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Note: Explore our full index to key excerpts of revealing major media news articles on several dozen engaging topics. And don't miss amazing excerpts from 20 of the most revealing news articles ever published.

Every year, more restaurants and food companies announce that they will sell only meat produced with minimal or no use of antibiotics. And every year, despite those pledges, more antibiotics are administered to the nation's swine, cattle and poultry. According to the latest figures, released this week by the U.S. Food and Drug Administration, antibiotic sales for use on farm animals increased by 1 percent in 2015, compared to the previous year. The increase was slightly greater – 2 percent — for antibiotics used as human medicine. The FDA and other public health agencies have been pushing farmers to rely less on these drugs. Heavy use of antibiotics both in human medicine and in agriculture has led to the emergence of drug-resistant bacteria, complicating the task of treating many infections. But the FDA finds a glimmer of good news in the latest figures, pointing out that the rate of increase has slowed. In the previous year, antibiotic use had increased by 4 percent, and a total of 22 percent from 2009 to 2014.

Note: For more along these lines, see concise summaries of deeply revealing news articles about food system corruption and health

Paraquat, one of many pesticides that can’t be used in Europe but is sold in the United States and elsewhere, has been linked to Parkinson’s disease in a growing body of research. The [paraquat factory in Huddersfield, England] recently celebrated its centennial. Paraquat [is] one of the world’s most enduring weed killers - but not one that can be purchased in ... Britain or across the Channel in the rest of the European Union. So it will be sent to the United States, or another part of the globe that still allows paraquat to be sprayed on weeds. Now regulators in the United States are grappling with a wave of research linking paraquat to ... Parkinson’s disease. In a recent ... regulatory filing, the Environmental Protection Agency said, “There is a large body of epidemiology data on paraquat dichloride use and Parkinson’s disease.” The agency is weighing whether to continue allowing the chemical to be sprayed on American cropland, although a decision is not expected until 2018. In the meantime, many of the nations that ban paraquat and other chemicals whose use is contentious still allow them to be manufactured as long as they are exported to faraway fields. Even the government of China, a nation not known for environmental regulation, said in 2012 that it would phase out paraquat “to safeguard people’s lives.” As Europe and China move away from paraquat, its use is rebounding in the United States. That is particularly true for soybean fields, where the number of pounds used is up more than fourfold over the past decade.

Note: Paraquat is manufactured by Syngenta, a Swiss company known for manipulating international trade deals. For more along these lines, see concise summaries of deeply revealing news articles about corruption in government and in the corporate world.

A wide-ranging investigation into generic drug prices took its most significant turn yet on Thursday, as state attorneys general accused two industry leaders, Teva Pharmaceuticals and Mylan, and four smaller companies of engaging in brazen price-fixing schemes - and promised that more charges were coming. A civil complaint filed by 20 states accuses the companies of conspiring to artificially inflate prices on an antibiotic and a diabetes drug, with executives coordinating through informal industry gatherings and personal calls and text messages. Officials said the case was a small example of broader problems in the drug business. “We believe that this is just the tip of the iceberg,” George C. Jepsen, Connecticut’s attorney general, whose office started the inquiry that led to the charges, said. “I stress that our investigation is continuing, and it goes way beyond the two drugs in this lawsuit, and it involves many more companies than are in this lawsuit.” The complaint on Thursday describes a cozy industry culture defined by regular dinners and social outings, and argues that those events often cross the line to violate antitrust rules. Generic drug makers hoping to begin selling a new drug first seek out rivals, the suit says, in hopes of reaching an agreement on how to maintain market share and avoid competing on price. “These agreements had the effect of artificially maintaining high prices for a large number of generic drugs and creating an appearance of competition when in fact none existed,” the lawsuit says.

Note: A separate anti-trust investigation into Mylan was recently launched in New York over price-fixing on public school EpiPen contracts. For more along these lines, see concise summaries of deeply revealing Big Pharma corruption news articles from reliable major media sources.

