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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.
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Email Lena
928-636-9425
Wednesday October 3, 2007
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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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Cool autumn weather is such
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==================================
Something To Think About
============================
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
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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
~^~^~^~^~^~^~^~^~^~^~^
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.
~^~^~^~^~^~^~^~^~^~^
HEALTH TODAY
~^~^~^~^~^~^~^~^~^~^~
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
~^~^~^~^~^~^~^~^~^~^~^~~^~^~^
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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