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This long, detailed and immensely important article makes it crystal clear where the lies and distortions are about vaccines, whether they work, whether they cause chronic illnesses and whether they are safe.
Before you allow yourself or your wards, children, family, elders or others to take another vaccination, read this article. Listen to Dr. King discuss this article on the Dr. Rima Reports live (www.HealthFreedomPortal.org to join the chat and listen to the show or at www.OracleBroadcasting.com to listen to the show or in the archives at www.OracleBroadcasting.com following the broadcast on Sunday, October 3, 2010, 10 AM to 1 PM Eastern time.
Dr. King knows full well that vaccines are intentionally used to create disease and profit while they do nothing to prevent disease. Listen to him, read the article below and share this article as widely as possible.
Thanks for your activism. Yours in health and freedom,
Vaccines, Vaccination Programs and Knowing1 Misrepresentations
Paul G. King, PhD
Facility Automation Management Engineering (FAME) Systems
33A Hoffman Avenue, Lake Hiawatha, NJ 07034-1922
Before discussing the subjects in the title of this article, this commenter would be remiss if
he did not first set forth his biases and conflicts concerning the issues discussed in the sections and
paragraphs that follow this introduction.
As a scientist who understands that:
? Terms must be clearly defined,
? Statements must be supported by factual evidence and, where that evidence is not
readily available, appropriate citations thereto,
? Much of the information on vaccines and vaccination programs available in the
mainstream media and publications backed by the Establishment and its minions is
more propaganda, cant and Orwellian newspeak than sound science, and
? Vaccines or vaccination programs where the vaccine is reasonably safe and the
protection provided is either life saving (e.g., the rabies vaccines) or the prophylactic
vaccine is reasonably safe and effective in protecting almost all (i.e., >90 %) of those
vaccinated, long-lasting (i.e., protects that not less than 90 % of those vaccinated for
a period of not less than 50 years), and medically cost-effective, for example, the
measles only vaccine and vaccination program) should be supported,
this commenter must stand against: a) the misrepresentation of vaccines and vaccination programs
in any manner, and b) vaccination programs in which: i) those inoculated with the vaccine are not
protected or ii) more who are vaccinated suffer serious adverse injury from the vaccine than there
are disease cases in the population segments that are being vaccinated (e.g., the early childhood
hepatitis B vaccination program).
In addition, since the Establishment continually spews out a never-ending stream of near-
religious vaccine and vaccination apologia, this author sees no need to spend any time discussing
the inflated and often deceptive presentation of vaccines and vaccination programs as the
“salvation” of mankind – because such discussions belong in the realm of religion and not science.
With the preceding in mind, this author will now begin to address fundamental vaccine and
vaccination-program misrepresentations that stand in the way of our right to choose or decline any
prophylactic medical treatment, including any prophylactic inoculation with any vaccine or serum
as we, and not society, sees fit for ourselves and the minors and non-competent persons in our care.
1. “Vaccines Are Safe”
The first misrepresentation about vaccines and by far the worst is that, as a group (or
individually), “vaccines are the safest of medicines” or, more simplistically, “vaccines are safe”.
The factual evidence and the legislation protecting the vaccine makers, vaccine providers
Where the term “knowing” is used in the “knowingly” or “knew” sense that is defined in 21 U.S.C. § 321(bb) “The
term “knowingly” or “knew” means that a person, with respect to information – (1) has actual knowledge of the
information, or (2) acts in deliberate ignorance or reckless disregard of the truth or falsity of the information”.
and the healthcare establishment clearly exposes a different reality, which, in its most telling form,
can be found in the National Vaccine Injury Compensation Program (NVICP2; Title 42 of the
United States Code in Sections 300aa-10 through 300aa-34 [42 U.S.C. § 300aa-10 – 300aa-34]) in §
300aa-22(b)(1) which, under: a) the umbrella of “Standards of Responsibility” (§ 300aa-22.) and b)
the heading at § 300aa-22(b), “Unavoidable adverse side effects; warnings”, states:
“No vaccine manufacturer shall be liable in a civil action for damages arising from a
vaccine-related injury or death associated with the administration of a vaccine after
October 1, 1988, if the injury or death resulted from side effects that were unavoidable even
though the vaccine was properly prepared and was accompanied by proper directions and
warnings”. [Emphasis added]
If vaccines were truly safe, then there would be no need for: a) any NVICP legislation to
protect the vaccine makers or the healthcare providers from civil lawsuits for damages, or b) any “if
the injury or death resulted from side effects that were unavoidable” language to absolve vaccine
manufacturers from damages that include “vaccine-related injury or death”.
Clearly, unbiased scientists, the federal lawmakers, and the informed public know that, as a
group or, in most instances, individually, vaccines are not the safest medicines.
2. “Vaccines Are Effective”
If vaccines were truly effective, then there would be:
a. No need for any State to mandate any vaccination program for any vaccine –
everyone would be demanding inoculations for themselves and their loved ones,
b. No need for any mention of the unproven theory of “herd immunity”, which, in
reality, can only be a theory of “herd protection” because vaccines do not provide
blanket immunity (defined as lifetime [>50 year] protection from disease) to even
those who have been inoculated with the recommended vaccines from 2 to 6 or more
times, depending upon the vaccine, and
c. No need to license vaccines based on their manufacturers’ claimed levels of
“efficacy” as measured by some minimum-antibody-level surrogate for
Given the preceding factual realities, it is clear to any rational person that unqualified
phrases, like “vaccines are safe” and “vaccination programs are effective”, are simply propaganda
slogans that vaccine makers, the healthcare establishment, pro-vaccine academics, pro-vaccine US
governmental agencies (e.g., Department of Health and Human Services [DHHS], the Centers for
Disease Control and Prevention [CDC], the Food and Drug Administration [FDA], the National
Institutes of Health [NIH] and the Public Health Service [PHS], to name a few) and other vaccine
apologists continually use in their efforts to both brainwash and coerce the public into accepting
whatever vaccines and vaccination programs that “these groups” have decided, at a given point in
time, are “good” for the public as a whole with little or no regard for the fiscal or physical health of
The full title of the NVICP in the United States Code is: TITLE 42 – THE PUBLIC HEALTH AND
WELFARE, CHAPTER 6A – PUBLIC HEALTH SERVICE, SUBCHAPTER XIX – VACCINES, Part 2 –
National Vaccine Injury Compensation Program.
any individual or individuals that such vaccination programs may harm, maim or kill or, for that
matter, the fiscal and physical health of the people of the United States Of America (USA).
3. “Vaccine Panacea: The More Vaccines We Get, The Healthier We Will Be”
a. The Legacy (Pre-NVICP) Vaccination Programs
Reviewing the history of vaccines and vaccination programs in the USA, up until the early
1900s, the only widely used human prophylactic (disease-preventive) vaccine was the live-virus
cowpox vaccine, vaccina; the only other general human-use vaccine was the attenuated rabies
vaccine used to treat people who had been bitten by a rabid animal; and the only large-scale mass
“vaccination” program was the “smallpox” inoculation program.
In the 1920s, a diphtheria vaccine was introduced and its use spread; in the 1950s, the use of
pertussis vaccines became widespread but these morphed into the first combination the DTP
vaccine, which was to become the first Thimerosal-preserved combination vaccine to be used in a
mass vaccination program.
In the 1950s, the Salk inactivated-polio vaccines were introduced for mass use without
adequate testing and purity leading to: a) an initial increase in paralytic polio cases until the clinical
definition of paralytic polio was changed and b) the introduction of SV-40 and other animal viruses
which were, to varying degrees and levels, contaminants of all the polio vaccines produced for the
next three decades; and, a few years later in the early 1960s, the live-virus Sabin oral polio vaccines
displaced the Salk inactivated-polio vaccines – the Sabin oral polio vaccines were used in the USA
until 2000 when, because all paralytic polio cases were cases caused by exposure to the vaccine-
strains of the live vaccine, the US switched back to a Salk-type inactivated-virus polio vaccines,
which is still in use today.
In 1963, a live-virus measles vaccine was introduced and put into mass use shortly after its
introduction; the measles-only vaccine was followed by a measles-rubella (Merck’s measles-rubella
vaccines, MR® and MR® II, that have been discontinued); then a measles-mumps-rubella vaccine
(Merck’s MMR® vaccine); and finally an improved measles-mumps-rubella vaccine (Merck’s
MMR® II vaccine)3.
In the early 1980s, though some other vaccines were being licensed, they were not being
recommended for mass use in childhood vaccination programs because of the increasing number of
lawsuits where the parents of vaccine-injured children, principally by the DTP vaccines and the
Polio vaccines but also by the measles and MMR vaccines, were winning ever larger monetary
judgments against the vaccine companies.
Faced with decreasing profit from the lawsuits, the major vaccine makers threatened to stop
making vaccines unless the government passed legislation that protected them from most all direct
civil legal actions for the harm their vaccines caused in some of the children who were being
inoculated with these vaccines.
In addition to the combination measles-mumps-rubella vaccines (MMR® and then MMR® II), Merck continued to
make the individual component vaccines, Attenuvax®, Mumpsvac®, and Meruvax® II until the mid-2000s. In 2010,
Merck announced that, in spite of customer demand for the individual vaccines, Merck would not resume
producing these vaccines.
from the pen of Paul G. King, PhD
In late 1986, comprehensive legislation was enacted that included the National Vaccine
Injury Compensation Program (NVICP) that was codified in 42 U.S.C. §§ 300aa-10 through 300aa-
34 and, in stages, became effective in 1987 and 1988.
This legislation was originally supposed to: a) provide a speedy, “no fault”, non-litigious,
fair compensation program for vaccine-injured children and their families, which, after initial
appropriations to start the program, was to be paid for by a tax on each disease component in each
dose of vaccine administered, and b) shield the vaccine makers from being easily sued.
In return for this protection, the vaccine manufacturers were supposed to make ever-safer
vaccines that caused less adverse reactions under strict governmental oversight that would not only
compel vaccine makers to make safer vaccines but punish them when they did not make vaccines as
safe as possible and reduce the risk of adverse reactions.
In actuality, all that the NVICP has done is shield the vaccine makers from being sued and,
through an increasingly slow, litigious, convoluted, and unfairly administered “compensation
program”, its administrative hearings have only compensated a very small percentage of those who
are damaged by adverse reactions to vaccines even though the program has been expanded to
include adults in many instances.
In 1987, Congress took the first action to decrease the fairness of the program and reduce the
financial burden on the federal government and the vaccine makers for any violation by repealing §
300aa-18, which indexed the compensation for both vaccine-related death and the vaccine
manufacturers’ fines to the rate of inflation.
Next, the NVICP program administrators started making it harder for children’s families to
collect for vaccine injuries by, in the 1990s, removing many of the indications from the “Vaccine
Injury Table” (see: Sec. 300aa-14. Vaccine Injury Table) without any independent scientifically
sound justification for removing them, which forced many more cases to be heard in a proceeding
that has become increasingly litigious and unfair4.
In the late 1980s, though it was clear that the diphtheria, tetanus, acellular pertussis (DTaP)
vaccines produced a lower rate of adverse reactions in children given them than the corresponding
diphtheria, tetanus, whole-cell pertussis (DTwP) vaccine, based on the data from Japan, which
introduced the DTaP vaccine in 1981 and saw a sharp decline in both diphtheria-tetanus-pertussis-
vaccine-related adverse reactions and vaccine-related deaths, the DTwP vaccines were still licensed
and being given in the USA until 1997, when the vaccine makers finally switched to making the
This continual indication reduction process has gone beyond the absurd, removing the rotavirus vaccine indication
for intussusception even though all of the rotaviruses have been shown to cause intussusception in some vaccinated
children and two new rotaviruses (a 5-component bovine-human hybrid rotavirus vaccine [RotaTeq®] and an
attenuated human rotavirus vaccine [Rotarix®]) have been licensed and approved for mass use instead of amending
the table entry for the withdrawn RotaShield ® rhesus-monkey/human hybrid rotavirus vaccine and, most recently,
proposing to further alter the allowable time windows for the few remaining indications in the Vaccine Injury Table
(see: Federal Register / Vol. 75, No. 176 / Monday, September 13, 2010 / Proposed Rules / 55503 – 55507).
As one article correctly reports, “4) The old whole-cell version of DPT, given until about 1997 in the US, was bad. It
had a high rate of serious reactions, and these researchers calculated its effectiveness at only around 48%. But for the
previous 20 years, parents in the US were being told their children must have this vaccine. The real truth about a
After all, after 1986, the vaccine maker’s principal goad to make safer vaccines, the
monetary awards to successful plaintiffs in civil court cases seeking compensation for the injuries
caused by their vaccines, had been removed.
By comparison, the legal replacement for this goad was a weak and obviously ineffectual
federal governmental bureaucracy over which the vaccine makers obviously had significant
influence, and, given Merck’s Gardasil HPV vaccines’ problems and the federal government’s
failure to take any substantial action against the vaccine or the vaccine maker, currently have even
b. The NVICP and Post-NVICP Vaccination Programs
With the passage of the NVICP legislation, the stream of vaccines from a growing number
of vaccine makers and/or their subsidiaries has increased to a veritable river.
