6 detailed Australian "vaccine" injuries
Cytotoxin creating genetic injections are not safe and effective
With thanks to Senator Gerard Rennick for standing up and posting these stories.
I will start all Australian jab injury stories with this clip.
Here is Greg Hunt, a lawyer and Australian Minister of “Health”, telling us it’s a Trial but also that it’s Safe and Effective.
The protein that is causing all the injuries below is the Spike Protein.
If you are curious about the origin of the Spike Protein and how its found its way into our bodies, here is a clip from it “maker” Peter Daszak from 2016.
If you would like to know a lot more about Peter Daszack, you can spend some time here.
To every one of these injured Australians and their families. My thoughts are with you, this should never have happened to you.
1. M (Pfizer)
“These stories need to be told for anyone that may be suffering right now.. you are not alone.
I was told by drs and politicians that the vaccines were good, they would stop you from putting strain on the medical system, stop you from having to go to emergency if you got the virus. Well I didn’t want to be responsible for putting pressure on our already strapped medical system.
I was holding out for the Novavax after doing my research. Then my work advised me that we had to have the vaccine and if we didn’t then I didn’t have a job. I wasn’t in a financial position for that to happen and have been working in my job for 11 years, so I went and rolled up my sleeve like heaps of other Australians thinking that they were doing the right thing and really let’s be honest I didn’t have a choice if I wanted to keep my job and a roof over my kids head.
Two days after my second dose of Pfz wax I started to develop chest pains I brushed it off and stayed in bed …ah that will pass.
The next day my chest felt like it was caving in, like someone was standing on it, my heart started beating the fastest I had ever felt it, I was sure I was going to have a heart attack. My husband took me to emergency.
I had blood tests, chest X-ray they gave me some medication and said it doesn’t look like you have any heart damage and after an hour the pain started to subside. I was told to go home take regular neuropen and rest it was a reaction from the vaccine and my body was trying to fight it too hard and that could take 2 weeks to two months to pass.
That was the start of the nightmare I have been living for the last nearly three weeks….
Since that first trip I have suffered ongoing heart palpitations, crushing chest pain, constant pins and needles in my hands, feet and tongue. I find it difficult to walk a few meters without my heart going crazy and my brain feeling like it doesn’t have enough oxygen. I have coughed up blood…. you think this was bad enough then the neurological symptoms started the constant tremor in my brain, feeling like I’m going to fall over when I walk, constant tinnitus in my ears, rash on both my arms and pressure that moves down to my chest and I feel like my lungs are going to collapse.
I have been carted off in two ambulances from what can only be described as seizures to be told by Drs and put on my medical notes as anxiety…. Anxiety! With no history of this condition, with NO further testing, NO referral to specialist… NO nothing….just bloody test for damage to my heart, and ECG that are apparently all good when your resting heart rate is 100+ (this is the new norm!). Told to go home, nothing they could do for me and pretty much don’t come back.
If you google COVID symptoms there is a long list of studies and articles that describe the exact symptoms I am dealing with which include neurological and nerve issues. These are not new symptoms they are currently being studied all around the world … but our trusted DRs in Victoria the state that has been dealing with this pandemic for nearly two years… They don’t seem to be able to make that connection and try to turn the blame on you…. An internal tremor in my brain is not stress, being picked up by an ambulance with a resting heart rate of 170 for 30 minutes whilst not being able to move my hands and legs, my brain and eye seizing … I won’t wear it and they shouldn’t be doing or saying that to people that were perfectly healthy prior to getting this vaccine, people that were doing exactly what they were recommending to keep them safe.
I have never felt so let down by the medical system in my life.
The answer to all this is pretty simple and it’s clear to me now.. the vaccine has made my body have the exact same immune response it would have had if I had caught the Virus itself but when you react to the vaccine you get zero diagnosis, medical treatment, intervention or sh*ts given. You’re left to fend for yourself, to go home suffer it for however long it will take for you to recover and fingers crossed you don’t just kick the bucket!
This was mandated by my employer but it’s not covered under work cover, I don’t get time to recover, my medical expenses covered, no it’s my sick leave it’s my annual leave that I’m going to be forced to take .. and at this stage god knows when I will be able to return to work again, or even when all this will go away.
