Archive for GMO – Page 3
Natural Solutions Foundation
The Voice of Global Health Freedom(TM)
www.HealthFreedomUSA.org www.GlobalHealthFreedom.org
Permalink: https://staging.drrimatruthreports.com/?p=6292
Lynn McTaggert publishes the interesting UK-based “What Doctors Don’t Tell You” newsletter and materials. We have never met but I read her material and hope that she reads ours.
Recently I read a heartfelt plea by Ms. McTaggert crying out for someone, anyone, to understand that health freedom and the restrictions of nutrients and natural health options (to which, of course, I would add both food and the right to refuse or use any treatment you wish), when under attack, IS their problem.
In 2002, when Ms. McTaggert saw what was going to happen to natural health options in the EU, she convened a meeting to which few came and fewer paid close and productive attention.
Her experience was so like mine that I felt compelled to answer her experience in the UK with ours here in the US. Please read her article after you read my response and you will see why YOU are the lynch pin. It is you, after all, who can mobilize your contacts and help them to get active and involved.
It is you who will take the Action items that keep the globalists off balance and backing up. And it is you who shoulder the responsibility to whatever degree you can, to keep the health freedom battle alive and kicking. Click here, now, to make your recurring donation to the Natural Solutions Foundation. It is, you see, your problem.
And thank you!
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Natural Solutions Foundation’s Valley of the Moon(TM) Eco Demonstration Project
www.NaturalSolutionsFoundation.org
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www.ValleyoftheMoonCoffee.org
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My response to Lynn McTaggert’s WDDK article “Not My Problem”,
I am the Medical Director of the Natural Solutions Foundation, www.HealthFreedomUSA.org and www.GlobalHealthFreedom.org.
I have practiced natural, that means drug free, psychiatry and medicine since I was graduated from the Albert Einstein College of Medicine in 1970.
It was clear to me for a couple of decades that these assaults on our health freedom, and the right to access clean food, natural health strategies and pharmaceutical alternatives was under an increasing crescendo of attack.
It was clear to me by 2004 that our side was doing nothing much productive to counter effectively what the Uber Cartel, led by Big Pharma, were up to: globalized health and freedom suppression and genocide through illness based on dangerous drugs, pollution and devitalized foods that do not sustain health, let alone life.
Realizing that there was no road back once these changes were institutionalized, my husband, Maj. General Albert N. Stubblebine III (US Army, Ret.) closed our practice of drug free medicine, sold our house and created the Natural Solutions Foundation.
Why didn’t we just join forces with other health freedom organizations? Well, we tried. The first thing we did was call a well known health freedom advocate and offer our help and support. financial and otherwise. His response? “I do not like you because I do not know you, I do not trust psychiatrists and there is nothing you can do for health freedom. Just send money and leave me alone.” That is a direct quote.
We were so appalled that an apparent leader of this “movement” would be so short sighted and self absorbed, with no better prospects on the horizon, that we were catapulted into our decision to take this battle on since no one particularly effective or strategy-minded was on the scene.
Next, we met with other people in the “movement” and suggested in early January, 2005, a meeting of all the groups involved in this battle, much as Lynn did. That meeting took 6 weeks to organize. Most of the invitees did not come. Those who did were most occupied with slashing at each other behind backs and to faces. The outcome was predictable: nothing of any use whatsoever.
We were told that people were cowed by the vicious attacks of the first person I mentioned and so, in true co-dependent fashion, allowed the least stable person in the system make the most important decisions through bullying.
Another so called “leader” called us up and told us that we were not “permitted” to run a health freedom rally because “Health Freedom BELONGS [emphasis added] to the XXXX Foundation, as does all money involved in health freedom.” Again, not a very productive approach to winning a war, one might say.
And so it went. Petty jealousy, foolish self-interest and a movement so out of control that it could only be explained by ego or agents provocateur, or, as we believe the case to be, both.
Another example: in the US, where the Natural Solutions Foundation is based, we had a unique phenomenon develop during the most recent Presidential elections: through www.Change.org we were able to create the 10 top issues in the US according to people’s electronic votes. Those issues would, we learned, be presented to the newly elected President of the United States as the major concerns of the people of the US.
We seized the opportunity and created a health freedom item. We then wrote to every health freedom organization asking them to join with us to bring our issue to the forefront of awareness. The name of our organization did not appear anywhere in the item. We asked all of these organizations to urge their members to use their collective power and move the Health Freedom item up to number 1.
What did they do? Several of them actually banded together to urge their members to use the voting format to vote DOWN the health freedom item because they were not the initiating organization.
We made it, if I recall, to Number 8, if I recall, which was enough to be included in the top 10, but hardly where the issue should have been.
And, of course, every time the Natural Solutions Foundation accomplishes something like, for example, forcing the disastrous phony Food Safety Bill off the voting agenda, or stops the mandatory Swine Flu vaccine program the federal government was planning in the US, we get attacked as – of all things – “controlled opposition”.
Then there are the manufacturers and business people. Exactly as Lynn described it, when their ox is being gored, they have a hard time seeing it. When their ox is not being gored, they could not be less interested, many of them. Of course, there are the far sighted exceptions, but I share with Lynn the awareness of how important action is and how little the organizations and, in many cases, the companies involved are willing to see beyond their own noses.
So, in essence, it is up to us, the people.
The Health Freedom Organizations are either infiltrated, underfunded or ineffective. The Wellness companies are either blind or so burdened trying to stay in business that they cannot see the forest for the trees even though the forest is advancing like the forest in Macbeth!
What to do? Exert the strength of a powerful netroots and take this struggle on as your own. Because it is. What we are struggling about is not pills and powders. It is health and freedom, the right to control our own bodies, make our own choices.
It is the right to seek, or refuse, any treatment or health strategy which we desire.
It is the right to access clean, unadulterated food and high potency nutrients because we want to, under whatever terms we want to use them.
It is the right to share and study truthful information about the benefits of food and food components in a climate of free inquiry, not criminalization or regulatory gag rules, as is currently happening under Codex and in the US.
Just weeks ago, the European Parliament agreed to stop requiring the labeling of GMO “foods” and ingredients. This is a horrific blow to your freedom in Europe, which has already been accomplished in the US where such labeling is FORBIDDEN. This, of course, follows the secret meeting of the 27 heads of state of Europe last October 22 in London to find ways to compel the people of the EU to accept GMO foods despite their vigorous objections to it.
Gag rules to prevent health information (called “claims”) from being shared are the order of the day of the corrupt and industry-owned FDA (which we in the Natural Solutions Foundation refer to as the Fraud and Death Administration) and are one of the tools of Codex to make sure that your only options are drugs and, eventually, death, after serious profit from that death march.
Truly, either we do what needs to be done, or what they want done to us will prevail.
I urge you, wherever you live, and whatever you eat, to become part of the thrust for freedom. Health and Freedom are essential components of one another. Health Freedom IS Our First Freedom. Please join the free, secure Health Freedom Action eAlerts here, www.GlobalHealthFreedom.org, or here, www.HealthFreedomUSA.org, and join us in securing our Health Freedom once and for all.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
Comment available at:
http://www.theintentionexperiment.com/not-my-problem.htm/comment-page-1#comment-7081
And here is Lynn’s poignant article:
Not My Problem
August 6th, 2010
In 2002 my magazine What Doctors Don’t Tell You first learned about plans within the European Union to radically restrict natural medicine across all member countries, starting with laws that would create a very low ceiling of ‘safe upper limits’ in vitamins.
