Child Injured in Covid Jab Trial Is Ignored

Maddie de Garay signed up to participate in Pfizer’s COVID-19 clinical trial for 12- to 15-year-olds in early 2021. Within 12 hours of her second dose, she suffered a severe systemic adverse reaction that left her wheelchair-bound and on a feeding tube
Maddie’s severe adverse reactions have been ignored by Pfizer, the U.S. Food and Drug Administration and the Centers for Disease Control and Prevention. She’s received no help from any of them, financial or medical, and Pfizer even went so far as to lie about her status, describing it as “functional abdominal pain” in a report to the FDA
One government official who isn’t turning a blind eye to the devastating effects of the COVID shots is Florida Surgeon General Dr. Joseph Ladapo. In a January 3, 2024, press release, Ladapo is calling for an end to the use of COVID-19 mRNA shots, citing concerns about DNA fragments in the products
According to the FDA’s guidance on DNA in vaccines, “DNA integration could theoretically impact a human’s oncogenes — the genes which can transform a healthy cell into a cancerous cell,” and “may result in chromosomal instability”
The FDA has not provided any evidence that DNA integration assessments have been conducted to address the health risks listed in its own guidance on DNA in vaccines, published in 2007. Consequently, the mRNA shots are “not appropriate for use in human beings,” Ladapo says

(Mercola)—When Stephanie de Garay allowed her three children to sign up for Pfizer’s COVID-19 clinical trial for 12- to 15-year-olds, she assumed the worst that could happen was anaphylactic shock — and in that case, they’d be treated with an EpiPen and be fine. From her daughter’s perspective, the trial was a way to keep up with a close friend who had already signed up for it.

It also didn’t hurt that the trial offered monetary compensation of $119 per visit.¹ This is what prompted all three of de Garay’s children to sign up for the COVID-19 shot trial, which changed the life of de Garay’s daughter Maddie. A healthy 12-year-old girl prior to the trial, Maddie loved to dance, play soccer and spend time with her friends.

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She suffered a severe systemic adverse reaction to her second dose of the shot and struggled through 11 ER visits and four hospital admissions in the year and a half that followed. Injuries from the shot have left her unable to walk or eat — she receives her nutrition via a feeding tube — and suffering from constant pain, vision problems, tinnitus, allergic reactions and lack of neck control.²

As though the physical trauma weren’t enough, Maddie and her family were continually dismissed by the medical professionals put in place to help, ignored by the U.S. Food and Drug Administration and denied the care needed. Instead, the family was told Maddie’s problems were psychological, and she underwent cognitive-behavioral therapy, to no avail, as one might expect.

Broken Trust

In the January 21, 2024, “Full Measure” report above, investigative journalist Sharyl Attkisson reviews Maddie’s case. Maddie received her second dose January 20, 2021. Within 12 hours, frightful symptoms set in. Electric shocks were shooting up her spine and it felt like her heart was being “ripped out.”

She suffered chest and abdominal pains. Her toes and fingers turned white and ice cold. In short order, she lost feeling in her legs and could no longer walk. She started passing out and lost her swallow reflex. Despite what happened to Maddie, Pfizer announced the children’s trial had been a success, and that their COVID shot had a “favorable safety profile.”

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According to de Garay, Pfizer and U.S. regulators refused to acknowledge that Maddie had been injured by the shot. They also failed to properly record her injuries in an apparent effort to downplay the severity of them. For example, in an April 2021 disclosure to the FDA, Pfizer described Maddie’s side effects as “functional abdominal pain,”³ even though she was wheelchair bound and couldn’t even swallow food.

Maddie has now been diagnosed with chronic inflammatory demyelinating polyneuropathy (CIDP) — a rare autoimmune disease in which the immune system attacks and destroys the myelin sheaths around nerve cells. Maddie has not received any help — financial or medical — from Pfizer, the FDA or the Centers for Disease Control and Prevention.

When asked what her daughter’s ordeal has taught her, de Garay says it has opened her eyes. She used to trust government officials, doctors and hospitals, but “What I thought they were is not what they are,” she says.

