Natural Solutions Foundation
www.GlobalHealthFreedom.org
http://www.HealthFreedomUSA.org
(This is the online copy of the Health Freedom Action eAlert of April 28, 2009)
Weaponized Vaccine and Pandemic Threats
Index:
Nano Silver
Engineered Pandemic
Weaponized Vaccines
New World Order
Self-Quarantine & 14 Point Checklist
Anti-Virals
Herbs to Use or Avoid
Herbal Remedies
Miscellaneous Remedies
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First, A Word For Our Sponsors: YOU
When the Natural Solutions Foundation shared our analysis of the weaponization of the Avian Flu with you in 2008, we got many hundreds of emails asking us what to do to protect ourselves. We said very clearly that while the weaponized Avian Flu Virus might not react the way other pathogens did, we predicted that it would be killed by contact with Nano Silver, a finely divided type of silver which kills all known disease-causing agents or pathogens and which is sold as a Dietary Supplement in the US. I was very clear that the Avian Flu organism might or might not respond the same way. As it happened, later information let us know that we were correct: Nano silver DOES, indeed, kill the weaponized Avian Flu virus as it kills all known micro-organisms except beneficial ones.
The US government says that people marketing silver products are not allowed to tell you this truthful information. We told you, within our private, opt-in expressive association, of the truth as we see it. To receive information like this is exactly why you opted into our Health Freedom Action eAlert – http://drrimatruthreports.com/?page_id=187. Please be assured, so long as an open and free Internet exists, we will speak truth to power… for you and for all humans who are facing this “time of plague” together.
We anticipate that the protective benefits of Nano Silver will remain true during this absurdly transparent laboratory-created swine flu surging out of Mexico.
After we notified folks about the uses of Nano Silver to protect against disease, even weaponized disease, two things happened:
1. a sudden push to take Nano Silver off the market by the EPA erupted — to which you responded in huge numbers to push back and protect our right to this natural remedy.
2. We got emails thanking us by the thousands about the topic.
When we first mentioned Nano Silver, people wrote to us asking which product I recommend and I freely shared with our followers that we personally use ABL’s Nano Silver, sold under private label at www.Nutronix.com/naturalsolutions called “Silver Biotics”. We spoke extensively with the manufacture (with whom we were already familiar), made arrangements with Nutronix to get the product to you rapidly and passed that information on to you.
In a particularly twisted, bizarre response to our efforts to inform you, some people have even gone so far as to suggest that we are ‘profiteering’ from the pandemic.
Most people wrote to say “Thank you!” — but a few others have written to say that we should not recommend something from which the Foundation receives any benefit!
Um, why not? “Who”, as General Bert often says, “made that rule?”
This Nano Silver product is one in which we believe and which we believe can save your life. We are certainly banking on it to save ours! And, the Foundation also needs support, because our efforts to inform can also save your life. Let’s be frank: times are tough for all not-for-profits, since the economy has taken a carefully orchestrated beating. The Banksters are doing very well, thanks to wholesale plundering of future taxpayers, (Goldman Sachs says it will return the bailout billions rather than cut executive bonuses!) but we little people are bearing the brunt of their misdoings.
The Foundation recommends products and services that we think are of outstanding value and we sometimes make a small percentage of their sale price, when you buy from the sources we recommend. You have the information for free, of course, and, should you choose to make your purchases elsewhere, we do not get any support, but you have the information to use.
Let’s be clear here: whether you buy Nano silver from us or not, it COULD save your life. IF you buy it from Nutronix, a merchant that gives us a percentage of the purchase price, we get support from that sale. Let me reiterate: Neither General Bert nor I take a single penny from this 24/7 engagement with your health freedom. Not one.
These letters remind me of the few, but memorable, people who, as my patients, told me how grateful they were to me for saving their lives but, since I was doing “the Lord’s work”, I had, as a doctor, they would insist, “no right” to make money from their treatment — as though time, knowledge and experience were worthless!
If you are among Natural Solutions Foundation supporters who disseminate our information, donate (http://drrimatruthreports.com/?page_id=189) and makes purchases through our sites (www.Organics4U.org and www.NaturalSolutionsMarketPlace.org) to support the Natural Solutions Foundation, thank you. We could not do it without you.
But if you are among those few who chastise us for looking to the market as a source of support, please think about this: Only children believe that they should simply hold out their hands and get toys and sweeties without giving something back. We give information, analysis, help and support on a continuing basis. And we look forward to your support as we go forward. It’s called a “reciprocal relationship”. It is a necessary relationship if we are going to heal the world, together.
The predicted, or perhaps I should say, “promised” pandemic may very well be upon us. This is, as sure as God made little green apples, a totally man-made event, with a totally man-made pathogen (disease-causing agent). The WHO, US Government and MMD (media of mass deception) have been ramping up, ramping up, ramping up. But there is no honest virologist in the world who can look you in the eye and say that this virus had any chance whatsoever of having self-assembled genes from Eurasian, North American and other Swine Flu, Avian Flu (already weaponized with the genes of the 1918 Pandemic Virus?) and human viruses, sprung, like Venus from the brow of Zeus on April 14 in Mexico City and then, suddenly it has deadly potential around the globe… without a whole lot of help from its friends.
Deadly potential, by the way, is pretty weird here. There is little doubt that the death toll in Mexico is much higher than previously reported. How high we may never really know.
But there is also little doubt that there is no reason to have declared a “Health Emergency” in the US for a disease which has impacted fewer than 20 people and killed none of them. What pandemic? Who pandemic? Could it be that this pandemic is a totally orchestrated event to make sure that there is an excuse for closing down those few liberties and constitutional rights which still exist after the last devastating 8 years? The “left neocons” continuing the process the “right neocons” started?
I was reading an update from a Chinese site yesterday. It stated that the US, with 20 non fatal cases, had declared a “Health Emergency”, The same site noted that there had been a fatal train wreck in a remote part of China and 21 people were dead. I noted with interest that China did not declare a “Train Emergency”.
Bear in mind that once a global pandemic is declared, just as the US assumes supreme dictatorial powers through Patriot I, II, III, BARDA and other legislation, Executive Orders and Homeland Security Directives, and as the States assume similar powers through the Emergency Medical Powers Acts, passed at the urging of the Homeland Security cabal, so the UN will, according to already prearranged agreement, become the supreme political governing force on the planet.
World government, “elected” by a lowly virus… and an engineered one, at that.
Interestingly enough, of course, it was the Angel of Change, Barak Obama, who, along with then Senator Biden, proposed to the US Congress that a head tax be paid by every man, woman and child in the US to support the UN and that the US military be placed under the authority of the UN, that is, of the New World Order.
I would call that change, all right. And I would say that it may be that a non-pandemic Pandemic just might work to get them what they are looking for.
What will it get you?
Vaccinated with a Weaponized Vaccine.
I have the reports of several Mexican doctors who tell us that their colleagues were vaccinated and died. Vaccinated with what, you may ask? Now that is a really good question. Remembering that the CDC claims that it already has a “seed stock” from this virus which first appeared, they say, on April 14 in Mexico, that is pretty good work.
My research says that it takes quite a lot longer to make the seed stock, the purified and characterized virus, from which vaccines can be made.
And then it takes an absolute minimum of 4 months, if you are favored by the vaccine-making gods, to get yourself a vaccine.
Now, that vaccine may or may not provide any ‘immunity’ against the virus or other organism you are hoping it will protect you from.
Again, according to my research, there is literally NO disinterested evidence to suggest that vaccines provide any sort of protection from any sort of disease (I know, this is heresy to the vaccine priests and their followers – sorry, I am compelled to speak the truth as real science tells us). We do know, however, that vaccination damages the immune system in a rather horrific number of ways. Despite the ‘white wash’ and fol-de-roll, that is simply the science of the matter.
So now we have a new virus, clearly man-made, against which doctors in Mexico are being vaccinated within less than 2 weeks of its being discovered. And they are dying, according to our sources.
What does that tell us? To my mind, it tells us that the entire purpose of this exercise is two fold:
(1) to get those vaccines into your body and
(2) to tie down global control of the planet.
There is no way whatsoever that a vaccine, which is specific to a particular organism, can be effective, to the extent that it is ever effective, against another organism. NONE. Even the CDC admitted earlier today that existing flu vaccine supplies were not “effective” against this Swine Flu (according to CNN).
But, what will the vaccines do? Consider what happened in January when Baxter Pharmaceuticals “accidentally” contaminated shipments of seasonal flu vaccines to 18 countries with live Avian Flu virus. If that “mistake” (how did that live virus get into the very secure vaccine factory?) had not been discovered, there would already be an Avian Flu pandemic… so now, that weaponization having failed, we get the Swine Flu “incident…”
For more details about the January incident, see:
http://drrimatruthreports.com/?p=2220
Some commentators have said that this exercise is only that — a dress rehearsal for the “real thing” and they could, of course, be correct. But whether they are correct or not, the game is going forward and it is one in which the official rule book is being written by those who will benefit from the new feudalism.
Can you Spell “New World Order”
Natural Solutions Foundation always provides solutions when we raise problems and issues. Always. And, since we understand that Nano Silver is the most potent, yet safe, nutritional pathogen killer know, we have been recommending for some time now that you need to lay in a good store of Nano Silver for health threats, both natural and man-made. But there are other ways to regulate the immune system, too, and we want to tell you about some of them. We urgently recommend the Nano Silver route (here is the link again: www.Nutronix.com/naturalsolutions). Man does not live by Nano Silver alone:
Many people have been asking us what they can do to feel less helpless in the face of the possible weaponized flu pandemic about which we have been raising the alarm over the past months. While we are watching closely. We are not totally convinced that the current crisis is a true pandemic, despite the fact that the WHO elevated the threat level a few hours ago from “3” o “4”. We are as greatly concerned about the possibility of a weaponized vaccine forced on the public as the real threat. If the choice is between a ‘quarantine center’ (read: concentration camp) and a vaccine containing unknown dangers, and you are forced to receive an alleged vaccination for a pandemic, the first line of defense would be to consider that perhaps such intramuscular shots are a bit like a snake bite and might be treated in a similar fashion. Get the poison out, as a first line of defense. Detoxify! If you have an Infrared Sauna, use it. Drink large amounts of pure water. Use the detoxifying nutrients and herbs you have available to you. Treat the forced vaccination as though it were the assault on your immune system that it surely will be.
I cannot say what will help, but every bit of mercury, aluminum, fluoride, formaldehyde, squalene, aspartame, MSG, Polysorbate 80 and other toxins you can get out of your body, is better than than that same poison in your body.
Here are some links to information that may help you prepare for what may be coming.
From Natural Solutions Foundation last year –
How to Self-Quarantine; Advice from a Public Health Professional:
http://drrimatruthreports.com/?p=752
The above article was exclusively published by Natural Solutions Foundation and includes expert opinions –
(1) Self-Quarantine Memo from a NBC Protection Expert
(2) Fourteen Preparedness Points, and
(3) Other Preparedness Steps
The following articles were provided by two readers. We pass it along without endorsement or commentary since the information is benign and might help support your immune system in reasonable ways. Please note, we do not think this information will replace Nano Silver or other profound strategies, but it might help protect you and your loved ones.
Nano Silver MIGHT be a magic bullet. These other strategies are not, but can be very helpful used together with a good diet free from contaminants and taken in enough quantity to have a substantial impact. Don’t be embarrassed about wearing a face mask… it may soon be the fashion rage!
Your in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.GlobalHealthFreedom.org
www.HealthFreedomUSA.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
PS: My special thanks to our readers for bringing the following articles to my attention. REL
PS#2: Don’t forget, even in dangerous times, we need to continue to educate decision makers about protecting Health Freedom. Please send your message to the President, Congress and state decision makers, in opposition to the pending (sic) “Food Safety” bills that would force the industrialization of agricultural, destroying family farm, natural and home food production — just when our immune systems need wholesome nutrition the most:
http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=27134
http://www.the-health-gazette.com/health-gazette-blog/alternative-medicine/natural-antivirals
“Research suggests certain natural foods may be as effective against virus H5N1
as commercial antivirals.
(PRWEB) May 10, 2006 — A Biology teacher from Australia, named Stephen Jones,
has done extensive research into the H5N1 virus and compiled a list of natural
foods that are effective against it and listed others that are detrimental.
The list may come as a surprise to many people since foods such as spirulina
and echinacea are listed as detrimental. This strange occurrence is largely
due to the fact that the virus is immune to 2 cytokines that the body produces
(TNF-a and IL-6). Cytokines are compounds produced by the body’s immune system
that attack and remove foreign bodies. The problem is that when a foreign body
is immune to certain cytokines, the body sees that its immune response is not
working and tries even harder, which can lead to what is called a cytokine
storm, where the body becomes flooded with these compounds and they eventually
destroy the body itself. Foods such as Echinacea actually stimulate the
production of these specific cytokines; hence consuming it is not a good idea
if one suspects they may have the virus.
During the 1918 Spanish Flu many healthy young people died from cytokine
storms due to their immune systems overreacting. Consuming foods which
suppress the production of cytokines TNF-a and IL-6 and enhance the production
of the ones that actually are effective against the virus will aid the patient
greatly.
Other foods that create mucous in the respiratory tract, such as bananas, are
also listed as detrimental due to the fact that the predominant breeding
ground of the virus is the respiratory tract and another way in which a
patient may suffer is due to the body’s over production of mucous in this
area.
Natural Antivirals
Folk Medicines and Herbs to use and avoid with Bird Flu
Below is a list of foods that are said to contain substances that are natural
antivirals, immune boosters or they decrease cytokines TNF-a and IL-6.
Alternative medications that are most likely to help us during a severe
pandemic:
Garlic (allicin) – Very effective antiviral. Best if fresh (raw) and crushed.
Must be consumed within 1 hour of crushing. Dosage is initially 2 to 3 cloves
per day but later reduce until no body odour occurs. No toxic effects noted.
