Archive for Swine Flu – Page 2
Natural Solutions Foundation
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June 24, 2010
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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
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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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Click here: http://drrimatruthreports.com/?page_id=189. Dr. Rima discusses the new “pandemic” fungus and how to respond to this latest threat from an eco system under severe man-made stress. Yet another “weaponized” pathogen and Nano Silver…
Health Freedom Thought Experiment.
The article following this essay looks at an emerging danger, the newly virulent Cryptococcus gatti fungus. Apparently weaponized, this may be “The Next Big Thing” for the genocidalists at WHO and elsewhere. If so, we need to have a defensive strategy and an offensive one as well.
I believe that the defensive one is to have as much high quality Nano Silver on hand as you estimate you will need both for immediate use and for what comes next, and next, and next again after that. Because it appears that the plagues manufactured in laboratories will keep coming. Nano Silver, like the Silver Solution we recommend, www.Nutronix.com/naturalsolutions will keep you safe if you have it and if you use it.
The offensive strategy is two fold: protect our health options and expose the genocidal agenda at every turn, making it so widely understood that the secrecy which allows it to function is shattered. Make the myth of overpopulation a thing of the past, like the myth of necessary female circumcision or a flat earth.
Let’st hink this through. What happens if we protect Nano Silver? What happens if its use in animals and humans is so widespread that it eliminates antibiotics altogether?
Physicists use “thought experiments” to guide them to new approaches when the experiment is too hard, too expensive or too novel to actually conduct. By working through the experiment in their minds, they can make [very] educated guesses about what happens next if they were to conduct the experiment in the real world.
Health Freedom can use the same techniques to conduct an important Thought Experiment. First, the propositions and assumptions:
Antibiotics and Vaccines
1. Antibiotics, vaccines and other pharmaceuticals are astonishingly profitable
2. Antibiotics are widely understood to be overused, leading to drug resistant and multiply drug resistant pathogens.
3. Vaccines have never been tested in a placebo controlled, double blind study to show that they are effective in either preventing or treating any disease. Vaccine manufacturers and regulators hold the position that it would be “unethical” to deprive the test subjects of the benefits of vaccines even though such benefits have never been rigorously documented while vaccine dangers have been.
4. 90% of all antibiotics used world wide are used in factory farming.
Nano Silver
1. Nano Silver is the Universal Antibiotic because laboratory tests show that it is effective against every disease-causing organism against which it has been tested: bacteria, mycoplasma, fungus (i.e., mold), virus. In all, It has been tested against more than 630 disease organisms and the result is the same: Low concentrations of Nano Silver kills disease-causing organisms. In addition, Nano Silver:
a. Is non-toxic to the environment and to living organisms since it leaves coalesces into larger ionic units which have no biological impact once it leaves the body
b. Leaves the body rather than accumulating in it due to its ultra-small size making overdose impossible
c. Cannot lead to the generation of new super bugs even with wide spread use since its mechanism of action does not permit organisms to develop resistance
d. Is inexpensive and has an indefinite shelf life, requires no refrigeration or other special care
e. Is self sterilizing, automatically killing disease causing organisms if it is contaminated by them
f. Is safe and effective for use in people of every age and condition and animals of all types
g. Has no known side effects
h. Does not kill beneficial bacteria leaving both gut and skin pro-biotic organisms intact while killing pathogens
i. Boosts white blood cell function, providing enhanced immune response
The Experiment: If Nano Silver were widely available, what would the results be?
1. Drug resistant organisms would no longer emerge in human or animal reservoirs
2. Resistant organisms in humans and animals would be killed off by the use of Nano Silver when they created disease. Over time, their numbers would decrease and the impact of disease from them would be either greatly reduced or eliminated
3. No new drug resistant organisms would emerge through the use of Nano Silver since its mechanism of action makes the acquisition of resistance impossible except through horizontal gene transfer. Any such organisms would be killed if they caused disease in humans or animals since they would be treated by Nano Silver.
