Please pass this article along to anyone who thinks that vaccinations, especially mandated vaccinations, are good sense, good health and good public policy.
To learn more, click here (http://drrimatruthreports.com/index.php?page_id=699) to order your highly informative Vaccine Exemption eBook.
Vaccines are profitable only when used in large populations. But are they safe? And are they justified either by disease reduction or by in-use cost? The sober answers may surprise you if you are an advocate of vaccines.
Please share this careful analysis of the current vaccination mandates and practices in use nationally (and here examined through the lens of New Jersey vaccine policy, including opposition to conscientious exemption by parents) with everyone who is a vaccine adherent or supporter. Whether you share this important document with your child’s pediatrician, other parents, your local civil rights lawyer or others currently supportive of the unfounded myths that vaccines are safe and effective, please urge them to read this document carefully. Unlike the unthinking parroting or slick “junk science” praise of the supposed merits of vaccines and vaccinations, this article takes the allegations of safety and social use for vaccines on point by point and examines each of them using science and logic, not emotion, to look at each of the points raised by the Department of Health and Senior Services in New Jersey to justify their staunch opposition to allowing exemptions to vaccination on the basis of conscience.
The result is a very important article Dr Dr. King, a consultant who examines pharmaceutical options and evaluates them. Please reproduce it and send it electronically or in hard copy to everyone concerned, either pro, con or undecided, with the vaccination debate, including State legislators and Federal ones as well. And remember, these issues are NOT just about children. They are about vaccines and freedom concerning each and every one of us. Remember that on July 23 and 24, 2008, respectively, the Department of Health and Human Services and the Department of Homeland Security announced that their intention was to vaccinate every man, woman and child in America against Avian Flu, “…starting with those who want it.”
Vaccines and freedom can only co-exist if their use is totally voluntary. Anyone determining what you -or your children MUST – allow to be introduced into your body is abridging your freedom so deeply that you literally have none since if your autonomy does not include what happens to your body, your autonomy no longer exists.
The article is a detailed review of the response of the NJ Department of Health and Senior Services (DHSS) to the possibility of a law offering conscientious exemption opportunities to parents and others who do not wish to participate in vaccine programs.
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‘The Position of the New Jersey Department of Health and Senior Services (NJ DHSS) on: The Pending New Jersey Conscientious Exemption Legislation’ (NOTE: ALL RESPONSES OF THE DHSS ARE IN BOLD FACE IN THE FOLLOWING REVIEW OF THEIR POSITION ON THIS LEGISLATION – REL)
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Should anyone reading this draft find any significant factual error for which you have published substantiating documents, please submit that information to this reviewer so that he can improve his understanding of factual reality and appropriately revise his views and the final review.
A Draft Response To: “The Position of the New Jersey Department of Health and Senior Services (NJ DHHS) on: The Pending New Jersey Conscientious Exemption Legislation”, as transcribed by the reviewer, Paul G. King, PhD, on 5 November 2008 ….
This response to the NJ DHSS’ position on NJ S1071 addresses the “genuine concern” side for the safety and effectiveness of NJ’s mandated vaccination program as well as the observed impacts of the conscientious and/or philosophical exemptions on the observed background rates for some vaccine-covered diseases in the 18 states with such exemptions as compared to the USA as a whole.
Thus, this response presents factual information that exposes the weaknesses in, and/or the apparent problems with, the broad generalizations made in the NJ DHSS’ position statement.
Lest any take this reviewer’s remarks as those of someone who is anti-vaccine, this reviewer again reiterates that, given the scientific information available to him, he currently supports national vaccination programs for those vaccines that have truly been proven to be both generally safe and at least societaly cost-effective, provided the individual parent’s constitutional right to “due process of law” is not abridged or ignored.
Having made his position as an advocate for:
a. Banning the use of mercury compounds in medicine to safen vaccines,
b. Vaccine safety, and
c. Societaly cost-effective vaccines
clear, this reviewer will now assess the statements made in: “The Position of the New Jersey Department of Health and Senior Services (NJ DHHS) on: The Pending New Jersey Conscientious Exemption Legislation”.
S1071 – Conscientious Exemption to Mandatory Immunizations
The New Jersey Department of Health and Senior Services is opposed to S1071, which provides for a conscientious exemption to mandatory immunizations.
Obviously, the NJ DHHS has made it clear that it “is opposed to S1071” and A260, legislation to provide New Jersey citizens with a limited conscientious exemption to New Jersey’s mandated vaccination programs.
Public health care and medical communities consider vaccinations one of the most important measures in improving the public’s health over the past 100 years.
While there is no dispute that “(p)ublic health care and medical communities consider vaccinations one of the most important measures in improving the public’s health over the past 100 years”, the facts are that, in the industrialized world, vaccines have been a <10% factor in the reduction of the common contagious diseases (where sanitation, hygiene, clean water, safe food, adequate housing account for 90-plus % of the decrease in childhood diseases before vaccines were mandated). Moreover, in less developed countries (e.g., India), repeated vaccination campaigns for diseases such as polio have failed to provide the reductions in polio cases and/or the "elimination" of polio seen in the USA and other industrialized nations). Currently, the evidence in today's USA is: our current vaccination programs have succeeded in reducing several acute childhood diseases and, increasingly, some other diseases - at the cost of creating epidemics of chronic disorders, syndromes and diseases that have a strong autoimmune/immune-system-disruption component (e.g., asthma, type 2 diabetes, childhood MS, neurodevelopmental disorders, and food allergies). Yet most of those "(p)ublic health care and medical communities" continue to: · Deny the preceding realities, · Actively suppress the scientific research establishing these realities, · Attack the character and credibility of those independent scientists who dare to publish the truth about these health realities, and · Publish articles: a) which are based on "junk" science, b) which use knowingly "perverted" study de- signs, or c) which rely upon easily manipulated epidemiological reviews where independent access to the data sets used is blocked or the data sets are "lost" - preventing independent researchers from verifying the soundness of the: · Data sets evaluated, · Study designs used, · Results reported, and/or · Conclusions drawn from those findings. New Jersey has historically only permitted religious and medical exemptions to school entry vaccine requirements.
Here, the NJ DHSS states what has been the New Jersey history without addressing the reality that an exemption for a “sincerely held religious belief” is: a) in essence, a “conscientious” exemption for those who adhere to any religion and b), therefore, an exemption that discriminates against those who are religiously agnostic or atheists – a probable violation of the equal protection guarantees for all Americans.
Were the State of New Jersey to enact this statute, which provides a general conscientious (philosophical) exemption, this statute would end this seemingly illegal form of discrimination.
Broad exemptions to mandatory vaccination weaken the entire compliance and enforcement structure mandating vaccines for school entry and continued attendance.
First, taking this statement at face value, the NJ DHSS is advocating for a position that borders on a
health dictatorship where the “health police” and not the constitutions of the United States of America (USA) and the State of New Jersey control the lives of New Jersey citizens.
Thus, the NJ DHSS appears to be advocating for a society in which the rights to bodily integrity and
informed consent are either non-existent or trampled under by the health care establishment for a “greater good” that essentially benefits the healthcare establishment and ignores the physical, financial, mental and spiritual health of the public that it claims to protect.
Given the wording used, “weaken the entire compliance and enforcement structure”, the NJ DHSS is apparently more concerned about strengthening their control over our children than it is about the overall and individual health of our children.
Second, in other “democratic” nations (e.g., Canada, UK, and Japan), high rates of vaccination compliance have been attained and, provided less-safe vaccines have not been knowingly supplied (e.g., the less expensive MMR vaccine the UK used even though it contained the dangerous Urabe strain of the mumps), these rates have been maintained without any need for general mandatory vaccination programs for their citizens.
Moreover, the flexible Japanese approach to vaccines and vaccination programs has been so successful that the first-year infant mortality rate (IMR) in Japan (2.80 deaths per 1,000 “live births” [all values are CIA 2008 estimates]) is less than half the IMR in the USA (6.30 deaths per 1,000 live births [IMR-UK = 4.93; IMR-Canada = 6.08]), and significantly, chronic childhood disorders and diseases (e.g., childhood asthma, childhood type 2 diabetes, childhood obesity) are not at the epidemic levels seen in the USA.
In fact, on average, the Japanese life expectancy is 4 years longer than the average life expectancy in the USA and, unlike the USA, the life expectancy in Japan is not beginning to decline.
Finally, in the 18 states with a general conscientious/philosophical exemption to vaccination, there is no substantiation of the claim that having “(b)road exemptions to mandatory vaccination” has greatly reduced vaccine uptake rates or led to higher average background disease rates for those vaccines that are apparently safe and at least societally cost-effective in actuality.
If vaccination requirements can be waived by a parent, one may argue that this dissolution sets precedent for other mandatory health screenings (e.g., hearing, lead, tuberculosis) or services to become optional.
In a democratic society that recognizes bodily integrity as a fundamental right, there should be no mandatory health screenings or services unless these is a compelling actual “communicable disease outbreak” reason for such and, even in such instances (e.g., a TB outbreak in a school), the parents should be given the choice of a non-invasive alternative (e.g., a chest x-ray for the TB example) or a definitive blood test (and, in this example, the cheap but problematic and, for some, medically dangerous TINE test should be banned).
Currently, the religious exemption already provides a means by which “vaccination requirements can be waived by a parent”.
Finally, since when is a person’s exercise of any granted legal option a “dissolution” of anything?
No highly or densely populated states in the Eastern United States permit a philosophical exemption to school vaccination requirements.
First, the states with an children-of-all-ages conscientious (philosophical) exemption are (in alphabetical order): 1) Arizona, 2) Arkansas, 3) California, 4) Colorado, 5) Idaho, 6) Louisiana, 7) Maine, 8) Michigan, 9) Minnesota, 10) New Mexico, 11) North Dakota, 12) Ohio, 13) Oklahoma, 14) Texas, 15) Utah, 16) Vermont, 17) Washington State, and 18) Wisconsin.
In addition, Missouri and Nebraska have a conscientious/philosophical exemption for child care entry only.
Though only 5 states [Maine, Michigan, Ohio, Vermont and Wisconsin] of the 18 provide a full “philosophical exemption” in the Eastern United States, one could argue that one of them, Ohio [11.5 million], which has a population one-third larger than New Jersey [8.7 million], is a “highly or densely populated state”.
However, California, the most populous state [36.5 million], and Texas, the second most populous state [23.9 million], both have philosophical exemptions with no evidence of a significant excess of disease cases in children for those vaccines that are vaccines against the disease (e.g., measles, mumps, rubella, polio, hepatitis B) or for vaccines against bacterial toxoids and/or toxins (the diphtheria and tetanus toxoid components and the toxic substances in the acellular pertussis preparations) in the diphtheria, pertussis and tetanus combination vaccines (see Table “1” in the published article or the abbreviated version that follows).
[Note: The cases data was taken from the Florida Department of Health’s April 2008 “Task Force Requests to the Florida Department of Health” report to the Florida Governor’s Task Force on
Autism Spectrum Disorders. The population numbers used are based on the published population data at: http://en.wikipedia.org/wiki/List_of_U.S._states_by_population.]
Abbreviated Table “1”: 2006 Comparison of Vaccine-Preventable Disease Cases, Among States with Philosophical Exemptions for Immunizations, Florida andU.S.
State Measles* Mumps** Rubella*
or USA (incidence/ 100,000) (incidence/ 100,000) (incidence/ 100,000)
——— ———————– ———————- ———————-
Arizona 0 40 (0.63) 0
Arkansas 0 8 (0.28) 0
California 6 (0.016) 31 (0.085) 1 (0.003)
[12% of US]
%of US Total 10.9 0.471 9.09
[% of 12%] [90.9] [3.93] [75.8]
Colorado 1 (0.021) 51 (1.04) 0
Idaho 0 7 (0.47) 0
Louisiana 0 3 (0.07) 0
Maine 0 0 0
Michigan 1 (0.001) 84 (0.079) 1 (0.001)
Minnesota 1 (0.019) 180 (3.46) 0
New Mexico 0 3 (0.152) 0
North Dakota 0 14 (2.19) 0
Ohio 0 45 (0.392) 0
Oklahoma 0 10 (0.276) 0
Texas 0 58 (0.243) 0
[7.8% of US]
% of US total 0.88%
[% of 7.8%] [11.4%]
Utah 0 5 (0.189) 0
Vermont 0 0 0
Washington 2 (0.031) 42 (0.649) 0
State
Wisconsin 0 842 (15.0) 0
Total of 18
states 11 (0.008) 1,423 (1.09) 2 (0.0015)
% of US Total 20.0 21.6 18.2
[% of 36%] [55.6] [60.0] [50.5]
{% of 42.5% {47.1} {50.8} {42.8}
est. pop % of the 18 states}
Florida 4 (0.022) 15 (0.082) 1 (0.005)
[6% of US]
% of US Total 7.3 0.23 9.1
[% of 6%] [122] [3.8] [152]
U.S. Total 55 (0.180) 6,584 (2.15) 11 (0.004)
* Confirmed Cases **Confirmed and Probable Cases
In contrast, Florida, the fourth most populous state and one that has no philosophical exemption, shows some evidence that not having a philosophical exemption has led to more than expected cases of measles and rubella cases but a less than expected mumps and pertussis cases (two diseases not well-controlled by the vaccines [the MMR and DTaP/Tdap vaccines] containing components for these two diseases).
