Archive for the ‘Activism’ Category

Dr. Rima Reports: Congress Does Not Want to Hear from You!

Tuesday, March 1st, 2011

Natural Solutions Foundation
Your Voice of Global Health & Food Freedom™
www.GlobalHealthFreedom.org
www.GlobalFoodFreedom.org

Newest Anti Freedom weapon from the US Congress: You’ve Got a “Poor Reputation”!

Electronic warfare is not just death rays and microwave crowd control anymore. Certain members of the US Congress have decided that when you tell them what you want – and it is not what their corporate masters want – YOU have a bad reputation. That’s why some of you have been experiencing “email returns” when you attempt to send messages through our Action eAlert Educate Decision Makers system. We have some solutions to implement. Read on.

Take Action!

Take Action!

Got a bad rep? We certainly hope so!
Good reps need not apply!

Democracyinaction.org (DiA) is home to many small organizations like ours (and some really big ones, we understand). The Foundation pays for a suite of electronic tools from DiA’s Salsa system to allow us to keep in touch with you and you to communicate, efficiently and effectively, with decision-makers, including, but not limited to, the US Congress, the White House, the Secretaries of Cabinet Level Departments, FDA, State legislators, governors, etc.

You click a button and people get your emails telling them what we do – or do not- accept, want, desire, demand. You can use our current Seven Action Items for Health and Food Freedom here: http://www.healthfreedomusa.org/?p=8653 and can read about your successes here: http://www.healthfreedomusa.org/?p=195 — PUSH BACK works!

But now, in its latest round of anti-Constitutional, anti-freedom assaults on you and me, elements in the US Government has decided that this organization, which allows people to communicate with the people who impact their lives, sometimes in a lethal way, has, and I quote, a “POOR REPUTATION”!

Never mind that the approval ratings of the people we correspond with, with very, very few exceptions, among people who are even semi-conscious, show that they have a dismal reputation. [Congress has about a 25% approval rating http://www.pollingreport.com/CongJob.htm]

Never mind that this dismal reputation has been earned for Congress and elected “leaders” by their raping our rights, pilliging our protections, destroying our democracy, eviscerating our environment, macerating our monetary system and stealing us blue, blind and Sunday.

Never mind that these criminals are puppets in the hands of absolutely dastardly forces and, with their own health care system securely in place, have given us over to the worst of the worst allopathic atrocities for OUR illness management.

Never mind that they have agreed to give Monsanto and their ilk control of every bite of food in the US food chain and never mind that they have turned a blind eye to reality, the Constitution and the future of the country and the planet.

WE have a Bad Reputation? Democracy in Action has a Bad Reputation?

I, for one, am proud to be a card-carrying BRP — “bad reputation person”!

Yes, I say. My reputation for willingly being enslaved proceeds me. It is bad.

My reputation for sitting silently while deadly, unnecessary vaccines are foisted on me and my children and their children is really, really bad.

My reputation for bowing my head and bending my knee to my supposed “betters” who want to steal the wealth of my country and my world for themselves while we, the “Useless Eaters” of the world are picked off, millions at a time is terrible.

My reputation for accepting the lies which corporate media and corporate government and government corporations and corporate person hand out to me is truly unrepentant and shamelessly awful.

My reputation for agreeing to be dumb and down is definitely dismal.

How is your reputation? If it is as bad as mine, then welcome to MY WORLD!! It is a world in which bad slaves and servants stand up to their would-be masters and take back their freedoms. It is a world in which the chaos and lies get sorted out through ringing the bell of truth because it resonates in the hearts and minds of men and women of character (and bad, bad reputation) everywhere. One step we’re taking, to take back our sovereignty: we’re adding the words “US Citizen” to the subject lines of the Action Items. Some of our Mouse Warriors have reported to us this seems to have an impact. Just some more PUSH BACK!

And — our would is the world of effective activism.

If you are an inhabitant of my world, then you are an activist. You take the Action items, you disseminate them, you call Congress when Congress says talking to them gives you a “bad reputation” and you say that you are the employer of the Congress Members of your State and District and that you WILL be heard.