Although the laws were ostensibly to create a level playing field within the European supplement market, the proposals bore the heavy hand of Big Pharma.
At the time, the solution appeared simple. The majority of people in the UK use some form of natural medicine. All we needed to do was to band together, whip up a national protest, and the laws would be stopped in their tracks.
In early 2003, we invited all the heads of the largest vitamin companies and representatives from all the leading natural medicine organizations – homeopathy, herbal medicine, traditional Chinese medicine, acupuncture and many others – to a meeting in central London.
Many of the organizations never showed up. Of the 50 or so who did, many groups felt that our concerns were alarmist. Others welcomed the new moves as good for business. A few attempting to fight the legislation were busiest fighting each other.
No group seemed able to see the bigger picture. Each organization was mainly concerned with whether their own business was under fire. If it wasn’t – and at the time it wasn’t for many of the disciplines – they weren’t interested. Not my problem.
Big Pharma had big plans all those years ago. Unless there is sufficient opposition, within the next year or two, laws will come into effect in Europe that will drastically restrict the access of all Europeans to high-dose vitamins and herbal medicine.
Most therapeutic herbal medicine, plus forms that are new to the West, such as Ayurveda and Traditional Chinese herbal medicine, will effectively be banned. And although homeopathy has emerged unscathed from future EU law, the British Medical Association is working to eliminate funding for NHS homeopathic hospitals.
This pogrom will not end in Europe. The near identical international laws that have been drafted within the United Nations suggest that a well organized and concerted effort is under foot to finish off any alternative to orthodox medicine.
The plan is to watch Europe closely to assess the level of consumer protest. Thus far, that protest has been minimal. The two consumer groups that have maintained any sort of consistent attack – the Alliance for Natural Health (ANH) and Consumers for Health Choice who have challenged the law and lobbied parliament are starved of funds.
The individual organizations to this day remain isolationist. Not my problem.
This attitude reminds me a bit of the speech given by Pasto[r] Martin Niemoller about the passivity of many German groups to the purging by the Nazis of group after group.
First they came for the Jews,
and I didn’t speak up because I wasn’t a Jew.
Then they came for the communists,
and I didn’t speak up because I wasn’t a communist.
Then they came for the trade unionists
and I didn’t speak up because I wasn’t a trade unionist.
Then they came for me for me
and then there was no one left to speak out for me.
For all of us wishing to maintain alternatives to drug-based orthodox medicine, these laws are all of our problem, and every last one of us has an obligation to speak up now…..
Natural Solutions Foundation
The Global Voice of Health Freedom(TM)
www.HealthFreedomUSA.org www.GlobalHealthFreedom.org
Permalink: https://staging.drrimatruthreports.com/?p=6276
JOIN THE PUSH BACK! BAN GMOs NOW! Click here now: http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=2049 and forward this link to all of your contacts to make sure that we end the GMO menace NOW!
PUSH BACK! THEY TELL US IT CAN’T BE DONE. THEY ARE WRONG!
Save Food and Keep It Safe NOW! Take Action here to protect food from the dangerous fake “Food Safety Bill”, S. 510 which could be passed in the Special Session of Congress or in September. This is an urgent danger and we need your help. This is a new Action Item so even if you have registered your opposition to this bill before, please do so now by clicking here: https://staging.drrimatruthreports.com/?p=6269. Now send this to all of your contacts asking them to take action and send it along for similar push back.
For your clean food pleasure, give yourself a present with Valley of the Moon(TM) Coffee grown as a teaching project of the Natural Solutions Foundation to help reclaim the production of food. Click here, http://www.ValleyoftheMoonCoffee.org, to support your health freedom and your body at the same time. We suggest our 100% GMO free, toxin free Health Freedom Coffee for your Holiday Gifts, including all your Corporate Gifts! Contact us at nsfmarketplace@gmail.com for more information on multiple bag purchases.
PUSH BACK! LET’S HEAR IT FOR PUSH BACK! AND THEN, LET’S HAVE A WHOLE LOT MORE OF SAME.
Using the Courts, the Court of Public Opinion, Political Pressure, Radio and TV, Video Action Items in the Health Freedom Action eAlerts and similar publications, We, The People, are, in fact, exerting our power. We do not win every battle, but we win and win and win when we push together. This time, the victory is the reversal of a clearance for a dangerous GMO to be grown without restraint or supervision.
Children are among the major consumers of sugar. Sugar beets are among the major sources of sugar. Genetically modified sugar beets are adapted to survive the use of deadly chemicals. That is, in fact, despite the propaganda and hype, the only reason that most GMOs are created: to create an after market for deadly chemicals. Of course, the sales of GMO seed help the bottom line along for the Uber Cartel but the real money is in the increased use of, and subsequent sale of, the profitable chemicals which the same companies make. Oh, yes, of course they are also drug companies so they get you coming into the food cycle and the hospital when they sell you drugs for the conditions and diseases which their chemicals and dangerous GMO “foods” cause you to develop.
And, then there is the lack of safety information on consuming GMOs. All independent science makes it clear that there is no reason to believe that GMO foods are safe since their consequences are to damage the DNA OF EVERY CELL IN THE BODY, including the cells of children still unborn. All this, of course, without oversight by the FDA or USDA.
Do you know what happens when people eat genetically modified sugar? No? Neither do I. But when mammals eat GMO soy, their offspring die, or are born stunted. Their fertility is impaired, their GI tracts and kidneys and immune systems are impaired, too. So is just about every other part of their bodies. It stands to reason, of course, since the DNA and its dangerous products have never existed before and we simply lack the mechanisms to get rid of them once they are in our bodies.
Then there are super weeds and super pests and genetic contamination and…. well, it sort of makes sense to feed them to children if you are a genocidalist AND a drug company owner, don’t you think?
We rejoice that approval for GMO sugar beets was vacated (e.g., canceled) pending an environmental impact statement. But it was not vacated on the grounds that these products, once genetically modified, are unstudied, unsafe, unnecessary and must be stopped before they literally contaminate every plant and animal on earth in what is heading toward the greatest cataclysm in the history of life on this planet.
Thanks for your continuing support. Please do not forget that Health Freedom is not Free! We need your support to keep on keeping on. Click here to set up your recurring, tax deductible donation to the Natural Solutions Foundation: https://staging.drrimatruthreports.com/?page_id=189https://staging.drrimatruthreports.com/?page_id=189
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Natural Solutions Foundation’s Valley of the Moon(TM) Eco Demonstration Project
www.NaturalSolutionsFoundation.org
Valley of the Moon(TM) Toxin Free Coffee
www.ValleyoftheMoonCoffee.org
Natural Solutions Foundation’s Virtual Malls
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www.NaturalSolutionsMarketPlace.org
VICTORY! FEDERAL COURT RESCINDS USDA APPROVAL OF GENETICALLY ENGINEERED SUGAR BEETS
ORDER BANS PLANTING OR SALE OF CONTROVERSIAL CROP. COURT DENIES MONSANTO REQUEST TO ALLOW CONTINUED PLANTING
Today Judge Jeffrey White, federal district judge for the Northern District of California, issued a ruling granting the request of plaintiffs Center for Food Safety, Organic Seed Alliance, High Mowing Organic Seeds, and the Sierra Club to rescind the United States Department of Agriculture’s (USDA’s) approval of genetically engineered “Roundup Ready” sugar beets (Center for Food Safety v. Vilsack, No. C08-00484 JSW [N.D. Cal. 2010]). In September 2009, the Court had found that the USDA had violated the National Environmental Policy Act (NEPA) by approving the Monsanto-engineered biotech crop without first preparing an Environmental Impact Statement. The crop was engineered to resist the effects of Monsanto’s Roundup herbicide, which it sells to farmers together with the patented seed. Similar Roundup Ready crops have led to increased use of herbicides, proliferation of herbicide resistant weeds, and contamination of conventional and organic crops.
