Hailey Bieber – 25 Year Old Hospitalized with Brain Issues With A ‘Stroke Like’ Blood Clot

March 12, 2022 in Adverse Reactions

Per an Instagram Post by Hailey Bieber, posted on 3/12/2022, she had a recent hospitalization she describes as a “small blood clot” to her brain.

“On Thursday morning, I was sitting at breakfast with my husband when I started having stroke like symptoms and was taken to the hospital. They found I had suffered a very small blood clot to my brain, which caused a small lack of oxygen, but my body had passed it on its own and I recovered completely within a few hours. Although this was definitely one of the scariest moments I’ve ever been through, I’m home now and doing well, and I’m so grateful and thankful to all the amazing doctors and nurses who took care of me! Thank you to everyone who has reached out with well wishes and concern, and for all the support and love -Hailey”

Details below from this TMZ article state Hailey Bieber’s health scare has some more details according to their sources:

Hailey Bieber was hospitalized with a brain condition that doctors think may be COVID-related … sources close to Hailey tell TMZ.

We’re told Hailey was admitted to a Palm Springs area hospital a few days ago after suffering a “medical emergency.” We’re told it affected the way she moved, and the symptoms are typical for much older people. Hailey is 25.

3/7/22 BIEBER ROCKS L.A.TMZ.com

Our sources say doctors ran a battery of tests and are looking to see if the symptoms involve COVID. As we reported, Justin came down with COVID a few weeks ago and has since recovered. As you know, Justin had to postpone his Vegas concert after coming down with the virus.

We’re told Hailey has been released from the hospital and doctors are still trying to determine what caused the issues.

Our sources say she’s now doing ok.

So was Hailey Bieber vaccinated?

Hailey and Justin did attend the Met Gala September 13, 2021.

Which according to PEOPLE: The Met Gala to Require Attendees to Be Vaccinated Against COVID-19 and Wear Masks

Hailey and Justin both attended the Met Gala, this below image came from VOGUE.

So it would seem that Hailey has been Vaccinated, just given the facts above.

I hope that she uses her platform for good and helps share the risks with others.

Others need to know that the COVID Vaccines do come with risk.

We hope Hailey makes a full recovery.

Nikki Holland – 36 Year Old Mother With Severe Adverse Reactions to Moderna COVID Vaccine

March 12, 2022 in Adverse Reactions

This is Nikki’s story:

Nikki had her 2nd Moderna vaccine 2/12/21.

Less than 36hrs after the 2nd dose, I had nausea, extreme vomiting, Gl issues and then breathing trouble.

Exactly a week post the vaccine, secondary to hypoxia from respiratory failure I was placed on the ventilator for the first time.

Nikki’s past year included:

  • 5 times on the ventilator
  • 4 life flights
  • 6 different hospitals in 2 different states
  • 1 inpatient rehab facility for a month
  • Outpatient and home health PT/OT/SLP
  • Outpatient Pulmonary Rehab
  • 2 surgeries including tracheostomy
  • Implanting suprapubic catheter
  • placement of feeding tube for a month
  • ongoing monitoring of 5 different specialists and my Primary practitioner
  • multiple tests/imaging
  • 24 medications

A year later no huge improvement and more questions than answers.

During this time I went from 3 medications to 24 medications.

From walking / jogging and working out to only able to walk short distances with a crutch and requiring wheelchair for longer distances and requiring supplemental oxygen and a tracheostomy to breathe.

Being an active mom of 3 to struggling to find enough energy to get up and do normal daily care.

From working full time as a Physical Therapist to now unable to work.

