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TAKE ACTION NOW! HOLD VAXOCRATS RESPONSIBLE FOR VACCINE HARM! NO FORCED VACCINES! http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=5708m
Dr. Rima’s Dispatches from the Vaccine Wars:
Vaxocrats know the deal: Vaccines are neither safe nor effective, as they must be under the laws governing them in the US. That makes, according to my understanding, EVERY vaccine used in the US an illegal, improperly registered and approved drug. What’s new here is that the unreliability of the DPT vaccine has been confirmed by the CDC itself. … read the whole article below.
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October 3, 2010
Permalink: http://drrimatruthreports.com/?p=6903
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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,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Vaccines, Vaccination Programs and Knowing1 Misrepresentations
Paul G. King, PhD
Facility Automation Management Engineering (FAME) Systems
33A Hoffman Avenue, Lake Hiawatha, NJ 07034-1922
Introduction
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
1
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
effectiveness.
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
2
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.
3
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.
3
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
DTaP vaccine5.
4
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).
5
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
greater influence.
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.
6
Geier DA, King PG, Sykes LK, Geier MR RotaTeq vaccine adverse events and policy considerations. Med Sci
Monit. 2008 Mar; 14(3): PH9-PH16.
7
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
of vaccines.
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
vaccines.
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
mercury”.
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
[25mcg Hg]
Seasonal influenza &
2009-A-H1N1 shots
[50mcg Hg]
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)
[22] Seasonal Influenza (7)
[25; 50 mcg Hg] 2009-A-H1N1 (7)
[25]
[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
be, Thimerosal-preserved.
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
contracting influenza.
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.
Since:
? 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
8
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).
9
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
abnormal behaviors.
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
lifetime.
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:
9
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.
[See: http://dr-king.com/docs/100711_ParallelsinNewDelhiIndia_AnEpidemic_b.pdf.]
10
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
strength.
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
realities:
? 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
virtually disappeared
? 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
11
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.
11
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
annually.
Clearly, the Establishment has discarded the requirements for vaccine effectiveness and
vaccination-program cost-effectiveness.
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
in.
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
12
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
decade,
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
women13, and
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
13
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.
“RESULTS
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.”
“CONCLUSION
… 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
vaccines.
5. “The Establishment’s Efforts To Increase Their Protection From Civil Lawsuits Are
Appropriate”
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:
“(b) Liability
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 – …”
[Emphasis added.]
Since:
? 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
14
“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-
15
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
16
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
(http://www.ageofautism.com/2010/05/with-flu-season-over-canada-shows-flu-vaccinations-to-be-
worse-than-worthless-.html).
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
17
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.
18
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.
19
“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+ %.]
18
and profit at the expense of the increasing damage to the fiscal and physical health of ourselves and
our children?
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
mandate.
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 dr-king@gti.net 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/.
Natural Solutions Foundation
The Voice of Global Health Freedom™
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
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Set up your recurring Tax Deductible Donation Now: http://drrimatruthreports.com/?page_id=189
Psychiatry’s 3D Shame: Deceive, Diagnose, Drug
Cassandra, the daughter of King Priam and Queen Hecuba of Troy was cursed by Apollo, whom she offended, with always being right but never being believed. She warned her father not to open the gates to the Trojan Horse but no one listened. The horse was brought in and, the story goes, in the dead of night, its huge belly was opened and the warriors hidden within destroyed Troy. Being right did not make Cassandra happy.
Being right does not make me happy when I am writing about things like deceiving, diagnosing and drugging an entire population for the benefits of anyone but the patient.
Being right when I wrote, decades ago, that the use of psychiatric drugs, especially in children, was a disastrous, brain-damaging and insane social and medical policy. These drugs are untested, toxic and will create a society of pharmaceutically damaged people rather than ill people being well treated. Being right when I said that the Diagnostic and Statistical Manuals for Psychiatry were dangerous and would lead to the expansion of diagnoses and treatment to the point where there were none who dared resist and non who were not diagnosed. Being right when I wrote that Psychiatric diagnoses rested in marketing, not in science and that treating CFL (corporate financial lust) was fundamentally insane, but that the insanity did not lie with the patient.
And being right when I wrote that possible drugging would inevitably become mandated drugging, although neither the science or the treatments were any better.
Alas, like Cassandra, my predictions did not ring real when I wrote them but we have arrived where I saw us collectively headed. Dangerous drugs for everything that even smacks of real life and universal mandating just around the corner – if we turn that corner.