The superbug crisis is killing more patients than breast cancer as the Government is relying on flawed figures. The Department of Health estimates that 5,000 people die each year due to drug resistance, but Dr Ron Daniels, chief executive of the UK Sepsis Trust, claims the true figure is around 12,000. The number of deaths is rising each year as more bugs that lead to blood poisoning are becoming resistant to antibiotics. The full extent of the problem is obscured because the Government statistics are calculated using “ballpark” figures from foreign studies, not those conducted in the UK. Antimicrobial resistance is considered to be one of the world’s most serious and growing long-term threats to health, which it has been warned could eventually lead to everyday cuts and infections becoming fatal. Yet superbugs are rarely listed on death certificates. The UK Sepsis Trust is calling for an official register of superbug deaths in order that the rising count is reflected in Government policy. Figures provided to The Bureau of Investigative Journalism by Dr Daniels suggest the number of people dying from sepsis, triggered by antibiotic resistant bacteria, is more than double the official figure. This would put superbugs ahead of breast cancer, which is widely thought of as one of the UK’s biggest killers, despite the number of deaths falling to 11,433 in 2014.

Note: There is strong evidence to suggest that feeding antibiotics to livestock leads to superbugs in humans. For more along these lines, see concise summaries of deeply revealing health news articles from reliable major media sources.

FBI agents arrested former Insys Therapeutics CEO Michael Babich and five other former company executives on Thursday for allegedly bribing doctors to prescribe an extremely addictive opioid painkiller to patients who didn’t need it. The Department of Justice (DOJ) alleges that the executives took part in a “nationwide conspiracy” to give healthcare providers kickbacks in exchange for the improper prescribing of Subsys - an opioid medication containing the highly addictive substance fentanyl, which is considered even more dangerous than painkillers like Vicodin. Subsys is meant to provide pain relief to cancer patients who are going through particularly excruciating pain episodes. It’s reserved for these neediest of patients due to its potency and addictive qualities. But federal prosecutors allege that Babich and his co-conspirators doled out kickbacks to doctors who prescribed the drug even to non-cancer patients, and even set up a special “reimbursement unit” to sway insurance companies and pharmacy benefits managers to provide coverage for these non-authorized uses. The charges range from racketeering to conspiracy to mail and wire fraud. The FBI’s actions come in the wake of a newly invigorated federal effort to tackle the prescription painkiller epidemic, which has claimed the lives of more than 165,000 Americans since 1999.

Note: These charges come on the heels of an ex-DEA official's public accusation that Congress has been helping drug makers avoid responsibility for their role in the US opioid epidemic. How many deaths and ruined lives are being caused by greedy executives and the politicians in their pockets? For more along these lines, see concise summaries of deeply revealing Big Pharma corruption news articles from reliable major media sources.

Boys should not be circumcised until they are old enough to choose for themselves, doctors in Denmark have said. The Danish Medical Association said it had considered suggesting a legal ban on the procedure for children under the age of 18, because it believed circumcision should be “an informed, personal choice” that young men make for themselves. When parents have their sons circumcised, it robs boys of the ability to make decisions about their own bodies ... the organisation said. Lise Mřller, chair of the Doctors' Association Ethics Board, said it was wrong to deny an individual the right to choose whether or not they wanted to be circumcised. The organisation said that because male circumcision is not without risk it should only be performed on children when there is a documented medical need. The doctors stopped short of calling for an all-out legal ban on the procedure, which is currently allowed but remains relatively rare in Denmark, because it said the move could have too many negative consequences. “We have discussed it thoroughly, also in our ethics committee," Ms Mřller said. "We came to the conclusion that it is difficult to predict the consequences of a ban – both for the involved boys, who could for example face bullying or unauthorised procedures with complications – and for the cultural and religious groups they belong to." The Danish Health and Medicines Authority estimates that somewhere between 1,000 and 2,000 circumcisions are performed in Denmark each year.

Note: Explore a treasure trove of concise summaries of incredibly inspiring news articles which will inspire you to make a difference.

A bipartisan coalition of lawmakers is rushing to finalize a new healthcare law that would overhaul the Food and Drug Administration (FDA). The bill, called the 21st Century Cures Act, is also a huge win for lobbyists: 1,455 lobbyists, working on behalf of 400 different healthcare companies, medical device makers and research institutions weighed in on the 900 pages of regulatory tweaks and research grants. Originally conceived as a bill to boost research ... pro-industry groups have used the bill as a vehicle to achieve their long standing legislative agenda. It effectively makes it easier for drug companies and medical device manufacturers to get FDA approval for their products without demonstrating that consumer safety has been taken into account. Consumer advocates are particularly concerned with several provisions that make it much easier for pharmaceutical companies to bypass stringent testing requirements to market and sell drugs for multiple uses. Currently, if a company wanted to sell a drug to treat more than one ailment, it must conduct randomized scientific trials showing the product does indeed work for each separate illness it's marketed for. The 21st Century Cures Act lowers that threshold. The bill also frees pharmaceutical companies to work with insurance companies to promote off-label uses for their drugs and creates a new category of ... medical devices which qualify for expedited regulatory approval. The lawmakers who introduced the measure are bankrolled by the healthcare industry.

