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June 25, 2010
URGENT KIWANIS ALERT! IF YOU ARE A MEMBER OF THE KIWANIS SERVICE ORGANIZATION, http://sites.kiwanis.org/kiwanis/en/home.aspx, YOU MUST TAKE ACTION TO STOP YOUR ORGANIZATION FROM COLLABORATING WITH UNICEF IN “PREVENTING MATERNAL AND INFANT TETANUS”. THIS VACCINE IS THE ONE PIONEERED AND USED AROUND THE WORLD BY WHO TO CREATE PERMANENT INFERTILITY IN WOMEN AND GIRLS. PLEASE CONTACT THE KIWANIS ORGANIZATION AND ALERT THEM TO THIS USE OF VACCINATION. DEMAND THAT THEY SET UP CONTROLS TO MAKE SURE THAT THESE ARE NOT DEPOPULATION VACCINATIONS IF THEY ARE DETERMINED TO AID AND ABET A DANGEROUS ACTIVITY USED TO WEAKEN THE IMMUNE SYSTEM.
http://www.medicalnewstoday.com/articles/192937.php
Note: the Vaccine Adverse Event Reporting System, VAERS, reports 333451 adverse events associated with vaccines. This number is generally acknowledged to represent between 1 and 10% of all adverse events. ttp://www.medalerts.org/vaersdb/findfield.php
See also:
http://www.akha.org/content/medicaldocuments/tetanustoxoidcanadalabs.html
http://www.generationcedar.com/main/2009/07/population-control-through-tetanus-vaccine.html
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Find out about this week’s (and future) guests, check out the archives, at http://drrimatruthreports.com/?p=4850
Consider:
POLIO VICTIMS, SIERRA LEONE
CROWD AWAITING POLIO VACCINATION
Stanley Kops….has produced proof positive that the oral polio vaccine has always been contaminated with SV-40, a monkey virus which has been linked by the FDA and other organizations with cancers such as mesothelioma and meduloblastoma. Since 1963, we have been assured that polio vaccines have not contained this deadly contaminant. Stanley Kops shows that not only is this not the case, but that the vaccine regulators who are charged with keeping our families safe, have known all along that SV-40 was never removed from vaccines.
http://www.whale.to/a/sv40a.html
From the CDC: “Inevitable gaps in [Polio] vaccination coverage will give rise to cVDPVs [that is, polio cases caused by the vaccine itself – REL] as long as OPV [Oral Polio Vaccine] use continues”
http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5540a3.htm
Polio outbreaks continue to be associated with circulating vaccine-derived polioviruses (cVDPVs) in areas with low oral poliovirus vaccine (OPV) coverage [Emphasis added-REL]. In addition, long-term excretion of neurovirulent immunodeficiency-associated vaccine-derived polioviruses (iVDPVs) can lead to poliovirus spread to contacts. Overcoming these obstacles is challenging. High rates of OPV coverage will prevent all poliovirus spread, including spread of VDPVs, but will not prevent establishment of prolonged VDPV infections in certain persons with B-cell immunodeficiencies (i.e., having defects in antibody production). Inevitable gaps in vaccination coverage will give rise to cVDPVs as long as OPV use continues.
and then consider that Elswood and Stricker, avid proponents of vaccination, presented evidence in 1994 that HIV was disseminated in polio vaccination by WHO in Africa. This evidence has never been refuted.
http://www.uow.edu.au/~bmartin/dissent/documents/AIDS/Elswood94.html
First, Blame the Victims!
If you read the article below, from the respected Science Daily, you will note that the vaccine establishment acknowledges that the cause of polio is, in many cases, the virus in the vaccine which was supposed to be so attenuated that it could not cause any disease. But the real reason, they assert, is that the people who get polio from the vaccines (mostly children under 5 years of age.
Health Freedom Needs Your Activism AND Your Donations!
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Polio is the classic case of “Problem, Solutions, Reaction” favored by those who drive systems, in this case, our nations and our freedom, into chaos to control and destroy them. Take an environmental toxicity which co-factors with a virus, create a vaccine which spreads the disease, vaccinate widely, cause ‘epidemics’ of small numbers of cases, scare the wits out of parents and community decision makers with false information, deny for decades that the vaccine CAUSES the disease it is supposed to prevent and then, when the market is flagging because it is clear that the vaccination program has not worked, BLAME THE VACCINE FOR SPREADING THE DISEASE IN PEOPLE WITH VULNERABLE IMMUNE SYSTEMS AND THEN CONVINCE PEOPLE, ESPECIALLY DOCTORS, WHO ARE, IN FACT, THE MOST GULLIBLE OF PEOPLE, THAT THE CURE FOR VACCINE-DISSEMINATED POLIO IS TO VACCINATE MORE PEOPLE, ESPECIALLY KIDS!
Oh, wait! While you are doing that, make sure that the vaccine that spreads polio, in this case, ALSO causes another, deferred, more serious disease, in this case ACUTE LYMPHOCYTIC LEUKEMIA! And perhaps just a bit of HIV thrown in for good measure? Sure. People with HIV, in addition to dying, also get lots and lots of cancer!
THE HOUSE THAT CANCER BUILT
Cancer is the most wildly financially productive disease ever encountered by humans. The 2008 cost of cancer in the US, according to the American Cancer Society, funded by Big Pharma itself, was a walloping $228.1 Billion. How many of those dollars were expended on children with vaccine induced cancer? And what is the non-fiscal cost of a child’s life? I do not know how to do that mathematical computation. And the vaccine industry does not care to do it.
Please visit http://drrimatruthreports.com/?p=5706 to learn more about how this works. Then please come back to this article, keep reading and take action!
Polio vaccination is as great a scam as any other vaccination: there is no scientific evidence -none!- that vaccines work to prevent, mitigate or cure any disease. There is vast evidence that they work to weaken the nervous systems and that they intentionally, yes, intentionally, spread diseases which are vast profit sources and shorten lives and eliminate fertility.
We know, from the personal admission of Maurice Hilleman, PhD, or Merck Pharmaceuticals, that the polio vaccine’s leukemia virus contamination has been known for decades while the vaccine was administered to children around the world. I know of nothing to suggest that current polio AND OTHER vaccines are not contaminated with deadly viruses in addition to seriously toxic constituents like mercury and aluminum, Tween 80, human DNA, animal DNA, viruses, formaldehyde, etc. In fact, there is a great deal to document that they are. http://www.thinktwice.com/multiple.htm
And there is also a good deal to document that it is vaccination itself, not just polio vaccination, that causes diseases for which the vaccine allegedly protects the vaccination victim. [Alexa Traffic Rank for http://drrimatruthreports.com/docs/Syringe_of_death.pdf: 149579] http://drrimatruthreports.com/docs/Syringe_of_death.pdf, etc., etc.! http://drrimatruthreports.com/?p=3198.