Discarding any semblance of a need for cost-effectiveness in any mass vaccination program,
the Establishment has moved to not only add more doses of vaccines that were already marginally
cost-effective or not even cost effective but also to propagandize vaccination programs where the
underlying vaccine is not even truly effective or, in some cases, not even reasonably safe.
In addition, the Establishment, using a hired Institute of Medicine (IOM) committee as its
surrogate, redefined the allowable “placebo” in a vaccine clinical safety trial from only a pH-
buffered sterile isotonic saline solution to include: a) the entire vaccine formulation without the
active antigens, b) some other experimental vaccine or c) some other licensed vaccine, and
convinced the regulators to look at relative incidence of adverse events instead of their absolute
incidence in determining that a given vaccine is “reasonably safe”.
Together, these changes altered the basis for “safety” in phase 3 clinical trials and, by
increasing the adverse reactions in the “placebo” group, reduced the relative level of each adverse
reaction in the candidate vaccine compared to that adverse reaction in the “placebo” group.
Thus, when “three” children in the test group for Merck’s RotaTeq® vaccine in as clinical
trial (conducted in an overall population where sanitation is poor) developed intussusception and
“one” child in the control group developed intussusception, the RotaTeq vaccine was still
approvable and approved because the rate of intussusception was not significantly higher (on a
statistical basis) than the rate in the controls because of the small size of the groups in phase 3 trial
that Merck had conducted.
On this basis, the FDA licensed Merck’s genetically engineered, bovine-human-hybridized,
pentavalent, oral, live-virus rotavirus vaccine, RotaTeq, even though this vaccine’s actual rate of
intussusception was 3 times that found in the control group.
Of course, after its approval in February of 2006, the pediatricians were told that, unlike the
previous “intussusception prone” rotavirus vaccine, Wyeth’s RotaShield®, which was withdrawn
shortly after its introduction in 1998, RotaTeq’s on-label use would not cause intussusception.
Even after being told that RotaTeq does not cause intussusception, the RotaTeq-related
intussusception signal in the voluntary Vaccine Adverse-Event Reporting System (VAERS) [where
particular vaccine being kind of dangerous and ineffective doesn’t come out until the pharmaceuticals decide they
have something better” (emphasis added). [See: http://www.exploringvaccines.com/?p=686]
typically less than 10% of actual adverse events for a given vaccine are reported] was even larger
after RotaTeq began to be used than the signal seen from the previous, now-withdrawn
“intussusception prone” RotaShield rotavirus vaccine and, in addition, RotaTeq-related cases of
Kawasaki’s disease were also reported6.
Additionally, after the NVICP was enacted, several patently unsafe or problematic vaccines
were licensed (e.g., LymeRX™ for Lyme disease and RotaShield® for rotavirus) and, after causing
horrendous or significant harm to those vaccinated with them from which the Establishment
profited, simply withdrawn from the market.
Thus, in addition to the pre-NVICP childhood vaccination programs for DTP, MMR and
Polio, we now have ineffective and/or less-than-effective vaccines and less-than-effective and/or
non-cost-effective mass vaccination programs for: a) late-childhood/adult diphtheria-pertussis-
tetanus (Tdap), b) childhood Haemophilus influenzae, type B (Hib), c) early childhood/adult
Hepatitis B (Hep B), d) childhood chickenpox, e) childhood/adult Hepatitis A (Hep A), f)
childhood/adult meningococcal meningitis (Sanofi Pasteur’s Menomune® and Menactra® vaccines),
g) Streptococcus pneumoniae (Wyeth’s Prevnar® and Prevnar ® 13[childhood] and Merck’s 23-
valent Pneumovax® [adult]), h) childhood rotavirus (Merck’s RotaTeq® and GlaxoSmithKline’s
(GSK’s Rotarix®), i) adult Shingles, and j) mid-childhood/young-adult human papilloma virus
(HPV; Merck’s Gardasil® and GSK’s Cevarix®) as well as k) ineffective annual vaccines and
annual vaccination programs for viral influenza in children and adults with “11” different vaccine
formulations currently being produced in “eight” manufacturing sites.
Moreover, not only does this require more and more vaccines to be given during childhood
but also, further unmasking the reality that vaccination is not immunization, to increase “coverage”
(in reality, market size and market penetration), adults are increasingly recommended to: a) get
“boosters” doses or “booster” vaccines, b) get periodic Tdap boosters in lieu of tetanus boosters,
and c) accept additional vaccine doses whenever there is a disease outbreak of a “vaccine
preventable” disease in their community regardless of their disease status.
In addition, no meaningful action has been taken against the vaccine makers for their failure
to expeditiously safen US vaccines by removing all preservatives and reducing the level of
adjuvants used or, where possible, eliminating the use of adjuvants altogether.
Instead, though there currently is a limit on the permitted level of aluminum adjuvant in
each vaccine7, the total level of aluminum adjuvants administered is being allowed to increase
without limit and the vaccine makers are increasingly demanding that they be permitted to use so-
called “oil-in-water” adjuvant systems even though, based on animal usage, these are known to be
more serious immune-system disruptors than the current long-used aluminum adjuvants whose
long-term safety for use in human vaccines has not been proven individually much less collectively.
Geier DA, King PG, Sykes LK, Geier MR RotaTeq vaccine adverse events and policy considerations. Med Sci
Monit. 2008 Mar; 14(3): PH9-PH16.
If the FDA’s proposed changes to 21 CFR § 610.15. Requirements for constituent material as published in the
Federal Register (see: Federal Register 2010 March 30; 75(60): 15639-15642) are adopted by the FDA, the FDA
will be able to waive all of the current limits, including those for preservatives and adjuvants as it sees fit even
though doing so is a subversion of the foundation upon which the regulation o all drugs is based – the applicable
regulations as set forth in 21 CFR Parts 600-680 are current good manufacturing practice (CGMP) minimums,
which every covered biological drug product must meet.
Finally, in spite of being sued for the failure of the Secretary of the Department of Health
and Human Services (hereinafter, the Secretary) to make vaccines safer and reduce the risk of
adverse reactions, as required by 42 U.S.C. § 300aa-27(a), by removing Thimerosal (49.55 %
mercury by weight) from the list of approved chemicals that can be used to manufacture vaccine,
the federal government has yet to ban the use of Thimerosal, a chemical that is known to induce
anaphylactic shock in some and mercury poison susceptible developing children, in the manufacture
c. The Number of Vaccine ‘Doses’ Reality
Increasingly the public is being told that they must submit to ever-expanding vaccination
programs for themselves and their children without regard for the risks to their own health or the
health of their children because complying is for the “greater good”.
For children up to 6 years of age, the recommended vaccination program reached a new high
in 2009 when, in addition to all of the 38 vaccines in the 2007 and 2008 vaccination programs, three
more doses of an 2009-A-H1N1 influenza vaccine was added for a nominal total of 41 doses of
Relative to 1983, the maximum relative level of mercury from possibly Thimerosal-
preserved vaccines (marked in red in Table 1 on the next page) was 1.6 times the nominal level of
exposure in 1983 and, roughly correcting for 10-or-more-times-larger effect of the prenatal
mercury dose, effectively up to 5-plus times the level of adverse impact relative to the vaccine
exposure to injected Thimerosal (49.55% mercury by weight) in 1983.
d. The Continuing Use of Mercury (Thimerosal, 49.55% Mercury by Weight) Reality
When it comes to the issues surrounding the serious adverse health impacts of Thimerosal
(49.55% mercury by weight) on those vaccinated with vaccines containing it, the public is
continually propagandized with one of two misleading and inaccurate slogans:
1. “Mercury has been removed from all childhood vaccines” or
2. “All vaccines given to children, except some flu vaccines, no longer contain any added
The reality is that the Establishment, faced with a growing public outcry against the use of
Thimerosal as a preservative in childhood vaccines, did gradually reduce the level of Thimerosal in
the previously Thimerosal-preserved vaccines from nominally 25 micrograms of mercury per 0.5-
mL dose to about 1 mcg of mercury per 0.5-mL dose (a reduced-Thimerosal or “trace”-Thimerosal
vaccine formulation) in the period from 2001 to 2005 and then starting in 2004, phased out the use
of Thimerosal in childhood vaccines.
However, to offset this reduction in mercury exposure from childhood vaccines (and the
serum Rho(D) products), the Establishment-controlled CDC began publishing recommendations in
April of 2002 that, during the annual flu season: a) pregnant women who would be in their second
and third trimesters and b) children 6 months to 23 months of age should get a flu shot (see
Prevention and Control of Influenza Recommendations of the Advisory Committee on
Immunization Practices [ACIP]. MMWR 2002 April 12; 51(RR03): 1-31) at a time when all FDA-
approved influenza vaccines were Thimerosal-preserved vaccines.
Table 1: The CDC-Recommended Vaccine Schedule Comparison in Children
from Conception to 6 Years of Age, By Year (Recommended Month)
Year USA 1983 USA 2007 USA 2009
Before Birth — Influenza shot
Seasonal influenza &
Birth through 1 Year DTP (2) Hep B (birth) Hep B (birth)
OPV (2) Hep B (1) Hep B (1)
DTP (4) DTaP (2) DTaP (2)
OPV (4) Hib (2) Hib (2)
DTP (6) IPV (2) IPV (2)
[5 total] PCV (2) PCV (2)
[75 mcg Hg] Rotavirus (2) Rotavirus (2)
Hep B (4) Hep B (4)
DTaP (4) DTaP (4)
Hib (4) Hib (4)
IPV (4) IPV (4)
PCV (4) PCV (4)
Rotavirus (4) Rotavirus (4)
Hep B (6) Hep B (6)
DTaP (6) DTaP (6)
Hib (6) Hib (6)
IPV (6) IPV (6)
PCV (6) PCV (6)
Influenza (6) Seasonal Influenza (6)
Rotavirus (6) 2009-A-H1N1 (6)
Influenza (7) Rotavirus (6)
 Seasonal Influenza (7)
[25; 50 mcg Hg] 2009-A-H1N1 (7)
[50; 100 mcg Hg]
1 through 2 years MMR (15) Hib (12) Hib (12)
DTP (18) MMR (12) MMR (12)
OPV (18) Varicella (12) Varicella (12)
[3; 8] PCV (12) PCV (12)
[25; 100 mcg Hg] Hep A (12) Hep A (12)
DTaP (15) DTaP (15)
Hep A (18) Hep A (18)
Influenza (18) Influenza (18)
[8; 30] [8; 33]
[12.5; 62.5 Hg] [12.5; 112.5 Hg]
2 through 3 years Influenza (30 Influenza (30
Influenza (42) Influenza (42)
[2; 32] [2; 35]
[37.5; 100 mcg Hg] [37.5; 150 mcg Hg]
4 through 6 years DTP (48) MMR (48) MMR (48)
OPV (48) DTaP (48) DTaP (48)
[2; 10] IPV (48) IPV (48)
Varicella (48-60) Varicella (48-60)
[25; 125 mcg Hg] Influenza (54) Influenza (54)
Influenza (66) Influenza (66)
[6; 38] [6; 41]
[50; 150 mcg Hg] [50; 200 mcg Hg]
Vaccines and values in a red font are for vaccines that were, in 1983, or, in the 2000s, may still
The CDC made these recommendations in spite of the fact that the flu vaccines were
“Pregnancy Category C” vaccines with no proof:
a. Of non-teratogenicity for the fetus or reproductive safety for the pregnant women;
b. That the flu vaccines were not mutagenic or carcinogenic; or
c. That the flu vaccines were in-use effective in preventing those vaccinated from
There was, as is the case today, also no proof that flu vaccines, of any kind, are more in-use
effective than a placebo injection in preventing those children under 2 years of age who are
inoculated with a flu vaccine from contracting influenza.
As: 1) the level in the childhood vaccines continued to declined, 2) some doses of “trace”-
Thimerosal flu vaccines became available, and c) a live-virus flu vaccine was introduced, the CDC
recommendations continued to try to maintain the adverse effects of the average level of mercury
exposure to Thimerosal by: a) removing the restriction as to when, during pregnancy in the flu
season, flu shots could be given; b) increasing the upper limit on children to first 35 months, then to
59 months, then to 107 months, and, finally, to 18 years of age; and c) requiring children to get two
flu shots (a month apart) the first time they were vaccinated.
In 2009, the maximum level of Thimerosal exposure was doubled in utero and at 6 months
and 7 months when the CDC: a) added the “pandemic”, “swine flu”, 2009-A-H1N1 influenza to the
vaccines recommended to be given once to pregnant women and twice to children under 9 years of
age, and b) also designated pregnant women and young children as targeted “high risk” groups.