From having previous diagnoses of mild intermittent controlled asthma, Mild HTN, and occasional migraines to…. having added all the following diagnoses :

  • Respiratory Failure with hypoxia
  • Severe/moderate restrictive lung disease
  • Severe Persistent Asthma
  • Idiopathic Laryngospasms
  • Vocal Cord Dysfunction
  • Gastroparesis and needing a feeding tube at one point
  • GERD
  • GI bleed
  • Blood clots
  • Bacterial Pneumonia
  • Sepsis,
  • Unspecified Neurological Disorder
  • Neurogenic Bladder requiring Suprapubic Catheter Placement
  • Muscle Weakness
  • Ataxia
  • Hyperreflexia
  • Gait Abnormality
  • Spasms
  • Acute and Chronic Pain
  • Critical Myopathy
  • Systemic Inflammatory Response Syndrome.

I have been getting passed from doctor to doctor with no real answers just treating the symptoms with bandaids until the next big thing pops up.

Last year my medical bills added up to more than 1 million dollars billed to insurance.

Between what was not covered and billed to me, medical equipment, and lost wages this added up to thousands in bills that still continue one year later.

I’m currently trying to save up enough money obtain a better wheelchair as mine is too heavy and did not prove support I need, a portable oxygen concentrator so I don’t have to haul O2 tanks around, and pave our driveway to come closer to the house to gain easier and safer access to my home. I’ve been blessed to be able to pay monthly bills through savings and my previous work benefits, but all these medical and other expenses are becoming overwhelming.

I’ve just started a Facebook business Nikki’s Nik-Naks to attempt to sale some crafts I’ve been making to help offset these expenses but it’s not taken off yet.

A year ago I had no idea how much my life would change medically, physically, socially, emotionally, and financially… two shots, one decision to do what I thought was doing my part as a healthcare provider, was the one event that would forever change my life and set forth a cascade of medical and life events that I and my family are still having to deal with.

I just want the SAME medical support and effort to figure out what is going on in my body, AS THE SAME amount of effort, financial, and social backing that was put into the support and promotion of the one thing that caused it!

I JUST WANT TO BE HEARD.

If you have just $1 to share with Nikki, her links are below. She “did the right thing” for others and has suffered immensely because of it.

VENMO

CASH APP

This is Nikki’s story featured on Children’s Health Defense, with the video below on her story.

Kimberley Kitching – Melbourne Labor Senator Dies Suddenly at 52

March 10, 2022 in Deaths

Kimberley’s death was announced today. She died suddenly.

Her death was reported in The Guardian (article here).

She was fully vaccinated per her own twitter account.

“I feel so lucky to be fully vaccinated from corona virus as of today. Thank you to Nurse Janet for being so nice. Please go and get it done, for your health and peace of mind, for your loved ones and your country.”

“Mr Morrison says I said “we were doing well on vaccines.” Yes, we as Australians are, despite him, his late-night panicked pressers increasing vaccine hesitancy and all-round reign of error. Let’s get vaxxed and put the miserable ScoMo lockdown era behind us”

Victoria, vaccinations are now available to everyone above the age of 18.

It’s time to get vaccinated for your health, your loved ones and your community.

To quote Alanis Morissette: Isn’t it ironic? The National Disability Insurance Scheme.

Does the Australian government care about all those disabled by the COVID vaccines?

Richard Jeferson Bustamante Bautista – 8 Year Old Boy With Stevens Johnson Syndrome After Pfizer COVID Vaccine

March 10, 2022 in Adverse Reactions

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.

Deion Sanders – Pro Football Hall Of Fame Cornerback Reveals Two Toes Were Amputated Due To Blood Clots

March 9, 2022 in Adverse Reactions

Deion just revealed in his “Coach Prime” web series, that he had two toes amputated due to blood clots from what ESPN states was from a “medical setback”.

Video is below:

“They were talking about the amputation of toes,” Sanders said. “Then they were talking about the amputation of my leg from the knee down. Then, they were trying to ensure I had life.”


This clip was posted to his Instagram page (image below, video to follow):

Here is the video from his Instagram clip:


According to the TMZ video below, his toes had to be amputated because he got blood clots, due to a “prior injury” with toes that were dislocated.