So read the article below and then share it with everyone you know. Ask them to take the action steps here and, just in case you have not already taken these steps, once for every member of your family, please take a few moments to do so now. Riding the freedom mouse can save your life and your freedom, all in the same swift, easy action step!
Thanks for your activism.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Valley of the Moon™ Eco Demonstration Project
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Now, your activism. First take action below for every member of your family and then forward this email to your entire contact list, asking that they do the same:
1. Call for Congressional Hearing on Autism and Other Environmental Illness: Autism and other environmentally caused diseases, including asthma, MS, at least 85% of all cancers (and much more in children), emphysema, etc., are preventable. Preventable, that is, if Congress takes the bull by the horns, carries out the studies and hearing and then passes legislation to protect the population. Click here, , to demand exactly those actions from the Congress that We, the People, elected and which works for US, the most potent special interest group in existence, 310,000 strong! http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=3688
2. Stop the Food Fascism Bill, S. 510, which masquerades under the title of the “Food Safety” Bill. It makes food profits safe for the multinationals like Monsanto, and guarantees that your food will be contaminated and controlled by those multinationals, not local farmers, including organic farmers. FDA says we do not have the right to decide what we want to eat. Show them they are wrong!
http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=26714
3. End GMO Contamination of Your Food, Your Body, Your Planet. FDA FORBIDS GMO LABELING so you have no idea how much of your food supply is contaminated. Worse yet, GMOs are contagious! The foreign DNA spreads within and between species and the contamination cannot be reversed by any technique we have now short of burning the contaminated material. NO significant safety testing is carried our, or permitted, by government agencies. Ban GMOs and set up a commission to find out how much damage has been done and develop new ways to fix the problem before there IS no fix!
http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=2049
Thanks for donating and taking the important Action Items above. You are a member of the distribution list for the free, secure and very important Health Freedom Action eAlerts, aren’t you? Quick, sign up here, http://drrimatruthreports.com/ (scroll down, sign up!)
Polio Research Gives New Insight Into Tackling Vaccine-Derived Poliovirus
ScienceDaily (June 24, 2010) — A vaccine-derived strain of poliovirus that has spread in recent years is serious but it can be tackled with an existing vaccine, according to a new study published today in the New England Journal of Medicine.
Vaccine-derived polioviruses can emerge on rare occasions in under-immunized populations, when the attenuated virus contained in a vaccine mutates and recombines with other viruses, to create a circulating vaccine-derived strain.
The researchers behind today’s study say their findings highlight the importance of completing polio eradication. They also say that should wild-type poliovirus be eradicated, routine vaccination with oral polio vaccines will need to cease, in order to prevent further vaccine-derived strains of the virus from emerging.
The study was carried out by researchers from the Medical Research Council Centre for Outbreak Analysis and Modelling at Imperial College London, working with the Government of Nigeria and the World Health Organization (WHO) research teams.
Poliovirus is highly infectious and primarily affects children under five years of age. Around one in 200 of the people infected with polio develop permanent paralysis, which can be fatal.
Polio was virtually wiped out by the early 2000s following a major vaccination drive by the Global Polio Eradication Initiative, but since then the number of cases of paralysis reported has plateaued, remaining roughly constant at between one and two thousand each year from 2003 to 2009, dropping only recently in 2010.
The first reported polio outbreak resulting from a circulating vaccine-derived poliovirus, known as a cVDPV, occurred in Hispaniola in 2000. Prior to today’s study, there was little evidence available about the severity and potential impact of this kind of poliovirus.
Although billions of doses of oral vaccine have been distributed in the last decade, just 14 cVDPV outbreaks have been reported, affecting 15 countries. These outbreaks have usually been limited in size.
For the new study, researchers looked at the largest recorded outbreak of a cVDPV to date, which began to circulate in Nigeria in 2005. The authors examined data from 278 children paralyzed by this cVDPV, and compared them with children paralysed by wild-type poliovirus in the country. Their analysis showed that this serotype 2 cVDPV is as easily transmitted and likely to cause severe disease as wild-type poliovirus of the same serotype.
The study also shows that vaccination with trivalent OPV, one of the main types of vaccine currently used to combat polio, is highly effective in preventing paralysis by this serotype 2 cVDPV.
The research shows that it is even more effective against cVDPV than against the wild-type polioviruses that are currently circulating, which can also be targeted with a different vaccine.
The new findings mean that it is particularly vital that efforts to vaccinate children with trivalent OPV continue in Nigeria and neighbouring countries, to protect children against all strains of polio. The scientists hope their findings will help countries to devise the right vaccine strategies to eradicate polio.
Helen Jenkins, the lead author of the study from the Medical Research Council Centre for Outbreak Analysis and Modelling at Imperial College London, said: “Our research shows that vaccine-derived polioviruses must be taken seriously and that we have the right tools to tackle them. We’ve had a lot of success against polio in the past and we’re optimistic that ultimately we should be able to eradicate it completely.
“However, our study shows that we can’t be complacent about the virus. It’s still vital for us to protect children from this dangerous and debilitating disease and we have to make sure we continue to vaccinate as many children as possible in affected countries for as long as wild-type poliovirus continues to circulate,” added Ms Jenkins.
Senior study author Dr Nicholas Grassly, also from the Medical Research Council Centre for Outbreak Analysis and Modeling at Imperial College London, added: “There has been some debate about the significance of circulating vaccine-derived polioviruses for the eradication initiative. Our research shows these viruses can be as pathogenic and transmissible as wild-type polioviruses and outbreaks must be responded to with just as much vigour.”
Dr Bruce Aylward, Director of the Global Polio Eradication Initiative at WHO, added: “These new findings suggest that if cVDPVs are allowed to circulate for a long enough time, eventually they can regain a similar capacity to spread and paralyse as wild polioviruses. This means that they should be subject to the same outbreak response measures as wild polioviruses. These results also underscore the need to eventually stop all OPV use in routine immunization programmes after wild polioviruses have been eradicated, to ensure that all children are protected from all possible risks of polio in future.”
This study was funded by the Medical Research Council and the Royal Society.
http://www.sciencedaily.com/releases/2010/06/100623190726.htm
Natural Solutions Foundation
The Voice of Global Health Freedom™
www.HealthFreedomUSA.org
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June 25, 2010
PUSH BACK Victory!