Note: For more along these lines, see concise summaries of deeply revealing news articles about corruption in government and in the pharmaceutical industry.

Antibiotic resistance is a problem both for people and for livestock. But how can we be sure that the two are connected and that resistance is exacerbated by on-farm antibiotic use? In 1975 the Animal Health Institute asked this very question and recruited Tufts University biologist Stuart Levy to find out. Levy and his colleagues fed low doses of the antibiotic tetracycline to a group of 150 chickens. Within a week, almost all the E. coli bacteria in their intestines were tetracycline-resistant. Three months in ... the chickens were also resistant to four other types of antibiotics. After four months, the ... chickens on the farm that had not been fed tetracycline also harbored resistance to the drug. In 1977, soon after Levy's study was published, the FDA announced that it was considering banning several antibiotics from animal feed over safety concerns. In the 39 years since, the industry has fought hard against these plans by arguing there was no definitive proof of harm. These arguments ultimately caused the FDA to [pursue] voluntary guidances instead. Several members of the U.S. Congress, including New York State Representative and microbiologist Louise Slaughter, have introduced bills to more tightly regulate antibiotic use on farms. Slaughter has pushed for her Preservation of Antibiotics for Medical Treatment Act for more than a decade. It has been supported by 454 organizations, including the American Medical Association. But ... the bill never reaches a vote.

Note: For more along these lines, see concise summaries of deeply revealing news articles on food industry corruption and health.

After three tours in Iraq and Afghanistan, C. J. Hardin wound up hiding from the world. He had tried almost all the accepted treatments for post-traumatic stress disorder. “Nothing worked for me,” said Mr. Hardin. Then, in 2013, he joined a small drug trial testing whether PTSD could be treated with MDMA, the illegal party drug better known as Ecstasy. “It changed my life,” he said. “It allowed me to see my trauma without fear or hesitation and finally process things and move forward.” Based on promising results like Mr. Hardin’s, the Food and Drug Administration gave permission Tuesday for large-scale, Phase 3 clinical trials of the drug - a final step before the possible approval of Ecstasy as a prescription drug. The Multidisciplinary Association for Psychedelic Studies, a small nonprofit created in 1985 ... sponsored six Phase 2 studies treating a total of 130 PTSD patients. Two trials ... focused on treating combat veterans, sexual assault victims, and police and firefighters with PTSD who had not responded to traditional prescription drugs or psychotherapy. Patients had, on average, struggled with symptoms for 17 years. After three doses of MDMA administered under a psychiatrist’s guidance, the patients reported a 56 percent decrease of severity of symptoms on average, one study found. By the end of the study, two-thirds no longer met the criteria for having PTSD. Follow-up examinations found that improvements lasted more than a year after therapy.

Note: Read more about how MDMA has been found effective for treating PTSD in a therapeutic context. This FDA approval to begin Phase 3 clinical trials of MDMA suggests that the healing potentials of mind-altering drugs are gaining mainstream scientific credibility.

The Nunatsiavut government in Labrador has released a study from a Harvard mercury researcher on the effects of the newly constructed Muskrat Falls dam. The study showed that water flooding the reservoir behind the dam would contain methylmercury levels “to the point that they exceed regulatory thresholds for exposure,” building up over time in fish and other game consumed by the native population. Muskrat Falls will affect three peoples - the Innu, the Nunatsiavut and the NunatuKavut - who will have to alter their diets, and as such their cultures. Methylmercury ... can lead to intellectual impairments and immune system problems. Some of the hydroelectric dams have already disrupted the hunting and fishing traditions of the Cree living nearby. Muskrat Falls echoes what the Canadian historian James Daschuk has called “the politics of starvation.” In his 2013 study, “Clearing the Plains,” Mr. Daschuk argued that famine was a conscious settlement strategy to “create ecological conditions in which disease exploded.” Nutritional questions have always been cultural questions for the indigenous peoples of Canada. Hunting and fishing are more than a traditional way of life. The land is the connection to the larger world and to history. High methylmercury levels would render the land untrustworthy. If you cannot trust the land, what can you trust?

