39-Year-Old Woman Dies 4 Days After Second Moderna Vaccine, Autopsy Ordered
Kassidi Kurill’s family said she had no known medical issues or pre-existing conditions, but her heart, liver and kidneys shut down after her second dose of the Moderna vaccine.
A 39-year-old woman from Ogden, Utah, died Feb. 5, four days after receiving a second dose of
Moderna’s COVID vaccine, according to
CBS affiliate KUTV.
Kassidi Kurill died of organ failure after her liver, heart and kidneys shut down. She had no known medical issues or pre-existing conditions, family members
said.
KUTV uncovered the death as part of its
investigation into
COVID vaccine side effects. The investigation involved looking into reports submitted by Utah residents to the
Vaccine Adverse Event Reporting System (VAERS).
According to
The Salt Lake Tribune, there were four deaths in Utah reported to VAERS in January and February,
including Kurill’s.
KUTV reported that doctors at
Intermountain Medical Center recommended Kurill’s family request an autopsy, and the family agreed.
The medical examiner could not say whether the autopsy would be automatically forwarded to the Centers for Disease Control and Prevention (CDC) and U.S Food and Drug Administration (FDA).
Dr. Erik Christensen, Utah’s chief medical examiner,
said proving vaccine injury as a cause of death almost never happens. “Did the vaccine cause this? I think that would be very hard to demonstrate in autopsy,” Christensen
told KUTV.
Read more:
39-Year-Old Woman Dies 4 Days After Second Moderna Vaccine, Autopsy Ordered
20+ Countries Suspend Use of AstraZeneca Vaccine, But Regulators Insist ‘Benefits Outweigh Risks’ (Because they are psychopaths and liars)
WHO and the EMA are investigating reports of blood clot-related injuries and deaths after the AstraZeneca COVID vaccine, but both say there’s no reason to stop using the vaccines.
More than 20 countries have either suspended or said they will delay Oxford-AstraZeneca vaccinations based on reports of deaths or injuries — in most cases related to blood clots — in healthy people who received the vaccine.
Prosecutors in Northern Italy announced Monday they had seized a batch of 393,600 shots of the AstraZeneca COVID vaccine following the death of a 57-year-old man hours after he was vaccinated, reported Reuters.
Meanwhile the World Health Organization (WHO) is standing firm in its support of the vaccine. In a press conference today, WHO Director General Tedros Adhanom Ghebreyesus said, “This does not necessarily mean these events [deaths and injuries] are linked to the vaccine, but it’s routine practice to investigate them, and it shows that the surveillance system works and effective controls are in place.”
According to news reports, WHO’s vaccine safety experts were meeting today to discuss the vaccine. WHO had previously said that an ongoing analysis by its vaccines advisory committee has not established a causal link between the vaccine and blood clots and countries should keep using it, reported The Telegraph.
Regulators in Europe also defended the vaccine telling news outlets that the “benefits outweigh the risks.” Still, the European Medicines Agency (EMA) is investigating reports of blood clots in vaccine recipients and will release its findings Thursday, according to Nasdaq.com.
Read More: 20+ Countries Suspend Use of AstraZeneca Vaccine
Number of Pregnant Women suffering Miscarriage after having Covid Vaccine increases by 483% in just 7 weeks
We’re saddened to report that the eighth update on adverse reactions to the Covid vaccines reported to the MHRA Yellow Card Scheme has seen yet another increase in the number of women suffering the heartbreak of losing an unborn child.
The Government have released weekly reports on adverse reactions to the experimental Covid-19 vaccines, the first of which covered data inputted to the MHRA Yellow Card Scheme from the 9th December 2020 through to the 24th January 2021. Their latest report (
find it here), which is the eighth to be released covers data inputted to the MHRA Yellow Card Scheme from the 9th December 2020 though to the 14th March 2021.
Just seven weeks separate the first and eighth report, and the shocking increase in the number of women losing their unborn and newborn child in that time due to having either the Pfizer or AstraZeneca Covid vaccine is appalling.
This was the Governments own advice upon emergency approval of the Pfizer / BioNTech vaccine
Read More: Number of Pregnant Women suffering Miscarriage after having Covid Vaccine increases by 483% in just 7 weeks
Number of ‘Covid Vaccine’ Injuries Reported to VAERS Surpasses 50,000, CDC Data Show (and it’s estimated that no more than ten percent of incidents are reported)
VAERS data released today showed 50,861 reports of adverse events following COVID vaccines, including 2,249 deaths and 7,726 serious injuries between Dec. 14, 2020 and March 26, 2021.
Data released today by the Centers for Disease Control and Prevention (CDC) on the number of injuries and deaths reported to the Vaccine Adverse Event Reporting System (VAERS) following COVID vaccines revealed steadily rising numbers, but no new trends. VAERS is the primary mechanism for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.
