Posts Tagged ‘health freedom’

GM Files: GMIs – Genetically Modified Insects

Thursday, October 23rd, 2008

I am nearly speechless by the stupidity and ill-conceived arrogance of industry scientists who are playing havoc with my world and yours.
Read this for yourself and see if you do not believe that you need strong allies to fight this madness back into the nightmare it came from.
That ally is the Natural Solutions Foundation. Give us the voice and give us the strength to carry this battle forward by making sure that you are on the distribution list of the free Health Freedom eAlerts (sign up on our home page, www.HealthFreedomUSA.org) and by forwarding the eAlerts to your entire list and asking them to take the action steps therein.
This madness MUST stop.
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.Organics4U.org
www.NaturalSolutionsMarketPlace.org
www.NaturalSolutionsMedia.tv

Invasion of the warrior insects
Clive Cookson
Financial Times, October 11 2008

Scientists are about to unleash a new weapon in mankind’s running battle
against insect pests: a genetically modified flying army. The first
commercial release of GM insects, to protect US cotton fields from the
voracious pink bollworm, is expected within the next two years. The second
target will be the mosquito that spreads dengue fever in Asia.

This new airborne offensive is being mounted from a business park near
Abingdon, Oxfordshire, where a set of low-key laboratories houses the
world’s leading centre for GM insect development. Oxitec, a private company
spun out of Oxford University in 2002, holds tens of thousands of moths,
mosquitoes and flies in its insectaries. They are undergoing genetic
engineering as part of the fight against agricultural pests and carriers of
human disease.

GM is being deployed to extend the “sterile insect” technique that has
already successfully eradicated pests such as screw-worms and Mediterranean
fruit flies (medflies) in parts of north America. The idea is that vast
numbers of sterile yet virile males – at least 10 times as many as the wild
population – are released in infected areas. These sterile newcomers swamp
the native males, mating with all available females, which then fail to
produce any offspring.

Until now, insects have been sterilised before release by old-fashioned
irradiation from radioactive isotopes. But this is a crude technique that
works only on some species. “It doesn’t work for mosquitoes because a
radiation dose big enough to sterilise the insect will also incapacitate or
kill it,” says Luke Alphey, founder and research director of Oxitec.

With colleagues at Oxford University he discovered how to achieve the same
effect more gently and specifically, by inserting a “dominant lethal” gene
into the insects. “The males produce viable sperm which will fertilise the
egg, but the embryo [larva] dies in development,” says Alphey, who left the
university this year to work full time for the company.

“Of course the system needs to be reversible, so that we can breed the
insects in the first place,” he adds. This is achieved by designing the
lethal gene so that it can be suppressed by adding the antibiotic
tetracycline to the captive insects’ diet. In the absence of tetracycline,
the larvae die.

The lab insects live in clear plastic containers of various shapes,
typically about the size of an archive box. Some have fine mesh or gauze on
one side. Fruit flies, for example, lay their eggs on the mesh, where they
can easily be collected by lab staff.

Female mosquitoes receive what’s known as their “blood meal”, which they
need to breed, through the gauze. Genevieve Labbe, who is in charge of the
mosquito breeding programme, gives them horse blood heated to 37Æ’C, twice a
week. “First we blow into the cage to tell them there’s something to bite,”
she explains. Carbon dioxide in the breath alerts the insects to the
presence of a warm-blooded animal.

The mosquitoes, which have been sitting or flying lethargically around their
box, begin buzzing energetically in response to Labbe’s breath. Then a
cylinder of warm blood, with one end covered with sausage skin, is placed
against the gauze – and the mosquitoes gorge themselves.

Oxitec’s highest-profile project is to attack Aedes aegypti mosquitoes, the
carriers of dengue fever, which afflicts an estimated 100m people every
year. The work is funded with a $5m grant from the Bill & Melinda Gates
Foundation, part of the charity’s drive to reduce the toll from tropical
diseases.

“Both the incidence and severity of dengue are increasing,” warns Alphey.
“There are no drugs or vaccine, and $1bn has been spent – largely
ineffectively – on dengue control through insecticide fogging and site
sanitation.” (The mosquitoes breed in small rainwater pools, such as those
that form in discarded tyres.)

The Malaysian government is collaborating with Oxitec to run a field trial
with GM insects on Pulau Ketam, an island east of Kuala Lumpur inhabited
mainly by Chinese fishing families. Its relative isolation makes Pulau Ketam
a good test site, because were Aedes aegypti to be suppressed locally, the
success would not be masked by mosquitoes moving in from elsewhere. But some
residents are objecting to what they call “warrior” mosquitoes.

“What else will the ‘warrior’ mosquitoes kill?” asked Saw Lek, a retired
teacher quoted in the South China Morning Post. “We fear, once released,
there is no way to control the new mosquito if anything goes wrong.”

There are also objectors further afield. Mae-Wan Ho, director of the
Institute of Science in Society, based in London, calls the use of
“terminator mosquitoes” to control dengue “dangerous and costly”. She
believes there is a risk of the lethal genes moving from the released GM
mosquitoes into other organisms and disrupting the already fragile
environmental balance.

But Oxitec scientists insist their GM mosquitoes are environmentally benign.
First, they argue, only the non-biting males are released; they are easily
sorted from the females in the breeding facility because their pupae are
smaller.

“The natural population density of Aedes aegypti is not high,” says Alphey.
“For a city of 1m people you are probably talking about releasing 10-20
mosquitoes per person per week. I don’t think anyone would notice the
increase in the mosquito population.”

He points out too that Aedes aegypti, like the other pests targeted by
Oxitec, is not a native species (it originates in Africa) but has been
spread around the world by human activities. Its eradication would not
disrupt any local ecosystems. “There is no breeding route into a wild
population,” Alphey insists. And if the terminator gene does inadvertently
get into wild mosquitoes, it “absolutely will not spread”, because any
insects carrying it would not survive.

The promise to keep genetic modification out of the wild population may make
the Oxitec technology more acceptable to sceptics than other ways of using
GM insects, which are being studied but are further from commercial
application. Scientists at Imperial College London, for example, plan
permanently to change the genetic make-up of wild mosquitoes, so that they
can no longer transmit a human pathogen such as the malaria parasite.

Safe or not, GM technology will get nowhere without winning over the people
living near release sites, warns Anthony Wilson, an expert on insect-borne
disease at the UK-based Institute of Animal Health. “If you can see a
facility releasing clouds of mosquitoes, you’ll want to be very sure that
you are not just being used for experimental purposes,” says Wilson. In the
1970s, long before scientists could genetically engineer insects, the World
Health Organisation and the Indian government had to cancel an ambitious
dengue control project after local newspapers caused a furore with erroneous
claims that it was a camouflaged US germ warfare experiment.

In the US, Oxitec’s pink bollworm project is not meeting hostility, partly
because American public opinion is less suspicious of genetically modified
organisms than Asian and European. Another reason is that the GM insects
released in the US would replace insects sterilised by irradiation in the
fight against cotton bollworm, rather than adding millions of new insects to
the existing population. “We have had three years of field trials, releasing
our GM pink bollworm from the air over cotton in Arizona,” says David
Brooks, Oxitech chief executive. “We had a very positive environmental
impact report [from the US Department of Agriculture] and we could go into
commercial operation next year or in 2010.”