“Wall Street Reform” Bill to be Signed by President —
Does Not Include FTC Power Enhancement
We warned about the potential for a general grant of FTC “rule making” authority to restrict our access to natural solutions — to nutrients and remedies — under the guise of “consumer protection” which would create such barriers in the marketplace as to destroy the generally small producers of natural products.
The Wall Street Reform and Consumer Protection Act of 2009 (H.R. 4173), adopted by the House of Representatives and by the Senate as S.3217, could have include language — offered by Rep. Waxman [D – CA] — giving more power to the Federal Trade Commission to make “general rules” for interstate commerce that could have been used to restrict truthful information about dietary supplements, by requiring expensive, “drug company” level clinical trials before vitamin companies could make claims about their products. This “reform” could have handed-over the natural products industry to Big Pharma, which, over the past few years, has bought up most of the larger industrialized vitamin companies. The new rules could have been a “barrier against entry” driving many smaller companies out of business.
Instead, reports are, the final bill to be signed by the President does NOT include such general rule-making power.
Please continue to provide your generous support for efforts like this! We need your help and rely on it to achieve victories like this! http://drrimatruthreports.com/?page_id=189
Article on “FTC Denied Expansion of Powers” – http://www.nutraingredients-usa.com/content/view/print/309545
We’ve modified the original Action Item into a “thank you” to Congress: http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=3142
Natural Solutions Foundation
The Voice of Global Health Freedom™
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
June 24, 2010
Donate to keep health freedom free!
http://drrimatruthreports.com/?page_id=189
Click here to tell Congress that it is high time for a meaningful Congressional Investigation into the causes and cures for autism and other environmentally caused diseases: http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=3688
Important Note: Please share this as widely as possible
Could mercury be included in vaccines not in spite of its devastating whole-body, all-systems toxicity, but BECAUSE it it? Read what Dr. Paul G. King, http://www.Mercury-freeDrugs.org, has to say on the topic.
Dr. King is one of my favorite health heroes. He is a human being who thinks like a scientist and a scientist who thinks like a human being. He also possesses one of the most important qualities which anyone can exhibit: he is fearless. Using his well-honed scientific logic, he asks questions that may seem to be inconvenient of impolite and then uses logic and research to find the answers.
Does, asks Dr. King, the use of mercury (Thimerosal) make any sense in vaccines as a preservative and antiseptic since it is not an antiseptic, not a preservative, nor is it safe? No, it does not. So why, Dr. King asks, is it used? What could possibly explain the available data? Perhaps that data is explained by the unthinkable: that Thimerasol is included in vaccines precisely because it is a systemic poison.
That is a horrific and close-to-unthinkable idea unless…. unless you look at that data. The questions of why anyone would poison our children “unto the seventh generation” is not one that Dr. King takes up. I do. I maintain that the sustainability of the globalists, which they do so love to talk about, is their reason for poisoning us with vaccines, Codex-degraded foods, pollution, deadly medicines and, yes, vaccines.
But before you accept this horrifying proposition, please read Dr. King’s editorial closely and consider it for yourself. Then, whatever you decide, join us in taking the Action Item at the head of the page in which we are demanding of Congress that they hold a Congressional Hearing on autism and other environmental diseases.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Valley of the Moon™ Eco Demonstration Project
www.NaturalSolutionsFoundation.org
www.InternationalDecadeofNutrition.org
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Donate to keep health freedom free!
http://drrimatruthreports.com/?page_id=189EDITORIAL – 23-06-2010
Thimerosal in Vaccines: A ‘Profitable’ Medical Maiming Agent?
Introduction to Thimerosal, a Highly Toxic Organic Mercury Compound
Paul G. King, PhD
Since the mid-1800s, we have been, and are being, exposed to increasing background levels of elemental,
inorganic, and naturally occurring organic mercury.
However, the history of mercury-containing poisons turned much more deadly when people began to make
synthetic organic mercury compounds specifically designed to be more toxic [1] to life than the common environmental inorganic mercury compounds.
[1] On a relative scale where metallic mercury has a relative toxicity of “1”, inorganic mercury compounds typically are “10 times more toxic as a group and organic mercury compounds are “100 to 1000” times more toxic on a weight basis than metallic mercury.
It is against this background that a chemist, M. S. Kharasch, synthesized a variety of “alkyl mercuric sulfur”
compounds, including sodium ethyl mercuric thiosalicylate [2], in the 1920s.
[2] Based on recent studies, this compound is on a molar basis at least 10 times more toxic to developing neurons and astrocytes than the methyl mercury compounds found in fish.
In 1928, the US Patent Office granted Kharasch a patent (“Alkyl Mercuric Sulfur Compound and Process for Producing it. US Patent 1,672,615”), relating to this alkylmercury sulfur-containing compound, which he had synthesized in the laboratory, and to the process for producing it.
He assigned this patent, along with two follow-on patents: “Kharasch, M. S. 1932. Stabilized Bactericide and Process of Stabilizing it. US Patent 1,862,896” and “Kharasch, M. S. 1935. Stabilized Organo-Mercuri-Sulphur Compounds. US Patent 2,012,820”, to the company for whom he worked, Eli Lilly and Company (Lilly) [3].
[3] These patents clearly established the instability of water- containing solutions of sodium ethyl mercuric thiosalicylate such as those in vaccine formulations.
The “safety” studies Lilly-affiliated personnel conducted on this compound were limited to some cursory animal toxicity studies that killed many of the test animals, and a specious test on some patients dying from bacterial
meningitis in the days before modern antibiotics.
In spite of the obviously highly toxic nature of this mercury compound and its instability in water-containing solutions, Lilly chose to manufacture and market this compound under the trade name “Merthiolate” [4] in the 1930s.
[4] “Mer” from mercury and “thiolate” from thiosalicylate”. The other trade names for this compound include: Merfamin, Merthiolate sodium, Mertorgan, Merzonin, Merzonin sodium, SET, Thimerosal, Thimerosalate, and, principally in Europe, Thiomersal and Thiomersalate.
Lilly sold Merthiolate as a 0.1% alcohol solution [5] (Tincture of Merthiolate), which it promoted as a “safe” and “effective” over-the- counter (O-T-C) topical antiseptic.
[5] As studies conducted in the 1930s and 1940s clearly established, the only effective antiseptic was the alcohol in the tincture – Merthiolate/Thimerosal, ateven levels of 0.1%, was neitheran effective antiseptic nor bactericidal.
