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Doctors Warn: Avoid Genetically Modified Food

By Jeffrey M. Smith

On May 19th, the American Academy of Environmental Medicine (AAEM) called on Physicians to educate their patients, the medical community, and the public to avoid GM (genetically modified) foods when possible and provide educational materials concerning GM foods and health risks.[1] They called for a moratorium on GM foods, long-term independent studies, and labeling. AAEM’s position paper stated, Several animal studies indicate serious health risks associated with GM food, including infertility, immune problems, accelerated aging, insulin regulation, and changes in major organs and the gastrointestinal system. They conclude, There is more than a casual association between GM foods and adverse health effects. There is causation, as defined by recognized scientific criteria. The strength of association and consistency between GM foods and disease is confirmed in several animal studies.

More and more doctors are already prescribing GM-free diets. Dr. Amy Dean, a Michigan internal medicine specialist, and board member of AAEM says, I strongly recommend patients eat strictly non-genetically modified foods. Ohio allergist Dr. John Boyles says I used to test for soy allergies all the time, but now that soy is genetically engineered, it is so dangerous that I tell people never to eat it.

Dr. Jennifer Armstrong, President of AAEM, says, Physicians are probably seeing the effects in their patients, but need to know how to ask the right questions. World renowned biologist Pushpa M. Bhargava goes one step further. After reviewing more than 600 scientific journals, he concludes that genetically modified organisms (GMOs) are a major contributor to the sharply deteriorating health of Americans.

Pregnant women and babies at great risk

Among the population, biologist David Schubert of the Salk Institute warns that children are the most likely to be adversely effected by toxins and other dietary problems related to GM foods. He says without adequate studies, the children become the experimental animals.[2]

The experience of actual GM-fed experimental animals is scary. When GM soy was fed to female rats, most of their babies died within three weeks compared to a 10% death rate among the control group fed natural soy.[3] The GM-fed babies were also smaller, and later had problems getting pregnant.[4]

When male rats were fed GM soy, their testicles actually changed color from the normal pink to dark blue.[5] Mice fed GM soy had altered young sperm.[6] Even the embryos of GM fed parent mice had significant changes in their DNA.[7] Mice fed GM corn in an Austrian government study had fewer babies, which were also smaller than normal.[8]

Reproductive problems also plague livestock. Investigations in the state of Haryana, India revealed that most buffalo that ate GM cottonseed had complications such as premature deliveries, abortions, infertility, and prolapsed uteruses. Many calves died. In the US, about two dozen farmers reported thousands of pigs became sterile after consuming certain GM corn varieties. Some had false pregnancies; others gave birth to bags of water. Cows and bulls also became infertile when fed the same corn.[9]

In the US population, the incidence of low birth weight babies, infertility, and infant mortality are all escalating.

Food designed to produce toxin

GM corn and cotton are engineered to produce their own built-in pesticide in every cell. When bugs bite the plant, the poison splits open their stomach and kills them. Biotech companies claim that the pesticide, called Bt produced from soil bacteria Bacillus thuringiensis has a history of safe use, since organic farmers and others use Bt bacteria spray for natural insect control. Genetic engineers insert Bt genes into corn and cotton, so the plants do the killing.

The Bt-toxin produced in GM plants, however, is thousands of times more concentrated than natural Bt spray, is designed to be more toxic,[10] has properties of an allergen, and unlike the spray, cannot be washed off the plant.

Moreover, studies confirm that even the less toxic natural bacterial spray is harmful. When dispersed by plane to kill gypsy moths in the Pacific Northwest, about 500 people reported allergy or flu-like symptoms. Some had to go to the emergency room.[11],[12]

The exact same symptoms are now being reported by farm workers throughout India, from handling Bt cotton.[13] In 2008, based on medical records, the Sunday India reported, Victims of itching have increased massively this year . . . related to BT cotton farming.[14]

GMOs provoke immune reactions

AAEM states, Multiple animal studies show significant immune dysregulation, including increase in cytokines, which are associated with asthma, allergy, and inflammation all on the rise in the US.