A bigger prize in the agricultural sector would be the medfly, a scourge of
fruit-growers worldwide. Oxitec hopes the US government will eventually
adopt GM technology to replace the irradiation facilities that it is funding
in central America to push medfly further away from the US. The
sterilisation plant in Guatemala produces a staggering 2bn sterile flies
every week – that’s 20 tonnes of living insect.

Once the GM medflies have proved themselves in field trials, the US
authorities, nervous about the potential security risks posed by radioactive
sources, may indeed prefer the cleaner and simpler technique of genetic
sterilisation. But it is hard to imagine GM insects being released in
Britain or Europe for the foreseeable future. If activists are determined to
trash static biotech crops, imagine the uproar that would greet GM on wings.
Clive Cookson is the FT’s science editor.
http://www.gmfreeireland.org/news/index.php

Evidence of poison: New Levels of Compulsory Drugging – MSG Sprayed on Your Food!

Thursday, October 23rd, 2008

There are two articles which follow this introduction which have great bearing on your health and, eventually, your ability survive.
Agricultural chemicals have been known since their inception to pose significant threats to human, animal and environmental health. They are, in fact, only approved for use on the food supply of people and animals because, in my opinion, of the enormous wealth which chemical companies, which are, in essence, a branch of the pharmaceutical industry, have have available to throw at compliant regulators and legislators, plus deceptive and misleading advertising bulwarked by corporate junk science.

Agricultural chemicals are not, however, limited to herbicides, fungicides, pesticides and fertilizers. Other chemicals quality for that designation, too. For many years, the US has permitted the spraying of fluoride and mercury on crops after harvest to prevent mold growth during storage despite the well characterized dangers of those substances.
Now, another toxin, also well known for its adverse effect on the brain, the nervous system, the endocrine system, perception, mood and vascular integrety has been approved by the supposed guardians of our health, the FDA, EPA and USDA for direct application, without any upper limit, on our foods.

Read this article and ask yourself whether you ever want to eat non organic food again. Then ask yourself why regulators are permitting known toxins in our food.

And then click on this link (https://www.staging.healthfreedomusa.com/index.php?page_id=189) to make a donation to the Natural Solutions Foundation, a totally donation-supported Non governmental organization (NGO) devoted to your right to make your own choices in your health. Among the freedoms that we believe belong to you and that we are fighting for on your behalf, and ours, is the right to know what your food has been sprayed with, genetically modified with, contaminated with or irradiated with. In short, if food is contaminated you have a right to know it.
And you have another right, too, as I see it.
You have a right to be protected by the regulators from the self-interested companies that do not care at all about the damage their chemicals and processes bring to you and yours. That is, after all, what we believe regulatory agencies are supposed to do. But the sad truth is that we need to be protected FROM the regulatory agencies.
That’s one of the things that Natural Solutions Foundation does, in fact. And, of course, we need your help. Click here (https://www.staging.healthfreedomusa.com/index.php?page_id=189) to become a supporting sponsor with a tax deductible recurring donation. And visit the Natural Solutions Foundation home page, www.HealthFreedomUSA.org, to sign up for our free, secure Health Freedom eAlerts.

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.Organics4U.org
www.NaturalSolutionsMarketPlace.org

MSG is being sprayed right on fruits, nuts, seeds, grains, and vegetables as they grow —
even those used in baby food

In the 1970s, reluctant food processors “voluntarily” took processed free glutamic acid (MSG) out of baby food. Today it’s back, in fertilizers called “Omega Protein Refined/Hydrolyzed Fish Emulsion” and “Steam Hydrolyzed Feather Meal,” both of which contain hydrolyzed proteins; and in a product called AuxiGro WP Plant Metabolic Primer (AuxiGro) produced by Emerald BioAgriculture (formerly Auxein Corporation), which contains both hydrolyzed protein(s) and “monosodium glutamate.” AuxiGro is being sprayed on some of the vegetables we and our children will eat, into the air we and our children must breath, and onto the ground from which it can move into drinking water. Head lettuce, leaf lettuce, tomatoes, potatoes, and peanuts were among the first crops targeted. On September 12, 2000, the Auxein Corporation Web site gave the following information:

Crops registered include: Celery; Fresh Market Cucumbers; Edible Navy and Pinto Beans; Grapes; Bulb Onions; Bell, Green and Jalapeno Peppers; Iceberg Head Lettuce; Romaine and Butter Leaf Lettuce; Peanuts; Potatoes; Snap Beans; Strawberries; Processing Tomatoes; Fresh Tomatoes; and Watermelons.

Today, there is no crop that we know of that has not been approved for treatment with MSG by the U.S. Environmental Protection Agency (EPA).

Even in California — the only state where there are any restrictions on the use of AuxiGro — AuxiGro has been approved for use on a number of crops, and Emerald BioAgriculture continues to push for more. Field tests in California have been — and may continue to be — conducted on a variety of crops, and those AuxiGro treated crops may be sold in the open market without revealing that they have been treated. We can’t tell you which crops those are because the CDPR has refused to send records of test trials (which are public information) to the Truth in Labeling Campaign.

As of June 13, 2002, AuxiGro was registered for use in California on tomatoes, almonds, apricots, cherries, plums, nectarines, peaches, prunes, grapes (including grapes to be used in wine), and onions. At that time, the California Department of Pesticide Regulation said they were not aware of any testing of AuxiGro for use on other crops. They also said that they did not have any proposals presently in house to register additional crops for AuxiGro. It would appear, however, that what the CDPR said was not true, for the CDPR subsequently announced that Emerald BioAgriculture had applied for permission to use AuxiGro on tomatoes (new use), and on melons (new crop) — and, to the best of our knowledge, approval is always preceded by field testing.

On July 7, 2004, Emerald BioAgriculture requested approval of use of AuxiGro as a desiccant, disinfectant, fertilizer, fungicide, growth regulator – for increased yield and prevention of powdery mildew in various crops such as almonds, grapes, and melons. They also asked to add cole crops (including broccoli, brussels sprouts, cabbage, cauliflower, kale, collards, turnips, rutabaga, mustard, watercress, and kohlrabi) to the list of crops approved for AuxiGro use.

Approval for use on organic crops–in all states–has been requested.

What’s wrong with using glutamic acid, an amino acid found in protein, as a spray on crops?

– In protein, amino acids are found in balanced combinations. Use of free glutamic acid as a spray on crops throws the amino acid balance out of kilter.

– It’s not the glutamic acid found in protein that is being sprayed on crops, it’s a synthetic product. The spray being used most widely is called AuxiGro. The “free glutamic acid” or so called “L-glutamic acid” component being used by its manufacturer, Emerald BioAgriculture, contains L-glutamic acid, an amino acid found in protein; but it also contains D-glutamic acid, pyroglutamic acid, and other chemicals referred to in the industry as “contaminants.” The free glutamic acid used in AuxiGro is processed free glutamic acid. It is manufactured — in chemical plants — where certain selected genetically engineered bacteria — feeding on a liquid nutrient medium — excrete the free glutamic acid they synthesize outside of their cell membrane into the liquid medium in which they are grown. In contrast, the free glutamic acid found in protein, and the free glutamic acid involved in normal human body function, are unprocessed. free glutamic acid, and contain no contaminants.

