
Lena
Sanchez Editor
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The American Lung Association says tobacco contains more than 4,000
chemicals, 60 of which causes cancer.
Some of the 'killers' are radioactivity, arsenic, ammonia, lead,
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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 December 17, 2004
````````````````````````````````````````````````````
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============================
=> IN THIS ISSUE!
============================
==> Editors' Ranting & or Warnings
==> Something To Think About
==> Health Thought for the day!
==> Today's Health Spotlight
==> Monthly Spotlight Ads
==> Today's Health Tip
==> Food of The
Week
==> Health Today
==> Environmental Report
==> Life Changing Information
+++++++++++++++++++++
EDITORS' RANTING
+++++++++++++++++++++
Greetings and thank your for subscribing!
Ahhhh! Weekend almost upon me and a day of rest before the final run up
to the holiday and all the work that it entails. Clean beds for family,
specific food for the picky ones, shopping for those special traditional
dishes that can only happen at home, but all done with love and
joy at being healthy and able to do the things to make each guest happy!
My wish for you is, that you can say the same thing... Health is
imperative to enjoying life...
If you missed Wednesday's Christmas Gift to you or would like to have it
in print go to
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Take charge of you and your family's health before it takes charge of
you!
Lena
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==================================
Something To Think About
============================
Just take a look at the great happening when the
majority of people don't get a flu shot!!! But do you think anyone in
the traditional medical world will be able to figure out why the flu is
really rare this year?
Flu-46
By RDF Columnist, Dr. F. Edward Yazbak
http://www.redflagsweekly.com/yazbak.html
Falmouth, Massachusetts, USA
tlautstudy@aol.com
The Centers for Disease Control and Prevention (CDC) publishes weekly
reports during the influenza season. The latest available report (1),
written on November 24, describes the Influenza activity during week 46
of 2004 (November 14 to 20).
The population of the United States was estimated at slightly above
294.8 million that week.
A total of 1,118 specimens were submitted for viral testing to the U.S.
World Health Organization (WHO) and National Respiratory and Enteric
Virus Surveillance System (NREVSS) collaborating laboratories during
that week. Of these, 36 (3.2%) were positive: 9 were influenza A (H3N2)
viruses, 18 were influenza A viruses (not sub-typed), and 9 were
influenza B viruses.
The two laboratories tested 11,899 specimens in all since October. Of
these, 170 (1.4%) were positive: 134 (78.8%) were influenza A and 36
(21.2%) were influenza B viruses. Over 50% of the isolated influenza A
viruses were sub-typed and identified as influenza A-H3N2.
Twenty-three states have not yet had laboratory-confirmed influenza.
Since October 1, the CDC conducted antigenic testing on a total of 11
influenza viral isolates: nine influenza A (H3N2) viruses and 2
influenza B viruses. All of the influenza A (H3N2) isolates were A/Fujian/411/2002-like
(H3N2), the influenza A (H3N2) component in the 2004-05 flu vaccine.
Both influenza B viruses were B/Shanghai/361/2002-like, also the
influenza B component of this year’s vaccine. It is indeed most
fortunate that after this year’s National crisis, we at least seem to
have, based on eleven tests, the right choice of vaccine strain.
According to the CDC, there were fewer visits for “influenza –like
illnesses” in week 46 than the National baseline and so far, there have
been no pediatric “flu-related deaths”.
The flu season started early in the fall of 2003 and the number of cases
peaked between mid-December and mid-January. During week 46 last year,
there were over 1200 isolates nationwide (compared to 36 this year). The
percentage of respiratory specimens testing positive for influenza
peaked at 35.2% during the week ending November 29, 2003. The largest
number of isolates was reported during the week ending December 13. The
peak percentage of specimens testing positive for influenza during the
previous 4 seasons (1999-00, 2000-01, 2001-02, and 2002-03) ranged from
23% to 31%. (2). It is noteworthy that as previously mentioned, only
1.4% of submitted cultures were positive so far this year. It is
obviously possible that the other 88.6% of cultured people did indeed
have the flu, even if their cultures were negative. It is also
conceivable that they did not.
The panic, frenzy and long lines of the earlier weeks have subsided as
more vaccine is becoming available. British manufacturer,
GlaxoSmithKline who produces 10% of the world’s flu vaccine,has applied
for FDA approval for its Fluarix vaccine. Prompt approval is expectedand
GSK could deliver 4 million doses this season and probably more in the
future.
