Guest post by Kathleen Barnes
As I prepare to put in my garden this year, I feel a little like some whacko-zombie apocalypse fanatic. I am on a fervent mission to find non-GMO seeds and plants.
It’s not as easy as you might think since Monsanto, the father of Frankenfoods and RoundUp (what a pair!) has not only managed to protect itself against lawsuits from consumers whose health is damaged by its GMO products, it has also managed to buy up most of the seed companies and insert genetically modified organisms (GMOs) into their products.
The day is not far off when it will be impossible to buy seeds that have not been modified.
Until very recently, Monsanto had targeted corn, canola, soy and cotton, but now its gobbled up the market for the seeds you and I plant in our backyard gardens. Monsanto now owns 90 to 95 of all seed companies in the U.S. While Monsanto says it has no intention of making all seeds GMO, I can only say: If you believe that, I’ve got a bridge I’d like to sell you.
Let’s back up a few weeks to March 29 when President Obama signed into law, which has been dubbed the Monsanto Protection Act. The bill allows Monsanto to promote and plant genetically modified organisms (GMOs) and genetically engineered (GE) seeds and precludes the courts for litigating any cases contending the products are unsafe.
This unprecedented legal protection also gives Monsanto a green light to continue producing and expanding its market for GMO crops and seeds.
The danger now is that according to US laws, Monsanto always wins, even if its experimental crops are proven to be hazardous to human health and even if they cause a runaway crop plague. Now, the American government has given away the judicial power to prohibit the planting and harvesting GMO crops in almost any case.
Zombie apocalypse, indeed!
GMO foods have been scientifically linked to obesity, diabetes, immune system alterations and impaired ability to digest protein. malfunction. The Bt-toxin introduced by Monsanto in the 1990s to kill insects has now been found in the blood of 67 percent of all women, 93 percent of all pregnant women and 80 percent of umbilical cord blood in their babies.
That’s just the tip of the iceberg. At least we, as consumers, have the right to know what we’re eating. Well-financed corporate interests helped defeat the GMO labeling amendment in California. Washington state has a labeling initiative pending. More than 60 countries now requires GMO labeling, but not the U.S. This is everyone’s fight, so I encourage you to get involved.
Back home, I’m seeking out heirloom seeds and plants for my garden. I found a good list at Garden of Eatin’that not only give us a very short list of seed companies that have signed a non-GMO statement for their products and a much longer list of those that are either owned by Monsanto or have at least some GMO seeds.
Today’s revolution is with our pocketbooks. Don’t buy products from companies that have bought into the Monsanto lie.
This is a complex issue that I’ll be visiting and re-visiting frequently in the future. Stay tuned. Your health and mine and the health of the planet for the next seven generations depends on it.
All content is written by Kathleen Barnes and may be used freely if unedited and attributed.
Showing posts with label GMOs. Show all posts
Showing posts with label GMOs. Show all posts
Friday, May 17, 2013
Tuesday, July 10, 2012
The Right to No --- GMOs Must Go
By James J. Gormley
Her chariot is an empty hazelnut [ . . .]
And in this state she gallops night by night [ . . .]
o'er lawyers' fingers, who straight dream on fees
--- Mercutio, Shakespeare's Romeo and Juliet, Act 1, Scene 4
Not that lawyers only think of (or dream about) fees, however it is worth noting that when Californians vote this November 6th on the Right to Know Genetically Engineered Foods Act (aka the GE Foods Mandatory Labeling Initiative), they will not only, fortunately, be taking an historic stand for consumer rights but also, unfortunately, throwing down a wild card on the table, one that could potentially open up the floodgates to private actions (lawsuits) against makers of all manner of raw and processed foods, food supplements and packaged goods, in short: 60 to 80 percent of products on store shelves in The Golden State.
Her chariot is an empty hazelnut [ . . .]