(Pubmed PMID 9049657)
Vitamin C – Boosts the immune system and is an antiviral by blocking the
enzyme neurominadase. Viruses need neurominadase to reproduce. There are
anecdotal stories of people taking large amounts of Vitamin C (children ½)
surviving the Spanish Flu. Research shows that it may reduce the production of
cytokines TNF-a and IL-6. A study on 470 people involved giving the test group
1000 mg hourly for 6 hours and then 1000 mg 3 times daily after reporting flu
symptoms. Symptoms decreased by 85%. (Pubmed PMID 10543583, 634178, 16169205,
12876306)
Green Tea (possible Tamiflu/Relenza alternative)- Very effective antiviral.
Also decreases the production of the cytokine (catechins) TNF-a. Inhibits
neurominidase. May have antiviral activity that is equal to other antivirals
such as Tamiflu. (Pubmed PMID 16137775)
St Johns Wort (Hypericum) – Very effective antiviral. Also decreases the
production of the cytokine IL-6. Hypericum is an extract from St John’s Wort.
There have been some very successful field trials in commercial flocks
infected with H5N1 in Vietnam. (Pubmed PMID 7857513, 11518071, 11362353,
7857513, 11518071)
Vitamin E – Immune booster. Also decreases the production of the cytokine
TNF-a. (Pubmed PMID 155882360, 10929076) Experiments involved using mice. Very
suitable for immune compromised people, especially the elderly. Effects
enhanced when taken with Vitamin C.
Apple Juice – Antiviral. Fresh apple juice including the pulp and skin has
greater antiviral activity than heated commercial apple juice. More research
is needed. Effectiveness on H5N1 is unknown. (Pubmed PMID 32832, 12452634)
Resveratrol – Antiviral. In addition to inhibiting neuraminidase, Resveratrol
also sends a message to cells to stop manufacturing viruses. This is a proven
antiviral found naturally in red wine, peanuts, mulberries, Japanese Knotwood
root (richest source), raisins and red grapes. Resveratrol supplements are
relatively inexpensive, are more stable than wine and is available in liquid
form for absorption in the mouth. No toxic effects noted. (Pubmed PMID
1583880, 12817628, 15985724)
Scuttellaria (Skullcap) – Antiviral. A herb used as a tea. It has no side
effects and is also a mild tranquillizer. Research suggests neurominidase,
which is a substance needed by the H5N1 virus to reproduce, may be inhibited.
Cranberry Juice – Early research shows that it may be an antiviral, making
viruses less able to invade or multiply. Effectiveness on H5N1 is unknown.
(Pubmed PMID15781126)
Cat’s Claw (Uncaria tomentosa) – Decreases the production of the cytokine
TNF-a. Also boosts immune system. The number of white blood cells was
significantly increased during treatment. No toxicity was noted.
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD=search&DB=pubmed) Active
constituents can be found in the leaves, bark, vine, and roots. Water
extraction from bark used. Children and pregnant women are to avoid. Has a
potentially damaging effect on the DNA of proliferating cells. (cancers,
fetuses, growing children)
Curcumin (Tumeric Spice) – Decreases the production of the cytokine TNF-a.
This is the yellow compound in turmeric spice. Research shows that this may be
very good for preventing a cytokine storm although this is not proven. Must be
taken with food or gastritis or peptic ulcers may occur. Pregnant women and
feeding mothers should avoid this. The medicinal properties of curcurmin
cannot be utilized when used alone due to rapid metabolism in the liver and
intestinal wall. When combined with Piperine found in black pepper the
absorption is increased with no adverse effects. Obtainable from health stores
in tablets, liquid, capsules already combined with piperine. Dosage is 500mg
to 4000mg daily.
Astragalus root (Astragali Radix) – Boosts immune system. (Pubmed
PMID15588652)
Tea tree Steam Inhalation – Reduces the cytokine TNF-a. Add 2 drops of tea
tree oil in a bowl of steaming water. Cover head with a towel and inhale for 5
to 10 minutes. Relieves congestion and fights infection. Its effectiveness is
unknown. (Pubmed PMID 11131302)
The following substances may be best to avoid during a H5N1 pandemic
Elderberry juice (Sambucal) – AVOID – Increases production of cytokines TNF-a
and IL-6. This substance is very effective against the common flu but may not
be desirable for the H5N1 virus. Increases in these cytokines may trigger a
lethal cytokine storm. (Isr Med Journal2002 Nov;4:944-6)
Micro Algae (Chlorella and Spirulina) – AVOID – Increases production of
cytokine TNF-a. (Pubmed PMID 11731916)
Honey – AVOID – Increases production of cytokines TNF-a and IL-6. (Pubmed
PMID12824009)
Chocolate – AVOID – Increases production of cytokines TNF-a and IL-6. (Pubmed
PMID 12885154, PMID 10917928)
Echinacea – AVOID – Increases production of cytokines TNF-a and IL-6. Although
it is often used for normal flu, research shows that it may increase the
chance of cytokine storms for H5N1. (Pubmed PMID 15556647, 9568541)
Kimchi – AVOID – Increases production of cytokines TNF-a and IL-6. (Pubmed
PMID15630182)
Dairy products & Bananas – AVOID – These foods increase mucous production.
References:
http://www.ncbi.nlm.nih.gov/entrez/ (search using Pubmed ID number listed
after each food)
Natural Antivirals
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Lomatium dissectum root — A Native American remedy. A powerful herbal tincture that kills viruses by disrupting their genes (a chain terminator). When tested at NIH, it made DDI (an AIDS drug) 4000 times more potent. Dose = 2 droppersful / day.
Monolaurin — the natural anti-microbial substance in mother’s milk, made from lauric acid (a fatty acid). Patented by Ecological Formulas. Adult dose is 6 capsules / day. Safe and effective for children at lower doses based on weight.
Echinacea angustifolia root — A native American remedy. Multiple European and American studies have shown that this herb can reduce the risk by one-half of catching a cold, and shorten the duration of a cold by 1.4 days. It should contain all 3 active compounds (polysaccharides, alkylamides and cichoric acid). Dose is 3 grams / day. Not recommended for children.
Olive Leaf Extract — This herbal compound fights bacteria, yeast, fungus and viruses.
L-Lysine — An amino acid that interferes with viral genes (a chain terminator). It has been shown to be extremely effective against Herpes viruses, but has some action against most other viruses.
Vitamin C — Enhances the micro-tubules (cell skeletons) in immune cells, helping them to extend outward (pseudopods) and engulf viruses and bacteria.
Thymus Extract — organic bovine thymus, which provides the 4 basic hormones to stimulate the immune system.
Transfer Factor Plus– A combination of 2 powerful factors: (1) Transfer factors from bovine collostrum, which stimulate the immune system to make natural killer cells. There are over 1000 scientific papers on the efficacy of transfer factor. (2) Japanese mushrooms with anti-viral properties. Together they have been shown to elevate natural killer cells 4000%. Dose 1-2 capsules / day. You can buy Transfer Factor here: http://drrimatruthreports.com/store/cart.php?m=search_results&search=Transfer+Factor&button=Go!
—————————————————–
“April 28, 2009 – Swine flu is a respiratory illness in pigs caused by a virus. Mexico’s
government is ordering closed schools nationwide as the suspected death toll
from swine flu climbed to 149. Health Secretary Jose Angel Cordova says only
20 of the deaths have been confirmed to be from swine flu and the government
was awaiting tests results on the rest. He says 1,995 have been hospitalized
with serious cases of pneumonia since the first case of swine flu was
reported on April 13. Alarmingly, the flu outbreak in Mexico is striking
healthy young people — a pattern that would be expected if a flu virus new
to humans emerged…
Officials in Mexico and the U.S. are taking emergency steps to contain
what is believed to be a new multi-strain swine flu. “If the confirmed
deaths are the first signs of a pandemic, then cases are probably incubating
around the world by now,” said Dr. Michael Osterholm, a pandemic flu expert
at the University of Minnesota. The Mexican Swine Flu has elements of DNA
from the following: avian flu, human flu Type A, human flu Type B, Asian
swine flu, and European swine flu. Human and animal viruses from four or
more continents suddenly recombine in a new flu during a non-flu season that
spreads from human-to-human with a 10% fatality
rating.
Just last month Baxter Pharmaceuticals was caught shipping a mix of H3N2
seasonal flu viruses and unlabelled H5N1 viruses. Baxter released
contaminated flu virus material from a plant in Austria, which contained
live H5N1 avian flu viruses. 2
In Mexico City children rarely use the color blue when they paint the
sky. The atmospheric pollution in the Mexican capital, one of the world’s
biggest cities, is one of the most severe air pollution cases in the world.
Contaminated air hangs over its population of more than 20 million people
doing damage to children’s lungs causing chronic lung diseases when they are
adults. Perched at 7,300 feet in a bowl-shaped valley where the air is thin,
vehicle fumes get trapped and you might as well be living in a gas chamber.
It is that bad and this explains in part why we are finding deaths from the
flu concentrated there with no deaths reported outside of Mexico to this
date. Even the healthy are sick. Full of toxins, they are medically speaking
“accidents waiting to happen,” so when a strong flu strain strikes such a
population the death rate will be very high. The cause of death is
debatable! …
*Infections cannot be separated from the conditions that
invite pathogens to proliferate. This seems to boggle the
minds of orthodox medical scientists, who like the blind men
and the elephant, seem to be able to focus on one thing at a time.*
We live in a dangerous world and anything that throws us out of balance
invites pathogens to take up residence in our bodies. If this is the
beginning of the pandemic that health officials have been warning about it
is best to begin preparing your body before the flu strikes. This article
offers natural emergency medicine that addresses both the body’s terrain and
the potential pathogens quickly. Starting with the most basic medicine, we
need to address dehydration and the use of water and mineral salts as
medicines first.
*Dehydration Dangers*
Complications of flu can include bacterial pneumonia, ear infections,
sinus infections, dehydration, and worsening of chronic medical conditions,
such as congestive heart failure, asthma, or diabetes. Many underestimate
seasonal flu’s severity and neglect treating dehydration, a survey of U.S.
physicians and consumers found. Fifty-seven percent of doctors surveyed said
they considered dehydration the single most dangerous flu side effect.
“Severe flu symptoms like fever and body aches often keep patients from
taking in adequate fluids,” said Dr. Leanne M. Chrisman-Khawam of Case
Western Reserve University in Cleveland. “By managing symptoms, one will be
more likely to manage their dehydration as well.” …
The blood is 80 percent water thus hydration levels are extremely
important in blood chemistry. Moderate dehydration, a 3-5% decrease in body
weight due to fluid loss is sufficient to result in a substantial decrease
in strength and endurance because of the *decrease in oxygen carrying
capacity of the blood signaling a drop in Zeta potential.* Proper hydration
is thus the most basic preventative medicine against death from any type of
flu.
*Mercury Exposure = Increased Vulnerability*
Chronic mercury exposure is also a threat to our health and makes us
especially vulnerable to flu infections. It has been shown that “prolonged
exposure of mammals (white mice) to low mercury concentrations (0.008 – 0.02
mg/m3) leads to a significant increase in the susceptibility of mice to
pathological influenza virus strains. This is shown by more severe course of
infection. In the experimental group more mice died (86 – 90.3 %) than in
the unexposed animals (60.2 – 68 %), additionally the experimental group
died more quickly. The significant difference was in the appearance and
degree of pneumonia in the effected animals,” wrote Dr. I. M. Trakhtenberg
in *Chronic Effects of Mercury on Organisms.*
Though everyone in the northern hemisphere is contaminated with mercury
health officials have a mental block against suggesting anything that might
reduce total mercury body burden. Though some dedicated health activists are
cracking the FDA’s endorsement of mercury dental amalgam it will take a
Martian death ray to get them to protect the public from the obvious.
Natural chelation methods work safely to remove mercury but unfortunately,
if this is the dreaded flu outbreak, there will be little time to reduce
mercury levels. Much can still be accomplished with the emergency protocol
suggested below. Mercury exposure will make flu symptoms worse and even more
dangerous, and that is one reason the flu vaccine is deadly because most
brands include thimerosal, which almost fifty percent mercury.
Several other mercury fighters have a place in the flu battlefield. In
addition to binding mercury into a fairly harmless complex, selenium is a
very good inflammation fighter even in small concentrations. N-acetyl
L-cysteine, an antioxidant and glutathione precursor, stimulates production
of this master antioxidant and, among other things, boosts the immune system
and has anti-inflammatory properties. Alpha-lipoic acid, another mercury
mover, acts as a powerful anti-inflammatory agent, while protecting the
mitochondria and reducing cellular inflammation. Learn about them before you
need them and add them to your medicine kit now.
*Iodine, the Universal Pathogen Killer*
As early as June 1, 1905 an article was printed in the New York Times about the
successful use of iodine for consumption/tuberculosis. Though
iodine kills most pathogens on the skin within 90 seconds, its use as an
antibiotic/antiviral/antifungal has been completely ignored by modern
medicine. Iodine exhibits activity against bacteria, molds, yeasts,
protozoa, and many viruses; indeed, of all antiseptic preparations suitable
for direct use on humans and animals and upon tissues, only iodine is
capable of killing *all classes of pathogens*: gram-positive and
gram-negative bacteria, mycobacteria, fungi, yeasts, viruses and
protozoa. *Most bacteria are killed within 15 to 30 seconds of contact.*
*Iodine is by far the best antibiotic,
antiviral and antiseptic of all time. *
* Dr. David Derry*
Dr. Derry says iodine is effective “for standard pathogens such as
Staphylococcus, but also iodine has the broadest range of action, fewest
side effects and no development of bacterial resistance.” Some doctors have
reported that it is excellent for the treatment of mononucleosis. Iodine
kills single-celled organisms by combining with the amino acids tyrosine or
histidine when exposed to the extracellular environment. All single cells
(pathogens) showing tyrosine on their outer cell membranes are killed
instantly by a simple chemical reaction with iodine that denatures proteins.