In the video below, it doesn’t sound like he knows how long they’ve been dislocated, as he asks the Doctor “how long has it been like that?”, to which the Doctor replies: “probably a long time”.

“A lot is still to be determined, but he’s gonna have a procedure done a little later today,” the doctor says in the clip.

“You could lose your leg.”

Sanders still doesn’t know exactly how it happened… but has been documenting a lot of the process on social media, per a TMZ article.

A NFL article claims:

“He had a dislocated toe along with an inflamed nerve.”

“The 54-year-old Sanders underwent several surgeries. He developed a femoral arterial blood clot. He also had compartment syndrome, where his leg swelled up, and doctors had to flay open his leg to drain fluid. Sanders later had his big toe and the second toe amputated.”


Back in August 2021 Sanders revealed to the Dallas News that he’s been vaccinated for “quite a long time”, and Deion offered his thoughts on COVID Vaccines.

“One of the reasons this is very important is because first and foremost, we want to preserve life. Everybody’s talking about what they would do, what they’re not going to do, what they don’t trust, what they don’t trust,” Sanders said. “We trust a lot of things, but we need to trust the right thing.”

“One thing about this vaccination, it preserves life,” Sanders said. “I want a chance to win. I want a chance to dominate. I want a chance to take this university and these young men and women to another level. How am I going to do that if I’m not here?”


Is this a freak surgery complication or related to the #ClotShot?

You decide.

Shelby Allen – 17 Year Old Hospitalized after COVID Vaccine with Guillain-Barré Syndrome

March 9, 2022 in Adverse Reactions

Shelby Allen, a 17 year old, was hospitalized after her COVID Vaccine because she couldn’t feel her arms and legs.

“I’m on the bowling team in Dyer County and I noticed when I was throwing the ball, I couldn’t feel my arm and legs. So, I was freaking out. “

Her parents took her to the doctor in Jackson, Tennessee. Shelby is now being treated at Le Bonheur in Memphis for a rare condition known as Guillain-Barré Syndrome.

“When we got in, my doctor … told me right off the bat what she thought it was. She said ‘you have Guillain-Barré,’” Allen said.

Dr. Nick Hysmith, the medical director of infection prevention at Le Bonheur, said GBS is where “the body’s immune system gets a little bit confused and targets your nerve cells, and that leads to weakness.”

He said the adverse reaction is “extremely rare” and advised people to still get vaccinated.  😱

“I should be able to walk and get my diploma in March. I’ll be graduating high school. I should be able to walk on that stage, and I’m determined to do that. I definitely feel blessed. I could be in a lot worse situation than I am now. I could be dead, or I could be paralyzed.”

Cody Flint – 33 Year Old Pilot Severe Adverse Reaction to Pfizer COVID Vaccine

March 9, 2022 in Adverse Reactions

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 Freediver Diagnosed with Myocarditis and Pericarditis 40 days after his 2nd Pfizer Vaccine

March 9, 2022 in Adverse Reactions

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. “

Dr. Sohrab Lutchmedial – An Unexpected and Sudden Death of New Brunswick Cardiologist

March 9, 2022 in Deaths

A prominent New Brunswick cardiologist has died, suddenly and unexpectedly in his sleep, leaving behind a large gap in the system and the community.

He was 52.  “It is with profound sadness that we report the sudden and unexpected death of a colleague, friend, father, partner and inspiring spirit”, the statement from the New Brunswick Heart Centre says.

He died November 8th, 2021 in his sleep at his home in New Brunswick.

“It was sudden, unexpected for all of us. He was actually on call yesterday morning,” Légaré said in an interview.  

Images from his twitter and facebook are below.

His facebook post is below indicating his 3rd COVID Vaccine was on October 24th, 2021. 

Mike Granata – 56 Years Old Developed Multiple Organ Failure After Moderna Vaccine in August 2021

March 9, 2022 in Deaths

The following is from Mike’s obituary online.

Mike was adamant that people know what happened to him that caused his early and unexpected death.  