Thus, for those diseases well-controlled by their vaccines and for which low levels of cases are still
being reported, it would seem that the states with “philosophical exemptions” have, on average, a lower disease incidence rate than: a) the overall average for the USA and b) the rate for Florida, the fourth most populous state.
Thus, the two most populous states as well as 16 other states have a conscientious/philosophical exemption and less than expected disease levels for those diseases that are well-controlled by vaccines.
Therefore, based on the preceding realities, every state should have a conscientious/philosophical
exemption.
Moreover, like New Jersey, the citizens of New York, the third most populous state [19.3 million], are
also seeking legislation providing this exemption to its citizens.
Based on all of the preceding realities, the evidence favors having a “philosophical exemption” in New Jersey, the eleventh most populous state [8.7 million].
New Jersey has numerous characteristics that make it particularly vulnerable to vaccine-preventable disease, which include a high population density, past history of multiple vaccine-preventable disease outbreaks affecting children, a highly mobile population, high numbers of recently arrived immigrants, and its “corridor state” nature.
As long as there is good sanitation, hygiene (including personal hygiene and hot-water washing for soiled undergarments and bedding), clean air, clean water, and adequate nutrition and housing, none of the cited factors make New Jersey “particularly vulnerable to vaccine-preventable disease”.
When it comes to high population density, the much higher population density in Japan, a nation with less than half the infant mortality as the USA, clearly shows that this factor is not significant unless the aforementioned basics are compromised.
Since there is no post-vaccine-adoption history of any vaccine-preventable epidemic in New Jersey for any disease for which the current mandated vaccine is truly long-term protective, localized sporadic disease outbreaks are:
· A red herring or
· A clear indication that the available vaccines are
not in-use effective in some instances.
Since:
· There are other states, including California and Texas (the two most populous states) that have a
“philosophical exemption” and “a highly mobile population” and a “high numbers of recently arrived immigrants” (including much larger numbers of illegal immigrants),
· Three of these 18 states, Arizona, California, and Texas, are also conscientious/ philosophical exemption states that are also corridor states for the majority of illegal immigrants entering the USA,
and
· None of these states have overall disease rate averages (for those diseases that are truly vaccine-preventable diseases) that are significantly higher than the overall rates for the USA, all of these factors are “red herrings” in today’s USA.
Particularly in light of New Jersey’s special traits, the highest number of children possible must receive vaccines to protect them and others.
Given the data for the states that have conscientious/philosophical exemption and special factors similar to those raised in this NJ DHSS statement, the data do not:
· Support the NJ DHSS’ assertion that “the highest number of children possible must receive vaccines”,
or
· Provide evidence that the mandated vaccines “protect” the implicit children who receive these vaccines or the unidentified “others”.
Vaccines not only protect the child being vaccinated but also the general community and the most vulnerable individuals within the community, including those too young to be vaccinated, the elderly, the immunocompromised, and those who have medical contraindications to vaccination – this fact is well-documented in scientific literature.
The NJ DHSS’ unsupported assertion that “Vaccines not only protect the child being vaccinated but also the general community and the most vulnerable individuals within the community”, is at odds with the reality that inoculation of children with the currently recommended live-virus vaccine components (measles, mumps, rubella, herpes varicella zoster, 3 bioengineered strains of human influenza, and 5 strains of human-cow hybridized rotavirus or a human rotavirus) puts all of the uninoculated and unprotected individuals with whom these recent inoculees have contact at risk of contacting these viral diseases that those inoculated shed after they are inoculated.
For example, although the CDC asserts that all children become “immune” to the human rota virus by the time they are five years of age, the studies on the human-hybrid rota virus reported that up to one-third of “supposedly rota virus-immune” adults who come into contact with a child recently inoculated with this rota virus vaccine (Merck’s RotaTeq®) may contract a case of rota virus – a possibility that some parents have reported experiencing as an all-too-real reality.
Moreover, the use of vaccines that clearly do not protect the children inoculated (the influenza vaccines that offer no real protection to children under 2 years of age and marginal protection to children under 5 years of age) based on a claim that this practice will protect the elderly is not only not supported by the published science on the epidemiology of human influenza but also, if it were true, would amount to an abnormal society where, to “protect” the health of the elderly:
· Children are knowingly put at risk (see the influenza-vaccine-related adverse events, including death, seen for all influenza vaccine formulations, that are reported in the Vaccine Adverse Events Reporting System (VAERS) database) and
· The healthcare establishment supports the knowing mercury poisoning of children, which clearly occurs when Thimerosal-preserved influenza vaccines are given to children, pregnant women and nursing mothers and probably occurs when any Thimerosal-containing influenza vaccine is given to pregnant women and/or children because, though the safe dose for Thimerosal in any vaccine has never been established:
· Mercury poisoning has been established in young children who have been given toxic doses of
Thimerosal-preserved serums and/or vaccines, indirectly (in the womb) and directly (in early
childhood), and have subsequently been diagnosed with a neurodevelopmental disorder in the autism spectrum [1] where the mercury bolus doses from the serums and vaccines represent not less than
50% of the mercury dose received by an effected child from conception to age 3, and
· Persistent Thimerosal-derived mercury toxicity has been seen in monkeys [2] (and other mercury-sensitive animals [3]) given just the doses of Thimerosal or one of its ethyl mercury metabolites that, in some instances, mimicked the Thimerosal doses that children given Thimerosal-preserved vaccines at 2, 4 and 6 months would receive under the vaccination schedules recommended in the USA from 1999 through 2001.
Finally, for influenza, the epidemiological evidence is that human influenza viruses are neither highly contagious [4] nor, as discussed in the same reference, easily transmitted from those infected to those who are well – even in close communal groups, including families.
[1] a. Geier DA, Kern JK, Garver CR, Adams JB, Audhya T, Nataf R, Geier MR. Biomarkers of environmental toxicity and susceptibility in autism. J Neurol Sci. 2008 Sep 24. [Epub ahead of print]
b. Geier DA, Mumper E, Gladfelter B, Coleman L, Geier MR. Neurodevelopmental disorders, maternal
Rh-negativity, and Rho(D) immune globulins: a multi-center assessment. Neuro Endocrinol Lett.
2008 Apr; 29(2): 272-280.
c. Nataf R, et al. Poryphyrinuria in childhood autistic disorder: implications for environmental
toxicity. Toxicol Appl Pharmacol. 2006; 214: 99-108.
d. Geier DA, Geier MR. A prospective assessment of porphyrins in autistic disorders: a potential marker for heavy metal exposure Neurotox Res. 2006; 10: 57-64.
e. Young HA, Geier DA, Geier MR. Thimerosal exposure in infants and neurodevelopmental disorders: an assessment of computerized medical records in the Vaccine Safety Datalink. J Neurol Sci. 2008 Aug 15; 271(1-2): 110-118. Epub 2008 May 15.
[2] Burbacher TM, et al. Comparison of blood and brain mercury levels in infant monkeys exposed to methyl-mercury or vaccines containing Thimerosal. Environ. Health Persp. 2005; 113(8): 1015-1021.
[3] a. Laurente J, Remuzgo F, Ãvalos B, Chiquinta J, Ponce B, Avendaño R, Maya L. [Neurotoxic effects of thimerosal at vaccines doses on the encephalon and development in 7 days-old hamsters.] An Fac Med Lima 2007; 68(3): 222-237.
b. Shiraki H, Nagashima K. Essential Neuropathology of Alkylmercury Intoxication In Humans from the Acute to the Chronic Stage with Special Reference to Experimental Whole Body Autoradiographic Study Using Labeled Mercury Compounds. Neurotoxicology 1977; 1: 241-260.
c. Tryphonas L, Nielsen NO. Pathology of chronic alkylmercurial poisoning in swine,” Am J Veter.
Res. 1973; 34(3): 379-392.
d. Takahashi T, Kimura T, Sato Y, Shiraki H, Ukita T. Time-Dependent Distribution of 203Hg-Mercury Compounds in Rat and Monkey as studied by Whole Body Autoradiography. Eisei Kagaku [Japanese: J Hygienic Chem.] 1971; 17(2): 93-107.
[4] Cannell JJ, Zasloff M, Garland CF, Scragg R, Giovannucci E. On the epidemiology of influenza.
Virol J. 2008 Feb 25; 5: 29. [Among the issues this paper addresses, this recent electronically published review article reports the lack of high sick-to-well infectivity for human influenza.]
As an example, in a Journal of the American Medical Association study published in 2000, investigators found that children who did not receive measles and pertussis vaccines for philosophical or religious reasons were 22 times more likely to contract measles and 6 times more likely to get pertussis; also, schools with higher numbers of exempted children were associated with more outbreaks that had community wide-implications.
First, the referenced, but not cited, article’s text appears to be more self-serving propaganda than it is important information because the locations, time periods, and diseases chosen seem to have been knowingly chosen to result in the preordained outcomes that the study was “designed” to find.
Second, the locations in which the researchers at the Centers for Disease Control and Prevention (CDC) chose to do this study (in some counties in Colorado) were areas with relatively small populations as compared to the population of the USA (some percentage of Colorado’s population that overall is only about 1% of the population of the USA) that were/are not representative of the population of the USA or the U.S. population’s overall risks of contracting “vaccine-preventable” diseases.
Though the NJ DHSS fails to cite the study reference, based on a search of “PubMeD”
(http://www.ncbi.nlm.nih.gov/sites/entrez), the abstract of the study apparently referenced states (with CAPITALIZATION added for emphasis):
“1: JAMA. 2000 Dec 27;284(24):3145-50. Links Comment in:
JAMA. 2000 Dec 27;284(24):3171-3.
JAMA. 2001 Mar 28;285(12):1573-4.
JAMA. 2001 Mar 28;285(12):1573; author reply 1574.
Individual and community risks of measles and pertussis associated with personal exemptions to immunization. Feikin DR, Lezotte DC, Hamman RF, Salmon DA, Chen RT, Hoffman RE. Respiratory Diseases Branch, Centers for Disease Control and Prevention, 1600 Clifton Rd, MS-C23,
Atlanta, GA 30333, USA. drf0@cdc.gov
CONTEXT: The risk of vaccine-preventable diseases among children who have philosophical and religious exemptions from immunization has been understudied. OBJECTIVES: To evaluate whether personal exemption from immunization is associated with risk of measles and pertussis at individual and community levels. DESIGN, SETTING, AND PARTICIPANTS: Population-based, RETROSPECTIVE COHORT STUDY USING DATA COLLECTED on standardized forms REGARDING ALL REPORTED MEASLES AND PERTUSSIS CASES AMONG CHILDREN AGED 3 TO 18 YEARS IN COLORADO DURING 1987-1998.
MAIN OUTCOME MEASURES: Relative risk of measles and pertussis among exemptors and vaccinated children; association between incidence rates among vaccinated children and frequency of exemptors in Colorado counties; association between school outbreaks and frequency of exemptors in schools; and risk associated with exposure to an exemptor in measles outbreaks. RESULTS: Exemptors were 22.2 times (95% confidence interval [CI], 15.9-31.1) more likely to acquire measles and 5.9 times (95% CI, 4.2-8.2) more likely to acquire pertussis than vaccinated children. AFTER ADJUSTING FOR CONFOUNDERS, THE FREQUENCY OF EXEMPTORS IN A COUNTY WAS ASSOCIATED WITH THE INCIDENCE RATE OF MEASLES (RELATIVE RISK [RR], 1.6; 95% CI, 1.0-2.4) AND PERTUSSIS (RR, 1.9; 95% CI, 1.7-2.1) IN VACCINATED CHILDREN. Schools with pertussis outbreaks had more exemptors (mean, 4.3% of students) than schools without outbreaks (1.5% of students; P =.001). AT LEAST 11% OF VACCINATED CHILDREN IN MEASLES OUTBREAKS ACQUIRED INFECTION THROUGH CONTACT WITH AN EXEMPTOR. CONCLUSIONS: The risk of measles and pertussis is elevated in personal exemptors. Public health personnel should recognize the potential effect of exemptors in outbreaks in their communities, and parents should be made aware of the risks involved in not vaccinating their children.”
Apparently, since none were reported, there were no severe adverse outcomes in any group of children based on the reported 2006 data.
In addition, though this study did report these relative risks for disease as: “Exemptors were 22.2 times (95% confidence interval [CI], 15.9-31.1) more likely to acquire measles and 5.9 times (95% CI, 4.2-8.2) more likely to acquire pertussis than vaccinated children.” it also reported: “After adjusting for confounders, the frequency of exemptors in a county was associated with the incidence rate of measles (relative risk [RR], 1.6; 95% CI, 1.0-2.4) and pertussis (RR, 1.9; 95% CI, 1.7-2.1) in vaccinated children”, indicating that, after the confounding factors were removed, neither of these relative risks was statistically significant (requiring a RR of 2.0 or larger) and, because no other diseases were mentioned, there was no “exemption” effect for the other diseases covered by the MMR vaccine (mumps and rubella) or the DTaP vaccine (diphtheria and tetanus).