First, an admission: I am, by training, a Psychiatrist, encouraged by that training to treat children, adolescents and adults. But I was, I believe, saved from violating the basic ethical standard of medicine (and, with decency, every activity which involves any of us): Primum non nocere – Latin for “First Do No Harm”.
It is my considered belief, after considerable study, clinical practice and observation, that it is literally impossible to BE a practicing Psychiatrist, FOLLOWING THE PRACTICE GUIDELINES AND “STANDARD OF CARE IN THE COMMUNITY” PRACTICES, and NOT do harm, first, middle and last. That is why I have never treated anyone for anything using medication with two exceptions: a wildly psychotic 19 year old patient of mine in a State Hospital locked ward was suffering the torments of the damned (which is what he believed himself to be) as he unendingly hallucinated his inner terror. I prescribed for him enough sedation to allow him to stop screaming after 9 days of 24 hour nightmare. I was a First Year Resident at the time and knew nothing of orthomolecular psychiatry (the use of nutrients for mental relief and health), but I knew that I had to do something to help this young man by allowing him to reach into our world and us to reach into his. Once the madness-fear-madness cycle was broken, our work began. Ironically, my Chief Resident had just returned from a sojourn with the British Psychiatrist R. E. Liang, who saw schizophrenia as a glorious adventure so I had to go toe to toe with my superior and his superior and HIS superior to provide some respite for my young patient. I did and I won that battle.
Today, neither my Chief Resident, the well-known Dr. James Gordon, nor I would medicate that patient, both of us for very different reasons.
The other patient was a lady who had been addicted to Xanax(R) by her General Practitioner. I had to write a prescription for a small amount to complete weaning her from that intentionally highly addictive, and therefore highly profitable, psychoactive drug.
That takes care of my prescription history for psychiatric drugs over a 40 year career practicing medicine and psychiatry with some of the most seriously ill patients in the world. Successfully. Very Successfully.
So you can see that the article below chills me to the bone. It announces another step down the path of subservient lunacy for the disgraced profession of Psychiatry, a profession devoted to poisoning a specific target organ in the face of better, safer, cheaper, kinder and more effective options like nutrition and NeuroBioFeedback, appropriate therapies and social and health supports.
It is my considered view after 40 years of practice, that there is no place, that’s right, no place whatsoever, for psychiatric drugs. None. But, then, it is also my considered opinion that there is no place for any drugs in the Doctor’s office, although there is a place for them in the Emergency Room or ambulance while a patient is being transported there.
Psychiatrists no longer learn to talk to, and therefore, to listen to people. They are trained to look for flags that trigger this drug being prescribed or that one. The “literature” in their journals is mostly junk, paid for, authored by, and owned by the drug companies. But then, the “scientific journals” that publish them are, in reality, little more than advertising circulars for their magnificent, deceptive and callously dishonest advertisements. Just ask Marcia Angel, who resigned in protest as Editor of the [supposedly] prestigious New England Journal of Medicine because of the deep, dark and deadly corruption of the “peer review” system and the staggering lies upon which drug studies, and therefore prescription practices, rest.
In the Reuters article below you will see a future emerging in which there are no normals any more. Normal means having problems and problems are given names which suggest drug treatments. Suggest? Did I say suggest? Today, for most of us, most of the time, it is a suggestion. But it is a MUCH better business model if the suggestion is rhetorical and the requirement is absolute. More drugs sold. More side effects. More drugs added to the regimen. More side effects. More brain damage which looks exactly like the condition for which the drugs were given in the first place.
If this reminds you of the influenza shot for “protection” which turns out to be the CAUSE of the influenza “epidemic” each year which then leads to more calls for more vaccines “against” the influenza “epidemic” and drugs to “treat” what was induced by the shots: flu, cancer, autism, ALS, infertility, diabetes, etc., etc., etc., then you are paying attention. The business model is identical.
And just as the flu shot is transitioning from voluntary to mandatory, so the use of psychoactive drugs, all of them, for “diseases” and “conditions” that any decent human being would be ashamed to label another person with, let alone “treat” them for, will soon be mandatory unless we collectively say “NO!”, as we did to the Swine Flu vaccination (now included in this year’s dangerous seasonal flu shot.
