A Natural Environmental Health Facts Ezine
 Information For Getting Healthy

Lena Sanchez Editor


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"A NATURAL ENVIRONMENTAL HEALTH FACTS Ezine"  Here to Inform and Help You Become Healthier and Happier while Achieving Quality Longevity!

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=> IN THIS ISSUE!
============================


==> Editors' Ranting & or Warnings
==> Something To Think About
==> Health Thought for the day!
==> Showcase Health Spotlight
==> Monthly Spotlight Ads
==> Today's Health Tip
==> Food of The Week (Sunday only)
==> Health Today
==> Environmental Report
==> Life Changing Information



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EDITORS' RANTING
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Greetings and thank you for being an optin subscriber!

The storms continue to pelt us with lightening strikes and some rain and I prepare to take a vacation from all of it. Well, I may be going into Oklahoma tornado country so I might not actually escape bad weather! I will be away from the office and work until 9/12 so if you need to reorder or order formulas be sure to get them to me by Tuesday no later than 9PM!  I will have no internet access for a few days and possibly the whole time I'm gone... Cell phone only and hopefully that won't be intermittent as some of those Oklahoma hills have no cell service... 928-713-3624

A Natural Environmental Health Facts will be published next on 9/13/2006...

The answer will publish in Tomorrow's "Ask Lena Health Q & A" But we like to give a more personal answer to the writer, so please resend that email...

Take charge of you and your family's health before it takes charge of you!
Lena

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Something To Think About
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FDA APPROVES VIRAL ADULTERATION OF OUR FOOD SUPPLY
By Byron J. Richards, CCN
August 24, 2006

On Friday, August 18, 2006, the FDA approved a viral cocktail to be sprayed on foods we eat. This is the first time viruses have been approved for use as food additives. The FDA wants you to believe it will be safe to consume these viruses every day for the rest of your life with no adverse health effects. Not surprisingly, the FDA doesn't want you to know which foods are adulterated in this manner, for fear you may not buy them; thus, no labeling will be required. This is a monumental announcement by the FDA, indicating they are throwing all caution to the wind regarding the safety of our food supply.

Are you willing to stand in line for a virus-laden sandwich? How do you like the idea of buying virus-infested food for your family? The first virally contaminated foods entering our food supply with the blessings of the FDA will be luncheon meat and poultry. Live viruses will be sprayed on foods such as cold cuts, sausages, hot dogs, sliced turkey, and chicken.

At issue is the very real problem of a poor quality FDA-approved food supply that is already full of diseased and sickly animals, many of them imported from other countries. The use of antibiotics during growth and radiation during food processing is required by the fast-food animal farms owned by multi-national companies to cover up the horrendous health of the animals they wish to feed to Americans. Animals in poor health are a friendly place for bacteria to grow and prosper, especially after such meat goes to market. Rather than address the source of the problem, the FDA wants to add another adulteration into our food supply.

The stated goal of the new FDA-approved viruses is to kill a rare bacterium known as Listeria monocytogenes. This bacterium is killed by cooking; however, it poses a problem in meats that are cooked during processing and not cooked again prior to consumption, so it can readily infect foods such as deli meats.

Yes, the FDA plans to use one infectious organism to fight another. The carnage of battle will end up in your digestive tract along with the victorious live viruses, which the FDA assures us will not attack human cells. However, they cannot possibly be certain the viruses will not attack the friendly bacteria that make up the lining of your digestive tract. And they want you to believe this is completely safe while refusing to require the additive viruses to be listed on the food label so that you would have a choice.

Turning Loose the Bacteria-Killing Viruses

The company that produces these biotech viruses is Baltimore-based Intralytix, Inc. The viruses are known as bacteriophages, viruses that kill bacteria, or phages for short. Phages have been around a long time, living as parasites inside many bacteria.

