Typical US problem? ... over here our statistics indicate that 60% of the current IC unit capacity (90% of pre-2020) is now occupied by covid-19 patients... (sorry for getting more off-topic)real problem is that all the statistics and data we have on COVID are politically driven
According to CDC there were 22,000 deaths in the US attributed to the flu in 2019, whereas there were over 500,000 in the deaths due to COVID in the first 12 months of the pandemic.
The common flu was never bad enough in the recent past where hospitals ran out of room in South Texas and North Dakota and patients literally died in hallways waiting for care, or where city parks in New York City were requisitioned as temporary burial grounds with morgues not being able to keep up with over 1000 excess deaths per day during the first wave.
The people who SHOULD be taking precautions are those in the higher-risk categories: the overweight, the 70+ crowd, those with high blood pressure, serious heart conditions, and perhaps diabetes.
So another logical way to look at it is this: THEY have the obligation to remain isolated or to wear double-masks, keep "social distance", etc. The other 90%? Not so much.
The problem is that only priests can anoint, confess, and, for about 90% of things,
The real problem is that all the statistics and data we have on COVID are politically driven
in protecting natural life, we endanger supernatural life by cutting off access to the sacraments.
Seconding Chris; if you put it this way, you'll probably never get an answer.Still waiting for someone to reference the Catholic moral teaching that requires Catholics to be guinea pigs taking experimental "vaccines"
“It is evident, in the light of practical reason, that the vaccination is not, as a rule, a moral obligation and must therefore be voluntary,” adding only that if the common good so indicates then “it is good to permit recommendation of vaccination, in particular to protect those who are weakest and more exposed.”
During the COVID-19 pandemic, EMA's {European Medicines Agency} conditional marketing authorisation is being used to expedite the approval of safe and effective COVID-19 treatments and vaccines in the EU.
This is in line with EU legislation which foresees that conditional marketing authorisation is used as the fast-track authorisation during public health emergencies to speed up approval and save lives.
It allows regulators to grant a marketing authorisation as soon as sufficient data becomes available to demonstrate that the medicine's benefits outweigh its risks, with robust safeguards and controls in place post-authorisation.
In a public health emergency, it can also be combined with a rolling review of data during the development of a promising medicine, to further expedite the evaluation.
robust safeguards and controls in place post-authorisation.
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