Nature and evolution have given us an important mechanism to control
pathogenic life forms, and we should use it and trust it to protect us in
ways that antibiotics cannot.
Dr. David Brownstein, author of *Iodine – Why You Need It,* uses iodine
extensively in his practice and says, “Iodine is a wonderful antibiotic
solution without question and most importantly *I never see any of my
patients complain of dysbiotic reactions from its use.” *Because
drug-resistant micro-organisms continue to emerge and the number of patients
susceptible to these infections is increasing dramatically an approach that
utilizes the innate powers of the immune system as a therapeutic agent will
have the greatest benefit to sick patients. The body’s ability to resist
infection and disease is hindered by long-term deficiency in essential
vitamins and minerals including that of iodine. Poor immune response is
correlated with impaired thyroid function; *a deficiency in iodine can
greatly affect the immune system* because low levels of iodine lead to
problems with the thyroid gland.
I personally talked to a missionary, Stephen Fisher, in Zambia on the
phone last year who told me about his very successful use of iodine to treat
people with malaria. He used 20 drops of Nascent Iodine in a half glass of
water given 4 or 5 times during the first day and then decreased the dose to
10 drops of Nascent Iodine 4 times a day for 3 more days, although higher
dosages can be administered for much longer since iodine is a nutritional
medicine that is needed by the body. Such a protocol can be used for the
swine flu or any other type of influenza. Brownstein and others use much
higher dosages of other iodine forms, namely Lugol’s and Iodoral for cancer treatment.
If you are interested in high dose usage, please read one of the books by
Dr. Brownstein or myself for more details on how to do so.
The minimum number of iodine molecules required to destroy one
bacterium varies with the species. For H. influenzae it was calculated to be
15000 molecules of iodine per cell. When bacteria are treated with iodine,
the inorganic phosphate up-take and oxygen consumption by the cells
immediately ceases. Thus the antiseptic properties of iodine are used to
sterilize every surface and material in hospitals. Iodine is an excellent
microbicide with a broad range of action that includes almost all of the
important health-related microorganisms, such as enteric bacteria, enteric
viruses, bacterial viruses, fungi and protozoan
cysts.
The tremendous diversity and mutability of many infections and their
ability to intelligently exploit the cells is one of the main reasons we
should return to iodine as our favored broad spectrum antibiotic, anti-viral
and anti fungal agent. Iodine provides us with a safe way to strengthen
innate responses to invading microbes while simultaneously correcting or
eliminating a basic nutritional deficiency that causes immunological
unresponsiveness.
*Iodine is able to penetrate quickly
through the cell walls of microorganisms.*
Iodine is a deadly enemy of single cell microorganisms thus it can be
our best friend in our fight against the most dangerous pathogens. Nature
and evolution have given us an important mechanism to control pathogenic
life forms and we should use it and trust it to protect us in ways that
antibiotics can’t.
Dr. David Brownstein, one of a core group of iodine doctors had very
kind words to say about my *Iodine – Bringing Back the Universal Medicine
book.* “Dr. Sircus has done it again. He has written a wonderful book on
iodine that shows the benefits of iodine for treating a wide range of
disorders and how you can incorporate iodine into your daily lifestyle.
This book should be in everyone’s library.” I would say the same about his
book, which inspired my deeper study into the applications of Iodine.
For those who can only get the inexpensive iodine at the drug store meant
for cuts and bruises, know that you can paint the body with it quite heavily
and frequently to get iodine into the body. Just monitor the skin for any
reactions with small area applications first.
*Influenza, Inflammation, and the Role of Magnesium*
What makes avian-derived H5N1 strains, and the influenza strain
underlying the 1918–1919 human pandemic so virulent is viral triggering of
cytokine-mediated lung inflammation. Inflammation is the activation of the
immune system in response to infection, irritation, or injury. Characterized
by an influx of white blood cells, redness, heat, swelling, pain, and
dysfunction of the organs involved, inflammation has different names when it
appears in different parts of the body. Magnesium is central to
immunocompetence, and plays a crucial role in natural and adaptive immunity
in great part because of its dominance over the inflammatory
response.
Magnesium is at the heart of the inflammatory process, it is the prime
first cause when it is not present in sufficient quantities. Increases in
extracellular magnesium concentration cause a decrease in the inflammatory
response while reduction in the extracellular magnesium results in
inflammation. Magnesium literally puts the chill on inflammation especially
when used transdermally. “Magnesium deficiency induces a systemic stress
response by activation of neuro endocrinological pathways,” writes Dr.
Mazur. “Magnesium deficiency contributes to an exaggerated response to
immune stress and oxidative stress is the consequence of the inflammatory
response,” he continued.
A little bit of magnesium chloride can be added to the drinking water
(the same as sodium bicarbonate mentioned in the next section). But both can
be introduced in much greater dosages and concentration in baths to bypass
digestive systems that may not be working properly. Many already know of the
transdermal effect of magnesium chloride and magnesium sulfate. One can also apply both
‘magnesium oil and a self-made lotion of sodium bicarbonate to the skin for rapid
absorption and this is most helpful for children. All can be put into a
sterile solution and nebulized directly into the lungs if inflammation
becomes life threatening. When all else fails, physicians can get both
magnesium and sodium bicarbonate into the body with IVs.
Most people and children are already magnesium deficient, which would
naturally increase complications or the possibility risk of death from
influenza. Everything mentioned in this basic emergency protocol is
preventive and can be started immediately. Don’t wait for the WHO to
officially announce an international pandemic before you stock your
emergency kit with the basics.
*Sodium Bicarbonate*
Using bicarbonate to change blood and full body pH is going to shift
the environment of most pathogens making it more uncomfortable for them to
inhabit a host. Malaria and influenza are often associated with
abnormalities of fluid, electrolytes and the acid-base balance. Sodium
bicarbonate is very useful and should not be overlooked just because it is
one of the most simple medicines and food items you can buy in the
supermarket.
Fluid and electrolyte imbalances easily occur in anybody with a severe
flu. This is common in severe malaria, extremes of age, young children,
malnutrition, and patients with high degree of fever and vomiting/diarrhea.
Sodium bicarbonate can be administered orally every two hours and can
be put in the baths as well as mixed with mineral water to make a lotion.
For oral use, Bob’s Red Mill Sodium Bicarbonate is the best but for baths
the old Arm and Hammer product is fine. Sodium bicarbonate buffers and
defends us from a host of complications, and is even used in chemotherapy to
protect patients from the toxic effects of dangerous drugs.
Sodium bicarbonate along with magnesium chloride are workhorse
medicines that are extremely useful in most all clinical situations.
Certainly they are useful together in infectious diseases to support both
the basic physiology and mitochondrial function.
*Vitamin C*
One does not have to say much when it comes to the importance of
Vitamin C in preparing the body for an aggressive attack of influenza of any
type. If vitamin C levels are low, the body will be more vulnerable to
complications. Also, an attack of the flu will lower already dangerously
depleted vitamin C levels. Whole food vitamin C is often better tolerated
than pure ascorbic acid in addition to the fact that whole food vitamin C
comes with the necessary co-factors for its efficacy, which ascorbic acid
does not.
There are many natural remedies on the market and many wives’s tales
–and there is always Mother’s chicken soup! One will find an extensive list
of possible herbs, formulas and foods that might help; however, they do not
make up a core protocol that one can depend on in an emergency situation
that can easily develop with a severe strain of influenza.
*The Sun – Strong Medicine against the Flu*
Medical scientists have noticed that people with the least D were most
likely to have had a recent infection of the upper respiratory tract. We
already know that getting plenty of vitamin D — more than diet can offer
—
appears to provide potent protection against colds, flu and even pneumonia.
As the amount of vitamin D circulating in blood climbs, risk of upper
respiratory tract infections falls and this is important when strong flu
strains strike hard.
Dr. Adit Ginde, an emergency room physician at the University Of
Colorado Denver School Of Medicine in Aurora says that in people with lung
disease, low levels of the sunshine vitamin “magnify many-fold” the
apparent vulnerability to infection seen in people with healthy lungs. Dr. Ginde
findings appeared in the Feb. 23 Archives of Internal Medicine and concluded
that in every season, people in the lowest vitamin D group were about 36
percent more likely to be suffering a respiratory infection than those in
the highest group.
Grind’s study showed that low levels of vitamin D more than doubled the
risk of respiratory infection for people with COPD — and boosted it almost
six fold in people with asthma — compared with participants who had normal
lung function and were in the highest vitamin D group. What was most
disturbing about the findings was that the NHANES data he analyzed had been
collected about 15 years ago, when almost twice as many people as today had
vitamin D levels above 30 ng/ml. This is a crucial point. We are more
vulnerable today then every before to a massive epidemic because we are more
toxic and more deficient in crucial vitamins and minerals than at any point
in modern history.
One of the most important and misunderstood vitamins is A, and it works
hard to keep you healthy with vitamin D when in the right balance. Vitamin A
plays a vital regulating role in the immune system also. Vitamin A
deficiency leads to a loss of ciliated cells in the lung, an important first
line defense against pathogens. Vitamin A promotes mucin secretion and
microvilli formation by mucosa, including the gastrointestinal tract mucosa.
Vitamin A regulates T-cell production and apoptosis.
If you are a sun lover, you do not need to take supplemental vitamin D;
however you still need to consume adequate vitamin A. Animal studies show
that even moderate amounts of vitamin D increase the body’s need for vitamin
A, whether the vitamin D is provided in the diet or by UV light. So, if you
cut back or eliminate cod liver oil in the summer, you can also consume
plenty of oily fish, liver, butterfat and egg yolks from grass-fed hens to
ensure adequate vitamin A.
So throw away your sun screens and get out in the sun when it is high
in the sky and roast yourself until slightly pink, and do that perhaps every
other day as a replacement for dangerous antiviral medications, along with
the rest of the anti-flu protocol. Drink lots of carrot juice with oranges
and eat spirulina, which is extraordinarily high in beta-carotene.
*In Summary, a Heart Felt Plea*
Please, I beg people to be aware that in November of 2005 Japan’s
health ministry issued a warning of dangerous behavioral side effects linked
to the anti-influenza drug Tamiflu. This came amid reports that several
children in Japan died after taking the medication. Dr. Rokuro Hama, head of
the Japan Institute of Pharmaco-Vigilance, had investigated eight suspicious
deaths of children aged between two and 17, which he thinks are linked to
Tamiflu. He reported his findings at a meeting of the Japan Society of
Pediatric Infectious Diseases. Investigators say in one case last year, a
17-year-old boy, after taking the medication, left his home during a
snowstorm, and jumped in front of a truck and died. Earlier that year, a
14-year-old boy, after taking one Tamiflu capsule, jumped or fell from the
ninth floor of an apartment building. Doctors say in both cases the boys had
not exhibited any abnormal behavior before taking Tamiflu.
Drug manufacturer Roche and US regulators have warned that influenza
patients treated with oseltamivir (Tamiflu) may have an increased risk of
self-injury and delirium. “People with the flu, particularly children, may
be at increased risk of self-injury and confusion shortly after taking
Tamiflu and should be closely monitored for signs of unusual behavior,” says
a warning that Roche has added to its official product information,
according to a company letter posted on the Food and Drug Administration
(FDA) Web site. …
Dr. Eleanor McBean, lived through the 1918 Influenza epidemic, and
testified, “As far as I could find out, the flu hit only the vaccinated.
Those who had refused the shots escaped the flu. My family had refused all
the vaccinations so we remained well all the time. There was seven times
more disease among the vaccinated soldiers than among the unvaccinated
civilians, and the diseases were those they had been vaccinated against.”
Vaccines, especially when given in multiple quantities in one sitting
certainly have the potential to throw a person or child’s body out of
balance as can nutritional deficiencies, dehydration, lack of exercise
or a lack of sun and vitamin D. Almost everyone today is magnesium
deficient, certainly every Mexican who eats white rice!
There are many who believe from the depths of their hearts that
vaccines are bio weapons of mass destruction, which exist for both
pharmaceutical profit and over bloated professional medical egos attached to
status and power. No matter what we believe though and no matter what
develops over the next few days it would be more than prudent to disseminate
this information that will be helpful to both doctors and people facing the
current public health crisis…
Retired biochemist and toxicologist Walter Last has this to say about
Lugol’s: “Lugol’s solution is an internal iodine
solution designed to eliminate Candida and possibly viruses and other
microbes from the bloodstream. Obtain 100ml of Lugol’s solution, also
labeled Aqueous Iodine Oral Solution B.P., from a chemist. Take a test drop
in liquid other then just water to make it taste less strong. If this does
not cause an allergic reaction, continue to take 4 x 6 drops daily in liquid
or mixed with food, but not together with vitamins A, C, E, grape seed
extract or cysteine. Iodine is an oxidant and it is best to reduce the
intake of antioxidants while using it. If the blood was contaminated, then
you may initially experience a die-off reaction of the Candida, causing
weakness and possibly headache or nausea. If this happens cut temporarily
back on the amount of Lugol’s solution and drink plenty of water and diluted
teas or juices. Continue for 3 weeks, but interrupt if you develop a serious
reaction. Do not take the iodine for more than 3 weeks as that interferes
with thyroid activity. If necessary repeat the course after several
months.”
[We are unable to determine the original source of the above compilation to give due credit; if anyone knows of its original publication, please let us know…. This in from Dr. Gayle on 05/01/09: “You are looking for Mark Sircus as the source on that post. Also KinChee was proven to kill avain flu virus in work in Japan and Korea.”]
————————————————–
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We reproduce below, with permission, A Solemn Walk Through “Food Safety”.
