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If you
are done taking risks with your pets health and life by buying mass
marketed, store bought pet food brands
click here to learn about or buy SAFE
Holistic Health food for dogs and cats...which contain NO wheat, NO corn,
NO antibiotics, NO steroids, NO gluten and NO by-products of any kind. You
may also want to
click
on this link to enter the home of HealthyPetNet.
You Should Know...
"HealthyPetNet" receives the ingredients for their foods
and treats just a day or two before they're cooked. The food is cooked at
212 degrees for only 12.5 seconds! This extremely fast hardening process
helps to protect the food's nutritional integrity!
The “HealthyPetNet” facility does NOT use
pesticides indoors. The only pest control used is outside the building,
away from all foods, treats and raw ingredients!
“Life’s Abundance” foods and treats
are considered hypo-allergenic, because they never have and never will
contain allergy causing corn or wheat. You NEVER have to worry about toxic
mold from corn or wheat, either!

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Recalls, Alerts and More...

Quick Jump Links:
FDA Approved "Madness" -
Mercury Contaminations
- What is
"Iatrogenocide"?!
- 911

"3
Companies Indicted Over Tainted Pet Food"
One
U.S. business among those accused of importing a toxic ingredient
Contaminated Pet Foods Have Affected at Least 39,000 Dogs and Cats
Nationwide, Report Says
The number of cases
of kidney failure among dogs and cats that ate poisoned pet food could
total in the tens of thousands says Dr. Paul Pion, president of the Veterinary
Information Network. More accounts of stricken pets had been coming in
since the numbers were tallied over the weekend.
Click here for Nationwide Class Action Lawsuit Filed
Against Pet Food
Companies and Retailers For Misleading Consumers Regarding the Contents of Pet
Food
Click here for current "FDA Pet Food Recall Notices"
(by Company Name)
Menu Foods
Del Monte Pet Products
Hills Pet Nutrition
Nestlé Purina PetCare Company
Sunshine Mills, Inc.
Natural Balance Pet Foods, Inc.
Cereal Byproducts Company
Royal Canin USA
CJ Foods
SmartPak
Chenango Valley Pet Foods
American Nutrition, Inc.
-
American Nutrition, Inc. Issues Voluntary Recall (April 26, 2007)
-
Blue Buffalo Company, Ltd Issues Nationwide Recall of "Blue" Canned Dog
Foods, "Blue Spa Select" Canned Cat Foods and "Blue" Dog Treats Manufactured
at American Nutrition, Inc. (April 27, 2007)
- Sierra
Pet Products, LLC Issues Nationwide Recall of "Harmony Farms" Canned Dog
Foods, "Harmony Farms" Canned Cat Foods and "Harmony Farms" Dog Treats
Manufactured at American Nutrition, Inc. (April 27, 2007)
-
Natural Balance Pet Foods, Inc. Recalls Products in Response to American
Nutrition Inc. Pet Food Recall (April 27, 2007)
- Diamond
Pet Food Withdraws Products in Response to American Nutrition Inc. Pet Food
Recall (April 26, 2007)
Diamond Pet Food

JULY 26, 2007
HEAD'S UP regarding "Dick Van Patten Dog Foods:
Date:Thursday, July 26, 2007, 9:21 AM Subject:Dog food
recall
Everyone with dogs...If you are using the
Dick Van Patten "Natural" dog foods, be SURE to look at this link to the FDA
recall page:
http://www.fda.gov/bbs/topics/NEWS/2007/NEW01670.html

Updated May11, 2007
We now know that this recent pet food recall
was off the charts when it comes to dastardly doings. It appears that the SNAFU
is still unsettled and thousands of animals have died...
March 16, 2007
Pet Food Recalled...Click on
link below for detail:
Warning For Pet Owners: Huge Recall on Dog & Cat Food
visit site
 
wten.com
A warning out there for pet owners: a dog food company is
recalling 60-million containers of wet dog and cat food."Menu Foods,"
producers of "Iams" says it has received reports of cats and dogs suffering
kidney failure after eating the food...