In today’s ruling the Court officially “vacated” the USDA “deregulation” of Monsanto’s biotech sugar beets and prohibited any future planting and sale pending the agency’s compliance with NEPA and all other relevant laws. USDA has estimated that an EIS may be ready by 2012.
Andrew Kimbrell, Executive Director of plaintiff and co-counsel the Center for Food Safety, stated, “This is a major victory for farmers, consumers and the rule of law. USDA has once again acted illegally and had its approval of a biotech crop rescinded. Hopefully the agency will learn that their mandate is to protect farmers, consumers and the environment and not the bottom line of corporations such as Monsanto.”
Paul Achitoff of Earthjustice, lead counsel for the plaintiffs, commented: “Time and again, USDA has ignored the law and abdicated its duty to protect the environment and American agriculture from genetically engineered crops designed to sell toxic chemicals. Time and again, citizens speaking truth to power have taken USDA to court and won.”
In his order, Judge White noted that USDA’s “errors are not minor or insignificant, and his “concern that Defendants are not taking this process seriously.” He also pointed out that “despite the fact that the statutes at issue are designed to protect the environment,” USDA and the sugar beet industry focused on the economic consequences to themselves, yet “failed to demonstrate that serious economic harm would be incurred pending a full economic review….”
The Court held in part:
…the Court GRANTS Plaintiffs’ request to vacate APHIS’s decision to deregulate genetically engineered sugar beets and remands this matter to APHIS. Based on this vacatur, genetically engineered sugar beets are once again regulated articles pursuant to the Plant Protection Act. This vacatur applies to all future plantings…
This is the second time a Court has rescinded USDA’s approval of a biotech crop. The first such crop, Roundup Ready alfalfa, is also illegal to plant, based on the vacating of its deregulation in 2007 pending preparation of an EIS. Although Monsanto took that case all the way to the Supreme Court and the High Court set aside part of the relief granted, the full prohibition on its planting – based on the same remedy granted here, the vacatur – remains in place. In the past several years federal courts have also held illegal USDA’s approval of biotech crop field trials, including the testing of biotech grasses in Oregon and the testing of engineered, pharmaceutical-producing crops in Hawai’i.
The Voice of Global Health & Food Freedom™
URGENT Push Back Needed to Defend Health Freedom: S.510 Remains an Immediate Threat! The Criminalization of Food Distribution Bill, S.3767 is a New and Imminent Threat!
Update: 11.17.10 – Senate may pass S.510 today! Push Back needed!
https://staging.drrimatruthreports.com/?p=7446
– FOOD FREEDOM TALKING POINTS: NO! to Food Fascism – https://staging.drrimatruthreports.com/?p=6910
– GMO DANGERS TALKING POINTS: NO! GMOs – https://staging.drrimatruthreports.com/?p=6955
The Food Freedom Amendment: https://staging.drrimatruthreports.com/?p=6999
Click Here to Take Action! Stop S.510! Stop S.3767! http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=4613
09.23.10 Update: Senate: Don’t Rush S.3767 to the Senate Floor! Support the Food Freedom Amendment Instead! http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=4878
“No provision of Federal Law giving regulatory oversight to any Federal department or agency shall be deemed to apply (a) to any home, home-business, homestead, home or community gardens, small farm, organic or natural agricultural activity, (b) to any family farm or ranch, or (c) to any natural or organic food product, including dietary supplements, as protected under the Dietary Supplement Health and Education Act of 1994.”
Health & Food Freedom Amendments Action Item: http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=3729
09.18.10 Update: Thank You Senator Coburn for Keeping a “Hold” on S.510!
https://staging.drrimatruthreports.com/?p=6719
09.10.10 – FDA/HHS “Stampede Congress” into Passing S.510 Letter!
The Empire Strikes Back… https://staging.drrimatruthreports.com/?p=6611
09.13.10 – Text and Threat of S.3767: Criminalizing the Food Trade
http://vitaminlawyerhealthfreedom.blogspot.com/2010/09/s510-companion-bill-s3767-to.html
Dr. Laibow: Stop S.510 Now!
One urgent item discussed is the faked “Food Safety” bill.
S. 510 is a lesson in the politics of persistence and perfidy.
For more than a year, the plan to capture – and kill – clean, local, organic, independent and safe farming has been wending its way through Congress. Last year, the devastating HR 2749 passed although we put up a good battle, delaying it for quite a while. However, at the end of the day, a good battle followed by a loss is still a loss. Then the field of battle shifted to the US Senate, where we’ve held the forces of Big Agra and Big Govt at bay for nearly a year… Part 1 below includes an estimate of that situation, and much more! Part 2, below, continues the discussion of strategies to defend health freedom in the USA and worldwide.
URGENT Action Item: Stop S.510! http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=4613
To read more, click here, https://staging.drrimatruthreports.com/?p=6300, and then, please come right back to watch these important videos.
1. http://www.youtube.com/watch?v=0vvdHcazFms
2 – http://www.youtube.com/watch?v=U3Kt7u-KzWc
Please support our efforts – https://staging.drrimatruthreports.com/?page_id=189
Thanks for your continuing support. Please do not forget that Health Freedom is not Free! We need your support to keep on keeping on. Click here to set up your recurring, tax deductible donation to the Natural Solutions Foundation: https://staging.drrimatruthreports.com/?page_id=189https://staging.drrimatruthreports.com/?page_id=189
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Natural Solutions Foundation’s Valley of the Moon(TM) Eco Demonstration Project
www.NaturalSolutionsFoundation.org
Valley of the Moon(TM) Toxin Free Coffee
www.ValleyoftheMoonCoffee.org
Natural Solutions Foundation’s Virtual Malls
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
Natural Solutions Foundation
The Voice of Global Health Freedom™
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Permalink: https://staging.drrimatruthreports.com/?p=6098
FDA says that autism and vaccination are not linked. They lie. Click here to demand a full scale Congressional Investigation and Hearings of Autism and other environmental diseases: http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=3688
Send this Open Letter to Codex Alimentarius demanding that your voice be heard! http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=4279
Health Freedom Needs Your Support! Set Up a Recurring Tax Deductible Donation to Keep Natural Solutions Foundation Strong! Click here, https://staging.drrimatruthreports.com/?page_id=189
Half of All FDA Approved Drugs are Quietly Withdrawn Within 5 Years of Approval
“FDA approved” drugs means “safe”, right? Clinical trials show that drugs and vaccines are safe or they wouldn’t be allowed to be marketed, right? Drug companies have to report what actually happens in a clinical trial, right? Once a drug is approved by the FDA for market release it stays available for a long time, right?
Lethal and potentially lethal side effects from FDA approved drugs are rare, right?
The answer to these questions is one big collective, “NO!!!!!”
Here are the facts: Drug companies are free to suppress negative clinical trial information with impunity. That is not how the system is designed to work, at least on paper, but it is the way things work in the real world.
Drugs, all drugs and vaccines, enter Phase IV clinical trials when they are released for general use. Depending on how many people they kill, maim, blind or cause to suffer once doctors start prescribing the drug for whatever the FDA has approved it for, although they can use the drug for anything they want to (called “off label prescribing”). Even the callous, corrupt and conflict-of-interest-riddled FDA withdraws approximately 50% of all approved drugs within 5 years of approval because they are just too toxic to continue on the market.