Lilly marketed this O-T-C antiseptic without any valid toxicological proof of either Merthiolate’s “safety” (or its “effectiveness” as an antiseptic beyond that of the alcohol in which it was dissolved) from the early 1930s.
It also used this compound, also trade-named Thimerosal, as a preservative in the serum and vaccine products Lilly sold until the mid- 1970s [6].
[6] When it exited the vaccines business in the mid-1970s, Lilly licensed the use of its proprietary processes for the manufacture of Thimerosal- preserved vaccines to other vaccine makers and, until 1994, continued to make the Thimerosal powder used in their manufacture.
In 1998, after decades of procrastinating, the US Food and and Drug Administration (FDA) banned the use of Merthiolate/Thimerosal and related mercury compounds as ingredients in the manufacture of O-T- C topical antiseptics and vaginal contraceptives.
The FDA banned these uses of these mercury compounds on the grounds that they were neither safe to be administered to humans nor effective as a bactericidal agent in such applications.
However, though the FDA recognized Merthiolate’s/Thimerosal’s lack of safety to humans at antiseptic levels (nominally, 0.1 % by weight/volume) and its failure to be an effective antiseptic or spermicide, the FDA continued to ignore the realities of Thimerosal’s toxicity when it is used in the making of prescription medicines, where it is used as a preservative and its nominal levels range up to 0.01% by weight/volume.
As of June 2010, the FDA continues to permit the use of Thimerosal in prescription drugs, including vaccines and other biological drug products.
Thus, without the required toxicological proofs of safety, Thimerosal is still being used in the manufacture of several FDA-
approved vaccines and other drugs.
From the early 1930s until the mid- 1970s, Lilly manufactured and distributed Thimerosal-preserved serums and vaccines under licenses granted by the US National Institutes of Health (NIH), which regulated serums and vaccines.
In the late 1960s, because of the NIH’s mismanagement of vaccines, the oversight for serums and vaccines was transferred to the FDA.
Unfortunately, this transfer of oversight to the FDA included the transfer of key individuals from the NIH to the FDA’s then “Bureau of Biologics”.
Among the transfers was the then head of this FDA bureau, who continued to allow the use of Thimerosal as a preservative in biologics without the required toxicological proofs of safety.
Since 1973, all Thimerosal-containing serums and vaccines for use in humans have been regulated as biologics (biological drug products) under Title 21 of the United States Code of Federal Regulations (21 CFR) in 21 CFR §§ 600 – 680, in specific, and under all of the applicable parts of 21 CFR, in general.
As of June 2010, the manufacturers who use it have apparently not proven that the use of Thimerosal as a “preservative” in such biological products is “safe” in the manner required by law.
This is the case because 21 CFR §610.15(a), the applicable current good manufacturing practice (CGMP) drug producer’s minimum nondischargeable “shall” compliance obligation, specifically requires: “Any preservative used shall be sufficiently nontoxic so that the amount present in the recommended dose of the product will not be toxic to the recipient” [7].
[7] Note: Scientifically, the dose of a compound is “nontoxic” when the maximum level present is properly proven to be below the compound’s NOAEL (no observed adverse-effect level) when, in the intended manner (injected in the case of vaccines), the appropriate animal surrogates for the most sensitive group for which the use of the compound is intended (for vaccines, the most sensitive groups are the fetuses of pregnant women and developing children) receives the maximum amount permitted in a single dose at a frequency that appropriately matches the maximum in the most sensitive group.
To be “sufficiently nontoxic”, as required here, the level of the preservative dose must be appropriately below the NOAEL by
more than one order of magnitude (> a factor of 10).
For example, if the NOAEL for injected Thimerosal in a vaccine formulation is about 0.01 micrograms/kg of body weight/per
day, then a maximum level of about 0.0001 micrograms/kg/day (a
factor of 100 lower) might be an appropriate to ensure that the dose delivered were “sufficiently nontoxic”.
The need for a safety factor of 100, or more, arises because of the highly toxic, bioaccumulative nature of Thimerosal and its metabolites. In most current Thimerosal- preserved vaccines, the nominal level of Thimerosal is on the order of nominally 100 micrograms per milliliter. Moreover, the developing fetus typically weighs in the range from less than 1 gram to no more than 6 kg.
Thus, it is obvious that Thimerosal is much too toxic for 0.5-mL injections into the pregnant woman (delivering nominally up to 50 micrograms of Thimerosal to the fetus) to be safe since the maximum level could exceed 50,000 micrograms of Thimerosal per kilogram of fetal weight during the early weeks of pregnancy!
Today, Thimerosal, sodium ethyl-mercurithiosalicylate, is a recognized human teratogen, mutagen, carcinogen,
immune-system disruptor, and reproductive toxin at levels well below 1 part per million (ppm).
With the preceding background in mind, let us consider the “criteria” for a profitable medical population-maiming
agent and then assess how well Thimerosal used as a preservative in vaccines meets these criteria.
The “Criteria” for a Long-term ‘Profitable’ Medical Population-Maiming Agent
1. Hidden sub-acutely toxic doses of the poison must be given to each cohort of developing children before, or shortly after, birth and periodically afterward in some medicine.
Ideally, for a mass poison that is intended to “permanently” maim, but not kill, many of those who are given it, the poison needs to be given as soon as possible to as many of the target population as possible – in all parts of the target country at about the same time.
Thus, when the target is humans, the first characteristic must be that, before birth or as soon as possible after birth, almost every child must be covertly exposed to a suitably “toxic” dose of the poison.
This non-lethal, sub-acutely toxic dose must be sufficient to slowly poison some small percentage of those given it in a manner that, over time, renders them chronically ill.
In addition, to maximize the cumulative profit, almost every child must be given multiple sub-acute doses
of this poison as he or she develops.
This tactic helps to ensure:
o The percentage chronically harmed will increase over time, and
o The general population will be slow to connect the harm done to the concealed poison repeatedly administered to the developing children.
2. The doses of the poison must be portrayed as contributing to the “safety” of the product in which they are placed and the public must consider the products containing the doses of poison to be “vital” for developing children to receive
To permit the poisoning to proceed for a long time before anyone starts to notice it, the population as a whole, an especially those administering the poisoning doses, must not notice the poison or, if they do notice it, perceive that the dose being given is an insignificant dose.
In addition, the poison should be presented as a contributor to the “safety” of the medical product in which it is delivered.
Finally, the poison should be concealed in a medical product that the public perceives, or is led to believe, is necessary or vital for most all children to receive.