Though not mentioned by the NJ DHSS here, the most important fact in this article was: “At least 11% of vaccinated children in measles outbreaks acquired infection through contact with an exemptor” – indicating that, unlike having the measles once, the MMR vaccine is not effective in protecting all those given the MMR vaccine from subsequently contracting measles when exposed to the measles virus.
In the final analysis, there was/is really no statistically significant risk associated with exemptors (religious and medical) and, apparently, the CDC had/has no interest in conducting such studies in the more populous, densely populated, highly mobile, “corridor” states like New Jersey.
All vaccines currently licensed in the United States are safe and effective.
First, the NJ DHSS neither provides nor cites any studies that establish the validity of the preceding
statement.
Second, as cited in previous reviews [5], there is a large and growing body of evidence that some of the current FDA-licensed vaccines are neither truly population safe nor, in some cases, in-use effective even when the effectiveness criterion is loosened to only require that the vaccine be societally cost-effective including:
[5] These reviews are freely available for download from the “Documents” web page of the CoMeD Internet website: http://www.mercury-freedrugs.org/. For example, the most recent 2-part review, “A Draft Review of: ‘Florida Governor’ Task Force on Autism Spectrum Disorders- Task Force Requests to the Florida DoH’, Part 1 (17 October 2008; 68 pages)” and “A Draft Review of: ‘Florida Governor’ Task Force on Autism Spectrum Disorders- Task Force Requests to the Florida DoH’, Part 2 (17 October 2008; 77 pages)” [along with the report that was reviewed, “Florida’s Governor’s Task Force on Autism Spectrum Disorders – Task Force Requests to the Florida DoH (16 Sept. 2008; 49 pages)”], contains a detailed analysis of the current childhood vaccination programs that dispassionately assesses the in-use medical cost-effectiveness of the current vaccines and their associated vaccination programs.
The Current Recommended National Human Influenza Vaccination Program
Published studies have clearly established that the influenza vaccination program is not in-use effective in children, adults and the elderly for a variety of reasons.
Moreover, the majority (greater than 75 %) of the available doses contain a level of Thimerosal that has not been proven safe to administer to either children or adults.
Therefore:
· New Jersey’s mandate for vaccination of young children should be rescinded,
· The current recommended national program for influenza should be abandoned,
· The human influenza vaccines should be removed from the list of vaccines covered by the National Vaccine Injury Compensation Program (NVICP), and
· All petitions filed with the NVICP from the time the influenza vaccines were added to the list of compensable vaccines until 3 years after the vaccine was recognized to be not effective and removed from the national vaccination program should be automatically paid, with the government assessing the manufacturer of the putative causal human influenza vaccine for the costs of that compensation because the human influenza vaccines are not effective drugs.
The Current Recommended National Herpes Varicella Zoster Vaccination Program
Since:
· The recommendations for a national varicella vaccination program were based on an unfulfilled promise of marginal societal cost-effectiveness PROVIDED: a) one dose would produce lifetime protection, b) the vaccine was assumed to cause no serious side effects, and c) the vaccination program would not increase shingles cases,
· The CDC is now recommending 2 doses because one dose has failed to control “wild” chickenpox cases,
· Shingles cases in both children and adults have increased and
· The vaccine has not only the highest level of VAERS- reported adverse side effects of any single-component vaccine but has also been shown to cause serious conditions in some who are vaccinated, it is obvious that the chickenpox vaccination program is not societally cost effective.
Thus,
· The recommendation for inclusion of “varicella” (chickenpox) in the national vaccination program should be rescinded,
· New Jersey should remove it from its list of mandated vaccines for children,
· Varicella should be removed from the list of NVICP-covered vaccines, and
· All petitions filed with the NVICP from the time the varicella vaccine was added to the list of compensable vaccines until 3 years after the vaccine was recognized to be not societally cost-effective and removed from the national vaccination program should be automatically paid, with the government assessing the manufacturer of the varicella vaccines for the costs of that
compensation because, though all drugs, including vaccines, are required to be by U.S. law to be both safe and effective, the varicella vaccines are not effective.
The Current Recommended National Rotavirus Vaccination Program
Because:
· The current rota virus vaccination programs have not significantly reduced the risk of severe adverse
effects (intussusception, Kawasaki’s, and pneumonia) in the inoculees as compared to the unvaccinated,
· The vaccines are live virus vaccines that not only infect those inoculated but also, at a high rate,
those who come into contact with recent inoculees or their fecal waste and
· The costs of the vaccine and its administration greatly exceed the societal cost-effectiveness
level established in the 1990s even after correcting for inflation, it is obvious that the rota virus vaccination programs are not societally cost-effective in the USA.
Thus,
· The recommendation for inclusion of rotavirus in the national vaccination program should be rescinded and rota virus removed from the list of NVICP-covered vaccines,
· New Jersey should not add rotavirus to its list of mandated vaccines, and
· All petitions filed with the NVICP from the time the rota virus vaccine was added to the list of
compensable vaccines until 3 years after the vaccine was recognized to be not societally cost-effective and removed from the national vaccination program should be automatically paid, with
the government assessing the manufacturer of the offending rota virus for the costs of that compensation because, though required by law to be both safe and effective, the rota virus vaccines are clearly not in-use effective.
At best, all that the rota virus vaccines do is give clinical cases of the rota virus strains in the vaccines to those inoculated with no significant reduction in either the number or severity of cases of
rota virus compared to the unvaccinated population, even in the carefully contrived clinical trials where the lack of reduction in life-threatening outcomes in the vaccine arm over the unvaccinated arm was perversely turned into positive because, although some of those inoculated had these life-threatening side effects, the elevation in their level was not statistically significant.
Thus, the licensing and approval of the human-bovine rota virus vaccine rests on a knowing perversion of the reality that, to be effective, the vaccine should have produced a statistically significant reduction in the level of cases for these life-threatening adverse effects.
However, like the previous vaccine, Wyeth’s RotaShield®, the current live-virus rotavirus vaccines, Merck’s RotaTeq® and GlaxoSmithKline’s Rotarix® did not significantly reduce the incidence of the following life-threatening adverse outcomes:
· Intussusception (for either of these vaccines).
· Kawasiki’s [6] (for the RotaTeq vaccine), or
· Pneumonia (for the Rotarix vaccine,
even though the test populations for the Phase 3 clinical trials were selected to be in areas where the back-ground rate of disease was significant to mask the level of harm caused by vaccination so that it would not produce a statistically significant increase in life-threatening outcomes.
[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.
The Current Recommended National Vaccination Programs For Other Vaccines
For discussions of other vaccines, the reader should study the prior applicable posts on the
CoMeD website: http://www.mercury-freedrugs.org/.
The Department only mandates vaccines licensed by the FDA and recommended for universal use by the Centers for Disease Control and Prevention’s (CDC) Advisory Committee on Immunization Practices, American Academy of Pediatrics, and other government and professional organizations.
While the preceding states what the NJ DHSS is doing vis-Ã -vis setting vaccination mandates, one should note that these actions are seemingly at odds with the NJ DHSS’ constitutional duty to only support the use of preventive medicines, including vaccines, that are proven to be effective in protecting the health of New Jersey citizens – a duty that the NJ DHSS and elected state officials, including the governor, have obviously failed to discharge in those instances where vaccines, which have been proven to be in-use ineffective, are being mandated for New Jersey’s children.
The Department, medical experts and practitioners believe that using available vaccines is highly preferable to control individual cases and outbreaks of vaccine-preventable diseases.
Here, it is unambiguous that the “Department, medical experts and practitioners believe” in what they are doing.
Unfortunately, public health policy should not be based on what the NJ DHSS, “medical experts and
practitioners believe”.
Public health policy should only be based on proof that the mandated vaccines are safe and in-use cost-effective when all the costs (including the costs of the adverse events associated with the vaccination program for them) are accurately assessed and included.
Thus, the NJ DHSS should:
· Abandon its unsupported belief-based policies, which have elevated vaccination to quasi-religious prominence, and
· Return to mandating only those vaccines that, based on in-use outcomes that include the costs
of the adverse reactions to a given vaccine or vaccine component and the need for “boosters” and their risks, are proven safe and at least in-use societally cost-effective for New Jersey’s children.
For many of these diseases, effective therapies are not available to treat sick individuals or are ineffective when given at the time of diagnosis.
Since the mandated childhood vaccines are supposedly intended to “protect against” “native” diseases by giving the children:
· “Weakened” strains of the disease (e.g., the live-virus measles, mumps, rubella, varicella,
rotavirus and influenza vaccines),
· Inactivated strains of the disease (e.g., the inactivated-virus polio and influenza vaccines),
· Manufactured components derived from superficial components of the disease organisms (e.g., the hepatitis B, hepatitis A, meningococcal, pneumo-coccal, and HPV vaccines), or
· The modified toxins (“toxoids”) or toxic components produced by the disease (e.g., the diphtheria, tetanus, and pertussis vaccines), the NJ DHSS’ broad “(f)or many diseases” generalization here is, at best, problematic.
Moreover, for those diseases for which the available preventive vaccines have not been shown to be
truly in-use cost-effective, it is wrong to waste public health dollars vaccinating our children because, at best, the vaccine only postpones the age at which our children contract the disease – a move that, for some of the contagious viral childhood diseases, only increases the probable severity of the disease as well as the costs to treat that disease in those instances where our children finally contract that disease.
In addition, the NJ DHSS’ statement ignores:
· The potential long-harm to our children’s developing immune system that injecting them with
vaccines containing not only the disease-related components but also other immune-system-reactive components may cause in some of those injected,and
· The long-term immune-system imbalance that occurs when our developing children are abnormally exposed to disease components by injection rather than by the “natural” exposure routes.
Furthermore, though it is clear that aluminum-based adjuvants may over-stimulate the macrophagic portion of the immune system and, for some, lead to autoimmune disorders and increased susceptibility to some chronic medical conditions, vaccine formulations containing such aluminum-based adjuvants (or other adjuvants that are known to be capable of causing immune-system dysfunction) continue to be approved when, by increasing the level of the disease-related antigens or making other formulation changes, it is, or should be, possible to make an effective vaccine without adding any adjuvant.
Finally, even though the vaccine makers have, as the U.S. Food and Drug Administration (FDA) and the vaccine makers have repeatedly admitted [7], failed to prove that the Thimerosal in Thimerosal-preserved vaccines is safe to the explicit “sufficiently nontoxic …” standard required by law in 21 C.F.R. §610.15(a) and such Thimerosal-preserved drugs are “deemed adulterated” drugs under 21 U.S.C. §351(a)(2)(B), the FDA and the vaccine makers have colluded to continue to approve and market these adulterated vaccines to the American public.
[7] Subcommittee on Human Rights and Wellness, Committee on Government Reform of the House of Representatives, “Mercury in Medicine Report – Taking Unnecessary Risks,” Washington, DC, as published in the Congressional Record, pgs. E1011- E1030, May 21, 2003.
Thus, the NJ DHSS’ decision to be an active party to the preceding collusive actions that expose our children to adulterated vaccines is particularly egregious in the case of the inactivated influenza
vaccines given to our children, where:
· Several publications, including: Geier DA, King PG, Geier MR. Influenza Vaccine: Review of
Effectiveness of the U.S. Immunization Program, and Policy Considerations, Journal of American
Physicians and Surgeons, 2006 Fall; 11: 69-74, have established that the influenza vaccines are
not in-use effective,
· Several studies have clearly established that Thimerosal is not an effective preservative in
any vaccine formulations that contains proteins or other sulfur-containing compounds,
· More than a dozen recent studies have established that injection of Thimerosal-preserved vaccines mercury poisons all of those injected to varying degrees,
· Most of the available doses of these inactivated influenza vaccines are still unnecessarily pre-
served with Thimerosal or contain a lower level of Thimerosal that has been proven to be toxic to
our children, and, worse,
· Studies have shown that daily supplementation with vitamin D-3 [8] apparently protects almost all
adults who take daily 2000-IU vitamin D-3 supplements during the influenza season against most all
strains of influenza while, at best, the current influenza vaccines only provide limited protection:
· For a few of the probable circulating influenza virus strains,
· To only some of those inoculated with them.
[8] Preventive dietary supplementation with vitamin D-3 (1,000 to 5,000 IU per day depending on the child’s or adult’s size, skin color, age, sun exposure, and overall health) has been proven to protect against contracting all strains of human influenza (while the vaccines, at best, only protect against a few strains of influenza) as well as to have other health benefits. [Note: The short-duration administration of high-doses of vitamin D-3 (ca. 50,000 IU per day) has also been shown to be effective in treating influenza cases. References: a. Cannell JJ, Hollis BW. Use of vitamin D in clinical practice. Altern Med Rev. 2008 Mar; 13(1): 6-20. b. Cannell JJ, Vieth R, Umhau JC, Holick MF, Grant WB, Madronich S, Garland CF, Giovannucci E. Epidemic influenza and vitamin D. Epidemiol Infect. 2006 Dec; 134(6): 1129-1140.]