Index
Introduction
A Solemn Walk
Natural Solutions White Paper
———————————————-
Food is becoming a battle ground like no other: freedom, survival, fascistic take over of a once-free people (more or less, at least), corporate triumph over independent producers – it’s all happening around food. And the mechanism is simple: a set of bills ostensibly devoted to “food safety” and “food security”.
Urgent Action Item:
http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=26714
Tell Congress that the Farm Bills MUST be defeated. Time is short and the issue is of immense importance.
In essence, these bills are a sneak attack implementation of Codex Alimentarius. The Natural Solutions Foundation has been warning that organic farming and home growing, clean food and food freedom were under heavy attack. Here is the Mother of All Food Fascism Assaults and we still have some time to defeat it.
Congress often comes up with bad ideas. This is not just a bad idea: it is a catastrophically bad idea for health and freedom. In fact, it is nothing short of food tyranny and will kill not only organic farming, but lots of people as well, along with the entire private farming sector. Your own gardens are at risk as well.
I cannot urge you strongly enough to take action NOW (we have only a few days to create the urgent push-back needed to fend off this disastrous legislation. These are bad, deceptive and extraordinarily dangerous bills which make the eternal link between fascism and food crystal clear. But the bills are written in neutral, even calming tones. Please go to the articles below to read a brilliantly annotated version of the bills and a summary and learn just how dangerous they are. My thanks to Sue Diederich and Linn Cohen-Cole for their tireless work on this vital issue.
Just as –
~ “homeland security” is anything but assured by the Department of Homeland Security’s destruction of our rights,
~ “health” is not served by a healthcare system devoted to propagating illness for profit,
~ “democracy” is not served by corrupt voting machines and “man in the middle programs”
so food security and safety are not served by agencies and laws which –
~ drive independent farmers out of business,
~ forbid seed saving,
~ destroy safe food production and organic farming,
~ propagate dangerous and destructive industrial farming practices,
~ guarantee the total control of the food system by industrial forces known for unsafe food production while destroying the capacity of independent farmers to survive a regulatory onslaught created specifically to destroy them,
~ put home food production in jeopardy,
~ “HARMonize food production with pro-industry, pro-WTO controlled, lowest common denominator practices of Codex Alimentarius.
These are tragically solemn times calling for solemn re-dedication of each of us to the fight to retain and restore freedom. Food is just about the best place possible to start. Killing HR 875, S 425 and all related bills is the best place to start.
Click here (http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=26714) to tell Congress in no uncertain terms how imperative killing these dastardly bills is to you. Then tell everyone you know how important this push-back is.
Now think for a moment how important this information is to your life, your liberty and your society. Would you have had it without the Natural Solutions Foundation? We work very hard at being your health freedom advocates and we need your help. Please make regular donations, small or large, to the Natural Solutions Foundation – an astounding 100% of your donations goes directly to our work. People write to us to tell us that you need us and we certainly need you. Click here (http://drrimatruthreports.com/?page_id=189) to make your tax deductible donation to the Natural Solutions Foundation.
This action, and this issue, cannot wait.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.ValleyoftheMoonCoffee.org
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
Index ——————————————-
Solemn Walk Through HR 875
By Sue Diederich and Linn Cohen-Cole
Walk Index
First Walk: Myths and Misinformation
Second Walk: End of Organics
Third Walk: Meaning of the Bills
Fourth Walk: Conclusion
The Pennsylvania Sustainable Agriculture Association, PASA, sent out information about HR 875 which lists ‘facts’ to counter ‘myths’ and ‘rumors’ on the internet. It gives no specifics to back up its ‘facts,’ so the following close up view of the bill and accompanying commentary offers readers a chance to decide for themselves what is myth and what is fact. Neither of us are lawyers, but we both can read. Sue Diederich heads the Illinois Independent Consumers and Farmers Association, an organization formed to protect the rights of farmers and consumers to deal directly with each other without government interference.
PASA’s assertions are in regular lower case font, as are the inserted portions of the bill which have all been provided by Sue Diederich who also provides her own comments in italics usually. My comments are in bold face. [Note: these type faces have been altered from the original to permit publication in the program used to publish this blog which lacks color font options – Dr. Rima]
Occasionally, we feel something is essential for people to see and those comments are in CAPITAL LETTERS. (It should all be in CAPITAL LETTERS [font changed to allow publication in this program – Dr. Rima], really, since so few organizations appear to have read the bill or seem to know how to read the bill or have thought through its massive cumulative impact or been concerned at its endlessly broad reach and over incredibly vague things.)
People seem to expect the bill to be titled “The Criminalization of Organic Farming and the Take over of the US Food Supply,” and when they don’t see any words to that effect anywhere in the bill, they declare “this bill is fine” and those seeing dangers are “alarmists.” Do they think the industrial side is composed of fools? These are the same people who make cheery cereals with cartoon characters on the box when, inside, high fructose corn syrup is all over the cereal which comes from Bt-corn associated with diabetes. HFCS is, too, and there is an epidemic of diabetes here even among children. They know how to package. Why do people understand that industrial food inside a box can be a problem and yet are so innocent about looking at the bills, not realizing there is packaging there, too, or how much is at stake that the public and even legislators not see since this is about taking control. The industrial side isn’t stupid.
Understanding parts of the bill at times depends on smelling smoke as you read it. Here in the US, we still have only smoke … an Ohio state ag department SWAT team raid on an organic coop, Pennsylvania ag department raids on horse and buggy Mennonites, California setting coliform levels so low fresh milk dairy farmers would need cows that produced pasteurized milk right out the udder, arrest and handcuffing of a single mother in front of her children for selling goat milk, the USDA paying its agents bonuses for foreclosing on farms, … But in the EU where 60% of the Polish farmers are now gone because of identical bills enacted into law there, and 60 UK farmers have committed suicide, there is fire. And in Iraq, where they have been rendered helpless serfs by the theft of their country’s seeds and criminalization of farmers’ collection of their own seed, it is roaring. And in India where 182,000 farmers have committed suicide since the WTO and IMF got hold of agriculture and our Big Ag firms went in there, and 8 million farmers have left the land, it is out of control.
The WTO, run by the multinational meat packers and genetic engineering corporations, want HR 875, here. The bills are “harmonized” rules for globalization of food and lower food safety standards to allow for it. Those corporations are members of NIAA, a corporate consortium that brought NAIS, created by Anne Veneman, to the USDA to be made into law.
Walk Index
First Walk… Myths and Misinformation
We begin with PASA offering FWW’s take on the bills to its members:
Myths and Facts? H.R. 875 – The Food Safety Modernization Act
PASA members: The following information about a bill now before Congress, HR 875, was developed by our friends at Food and Water Watch, and forwarded to us by the National Sustainable Ag Coalition (NSAC), of which PASA is a member.
This Myth/Fact sheet was developed to help answer some of the rumors that are fairly rampant on the Internet right now. We will keep a close eye on the situation, and share further updates from NSAC as they become available. ?
MYTH: H.R. 875 “makes it illegal to grow your own garden” and would result in the “criminalization of the backyard gardner.”
FACT: There is no language in the bill that would regulate, penalize, or shut down backyard gardens. This bill is focused on ensuring the safety of foods sold in supermarkets.
Though private residences are not specifically included, nor are they specifically excluded. While this does not immediately affect home owners growing tomatoes in the backyard, entered testimony leaves the door open for just that in the future. Referring back to the Bio-Terrorism Act, in a discussion on this very topic and entered in the official record of debate on the interim rule, (bold/underline = mine), the same argument exists here and no new definitions or exclusions have been provided in HR 875 – and “reasonable” is a subjective term in theory as well as practice…
(13) FOOD ESTABLISHMENT-
(A) IN GENERAL- The term ‘food establishment’ means a
Slaughterhouse (except those regulated under the Federal Meat
Inspection Act or the Poultry Products Inspection Act), factory,
Warehouse, or facility owned or operated by a person located in
Any State that processes food or a facility that holds, stores,
Or transports food or food ingredients.
Now, every home in the country holds food after buying it from the
Grocery store. Will they be included too?
Hell, no. They’re going to be magnanimous and say that, while they could,
They won’t right now.
Excerpted from the same Interim Rule:
“(Response) FDA has concluded that private individual residences are
Not ”facilities” for purposes of the registration provision of the
Bioterrorism Act. Under the Bioterrorism Act, the term ”facility”
Includes ”any factory, warehouse, or establishment.” Congress did not Specify any definition for these terms.
Under their common meanings,
The terms can include private residences. For example, according to Webster’s II New Riverside University Dictionary (1994), the most
Relevant definition of ”establishment” is ”a business firm, club,
Institution, or residence, including its possessions and employees.”
However, ”[I]n determining whether Congress has specifically addressed
The question at issue, the court should not confine itself to examining
A particular statutory provision in isolation * * *.
It is a fundamental canon of statutory construction that the words of a
Statute must be read in their context and with a view to their place in
The overall statutory scheme.”’ FDA v. Brown & Williamson Tobacco
Corp., 529 U.S. 120, 121 (2000).
Other parts of the registration Provisions in section 415 of the FD&C Act indicate that Congress only Intended businesses to register, and raise a question as to whether Congress intended that private individual residences, even though food Is manufactured/processed, packed, or held at such residences, be Considered facilities.
For instance, a registrant is required to submit”the name and address of each facility at which, and all trade names Under which, the registrant conducts business * * * ” (21 U.S.C.
350d(a)(2)).
Thus it is unclear whether Congress intended all Individual private residences at which food is manufactured/processed, Packed, or held to be included in the term ”facility.” Furthermore, The requirement that a facility submit its ”name” as well as its ”trade names” raises a question as to whether Congress intended ”facility” to include private individual residences since it is Unlikely that a home would have a name or a trade name.
Where the words Of the statute are ambiguous, an agency may make a reasonable Interpretation of the statute. Chevron, USA, Inc. V. NRDC, Inc., 467 U.S. 837, 842-843 (1984); Brown & Williamson, supra, at 132.
Consistent with the language of section 415(a)(2) discussed
Previously, the agency concludes that interpreting the term
”facility” to exclude private individual residences is a reasonable
Construction for purposes of registration.
This interpretation, However, does not necessarily preclude a reasonable construction of Other provisions of the FD&C Act to include such residences.”
[I do get that residences are easily included.]
MYTH: H.R. 875 would mean a “goodbye to farmers markets” because the bill would “require such a burdensome complexity of rules, inspections, licensing, fees, and penalties for each farmer who wishes to sell locally – a fruit stand, at a farmers market.” ?
FACT: There is no language in the bill that would result in farmers markets being regulated, penalized any fines, or shut down. Farmers markets would be able to continue to flourish under the bill. In fact, the bill would insist that imported foods meet strict safety standards to ensure that unsafe imported foods are not competing with locally-grown foods.
SECTION 406 CLEARLY STATES ALL FOOD OFFERED FOR SALE WILL BE VIEWED AS BEING IN INTERSTATE COMMERCE AND SUBJECT TOT HE PROVISIONS OF THIS BILL.
C. 406. PRESUMPTION.
In any action to enforce the requirements of the food safety law, the connection with interstate commerce required for jurisdiction shall be presumed to exist
8) CATEGORY 4 FOOD ESTABLISHMENT- The term ‘category 4 food establishment’ means a food establishment that processes all other categories of food products not described in paragraphs (5) through (7).
(9) CATEGORY 5 FOOD ESTABLISHMENT- The term ‘category 5 food establishment’ means a food establishment that stores, holds, or transports food products prior to delivery for retail sale.
14) FOOD PRODUCTION FACILITY- The term ‘food production facility’ means any farm, ranch, orchard, vineyard, aquaculture facility, or confined animal-feeding operation.
[SUE, say it again and again, “this applies to farms and can apply to homes.” It certainly looks to me that families baking cookies for bake sales could easily be included.]
SEC. 206. FOOD PRODUCTION FACILITIES.
(a) Authorities- In carrying out the duties of the Administrator and the purposes of this Act, the Administrator shall have the authority, with respect to food production facilities, to–
(1) visit and inspect food production facilities in the United States and in foreign countries to determine if they are operating in compliance with the requirements of the food safety law;
(2) review food safety records as required to be kept by the Administrator under section 210 and for other food safety purposes;
(3) set good practice standards to protect the public and animal health and promote food safety;
(4) conduct monitoring and surveillance of animals, plants, products, or the environment, as appropriate; and
(5) collect and maintain information relevant to public health and farm practices.
(b) Inspection of Records- A food production facility shall permit the Administrator upon presentation of appropriate credentials and at reasonable times and in a reasonable manner, to have access to and ability to copy all records maintained by or on behalf of such food production establishment in any format (including paper or electronic) and at any location, that are necessary to assist the Administrator–
(1) to determine whether the food is contaminated, adulterated, or otherwise not in compliance with the food safety law; or
(2) to track the food in commerce.
(c) Regulations- Not later than 1 year after the date of the enactment of this Act, the Administrator, in consultation with the Secretary of Agriculture and representatives of State departments of agriculture, shall promulgate regulations to establish science-based minimum standards for the safe production of food by food production facilities. Such regulations shall–
(1) consider all relevant hazards, including those occurring naturally, and those that may be unintentionally or intentionally introduced;
(2) require each food production facility to have a written food safety plan that describes the likely hazards and preventive controls implemented to address those hazards;
(3) include, with respect to growing, harvesting, sorting, and storage operations, minimum standards related to fertilizer use, nutrients, hygiene, packaging, temperature controls, animal encroachment, and water;
THEY NEVER MENTION SEEDS BUT THIS IS PRECISELY HOW THEY WILL CRIMINALIZE SEED BANKING AND ALL HOLDINGS OF SEEDS.
[Notice they mention harvesting, sorting and storage operations, then watch below.
To follow how this will be done, you must understand that:
1. there is a small list inside the FDA called “sources of seed contamination”
2. in which they have now defined “seed” as food,
3. so seeds can be controlled under “food safety.”