Here’s you bit: Help support the Stop the Shot lawsuit against the FDA. Now that H1N1 vaccine will be added to the seasonal flu shot, the women who lost their babies after they took it are especially important plaintiffs in this case. Click here, http://drrimatruthreports.com/?page_id=189, to set up your recurring tax deductible donation, large or small. Act now, before the Diagnostic and Statistical Manual declares caring about your life and your body a mental disorder, as caring about a healthy diet and clean food has become. There are, by the way, two names for this “disorder”:
1. “Orthorexia| from “Ortho” meaning correct and “orexis” meaning appetite
2. Complete, total and unmitigated garbage.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Valley of the Moon™ Eco Demonstration Project
www.NaturalSolutionsFoundation.org
www.InternationalDecadeofNutrition.org
Valley of the Moon Coffee
www.ValleyoftheMoonCoffee.org
NSF Virtual Malls
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
The Dr. Rima Network: www.DrRima.net
Food Freedom eJournal
www.FoodFreedomeJournal.org
Mental health experts ask: Will anyone be normal?
(Reuters) – An updated edition of a mental health bible for doctors may include diagnoses for “disorders” such as toddler tantrums and binge eating, experts say, and could mean that soon no-one will be classed as normal.
Leading mental health experts gave a briefing on Tuesday to warn that a new edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM), which is being revised now for publication in 2013, could devalue the seriousness of mental illness and label almost everyone as having some kind of disorder.
Citing examples of new additions like “mild anxiety depression,” “psychosis risk syndrome,” and “temper dysregulation disorder,” they said many people previously seen as perfectly healthy could in future be told they are ill.
“It’s leaking into normality. It is shrinking the pool of what is normal to a puddle,” said Til Wykes of the Institute of Psychiatry at Kings College London.
The DSM is published by the American Psychiatric Association (APA) and contains descriptions, symptoms, and other criteria for diagnosing mental disorders. It is seen as the global diagnostic bible for the field of mental health medicine.
The criteria are designed to provide clear definitions for professionals who treat patients with mental disorders, and for researchers and pharmaceutical drug companies seeking to develop new ways of treating them.
Wykes and colleagues Felicity Callard, also of Kings’ Institute of Psychiatry, and Nick Craddock of Cardiff University’s department of psychological medicine and neurology, said many in the psychiatric community are worried that the further the guidelines are expanded, the more likely it will become that nobody will be classed as normal any more.
“Technically, with the classification of so many new disorders, we will all have disorders,” they said in a joint statement. “This may lead to the belief that many more of us ‘need’ drugs to treat our ‘conditions’ — (and) many of these drugs will have unpleasant or dangerous side effects.”
The scientists said “psychosis risk syndrome” diagnosis was particularly worrying, since it could falsely label young people who may only have a small risk of developing an illness.
“It’s a bit like telling 10 people with a common cold that they are “at risk for pneumonia syndrome” when only one is likely to get the disorder,” Wykes told the briefing.
The American Psychiatric Association did not immediately respond to a request for comment.
The scientists gave examples from the previous revision to the DSM, which was called DSM 4 and included broader diagnoses and categories for attention deficit hyperactivity disorder (ADHD), autism and childhood bipolar disorders.
This, they said, had “contributed to three false epidemics” of these conditions, particularly in the United States.
“During the last decade, how many doctors were harangued by worried parents into giving drugs like Ritalin to children who didn’t really need it?,” their statement asked.
Millions of people across the world, many of them children, take ADHD drugs including Novartis’ Ritalin, which is known generically as methylphenidate, and similar drugs such as Shire Plc’s Adderall and Vyvanse. In the United States alone, sales of these drugs was about $4.8 billion in 2008.
Wykes and Callard published a comment in The Journal of Mental Health expressing their concern about the upcoming DSM revision and highlighting another 10 or more papers in the same journal from other scientists who were also worried. DSM 5 is due to be published in May 2013.
(Editing by Peter Graff)
http://www.reuters.com/article/idUSTRE66Q4BJ20100727
Natural Solutions Foundation
The Voice of Global Health Freedom™
www.HealthFreedomUSA.org – www.GlobalHealthFreedom.org
Wednesday, July 1, 2010
Permalink: http://drrimatruthreports.com/?p=5793
In This Issue:
Find Out About Our Next Guest on the Dr. Rima Reports
Four Blog Links You MUST Click!
On the Road to Codex
Current ‘Must Take’ Action Items
Dr.Rima Recommends
GOOD NEWS! THE NATURAL SOLUTIONS NEW MARKETPLACE HAS RE-OPENED!
