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Election Season 2014

And it has brought us to this trainwreck called ObamaCare and we have bankrupted our kids and grandkids!

We are now headed into the 2014 Election Season and common sense and conservatism are on the rise. Please stand-up and be counted!

Reading Collusion: How the Media Stole the 2012 Election is a great place to start!

The Founding Father's Real Reason for the Second Amendment

And remember the words of Thomas Jefferson "The strongest reason for the people to retain the right to keep and bear arms is, as a last resort, to protect themselves against tyranny in government." See Video of Suzanna Gratia-Hupp’s Congressional Testimony: What the Second Amendment is REALLY For, below (u-tube HERE).

The Leaders Are Here... Palin, Cruz, Lee, Paul, Chaffetz....

T'S A WONDERFUL LIFE

Can You Really Still Believe That None of These People Would Have Done a Better Job???

Bloggers' Rights at EFF

SIGN THE PETITION TODAY...

Showing posts with label FDA. Show all posts
Showing posts with label FDA. Show all posts

Sunday, April 29, 2012

Pathological Politics – Predatory Partners and Persecuting Patriots

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By: Terresa Monroe-Hamilton - the NoisyRoom

In the notorious tradition of Nixon’s Enemies List, Obama is now openly persecuting patriots at every opportunity. He tries to shame them, taint them, marginalize them and if all that doesn’t work, he sends goons after them and either imprisons them or threatens them with imprisonment. He’s using every agency at his disposal, with a special emphasis on the EPA, FDA, IRS, SEC, ATF and Fish and Wildlife authorities. And he has hired a whole governmental ‘army’ to enforce his dictates and go after his enemies. Welcome to the American Stasi.

We have watched how Obama smears those who would dare to donate to Mitt Romney’s campaign. That should make us want to donate even more, not back down and cower in fear. We all know that Obama is determined to be reelected legally or illegally – he doesn’t care. He just wants to hold on to his power, so he can finish what he started – destroying America with his pathological politics of corruption, greed and evil. If the elections don’t suffice, he’ll invent an emergency to ensure his death grip on the throat of America.

Look at how Gibson Guitars has been treated. They have been raided multiple times, but they can’t defend themselves because in the last three years, this administration won’t say what crime they are charging them with. They are destroying a good and honest company that creates jobs and does business production here in America. Their crime – successful capitalism. Something Obama will not tolerate.

Then there are farmers. The EPA is clamping down on the Amish and others who don’t follow every regulation in an effort to put them out of business and it is working. I hear the stealthy, sly footsteps of Cass Sunstein. Soon, very soon, the government will control all our farmland and food. Then if you step out of line, they’ll just starve you to death. Farming on your own property will be illegal. It’s coming – bet on it. Right now they are seizing farmer’s bank accounts. The FDA is now using the terrorist based “Bank Secrecy Act” as justification to invade, investigate and even confiscate the bank accounts of Americans in the agricultural business.

From The Examiner:

The Bank Secrecy Act that came out of the events of 9/11, which has been expanded during the decade long war on terror, is now being used to criminally attack farmers who choose not to use banks as their sole or primary source for monetary transactions. This is especially relevant after the credit crisis of 2008, where many American[s] began withdrawing money from banks after bank solvency came into question.

This banking law, which allows for the unwarranted confiscation and seizure of funds based solely on perceived impropriety, is one of many new policies created under the Bush and Obama administrations to control the public, and the flow of money in the United States. Beginning in 2013, new capital controls are set to be implemented which will make it extremely difficult to move dollars in and out of the country, and more recently, the Obama administration diverted funds from other departments to hire thousands of IRS agents for the new healthcare system that will also commence in 2013.

Ted Nugent on Regulations

Glenn Beck – We Are All Criminals Now

Now, we turn to Ted Nugent, who has been all over the news as of late. Evidently Obama has had Ted Nugent in his sights for at least two years and probably much longer. Nugent was charged with breaking a law – of which the judge hadn’t even heard – while hunting black bear in Alaska. But you can bet the Feds did and they brought charges hoping to snare Nugent. But that didn’t work out as they intended – Nugent accepted that he ‘unknowingly’ broke the law and the sentence carried the same weight as jaywalking, a misdemeanor offense. They tried to snag him in California and accused him of baiting a deer. A total falsehood and you’d have to be a moron to do it since he was airing the episode on TV. They stormed three of his friends’ homes and then searched a room not covered by the search warrant. They found a set of brass knuckles and told Nugent’s friend they would drop the felony charge if he would help them ‘get’ Nugent. Fortunately Ted has very good friends. But they took all kinds of stuff from their homes.

Now, they have made Nugent slaughter his pigs in Michigan – labeling them as feral. Since when is livestock you keep in a pen ‘feral?’ Obviously they either don’t know or more likely, don’t care what the definition is. They were the wrong color and thus deemed ‘feral’ and Nugent was forced to slaughter them. It’s tempting to draw conclusions about motives related to winning points with the Dearbornistan locals, given that the “reason” for slaughtering the pigs is clearly a pretext; one wonders to oneself, could squeezing pig farmers be calibrated to curry favor with a Muslim community?

He’s also been persecuted for his Oryx in Texas as well. They are harassing him about raising these animals when he brought them back from the brink of extinction. A three legged little one was born and he is not being allowed to put it out of its misery. It will die a slow and painful death. How is that compassion? If he puts it down, it’s a felony.

Someone high up would not allow Nugent to attend a SEAL’s funeral when it was the hero’s final wish. His concerts have been cancelled in several cases as well. The Feds interviewed him over comments he made at an NRA conference recently. He was cleared, but I guess free speech is no longer very ‘free’ in this country. Nugent is a good man – a patriotic man. That’s a lot more than you can say about Obama and his thugs.

This isn’t just about Ted Nugent folks – it’s about each and every one of us. They are coming after the bloggers, the patriots, small businesses, you name it. There is no way we can avoid violating one of these bogus laws. It’s only a matter of time. Obama doesn’t care about the Constitution – it means nothing to him. They are coming and we had better stand together, or we will all hang separately as patriots. The way Nugent is being treated is absolutely disgraceful.

From Kim Strassel at the Wall Street Journal:

He’s targeted insurers, oil firms and Wall Street—letting it be known that those who oppose his policies might face political or legislative retribution. He lectured the Supreme Court for giving companies more free speech and (falsely) accused the Chamber of Commerce of using foreign money to bankroll U.S. elections. The White House even ginned up an executive order (yet to be released) to require companies to list political donations as a condition of bidding for government contracts. Companies could bid but lose out for donating to Republicans. Or they could quit donating to the GOP—Mr. Obama’s real aim.

We all know of Obama’s Enemies List, but do you know who his predatory partners are? Along with Communists and radicals, he has a special fondness for the Muslim Brotherhood. In fact, he has opened the front door of the White House and has told them to make themselves at home. These are the evil asshats who support and fund Hamas. These are Islamic terrorists of the ilk that carried out 9-11 and Obama embraces them while persecuting American patriots.

Rumors of War III

Obama is not even subtle about it. They have removed all references to radical Islam in federal publications. They allow Shariah Law to be carried out on American soil. Obama’s best friend is the Prime Minister of Turkey who gives him advice on his daughters. You see, it doesn’t matter whether Obama is a Muslim or not, his father was. Obama has Islamic street cred. It even gives him a basis for using Taqiyya against Americans. Obama is actively and aggressively promoting Islam around the planet and especially here at home. The only thing that matches his love of Islam, is his hatred of Israel.

If one is known by who his friends and enemies are, then Obama’s predatory partners and the patriots he persecutes are screaming volumes at us. It’s clear that his campaign of pathological politics and communism is on a set of tracks that leads somewhere we dare not go.

Friday, November 26, 2010

Dumbing Down Society Part I: Foods, Beverages and Meds

It will only get worse with the passing of S.510  -Contact your Senator(s) and insist they vote NO!!