The recommended 2004-05 trivalent influenza vaccine for the United
States contains A/New Caledonia/20/99-like (H1N1), A/Fujian/411/2002-like
(H3N2), and B/Shanghai/361/2002-like viruses. For the A/Fujian/411/2002
(H3N2)-like antigen, manufacturers will use the equivalent
A/Wyoming/3/2003 (H3N2) virus, and for the B/Shanghai/361/2002-like
antigen, manufacturers will use the equivalent B/Jilin/20/2003 virus or
B/Jiangsu/10/2003 virus.
The CDC has several suggestions (3) for those who could not or would not
be vaccinated.
A recently published recipe for chicken soup (4) by the Director of
Pulmonary Medicine at a distinguished Medical Center is also worth
trying.
A review of the whole U.S. Influenza season will be reported to Red
Flags members as soon as it is available.
References
http://www.cdc.gov/flu/weekly/fluactivity.htm (Current weekly
flu report)
http://www.cdc.gov/flu/weekly/weeklyarchives2003-2004/03-04summary.htm
http://www.cdc.gov/flu/professionals/flugallery/images04_05/notonlyway2.pdf
http://news4colorado.com/health/local_story_313165643.html
=======================
THOUGHT FOR THE DAY!
=======================
"To laugh often and much; to win the respect of
intelligent people and the affection of children; to earn the
appreciation of honest critics and to endure the betrayal of false
friends; to appreciate beauty; to find the best in others; to leave the
world a bit better whether by a healthy child, a garden patch or a
redeemed social condition; to know even one life has breathed easier
because you have lived. This is to have succeeded."
~ Ralph Waldo Emerson
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^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^
===========================
TODAY'S HEALTH
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TODAY'S HEALTH TIP
~^~^~^~^~^~^~^~^~^~^~^~
Companies Cutting Health Benefits
Dec 15, 2004
By MARK SHERMAN
WASHINGTON (AP) - Many companies are dropping their promise of health
benefits for future retirees, who now might have to stay on the job
longer and rely on government health care in their old age.
Eight percent of employers with at least 1,000 workers said they had
eliminated subsidized retiree health benefits for some workers this
year, and 11 percent more said they probably would do so next year,
according to a study released Tuesday by the benefits consulting firm
Hewitt Associates and the nonprofit Kaiser Family Foundation.
Most of those affected were newly hired, but some companies said the
change applied to workers who had been on the payroll longer.
The number of companies that offer health coverage to retirees has been
on the decline for 15 years.
But among those that continue to subsidize retiree coverage, the move to
treat current and former workers differently reflects a desire to leave
health benefits in place for those who have already retired despite
several consecutive years of double-digit increases in health care
costs.
Since 2000, more than 100 large employers have chosen this path.
Some have cut out subsidies but have told employees they can continue
coverage under company health plans after they retire, a much cheaper
option than seeking health insurance elsewhere.
"Retiree health care coverage is kind of a slowly vanishing species,"
Kaiser president Drew Altman said.
The prospect of losing health coverage in retirement is troubling
particularly to people who are considering changing jobs or who want to
retire between the ages of 55 and 64. Younger retirees can find it
difficult to afford health insurance when they can't get it from their
employers.
Medicare, the government health program for older and disabled
Americans, kicks in at age 65. Its benefits typically have been less
generous than those offered by employers, mainly because the workplace
plans cover prescription drugs. Medicare's drug insurance program begins
in 2006.
The employer plans, however, are asking retirees to pay more of their
health costs through higher insurance premiums and larger co-pays for
doctor visits and prescription medicines.
People who retire in 2004 face premiums about 25 percent higher than
those who retired last year, according to the survey of 333 companies,
which was conducted between May and September.
Most large employers said they will maintain prescription drug benefits
for retirees after the Medicare drug program begins in 2006, the study
said.
The fate of retirees with employer-sponsored drug benefits was a major
consideration of the authors of last year's Medicare prescription drug
law.
To keep more employers from dropping coverage, the law includes up to
$88 billion over 10 years in tax-free subsidies to companies that offer
prescription benefits that are at least the equal of Medicare's.
In 1991, 80 percent of firms employing 1,000 or more workers offered
health coverage to retirees. By 2003, the number had fallen to 57
percent, Hewitt said. When looking at companies with at least 200
employees, the number is 38 percent, Kaiser said.
