We know that 80% of people who allegedly die from the virus are the ones ranging from 70-80 years of age, because they have other co-morbidities and a very poor immune system. Now they want to vaccinate children from 3 years of age, whose immune systems are not yet formed. This has serious consequences which could alter their immune system and develop auto-immune diseases or even modify the children’s genome. In reality, the vaccine is gene therapy and may be dangerous even for adults.
According to Dolores Cahill, Ph.D., geneticist, and immunologist from the University of Dublin (Ireland), the RNA vaccine is dangerous since after a few months the antibodies of our organism can start to attack our organs that manufacture the viral protein spike because of the RNA gene therapy vaccine. She explains the effects of the vaccine will manifest a few months after vaccination. Because of the competitive speed between laboratories to produce these vaccines decision makers didn’t take into consideration the alerts from various geneticists that warned the health authorities about this danger. Also, they were quick to eventually remove from the market any natural compounds with claims that they are toxic or even forbidden. For example, the use of the plant artemisinin both in tea or tablets that has shown efficacy against covid-19, because the WHO claims they have not yet any idea of its innocuousness. Can you believe this?!
I believe this thinking is insane and dangerous. If we are looking at Autism in the US in 1985, 1 child out of 2500 developed autism. Then in 1995, 1 out of 500, then in 2014, 1 out of 50. It is expected for 2025 that half of the children born in the US will develop autism, while vaccination is pointed out solely as a serious possible risk. So what comes next after this vaccination for children!?
As we age our immune system function tends to decline due to a process called immunosenescence.
Figure 4: Hypothesized double-sided mechanism of Sars-Cov-2 and NK Cell Interaction. In case of effective immune system response, NK cells express the activation marker CD107a and release IFNy, IL-2, and TNFα (right side). In case of exhaustion, NK cells overexpress the inhibitory NKG2A receptor, which suppresses T-cell and NK cytotoxic function favoring a pro-inflammatory condition (left side).