Covid vaccine injured - Silent no More

Was taking the Covid vaccine Worth a Shot? A new book by Caroline Pover, written on behalf of Brianne Dressen who lives in the USA, chronicles the horrific story of how she was severely injured by the Covid vaccine after enrolling on the AstraZeneca trial in November 2020. Caroline sensitively and professionally tells the heart wrenching, eye-opening account of how Brianne Dressen’s life was turned upside down and irreversibly changed forever the day she chose to volunteer to enroll on the UK-led AstraZeneca clinical trial. This book takes the reader along the rollercoaster ride of the devastating injuries caused by the vaccine and the blatant abuse of power by the healthcare system to denigrate, ignore, and cover up her injuries - along with many others labelled - as ‘misinformation’ spreaders by the medical-industrial-military complex. Every person on the planet was misled by governments, NGO, regulatory agencies, corporations, Big Pharma, healthcare professionals, along with social and mainstream media. From how clinical trials are conducted to the lack of injury compensation, wide scale censorship, corruption and abuse of power, this book shows the myriad ways Brianne fought and continues to fight for truth and justice for the Covid-vaccine injured, who have been completely abandoned and often maligned by society.

The AstraZeneca Clinical Trial

In the introduction, Caroline Pover describes how she had been medically diagnosed with an adverse reaction to the Covid vaccine and was led to believe Brianne Dressen did not exist. It was only when she started posting on social media and heard about another woman who was dropped from a clinical trial because of an adverse reaction to the vaccine, that their paths crossed. Worth a Shot is a book based on real events that impacted on real people and is a narrative account of Brianne’s (Bri’s) story containing brutally honest struggles with how her life has changed irreversibly after the covid vaccine, including her plans to contemplate suicide. Bri had the perfect life: she was a fit, active lady who always pushed herself physically and mentally. She had a wonderful family life, married with two children with a dream house in the mountains. After having children, Bri set up her own preschool to help children who struggled in a typical educational environment. Then in 2020, Covid hit!

When the lockdowns happened and the talk of vaccine trials began, Bri wanted to help in anyway possible with contributing to scientific advancements; once “Operation Warp Speed” was being regularly reported in the media, coupled with her husband’s scientific background, Bri felt excited to enrol in the new Covid vaccine trial set up by Oxford University in conjunction with AstraZeneca, which was recruiting in UK, Brazil, South Africa, and the USA. The opening in the USA was in Salt Lake City - just 40 minutes drive from Bri’s home. She had a phone interview with a trial representative for several hours to capture her medical history and was considered an excellent candidate for the trial. Things then went quiet, but out of the blue on 4th November 2020 - the day after the election - she was called into the trial. The consent form she signed was very thorough. It went through all the expectations and explained it was a double-blinded study and that so far 5,000 individuals had received at least one dose, and the side effects were mild to moderate but transient in nature. It also stated that if anyone did experience an adverse reaction they might be withdrawn from the study, but any medical treatment needed for reactions would be covered by AstraZeneca’s insurance policy. Bri took the vaccine, but tingling started within an hour of the injection.

Adverse Reaction

Bri’s reaction was severe. Tingling spread from below her right elbow all the way up her arm and shoulder, then to the other arm. The tingling got progressively worse and her eyes started to blur, and she saw double. Her hearing started to go muffled, but she assumed the symptoms would be gone by the next morning. However, her symptoms intensified, and now both legs were becoming weaker. She called the number on the consent form to report her reactions, but no one answered her call. Within days, she was confined to her bedroom, with drapes covering the window to shut out the light. Within weeks, her condition worsened so she saw a neurologist and visited an out-of-hours emergency clinic. Nausea, vision disturbances, tingling, extreme sensitivity to sound, limb weaknesses, as well as excruciating pain developed all over the body, including her teeth, stomach, bones, joints, legs and arms. She could not eat and lost 20 lbs within weeks. Her body seemed to vibrate and buzz from within constantly, and she could not bear anyone touching her, with extreme sensitivity to sound, light, and food. She spent weeks then months confined to her bed. She lost control of her bladder and her blood pressure was erratic. None of the pain medications helped.