Message from Mike: 

“Many nurses and non-nursing staff begged me and my wife to get the truth out to the public about the Covid-19 vaccines because the truth of deaths from the vaccine was being hidden within the medical profession.”

I promised I would get the message out. 

So, here is my message: I was afraid of getting the vaccine for fear that I might die. At the insistence of my doctor, I gave in to pressure to get vaccinated. 

“On August 17th I received the Moderna vaccine and starting feeling ill three days later. I never recovered but continued to get worse. I developed multisystem inflammation and multisystem failure that medical professionals could not stop. My muscles disappeared as if to disintegrate. “

I was in ICU for several weeks and stabbed with needles up to 24 times a day for those several weeks, while also receiving 6 or 7 IVs at the same time (continuously). It was constant torture that I cannot describe. I was no longer treated as a human with feelings and a life.

I was nothing more than a covid vaccine human guinea pig and the doctors excited to participate in my fascinating progression unto death. If you want to know more, please ask my wife.  I wished I would have never gotten vaccinated. If you are not vaccinated, don’t do it unless you are ready to suffer and die.

Mike did not deserve the pain and suffering he endured.  He was a good man and deserved better.

Lisa Shaw – 44 Year Old BBC Radio Presenter Died After Brain Hemorrhage

March 9, 2022 in Deaths

An award-winning BBC radio presenter has died as a result of complications from the AstraZeneca coronavirus vaccine, a coroner has concluded.

Lisa Shaw, who worked for BBC Radio Newcastle, died at the city’s Royal Victoria Infirmary in May, a little more than three weeks after her first dose of the vaccine developed by academics at the University of Oxford.

Shaw, who was referred to by her married name, Lisa Eve, during the hearing, started complaining of headaches a few days after her vaccination. She eventually visited a hospital A&E department in Durham, where she was diagnosed with a blood clot.

She was transferred to the Royal Victoria Infirmary where she received a number of treatments, including cutting away part of her skull to relieve the pressure on her brain, but despite those efforts she died on 21 May.

Tuomo Polvikoski, a pathologist, told the coroner Shaw was fit and healthy before receiving the vaccine. Asked about the underlying cause of the fatal clotting on her brain, he said the clinical evidence “strongly supports the idea that it was, indeed, vaccine induced. Based on available clinical information, it seems to be the most likely explanation,” he said.


Shaw, who was referred to by her married name, Lisa Eve, during the hearing, started complaining of headaches a few days after her vaccination. She eventually visited a hospital A&E department in Durham, where she was diagnosed with a blood clot.

She was transferred to the Royal Victoria Infirmary where she received a number of treatments, including cutting away part of her skull to relieve the pressure on her brain, but despite those efforts she died on 21 May.

Her husband, Gareth Eve, attended the inquest with other members of the family.

Tuomo Polvikoski, a pathologist, told the coroner Shaw was fit and healthy before receiving the vaccine. Asked about the underlying cause of the fatal clotting on her brain, he said the clinical evidence “strongly supports the idea that it was, indeed, vaccine induced”.

“Based on available clinical information, it seems to be the most likely explanation,” he said.

Shaw’s death came weeks after the UK’s vaccine advisory panel restricted use of the Oxford/AstraZeneca vaccine to the over-40s, after rare reports of recipients developing unusual blood clots with low platelets. A number of other countries imposed similar restrictions or suspended use of the vaccine entirely.

The family issued a statement, which read: “This is another difficult day in what has been a devastating time for us. The death of our beloved Lisa has left a terrible void in our family and in our lives.

“She truly was the most wonderful wife, mum, daughter, sister and friend. We have said all we want to say in public at this time and ask to be left alone to grieve and rebuild our lives in private. Thank you.”

ARTICLE SOURCE

Alpa Tailor – 35 Year Old Mother of Two Died After AstraZeneca Vaccine

March 9, 2022 in Deaths

Alpa Tailor for Enfield, London, had an adverse reaction to her first dose of her AstraZeneca dose in March.

