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California Police raid Organic Food store GUNS DRAWN looking for raw milk!!

Posted on 06 August 2010 by admin

Food police target organic foods in California! on TV News

http://www.youtube.com/watch?v=ifvp3Fxi7Uo
Police raided the Rawsome Foods organic grocery store with guns drawn in search of “raw-foods”. George Hemminger (George4Title) said the battle over organic foods is heating up because large agricultural businesses and corporations feel threatened by local co-ops and have hijacked the FDA and other government regulatory agencies.

RAW VIDEO: California Police raid Organic Food store GUNS DRAWN looking for raw milk!!


http://www.youtube.com/watch?v=MHoFY7h-do8
California Police raid organic food store looking for raw milk!!

Keep Raw Milk LEGAL!!


http://www.youtube.com/watch?v=56tiOnGSgyQ
In October 2007, California State Legislature passed a bill banning the sale of raw milk. Despite its medicinal value, raw milk will no longer be available to the public. Republican Presidential Candidate Dr. Ron Paul has introduced a bill to legalize the transportation of unpasteurized milk. Please help save raw milk. Visit www.organicpastures.com to make a donation.

H. R. 778 Unpasteurized (Raw) Milk Legalization Bill

To authorize the interstate traffic of unpasteurized milk and milk products that are packaged for direct human consumption.

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USDA Announces and Seeks COMMENTS on Standard-Setting Activities of the Codex Alimentarius Commission

Posted on 01 July 2010 by admin

USDA Announces and Seeks Comments on Standard-Setting Activities of the Codex Alimentarius Commission
Congressional and Public Affairs
(202) 720-9113
Catherine Cochran

WASHINGTON, July 1, 2010 - The U.S. Department of Agriculture’s Office of Food Safety (OFS) today is inviting comments on standard-setting activities of the Codex Alimentarius Commission (Codex). Codex activities announced include phytosanitary standard-setting activities, commodity standards, guidelines, codes of practice, and revised texts.

In a Federal Register Notice published on June 4, 2010, OFS describes the standard setting activities for the Codex Commission and for each of the Committiees. For more information, go towww.fsis.usda.gov/Frame/FrameRedirect.asp?main=http://www.fsis.usda.gov/OPPDE/rdad/FRPubs/2009-0033.htm. Documents pertaining to Codex standard setting activities are accessible online atwww.codexalimentarius.net/current.asp. OFS seeks comments on standards under consideration and recommendations for new standards for the time period between June 1, 2010 to May 31, 2011.

Comments may be submitted through the Federal eRulemaking Portal at www.regulations.gov, or by mail to Docket Clerk, U.S. Department of Agriculture, Food Safety and Inspection Service, Room 2-2127, George Washington Carver Center, 5601 Sunnyside Ave., Beltsville, MD 20705, Mailstop 5272. All items submitted by mail or e-mail must include the Agency name and docket number FSIS-2009-0033. Comments received in response to the docket will be made available for public inspection and posted without change, including personal information, towww.regulations.gov.

Codex was established in 1963 by two United Nations organizations, the Food and Agriculture Organization (FAO) and the World Health Organization (WHO). Through adoption of food standards, codes of practice and other guidelines developed by its committees, and by promoting their adoption and implementation by governments, Codex seeks to protect the health of consumers and ensure fair practices in the food trade.

For further information, contact Karen Stuck, United States Manager for Codex, by mail at U.S. Department of Agriculture, Office of Food Safety, Room 4861, South Agriculture Building, 1400 Independence Ave. SW, Washington, DC 20250. Karen Stuck can also be reached by phone at (202) 205-7760, by fax at (202) 720-3157, or by e-mail at USCodex@fsis.usda.gov.

