The Natural Solutions Foundation has been deeply concerned for some time now about the possibility, enshrined in Executive Order, Homeland Security Directive, Patriot Actis 1 and HS Declares ‘Health Emergencies’ to Limit Legal Liability for harm done to victims of vaccine injury and other preventable medical disasters. We note with great alarm that the mechanism of “Emergency” declarations is being used with increasing frequency and take this opportunity to share with you a very serious issue which we urge you to take seriously and heed the potentially dire implications of.
Please remember that the Natural Solutions Foundation is the only organization pulling all of these threads together to give you a comprehensive picture of the threats to your health freedom, and our successes in protecting it.
And please give generously to support this organization working hard to keep your health freedom free. Click here (http://drrimatruthreports.com/index.php?page_id=189) to make your tax deductible contribution to health keep freedom free.
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
http://www.legitgov.org/HHS_declares_health_emergencies.html
HHS Declares ‘Health Emergencies’ to Limit Legal Liability for Anti-
terrorism Vaccines, Drugs
By Lori Price
www.legitgov.org
October Surprises: The U.S. Health and Human Services Secretary,
Michael Leavitt, has declared a series of ‘public health emergencies’
— due to risk of a bioterrorism attack — that continue through 2015.
Oct. 1, 2008: U.S. declares a ‘public health emergency’ due to the
risk of a bioterrorism attack. HHS Secretary, Michael Leavitt, said
the emergency began on Oct. 1 and would run through Dec. 31, 2015.
The declaration establishes legal immunity for public and private
officials who oversee the production or distribution of the anthrax
vaccine.
Oct. 10, 2008: U.S. declares more ‘public health emergencies’ for
smallpox, radiation sickness from the detonation of a nuclear device
and poisoning from botulinum toxins, the active ingredient of Botox.
This move provides the manufacturers, distributors, and others, of
‘anti-terrorism’ drugs and vaccines immunity from lawsuits, should
injuries or deaths occur due to the drugs or vaccines.
U.S. Limits Anthrax Vaccine Legal Liability By Elaine M. Grossman 07
Oct 2008 The U.S. Health and Human Services Department early this
month moved to shield government, industry and business officials
from lawsuits filed by those who have received the anthrax vaccine
(see GSN, Sept. 5, 2007). Health and Human Services Secretary Michael
Leavitt established legal immunity for public and private officials
who oversee the production or distribution of the anthrax vaccine by
declaring a “public health emergency†due to the risk of a
bioterrorism attack. He said the emergency began on Oct. 1 and would
run through Dec. 31, 2015. U.S. law provides protection from lawsuits
to individuals responsible for selected countermeasures, including
antibiotics, during a declared emergency. Under the Public Readiness
and Emergency Preparedness Act, which President [sic] George W. Bush
signed into law in December 2005, a health and human services
secretary’s emergency declaration can limit financial risk for
government program planners and the manufacturers or distributors of
pharmaceutical countermeasures.
Emergency declarations smooth way for vaccine makers –Consumer
advocates see action as giveaway to the drug industry that strips the
public of legal protections. 17 Oct 2008 In a little noticed move,
federal officials this month have declared a series of public health
emergencies relating to potential weapons of biological terror. On
Oct. 1, Health and Human Services Secretary Mike Leavitt declared an
anthrax public health emergency. On Oct. 10, he declared health
emergencies for smallpox, radiation sickness from the detonation of a
nuclear device and poisoning from botulinum toxins, the active
ingredient of Botox. There’s no clear evidence that terrorists have
managed to weaponize anthrax or stolen large caches of Botox from
cosmetic surgeons in Beverly Hills. But by declaring these public
health emergencies, HHS has granted manufacturers of anti-terrorism
drugs and vaccines and others involved with the products protection
from lawsuits if the drugs were to cause unfortunate side effects.