And in this state she gallops night by night [ . . .]
o'er lawyers' fingers, who straight dream on fees
--- Mercutio, Shakespeare's Romeo and Juliet, Act 1, Scene 4
Not that lawyers only think of (or dream about) fees, however it is worth noting that when Californians vote this November 6th on the Right to Know Genetically Engineered Foods Act (aka the GE Foods Mandatory Labeling Initiative), they will not only, fortunately, be taking an historic stand for consumer rights but also, unfortunately, throwing down a wild card on the table, one that could potentially open up the floodgates to private actions (lawsuits) against makers of all manner of raw and processed foods, food supplements and packaged goods, in short: 60 to 80 percent of products on store shelves in The Golden State.
In the case of non-processed foods, the words ‘Genetically Engineered” will appear on the front of the package; in the case of processed foods with a variety of ingredients, the words “Partially Produced with Genetic Engineering” or “May be Partially Produced with Genetic Engineering” will appear on the front or back of the package. I wish the term “Produced with Genetically Modified Organism [GMO] Ingredient Technology,” or something similar, had been chosen instead.
Natural Genetic “Engineering” … and Frankenfoods
Why? Because as early as 8,000 B.C. farmers had already domesticated many wild food-plant species, with growers having selectively bred thousands of different strains, each with its own hereditary genetic material, or “germ plasm.”
While our ancestral farmers did not understand hybridization, and could not engage in mutation breeding (exposing plants to chemicals or radiation to create beneficial mutations) or utilize genetically modified organism (GMO) technology, clearly plant husbandry was an early version of genetic engineering: farmers using what they knew about a plant to select for specific desirable traits to develop improved varieties.
Examples of crops that are the product of traditional hybridization techniques include grapefruit (which was a cross of two different citrus fruits) and maize (a plant that was domesticated in Mexico 10,000 years ago that produced very tiny cobs).
Animals have not been immune to human-made genetic crossing as well, and centuries of domestication and breeding for specific traits. In this example, we of course have mules (a horse and donkey cross) and anywhere from 150 to 600 breeds of domesticated dogs all bred to bring out certain characteristics.
This is of course far different from producing a hybrid plant that could never have existed in nature, especially using genes from one species (even an alien species, like fish) to create changes in another species.
![]() |
| Courtesy azrainman.com |
While the fish tomato thankfully never made it to the produce aisle, other cross-species combos have. A gene from the Bacillus thuringiensis bacteria was inserted into corn to combat a corn-eating worm; today, 63 percent of the U.S. corn crop uses this Franken-seed.
The use of genetically engineered bacteria to create nutraceutical compounds has had a disastrous track record. Case in point: in 1989 over 1,500 people became very sick and nearly 40 died as a result of ingesting contaminated L-tryptophan that had been made by a foreign pharmaceutical company using genetically engineered bacteria.
This is a perfect example of the grave concerns over 90 percent of Americans have regarding GMOs and why they want products with GMOs to be labeled as such.
Europe Has Taken A Hard Line Against GMOs; the U.S. Government Is a Huge GMO Advocate
The European Union (EU) took a more aggressive approach, at least initially, with a six-year moratorium on gene-altered products than ran from 1998 to 2004. Sadly, the U.S., Canada and Argentina challenged it in court and, in 2006, the World Trade Organization (WTO) ruled that the EU ban was illegal.
At the time, Eric Gall of Greenpeace told EurActiv.com that "All this verdict proves is that the WTO is unqualified to deal with complex scientific and environmental issues, as it puts trade interests above all others. Its only effect has been to reinforce the determination of EU countries to resist bullying by pro-GE governments and to say no to GE crops and food."
Case in point: After the May 2006 WTO ruling, American exports of rice to Europe were stopped when a majority of the U.S. crop was confirmed to be contaminated with unapproved engineered genes.
In the interim, in April 2004 Hugo Chavez had announced a total ban on genetically modified (GM) seeds in Venezuela and, in January 2005, the Hungarian government had issued a ban on the importation and planting of GM maize seeds, which was subsequently upheld by the EU .
Which brings us back to December 18 of 2006, when the EU’s environment ministers officially rejected the WTO’s ruling, specifically the proposal to force Austria to lift its bans on GM foods and crops. National bans have also been issued in Bulgaria, France, Germany and Ireland.
All in all, according to journalist Jeremy Stahl in the June 14, 2012 edition of Slate.com, public opinion in the EU has for years been adamantly against GMOs. “European policymakers have responded to their constituents rather than their scientists, and only two GM crops have been approved for farming in EU states, while 90 have been permitted by the FDA for use in the United States.”
