Tag Archives: dietary supplements

Not All Dietary Supplements Are Created Equal

vitamin supplements

Purchasing dietary supplements you can trust can be tricky. Many manufacturers of nutraceuticals put their efforts into marketing and fancy labels, instead of placing the majority of their resources into creating a product of quality. The simple truth is that not all vitamins are created equal, and this article is intended to make you aware of some of the factors to keep in mind when making a purchasing decision.

Deceptive Labeling

Reading a label carefully and understanding what the label means is important when purchasing any product — especially vitamins. Some supplements don’t even contain what’s listed on the label. [1] The standards under which a vitamin or mineral is manufactured vary greatly from one company to another. Most companies don’t even manufacture their own product and just relabel someone elses formula and call it their own. Quality is the biggest factor in whether a supplement is absorbed and utilized by the body.

Understanding Mineral Potency

The elemental amount of calcium refers to the exact weight or potency of calcium a formula provides. The same is true for all other minerals. Some labels clearly list the elemental weight and are therefore simple to understand. For example, the elemental weight of a calcium supplement would be labeled as 250 mg of calcium contained within the supplement. If the calcium is combined with amino acids, like amino acid chelate, and it is given a general amount that doesn’t specify the calcium amount only, you must discern that the amount of calcium you are receiving is a bit more ambiguous.

A consumer would assume that a vitamin contains 100% potency from when it was manufactured. The fact is, only 90% of the vitamin potency listed on the label has to be in a product at the time of shipping. A vitamin starts losing its potency the minute it’s made. If not manufactured properly, a vitamin can be up to 50% weaker by the time you purchase the product. There are only minimal government guidelines, not requirements, regarding product storage (light, temperature, moisture, etc.), inventory rotation, particle granulation, or product coating, all of which affect the potency and quality of a vitamin.

Even though vitamins are perishable items, manufacturers are not required to prove that their products last for an extended period of time. Remember: light, heat, moisture, and oxidation rapidly destroy vitamin potency. After a vitamin is manufactured, vitamin companies are not required to conduct shelf life testing to see how product potency is affected over time.

Natural vs. Synthetic

The word natural can, unfortunately, sometimes be misleading. In the case of vitamin E, a manufacturer can use a blend of 10% natural vitamin E and 90% synthetic vitamin E and still label the product natural vitamin E. Using synthetic vitamin E, which is 40% cheaper, a manufacturer can greatly reduce the quality of a product to reduce his manufacturing cost.

To protect the consumer, a manufacturer should properly list the chemical name in the contents description. Natural vitamin E should be labeled ‘d-tocopherol’ and synthetic should be labeled ‘dl-tocopherol.’ [2] Natural vitamins have been regarded as having a 36% higher potency rate compared with their synthetic counterpart. Studies involving human subjects show that natural vitamin E is probably twice as effective as synthetic vitamin E. [3]

Are Your Vitamins Releasing The Energy You Need?

Since most vitamins cannot be manufactured in the body, they must be supplied by our diet. Vitamins are essential for releasing energy in foods, but our food supply does not guarantee an abundant source of nutrients. Therefore, it is best to eat a mostly raw diet with a wide variety of fresh vegetables, fruits, nuts, and seeds. This guarantees an assortment of essential vitamins that is helpful for the increased energy and feeling of well-being you are seeking.

The decrease in energy from the lack of proper nutrition sometimes surfaces in obvious forms; scurvy and rickets being prime examples. Often, the symptoms of a vitamin deficiency are much more subtle. Vitamin B12 deficiency, for example, takes years to become apparent, often disguising itself in the form of lethargy, depression, and neuropsychiatric symptoms. [4]

Always purchase vitamins and other dietary supplements from companies you can trust. How do you know you can trust them? They produce all of their own products themselves, sourcing only high-quality, organic ingredients.