Link to:  S.510: FDA Food Safety Modernization Act

“If accepted, [S 510] would preclude the public’s right to grow, own, trade, transport, share, feed and eat each and every food that nature makes. It will become the most offensive authority against the cultivation, trade and consumption of food and agricultural products of one’s choice. It will be unconstitutional and contrary to natural law or, if you like, the will of God.” ~ Dr. Shiv Chopra, Canada Health Whistleblower.

Dumbing Down Society I:  Foods, Beverages and Meds

By Vigilant | Originally Posted June 28th, 2010 |  Vigilant Reports |

Is there a deliberate effort by the government to dumb down the masses? The statement is hard to prove but there exists a great amount of data proving that the ruling elite not only tolerates, but effectively introduces policies that have a detrimental effect on the physical and mental health of the population. This series of articles looks at the many ways the modern man is being dumbed down. Part I looks at the poisons found in everyday foods, beverages and medications.

The theme of dumbing-down and dehumanizing the masses are often discussed in articles on The Vigilant Citizen. The presence of those concepts in popular culture are, however, only the outward and symbolic expression of the profound transformation happening in our society. Scientific data has been proving for years that governments around the world are tolerating the selling of many products which have a direct and negative effect on cognitive and physical health. As we will see in this article many everyday products cause brain damage, impaired judgment and even a lower IQ.

Is a dumber population something that is desired by the elite? Hitler once said “How fortunate for the leaders that men do not think.” An educated population knows its rights, understands the issues and takes action when it does not approve of what is going on. Judging by the incredible amount of data available on the subject, it seems that the elite want the exact opposite: an unhealthy, frightened, confused and sedated population. We will look at the effects of medication, pesticides, fluoride and aspartame on the human body and how those products are being pushed by people from inside the power structure.

Prescription Drug Abuse

America has witnessed during the last decades a staggering rise of drugs being prescribed  to treat all kinds of problems. Children are particularly affected by this phenomenon. Since the 1990′s, an ever-rising proportion of American children are being diagnosed with “illnesses” such as Attention Deficit Disorder (ADD) and are prescribed mind-altering drugs, such as Ritalin.

The DEA has become alarmed by the tremendous increase in the prescribing of these drugs in recent years. Since 1990, prescriptions for methylphenidate have increased by 500 percent, while prescriptions for amphetamine for the same purpose have increased 400 percent. Now we see a situation in which from seven to ten percent of the nation’s boys are on these drugs at some point as well as a rising percentage of girls.  - Source

Today, children who show too much energy, character or strength are being willfully sedated with powerful drugs which directly affect the way their brains function. Are we going in the right direction here?

Even if ADD is not a clearly defined and documented disorder – it causes NO observable biological effects whatsoever – children are still being diagnosed with the illness in great numbers. This raises important ethical questions.

“Pediatricians as well as ethicists have also voiced their concerns in usage of these stimulants. In an article published in the New York Times, they have questioned the appropriateness of medicating children without a clear diagnosis in hopes that they do better in school. They also asked whether the drugs should be given to adults failing in their careers or are procrastinators. They question the worthy of this method.

This concern have also been voiced out in the January 2005 issue of Pediatrics in which the large discrepancies between pediatricians’ practice patterns and the American Academy of Pediatrics (AAP) guidelines for the assessment and treatment of children with attention-deficit/hyperactivity disorder (ADHD) was bought forth. The article also stated that because the medical community didn’t come to a consensus on how to diagnose ADD/ADHD, they should not be making extensive decisions as to how to treat individuals who have been diagnosed with the disorder.”

The usage of Ritalin at a young age breaks the psychological threshold people maintain towards the usage of prescription pills, which makes those children more likely to consume psychotropic drugs later in their lives. We should not be surprised to witness a dramatic increase of consumption of antidepressants in the years to come. The trend is already beginning:

“In its study, the U.S. Centers for Disease Control and Prevention looked at 2.4 billion drugs prescribed in visits to doctors and hospitals in 2005. Of those, 118 million were for antidepressants.

The use of antidepressants and other psychotropic drugs — those that affect brain chemistry — has skyrocketed over the last decade. Adult use of antidepressants almost tripled between the periods 1988-1994 and 1999-2000. Between 1995 and 2002, the most recent year for which statistics are available, the use of these drugs rose 48 percent, the CDC reported.”   - Elizabeth Cohen, CNN

The use of prescription pills might be of a great help for specific and properly diagnosed cases. The pharmaceutical industry however, which has many “friends” in the highest levels of government, is pushing for the widespread use of psychiatric drugs within the public. Since 2002, a great number of pills claiming to fix all kinds of mental conditions have been marketed to the public, but many of those pills were approved for sale without proper research for side effects. Even worse: the side effects might have been known but hidden to the public. Below is a list of warnings issued on commonly sold psychiatric drugs. Some of those side effects are actually frightening as a pill should not be able to have that much power over the human brain. Think about it: Some drugs are subject to warnings because they can cause you to … commit suicide?

2004

March 22: The Food and Drug Administration (FDA) warned that Prozac-like antidepressants (called Selective Serotonin Reuptake Inhibitors or SSRIs) could cause “anxiety, agitation, panic attacks, insomnia, irritability, hostility, impulsivity, akathisia [severe restlessness], hypomania [abnormal excitement] and mania [psychosis characterized by exalted feelings, delusions of grandeur].”

June: The Therapeutic Goods Administration, the Australian equivalent of the FDA, reported that the latest antipsychotic drugs could increase the risk of diabetes.

June: The FDA ordered that the packaging for the stimulant Adderall include a warning about sudden cardiovascular deaths, especially in children with underlying heart disease.

October 15: The FDA ordered its strongest “black box” label for antidepressants warning they could cause suicidal thoughts and actions in under those under 18 years old.

October 21: The New Zealand Medicines Adverse Reactions Committee recommended that older and newer antidepressants not be administered to patients less than 18 years of age because of the risk of suicide.

December 17: The FDA required packaging for the “ADHD” drug, Strattera, to advise that “Severe liver damage may progress to liver failure resulting in death or the need for a liver transplant in a small percentage of patients.”

2005

February 9: Health Canada, the Canadian counterpart of the FDA, suspended marketing of Adderall XR (Extended Release, given once a day) due to reports of 20 sudden unexplained deaths (14 in children) and 12 strokes (2 in children).

April 11: The FDA warned that antipsychotic drug use in elderly patients could increase the risk of death.

June 28: The FDA announced its intention to make labeling changes to Concerta and other Ritalin products to include the side effects: “visual hallucinations, suicidal ideation [ideas], psychotic behavior, as well as aggression or violent behavior.”

June 30: The FDA warned that the antidepressant Cymbalta could increase suicidal thinking or behavior in pediatric patients taking it.  It also warned about the potential increased risk of suicidal behavior in adults taking antidepressants.

August: The Australian Therapeutic Goods Administration found a relationship between antidepressants and suicidality, akathisia (severe restlessness), agitation, nervousness and anxiety in adults.  Similar symptoms could occur during withdrawal from the drugs, it determined.

August 19: The European Medicines Agency’s Committee for Medicinal Products warned against child antidepressant use, stating that the drugs caused suicide attempts and thoughts, aggression, hostility, aggression, oppositional behavior and anger.

September 26: The Agenzia Italiana del Farmaco (Italian Drug Agency, equivalent to the FDA) warned against use of older (tricyclic) antidepressants in people under 18 years old.  It also determined the drugs were associated with heart attacks in people of any age.

September 29: The FDA ordered that labeling for the “ADHD” drug Strattera include a boxed warning about the increased risk of suicidal thinking in children and adolescents taking it.

October 17: The FDA warned that the antidepressant Cymbalta could cause liver damage.

October 24: The FDA withdrew the stimulant Cylert from the market because of the risk of liver toxicity and failure.

November: The FDA warned that the antidepressant Effexor could cause homicidal thoughts.

2006

February 9: The FDA’s Drug Safety and Risk Management Advisory Committee urged that the strongest “black box” warning be issued for stimulants, because they may cause heart attacks, strokes and sudden death.

February 20: British authorities warned that Strattera was associated with seizures and potentially lengthening period of the time between heartbeats.

