[back] Medical study ploys Placebos
“They all only use benign placebos – we use the safest most pure vaccines as
a placebo."---David Salisbury
The Arnica Network)
"We have not studied vaccinated vs. unvaccinated."--- Coleen A. Boyle, Ph.D., Director, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention responds to Congressman Bill Posey during a November 2012 Congressional hearing.
[There has never been (that anyone has found) any vaccine study done using 100% unvaccinated children as controls. They know it would show up their vaccine to be unsafe and/or useless, and that Unvaccinated children are healthier as Dan Olmsted found in the Amish. The cover story: it would be unethical to leave a control group of children unprotected against vaccine-preventable disease (Orac quote). There are tens of thousands of unvaccinated kids around to study.]
See: Healthy trial babies only Inadequate safety studies Leicester Placebos
See: DPT Mouse tests Mouse toxicity test Kendrick mouse test Hist test
[2012 Oct] Vaccine Research Conflicts of Interest: Vaxxed & Unvaxxed Kids Not Compared Conflicts of interest are rampant in vaccine research. How and why they exist are the topic of a journal article reviewed here. This is why research that could prove that vaccines are safe hasn’t been done.
[2010 Nov] A VACCINE CHALLENGE TO MAINSTREAM RESEARCHERS---HAS A TRUE CONTROLLED STUDY ON A VACCINE EVER BEEN DONE? By JON RAPPOPORT Here is my assertion: this kind of controlled study on vaccines has never been done. It has never been done for any vaccine anywhere, at any time. And I have no reason to believe it will ever be done.
[Swine flu vax 2009 Aug] Injecting one thing for testing and then adding adjuvant later
 SEEKING THE TRUTH ABOUT THE NEVER-VACCINATED by Sandy Gottstein
[2009 Feb] Unvaccinated Children Madness By J.B. Handley One final point: the mainstream will never do a study of unvaccinated kids. They already fear what it will show, and the results for them would likely be cataclysmic. Their best bet is to invent reasons the study can't be done.
"One of the flaws in studies of vaccines is that there are no true placebo groups. The vaccine is tested in one group of immunized children and is compared to another group of immunized children."--Peter Baratosy
Marcella Piper-Terry shared: "You know how we've been told all those serious adverse reactions to Gardasil are "coincidence" and would have happened anyway? B.S. Merck used the aluminum adjuvant as the "control" in their clinical trials. There was no placebo. Of 7 clinical trials, only one used a placebo (saline solution) and the number of subjects was 594. In comparison, 15,706 subjects received Gardasil and 13, 023 subjects were injected with the aluminum adjuvant. They compared the number of serious adverse events between the Gardasil group ("experimental") and the adjuvant group ("control"). Not surprisingly, there was no significant difference between the number or severity of adverse events between the groups. That's because aluminum is a neuro-immune toxin and subjects who received the aluminum "control" were disabled, had seizures, developed autoimmune disorders and died at nearly identical rates to those who received the Gardasil vaccine. The serious adverse events are being caused by the aluminum. They are not "coincidence" and they would not have occurred naturally. Take home message: There is no safety data for Gardasil - and this is the status quo for vaccine manufacturers. Do you REALLY think they care about your health? Hint: the 3-shot series is nearly $400. Per person. No wonder they want to vaccinate little boys and infants, too. Just say NO."
Anyone analyzing the “vaccine safety studies” done by
vaccine makers and vaccine proponents can see that they were purposely designed
to show safety by omitting people in the study who truly reflected the
population being vaccinated and who were, by all standards of science, at risk
of harm by the vaccines.
They do studies that use as placebo controls people injected with a vaccine adjuvant. Placebos are supposed to be completely inert. The evidence shows that the greatest danger from vaccines is from the vaccine adjuvant — so, how can they use adjuvant-injected people as controls? Yet, all of their studies used such vaccinated controls — this is blatantly manipulated, and they know it.
The studies that are quoted endlessly by these elite members of academia and government agencies and used to close the door on the vaccine connection to neurodevelopmental problems are purposefully designed so as to suggest no link between vaccines and any complication.
This falsified research is protected by academia, the media, and government agencies. Yet, they have the audacity to stand in judgment of Wakefield. This is not to say that Wakefield should be free of scrutiny — all researchers should be carefully scrutinized for bias. [2011 Jan] Big Pharma Vilified Researcher for Threatening Vaccine Program By Russell L. Blaylock, M.D.
Allowing other than sterile saline to be used as the placebo
in short-term vaccine adverse-reaction studies to suppress
the relative incidence rates to the point that these relative
adverse-event rates show “no statistically significant” increase
over the “placebo” (that, in some cases, has been allowed
to be an experimental vaccine or the vaccine formulation
without the biological antigens).
Permitting vaccine safety studies to be restricted to a few days or, at most, a few of months even though some severe adverse outcomes do not begin to emerge until several years after vaccination (e.g., childhood MS 4 years after vaccination).
Consenting to reductions in the size and number of persons in the phase-III clinical trials that not only reduce the vaccine makers costs but also reduce the risk that the study will find the rare but deadly adverse effects that a vaccine may have.
Allowing surrogate endpoints (e.g., the reactivity of the patient’s blood to animal anti-sera) for specific antibodies to be used to assess vaccine efficacy instead of requiring comprehensive testing to establish both general and specific immunity in those vaccinated that is comparable to the immunity found in those who have had the disease.
Recommending widespread use of new vaccines long before the long-term (at least 10-year) outcomes can be assessed in the trial population, and
Licensing vaccines and recommending their “universal” use in populations that have near-zero risk of contracting a disease (e.g., the hepatitis B vaccine in young children or the HPV vaccine in non-sexually-active children) or where the clinical cases of the disease occur at low rate and are virtually absent in most demographic segments of U.S. population (e.g., the rotavirus vaccine). Key realities about autism, vaccines, vaccine-injury compensation, Thimerosal, and autism-related research----Gary S. Goldman, Ph.D & P.G. King PhD