Archive for the ‘The Law & CODEX’ Category

Maryland Menaces Children, Parents Over Vaccination

Friday, November 16th, 2007

November 15, 2005

A Maryland Court has threatened thousands of children with imminent harm, and threatened to abrogate parental rights in a massive assault on both parents and children in Maryland.

In an article by Nelson Hernandez, a Washington Post Staff Writer, it was revealed that the State is attempting to coerce parents to expose their children to potential harm through its powers of intimidation and sanction.
This kind of intimidation to enhance State control of health decisions appears to be accelerating.
Only strong Health Freedom Advocacy will prevent the complete take over of our bodies.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation

Sign up for Health Freedom Alerts and take action to protect your rights now. www.HealthFreedomUSA.org

Wednesday, November 14, 2007; Page B01

The parents of more than 2,300 Prince George’s County students who failed to get needed vaccinations could face fines of $50 a day and up to 10 days in jail if their children do not meet the state’s immunization requirements, county officials said yesterday.
The threat of legal action is a last resort after months in which Prince George’s has struggled to get its 131,000 students immunized for chicken pox and hepatitis B, as mandated by the state. More than 2,300 students have not been immunized and have been barred from attending schools, almost two months after a Sept. 20 deadline for meeting the requirement.
“We can do this the easy way or the hard way, but it’s got to get done,” Prince George’s State’s Attorney Glenn F. Ivey (D) said at a news conference in Upper Marlboro. “I’m willing to move forward with legal action.”
School officials have made calls, sent letters and conducted home visits to make arrangements for free appointments for the needed shots. But often the students’ addresses and phone numbers have been outdated, making contacting them difficult. Other students have received the vaccines but failed to get the necessary booster shots.
The school system turned to the justice system as a final option and received the backing of Circuit Judge William D. Missouri, the county’s administrative judge, and Circuit Judge C. Philip Nichols Jr., who handles juvenile matters.
“This is an educational crisis,” said R. Owen Johnson Jr., chairman of the school board. “This is a public health and a children’s rights issue.”
Nichols and Ivey sent another round of letters to the families still out of compliance. Nichols’s letter ordered the parents to show up at Prince George’s Circuit Court for a court hearing and a free vaccine; Ivey’s letter warned that “unexcused absences by your child may subject you to a criminal charge.”
They expect almost 1,700 children to show up Saturday with their parents for the first in a series of Circuit Court hearings on the matter. School officials said the parents would receive a verbal reprimand from the judge and be ordered to have their children immunized in the courthouse. The students would then be allowed to return to school.
Parents who do not appear could face fines of $50 for each day they fail to get their children immunized after being charged. They also could serve up to 10 days in jail. Ivey said he hoped charging parents would not be necessary.

“The goal is to get kids in school, not to put parents in jail,” Ivey said.
Missouri said he looked forward to talking to the parents who had not gotten their children immunized, to understand why.
“I’d like to know exactly what the reasons are because the reasons may be able to be addressed without ratcheting it up to this point,” he said.

Schools officials said they were sorry the crisis had gone this far, but that it needed to be solved immediately.
“This has really, really been a difficult time for us,” said Betty Despenza-Green, the school system’s chief of student services. “It hurts us when any child is out of school because he needs to be immunized, and so we felt we needed to be creative. We need those students immunized. We need them in schools.”
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Letters, We Get Letters

Thursday, November 15th, 2007

November 15, 2007

Here are some of the letters we have been getting recently. They have not been edited but their authors’ names have been omitted. If you have a question or a comment you would like to share with the Natural Solutions Foundation, please feel free to send it along to the Natural Solutions Foundation at dr.laibow@gmail.com. We WILL answer you although it may take a little time since we are staffed by volunteers. If the matter is urgent, please say so in the subject line and we will give our email priority.

Thanks for writing! Keep those cards and letters coming!

Dr. Rima
Rima E. Laibow, MD
Natural Solutions Foundation
www.HealthFreedomUSA.orgwww.GlobalHealthFreedom.org

November 11, 2007
Dear Dr. Laibow:

I can tithe my time and feel this is very important-

I want to screen your videos for health professionals in the Body Mind field here in [writer’s home town]-

I am a licensed psychologist who works as an alternative healer/energetic therapist-
Our western health system is fascist and in shambles!

You are my hero! You go girl!
Contact me at [phone number redacted]
DM

I answered:

Dear DM:
Since I am in Germany at the Codex meeting calling you would be difficult BUT I am deeply grateful for your offer of help and your enthusiastic support.
I would be delighted if you would make sure that the professionals in your area are informed and, even more important, activated. You are quite right about our system and, since they are caught in the middle of it psychologically, culturally and personally, it is hard to see it until your eyes have been focused on the reality – and it is especially helpful if a peer assists in changing the cognitive framework.
I think the best place to start is a meeting with a brief introduction to the fact that the FDA is hell bent for leather on getting the economic competitors to drugs out of the way (giving people the opportunity to learn about the FDA Cam Guidance which will allow the FDA to define CAM as MEDICINE, thereby making the practice of natural techniques the province of licensed physicians ONLY, then discussing the other threats (what is your State doing to support or attack your activities?) and then an introduction to the Codex would be a pretty dense information flow for the first meeting. What should emerge from that is a determination to
1. learn more – please have our website available for people to go to:
2. do more – if people are energized to spread the word to colleagues and patients they can become a positive and effective force for protecting mind body practices
3. arrange another meeting with colleagues, patients, friends, etc. At that meeting, a screening of my nutricide lecture (available on “Nutricide: the DVD” , a discussion of the implications of the Codex process (including HARMonization) and how it fits into the US suppression of natural health, gathering signatures on the legal challenge to HARMonization, the Citizens Petition, having a computer available in the room so that people can go to our site and sign up for the Health Freedom Alert (and make donations to our Foundation if they are so inclined) right there and a group decision on the next steps for your community would be a great “two step process” all on its own.
Please contact Kathy Greene to let her know that you would like an organizer’s kit. And stay in close touch!
Thanks for your support!
Yours in health and freedom,
Dr. Rima

Dear Dr. Laibow:
This [Codex threat] sounds like a worthwhile message, but I don’t really understand it.
> Can you, perhaps, explain it in terms that are simpler and more direct
> — and without quite so much detail?
WD

and we answered:

Dear WD:
Your email to Dr. Laibow was sent to me for response. Thank you for taking the
time to communicate.