March 22: An FDA advisory panel heard evidence of almost 1,000 reports of kids experiencing psychosis or mania while taking stimulants.

May 3: FDA adverse drug reaction reports linked antipsychotic drugs to 45 child deaths and 1,300 serious adverse reactions, such as convulsions and low white blood cell count.

May 12: The manufacturer of Paxil warned that the antidepressant increases the risk of suicide in adults.

May 26: Health Canada issued new warnings of rare heart risks for all drugs prescribed for “ADHD,” including the risk of sudden death.

June 2: An FDA study determined that the antipsychotic drug, Risperdal, might cause pituitary tumors. The pituitary gland, at the base of the brain, secretes hormones that promote growth, and regulates body functions.  Antipsychotics may increase prolactin, a hormone in the pituitary gland, and this increase has been linked to cancer.  Risperdal was found to increase prolactin levels more frequently than in other antipsychotics.

July 19: The FDA said antidepressant packaging should carry warnings that they may cause a fatal lung condition in newborns whose mothers took SSRI antidepressants during pregnancy.  Migraine sufferers also need to be warned that combining migraine drugs with SSRIs could result in a life-threatening condition called serotonin syndrome.

Food Poisoning

The modern man ingests in his lifetime an incredible amount of chemicals, artificial flavors and additives. Although there is growing awareness regarding healthy eating, there is also a lot of misinformation and disinformation.

At the present time, a single company – Monsanto – produces roughly 95% of all soybeans and 80% of all corn in the US. Considering this, the corn flakes you had for breakfast, soda you drank at lunch and beefstew you ate for dinner likely were produced from crops grown with Monsanto’s patented genes. There are numerous documents and films exposing Monsanto’s strong-arming of the agricultural industry, so I won’t expand on that issue. It is however important to note that a virtual monopoly currently exists in the food industry and there’s a unhealthy link between Monsanto and the American government: Many people who have passed laws in the fields of food, drugs and agriculture were also, at some point on the payroll of Monsanto. In other words, the elite decides which foods are sold to you.

Public officials formerly employed by Monsanto:

  • Justice Clarence Thomas worked as an attorney for Monsanto in the 1970s. Thomas wrote the majority opinion in the 2001 Supreme Court decision J. E. M. Ag Supply, Inc. v. Pioneer Hi-Bred International, Inc.|J. E. M. AG SUPPLY, INC. V. PIONEER HI-BREDINTERNATIONAL, INC. which found that “newly developed plant breeds are patentable under the general utility patent laws of the United States.” This case benefited all companies which profit from genetically modified crops, of which Monsanto is one of the largest.
  • Michael R. Taylor was an assistant to the Food and Drug Administration (FDA) commissioner before he left to work for a law firm on gaining FDA approval of Monsanto’s artificial growth hormone in the 1980s. Taylor then became deputy commissioner of the FDA from 1991 to 1994. Taylor was later re-appointed to the FDA in August 2009 by President Barack Obama.
  • Dr. Michael A. Friedman was a deputy commissioner of the FDA before he was hired as a senior vice president of Monsanto.
  • Linda J. Fisher was an assistant administrator at the United States Environmental Protection Agency‎ (EPA) before she was a vice president at Monsanto from 1995 – 2000. In 2001, Fisher became the deputy administrator of the EPA.
  • Former Secretary of Defense Donald Rumsfeld was chairman and chief executive officer of G. D. Searle & Co., which Monsanto purchased in 1985. Rumsfeld personally made at least $12 million USD from the transaction.

Many laws (approved by ex-Monsanto employees) have facilitated the introduction and the consumption of genetically engineered foods by the public.

“According to current statistics, 45% of corn and 85% of soybeans in the United States is genetically engineered (GE). Estimates of 70-75% of processed foods found at our local supermarkets are believed to contain GE ingredients.

Other GE foods are canola, papayas, radicchio, potatoes, rice, squash or zucchini, cantaloupe, sugar beets, flax, tomatoes, and oilseed rape. One non-food crop that is commonly GE is cotton. The GE hormone recombinant bovine growth hormone (rBGH or Prosilac) was one of the first GE products allowed to enter the nation’s food supply. The U.S. Food and Drug Administration (FDA) approved Monsanto’s rBGH in 1993.”
- Anna M. Salanti, Genetically Engineered Foods

Although it is yet impossible to determine the long-term effects of genetically engineered foods on the human body, some facts have already been established. GE foods contain less nutrients and, most importantly, they are “chemical-friendly”.

“One of the features of GE foods is their ability to withstand unlimited application of chemicals, including pesticides. Bromoxynil and glyphosate have been associated with developmental disorders in fetuses, tumors, carcinomas, and non-Hodgkin’s lymphoma. Studies indicate that Monsanto’s recombinant Bovine Growth Hormone (rBGH) causes treated cows to produce milk with an increased second hormone, IGF-1. This hormone is associated with human cancers. Recommendations by the Congressional watchdog agency, Government Accounting Office (GAO), recommended that rBGH not be approved. The European Union, Canada, and others have banned it. The UN has also refused to certify that using rBGH is safe.”
– Ibid

Genetic modifications engineered by Monsanto makes their products bigger and more aesthetically pleasing. Another, less discussed “improvement” is the plants’ ability to withstand nearly unlimited amounts of Roundupbrand pesticides. This encourages farmers to use that brand of pesticides which is produced by … Monsanto.


Studies on Roundup link the powerful pesticide and herbicide to many health problems such as:

  • Increased risks of the cancer non-Hodgkin’s lymphoma
  • Miscarriages
  • Attention Deficit Disorder (the real one)

Fluoride

Another source of harmful chemicals is found in the modern man’s water supplies and soft drinks.  As of 2002, the CDC statistics show that almost 60% of the U.S. population receives fluoridated water through the taps in their homes. The official reason for the presence of fluoride in our tap water? It prevents tooth decay. Ok … really? Is this mildly important benefit worth the consuming of great amounts of this substance by the population? Some studies even denied the dental benefits of fluorided water.

“Scientists now believe that the main protective action from fluoride does not come from ingesting the chemical, with the teeth absorbing it from inside the body, but from direct absorption through topical application to teeth. This means swallowing water is a far less effective way to fight cavities than brushing with fluoridated toothpaste.”
- Source

So why is fluoride still found in tap water? Here are some quick facts about fluoridation chemicals:

  • they were once used as pesticides
  • they are registered as “poisonous” under the 1972 Poisons Act, in the same group of toxins as arsenic, mercury and paraquat
  • fluoride is scientifically classed as more toxic than lead, but there is about 20 times more fluoride than lead in tap water

Toxicity of fluoride compared to other poisons

Many studies have been conducted on the effects of fluoride on the human body and some notable adverse effects have been noted: it changes bone structure and strength, impairs the immune system and it was linked to some cancers. Another alarming consequence of fluoridation is its effects on brain functions:

“In 1995, neurotoxicologist and former Director of toxicology at Forsyth Dental Center in Boston, Dr. Phyllis Mullenix published research showing that fluoride built up in the brains of animals when exposed to moderate levels. Damage to the brain occured and the behavior patterns of the animals was adversely effected. Offspring of pregnant animals receiving relatively low doses of fluoride showed permanent effects to the brain which were seen as hyperactivity (ADD-like symptoms). Young animals and adult animals given fluoride experienced the opposite effect — hypoactivity or sluggishness. The toxic effects of fluoride on the central nervous system was subsequently confirmed by previously-classified government research. Two new epidemiological studies which tend to confirm fluoride’s neurotoxic effects on the brain have shown that children exposed to higher levels of fluoride had lower IQs.”
- Source

A lesser known, but extremely important side effect of fluoride is the calcification of the pineal gland.

Up until the 1990s, no research had ever been conducted to determine the impact of fluoride on the pineal gland – a small gland located between the two hemispheres of the brain that regulates the production of the hormone melatonin. Melatonin is a hormone that helps regulate the onset of puberty and helps protect the body from cell damage caused by free radicals.

