Time to Unite in Dissent

The global spotlight is on the rushed development and rollout of experimental COVID-19 vaccines, and it is shocking to see the Washington State Department of Health and the local media begin major campaigns to counter what they are calling “vaccine hesitancy” and what any rational person is calling “medical due diligence and warranted caution.”

It borders on criminal, and it is certainly unethical, to use the power of the state and taxpayer dollars, and the extensive reach of major media, to coerce and compel and even shame those who are asking critical questions about liability-free experimental vaccine products.

The hype being spun is not based on trial data but on information from press releases put out by the companies, which sent their stock soaring, and their officers cashing in their stock to haul in massive profits. And all of this mess can be greatly attributed to the flawed and inappropriately used PCR tests.

We need every single person in this state to read and share the below linked documents that have been submitted to the appropriate agencies. These are by experts in their fields, and they reveal disturbing problems with the coming vaccines and the PCR testing that is driving what can only be called a “casedemic.” Investigations are needed now.

It is likely impossible to completely stop the massive, global, billion-dollar force pushing the vaccines onto the public, but we can simply all say no. We can say —


We dissent the use of flawed PCR tests, the experimental vaccination rollout, the masking policies, the shut-down policies, the restrictive policies that are causing untold collateral damage. We dissent the misdiagnosis caused by PCR tests leading to inappropriate medical care. We dissent the state ignoring existing treatments: refusal to support and disseminate existing treatments is yet another potentially criminal and certainly unethical act of our state’s response.


An international consortium of life-science scientists performed an extensive review of the pivotal study, referred to as the Corman-Drosten paper, that led to the global use of the RT-PCR tests to detect SARS-CoV-2 and diagnose “cases.” They found 10 major scientific flaws at the molecular and methodological levels.

“In light of our re-examination of the test protocol to identify SARS-CoV-2 described in the Corman-Drosten paper we have identified concerning errors and inherent fallacies which render the SARS-CoV-2 PCR test useless.”

CLICK HERE TO READ OR DOWNLOAD THE Report https://cormandrostenreview.com/report/

EXPERTS SAY: Clinical Trials Do Not Have Valid Endpoints

Dr. Sin Hang Lee has filed a citizen petition with the FDA to pause the Pfizer’s Phase III trial of their COVID-19 experimental mRNA vaccine BNT162—and all other vaccines for which PCR results are the primary evidence of infection—until its study design is amended to accurately assess efficacy. Dr. Lee explains his concerns at length in his filing.

“Furthermore, if the vaccine is approved without an appropriate and accurate review of efficacy, then any potential acceptance or mandate of these vaccines is likely to be based on inaccurate evidence regarding the vaccine, namely that it will stop transmission of the virus from the vaccine recipient to others and/or that it will reduce severe COVID-19 disease and deaths. The Pfizer trial protocol is currently not designed to determine whether either of those objectives can be met; and even if it was, if cases cannot be reliably identified, neither objective could be reliably met.”

Click here to Read or Download the Filing: Stay-Pfizer-vaccine-phase-3-trial

EXPERTS SAY: COVID-19 Vaccines Have Serious Safety Concerns

Michael Yeadon, Ph.D., a former vice-president and chief scientific adviser of Pfizer, and Wolfgang Wodarg, MD, lung specialist, filed an application with the European Medicine Agency (EMA) for the immediate suspension of all SARS CoV 2 vaccine studies, citing many potential safety concerns that were not studied in animal models before being rushed to humans, including the potential to cause female infertility. They too cite inadequate trial designs that use PCR tests to diagnose cases.

“If ADE occurs in an individual, their response to the virus can be worse than their response if they had never developed an antibody in the first place. This can cause a hyperinflammatory response, a cytokine storm, and a generally dysregulation of the immune system that allows the virus to cause more damage to our lungs and other organs of our body. . . ADE has proven to be a serious challenge with coronavirus vaccines, and this is the primary reason many of such vaccines have failed in early in-vitro or animal trials.

READ THE FULL DOCUMENT HERE: “https://informedchoicewa.org/wp-content/uploads/2020/12/Wodarg_Yeadon_EMA_Petition_Pfizer_Trial_FINAL_01DEC2020_EN_unsigned_with_Exhibits.pdf

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