Indeed, if anything, Maddie’s story should serve as a warning to all. It shows just how callous the vaccine industry and its protectors are. You are the guinea pig, and if something goes wrong, you’re on your own. You won’t even get an apology, let alone any actual aid.

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Pfizer Classified Severe Reactions as ‘Not Related’ to Shots

The FDA and Pfizer tried to hide the COVID-19 shot clinical trial data for 75 years, but the FDA was eventually ordered by the U.S. District Court for the Northern District of Texas to release trial documents on a much faster schedule. As part of the court order, 80,000 pages of documents related to the FDA’s approval of Pfizer’s COVID-19 shots were released June 1, 2022.⁴

Among those documents were case report forms (CRFs) revealing that deaths and severe adverse events took place during Phase 3 trials, most of which were classified as “not related” to the shot.⁵

Examples include a woman in her early 50s who died from a heart attack five days after she’d received the second dose of Pfizer’s experimental COVID-19 shot. Her death was listed as “not related” to the shots. The death of a teenage girl who suffered deep vein thrombosis two months after her second dose was also deemed “not related.” As reported by independent journalist Michael Nevradakis, for Children’s Health Defense:⁶

“The many serious adverse events — and several deaths — recorded during the Phase 3 trials are also apparent in a separate, massive document exceeding 2,500 pages, cataloging such adverse events.

This document lists a wide range of adverse events suffered by trial participants classified as toxicity level 4 — the highest and most serious such level.

However, not one of the level 4 (most severe) adverse events listed in this particular document is classified as being related to the vaccination … Similarly, only a small number of toxicity level 3 adverse events were indicated as having been ‘related’ to vaccination.”

The FDA Ignored Maddie’s Case

Just as it ignored the many red flags in Pfizer’s clinical trial data, the FDA also ignored Maddie’s case, even when attorneys got involved. In August 2021, the de Garays reached out to ICAN’s legal team; ICAN’s Aaron Siri now represents them. According to Siri:⁷

“What happened to Maddie is not only the story of an injury to a child, which is heartbreaking in and of itself. But Maddie was in a clinical trial that only had 1,000 children in the age bracket of 12 to 15 years old that got the COVID-19 vaccine.

When she suffered that reaction, there should have been every medical expert at Cincinnati and at the FDA that should have descended to study what happened to Maddie, because if that could happen to one in 1,000 children, the repercussions could be really devastating, especially for an infection that doesn’t harm children anywhere near that rate.”

After ICAN’s team got Maddie’s medical records and reviewed them, they believe the causal connection to Pfizer’s COVID-19 shot is extraordinarily strong. In October 2021, they sent a letter to the FDA, including all of Maddie’s medical records and highlighting how Pfizer downplayed the condition in their disclosure, describing Pfizer’s move as “at best dishonest. To regulators, it should be criminal.”⁸

In February 2022, the FDA finally responded, incredulously by saying to file a VAERS report or send a letter to CISA, the Clinical Immunization Safety Assessment Project, which is run by Dr. Kathryn Edwards, who sits on the data safety monitoring board for Pfizer’s COVID-19 shot trials. In other words, they did nothing.⁹

Maddie’s story is ongoing and, sadly, is only one of many cases of people being seriously injured or killed by COVID-19 shots and not being taken seriously — or outright discredited — by health care providers and health officials. However, there is hope, and it comes in the form of protecting your right to informed consent and the freedom to make your own medical choices. As Siri put it:¹⁰

“The hope is that we make sure that we always have the choice to say no. As long as we can say no, that is the safeguard. That is the stopgap to all of this bad conduct. It’s not going to protect those who don’t know better to say no in certain situations, but it will protect those who do …

Freedom of speech, the ability to have individual liberties. That is what will save us … The ability to become educated, to have access to information and to make informed decisions … the ability to say no about something, or a medical procedure, that we don’t want to have on our bodies or our children’s bodies.”