  1. David Kroll. New York AG Fires Round 2 Against Herbal Dietary Supplement Makers. Forbes.
  2. Maret G. Traber, Ph.D., Scott W. Leonard. The Alpha-tocopherol Transfer Protein and Vitamin E Adequacy. Oregon State University. The Linus Pauling Institute.
  3. Philip L. Harris, James L. Jensen, Milton Joffe, and Karl E. Mason. Biological Activity of Natural and Synthetic Tocopherols. The Journal of Biological Chemistry. 1944, 156:491-498.
  4. Langan RC, Zawistoski KJ. Update on vitamin B12 deficiency. Am Fam Physician. 2011 Jun 15;83(12):1425-30.

Dr. Edward F. Group III, DC, NP, DACBN, DCBCN, DABFM has studied natural healing methods for over 20 years and now teaches individuals and practitioners all around the world. He no longer sees patients but solely concentrates on spreading the word of health and wellness to the global community. Under his leadership, Global Healing Center, Inc. has earned recognition as one of the largest alternative, natural and organic health resources on the Internet.

The FDA’s New Food Label Guidelines – A Sneak Attack On Your Dietary Supplements

      By Scott C. Tips, President NHF

fda protects big pharma

In a glitzy roll-out last month featuring First Lady Michelle Obama and Food and Drug Administration (FDA) Commissioner Dr. Margaret Hamburg, the FDA proudly announced its first major changes to nutrition and supplement labeling in 20 years.[1]  If the FDA gets its way, you will see a large number of formatting and placement changes made to the current Nutrition Facts panel on food labels and to the Supplement Facts panel on dietary-supplement labels.[2]  The FDA’s example of their proposed changes appears below.

nutrition labels

But while the food industry and everyone else is focusing on the format changes, new wording, and the snazzy design set forth in the 109 pages of the FDA’s Proposed Rulemaking, there – hidden in plain view like the Purloined Letter – is the real danger to our health: The FDA is harmonizing our vitamin-and-mineral levels down to the same ridiculous levels of Codex Alimentarius that NHF has fought at Codex for more than a decade.  Not 100% harmonization, but mostly.  Those dirty sneaks.

NHF First to Call Attention to This Danger

NHF was the first to raise the alarm about this danger with my article in Whole Foods Magazine,[3] which drew the striking parallel between the FDA’s proposed new Reference Daily Intakes (RDIs) for vitamins and minerals and the Nutrient Reference Values (NRVs) being pushed globally at the Codex level.  The FDA’s sneaky harmonization of vitamin-and-mineral daily levels downward to, in most cases, those miserably insufficient levels that the National Health Federation has fought at Codex meetings since 2004 is the biggest of all dangers in the new FDA Proposed Rulemaking for Food Labels.

It is heartening to see that other health-freedom organizations have read my words, taken them to heart, and then repeated my warning message to the general public.  We need more people to jump on the bandwagon.  This danger must be recognized, publicized widely, and stopped completely; and NHF encourages everyone to spread the word by sharing this article.

The Danger

Ever since the National Health Federation’s victory at the 2009 Codex Committee on Nutrition and Foods for Special Dietary Uses (CCNFSDU) meeting (where an Australian-led attempt to reduce, across the board, vitamin-and-mineral NRVs was rebuffed), Australia and other Codex delegations have continued pushing their anti-nutrient agenda. Conspicuously silent during these debates has been the U.S. delegation.  Now we know why.