Bogus Anthrax ‘State of Emergency’ Protects Drugmakers, Not Public By
Brandon Keim 15 Oct 2008 Not a single case of human anthrax has been
reported in the United States this year, but the nation is now
officially in a state of anthrax emergency. The emergency was
declared earlier this month by the Department of Health and Human
Services, and will last until 2015. Whether it will protect public
health is debatable, but it will certainly protect makers of faulty
anthrax vaccines. Emergency exemption from legal liability is granted
to vaccine manufacturers by the Public Readiness and Preparedness
Act, passed in 2005 to protect against paralyzing lawsuits during
outbreaks of anthrax, avian influenza or other potentially pandemic
diseases. The act is supposed to be invoked when the Secretary of
Homeland Security has determined “that there is a domestic emergency,
or a significant potential for a domestic emergency, involving a
heightened risk of attack with a specified biological, chemical,
radiological, or nuclear agent or agents.”
37 human anthrax cases in northern Iraq outbreak 12 Oct 2008 Thirty-
seven people have been infected by anthrax in northern Iraq in the
country’s first outbreak of the disease since the 1980s, the health
minister in the Kurdish autonomous region said on Sunday. Health
Minister Ziryan Othman said the disease appeared to have been passed
on from livestock [?]. The first human case of the outbreak was
discovered in remote Dahuk province last month.
US controls bird flu vaccines over bioweapon fears 11 Oct 2008 When
Indonesia’s health minister stopped sending bird flu viruses to a
research laboratory in the U.S. for fear Washington could use them to
make biological weapons, Defense Secretary Robert Gates laughed and
called it “the nuttiest thing” he’d ever heard. Yet deep inside an 86-
page supplement to United States export regulations is a single
sentence that bars U.S. exports of vaccines for avian bird flu and
dozens of other viruses to five countries designated “state sponsors
of terrorism.” The reason: Fear that they will be used for biological
warfare.
Mail carriers, escorted by police, to bring drugs in anthrax attack —
HHS science advisor: Attack using crop-dusting airplane dumping
anthrax spores over a city is a possible scenario 01 Oct 2008
Government mail carriers would deliver emergency supplies of
antibiotics to people in U.S. cities in the case of an anthrax
attack, U.S. Department of Health and Human Services officials said
on Wednesday. The system has been tested in three large [blue] cities
— Seattle, Philadelphia and Boston — and a pilot program is set to
begin soon in the Minneapolis-St. Paul area in Minnesota. The U.S.
Postal Service carriers who would bring the antibiotics from door to
door all would be volunteers who would have advance supplies of
antibiotics to protect themselves and their families, officials said.
Following any new attacks, the mail carriers would be escorted by
local police as they deliver supplies of a few days’ worth of
antibiotics directly to residences throughout an affected community,
HHS Secretary Mike Leavitt said.
HHS Announces New Steps in Anthrax Preparedness (dhs.gov) 01 Oct 2008
HHS Secretary Mike Leavitt today announced two new actions in the
department’s ongoing activities to bolster the nation’s preparedness
for a potential outdoor anthrax attack. In development since March of
this year, the steps being implemented today build upon more than a
decade of preparedness efforts across HHS and other agencies of the
federal government. The first of today’s actions focuses on United
States Postal Service letter carriers who volunteer to deliver
medicines directly to residences in their communities during an
emergency… Over the past several years, under the Cities Readiness
Initiative (CRI), HHS and the Postal Service have successfully
developed and tested in three U.S. cities — Seattle, Philadelphia
and Boston –the ability of letter carriers to quickly deliver door-
to-door quantities of antibiotics from the Strategic National
Stockpile to residential addresses. This quick-strike capability is
intended to buy time for local and State public health authorities to
set up points of dispensing for further provision of antibiotics
across the community.
Judge Affirms Win for Plaintiffs in ‘Anthrax I’ Case By Elaine M.
Grossman 05 Sep 2007 For the first time, a federal judge last month
declared six U.S. defense personnel the definitive winners in a four-
year court battle over the anthrax vaccine. The Aug. 21 decision,
which revolves around payment of attorneys’ fees, is the latest
chapter in a protracted struggle over whether the Defense Department
can require service members to take the anthrax vaccine. U.S.
