Eight-year-old Richard Jeferson Bustamante Bautista has had a horrific reaction to the Pfizer COVID Vaccine.

He received the first dose on January 30, 2022 and the second dose on February 21, 2022.

A few days later he developed “Stevens-Johnson Syndrome” and is currently hospitalized.

[TRANSLATED]

He had a reaction three days after his 2nd Pfizer dose. He had hives all over his body, and has been in two different hospitals since. He’s currenly in a children’s hospital in Lima, being treated in the burn unit for his skin condition.

He is progressively getting worse.

The father didn’t know the vaccine was experimental, and was all but forced into giving it to his son as there was the threat of him not being able to attend classes without it.

His sight is suffering and he needs an operation currently because he cannot urinate.

Cody Flint – 33 Year Old Pilot with over 10,000 flight hours.

In February, he got his first Pfizer vaccine.  Two days after his initial reaction to the vaccine, he got in his airplane, and that’s when things took a horrific turn.

Clint’s testimony given in Washington DC on November, 1st, 2021 is below.

“I received the first dose of Pfizer on Feb. 1 [and] within 30 minutes I developed a severe, stabbing headache that later became a burning sensation in the back of my neck.

Two days after vaccination, I got in my airplane to do a job that would take only a few hours. Immediately after taking off, I knew something was not right with me. I was starting to develop tunnel vision and my headache was getting worse. Approximately two hours into my flying I pulled my airplane up to turn around and felt an extreme burst of pressure in my ears. Instantly, I nearly blacked out; dizzy, disoriented, nauseous, and shaking uncontrollably.

By the grace of God, I was able to land my plane without incident. Although, I do not remember doing this.

[I was diagnosed] with left and right perilymphatic fistulas, eustachian tube dysfunction, and elevated intracranial pressure due to brain swelling. My condition continued to decline and my doctors told me only an adverse reaction to the vaccine or major head trauma could have caused this much spontaneous damage. I’ve had six spinal taps over eight months… and two surgeries, eight weeks apart to repair the fistulas.

I have missed nearly an entire year of my life and my children’s lives.

My days have been replaced with being trapped in a sick body, doctor visits, invasive procedures, and more questions than answers.

I don’t know if I’ll ever be able to fly an airplane again.

This vaccine has taken my career from me and the future I have worked so hard to build. I have used all my savings to pay medical bills and to just be able to survive. My family and I are on the verge of losing everything we have.

The FDA, CDC, and NIH refuse to acknowledge that real lives are being absolutely destroyed by this vaccine. 

His video testimony is below.

Watch the entire testimony given in Washington DC on November 1, 2021 below.

Florian Dagoury, the world’s top static free diver was just diagnosed with Myocarditis and Pericarditis, just 40 days after his 2nd Pfizer Vaccine dose.

Here is the information from his Instagram page:

“Just want to share my annoying experience after vaccination and perhaps have some testimonials from similar stories amount Freedivers. Did you get better?

After my 2nd dose I noticed that my heart rate was way higher than normal and my breath hold capacities went down significantly. During sleep I’m at 65-70bpm instead of 37-45bpm. During the day I’m now always over 100bpm instead of 65bpm, even when I sit down and relax. Once I even reach 177bpm while having dinner with friends !!!!

10 days after my 2nd jab, I went to see a cardiologist and he told me it’s a commun side effect of Pfizer vaccin, nothing to worry about, just rest it will pass.

40days after 2nd jab, I had no progress so I went to see an other cardiologist and got diagnosed with Myocarditis and Trivial Mitral regurgitation! Which is basically an inflammation of the heart muscles cause by the immune system and some tiny leaks of blood from the valves that no longer close properly. I’m now struggling to reach 8min breath hold, 150m dyn and I even have a strong urge to breath doing 40m dives. 30% decrease on my diving performance roughly.

My first thought and recommendation to Freedivers around the world is to chose a vaccin which is done the old fashion way like Sputnik, Sinovac, Sinopharm etc…instead of those new mRNA vaccins. “

Leah Edgar, a healthy and happy mom of a toddler.

On May 9th, 2021 Leah had her first Pfizer COVID Vaccine Dose.  Her reactions to it started within 24 hours.

Here is her story:

My life and health forever changed on May 9th, 2021. Sadly I didn’t listen to my gut and let the pressures of my workplace, as an educator, get in the way of making the choice.

Immediately after receiving it I knew something was wrong, I started having visual disturbances. Later that evening a huge welt to appeared on my back. It was painful I went to the hospital and they could give me no explanation other than it was potentially shingles caused by the you know what. Following day I started having chest pains, palpitations, dizziness and vertigo. This went on for months, as well as having issues with my temperature, tolerating heat, having flares where my cheeks would burn hot as fire and related to be described as ongoing allergic reactions.

These reactions went on until I ended up in an episode of anaphylaxis after which point I then started having tremors, internal tremors and head pressure. 

In and out of the hospital, having repeated fainting spells (loss of consciousness), the pain went to the right side of my face and right eye, and since then I’ve been progressively losing my vision in my right eye along with being in chronic severe pain in my face and eye 24/7.

At this point I have been diagnosed with POTS. I deal with chronic severe pain in my face and eye every waking moment, as well as vertigo. I’m literally going blind and they have no idea how. It has been totally debilitating and has changed my life course. I’ve had to change my plans as a young mother as I haven’t been able to function. All I would like is to receive proper medical treatment and for no one else to suffer like I have.

Immediately after receiving my dose, I felt out of body, I ignored this and drove home. Within 24hrs I had a large mass appear protruding out of my back. That’s when I went to the hospital the first time.

They found nothing and had no answers. This was the beginning of my nightmare. After this point three days post vaccine, I started having heart problems, palpitations, chest pain, dizziness, shortness of breath. I spent countless days in the hospital and they could not explain it beyond it being a reaction to the vaccine. I was diagnosed with tachycardia and high blood pressure was noted, which I never had before. I thought I couldn’t function at this point, but it only got worse.

By July, while still dealing with the cardiac issues, I started having flares where I would flush in the face and become weak. Shortly after this I started suffering from episodes of anaphylaxis. After my last most sever episode of anaphylaxis, I started having tremors in hospital. This is when the real worst nightmare began.

After this point I started having terrible Neurological symptoms: immense head and skull pressure, pain and weakness in the right side of my face, pain and weakness in my right eye, blurry and double vision, right side limb weakness, dizziness and vertigo.

I wasn’t able to do much of anything. After more dismissal at the hospital, they sent me home. The following day I started have fainting spells and ended up fainting in my front entrance. Headed to hospital once again and had to beg for any testing. They did a CT and it was clear so they sent me home once again.

Now I have been dealing with worsening neurological symptoms for the past 2.5 months. I continue to have fainting spells, the pain and weakness, as well as pressure in my head is totally debilitating and never stops. I now have neuropathy (tingling, burning and numbness) in my face (right side), and on my right side, hand, leg and foot. I’m waiting to see a neurologist still and it’s a 12 month wait.

I’m getting to a point where I can’t work and the treatment options that have been helpful to others are expensive and out of pocket. It’s so hard as a young mom of a little toddler to try and manage it all when even taking a walk is hard.

I once lived such a full life, a life of loving the outdoors, hiking, camping and enjoying going on adventures with my family, enjoying all my time with my beautiful daughter. I have a job that I love working with special needs students. Now I live in pain everyday. I just hope and pray that I can recover. Six months of suffering and it is truly scary.

I appreciate any help or suggestions. Thank you for following my story.

November 9, 2021 UPDATE: Hi everyone, I’ve been in and out of doctors visits and they have found that I have a condition called nystagmus (didn’t have this before), where my eyes move involuntarily. This is really just another symptom of a larger issue, but I’m glad someone saw something. I also have found out I’m borderline hypoglycemic, which again wasn’t the case previously. The nystagmus can explain some of my vision issues, but not all and not the excruciating pain and discomfort I have in my face and eye 24/7. Going to keep strong and hoping to find a good naturopath to work with. I’ve been trying some acupuncture as well, but my goal is to try IV therapy and HBOT. Thanks for all your support and kindness.

