| The United States’ health bureaucrats initiated Operation Warp Speed to fast track a COVID-19 so-called “vaccine.” On December 11, the FDA approved the Pfizer and BioNTech COVID “vaccine.” This “vaccine” was approved without any animal studies and without any long term human studies. This means that the individuals who take the “vaccine” will be the guinea pigs. The COVID-19 “vaccine” is manufactured using cells derived from aborted human babies in the 1970s. More accurately this so-called “vaccine” is an experimental gene therapy. The theory behind conventional vaccines is to inject a small amount of the infecting virus’ protein into your body, which in turn would cause your immune system to produce antibodies to that virus. The COVID-19 “vaccine” works differently. The COVID-19 experimental gene therapy will be the first of its kind, a messenger ribonucleic acid (mRNA) treatment. The theory behind thIs mRNA injection is that when it is injected into your body, the mRNA will insert itself into your cells and begin producing the coronavirus spike protein. There is no way to know for how long your cells will produce coronavirus particles or if they will ever stop producing them. In turn, your immune system is expected to produce antibodies to the coronavirus protein made by your own cells. Your immune system will be hyper charged and will overreact when exposed to any type of coronavirus in the future. This is what happened in past animal studies using mRNA experimental gene therapy against other types of coronaviruses in animals in 2005 and 2012. Because the animals died from an immune system hyper reaction, the “vaccine” was not used in humans. This is the first time an mRNA “vaccine” has ever been used in humans. It carries risks, including systemic inflammatory hyper reactions and the development of autoimmune conditions. Historically, all vaccines have undergone animal safety testing. The COVID-19 “vaccine” is the first ever not to be scheduled to undergo any animal safety testing. So humans are literally going to be the guinea pigs. Routinely, before a vaccine is approved by the FDA, it undergoes not only animal testing, but also two years of testing on humans to determine if there are any long-term adverse effects. The COVID-19 “vaccine” has only been tested on humans for a couple of months. Wouldn’t it be prudent to have long term human studies on this vaccine before recommending mass immunization? Adverse effects are inevitable. Already in the United States, there have been over 40,000 individuals who have reported adverse effects and several hundred deaths reported in those who took this experimental therapy in the first month of its use. Routinely, only 10 percent of the adverse effects are reported, which means there could be upwards of 400,000 individuals who have experienced adverse effects. In virtually all vaccines and drugs, post-approval adverse side effects occur, and sometimes they are serious enough to result in withdrawal from the market. You may not be aware that pharmaceutical companies are protected from lawsuits for any injury caused by vaccines. In 1986, Congress passed the National Childhood Vaccine Injury Act, which removed pharmaceutical companies’ liability for vaccine injuries. A federal Vaccine Injury Compensation Program (VICP) was created to evaluate and to compensate, with your tax dollars, individuals harmed by vaccines, basically letting pharmaceutical companies off the hook. The pharmaceutical companies that produce the COVID-19 “vaccines“ will generate enormous profits with no downside risk of product liability. With all the unknowns and uncertainties about potential adverse side effects of the COVID-19 experimental gene therapy “vaccine”, I am not recommending this treatment. It is important to strengthen your immune system through vitamin and mineral supplementation, healthy eating, natural hormone replenishment, support of the adrenal gland, treatment of allergies, exercise, a good night’s sleep, and getting down to an ideal body weight. It seems wise to take charge of your health in this manner. The COVID-19 infection poses no significant health risk, except in the infirm, elderly and those with severe pre-existing conditions. In general, people who contract COVID-19 have mild to moderate symptoms for a few days, similar to the flu, and their survival rate is 99.98%. This experimental gene therapy will not eradicate the coronavirus that causes COVID-19, any more than the flu vaccine has eliminated the flu. These viruses mutate, so the flu vaccination that is given annually is derived from the previous year’s flu virus, which was a different strain. It will be the same case with the coronavirus “vaccine.” The public health authorities state that this so-called “vaccine” will not necessarily prevent a person from contracting a coronavirus or spreading the virus. They recommend that masking and social distancing continue to be practiced. With no promise of protection from this experimental gene therapy “vaccine,” and all the potential adverse side effects, why would you risk taking it? The panic and mass hysteria created by government health bureaucrats, mainstream media, and politicians is all about control, power and money. I have already written extensively about the ineffectiveness and dangers of wearing masks, social distancing, closing of businesses, and lock downs. We need to get back to work, back to school, and back to church. Let the virus run its course so that we can develop herd immunity which is far more effective and safe than this experimental gene therapy “vaccine” could ever be. | 