Roughly 15 million retirees receive health care coverage from former
employers. About 3 million are 55 to 64. The rest are eligible for
Medicare, Altman said.
The new survey, conducted before issuance of final Medicare regulations
about the drug benefit, found that just 8 percent of employers said they
would drop retirees' drug benefits in the program's first year.
Frank McArdle, manager of Hewitt's research office in Washington, said
the early response from employers is good news. But he cautioned that
decisions about 2007 and beyond would depend on the regulations, the
design of Medicare drug plans devised by private insurers and by costs.
Kaiser Family Foundation
Hewitt Associates
LENA'S COMMENT: This is the very reason you cannot wait until you
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~^~^~^~^~^~^~^~^~^~
FOOD OF THE
WEEK
~^~^~^~^~^~^~^~^~^~
Strange shape, strange names but great taste!
As I rolled the huge pear/ball/grapefruit shaped thing in my hand
debating whether I should try it or not? I decided it would be worth the
risk as it had a thick skin making it less likely to be full of
pesticide chemicals. The name was strange and one I didn't recognize. On
investigation I found out that it carries several names; pomelo =
pummelo = Chinese grapefruit = shaddock! Pronunciation: PUHM-uh-low
- The French name for this fruit is chadec. The current Malayan
names are limau abong, limau betawi, limau bali, limau besar, limau
bol, limau jambua, Bali lemon, and pomelo.
I'll call it a Pummelo as that is what the name on the box said...
Pummelo is the largest of the citrus fruits with a shape that can be
fairly round or slightly pointed at one end -the fruit ranges from
nearly round to oblate or pear-shaped. They range from cantaloupe-size
to as large as a 25-pound watermelon and have very thick, soft rind.
The one I bought was sort of pear shaped and about 10 inches across...
It is known in the western world mainly as the principal ancestor of the
grapefruit The pummelo is popular in the Asia and is new to California
but rarely seen in the Eastern United States.
It's sweeter than a grapefruit. The skin is greenish yellow and slightly
bumpy with the feel of citrus skin; flesh color ranges from pink to
rose.
The pulp is milder and sweeter than its closest cousin, the grapefruit.
Pummelos are available mid-January through mid-February from California.
Can be used in the same manner as any other citrus fruit.
Said to be native to southeastern Asia and all of Malaysia; It is said
to grow wild on river banks in the Fiji and Friendly Islands. It is said
to have been introduced into China around 100 B.C. It is much cultivated
in southern China - Kwang-tung, Kwangsi and Fukien Provinces - and
especially in southern Thailand on the banks to the Tha Chine River;
also in Taiwan and southernmost Japan, southern India, Malaya,
Indonesia, New Guinea and Tahiti.
The pomelo is also called shaddock after an English sea captain, Captain
Shaddock, who introduced the seed to the West Indies in the 17th Century
from the Malay Archipelago. The seeds produced fruit somewhat smaller
than the current grapefruit, more like an orange. The size of the fruit
and the fact that it grew in bunches or clusters like grapes prompted a
19th century naturalist to liken the new fruit to grapes, with which it
has no botanical relationship whatsoever.
Some say the grapefruit is a cross between an orange and the pummelo (or
shaddock), while others believe that grapefruit is a natural mutant
(sometimes referred to as a small shaddock) derived from the seeds
Captain Shaddock brought to the West Indies.
Pummelo skin is also used medicinally in some cultures. For instance, in
Southeast Asia raw pummelo skin pieces are given to patients to eat who
are having problems with excessive coughing and who have a history of
epileptic seizures.
As for the nutrients in a Pummel? Guess it's a mystery as I couldn't
find anything written on the nutrients in one. I am assuming since it's
citrus it has lot of phytonutrients but exactly which ones is a guess...
Since it is used as a medicine in Asia I suspect they are all good!
I ate mine raw and was very good and tasty, just slightly sweeter than a
grapefruit with a very similar taste. I shall be eating more, even if I
don't know exactly what nutrients are in one.
The Experiment in food was well worth it!
Lena
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HEALTH TODAY
^~^~^~^~^~^~^~^~^~^
AIDS Research Chief Altered Safety Report
Dec 15, 2004
By JOHN SOLOMON
WASHINGTON (AP) - The government's chief AIDS researcher removed
some negative safety conclusions from a subordinate's report on
a U.S.-funded drug experiment, then ordered the research to
resume over objections from his staff, memos show.
