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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Email Lena

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Wednesday  April 11, 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!

Mother Nature as really gone beserk on this continent! We are back to warmer than normal temperatures while the midwest, north and east is freezing with abnormal cold temperatures. All this makes for risky health and hopefully you will take precautions to assure that happens for you...If you take care of your body it will give you many healthy and happy years of service!!! Two supplements that everyone over the age of 10 years needs to be doing for the maximum benefit - daily Balanced minerals and MegaNutrient Vitamins and balance the natural flora! Simple effective and great health producing benefits!

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

ANEH Facts archives  Click Here 
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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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Hypoglycemia and Visual Loss!

New research shows that the sight-damaging effects start even before full-blown diabetes has set in.

In the study, researchers from SUNY Upstate Medical University examined the visual acuity of mice that had been bred to be hypoglycemic. They found that as the mice aged, they not only lost retinal function, but they actually experienced cell death in their retinas. And the worse the hypoglycemia, the worse the vision problems.

The trick here is to determine whether or not you're hypoglycemic and to recognize the symptoms of plummeting blood sugar levels so that you can keep dramatic retina-damaging swings from happening in the first place. This little bit of knowledge could save your vision and keep you from ever developing diabetes.


LENA'S COMMENT: I've found that nutrition is extremely important for vision health! Bad diet and lack of nutrient balance creates hypoglycemia. Can be corrected if caught soon enough and supplements the body's nutrients can assure eye health as well as the rest of the body's organs...


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THOUGHT FOR THE DAY!
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For the next few ezines I will outline omissions in teaching our medical professionals that are creating illness and disease by those very omissions and what they are!

Omission #1. The body must maintain an adequate mineral supply to maintain a balance between internal and external pressures of the body cells called "osmotic equilibrium." This state must be maintained for normal cell function and continued youthful health. The body does not absorb Pill/rock minerals and only assimilates about 1% to 2% into your system. That fact making it imperative to take balanced liquid/powder/caplet form of balanced minerals that contain 84 minerals and trace minerals for 99.9% absorption DAILY to assure that necessary "osmotic equilibrium"!


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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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SHOWCASE SPOTLIGHT 

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How did the Japanese become the longest-living people on Earth?

*Why are their cancer rates are one sixth those of America’s.

* Heart disease and cholesterol-clogged arteries are nearly unheard of, yet these are America’s number one killers.

* Menopause and osteoporosis rates are also ridiculously less than here in the West.


The Japanese take more of this pure dynamite “SUPER FOOD” per person than Americans take of Vitamin C. They take it religiously, each and every day in a tiny capsule that contains a veritable ‘smorgasbord’ of life itself.

What is it called?
Miracle Marine Phyto-Plankton Whole Food Complex Known to;

  • Drop Cholesterol levels like a stone
  • Aching joints become less stiff
  • Blood pressure levels normalized
  • Loss of energy disappears, patients discover their old “get up and go”
  • Skin problems go away as the skin re-discovers the Fountain of Youth found in the ocean
  • Immune system builder
  • Healer of gastrointestinal ulcers
  • Regulates the digestive system
  • Stimulates growth and increases healing in damaged tissue
  • Slows down the aging process
  • Protects against radiation
  • Rids the body of Cadmium, Lead, Mercury, PCB and pesticides.

And none of this comes from a health killing chemical drug. It comes from the ocean, the birthplace of all life

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MONTHLY SPOTLIGHTs 
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* Healthy Skin Means Ignoring Some Well Known skin Care and Cosmetics Products!
*
A UK advocacy group claims that the average woman who wears mainstream cosmetics may be absorbing as many as 175 toxic chemicals every day! Some of these (like formaldehyde, the stuff they use to preserve dead tissues) have been linked to serious health problems - including cancer.

Get Lena's Favorite Healthy Natural Skin Care And Cosmetics & LOOK YEARS YOUNGER IN 30 DAYS!
Click Here

 

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 TODAY'S HEALTH TIP

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How should you treat your child's fever? Maybe you shouldn't ask.

As reported in Pediatrics, researchers at Winthrop University Hospital in Mineola, N.Y., surveyed 161 physicians about how they treat fevers. Most doctors said they start treatment when a young patient's temperature reaches 101 degrees.

And half said they alternated between doses of acetaminophen (Tylenol) and ibuprofen (Advil or Nuprin).

When the doctors were asked why they switched between those two drugs, almost a third said they were following a recommendation by the American Academy of Pediatrics.

