Health Freedom Needs Your Support! Set Up a Recurring Tax Deductible Donation to Keep Natural Solutions Foundation Strong! Click here, http://www.healthfreedomusa.org/?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Half of All FDA Approved Drugs are Quietly Withdrawn Within 5 Years of Approval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
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.
Cassandra, the daughter of King Priam and Queen Hecuba of Troy was cursed by Apollo, whom she offended, with always being right but never being believed. She warned her father not to open the gates to the Trojan Horse but no one listened. The horse was brought in and, the story goes, in the dead of night, its huge belly was opened and the warriors hidden within destroyed Troy. Being right did not make Cassandra happy.
Being right does not make me happy when I am writing about things like deceiving, diagnosing and drugging an entire population for the benefits of anyone but the patient.
Being right when I wrote, decades ago, that the use of psychiatric drugs, especially in children, was a disastrous, brain-damaging and insane social and medical policy. These drugs are untested, toxic and will create a society of pharmaceutically damaged people rather than ill people being well treated. Being right when I said that the Diagnostic and Statistical Manuals for Psychiatry were dangerous and would lead to the expansion of diagnoses and treatment to the point where there were none who dared resist and non who were not diagnosed. Being right when I wrote that Psychiatric diagnoses rested in marketing, not in science and that treating CFL (corporate financial lust) was fundamentally insane, but that the insanity did not lie with the patient.
And being right when I wrote that possible drugging would inevitably become mandated drugging, although neither the science or the treatments were any better.
Alas, like Cassandra, my predictions did not ring real when I wrote them but we have arrived where I saw us collectively headed. Dangerous drugs for everything that even smacks of real life and universal mandating just around the corner – if we turn that corner.
First, an admission: I am, by training, a Psychiatrist, encouraged by that training to treat children, adolescents and adults. But I was, I believe, saved from violating the basic ethical standard of medicine (and, with decency, every activity which involves any of us): Primum non nocere – Latin for “First Do No Harm”.
It is my considered belief, after considerable study, clinical practice and observation, that it is literally impossible to BE a practicing Psychiatrist, FOLLOWING THE PRACTICE GUIDELINES AND “STANDARD OF CARE IN THE COMMUNITY” PRACTICES, and NOT do harm, first, middle and last. That is why I have never treated anyone for anything using medication with two exceptions: a wildly psychotic 19 year old patient of mine in a State Hospital locked ward was suffering the torments of the damned (which is what he believed himself to be) as he unendingly hallucinated his inner terror. I prescribed for him enough sedation to allow him to stop screaming after 9 days of 24 hour nightmare. I was a First Year Resident at the time and knew nothing of orthomolecular psychiatry (the use of nutrients for mental relief and health), but I knew that I had to do something to help this young man by allowing him to reach into our world and us to reach into his. Once the madness-fear-madness cycle was broken, our work began. Ironically, my Chief Resident had just returned from a sojourn with the British Psychiatrist R. E. Liang, who saw schizophrenia as a glorious adventure so I had to go toe to toe with my superior and his superior and HIS superior to provide some respite for my young patient. I did and I won that battle.
Today, neither my Chief Resident, the well-known Dr. James Gordon, nor I would medicate that patient, both of us for very different reasons.
The other patient was a lady who had been addicted to Xanax(R) by her General Practitioner. I had to write a prescription for a small amount to complete weaning her from that intentionally highly addictive, and therefore highly profitable, psychoactive drug.
That takes care of my prescription history for psychiatric drugs over a 40 year career practicing medicine and psychiatry with some of the most seriously ill patients in the world. Successfully. Very Successfully.
So you can see that the article below chills me to the bone. It announces another step down the path of subservient lunacy for the disgraced profession of Psychiatry, a profession devoted to poisoning a specific target organ in the face of better, safer, cheaper, kinder and more effective options like nutrition and NeuroBioFeedback, appropriate therapies and social and health supports.