Now, how can we make the message simpler?

In common law countries like the US, you are free to do whatever is not
specifically forbidden by law. In “code” countries, like most EU countries,
you can only do what is permitted by law.

Codex Alimentarius – the World Food Code – arose from part of the Napoleonic
Code and with its various approved lists and guidelines attempts to control
all foods, including supplements. It goes even further, though, led by a
chairman who has a personal interest in a “risk analysis” company in Germany.
Codex wants to treat supplements as though they were industrial toxins,
subjecting them to a “risk analysis” that would forbid all that have a
demonstrable impact (for good or ill). Without considering bio-individuality.
At the same time, of course, no such analysis is required for genetically
modified or irradiated foods or drugs (drugs are allowed to have “risks”

If you want to remain free to control your own food and healthcare, we need
your help. It’s that simple.

For Natural Solutions,

Ralph Fucetola, JD, Trustee
The Vitamin Lawyer.com Consultancy
http://www.vitaminlawyer.com
http://vitaminlawyerhealthfreedom.blogspot.com
All Rights Reserved . . .

November 11,2007:

Dear Dr. Laibow:
Thank you very much for the update on what is going on regarding the attempted implementation of Codex Alimentarius. It has been an on-going battle to stave off the loss of our health freedoms ever since CODEX was adopted in the U.N. in the early 1960’s. Under the guise of uniform standards for all nations of the world for health and nutritional products, CODEX actually is designed to make it very difficult and expensive for the average person to have affordable access to herbs, vitamins, nutritional supplements and other health promoting products. The more people become healthy and don’t need pharmaceutical drugs, the less money the drug companies can make. It’s all about money. If we are all sick and have long-term degenerative diseases and are all on drugs, what a financial boon for big Pharma. Lately, the FDA has been trying to even prevent information from being published and distributed about historic and traditional benefits that have been known for centuries regarding natural herbs and other natural therapies and supplements. People should not be taking this sort of thing lightly but rather should be alarmed. The FDA has lost sight of it’s true purpose of keeping food & medicine safe and have instead become the pawn of the drug companies to squelch competition from the natural health sector so Big Pharma can have ALL the Pie. Luckily, more and more people are waking up to what is going on and are willing to do something about it like you have been. Thank you! Your efforts are very much appreciated! On Nov 11, 2007 10:16 PM, Vicki Knapp wrote:
Dear Dr. Laibow: Thank you very much for the update on what is going on regarding the attempted implementation of Codex Alimentarius. It has been an on-going battle to stave off the loss of our health freedoms ever since CODEX was adopted in the U.N. in the early 1960’s. Under the guise of uniform standards for all nations of the world for health and nutritional products, CODEX actually is designed to make it very difficult and expensive for the average person to have affordable access to herbs, vitamins, nutritional supplements and other health promoting products. The more people become healthy and don’t need pharmaceutical drugs, the less money the drug companies can make. It’s all about money. If we are all sick and have long-term degenerative diseases and are all on drugs, what a financial boon for big Pharma. Lately, the FDA has been trying to even prevent information from being published and distributed about historic and traditional benefits that have been known for centuries regarding natural herbs and other natural therapies and supplements. People should not be taking this sort of thing lightly but rather should be alarmed. The FDA has lost sight of it’s true purpose of keeping food & medicine safe and have instead become the pawn of the drug companies to squelch competition from the natural health sector so Big Pharma can have ALL the Pie. Luckily, more and more people are waking up to what is going on and are willing to do something about it like you have been. Thank you! Your efforts are very much appreciated! VK

We responded:

Dear VK:
And Thank YOU! Our effectiveness is in the fact that our associates (those on our email list) are wonderful, decent people who have a dream of what America can become again! They know that our health freedoms are an important part of that dream! Every time we ask that people send out messages to Congress, Wash DC gets blasted with tens of thousands of emails- much more than they are used to getting- and they know that our group is WATCHING!! The grassroots groups are growing and spreading the word, and hopefully, soon, we will be able to get millions of emails to Wash DC. Dr. Rima has tremendous energy! (It helps to be wearing skates if you are with her when she is lobbying in Congress!) So keep spreading the word, and if people are interested, get us their email addresses so we can keep them up to date, and stay focussed on that future we all hope to see!
Kathy Greene for Dr. Rima Laibow

November 11, 2007

Dear Dr. Rima:
First, I want to thank you for your dedicated work to fighting for
Health Freedom. I read most of your report about how “the team”
seems to be back sliding. What infuriates me is the fact that ANY
foreign regulation will attempt to control the nutrient
quality/quantity of our foods and supplements. Any attempt will
prove along the lines of genocide. Believe me, God in heaven will
call on those who will be awakened and this WILL be resisted and
overcome. He has had you fight this good fight, but please be
assured that you are not alone in this. His unconditional and
everlasting LOVE will sustain you and provide you with the relief you
will need when you think you just may be utterly alone. You are not
alone, Dr. Rima, and I felt led to just let you know this. Hang in
there, we are here fighting along side of you even if we are just in
the shadows. God Bless!
FF

We responded:

Hi FF!
What a nice letter! And yes, Dr. Rima has been doing a marvelous job of leading this crusade for health freedom! But our effectiveness is in our numbers and that includes people like YOU who happily send those thens of thousands of emails to Congress making the Powers that Be aware that we are all WATCHING! So keep spreading the news about Codex, et als., and when you meet people who wish to know more, get us their email addresses so that we can keep them up to date and so that we are soon sending MILLIONS of messages to Wash DC. That’ll keep em in line!!!!
Kathy Greene for Dr. Rima Laibow

Date: Nov 11, 2007 9:10 PM

Dr. PR sent a copy of a letter to another health freedom organization with two questions for them. We are glad he shared them with us, too:
Dear Sir/Ms:

1) As a member of the [another health freedom group], before I forward [Natural Solutions Foundation’s] email to my Distribution List, I kindly request that you comment on it and on one of its links:

Here in Codex Land: Codex Report No. 3, Nov. 11, 2007

2) The only person I ever hear from about what’s going on at the Codex nutrition deliberations is Dr. Laibow. Why don’t I ever hear from the [other organization] about what’s going on at the Codex nutrition deliberations?