Thus:
q IF the NJ DHSS were truly interested in preventing cases of influenza, as this statement asserts,
q THEN the NJ DHSS would be mandating that all children and the elderly be: a) appropriately tested for their level of vitamin D-3 and b), based on the test results, given an appropriate added daily dose of vitamin D-3 during the “flu” season, which the NJ DHSS would then supply for each child whose family could not afford the cost.
Though diseases still occur among the vaccinated, many more vaccine-preventable illnesses would occur if fewer persons were vaccinated.
Here, the NJ DHSS’ statement is a classic example of Orwellian doublespeak – a statement that begins with a muted truth, “diseases still occur among the vaccinated” – which embodies the reality that even multiple doses of the current vaccines do not provide either short-term or long-protection to all those who have been vaccinated against contracting these diseases when those fully (multiply) vaccinated with them are exposed to the actual disease – and connects that truth to an unclear statement, “many more vaccine-preventable illnesses would occur if fewer persons were vaccinated”, that falsely speaks of “more vaccine-preventable illnesses”.
However, for “vaccine-preventable illnesses”, the truth is:
· There could only be more cases of the illnesses that are claimed to be “vaccine-preventable” – not more “illnesses” (diseases) and
· The evidence is clear that the current USA recommended vaccination programs are, for whatever reasons, major causal factors for the current epidemics of chronic childhood medical conditions (e.g., asthma, severe food allergies and intolerances, type 2 diabetes, MS, certain leukemias, idiopathic dilated cardiomyopathy (IDCM), obesity, and neurodevelopmental and behavioral disorders) that were either rare or non-existent in our children before 1980.
The return and resurgence of vaccine-preventable diseases translates to significant economic and human costs related to time lost from work, medical care, and public health interventions.
Since, except for smallpox, the diseases of which the NJ DHSS speaks have not been reduced to laboratory specimens in every nation on the Earth, it is false to speak of the “return and resurgence of vaccine-preventable diseases” when all that is happening in the USA today, for those diseases where the vaccines seemingly provide effective “long-term” protection, are sporadic isolated outbreaks.
Moreover, except for the disease cases caused by herpes varicella zoster, most of these outbreaks in the USA are being triggered by exposure to recentlyinfected carriers coming from countries where, for whatever reason,
· The native disease is still endemic, or
· A recent live-virus-vaccine inoculee was sheddingthe vaccine’s live viral components and infected
the carrier just before their return to the USA, and
· Those exposed to these returning outbreak initiators:
· Were not vaccinated or,
· If vaccinated, were not adequately protected from contracting the disease by the vaccinations they received.
Second, the actual data for those diseases that the federal government and the NJ DHSS have labeled
“vaccine-preventable diseases” fails to show any nationwide disease resurgence for those few diseases for which the vaccines apparently are at least in-use societally cost-effective.
Third, the “economic and human costs” from the chronnic illnesses that the USA’s current vaccination programs have engendered are orders of magnitude greater than the short-term “economic and human costs” for the current levels of these acute childhood diseases (e.g., measles, mumps, rubella, diphtheria, tetanus, pertussis [whooping cough], rota virus and pneumonia).
The more exemptions we allow, the more difficult it will be to prevent vaccine-preventable diseases from affecting our communities.
The data presented by the Florida Department of Health along with the added information provided to address incidence levels and relative disease levels to address the “philosophical exemptions” issue (see Abbreviated Table “1”) does not support the NJ DHSS’ assertion that the “more exemptions we allow, the more difficult it will be to prevent vaccine-preventable diseases …” in today’s America in the 18 states, including the two most populous states, California and Texas, that have a “conscientious/philosophical exemption” option.
Hopefully, after reviewing this response and the referenced and cited publications, the NJ DHSS will not only drop its opposition to S1071 (and A260) and support the passage of this legislation, but also immediately revoke its mandates for influenza vaccination and, after reviewing the in-use effectiveness data for each of the currently mandated vaccine components, adjust the vaccination mandates to eliminate those other vaccines that are not in-use cost effective, starting with the current vaccines for herpes varicella zoster and rota virus.
Finally, after reviewing this response and all of the cited publications, if the NJ DHSS ignores any of the factual realities set forth in this review, then the people of the state of New Jersey should, in mass, rise up and demand that the New Jersey State Legislature pass and the Governor of the State of New Jersey sign into law a statute that:
q Repeals all vaccination mandates, and
q Simply states that:
All vaccination programs shall be voluntary, and
For those vaccines that are truly provably cost-effective:
· The state will provide the vaccine doses for all of it residents, vaccination programs where vaccination is provably societally cost-effective by truly independent investigators, and
· The NJ DHSS will initiate and support programs for all of the alternative disease-preventive measures, including:
· Better hygiene and sanitation,
· Dietary supplementation and healthy diets, which have been proven to reduce the risk of the initiation and spread of communicable-disease outbreaks,
· Setting the state’s recommendation for daily intake of vitamin D-3 to no less than 1,000 IU (25 micrograms), and
· Requiring:
o All school-related health-screening blood tests include an assessment of serum 25-hydroxy-vitamin D levels, and
o The healthcare provider to furnish or prescribe appropriate vitamin D-3 supplement levels when the measured level is below 45 ng per milliliter (mL) of serum with appropriate follow- ups to ensure that the child’s serum 25-hydroxy-vitamin D levels exceed 45 ng per mL.
Concluding Remarks
As a supporter of vaccines and vaccination programs that are reasonably safe and at least societally cost-effective, the author understands that the current New Jersey mandated vaccination programs have severe problems, which the NJ DHHS should immediately address.
Moreover, the NJ DHSS should address the problems with its vaccination program mandates in a manner that is:
· Truly public-health cost-effective and
· Free of the pernicious influence of those who directly and/or indirectly profit from:
· More vaccines and/or
· Expanding mandated vaccination programs that are intentionally blind to the rise in, and the costs of, the chronic childhood diseases, which the affected children and their families must bear for the rest of their lives.
If the NJ DHSS fails to act in the responsible manner being recommended, then the NJ DHSS should be prepared to be the proverbial “last straw” that will trigger a movement to repudiate all vaccination mandates because it will be knowingly ignoring the actual fiscal and physical harm that its scientifically indefensible vaccination mandates have caused, are causing and will cause.
Finally, in conjunction with this response, the NJ DHSS should carefully study the in-depth two-part review of the September 2008 report issued by the Florida Department of Health, and the report itself, as posted in the “Documents” section on the CoMeD Internet website: http://www.mercury-freedrugs.org (see footnote 5).
About the Reviewer:
Information about this reviewer, Paul G. King, PhD, can be found on the Internet at:
http://www.dr-king.com/.
This reviewer received no compensation for this review; and, other than his advocacies, has no
conflicts of interest.
*It is not medical advice and it does not require any specific action or actions.*
*While the information is thought to be accurate, no representation is made as to the accuracy of the information posted other than it is my best understanding of the facts on the date that this email and any attachments thereto are posted. Everyone should verify the accuracy of the information provided for themselves before acting on it.
**************************************************************************************************
Dr. King http://www.dr-king.com
**************************************************************************************************
FAIR USE NOTICE: The following review may contain quotations from copyrighted(©) material the use of which has not been specifically authorized by the copyright owner. Such material is made available for educational purposes, to advance reader’s understanding of human rights, democracy, scientific, moral, ethical, social justice and other issues. It is believed that the author’s quoted statements are a ‘fair use’ of this copy- righted material as provided for in Title 17 U.S.C. section 107 of the US intellectual property law. This material is being distributed without profit.
There are two articles which follow this introduction which have great bearing on your health and, eventually, your ability survive.
Agricultural chemicals have been known since their inception to pose significant threats to human, animal and environmental health. They are, in fact, only approved for use on the food supply of people and animals because, in my opinion, of the enormous wealth which chemical companies, which are, in essence, a branch of the pharmaceutical industry, have have available to throw at compliant regulators and legislators, plus deceptive and misleading advertising bulwarked by corporate junk science.
Agricultural chemicals are not, however, limited to herbicides, fungicides, pesticides and fertilizers. Other chemicals quality for that designation, too. For many years, the US has permitted the spraying of fluoride and mercury on crops after harvest to prevent mold growth during storage despite the well characterized dangers of those substances.
Now, another toxin, also well known for its adverse effect on the brain, the nervous system, the endocrine system, perception, mood and vascular integrety has been approved by the supposed guardians of our health, the FDA, EPA and USDA for direct application, without any upper limit, on our foods.
Read this article and ask yourself whether you ever want to eat non organic food again. Then ask yourself why regulators are permitting known toxins in our food.
And then click on this link (http://drrimatruthreports.com/index.php?page_id=189) to make a donation to the Natural Solutions Foundation, a totally donation-supported Non governmental organization (NGO) devoted to your right to make your own choices in your health. Among the freedoms that we believe belong to you and that we are fighting for on your behalf, and ours, is the right to know what your food has been sprayed with, genetically modified with, contaminated with or irradiated with. In short, if food is contaminated you have a right to know it.
And you have another right, too, as I see it.
You have a right to be protected by the regulators from the self-interested companies that do not care at all about the damage their chemicals and processes bring to you and yours. That is, after all, what we believe regulatory agencies are supposed to do. But the sad truth is that we need to be protected FROM the regulatory agencies.
That’s one of the things that Natural Solutions Foundation does, in fact. And, of course, we need your help. Click here (http://drrimatruthreports.com/index.php?page_id=189) to become a supporting sponsor with a tax deductible recurring donation. And visit the Natural Solutions Foundation home page, www.HealthFreedomUSA.org, to sign up for our free, secure Health Freedom eAlerts.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
MSG is being sprayed right on fruits, nuts, seeds, grains, and vegetables as they grow —
even those used in baby food
In the 1970s, reluctant food processors “voluntarily” took processed free glutamic acid (MSG) out of baby food. Today it’s back, in fertilizers called “Omega Protein Refined/Hydrolyzed Fish Emulsion” and “Steam Hydrolyzed Feather Meal,” both of which contain hydrolyzed proteins; and in a product called AuxiGro WP Plant Metabolic Primer (AuxiGro) produced by Emerald BioAgriculture (formerly Auxein Corporation), which contains both hydrolyzed protein(s) and “monosodium glutamate.” AuxiGro is being sprayed on some of the vegetables we and our children will eat, into the air we and our children must breath, and onto the ground from which it can move into drinking water. Head lettuce, leaf lettuce, tomatoes, potatoes, and peanuts were among the first crops targeted. On September 12, 2000, the Auxein Corporation Web site gave the following information:
Crops registered include: Celery; Fresh Market Cucumbers; Edible Navy and Pinto Beans; Grapes; Bulb Onions; Bell, Green and Jalapeno Peppers; Iceberg Head Lettuce; Romaine and Butter Leaf Lettuce; Peanuts; Potatoes; Snap Beans; Strawberries; Processing Tomatoes; Fresh Tomatoes; and Watermelons.
Today, there is no crop that we know of that has not been approved for treatment with MSG by the U.S. Environmental Protection Agency (EPA).
Even in California — the only state where there are any restrictions on the use of AuxiGro — AuxiGro has been approved for use on a number of crops, and Emerald BioAgriculture continues to push for more. Field tests in California have been — and may continue to be — conducted on a variety of crops, and those AuxiGro treated crops may be sold in the open market without revealing that they have been treated. We can’t tell you which crops those are because the CDPR has refused to send records of test trials (which are public information) to the Truth in Labeling Campaign.
As of June 13, 2002, AuxiGro was registered for use in California on tomatoes, almonds, apricots, cherries, plums, nectarines, peaches, prunes, grapes (including grapes to be used in wine), and onions. At that time, the California Department of Pesticide Regulation said they were not aware of any testing of AuxiGro for use on other crops. They also said that they did not have any proposals presently in house to register additional crops for AuxiGro. It would appear, however, that what the CDPR said was not true, for the CDPR subsequently announced that Emerald BioAgriculture had applied for permission to use AuxiGro on tomatoes (new use), and on melons (new crop) — and, to the best of our knowledge, approval is always preceded by field testing.
On July 7, 2004, Emerald BioAgriculture requested approval of use of AuxiGro as a desiccant, disinfectant, fertilizer, fungicide, growth regulator – for increased yield and prevention of powdery mildew in various crops such as almonds, grapes, and melons. They also asked to add cole crops (including broccoli, brussels sprouts, cabbage, cauliflower, kale, collards, turnips, rutabaga, mustard, watercress, and kohlrabi) to the list of crops approved for AuxiGro use.
Approval for use on organic crops–in all states–has been requested.
What’s wrong with using glutamic acid, an amino acid found in protein, as a spray on crops?
– In protein, amino acids are found in balanced combinations. Use of free glutamic acid as a spray on crops throws the amino acid balance out of kilter.