? Most of the doses of available influenza vaccines are Thimerosal-preserved doses,
? The CDC steadfastly refuses to even express a preference for pregnant women and
young children to get “no Thimerosal” influenza vaccine doses and
? The FDA continues to illegally license Thimerosal-preserved vaccines for which the
vaccine manufacturer has never proven that the level of Thimerosal used as a
preservative in said inactivated-influenza vaccines is “sufficiently nontoxic …” as
required by the applicable portion of the current good manufacturing practice
(CGMP) safety regulations set forth in 21 CFR § 610.15(a),
pregnant women and children are continuing to be injected with toxic levels of mercury from
these adulterated drugs8
Moreover, given the CDC’s decision to increase the upper age limit for children to 18 years
and recommend that all adults be vaccinated annually, if Thimerosal-preserved flu shots continue to
be administered and some children and their mothers during pregnancy only get Thimerosal-
preserved flu shots, clearly the total dose of mercury exposure will continue to exceed the
maximum level that children born in the 1990s would have received from the three Thimerosal-
preserved childhood vaccines, DTaP, Hib, and Hep B, given to all children before 2001 and to some
Thimerosal-preserved vaccines for which the manufacturer has failed to meet the applicable clear CGMP minimum
“sufficiently nontoxic …” requirement for the vaccine dose set forth in 21 CFR § 610.15(a) are adulterated drugs
under 21 U.S.C. § 351(a)(2)(B).
from the pen of Paul G. King, PhD
children into the 2004 – 2005 timeframe, if no changes had been made to the Thimerosal-preserved
childhood vaccines or in the recommendations for the use of Thimerosal-preserved inactivated-
influenza vaccine formulations to inoculate pregnant women and developing children.
As long as the preceding realities continue to exist, any claim that there can be no link
between: a) the level of mercury exposure and b) the risk of neurodevelopmental disorders, chronic
illnesses and abnormal behaviors is obviously a specious claim because the maximum level of
mercury has not dropped from the 2000 level but rather the maximum exposure level has increased.
At the same time, the levels of neurodevelopmental disorders, chronic medical conditions,
and abnormal behaviors have not dropped but rather these levels have also collectively increased.
Based on the preceding and other key facts (e.g., the several-fold excess level of males as
compared to females in the neurodevelopmental disorders and the fact that increases in these
disorders were noticed a couple of years after the 3-dose regimens for Thimerosal-preserved Hep B
and for Hib were implemented in the late 1980s in the USA and in the 2000s after similar program
changes were implemented in New Delhi, India9), this author knows that mercury exposure from
Thimerosal in vaccines and other drugs is the major causative factor in many, if not all, of the
epidemic-level increases in neurodevelopmental disorders, chronic medical conditions, and
4. “The Benefits Outweigh The Risks”
Pointing to our current increased life expectancies and ignoring their projected future
decline, the Establishment continually tells Americans that the benefits of each new vaccination
program outweigh the risks.
Unfortunately, there has been epidemic increases in many chronic diseases (e.g., asthma in
children from < 1 in 1,000 children in the 1970s to > 1 in 10 children in the 2000s) and the
morphing of previous chronic diseases only seen in adults (e.g., type 2 diabetes) into chronic
diseases seen in children to the point that, in 2006, more than 26 % of American children have one
or more chronic diseases (up from 12.8 % in 1994)10 that they most probably will have over their
Thus, the “greater good” for whom each of us is supposed to sacrifice ourselves and our
loved ones is, in actuality, the “greater good” for one or more segments of an Establishment that
feeds on us and grows ever stronger as more of us weaken and become chronically ill and/or
financially and physically drained trying to care for our chronically ill loved ones.
Worse, there is increasing evidence that those who are effectively in control of this
Establishment decided have, unconsciously or consciously, that they need to:
The reality of this linkage was recently strongly reinforced by the emergence of a similar pattern’s being observed
in a New Delhi, India nursery school after the New Delhi pediatricians began recommending the addition of 3-
doses each Thimerosal-preserved Hib and Hep B vaccination programs to the Indian government’s recommended
Thimerosal-preserved DTP vaccination program in 2000 and the worsening of the outcomes when these programs,
originally designed to finish the 9-shot vaccination series by the time the children are 6 months of age, were
shortened to be completed by 4.5 months of age and the incidence of neurodevelopmental dysfunction doubled.
Van Cleave J, Gortmaker SL, Perrin JM. Dynamics of Obesity and Chronic Health Conditions Among Children
and Youth. JAMA 2010 February 17; 303(7): 623-630.
? Increase the harm,
? Further drain our fiscal and physical strength, and
? Reduce our numbers and our life expectancy, while feeding on our fiscal and physical
To that end, increasingly expensive vaccines (e.g., Merck’s Gardasil and GSK’s Cervarix,
where the private-sector list price for each dose is than US $125.0011) that: a) are less-and-less
curative and/or effective and b) seem to be more-and-more harmful are being approved and
delivered to the public as preventives for conditions whose incidence, in many instances, may have
been caused or aggravated by other vaccines, drugs, processed and genetically altered foods, and
chemicals that the Establishment markets to the public as “safe” without any real proofs of the
short-term and, more importantly, true long-term safety for any of these Establishment products.
To sell these less-than-effective, less-than-proven-safe, and much-more-expensive vaccines,
the Establishment continually reminds the public of the horrors of the deaths from “vaccine-
preventable disease” for certain highly contagious and lethal diseases from the era before vaccines
(e.g., smallpox, polio and measles), diseases that have disappeared (e.g., smallpox) or only occur at
low levels (e.g., measles) in the USA today, while ignoring or minimizing the following critical
? Clean water, sanitation, basic food safety, improved housing, and antibiotics did
more to reduce the level of the disease-related injuries and fatalities from the highly
contagious and lethal diseases than the vaccines for them have done,
? Without any vaccine, scarlet fever, a highly contagious and lethal disease, has
? Many of today’s vaccines are for diseases that: a) are not highly contagious (e.g.,
influenza and hepatitis B) or b) do not have any significant mortality levels (e.g.,
chickenpox, mumps, rubella, and tetanus).
? The obviously vaccine-related increases in chronic diseases, especially chronic
diseases that have a significant autoimmune component, like asthma, multiple
sclerosis, chronic fatigue syndrome, lupus, and diabetes, to name a few, as well as
epidemic increases in abnormal childhood neurodevelopment, abnormal behaviors,
other developmental abnormalities and bowel disorders.
In addition, when we were first being sold on mass vaccination programs as a means to
protect the health of the public, we were told that a mass vaccination program for any vaccine
depended on the vaccine’s being effective and the mass vaccination program’s being cost effective.
Consider the “chickenpox” vaccination program where the vaccine, Merck’s Varivax®, is a
live-virus vaccine that infects every one inoculated with it with a certain strain, the Oka/Merck
strain, of herpes varicella zoster (HVZ) – a vaccine strain that is not effective in preventing
CDC Vaccine Price List (Prices last reviewed/updated: September 24, 2010): Merck’s HPV-Quadrivalent (Types 6,
11, 16 and 18) Recombinant Vaccine, Gardasil, US$ 130.27/dose; GSK’s HPV-Bivalent (Types 16 and 18)
Recombinant Vaccine, Cervarix, $ 128.75/dose, where both process include a US$ 0.75 excise tax nominally
collected for the NVICP in 10-dose vials: $1302.70 plus shipping and handling for each Gardasil vial and $1287.50
vial. The commercial list price costs of the two 3-dose series are US$ 390.81 and US$ 386.25, respectively.
from the pen of Paul G. King, PhD
everyone vaccinated, or even all of those with a “sufficient” vaccine-strain antibody titer level, from
also being infected by the “native”/“wild” strains of HVZ circulating in the USA.
When the initial licensing for this vaccine was sought in the 1990s, the justification for
licensing a chickenpox vaccine for a normally mild and innocuous childhood disease was that
vaccination was marginally cost-effectiveness on a societal productivity-loss basis under the
presumptions that: a) one dose of vaccine would provide lifetime protection for most young
children inoculated with the vaccine and b) there would be no serious adverse reactions to being
inoculated with the vaccine.
Yet, today, two doses of Varivax® are the minimum recommended for all children, and older
adults are being recommended to receive a dose of Merck’s Zostavax®, a higher-concentration Oka-
strain HVZ vaccine to “prevent” a recurrence of the HVZ (native or vaccine-strain) with which they
have been infected.
Without even considering the costs to treat those who have severe adverse reactions to the
Varivax or Zostavax vaccines, a conservative 2009 cost analysis placed the US excess shingles’
cases’ costs, caused by the US childhood chickenpox vaccination program, at US$ 700 million
Clearly, the Establishment has discarded the requirements for vaccine effectiveness and
In their place, Establishment profitability seems to have: a) overruled the federal
government’s concern for public’s fiscal and physical health and b) trumped the significant costs
from the collective long-term vaccination-induced physical harm, including maiming and death,
that some of those who are vaccinated suffer12 when the serious adverse effects caused by the initial
vaccine, Varivax® (which was claimed to cause no serious adverse effects in the FDA-
licensing/approval process), Merck’s MMR-Varicella vaccine, ProQuad® (which has a significantly
higher risk of serious adverse effects), and Merck’s shingles HVZ vaccine, Zostavax®, are factored
Currently, the Establishment is engaged in introducing vaccines, like Merck’s Gardasil® and
GlaxoSmithKline’s Cervarix®, with no proof of long-term effectiveness and self-generated, self-
serving “cost effectiveness”, which clearly ignore the costs to those who have had, are having and
will have serious adverse reactions
Furthermore, after their approval, the CDC immediately recommended mass vaccination
programs for these vaccines with almost no in-use proof of safety and no in-use proof of
effectiveness in preventing cervical cancer.
Worse, both the CDC and the FDA seem almost total indifferent to the hundreds of reported
vaccine-induced injuries as well as the tens of vaccine-linked deaths, which, quite predictably, the
Establishment attributes to mere coincidence.
In addition, the Establishment has introduced vaccines, like the current rotavirus vaccines,
that have clearly negative US cost-effectiveness (where the cost of the vaccination program far
Tellingly, before Merck’s Gardasil® HPV vaccine was introduced, Varivax consistently had the highest incidence
of adverse-event reports in the VAERS database in the 1990s and early 2000s.
exceeds the costs of the background level of rotavirus in the USA) and, for Merck’s genetically
engineered RotaTeq®, have clearly increased US rotavirus disease risk in those children and adults
who were previously “immune” to the native human rotavirus strains to which they have been
exposed during their childhood but are not protected from being infected by the genetically
engineered bovine-human hybridized viruses in Rotateq.
Moreover, the standards for licensing a vaccine in the USA have been reduced from the
vaccine: a) must be truly effective in preventing the disease in most of those who have been
vaccinated and b) must reduce the harm from the disease in those who are vaccinated and still
contract the disease as well as c) reduce the transmission of the disease to:
? In the case of the rotavirus vaccines, for the limited and biased clinical trials
conducted, the vaccines were approved based on a finding that the risk of the serious
harm caused by the vaccines is not statistically higher than the risk of harm caused
by the natural disease in the control population used in the phase-3 clinical trials.
? In the case of the human papilloma virus (HPV) vaccines, the vaccines were
approved based on claims that the vaccines may, in this instance, prevent some
vaccine-associated cervical cancers in some of the vaccinated women three to five
decades after they complete the initial 3-dose vaccination schedule, even though:
a. There is no proof that HPV infection causes cervical cancer — only proof that
HPV infection levels are associated with cervical cancer,
b. The “efficacy” data indicates a post-vaccination loss of efficacy in less than a
c. The strains of HPV in either vaccine (HPV types 6, 11, 16, and 18 in Gardasil
and types 16 and 18) are not even the major strains of the disease prevalent in
the USA – in fact the type 11 strain is almost non-existent (“0.1%”) in the US
d. The approvals are not questioned when the levels of adverse-event reports,
including serious maiming and death, currently far exceeds the level of the
other vaccines even though only a small percentage of the eligible population is
being vaccinated with these vaccines while the level of vaccination in most of
Dunne EF, Unger ER, Sternberg M, McQuillan G, Swan DC, Patel SS, Markowitz LE. Prevalence of HPV
Infection Among Females in the United States. JAMA. 2007 February 28; 297(8): 813-819.
The most common HPV types detected were HPV-62 (3.3%; 95% CI, 2.2%-5.1%) and HPV-84 (3.3%; 95% CI, 2.2%-
5.1%), HPV-53 (2.8%; 95% CI, 2.1%-3.7%), and HPV-89 (2.4%; 95% CI, 1.4%-4.3%) and HPV-61 (2.4%; 95% CI,
1.6%-3.8%) (FIGURE 2). HPV-16 was detected in 1.5% (95% CI, 0.9%-2.6%) of females aged 14 to 59 years. There
was no statistically significant difference in the prevalence of HPV-16 and the 13 more commonly detected types, except
for HPV-84 and HPV-62. HPV-6 was detected in 1.3% (95% CI, 0.8%-2.3%), HPV-11 in 0.1% (95% CI, 0.0 %-0.3%;
relative SE_30%), and HPV-18 in 0.8% (95% CI, 0.4%-1.5%) of female participants. Most participants infected with
HPV (60.1%) had only 1 HPV type detected (95% CI, 53.2%-67.9%); however, 23.9% had 2 types (95% CI, 18.3%-
31.3%) and 16% had 3 or more types detected (95% CI, 12.0%-21.2%). Overall, HPV types 6, 11, 16, or 18 were
detected in 3.4% of the study participants, corresponding with 3.1 million females with prevalent infection with HPV
types included in the quadrivalent HPV vaccine. Few participants (0.10%) had both HPV types 16 and 18 and none had
all 4 HPV vaccine types. At least 1 of these 4 HPV types was detected in 6.2% (95% CI, 3.8%-10.3%) of females aged
14 to 19 years.”
