Category: Covid-19 Vaccine Injured New Zealanders

  • 8. Casey’s Story – Spike Protein-Induced Guillain-Barré and a 4-Year Fight for Justice

    8. Casey’s Story – Spike Protein-Induced Guillain-Barré and a 4-Year Fight for Justice

    What started as compliance to protect her dream warehouse job ended in neurological catastrophe, years of medical gaslighting, media smears and bureaucratic battles—culminating in ACC cover approval on August 11, 2025. 

    Casey, 23, suffering a painful seizure

    Before the injection, Casey embodied vitality and joy. 

    “My health was the best that’s ever been. I was working Monday to Friday doing the job of my dreams. I had it all. I loved singing, I was singing all the time, I was enjoying life. You’d find me humming at work. I just remember feeling very content” 

    The jab, administered intravenously instead of intramuscularly by an incompetent vaccinator, triggered rapid onset symptoms: 

    “It took one vaccine for this to happen to me. After an hour I started slowly having symptoms. I had a numb tongue. My body was feeling very off. I collapsed at work. remember crawling to the car.” 

    From the moment her symptoms erupted — numb tongue, spasms, unbearable “ten out of ten” pain and full-body convulsions — she encountered a system primed for skepticism rather than empathy. At emergency care and subsequent visits to North Shore and Auckland hospitals, staff immediately flagged the vaccine link but reacted with reluctance and outright hostility: 

    “They treated me like I was insane.”

    Casey describes how doctors and nurses refused to test or investigate despite visible spasms and vocal tics, as if acknowledging a possible vaccine connection was untenable. In one harrowing instance, during severe episodes where she couldn’t move, walk, or control her body, she was sent to a unit reserved for the dying: 

    “I remember hearing people dying around me. That was very hard.” 

    Isolated and in agony, she repeatedly pressed the call button for basic needs like using the toilet, only to be ignored until she had to crawl across the floor to avoid soiling herself— a stark symbol of dehumanization amid pandemic overload and fear. The dismissal escalated to invalidation when a psychologist, summoned because staff assumed her symptoms were psychosomatic, casually diagnosed her as having “TikTok hysteria.” Implying her suffering stemmed from social media trends rather than a real physiological event, reinforcing the narrative that her pain was fabricated or exaggerated. 

    “I was too busy working to be on TikTok like that. The only thing different is I took a new vaccine, and now I’m like this. What’s going on?”

    Even attempts at treatment backfired: hospitals administered schizophrenic medications and calming sprays that worsened her condition, multiple GPs dismissed her via phone consultations under Covid restrictions. Specialists and ACC reviewers—often deciding without ever meeting her—perpetuated denial, attributing everything to stress she hadn’t experienced pre-injury. It took a compassionate GP who finally reassured her  that “this is happening to you,” and advocated for proper help to break the cycle of gaslighting. 

    “This doctor particularly, he saved my life in a lot of ways. And I will always be grateful for him. I was shaking, I walked in and he looked at me and straightaway knew. Oh, bless him. He helped me a lot. He was able to get me the help I needed.”

    This pattern of disbelief, minimization, and outright rejection not only prolonged her suffering but deepened the trauma, turning a medical crisis into a battle against a system that seemed more invested in protecting the Covid vaccine from disrepute than protecting a harmed patient—leaving Casey to question her reality and sanity as she quickly lost trust in healthcare professionals.

    Media and online attacks compounded the isolation when a Givealittle fundraiser for Casey was labeled a “scam” by immunologist and Deputy Chair of the Malaghan Institute ’s trust board, Professor Graham Le Gros, in aNovember 2021 Stuff article “Covid19: Vaccine experts call for proof as Givealittle scam page stays live.”

    Vaccinologist and Co-Director of the Global Vaccine Data Network, Helen Petousis-Harris, also claimed the Givealittle page Casey’s friend had set up to help her get through her loss of job and severe health problems “should not be seen as evidence that the girl’s symptoms have been caused by a vaccine.” She argued the page should be taken down as Casey should be “applying for ACC.”

    Le Gros said her “symptoms and behaviour are not related to vaccines but to other behaviours and issues” that her claims do not “make medical sense.”

