Saturday, December 24, 2011

Merry Monsanto -- Military Industrial Agriculture

© unknown
Merry Monsanto -- Military Industrial Agriculture by Owen Myles

Today I read an article on slashdot titled “New Study Confirms Safety of GM Crops“. Before you navigate away from this article, please be assured they were not citing the National Enquirer. The study was conducted in France, with assistance from the usual suspects (British universities, biotechnology corporations, etc).
Also involved in the study were rodents — clearly a dietary staple of the French, and biologically (or psychologically?) identical to certain English academics.

The “evidence” cited in the study shows that — at least to monocled marsupials — GM plants are “nutritionally equivalent to their non-GM counterparts and can be safely used in food and feed.” Of course “food and feed” are not exclusive aspects of GM agriculture — or even agriculture — but corporate-sponsored research has its own perspective . . . Never mind the trace minerals and everything else!

As usual, the slashdot comments were many, and the views varied; organic versus conventional, ridicule and support of both, with lots between — all shedding light on people’s views of the subject. Admittedly, geeks may not be the best authority on such topics — often compiled of pizza and soft-drinks — but I fear they do provide an example of popular opinion regardless. Many see GM as a noble science, helping to feed the world’s growing population. Some see “organic” anthropocentrically, reducing it to a matter of pesticides, nutrition, and prices. Few seem to have a balanced perspective though.

Conventional versus organic agriculture – or where to begin:

Crop rotation gets little attention, probably due to most consumers having no familiarity with processes behind the supermarkets. Most GM crops are mono-cultures, and are rarely if ever rotated. Mono-cultures reduce biodiversity, having effects far beyond the farm, and unrotated crops stress and deplete the soil. While the terribly important subject of biodiversity is generally ignored in conventional agriculture, soil quality is maintained artificially through mined fertilizers and industrial chemicals. There are quite a few implications for this; the dust-bowl of the US, and creeping deserts of China are but a few. Artificial fertilization requires strip mining, particularly for phosphates, and the effects are harsh. Pollution of watersheds, eutrophication, devastation, and even radiation are effects of phosphate mining.

In 2003, Piney Point phosphate mine threatened to leak a hundred-plus million gallons of contaminated water into Tampa Bay. Instead of allowing it to leak, Jeb Bush authorized it to be dumped into the Gulf of Mexico. I clearly remember suffering perennial red-tide for more than a year after the first incident. In June of 2011, Piney Point threatened to leak again.

Piney Point was officially an “accident”; possibly one less expensive to pay the fines for, than to build a more secure infrastructure. But conventional agriculture is not an accident, and a look at the Mississippi Delta dead-zone is an example some of the consequences involved in run-off from fertilization.

We’ve all heard horror stories of cattle threatening to fart our beloved planet into a toxic stink-osphere. …Sure, but what they leave out is that it is not just farts, but mismanagement of the manure which produces much of this dangerous surplus of methane. Instead of properly redistributing the manure to be returned to the soil, it is often stuffed in squalid vats to putrefy without benefit — emitting methane. Could such manure not substitute these mined phosphates to some extent?

The argument that to feed the growing population we must genetically modify our crops and practice industrial agriculture is worth some attention, as it is perhaps the most popular argument supporting the industry. This argument confuses many, and irritates some like myself. One must at a minimum, consider the waste of conventional agriculture, where rather than composting and returning detritus to the soil, it is either burned, trashed, or used for other industrial purposes. Organic agriculture it is not entirely self-sufficient, but it is far more so than its contestant. Between hydroponics and more – but smaller – farms, organic (and perhaps eco-farming) could indeed maintain pace with the demands of our growing population — all while remaining far more symbiotic with ecosystems.

The French study also neglects aspects of what they claim to understand of feed. Bees are critical to agriculture, and certainly are not well hosted by conventional farms. Some studies have suggested that GM corn pollen may weaken the intestinal walls of bees, thus reducing resistance to parasites and other infections.

We know that feeding corn — as opposed to grass — to cattle increases putrefaction due to excessive starches (sugars), further leading farmers to grotesque measures; boring permanent holes into the stomachs of cows to monitor the bacterial cultures that arise from corn diets of GMO-powered starchiness, and the excessive antibiotics which become necessary as result of the intestinal imbalances caused by such diets. In humans, GM soy has been proposed to threaten intestinal flora as well, by transferring corrupted DNA into beneficial flora.

Patent-wars are another issue, and could alone make a strong case against GMOs. Whether through cross-pollination (contamination) or terminator seeds, the patent has been used to harm many farmers and sustain what would otherwise fail under fair and wholesome circumstances. Organic farming claims no ownership of nature; it seeks to work in relative harmony, and cares not to bully fellow farmers. The notorious Monsanto has been a true tyrant in this regard, litigating farmers into bankruptcy, and playing dice with biology. It is no secret that the FDA and Monsanto are close, and that neither exhibit any sincere concern for the health of the masses. They present GM science as the road to a thriving humanity, but their real motives are clearly profit — without regard to humanity’s common interests.

We also need to bring agriculture closer to home, whereever possible. By this I imply less dependence on centralized farming, and more local cooperation. The supermarket shelves can be emptied, but our yards are alive, and our greenhouses belong to us. We should be teaching ourselves the basics of growing what we can in our climates, and becoming less reliant on those who care neither about their own produce, animals, or us. Where this cannot be done, one may try to act supportively instead, whether in words or coins.

What seems objectively obvious to me is that GMOs are understudied, abused, resented by many, and will have to wait in a very long line for any truly conclusive research. Organic agriculture, however, is tried and proven — and no one resents its products. I know from experience the differences of that grown on the local farm here in Sarasota, compared to that bought in any grocery store — and they are quite apparent; from the way I feel after enjoying them, to the politics — or lack thereof — that are involved. I know of no organic farm sporting prison labor, but I can surely name a few conventional farms that do. I don’t want an institution supper, nor do I want corporate mutations in my mouth. The differences are clear, and it’s a shame that they even need be argued — but ’tis our times and tyrants.

There is much, much more to cover on this subject, though I wanted to get this out in time to wish the Activist Post readership (and syndicates) a Merry Christmas for all those who celebrate it, and the kindness of the holiday spirit to everyone, which will hopefully some day no longer be once per year.

Map of Florida’s Bone Valley: www.baysoundings.com/sum05/BoneValley.pdfOwen Myles writes and edits the Eccentric Intelligence Agency: Helping the Ouroboros finish itself.

Occupy The Holidays

Occupy The Holidays



We partnered with the OWS Interfaith group Occupy Faith, the Yes Men and the Posterboy Collective to create this holiday video that documents the symbolic gift of a nativity scene to Trinity Church and inspires debate about the role of faith in social movements.

Nativity Scene by PosterBoy (http://www.flickr.com/photos/26296445@N05/)
http://www.occupyfaith.com
http://www.yeslab.org/trinity
http://www.occupywallst.org

"I Cannot Eat Your Prayers": How Student Debt Changed One Woman's Mind on "Christian Charity"

© Jasmic
"I Cannot Eat Your Prayers": How Student Debt Changed One Woman's Mind on "Christian Charity" by Kristin Rawls

From an evangelical home to over $100,000 in student loans and healthcare debt, one writer faces the ways in which even progressive Christianity comes up short. 

 I'm going to tell you a story. It's the story of a good girl from a quiet town who prayed, studied hard, said no to drugs, and otherwise did everything she was told - and then went on to become Sallie Mae's bitch and lost just about everything. This story is mine.