My mum has been caring for me this entire time. I can hardly look after my kids, drive, do anything, all I want to do is crawl up in bed and make my head and my heart stop feeling like it’s going to burst.
I personally know so many other people that are suffering from symptoms after this amazing vaccine that gives you six months protection ….
And yes you might be the lucky ones that didn’t have any issues I’m happy for you…. but if you were in my shoes facing what I and many other people are living right now you would be looking at this from an entirely different perspective.
Our Government and our medical system are letting the rest of us down. It is negligent and they need to start telling the truth about the real number of people being affected by these vaccines and take responsibility for the fact they don’t seem to have any idea why people are reacting this way and how to fix it… but they need to say it’s real.
It has only been since taking myself to Melbourne that I’m receiving tests and referrals to specialists which if I had to wait in my small country town would be till next year. I feel it’s a little too late that the damage has been done and now my recovery will potentially be a much longer one.
The only good thing that will come out of this is that this vaccine will never touch my kids bodies… ever! I do everything I can so that they have a good immune system, they are healthy and able to fight viruses ….if they ever end up requiring medical intervention then they will hopefully get better medical treatment and care than I have ever got getting this vaccine!
Update
So this is me now sitting waiting for which appointment is it today? oh a neurologist and half and hour prior having a halter monitor put on at a cardiologist…what a push to get some medical assistance
.
It’s been three weeks since my second dose of the wax! Six hospital trips, two ambulance rides, numerous dr appointments ….for something that’s sold to us as it’s going keeping you out of hospital not put strain on the medical system …..it sure does a pretty ordinary job.. rating score !
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It’s hard to be a healthy mum running 10km one day with no heart issues no neurological symptoms to the next feeling broken and then be told but numerous drs:
- Well we just don’t have any test to figure out what it’s doing to your body! really? Wtf
- Good news is you don’t have any permanent damage! Happy days thanks guys
- It’s caused a functional disorder that should pass but we have no idea how long will take brilliant!
- We area seeing lots of people presenting with a range of symptoms after the you reckon no kidding!
I’m sorry to those that don’t want to hear about the old it hasn’t affected you, your all good. I’m sure at some stage I will recover at the expense and treatment of myself that probably won’t include any medical intervention cause it seems they haven’t worked that out yet.
If you had experienced what I have you would be screaming it from the tree tops… we need to protect our kids not from the but from being mandated. They are not worth the risk!”
2. Annette mother of Isaac (13 yo)
“Hello, my name is Annette, and I am the proud Mum to a 13-year-old boy named Isaac. Isaac just so happens to be Autistic, with a severe speech and communication disorder and ADHD.
Isaac was cleared by his paediatrician on the 27/10/2021 to have his 2nd Covid Vaccine, even after having a reaction to the 1st, Isaac had severe swelling in his legs along with aching muscles, a headache, and temperatures after the 1st vaccine but we were informed that this was a normal reaction and not to worry. Our AMAZING paediatrician did ask me not to give Isaac his medication the day of the 2nd Jab and if he had the same reaction to not give him his medication till, he was feeling better. Isaac takes Ritalin on school days only and only for the morning session.
On the 29/10/2021 at roughly 11.04am Isaac along with myself and Isaac’s older siblings, we received the 2nd Jab. I held my son’s hand and told him “Its ok my love, we can do hard things” Isaac was afraid of the needle, but he was so brave, we waited our 15 minutes and off we went to continue our day. At around 3pm I noticed Isaac was starting to get a temperature and his arm was very swollen. I gave Isaac nurofen and an Ice pack and kept a good eye on him. At 8pm Isaac was needing more nurofen, and at 9pm Panadol. I then put him to bed.
At 4.11 am on the 30/10/2021 I was calling 000. The events that led to me calling an ambulance were.
We heard a massive thump in our hallway, my husband and myself were sound asleep. I leapt out of bed to find Isaac in the hallway unable to walk, form words or understand my words, he was turning blue also. My husband and I were able to carry him to our bed and lay him down, Isaac was still unresponsive extremely pale almost grey and blue around the lips with beads of sweat all over his face. I then called 000.