Check It Out! www.Organics4U.org and www.NaturalSolutionsMarketPlace.org
A Great Way to Support Your Health and Your Health Freedom at the Same Time!
http://www.healthfreedomusa.org/store/cart.php
Don’t Forget to Order Your Valley of the Moon Coffee Now. Supplies Are LIMITED!
www.ValleyoftheMoonCoffee.org
Listen to the Dr Rima Reports
Sunday Night Starting 9 PM Eastern to Midnight…
www.BlogTalkRadio.com/FreedomizerRadio
1. 9 PM: Dr. Rima and Co-Host Ralph Fuectola address this week’s health freedom news and rumors — We’ll discuss the heath freedom information and sort out the disinformation for you…including
What to Expect from the Codex Meeting in Geneva…
2. 9:15 PM to 11 PM Eastern Time: Dr. Rima interviews Nancy Orlen Weber, healer extraordinary! Nancy will talk with us about the exceptionally gentle and powerful
Raindrop® Technique and share her stories as a successful psychic detective.
Interested in aromatherapy? Visit
http://www.drrima.net/#aroma
3. 11 PM to Midnight Eastern Time: The DR. Is IN! Dr. Rima takes your health and health freedom questions. Ask your questions by
a. Email to Dr.Laibow@gmail.com (“QUESTION” as the subject line, please)
b. Chat (join chat community at www.BlogTalkRadio.com/FreedomizerRadio)
c. Phone using our call in number, 347.324.3704
Please get as many people as you can to join our chat room since potential supporters monitor the number of people in the chat room. The more, the better!
Details & Listening Instructions here:
http://drrimatruthreports.com/?p=4850
Four Blog Links YOU MUST CLICK On and Read!
Please read and forward as widely as you can!
Petrochemical Detox Information – If the Gulf Disaster is Making You Ill, You MUST READ This and Pass It Along!
http://drrimatruthreports.com/?p=5783
How to Create a Food Supply 101: Valley of the Moon™ Moves Forward!
http://drrimatruthreports.com/?p=5745
Are YOU Making a Difference?
http://drrimatruthreports.com/?p=5746
Attention Rotary Clubs! Before You Help Distribute Polio Vaccines, CDC Says Polio Vaccine Causes Polio!
http://drrimatruthreports.com/?p=5729
On the Road to Codex
Codex Commission Meets in Geneva July 5-9
If You Want Us to Be Your Eyes and Ears At This Meeting, Make Your Recurring Tax Deduction Here, Now
http://drrimatruthreports.com/?page_id=189
US OUT OF CODEX? Dr. Rima Thinks We Should Get Out
Watch the Video
http://www.youtube.com/watch?v=AfCni-LuR_c
What Do You Think? Take the Survey
http://salsa.democracyinaction.org/o/568/t/1128/questionnaire.jsp?questionnaire_KEY=1042
Current Action Items
Each of These Action Items is Vitally Important. Please Take Once For EACH MEMBER of your Family, Then Forward to Your Whole Contact List
Include a brief note saying this is important to you and you are sure that it will be to the other person and urge them to take action and forward widely
* President Obama: Allow Natural Solutions!
* Food & Health Freedom Action Items and Video…
* Support Health Freedom of Speech Acts!
* Demand Congress Investigate Autism and Environmental Toxins!
* Stop the Fake Food and Vitamin “Safety” Bill -S.510
* Oppose “Ear Candle” Ban!
* Health Keepers Oath
Dr. Rima Recommends:
The Dr. Rima Network
www.DrRima.net
THE DR. RIMA INSTITUTE
The Valley of the Moon™ Eco Demonstration Project’s Natural Solutions Institute, which we call the “Dr. Rima Institute” for short, is about to open in the beautiful, bountiful, temperate highlands community of Volcan, Panama on August 7-8, 2010 and you are invited!
You can read more about this long-awaited opening, follow our progress (we will be posting photos and videos!) at the Dr. Rima Network web site:
where you will also find a description of many of the natural protocols to be offered at the Institute and products we love
_________________________________________________
Valley of the Moon™ BeyondOrganic Coffee
Supplies are Limited for this Artisenal, Hand Picked and Roasted Coffee. Place your gift orders now for yourself and friends.