And, yes, you donate to the Natural Solutions Foundation.

In some other world, there is no need to shoulder any financial burden to get what you want, or pay for what you desire. Please reserve me a seat on the first transport there. But the reality is, at least in this world, that there are real expenses to running an organization and making change happen.

It’s your world as well as mine, after all. We are in this world together.
We are in this stuggle [for our lives] together. Donate here.
http://www.healthfreedomusa.org/?p=189.

And thank you!

Yours in health and food freedom,
Dr. Rima
Rima E. Laibow MD
Medical Director
Natural Solutions Foundation
www.DrRima.net
www.NaturalSolutionsFoundation.org
www.MyValleyoftheMoon.org
www.ValleyoftheMoonCoffee.org
www.FoodFreedomeJournal.org

Natural Solution’s Chiriqui Times Online

Sunday, February 13th, 2011

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Permalink: http://www.healthfreedomusa.org/?p=8391

FDA Seeking to Outlaw IV Vitamin C, Other Nutrients

Friday, January 7th, 2011

FDA Seeking to Outlaw IV Vitamin C, Other Nutrients
Rep. Ron Paul, MD: As an agency, FDA engages in “abuse of power…”

“FDA: Leave Our Nutrients and Supplements Alone!”
Action item: http://tinyurl.com/saveIVNutrients

Archive of Emergency Web Meeting of January 9, 2011 here:
https://naturalsolutionsfoundation.webex.com/naturalsolutionsfoundation/ldr.php?AT=pb&SP=MC&rID=2625702&rKey=9f5c8c59f61ba89a

March 9, 2011 – We Dissect a Response from the FDA! Click Here.


The FDA (the Food Destruction Agency) not content with its new power to control and industrialize our entire food supply, is, quite predictably, increasing its attacks on nutrients. Although the mis-named Food Safety [sic!] Modernization Act excludes nutrients, the FDA’s rampage against natural health is by no means limited to degrading our food supply.

DSHEA, the 1994 Dietary Supplements Health and Education Act, which protects dietary supplements does not protect nutrients unless they are delivered in oral form. That means that intravenous, transdermal, nasal, suppository or other forms of nutrition are vulnerable to FDA assault in a particularly worrisome way. This latest action by the FDA makes that point clearly.

On December 28, 2010 FDA ordered certain small manufacturers to stop making IV Vitamin C and several other injectable nutrients which are always used under a (holistic or Advanced health Care) physician’s supervision by classifying IV Vitamin C, Magnesium and certain B Vitamins as “New Drugs”.

The nutrients under attack, which form the basis of the popular “Myers Cocktail” and countless therapies for serious diseases, may be provided ONLY by compounding pharmacies under a specific prescription for a specific patient. This means that the cost of these nutrients will increase sharply.

It also means that the FDA, always hostile to compounding pharmacies and the independent use of nutrients, bio-identical hormones (now banned at the request of Wyeth/Pfizer, which manufactures dangerous synthetic hormones), the biologically active form of Vitamin B-6 (also banned at the request of a drug company) can pick off individual substances and attack compounding pharmacies at their leisure. This is a result of the power granted FDA in 2007 (section 301(11) of the Kennedy FDA Enabling Act) to ban interstate sale of any “food” ever studied for medical use, even if never so used.

Why, you ask, does FDA need authority to ban safe foods? Why does Congress think it has the power to grant such authority? Where in the Constitution does Congress have that power? And please, don’t say it’s in the “Commerce Clause” which grants the Federal Government the power to regulate Interstate Commerce. “Regulate” does not mean the power to forbid foods that people have always had the fundamental human right to grow, trade and use. It merely means to make commerce regular; to make fair and neutral “rules of the road” for Interstate Commerce. Under the 9th Amendment, the People have retained the right to grow and trade foods, including vitamins and minerals. As we Restore the Republic, that right must be respected again.