    Helen Petousis-Harris and Graham Le Gros accuse Casey’s Givealittle page of being a “scam”

    “They smeared my character, they smeared my name, they just saw a Givealittle page and just assumed. If you’re going to make comments — come and meet me, come see my life. Come for like a day. See what I deal with!” 

    Casey managed to speak to the reporter, Nathan Morton, who did not retract the story or apologise. But she found a way to forgive them: 

    “I did come to a point where I forgave them, their cluelessness, truly, they had no idea.” 

    After four gruelling years of advocacy, in August 2025, ACC finally approved her injuries: “Injection puncture wound incorrectly administered to the vascular system; Spike protein induced neuroinflammation; induced neurological autoimmunity manifesting as encephalitis with seizures; peripheral neuropathy and Guillain-Barré syndrome; Encephalitis and epilepsy.” ACC’s long-awaited decision brought immense relief.

    “That’s a weight. That’s a whole weight off my back that I’ve been holding for years. Four years, give or take, of fighting so hard just for help.”

    Casey went through four years of advocacy with ACC, before her treatment injury was accepted

    Daily life remains challenging.

    “I still can’t walk properly. Brain fog. I can’t swallow properly. Just simple things like showering or walking to get a letter from the letter box. It’s very interesting having to think about the little things. Make’s you appreciate it.”

    Casey’s amazing spirit endures, helped by her faith and determination. Drawing from Jesus’ teachings, she emphasizes “love and light” amid misunderstanding. 

    “Something that aligned me with Jesus was love and light – within love we can understand, and through light it shines the truth.”

    Her final message is one of perseverance: 

    “Keep fighting. Keep pushing for yourself. Even when you think you’re down, stand back up and fight. My will is stronger than whatever issues I have to face. I’m going to keep going. I’m going to keep fighting.”

    Casey’s testimony stands as another tribute in a growing chorus demanding accountability, informed consent, and compassion for vaccine-injured Kiwis—proving that behind official narratives real lives were damaged, but through sheer will, they have fought the system and won.

    The team at The Tribute wishes Casey strength, joy and continued progress in reclaiming her young life stolen from her.

     Watch Casey’s full episode now on YouTube or Spotify

    Casey struggles to leave the chair, after the interview helped by Lynda Wharton of The Health Forum NZ.
  • 7. Bailey’s Story – Truck Driver’s Pericarditis Event Hours After Jab & Vanishing Records?

    7. Bailey’s Story – Truck Driver’s Pericarditis Event Hours After Jab & Vanishing Records?

    Bailey (25 in 2021), pressured by mandates and a small loan, reluctantly got the vaccine to keep his dream job and new life in beautiful Central Otago.

    “I decided to go, I thought: “Oh yeah, what’s the worst that could happen?” So I went in to the local pharmacy and got my first shot.”

    He was given no warnings about myocarditis or pericarditis – known risks by then for young men, post-Rory Nairn’s tragic death. Rory Nairn had already tragically died from vaccine-induced myocarditis in November 2021.

    En route from Cromwell to Christchurch, the pain hit:

    “I could feel my heartbeat in my throat and out my chest. The pain is a pinching feeling, a shooting pain down your shoulder. Someone sort of grabbing something inside your chest and twisting it.”

    Just six hours after his injection, Bailey pulled over his truck, and was wheeled in on an ambulance gurney to Ashburton Hospital, struggling for breath. Before a single physical examination had taken place, the narrative was already being written. Standing over a man in visible agony, the doctor delivered a verdict that was as much a warning as a dismissal: “Don’t let this put you off the second shot.”

    His mother, Aly, remembers the terror:

    “We had a phone call to say he was in an ambulance. I had begged him not to get it. I tried to say, ‘Come home, let’s ride this out.’ But he was going to lose his job. He was going to lose his home. The pressure was so great.”

    Dismissed and diagnosed with “anxiety” despite clear ECG signs of pericarditis (later described by a cardiologist as impossible to miss), Bailey endured repeated hospital visits across Ashburton, Christchurch, Queenstown,and Nelson. Records vanished: ECGs not uploaded, blood tests “lost,” a cardiac referral “dropped off” the system—a direct violation of the Health (Retention of Health Information) Regulations 1996. Aly launched investigations into four DHBs:

    “One hospital loses records, that’s an accident. But it seems very odd that all of them have lost them.”

