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FDA’s Vicious Attack on Dietary Supplements

Posted on 14 September 2011 by admin

By Dr. Mercola

S.1310: Dietary Supplement Labeling Act of 2011, introduced at the end of June by U.S. Senator Richard Durbin (D-Illinois) is, using Byron J. Richards’ words, “an alarming regulatory nightmare that is trying to treat vitamins as if they are drugs.”

Its stated purpose is to:

“… improve the safety of dietary supplements by amending the Federal Food, Drug, and Cosmetic Act to require manufacturers of dietary supplements to register dietary supplement products with the Food and Drug Administration and to amend labeling requirements with respect to dietary supplements.”

As is typical of most diabolical laws, it initially sounds harmless enough. But there’s more. Durbin’s bill goes hand-in-hand with new FDA regulations that amend the definitions for new dietary ingredients (NDI’s), and together, they can threaten your health and freedom of choice, and further serve to strengthen the fatally flawed paradigm of health and medicine.

We’ve seen proposed legislation that sorely threatens your health and well-being before, but this time they’re really trying to hit the alternative health field, and your right to take control of your own life, hard.

It’s Not about Safety, It’s about Profits

Whose profit, you might ask?

Why, the pharmaceutical industry, of course. Vitamins, minerals and herbal supplements have a tremendously safe track record. Drugs are known to cause well over 100,000 deaths per yearwhen taken as prescribed.

For comparison, look at the latest statistics available from the U.S. National Poison Data System, which covers acute poisonings. In 2007, 1,597 people reportedly died from drugs. Meanwhile there was not one single fatality caused by a vitamin or dietary mineral supplement that year. Yet, Durbin and the FDA want you to think that they’re just acting in your best interest. Nothing could be further from the truth!

Up to this point, the FDA has had to prove a supplement unsafe in order to take action against it, but now they want the supplement industry to prove the safety of what in many cases amount to food, before they can reach the market.

Why add an extremely costly testing and approval process for compounds that are inherently safe? Well, an obvious side effect of these proposed regulations will be the elimination of small and medium sized companies, which in turn will drive up costs while at the same time reduce your access to historically safe nutritional products. The end result is that fewer people will use supplements to improve their health; driving them back into the extremely profitable fold of conventional medicine and drugs.

Byron J. Richards writes:

“The elimination of health options is required for the control of a population, while the preservation of health freedom is a leading indicator of the overall freedom within a society… [T]he control of health options is as important as the control of food and money.

… Big Pharma influences Republicans by aligning itself as a corporate conglomerate that is too big to fail, one that should be free of prudent safety regulations or reduction in grotesquely inflated prices. It fights against drug safety at every turn, while at the same time lobbying to pass laws that lock in sales or eliminate its competition.

The media plays along, as Big Pharma is a wonderful source of advertising dollars that are in no small part made possible by taxpayer funding of Big Pharma drug sales. While Big Pharma sees many aspects of the dietary supplement industry as competition, it is also the case that many pharmaceutical companies are in some aspect of the dietary supplement industry, often as raw material suppliers.

Big Pharma does not want to see the dietary supplement industry eliminated, it wants to see the small and medium sized independent businesses in the dietary supplement industry eliminated and it wants to own the industry. Their key strategy to accomplish this at this time is to lobby to pass costly laws and regulations which they can comply to and which other smaller, independent companies cannot. “

The Second Part of an Orchestrated Attack

Back in the early 1990s, the FDA threatened the availability of dietary supplements to the point that consumers staged a massive revolt, which resulted in the Dietary Supplement Health and Education Act of 1994 (DSHEA). The law specifically protects your access to dietary supplements by classifying them as foods, not food additives or drugs, and it grand-fathered in dietary supplements that were already in use as of 1994. Only novel ingredients introduced after October 15, 1994 are required to seek FDA approval.

Now, along with Durbin’s bill, the FDA has concocted new proposed mandates regarding the definition of a New Dietary Ingredient , known as NDI, that can be retroactively applied to products already on the market.

You can read the FDA Draft Guidance on New Dietary Ingredients (NDI’s) here. A detailed analysis of the FDA Draft Guidance is also available.

According to Richards:

“It is important to understand that this is a Durbin effort to ruin the dietary supplement industry, using both newly proposed legislation (S.1310) and retroactively redefining the DSHEA law through new FDA regulations to reflect what is being proposed in S.1310 – undermining the clear intent of the DSHEA law.

The DSHEA law intended consumers to have wide access to dietary supplements. Durbin is intent upon the opposite.” These regulations seek to change what was essentially a notification process into a costly approval process. The net effect of the regulations is to reclassify many nutritional compounds currently on the market as NDI.”

The DSHEA legislation states that:

  • the Federal Government should not take any actions to impose unreasonable regulatory barriers limiting or slowing the flow of safe products and accurate information to consumers;
  • dietary supplements are safe within a broad range of intake, and safety problems with the supplements are relatively rare;
  • and legislative action that protects the right of access of consumers to safe dietary supplements is necessary in order to promote wellness

The proposed mandates directly contradict what DSHEA sought to prevent, and the FDA is using its authority in direct violation of Congressional intent. As explained in an article by Alliance for Health, the proposed regulations turn what was clearly supposed to be a pre-market notification system into a pre-approval system, just like that of drugs. As a result, dietary supplements that have been freely available for nearly two decades can be forced off the market until they receive NDI approval. And the NDI approval process is a lengthy affair that may take months or years to complete, and cost a small fortune.

What might make an “old” ingredient “new,” under the new regulation?

The methods of production and extraction, for example… As bizarre as that sounds, the mere fact that a product is being extracted or produced by improved means compared to methods used in the past, could reclassify any grandfathered nutrient as an NDI that would now have to undergo the same type of safety testing and approval process as a drug.

Ridiculously Excessive Safety Testing Would be Required Under New Rules

If the FDA and Durbin get their way, once a supplement is taken off the market pending approval as an NDI, the manufacturer would have to conduct outrageously expensive studies using abnormally high doses—in some situations multiplied by a “safety factor” up to 2,000-times the recommended dosage on a per product basis. In fact, some of the safety thresholds are in excess of those required by pharmaceutical drugs despite studies showing supplements are FAR safer than drugs!

An estimated 106,000 hospitalized patients die each year from drugs that, by medical standards, are properly prescribed and administered, and two million more suffer serious side effects. How does the safety of supplements compare?

  • In 2001, 84.6 percent of all substances implicated in fatal poisonings were pharmaceutical drugs, according to that year’s American Association of Poison Control Centers (AAPCC) report. This compares with 0.8 percent for all dietary supplements combined, even including substances such as dinitrophenol, a dangerous (and illegal) substance banned in 1938, as well as the central nervous system stimulant Ma Huang (Ephedra).

    ONE drug alone, the anti-asthma drug theophylline, which was responsible for 15 deaths that year, amounted to 66 percent more than all the available dietary supplements combined.

  • According to CDC mortality data for 2005, prescription drugs killed more than 33,500 people that year, second only to car accidents. That same year, the American Association of Poison Control Centers reported 27 deaths that were associated with dietary supplements (one of which was reportedly due to Ephedra; the herbal supplement banned the year before for being too dangerous. In 2005, low-dose Ephedra was also subsequently banned).

Now, since dietary supplements are not patented drugs with outrageous profit margins, very few supplement makers will be able to afford the required safety studies, which could run in the millions of dollars per ingredient! Furthermore, the manufacturer is not the only one that would have to seek approval—every distributor that wants to use the NDI would have to file a separate NDI application.

Get Involved NOW!

Folks, this is not the time to doze off on the sidelines. Durbin’s bill and the FDA proposed mandates for NDI’s are a poorly veiled attempt to usurp your rights and health freedom. As Richards writes:

“This chess game is being played with a pathetic opening strategy based on imaginary safety problems. The gambit requires an ignorant public for its success.

It’s time to prove them wrong yet again, just like we did back in 1994. The open comment period on the FDA’s proposed guidelines expires on September 30, 2011. It’s vitally important for everyone to file a written protest and not allow them to rewrite the intent of the DSHEA law. Durbin’s bill and the FDA proposal pose a direct threat to your health and longevity, so please, step up and defend your right to continue using supplements and to gain access to new natural ingredients with demonstrated efficacy by following the steps outlined below:

  1. Write to your State Senators and tell them to beware of S.1310 and to vote NO on it.

  2. Log on to www.lef.org/lac to send a written petition to the FDA, or use the sample letter provided below. Print out this petition and add any words you choose and fax this to the FDA at the following number: (301) 443-9767
  3. Call FDA at 1-888-723-3366 and read this petition to personnel at the Office of Nutrition, Labeling and Dietary Supplements
  4. Send a Freedom of Information Act (FOIA) request by logging in to lef.org/FOIA to find out what pharmaceutical interests are behind these absurd proposals that will cause the cost of what supplements remain on the free market to skyrocket in price. (Sample letter is also provided below.)
  5. Send a letter to your Representative and two Senators demanding the FDA immediately withdraw their oppressive proposed guidelines pending rationale discussions with those who depend on dietary supplements to protect their health and livelihood. You can do this easily by logging into www.lef.org/lac, or use the sample letter below.

Empower yourself today. Recall how Consumers revolted back in 1994 and the result was a glorious victory over FDA tyranny!

Let your voice be heard by logging on to www.lef.org/lac today and exercising your right to petition the government against these serious violations of the law and scientific principle.

SAMPLE FDA PETITION:

PLEASE NOTE, it is best if you customize or change the letter below to state your specific concerns and beliefs as it will be better. If you are unable to then you can send the one below but it will work MUCH better if you can customize it.

TO: Center for Food Safety and Applied Nutrition

Office of Nutrition, Labeling and Dietary Supplements

Food and Drug Administration

5100 Paint Branch Pkwy.HFS-009

College Park, MD 20740-3835

Telephone:1-888-723-3366

Fax: (301) 443-9767

On July 11, 2011, President Obama issued an Executive Order that requires the FDA to:

  1. Make regulatory decisions only after consideration of their costs and benefits (both quantitative and qualitative).
  2. Review significant regulations to make sure they are not excessively burdensome.
  3. Develop and release to the public a plan within 120 days under which the FDA will periodically review its existing significant regulations to determine whether any such regulations should be modified, streamlined, expanded, or repealed so as to make the agency’s regulatory program more effective or less burdensome in achieving the regulatory objectives.

I am petitioning the FDA regarding your draft guidance on New Dietary Ingredient notifications for dietary supplements (known as Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues).

I demand that you immediately disregard all the proposals you outlined and instead consider a rationale and scientific approach to regulating new dietary ingredients that will be submitted to you by the Alliance for Natural Health within the next 180 days.

Your proposed guidelines on New Dietary Ingredients will cause the price of my supplements to skyrocket and some of these life-sustaining supplements are likely to disappear altogether.

This is not acceptable, especially when there are no significant reports of adverse reactions to the supplements you plan to ban.

In as much as your threat to ban my access to new dietary ingredients is causing me great anxiety which is injurious to my health, I insist that you immediately put your proposed new rules on hold for a 180 day period so that the Alliance for Natural Health can draft guidelines that will protect me against unsafe ingredients without destroying my access to low cost effective nutrients.

Sincerely,

Name___________Address____________City___________ST____ Zip___

SAMPLE LETTER TO CONGRESS:

The Honorable ______________________, Washington, DC

In direct violation of the law, the FDA is threatening to ban my access to new dietary supplements.

The FDA defines dietary supplements as being “new” if they were introduced after October 15, 1994. That means that nutrients that I have been safely using over the course of three decades will be subject to FDA’s oppressive policies that mandate costly animal testing, which translates into forced withdrawal from the market, and higher prices for me if the supplement is ever allowed to be sold again.

The Dietary Supplement Health and Education Act of 1994 states that:

The Federal Government should not take any actions to impose unreasonable regulatory barriers limiting or slowing the flow of safe products and accurate information to consumers.”

It says that Congress finds that:

dietary supplements are safe within a broad range of intake, and safety problems with the supplements are relatively rare.”

And it says that:

legislative action that protects the right of access of consumers to safe dietary supplements is necessary in order to promote wellness.”

This draft guidance does the exact opposite of what Congress intended. It imposes unreasonable barriers that limit and slow the flow of safe products and accurate information to consumers. I call upon Congress to:

  1. Uphold the landmark legislation it passed seventeen years ago, and to direct the FDA to revise its New Dietary Ingredient draft guidelines to reflect DSHEA’s (and Congress’s) stated values and goals.
  2. Vote against the newly introduced Dietary Supplement Labeling Act as this would give the FDA even greater arbitrary powers to remove safe dietary supplements from the market, which will a profoundly adverse impact on this nation’s health.

