Listen to a CG Podcast with Prof. Ted Steel, Elizabeth Hart and Dr. Judy Wilyman discussing the COVID so-called “vaccines”.
Put simply, conventional vaccines use disabled or dead microbes or pharmacologically inert parts of microbes to elicit an immune response. They are not necessarily “safe”. They must be tested to determine if they are effective and safe and this usually takes about 10 years. There are many examples of unsafe vaccines which were tested for many years, released and subsequently found to be unsafe. Some vaccines have been withdrawn after fewer than 50 vaccine-caused deaths. The COVID “vaccines” have been associated with millions of deaths worldwide.
The problem is basically that it is the Spike Protein which is the toxic component of the SARS-CoV-2 virus. It is the Spike Protein that causes the pathology underlying the disease. So, why would you design a vaccine to produce in healthy people the toxic Spike Protein?
It gets worse…….The Spike Protein produced by the SARS-CoV-2 is not identical to the Spike Protein on the surface of SARS-CoV-2. The Spike Protein produced by the COVID so-called “vaccines” is designed to resist metabolic destruction and so it lasts for a long time in the blood - sometimes months (think “Long COVID”). But the lunacy does not stop there. the mRNA or DNA in the COVID so-called “vaccines” is designed to enhance the production of modified “vaccine” Spike Protein. It is the perfect storm. The results in heaps of toxic modified “vaccine” Spike Protein in the blood…..and people wonder why the excess deaths around the world has skyrocketed!
But wait…there is more. In a natural SARS-CoV-2 infection, the amount of virus (and Spike Protein on the virus) slowly ramps up over many days. But following vaccination an enormous quantity of modified “vaccine” Spike Protein is produced in some people in a short time. This is probably why there are many reported deaths within 48 hours of vaccination.
My old mate Ted Steele with an E.
https://independent.academia.edu/EdwardJSteele/CurriculumVitae
https://www.researchgate.net/profile/Edward-Steele-5
As they say in late-night infomercials: But wait; there's more! Since the first SARS outbreak c. 2002, there have been concerted efforts to develop a safe and effective vaccine against coronaviruses. Such a vaccine wouldn't just have importance in human medicine, but in veterinary medicine as well. Feline infectious peritonitis (FIP) is a frequently fatal disease in cats that is caused by a coronavirus; and bovine coronaviruses are one of the class of organisms involved in bovine respiratory disease (BRD) complex which can result in pneumonia and other problems in cattle.
Since 2002, and with renewed efforts after the MERS outbreak c. 2012, all efforts to develop a safe and effective vaccine against coronaviruses have failed at the animal-testing stage. That includes all vaccine types - whole virus, whether killed or attenuated/modified-live; subunit (e.g., specific viral proteins); and viral-vector or chimaera vaccines. The Oxford-AstraZeneca vaccine, which uses a chimpanzee adenovirus as the vector, is an example of the latter type of vaccine, but it didn't exist until 2020 or so. Likewise, the mRNA-based COVID vaccines are not included in that list because they didn't exist until the COVID-19 scamdemic.
The point is that ALL efforts to develop a coronavirus vaccine have failed because of antibody-dependent enhancement of disease in the vaccinated animals when they were subsequently challenged with the target virus (to see whether the vaccine is effective in preventing illness).
So, why on earth did Pfizer, Moderna, AZ, J&J, etc. think that they could crack this nut in under a year?! Arrogance. Ignorance. Greed.