Florida Surgeon General Calls for Halt to COVID Shots

One government official who isn’t turning a blind eye to the devastating effects of the COVID shots is Florida Surgeon General Dr. Joseph Ladapo. Early on in the pandemic, he published articles criticizing lockdown measures and calling for the adoption of early treatment.¹¹

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In March 2022, he recommended against COVID-19 shots for healthy children,¹² making Florida the first state to break with official CDC guidance.

In February 2023, he issued an official health alert¹³ warning that the COVID mRNA shots were associated with a “substantial increase” in reports of adverse events in Florida, and that fall, he again broke off from the official policy by urging people under 65 to avoid further boosters.¹⁴

Now, in a January 3, 2024, press release, Ladapo is calling for an end to the use of COVID-19 mRNA shots, citing concerns about DNA fragments in the products.¹⁵

In a December 6, 2023, letter sent to the FDA and CDC, Ladapo outlined findings showing the presence of lipid nanoparticle complexes and simian virus 40 (SV40) promoter/enhancer DNA in the COVID shots. As noted in the Florida Health January 3 press release:¹⁶

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“Lipid nanoparticles are an efficient vehicle for delivery of the mRNA in the COVID-19 vaccines into human cells and may therefore be an equally efficient vehicle for delivering contaminant DNA into human cells. The presence of SV40 promoter/enhancer DNA may also pose a unique and heightened risk of DNA integration into human cells.”

The presence of SV40 promoter and other DNA fragments was first reported¹⁷ by microbiologist Kevin McKernan in early April 2023. McKernan is a former researcher and team leader for the MIT Human Genome project. I wrote about these findings in “Monkey Virus DNA Found in COVID-19 Shots,” posted at the end of May 2023.

According to McKernan, “Multiple assays support DNA contamination that exceeds the European Medicines Agency (EMA) 330ng/mg requirement and the FDAs 10ng/dose requirements.” The FDA ought to be well aware of the potential hazards posed by this DNA contamination, considering its own guidance on DNA in vaccines, published in 2007, states that:¹⁸

“DNA integration could theoretically impact a human’s oncogenes — the genes which can transform a healthy cell into a cancerous cell.
DNA integration may result in chromosomal instability.
The Guidance for Industry discusses biodistribution of DNA vaccines and how such integration could affect unintended parts of the body including blood, heart, brain, liver, kidney, bone marrow, ovaries/testes, lung, draining lymph nodes, spleen, the site of administration and subcutis at injection site.”

FDA Didn’t Perform DNA Integration Assessments

The FDA responded to Ladapo’s letter December 14, 2023, but provided no evidence indicating that DNA integration assessments had been conducted on mRNA COVID-19 shots to address the risks listed in its own guidance document.

As a result, Ladapo is now calling for a halt in their use:¹⁹

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“The FDA’s response does not provide data or evidence that the DNA integration assessments they recommended themselves have been performed.

Instead, they pointed to genotoxicity studies — which are inadequate assessments for DNA integration risk. In addition, they obfuscated the difference between the SV40 promoter/enhancer and SV40 proteins, two elements that are distinct.

DNA integration poses a unique and elevated risk to human health and to the integrity of the human genome, including the risk that DNA integrated into sperm or egg gametes could be passed onto offspring of mRNA COVID-19 vaccine recipients.

If the risks of DNA integration have not been assessed for mRNA COVID-19 vaccines, these vaccines are not appropriate for use in human beings … It is my hope that, in regard to COVID-19, the FDA will one day seriously consider its regulatory responsibility to protect human health, including the integrity of the human genome.”

As noted by board-certified internist and cardiologist Dr. Peter McCullough, Ladapo is hardly alone in this. Tens of thousands of medical professionals and scientists around the world want to see the COVID shots withdrawn from the market:²⁰

“The Florida State Surgeon General’s announcement today is a milestone as more government officials join a chorus calling for recall of COVID-19 vaccines including myself (US Senate, multiple State Senates, EU Parliament, UK Parliament), 17,000 physicians representing the Global COVID-19 Summit, Australian scientists, the World Council for Health, and the Association of American Physicians and Surgeons.”