4. Animals consumed for food would be significantly less toxic since Nano Silver, unlike the metabolites (by products) of antibiotic metabolism, does not remain in the body of either humans or animals
5. The amount of antibiotic and vaccine residue in effluent water and soil would decrease dramatically with marked environmental and health benefits since metabolites of drugs from the urine and feces of antibiotic and vaccine treated animals and humans poses and increasing health and environmental danger
6. Finely divided silver (without biological effect) would increase in effluent water and soil. This poses no known health or environmental danger.
7. The cost associated with antibiotic and vaccine therapy in humans and animals would be eliminated, to be replaced by a significantly lower cost
8. Pharmaceutical profits would drop dramatically since these two classes of drugs account for many billions of dollars of profit
9. Government and Union pension plans, as well as mutual funds, would loose value since they are heavily invested in major pharmaceutical stocks
10. Investing officers of pensions and mutual funds would seek other lucrative investments, including alternative energy and Advanced medicine options and companies, many of which have difficulty finding funding at this point because of the heavy investment in pharmaceutical and related, drug-based industries
11. Morbidity and mortality from nosicomial (hospital-acquired) infections would drop precipitously, eliminating a major health and health cost problem:
In the US in 1992, there were about 2 million nosicomial infections per year, =166,666 per month = 38,461 per week = 5,479 per day = 228 per hour =3 per minute. http://www.wrongdiagnosis.com/n/nosocomial_infections/stats.htm
Note: this equals approximately 10% of American hospital patients (CDC/NNIS 1992)
In 2004, 13% of all patients who acquired nosicomial infections died.
10. Nearly 100,000 people in the US alone would not die because nosocomial infections would be wiped out. “In the United States, the Centers for Disease Control and Prevention estimates that roughly 1.7 million hospital-associated infections, from all types of bacteria combined, cause or contribute to 99,000 deaths each year.” Pollack, Andrew. “Rising Threat of Infections Unfazed by Antibiotics” New York Times, Feb. 27, 2010
11. National, local and private health care costs would drop dramatically since the costs associated with antibiotics, vaccines and health care costs for infections would drop dramatically as well. In 2007, the direct costs of nosicomial infections Applying two different Consumer Price Index (CPI) adjustments to account for the rate of inflation in hospital resource prices, the overall annual direct medical costs of nosicomial infections to U.S. hospitals ranges from $28.4 to $33.8 billion (after adjusting to 2007 dollars using the CPI for all urban consumers) and $35.7 billion to $45 billion (after adjusting to 2007 dollars using the CPI for inpatient hospital services). (Costs of Hospital Acquired Infections in U.S. Hospitals Report,The Direct Medical Costs of Healthcare-Associated Infections in U.S. Hospitals and the Benefits of Prevention PDF 835 KB/16 pages, http://www.cdc.gov/ncidod/dhqp/)
12. Any pandemic, plague, or epidemic, whether intentional or unintentional, would be successfully halted by the universal application of Nano Silver orally.
13. Globalist plans for depopulation would be adversely impacted since communicable disease, including weaponized viruses, bacteria, etc., would be ineffective against a population supplied with Nano Silver.
14. Vaccine deniers would increase in number since epidemic diseases would be a thing of the past.
15. Globalists and their supporters would have to resort to means other than infectious agents, deadly drugs and dangerous, immune compromising vaccines to reduce the population. The 10-15% of the population which Bill Gates stated in a recent TED lecture could be eliminated through properly used vaccines would not die.
16. The myth of over population would suffer serious damage as the world population did not devour the available resources and the false mathematical and social engineering premises upon which it is based would be visibly flawed. See “Overpopulation, the Making of A Myth”, http://simranjeet.com/).
17. Local, clean and unadulterated food production could be instituted around the globe to enhance the health of people no longer dying from communicable diseases and parasites.
18. Chronic and deadly diseases like malaria, dengue fever, elephantiasis, tuberculosis, HIV and a host of others will become easily curable diseases.
19. Economic productivity and prosperity of poor and ill countries will rise as personal productivity increases due to decreased health care giver requirements and decreased time away from job and school.