I grew up in an evangelical home, and was an earnest "liberal-evangelical" into my early twenties. Now I think that my former religious faith - not unlike my faith in the U.S. higher education system - gave me a warped sense of optimism about the way the world works. I believed in faith-based platitudes, plus a few secular ones. Examples:
  1. God has a plan for my life.
  2. My whole future is ahead of me.
Until a few days ago, I was too ashamed to talk publicly about what happened to me. That's when I saw Natalia Antonova's incredibly brave piece at Alternet detailing her pending student loan default. This issue is so cloaked in shame and humiliation that many of us stay silent. Check out Natalia's post-article / blog post if you don't think stigma and shame are deeply intertwined with defaulting on debt out of necessity: she has been contacted by people who say they hope her lenders drive her to suicide.

This attitude is deeply engrained in many of us. Financial struggle is associated with sloth in this country. (Thank you, Newt Gingrich, for reminding me of that so frequently these days.) I have a very low credit score, and this means I have had trouble finding stable employment. So I go from temporary job to temporary job and write as many freelance articles as I can convince anyone to pay me for.

Read complete article..


Comment: I've added Dominion to the analecta as this is a marker for the people that Kristin describes who have been corralled by Satan himself and are described in the lexicon associating the calends and class and exists as moon shine in a manner of speaking. Please read the entire article and her complete story.

Traditional medicine offers a “revolution” in Tanzanian healthcare

© ANH
Traditional medicine offers a “revolution” in Tanzanian healthcare - ANH

While other semi-industrialised countries, like India or Brazil, are pinning considerable hope for their economic futures on their booming generic (unbranded) pharmaceutical industries, a different option is about to be explored in one part of Africa. Tanzania’s National Institute for Medical Research (NIMR) recently announced that several unique remedies based on traditional herbal medicines are about to enter the approvals system – and could be in mass production within 6 months.

Harnessing ancient knowledge to fight modern diseases


The Tanzanian programme superficially appears most similar to the ‘phytopharmaceutical’ method of herbal medicine production, which emerged from Germany 50 or more years ago. At this stage, we do not know whether the new Tanzanian herbal remedies are based on purified extracts of herbs, as is the case with phytopharmaceuticals, or on whole-herb material. What we do know is that 11 years of research by NIMR, beginning in 2000, has resulted in a range of ‘modernised’ traditional medicines, all based on indigenous Tanzanian herbs and available in various formulations: from Persican for control of diabetes and cholesterol, to Warburgistat for opportunistic infections in HIV/AIDS patients and TMS 2001 for malaria and fever. (Note that these trade names may change before the products come to market.)

Dr Julius Massanga, NIMR’s director for research co-ordination and promotion, is hopeful that the new range will begin mass production soon. “After registration by the TFDA [Tanzania Food and Drugs Authority], which I hope will happen soon, the next step will be to invite prospective investors followed by construction of a factory.”

A medical model for the masses


Dr Massanga passionately believes that ordinary Tanzanians should have the opportunity to choose between Western, orthodox allopathic medicine and forms of traditional healing. In a situation that rings bells for many of us, traditional medicine has been portrayed as outdated and ineffective in Tanzania since its independence, when Western medicine came to the forefront. Yet more evidence that the anti-natural healthcare crusade has tentacles everywhere!

One of the most important aspects of the new treatments will be their relatively low cost compared with orthodox medicines, Dr Massaga told ANH-Intl. A process of collaboration and research, led by the NIMR, has resulted in medicines that combine herbs used by traditional healers for centuries with other medicinally useful plants identified by the research programme. Indigenous herbs mean minimal production costs, which will be passed on to patients. For Dr Massaga, the new treatments maintain herbal medicine as the medicine of the people, while updating it for the 21st century.

The spectre of sustainability


According to Dr Massaga, all the herbs used in the new products will be collected from the wild. Such ‘wildcrafting’ ensures that the herbs are growing in their natural habitat, and can ensure optimum product quality if done correctly – but it also brings its own set of problems. Perhaps most pressingly, it’s very easy to over-harvest a habitat unless great care is taken, raising significant questions around long-term sustainability.  It is, therefore, vital for sustainability issues to remain firmly on the agenda and to be central for any prospective investors. In the past, when other African countries tried to strike out on their own traditional medicinal road, Big Pharma eventually got in on the act: either because it saw a potential market disappearing, or worse still, identified the potential for a major ‘natural health’ success story. For the sake of Tanzania’s delicate ecosystem and its cultural heritage, we hope that new investment partners see the opportunity to do something different and positive for the country’s healthcare, and support the programme without imposing any tainted agenda of their own.

Tanzania shows another way forward


It’s early stages, but it seems to us that Tanzania’s commitment to try something a little different from the norm is to be applauded and supported. We can only hope that the new medicines are successful in giving the Tanzanian people a cheaper, effective alternative to the medical orthodoxy and its pathological desire for a worldwide monopoly on healthcare.

Friday, December 23, 2011

Smart Meters Make Themselves At Home . . . by Force

Smart Meters Make Themselves At Home . . . by Force by Heather Callaghan

Many Idaho residents want nothing to do with the new Smart Meters forced on them by Idaho Electric and the Public Utilities Commission in order to replace analog electric meters.

Some simply don't want them, others don't appreciate the eerie surveillance of residents' whereabouts and usage and the ability for remote power shut-off, especially where medical devices are concerned.

Most alarming have been the health effects from the EMF output – headaches, insomnia, nausea, ringing ears and more reported by residents nationwide.

Idaho Electric has been caught installing Smart Meters without permission, despite protest, even hopping fences while residents are away. Whether residents are home or not, IE reps have brought armed law enforcement to make sure the job gets done and police go without questioning or filing paperwork.

The media has been strangely quiet about the incidents and the outraged residents. One reporter interviewed an investigative blogger who brought the incidents to light, and wanted to clear it with her editor first. The story never made it to the papers. If anything, the mainstream media have lauded the new “energy efficient” Smart Meters despite growing evidence of health hazards and power spying.

do it yourself solar power kits
Advertisement
On the one hand, IE says they would never force them on anyone (they just bring cops for good luck?), yet most utility companies and their bedfellow Public Utility Commissioners are calling them mandatory. They're not. And corporations are not allowed to bypass local officials and those they serve with mandates anyway.

Meanwhile, in Santa Cruz, CA, PG&E has resorted to another tactic of force – electricity shut-offs. And two weeks before Christmas to really tighten the screws. This time the media was there and PG&E was compared to both Scrooge and The Grinch Who Stole Christmas.

Local customers had pleaded with PG&E for weeks to have their Smart Meters removed, some installed without their knowledge. These residents were facing some serious health effects like insomnia, nosebleeds and nausea. After not being heard, they finally resorted to having professional electricians replace them with analog meters. So, naturally, PG&E shut their electricity off with no notice and no hope for their power back anytime soon.

Some of these paying customers had small and ill children who had to stay with relatives due to having no heat in freezing temperatures, and others had medical issues that required electricity for devices. Ironically, PG&E blames the action on the “public health safety risk” of having an electrician remove the meter.

Their choices were: no power, Smart Meter, or a digital meter which also emits EMF and causes health problems. A rep explained that the residents were supposed to call to get on a delay line until some opt-out method was developed, which would be weeks and weeks away. From the sounds of this “mandate,” any kind of opt-out will prove nearly impossible -- it already has. There were also hefty fees associated with any opt-outs which made PG&E look much better.

Thankfully, this type of corporate retaliation brought forth disgust and wrath from Santa Cruz public officials who intervened to help the families.

In a board meeting, they grill a PG&E pawn, and school her on her company's indefensible and non-sensical actions. They wanted answers and wouldn't accept her vague ramblings. They wanted to know exactly who to contact that could actually make a decision for the residents with no power. NOW -- not six weeks from now when some opt-out or delay decision made it down the ladder.

This board meeting is a must-see! Local government at its finest -- actually stepping in to protect individual liberty.

In one memorable part, a board member compares this corporation's actions to bankers pretending to help homeowners with mortgage questions, but systematically making sure they never talk to the same rep, sending them all over the place, and never actually helping their paying customers.