Valley of the Moon™ Coffee make a wonderful corporate gift for friends, colleagues and clients. Gifts say a lot about the giver. Your impeccable taste is revealed when you give GMO-Free, Toxin-Free, Non Toxic Valley of the Moon™ Coffee This Year!
www.ValleyoftheMoonCoffee.org
Valley of the Moon™ Coffee: http://www.ValleyoftheMoonCoffee.org
I Promise You:
You Have Never Had a Better Cup of Coffee!
Non Toxic, Clean, Beyond Organic… Powerfully Antioxidant…
Order Yours Now!
Every Bag Valley of the Moon Coffee Supports your Physical Health and supports the Natural Solutions Foundation at the same time!
www.ValleyoftheMoonCoffee.org
What? You’re Still Drinking Ordinary Chemical Coffee?
You Have No Idea What You Are Missing!
Health Freedom’s Own Coffee, Valley of the Moon Coffee, Will Delight You, While You Support the Natural Solutions Foundation With Your Morning Java! Make a donation and get your coffee. Once you taste this exceptional brew, we know you will love it! Write to us at dr.laibow@gmail.com to let us know your experience drinking Valley of the Moon Coffee. We are confident that it will the finest cup of coffee you have ever tasted in your life, bar none!
www.ValleyoftheMoonCoffee.org
_________________________________________
Cognitive Enhancement Nutrition:
Empower Your Mind!
Dr. Rima and Gen. Bert love these leading-edge products…
Control your own mind! Feed your brain what it needs for discernment and acuity…
“These are the times that try men’s souls…” Are you ready?
Dr. Rima has designed a third, very special
Dietary Supplement Mind Enhancement Pack!
To learn more, or to try the products, go to:
Cognitive Enhancement
“News & Specials” list the three Dr. Rima Packs
For more Details about the Packs:
http://drrimatruthreports.com/?p=4558
You know there is a battle going on for your mind (or maybe against it!). Part of the Globalist Agenda to reduce human population and restrict our freedoms goes on in our own heads, as we are subjected to a level of propaganda that can only be termed “mind controlling.” Its success depends on making sure that we are dumb, dull, deluded and distracted….
See the video interview with Dr. Rima and Gen. Bert
http://www.youtube.com/v/_FL3SKYVEwE
Let me quote General Bert, “‘Focus and clarity’ were the words Ralph used to describe the Cognitive Enhancement nutrients, and that is exactly what I experienced. Both my long and short term memory are enhanced by these products and my thinking processes are noticeably sharper. I am very impressed and intend to continue using them.”
There are numerous smart nutrients, but few of them, working synergistically, have the capability of doing what these products actually do. In this battle to take back our food, our health and our freedoms, we must all be as mentally sharp as possible. That is why the genocidal elitists want us under-nourished and unable to think. I was so impressed with these products that I immediately began to study them and their impact. I researched the ingredients and am satisfied that there is no indication of a lack safety when used as directed. That’s when I decided to create combination packs that would support mental function without agitating; would enhance cognition without later let-down. Dr. Rima
If you’ve had problems placing orders for these extraordinary nutrients, we’ve set up a special email address for you to use; just email your contact information and we’ll have you called back right away!
brians@biologicsnutra.com
Natural Solutions Foundation has no corporate sponsorship. YOU are our only sponsors, but the goods and services come from companies who believe in what we are doing. Every sale helps to support the Foundation and move our health freedom actions forward. We urge you to patronize these mission-driven malls where you will find outstanding ways to support and be supported as free men and women!
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
The Dr. Rima Institute
www.DrRima.net
Valley of the Moon™ Eco Demonstration Project
Find out how YOU can become a participant.
www.NaturalSolutionsFoundation.org
Valley of the Moon™ Coffee
www.ValleyoftheMoonCoffee.org
Nano Silver: The Universal Antibiotic
www.Nutronix.com/naturalsolutions
StemEnhance: Increase Your Stem Cell Population Naturally
http://www.wealthbuilderssystem.com/site/index.asp?DL=140935&page=103264&ad=0
Detox Your Cells Naturally
http://www.detoxpads.com
http://salsa.democracyinaction.org/o/568/profile/login.jsp?redirect=%2Fo%2F568%2Fprofile%2Findex.jsp
Natural Solutions Foundation
The Voice of Global Health Freedom™
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Dr. Rima Reports: http://drrimatruthreports.com/?p=4850
DrRima.net
June 27, 2010
David Korten is both a change agent and an observer of change. He has written a provocative article called, :The Big Picture: 5 Ways to Know if You’re Making a Difference”.