It is now known – thanks to the meticulous research of Dr. Jennifer Luke from the University of Surrey in England – that the pineal gland is the primary target of fluoride accumulation within the body.

The soft tissue of the adult pineal gland contains more fluoride than any other soft tissue in the body – a level of fluoride (~300 ppm) capable of inhibiting enzymes.

The pineal gland also contains hard tissue (hyroxyapatite crystals), and this hard tissue accumulates more fluoride (up to 21,000 ppm) than any other hard tissue in the body (e.g. teeth and bone).

- Source

Other than regulating vital hormones, the pineal gland is known to serve an esoteric function. It is known by mystic groups as the “third eye” and has been considered by many cultures to be part of the brain responsible for spiritual enlightenment and the “link to the divine”. Is enlightenment out of bounds for the modern man?

“In the human brain there is a tiny gland called the pineal body, which is the sacred eye of the ancients, and corresponds to the third eye of the Cyclops. Little is known concerning the function of the pineal body, which Descartes suggested (more wisely than he knew) might be the abode of the spirit of man.”
– Manly P. Hall, The Secret Teachings of All Ages

Aspartame

Aspartame is an artificial sweetner used in “sugar-free” products such as diet sodas and chewing gum. Since its discovery in 1965, Aspartame caused great controversy regarding its health risks – primarily causing brain tumors – and was denied its application to be sold to the public by the FDA. Searle, the company attempting to market Aspartame then appointed Donald Rumsfeld as CEO in 1977 … and things changed drastically. In a short period of time, Aspartame could be found in over 5,000 products.

“Donald Rumsfeld was on President Reagan’s transition team and the day after he took office he appointed an FDA Commissioner who would approve aspartame. The FDA set up a Board of Inquiry of the best scientists they had to offer who said aspartame is not safe and causes brain tumors, and the petition for approval is hereby revoked. The new FDA Commissioner, Arthur Hull Hayes, over-ruled that Board of Inquiry and then went to work for the PR Agency of the manufacturer, Burson-Marstellar, rumored at $1000.00 a day, and has refused to talk to the press ever since.”
- Source

Years after its approval by the FDA, leading scientists still urge the organization to ban this product.

“Dr. John Olney, who founded the field of neuoscience called excitotoxicity, attempted to stop the approval of aspartame with Attorney James Turner back in 1996. The FDA’s own toxicologist, Dr. Adrian Gross told Congress that without a shadow of a doubt, aspartame can cause brain tumors and brain cancer and violated the Delaney Amendment which forbids putting anything in food that is known to cause Cancer. Detailed information on this can be found in the Bressler Report (FDA report on Searle).”
- Ibid

In 1995, the FDA was forced to release, under the Freedom of Information act, a list of ninety-two symptoms caused by aspartame reported by thousands of victims:

Those symptoms are however only the tip of the iceberg. Aspartame has been linked to severe illnesses and long term health issues.

“According to the top doctors and researchers on this issue, aspartame causes headache, memory loss, seizures, vision loss, coma and cancer. It worsens or mimics the symptoms of such diseases and conditions as fibromyalgia, MS, lupus, ADD, diabetes, Alzheimer’s, chronic fatigue and depression. Further dangers highlighted is that aspartame liberates free methyl alcohol. The resulting chronic methanol poisoning affects the dopamine system of the brain causing addiction. Methanol, or wood alcohol, constitutes one third of the aspartame molecule and is classified as a severe metabolic poison and narcotic.”
- Ibid

In Conclusion

If the main message of this website has been to this point “watch what enters your mind”, the main message of this article is “watch what enters your body.” The consumption of the products stated above will probably not cause an immediate and noticeable effect. But, after many years of ingesting those substances, one’s thoughts become increasingly clouded and foggy, the ability to concentrate becomes hindered and judgment becomes impaired. In other words, the once sharp mind becomes dull. What happens when a population is heavily sedated and poisoned on a daily basis? It becomes numb, zombie-like and docile. Instead of asking important questions and seeking a higher truth, the dumbed-down mass simply accomplishes its daily tasks and absorbs whatever the media tells them.  Is this what the elite is looking to create?

There is, however, a silver lining here. Many of the negative effects of the substances described above are reversible. And YOU are the one who decides what enters your body. This article provides a brief overview of dangers lurking for the unaware consumer, but tons of information is available on which to base enlightened decisions. Your body is a temple. Will you allow it to be desecrated?

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Tuesday, August 17, 2010

University of Georgia report reveals 80% of Oil from BP spill remains in Gulf… Why Are We No Longer Hearing From the Gulf?

Why are we not asking… insisting that media be allowed to report about the Gulf… without restrictions?  Why are your Congressmen and Senators not heading down there and reporting?  Why are the people from the Gulf not speaking up??  Where is the independent media??  Why are we sitting here and allowing ourselves to be led to the slaughter?

University of Georgia report reveals 80% of oil from BP spill remains in Gulf

(AXcess News) Atlanta - The University of Georgia says their latest study suggests up to 80% of the oil spilled in the Gulf of Mexico from the BP oil rig collapse is still present and remains a threat to the ecosystem.
The report was announced Monday, the same day the fall shrimping season began in the Gulf of Mexico.

The report, authored by five prominent marine scientists, strongly contradicts media reports that suggest that only 25 percent of the oil from the Deepwater Horizon oil spill remains.

"One major misconception is that oil that has dissolved into water is gone and, therefore, harmless," said Charles Hopkinson, director of Georgia Sea Grant and professor of marine sciences in the University of Georgia Franklin College of Arts and Sciences. "The oil is still out there, and it will likely take years to completely degrade. We are still far from a complete understanding of what its impacts are."

The group analyzed data from the Aug. 2 National Incident Command Report, which calculated an “oil budget” that was widely interpreted to suggest that only 25 percent of the oil from the spill remained.
Hopkinson notes that the reports arrive at different conclusions largely because the Sea Grant and UGA scientists estimate that the vast majority of the oil classified as dispersed, dissolved or residual is still present, whereas the NIC report has been interpreted to suggest that only the "residual" form of oil is still present.
Hopkinson said that his group also estimated how much of the oil could have evaporated, degraded or weathered as of the date of the report. Using a range of reasonable evaporation and degradation estimates, the group calculated that 70-79 percent of oil spilled into the Gulf still remains. The group showed that it was impossible for all the dissolved oil to have evaporated because only oil at the surface of the ocean can evaporate into the atmosphere and large plumes of oil are trapped in deep water.

Another difference is that the NIC report estimates that 4.9 million barrels of oil were released from the wellhead, while the Sea Grant report uses a figure of 4.1 million barrels since .8 million barrels were piped directly from the well to surface ships and, therefore, never entered Gulf waters.

On a positive note, the group noted that natural processes continue to transform, dilute, degrade and evaporate the oil. They add that circular current known as the Franklin Eddy is preventing the Loop Current from bringing oil-contaminated water from the Gulf to the Atlantic, which bodes well for the East Coast.
Joye said that both the NIC report and the Sea Grant report are best estimates and emphasizes the need for a sustained and coordinated research effort to better understand the impacts of what has become the world's worst maritime oil spill. She warned that neither report accounted for hydrocarbon gasses such as methane in their oil budgets.

"That's a gaping hole," Joye said, "because hydrocarbon gasses are a huge portion of what was ejected from the well."

Source: uga.edu  /  UGA News Service

FOR IMMEDIATE RELEASE
MEDIA CONTACT:
S. Smith (504) 593-9600
C. Brylski/H. Harper (504) 897-6110 begin_of_the_skype_highlighting  (504) 897-6110      end_of_the_skype_highlighting
August 16, 2010
News from Stuart Smith, Attorney Smith Stag LLC



Independent toxicologists issue warning:


We object to the FDA Claim that chemical dispersants have a low potential for accumulating in seafood and do not pose a public health concern Attorney Stuart H. Smith, representing the United Commercial Fishermen’s Association, the Louisiana Environmental Action Network, public and private entities, and citizens harmed by the BP oil catastrophe, today issued this statement:


“Independent analysis by toxicologists dispute FDA claims made in the last few days that chemical dispersants used by BP during the oil catastrophe may not accumulate in seafood.