District Court Judge Emmet Sullivan decided the government defendants
must pay the plaintiffs’ expenses because the plaintiffs won the
case. The litigants — defense personnel who were required to take
anthrax vaccine shots in a Defense Department effort that began in
1998 — won the first round of litigation in October 2004, when
Sullivan issued a permanent injunction banning mandatory
inoculations. Based on a finding that the vaccine was never certified
to protect against “weaponized” airborne anthrax spores, the judge
declared the Pentagon’s mandatory vaccinations “illegal.”
HOMELAND SECURITY PRESIDENTIAL DIRECTIVE/HSPD-21, issued 18 October
2007, states that within one year of the directive’s date, ‘the
Secretaries of Health and Human Services and Defense, in coordination
with the Secretaries of Veterans Affairs and Homeland Security, shall
establish an academic Joint Program for Disaster Medicine and Public
Health housed at a National Center for Disaster Medicine and Public
Health at the Uniformed Services University of the Health Sciences…
Department of Health and Human Services and Department of Defense
authorities will be used to carry out respective civilian and
military missions within this joint program.’
Dr. Mae Won Ho is a brilliant and fearless truth teller. Her science is impeccable and her voice is loud and strong when it comes to telling the truth about dangerous make believe science. Nowhere is she more vigorous in alerting us to the absurdities and deadly consequences of corporate junk science and junk policies than in the area of Genetically Modified Organisms or GMOs.
The following article is a must read, must share one which I urge you to forward to as many people as possible so that they can join forces to make sure that all legislators understand that the FDA and USDA are not protecting our interests and Congress must take the reins from them before their criminal negligence kills us all.
The reallity is that stark.
Click here (http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=25920) to urge your legislators to become supporters of the suite of bills introduced by Rep. Denis Kucinich to require safety assessments of GMOs and require clear labeling of all GMO ingredients and components of food.
And then click here (http://drrimatruthreports.com/index.php?page_id=189) to make a tax deductible, recurring donation so that the Natural Solutions Foundation can continue to bring you the facts you need about your health freedom.
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
GM is Dangerous and Futile
We Need Organic Sustainable Food and Energy Systems Now
New genetics research invalidates the science underpinning the $73.5 billon global biotech industry and confirms why genetic modification is futile and dangerous; we must implement organic sustainable food and energy systems now Dr. Mae-Wan Ho
Invited Lecture at Conference on Future of Food: Climate Change, GMOs and Food Security, 1-2 October 2008, India International Centre, New Delhi
A fully referenced version of this article is posted on ISIS members’ website. Details here
An electronic version of this report with full references can be downloaded from the ISIS online store. Download Now
digg Add to My Yahoo!
I am deeply and doubly honoured to be part of this important conference on Mahatma Gandhi’s birthday, because it was Vandana Shiva and Tewolde Berhan Gebre Egziabher who inspired me and turned me from an ivory tower academic into a science activist. Consequently, I was thrown out of my university and liberated to join civil society in fighting corrupt science and protecting good independent science.
Food Futures Now , *Organic *Sustainable *Fossil Fuel Free, How organic agriculture and localised food, and energy systems can potentially compensate for all greenhouse gas emissions due to human activities and free us from fossil fuels “Change to gene theory raises new challenges for biotechâ€
The headline appeared in the business section of the International Herald Tribune 3 July 2007 [1]. The article went on to say: “The $73.5 billion global biotech business may soon have to grapple with a discovery that calls into question the scientific principles on which it was founded.â€
It was referring to the findings of project ENCODE (Encyclopedia of DNA elements), organised by the US National Human Genome Research Institute. A consortium of 35 research groups went through 1 percent of the human genome with a fine-tooth comb to find out exactly how genes work.
To their surprise, researchers found that the human genome might not be a “tidy collection of independent genes†after all…Instead, genes appear to operate in a complex network, and interact and overlap with one another and with other components in ways not yet fully understood.â€
The Human Genome Research Institute said that these findings will challenge scientists “to rethink some long-held views about what genes are and what they do.â€
The author of the article Denis Caruso commented that, “the report is likely to have repercussions far beyond the laboratory. The presumption that genes operate independently has been institutionalized since 1976, when the first biotech company was founded. In fact, it is the economic and regulatory foundation on which the entire biotechnology industry is built.†She went on to point out that gene patents and safety assessment based on the same paradigm are also in trouble.