October 31, 2021 UPDATE: After two better days and then two day days of severe migraines… Today is totally awful. My vertigo and dizziness is insane and feels like the life has been sucked out of me. My eye is always off sadly. Just trying to rest. Had 10hrs of sleep and still feel like I haven’t slept in a month.

You can follow her journey HERE.

Valerie Milford’s Story:

This was hard for me to open up about, but I felt it was important to do so.

Wednesday 13th Oct I got my 1st Pfizer dose. Few hours later I had heart palpitations, body aches & felt feverish, then later that night I had chest pains & was struggling to breathe so I went to the ER with my Mum. After a long wait, I was told I had PERICARDITIS – inflammation of the sac around the heart. I was sent home and advised to take Nurofen for the pain. The next few days I felt weak, tired & out of breath constantly. I was too exhausted to do anything & still had chest pains.

3 days later on Saturday, I suddenly felt my wrists & ankles feel “heavy”/weak, and my hands & feet began to ache. I was unable to walk & move my hands much due to the pain, & at times my feet would get numb. My GP prescribed me with painkillers but unfortunately it didn’t help. Seeing that my feet were worst, I was referred back to the hospital.
My feet & lower legs were cold to touch, ached at every movement, and felt like they were being pricked at when I tried to take a step. After a 6hr wait in the ER we were called in & at this point my feet & lower legs were numb from sitting for so long.

The first 2 Doctors that saw me didn’t know what was going on but told me my condition was not from Pfizer, unrelated to my nerves & blood, and that it was “all in my head” – yes these were his exact words. I didn’t feel like I was getting any help at this point. However after another Dr saw I was struggling to walk they admitted me to stay overnight to run some tests & find the cause.

3 days later my Dr & Neurologist confirmed I had NEUROPATHY in my hands and feet – a side effect from my Pfizer dose that may last 4-6 weeks.

I didn’t have any major health concerns prior, I loved being outdoors & keeping active. I got the jab so I could work, despite me being anxious about it, & now I’m unable to because of it.

Thank you all for your love & prayers during this time🤍 I’m currently recovering from home, doing check-ups with my GP every few days but still experiencing chest pains & struggling to walk due to the pain. But I know God is by my side🤍🙏🏼 

Solely doing this to create awareness🤍 

This is Chantal’s story.  Her most recent updates are at the bottom of the post.

“Your struggles develop your strength. When you go through hardships and decide not to surrender. That is strength”

This is my story…

 My name is Chantal, I’m a 37 year old Police Officer from Western Australia and I had a severe reaction after receiving the Pfizer vaccine.

To the people who threatened me with defamation charges and disciplinary action for telling my story, I am disappointed. I’m disappointed that your priority is to silence me for your own ego and agenda rather than ask if I’m ok and offer me any help! At no time have you asked if I’m ok or cared for a second about my health or welfare. You decided that putting me under more stress, when that stress can cause further risk to my life is your priority. It makes me question humanity and how any person can have such a lack of empathy towards another.

If defamation and disciplinary action is what you deem suitable than I’m not afraid. I’ve done nothing wrong, I did what you wanted and look what happened. No one has the right to take away anyone else’s experiences or tell them how they should feel. Please believe me when I say, there is nothing that you can do to me that will even compare to what I am currently experiencing. Treating someone in this way is never ok and if people can take any lesson away from this then please stand up for yourself. Set standards as to how you should be treated and don’t ever be silent if someone is treating you poorly regardless of their relationship to you.

To all the people who have told me that my experience isn’t real and that this could never be true. Before you tell anyone that they are a liar or voice your opinion, ask yourself two things. Firstly. Do I have all the information to voice my opinion and challenge the experience of another and secondly, am I qualified in voicing this opinion.

In August, my employer announced that anyone who was not vaccinated against COVID would be treated differently by having to wear masks at all times in the workplace; excluded from buildings and moved out of their positions that they have worked hard for into office type roles if they are not vaccinated. (confirmed by an industrial relations staff member). This announcement is no secret to the community as it was published on the front page of the West Australian newspaper.

Prior to this announcement, I had decided I was not getting the vaccine. I am entitled to my choice. Please note that I am not an anti-vaxer as some may call it, but I make decisions based around having sufficient information available to me which I believed and still believe I do not have. My reasons for not getting the vaccine should not be anyone else’s business but for the purposes of this post I am including it. For me, there are insufficient studies on long term health issues and the vaccine didn’t meet the usual safety checks which makes me uncomfortable. I had never had a flu vaccine in my life and I had not had a flu since 2009. I believe in good nutrition and always use nutrition to cure ailments wherever possible. I created a company based on this premise and I am very successful. I had also had a reaction to an unknown allergy and wanted to wait to speak to an immunologist prior to making a definite decision. However, this appointment was two months off. I felt as though I didn’t really have a choice. I was worried that I would be moved out of my position which is seen as a privileged role.

The morning of my appointment, I was really scared about getting the vaccine as I knew it wasn’t right for me. I spoke to the doctor about my concerns and she was willing to write me a letter to delay it but asked me what would that mean for my job. I didn’t know and it worried me. That day she had spoken to a lot of people from my job and she said that a lot of them felt threatened and put into a position to make a choice that they didn’t want to and whilst in the waiting room, my colleagues told me the same thing. The doctor told me that she was concerned about giving the vaccine to people who weren’t doing it freely by their own choice. Sadly, I joked with the doctor saying “I’ll be the one the vaccine kills.” Sadly, it could have.

Within 10 minutes of getting the Pfizer vaccine, I got vertigo and nausea and within 15 minutes I had hives all over me. The doctor and ambulance officer got the rash under control but as soon as I got home I had a fever, chills and felt very unwell. For the following 3.5 weeks I suffered rashes every day, fevers as high as 39.7, aching muscles, flu like symptoms, nausea, vomiting, diarrhea, pressure in my sinuses and a cough so bad that it felt like my blood vessels were going to explode in my face. Some days I cried because I thought I was going to die. I was so sick. When I thought I was starting to get better, I still had extreme fatigue and was constantly light headed. I went back to work but spent a lot of time laying on my office floor and struggling to get through the day.

On a Tuesday night, I noticed that my eyes felt weird. They had a heavy feeling and felt like they needed rubbing all the time. The next morning I woke up to go to work and one eye wouldn’t open and the other wouldn’t close. The one that wouldn’t close also wouldn’t blink. I thought that I had allergies so I took an antihistamine and drove one hour to work. By 9:00am, I felt my top lip go a bit funny and my work colleague told me that my face was drooping sideways and she was taking me to emergency. I will be forever grateful for her making me go as she saved my life.

Within 1 minute of being at emergency, everyone was rushing around me and I started to panic. Next second I’m getting wired up to machines and a stroke specialist and multiple other doctors and nurses were in my cubicle. I was admitted to hospital.

The next morning, I got up and had a shower but instead I ended up having a stroke. I was in the shower by myself and my body started waving uncontrollably and the right side of my body got a weird sensation. I could no longer stand and I was on the floor scared. My right side got really heavy and felt numb with a weird pins and needles type of sensation. At this stage the left side of my face was fully paralysed and I had extreme muscle weakness in my left arm and leg.

I was taken for more tests which showed that the main artery to my brain had a rupture and I had suffered a mini stroke (TIA). I was transferred to the stroke ward at a different hospital that day and from that moment on, I was monitored hourly.

I can’t tell you how scary it was being in a stroke ward with all elderly patients thinking what the hell am I doing here. I was tested for every illness and nutrient deficiency that could cause a stroke and the doctor said I was perfectly healthy and had no possible cause to what had happened to me.

While in hospital, I was monitored hourly. It was crazy. No sleep, and I was constantly scared that it would happen again. I couldn’t eat or drink properly and dribbled everything down the side of my face. It was humiliating. This was a minor issue for the doctors but for a 37 year old girl, it was a big deal. I was told that there was a 25% chance it wouldn’t heal and if it did, it would take months. This by itself was highly distressing.

I cried multiple times a day. It was mentally hard to get through every moment. I was not allowed to move at first but the nurses let me have bathroom privileges because going to the bathroom in a tray was too upsetting for me. If I moved too much or too fast I could have another stroke.