Isaac started to come around and was returning to a pale colour around his lips. I checked his temperature he had a temp of 38.6, I was told to wait for the ambulance officers to arrive before giving him anything for his temp. The ambulance officers arrived very quickly and were amazing with Isaac. They checked his temp, and it was 38.6 still, they said it was safe to give him nurofen, we did that. Isaac was tachycardic, still not as responsive that they would have liked, and they advised us to let them take him to the hospital.
On the trip to the hospital the ambulance officers asked me if Isaac had ever had a febrile seizer (temperature seizer) before I said no, I did inform them that I got them as a child and I still got them as an adult.
On arrival at 5am to the hospital Isaac was so well looked after all the staff were amazing and the doctor agreed that it was most likely a febrile seizure, as they are genetic. (Isaac did not have an MRI or ECG at the hospital), in the time the nurse was monitoring him, his heart had returned to a more normal rate, his skin colour was a whiter pasty pale, and his temp was dropping. Isaac asked to go home, that he was sleepy and missed his dad.
We were able to leave at 6.46am on the 30/10/2021.
We were told not to allow Isaac to have a temp and to keep him on a well-timed nurofen and Panadol schedule for the next 48 hours.
On Tuesday the 2/11/21 Isaac was feeling much better and that was the first day he had his Ritalin to return to his normal schoolwork routine.
On the 13/11/21 Isaac fell over, directly backwards, not hitting his head and not tripping on anything, this was at about 12pm. Isaac then fell again at 2pm the same day again not tripping on anything. We decided to make an appointment with his regular GP.
On the 16/11/21 Isaac was seen by the GP, and she was concerned, she wanted bloods and an MRI done. I was driving home with Isaac after the bloods and the GP rang, she asked if I could come back as she wanted Isaac to have an ECG. The ECG showed that Isaac was having Atrial fibrillation, Isaac then needed to wear a heart monitor for 24 hours. I was also advised to stop and see the pharmacist and check on his medication as the GP can’t prescribe Ritalin and she does not have the most up to date information on it and she felt it was vital to speak to someone who works with it everyday and is educated in the medication.
I stopped and spoke to the pharmacist, the information he gave me has shaken me to the core! He said to STOP taking Ritalin immediately as it is a stimulant, it makes the heart work harder and with Isaac having Atrial fibrillation the top chambers of the heart are working harder already and the bottom chambers can’t pump the blood fast enough, so the blood clots and when the blood clots it throws clots and people DIE. YES! DIE! So, for 9 days I gave my child medication that could have killed him. Because I did not know he had a heart problem.
I take full responsibility for taking my child to get the Vaccine, I also take full responsibility for giving my son medication, it is something I must live with for the rest of my life and the guilt is crippling, I look at my son and feel like a failure of a mother because of MY actions. I am telling our story in hopes this stops it from ever happening again to another small human. Children need to be protected and if a family decides to get the vaccine for their child, they need to know that this can happen. I was not told any of this information. Isaac can never take Ritalin again and this will alter his future learning abilities and then in turn life. The small humans deserve to have their hearts monitored and the small human makers need this information to care for their child. I never ever want this to happen to another parent.
Today
Just wanted to let you know that Isaac has seen the GP and we have his full heart results back. Isaac was diagnosed with sinus arrhythmia, GP said 100% from the jab. As his Paediatrician would have noticed the problem on the 27th .
Also the hospital has lied on the paper work. They said Isaac was admitted to hospital for a viral infection. At no time did the hospital tell me this and they also said he was discharged at 10am also not true as I have the text message to my husband to pick us up at 6.46am.
Also his liver function is at 49 and should be at about 12. So the GP said that is concerning also.
He has been referred as an emergency patient to his paediatrician.”
3. Ben, an Aussie living in NZ (Pfizer)
“Firstly this isn’t a sympathy post or post of conflict. This is an awareness post. I am wanting people to know that this does happen to people that you know. If it has happened to you, then you should feel comfortable in speaking out so the health professionals are more aware.
I would like to voice that I understand everyone has individual views. I do not wish to push anyone away from their own choice, I’m am simply expressing my current diagnosis /experience from being administered my first dose of the Pfizer Vaccine.
Post injection I experienced some flu like symptoms. Headaches, cold sweats and fatigue(which are common side affects) I began getting stabbing like pain in the middle, slight left from the centre of my chest. They were dull but definitely there.