Intralytix uses biotechnology to grow viral phages in a culture with Listeria, in theory teaching the viruses to recognize the bacteria. The FDA-approved cocktail contains six different viruses intended to attack one strain of bacteria.

This concoction is then sprayed on food. If Listeria is present in the food, the bacteria will ingest the viruses. This results in massive viral replication inside the bacteria, until such point as the bacteria simply bursts. This battle results in significant production of bacterial poisons called "endotoxins", as the bacteria tries to defend itself. When the bacteria burst, these endotoxins are released. These, along with the victorious live viruses, will now be on the food that will be eaten.

The FDA and Intralytix would like us to believe that these viruses will only attack the specified bacteria they are intended to kill and will be harmless to humans. I'm sorry to burst their bubble, but they can't possibly guarantee such safety. It is true that the viruses, at least at this time, cannot recognize human cells. However, the virus can potentially recognize normal bacterial cells in the human digestive tract and may be able to adapt to infect one or more of these friendly bacteria.

The FDA Certainly Knows There Are Risks

The FDA had some concerns about the amount of bacterial endotoxin in the Intralytix product before it is sprayed; however, FDA tests apparently showed that the product was adequately purified and so they declared it safe if used as approved. Will the FDA diligently monitor the quality of this product once it is on the market, or will it go the path of many FDA-approved drugs that the agency can't keep track of?

There is certainly a risk that humans will be exposed to excessive amounts of endotoxin. This could come from the manufacturing of the viral cocktail, the interaction of the viruses with bacteria after being sprayed on food, and/or the interaction of the viruses with bacteria in the digestive tract.

The human immune system is highly reactive and sensitive to bacterial endotoxins. They provoke allergy, asthma, autoimmune problems, and elevate cholesterol. They also interfere with the healthy function of cells lining the digestive tract. Researchers have demonstrated that the presence of bacterial endotoxins can start cancer in the colon.

Additionally, the human immune system reacts directly to viral phages. Thus, a person who eats a lot of processed deli meat is certain to evoke an immune reaction to the viruses. What will this reaction be? Allergy? Asthma? Autoimmunity? Cancer? How can the FDA approve a food additive that it knows can induce a variety of human immune responses? Phages are so good at disrupting normal immunity that they are being considered for use as part of organ transplant medicine.

The ingestion of significant amounts of viral phages into the human digestive tract is a wild card full of unknown outcomes. For example, it is certainly possible that these phages, which constantly mutate in order to survive, are likely to find a way to infect bacteria they were not intended to infect. Since phages are parasites, they could hijack the friendly bacteria of the digestive tract and turn them into viral machines, constantly generating viral particles that are likely to confuse the human immune system, if not directly infect the body. We know from history that these viral phages can turn innocuous bacteria into a killer, which is how cholera occurs.

Furthermore, the Listeria bacteria are not going to take the issue lying down. They will develop resistance to the viruses over time, as we have seen with the overuse of antibiotics. Going down this path we are likely to have hundreds of viral food additives in the food we eat, all designed to combat some possible infection coming from poor quality food. Sooner or later we will inadvertently create deadly new super-strains of bacteria and/or parasitically infect the human digestive tract with an untreatable infection.

There is also the very real possibility of unintended viral recombination. What happens when a person with viral stomach flu eats food containing a dose of this viral food additive? It is certainly possible for the genetic material of the flu virus to interact with the genetic material of the viral phages, provoking an undesirable new viral infection.

Let's not forget that the FDA won't tell us which foods in the food supply contain genetically modified organisms (GMO). Seventy percent of the packaged food on grocery shelves already contains GMO adulterated food. These foods have viral promoter genes woven into the DNA of every cell, a technique used to implant a pesticide toxin into every cell of this fake food (see Fight for Your Health, chapter 15). What happens when the viral phages interact with the viral promoter genes in GMO food? What new virus will be encouraged to form?