All of these proposals results in wasteful federal spending, while imposing a massive new “regulatory tax” on consumers and the vitamin industry.

Kindly let me know what actions you are taking in response to the urgent issues raised in this letter.

Sincerely,

Name______________Address____________City___________ST____ Zip___

SAMPLE FOIA REQUEST:

Below is a sample letter that you can use to select one or more of the 19 listed requests for records, or create your own individual request. You can then copy, edit, print, and send this to the FDA at the address on the letter. Please note that you are committing to paying a $25.00 charge if FDA agrees to respond to your request. The more records you request, the greater the FDA fees are likely to be. If you choose to file a Freedom of Information Act request, please read this letter carefully.

Date: _____________
Food and Drug Administration

Division of Freedom of Information

Office of Shared Services

Office of Public Information and Library Services

12420 Parklawn Drive

ELEM-1029

Rockville, MD 20857

Re: Freedom of Information Act Request

Dear FOIA staff:

Pursuant to the Freedom of Information Act, 5 U.S.C. §552, we wish to have copies at the earliest possible time, of any and all public records in the custody of the Food and Drug Administration that relate to the “Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues” released in July 2011.

I specifically request:

  1. All records relating to the expenditure of time and money by FDA personnel (and outside consultants) in researching, drafting and promulgating the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  2. All records relating to communication of FDA personnel with pharmaceutical company representatives (including lobbyists) that in any way relate to the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  3. All records relating to communication of FDA personnel with any member of Congress or Congress as a whole that in any way relate to the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  4. All records relating to communication of FDA personnel with any member of private industry that in any way relate to the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  5. All records relating to communication of FDA personnel with any scientific advisory committee, scientific advisory board, or individual scientist that in any way relate to the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  6. All records relating to communication of FDA personnel with FDA’ General Counsel’s office, or outside legal counsel that in any way relate to the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  7. All records relating to FDA’s evaluation of safety issues relating to new dietary ingredients that in any way relate to the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  8. All records relating to FDA’s decision to impose barriers that limit the ability of consumers to access new dietary ingredients that in any way relate to the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  9. All records relating to communication of FDA personnel with other FDA personal that in any way relate to the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  10. All records relating to communication of FDA personnel with personal from the Department of Health and Human Services that in any way relate to the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  11. All records relating to communication of FDA personnel with personal from the U.S. Treasury Department that in any way relate to the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  12. All records relating to the cost benefit analysis performed by FDA or outside consultants that in any way relate to the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  13. All records relating to financial estimates made by FDA personnel or outside consultants relating to the cost to the FDA of administering the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  14. All records relating to financial estimates made by FDA personnel or outside consultants relating to the cost burden of the dietary supplement industry in complying with the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  15. All records relating to what human and other resources within the FDA would be utilized to oversee and administer the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  16. All records relating to what human and other resources within the FDA would be moved or transferred from other positions within the FDA in order to oversee and administer the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  17. All records relating to communication of FDA personnel with the Department of Justice that in any way relate to the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  18. All records relating to the steps taken by the FDA to ensure the Administrative Procedures Act was fully complied with as it relates to the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.
  19. All records relating to the steps taken by the FDA to ensure that provisions in the Dietary Supplement Health and Education Act of 1994 was fully adhered to as it relates to the Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.

I agree to pay any and all expenses up to $25.00 related to this request. If you anticipate that the nature or volume of the records requested is such as to require extensive use of information technology, resources, or extensive clerical or supervisory assistance by personnel of the Food and Drug Administration, and such expenses would exceed $25.00, I would appreciate being advised thereof in advance of the assembly of those records and the estimated charge in excess of $25.00, if any, for doing so.

If the FDA asserts an exemption from Public Records Act disclosure of any records falling within the scope of the above request, we request that it include in the records inspected, or otherwise make available to us as soon as possible and in no event no later than the date of the initial production of the records, a reasonable description of the nature of the records for which an exemption or exemptions are claimed and the statutory or other legal bases under any such exemption is claimed.

I would appreciate your contacting me, at ___________ at the earliest possible time to advise us of when the FDA will make the requested copies available.

Please call if you have any questions regarding this request.

Sincerely,

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Obama Tells Farmer No Need to Worry About Over-Regulation of Agriculture

Posted on 18 August 2011 by admin

Obama Tells Farmer No Need to Worry About Government Over-Regulation of Agriculture

Thursday, August 18, 2011 – by Mike Adams

Mike Adams

(NaturalNews) During a town hall meeting yesterday, when an Illinois farmer told President Obama he was concerned about upcoming regulations regarding the Food Safety Modernization Act and would rather be farming than “filling out forms and permits,” Obama had choice words to offer in reply: “Don’t always believe what you hear.”

For once, Obama has told the truth. “Don’t always believe what you hear” should be the rally cry for all the farmers, raw dairy producers and consumers harmed by government actions taking place under the Obama administration – actions which can only be called war against the People and crimes against nature.

It was Obama’s USDA, for example, that approved genetically modified alfalfa to be openly planted everywhere, thereby contaminating non-GMO alfalfa crops with DNA pollution that’s impossible to remove from the harvest. This is the same USDA that also recently said it would do nothing to halt the release of GMO yard grass seeds into the marketplace.

Because of that decision, by the Spring of 2012, we could see genetically engineered lawns spouting up in neighborhoods all across America, where they will be frequently sprayed with toxic Roundup herbicide chemicals.

It was under President Obama that the FDA masterminded the recent armed raids on American raw dairy farmers by bringing a SWAT team to an L.A. food distribution center. There, under the watchful eye of federal government thugs, agents proceeded to pour all the milk down the drain, then seize and destroy tens of thousands of dollars worth of cheese, watermelons, mangos and other valuable food.

Obama, of course, could have stopped this outrageous incarceration of raw dairy farmers at any time but he stood back and said nothing. Perhaps he was too busy going on vacation to take any meaningful action to try to protect American farmers from gun-toting government tyrants.

It was under Obama’s watch that Michigan gardener Julie Bass was threatened with 93 days of jail time for growing tomatoes in her own front yard. While this wasn’t a federal case (it was drummed up by local tyrants who run the city of Oak Park), Obama could have easily intervened with a national message about “the freedom to garden.”

Where was Michelle Obama on this point in particular? The president’s wife can grow a garden on the White House lawn, but a mom in Oak Park Michigan can’t do the same on her own private property? Insane.

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Asian Honey, Banned in Europe, Is Flooding U.S. Grocery Shelves

Posted on 15 August 2011 by admin

Asian Honey, Banned in Europe, Is Flooding U.S. Grocery Shelves

FDA has the laws needed to keep adulterated honey off store shelves but does little, honey industry says.

BY ANDREW SCHNEIDER | AUG 15, 2011

 

A third or more of all the honey consumed in the U.S. is likely to have been smuggled in from China and may be tainted with illegal antibiotics and heavy metals.  A Food Safety News investigation has documented that millions of pounds of honey banned as unsafe in dozens of countries are being imported and sold here in record quantities.
And the flow of Chinese honey continues despite assurances from the Food and Drug Administration and other federal officials that the hundreds of millions of pounds reaching store shelves were authentic and safe following the widespread arrests and convictions of major smugglers over the last two years.
Thumbnail image for honeycomb406.jpgExperts interviewed by Food Safety Newssay some of the largest and most long-established U.S. honey packers are knowingly buying mislabeled, transshipped or possibly altered honey so they can sell it cheaper than those companies who demand safety, quality and rigorously inspected honey.
“It’s no secret that the honey smuggling is being driven by money, the desire to save a couple of pennies a pound,” said Richard Adee, who is the Washington Legislative Chairman of the American Honey Producers Association.
“These big packers are still using imported honey of uncertain safety that they know is illegal because they know their chances of getting caught are slim,” Adee said.
Food safety investigators from the European Union barred all shipments of honey from India because of the presence of lead and illegal animal antibiotics.  Further, they found an even larger amount of honey apparently had been concocted without the help of bees, made from artificial sweeteners and then extensively filtered to remove any proof of contaminants or adulteration or indications of precisely where the honey actually originated.
An examination of international and government shipping tallies, customs documents and interviews with some of North America’s top honey importers and brokers documented the rampant honey laundering and that a record amount of the Chinese honey was being purchased by major U.S. packers.
Food Safety News contacted Suebee Co-Op, the nation’s oldest and largest honey packer and seller, for a response to these allegations and to learn where it gets its honey. The co-op did not respond to repeated calls and emails for comment. Calls and emails to other major honey sellers also were unreturned.
EU Won’t Accept Honey from India
Much of this questionable honey was officially banned beginning June 2010 by the 27 countries of the European Union and others. But on this side of the ocean, the FDA checks few of the thousands of shipments arriving through 22 American ports each year.
According to FDA data, between January and June, just 24 honey shipments were stopped from entering the country. The agency declined to say how many loads are inspected and by whom.
However, during that same period, the U.S. Department of Agriculture reported that almost 43 million pounds of honey entered the U.S. Of that, the Department of Commerce said 37.7 million pounds came from India, the same honey that is banned in the EU because it contained animal medicine and lead and lacked the proper paperwork to prove it didn’t come from China.
“There are still millions of pounds of transshipped Chinese honey coming in the U.S. and it’s all coming now from India and Vietnam and everybody in the industry knows that,” said Elise Gagnon, president of Odem International, a worldwide trading house that specializes in bulk raw honey.
The FDA says it has regulations prohibiting foods banned in other countries from entering the U.S. However, the agency said last month that it “would not know about honey that has been banned from other countries …”
Adee called the FDA’s response “absurd.” He said the European ban against Indian honey is far from a secret.
“Why are we the dumping ground of the world for something that’s banned in all these other countries?” asked Adee, who, with 80,000 bee colonies in five states, is the country’s largest honey producer.
“We’re supposed to have the world’s safest food supply but we’re letting in boatloads of this adulterated honey that all these other countries know is contaminated and FDA does nothing.”
The food safety agency said it’s doing the best it can with existing resources and will do more when the newly passed Food Safety Modernization Act is up and running.
Where Is Our Honey Coming From?
honeypot350.jpgThe U.S. consumes about 400 million pounds of honey a year – about 1.3 pounds a person. About 35 percent is consumed in homes, restaurants and institutions. The remaining 65 percent is bought by industry for use in cereals, baked goods, sauces, beverages and hundreds of different processed foods.
However, the USDA says U.S. beekeepers can only supply about a 48 percent of what’s needed here.  The remaining 52 percent comes from 41 other countries.
Import Genius, a private shipping intelligence service, searched its databases of all U.S. Customs import data for Food Safety News and provided a telling breakdown:
- The U.S. imported 208 million pounds of honey over the past 18 months.

- About 48 million pounds came from trusted and usually reliable suppliers in Argentina, Brazil, Canada, Uruguay and Mexico.

- Almost 60 percent of what was imported – 123 million pounds – came from Asian countries – traditional laundering points for Chinese honey. This included 45 million pounds from India alone.

“This should be a red flag to FDA and the federal investigators. India doesn’t have anywhere near the capacity – enough bees – to produce 45 million pounds of honey. It has to come from China,” said Adee, who also is a past president of the American Honey Producers Association.

Why Is Chinese Honey Considered Dangerous?
Chinese honeymakers began using various illegal methods to conceal the origin of their honey beginning in about 2001. That’s when the U.S. Commerce Department imposed a stiff tariff – as much as $1.20 a pound — on Chinese honey to dissuade that country from dumping its dirt-cheap product on the American market and forcing hundreds of U.S. beekeepers out of the business.
About the same time, Chinese beekeepers saw a bacterial epidemic of foulbrood disease race through their hives at wildfire speed, killing tens of millions of bees. They fought the disease with several Indian-made animal antibiotics, including chloramphenicol. Medical researchers found that children given chloramphenicol as an antibiotic are susceptible to DNA damage and carcinogenicity. Soon after, the FDA banned its presence in food.