Interestingly enough, Codex Alimentarius is mentioned in the FDA’s Proposed Rulemaking multiple times.  And with this Proposed Rulemaking, the FDA wants to dumb down our RDIs to the abysmally low Codex levels with no fewer than eight vitamins and minerals, while one (folic acid) already matches the Codex NRV and two others are within spitting distance.  In the case of Biotin, FDA proposes to cut its Reference Daily Intake by 90% in order to match the Codex value![4]

The FDA’s Table 2 reveals the details:

Nutrient Current RDIs Proposed RDIs
Biotin 300 micrograms 30 micrograms.
Choline 5501milligrams 550 milligrams.
Folate 400 micrograms 400 micrograms DFE.
Niacin 20 milligrams 16 milligrams NE.
Pantothenic acid 10 milligrams 5 milligrams.
Riboflavin 1.7 milligrams 1.3 milligrams.
Thiamin 1.5 milligrams 1.2 milligrams.
Vitamin A 5,000 International Units 900 micrograms RAE.
Vitamin B 6 2.0 milligrams 1.7 milligrams.
Vitamin B 12 6 micrograms 2.4 micrograms.
Vitamin C 60 milligrams 90 milligrams.
Vitamin D 400 International Units 20 micrograms.
Vitamin E 30 International Units 15 milligrams.
Vitamin K 80 micrograms 120 micrograms.
Calcium 1,000 milligrams 1,300 milligrams.
Chloride 3,400 milligrams 2,300 milligrams.
Chromium 120 micrograms 35 micrograms.
Copper 2.0 milligrams 0.9 milligrams.
Iodine 150 micrograms 150 micrograms.
Iron 18 milligrams 18 milligrams.
Magnesium 400 milligrams 420 milligrams.
Manganese 2.0 milligrams 2.3 milligrams.
Molybdenum 75 micrograms 45 micrograms.
Phosphorus 1,000 milligrams 1,250 milligrams.
Potassium2 3,500 milligrams 4,700 milligrams.
Selenium 70 micrograms 55 micrograms.
Zinc 15 milligrams 11 milligrams.

As you can see, a few RDIs have actually been raised, such as those for Vitamin C, Calcium, and Magnesium.  In a few years, however, if the FDA has its way in implementing its Proposed Rulemaking, we can promise you that the FDA will work to conform the other Nutrient Values to those of Codex – either trying to force the Codex values up to FDA levels or else reducing FDA levels down to Codex ones.

You can find support for this promise by going back to at least the FDA’s October 11, 1995, pronouncement in the Federal Register, where the FDA made no secret of its intention and desire to harmonize its food laws with those of the rest of the World. This current Proposed Rulemaking with its label changes simply proves that this intention is still very much alive.

Were those Global standards for vitamins and minerals higher than our own, then such a change might be advisable, even admirable.  But we all know that most of the rest of the World despises supplementation, either separately or in foods, and since these proposed label changes for daily values apply equally to the Supplement Facts panel as they do to the Nutrition Facts panel, they are very dangerous changes indeed for the supplements that consumers rely upon.

There is a definite connection between these proposed daily values and maximum upper permitted levels, with harmonized global standards paving the way for overall reduced vitamin-and-mineral levels whether in pill form or food form.  This is my 15th year of actively following and arguing about dietary-supplement and general-food standards and guidelines at Codex meetings and I have seen the trend.  Believe me, the trend is not your friend, not here.

These Are Proposed Changes      

You will not see these changes right away.  First of all, they are proposed, not final. Secondly, the FDA is accepting comments from the public for a ninety-day period, which ends on June 2, 2014.  You should weigh in with your opinion, now.

We ask that everyone opposed to this Proposed Rulemaking send their comments electronically to the FDA at  http://www.regulations.gov/#!submitComment;D=FDA-2012-N-1210-0002 or in writing to the Division of Dockets Management (HFA-305), Food and Drug Administration, 5360 Fishers Lane, Rm. 1061, Rockville, Maryland 20852. Mention Docket No. FDA-2012-N-1210.

