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"A NATURAL ENVIRONMENTAL HEALTH FACTS Ezine"
Here to Inform and Help You Become Healthier and Happier while Achieving Quality
Longevity!
http://www.antibiotic-alternatives.com
Email Lena
928-636-9425
Friday June 30, 2006
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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!
We are headed out of here to
the really hot country of Phoenix for the weekend. Ordinarily we stay
away from there in the summer but a brother-in-law is celebrating 50
years of marriage to his love and we will be there to enjoy that
celebration so Sunday's ANEH Facts will be out late Sunday evening when
we return. Have a great week and don't forget your day of rest... Change
of pace in your life can mean the difference in rest or not!
If you have a question or comment (good or
not so good) send it to me...
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Take charge of you and your family's health before it takes charge of
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Lena
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Something To Think About
============================
MERCK'S GARDASIL VACCINE NOT
PROVEN SAFE FOR LITTLE GIRLS
National Vaccine Information Center Criticizes FDA for Fast Tracking
Licensure
Washington, D.C. - The National Vaccine Information Center (NVIC) is
calling on the CDC's Advisory Committee on Immunization Practices (ACIP)
to just say "no" on June 29 to recommending "universal use" of Merck's
Gardasil vaccine in all pre-adolescent girls. NVIC maintains that
Merck's clinical trials did not prove the human papillomavirus (HPV)
vaccine designed to prevent cervical cancer and genital warts is safe to
give to young girls.
"Merck and the FDA have not been completely honest with the people about
the pre-licensure clinical trials," said NVIC president Barbara Loe
Fisher.
"Merck's pre and post-licensure marketing strategy has positioned mass
use of this vaccine by pre-teens as a morality play in order to avoid
talking about the flawed science they used to get it licensed. This is
not just about teenagers having sex, it is also about whether Gardasil
has been proven safe and effective for little girls."
The FDA allowed Merck to use a potentially reactive aluminum containing
placebo as a control for most trial participants, rather than a
non-reactive saline solution placebo. A reactive placebo can
artificially increase the appearance of safety of an experimental drug
or vaccine in a clinical trial.
Gardasil contains 225 mcg of aluminum and, although aluminum adjuvants
have been used in vaccines for decades, they were never tested for
safety in clinical trials. Merck and the FDA did not disclose how much
aluminum was in the placebo.
Animal and human studies have shown that aluminum adjuvants can cause
brain cell death and that vaccine aluminum adjuvants can allow aluminum
to enter the brain, as well as cause inflammation at the injection site
leading to chronic joint and muscle pain and fatigue. Nearly 90 percent
of all Gardasil recipients and 85 percent of aluminum placebo recipients
reported one or more adverse events within 15 days of vaccination,
particularly at the injection site. Pain and swelling at injection site
and fever occurred in approximately 83 percent of Gardasil and 73
percent of aluminum placebo recipients. About 60 percent of those who
got Gardasil or the aluminum placebo had systemic adverse events
including headache, fever, nausea, dizziness, vomiting, diarrhea,
myalgia. Gardasil recipients had more serious adverse events such as
headache, gastroenteritis, appendicitis, pelvic inflammatory disease,
asthma, bronchospasm and arthritis.
"Merck and the FDA do not reveal in public documents exactly how many 9
to 15 year old girls were in the clinical trials, how many of them
received hepatitis B vaccine and Gardasil simultaneously, and how many
of them had serious adverse events after being injected with Gardasil or
the aluminum placebo. For example, if there were fewer than 1,000 little
girls actually injected with three doses of Gardasil, it is important to
know how many had serious adverse events and how long they were followed
for chronic health problems, such as juvenile arthritis."
According to the Merck product manufacturer insert, there was 1 case of
juvenile arthritis, 2 cases of rheumatoid arthritis, 5 cases of
arthritis, and 1 case of reactive arthritis in 11,813 Gardasil
recipients plus 1 case of lupus and 2 cases of arthritis out of 9,701
participants primarily receiving an aluminum containing placebo.
Clinical trial investigators dismissed most of the 102 Gardasil and
placebo associated serious adverse events, including 17 deaths, that
occurred in the clinical trials as unrelated.
