Leftists Want People to Die Willingly

Pushing the Death Poke, Despite the Science

In case you’re wondering why Leftists continue to push for vaccines despite proof the vaccines are ineffective, check out this story.

A man who wasn’t dying was granted euthanasia in Colombia.

CNN reported on Colombian Victor Escobar.

Escobar became the first person in the Andean country with a non-terminal illness to die by legally regulated euthanasia. This was confirmed by his attorney Luis Giraldo last Friday.

Escobar left this video message that Giraldo sent to the media:

“We reached the goal for patients like me, who aren’t terminal but degenerative, to win this battle, a battle that opens the doors for the other patients who come after me and who right now want a dignified death.”

Appalling, right? The idea that somebody not dying and really having no reason to die can choose to die seems barbaric. Because it is. Life is meant to be precious. But when it comes to population control, you must understand what’s really at play.

This voluntary euthanasia will soon be the norm. It will be explained as “selfless”.

Soon after, voluntary euthanasia will be called “patriotic”. People will get awards, posthumously of course. These awards will speak to the “courage” of people who opt out of life. And not because those opting out believe in something else. Quite the contrary.

Their courage is to give up all that life had to offer them. However their selfless act allows one other person to enjoy all that things that life has to offer. They will have created a slot for somebody else.

Films will be made about such heroes. These films will be the “Armageddon” of the “euthanasists”, except saving the world won’t involve stopping a meteor from smashing into earth. Saving the world will be the selfless patriotic acts of those willing to stick their finger in the socket for the good of mankind.

Until then, leftists have another way to control the population.

Vaccine or Death Poke

For those who believe there is an actual covid vaccine, consider these facts. According to the History of Vaccines, by the end of the 1800s, several vaccines for humans had been developed.

They were smallpox, rabies, plague, cholera, and typhoid vaccines. However, no regulation of vaccine production existed.”

On July 1, 1902, the U.S. Congress passed “An act to regulate the sale of viruses, serums, toxins, and analogous products,” later referred to as the Biologics Control Act (even though “biologics” appears nowhere in the law). This was the first modern federal legislation to control the quality of drugs. This act emerged in part as a response to 1901 contamination events in St. Louis and Camden involving smallpox vaccine and diphtheria antitoxin.

The Act created the Hygienic Laboratory of the U.S. Public Health Service to oversee manufacture of biological drugs. The Hygienic Laboratory eventually became the National Institutes of Health. The Act established the government’s right to control the establishments where vaccines were made.

The United States Public Service Act of 1944 mandated that the federal government issue licenses for biological products, including vaccines. After a poliovirus vaccine accident in 1954 (known as the Cutter incident), the Division of Biologics Standards was formed to oversee vaccine safety and regulation. Later, the DBS was renamed the Bureau of Biologics, and it became part of the Food and Drug Administration. It is now know as the Center for Biologics Evaluation and Research.

Social Media Christmas Sale Kevin Jackson
Social Media Christmas Sale Kevin Jackson
Social Media Christmas Sale Kevin Jackson
Social Media Christmas Sale Kevin Jackson
Social Media Christmas Sale Kevin Jackson

The process of developing vaccines is typically somewhat long and complex.

In fact, you can read the in-depth process here. I find it quite interesting that the website decided they need to update their history lesson to allow for the WuFlu death poke. As the site reads:

EDITOR’S NOTE (25 JANUARY 2022): Many anti-vaccine people and organizations are not presenting the information in this article in full context. The article below covers vaccines before the current COVID-19 pandemic. We will be updating the article shortly to include the accelerated approval process of the COVID-19 vaccines. Concerning the time it takes for a vaccine to go from conception to approval and licensing, the mRNA vaccine technology used in the vaccines dates back to the 1990s.

I’m guessing the leftists in charge don’t want people holding the covid vaccine up to traditional standards.

Stages of Vaccine Development and Testing

In the United States, vaccine development and testing follow a well-established set of steps. The first stages are exploratory in nature. Regulation and oversight increase as the candidate vaccine makes its way through the process.

The initial exploratory stage includes lab and animal studies. It can last anywhere from 2 to 4 years. Then, the vaccine moves to the pre-clinical stage where animal testing is often the center of data gathering. These studies typically involve monkeys or mice. They help nail down cellular responses and establish safe dosages.

Next, a company will apply to produce an IND (Investigational New Drug). The FDA has 30 days to approve or turn-down the application.  Once approved, a vaccine can begin clinical trials with human test subjects. If a vaccine shows promise in a small, controlled experimental group, it can move on to a larger test-phase. Slowly, the test group grows larger as a placebo is introduced. All the while, careful records of reactions are maintained and verified again and again.

None of this happens lickety split. And there are a ton of hoops and hurdles to overcome. After successful Phase III trials, a vaccine can be approved and licensed. Still, the FDA continues to monitor the vaccine- even inspecting the factories where it is produced.

In fact, that is where VAERS comes into play.

VAERS

The CDC and FDA established The Vaccine Adverse Event Reporting System in 1990. The goal of VAERS, according to the CDC, is “to detect possible signals of adverse events associated with vaccines.” (A signal in this case is evidence of a possible adverse event that emerges in the data collected.) About 30,000 events are reported each year to VAERS. Between 10% and 15% of these reports describe serious medical events that result in hospitalization, life-threatening illness, disability, or death.

VAERS is a voluntary reporting system. Anyone, such as a parent, a health care provider, or friend of the patient, who suspects an association between a vaccination and an adverse event may report that event and information about it to VAERS. The CDC then investigates the event and tries to find out whether the adverse event was in fact caused by the vaccination.

The CDC states that they monitor VAERS data to:
        • Detect new, unusual, or rare vaccine adverse events
        • Monitor increases in known adverse events
        • Identify potential patient risk factors for particular types of adverse events
        • Identify vaccine lots with increased numbers or types of reported adverse events
        • Assess the safety of newly licensed vaccines

The covid vaccine was admittedly fast-tracked. But that’s not what truly concerns me. I believe there are times when we cut through the red tape in order to solve a problem. However, the fact that we’ve done nothing to address adverse effects of the vaccine is the problem.

Is it ok for unborn babies to die as a result of this vaccine? Or for heart patients to experience unrecoverable damage? Of course not. But leftists refuse to say “Stop the Presses!” Instead, they push on, even requiring vaccines as a condition of employment or service. It’s an unacceptable practice. However, leftists clearly see the vaccine as a way to wipe out part of our population. Especially the aging population that can be seen as a drain on Social Security or Medicare. Why else would we continue to force vaccinations for a virus that kills less than 1% of the population? Inquiring minds want to know.

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