That being said, the tide may be turning in the other direction in Europe just as the U.S. (California most prominently) is shifting back to where the EU was. The European Food Safety Authority (EFSA) rejected the French ban on GM corn. While the EU Commission is deciding how to enforce the ruling, EU’s health commission has said that it “could now ask France to lift the ban,” wrote Stahl.
Will GMO Labeling Help or Confuse Consumers?
Peggy Lemaux, Ph.D., a cooperative extension specialist at the University of California, Berkeley who manages a website on biotechnology told Eliza Barclay of National Public Radio (NPR) in a May 14, 2012, interview, that the GE label may “scare less savvy consumers away from affordable, healthful foods.”
The July 5th issue of trade magazine, Retail Leader, noted the concerns of opponents to the California initiative who ask readers to “consider how costs could increase and small businesses could be hurt if the mandate encouraged frivolous lawsuits against companies that didn’t carry a GMO label but were sued nonetheless.”
As I noted in my April 3rd, 2012 commentary, the last time there was a mandatory labeling initiative in California was 1986, when “The Safe Drinking Water and Toxic Enforcement Act” (aka Proposition 65, or Prop 65) was passed into law via a direct voter initiative.
Another Gravy Train for Lawyers and Their Straw Man Plaintiffs?
Prop 65, a well-intended yet disastrously misguided law that should instead be called the “Private Attorney Enrichment Via Straw Man Plaintiffs Act,” has done little to protect consumers but has done much to hurt businesses operating in or selling into California, including dietary supplement companies.
![]() |
| Courtesy Robert Huffstutter |
And lawsuits for GMO labeling are a very real prospect, indeed.
While the organizers of the California initiative point to the fact that the lawsuit will not authorize the awarding of Prop 65-like “bounty hunter fees” to lawyers who bring suits, which is true, what is not brought out is that (1) anyone can sue to enforce the new statute, (2) they can be awarded their attorney fees and costs of bringing suit, and (3) they don’t have to prove anything---such as facts, damage or loss---or to even win the case as such for the Court to award them fees.
In a legal analysis of the initiative by James C. Cooper, JD, Ph.D., entitled “Proposition 65 and the Proposed California Right to Know Genetically Engineered Foods Act: A Comparison of Litigation Incentives,” Cooper wrote: “The adoption of Label GMO likely would result in private lawsuits to enforce its provisions.”
In an interview with The Gormley Files, when asked as to how widespread the “private lawsuit business will be,” Cooper said: “As I note in my paper, because there is a private right of action, we can expect private suits, however there are reasons to believe that the GMO ballot initiative will not yield the levels of abusive litigation associated with Prop 65.” We shall see.
Will Labeling Stop the Virulent Spread of GMOs?
And while it is hoped that GMO labeling will allow consumers to vote with their pocketbooks and that they will choose the few remaining products over the 70 to 95 percent of products contaminated with GMOs, we don’t know this for certain, regardless of whatever poll numbers suggest.
As California consumers make those choices over the coming years, growers and countries will continue to abandon old, land-race crops in favor of GE, single-variety monocultures, thus setting the stage for the entire world’s complete, and utter, destruction, as a single disease, or only a few of them, could then wipe out the planet’s food supply before we could stop it.
![]() |
| Deforestation in the Pacific Northwest |
It is predicted that by the year 2050, 25 percent of the world’s 250,000 plant species will disappear due to deforestation, the shift to genetically uniform crops, over-grazing, water control projects and urbanization.
In April 1991, plant geneticist Jack Harlan (1917-1998) warned: “The diversity of our genetic resources stands between us and starvation on a scale we cannot imagine.”
To prevent worldwide disaster scenarios such as this, groups are tracking down the wild relatives of modern crops in habitats believed to favor their survival, then preserving their germ plasm in a global network of seed banks (or gene banks)---such as the Svalbard Global Seed Vault---and protected natural sites.
However, better oversight and controls need to be devoted to these efforts, as not only have many seed banks fallen into decay but the funding for these efforts appears to have been, thus far, subverted by the same company that rules the GMO roost.