According to GM food safety expert Dr. Arpad Pusztai, changes in the immune status of GM animals are a consistent feature of all the studies.[15] Even Monsanto’s own research showed significant immune system changes in rats fed Bt corn.[16] A November 2008 by the Italian government also found that mice have an immune reaction to Bt corn.[17]

GM soy and corn each contain two new proteins with allergenic properties,[18] GM soy has up to seven times more trypsin inhibitor a known soy allergen,[19] and skin prick tests show some people react to GM, but not to non-GM soy.[20] Soon after GM soy was introduced to the UK, soy allergies skyrocketed by 50%. Perhaps the US epidemic of food allergies and asthma is a casualty of genetic manipulation.

Animals dying in large numbers

In India, animals graze on cotton plants after harvest. But when shepherds let sheep graze on Bt cotton plants, thousands died. Post mortems showed severe irritation and black patches in both intestines and liver (as well as enlarged bile ducts). Investigators said preliminary evidence strongly suggests that the sheep mortality was due to a toxin. . . . most probably Bt-toxin.[21] In a small follow-up feeding study by the Deccan Development Society, all sheep fed Bt cotton plants died within 30 days; those that grazed on natural cotton plants remained healthy.

In a small village in Andhra Pradesh, buffalo grazed on cotton plants for eight years without incident. On January 3rd, 2008, the buffalo grazed on Bt cotton plants for the first time. All 13 were sick the next day; all died within 3 days.[22]

Bt corn was also implicated in the deaths of cows in Germany, and horses, water buffaloes, and chickens in The Philippines.[23]

In lab studies, twice the number of chickens fed Liberty Link corn died; 7 of 20 rats fed a GM tomato developed bleeding stomachs; another 7 of 40 died within two weeks.[24] Monsanto’s own study showed evidence of poisoning in major organs of rats fed Bt corn, according to top French toxicologist G. E. Seralini.[25]

Worst finding of all GMOs remain inside of us

The only published human feeding study revealed what may be the most dangerous problem from GM foods. The gene inserted into GM soy transfers into the DNA of bacteria living inside our intestines and continues to function.[26] This means that long after we stop eating GMOs, we may still have potentially harmful GM proteins produced continuously inside of us. Put more plainly, eating a corn chip produced from Bt corn might transform our intestinal bacteria into living pesticide factories, possibly for the rest of our lives.

When evidence of gene transfer is reported at medical conferences around the US, doctors often respond by citing the huge increase of gastrointestinal problems among their patients over the last decade. GM foods might be colonizing the gut flora of North Americans.

Warnings by government scientists ignored and denied

Scientists at the Food and Drug Administration (FDA) had warned about all these problems even in the early 1990s. According to documents released from a lawsuit, the scientific consensus at the agency was that GM foods were inherently dangerous, and might create hard-to-detect allergies, poisons, gene transfer to gut bacteria, new diseases, and nutritional problems. They urged their superiors to require rigorous long-term tests.[27] But the White House had ordered the agency to promote biotechnology and the FDA responded by recruiting Michael Taylor, Monsanto’s former attorney, to head up the formation of GMO policy. That policy, which is in effect today, denies knowledge of scientists’ concerns and declares that no safety studies on GMOs are required. It is up to Monsanto and the other biotech companies to determine if their foods are safe. Mr. Taylor later became Monsanto’s vice president.

Dangerously few studies, untraceable diseases

AAEM states, GM foods have not been properly tested and pose a serious health risk. Not a single human clinical trial on GMOs has been published. A 2007 review of published scientific literature on the potential toxic effects/health risks of GM plants revealed that experimental data are very scarce. The author concludes his review by asking, Where is the scientific evidence showing that GM plants/food are toxicologically safe, as assumed by the biotechnology companies?[28]

Famed Canadian geneticist David Suzuki answers, The experiments simply haven’t been done and we now have become the guinea pigs. He adds, Anyone that says, ‘Oh, we know that this is perfectly safe,’ I say is either unbelievably stupid or deliberately lying.[29]

Dr. Schubert points out, If there are problems, we will probably never know because the cause will not be traceable and many diseases take a very long time to develop. If GMOs happen to cause immediate and acute symptoms with a unique signature, perhaps then we might have a chance to trace the cause.

This is precisely what happened during a US epidemic in the late 1980s. The disease was fast acting, deadly, and caused a unique measurable change in the blood but it still took more than four years to identify that an epidemic was even occurring. By then it had killed about 100 Americans and caused 5,000-10,000 people to fall sick or become permanently disabled. It was caused by a genetically engineered brand of a food supplement called L-tryptophan.