Feel free to use, and embellish upon, the following wording from here to paste into your e-comment on the FDA website: “On Docket No. FDA-2012-N-1210, I am adamantly opposed to your proposed reduction of vitamin-and-mineral Reference Daily Intakes as shown in your Table 2, on page 11931.  At a time when toxin intake is increasing and nutrient intake is decreasing, Americans need more vitamins and minerals on a daily basis, not less. Your unsupported goal of harmonizing our food laws to Codex standards and guidelines has been specifically prohibited by Congress, and I demand that you obey the law and immediately withdraw Table 2 and all supporting paragraphs of your Proposed Rulemaking for revision in line with modern nutritional science, which shows that we need a higher daily intake of  B and other vitamins as well as more magnesium and other minerals such as selenium.  Please act immediately to correct your serious errors.”

Keep in mind that even if the Proposed Rulemaking becomes final, food manufacturers will have two years to bring their labels into compliance with the final rule.  The FDA estimates that it will cost the industry approximately $2 billion to comply, but NHF has never known the government to be even remotely correct about the true and final costs of compliance.

The FDA has dressed up its anti-nutrient label changes with all manner of accessories. But don’t be fooled by the bling, for at the core lay the FDA’s ignorance about and antipathy towards the benefits of vitamins and minerals.  Tell the FDA exactly how you feel and how wrong it is.


[1] FDA News Release, “FDA proposes updates to Nutrition Facts label on food packages,”

February 27, 2014, at: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm387418.htm.

[2] See “Food Labeling: Revision of the Nutrition and Supplement Facts Labels,” 79 Federal Register 11879-11987, March 3, 2014, at: https://www.federalregister.gov/articles/2014/03/03/2014-04387/food-labeling-revision-of-the-nutrition-and-supplement-facts-labels.

[3] Scott Tips, “Living in the Past, Undermining Our Future,” Whole Foods Magazine, published earlier this month and posted online at: http://www.wholefoodsmagazine.com/columns/legal-tips/living-past-undermining-our-future; see also http://www.thenhf.com/article.php?id=3674

[4] 79 Federal Register, Table 2 at page 11931, which reveals all.


By Scott C. Tips

© 2014 Scott Tips

Scott C. Tips is President of the National Health Federation. Scott is a California-licensed attorney, specializing in food-and-drug law and trademark law, but also engages in business litigation, general business law, and nonprofit organizations, with an international clientele. Since 1989, Scott has been the General Counsel for the National Health Federation, the World’s oldest health-freedom organization for consumers, as well as the Editor In Chief of its magazine, Health Freedom News. In 2007, he became NHF President, and has been a frequent speaker for the organization and for health freedom on several continents. As legal columnist, Scott writes a monthly column for Whole Foods Magazine called “Legal Tips,” a column he started many years ago. Currently, he is primarily occupied with health-freedom issues arising from national governments’ and such international organizations as the Codex Alimentarius Commission’s attempts to limit individual freedom of choice in health matters. In that capacity, he has compiled, edited, and published a book on the subject entitled Codex Alimentarius – Global Food Imperialism. He also attends Codex meetings worldwide and has attended more Codex meetings than any other health-freedom activist.

Sen. Dick Durbin’s Dangerous Anti-Supplement Bill (TAKE ACTION)

Sen. Dick Durbin

The FDA can count on mainstream media to mislead the public. Let’s get the truth out and stop this bill. Action Alert!

Sen. Dick Durbin (D-IL)’s bill, S.1425, is meant to “improve the safety of dietary supplements by [requiring] manufacturers of dietary supplements to register dietary supplements with the Food and Drug Administration and to amend labeling requirements with respect to dietary supplements.” Sounds innocuous, doesn’t it? But as we reported in August, this is nothing but a smokescreen—a naked power grab for the FDA and an attempt to regulate safe dietary supplements as if they were dangerous FDA-approved prescription drugs.

A recent article in Newsday quotes “a top agency official” (probably FDA’s Division of Dietary Supplement Programs director Dan Fabricant, who is quoted extensively in the article) as saying that 70% of supplement companies have violated FDA’s manufacturing rules over the last five years—with the clear implication that such manufacturing violations somehow puts the American public at risk. There is no mention of the nature, context, or seriousness of these alleged violations, and no link to any official reports or documentation.