“Alpa Tailor had her first dose in March, at a time when thousands of people were dying of Covid, but fell ill a week later in a brand-new syndrome that affects just one in 50,000 people under 50. A 35-year-old “loving” mum-of-two who was otherwise healthy, died due to complications caused by the AstraZeneca coronavirus vaccine, a coroner has ruled.”

She complained of a headache, and the following day experienced paralysis on the left side of her body.

Her husband Anish said she took the vaccine to protect her family. “Life has changed for us in an unimaginable way.”

“The death of our beloved Alpa has left a huge void in our hearts and our lives, we will all truly miss her unconditional love. Alpa was a wonderful wife, loving mother, amazing daughter, sister and friend.”


On April 8th, she was rushed to the National Hospital for Neurology and Neurosurgery after showing syptoms of a stroke. 

Doctors carried out blood tests and quickly diagnosed her with a new syndrome called vaccine-induced immune thrombocytopenia and thrombosis (VITT).

Alpa had surgery that afternoon to relieve pressure on her brain and doctors initially thought she was responding well to treatment.

However by April 22, intensive care doctors noticed a change in brain function and carried out a CT scan to find massive brain hemorrhaging.

A post-mortem found Alpa had multiple brain clots.

Jonathan Hyam, the neurosurgeon at UCLH who performed Alpa’s surgery said: “This condition was a relentless wave of clots in multiple areas.

“A week or so after the surgery I was actually quite optimistic, I thought we had got her through a real nasty condition and I was really surprised when I found out about the tragic demise approximately two weeks afterwards.”

Professor Scully told the inquest: “Nobody could have considered diagnosing a brand new syndrome at this stage. It’s completely out of the blue.

“In April the number of people dying was very very few. Because of those statistics the UK has decided anyone under the age of 40 doesn’t receive an Astra Zeneca vaccination – because the risk of dying from COVID is so low compared to the risk of dying from VITT which has a significant mortality.”

Senior coroner Mary Hassell said: “Everything points in the same direction which is that Alpa had the AstraZeneca vaccination at a time when many many thousands of people in this country had died from coronavirus.

“And at the time when it was not known that there was a risk with one particular vaccine – the AstraZeneca vaccine – especially for younger patients.

“It’s very easy to look at this now and think if only she hadn’t if only a different decision had been made but she made the same decision that many millions of people in this country made.

STORY SOURCE

Jessica Berg Wilson – 37 Year Old Mother of Two Died After Johnson & Johnson Vaccine

March 9, 2022 in Deaths

A quote from Jessica’s obituary:

She had been vehemently opposed to taking the vaccine, knowing she was in good health and of a young age and thus not at risk for serious illness. In her mind, the known and unknown risks of the unproven vaccine were more of a threat. But, slowly, day by day, her freedom to choose was stripped away. Her passion to be actively involved in her children’s education—which included being a Room Mom—was, once again, blocked by government mandate. Ultimately, those who closed doors and separated mothers from their children prevailed. It cost Jessica her life. It cost her children the loving embrace of their caring mother. And it cost her husband the sacred love of his devoted wife. It cost God’s Kingdom on earth a very special soul who was just making her love felt in the hearts of so many. 

Jessica Berg Wilson, 37, of Seattle, Wash., passed away unexpectedly Sept. 7, 2021 from COVID-19 Vaccine-Induced Thrombotic Thrombocytopenia (VITT) surrounded by her loving family. Jessica was an exceptionally healthy and vibrant 37-year-old young mother with no underlying health conditions.

OBITUARY

Neil Astles – 59 Year Old Died From Blood Clots After His First AstraZeneca Dose

March 9, 2022 in Deaths

Neil Astles was a 59 year old Lawyer from Newton-Le-Willows was hospitalized with headaches and vomiting approximately two weeks after his first dose of the AstraZeneca vaccine on April 2nd, 2021.  He was diagnosed on April 3rd, 2021 with bleeding on the brain.  Mr Astles was declared dead on April 4th, 2021.

