who founded the Consumers for Dental Choice in 1996:

“The only way amalgam could be marketed was to hide the mercury. The only way you could hide the mercury is to have a coordinated effort to make sure that nobody blew the whistle.

At the start of our movement, we confronted an iron triangle; three major forces: The American Dental Association that profit from a system of consumer ignorance; The Food and Drug Administration that sits in the hip pocket of the American Dental Association… and the state dental boards, who were the enforcers who told dentists, “You have to be silent.”

The American Dental Association had a gag rule and said, “Don’t say the M word. Don’t tell people about the mercury; don’t say that it’s toxin, or there will be consequences.” The consequences were the state dental boards pulling licenses of dentists all through the 1990s and threatening to pull the licenses of many more.

Fortunately in the last 10 years nearly half of all US dentists have recognized the dangers of amalgams and have stopped using them in their practice. But the remaining 50 percent of dentists still use them, and that currently accounts for between 240-300 tons of mercury entering the market every year. In the United States, dental offices are the second largest user of mercury – and this mercury eventually ends up in our environment by one pathway or another.

Did You Know?…

Dental amalgam can cause far-reaching problems, such as:

Exposure to mercury, the most toxic and more vaporous of the heavy metals, can harm your kidneys, and permanently damage your child’s developing neurological system, and even kill your unborn child in the womb.

To implant amalgam, a dentist drills out healthy tooth matter in order to carve the crater necessary for amalgam placement – a primitive process that irreversibly weakens tooth structure. With a damaged tooth structure and with a metal-based filling that expands and contracts with temperature changes, teeth with amalgam are much more likely to crack years later, necessitating additional dental work.

Amalgam is a workplace hazard, especially for young female dental workers who experience an elevated rate of reproductive failures.

Dental mercury is the number one source of mercury in our wastewater, so dentists are handing the clean-up bill for their pollution to taxpayers and water ratepayers.

Why would a primitive, pre-Civil War polluting product that is 50 percent mercury and cracks teeth still be going into your mouth?

Amalgam was introduced in the Civil War era by the new American Dental Association, which won a political battle with the physicians of the mouth, who said using mercury in oral health care is malpractice. Florida dentist James Hardy, in his book Mercury Free, refers to the creation of amalgam and the creation of the American Dental Association as the “twin-birth.”

Why Do Half of All Dentists Still Use Mercury Amalgam?

We now know the risks, so why do half of dentists continue to use the filling material used by their great-grandfathers?

Is it the price?

No.

The alternatives to amalgam are comparably priced – or even less expensive. Amalgams cost more than glass ionomers, which can be applied via a mercury-free technique called Atraumatic Restorative Treatment (ART). ART does not require drilling; only hand instruments, and is virtually painless.

Amalgam also cost the same as composite fillings (also called resin) for smaller cavities, although composite can cost a few bucks more for large cavities. But when you add the horrid environmental and health catastrophe caused by amalgam, of course, amalgam’s cost to society is much higher…

The answer is: Profits!

Amalgams are quick and easy. Dentists make more money per chair per day implanting mercury. For factory-style dentistry, where the teeth represent dollar signs instead of part of a human being, dentists drill, fill, and bill. The term “drill, fill, and bill” is a joke aspiring dentists learn in dental school. Only the joke is on us and our children: they count their money, and we have a vaporous neurotoxin implanted an inch from our brains or our children’s brains.

And of course, since amalgam damages tooth structure and cracks teeth, pro-mercury dentists will continue to profit from amalgam long after its initial placement. Teeth with amalgam require more dental work in the long term. So for the pro-mercury half of dentists, amalgam is the gift that keeps on giving.

How Can Pro-Mercury Dentists Compete with Toxic-Free Dentists?

The pro-mercury dentists’ trade group, the American Dental Association, has pulled every lever with Congress, the Food and Drug Administration, the state dental boards and the corporate media to cover up amalgam’s mercury.

First, the ADA popularized the deceptive term “silver fillings,” so consumers would think amalgam is made mainly of silver (actually, it has twice as much mercury as silver).

Second, it mounted a no-holds-barred campaign to silence competitors and critics of 19th century dentistry, especially the courageous dentists who realized their leadership was so fundamentally in error.

According to its own self-description, the American Dental Association appears focused more on promoting products – and getting paid handsomely to do so – than in promoting its dentist members. At the bottom of its news releases, the ADA has frequently written:

“The not-for-profit ADA is the nation’s largest dental association, representing more than 155,000 dentist members. The premier source of oral health information, the ADA has advocated for the public’s health and promoted the art and science of dentistry since 1859. The ADA’s state-of-the-art research facilities develop and test dental products and materials that have advanced the practice of dentistry and made the patient experience more positive. The ADA Seal of Acceptance long has been a valuable and respected guide to consumer and professional products. For more information about the ADA, visit the Association’s Web site at www.ada.org.”