     In the presence of Bailey’s fiancée, a doctor issued a chilling verbal warning: “Bailey should never receive another vaccination unless he was positioned next to a crash cart (resuscitation trolley).” Aly wrote to the Christchurch ED doctor requesting that his verbal advice be formally documented in writing, the doctor denied ever having said it. This silence left Bailey in a clinical and legal vacuum; without a written specialist report, he had no evidence to present to the Director-General of Health (Ashley Bloomfield) for a medical exemption.

    Refusing to risk his life, Bailey decided not to take the 2nd shot and he was forced out of his job. Bailey and his partner uprooted back to Nelson, living in his truck during lockdowns, reliant on Nurofen for pain that woke him nightly. “I’ve woken up countless times thinking, am I just going to cark it?”

    As a heavy vehicle driver, he warns of public safety risks.

    “You’ve got truck drivers driving around with heart issues and they’ve just accepted it because no one believes them. They don’t want a bar of it, they just did it to keep their jobs. You know, they’re rough guys, they don’t care.”

    Christmas Eve 2022 brought a breakthrough – a sympathetic ED doctor finally consulted a cardiologist, leading to Bailey’s first formal diagnosis: “vaccine-induced pericarditis.” But relief was short-lived: ACC denied his claim for vaccine treatment injury compensation. Aly and Bailey fought back, and after endless loopholes and reviews, the ICRA finally quashed ACC’s decision in December 2024, approving Bailey for COVID-19 mRNA Vaccine-Induced Pericarditis.

    “It’s a very exhausting process to be dealing with while you’re essentially suffering. No one deserves it.”

    Aly’s OIAs reveal the scale: ACC payouts for vaccine injuries jumped from $145k annually pre-2021 to $11.4m by 2024 (now $18.98m per latest data), with only 1 in 4 claims approved. She also discovered under-40s ED visits for chest pain spiked in 2021 – also matched in Australia, where both countries rolled out vaccines pre-COVID waves.

    Yet the pain persists, Bailey  still suffers three attacks of chest pain every month and remains under the ongoing care of his doctor & cardiologist who has observed that pericarditis in her vaccine-injured patients deviates from pre-Covid norms, and is unresponsive to the typical three-month treatments. For Bailey, it’s an ongoing struggle with heart pain:

    “I probably would have pinned him [my 25-year-old self] against a wall and gone, ‘Don’t do it. You’re going to regret it.’”

    Bailey now begins the ACC Permanent Injury Compensation (PIC) process, 4 years and 2 months after his injury. He faces a system that calculates life in percentages. Aly vows:

    “I’m in this for the long haul. I’m in it for not only my son, but everybody else that was injured as well. It’s so incredibly unjust.”

    THE+TRIBUTE is a web series that gives voice to the Covid jab casualties – the silenced and abandoned.

     Watch Bailey’s full 27-minute episode on YouTube or Spotify

  • 6. Norman’s Story – Pericardial Cyst Injury After One Pfizer Jab

    6. Norman’s Story – Pericardial Cyst Injury After One Pfizer Jab

    With 35 years in healthcare, Norman refused the experimental COVID-19 vaccine rollout based on his virology knowledge and concerns over rushed trials. But New Zealand’s 2021 mandates forced his hand: lose his job in a mental health respite unit, face exclusion from gyms, libraries, and society – or get the shot.

    “I’m not anti-vax. I’ve been a nurse for years, and I’ve probably got more vaccinations than most people. But I didn’t want any of this experimental nonsense put into me.”

    A key theme in Norman’s story is the lack of informed consent amid coercive pressures. He confronted his general manager at work, pointing out the New Zealand’s patient’s Code of Rights, arguing that the mandates are a violation of these as well as fundamental human rights and bodily autonomy.

    “I remember reading out the ten points of the Patient’s Code of Rights, point by point. They’re your rights. It’s not a questionable contract between two people or two groups. It’s your fundamental human rights.”

    The Health and Disability Commission’s poster advertising ten patient’s “Rights”

    Despite his research on Pfizer’s own website highlighting contraindications like prior pericarditis or myocarditis, his attempts to raise these concerns were repeatedly dismissed.

    “I spoke to my GP who knew that I have had viral pericarditis. He should be getting me an exemption.”

    He was told that exemptions from Ashley Bloomfield or Chris Hipkins were unavailable. His GP encouraged him to proceed, promising to support him for any ‘aftermath.’