… Our data indicate that the burden of prevalent HPV infection among women was higher than previous estimates.
However, the prevalence of HPV vaccine types was relatively low”. [Emphasis added.]
the other vaccine programs that generate significant levels of serious adverse
events generally exceed 75 % of the population segments covered by the
5. “The Establishment’s Efforts To Increase Their Protection From Civil Lawsuits Are
Furthermore, through an appeal in Bruesewitz v. Wyeth being heard by the US Supreme
Court this Fall, the vaccine makers and the rest of the Establishment are essentially attempting to
have the Supreme Court rule that the 7th Amendment14 of the Constitution of the United States of
America, an integral part of the “Bill of Rights” reserved to the people of the United States of
America, does not apply to those who have suffered, or are the guardians of those who have
suffered, a vaccine-induced injury.
The artifice being used to carry this argument is that 42 U.S.C. § 300aa-22. Standards of
responsibility is an issue that can be decided once, and for all, by the judiciary, outside of a civil
trial by jury on the facts of each case.
This argument is being advanced even though, under the NVICP, the vaccine maker’s lack
of liability under § 300aa-22 is supposed to be the issue decided in the first phase of any vaccine-
related civil jury trial.
That such liability decisions belong to the trial jury is clearly set forth in § 300aa-23. Trial,
which at § 300aa-23(b), states:
The first stage of such a civil action shall be held to determine if a vaccine
manufacturer is liable under section 300aa-22 of this title”. [Emphasis added.]
Moreover, the Establishment’s arguments knowingly ignore § 300aa-22(b) with respect
“warnings”, in general, and § 300aa-22(b)(2), which states:
“For purposes of paragraph (1), a vaccine shall be presumed to be accompanied by proper
directions and warnings if the vaccine manufacturer shows that it complied in all
material respects with all requirements under the Federal Food, Drug, and Cosmetic
Act [21 U.S.C. 301 et seq.] and section 262 of this title (including regulations issued
under such provisions) applicable to the vaccine and related to vaccine-related injury
or death for which the civil action was brought unless the plaintiff shows – …”
? As the putative causative DTP vaccine in question is a Thimerosal-preserved vaccine
given to the child and
? The vaccine manufacturers have admitted knowingly failing to comply with Title 21
of the Code of Federal Regulations (21 CFR) as set forth in section 610.15(a) (21
CFR § 610.15(a)), which requires the level of preservative must be proven to be
“In Suits at common law, where the value in controversy shall exceed twenty dollars, the right of trial by jury shall
be preserved, and no fact tried by a jury, shall be otherwise re-examined in any Court of the United States, than
according to the rules of the common law”.
“sufficiently nontoxic so that the amount present in the recommended dose of the
product will not be toxic to the recipient”, in testimony given before a Congressional
committee which investigated the vaccine makers and the US Food and Drug
Administration’ actions from 1999 and which subsequently published a formal
Congressional report, “Mercury in Medicine – Taking Unnecessary Risks” in 200315
and the requirement in question is a material requirement under the Federal Food,
Drug, and Cosmetic Act [21 U.S.C. 301 et seq.] as well as a safety regulation issued
under the provisions in “section 262 of this title”16 [emphasis added],
the Wyeth defendant is clearly guilty of failing to comply “in all material respects with all
requirements under the Federal Food, Drug, and Cosmetic Act [21 U.S.C. 301 et seq.] and section
262 of this title (including regulations issued under such provisions) applicable to the vaccine and
related to vaccine-related injury or death for which the civil action was brought”.
Moreover, recognizing defendant Wyeth’s knowing and intentional failure to comply with
the black letter law, the US Supreme Court should, when it hears the case this Fall: a) find for the
Bruesewitz plaintiffs and b) take whatever actions needed to ensure that the Bruesewitz plaintiffs
are awarded appropriate punitive damages for defendant Wyeth’s knowing and willful failure to
comply with 21 CFR § 610.15(a) for the preservative Thimerosal in the vaccine that caused the
harm to the Bruesewitz child.
However, given the Establishment’s denial of reality of vaccine-induced mercury toxicity in
susceptible children, like the Bruesewitz child, who were, and are still being, given vaccines
preserved with Thimerosal (49.55% mercury by weight) and the power that the Establishment
wields, the people will be lucky if the US Supreme Court finds for the Bruesewitz plaintiffs.
Finally, should the US Supreme Court find for Wyeth, then, the people will most assuredly
know that both the Establishment and the US Supreme Court are knowingly severing those who
bring vaccine cases against the vaccine manufacturers in the legal manner provided by NVICP from
the right to a civil jury trial for damages that is supposedly guaranteed by the 7th Amendment to the
Constitution of the USA.
6. “The ‘Life Saving’ Annual Influenza Vaccination Program”
Factually, there is no scientific proof that the influenza vaccine prevents even most (> 50%)
of those who are “vaccinated” with an influenza vaccine from contracting and spreading influenza
during the “flu season” – none whatsoever (see, for example, Geier DA, King PG, Geier MR.
Influenza Vaccine: Review of Effectiveness of the U.S. Immunization Program, and Policy
Considerations. J. Am. Physicians and Surgeons 2006 Fall; 11: 69-74 [the only US-population-
See Finding 3, “3. Manufacturers of vaccines and thimerosal, (an ethylmercury compound used in vaccines), have never
conducted adequate testing on the safety of thimerosal. The FDA has never required manufacturers to conduct adequate safety
testing on thimerosal and ethylmercury compounds” (page 6), in May 2003, Subcommittee on Human Rights &
Wellness of the Government Reform Committee, US House of Representatives (Chairman Dan Burton – following
a 3 year congressional investigation), “Mercury in Medicine – Taking Unnecessary Risks” pgs 1-80 and, in
abbreviated form, published in the Extended Congressional Record: Subcommittee on Human Rights and Wellness,
Committee on Government Reform of the House of Representatives, “Mercury in Medicine Report,” Washington,
DC, as published in the Congressional Record, pgs. E1011-E1030, May 21, 2003
Here, “this title” is “TITLE 42 – THE PUBLIC HEALTH AND WELFARE” of the United States Code.
wide retrospective of in-use effectiveness evaluation – not model – for the influenza vaccination
programs in the USA for the years 1979 through 2001]); and other unbiased independent studies as
well as the independent reviews of the published studies (see, for example: Jefferson T, Di
Pietrantonj C, Rivetti A, Bawazeer GA, Al-Ansary LA, Ferroni E. Vaccines for preventing
influenza in healthy adults. Cochrane Database of Systematic Reviews 2010, Issue 7. Art. No.:
CD001269), which clearly show that the inoculation of populations with influenza vaccines, both
inactivated- and, more recently, live-virus, is not effective in preventing those who are inoculated
from getting “influenza” during the “flu season”.
Furthermore, there is some evidence that getting an influenza inoculation in one year may
increase the inoculated individual’s risk of contracting an influenza infection in a subsequent year
Additionally, a recent double-blind clinical trial study found that supplementation with
vitamin D-3 was much more effective in preventing influenza-type-A infections than influenza
vaccination (see: Urashima M, Segawa T, Okazaki M, Kurihara M, Wada Y, Ida H. Randomized
trial of vitamin D supplementation to prevent seasonal influenza A in schoolchildren. Am J Clin
Nutr. 2010 May; 91(5): 1255-1260. Epub 2010 Mar 10. PMID: 20219962).
Finally, as is usually the case, Establishment’s fear mongering and propagandizing carefully
hides the fact that influenza is not a highly contagious disease (see: Cannell JJ, Zasloff M, Garland
CF, Scragg R, Giovannucci E. On the epidemiology of influenza. Virol J. 2008 Feb 25; 5: 29 [Note:
Among the issues this electronically published review article addresses is the absence of any valid value for the sick-to-well infectivity for human influenza in spite of numerous attempts to determine even a valid estimate, which clearly establishes that influenza is not highly infective.]).
Thus, the Establishment is recommending mandates for various groups of people, and the
State of New Jersey is currently mandating, a non-effective vaccination program for a disease that is
not highly contagious on the grounds that, to say the least, this less-than-scientifically-sound, non-
effective prophylactic treatment, influenza vaccination, will somehow protect those who submit to it
from spreading a disease that it does not prevent them from contracting, and, when those inoculated
get the live-virus vaccine, a disease with which those receiving it not only are directly infected by
three strains of live viral influenza but have also been shown to shed the live virus for at least 21
days after being inoculated with said live-virus vaccine.
Furthermore, in spite of an ever-increasing body of evidence that vitamin D-3
supplementation is a more effective preventive for type “A” influenza than any influenza vaccine,
this Establishment continues to ignoring this proven and highly effective prophylactic use of
vitamin D-3, which protects all against contracting all strains of type “A” human influenza, instead
of suboptimal protection from getting the two (2) type A strains of flu in the flu vaccine.
Obviously, the Establishment’s recommendations and actions are not grounded in sound
science nor based on public health concerns; they are clearly driven by other imperatives.
7. “Medical Mandates Are Required For The ‘Greater Good’”
Whenever this author hears any group or zealot, including any vaccine apologist,
recommending that any person should surrender his or her right to make his or her own informed
medical decisions to some “higher authority” (be it employer, state or nation) “for the greater
good”, this commenter knows that the group or person advocating for such is a medical fascist17
who is seeking to take away our personal freedom to make medical choices for ourselves and those
for whom we are responsible and who is advocating for a “religious cult”, the cult of the “public
health” vaccinationists, who seek to mandate that all must sacrifice or risk sacrificing some aspect
of their own or their children’s health on the vaccine altar “for the greater good” – the good of the
Establishment – of which the group or individual demanding the surrender of the rights to informed
choice and consent is a well-paid member, who depends on promoting these sacrifices for his or her
status, position, and/or livelihood.
8. “Vaccines, the Safest of Prophylactic Healthcare Measures”
We are repeatedly sold the myth that “vaccines are the safest disease-preventive medicines”,
when the truth is that, as a group, they are the least safe of disease-preventive medicines (see: Neil
Z. Miller’s Vaccine Safety Manual For Concerned Families and Health Practitioners, 2nd
edition (2010), ISBN 978-188121737-4) and the only class of prophylactic medicines for which
there are no long-term safety studies and, increasingly, not true-placebo-controlled short-term large-
scale safety studies (in a vaccinated versus totally unvaccinated [using sterile isotonic pH-balanced
saline for the controls] with > 50,000 in each arm of the study).
In addition, instead of proof of effectiveness and long-term (lifetime [> 50-year protection])
effectiveness, we are given antibody-titer-based measures of claimed efficacy of limited duration
(typically, 10 years or less) for “most vaccines” after typically 2 to 5 inoculations for most
(typically, > 60%) of those who are initially inoculated multiple times, with a carefully concealed
reality that each such inoculation campaign kills a few18 who are inoculated and harms some
additional multiple of that number each year to varying degrees.
9. “Vaccines Do Not Cause Autism Or Any Other Chronic Medical Condition”
How much longer will Americans tolerate the increasingly obvious lie that the
Establishment’s vaccination programs are not a causal factor in ‘Autism’ and other chronic
childhood medical conditions that once were rare (< 1 to 2 instances in every 10,000 children) but
are now at epidemic levels (> 1 instance in every 10 to 1,000 children)?
How much longer will the American public continue to tolerate the epidemics of chronic
diseases; and epidemic rates of chronic disease that, for asthma, now exceed 10 % of our children
and, in the aggregate, have brought us to a nation where, in 2006, more than 25%19 of our children
have at least one chronic lifetime medical condition so that the Establishment may continue to grow
Defined here as any member of medical community who favors dictatorial medicine where all medical decisions
are under the control of the “medical police” and “medical courts”; and the individual has no rights to make his or
her own informed medical decisions without fear of any retribution, ostracism or oppression.
Based on the reality that vaccination accounts for most of our excess infant mortality rate over that infant mortality
rate in Japan in the first year of life, this “few” deaths per vaccination collectively translates to about 2 per 1,000
live births or about 8,000 – 9,000 newborn babies in the USA each year.
“The rate of chronic health conditions among children in the United States increased from 12.8% in 1994 to 26.6%
in 2006”. [http://www.medscape.com/viewarticle/717030?sssdmh=dm1.591574&src=nldne&uac=140083MY] [Note: 26.8/12.8 is about a
factor of 2.1 – without considering the increase in population of children by about 50% – making the population
percentage increase not 210 % but rather 300+ %.]
and profit at the expense of the increasing damage to the fiscal and physical health of ourselves and
How much longer will the American public be blinded by the propaganda spewed forth
daily by these servants of greed who have been and are knowingly sacrificing our health and
prosperity so that the Establishment they serve may continue to grow in size and profit while our
fiscal and physical health is stolen from us?