“We're having a Dickens moment here,” says one member. “You can choose to be Scrooge or you can say 'Let's get into the spirit of the holidays and help someone in need.'” A someone, who, by the way, is paying for this service! Another member wanted a different situation corrected: a resident said “No” to the Smart Meter, but it was installed anyway.

Amish Dairy Farmer Selling Raw Milk Won’t Be Cowed by FDA

© unknown
Amish Dairy Farmer Selling Raw Milk Won’t Be Cowed by FDA by Michael Tennant

Milk may do a body good, but selling it without the government’s stamp of approval does not. Dan Allgyer, an Amish dairy farmer, is finding that out the hard way. The federal government is trying to slap a permanent injunction on him preventing him from selling his cows’ product to willing customers in other states — all because Allgyer and his customers prefer to trade in milk that has not been pasteurized.

The sale of unpasteurized, or raw, milk is legal in Pennsylvania, where Allgyer lives. In Maryland, where some of his customers live, it is not. The Food and Drug Administration has decided that interstate sales of raw milk, particularly when the state for which the milk is destined bans its sale, are illegal; and that is why Allgyer now finds himself in hot moo juice with the feds.

Currently a food-buying club in Maryland called Grassfed on the Hill sends a truck to Allgyer’s farm to purchase and pick up his milk. They then transport it back to their home state, where it is distributed to club members in private homes. Allgyer is not personally selling the milk in Maryland at all.

The FDA, whose headquarters are in Silver Spring, Maryland, apparently got wind of this arrangement and launched an investigation. The agency spent over a year and countless tax dollars on an undercover infiltration of Grassfed on the Hill. Its agents joined the club under assumed names, placed orders for milk, and went into private residences to pick up their purchases. Then the FDA conducted an armed, pre-dawn raid on Allgyer’s farm in April 2010, during which agents found raw milk coolers marked for various destinations in Maryland. Now it had all the evidence it needed to prove that Allgyer was engaged in the dastardly act of selling raw milk across state lines.

The Department of Justice is asking U.S. District Court Judge Lawrence Stengel for summary judgment to impose the injunction on Allgyer. All the judge has to do is sign the government’s ready-made form, and Allgyer will be banned from ever selling his milk to folks from out of state again, at which point he will be “essentially … out of business,” according to raw-milk advocate David Gumpert.

Actually, he doesn’t just get to be put out of business. The proposed injunction provides for the added privilege of having his farm inspected whenever FDA agents are bored or just have the urge, AND he gets to pay big time for the privilege (at rates of $87.57 or $104.96 per hour, plus 51 cents a mile for their travel, plus the regular government “per diem” for meals and hotels). One inspection that lasts a day or two, and involves two or three agents, who, of course, have to write up a detailed report afterwards, could cost $10,000. Maybe they decide to do it once a year, maybe once a month, maybe once a week. Whatever their pleasure.

At the end of five years, Allgyer can tell the court he’s been a good boy, and appeal to have the injunction lifted, and maybe it will be and maybe it won’t. If not, the inspection arrangement continues.

survival seed vault
Advertisement
Gumpert takes issue with a number of the “undisputed facts” in the government’s case. For one thing, the government asserts that Allgyer’s arrangement with the food club amounts to interstate commerce; yet the food was purchased in Pennsylvania and driven to Maryland by the organization that had purchased it, where it was then distributed to members. The commerce took place entirely within the bounds of the Keystone State.

In addition, the government leaves out some crucial information. It points out that “a few state courts have addressed” the matters of private food clubs and cow-share arrangements (in which individuals purchase shares in cows and receive the cows’ raw milk in return) but cites only the case in which Wisconsin ruled against such arrangements, conveniently omitting another case in which Ohio ruled in favor of them.

Furthermore, while the FDA says that it tested 12 samples of Allgyer’s milk to confirm that it was unpasteurized, it neglects to mention that those tests, whose results Gumpert obtained via a Freedom of Information Act request, also showed that the milk was safe to drink, undercutting the FDA’sargument that “drinking raw milk is dangerous and [it] shouldn’t be consumed under any circumstances.”

Allgyer is fighting back with what Gumpert calls “a credible and cogent response” to the FDA’s motion for summary judgment.

Allgyer makes several arguments as to why summary judgment should be denied and he be given his day in court. First he argues that his arrangement with Grassfed on the Hill is a private agreement not subject to the FDA, citing some Supreme Court decisions to buttress his case. Allgyer also contends that the case is not “a civil matter” but “a quasi-criminal matter because of the severe sanctions and consequences that could occur as a result.” Therefore, he maintains, he is entitled to due process of law, especially since “there was no probable cause to even file a complaint in this instant case.” As Gumpert summarized the argument, “trying to stamp out a small enterprise should require more careful judicial consideration than just signing a pre-printed FDA order form.”

Allgyer further argues that the FDA has not answered Privacy Act questions as required by law, which means that “the information and excessive data [the FDA has] obtained to date from [its] inspections are tainted and cannot be used against us in any matter.” He states that under FDA laws and regulations the warning letters he received from the FDA are not permitted as part of an investigation and should thus be “rescinded, cancelled, abated, and voided.” Finally, he writes that he “requested the oaths of office of the agents involved and did not receive them,” but such oaths must by law be taken and filed or else those agents have no authority to investigate anyone.

Claiming that the FDA’s actions have “created a serious dilemma” for him by violating his rights to due process and equal protection under the law, Allgyer makes one final plea for denial of summary judgment, concluding, “The Defendant is prepared to proceed with a public court forum, if necessary.” This, Gumpert notes, is a step most Amish take very reluctantly; but he also believes that Allgyer has good reason to take it:

The FDA obviously wants to avoid a public confrontation with an Amish farmer, which is why it filed a written motion for summary judgement [sic] in the first place. It hoped the judge would simply sign its pre-printed Permanent Injunction, allowing the big-shot Justice Department lawyers to walk away without having to confront their prey. No, a public hearing, with a humble dairy farmer making his own defense, in front of a courtroom full of buying club supporters, is not what the FDA had in mind when it launched this case last April.

With any luck, however, that is exactly what it is going to get. Then maybe Allgyer and others who in one form or another defy the FDA’s unconstitutional ban on interstate raw milk sales will be vindicated as well.

You Are The Battlefield!

You Are The Battlefield! - Activist Post

Health Benefits of Turmeric

© healthjockey.com
Health Benefits of Turmeric

 The active ingredient in turmeric is curcumin. Tumeric has been used for over 2500 years in India, where it was most likely first used as a dye.

The medicinal properties of this spice have been slowly revealing themselves over the centuries. Long known for its anti-inflammatory properties, recent research has revealed that turmeric is a natural wonder, proving beneficial in the treatment of many different health conditions from cancer to Alzheimer's disease.

Here are 20 reasons to add turmeric to your diet:
  1. It is a natural antiseptic and antibacterial agent, useful in disinfecting cuts and burns.
  2. When combined with cauliflower, it has shown to prevent prostate cancer and stop the growth of existing prostate cancer.
  3. Prevented breast cancer from spreading to the lungs in mice.
  4. May prevent melanoma and cause existing melanoma cells to commit suicide.
  5. Reduces the risk of childhood leukemia.
  6. Is a natural liver detoxifier.
  7. May prevent and slow the progression of Alzheimer's disease by removing amyloyd plaque buildup in the brain.
  8. May prevent metastases from occurring in many different forms of cancer.
  9. It is a potent natural anti-inflammatory that works as well as many anti-inflammatory drugs but without the side effects.
  10. Has shown promise in slowing the progression of multiple sclerosis in mice.
  11. Is a natural painkiller and cox-2 inhibitor.
  12. May aid in fat metabolism and help in weight management.
  13. Has long been used in Chinese medicine as a treatment for depression.
  14. Because of its anti-inflammatory properties, it is a natural treatment for arthritis and rheumatoid arthritis.
  15. Boosts the effects of chemo drug paclitaxel and reduces its side effects.
  16. Promising studies are underway on the effects of turmeric on pancreatic cancer.
  17. Studies are ongoing in the positive effects of turmeric on multiple myeloma.
  18. Has been shown to stop the growth of new blood vessels in tumors.
  19. Speeds up wound healing and assists in remodeling of damaged skin.
  20. May help in the treatment of psoriasis and other inflammatory skin conditions.
Turmeric can be taken in powder or pill form. It is available in pill form in most health food stores, usually in 250-500mg capsules.