The Way Forward?
Assuming the ballot initiative passes, only time will tell as to who will truly benefit and who will truly lose, especially as similar initiatives are on the hopper in several other states and the Federal government.
But the bigger question is this: Why don’t we push for a full ban of GMOs?
It’s no accident that only 5 percent of food in Europe contains GM traces, which is thanks to a “zero tolerance” policy that the EU has had.
For Europe, moving to zero would be a lot easier than for us, however a staged approach to eliminating GMOs for U.S. agriculture and the food industry might just work, similar to the milestones associated with vehicle emission requirements (e.g., hydrocarbons, carbon monoxide and nitrogen oxide) staged for five milestone years, including those coming up in 2017 and 2025.
Perhaps modest incentives and tax breaks can be offered to GM seed makers if they agree to phase out the development and sale of GM seeds and GM-seed-specific pesticides and help farmers in remediation efforts to restore their crops to non-patented, non-GM varieties, and agree to cease the persecution of farmers for using traditional, seed-saving practices that have been part of agriculture for 10,000 years. Certainly, the U.S. Department of Agriculture (USDA) would need to phase out its GE/GM development mission, as well.
All of this will take a great deal of political will driven by consumer grassroots’ demand, but it can be done, as we have seen in Europe.
A world free of GM plants and crops may well be the ultimate answer. Not just the “The Right to Know,” but the “Right to No.”
As in no GMOs.
Wednesday, January 12, 2011
Eeek! Snakes on a Plate!
How the Latest Health “Solutions” Are Like a Comedy Turned Scary!
By James J. Gormley
When I was a kid, one of my “absolute favorite” movies was Stanley Kramer’s madcap 1973 comedy, It’s A Mad Mad Mad Mad World.
When I first saw it on CBS in 1978, I loved the antic chaos, the slapstick stunts and the total zaniness of the movie --- hard to not be a sillifest when you have the likes of Milton Berle, Sid Caesar, Ethel Merman, Mickey Rooney and Jonathan Winters, to name only a few of the comedic greats who graced the celluloid of this film.
What does this have to do with health freedom or health politics? Well, unfortunately: plenty.
In fact, America seems to be in the midst of an unprecedented convergence of varied and sundry strange health “solutions” that are no less wacky than Kramer’s cinematic masterpiece but, unfortunately, not funny … and also rather horrific.
Here are a couple of the latest “strange but true” ideas that would be laughable if they weren’t attracting widespread media attention --and even some supporters!
Food from cloned cattle or cloned meat grown in vats
According to Spence Cooper in a blog post on FriendsEAT.com: “Recent news reports indicate some U.S. cloned cattle have been created from the cells of dead animals […] And since the U.S. approved cloning over two years ago, you may have already grilled a cloned steak this summer from beef cells extracted from a dead carcass.”
Approved by the U.S. Food and Drug Administration (FDA) in January 2008, the alleged purpose of using the technology would be to improve the taste or “quality” of meat and milk that we all consume every day. Because of the cost of cloned cows ($15-20,000 a cow), it is predicted that the offspring of cloned animals will be used (or consumed), not the clones themselves.
Small consolation that. When even the farmers are against something like this, you know it must be really bad. In a written statement at the time, the National Farmers Union said: “Consumers have the right to know if the food they feed their families comes from a cloned animal.”
In addition to ethics, the “right to know” is really what it boils down to: labeling and for consumers being able to make informed choices as to whether they are buying food from clones, cloned offspring, GMOs or what have you, although labeling will most likely not be required.
As I wrote in a Nutrition Industry Executive article, in December 2006, entitled “The FDA’s Strange New World,” the FDA had begun campaigning for cloned animals as early as 2001. In the January-February 2001 issue of FDA Consumer, an FDA writer enthused: “Transgenics can turn animals, such as cows, sheep and goats, into pharmaceutical factories.” Gee, isn’t that a reassuring dream?
“Should there be any limits as to how far we as a species can go in manipulating the fabric of life?” I asked in Better Nutrition magazine back in October 1997. “Or should we, like Dr. Frankenstein in Mary Shelley’s nightmare, proceed with the ultimate arrogance that nature is not only up for our unlimited exploitation but for our boundless tinkering, as well?”