I had also lent on my left knee somehow causing a major swelling in my leg. Abnormal amount of swelling as I have never had this before.
None of this worried me till my knee started to swell quite badly and my chest pain was becoming frequent. Miki had phoned healthline and they told me to get straight to hospital. We raced straight down and had all the testing/scans carried out. Everything came up clear but was advised that my heart was possibly being irritated by the vaccine. Prescribed medication, mostly for the swelling in the knee, and headed home. Only to return if symptoms worsened.
3 days later in the afternoon I began to experience constant chest pain and shortness of breath, especially while laying down. After a few hours passed with the pain, leg still swollen and I was back down to the hospital. Another lot of tests done which came up clear and checked by a different doctor. I explained all symptoms I was suffering and I was advised my heart was suffering from Pericarditis from the vaccine. Another lot of medication and sent on my way home with this abnormally sharp chest pain.
I then saw my GP on on the 6th day who ran the tests again and saw a slight abnormality in my ECG results to confirm I was diagnosed correctly. Explaining again, if symptoms worsen or veins begin to rise in my leg to then to reach medical help.
The following morning my leg couldn’t hold my body weight and I had a varicose vein popping out from behind my knee travelling 5cm upwards and sticking out by 1cm. We immediately called the ambulance and when they arrived the vein had gone back to normal. (Unfortunately in the panic we didn’t get a photo)
Once again machines and tests carried out which were clear. The paramedics notified my local Hospital and they simply said
“If the vein is gone and his vitals are clear we don’t need to see him”
The paramedics seemed concerned and personally advised us to travel to a bigger hospital. So in the car we went for an early morning trip of 2.5hrs.
Arriving at Emergency, tests were carried out which were all clear. I then had a Dr X sit down and ask me why I was there. I explained “my chest pain and swollen leg”. She explained that she had looked over all my tests and they were clear, as I tried to explain my worsening condition with new symptoms eg; the vein in my leg and pitting edema (signs of blood clots) she cut me off saying “your tests are fine, there is nothing wrong with you, you are probably stuffing these side affects from “anxiety” and there is nothing I can do for you”
Disregarding the fact that I was told if I experienced any of these current symptoms to seek emergency help as this could possibly be a blood clot.
I had to push to ask for a D-dimer test and received a very quick ultra sound on my leg.
Due to those test coming up clear Dr X told me the clot was most likely broken down in my system, to stop all medication because my current diagnosis of “pericarditis” was incorrect and that nothing was wrong with me. I was sent home with a new diagnosis of “anxiety”. I was feeling very unsettled, without answers and confused to how I could get so many different opinions… I didn’t know who to believe.
This was the most humiliating experience to be told I was just anxious and that my symptoms were in my head.. my question at the time was if she was so certain that anxiety was the cause of these horrific symptoms.
Why didn’t she help me resolve that issue?
Im not the first person with this same experience.
Dr X then told me to leave the hospital whilst in pain.
The following day an appointment with my GP, he again confirmed my ECG results show different readings from each test which indicated acute pericarditis. he explained that reactions like these are unexplainable, happing to those who are healthy, I am unlucky and is an uncertain sort of treatment because it’s a new product they are also dealing with. An honest answer from a doctor means a hell of a lot more then being told you are suffering from anxiety because they don’t know the answers. Dr X only looked at my results at the current time and did not compare with previous ECG scans. Dr X simply didn’t want to deal with my pain because she didn’t know the answers.
After a week long ordeal of 3 hospital visits, 2 ambulance calls and a call to health-line, I was still not taken in for monitoring. Even with signs of blood clotting.
I am immensely grateful for my GP and the ambulance service who listened to me, believed me, and provided me with reassurance when all other systems failed me.
I am appalled with the New Zealand health system/gov. Restricting our lives till we get this vaccine and when we do and it goes wrong, most were unwilling to listen or help.
I did what was asked of me to protect myself and others and when it went wrong the system failed me hugely.
I am still experiencing chest pain & swelling in my knee but with medication and rest I am recovering very slowly.
I am NOT “antivax” I have personally chosen to voice my experience to be transparent with everyone as I believe this is hugely lacking, causing immense uncertainty around the vaccines.