20. Decreased overall health costs locally, nationally and internationally reversing some of the crushing burden of modern health costs through decreased hospital stays, increased infectious disease self care (fewer doctor and hospital visits and services), decreased drug and drug complication costs, less time away from job and school).
21. Increased Happiness Index, which is directly related to subjective (and, to a lesser degree, objective) measures of health.
21. Antibiotic and vaccine manufacturers will counter the loss of their market by political, propaganda and economic thrusts designed to eliminate Nano Silver. These will include
– Criminalizing and banning Nano Silver (already accomplished as of January 1, 2010 in the European Union and underway in the US)
– Deceptive science to “show” that the product is dangerous or ineffective
– Media campaigns to deride and/or demonize Nano Silver.
I think that covers most of the major impact of making Nano Silver widely and easily available. You have the good (health, autonomy, cost), the bad (pension and stock market impact) and the ugly (intentional, weaponized pandemics would be totally ineffective if they were based, as they have been to date, on infectious disease agents).
The net result? Stock up on Nano Silver, which we believe to have an indefinite shelf life.
We recommend the Silver Solution Nano Silver available at www.Nutronix.com/naturalsolutions because we believe that it is of exceptional quality and utility.
But whatever Nano Silver you choose to purchase, make sure that you have a good supply on hand. The apparently bioengineered Cryptococcus gatti fungi may be upon us as the next plague. MRSA may be the next plague. The next plague may be one that we have not heard of yet, but which has been in the works for years. Who know? Well, actually, it is very likely that WHO does know. But Nano Silver simply eliminates the threat of an infectious danger, IF you have it on hand and take it when the time is ripe.
I do. I hope that you do, too.
Yours in heath and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
The Dr. Rima Network: www.DrRima.net
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Health Freedom Virtual Mall
www.Organics4U.org
www.NaturalSolutionsMarketplace.org
Valley of the Moon BeyondOrganic Coffee
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TUESDAY 11 MAY 2010
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Mystery Disease Linked to Missing Israeli Scientist
Friday 07 May 2010
by: H.P. Albarelli Jr., t r u t h o u t | Report
(Photo: chickeninthewoods; Edited: Lance Page / t r u t h o u t)
Media outlets across the Northwest United States began reporting on April 24 that a strange, previously unknown strain of virulent airborne fungi that has already killed at least six people in Oregon, Washington and Idaho is spreading throughout the region. The fungus, according to expert microbiologists, who have expressed alarm about the emergence of the strain, is a new genotype of Cryptococcus gatti fungi. Cryptococcus gatti is normally found in tropical and subtropical locations in India, South America, Africa and Australia. Microbiologists in the United States are reporting that the strain found here, for reasons not yet fully understood, is far deadlier than any found overseas.
Physicians in the Pacific Northwest are reporting that an undetermined number of people in the region are ill from the effects of the strange strain. Physicians also say that the virulent strain can infect domestic animals as well as humans, and symptoms do not appear until anywhere from two to four months after exposure. Symptoms in humans include a lingering cough, sharp chest pains, fever, night-sweats, weight-loss, headaches and shortness of breath. The strain can be treated successfully, if detected early enough, with oral doses of antifungal medication, but it cannot be prevented, and there is no preventative vaccine. Undiagnosed, the fungus works its way into the spinal fluid and central nervous system and causes fatal meningitis.
The estimated mortality rate is about 25 percent of 21 cases analyzed. Several newspapers and media outlets in the US and overseas quote a researcher at Duke University’s Department of Molecular Genetics and Microbiology, Edmond Byrnes, as stating: “This novel fungus is worrisome because it appears to be a threat to otherwise healthy people. Typically, we see this fungal disease associated with transplant recipients and HIV-infected patients, but that is not what we are seeing.”
Microbiologists and epidemiologists studying the strain say the mystery fungus came from an earlier fatal fungus that was first found on British Columbia’s Vancouver Island in the fall of 2001, and perhaps as early as 1999. There the fungus infected and killed dogs, cats, horses, sheep, porpoises and at least 26 people. The disease spreads through spores carried by breezes and wind and when people and animals encounter infected ground where the fungus is present. A number of microbiologists say that the disease has “the potential to essentially travel anywhere the wind or people can carry it.” Reads an alarming study authored in part by Duke University’s Edmond Byrnes: “The continued expansion of C. gatti in the United States is ongoing, and the diversity of hosts increasing.”