CDC tracks peanut
butter contamination
By MIKE STOBBE, AP
Medical WriterThu Feb 15, 6:47 PM ET
Government
scientists struggled Thursday to pinpoint the source of the first U.S.
salmonella outbreak linked to peanut butter, the kid favorite packed into
millions of lunchboxes every day.
Nearly 300 people in
39 states have fallen ill since August, and federal health investigators
said they strongly suspect Peter Pan peanut butter and certain batches of
Wal-Mart's Great Value house brand — both manufactured by ConAgra Foods Inc.
Shoppers across the
country were warned to throw out jars with a product code on the lid
beginning with "2111," which denotes the plant where it was made.
How the dangerous
germ got into the peanut butter was a mystery. But because peanuts are
usually heated to high, germ-killing temperatures during the manufacturing
process, government and industry officials said the contamination may have
been caused by dirty jars or equipment.
"We think we have
very strong evidence that this was the brand of peanut butter. Now it goes
to the next step of going to the place where the peanut butter was made and
focusing in on the testing," said Dr. Mike Lynch, an epidemiologist at the
Centers for Disease Control and Prevention.
The suspect peanut
butter was produced by ConAgra at its only peanut butter plant, in
Sylvester, Ga., federal investigators said.
ConAgra said it is not clear how many jars are affected by
the recall. But the plant is the sole producer of the nationally distributed
Peter Pan brand, and the recall covers all peanut butter — smooth and chunky
alike — produced by the plant from May 2006 until now.
"We're talking a lot of jars of peanut butter," said Dr.
David Acheson, chief medical officer of the Food and Drug Administration's
Center for Food Safety and Applied Nutrition.
FDA inspectors visited the now shut-down plant Wednesday and
Thursday to try to pinpoint where the contamination could have happened. The
FDA last inspected the plant in 2005. Testing was also being done on at
least some the salmonella victims' peanut butter jars, but investigators
said some may have already been discarded.
The highest number of cases were reported in New York,
Pennsylvania, Virginia, Tennessee and Missouri. About 20 percent of all the
ill were hospitalized, and there were no deaths, the CDC said.
About 85 percent of the infected people said they ate peanut
butter, and about a quarter of them ate it at least once a day, the CDC's
Lynch said. It was the only food that most of the patients had all recently
eaten.
"We think there's very strong evidence that it was this
brand of peanut butter," Lynch said.
Salmonella sickens about 40,000 people a year in the U.S.
and kills about 600. It can cause diarrhea, fever, dehydration, abdominal
pain and vomiting.
But most cases of salmonella poisoning are caused by
undercooked eggs and chicken. The only known salmonella outbreak in peanut
butter — in Australia during the mid-1990s — was blamed on unsanitary plant
conditions.
ConAgra spokesman Chris Kircher said the company randomly
tests 60 to 80 jars of peanut butter that come off its Sylvester plant's
line each day for salmonella and other germs, and "we've had no positive
hits on that going back for years." But he said the plant was shut down as a
precaution for further investigation.
"We're trying to understand what else we need to do or
should be doing," Kircher said.
An estimated 974 million pounds of peanut butter are sold
each year in the U.S., and peanut butter and jelly is the most popular
sandwich among children. Peter Pan is one of the nation's top three brands,
though well behind market leader Jif. Great Value peanut butter is also
produced by some other manufacturers for Wal-Mart.
In a measure of peanut butter's popularity, ConAgra's hot
line was swamped with so many calls after the recall was announced on
Wednesday that many people got a busy signal. School officials in Houston
confiscated students' sandwiches from home and replaced them with those made
at schools. And in Georgia, a lawmaker representing one of the nation's
biggest peanut-producing areas warned colleagues to throw out jars of peanut
butter that he recently handed out.
The outbreak was detected by the CDC and state health
agencies when they noticed spikes in the cases of people sickened by an
unusual type of salmonella, starting in August. Once peanut butter emerged
as a link, the CDC notified the FDA.
Salmonella commonly originates in the feces of birds and
animals, and could be introduced at a multitude of stages in the peanut
butter-making process. But many safeguards are in place.
While rodents and birds commonly get into peanut storage
bins, germs are killed when raw peanuts are roasted. When making peanut
butter, the nuts are again heated — above the salmonella-killing temperature
of 165 degrees — as they are ground into a paste and mixed with other
ingredients before being squirted into jars and quickly sealed.
"The heating process is sufficient to kill salmonella,
should it be present," said Mike Doyle (news, bio, voting record), director
of the University of Georgia's Center for Food Safety, in the state that
produces nearly half of the nation's peanuts.
Experts say the point in the process where salmonella could
be introduced and survive would be as the product cools down, is placed in
the jars and then sealed. At most plants, those steps take just minutes.
But "there is quite a lot that happens after that heat step
... before it's put in jars. So there's definitely an opportunity for
contamination after the roasting," the FDA's Acheson said.
Acheson speculated a small, on-again, off-again source of
contamination caused the outbreak, which would explain the relatively small
number of illness. That "will make finding it in peanut butter difficult.
But that's not going to stop us from looking," he said.
Other states reporting cases are Alaska, Alabama, Arkansas,
Arizona, California, Colorado, Connecticut, Georgia, Iowa, Illinois,
Indiana, Kansas, Kentucky, Massachusetts, Maryland, Maine, Michigan,
Minnesota, Mississippi, Montana, North Carolina, Nebraska, New Jersey, New
Mexico, Ohio, Oklahoma, Oregon, South Carolina, South Dakota, Texas,
Vermont, Washington, Wisconsin and West Virginia.
The strain in this outbreak, Salmonella serotype Tennessee,
is comparatively rare, as is salmonella contamination of peanut products,
said Caroline Smith DeWaal, director of food safety at the Center for
Science in the Public Interest.
"It's taken them a
long time to identify peanut butter as the cause, but that may be because
they had to get over their denial. It's just not one of the first things
you'd suspect," Smith DeWaal said.
___
To get a refund,
consumers should send lids and their names and addresses to ConAgra Foods,
P.O. Box 57078, Irvine, CA 92619-7078. For more information, call (866)
344-6970.
___
Associated Press
Writers Andrew Bridges in Washington, Josh Funk in Omaha, Neb., and Elliott
Minor in Butler, Ga., contributed to this report.
___
On the Net:
http://www.conagrafoods.com