“We need imported honey in this country.  But, what we don’t need is circumvented honey, honey that is mislabeled as to country of origin, honey that is contaminated with antibiotics or heavy metal,” said Ronald Phipps, co-chairman of the International Committee for Promotion of Honey and Health and head of the major honey brokerage firm CPNA International.
Heavy Metal Contamination
The Chinese have many state-of-the-art processing plants but their beekeepers don’t have the sophistication to match. There are tens of thousands of tiny operators spread from the Yangtze River and coastal Guangdong and Changbai to deep inland Qinghai province.  The lead contamination in some honey has been attributed to these mom-and-pop vendors who use small, unlined, lead-soldered drums to collect and store the honey before it is collected by the brokers for processing.
The amount of chloramphenicol found in honey is miniscule. Nevertheless, public health experts say it can cause a severe, even fatal reaction — aplastic anemia — in about one out of 30,000 people.
European health authorities found lead in honey bought from India in early 2010. A year later, the Indian Export Inspection Council tested 362 samples of honey being exported and reported finding lead and at least two antibiotics in almost 23 percent of the test samples.
The discovery of lead in the honey presents a more serious health threat.
“The presence of heavy metals is a totally different story, because heavy metals are accumulative, they are absorbed by organs and are retained. This is especially hazardous for children,” Phipps said.
All the bans, health concerns and criticism of Indian honey hasn’t slowed the country’s shipping of honey to the U.S. and elsewhere. In February, India’s beekeepers and its government agricultural experts said that because of weather and disease in some colonies, India’s honey crop would be late and reduced by up to 40 percent.
Yet two months later, on April 15 in Ludhiana, officials of Kashmir Apiaries Exports and Little Bee Group, India’s largest honey exporters, posed for newspaper photographers in front of “two full honey trains” carrying 180 20-foot cargo carriers with a record 8.8 million pounds of honey headed for the export ports.
“They’re clearly transshipping honey from China and I can’t believe that they are so brazen about it to put it right on the front page of a newspaper,” honey producer Adee said.

Data received by FSN from an international broker in India on Friday showed that within the last month 16 shipments – more than 688,000 pounds – of honey went from the Chinese port of Nansha in Guangzhou China to Little Bee Honey in India.  The U.S. gurus of international shipping documents – Import Genius – scanned its database and found that just last week six shipments of the honey went from Little Bee to the port of Los Angeles. The honey had the same identification numbers of the honey shipped from China.

Government investigators in the U.S. and Europe and customs brokers in India told FSN that previous successful criminal investigations had proven that the Chinese honey suppliers and their brokers are masterful at falsifying shipping documents.

Each of the shipments – whether from China or India – bore an identical FDA inspection number. However, FDA’s Division of Import Operations did not respond to requests for information on how and where it issued that FDA number.

Food Safety News left several messages for the Little Bee Group to discuss the source of their honey and how they were breaking records when the rest of India’s honey producers were months behind schedule. None of the phone messages or emails were returned.

Other major Indian honey exporters insist that India gets no honey from China. However, Liu Peng-fei and Li Hai-yan of the prestigious Chinese Academy of Agricultural Sciences disagree. In a scientific study of the impact the global financial crisis is having on China’s honey industry, the apiculture scientists wrote that to avoid the “punitive import tariffs” Chinese enterprises “had to export to the United States via India or Malaysia in order to avoid high tariffs…”

Why Hasn’t Smuggling Stopped?
The massive honey laundering scams that plagued the U.S. for more than a decade – the transshipment of Chinese honey to a second country before being reshipped to the U.S. — were presumably given a deathblow over the past two years.
During that period, Justice Department lawyers and Department of Homeland Security and FDA investigators launched a series of indictments and arrests of 23 German, Chinese, Taiwanese and American corporate officials and their nine international companies.
They were charged with conspiracy to smuggle more than $70 million worth of Chinese honey into the U.S. by falsely declaring that the honey originated from countries other than China. That allowed them to avoid paying stiff anti-dumping charges imposed on China.
It was an impressive series of complex busts spanning three continents, and instant fodder for a great whodunit novel. But, according to some of North America’s largest producers and importers of honey, the arrests bombed as a deterrent.
“There are still millions of pounds of transshipped Chinese honey coming into the U.S.A. and it’s all coming now from India and Vietnam. Everybody in the industry knows that,” said Odem International’s Gagnon.
How Do They Get Away With It?
When it comes to honey laundering, the crooks are always trying to stay one step ahead of the criminal investigators.

honeybarrels-inside.jpg

For example, when customs agents discovered that China usually shipped its honey in blue steel drums, the exporters quickly painted the drums green.
It took investigators a while to learn that often — while the drums were in port or en route at sea — the Chinese shuffled drum labels and phony paperwork showing country of origin as places that didn’t have an onerous anti-dumping tariff. The Russian Honey Federation blew the whistle on the Chinese relabeling millions of pounds as coming from Russia.
After that scam became known, the felons then shipped Chinese honey to countries like Vietnam, Indonesia, Malaysia and even Australia. There the honey was repacked, authentic local documents were issued and the honey was shipped on to the U.S. or elsewhere.
Another favorite con among Chinese brokers was to mix sugar water, malt sweeteners, corn or rice syrup, jaggery, barley malt sweetener or other additives with a bit of actual honey. In recent years, many shippers have eliminated the honey completely and just use thickened, colored, natural or chemical sweeteners labeled as honey.
However, sophisticated analysis that will match the pollen in honey to flowers from a specific geographic region is available at just two or three laboratories around the world.  There are also simpler, less expensive tests to detect the telltale presence of commercial sweeteners and other adulterants that are more readily available.
A laboratory in Bremen, Germany, founded a half century ago by German beekeepers, can accurately scan honey samples for flower pollen.   There is only one expert in the U.S. known to analyze pollen in honey to determine where it was actually grown and that would be at the Palygnology Laboratory at Texas A&M.  The lab was created and is run by Vaughn Bryant, a forensic palynologist and Professor of Anthropology.
Melissopalynology, or pollen analysis, has been used for years by geologists seeking evidence of ancient coastal areas – often sites of major oil deposits. Scientists tracing the origins of the Shroud of Turin have identified 61 different pollens on the cloth that could only have come from around Jerusalem.
Forensic scientists have used pollen identification to help solve murder, rapes, kidnapping and at least one espionage case. Now, at least in the labs in Texas and Germany, melissopalynologists use pollen to determine – with great accuracy – the geographic area where the bees foraged for the nectar.
“If they find, for example, pollen from flowers that grow in northern latitudes – like China – but it’s found in honey ostensibly produced in tropical countries – like India, Vietnam, Malaysia and the like – you know something’s rotten or illegal,” said CPNA International’s Phipps, who also produces a quarterly, international intelligence report that monitors the country-by-country supply of honey and everyone’s exports.
To avoid detection by concerned purchasers or criminal investigators, some Chinese producers in state-of-the-art processing plants pump the alleged honey, heated and under high pressure, through elaborate ceramic filters. This ultra-filtration removes or conceals all floral fingerprints and indicators of added sweeteners or contaminants.
“The Chinese have refined methods of masking their contaminated product by ultra-filtration so their honey seems perfect. But it’s not honey anymore. There’s no color.  There’s no flavor. There’s nothing.  So you take this perfect product, which could be confused with honey, and you blend it with real Indian honey,” Gagnon said.
“Everyone avoids tariffs because government agents cannot test to prove it’s from China.”

honeytesting-inside.jpgThe FDA says it has sent a letter to industry stating that the agency does not consider ultra-filtered honey to be honey.

“We have not halted any importation of honey because we have yet to detect ultra-filtered honey.  If we do detect ultra-filtered honey we will refuse entry,” said FDA press officer Tamara Ward.

“FDA is just not looking” was the answer that most honey brokers offered.  They added that the FDA doesn’t want to find it because then the agency would have to test for it, something it is incapable of doing in its existing laboratories.

Honey experts worry that new technologies will make detection of adulterants even more difficult.
At June’s conference of the Institute of Food Technologists in New Orleans, there were hundreds of Chinese vendors working in small clusters beneath bright red banners. They offered for sale almost any spice, food-processing substance or additives a food processor might want and promises of concocting anything else they could dream of. “All FDA approved,” they emphasized to potential clients.
One salesman quickly jerked back his business card when a reporter pulled out a tape recorder to capture the man’s promises offering a “nanoparticle sweetener for honey that cannot be detected.”
Does the FDA Care?
The U.S. Departments of Customs and Border Patrol and Immigration and Customs Enforcement have dollar and cents issues to worry about because hundreds of millions of dollars in unpaid taxes and anti-dumping tariffs on Chinese imports are circumvented by the honey laundering.
“These honey crimes are not a Republican or Democratic, Liberal or Conservative issue.  The country is being ripped off of millions and millions,” Phipps said.
Recent news releases by the border patrol and the FDA say they have developed an anti-smuggling strategy to identify and prevent smuggled foods from entering the United States and posing a threat to national security and consumer safety.
But at the field level, investigators with the two agencies and an agent with ICE’s Commercial Fraud Unit said the cooperation is more on paper then in practice and that the FDA continues to be the weak link. They say the FDA either doesn’t have the resources to properly do the job or is unwilling to commit them.
ICE and the border patrol can and do go after the honey launderers by enforcing the anti-dumping and tariff violation laws. But protecting consumers from dangerous honey, identifying it as adulterated and therefore illegal for importation, falls to the FDA. And many of its enforcement colleagues say the food safety agency doesn’t see this as a priority.
A Justice Department lawyer told Food Safety News that the FDA has all the legal authority and obligation it needs to halt the importation of tainted honey. He cited two sections of the agency’s regulations defining when food products are considered “adulterated.”
The regulations say: “Food is adulterated if it bears or contains a poisonous or deleterious substance which may render it injurious to health” and “damage or inferiority has been concealed.”
Those two factors pretty much sum up the health concerns that many have with the smuggled honey. But the honey industry and Congress can’t get the FDA to even come up with a legal definition of what honey is.
Eight years ago, America’s beekeepers and some honey packers petitioned FDA to issue an official definition of honey. Their concern was how to determine whether honey is bogus if there is no official standard to measure it against. The FDA did nothing.
Last Nov. 15, senators asked the food safety agency for the same thing. Again, nothing.
On Aug. 10, two members of the Senate Committee on Appropriations tried once more.
Sens. Kirsten Gillibrand (D-NY) and John Hoeven (R-ND) urged the FDA Commissioner Margaret Hamburg to issue the official definition.
Calling the lack of regulations “a food safety concern,” Gillibrand said a national standard of identity for honey is needed “to prevent unscrupulous importers from flooding the market with misbranded honey products…”
An investigator in FDA’s import section explained the agency’s refusal to develop an official definition to FSN. “If we had an official description of honey then FDA would have to inspect everything we’re importing to ensure it’s legal. That’s the last thing we want to do,” he said, but would not allow his name to be used because he wasn’t authorized to make public statements.
How Do You Stop The Illegal Flow?
Gagnon and four other major players in the honey industry have formed a voluntary group calledTrue Source Honey.  They hope it will eventually expand into an international, industry-wide program to certify the origin and quality of honey.
“We need an origin traceability program, a professional audit of both the exporters and the packers so those buying and selling honey can ensure its authenticity and quality,” said Gagnon, who is the group’s vice chairman.
Meanwhile, it’s rumored that the feds are increasing their surveillance of the large U.S. importers and not too soon, Adee and others say.
Adee likens the honey laundering to a huge auto chop shop, where the police occasionally arrest the low-level car thieves but others pop up to continue supplying the criminal operation, which authorities never go after.
“That’s what’s happening here,” Adee explained. “ICE and the other investigators have arrested a handful of the middle men, the brokers who supply the honey packers, but haven’t gone after the big operators buying the phony foreign honey.”
Adee and others interviewed by Food Safety News say there are 12 major honey packers in the U.S. and four or five that are involved with the bulk of illegal trade.
“We know who they are,” he said. “Everyone in the industry knows. If these packers are allowed to continue buying this possibly tainted but clearly illegal smuggled honey, the importers will always find a way to get it to them.”

———-

Editor’s Note:  Andrew Schneider, a two-time Pulitzer Prize-winning investigative reporter, writes for Food Safety News and The Food Watchdog.com

 

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Rawesome Foods Raid – SWAT Poured Out RAW Milk!

Posted on 03 August 2011 by admin

Rawesome Foods raid!

Cops poured out the milk!

