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Guidance Regarding Mandatory Vaccination Requirements for Employees and Residents of Long-Term Care | Spilman Thomas & Battle, PLLC

To embed, copy and paste the code into your website or blog: Long-term care facilities have been the epicenter of COVID-19 infections and deaths. According to the Centers for Disease Control and Prevention (“CDC”), nursing homes and other long-term care populations are at a high risk of being affected by COVID-19 due to their congregate nature and high risk population. The CDC reports that as of December 20, 2020, there were 471,953 nationwide cases of COVID-19 cases among long-term care residents, which resulted in 92,373 deaths from COVID-19. The total confirmed COVID-19 cases for long-term care facility employees during the same period of time was 402,956 nationwide, which resulted in 1,268 deaths from COVID-19. Hopefully, with the development and distribution of COVID-19 vaccines, there will be a significant decline in cases and deaths from COVID-19 in long-term care facilities.  

A vaccination tax is needed for equity and public confidence - On Line Opinion

Vaccination is not without risk. The Prime Minister, Scott Morrison, has declared indemnification for vaccine manufacturers for adverse vaccine outcomes. What is missing is compensation for vax-injured individuals. The USA has had a vaccine injury compensation scheme (VICS) for the past three decades. The US National Vaccine Injury Compensation Program (VICP) has paid out US$4.4 billion (A$5.7 billion) for 7,575 vax injuries (from 1989 through 2020). The average settled claim was US$585,000 (A$760,000). There were 1.4 compensated injuries per million distributed vaccine doses. Of the total vax injury claims filed in the USA (n= 22,372), 94% were claims for non-fatal injury (n=21,035) and 6% were claims for death (n=1,337). Of the total claims filed, 34% were successful (n=7611), 52% were dismissed (n=11,671), and 14% did not progress to adjudication (n=3,090).

DC Passes Bill to Vaccinate Children Without Parental Consent or Knowledge

The bill that permits a child aged 11 years or older “to consent to receive a vaccine where the vaccination is recommended by the United States Advisory Committee on Immunization Practices. It also establishes that if a minor is able to comprehend the need for, the nature of, and any significant risks inherent in the medical care then informed consent is established.” The bill not only permits children of this age to provide consent to doctors and other vaccine administrators without a parent’s knowledge or consent, but also requires school administrators, insurance companies, and medical personnel to conceal a child s vaccination from their parents.

WARNING: Covid Vaccines! | Dissident Voice

by Peter Koenig / December 24th, 2020 Did you know that the US Government since 1988 paid as of 1 December 2020 more than 4.4 billion dollars to vaccine-injury victims? It’s your money, Taxpayers money. This is Health Services and Service Administration Vaccine Injury Compensation Data  The National Childhood Vaccine Injury Act ( NCVIA) of 1986 (42 U.S.C. §§ 300aa-1 to 300aa-34) which was signed into law by US President Ronald Reagan as part of a larger health bill on November 14, 1986. Under NCVIA nobody can sue a vaccine producing pharma-company or laboratory for injuries and/or death caused by a vaccine. NCVIA’s purpose was to eliminate the potential financial liability of vaccine manufacturers due to vaccine injury and death. The official explanation for the NCVIA is

Forced Vaccination in Israel - Is It Right?

Olivier Fitoussi/Flash90 To many the arrival of the new COVID-19 vaccine signals the light at the end of a dark tunnel. For others, the vaccine, or rather the regulations concerning it are a threat to civil liberties. Will Israel rule the vaccine mandatory? And how will that affect society if it does?   Cause for concern? The pandemic started not too long ago, and we already have an authorized vaccine in our hands. According to Wellcome Trust, a research-charity based in London, a vaccine normally takes about 10 years to develop, with the 1st research stage taking between 2-5 years, pre-clinical development of 2 years, a 3-phase clinical development that takes about 5 years, regulatory review of 1-2 years, and finally manufacturing and delivery.

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