Her husband and other family members and close friends helped with looking after the children and caring for her. Yet Bri and her husband did not want to broadcast these issues publicly when so many were struggling with Covid itself. Weekly and even sometimes daily visits to the hospitals baffled the doctors. Friends visited her but the visible transformation of her appearance shocked them, and she had to wear earplugs and sunglasses. Attempts at exercise were futile, as the pain was too unbearable. She visited multiple experts but to no avail. The principal investigator of the clinical trial suggested she might have multiple sclerosis (MS), but the trial clinic did not recommend any other specialists. Local neurologists recommended she visit the ER. The clinic staff told Bri that the ramifications were serious if she thought there was any possibility the vaccine had caused these symptoms. When she said her reactions were from the vaccine as she was a trial participant, most professionals were not interested and dismissed the symptoms as Covid. She had MRI scans but found nothing significant; there was nothing they could do. Bri was to report back to the trial clinic, which she did. They told her not to worry because AstraZeneca would reimburse all her medical costs - and they would be in touch soon. But no one contacted her.

No Diagnosis

She continued to go through the proper channels and medical experts to get answers. After a series of tests that ruled out MS and other neurological conditions, she was no closer to a diagnosis. By ploughing through scientific papers and doing their own research, Bri discovered post-vaccination transverse myelitis (TM), Guillain-Barre Syndrome (GBS) and acute disseminated encephalomyelitis (ADEM). Both TM and ADEM are conditions relating to inflammation of the spinal cord or central nervous system, which can lead to permanent damage. Despite Bri reporting this to the trial clinic, the trial was not put on hold. She was told to report everything back to AstraZeneca, which she did, but despite all the assurances, no one contacted her. Bri’s multiple trips to the hospital caused by the vaccine meant she was a burden to the healthcare system. Many physicians shrugged off her symptoms as psychiatric because none of the tests produced any explanation. She was put on antidepressants and gabapentin for neurological pain. Nothing had been put in place to deal with anyone who had an unexpected reaction to the vaccine.

On the next visit to her clinic, Bri hoped someone would be able to help her with her condition but was told no one could see her unless she signed a new consent form. She asked what was different about this form but they insisted they could not help her unless she signed it. Bri’s vision was so impaired that she could not read the form. She felt she had no choice but to sign it. Once she signed the form, two nasal swabs were taken and a blood test to confirm she did not have Covid, and she was discharged. Bri reached out to the CDC, and her husband filled out a VAERS report, but no one responded. Bri’s health deteriorated and the medical costs were mounting up, with assurances AstraZeneca would reimburse. After weeks of scouring the internet they discovered that IVIG (intravenous immunoglobulin) might be a possible treatment. When they showed this to the doctors and other experts, they were ignored and refused this treatment. The only interaction from AstraZeneca (via a third party) was that Bri was ‘unblinded’ from the trial at her request as she wanted to know if she had received the vaccine, which was later confirmed. The trial sponsor agreed she would not receive a second dose, but they offered no help or support about her continued deteriorating health.

Losing Hope

Exhausted and losing hope, Bri and her husband reached out to the NIH. They were surprised when a specialist neuroimmunologist, Dr Avinthra Nath, Director of the National Institute of Neurological Disorders and Stroke at the NIH, and a researcher at the National Institute of Allergy and Infectious Diseases (NIAID) who worked directly under Dr Anthony Fauci, responded with interest to learn more about Bri’s condition. An appointment was arranged and he seemed very sympathetic and gave the impression he was keen to help. Bri then learned the shocking news that the AstraZeneca vaccine was authorized for use throughout the UK. Publicly the trials were being celebrated as hugely successful, but Bri knew otherwise. She felt suicidal - she was a climber, skier, and dancer who was now a completely non-functioning member of the family barely able to leave her bedroom. Bri’s circle of friends started to diminish. Their savings were also being rapidly depleted because of the skyrocketing medical costs. What about all the assurances on the consent form? What happened to all the promises of the costs being reimbursed? Bri began to lose hope. A trip into nature with her sister that aimed to be a temporary distraction for her resulted in a candid but dark exchange. Her sister asked her to promise her not to kill herself. Bri replied “I cannot promise you that”. The chapter describes how she planned to take her own life, so she was less of a burden to her family. Mercifully, she changed her mind and instead directed her focus on finding and helping others who might be injured and experiencing the same nightmare she was going through.