(2683 views) Uploaded 8/6/2011 12:42:04 PM by HealthRanger

http://www.naturalnews.tv/v.asp?v=C39F34B67FDA804B2D94CD9BBA3F0A0A

Video Information

From the Rawesome Foods raid in Venice, California, this video is from the day of the raid and reveals how the government terrorists poured all the raw milk down the drain! Video courtesy of RealFoodRights.com

Video Keywords: food    health freedom    tyranny    raw milk    raw dairy    food freedom    rawesome foods   government raids

 

Health Ranger: ‘FDA fights organic farmers’

http://www.youtube.com/watch?v=EbE3SfvuL1g

 

 

(Rawesome Foods Raid) What Happened – by an employee


http://www.youtube.com/watch?v=KjmYOoa14XY

Rawesome Raid August 3, 2011

http://www.youtube.com/watch?v=lI1gvPmA_c8

 

Massive public protest announced against government-sponsored terrorism of Rawesome Foods in California

(NaturalNews) As promised, a massive public protest is now being announced to give the members of the public an opportunity to voice their outrage against today’s arrest of three raw foods advocates who are all being charged with conspiracy.

The protest will be held at the LA County Courthouse located at:
210 West Temple, Division 30
Los Angeles

Arrive there at 7:45 am to join the protest, which needs to be in full swing early, because the court hearing for James is scheduled at 8:30.

Please keep your protests non-violent in nature and bring your signs, shirts and more. LA newspapers and media have already indicated they will be on scene. NaturalNews video journalists will also be on the scene filming whatever goes down. Videos will be posted on www.NaturalNews.TV

Bring your own cameras, too, and record your own photos and videos. Please post on NaturalNews.TV and we will likely link to your video in upcoming coverage of this event.

We apologize for the very short notice of this public protest, but we are publishing details about this story as quickly as we can. The story is breaking big and has already reached millions of listeners on the Alex Jones Show (www.InfoWars.com) and millions of readers through the Drudge Report (www.DrudgeReport.com), which has linked to NaturalNews as the breaking news source for this story.

Once the mainstream media starts covering this story, they will twist it around and LIE about it as they always do. NPR already did a hatchet job on this group following a previous raid. Only independent media (like NaturalNews) can be trusted to bring you the honest story on this without some corporate or government agenda.

There are already misinformed accusations that Rawesome Foods was not licensed as a retail business. But that’s incorrect information: Rawesome Foods is a private buying club and not a retail business that’s open to the general public. People can’t just walk in off the street and shop there like a regular grocery store. Thus, Rawesome does not have to be licensed like a regular grocery store. They are a private buyer’s club.

What went down in Venice, California today was clearly an act of government-sponsored terrorism against innocent citizens who are only “guilty” of selling healthful foods that are in huge demand by happy, healthy members (customers). That the selling of healthful raw milk cannot even be tolerated by the thuggish, corrupt government criminals who run the state of California (and the federal government) today is a powerful statement of just how much freedom we’ve already lost… and how hard we’re all going to have to fight back against tyranny to restore our basic food freedoms.

Watch NaturalNews for more developments on this story, and thank you for spreading the word about this latest assault on food freedom in America.

Learn more: http://www.naturalnews.com/033223_Rawesome_Foods_public_protest.html

 

“Rawesome” Raw Milk Farm Raided…Again

Rawesome Foods Co-Op

It has been reported this morning (August 3rd, 2011), that raw milk farm “Rawesome” in Venice, California has been raided once again by members of the SWAT team. With guns drawn, two of the owners arrested, and over $10,000 worth of raw milk dumped out, the freedoms of Americans are diminishing. There is, however, something we can do about it.

Rawesome Raid – Based on Public Health?

The excuse given for these absurd raids (that honestly casts embarrassment over the police force) is that raw milk is a health threat that causes listeria, e. coli disease and death. This certainly can be true for raw milk — but only if you are drinking raw milk from animals that are being raised in inhumane and poor conditions.

The actual excuse for the arrests and the raids have not yet been officially stated. Stay tuned for that news.

Clean, fresh raw milk from grass fed, free ranging animals, however, does not need to be pasteurized. Milk you purchase from a traditional grocery store does require pasteurization, as the farmers who raise these cows raise them in poor, dirty and sanitation conditions. Pasteurization is the answer for man’s dirty mistakes! Nature does not need to be cleaned, and man does not know more than nature.

Raw Milk Proven Safer than Other Commonly Sold Foods

Recent data from researcher Dr. Ted Beals, M.D., shows that between 1999 through 2010 illnesses resulting in raw milk consumption totaled to around462, which is about 42 illnesses per year. Out of the 47.8 million food borne illnesses each year from foods such as raw meat (which is readily available at every grocery store), peanut butter and spinach, it is very curious as to why raw milk is targeted so violently.

Up to 2011, it is estimated that close to 10 million individuals drink raw milk as its popularity rises. More and more individuals are starting to realize and wake up to the fact that are rights as citizens, when it comes to what we consume or inject in our bodies, are slowly being taken away.

We are supposed to be free. We are supposed to be able to make informed decisions on our health. With the majority of the population overweight, diabetic and prediabetic, shouldn’t we focus more attention on the foods that are actually threatening the health of the American population? Shouldn’t we be performing raids on sugary cereals that surpress immune function and accelerate cancer growth, learning disorders and blood sugar instability?

Read Natural News’ article on the illegal actions of the SWAT members and the raid.

http://thehealthyadvocate.com/2011/08/03/rawesome-raw-milk-farm-raided-again/

 

Breaking news: Multi-agency armed raid hits Rawesome Foods, Healthy Family Farms for selling raw milk and cheese

(NaturalNews) This is a NaturalNews exclusive breaking new report. Please credit NaturalNews.com. A multi-agency SWAT-style armed raid was conducted this morning by helmet-wearing, gun-carrying enforcement agents from the LA County Sheriff’s Office, the FDA, the Dept. of Agriculture and the CDC (Centers for Disease Control).

This story is now being followed and widely reported on InfoWars (www.InfoWars.com) and the Drudge Report (www.DrudgeReport.com). See updates below…

Rawesome Foods, a private buying club offering wholesome, natural raw milk and raw cheese products (among other wholesome foods) is founded by James Stewart, a pioneer in bringing wholesome raw foods directly to consumers through a buying club. James was followed from his private residence by law enforcement, and when he entered his store, the raid was launched.

Law enforcement demanded that all customers (members) of the store vacate the premises, then they demanded to know how much cash James had at the store. When James explained the amount of cash he had at the store — which is used to purchase product for selling there — agents demanded to know why he had such an amount of cash and where it came from.

James was handcuffed, was never read his rights and was stuffed into an unmarked car. While agents said they would leave behind a warrant, no one has yet had any opportunity to even see if such a warrant exists or if it is a complete warrant.

Law enforcement then proceeded to destroy the inventory of the story by pouring the milk down the drain and / or confiscating raw cheese and fresh produce for destruction. Video now posted at NaturalNews.TV: http://www.naturalnews.tv/v.asp?v=A…

Note to NaturalNews readers: We believe this was an ILLEGAL raid being conducted mob-style by government thugs who respect no law and no rights. This is an all-out war by the government against people who try to promote healthy raw and living foods.

James is now being held at the Pacific division police department at Centinela and Culver in Los Angeles. He is being held at $123,000 bail with no possibility of using bail bonds. Law enforcement has demanded that if he comes up with the money to cover bail, he must disclose to them all the sources of that money. (This is an illegal demand!)

Massive public protests are needed to teach these criminal law enforcement agencies that they cannot illegally arrest and persecute individuals merely for buying and selling raw milk and cheese. We are organizing a public protest day in cooperation with James. Please watch NaturalNews for an announcement of that. Story is developing…

Right now, James needs help raising money with his legal defense needs. Our non-profit Consumer Wellness Center is currently serving as the collection point for donations. You may donate right now at www.ConsumerWellness.org (100% of the donations go directly to James’ legal defense needs, the Consumer Wellness Center keeps nothing).

See this video of James Stewart talking about his farm:

http://www.youtube.com/watch?v=foKg…

Story on InfoWars.com:

http://www.infowars.com/raw-food-ra…

Here’s background on Healthy Family Farms which was also targeted in the raid:

Healthy Family Farms in Santa Paula, California:

“Healthy Family Farms is a sustainable, pasture-based farming operation. We raise all our livestock on pasture. We raise all of our animals from birth. We do not feed any of our animals soy, choosing instead to feed animals as they are designed to be fed. This results in healthy, sturdy animals needing no hormones, antibiotics, or other artificial “enhancements.” We harvest our animals humanely by hand before they are delivered to the farmers markets. We never freeze our products. In addition to farmer’s markets sales, we have an active CSA, which offers discounts to our valued members.”

Watch NaturalNews.com for more breaking news on this story. We are fed up with these illegal mob-style raids against the raw foods community! It is time to protest and fight back against tyranny!

Learn more: http://www.naturalnews.com/033220_Rawesome_Foods_armed_raids.html

 

Rawesome Foods founder to be prosecuted under special environmental crimes unit in LA

(NaturalNews) Details are still sketchy on this, as we’re breaking this news straight from the front lines in the aftermath of the government raid on Rawesome Foods in Venice, California (http://www.naturalnews.com/033220_R…), but NaturalNews is now being told that the LA County District Attorney will not be prosecuting James Stewart and the other “conspirators” who were arrested yesterday for selling raw milk. Instead, a special “environmental crimes” prosecutor will reportedly be prosecuting the case, which now consists of 13 criminal charges, some of which are felony crimes.

NaturalNews has not yet learned the name of this special environmental prosecutor, but the explanation smacks of the new environmental police who have been promoted through various propaganda outlets as being upstanding protect-the-Earth cops who arrest people for burning too much gas or using non-recyclable cups to drink beverages.

The issue of environmental police has been covered extensively by Alex Jones at InfoWars.com, where he refers to them as eco fascists. See this page to read more about how propaganda ads are being used to get people comfortable with the idea that “environmental crimes” should result in police slamming your face into the ground and handcuffing you:

http://www.infowars.com/audis-eco-f…

The videos on that page have been disabled, but here’s an alternate link of the green police Superbowl Ad:
http://www.youtube.com/watch?v=Wq58

(Astonishing ad. You MUST watch it.)

The real aim of the green police agenda

Far from being a campaign merely to protect the Earth (which would be great if it were true), the new “green police” agenda is now being used as a way to terrorize innocent Americans as we’re seeing right now with Rawesome Foods. What’s especially frustrating about all this is that some of the Al Gore followers who largely supported the idea of the green police are, in fact, the very same people who are now being targeted for advocating raw milk. They had been misled, sadly.

You see, eco fascism was never really about protecting the planet and promoting sustainable living. It was always about enslaving the population, destroying health freedom, and mandating total corporate conformity at gunpoint. That’s the lesson we’re now learning from the Rawesome Foods raids, where LA County Sheriffs literally poured thousands of dollars worth of wholesome raw milk down the drain and arrested the buying club owner who will be prosecuted as by a special environmental prosecutor.

For the record, I’m a huge advocate of green living, renewable energy, and green consumer practices — but NOT at the cost of surrendering our Constitutional freedoms to a group of government badge-wearing eco terrorists who raid our raw milk clubs and charge people with conspiracy crimes for “mislabeling cheese.” I believe in solar power, I raise my own chickens and grow a portion of my own food NOT because Al Gore told me to, but because it just makes common sense in today’s unpredictable world to be prepared for food supply disruptions and power grid failures.

I try to minimize my eco-footprint on the planet not because some bureaucracy forces me to, but because I want to support the long-term continuation of sustainable life on our planet. Yes, I’m “green” in my daily practices, and at the same time I’m strongly invested in the powerful ideas of liberty and freedom for individuals. “Green” should never mean we have to mean we give up our freedoms. Forcing people to “go green” at the end of a gun isn’t acceptable. It must be done through education and awareness.

Green cops are no better than regular corrupt cops

It’s very clear to me that much of the political talk about saving the planet and going green was really just a campaign to encourage people to surrender their freedoms to yet another tyrannical enforcement bureaucracy that will abuse its power just like every other government agency abuses its power. “Green police” is just another excuse to put tens of thousands of new badge-wearing power trippers on the streets who will terrorize innocent citizens.

And that’s really, really sad, because I think the core idea of “going green” in our day-to-day lives is extremely valuable and valid. We should stop pouring toxic chemicals down the drain. We should collect rainwater and drink that instead of drinking toxic city water. And for that matter, our own government should stop dumping toxic fluoride chemicals into the water supply in the first place!