Dr McCrossen, an intensive care consultant at Liverpool’s Royal Hospital, told coroner Julie Goulding that the thrombosis and clotting that Mr. Astles suffered were a result of an adverse reaction to the vaccine.  “The headaches were from the thrombosis and pressure in the brain.”

Carole Astles, his wife, said her husband had been fit and healthy before the jab and added: “It’s just not fair.”

His cause of death was recorded as intracerebral haemorrhage, central venous sinus thrombosis and the AstraZeneca Covid-19 vaccine.

Mr Astles brother, Peter, said: “I think everybody in this country should have the vaccine. I had the vaccine even after Neil died.”

His sister, pharmacist, Dr. Alison Astles, said: “Despite what has happened to our family, we strongly believe that everyone should go for their first and second doses of the AstraZeneca vaccine. If we all have the vaccine, a few of us might have a blood clot but the evidence is that fewer people will die.”

His sister also said: “If you’ve had one dose, go ahead and have your second. If you haven’t had your dose yet make sure that you do. “Because, overall, we will save more lives by people having the vaccine than not. The risk of a clot is very, very small and my brother was extraordinarily unlucky. She said that about a week after her brother had the vaccine he began to have headaches and nausea.

STORY SOURCEHusband died after ‘extremely rare’ vaccine reaction.

Moritz Loew – Died Unexpectedly of Heart Attack

March 9, 2022 in Deaths

The sudden and unexpected death of Moritz Lowe was announced on social media on November 4th, 2021.

 Mo suffered a heart attack and passed away at home with his family. 

“Life threw us a big curve ball last night. Mo suffered a heart attack and passed away at home with his family. It was a quick Irish exit. Words fall short of the shock we are in trying to process the loss that hurts so deeply. He was magnetic, magnificent, and lived for his family and friends. He loved big. He laughed hard. He connected all of us. Due to COVID protocols we are unable to have a full service. This will not stop us from celebrating his life with all our love. We will gather together Monday Nov 8 at 4:30pm in Seattle. Details to follow. All are welcome. We will toast, weep, share stories (so so many stories), and lift him up the way he always did for us. We will share more details on ways to support Mo’s family, including gofundme and food train. Love, Mo’s team”

“There are no words. That’s how I feel and I know it’s how you feel too. All week long I have had our people with us and the first moment is always an exchange of the same sad look of knowing, of sharing in the shock and sadness at the depth of this loss, and just quiet hugging. Because there are no words. What could any of us possibly say about losing that man? Obviously the children and I are devastated and have a lot of sad times ahead. But I am taking so much comfort in seeing all of our people in our new home. Because all we ever wanted was to have a space for you all to come to laugh and play pool and chat and cry and just be you. So I am inviting – no, insisting – that if you are in Seattle now or ever will be, you must come and be in the place that was always meant for you. It’s impossible to imagine the Loew family without Mo Loew, but we’re going to need you, all of you. Please, just come. And if it helps, I can introduce you as my yoga instructor. #BigTent – Bethany”

Ashley Johns – 34 Years Old With Severe Adverse Reactions to Johnson & Johnson Vaccine

March 9, 2022 in Adverse Reactions

This is Ashley’s story:

Get The Covid-19 Vaccine They Said….

3 Months later, I’m here, 6th Floor-Cardiac Unit. But, HEY I haven’t gotten Covid!… Just a Cardiac Catheter to make sure I wasn’t dying…

Sleeping with IVs in both arms, 24 Hour Heart Monitor, Daily EKGs, Chest X-rays, 2x Daily bloodwork, Echocardiogram, Cardiac CT, Cardiac Cath Procedure, & lastly the Cardiac MRI to show the inflammation of my . Scarring indicating a heart attack, and a Coronary Artery Tear. Now I have an incision in my groin that’s super uncomfortable

They’ve figured out a decent cocktail of medications which has helped.