Several researchers in California also note that the Cryptococcus gatti fungus has been researched for decades, extending back to the 1950’s, at the US Army’s biological warfare center, Fort Detrick, in Frederick, Maryland. One microbiologist at the University of California at Los Angeles recounted that the fungus was first brought to the attention of Fort Detrick researchers by British scientists experimenting with the bark of eucalyptus trees from Australia. Army biological warfare reports obtained through the Freedom of Information Act reveal that beginning around 1952 the Army mounted a huge research program involving numerous plant and fungi products, and that well over 300 long-term contracts and sub-contracts were let with over 35 US colleges and universities to carry out this multifaceted research. Examples of this early research in California included experiments and projects at Camp Cooke; Port Huemene; Harpers Lake; Oceanside, and extensive experimentation with wheat stem rust and “various spores” including “several from tropical locations” and cereal rust spores and dyed Lycopodium spores. Several Army reports reveal that private-sector corporations that participated or assisted in these projects were the American Institute of Crop Ecology; the American Type Culture Collection Inc.; University of California; Bioferm Inc. and the Kulijian Corporation.
The same microbiologist, who declined to speak on the record and who recounted extensive fungus work at Fort Detrick, also stated that researchers at Israel’s Institute for Biological Research, located in Ness-Ziona about 20 km from Tel Aviv, have worked with the Cryptococcus gatti fungus. They also report that mysterious Israeli-American scientist Joseph Moshe, 56 years old, may have conducted covert studies with the fungus while he was recently living in California. This report concerning Moshe is especially interesting because Moshe was briefly in the international spotlight in 2009 when he was the subject of a spectacular chase and arrest by the LA police department and SWAT team, assisted by the FBI, Secret Service, CIA, US Army and several other unidentified federal officials. That highly unusual arrest has never been fully explained to the media, and the whereabouts of Moshe has remained unknown since its occurrence. Compounding the mystery surrounding the Moshe case is that there is another scientist named Moshe Bar-Joseph who works in Israel and who looks remarkably like Joseph Moshe, except that he is about 20 years older.
Why Moshe was pursued and apprehended by the police is a largely unanswered question. According to the Los Angeles media, which recorded the entire incident by helicopter and ground cameras, Moshe claimed to be “a former Mossad microbiologist” who had telephoned a police dispatch number before his pursuit and had made “threatening statements about the White House and the president.” Reportedly, Secret Service spokesman Ed Donovan confirmed this when he spoke with several Los Angeles reporters.
On August 14, 2009, several Los Angeles police cruisers and an unmarked armored vehicle pursued Joseph Moshe as he drove his red VW automobile several miles through downtown Los Angeles before his car’s engine was reportedly knocked out by an electromagnetic pulse. Moshe refused to exit his car when ordered several times by the police, and after the driver’s window of his VW was smashed out by a robotic arm and several rounds of tear gas and pepper gas were fired into the vehicle, he still remained behind the wheel, refusing to move. At the time, police officers on the scene were stunned that Moshe was able to withstand three tear gas shells and hosing with pepper spray without moving. Later that day, a Los Angeles law enforcement official said: “I can’t explain that; there’s no way to explain that.”
After his apprehension, Moshe was taken to the Patton State Mental Hospital and then to the Twin Towers Correctional Facility in Los Angeles. Sometime about 60 days later, Moshe was quietly released and his current whereabouts are unknown. Since his arrest became public, reports about Moshe’s activities in the US have spread like wildfire, especially across the Internet. Many of these reports are unconfirmed, but a few come from credible sources and have linked Moshe to the grossly under-reported outbreak of flu in the Ukraine.