– It’s not the glutamic acid found in protein that is being sprayed on crops, it’s a synthetic product. The spray being used most widely is called AuxiGro. The “free glutamic acid” or so called “L-glutamic acid” component being used by its manufacturer, Emerald BioAgriculture, contains L-glutamic acid, an amino acid found in protein; but it also contains D-glutamic acid, pyroglutamic acid, and other chemicals referred to in the industry as “contaminants.” The free glutamic acid used in AuxiGro is processed free glutamic acid. It is manufactured — in chemical plants — where certain selected genetically engineered bacteria — feeding on a liquid nutrient medium — excrete the free glutamic acid they synthesize outside of their cell membrane into the liquid medium in which they are grown. In contrast, the free glutamic acid found in protein, and the free glutamic acid involved in normal human body function, are unprocessed. free glutamic acid, and contain no contaminants.
– No one knows what the long term effects of spraying processed free glutamic acid on crops will be.
– That the processed free glutamic acid (MSG) will be absorbed into the body of the plant and into the fruit, nuts, seeds, or vegetable it produces seems undeniable. If it were not, the plant would not be stimulated to grow. Neither Emerald BioAgriculture or the EPA will address this issue.
– That there will be residue left on crops has not been disputed by Emerald BioAgriculture. But no study of either the amount of that residue, or the least amount of processed free glutamic acid needed to cause a reaction in an MSG-sensitive person, has ever been done. “It should wash off” doesn’t mean it will wash off. “It seems unlikely that such a small amount would cause a reactions” doesn’t mean that a small amount will not cause a reaction or have long term health effects.
– Free glutamic acid is known to be toxic to the nervous system. But the neurotoxic effects that processed free glutamic acid will have on animals that consume the plants on which it is sprayed – effects over and above any effects caused by external glutamic acid residue – have never been evaluated. Neither are there data on the effects that spraying processed free glutamic acid will have on drinking water.
– Consider, also, that children are most at risk from the effects of processed free glutamic acid. Their undeveloped blood-brain barriers leave them most at risk from exposure to processed free glutamic acid. It has been repeatedly demonstrated that infant animals fed processed free glutamic acid when young develop neuroendocrine problems such as gross obesity, stunted growth, and reproductive disorders later in life, and that they also develop learning disabilities. Emerald BioAgriculture did not address that particular safety issue in its application to the EPA.
– No one knows how little glutamic acid is needed to kill a single brain cell or to trigger an adverse reaction.
– Free glutamic acid is a neurotransmitter. It causes nerves to fire, carrying nerve impulses throughout the nervous system.
– Free glutamic acid is a neurotoxin. Under certain circumstances, free glutamic acid will cause nerves to fire repeatedly, until they die.
– Processed free glutamic acid kills brain cells. The free glutamic acid ingested by laboratory animals that caused brain lesions and neuroendocrine disorders was very often given in the form of the food ingredient “monosodium glutamate.” “Monosodium glutamate” is the name of a particular food additive. Processed free glutamic acid is the reactive component in “monosodium glutamate,” just as processed free glutamic acid is a reactive component in AuxiGro.
The glutamate industry research done in the 1970s that was submitted to the EPA by the Auxein Corporation, that pretended to find that processed free glutamic acid is “safe,” has been long refuted by independent scientists. Indeed, at the present time, neuroscientists attempting to develop drugs to block the toxic effects of free glutamic acid are using processed free glutamic acid to selectively kill certain kinds of brain cells.
– Processed free glutamic acid causes neuroendocrine disorders in maturing animals that ingest processed free glutamic acid early in life.
– Processed free glutamic acid causes learning disorders in maturing animals that ingest processed free glutamic acid early in life.
– Processed free glutamic acid crosses the placental barrier and causes learning disabilities in animal offspring of dams that ingest it.
– Processed free glutamic acid has access to the brain through the blood-brain barrier, which is not impervious to the unregulated flow of processed free glutamic acid. The blood-brain barrier is immature at birth and may continue to develop up to puberty. In certain areas called the circumventricular organs, the blood barrier is never impervious to the unregulated flow of free glutamic acid. In addition, the blood-brain barrier is easily damaged by such events as high fever, a blow to the head, drug use, stroke, ingestion of processed free glutamic acid, and the normal process of aging.
– The National Institutes of Health recognize glutamic acid as being associated with addiction, stroke, epilepsy, degenerative disorders such as Alzheimer’s disease, Parkinson’s disease, and ALS, brain trauma, neuropathic pain, schizophrenia, anxiety, and depression.
– For years, free glutamic acid has been produced and used in food additives with names such as monosodium glutamate, sodium caseinate, and hydrolyzed soy protein. In some people, the processed free glutamic acid in food additives causes adverse reactions that include migraine headache, asthma, arrhythmia, tachycardia, nausea and vomiting, depression, and disorientation. The processed free glutamic acid in prescription and non-prescription drugs, food supplements, and cosmetics can also cause adverse reactions.
There are badly flawed industry-sponsored studies that have pretended to find that processed free glutamic acid does not cause adverse reactions. Inappropriate procedures used by the glutamate industry have included limiting subjects to people virtually guaranteed not to be sensitive to processed free glutamic acid, and/or using processed free glutamic acid or other similarly reactive substances in placebos as well as in test material. The Food and Drug Administration (FDA) has based its claim that processed free glutamic acid causes only mild and transitory reactions on those badly flawed industry-sponsored studies.
– Even the EPA admits that the food additive called “monosodium glutamate” causes adverse reactions.
– Even the FDA admits that the food additive “monosodium glutamate” contains processed free glutamic acid.
<>– Even the FDA admits that many consumers refer to all free glutamic acid as “MSG.”
The EPA’s approvals of use of MSG in agriculture are simple, straightforward, and in violation of the Federal Food, Drug, and Cosmetic Act
In reviewing the application of Auxein Corporation (now Emerald BioAgriculture) for use of processed free glutamic acid in a spray to be applied to crops as they grow, the EPA failed to conform to the requirements of the Federal Food, Drug and Cosmetic Act, which require, in part, that the EPA review any proposed action for validity, completeness, reliability, and relationship to human risk. The EPA also ignored Executive Order 13045 which requires government agencies to consider available information concerning the variability of the sensitivities of major identifiable subgroups of consumers, including infants and children. For example, Auxein Corporation sent the EPA 14 industry-sponsored toxicological studies from the literature, all done in the 1970’s, but failed to mention hundreds of studies in the literature that refuted those 14 studies. Auxein Corporation even failed to send the EPA independent studies that appeared in the same book(s) as the industry-sponsored studies sent to the EPA. For example, although processed free glutamic acid causes brain lesions and neuroendocrine disorders in infant animals, this special hazard faced by infants was ignored by Auxein Corporation. It would appear that Auxein Corporation restricted its consideration of “available information” to information made available by the glutamate industry; and the EPA, even after having been sent abstracts from other “available information,” has not challenged the Auxein Corporation applications. A more complete discussion of the shortcomings of the EPA approvals granted to Auxein Corporation has been submitted to the EPA.
Questions about the safety of spraying processed free glutamic acid on plants and into the environment have been raised by the Truth in Labeling Campaign and by individual consumers. The EPA has refused to address those concerns. The EPA, and, in particular, EPA spokesperson Dr. Janet Andersen, has failed to respond to allegations that in approving the spraying of processed free glutamic acid, the EPA failed to consider the reliability, validity, and completeness of the Auxein Corporation application or comply with Executive Order 13045 entitled Protection of Children from Environmental Health Risks and Safety Risks, except to say that the EPA had complied with executive order 13045. Moreover, while responding to letters that asked direct questions of the EPA, Andersen failed to respond to most, if not all, of the direct questions contained in those letters.
AuxiGro, the first MSG-laced plant “growth enhancer” to hit the market, has been approved for spraying on every crop we know of, with no restrictions on the amount of processed free glutamic acid (MSG) that may remain in and/or on crops when brought to market. Even before consumers had an inkling that crops were being sprayed, the Truth in Labeling Campaign received reports that MSG-sensitive consumers had gotten sick from head lettuce and potatoes.
Federal Register notices chronicling the application and approval of processed free glutamic acid are available on the Web via GPO Access, the Federal Register, through: http://www.gpoaccess.gov/fr/index.html. Application for approval of use of AuxiGro was made to the EPA in 1997. Testing of the product was also approved in that year, and many of the test crops sprayed with AuxiGro were brought to market without notifying consumers. Glutamic acid was granted an exemption from establishment of a tolerance limit in January, 1998. AuxiGro was also approved for use on a number of crops in January, 1998, and approved for use on other crops later. No announcement of these approvals was made in the Federal Register.
Due to a technical glitch in the system, the glutes came to need one more approval to make their California registrations work. The glutes were asking for AuxiGro to be approved for use as a fungicide in California, but the EPA had only approved AuxiGro for use as a pesticide produce or plant growth enhancer. And when application was made for this addition to their approvals, the application was brought to our attention; and the Truth in Labeling Campaign filed a formal protest to this approval of AuxiGro. The Formal Objection of the Truth in Labeling Campaign was filed on August 16, 2001 with the EPA.
By law, formal objections filed in a timely manner must be responded to within six months. Also, by law (we were told) even though the Final Rule had not been promulgated, this additional use of AuxiGro would be considered approved unless and until the EPA determined that it should be otherwise. In July, 2004, we received a conference call from Dr. Andersen and a number of other EPA players, including an EPA lawyer — a “courtesy call” telling us that our objections had been discounted and that the Final Rule allowing use of AuxiGro as a fungicide would be published shortly in the Federal Register.
What’s wrong at the EPA?
Neither the EPA nor Janet Andersen, Ph.D., director of the Biopesticides and Pollution Prevention Division (BPPD), are stupid. Rather, all evidence would appear to suggest that the EPA, which is charged with protecting the health of Americans, says it is protecting the health of Americans, when in fact the EPA acts to protect the bottom line of big business. Don’t think for a moment that MSG is the only toxin unleashed on the American public by the EPA. Let the words “methyl parathion” and “DDT” jog your memory.
The EPA, in granting the chemical referred to as “L-glutamic acid” an exemption from the requirement of a tolerance for residues of “L-glutamic acid” on all food commodities when applied/used in accordance with good agricultural practices (thereby allowing unrestricted amounts of processed free glutamic acid (MSG) residue to remain in and on any and all food crops that come under the EPA’s jurisdiction) violated Section 408(c)(2)(A)(i), Section 408(c)(2)(ii), Section 408(c)(2)(B), and Section 408(b)(2)(D) of the Federal Food, Drug, and Cosmetic Act.
Neither “L-Glutamic Acid and Gamma Aminobutyric Acid; Exemptions from the Requirement of a Tolerance; Final Rule” (Federal Register June 21, 2001) nor “Glutamic Acid; Pesticide Tolerance Exemption; Final Rule” (Federal Register January 7, 1998), which preceded it, met the criteria established by law for granting exemptions from the restriction of a tolerance.
How did spokesperson Andersen excuse the fact that the EPA approved processed free glutamic acid for use in an EPA approved spray? First, said Andersen, the free glutamic acid used in the spray is naturally occurring, and it’s 99.3 per cent pure pharmaceutical grade L-glutamic acid. Yet, in admitting that the free glutamic acid in AuxiGro is not 100 per cent pure L-glutamic acid, and that it is pharmaceutical grade, Andersen contradicted herself, and actually made the point that 1) if the free glutamic acid used in AuxiGro were truly natural, it wouldn’t be “pharmaceutical grade;” and 2) if the free glutamic acid used in AuxiGro were truly natural it would be 100 per cent, not 99.3 per cent pure L-glutamic acid.
Andersen said something else very interesting. She said that the EPA is well aware of the fact that MSG causes adverse reactions. However, when Andersen used the term “MSG” she was referring to the one food ingredient called “monosodium glutamate,” and not to the free glutamic acid in “monosodium glutamate” that causes adverse reactions. Failure to define terms, as Anderson did (and does) so handily, is both deceptive and misleading.
What Andersen did is very clever. What she said makes no sense at all. No one has ever claimed that the processed free glutamic acid in AuxiGro comes out of a box labeled “monosodium glutamate.” So for her to say it doesn’t, is meaningless. On the other hand, the claim has been made that the free glutamic acid in AuxiGro will cause the same brain lesions, neuroendocrine disorders, adverse reactions and other diverse disease conditions that are caused by the free glutamic acid in “monosodium glutamate” and the other food additives that contain processed free glutamic acid. That claim is true, but Andersen does not address it. How do you refute someone who ignores legitimate questions and spews out irrelevant statements as though they pertained to your legitimate questions? You don’t. The EPA defense of its approval of use of processed free glutamic acid in plant “growth enhancers” and its registration of AuxiGro has two parts to it: 1) ignoring those who question EPA actions, and 2) making the irrelevant statement that AuxiGro does not contain MSG (monosodium glutamate).
Neither Andersen nor anyone else at the EPA ever addressed the criticism that approvals given by the EPA to allow the use of free glutamic acid and the product AuxiGro were inappropriate.
The EPA, which approved the used of processed free glutamic acid in plant “growth enhancers,” made a grievous error. But instead of recognizing and remedying that error once it was pointed out to them, the EPA began a cover-up. That cover-up included use of ambiguous words and phrases, half-truths, and downright lies told to consumers. The cover-up continued (and continues still) with a variation of those ambiguous words and phrases, half-truths, and downright lies told to legislators who inquire about spraying MSG into the environment.