Manufacturing companies wishing to make and sell the now restricted injectible, inexpensive and life-saving nutrients will be forced to engage in full-scale drug approval testing for products that cannot be patented; this, the FDA knows, is economically impossible. The attack on Vitamin C comes on the heels of efforts by FDA to ban other nutrients, including forms of Vitamin B6 banned under the Kennedy Enabling Act.

If these restrictions stand, what nutrient will be next?

Please take the Action Item at this link, which tells the White House and FDA to leave our nutrients alone! http://tinyurl.com/saveIVNutrients

Blog entry originally published at: http://vitaminlawyerhealthfreedom.blogspot.com/2011/01/fda-seeking-to-outlaw-iv-vitamin-c.html


ONE OF OUR SUPPORTERS GOT A REPLY FROM THE FDA
ABOUT IV NUTRIENTS; WE DISSECT IT…

— On Wed, 3/9/11, CDER DRUG INFO wrote:

From: CDER DRUG INFO
Subject: RE: Leave our Nutrients Alone!
To: “‘[redacted]'” Date: Wednesday, March 9, 2011, 8:53 AM

Dear P… B…

Thank you for your e-mail expressing concerns about FDA’s December 28, 2010 warning letter to an individual manufacturer (McGuff Pharmaceuticals Inc.) of intravenous (IV) vitamin C along with other prescription drugs.

Unlike oral vitamin C-which could be a dietary supplement- these particular IV solutions are, by law, unapproved drugs. Moreover, the manufacturers neglected to follow current good manufacturing practices, potentially exposing users to unnecessary risks.

Such risks have occurred before. In the E-Ferol tragedy of 1983, premature babies received E-Ferol, an intravenous form of vitamin E. E-Ferol was associated with adverse reactions in 100 premature infants, forty of whom died. It is highly likely that this tragedy would have been prevented if the product had been reviewed and approved by the FDA before its introduction to the market.

Since FDA announced its Unapproved Drugs Initiative in June 2006, marketers of unapproved drugs have been on notice that addressing risks from unapproved drugs is a high priority for FDA, and that the Agency plans to systematically and responsibly ensure that all products on the U.S. prescription drug market become compliant with current FDA approval requirements for safety and efficacy.

The mission of FDA’s Center for Drug Evaluation and Research (CDER) is to ensure that safe and effective drugs are available to the American public. Drugs that have not been approved by FDA may not be safe and effective, may have been manufactured under sub-standard conditions, may contain too much or too little (if any) active ingredients, and may not have necessary labeling information and warnings.

FDA’s drug approval process ensures that drugs are safe, effective, of a suitable quality and purity, and are properly labeled. The Agency remains committed to assisting all firms with meeting these standards.

Again, we thank you for your input and hope that we were able to address your concerns.

Best regards,

Division of Drug Information – JD
Center for Drug Evaluation and Research
Food and Drug Administration

For up-to-date drug information, follow the FDA’s Division of Drug Information on Twitter at FDA_Drug_Info

This communication is consistent with 21CFR10.85(k) and constitutes an informal communication that represents our best judgment at this time but does not constitute an advisory opinion, does not necessarily represent the formal position of the FDA, and does not bind or otherwise obligate or commit the agency to the views expressed.

Please note: the above statement, in our humble opinion, misstates the law. The various laws passed by Congress over the decades continually adding to the FDA’s power all include “grandfather” clauses allowing products that existed when the various laws were adopted — IV nutrition has been used for a very long time. Andrew St Georgie received the Nobel Prize as one of the discoverers of Vitamin C in 1937. Frederick Klenner, M.D used IV Vitamin C in the 1940s. It was used IV well before the 1952 authorization by Congress giving FDA authority over the “safety and efficacy” of drugs (before that time, FDA only had authority over misbranded or adulterated drugs). rf

“From 1943 through 1947,” writes Robert Landwehr (3), “Dr. Klenner reported successful treatment of 41 more cases of viral pneumonia using massive doses of vitamin C. From these cases he learned what dosage and route of administration – intravenously, intramuscularly, or orally – was best for each patient. Dr. Klenner gave these details in a February 1948 paper published in the Journal of Southern Medicine and Surgery entitled ‘Virus Pneumonia and Its Treatment with Vitamin C.’ (4) This article was the first of Dr. Klenner’s twenty-eight (through 1974) scientific publications.”

