On the same day he praised the vaccines, Ken Buck went on Fox Business and said he would NOT take the vaccines after all. He said he is “more concerned about the safety of the vaccine” than the “side effects of the disease.”
“It is my choice. I’m an American and I have the freedom to decide if I’m going to take a vaccine or not and, in this case, I’m not going to take the vaccine,” Buck said. “I think it is one of those issues that Americans have to make that decision for themselves and I hope that we don’t get to the point where either corporations or the government are requiring this vaccine. I think that is a terrible mistake in this country,” he added.
In the first week after Pfizer’s vaccine was released, the FDA recorded 3,150 health impact events that upended people's daily activities. These people were unable to perform normal daily activities, were unable to work, and required care from a doctor or health care professional. Out of 112,807 vaccine recipients, a stunning 2.79 percent people fell victim to the vaccine injuries, which occurred in the first four days after the experiment was unleashed. This rate of injury should warrant a national emergency; the vaccine experiment should be halted at once. If preventing peak hospital capacity is important (like it was during the national shutdown of 2020), then why would public health authorities allow thousands of cases of hospitalization, medical emergency, and debilitating injury to be deliberately caused? The problems with this experimental vaccine protocol have only just begun. (Related: Moderna coronavirus vaccine causes side effects in over 50 percent of patients; antibodies disappear in 2-3 months, rendering the vaccine pointless.)
In order to approve experimental mRNA inoculation in record time, the FDA had to grant emergency authorization to the vaccine makers. In order to get emergency authorization, Pfizer and Moderna had to aggressively prove that there are no therapeutics available. This is why there was a tremendous effort to suppress all therapeutics, especially hydroxychloroquine and zinc, which were used to save lives. This life-damning agenda to cash in on vaccines is also the reason why public health officials made no mention of vitamin D, vitamin C and a host of nutraceuticals that can prevent and shorten the duration of illness, lessen viral load and speed up recovery. In essence, the FDA and the pharmaceutical industry colluded to sow disinformation about effective therapeutics and prophylactics while lying about the nutrition, treatments and the increasing survival rate that guarantees real immunity.
The investment in vaccine science was so astronomical, the project was ultimately too-big-to-fail. It had to be forced into existence by politicians, lest the stock market crash. The vaccines are now being pushed onto people who have immune-deficiencies and underlying conditions. These are the people who are more prone to vaccine injury and allergic reactions caused by polyethylene glycol and other foreign ingredients in the vaccines. These are also the people who will be susceptible to pathogenic priming, where their vaccinated immune system is primed to overreact once its is exposed to subsequent infection later on. Pathogenic priming is a serious issue that will cause even more hospitalizations, especially in older adults. All previous attempts to create coronavirus vaccines caused animals to die upon subsequent infection with the real virus.
Representative Buck is smart enough not to take the vaccine, but he erroneously insists that at-risk populations should subject themselves to it. “I think what we should do is we should focus on the at-risk populations in America, make sure those are the people that get this vaccine first. Make sure that the health care workers who want the vaccine get the vaccine as soon as possible.”
Despite Buck’s good intentions, his sloppy advice on vaccination validates his most important argument: Government officials should NOT be practicing medicine or mandating anything on the population!