The Many Injured

It didn’t take long before Bri joined support groups online. After some time she saw a posting from another lady who was also injured in the AstraZeneca trial. Finally, she could talk to someone who knew exactly what she was going through! Within a few days she found another clinical trial participant (Moderna trial) who also experienced similar debilitating reactions. In this patient’s case, she had her left lymph nodes removed as they were so swollen but she became bedridden owing to complications of the surgery. Bri befriended Dr Danice Hertz, a retired gastroenterologist who had developed Mast Cell Activation Syndrome (MCAS) following the Pfizer jab and was suffering ongoing allergic-type reactions including tinnitus, chest pains, and severe nerve damage to her face. Danice increased the number of patients referred to the NIH and Dr Nath for his study. Soon she was inundated with emails from others who had experienced adverse effects from covid vaccines. Sheryl Reutters was harmed by the Moderna jab, experiencing a severe neurological reaction, and soon became a close friend of Bri. Mary Johnson a front-line ER and critical care physician who was injured by the vaccine, and was driven out of her job and confined to her home. Kristi Dobbs and Candace Hayden were also damaged by the vaccine. Bri trusted the NIH to take care of all these injured and would talk to them each week to learn about their stories.

The number of people with vaccine injuries kept mounting and they were all being ignored by doctors and the drug companies. So, the group decided to create a Covid vaccine injury support group on Facebook. However, anyone publicly criticising the vaccines soon became labelled as ‘conspiracy theorists’ and more prominent healthcare workers with dissenting voices became known as the “Disinformation Dozen”. After taking a default position of always giving the benefit of the doubt, Bri was now beginning to realise they had been strung along for months. Her own children were starting to struggle at school, and were developing anxiety, and her son was afraid of leaving the house. Then Bri discovered Maddie, a 12-year-old girl who was completely healthy before receiving the Pfizer vaccine, who was left unable to walk or eat, incontinent, and with seizures and fainting episodes. Bri and the core group of vaccine injured decided enough was enough - they had to go public!

Going Public

They started to post their testimonies and videos about their experiences on the website; some of the stories were harrowing. The videos found their way onto TikTok and were receiving millions of views, as traffic to their website exploded, with over 300,000 views per week. More and more stories poured in from around the world. Facebook seemed to be where many of the support group interactions were residing. By early 2021, although Bri had yet to find anyone else injured by the AstraZeneca jab, in the UK reports of blood clots were flooding in. Slowly news reporters began contacting them and they promised to cover the stories of the vaccine injured along with statements from governments and drug companies. The group reached out to the CDC, FDA, and VAERS but no one received a significant response. How many others were out there with the same relentless pain, alone and with overpowering thoughts? Petitions were submitted to the FDA, CDC, VAERS, and the White House, after one lady who was part of the injured group took her own life. They went to the top, and contacted Dr Peter Marks, Director of the Centre for Biologics Evaluation and Research at the FDA. Word was now spreading among the vaccine-injured community that the NIH had been contacted about hundreds of people with adverse reactions.

Bri and her newfound friends detected a distinct unease among most doctors and nurses whom they engaged with during their multiple visits to the hospital. Bri spent a week at the NIH having multiple tests, which confirmed she had nerve damage in her legs and autonomic nervous system issues. She was diagnosed with “post-vaccine neuropathy”, and recommended IVIG therapy - the very treatment Bri had pleaded with the doctors to try but were ignored. One of Bri’s friend’s, Casey, was an NIH employee who had suffered severe neurological complications as a result of the vaccine. Casey met with Dr Nath, who had previously reassured them that they were documenting and researching all the injuries. When Casey then confronted Dr Nath about his research he flatly denied any such research was underway even though Bri had spent a week at the NIH having tests and being placed on the IVIG protocol. They had no choice but to get political, so they arranged a call with Wisconsin’s Senator Johnson who had been outspoken about the harms caused by the covid vaccines and the censorship, and had been critical of the lockdown policies. Bri was cautious of accepting Senator Johnson’s help because of how he had been portrayed, but on meeting him found he was full of kindness and willing to expose himself to attack on their behalf.

Senator Johnson agreed to hold a press conference. The vaccine injured community felt the politicisation of their health and ‘vaccine stance’ was very draining. One of the support groups that came together with Bri’s group was named “A Wee Sprinkle of Hope” to reflect the culture of compassion. The real objective of the vaccine injured movement was to help people who were suffering. No headline news from the press conference was on the mainstream media, it was mentioned as an aside before going to the next item. Every vaccine injury was not misinformation and their abandonment by the manufacturers was not misinformation. Instead, the news reporters centred the stories not around the vaccine injuries, but around the fact it was led by what they claimed was a crazy, right-wing ‘conspiracy theorist’: Senator Johnston.