How did they get approved in the first place? Well, as you will see when you read the articles below, drug companies disregard the requirements to be honest in reporting data as they choose. Given that it can cost up to a billion dollars (yes, you read that right, a billion US dollars) to research a drug and bring it to market, there is an enormous amount of pressure to get the drug into the patients’ hands by putting it in the doctor’s mind and getting it onto his/her prescription pad – no matter what.
One of the may ways drug companies accomplish what they want – drug sales, is to lie about how many people die or drop out in drug trials.
Another way is by literally purchasing the decision-makers for stock options, research grants and other inducements plucked fresh from the abundant and ever self-replenishing FDA Corruption Tree.
The results? Pharmaceutical Mayhem.
Drugs are the leading cause of death in the US and every other “developed” nation. But, not to worry, the FDA is on the job.! Oh, good. I was worried there for a moment!
You know, insultingly enough, the FDA expects you to believe that these deadly drugs released to the public to see what happens (and what happens is mayhem and murder much of the time) could possibly be an accident? Neither do I. Remember, these same drug companies are big players at Codex. They are the heirs and legatees of the German genocidalists who created Codex Alimentarius, now degrading the world’s food supply as a stepping side to “the Great Culling”, the death of 90% of the world’s population.
Bottom line, from where I stand? If you are not in an Emergency Room, there is, in my experience and belief, no reason to take drugs when inexpensive, gentle, effective and powerful natural options exist through orthomolecular medicine, homeopathy, naturopathy, chiropractic, acupuncture, Bio Acoustics, NeuroBioFeedback, Frequency Medicine, chelation, detoxification and a host of other helpful, safe techniques await your decision-making. But that is the very point, isn’t it? If you are an immensely powerful drug company and you know that your drugs are toxic, expensive, dangerous, poorly conceived and poorly tested, grossly dishonestly marketed what would you do? Jeopardize your cash bonus and tell the truth, wasting a billion bucks? Probably not. Probably you would do what the drug companies (and the BioTech companies which make GMOs and are usually one and the same as the drug companies!). You would lie, and lie big!
“These drugs are safe.” “The clinical trials show it.” “People do not get sick from our drugs.” “We followed the rules.” “You can trust us!”
Stuff and nonsense!
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Valley of the Moon™ Eco Demonstration Project
www.NaturalSolutionsFoundation.org
www.InternationalDecadeofNutrition.org
Valley of the Moon Coffee
www.ValleyoftheMoonCoffee.org
NSF Virtual Malls
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
The Dr. Rima Network: www.DrRima.net
Food Freedom eJournal
www.FoodFreedomeJournal.org
Ana Cantu was a Human Guinea Pig in a Drug Trial for $4,800
Vera Hassner Sharav
Monday, 26 July 2010
“The study started out with 20 subjects…For about a week there were 14 subjects. Then they started dropping…Now, we’re down to 7.”
Below, a testimonial by Ana Cantu who was one of the healthy volunteers –“a human guinea pig” as she describes herself– in a month long study that tested the effects of Norvir, an HIV drug made by Abbott Laboratories, when coupled with the antidepressant Wellbutrin, made by GlaxoSmithKline.”
Her first-hand experience provides insight about the immense “pressure for positive results in clinical trials,” the level of discomfort a human subject is expected to endure from the adverse effects of the tested drug (or combination of drugs), and the dilemma for drug manufacturers whose drug causes adverse effects so severe, the test subjects in pre-marketing trials drop out in droves. The FDA accepts study results–even if only 7 of 20 subjects complete the study. Companies are loathe to scrap a negative study: they hold on to the last 7 subjects despite severe adverse effects. The “volunteers” suffer for the payment which they would forfeit if they quit.
Ana describes how and why corporate sponsors–in her case, GSK and Abbott Labs–conceal adverse event data that may damage a drug’s chances for approval.
Despite federal law requiring companies to fully disclose to the FDA all adverse events in pre-marketing clinical trials, drug companies have repeatedly violated the law with impunity: they have failed to include in their submission of data to the FDA, the worst adverse events suffered by subjects who, as a result, dropped out of the trials.
Her observations, published in The American Statesman (below) are disturbing and insightful:
“The study started out with 20 subjects, but 6 were eliminated during the in-patient stay by the drug company sponsoring the trial for various reasons (including drinking caffeine within 24 hours of check-in). For about a week, there were 14 subjects. Then they started dropping. The first one to go was a girl with a pronounced Texas twang named Denise, who had severe jaw and tooth pain. Then extreme nausea and emesis (the clinical term for vomiting, I discovered) claimed April. Jo Kay, Paula, Amy, Alyssa and Carrie went one after another. Now we’re down to 7.”
Ana experienced severe black outs–clearly an adverse effect of the experimental drug–but she was kept in the trial against her best interest:
“The day got off to a bumpy start when I started to black out while reporting my side effects. Darkness closed in from my peripheral vision and then I saw nothing but big colored spots.
“That morning, we were standing around in the cafeteria waiting to dose. All of a sudden, I couldn’t see and lost the ability to balance. If I hadn’t been standing between two of my fellow subjects, who grabbed me and held me up, I would’ve slammed into the floor. I knew I hadn’t fainted; I could still hear just fine, but all I heard was chaos as everyone around me freaked out. I dropped into the nearest chair and put my head between my legs while the study coordinator called the on-site paramedics. While the coordinator frantically called the staff doctor, a paramedic checked and re-checked me. I did fine as long as I wasn’t on my feet for too long. The doctor cleared me to keep dosing.”
Ana explains why her continued “participation” in the trial–disregarding the danger the black outs posed to her well-being–was to accommodate the sponsoring company’s need to maintain a minimum of 7 subjects in the trial:
“The drug company had a dilemma. To submit trial results to the FDA, the study couldn’t fall below seven participants. But, unfortunately, one showed signs of serious side effects and if those results were submitted, approval was highly unlikely. If my results were dropped, the FDA would never know about the problem and the drug company could start fresh with a third trial. However, the first clinical trial had to be scrapped because too many subjects dropped out as a result of their side effects, and it looked like the second study could soon follow the same path. To gather enough healthy volunteers who fit the protocol for a third trial would require a lot of time and money, and it wasn’t something the sponsor was willing to do. So, in the end, my results and I stayed in the study.”
“Because the trial ended with the magic number of seven volunteers, the results could be submitted for review and the FDA had the opportunity to see the data. But what happens in the trials in which drug companies drop some of the subjects with the worst side effects?”
Ana Cantu’s first-hand experience confirms the finding reported by FDA’s safety officer, Dr. Thomas Marciniak, who analyzed the raw data from GSK’s Avandia trial, and found that the company concealed from the FDA the worst adverse event data, resulting in its approval precipitating preventable heart attacks and deaths.
An editorial in today’s New York Times, calls upon the FDA to revoke its questionable approval of Avastin for breast cancer because it failed to extend patients’ lives while it caused serious side effects. The drug had gained “accelerated approval” without adequate testing.
~~~~~~~~~~~~~~~~~
Cantú: Anatomy of a drug trial
By Ana Cantú
AMERICAN-STATESMAN Friday, July 23, 2010
Exactly five years ago, in exchange for the most miserable month of my life, I got paid $4,800 to test the effects of a drug made by GlaxoSmithKline.
You know where you’ve heard the name GlaxoSmithKline recently, right? That’s the company on the verge of losing the approval of the Food and Drug Administration for the diabetes medication Avandia after regulators discovered omissions in a key clinical trial report. On Wednesday, the FDA ordered Glaxo to stop enrolling people in another Avandia trial.