It is my considered view after 40 years of practice, that there is no place, that’s right, no place whatsoever, for psychiatric drugs. None. But, then, it is also my considered opinion that there is no place for any drugs in the Doctor’s office, although there is a place for them in the Emergency Room or ambulance while a patient is being transported there.
Psychiatrists no longer learn to talk to, and therefore, to listen to people. They are trained to look for flags that trigger this drug being prescribed or that one. The “literature” in their journals is mostly junk, paid for, authored by, and owned by the drug companies. But then, the “scientific journals” that publish them are, in reality, little more than advertising circulars for their magnificent, deceptive and callously dishonest advertisements. Just ask Marcia Angel, who resigned in protest as Editor of the [supposedly] prestigious New England Journal of Medicine because of the deep, dark and deadly corruption of the “peer review” system and the staggering lies upon which drug studies, and therefore prescription practices, rest.
In the Reuters article below you will see a future emerging in which there are no normals any more. Normal means having problems and problems are given names which suggest drug treatments. Suggest? Did I say suggest? Today, for most of us, most of the time, it is a suggestion. But it is a MUCH better business model if the suggestion is rhetorical and the requirement is absolute. More drugs sold. More side effects. More drugs added to the regimen. More side effects. More brain damage which looks exactly like the condition for which the drugs were given in the first place.
If this reminds you of the influenza shot for “protection” which turns out to be the CAUSE of the influenza “epidemic” each year which then leads to more calls for more vaccines “against” the influenza “epidemic” and drugs to “treat” what was induced by the shots: flu, cancer, autism, ALS, infertility, diabetes, etc., etc., etc., then you are paying attention. The business model is identical.
And just as the flu shot is transitioning from voluntary to mandatory, so the use of psychoactive drugs, all of them, for “diseases” and “conditions” that any decent human being would be ashamed to label another person with, let alone “treat” them for, will soon be mandatory unless we collectively say “NO!”, as we did to the Swine Flu vaccination (now included in this year’s dangerous seasonal flu shot.
Here’s you bit: Help support the Stop the Shot lawsuit against the FDA. Now that H1N1 vaccine will be added to the seasonal flu shot, the women who lost their babies after they took it are especially important plaintiffs in this case. Click here, http://www.healthfreedomusa.org/?page_id=189, to set up your recurring tax deductible donation, large or small. Act now, before the Diagnostic and Statistical Manual declares caring about your life and your body a mental disorder, as caring about a healthy diet and clean food has become. There are, by the way, two names for this “disorder”:
1. “Orthorexia| from “Ortho” meaning correct and “orexis” meaning appetite
2. Complete, total and unmitigated garbage.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
(Reuters) – An updated edition of a mental health bible for doctors may include diagnoses for “disorders” such as toddler tantrums and binge eating, experts say, and could mean that soon no-one will be classed as normal.
Leading mental health experts gave a briefing on Tuesday to warn that a new edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM), which is being revised now for publication in 2013, could devalue the seriousness of mental illness and label almost everyone as having some kind of disorder.
Citing examples of new additions like “mild anxiety depression,” “psychosis risk syndrome,” and “temper dysregulation disorder,” they said many people previously seen as perfectly healthy could in future be told they are ill.
“It’s leaking into normality. It is shrinking the pool of what is normal to a puddle,” said Til Wykes of the Institute of Psychiatry at Kings College London.
The DSM is published by the American Psychiatric Association (APA) and contains descriptions, symptoms, and other criteria for diagnosing mental disorders. It is seen as the global diagnostic bible for the field of mental health medicine.
The criteria are designed to provide clear definitions for professionals who treat patients with mental disorders, and for researchers and pharmaceutical drug companies seeking to develop new ways of treating them.
