Baby El
November 13, 2021 6:21 pm
we had a company town hall meeting on Friday.
A question was asked if our long and short term disability covered adverse effects from the mandated notavax.
They had no idea.
Someone else asked how many people had been out with long term or severe illness from the coof.
They don’t keep track of that… And They’re Self-Insured!!
They just want to be ignorant.
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(We need to be asking uncomfortable questions of our employers in large forums.)
Doppler
November 13, 2021 6:15 pm
The immunity from liability and discovery in litigation for vaccine manufacturers did not originate with Covid. It began in the 1980s when vaccine manufacturers complained to Congress that such litigation, and the embarrassments revealed through discovery, made them want to quit making vaccines. So Congress obliged them, and created a no-fault system that allowed anyone injured to petition the Vaccine Injury Compensation Program, run by the Federal Court of Claims, for compensation, out of Congressional appropriations.
While the flu vaccine causes GBS in a substantial number of cases, the theory goes, so does the flu, and more cases are avoided than caused by vaccines.
https://www.hrsa.gov/vaccine-compensation/index.html
The drug companies are immune from claims and discovery, provided that they reveal to the FDA, which puts on the package insert, all the adverse effects known to occur from a particular vaccine. So read the insert. They’ve anticipated people will be injured, killed even, and they’ve persuaded Congress to take care of compensating the victims so that they won’t be deterred from making them. The VICP was supposed to deliver annual reports to Congress, but has failed to do so.
So, start with demanding thorough reports from the VICP. Or better yet, elect different Congresspersons who do not take money from Pharma.
The recent reports of “bad lots” for Pfizer-BioNTech’s Covid vaccine, to the effect that VAERS data show that about 5% of the lots produced are linked to the large majority of deaths reported to VAERS, suggests to me a different tactic:
How about getting interested organizations – Judicial Watch, ChildHealthDefense, etc., Mothers against killing our children – to sue the CDC, Pfizer-BioNTech, the Office of the Presidency, the FDA, the NIAID, seeking a TRO and Preliminary Injunction from selling and administering and mandating any new doses (especially to children) until the “bad lots” have been thoroughly investigated to determine what was it about those lots that was “adulterated,” i.e., caused so many deaths. Was it the people, the facilities, the ingredients, the procedures followed?
As soon as a cause or causes for the bad lots have been identified, and eliminated, then resumption might continue, unless the investigation turns up deliberate bad actors high enough in the organizations sued to reveal that the whole program is allowing ongoing involuntary clinical research into how to kill people with vaccines.