I’m definitely the youngest on this unit, by about 40 years and each doctor is surprised to see me here.

Telling doctors you have chest pain, palpitations and tightness is understood and they take you seriously! Especially when your Troponin Levels reach 7.30!!  (0.4 – 0.39)

Update: After reviewing the Cardiac MRI, it show’s the inflammation & also shows signs of recent scarring (heart attack) and a coronary artery tear!! So they just started me on this new med: “Isosorbide Dinitrate” my Cardiologist seems to think that with the right combination of meds and rest, that this “coronary artery tear” should heal on its own-eventually? 6-8 months?

Update: I made it home finally!! I’m doing okay. Long Road to Recovery. I still feel weird. I can’t lift over 10lbs, on 6 different new medications. Still have random weird heart palpitations throughout the day/night. But so far I’m alright. Cardiologist says it may take 6-8 months for this coronary artery tear to heal. However the Myocarditis can come back any day/month/year unexpectedly . I left the hospital with a torn heart, and a New morning routine of meds that mirrors my Grammie’s. . 34 and on Heart & Blood Pressure Medication’s & Plavix. Ect. Unbelievable. But to hold my baby again!! That may have already healed my heart I’ve never seen a little boys eyes light up more in my life then to hold his mommy again! I was instructed by 2 Cardiologist’s and an Infectious Disease Dr. to NEVER receive another COVID Vaccine again!! #ThanksCovidVaccine #GoodGame

Ashely Johns, a healthy 34 Year Old mother in Michigan is now suffering from severe adverse reactions to the Johnson and Johnson COVID vaccine.

Ashley has suffered from an apparent heart attack, myopericardidits, weeks of hospitalizations, and months of testing and a laundry list of medications.

Her doctors have conclude her conditions are most likely to have been caused by her Johnson & Johnson vaccine.

 My case is probably 1 in a million, but it happened to me, so I’m not going to support the J&J vaccine, because I’m having these complications and life changes.  I have had a few people reach out to me and I just suggested that they not get the J&J shot. Now I just have to live with whatever, until I finish this medication, and pray it doesn’t come back again. I was instructed by 2 Cardiologist’s and an Infectious Disease Dr. to NEVER receive another COVID Vaccine again! 

Leah Edgar – Severe Adverse Reactions from Pfizer Covid Vaccine

March 9, 2022 in Adverse Reactions

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.

Amanda Johnson – 31 Years Old With Vaccine Induced Multiple Sclerosis

March 9, 2022 in Adverse Reactions

This is Amanda’s story.

 My name is Amanda Johnson. I am 31 years old from Oklahoma.

In late March, I recieved my first  and only dose of Moderna. 

Within half an hour of vaccination, my skin started turning red on my injection arm. It was very sunburn like and followed by a blistering rash with hard nodules, a stiff neck, the worst headache and eye pain of my life, tachycardia, dizziness, nausea, and fever.

I was put on prednisone to help the rash but my symptoms never improved. They progressed until one morning, I couldnt feel my leg. It wasnt until I could no longer tell when I had to urinate that a brain MRI was ordered. It was abnormal and suggestive of demyelinating disease. Because of this, a lumbar puncture was ordered, which also turned out to be abnormal. 

I was diagnosed with first onset Multiple Sclerosis- Remitting Relapsing MS. 

Only after a serious diagnosis was made did they look further into my months long tachycardia issue. I had an abnormal EKG which promoted and echocardiogram and an event monitor which I am still currently wearing. 

I was not the healthiest person prior to vaccination, although my underlying autoimmune issues were well maintained and controlled. According to the National Institutes of Health, there are only 17 reported cases of my pre-existing condition and MS occuring together. That would make me one in nearly half a BILLION, and the only thing that changed was the vaccination I recieved.  The National Institutes of Health has now found a correlation between first onset Multiple Sclerosis and the covid-19 vaccine. 