Statins with that burger?
In a paper that ran in The American Journal of Cardiology, Dr. Darrel Francis and colleagues from Imperial College London (U.K.) suggest that giving out statin drugs to people at fast-food restaurants will help reduce heart disease risks caused by the fat-drenched meals.
The British Heart Foundation (BHF), which funded the study, is none too pleased with the suggestion of the “MacStatin” that the authors propose. In a BHF blog post by Dr. Mike Knapton, the foundation says:
“Promoting a pill for junk food would lead us towards medicalizing a huge swath of our population when really people need to take more responsibility for their own health.”
Indeed.
If that represents a “holistic approach,” then I imagine the authors have a bridge to sell me, or to themselves.
Gormley Take-Away: I envisage a future in which food is food --- not grown in Franken-vats or derived from cloned animals or plants or spiked with statin drugs or any other pharmaceutical. I hope that we all can work toward such a tomorrow and that we can leave the comedies and fright-fests to the movie makers, not on our plates.
By James J. Gormley
When I first saw it on CBS in 1978, I loved the antic chaos, the slapstick stunts and the total zaniness of the movie --- hard to not be a sillifest when you have the likes of Milton Berle, Sid Caesar, Ethel Merman, Mickey Rooney and Jonathan Winters, to name only a few of the comedic greats who graced the celluloid of this film.
What does this have to do with health freedom or health politics? Well, unfortunately: plenty.
In fact, America seems to be in the midst of an unprecedented convergence of varied and sundry strange health “solutions” that are no less wacky than Kramer’s cinematic masterpiece but, unfortunately, not funny … and also rather horrific.
Here are a couple of the latest “strange but true” ideas that would be laughable if they weren’t attracting widespread media attention --and even some supporters!
Food from cloned cattle or cloned meat grown in vats
According to Spence Cooper in a blog post on FriendsEAT.com: “Recent news reports indicate some U.S. cloned cattle have been created from the cells of dead animals […] And since the U.S. approved cloning over two years ago, you may have already grilled a cloned steak this summer from beef cells extracted from a dead carcass.”
Approved by the U.S. Food and Drug Administration (FDA) in January 2008, the alleged purpose of using the technology would be to improve the taste or “quality” of meat and milk that we all consume every day. Because of the cost of cloned cows ($15-20,000 a cow), it is predicted that the offspring of cloned animals will be used (or consumed), not the clones themselves.
Small consolation that. When even the farmers are against something like this, you know it must be really bad. In a written statement at the time, the National Farmers Union said: “Consumers have the right to know if the food they feed their families comes from a cloned animal.”
In addition to ethics, the “right to know” is really what it boils down to: labeling and for consumers being able to make informed choices as to whether they are buying food from clones, cloned offspring, GMOs or what have you, although labeling will most likely not be required.
As I wrote in a Nutrition Industry Executive article, in December 2006, entitled “The FDA’s Strange New World,” the FDA had begun campaigning for cloned animals as early as 2001. In the January-February 2001 issue of FDA Consumer, an FDA writer enthused: “Transgenics can turn animals, such as cows, sheep and goats, into pharmaceutical factories.” Gee, isn’t that a reassuring dream?
“Should there be any limits as to how far we as a species can go in manipulating the fabric of life?” I asked in Better Nutrition magazine back in October 1997. “Or should we, like Dr. Frankenstein in Mary Shelley’s nightmare, proceed with the ultimate arrogance that nature is not only up for our unlimited exploitation but for our boundless tinkering, as well?”
In a paper that ran in The American Journal of Cardiology, Dr. Darrel Francis and colleagues from Imperial College London (U.K.) suggest that giving out statin drugs to people at fast-food restaurants will help reduce heart disease risks caused by the fat-drenched meals.
The British Heart Foundation (BHF), which funded the study, is none too pleased with the suggestion of the “MacStatin” that the authors propose. In a BHF blog post by Dr. Mike Knapton, the foundation says:
“Promoting a pill for junk food would lead us towards medicalizing a huge swath of our population when really people need to take more responsibility for their own health.”