Resources for Those Injured by the COVID Jab

Based on data from across the world, it’s beyond clear that the COVID shots are the most dangerous drugs ever deployed. In addition to the contamination problem, recent research also shows that flaws in the codon optimization process is causing the shots to produce off-target proteins with unknown health effects and risks.

If you already got one or more COVID jabs and are now reconsidering, you’d be wise to avoid all vaccines from here on, as you need to end the assault on your body. Even if you haven’t experienced any obvious side effects, your health may still be impacted long-term, so don’t take any more shots.

If you’re suffering from side effects, your first order of business is to eliminate the spike protein — and/or any aberrant off-target protein — that your body is producing. Two remedies shown to bind to and facilitate the removal of SARS-CoV-2 spike protein are hydroxychloroquine and ivermectin. I don’t know if these drugs will work on off-target proteins and nanolipid accumulation as well, but it probably wouldn’t hurt to try.

The Front Line COVID-19 Critical Care Alliance (FLCCC) has developed a post-vaccine treatment protocol called I-RECOVER. Since the protocol is continuously updated as more data become available, your best bet is to download the latest version straight from the FLCCC website at covid19criticalcare.com.²¹

For additional suggestions, check out the World Health Council’s spike protein detox guide,²² which focuses on natural substances like herbs, supplements and teas. Sauna therapy can also help eliminate toxic and misfolded proteins by stimulating autophagy.

Five Things New “Preppers” Forget When Getting Ready for Bad Times Ahead

The preparedness community is growing faster than it has in decades. Even during peak times such as Y2K, the economic downturn of 2008, and Covid, the vast majority of Americans made sure they had plenty of toilet paper but didn’t really stockpile anything else.

Things have changed. There’s a growing anxiety in this presidential election year that has prompted more Americans to get prepared for crazy events in the future. Some of it is being driven by fearmongers, but there are valid concerns with the economy, food supply, pharmaceuticals, the energy grid, and mass rioting that have pushed average Americans into “prepper” mode.

There are degrees of preparedness. One does not have to be a full-blown “doomsday prepper” living off-grid in a secure Montana bunker in order to be ahead of the curve. In many ways, preparedness isn’t about being able to perfectly handle every conceivable situation. It’s about being less dependent on government for as long as possible. Those who have proper “preps” will not be waiting for FEMA to distribute emergency supplies to the desperate masses.

Below are five things people new to preparedness (and sometimes even those with experience) often forget as they get ready. All five are common sense notions that do not rely on doomsday in order to be useful. It may be nice to own a tank during the apocalypse but there’s not much you can do with it until things get really crazy. The recommendations below can have places in the lives of average Americans whether doomsday comes or not.

Note: The information provided by this publication or any related communications is for informational purposes only and should not be considered as financial advice. We do not provide personalized investment, financial, or legal advice.

Secured Wealth

Whether in the bank or held in a retirement account, most Americans feel that their life’s savings is relatively secure. At least they did until the last couple of years when de-banking, geopolitical turmoil, and the threat of Central Bank Digital Currencies reared their ugly heads.

It behooves Americans to diversify their holdings. If there’s a triggering event or series of events that cripple the financial systems or devalue the U.S. Dollar, wealth can evaporate quickly. To hedge against potential turmoil, many Americans are looking in two directions: Crypto and physical precious metals.

There are huge advantages to cryptocurrencies, but there are also inherent risks because “virtual” money can become challenging to spend. Add in the push by central banks and governments to regulate or even replace cryptocurrencies with their own versions they control and the risks amplify. There’s nothing wrong with cryptocurrencies today but things can change rapidly.

As for physical precious metals, many Americans pay cash to keep plenty on hand in their safe. Rolling over or transferring retirement accounts into self-directed IRAs is also a popular option, but there are caveats. It can often take weeks or even months to get the gold and silver shipped if the owner chooses to close their account. This is why Genesis Gold Group stands out. Their relationship with the depositories allows for rapid closure and shipping, often in less than 10 days from the time the account holder makes their move. This can come in handy if things appear to be heading south.