Meanwhile, the real environmental threats to our planet — such as the Fukushima meltdowns, the toxic chemicals produced by Big Pharma, and the DNA contamination of our planet with GMOs — remains totally ignored. That’s how this game always works: The big corporate criminals run free while the little people are persecuted in the name of “green.”

How insane is it, really, that this raw milk and cheese buyer’s club is now being prosecuted by the very same people who were given power by the green police movement?

All I can say is, beware of creating new police in any form, because when you create police, military or political forces that have power of your lives, they will ALWAYS abuse that power. Eventually, every bureaucracy or institution becomes totally corrupted by corporate influence, and then it no longer serves the people but the corporatocracy that really runs the show.

Notice that all the wealthy elite who pay no corporate taxes and fly around in private jets aren’t being targeted for arrest by the green police? There’s a reason for that. The whole campaign is designed to muzzle the little guy and remind the slaves that they’re really just slaves.

Pay attention, SLAVE. Drink your dead pasteurized milk, take your psychotropic drugs, gulp down your fluoridated water and shut the hell up. You’re under the control of the new eco fascists now, and it’s no longer just talk. It’s all coming to a farm near you.

Learn more: http://www.naturalnews.com/033233_green_police_environmental_crimes.html

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FDA is Considering Adding Agent Orange to Your Dinner Plate

Posted on 02 July 2011 by admin

Total Video Length: 1:12:45
Download Interview TranscriptHere, Andrew Kimbrell, Executive Director of the Center for Food Safety since 1997, and one of the United States’ leading environmental attorneys, shares his ideas about the ideal future of food.

Visit the Mercola Video Library

Dr. Mercola’s comments:

Mr. Kimbrell is one of the United States’ leading environmental attorneys, and an author of articles and books on environment, technology and society, and food issues. He’s also the Executive Director of the Center for Food Safety, which he founded in 1997 as a way to prevent genetic engineering and sewage sludge remediation from becoming acceptable practices under the organic laws.

Organics and Beyond

But the Center for Food Safety has far grander goals than simply fighting for pro-organic laws.

“[W]e call it “Organic and Beyond,” Kimbrell says.

“We do that because we have to defend the organic standards. Over the last eight years, virtually the entire government’s all three branches, from judiciary to executive to congress, were trying to undermine the organic rule. It didn’t get as much publicity as it should have…

But we don’t want just to defend the organic rule in food. We want to evolve the ethic.

While organic is great and we need to defend that, we also want to make sure that we extend it to include for instance issues of animal welfare… We want to have bio-diverse crops… We want to make sure that our farming is local, in appropriate scale. We also want to make sure that we’re socially just. Just because we’re organic it doesn’t mean that we’re treating farm workers in a socially just manner.

Those are the beyond organic aspects of the future of food that we’re really interested in, which is a humane, local, appropriate scale, biodiverse, and socially just [system].

If we can think of the organic not as the ceiling for our food in the future but as the floor and we build this house, our future food house with those other elements… then I think we really will have done something.”

Saying “No” to Some Things is Saying “Yes” to Others

As you probably know, we are inundated with tens of thousands of chemicals these days, which have never before existed on Earth—many of which are extremely toxic. Much of the rise in chronic disease can be traced back to the excessive exposure to toxins from our food, air, water supply, and many of the personal- and household products we use on a daily basis.

What led us to this point?

In a word, technology.

For all the benefits and wonders many technologies bring, there are also some profound downsides, especially when they’re introduced without proper safety testing and forethought of the long-term consequences. Nuclear energy is just one glaring recent example. But this applies to food as well, as biotech has crept in to modify nature’s bounty in all sorts of ways, and mass-producing farms have altered the way food is grown to include massive amounts of chemicals.

“[O]rganic is really amazing because organic says: we’re looking at chemicals, and fertilizers and pesticides and we’re saying no. We’re looking at genetic engineering and we’re saying no. We’re looking at irradiated foods and we’re saying no,” Kimbrell says.

“We’re saying, progress sometimes means saying no to these technologies and saying yes to a far more natural, a far more sustainable way of doing business. It’s quite a remarkable revolution, not just because of the food, but because of the consciousness.

It’s saying progress doesn’t mean more and more exploitation and manipulation of nature through technology, it means more and more integrating the human into the entire natural context and learning to live within that context.”

“We Defend what We Love”

Kimbrell’s passion for this work stems from learning to love nature through his brother, who was an avid outdoorsman. He also worked on a farm for two and a half years before going to law school, and while he loved it, he wasn’t very good at it. The farmer he worked for suggested he go to law school instead, and “see what you can do for farms and for the whole community of life that makes for a healthy farming system.”

It turned out to be good advice. Some of his first work as an environmental attorney was in defending rivers and natural areas from exploitation, which, over time “evolved into an understanding of how technologies were hurting the natural world.”

“Those two things – my love of the natural world and my work on a farm– sort of coalesced, if you will, to create my desire to use my legal skills and whatever skills we have, to accomplish the goals that we just talked about,” Kimbrell says.

Food and the Environment

As Kimbrell states in this interview, food is the most intimate relationship you have with your environment.

“I’m always amused when people say, I’m not interested in food issues, I’m interested in environmental issues. I would say, “Whoa, let’s sit down for a second to talk about that.” There is no more intimate relationship that we have with the environment than what we eat.

To me it is a great moment for everybody out there to say, ‘I’m making a choice every day—a choice that I can control to a great extent—of what I eat, what my family eats, and to a certain extent what people around me eat.

That is to me a really important moment, because in that moment, you can reflect your views on social justice, your views on animal welfare, your views on the environment, on protecting our waters, protecting our air, protecting our soil, protecting our farm communities and protecting our community health. All of that is based in that decision that we all make several times a day.”

The Dangers of Genetically Modified Foods

From Kimbrell’s perspective, as well as my own, genetically modified (GM) food is one of the biggest threats to life and health we currently face on this planet.

“It turns out that [genetic engineering] is a lot more difficult than people thought,” Kimbrell says. “There are a couple of reasons for that. For example, folks may remember the Human Genome Project. We were supposed to have about 100,000 to 140,000 genes. We only have about 20,000 genes it turns out. That’s about as many as a worm.

A kernel of corn has, any cell on that kernel has 35,000 genes… They just did the genome of wheat and it has 80,000 genes. So wheat has four times as many genes as humans.

It turns out that the biology of these crops isn’t some simple thing but extremely complex and it turns out there is a huge amount we do not know. So this idea that you can take a little piece of DNA called a gene and switch it around between plants and animals, and human and plants, and bacteria and plants, and get predictable results turn out not to be true.”

At the present time, the most prominent genetic modification of crops is the modification to make plants immune to herbicides.

Since you can spray these crops with large amounts of chemicals without killing the crop, this, in theory, should significantly reduce weed growth. However, in the years since the introduction of “RoundUp ready” corn and soy, we’ve witnessed increasingly profound downsides to these unnatural seeds, including brand new “super weeds” that are also impervious to RoundUp (glyphosate).

According to Kimbrell, we now have 10-20 million acres of these super weeds that you can’t kill. They’re the thickness of a baseball bat, and they loom six to seven feet tall!

GM Crops Demand HIGHER Levels of Toxic Herbicides and Pesticides

Additionally, what many fail to realize is the incredible increase in toxic chemicals being used on these crops, which eventually ends up in your stomach.

“[I]n the last two years we’ve sprayed 153 million more pounds of herbicide on our crops because of the corn and soy Roundup-ready crops…” Kimbrell says.

This dilemma is leading us further and further into a quagmire of increasingly toxic remedies.

“Right now, the FDA is looking to approve crops resistant to 2,4-D, which is an element in Agent Orange,” Kimbrell says. “I kid you not, Dow Chemical is doing this. Corn and soy that has been genetically engineered so you can spray as much 2,4-D (Agent Orange) on these crops as you want and it won’t kill them.

Now that Roundup is becoming less and less useful, they’re looking for newer and more toxic herbicides that they will bathe our crops in, in order to make money…

Monsanto is now coming up with Dicamba, which is extremely dangerous. It’s a volatilizing herbicide. In other words, you spray it and under certain weather conditions it’s going to go back up from the ground, re-volatilizing to a cloud and it could go a mile or two away and come back down and it will kill everything green. It’s a very toxic herbicide.”

This poses tremendous challenges for organic farmers, threatens our environment and human health everywhere, whether you happen to live in an agricultural area, or simply eat the food produced from these now highly toxic crops.

  • Where is the breaking point?
  • When will the food produced become too toxic to eat?
  • And what do we do then?

GM Foods Line the Pockets of Chemical Companies

There can be little doubt that the technology of genetically engineered crop seeds has little to do with saving the planet, and a lot to do with promoting herbicide use and increasing herbicide sales. The major purveyors of GM crop seeds also make the chemicals and herbicides to go along with those seeds.

These companies include:

Monsanto Dow Dupont
Syngenta Bayer BASF

“These are herbicide companies that have invented a way to sell a lot more of their chemicals,” Kimbrell says.

In the end, we may be over-run with superweeds that cannot be killed even by dousing it with Agent Orange, and GM crops that contaminate all its conventional and organic counterparts. That will be their legacy to our children and grandchildren…

Only Sustainable, Smaller-Scale Farming Can Successfully Feed the Planet

“I think one of the great things about the Organic and Beyond movement is that we are trying to go back and learn,” Kimbrell says. “We can use some modern technologies that help us better understand agronomy, but basically go back into a sustainable, smaller, more localized farming system.

What makes this so great is that two studies just came out of the UN, and it turns out that the way to feed the world is through small and medium sized organic and sustainable farms because they are creating a lot more food!

Right now, we have so many acres devoted to corn but you cannot live on corn alone. As a matter of fact you shouldn’t be living on much corn at all really. That’s not really food. That’s a crop. It’s a crop that’s used to feed animals, for biofuels and for fructose corn syrup and other additives.

Small medium sized farms have numerous diverse crops and animals. It’s a far more sustainable way to not produce massive crops but actual food.”

Change is an Uphill Battle that Oftentimes Requires Litigation

Unfortunately, despite the evidence showing that our current agricultural system is unsustainable, if not downright dangerous, change is hard to come by. The agricultural committees are primarily run by the agribusiness industry, which will always vote to protect their own best interests.

One effective way to slow down the madness, as it were, is through litigation. According to Kimbrell, litigation has halted the introduction of a number of genetically engineered crops, such as GM:

  • Wheat
  • Rice
  • Bentgrass

Market campaigns also successfully thwarted the introduction of GM tomatoes and potatoes.

“We can vote with our dollar in the marketplace by buying organic, by buying non-GMO,” Kimbrell says. “But we can also then make sure that we use the courts as best we can to halt some of these damaging technologies while we promote this Organic and Beyond vision. And everyone can get involved.”

Current Campaigns to Eliminate GMOs

The Center for Food Safety, along with a number of other organic businesses, organic organizations, and non-governmental organizations, are now starting a campaign to demand labeling of all GM foods.  This is the most sensible strategy as over 90 percent of the public do not want GM foods and if they had a choice they would avoid Them. We don’t need legislation to outlaw GM, we just need an informed public to make the right choice.

Genetically engineered foods are required to be labeled in the 15 European Union nations, Russia, Japan, China, Australia, New Zealand, and many other countries around the world, but not the US or Canada…

“You’re looking at a food that offers you risk and no benefits. It is true because the companies and the government have never looked at it. We don’t know the exact extent of that risk but we know the risk is there.

What rationale person would ever pick a food if it was labeled? … The GMO offers me no additional benefits, and only additional health risks. What would you choose?

No one is going to choose the GMO version. That’s why they don’t want labeling.”

Another very important aspect of labeling is traceability of health effects. This can literally become a life and death issue. This is yet another reason why the industry is fighting tooth and nail to avoid labeling, because they know that without labeling it’s virtually impossible to trace any health effects that may be associated with the GM ingredients. This releases them from liability.

During the Presidential campaign of 2008, Obama put in writing a promise to support mandatory labeling on GMOs.

It’s time to hold him to that promise!

I urge you to sign the petition for mandatory labeling, and to share it with everyone you know!

Also, if you don’t already have a copy of the Non-GMO Shopping Guide, please print one out and refer to it often. It can help you identify and avoid foods with GMOs. Also remember to look for products (including organic products) that feature the Non-GMO Project Verified Seal to be sure that at-risk ingredients have been tested for GMO content. Many health food stores will carry these products.

You can also download the free iPhone application that is available in the iTunes store. You can find it by searching for ShopNoGMO in the applications.