Those seeds (so far) include:
seeds eaten raw such as flax, poppy sesame, etc.;
sprouting seeds such as wheat, beans, alfalfa, most greens, etc.;
seeds pressed into oils such as corn, sunflower, canola, etc.;
seeds used as animal feed such as soy ….
That is most seeds. Seeds are essential to life and thus to freedom.
The “sources of seed contamination” include six little items:
agricultural water
manure (but NOT chemical pesticides or fertilizers)
harvesting, transporting and seed cleaning equipment
seed storage facilities
What you must realize is that seed cleaning equipment is THE single most critical piece of equipment for sustainable agriculture. It is how we save organic seed. It is the machinery used after plants “go to seed” to separate out (sort) the seeds from the plant material so the farmer can collect (harvest) and then save (put in storage) seed for the next year at little cost. With his own seed, the farmer stays free of patented, genetically engineered, corporately privatized seeds.
You must also understand that Monsanto is getting rid of the people who do the seed cleaning and many other means of our having access to seed .
This year, 2009, seed cleaning equipment is now illegal in some parts of the country which tips us off to both the intent to control seeds in this way and to how they could do things under this bill.
How can they make such vital equipment illegal? Quietly, and by saying it contaminates food.
“Contaminate” is their favorite word since the public fears the deadly contamination that industry itself – not farmers – has caused. Scare the public and thus push for “food safety standards” to be set.
And to eliminate seed cleaning equipment, they haven now set the standards so seed cleaning (the simple separation of seed from plant) will now require a million to a million and a half dollar building and/or equipment … per line of seed.
So, a farmer who has been seed cleaning flax for 40 years with a hand made seed cleaner can’t sell flax on the market anymore, though there are NO instances of anyone ever having gotten sick from seed cleaning equipment. A farmer who has been cleaning wheat, corn and soy each year with the same perfectly fine equipment would now need three to four and half million dollars for three pieces of equipment to continue.
(The FDA isn’t so bar-setting when it comes to other things like melamine in baby formula, though it is proven to sicken and kill infants), initially denying the melamine was in our baby formula and then quickly inventing a “foods safety” standard to okay it.)
Organic farmers are not aware of this happening, perhaps because the left is being treated with kid gloves until HR 875 and related bills are/were passed. Meanwhile, the FDA and USDA have been tromping on traditional (many of them farming organically, by the way) farmers for years. The organic community is disconnected from them so hasn’t been aware of what is happening to them. Indie farmers have a history of no one listening to them, which is too bad because it is they who are the ones bringing the warning that these bills are deadly. The organic community, measuring against its own seeming safety, hasn’t heard or understood.
NOTICE, THOUGH, THAT BECAUSE A SINGLE “FOODS SAFETY” BAR HAS BEEN RAISED, IN TIME ON ONE WILL BE ABLE TO GET ORGANIC SEEDS IN ANY NUMBER BECAUSE IT WILL BE ILLEGAL FOR ALL FARMERS TO SELL THEM TO ANYONE.
Now, look at the last item on the list – seed storage facilities.
They would be careful not to ban them all outright given the extreme reaction they would get. But now the method is more clear. “Food safety” is the weapon and public fear is the driver and they only need to set the bar at the level that is impossible to meet.
Farmers, gardeners, seed saving exchanges, seed companies, scientific seed projects, and seed banks, all require “seed storage facilities.” All are working overtime to protect biodiversity that is rapidly disappearing because of … genetic engineering.
Set the standard for “food safety” and certification high enough that no one can afford it and punish anyone who tries to save seed in a multitude of ways that have worked fine for thousands of years, and PRESTO, YOU HAVE JUST CRIMINALIZED SEED BANKING.
The penalties, I will assume, will be tremendous, the better to protect us from nothing dangerous whatever, but to make monopoly over seed more absolute. One is left with control over farmers, and end to seed exchanges, to organic seed companies, to university programs developing nice normal hybrids.
When you know that Monsanto with the help of the US government plundered ancient and rare seed banks in Iraq that held seeds with a genetic heritage (a biohistory belonging to all of us) going back 1000s of years and then made it a crime for farmers there to collect or use their own normal and non-patented seeds off their own land, you see how extreme the intent to control is.
Now, perhaps it is possible to see how the identical thing is being done here, only it comes in a heavily, heavily disguised way – through “food safety” that isn’t at all – and in only one tiny little paragraph within a very large bill.
The Iraqis are now abjectly dependent on Monsanto and the US for survival itself and will have to pay whatever prices are set for food. They cannot just grow their own and be free. So, no matter what form of government they may have, they are now slaves because the control over them is that extreme. Kissinger was right – control food and you control people.
This trick of setting bars above any ability to be in the game, is similar to how blacks had been treated. Click here. This trick of setting bars above any ability to be in the game while imposing fines that destroy people who fail to meet that standard, is sadistic. Then, taking the land as confiscatory payment, is theft by government become totalitarian and colonizing its own people.
There are other items of the list which surely will be controlled as well. In toto, that little list is the deconstruction of farming itself and given the inclusion of manure, especially of organic farming.]
(4) include, with respect to animals raised for food, minimum standards related to the animal’s health, feed, and environment which bear on the safety of food for human consumption;
(5) provide a reasonable period of time for compliance, taking into account the needs of small businesses for additional time to comply;
(6) provide for coordination of education and enforcement activities by State and local officials, as designated by the Governors of the respective States; and
(7) include a description of the variance process under subsection (d) and the types of permissible variances which the Administrator may grant under such process.
(d) Variances- States and foreign countries that export produce intended for consumption in the United States may request from the Administrator variances from the requirements of the regulations under subsection (c). A request shall–
(1) be in writing;
(2) describe the reasons the variance is necessary;
(3) describe the procedures, processes, and practices that will be followed under the variance to ensure produce is not adulterated; and
(4) contain any other information required by the Administrator.
(e) Approval or Disapproval of Variances- If the Administrator determines after review of a request under subsection (d) that the requested variance provides equivalent protections to those promulgated under subsection (c), the Administrator may approve the request. The Administrator shall deny a request if it is–
(1) not sufficiently detailed to permit a determination;
(2) fails to cite sufficient grounds for allowing a variance; or
(3) does not provide reasonable assurances that the produce will not be adulterated.
(f) Enforcement- The Administrator may coordinate with the agency or department designated by the Governor of each State to perform activities to ensure compliance with this section.
(g) Imported Produce- Not later than 1 year after the date of the enactment of this Act, the Administrator shall promulgate regulations to ensure that raw agricultural commodities and minimally processed produce imported into the United States can meet standards for food safety, inspection, labeling, and consumer protection that are at least equal to standards applicable to such commodities and produce produced in the United States.
Administrator shall have authority to grant exclusions to foreign producers.
[While it may be obvious to us that this is onerous beyond any capability of coping with it, it needs to be said and described in some detail what it would actually mean for farmers or for us. Here in story form is a taste of it, so anyone could feel the insanity of it:
SEC. 201. ADMINISTRATION OF NATIONAL PROGRAM.
(a) In General- The Administrator shall–
(1) develop, administer, and annually update a national food safety program (referred to in this section as the ‘program’) to protect public health; and
(2) ensure that persons who produce, process, or distribute food meet their responsibility to prevent or minimize food safety hazards related to their products.
[This is where I think it would be very helpful if you explained how astoundingly onerous that long list is and what its impact would be on any farmer who previously only needed to load up his goods and bringing them to a farmers market – though that in itself is a time consuming, physically effortful job that often begins pre-dawn on those mornings and ends late in the day, all of it separate from growing the food and boxing it up to bring.
A small farm is not an industry with staff to fill out paperwork, handle licensing, manage all the industrial bureaucracy that is being loaded on here, but is most often a couple who is also taking care of a family in addition to growing crops and raising animals. These are precisely the people who we need most as part of our food system and how will clearly be crushed by the grossly inappropriate application of such rules to small farms.]
· MYTH: H.R. 875 would result in the “death of organic farming.”
FACT: There is no language in the bill that would stop organic farming. The National Organic Program (NOP) is under the jurisdiction of the United States Department of Agriculture (USDA). The Food Safety Modernization Act only addresses food safety issues under the jurisdiction of the Food and Drug Administration (FDA).
[Of course, they are not going to come straight out and say it. But breaking this down to what is actually involved, you find that:]
The administrator is charged with developing minimum standards, not maximum limits on feed, fertilizers, nutrients etc- right here goes organics.
Secondly, this act creates a new agency, and the FDA becomes the Federal Drug and Device Agency. It combines offices currently under FDA and Commerce Department (National Marine Fisheries).
Third, FSA is to cooperate with the USDA in “promulgating rules and orders” which will have the bearing and impact of law.
To refer back to the previous “Myth”
[The one about foreign food having to meet our standard, right?]
– Alaska, Hawaii, US territories and foreign countries may apply for variances, so… NO… Imported foods do NOT necessarily have to meet the same standards. In fact, many countries have had to lower their standards due to WTO rules and trade agreements, and Australia had to further lower their regulatory standards when they instituted the NLIS program (their version of NAIS). There is no reason to think we would not have to do the same.
Walk Index
Second Walk… The End of Organic Farming
[NOW, COMES THE RESPONSE TO WHETHER THE BILLS WILL MEAN THE END OF ORGANIC FARMING.]
I’m going to format this differently to accentuate your points, Sue. This section should be a major education for people in how things have been working. This is in response to the myth that the bills will not affect organic farming, right?]
Animal health has traditionally meant medication and hormones, petroleum-based fly sprays and all sorts of other goodies.
Feed can be anything (GMO SOY OR CORN, ANYONE?),
environment can mean PESTICIDES, HERBICIDES USED ON PASTURES (IF pasturing is deemed “healthy” – internationally this is NOT so for poultry, in fact in many countries there is NO outdoor poultry anymore – by law).
Nutrients are not necessarily whole food based, many are produced SYNTHETICally, and again, PETROLEUM BASED …
Animal encroachment prevention can be anything from a scarecrow or plastic owl to POISON BATES AND BULLETS. Not one of these things is specified, yet there is no place for real public opinion in the decision making process provided. I will grant that there is usually a public comment period for federal register entries, for whatever that has been worth in the past.
[Meaning, it has been worth little to nothing. And obviously, the public is left having to respond ad infinitum to one issue after another. Someone compared the numbers of things being thrown at us to try to stop, to carpet bombing so you can’t comment on everything, even if it helped which is clearly often doesn’t.]
SEC. 206. FOOD PRODUCTION FACILITIES.
(a) AUTHORITIES.—In carrying out the duties of the Administrator and the purposes of this Act, the Administrator shall have the authority, with respect to food production facilities, to
(1) visit and inspect food production facilities in the United States and in foreign countries to determine if they are operating in compliance with the requirements of the food safety law;
(2) review food safety records as required to be kept by the Administrator under section 210 and for other food safety purposes;
(3) SET GOOD PRACTICE STANDARDS to protect the public and animal health and promote food safety;
[This is where words that sound so friendly and innocuous and even good are code words for international rules set by the WTO that actually define industrial requirements which do not fit real farming in the least, much less organic farming, would be applied.
[This is where insane, anti-nature, anti-farming rules like “animals and crops can’t exist on the same farm” come into play. Where wild animals aren’t ever supposed to be near crops so the government has been poisoning deer and frogs. The list of such manufacturing rules for farming is long, and each very much “efficiency manager comes and wrecks the farm.”]
(4) conduct monitoring and surveillance of animals, plants, products, or the environment, as appropriate; and
[Please, those of you who find the idea of NSA-spying intolerable, look carefully at those words. Now, imagine it were your farm, your home on that farm, and realize that the USDA and FDA have been run by and the new agency will be run by Monsanto, Cargill, Tysons, ADM. Their interest in helping consumers have safer food is nil The bills are meant to eliminate farmers as is now rapidly occurring in the EU with identical (“harmonized”) bills, now law there.
(5) collect and maintain information relevant to public health and farm practices.
[There needs to be a pause here to consider the implications of each of those on someone’s home – their family’s farm. This is quite different from applying them to industrial sites where no one lives, and beyond that, these powers are so broad and vague, they are dangerous if only in that.
Those things listed open the door to total control, warrantless entry and perpetual surveillance. Notice how innocuous they have made it appear, even beneficial – always about public health. Yet, the insincerity of this is boggling – the USDA and Big Ag have worked to prevent inspections to the point where farmers have had to actully sue to get them done , even after offering to pay for them.]
(b) INSPECTION OF RECORDS.—A food production facility shall permit the Administrator upon presentation of appropriate credentials and at reasonable times and in a reasonable manner
[Who defines “reasonable”? Does a farmer have to go to court each time there is an “unreasonable” manner and time? How wide open do we push the door to Big Ag-corrupted government control over farmers – the people creating the only safe food?
Look carefully and realize the USDA right now is countenancing state ag departments conducting terrorizing raids on non-corporate farms across the country. Imagine it were your home and USDA agents banging on your door to demand paper work and if you don’t have it, facing fines that would bankrupt you in a moment and lose you your land and home.]
, to have access to and ability to copy all records maintained by or on behalf of such food production establishment in any format (including paper or electronic) and at any location, that are necessary to assist the Administrator—
[Imagine again.]
(1) to determine whether the food is contaminated, adulterated, or otherwise not in compliance with the food safety law; or
[Be aware that in Pennsylvania where there has been an aggressive effort to destroy fresh milk dairy farmers, the tests by the states repeatedly do not match those of independent testers but the harm to farmers from such false tests and reporting of them is done and can’t be undone. Be aware that the USDA has a record of creating test results damaging to small farmers while it refuses to inspect even when farmers ask to pay.]
(2) to track the food in commerce.
[This could mean farmers bringing food to markets with USDA agents surveilling.]