According to a review reassessing the drug’s safety by the FDA’s Dr. Thomas Marciniak, a number of patients taking Avandia appeared to have serious heart problems that were not counted in the study’s tally of adverse events, otherwise known as side effects.
Such repeated mistakes “should not be found even as single occurrences” and “suggest serious flaws with trial conduct,” he wrote.
It can cost hundreds of millions of dollars — in some cases, close to a billion — in research and development for a drug company to secure FDA approval.
By the time a drug gets to point where it can be tested in humans, the pressure for positive results in clinical trials is immense. And I found that out first-hand when as one of the healthy volunteers — a human guinea pig — in a study that tested the effects of Norvir, an HIV drug made by Abbott Laboratories, when coupled with the antidepressant Wellbutrin, made by GlaxoSmithKline.
In exchange for that $4,800 paycheck, I spent about a month going in and out of a blocky silver building in an office park not far from Austin-Bergstrom International Airport, the site of a contract research lab that conducts medical studies.
During the lab’s second clinical trial of the Norvir-Wellbutrin combination, which I chronicled in a personal blog, I was known only subject No. 40.
July 12: I check in tomorrow for 4 days. I’ll be taking an antidepressant and an AIDS drug in combination for about a month.
July 13: The facility is freezing. We’re still waiting on blankets. I should’ve brought a hat and gloves. You can tell the people who do studies regularly by their baggage — they bring extra pillows and blankets and huge rolling suitcases. The building is pretty new and it’s painted in all kinds of “modern” colors like bile, which complement the black-and-white tiled floors nicely. Subjects sleep 8 to a room in bunk beds, though there are only 3 people in my room. …
My first dose of Wellbutrin is tomorrow. I hear it gives you crazy dreams.
July 14: I’ve been stuck so many times today I feel like a junkie. I had to be up by 6:12 a.m. to check vital signs and get a pre-dose blood draw. Then I had breakfast, which I had to finish: two potato, egg and cheese tacos with pico de gallo and a carton of 2% milk, which I don’t like. I took the Wellbutrin at 7:27, so precisely every hour after that I’ve been having blood drawn. For the rest of the day, it’s blood draws only every 2 hours. I carry around a clipboard that has all my procedures and meals scheduled — everything has to be done exactly as it says on the sheet or they can dock pay off your study-completion bonus.
Amusing sign near the toilets: Please do NOT use cellphones in urine monitoring stations.
July 15: Dinner was decent — teriyaki chicken, rice, salad with Italian dressing, a hunk of zucchini bread and a sugar cookie. I tried the cookie and didn’t like the aftertaste so I hid it in a spare napkin and arranged everything else on the tray to conceal it. The cafeteria workers check how much of our food we eat — we’re supposed to finish at least 50% of everything. Sometimes it’s hard, like with yesterday’s trail mix. I hope we get a good snack, which I will take my first bite of at precisely 9:32 p.m.
About half of the subjects have done trials before and say that ours isn’t so bad, even with all the blood draws. Apparently, there are some where you have them every 15 minutes. …The people who usually play Monopoly switched to Uno.
July 18: Yesterday I had my first bad blood draw.
July 20: Tomorrow I start my doses of Norvir, the AIDS drug. Fun, fun.
July 23: I started on the AIDS drug on Thursday — 300 mg twice a day. The dosage gets upped to 400 mg tomorrow. I don’t feel bad yet, though I’m sleeping less than normal. And today my stomach objected to the egg facsimile we had to eat.
July 25: I was pretty excited that I didn’t get sick after my dosings. … I think the secret is to not drink the milk. And not to eat more than 50% of the food. I’m becoming an expert in artfully rearranging things on my plate so it looks like I’ve eaten. They (try to) make us eat after taking the giant AIDS pills, but since we get the same few meals over and over, it’s gotten really hard to do. Plus, there’s a chance you’ll get sick after so you really don’t want to see nasty food twice, if you get my meaning.
July 28: I discovered that I feel better if I don’t eat after taking the horse pills. This morning, I refused to eat the breakfast tacos and felt fine. So I followed the same strategy at dinner — I did eat the peas and carrots and drank some caffeine-free root beer, but most of the meal was untouched.
Over the course of the trial, as a result of a near-constant state of nausea, I lost about 10 percent of my body weight.
To keep up my strength, for lunch, I’d go to a fast-food restaurant and order the heaviest combo on the menu (double bacon cheeseburger, fries and a huge non-caffeinated beverage) and eat as much as I could before I started to feel sick again.
Every night, insomnia cut my sleep to three hours.
Aug. 1: The study started out with 20 subjects, but 6 were eliminated during the in-patient stay by the drug company sponsoring the trial for various reasons (including drinking caffeine within 24 hours of check-in). For about a week, there were 14 subjects. Then they started dropping. The first one to go was a girl with a pronounced Texas twang named Denise, who had severe jaw and tooth pain. Then extreme nausea and emesis (the clinical term for vomiting, I discovered) claimed April. Jo Kay, Paula, Amy, Alyssa and Carrie went one after another. Now we’re down to 7. In what I view as biological injustice, none of the males have shown noticeable symptoms.
Aug. 2: I had to go see an opthamologist today, just for my safety, since I reported a migraine with aura a few days ago. Unfortunately, I’m fine. Curses. I was hoping I could get medically excused from the study — that way I’d still get paid. But it looks like I’m going to have to finish it. Only 10 more days of dosing to go. My current side effects include oral numbness and tingling in my extremities.
Aug. 6: It’s another day in lockup: cloudy skies (I think) and cold air conditioning. The day got off to a bumpy start when I started to black out while reporting my side effects. Darkness closed in from my peripheral vision and then I saw nothing but big colored spots.
That morning, we were standing around in the cafeteria waiting to dose. All of a sudden, I couldn’t see and lost the ability to balance. If I hadn’t been standing between two of my fellow subjects, who grabbed me and held me up, I would’ve slammed into the floor. I knew I hadn’t fainted; I could still hear just fine, but all I heard was chaos as everyone around me freaked out. I dropped into the nearest chair and put my head between my legs while the study coordinator called the on-site paramedics. While the coordinator frantically called the staff doctor, a paramedic checked and re-checked me. I did fine as long as I wasn’t on my feet for too long. The doctor cleared me to keep dosing.
A few days after my first blackout episode, during a scheduled outpatient visit, one of the study coordinators said I had to be examined by the on-staff doctor. “Why?” “The sponsor is concerned about your side effects,” she said.
The drug company had a dilemma. To submit trial results to the FDA, the study couldn’t fall below seven participants. But, unfortunately, one showed signs of serious side effects and if those results were submitted, approval was highly unlikely. If my results were dropped, the FDA would never know about the problem and the drug company could start fresh with a third trial. However, the first clinical trial had to be scrapped because too many subjects dropped out as a result of their side effects, and it looked like the second study could soon follow the same path. To gather enough healthy volunteers who fit the protocol for a third trial would require a lot of time and money, and it wasn’t something the sponsor was willing to do. So, in the end, my results and I stayed in the study.
Aug. 21: So yesterday I had the exit screening/physical for my drug study. I had to have my blood pressure checked 3 times because it was low, even for me. The paramedic checked me, but I was asymptomatic. She asked how I was feeling. “Fine, especially now that I’m off the drugs.” She said, “Well, it was for the good of mankind.” “I guess … and the money.”
Because the trial ended with the magic number of seven volunteers, the results could be submitted for review and the FDA had the opportunity to see the data. But what happens in the trials in which drug companies drop some of the subjects with the worst side effects?