Wykes and colleagues Felicity Callard, also of Kings’ Institute of Psychiatry, and Nick Craddock of Cardiff University’s department of psychological medicine and neurology, said many in the psychiatric community are worried that the further the guidelines are expanded, the more likely it will become that nobody will be classed as normal any more.
“Technically, with the classification of so many new disorders, we will all have disorders,” they said in a joint statement. “This may lead to the belief that many more of us ‘need’ drugs to treat our ‘conditions’ — (and) many of these drugs will have unpleasant or dangerous side effects.”
The scientists said “psychosis risk syndrome” diagnosis was particularly worrying, since it could falsely label young people who may only have a small risk of developing an illness.
“It’s a bit like telling 10 people with a common cold that they are “at risk for pneumonia syndrome” when only one is likely to get the disorder,” Wykes told the briefing.
The American Psychiatric Association did not immediately respond to a request for comment.
The scientists gave examples from the previous revision to the DSM, which was called DSM 4 and included broader diagnoses and categories for attention deficit hyperactivity disorder (ADHD), autism and childhood bipolar disorders.
This, they said, had “contributed to three false epidemics” of these conditions, particularly in the United States.
“During the last decade, how many doctors were harangued by worried parents into giving drugs like Ritalin to children who didn’t really need it?,” their statement asked.
Millions of people across the world, many of them children, take ADHD drugs including Novartis’ Ritalin, which is known generically as methylphenidate, and similar drugs such as Shire Plc’s Adderall and Vyvanse. In the United States alone, sales of these drugs was about $4.8 billion in 2008.
Wykes and Callard published a comment in The Journal of Mental Health expressing their concern about the upcoming DSM revision and highlighting another 10 or more papers in the same journal from other scientists who were also worried. DSM 5 is due to be published in May 2013.
(Editing by Peter Graff)
http://www.reuters.com/article/idUSTRE66Q4BJ20100727
Dr. Laibow continues her commentary on the Codex Commission meeting, just concluded in Geneva, below.
Her other commentaries and brief-but-telling videos direct from the Commission meeting are at: http://www.healthfreedomusa.org/?p=5821. Don’t miss the important Action Items there as well!
We need your help to defray the costs of attending on your behalf.
RIDING THE FREEDOM MOUSE IS QUICK, EASY AND ESSENTIAL TO YOUR HEALTH FREEDOM!
Prevent S. 510 from being passed by the Senate. This Bill will industrialize and institutionalize our entire food supply — threatening natural (including organic), family, community and local gardens and farms — and cannot be allowed to take place. Click here, http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=4252, to take action once for each member of your family. Then, riding your Freedom Mouse, please forward this, and any other Action Items you feel are important enough to act upon, to everyone you can reach electronically with a short note reminding each of your contacts to do the same: take action once for every member of their families, and then forward to THEIR contact.
1. Stay in the Codex flow for you
2. Continue our critically important litigation to control the FDA and make it conform to US law (novel idea!)
3. Research and communicate to you what we find about health and health freedom: the good, the bad and the very, very ugly
4. Create Action Steps which impact policy
5. Maintain our network of action around the world
6. Help to reclaim the production of clean, unadulterated food world wide
7. All the other things that the Natural Solutions Foundation does for you and for health freedom, world-wide.
We know that the economy has been torpedoed and that money is tight. Does that make health freedom any less worthwhile! Please donate here: http://www.healthfreedomusa.org/?page_id=189.
AND NOW ON TO THE CODEX MEETING MACHINATIONS…
Codex has steadfastly refused to define consensus since by NOT having it defined, the Chair of a Codex session can declare just about anything that he/she wants to be approved as “approved by consensus”. Occasionally, of course, the delegates have come to a boiling point and raise such a ruckus that even the most audacious misuse of the concept of consensus fails. One such ruckus occurred the other day during the shameful attempt of this body, at the behest of the US, of course, to force the use of the dangerous and unnecessary drug Ractopamine™ on the food of an unwilling world. Another occurred, I am proud to say, when the Natural Solutions Foundation mobilized widespread opposition for the US-led attempt to put high levels of the metabolic poison fluoride in infant formula. More opposition of this coordinated sort is, of course a real danger to the globalists who seek to use Codex as their tool for control and depopulation.