Sincerely yours,

PR, PhD

We answered:
Thanks for letting us know about your questions. The reason you hear from the Natural Solutions Foundation when we attend Codex meetings is that we know that every one can’t be here, but everyone needs to know what is happening at Codex since it impacts us all so strongly.
Yours in health and freedom,
Dr. Rima

we responded:

This same correspondent started his communication to us this way:

Dear Dr. Laibow:

Asking Health Freedom supporters to send petitions to Schneeman is doing them a great disservice – it makes them think that they are doing something useful. It’s like asking asking civilized people to send a petition to Hitler to shut down the extermination camps and making them think that such actions would be helpful to his victims. Schneeman is a bureaucratic lowlife and nutritional Neanderthal who has done everything possible in her power to subvert nutritional freedom. It’s incredibly naive, even self-destructive, on your part to think she would be amenable to ANY number of petitions from health freedom supporters – they end up in her wastebasket as fast as they arrive. YOU ARE DIVERTING PRECIOUS CITIZENRY RESOURCES FROM MUCH MORE USEFUL ACTIONS, such as petitions to CONGRESSMEN asking them to clamp down on her criminal Codex actions on behalf of Big Pharma. Unless you change your petition approach to a more productive direction, I will reluctantly conclude that your
Health Freedom efforts will likely come to naught.

Sincerely yours,

PR, PhD

to which we replied:

Dear Dr. R.,
You have totally missed the point of the Citizens Petition, I am afraid. We are not petitioning Schneeman, nor are we petitioning Scarbrough. We are using our First Amendment Right to Petition for Redress to institute a legal challenge to the illegal “Harmonization” with Codex being carried out by the FDA. The process that we are involved in right now is called “Exhausting our administrative remedies” and renders the case, as they say in law, “Ripe” for further action.
So I beg to differ with you and actually wonder why you did not think to ask about the reason we have chosen this action before blasting us for not doing it in a way that made sense to you. Our health freedom actions are, in fact, well conceived and carefully planned with lawyers and expert strategists. No one is perfect and we could be making a mistake but, in fact, we are not.
Thanks for your input and your passion, though. I hope that you will continue to use it as a supporter of what we, alone among other health freedom organizations, are doing: solving the problem on multiple fronts.

Yours in health and freedom,
Dr. Rima

Hand Luggage on the QEII- Codex Report No. 4

Tuesday, November 13th, 2007

November 13, 2007

Today was a day like any other day at a Codex meeting: boring, stultifying, mind numbing and filled with tiny treasures of reality amidst a sea of obfuscation. As I have said so many times, the great majority of the people who come to these meetings are the bamboozled, not the bamboozlers. They come with a variety of expectations and beliefs about the process, but they are not interested in subverting either reality, health or freedom as far as General Stubblebine and I can make out. As the words flow on and on and on and on, though, if you listen carefully enough you will hear the subtext which comprises the reality of Codex. And then, when you point these underpinnings of reality out to people who actually sat in the room as they flew by, the reaction is really quite interesting: a lot like the stages of dying: denial, shock, depression, anger, and, unlike dying, a determination to change the outcome, at least in the home country of the person processing the newly identified reality. I had the opportunity to speak at length with two members of the supplement industry (who had no clue that Codex was working pretty hard to put them out of business but began to “grok” it pretty hard and fast as we talked over dinner) and five African and 2 Asian delegates who, likewise, were not clear about Codex’s agenda before our talk, but see it rather differently now.

In fact, an African delegate whom I had met several times before at Codex and her home country came up to me today and said that she was shocked that everything that Codex was doing was fine with me. Now it was my turn to be shocked and I asked her what she was talking about. She explained that she knows me to be very vocal and forthright but I had made no comments during the meeting. I told her that the Natural Solutions Foundation is a Public Observer (no opportunity to speak during the meetings) but that I most assuredly did not agree with what Codex was doing. Then she did something extraordinary: she asked me if I would please make sure to email her a month or so before the Codex meetings and tell her what the Natural Solutions Foundation positions and concerns were so that she could give them language during the meetings! This African government official wants our input so that our concerns can be the concerns of her country in the dialogue of Codex! Being there is half the fun. Speaking there is the other half of the fun and this delegate volunteered to have half the fun for us!

What happened today? Some other amazing things, in addition to the one!

A few examples: The standard for gluten free foods has been dragging on and on and on and on. For years and years and years.
I mentioned that in the full day workshop on the topic (Saturday, November 10, 2007) the debate ranged hot and heavy between the “not one part per million more than 20 ppm of gluten as the absolute upper standard for a gluten-free product” and the “well, we’ve been selling gluten-free foods up to 100 ppm (and the 1981 Codex standard allows 200 ppm) for years so what’s the big deal with allowing 100 ppm as the gluten-free standard” teams. YEARS! Back and forth, days and days, papers and more papers, working groups and electronic letters and on and on and on.

Today, somebody let the cat out of the bag. The Great Gluten Food Fight was a meaningless struggle that had absorbed well over a decade of time and effort. In exasperation, Dr. Rolf Grossklaus, Chairman of the Codex Committee on Nutrition and Foods for Special Dietary Uses (CCNFSDU) finally uttered the truth. Here is a verbatim report of his remarks: “Whether it is 20 or 100 ppm, these are trace elements and do not put the patient at risk.”

In other words, these meaningless struggles which have been going on for well over a decade are useful because they absorb energy and time, diverting attention and awareness from the real agenda of Codex. By numbing the mind, distorting and fragmenting the process of dialogue and agreement, enmities and allegiances are created which are then skillfully exploited to cement total control of the process while a feeling of compliance and [pseudo] accomplishment is allowed to pass for real forward movement on real food safety and security.

Responding to that comment, the Association of European Coeliac Societies (AOECS) said, “To put things in the right situation, we are talking about hand luggage on the biggest ship in the world: the Queen Elizabeth. You are talking about how many pieces of hand luggage you want to put on the world’s biggest ship.” This meeting has been rich in people doing small, irrelevant things on huge ocean liners. This is not a meeting of one liners! (Joke).

