Michigan Mom Dies 11 Days After Vaccine, CDC ‘Investigating’

Health professionals are obliged to give informed consent on all medical procedures. Among those procedures are coronavirus vaccines, but numerous Americans aren’t aware of the shots’ side effects!

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Maybe it’s unwieldy to go through the entire list of side effects at the minute-clinic vacation sites, or perhaps it confronts Biden’s massive vaccine campaign.

Would Americans risk their lives and take the shot if they knew the consequences? I don’t think so.

Johnson & Johnson are downplaying their COVID vaccines’ side effects, having a short pause in April because of the reports of blood clots.

However, the pause didn’t come at the right time for Annie VanGeest. She was a mother of four children and died only eleven days after getting the shot.

Her tragic death at the age of 35 came as a result of an acute subarachnoid hemorrhage, aka bleeding between the brain and tissue around it. The death was avoidable, with the FDA and CDC responsible.

CDC is analyzing VanGeest’s death secretly. But Twitter accounts are commenting on the safety risks of the Johnson and Johnson ‘’vaccine’’, especially on young women.

The victim’s doctor sent a report to the CDC on VAERS.

Because her death certificate reads natural causes – acute subarachnoid hemorrhage, I don’t think that CDC will seriously analyze her report.

ClickonDetroit covered this story with more details.

In a statement, her family said the 35-year-old wife and mother of four died “as the result of complications after receiving the Johnson & Johnson COVID-19 vaccine.”

But at this point, neither doctors nor the CDC have a way to know that for sure.

VanGeest’s physician filed a Vaccine Adverse Event Reporting System (VAERS) report to the CDC. The VAERS is a vaccine safety system managed by CDC and the Food and Drug Administration (FDA). VAERS accepts reports of possible side effects — also called “adverse events” — following vaccination.

The system is not designed to determine whether a reported adverse event was caused by the vaccine, but serves as an early warning system and helps CDC and FDA identify areas for further study. When VAERS receives reports of serious illness or death after vaccination, VAERS staff contact the hospital where the patient was treated to obtain the associated medical records to better understand the adverse event.

VanGeest’s death certificate lists subarachnoid hemorrhage as the cause of death. It is not known by Local 4 if there were any associated conditions such as a low platelet count or cerebral venous sinus thrombosis. The combination of the latter two conditions are the reason for the initial pause in the administration of the J&J vaccine. The pause was not caused by a concern over an increased rate of subarachnoid hemorrhage.

When the CDC restarted the J&J vaccine on April 23, it acknowledged there would likely be more cases of the rare blood clots but it believed doctors had a better understanding of how to treat it and it did not discourage anyone from getting it.

Officials said a type of blood clot called cerebral venous sinus thrombosis and low levels of blood platelets were seen in these cases.

All six cases occurred in women between the ages of 18 and 48, and symptoms began six to 13 days after vaccination, according to authorities.

Usually, an anticoagulant drug called heparin is used to treat blood clots, but in these instances, alternate treatments are used because administration of heparin could be dangerous, officials said.

This occurrence is extremely rare — it was identified in just six people out of the 6.8 million who had received the Johnson & Johnson vaccine.

Do you think that we will remain silent because the mass media say that VanGeest’s death was a coincidence and not caused by the vaccine? Well no! We don’t believe that the young mother’s death was a coincidence. We believe that the coronavirus shot caused it!

Target 8 asked for answers from Johnson & Johnson, but VanGeest wasn’t mentioned in their response!

There is no greater priority than the safety and well-being of the people we serve, and we carefully review reports of adverse events in individuals receiving our medicines or vaccines. Any report about an individual receiving our COVID-19 vaccine and our assessment of that report is shared with the U.S. Food and Drug Administration and other appropriate health authorities. This is part of the established process to inform health authorities’ comprehensive surveillance programs that monitor the overall safety of medicines, as well the vaccines authorized for use against this pandemic.

J&J, together with the mainstream media, are silent about the tragic loss!

Each and every vaccine, especially the coronavirus vaccines, aka experimental drugs, must come with informed consent!

Every life matters, even those lost to vaccines!

We advise you to read the side effect first, then decide if you will get the vaccine!

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