Actually, we’ve seen what happens — with Avandia.
~~~~~~~~~~~~~~~~~~
When a Drug Fails
THE NEW YORK TIMES July 25, 2010
The flameout of an enormously expensive drug to treat advanced breast cancer will pose a critical test for the Food and Drug Administration. Will the agency have the courage to reverse course when a medical treatment that it approved based on preliminary evidence flops badly in follow-up studies?
Two years ago, the F.D.A. gave Avastin, which is made by the Genentech unit of Roche, “accelerated approval” as a treatment for breast cancers that have spread to other parts of the body. Such cancers are essentially incurable so the best that current treatments can do is extend a patient’s life.
The hurry-up mechanism allows approval of a drug that has not yet been proved safe and effective in thorough clinical trials but has shown promise that it might benefit patients with life-threatening diseases. Rather than make such patients wait, they are treated with the drug while the manufacturer completes additional tests.
When Avastin was granted “accelerated approval” to treat advanced breast cancer, the primary evidence was a single clinical trial. It found that Avastin, when used with another drug, slowed progression of the disease but did not significantly extend patients’ lives.
Now two follow-up trials by the manufacturer have failed to confirm even those meager gains. In the initial trial, Avastin held tumor progression at bay for five and a half months. In the two new trials, pairing Avastin with different chemotherapy drugs, the delay in tumor worsening was much shorter: up to three months in one trial and less than a month in the other. The Avastin combinations also caused serious side effects.
Britain’s National Institute for Health and Clinical Excellence, a pace-setter in evaluating medical advances, issued draft guidance this month against using Avastin for advanced breast cancer patients in the National Health Service. It called the clinical trial data “disappointing” and the cost “too high for the limited and uncertain benefit it may offer patients.”
By a 12-to-1 vote last week, an F.D.A. advisory committee quite sensibly urged the agency to revoke Avastin’s approval for breast cancer. That would not affect its other approvals, gained through the standard regulatory process, for treating colon, lung, kidney and brain cancers. Avastin would remain available to doctors for off-label use against breast cancer. Many insurers, however, might refuse to cover an unapproved use.
The cost of Avastin has always seemed outrageously high for the medical benefits it confers. The wholesale price for a typical breast cancer patient is about $88,000 a year. Genentech has been capping annual spending at $57,000 for patients with incomes below $100,000.
The F.D.A. has rarely removed drugs that were given accelerated approval and sometimes has failed even to compel completion of follow-up studies. But there are signs it may get tougher. In June, the agency finally forced a leukemia drug off the market that had been given accelerated approval a decade ago, after a long- delayed follow-up study showed no clinical benefit and an increased risk of death. With Avastin, the follow-up studies were completed in a timely manner — with such meager results that withdrawal seems the right response.
http://www.theoneclickgroup.co.uk/news.php?start=3760&end=3780&view=yes&id=5045#newspost
Natural Solutions Foundation
The Voice of Global Health Freedom™
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Saturday, July 10, 2010
Permalink: https://staging.drrimatruthreports.com/?p=5887
Don’t Miss Dr. Rima on Blogtalk Radio Sunday Night!
Final Report from Codex - Is YOUR death their goal?
Interview with Vaccine Exemption Lawyer.
The Doctor takes your questions.
9 PM EDT – Midnight
More here:
https://staging.drrimatruthreports.com/?p=4850
In This Issue:
The Doctor Is In: “Codex is Certifiably Insane!”
The BeyondOrganic™ Marketplace has Reopened!
Find Out About Our Next Guest on the Dr. Rima Reports
Two Codex Blog Links You MUST Click!
Current ‘Must Take’ Action Items
Dr.Rima Recommends:
The Dr. Rima Institute’s Grand Opening, August 7/8, 2010
You’re Invited: Volcan, Panama
https://staging.drrimatruthreports.com/?p=5838
Breaking News!
FDA Approved Another Drug Now Shown Dangerous!
Is this “News” or just “Business as Usual” for the FDA?
Once again, the FDA had approved a drug but now “found a dozen instances in which patients taking [drug “A”] appeared to suffer serious heart problems that were not counted in the study’s tally of adverse events. ” – http://www.nytimes.com/2010/07/10/health/10diabetes.html?
We Attended the Codex Meeting:
We came. We saw… US govt conquered.
And that’s not good for Americans or the World!
Dr. Rima’s Daily Video Reports from Codex
https://staging.drrimatruthreports.com/?p=5821
Foundation Targeted by Codex Agents!
An Open Letter to the Codex Commission from Gen. Bert
https://staging.drrimatruthreports.com/?p=5900
US Out of Codex Video
https://staging.drrimatruthreports.com/?p=5509
http://salsa.democracyinaction.org/o/568/t/1128/questionnaire.jsp?questionnaire_KEY=1042
Donate to Defray Costs at Codex:
https://staging.drrimatruthreports.com/?page_id=189
Your generosity and support sends Natural Solutions Foundation to a variety of Codex meetings around the world. Right now General Bert and I are in Geneva Switzerland.
We left our home at the Valley of the Moon Eco Demonstration Project in Volcan, Panama, www.NaturalSolutionsFoundation.org, to get on a plane to Panama City, then another one to Madrid and another one to Genva two days ago so that by the time we reached Switzerland we had not slept for about 48 hours. Why didn’t we take a quicker, more direct route? Because neither General Stubblebine nor I am willing to expose our bodies to the radiation hazard of full body scanners and neither Madrid nor Geneva airports use full body scanners.
Dr. Rima continues to write about the the machinations at Codex here:
https://staging.drrimatruthreports.com/?p=5821 and here is part of what she had to say:
“…Why the Codex Apple? The apple suggests wholesome food.
Nothing could be further from the truth. As if to underscore the destruction of the world’s food supply, the 33rd Meeting of the Codex Alimentarius Commission, July 5-9, 2010 (Geneva, Switzerland) approved a standard for apples which permits not more than 5% of the apples to be composed of ACTIVLY FEEDING INSECTS!
When India and other countries protested that this unprecedented approval of filth as “food” would lead to poor quality and inedible food being dumped in the poorest nations, the Secretariat clarified that this standard permits FEEDING insects, not PEST insects. Despite the strong protest expressed by numerous countries, large and small, the US, EU, Argentina, Brazil, Australia and New Zealand, the countries least likely to wind up with these insects on their dinner plates, bulled their approval through with the complicity of the Codex Commission Chairperson, the US’s Karen Hullebeck.
Everything else done by this Codex session continues to degrade the world’s food supply despite the continuing, but continually ignored, protests of the developing world.
Have An Apple, My Brown-Skinned Friend!”
We got to Geneva and continued our preparation for the meeting. You see, in order bring you intelligent, meaningful and precise information in our daily video and written reports and later create meaningful strategies to deal with Codex and its dangers, we need to do a major amount of planning and preparation.
Codex is designed to be overwhelmingly complex, detail driven and difficult to comprehend because the technical level of the considerations is so enormously demanding if you are going to understand it all. Delegates are just supposed to be so overwhelmed that they simply sink into a lulled position in which whatever the US or EU says is what they go along with, sort of like the courtiers just letting the red queen do what she likes in Alice and Wonderland because it is so much easier and safer.
But at Codex, as in so many other urgently important situations, the devil really IS in the details. Consider:
There are 15 Committee Reports to be studied from major codex Committees (http://www.codexalimentarius.net/web/archives.jsp) for the Codex Alimentarius Commission (CAC) session starting on Monday, July 5.