“In fact, in a full report by Dr. Bill Sawyer released today, there is a grave problem caused by dispersants, due to the fact that these were used in deep waters and on such a vast scale.

“Studies of other spills show that the toxic components of crude oil ‘bio-accumulate’ into the food chain and become highly toxic to marine reproduction and harmful when consumed by humans, even when dispersants are applied at the surface and the chemical toxins may be sufficiently diluted over time to pose only minimal risks.

“However, BP’s use of dispersants deep underwater in the Gulf, and on such a vast scale, represents the first time dispersants have been used in this manner. The greatly-reduced biodegradation in the DEEPWATER HORIZON case, resulting from lack of sunlight, extreme cold temperatures at 5000 feet, and other environmental factors significantly reduce the rate at which the dispersed crude components are degraded.
“Eight months would be required to remove 96 percent of the petroleum under ideal conditions, thus we can only assume what remains in the Gulf waters will be a ‘toxic soup’ of chemicals for the foreseeable future, due to the worst-case scenario which has unfolded.

“The most potentially dangerous of the components in the Gulf’s toxic soup are ‘polynuclear aromatic hydrocarbons’ (PAHs), dangerous cancer-causing chemicals which slowly break down after being ingested by marine life, persist in marine organisms and can be passed to both humans and other wildlife through consumption.

“PAHs are not contained within the dispersants used, but rather, have been extracted from the BP crude and suspended in the water column via dispersant use.

“It must also be noted that the deep water National Oceanic and Atmospheric Administration Weatherbird analyses and our own near shore water, tunicate and beach samples have revealed a consistent pattern of dispersant-induced C19-C36 hydrocarbons and PAHs. Unfortunately, these specific PAHs are of the most toxic variety. Clearly, analyses of seafood in impacted regions require additional testing for PAH uptake protective of human carcinogenic potential.

“It is important that the public be vigilant and educate itself to these risks, as further compounding this misinformation from FDA are published news reports which show the government trying to discount university studies about the toxicity of the Gulf water column and seafood, and denying the continued use of dispersant spraying off the coast of Florida.”

FOR MORE INFORMATION: www.smithstag.com or www.oilspillaction.com

COMMENT:
  1. Don says:
I cannot imagine many worse case scenario’s than this described above. I must again ask this question. Where is the criminal investigations by the states ordered by the Governors into the actions of both federal authorities and BP? I don’t even want to hear that states can’t prosecute federal empolyees under some federal exemption clause because no person, no comapany, no government official is above the law when it comes to deliberate criminal actions such as using these dispersants which I know was hotly contested early on.
It is dereliction of their sworn duty for these state officials not to seek criminal and civil penalties against all those who had a hand in making the decision to use this dispersant at all and or gave cover for its use let alone in the massive qunatities that they did.
It’s time for some real action called guts in office not words. I certainly would not allow this to go on in Pennsylvania as its Governor and there would certainly be a very huge standoff over who trumps who when it comes to state sovereignty. I’d use what ever means were at my disposal as Governor as outlined in our Commonwealths Constitution and I mean everything and our Pennsylvania Constitution makes it clear what powers I have and who I can call up.

Monday, March 1, 2010

McCain’s Dietary Supplement Bill: An Attempt to Implement Codex Alimentarius

A bill recently introduced to the U.S. Senate, the Dietary Supplement Safety Act of 2010 (S. 3002), by Senators John McCain and Byron Dorgan is possibly the most direct assault on natural health freedom we have seen for some time. If passed into law, this bill would require all dietary supplement manufacturers, distributors, and holders all the way down to the retail store level to be comprehensively registered. It would also allow for the arbitrary banning of nutritional supplements by the FDA and the introduction of deceitful reporting of adverse events related to them.

supplements
The legislation effectively gives the FDA carte blanche to do whatever it wishes in regards to natural supplements.

The cover for this legislation is that it is designed to prevent both intentional and unintentional steroid adulteration of dietary supplements. The trigger, according to McCain, was six NFL players who were accused of doping with supplements tainted with steroids. Even with this being the case, however, the FDA already has the authority to regulate synthetic anabolic steroids via the Anabolic Control Act of 2004 which permits them to do just that. Nevertheless, under the guise of the behavior of six NFL players, an entire market that has been proven not only very safe but very healthy will be essentially regulated out of business. (NHF)

The Dietary Supplement Safety Act of 2010 would require registration of any “business or operation engaged in manufacturing, packaging, holding, distributing, labeling, or licensing a dietary supplement for consumption in the United States,” definitions which could possibly include even retail stores that sell herbal and nutritional products. (DSSA p.2) Currently, under the Dietary Supplements and Non-Prescription Consumer Protection Act, small retailers are not required to register. This, however, will change with the passage of McCain-Dorgan’s bill. (NHF)

The switch from the current practices of Serious Adverse Event Reporting to that of simply Adverse Event Reporting is of concern as well. Existing law requires the reporting of serious adverse events related to the supplement in question to be reported for regulatory and recall purposes. The McCain-Dorgan bill, however, removes the language “Serious Adverse Event” and replaces it with the term “adverse event,” opening up the floodgates for the most ridiculous possible claims of adverse events such as bad taste or even dislike of packaging. This “report everything possible” stance is will vastly increase the numbers of complaints that will hence be used to add credence to the arguments for banning supplements in the future. Not only that, but more government bureaucracies will have to be created in order to organize and sort through all of the incoming “adverse event reports.” (NHF)

Yet the most frightening aspect of this bill is the immediate effects it would have on natural supplements.

Currently, due to the Dietary Supplements Health and Education Act of 1994 (DSHEA), all supplements on the market prior to October 15, 1994 can lawfully be sold in the United States. However, the legislation being proposed completely reverses this and defines a “new dietary supplement” as one that “is not included on the list of ‘Accepted Dietary Ingredients’, to be prepared, published, and maintained by the Secretary” (DSSA p.5-6). This seemingly slight change in language actually removes the grandfathering in of supplements on the market prior to 1994. These new dietary supplements will also be considered “adulterated” unless “there is a history of use or other evidence of safety establishing that the dietary ingredient when used under the conditions recommended or suggested in the labeling of the dietary supplement….” (DSSA p.5) The registrants are then required to create and maintain a “scientifically reasonable substantiation file” which is to be made available for the Secretary of Health and Human Services to inspect at his/her whim. These products are to be registered at least 75 days prior to market. (NSF)

As quoted above, the bill also mandates that an “Accepted Dietary Ingredients” list should be created by the Secretary of HHS which will replace the current guidelines. Such a list effectively gives the FDA carte blanche to do whatever it wishes in regards to natural supplements. The FDA is given absolute authority to determine what supplements are allowed on the “Accepted Dietary Ingredients” list, thereby granting it the authority to ban any supplement without due process, scientific merit, or even a hearing simply by refusing to place it on the ADI list. (NSF) The FDA will also be able to remove supplements from market even after it has allowed it to be included on its’ list. As the bill states, “If the Secretary finds there is a reasonable probability that a dietary supplement or a product marketed or sold as a dietary supplement would cause serious, adverse, health consequences or death, or is adulterated or misbranded, the Secretary shall issue a cease distribution and notification order requiring the person named in the order to immediately – cease distribution of such dietary supplement or a product marketed or sold as a dietary supplement; notify distributors, importers, retailers, and consumers of the order; and instruct those distributors, importers, retailers, and consumers to cease distributing, importing, selling, and using the dietary supplement.”(DSSA p.9)

The cost of the recall, of course, will be absorbed by the retailer. (DSSA p.11)

While the Dietary Supplement Safety Act of 2010 is an egregious attack on Americans’ freedom of choice, it is also a symptom of an even larger problem. The McCain-Dorgan bill is not just another silly attempt by corrupt politicians to demonstrate that they still have some value to their constituents, but an attempt to implement Codex Alimentarius at the national level and move the United States away from our Common Law heritage. The European Union has already passed similar legislation in the European Union Food Supplements Directive which has decimated open access to natural dietary supplements. Canada has passed laws to the same effect in recent weeks as well.