The amount of energy which this standard has absorbed is astonishing but makes sense viewed from the perspective I outlined above. That is not to say that reliable labeling for “gluten free” (or “reduced gluten” or “low gluten”) are unimportant. But 14 years? Come now!

Another example: Health Claims. If you make it impossible to let people know what nutrients and foods can do for them, then they will be far, far less likely to use them for a health benefit. That is the game the FDA is playing in the US and they have made sure the game extends to Codex as well. The US attends all of the Codex Committees (as you would expect, after all) so it can tie together efforts to achieve something in one of them with the same agenda in other committees.

As you may recall, we reported from the Codex Committee on Food Labeling (Ottawa, May, 2007) that the US (of course) had tried to bull through (assisted by the usual cast of culprits: Canada, Mexico, Australia, New Zealand and the EU) a definition of advertising which said that ANY communication which linked a health benefit to a food or food component which resulted in a change in the consumer’s beliefs, behaviors or buying patterns around food was to be considered advertising. We provided enough information on that absurd guideline that a number of countries took exception to it and academic publications without no commercial interest in the food were exempted. But what your friend says to you over the water cooler or what your doctor (or mother) tells you is still “advertising” and can expose the “advertiser” to legal action by the FTC, FDA or their legal lackies.

Here in the US, both the FDA and the Federal Trade Commission could jump all over anyone who provided such information – anyone. That would include scientists who published papers on food and health, journalists, doctors, mothers, health food store clerks, anyone at all. Through selective enforcement, plus some mainstream propaganda, suppressing that competitive information could get even easier for the drug folks.

Since the FDA (whose Dr. Barbara Schneeman so ably represented industry interests in her position as US Delegate at that meeting) had worked on that Codex Guideline for several years, it is, in our opinion, no surprise that they were already positioning the US for implementation of restrictions on truthful information about the health benefits of food (the single most significant competitor to drugs and drug profits) and took actions like the following:
December 2006: FDA issues Draft Guidance on CAM Regulation for Industry which states that products used with a health intent may be declared untested [hence, illegal] devices or drugs. Information used to convey that health benefit and intent to gain it thus become a force in moving foods into the category of untested drugs since it creates the expectation of a health benefit when using the food or food component.
March 2007: the Michigan Cherry Growers post several independent scientific papers stating that cherry juice is good for people with arthritis. FDA orders them to remove the papers and all references to them or they will declare cherries an untested drug and thus ban them in the US.
July, 2007 FDA issues Draft Guidance on Health Claims which says that “significant scientific agreement”, an impossible and totally unnecessary standard for safe, effective and long-used supplements (no new ones are allowed on the market which were not in use by June, 1994 unless they undergo extensive testing). By confusing information (like the cherry juice studies) with health claims, true speech is being stifled. Truthful statements about health benefits would be illegal and subject to FDA enforcement.
March, 2007 Ron Paul (R-TX) introduces Health Freedom Protection Act, HR 2117, to assure Americans the right to make, and learn about, truthful health claims which are supported by scientific evidence. (Evidence-Based Review System for the Scientific
Evaluation of Health Claims
)

June, 2007 FDA introduces Good Manufacturing Practice for supplements which, by its own economic impact analysis, will drive most small and many medium size nutrient companies because of burdensome requirements. Nutrients are safe and effective. Virtually no nutrient-related deaths have ever been reported.
November, 2007 US, represented by FDA employee Barbara Schneeman, PhD, head of FDA Office of Dietary Supplements, supports CCNFSDU Health Claims document which the US comments on saying a Health Claim is any representation that states, implies that a relationship exists between a food or a constituent of that food and health” and that such claims must meet absurdly high scientific agreement standards.

Is this a plot? No it is a plan. Remember, when I used the term “Nutricide” I gave it 2 definitions. The first one is “the death of the body of knowledge relating health benefits and food”. For the second one, go here (http://www.healthfreedomusa.org/index.php) and click on the featured video.

Can’t get enough of Codex: Special bonus: If you want to read a near-real time account of some of today’s Codex session and its implication, click here (http://vitaminlawyerhealthfreedom.blogspot.com/2007/11/notes-skyped-from-codex-by-dr-laibow.html).

Being here means that you get the straight story – every time! No cushions on the deck chairs being rearranged, just clear analysis and straight information. Our support comes from you and you alone. Click here (http://www.healthfreedomusa.org/index.php?page_id=189) to make a recurring donation (tax deductible, of course) to keep us afloat and fighting. Thanks!

Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation

Friends Don’t Let Friends Eat GM Cake -Codex Report No. 4

Tuesday, November 13th, 2007

November 12, 2007

Today was the first full day of work for the good men and women who attend the Codex Committee on Nutrition and Foods for Special Dietary Uses (CCNFSDU) and they are, at least for the most part, hard working, honest people who have been bamboozled.

The Report (from the Ad Hoc Committee on Foods Derived from Biotechnology about genetically modified (GM) plants which have been modified to produce nutrient(s) or related substance(s)) that we are reviewing right now in the Codex meeting is very, very interesting and very, very disturbing — but may ultimately be quite useful in the US and elsewhere. For example, although the US, via the FDA, has declared administratively, not scientifically, and in the absence of any testing to determine the truth of its position (or the safety of genetically modified [GM] foods) that GM foods and natural foods are equivalent and GM foods are safe. They refuse to do any safety testing to back up this dangerous – and potentially lethal – assertion. My assumption, of course, is that testing is the last thing they would want because it would show how very dangerous GM food actually are.

In this Report, curiously specific to “foods modified for nutritional or health benefits”, it is clearly stated in Section 1.1 that this document “does not cover assessment of the benefits themselves” but (Section 1.2) “the [GM] trait is a result of i) introduction of a new nutrient(s) or related substance(s), or ii) alteration of either the quantity or bioavailability of a nutrient(s) or related substance(s), iii) removal or reduction of undesirable substance(s) (e.g., allergens or toxicants), or iv) alteration of the interaction(s) of nutritional or health relevance of these substances.” Whew! Sounds like we could do with a little “assessment of the benefits themselves” before we go messing with the food and nutrient supply.