If other GM foods are contributing to the rise of autism, obesity, diabetes, asthma, cancer, heart disease, allergies, reproductive problems, or any other common health problem now plaguing Americans, we may never know. In fact, since animals fed GMOs had such a wide variety of problems, susceptible people may react to GM food with multiple symptoms. It is therefore telling that in the first nine years after the large scale introduction of GM crops in 1996, the incidence of people with three or more chronic diseases nearly doubled, from 7% to 13%.[30]

To help identify if GMOs are causing harm, the AAEM asks their members, the medical community, and the independent scientific community to gather case studies potentially related to GM food consumption and health effects, begin epidemiological research to investigate the role of GM foods on human health, and conduct safe methods of determining the effect of GM foods on human health.

Citizens need not wait for the results before taking the doctors advice to avoid GM foods. People can stay away from anything with soy or corn derivatives, cottonseed and canola oil, and sugar from GM sugar beets unless it says organic or non-GMO. There is a pocket Non-GMO Shopping Guide, co-produced by the Institute for Responsible Technology and the Center for Food Safety, which is available as a download, as well as in natural food stores and in many doctors’ offices.

If even a small percentage of people choose non-GMO brands, the food industry will likely respond as they did in Europe by removing all GM ingredients. Thus, AAEM’s non-GMO prescription may be a watershed for the US food supply.

SOURCE:

[1] http://www.aaemonline.org/gmopost.html

[2] David Schubert, personal communication to H. Penfound, Greenpeace Canada, October 25, 2002.

[3] Irina Ermakova, Genetically modified soy leads to the decrease of weight and high mortality of rat pups of the first generation. Preliminary studies, Ecosinform 1 (2006): 4-9.

[4] Irina Ermakova, Experimental Evidence of GMO Hazards, Presentation at Scientists for a GM Free Europe, EU Parliament, Brussels, June 12, 2007 [5] Irina Ermakova, Experimental Evidence of GMO Hazards, Presentation at Scientists for a GM Free Europe, EU Parliament, Brussels, June 12, 2007

[6] L. Vecchio et al, Ultrastructural Analysis of Testes from Mice Fed on Genetically Modified Soybean, European Journal of Histochemistry 48, no. 4 (Oct-Dec 2004):449-454.

[7] Oliveri et al., Temporary Depression of Transcription in Mouse Pre-implantion Embryos from Mice Fed on Genetically Modified Soybean, 48th Symposium of the Society for Histochemistry, Lake Maggiore (Italy), September 7-10, 2006.

[8] Alberta Velimirov and Claudia Binter, Biological effects of transgenic maize NK603xMON810 fed in long term reproduction studies in mice, Forschungsberichte der Sektion IV, Band 3/2008

[9] Jerry Rosman, personal communication, 2006

[10] See for example, A. Dutton, H. Klein, J. Romeis, and F. Bigler, Uptake of Bt-toxin by herbivores feeding on transgenic maize and consequences for the predator Chrysoperia carnea, Ecological Entomology 27 (2002): 441-7; and J. Romeis, A. Dutton, and F. Bigler, Bacillus thuringiensis toxin (Cry1Ab) has no direct effect on larvae of the green lacewing Chrysoperla carnea (Stephens) (Neuroptera: Chrysopidae), Journal of Insect Physiology 50, no. 2-3 (2004): 175-183.

[11] Washington State Department of Health, Report of health surveillance activities: Asian gypsy moth control program, (Olympia, WA: Washington State Dept. of Health, 1993).

[12] M. Green, et al., Public health implications of the microbial pesticide Bacillus thuringiensis: An epidemiological study, Oregon, 1985-86, Amer. J. Public Health 80, no. 7(1990): 848-852.

[13] Ashish Gupta et. al., Impact of Bt Cotton on Farmers’ Health (in Barwani and Dhar District of Madhya Pradesh), Investigation Report, Oct-Dec 2005.