The Report of the Codex Executive Committee has 28 pages
The Committee on Food Labeling has 58 pages
The Committee on Contaminants in Foods has 69 pages
and so on through the 15 committees presenting their items for discussion at the CAC.
Dr. Rima’s Daily Video Reports tell the whole story:
https://staging.drrimatruthreports.com/?p=5821.
Potentially buried in each one of the clauses, phrases, reports and agenda items is a time bomb that can, despite its innocuous language, kill people through the implications and permissions granted via its legalese.
Nutrient Reference Values (NRVs) and GMO labeling are excellent, but by no means unique, examples. Both of these issues are highly technical and both, if carried out as the US desires, would lead to highly undesirable outcomes. NRVs are daily intake values of nutrients so low that they actually introduce and make permanent, the under-nutrition which WHO and FAO point out as the primary cause of the non-communicable, preventable, degenerative killer diseases: cancer, cardiovascular disease, stroke, diabetes and obesity. Misleading consumers into believing that their processed food provides adequate levels of vital nutrients, the NRVs are both a biochemical absurdity and an atrocity since they will, through their use on labels, lead people to believe that since their food is providing most or all of the NRVs, it provides the nutrients they need for a healthy life.
NRVs have been winding their way through the Codex Committee on Nutrition and Foods for Special Dietary Uses (CCNFSDU) and the Committee on Food Labeling (CCFL). When South Africa was discussing them in 2005 at CCNFSDU, Dr. Grossklaus, the Chairman cut the delegate off at the knees when she mentioned “optimal nutrition” and said “It would be nice if Codex were about nutrition, but it isn’t. It’s about trade!” But most delegates have no idea what biochemical individuality is about, why high potency nutrients save lives, money and misery and the discussions must include the technical issues of the Codex texts and committee which are dealing with NRVs, their status in the CAC, etc. To learn more about where this nutrients as toxins, nutrients as controlled substances, idea in Codex, click here to watch “Nutricide”: http://video.google.com/videoplay?docid=-5266884912495233634#
.
GMO labeling is another example, as is whether Codex should define consensus or a code of ethics for codex participants. In these discussions and decisions, information lies which could, going in one direction, change history and survival for good and, going in the other direction, could do exactly the opposite.
Each Agenda Item rests on a multi-year background with a huge pile of data and debate behind it. Having that perspective is essential to informed, effective dialogue with the delegates at Codex and in their home countries. And that is what we do at Codex! We take your interests, and those of well-nourished, autonomous, food independent people and “bang them against” what Codex is doing. The lives of food producers, food consumers and the planet turn on these tiny nuances since all of the Codex documents are written in such a way as to lull you into a fluorided haze of complacency. There is, however, nothing to be complacent about.
There is also nothing worth participating in at Codex. It is my contention that the United States needs to get out of Codex and do it now. We will lose nothing and grain a great deal, I believe, by loosening the hold that we have allowed the World Trade Organization, WHO, to place on us through trade agreements that can only inevitably degrade our food and our health unless we follow the Codex Two Step Process, as other nations have done successfully. If we were out of Codex, I believe that two things would happen:
First, it would be a great deal easier for interested parties to apply pressure to force the US to deviate from the Codex guidelines and standards since we would not have teams of experts ramming these guidelines and standards through Codex and, second, we would not be twisting and distorting the entire Codex process, making the decisions that the US wants, not the ones that protect the farmers, the consumers and the earth. By the way, the Developed World is one of the major consumers of third world-produced toxic food. Here is the link to my video:
https://staging.drrimatruthreports.com/?p=5509
and here is the link to the Survey in which you tell us if you think that the US should get out of Codex:
http://salsa.democracyinaction.org/o/568/t/1128/questionnaire.jsp?questionnaire_KEY=1042
There are at least a hundred equally vital items before the CAC this week. They would be far better decided by the national competencies of the countries rather than by the “bully of the class” threatening the other kids in the class with the active and vigorous help of the corrupt and self interested “teacher”, WHO, a corrupt and genocidal organization which acknowledges that it wants to see the population of the earth reduced by a minimum of 80%, better 90%!
So what we do is prepare for the topics of greatest interest to you and to the developing world’s delegates, mingle with delegates and share our perspectives on these topics and provide leadership for dissent strategies. Then, very importanty, we offer them information on how they can increase crop yield, decrease food born illness, and, in reality, actually accomplish exactly what Codex says it is about.
And we report. After each day’s meetings, we make sure that you know what the highlights (and low points) of the day’s proceedings have been, what they mean for you, what they mean for the dangerous forward movement of “HARMonization” by the US and how to protect ourselves, our health and our health freedom.
Attending Codex is really hard work. We do it for you, with your support because it is hugely important. At the end of a Codex meeting we are exhausted. Then we fly home to Panama to put the things we are teaching the developing world into practice.
Our Natural Solutions Center will be opening at the Valley of the Moon™ Eco Demonstration Project in Volcan, Panama, on August 7/8, 2010. You are invited. Please join us for this important step forward. You can see the health protocols that we plan to offer if you visit
www.DrRima.net. And you can be with us for the initiation of what is, in essence, the exact opposit of what Codex is about. We’ll be living, teaching, sharing and creating clean food and vital freedom through education and dissemination, demonstration and direction.
For more information on the Valley of the Moon™ Eco Demonstration Project, how you can participate in it, live there, work there, safeguard your retirement income there and otherwise be a huge part of this innovative freedom project, please visit www.NaturalSolutionsFoundation.org. And if you would like to join our very active NSF-Panama Forum on Yahoo.com, please visit
http://tech.groups.yahoo.com/group/NSF-Panama/join
to become part of this vital community while you still can.
And, oh, yes, don’t forget that the limited supply of our amazing Valley of the Moon™ Coffee is available for you now. If you want premium Panamanian Highland coffee grown without a single chemical contaminant, you need to place your order before it is all gone. Don’t forget your corporate gifts this holiday season and your personal ones. Order now and we will make sure that your recipients are not left out in the gift-giving cold this year! Make your tax deductible donation and get what we believe you will agree is the best coffee you have ever tasted at www.ValleyoftheMoonCoffee.org
.
Because of high winds, we had to cut down 80% of our plants to allow them to regrow so this scarce beauty of a coffee is even scarcer. Our harvest is magnificent, but the best coffee in the world, and the cleanest, is even more rare than last year! We have not raised the price of a donation, but make sure you get as much as you need before there is no more left this year.
You will be astounded by the events that have been taking place at the Codex meeting… and, of course, we’ve been isolated and restricted by “The Powers That Be” — but worry not, our voices are being heard.
Please take a look at Dr. Rima’s Daily Codex Videos at:
https://staging.drrimatruthreports.com/?p=5821.
And two hard-hitting blog entries:
Gen. Bert on Science and Codex – https://staging.drrimatruthreports.com/?p=5874
Dr. Rima on Codex and Death – https://staging.drrimatruthreports.com/?p=5879
.
Once you’ve taken a look at the videos and blog entries, I am sorry to say that you are likely to agree with Dr. Rima: “Codex is certifiably insane… so it’s time for the US to get out of Codex since the presence of the Federal agencies and their Big Biz controllers makes Codex more insane – and more dangerous – every year.”
And, as hard as it is on us, thank you for sending us to Codex. We still need your donations to finish defraying the cost (Geneva, Switzerland, is a very expensive place!) so please, please help today:
https://staging.drrimatruthreports.com/?page_id=189
Yours in health and freedom,
Dr. Rima and General Bert
Rima E. Laibow, MD
Medical Director
Maj. Gen. Albert N. Stubblebine III (US Army, Ret.)