Oh, yes, for those of you in the US or eating US foods and taking US nutrients: under US law, it is not legal to introduce a new or novel Dietary Ingredient which was not in use before June, 1994 without extensive testing. Whoops! The US Delegate, Dr. Barbara Schneeman (FDA head of Office of Dietary Supplements). did not think fit to mention that, therefore, this Codex provision violates US law in several ways and so cannot be subject to FDA’s announced penchant for “HARMonized” regulations. So unsafe/untested foods could then be marketed in the US which violate US law because they introduce novel nutrients, although the benefit of doing so has not been evaluated or studied. Yummy! Sounds like food safety to me. NOT! So if the US “HARMonizes” with this standard, as it has said it will do, illegal foods could be marketed in the US with the knowing acquiescence of the US FDA!

Next in the list of Wonder Words produced for the “Guidance of the world community” is the following (Section 3.6) “Foods derived from recombinant-DNA plants modified for nutritional or health benefits may benefit certain populations/sub populations, while other populations/sub populations may be at risk from the same food.

Hang on there! The US FDA assures us that all GM foods are exactly identical to their non GM counterparts. Exactly. There is no difference whatsoever. So how can some populations be at risk from them? In fact, in a statement taken from the FDA website, we read, “The 1992 policy is based on existing food law, and requires that genetically engineered [GM – REL] foods meet the same rigorous safety standards as is required of all other foods. The law places a responsibility on producers and sellers to offer only safe products to consumers, and provides FDA with the legal tools for enforcement.” It is worth asking, though, if the FDA forbids the labeling of GM foods (except raw produce which carries a little oval tag with an identification number starting with the number 8) how such enforcement could be carried out when traceability, and therefore liability, is totally impossible if the food is not labeled with the strain of GM foods it contains. Do you feel safe yet?

But back to the issue at hand: if Codex acknowledges that these GM foods ARE different and the US says they are not, what happens next? Can the US use its might to force a change at the Codex Commission level? We shall see. Can the World Trade Organization force the US to identify those foods which are GM because Codex says that they are different? Can the US policy of refusing to label GM foods be challenged in court? In the World Court? In the World Trade Organization? Through a Consumer-initiated class action suit?

Moving right along, Section 3.7 notes “Rather than trying to identify every hazard associated with a particular food,…

[Hazard? Maybe foods should have upper dose limits assessed through Risk Assessment: for example, “That’s one too many Brussels sprouts, my fine young bucko! Risk assessment shows that the sulfur contained in 6 sprouts can help detoxify mercury stored in the brain – that could be a risk because you might not be able to get rid of that mercury floating around so you can only eat 5 of them!” REL]

… the intention of a safety assessment of food derived from recombinant-DNA plants is the identification of new or altered hazards relative to the conventional counterpart….

[Now hang on there once again: the US FDA, which we all know is working in our best interests, not for the good of industry, right? {after all, Dr. Schneeman personally told me on Saturday that it should be the goal of the FDA to protect the consumer} says that there ARE no risks and hazards associated with GM food. IF there were, FDA could not approve GM foods as if they were identical to foods that have not been modified. Yet Codex is saying that there may be new or altered hazards in GM foods compared to natural foods. What’s wrong here? Has reality, coming from the unlikely source of a Codex Report, come face to face with administrative fantasy engaged in by the FDA for the benefit of the Biotech industry? Imagine that! ]

The paragraph goes on to state, “Since recombinant-DNA plants modified for nutritional or health benefits
[assumed, not established, as pointed out before -REL] result in food products with a composition that may be significantly different from their conventional counterparts [sorry to break in again, but what did we just hear? “May be significantly different from their conventional counterparts”? But the FDA says it has already decided, without the science to back it up, that GM foods are NOT significantly different from their counterparts and, for that reason GM FOODS MAY NOT BE LABELED AS SUCH IN THE US SINCE CONSUMERS WOULD MAKE THE “MISTAKE” OF REJECTING GM FOODS IF THEY KNEW THAT THEY WERE GM FOODS. It doesn’t sound like such a mistake to me when you read that Codex says that they may be significantly different and may have hazards that regular foods don’t.]

Moving right along, “the choice of an appropriate comparator is of great importance for the safety assessment addressed in this Annex [the US, of course, says that no safety assessment is needed since GM foods are the same as non GM foods so the concept of a “comparator has no meaning if you accept the US position. REL]. Those alterations identified in a plant modified to obtain nutritional or health benefits are the subject of this safety assessment.” [So these plants need safety assessment in Europe, Asia, Africa, South America, but not the US. OK. Got it! REL]

But if that were not quite bad enough, consider this little bit of madness: Section 3.11 says, “With conventional fortification of food, typically a nutrient or a related substance is added at controlled concentrations and its chemical form is characterized. Levels of plant nutrients or related substances may vary in both conventionally bred and recombinant-DNA plants due to growing conditions. In addition, more than one chemical form of the nutrient might be expressed in the food as a result of the [genetic] modification and these may not be characterized from a nutritional perspective.” [Emphasis added – REL]

Whoa! So unknown versions of the chemicals we call nutrients could be produced and we are supposed to eat them? Just like we are supposed to use patentable but dangerous hormones which science has shown to cause cancer, stroke, blood clots, Alzheimer’s Disease, Heart Disease and high profits for the owners of the patents instead of low profit, un-patentable bio-identical hormones which are not associated with these disease states? In a biologically active compound, a change in a single molecule can mean the difference between toxic/deadly and nutritional/health promoting. These GM plants are producing God-knows-what version of what might be a nutrient and might be a poison and we are supposed to eat it and feed it to our children? Are you still feeling safe?

The report continues, “Where appropriate, information may be needed on the different chemical forms of the nutrient(s) or related substance(s) expressed in the portion of the plant intended for food use and their respective levels.” MAY be needed? Well, yes, I rather tend to think so, don’t you? There are unknown hazards from eating chemicals that have never before been produced on this planet and it MAY be advisable or appropriate to get some information on them? Of course, the FDA doesn’t think so. How safe should we feel?