Codex clearly realizes that the ability of the Natural Solutions Foundation to mobilize that sort of support and opposition is a significant reality and the abusive response of this corrupt and dangerous organization makes that quite clear.
Not able/willing to define “consensus” after 48 years of existence, the gentleman presenting at the front of the room has done it for this august body: he just announced, without any support from anyone, that WHO’s efforts on nutrition will not get universal agreement (a reasonable definition of consensus, I think you will agree) so WHO will not regard 75% agreement as “consensus”. That is rather staggering for an organization which presents itself as consensus-based, don’t you think? We do. And we think that it illustrates the corruption and disingenuousness of the deliberations, decisions and directions of this body.
We are, as I mentioned, sitting in the upper gallery of a nearly empty Codex meeting where we have been forced by aggressive guards.
General Stubblebine and I are so appalled at Codex’s continuing abuse of you, the food consuming stakeholders that we have written an Open Letter to the Codex Executive Committee which you can read here, http://www.healthfreedomusa.org/?p=5900. (Please come back after you read it!)
At the front of the empty room is a delegate talking about the establishment of a system for nutritional scientific guidance. He has extensive slides on the screen which document and expand what he is saying, which is, presumably, of enormous importance to the life and health of every consumer on the planet. General Stubblebine and I, here to represent and present YOUR interests, have been relegated to an upper gallery from which it is not possible to see the slides.
Nor is it possible to work under ordinary conditions of comfort and appropriate facilities although they exist in this room (but now where we are!):
You know that the US forbids the labeling of GMO “foods” while the EU has insisted on just such labeling. Well, no more. Yesterday, the European Parliament took an action which bring it closer to the food degradation of the US: From now on –
1. It will not longer be necessary to label GMO foods, including animals which have been fed GMO plants) as it has been previously and
2. Individual member states (formerly known as sovereign countries, you understand) will now be permitted to make their own decisions about whether to plant GMO crops and grow GMO animals.
Both of these actions are disastrous for health and well-being of the population, which is EXACTLY why they have been adopted, of course. GMO food and feed contaminates everything it touches. Since there are no meaningful boundaries or borders between one European country and another, the inevitable contamination and dominance of GMO crops is assured by this decision. Equally assured is the disastrous, but totally untraceable, health problems which await European eaters, useless or otherwise.
I received an immediate flurry of emails from European colleagues who understood how cataclysmically awful this was for their countries. I reminded each of them that under the coercive (and probably not legal) “Treaty of Lisbon” terms (which illegally adopted the European Union Constitution), a demand by 1 million EU citizens could force a reopening of the the issue being protested by these 1 million people.
Now 1 million is not bad and is eminently achievable. For that reason, the Natural Solutions Foundation will work with every European group which would like our organizational assistance. Please contact me at dr.laibow[at]gmail.com with “EU” as the subject line and the Trustees will do everything possible to support your redress of this vast error.
And if you want to help the “citizens” of the EU reclaim their food and health freedoms, join our forum at: http://groups.yahoo.com/group/NSF-EU
On a brighter note, the same day that traceability of GMO foods was wiped out, the same body rejected cloned meat, milk and other “foods” for human consumption in Europe. While we certainly do not endorse cloned food, it is odd that the known dangers of GMOs were accepted but the emotionally repugnant idea of cloned food. I cannot see any logic in accepting unlabeled poisons for humans while protecting them from replicated DNA. Logically, both should have been rejected roundly, soundly and permanently.