You might find the Emerald BioAgriculture sales literature interesting
Sales literature promoting AuxiGro was once found on their Web site, but is now long gone. While Federal Register notices included the fact that there is processed free glutamic acid (MSG) in AuxiGro, the sales literature from Auxein Corporation did not mention the fact that their product contains free glutamic acid until the Truth in Labeling Campaign began to broadcast that information. In November, 1999, Auxein added deceptive, misleading, and untrue statements in an elaboration of its Product Page, wherein they essentially make the untrue assertion that the glutamic acid used in AuxiGro is chemically and biologically identical to that found in plants and animals.
Sales literature did (on September 12, 2000), however, contain the following:
“PRECAUTIONARY STATEMENTS
HAZARDS TO HUMAN AND DOMESTIC ANIMALS – CAUTION”
If you think you might be reacting to AuxiGro sprayed on crops, you might want to try to (contact Emerald BioAgriculture (formerly Auxein Corporation) at the addresses that follow. (A friend recently told us that he tried to contact them by e-mail, but his e-mail was returned unopened.) By law, the company is required to forward reports of adverse reactions to the EPA. You might want to ask the EPA if Emerald BioAgriculture did so.
John L. Mclntyre, Ph.D.
President & CEO
Emerald BioAgriculture (formerly Auxein Corporation)
3125 Sovereign Drive, Ste. B
Lansing, MI 48911-4240
Phone: (888) 828-9346
Fax: (517) 882-7521
E-Mail: mailto:%20sales@auxein.com
(From time to time, their web page, http://www.auxein.com , can be accessed by password only.)
www.Truthout.org
Evidence of poison
Fiona Macleod
08 March 2007 11:59
A Limpopo medical doctor has documented a string of physical abnormalities — including
breasts on a five-year-old girl — that he believes are directly linked to the unregulated
use of agricultural chemicals.
Dr Johan Minnaar (44) has produced evidence of serious illnesses and disorders among his
patients in Groblersdal, where commercial farmers are spraying large amounts of
pesticides on crops.
Horrific cases include teenage boys temporarily “growing breasts” during spraying
seasons, miscarriages, partial facial paralysis, cancers and ear malfunctions. Many of his
patients suffer from milder poisoning symptoms, such as asthma, sinusitis, headaches,
dizziness and depression.
Minnaar, who has been practising as a doctor in Groblersdal since 1997, took the unusual
step of coming forward with his evidence after unsuccessful attempts to get government
and regulatory authorities to intervene.
He said: “Groblersdal is surrounded by farms growing mostly citrus and grapes, but also
cotton, vegetables and maize. Throughout the year there is constant crop spraying with
pesticides containing organophosphates and carbamates. No one has informed the
community what pesticides are being used, even though the law states people must be
notified before spraying.”
Minnaar started investigating after realising that symptoms he had experienced over six
years followed a pattern.
“I experienced chronic fatigue, nausea, muscle aches and pains, skin rashes and arthritis,
particularly from August till November, when there is a noticeable increase in the spraying.
On investigation, it became clear that other people had these symptoms at the same time.”
Last August, he became so ill that he had to stay at home for two weeks. His wife and
three children also showed symptoms. He began regularly testing his and his spouse’s
blood and the tests showed they were exposed to organophosphates and carbamate
pesticides.
Minnaar laid complaints with the registrar of the national agriculture department, the
water affairs department and the labour and health departments of the Limpopo
government. He also tackled the farmers, chemical companies and crop sprayers.
The spraying continued and, on two days in February this year, large amounts of
carbamate were released during the aerial spraying of citrus orchards. Residents were not
warned beforehand. Among those who later showed signs of poisoning were pupils of two
schools located in the orchards.
Minnaar said pupils regularly played on the sports fields during spraying. The teenage
boys who had consulted him about “growing breasts” in the spraying seasons attended the
schools.
In late January, a woman brought a five-year-old girl who had developed breasts to his
consulting rooms. Minnaar suspected it could be linked to poisoning and referred her case
to Limpopo government officials, who he met two days later.
“As with many patients, she had no access to medical facilities or funds. The authorities
undertook to get her medical testing and treatment, but we’ve heard nothing,” he said.
According to Professor Leslie London of the University of Cape Town’s health sciences
faculty, premature puberty and other hormonal abnormalities are symptoms of
contamination by pesticides containing “endocrine disruptors”.
A 2005 study of girls in Mexican farming areas, titled Altered Breast Development in Girls,
indicated that pesticides could affect breast development and lead to early puberty.
Said London: “It has been shown that endocrine disruptors can also affect sexual
maturation and differentiation. A study in Sri Lanka of a pesticide called endosulfan found
that boys living in villages below cashew nut plantations sprayed with endosulfan had
impaired sexual maturity and other reproductive impairments.”
London researched aerial crop spraying around Groblersdal in 2005, with a focus on risks
to small farmers rather than health impacts. Last year, he published research on possible
links between aerial organophosphate spraying in the Northern Cape and Guillain-Barré
Syndrome, a neurological disorder.
“The problem of rural towns affected by agricultural application of pesticides is
ubiquitous,” he said. “Present regulatory and safety management methods really don’t
address this problem sufficiently.
“I think there is a view that if you choose to live in the country, you should accept this as a
way of life. That is a societal value decision, not a matter of science.”
The health department’s directorate of environmental health has announced plans to
launch a chemical safety programme in Groblersdal at the end of March. According to its
draft concept document, “the aim is to launch the programme to inform provinces that
national [government] is willing to assist them in the management of chemicals”.
The draft programme identifies schoolchildren, women, farmers and farmworkers, shack
dwellers, informal traders and manufacturers as the “most vulnerable communities in
municipalities that lack capacity to properly and satisfactorily deal with chemical safety
issues”.
South Africa is a signatory to international conventions aimed at promoting chemical
safety, and the labour ministry said in October that chemical safety was “high on the
minister’s agenda”. But crop spraying is a highly technical industry, and pinpointing
contamination is difficult.
London said it was almost impossible for applicators in planes to control the drift of
chemical sprays. “Aerial application has been shown in some studies to drift more than
2km, even in the absence of strong winds.”
European countries strictly regulate the industry through buffer zones around residential
areas and warning systems, he added.
Gerrit van Vuuren, an aerial application consultant at Croplife South Africa, blamed mist-
spraying of crops on the ground. “It is absolutely wrong to conclude that because there is
a yellow aircraft spraying agrichemicals in an area, it must the reason for ill health effects,”
he said.
Van Vuuren said mist-blowers apply more than 1 000 litres of spray mixture a hectare,
compared to 30 to 40 litres in the case of aerial spraying. They also blow a significant
volume of the spray higher than 6m into the air.
“A couple of mist-blowers spraying thousands of litres of spray mixtures at night are less
visible than an aircraft spraying a couple of hundred litres in the morning.”
He said it was up to farmers to notify inhabitants and issue warnings. They were also
supposed to ensure no one entered their fields during spraying.
The environmental health unit at the Elias Motsoaledi municipality, under which
Groblersdal falls, said it was “busy investigating the usage of pesticides being sprayed
from aeroplanes, as nuisances do occur from these activities”.
But Minnaar is frustrated by government promises to investigate. “For all practical
purposes, the supposed controls are not working. While they keep promising to sort it out,
we are getting poisoned,” he said.
UPDATE: Rally a Huge Success!
See: http://vitaminlawyerhealthfreedom.blogspot.com/2008/10/no-forced-vaccination-rally.html
Tell your State Representatives that you want strong exemptions from mandatory vaccination (Action Item works for you no matter which State you live in):
http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=21833
————–
This is the latest announcement about this Thursday’s Pro Health Freedom Rally in Trenton. Please forward this information to anyone in the region who can get to this important show of solid support for health freedom.
One Thousand People Expected To Rally For Vaccination Choice
at the State House in Trenton, NJ on Thursday, October 16, 2008 at 12:00 p.m.
NJ Assemblywoman Charlotte Vandervalk, Board-certified Pediatrician Dr. Lawrence Palevsky and National Vaccine Information Center co-founder Barbara Loe Fisher, will join NJ parents and professionals at a rally in Trenton for vaccination choice. Nearly one thousand people are expected, requiring Trenton to close the streets to accommodate the crowds.
The speakers represent a cross-section of society including medical doctors, nurses, chiropractors, scientists, clergy, educators, soldiers, politicians, journalists, autism activists, homeschoolers and many parents. The NJ Coalition for Vaccination Choice (NJCVC) invites you to rally with them by the steps of the State House, outside Gov. Corzine’s office.
The group opposes the four new vaccine mandates including an annual flu shot for children ages 5 and under, required for daycare and pre-school. NJCVC supports the passage of bill A260/S1071, a conscientious exemption to mandatory immunization which will permit parents to select all, some or no vaccinations for their children. A form of this parental right already exists in 19 other US states. All legislators will be in Trenton for a Special Session. Fox News plans to cover the event. Fox aired a live segment on vaccination choice in NJ on October 9 (see http://tinyurl.com/3nmgqb and http://tinyurl.com/45ca5y).
Press urged to cover this high visual impact event: signs, banners, balloons, photos, children, music, personal stories, legislator appreciation ceremony. Rally Information: Rain or Shine, Thursday, October 16, 2008, Noon- 2 pm, 125 West State Street, Trenton, NJ, www.njvaccinationchoice.org for more rally details.
Contact Louise Habakus vaxRSVP@verizon.net 917-553-4634.
Max will be speaking at the Rally. Natural Solutions Foundation Trustee Ralph Fucetola, representing the largest health freedom organization in the world, The Natural Solutions Foundation, will be speaking at the rally.
Max’s Storyhttp://www.youtube.com/watch?v=YswnGsfZsQI
Here is our anticipated
–x–x–
Natural Solutions Foundation
www.HealthFreedomUSA.org
Media Release: End All Forced Vaccination
Trenton, October 16, 2008 – Natural Solutions Foundation participates in the Rally for Vaccination Choice at the Statehouse in Trenton, New Jersey today. Through its www.HealthFreedomUsa.org web site, the Foundation is the largest international ‘netroots’ Health Freedom alliance in the world.
Foundation trustee and life-long New Jersey resident Ralph Fucetola JD delivered a special message to the Rally from Foundation President Maj. Gen. Bert Stubblebine (USA, ret) and Medical Director Rima E. Laibow, MD. The message stated,
“Natural Solutions Foundation supports the efforts of people around the world who oppose forced vaccination for any purpose. As an educational, nongovernmental organization we seek to inform legislators and decision makers about the dangers of vaccine induced disease and the necessity of a Universal Right to Vaccine Exemptions, including strong religious, philosophical and medical exemptions for all vaccines. We congratulate New Jersians on their efforts to stop the uninsurable risks of mandated vaccines.â€
Counsel Fucetola continued, “The fact that the insurance industry, our society’s experts in risk, will not insure vaccines is a very telling fact. Without the special Federal Vaccine Injury Compensation Program (VICP) tax that every person who is mandated to buy vaccines is forced to pay, there could be no mandated vaccines at all. Public companies cannot invest in uninsurable risks, so Congress, ever supine to the interests of Big Pharma, mandated that the victims have to pay a tax to guarantee pharmaceutical industry vaccine profits. So far, over two billion tax dollars has been paid out to the families of children maimed and killed by vaccines. This must stop now!â€
The Natural Solutions Foundation, along with other health freedom advocates, declared, a year ago, that ending forced vaccinations must be a top priority of all freedom activists. The Tiburon Statement, named after the California town where it was written at an emergency meeting of nongovernmental organizations, can be found at: http://drrimatruthreports.com/index.php?p=460 – it states:
Convening for Health Freedom of Choice, Protecting our Children from Forced Vaccination
Health and Freedom leaders and advocates, meeting in an emergency strategic session at Tiburon, California and electronically, declare –
– We collectively call upon Congress and State Legislatures to take immediate steps to restore and guarantee freedom of choice in vaccination and health care and to protect our children and us against forced treatments.
– The moral imperative embodied in the World Medical Association Declaration of Helsinki forbids involuntary medical treatment or experimentation in the absence of fully informed, voluntary consent.
– We have a right to legal protection against mandatory inoculations of our children, such as those which occurred on November 17, 2007 in Prince George’s County Court House, enforced by police.
– Taxpayers have paid nearly $2 billion to compensate families for the death or disability of their children due to vaccination.
We, the undersigned, call upon the Congress of the United States and legislators of each State to adopt the strongest possible legal protections to ensure health care freedom of choice, including the universal right to vaccination exemptions.
Further information: Ralph Fucetola JD- ralph.fucetola@usa.net – http://vitaminlawyerhealthfreedom.blogspot.com/
Stop Mandatory Vaccination. Take all of the following Action Steps:
The Natural Solutions Foundation has been fighting mandatory vaccination, vaccination disinformation (e.g., vaccines are safe and effective) and all other compulsory health intrusions, like restrictions on free speech, unlabeled GMO Franken Foods, since its inception.