Section 3. 12 makes the point that the bioavailability of these “nutrients” should be established. A good point, because modified substances may not have any nutrient value or may be downright toxic. Who knows? Not even the Shadow knows! Yet the item says that that bioavailability should be established, where appropriate as if it might not be an absolute necessity! My safety meter is pegging out. How about yours?

But wait! There’s more!
Section 3.13 makes the point that that animal testing is nearly meaningless so the “nutrients and related substance” [that could easily mean a toxic compound, or a whole uncharacterized stew of them] are best tested in human beings to determine “to what extent the nutrient or related substance is bio-available”. So let’s use humans to see if they develop deficiency diseases because the “nutrient” turns out to be non bio-available or develop toxic reactions (perhaps, say, cancer, death, etc.), shall we, because the modified substance may be bio-available, but it may be a bio-available toxin. This is contrary to the Declaration of Helsinki on Medical Experimentation. (http://www.wma.net/e/ethicsunit/helsinki.htm)

Interestingly, Section 3. 14 notes “When evaluating exposure, it is appropriate to consider information on whether the consumption of the modified food could lead to adverse nutritional effects…,” Right. I think that’s appropriate, too. The FDA, of course, does not. But another interesting question is, from where is that exposure data supposed to come?

Thailand picked up on this serious problem: human experimentation to evaluate dangerous hazards of the GM foods. He said that he was sure that the necessity to test these GM foods on humans was an error and that they should be tested on animals. It was at that point that the German Secretariat interrupted and stated that the only option CCNFSDU had was to approve the report. And some tell us we are “alarmist” when we seen a totalitarian agenda behind Codex! Like a child, the nature of the parents impacts Codex. Click here (http://video.google.com/videoplay?docid=-5266884912495233634&q=Nutricide&total=12&start=0&num=10&so=0&type=search&plindex=0) for more detail on those totalitarian roots.

Yesterday, I took the organization with Observer Status at Codex which identifies itself as pro-health freedom to severe task because instead of protesting the dangerous (and illegal in the US) Codex policies of nutrient risk assessment, they were, as I put it, “rearranging the cushions on the Titanic’s deck chairs”. Someone characterized this assessment as “a mindless attack”. It was, in fact, quite seriously mindful of the dangerous tactics taken by Codex and the failure of this group to speak out against them. When a health freedom organization fails to speak out for health freedom (despite a later press release to the contrary), it should expect to be taken to task for that failure. That way, it can improve its representation and participation. Hopefully, we all learn from criticism. We appreciate constructive criticism and it was in that spirit that we told you what we observed (and what did not happen !) at the meeting.

But today, one of the members of that organization did, in fact, ask a good question. He did not make the rest of the point (that this is an atrocity and must not be perpetrated on consumers) but he did ask the following question of the CCNFSDU plenary session: “Since”, he said, “95% of the consumers of the European Union and millions of others do not want to eat Genetically Modified foods, where will you get the exposure data to tell you whether there is exposure to unintended components?”

Dr. Grossklaus answered, “If you have a PKU person [who cannot ingest a specific amino acid without major damage – REL] and you make a Phenylalanine-free [the specific amino acid they cannot tolerate – REL] maize [corn – REL], then people will see that it is a good thing and they will eventually change their minds”.

People with Dr. Grossklaus’ degree of arrogance often make the most blatant statements which make clear exactly what they mean while other, more cautious, people would forebear. This was one of those moments. In essence, Dr. Grossklaus said, “Let them eat Genetically Modified Cake! They’ll learn to like it!” And it’s risky cake, as even Codex makes clear!

So, in addition to asking a philosophically interesting question, I was appreciative that the organizations representative asked a question that smoked out a clearly stated statement from one of the primary Codex manipulators. When a person or organization does something that I think deserves commendation, I will commend it.

And so it continues…

Yours in health and freedom,

Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org

PS – Perhaps even more telling, when I expressed my concern to Dr. Grossklaus over the cast he was wearing on his leg and asked if he was taking certain nutrients (that accelerate the healing process) he admitted he was… but they are forbidden by the European Food Supplements Directive! Ach! such a good nutritional doctor. REL

Here in Codex Land: Codex Report No. 3, Nov. 11, 2007

Sunday, November 11th, 2007

The rules here in Codex land are different from the ones that you and I know.
As you may know, Gen. Stubblebine and I are attending a Codex committee meeting in Germany. In our world, yours and mine, food should be clean and government agencies charged with protecting public health should prevent dangerous toxins from reaching our food or air, soil and water. But here in Codex-land, just the opposite seems to be true. Dangerous/profitable toxins of every sort are enthusiastically permitted into food and the environment EXCEPT for those alleged “toxins” which have a beneficial impact on health. In Codex-land, nutrients have to be controlled rigidly and kept at minimum levels, barely sustaining life but compromising health. That way, the preventable diseases of maximum profit caused by under nutrition can take root and flourish. You know what those diseases are; Codex’ parent UN agencies, the WHO and FAO have listed them: cancer, diabetes, heart disease…

As bizarre as it seems to us, all nutrients are treated as toxins here in Codex-land. So far, the Vitamin and Mineral Guideline doing so has been ratified, but the plan, articulated well today during the Codex session, is to treat all nutrients the same way: as toxins. But the one “health federation” group accorded “Official Observer” status does not get what is going on
Since natural therapies and health options (including herbs) are to be eliminated through Risk Assessment, the only legal strategies left to treat these preventable diseases of under nutrition will be … drugs! Considering the provable history of Codex as a drug industry idea, that makes pretty good sense, at least from their viewpoint!

Sunday was a fascinating (and troubling) day here in Codex-land. There was no amplification for the meeting (although it was an announced Working Group, just like yesterday’s session on Gluten-Free Foods for which amplification was provided) and the room where the meeting took place was full of reverberations making it very hard to hear (and making my verbatim note taking really challenging). There were hardly enough seats for everyone although the group was small so we were crowded together in a very big room nor were outlets provided as they usually are. That made electronic note-taking difficult unless you found a wall socket and plugged your computer in creating a hazard in the walkway. That’s what I did. I figured that my minor hazard was nothing compared to the global one they were creating in the meeting.

