by 2nd Smartest Guy in the World, 2nd Smartest Guy in the World:
This article was inspired by a Subscriber’s recent comment in the article entitled, REPOST: Ivermectin May Defeat Cancer and Other Common Chronic Diseases of Aging, where he shared his positive and most surprising “side effect:”
As per my above reply, we know that Ivermectin may in fact attenuate arthritis, and even fully cure it. The conclusion of the first cited study Evaluation of therapeutic potential of ivermectin against complete Freund’s adjuvant-induced arthritis in rats: Involvement of inflammatory mediators:
TRUTH LIVES on at https://sgtreport.tv/
Ivermectin has significant antiarthritic properties and can be a novel treatment agent for the management of rheumatoid arthritis patients suffering from strongyloidiasis.
In the second cited study, the most important sentence actually touches upon some of the admitted DEATHVAX™ adverse events:
Some antiparasitics have also been used to boost immunity in a number of human diseases including leprosy, Hodgkin’s disease, rheumatoid arthritis, and in adjuvanted therapy of colorectal cancer.
Given that even prior to the slow kill bioweapon rollout too many Americans were already exposed to dangerous environmental toxins, pre-Modified mRNA deleterious vaccines, processed foods, sodas, sedentary lifestyles, and so on and so forth, we know that the average person was existing in a hyper-inflammatory state. Said hyper-inflammatory conditions promote all kinds of diseases, not limited to cancer.
Introducing a genetically modifying DEATHVAX™ to the average inflamed person was a guaranteed bio-disaster, with elevated preexisting inflammation becoming a VAIDS baseline of hyper-inflammation, as the “vaccine” spike protein (SP 2) ravaged the entire body, and kicked off a plethora of diseases, including turbo cancers.
As the body that was contaminated into transforming itself into a spike protein factory commences to attack itself, the immune system rapidly degrades, and as the p53 protein responsible for cancer suppression is decimated by SP 2 all while ACE2 receptors are attacked and fibrils clump together to promote prion-based diseases (brain damage, premature early onset dementia and Alzheimer’s are also exacerbated by a hyper-inflammatory state), the “vaccinated” subject is reduced to a metabolic disaster zone.
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