Other reliable sources, including two former Fort Detrick biochemists, have also linked Moshe to a mysterious disease that is becoming alarmingly common in Vermont and other states, including California. The disease is known to have killed or incapacitated at least 10 to 20 rural dwellers and farmers. This disease is said to be Morgellons disease or “a rare, mutated form of Morgellons disease.” Former Fort Detrick scientists, speaking off the record, say that the disease is one that was “experimented with intensely” in the late 1960’s at several “test sites in New England.” Morgellons causes patients to suffer horrible skin problems as well as fatigue, confusion and serious memory problems, as well as joint pain and the strange sensation that pins and needles are piercing the body or that something is crawling beneath one’s flesh. Some researchers and physicians believe that Morgellons is actually a psychiatric condition called “delusional parasitosis.” Other physicians, who are familiar with treating the disease, say it may be caused by “an airborne, unidentified spore” and that it was developed in the laboratory from an affliction that was first identified in the 1700’s. Regardless of its origin, some researchers say that Morgellons is becoming “a very real medical problem in some parts of the country.”
This work by Truthout is licensed under a Creative Commons Attribution-Noncommercial 3.0 United States License.
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Dr. Rima Reports: Guests
Due to Continual Interference with the Program, we are refraining from announcing guests in advance.
Here are some of our recent guests:
October 31, 2010: General Bert and Tim Bolen — www.BolenReport.com — on What is to be Done? Strategy for Health & Food Freedom in the Months Ahead…
October 24, 2010: Larry Becraft Esq. and Dr. Paul G. King on Recent Vaccine Litigation
October 17, 2010 – Mark Lerner- Opposition to Real ID – http://stoprealidcoalition.com/
October 10, 2010 – Eileen Dannemann – Vaccine Liberation Army – http://vaccineliberationarmy.com/
October 3, 2010 – Dr. Paul G. King PhD – http://dr-king.com
http://dr-king.com/docs/091230_NOTE_Autism&MercuryInCurrentVaccinationPrograms_b.pdf
September 26, 2010 John D. Crockett – www.MagicSoil.com
September 19, 2010 – Mike Adams, the Health Ranger: www.NaturalNews.com
September 12, 2010 – Charlotte Gerson- daughter of Dr. Max Gerson
September 5, 2020 – Karma Singh — Karma Healer — discusses healing energies with Dr. Rima
See: http://drrimatruthreports.com/?p=6152 for some of Karma’s energy transmissions.
Also, Nicholas Cremato tells us about the Natural Solutions PEL Seminar and Webinar on September 19th in NYC — “Find Yourself, Map Included…” — see: http://drrimatruthreports.com/?p=6330
August 29, 2010 – Dr. I.C. Rose: Changing Mindsets – Workable Solutions…
http://www.youtubesnips.com/user/icdrrose
August 22, 2010 – Inaugural Program.
Please Donate to Keep Us On The Air:
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http://vitaminlawyerhealthfreedom.blogspot.com/2010/01/ny-nj-reinstate-flu-vax-mandate.html and also at: http://www.campaignforliberty.com/blog.php?view=31477
NY & NJ Reinstate Flu Vax Mandates!
As the New Year starts and while both FDA and CDC try to frighten us with no-longer believable “Swine-Flu-Pandemic Third Wave” tales…
“And you old folks, don’t forget to get your jab! The government pays for it!” But, weren’t older folks supposed to have had some immunity to the “Swine Flu” from having lived through the 1976 “Swine Flu” fiasco? Isn’t that why it was children and pregnant women first to be “offered” the vaccines? And then health care workers, such as the New York plaintiffs in our “Stop the Shot” lawsuit.
You may recall that federal law suit ended when the New York health care worker flu vaccine mandate itself was suspended for alleged lack of vaccines. No vaccines, no mandate; no mandate, no court case.
See: http://drrimatruthreports.com/?p=3933 [Video Report]
Well, they’re back! “Governor David A. Paterson today announced that the State Department of Health (DOH) is reinstating the requirement that hospitals offer the H1N1 flu vaccine to the caregivers of newborns in intensive care and hospital patients who are 65 years of age or older. The reinstated requirement was made possible by increased supplies of vaccine.” [While the present and future scope of the reinstatement of the suspended mandate is not clear, it covers at least health care workers in newborn IC and older patients; possibly the parents of infants in IC as well.]