I was unable to have any treatment as the doctors deemed it too unsafe so the only thing that the doctors and I could do was wait and hope that my artery will heal itself. This will take a long time and in the mean time, my usual activities are on hold.

When I was discharged from the hospital, I was really happy as I couldn’t stand being locked up in the hospital. Don’t get me wrong, my nurses and doctors were amazing and I can’t say one thing wrong about their efforts and caring nature. However, it was so scary being home without the constant care. I wasn’t allowed to be left alone and the risk of having another stroke was and still is very high. I was in constant fear and even though my confidence is increasing, I still worry every second. I am further away from instant care and the risk of permanent brain damage is very real. I now also suffer constant nose bleeds and painful joints.

I was booked in for an appointment at the vaccine safety clinic. Sadly, there were about twenty other women the same age as me sitting around waiting. I didn’t really understand what the appointment was about until I was taken into a private room with a doctor who tried to tell me that the vaccine had nothing to do with what had happened to me but then also couldn’t tell me that it didn’t. He sat in his chair stating that it was worth the risk of having another stroke to get my second Pfizer shot. How can a doctor sit there and tell someone those things. He was willing to risk my life to meet what I believe his goal to be of getting as many people vaccinated as possible. He didn’t care about my safety and even asked after I refused the vaccine if I wanted him to call me back in three months time to see if I changed my mind. There was no respect for my decision.

The mental side of this is very hard and has required a lot of strength. I am a very active and busy person and to go from that to only being aloud to walk around the house is highly distressing. I have to be very aware of my mental health and I can’t thank my partner and friends enough for dropping everything to help and support me. I am very lucky.

I don’t want anything from telling my story accept the acknowledgement that no vaccine or medical procedure is safe for everyone. This is not my opinion, this is fact and the COVID vaccine is no exception. No one has the right to tell someone else that they have to put something in their body as they don’t know the risks to that person. It is causing a sad division in our society and not making anyone happy. If you choose to have the vaccine then great and if you don’t then that is ok too. Please be kind to each other and treat each other fairly and equally, we all deserve it. 

* Photo was me in hospital showing left side facial paralysis.

OCTOBER 29TH, 2021 UPDATE:

“I hope if I have a stroke that I recover this well. I’ve known people of similar age whose face was paralysed and never returned to normal and another who has permanent brain injuries. Chantal is out driving a car and posting on social media soon after. Looking great with the hair and make up. All power to her.” (David Geisler)

I thank you David and everyone else for your smug messages and observations and let me tell you, you are not incorrect in the vast variety of symptoms that each individual faces when having a stroke. I’m not writing this post to justify myself to you or anyone else but you have merely given me the opportunity to tell a different side of my story.

I spent some time in the stroke ward at Sir Charles Gardner hospital and every person I met and saw had different health issues as a result. The man next to me was paralysed down his right side, a man across from me had left sided facial paralysis, the lady opposite had mental confusion and her arm spasmed uncontrollably and I had left sided facial paralysis and a ruptured main artery to my brain. Every day I shared all these people’s frustration and triumphs. The crying at night when everyone had left and they thought no one could see or hear and the devastation that this brought to everyone in that ward including me was very sad.

The man next to me had so much determination. The day his physio came in and he moved slightly was a celebration for everyone in that room and let me tell you, the fact that I was determined to get my facial movement back and I could show my progress motivated the others too. 

Thank you for your note of me driving around a short time later with hair and make up done. Firstly, my partner drove because I wasn’t allowed. Second of all, any type of normality I could keep and routine in hospital kept me strong. The physical things I went through are bad but the mental side is and was so much worse. I’ve never been more scared in my life and I’ve been in some pretty hairy situations in my time. Everyday I tried to keep a routine. I had a shower then sat in my bed and put my hair up, most days in a pony tail and some days I did my make up if I was having visitors. My face was paralysed and for me, it destroyed my self esteem so doing this made me feel a little bit better.

After 5 days, I was allowed to venture outside in a wheel chair pushed by my fiance. This was the highlight of my day and did so much for my mental well being. I’m always outside doing something. I love walking and prior to getting sick I walked 50 plus kilometers a week. I loved long distance walking and competed in a 35km walk. I rode my horse, was renovating my home and loved going to the beach so being locked inside is not ideal for me.

Once I got out of hospital. It was even scarier. I thought I would be happier but I was just more worried because I didn’t have that instant medical care. I cried a lot and had panic attacks if I had any weird sensation. My fiance, being the amazing person he is, would drive me around in the car. Even if it was driving me along a road where there was a beach or took me to places where I didn’t have to move too much. He knew it would cheer me up and be good for me mentally. He was right. These things helped me. So before you start mocking or implying that my condition isn’t that serious make sure you understand the complete story. My determination and mental strength has had a huge impact on my physical progress so without me pushing through and doing all the things that you are mocking me about I wouldn’t be where I am today. I may appear normal now to everyone on the outside but the main artery to my brain is ruptured and will take a year or more to heal so on the inside I’m far from normal. The risk of having a stroke at any moment is very high and scary.

Please don’t take pleasure in thinking that I feel the need to justify these comments because I know I don’t but if I can take these comments and turn them into a lesson all I can do is thank you. Thank you for contributing to making me a stronger individual.

NOVEMBER 15th, 2021 UPDATE: 

I’ll be addressing this article over several posts. I do not wish to speak to the media as they don’t print the truth and cut and paste words to make them say what they want. If I respond. It will be on my terms every time and I will have control over what I say and what is put out there.

I have literally had enough. I am exhausted. I am exhausted mentally, physically, and emotionally. My life since 10 minutes after receiving the vaccine has been horrendous. There are no other words. I am a strong person but even this is the biggest test of my life. The physical stuff is really bad but the mental and emotional side is by far the hardest. I have to pick myself up every day. I have to find every ounce of strength I have to get through every minute.

Here is my biggest question…. why on earth am I the one that has to continue to prove that what has happened to me is real. Why is the Onus of Proof on me?

Let me first address the headline here:

“ A WA Police Officer has been accused of spreading COVID misinformation after she compared vaccine mandates as torture.”

Let’s look at who is accusing me of this. We have a medical professional who specialises in cosmetic surgery and has never met me, he does not know me and has never examined me medically in any way or read my medical notes. This is the person saying all of this and not only criticising what happened to me but comparing it to a car crash which is and will never be a side effect of having any vaccine.

“…. She compared the mandates as torture.”

This is what I said

“The thought of lining up to get the second shot and waiting to see how long it takes for my body to have a stroke, brain damage, or death is nothing short of torture.”

This is about my mindset, not anyone else. How I feel is real. I am a human being and my experience has been the scariest thing I have ever experienced so the thought of being made to have a second vaccine after everything I have experienced from just ten minutes after receiving the vaccine causes me a lot of fear and yes I would describe this as torture. I didn’t just have a stroke. I have had a lot of things happen to me and people are forgetting that. I’ve never drunk alcohol, I’ve never tried drugs or a cigarette. I drink green juices and natural powders and do my absolute best to stay fit and healthy. I was a very active person so if you look at all the circumstantial evidence and the balance of probabilities. I shouldn’t be the one constantly defending myself.

The last thing I want to address today is that I have been accused of discouraging people from getting vaccinated.

I have never encouraged nor discouraged anyone to get or not get vaccinated if they didn’t already have that opinion to start with.

My post reads

“…I don’t want anything from telling my story accept the acknowledgment that no vaccine or medical procedure is safe for everyone. This is not my opinion, this is fact and the COVID vaccine is no exception. No one has the right to tell someone else that they have to put something in their body as they don’t know the risks to that person. It is causing a sad division in our society and not making anyone happy. If you choose to have the vaccine then great and if you don’t then that is ok too. Please be kind to each other and treat each other fairly and equally, we all deserve it.

People have personally messaged me apologising because they feel as though they have to give in to getting the vaccine and they are letting me down. My response has always been the same. “You have to do what is right for you” and my response today still does not change.

I would like to address and say so much more but I need to put my health first and this is extremely stressful for me.

NOVEMBER 16th, 2021 UPDATE: 

NOVEMBER 17th, 2021 UPDATE: 

I’m telling my story because I never want to be the person who looks back & wonders what could have happened if I wasn’t too scared.