Lots of Potable Water

One of the biggest shocks that hit new preppers is understanding how much potable water they need in order to survive. Experts claim one gallon of water per person per day is necessary. Even the most conservative estimates put it at over half-a-gallon. That means that for a family of four, they’ll need around 120 gallons of water to survive for a month if the taps turn off and the stores empty out.

Being near a fresh water source, whether it’s a river, lake, or well, is a best practice among experienced preppers. It’s necessary to have a water filter as well, even if the taps are still working. Many refuse to drink tap water even when there is no emergency. Berkey was our previous favorite but they’re under attack from regulators so the Alexapure systems are solid replacements.

For those in the city or away from fresh water sources, storage is the best option. This can be challenging because proper water storage containers take up a lot of room and are difficult to move if the need arises. For “bug in” situations, having a larger container that stores hundreds or even thousands of gallons is better than stacking 1-5 gallon containers. Unfortunately, they won’t be easily transportable and they can cost a lot to install.

Water is critical. If chaos erupts and water infrastructure is compromised, having a large backup supply can be lifesaving.

Pharmaceuticals and Medical Supplies

There are multiple threats specific to the medical supply chain. With Chinese and Indian imports accounting for over 90% of pharmaceutical ingredients in the United States, deteriorating relations could make it impossible to get the medicines and antibiotics many of us need.

Stocking up many prescription medications can be hard. Doctors generally do not like to prescribe large batches of drugs even if they are shelf-stable for extended periods of time. It is a best practice to ask your doctor if they can prescribe a larger amount. Today, some are sympathetic to concerns about pharmacies running out or becoming inaccessible. Tell them your concerns. It’s worth a shot. The worst they can do is say no.

If your doctor is unwilling to help you stock up on medicines, then Jase Medical is a good alternative. Through telehealth, they can prescribe daily meds or antibiotics that are shipped to your door. As proponents of medical freedom, they empathize with those who want to have enough medical supplies on hand in case things go wrong.

Energy Sources

The vast majority of Americans are locked into the grid. This has proven to be a massive liability when the grid goes down. Unfortunately, there are no inexpensive remedies.

Those living off-grid had to either spend a lot of money or effort (or both) to get their alternative energy sources like solar set up. For those who do not want to go so far, it’s still a best practice to have backup power sources. Diesel generators and portable solar panels are the two most popular, and while they’re not inexpensive they are not out of reach of most Americans who are concerned about being without power for extended periods of time.

Natural gas is another necessity for many, but that’s far more challenging to replace. Having alternatives for heating and cooking that can be powered if gas and electric grids go down is important. Have a backup for items that require power such as manual can openers. If you’re stuck eating canned foods for a while and all you have is an electric opener, you’ll have problems.

Don’t Forget the Protein

When most think about “prepping,” they think about their food supply. More Americans are turning to gardening and homesteading as ways to produce their own food. Others are working with local farmers and ranchers to purchase directly from the sources. This is a good idea whether doomsday comes or not, but it’s particularly important if the food supply chain is broken.

Most grocery stores have about one to two weeks worth of food, as do most American households. Grocers rely heavily on truckers to receive their ongoing shipments. In a crisis, the current process can fail. It behooves Americans for multiple reasons to localize their food purchases as much as possible.

Long-term storage is another popular option. Canned foods, MREs, and freeze dried meals are selling out quickly even as prices rise. But one component that is conspicuously absent in shelf-stable food is high-quality protein. Most survival food companies offer low quality “protein buckets” or cans of meat, but they are often barely edible.

Prepper All-Naturals offers premium cuts of steak that have been cooked sous vide and freeze dried to give them a 25-year shelf life. They offer Ribeye, NY Strip, and Tenderloin among others.

Having buckets of beans and rice is a good start, but keeping a solid supply of high-quality protein isn’t just healthier. It can help a family maintain normalcy through crises.

Prepare Without Fear

With all the challenges we face as Americans today, it can be emotionally draining. Citizens are scared and there’s nothing irrational about their concerns. Being prepared and making lifestyle changes to secure necessities can go a long way toward overcoming the fears that plague us. We should hope and pray for the best but prepare for the worst. And if the worst does come, then knowing we did what we could to be ready for it will help us face those challenges with confidence.