Dr. Rolf Grossklaus, Chair of CCNFSDU (Codex Committee on Nutrition and Foods for Special Dietary Uses), supported by the European Union and the United States, of course, has been enthusiastically flogging the notion that nutrients should be treated like toxins for a very long time, since about 1995, in fact. (The fact that he runs a Risk Assessment company has nothing to do with his position on the issue, right?)

Today it became clear that everyone in the room, including those people who might well be expected to be on our team – the health freedom team – had succumbed to the lure of the group mind. The health freedom team was nowhere to be seen intellectually although a “health federation” which is an Official Observer (and can thus speak in the meetings) was actually physically present. Natural Solutions Foundation – as an NGO (nongovernmental) public observe – was relegated to the balcony – and has not been granted Official Observer status since, we were told, the Codex observer rule says that groups with similar interests are supposed to work together and, says Codex, such a group already has “status.” We have not, I am saddened to state, ever been invited to participate in the “official” health federation group, although, for example, industry groups are regularly allowed to participate in the official US delegation.

Well, the official health federation delegates’ contributions were dismally disappointing. Instead of representing the voice of reason and health freedom, neither the lawyer nor the scientist representing this group took the least exception to the idea that nutrients SHOULD be regulated as if they were dangerous. Instead, they spoke in favor of using ranges of permitted doses between the necessary minimum and the permitted upper limit of a nutrient instead of hard and fast numbers.

Let me ask you, WHAT upper limit?

Under US law there can be no upper limit set.

Because of biochemical individuality there can be no upper limit set.

When nutrients are used to restore lost health, mega doses may be needed on an individualized basis so there can be no upper limit set.

Nutrients are foods and, as such, generally regarded as safe so there can be no upper limit set.

But, first and foremost, we in the US are protected by DSHEA*, the 1994 law which says that there can be no upper limits set on nutrients are foods and, as such, generally regarded as safe so there can be no upper limit set.

So I ask again, WHAT upper limits?

The Health Freedom Movement, as fractured and dysfunctional as it may be, is united on one idea: no unscientific restrictions on access to nutrition. At least I thought that until today’s meeting.

Since one of the people on what I would have hoped was “our team” is a lawyer, you might suspect that he would know that. And since the other is a scientist, who has made many pronouncements on nutrition and nutrient needs, including the variation of requirements for them and the very wide range of individual needs for nutrients matched to their astonishing safety profiles, you would also expect him to have had more to say than ‘we need to be aware that there is both good and not-so-good evidence and we need to be cautious on that account’. This organization proudly flaunts the fact that it is an official observer so it can speak in Codex meetings. True enough. And so perhaps we all have a right to expect that they would actually be speaking for health freedom. But what they spoke for is the dangerous status quo as defined by the Pharma Phriendly Codex folks. Why would our team (if they are our team anymore) accept and acquiesce to the notion that there should be any upper limits on nutrients? Natural Solutions Foundation is a PUBLIC observer so we cannot speak during the meeting sessions while this organization has pointed out many times that it is in the unique position of being able to speak. In fact, the lawyer for this organization stated to the Natural Solutions Foundation two years ago that he was encouraged by Dr. Grossklaus to continue speaking out since he was able to act as “the conscience of Codex”. To be a conscience, though, one has to remain true to ones precepts and beliefs, not look for acceptance and an invitation to come have a drink at the old boy’s club. What’ll you have, boys, pesticide on the rocks with a twist of genetically modified lemon?

Tribute to George Orwell: Repeat Double Speak Long Enough and It Becomes the New Truth
Another contribution that “our team” made during today’s session was to point out that the example given in one section of the Nutrient Risk Assessment document under consideration was erroneous because the negative effects of the substance referred to (Beta Carotene) were only present if the synthetic version were used but were absent with the natural version of the supplement. The example was to show how “dangerous nutrients” should be controlled. He suggested that iron would be a better example for the document’s purposes.

Shame!

While that is correct, it begs the point: whether natural or synthetic beta carotene (or any other nutrient) is under consideration, its treatment as a member of a toxic class of materials violates US law, is therefore illegal under our legislation, cannot be approved by consensus or otherwise by the US or its employees in this or similar meetings, may not be implemented in the US and represents both bad science and bad global health policy since it mandates global under nutrition in any country which becomes Codex compliant in this regard. And, as you know, the only way for a country to avoid the WTO mandates that enforce Codex is to adopt the Natural Solutions Foundation “Codex 2 Step” – while others do ‘business as usual’ your Natural Solutions Foundation proposes solutions countries (including the US!) can adopt despite Codex manipulations. Click here for a discussion of how the Codex Two Step process works. (http://www.youtube.com/watch?v=6QNg3MD6BxM) on the Natural Solutions Foundation YouTube Channel, http://www.youtube.com/profile?user=NaturalSolutions.

The Delegates of this federation also joined in the discussion of the function of the Nutrient Risk Manager which each country will have under Codex. Whom would you like to nominate for the US Nutrient Risk Manager? Perhaps this very scientist who, just a year or two ago, was actually suing the European Food Supplements Directive because they were treating nutrients like toxins and limiting their doses to absurd and insufficient upper limits. He was here today, discussing what the Nutrient Risk Manager should do, instead of demanding an end to such pernicious bureaucracy. The Nutrition Czar of each country will keep nutrients out which s/he decides are not to her/his liking and limit the doses of those which are permitted to levels favored by Risk Assessment and Risk Analysis. Does that sound like US law or the will of the US population as expressed in our law? Not to me. Is that what you want? I don’t. But “our team” participated in this meeting by rearranging the cushions on the deck chairs on the Titanic when there was an alarm to be sounded, even thought it might be less welcome to the people who called the party than their balsamic participation in the global destruction of nutritional health freedom. That’s what Dr. Ron Paul called giving FDA more authority: “changing chairs on the Titanic…” and that thought applies to Codex too… but no one there who would have “spoken truth to power” was allowed to speak. Thanks, “team”!

We stand with former Supreme Court Justice Sandra Day O’Connor who wrote for the majority in Thompson v Western States, “If the First Amendment means anything, it means that regulating speech must be a last – not first – resort… “We have previously rejected the notion that the Government has an interest in preventing the dissemination of truthful commercial information in order to prevent members of the public from making bad decisions with the information… Even if the Government did argue that it had an interest in preventing misleading advertisements, this interest could be satisfied by the far less restrictive alternative of requiring … a warning that … risks were unknown.”