"There is too little long term safety and efficacy data, especially in
young girls, and too little labeling information on contraindications
for the CDC to recommend Gardasil for universal use, which is a signal
for states to mandate it," said Fisher. "Nobody at Merck, the CDC or FDA
knows if the injection of Gardasil into all pre-teen girls - especially
simultaneously with hepatitis B vaccine - will make some of them more
likely to develop arthritis or other inflammatory autoimmune and brain
disorders as teenagers and adults. With cervical cancer causing about
one percent of all cancer deaths in American women due to routine pap
screening, it was inappropriate for the FDA to fast track Gardasil. It
is way too early to direct all young girls to get three doses of a
vaccine that has not been proven safe or effective in their age group."
The National Vaccine Information Center (NVIC), founded in 1982 by
parents of vaccine injured children, has been a leading critic of
one-size-fits-all mass vaccination policies and the lack of basic
science research into biological mechanisms and high risk factors for
vaccine-induced brain and immune system dysfunction. As a member of the
FDA Vaccines and Related Biological Products Advisory Committee (VRBPAC),
Barbara Loe Fisher urged trials include adequate safety data on
pre-adolescent children and warned against fast tracking Gardasil at the
November 28-29, 2001 VRBPAC meeting.
http://www.fda.gov/ohrms/dockets/ac/cber01.htm# Section: Vaccines
& Related Biological
=======================
THOUGHT FOR THE DAY!
=======================
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TODAY'S HEALTH TIP
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Did You Buy Into The
Latest Attempt to Discredit Natural Medicine?
Headline read;
"Fish Oils may Not Protect Hearts"
"Fish Oil Won't Fix Abnormal Heart Rhythms: Study"
Those headline came about because researchers at the Wageningen
Centre for Food Science in the Netherlands recruited 546 subjects
with arrhythmias to take two grams of fish oil per day or a placebo.
On average, the intervention group took the fish oil supplement for
356 days. The conclusion: "Our findings do not indicate evidence of
a strong protective effect of intake of omega-3 PUFAs from fish oil
against ventricular arrhythmia in patients with ICDs."
ICDs - that's one little wrinkle I didn't mention. ALL subjects had
implantable cardioverter-defibrillators (ICDs) and they all had been
diagnosed with either malignant ventricular tachydardia (VT) or
ventricular fibrillation (VF).
The patients were so sick that they already had ICDs implanted
within them! The evaluation was testing fish oil against malignant
VT, the second worst type of arrhythmia; VF, the absolute worst,
deadliest, hardest to get and hardest to stop arrhythmia; and sudden
death! Even drugs won't work against VF once a person gets it, which
is the only reason why you'd EVER surgically implant an ICD in a
person in the first place!
LENA'S COMMENT: You need to know there are different types of
arrhythmia. Some not so immediately life threatening and some
immediately life threatening. It would seem the people chosen had
already gone into the realm of life threatening and beyond
prevention mode... Another flaw; Only 2 grams of fish oil was used.
That isn't enough to help anyone healthy or ill! 6 grams, minimum,
would have given them a better chance of succeeding could anything
have helped those people in the test. I came to the conclusion that
study was done just for discrediting natural medicine! FYI; The
majority if not all arrhythmia's can be averted by keeping
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HEALTH TODAY
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Telling The Truth Can Be Dangerous
To A Doctor's Profession!
Even in the
so-called enlightened world outside the U.S.A. the drug industry
has it's fangs out and is waiting to pounce. Dr. Andrew
Wakefield, the physician who published a paper in 1998 showing a
link between the measles, mumps and rubella (MMR) vaccine and
autism, is being charged with professional misconduct by the
UK's General Medical Council.
The Council's preliminary charges include:
- Publishing
"inadequately founded" research
- Failing to obtain
ethical committee approval
- Obtaining funding
"improperly"
- Subjecting children to
"unnecessary and invasive investigations"
While small U.S. studies have found a similar link between MMR
and autism, major studies have not proven the link. Nonetheless,
after Wakefield's paper was published, MMR immunization rates
fell (but have since picked up).
The paper was originally published in The Lancet, but was later
removed. Wakefield was reportedly being paid to find out whether
evidence existed to support potential legal action by parents
who claimed their children had been hurt by the MMR vaccine.
