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Universal Declaration of Resistance to Mandatory Vaccinations 062109

Universal Declaration of Resistance to Mandatory Vaccinations 062109

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Published by wire-of-Information
The Universal Declaration of Resistance to Mandatory Vaccinations
The Universal Declaration of Resistance to Mandatory Vaccinations

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Published by: wire-of-Information on Sep 02, 2009
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05/26/2012

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A UNIVERSAL DECLARATION OF RESISTANCE TO MANDATORYVACCINATIONSWe the undersigned, as Freemen & Freewomen, do not recognize the authorityof The World Health Organization (WHO) to mandate general forcedvaccinations. Our bodies are sovereign territory and subject to our exclusiveself-determination. Any attempted violation of this trust must be construed as abreach of said basic right. We are thus holding our elected Governmentsaccountable in this defense with an issuance of notice: a preemptive ClassAction Lawsuit to be served in the event our inalienable rights to choose areforsaken.
WORLD HEALTH ORGANIZATION checklist for influenza pandemic preparednessplanning: Section 1.5.1 Legal and ethical issues -'During a pandemic, it may be necessary to overrule existing legislation or(individual) human rights. Examples are the enforcement of quarantine(overruling individual freedom of movement), use of privately owned buildings forhospitals, off-license use of drugs, compulsory vaccination or implementation ofemergency shifts in essential services. These decisions need a legal framework toensure transparent assessment and justification of the measures that are beingconsidered, and to ensure coherence with international legislation (InternationalHealth Regulations).http://www.who.int/csr/resources/publications/influenza/FluCheck6web.pdf 
There is no forensic evidence showing the H1N1 virus as the direct cause ofdeath in those who have died after contracting the virus (144 to date). Themajority of deaths are caused by pre-existing complications and auto-immunedeficiencies. Countries with low quality of health have the greatest number offatal cases. Based on the Center for Disease Control's own guidelines H1N1related symptoms are virtually indistinguishable from those of the commonseasonal flu, and severity is comparable to mild seasonal flu,
'The symptoms of this new H1N1 flu virus in people are similar to the symptoms ofseasonal flu and include fever, cough, sore throat, runny or stuffy nose, bodyaches, headache, chills and fatigue. A significant number of people who have beeninfected with this new H1N1 virus also have reported diarrhea and vomiting. Thehigh risk groups for novel H1N1 flu are not known at this time but it's possible thatthey may be the same as for seasonal influenza. People at higher risk of seriouscomplications from seasonal flu include people age 65 years and older, childrenyounger than 5 years old, pregnant women, people of any age with chronicmedical conditions (such as asthma, diabetes, or heart disease), and people whoare immunosuppressed (e.g., taking immunosuppressive medications, infected
 
with HIV).'http://www.cdc.gov/h1n1flu/sick.htm 
GlaxoSmithKline are the major Pharmaceutical developers behind the H5N1Avian Flu vaccine. Given the fact the new H1N1 strain is an Avian/Swine/ Human hybrid it is likely this component will be used as part of the 3 shotregime,
'GSK's proprietary adjuvant is called ASO4. It contains alum and MPL. MPL standsfor monophosphoryl lipid A. The U.S. Army's proprietary (unlicensed) adjuvantdeveloped prior to the first Gulf War for use in a second generation anthrax vaccinewas called Tri-Mix or Triple Mix. Tri-Mix contained MPL (monophosphoryl lipid A)and squalene. After the war, Army scientists considered MPL to be too toxic, sothey began working with Chiron Corporation of Emeryville, CA to develop anadjuvant that contained squalene and water only ... on the assumption thatadjuvant toxicity with Tri-Mix was due to MPL. This assumption also provedincorrect. There are more than two dozen animal studies that generated datademonstrating squalene's ability to induce autoimmunity; and there is disputedevidence that nanodoses of squalene in anthrax vaccine sickened countlessmilitary personnel who received squalene-tainted vaccine during AVIP. MPL wasalso a component of the Ribi Adjuvant System. The Ribi Adjuvant System, or RAS,is a derivative of Tri-Mix, which is approved for use in animals only. There is noexisting data showing whether MPL elicits an immune response specific to it. IfMPL is immunogenic, it raises the possibility of a dangerous "cross reaction." Thehuman body is full of lipids. Antibodies and immune cells responding to MPL mightalso respond to other lipids in the body, thus breaking tolerance for endogenouslipids (those native to the human body) and initiating autoimmunity.' GaryMatsumoto - Journalist/Author of Vaccine Ahttp://www.whale.to/vaccine/secret_adjuvant.html 
The risk of a widespread outbreak of Gulf War Syndrome amongst the generalpopulation is inevitable - assuming the same H5N1 squaline adjuvant is utilizedon H1N1 (Adjuvants are pharmacological or immunological agents that modifythe effect of other agents). Further the vaccine administered produces littleantibody response. Therefore it requires 12 times the normal dose in order tobe 'effective'. Such a gamble where our lives are concerned is non-negotiable.Pharmaceutical Companies (Novartis among others) stand to reap a hugewindfall during such a crisis. We are not willing to wager our safety for Industryprofits under any conditions,
'The swine flu outbreak is going to benefit one of the most prolific and successful
 
venture capital firms in the United States: Kleiner, Perkins, Caufield & Byers. Shareprices have already risen for two of eight public traded companies in the firm'sportfolio of Pandemic and Bio Defense investments. BioCryst, up more than 26percent, to $2.21 per share, and Novavax, maker of viral vaccines, escalated 75percent to $1.42 per share on the first announcement of the swine flu outbreak inMexico.'http://drtenpenny.com/swine_flu.aspx 
The lack of sufficient testing on this experimental vaccine raises manyconcerns. There is no criteria on its efficacy or valid statistics to speak of,
'Novavax uses genetic information and "recombinant, virus-like particle technology"to rapidly engineer a vaccine. Its technology has only been through Phase IIclinical trials but might be released prematurely. Novavax's CEO, Rahul Singhviannounced Friday, "There is an emergency authorization avenue that is availablethat would allow us to use the vaccine in an emergency without further testing." TheDivision-E provisions would protect the company from all liability.'http://drtenpenny.com/swine_flu.aspx 
H1N1 is an entirely unique strain, never seen before with all the hallmarks of alaboratory-produced designer virus,
'Author of Emerging Viruses: AIDS And Ebola: Nature, Accident or Intentional?,Horowitz says the swine-bird-human flu strain, reported to be found first in Mexicoin late-March 2009, could have only come from Dr James S. Robertson and hiscolleagues in association with the US Centre for Disease Control and vaccinemanufacturer Novavax, Inc, which was ready to profit from the release he says.Nobody else takes H5N1 Asian-flu infected chickens, takes them to Europe,extracts their DNA, combines their proteins with H1N1 viruses from the 1918Spanish flu isolate, additionally mixes in some swine-flu genes from pigs, thenreverse engineers them to infect humans, he said.http://uncensored.co.nz/2009/04/30/dr-horowitz-mexicanswine-flu-made-in-lab/  
During the 1976 Swine scare the Swine Flu vaccine itself killed hundreds &sickened countless others,
'Only young Lewis (19-year-old Pvt. David Lewis of Ashley Falls, Mass) died fromthe swine flu itself in 1976. But as the critics are quick to point out, hundreds ofAmericans were killed or seriously injured by the inoculation the government gavethem to stave off the virus.'

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