Archive for CODEX Consequences – Page 5
Natural Solutions Foundation
The Voice of Global Health AND FOOD Freedom™
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September 9, 2010
Permalink: http://drrimatruthreports.com/?p=6596
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This Week: Dr. Rima Interviews Charlotte Gerson and Howard Straus on The Long War Against Clean Food and Cancer Cures
September 19, 2010: Mike Adams, the Health Ranger, is our guest
September 26, 2010: John A. Crockett, Sr., a.k.a. Dr. “Mike Robe” on Soil Stewardship, Sanity and Survival
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IS THIS THE WEEK WE LET CLEAN FOOD DIE IN THE US? IT IS IF WE ALLOW S. 510 TO PASS
WE MUST TAKE ACTION AND THEN ACTIVATE YOUR ENTIRE NETWORK TO DO THE SAME
Congress is prepared to pass S. 510, the shockingly mis-named “Food Safety Bill”
Stop S. 510 NOW!
http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=4613
Take Action now to make sure that YOUR Senators place a “HOLD” on this bill to insure that it is not passed by “Unanimous Congressional Consent”. One Senator, placing, and sustaining, a hold on the bill can force it to be delayed, despite the demands of Monsanto and their friends. HOLD it until December and it dies with the close of this Congress.
This just in: we have word that a Senator from an important western State opposes the bill and may be willing to face down Big Agribiz. Take this Action Item IF there is support from other Senators.
It is urgent that you take action now even if you have raised your voice on this topic before because massed protesting voices are OUR SIDE’s lobbyist!
Ban GMOs NOW! Once-And-For-All Before There Is No Going Back
http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=2049
Listen to the Elderly: They Have Seen It All, And They’ll Tell It Exactly ‘Like It Is’. Especially Maxine
Let me get this straight.
We’re going to be “gifted” with a health care plan we are forced to purchase and fined if we don’t, written by a committee whose chairman says he doesn’t understand it, passed by a Congress that hasn’t read it but exempts themselves from it, to be signed by a president who also smokes, with funding administered by a treasury chief who didn’t pay his taxes, to be overseen by a surgeon general who is obese, and financed by a country that’s broke.
What the hell could possibly go wrong?
Well, Vaccines Could Be Mandated. That Would Make Something Go Wrong: Your Health, Your Freedom and Your Survival, For Example
Take These Action Items NOW and Then Pass Them On
Stop The Seasonal Flu/H1N1 Vaccine Madness
http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=4376
Support the Stop the Shot3 Vaccine Litigation
http://drrimatruthreports.com/?page_id=189
Stop the Slaughter: Demand Congress Investigate FDA’s Role in Autism and Other Vaccine Related Epidemics NOW!
http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=3688
Vaccines and vaccine mandates are very much in the wind, but not, alas, in the MMD, the Media of Mass Deception. Once the people of the US and most other countries of the world rejected, en mass, the absurd and dangerous H1N1 pandemic scam (including NY State and NJ both backing down on their vaccine mandates when the Natural Solutions Foundation and friends sued the State Health Departments in Federal Court), the Pholks at Big Pharma had some other tricks up their collective, and very dirty, sleeves. Recall as you read the rest of this article that there is not a single shred of evidence showing that ANY vaccine is either safe OR effective, let alone both, although such certainty is required by US law before any vaccine can be approved. Recall, too, that the US is the most vaccinated country in the world. And the sickest. And the most drugged. Recall that 1 American in 3 will die from cancer, a disease of under nutrition and environmental toxicity, including vaccine poisoning and chemicals in food (enter Codex!)
And recall that the US has:
1. Changed the ACIP (Advisory Committee on Immunization Practices, part of the CDC which is part of the Department of Health and Human Services, or HHS) Guidelines to recommend Seasonal Flu vaccination for everyone starting at 6 months and extending throughout the life span. What ACIP “recommends” generally becomes State, school and other agency mandates within a very short time.