(c) REGULATIONS.—Not later than 1 year after the date of the enactment of this Act, the Administrator, in consultation with the Secretary of Agriculture and representatives of State departments of agriculture, shall promulgate regulations to establish science-based minimum standards for the safe production of food by food production facilities. Such regulations shall—
[Everything in this bill is being left to be filled in however the “Food Safety Tsar” – “the Administrator” decides? Right now, to give people pause and to wake them up a bit to how this is not a wise idea but in fact absurd, it appears that person could be Michael Taylor, a Monsanto lawyer infamous for approving rBGH – the first genetically engineered product ever approved – over the objections of doctors, scientists who said the numbers were being rigged, and the public.
How can anyone leave a bill so utterly vague in the hands of anyone to decide later what it all means? Do we not make laws here with specific meaning anymore? Or do we simply let totalitarian rules be applied by industry against non-industrial entities like farms and homes in any way they wish and with immense police power behind what they, for their own interests, decide?]
(1) consider all relevant hazards, including those occurring naturally, and those that may be unintentionally or intentionally introduced;
[GOODBY RAW MILK.]
(2) require each food production facility to have a written food safety plan that describes the likely hazards and preventive controls implemented to address those hazards;
(3) include, with respect to growing, harvesting, sorting, and storage operations, minimum standards related to fertilizer use, NUTRIENTS, HYGIENE, PACKAGING, TEMPERATURE CONTROLS, ANIMAL ENCROACHMENT, AND WATER;
[GOODBYE ORGANIC FARMING.]
(4) include, with respect to animals raised for food, MINIMUM STANDARDS related to the animal’s HEALTH, FEED AND ENVIRONMENT which bear on the safety of food for human consumption;
[GOODBYE ORGANIC FARMING AND GRASS FED ANIMALS.]
(5) provide a reasonable period of time for compliance, taking into account the needs of small businesses for additional time to comply;
[Oh, heavens, this looks like padding to throw in the word “reasonable” again but it has no explicit meaning whatever and so no safety for a soul.]
(6) provide for coordination of education and enforcement activities by State and local officials, as designated by the Governors of the respective States; and
[This appears to be where Homeland Security works with the USDA for such things as “depopulation of animals” – for which 6 meetings are already scheduled in June and into which livestock owners are not allowed though foreigners are.
These “depopulation” plans look like what is happening in Asia where animal disease caused by industry (and worth a fortune to the pharmaceutical industry ) are then used by industry to wipe out its competition in heritage breeds of animals on small farms and to substitute genetically engineered animals that are patented by industry and thus owned by industry.
(7) include a description of the variance process under subsection (d) and the types of permissible variances which the Administrator may grant under such process.
(d) VARIANCES.—
.
[This is where the “fact” that foreign countries must meet our food safety requirements collapses by simply reading the bill.]
MYTH: The bill would implement a national animal ID system.?
FACT: There is no language in the bill that would implement a national animal ID system. Animal identification issues are under the jurisdiction of the USDA. The Food Safety Modernization Act addresses issues under the jurisdiction of the FDA.
This bill mandates NAIS BY claiming that it is already law,
then contradicts itself by citing COOL, which specifically prohibits mandatory tracking.
It justifies NAIS by claiming that the AHPA gives authority – but this is a bill (and supposedly a program) concerning interstate commerce (though any item of food for sale is “presumed” to be in interstate commerce, whether it is in reality or not.) and AHPA does not regulate interstate commerce.
How many contradictions in a single section do we need before red flags go up?
[YES, AND PUT UP RED FLAGS FOR WHOLE BILLS IF THIS CENTRAL PART IS SO CORRUPTLY BEING PUSHED.]
Below in CAPITALS [fonts altered – Dr. Rima] , Sue answers the absurd claim that NAIS is not mandatory. FWW has gotten this and many other items wrong. That would be fine if the whole organic movement and all our farms and freedom were not riding on our seeing these very real threats and stopping those bills completely – not compromising on them but demanding their complete withdrawal.]
(a) IN GENERAL – THE ADMINISTRATOR, IN ORDER TO PROTECT THE PUBLIC HEALTH, SHALL ESTABLISH A NATIONAL TRACEABILITY SYSTEM THAT ENABLES THE ADMINISTRATOR TO RETRIEVE THE HISTORY, USE AND LOCATION OF AN ARTICLE OF FOOD THROUGH ALL STAGES OF ITSPRODUCTION, PROCESSIN, AND DISTRIBUTION.
(b) APPLICABILITY – TRACEABILITY REQUIREMENTS UNDER THIS SECTION SHALL APPLY TO FOOD FROM FOOD PRODUCTION FACILITIES, FOOD ESTABLISHMENTS, AND FOREIGN FOOD ESTABLISHMENTS.
(c) REQUIREMENTS-
(1) STANDARDS- THE ADMINISTRATOR SHALL ESTABLISH STANDARDS FOR THE TYPE OF INFORMATION, FORMAT, AND TIMEFRAME FOR FOOD PRODUCTION FACILTITIES AND FOOD ESTABLISHMENTS TO SUBMIT RECORDS TO AID THE ADMINISTRATOR IN EFFECTIVELY RETRIEVING THE HISTORY, USE AND LOCATION OF AN ITEM OF FOOD.
(2) RULE OF CONSTRUCTION- Nothing in this section shall be construed as requiring the Administrator to prescribe a specific technology for the maintenance of records or labeling of food to carry out the requirements of this section.
(3) AVAILABILITY OF RECORDS FOR INSPECTION- Any records that are required by the Administrator under this section shall be available for inspection by the Administrator upon oral or written request.
(4) DEMONSTRATION OF ABILITY- The Administrator, during any inspection, may require a food establishment to demonstrate its ability to trace an item of food and submit the information in the format and time frame required under paragraph (1).
(d) Relationship to Other Requirements-
(1) CONSISTENCY WITH EXISTING STATUTES AND REGULATIONS- To the extent possible, the Administrator should establish the national traceability system under this section to be consistent with existing statutes and regulations that require recordkeeping or labeling for identifying the origin or history of food or food animals.
[Does this mean consistent with international laws under the WTO? Is this a means of locking everything together into Smart Grid or NAFTA or CAFTA or GATT and even, the worst of all,
?]
(2) EXISTING LAWS- For purposes of this subsection, the Administrator should review the following:
(A) Country of origin labeling requirements of subtitle D of the Agricultural Marketing Act of 1946 (7 U.S.C. 1638 et seq.).
(B) The Perishable Agricultural Commodities Act of 1930 (7 U.S.C. 499a-t).
(C) Country of origin labeling requirements of section 304 of the Tariff Act of 1930 (19 U.S.C. 1340).
(D) The National Animal Identification System as authorized by the Animal Health Protection Act of 2002 (7 U.S.C. 8301 et seq.).
EC. 210. TRACEBACK REQUIREMENTS.
MYTH: The bill is supported by the large agribusiness industry.?
FACT: No large agribusiness companies have expressed support for this bill.
This bill is being supported by several Members of Congress who have strong progressive records on issues involving farmers markets, organic farming, and locally-grown foods.
[Who almost certainly have not read the bills or can’t interpret how it will work to destroy farmers, organic food, seed banking, and all of us.]
Also, H.R. 875 is the only food safety legislation that has been supported by all the major consumer and food safety groups, including:
[Perhaps others know details on each organization and why they might be supporting a bill that is so threatening to real food safety and to the survival of our farms and organic farming.]
?– Center for Foodborne Illness Research & Prevention
?– Center for Science in the Public Interest
?– Consumer Federation of America
The Consumer Federation of America (CFA) is a long-standing consumer organization based in Washington, DC. However, it has accepted funding from the ROCKEFELLER FOUNDATION to “develop an optimum regulatory regime” for genetically engineered food.
?– Consumers Union?– Food & Water Watch
[Food and Water Watch just put out a description of the bill in which it is apparent they do not understand what is in it and what it will do. With that as their starting point, they support it.]
?– The Pew Charitable Trusts
[They are also connected to the ROCKEFELLER FOUNDATION, and involved with them in mandatory vaccinations programs around the world and issues of reducing population.]
?– Safe Tables Our Priority ?– Trust for America’s Health
[There is no list here of groups opposing this bill, which include the people whose lives are most at risk from it and who know its dangers the best and who should have been the first people consulted. Instead, they have been shut out and when they have tried to report extreme dangers, they have ignored, dismissed, marginalized. Perhaps the other organizations listed here are as unfamiliar with the bill’s contents and ramifications as FWW.]
If you consider that not only is Rosa DeLauro married to Stanley Greenberg, who boasts Monsanto as one of his clients, but also that she receives the largest donations from agribusiness PAC’s of just about anyone in Congress, does industry NEED to come out and say they support this particular bill? If cash to the sponsor doesn’t count, and if formal positions supporting various specific aspects of the bill do not count, then what does? Would there not be massive public backlash against it if industry DID take a formal stand on every bill they want to see passed?
By the same token, I’ve not seen a single industrial ag company come out and oppose this bill, either. They have all been conspicuously silent. I seem to remember that they threw up quite a fuss over COOL, and caused enforcement to fall behind by more than 7 years… Not to mention the garbage with loopholes we’ve had to deal with since enforcement began. (What good does a “Canada, US, Mexico” label do for anybody? Especially with BSE in Canada and TB coming in daily from Mexico?) Where’s the hoot and holler over this?
MYTH: The bill will pass the Congress next week without amendments or debate.?
FACT: Food safety legislation has yet to be considered by any Congressional committee.?
I can’t speak to the time frame. [Note from NSF: our sources “on the Hill” told us they believed these bills had been “fast tracked” to be passed during President Obama’s “First 100 Days”]
[It came from those who first discovered the bills were there, inserted only one week after Vilsack had said the USDA wasn’t even considering centralizing the FDA and USDA at this time, so people saw how similar the bills were, knew who fast other things were being shoved through Congress without even reading those bills, and estimated how fast this could happen.
Perhaps with people alerted now, these bogus “food safety” bills can be stopped by the organic community once it realizes they will utterly destroy it.]
However, since I did have the luxury of listening to the farce taking place on the floor of the House of Representatives on March 11 concerning HR1105 (which FUNDS NAIS among its hundreds of other projects) while awaiting the Livestock, Dairy and Poultry subcommittee hearing on NAIS – I have no doubt that this bill will move quickly now that 1105 has passed and since it has so many co-sponsors.
Especially since the Representatives were honest enough to admit that though the Senators claimed everybill in the Omnibus Act had been heard and passed in the previous session, when in actuality, some 100 of the 170 bills in the package had NOT.
But this is my personal opinion.
The “ominous Omnibus Act” as several Representatives called it, went from introduction to the President in less than 13 working days.
I really have to question just who’s side those groups are really on that are in support of this bill…..
And finally,
Walk Index
Third Walk… Meaning of the Bills
WHAT THE NEW “FOOD SAFETY” BILLS MEAN TO YOU
by Gail Combs
Our food safety system was trashed in 1995 by Sec of Ag Ann Veneman (Board member of Monsanto). She appointed Dan Amstutz (VP of Cargill) who wrote the World Trade Organization Agreement on Agriculture (WTO AoA). Unlike GATT, WTO has major clout from trade sanctions and control of 90% of the international trade. http://www.publiceyeonscience.ch/images/the_wto_and_the_politics_of_gmo.doc
“Aims to ensure that governments do not use quarantine and food safety requirements as Unjustified trade barriers.. It provides Member countries with a right to implement traceability {NAIS} as an SPS measure.” WTO
In other words the WTO did away with “quarantine and food safety requirements” that gave us “the safest food in the world” and is graciously going to allow Farmers to track AND COUNT the world’s livestock for them instead. Now HR 875 and an FDA release indicate All food will be tracked and all food producers will have Food inspections and the threat of fines up to $1,000,000 a day will eliminate all the independent farms that have acted as a check on Corporate AG.
The FDA wants
to implement a more effective trace-back process, using technologies to rapidly and precisely track the origin and destination of contaminated foods, feed and ingredients
Nanotech in Food can make it happen “California’s Oxonica makes Nanobarcodes from nano-particles that contain silver and gold stripes varying in width, length and amount, such that billions of combinations can be created to tag individual products. The barcodes have been primarily used to assure brand and authenticity in pharmaceuticals, but applications could be forthcoming in tracing food batches”.
In regard to pets:
HR 875 uses “animals” and then “animals raised for food” and there are no exclusions. The Animal Welfare Act had exclusions for livestock, pets and people raising three or less litters of puppies a year. Therefore pets are not excluded.
“set good practice standards to protect the public and animal health and promote food safety”
“conduct monitoring and surveillance of animals, plants, products, or the environment, as appropriate”
“with respect to animals raised for food, minimum standards related to the animal’s health, feed, and environment which bear on the safety of food for human consumption;
In regard to gardens:
The Feds Already have plans for controlling food “FROM FARM TO FORK” including home preparation since September of 1995 (WTO ratified in 1995)
HR 875
“require each food production facility to have a written food safety plan that describes the likely hazards and preventive controls implemented to address those hazards;”
“include, with respect to growing, harvesting, sorting, and storage operations, minimum standards related to fertilizer use, nutrients, hygiene, packaging, temperature controls, animal encroachment, and water”
“include, with respect to animals raised for food, minimum standards related to the animal’s health, feed, and environment which bear on the safety of food for human consumption;”
“set good practice standards to protect the public and animal health and promote food safety”
“..facility owned or operated by a person located in any State that processes food or a facility that holds, stores, or transports food or food ingredients.”
Notice it does not say a person SELLING food, it says a person holds, stores, or transports food or food ingredients. The bill specifically states it covers commerce with in state but again there is no exclusion for food raised for home use. The fact you are growing veggies for your and friends and not selling them does not exclude you.
“in any action to enforce the requirements of the food safety law, the connection with interstate commerce required for jurisdiction SHALL BE PRESUMED TO EXIST.”
Under Ag Sec. Veneman …
in September, 1995, the USDA’s Food Safety & Inspection Service presented a 600-page document “Farm-To-Table” intended to control of every step in the food chain from production to home preparation.