Once you start using turmeric on a regular basis, it's fun to find new ways to use it in recipes. My favorite way to use it is to add a pinch of it to egg salad. It adds a nice flavor and gives the egg salad a rich yellow hue.

Contraindications: Turmeric should not be used by people with gallstones or bile obstruction. Though turmeric is often used by pregnant women, it is important to consult with a doctor before doing so as turmeric can be a uterine stimulant.

Related:

Turmeric: The Return of The Golden Goddess

Thursday, December 22, 2011

Visions of Angels Described in Bible May Have Been Lucid Dreams

© Public domain
Elijah and the Angel by Bernardino Luini (1521).
Dec. 21, 2011: Visions of Angels Described in Bible May Have Been Lucid Dreams by Natalie Wolchover

Sleep researchers say they have established that many of the visions of angels and other religious encounters described in the Bible were likely "the products of spontaneous lucid dreams."

In a sleep study by the Out-Of-Body Experience Research Center in Los Angeles, 30 volunteers were instructed to perform a series of mental steps upon waking up or becoming lucid during the night that might lead them to have out-of-body experiences culminating in perceived encounters with an angel. Half of them succeeded, the researchers said.

Specifically, the volunteers were told to try to re-create the story of Elijah, a prophet who is referenced in the Talmud, the Bible and the Quran. In one of the stories in the Bible's Book of Kings, Elijah flees to the wilderness and falls asleep under a juniper tree, exhausted and prepared to die. Suddenly an angel shakes him awake and tells him to eat. He looks around and, to his surprise, sees a loaf of bread baked on some coals and a jug of water. Elijah eats the meal and goes back to sleep. Lead researcher Michael Raduga said this event was chosen from among a multitude of biblical passages involving religious visions during the night, because, "in terms of verifiable results, angels were the ideal choice, as Western culture provides a relatively well-established image for them (wings, white robes, halos, etc.)."

The research, which has not been reviewed by peers for scientific publication, does garner support from some dream researchers who were not involved in Raduga's study. They said the findings support further inquiry into the basis of such religious visions. One dream expert, however, pointed out that many religious tales of angelic encounters occurred in daytime, which suggests they could not have been dreams.

Dreaming of Elijah

During the four weekends devoted to the study, 24 of the volunteers indicated they had experienced at least one lucid dream. They had been instructed to try to "separate from their bodies" every time they became half-awake or lucid during the night. If they were able to dream that they had separated from their sleeping bodies, they were then supposed to look for angels in their homes. If they were unable to have an out-of-body dream experience, they were told to go back to sleep and try again later in the night.

Fifteen of the 24 "lucid" participants said they were able to re-create the story of Elijah during their dreamlike experiences, either in part or in full. Nine of them dreamed of experiences involving both an angel and food, while the other six encountered only an angel.

Raduga, whose organization is partly funded by sales of his "practical guide" books on lucid dreaming, designed the experiment to test his theory that many reports of miraculous encounters are actually instances of people experiencing this vibrant, lifelike dream state. If he could coach people to dream a realistic religious encounter, he said, that could prove that many historical accounts of such encounters - such as Elijah's vision in the Bible - are really just products of people's imaginations.

Angelic encounters

The volunteers who succeeded in envisioning angels described their encounters for the researchers.

One participant, identified as Anton M., recalled making a successful attempt to separate from his body: "I left my body and then summoned my 'guide,' and he came in the form of an angel. I asked him for some cookies and water. He gave them to me readily. I ate everything up, experiencing every taste sensation and the feeling of satiation. I returned to my body and fell right back asleep."

Though Raduga and his colleagues' work has not been peer-reviewed or published, other dream researchers called the findings interesting and suggestive. "I am sure these guys are on to something," said Allan Hobson, a professor emeritus of psychiatry at Harvard Medical School and author of several books on the neuroscience of dreaming, including Dream Life (MIT Press, 2011).

Hobson said the idea that religious encounters were actually vivid dreams isn't new. "William James, the great and very tolerant philosopher-psychologist, wrote a book in 1912 entitled Varieties of Religious Experience in which he stated that many visions were probably dreamlike apparitions," he told Life's Little Mysteries in an email.

And then there is "the story of Emmanuel Swedenborg, the Swedish scholar, who ... sleep-deprived himself, and it wasn't long before the angels appeared and told him to found the Church of the New Jerusalem," Hobson said.

Ursula Voss, a sleep and dreaming psychologist at the University of Bonn in Germany, agrees that some religious encounters could be products of the human mind. "But other scenarios are also possible," Voss said. If the visions are imagined, she argues that these encounters would not happen during lucid dreaming, but instead could be examples of "hypnagogic hallucinations," which happen just before people fall asleep, when the brain is highly susceptible to the power of suggestion.

Brigitte Holzinger, a psychologist at the Institute for Consciousness and Dream Research who was not involved in Raduga's study, said that many biblical tales are recorded as having happened during the day; as such, they were probably not dreams.

"What we can learn from this is that we need a better definition of lucid dreaming, and based on that definition we need to distinguish lucid dreams from other forms of trances, visions and maybe even hallucinations," Holzinger wrote in an email.

She added that "a project trying to determine these states would be very interesting."

Nuke Expert/MD: Japan Government Was Lying Through its Teeth About Fukushima... and Probably Still Is

© n/a
Japanese child being screened for radiation.
Nuke Expert/MD: Japan Government Was Lying Through its Teeth About Fukushima... and Probably Still Is

 CMAJ: Public Health Fallout from Japanese Quake, Canadian Medical Association Journal, Dec. 21, 2011:

A "culture of cover up" and inadequate cleanup efforts have combined to leave Japanese people exposed to "unconscionable" health risks nine months after last year's meltdown of nuclear reactors at the Fukushima Dai-ichi power plant, health experts say. Although the Japanese government has declared the plant virtually stable, some experts are calling for evacuation of people from a wider area, which they say is contaminated with radioactive fallout.

They're also calling for the Japanese government to reinstate internationally-approved radiation exposure limits for members of the public and are slagging government officials for "extreme lack of transparent, timely and comprehensive communication."

But temperatures inside the Fukushima power station's three melted cores have achieved a "cold shutdown condition," while the release of radioactive materials is "under control," according to the International Atomic Energy Agency. That means government may soon allow some of the more than 100,000 evacuees from the area around the plant to return to their homes. They were evacuated from the region after it was struck with an 8.9magnitude earthquake and a tsunami last March 11.