– No one knows what the long term effects of spraying processed free glutamic acid on crops will be.

– That the processed free glutamic acid (MSG) will be absorbed into the body of the plant and into the fruit, nuts, seeds, or vegetable it produces seems undeniable. If it were not, the plant would not be stimulated to grow. Neither Emerald BioAgriculture or the EPA will address this issue.

– That there will be residue left on crops has not been disputed by Emerald BioAgriculture. But no study of either the amount of that residue, or the least amount of processed free glutamic acid needed to cause a reaction in an MSG-sensitive person, has ever been done. “It should wash off” doesn’t mean it will wash off. “It seems unlikely that such a small amount would cause a reactions” doesn’t mean that a small amount will not cause a reaction or have long term health effects.

– Free glutamic acid is known to be toxic to the nervous system. But the neurotoxic effects that processed free glutamic acid will have on animals that consume the plants on which it is sprayed – effects over and above any effects caused by external glutamic acid residue – have never been evaluated. Neither are there data on the effects that spraying processed free glutamic acid will have on drinking water.

– Consider, also, that children are most at risk from the effects of processed free glutamic acid. Their undeveloped blood-brain barriers leave them most at risk from exposure to processed free glutamic acid. It has been repeatedly demonstrated that infant animals fed processed free glutamic acid when young develop neuroendocrine problems such as gross obesity, stunted growth, and reproductive disorders later in life, and that they also develop learning disabilities. Emerald BioAgriculture did not address that particular safety issue in its application to the EPA.

– No one knows how little glutamic acid is needed to kill a single brain cell or to trigger an adverse reaction.

– Free glutamic acid is a neurotransmitter. It causes nerves to fire, carrying nerve impulses throughout the nervous system.

– Free glutamic acid is a neurotoxin. Under certain circumstances, free glutamic acid will cause nerves to fire repeatedly, until they die.

– Processed free glutamic acid kills brain cells. The free glutamic acid ingested by laboratory animals that caused brain lesions and neuroendocrine disorders was very often given in the form of the food ingredient “monosodium glutamate.” “Monosodium glutamate” is the name of a particular food additive. Processed free glutamic acid is the reactive component in “monosodium glutamate,” just as processed free glutamic acid is a reactive component in AuxiGro.

The glutamate industry research done in the 1970s that was submitted to the EPA by the Auxein Corporation, that pretended to find that processed free glutamic acid is “safe,” has been long refuted by independent scientists. Indeed, at the present time, neuroscientists attempting to develop drugs to block the toxic effects of free glutamic acid are using processed free glutamic acid to selectively kill certain kinds of brain cells.

– Processed free glutamic acid causes neuroendocrine disorders in maturing animals that ingest processed free glutamic acid early in life.

– Processed free glutamic acid causes learning disorders in maturing animals that ingest processed free glutamic acid early in life.

– Processed free glutamic acid crosses the placental barrier and causes learning disabilities in animal offspring of dams that ingest it.

– Processed free glutamic acid has access to the brain through the blood-brain barrier, which is not impervious to the unregulated flow of processed free glutamic acid. The blood-brain barrier is immature at birth and may continue to develop up to puberty. In certain areas called the circumventricular organs, the blood barrier is never impervious to the unregulated flow of free glutamic acid. In addition, the blood-brain barrier is easily damaged by such events as high fever, a blow to the head, drug use, stroke, ingestion of processed free glutamic acid, and the normal process of aging.

– The National Institutes of Health recognize glutamic acid as being associated with addiction, stroke, epilepsy, degenerative disorders such as Alzheimer’s disease, Parkinson’s disease, and ALS, brain trauma, neuropathic pain, schizophrenia, anxiety, and depression.

– For years, free glutamic acid has been produced and used in food additives with names such as monosodium glutamate, sodium caseinate, and hydrolyzed soy protein. In some people, the processed free glutamic acid in food additives causes adverse reactions that include migraine headache, asthma, arrhythmia, tachycardia, nausea and vomiting, depression, and disorientation. The processed free glutamic acid in prescription and non-prescription drugs, food supplements, and cosmetics can also cause adverse reactions.

There are badly flawed industry-sponsored studies that have pretended to find that processed free glutamic acid does not cause adverse reactions. Inappropriate procedures used by the glutamate industry have included limiting subjects to people virtually guaranteed not to be sensitive to processed free glutamic acid, and/or using processed free glutamic acid or other similarly reactive substances in placebos as well as in test material. The Food and Drug Administration (FDA) has based its claim that processed free glutamic acid causes only mild and transitory reactions on those badly flawed industry-sponsored studies.

– Even the EPA admits that the food additive called “monosodium glutamate” causes adverse reactions.

– Even the FDA admits that the food additive “monosodium glutamate” contains processed free glutamic acid.
<>– Even the FDA admits that many consumers refer to all free glutamic acid as “MSG.”

The EPA’s approvals of use of MSG in agriculture are simple, straightforward, and in violation of the Federal Food, Drug, and Cosmetic Act

In reviewing the application of Auxein Corporation (now Emerald BioAgriculture) for use of processed free glutamic acid in a spray to be applied to crops as they grow, the EPA failed to conform to the requirements of the Federal Food, Drug and Cosmetic Act, which require, in part, that the EPA review any proposed action for validity, completeness, reliability, and relationship to human risk. The EPA also ignored Executive Order 13045 which requires government agencies to consider available information concerning the variability of the sensitivities of major identifiable subgroups of consumers, including infants and children. For example, Auxein Corporation sent the EPA 14 industry-sponsored toxicological studies from the literature, all done in the 1970’s, but failed to mention hundreds of studies in the literature that refuted those 14 studies. Auxein Corporation even failed to send the EPA independent studies that appeared in the same book(s) as the industry-sponsored studies sent to the EPA. For example, although processed free glutamic acid causes brain lesions and neuroendocrine disorders in infant animals, this special hazard faced by infants was ignored by Auxein Corporation. It would appear that Auxein Corporation restricted its consideration of “available information” to information made available by the glutamate industry; and the EPA, even after having been sent abstracts from other “available information,” has not challenged the Auxein Corporation applications. A more complete discussion of the shortcomings of the EPA approvals granted to Auxein Corporation has been submitted to the EPA.

Questions about the safety of spraying processed free glutamic acid on plants and into the environment have been raised by the Truth in Labeling Campaign and by individual consumers. The EPA has refused to address those concerns. The EPA, and, in particular, EPA spokesperson Dr. Janet Andersen, has failed to respond to allegations that in approving the spraying of processed free glutamic acid, the EPA failed to consider the reliability, validity, and completeness of the Auxein Corporation application or comply with Executive Order 13045 entitled Protection of Children from Environmental Health Risks and Safety Risks, except to say that the EPA had complied with executive order 13045. Moreover, while responding to letters that asked direct questions of the EPA, Andersen failed to respond to most, if not all, of the direct questions contained in those letters.

AuxiGro, the first MSG-laced plant “growth enhancer” to hit the market, has been approved for spraying on every crop we know of, with no restrictions on the amount of processed free glutamic acid (MSG) that may remain in and/or on crops when brought to market. Even before consumers had an inkling that crops were being sprayed, the Truth in Labeling Campaign received reports that MSG-sensitive consumers had gotten sick from head lettuce and potatoes.