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International Codex Alimentarius Symposium Belgium

Posted on 29 December 2010 by admin

International Codex Alimentarius Symposium Belgium

Main Speakers: Scott Tips & Ian Crane

 

The Symposium was held in Ghent, Belgium on 29th of November 2009, organized by the Belfort Group, Citizens In Action Belgium:

http://citizensinactionbelgium.ning.com

http://belfort-group.eu

 

Here was the introduction clip & the 18 clips are the symposium itself, please watch & share the very important information..

http://youtube.com/watch?v=yq7z8HloV2o

 

Main Speakers:

Scott Tips:

http://thenhf.com/page.php?id=140

Ian R. Crane:

http://ianrcrane.co.uk/

Jolanda de Groot:

http://www4.dr-rath-foundation.org

 

Love is the Only Engine of Survival..

 

Belfort Group Codex Alimentarius Symposium:

 

1/18 = http://youtube.com/watch?v=EbXjKBG2xHU

2/18 = http://youtube.com/watch?v=CT1a8qHc3IA

3/18 = http://youtube.com/watch?v=21zy8dMiNOE

4/18 = http://youtube.com/watch?v=0rl6hhPFNXE

5/18 = http://youtube.com/watch?v=_vpeXKHWVY4

6/18 = http://youtube.com/watch?v=O016xpzBTUo

7/18 = http://youtube.com/watch?v=NkQEbRUWJm8

8/18 = http://youtube.com/watch?v=N_oXbXUmD7s

9/18 = http://youtube.com/watch?v=K8kO5wjJcFs

10/18 = http://youtube.com/watch?v=sxCc5LYsGCU

11/18 = http://youtube.com/watch?v=9O_aa3LN2a4

12/18 = http://youtube.com/watch?v=XY7znLcl9lk

13/18 = http://youtube.com/watch?v=2FvjRbMVxTs

14/18 = http://youtube.com/watch?v=sp4kItmdi24

15/18 = http://youtube.com/watch?v=0c97T682vng

16/18 = http://youtube.com/watch?v=fjDubu-64YM

17/18 = http://youtube.com/watch?v=SIl_aL7Tp7c

18/18 = http://youtube.com/watch?v=9M5nAMuqLqI

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International Codex Alimentarius Symposium Belgium

Posted on 29 November 2010 by admin

International Codex Alimentarius Symposium Belgium

Main Speakers: Scott Tips & Ian Crane

The Symposium was held in Ghent, Belgium on 29th of November 2009, organized by the Belfort Group, Citizens In Action Belgium:

http://citizensinactionbelgium.ning.com

http://belfort-group.eu

Here’s the introduction clip & the 18 clips are the symposium itself, please watch & share this very important information:

http://youtube.com/watch?v=yq7z8HloV2o

Main Speakers:

Scott Tips: http://thenhf.com/page.php?id=140

Ian R. Crane: http://ianrcrane.co.uk/

Jolanda de Groot: http://www4.dr-rath-foundation.org

Belfort Group Codex Alimentarius Symposium:

1/18 = http://youtube.com/watch?v=EbXjKBG2xHU

2/18 = http://youtube.com/watch?v=CT1a8qHc3IA

3/18 = http://youtube.com/watch?v=21zy8dMiNOE

4/18 = http://youtube.com/watch?v=0rl6hhPFNXE

5/18 = http://youtube.com/watch?v=_vpeXKHWVY4

6/18 = http://youtube.com/watch?v=O016xpzBTUo

7/18 = http://youtube.com/watch?v=NkQEbRUWJm8

8/18 = http://youtube.com/watch?v=N_oXbXUmD7s

9/18 = http://youtube.com/watch?v=K8kO5wjJcFs

10/18 = http://youtube.com/watch?v=sxCc5LYsGCU

11/18 = http://youtube.com/watch?v=9O_aa3LN2a4

12/18 = http://youtube.com/watch?v=XY7znLcl9lk

13/18 = http://youtube.com/watch?v=2FvjRbMVxTs

14/18 = http://youtube.com/watch?v=sp4kItmdi24

15/18 = http://youtube.com/watch?v=0c97T682vng

16/18 = http://youtube.com/watch?v=fjDubu-64YM

17/18 = http://youtube.com/watch?v=SIl_aL7Tp7c

18/18 = http://youtube.com/watch?v=9M5nAMuqLqI

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Addition of National Toxicology Program Carcinogens

Posted on 26 November 2010 by admin

EPA has finalized a rule to add 16 chemicals reasonably anticipated to be human carcinogens to the TRI list of reportable chemicals. This action is part of the Agency’s ongoing efforts to examine the scope of TRI chemical coverage and provide communities with more complete information on toxic chemical releases. It is the largest chemical expansion of the program in over a decade.

 

Addition of National Toxicology Program Carcinogens – Final Rule

On November 26, 2010, EPA finalized a rule to provide communities with additional information about toxic chemicals being released to the environment. The rule, which will be effective on November 30, 2010, adds 16 chemicals to the TRI list of reportable chemicals. This action is part of EPA’s ongoing efforts to examine the scope of TRI chemical coverage and provide more complete information on toxic chemical releases, and it is the first TRI program chemical expansion in over a decade.

Each chemical that EPA is adding has been classified as “reasonably anticipated to be a human carcinogen” by the National Toxicology Program (NTP) in their Report on Carcinogens (RoC) document. EPA has concluded, based on a review of available studies, that these 16 chemicals could cause cancer in humans and therefore meet the EPCRA section 313(d)(2)(B) statutory listing criteria.

Four of the chemicals are being added to TRI under the polycyclic aromatic compounds (PACs) category. The PACs category is of special concern because PACs are persistent, bioaccumulative, toxic (PBT) chemicals and as such, they are likely to remain in the environment for a very long time, are not readily destroyed, and may build up or accumulate in body.

Addition of National Toxicology Program Carcinogens; Community Right-to-Know Toxic Chemical Release Reporting:

Final Rule (PDF, 8pp, About PDF)

Proposed Rule

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S 510 and Codex Alimentarius – the removal of nutrition

Posted on 20 September 2010 by admin

by A. Goodwin

S 510 includes passages that would force harmonization with Codex Alimentarius. It is a name most people do not know and one that the media has not exposed though its consequences to human health would be extreme. Codex threatens the lives of millions through limiting access to adequate supplementation.

From an open letter by Dr. Matthias Rath, a renowned cardiologist, sent to Helmut Kohl, the German chancellor and one time pharmaceutical lobbyist who introduced Codex to the world.

This “Codex” Commission is overwhelmingly composed of representatives of German and international pharmaceutical corporations, and its aim is to set world-wide guidelines for vitamins, amino acids, minerals and other dietary supplements. Spearheaded by the German pharmaceutical corporations, this Codex Commission plans to ban, on a world wide scale, any health statements in relation to vitamins, be it preventive or therapeutic. Moreover, the only vitamin formulas which would still be available would have to meet the arbitrary restrictions of the Codex Commission. The nations that do not comply with these restrictions are faced with economic sanctions.

These plans of the pharmaceutical corporations and the Codex Commission are in direct opposition to the overwhelming importance of vitamins and other essential nutrients for human health and, in particular, for preventing cardiovascular disease. …

With this background, the attack of the Codex Commission is a desperate act by pharmaceutical companies to protect their world-wide drug market against naturally effective and much more affordable vitamins. Particularly disturbing is the spearheading role of the German pharmaceutical corporations within the Codex Commission. Once before in this century, a German pharmaceutical and chemical corporation, I.G. Farben, became responsible for the deaths of millions of people and consequently, was dismantled in 1946 by the Nuremberg Tribunal and split into Bayer, BASF and Hoechst. With the current plans of the German pharmaceutical companies, the predictable dimension of the unnecessary and premature death of millions of people is unavoidable. If the Codex Commission is allowed to obstruct the eradication of heart disease by restricting access to nutritional supplements, more than 12 million people world-wide will continue to die every year from premature heart attacks and strokes. Within the next generation alone, this would result in over 300 million premature deaths, more than in all the wars of mankind together.

 

Codex for the US began on December 31, 2009. There have been five bills so far this year to remove access to supplements, if one adds S 3767 introduced by Senators Leahy, Klobuchar, and Franken on September 13th.

How dangerous are supplements that they are subject to FDA armed raids?

The Hazardous-Nutritional-Supplements -Target of FDA Police Raids:

Annual Deaths From:

FDA-Approved Drugs (1)…….60,000 – 140,000

Food Contamination (2)………………………9,100

Aspirin (3)………………………………………………90

All vitamins (4). …………………………………….. 0

Uncontaminated amino acids (4)………………0

Commercial herbs (4)……………………………… 0

 

Why is this happening? The logic is inescapable - illness is worth money and health is worth $0. The FDA would be in charge of whatever agency is set up under S 510 (and S 3767) which would destroy availability of adequate nutrition. The dark history of the FDA’s work to cut off knowledge of and access to all treatments for cancer not coming from the pharmaceutical industry is extensive but mostly unknown. The current FDA, pleading it doesn’t have enough power to stop food contamination, finds power when it comes to stopping gentle cancer treatments and safe treatments for pain, and loses it again when it comes to drugs causing thousands of heart attacks ordeaths and is silent on common pharmaceutical industry pain medications which routinely kill.

The value of supplements is abundantly clear to the pharmaceutical industry. When they were the main support for Germany during WWII, it was “A crime punishable by death to spread information in regard to nutrition in Norway, Belgium, Holland, and all other conquered countries.” - D.T. Quigley, MD, Fellow American College of Surgeons, in The National Malnutrition

Today, the FDA is involved in an on-going, unconstitutional effort to stop information about theeffectiveness of supplements, especially those which offeralternatives to H1N1 vaccines. The FDA has been and is increasing its removal of freedoms around speech, and health (as relates to food and vaccines/drugs), and now, just as they hope to control vast power over food and remove supplements, has gone so far as to assert in court that there is no fundamental right to one’s bodily and physical health. (Is this a necessary legal accompaniment to the devastation that Codex would cause, and to forcing people into exposure to pharmaceutical industry’s vaccines which have become increasingly unsafe?)

 

The removal of rights is the focus of

this video on Codex: “We Become Silent – The Last Days of Health Freedom” with Dame Judy Dench.

 

While people may sense that the consequences of the removal of nutritional supplements would be serious, it is possible to see in advance what would result from Codex-compelled vitamin and minerals deficiencies. In viewing the list, however, it is important to realize that those born or already sick with diseases and certain groups such as children, pregnant women and the elderly would be impacted first, given their greatly elevated requirement for nutritional supplementation. And hyper-supplementation to actually treat diseases would be available. Adults who do not fall into those categories would became ill from lack of adequate nutrition, at which point they would join the ranks of the ill and their own nutritional requirements to sustain lives would go up.

This following list is brief, not including hundreds herbs or any of the specially combined nutritional formulations, including those with absolute evidence of their effectiveness, and the absence of which

 

Vitamin D

http://www.amjmed.com/article/S0002-9343(09)00440-9/fulltext

From the American Journal of Medicine:

“Adequate vitamin D status is necessary and beneficial for health, although deficiency plagues much of the world’s population. In addition to reducing the risk for bone disease, vitamin D plays a role in reduction of falls, as well as decreases in painautoimmune diseasescancerheart disease, mortality, and cognitive function. On the basis of this emerging understanding, improving patients’ vitamin D status has become an essential aspect of primary care. Although some have suggested increased sun exposure to increase serum vitamin D levels, this has the potential to induce photoaging and skin cancer, especially in patients at risk for these conditions.Vitamin D deficiency and insufficiency can be both corrected and prevented safely through supplementation.”

 

Vitamin A deficiency

http://en.wikipedia.org/wiki/Vitamin_A_deficiency

Vitamin A deficiency is a lack of vitamin A in humans. It is common in developing countries but rarely seen in developed countries. Night blindness is one of the first signs of vitamin A deficiency.Xerophthalmia and complete blindness can also occur since Vitamin A has a major role in phototransduction. Approximately 250,000 to 500,000 malnourished children in the developing world go blind each year from a deficiency of vitamin A, approximately half of which die within a year of becoming blind. The United Nations Special Session on Children in 2002 set the elimination of vitamin A deficiency by 2010. The prevalence of night blindness due to vitamin A deficiency is also high among pregnant women in many developing countries. Vitamin A deficiency also contributes to maternal mortalityand other poor outcomes in pregnancy and lactation.[1][2][3][4]

Vitamin A deficiency also diminishes the ability to fight infections. In countries where children are not immunized, infectious disease likemeasles have higher fatality rates. As elucidated by Dr. Alfred Sommer, even mild, subclinical deficiency can also be a problem, as itmay increase children’s risk of developing respiratory and diarrheal infections, decrease growth rate, slow bone development, and decrease likelihood of survival from serious illness.