She is right on all counts. I pointed that out 10 years previously when a plethora of findings in molecular genetics had already invalidated the genetic determinist paradigm underpinning the biotech industry. In fact, the paradigm had begun to unravel almost as the industry was starting up twenty years earlier.
The Brave New World of GM Science
In Genetic Engineering Dream or Nightmare, the Brave New World of Bad Science and Big Business [2] first published in 1997/1998 I explained why the science behind GM is wrong and obsolete, and hence dangerous; a story elaborated further in Living with the Fluid Genome [3] published in 2003.
Genetic engineering of plants and animals began in the mid 1970s in the belief that the genome (the totality of all the genetic material of a species) is constant and static, and that the characteristics of organism are simply hardwired in their genome. This was encapsulated in the Central Dogma of molecular biology. The genetic information goes from DNA, the genetic material, to RNA, a kind of intermediate, to protein which determines the characteristic involved, such as tolerance to herbicide, for example. One gene determines one trait, so you can transfer one gene and get exactly the trait you want, be it herbicide tolerance, or resistance to insect pest.
But geneticists soon discovered that the genome is remarkably dynamic and ‘fluid’. It is constantly in conversation with the environment, and that determines which genes are turned on, when, where, by how much and for how long. Moreover, the genetic material itself could also be marked or changed according to experience, and the influence passed on to the next generation. Most of that was known by 1980, long before the Human Genome Project was conceived.
The best thing about the Human Genome Project is to finally explode the myth of genetic determinism [4] (The Myth that Launched a Thousand Companies, SiS 18), revealing the layers of molecular complexity that transmit, interpret and rewrite the genetic texts [5] (Life Beyond the Central Dogma series, SiS 24). The ENCODE project has confirmed and extended the complexities especially with regard to what constitutes a gene. Traditionally, a gene is a sequence of DNA that codes for a protein with a well-defined function. This idea has been well and truly shattered [6]; as Barry Patrick wrote in the Science News [7] “genes are proving to be fragmented, intertwined with other genes, and scattered across the whole genome.â€
The genetic engineer’s idea of a gene is presented in Figure 1. It has a regulatory signal, a promoter that says to the cell, go and make lots of copies of the coding sequence that would be translated into a protein, and a terminator that says stop, end of message. This is what genetic engineers put into cells to make a genetically modified organism (GMO).
A gene expression cassette, the genetic engineer’s idea of a gene
Figure 1. A gene expression cassette, the genetic engineer’s idea of a gene
Instead, within the human genome, and indeed other mammalian genomes, coding sequences are in bits (exons) separated by non-coding introns, and exons contributing to a single protein could be in different parts of the genome. Coding sequences of different proteins frequently overlap. Regulatory signals are similarly scattered upstream, downstream, within the coding sequence or in some other distant part of the genome. Coding sequences occupy just 1.5 percent of the human genome, but between 74 and 93 percent of the genome produce RNA transcripts [7], many now known to have regulatory functions. So much so that the project of mapping genetic predisposition to diseases, the original rationale for the Human Genome Project, has now run into serious trouble.
David M. Altshuler, associate professor of genetics and medicine at Harvard Medical School and his research team showed that the risk for type 2 diabetes involves more than a mutated gene. Instead, diabetes, heart disease, some cancers, and other deadly ailments involve non-coding DNA as well as in genes [8]. “We’re realizing that things happening ‘somewhere else’ in the genome, not in genes, are playing critical roles†in sickness and in health, Altshuler said.
David B. Goldstein at Duke University is very pessimistic. He said the effort to nail down the genetics of most common diseases is not working [9]: “There is absolutely no question that for the whole hope of personalized medicine, the news has been just as bleak as it could be. After doing comprehensive studies for common diseases, we can explain only a few percent of the genetic components of most of these traits.†For schizophrenia and biopolar disorder, there is almost nothing, for type 2 diabetes, 20 variants, but they explain only up to 3 percent of familial clustering, and so on.