Federal Register notices chronicling the application and approval of processed free glutamic acid are available on the Web via GPO Access, the Federal Register, through: http://www.gpoaccess.gov/fr/index.html. Application for approval of use of AuxiGro was made to the EPA in 1997. Testing of the product was also approved in that year, and many of the test crops sprayed with AuxiGro were brought to market without notifying consumers. Glutamic acid was granted an exemption from establishment of a tolerance limit in January, 1998. AuxiGro was also approved for use on a number of crops in January, 1998, and approved for use on other crops later. No announcement of these approvals was made in the Federal Register.

Due to a technical glitch in the system, the glutes came to need one more approval to make their California registrations work. The glutes were asking for AuxiGro to be approved for use as a fungicide in California, but the EPA had only approved AuxiGro for use as a pesticide produce or plant growth enhancer. And when application was made for this addition to their approvals, the application was brought to our attention; and the Truth in Labeling Campaign filed a formal protest to this approval of AuxiGro. The Formal Objection of the Truth in Labeling Campaign was filed on August 16, 2001 with the EPA.

By law, formal objections filed in a timely manner must be responded to within six months. Also, by law (we were told) even though the Final Rule had not been promulgated, this additional use of AuxiGro would be considered approved unless and until the EPA determined that it should be otherwise. In July, 2004, we received a conference call from Dr. Andersen and a number of other EPA players, including an EPA lawyer — a “courtesy call” telling us that our objections had been discounted and that the Final Rule allowing use of AuxiGro as a fungicide would be published shortly in the Federal Register.

What’s wrong at the EPA?

Neither the EPA nor Janet Andersen, Ph.D., director of the Biopesticides and Pollution Prevention Division (BPPD), are stupid. Rather, all evidence would appear to suggest that the EPA, which is charged with protecting the health of Americans, says it is protecting the health of Americans, when in fact the EPA acts to protect the bottom line of big business. Don’t think for a moment that MSG is the only toxin unleashed on the American public by the EPA. Let the words “methyl parathion” and “DDT” jog your memory.
The EPA, in granting the chemical referred to as “L-glutamic acid” an exemption from the requirement of a tolerance for residues of “L-glutamic acid” on all food commodities when applied/used in accordance with good agricultural practices (thereby allowing unrestricted amounts of processed free glutamic acid (MSG) residue to remain in and on any and all food crops that come under the EPA’s jurisdiction) violated Section 408(c)(2)(A)(i), Section 408(c)(2)(ii), Section 408(c)(2)(B), and Section 408(b)(2)(D) of the Federal Food, Drug, and Cosmetic Act.

Neither “L-Glutamic Acid and Gamma Aminobutyric Acid; Exemptions from the Requirement of a Tolerance; Final Rule” (Federal Register June 21, 2001) nor “Glutamic Acid; Pesticide Tolerance Exemption; Final Rule” (Federal Register January 7, 1998), which preceded it, met the criteria established by law for granting exemptions from the restriction of a tolerance.
How did spokesperson Andersen excuse the fact that the EPA approved processed free glutamic acid for use in an EPA approved spray? First, said Andersen, the free glutamic acid used in the spray is naturally occurring, and it’s 99.3 per cent pure pharmaceutical grade L-glutamic acid. Yet, in admitting that the free glutamic acid in AuxiGro is not 100 per cent pure L-glutamic acid, and that it is pharmaceutical grade, Andersen contradicted herself, and actually made the point that 1) if the free glutamic acid used in AuxiGro were truly natural, it wouldn’t be “pharmaceutical grade;” and 2) if the free glutamic acid used in AuxiGro were truly natural it would be 100 per cent, not 99.3 per cent pure L-glutamic acid.

Andersen said something else very interesting. She said that the EPA is well aware of the fact that MSG causes adverse reactions. However, when Andersen used the term “MSG” she was referring to the one food ingredient called “monosodium glutamate,” and not to the free glutamic acid in “monosodium glutamate” that causes adverse reactions. Failure to define terms, as Anderson did (and does) so handily, is both deceptive and misleading.

What Andersen did is very clever. What she said makes no sense at all. No one has ever claimed that the processed free glutamic acid in AuxiGro comes out of a box labeled “monosodium glutamate.” So for her to say it doesn’t, is meaningless. On the other hand, the claim has been made that the free glutamic acid in AuxiGro will cause the same brain lesions, neuroendocrine disorders, adverse reactions and other diverse disease conditions that are caused by the free glutamic acid in “monosodium glutamate” and the other food additives that contain processed free glutamic acid. That claim is true, but Andersen does not address it. How do you refute someone who ignores legitimate questions and spews out irrelevant statements as though they pertained to your legitimate questions? You don’t. The EPA defense of its approval of use of processed free glutamic acid in plant “growth enhancers” and its registration of AuxiGro has two parts to it: 1) ignoring those who question EPA actions, and 2) making the irrelevant statement that AuxiGro does not contain MSG (monosodium glutamate).

Neither Andersen nor anyone else at the EPA ever addressed the criticism that approvals given by the EPA to allow the use of free glutamic acid and the product AuxiGro were inappropriate.
The EPA, which approved the used of processed free glutamic acid in plant “growth enhancers,” made a grievous error. But instead of recognizing and remedying that error once it was pointed out to them, the EPA began a cover-up. That cover-up included use of ambiguous words and phrases, half-truths, and downright lies told to consumers. The cover-up continued (and continues still) with a variation of those ambiguous words and phrases, half-truths, and downright lies told to legislators who inquire about spraying MSG into the environment.

You might find the Emerald BioAgriculture sales literature interesting

Sales literature promoting AuxiGro was once found on their Web site, but is now long gone. While Federal Register notices included the fact that there is processed free glutamic acid (MSG) in AuxiGro, the sales literature from Auxein Corporation did not mention the fact that their product contains free glutamic acid until the Truth in Labeling Campaign began to broadcast that information. In November, 1999, Auxein added deceptive, misleading, and untrue statements in an elaboration of its Product Page, wherein they essentially make the untrue assertion that the glutamic acid used in AuxiGro is chemically and biologically identical to that found in plants and animals.

Sales literature did (on September 12, 2000), however, contain the following:

“PRECAUTIONARY STATEMENTS

HAZARDS TO HUMAN AND DOMESTIC ANIMALS – CAUTION”

If you think you might be reacting to AuxiGro sprayed on crops, you might want to try to (contact Emerald BioAgriculture (formerly Auxein Corporation) at the addresses that follow. (A friend recently told us that he tried to contact them by e-mail, but his e-mail was returned unopened.) By law, the company is required to forward reports of adverse reactions to the EPA. You might want to ask the EPA if Emerald BioAgriculture did so.

John L. Mclntyre, Ph.D.
President & CEO
Emerald BioAgriculture (formerly Auxein Corporation)
3125 Sovereign Drive, Ste. B
Lansing, MI 48911-4240
Phone: (888) 828-9346
Fax: (517) 882-7521
E-Mail: mailto:%20sales@auxein.com
(From time to time, their web page, http://www.auxein.com , can be accessed by password only.)

www.Truthout.org

Evidence of poison

Fiona Macleod
08 March 2007 11:59

A Limpopo medical doctor has documented a string of physical abnormalities — including
breasts on a five-year-old girl — that he believes are directly linked to the unregulated
use of agricultural chemicals.