Alfred (Al) Sommer‘s research on vitamin A in the 1970s and 1980s revealed that dosing severely vitamin A deficient children with an inexpensive, large dose vitamin A capsule twice a year reduces child mortality by as much as 34 percent.[1] The World Bank and, recently, the Copenhagen Consensus list vitamin A supplementation as one of the most cost-effective health interventions in the world.[2][3]

 

Vitamin B deficiency

http://en.wikipedia.org/wiki/B_vitamins#B_vitamin_deficiency

Vitamin Name Deficiency effects
Vitamin B1 thiamine Deficiency causes beriberi. Symptoms of this disease of the nervous system include weight loss, emotional disturbances, Wernicke’s encephalopathy (impaired sensory perception), weakness and pain in the limbs, periods ofirregular heartbeat, and edema (swelling of bodily tissues). Heart failure and death may occur in advanced cases. Chronic thiamine deficiency can also cause Korsakoff’s syndrome, an irreversible psychosis characterized by amnesia and confabulation

 

Vitamin B2 riboflavin Deficiency causes ariboflavinosis. Symptoms may include cheilosis (cracks in the lips), high sensitivity to sunlight, angular cheilitis,glossitis (inflammation of the tongue),seborrheic dermatitis or pseudo-syphilis(particularly affecting the scrotum or labia majora and the mouth), pharyngitis (sore throat), hyperemia, and edema of thepharyngeal and oral mucosa.
Vitamin B3 niacin Deficiency, along with a deficiency oftryptophan causes pellagra. Symptoms include aggression, dermatitisinsomnia,weakness, mental confusion, and diarrhea. In advanced cases, pellagra may lead todementia and death (the 3(+1) Ds: dermatitis, diarrhea, dementia, and death). 

Pellagra is a vitamin deficiency disease most commonly caused by a chronic lack of niacin(vitamin B3) in the diet. It can be caused by decreased intake of niacin or tryptophan[1], and possibly by excessive intake of leucine.[2]It may also result from alterations in protein metabolism in disorders such as carcinoid syndrome. A deficiency of the amino acidlysine can lead to a deficiency of niacin as well, meaning that another potential cause of pellagra is lysine deficiency.[3]

Vitamin B5 pantothenic acid Deficiency can result in acne and paresthesia, although it is uncommon.
Vitamin B6 pyridoxine Deficiency may lead to microcytic anemia(because pyridoxyl phosphate is the cofactor for heme synthesis), depression, dermatitis, high blood pressure (hypertension), water retention, and elevated levels ofhomocysteine.
Vitamin B7 biotin Deficiency does not typically cause symptoms in adults but may lead to impaired growth and neurological disorders in infants. Multiple carboxylase deficiency, an inborn error of metabolism, can lead to biotin deficiency even when dietary biotin intake is normal. 

Initial symptoms of biotin deficiency include:

  1. Dry skin
  2. Seborrheic dermatitis
  3. Fungal infections
  4. Rashes including red, patchy ones near the mouth (erythematous periorofacial macular rash)
  5. Fine and brittle hair
  6. Hair loss or total baldness (alopecia)

If left untreated, neurological symptoms can develop, including:

  1. Mild depression, which may progress to profound lassitude and, eventually, tosomnolence
  2. Changes in mental status
  3. Generalized muscular pains (myalgias)
  4. Hyperesthesias and paresthesias
Vitamin B9 folic acid Deficiency results in a macrocytic anemia, and elevated levels of homocysteine. Deficiency in pregnant women can lead to birth defects. Supplementation is often recommended during pregnancy. Researchers have shown that folic acid might also slow the insidious effects of age on the brain.
Vitamin B12 cobalamin Deficiency results in a macrocytic anemia, elevated homocysteineperipheral neuropathy, memory loss and other cognitive deficits. It is most likely to occur among elderly people, as absorption through the gut declines with age; the autoimmune disease pernicious anemia is another common cause. It can also cause symptoms of mania and psychosis. In rare extreme cases, paralysis can result. 

 

Vitamin B12 deficiency is a reduction invitamin B12 from inadequate dietary intake or impaired absorption. The condition is commonly asymptomatic, but can also present as anemia characterized by enlarged blood corpuscles with characteristic changes in neutrophils, known as megaloblastic anemia.

In serious cases deficiency can potentially cause severe and irreversible damage to the nervous system, including subacute combined degeneration of spinal cord.

The anemia is thought to be due to problems in DNA synthesis, specifically in the synthesis of thymine, which is dependent on products of the MTR reaction. Other blood cell types such as white blood cells and platelets are often also low. Bone marrow examination may showmegaloblastic hemopoiesisThe anemia responds completely to vitamin B12; theneurological symptoms (if any) respond partly or completely, depending on prior severity and duration.

 


 

Vitamin C deficiency

Symptoms and Signs of Vitamin C Deficiency

It takes several months of low amounts of vitamin C to lead to the symptoms of scurvy. The classic symptoms are bleeding gums, scaly skin, loose teeth, fatigue, increased risk of infection, and poor wound healing. Children and infants with an ascorbic acid deficiency usually have poor bone growth and anemia.

http://www4.dr-rath-foundation.org/NHC/cardiovascular_disease/lecture/stanford_speech.htm

This animation (requires RealVideoPlayer) shows the connection between cardiovascular disease and the sailor’s disease scurvy. As opposed to animals, the human body cannot synthesize vitamin C. Ascorbate deficiency results in two distinct morphological changes of the vascular wall: Impaired vascular stability due to decreased collagen synthesis and loss of the endothelial barrier function.
The sailors of earlier centuries died within a few months from hemorrhagic blood loss due to lack of endogenous ascorbate synthesis combined with a vitamin deficient diet aboard. When the Indians gave those sailors tea from tree barks and other vitamin rich nutrition, blood loss was stopped and the vascular wall healed naturally.Today, everyone gets some vitamin C and open scurvy is rare. But almost everyone suffers from chronic vitamin deficiency. Over decades, micro lesions develop in the vascular wall, especially in areas of high mechanical stress such as the coronary arteries.

Vitamin E deficiency

http://en.wikipedia.org/wiki/Vitamin_E_deficiency

Vitamin E deficiency causes neurological problems due to poor nerve conduction. These include neuromuscular problems such as spinocerebellar ataxia andmyopathies.[1] Deficiency can also cause anemia, due to oxidative damage to red blood cells.

Vitamin E deficiency is rare in humans and is almost never caused by a poor diet.[1]Instead, there are three specific situations when a vitamin E deficiency is likely to occur. It is seen in persons who cannot absorb dietary fat, has been found in premature, very low birth weight infants (birth weights less than 1500 grams, or 3.5 pounds), and is seen in individuals with rare disorders of fat metabolism.[2]

Individuals who cannot absorb fat may require a vitamin E supplement because some dietary fat is needed for the absorption of vitamin E from the gastrointestinal tract. Anyone diagnosed with cystic fibrosis, individuals who have had part or all of their stomach removed, and individuals with malabsorptive problems such as Crohn’s diseaseliver disease or pancreatic insufficiency may not absorb fat and should discuss the need for supplemental vitamin E with their physician. People who cannot absorb fat often pass greasy stools or have chronic diarrhea and bloating.

Very low birth weight infants may be deficient in vitamin E. A neonatologist, apediatrician specializing in the care of newborns, typically evaluates the nutritional needs of premature infants.

Abetalipoproteinemia is a rare inherited disorder of fat metabolism that results in poor absorption of dietary fat and vitamin E.[3] The vitamin E deficiency associated with this disease causes problems such as poor transmission of nerve impulses, muscle weakness, and degeneration of the retina that can cause blindness.Individuals with abetalipoproteinemia may be prescribed special vitamin E supplements by a physician to treat this disorder. In addition, there is a rare genetic condition termed isolated vitamin E deficiency or ataxia with isolated with vitamin E deficiency, caused by mutations in the gene for the tocopherol transfer protein.[4] These individuals have an extremely poor capacity to absorb vitamin E and develop neurological complications that are reversed by high doses of vitamin E.

 

Vitamin K deficiency

http://en.wikipedia.org/wiki/Vitamin_K

Vitamin K is a group of lipophilichydrophobic vitaminsthat are needed for the posttranslational modification of certain proteins, mostly required for blood coagulation but also involved in metabolism pathways in bone and other tissue.

 

Symptoms of Vitamin K DeficienciesVitamin K is known to be needed to coagulate blood and to maintain proper bone density. It plays a key role in proper development of the fetus. Deficiencies of vitamin K have been linked to:

Heavy menstrual bleeding*
Gastrointestinal bleeding
Hematuria (blood in the urine)
Nosebleeds
Eye hemorrhages
Anemia
Gum bleeding
Prolonged clotting times
Hematomas
Hemorrhaging
Ovarian Hemorrhaging
Easy bruising
Purpura
Osteopenia
Osteoporosis
Fractures
Hypercalciuria
Liver Cancer
Calcification of soft tissue, especially heart valves (See my section on Calcium Deposits for more on this topic).
Birth defects linked directly to vitamin K deficiencies include:

Underdevelopment of the nose, mouth and mid face
Shortened fingers
Cupped ears
Flat nasal bridges

The following birth defects have been linked to anticonvulsant drugs, which block vitamin K:

Epicanthal folds
Flat nasal bridge
Short noses
Variety of craniofacial abnormalities
Neural tube defects
Mental retardation
Learning disabilities
Long, thin overlapping fingers
Hypertelorism
Upslanting palpebral fissures
Microcephaly
Cardiac abnormalities
Distal digit hypoplasia (shortened pinkie fingers)
Growth deficiency

 

Iron deficiency

http://en.wikipedia.org/wiki/Iron_deficiency_(medicine)

 

Iron deficiency (sideropenia or hypoferremia) is one of the most commonly known forms of nutritional deficiencies. In the human bodyiron is present in all cellsand has several vital functions—as a carrier of oxygen to the tissues from the lungs in the form of hemoglobin, as a transport medium for electrons within the cells in the form of cytochromes, and as an integral part of enzymereactions in various tissues. Too little iron can interfere with these vital functions and lead to morbidity anddeath.

The direct consequence of iron deficiency is iron deficiency anemia. Groups that are most prone to developing this disease are children and pre-menopausal women.

 

 

Boron deficiency

http://en.wikipedia.org/wiki/Boron_deficiency_(medicine)

Boron deficiency is a pathology which may occur inanimals due to a lack of boron. A report given by E. Wayne Johnson et al. at the 2005 Alan D. Leman Swine Conference[1] suggests that boron deficiency producesosteochondrosis in swine that is correctable by addition of 50 ppm of boron to the diet. The amount of boron required by animals and humans is not yet well established.

According to some natural therapy researchers,[2] topsoilused over long periods of time for agriculture become boron-deficient to some extent, and humans eating produce from boron-rich soils have reduced incidence ofarthritis and osteoporosis.

 

http://findarticles.com/p/articles/mi_m0FDN/is_4_9/ai_n9479460/

Deficiency States

Information on boron deficiency in humans is minimal; however, it appears a deficiency in boron impacts mineral metabolism, cognitive function, steroid hormone and vitamin levels, and bone integrity. (20) Boron-deficient diets have resulted in embryological defects in some but not all animals (e.g., not in rodents), pointing to a possible role in reproduction and/or development. Limited growthis also commonly noted in boron-depleted animals, (17,21) while boron-deficient chicks present increased insulin secretion. (19,22)

Clinical Applications Anemia

Boron supplementation to subjects who had previously followed a dietary regimen deficient in boron resulted in increases in blood hemoglobin concentrations, mean corpuscular hemoglobin, and mean corpuscular hemoglobin concentration, and decreases in hematocrit, red cell count and platelet count. (23)

Osteo- and Rheumatoid Arthritis

In a double-blind, placebo-controlled trial of 20 subjects with osteoarthritis, half of the subjects receiving a daily supplement containing 6 mg boron noted subjective improvement in their condition. (24)

Clinical commentary suggests children with juvenile arthritis (Still’s disease) improve with boron supplementation (6-9 mg daily). (25)

Individuals with rheumatoid arthritis might experience an aggravation of symptoms (Herxheimer response) for 1-3 weeks, but generally notice improvement within four weeks of beginning boron supplementation (6-9 mg daily). (25)

Cognitive Function

Collectively, data indicate that boron might play a role in human brain function, alertness, and cognitive performance. In humans, low boron intake compared to high boron intake was associated with poor short- and long-term memory, eye-hand coordination, and manual dexterity. (26) Boron deficiency has also been associated with decreased brain electrical activity similar to brainwave patterns observed in nonspecific malnutrition. (27)

 

Selenium Deficiency

http://www.suite101.com/content/selenium-deficiency-a10750

Selenium deficiency is thought to contribute toautoimmune disease by making the body more susceptible to nutritional and biochemical stresses as well as infectious diseases. Three diseases caused directly by selenium deficiency include Keshan Disease, which causes an enlarged heart, Kashin-Beck Disease, which causes osteoarthropathy, and Myxedematous Endemic Cretinism, a form of hypothyroidism which results in mental retardation.