Even though this commenter cannot answer for those who read these questions, his past and
on-going efforts clearly point out the reality that he has lost his tolerance for the status quo and, with
eyes wide open, he is seeking to open the eyes of the public to the preceding realities and to march
with that informed and enlightened public to change the USA, not for the “greater good”, but rather
for a return to a system of laws in which the rights of every competent citizen are respected and
everyone has the freedom to freely choose, or reject, all prophylactic vaccination programs without
any penalty, stigma, or recriminations from those who do not share the same views.
In addition, this commenter is: 1) seeking to change the laws protecting the Establishment’s
vaccine purveyors from being held directly accountable for the harm their vaccine products cause
and the lack of safety and/or appropriate effectiveness of many of their vaccine products and 2)
hoping that, after reading this commentary, those who ‘get it’ will join with this commenter in
demanding: a) direct vaccine purveyor accountability and b) the absolute right to choose which, if
any, vaccination programs and when, if ever, the vaccines chosen should be administered – or,
simply, “opt in” vaccination laws in every State, which would repeal the current mandates and
eliminate any and all need for an exemption of any type from any prophylactic or other vaccination
About Paul G. King, PhD
Paul G. King, PhD Analytical Chemist, is a scientist who has studied both vaccines and
vaccination programs intensively for more than a decade and has sorted out the underlying science
to the extent that he could find such from all of the published information available from those with
differing views about vaccination and vaccination programs.
If any, after reading this article, any reader finds any significant error for which there is
unbiased science that clearly supports your alternative views, then, by all means, send your
alternative view or views and their supporting documentation to me through email@example.com and, if
your studies are truly unbiased, this author will be glad to: a) modify his views accordingly and b)
publish an updated article. If you find areas where the text has grammatical, spelling or word-
usage errors, please let the author know so that he may appropriately correct them and published a
revised version of this article.
For additional information about Dr. King and his interests, the reader can visit his
personal web site, http://www.dr-king.com/.
MONEY BOMB! MONEY BOMB! MONEY BOMB!
Natural Solutions Foundation
The Voice of Global Health Freedom™
IT’S MONEY BOMB TIME!
To Fund Health Freedom’s Next Victory!
Health Freedom Money Bomb – Round Three!
December Annual Giving Season
TOGETHER We’ve held off the uninsurable, un-safety tested, martial law-friendly “Swine Flu” H1N1 vaccine panic… and the Senate delayed voting on the (sic) “Food Safety” bill, S.510 after nearly a hundred fifty thousand emails to the committee and Senate…
Congratulations to US! We won a couple rounds! Our Push Back and Stop the Shot law suit forced the US to effectively “cancel” the H1N1 Pandemic. Oh, there are the usual “talking head” announcements about how dangerous H1N1 still is and a bizarre National Emergency Declaration from the President that seems to contradict his own Secretary of Health, but the juice is gone: there is no serious threat either from the disease (there never was) nor, with insufficient supplies, from the vaccine (which is where all the danger really lay). Both New York and New Jersey, the only two states with flu vax mandates, suspended theirs after we went to court on one and threatened to do so on the other. But we have a long way to go before we are finished with these threats.
This Money Bomb’s continued success can be our most powerful Push Back to the President’s “National Emergency Declaration” of October 23, 2009 regarding the alleged “swine flu pandemic”. See: http://drrimatruthreports.com/?p=3763
The depopulationists / globalists / pharma-terrorists and their government/WHO/UN henchmen and henchwomen (such as Napolitano, Sebelius and Hamburg) will be back again. By the time they mount their next terror tactic, we will be stronger, even better organized and ready to beat them back on that one, and the next, and the next, all because of your help.
Round Three… [But that’s a secret; we have cooperating plaintiffs and are preparing to file.]
Oh, by they way, did you forget about Codex? We didn’t. In fact, now that Gen. Bert and Dr. Rima can safely travel without fear of deadly injections, they went to the most recent Codex Committee on Nutrition and Foods for Special Dietary Uses (CCNFSDU), whose Chairman is the notorious Dr. Rolf Grossklaus.
They attended this meeting in Dusseldorf from Nov 2-6, and all workshops and associated meetings – for you. As usual, they did daily video updates, radio specials and so on. You know you can count on them to tell you what is happening and make contacts with delegates from around the world that can change history – just as we did with the H1N1 scam-for-death-and-money.
We need you to help us generate the funds needed to move our seminal legal challenge to the entire vaccine approval travesty forward, fighting any appeal that the FDA and other defendants may initiate and we need the funds to make sure that we can continue our Codex work. We need funds to update our Codex book and make sure that every Head of State, every Minister of Health and Agriculture and every Codex delegate gets that publication along with a clear explanation of how to use this information. Despite the (ill-informed) Nay-Sayers, when Austria, Hungary and the Netherlands used our Codex Two Step Process, they won their cases in the WTO, escaping both trade sanctions AND Codex in those instances!
We need money to help reclaim the production of food here at the Valley of the Moon(TM) Eco Demonstration Project. Right now the government of Panama is asking us to help them turn ALL cattle farming in the breadbasket province of Chiriqui into BeyondOrganic/Biodynamic farming. They are asking us to help them do the same with their agricultural production, as well. We need money to support volunteers who provide hands, heads and hearts to make this project work so that we can teach farmers and non farmers alike how to grow clean, abundant food for life and health here and elsewhere.
What does that have to do with you and your health? A lot. First, we can create products which, because of their excellence, will violate Codex guidelines and standards and can then be shipped internationally, helping to further crack Codex apart. Second, we are creating a teaching center to help farmers from the developing world, where more and more of your food comes from, to grow their food in a way that is healthy for them AND for you. That means, of course, that their countries, too, will need to follow our Two Step Process to ship and sell their products.
AND we need serious funding to complete the Health Freedom Documentary which we began, but did not have enough funding to complete.
So much to do. So much to do for you. How can we do it all? Simple: we need the resources and then we can do it all – you know that you can trust the Natural Solutions Foundation to be on top of issues before they arise and find the solutions. You know you can trust us to use every single penny for the Foundation’s work since none of the Trustees takes a penny for our much-more-than-full-time work. You know that we are 100% supporter supported so that our only focus is what is good for health, and for freedom. We are there for you.
Now it is time for you to be there for Health Freedom with a powerful, decisive Money Bomb!
Lay it on us so we can keep health freedom free. Just think! Today you are free of the threat that was looming over our heads: the voluntary-but-really-mandatory adjuvanted vaccine for a made-up, make-believe disease. And we, you and the Natural Solutions Foundation, did that together. What else can we do? Let’s find out. It’s Money Bomb Time!
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News, alerts, and Other Relevant Health Freedom information
PLUS: Action Items You Need to Take Now!
Natural Solutions Foundation
The Voice of Global Health Freedom™
Health Freedom Action eAlert
August 9, 2009
Three for Liberty Campaign: We Have Three Weeks Before Congress Reconvenes!
The Natural Solutions Foundation Has Identified 3 Key Issues Impacting Our Liberty.
Here’s what you can help us accomplish:
1) Protect our right to Self-Shield – NOT be required by laws already in place to take the “swine flu” jab.
2) Reverse the FDA/FTC violation of our right to learn and share the benefits of supplements and herbs.
3) STOP the enactment of (sic) “Food Safety” bill, HR 2749, which allows the FDA to declare martial law, invade your home, degrade your food supply and forbid you to save seeds or grow clean, wholesome foods.”
Visit the Three For Liberty Campaign to Take Action on All Three Now!
* Congress is on its August Recess and you can easily visit your Congressmen and women in their home districts to explain why you want the right to self shield, rather than be forced to take a vaccine or be incarcerated
* The dangerous Swine Flu vaccine is being tested on children and pregnant women* NOT for safety, but for dosage, and has not yet been deployed on a mandatory basis
* The Senate has not yet voted on the total give-away of our food supply to the very forces that are killing us with dangerous and unsafe food, Agribiz
* Every Member of Congress can be educated about the importance of HR 3394 and 3395 in protecting both our health, our health freedom and our Constitutional right to free speech
Right now, you have an outstanding opportunity to act decisively and powerfully to speak for Liberty, and protect her – and yourself. The next three weeks, while Congress is on recess, can be the time when we, the net roots of health freedom, act in such compelling numbers that we do, indeed, protect our health and our freedom from the forces that are trying to overwhelm both of them.
* Vaccine “testing” began yesterday at St. Louis University although the FDA said on July 23, 2009 that it would approve the Swine Flu vaccine for general use BEFORE safety tests were completed – and this for a disease which is “less severe than the seasonal flu.”
Reality check: while you are being reassured that vaccination will be voluntary, two facts bear recalling:
1. As we have previously documented, in 2005 the World Health Organization gave itself the authority to dissolve sovereign governments and take control should there be a “pandemic”. That determination did not stipulate a real pandemic, any pandemic will do.
That declaration states, ” Under special pandemic plans enacted around the world including the USA, in 2005, national governments are to be dissolved in the event of a pandemic emergency and replaced by special crisis committees, which take charge of the health and security infrastructure of a country, and which are answerable to the WHO and EU in Europe and to the WHO and UN in North America.”
This suggests very strongly that the faux pandemic was orchestrated disease or no disease and therefore represents a serious threat to liberty as well as to the social order.
2. Although HHS Secretary Sibelius, Dr. Fauci, head of the National Institute of Allergy and Infectious Diseases (NIAID) and other government officials repeated on CSPAN today that there will be no forced flu vaccinations, the situation is a bit more complex: If Pandemic Emergency powers are invoked, you could be given the “choice” to accept a flu shot or not. If you do, whatever the consequences are, you can sue no one, and no one is liable for your damages (or death). If you “choose” not to accept the “voluntary” flu shot, you will very likely then be faced with incarceration/quarantine/detention.
Despite the legalism, I would call that mandatory vaccination, wouldn’t you?
You Are the Key.
You Decide to Mobilize All of Your Contacts on These Three Key Issues and We Are Unstoppable
1. Swine Flu Vaccination: Big Pharma wants you vaccinated. The US government wants you vaccinated. Baxter, Novartis, Glaxo-Smith Kline, and Sanofi Pasteur executives are members of the advisory group that on July 13th recommended mandatory H1N1 vaccination of everyone in all 194 countries that belong to the WHO.
The plans for the final globalization of the planet needs you to be vaccinated.*
You, of course, do not need to be vaccinated for a trivial disease which has been inflated into a Level 6 Pandemic by the agency which can then take command of the political power of the world.
But here in the US, you have already sent 1.3 MILLION emails to Congress, State Legislators, Governors, Secretary Sibelius of HHS, Secretary Napolitano of DHS and the White House demanding the right to self shield.
Think for a moment what actually happens if, in addition to submitting an email for each member of your family, you mobilize your circle of influence to do the same, and they spread this populist demand further still? What happens is that we get what we demand: the right to NOT take a vaccine for Swine Flu if we don’t want it AND the right not to be incarcerated if we reject the vaccine.
*”USNORTHCOM is the global synchronizer – the global coordinator – for pandemic influenza across the combatant commands” Brig. Gen. Robert Felderman, deputy director of USNORTHCOM’s Plans, Policy and Strategy Directorate: (See Gail Braymen, USNORTHCOM contributes pandemic flu contingency planning expertise to trilateral workshop, USNORTHCOM, April 14, 2008, Also see USNORTHCOM. Pandemic Influenza Chain Training (pdf) (Chossudovsky, 2009)
2. End FDA/FTC Gag Rule on Health and Food: Dr. Ron Paul has given us two new bills that go to the heart of the FDA/FTC violation of our right to learn, and to share, what benefits food components like supplements and herbs can give us.
These bills need to be supported by asking your members of Congress to become co-sponsors and return our Constitutional Rights to us.
3. Prevent Total Industrialization of US Food Supply: The House has passed HR 2749, which allows the corrupt and deadly FDA to declare martial law, invade your home, degrade your food supply and forbid you to save seeds or grow clean, wholesome foods.
We know these outcomes are important to you. The Natural Solutions Foundation has prepared 3 helpful Resource Documents at http://drrimatruthreports.com/?p=3241to serve as talking point papers when you visit your Congressmen and women during the recess, to share with those whom you are mobilizing, to serve as information points for letters to the editor, to share with the people who shop in your health food store, etc.
Resources for the
Three For Liberty Campaign
Liberty Needs Us Now:
Protect Against FDA / FTC, Food Fascism, First Amendment Violations and Swine Flu Vaccines
Share These Three Health Store Leaflets for Three Weeks to Save Health Freedom
As Mark Twain is alleged to have opined, “No Man’s Life Liberty or Property is Safe…While the Legislature is in Session” – and certainly no person’s health freedom and food freedom are safe either. Well, Congress is not in session at the moment, and we have about three weeks to educate our representatives while they are home. And as you may have noticed in the media, they are hearing these freedom truths from their constituents!
Please attend any “town hall meetings” held by your representatives and let them know that your personal health freedom is as important an issue the “health care” debate, which is really mostly about who will pay for conventional medical treatment, and how will it be rationed. To the contrary, we’re concerned about Natural Solutions, so we need to concentrate on protecting people from toxic drugs (including vaccines) and from toxic foods as well. Our agenda is not the same as the agenda being portrayed on the mass media. The 3 Leaflets have bullet point information for you to use in educating your representatives about our Health Freedom Agenda.