FDA: Rotavirus vaccine may harm infants

By ANDREW BRIDGES,
Associated Press WriterTue Feb 13, 11:14 PM ET
The government
warned on Tuesday of potentially life-threatening twisting of the intestines
in infants vaccinated against a virus that is the leading cause of early
childhood diarrhea. The condition, called intussusception, is the same that
led to the withdrawal of the first rotavirus vaccine eight years ago.
The Food and Drug
Administration said it was unknown whether the recently approved vaccine,
called RotaTeq, caused the 28 new cases. The condition also can occur
spontaneously. Indeed, the reports don't exceed the numbers expected to
occur naturally each year — the so-called background rate, the FDA said.
"It looks like this
is the natural background rate that we are seeing," said Dr. Michelle Goveia,
medical director for pediatric medical affairs at the vaccine's
manufacturer, Merck & Co. Inc. Goveia suggested heightened concerns about
the previous vaccine, made by Wyeth, prompted the FDA to act.
In Tuesday's public
health notification, the agency said it wanted in part to encourage
reporting of any additional cases of intestinal twisting or blockage to help
it assess any risks associated with the three-shot vaccine series. It also
said the vaccine's label would mention the cases of intussusception.
"It's a known
serious, life-threatening adverse event that is being seen at an expected
level postmarketing. But because it is so serious, we asked the company to
change the label," FDA spokeswoman Karen Riley said.
Dr. Paul Offit, the
vaccine's co-inventor, said the 28 reports were well below the hundreds of
cases one would expect naturally. He suggested the FDA wanted to "shake the
tree" for more reports about the vaccine.
"I am actually
encouraged by those data: 28 cases, when you would have expected at least
500 cases, that is really reassuring," said Offit, of the Children's
Hospital of Philadelphia. "I don't see how those numbers suggest something's
awry. If anything, they suggest nothing's awry."
The 28 cases
included 16 infants who required intestinal surgery. There have been no
reports of deaths.
RotaTeq received FDA
approval in February 2006. At the time, the FDA and Merck said trials of the
vaccine involving nearly 70,000 infants indicated it did not increase the
risk of intussusception. But Merck and the Centers for Disease Control and
Prevention are conducting follow-up studies of tens of thousands more
infants to track any long-term effects of the vaccine. The FDA also is
monitoring reports.
About 3.5 million
doses of the Merck vaccine have been distributed in the U.S., though not all
have been used, the FDA said.
The earlier
rotavirus vaccine, Wyeth's RotaShield, was pulled from the U.S. market in
1999 after it was linked to a small increase in intussusception. It had been
on the market a year.
In the United
States, rotavirus sickens about 2.7 million children younger than 5, sends
up to 70,000 to the hospital and causes 20 to 70 deaths each year.
___
On the Net:
Food and Drug
Administration notification on RotaTeq: http://www.fda.gov/cber/safety/phnrota021307.
htm

FDA restricts use of
antibiotic
The government on
Monday restricted an antibiotic linked to rare reports of severe liver
problems including several deaths, saying the drug should be used only to
treat pneumonia and not less serious illnesses.
The Food and Drug
Administration said the antibiotic, Ketek, would remain on the market but
that its label will bear a new, stern warning. The agency said it and
manufacturer Sanofi-Aventis SA also created a guide for patients outlining
the drug's risks and its safe use.
The FDA announced
the changes on the eve of a House subcommittee hearing on drug safety that
will examine irregularities in the approval of Ketek.
FDA spokeswoman
Susan Cruzan said Monday's announcement was not timed to coincide with the
hearing. One member of Congress questioned that.
"It appears that a
healthy dose of congressional oversight has reminded them to do their job
and ensure the safety of drugs on the market," said Rep. Edward Markey
(news, bio, voting record), D-Mass.
The changes are in
line with the December recommendations of a panel of FDA expert advisers
that the agency modify the label of the drug, also called telithromycin. In
17-2 votes, the outside advisers said the drug's benefits don't outweigh its
risks in treating bronchitis and sinusitis, which are less serious
infections than pneumonia and often spontaneously resolve on their own.
"The agency has
determined that the balance of benefits and risks no longer support approval
of the drug for these indications," the FDA said in a statement.
The FDA's handling
of the antibiotic remains under investigation by the Senate as well.
"The FDA's action
today shows what transparency can do. When a spotlight was turned on the
questionable way in which Ketek got approved by the FDA for certain sinus
and lung infections, the FDA was held accountable," said Sen. Charles
Grassley (news, bio, voting record), R-Iowa, long a critic of the FDA's
handling of Ketek.
A new so-called
"black-box" warning on the Ketek label states the drug should not be used in
patients with myasthenia gravis, a disease that can cause life-threatening
muscle weakness, the FDA said. The label also now warns about cases of
visual disturbances and loss of consciousness reported in some patients.
The label already
warned of the drug's risk to the liver. An FDA review released in December
cited 13 reports of liver failure in patients treated with the drug. The FDA
has since learned of one additional such case.
As of late last
year, doctors had prescribed the antibiotic more than 5.6 million times in
the United States since it won FDA approval in 2004.
"Ketek, when used as
directed in its approved indication, continues to be an important option"
for fighting infections and "helps to satisfy a medical need," Sanofi-Aventis
said in a statement.