    At the vaccination center, he again alerted the vaccinator to the contraindication, emphasizing that she should advise against it, but also received poor advice.

    Norman felt his arm was “twisted behind his back.”

    “I’m being kicked out of my society. I’m not going to be allowed to work. I’m not going to be allowed to go to the gym. I’m not going to be allowed to go swimming, go to the library for books.”

    Reluctantly taking one Pfizer dose to audition for a Santa ad, he woke that night with excruciating chest pain – mirroring his experience with viral pericarditis in 2012. Daily recurring episodes followed for 18 months; as well as other symptoms such as breathlessness and an inability to exercise.

    Scans later revealed a large pericardial cyst (5x5x2.5 cm) had formed on his right atrium. Medical consultations have been frustrating, with specialists unwilling to link it directly to the vaccine despite the obvious timing and his history.

    Norman discusses the emotional toll, both positive and negative: job loss, family/friend estrangement followed by joining the Wellington protest convoy, where he found a new community and support among Māori friends.

    “I was embraced by my Māori brothers and sisters. They went “welcome to our world, hello!” Now I’ve been living with them off and on for the past few years, and I have nothing but love and joy and peace and happiness. I’ve got some beautiful friends.”

    He also discusses a profound shift toward living thoughtfully in the present — focusing on gratitude. He emphasises treading softly through life, and chooses to continue to hold a shield and axe for others as he bears witness to issues of human rights, oppression and government overreach.

    Norman’s health is slowly improving, and he is now able to attend the gym every day. Although his heart is not better as he awaits another MRI to look at his heart tissue.

    “It has been nearly a year since my last cardio appointment. Patience is a virtue, so I practice that every day.”

     Watch Norman’s full 20-minute episode now on YouTube or Spotify

  • 5. Vicki’s Story – Learning to Reframe the Journey with a Covid-19 Vaccine Injury

    5. Vicki’s Story – Learning to Reframe the Journey with a Covid-19 Vaccine Injury

    “Before I took the vaccine, I was actually living the life of my dreams. I was doing the work that I loved with a passion. I was really stepping into my gifts, right out of my comfort zone to do that. But I felt like I was flying.”

    In her late 50s, she discovered forest therapy, a therapeutic practice born in Japan known as shinrin-yoku or forest bathing. Training in the United States as one of the first guides outside Japan and the US, she brought this gentle art back to New Zealand.

    “I love to go out into nature and just be present with it and to discover the beauty and the joy in the little things.”

    She watched it grow, mentoring others and leading sessions that encouraged presence with the natural world. When COVID-19 hit and vaccines rolled out, Vicki felt the pressure in her tight-knit community. The head nurse framed it as now or never, and travel, a cornerstone of her work, seemed impossible without it. Despite a history of chronic fatigue syndrome (M.E.), which made her immunologically vulnerable, public messaging insisted people like her needed the jab. Her homeopath warned against it— but Vicki felt healthy and able.

    “I thought, right, okay, I’m just going to go get this done. And at that stage, I was feeling probably the most well and healthy that I had felt in years.”

    She got the shot on May 28, 2021. A few days later, headaches and brain fog set in. Ten days post-vaccination, while teaching online, disaster struck.

    “I looked at my page and things were not making sense. I was reading words, but there was complete brain confusion around them. It was just a very odd sensation. And I didn’t know where the heck I was. I didn’t know what I’d said. I lost all memory of the whole morning that had preceded this, and I was in a state of total confusion.”

    Her US colleague suspected a stroke, took over the Zoom class, and coached her for three hours until help arrived. Vicki was helicoptered to Auckland Hospital with blood pressure at 200 over 125. Doctors suggested she had experienced a transient global amnesia episode. From there, her health deteriorated into central nervous system dysfunction: headaches, body pain, chronic fatigue and more.

    The changes were profound. Vicki had to step down from online teaching due to screen triggers. She now does limited in-person mentoring, planned around low energy as her body craves rest.

    “I still find I have quite a lot of resistance to living a life that’s horizontal, because that’s actually what my body wants to do all the time. I still have such a zest for life. I can’t lose that. I’ve been down the bottom of the rabbit hole with this and got very depressed and incapacitated — it was like my whole world had closed in, and I ain’t going to go there again.”