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Last Modified: July 1, 2010

http://www.fsis.usda.gov/News_&_Events/NR_070110_01/index.asp

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Obama Implements Codex Alimentarius Council by Executive Order

Posted on 18 June 2010 by admin

The White House, Office of the Press Secretary

For Immediate Release
June 10, 2010

Executive Order– Establishing the National Prevention, Health Promotion, and Public Health Council

EXECUTIVE ORDER

ESTABLISHING THE NATIONAL PREVENTION, HEALTH PROMOTION, AND PUBLIC HEALTH COUNCIL

By the authority vested in me as President by the Constitution and the laws of the United States of America, including section 4001 of the Patient Protection and Affordable Care Act (Public Law 111-148), it is hereby ordered as follows:

Section 1. Establishment. There is established within the Department of Health and Human Services, the National Prevention, Health Promotion, and Public Health Council (Council).

Sec. 2. Membership.

(a) The Surgeon General shall serve as the Chair of the Council, which shall be composed of:

(1) the Secretary of Agriculture;
(2) the Secretary of Labor;
(3) the Secretary of Health and Human Services;
(4) the Secretary of Transportation;
(5) the Secretary of Education;
(6) the Secretary of Homeland Security;
(7) the Administrator of the Environmental Protection Agency;
(8) the Chair of the Federal Trade Commission;
(9) the Director of National Drug Control Policy;
(10) the Assistant to the President and Director of the Domestic Policy Council;
(11) the Assistant Secretary of the Interior for Indian Affairs;
(12) the Chairman of the Corporation for National and Community Service; and
(13) the head of any other executive department or agency that the Chair may, from time to time, determine is appropriate.

(b) The Council shall meet at the call of the Chair.

Sec. 3. Purposes and Duties. The Council shall:

(a) provide coordination and leadership at the Federal level, and among all executive departments and agencies, with respect to prevention, wellness, and health promotion practices, the public health system, and integrative health care in the United States;

(b) develop, after obtaining input from relevant stakeholders, a national prevention, health promotion, public health, and integrative health-care strategy that incorporates the most effective and achievable means of improving the health status of Americans and reducing the incidence of preventable illness and disability in the United States, as further described in section 5 of this order;

(c) provide recommendations to the President and the Congress concerning the most pressing health issues confronting the United States and changes in Federal policy to achieve national wellness, health promotion, and public health goals, including the reduction of tobacco use, sedentary behavior, and poor nutrition;

(d) consider and propose evidence-based models, policies, and innovative approaches for the promotion of transformative models of prevention, integrative health, and public health on individual and community levels across the United States;

(e) establish processes for continual public input, including input from State, regional, and local leadership communities and other relevant stakeholders, including Indian tribes and tribal organizations;

(f) submit the reports required by section 6 of this order; and

(g) carry out such other activities as are determined appropriate by the President.

Sec. 4. Advisory Group.

(a) There is established within the Department of Health and Human Services an Advisory Group on Prevention, Health Promotion, and Integrative and Public Health (Advisory Group), which shall report to the Chair of the Council.

(b) The Advisory Group shall be composed of not more than 25 members or representatives from outside the Federal Government appointed by the President and shall include a diverse group of licensed health professionals, including integrative health practitioners who are representative of or have expertise in:

(1) worksite health promotion;
(2) community services, including community health centers;
(3) preventive medicine;
(4) health coaching;
(5) public health education;
(6) geriatrics; and
(7) rehabilitation medicine.

(c) The Advisory Group shall develop policy and program recommendations and advise the Council on lifestyle-based chronic disease prevention and management, integrative health care practices, and health promotion.

Sec. 5. National Prevention and Health Promotion Strategy. Not later than March 23, 2011, the Chair, in consultation with the Council, shall develop and make public a national prevention, health promotion, and public health strategy (national strategy), and shall review and revise it periodically. The national strategy shall:

(a) set specific goals and objectives for improving the health of the United States through federally supported prevention, health promotion, and public health programs, consistent with ongoing goal setting efforts conducted by specific agencies;

(b) establish specific and measurable actions and timelines to carry out the strategy, and determine accountability for meeting those timelines, within and across Federal departments and agencies; and

(c) make recommendations to improve Federal efforts relating to prevention, health promotion, public health, and integrative health-care practices to ensure that Federal efforts are consistent with available standards and evidence.