Censorship

Then the censorship started. Within 24 hours of the press conference, Facebook began shutting down the support groups. The injured gathered together and then joined with A Wee Sprinkle of Hope. Thousands had joined, and the group was getting larger by the day. Then 5 days after the press conference, and without warning, Facebook shut down the largest Covid vaccine injury support group in the world. Now the injured could not even talk to each other! The social media platform was actively restricting people suffering from extreme physical and emotional pain from communicating with each other. Soon the group decided to develop code words so they could still communicate under new names. Then a mainstream news article exposed one of the code words, and a new group of 30,000 members was shut down too! Warnings appeared beneath people’s posts on their own pages urging viewers to go to Facebook's Community Guidelines on ‘accurate’ information about vaccines. The warnings also deterred other Facebook users, suggesting they should not interact with ‘repeat offenders’ posting misinformation about vaccines. People’s posts were also being ‘shadowbanned’ or hidden by Facebook algorithms.

Bri was eventually paid a measly $590.20 from AstraZeneca, which coincided with her learning of other injured people in the UK in early 2021. The injured were getting mixed messages from the NIH. On the one hand, they were paying for people’s tests and diagnosis, but then they denied any research was being done. Eventually Dr Nath stopped responding to emails and the FDA stopped communicating with Danice. The NIH then shut down the entire study of the covid vaccine injured and cancelled Bri’s upcoming trip to the NIH. Some of the “Disinformation Dozen” also had their social media accounts shut down or restricted. By now, authors, doctors, patients, activists and even celebrities were being censored. Bri’s husband studied all the clinical trial study reports that had come out, matching the injured participants they knew of to the recorded reactions and found most had been downplayed or even omitted.

It was becoming clear that the institutions they had previously trusted, such as the media, science, pharmaceutical companies, and the government were hiding the truth or outright lying about Covid vaccine adverse reactions. They were being silenced. Free speech was officially over. But another threat was looming: vaccine mandates! The idea of mandating Covid vaccines was terribly distressing to many of the injured. They knew first hand that no one would be there for anyone if they developed a severe reaction. Being fully vaccinated meant you could go to work, visit restaurants or travel without restriction. Those same ‘privileges’ would not be open to the unvaccinated. The coercion, propaganda, bribes and incentives to get the vaccines was extraordinary. Next they were going to jab children.

Eventually, Bri discovered Dr Doshi, an Associate Professor at the University of Maryland with an interest in the drug approval process and an expert in clinical trials, who was also a Senior Editor at the British Medical Journal. Bri and others set up a call with him, and he suggested organising a roundtable discussion in Washington, with senators, health officials and all media. Other pharmaceutical policy experts were brought in, and Bri and her friends started to gather the vaccine injury testimonials. Fundraising was needed to pay for the injured to travel to the event. Some organizations donated together with crowdfunding efforts that raised £37,000 to pay for everyone's travel and accommodation. The roundtable event at the Senate lasted over 4 hours, which sparked some media interest. The clinical trial company offered a single ‘full and final settlement’ payment to Bri of £1,243.30. This amount did not even cover one-half of the cost of a single IVIG infusion. It seemed the second consent form that Bri had signed (under duress) had significant changes that included all the symptoms she had suffered since the jab, effectively invalidating the previous consent form. After meeting another vaccine victim, Dr Joel Wallskog, Bri and others formed a new group: React19.

Going Global

A Pfizer Whistleblower, Brook Jackson, had been a regional director at one of the clinical trial sites and expressed serious concerns about how the Pfizer Covid vaccine trial was conducted. Despite the stories some mainstream channels promoted about vaccine misinformation and “anti-vaccine propaganda”, clips of the roundtable event were going viral. Many of the vaccine injured, including healthcare professionals and doctors were risking their careers by speaking out against the vaccines. While React19 was originally set up to support the American’s who were injured, it ultimately became a hub for the vaccine injured all over the world. What became clear was that vaccine injury support groups before the covid vaccines faced similar medical gaslighting. The difference this time was never had a vaccine been administered to so many people at the same time - an estimated 5 billion globally - so the global repercussions would be huge. A chat group was initiated for React19, which grew with international leaders, creating a unified effort. Charlet Crichton set up the UK-based UKCVFamily around the same time as React19, as the healthcare system in the UK is different to the USA and more people in the UK had been given the AstraZeneca vaccine. Both groups now collaborated.