[14] Sunday India, October, 26, 2008

[15] October 24, 2005 correspondence between Arpad Pusztai and Brian John

16] John M. Burns, 13-Week Dietary Subchronic Comparison Study with MON 863 Corn in Rats Preceded by a 1-Week Baseline Food Consumption Determination with PMI Certified Rodent Diet #5002, December 17, 2002http://www.monsanto.com/monsanto/content/sci_tech/prod_safety/fullratstudy.pdf

[17] Alberto Finamore, et al, Intestinal and Peripheral Immune Response to MON810 Maize Ingestion in Weaning and Old Mice, J. Agric. Food Chem., 2008, 56 (23), pp 11533-11539, November 14, 2008

[18] See L Zolla, et al, Proteomics as a complementary tool for identifying unintended side effects occurring in transgenic maize seeds as a result of genetic modifications, J Proteome Res. 2008 May;7(5):1850-61; Hye-Yung Yum, Soo-Young Lee, Kyung-Eun Lee, Myung-Hyun Sohn, Kyu-Earn Kim, Genetically Modified and Wild Soybeans: An immunologic comparison, Allergy and Asthma Proceedings 26, no. 3 (May-June 2005): 210-216(7); and Gendel, The use of amino acid sequence alignments to assess potential allergenicity of proteins used in genetically modified foods, Advances in Food and Nutrition Research 42 (1998), 45-62.

[19] A. Pusztai and S. Bardocz, GMO in animal nutrition: potential benefits and risks, Chapter 17, Biology of Nutrition in Growing Animals, R. Mosenthin, J. Zentek and T. Zebrowska (Eds.) Elsevier, October 2005

[20] Hye-Yung Yum, Soo-Young Lee, Kyung-Eun Lee, Myung-Hyun Sohn, Kyu-Earn Kim, Genetically Modified and Wild Soybeans: An immunologic comparison, Allergy and Asthma Proceedings 26, no. 3 (May-June 2005): 210-216(7).

[21] Mortality in Sheep Flocks after Grazing on Bt Cotton Fields Warangal District, Andhra Pradesh Report of the Preliminary Assessment, April 2006, http://www.gmwatch.org/archive2.asp

[22] Personal communication and visit, January 2009.

[23] Jeffrey M. Smith, Genetic Roulette: The Documented Health Risks of Genetically Engineered Foods, Yes! Books, Fairfield, IA USA 2007

[24] Arpad Pusztai, Can Science Give Us the Tools for Recognizing Possible Health Risks for GM Food? Nutrition and Health 16 (2002): 73-84.

[25] Stephane Foucart, Controversy Surrounds a GMO, Le Monde, 14 December 2004; referencing, John M. Burns, 13-Week Dietary Subchronic Comparison Study with MON 863 Corn in Rats Preceded by a 1-Week Baseline Food Consumption Determination with PMI Certified Rodent Diet #5002, December 17, 2002 http://www.monsanto.com/monsanto/content/sci_tech/prod_safety/fullratstudy.pdf

[26] Netherwood et al, Assessing the survival of transgenic plant DNA in the human gastrointestinal tract, Nature Biotechnology 22 (2004): 2.

[27] See memos at www.biointegrity.org

[28] José Domingo, Toxicity Studies of Genetically Modified Plants : A Review of the Published Literature, Critical reviews in food science and nutrition, 2007, vol. 47, no8, pp. 721-733

[29] Angela Hall, Suzuki warns against hastily accepting GMOs, The Leader-Post (Canada), 26 April 2005.

[30] Kathryn Anne Paez, et al, Rising Out-Of-Pocket Spending For Chronic Conditions: A Ten-Year Trend, Health Affairs, 28, no. 1 (2009): 15-

If prescription drugs are so good, where are all the healthy drug takers?

by Mike Adams, the Health Ranger

When observing the state of modern medicine and the unprecedented influence of pharmaceuticals, an interesting paradox arises. The drug companies claim that pharmaceuticals can do wonders for people: lower their cholesterol, end clinical depression, reverse osteoporosis, eliminate allergies, calm your children and many other similar promises. But if prescription drugs are so good for people, where are all the healthy medicated customers?

There aren’t any to speak of. There’s nobody taking twelve prescriptions who has a clean bill of health. In fact, the more prescriptions a person takes, the worse their overall health. And if you approach the healthiest people you can find in a local fitness center and ask what prescription drugs they’re taking in order to be so healthy, they’ll give you a rather confused look: they don’t take prescription drugs!.