Thus, the focus of our Three for Liberty Campaign, http://drrimatruthreports.com/?p=3209, our Three Weeks Campaign, needs to be educating decision makers, but also educating the concerned public – people who “get it” and understand that Health Freedom is Our First Freedom and people who CAN “get it” if you help them in that process. Therefore, we invite you to help us, by printing the three Health Food Store Leaflets attached to this blog entry and posting them at your local health food store, food co-op or similar commercial or public venue and posting them. Please print and copy as many as you can. Please re-post them on the Internet. We need to make these posters GO VIRAL!
Introduction to This Issue
Three Actions; Three Weeks
Follow the Action on Twitter
Threats to Freedom: Pandemic Panic
Our Three For Liberty Campaign,
http://drrimatruthreports.com/?p=3209, is designed to make it easy for you to act quickly and easily on the biggest threats to your liberty and your health. Take the action steps we’ve set up for each of these issues!
And print the health food store / community center leaflets we’ve set up, copy and post them widely!
Gag Rule on Swine Flu options is a perfect example of FDA violation of our rights. I am not allowed to tell you that Nano silver, Vitamin C, MSM, and other immune boosters and enhances are good for dealing with Swine Flu and coming out the other side of it, quite literally.
You probably know that the FDA currently literally forbids telling you truthfully that anything other than vaccines and Tamiflu or Relenza can “treat” the Swine flu. That type of gag regulation is exactly what Ron Paul’s two bills are designed to eliminate. But until they do, all I can do is tell you that IF I could exercise my First Amendment rights as a free American, I would tell you about the fantastic effectiveness and safety record of nano silver and colloidal silver in dealing with all pathogens.
Meanwhile, it is clear that the forces arrayed against our health freedom will not rest until they either destroy those freedoms or we win this enormous war.
Of course you know where you can obtain the same Silver Solution we use, and help the Foundation at the same time:
I would also like to ask for your continuing generous elp: please make your tax deductible donation, http://drrimatruthreports.com/?page_id=189, now to help keep us keeping on in the battle for health and freedom. You need us and we need you. It is a marriage of support and respect. Thanks!
Natural Solutions Foundation
Weaponized Vaccination Prepared for Phony Pandemic…
The URL for this article is: http://drrimatruthreports.com/?p=2802
URGENT ACTION ITEM: Demand the right to self-quarantine (self-shield) instead of vaccination or involuntary quarantine NOW. Tell State and Federal officials and legislators that you want to make your own health choices in the event of a pandemic declaration. Click here (http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27275) NOW and then share this article with everyone on your list urging them to do the same.
There is no time to lose. With this coming Fall, and the promised Swine Flu Pandemic nearly upon us, and with WHO on the verge of declaring the non-lethal, bio-engineered, weaponized H1N1 Swine Flu a “Level 6 Pandemic”, for which they actually redefined “Pandemic” as “Widespread, spreading from human to human but not particularly dangerous” from its previous definition of “widespread, rapidly spreading and very dangerous”, we are very close to a marriage of the illness care system’s deadly vaccine hoax and the phony “terrorism protection” of the emerging police state in the US. What is planned, and has been legislated into existence, is the total eradication of your right to choose what does – and what does not – go into your body in the form of a mandated vaccine for a weaponized virus (which is fizzling into a non-event disease, by the way, unless resurrected by a weaponized vaccine…). The implications of this action are potentially lethal to you and any remaining vestiges of constitutionality or personal health freedom. Of course, the designation of this “disease” as a “Pandemic” would be merely laughable if the implications of a medically-induced police state were not so horrific.
Legislation is already in place which would require you to either submit to vaccination once a Pandemic State is declared by either the Secretary of Health and Human Services, the Governor of your State or both. Refuse this vaccine and you will find yourself confined either as a felon without benefit of judge or jury if the offense is a State level one, or involuntarily incarcerated in Federal FEMA holding camps if the offense is a Federal one. Either way, unless we demand, and obtain, the right to self quarantine (self-shield) once the “Pandemic” is rolled out, our only choice, if we are in the US, entering or leaving the US at that time, will be to either submit to a weaponized substance being injected into our bodies or involuntary detention for alleged (and totally irrational) “public health” purposes.
This excellent article by Stephen Lendman, Research Associate of the Centre for Research on Globalization makes many of the points that the Natural Solutions Foundation has been making for the last several years: the US government is aiding and abetting a along-term and well-orchestrated health assault on its people in the form of dangerous, uninsurable vaccinations. Their dangers are legion but, despite the propaganda to the contrary, not one of them has ever been proven safe or effective. They have all been proven wildly profitable, however both at the primary level (what the drug companies receive when they sell them to doctors, governments, military systems, etc.), secondary level (payment to the doctor’s office or health care system for administration of these toxic and ineffective injections) and at the wildly profitable third level (on-going treatment for diseases induced by the impact of both the vaccine’s active materials and the astoundingly toxic adjuvants, preservatives and other compounds included in the vaccine shot).
The list of vaccine related conditions and diseases far exceeds just the tragedy of vaccine induced autism. It extends to – and beyond –
~Leukemia (once rare, but now a common disease in both children and adults) because of the leukemia virus contamination known and tolerated for decades by the FDA
~Neurological damage (for example, epilepsy caused by the totally unnecessary Rotovirus vaccination recently added to the CDC’s Advisory Committee on Immunization Practices (ACIP), whose recommendations are increasingly being mandated by State governments and “Autism Spectrum Disorders”, Hyperactivity, Learning Disabilities and “Juvenile ALS”, a brand new disorder invented to explain why girls and women are dying after Gardasil vaccination “against” HPV)
~Asthma and pneumonia
~Genital Warts and Herpes following vaccination with Gardasil and shingles vaccines
~Guillian Barre Syndrome (post vaccination polio by another, hastily-invented name)
~Alzheimer’s Disease and Dementia (five times as likely in persons who have been vaccinated “against” flu)
~Lupus, Rheumatoid Arthritis, Multiple Sclerosis and other life-threatening auto-immune diseases
~The disease against which the vaccination was supposedly given (for example, Yellow Fever vaccine causes Yellow Fever in a significant number of people who receive it. That number increases greatly if the person is over 60 years old. Vaccine FDA-approved inserts carry the notice that the symptoms of the disease being vaccinated against are among the side effects of the vaccination!)
~Death — thousands and thousands of deaths. In fact, one might call vaccination part of the “Josef Mengele School of Medicine” and this sick joke would be frighteningly accurate.
The Natural Solutions Foundation has petitioned the Federal Trade Commission to require it to prohibit all advertising which states or implies that vaccines are either safe, effective or both, since neither is true of any vaccine: none has ever been proven safe or effective. Vaccines are, in fact, so dangerous that they are a totally uninsurable risk. Parents have received over $2 Billion from the special US Masters Vaccine Court although most cases are never heard and few are parents win their cases in this kangaroo court system. That money, of course, was not provided by the drug companies, but rather from a special tax parents (or other providers) are required to pay on every vaccine shot.
Vaccines are most profitable, however, when large numbers of doses are administered. If you want to make a lot of money, and then go on making a lot more money AND render a population infertile, vaccines are your tool.
Please take this situation seriously. Although the “disease” is not serious, the loss of freedom and imposition of a death machine is very, very serious. And please, take a moment to make a recurring tax deductible donation, large or small, to the Natural Solutions Foundation by clicking here (http://drrimatruthreports.com/?page_id=189). We are here for you. Even in difficult economic times, a dollar a month from everyone on our list will make it possible for your health freedom to have a massive and resonant voice.
First, let me congratulate you on your excellent article on preparing the US population for mandatory vaccination. As the Medical Director of the Natural Solutions Foundation, www.HealthFreedomUSA.org and www.GlobalHealthFreedom.org, I have been sounding the same alarms that you write about here in articles, blogs, blasts and radio shows.
The Natural Solutions Foundation’s primary list is approximately 1/4 million people and our materials are forwarded widely. We focus on the right to access information, natural and organic products, clean food (which most emphatically does NOT include genetically modified ones) and the right to make health choices employing these options and eschewing others, such as vaccination, if that is what people wish.
The Natural Solutions Foundation has published extensively on the dangers of vaccines and the fact that the entire science of virology stands on junk science and that political motivations, not scientific or health-based ones, control both regulation and public health policy with absolutely disastrous results.
The legislative and regulatory climate of the US, EU and, through Codex Alimentarius (the world food code), which is largely dominated and driven by multinational corporate interests – and worse – is of extreme concern to any person who is even dimly aware of the realities. In addition to the legislation you cite as posing a real threat to both freedom and health through the unchecked declaration of a public health threat or “pandemic”, I would add that PATRIOT I, II and II as well as BARDA restate, reinforce and repeat the government’s “right” to require mandatory vaccination or “treatment” for a declared health threat without substantiation, documentation, consultation or verification.
The Natural Solutions Foundation has created a call for the right to self-quarantine instead of accepting mandatory vaccination or other unwelcome treatments. We ask people to demand the right to self quarantine at
Clicking on this link allows people to send emails to their federal and state legislators, Secretary of Health and Human Services, the White House and And the Governor of their State with a single mouse click. We would appreciate it if you would let your contacts know about this option and direct them to this link.
FDA’s rush to approve vaccines and medications which provide profit, but pose significant dangers (HPV, with its genetically modified components, toxins including Polysorbate 80, a compound known to be related to infertility, stands as an outstanding example while the demonstrably lethal Sanofi-Aventis Avian Flu vaccine, now stockpiled by the US and the epilepsy and pneumonia inducing rotovirus vaccine recently added to the ACIP schedule stand as three of many) continues unabated while governments seek to offer it yet more money to degrade our health and our food through both mandatory vaccination and Codex-imposed under nutrition.
It is interesting to note that Codex Alimentarius, created at the behest of the post WWII pharmaceutical industry (once its leaders got out of jail following their sentences by the Nuremberg Commission for their crimes against humanity) is front and center in the push to remove food, and thus health, freedom and choice from Americans through the Codex-compliant agricultural bills now before Congress. We call this process “HARMonization.”
I would like to share your excellent article with our readership (with full citation, of course) and would like to invite you to be my guest on our Internet Radio Station, www.HealthFreedomRadio.com. You would be interviewed by the Trustees of the Foundation, Major General Albert N. Stubblebine III (US Army, Ret.), Ralph Fucetola, JD, and myself. Interviews are generally an hour long, but, since we are on internet radio, may run longer if our guest has more to say than fits into a rigid time frame. I suspect that you have more to say!
In your excellent article you state that the Emergency Medical Powers Act has not yet been passed by States. I must take exception to that, although I wish it were true. As of April 15, 2006, 32 states have introduced 92 legislative bills or resolutions that are based upon or feature provisions related to the articles or sections of the act. Of these bills, 37 had passed by that date. There can be little doubt that the number has increased since then.
Again, please accept my appreciation for your outstanding synthesis of these issues. I look forward to interviewing you so our listeners and supporters will have the chance to learn more about these issues.
Yours in health and freedom,
Rima E. Laibow, MD
Natural Solutions Foundation
And here is the article itself:
Readying Americans for Dangerous, Mandatory Vaccinations
Copyright by Stephen Lendman, Research Associate of the Centre for Research on Globalization
Global Research, June 10, 2009
At least three US federal laws should concern all Americans and suggest what may be coming – mandatory vaccinations for hyped, non-existant threats, like H1N1 (Swine Flu). Vaccines and drugs like Tamiflu endanger human health but are hugely profitable to drug company manufacturers.
The Project BioShield Act of 2004 (S. 15) became law on July 21, 2004 “to provide protections and countermeasures against chemical, radiological, or nuclear agents that may be used in a terrorist attack against the United States by giving the National Institutes of Health contracting flexibility, infrastructure improvements, and expediting the scientific peer review process, and streamlining the Food and Drug Administration approval process of countermeasures.”
In other words, the FDA may now recklessly approve inadequately tested, potentially dangerous vaccines and other drugs if ever the Secretaries of Health and Human Services (HHS) or Defense (DOD) declare a national emergency, whether or not one exists and regardless of whether treatments available are safe and effective. Around $6 billion or more will be spent to develop, produce, and stockpile vaccines and other drugs to counteract claimed bioterror agents.
The Public Readiness and Emergency Preparedness (PREP) Act slipped under the radar when George Bush signed it into law as part of the 2006 Defense Appropriations Act (HR 2863). It lets the HHS Secretary declare any disease an epidemic or national emergency requiring mandatory vaccinations. Nothing in the Act lists criteria that warrant a threat. Also potential penalties aren’t specified for those who balk, but very likely they’d include quarantine and possible fines.
The HHS web site also says the Secretary may “issue a declaration….that provides immunity from tort liability (except for willful misconduct) for claims of loss caused, arising out of, relating to, or resulting from administration or use of (vaccine or other pharmaceutical) countermeasures to diseases, threats and conditions determined by the Secretary to constitute a present, or credible risk of a future public health emergency….”
The industry-run US Food and Drug Administration (FDA) notoriously rushes inadequately tested drugs to market, putting their efficacy and safety into question, and turning those who use them into lab rats. It includes everyone if a mass vaccination is ordered on the mere claim of a public emergency – no proof required.