Of the five sentences, one is about members, and three about the ADA’s product endorsement system. The “ADA Seal of Acceptance” is a pay-to-play system in which companies pay the ADA to secure their endorsement. By contrast, the American Medical Association will not do pay-to-play endorsements of products; it is considered unethical.

The ADA owns two patents on amalgam, patent numbers 4,018,600 and 4,078,921. They have expired, but

while they were in effect the ADA went to incredible lengths to wipe out mercury-free dentistry and quash dissent from the emerging critics of mercury-based dentistry.

The Role of the American Dental Association

How does the ADA keep pro-mercury dentists in business – and keep profits rolling in for the amalgam makers?

Here’s how:

The “silver fillings” deceptionGold fillings are called gold because they are made of gold. Seizing on the comparison, the ADA brochures promoting mercury fillings called them “silver fillings.” The ADA claims the term means “silver-colored,” but who are they fooling? In my dictionary, the first definition of “silver” is the element. The color is the fourth definition, behind the element, medium of exchange, coins, and eating utensils.Consumers for Dental Choice, with its Campaign for Mercury-Free Dentistry, fought back against the “silver fillings” deception. In California these advocates launched the term “say the M word,” which led to fact sheets on amalgam in that state and several other states and cities. These fact sheets, which dentists are required to hand their patients, inform the public that amalgam is mercury.

The gag ruleWhen its amalgam patents were in effect, the ADA used its power to block the emergence of mercury-free dentistry by adopting a rule of conduct prohibiting dentists from discussing mercury with their patients:

“Based on available scientific data, the ADA has determined that the removal of amalgam restorations from the non-allergic patient for the alleged purpose of removing toxic substances from the body, when such treatment is performed solely at the recommendation or suggestion of the dentist, is improper and unethical.”

Yes, the ADA said it is unethical for a dentist to tell the truth to his patients!

Thanks to an extraordinary campaign by Consumers for Dental Choice, the gag rule is now just about defunct. Working with state lawmakers, with civil liberties organizations, with state Attorneys General (Charlie Brown, head of the consumer group, used to be one), and with an outraged citizenry, the movement for Mercury-Free Dentistry succeeded in the legislatures, in the courts, and in the courts of public opinions to restore free speech rights to dentists.

Rent-a-CongressmanHow about the political process? We do have friends in Congress, Republicans like Congressman Dan Burton and Senator Mike Enzi, and Democrats like Congressman Dennis Kucinich and Congressman Gregory Meeks. But they are few and far between.The ADA has been particularly devious in the halls of Congress. It doesn’t instruct its minions in Congress – members from both political parties – to write bills, conduct hearings, nor even make speeches. Instead, the ADA buys silence and inaction from Members of Congress. Sound familiar? It was the same tactic used by Big Tobacco for several decades.At the state level, it’s the same; in some state capitals, the ADA has had the single largest political action committee. The tactic is the same: Do nothing, say nothing, and cash the PAC money.

Strong-arming the children of AmericaIn the Maine legislature, money is not king. The state has fair practices that limit outside money and create a level-playing field for unfunded candidates. Unable to buy their way into power, the ADA resorted to outright strong-arming. A bill was gaining momentum in the Maine Legislature to phase out amalgam. The ADA struck back, threatening to deny treatment for Maine children if their dentists could not use their favorite filling material. If amalgam were banned, the ADA threatened:

“The result will be treatment delayed, treatment denied, and treatment never being

sought. That is not a situation the dentists of Maine, the United States, or our policymakers can be willing to accept.”

Several years later, the ADA’s Pennsylvania chapter pulled the same power play against children with disabilities. A fact sheet law in the City of Philadelphia meant parents are now made aware of amalgam’s horrid health risks to their children. In inner-city clinics, parents were insisting on mercury-free dentistry – the same as parents do in the affluent areas. But to the Pennsylvania Dental Association, inner-city parents were supposed to take the crumbs their dentists offered: mercury fillings or no fillings.

A dental association leader was demanding that parents of children with disabilities sign a release allowing him to put mercury fillings in their children; when they refused, he denied all treatment. No tooth cleanings. Nothing… Suburban parents might go to a dentist down the street, but for inner-city minority parents of children with disabilities, finding a dentist is not easy – and this dentist knew it. Incredibly, the Pennsylvania Dental Association – which claims to support choice for children in the suburbs – endorsed the position of this dentist.

Fortunately, the story did not end there. This callous power play endorsed by the Pennsylvania Dental Association – denying dental care for children with disabilities unless they agreed to mercury fillings – caught the attention of the disability rights community. The Pennsylvania Governor’s Advisory Commission on Disabilities enacted a resolution condemning this ADA chapter.

What Can You Do to Stop the Use of Amalgam?

During this Mercury-Free Dentistry Awareness Week, I urge you to help spread the word and help educate others by sharing this article with your social networks. Together, we can END the use of toxic mercury in dentistry.