The article declares that the number of adverse events caused by supplements “outstrips” those triggered by prescriptions drugs. This is totally false. The Newsday article’s author, Delthia Ricks, tells us that approximately “6,300 people nationwide complained about adverse reactions to dietary supplements between 2008 and 2012, according to FDA statistics. But the actual number may be more than eight times higher, some experts say, because most people don’t believe health products can make them sick.” This “eight times higher” claim has no basis in fact, and no documented source. Even if it were true, this number is far less than for prescription drugs.

The 6,300 figure averages to 1,575 per year, which is extremely low considering that 157 million Americans—half the US population—take supplements. This is in comparison to 526,527 adverse events for prescription drugs, 275,421 of which had “serious outcomes,” including death.

Why would we want to let the agency regulate supplements as if they were drugs when the drugs they approve cause over 400 times the adverse events than supplements do? When the Government Accountability Office (GAO) looked at the number of adverse events for supplements at the request of Senator Durbin, it was unable to uncover anything alarming, as we reported back in March.

On the contrary, the GAO report showed that FDA-approved drugs caused 80% of Poison Control fatalities. More than 100,000 calls to Poison Control Centers, 56,000 emergency room visits, 2,600 hospitalizations, and nearly 500 deaths each year are attributed to acetaminophen (Tylenol) alone!

The Newsday article goes on to describe, in detail, the FDA’s authority to regulate the vitamin supplement industry, noting the agency’s inspection of supplement company facilities, and its ability to issue product warnings, recalls, and seizures and levy steep fines against companies that run afoul of FDA regulation. Inexplicably, the article then quotes Dan Fabricant as saying, “There is little the FDA can do to exercise more power over supplement safety without an act of Congress,” and concludes that FDA has “limited power” to regulate supplements. In what universe does that statement make sense?

The only way it makes sense is if mainstream media pieces like this Newsday article are viewed as propaganda: a concerted alliance between the media, the FDA, and legislators like Sen. Durbin to weaken the public’s determination to keep dietary supplements freely available. Lest this sound too conspiratorial, we need to remember that drug advertising is what keeps much of print media alive in these days of online competition.

The theme of adverse events is very much echoed in Durbin’s legislation. His bill requires that the FDA, together with the Institute of Medicine (IOM), compile a list of dietary ingredients (supplements) that might lead to adverse events, or are otherwise deemed risky in some way—based on completely arbitrary or nonexistent standards. Given the FDA’s profound bias against supplements, and the skewed, anti-science recommendations of the IOM’s vitamin D report, these are hardly trustworthy sources of guidance!

By the way, speaking of IOM and adverse events, why does the IOM absolutely refuse to study adverse events from vaccinations? In this case it holds that adverse events are meaningless because not studied, but then refuses to study them.

Returning to supplements, the FDA already has complete authority to keep them safe—it’s just a matter of enforcement, as the FDA’s Fabricant himself said when he worked for the Natural Products Association: “The barriers to enforcement are simple: [FDA] money, manpower, and will.” (You’ll note he doesn’t say “more regulation”!) He also made the distinction between the “legal, safe and healthy dietary supplement industry” and “the seedy, fly-by-night, unsafe world of illegal steroids,” and called on FDA, DEA, and other appropriate agencies to work together to enforce the laws that already exist. Most of the violations cited in the Newsday article are examples of bad manufacturing practices, which are already illegal and subject to FDA enforcement action. All the FDA has to do is enforce existing rules.

Another element in Durbin’s legislation is a greater restriction of health claims: he has said his bill is designed to stop “mislabeling products and making health claims that have no scientific basis.” This is more nonsense.

The vast majority of supplement health claims have plenty of scientific basis—just not the random-controlled trials (RCT) that Durbin and the FDA want. And there’s a very good reason for this: most natural products companies cannot afford to spend up to a billion dollars on RCTs, because in most cases that natural product can’t be patented, so the companies could never hope to make back their investment. In addition, many supplements should be taken with co-factors and so should not be studied in isolation like a drug.