See: http://www.state.ny.us/governor/press/press_01151002.html
Looks like the intrepid NY health care workers who, since their initial victory over the NY mandate, have made common cause with others concerned about vaccination, may need to return to the Washington DC court, where the Federal judge told them at their hearing on November 2, 2009, if the mandate was reinstated, they could come back to him.
Meanwhile, the New Jersey licensed childcare attendance mandate has also come back into effect. NJ was the only other state-wide flu vaccine mandate in the US. It had also been suspended for alleged lack of supply (curiously just as we were seeking to amend the Complaint in the “Stop the Shot” case to include the NJ mandate). That suspension covered 2009, so in this new year a new annual flu vaccine requirement exists.
See: http://drrimatruthreports.com/?p=3970
Why is all this important? First, certainly, no one should ever be forced to take any vaccine against their free and informed choice. Second, the courts have created a number of obstacles to challenging FDA approval of vaccines. The Natural Solutions Foundation and its allies seek to do just that, and must align with people who are being forced, at risk of job, schooling or other value, to accept the vaccines against their free choice. That’s proven a difficult standard, since the first two sets of plaintiffs saw the mandates vanish when legal “Push Back” was initiated.
Now, however, as we respond to the recently completed Health Freedom War Council and begin the Third Round of the “Stop the Shot” litigation and as the CDC began its propaganda about a Third Wave of the so-called “pandemic” we find ourselves allied again with those whose livelihood, education or children are at risk from these uninsurable, unsafety-test vaccines.
See: http://drrimatruthreports.com/?p=4478
In the case of H1N1, the “Swine Flu” those vaccines were purchased by the US government (for $6.4 billion) then approved by the government (FDA) and then recommended by the government (CDC) and then distributed by the government (HHS). This may or may not be an unusual business model; certainly it is not worthy of respect, nor worthy of a supposed free people.
Are you finally ready to shout, “I’m as mad as hell and I won’t take it any more!”
If you are, we need your support for the “Stop the Shot” litigation. Please go to the Foundation donation page and make your most generous gift. Just end your amount in the number “6” so we can track the amounts earmarked to the case.
Donate: http://drrimatruthreports.com/?page_id=189
Ralph Fucetola JD
Natural Solutions Trustee
Countervailing Frequency Equivalents™
2017 Update:
http://drrimatruthreports.com/orpheus-project/
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January 2010 — Although the “Swine Flu” pandemic did not, and most likely will not, materialize, we thought we’d share this interesting information from Sharry Edwards MEd, since we know a number of people on the Action eAlert list are interested in frequency work.
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The Trustees of the Foundation consider Ms. Edwards’ work to be among the most advanced in the field. We are very pleased to therefore present her as a guest blogger on the Health Freedom Blog. This information has not been evaluated by the Food and Drug Administration. Not intended to prescribe for, treat, mitigate, prevent or cure any disease. –rf
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For Dr. Rima Recommends Products, Services and Information: https://www.NSFmarketplace.com
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The information contained herein, in its entirety, is under copyright, 2009 by Sharry Edwards MEd. All Rights Reserved
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Countervailing Frequency Equivalents™ for Concerns with “Pandemic Flu”
Private: for Personal Experimental Use
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It is obvious that there is a not-so-subtle ruse that attempts to eliminate a large part of the world’s population using bio-weapons disguised as vaccines . By releasing the “experimental” frequency antidotes we have found to be associated with the current swine flu, we can all be better prepared for this or any future such scheme. We strongly believe that without options, there can be no change!
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It is not my intent to trigger the wrath of any government entity, such as the FDA, which insists that only “approved” web sites can be allowed to provide or display any information relating to any resolution to the current pandemic predicted by our US health officials; but I also believe that if information is available it ought to be provided to the public. The public, so informed, is intelligent enough to make decisions based on personal observations and cognition. With the CDC now predicting a “Third Wave” of the so-called “Swine Flu” targeting older citizens this time, we all need to be alert, and very skeptical of the government’s claims.