It might be interesting to learn how poliomyelitis was treated in Reidsville, N.C., during the 1948 epidemic. In the past seven years, virus infections have been treated and cured in a period of seventy-two hours by the employment of massive frequent injections of ascorbic acid, or vitamin C. I believe that if vitamin C in these massive doses – 6,000 to 20,000 mg in a twenty-four hour period – is given to these patients with poliomyelitis none will be paralyzed and there will be no further maiming or epidemics of poliomyelitis.’ Levy concludes: “The four doctors who commented after Klenner did not have anything to say about his assertions.”

Klenner administered ascorbate by injection, and, as Lendon H. Smith describes in great detail in the Clinical Guide to the Use of Vitamin C: The Clinical Experiences of Frederick R. Klenner, M.D., Klenner found that “the most effective route was intravenous, but the intramuscular route was satisfactory. He gave at least 350 mg per kilogram of body weight.” That quantity per day is a dose of 25,000-30,000 mg or so for an adult. Yet, Smith adds, “With 350 mg per kilogram of body weight every two hours, he could stop measles and dry up chicken pox.”

http://www.doctoryourself.com/klennerbio.html

Defending the FDA: Being the Devil’s Advocate

Thursday, January 6th, 2011

Natural Solutions Foundation
www.GlobalHealthFreedom.org

DEFENDING THE FDA

Our Indictment of the FDA for Crimes Against Humanity is at: http://www.healthfreedomusa.org/?p=8073.

This note is from one of our Health Freedom Warriors: “In case you are having trouble getting lawyers to volunteer to defend the FDA, it’s not that hard, really, for a well-trained lawyer to set aside his or her feelings, thoughts and humanity to just express the client’s inner truth. Sort of like channeling… Their case is practically ready-made, they’d just need to fill in the details. Basically it boils down to the following, which came to me in a dream… where I thought I saw a 40-foot stone owl in some dark Grove somewhere, acting as the FDA’s counsel and intoning…”

Members of the Jury of our Peers,

1) You can understand that my client (the FDA) needed the money, and the only really good source of money happened to be the drug dealers. These drug dealers are not some kind of illegal street dealers selling deadly drugs on the street. Certainly not! We despise such people! No, they are highly respected pillars of business and civilization, selling deadly drugs in the medical system, where they are all legal, and recognized as advanced science. Fair warnings were given to the doctors and patients that these drugs would kill those who took them; it was never a secret to those who knew where to look for the information. My clients are, after all, legitimate businessmen and none of their fathers were charged at Nuremberg… well, hardly any of them.

2) Defendant Agency understands that the Earth today is way too crowded for the comfort of folks like us. Just ask any impartial source, such as, say, the Georgia Guide Stones, or any of the academics ensconced in their corporate-sponsored University Chairs. When you understand that even all our efforts during WWII and the Cold War, killing only about two hundred millions, barely slowed population growth (they just don’t die as young as they used to) you’ll understand that my client is actually performing an extraordinary public service by helping mother Earth escape from this crushing burden.

3) Doctors today are extremely tired (could it be their chronically poor nutrition — no, not possible, since we know scientifically that nutrition has nothing to do with health and well-being). So these duly licensed illness-care processors must be relieved of having to think so much. My client makes sure that doctors get to rest more, as under Obamacare we can now make all of their decisions for them. We run the national illness payment system. We give the docs the drugs they can use to stop every patient complaint. And if those symptoms get replaced with a more serious, more lucrative problem, well, aren’t you glad we’re there to help? Why study physiology and diagnosis when you can just read our suggested list of products and how to use them? You know, one product to suppress the symptoms of, say, heart disease brought about by a life of poor nutrition and little exercise, then another drug to cover-up the side-effects of the first drug, and on, and on, to our mutual profit. Ah! I get little tingles up my spine whenever I contemplate it… or are those mini strokes We have a drug for that too!