He says that if you can answer “YES!” to ONE of the following criteria, you are making a difference.
Here are his criteria, taken from the article which you can read below:
1. Does it help discredit a false cultural story fabricated to legitimize relationships of domination and exploitation and to replace it with a true story describing unrealized possibilities for growing the real wealth of healthy communities?
2. Is it connecting others of the movement’s millions of leaders who didn’t previously know one another, helping them find common cause and build relationships of mutual trust that allow them to speak honestly from their hearts and to know that they can call on one another for support when needed?
3. Is it creating and expanding liberated social spaces in which people experience the freedom and support to experiment with living the creative, cooperative, self-organizing relationships of the new story they seek to bring into the larger culture?
4. Is it providing a public demonstration of the possibilities of a real-wealth economy?
5. Is it mobilizing support for a rule change that will shift the balance of power from the people and institutions of the Wall Street phantom-wealth economy to the people and institutions of living-wealth Main Street economies?
You, through the Natural Solutions Foundation, can answer
1. YES!!
2. YES!!
3. YES!!
4. YES!!
5. YES!! to this excellent assay of effectiveness.
Check out just a few of our accomplishments below and here, http://drrimatruthreports.com/?page_id=195. These accomplishments are yours and ours, together, because without you, there would be no meaning to our work. It is the community of empowered people that makes a difference, and that is what you, and we, are, together.
Frankly, our “Accomplishments” page is out of date because the Trustees of the Natural Solutions Foundation do not have time to get it up to date without taking time away from our rapid, profound and widely focused forward movement.
Consider: Our Codex eBook, http://drrimatruthreports.com/?page_id=220, was the first document to outline exactly how every country in the world, including, of course, the US!, could move to a higher standard for every class of food than Codex (which would not be hard!) without the dreaded World Trade Organization trade sanctions which are the club Codex waves to subdue countries that balk at degrading their food supply to make the globalists happy while their people die, just as we do, from toxic, degraded food and nutrients whose doses are so low that they have no beneficial impact worth noting – by design!
Our Codex DVD, “Nutricide“, http://drrimatruthreports.com/?page_id=156, is the lecture that has helped millions of people, including Codex delegates!, understand what Codex is about by understanding where it came from!
Our trips to the poorest countries all over the world resulted, for example, in their trusting our leadership so that we were able to block the US government’s attempt to get fluoride approved for inclusion at high levels in infant formula for normal babies at the Codex Committee for Nutrition and Foods for Special Dietary Uses (Thailand, 2007). This, alone, is a major victory in policy change!
The Natural Solutions Foundation, with its radio show, the Dr. Rima Reports, www.BlogTalkRadio.com/FreedomizerRadio, 9 PM to Midnight Eastern Standard Time, every Sunday night, is getting information out. Just look at the lineup of guests for the next couple of months! http://drrimatruthreports.com/?p=4850
Our Action Items generate hundreds of thousands to millions of your emails to decision makers!
Our Blogs are widely circulated and passed from reader to reader around the world!
Our Videos, like
Nutricide, http://video.google.com/videoplay?docid=-5266884912495233634#
Should the US Get Out of Codex? http://www.youtube.com/watch?v=AfCni-LuR_c
The Globalist Genocidal Agenda, http://www.youtube.com/watch?v=Y8f2P4GCJL8&feature=related
and dozens of others at www.Youtube.com/NaturalSolutions give people deeply researched, and deeply important information that they can use and share, changing local and leadership opinion. They, too, are passed from person to person around the world!
Radio appearances (on shows like Alex Jones, Jeff Rense and dozens of others), documentary film appearances (like “Making a Killing, Psychiatry, Industry of Death, and two of Governor Jesse Ventura’s Conspiracy Theories episodes, and other public information activities get the word out there. Uniquely, Natural Solutions Foundation gives people meaningful actions they can take – including growing their own food at www.FoodFreedomeJournal.org, for example.
And, uniquely among all the health freedom organizations we know of, we are actually creating a project to help the farmers of the world, the consumers of the world and the governments of the world to reclaim the production of clean, unadulterated food! It is called The Valley of the Moon™ Eco Demonstration Project, www.NaturalSolutionsFoundation.org, and it is a major forward step for people who want to live, to farm, to help or to enjoy a truly sustainable teaching community the temperate, beautiful Highlands of Panama.