This is a real life example of what has already occurred and what people may have in store:
Today a state Ag inspector and two county officials show up and scare the bee-jesus out of me. First they accuse me of selling products and milk, then explain that even “giving milk products away” is illegal in California. Now everything is pasteurized, but it is illegal to share milk products in any form! They explained it was even ILLEGAL to give it to my own children if they did not live under my roof! I can’t even take a lasagna dish to my grown sons home without risk of being fined, arrested and or jailed! This is OUTRAGEOUS!!!!…..” Donna Tue Aug 12, 2008 http://finance.groups.yahoo.com/group/Americans_Against_NAIS/message/26452
More stories on Feds raiding farms and co-ops
Walk Index
Last Walk… Conclusion
The related package of “food safety” bills are totalitarian. There are no two ways about it.
They allow government warrantless intrusion into and extreme, detailed, surveilled control over every aspect of farmers’ land and home, straight-jacketing them into a bureaucratic nightmare which precludes their even functioning as farmers. And yet for real food safety and for food security, it is exactly farmers we need.
We need the real food they produce and the farmland they spare and protect from industrialization and the heritage animals and seeds they raise and their knowledge about nature and animals, and we need the way of life they represent. Free. How interesting that to have real and clean and wholesome food, it requires that farmers have freedom.
These bills which claim to be about “food safety” but are proven in the EU already to be about the destruction of farmers, are so frighteningly broad, they allow the government to take over our lives, too. They allow the government to use rules written by multinational corporations within the WTO, to control whether we can garden or how, whether we chip our pets, even what happens inside our homes in our kitchens.
These controls all all for mandating things that make money for corporations just as we are all trying to get off the corporate grid of power, fuel, food, … Now it is easy to appreciate people’ resistance to mandated vaccines (and they keep adding more kinds).
There is point at which we must say stop. Our lives are our own, our property is our own, our decisions on what to eat and how to heal ourselves are our own. We must protect our own freedom and now it is apparent how intimately tied it is those who have been providing for us for ever – our farmers.
HR 875, SR 425, HR 814, HR 759 and all related bills must be withdrawn immediately and then trashed.
http://www.opednews.com/articles/A-solemn-walk-through-HR-8-by-Linn-Cohen-Cole-090314-67.html
Index ———————————-
Further information linking Codex Alimentarius (the World Food Code) and the (sic) Food (sic) Safety bills, see:
A Natural Solutions Foundation White Paper
Regarding U.S. Codex Office and Food Safety and Inspection Service (FSIS) for
Adoption of Codex Committee Policies by the U.S. Codex Delegation and FSIS
in Harmony with the Dietary Substances Health and Education Act (DSHEA),
19 USC 3512 (the Anti-Harmonization Statute) and other Statutory and Case Law
The careless, industry controlled FDA has been happy to approve drugs made from genetically modified molecules, including many from plants, since 1985 when it approved GMO insulin. These drugs are called “Biologicals”. A new analysis, published in the Journal of the American Medical Association, shows that biologicals are twice as dangerous as chemical (non GMO) drugs. We know how dangerous they are (over 100,000 deaths per year and 3 million hospitalizations per year for adverse events from properly used drugs in the US each year. Now multiply that danger by at least two and see what you get: a profit-driven disaster.
The excellent summary below makes it clear that while it is essential to divest the FDA and USDA of their food regulatory responsibilities, the dangerous and industry-supported FDA is not doing any better with their regulatory responsibilities on drugs than they are on food. At least with drugs, however, you have a chance, for the moment, of saying “yes” or “no” to their use. Food is compulsory. Drugs are [usually] voluntary. And that is why, of course, natural medicine options, in all their forms, are under such vigorous attack.
That is also why the Natural Solutions Foundation continually asks you to make sure that everyone in your contact list becomes aware of these issues and that you request that they take the actions that you take to prevent the loss of our health freedoms and to separate this dangerous agency (and the USDA) from your table and your health.
Here is the link to send to your contact list so they can sign up for the free, secure and vitally important Health Freedom Action eAlerts: http://drrimatruthreports.com/?page_id=187. And here is the link for you – and your contacts – to make a tax exempt donation to the Natural Solutions Foundation: http://drrimatruthreports.com/?page_id=189.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
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‘Biologicals’, Wonder Drugs with Problems
Protein drugs produced by genetic engineering cause adverse events including death more frequently than synthetic chemical drugs; yet they are being produced in transgenic crops grown in open fields Prof. Joe Cummins
‘Biologicals’ more dangerous than chemicals
‘Biologicals’ are drugs in which the active substance is produced by or extracted from a biological source (in contrast to synthetic chemicals). Biologicals are relatively recent, being for the most part, recombinant proteins produced by genetic engineering. The first biological was recombinant human insulin produced in recombinant bacteria and commercially approved in 1982. Currently, there are more than 250 biologicals on the market, including recombinant blood products, monoclonal antibodies and vaccines that have been approved by regulatory agencies in the United States and European Union (EU). Between 2003 and 2006 biologicals represented 24 percent of all new approvals in the US and 22 percent of new approvals in the EU [1]. Ten biologicals are listed among the top selling ‘blockbuster’ drugs valued at 1 to 3.2 billion dollars in sales. These drugs included treatments for red blood cell disorders, immune system disorders, cancer and insulin analogues [2].
Newly approved drugs are frequently found to cause unexpected problems; but biologicals are incurring problems even more frequently than synthetic chemical drugs. A recent study published in the Journal of the American Medical Association confirms that the biological drugs have provoked significantly more regulatory actions than newly introduced synthetic chemical drugs. The researchers, based in The Netherlands, followed up a group of biologicals approved in the US and EU between 1995 and 2008, and found that 24 percent of these have prompted safety regulatory actions. New chemical drugs have an 8.5 percent chance of safety warning within ten years of approval, compared to 17 percent for biologics [2]. The regulatory actions included warnings on general disorders and administration site conditions, infections and infestations, immune system disorders and cancers (benign, malignant and unspecified). Adverse events included many serious complications of the drug treatment such as increased mortality, anaphylaxis, cancer, heart failure, stroke, and infections [1]. However, industry representatives implied [2] that the diseases being treated were very serious, and the drugs were efficacious and the adverse events relatively rare. The study concluded [1]: “The nature of safety problems identified after approval for biologicals is often related to the immunomodulatory effect (infections). Because the biologicals first to be approved in a class were more likely to be subjected to regulatory action, close monitoring is recommended.”
FDA blaming the victims rather than the drugs?
A review of the Netherlands study published in Nature Biotechnology acknowledges the significance of the study and the problem of adverse events related to biologicals. The article mentions a caveat to the study’s conclusions added by Sandra Kweder, deputy director of FDA’s office of new drugs at the Center for Drug Evaluation and Research [2]: “Biological therapeutics are more likely to be developed to treat serious illnesses, she points out, and serious illnesses themselves are fertile ground for ‘toxicity’ whether related to the drug or disease, so interpreting data on the drug’s or biological’s risk must take that into account.” That seems to lay the blame for the adverse outcomes on those being treated rather than the drugs; and looks like an attempt to protect the billion-dollar industry.
The Nature Biotechnology review [2] further comments that industry insiders agree long-term safety monitoring will be crucial for biologics. While the antibody producing company InNexux’s chief scientific officer is reported to have said: “That long-term use may lead to problems I think is a given,” – a suspicion borne out by the latest study – the company’s chairman and ceo Jeff Morhet, finds at least one important consolation: “the study showed that no biological was pulled from the market for safety reasons.”
Lax FDA regulation and a profit-hungry industry
If anything, Morhet’s remark should offer no consolation to those being treated; as it exposes the lack of adequate regulation to protect the public in face of ‘miracle cures’ being offered by an industry whose primary concern is profit.
Significantly, no one has commented on the 2005 case of the drug Tysabri (natalizumab) a treatment for multiple sclerosis that was suspended following two deaths of patients from leukoencephalopathy (progressive damage or inflammation of the white matter of the brain) [3]. Nor indeed has anyone mentioned the catastrophic London drug trial of a biological monoclonal antibody drug that left six healthy young volunteers seriously ill [4] (London Drug Trial Catastrophe – Collapse of Science and Ethics, SiS 30).
The Institute of Science in Society (ISIS) has long been critical of the manner in which biological are tested and used in treatment. The adverse event, ‘cytokine storm’ unleashed in the immune system of the volunteers, was not exactly a surprise. The FDA had issued a long list of warnings on similar monoclonal antibody drugs [5] (Warnings on FDA Approved Monoclonal Antibody Drugs, SiS 30); but that seemed to have been ignored [6] (Post Mortem on the TGN1412 Disaster, SiS 30).
Pharm crops with dangerous biologicals in open field trials put the public at risk
Even more seriously, the secret trials of food crops (pharm crops) in open fields modified with mammalian genes expressing proteins used to treat human or animal disease continue unabated [7] (Drug Trial Catastrophe & Safety of Secretly Tested Pharm Crops, SiS 30). Pharm crops for vaccines and therapeutic antibodies have been trialed since 2004 and earlier [8] (Pharm Crops for Vaccines and Therapeutic Antibodies, SiS 24). Antibodies are produced in tobacco plants [9] (Antibodies from Hybrid GM Tobacco Plants, SiS 35) and in maize [10] (Transgenic Maize with Monoclonal Antibodies Grown in France, SiS 35). Biologicals are well known to have severe side effects on patients and on healthy people. There is no justification for exposing the unsuspecting public to these drugs produced in pharm crops grown in open fields.
References
1. Giezen TJ, Mantel-Teeuwisse AK, Straus SM, Schellekens H, Leufkens HG, Egberts AC. Safety-related regulatory actions for biologicals approved in the United States and the European Union. JAMA. 2008, 300(16), 1887-96.
2. King J. JAMA casts cloud over biologic safety. Nature Biotechnology 2009, 27,11-12.
3. FDA Public Health Advisory Suspendec Marketing of Tysabri (natalizumab) 2005 updated 2007 http://www.fda.gov/cder/drug/advisory/natalizumab.htm
4. Ho M-W and Cummins J. London drug scandal catastrophe, collapse of science and ethics Science in Society 30, 41-43. 2006.
5. Cummins J. Warning on FDA approved monoclonal antibody drugs Science in Science in Society 30, 46-47. 2006.
6. Saunders PT. Post mortem on the TGN1412 disaster. Science in Society 30, 44-45+47,. 2006.
7. Cummins J and Ho M-W. Drug trial catastrophe & safety of secretlytested pharm crops Science in Society 30, 50, 2006.
8. Cummins J. Pharm crops for vaccines and therapeutic antibodies Science in Society 24, 22-23, 2004.
9. Cummins J and Ho M-W. Antibodies from hybrid GM tobacco plants. Science in Society 35, 51, 2007.
10. Cummins J, Ho M-W and Saunders PT. Transgenic maize with monoclonal antibodies grown in France Science in Society 31, 4, 2006.
ttp://www.i-sis.org.uk/biologicalsWonderDrugsWithProblems.php
Barbara Loe Fisher is a tireless advocate of both vaccine truth and choice and the Natural Solutions Foundation nominates her for our Hall of Fame. Barbara continues to examine carefully the vaccine industry, its products and its corruption. Her site, www.NVIC.org, is a mine of information and assistance on vaccine and vaccination issues. She is an ally and a resource of great value.
Barbara’s latest commentary on the corrupt – and corrupting – vaccine industry is a very important read.
In it she points out that vaccine safety and effectiveness have not been demonstrated by the studies published about them even in prestige journals. Those studies are of poor quality and show little that can be relied upon scientifically, but are, none the less, used as the evidence relied upon by vaccine courts to determine whether vaccines have harmed or killed anyone.
The Natural Solutions Foundation has filed a Citizens Petition with the Federal Trade Commission demanding hearings on whether vaccines are safe and/or effective and asking for a ban on any advertising or materials which suggest that they are either safe, effective or both until that fact is established.
And click here (http://drrimatruthreports.com/?p=2220) to read the latest news on the “accidental” Baxter International contamination scandal in which live, virulent Avian Flu H5N1 virus was somehow mixed with seasonal flu vaccine shipped to 18 countries. This mixture would allow re-assortment or mutation of the Avian Flu virus which currently is very ineffective in causing human disease. Such alteration of the virus could potentially allow it to become as deadly as the Avian Flu has been predicted to be when it causes the next “inevitable” pandemic. Of course, if it is mixed in with other flu viruses and injected “by accident”, the next pandemic really IS inevitable.
Please share this information as widely as possible, and make a tax deductible donation (http://drrimatruthreports.com/?page_id=189) as generously as possible so that the Natural Solutions Foundation can continue to bring you vitally important information and fight for your health and freedom.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
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Vaccine Studies: Under the Influence of Pharma
Barbara Loe Fisher
If you take more than a casual look at the way the mass vaccination system in the U.S. works, you see that pharmaceutical companies marketing vaccines have a lot of clout.
It was the pharmaceutical industry that told Congress in 1982 that they were going to leave the nation without vaccines if they didn’t get liability protection but have opposed making it less difficult for vaccine victims to obtain federal compensation in the U.S. Court of Claims under a 1986 law that gave them liability protection.
It is Pharma lobbyists, who bully the FDA into fast tracking vaccines like Gardasil and who sit at the CDC’s policymaking tables urging that new vaccines be recommended for use by all children so they can persuade state legislators to mandate vaccines like influenza vaccine.
How Big Pharma Influences Medical Journals
A recent study published in the British Medical Journal reveals the clout that Big Pharma has in the world of medicine journal publishing, specifically the publishing of scientific articles about vaccines. In a Cochrane Collaboration review and analysis of published influenza vaccine studies found that influenza vaccine studies sponsored by industry are treated more favorably by medical journals even when the studies are of poor quality.