The Pandemic and All-Hazards Preparedness Act (S. 3678) is the other worrisome law, effective December 19, 2006. It amended “the Public Health Service Act with respect to public health security and all-hazards preparedness and response, and for other purposes.” Even its supporters worry about issues of privacy, liability, and putting profits over public health. Critics express greater concerns about dangerous remedies for exaggerated or non-existant threats as well as mass hysteria created for political purposes.
At least one other measure is also worrisome – The Model State Emergency Health Powers Act (MSEHPA). So far it’s just a proposal by the Center for Law and the Public’s Health – “A Collaborative at Johns Hopkins and Georgetown Universities (as) a primary, international, national, state, and local resource on public health law (and) policy for public health practitioners, judges, academics, policymakers, and others.”
MSEHPA is now “track(ing) legal responses to the emerging international response to the 2009 H1N1 (swine flu) outbreak, including declarations of public health emergency at the international, national, state, and local levels….” even though forensic evidence can’t confirm any H1N1 deaths. No emergency exists anywhere, and reporting one is all hype to sell dangerous drugs to unsuspecting people globally.
On its web site, the ACLU says this about MSEHPA:
It’s “written in a way that doesn’t adequately protect citizens against the misuse of the tremendous powers that it would grant in an emergency. (It’s) replete with civil liberties problems. Its three top flaws are that:
(1) It fails to include basic checks and balances (by) grant(ing) extraordinary emergency powers (that) should never go unchecked. (It) could have serious consequences for individuals’ freedom, privacy, and equality.”
(2) “It goes well beyond bioterrorism (with) an overbroad definition of ‘public health emergency” that may be anything a local or national authority declares for any reason with no conclusive evidence for proof.
(3) “It lacks privacy protections (and) undercut(s) existing protections for sensitive medical information.”
MSEHPA worries other organizations besides the ACLU, both conservative and progressive – including the Free Congress Foundation, American Legislative Exchange Council, conservative association of state legislators, Human Rights Campaign, and Health Privacy Project.
The Real Threat of Dangerous, Mandatory Vaccinations
In the wake of the hyped Swine Flu scare, media reports suggest mass vaccinations are coming. The May 6 Kimberly Kindy – Ceci Connolly Washington Post one, for example, headlined “US May Add Shots for Swine Flu to Fall Regimen” without saying they’ll be mandatory but reading between the lines suggests the possibility this year or later.
The writers report that “The Obama administration is considering an unprecedented fall vaccination campaign” to include regular and Swine Flu shots, the latter because it’s “spreading across the globe.”
HHS’ Dr. Robin Robinson said “We are moving forward with making a vaccine,” and if the government proceeds with a national program, enough supply will be produced to provide two doses for all Americans with spokespersons like National Institute of Allergy and Infectious Diseases, Anthony Fauci, claiming adverse reactions aren’t to be expected and adding another shot for Swine Flu “should not present a problem.”
The New York Times also hypes the scare with reports of city schools closed after unconfirmed Swine Flu cases, a few adult deaths blamed on H1N1 bringing the claimed total in the city to seven, and the World Health Organization (WHO) saying on June 3 that it’s moving closer to declaring a worldwide (Level 6) Swine Flu pandemic – even though none exists.
With all the hype, misinformation, and willful lies WHO’s Dr. Keiji Fukuda, in charge of flu, said only 117 deaths globally have been “blamed” on Swine Flu and any warning may include the caveat that the virus isn’t very lethal. A more accurate statement would explain that no forensic evidence links any deaths to H1N1, and influenza annually kills about 30,000 people in America alone – something the major media never report or that scattered accounts of any type flu deaths worldwide are no cause for alarm or reason for scary headlines.
It’s also unconscionable for the WHO, US and other nations’ officials to spread lies, deception, and hysteria so major pharmaceutical companies can foist dangerous vaccines and other drugs on unsuspecting people, harming their health and making them vulnerable to later diseases and possible early deaths.
Massachusetts May Be A Forerunner of What’s to Come
On April 28, the Massachusetts Senate unanimously passed a pandemic flu preparation bill that rises to the level of martial law. If approved by the House and signed into law, it will mandate among other measures:
— “vaccination, treatment, examination, or testing of” all individuals involved in providing health care – as perhaps step one before ordering the same process for all state residents;
— owners or occupiers of all premises “to permit entry into and investigation of the premises;”
— closure, evacuation, and decontamination of all suspected facilities; and
— restricting or prohibiting “assemblages of persons.”
Other states may be planning similar measures as precursors to mandatory nationwide vaccinations and overall suspension of civil liberty protections.
Adverse Vaccination Effects on Gulf War Troops
Before deploying to the Persian Gulf in 1990 – 91 (and thereafter to the present), all US troops got a standard series of inoculations against infectious diseases – the same ones given to all US citizens traveling to the region. After arriving, 150,000 also got anthrax vaccinations and 8000 botulinum toxoid ones even though concerns were raised about adverse long-term health consequences.
A National Academy of Sciences’ Institute of Medicine (IOM) study was conducted to assess them with results released in September 2000. In December 1997, the Department of Defense (DOD) announced that all US military forces would receive anthrax vaccinations. The Anthrax Vaccine Immunization Program (AVIP) began in March 1998 even though IOM found little published peer-reviewed scientific information on its safety.
In its study, IOM reported evidence of an association between vaccinations studied and transient acute common health effects, including redness, swelling, and fever commonly associated with other vaccinations. However, conclusive proof of long-term problems wasn’t determined – likely because study findings were skewed not to find them. More on that below.
IOM also studied botulinum toxoid vaccines and found evidence of an association between the vaccine and transient acute local and systemic effects similar to anthrax vaccinations. Again, conclusive proof of long-term adverse health effects wasn’t found – another very dubious conclusion as evidence below explains.
Military personnel usually get multiple vaccinations. IOM studied their effects but didn’t prove or disprove any long-term adverse effects. However several independent studies of British Gulf War veterans found some link between multiple vaccinations and later health problems.
Gary Matsumoto is a New York-based award-winning investigative journalist. His 2004 book, “Vaccine A: The Covert Government Experiment That’s Killing Our Soldiers and Why GIs are Only the First Victims” took sharp issue with IOM results and the Pentagon’s denial of Gulf War syndrome.
Investigating the shadowy vaccination development world, he discovered US military-employed doctors and scientists conducted secret medical experiments on US citizens in violation of the Nuremberg Code and fundamental medical ethics.
For its part, Nuremberg established legal medical experimental standards now incorporated into ethical medical codes, including:
— requiring voluntary consent of human subjects without coercion, fraud, deceit, and with full disclosure of known risks;
— experiments should avoid “all unnecessary physical and mental suffering and injury;”
— experiments should never be conducted if there’s “an a priori reason to believe death or disabling injury will occur;”
— risk “should never exceed that determined by the humanitarian importance of the problem to be solved..;” and
— experiments should be terminated if there’s reason to believe they’ll cause “injury, disability, or death to the experimental subject.”
According to Matsumoto, the Pentagon violated these and other standards, betrayed the troops, and the fundamental duty of military and civilian leaders to protect them. Since at least 1987, biowarfare development trumped the welfare of tens of thousands of GIs used as human guinea pigs for inoculation with experimental unlicensed anthrax vaccines containing squalene – an oil-based adjuvant (to enhance immunity) known for decades to cause severe autoimmune diseases in lab animals, yet administered involuntarily without disclosure of its harmful effects to human health. Matsumoto wrote:
“The unethical experiments detailed in this book are ongoing, with little prospect of being self-limiting because they have been shielded from scrutiny and public accountability by national security concerns.” He suggested the “writing (was) on the wall” of what’s to come with prospects now it may be soon.
“When UCLA Medical School’s Michael Whitehouse and Frances Beck injected squalene combined with other materials into rats and guinea pigs back in the 1970s, few oils were more effective at causing the animal versions of arthritis and multiple sclerosis.” In 1999, immunologist Dr. Johnny Lorentzen at Sweden’s Karolinska Institute found that on injection, an “otherwise benign molecule like squalene can stimulate a self-destructive immune response,” even though it occurs naturally in the body.
Other research shows that squalene is the experimental anthrax vaccine ingredient that caused devastating autoimmune diseases and deaths for many Gulf War veterans from the US, UK, and Australia, yet it continues in use today and for new vaccines development in labs. There’s a “close match between the squalene-induced diseases in animals and those observed in humans injected with this oil: rheumatoid arthritis, multiple sclerosis and systemic lupus erythematosus.”
Other autoimmune diseases are also linked to humans injected with squalene. “There are now data in more than two dozen peer-reviewed scientific papers, from ten different laboratories in the US, Europe, Asia and Australia, documenting that squalene-based adjuvants can induce autoimmune diseases in animals…observed in mice, rats, guinea pigs and rabbits. Sweden’s Karolinska Institute has demonstrated that squalene alone can induce the animal version of rheumatoid arthritis. The Polish Academy of Sciences has shown that in animals, squalene alone can produce catastrophic injury to the nervous system and the brain. The University of Florida Medical School has shown that in animals, squalene alone can induce production of antibodies specifically associated with systemic lupus erythematosus.”
Micropaleontologist Dr. Viera Scheibner conducted research into the adverse effects of adjuvants in vaccines and wrote:
Squalene “contributed to the cascade of reactions called “Gulf War syndrome. (GIs developed) arthritis, fibromyalgia, lymphadenopathy, rashes, photosensitive rashes, malar rashes, chronic fatigue, chronic headaches, abnormal body hair loss, non-healing skin lesions, aphthous ulcers, dizziness, weakness, memory loss, seizures, mood changes, neuropsychiatric problems, anti-thyroid effects, anaemia, elevated ESR (erythrocyte sedimentation rate), systemic lupus erythematosus, multiple sclerosis, ALS, Raynaud’s phenomenon, Sjorgren’s syndrome, chronic diarrhea, night sweats and low-grade fever.”
Matsumoto’s book includes numerous case studies of GIs afflicted with one or more of the above syndromes, their devastating effects, and the outlandish US government reaction – failing to acknowledge their existence or a connection between them and administered vaccines. Also denying the effects of other toxic Gulf theater exposures (like depleted uranium) as well as withholding meaningful treatments or protocols.
US Army Captain George L. Skypeck spoke eloquently for many when he said:
“Was the character of my valor less intense than those at Lexington? Was the pain of my wounds any less severe than those at Normandy? And was my loneliness any less sorrowful than those at Inchon? Then why am I forgotten amongst those remembered as ‘heros?’ ”
If mass vaccinations are ordered, millions of Americans may ask: Why do you keep using unsafe vaccines and other drugs when clear evidence shows their dangers? Why do you jeopardize all Americans by unleashing a future plague of serious illnesses, diseases, and disabilities? Why have you willfully and maliciously ruined my health?
Immunologist Dr. Pamela Asa first recognized autoimmune diseases showing up in GIs that mirrored those in lab animals injected with oil formulated squalene adjuvants. By 1997, hundreds of millions of dollars had been spent testing vaccines containing them, in animal studies since 1988 and human clinical trials since 1991 – by leading research institutes like NIH, the National Cancer Institute, and the National Institutes of Allergy and Infectious Diseases (NIAID).
According to Matsumoto, today, “Squalene adjuvants are a key ingredient in a whole new generation of vaccines intended for mass immunization around the globe” even though researchers at Tulane Medical School and the Walter Reed Army Institute of Research proved “that the immune system responds specifically to the squalene molecule.”
The immune system “see(s) and recognizes it as an oil molecule native to the body. Squalene is not just a molecule found in a knee or elbow – it is found throughout the nervous system and the brain.” When injected in the body, the immune system attacks it as an enemy to be eliminated. Eating and digesting squalene isn’t a problem. But injecting it “galvanize(s) the immune system into attacking it, which can produce self-destructive cross reactions against the same molecule in the places where it occurs naturally in the body – and where it is critical to the health of the nervous system.”
Once self-destruction begins, it doesn’t stop as the body keeps making the molecule that the immune system is trained to attack and destroy.
Immunologist Dr. Bonnie Dunbar also did extensive research on hepatitis B-inflicted illnesses and found similar autoimmune processes involved in molecular mimicry in people with devastating neuroimmune syndromes after getting vaccine injections.
Matsumoto says “Squalene is a kind of trigger for (a) real biological weapon,” what Soviet researchers called “a biological time bomb!!” and Matsumoto says is “the immune system.” When its “full repertoire of cells and antibodies (attack) tissues they are supposed to protect, the results can be catastrophic.” He and Dr. Pam Asa conclude that “Oil adjuvants are the most insidious chemical weapon ever devised,” including ones with squalene – something the Soviets knew could be used as a weapon in the 1980s.
Matsumoto says that “the real problem with using squalene (isn’t) that it mimics a molecule found in the body; it is the same molecule. So what American scientists conceived as a vaccine booster (or what’s now being developed in labs) was another ‘nano-bomb,’ instigating chronic, unpredictable and debilitating disease. When the NIH….argued that squalene would be safe because it is native to the body, just the opposite was true,” and, of course, still is. “Squalene’s natural presence in the body made it one of the most dangerous molecules ever injected into man” and using it in vaccines is outlandish and criminal.