I never thought that my photos and videos would be seen by anyone else but this one shows my facial paralysis and me trying to blink during my physio exercises.

I never thought in a million years that my story would reach as many people as it did. I don’t gain any personal benefit from sharing my story. What I do risk is my job, my peace, my stress levels, being personally attacked by strangers, ridiculed, insulted and called everything under the sun.

These comments have made me cry, question my decision to tell my story and question the minds of human kind and how some people could have such a lack of compassion towards another. However, I have discovered that I have gained so many more positives than negatives. I have a sense of purpose and the resilience and mental strength I’ve gained from every single person who has come into contact with my story has been a benefit to me in some way and I hope I have done the same for all of you too.

I have only read a few negative comments on my page but I have been advised that there are many. The reason I haven’t is even though they can be hurtful, they are none of my business. I haven’t done anything personal to anyone who reads about me so their personal attack is simply to do with their own thought processes. When someone tries to destroy another person it says more about them then it does about me. My energy is more beneficial to helping myself get better than defending what happened to me so if you want to leave a negative comment then please do so but you will be wasting your time because your opinion doesn’t change the truth.

NOVEMBER 18th, 2021 UPDATE: 

NOVEMBER 19th, 2021 UPDATE: 

NOVEMBER 18th, 2021 UPDATE: 

This is Casey’s story.

This is Casey. I posted her story on Twitter on 11/1/21, but I’d like to share it again, given the severe character limitations Twitter has.

Casey now suffers from full body spasms, unbearable pain, has to use a wheelchair, and now can no longer work.

Casey, A 23-year-old warehouse worker did what her employer and government told her to do, in order to keep her job. Now she can no longer work and her prognosis is grim.

Ms. Casey Hodgkinson received her first Pfizer mRNA injection on September 25, according to her Facebook page. The adverse effects were severe and immediate. Her tongue went completely numb within an hour, followed by minor convulsions. The next day, her arms and legs went numb. Despite all that was going on, Ms. Hodgkinson tried to maintain normalcy. She went to work at Mighty Ape, an online retailer in New Zealand, on Monday, September 27. She works in the warehouse as an order picker and packer via a temp agency.

Co-workers noticed something was wrong with her. She somehow finished the day through sheer exhaustion, pain and weakness in her limbs. Ms. Hodgkinson arrived at work on Tuesday, but left early as the convulsion and weakness in her limbs worsened. She checked into the emergency room on September 29, according to Mike Wilson, who appears to have conducted an interview with Ms. Hodgkinson and her mother. Mr. Wilson made clear that he is “not anti-vax.”

Doctors admitted that Ms. Hodgkinson was having severe adverse reactions to the mRNA shots. But they also said it will “settle soon” and was a sign of “a really good immune response.” All the while, Ms. Hodgkinson was in a wheelchair because she could no longer walk on her own. By Friday, October 1, the convulsions were completely debilitating and extremely painful. Ms. Hodgkinson went to her regular doctor that day. He also exhibited completely aloofness, telling Ms. Hodgkinson that she should “try to go for a walk.”

• Since Casey first had her vaccine and visited her GP (and several hospital visits) – she has stated the following and this is still sadly taking place in her life (and much of her pain has been dismissed):
• Stabbing pain, mostly in legs (9 out of 10 and 10 out of 10 pain – some days)
• pain escalates when Casey walks.
• extreme fatigue (mental and physical)
• muscle cramps (tightness)
• numbness in limbs
• Casey’s limbs can actually lock up (SO cruel).
• Joint pain (a lot of joint pain)
• Pressure in her head (causes mind fog and a lot of pain)
• Casey has never had anything like this in her life!
• Full body spasms
• Vocal tics – which make it hard for her to speak/talk (and this is repetitive)
• Real and severe mind fog (to the point she is unable to speak or comprehend)
• Blurred vision
• Numbness in lips
• Tingling sensations in feet and hands
• Electric buzzing feeling throughout her body and it starts at the back of her head (she describes this as being in the back of her head/brain)
• She suffers agitation and restlessness – ONGOING and Casey has said this is can be for constant periods of time, something she has never faced before
• Shakes in hands and arms (and throughout the rest of her body)

 Here we are, and we exist. (Please don’t scroll passed us) away from what’s happening to us. We are people. Struggling, hurting and feeling ignored as well as dismissed.. We are feeling alienated from others when we should be getting the help we deserve. I share this to make others aware. So no one else has to go through what we are going through. Sending love and awareness. And hope for compassion.

I’m done being silent!

I’ve recently been dealing with horrible side effects of the Covid Vaccine..

I have on going muscle spams and what the Doctors are referring as Tics. I get bad episodes where my body convulses for ages.. I cant control the tics. . I also get vocal tics, and all over body tics.. and I can hardly walk now. . . I cant drive.. nor work.. which is why I got the Vaccine. So I could work!!.. and now a lot of things have been taken away.. a lot of doors maybe closed for good..

The doctors have admitted it is a bad reaction to the vaccine. And that it has more then likely made underlying issues worse. .

I’ve been dealing with it a few weeks now. With no show of it stopping.

I do not judge anyone.. let me repeat.. I do not judge “Anyones Choice”. You can be anti-Vax or stand with the Vax and I’ll still support you..

What has hurt me most of all.. is family members have treated my issue as if it is nothing.. trying to make themselves feel better. Because they believe in the Vaccine..

I dont care if you are against it or not.. all I wanted was support from family.. not issues.. I’ve had family members laugh at my ordeal. . . I’ve had family members tell others to push my mum and sisters into getting the vaccine. And family members are saying wrong information. And I am sick of it..

You have no idea what I’ve been through.. me and my mum have tried to tell you.. but you ignore it.. and I want others to know the truth. You judge me for my decision to be against the Vaccine after a horrible reaction.. I took the vaccine believing it will help.. and I was wrong. Others have reacted badly also.

When I was rushed to the hospital unable to control the tics unable to walk or communicate. (This bad episode lasted all day). I heard doctors saying how someone else had been rushed in unable to breathe because of a bad reaction to the vaccine.

You people who make people like me feel horrible.. just know that I would never do that to you.. take that how ever you will.

I do not want to change your opinion. I only Want people to know my story. And what I’ve been through.. I’ve been through a lot in my life. Dealt with heartbreak and loss. I’ve lost my dad to cancer… I’ve lost alot of people..

And if I have to loose more people. Because you judge me or treat me bad. Then it is what it is.

So this whole thing has shown me who my true family are.. and that are the ones being there for me.. and not turning a blind eye.

I leave all those who aren’t with me in my past, and hope you have healthy prosperous future..

Theres so much more to say. If you wish to know more. Message me. I will be glad to give more information. And dont worry I wont Judge!

Over all. I’ve become stronger as a person, and will continue to be. 

Sincerely

Casey

This is Casey’s story:

Casey got the vaccine on the 25th September, 2021 – 9.45am

To the best of our ability, this is the timeline of events that took place.

VACCINE DATE: Casey got the vaccine on the 25th September, 2021 – 9.45am

• Casey received Her 1st Pfizer vaccine at Greenhithe Pharmacy Unichem
• Approximately, 60 minutes later she got a numb tongue and had minor spasms
• These lasted the entire afternoon and ran into the evening
• The next day (26th Sept), Casey received numbness in her legs and arms (lasting all day)
• Her partner researched how long the side effects could last
• He was concerned at the fact his companion was shaking
• On the Monday, 27th September Casey went into work at Mighty Ape
• she was feeling exhausted all day, the same side effects taking place (people have confirmed)
• The next day on the 28th, she went into work but early on, in her shift her symptoms got worse
• Casey was losing strength in her arms and legs and it was getting harder and harder for Casey to walk
• On the 28/29th, Casey could not walk and she could not go to her job at Mighty Ape (it should be noted, that Casey works for a recruitment agency, of which Might Ape contracted).

1. FIRST TIME VISITING NORTH SHORE HOSPITAL (1 of 4 visits).

On the 29th September, Casey went from quite concerning an emergency level situation, and she was taken to the Emergency Department at North Shore Hospital.

Admitted 1937 & discharged 2147:

(7.37pm discharged 9.47pm – Casey feels she was not take her seriously and she needed a wheelchair).

