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Source - The SPARS Pandemic 2025-2028
Learn something today to be programed... I mean prepared for tomorrow!
The SPARS Outbreak Begins
CHAPTER ONE
In mid-October 2025, three deaths were reported among members of the First Baptist Church of St. Paul, Minnesota.
Two of the church members had recently returned from a missionary trip to the Philippines, where they provided relief to victims of regional floods. (...)
Users Beware (would you ask for it or #WeDoNotConsent)
CHAPTER FOUR
Following limited evidence of success in treating SPARS patients with Kalocivir,
the FDA issued an Emergency Use Authorization (EUA) for this drug as a SPARS therapeutic in the United States.
While Kalocivir had a positive impact against SPARS, preliminary data indicated it also caused intense
stomach cramping in a statistically significant number of adult cases. Additionally, while initial hopes
had been that Kalocivir would, in addition to treating the disease, prevent or reduce transmission, this
was not the case. Nevertheless, due to high public demand for access to viable SPARS treatments,
public health and healthcare agencies drew from existing SNS inventories of Kalocivir (several million
doses) until further production of the drug could begin. (...)
After Kalocivir was in public use for three months,
the FDA was able to release updated information about the drug’s effectiveness and the incidence of side effects.
This information came too late, however, for large portions of the general public.
In Wisconsin, where many individuals were treated
with Kalocivir, local citizens posted, Tweeted, chatted, and Zapped real-time impressions of the drug.
While some claimed the drug was effective and even life-saving, most reported no effect and claimed
that the drug had caused additional side effects, such as headaches, nausea, and body aches. (...)
VACCINE INJURY
CHAPTER SEVENTEEN
In contrast to Alyssa Karpowitz’s story, not all changes in opinion were in favor of public health
messaging. As time ped and more people across the United States were vaccinated, claims of
adverse side effects began to emerge. Several parents claimed that their children were experiencing
neurological symptoms similar to those seen among livestock exposed to the GMI vaccine. By May
2027, parental anxiety around this claim had intensified to the point of lawsuits. That month, a group
of parents whose children developed mental retardation as a result of encephalitis in the wake of
Corovax vaccination sued the federal government, demanding removal of the liability shield protecting
the pharmaceutical companies responsible for developing and manufacturing Corovax. (...)
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