Share my story, as anxiety isn’t the issue ”
4. Allison
“I’ve been hesitant to share this as I know how divided this has made people. I also know I may lose friends. But since hearing the news of the impending rollout for 5 to 11 year olds I felt I’m just as wrong as everyone else whose remaining silent if I don’t share my experience.
I was quite hesitant to have the V as most people know I have autoimmune issues/lupus.
I went to my GP who I’ve seeing since I was 12 & asked his advice. He said with no hesitation you must go & book in today please. If you catch you will die. I said that I was worried as In the last year I’d been having some issues that suggested brain involvement. He said it’s really safe go & have it. There is a rare chance you can get pericarditis as a side effect but we will treat it if it happens it’s easily treated.
The thought of my kids being without a mum pushed me to book in & I had my first .The first week I was fine & was encouraging family & friends to have theirs. But after 10 days I noticed I was having what felt like rapid irregular heart rate & it felt like palpitations. I brushed it off thinking I was just imagining it. After 2 days it intensified & I knew I wasn’t imaging it. I was also getting really short of breath had tingling numb feeling in my left arm & pain in my shoulder.
I went to the local ER & just walking from the car felt like my heart was bouncing out of my chest could hardly breath & felt so dizzy. They did an ECG & bloods to rule out heart attack & I was then told I was fine that I was ok to go. I Had a resting HR of 155 & I could see that my HR was quite erratic & missing beats every few beats.
Over the next few days I felt weak, exhausted & generally unwell. I was starting to have chest pain & a heavy feeling in my chest. I Was getting out of breath quite easily & had a cough, numbness tingling in my arm, pain in the shoulder, couldn’t lay down or chest pain would worsen & my HR would go crazy, I was dizzy all of the time & drinking heaps of water.
About 5 day after advice from my GP I presented to ER again as my symptoms had worsened. My GP told me to go get an MRI & cardiac ultrasound. This time it was almost like I was wrong for showing up to the ER the DR actually said why have you come back? It wasn’t until I told him that I had lupus that he said oh well we need to check you for pericarditis. But we can’t do that here you need to go through your GP get a referral for cardiac ultrasound & halter monitor.
Once again I was told my ECG was fine & bloods were fine & I was right to go home with still no treatment. When I questioned the DR about my ECG being fine when clearly I can see my HR is too high, eratic & missing a lot of beats he said well yes it is but you need to go through the proper channels & go back to your GP. It was Friday so now I had to wait until Monday.
While I was in ER a friend was in the cubicle next to me also with chest pains after having his 5 weeks earlier, was also sent home & told he was fine. Once I got home my mother called to tell me that my niece was also having similar symptoms two weeks after her & needed a heart monitor also.
I Spoke to my GP on Monday & he referred me for a cardiac ultrasound, cardiologist & halter monitor. I couldn’t get an appointment for either for 3 weeks. The thought of going through this for another 3 weeks I thought was unbelievable.
By the next Saturday the pain intensified & was having sharp stabbing pains & ache in my chest. I was out of breath felt like I had a weight in my chest & just felt really uncomfortable so I asked my husband to take me to the ER at another hospital. They took my BP then told me I’d be staying the night in ER they did Blood tests again to test for heart attack & ECG.
My HR & blood pressure still through the roof. They gave me aspirin & spray under the tongue & a potassium drip. The DR came in & asked what I thought had set this off. I said I had the then 10 days later started having these symptoms. He said the phiz? I said yes & he said I think you have pericarditis from the I thought finally I will get treatment. By this time my appointment for the cardiac ultrasound was for the next day. The DR said we will keep you here until your appointment then discharge you for the appointment & go from there. In the early hours of the morning he came in & said I will give you an anti inflammatory injection that we use in pericarditis & see if that helps. Then change of shift a new DR comes in & says your ok to go I said what about treatment? He totally brushed me off & said if it’s pericarditis it’s a mild case down playing everything.
By midmorning I could feel my heart wasn’t racing it was 75bpm, stable & I could no longer feel the ectopic beats from the anti inflammatory injection they had given me earlier. I went to the cardiac ultrasound later that day & the sonographer was lovely he said good news you don’t have myocarditis but if you don’t get a diagnosis of pericarditis from the cardiologist just know that we are seeing a lot of people with heart inflammation after the phiz.