Every Friday, VAERS makes public all vaccine injury reports received to the system as of Friday of the previous week. Today’s data show that between Dec. 14, 2020, and March 26, a total of 50,861 total adverse events were reported to VAERS, including 2,249 deaths — an increase of 199 over the previous seven days — and 7,726 serious injuries, up 631 over the same time period.
Of the 2,249 deaths reported as of March 26, 28% occurred within 48 hours of vaccination, 19% occurred within 24 hours and 43% occurred in people who became ill within 48 hours of being vaccinated.
In the U.S., 136.7 million COVID vaccine doses had been administered as of March 26.
Read More: Number of COVID Vaccine Injuries Reported to VAERS Surpasses 50,000, CDC Data Show
EMA Contradicts Senior Official’s Claim of ‘Clear Link’ Between AstraZeneca Vaccine and Blood Clots
A senior official from the European Medicines Agency (EMA) was quoted earlier today as saying there is a “clear” link between the Oxford-AstraZeneca COVID vaccine and a rare blood clotting syndrome — but hours later the EMA denied having already established a causal connection between the vaccine and blood clots.
In a statement to Agence France-Presse, the EMA said today it had “not yet reached a conclusion and the review is currently ongoing,” adding it expected to announce its findings on Wednesday or Thursday. Marco Cavaleri, the EMA’s head of vaccines, had earlier told Italy’s Il Messaggero newspaper that in his opinion, “it is clear there is a link with the vaccine, but we still do not know what causes this reaction.”
Cavaleri said among younger vaccinated people there was a higher-than-expected number of cases of cerebral thrombosis — blood clotting in the brain — compared with the general population.
He added the EMA would issue an updated recommendation on the shot Wednesday and would officially announce a connection “in the next few hours,” but would not likely be in a position this week to give an indication regarding the age of individuals to whom the AstraZeneca shot should be given.
Read More: EMA Contradicts Senior Official’s Claim of ‘Clear Link’ Between AstraZeneca Vaccine and Blood Clots
Study: mRNA-Based Vaccines And The Risk Of Prion Disease
Vaccines have been found to cause a host of chronic, late developing adverse events. Some adverse events like type 1 diabetes may not occur until 3-4 years after a vaccine is administered [1]. In the example of type 1 diabetes the frequency of cases of adverse events may surpass the frequency of cases of severe infectious disease the vaccine was designed to prevent.
Given that type 1 diabetes is only one of many immune mediated diseases potentially caused by vaccines, chronic late occurring adverse events are a serious public health issue.
The advent of new vaccine technology creates new potential mechanisms of vaccine adverse events. For example, the first killed polio vaccine actually caused polio in recipients because the up scaled manufacturing process did not effectively kill the polio virus before it was injected into patients. RNA based vaccines offers special risks of inducing specific adverse events.
One such potential adverse event is prion based diseases caused by activation of intrinsic proteins to form prions. A wealth of knowledge has been published on a class of RNA binding proteins shown to participating in causing a number of neurological diseases including Alzheimer’s disease and ALS. TDP-43 and FUS are among the best studied of these proteins [2].
The Pfizer RNA based COVID-19 vaccine was approved by the US FDA under an emergency use authorization without long term safety data. Because of concerns about the safety of this vaccine a study was performed to determine if the vaccine could potentially induce prion based disease.
Methods
Pfizer’s RNA based vaccine against COVID-19 was evaluated for the potential to convert TDP-43 and or FUS to their prion based disease causing states. The vaccine RNA was analyzed for the presence of sequences that can activate TDP-43 and FUS. The interaction of the transcribed spike protein with its target was analyzed to determine if this action could also activate TDP-43 and FUS.
Read more:
Study: mRNA-Based Vaccines And The Risk Of Prion Disease
She was fit and healthy and had ‘everything to live for’… but died suddenly after taking ‘Covid’ fake vaccine, having suffered alone without her family to hold her hand
The family of a young mum ‘who had everything to live for’ say they are heartbroken after she died from a rare brain condition.
Rachel McKinney, 35, leaves behind her husband Kevin, stepson and two sons aged 8 and 12, after her tragic death on April 3.
The care home nurse from Stockport began developing symptoms of confusion, and slurred speech in February this year.
She had received both doses of the Pfizer vaccine in December and January and reported classic side effects, her sister Gemma said.
But a month later, her family became increasingly concerned as she displayed signs of a stroke, and Rachel was advised by 111 to attend Stepping Hill Hospital.
Due to Covid restrictions, her family were not allowed to accompany Rachel, and received a text to say she’d had an MRI scan which showed she had inflammation of the brain.
The mum-of-two was transferred to Salford Royal Hospital eight days later when a bed became available.
Her condition had quickly deteriorated, Gemma said.
“In the first few days she was mobile and able to leave the ward and go and sit in the car with her husband and sons,” she said.
“Then she lost her mobility and couldn’t leave the hospital and so she wasn’t able to see anyone.
Read more:
She was fit and healthy and had ‘everything to live for’… but died suddenly after taking ‘Covid’ fake vaccine, having suffered alone without her family to hold her hand