“The 2010 ACIP guidelines emphasize the following:
* All persons at least 6 months old should receive annual vaccination for the 2010-2011 influenza season;
* During the 2010-2011 season, 2 doses of a 2010-2011 seasonal influenza vaccine should be given at a minimal interval of 4 weeks to children aged 6 months to 8 years with unknown vaccination status who have never received seasonal influenza vaccine before (or who received seasonal vaccine for the first time in 2009-2010 but received only 1 dose in their first year of vaccination), as well as to children who did not receive at least 1 dose of an influenza A (H1N1) 2009 monovalent vaccine regardless of previous influenza vaccine history…”
http://www.medscape.com/viewarticle/726213″
2. Included H1N1 vaccines in the “seasonal” flu shots for 2010-2011 flu season despite a total lack of medical requirement for such inclusion (or, indeed, for any vaccination, for that matter). People avoided the seasonal flu shots at the same time they avoided the H1N1 shots in 2009-2010 leading to the lightest flu season in memory. The correlation is excruciatingly clear: flu shots create disease. Disease is good business. Therefore we must have flu shots, says the global government.
3. Ignored totally the fact that Canada, Finland and Australia have taken the GSK flu vaccine off the market in those countries because of serious side effects. Side effects include an incurable neurological condition called “narcolepsy” or uncontrollable sleeping episodes, convulsions, miscarriages and death. Of course, the FDA holds that the tremendous increase in post vaccination miscarriages, among those side effects, is not worth worrying about.
4. Conveniently found a “professional organization” to call for mandatory vaccination of health care workers at peril of losing their jobs if they are unvaccinated. The Society for Healthcare Epidemiology of America, http://www.shea-online.org/, has done just that.
Healthcare professionals, however, are neither amused nor persuaded. In a Medscape Poll, the results are pretty much the same as they were last year when mandates were proposed for H1N1 vaccination of health care workers:
Among all responding HealthCare Professionals, 28% strongly favored the mandatory vaccination while 58% strongly opposed it.
Among physicians, a generally strongly pro-vaccination group, the results are extremely interesting:
36% strongly agree with the mandates while 44% strongly oppose them.
For nurses, who tend to be closer to the adverse events associated with vaccination, those strongly agreeing with the need for a mandate, 26%, were strongly outnumbered by those opposing it, 59%.
Only 34% of pharmacists, who sell the vaccines, strongly endorsed the mandate while 46% strongly opposed it.
Not one group of polled health professionals in the US endorsed a mandate. Here, by the way, is the question which these health professionals were asked in this survey:
“The Society for Healthcare Epidemiology of America (SHEA) recently released a policy paper recommending that healthcare workers be required to get the seasonal flu vaccine or face losing their job and professional privileges. Do you favor or oppose SHEA’s recommendation on mandatory vaccination for healthcare workers?”
http://www.medscape.com/px/instantpollservlet/result?PollID=3356&src=mp&spon=17&uac=117629CN
But Wait! There’s More [Vaccination]
The US Government, including FDA, CDC and ACIP cannot, apparently, get enough vaccines into the public. The Department of Defense (DOD) is not far behind since civilians working for the DoD Schools in Europe were notified on July 30, 2010 that their Swine Flu AND Seasonal vaccination was mandatory and that failure to receive this vaccination would result in dismissal from their jobs. Likewise, about 30,000 students are now required to receive the untested and unnecessary vaccines despite the fact that WHO has publicly rescinded their failed “Level 6 Pandemic” attempt.
Stars and Striped, a DoD publication, said,
“The immunization policy, mandated by U.S. European Command [EUCOM], covers both the seasonal and swine flu viruses and applies to teachers and employees at more than 80 Department of Defense Dependents Schools [DoDDS] in Europe, as well as 30,000 students. Children older than 6 months enrolled in base daycare centers and daycare center workers throughout Europe also are affected by the move.
“We fully support the EUCOM policy,” said DODDS-Europe spokeswoman Margaret Menzie”
http://www.stripes.com/news/flu-shots-mandatory-for-students-teachers-at-dodds-europe-schools-1.112858
So we Health Freedom advocates have to ask “Who owns the body of these teachers and their students?” Apparently, the Department of Defense does. And just who owns your body?
In October, 2009, GSK’s HPV vaccine, Cervavax, the first vaccine in the US to contain an oil in water adjuvant (similar to the dangerous compound squalene), was recommended for use in girls 10-25 years of age. Merck’s Gardasil is already approved for use for girls between 11 and 26. http://www.medscape.com/viewarticle/722855?src=mp&spon=34&uac=117629CN
Medical Insanity Alert – Fasten Your Intellectual Seat Belt!