3. Each small dose of the poison must cause chronic disease in some who are given more of it
The third key for an exquisite mass-use poison is that only a single small dose is required to cause long-term toxic effects in some, with successive doses causing increasing effects in an increasing percentage of the population.
4. The poison’s effects must be time delayed and/or slow to develop
The fourth attribute for a near-ideal mass poison is that its observable poisoning effects must be delayed and/or slow to develop so that the resulting poisoning is not closely associated with the maiming doses’ delivery.
5. The poison must be a systemic Poison
The fifth characteristic for a “ideal” mass poison is that it must be a systemic poison that affects all of the biological systems of the targeted population to varying degrees.
This ensures that the agent’s harm is harder to recognize because the poison’s effects are not be limited to
one specific organ (e.g., heart) or system (e.g., immune system).
6. When recognized, the poison must be difficult to remove and/or to reverse its ill effects
The sixth attribute for a mass poison designed to provoke chronic disease must be that, once the poisoning is
finally recognized, the poison’s final metabolic products must be bioaccumulative persistent toxins that are difficult to remove from the body or hard to neutralize – making the chronic effects difficult and/or medically costly to reverse.
7. The poison and/or its metabolites must be soluble in aqueous and non-aqueous systems
The seventh design parameter for an effective mass poison must be that the poison and/or its immediate toxic
metabolites are soluble in both aqueous (hydrophilic) and non-aqueous (hydrophobic) regions of the body to ensure that as many organs and systems as possible are adversely affected in as many manners as achievable in the target population.
8. The poison must induce multi-generational adverse genetic and/or epigenetic effects in some of those who are dosed with it
The eighth key characteristic is that the poison must have some probability that some of its adverse health effects will be passed on to some of the offspring that those who are directly poisoned may subsequently bear or father so that, even when the poison’s use is finally stopped, it will continue to generate chronic illness in some children for generations to come.
9. The Establishment must claim that the poison is “safe” and block the requisite toxicity studies that would prove it is not “safe”
The ninth key, for our ideal mass poison, is that the medical establishment, drug makers, health officials, all the relevant government agencies and the mainstream media must not only claim that this poison is “safe” at the level used but also
refuse to conduct, and/or otherwise block, the appropriate toxicity studies that would reveal its true
toxicity.
Thimerosal at Preservative Levels in Vaccines: An Ideal Poison for Medical Mass Maiming?
From the history of its discovery, isolation and characterization, it is clear that Thimerosal is not stable when dissolved in aqueous environments.
Then, why would any firm knowingly choose Thimerosal for use as a preservative in water-based (aqueous) vaccine formulations when it is unstable in aqueous solutions?
Moreover, if one were looking for a preservative that was “safe” and “effective”, why would a firm choose to use Thimerosal, a compound that:
o Becomes more toxic over time when dissolved in isotonic pH-buffered physiological saline, and
o Rapidly losses its effectiveness as a “preservative” in serums and vaccines, when exposed to common protein components present in such products?
Yet, Lilly used Thimerosal/Merthiolate as a preservative (nominally, at .01%) in its serum and vaccine products from the 1930s until the mid-1970s when it exited the vaccines business.
In addition, along with other firms, Lilly marketed Thimerosal as an O-T-C topical antiseptic (Merthiolate) until the late-1990s, when, on the grounds of a lack of safety and a lack of effectiveness unequivocally established in the 1970s, the FDA finally banned its use as an ingredient in such O-T-C antiseptics and vaginal contraceptives.
Further, the Thimerosal-preserved early childhood vaccines (like Lilly’s DT and DPT vaccines) appear to meet the first two criteria for a profitable population-maiming agent:
1. An early population-wide deployment that maximizes the profit potential, and
2. The concealment of an “inconspicuous” amount (1 part in 10,000) of the agent as a “helpful” substance (a “preservative”) in “life saving” vaccines given several times in early childhood.
Thus, besides Tincture of Merthiolate, touted as a “safe” and “effective” topical antiseptic but not universally used by pregnant women or on young developing children, the first Thimerosal-based mass-maiming agents deployed appear to be the injected Thimerosal-preserved DT and DTP Vaccines [8], which Lilly made for administration to babies several times before their first birthday.
[8] After Lilly exited the vaccine market, other vaccine makers, principally what is now Sanofi Pasteur and GlaxoSmithKline as well as other vendors have marketed Thimerosal-preserved vaccines including some that are still being manufactured to this very day and are approved for US use.
From the 1980s until the early 2000s, in addition to Thimerosal- preserved DT and DTP vaccines, Thimerosal-preserved Td, TT, Hib, Hep B, Meningococccal, Inactivated-influenza and other vaccines were approved for use in various population segments including, for the Hib and Hep B vaccines, children.
With the phasing out of the Thimerosal-preserved DTP, Hib and Hep B vaccines as well as the Thimerosal-preserved Rho(D) products given to Rh-negative women during pregnancy in the early 2000s, in 2002, the CDC moved to replace the lost Thimerosal-maiming doses with the mercury in inactivated-influenza shots to be given to pregnant women and children 6 months to 23 months of age. By steadily increasing the upper end of the age range for
the children until it was up to 18 years in 2009, recommending 2 shots the first time a child is vaccinated for influenza, and, in the 2009-2010 flu season, adding recommendations that included one Thimerosal-preserved inactivated- influenza 2009-A-H1N1 vaccine for pregnant women and two additional doses of what could be a Thimerosal-preserved 2009-A-H1N1 vaccine for children under 9 years of age and 1 dose for those over nine years of age, the CD has effectively more than replaced the mercury removed for most of the pregnant women and children because most doses of
the inactivated-influenza vaccines (nearly 100% in the 2002-2003 flu season, and at least 75% in the 2009-2010 flu season) were Thimerosal-preserved doses.
The CDC’s recommendation to give flu shots to pregnant women is particularly egregious because all flu vaccines are: a)
“Pregnancy Category C” drugs, whose fetal and reproductive safety and effects have never been properly established and b)
drugs that have also not been tested for mutagenicity and carcinogenicity.
These Lilly vaccines were touted as life saving drugs that “immunized” (bulletproofed) children from getting deadly diseases, diphtheria (D), tetanus (T), and pertussis (P; whooping cough), which were often fatal.
Moreover, each dose of these “preserved” vaccines directly delivered nominally 50 micrograms of Thimerosal (25 micrograms of organic mercury) – a level that is more than sufficient to cause a low-level of harm in susceptible babies [9].