Brandon Turbeville
Infowars.com - February 24, 2010

Works Cited:
“Dietary Supplement Safety Act of 2010.” February 2, 2010. http://mccain.senate.gov/public/index.cfm?FuseAction=Files.View&FileStore_id=2fe2fa5d-636b-4705-97df-8318a24f718f
“Bullet Points on McCain’s Anti-Supplement Bill S.3002.” National Health Federation. http://www.thenhf.com/press_releases/pr_19_feb_2010.html
“McCain Anti-DSHEA Bill a Clear and Present Threat to Health Freedom.” http://www.healthfreedomusa.org/?p=4608

Codex Alimentarius

Having spent the past twelve months investigating Codex Alimentarius, I am deeply disturbed by the almost total lack of awareness (or even interest) with regard to the implications of this pernicious global Commission, particularly amongst those most affected by the excesses of this restrictive legislation. In the words of the National Health Federation[i], the aims and objectives of Codex Alimentarius are as follows: * Only low-potency, “me too” supplements available that will do nothing for your health. * All or most foods genetically-modified. * Beneficial supplements unavailable or sold by prescription only. For many people, this agenda is so outrageous, they cannot believe such goals are achievable; yet this may well be the reality as soon as 31st December 2009, if the Codex Alimentarius Commission continues to disregard input from those who offer a counter perspective to the combined forces of Big Farmer & Big Pharma.

And yes, this is for real…

Does anyone ever wonder why American medicine is so anti-holistic practices??  Think Rockefeller and progressives~



The Mark Of The New World Order – RFID Chips are part of the provisions already passed in the Stimulus Bill that will kick in if ObamaCare passes.

New World Order at a Glance - Updated

Slavery of Freedom

Wednesday, July 8, 2009

Stop New Bill (HR2749) Gives FDA Unheard-of Power over Small Farmers, Food and Supplement Producers

A new, long-awaited food safety bill is now before the US House of Representatives. It is the Food Safety Enhancement Act of 2009, or FSEA. Introduced by Reps. Henry Waxman (D–CA) and John Dingell (D–MI), the FSEA is meant to address food safety concerns. But as you will see, much of it is not about food safety at all. Food safety issues have arisen from large agricultural operations. But this bill places its harshest burdens on small food producers and supplement producers.

Take Action and let your Representative know you DO NOT support this bill

The Food Safety Enhancement Act:

  • gives the US Food and Drug Administration (FDA) unprecedented scope, authority, and power over small farmers, food producers, and supplement producers, including the power to use vague language to intimidate and threaten;
  • imposes unjustifiably harsh criminal and civil penalties for even administrative violations; and
  • places undue economic hardship on small and mid-sized farms and food facilities (both organic and conventional), which could easily drive many of them out of business, and lead to monopoly control of food by large corporations.

Also known as the Waxman–Dingell bill, the Food Safety Enhancement Act has a number of provisions that would directly affect many of AAHF’s members. Although much of the bill’s language is vague—and, some worry, deliberately deceptive—it is clear that the FSEA provides for the following:

Sharply increased criminal and civil penalties for violations of FDA regulations.
The penalties include prison terms of up to ten years (jail time is currently capped at three years), and fines of up to $100,000 for individuals and $7.5 million for corporations, regardless of their size. The kicker is that these penalties are potentially applicable no matter what way you violate the FDA’s rules.

The application of those penalties to any food, drug, device, or cosmetic that is knowingly "adulterated or misbranded."

To our ears, “adulterated” means that it doesn’t meet good manufacturing practices, that the food itself is somehow tainted or injurious to health, or contains an ingredient that presents a significant or unreasonable risk of illness. And “misbranded” suggests deliberate misstatements about the efficacy of a product.
In FDA-speak, however, these words take on completely different meanings. For example, a food or supplement may be “adulterated” if some vague FDA rule is deemed by the FDA not to have been followed. “Misbranded” can mean that the producer makes a completely true statement about the product but without FDA permission. A cherry producer who cites peer-reviewed scientific research from prestigious universities on the health benefits of cherries would, in FDA-speak, have engaged in “false” and actionable “misbranding” which suddenly turns the cherries into drugs. Producers, of course, have the right to take cherries through the new drug approval process! In this and other ways, the FDA already censors science and quashes constitutionally protected free speech.

In this new bill, any violation of the new administrative requirements could make a product adulterated and/or misbranded. That is, an administrative violation (such as not keeping records exactly as required) that harms no one carries exactly the same penalty as a violation in which a product is adulterated during the manufacturing process and poses a significant risk of illness or ends up killing people.

The dramatic increase in jail time and fines will make supplement production an even riskier proposition than it is today. Supplement producers have to put some information on the bottle. They try their best to satisfy FDA rules, which can only be described as gray, not black and white. Now if they get it wrong in the eyes of the FDA, the potential penalties will be extremely severe.

Many on Capitol Hill are under the impression that the bill pertains only to food, but the FSEA language specifically names supplements as well, and this will have a huge potential impact on any small company brave enough to continue their manufacture and sale.

Large companies will probably be unaffected because they can afford the extensive legal staff needed. Moreover, the FDA does not try to put large companies with political clout out of business, much less put their executives in jail. General Mills (the manufacturer of Cheerios) was recently cited by the FDA for an unapproved health claim, even though the company was reporting good science. Under the new bill, General Mills could be fined $7.5 million, but based on past FDA performance this would be unlikely. If a tiny company were cited, the exact same fine would be applicable and the likelihood of being exacted would be much greater.

FDA control of farming standards and practices
Many people on Capitol Hill seem to believe that farms are exempted from the FSEA’s scope. That is false. On the contrary: the bill would empower the FDA to regulate how crops are raised and harvested. It puts the FDA, which knows nothing about farming, right on the farm, dictating to our farmers. Specifically, it allows the FDA to set “scientific and risk-based standards” for the use of fertilizers, harvesting and processing methods, transportation, etc. Any non-compliance means the food is to be considered “adulterated” (with fines of up to $100,000 per individual and $7.5 million per corporation, and a jail term of up to ten years).

For example, based on both its public statements and its record, the FDA is vehemently opposed to the consumption of raw milk (even in cheese) and would like to ban its distribution. If HR2749 becomes law, the agency would have much greater scope to go after raw milk than it did before, particularly targeting raw milk producers whose products cross state lines.

Raw milk is just one example. The FDA can decide that it doesn’t like anything under this bill. And we can be sure that large producers will have easy access to the agency to explain why competing products from small producers should be banned.

Moreover, the bill would give the FDA the power to order a quarantine of a geographic area. Under this provision, farmers markets and local food sources could be shut down, even if they are not the source of the contamination. The agency could halt all movement of all food in that geographic area.

The language is incredibly vague and does not distinguish between industrial-sized operations, organic farms, or smaller operations—the FDA could easily use its new authority to set requirements that only large corporate farmers can meet. While farms are exempt from some sections of the FSEA legislation, they are explicitly included in this all-important section. Smaller farmers who can’t meet the new FDA requirements will simply go out of business, unfairly creating monopolies for the huge corporations. We believe the FDA should not have this kind of authority over farms at all, but this one-size-fits-all approach has significant economic implications and could destroy a sustainable farm trying to comply with an inappropriate commercial standard.

An unequal burden for smaller and local food facilities
A food facility—defined as any factory, warehouse, or establishment that manufactures, processes, packs, or holds food—must, under the new bill, register and pay an annual registration fee of $500 (and that fee would be adjusted upward with inflation). Although farms and restaurants are exempt, the agency has defined “farm” narrowly, and people making small batches of foods such as lacto-fermented vegetables, cheeses, or breads would be required to register and pay the fee, which could drive start-up and small producers out of business during difficult economic times. A flat fee that does not take into account the size of the facility is good news for giant agribusinesses, but may represent a serious economic burden for some smaller companies struggling to make ends meet. How could the FDA think that the same fee (and penalties) are as appropriate for Mom-and-Pop operations as for ConAgra?