So how is it that the pharmaceutical industry can be claiming to make people healthier in the first place? And what happened to common sense here? A rigorous scientific view of the whole situation can only conclude that prescription drugs are, in fact, making people sicker. It’s like a massive clinical trial, and the results of the trial are rather obvious: we’re swallowing more drugs than ever, and we’re getting sicker. In fact, the more drugs a person takes, and the longer they take them, the more rapidly their overall health deteriorates.

So why are drugs approved in the first place?

During development, prescription drugs are designed to target a single measurable marker, such as cholesterol levels or bone density. There are thousands of such markers to target in the world of modern medicine, and if a specific drug can alter any measurable marker in a positive direction — without killing too many people during the clinical trials– the FDA eventually declares it to be “safe and effective” and the drug is unleashed for public consumption.

Indeed, the drug may effectively impact that one marker. But here’s where the problem starts: every drug has a systemic effect, and these systemic effects are not accurately measured (or admitted) in clinical trials. For example, statin drugs do, in fact, lower bad cholesterol levels. But they do this by compromising the ability of the liver to create all types of cholesterol, including the “good” cholesterol and important hormones that the body manufactures from cholesterol. Statins may have one measurable, positive effect according to the medical charts, but they simultaneously throw off the body’s healthy physiology in a hundred other ways such as blocking your sex drive.

Clinical trials don’t pay much attention to these other effects; they’re just looking to prove one particular thing and get FDA approval to market the drug as a miracle cholesterol fighter. What other effects the drug has on the human body are largely ignored. And when clinical trial participants start showing these severe effects, they are typically “dismissed” from the trial in order to ensure that trial results look positive. In this way, extremely toxic drugs are actually approved by the FDA as “safe.”

Prescription drugs represent a war on the American people

This situation means that, right now, prescription drugs are killing 100,000 Americans each year and injuring more than two million. Those are the statistics from the Journal of the American Medical Association, and that figure doesn’t include the 40,000 or so who are killed each year by over-the-counter pain medications. These are staggering figures: it’s like having twenty-five 9/11 attacks each year, but instead of terrorists flying the airplanes, it’s pharmaceutical company CEOs. There are more deaths and injuries caused each year by pharmaceuticals than in any U.S. war or conflict since World War II.

And yet pharmaceuticals continue to be marketed as miracle drugs that can help people be healthy. But as I’ve mentioned, there are no extremely healthy people taking lots of prescription drugs!

The counter argument

The obvious counter to this argument is that people only start taking prescription drugs after they’re already sick. But that’s not true: statins are now being pushed onto perfectly healthy people who have cholesterol levels of 115, for example. They’re supposed to start taking statins as a preventative measure, even though there’s nothing wrong with them. With a similar lack of wisdom, the American Diabetes Association has recommended that all diabetics start taking statin drugs even though there is no scientifically proven benefit to doing so just in case some benefits are someday discovered!

And statin drugs are already known to cause an alarming number of dangerous side effects. After being consumed for just a few days, statin drugs start interfering with normal liver function. Within a matter of weeks or months, the patient often shows new symptoms or disorders. Upon visiting a western medical doctor, they are diagnosed with another disease or condition and — guess what? — given another prescription drug to take in combination with the statins. In the business world, this is called “upselling the customer” — getting the same customers to buy more stuff, thereby greatly increasing your profit margin.

And so it goes: one prescription after another, like boxcars on a train, until the patient is: 1) financially depleted, and 2) suffering the ravages of extreme chemical toxicity from prescription drugs. By the time a typical patient finally dies from complications caused by the prescription drugs, they may have spent $100,00 or more on drugs alone. And that number can be multiplied even further if “heroic drugs” are prescribed during the patient’s last surviving days.

Dangerous drug interactions are rarely tested

There’s another factor to consider here, too: prescription drugs are rarely tested for dangerous interactions with other drugs.In other words, even though the FDA might have approved drug A for one thing, and drug B for another, nobody ever tested what happens in human beings when both drug A and drug B are taken together. Far too often, the combination is toxic, and many prescription drug combinations are fatal. Those that are not fatal may cause other injuries, meaning they will destroy the patient’s liver or pancreas, which will of course create demand for even more prescription drugs to deal with those issues.

In this way, it’s a self-fulfilling prophecy. When you visit a western medical doctor and take even a single prescription, you’re caught in the spiral of pharmaceutical dependence. The only way to escape this trap and actually restore your health is to give up all prescription drugs and, instead, make radical changes to your diet and lifestyle– and seek out naturopathic or holistic treatments — to restore your health. This is the only way to create lasting health.