But according to the researchers, the American Academy of Pediatrics never issued any such advisory. In fact, the study's authors say, there have been no definitive studies on the best way to treat a fever -- in either children or adults.

LENA'S COMMENT: For what I learned while watching the medical profession treating fevers; read The Necessary Fever
to understand a child's fever, learned from experience and years working in pediatrics.
 


COMMON CHRONIC HEALTH PROBLEMS SOLVED NATURALLY WITH Dr. Garland's Herbal Healthy Repair Kits


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 HEALTH TODAY
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It's About Time!

IBS Drug Zelnorm Taken Off U.S. Market FDA: Voluntary Withdrawal Due to Risk of Heart Attack, Stroke, Chest Pain
By Todd Zwillich


March 30, 2007 -- A popular drug for irritable bowel syndrome and constipation was pulled from the U.S. market Friday 3/30/2007 amid new evidence that it raises the risk of heart attacks and strokes.

Novartis, the manufacturer of Zelnorm, confirmed that Food and Drug Administration officials asked for the drug?s withdrawal.

Agency officials said they based their decision on a Swiss government analysis of 29 Zelnorm studies that showed a higher chance of cardiovascular events, such as heart attack, stroke, or severe heart-related chest pain in patients treated with Zelnorm compared with those given a placebo.

The analysis turned up 13 cases of heart attack, stroke, or angina (chest pain related to heart disease) in about 11,600 patients who took the drug. One of the 13 died, the agency said. This was compared with just one nonfatal event in more than 7,000 patients who took the placebo.

John Jenkins, MD, head of the FDA's Office of New Drugs, described the overall number of dangerous events as "quite small." But he said the rate of cardiovascular events -- about 10 times higher in patients taking Zelnorm -- raised alerts about the drug.

"Based on our review of the data we believed that the risk vs. benefit profile for Zelnorm was no longer favorable," Jenkins told reporters on a conference call.

He said patients taking Zelnorm should speak immediately to their doctors.

Special Access to Zelnorm

Though the drug will no longer be widely available, patients who have no other treatment options could still get access to the drug. The FDA said it is likely to allow Novartis to continue selling Zelnorm to patients if their doctors say they have disease that does not respond to any other treatment and if the benefits of treatment with Zelnorm outweigh the risks of serious side effects. Drug access would be done through a special program.

The FDA says it has told Novartis that it's willing to consider limited reintroduction of Zelnorm at a later date if a population of patients can be identified in whom the benefits of the drug outweigh the risks.

However, before the FDA makes a decision about limited reintroduction, any proposed plan would be discussed at a public advisory committee meeting.

In a statement, Novartis maintained that no evidence proves that Zelnorm caused heart attack or strokes and that event rates were not significantly different from those in the general population. But the company confirmed it would pull Zelnorm from the market.

"Novartis has suspended the marketing, sales, and distribution of Zelnorm in response to the FDA's request," the statement read.

Novartis is a WebMD sponsor.

Zelnorm was approved for short-term treatment of women with irritable bowel syndrome (IBS) with constipation and for patients younger than 65 years with chronic constipation.


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    ENVIRONMENTAL REPORT      
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LENA'S COMMENT: Our leaders are lacking in changing our health outlook!!!!Don't expect environmental improvement anytime soon as the headlines below indicate! Any facility that takes government money for any reason qualifies in this category making for thousands of facilities not reporting leaving us in the dark!

BUSH ORDER REVOKES CLINTON TRI REQUIREMENTS FOR FEDERAL FACILITIES
By Douglas P. Guarino

A recent executive order signed by President Bush revokes Clinton-era measures requiring federal facilities to report their pollution releases to EPA's Toxic Release Inventory (TRI), which the agency uses for a slew of regulatory decisions governing water quality, emissions and other regulatory requirements.

While the White House Council on Environmental Quality (CEQ) is drafting guidance that a spokeswoman says will continue to require federal facilities to report TRI releases, environmentalists are concerned that it could further diminish TRI data after EPA issued a controversial regulation last December that  scales back industry's reporting requirements.

Environmentalists say that if the upcoming CEQ guidance does not clarify that federal facilities must still report to TRI, they will call on Democratic lawmakers to mandate federal facility TRI reporting in pending legislation seeking to block EPA's new regulation from taking effect.

Rep. Frank Pallone (D-NJ), one of the sponsors of the pending legislation, told reporters March 22 that Democrats may seek to attach the TRI legislation to must-pass appropriations legislation later this year. Last year, the House approved similar legislation as an amendment to the fiscal year 2007 Interior and Environment Appropriations bill.

