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"I lost my baby boy." A father's warning after teen son dies suddenly after the COVID Vaccine.

He did everything the doctors asked. When the FDA said the vaccine was safe for teens, Ernest Ramirez let his son get the vaccine. 5 days later his healthy teenage son died from an enlarged heart.

In May 2022 I was driving across the country meeting people like Riley Jones whose stories needed to be told. As I embarked across Texas, I was put in touch with Ernest Ramirez and told I needed to interview him.

I drove down to meet with Ernest in Corpus Christi, Texas. We spoke on the phone and I told him I didn’t know for sure where we would conduct the interview. Since half this battle is spiritual, I took a deep breath and told Ernest “I’m sure it will work out.”

When I got to the hotel the night before our scheduled interview, I was informed by the front desk manager ‘Angel’, that the hotel was out of the regular room I had booked and I would be upgraded to a suite. She even gave me an unusually late check-out.

Needless to say, the suite was perfect and had a couch with good lighting. Our interview was not going to have any logistical problems.

Junior’s story was expected by the FDA

Junior died from an enlarged heart. In August 2021 just 3 months after Junior died from an enlarged heart, the FDA proudly proclaimed ‘FDA Approves First COVID-19 Vaccine’.

Read FDA's Press Release

Fox News also touted the news to the world with all the other networks. The problem?

I was so surprised to see this image on August 23, 2021. Just a day before Acting Commissioner Janet Woodcock had been passed over to lead the FDA. Seemed a strange time to approve something so significant.
Wall Street Journal Headline from August 22, 2021

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The Devil’s in the Details

What Fox News and all the other news organizations failed to acknowledge was that the FDA knew there was a risk of enlarged heart, especially in boys Junior’s age. This information was not provided to most of the public and the FDA under Janet Woodcock put that little detail towards the end of their press release.

From the FDA’s Press Release on the Pfizer COVID Vaccine

Let’s see some more of that fine print. Anything in BOLD was enhanced by me for clarity.

Based on results from the clinical trial, the vaccine was 91% effective in preventing COVID-19 disease. 

More than half of the clinical trial participants were followed for safety outcomes for at least four months after the second dose. Overall, approximately 12,000 recipients have been followed for at least 6 months.

The most commonly reported side effects by those clinical trial participants who received Comirnaty were pain, redness and swelling at the injection site, fatigue, headache, muscle or joint pain, chills, and fever. The vaccine is effective in preventing COVID-19 and potentially serious outcomes including hospitalization and death.

Additionally, the FDA conducted a rigorous evaluation of the post-authorization safety surveillance data pertaining to myocarditis and pericarditis following administration of the Pfizer-BioNTech COVID-19 Vaccine and has determined that the data demonstrate increased risks, particularly within the seven days following the second dose. The observed risk is higher among males under 40 years of age compared to females and older males. The observed risk is highest in males 12 through 17 years of age. Available data from short-term follow-up suggest that most individuals have had resolution of symptoms. However, some individuals required intensive care support. Information is not yet available about potential long-term health outcomes. The Comirnaty Prescribing Information includes a warning about these risks.

Ongoing Safety Monitoring

The FDA and Centers for Disease Control and Prevention have monitoring systems in place to ensure that any safety concerns continue to be identified and evaluated in a timely manner. In addition, the FDA is requiring the company to conduct postmarketing studies to further assess the risks of myocarditis and pericarditis following vaccination with Comirnaty. These studies will include an evaluation of long-term outcomes among individuals who develop myocarditis following vaccination with Comirnaty. In addition, although not FDA requirements, the company has committed to additional post-marketing safety studies, including conducting a pregnancy registry study to evaluate pregnancy and infant outcomes after receipt of Comirnaty during pregnancy.

Ernest was never contacted by Pfizer or the FDA about his son’s enlarged heart after getting the Pfizer vaccine.

Now, while the FDA was preparing this misinformation-peddling press release, do you know what else it was doing?

It was tweeting about Ivermectin as a horse medication. Just two days before the press release and one day before Woodcock was passed over as head of the FDA.

This tweet was later forced by the courts to be taken down. If the FDA had not taken it down and settled the case, Dr. Mary Talley Bowden’s lawsuit against the FDA would have gone into the discovery phase. Based on the actions of the FDA, I wonder what Dr. Bowden would have found.

The FDA sure had a hell of a week. It was a week that kicked off a non-stop onslaught of pressure campaigns on the general population to get vaccinated. There was also a flurry of activity on Facebook forums like Shots Heard (aka #Shotsgate), resulting in medical license complaints against doctors who questioned the FDA’s narrative all across the United States.

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One other thing. The FDA wasn’t the only agency concealing risks. In May of 2021, the CDC withheld an “alert on myocarditis and mRNA vaccines”.

The CDC was aware in May of 2021 that there were myocarditis issues with the vaccines.

According to emails covered in an article by the Brownstone Institute covering revelations from DailyClout and Epoch Times:

Over the following two years, Dr. Daskalakis and his colleagues pushed the shots on every age group and deliberately withheld publishing its alert on myocarditis. Instead, the CDC sent repeated alerts encouraging Covid-19 vaccination for everyone. 

The article ends with:

They knew of the risks, and they withheld the information from the American people. Stripped of informed consent, millions of citizens took the shots while doctors like Demetre Daskalakis denied them the right to know the risks of the product.

By the way, you remember Demetre right? He’s the demonic tattooed monkey pox czar we obtained a secret recording of at the AMA joking about how to manipulate the population.

Epoch Times has an excellent timeline of all events that the CDC and FDA concealed here.

When did denial of informed consent become acceptable?

You can still help Ernest

Ernest’s trailer covered with pics and names of those killed by the FDA’s actions

Ernesto continues to fight. If you would like to donate to his efforts, visit his Give Send Go page here.

Donate to Ernesto’s Efforts to bring awareness to his Junior’s story.

You can see a more recent interview with Ernest and Dr. John Witcher, here.

Ernest's testimony to Sen. Ron Johnson

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