Goldstein added: “we have cracked open the human genome and can look at the entire complement of common genetic variants, and what do we find? Almost nothing. That is absolutely beyond belief.â€
That is just what I predicted soon after the human genome sequence was announced [10, 11] (Human DNA ‘BioBank’ Worthless, SiS 13/14; Why Genomics Won’t Deliver, SiS 26)
Fresh attempts are now made to redefine a gene either in terms of a protein product [12] or a transcript [13], neither of which are satisfactory or would save the industry. All patents on genes based on the old concept are no longer valid; ultimately because the patent is awarded on a supposed function attached to a DNA sequence. But as genes exist in bits interweaving with other genes, so are functions. Multiple DNA sequences may serve the same function, and conversely the same DNA sequence can have different functions. Again, I have explained Why Biotech Patents Are Patently Absurd [14].
Despite the bewildering complexities of how the genome works, individual processes are precisely orchestrated and finely tuned by the organism as a whole, in a highly coordinated molecular ‘dance of life’ that’s necessary for survival.
In contrast, genetic engineering in the laboratory is crude, imprecise and invasive. The rogue genes inserted into a genome to make a GMO could land anywhere; typically in a rearranged or defective form, scrambling and mutating the host genome, and tend to move or rearrange further once inserted. Transgene instability is a big problem, and has been so right from the beginning. There is fresh evidence that GM crops grown commercially for years have rearranged [15, 16] (MON810 Genome Rearranged Again. Transgenic Lines Unstable hence Illegal and Ineligible for Protection, SiS 38). This is a real opportunity to challenge the validity of all biotech patents. Another key issue is safety. Transgene instability means that the original transgenic line has turned into something else, and even if it had been assessed as ‘safe’, this is no longer the case.
The genetically modified genes are a big hazard because they do not know the intricate dance of life that has been perfected in billions of years of evolution. That’s ultimately why genetic modification is both dangerous and futile.
Thirty years of GM are more than enough
We’d had 30 years of GM and more than enough damage done, as detailed in the ISP Report The Case for A GM-Free Sustainable World [17] and the dossier GM Science Expose : Hazards Ignored, Fraud, Regulatory Sham, Violation of Farmers Rights [18] we compiled for the European Parliament in June 2007. And more evidence has been piling up since. Why has this been allowed to go on? W documented how national and international regulators and advisory bodies such as the European Food Safety Authority not only routinely ignore the precautionary principle, but also actively abuse science, sidestep the law, and helping to promote GM technology in the face of evidence piling up against the safety of GM food and feed [19] (GM Food Nightmare Unfolding in the Regulatory Sham, ISIS scientific publication).
Let me summarize the evidence stacked up against GMOs.
* No increase in yields
Successive reports [17, 18, 20] confirm that the yields of all major GM crops varieties cultivated are lower than, or at best, equal to yields from non-GM varieties. Studies from 1999 to 2007 consistently show that GM soya decreased yields by 4 to 12 percent compared to non-GM soya, while Bt maize yields from 0 to 12 percent less than conventional isolines. Up to 100 percent failures of Bt cotton crops have been recorded in India [18] (and amply confirmed by the farmer witnesses who are here today). New research from the University of Kansas found a 10 percent average yield drag for Roundup Ready soya [21], and extra manganese is needed for the soil Scientists from the USDA and the University of Georgia found growing GM cotton in the US could result in a drop in income by up to 40 percent [22, 23] (Transgenic Cotton Offers No Advantage, SiS 38)
* No reduction in pesticides use
USDA data showed that GM crops increase pesticide use by 50 million pounds from 1996 to 2003 in the United States [17]. New data paint an even grimmer picture: the use of glyphosate on major crops went up more than 15-fold between 1994 and 2005, along with increases in other herbicides [24] in order to cope with rising glyphosate resistant superweeds [6]. Palmer 3pigweed is a major concern in Georgia, with farmer there having to mow cotton down in fields with glyphosate-resistant Palmer amaranth [25]. And following close on the health of that is glyphosate resistant giant ragweed [26]. Roundup tolerant canola volunteers are top among the worries of Canadian farmers [27, 28] (Study Based on Farmers’ Experience Exposes Risks of GM Crops, SiS 38)
* Roundup lethal to frogs and toxic to human placental and embryonic cells [18].
