Dangers of COVID-19 Experimental
Gene Therapy “Vaccine”. Just Say “No!”

Steve Hotze, M.D.

The United States health bureaucrats initiated Operation Warp Speed to fast track a COVID-19 vaccine. On December 11, the FDA approved the Pfizer-BioNTech “vaccine,” and Moderna’s was approved a week later. These “vaccines” were approved without any animal studies and without any long-term human studies. This means that the individuals who get them are guinea pigs.

These “vaccines,” which are manufactured using cells derived from human babies that were aborted in the 1970s, should more accurately be called experimental gene therapy. They are an untested, unproven gene treatment that poses a much greater danger to your health than COVID-19 itself.

Unlike Any Previous Vaccine

The theory behind conventional vaccines is to inject a small amount of the infecting virus or bacteria protein into your body, which in turn will cause your immune system to produce antibodies to that infecting organism.

The new COVID-19 “vaccine” is a messenger ribonucleic acid (mRNA) experimental gene therapy, and it works much differently. The theory behind it is that when this mRNA is injected into your body, it will insert itself into your cells and begin producing coronavirus spike proteins. In turn, your immune system is expected to produce antibodies to the coronavirus protein made by your own cells.

There is no way to know how long your cells will produce these proteins, or if they will ever stop producing them! Your immune system will be hypercharged and will overreact when exposed to any type of coronavirus in the future. This is what happened when mRNA experimental gene therapy was used against other types of coronaviruses in animals in 2005 and 2012. The animals died from an immune system hyper-reaction.

Because these are the first mRNA “vaccines” ever used in humans, you would think they would have been first tested and proven safe in animal studies and have at least two years of human testing, which are routinely required. Instead, the COVID-19 mRNA “vaccine” was only tested on humans for a couple of months. Wouldn’t it be prudent to have long term-human studies before recommending mass vaccination?

40,000+ Adverse Effects in the First Month

Adverse effects are inevitable. In the first month of use, there were more than 40,000 documented adverse reactions in the U.S., including thousands of cases of anaphylactic shock and serious neurological problems. Because only 10% of adverse effects are routinely reported, hundreds of thousands have likely been harmed. That is only in the first 30 days! As of February 14, there were also 934 deaths in individuals who had received this experimental gene therapy, including baseball great, Hank Aaron.

Even more worrisome are delayed and long-term adverse effects. The mRNA “vaccine” turns on the production of COVID-19 proteins, but it has no off switch. It just keeps on replicating, and the immune system keeps on mounting an immune response. That is why some researchers are concerned that it may provoke autoimmune reactions, setting you up for a lifetime of serious inflammatory disease.

Another major concern is the possibility that the COVID-19 “vaccine” can make infections worse. There is convincing evidence that this experimental gene therapy may trigger “antibody-dependent enhancement” and increase the virus’s ability to infect your cells. In other words, if you come down with the infection after being vaccinated, you may have a much worse case than if you had never had the “vaccine.” Many experts are predicting a surge of life-threatening infections, inflammatory disorders and deaths in the coming months for those who have been vaccinated.

Of course, the blame will be placed on a mutant, particularly virulent strain of the virus, rather than on a poorly tested experimental gene therapy. Even if it were acknowledged, the U.S. government, which has spent $12.4 billion on COVID-19 vaccines so far, would foot the bill for damages incurred. By law, pharmaceutical companies cannot be sued for any injury caused by any vaccine. So, they are reaping enormous profits with no downside risk of product liability.

Not Only Dangerous but Ineffective

Not only is the media downplaying the “vaccine’s” side effects, but they also seem content to simply repeat the drug makers’ overly optimistic claims of efficacy.

You have probably heard that both the Pfizer and Moderna vaccines are 95% effective. This is a false claim. Yet, the medical establishment and the government bureaucrats have simply taken these pharmaceutical companies’ word for it and are encouraging everyone to line up for their “vaccines.”

At the time the Pfizer-BioNTech and Moderna products were approved, these pharmaceutical giants had failed to release most of the raw data from their vaccine trials. In fact, they are still withholding much of it. However, now that more of it is available for review, a different picture is emerging.

British Medical Journal (BMJ) Associate Editor Peter Doshi, who had the opportunity to review the available data, pointed out the inconsistencies and weaknesses of the pre-approval trials. He concluded that rather than the widely publicized 95% effective rate, these “vaccines” are, at best, 19% effective. At this low rate, they would never have been approved!

Health Bureaucrats Are Flying Blind

There are still many unknowns about this experimental gene therapy. There is no indication that it saves lives or prevents spreading the infection to others, which is why health bureaucrats continue to recommend masking and social distancing.

There is no data on its effectiveness and safety in frail, elderly people, who are at the greatest risk of serious disease and death.

How long will this meager protection last? Three months? A year? Is it safe and effective? What about people with compromised immune systems and the elderly? Why do people who have already had COVID-19 still need to get vaccinated?

The pre-approval trials addressed none of these important issues. Nobody has any idea, yet they are plowing ahead with plans to vaccinate the entire population.

Bottom line, this experimental gene therapy will not eradicate the coronavirus that causes COVID-19 any more than the flu vaccine has eliminated the flu. COVID-19 is here to stay. Even without a vaccine, infections will slow as more people develop natural herd immunity.

Just Say “No!”

Why in the world would you risk all the known and unknown, short and long-term side effects of a vaccine that was inadequately tested, rushed through the approval process at “warp speed,” and found to be much less effective, yet much more dangerous than initially promised? I am advising our guests here at Hotze Health & Wellness Center to just say, “No!”

COVID-19 infection poses no significant health risk except for infirm, elderly people, and those with severe pre-existing conditions. Most individuals who contract COVID-19 have mild to moderate symptoms for a few days, similar to the flu, and their survival rate is 99.98%.

Of course, it is important to strengthen your immune system with vitamin and mineral supplementation, healthy eating, natural hormone replenishment, treatment of allergies, exercise, a good night’s sleep, and maintaining your ideal body weight. Aside from that, let’s allow the virus to run its course so that we can develop herd immunity, which is far safer and more effective than this experimental gene therapy “vaccine” could ever be.

The panic and mass hysteria created by government health bureaucrats, mainstream media, and politicians are all about control, power, and money. I have written extensively about the ineffectiveness and dangers of wearing masks, social distancing, the closing of businesses, and lockdowns. We need to get back to work, back to school, and back to church.

Dr. Hotze is the founder and CEO of the Hotze Health & Wellness Center in Houston, Texas
www.hotzehwc.com

References

Selected Adverse Events Reported after COVID-19 Vaccination. CDC. Feb. 16, 2021. https://www.cdc.gov/coronavirus/2019-ncov/vaccines/safety/adverse-events.html

Cardozo T, et al. Informed consent disclosure to vaccine trial subjects of risk of COVID‐19 vaccines worsening clinical disease. 2020 Oct 28. Int J Clin Pract. e13795. https://doi.org/10.1111/ijcp.13795

Doshi P. Pfizer and Moderna’s ‘95% effective’ vaccines—we need more details and the raw data. The BMJ Opinion. Jan. 4, 2021. https://blogs.bmj.com/bmj/2021/01/04/peter-doshi-pfizer-and-modernas-95-effective-vaccines-we-need-more-details-and-the-raw-data/

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