[9] Based on the only FDA-recognized chronic rat study for injected Thimerosal, the “nontoxic” level for injected Thimerosal is somewhere below 0.0042 microgram of Thimerosal-derived mercury per kilogram per day [see:
http://mercury-freedrugs.org/docs/090812_fnldrft_TheTruthAboutTheToxicityOfThimerosalr5b.pdf,
“The ‘Truth’ About The Toxicity Of Thimerosal (12 August 2009; 6 pages)”].
Based on several independent retrospective statistical population records studies, an exposure increase of 200 micrograms of Thimerosal (100 micrograms of organic mercury) in children vaccinated during their first year of life has been proven to be a statistically significant, or nearly statistically significant, population risk factor for a variety of serious childhood medical conditions (e.g., autism, tics, and, most recently, premature puberty).
In some reported monkey studies, a single weight-proportional birth dose of a Thimerosal-preserved hepatitis B vaccine has been shown to cause subtle, but serious, adverse effects on their early development.
Thus, Thimerosal, at preservative levels in vaccines, appears to meet the third criterion.
Moreover, the principal persistent adverse effects, like loss of words, failure to thrive, tics, or premature puberty, that have been linked to Thimerosal exposure from the injection of Thimerosal-preserved vaccines, are delayed effects.
In most cases, the exposed infant in America appears to progress normally for some period after the initial or one of the subsequent poisonings (e.g., at 2, 4, and 6 months for the Thimerosal-preserved DTP vaccines up until 2004, or at before birth and 6 [and 7] months for the Thimerosal-preserved flu shots that the CDC started ‘encouraging’ healthcare professionals to give pregnant women and healthy babies in 2002) [10].
[10] Building on the DTP program, the Thimerosal exposures were increased to at birth, 2 and 4 to 6 months when the early hepatitis B program was introduced in the 1990s, in addition to 3 more doses (at 2, 4, and 6 months) from the Hib
vaccines introduced in the late 1980s.
Further, as the level of Thimerosal was being reduced in the early childhood vaccines, the CDC started making recommendations that pregnant women and healthy children at 6 to 23 months of age receive the Thimerosal-preserved inactivated-influenza vaccines in 2002.
Currently, the CDC recommends inactivated-influenza vaccination for pregnant women and children at 6 and 7 months and annually thereafter, where the majority (not less than 75%) of the available doses are Thimerosal-preserved. In addition, in 2009 the CDC recommended an additional 2009- A-H1N1 inactivated-influenza vaccine shot for pregnant women; two of these flu shots for children up to age 9; and one of these flu shots for those 9 and older – where most all of the available doses of the 2009-A-H1N1 flu shots were again Thimerosal-preserved inactivated-vaccine doses.
Then, the susceptible exposed infant begins to “regress” or “change” as the symptoms of the maiming become evident months (usually, at or after 1 year of age) or, in the case of premature puberty (and probably childhood MS), several years later.
Thus, Thimerosal clearly satisfies the fourth, “effects delayed and/or slow to develop”, criterion for an effective population-maiming agent.
Thimerosal clearly satisfies the fifth criterion because it is a proven systemic human poison at low levels (part-per million and lower).
For example, Thimerosal is a known human carcinogen, mutagen, teratogen, immune-system disruptor and reproductive toxin (by California Prop 65 criteria) at levels below 1 part- per-million (ppm) of Thimerosal in the body.
Further, Thimerosal’s end-product metabolites are tissue-bound inorganic mercury species that have human half- lives on the order of one to two decades, depending on the tissue.
Thus, it is clear that Thimerosal is a bioaccumulative persistent toxin.
Moreover, as studies in monkeys have established, the tissue-bound “inorganic mercury” species form faster when an ethyl mercury compound was administered than when a similar methyl mercury compound was administered.
In addition, even when aggressive “mercury chelating” agents, like DMSA and DMPS, are used, the level of mercury “bound” in the tissues can only be slowly reduced.
Typically, chelation takes years to significantly reduce the poisoned individuals’ body-burden of tissue- associated, “inorganic” mercury to the point that those reversible [11] symptoms induced by the mercury- poisoning events are minimized or, in some instances, are apparently eliminated.
[11] Unfortunately, unless tested for mercury toxicity and treated before the adverse effects produce persistent symptoms, some of the developmental harm done seems, at present, to be non-reversible in many
instances.
Thus, Thimerosal has the characteristics required for the sixth key attribute for a maiming poison because any exposure to it can slowly provoke a wide range of chronic adverse clinical conditions and its mercury containing end-point metabolites (tissue-bound “inorganic mercury”) are difficult to remove from the tissues in which they reside.
Further, when a Thimerosal-containing solution enters the human body, the Thimerosal present reacts with the body’s aqueous fluids to form the following organic compounds:
– Ethyl mercury chloride (EtHgCl), which is highly lipophilic (hydrophobic);
– Ethyl mercury hydroxide (EtHgOH), which is highly hydrophilic; and
– Sodium thiosalicylate, which is further metabolized in the body.
Since both of the initial ethyl-mercury-containing metabolites of Thimerosal are small neutral species, they:
– Are easily transported within the human body;
– Apparently cross or circumvent the blood-brain barrier and cross the placenta and enter the fetus; and
– Once inside a given tissue, are rapidly converted into tissue-associated “inorganic mercury” that tends to bioaccumulate in
that tissue.
Given the preceding realities, it is clear that Thimerosal and its mercury-containing metabolites directly and indirectly poison almost all human biological processes to some degree wherever a mercury species can interfere with the body’s fundamental systems.
Thus, Thimerosal’s rapid breakdown in the human body into small neutral mercury-poisoning metabolites (that are both hydrophilic and hydrophobic and which migrate into the tissues and are converted into tissue-resident “inorganic mercury”) satisfies the seventh criterion for an exquisite mass-maiming poison.
Further, based on multi-generational reproduction experiments done in the former Union of Soviet Socialist Republics (USSR) [12], sub-acute Thimerosal exposure is clearly capable of inducing epigenetic and/or genetic changes in the offspring who are exposed to Thimerosal in utero.
[12] Goncharuk GA. Experimental investigation of the effect of organomercury pesticides on generative functions and on progeny. Hyg Sanit. 1971; 36: 40-43.
The changes induced in utero were shown to be expressed in the non- Thimerosal-exposed second-generation offspring of the first-generation of indirectly exposed offspring.
Thus, Thimerosal, used as a preservative in vaccines, appears to be a multi-generational poison.