Dr Johan Minnaar (44) has produced evidence of serious illnesses and disorders among his
patients in Groblersdal, where commercial farmers are spraying large amounts of
pesticides on crops.

Horrific cases include teenage boys temporarily “growing breasts” during spraying
seasons, miscarriages, partial facial paralysis, cancers and ear malfunctions. Many of his
patients suffer from milder poisoning symptoms, such as asthma, sinusitis, headaches,
dizziness and depression.

Minnaar, who has been practising as a doctor in Groblersdal since 1997, took the unusual
step of coming forward with his evidence after unsuccessful attempts to get government
and regulatory authorities to intervene.

He said: “Groblersdal is surrounded by farms growing mostly citrus and grapes, but also
cotton, vegetables and maize. Throughout the year there is constant crop spraying with
pesticides containing organophosphates and carbamates. No one has informed the
community what pesticides are being used, even though the law states people must be
notified before spraying.”

Minnaar started investigating after realising that symptoms he had experienced over six
years followed a pattern.

“I experienced chronic fatigue, nausea, muscle aches and pains, skin rashes and arthritis,
particularly from August till November, when there is a noticeable increase in the spraying.
On investigation, it became clear that other people had these symptoms at the same time.”

Last August, he became so ill that he had to stay at home for two weeks. His wife and
three children also showed symptoms. He began regularly testing his and his spouse’s
blood and the tests showed they were exposed to organophosphates and carbamate
pesticides.

Minnaar laid complaints with the registrar of the national agriculture department, the
water affairs department and the labour and health departments of the Limpopo
government. He also tackled the farmers, chemical companies and crop sprayers.

The spraying continued and, on two days in February this year, large amounts of
carbamate were released during the aerial spraying of citrus orchards. Residents were not
warned beforehand. Among those who later showed signs of poisoning were pupils of two
schools located in the orchards.

Minnaar said pupils regularly played on the sports fields during spraying. The teenage
boys who had consulted him about “growing breasts” in the spraying seasons attended the
schools.

In late January, a woman brought a five-year-old girl who had developed breasts to his
consulting rooms. Minnaar suspected it could be linked to poisoning and referred her case
to Limpopo government officials, who he met two days later.

“As with many patients, she had no access to medical facilities or funds. The authorities
undertook to get her medical testing and treatment, but we’ve heard nothing,” he said.

According to Professor Leslie London of the University of Cape Town’s health sciences
faculty, premature puberty and other hormonal abnormalities are symptoms of
contamination by pesticides containing “endocrine disruptors”.

A 2005 study of girls in Mexican farming areas, titled Altered Breast Development in Girls,
indicated that pesticides could affect breast development and lead to early puberty.

Said London: “It has been shown that endocrine disruptors can also affect sexual
maturation and differentiation. A study in Sri Lanka of a pesticide called endosulfan found
that boys living in villages below cashew nut plantations sprayed with endosulfan had
impaired sexual maturity and other reproductive impairments.”

London researched aerial crop spraying around Groblersdal in 2005, with a focus on risks
to small farmers rather than health impacts. Last year, he published research on possible
links between aerial organophosphate spraying in the Northern Cape and Guillain-Barré
Syndrome, a neurological disorder.

“The problem of rural towns affected by agricultural application of pesticides is
ubiquitous,” he said. “Present regulatory and safety management methods really don’t
address this problem sufficiently.

“I think there is a view that if you choose to live in the country, you should accept this as a
way of life. That is a societal value decision, not a matter of science.”

The health department’s directorate of environmental health has announced plans to
launch a chemical safety programme in Groblersdal at the end of March. According to its
draft concept document, “the aim is to launch the programme to inform provinces that
national [government] is willing to assist them in the management of chemicals”.

The draft programme identifies schoolchildren, women, farmers and farmworkers, shack
dwellers, informal traders and manufacturers as the “most vulnerable communities in
municipalities that lack capacity to properly and satisfactorily deal with chemical safety
issues”.

South Africa is a signatory to international conventions aimed at promoting chemical
safety, and the labour ministry said in October that chemical safety was “high on the
minister’s agenda”. But crop spraying is a highly technical industry, and pinpointing
contamination is difficult.

London said it was almost impossible for applicators in planes to control the drift of
chemical sprays. “Aerial application has been shown in some studies to drift more than
2km, even in the absence of strong winds.”

European countries strictly regulate the industry through buffer zones around residential
areas and warning systems, he added.

Gerrit van Vuuren, an aerial application consultant at Croplife South Africa, blamed mist-
spraying of crops on the ground. “It is absolutely wrong to conclude that because there is
a yellow aircraft spraying agrichemicals in an area, it must the reason for ill health effects,”
he said.

Van Vuuren said mist-blowers apply more than 1 000 litres of spray mixture a hectare,
compared to 30 to 40 litres in the case of aerial spraying. They also blow a significant
volume of the spray higher than 6m into the air.

“A couple of mist-blowers spraying thousands of litres of spray mixtures at night are less
visible than an aircraft spraying a couple of hundred litres in the morning.”

He said it was up to farmers to notify inhabitants and issue warnings. They were also
supposed to ensure no one entered their fields during spraying.

The environmental health unit at the Elias Motsoaledi municipality, under which
Groblersdal falls, said it was “busy investigating the usage of pesticides being sprayed
from aeroplanes, as nuisances do occur from these activities”.

But Minnaar is frustrated by government promises to investigate. “For all practical
purposes, the supposed controls are not working. While they keep promising to sort it out,
we are getting poisoned,” he said.

Supplements Are “Dangerous” – Poison Press At Work Again

Tuesday, October 14th, 2008

The Natural Solutions Foundation keeps a close eye on the continuing disinformation of Big Pharma to try to convince you that there is no reason to, or good reason not to, take dietary supplements. It is like Honda telling you that there is no reason to buy, or good reason not to buy, a Toyota.

You see, dietary supplements are the direct economic competitor of drugs. Dietary supplements, like clean, unadulterated food, keep you healthy and get you back to health if you have become ill.

Compared to drugs, they are cheap, safe, easy to use and controllable by you or a helpful nutritionally knowledgeable person. And, at least in the US, they are classified as foods so they cannot be regulated the way drugs would be.

Of course, the FDA is always on the look out to undermine that freedom, recognized by the 1994 Dietary Supplements Health and Education Act (DSHEA) — unanimously adopted by Congress — which this Agency publicly calls “the worst act ever passed by the US Congress”. Why? Because the FDA is run by and for industry and the drug industry is a leading source of FDA funds through User Fees. The big players in the food industry, who pay no user fees to the FDA are, none the less, very important buddies of the organization, so food is regulated for the interests of big industry and drugs are regulated to promote the drug industry, at the expense of anything that might get in the way, like, for example, dietary supplements, or the public good.

Recently pro-industry legislators created an Adverse Event Reporting system for dietary supplements that tries to ignore the role of the many drugs many people use in distorting their metabolism and leading to . Naturally, this created a great PR opportunity to bash and diminish the importance and safety of dietary supplements which do not kill people. Drugs kill people. Foods which are not contaminated do not and dietary supplements are foods!