Several governments have asked us to work with them to change their food supply to a clean, unadulterated, health-promoting one and, of course, we said “YES!”
On the eve of our departure for another grueling Codex meeting. Oh, Geneva is OK as a city. There are some decently priced restaurants for locals and the lake, surrounded by mountains is pretty enough. If I had my way, though, and if General Stubblebine had his, we would stay right here in Panama working on the development of the Valley of the Moon Eco Demonstration Project, www.NaturalSolutionsFoundation.org, getting ready for the Grand Opening of the Natural Solutions Center on August 7 and 8! By the way, consider this your invitation to join us for this event! If you are on the Health Freedom Action eAlert list (sign up here: www.HealthFreedomUSA.org) you’ll get all the details.
But we cannot stay here, much as we would like to. Hundreds of thousands of people -and more – want to know what the Codex Alimentarius Commission is doing to despoil the world’s foods to bring about the perpetual war on their bodies, their health and their freedom – indeed, their very existence, that Big Pharma, WHO, Big Chema and the other genocidal, callous and much-worse-than indifferent players on the global food scene, led by the US, of course. They wait for our live radio reports, our daily Codex Video and written updates and our analysis of what is happening so they can counter it.
They know, and they take action on, the dangers that bills like S. 510, the Food Fascism Bill (named, of course, the “Food SAFETY Bill”), http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=26714, will bring to them if they remain inactive. And we’ve kept this horrible bill from being voted on since November, 2009! That’s impact.
They are willing to call for a complete ban on the dangerous technology which has invaded the world’s food and non-food plant and animal life forms – including US, our DNA. By clicking on this link, rapidly growing numbers of people are protecting their future, and that of every living thing on the planet: http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=2049
Millions of people demanded that they have the right NOT to receive the vaccine for the absurd and fraudulent “Level 6 Pandemic” nonsense known as H1N1 or Swine Flu and the US backed off from requiring mandatory vaccination.
Now we are demanding Congressional hearings and responsibility in controlling, stopping and reversing the loss of children because of devastating environmental toxicity, including vaccines that do not work, have no science behind them and are killing us and our kids, while rendering huge numbers of us infertile, http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=3688. And we are suing the FDA to prevent more vaccines from being used which have never, ever been either tested to make sure that they are safe OR effective, let alone both. That case, the Stop The Shot Case, is a companion case to the Ear Candle Case, which we are also suing the FDA in that one, too. http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=2521. You see, if they can innocuous ear candles, of which 20 million have been sold without a single meaningful adverse event, saying that they are a medical device for which there is no medical use, they can ban ANY device or nutrient claiming the same.
We backed them off this crazed behavior in March, 2008 when they first flew this particular idea to see what would happen. What happened was that we, 688,000 strong, roared NO!, HELL NO! They predictably went away and, just as predictably, came back with this absurd power-grab to make all natural health products and services illegal.
We were there that time, and we are there this time, too. By the way, your recurring tax deductible donations here, http://drrimatruthreports.com/?page_id=189, are the essential lubricant which allows the health freedom wheels to keep turning. These donations are the only way that we can do this work, get to Codex, sue agencies, etc.
We are there, every time, because YOU are there. YOU are the netroots and YOU are the solution, the natural solutions. Thanks for making the Natural Solutions Foundation the largest health freedom organization in the world. And thanks for making a big, big difference.
Thanks, too, for your generous tax deductible donations. http://drrimatruthreports.com/?page_id=189
If you are not already giving the cost of a month’s worth of coffee, tea, chai, latte, cappuccino, or your other pleasure items each month, let me suggest that you do so, on a recurring basis. That’s the life-blood that keeps our brains and our other working parts pumping!!!!!
Oh, yes, two other things: first, if you use coffee for health or pleasure, you will want to taste the Valley of the Moon(TM) Coffee – FREE coffee! Coffee that we grow here in Panama to teach other farmers how to grow coffee without ANY toxic chemicals, neither herbicides like Monsanto’s Roundup(C), nor paraquat, nor Agent Orange products like 2-4D, nor pesticides or herbicides – NOTHING but sun, rain, fish meal and a 10 ingredient fermented compost! Other farmers are beginning to grow coffee this way, but there is nothing like our Valley of the Moon Coffee! Support your health and health freedom at the same time by making a tax deductible contribution and getting the healthy coffee. Oh, by the way, you can give this superb coffee as a thoughtful gift at any time of the year. Supplies are strictly limited so order NOW!