In the Cardiology article, the authors write: “We envisage a future in which fast food restaurants encourage a holistic approach to healthy eating. On ordering an unhealthy meal, the food will arrive labeled with a warning message […] and on the tray, next to the ketchup, will be a new and protective packet, ‘MacStatin,’ which could be sprinkled onto a Quarter Pounder or into a milkshake.”
Indeed.
If that represents a “holistic approach,” then I imagine the authors have a bridge to sell me, or to themselves.
Gormley Take-Away: I envisage a future in which food is food --- not grown in Franken-vats or derived from cloned animals or plants or spiked with statin drugs or any other pharmaceutical. I hope that we all can work toward such a tomorrow and that we can leave the comedies and fright-fests to the movie makers, not on our plates.
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Tuesday, October 28, 2008
Codex—U.S. and global implications
By James J. Gormley
Codex Alimentarius is Latin for “food code” or “food law”. The Codex Alimentarius Commission (CAC) is one of the international bodies recognized by both international treaties and the World Trade Organization (WTO) for establishing global food standards.
According to the advocacy organization Public Citizen, recent international trade agreements have caused a radical change in the impact of Codex. The General Agreement on Tariffs and Trade (GATT) of 1994 and other treaties have altered the nature of Codex standards by “designating Codex as the international body” establishing internationally recognized food safety standards for use in trade.
After global trade negotiations in 1994, several international agreements were established, agreements that were intended to blur the lines of distinction among different national regulatory requirements regarding public health and food safety and to eliminate barriers to international trade.
According to the New Zealand Food Safety Authority, “Codex standards are considered scientifically justified and are accepted as international yardsticks,” wrote the New Zealand authority in 2001. WTO member standards that differ from Codex standards may be challenged as trade barriers if they only allow lower levels that serve to restrict trade.
Critics Voice Concerns
According to the Center for International Development at Harvard University: “These measures are criticized by some who claim the agreements are too invasive and deny them sovereignty of domestic regulation. Others assert that the agreements do not go far enough and domestic regulation is often a form of protectionism. Developing countries protest that the standards promoted in the agreements lack their input and are dominated by the interests of developed countries.”
“In the highly contentious debate over genetically modified foods,” wrote the Center, “some non-governmental organizations argue that these agreements” make it hard for countries to make their own decisions as to, for example, simply banning or allowing GMOs for sale in their country.
Others have criticized Codex’ use of the same standards that apply to toxic chemicals and environmental hazards with food and dietary supplements.
Some observers have said that Codex’ application of the precautionary principle—banning something because it might be harmful—is hypocritical: it is applied to dietary supplements, where it is not needed, but it is not applied to toxic additives, where it is needed.
Other issues at stake
Codex is looking at what forms and potencies of vitamins and minerals should be allowed for international trade, allowing individual nations to restrict other forms and potencies. Codex does not currently address other ingredients used in dietary supplements.
Calls for inclusion of DHA (docosahexaenoic acid) and ARA (arachidonic acid), and exclusion of partially hydrogenated fats and high fructose corn syrup, in infant formula standards have seemingly fallen on deaf ears, as have many other issues, say some, including concerns about GMOs.
Sustainability is another issue on the Codex horizon that may impact how some U.S. companies operate in terms of ingredient sourcing and also in terms of rising global demand for eco-friendly harvesting and production.
So how does Codex affect me?
Codex can affect you in a few ways:
1. Its guidelines regarding risk assessment have the potential to support low potencies for nutritional ingredients; that impacts what is available on store shelves if the U.S. products have had to be dumbed down based on low potencies allowed in Europe and supported by Codex. Large companies that export rely on economies of scale that will encourage them to formulate for the broader world market with restricted forms and potencies.
2. There is the real risk that the US government may copy some of these foreign and international trade standards as maximum levels for its own citizens, thus restricting our right to buy the full range of currently available dietary supplements.
3. Codex’ foot-dragging on GMOs and unhealthful ingredients (such as trans fats and high fructose corn syrup) will encourage functional food and beverage manufacturers to continue to use these controversial cheap, fattening and sweetening substances.