President
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NEW MARKETPLACE HAS RE-OPENED!
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A Great Way to Support Your Health and
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Listen to the Dr Rima Reports
Sunday Night Starting 9 PM Eastern to Midnight…
www.BlogTalkRadio.com/FreedomizerRadio
1. 9 PM: Dr. Rima and Co-Host Ralph Fuectola address this week’s health freedom news and rumors — We’ll discuss the heath freedom information and sort out the disinformation for you…including
What to Expect from the Codex Meeting in Geneva…
2. 9:15 PM to 11 PM Eastern Time: Dr. Rima interviews Allan J. Phillips JD. Counsel Phillips is an expert in several areas of law that are important to Health Freedom, including vaccine exemptions. This wil be a very interesting and informative program!
https://staging.drrimatruthreports.com/?p=4850
3. 11 PM to Midnight Eastern Time: The DR. Is IN! Dr. Rima takes your health and health freedom questions. Ask your questions by
a. Email to Dr.Laibow[at]gmail.com (“QUESTION” as the subject line, please)
b. Chat (join chat community at www.BlogTalkRadio.com/FreedomizerRadio)
c. Phone using our call in number, 347.324.3704
Please get as many people as you can to join our chat room since potential supporters monitor the number of people in the chat room. The more, the better!
Details & Listening Instructions here:
https://staging.drrimatruthreports.com/?p=4850
Listen to Dr. Rima on Cock of the Talk with Fred van Liew, www.dcix.fm, Thursday Morning 9-11 AM Central Standard Time
Blog Links YOU MUST CLICK On and Read!
Please read and forward as widely as you can!
Gen. Bert on Science and Codex – https://staging.drrimatruthreports.com/?p=5874
Dr. Rima on Codex and Death – https://staging.drrimatruthreports.com/?p=5879
And these from last week…
Petrochemical Detox Information That Could Save Your Life:
If the Gulf Disaster is Making You Ill, You MUST READ This and Pass It Along!
https://staging.drrimatruthreports.com/?p=5783
How to Create a Food Supply 101: Valley of the Moon™ Moves Forward!
https://staging.drrimatruthreports.com/?p=5745
Are YOU Making a Difference?
https://staging.drrimatruthreports.com/?p=5746
Attention Rotary Clubs! Before You Help Distribute Polio Vaccines, CDC Says Polio Vaccine Causes Polio!
https://staging.drrimatruthreports.com/?p=5729
Current Action Items
Each of These Action Items is Vitally Important.
Please Take Once For EACH MEMBER of your Family,
Then Forward to Your Whole Contact List
Include a brief note saying this is important to you and you are sure that it will be to the other person and urge them to take action and forward widely
- President Obama: Allow Natural Solutions!
- Food & Health Freedom Action Items and Video…
- Support Health Freedom of Speech Acts!
- Demand Congress Investigate Autism and Environmental Toxins!
- New “Thank You Senator” for stopping S510! Educating Congress: Do Not Suppress Organic and Small Farmers & Ranchers; Natural Food Products…
- Health Keepers Oath
Dr. Rima Recommends:
THE DR. RIMA INSTITUTE
The Valley of the Moon™ Eco Demonstration Project’s Natural Solutions Institute, which we call the “Dr. Rima Institute” for short, is about to open in the beautiful, bountiful, temperate highlands community of Volcan, Panama on August 7-8, 2010 and you are invited!
Your invitation: https://staging.drrimatruthreports.com/?p=5838
You can read more about this long-awaited opening, follow our progress (we will be posting photos and videos!) at the Dr. Rima Network web site:
where you will also find a description of many of the natural protocols to be offered at the Institute and some of the products we love
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Valley of the Moon™ BeyondOrganic Coffee
Supplies are Limited for this Artisenal, Hand Picked and Roasted Coffee. Place your gift orders now for yourself and friends.
Valley of the Moon™ Coffee make a wonderful corporate gift for friends, colleagues and clients. Gifts say a lot about the giver. Your impeccable taste is revealed when you give GMO-Free, Toxin-Free, Non Toxic Valley of the Moon™ Coffee This Year!
Valley of the Moon™ Coffee:
I Promise You:
You Have Never Had a Better Cup of Coffee!
Non Toxic, Clean, Beyond Organic… Powerfully Antioxidant…
Order Yours Now!
Every Bag Valley of the Moon Coffee Supports your Physical Health and supports the Natural Solutions Foundation at the same time!
What? You’re Still Drinking Ordinary Chemical Coffee?
You Have No Idea What You Are Missing!
Health Freedom’s Own Coffee, Valley of the Moon Coffee, Will Delight You, While You Support the Natural Solutions Foundation With Your Morning Java! Make a donation and get your coffee. Once you taste this exceptional brew, we know you will love it! Write to us at dr.laibow@gmail.com to let us know your experience drinking Valley of the Moon Coffee. We are confident that it will the finest cup of coffee you have ever tasted in your life, bar none!
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Cognitive Enhancement Nutrition:
Empower Your Mind!
Dr. Rima and Gen. Bert love these leading-edge products…
Control your own mind! Feed your brain what it needs for discernment and acuity…
“These are the times that try men’s souls…” Are you ready?
Dr. Rima has designed a third, very special
Dietary Supplement Mind Enhancement Pack!
To learn more, or to try the products, go to:
Cognitive Enhancement
“News & Specials” list the three Dr. Rima Packs
For more Details about the Packs:
https://staging.drrimatruthreports.com/?p=4558
You know there is a battle going on for your mind (or maybe against it!). Part of the Globalist Agenda to reduce human population and restrict our freedoms goes on in our own heads, as we are subjected to a level of propaganda that can only be termed “mind controlling.” Its success depends on making sure that we are dumb, dull, deluded and distracted….
See the video interview with Dr. Rima and Gen. Bert
http://www.youtube.com/v/_FL3SKYVEwE
Let me quote General Bert, “‘Focus and clarity’ were the words Ralph used to describe the Cognitive Enhancement nutrients, and that is exactly what I experienced. Both my long and short term memory are enhanced by these products and my thinking processes are noticeably sharper. I am very impressed and intend to continue using them.”
There are numerous smart nutrients, but few of them, working synergistically, have the capability of doing what these products actually do. In this battle to take back our food, our health and our freedoms, we must all be as mentally sharp as possible. That is why the genocidal elitists want us under-nourished and unable to think. I was so impressed with these products that I immediately began to study them and their impact. I researched the ingredients and am satisfied that there is no indication of a lack safety when used as directed. That’s when I decided to create combination packs that would support mental function without agitating; would enhance cognition without later let-down. Dr. Rima
If you’ve had problems placing orders for these extraordinary nutrients, we’ve set up a special email address for you to use; just email your contact information and we’ll have you called back right away!
brians@biologicsnutra.com
Natural Solutions Foundation has no corporate sponsorship. YOU are our ownly sponsors, but the goods and services come from companies who believe in what we are doing. Every sale helps to support the Foundation and move our health freedom actions forward. We urge you to patronize these mission-driven malls where you will find outstanding ways to support and be supported as free men and women!
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
Valley of the Moon™ Eco Demonstration Project
www.NaturalSolutionsFoundation.org
Nano Silver: The Universal Antibiotic
www.Nutronix.com/naturalsolutions
StemEnhance: Increase Your Stem Cell Population Naturally
http://www.wealthbuilderssystem.com/site/index.asp?DL=140935&page=103264&ad=0
Detox Your Cells Naturally
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