    Vicki chose to reframe her ordeal not as defeat, but as an invitation for profound inner work. The enforced stillness allowed for deep meditation she had previously skimmed over in her busy life, and she also chose to foster tenderness and self-care. She is learning to listen to her body.

    “I’m still learning how not to push myself through to getting tasks completed. That’s a difficult thing for me, if I start something, I want it done. And my tendency is to push through and then I just crash, I collapse. So it’s a process of learning to listen and say, ‘Okay, you need to go sit down now.’ And giving myself permission to do that.”

    Nature remains a lifeline and her sanctuary.

    “One of my strategies is going out into nature. Getting my feet in the ocean. Starting my day off with that is just the best thing I can possibly do. Even taking a quick dip, like a skinny dip when no one’s around, it just really revitalizes my whole body and gives me that sense of, ‘wow, life is amazing’, even if it’s only fleeting. But I know it’s there and I know it’s possible.”

    She delved into neuroplasticity and psychoneuroendocrinology, retraining her brain to diminish damaged pathways and bolster those promoting hormonal balance and well-being. Spiritually, it became a quest for grace amid suffering, moving through pain without denial, and using it as a catalyst for growth. She consistently works to reframe the experience.

    “I’ve always had this thing inside me that knows there is more to life than this body. There’s more to life than just the things that happen to me. I have this strong desire to, not only survive, but to thrive. And I have been in survival mode, but to thrive and, to find my joy. Because I see so much beauty around me. And I think life is a gift—it really is.”

    Through it all, Vicki unearthed new gifts in adversity. She learned to receive help, balancing her empathic giving nature. Digging deep, she affirmed her soul’s evolution, while holding space for others’ as well.

    “It has provided an opportunity to dig really deep to get to the essence of me, who am I? What am I here for?”

    Vicki calls for accountability: vaccine exemptions for any reason, compensation for ongoing costs—she spends hundreds monthly on health, now unsustainable without income—and she wants an apology. 

    “I would like the government and the Ministry of Health to apologize. Just accepting some responsibility. And I think that would go a hell of a long way for many of us. Just saying sorry—we got it wrong.”

    Today, Vicki continues on a slow but steady path forward. It’s a gradual process to see lasting gains in her physical health, but she is experiencing meaningful improvements in her mental well-being. She focuses increasingly on brain retraining, neuroplasticity, and mind-body approaches, supported by helpful online groups. 

    “There is really good science behind this about how and why this works for many of our chronic wacky issues that the average Medics have no answers for.” 

    She understands her symptoms as signals from a dysregulated nervous system—triggered by the vaccine and stuck in chronic fight-or-flight—rather than enemies to fight. Acceptance, deep self-listening, compassion, and allowing joy guide her daily life now. At 67, old habits shift slowly, but she takes gentle, tentative steps on this healing journey.

    Vicki reflects on sharing her story: 

    “I want to thank you again for your willingness to share my story through video – it was a pivotal experience for me to speak my truth that day, to be truly listened to and to begin to take charge of my ongoing recovery journey.”

    The team at The Tribute wishes Vicki strength, peace, and continued progress in reclaiming her life.

     Watch Vicki’s full episode now on YouTube or Spotify

  • 4. Adyn’s Story – A Teenager with High Platelets and Thrombosis after Covid-19 Vaccination

    4. Adyn’s Story – A Teenager with High Platelets and Thrombosis after Covid-19 Vaccination

    His story exposes how the fear-inducing propaganda of the Covid-19 response left a young teenager feeling in terror of catching Covid, along with fears around his newly diagnosed Essential Thrombocytemia with its potential blood clots and uncontrolled bleeding.

    Adyn was a young, healthy active student at Boys High in Christchurch, who prioritized friends, football and fitness over everything.

    “I was quite healthy. I always picked spending time with friends and family over anything else. I just wanted to be out and about.”

    He received early access to the vaccine as his stepdad was high-risk. The process felt surreal—like a military operation with MPs present and a strange sense of ceremony.

    “It was like a military base. I felt famous almost. I felt like I was graduating high school.”

    What began as a routine jab for Adyn in early 2021 quickly spiraled into a health crisis that isolated him from friends, family and normal teenage life. Symptoms hit fast. Within 40 hours: blurry vision, violently shaking hands turning purple, brain fog so severe he couldn’t focus or even recall his classroom. His skin flared—eczema returning worse than ever, extremities feeling icy while his core burned.