Here’s what we are doing about it:
1. We’ve created reliable information sources you can access and you can trust:
* Our highly informative Vaccination Exemption eBook (http://drrimatruthreports.com/index.php?page_id=699) gives you information you simply will not find anywhere else
* The vigorous Yahoo! No-Forced-Vaccination Forum, http://groups.yahoo.com/group/no-forced-vaccination/join, now just under a thousand advocates strong
* We publish numerous articles and updates on vaccine-related topics in our free Health Freedom eAlerts (to which people can subscribe on our site) where we continually update information on legal and legislative actions designed to remove your health freedom options. Join now: http://drrimatruthreports.com/index.php?page_id=187
* We serve as a clearinghouse for actions and rallys you can take part in like the October 16 No Forced Vaccination Rally in Trenton, NJ (http://drrimatruthreports.com/index.php?p=1166) against the invasive and probably unconstitutional proposed legislation to force home schooled children to comply with the Superintendent of School’s chosen vaccine schedule or be forced back into public schools.
* We support health freedom options for parents and others concerning what goes into their bodies and what happens to them
2. We create and follow through on strong, effective grass roots/net roots and legal actions
* Join the Natural Solutions Foundation’s ground-breaking FTC Citizen’s Petition which you can join here (RALPH, WE NEED AN ACTION ITEM ON THIS- RIMA), a legal action against the Federal Trade Commission AND US Government to compel the FTC to
o prohibit false and misleading advertising or statements that vaccines are safe and effective
o Hold hearings on whether vaccines are, in fact, either safe, or effective, or both
o Force vaccine manufactures, government agencies, doctors, school personnel and others to cease and desist conveying information across state lines which states or implies that vaccines are safe and effective until they are proven to be so
* Urge your legislator to become a co-sponsor of Denis Kucinich’s 3 bill suite to demand safety evaluation and labeling of all GMO foods, including the newly approved “Franken Meats”.
o Click here: http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=25920
* Sign the Tiburon Declaration to let the entire nation know that you are in the majority opposing forced drugging or vaccination. Click here: http://drrimatruthreports.com/index.php?p=460
* Keep Codex tyranny over truthful speech about the relationship about the relationship between food and health out of the US.
o Click here: http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=25929
o and Here:
o http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=26028
o and Here: http://salsa.democracyinaction.org/o/568/t/1134/campaign.jsp?campaign_KEY=1035
* Let your State and Federal Legislators know that you want mercury out of our mouths and out of all health care – NOW!
o Click here: http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=26052
* Support the Child Safety Medication Act to Prevent Compulsory Drugging of Children
http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=18970
And, very important, please Donate to the Natural Solutions Foundation, the largest, and most effective health freedom organization in the world. Our ONLY means of support is the tax deductible support of health freedom advocates like you. Click here (http://drrimatruthreports.com/index.php?page_id=189) to make your donation
Mandatory Vaccination has a long history which is not generally known, but deserves to be understood.
Crunchy Mama wrote the following excellent article posted on Exploring Vaccines. It provides a good overview of the process by which States have come to the point where they are now requiring as many as 78 vaccines by the time a child reaches 15 years of age, starting at birth. The same Hepatitis B vaccine, by the way, that infants are given within 12 hours of birth is literally under indictment in France where the manufacturer has been charged with homicide because of the number of infants who have died following this injection. No such reservations seem to deter the CDC Advisory Committee on Immunization Practices (ACIP) from advising this same, and other highly questionable vaccinations.
Once the ACIP makes its recommendations, States frequently adopt these recommendation and make the requirements mandatory for school entry.
In New Jersey, the issue has been pressed further with a new law now making its way through the legislature which would require home schooled children to meet the same mandatory vaccination schedule approved by the superintendent of schools, not the child’s parents or physician in order to be permitted to continue as a home schooled child.
This unconstitutional and irrational move, from a State with a significant number of vaccine manufacturer headquarters is, we believe, a portent of things to come unless the people of the US make a concerted outcry against this imposition of pharmaceutical profits on personal and religious rights.
The religious exemption is being made more difficult to attain
It is important to note that currently the trend to accept ALL recommendations made by the ACIP is gaining momentum and only vigorous activity by each of us can stop this trend which is damaging our health AND our freedom.
Did you know, by the way, that children are not immunized until they reach the age of 2 years in the UK? Or that vaccinations are widely spaced in Japan? In neither country are children dying of the diseases that supposedly are prevented by vaccination? Perhaps that should suggest that it is hygeine, not vaccination, which prevents these diseases. Perhaps it should also suggest that the Pharmaceutical Industry has a (literally speaking) death grip on US society. Properly used drugs are the leading cause of death in the US, according to the esteemed Journal of the American Medical Association and other journals of equal statue. But we continue to allow, encourage and often require their use. Vaccines, of course, are a particularly contentious and, to my mind, dangerous class of drugs sold into the market place not only through propaganda, but through legislative compulsion.
It is no news that all vaccines are contaminated by dangerous heavy metals including mercury and aluminum as well as fluoride and neurotoxins like formaldehyde, MSG, aspartame, viral particles, including stealth viruses, and cancer causing viruses and stray particles. It is no secret that human (including fetal tissue) materials like DNA are contaminants of viruses, along with dangerous chemicals like Polysorbate 80, linked to infertility.
It is less well know that the adjuvants, which are basically immune irritants, put into vaccines to increase the amount of antibody formation produced by vaccines which, without the adjuvants would not produce enough antibody response to be justified, are themselves serious dangers to health. For example, squalene is more or less harmless if breathed, applied to the skin or swallowed. But as the disastrous Vaccine A experimenets on our troops in the Gulf War have tragically demonstrated, once injected, squalene is the source of immense immune overload and finally, immune collapse in a devastating set of problems lumped together under the term “Gulf War Syndrome”. Most modern vaccines include adjuvants, many of which are secret ingredients, but often include squalene.
Further concern centers around secret ingredients which are not even trade secrets: they are depopulation agents. The World Health Organization (WHO) was recently convicted by the Supreme Court of the Philippines of sterilizing at least 3 million women through the use of a vaccine intentionally contaminated with a human hormone which is necessary for reproduction in women. By including it in vaccines, this hormone causes the body to produce antibodies to it which renders the woman unable to carry a baby although her ability to conceive is not impaired.
According to WHO records, this same depopulation strategy was used in vaccines given to African women starting in 1985 to “eliminate 150 million EXCESS sub Saharan Africans [Emphasis added by me to a quote from WHO documents – REL]. It has been used via a “special” tetanus vaccine series of 5 shots generously given to poor women in South and Central America, Thailand, Africa and elsewhere. The WHO maintains that for the planet to achieve “sustainability” it must have 80-90% fewer people on it than it does today. Its vaccine fertility control task forces for the control of male and female fertility have been operating since 1974, the same year that then-Secretary of State Henry Kissinger prepared Memorandum 200 for then-President Nixon stating that depopulation had to be the US first priority in Foreign Policy, beginning with [note, beginning with- REL] the third world.
As an interesting side note, it is important to consider that a vaccine rendering young women sterile, supposedly for 1 year, is being sold in the US as a birth control option. No one knows if the results are, in fact, induced sterility for one year or not. Life-long sterility could be the result. Time will tell.
This same contamination of vaccines with Human Chorionic Gonadotropin (HCG), the female hormone necessary to carry a baby to term, is intentionally included in the vaccine everypregnant Thai tribal woman is forced to take. Without it, she is told, her baby cannot receive the important identity card. Once she receives the shot from the Department of Health worker, she will inevitably miscarry, no matter how far along the pregnancy is.
Evidence which I find compelling suggests strongly that material designed to drive the immune system, specifically the CD-4 cells, to collapse, opening the way for a host of opportunistic diseases (this induced condition is known by the collective term HIV/AIDS).
The manufacturer of the Hepatitis B vaccine, the same ones given to our children and health care providers, is currently on trial for homicide in France because of the number of deaths caused in infants and others because of known contaminants. Due to the ever-corporate friendly protective nature of the relationship of the US Congress and the FDA, vaccine-injured people in the US cannot hold doctors or manufacturers accountable and cannot sue them for the damages incurred. On a positive note, that wall of non-protection has been breeched in a Georgia case in which a Federal judge has ruled that parents may sue a vaccine manufacturer for damage to their child.
This landmark case may open a door which regulation and legislation has shut for Americans, as the consent by the CDC in the Vaccine Injury Special Court system that a 9 year old autistic girl was vaccine injured because of a supposedly rare mitochondrial disorder and is thus entitled to compensation for her care may open a small doorway for vaccine injured children.
The bigger door, however, is to make sure that no one IS vaccine injured or, if they chose to run the risk of such injuries, that they will be free to do so in the full knowledge of the risks incurred by submitting to vaccination.
Currently, the US has announced its determination to vaccinate very man, woman and child in the US with an Avian Flu vaccine made in China by Sanofi-Pasteur and loaded into individual dose syringes in Pennsylvania. This vaccine was approved by the FDA in the complete absence of any formal clinical trials (although apparently informal ones have been conducted in Poland where the impact of the vaccine on the over 300 vagrants vaccinated include 11 immediate deaths and hundreds of reactions so severe that the 2 physicians and 4 nurses involved in the “trial” are now accused of homicide. The Minister of Health of Poland has said that none of the accused should ever be permitted to practice medicine or nursing again. This same vaccine is, according to our information, the stuff waiting for the compliant arms of “every man, woman and child in the United States”.
Further information suggests that not only the Avian Flu virus itself, but the very vaccines designed to “protect” us against it (although the science behind ANY vaccine protecting us from anything is worse than questionable) has also been weaponized.
Two biochemistry/microbiology researchers were brutally tortured and murdered on June 29,208 in London, England. Their computer was stolen shortly before their murder. These researchers were, according to information released recently, murdered by a British-Mossad assassination team now in custody in the UK. The researchers had uncovered information leading to the conclusion that not only was the Avian Flu virus itself weaponized with genetic material from the 1918 pandemic “Spanish Flu” (which was not Spanish at all, but created in the US as the first, and most successful Bio Weapon of all time on orders of then-President Teddy Roosevelt and injected into US Soldiers in Kansas before they were sent to Spain for “training” and exposure to mutation-inducing poison gases)but the vaccines supposedly being created to protect the population from the approaching pandemic Avian Flu had also been weaponized to produce a deadly disease upon injection.
Their horrific murders and the subsequent apprehension of their professional killers was covered by the European press, but totally ignored by all US media. The story of their discoveries was also totally neglected by the US media.
The Natural Solutions Foundation’s press release was censored by the media outlet we attempted to use to bring this attention to the light of day and request substantiation of this vitally important information by the media outlet which published it in September, 2008.
Mandatory vaccination for mumps was imposed on college students in Maine last December 11, 2007. Students who were not vaccinated or chose to refuse vaccination were locked out of their dormitories, dining halls, libraries, student unions and classrooms when their key cards were inactivated. This happened on the same day that Health Canada withdrew approval for the same vaccine for use in children and adults because of its dangers. Students, whose tuition, room and board were already paid for, were denied access to instruction and shelter, food and resources in the winter time without notice.
Mandatory vaccination is now being recommended for college students, especially those in dorm, even though, as the article making this recommendation states, last year’s flu vaccine did not “cover” one of two viruses causing the flu. This year’s flu vaccine will supposedly contain 4 viruses in an attempt to avoid last year’s embarrassing failure by the CCDC and World Health Organization (WHO) to “guess” right in the spring before the flu season hit. Each year, these organizations decide what the offending virus is likely to be in the next flu season and authorize vaccines against those viruses which are then recommended (or mandated)as the “flu shot”. Last year, as often happens, the guess was wrong and the CDC announced that the vaccine was ineffective from 40-60% of the time.
Given that 94% of the flu vaccine available contained thimerisol (50% mercury by weight)as well as the usual toxins, and whatever else the vials might be hiding, and that both children and adults are susceptible to the toxic impact of these biological and chemical components, this tetravalent vaccination does not suggest any more safety than the previous ones, including the disastrous and deadly Swine Flu vaccine) offer.
New Jersey made headlines last November by announcing that it would require mandatory flu vaccination for all children in the state from age 6 months (2 shots in the first year) to age 18 plus meningococcus and Hepatitis B shots for all children in the state at various times in their school career.
Now this state, home to so many major pharmaceutical companies, has taken the mandatory vaccination thrust a step farther: all children, whether enrolled in school or home schooled, MUST receive the vaccines approved by the Superintendent of Schools for the child’s home district or be refused permission to stay in a home schooled environment.
Despite the total global absence of a pandemic strain of Avian Flu and despite excellent evidence that non toxic strategies like nanosilver ingestion and hygiene measures are sufficient to kill any Avian Flu virus yet identified, the thrust is toward untested, potentially very dangerous, and scientifically absurd vaccinations. These vaccines, however, carry a hefty price tag: the Sanofi-Pasteur vaccine, approved by the FDA on an “emergency basis” for a disease that does not exist, and slated for use in every person in the US, and approved in the absence of any formal trials, was purchased by the US Government for the hefty price of $15 per dose, or $1.5 billion dollars for 100 million doses. This vaccine shipment, the first of several if all Americans will receive at least one dose, gives the US government a tight exclusive on the vaccine preventing price cutting or competition: in its approval documentation, the fact that the vaccine cannot be sold to any agency or customer other than the US Government is stipulated.