BBC News June 12, 2006
The Independent June 12, 2006
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ENVIRONMENTAL REPORT
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Justices Agree to
Consider New Case on Emissions
By
MICHAEL JANOFSKY
June 27, 2006
WASHINGTON, June 26 - The Supreme Court
agreed Monday to decide whether the federal government is required to
control vehicle emissions of carbon dioxide, the principal greenhouse
gas that scientists have linked to
global warming.
In accepting a petition from states, cities and environmental groups,
the justices agreed to hear arguments on whether the Clean Air Act
requires the
Environmental Protection Agency to regulate carbon dioxide and other
gases as air pollutants that may affect public health or the climate.
The case is one of the biggest environmental tests yet for the Bush
administration, which has steadfastly opposed binding controls on
greenhouse gases, instead calling for a voluntary approach by industry
to curb emissions.
"At stake in this case is nothing less than the survival of the earth as
we know it," said
Richard Blumenthal, the attorney general of Connecticut, which sued
the government in 1999 along with New York, New Jersey, nine other
states, three cities and a dozen environmental advocacy groups,
including the
Sierra Club, the
Natural Resources Defense Council and Environmental Defense.
Ten other states and several industry groups joined the side of the
administration.
The case began in the final year of the Clinton administration, when a
group of states and environmental organizations petitioned the E.P.A. to
regulate carbon dioxide. After four years of study, the agency refused,
concluding that the Clean Air Act did not require it to regulate
emissions to prevent climate change.
The law, which was first written in 1963 and revised in 1970, before
global warming emerged as a widespread concern, names many specific
pollutants that the agency must regulate, including compounds released
by cars, factories and power plants that form soot and smog. It does not
name carbon dioxide, and in updating the law in 1990, Congress did not
add the gas.
The plaintiffs have argued that the law's definitions and other terms
implicitly allow the regulation of carbon dioxide as a pollutant.
The administration's refusal to do so reflected a reversal of sorts for
President Bush, who campaigned in 2000 on the need for federal emissions
standards on a variety of air pollutants, including carbon dioxide.
On Monday at the White House, Mr. Bush acknowledged that global warming
was "a serious problem," but he also said there was some debate over
whether it was caused by human activities. He called for using new
technologies for environmental reasons and to wean the nation from its
reliance on oil.
After the E.P.A. announced its refusal to regulate carbon dioxide
emissions in 2003, the plaintiffs filed for review in the United States
Court of Appeals for the District of Columbia Circuit. Last July, three
judges issued three different opinions, which had the effect of
supporting the agency's refusal by a 2-to-1 vote.
Judge David B. Sentelle said the plaintiffs did not have standing to
seek judicial review. Judge A. Raymond Randolph said that even if the
agency had the authority to regulate carbon dioxide, it could choose not
to do so for other reasons, like the uncertainty of the science or
questions over available technologies.
Only Judge David S. Tatel said the law was clear that the agency was
required to regulate emissions when public health and climate
considerations were at issue.
Beyond its effect on federal policy, the case holds important
implications for California and 10 other states that have assumed that
the Clean Air Act authorizes regulations for carbon dioxide and other
gases and have adopted their own stringent limits for automobile and
truck emissions. The state laws, scheduled to go into effect for the
2009 model year, have been challenged in court by automakers.
A ruling by the Supreme Court could influence another case currently
before the same appeals court, involving many of the same plaintiffs.
They are arguing that the E.P.A. should also regulate carbon emissions
from power plants.
A spokeswoman for the E.P.A., Jennifer Wood, said the agency had made
the right decision in refusing to regulate carbon dioxide and defended
its advocacy of a voluntary approach to curbing emissions.
"The president's policy achieves near-term reductions while investing in
long-term solutions," Ms. Wood said in a statement. "In 2004, E.P.A.'s
voluntary partnerships prevented over 60 million metric tons of
greenhouse gas emissions, equivalent to the annual emissions from over
40 million vehicles."
David Bookbinder, a senior lawyer for the Sierra Club, said the Supreme
Court's willingness to hear the case reflected the urgency of the issue.
"It clearly indicates that they are acknowledging the importance of
climate change as a public policy matter," Mr. Bookbinder said.
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