Roundup is more toxic than glyphosate, and it is used in more than 80 percent of all GM crops planted in the world.
* GM crops harm wildlife
UK’s farm scale evaluations have found that GM crops harm wildlife [18]; more recently a study led by Loyola University, Chicago, Illinois in the United Stated, found that wastes from Bt corn impaired the growth of a common aquatic insect [29, 30] (Bt Crops Threaten Aquatic Ecosystems, SiS 36). This is just the tip of the iceberg. There is evidence that GM crops, especially Bt crops contribute to the demise of the honeybee worldwide because it compromises their immune system and make them exra-susceptible to attacks by parasitic fungus (31) (Parasitic Fungi and Pesticides Act Synergistically to Kill Honeybees? SiS 35).
* Bt resistance pests and Roundup tolerant superweeds render the two major GM crop traits practically useless [18].
A recent review concluded that [32] “evolved glyphosate-resistant weeds are a major risk for the continued success of glyphosate and transgenic glyphosate-resistant crops.†And the evolution of Bt resistant bollworms worldwide have now been confirmed and documented in more than a dozen fields in Mississippi and Arkansas between 2003 and 2006 [33]. Worse yet, secondary pests now plague the fields and spread to other crops in India [34] (Deadly gift from Monsanto to India, SiS 38).
* Vast areas of forests, pampas and cerrados lost to GM soya in Latin America
Argentina alone has lot 15 m hectares [18]; and this has worsened considerably with the demand for biofuels (see later)
* Epidemic of suicides in the cotton belt of India
An estimated 100 000 farmers have killed themselves between 1993-2003, and a further 16 000 farmers a year have died since Bt cotton was introduced [18]
* GM food and feed linked to deaths and sicknesses
Evidence of serious health impacts in lab tests and from farmers’ fields around the world (more below)
GM food and feed inherently hazardous to health [19]
Here are some highlights from our GM Science dossier [18] on the hazards of GM food and feed. Dr. Irina Ermakova of the Russian Academy of Sciences showed how GM soya made female rats give birth to severely stunted and abnormal litters, with more than half dying in three weeks, and those remaining are sterile. Hundreds of villagers and cotton handlers in India suffer allergy-like symptoms, thousands of sheep died after grazing on the Bt cotton residues, goat and cows as well were reported in 2007 and 2008 [35] (Mass Protests against GM Crops in India , SiS 38). (As reported by farmer witnesses as this conference, the problem is continuing and sterility in offspring of exposed animals has also been observed.) A harmless bean protein transferred to pea when tested on mice cause severe inflammation in the lungs and provoked generalised food sensitivities. Dozens of villagers in the south of the Philippines fell ill when neighbouring GM maize fields came into flower in 2003, at least five have died and some remain ill to this day. A dozen cows died having eaten GM maize in Hesse Germany and more in the herd had to be slaughtered from mysterious illnesses. Arpad Pusztai and his colleagues in the UK found GM potatoes with snowdrop lectin damaged every organ system of young rats; the stomach lining grew twice as thick as controls. Chickens fed GM maize Chardon LL were twice as likely to die as controls. And finally, GM maize Mon 863 was claimed to be as safe as non-GM maize by the company, and accepted as such by European Food Safety Authority. But independent scientists of CriiGen in France re-analysed the data and found signs of liver and kidney toxicity.
Different animals and human beings exposed to a variety of transgenic crops with different traits either fall ill or die. The evidence compels us to consider the possibility that the hazards of GMOs may be inherent to the technology, as I suggested more than ten years ago [2].