Dr. Ron Paul, Congressman from Texas, last year called one FDA maneuver an “abuse of power…” and Congress passed dangerous bill under the guidance and force of Senator Ed. Kennedy that further enhanced the power of the FDA. In this case, though, the Health Freedom movement had a partial victory in that we insisted that Congress add a clause to the bill, protecting Dietary Supplements… and Congress, responding to the hundreds of thousands of messages that advocates of health freedom, generated, through our Action Items and otherwise, adopted the protective language.

Yet we recall that genetically modified yeast which produced contaminated Tyrptophane did kill people, giving the FDA the excuse it was seeing to remove this safe and effective sleep and calming amino acid from the market. It was, after all, cutting into the drug market heavily. The FDA did not take genetically modified products off the market. And the company which produced the contaminated shipment in Japan had a sudden and very mysterious fire which destroyed the factory – and any evidence of contamination – almost immediately after the incident was revealed.

Such is the corruption of an agency which regulates both food and drugs. Clearly, those functions must be separated and a new agency which is consumer controlled must be created. Click here () to make sure that happens!

In the meantime, read the important analysis of the latest “Dietary Supplements are Poisonous” disinformation and make a recurring 100% tax deductible donation (https://www.staging.healthfreedomusa.com/index.php?page_id=189) to the Natural Solutions Foundation so that we can continue to provide information and strategic input to keep your health freedom free.

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.Organics4U.org
www.NaturalSolutionsMarketPlace.org
www.NaturalSolutionsMedia.tv

1:12 PM

FOR IMMEDIATE RELEASE
Orthomolecular Medicine News Service, October 9, 2008

(OMNS, October 9, 2008) “Dietary supplements cause 600 ‘adverse events'”, reported USA Today on 22 Sept, 2008. In an article that looks much like an official US Food and Drug Administration press release, it said that “Serious side effects from the use of food supplements resulted in 604 “adverse-event” reports – a list that includes at least five deaths – through the first six months that such accounts have been required by law.” (1)

Good grief! Looks like all those supplement-popping health nuts really are nuts after all. Food supplements simply must be dangerous!

Or are they?

Later on in the article, far from the headline, USA Today conceded that “An adverse event can be anything from a concern that a supplement isn’t working to a serious illness that follows consumption.” And, FDA spokesman Michael Herndon admitted that of the five deaths and 85 hospitalizations reported, “Some of these deaths were likely due to underlying medical conditions.”

FDA’s method of gaining data is suspect at best and biased at worst. Their “Dietary Supplement Adverse Event Reporting” webpage,
http://www.cfsan.fda.gov/~DMS/ds-rept.html, states: “FDA would like to know when a product causes a problem even if you are unsure the product caused the problem or even if you do not visit a doctor or clinic.” The measure of uncertainty involved in publicly soliciting adverse reports “even if you are unsure that the product caused the problem” is noteworthy.

But most significant of all is that FDA refused to disclose exactly which supplements allegedly were causing problems. Doesn’t the public have a right to know? In the absence of FDA disclosure to the contrary, it is likely that the five or fewer deaths attributed to “food supplements” were in fact due to medicinal substances marketed as dietary supplements. FDA acknowledges this in a round-about way at their website
(http://vm.cfsan.fda.gov/~dms/mwgblghb.html).

There you will find an “Important Message” which asks health professionals to “Report Serious Adverse Events Associated with Dietary Supplements Containing GBL, GHB, or BD . . . a group of products sold as dietary supplements for bodybuilding, weight loss and sleep inducement which have been determined to pose a significant public health hazard. These products are chemically related ! to gamma butyrolactone (GBL), gamma hydroxybutyric acid (GHB), and 1,4 butanediol (BD), and can cause dangerously low respiratory rates (intubation may be required), unconciousness/coma, vomiting, seizures, bradycardia and death. GBL, GHB and BD have been linked to at least 122 serious illnesses reported to FDA, including three deaths.”

But these substances are not foods. They are not vitamins, and they are not minerals, and they are not amino acids. They should not be considered with or as food supplements. Over half of all Americans safely take nutritional supplements every day. If each of those persons took only one tablet per day, that would be some 145,000,000 individual doses daily, for a total of over 53 billion doses annually. Many healthy people take more. And yet, according to national statistics compiled by the authoritative American Association of Poison Control Centers, there is not even one death per year from vitamins. (2) Look at the reports, which detail each individual vitamin, mineral, amino acid and herb, and see for yourself at
http://www.aapcc.org/dnn/NPDS/AnnualReports/tabid/125/Default.aspx

By comparison, FDA acknowledges that prescription drugs resulted in 482,154 adverse-event reports in the year 2007. That is nearly 400 times as many adverse events from prescription drugs per six-month period. And this much higher number does not include over-the-counter drugs, a striking omission. Many non-prescription drugs, such as Tylenol (acetaminophen), are a long way from safe. Liver toxicity from acetaminophen poisoning is by far the most common cause of acute liver failure in the United States. Acetaminophen accounted for 51% of all acute liver failure cases in 2003. (3) Indeed, the Associated Press previously reported that common drug dangers are so bad that “Harmful reactions to some of the most widely used medicines – from insulin to a common antibiotic – sent more than 700,000 Americans to emergency rooms each year.” (4)

Vitamin supplements compete with FDA-sponsored drugs. FDA has been trying to eliminate availability of vitamin supplements for over 45 years. As early as 1962, writes constitutional attorney Jonathan W. Emord, “FDA perceived a competitive threat emerging to drug regulation from the sale of dietary ingredients at above RDA doses.” In 1966, “FDA published a rule that any dietary supplement exceeding 150% of the RDA for a vitamin or mineral would automatically be regulated as a drug.” In 1976, after a “public outcry,” the Proxmire Amendment prohibited FDA from deeming a vitamin or mineral a drug solely because of potency. “Undaunted,” continues Emord, “FDA tried yet again to rid the market of vitamins in the 1970s by claiming on a case by case basis that they were adulterated based on their potency.” FDA also tried to have supplements declared to be unapproved food additives. “FDA’s position was a logical absurdity: Single ingredient dietary supplements were food additives b! ecause the ingredients were added to a gelatin capsule which was, FDA said with a wink and a smirk, a food. . . The United States Court of Appeals for the Seventh Circuit described FDA’s position as an “Alice in Wonderland” approach.” In 1980, FDA tried to get vitamins classified as over-the-counter drugs. . . FDA has repeatedly exceeded the limits of its statutory authority to bring about changes designed to protect drug companies from competition.” (5)

Additional evidence comes directly from FDA, whose own Dietary Task Force Report, released June 15, 1993, said: “The task force considered many issues in its deliberations including to ensure that the existence of dietary supplements on the market does not act as a disincentive for drug development.” There is also this statement was made by FDA Deputy Commissioner for Policy David Adams, at the Drug Information Association Annual Meeting, July 12, 1993: “Pay careful attention to what is happening with dietary supplements in the legislative arena . . . If these efforts are successful, there could be created a class of products to compete with approved drugs. The establishment of a separate regulatory category for supplements could undercut exclusivity rights enjoyed by the holders of approved drug applications.”

FDA wants control of vitamins. Their latest ploy is to frighten the public into thinking vitamin supplements are dangerous, without proof, and without even naming the supplements they accuse. Don’t fall for what Abram Hoffer, M.D., calls “the FDA’s grand lie that, if told over and over again, is accepted as somehow true.”