Note: A recent BBC article described Canada's treatment of First Nation peoples as "cultural genocide" after an official inquiry found thousands of indigenous children had died and been buried in unmarked graves after being forcibly relocated to residential schools. For more along these lines, see concise summaries of deeply revealing news articles on food system corruption and health.

Tennie White, who was prosecuted by a joint team made up of attorneys from the Environmental Protection Agency and the environmental crimes division of the Justice Department, had spent her professional life exposing contamination. She was ... particularly vocal about protecting poor African-American communities. Before she was charged and prosecuted, White had spent much of her time volunteering for [the Coalition of Communities for Environmental Justice], an organization she had co-founded to help these Mississippians contend with pollution. She traveled throughout the state ... talking about environmental issues in black communities. So in 2012, when White was charged with fraud by the EPA, the organization she so often criticized, and the charges involved a company she had helped a community challenge, [those] who had been working closely with her felt they knew exactly what had happened. “She was framed,” said [White's former colleague Rev. Steve] Jamison. “It was that simple.” I submitted a Freedom of Information Act request to the EPA for all communications relating to the investigation of Tennie White in April 2016. The agency is supposed to resolve such requests within 20 business days, but I did not receive all the documents I requested. Nor did the EPA respond to my repeated requests to address the specifics of White’s case - and why her sentence for a crime of no environmental consequence was more severe than penalties for many others who caused serious harm.

Note: Despite its mandate to protect human health and the environment, the EPA has a long history of keeping the existence of toxic waste sites secret and preventing employees from talking with congressional investigators, reporters and the agency's own inspector general. For more along these lines, see concise summaries of deeply revealing news articles on government corruption and health.

Residues of many types of insecticides, fungicides and weed killing chemicals have been found in roughly 85 percent of thousands of foods tested. Data released ... by the U.S. Department of Agriculture shows varying levels of pesticide residues in everything from mushrooms to potatoes and grapes to green beans. One sample of strawberries contained residues of 20 pesticides. Notably, the agency said only 15 percent of the 10,187 samples tested were free from any detectable pesticide residues. That’s a marked difference from 2014, when the USDA found that over 41 percent of samples were “clean” or showed no detectable pesticide residues. Prior years also showed roughly 40-50 percent of samples as free of detectable residues. Absent from the USDA data was any information on glyphosate residues, even though glyphosate has long been the most widely used herbicide in the world. The Food and Drug Administration also annually samples foods for residues of pesticides. The most recent public residue report issued by the FDA shows that violation rates for pesticide residues have been climbing in recent years.

Note: For more, see this mercola.com article. For more along these lines, see concise summaries of deeply revealing news articles on food system corruption and health.

After 30 years of immunology research, [Louis Picker] is on the verge of launching human trials for a vaccine that could stop AIDS, an epidemic that has become something of an afterthought decades after it began ravaging gay men in America. For many in the developed world, complacency has set in, largely thanks to a regimen of antiretroviral drugs that allow people with HIV to live long and healthy lives, and decades of failed attempts to develop a vaccine. In 1984, U.S. Secretary of Health and Human Services Margaret Heckler expressed hope ... that science might have a vaccine for HIV within two years. Instead, a decade passed, and by 1994, AIDS was the leading cause of death for Americans ages 25 to 44. Four vaccines have made it to human trials, but none made it to market. As Picker continued his research, scientists developed a series of antiretroviral drugs that slowly downgraded HIV to a chronic disease ... in the developed world. But globally, AIDS is still killing a lot of people, largely because most of those infected in poorer countries don't have access to the drugs. According to the World Health Organization, 1.1 million people died from AIDS in 2015. In the U.S., 50,000 new cases of HIV are reported every year. Worldwide, the number is 2 million. Every time news reports come out about Picker's research, he fields a series of phone calls from HIV-infected patients, their friends and their family. "Can I be in your trial?" people ask him. "Please, can you save my son?"

Note: How is it that COVID-19 vaccines were created just months after it became a threat while many decades later no vaccine has been found for the deadly AIDS epidemic, which according to the WHO has killed 36 million - many times the number of deaths from COVID? For more along these lines, see concise summaries of deeply revealing news articles on health from reliable major media sources.