Sec. 6. Reports. Not later than July 1, 2010, and annually thereafter until January 1, 2015, the Council shall submit to the President and the relevant committees of the Congress, a report that:

(a) describes the activities and efforts on prevention, health promotion, and public health and activities to develop the national strategy conducted by the Council during the period for which the report is prepared;

(b) describes the national progress in meeting specific prevention, health promotion, and public health goals defined in the national strategy and further describes corrective actions recommended by the Council and actions taken by relevant agencies and organizations to meet these goals;

(c) contains a list of national priorities on health promotion and disease prevention to address lifestyle behavior modification (including smoking cessation, proper nutrition, appropriate exercise, mental health, behavioral health, substance-use disorder, and domestic violence screenings) and the prevention measures for the five leading disease killers in the United States;

(d) contains specific science-based initiatives to achieve the measurable goals of the Healthy People 2020 program of the Department of Health and Human Services regarding nutrition, exercise, and smoking cessation, and targeting the five leading disease killers in the United States;

(e) contains specific plans for consolidating Federal health programs and centers that exist to promote healthy behavior and reduce disease risk (including eliminating programs and offices determined to be ineffective in meeting the priority goals of the Healthy People 2020 program of the Department of Health and Human Services);

(f) contains specific plans to ensure that all Federal health-care programs are fully coordinated with science-based prevention recommendations by the Director of the Centers for Disease Control and Prevention; and

(g) contains specific plans to ensure that all prevention programs outside the Department of Health and Human Services are based on the science-based guidelines developed by the Centers for Disease Control and Prevention under subsection (d) of this section.

Sec. 7. Administration.

(a) The Department of Health and Human Services shall provide funding and administrative support for the Council and the Advisory Group to the extent permitted by law and within existing appropriations.

(b) All executive departments and agencies shall provide information and assistance to the Council as the Chair may request for purposes of carrying out the Council’s functions, to the extent permitted by law.

(c) Members of the Advisory Group shall serve without compensation, but shall be allowed travel expenses, including per diem in lieu of subsistence, as authorized by law for persons serving intermittently in Government service (5 U.S.C. 5701-5707), consistent with the availability of funds.

Sec. 8. General Provisions.

(a) Insofar as the Federal Advisory Committee Act, as amended (5 U.S.C App.) may apply to the Advisory Group, any functions of the President under that Act, except that of reporting to the Congress, shall be performed by the Secretary of Health and Human Services in accordance with the guidelines that have been issued by the Administrator of General Services.

(b) Nothing in this order shall be construed to impair or otherwise affect:

(1) authority granted by law to an executive department, agency, or the head thereof; or
(2) functions of the Director of the Office of Management and Budget relating to budgetary, administrative, or legislative proposals.

(c) This order is not intended to, and does not, create any right or benefit, substantive or procedural, enforceable at law or in equity by any party against the United States, its departments, agencies, or entities, its officers, employees, or agents, or any other person.

BARACK OBAMA

THE WHITE HOUSE,
June 10, 2010

Source: Barack Obama, White House

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Food Illuminati, GMO Labeling and Codex Alimentarius

Posted on 09 June 2010 by admin

codex2.jpg
Codex Alimentarius
Page 1 of 108 of a Codex publication


What is the Codex? More Michael Pollan and less Dan Brown–we hope. The little-known Codex Alimentarius Commission (CAC) was established in 1963 under the joint auspices of the United Nations and the World Health Organization to devise universal guidelines pertaining to food production, safety and marketing. Its resolutions are not binding; rather, member countries use them as frameworks for local legislation and regulation. Codex texts are exhaustive, technical and occasionally compelling, particularly if you happen to be interested in standards for whole and decorticated pearl millet grains. All texts are publicly available in PDF format at the Codex website.

 

It’s no surprise that an organization operating largely beyond public scrutiny for almost 50 years to define what we know about what we eat has attracted the fulsome indictments of the lunatic fringe. In fact, the Commission has a set of FAQs to explicitly debunk some of the more egregious rumors about their practices and intent.