Gormley Take-Away: While Codex apologists are telling you we have nothing to worry about and “the sky is falling” alarmists are saying that we have everything to worry about, very real concerns and opportunities, such as those outlined above, could get lost in the shuffle. Solution? Stay tuned to what our industry associations are saying about Codex but also stay tuned to what credible consumer health advocacy organizations are saying (such as Citizens for Health). That way, you will have different perspectives that are not always 180 degrees apart and which, together, offer you a balanced view, whether pro, con or wait-and-see.
Codex Alimentarius is Latin for “food code” or “food law”. The Codex Alimentarius Commission (CAC) is one of the international bodies recognized by both international treaties and the World Trade Organization (WTO) for establishing global food standards.
According to the advocacy organization Public Citizen, recent international trade agreements have caused a radical change in the impact of Codex. The General Agreement on Tariffs and Trade (GATT) of 1994 and other treaties have altered the nature of Codex standards by “designating Codex as the international body” establishing internationally recognized food safety standards for use in trade.
After global trade negotiations in 1994, several international agreements were established, agreements that were intended to blur the lines of distinction among different national regulatory requirements regarding public health and food safety and to eliminate barriers to international trade.
According to the New Zealand Food Safety Authority, “Codex standards are considered scientifically justified and are accepted as international yardsticks,” wrote the New Zealand authority in 2001. WTO member standards that differ from Codex standards may be challenged as trade barriers if they only allow lower levels that serve to restrict trade.
Critics Voice Concerns
According to the Center for International Development at Harvard University: “These measures are criticized by some who claim the agreements are too invasive and deny them sovereignty of domestic regulation. Others assert that the agreements do not go far enough and domestic regulation is often a form of protectionism. Developing countries protest that the standards promoted in the agreements lack their input and are dominated by the interests of developed countries.”
“In the highly contentious debate over genetically modified foods,” wrote the Center, “some non-governmental organizations argue that these agreements” make it hard for countries to make their own decisions as to, for example, simply banning or allowing GMOs for sale in their country.
Others have criticized Codex’ use of the same standards that apply to toxic chemicals and environmental hazards with food and dietary supplements.
Some observers have said that Codex’ application of the precautionary principle—banning something because it might be harmful—is hypocritical: it is applied to dietary supplements, where it is not needed, but it is not applied to toxic additives, where it is needed.
Other issues at stake
Codex is looking at what forms and potencies of vitamins and minerals should be allowed for international trade, allowing individual nations to restrict other forms and potencies. Codex does not currently address other ingredients used in dietary supplements.
Calls for inclusion of DHA (docosahexaenoic acid) and ARA (arachidonic acid), and exclusion of partially hydrogenated fats and high fructose corn syrup, in infant formula standards have seemingly fallen on deaf ears, as have many other issues, say some, including concerns about GMOs.
Sustainability is another issue on the Codex horizon that may impact how some U.S. companies operate in terms of ingredient sourcing and also in terms of rising global demand for eco-friendly harvesting and production.
So how does Codex affect me?
Codex can affect you in a few ways:
1. Its guidelines regarding risk assessment have the potential to support low potencies for nutritional ingredients; that impacts what is available on store shelves if the U.S. products have had to be dumbed down based on low potencies allowed in Europe and supported by Codex. Large companies that export rely on economies of scale that will encourage them to formulate for the broader world market with restricted forms and potencies.
2. There is the real risk that the US government may copy some of these foreign and international trade standards as maximum levels for its own citizens, thus restricting our right to buy the full range of currently available dietary supplements.
3. Codex’ foot-dragging on GMOs and unhealthful ingredients (such as trans fats and high fructose corn syrup) will encourage functional food and beverage manufacturers to continue to use these controversial cheap, fattening and sweetening substances.
Gormley Take-Away: While Codex apologists are telling you we have nothing to worry about and “the sky is falling” alarmists are saying that we have everything to worry about, very real concerns and opportunities, such as those outlined above, could get lost in the shuffle. Solution? Stay tuned to what our industry associations are saying about Codex but also stay tuned to what credible consumer health advocacy organizations are saying (such as Citizens for Health). That way, you will have different perspectives that are not always 180 degrees apart and which, together, offer you a balanced view, whether pro, con or wait-and-see.
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