A breathing-based meditation practice known as Sudarshan Kriya yoga helped alleviate severe depression in people who did not fully respond to antidepressant treatments, reports a new study published in the Journal of Clinical Psychiatry. Researchers found significant improvement in symptoms of depression and anxiety in medicated patients with major depressive disorder (MDD) who participated in the breathing technique compared to medicated patients who did not partake. More than half of the 41 million Americans who take antidepressants do not fully respond. Add-on therapies are often prescribed to enhance the effects of the drugs in these patients, but they typically offer limited additional benefits and come with side effects that can [prolong] the depressive episode. The meditation technique ... includes a series of sequential, rhythm-specific breathing exercises that bring people into a deep, restful, and meditative state: slow and calm breaths alternated with fast and stimulating breaths. In past studies, the practice has demonstrated a positive response in patients with milder forms of depression, depression due to alcohol dependence, and in patients with MDD; however, there are no clinical studies investigating its use for depression in an outpatient setting. Past studies suggest that yoga and other controlled breathing techniques can potentially adjust the nervous system to reduce stress hormones.

Note: Explore a treasure trove of concise summaries of incredibly inspiring news articles which will inspire you to make a difference.

On its website, Kellogg touted a distinguished-sounding "Breakfast Council" of "independent experts" who helped guide its nutritional efforts. Nowhere did it say this: The maker of Froot Loops and Frosted Flakes paid the experts and fed them talking points. The company paid the experts an average of $13,000 a year, prohibited them from offering media services for products "competitive or negative to cereal" and required them to engage in "nutrition influencer outreach" on social media or with colleagues, and report back on their efforts. For Kellogg, the breakfast council - in existence between 2011 and this year - deftly blurred the lines between cereal promotion and impartial nutrition guidance. The company used the council to teach a continuing education class for dietitians, publish an academic paper on breakfast, and try to influence the government's dietary guidelines. One of the breakfast council's most notable achievements was publishing a paper defining a "quality breakfast" in a nutrition journal. Kellogg touted the paper in its newsletter as being written by "our independent nutrition experts." Dietitians could earn continuing education credits from the publisher for taking a quiz about the paper. Kellogg didn't describe its own role in overseeing editing and providing feedback, such as asking for the removal of a line saying a recommendation that added sugar be limited to 25 percent of calories might be "too high."

Note: For more along these lines, see concise summaries of deeply revealing news articles on corruption in science and in the food system.

Seth Ellingsworth of West Richland, Washington, says he got sick in an instant last year, when he briefly inhaled a strange odor at his job at the nearby Hanford Nuclear Site. Seventy years ago, the Hanford Site produced plutonium for America's nuclear arsenal. Today, it's run by the Department of Energy through its contractor, Washington River Protection Solutions. The contractor is managing a $110 billion cleanup of 56 million gallons of chemical and nuclear waste, stored in 177 underground tanks. But the tanks are leaking, and the vapors they emit contain toxic and radioactive chemicals. Some nuclear experts have called Hanford "the most toxic place in America" and "an underground Chernobyl waiting to happen." The DOE has acknowledged in nearly 20 studies conducted over the past 24 years that there is a safety risk to workers at Hanford. But critics say the DOE ... continues to put workers at risk. Neuropsychologist Brian Campbell says he has evaluated 29 people at Hanford with both respiratory and cognitive symptoms, including "some of the worst cases of dementia that I've seen in young people." Dr. Campbell said the DOE doesn't want to acknowledge the injuries. Workers told us that "over and over," the Department of Energy and the contractor on site told them the readings for harmful materials were safe. Former workers also said that in the past they were almost never allowed to opt for protective gear, like the supplied air tanks recommended by many experts.

Note: A Newsweek article describes the Hanford site as an "American Fukushima" that will require 50 more years and $110 billion to adequately clean up. For more along these lines, see concise summaries of deeply revealing nuclear power news articles from reliable major media sources.

In every state, patient protection is supposed to be the prime directive when it comes to licensing and disciplining doctors. But a 50-state examination by The Atlanta Journal-Constitution found that only a few states have anything close to a comprehensive set of laws that put patients first. “Instead of looking out for victims or possible victims or protecting our society, we’re protecting doctors,” said Rep. Kimberly Williams, a member of the Delaware General Assembly, who sponsored a patient-protection bill last year that was blocked with a veto. The AJC studied five categories of laws in every state in the nation to determine which states are the best - and the worst - at shielding patients from sexually abusive doctors. The statutes examined covered everything from the duty to report bad doctors and the power to revoke the licenses of the worst, to the laws that decide who gets to serve on medical licensing boards and how much information consumers can know about doctors who have gotten into trouble. Not a single state met the highest bar in every category. The AJC’s findings explain how it’s possible for a doctor who has served time on felony charges, molested patients or demanded sex in exchange for prescription drugs to continue seeing patients: In most states, there’s no law against it. It often takes a horrific case or a public expose to get pro-patient legislation passed.