The initial assessment(verbatim):

“Post covid vaccine side effects. No evidence of myo/pericarditis. Critical management/progress explained all symptoms can be attributed to the vaccine and should settle soon. Shows she’s had a really good immune response.” 

“Doesn’t preclude her from having second dose. May or may not get similar symptoms. Feeling better compared to arrival and post stemetil paracetamol and ibuprofen.”

Casey feels like she was not take seriously.

2. FIRST VISIT TO GP:

On Friday, 1st October, Casey went to her medical centre and met with a doctor. Casey was having a lot of trouble at the time and had to use a wheelchair – she had uncontrollable shakes. When she went into the doctors, her doctor told her “she should try to go for a walk” and to “try to move around”.

On the surface this might seem reasonable. Her partner has since found out, that even a small amount of mental or physical exertion sets Casey off in what is basically a shaking attack, like in the video (this does not seem to be stress related, we believe this is motor function related).

3. SECOND VISIT TO NORTH SHORE HOSPITAL (2 of 4 visits)

Casey presented to North Shore Hospital for a second time on the 4th October, 1035

She was discharged after staying 2 nights on the 6th of October at 1652 (4.52pm)

Casey was havIng trouble comprehending what was happening – throughout her stay at the hospital.

During her second hospitalisation – Casey has described herself as being “out of it” for most of the time – and claims they did not help or take her seriously.

Discharge and noes as follows (History of presenting complaint)

• “Motor and vocal tics for a few years occurring intermittently every few years” (THIS IS COMPLETELY FALSE, these only started after the vaccine)
• “Had Pfizer jab since then headaches, muscle aches and myalgias” (Muscle pains that aren’t due to underlying disease – for example, an injury)
• “report bilateral leg weakness, hard to move legs” “normal speech , eating and drinking ok, vision normal” (CASEY HAS SAID, she WAS VERY CONFUSED & SHE WAS STRUGGLING to comprehend what was going on – so these notes surprise her)
• “Over the week increasing tics, discharge from ED, recently with impression of myalgia post jab”
• “Today had worsening tics, thus presented to GP”

CLINICAL MANAGEMENT – 06/10/21

Neurological report – stated that “movements and vocalisation is consistent with tics. Exacerbation of chronic problem – “the floride and dramatic increase of tics, however also raises the possibility of super imposed functional tic disorder”

The psychiatrist review – “tics escalated due to general stress” (THIS IS COMPLETELY FALSE AND Casey denies this).

Casey is being misguided, run amuck and being told that she has “stress” and that this is a combination of mental and “underlying issues”. THIS IS SIMPLY NOT TRUE.

Further notes: “Could be conversion disorder”. (Seriously!!?)

4. THIRD VISIT TO NORTH SHORE HOSPITAL (3 of 4 visits)

• Doctor referred Casey to A neurologist- and said if it gets worse to go back to North Shore Hospital.
• Casey went to North Shore hospital, and enquired about her neurology appointment at the front desk – the kind lady informed Casey that she had an appointment, but it was not at North Shore Hospital but rather at Auckland Hospital- so she attended the appointment.

5. FIRST VISIT AUCKLAND HOSPITAL (date to be confirmed)

Casey was pretty keen to find out what was going on.

• She was unable to walk properly and had to help herself walk most of the way (until being helped to the neurology area).
• While waiting in Auckland Hospital, she started having an attack (which we believe is motor function related).
• While having this attack a group of Doctors who were walking past, paused, turned around (and what Casey is guessing as the “head doctor”) and pointed to her saying “This is what you look for!” – SPECULATION which was belitting and made Casey feel like a test subject (THIS IS REALLY UNCOOL from this particular group of doctors).
• Casey ended up being turned away and was told that she did not have an appointment – SHE WAS WAITING THERE BY HERSELF FOR 1-2 hours shaking uncontrollably- having one of her attacks & in EXTREME PAIN.

6. FOURTH VISIT TO NORTH SHORE HOSPITAL (4 of 4)

26/10/21 – Presented for her 3rd time at 2054 (10.54pm) and discharged on the 27th of October at 620AM.

Diagnosis – “History of presenting complaint” –

“Family had mentioned to staff that she possibly had tics as a child?”

(THIS IS COMPLETELY FALSE – no family member was present only Casey’s partner and he nor anyone else state or mention she had childhood tics).

CASEY HAS BEEN ROBBED OF A FAIR & ACCURATE CLINICAL ASSESSMENT!

Casey has never had tics as a child. Casey never had any sign of “TICS” prior to the vaccine.

Other note in history of presenting complaint states:

“Undiagnosed tourettes but Casey is adamant she had no symptoms until after the 29th of September” (Again, these notes are not accurate, Casey had her jab on the 25th and clearly stated she had symptoms 60 mins later).

***CASEY DID NOT HAVE UNDIAGNOSED TOURETTES!!!***

Casey was given a script for the following:

“Lorazepam” and “Risperidone”

CASEY DESERVES TREATMENT – SUPPORT, love and attention. She does not deserve to be told SHE HAS UNDERLYING TICS and other such nonsense.

This entire process has been a joke, and that fact that people on social think this is a joke, saddens and frustrates me.

Casey has been dismissed and overlooked by our health system. A HEALTH SYSTEM IN WHICH OUR MONEY PAYS FOR and she has not had support from our medical professionals.

The Medical Counsel should look into this.

– SHE WAS NOT ALLOWED A SUPPORT PERSON – her partner was TOLD TO GO HOME AT approximately 11pm (the night of her 4th visit to North Shore Hospital) and nurses told Casey’s partner – he would be allowed to be on the phone to support and help Casey understand what the doctor was saying.

Yousif Rassam (Registrar) – denied Casey the right to contact her partner – while he was present. He told Casey she was not allowed to contact her partner on the phone. This is unacceptable. Casey asked twice.

PLEASE CONTINUE READING – you are almost there…ALL EVIDENCE CAN BE PROVIDED.

POST THIS – Casey had a phone call from a GP who informed Casey, she had referred her for psychiatric help.

CASEY SPOKE WITH another GP who did not want to see Casey’s videos or meet her in person due to Covid-19. This GP referred Casey to psychiatric help and took her off the neurologist list (After her 3rd GP visit she is back on the neurologist list).

NO MEDICINE GIVEN.

CASEY URGENTLY NEEDS SOMEONE WHO ACTUALLY UNDERSTANDS THIS SITUATION.

Casey’s symptoms have been worsening – so can someone ACTUALLY please help.

This is SIMPLY unacceptable.

NEW ZEALAND CAN WE PLEASE HELP CASEY HAVE HER VOICE HEARD.

Please note – there are many people like Casey in New Zealand and around the world.

THIS IS NOT ANTI-VAX – this is about someone who has had a severe reaction to the Pfizer vaccine and no one is talking about it or taking this seriously.

7. FINAL INFORMATION:

• Since Casey first had her vaccine and visited her GP (and several hospital visits) – she has stated the following and this is still sadly taking place in her life (and much of her pain has been dismissed):
• Stabbing pain, mostly in legs (9 out of 10 and 10 out of 10 pain – some days)
• pain escalates when Casey walks.
• extreme fatigue (mental and physical)
• muscle cramps (tightness)
• numbness in limbs
• Casey’s limbs can actually lock up (SO cruel).
• Joint pain (a lot of joint pain)
• Pressure in her head (causes mind fog and a lot of pain)
• Casey has never had anything like this in her life!
• Full body spasms
• Vocal tics – which make it hard for her to speak/talk (and this is repetitive)
• Real and severe mind fog (to the point she is unable to speak or comprehend)
• Blurred vision
• Numbness in lips
• Tingling sensations in feet and hands
• Electric buzzing feeling throughout her body and it starts at the back of her head (she describes this as being in the back of her head/brain)
• She suffers agitation and restlessness – ONGOING and Casey has said this is can be for constant periods of time, something she has never faced before
• Shakes in hands and arms (and throughout the rest of her body)

This is real – just because someone is crying or in pain does not mean they are acting.

Hey everyone another update, with a new friend. Anthony Mo

We want to share our journey, and what we believe may be the right way to go.