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Individuals have a right to know about “off label” uses of health strategies. When faced with a potential pandemic it is ethical to explore every possibility. Indeed, not exploring every possibility is unconscionable.
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I should let you know that these frequencies have been used with a small population, with success, to support normal immune system response to the “Swine Flu”. Because our data base is so small, no claims can or will be made. But if there is no other choice than to submit to an oncoming pandemic, I offer the chance for people to experiment with these frequencies that we have worked for several weeks to decode. If you choose to use these frequencies, sharing your findings would benefit all of us. You use these frequencies on your own responsibility.
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These particular frequencies are the countervailing frequencies that we believe are allied with the symptom causing proteins associated with the original pneumonic plague bacterium, Yesinia pestis. The frequencies have been prepared with Rife-like devices in mind. Do not use these frequencies in a BioAcoustic device. For those of you who are BioAcoustically trained, the reasons are obvious.
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If these frequencies are a threat to any actual plan to use vaccines as a bioweapon, my life and livelihood are likely in danger. I can only guess as to what is in store for our research company. My imagination ranges from extermination to adulation. Nonetheless, we believe the public has the right to this information and the right to use it if they so choose. It is only by building a voluntary Frequency Response Team of aware individuals that we can counteract the weaponization plans aimed at us.
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We have been facilitating inquiries concerning low spectrum analogue frequency-based biomarkers and how they relate to health and wellness over the past three decades. Our work is documented in over twenty books, countless publications and more than ten documentaries. I invite you to go to www.SoundHealthOptions.com for presentations that explain much more than can this short article.
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It is our vision that once those who insist they are in control muck-up the planet to the point that it is in absolute disarray, there will be enough of us trained in this technique of frequency based energy medicine that we will be able to participate in the solutions that will begin to reestablish confidence and health to our planet.
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It is time that someone took a stand against the threat of annihilation of a large part of our world population. I provided these frequencies to the public in the hopes that such a disaster does not occur and for the reasons listed below:
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1. The information supplied to us about an impending “Swine Flu” pandemic has been incredibly conflicting even from the same agencies:
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a. The National Vaccine Information Center (NVIC) stated (October 21st 2009) that based on the US pattern of following in Australia’s footsteps concerning seasonal flu statistics, our flu season would be similar to previous years. Barbara Loe Fisher, co-founder of NVIC (National Vaccine Information Center) found no reasonable basis Obama’s (October 24th 2009) declaration of a US national health flu emergency.
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b. May 4th, 2009 (UPI) – Janet Napolitano, US Secretary of Homeland Security, stated that “swine flu was no worse than regular flu. The global swine flu threat is receding.” While another source, US Secretary of Health & Human Services, Kathleen Sibelius, is reported to have said that the swine flu could devastate the human race.
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c. An Austrian investigative journalist, Jane Burgemeister, filed criminal charges with the FBI against the World Health Organization (WHO) and the United Nations (UN) citing bioterrorism and attempts to commit mass murder. The charges involved contaminated bird flu vaccines, which Burgemeister claims she can show were deliberate attempts to cause and profit from a pandemic. Nothing is being done by any authority against Baxter, a company who admitted that they produced contaminated vaccines by “accidentally” adulterating the regular seasonal influenza vaccine with Avian Flu samples provided by WHO for experimentation. No explanation was offered as to how the sample got from one containment building to another containment building which the vaccines were manufacture. Potential Defendants include: US President Barack Obama; WHO Margaret Chan; US Secretary of Health & Human Services, Kathleen Sibelius; UN System Coordinator for Influenza, David Nabarro; US Secretary of Homeland Security, Janet Napolitano; David de Rothschild, banker; Werner Faymann, Chancellor of Austria; Alois Stoger, Austrian Health Minister and others who Burgemeister states created, and belong to, an international corporate criminal syndicate which has “developed, produced, stockpiled and employed biological weapons to eliminate the population of the US and other countries for financial and political gain.”
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Burgemeister charges that the possible defendants “conspired with each other and others to devise, fund and participate in the final phase of the implementation of a covert international bioweapons program involving the pharmaceutical companies Baxter and Novartis.”