As justification, Dr. Edmund Tramont, chief of the National
Institutes of Health's AIDS Division, cited his four decades of
medical experience and argued that Africans with an AIDS crisis
deserved some leniency in meeting U.S. safety standards,
according to interviews and documents obtained by The Associated
Press.
Tramont's staff, including his top deputy, had urged more
scrutiny of the Uganda research site to ensure it overcame
record-keeping problems, violations of federal patient safety
safeguards and other issues. These problems had forced a
15-month halt to the research into using a single dose of
nevirapine to prevent African babies from getting AIDS from
their mothers.
AP reported Monday that NIH knew about the problems in early
2002 but did not tell the White House before President Bush
launched a plan that summer to spread nevirapine throughout
Africa.
Now, officials have new concerns the lone dose of nevirapine
may cause long-term resistance to AIDS drugs in the hundreds of
thousands of African patients who received it, foreclosing
future treatment options.
In July 2003, Dr. Jonathan Fishbein, an expert NIH hired to
improve agency research practices wrote Tramont: "I am not
convinced that the (Ugandan) site is indeed prepared to become
active."
Fishbein contended he should be given time to review Uganda's
capabilities and safety monitoring before letting the site
reopen, or NIH would risk being "toothless" in its new efforts
to clean up sloppy research practices. He added that
professional safety monitors hired by NIH had reservations about
the site.
Tramont dismissed the safety monitors' concerns, saying he
didn't believe they fully understood AIDS.
"I am convinced that this site is ready to resume given the
limitations of doing research in any resource-poor,
underdeveloped country," Tramont wrote July 8, 2003, in response
to Fishbein.
"I want this restriction lifted ASAP because this site is now
the best in Africa run by black Africans and everyone has worked
so hard to get it right as evidenced by the fact that their lab
is now certified," he wrote.
NIH officials acknowledge Tramont rewrote the report and
overruled his staff on the reopening, but said he did so because
he was more experienced and had an "honest difference of
opinion" with his safety experts. They noted Tramont had no
financial interest in nevirapine and that the troubled study
began well before he joined NIH in 2001.
Those who raised objections "were part of a large team of which
Dr. Tramont was the head, and it is important that the people
involved in that team should express their opinion and there
should be discussion," said Dr. H. Clifford Lane, the NIH's No.
2 infectious disease specialist and one of Tramont's bosses.
Lane was designated by NIH to speak to AP on Tramont's behalf.
"But at the end of the day, the final responsibility lies with
the head of the team, and it is his job to put that together the
way he sees it," Lane said.
Lane said an internal NIH review concluded Tramont had not
engaged in scientific misconduct. Separately, the National
Academy of Sciences continues to investigate whether the Uganda
research was valid.
NIH believes it helped save hundreds of thousands of African
babies by allowing nevirapine to be used in single doses to
block the AIDS virus, Lane said. But he acknowledged the
research was imperfect, and NIH now believes nevirapine should
no longer be a first choice for newborn protection - if other
options exist - because of the newly discovered problems with
resistance.
One of the nation's premier AIDS charities said Tuesday it is
concerned the controversy over the 2002 study problems will
cause African countries to stop using the drug, and called on
medical experts to find ways to get better new solutions into
the Third World.
"Rather than focus on withdrawing nevirapine from those who
urgently need it, the entire world should focus on how we can
provide the funding for infrastructure improvements, training,
and drug purchase costs so that more and more women will have
access to the most effective drug regimens possible," the
Elizabeth Glaser Pediatric AIDS Foundations said in response to
AP's stories.
Tramont wrote in 2003 e-mails that he reopened the clinics
because he didn't want NIH "perceived as bureaucratic but rather
thoughtful and reasonable" and that it was important to
encourage Africans' fight against AIDS "especially when the
president is about to visit them."
Bush visited the continent a few days after Tramont ordered the
clinics reopened.
Tramont's actions, however, drew criticism from his top deputy.
"I think we are cutting off our noses to spite our face here,"
AIDS Division Deputy Director Jonathan Kagan wrote. "... We
should not be motivated by political gains and it's dangerous
for you, of all people, to be diminishing the value of our
monitors." Tramont prevailed.