Although the potential for further explosions with substantial releases of radioactivity into the atmosphere is certainly reduced, the plant is still badly damaged and leaking radiation, says Tilman Ruff, chair of the Medical Association for Prevention of Nuclear War, who visited the Fukushima prefecture in August.
"There are major issues of contamination on the site. Aftershocks have been continuing and are expected to continue for many months, and some of those are quite large, potentially causing further damage to structures that are already unstable and weakened. And we know that there's about 120,000 tons of highly contaminated water in the base of the plant, and there's been significant and ongoing leakage into the ocean."
The full extent of contamination across the country is even less clear, says Ira Hefland, a member of the board of directors for Physicians for Social Responsibility.
"We still don't know exactly what radiation doses people were exposed to [in the immediate aftermath of the disaster] or what ongoing doses people are being exposed to. Most of the information we're getting at this point is a series of contradictory statements where the government assures the people that everything's okay and private citizens doing their own radiation monitoring come up with higher readings than the government says they should be finding."
Japanese officials in Tokyo have documented elevated levels of cesium - a radioactive material with a half-life of 30 years that can cause leukemia and other cancers - more than 200 kilometres away from the plant, equal to the levels in the 20 kilometre exclusion zone, says Robert Gould, another member of the board of directors for Physicians for Social Responsibility.

International authorities have urged Japan to expand the exclusion zone aroundthe plant to 80 kilometres but the government has instead opted to "define the problem out of existence" by raising the permissible level of radiation exposure for members of the public to 20 millisieverts per year, considerably higher than the international standard of one millisievert per year, Gould adds.

This "arbitrary increase" in the maximum permissible dose of radiation is an "unconscionable" failure of government, contends Ruff.
"Subject a class of 30 children to 20 millisieverts of radiation for five years and you're talking an increased risk of cancer to the order of about 1 in 30, which is completely unacceptable. I'm not aware of any other government in recent decades that's been willing to accept such a high level of radiation-related risk for its population."
Following the 1986 nuclear disaster at the Chernobyl nuclear power plant in the Ukraine, "clear targets were set so that anybody anticipated to receive more than five millisieverts in a year were evacuated, no question," Ruff explains. In areas with levels between one and five millisieverts, measures were taken to mitigate the risk of ingesting radioactive materials, including bans on local food consumption, and residents were offered the option of relocating. Exposures below one millisievert were still considered worth monitoring. In comparison, the Japanese government has implemented a campaign to encourage the public to buy produce from the Fukushima area, Ruff added. "That response [in Chernobyl] 25 years ago in that much less technically sophisticated, much less open or democratic context, was, from a public health point of view, much more responsible than what's being done in modern Japan this year."

Were Japan to impose similar strictures, officials would have to evacuate some1800 square kilometres and impose restrictions on food produced in another 11,100square kilometres, according to estimates of the contamination presented by Dr. Kozo Tatara for the Japan Public Health Association at the American Public Health Association's 139th annual meeting and exposition in November in Washington, District of Columbia.

"It's very difficult to persuade people that the level [of exposure set by the government] is okay," Tatara told delegates to the meeting. He declined requests for an interview.The Japanese government is essentially contending that the higher dose is "not dangerous," explains Hefland. "However, since the accident, it's become clear the Japanese government was lying through its teeth, doing everything it possible could to minimize public concern, even when that meant denying the public information needed to make informed decisions, and probably still is."

"It's now clear they knew within a day or so there had been a meltdown at the plant, yet they didn't disclose that for weeks, and only with great prodding from the outside," Hefland adds. "And at the same moment he was assuring people there was no public health disaster, the Prime Minister now concedes that he thought Tokyo would have to be evacuated but was doing nothing to bring that about."

Ruff similarly charges that the government has mismanaged the file and provided the public with misinformation. As an example, he cites early reports that stable iodine had been distributed to children and had worked effectively, when, "in fact, iodine wasn't given to anyone."

Public distrust is at a level that communities have taken cleanup and monitoring efforts into their own hands as the government response to the crisis has been "woefully inadequate" and officials have been slow to respond to public reports of radioactive hotspots, Gould says. "That's led to the cleanup of some affected areas, but there are also reports of people scattering contaminated soil willy-nilly in forests and areas surrounding those towns." "In some places, you can see mounds of contaminated soil that have just been aggregated under blue tarps," he adds.

Even with government assistance, there are limits to the decontamination that can be achieved, explains Hefland. "What do you do with the stuff? Do you scrape entire topsoil? How far down you have to go? And if you wash down the buildings, what do you do with the waste water?"

As well, Ruff argues the government must examine the provision of compensation for voluntary evacuation from areas outside of the exclusion zone where there are high levels of radioactive contamination. Without such compensation, many families have no option but to stay, he says. "At this point, the single most important public health measure to minimize the health harm over the long term is much wider evacuation."

The Japanese government did not respond to inquiries.

Lauren Vogel,CMAJ, with files from Barbara Sibbald, CMA

Madness: Even School Children Are Being Pepper-Sprayed and Shocked with Tasers

© alternet.org
Madness: Even School Children Are Being Pepper-Sprayed and Shocked with Tasers by Rania Khalek

An alarming series of incidents offers some insight into how casual police have become about deploying "less lethal" weapons.

There is something truly disturbing about a society that seeks to control the behavior of schoolchildren through fear and violence, a tactic that harkens back to an era of paddle-bruised behinds and ruler-slapped wrists. Yet, some American school districts are pushing the boundaries of corporal punishment even further with the use of Tasers against unruly schoolchildren.

The deployment of Tasers against “problem” students coincides with the introduction of police officers on school campuses, also known as School Resource Officers (SROs). According to the Los Angeles Times, as of 2009, the number of SROs carrying Tasers was well over 4,000.

As far back as 1988, the American Academy of Child and Adolescent Psychiatry, National Congress of Parents and Teachers, American Medical Association, National Education Association, American Bar Association, and American Academy of Pediatrics recognized that inflicting pain and fear upon disobedient children is far more harmful than helpful. Yet, we continue to do it with disturbing results, despite mountains of evidence of more effective methods of discipline.

Read complete article..

Frito-Lay sued for labeling its GMO-filled snacks as “All Natural”

NOT NATURAL
Frito-Lay sued for labeling its GMO-filled snacks as “All Natural” by Rady Ananda

Less than a year after Frito-Lay announced plans to make half their products without “any artificial or synthetic ingredients,” the $13 billion company was sued last week in federal court for fraudulently marketing the snacks that contain genetically modified ingredients.

Somehow, “artificial” and “synthetic” doesn’t include “genetically modified” in Frito’s mind.

In its April 2011 “Seed-to-Shelf” disclosure campaign, Frito-Lay promised to inform consumers about each individual snack’s ingredients, even setting up an app for smartphone users to swipe the product’s barcode and read about it. Ann Mukherjee, Frito-Lay’s senior vice president and chief marketing officer, gushed:

“What better way to share the story behind Frito-Lay snacks than by giving consumers a look inside our Flavor Kitchen to see first-hand the all natural ingredients and real foods that inspire the products we make?”

Real foods?  All natural?  Even Monsanto defines genetically modified organisms as unnatural, which the lawsuit quoted: “Genetically Modified Organisms (GMO) – Plants or animals that have had their genetic makeup altered to exhibit traits that are not naturally theirs.”


The World Health Organization agrees, defining GMOs as “organisms in which the genetic material (DNA) has been altered in a way that does not occur naturally.”

The lawsuit names only one plaintiff, Julie Gengo of Richmond, California, but includes all those who purchased Frito’s products which bear the “ALL NATURAL” label.  Last August, the law firm Milberg LLP invited potential litigants to contact them.

Though Gengo holds a BS in Electrical Engineering, she earns a living as an independent marketer for such organizations as Berkeley Playhouse/Julia Morgan Center for the Arts, Vital Systems, Bay Area Green Tours, Oxfam America and Slow Money Northern California. She describes herself as “an ongoing environmental, and healthy foods advocate.”

In early 2009, she wrote Genetically Modified (GM) Foods – Another Reason to Buy Organic, warning people that Frito-Lay uses GMOs.  According to the complaint, since 2007, she regularly bought the company’s Tostitos and Sun Chips believing they were “all natural” as indicated in advertising and on the package.