Now, take a deep breath and look at these two headlines from today’s issue of Medscape Daily News, an electronic medical science newsletter which I receive each day:
Guidelines Updated for Use of 23-Valent Pneumococcal Polysaccharide Vaccine in Adults [A 23-valent vaccine is supposedly effective against 23 different types of disease causing organisms, in this case, bacteria – Dr. Rima]
September 8, 2010 “Invasive disease from Streptococcus pneumoniae (pneumococcus) is a major cause of illness and death in the United States, with an estimated 43,500 cases and 5,000 deaths among persons of all ages in 2009,” write J. P. Nuorti, MD, DSc, and C. G. Whitney, MD, from the Division of Bacterial Diseases, National Center for Immunization and Respiratory Diseases, US Centers for Disease Control and Prevention, for the Advisory Committee on Immunization Practices (ACIP) Pneumococcal Vaccines Working Group. “This report provides updated recommendations from the …ACIP for prevention of invasive pneumococcal disease (IPD) (i.e., bacteremia, meningitis, or infection of other normally sterile sites through use of the …PPSV23 among all adults aged ?65 years and those adults aged 19-64 years with underlying medical conditions that put them at greater risk for serious pneumococcal infection.”
Pneumococcal Vaccine Dosing Schedule Linked to Higher Risk of Acquiring Multiresistant Strain [This vaccine is only /supposedly/ effective against 7 types of disease causing bacteria – Dr. Rima]
September 7, 2010 “A 2 + 1 pneumococcal vaccine dosing schedule is linked to an increased risk of acquiring a multiresistant strain, according to the results of a study reported in the September 8 issue of the Journal of the American Medical Association.
“The rapid increase in multiresistant serotype 19A as a cause of invasive and respiratory pneumococcal disease has been associated in time with the widespread implementation of 7-valent pneumococcal conjugate vaccination (PCV-7) in several countries,” write Elske J. M. van Gils, MD, from University Medical Center Utrecht in Utrecht, the Netherlands, and colleagues.”
What could be crazier? The vaccine we have approved causes resistant organisms to develop and leaves people more susceptible to infection with them. YES! NOW, let’s create not a 7 organism vaccine, but a 23 organism one and watch this one screw up people’s immune systems so that not even the most potent antibiotic will work.
Nano silver? Oh, let’s ban it the way we have in Europe since it IS the universal safe, effective and inexpensive antibiotic which makes all other antibiotics unnecessary. Gives the lie to vaccines, too, since with a good immune system and nano silver you loose even the pretext that they have any place in health or prevention.
We recommend www.Nutronix.com/naturalsolutions as a source of our favorite nano-silver.
And then there’s this:
Flu Shot No Better than Placebo in Preventing Asthma Attacks
Stockholm, Sweden, September 16, 2002.
A new Swedish study has found that flu vaccine is “possibly no better than placebo in preventing exacerbations in asthmatic children.” Reporter Cameron Johnston reports that “Asthmatic children and other groups are usually encouraged to receive the flu vaccine each year as winter approaches. However, according to one study, the flu vaccine may be no better than placebo for preventing influenza-induced asthma exacerbation among children.
and this:
Japan Abandons flu Shots for Children
Large scale studies of compulsory flu vaccination in Japan of school aged children showed the vaccine to be ineffective and conducive to lawsuits due to adverse side effects. Two large studies one in 1980 and the other in 1985, involving four cities with vaccination rates between 1% and 90% showed little difference in flu incidence. In 1987, the Japanese government changed the flu vaccine from compulsory to voluntary. By 1989, even though only 20% of the population took the flu vaccine, the incidence of influenza did not increase. http://www.whale.to/vaccines/flu7.html
and this:
“One of the most bizarre twists on the flu vaccine saga is the CDC recommendation of 2001 that all pregnant women receive the vaccine in their second or third trimester. This recommendation even has doctors confused, since the vaccine remains a category C drug (unknown risk for pregnancy). No adequate studies have been conducted to monitor safety of the vaccine for mother and fetus. The only studies of adverse effects in pregnancy were conducted in the 1970s (Heinonen et al., 1973; Sumaya & Gibbs, 1979). Some flu vaccines still contain mercury as a preservative, despite a 1998 FDA instruction to remove mercury from all drugs. According to the CDC, two groups are most vulnerable to methylmercury, the fetus and children ages 14 and younger. An article published in the American Journal of Epidemiology in 1999 stated, “the greatest susceptibility to methylmercury neurotoxicity occurs during late gestation” (Grandjean et al., 1999). How did CDC committee members determine that flu vaccines were safe for pregnant women? They did not. The committee, despite its own recommendation, states, “additional data are needed to confirm the safety of vaccination during pregnancy” (CDC, 2001b).