Keep in mind that the FDA wants to conduct this experiment on our food supply to protect a small minority, only about 2500 people, who are made seriously ill by this infection each year. The ill are mostly pregnant women, elderly with compromised immunity, and small children. It would be a lot more to the point if the FDA would simply warn such people that eating these foods, due to their poor quality of production, may be dangerous. What the FDA should really do is improve the quality of our food supply, the true source of the problem. Why expose millions of Americans to an unproven ingestion of live viruses for the benefit of so few?

The FDA has failed miserably for the past century to protect the public from the adulteration of our food supply by vested interests. This is just one more insult added to a long list of injuries.

The Tip of an Iceberg

Intralytix has an agenda for the American food supply, as well as for healthcare in general. This recent FDA ruling allows Intralytix and other similar biotech companies to get their foot in a door that should be slammed shut and bolted closed.

The company is also seeking FDA approval for viral sprays to treat foods that could be contaminated with E. coli and Salmonella, which means that similar "trained" viruses could end up in a majority of the protein foods in our food supply.

Intralytix sees financial opportunity. They have already licensed their now FDA-approved viral spray to an undisclosed multi-national company for use around the world. When the CEO of Intralytix, John Vazzara, was recently asked about this partner company, he refused to disclose their name. The grand profit-driven biotech experiment on the health and well being of all Americans is now in full swing.

Of course, we will need new wonder drugs to combat the new bio-tech produced infections. Americans will stay sick and the sickness-driven bio-tech industry will flourish. The bio-tech industry will make people sick on the front end and treat them on the back end. It's a win-win situation for profit on illness.

The FDA is Rapidly Becoming a Public Enemy

Experimenting with viruses being added to the food supply is incredibly dangerous and reckless.

Read the rest of the story Click Here


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THOUGHT FOR THE DAY!
=======================


"NINE REQUISITES FOR CONTENTED LIVING:


**Health enough to make work a pleasure.
**Work enough to support your needs.
**Strength to battle with difficulties and overcome them.
**Grace enough to confess your sins and forsake them.
**Patience enough to toil until some good is accomplished.
**Charity enough to see some good in your neighbor.
**Love enough to move you to be useful and helpful to others.
**Faith enough to make real the things of God.
**Hope enough to remove all anxious fears concerning the future."

~Johann von Goethe


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Of all the physical changes that occur with age, the most apparent are the changes in your skin. You may eventually feel the cartilage in your joints wearing thin, but wrinkles and lines stare back at you every time you look in the mirror.

Your skin really started aging decades ago

The aging process started taking its toll on your skin in your thirties as the oil glands began decreasing their output, making your skin drier. During your forties production of collagen and elastin (proteins that give skin tissue its structure and elasticity) declined, and wrinkles and sags probably became more noticeable. And after the age of 50, all of these mechanisms gather speed-sometimes at an alarming pace.

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 TODAY'S HEALTH TIP

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Drug linked to cataract surgery problems
Tue Aug 22, 2006
 
WASHINGTON - Patients taking a widely prescribed prostate drug should alert their eye doctors before undergoing cataract surgery to avoid complications, several medical groups said Tuesday.

Advance warning can allow surgeons to modify their technique during the common operation and avoid complications seen in patients who take Flomax and similar drugs to treat enlargement of the prostate, the groups said.

The drugs, called alpha-blockers, appear to impair a muscle in the iris, the colored portion of the eye. The iris must be stimulated during surgery to replace the clouded lens of the eye to allow the opening in its center, the pupil, to dilate. The drugs seem to cause the iris to unexpectedly flap or billow.

Any unexpected movement during surgery can cause injuries to the iris and other complications, said Dr. David F. Chang, a clinical professor of ophthalmology at the University of California, San Francisco and a spokesman for the American Academy of Ophthalmology.

Surgeons can use tiny hooks to keep the pupil open or administer stronger dilating medicines directly inside the eye to accommodate the problem, called intraoperative floppy iris syndrome, Chang said.