The next day went to cardiogist who wasn’t interested in listening to any of my symptoms he said I get the gist of it you’ve had some chest pain, some missed beats , that can be normal if you drink coffee, alcohol or have a period. I said I havnt had any of those things & this is not normal. He said you stress test was fine. (I couldn’t walk on the treadmill for two minutes without almost passing out) He said you will be fine to go for your next . I said you have to be kidding I still feel as though I might die from the first. He told me that I have a leaky valve which he didn’t elaborate on.
Over the next couple of days as the anti inflammatory injection wore off the symptoms started to return. My Hr went back up, was erratic, I could feel the missed beats again & the chest pain was creeping back. I started having episodes of leg spasms that would go on for over half an hour & repeat over & over. A couple of nights it went continuously until I couldn’t walk as I couldn’t coordinate my legs.
I then began having what I think are seizures every time I would fall asleep & other disturbing neurological symptoms. Ringing in my ears & it was like the smallest sounds were amplified & agitating. I was having crazy dreams where I’d wake up & feel disoriented & confused almost like I was hallucinating. I would wake up suddenly like being jolted every time I’d fall asleep & sometimes start to seizure & so thirsty like I’ve never been before drinking a litre of water through the night. I constantly felt like I was about to seizure , my muscles constantly felt like they were vibrating. My eyes felt like they were bouncing up & down every time I’d close them to go to sleep. I had blurred vision. My head felt like it had so much pressure it felt like it was going to explode. I had sharp pains in the head constantly ( which I do get sometimes with my lupus, but these felt much more intense). I had bruising everywhere from the blood tests but not only at the puncture site, all up my arms, even on my chest where the ECG stickers where. Some days I couldn’t even walk from one room to the other I was so out of breath & I had to sit down while talking or I’d be so out of breath I felt like I might pass out.
I called my GP to tell him what had been happening & he was totally dismissive of everything I was telling him. He told me that I have anxiety & need to get treatment. So 10 days after having a vaccine with known “rare” side effect of pericarditis I have all of the symptoms of pericarditis but it’s just anxiety?
I’ve had whispers from nurses & Drs saying they aren’t allowed to comment & that Drs aren’t acknowledging reactions in fear of losing their licences & if you mention reactions in a hospital you will see how the mood changes.
I’ve since seen my Dr that I see for my autoimmune issues & he has acknowledged that I’m having an “immune reaction “ & is referring me to see a neurologist & cardiologist in the new year! That’s right still no treatment. I now know that I have a leaky heart valve, SVT & god knows what else, a whole new range of neurological symptoms & my immune system is even more buggered than it was. I’m still having symptoms & can’t do much or it flares up. It’s been 6 weeks from when I first started having these symptoms & I’m finally starting to feel like I’m improving but it’s so slow & each day is different. I know people will say yeah but you have autoimmune problems but this is happening in very healthy people as well & our medical system is failing us. All the more reason to allow exemptions for people like myself. But we are still expected to go back for a second dose even if it may kill us.
When Drs & nurses are being made to lie & are sending people home with life threatening symptoms with no treatment you have to ask why? Why is this being covered up? So think very carefully about putting this into your little ones, The thought of it chills me to the core. I am not anti vax, I am up to date with all of my other vaccinations & so are my children. But as long as I have a say they will never receive this one.
I have numerous once healthy friends who are going through identical experiences after having theirs & have all had the same experiences with ER & their Drs.”
5. Fee about her daughter (Pfizer)
“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 Im 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.”
6. Laura mum of 14 year old Samuel (Moderna)
“Time line of events
4 th of October 2021
Was 1st doze of COVID-19 Vaccination of Moderna Spikevax
- Samuel was having a sore arm and tired
For the next 3 days & a sore body Aches and pains..
9 th of November 2021
Samuel had 2 dose of Moderna
- 9/11/21 Samuel was feeling tired and sore arm
-10/11/21 sore arm and body very tired
- 13 /11/21 Samuel was saying he’s body hurting mostly lower back headache, heart pumping fast, calf’s and ankles hurting
- 22/11/21 Monday afternoon came back from school told me that he’s heart was hurting and racing while at school doing he’s work..
put him into the car and took him to our GP
They did an ECG …It didn’t show much..