On Dec. 20, Frito’s “Naturally Delicious” webpage still boasts: “All Frito-Lay snack chips made with natural ingredients start with all-natural corn or potatoes and healthier oils. For our flavored LAY’S®, TOSTITOS® and SUNCHIPS® products, we are using all natural seasonings that don’t have artificial or synthetic ingredients.”

But because they contain GMOs from genetically modified corn and genetically modified soy, in five separate counts, plaintiff charges Frito-Lay with fraud, deception, unfair competition and false warrants under several laws including the federal Magnuson-Moss Warranty Act.

Based in New York City and specializing in class-action lawsuits on behalf of investors and consumers, Milberg LLP also has offices in Los Angeles, Tampa and Detroit. Founded in 1965, the firm now employs about 75 attorneys.

After two successful class action suits against military contractors Raytheon and General Electric, in 2006 Milberg was the target of a criminal probe by the US Dept of Justice. The firm and some of its partners were indicted on 20 criminal counts including bribery, racketeering and fraud. The DOJ press release alleges the firm participated “in a scheme in which several individuals were paid millions of dollars in secret kickbacks in exchange for serving as named plaintiffs in more than 150 class-action and shareholder derivative-action lawsuits.”

Four of Milberg LLP’s partners served time in prison, and the firm paid $75 million in fines before the DOJ dropped the matter, reports Wikipedia.

Frito-Lay North America is a wholly-owned subsidiary of PepsiCo, Inc. Though Pepsi uses genetically modified sweeteners (high fructose corn syrup) in its soft drinks, it does not label them for U.S. consumers, adhering to the US regulator policy of hiding GMOs from the public.

In 2009, the US Food and Drug Administration proposed rules banning GMO labels. Despite government policy of keeping GMO food ingredients secret from the public, citizens are advancing toward requiring full disclosure.

  • The Frito-Lay lawsuit was initiated in California where a GMO-label law has been proposed for vote in the November 2012 election.
  • In Ohio, a district court overturned the ban on labeling milk as free from artificial hormones last year.  The FDA approves the genetically modified additive, which has been linked to cancer and lower milk quality. Developed by Monsanto, rBGH is banned in Canada, the European Union, Japan and Australia.
I have to admit I still enjoy a bag of Fritos every now and then, a victim of high school euphoric recall when we would smoke a bowl and then eat Fritos, washing them down with cold chocolate milk.  (What a body rush.)  Still, I want the packages labeled.  A better snack is hand-made eggrolls, with completely organic ingredients and sauce. You can find that recipe in Cooking Close to Home.  I even found a package of eggroll wraps (at Whole Foods Market) that advised the product was made without GMOs.  Na na na to the FDA.

Rady Ananda is an independent reporter specializing in Natural Resources. Please visit and support her websites Food Freedom and COTO Report. Follow her on Twitter.

Wednesday, December 21, 2011

Genetically Modified HIV Vaccine Approved - Human Tests to Begin Shortly

© Natural Society
Genetically Modified HIV Vaccine Approved - Human Tests to Begin Shortly by Mike Barrett

At a further attempt to halt the spread of HIV, the United States is making a bold and extremely risky decision. Researchers from the University of Western Ontrario developed a new vaccine, and the Food and Drug Administration announced its approval on Tuesday for use in the US. Not only should you be weary of this vaccine due to negative history revolving around vaccines, but the fact that it is made with a genetically modified virus adds even more concern over its approval. While the researchers are delighted by the creation, individuals are being sought out for human trials - but you won't want to volunteer.

The researchers have been studying HIV and AIDS for 20 years and have spent the last 10 developing the vaccine. Starting in January, the vaccine will undergo three phases of human clinical trials.

Phase I - The first phase is meant to analyze the vaccine and determine if it is toxic in the human body.

Phase II - During phase two of the human clinical trials the researchers will look at the immune response to see if the vaccine actually performs like it is supposed to by inducing the proper immune response.

Phase III - In phase three 6,000 people are needed so that statistical data can be accumulated and later presented. For the testing, a vaccinated and non-vaccinated group will be compared to see if the vaccine protects against HIV infection or not.

Unfortunately, the researchers will likely be dismayed as nearly all vaccines are toxic to the body thanks to the rather large amount of heavy metals present in vaccines. We can see from the history of the flu vaccine as well as the gardasil vaccine that many problems can arise from vaccinations. To add to the potential dangers of this new vaccine, the fact that it contains a genetically modified virus simply can't be overlooked. The insurmountable evidence linking genetically modified substances with both the downfall of public health as well as the ruin of the environment shows that there is no room for extreme genetic modification in our lives. I know I certainly wouldn't volunteer to be a part of the experimental genetically modified-vaccine concoction.

Comment: Anything the FDA approves may kill you, as with GMOs, so know that these diseases are created mostly by man's interference that was part of the destruction of the homeopathic medicine that once existed and where anomalies such as cancer for profit did not rear their ugly heads. It all about profit now, nothing else.

Scientific History: Alan Watts on Bertrand Russell and Mind Programming

April 29, 2011: Alan Watt - The Impact of Science on Society 



More info on Bertrand Russell:
http://www.crossroad.to/Quotes/fascism/Bertrand%20Russell.htm
http://www.oldthinkernews.com/?p=848

The Scientific Outlook examined (Highly Recommended)
Part 1 - http://www.wiseupjournal.com/?p=375
Part 2 - http://www.wiseupjournal.com/?p=389
Part 3 - http://www.wiseupjournal.com/?p=405
Part 4 - http://www.wiseupjournal.com/?p=416
Part 5 - http://www.wiseupjournal.com/?p=437
Unable to find Part 6
Part 7 - http://www.wiseupjournal.com/?p=458
Part 8 - http://www.wiseupjournal.com/?p=473
Part 9 - http://www.wiseupjournal.com/?p=485

Read online or download "The Scientific Outlook (1954)" here:
http://www.archive.org/details/scientificoutloo030217mbp

Visit the website of Alan Watt here:
http://www.cuttingthroughthematrix.com/

Tuesday, December 20, 2011

Occupy Christmas (instructions)

Occupy the family holiday table? Incisive video survival guide! - Washington Blog

Occupy has all the facts that the 1% “leadership” in the US have committed massive crimes centering around war and money.

But how does one frame such an issue at the family holiday table?

This brilliant 6-minute video addresses this challenge!

Happy Holidays: may 2012 be your family and your best year yet, and may that be true for every new year.

Exposed: Genetically-modified salmon found to be contaminated with infectious salmon anemia

© greenberg-art.com
Exposed: Genetically-modified salmon found to be contaminated with infectious salmon anemia by Ethan A. Huff

 (NaturalNews) As the US federal government continues to evaluate whether or not to approve AquaBounty's genetically-modified (GM) "AquAdvantage" salmon, Canada's Cohen Commission (CC), a group established by the nation's government to track the decline of Sockeye salmon in the Fraser River, has announced some shocking information. According to a recent report, AquAdvantage being raised at a land-based, isolated site on Prince Edward Island have been found to be contaminated with Infectious Salmon Anemia (ISA), a serious viral disease that affects Atlantic salmon.

Catherine Stewart from the Living Oceans Society and Coastal Alliance for Aquaculture Reform recently gave an interview in which she explained the mysterious ISA discovery in the "Frankenfish." According to the CC report, Canada's Department of Fisheries and Oceans (DFO) reported to the Canadian Food Inspection Agency (CFIA) back in 2009 that there had been an outbreak of ISA at the Prince Edward Island facility raising AquAdvantage salmon.

"I think we have to ask the question, 'How did this get into this facility?' This is a land-based, closed-tank system that's raising these genetically-engineered fish," said Stewart. "It could only have come through the eggs or the smolts, or through water that the facility pumps from the bay into their facility."