The second thing: All of this is great but without YOU as the person who disseminates this information, the Action Items and takes them once for each member of your family and then passes them along to all your contact, this information would stay the private knowledge of the few, a sort of information elite. Nice, but not effective. It is YOUR dissemination which makes this heath freedom thrust take wing and shape local, national and international policy.
It’s your world. Thanks for making us effective so that we do, in fact, make a difference!
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
www.DrRima.net
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Valley of the Moon™ Eco Demonstration Project
www.NaturalSolutionsFoundation.org
www.InternationalDecadeofNutrition.org
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The Big Picture: 5 Ways to Know if You’re Making a Difference
David Korten
David Korten’s newly revised and greatly expanded 2nd edition of Agenda for a New Economy: From Phantom Wealth to Real Wealth, outlines an agenda to create a new kind of economy: locally-based, community oriented, and devoted to creating a better life for all.
In this special pre-publication excerpt Korten explains how to tell if your actions are helping to build the new economy that “must be lived into being from the bottom up.”
For the many millions of us working to create a better world, it is easy to feel discouraged by the seeming insignificance of even major successes relative to the scale of the problems we face as a nation and a species. Consumed by the details and challenges of our daily engagements, we may easily lose sight of the big picture of the powerful social dynamic to which our work is contributing.
Step back from time to time; take a breath, look out beyond the immediate horizon to bring that big picture back into perspective. Reflect in awe and wonder at the power of the larger social dynamic to which your work contributes.
In my career in international development, I saw, time and again, that the most successful projects were not the largest or the most carefully, centrally planned; they were the ones that arose from the bottom up. Likewise, successful social movements are emergent, evolving, radically self-organizing, and involve the dedicated efforts of many people, each finding the role that best uses his or her gifts and passions. Their scope and their success may not, at first, be readily apparent. Social movements grow and evolve around framing ideas and mutually supportive relationships instead of through top-down direction. New ideas gain traction, or not, depending on what works for those involved in the movement. Some alliances are fleeting; others endure.
The organism, not the machine, provides the appropriate metaphor. The relevant knowledge resides not in the heads of outside experts but in the people who populate the system. The challenge is to help them recognize, organize, and use that knowledge in ever more effective ways.
This is the model I think of when I think about what it will take to build the New Economy—one based on fulfilling the basic needs of people and planet—that we need. It’s also the way that that economy is already being built: step by step, in creative and surprising ways, by people looking for alternatives to a system that isn’t working for them.
To bring down the institutions of Empire, we must begin to build the rules, relationships, and institutions of a New Economy. These must be lived into being from the bottom up.
So how do you know whether your work is contributing to a big-picture outcome? If you can answer yes to any one of the following five questions, then be assured that it is.
1. Does it help discredit a false cultural story fabricated to legitimize relationships of domination and exploitation and to replace it with a true story describing unrealized possibilities for growing the real wealth of healthy communities?
2. Is it connecting others of the movement’s millions of leaders who didn’t previously know one another, helping them find common cause and build relationships of mutual trust that allow them to speak honestly from their hearts and to know that they can call on one another for support when needed?
3. Is it creating and expanding liberated social spaces in which people experience the freedom and support to experiment with living the creative, cooperative, self-organizing relationships of the new story they seek to bring into the larger culture?
4. Is it providing a public demonstration of the possibilities of a real-wealth economy?
5. Is it mobilizing support for a rule change that will shift the balance of power from the people and institutions of the Wall Street phantom-wealth economy to the people and institutions of living-wealth Main Street economies?
These are useful guidelines for setting both individual and group priorities. Bear in mind that in a systems-change undertaking of this magnitude, there is no magic bullet and no one is going to make it happen on their own, so don’t be discouraged if the world looks much the same today despite your special and heroic effort yesterday. It took five thousand years to create the mess we are in today. It will take more than a few days to set it right.
David Korten adapted this article from the newly revised and expanded 2nd edition ofAgenda for a New Economy: From Phantom Wealth to Real Wealth, available for advance purchase from the YES! Magazine web store.
David is co-founder and board chair of YES! Magazine, co-chair of the New Economy Working Group, president of the People-Centered Development Forum, and a founding board member of the Business Alliance for Local Living Economies (BALLE). His books include Agenda for a New Economy: From Phantom Wealth to Real Wealth, The Great Turning: From Empire to Earth Community, and the international best seller When Corporations Rule the World.