Preliminary results from a recent study suggest there are no more complications following modified surgery on patients taking Flomax compared to operations on patients who don't take Flomax or similar drugs. The drugs typically are taken by men, although they are prescribed to some women for urinary retention.

Patients considering cataract surgery do not need to stop taking the drugs, the American Academy of Ophthalmology, the American Society of Cataract and Refractive Surgery and the American Urological Association said in a joint warning.

The drugs' labels, approved by the Food and Drug Administration, already mention the potential complications.

 


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FOOD OF THE WEEK
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Yellow, Red, White, Blue (Zea mays var. rugosa)

 Today's vegetable come in an array of colors such as yellow, red, white and blue with variations in between of all those… And sadly I received some really bad information in my early adult years on this vegetable. A badly informed friend told me that today's vegetable had no nutrients in it to help us and that it was a wasted food… How that rumor got started I will never know but it is absolutely false! I did not take the time to even look it up then but I have since found that is absolutely a far fetched fallacy!

 Corn season is here in our area and the annual Community Corn Dinner is held every year and this year is no different…

 Our veggie this week, corn contains a multitude of nutrients… Fiber to keep our bowels regular and healthy, along with a multitude of Minerals such as; Calcium, Iron, Magnesium, Phosphorus, Potassium, Sodium, Zinc, Copper, Manganese and Selenium. And many Vitamins such as; Vitamins A, C, B-6, B-12, E, Thiamin, Riboflavin, Niacin, Pantothenic acid, Folate and Folic acid.

History and Origin

 In Native American usage, the word for corn means "our life," or "our mother," or "she who sustains us." It was the cultivation of corn that turned Native American tribes from nomadic to agrarian communities.

It was from the Native Americans that the first European settlers learned about corn. Native Americans had spent hundreds of years developing what we now know as corn from seed-bearing grass. Long before Christopher Columbus sailed from Spain in 1492, Native Americans were cultivating this grass in North, Central, and South America. Native American farmers in the Ohio River Valley had been growing corn for more than 1,700 years before the first white men crossed the Appalachian Mountains, and there is evidence that they used corn to brew beer before Europeans arrived in the Americas.

 The Pawtuxet Indian tribe in Massachusetts was cultivating corn when the first settler arrived, and corn was on the first Thanksgiving table in 1621. If it had not been for corn, the Pilgrims of Plymouth Colony might have starved to death during their first year in America. The Indians taught settlers how to grown corn, pound corn into meal, and how to cook with it. The words of Governor William Bradford, first governor of the Plymouth Colony, now inscribed on a brass plaque at Truto (Corn Hill) on Cape Cod, Massachusetts, reflect the settler's gratitude: "And sure it was God's good providence that we found this corn for we know not how else we should have done."

 At first, when taken into Europe, corn was only a garden curiosity but it soon began to be recognized as a valuable food crop. Within a few years, it spread throughout France, Italy, and all of southeastern Europe and northern Africa. By 1575, it was making its way into western China, and had become important in the Philippines and the East Indies.

 Although corn is indigenous to the western hemisphere, its exact birthplace is far less certain. Archeological evidence of corn's early presence in the western hemisphere was identified from corn pollen grain considered to be 80,000 years old obtained from drill cores 200 feet below Mexico City. Another archeological study of the bat caves in New Mexico revealed corncobs that were 5,600 years old by radiocarbon determination. Most historians believe corn was domesticated in the Tehuacan Valley of Mexico. The original wild form has long been extinct.

 Cooking sweet corn, whether you cream it, steam it or keep it on the cob, unleashes beneficial nutrients that can substantially reduce the chance of heart disease and cancer, according to Cornell University food scientists. The study found that cooked sweet corn retains its antioxidant activity, despite the loss of some vitamin C.