  • Fatigue
  • Miscarriage
  • Hyperthyroidism
  • Lack of mental dexterity

However, there are diseases that can be caused by this deficiency as well and they include Keshan disease and Kashin-Beck disease.

Keshan disease is viral disease and mostly affects children. It is caused by a deficient amount of selenium present in the body. The main symptom of this condition is myocardial necrosis, which leads to the weakening of the heart and a general weakness of the heart muscle. Keshan disease can also make a personmuch more susceptible to developing other illnesses.

Kashin-Beck disease occurs when the body is deficient of both selenium and iodine. The symptoms this can then present include the degeneration of cartilage.

So, what exactly causes a selenium deficiency in the first place? Eating food that is grown in soil lacking this nutrient is thought to be the primary cause. Also, people suffering from intestinal disorders that make the absorption of selenium next to impossible are at an elevated risk for developing this deficiency.

Treatment usually consists of taking selenium supplements until the body’s levels have returned to normal. However, supplements may always be necessary if absorption is a problem.

 

Melatonin deficiency

http://www.prevention.com/cda/vendorarticle/melatonin/HN2883002/health/vitamin.encyclopedia/0/0/symptoms.of.deficiency

Adults with insomnia have been shown to have lower melatonin levels.4 Frequent travelers and shift workers are also likely to benefit from melatonin for the resynchronization of their sleep schedules,5 though a melatonin “deficiency” as such does not exist for these people. Patients with heart disease have been reported to have low melatonin levels, but whether this abnormality increases the risk of heart disease or whether heart disease leads to the low melatonin level is not yet known.6 People with schizophrenia were found to have low melatonin output and experienced significantly improved sleep following melatonin replacement supplementation.7

http://www.restorativemedicine.com/books/fundamentals-of-naturopathic-endocrinology/professionals/pineal-disorders/melatonin-deficiency-and-excess

Adeficient production of melatonin can result in anxiety and mood disorders, lowered basal body temperature insomnia, elevated estrogen/progesterone ratio, and immune suppression associated with cancer.

 

Magnesium deficiency

http://www.ctds.info/5_13_magnesium.html

The diets of all Americans are likely to be deficient……..Even a mild deficiency causes sensitiveness to noise, nervousness, irritability, mental depression, confusion, twitching, trembling, apprehension, insomnia, muscle weakness and cramps in the toes, feet, legs, or fingers.

Magnesium (Mg) is a trace mineral that is known to be required for several hundred different functions in the body. A significant portion of the symptoms of many chronic disorders are identical to symptoms of magnesium deficiency. Studies show many people in the U.S. today do not consume the daily recommended amounts of Mg. A lack of this important nutrient may be a major factor in many common health problems in industrialized countries. Common conditions such as mitral valve prolapse, migraines, attention deficit disorder, fibromyalgia, asthma and allergies have all been linked to a Mg deficiency. Perhaps not coincidentally, these conditions also tend to occur in clusters together within the same individual. A magnesium deficiency as a root cause would provide a logical explanation of why some people suffer from a constellation of these types of problems.Many of the following conditions commonly occur in conjunction with each other and all have been linked to a Mg deficiency.

Contents:

  • Allergies, Chemical Sensitivities
  • Anxiety and Psychiatric Disorders
  • Aorta Strength
  • Asthma
  • Attention Deficit Disorder
  • Calcification of Soft Tissue Including Heart Valve
  • Diabetes
  • Also see:
    Magnesium – Part Two - Covers the links between magnesium deficiency and diverse conditions such asfibromyalgia, hearing loss, migraines, menstrual cramps (dysmenorrhea), mitral valve prolapse, muscle cramps, nystagmus, osteoporosis, pectus excavatum, TMJ and more.
What is the percentage of Americans with inadequate intakes of Mg from food based on estimated average requirements?56%

 

 

Calcium deficiency

http://www.wrongdiagnosis.com/c/calcium_deficiency/symptoms.htm#symptom_list

Calcium is the most abundant mineral found in the human body. The majority (99%) is stored in the bones and teeth; the rest is stored in muscle tissue and blood. In addition to bone building and remodeling, calcium is also responsible for muscle contraction, central nervous function and hormone secretion. Calcium deficiency is of major concern in the United States. An estimated 44-87% of Americans don’t get enough

Symptoms of Calcium deficiency

The list of signs and symptoms mentioned in various sources forCalcium deficiency includes the 23 symptoms listed below:

 

Symptoms of Hypocalcaemia

http://en.wikipedia.org/wiki/Hypocalcaemia#Symptoms

Petechia which appear as one-off spots, then later become rashes.

The Food and Drug Administration on Tuesday announced a gradual but potentially far-reaching effort to reduce the amount of salt Americans consume in a bid to combat high blood pressure, heart disease, strokes and other health problems that have soared to near-epidemic proportions.

 

Based on what evidence?

http://www.saltinstitute.org/Issues-in-focus/Food-salt-health/Salt-and-cardiovascular-health

1985. A ten-year study of nearly 8,000 Hawaiian Japanese men concluded: “No relation was found between salt intake and the incidence of stroke.”

1995. An eight-year study of a New York City hypertensive population stratified for sodium intake levels found those on low-salt diets had more than four times as many heart attacks as those on normal-sodium diets – the exact opposite of what the “salt hypothesis” would have predicted.

1997. An analysis by NHLBI’s Dr. Cutler of the first six years’ data from the MRFIT database documented no health outcomes benefits of lower-sodium diets.

1997. A ten-year follow-up study to the huge Scottish Heart Health Study found no improved health outcomes for those on low-salt diets.

1998. An analysis of the health outcomes over twenty years from those in the massive US National Health and Nutrition Examination Survey (NHANES I) documented a 20% greater incidence of heart attacks among those on low-salt diets compared to normal-salt diets

1998. A health outcomes study in Finland, reported to the American Heart Association that no health benefits could be identified and concluded “…our results do not support the recommendations for entire populations to reduce dietary sodium intake to prevent coronary heart disease.”

1999. A further analysis of the MRFIT database, this time using fourteen years’ data, confirmed no improved health benefit from low-sodium diets. Its author conceded that there is “no relationship observed between dietary sodium and mortality.”

1999. A study of Americans found that less sodium-dense diets did reduce the cardiovascular mortality of one population sub-set, overweight men – the article reporting the findings did not explain why this obese group actually consumed less sodium than normal-weight individuals in the study.

2001. A Finnish study reported an increase in cardiovascular events for obese men (but not women or normal-weight individuals of either gender) – the article, however, failed to adjust for potassium intake levels which many researchers consider a key associated variable.

2002. In September, 2002, the prestigious Cochrane Collaboration produced the latest and highest-quality meta-analysis of clinical trials. It was published in the British Medical Journal and confirmed earlier meta-analyses’ conclusions that significant salt reduction would lead to very small blood pressure changes in sensitive populations and no health benefits.

2003. In June 2003, Dutch researchers using a massive database in Rotterdam concluded that “variations in dietary sodium and potassium within the range commonly observed in Westernized societies have no material effect on the occurrence of cardiovascular events and mortality at old age.”

2004. In July 2004, the first “outcomes” study identifying a population risk appeared in Stroke magazine. Researchers found that in a Japanese population, “low” sodium intakes (about 20% above Americans’ average intake) had one-third the incidence of fatal strokes of those consuming twice as much sodium as Americans.

2006. A March 2006 analysis of the federal NHANES II database in The American Journal of Medicine found a 37% higher cardiovascular mortality rate for low-sodium dieters

2007. A February 2007 reported in the International Journal of Epidemiology studied 40,547 Japanese over seven years and found “the Japanese dietary pattern was associated with a decreased risk of CVD mortality, despite its relation to sodium intake and hypertension.”

2007. An April 2007 article in the British Medical Journal found a 25% lower risk of CV events in a group which years earlier had achieved significant sodium reduction during two clinical trials (TOHP I and TOHP II).

2007. An October 2007 analysis of a large Dutch database published in the European Journal of Epidemiology documented no benefit of low-salt diets in reducing stroke or heart attack incidence nor lowering death rates.

2008. A May 2008 examination of NHANES II (the largest US federal database of nutrition and health) published in the Journal of General Internal Medicine confirmed two earlier studies of earlier NHANES surveys that there is no health benefit (CVD or all-cause mortality) for those on low-sodium diets.

 

Salt deficiencyhttp://www.shirleys-wellness-cafe.com/salt.htm

Both sea salt and rock salt were well known to the ancient Greeks who noted that eating salty food affected basic body functions such as digestion and excretion (urine and stools). This led to salt being used medically. The healing methods of Hippocrates (460 BC) especially made frequent use of salt. Hippocrates mentions inhalation of steam from salt-water. We know today that the antiinflammatory effects of inhaled salt provide relief from respiratory symptoms (c). Thus, 2000 years ago, Greek medicine had already discovered topical use of salt for skin lesions, drinking salty or mineralized waters for digestive troubles and inhaling salt for respiratory diseases.

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Supreme Court rules against ban on GMO alfalfa, but requires complete safety study first

Posted on 08 August 2010 by admin

(NaturalNews) The battle continues as agri-giant Monsanto pushes to have its genetically-modified (GM) alfalfa approved for use in the U.S. Recently, the U.S. Supreme Court sided with Monsanto by ruling against a lower court’s nationwide ban on the GM alfalfa; however, the court is requiring the U.S. Department of Agriculture (USDA) to complete a comprehensive safety study before the “franken-crop” can officially be approved.

The whole thing started when the USDA first approved Monsanto’s GM alfalfa back in 2007. The Center for Food Safety (CFS) immediately filed a lawsuit against the approval, citing valid concerns that the seeds would take over pasture lands and become uncontrollable. The federal district judge who heard the case agreed, ruling also that the USDA had acted irresponsibly by failing to complete an environmental safety study prior to approving the seeds for planting. The same judge banned GM alfalfa nationwide.

The reason why GM alfalfa is particularly dangerous is that alfalfa is an aggressive spreader, and would likely end up in all sorts of fields, including organic ones. Alfalfa is typically used to feed dairy cattle, so if GM alfalfa is ever approved, it could destroy the entire organic beef and dairy industry. In the long term, it could ruin the entire organic food industry.

However, the Supreme Court recently ruled 7-to-1 that a nationwide ban was inappropriate, but it has allowed the ban to stay in place until the USDA completes the necessary Environmental Impact Statement (EIS).

According to the Alliance for Natural Health (ANH), Monsanto was quick to spin the ruling as being in its favor, essentially telling the media that it had won a victory. But truth be told, the nationwide ban on GM alfalfa is still in place, and planting the crop is still illegal. Though the ruling allows Monsanto to move forward in trying to gain approval, there is no guarantee that the multi-national giant will be successful.

Part of the EIS process involves reviewing the more than 200,000 public comments received since December 2009 concerning GM alfalfa, most of which are likely in protest of the crop.

So it is important to keep letting your voice be heard on important issues like this one, especially when there is an open comment period. 200,000 people voiced their opinions about GM alfalfa, and this could greatly influence the USDA’s final decision in the matter.

Sources:

Supreme Court Kicks Critical Genetically Modified Alfalfa Issue Down The Road – Alliance for Natural Health

Genetically Modified Foods: More Reason to Avoid Them; Why They Threaten Organic Agriculture

Dangers of Genetically Engineered Foods – Institute for Responsible Technology

Learn more:http://www.naturalnews.com/029407_GMOs_alfalfa.html#ixzz1auqqYWiL

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