This doesn’t mean the Codex is above malignant influence. At a recent meeting of the Codex Committee on Food Labeling in Quebec City, Canada, U.S. representatives lobbied the Committee to adopt language specifying that “GM/GE [Genetically Modified/ Genetically Engineered] foods are [not] in any way different from other foods” and went so far as to suggest that mandatory GMO labeling elsewhere in the world could confuse the consumer and should be prohibited.

That the United States insisted that labeling criteria in other countries could be misleading, despite the fact that voluntary GMO notification is permitted within its own borders, constituted a stunning overreach that alarmed consumer and food safety watchdogs across the country. A broad coalition of more than 80 agricultural groups, policy wonks, farmers’ collectives and food activists–among them familiar names like Lundberg Family Farms, theCenter for Media and Democracy and Ithaca, New York’s famed Moosewood Restaurant–submitted a letter to FDA and USDA reps decrying the draft policy:

The current draft US Codex position [says] that mandatory labeling of food as GE/GM ‘is likely to create the impression that the labeled food is in some way different’ and would therefore be ‘false, misleading or deceptive.’ [...] We find it hard to understand how FDA and USDA can argue to Codex that mandatory labeling is inherently false and misleading, but voluntary labeling, which is permitted in the United States, is not. We are, in fact, concerned that the current US position appears to seek to establish precedents at Codex that would make it difficult to label food as non-GM in the US.

 

As the Monsantos and Cargills of the world continue to parry demands for mandatory GM labeling and rebuff notions that GM products are problematic to human and environmental health, you would be excused for suspecting the FDA and USDA were lobbying on behalf of agribusiness, rather than the public whom they where chartered to protect. The 64th session of the Executive Committee of the Codex Alimentarius will be called to order in Geneva, Switzerland on June 29th. Labeling standards proposed for adoption appear on the official agenda.

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USDA DEREGULATES GM Soybean, DuPont and Monsanto begin Cooking-Oil War

Posted on 07 June 2010 by admin

The Agriculture Department will approve for broad use tomorrow a genetically modified soybean engineered to contain healthier oils, the opening salvo in a biotech oil fight between DuPont Co. and its rival, Monsanto Co.

The high-oleic soybean, developed by DuPont and pending deregulation since 2006, is one of the first in a wave of bioengineered cash crops that are being altered for nutritional purposes. Currently, nearly all biotech crops grown in the United States have been altered for resistance to weedkiller or insects, traits that are rarely felt by consumers or commercial businesses.

The USDA deregulation is the “final step” in the approval process for Dupont’s soybean, which has already been approved in Canada and Mexico, said Bridget Anderson, a spokeswoman for Pioneer Hi-Bred, DuPont’s biotech seed business. The crop and its oil will continue commercial testing this year and should be ready for global use by 2012, she added.

The USDA approval is also the first play in a coming oil war between DuPont and Monsanto.

Currently, Monsanto has two varieties of biotech soybeans pending approval with USDA that also seek to modify the nutritional value of soybean oil, promising to eliminate trans fats and produce oil with omega-3 fatty acid — fish oil — for use in yogurt, granola bars and spreads.

The modified soybeans represent a move by DuPont and Monsanto to broaden the crop traits engineered in their seeds beyond simple properties like pest resistance to complex areas — like nutritional value, drought tolerance and nitrogen fixation — that are often influenced by multiple genes. These long-promised traits previously found little purchase in the seed giant’s business plans.

It is “pretty exciting science,” said Rob Fraley, Monsanto’s chief technology officer. Leveraging improvements in breeding and biotechnology, he said, seed giants like Monsanto “can start to take on some of the most complex physiological traits in terms of crop quality and health and nutrition.”

DuPont’s biotech soybean could be welcome news for soy farmers, who have seen food companies move away from standard soybean oil as they work to eliminate trans fats, which are linked to coronary health risks, from their ingredients. It is a difficult shift. The industry uses about 6 billion pounds of the oil each year, all of which contained trans fats.