If anyone is going through what we are or even anything strange as a result of an adverse reactions. Don’t be afraid to

reach out.

Here is the path we are now trying to go down.

We are looking to follow this for recognition and full diagnosis and cause. Keep these in mind for ways to look into your condition depending on your symptoms.

* GP – get a referral to IMAC

* Referral to a neourlgist

* Cardiologist

* Opthalmologist ( eye specialist)

* Rheumatologist

* Immunologist

The road really starts with a compassionate GP. It’s not going to be an easy journey. But people like Anthony and myself are here to find the right path. 

A recent interview with Casey is below.

This is Greg’s story:

“In the picture below, you can see the wires from my heart monitor against a background of Qld Health bed linen.

I am a fit & healthy individual with no prior medical issues and no family history of cardiac issues.

I had my first Pfizer “vaccine” in the 1st week of September 2021.

Later that day: onset of brain fog, slow to respond verbally and hard to concentrate. This continued for 3 days and then very slowly dissipated.

Then: onset of shortness of breath. I was determined to keep going with everyday life and waiting for symptoms to subside. As I said, I have always been a healthy and fit individual that has never been troubled by health issues.

The shortness of breath continued to intensify until I was unable to breath in the prone position. Therefore, I could not lay down and could not sleep without feeling like I was drowning two weeks after the pfizer injection.

I presented at 1st hospital emergency and was treated for Atrial Fibrillation (AF) with a heart rate of 170, enlarged heart and lymph nodes and fluid around heart and lungs. I was seen the next morning by a chief doctor (the one that ran that hospital) who said I was ok to have my next injection of pfizer in a few days’ time. I kept telling the doctors that this had happened after pfizer injection, but they would not listen. I wonder if this has affected the treatment and contributed to any of the permanent damage to my heart that might have been avoided. I was discharged from that hospital with prescribed medication for AF and still in and out of AF!

I attended a referral to an external (outsourced corporate medicine at every turn) echocardiogram while still in AF (!) returning an ejection fraction of 34% and I was diagnosed with heart failure. No underlying cause was found for the onset of AF or heart failure. No infection or virus etc.

2 days later, I presented at another hospital in the hope of being listened to about my adverse reaction. They didn’t listen to me either. My heart rate was 177 bpm and there was fluid around my heart and lungs. However, I was admitted, monitored and the heart medication was changed. Telemetry continued for 6 days in hospital and I started a drug called Amiodarone that can stabilise AF. But it’s pretty much poisonouswith nasty side effects the longer you take it.

Eventually, 5 days later, I had cardioversion, which is where they shock your heart with electricity to try to get sinus rhythm. It took 3 electrical shocks to my heart and it was successful for 4 hours.

After being home for 2 days, I was taken back to the hospital by ambulance as my blood pressure and heart rate were dangerously low. I had kidney and liver damage due to prescribed medication and passed blood instead of urine.Telemetry was continued in hospital and the medication prescription was adjusted and titrated. Still,no one listened to me about the pfizer injection. However, in 3 different hospital rooms in 2 separate hospitals where the rooms contained 4 people; in each room of four people, 3 of them were in hospital due to pfizer injection! The others were for AstraZeneca and all of us were being told it was not from the “vaccine”.

Telemetry continued until sinus rhythm with kidney and liver healing and then I was discharged.

The GP noted a high pulse rate? (100) and doubled my Beta Blockers.

I returned to hospital as an outpatient for a CT Angiograph that did not reveal any underlying artery or valve issues. However, my blood pressure was extremely low due to doubling the beta blockers, they said. Prescription for beta blockers halved and then halved again while still at hospital for that outpatient appointment.

My blood pressure continues to be low with heart rate in the 70s but is never stable even in sinus rhythm. It changes constantly and increases the rate or decreases the rate and I have taken to measuring the range of my heart rate as part of all my daily measuring of myself. However, sometimes my heart rate goes dangerously slow with particularly low blood pressure and my blood pressure fluctuates by up to 20 in a short space of time. I have never had a problem with blood pressure before pfizerinjection.

I attended emergency room at hospital once again last Tuesday with low blood pressure and wavering heart rate while at rest. Still, no one listened about the pfizerinjection. I was described as a “difficult historian” on my discharge letter. However, one registrar spoke to another registrar on the phone at my bedside and they decided to withhold a couple of the medications.

Since doctors no longer listen to us, I decided to continue one of the medications to improve heart function and check this with my GP and continue endless daily monitoring of my blood pressure and my heart rate and fluids.

On Saturday, I started acupuncture treatment for AF.

I am still awaiting an outpatient appointment and results of the CT Angiograph. I still have not met the Cardiologist in charge of my case.

No doctor will discuss the effects of the pfizer injection with me.

The GP says there is “no hurry for 2nd injection” but will not/cannot give me an exemption.

I am having to have regular blood tests to check liver and kidney function and for results of the side effects of Amiodarone continue.

I decided to see a private cardiologist ($300) who said that the AF and resulting heart failure was from the pfizer injection and said they were seeing a lot of this. However, he would not report it as an adverse event and would not give me an exemption for the 2nd dose. He sent me for an echocardiogram and a myocardial perfusion stress test and I will see him in 2 weeks for the results.

I am now facing a forced 2nd injection or social exclusion and no income since I won’t be allowed to work due to mandates by The Queensland Government.

I have tried to do the “right thing” and I am now left as another forgotten Australian maimed by the “vaccine” and excluded from my profession and the “vaccinated economy”.

I am telling my story in order to create more awareness about these adverse reactions and the way people who experience them are being treated.”

From Maria – the mother of a 14 year old boy in hospital

“This is an awareness post.

I feel it is my moral duty to put it out there for all to know as we are being lied to.

The risks are real, and the fears are justified.

Myocarditis is not a rare side effect of the Pfizer vaccine but an all-too-common side effect in adolescent boys.

My son is 14 years old with no underlying health issues and had his second Pfizer vaccine last Monday and became ill. He was experiencing severe headaches and on Friday morning he had pain in his chest and an irregular heartbeat. He had an ECG and a chest x-ray that came back clear but the blood test for his troponin levels were not good at all.

Troponin is a protein found in the heart muscle and a normal level is 20, whereas Troy’s level was 2,300. At this stage we don’t know the extent of damage/scarring caused to his heart. For the past four days he has been at the Monash Children’s Hospital being closely monitored, medicated and under strict bed rest. He has had an MRI and echo ultrasound of the heart. We are home now but he is still on medication and strict bed rest. He can not do anything for the next two weeks. No going for walks, no stairs, no PE, no running as physical activity can cause further damage to his heart. He is not allowed to do any sports for three months and during the 3 months gradually and painstakingly slowly build up his level of activity. This is his road to short term recovery but unfortunately as the cardiologist stated himself, they do not know what his means long term for him as the research is not there.

Everyone I spoke to at the hospital the nurses, the doctors, the cardiologist, the guy doing the MRI have all said that they are seeing a growing number of young boys presenting with the same symptoms.

Now my daughter is due for her second vaccine, but I am very apprehensive about this and am not willing to put her at risk knowing this. It does present in girls also but not as common as it is in boys.

This is not a post about not getting vaccinated, my son still stands by his convictions and decision to get vaccinated. The whole time through this ordeal he has been stoic and stayed positive in beating this. The staff at the Monash Children’s Hospital where fantastic as were Rosebud Hospital and the paramedics that took him to the Monash. As much as I am angry about his happening to my boy, we are grateful that we caught it in time. If anyone does get their boys vaccinated, please be vigilant in any symptoms they have and react straight way.

As a mother I am going through all the emotions right now, so please no judgement. We are all trying to protect our children as best we can through these unprecedented times. Was it right, wasn’t it right, I don’t know and it’s too late now, as it’s happened to my beautiful boy. Am I angry, bloody oath I am, especially as we don’t know what this means in the long term for him. It’s the unknown that will eat away at me and the fact that he is missing out on being a carefree young teenager who can’t enjoy the normal things in life like going to school, going to camp, hanging out with his friends, and going for a walk. It’s just so unfair.”

This is Fee’s Daughters Story:

“Firstly, my daughter has had every childhood vaccination with no reaction ever. Neither of us are anti vaxxers.