 The word "corn" has many different meanings depending on what country you are in. Corn in the United States is also called maize or Indian corn. In some countries, corn means the leading crop grown in a certain district. Corn in England means wheat; in Scotland and Ireland, it refers to oats. Corn mentioned in the Bible is said to probably refer to wheat or barley. Of course I didn't live then nor do I know anyone who did and cannot verify that…

 Our favorite way of eating corn is grilled in its husk. I usually pull the husk back, remove as much of the silk as possible and make sure it's worm free, then pull the husk back over the cob and put on a BBQ grill, medium flame, and cook until husk is well burned… Turning frequently to cook evenly… Then butter and eat. We also like it raw on the cob, when it is fresh off the stalk… We also steam it and eat… I do not put a lot of seasoning on it as we like the flavor natural…But corn can be fixed many different ways. Corn can be found frozen through out the year so you can enjoy this nutritious food any time…

The grandchildren are quick to ask for and love our Summer Sabbath suppers of Popcorn and mixed fresh fruit salad, occasionally, when they are here…  Corn is great any way it's fixed to eat…

Enjoy this nutritious food,
Lena


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HEALTH TODAY
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The Latest Killer Statin Scam: Preventing Strokes
 
A new study supports the use of cholesterol-lowering statin medications to help prevent the recurrence of a stroke. The drugs seemed to help even those with no prior history of heart disease. The study was funded by Pfizer, the drug company that makes Lipitor.

Reduced Risk

Researchers looked at more than 4,700 people, none with a history of coronary disease, who had suffered from strokes or transient ischemic attacks, a ministroke caused by the temporary blockage of a brain artery. Patients who took Lipitor after a stroke had their risk of a second stroke reduced by 16 percent over five years.

Same Death Rate

However, there was no difference in the overall death rate between those who took statins following their stroke and those who did not. There was also a slight increase in stroke risk among patients who took statins following a rarer kind of stroke caused by a leaking blood vessel.

 
New England Journal of Medicine  August 10, 2006; 355(6): 549-559
 

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    ENVIRONMENTAL REPORT      
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Judge Strikes Down Pesticide Usage Rule
Aug 25, 12:25 AM (ET)2006
By GENE JOHNSON

SEATTLE (AP) - A federal judge on Thursday rejected a Bush administration decision to weaken rules governing pesticide use, saying the change lacked scientific justification.

It was the second time in recent years that U.S. District Judge John C. Coughenour chastised federal agencies for failing to follow the Endangered Species Act in licensing pesticides for sale.

In 2001, environmental groups sued over the Environmental Protection Agency's failure to consult with the National Marine Fisheries Service or the U.S. Fish and Wildlife Service before allowing certain pesticides to be sold. Coughenour ordered the EPA to conduct the consultations in determining whether 55 of the pesticides were likely to harm salmon.

Instead, in 2004, the administration created a new rule allowing it to ignore the consultation requirement of the Endangered Species Act. Officials reasoned the EPA should decide on its own whether pesticides were likely to harm protected species.
 
The environmental groups sued again, and on Thursday, Coughenour threw out the new rule, saying the government could not simply ignore the act's requirements.

"The administrative record is striking in its total lack of any evidence of technical or scientific support for the policy positions ultimately adopted," Coughenour wrote.

He noted that in 2004 the EPA asked fisheries service scientists to support its findings that 28 pesticides were not likely to harm protected species.

The agency's Washington state office did not agree in any of the 28 cases, according to an internal fisheries service letter. Nevertheless, that agency and Fish and Wildlife agreed to the rules change "knowing of the substantial flaws in EPA's methodologies," the judge said.

The EPA did not immediately return calls seeking comment Thursday, and spokesmen for the Fish and Wildlife Service and the National Marine Fisheries Service said they had not had time to review the ruling.

Earthjustice lawyer Jan Hasselman, who represented the Washington Toxics Coalition and other environmental groups in the lawsuit, said the EPA should be working with agency scientists to determine the safety of the pesticides for endangered species around the country.

"Instead of addressing that in a serious way, they've been looking for shortcuts," he said.

 

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