On a Historical Note

Codex was, according to its own account – it’s happy picture of itself, created in 1962 and began promulgating standards and guidelines shortly thereafter. When the World Trade Organization (WTO) was created in 1994 by the Uruguay Round of GATT, the Global Agreement on Tariffs and Trade, the US law which enabled our participation in the WTO specifically prohibited “HARMonization” with any aspect which compromised our nutritional freedoms. The FDA Modernization Act of 1997 did the same and so did USC 3512. The Natural Solutions Foundation’s challenge to the FDA’s illegal determination to restrict US nutrient access to comply with Codex (which you can join here [ [http://www.healthfreedomusa.org/index.php?page_id=184]) reminds the FDA of that in strong legal terms. In 1995, despite US law, the FDA had announced in the Federal Register (October 11, 1995) that it would pursue “HARMonization” with international standards – in other words, Codex; it never withdrew this position, preferring to ignore Congress’s strong mandate. If you recall that Codex was created at the behest of the Pharmaceutical industry, that makes pretty good sense: set the situation up so that real toxins are dealt with as if they are innocuous while really innocuous – and biologically necessary- competitors to the illness industry are treated as toxins.

Then, although the idea is as absurd as needing a drug for every emotion or experience in life, or the “fact” that properly used drugs, the leading cause of death in the US, are actually good for you, the Pharma clones just keep banging away and repeating the notion that nutrients need to be strictly limited since they can be “dangerous” and eventually, if the audience is not thinking very hard or very fast, they will buy into the oft-repeated, but wrong (and dangerous) idea: “Yup! Nutrients are like dangerous toxins and should be limited as if they were. Dangerous toxins like pesticides and veterinary drugs (including antibiotics) are really OK, see, but nutrients are very, very dangerous.”

That doesn’t hide the truth: nutrients are foods!

But repeat the lie and repeat it and repeat it and, with enough propaganda and enough pseudoscience, people – governments, delegates, even the “health freedom team?” – will finally buy in to the idea as if it did, indeed, make sense. The principle is the same as repeated ads for drugs. It apparently does not make any difference that happy, healthy people running through fields of wild flowers probably do not need drugs: bring the two ideas together enough times and people will conclude that IN ORDER to be happy and healthy and run through fields of flowers gaily, they NEED drugs. So … ask your doctor! And ignore the rapid fire, quickly intoned and quickly forgotten reality disclosures of what these drugs do to you, whether you need them or not.
Back here in Codex-land, the Sunday morning session was a short one, just two hours, to discuss Risk Assessment as it applies to nutrients was a short one, just two hours. And it ended about 45 minutes early. The work was done rapidly and with seeming banal boredom. No passion, all civility. Quietly and politely set up a system that will condemn who knows how many people – billions? – to chronic under nutrition and what the World Health Organization identifies as its inevitable results: cancers, cardio-vascular diseases, stroke, diabetes and obesity. Here in Codex-land we can just decide to treat nutrients as if they were dangerous toxins. That lets us set minimum intake levels (since, unlike toxins, even in Codex-land a total lack of nutrients is a very bad thing). In fact, the Australian Chairwoman of the meeting noted that traditional Risk Assessment does not apply to things which are necessary for life, only to those which are toxic to us. “Modifications” which have never been tested by science, have been made to the Risk Assessment profile and procedure to account for this difficulty. Never mind that these modifications have no scientific validity. The much-vaunted “Science Based” ethic of Codex is, as it says in Porgy and Bess, “a sometime thing”.)
Once the inhabitants of Codex-land got that point established, they could make the decision to set nutrient upper limits (ULs) since, here in Codex-land we don’t want people to have enough nutrients to stay, or get, healthy. Remember, not only did Dr. Grossklaus, the Chairman of CCNFSDU, state in 2003 that “Nutrition has no role in health” but even if it did, it would not be permitted. You see, “healthy” is a very, very bad idea here in Codex land. Sick and taking drugs in Codex-land. Now THAT’s a good idea!

The Council for Responsible Nutrition,, or CRN, a US supplement trade group, has been a huge fan of setting upper limits for nutrients using Risk Assessment. (see, for example, http://www.crnusa.org/pdfs/CRNCommentsCAC062804.pdf )

I was not really looking, after all this time, for much support for the idea of high potency nutrients as our legal right in the US from Council for Responsible Nutrition, whose John Hathcock was at the meeting asking for limits to guide manufacturers, no matter how low, nor from the IADSA, http://www.iadsa.org/ , the, International Alliance of Dietary Supplement Associations, another trade group which seems to have missed the point that if nutrients are limited to doses so low that they, by design, have no impact on people, then people will stop buying nutrients. Duh! In other words, the supplement industry is blindly shooting itself in the pill bottle. Could that be because of the guidance it is getting from its trade organizations, NPA ( http://www.naturalproductsassoc.org/site/PageServer ) and CRN? And could THAT be due to the influence of their board members who are from drug, biotech and Agribiz industries, whose wishes and whims control Codex? Hmmm.

I was not looking for their support in protecting your high potency self determination from CRN or IADSA and I was not disappointed. It is true, I must admit, that John Hathcock did kindly point out that the Codex Two Step” (a template which we have applied to the Codex Vitamin and Mineral Guideline in our Codex eBook ( http://www.healthfreedomusa.org/index.php?page_id=220), is a valid process and open to any nation that wants to use it. He did not call it that, he just identified the portions of the WTO trade agreements which makes it both legal and accessible to any country which wishes to protect itself from Codex. So thank you for that, John. It is also true that the attorney representing the “Health Freedom” federation at this meeting has repeatedly condemned, derided and scoffed at the Codex Two Step process. As a lawyer, I would have expected better. So Mr. Hathcock got that point, at least, exactly right.

But the two “Health Freedom” team members? Where were they? Rearranging the cushions.

Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org

*Dietary Supplements Health and Education Act, passed in 1994 by unanimous Congressional Consent says that nutrients are foods which are generally regarded as safe.

Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org

*Dietary Supplements Health and Education Act, passed in 1994 by unanimous Congressional Consent says that nutrients are foods which are generally regarded as safe.