Following From:
January 18, 2007
NEW: Fluoridation
Warning Issued for Infants
See also:
TAKE ACTION!
Ask Wal-Mart to Stop
Selling Fluoride Water to Infants

Bacteria-Eating Virus Approved as Food Additive
(are
you kidding me?!?)
FDA Approves Controversial Spray-On
Viruses For Deli Meats

Jimmy Moore
August 21, 2006
The following is a reprint from
the blog
"Living La Vida Lo-Carb"
That low-carb deli meat you enjoy will soon
contain something more!
Whenever you hear the U.S. Food and Drug
Association (FDA) place their seal of approval on something to be included in
our food, generally you feel pretty confident that the newly-approved food
additive is safe for consumption. But have you seen what they just approved to
be sprayed on deli meats that are a popular food choice for people who are livin'
la vida low-carb?
This
Forbes story reveals the shocking news that the FDA is going
to allow for the very first time a series of six viruses to be sprayed as a food
additive onto deli meats such as sliced turkey and ham as well as hot dogs,
sausages, and other ready-to-eat packaged meats. You heard me right--VIRUSES
SPRAYED ON OUR MEAT!
Before I get into the story, what do you think
about that? My gut reaction was immediately, "Oh my gosh, what are they going to
be putting on our meat now?!" It freaked me out worse than finding out
how chargrilled chicken served in popular restaurants is really made!
Unlike
probiotic foods which put good bacteria in your body to
combat the bacteria that would cause you to get sick, this is different because
you won't have a choice about whether you consume this or not. It's FDA
mandated.
Plus, what is the sudden urgency of this that
would cause the FDA to move so quickly to grant approval for this virus
concoction to be put on perfectly good meat? Well, it appears there is a segment
of our population that gets sick with an infection called
listeriosis and one-fifth of those people die annually. How
many Americans contract listeriosis each year and get sick and/or die? Millions?
Hundreds of thousands?
Would you believe ONLY 2,500 get seriously ill
and a grand total of 500 of those people die, according to statistics from the
U.S. Centers for Disease Control? That's a mere SEVEN people for every one
million who get the disease and just a little over 1 person per million who
dies. That's it! And THIS warrants a move to introduce a series of viruses to
tens of millions of people?! ARGH!
While it is awful to hear that ANYONE has to get
sick or even die from something as horrific as something like listeriosis, does
it really take a drastic action by the FDA like spray-on viruses on deli meats
when the overwhelming majority of Americans will not be affected by this
disease? Who's to say these new viruses won't lead to some other kind of
sickness in the millions upon millions of people who would otherwise be just
fine eating the meat sans the viruses? There are too many unanswered questions
in my mind to make me feel comfortable with this.
The story explains that this virus spray
developed by a company called
Intralytix, Inc. (who stands to reap HUGE profits from the
sale and distribution of their virus spray) is actually
bacteriophages which fight and kill the Listeria
monocytogenes bacterium that ends up on uncooked deli meats. This disease is
more apt to hit women who are pregnant, newborn babies and adults with a weak
immune system.
So, if those people are in the high-risk
category, then why don't we give them access to this virus spray so they can
give a little squirt on their meat before eating it if they are the ones who are
most susceptible? Why expose the other 99.999% of us who don't have any
difficulty eating deli meats to this new string of viruses that may or may not
be good for us to consume over the long-term? By the way, where are the studies
on how safe these viruses really are? Hmmmm? FDA, it's time to pony up the
information!
I eat a lot of sliced turkey as part of my low-carb
lifestyle. I really enjoy eating a cold cut turkey and cheese wrap with a little
mayonnaise and/or mustard and sometimes some spinach leaves. It's a quick and
easy lunch and helps fuel my workout during my lunch break from work. I have
eaten it hot out of the microwave and cold, so I guess I have been exposed to
the risk of getting listeriosis myself. But I have eaten luncheon meats 5 days a
week for the past three years with no sign of sickness at all. NONE!
But now I'm going to be exposed to these viruses
which will make me rethink the kind of meats I buy from the grocery store. This
really stinks, ya know? Sure, Intralytix President and CEO
John D. Vazzana, who has been lobbying the FDA to approve
their virus spray since 2002, says this food additive (as they are calling it)
is completely safe as does the FDA food additive safety regulator Andrew Zajac.
"As long as it used in accordance with the
regulations, we have concluded it's safe," Zajac said.
But what makes them so sure the viruses will be
used "in accordance with the regulations" and not cause people any harm? Oh,
we're just supposed to trust them and believe them at face value that these
supposedly "safe" viruses they are adding to our food will have ZERO negative
impact on our bodies. Puh-leez! I wouldn't trust the government from here to my
front door on something that could directly impact my life like this.
Here's a scary quote from the
FDA:
"The viruses are grown in a preparation of the very bacteria they kill, and
then purified. The FDA had concerns that the virus preparation potentially could
contain toxic residues associated with the bacteria. However, testing did not
reveal the presence of such residues, which in small quantities likely wouldn't
cause health problems anyway," the FDA said.
Jeepers creepers! Since listeria exists in deli
meats primarily because they are not cooked or heated up prior to consumption,
then why doesn't the FDA just put out a recommendation for people in the
vulnerable groups to do just that prior to consuming these foods? That certainly
makes a lot more sense than taking the bold and risky action to begin spraying
viruses on the meat that millions of people consume daily. Duh!
Even scarier is the eerie revelation by Zajac in
this story that consumers will
have no idea this virus spray has been added
to the deli meats they purchase. If it's so safe, then why not? Yikes, you mean
there won't be a big yellow sticker on it with the message "FDA-APPROVED
SPRAY-ON VIRUSES APPLIED TO THIS MEAT!" Ya think Oscar Meyer and Bryan would
appreciate having that on their bestselling deli meats? Nah, didn't think so.
UGH! Do you see where this is going people? Now
that the FDA has approved this action, Intralytix is already feeling cocky
enough to begin an immediate worldwide production of their spray-on virus and
are even currently working on another spray that will allegedly kill the E. coli
bacteria on beef prior to grounding. AAACK! What are they doing to our beef
now?!
Are you as outraged about this as I am? If not,
then you should be. Feel free to tell me why you aren't angry about this if this
is of no concern to you. But if you are upset and want to voice your opinion,
then make your voice heard by commenting below and also by demanding answers
from Andrew Zajac at the FDA. E-mail him to express YOUR concerns about this
issue at
andrew.zajac@fda.hhs.gov. Let me know if he responds so I
can post it here.
This is an important issue for people who are
livin' la vida low-carb and I urge you to tell everyone you know about what the
FDA has approved to be put on deli meats. MAKE A FUSS, SAY NO TO VIRUS!