So why does Washington sanction its use? According to Matsumoto: “scientists in the United States are now literally invested in squalene. Army scientists who developed the second generation anthrax vaccine have reputations to protect and licensing fees to reap (as well as) worldwide rights to develop and commercialize the new recombinant vaccine for anthrax” and ones for other health threats.
Disturbingly, “Many of the cutting-edge vaccines currently in development by the NIH and its corporate partners contain squalene in one formulation or another. There is squalene in the prototype recombinant vaccines for HIV, malaria, herpes, influenza (including the swine strain), cytomegalovirus and human papillomavirus.” Some of these “are intended for mass immunization(s) around the globe” and that possibility should terrify everyone enough to refuse any mandate or doctor’s prescription to take them.
Another problem is that “Autoimmunity (takes) years to diagnose” because early symptoms (headaches, joint pain, etc.) are so vague they can easily be from other causes.
From inception, vaccines have always been dangerous enough for some experts to call them biological weapons undermining health, manipulating and crippling the immune system, and creating the possibility of future debilitating diseases. So Big Pharma’s solution is new, more potent genetically engineered vaccines and drugs that may end up harming or killing many who take them, especially people with weakened immune systems.
Matsumoto and others sounded the alarm to alert everyone to avoid these poisons masquerading as protective drugs. In fact, they benefit only the bottom lines of companies that manufacture them and scientists reaping generous royalties.
Click here (http://drrimatruthreports.com/?p=2698) to read the Natural Solutions Foundation’s suggestions for safe and effective self-quarantine in case you are actually either infected with something that might make you sick or presented with the choice of vaccination or self-quarantine.
Bear in mind, however, that the genetically engineered, weaponized Swine Flu might, as of today, according to the CDC currently be infecting as many as 100,000 Americans. What kind of pandemic is that? An organism which is infecting hundreds of thousands of people who have no symptoms, virtually no deaths (and no reason to believe that those deaths ascribed to the organism are, in fact, associated with it) is not something to vaccinate against. In order to even halfway justify calling these events a “Pandemic”, the World Health Organization changed the meaning of “Pandemic” from a widespread communicable disease condition to which people have no previous immunity and which causes widespread disease and death to, well, uh, er, a disease which is transmitted from one person to another in more than two regions of the globe but without necessary disease consequences of any significance. But which may come back more unpleasantly this fall, JUST when we have a new vaccine ready which people will be forced to take so they can be protected against a disease which just about nobody dies from and which has never been shown to be a health threat of any major consequence anywhere in the world.
In fact, to make it clear just how little credibility the CDC, WHO and vaccine mafia actually have, it is worth remembering what the MMD, the Media of Mass Deception, appears to have totally forgotten: dying from Swine Flu may actually be good for your health if you are Mexican because of the 168 people confirmed dead of H1N1 Swine Flu by the US CDC, 152 of them came back to life in a miracle of biblical proportions.
Clearly, the rush to vaccinate, and to create a “Pandemic” is a political and economic one, not based on any public health threat whatsoever.
I believe that the real danger from this weaponized agent is the possibly lethal impact of the vaccine which will be presented to you and those you are responsible for along with the political danger of loss of liberty in the mad rush to “safety” from this non-pandemic pandemic. The other danger, of course, is what will happen to people who are quarantined in internment camps and what will happen to people who live through the events which will inevitably surround the creation of a phony “Pandemic” with all its attendant militarization and abusive controls.
This outstanding article which follows by William Engdahl makes a number of important points. The rush to mandatory vaccination Swine Flu, in the UK, France, Massachusetts, NY and elsewhere for Swine Flu, a disease which may not even exist (read on!), is madness.
Vaccines are extremely dangerous. No insurance company in the world will insure against the risks inherent in vaccination and they are, in fact, characterized as uninsurable risks which a special US fund (paid for by vaccine recipients) has paid out over 2billion dollars from to parents of children killed or maimed by vaccinations. The vast majority of vaccine damage are never compensated. The US Government has removed all potential liability from vaccine manufacturers making them totally invulnerable to legal repercussions for the dangerous and often deadly products they produce and sell at enormous profits.
In fact, vaccines are explicitly acknowledged not to protect against the diseases they supposedly are designed to prevent (read the Package Inserts for vaccines, available on line and in your doctors’ offices if you doubt that) and often to result in the very disease to which they are supposed to make you immune.
Vaccines are,however immensely, enormously and hideously profitable, however and so the Pharmaceutical Cartel, with virtually limitless amounts of money to bribe legislators and regulators (pretty inexpensive, all in all) and buy science (moderately expensive), public opinion (about 4 billion dollars a year) has bought for itself and its deadly products a respectability it does not deserve for products which should, in a rational society, be banned forever.
Vaccines are not automatically either safe or effective. In fact, they have never been scientifically found to be either safe OR effective. For that reason, the Natural Solutions Foundation has submitted a Citizens Petition (a law suit against the Government) to the Federal Trade Commission to compel them to prohibit advertising across state lines or via other channels which they control which suggests or implies that vaccines and their components have been found to be safe, effective or both.
Public health is, as William Engdahl points out, being militarized. But the Natural Solutions Foundation believes that forced vaccination, like forced drugging, is both wrong-headed and enormously dangerous. We therefore ask you to join us in urging decision-makers to rescind their dangerous, potentially lethal, rush to compulsory vaccination and involuntary quarantine for those who refuse vaccination with the far saner, safer and infinitely more freedom-saving
option of self quarantine. Instead of being forcibly detained for an indefinite period, self-quarantine allows you to protect yourself while staying at home, eating foods you have stockpiled for such an eventuality in your own surroundings, able to communicate with friends, family, etc.
Lawmakers in the US have already decided that in the event of a pandemic like the one that the World Health Organization says it is about to declare for the absurd and possibly non-existent “H1N1 Swine Flu” that you will be required to take whatever vaccine they throw at you or face incarceration under both the Emergency Medical Powers Acts passed by virtually every State AND the Patriot Acts I, II and II plus BARDA at the Federal Level.
The Natural Solutions Foundation believes that self quarantine, also known as “self-shielding”, is a much better, safer and well-regarded method for protecting both groups of people and individuals which you should have the right to select if you do not wish to be either vaccinated or incarcerated. We therefore urge you to take the following action step to inform decision makers and legislators of your strong desire to be permitted to use self-quarantine strategies by clicking Here (http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27275).
This novel option is both logical and time tested in other epidemic situations. The Natural Solutions Foundation is once again providing innovative solutions to the serious problems facing us around our health and our health freedom. Please take a moment to click here (http://drrimatruthreports.com/?page_id=189) to set up a recurring tax deductible donation to help keep the Natural Solutions Foundation active and working for you.
We appreciate our freedoms and appreciate your help in making it possible for the Natural Solutions Foundation to keep on keeping health freedom alive.
Sarkozy’s Secret Plan for Mandatory Swine Flu Vaccination
F. William Engdahl, Global Research
June 3, 2009
The French Government is developing secret plans to impose mandatory vaccination of the entire French population, allegedly against possible Swine Flu disease according to reports leaked in a French newspaper. The plan is without precedent and even defies recommended public health advice. Pharmaceutical giants benefit from the move, as the Swine Flu increases the trend to militarization of public health and use of needless population panic to advance the agenda.
The Sarkozy government has authorized spending of an estimated €1 billion to buy vaccines allegedly to combat or protect against H1N1 Swine Flu virus.
According to a report in the May 30 edition of the French newspaper, Le Journal du Dimanche, the Sarkozy government has authorized spending of an estimated €1 billion to buy vaccines allegedly to combat or protect against H1N1 Swine Flu virus. The only problem is that to date neither the WHO nor the US Government’s Center for Diseases Control (CDC) have succeeded to isolate, photograph with an electron microscope and chemically classify the H1N1 Influenza A virus. There is no scientifically published evidence that French virologists have done so either. To mandate drugs for a putative disease that has not even been characterized is dubious to say the least.
Even more bizarre is the admission by the US Government’s Food & Drug Administration, an agency responsible for health and safety of its citizens, that the ‘test’ is approved for premature release to test for H1N1 is not even a proven test. More to the point, there is no forensic evidence in any of the deaths reported to date that has been presented that proves scientifically that any single death being attributed to H1N1 Swine Flu virus was indeed caused by such a virus. European epidemiologists believe the deaths reported to date are ‘coincidental’ or what are called opportunistic infections.
What we know conclusively is that the people who died often had prior respiratory complications of an undisclosed nature. People die every day with respiratory diseases. In the USA alone some 36,000 flu-related deaths are recorded yearly with no undue panic or alarm. Most are elderly or patients with lung diseases. To date in all France, 24 people have been identified by health authorities as even having ‘symptoms’ of H1N1. It is worth noting that the WHO and CDC list the symptoms of H1N1: temperature, coughing, headache, runny nose. Hmmmmm. Do you know anyone with such Swine Flu symptoms? Also worth noting is that in the counting of the more than 15,000 ‘confirmed’ H1N1 Swine Flu cases worldwide the vast majority made miraculous recovery within three to seven days, just as in the case of a bad cold.
The goal: Militarization of Public Health
Increasingly it is becoming clear that the successive waves of mass panic created in recent years by CDC, WHO and leading government agencies has an ulterior motive. We have been hit with mass panic over eating beef when cattle in the UK and elsewhere developed fatal illness that was called BSE or ‘Mad Cow’ disease. Later evidence emerged that BSE was the result of vaccination of the cows to kill harmless insects that got under the animal’s skin. More recently, after reports of incidence of what is called ‘Blue Tongue’ disease in cows, sheep and goats in Belgium and Holland in 2006, animal veterinary authorities in Germany, Switzerland and Austria imposed mandatory vaccination or treatment with drugs allegedly to protect the animals from bites by insects allegedly carrying the usually harmless illness.
The vaccinations of the animal herds has been made mandatory for an illness that typically was so mild as to go unnoticed and in only extreme rare cases could be tied to death. All animals after three months must be vaccinated. The vaccines, according to a report in the Swiss publication Aegis-Impuls from 2008, resulted in mass deaths, decreased birth rates, decline in milk yields, heart attack and other severe effects. The vaccines were used despite the fact none apparently had been previously certified as safe. They typically contained aluminium hydroxide and Thiomersol or mercury, as adjuvants and or preservatives, both highly toxic and both also used in most human vaccines.
Despite mass protests and reports to the veterinary authorities in Germany, Switzerland and Austria, the warnings went unheeded and mandatory mass vaccinations continued. Little wonder that farmers are taking their tractors to the streets to protest.
The report of a secret French government plan to vaccinate every French citizen over three months of age, over 100 million doses, is more than alarming. According to the French Le Journal du Dimanche, anticipating a probable return of the virus in the fall, the government will spend nearly a billion euros to buy vaccines. Authorities will announce in the fall if they decide to make the vaccine mandatory. “We will be ready to go in a very short time”, explains the Minister of Health. According to sources, the state wants to order 100 million doses of flu vaccine from three laboratories, GlaxoSmithKline, Sanofi and Novartis. The latter two are French companies.
The French report comes just after the State of Massachusetts State Senate passed a mandatory vaccination bill that authorizes mandatory vaccination against purported H1N1 Swine Flu. In New York State the state hospital planning authority is debating making mandatory annual vaccination against flu of all public health employees, despite the fact that no approved vaccine for H1N1 exists. More and more it is beginning to appear that the scare about pandemic from flying birds or flying pigs is an excuse to justify mandatory vaccination with substances whose harmful side effects are demonstrably worse than any flu they should guard us against.
Novavax, a US pharmaceutical company based in Rockville, Maryland, conveniently enough just announced it is developing a vaccine for H1N1 based on “virus-like particles” that contain three key proteins of the flu virus without the genes required for replication. The vaccine is produced by techniques of genetic modification of organisms or GMO. The announcement came within days of the company announcing losses for the fiscal year of $36 million.
The drug Tamiflu which is officially recommended by the WHO as treatment to ‘ameliorate’ the symptoms of possible Swine Flu or H1N1 Influenza A as it has been renamed, is itself highly toxic. Health Canada informed Canadians of international reports of hallucinations and abnormal behavior, including self harm, in patients taking the antiviral drug Tamiflu. In some cases death was the result and severe lung complications are widely reported associated with Tamiflu, the drug whose main financial benefactor is believed to be its largest stockholder, former Defense Secretary Donald Rumsfeld.
In 1976 in the US President Gerald Ford, nervous about winning a close election ordered mass immunization of the population in the face of a possible pandemic to show voters he was a ‘hands on’ President. The 1976 pandemic never came but a vast number of people suffered serious neurological side effects from the vaccine that was rushed into production, including 25 reported deaths from Guillain-Barré syndrome.
Mandatory vaccination with drugs whose side effects are unknown because they have not been rigorously and independently tested begins to smack of the kind of inhuman mass human experiments carried out in the United States with mentally retarded, prisoners and other disadvantaged people or in Germany during the 1930’s.
URL to article: http://www.infowars.com/sarkozys-secret-plan-for-mandatory-swine-flu-vaccination/