It was also becoming clear that as the vaccine injured community grew, the adverse reactions in all the trials had been hidden or misrepresented. Throughout her journey, Bri had started out searching to find the support she needed, but since taking on a leadership role in React19 she was now the support. The end of the book chronicles how finding allies was not as easy as some might assume. There was still no research paper from Dr Nath from the NIH, and when it finally did materialize on a preprint publication, it only published data from 24 patients (despite having over a hundred cases). Furthermore, any links to the adverse events of the vaccine were completely downplayed. When the injured were invited to speak at events by ‘advocates’ on behalf of the injured, often it was more for appearances. Some people in the freedom movement wanted to raise their profile through association with the vaccine injured, but were not directly offering help. Gradually the environment changed so that it was more ‘acceptable’ to discuss vaccine injuries. The film produced by Mark Sharman (former ITV and BSkyB News Executive) “Safe and Effective: A Second Opinion” released on YouTube in October 2022, was removed from the platform within hours following its mention in a Parliamentary debate, despite amassing over a million views!

Find the Science, Find the Money

The immunization surveillance systems such as VAERS, Yellow Card report scheme and others were not working. It is estimated fewer than 1% of adverse reactions are even logged on these sites and so the true nature and scale of such reactions are far greater than captured on these systems. A staggering statistic of the VAERS system is that in the 30 years of vaccine injury, 50,000 reports had been logged. In 2021, there were 750,000 reports of adverse reactions. In other words, the covid vaccine reports in 1 year outnumbered all adverse event reports from the prior 30 years combined. Many of the VAERS reports were not being followed up or being processed properly. Studies submitted to journals that had any data that questioned the vaccines, were often rejected from multiple journals.

Compounding the issue, the 1986 US National Childhood Vaccine Injury Act (NCVIA) removed any financial liability from the manufacturers if any deaths or injuries were caused by vaccines. Moreover, vaccine damage payment schemes, such as the VICP in the USA, were wholly inadequate as proving vaccine was the cause meant hardly any claims were successful and any moderate payments often took years. The PREP (Public Readiness and Emergency Preparedness) Act established in 2005, also granted pharmaceutical companies immunity from federal or state litigation, in circumstances such as a pandemic. So, the companies making the vaccines have no responsibility for damage and little if any incentives to carry out scientific research into any injuries caused. The vaccine injured had to find the “science to follow” rather than “follow the science”. A combination of the “fact-checkers” who demolished any “anti-vaccine” testimonials and that medical reimbursement was non-existent, the out-of-pocket medical expenses the vaccine injured faced often exhausted personal savings to the point that many were refinancing or selling their homes.

Conclusion

The fear-mongering that had contributed to many of those injured by the vaccine to choose to get vaccinated in the first place was now continuing for this marginalized section of society. Those injured by the Covid-vaccine also learned from people who had been injured by past vaccines. The censorship tale was all too familiar, but the React19 community started doing their own research and discovered alternative therapies - be it pharmaceutical, natural, physical, spiritual - and lifestyle adjustments could help with their symptoms. The Covid vaccine rollout left a trail of devastation and damage in its wake. Social cohesion and disconnection also set in with the vaccine-injured ostracised from society. Whether vaccinated or unvaccinated, most people have been affected by the loss of relatives, friendships, relationships, and often life-long careers and financial autonomy. For many, finding support in such dark times has literally been the difference between life and death. We all need healing from the collective trauma of the Covid era, which is still ongoing. By sharing this poignant story of the many Covid-vaccine injured, we hope this will inspire more kindness, connection, compassion, and courage to be open about the truth. That is Worth a Shot!

Worth a Shot?: Secrets of the Clinical Trial Participant Who Inspired a Global Movement―Brianne Dressen's Story, told by Caroline Pover, was published in November 2024 by Skyhorse Publishing, New York, ISBN: 9781510783461.

All proceeds from the book go to UKCVFamily and React-19, support vaccine -injured in UK and worldwide.