In 1976, the barely “tested” vaccine formulation had no Thimerosal (ethyl mercury), but the one they gave the public was Thimerosal-preserved! Before the vaccination program was stopped, 46 million people had been vaccinated; 4,000 people sued for damages from side effects, including neurological damage such as paralytic Guillian Barré syndrome or death. See youtube.com/watch?v=5lcJt4jX1Vo
This time we have been told most doses of these flu shots will be in multi-dose vials (which are preserved with Thimerosal (49.5 percent mercury by weight, a compound whose safety has never been proven as required by law). However, unlike the last time:
(a)MedImmune is preparing 25 million live-influenza doses to ensure there will be 25+ million swine-flu cases.
(b) There will be several inactivated-influenza vaccine suppliers who will produce vaccines with differing adverse-effect profiles, so it will be more difficult to prove the vaccine was the cause. Unadjuvanted vaccines (vaccines without chemical immune “helpers”) will be tested, but many may get an adjuvanted shot. See dailypaul.com/node/103773
(c) There will be no guaranteed compensation for anyone harmed—not even under the NVICP—because these vaccines will not be adequately tested for safety, much less for effectiveness. A few clinical trials for “efficacy and dose” started in late July (see clinicaltrials.gov/ct2/results?term=swine+flu), but all without proper safety testing (where a placebo containing only buffered sterile saline is used) because of the “safety” (a lie) of the similar human influenza vaccines given from 1950s to the present. These swine-flu vaccines will be given under a health emergency (“Pandemic Alert”) scenario with apparently no FDA-regulation-compliant approval. See thenhf.com/newsflash_57.htm
(d) Like all vaccines, the long-term mercury-poisoning and immune-system harms will not even be looked for. Most “trials” will only look for adverse effects for 21 days.
(e) The current scenario calls for all to get the recommended annual flu vaccines plus two doses of the swine-flu vaccines—three shots in all.
(f) They will start with pregnant women whose unborn children cannot complain. Each mercury-preserved flu shot a pregnant woman gets during pregnancy will further increase her proven one-mercury-dose risk of having a child with a serious birth defect such as cleft palate, microcephaly (small head; mental retardation), and pyloric stenosis (malfunction of stomach emptying and gastrointestinal problems). For details concerning the risks, see mercury-freedrugs.org/docs/20090709_Drft_ReviewOfFDAsThimerosalinVaccinesQAb.pdf pp 52–53.
Children, who are less able to resist and much more likely to be harmed, will be among the first vaccinated; and finally the adults will be vaccinated unless the harm has, as in 1976, become so widespread that they refuse en mass to be vaccinated.
Moreover, given a mortality rate that appears to be on the order of 1 in 100,000 to 1 in 1,000,000 in “healthy” people exposed to the swine flu itself, the vaccines will probably, as they did in 1976:
(a) Harm hundreds of times more than those who are not inoculated but get and recover from swine flu, and
(b) Kill 10 times as many as would die from the flu-related effects from swine flu. (In 1976, only one unvaccinated man died after being on a forced march while sick, whereas 25 died from being given the swine-flu vaccine.)
With respect to the live-virus swine flu inoculation, reading the FluMist insert clearly indicates that the person inoculated is infected with a supposedly self-limiting live virus and can infect others.
If, as the government is claiming, the bioengineered swine-flu virus is more easily spread, then clearly, if you infect 25,000,000 with this bioengineered live swine-flu variant, you will have more than 25,000,000 additional swine-flu infections.
When this live swine-flu virus undergoes reassortment with the live A/H1N1 vaccine viruses, the worst-case scenario would be that the swine-flu virus’ infectivity would increase from the “1 percent” level to the “30-plus percent” level and transmissibility increase from the “less than10 percent” level to “more than 50 percent”—where inoculating 25 million might produce 100 million cases of “influenza”—but “no one” knows.
At a minimum, against an annual background level of 30 to 50 million cases of human influenza, inoculating 25 million with live swine flu vaccine will increase the number of cases to the 55 to 75+ million level, not counting the cases from the annual FluMist.
Given the propaganda, governmental pressure, the expenditure of billions, and the need to damage more fetuses, pregnant women, children, and adults to increase the supply of the chronically ill required to support our bloated health care system and the pharmaceutical industry, a simple “No thanks!” will, be met with threats. Moreover, health care workers, who try to say “No thanks!” for the current ineffective human flu vaccines, already risk loss of their jobs.
Only a mass refusal has any chance—especially given the recent laws, construction of detention centers, and the training of American troops to assist in managing the “dissidents” as well as the declaration of a “Health Emergency” when there is not one.
Too bad the American people will not stand up and, as a group, simply say “HELL NO”!
Dr. King is the founder of FAME Systems, a consultancy for pharmaceutics, quality systems, and regulatory compliance. He is also the science advisor for and secretary of CoMeD, Inc., a not-for-profit 501c 3 organization whose goals include stopping all use of mercury in medicine.
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