Moreover, these experimental findings help to explain why the then USSR, already experiencing a population decline, was the first European nation to ban the use of Thimerosal in vaccines (in the early 1980s) – more than 2 decades before the US finally began slowly reducing the level of Thimerosal in the previously Thimerosal preserved early childhood vaccines.
While, obviously driven by other imperatives, the FDA continued to approve additional Thimerosal- preserved vaccines (e.g., the vaccines for hepatitis B and Haemopholis influenza type B) and the Centers for Disease Control and Prevention (CDC) continued to add these additional FDA-approved Thimerosal-preserved vaccines to the recommendations for the national childhood vaccination program.
Thus, Thimerosal apparently meets the eighth key attribute for a near-ideal population-maiming toxin – its maiming effects can be transferred to the offspring of mothers who were themselves exposed during pregnancy as long as these in-utero-exposed ‘potential mothers’ are not so damaged that they are “miscarried” or they cannot bear children.
Finally, given:
-The official positions taken by the medical establishment, the vaccine makers, the health officials, academia, all relevant governmental agencies and the mainstream media that the use of Thimerosal as a preservative in vaccines is “safe” and
-The refusal of all to conduct (or report to the public) all of the applicable toxicity studies required to prove that this use of Thimerosal is “safe”,
Thimerosal clearly satisfies the ninth key factor for a near-ideal population-maiming poison that is touted a “beneficial” component (a preservative) and added to “life saving” vaccines that all American children are recommended to be repeatedly
given.
Thimerosal at Preservative Levels in Vaccines: A Near-ideal Medical Agent for ‘Profitable’ Mass Maiming
Thus, Thimerosal’s use as a “presser- vative” in medical vaccines seems to meet all nine (9) of the criteria for a ‘profitable’ medical mass-maiming poison.
Further, it seems clear that Lilly and the current vaccine manufacturers, which, without complying with 21 CFR § 610.15(a), continued to use Thimerosal as a preservative in vaccines and/or to
apparently profit from its on-going use, have been knowingly engaged in the apparent medical poisoning of
American children for decades in order to, at some point, profit over several decades from the Thimerosal-induced increase in the level of children in the USA who have life-long chroni health conditions (e.g., for ‘autism’, from less than 1 in 1000 children born in 1955 to more than 1 in 100 born in 2005; and, for asthma, from less than 1 in 1000 children in the 1950s to greater than 1 in 10 born in the 21st century).
Finally, these actions have apparently been, and are still being, undertaken with the tacit consent and/or assistance of all the Thimerosal-use-sup- porting facets of the Establishment.
Disclaimer
**************************************
* The information provided in this editorial is just that-information. *
* It is not medical advice and it does not require any specific action or actions. *
* While the statements made are thought to be accurate, no representations are made as to their accuracy other than that they are my best understanding of the facts on the date that this editorial was first published on the Internet. *
* All should verify the accuracy of the information provided for themselves before acting on it or reacting to it.
**************************************
Concluding Remarks
Should any reader find significant factual errors in this editorial, then please send the author (at drking@gti.net) your proposed changes along with e-mail attachments that contain copies of the published documents that provide the proofs needed to substantiate your claims.
Then, as has been the case in the past, after verifying the validity of your concerns, the confirmed factual errors will be corrected and an appropriately “revised editorial” posted.
If you find spelling, grammar or textual errors, please also send them in so that this document can be appropriately revised and posted as an “updated editorial”.
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THE ONE WITH THE BEST SONGS WINS!
FREEDOM STRUGGLES ARE NEVER WON WITHOUT MUSIC. Music takes the concepts of freedom, lubricates it and inserts it directly into the head and the heart. And it is the head and the heart of the people where battles and wars seeking freedom are won. So the Natural Solutions Foundation is taking two steps: first, we have a contest in which your musical and artistic setting of the song I wrote (see below) will be shared with every one of our supporters around the world. Second, we are asking you to perform and share your music and art with us. The rules for sharing your artistic creation with the Natural Solutions Foundation are the same: All decisions are final and all entries are the property of the Natural Solutions Foundation. Entries will be judged on creativity and musical and visual originality.
CONTEST: Set the Song of the Uber-Cartel to Music, make a You Tube video (10 minutes or less) and email it to me at releyes@gmail.com. If your entry is selected, it will be mounted on the Natural Solutions Foundation You Tube channel, www.Youtube.com/naturalsolutions and we’ll feature it on our home page and in a blast! All decisions are final and all entries are the property of the Natural Solutions Foundation. All decisions are final. Entries will be judged on creativity and musical and visual originality.
Bill and Melinda Gates head the largest foundation in the world. Billions of dollars in assets allow Mr. and Mrs. Gates to do whatever good works they choose. The good works seem to be to finish what the Nazis started, but what they lacked the resources to finish: purification of the race. Bill Gates is using his unfathomable wealth to dominate and destroy the world’s population, and he does so right out in the open.
Bill Gates is not the only genocidalist out there: indeed there are a large number of wealthy, influential and powerful people who think that using one set of characteristics or another you can identify the people that you want to be rid of and justify the slaughter of every man, woman and child of the others. The word for that behavior is “Genocide”. Mr. Gates thinks that it is a really good investment.
I sing songs that the the story of struggles to stay alive and lives in other times, other places, but sharing the essential emotions and capacity of being human: I am an unrepentant “folkie”, guitar, banjo, and concertina and all. But I know of no song for a conscious and cold blooded genocialist. I therefore felt that I had to write one.
The following song is a dialogue between Mr. Gates, aged and near death, and his (in actuality, non-existent son). In the song, Bill’s grandfather passed the message to his son and, in turn, Mr. Gates hears it and takes it to the people. All is, however, not lost: Pushback does work!
The Song of the Uber-Cartel needs a melody and some production, which I most definitely do not have time to do. So here’s a neat way to win a 1000 Gift Certificate for www.Organics4U.org, our Organics-only virtual mall! Just send your completed entries to me at releyes@gmail.com.