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We don’t know who to believe but we are more apt to believe information coming from a source that has no hidden agenda; which is the case for NVIC. In the case of Burgemeister, why would anyone take such risks unless solid and obvious evidence existed?
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.2. Our national media recently released information which indicates that the people mandating and recommending the “Swine Flu” inoculations hold financial interests in the companies producing and selling the vaccines. This would strongly indicate that the flu vaccine national emergency directives were/are economically motivated.
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3. The alleged deplorable actions taken against one Professor Joseph Moshe, who it is said told a reporter that he was a microbiologist who had evidence for the States Attorney regarding tainted swine flu vaccine strains and a planned Ukrainian pandemic are unacceptable. The situation is shocking and appalling. Moshe claimed to have information showing that the vaccine produced by Baxter was actually designed as a bioweapon disguised as a vaccine. It appears he was arrested and deported before he could make the information available.
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The video recording, readily available, of his detainment seems impossible to have happened to those of us who believe we live in a free country. The events and information surrounding his “capture” are available on YouTube and many other sites. It is something you would expect to see in a totally tyrannical, oppressive dictatorship; not in our once beloved United States of America.
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I believe the information contained in the reports and videos surrounding Moshe’s capture to be true; particularly since we have received no information to the contrary. I’m reluctant to want to be a party to such treatment; yet I am a party to it if I do nothing to prevent its re-occurrence. I am ashamed that my country would treat someone this way.
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4. It has been reported that Baxter BioPharma Solutions has admitted that they made a “mistake” by sending tainted vaccine materials to 18 countries. Destiny intervened when Czech laboratory personnel decided to test the vaccine, only to find that it was lethal. Many people believe that since Baxter adheres to BS3 bio-safety levels, no such “mistake” could have been accidental! Reports about the incident claim that “such a monumental screw-up was totally impossible at that level. Many safety systems would have needed to be sabotaged; many key personnel would need to be bribed. It simply could not be done without direction from the inside.”
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5. Daily new cases have reported that people are being maimed, crippled, handicapped and killed through the forced and blanket use of this current untested vaccine. The reports of spontaneous abortions are particularly troubling. More caution, more safety, more assurances and constructive outcomes that will encourage trust and certainly more testing needs to be done. Exploiting a trusting public for financial gain is reprehensible and indefensible. I am convinced that from our future, we will look upon these events as equal appalling as sacrificing virgins for a good crop.
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6. I have evaluated the voice profiles of high ranking officials and medical authorities who are encouraging people to run out and get an unproven vaccine before they are no longer available. I am finding increasing and deepening discrepancies in what they are saying with words compared to what is being conveyed by the frequency analysis of their vocal biomarkers. This information is available to the public and can be found on our web sites.
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7. The predicted Fall Season “Swine Flu” threat is likely at an end but what about the next threat/bioweapon that will be thrust upon us? Let us stand united to rebuke “top-down” policies that are not in the best interests of the people.
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Respectfully submitted,
Sharry Edwards, MEd
Director
Institute of BioAcoustic Biology & Sound Health
sharryedwards@gmail.com
www.Jbab.org – Journal of BioAcoustic Biology
www.Vocalprofiling.com
www.nanoVoice.org
www.SoundHealthResearch.org
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The frequencies presented here are for the purposes of research and should remain in public use. The information contained herein is not intended for sale or use by any ill intentioned entity or person.
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*Frequency Equivalent™ – a numeric representation of a person, place, emotion or thing. A term of use coined by Sharry Edwards MEd for use with her work in Human BioAcoustics and Vocal Profiling.
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REFERENCES
http://www.nvic.org/NVIC-Vaccine-News/November-2009/H1N1–Fact-or-Fiction–by-Barbara-Loe-Fisher.aspx
http://www.washingtonpost.com/wp-dyn/content/article/2009/10/24/AR2009102401061.html
http://www.naturalnews.com/026503_pandemic_swine_flu_bioterrorism.html
http://portland.indymedia.org/en/2009/11/395259.shtml
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