FDA APPROVES VIRAL ADULTERATION OF OUR FOOD SUPPLY
By Byron J. Richards,
CCN

August
24, 2006
www.NewsWithViews.com
On
Friday, August 18, 2006, the
FDA approved a viral cocktail to be
sprayed on foods we eat. This is the first time viruses have been approved for
use as food additives. The FDA wants you to believe it will be safe to consume
these viruses every day for the rest of your life with no adverse health
effects. Not surprisingly, the FDA doesn’t want you to know which foods are
adulterated in this manner, for fear you may not buy them; thus, no labeling
will be required. This is a monumental announcement by the FDA, indicating they
are throwing all caution to the wind regarding the safety of our food supply.
Are you
willing to stand in line for a virus-laden sandwich? How do you like the idea of
buying virus-infested food for your family? The first virally contaminated foods
entering our food supply with the blessings of the FDA will be luncheon meat and
poultry. Live viruses will be sprayed on foods such as cold cuts, sausages, hot
dogs, sliced turkey, and chicken.
At issue
is the very real problem of a poor quality FDA-approved food supply that is
already full of diseased and sickly animals, many of them imported from other
countries. The use of antibiotics during growth and radiation during food
processing is required by the fast-food animal farms owned by multi-national
companies to cover up the horrendous health of the animals they wish to feed to
Americans. Animals in poor health are a friendly place for bacteria to grow and
prosper, especially after such meat goes to market. Rather than address the
source of the problem, the FDA wants to add another adulteration into our food
supply.
The
stated goal of the new FDA-approved viruses is to kill a rare bacterium known as
Listeria monocytogenes. This bacterium is killed by cooking; however, it poses a
problem in meats that are cooked during processing and not cooked again prior to
consumption, so it can readily infect foods such as deli meats.
Yes, the
FDA plans to use one infectious organism to fight another. The carnage of battle
will end up in your digestive tract along with the victorious live viruses,
which the FDA assures us will not attack human cells. However, they cannot
possibly be certain the viruses will not attack the friendly bacteria that make
up the lining of your digestive tract. And they want you to believe this is
completely safe while refusing to require the additive viruses to be listed on
the food label so that you would have a choice.
Turning Loose the Bacteria-Killing Viruses
The
company that produces these biotech viruses is Baltimore-based
Intralytix, Inc.
The viruses are known as bacteriophages, viruses that kill bacteria, or phages
for short. Phages have been around a long time, living as parasites inside many
bacteria.
Intralytix uses biotechnology to grow viral phages in a culture with Listeria,
in theory teaching the viruses to recognize the bacteria. The FDA-approved
cocktail contains six different viruses intended to attack one strain of
bacteria.
This
concoction is then sprayed on food. If Listeria is present in the food, the
bacteria will ingest the viruses. This results in massive viral replication
inside the bacteria, until such point as the bacteria simply bursts. This battle
results in significant production of bacterial poisons called “endotoxins”, as
the bacteria tries to defend itself. When the bacteria burst, these endotoxins
are released. These, along with the victorious live viruses, will now be on the
food that will be eaten.
The FDA
and Intralytix would like us to believe that these viruses will only attack the
specified bacteria they are intended to kill and will be harmless to humans. I’m
sorry to burst their bubble, but they can’t possibly guarantee such safety. It
is true that the viruses, at least at this time, cannot recognize human cells.
However, the virus can potentially recognize normal bacterial cells in the human
digestive tract and may be able to adapt to infect one or more of these friendly
bacteria.
The
FDA Certainly Knows There Are Risks
The FDA
had some concerns about the amount of bacterial endotoxin in the Intralytix
product before it is sprayed; however, FDA tests apparently showed that the
product was adequately purified and so they declared it safe if used as
approved. Will the FDA diligently monitor the quality of this product once it is
on the market, or will it go the path of many FDA-approved drugs that the agency
can’t keep track of?
There is
certainly a risk that humans will be exposed to excessive amounts of endotoxin.
This could come from the manufacturing of the viral cocktail, the interaction of
the viruses with bacteria after being sprayed on food, and/or the interaction of
the viruses with bacteria in the digestive tract.
The human
immune system is highly reactive and sensitive to bacterial endotoxins. They
provoke allergy, asthma, autoimmune problems, and elevate cholesterol. They also
interfere with the healthy function of
cells lining the digestive tract.
Researchers have demonstrated that the presence of
bacterial endotoxins can start cancer in the colon.
Additionally, the human immune system reacts directly to viral phages. Thus, a
person who eats a lot of processed deli meat is certain to evoke an immune
reaction to the viruses. What will this reaction be? Allergy? Asthma?
Autoimmunity? Cancer? How can the FDA approve a food additive that it knows can
induce a variety of human immune responses? Phages are so good at disrupting
normal immunity that they are being considered for use as part of
organ transplant medicine.
The
ingestion of significant amounts of viral phages into the human digestive tract
is a wild card full of unknown outcomes. For example, it is certainly possible
that these phages, which constantly mutate in order to survive, are likely to
find a way to infect bacteria they were not intended to infect. Since phages are
parasites, they could hijack the friendly bacteria of the digestive tract and
turn them into viral machines, constantly generating viral particles that are
likely to confuse the human immune system, if not directly infect the body. We
