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A NATURAL ENVIRONMENTAL HEALTH FACTS free Ezine aka newsletter  Here to Inform and Help You Become Healthier and Happier while Achieving Quality of life longevity! The sometimes controversial healthy alternatives versus traditional medicine also pro's and con's of both. Covering all health topics.
If you received the publish notice forwarded by a friend or family member you can get your own notice for each edition simply Click To Subscribe by email


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Email Lena

928-636-9425
Wednesday  October 3, 2007
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Watch for Monday's "Ask Lena Health Q & A edition.
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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
==> 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!

Cool autumn weather is such a relief yet I know that a lot of illness is just around the corner because people procrastinate on illness prevention and wait until illness hits then wish they had done something different. Human nature in the majority. Don't be caught unaware get your immune system in gear to bounce illness off your body. Need to know how, ask and we will get that info to you ASAP!

Question or comment (good or not so good) Click Here 
Lena

ANEH Facts archives  Click Here 
Ask Lena Health Q & A Archives  Click Here
Your Home Business Coach Archives Click Here


TidBits Of Info

==> Find An Alternative Health Professional 
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Something To Think About
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FDA Continues Pushing Natural Herb Sweetener Stevia Out of U.S.
September 19, 2007


Hain Celestial Group Inc., the maker of Celestial Seasonings teas, received a warning from U.S. regulators that some of its powdered drink mixes contain an unsafe herb.

Some Celestial Seasonings tea mixes, called Zingers to Go, contain a South American herb, stevia, that must be removed from the products, the Food and Drug Administration said in a warning letter posted Tuesday on its Web site.

Stevia is a main staple sweetener in many countries, including Japan and China, where it's found in multiple food products. Companies including Coca-Cola Co. and Cargill Inc. have been developing products that substitute stevia for artifical sweeteners like aspartame, but the FDA currently bans any food product from containing the natural sweetener.

''While FDA has received inquiries and petitions for the use of stevia or stevia extracts in food, data and information necessary to support the safe use have been lacking,'' according to the FDA letter. But on the FDA's own website, a GRAS petition submitted to FDA in 1995 cited over 900 Stevia studies, none of which indicated any safety concerns regarding human health.

According to the American Herbal Products Association, "Stevia leaf is a natural product that has been used for at least 400 years as a food product, principally as a sweetener or other flavoring agent. None of this common usage in foods has indicated any evidence of a safety problem. There are no reports of any government agency in any of the above countries indicating any public health concern whatsoever in connection with the use of stevia in foods."

The agency's letter named the company's Zingers to Go Tangerine Orange Wave Herb Tea as containing the additive. Other flavors of the Zingers to Go powdered drink mix also were labeled on the company's Web site as containing stevia, according to the letter.

Stevia Quotes
"The petition cites over 120 articles about stevia written before 1958, and over 900 articles published to date. In this well-chronicled history of stevia, no author has ever reported any adverse human health consequences associated with consumption of stevia leaf."

Supplement to GRAS affirmation petition no. 4G0406, submitted by the Thomas J. Lipton Company February 3, 1995
"According to the Herb Research Foundation, numerous scientists, and tens of millions of consumers throughout the world, especially in Japan, the herb is safe and intensely sweet, which could make it a popular noncaloric sweetener."

Rob McCaleb, president, Herb Research Foundation, Boulder, Colo., USA
"...as a scientist with over 15 years researching the safety of stevia and of many other plants used as food or food ingredients, I can assure that our conclusions in these various studies indicate that stevia is safe for human consumption as per intended usage, that is, as a sweetener."

Mauro Alvarez, Ph.D., Brazil
"Stevia leaf is a natural product that has been used for at least 400 years as a food product, principally as a sweetener or other flavoring agent. None of this common usage in foods has indicated any evidence of a safety problem. There are no reports of any government agency in any of the above countries indicating any public health concern whatsoever in connection with the use of stevia in foods."

Gras affirmation petition submitted on behalf of the American Herbal Products Association, April 23, 1992
"...various extract forms of stevia have been extensively studied and tested. These tests include acute, sub-acute, carcinogenic evaluation and mutagenicity studies. These scientific data, while not directly relevant or required for exemption under the common use in food proviso, nevertheless demonstrate cumulatively that there is no safety problem associated with the use of an extract of stevia. It appear to be extraordinarily safe."

Introduction to GRAS affirmation petition submitted by the American Herbal Products Association, April 23, 1992
"(The FDA action on stevia is) a restraint of trade to benefit the artificial sweetener industry."

Jon Kyl (R), AZ in a 1993 letter to former FDA Commissioner David Kessler about the 1991 stevia "import alert."
"Stevia has a political problem."

Rob McCaleb, president Herb Research Foundation
"I had one guy from the FDA tell me 'if we wanted to make carrots (be) against the law, we could do it.'"