This stipulation means that the ingredients are not listed, do not have to be listed, may not be listed on the package insert or elsewhere.
Americans were notified on July 23, 2008 by the FDA and on July 24, 2008 by the Department of Homeland Security, that the intention of the US Government is to vaccinate every person in the US with this vaccine “starting with those who want it”. Americans are well aware that Patriot Act I and II, BioShield I and II and BARDA all make mandatory vaccination a requirement to avoid involuntary internment and quarantine.
They are also well aware that hundreds of thousands of plastic coffins have been purchased by the US Government and are sitting in depots, including the one famously photographed in Georgia.
American know that every state in the country has passed a version of the Emergency Medical Powers Act which makes refusing treatment, especially vaccination, once a “Pandemic” has been declared by the governor of the state, a felony which, as such, can be punished by incarceration or internment.
They are well informed about the fact that the US Government is reported to have purchased at least one large tract of land in upstate New York for a mass burial site and that the UK has announced mass burial plans as well since cremation would, according to the estimates of the British Parliament, run up to 17 weeks behind deaths despite increased crematoria capacity building recently undertaken.
All this for a disease that does not yet exist.
Americans are also aware that US troops have been moved into place to control civil disruption, subdue unruly persons relocate persons as necessary in a permanent domestic duty deployment which began October 1, 2008. The 1st Battle Group of the 3rd Infantry has been placed under the permanent command of NorthCom, the Northern Command of the US Army. NorthCom signed a much hearalded agreement with the Canadian Military to allow Canadian troops access to US territory for the same reasons and US troops have been operating in Canada performing domestic duties since April, 2007.
This, of course, follows the integration of the US FDA, Canadian HealthCanada and Mexican Department of Health under the Trilateral Cooperation Charter in 2003, erasing further the sovereign powers and status of the United States.
So Americans are well aware of the vaccine threats lurking. They remember well the November, 2007 atrocity in which Prince George’s County imposed vaccination under the amused and watchful eye of a judge (who remarked that the crying children were “kind of cute”) on threat of imprisonment and fines for parents of unvaccinated children and re vaccinated 1100 children whose records it admitted it had lost but who were fully vaccinated. They also remember the interviews granted by State’s Attorney Glen Ivey, father of young children, who admitted that he would not allow his own children to receive the vaccines which were being administered under police and attack dog guard in the Court House that tragic November Saturday. Maryland is among the states which allow parents to file an exemption if they do not want their children to receive the vaccines offered. These parents, mostly poor, black (like Attorney Ivey) and uneducated, from the one of the poorest school districts in the nation, were not told of their option to refuse these vaccinations.
The Natural Solutions Foundation asks you to take effective and vigorous action by notifying your state and federal legislators that these compulsory vaccination precedents are not acceptable to you. Please take a moment to sign the Tiburon Declaration, which takes issue with compulsory drugging, including vaccination, and which will be presented to all US legislators when we have amassed enough signatures. Then please take another moment to take each of the action steps listed above if you have not already done so, to raise the voice of the net roots loud and clear so that legislators understand that they are playing with your health freedom and that you do not like that and will not allow that to continue.
Let’s stop this right now!
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
www.NaturalSolutionsMedia.tv
How School Vaccine Mandates Came About
In 1809, the first state law mandating vaccination was enacted in Massachusetts. By 1855, Massachusetts became the first state to enact a school vaccination requirement for Smallpox. By the twentieth century, roughly half of the states had enacted vaccine mandates for children before they could enter school; however, they were not strictly enforced. The Diphtheria vaccine was introduced in the 1920’s, but only a few states made the Diphtheria vaccine compulsory for two decades. By the early 1950’s, with the licensure of the Diphtheria and Tetanus vaccines, state and local health departments began more aggressive vaccination programs. When the Salk Polio vaccine was licensed in 1955, only a few states passed laws that mandated it for school entry. The polio vaccine also led to federal funding of state and local vaccine programs. In 1962, the Vaccination Assistance Act established a federally coordinated program that would supply funds for the purchase and administration of childhood vaccines. By 1963, several vaccines were mandated, but there was no enforcement by all states. The New York City health commissioner opposed making the Polio vaccine mandatory in 1965.
Compulsory vaccination made some radical changes by the late 1960’s and 1970’s. In 1970 a nationwide rubella vaccine campaign was launched. It was recommended by the Department of Health for all 11-13 year old girls. Then the CDC moved on and began leading a nationwide effort to eradicate Measles. In 1968, only a half the states required one or more vaccines for school entry. By the early 1970’s, the Measles Initiative program was started. By 1976-77, health officials strictly enforced the vaccine mandate for Measles under the Childhood immunization Initiative. Its purpose was to raise vaccination coverage in children to 90% by 1979. The largest component of this initiative was to enact and enforce school vaccination mandates.
By 1981, all fifty states mandated Measles vaccine along with all others for school entry. Nearly all states had school vaccination mandates covering Kindergarten through 12th grade levels, and mandates for licensed preschools. State mandated vaccine laws specified which vaccines would be required and the number of doses. Some states authorized the public health boards to designate which vaccines and doses would be required. States were not uniform in what vaccines they require, or how many doses. This still holds true today. In 1980, the state of Wisconsin passed the No-immunization-No School law and was enforced by March 1981. Other states soon followed.
In 1998–1999, all but four states (Louisiana, Michigan, South Carolina, and West Virginia) enacted mandates which covered Kindergarten through 12th grade. In 48 states, with the exception of Iowa and West Virginia, daycare mandates and Head Start program mandates were enacted. Thirty states mandated some requirements for college entrance. School vaccine mandates included:
All 50 states required: Diphtheria toxoid, Polio, Measles and Rubella vaccines
49 states required: Tetanus toxoid
46 states required: Mumps
44 states required: Pertussis
28 states required: Hepatitis B
During the late 1980’s and early 1990’s, state vaccine laws were tightened to make religious and philosophical exemptions harder to obtain. By the end of the 1990’s, the trend was reversed. Religious and Philosophical exemptions were made less restrictive through rewriting exemption clauses.
The Task Force on Community Preventive Services is an independent body carrying out evidence-based reviews of the literature to assess the claims that preventive interventions directed to populations are effective. One of the 17 interventions reviewed for vaccine-preventable diseases was mandatory vaccination requirements. The Task Force found that sufficient evidence existed to demonstrate the effectiveness of these requirements in increasing vaccine coverage, thereby reducing disease incidence, and so recommended their use.
U.S. Congress passed the National Childhood Vaccine Injury Act in 1986 and the Vaccine Compensation Amendments in 1987 and 1995. The NCVIA establishes a compensation system for people who may be injured by routine vaccinations. The National Childhood Vaccine Injury Act of 1986, Public Law 99-660, was signed by President Reagan in November 1986, however, it did not contain a funding mechanism to enable the compensation system to operate. In 1987, Congress passed amendments to the law and developed a plan to fund the system, which comes from a surcharge on each mandatory vaccine. The main purpose of the law was to create safety provisions for the administration of vaccines to help prevent future vaccine injuries, to promote the improvement of existing vaccines and develop safer vaccines. Another element was to create a no-fault compensation system alternative to suing vaccine manufacturers and physicians on behalf of injured or deceased people from reactions to mandated vaccines. Children and/or adults injured or killed from these vaccines are divided into two categories; those who were damaged or killed before October 1, 1988 and those who were damaged or killed after that date. In 1990, the FDA and the CDC developed the Vaccine Adverse Event Reporting System (VAERS), which allows public and private physicians to use one standard reporting form to report reactions.
http://explorevaccines.wordpress.com/2008/10/08/vaccine-state-mandates/#comment-41
NOTICE: A Rally to protest Assembly Bill 3123 will take place in Trenton NJ on October 16, 2008 Here is the information:
1. The rally begins at Noon at The State House, 125 West State Street, Trenton. Directions: http://tinyurl.com/4c34r7
2. For parking, go to http://www.trenton-downtown.com/parkdowntown/. Street parking is available but regular rules and fines apply. Free parking is available behind the State House on Memorial Drive and at 225 West State Street.
3. The best way to get easy, free parking at the rally is to spread the word and tell people to attend. Once we exceed 500 participants (we are nearly there so keep spreading the word), the city will close the streets and designate parking.
4. We will rally, rain or shine.
5. The rally is scheduled to end by 2:00 pm. We may run a few minutes late. Our permit expires at 3:00pm.
6. If you have a Raggedy Ann doll or can get hold of one, bring it. You’ll hear her story at the rally.
7. Bring red, white and blue helium filled balloons.
Thanks, and let people in the New Jersey area know about this!
Vaccine Tyranny Grows More Legs and Teeth In New Jersey
New Jersey is home to a large number of very wealthy and powerful pharmaceutical companies and it is clear that neither the governor nor the legislators of that state are willing to disappoint them in their quest for unlimited vaccination access to every man, woman and child in their reach.
Forget the fact that New Jersey’s autistic population already reaches astounding levels:
“Researchers in 14 states conducted the autism monitoring activities in demographically representative sections of their states, under the umbrella of a CDC-sponsored network called the Autism and Developmental Disabilities Monitoring Network, or ADDM. Walter Zahorodny, Ph.D., an assistant professor of pediatrics and psychiatry at the UMDNJ-New Jersey Medical School, was the lead researcher on the New Jersey portion of the ADDM network investigation.
The New Jersey monitoring covered Essex, Hudson, Union and Ocean counties. The autism spectrum disorder prevalence rates identified in those areas of New Jersey were higher than in other ADDM-surveyed states – 9.9 cases per 1,000 8-year-olds in 2000, and 10.6 cases per 1,000 8-year-olds in 2002. According to the new findings, New Jersey’s autism rate is the highest of the 14 states in the ADDM network.”
http://www.umdnj.edu/about/news_events/releases/07/r020807_CDCReleases_StudyofAutismRates.htm
Forget the fact that 94% of the available pediatric vaccination doses still contain mercury. Forget the fact that flu vaccines cause the symptoms of flu as side effects of the vaccination itself. Forget the fact that most epidemics occurs in fully vaccinated populations. Forget the fact that vaccines carry dangers far beyond mercury, aluminum hydroxide, formaldehyde, fluoride, MSG, aspartame, Polysorbate 80 (associated with infertility). Forget the fact that vaccines are routinely contaminated, according to the FDA and CDC, with stealth viruses, parts of human, animal and virus genetic materials, carcinogenic viruses and other potentially lethal debris.
Forget about the fact that parental rights should determine if a child is vaccinated. Forget about the fact that the State of New Jersey has decided that religious exemptions can only be granted if the child has NEVER had a vaccination in his life because they have decreed an “all or nothing” policy whose logic I have not yet been able to disect in order to make sense of it.
Just remember that the State of New Jersey knows that parents sometimes feel so strongly about their dangerous invasive vaccination policies that they will homeschool their children rather than subject them to the dangers, or religiously unacceptable, vaccines decried by the State.
And then, again, sometimes parents homeschool their children for completely different reasons but do not believe in, see the necesity for, or want vaccinations for their children.
Well, the State has other ideas. Not only must the curriculum meet the needs and whims of the Superintendent of the home district of the child, but the vaccination schedule that the Superintendent enforces (I’m sorry, I thought they were superintendents of education, not vaccination policy – I guess I got that wrong). Otherwise, the child is immediately sucked back into the school system – complete with vaccinations.
Consider what that means to a vaccine injured child. Consider what that means to freedom. Consider what that says about the onrush of the police state which owns your body and your child’s.
Ralph Fucetola, attorney and trustee of the Natural Solutions Foundation has this to say about the attack on home schoolers, health and freedom in his Vitaminlawyer blog on the subject:
NJ May Mandate Vaccines for Home schooled Children!
That’s right. NJ, even as we are fighting the Dietitian’s Monopoly Bill and seeking to secure protection from dangerous, mandated vaccinations, is planning another vaccine assault on our children.
Assembly Bill A3123, the anti-homeschooling bill introduced on September 28, 2008, among other evil provisions, would enact:
“1. Prior to the establishment of a home education program and annually thereafter… a parent or guardian shall submit to the superintendent of the resident school district a notarized letter registering his child in a home education program. The letter shall include … e. evidence that each student being registered has been immunized in accordance with the provisions of the State Sanitary Code…”
http://www.njleg.state.nj.us/2008/Bills/A3500/3123_I1.HTM
Privacy? Parental Rights? Religious Rights? Protection of our Children from Assault by the Uninsurable Risk of Vaccination… the Trenton Thugs continue the attack, so we must continue to defend our families!
Health Freedom is at risk yet again, and yet again, the attacks on freedom of choice are attacks on the lives of our loved ones.
The system is sick it needs a really big dose of freedom to recover!
http://vitaminlawyerhealthfreedom.blogspot.com/
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
www.NaturalSolutionsFoundation.org