http://vran.org/about-vaccines/specific-vaccines/influenza-vaccine-flu-shot/resisting-the-flu-vaccine-hype-for-children/
and this:
Dr. Hugh Fudenberg, one of the world’s leading immunogeneticists, states the chances of getting Alzheimer’s disease is 10 times higher if an individual has five consecutive shots than if they have one, two or no shots.
Source: transcribed notes of Dr. Fudenberg’s speech at the NVIC International Vaccine Conference, Arlington, VA September, 1997
and on and on and on and on. Yet the government insists vaccines are safe and effective just as if there were a shred of real evidence that they are either one.
This is simple madness. The craziness that is vaccination MUST stop at your body and your children’s. The choice is yours.
The One With the Best Songs Wins
And Pharma Doesn’t Sing!
Dr. Rima’s Pig In A Poke – Radical Rap
http://www.youtube.com/watch?v=xVGrudg6mQ8
Roger Mason’s Prize Winning Music Video Setting of Dr. Rima’s Uber Cartel March
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Michael Belkin and the Refusers
“Get Your Mandate Out of My Body!”
http://www.reverbnation.com/play_now/song_4193997
Alan G. Phillips, JD’s “Shine Your Light”
http://pandemicresponseproject.com/ShareYourLight.html
Mike Adams’ “Vaccine Zombie”
http://www.youtube.com/watch?v=qYI-dC9G0us
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Action Item: Tell the Senate: “NO!” – http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=4613
Dr. Laibow: Stop S.510 Now!
S. 510, the fake “Food Safety” Bill, 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 1279 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.
We lost the clean food battle in the House.
The battle ground then shifted to the Senate. Remember, the Uber Cartel, which includes Big Agra, Big Chema, Big Biotech and, behind them all, Big Pharma and its malignant sister, Big Oil, has endless money for lobbyists, propaganda, back-door dealings and other well-financed pressure tactics like Codex Alimentarius, for example.
For examples of corruption, we have only to look at the current Congressional probe of the Uber Cartel Pharma Phamily corruption, bribing and buying their way into national policy around the world through filling personal coffers of regulators and politicians. If you think that is limited to foreign countries, guess again.
So the fact that we, the Natural Solutions Foundation net roots and those who have joined us in this clean food battle, following our lead and bringing their constituencies into the fray, have held off the passage of the bill that some have called “Monsanto’s wet dream Bill” since last November, when unanimous Senate agreement on its passage was reached is nothing short of miraculous.
Miraculous and, if we falter now, totally meaningless.
Once we pushed it back in November, the Uber Cartel was unable to move it forward: there were too many of us who got the picture, understood the game and comprehended what the cost would be to our health and our freedom if we did not succeed in killing this bill before it, literally, killed us.
Now we are met on the battle field of clean food again. In mid April S 510 was once again the subject of unanimous agreement and was to be voted upon the following week. Our inside sources shared that information with us and we rose up in our collective power, sending so many emails to Congress, and activating so many Washington forces that the bill went into limbo again.
Later, as the Senate was winding up its session before summer recess, we realized that the plan was to ram it through as a “noncontroversial” bill, which would then be passed by “unanimous Congressional Consent” since no one had anything to say about it.
Well, we used the Senate rules against this bill and asked you to demand of your Senators that they put a hold on S. 510 by calling the Senate Cloak Room (yes, you read that right!) and demanding that the bill not go up for a unanimous consent approval.
Again, we prevailed and the US Senate broke for its 2010 summer recess without voting on the bill.