The biotech soy will provide a stable oil alternative that can be used without hydrogenation, the process that creates trans fats, DuPont said. The oil has already been tested successfully for snack food preparation for frying or spraying, according to DuPont.

Notably, the engineered soybeans have been created through a different process than most biotech crops on the market, which contain splices of bacterial genes to grant herbicide or pest resistance. Instead, DuPont scientists “silenced” the expression of a gene in the fatty acid pathways of the soybean seeds. Few commercial biotech crops have used gene silencing so far, with a virus-resistant papaya in Hawaii being a notable exception.

Widespread adoption of DuPont or Monsanto’s next-generation soybeans, which would also include traits for weedkiller or pest resistance, would be unlikely to shift the soy crop further toward bioengineering, simply because there is little room for expansion: More than 90 percent of the U.S. soybean crop is already genetically engineered.

Products produced with DuPont’s high-oleic soybeans are unlikely to hit the market until 2012 at the latest, as the company awaits import approval for the crops from the European Union and other important exports markets, the company said.

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Obama’s USDA to deceive Americans over GMO crops

Posted on 02 June 2010 by admin

(NaturalNews) The Obama administration’s Department of Agriculture (USDA) is attempting to downplay the risks of genetically modified alfalfa, a crop previously banned by numerous federal courts.

In 2007, a federal court rejected the Bush USDA’s approval of alfalfa plants genetically engineered for resistance to the Monsanto herbicide Roundup. The court ruled that the USDA had not properly considered the risks posed by the crop. These risks included the possibility that the genetically modified (GM) crops could swap genetic material with related species, thus contaminating neighboring fields or producing non-agricultural “super weeds.”

Monsanto continues to appeal the decision, even though the Ninth Circuit Court of Appeals has ruled against it twice. The case is now pending consideration by the Supreme Court.

Alfalfa is the first perennial crop to be genetically modified. Because it does not die after a year but can regenerate itself from even its roots, the risk of genetic contamination is higher than even that from GM annual crops, which have already been documented to spread beyond the fields they are planted in.

“Widespread [GM] contamination of organic alfalfa is inevitable if the Obama Administration successfully distorts science and ignores public opinion and allows Monsanto’s GM Roundup Ready alfalfa to be planted across the U.S.,” said Ronnie Cummins of the Organic Consumers Association.

After Obama appointed former Monsanto executive Tom Vilsack to head the USDA, the agency released a new draft environmental impact statement (EIS) that continues to play down these risks.

Yet even the Monsanto-friendly EIS acknowledges that “acute toxicity … was observed” in mice that consumed GM alfalfa. It also admits that residues of Roundup (glyphosate) herbicide are toxic.

“Based on upper estimates of exposure… infants consuming fruit and all age groups consuming vegetables may be at risk of adverse effects associated with acute exposure to glyphosate residues,” the statement reads.

Since the introduction of Roundup Ready GM crops 13 years ago, herbicide use has increased by 383 million pounds.

Sources for this story include: www.huffingtonpost.com/ronnie-cummi….

Learn more: http://www.naturalnews.com/028911_USDA_GM_crops.html#ixzz1auSCnGw1

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USDA Holds Public Meeting to Address Agenda Items for the 33rd Session of the Codex Alimentarius Commission – Food Safety and Inspection Service

Posted on 10 May 2010 by admin

WASHINGTON, May 10, 2010 – The U.S. Department of Agriculture’s (USDA) Office of Food Safety is sponsoring a public meeting to provide information and receive public comments on agenda items and draft U.S. positions that will be discussed at the 33rd Session of the Codex Alimentarius Commission (CAC), to be held in Geneva, Switzerland, July 5-9, 2010.

The public meeting will be held on Tuesday, June 8, 2010, from 1 p.m. to 4 p.m., in Room 107-A, USDA, Jamie L. Whitten Building, 1400 Independence Ave. S.W., Washington, D.C. To participate through teleconference for the meeting, dial (866) 692-3158, and enter the passcode 5986642.

Documents and agenda items related to the 33rd Session of the CAC will be accessible at the Codex Web site at www.codexalimentarius.net/current.asp.