Table 1. Summary of Exposure of Animals and Human Beings to GMOs
Species GM species Transgene trait Effect
Rat Soya Roundup Ready Stunting, death, sterility
Humans Cotton Cry1Ac/Cry1Ab Allergy symptoms
Sheep “ “ Death, liver toxicity
Cows “ “ “
Goats “ “ “
Mice Pea Alpha-amylase Inhibitor Lung Inflammation, General food sensitivity
Mice Soya Roundup Ready Liver, pancreas and testis Affected
Humans Maize Cry1Ab Illnesses and death
Rats Maize Cry3Bb liver and kidney toxicity
Cows Maize Cry1Ab/Cry1Ac Death and illnesses
Rats Potato Snowdrop lectin Damage in every organ system. Stomach lining twice as thick as controls
Mice Potato Cry1A Gut lining thickened
Rats Tomato Delay ripening Holes in the stomach
Chickens Maize Glufosinate tolerance Deaths
An epidemic of Morgellons Disease has hit the US and other countries that had been involved in genetic modification technology [36] (Agrobacterium & Morgellons Disease, A GM Connection?. SiS 38). The pathogen is suspected to be Agrobacterium, which has been widely used in smuggling genes into cells to make GMOs. Is this a disease created by GM? There have been close calls before.
US courts rule GM crop field-tests and releases illegal
The message that GM crops are unsafe appears to have got through to the judiciary system in the United States. There have been three court rulings against the US Department of Agriculture (USDA) for failing to carry out proper environmental impact assessment, making the original releases illegal [37] (Approval of GM Crops Illegal, US Federal Courts Rule, SiS 34). These are the first rulings against GMOs in the top producing country in the world, which has been also promoting GMOs aggressively.
The first case was on drug-producing GM crops in Hawaii. The court said that the USDA violated the Endangered Species Act as well as the National Environmental Policy Act.
The second court case not only ruled GM herbicide-tolerant creeping bentgrass illegal, but also that the USDA must halt approval of all new field trials until more rigorous environmental reviews are conducted.
The third decision was passed on Monsanto’s Roundup Ready alfalfa for having been commercial released illegally without an Environment Impact Statement.
An avalanche of bans and rulings strikes GM crops worldwide
There have been numerous bans and restrictions imposed on GM crops in recent years, which say a lot about the inadequacies of regulatory regimes worldwide (see Box 1).
Box 1
Rulings and bans on GMOs between May 2007 and May 2008
* US GM alfalfa ban made permanent [38]
* US Federal Court of Appeals ruled against GM bentgrass again [39]
* Four counties in California have bans or moratorium on GM crops and the first state bill to protect Californian farmers against lawsuits that intimate and harass them when their field are contaminated passed through the Agriculture committee in January 2008 [40]
* Montville USA became the first town outside California to ban GM crops [41]
* South Australia extended its GM ban [42]
* Romania joined EU members in banning GM crop Mon 810 [43], the others are France, Hungary, Italy, Austria, Greece, and Poland
* 13 out of 20 counties in Croatia have declared themselves GM-Free [44]
* Greece renewed its ban on GM maize seeds [44]
* Germany imposed much stricter regulations on GM maize [46]
* Scotland backs GM ban in Europe [47]
* France banned GM maize Mon 810 in February 2008 and passed GMO law in April to guard against contamination by GMO, making it compulsory for farmers to “respect agricultural structures, local ecosystems and non-GMO commercial and production industries†[48, 49]
* Wales is set to ban GM crops [50]
* Switzerland bans crops until 2012 [51]
* More than 230 regions, over 4 000 municipalities and other local entities and tens of thousands of farmers and food producers in Europe have declared themselves GMO-free so far [52]
EU Commissioner for the Environment Stavros Dimas has expressed serious reservations concerning GMOs [53] (GM-Free Europe Beginning?, SiS 36), which is unprecedented in the history of the European Commission. On 7 May 2008, the European Commission delayed a decision on allowing farmers to grow more GM crops, and asked European Food Safety Authority to reconsider its previous review, which it had admitted was inadequate, as it was unable to take indirect and long term impacts into account [54].
No case for GM crops, small scale organic farming is the way ahead
Meanwhile, on 15 April 2008, 400 scientists of the International Assessment of Agricultural Science and Technology for Development (IAASTD) released its 2 500-page report [55, 56] (GM-Free Organic Agriculture to Feed the Worldâ€, SiS 38) that took 4 years to complete. It is a thorough examination of global agriculture on a scale comparable to the Intergovernment Panel on Climate Change.