Durbin knows all this. The demand for RCTs is just a backdoor way to get rid of most supplements entirely.

In the past, Dan Fabricant did not support greater restrictions of health claims. In response to IOM’s recommendation that dietary supplement health claims should be subject to the same scrutiny as pharmaceuticals, Fabricant said, “Trying to see foods through the same lens as isolated pharmaceuticals is impractical from a policy standpoint.” He also noted that many widely used general claims about how nutrients work, such as “calcium builds strong bones,” can’t be subjected to the same clinical evaluation as pharmaceutical drugs.

In other words, the FDA’s Fabricant said exactly what we’ve been claiming all along—that supplements are safe and the FDA needs no expanded powers—before he changed employers!

Action Alert! Please write to your senators immediately and tell them to stop Sen. Durbin’s frontal attack on your right to use supplements dead in its tracks! We don’t need this new legislation—all we need is for existing laws to be fully enforced. We need our access to nutritional supplements to be protected. Please write your senators today!


H/T: Alliance for Natural Health

UPDATE: Results of Codex Alimentarius Meetings 2012, In Frankfurt, Germany

codex alimentariusCodex Alimentarius is One Big Football Game

Codex Alimentarius is a UN-sponsored concept and organization, which – under the auspices of the World Health Organization (WHO) and the Food and Agriculture Organization (FAO) – creates food standards and guidelines used in international trade. In 1994, the World Trade Organization (WTO) replaced the General Agreement on Tariffs and Trade (GATT) with actual trade-sanction power to enforce Codex and other standards and guidelines. Not surprisingly, Codex took on an entirely new importance.

Now nearly 300 of us – Country delegates and International Non-governmental Organizations (INGOs http://en.wikipedia.org/wiki/International_nongovernmental_organization) – were involved in Germany this December in a playoff where inches of dry but crucial script would gain the yardage of victory or bitter defeat. This was the 34th session of the Codex Committee on Nutrition and Foods for Special Dietary Uses (CCNFSDU), alias “Malnutrition Meeting,” in frigid Bad Soden, Germany the first week of December 2012, where the National Health Federation sought to make its own gains and preserve our health freedoms.

In this innocuous meeting room at the Ramada Inn, play by play, line by line, either the “ball” is moving forward, backward, or it’s being passed or kicked into oblivion without regard to any real goal in a last-ditch effort to get rid of it before being tackled. In this case, for the majority of the represented World, ‘tackled’ was a voluntary fumble, “When is it break time? Let’s just agree with the provided wording and get a cup of coffee.” You have to realize the World doesn’t often enjoy what the United States takes completely for granted, in this case, safe, high-quality supplements in abundance.

In a worst case scenario, Codex is rigged and we merely delay the inevitable passage of their ultimate will. It takes a skillful operator – in this case Dr. Pia Noble (what a misnomer…) – who can lead the room and in clearly balanced opposition somehow convince or cow the country delegates into believing there is actually consensus. That’s how Codex operates: by consensus. We don’t vote unless pushed. The World must agree, must cooperate…however, what I witnessed at this session of the CCNFSDU was clearly, in legal terms, “leading” and manipulating the room to the wishes of three strong forces: the U.S., Australia, and, of course, Chairwoman Dr. Pia (anything but) Noble.

At Codex Alimentarius (Latin for “Food Code”), the plays are read, line by line, and debated on by a World that doesn’t necessarily even accept certain principles in their daily life – like taking supplements. As a Nutritional Therapist, this was my meeting. I had to be there. Thankfully a few staunch supporters made sure that happened.