know from history that these viral phages can turn innocuous bacteria into a
killer, which is how cholera occurs.
Furthermore, the Listeria bacteria are not going to take the issue lying down.
They will develop resistance to the viruses over time, as we have seen with the
overuse of antibiotics. Going down this path we are likely to have hundreds of
viral food additives in the food we eat, all designed to combat some possible
infection coming from poor quality food. Sooner or later we will inadvertently
create deadly new super-strains of bacteria and/or parasitically infect the
human digestive tract with an untreatable infection.
There is
also the very real possibility of unintended viral recombination. What happens
when a person with viral stomach flu eats food containing a dose of this viral
food additive? It is certainly possible for the genetic material of the flu
virus to interact with the genetic material of the viral phages, provoking an
undesirable new viral infection.
Let’s not
forget that the FDA won’t tell us which foods in the food supply contain
genetically modified organisms (GMO). Seventy percent of the packaged food on
grocery shelves already contains GMO adulterated food. These foods have viral
promoter genes woven into the DNA of every cell, a technique used to implant a
pesticide toxin into every cell of this fake food (see
Fight for Your Health, chapter 15). What
happens when the viral phages interact with the viral promoter genes in GMO
food? What new virus will be encouraged to form?
Keep in
mind that the FDA wants to conduct this experiment on our food supply to protect
a small minority, only about 2500 people, who are made seriously ill by this
infection each year. The ill are mostly pregnant women, elderly with compromised
immunity, and small children. It would be a lot more to the point if the FDA
would simply warn such people that eating these foods, due to their poor quality
of production, may be dangerous. What the FDA should really do is improve the
quality of our food supply, the true source of the problem. Why expose millions
of Americans to an unproven ingestion of live viruses for the benefit of so few?
The FDA
has failed miserably for the past century to protect the public from the
adulteration of our food supply by vested interests. This is just one more
insult added to a long list of injuries.
The
Tip of an Iceberg
Intralytix has an agenda for the American food supply, as well as for healthcare
in general. This recent FDA ruling allows Intralytix and other similar biotech
companies to get their foot in a door that should be slammed shut and bolted
closed.
The
company is also seeking FDA approval for viral sprays to treat foods that could
be contaminated with E. coli and Salmonella, which means that similar “trained”
viruses could end up in a majority of the protein foods in our food supply.
Intralytix sees financial opportunity. They have already licensed their now
FDA-approved viral spray to an undisclosed multi-national company for use around
the world. When the CEO of Intralytix, John Vazzara, was recently asked about
this partner company,
he refused to disclose their name. The
grand profit-driven biotech experiment on the health and well being of all
Americans is now in full swing.
Of
course, we will need new wonder drugs to combat the new bio-tech produced
infections. Americans will stay sick and the sickness-driven bio-tech industry
will flourish. The bio-tech industry will make people sick on the front end and
treat them on the back end. It’s a win-win situation for profit on illness.
The
FDA is Rapidly Becoming a Public Enemy
Experimenting with viruses being added to the food supply is incredibly
dangerous and reckless. It is completely impossible for the FDA to guarantee
safety in the near term or the long term. Thus, the FDA has made the
bureaucratic decision that relative safety is acceptable to them. What right
does the FDA have to tamper with the food supply in this manner?
It is
quite clear that the Bush agenda has been to promote American biotech companies
as the new future for American prosperity. Administrative opinions have trumped
science in virtually every situation wherein safety conflicts with profit.
The FDA
will refuse to require labeling on food sprayed with viruses, just as they
refuse to require notification that food has been genetically modified and
contains toxins in every cell. The reason is obvious; no person understanding
these issues would buy or eat such food. Thus, the FDA acts to hide the
information from the public to foster profits for biotech companies and the
growth of the biotech industry. This is a betrayal of the public trust.
The
leaders of the FDA are personally responsible and need to be held accountable.
This means Andrew von Eschenbach, M.D., temporary head of the FDA and his chief
science officer, Scott Gottlieb, M.D. These men are not only
obsessed with approving risky drugs for
the benefits of Big Pharma, it is now clear that they are willing to allow
obvious adulteration of the food supply. They seek to control what we eat, and
they are tampering with survival of the human race.
The FDA
does not truly know how safe viral phages are to consume on a regular basis.
They have no idea of the cumulative effect over the course of a lifetime,
especially as more of these viral cocktails are added to the food supply. They
have no way to measure how this new type of adulteration in the food supply will
interact with the poor digestive/immune health of half the American population,
in combination with all the other serious adulterations already approved by the
FDA. The FDA lacks due diligence in honoring its mandate to protect the American
public.
Boycott Viral Tainted Foods, Support Your Sustainable Farmers
The only
hope Americans have is to resurrect the quality of our food supply. Doing so is
against the odds, as there are billions of dollars of profit-mongering taking
our food supply in the wrong direction. One day Americans will realize that food
security is as important to national security as any other topic. It is now
crystal clear that we cannot count on the FDA to do the job that Harvey Wiley,
M.D.,
envisioned one-hundred years ago.