Charlie Brown, who runs Consumers for Dental Choice, is headed to Nairobi in October to lead a worldwide delegation participating in the world mercury treaty negotiations. With him will be a team of dentists, consumers, attorneys, and scientists fighting to get amalgam into that treaty. With the world deciding whether we continue allowing mercury in children’s mouths, much is at stake. Here’s what you can do in your nation or state:

Americans: Our #1 problem is the Food and Drug Administration, which has partnered with the American Dental Association to cover up the mercury, to make you think you are getting silver instead of mercury in your mouth. The FDA intentionally conceals the warnings about amalgam deep in its regulation — so parents will never see them. On its website, the FDA gives dentists the green light to continue to deceive consumers

with the term “silver fillings”

“Americans are ready for the end of amalgam.” This was the theme of the testimony to the U.S. Department of State on August 18 by former West Virginia state Senator Charlotte Pritt. Yes, Americans are ready. But FDA is not. So let’s send them a message.

Nine months ago, FDA scientists advised the agency to disclose the mercury to all patients and parents, and to stop amalgam for children and pregnant women. Yet FDA sits – sits actually in the pocket of the American Dental Association – ignoring its own scientists.

Please write the Director of FDA’s Center for Devices, Jeff Shuren, [email protected] Ask Dr Shuren why FDA continues to ignore the scientists and covers up the mercury from American parents and consumers. Ask when FDA is going to get in step with the world on mercury.

Dr. Jeff Shuren, Director
Center for Devices, U.S. Food & Drug Admin.
10903 New Hampshire Ave.
WO66-5431, Room 5442
Silver Spring, MD 20993-0002
Telephone: 301-796-5900
Fax: 301-847-8149
Fax: 301-847-8109

Californians: Dr. Shuren is coming to San Francisco for a “town meeting” on September 22. We urge Northern Californians to attend. It will go from 8 am to 12 noon, at the Embassy Suites Hotel, San Francisco Airport (telephone 650.589.3400)

In Southern California, Consumers for Dental Choice is organizing a city-by-city attack on amalgam — and needs volunteers. If you wish to help with the grassroots work of organizing for city council hearings, gathering petitions, and telephoning, volunteer by writing [email protected]

Australians: Your government, Aussies, is now in last place on the mercury treaty, asking the world to throw in the towel instead of working to phase out dental mercury. A great new group has started, Australians for Mercury-Free Dentistry, led by dentist Lisa Matriste and consumer activist Anna Priest. We urge you to go to its website and join: http://www.mercuryfreedentistry.com.au/

Folks worldwide: If you aren’t on that list, there’s plenty to do – for example, Dominique Bally, an outstanding young advocate from the Ivory Coast, runs the Amalgam-Free Africa Campaign. If you want to help somewhere, anywhere, and there’s nothing on the list above for you, write Charlie Brown, [email protected]

Consumers for Dental Choice is working to protect your health – and the health of your children – all around the world. Charged with this important mission at state and local, national, and international levels, Consumers for Dental Choice would appreciate your help!

Dr. Mercola Recommends…

FDA…Big pharma’s pawn…

Posted by: admin  /  Category: Health

 

According to the FDA itself, drug companies provide fully 60% of the FDA’s drug review costs

FDA “Negotiating” to Get More Money from Big Pharma—Again!

September 13, 2011

Increasingly Pharma is funding the FDA. No wonder the agency seems to dance to their tune.

The Prescription Drug User Fee Act (PDUFA) authorizes the FDA to collect fees from companies, allegedly to fund and expedite the drug approval process, but really to pay the agency’s bills. Under this authority, pharmaceutical companies pay fees for certain new human drug applications, biologics applications, and supplements submitted to the agency for review—and the FDA’s review of an application cannot begin until the fee has been submitted.

The law was enacted in 1992, and Congress needs to renew it every ten years; the next deadline for renewal is September 2012. To make this happen, the FDA has been performing its usual ritual of begging and blustering at the same time.

The FDA has been discussing a raise in the FDA “user” fees with industry since July 2010; in fact, Big Pharma had already agreed to a 6% increase in fees for new drugs through 2017. The increase is expected to produce an additional $40.4 million in user fee revenue in fiscal 2012, bringing the fiscal 2013 total to $712.8 million. But FDA still hasn’t arrived at a deal with companies on user fees for medical devices—the FDA made a proposal, but industry rejected it, so the negotiations continue.

According to the FDA itself, drug companies provide fully 60% of the FDA’s drug review costs—which means that the FDA’s review and regulation of pharmaceutical drugs is largely funded by the very drug companies under review!

Could this brand of crony capitalism be part of the reason why the FDA is apparently so biased against supplements, which it regards as competition for drugs? Or why the drugs the FDA approves are so dangerous that, as we reported last year, they kill 50,000 Americans and send more than 700,000 more to emergency rooms each year?

PDUFA is what is known as a “must-pass” bill. Such bills become vehicles for other, smaller bills looking to slide through unnoticed as riders. We will keep a close watch on that—as well as on the FDA’s so-called negotiations with its friends in the pharmaceutical industry.