AquaBounty is the same company, of course, that has been trying to ramrod US Food and Drug Administration (FDA) approval for its highly-allergenic AquAdvantage Frankenfish without so much as a shred of independent, legitimate scientific evidence proving that the imitation fish is safe for humans and the environment, or that it will not reproduce and destroy stocks of wild salmon all over the world (http://www.naturalnews.com/GM_salmo...).

Meanwhile, this Prince Edward Island scandal clearly illustrates that AquaBounty is incapable of even protecting its own protected stocks of fish from disease, let alone protect the world's oceans from contamination. If the company cannot even maintain its own disease-free, protected environment, how can it be trusted not to release GM fish and their traits into the wild?

"Was AquaBounty getting [its] eggs from Norway, Scotland, and were these ISA-infected eggs? We don't know," added Stewart. "And if [AquaBounty] had that disease in its facility, what's happening to the water they are dumping into the bay? What percentage of the water they use in this facility is recirculated, and what percentage goes out as effluent into the receiving waters, and does that effluent water contain the ISA virus? Are they treating the effluent? Again, we don't know."

Why Is the FDA Saying It's OK to Eat Seafood 10,000 Times Over the Safe Limit for Dangerous Carcinogens?

© n/a
Why Is the FDA Saying It's OK to Eat Seafood 10,000 Times Over the Safe Limit for Dangerous Carcinogens? by Brad Jacobson

 FDA not only downplayed the risk of contamination, but ignored staff members who proposed higher levels of contamination protection.

Ever since the largest offshore oil spill in history spewed into the Gulf of Mexico last year, independent public health experts have questioned the U.S. Food and Drug Administration's efforts to effectively protect Americans from consuming contaminated seafood.

Now a recent study by two of the most tenacious non-government scientists reveals that FDA Gulf seafood "safe levels" allowed 100 to 10,000 times more carcinogenic polycyclic aromatic hydrocarbons (PAHs) in seafood than what is safe. The overarching issue the report addresses is the failure of the FDA's risk assessment to protect those most vulnerable to the effects of these chemicals, such as young children, pregnant women and high-consumption seafood eaters.

In an effort to pinpoint how the FDA decided to set its acceptable levels for PAH contaminants in Gulf seafood, researchers at the Natural Resources Defense Council, which performed the study -- published in the leading peer-reviewed environmental health journal Environmental Health Perspectives -- also scoured documents wrested from the FDA under the Freedom of Information Act.

These include internal emails and unreleased assessments that suggest the FDA not only downplayed the risk of contamination but also that the EPA, and even members of FDA staff, had proposed higher levels of contamination protection, which in the end were ignored.

In vehemently denying the NRDC study's findings, the FDA argues that its chemical risk assessments are inherently biased "on the side of safety" and that setting higher protective health measures for PAHs in Gulf seafood would actually "do more harm than good."

Robert Dickey, director of the FDA's Gulf Coast Seafood Laboratory, who's taken the lead for the agency in responding to the NRDC report, elaborated in an email to AlterNet, "Overly conservative estimates would lead you [to] remove a great deal of food from our refrigerators and pantries than is needed."

In an interview with AlterNet, the study's lead researcher, NRDC staff scientist Miriam Rotkin-Ellman, said that such a response from the FDA "begs the question of whether or not it was a political versus a scientific decision" because the agency "does not provide scientific evidence" for the claim that being more health protective somehow carries an increased risk of doing harm.

She added, "PAHs in food have been evaluated and standards set in the European Union without jeopardizing anyone's nutrition."

AlterNet confirmed that the FDA indeed has provided no scientific evidence to back up this claim in either its formal response to the NRDC report or in addressing AlterNet's questions.

More broadly, the FDA declined to directly explain the email correspondence the study's researchers obtained in the FOIA request. They reveal that the Environmental Protection Agency, and even members of the FDA's own staff, questioned the FDA's seafood safety risk assessment criteria for protecting the most vulnerable populations, particularly Gulf residents.

Other documents received via the FOIA request show that the FDA considered multiple other potential calculations and criteria where more health protective risk assessments were considered but never followed.

Asked if these documents, along with the NRDC study's findings, belie the FDA's chief claim that their risk assessments are biased "on the side of safety," Dickey responded, "The seafood safety risk assessment was developed in extensive and open collaboration between FDA, EPA, CDC, NOAA, and public health experts and toxicologists from all five Gulf states impacted by the oil spill."

He added, "During that process many factors and calculations were considered before the final version was agreed on by all participants."

Dickey also claims that the FDA has "built into our assessments, a more than 100-fold safety factor that gives us confidence that sensitive populations are protected."

Yet Rotkin-Ellman countered that this conclusion is based on "outdated science" in which FDA calculations relied on the average lifetime weight of a 176-pound person.

"FDA continues to ignore the best scientific evidence on early-life vulnerability to chemical contaminants, which has shown that it is not sufficient to rely on life-time assessments," she said.

"The National Academy of Sciences and EPA guidelines emphasize that additional steps must be taken to specifically assess early-life stages," Rotkin-Ellman continued, "which includes calculating exposure based on age-specific bodyweights and adjusting to account for increased susceptibility."

The NRDC study found, for example, that the risk of cancer associated with eating Gulf shellfish contaminated at levels the FDA has deemed safe could be as high as 20,000 in a million. In other words, if 1,000 pregnant women consumed Gulf seafood at these levels, 20 of the children they give birth to would be at significant risk of cancer from the contamination.

The report also concluded that based on available testing data on PAH levels in shellfish after the spill, up to 53 percent of the shrimp tested had PAH levels exceeding the NRDC researchers' revised levels of concern for pregnant women who are high consumers of Gulf shellfish.

In the interview with Rotkin-Ellman, she highlighted many other central weaknesses in the FDA's protective criteria for PAHs in Gulf seafood about which she and her NRDC study co-author and UCSF clinical professor of health sciences, Gina Solomon, have long been concerned. These include underestimating the amount of seafood Gulf residents consume, ignoring cancer risk from naphthalene contamination (one of the most prevalent PAHs in petroleum) and projecting the contamination will only last five years.

Another key finding the NRDC report confirmed is that the FDA has no set levels of acceptable PAHs in seafood, but rather creates them on a case-by-case basis after each oil spill.

For example, the FDA made PAH "safe levels" less stringent after the BP oil spill than they had been following the Exxon-Valdez spill.

Asked to explain this practice, Dickey replied, "Each oil spill can involve different kinds of crude oils or refined oil products in different types of environments, so the responses are different to account for the physical environment and the compounds of concern that must be tested for."

He added, "Also, over time scientific knowledge of the toxicity of the many hundreds to thousands of compounds in oil and refined oil products increases, which directly affects the analysis of risks involved."

But Rotkin-Ellman noted his answer simply evades the underlying question.

"There are core PAHs of public health concern that are present in most petroleum products that FDA could set standards for regardless of the specifics of an oil spill," she said. "If analyses prove that those PAHs are not present in the next oil spill then those standards will not be applicable."

But this variability, she went on to say, does not preclude FDA from evaluating health threats from PAHs now.

"The ad-hoc risk assessment performed by FDA without public or outside expert review," Rotkin-Ellman added, "have jeopardized FDA's credibility and they have lost public confidence."

Currently, the FDA has no plans to begin setting standard levels of concern for PAHs in U.S. seafood, as Europe does to protect its citizens. The NRDC recently filed a petition with the FDA to change this practice but has yet to receive a response.

Gulf seafood continues to be tested on a limited basis. On the FDA's Web site, the agency contends that seafood from the Gulf "is as safe to eat as it was before the oil spill."

Monday, December 19, 2011

Top 10 Most Important Health Freedom Stories of 2011

© arapaho.nsuok.edu
Top 10 Most Important Health Freedom Stories of 2011 by Anthony Gucciardi

2011 was an amazing year for the health freedom movement, with monumental victories against Monsanto, Merck and money-hungry pharmaceutical corporations as a whole.