The IAASTD calls for a fundamental change in farming practice to counteract soaring food prices, hunger, poverty and environmental disasters, it says GM crops are controversial with respect to safety for health and the environment, and will not play a substantial role in addressing climate change, loss of biodiversity, hunger and poverty. Small scale farmers and agro-ecological methods are the way forward, and indigenous and local knowledge are as important as formal scientific knowledge. It warns that growing crops for biofuels could worsen food shortages and price rises.
The conclusions of the IAASTD are remarkably similar to our own report Food Futures Now *Organic *Sustainable *Fossil Fuel Free [57] launched in UK Parliament a week later.
Our Food Futures Now report goes a step further. We argue that only organic agriculture can truly feed the world. More than that, organic agriculture and localised food and energy systems can potentially compensate for all greenhouse emissions due to human activities and free us from fossil fuels, and we need to implement this urgently.
The UN has declared 2008 the year of the Global Food Crisis, and it has been the top news story everyday for months now as the crisis deepens. Food prices increased by an average of 40 percent last year; a string of food riots and protests spread around the world including the UK, and more than 25 000 farmers killed themselves in India.
Most commentators agree that the immediate cause of the food crisis is the divestment of food grains into producing biofuels. BusinessWeek identified Monsanto as a “prime beneficiaryâ€. Its stock correlated closely with the price of oil (better than ExxonMobile), and hardly correlated with the price of corn, basically because no one will eat its GM corn. Nevertheless the pro-GM lobby are out in force, using the food crisis to promote GM crops.
GM crops are one big failed experiment based on an obsolete scientific theory, and this failure has been evident since 2004 if not before [58] (Puncturing the GM Myths, SiS 22). Apart from yielding less and requiring more pesticides, anecdotal evidence since 2005 from farmers around the world indicates that GM crops also require more water [59]. Industrial Green Revolution agriculture is now generally acknowledged to be a major driver of climate change as well as being vulnerable to climate change because of its heavy dependence on fossil energies and water, and its susceptibility to pests, diseases and climate extremes [56, 60, 61] (Beware the New “Doubly Green Revolution”, SiS 37)..GM crops have all the worst features of industrial Green Revolution varieties exaggerated, and not least, there are outstanding safety concerns as I mentioned. Growing GM crops for biofuels does not make them safe, as they will contaminate our food crops all the same.
Any further indulgence in GMOs will surely damage our chances of surviving global warming. We must get on with the urgent business of building organic, sustainable food and energy systems right now.
printer friendly version
Recent Publications
The Rainbow and the Worm, The Physics of Organisms
The Rainbow and the Worm, The Physics of Organisms “Probably the Most Important Book for the Coming Scientific Revolution†Now in its Third Edition
Buy Now|More info
Food Futures Now
Food Futures Now: *Organic *Sustainable *Fossil Fuel Free How organic agriculture and localised food (and energy) systems can potentially compensate for all greenhouse gas emissions due to human activities and free us from fossil fuels
Buy Now|More info
Science in Society magazine The only radical science magazine on earth
Science in Society 39 OUT NOW! Order your copy from our online store.
GM Science Exposed
GM Science Exposed. A comprehensive dossier containing more than 160 fully referenced articles from the Science in Society archives.
Buy Now|More info
GMO Free: Exposing the Hazards of Biotechnology to Ensure the Integrity of our Food SupplyGMO Free: Exposing the Hazards of Biotechnology to Ensure the Integrity of our Food Supply
Buy Now|More info
Join the I-SIS mailing list; enter your email address html asci
I-SIS is a not-for-profit organisation, depending on donations, membership fees, subscriptions, and merchandise sales to continue its work. Find out more about membership here
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 (http://drrimatruthreports.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
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 (http://drrimatruthreports.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: http://drrimatruthreports.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: http://drrimatruthreports.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
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.â€
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!â€
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: http://drrimatruthreports.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/