Codex was established in 1963 by two United Nations organizations, the Food and Agriculture Organization (FAO) and the World Health Organization (WHO). Through adoption of food standards, codes of practice and other guidelines developed by its committees, and by promoting their adoption and implementation by governments, Codex seeks to protect the health of consumers and ensure fair practices in the food trade.

For further information about the 33rd Session of the CAC and about the public meeting, contact Barbara McNiff by mail at U.S. Codex Office, 1400 Independence Ave. S.W., Room 4861-S, Washington, D.C. 20250, by phone at (202) 690-4719 or by fax at (202) 720-3157. Interested U.S. parties are also invited to request information about the 33rd Session of the CAC and about the public meeting, as well as submit comments about the 33rd Session of the CAC, electronically to the following e-mail address: Barbara.McNiff@fsis.usda.gov.

Written comments on the public meeting may be offered at the meeting or sent by e-mail to the U.S. Delegate for the 33rd Session of the CAC, Karen Stuck, U.S. Codex Manager, at USCodex@fsis.usda.gov. Written comments should state that they relate to activities of the 33rd session of the CAC.

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Activists want GMO foods labelled at upcoming Codex meeting Read more: http://www.digitaljournal.com/article/291475#ixzz1augVDf00

Posted on 02 May 2010 by admin

The United Nations Codex Alimentarius, the commission on food labelling, referred to around the world as ‘Codex,’ is meeting in Quebec City from May 3 to 7th.

The Codex is extensive, with 13 volumes that “govern global food quality and safety standards”. The Codex is put together by the World Health Organization and the Food and Agriculture Organization, both United Nations bodies. The Codex Commission, which has existed since 1963 has over 170 members, and the main purposes of the Codex Commission are

“… protecting the health of consumers and ensuring fair practices in the food trade, and promoting coordination of all food standards work undertaken by international governmental and non governmental organizations.”

The Codex, however, is shaped through the input of food producers, processors and governments. The Codex has a bad taste in certain circles around the world, where people claim the Codex is the biggest threat to natural and whole foods, including organic foods. The Alliance for Natural Health Europe (ANHE) has handily summed up the major rumours circulating the globe about Codex. The biggest problem with the Codex, according to the ANHE,

“… It aims to tell us what is safe, but in the process often uses criteria that are manipulated to support the interests of the world’s largest corporations.”

The upcoming negotiations will discuss the labelling of genetically modified foods (GM) and if adopted,

“… could permit countries to establish labeling regimes without the threat of challenge via the World Trade Organization.”

said the Canadian Biotechnology Action Network (CBAN) in a recent press release. CBAN also said Canada often follows the US on issues involving GM foods, resulting in the promotion of GM interests over consumer interests.

Although Canada is hosting the upcoming Codex meeting, Canada has not yet stated its position on the upcoming negotiations, a tactic CBAN criticised.

“… Though Canada has not yet released its official position, as in the past it seems to be similar to that of the U.S., which is actually trying to stop the negotiations from continuing.

These delaying tactics are unacceptable, the more so because they are based on false arguments such as an insistence that there is no difference between GM food and food produced using conventional methods, and that the truth of GM labels cannot be verified. Canada and the U.S. appear to be negotiating in bad faith and are among the last countries resisting GM labeling.”

CBAN is leading a letter writing campaign that invites Canadians to join a coalition of nine groups who are lobbying Canada’s Health Minister, Leona Aglukak to

“… demand that the Minister give instructions to the Canadian government delegation to support a position that recognizes the rights of all countries to adopt rules on GM foods labeling.”

CBAN explained why letters are to go to Health Minister Leona Aglukak, stating

“Usually letters on the topic of GE labeling would go to the Canadian Food Inspection Agency, but Canadian participation in Codex is coordinated by Health Canada.”

While not part of the CBAN campaign, the Green Party of Canada issued a statement on April 29th supporting the labelling of GM foods, with the rationale

“… Developing countries are seeking support from Codex for their right to label GM foods as they see fit. It’s widely speculated that Canada and the US will try to shut down negotiations on GM labelling so that developing countries will have no protection from challenges through the World Trade organization.”