Five months earlier, Tramont surprised one of his own medical
officers, who had written a report summarizing safety concerns
uncovered during a second review of the Uganda trial.
Dr. Betsy Smith's report, finished in January 2003, said the
Uganda trial suffered from "incomplete or inadequate safety
reporting" and records on patients were "of poor quality and
below expected standards of clinical research."
She strongly urged NIH not to make sweeping conclusions about
nevirapine based on the Uganda research. "Safety conclusions
from this trial should be very conservative," she wrote.
Behind the scenes, Tramont asked to see Smith's report before it
was submitted to medical authorities, including the Food and
Drug Administration. "I need to see the primary data - too much
riding on this report," Tramont wrote Jan. 23, 2003.
A few weeks later, the safety report was published and sent to
FDA without Smith's concerns and with a new conclusion.
The study "has demonstrated the safety of single dose nevirapine
for the prevention of maternal to child transmission," Tramont's
version concluded. "Although discrepancies were found in the
database and some unreported AEs (adverse reactions) were
discovered ... these were not clinically important in
determining the safety profile."
In disbelief, Tramont's staff began inquiring how Smith's report
got changed. An answer came back from the top.
"I wrote it," Tramont responded.
Documents gathered by AP for this story are available at:
http://wid.ap.org/documents/nevirapine2.html
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^~^~^~^~^~^~^~^~^~^~^~^~^~^~^
ENVIRONMENTAL REPORT
~^~^~^~^~^~^~^~^~^~^~^~~^~^~^
I'm making my comment before you read this article
to prepare you: The story made me laugh so hard I almost wet my pants...
Having lived in the country for the last 13 years and most of my
childhood and living with mice while trying to keep them from over
populating, The site of these so-called scientists running around trying
to catch the millions of mice that populate the countryside and cities
was too funny for words. A great visual for the mind and my healthy dose
of laughter for the day, as well as a reminder of the asinine mind set
of some medical scientists in their moments of insanity... There are so
many vaccines for every type of disease and illness anymore that I
shutter to think of the consequences of human beings being filled with
so many vaccines and the side effects that will be occurring!
Vaccinating Mice Could Reduce Lyme Disease
December 15, 2004
WASHINGTON - Vaccinating mice against Lyme disease may help protect
people against the infection, which is often spread from mice to humans,
U.S. researchers said on Monday.
The study is one of the first to show that immunizing a wild animal that
carries a disease might serve to protect humans, the National Institute
of Allergy and Infectious Diseases said.
"When integrated with other protective measures, this strategy could
have significant implications, not only for preventing Lyme disease, but
for preventing other vector-borne diseases as well, including plague and
West Nile virus," said NIAID head Dr. Anthony Fauci.
Lyme disease is caused when people are bitten by a tick carrying the
Borrelia burgdorferi bacteria.
It affected 23,000 Americans in 2002 and causes a characteristic
"bull's-eye" rash, fatigue, chills and fever, headache, muscle aches and
joint pain. Untreated, it can lead to more severe symptoms and
arthritis.
It passes from mice and other small rodents to people via black-footed
ticks. Often deer are involved.
It would be necessary to develop a vaccine that could be given orally,
probably in mouse bait, the researchers report in this week's issue of
the Proceedings of the National Academy of Sciences.
For their study, the team at Yale University and elsewhere caught 1,000
white-footed mice, drew their blood, examined the ticks in their fur and
then vaccinated half of them.
When an infected tick nymph feeds on an immunized mouse, the mouse's
immune system kills the bacteria inside the nymph.
After vaccinating the mice, the researchers found 55 percent fewer tick
nymphs were infected.
But they also found that mice are not the only carriers.
"We've learned we shouldn't naively ignore other hosts -- shrews,
chipmunks, robins, and maybe others," said Jean Tsao, now at Michigan
State University, who worked on the study.
"The targeted vaccination of wildlife carriers could offer more
far-reaching protection against vector-borne diseases than vaccinating
humans," added Dr. Alan Barbour at the University of California, Irvine,
who helped lead the study.
"When the vaccine is targeted to humans, only those who experienced a
satisfactory immune response to the vaccine are protected; however, when
the vaccine is targeted to wildlife carriers, the risk of infection is
lowered for everyone in the community."
REUTERS NEWS SERVICE
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