In the case of this particular Codex meeting held in Bad Soden, the ball was in jeopardy of being punted into oblivion when we hit the discussion of Nutrient Reference Values (NRVs). Was there anyone out of the nearly 300 delegates who really cared at all about the issues that will impact you when you go to the health-food store this coming year? This was my second Codex meeting and I could see clearly that the paragraphs dedicated to the discussion of our NRVs were in danger of being accepted as written and set into stone around the World, all in favor of just getting to the coffee break, and I mean that literally.

You have to understand, United States citizens enjoy unprecedented access to supplements with values that actually have the power to prevent disease or heal ill health – the rest of the World either does not use supplements, believing they are toxic – like drugs – or the nutrient reference values (RDAs) are so low that multiple bottles would have to be purchased at great expense to create the impact that one good U.S. bottle creates, or they simply don’t have them because no one could afford them when their healthcare system provides “free” drugs as an alternative.

I saw the low reference values firsthand in Germany. We went into a health-food store and I could hardly find the vitamin/mineral section. I had to ask. When I did find the one small shelf, the highest values for Vitamin D3 were 400 IUs. I take 25,000 IUs daily…talk about breaking the bank. No wonder the World, represented in the form of country delegates, was anxious to get to the free coffee, sweet rolls, etc. at the break. Their countries cannot afford what seems to them to be nonsense, so they mentally have moved on and disregarded any pro-vitamin/mineral argument. This is not their World. In fact, if the National Health Federation were not present at this crucial meeting on setting Nutrient Reference Values, I can guarantee you that your World would never be the same again. Once lowered, do you really think NRVs would ever stand the chance of somehow going through Codex’s 8-step process to rise again?

From a Nutritional Therapist’s standpoint, several of the nutrients that were placed on Codex’s sacrificial altar were methylation factors. B6, B12, Folic Acid…If we don’t methylate well, we can develop opportunistic diseases. Cancer…heart attack that occurs when Homocysteine elevates…Some, like calcium, which Codex wished to elevate out of proportion to stabilizing magnesium, and when taken out of balance, creates disease as well by mineralizing in soft tissue like blood vessels instead of the bone and teeth. So, at this point I’m thinking, “Is Codex out to kill us?

So many of the final decisions made by Codex equal ill health for the World. It means both Big Pharma and the so-called “health” care system profits, while we grow ill and die. It is no secret that depopulation is one aspect of the World’s agenda. “Dr. Henry Kissinger himself wrote: “Depopulation should be the highest priority of U.S. foreign policy towards the Third World.” Apparently America is the new ‘third World.’

If you ever needed an advocate for your health and your health freedom, it is now. Now is the time to have your wishes and your Voice represented at Codex. Is it any wonder that Codex is not letting any more health-freedom organizations into the elite representation? The National Health Federation (NHF) is the ONLY health-freedom organization that has the power to speak out and, believe me, we do and we have – frequently. We have also submitted comments to the Electronic Working Groups that often meet in cyberspace before the meetings, and we also have the power to propose correction of the final report. Do you know how many delegates stick around for the tedious, line-by-line reading of the final report? Many are long gone, mistakenly trusting that the work they performed for the World will actually be represented accurately in the final report. NHF stays … to the bitter end. Hours of rehashing what we have spent the week working toward, defending our documented statements, defending the truth that too-often gets somehow skewed, omitted, or somehow rendered opaque.

NHF came to this meeting to promote and defend healthier Nutrient Reference Values. The attack by Australia and others on these particular NRVs, from my professional standpoint, is designed to take out a large number of the population at least in the U.S. where we have access to supplements with values that are currently at least approaching sufficiency and where we have the incomes generally to support their purchase.