As the year comes to a close, it is important to look back on some of the most important stories that helped to propel the natural health movement into the mainstream spotlight.

More than just listing the articles, you will receive an inside look into each story - from the true importance and depth of the story to the reciprocation and possible spin by the mainstream media.

1. Monsanto Declared Worst Company of 2011

The impact of this story is not solely based on the profound anti-Monsanto content that it holds. Instead, the real importance of this story - and the fact that it is the #1 most important story of 2011 - is due to the fact that it was carried by Reuters, Yahoo News, and thousands of other major publications. It was seen by millions browsing the news, searching Google, and seeing the latest Twitter, Facebook, and Youtube posts on the subject. Yahoo News alone receives 74 million visitors on average each day. This article, published to the mainstream media in the form of a press release, brought Monsanto's assault against the environment and public health to the spotlight of the masses.

Monsanto was certainly not happy to see this controversial article go up on top publications and rack up around 198,000 results on Google alone.

2. Pharmaceutical Drug Deaths Now Outnumber Traffic Fatalities in US

Killing at least 37,485 people nationwide, pharmaceutical drug deaths now exceed traffic-related fatalities according to statistics from the U.S. Centers for Disease Control and Prevention. This information is shocking at face value, but it is even more explosive when you examine the depth of the subject. In fact, pharmaceuticals are actually breeding illness... then more pharmaceuticals are prescribed to 'treat' the generated illness. These pharmaceuticals then lead to further harm, and this cycle continues for the entire life of many individuals stuck in this paradigm.

Antibiotics are causing a diminished immune system through permanently depleting gut flora, creating obesity, mental illness, and much more. Antidepressants are actually leading to more suicidal thoughts and depression. Is it any wonder pharmaceuticals are killing more people than traffic accidents?

3. Hungary Destroys All Monsanto GMO Corn Fields

Generating over 220,000 shares, making it the 10th most shared article of 2011, this explosive report has made waves around the Internet that have outdone mainstream outlets such as Huffington Post and CNN. Complimenting the success of Monsanto's Worst Company of 2011 Award, the article reached hundreds of thousands of readers and highlighted the powerful resistance to Monsanto that is being seen worldwide. The huge amount of shares that this article generated has also allowed for even mainstream media readers to get a glimpse of the truth, with this anti-Monsanto article informing and empowering readers across the globe.

Looking back, this article will be a major part of the anti-Monsanto revolution that helped bring awareness and support to the cause.

4. Government Ignored 1998 Report Finding up to 100 Cancer Deaths from TSA Naked Body Scanners Per Year

The TSA has been asserting the safety and usefulness of their privacy-invading X-ray scanners in the face of public outrage for far too long. The TSA, and the United States government as a whole, actually knew in 1998 that these scanners were giving you cancer, yet they were still approved to be used in airports across the nation! Keep in mind that the 100 annual deaths estimated by the radiation experts in the report are not only conservative, but they were based on the experimental X-ray scanners that actually had somewhat regulated radiation output.

Current scanners have been found to put out 10 times the radiation they are supposed to, frying you with radiation in order to invade your privacy. This article is the 4th most important, as it is all that is truly needed to put an end to TSA naked body scanners. It shows that the government blatantly ignored the warnings of renown radiation experts, deploying these DNA-damaging scanners with zero concern for public health.

5. Flu Shot Found to be Ineffective, Dangerous - The Flu Shot Timeline

In 2011, more vital information regarding the flu shot surfaced than ever before. Linked to narcolepsy, deadly nerve disease, and even found to be ineffective at reducing the flu, 2011 spelled the informational end of the flu shot. In addition, it was even found that inexpensive and safe vitamin D can slash your risk of the flu far more effectively and without side effects by nearly half. Amazingly, this was with severely low vitamin D dosage, and with optimal levels that flu reduction percentage would surely increase.

This article compiles all of the recent evidence on the flu vaccine, running down the list of scientific research in a compact yet powerful delivery. Why is it the 5th most important article? The flu vaccine has been heavily pushed on everyone from toddlers to seniors for years by government institutions, putting public health at risk and propagating the false myth of its safety and effectiveness. The information compiled in this post refutes the blind push to receive the flu shot, and its circulation could end the very routine.

6. BPA Can Make You Infertile

Bisphenol A has become a mainstream issue, and for good reason. This is due to the fact that activists and readers like you have forced the mainstream media to cover the topic, though very few publications truly discuss the real depth of the BPA issue. That's why the 6th most important article explains just how devastating BPA is to your health. In fact, it is so devastating that it threatens the reproductive abilities of humankind.

BPA can be found in most plastics, cans, baby bottles, and much more. 2011 was the year of BPA awareness, and hopefully 2012 will be the year of BPA abolition.

7. Nations Under 'GAVI Alliance' UN, Bill Gates Foundation Push Deadly HPV Shots on Poor Nations Under 'GAVI Alliance'

While this story could easily be included in the top 3, the true effects of the GAVI Alliance's initiative will not be felt until it is rolled out onto unsuspecting poor nations. In this story, exclusive to NaturalSociety (though copied without credit by many other publications), I expose the GAVI Alliance as an organization funded by organizations such as the World Bank, The Bill & Melinda Gates Foundation, the vaccine industry, UNICEF, and many other rogue philanthropists. Led by these investors, the GAVI Alliance seeks to vaccinate the residents of third-world nations with the HPV shot, most likely under the brand name Gardasil.

Between May 2009 and September 2010 alone, Gardasil was linked to 3,589 harmful reactions and 16 deaths. Of the 3,589 adverse reactions, many were debilitating. Permanent disability was the result of 213 cases; 25 resulted in the diagnosis of Guillain-Barre Syndrome; and there were 789 other "serious" reports according to FDA documents. Why would any organization truly dedicated to helping poor nations choose to vaccinate children with the Gardasil vaccine? This story is essential, as it exposes this initiative before it takes place. After the campaign occurs, there will surely be many reports of death and adverse reaction from the trusting third-world residents.

8. Merck Pays $950 Million in Criminal Fines and for Falsely Marketing Vioxx

Merck is not only the maker of death-linked Gardasil, but also the manufacturer of Vioxx - the drug that they falsely marketed to consumers despite links to over 27,000 heart attacks and sudden cardiac death. In a monumental case, the company was issued to pay $950 million with $321.6 million in criminal fines, while the remaining $628.4 million was put toward a civil settlement agreement. While this is only a dent in the massive financial prowess of the company, the fine was a groundbreaking step in the fight against the corruption of the pharmaceutical industry.

9. Legislation Launched to Label GMOs

Two new bills have been introduced by representative Dennis Kucinich that are aiming to not only mandate labeling of genetically modified foods, but also to bring in a new set of rules to make GMOs safer. One of the bills known as The Genetically Engineered Food Right to Know Act was introduced on December 2, 2001, and has 12 co-sponsors and bipartisan support. Whether or not both bills become law, the initiative is of extreme importance and is a byproduct of the growing anti-GMO movement that 2011 has encompassed. If these bills pass in or before 2012, it will easily be one of the most important stories of the decade.

10. Monsanto's Carcinogenic Roundup Herbicide Contaminating Water Supply

New research has confirmed what myself and other health-conscious individuals have been saying about Monsanto's best-selling herbicide Roundup - the carcinogenic chemical it contains known as glyphosate has been found to be contaminating the groundwater in areas where it is being applied. What does this mean? It means that toxic glyphosate is now polluting the world's drinking water through the widespread contamination of aquifers, wells and springs. This is only the beginning of the findings that will ultimately bring the true dangers of Roundup to light in 2012 and beyond.

Visit Natural Society for more great health news and vaccine information.