Vitamin supplements are not the problem. Poor eating habits, and too many medicines, are the problem. Food supplements are a solution. They are effective, and vastly safer than drugs. The US Food and Drug Administration knows this full well.

References:

(1) Perez AJ. Dietary supplements cause 600 ‘adverse events’. USA Today, Sept 22, 2008:
http://www.usatoday.com/news/health/2008-09-22-supplements-adverse-events_N.htm
or http://www.usatoday.com/news/health/2008-09-22-supplements-adverse-events_N.htm?POE=click-refer

(2) Annual Reports of the American Association of Poison Control Centers’ National Poisoning and Exposure Database, 3201 New Mexico Avenue, Ste. 330, Washington, DC 20016. Download any report from 1983-2006 at
http://www.aapcc.org/dnn/NPDS/AnnualReports/tabid/125/Default.aspx
free of charge. The “Vitamin” category is usually near the end of the report. Summary and commentary at:
http://www.doctoryourself.com/vitsafety.html

(3) Larson AM et al Acetaminophen-induced acute liver failure: results from a United States multicenter, prospective study. Hepatology 2005;42:1364-1372. See also:
http://www.medpagetoday.com/Psychiatry/Depression/tb/2233

(4) Associated Press, Oct 17, 2006.
http://www.msnbc.msn.com/id/15305033/

(5) Emord JW. FDA violation of the rule of law. Speech from the Health Freedom Exposition in Richmond, Virginia September 23, 2006.
http://www.emord.com/events/speeches/fda_violation.htm

Nutritional Medicine is Orthomolecular Medicine

Orthomolecular medicine uses safe, effective nutritional therapy to fight illness. For more information:
http://www.orthomolecular.org

The peer-reviewed Orthomolecular Medicine News Service is a non-profit and non-commercial informational resource.

Editorial Review Board:

Damien Downing, M.D.
Harold D. Foster, Ph.D.
Steve Hickey, Ph.D.
Abram Hoffer, M.D., Ph.D.
James A. Jackson, PhD
Bo H. Jonsson, MD, Ph.D
Thomas Levy, M.D., J.D.
Erik Paterson, M.D.
Gert E. Shuitemaker, Ph.D.

Andrew W. Saul, Ph.D., Editor and contact person.
Email: omns@orthomolecular.org
http://alobar.livejournal.com/3062139.html

Mighty Mouse is Here – And You’re IT!

Monday, October 13th, 2008

Here’s the wonderful letter Nick Molorisi wrote to us yesterday. Take a moment to read it, realize that YOU are Mighty Mouse and then take the actions listed at the end of this email!
Thanks!
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.Organics4U.org
www.NaturalSolutionsMarketPlace.org
www.NaturalSolutionsMedia.tv

Hi Everybody Mighty Mouse Is Back!
How many of you remember the days when Mighty Mouse cartoons produced an unusual hero. If you do, you are admitting to getting old!

Mighty mouse is back to champion the quest for our freedoms! Dr. Laibow had brought attention back to this mighty warrior for American Freedom like no other, and brought Mighty Mouse back into play. The Mighty Mouse is in right in your hand when you are sitting at your computer!

The opposition starts their agenda of toxic cocktails in our food and medications in one state, mostly among the poor and out of work people.Then they go for the kill by making it the law of the land through our congressmen and senators, and our local law enforcement officials being brain washed
to think of the people they are supposed to, by their oath to protect and defend, are the enemy.

Yet there is a double standard here. These officials of the law don’t realize they are not above the law and that they are being duped, because eventually the fires of this hell on Earth will engulf their own children [and them – REL]. By then it will be too late for even them to say “no” to the demise of their own children.

If our ELECTED OFFICIALS are allowed to continue to force these vaccination agendas, (the attack of the week), on New Jersey, We the People, will all suffer greatly. Then to complete the job, they follow up with the forced psychiatric drugging of our children [and of us -REL] to produce a nation of prescription drug junkies.

It’s up to every one of us to keep at it [defending our freedoms -REL], just like the opposition does at bringing this country down.

We are Mighty Mouse

All of us must use our computer mouses and keep vigil every day by clicking away at all the petitions, faxes, phone calls and letters to these hypnotized and brain-washed so called representatives of the people. Our Foundation’s mission is to educate decision makers… with your help!

Help New Jersey right now…

[By going to the October 16 No Forced Vaccination Rally in Trenton, NJ (https://www.staging.healthfreedomusa.com/index.php?p=1166) and letting everyone you know in the tri-state metro area know about this opportunity – REL] by clicking away on your mouse no matter what state you are from. Sign these very important petitions. The Internet is our greatest tool right now to bring about the freedoms so badly needed in our nation.

Everybody, please — hand on your mouse right now and sign all of the petitions in this forwarded message, and get them to all your contacts. [Free Speech is a good place to start. Click here, http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=25929, to tell your State and Federal Legislators that allowing Registered Dietitians a monopoly over ALL speech relating to food, food components, including dietary supplements, and health is unconstitutional and must stop. Right now, 46 States have such laws with New Jersey hard on their heels. -REL]

Yesterday (Nov, 17, 2007) it was Maryland, where they forced the toxic vaccination program on poor
unsuspecting people [2300 children were vaccinated, 1100 of them RE-vaccinated with an extra dose of toxins because the school district admitted it had lost their vaccination records -REL] at the point of a gun with police dogs and judge in attendance, with police toting guns and attack dogs, to vaccinate their children under severe, cruel and unusual punishment if they did not. [And this in a State with statutory exemptions of medical conditions, conscience and religion, none of which were identified to parents who were threatened with jail time and fines if they did not allow their children to be vaccinated. -REL]

Make no mistake, this is an attack

The CDC’s own website on adverse vaccine incidents [Vaccine Adverse Event Reporting System, VAERS, http://vaers.hhs.gov/ -REL] reported many adverse events related to these toxic medicines on [our -REL] children, but none of this toxic genocide of our children got reported through the media. They bury it with our children who don’t survive this attack, and we get the bill for the whole thing. Your children will be next if we do not act now and help our neighbors. Make no mistake about this. The people of New York State kicked them in the ass by screaming so loud they sent the reps running with their tails between their legs, and got the forced vaccine program squashed in that state.

The opposition is on the attack again.
Today it’s New Jersey. They are escalating the attack on our children of all citizens of this state.

Tomorrow it’s the rest of the country, then in a domino effect, the rest of the world.

Go to your mouse now, and make it Mighty Mouse.

We are talking about maiming and killing your children here. Let’s continue to flood the government offices with our demands that they begin to represent the people or we kick them out this November.

Is it already too late…

These very reps defied the 96% of the people who did not want it in the latest fiasco on the Bail Out, and voted it into law. Where is the serve and protect the people. When you are
broke, who will bail you out? Hmmmmmmm.

They just took your money and will continue to do it if we don’t stop them. It is only the beginning.

This is how we can stop this horror cold.

Remember the kick in the ass will be when, We the People, kick them out of their jobs this November.

Might Mouse is right here, It’s YOU, and we are all a part of this brave warrior for freedom.