'Every Link of the Food
Chain Affected' a New Report Says
By LAURA MARQUEZ
Sept. 18, 2006
— - Mercury contamination is making its way into nearly every habitat
in the United States, not just oceans, according to a report that the National
Wildlife Federation will release Tuesday.
The problem with high
mercury levels in certain types of fish has been well documented, resulting in
46 states issuing advisories for pregnant women and children to avoid eating
certain types of fish, including tuna and swordfish. High levels of mercury
can lead to a wide range of physical ills, including kidney and neurological
damage, and can cause fatigue, vision problems and tremors.
But this is the first
report to expose the problem in such a wide variety of species, 40 to be
exact.
The report
"underscored how pervasive mercury contamination has become," according to
Felice Stadler at the National Wildlife Federation. "Nearly every aspect of
our food web has been contaminated. It's difficult to find an ecosystem that's
not contaminated, whether it's ocean or forest or coastal waters or wetlands."
Scientists found high
levels of mercury in bald eagles, songbirds, polar bears and alligators, to
name just a few species. Alligator meat is very popular in the southeast, but
there is no advisory against eating alligator meat.
Last year Utah issued
an advisory for duck hunters, warning people to limit or avoid eating certain
duck species because of high levels of mercury.
Stadler said this
report "raises the question of what ecosystems are safe and immune from toxic
contamination."
Mercury is a naturally
occurring element, but people release much more mercury pollution that ends up
in our forests, lakes, and streams -- 100 tons in this country alone annually.
The primary sources include coal-burning power plants, wastewater treatment
plants and waste incinerators.
The mercury pollution
is affecting the reproduction and behavior of fish and wildlife. The report's
findings suggest birds with high levels of mercury lay fewer eggs, and the
motor skills of certain mammals have been diminished, which affects their
ability to hunt and therefore survive.
The report points out
"there truly is no link in the food chain untouched by mercury," and according
to Stadler, this carries broad implications for humans.
"The research shows
birds that eat contaminated insects get contaminated themselves," Stadler
said. "Turkeys and chickens, which humans eat, eat those same contaminated
insects, so this is the tip of the iceberg."
There is some good news in an otherwise glum report: Mercury
poisoning is reversible.
Stadler pointed to
several states that in recent years have taken steps to cut mercury emissions,
including Florida, Wisconsin, New Hampshire and Massachusetts.
And in a much shorter
time than expected, the mercury levels in those states' fish and wildlife
populations have dropped
Stadler, who's been
working on the issue of mercury pollution for 10 years, said she was
originally told it would take 50 years before scientists would see some
reversal.
"But it's happening
much faster than we ever thought, five to six years," she said.
Stadler said she
believes the key is for this country -- and the whole world for that matter --
to realize just how big a threat mercury pollution is to our ecosystems.
"We need to be as
drastic at cutting mercury as we have been in cutting lead," she said.