Headline: Bill Gates To Attend 2010 Bilderberg Conference
Microsoft founder who bankrolls sterilization vaccine programs to give speech on global warming agenda and “the needs of the poorest”
http://www.prisonplanet.com/bilderberg-2010-prisonplanet-com-master-page.html
Headline: Gates Foundation Researches Nanoparticle Vaccines Triggered by Sweat
LONDON — The Bill & Melinda Gates Foundation today announced 78 grants of US$100,000 each in the latest round of Grand Challenges Explorations. Grants include the development of a low-cost cell phone microscope to diagnose malaria, study of the strategic placement of insect-eating plants to reduce insect-borne diseases, and investigation of nanoparticles to release vaccines when they come in contact with human sweat.
http://www.infowars.com/gates-foundation-researches-nanoparticle-vaccines-triggered-by-sweat/
Headline: Sonic Male Sterilization Program Funded by Bill Gates
Gates recently announced that he would be funding a sterilization program that would use sharp blasts of ultrasound directed against a man’s scrotum to render him infertile for six months. The Bill and Melinda Gates Foundation is gaining a reputation for funding technologies designed to roll out mass sterilization and vaccination programs around the world. One of the programs recently funded by the foundation is a sterilization program that would use sharp blasts of ultrasound directed against a man’s scrotum to render him infertile for six months. It might accurately be called a “temporary castration” technology.
http://www.naturalnews.com/028853_ultrasound_fetus.html
Headline: Gates Foundation Funds Research to Turn Mosquitoes Into Flying Syringes
October 22, 2008 — The Bill and Melinda Gates Foundation awarded 100,000 dollars each on Wednesday to scientists in 22 countries including funding for a Japanese proposal to turn mosquitoes into “flying syringes” delivering vaccines.
http://afp.google.com/article/ALeqM5i4hpnz5eOMpxfld81tEZYsC23teg
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
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Song of the Uber-Cartel
Dedicated to Bill Gates
Rima E. Laibow, MD
June 5, 2010
Intro (Recitative):
I’m getting old, my Son, my days are nearly done and I want to leave this world with nothing left undone.
But my time is running fast and each breath may be my last, so I’ll give you now the gift my Dad to me once passed.
The plan for us is global (some would say, “ignoble”), but the world’s judgment moves us not at all
For centuries we’ve labored to create the world WE favor where our rule is total, and the population small.
We, the New Aristocrats, have no need of teeming peasant brats: they add nothing to mix and use our oil
For the culling is beginning
Our heady plans are spinning
Generations underground, then we rebuild the world we’ve so carefully despoiled.
So take, my Son, our message to the lowly, Useless Eaters of the globe. We, the Masters of the World,
Need only wait a few more years and then there will be none to carp or criticize or peer
Into our rule. Those alive will be our abject slaves. You, among the Masters, reigning evermore through all the coming years.
Uber Cartel Song To The People:
Uber-Cartel wants you to “mach schnell”, German for “hurry up now, my friend”
Diet of death, GMOs straight from hell. Pay us, we’re the piper, piping straight to the end
Too sick to be free, you can only agree: when the bell tolls, it tolls your death knell.
The game is an old one: steal and lie, cheat and kill for gold, glory, land, and total control.
Why waste bullets, purveying ill will, Bill, when you can be loved for your generous soul?
Flying syringes, food that impinges on their immune systems – Just sell them a pill.
Media’s message is “We’re here to help, to bring you the truth, tell you all that you need.”
Reality, though, says, “Don’t let the bitch whelp! Excess useless eaters like animals breed.
Make ‘em all sterile, still alive at their peril, sub-humans all, you just can’t see their pelt!”
We, the Masters, the Ubermenschen* free, have been raised up by God to rule and despoil.
Nine tenths are useless, slaves all the others be. With so few remaining, the earth’s ours to soil
Aristocrats, Neo,
Oh! Once we are free,
Oh! Glory to all, but most of all, ME!”
The doctor standing by heard the plans set to try, realized he, and those loved were all slated to die
When his needful task was done, he called the cell phone of his son, saying “Son, the truth must be revealed or we’ll in the dying try.
The globalists intend to cull us all to end our freedom and our lives, instead to spend our wealth themselves.
Served well by servants, techs, cooks, merchants whose lives on pleasing all their Masters will depend.
But that’s not the bargain free mankind accepts. Their blueprints have been marked and they’ve trained up their adepts.
We are the People, neither burden beasts nor sheeple: we hold freedom’s promise beating in our hearts.
Ring the loud alarm bells, spread the truth well, shine freedom’s light and tell the words of might
Widely in each church, each school and house. Saddle up and mount your fearless Freedom Mouse
Ride it straight to freedom ‘gainst the genocidal plan. Global freedom’s singing to each woman and each man!
*Ubermenschen: German for Superior People, e.g., Master Race
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Should the US Government Continue to Participate in Codex Alimentarius?
Health Freedom Supporter Survey…
http://salsa.democracyinaction.org/o/568/t/1128/questionnaire.jsp?questionnaire_KEY=1042
New Action item to STOP the fake food safety bill, S510 –
http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=4252
Here’s Dr. Rima’s View on Getting the US Out of Codex
http://www.youtube.com/watch?v=AfCni-LuR_c
Natural Solutions Foundation has been an unofficial observer at many Codex Alimentarius (World Food Code) meetings world wide over the past half decade. Our presence and reports on YouTube and elsewhere have made this previously little-known UN Commission – and its degradation of the world’s food supply – a matter of intense discussion among health freedom advocates all over the world.
The US is the strongest force, and the biggest bully, in Codex. But the presence of the USA in Codex is not necessarily a positive thing, on at least two levels. On one hand, the US Government, expressed by the FDA, has a stated policy of “HARMonizing” our nutrient freedoms with international restrictions, including restrictions inherent in Codex’s insistence upon treating dietary supplements as though they were industrial toxins, while allowing all sorts of real toxins into the food supply, denigrating natural and organic products. This “HARMonization”, however, is illegal according to several statutes passed by the US Congress.
On the other hand, the presence of the US delegation, with its heavy Big Agra, Big Chema, Big Biotech and Big Biz presence, tilts the Codex process away from natural, local and sustainable food production, leading to global industrialization and degradation of the food supply, mandated under-nutrition and a host of other serious ills, creating massive food borne illnesses: Cancer, Cardiovascular Disease, Stroke, Diabetes, Obesity and a host of others from which we are dying.
So the US presence may benefit neither the American people or the people of the rest of the world.
What do you think?
Take the Natural Solutions Foundation Survey to Express Your Opinion Here:
http://salsa.democracyinaction.org/o/568/t/1128/questionnaire.jsp?questionnaire_KEY=1042
Please share this post widely so that others can tell us if they think that the US should get out of Codex.
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Health Freedom IS our First Freedom,
Yours in health and Freedom,
Natural Solutions Foundation Trustees
Maj. Gen. Albert N. Stubblebine III (US Army, Ret.)
President
Rima E. Laibow, MD
Medical Director
Ralph Fucetola, JD
Counsel and Trustee
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