Sign the petitions here Natural Solutions Foundation message. [links which follow this message. Then forward it to everyone you know with your own cover message asking people to do the same. Tell them it’s important to you and you believe it will be important to them, too- REL].

Join in and sign up for the free Health Freedom eAlert e-mail messages here: https://www.staging.healthfreedomusa.com/index.php?page_id=187

It only takes a few minutes of your time. And above all, sign or not, get this to all your contacts.

Remember, third party all the way will save the day. No one is going to do this for you, you must get involved. You have to be in it to win it. Do your part and feel proud. Use your mouse to find who your state and national third party reps are, and make it a mighty mouse. Vote for them in November.

Don’t believe for a New York minute that we can’t win. We can!

The only thing you have to fear is what will happen to you and your family if you do nothing.
If you are not part of the solution, you are part of the problem.
Thanks,
Nick Merolesi

Now it’s up to you, Mighty Mouse! Here are the steps to take right now! There isn’t a New York Minute to waste!

* Urge your legislator to become a co-sponsor of Denis Kucinich’s 3 bill suite to demand safety evaluation and labeling of all GMO foods, including the newly approved Franken Meats.
o Click here: http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=25920
* Sign the Tiburon Declaration to let the entire nation know that you are in the majority opposing forced drugging or vaccination. Click here: https://www.staging.healthfreedomusa.com/index.php?p=460
* Keep Codex tyranny over truthful speech about the relationship about the relationship between food and health out of the US.
o Click here: http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=25929
o and Here: http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=26028
o and Here: http://salsa.democracyinaction.org/o/568/t/1134/campaign.jsp?campaign_KEY=1035
* Let your State and Federal Legislators know that you want mercury out of our mouths and out of all health care – NOW!
o Click here: http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=26052

No Forced Vaccination Rally – Trenton, NJ – Oct. 16, 2008

Monday, October 13th, 2008

UPDATE: Rally a Huge Success!

See: http://vitaminlawyerhealthfreedom.blogspot.com/2008/10/no-forced-vaccination-rally.html

Tell your State Representatives that you want strong exemptions from mandatory vaccination (Action Item works for you no matter which State you live in):

http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=21833

————–
This is the latest announcement about this Thursday’s Pro Health Freedom Rally in Trenton. Please forward this information to anyone in the region who can get to this important show of solid support for health freedom.

One Thousand People Expected To Rally For Vaccination Choice
at the State House in Trenton, NJ on Thursday, October 16, 2008 at 12:00 p.m.

NJ Assemblywoman Charlotte Vandervalk, Board-certified Pediatrician Dr. Lawrence Palevsky and National Vaccine Information Center co-founder Barbara Loe Fisher, will join NJ parents and professionals at a rally in Trenton for vaccination choice. Nearly one thousand people are expected, requiring Trenton to close the streets to accommodate the crowds.

The speakers represent a cross-section of society including medical doctors, nurses, chiropractors, scientists, clergy, educators, soldiers, politicians, journalists, autism activists, homeschoolers and many parents. The NJ Coalition for Vaccination Choice (NJCVC) invites you to rally with them by the steps of the State House, outside Gov. Corzine’s office.

The group opposes the four new vaccine mandates including an annual flu shot for children ages 5 and under, required for daycare and pre-school. NJCVC supports the passage of bill A260/S1071, a conscientious exemption to mandatory immunization which will permit parents to select all, some or no vaccinations for their children. A form of this parental right already exists in 19 other US states. All legislators will be in Trenton for a Special Session. Fox News plans to cover the event. Fox aired a live segment on vaccination choice in NJ on October 9 (see http://tinyurl.com/3nmgqb and http://tinyurl.com/45ca5y).

Press urged to cover this high visual impact event: signs, banners, balloons, photos, children, music, personal stories, legislator appreciation ceremony. Rally Information: Rain or Shine, Thursday, October 16, 2008, Noon- 2 pm, 125 West State Street, Trenton, NJ, www.njvaccinationchoice.org for more rally details.

Contact Louise Habakus vaxRSVP@verizon.net 917-553-4634.

Max will be speaking at the Rally. Natural Solutions Foundation Trustee Ralph Fucetola, representing the largest health freedom organization in the world, The Natural Solutions Foundation, will be speaking at the rally.

Max’s Storyhttp://www.youtube.com/watch?v=YswnGsfZsQI
Here is our anticipated
–x–x–

Natural Solutions Foundation
www.HealthFreedomUSA.org

Media Release: End All Forced Vaccination

Trenton, October 16, 2008 – Natural Solutions Foundation participates in the Rally for Vaccination Choice at the Statehouse in Trenton, New Jersey today. Through its www.HealthFreedomUsa.org web site, the Foundation is the largest international ‘netroots’ Health Freedom alliance in the world.

Foundation trustee and life-long New Jersey resident Ralph Fucetola JD delivered a special message to the Rally from Foundation President Maj. Gen. Bert Stubblebine (USA, ret) and Medical Director Rima E. Laibow, MD. The message stated,

“Natural Solutions Foundation supports the efforts of people around the world who oppose forced vaccination for any purpose. As an educational, nongovernmental organization we seek to inform legislators and decision makers about the dangers of vaccine induced disease and the necessity of a Universal Right to Vaccine Exemptions, including strong religious, philosophical and medical exemptions for all vaccines. We congratulate New Jersians on their efforts to stop the uninsurable risks of mandated vaccines.”

Counsel Fucetola continued, “The fact that the insurance industry, our society’s experts in risk, will not insure vaccines is a very telling fact. Without the special Federal Vaccine Injury Compensation Program (VICP) tax that every person who is mandated to buy vaccines is forced to pay, there could be no mandated vaccines at all. Public companies cannot invest in uninsurable risks, so Congress, ever supine to the interests of Big Pharma, mandated that the victims have to pay a tax to guarantee pharmaceutical industry vaccine profits. So far, over two billion tax dollars has been paid out to the families of children maimed and killed by vaccines. This must stop now!”

The Natural Solutions Foundation, along with other health freedom advocates, declared, a year ago, that ending forced vaccinations must be a top priority of all freedom activists. The Tiburon Statement, named after the California town where it was written at an emergency meeting of nongovernmental organizations, can be found at: https://www.staging.healthfreedomusa.com/index.php?p=460 – it states:

Convening for Health Freedom of Choice, Protecting our Children from Forced Vaccination
Health and Freedom leaders and advocates, meeting in an emergency strategic session at Tiburon, California and electronically, declare –

– We collectively call upon Congress and State Legislatures to take immediate steps to restore and guarantee freedom of choice in vaccination and health care and to protect our children and us against forced treatments.

– The moral imperative embodied in the World Medical Association Declaration of Helsinki forbids involuntary medical treatment or experimentation in the absence of fully informed, voluntary consent.

– We have a right to legal protection against mandatory inoculations of our children, such as those which occurred on November 17, 2007 in Prince George’s County Court House, enforced by police.

– Taxpayers have paid nearly $2 billion to compensate families for the death or disability of their children due to vaccination.

We, the undersigned, call upon the Congress of the United States and legislators of each State to adopt the strongest possible legal protections to ensure health care freedom of choice, including the universal right to vaccination exemptions.

Further information: Ralph Fucetola JD- ralph.fucetola@usa.net – http://vitaminlawyerhealthfreedom.blogspot.com/