What was so incredibly ironic about this meeting was the emphasis on malnutrition in the World. It actually sparked a growing interest in me about the integrity of infant formulas. They are including transfats and contaminants in infant formula! When we learn that in France, for example, breast feeding is neither popular nor widely practiced, it pays to defend the integrity of infant formulas! But the trajectory of the morning – 3 hours before NRVs were even approached – was on ‘growing up milk,’ which Elizabeth Streken (an INGO representative of the International Baby Formula Action Network) said was a market ploy to get mothers to feel guilty if they didn’t keep bottle feeding babies way past time… At any rate, the discrepancy and complete disconnect in regards to the NRVs was that supposedly Codex was there to prevent malnutrition in the World, yet here they were, the very last ones in favor of optimal nutrition for infants.  Instead, Codex was lowering our already malnutrition-promoting, low NRVs, which are set to prevent the very last-ditch disease processes before death instead of promoting optimum nutrition and vibrant, disease-resistant health.

So, these two themes predominated:  (1) Get through the tedious drivel and get me to the coffee and donut cart; and (2) The incongruous ‘Yes, we are all for stopping malnutrition … let’s lower the values in the supplements, shall we?”  And then let us not forget the overarching theme by Mme. Chair – “not so terribly Noble, Pia”— “What I Decide, Will Be.”

The National Health Federation has been in existence long before any other health-freedom organization was even a ‘gleam in the father’s eye.’ We are the granddaddy of them all. We’ve employed a lobbyist in Washington, D.C. for more than 50 years. We alone hold the distinction of being the only health-freedom organization able to speak at Codex. So, do you see now how important this ability is? Not only can we speak; but, as mentioned above, we can submit written comments and arguments – and we did, three times – on the NRV issue alone prior to the meeting in Germany (twice as part of the electronic working group hosted by the ultimate opposition: Australia, and once directly to the Committee).

Do I feel fortunate to be on the team of the most powerful health-freedom organization at Codex? I feel incredibly humbled. For one who had little political interest or influence in the past, I am now thrust into the heart of the action where policy is set for the World. It is not only quite humbling but it carries an enormous responsibility to carry the wishes and desires of those whom NHF speaks for and represents to the seat of power. And we do so faithfully time and again.

The lives that are impacted are not only our own but those of our children and grandchildren. Our family’s health is at stake. In the final analysis, if we lose our health, we have lost. It is all we have besides the faith that sustains us and keeps us seeking the path of Light in the growing darkness of the World. The Codex meeting on nutrition was anything but. It was about some elite marketers seeking to manipulate the World – guilting them into keeping children on formulas when they needed to embrace a solid diet – real ‘growing up’ food. It was about government regulators lowering key nutrients and raising others that would ensure that our health would deteriorate. It masqueraded in the guise of compassion and the oft-said mantra “consumer protection,” yet all the while was undermining our health by chipping away at the very foundations in the name of control and ill health.

We at NHF spoke for you. At the end of the day, I approached the dais where Dr. Pia Noble held court. I asked her for 5 minutes at the next meeting to explain the science behind our commitment to NRVs. She grimaced, rolled her eyes, disregarded me completely in the most disrespectful way possible for one woman to address another, and then deferred to the Secretariat. The answer was – you guessed it – NO. “It might create further discussion….”   Codex is a body that is supposed to elevate your health, not suppress it.  But who speaks for you there? The National Health Federation. That’s the real WHO.


By Kat Carroll, NTP,

Associate Editor, Health Freedom News, National Health Federation

To access NHF President Scott Tips’ article summarizing the Codex meeting, visit the website at www.thenhf.com or this direct link: http://www.thenhf.com/article.php?id=3567 or http://www.thesleuthjournal.com/codex-nutrition-committee-chooses-malnutrition/.  While you’re there, we invite you to join our efforts to protect the health of the World by becoming a member or helping to underwrite expenses to future Codex Alimentarius meetings like the one upcoming in March 2013 in Beijing where the topic of ‘contaminants’ will be reviewed. My personal passion is focusing on contaminants in infant formulas, as well as aspartame and aluminum in our food supply. We really cannot fight this fight without every one of you pitching in and doing your part. Believe me, it’s so satisfying to know we really ARE making an impact on this World for the benefit of future generations.