Moreover, FSEA provides for mandated electronic registration, which may be an issue for smaller producers, and is certainly a problem for Amish farmers, for whom the electronic filing requirement violates their religious beliefs. Failing to register a food facility would constitute “misbranding”; violators—you guessed it—would be subject to fines of up to $100,000 if the business is individually owned, $7.5 million if corporately owned, and/or ten years in jail.
Warrantless searches by the FDA

Under the bill, the FDA will have full authority to conduct random, warrantless searches of all records dealing with any aspect of a company’s production, manufacture, or distribution process. Under current law, the FDA only has access to records if it has “a reasonable belief that an article of food is adulterated” and presents “a threat of serious adverse health consequences or death to humans or animals.” Under the FSEA, however, the FDA has access to all records, at any time, and without any evidence whatsoever that there has been a violation. Warrantless searches are a powerful weapon of intimidation and harassment.

The bill also extends FDA’s authority to access records of a farm and restaurant—both of which are exempt from FDA’s reach under current law. Even farmers selling direct to consumers would have to provide the federal government with records on where they buy supplies, how they raise their crops, and a list of their customers.

The FSEA also gives the FDA complete control over recalls, seizures, detentions and quarantines—with no judicial oversight. For example, FSEA lowers the standard FDA must meet in order to conduct an administrative detention. Currently they must demonstrate “credible evidence” that a food presents a health threat before an administrative detention is allowed; the FSEA standard is “any reason to believe that an article of food is adulterated, misbranded, or otherwise in violation of this Act.”

Burdensome administrative requirements, including a new food tracing system
The FSEA requires all facilities, farms, and restaurants to implement new hazard analysis and risk-based preventive controls, food safety plans, and an extensive record maintenance program—again, without taking into account the differences between small facilities and large commercial facilities.

The FSEA also mandates an extensive food tracing system for all farms, or facilities that produce, process, or transport food, even if the food does not cross state lines, though at least “direct sales by farms” (i.e., sales directly to stores, restaurants, or consumers) are exempt—which means that most vendors who participate in a farmer’s market would not be affected. Each person in the production, manufacturing, processing, packing, transportation, or storage chain must “maintain the full pedigree of the origin and previous distribution history of the food” and must “establish and maintain a system for tracing the food that is interoperable with the systems established and maintained by other such persons.”

The bill does not explain how far the traceback will extend or how it will be done for multi-ingredient foods. With all these ambiguities, it's far from clear how much it will cost either the farmers or the taxpayers. Small farms may find this trackback system costly and time-consuming.

If the FSEA passes, only big businesses and large corporate farms will matter
With FDA having such vast control, authority, and access, globalization and harmonization of food quality is a step closer. HR2749 does not make any allowances for small- to mid-sized farms or facilities, which could mean economic ruin, closure, or dependence on large corporations or foreign food supply sources.

Let’s say you’re a small organic farmer, and you have a roadside stand on your own property. If this bill passes, you would now have to follow federally established standards for growing your produce, or your food would be considered adulterated. You could not, of course, say anything about the scientific basis for organic produce being healthier than conventionally farmed produce.

Further, you would be required to make your business records available to FDA inspectors. The inspectors would have the power to show up unannounced without a warrant to search your records without any evidence whatsoever that you have committed a violation of the law. If you refuse to let the inspector see your records, you would be guilty of adulteration.

If you’re a farmer who sells products direct to consumers, you would be forced to give the FDA any customer information you have in your records. No more customer privacy. Should you refuse, you’d face up to ten years’ imprisonment. The civil fines could be up to $100,000 if you’re an individual or $7.5 million if you incorporated your family farm as a business.

There is one bright note in a rider to the bill: HR2749 at least imposes a deadline on the Secretary of Health and Human Services to notify Congress by December 31, 2009, of the final determination on the safety of BPA (Bisphenol A) in food and beverage containers.

Please take action immediately!

We need every concerned American to contact his or her congressional representatives immediately and ask that HR2749 be defeated or, at the very least, amended.

Click here to be taken to our Action Alert and contact your Representative!

1-202-224-3121 – House Switchboard

1-202-225-3121 – House Switchboard

(202) 225-0100 - Speaker of the House Pelosi


Speaker Nancy Pelosi
http://speaker.house.gov/contact or http://www.speaker.gov/contact

If the web contact form doesn't work, use this email address:
AmericanVoices@mail.house.gov

Source: True Health Is True Wealth /American Association for Health

"Control oil and you control nations; control food and you control the people." …Henry Kissenger

Related Resources:

Posted: Knowledge Creates Power

Wednesday, June 10, 2009

Big Pharma and the FDA: Suppress the Science, Ban the Natural Substances, Sell the Drugs!


In 2005, an up-and-coming pharmaceutical company made a big mistake: they invested millions of dollars into developing a drug only to discover that the only active ingredient of the drug, pyridoxamine, was really a common, naturally occurring substance that has been sold for decades at low cost to consumers in the form of a dietary supplement, and has always been available in commonly consumed foods such as chicken and brewer’s yeast.

We’re taught as children that when you make a mistake, you should own up to it and face the consequences. Apparently the pharmaceutical company in question, Biostratum, Inc., has yet to learn that lesson. Instead of owning up to their mistake, Biostratum tried to game the system to their advantage by asking the US Food and Drug Administration (FDA) to declare supplements containing pyridoxamine “adulterated” and effectively ban anyone but Biostratum from selling pyridoxamine.
Sadly, Biostratum’s desparate ploy to save their investment worked. Earlier this year the FDA agreed to ban companies from selling pyridoxamine as a dietary supplement. They denied the request to declare products containing pyridoxamine “adulterated,” but instead they declared that such products are not dietary supplements at all—claiming they are excluded from the definition of dietary supplements under the “prior market clause” [21 U.S.C. 321(ff)(3)(B)(ii)] and so may not be marketed as such.

Please note that nowhere in the FDA’s response letter is anything said about safety concerns. In fact, the FDA’s letter specifically says that “to allow such an article to be marketed as a dietary supplement would not be fair to the pharmaceutical company that brought, or intends to bring, the drug to market.” Fair to the pharmaceutical companies? What about fairness to consumers, some of whom rely on affordable pyridozxamine supplements to provide the levels of vitamin B-6 required for their survival? Is it fair to force those consumers to pay for expensive prescription drugs and doctors’ visits to supply their B-6 needs when they could get the exact same thing for a fraction of the cost in the form of a supplement? Isn’t this why our health care system is so ineffective?

This is hardly the first time the FDA has attacked naturally occuring substances. On October 17, 2005, the FDA banned information about the health benefits of cherries from appearing on websites—scientifically proven benefits, such as tart cherries’ ability to reduce the risk of colon cancer because of the anthocyanins and cyanidin contained in the cherry. Cherries, according to the latest research, help ease the pain of arthritis and gout; reduce risk factors for heart disease and diabetes; help regulate the body’s natural sleep patterns, aid with jet lag, prevent memory loss, and delay the aging process; and helps lower body fat and cholesterol—risk factors associated with heart disease. Moreoever, Scientists at Johns Hopkins have found that tart cherry anthocyanins reduced painful inflammation as well as a non-steroidal anti-inflammatory drug, indomethacin.

When the 2005 ban was instituted, the FDA sent warning letters to twenty-nine companies that market cherry products. In these letters, they ordered the companies to stop publicizing scientific data about cherries. According to the FDA, when cherry companies disseminate this peer-reviewed scientific information, the cherries become “unapproved new drugs” and are subject to seizure. The FDA warned that if those involved in “cherry trafficking” continue to inform consumers about these scientific studies, criminal prosecutions would ensue.

But fresh fruit and vegetables are not the FDA’s only target: As we reported in this newsletter recently, General Mills was recently issued a warning letter by the FDA for illegally marketing Cheerios Toasted Whole Grain Oat Cereal. The problem was the claim on the cereal box that Cheerios can lower cholesterol 4% in six weeks, and the statement on their website that “diets rich in whole grain foods can reduce the risk of heart disease.” The letter, dated May 5, 2009, called the above claims “serious violations” of the Federal Food, Drug, and Cosmetic Act and applicable regulations.