    “My hands were shaking a lot. I basically just kept shaking, like very violently. I thought I was going to rip the page out of the book. Then my hands went purple.”

    A quick visit to the doctor, 45 hours after his vaccination, spotted unequal pupils, and a clot was suspected. Blood tests 13 days post-vaccination revealed platelets at 967,000—double the healthy max of 450,000. Counts kept climbing past 1,000,000.

    “Normally someone would have about 150 to 300 of these, and the maximum is 450, and mine was far above that.”

    Platelets, produced in bone marrow alongside red and white cells, clump to seal damaged vessels, stopping bleeding and aiding healing. But extremes bring opposite dangers: Adyn was given terrifying warnings that levels near 1,500,000 risked catastrophic bleeding.

    Diagnosed initially with leukemia by a hematologist, he was devastated. “I thought I had five years to live,” he recalls. Further tests clarified it as essential thrombocythemia (ET), a blood disorder where bone marrow overproduces platelets. Though rare in youth, the timing—the devastating symptoms starting immediately after vaccination—eventually convincing him, his family and GP of a link.

    “It happened directly afterwards.”

    Cognitive issues also continued to worsen: slurred speech like a stroke, drooling and anxiety. Deemed “high-risk for COVID” because of his vaccine-induced condition, Adyn isolated himself, building metaphorical “walls” and a “ship” to cast himself away from friends and family. He lived in fear, confining himself to his room for six months post-lockdown.

    “I told all my friends that I had to be away from them. I couldn’t go near them. My family as well. I just thought if I went outside, I’d catch Covid. I thought it was kind of, like, looming through the air. It was quite scary because I thought with my condition, if I was to get Covid that would be the end of it.”

    Treatment was grueling. Chemo pills caused muscle loss and weight drop to 66kg, making him fear that would kill him faster than ET. Switching to expensive interferon (Pegasys) injections brought platelet counts down to 500-600, and boosted his energy and immunity. He’s now in remission, monitored annually. Adyn explains that he’s likely caught COVID five or six times but recovered easily, finally realising his fears were amplified by over “dramatised” messaging.

    Once I realised that a lot of my friends were safe, even though they were out and about. And that the people who caught it got over it pretty fast. That helped ease my nerves a bit.

    A 2022 systematic review of studies of over 125,000  children and adolescents  reported high prevalence of COVID-19-related fear, as well as mental health deterioration, such as depressive and anxious symptoms due to COVID‐19 pandemic control measures. Those with chronic physical conditions were more likely to experience negative mental health outcomes.

    Adyn explains how applying for ACC (Accident Compensation Corporation) was a battle as his blood specialists denied vaccine links. However, a supportive GP advocated for him, highlighting the 13-day platelet spike, instant neurological conditions and thrombocytosis, leading to an ACC medical claim acceptance. They reimbursed his costs, including interferon, but denied a lump sum, as his hematologist wouldn’t confirm causation.

    “It didn’t feel like they were human, it kind of felt like they were just talking off of what they’ve been told to say. And they weren’t open to any different opinions at all.”

    According to a proactive release from ACC of Covid-19 vaccine related treatment injury claims, total payments on 1,779 accepted claims currrently amount to $16,877,835 —including 6 claims which relate to a fatal injury.

    Adyn’s schooling suffered; after difficulties studying from home, finally entering class proved challenging. He dropped out in Year 13 to pivot to training for fitness coaching. 

    Today, in his early 20’s, Adyn’s now a personal trainer, embracing life even though he explains his ET carries a 1% risk of mutating to aggressive leukemia. 

     Support from family and his ex-partner was crucial:

    “It wasn’t really exactly the things they said to me. It wasn’t me hearing a specific thing, but it was just knowing that those people are always looking out for you. And there’s always someone who cares about you.”

    This experience flipped his worldview. From feeling invincible to experiencing rock bottom, he now appreciates health and relationships. Declining further vaccines, he urges self-care without taking well-being for granted. For those in similar “ships,” his message: Keep your head up—land awaits.

    “Just enjoy life as much as you can..”

     Watch Adyn’s full 20-minute episode now on YouTube or Spotify