GP was worried & explain that everything Samuel is explaining is an adverse reaction to the vaccine
Was giving blood work to be done ASAP..
22/11/21 Tuesday took Samuel to get blood work done
Still wasn’t feeling that good but knew he wasn’t letting me know due to being scared of the unknown…
26/11/21 Friday
Samuel couldn’t get out of bed
- took a shower
- I could see he was really struggling and I called an ambulance..
- 000 call told me there was a long wait time
- a lady called us back & asked what was happening
- I explain that Samuel was struggling and had no energy and he’s heart was hurting and all over he’s body..
- 000 told us it was normal after jab..
- then said our house was a COVID hot spot..
60 minutes + for an paramedic to arrive
Finally paramedic
Arrived check out everything on Samuel
Told us it was normal after jab for boys
Samuel age to be like this..
Told me that our home was COVID hot spot and he didn’t require ambulance .. if I was concerned to drive Samuel to the Royal Children’s Hospital ..
26/11/21 Friday
Presented to the Emergency Department of Royal Children’s Hospital Parkville Melbourne Victoria ..
12:00 pm
Triaged in at 12:38 pm
Explained Samuel’s
Symptoms heart palpitations aches and pains , headache lethargic sore body.
Waited in waiting room after being triaged in ED
Waited for a few hours in waiting room ..
Approximately 3:30 pm
Was called in to cubicle in the hospital..
Resident Doctor was dealing with us..
We explained everything that happened to Samuel..
Resident brought another lady in I believe was a nurse .
Nurse wanted to speak to Samuel on he’s own.
Samuel was reluctant for me too leave the room by
Then he was tired frustrated hurting, hungry,
Hospital staff didn’t give any information on anything.. still wasn’t sure what was happening..
Another doctor came in and check Samuel chest
We explained that Samuel has a heart murmur on he’s left side of his chest just under his nipple ..
doctor couldn’t find it .
Then I explained to please try again.. doctor then found Samuel heart murmur ..
Was told paediatric cardiologist team would come & see Samuel..
Many hours went by with very little information on anything..
New nurse came in to check on Samuel,
Was told that she is seeing this a lot & told us nothing would happen in this hospital at this moment in time..
She told me to take him home and give him 2 vitamin C & 2 vitamin D
Soak in magnesium bath for 30 minutes and should alleviate he’s symptoms until I was able too see our GP or get more medical help ..
Eventually a man came in to take an X-ray of Samuel chest
Then had nurse come back to take blood test and asked Samuel for a COVID test..
Samuel was confused why they asked him for a COVID test seeing he had been there all day in pain and in a waiting room with other sick kids..
Nurse replied that they had a right to get a COVID test from him ..
Samuel said no too the nurse then another lady came in and demanded I leave .
I asked why ?? Her reply was that they were able to ask me to leave so they could talk to Samuel on he’s own..
Samuel was extremely upset with everything happening and told the lady he had been talking to each medical person who came into the cubicle and nothing was happening or done..
Seeing the nurse by this stage was very rude and Demanded Samuel for a COVID test due too Samuel having all the symptoms ..
Samuel asked how is that possible when I have been double vaccinated with Moderna???
Then lady said why did you get jab??
When you have a heart murmur & try very hard to blame myself for bad parenting choices ..
I explain that he’s 14 years old and we spoke to our paediatrician & said it was important for him to be vaccinated & he would be protected from anything major happening to Samuel..
We agreed for the COVID test to be done..
we were told by the Nurse & the Resident doctor
That we were getting moved to short stay unit ..
Paediatric cardiologist was held up due to an unpresident day in the hospital..
By 9:30 pm our GP called
Too see how I went today with Samuel I Explained we were still at the hospital with very little information told her they did a Covid test ..
The Resident doctor came into the room again
I asked The resident doctor too please speak with our GP on the phone
I gave her my phone cause my GP was on the phone they had a Conversation about the situation Samuel was in..
After that call the Resident doctor told us she had done everything she could & Samuel was going to be discharged from ED that evening ..
I was really scared about taking Samuel home with
very little information
Was told that paediatric cardiologist couldn’t come and see him they were very busy ..
Got told they would give us discharge summary
& if anything happens over the weekend to come back in ..