This analysis confirms that drug companies marketing vaccines have a major influence on what gets published and is said about vaccines in medical journals. It is no wonder that there are almost no studies published in the medical literature that call into question vaccine safety.
The preferential treatment of Pharma-funded studies also explains why the risks of an inappropriately fast-tracked vaccine like Gardasil are underplayed in the medical literature and why a physician like Andrew Wakefield, M.D. who dared to publish a study in 1998 in a medical journal (The Lancet) calling for more scientific investigation into the possible link between MMR vaccine and regressive autism, has been mercilessly persecuted for more than a decade, by both Pharma-funded special interest groups, as well as public health officials maintaining close relationships with vaccine manufacturers.
Study Finds No Correlation Between Quality of Study and Publication
This recent review identified and assessed 274 published studies on influenza vaccines for their methodological quality and found no relationship between study quality, publication in prestige journals or their subsequent citation in other articles.
The researchers also found that most influenza vaccine studies are of poor quality but those with conclusions favorable to influenza vaccinations are of significantly lower methodological quality. The single most important factor determining where the studies were published or how much they were cited was sponsorship, with those partially or wholly funded by the pharmaceutical industry having higher visibility.
The authors commented: “The study shows that one of the levers for accessing prestige journals is the financial size of your sponsor. Pharma sponsors order many reprints of studies supporting their products, often with in house translations into many languages. They also purchase advertising space in the journal. Many publishers openly advertise these services on their website. It is time journals made a full disclosure of their sources of funding”.
The HPV Vaccine — Just One Example of Inappropriate Influence Endangering Public Health
Last month the National Vaccine Information Center (www.NVIC.org) called on the Obama Administration and Congress to investigate Gardasil vaccine risks. NVIC has long questioned the inappropriate influence of vaccine manufacturers in federal vaccine licensing and policymaking and state vaccine mandates.
In 2006, Merck’s Gardasil vaccine was fast tracked by the FDA at Merck’s request and in 2007 Merck lobbyists mounted an aggressive lobbying campaign to get Gardasil mandated by state legislators for all sixth grade girls, which would have assured the big drug company a predictable market.
The Pharma lobbying effort in 2007 to get all states to mandate Gardasil failed but every other vaccine produced by drug companies and licensed by the FDA in the past quarter century has been mandated. Those new mandates were added to state vaccine laws by legislators and public health officials at the urging of vaccine manufacturer lobbyists and Pharma funded organizations touting vaccine studies published in the medical literature.
Massive Increase in Number of Vaccines Given
In the past three decades, the numbers of doses of government recommended vaccines for children and medical organizations like the American Academy of Pediatrics has tripled to 69 doses of 16 vaccines, with 48 doses of 14 vaccines targeted to children under age six.
Pharma lobbyists have persuaded most states to pass laws requiring two to three dozen doses of most of the 16 government recommended vaccines. Last year New Jersey became the first state to mandate influenza vaccine for children attending daycare and school.
In the past few years, Dr. Jefferson has authored several independent reviews of influenza studies published in the medical literature for the Cochrane Collaboration, which have been published in the British Medical Journal, questioning the quality of published scientific evidence for influenza vaccine effectiveness and safety for the elderly as well as children.
Clearly, if the makers and marketers of vaccines can influence the quality and quantity of the scientific evidence published in the medical literature proving that vaccines are safe and effective — evidence that is used by states to mandate vaccines and by the U.S. Court of Claims to deny compensation to vaccine injured children — then Congress was wrong in 1986 to protect the makers and marketers of vaccines from liability for injuries and deaths caused by those vaccines.
Government Vaccine Recommendations Based on Tainted Evidence
The U.S. Court of Claims vaccine injury compensation awards, and state vaccine mandates are justified on the strength of scientific published in medical journals. It is time for medical journals to disclose all financial ties to the pharmaceutical industry. It is time for studies questioning the safety and effectiveness of vaccines to receive a fair hearing in scientific journals rather than editors confining themselves to primarily publishing studies funded by the pharmaceutical industry maintaining that every vaccine is totally safe, effective and necessary.
Kudos to the British Medical Journal for having the integrity to publish Dr. Jefferson’s comprehensive analysis of pharmaceutical money influence on vaccine studies published in the medical literature. Hopefully, this will be a wake-up call for the scientific community, Congress and the public to put an end to the undue influence the pharmaceutical industry has on the science and policy of mass vaccination in the U.S.
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Click here (http://salsa.democracyinaction.org/o/568/t/112/campaign.jsp?campaign_KEY=26405) to tell Congress to divest the corrupt and inefficient FDA and USDA of their food regulatory responsibilities before they kill more of us!
In the last in a long, long string of documented failures, shortcomings and tragic errors by the FDA, a recent report documents that the FDA is not only prejudiced and biased, but so riddled with conflits of interest, now not even considered a problem at the failed agency, that there is no way to trust the honesty or accuracy of the decisions of the agency.
While this study looks at one aspect of the impact on drug regulation, food regulation is the same, only worse.
There, the same problems apply, along with the intentional down-regulation of food to support the pharmaceutical markets which profit from the poor drugs approved by the drug regulatory side of the FDA house since degraded food makes people sicker quicker, and makes the profit picture derived from the drugs to treat those illnesses stronger longer.
The picture is a dismal one but there is at least one solution: divest the FDA (and its equally corrupt partner in food crime, the USDA) of all food responsibilities. Rather than creating an new agency, as is currently being discussed by Congress, which will not deal with the fundamental issues and their deadly consequences, the answer, be believe, is to divest the Federal Government of all food regulatory responsibility and instead turn those responsibilities over to the unit of government which the people can impact: State governments.
This is an urgently important concept and must be enacted, even as numerous States are asserting their soverignty from the corrupt and dangerous United States.
Please support the Natural Solutions Foundation in its efforts to make food save once again, protecting food and freedom.
You can donate to the Natural Solutions Foundation at http://drrimatruthreports.com/?page_id=189. All US donations are tax deductible.
Spread the word and ask everyone you know to join the Health Freedom eAlerts, http://drrimatruthreports.com/?page_id=187, for up to the minute information and Action Items.
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Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
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FDA Not Effectively Monitoring Investigator Conflicts of Interest, HHS Watchdog Says
Neil Osterweil
Information from Industry
Assess clinically focused product information on Medscape.
Click Here for Product Infosites – Information from Industry.
January 16, 2009 — More than one third of new drug marketing applications approved by the US Food and Drug Administration (FDA) were missing information about potential conflicts of interest for clinical trial investigators, which could allow bias to creep into the approvals process, a government report released this week has found. The FDA has said that it agrees with most of the report’s findings.
Federal regulations require clinical trial sponsors to collect financial information from investigators at the outset of trials, and to report on their efforts to minimize the possibility that financial self-interest could color trial results, notes the report from the office of Daniel R. Levinson, Inspector General of the Department of Health and Human Services (HHS).
Trial sponsors — usually the company developing or licensing the drug or device in question — only have to disclose this information when they apply for marketing approval, and even then there’s a loophole: they can claim that they “acted with due diligence” to collect financial information from each investigator to satisfy regulations.
Report Found Few Financial Disclosures
Yet 42% of new drug marketing applications filed in fiscal year 2007 were short on investigator financial disclosures, and in fully one fifth of cases where such information was disclosed, FDA reviewers took no action, the watchdogs reported.
“In FY 2007, only 1% of clinical investigators disclosed a financial interest,” the report’s authors write. “By way of comparison, the Journal of the American Medical Association reported that between 23% and 28% of academic researchers had financial interests in medical companies. Further, we found a number of limitations in FDA’s oversight, leaving FDA unable to determine whether sponsors submit financial information for all clinical investigators.”
In addition, the HHS inspector general’s staff found that FDA can’t verify whether relevant information has been collected on all investigators because of incomplete data and the lack of on-site verification procedures.
Collection and review of such information should be routine, as should appropriate action when required, and all of it should occur before a trial ever gets off the ground, contends a former FDA reviewer interviewed by Medscape Medical News.
“You want to intervene at a time when there’s an ability to do something about it,” said John H. Powers III, MD, now an assistant clinical professor of medicine at the George Washington University (GWU) and University of Maryland Schools of Medicine.
“To have a situation where the sponsor has already done the trial, submits the information, and then the FDA says ‘you have conflicts of interest with your investigators,’ puts the sponsor in a bad spot, the investigator in a bad spot, and it puts the FDA in a bad spot. It seems to me that if you’re going to regulate here that you should do it a proactive manner,” he said.
“Management Failure”
Federal regulations concerning drug marketing approvals require that “adequate measures are taken to minimize bias on the parts of the subject, observers, and analysts of the data,” Dr. Powers noted, yet one of the most common sources of potential bias — investigator relationships with industry — are overlooked or ignored.
“This is a management failure,” said David B. Ross, MD, PhD, a former FDA reviewer who is now a clinical assistant professor at GWU. “The managers who have set this policy have done nothing to enforce it and there are no consequences, and the reason is that nobody thinks it matters; they’re kind of doing this for show.”
When Dr. Ross was at the FDA, he and other reviewers warned agency management that a study used to support approval of the antibiotic telithromycin (Ketek, sanofi aventis) was marred by per-patient payments to investigators of up to $400, and, in at least one case, by fraud on the part of the investigator who enrolled the most patients (she was later sentenced to 57 months in federal prison), and by “serious violations in trial conduct” in 9 other trial sites, leading to 4 referrals for criminal investigation.
Despite the warning, and despite ongoing concerns about reported hepatotoxicity from the drug, FDA management failed to take substantive action in response to reviewer concerns, a failure that Dr. Ross said is emblematic of the agency’s apparent indifference to the possible influence of investigator financial relationships with industry.
“…CDER [the Center for Drug Evaluation and Research] is not doing that good of a job, and with what they do track, what are they doing with it? It’s like having laws against speeding and not writing any tickets,” Dr. Ross said.
Relationships Can Have Profound Effect
Eric G. Campbell, PhD, an associate professor at the Institute for Health Policy and the Department of Medicine at Massachusetts General Hospital and Harvard Medical School in Boston, said that financial considerations — whether honoraria, consulting fees, stock options, or direct payments — can have a profound effect on which trials get published or promoted.
“The important thing to remember is that relationships with industry — they may not always be conflicts — are ubiquitous in all aspects of medicine, medical research, and medical regulatory affairs,” Dr. Campbell said. “If a study is funded by a drug company to investigate its product and if the investigator also has relationships with that company, you can be darn sure that if the study makes it to publication, it’s going to favor that product,” he said.
Like Dr. Ross and Dr. Powers, Dr. Campbell pointed out that lax or absent regulatory oversight implies a lack of concern and a tacit acknowledgment of a lack of enforcement of existing rules.
“The bottom line is that if you don’t report stuff and nobody pays attention to whether it’s reported or not, you’re just signaling that it’s not important and that nobody cares, and clearly that’s the message that FDA is sending out,” he told Medscape Medical News.
Key Findings
The report, prepared by staff from the Chicago regional Office of Evaluations and Inspections in the HHS Inspector General’s Office, was based on reviews of financial forms, attachments, and accompanying FDA review notes for all 118 marketing applications approved by the agency in fiscal year 2007. The watchdogs also reviewed FDA regulations and guidance, conducted structured interviews with FDA officials, and surveyed FDA reviewers.
The key findings were:
* 1% of clinical investigators (206 of 29,691) disclosed a financial interest.
* FDA does not have a complete list of clinical investigators and does not use on-site inspections to confirm that submitted financial information is complete, meaning that reviewers cannot determine whether sponsors have submitted financial information for all clinical investigators
* 42% of FDA-approved marketing applications were missing financial information, 23% of approved marketing applications were missing a certification or disclosure form or required attachments, and in 28% of applications, sponsors used the due-diligence exemption to indicate that they were unable to provide complete financial information.
* FDA did not document a review of any financial information for 31% of marketing applications. Reviewers who followed a review template were more likely to include financial information than those who did not.
* In 20% of applications with disclosed financial conflicts, neither the FDA nor sponsors took action.
The Inspector General’s recommendations for the FDA were as follows:
* Ensure that sponsors submit complete financial information for all clinical investigators.
* Use a complete list of clinical investigators to check that sponsors have submitted financial information for all.
* Require that sponsors submit financial information for clinical investigators as part of the pretrial application process.
* Check that sponsors have submitted all required attachments to financial forms.
* Update guidance to sponsors regarding the due-diligence exemption.
* Add a review of financial information to the on-site inspection protocol.
* Ensure that reviewers consistently review financial information and take action in response to disclosed financial interests.
* Require that all centers consistently use a template that includes a prompt to document a review of financial information.
* Provide additional guidance and training to reviewers.
FDA Replies
In response to a request from Medscape Medical News for comment, FDA spokesperson Karen Riley sent a statement noting that the agency agreed with all of the HHS recommendations except the one stating that the FDA should request information from clinical investigators prior to trial initiation.
“The intent of clinical investigator financial disclosure is not to discourage investigators from being included in the study,” the FDA response says. “Rather, it allows sponsors to identify and manage potential conflicts throughout the development of a regulated product, from design through the conduct of the clinical trials.”
The statement goes on to say that this recommendation for financial disclosures before trial initiation could needlessly add to “the complexity and cost of the clinical trial enterprise with no commensurate gain in the protection of human subjects or the quality of the data.”
This pretrial disclosure recommendation is not meant to be punitive or burdensome, Dr. Powers said, but it recognizes the fact that bias, whether intended or not, can slip into the process whenever money is involved.
“When people bristle at regulations, I always think of James Madison’s quote,” he remarked. “Madison said that ‘If all men were angels, no government would be necessary.’ The reasons why we do these things is not because everybody is inconsistent or immoral: it’s because some people are. It seems onerous to people who have no intention of doing the wrong thing, but unfortunately these rules are written for people who aren’t going to do the right thing.”
http://www.medscape.com/viewarticle/586980?sssdmh=dm1.423642&src=nldne