SALT LAKE CITY, Utah – In Ogden, Utah, a woman died four days after her second dose of Modner COVID-19 vaccine. Consequently, her loved ones are waiting for the result of an autopsy.
They held a life celebration for her this past weekend. According to people around her, Kassidi Kurill was generally healthy. She was known for having “more energy” than just anyone else who was consistent around her.
She had no existing conditions. Her first shot went off without any problems from the usual pain in her arm. As a surgical technician for some local surgeons, it was necessary to be vaccinated through her work.
Where many had problems or questions and delayed inoculating, Kassidi no doubt did so. She was the first in the family to do so.
What started as arm pain and flu-like symptoms increased. Everyone at work had the symptoms, so no one in her family thought much about it.
After lying in bed for two days, she knew on the third day that something was wrong. Thursday, Feb. 4, she’s off to the local ER at about 7 p.m. She immediately started vomiting. After blood tests, they found that her liver was not good. She was then transferred.
They tried to get her a match for a kidney transplant and get her stable in the hospital. Nothing worked. After her liver weakened, her kidney and heart followed. She passed away about 30 hours after entering the emergency room.
Kassidi’s death will not go unnoticed. Now her 9-year-old daughter has to stay with her grandparents. Her father is a member of the National Guard, and as a civil servant it often works because of work and he also had to spend time overseas.
If you like, you can donate to her daughter Emilia’s GoFundMe or through America First Credit Union:
- PO Box 9199, Ogden, UT 84409
- Routing # AFCU 324377516
- Account # 9119439
As of now, 1,637 families or caregivers have reported deaths related to the VAERS vaccine. The Centers for Disease Control is the one that manages the vaccine reporting system. The CDC says there are no deaths attributed to COVID-19 vaccines. “CDC and FDA will continue to investigate reports of adverse events, including deaths, reported to VAERS,” the CDC said on its website.