29/10/2021 – First dose of the Pfizer vaccine administered at 11:10 am. By 12:53 pm her left hand was freezing cold, like touching a dead body. She also told me of a pressure type feeling in the back of her head.

2:12 pm on the 29th her left hand went blue/Purple. She told me her elbow felt like it was being grabbed by someone. Gave her panadol and Nurofen as advised by vaccine clinic.

30/10/2021 – Left hand still cold but the mottling had lessened slightly. We both thought she was getting better. How wrong we were.

2/11/2021 – We attended emergency. The mottling had deepened in colour, the pain in her elbow had worsened and the pain in the back of her head had increased slightly. 5 hours in emergency. They did a round of bloods, an ultra sound of her left arm and shoulder where they found no clot. Sent home after being told they had no idea what was going on. Possibly Raynauds Disease.

3/11/2021 – Took her back to emergency that evening. The pain in her left elbow had worsened again as had the pain in her head. Her heart rate was elevated. She also began to lose mobility. I was watching my fit, healthy daughter disappear before my eyes. They admitted her at 11:00 pm that night.

4/11/2021 -She was told by the Doctor on the ward that he didn’t know what was going on but she’ll be fine in a few weeks. She was released. By this stage her right hand had begun to turn purple. She was unable to walk without assistance from me.

5/11/2021 – Take her to the GP. My daughter can no longer feed herself, dress herself, wash herself without assistance. The simplest of tasks she cannot do. Her toes and feet have turned purple. She is unable to feel the ground in her left foot. GP just sits there not sure what to say. Referral to the Neurologist with a possibility of Guillian Barre. Says that we can look at exempting her after we have seen the Neurologist.

12/11/2021 – Neurologist appointment. Nerve tests conducted. He tends to agree with the GP’s diagnosis of Guillian Barre. He admits to her hospital that day under his care. He notes there is a Neuro deficit on the left side. Speaks to her about doing a Lumbar Puncture. While we were waiting for him to type up the paperwork for hospital, I explained to her in words she could understand what Lumbar Puncture entails.

Admitted to hospital that afternoon. I was told I would have to leave even though on her previous hospital admission I was allowed in as her emotional support person. My daughter had never been admitted to hospital prior to these two occasions.

Lumbar puncture performed that afternoon. We stayed in contact via messages. Both her hands were claw like by this stage so we tried as best as we could to stay in contact.

13/11/2021 – She’s told by the Neurologist that her spinal fluid was clear and it was not Guillian Barre. He proceeded to tell her that they weren’t sure what was going on but she has Functional Neurological Disorder. Told her that he would let the Physio decide what happens next. Despite asking him again why she was turning purple and mentioning the pain in her head, he said that it didn’t warrant further investigation and that she needs to talk to her subconscious and tell it that she’s getting better.

14/11/2021 – She’s told by one of the Medical Doctors that she is not to have the nursing staff assist her in getting to the bathroom. She is to walk alone. Again my daughter asks why she is turning purple and tells this Doctor her head is beginning to hurt more when she moves. She’s ignored yet again and told it’s blood constriction but they don’t know why. They have her on panadol and Nurofen every two hours. It does nothing for the pain in her head or anywhere else.

15/11/2021 – I’m allowed in as her emotional support person. I ask the Neurologist if he could put it in writing what caused the FND. I’m met with stone cold silence and then no. Again we asked why she is turning purple and again no answer.

The Medical Doctor comes in after the Neurologist. I question the diagnosis etc and say to the Doctor that my daughter doesn’t feel like they are listening to her. I ask what in the vaccine has caused this. They don’t know. I ask why is she not allowed an exemption and what the guidelines are. They didn’t know or more to the point didn’t want to tell me. The Physio assessed her that afternoon and gave her some exercises to do.

16/11/2021 – The Neurologist sees her again. Tells her that shes 21 and doesn’t need her mother speaking for her. She asked again why she is purple and again is told it doesn’t warrant further investigation. She tells him again of the head pain, she’s completely ignored. She’s told her dizzy spells are from low iron but her iron stores weren’t that low but that’s the cause of the dizzy spells.

17/11/2021 – Shes disheartened by the lack of care shown by the Doctors. The nurses that cared for her we are most grateful for. She was released and her discharge papers clearly state the physio would follow up. We have heard nothing. There was meant to be a referral for an occupational therapist, never happened. Again no exemption and no idea if she would ever recover from this.

24/11/2021 – Telehealth appointment with the GP. By this stage she had very limited use of her right hand, mobility slightly increased but the mottling was deepening in her hands, feet and now her knees. Her exhaustion levels are beyond high. The GP asks her what she would like him to do. He had spoken to the Neurologist who had informed him that her condition wasn’t that bad. We requested a D dimer test to check for micro clotting. He told us to attend emergency for it and that was it. We said to him that we don’t agree with the diagnosis of FND. He referred us back to the same Neurologist.

Over the coming days she became exhausted quickly. She was doing the exercises the physio gave her. Still no follow up from the physio. The mottling was deepening the more she moved. The pain in her left arm, hand and her back was excruciating at times. I was lifting her into the bath and out again. The pain in the head started to increase again.

30/11/2021 Her ankles and feet swell. I take her to emergency where she tells them that the GP has told her to have the D dimer test. Shes told there’s nothing they can do and sent home 2 hours later.

3/12/2021 – I take her to a different GP. We are both extremely exhausted by this stage. I explain to the GP everything that has happened and the concern I have around the pain in the head. She lightly touches the spot where my daughter says it hurts the most and she winced in pain. The GP reluctantly orders a CT scan for her brain. I nearly cried in relief that finally someone listened. She took the time to explain the possible cause of the mottling and most importantly reassured my daughter that her symptoms are very real. The CT scan is booked for next Tuesday. We are now possibly looking at Chronic Regional Pain Syndrome.

Its been an absolute living nightmare. To see my happy, healthy daughter be reduced to shuffling, constant and often debilitating pain. Yet we were ignored. Any mention of the vaccine just swept under the carpet.

This isn’t the end of our story.

I refuse to stand by and let my daughter be dismissed for what she’s going through. The lack of any acknowledgement that the vaccine did this to her has turned from heart break to determination. And this is the vaccine they’re recommending for 5 -11 year olds? They will have a hard time convincing my younger children that this is safe.

My hope by sharing her story is awareness. Awareness that this can happen and is happening Australia wide. I also hope by sharing her story, others who have also suffered an Adverse Reaction come forward with their stories and feel less alone in their fight for any kind of medical care.

We don’t know what the future holds for her. There is every possibility she may never fully recover from this. We both hope that the Government begins to acknowledge the many who are suffering from Adverse Reactions and end the mandates that are effectively dividing the nation, friends and family.”

Miles Juneau – 31 Year Old Professional Mountain Bike Racer & Cycling Coach has been diagnosed with Pericarditis.

His story is below:

“My Heart Hurts.” Words I never thought I’d utter…Diagnosed Pericarditis.”

I respect the vaccine mandate, what I don’t understand is why they disregard the ones who suffer from it.

2 days after the 2nd dose, I experienced heart pain at the onset of exercise that left me sitting on the ground holding my chest. The optimist in me formulated rational excuses for it and went home. The next day I noticed my heart rate was constantly elevated above normal by 20 bpm during exercise. Knowing that HR can be variable, I once again wrote it off with a rational excuse. By day 3, normal deep breaths caused my heart pain and tightness. I couldn’t ignore the signs any longer.

The EKG revealed inflammation of the sac surrounding my heart. I was rushed to a cardiologist who confirmed with other tests that this nightmare was now my reality. I’ll have to wear a doctor prescribed heart rate monitor attached to my chest 24/7 for 7 days and take heart medication for the foreseeable future.

As an athlete; I’ve been stripped of my livelihood, my identity, and my passion. I know there is A LIGHT AT THE END OF THE TUNNEL one day, but that doesn’t make being in the tunnel any less miserable. I will keep my head up and continue to live by my motto, “Don’t let what you CAN’T do keep you from doing what you CAN do.”

My intentions for sharing this isn’t to cause fear or discourage the vaccine. My intentions are to hopefully encourage someone who might be feeling mild chest discomfort to please see a doctor. The earlier treatment starts, the better. This rare complication is most common in healthy males under 30 years of age and symptoms most commonly start 1-5 days after the 2nd dose.