Kerry Nielson, former director of operations at Sunrider International, discussing the 1985 FDA seizure of his company's stevia.
"Even if they have reviewed these studies, the only possible way to report that the results showed detrimental effects is by taking information out of context. If this is the case, one concludes that these FDA scientists are incompetent and irresponsible, or if not, they must belong to some sort of conspiracy group to carry on a sinister agenda against this plant with the objective to keep it away from American consumers by attributing to it safety issues that do not exist."


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

When researchers studied the health records of 2,205 of brittle bone fractures over a period of 35 years, they found a direct relationship between the level of activity and the number of fractures (higher activity equaled fewer fractures). This was especially true of hip fractures. In fact, sedentary men were one and a half times more likely to suffer from a broken bone in general, and two and a half times more likely to suffer from a broken hip, specifically.


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We accept all advertisements in good faith, but the advertisers are completely responsible for the content and accuracy of their advertisements. We do not give any warranties and accept no responsibility. The editor and publisher suggest that you exercise due diligence! 
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 TODAY'S HEALTH TIP

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WHITEN YOUR TEETH WITH A HEALTHY WHITENER!

A safer alternative to brighten your teeth!

You can try this simple inexpensive trick:
Crush one ripe strawberry and mix it with 1/2 teaspoon of baking soda.
Spread the mixture onto your teeth and leave on for five minutes.
Brush your teeth with a little toothpaste (non-fluoride, of course) and rinse.


This natural mixture works because of the malic acid it contains, which acts as an astringent to remove some of the surface discoloration on your teeth. Though this method is perfectly safe to use on occasion, don't use it too often (no more than once a week) because the acid could potentially damage your tooth enamel with excessive use.

 


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 HEALTH TODAY
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Drug Trials Go Unwatched, Study Says
Sep 28, 2007

WASHINGTON (AP) - Clinical trials that enroll millions of patients in tests of experimental drugs and medical devices get scant government oversight, according to a watchdog report released Friday.

Over a six-year period, the Food and Drug Administration inspected just one of every 100 trial sites, raising questions about the agency's ability to ensure the safety of study participants, according to the report by Health and Human Services Department inspector general Daniel Levinson.

Hampered by the lack of a comprehensive catalog of clinical trials, the FDA is unable to even identify all trials, the estimated 350,000 study sites and the institutional review boards that oversee each study to ensure they meet scientific, ethical and legal obligations, the report says.

The FDA relies on just 200 inspectors to police human studies of drugs and devices. The inspections they perform focus more on ensuring the accuracy of trial data than on verifying the measures put in place to protect the study participants, the investigation found.

Even when inspectors do turn up serious problems, their findings are frequently downgraded by senior officials and almost never followed by inspections to see whether the issues have been resolved, according to the report. In the case of the FDA's drug office, 68 percent of inspector recommendations that the agency take regulatory action, typically in the form of a warning letter, were downgraded.

The FDA found serious problems at test sites 348 times between 2000 and 2005. But only 26 investigators were disqualified from conducting further clinical trials, and data were disqualified just twice, according to the report.

The FDA told the inspector general that inspections make up only one part of its efforts to ensure human subject are protected. The agency sees its review of study protocols before they get under way as the most important step in protecting participants.

The FDA oversees the safety of companies' drug or medical device trials, while the Office for Human Research Protections does the same for federally financed tests. There is no federal monitoring of privately financed, noncommercial trials.

In a report due to be released Friday, the inspector general of the Department of Health and Human Services, Daniel R. Levinson, said federal health officials did not know how many clinical trials were being conducted, audited fewer than 1 percent of the testing sites and, on the rare occasions when inspectors did appear, generally showed up long after the tests had been completed.


New York Time Article


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    ENVIRONMENTAL REPORT      
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U.S. Delays Approval of Farm Pesticide
Sep 28, 2007
By RITA BEAMISH

WASHINGTON (AP) - The Environmental Protection Agency on Friday delayed approval of a new toxic fumigant for use by fruit and vegetable farmers, after more than 50 prominent scientists objected that the chemical was too dangerous.

The agency had said that a decision would be announced by Friday on registering methyl iodide, also known as idomethane. But in an unusual move, it said Friday that officials "will address recent questions prompted by the pending registration of iodomethane."

The agency received a letter this week from 54 scientists, including six Nobel Prize winners, who said they were astonished the EPA was considering approving such a toxic chemical for agricultural use.

"The gratifying thing is that EPA has been responsive to people who are really concerned about this," said Robert Bergman, University of California at Berkeley professor who organized the scientists' letter. The letter criticized the agency's scientific analysis, calling for an independent scientific review of the science.

The fumigant was developed to replace the highly effective fumigant methyl bromide, which is banned by an international treaty because it depletes the earth's ozone layer. Both fumigants are injected into soil before planting and do not leave a residue on the produce itself. Community groups said fumes may escape from the soil and harm farmworkers or nearby residents.

LENA'S COMMENT: Let's hope the FDA doesn't follow it's normal pattern - listens to business interests rather than consumer interests - and is smart and not release this into the world for horrific results for the next generation!


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