Note: See a list of powerful articles revealing egregious and rampant sexual abuse by doctors around the US. For more along these lines, see concise summaries of deeply revealing news articles on sexual abuse scandals and health.

Government testing for residues of an herbicide that has been linked to cancer has been put on hold, slowing the Food and Drug Administration’s first-ever endeavor to get a handle on just how much of the controversial chemical is making its way into U.S. foods. The FDA ... launched what it calls a “special assignment” earlier this year to analyze certain foods for residues of the weed killer called glyphosate after the agency was criticized by the U.S. Government Accountability Office for failing to include glyphosate in annual testing programs that look for many less-used pesticides. Glyphosate is the most widely used herbicide in the world, and is the key ingredient in Monsanto Co.’s branded Roundup herbicide line. Several private groups ... have been finding glyphosate residues in varying levels in a range of foods. Earlier this year, one of the agency’s senior chemists also analyzed glyphosate residues in honey and oatmeal and [found that some] samples contained residue levels well over the limit allowed in the European Union. The agency ... put the glyphosate residue testing part of the work plan on hold amid confusion, disagreement and difficulties with establishing a standard methodology to use across the agency’s multiple U.S. laboratories, according to FDA sources. With the testing on hold, it is not clear when the agency might have final results on the glyphosate residue analysis.

Note: Laboratory tests have shown alarming levels of glyphosate in many common foods. For more along these lines, see concise summaries of deeply revealing news articles on government corruption and health.

Essential medicines could be provided for as little as $1-$2 US a month per person in developing countries, experts said on Monday as they called on governments to boost efforts to ensure everyone can access basic healthcare. Although global spending on medicines is about eight times this amount, one in five countries spends less than $1 per month per person, according to the first analysis of the cost of providing key drugs by The Lancet Commission on Essential Medicines. The commission, comprising 21 international experts, said lack of access to affordable, quality medicines was threatening progress towards universal health coverage. The list of essential medicines contains 201 drugs needed for a basic healthcare system. The commission estimated the cost of providing essential medicines to the populations of low- and middle-income countries to be between $77 billion and $152 billion a year. It said 41 countries were spending less than $1 per person per month on medicines while global spending on medicines in 2017 was predicted to be $1.2 trillion. The experts said "massive inequities and inefficiencies" in financing and governance were restricting access to drugs for many people. They said persistent problems with the quality and safety of medicines in many low- and middle-income countries must also be addressed with better regulation, [and] called for urgent reforms in the way essential drugs are developed and patented to improve affordability and access.

Note: For more along these lines, see concise summaries of deeply revealing news articles on income inequality and health.

The Washington, D.C.-based Grocery Manufacturers Association (GMA) has been slapped with a $6 million civil penalty, which will be trebled due to its "intentional violations of state law" for laundering money in a 2013 Washington state initiative campaign. If the ... $18 million in total damages holds up on appeal, it may be the highest fine for campaign finance violations in the history of the United States. The grocery lobby group poured more than $11 million into the "No on 522" committee, which fought and narrowly defeated an initiative to require labeling of genetically modified foods and seeds sold to consumers in the state. What prompted the massive award? The GMA established what it called a "defense of brands account." It collected money to defeat the Washington initiative while shielding the identities of major food manufacturers (e.g. Pepsico, Coca-Cola, General Mills, General Foods) who were putting up millions of dollars in support. The GMA, its members and other sources had spent $43 million in 2012 to defeat California's Proposition 37, which would have required all packaged food products to identify genetically modified organisms. "While successfully defeating Prop. 37, certain individual member companies of GMA and some GMA staff received negative responses from the public because of their opposition to Prop. 37," Judge Hirsch wrote in her ruling. Hence, an elaborate scheme was hatched - and approved by the GMA's board - to conceal individual donors.

Note: Read a more in-depth, revealing article on this on mercola.com. For more along these lines, see concise summaries of deeply revealing news articles on food system corruption and the GMO controversy.

Important Note: Explore our full index to key excerpts of revealing major media news articles on several dozen engaging topics. And don't miss amazing excerpts from 20 of the most revealing news articles ever published.