Where are all the healthy, happy, athletic prescription drug takers?

Getting back to the main point here, doesn’t it make sense that if prescription drugs made people healthy, there would be all sorts of healthy, happy, athletic people walking around touting the benefits of all the drugs they’re taking? If drugs were good for you, there should be hundreds of thousands of such people right now. They should be mentally sharp, have low body fat, high bone density, healthy digestive tracts, healthy blood chemistry, vibrant skin, high energy, excellent moods, and so on. And yet this is not at all the case.

Typically, when you meet a person who is taking multiple prescription drugs, they are overweight or obese, chronically fatigued, mentally depressed, sickly in appearance, mentally clouded, suffering from several blood chemistry problems, burdened with weak immune systems, suffering from low bone density, and emotionally unstable. Sadly, this is not only the typical prescription drug patient I’m describing here, this also describes many doctors and health care workers who dole out the drugs in the first place.

Given this reality, it takes a great leap of imagination to believe that prescription drugs are somehow good for you. 

The promise of drugs is seductive

It’s seductive, of course, to imagine that perhaps your state of mental anguish is simply a “brain chemistry imbalance” that can be corrected with antidepressant drugs. It’s tempting to treat your osteoporosis with a doctor-recommend pill rather than getting into the habit of daily walking. It’s convenient to live on heartburn medications instead of having to make healthy food choices for a change. Popping pills is always easier than changing your life, but popping pills is like making a deal with the Devil: you always end up losing.

When you take prescription drugs on a long-term basis, you’re sure to come out worse than when you started. Prescription drugs are only appropriate for short-term interventions that save a patient’s life while they make radical changes to their diet, nutrition and lifestyle that correct the underlying imbalances. For example, an obese middle-aged man suffering from extremely high cholesterol is obviously at risk of a sudden heart attack. Statin drugs might be legitimately used for a few weeks or months just to keep the guy alive while he makes radical lifestyle changes that will ultimately bring his cholesterol (and his body weight) down to reasonable levels.

The legitimate uses for prescription drugs

That’s a reasonable, legitimate use of prescription drugs. But that’s not the way they’re being promoted today. Thanks to the culture of greed and widespread lack of ethics at pharmaceutical companies, statins and other drugs are being pushed as lifetime medications while any mention of diet, nutrition or exercise is either completely avoided or, at best, glossed over. The result is that patients are told drugs are the only answer.

Doctors are culpable in this as well: most don’t even understand nutrition 101, and few bother to take the time to work with patients on lifestyle changes in the first place. Of course, most doctors would say that it’s the patients who aren’t interested in making changes, and they’re right about that, but there’s also something rather negligent about the fact that the vast majority of doctor visits result in a 90-second conversation and a prescription for the latest brand-name drug. (If you’re a medical doctor and don’t fit this description, good for you! But make no mistake: your colleagues are miserable healers…)

So why are prescription drugs so popular?

The only reason prescription drugs are so popular today is not because they work, but because they are extremely profitable. It’s profitable for the drug companies who mark them up as much as 500,000% over the cost of the raw ingredients, it’s profitable for retailers like Walgreens who mark them up even further (and whose business relies primarily on drug profits), it’s profitable for newspapers and magazines who gladly cash checks for millions of dollars in drug advertising, and it’s even profitable for doctors who receive all sorts of free vacations, “consulting fees,” and other not-so-subtle bribes in exchange for writing prescriptions for brand-name drugs.

The system is extremely profitable to everyone… everyone except you, that is. You suffer devastating health consequences when you participate. You get stuck with the medical debt. Your insurance rates go sky-high. And to add insult to injury,you’re sicker now than before you started taking the drugs!

Our system of modern medicine is a sham, folks. It’s primarily a drug racket that’s dominated by Big Pharma. The science is largely distorted (and often outright fraudulent), the ethics have all but disappeared, and the long-term price of all this is going to be enormous. We have an unprecedented problem on our hands that’s sickening an entire generation and creating stratospheric long-term health care costs for the next round of working taxpayers unlucky enough to stumble onto all this.

But don’t worry: when everybody’s sicker than ever, the drug companies will promise they have the next big cure. All you have to do is pop daily pills at $200 each, and all your health problems will be solved!

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