4) A few physicians don’t “get it” and insist on old-fashioned preventative medicine, avoiding toxic overload (as from vaccines and our other wonderful drugs) and eating wholesome food. The medical authorities usually take care of those malcontents. We make it easy for illness-care personnel. Now anyone can figure out which of those two paths is easier: work with us, or else… And if doctors are more rested, and less stressed by having to think all the time, they will feel better and prescribe even more drugs, which we know have been scientifically proven to not kill more than 150,000 American a year when properly prescribed in a hospital setting. Thus we are helping to raise the level of medical care one doctor at a time (well, actually one million doctors at a time, but you get the idea).

5) We have saved the nation millions of dollars by making it unnecessary to write the curriculum for medical schools. We offer this service in the spirit of humanitarianism, and we do it for free, showing young doctors how our drugs suppress any symptoms a patient may exhibit, so the doc doesn’t have to worry. Instead, the doc can prescribe more drugs to deal with side effects. You know, all drugs have effects on the body, distorting normal function, and those effects we are marketing are the “therapeutic effects” and those that we’d like to ignore are the “side effects” — you do see the logic in that, members of the Jury, don’t you?

6) We are helping young people to understand health at a far earlier age, by seeing drug ads every day on TV. In fact with improved access to drugs available for children of younger and younger ages, we are letting them actually experience the great enjoyment of being able to get rid of the confusion of growing-up without having to understand the cause. This can be the foundation of the wise life philosophy known as avoidance, which has saved millions of people countless hours of agonizing thinking and analysis, and replaced it with instant removal of any discomfort with pharmaceuticals and the deep satisfaction of unconsciousness. We do not endorse the use of illegal street drugs and deny that the culture of drug-taking, advertising for which we spend billions annually, has anything to do with the pandemic of drug use… and aren’t you relieved that there is no autism epidemic caused by vaccines and other toxins? The FDA has made that scientific finding which none may question. But don’t worry; we have plenty of drugs to keep those distracting autistic and otherwise neurologically damaged kids quiet!

7) My client has demonstrated an unswerving devotion to the greatest good for the greatest number of shareholders, by helping to eliminate those who will not be among that greatest number, in a way that is most humane to them, in spite of the fact that they are lower level life forms, compared to us, the initiated elite. If that is not compassion, let me know what is.

8) In short, my client, the FDA, should not only be acquitted of all charges, but should be recognized as the first ever US Agency recipient of the Nobel Prize for peace through euthanasia (albeit gradual in most cases). The agency is a glowing example of our Globalist Eugenicidal Agenda. This is obviously the most direct path to world peace.

And finally, my client reminds you to look for the wise bumper sticker (you may have seen it) that summarizes the most direct solution to our ecological problems. It says “Save the Planet. Kill yourself.” It was created specifically for members of the lower classes of humans (i.e. the 90% of whom we know are “useless eaters”). Such deep meaning, such eloquence! [Ah! Reminds me of when I was initiated into the Order… but that’s another matter.]

And, in case you, the little people, don’t have the guts to act on what that bumper sticker suggests, we, the elite, understand, and we’ll help you, through the actions of my client and its esteemed associated agencies and corporations, get it done.

Now if that’s not public service, there is no such thing. The Defense rests.”


Dr. Rima on the Globalist Eugenicidal Agenda

J’Accuse – We Accuse the FDA of Crimes Against Humanity

Wednesday, January 5th, 2011

WE ACCUSE THE FDA!
The Citizens Commission for Health & Food Freedom
J’Accuse … Indictment of the FDA

Dr. Ron Paul: the FDA engages in “abuse of power…”

This Citizens’ Indictment is Presented to the Court of Public Opinion
Permalink: http://www.healthfreedomusa.org/?p=8073
Action Item: Demand Redress of Grievances! Tell Congress to Protect our Rights!
http://tinyurl.com/4r5rr6w

You of the United States Food and Drug Administration (FDA) leadership are little more than political hacks, which means that you are little more than prostitutes for the Multi-National Corporate Persons who would poison you and your children while they poison us and ours.