FDA stated that based on the claims made, Cheerios is now an unapproved drug, and must go through FDA new drug approval process.Note that the FDA isn't disputing the claim. It's disputing the company's right to make the claim.

As one newspaper columnist humorously put it, “One of these things is not like the others: morphine, penicillin, aspirin, Cheerios. Most drugs, if taken improperly, will kill the consumer or cause substantial bodily harm. An entire bottle of aspirin at one sitting will harm or kill. If Cheerios is a drug, therefore, one should be able to commit suicide by consuming the entire box.”

For years, the FDA barred health claims about the benefits of fish oil for heart, cancer, depression, body pain, and various other conditions until a drug company paid a great deal of money to go through the approval process. This type of enforcement effectively censors scientific information and greatly restricts consumer access to scientific studies that provide valuable information.

In the case of pyridoxamine, the FDA did not act out of concern for public safety. This is about money, and about a profit-seeking corporation taking advantage of what is supposed to be a public health organization in order to save their skins.

Source: American Association for Health Freedom

Related Articles:

Posted: True Health Is True Wealth

Friday, May 8, 2009

A Country Gone Crazy... Is $17 Bill in Budget Cuts a Lot or a Little?

Our World News report:

-- jpt - May 08, 2009 6:40 AM

Source:  ABC News/Glenn Beck

A Country Gone Crazy... An Administration Out of Control

  • $17 Billion in Budget Cuts Is Now, That The Debt And Budgets Have Doubled And Tripled, A Substantial Amount to Save, Says Obama. During The Campaign When McCain Said He Would Cut Earmarks by $18 Billion, Obama Said It Was a Drop In The Bucket.
  • With All The Violence at the Border, The Warning Of The Swine Flu Epidemic Possibilities, On-Going Terrorist Threats, And The Flo of Drugs And Guns Across The Border, Funds for Border Security Have Been Cut From Budget
    • Border Fence Not To Be Built Even Though Money Has Been Allotted???
  • Funds For Families Of Fallen Policemen Cut
  • Tax Cheat Tim Geithner Going to Head-up Task Force To Aggressively Collect Taxes
  • Peek At New Health Plan - People Will Pay Co-Pay For Their Employer Supplied Healthcare (An Employment Benefit) And Then "Taxed" on Their Benefits to Pay For Those Who Can't Afford Healthcare
  • Evidence, From Homeland Security, Shows That Nancy Pelosi Knew About EIT, But “They” Want To Prosecute People From The Last Administration Like A Banana Republic.  
  • Hmmm… What Happened To Obama’s Promise Of Tax Cuts And No New Taxes… Cap and Trade, Healthcare Coverage Tax, Higher Taxes On The Wealthy Who Create Jobs In The United States
  • Billions In Bailouts To Save The Car Companies And Now Chrysler Will Essentially Be An Italian Company After Filing For Bankruptcy… After Getting the Bailout Money and Today It Was Announce That GM Will Be Creating More Jobs And Making More Cars… In Mexico And China
  • Former Employees Of ACORN (Part Of The Board Of Directors) Are Coming Forward And Admitting To Voter Fraud and Internal Fraud.  Say ACORN Is Getting Federal And Bailout Money Through Sub-Companies.
  • Leaders of Freddie And Fannie Were At ACORN Offices During Their Bailout Period.
  • Security At Our Nation's Ports Is One Of the Proposed Budget Cuts.
  • Bloggers Are Being Threatened With Legislation For Jail Time To Silence Them.
  • Conservative TV and Radio Are Being Threatened And Targeted By The Powers That Be.
  • And The List Goes On… And On... And On
Everyone Needs To Wake Up, Pay Attention, Read... Even If You Are Not A Reader, Listen To A Spectrum and Variety of New Coverage, And Take Part In The Process.  We Need To Insist On The Transparency That We Were Promised During Obama's Campaign.

Doug Mills/The New York Times

President Obama, with Peter R. Orszag, the director of the Office of Management and Budget, and Rob Nabors, his deputy, unveiled nearly $17 billion in additional budget cuts for the coming fiscal year.


Published: May 7, 2009

WASHINGTON President Obama on Thursday unveiled nearly $17 billion in additional budget cuts for the coming fiscal year to underscore what he called an “ongoing” effort to find savings at a time when the government’s costs for bailouts, health care and wars are mounting far faster.

“We can no longer afford to spend as if deficits do not matter and waste is not our problem,” said Mr. Obama, who was joined at the White House by Peter R. Orszag, the director of the Office of Management and Budget, and Rob Nabors, his deputy. “We can no longer afford to leave the hard choices for the next budget, the next administration — or the next generation.”

The savings for the budget year starting Oct. 1 represent the sum of Mr. Obama’s promised “line by line” scrubbing of the federal budget, and the the proposed cuts amount to about 1.4 percent of the $1.2 trillion deficit that is projected for the fiscal year 2010.

Administration advisers called the cuts just a beginning, but some Republicans said they were less than impressed.

“While we appreciate the newfound attention to saving taxpayer dollars from this administration, we respectfully suggested that we should do far more," said Representative John A. Boehner of Ohio, the House Republican leader.

The president’s 10-year budget outline, released in February, shows the deficit declining by his final year in office to $533 billion, mostly through assumptions about economic growth when the recession ends and which many economists consider somewhat optimistic.

The $17 billion would be saved by ending or reducing 121 federal programs.

Mr. Obama listed some of them: a long-range radio navigation system that costs $35 million but has been rendered obsolete by global positioning systems; a literacy program that spends half its financing on overhead, and will be absorbed by other Education Department efforts; and the position of education attaché to UNESCO, based in the United States Embassy in Paris.

“Participation in UNESCO is very important,” Mr. Obama said, “but we can save this money and still participate using e-mail, teleconferencing, and a small travel budget.”

The the 131-page budget document released Thursday showed spending in 2008 of $77,000 to rent living quarters for the attaché, and $21,000 for travel expenses, and the president noted that eliminating the position would save $632,000 a year.

An additional $142 million would be saved by ending a program to clean up abandoned mines. But eliminating the financing illustrates the difficulties the administration could face in Congress, where, as administration officials acknowledged, every program has its patrons. When Mr. Obama proposed cuts in the program as part of his budget outline, Western state lawmakers objected.

“None of this will be easy,” he said.

That is certainly true for about half of the savings that administration officials say will come from military programs. The savings proposals, outlined last month by Defense Secretary Robert M. Gates as part of a comprehensive reordering of military spending priorities, drew howls of protest from supporters in Congress and the arms industry.

Among Mr. Gates’s targets are missile defense programs, the Armys costly Future Combat Systems, Navy shipbuilding, the advanced F-22 fighter jets and a state-of-the-art helicopter fleet for the president.

“This is a product of going through the budget line-by-line,” as Mr. Obama has promised since his presidential campaign, Rahm Emanuel, the White House chief of staff, said. “It’s a constant, cumulative effort on this front to find savings and find reductions.”

While the $17 billion in projected savings represents a small portion of the proposed budget, Mr. Obama insisted that “that’s a lot of money, even by Washington standards.” It was enough to pay for a $2,500 tuition tax credit for millions of students, for larger Pell education grants, he said, “with enough money left over to pay for everything we do to protect the National Parks.”

“For every dollar we seek to save there will be those who have an interest in seeing it spent,” the president said. “That’s how unnecessary programs survive year after year. That’s how budgets swell.”

But, he added, “We cannot accept business as usual.”

Brian Knowlton contributed reporting

There are objections and criticisms coming from "both sides of the aisle" on the proposed 2010 budget cuts. The White House released details of President Obama’s proposed budget for the 2010 fiscal year today. For anyone who would like to read it, the whole deal is online here; Here’s the proposed budget for Health and Human Services.

The WSJ is reporting that the budget includes a $300 million funding boost for the FDA, (this is not a good thing) the largest in the agency’s history.

"Time to take the 'red pill' so you can see past the Matrix, America!!"

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