Leader Elizabeth May said

“Polls show that over 80% of Canadians want mandatory labelling of GM foods. Harper must abandon his opposition to GM labelling and instruct his delegation to the Codex meeting to respect the will of Canadians and other countries.”

The Codex Commission states its position on GM foods by saying

“… Codex has adopted principles and guidelines to assess food safety of foods derived from recombinant-DNA plants, animals and microorganisms. If a government chooses to build a regulatory mechanism to address the food safety of so-called GM foods, then they can use Codex text as a basis for it. This being said, each government is free to adopt its own policy as to the use of GM organisms in the agriculture and other sectors.

At the moment, there are no internationally-agreed recommendations on the food labelling of GM foods. Governments are therefore applying their own regulations.

Codex has developed standards and a code of practice to effectively apply the irradiation technology to improve food safety, together with guidance on the labelling of irradiated foods. However, it is left to governments to determine their own approach to the use of food irradiation.”

Read more: http://www.digitaljournal.com/article/291475#ixzz1augREjSz

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Supreme Court Hears Case on GM Alfalfa Ban

Posted on 27 April 2010 by admin

The U.S Supreme Court yesterday questioned the authority of a lower court to ban “roundup ready alfalfa” (RRA), in the high-profile case of Monsanto Co. v. Geertson SeedFarms. Roundup Ready alfalfa seed is genetically modified to resist the herbicide called Roundup. The case is more about the legality of the ban than the safety of RRA plants and is being closely watched by all sectors of food and agri-business, and by environmental organizations.

In 2005 the U.S. Animal and Plant Health Inspection Service (APHIS) approved the planting of RRA. In 2007 the Center for Food Safety took the issue to U.S. District Court in San Francisco which banned the alfalfa until a comprehensive EIS (Environmental Impact Study), required under the National Environmental Policy Act (NEPA), could be carried out.

Monsanto Co. and petitioner Forage Genetics Inc. (FGI) made claim in Supreme Court that the district court’s ban was unlawful because the court did not seek to determine evidence of future harm due to RRA, implying that a NEPA violation alone is grounds for a ban. Monsanto argued that the injunction caused undue financial harm to farmers, and in courtdocuments the petition argued that the actual risk of cross-pollination from GE alfalfa is “exceedingly small.”

Organic food producers and environmental groups say that RRA will cause widespread environmental and economic damage. Alfalfa is pollinated by bees and other flying insects and it is only a matter of time before cross-pollination occurs. Food with GE genes cannot be considered organic and cross-pollination with modified alfalfa would cause great damage to the organic food market, according to the groups.

The Center for Food Safety cited seven briefs submitted in support of Geertson, by over two dozen natural food companies and producers, as well as by the Natural ResourcesDefense Counsel, the Union of Concerned Scientists, and the Humane Society.

Monsanto said 18 entities submitted briefs to support its position that RRA should not be banned. They are the American Farm Bureau Federation, Biotechnology Industry Organization, American Seed Trade Association, American Soybean Association, National Alfalfa and Forage Alliance, National Association of Wheat Growers, National Cotton Council and National Potato Council, Sugarbeet Growers Association, U.S. Beet Sugar Association and National Corn Growers Association, The Chamber of Commerce of the United States of America, American Petroleum Institute, National Association of Home Builders, and CropLife America, The Washington Legal Foundation, Allied EducationFoundation, and Pacific Legal Foundation, according to a Monsanto news release.

The case may become a moot point if the USDA passes regulation, now under consideration, that would require all bio-engineered plants undergo a thorough environmental impact statement.

The Supreme Court is expected to announce a decision before late June.

