HomeMy WebLinkAbout04262021_Huenke_Covid DeathFrom:Annette Huenke
To:Board of Health; Tom Locke; jmichaels@jeffersonhealthcare.org
Subject:copy of BOCC public comment with addendum
Date:Monday, April 26, 2021 9:54:21 AM
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Good morning, everyone.
The following is my public comment to the commissioners on April 26, 2021. Regarding the
death of the man reported to be the third covid death in Jefferson County, if the man received any of the three unapproved products referred to as "vaccines," no matter when, it is required
that his death be reported to VAERS, per the FDA’s Emergency Use Authorization (EUA). [My addendum follows comment, emphasis is mine, pertains to all products, not just Pfizer.]
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Commissioners:
The April 21st Leader was full of official disinformation. On the news of the passing of a man already critically ill, we’re told “COVID was, we believe, the cause of death. Had it not been
for the COVID infection, that person would have likely survived,’ Locke said.” We’re not told if he was recently vaccinated.
Purely speculative pronouncements such as “we believe” and “would have likely survived”
are apparently reserved for public officials only. If one used similar conjecture about someone dying minutes, hours or days after the covid shot, they'd be maligned as being anti-science,
then censored from public discourse. The medical milieu is rife with this sort of double standard.
Dr. Locke goes on, crediting today’s death rate being lower than a year ago “mainly due to the
vaccination of older people and others at high risk.” More deceptive speculation, completely lacking in proof. He neglected to mention the alarming number of care homes which managed
to be covid-free until the end of 2020, when the ‘vaccine’ program came along, bringing with it shocking numbers of post-injection deaths and soaring new ‘case’ counts.
Locke refers to those who have taken the jabs as “fully immunized,” suggesting the shots
provide immunity, an outcome Locke has claimed in the past. None of the trials were designed to prove that, nor that they prevent transmission or serious disease, or save lives. The trial
endpoint was reduction of symptoms. Expect a cascade of obfuscation around vaccine failure, which has recently been euphemistically rebranded as ‘vaccine breakthrough.’
Most troubling of all was the article's boasting about the coming “vaccination clinic for 16 and
17 year olds — called “Teen Spirit”… to give the Pfizer medicine to teens.” It is perverse, malevolent distortion to refer to these products as ‘medicine.’ They are a novel, experimental
technology that has not even concluded animal studies. They are not yet approved or licensed by the FDA. Long term effects cannot be known. Their promotion to teens as a way to 'do
their part' is reckless in the extreme. If infertility or other harms result from these jabs, those of you who gleefully pushed them on this subset — not even at risk of the virus — will be
held to account. This is medical experimentation without informed consent.
Annette Huenke Port Townsend
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ADDENDUM
4. The vaccination provider is responsible for mandatory reporting of the following to the Vaccine Adverse Event Reporting System (VAERS):
• vaccine administration errors whether or not associated with an adverse event, • serious adverse events* (irrespective of attribution to vaccination), • cases of Multisystem Inflammatory Syndrome (MIS) in adults and children, and • cases of COVID-19 that result in hospitalization or death.
Complete and submit reports to VAERS online at https://vaers.hhs.gov/reportevent.html. For further assistance with reporting to
VAERS call 1-800-822-7967. The reports should include the words “Pfizer-
BioNTech COVID-19 Vaccine EUA” in the description section of the report.
5. The vaccination provider is responsible for responding to FDA requests for information about vaccine administration errors, adverse events, cases of MIS in
adults and children, and cases of COVID-19 that result in hospitalization or death
following administration of Pfizer-BioNTech COVID-19 Vaccine to recipients.
* Serious adverse events are defined as:
• Death;
• A life-threatening adverse event; • Inpatient hospitalization or prolongation of existing hospitalization; • A persistent or significant incapacity or substantial disruption of the ability to
conduct normal life functions;
• A congenital anomaly/birth defect;
• An important medical event that based on appropriate medical judgement may jeopardize the individual and may require medical or surgical intervention to
prevent one of the outcomes listed above.
[http://labeling.pfizer.com/ShowLabeling.aspx?id=14471&format=pdf]