What is Iatrogenocide?!
As many as 98,000 Americans die
in Hospitals each year of preventable medical errors. One million more are
injured. In fact, medical errors kill as many people per year as Breast
Cancer, HIV-AIDS and car accidents.
From the March 2002 Idaho
Observer:
Quarter-million doctor-induced
deaths annually: Iatrogenocide?
IATROGENIC [Gk., iatros, physician, genein, to produce],
caused by treatment or diagnostic procedures. An iatrogenic disorder is a
condition caused by medical personnel or procedures or through exposure to
the environment of a health care facility, including fears instilled in
patients by remarks or questions of examining physicians. See also: 'nosocomial',
(iatrogenesis, iatrogeny, n.) ~Mosby's Medical Dictionary, 5th Edition, 1998
by Alan Yurko
It is well known that many new
drugs, devices, surgeries and treatments are touted as miracles of modern
medicine. However, there are two sides, possibly two hundred sides to such
claims. This article focuses on a dark side. Caveat Emptor: Buyer Beware.
Ninety-five percent of the
people I know are doctors, scientists or activists in health care issues
and/or victims of iatrogeny -- including myself. They have commanded my
honor and respect since many of these people are addressing epidemic
iatrogeny in their work.
A generation ago, people
trusted their doctors blindly and implicitly. The personal bonds people used
to form with their doctors have largely been replaced with the cold hard
contemporary reality that medicine has become a $multi-billion per year
business with little room for compassion. The healthcare market place is not
kind and people have lost trust. Iatrogeny plays a large and ugly role in
this.
A recent study published in The
Journal of The American Medical Association (2000:284:94) by Barbara
Starfield, MD, MPH, showed that in the U.S. there are:
* 12,000 deaths/year from
unnecessary surgery
* 7,000 deaths/year from
medication errors in hospitals
* 20,000 deaths/year from other
errors in hospitals
* 80,000 deaths/year from
nosocomial infections in hospitals
* 106,000 deaths/year from
adverse effects of medications
This totals 225,000 deaths per
year from iatrogenic causes, placing iatrogeny as the third leading cause of
death in the U.S., second only to heart disease and cancer. The scary part
is that this does not include disabilities and disorders; just deaths in
hospitalized patients. In any event, when one ponders that more than four
times as many people die in one year from doctors' mistakes than died in the
entire Vietnam War, one is aghast at why this information isn't making
headlines or why huge think tanks funded by medicopolitical interests
haven't formed.
We have the American Heart
Association to address heart disease, Richard Nixon's “War on Cancer,” and
even groups like “Mothers Against Drunk Driving.” Organizations have been
formed to address almost every sort of issue, save iatrogeny.
My guess is that medicopolitics
have not figured out a way to capitalize on of all these deaths and
disorders, ... yet. There is, however, a small “experts” consortium that
does address iatrogeny in the journals, but such studies are few and far
between. Funding such studies doesn't appear to be sound business practice.
Iatrogeny is not exclusive to
the U.S. The British Medical Journal stated March 18, 2000 that, “In
Australia, medical error results is as many as 18,000 unnecessary deaths,
and more than 50,000 patients become disabled every year.”
Studies released in the last 10
years show similar trends in the UK, Canada and New Zealand. New Zealand has
a large percentage ratio of adverse drug reactions comparable to the U.S. It
should be noted that the U.S. and New Zealand are the only countries that
allow aggressive pharmaceutical drug advertisements.
One very interesting statistic
are deaths attributed to addictive drugs in the UK between 1990 and 1995:
Benzodiazepines - 1,810
Methadone - 676
Heroin - 291
This emphasizes my point that
millions of dollars are given to organizations for deaths and disabilities
from a myriad of causes, except iatrogeny. Here we have two legal
prescription drugs causing more deaths each, than heroin.
Many can pooh-pooh these
statistics and claim that to err is human, etc., however there comes a point
when one must look deeper. The facts and statistics are too overwhelming to
ignore. Those in power have choices to make. They can rationalize, deny or
take responsible action against epidemic iatrogeny.
The latter seems to be slow in
genesis. There has been much denial and silence from the allopathic medical
industrial complex. Since medicine has become an arm of business and since
business and politics are such passionate bedfellows, one must look at some
other interesting facts.
Drug companies spend huge
fortunes for political influence. In fact lobbying for pharmaceutical
interests in the first half of 2000 reached $42.9 million; and it was
estimated that $230 million would be spent during the election. George Bush
welcomed $1.7 million from drug companies just for his inauguration
celebrations (British Medical Journal January 27, 2001).
Drug companies are a business
and have always been a business. They do not give such an investment without
an expected return with profits. Perhaps this is why officials turn a blind
eye to the fact that doctors and hospitals are responsible for nearly a
quarter-million deaths in the U.S. per year. Or perhaps this is why the
pharma-companies manufacture pesticides and chemicals that cause cancer and
disease and then manufacture drugs to treat diseases they cause that can
cause even more disorders to create a market for more drugs -- and more
profit.
The scenario above describes a
very lucrative cycle. Perhaps this is why funding for disease research
successfully diverts attention from the pharmocartels' own carcinogenic and
deadly products. One need not look too hard for reasons why doctors' and
hospitals' mistakes are the third leading cause of death in America -- with
no end in sight.
Many believe that Barbara
Starfield's study cited earlier is just the tip of the iceberg. After all,
the study only looked at hospitalized patients. What of the in home and
outpatient errors? There are more people to consider in these groups, and
certainly more iatrogeny. Could it be that iatrogeny is the leading cause of
death in the U.S.? In the World?
As startling and unsupported as
that sounds, it may very well be true. At any rate, the iatrogenic holocaust
makes World War II deaths pale in comparison. Yet only patronizing and
minimal attempts to recognize and correct iatrogeny have been made.
Murder Or Mistake?
The fine line between murder or
mistake is a hot potato. If you saw your neighbors being killed one by one
or en masse, yet did nothing about it, or took up for the killers, you could
be guilty of “accessory to murder” or “accessory to murder after the fact.”
Many analogies and ethical juxtapositions could be generated in such a
debate. One could even make the argument for a global elitist plan at
population control allowing iatrogeny to gain such momentum.
Regardless of etiology,
iatrogeny is real. It is rampant and far from being under control. By making
iatrogeny, through semantics, sound as if it is an infectious disease beyond
the control of physicians and hospitals, we allow the medical profession and
pharmaceutical cartels to distance themselves from responsibility and
relieve them from the culpability for what mirrors negligent homicide.
It would be humanly impossible
to eliminate genuine mistakes entirely. “But how many times does a mistake
happen until it's not just a mistake anymore, but negligence?”
This author believes that
225,000 deaths every year may be an example of when mistakes cross over to
the darkness of negligence. If so, then we are witnessing the greatest
holocaust to befall mankind ever.
In closing, I leave you with my
own definition of a freshly coined word:
Iatrogenocide - [Gk, iatros,
physician, genein, to produce, cide, killing] The extermination of a
population in a systematic fashion through medical error.
* For more information on
iatrogeny, contact me at
freeyurko@bizland.com
Originally published in The
Journal of Degenerative Disease, February/March 2002: 3(3rd); pages 37-38
The Idaho Observer
P.O. Box 457
Spirit Lake, Idaho 83869
Phone: 208-255-2307
Email:
observer@coldreams.com
Web:
http://idaho-observer.com
http://proliberty.com/observer/

Other Forms Of Iatrogeny and Lawlessness
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QUESTION AUTHORITY...
Do I believe that Physicians
are looking to kill intentionally?... OF COURSE NOT! Although, in one
Hospital stay of mine (in a VERY well-known Beverly Hills Hospital!) the
follow |