I told resident doctor that I was dissatisfied with everything that happened in ED that day & if she studied too be a doctor she should know that it’s not normal for a fit and healthy Active 14 year old boy who has only asthma & heart murmur which has managed by our GP & Paediatrician .
I didn’t get anything more from our Conversation with the resident doctor
By then I was emotionally Drained and told the resident doctor that I hope she could sleep with her self at night due too
Her duty of care wasn’t met . On this occasion ..
Samuel & I left the children’s Hospital
After 10 pm that evening .
We went home and we followed instructions from our GP & the
Nurse ..
To give Samuel vitamin D 2 of them & vitamin C each morning and night with food and rest..
27/11/21 Samuel was struggling by the afternoon and I made sure that I gave him The vitamins and magnesium bath‘s ..
28/11/21 he woke up
Feeling well rested shortly after body aches and headache & chest aches..
29/11/21 took Samuel to GP she said that she had trouble getting information to do the rest of he’s tests that were required.. gave us referral
For Transthoracic Echocardiogram, Holter monitor..
my GP worked tirelessly for referrals and information for us with very little support by other professional places or they were all inundated
To see us or take care of the next steps Samuel required ..
My GP never gave up in trying to get us referrals & sending them out so we could do further tests ..
My GP didn’t receive anything from the Royal Children’s Hospital no discharge summary report ..
I left the GP & went to take a referral to one heart cardiology so we could get an appointment for echocardiogram and holter Monitor ..
In cardiology the receptionist said too leave the paperwork with her she wasn’t sure due too Samuel age if they took patients of his age ..
told me she would call me the next day (Tuesday) with information if they could do it..
I called the Royal Children’s Hospital spoke to medical records in regards to my doctor not receiving discharge summary report ..
they told me that I need to obtain copies via freedom of information ..
I was flabbergasted ..
30/11/21 decided to call the Royal Children’s Hospital again too explain everything that has happened.. the lady was happy to send me the Medical discharge ..
Via email.. I received it I forward it to my GP also..
Later on that afternoon 30/11/21 cardiology contacted me back & said they couldn’t make an appointment for Samuel due to they only see patients over 17 years of age..
I contacted my GP & she said she would continue finding a paediatric cardiologist and continue send him referrals for Samuel.. I also contacted our paediatrician
I also called
https://www.mhck.com.au/
who said they would triage accordingly due to the high demand for appointments..
We have had no luck with any call backs and my GP is having issues with Apra
I’m extremely saddened and scared for our diligent GP who diligent and has done everything she possibly can as a GP
For our family and myself
I have know her for over 20 years I have the upmost respect for her craft & has always been extremely professional GP kind intelligent knowledgeable . I’m extremely worried about my GP & no medical professional should be intimidated by authorities especially by Apra ..
Please support us all Australia’s who need medical attention and who have had adverse reactions to vaccines ..
Please support each Australian views of opinions about if it’s right for them to have a vaccine ..
Stop the mandates for this vaccine for all people in Australia & help us have our freedom of choice that our past present and future people of our land fought for us & we honour our land and our future children Health and future ..
We have all been psychologically traumatised by the last 20 months especially myself who is a survivor of domestic violence over the years and still fighting my ex who has traumatised myself and my two older children over the years..
I have fought for the last 13 years to be able to get work & support my children ..
I have been robbed of my Integrity as a parent and making informed choices in regards to the COVID-19 out break..
the media only portray one side of the story
The government has no regard for our well being of Australians .. especially when we are all now Forced and threatened with our livelihoods of no income or job..
Please listen to myself and the people of Australia ..
I didn’t bring 3 beautiful happy children into this world for coercion by our government.. or lockdowns that have been psychologically traumatic for each Australian we all have a story and I struggle to continue to smile and carry on each day.. with a lot of doors that keep closing on a majority and demographic of Australian people which has been myself at times it’s extremely difficult to get the required help ..
I sincerely appreciate your willingness to help us bless you always
Sincerely Laura and Samuel”
Thank you for helping to give these poor people a voice. The gaslighting and abhorrent treatment of these victims by the medical establishment is almost as bad as the injuries themselves. How the hell did we get here?
Ignoring these stories will not help these folks. Thank you for your articles.
https://twitter.com/DennisDDuffy/status/1482325673834430467?s=20