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Obama USDA Poised to Take Away Our Right to GMO-Free Food

Posted on 21 January 2010 by admin

Don’t believe Monsanto’s green-washing. Genetically modified organisms (GMOs), aren’t meant to feed the world or survive the evermore frequent droughts and floods brought on by global warming – they’re designed to sell Monsanto’s herbicide Roundup and the patented “Roundup Ready” genes now spliced into millions of acres of corncottonsoycanolasugar beets and alfalfa. A 2009 study showed that, in 13 years, Roundup Ready crops increased herbicide use by 383 million pounds.

During the Bush administration, the movement to stop GMOs was making progress. Reflecting public concern over GMOs, in 2007, a Federal court ruled that the Bush USDA’s approval of Roundup Ready alfalfa violated the law because it failed to analyze risks such as the contamination of conventional and organic alfalfa and the development of “super-weeds.” The court banned the planting of GM alfalfa until USDA completed a rigorous analysis of these impacts. The Ninth Circuit Court of Appeals twice affirmed the national ban on Roundup Ready alfalfa planting, but Monsanto is appealing. They’re taking organic alfalfa farmers all the way to the Supreme Court!

Barack Obama, despite promising us “change we can believe in,” is unfortunately turning out to be just as pro-GMO as the preceding Bush and Clinton administrations, packing the USDA and other government bureaucracies with Monsanto men and biotech cheerleaders such as former Iowa Governor, Tom Vilsack, named “Biotech Governor of the Year” in 2001, now serving as USDA Secretary. Vilsack, notorious for flying around in a Monsanto company jet during one of his previous election campaigns, is now busy trying to get the court-ordered ban on Roundup Ready alfalfa lifted by issuing a new draft environmental impact statement (EIS) that denies or downplays the obvious environmental and human health hazards of GM alfalfa.

Alfalfa is the fourth most widely grown crop in the U.S. and a key source of dairy forage and hay. The first perennial crop to be genetically engineered, GM alfalfa can regenerate itself from its root-stock. It is open-pollinated by bees, which can cross-pollinate at distances of several miles, spreading Monsanto’s patented, foreign DNA to non-GMO and organic crops. Widespread GMO-contamination of organic alfalfa is inevitable if the Obama Administration successfully distorts science and ignores public opinion and allows Monsanto’s GM Roundup Ready alfalfa to be planted across the U.S.

Mounting evidence shows damage to animals and humans from unlabeled and untested Frankenfoods. Consumers who ingest GM alfalfa are likely risking their health; since even the USDA’s EIS admits that, “acute toxicity in mice was observed.”

According to the EIS, consumers who ingest foods with residues of Monsanto’s Roundup herbicide may experience “general and non-specific signs of toxicity from subchronic and chronic exposure to glyphosate includ[ing] changes in liver weight, blood chemistry (may suggest mild liver toxicity), liver pathology, and weight of the pituitary gland.”

The EIS warns that, “Based on upper estimates of exposure … infants consuming fruit and all age groups consuming vegetables may be at risk of adverse effects associated with acute exposure to glyphosate [the active ingredient in Roundup] residues.”

Consuming milk and meat from animals fed crops that are genetically engineered is also risky. In Europe, where farmer and consumer rejection has kept GMO crop acreage to a bare minimum, massive quantities of GMO-tainted animal feed is imported from the U.S. and a survey of 60 samples of 12 different milk brands sold in stores in Italy demonstrated the presence of GM maize sequences in 15 (25%) and of GM soybean sequences in 7 samples (11.7%).

Most consumers, especially organic consumers, are determined to avoid Roundup Ready alfalfa, and meat and dairy products derived from animals ingesting Roundup Ready alfalfa, but according to the EIS, we don’t have that right because, “At the present time, there is no policy regarding the unintended presence of GE (genetically engineered) material in organic products or food, consistent with the fact that the NOP (National Organic Program) is a process-based program for certifying a farm or production system as organic, and not a product-based program that tests or certifies individual products as organic.”

We must stop the Obama administration from taking away our right to grow and consume organic and GMO-free food. The “change we believe in” is a healthy and sustainable future based upon organic food and farming and a green economy.

Follow Ronnie Cummins on Twitter: www.twitter.com/OrganicConsumer

source: huffingtonpost.com

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