This brings us to the argument that the Natural Solutions Foundation is making that the US MUST be taken out of Codex. Although its structure may be crumbling and the cables that hold it up, so to speak, are fraying, Codex sets enormous amounts of food policy which is only allegedly “voluntary”. The US mis-uses every bit of its trade and scientific cachet here at Codex and makes huge strides, meeting by meeting, to use food for political gain and industry profit. Please visit http://www.healthfreedomusa.org/?p=5509, watch my video on getting the US out of Codex and then take our survey there to tell us if you agree or disagree.
Then, let’s get busy actually GETTING the US out of Codex — for the good of the whole world!
The malignant US impact on “food” around the world and of the US is enormous but, through their strong-arm “leadership” at Codex, it is all the more powerful. It is a primary reason I have called Codex “certifiably insane.” Although these actions were taken outside of Codex, the dirty hand of the US is all over this one. The Natural Solutions Foundation believes that, just as defeating the Fake Food Safety Bill, S. 510 will not stop the efforts of the Uber-Cartel to capture food, but it will weaken and disorganize it considerably, making it far easier to deal with, so getting the US out of Codex will do the same.
If ever there was an opportunity to deflect and defeat the globalists plans, it is now, centering around the control and contamination of food. We have a powerful opportunity for action here. Inaction, however, can kill huge numbers of us.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Just Exactly What Do Dr. Rima and Gen. Bert DO At Codex?
Find Out About Our Next Guest on the Dr. Rima Reports
Four Blog Links You MUST Click!
On the Road to Codex
Current ‘Must Take’ Action Items
Dr.Rima Recommends
Dr. Rima Live from Codex:
Wednesday, July 7 2:30 PM , Eastern with Kevin Trudeau at http://www.ktradionetwork.com/
Thursday, July 8, 10 AM Eastern with Fred van Liew at http://www.hthradio.com/
Don’t Forget to Order Your Valley of the Moon Coffee Now. Supplies Are LIMITED!
www.ValleyoftheMoonCoffee.org
What Does Attending a Codex Session Mean for Dr. Rima, Gen. Bert and YOU?
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.
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.
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:
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 importantly, 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 opposite 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.
And, as hard as it is, thanks for sending us to Codex. We still need your donations to finish defraying the cost (Geneva, Switzerland is a very expensive place!)
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
___________________________________________________________________
Listen to the Dr Rima Reports
Sunday Night Starting 9 PM Eastern to Midnight…
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 Nancy Orlen Weber, healer extraordinare! Nancy will talk with us about the exceptionally gentle and powerful
Raindrop® Technique and share her stories as a successful psychic detective.
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!
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
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!
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: www.DrRima.net 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
_________________________________________________
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!
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!
www.ValleyoftheMoonCoffee.org
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!
www.ValleyoftheMoonCoffee.org
_________________________________________
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” lista the three Dr. Rima Packs For more Details about the Packs:
http://www.healthfreedomusa.org/?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….
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 only 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!
In This Issue:
Find Out About Our Next Guest on the Dr. Rima Reports
Four Blog Links You MUST Click!
On the Road to Codex
Current ‘Must Take’ Action Items
Dr.Rima Recommends
GOOD NEWS! THE NATURAL SOLUTIONS NEW MARKETPLACE HAS RE-OPENED!
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 Nancy Orlen Weber, healer extraordinary! Nancy will talk with us about the exceptionally gentle and powerful
Raindrop® Technique and share her stories as a successful psychic detective.
Interested in aromatherapy? Visit http://www.drrima.net/#aroma
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@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!
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!
* Stop the Fake Food and Vitamin “Safety” Bill -S.510
* Oppose “Ear Candle” Ban!
* Health Keepers Oath
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!
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 products we love
_________________________________________________
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!
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!
www.ValleyoftheMoonCoffee.org
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!
www.ValleyoftheMoonCoffee.org
_________________________________________
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:
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….
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 only 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!
"I'm reading every news letter of yours for long time, signing every petition etc. and watching how we are loosing every freedom we had. I've got to do more. Thank you for everything you do."