The legislation could gain a further boost after EPA unveiled TRI data for 2005, which shows a three percent increase overall in total disposal and other releases. "Annual changes are not unusual," EPA said in a March 22 press release, saying that possible reasons for the increase include production increases, fluctuations in the content of raw materials used in particular industries and changes in releases at large facilities that impact the national data. Relevant documents are available on InsideEPA.com.

Executive Order (EO) 13423, which the Bush administration published in the Federal Register Jan. 26, revokes EO 13148, which former President Clinton issued April 21, 2000. Section 501 of the Clinton order required federal facilities to report to TRI under section 313 of the Emergency Planning & Community Right-to-Know Act (EPCRA).
 
Environmentalists are raising concerns federal facilities may be exempt from all TRI reporting in the future as a result of the Bush order, given that federal facilities are not required to report to TRI by law. The exact impact of the order, however, will largely depend on what guidance CEQ issues to EPA and other federal agencies on how to implement the order, activist sources say.

"Given that E.O. 13148 was the only order still in place requiring federal facilities to report under the TRI program, Bush's new order may exempt all federal facilities from reporting to TRI in the future," an analysis of the order prepared by the activist group OMB Watch says.

A CEQ spokeswoman says federal facilities are still required to report to TRI despite the Bush executive order. The CEQ spokeswoman says TRI reporting requirements under previous executive orders will continue despite the order. The spokeswoman expects CEQ will issue guidance within "the next week or so" that "should spell out implementation requirements" for the new order.

Environmentalists say they are concerned about the possibility of a TRI exemption for federal facilities due to the significant amount of toxic releases from Defense Department (DOD) and Energy Department (DOE) facilities. "In 2004, the most recent year of TRI data, 313 federal facilities reported 90 million pounds of toxic chemicals released to the air, water and land," according to OMB Watch.

Activists are particularly concerned about air releases from coal-fired power plants under the Tennessee Valley Authority, one environmentalist adds. The Tennessee Valley Authority had more than 69 million pounds of TRI releases in 2004, the environmentalist says.

Controversy surrounding the executive order comes as Pallone and other Democrats are vowing to pass legislation that would block EPA from implementing its rule scaling back TRI reporting requirements for industry. The rule, which EPA finalized Dec. 18, raises the reporting threshold for chemical releases under TRI from 500 pounds to 2,000 pounds and for the first time allows facilities that manage up to 500 pounds of persistent bioaccumulative toxins (PBTs) to use a simplified reporting format.

Sens. Frank Lautenberg (D-NJ) and Robert Menendez (D-NJ), together with Pallone and Rep. Hilda Solis (D-CA), have introduced bicameral legislation that would block EPA's regulation from taking effect.

During a March 22 conference call, Pallone told reporters that Democrats may seek to attach the legislation to appropriations language later this year.

Pallone told reporters the first step for the bill in this Congress would be for the House Energy & Commerce environment subcommittee to host a hearing on the legislation, but said he had not yet secured a date for a hearing due to a slew of recent budget hearings that have occupied the committee's schedule. Asked if full committee chairman John Dingell (D-MI) supported the legislation, Pallone said Dingell "for the most part has been pretty supportive of community right to know over the years."

Pallone and Solis participated in the conference call in order to announce the release of a new analysis of 2004 TRI data prepared by the activist group U.S. PIRG, Toxic Pollution and Health. The lawmakers said the study, which analyzes chemical releases reported by TRI and categorizes them by known health effects, is an example of the type of information that will be limited if EPA's new rule is allowed to go forward.

The environmentalist says the study, along with recent reports that the rule will lead to significant decreases in agency estimates of national environmental and human health risks, will help bolster arguments in support of the legislation.

An informed source familiar with modeling EPA conducted prior to releasing the rule told Inside EPA recently that scaled-back reporting would result in a decrease of 10 to 20 percent of calculated potential risk nationally using some agency assessment tools, even though EPA estimates the new rule will only result in a 1 percent decrease in reported releases. Alterations to EPA data on potential risks are significant because federal, state and local regulators use the data to set enforcement and air monitoring priorities.

A supporter of the rule argues that a 2004 study prepared for the Small Business Administration (SBA) shows that "for 99 percent of all of the nation's 3,142 counties, the changes in reported risk are not significant." However, the same report shows that reported risks for some counties, such as Arapahoe, CO, will decline by nearly 80 percent under the new thresholds using EPA models. Charleston, SC, will lose nearly 70 percent of its reported risks, according to the study, and Caddo, LA, will lose nearly 60 percent.

 


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