This adverse reaction is unlikely, but if this post reaches just 1 person that may be disregarding these symptoms, that would make me happy to know my struggle helped someone else. #pericarditis

This is Cienna’s story:

I don’t even know where to begin. On Thursday October 21st at 10am I had my 2nd Pfizer shot.

That night I woke up so sick- vomiting, fever, wet in sweat, heart palpitations, headache, sore muscles & joints like hell, blurry vision. I was in so much pain at this point crying I knew something was seriously wrong I’m the first person to dust it off and never cry.

The next morning I went to the doctors who then sent me to the emergency hospital. I have been in the respiratory ward with clots all through my legs, stomach and through both lungs. The amount of clots on my lungs is equivalent to having broken ribs so a little painful & hard to breathe. As part of my treatment for my recovery I am now medicated & never have been in my life as a result of these I have internal bleeding & nose bleeds as one of the side effects of my medications along with a line of other things I choose to keep private. I had no medical issues, underlying conditions, not medicated for anything. Completely healthy. Never been sick.

Crazy to think to the left pick I was turfing with my family riding horses and the next pick is me just after my vaccination. I now have numerous doctors & specialists for a minimum of 6-12 months this is my new normal. I have also been informed to not ride my horses, my motorbikes, & train- everything I am. Drive my car and go to work. I never wanted this jab & held off for as long as I could. I got it to keep my job. If you know me personally you know how hesitant & scared I was of getting it.

Thank you everyone for the love & support. ❤️ Cienna

The past few months have been the most challenging times I’ve ever had. Within 24 hours being hospitalised and my life turned completely upside down.

When I was rushed in I was scared, but the worst part was when they told me to go say goodbye to my family. I thought that was it.

When the Dr in my ward told me that my condition was life- I’d never ride horses, motorbikes, exercise or have anything I loved back. With a long line of other things… I asked my parents to leave my room and looked out the window and thought to myself why am I still here, if this is my life I don’t want it.

My next month at home was emotional & frustrating. Trying to adjust to my new life was and still is challenging.
I’m mentally so much stronger after seeing my trauma psychologist and learning about what was happening.

As painful and challenging as it can be I refuse to sit in my bedroom all day long and let this beat me… I’m on a minimum 6 month road of recovery with 3/5 main arteries from my heart to my lungs completely blocked & fully medicated. I won’t be well or ‘normal’ for a long time but that’s okay. I will be 100% again, I’m so grateful my specialist said I will make a full recovery and I won’t stop until I am. Tough times make you stronger and I promise to come out of this a better human being in every way I possibly can be.

Thank you all for the love & support❤️❤️

I fell super unwell after Christmas Day. My health took a major decline & I ended up in hospital again. At this point in time I didn’t want to go I didn’t think I would come back knowing I only had 2 arteries open from my heart to my lungs keeping me here. The pain felt as though I was forming more clots and it was hard to breathe I also had an irregular heart beat that was racing. I did throw a tantrum to get me back into hospital. Once I was in there X-rays, blood tests, iodine scans all over again… not a single tear I’ve really learnt to just accept it will be what it will be. My blood came back in the red zone. Then the remarkable miracle happened!!! Two out of three of my blood clots have completely dissolved leaving me with only one fully blocked artery! I’m over the moon with the outcome & the Drs and nurses couldn’t believe how quickly my body got rid of the two (the estimated time was 6-12 months). On the other side… I caught COVID-19 on Christmas Day. I’m now almost out of iso and feel amazing! Only upwards from here, hoping my body will be pretty unstoppable now!!

Thank you all for your beautiful messages💖💖 and my amazing boyfriend for always being by my side and never leaving me no matter what @will_bisho

This is Jessie’s COVID Vaccination Injury:

I was against taking the COVID vaccine.

I have a neurological brain condition called intracranial hypertension.  I had approached my doctor and neurologist for a medical exemption against the vaccination but they refused.  From a consultant Neurologist at QEH, “There is no neurological reason for your to not have the COVID Vaccine.”

Because of my job & the UK government making it mandatory for NHS & healthcare workers to be vaccinated, I reluctantly had the first dose of Pfizer on January 4th, 2022.

Since having the first dose of Pfizer I have had severe headaches and severe breathing problems.  I am very breathless when I move around or walk. I also have heart palpitations.

Two days after my first Pfizer dose, I went to my local A&E department with these symptoms.

A nurse who did my initial triage said the majority of patients in A&E are vaccination injuries.

However, the doctor who I saw, said my symptoms are common and he dismissed my concerns.

An ECG of my heart was done & blood tests. I’ve not had the results back from my blood test yet but I am back home and still very unwell struggling to breathe properly.

The nurse who did the triage said the government needs to stop with the vaccinations. They’re giving it too soon and they’re giving it to too many people and it is causing many many people to become unwell from side effects.

I want to share my story to warn others of the risks.

I’m 31 years old. I took this vaccination reluctantly to keep my 13 year career in healthcare. Now it seems I’m paying the price and I have no idea how long these symptoms will last for… that’s even if I recover from them.

Thank you for helping share my story with others.

 ❤️ Jessie

This is Gabrielle and this is her story:

I’m so disappointed to be making this post.  I held out for so long, but the government pressure and mandates made each and every day harder for me.  Along with the judgement and comments from peers about how selfish I was for being vaccine free.  I received a Pfizer dose thinking my life would be easier and people would no longer discriminate against me.

About a week after receiving my first Pfizer shot, my heart started palpitating and I felt like I had run a marathon just from standing up.  I felt severe chest pains and dizziness.  I went to the A&E and my heart rate was 141BPM.  They dismissed it as anxiety.

The next day, I was rushed and wheelchaired into the hospital for heart palpitations and chest pains again.  All the while I was shaking and going in and out of consciousness.  My left arm went numb.  I saw 2 nurses and a doctor who confirmed verbally and on paper that this was because of the vaccine.

They said this is a normal and common side affect.  I’ve been off work for the past few days and barely have energy to get out of bed.  I can’t stand without feeling dizzy and puffed for more than 30 minutes at a time.  I constantly feel fatigued and in a state of confusion, zoning out frequently.  I’m 18 with heart inflammation.  That is no where near normal and should absolutely not be common.

The nurse looked at me while I was hooked up to an IV and a heart monitor and said, “don’t let this deter you from getting your other shots, you don’t want to end up in the ICU because of COVID”.  I was in an ICU because of the vaccine, and so where 2 other people in the waiting room.  The bed are being filled with vaccine injured patients.

I can’t say I didn’t know better, I did.  But the pressure became so immense and this is my biggest regret. I am one of the thousands in NZ but you won’t hear about this on the news.  They don’t care about you or your health.

Be aware of the risks of this vaccine and the boosters.  Today the governemnt has started vaccinating children.  This is not ok.

Never shame anyone for refusing this jab.  It is absolutely not selfish for refusing something that may cause irreversible damage.

❤️ – Gabrielle

This is Audrey’s story:

A perfectly healthy & active mother had her second Pfizer Vaccine in February 2021.

Three weeks later in March, she had sudden excruciating pain and complete paralysis from her belly button down.

Audrey spent six weeks in the hospital, had multiple procedures and tests that almost destroyed her, and doctors are telling her this is her new normal, that the vaccine attacked her spine and destroyed the myelin in it which is what has caused the paralysis, the the diagnosis of transverse myelitis.

After six weeks in the hospital she was sent home in a wheelchair, permanently disabled.

This is Stephanie’s story:

Stephanie had her first and only dost of the Pfizer Vaccine, on 3/1/21. 

Her arm with completely paralyzed for weeks after that first and only dose, and it caused her severe pain and agony.

Stephanie also had a giant lump where they gave her the shot, and now she suffers from neuropathy, increased pain in her bones, severe muscle weakness, severely forgetful and has brain fog, a ball in her right arm she can feel, fibromyalgia, migraines, neck pain radiating into bilateral arms, limited mobility, and her quality of life has negatively been impacted with persistent bodily pain.

Stephanie is thankful to know that she’s not alone in this journey and others are coming forward sharing their own stories too.