Enter villains gnashing teeth and twirling mustaches.
S. 510, the fake “Food Safety Bill”, is of enormous importance to the globalist genocidalists. They want it passed. Senators who are either their dupes or their bed mates are willing to do their bidding IF, and only IF, they can do so out of the light of public awareness. They want to do their masters’ bidding without being tarred with the same brush of filth as their masters.
We, you and I, are here to make sure that they are publicly exposed and publicly notified by vast numbers of us that their doings are very, very public and that their constituents, you and I, are holding them personally, and professionally, accountable for their actions.
It is urgently important that the eaters of the US join together, whether we are male or females, young or old, single or married, Christian or Jew or Jain or Muslim or atheist or Hindu, parents or childless persons, unite behind this issue.
Click the NEW Action Item here, http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=4613, whether you have taken action on this item or not. Then I urge you to become the flaming sword of dissemination and freedom through your email work. There is no one who does not eat. There is no one who is not impacted by the quality of the food that they eat. There is no one who, no matter what the choices that they actually make might be, does not want the RIGHT to choose clean, unadulterated food if they want to.
What’s at stake?
1. No seed saving without vast expenditures because seeds could be a terrorist weapon! What’s really going on here? Biotech companies want to control the world’s food access and sell ONLY their own chemical dependent seeds.
2. All seed prices, already consuming more than 1/3 of all farmers’ expenditures, will be controlled by the Uber Cartel.
3. Organic, clean, local, personal farming would still be allowed IF Codex standards and guidelines were followed. These include irradiation, chemical use and other highly dangerous, expensive and unacceptable practices for clean food consumers (those of us recently identified by the captive organization called the American Psychiatric Association as suffering from “Orthorexia”, as psychiatric disorder in which people are concerned with the quality of the food they eat!).
4. Growing personal or local food without the taxes and controls inherent in this bill will become criminal acts.
5. Record keeping will be so burdensome, and the fines for not complying, that most small, family, organic and biodynamic farmers will cease to produce food for themselves or you.
6. Supplements (attacked by Senator McCain in a bill which was ‘absorbed’ into S. 510) will be attacked even more strongly than they currently are since, as foods, they, too, will have to meet the “standards” imposed by S. 510 despite the fact that they are among the most highly regulated foods in the country AND the safest.
7. Health will decline as more chemicals are used by farms, more toxic effluent enters the environment, less nutritious food is available, more chemical contamination is permitted, even more food is irradiated and high potency supplements disappear. The diseases of under nutrition, including cancer, cardiovascular disease, stroke, diabetes and obesity, already epidemic, will sky rocket, along with the endless human suffering which accompany them.
8. Raw milk will be a thing of the past.
9. Freedom, like raw milk, will be a memory of what we used to be able to access.
In case you haven’t heard already, Speaker Pelosi called my colleagues and me back from the August recess on Tuesday to vote on more government spending. This one comes in the form of a bailout package to help states cover the costs for education and Medicaid to the tune of $26 billion. And here I thought the American public would finally get some reprieve from the voracious spending appetite of liberal Democrats in Washington, DC.
It should come as no surprise for you to know that I voted against this bill. Not only does it spend money that we don’t have, but it perpetuates the bailout culture that has become so popular with Democrats in Congress. Also, but the so-called spending “offsets” in the bill came in the form of a $10 billion tax increase on corporations.
Democrats would like you to believe that spending this additional $26 billion will somehow create jobs, spur economic growth and expand individual opportunity for Americans. The truth is that this latest bailout is really just a give-away to state bureaucrats at the expense of U.S. taxpayers. Another short-term federal bailout will only encourage states to rely on more taxpayer funded federal assistance rather than balancing their budgets and reducing unneeded spending.
Now is the time to act. Tomorrow may well be too late.
Single voices are good. Multipliers of many thousands makes our voices count – powerfully.
And… voices backed by resources are the most powerful of all!
Please donate; every dollar helps protect health and food freedom:
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Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.DrRima.net
www.HealthFreedomUSA.org
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Natural Solutions Foundation
The Voice of Global Health Freedom(TM)
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Permalink: http://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
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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 Voice of Global Health Freedom™
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Permalink: http://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
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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
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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.
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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