You have blood on your hands, FDA officers and agents, blood mixed with chemicals. Your scientists tell you that mercury amalgams have no place in children and you choose to ignore their pleas telling you that patients need protection; instead you aid and abet mass poisoning of children and adults with toxic mercury and with toxic fluoride; you merely offer to cover-up the harm by having people sign more abusive waivers to protect the dental and corporate interests who poison their brains and bodies.

Your experts told you that “GMO” genetic modification of plants and animals was tinkering with life itself and, once released, this particularly malignant genie could never be re-contained in its flask. “Do not do this!” they said, but you rushed not to judgment, but to the condemnation of our biosphere, one nuclear DNA bundle of precious genes at a time, throwing out bouquets of infertility, cancer, brand new lethal allergies, strangely mutated bacteria, weeds that will not die, babies that cannot live and a plague of contagious genes never before seen – or experienced – on this planet. You have conspired to allow the poisoning of the biosphere.

Your bloody hands, hearts and heads have no capacity to contain all the guilt for deaths and suffering, losses and heartbreak caused by poorly tested (or in the case of flu vaccines, not safety tested at all), deceptively reported and dishonestly labeled drugs and vaccines which you had every reason to know will kill and main, but from which you make money or receive research position and money. Such a small amount of money, FDA, for so many lives despoiled and destroyed.

You are baby-killers. We accuse you of purchasing, approving, recommending, allowing, distributing and promoting the 2009 H1N1 Swine Flu Vaccine which has resulted in thousands of miscarriages. See our Citizens Petition demanding that you enforce the law against vaccine drug pushers: http://www.healthfreedomusa.org/?p=7418

Your dishonest and self-serving regulations make food the stuff of death and drugs the stuff of suffering. The fluoride in the water which you criminally flood us with – for genocide and mind control is a crime against humanity – is not there for us and our well being. It is there for the profit of those who would poison us and the comfort of those who would dominate us through apathy and slack-witted mindlessness.

FDA, you know that we know how to control disease and remove its underlying causes and you know that such removal and control strikes deeply at the heart of the Uber Cartel, those drug lords who will sell their contaminating agra-chemicals and provide their death-dealing seeds in order to make short term money, gain long-term control and accomplish forever-term depopulation of those of us deemed unnecessary, the “Useless Eaters”.

So J’Accuse FDA. We accuse you of murder, of graft, of extermination, of inhuman acts committed against the civilian population of the Earth, the military population of the Nation, unborn generations of the planet. I accuse you of Crimes Against Humanity through knowingly perpetrating these acts. I accuse you of fast-tracking death because it brings fast-track profits and because it brings fast-track infertility, suffering, disease and death.

We accuse you of having neither shame, compassion nor any humanity worthy of the name. You have sold your soul, FDA leadership, for a mess of guilt, crime and money.

For the brothers, sisters, mothers, fathers, sons, daughters and others of the Earth, We accuse you of genocide.

The International Criminal Court statute (echoing the Nuremberg Code) provides, in Article 7 of the Rome Treaty that Crimes Against Humanity, even when practiced against one’s own people, include “Other inhumane acts … intentionally causing great suffering, or serious injury to body or to mental or physical health.”

We therefore accuse the FDA and its officers and agents of conspiracy to cause “serious injury to body or to mental or physical health…”

FDA: how do you plead?

The Trustees will announce the membership of the Citizens’ Commission over the next few weeks and will then develop the case against the FDA for presentation to the Commission and their Moral Decision. We need a lawyer to volunteer to defend the FDA. Any volunteers?

[Update: Defending the FDA – Being the Devil’s Advocate: http://www.healthfreedomusa.org/?p=8078.]

Maj Gen Bert Stubblebine (US Army ret), President
Rima E. Laibow MD, Medical Director
Ralph Fucetola JD, Counsel
Natural Solutions Foundation Trustees

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