Calling us a rare statistic or blaming our illness on pre existing issues is not only disheartening, its also dismissive- Dismissive of our pain, dismissive of our suffering, dismissive of our experiences.

Had my doctor not looked further into my case and held onto the immune theory, my brain could have incurred much more damage. I am thankful he thought outside of the box eventually and looked further into the neurological spectrum of things. Having a pre existing condition shouldnt discredit someones illness and reaction to vaccination, especially autoimmune problems. Having an autoimmune issue shouldnt disposition us to be the chosen martyrs to society for vaccine reactions. 

I digress to say, I used to love fishing, fossil hunting, and mycology/entomology studies. You could regularly find me at the local rivers or lakes with my children enjoying life. Now I cant stand for long periods of time wothout my heart rate being explosive, or losing my balance, or tripping over my feet from not being able to feel them.

I believed the lie that this vaccine was totally safe and effective. I believed the lie that this vaccine would create immunity. In doing so, I unknowingly sacrificed the best parts of my life. I am now permanently disabled. Prior to popular opinion, I dont feel it was for the greater good. Its not only me who deals with the consequences of my unfortunate demise- its also my children and family. 

Amanda thought her VAERS report had be filed previously, but recently found out it had not been.  It was recently filed for her, and will be viewable on the CDC website in a few weeks.  Amanda’s VAERS report will be published here once available.  

Amanda has been banned from Facebook and Instagram for sharing what has happened to her as a result of her one and only Moderna COVID Vaccine and the adverse reaction it caused her.

Amanda’s VAERS report is below.

Valerie Milford – 20 Year Old With Severe Adverse Reactions After 1st Dose of Pfizer COVID Vaccine

March 9, 2022 in Adverse Reactions

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🤍 

Ernesto Ramirez – 16 Year Old Suddenly Died 5 Days After First Pfizer COVID Vaccine

March 8, 2022 in Deaths

This is Ernesto’s story:

My name is Ernest Ramirez, I was a single parent who lost my son a few days after he received the Pfizer shot.

Ernesto, my son, received the vaccine and, following his death, the only explanation that was given to me was an enlarged heart.

My son was in good health, and regularly played baseball since he was 7 years old.

Advertising claimed that the vaccine is safe for adolescents, and this convinced me to book-in Ernesto Jr. for the jab on April 19th.

Five days later he died.

I need to spread my story so that hopefully no one else will go through what I’m going through.

Ernesto Jr was my world and I feel I need to fight for him and others that are also suffering.

It kills me to come home to an empty house.

We need to yell, we need to fight, we need to do something. His life was worth much more than what the Government or anybody else thinks. 

I love the hell out of my country but I do not trust my Government anymore. 

Ernesto died of an enlarged heart five days after the jab, according to his autopsy which showed his heart was double the normal size.

Please follow Ernesto Ramirez Sr’s journey for justice and truth HERE.

Chantal Uren – 37 Years Old With Severe Adverse Reactions to Pfizer Vaccine

March 8, 2022 in Adverse Reactions

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: 

Rory Nairn – Healthy 26 Year Old Went Into Cardiac Arrest and Died

March 8, 2022 in Deaths

This is Rory’s story:

I’d like to share Rory’s story.

As many of you may know my fiancé Rory passed away on the morning of 17 November.

I believe my partner was a victim of adverse cardiac reaction caused by the Vaccine.

Rory regretfully had his first Vaccine on the morning of the 5th of November. He started feeling heart flutters that evening, we put this down to stress as we were in the process of selling and buying a house and planning a wedding.

We never, ever considered the events that followed.

Rory had heart palpitations regularly at night, and again, we thought this was stress. 12 days later, Rory was up and down again during the night with his heart palpitations and an ‘uncomfortable’ feeling in his chest. We finally decided to head to hospital at 3am for reassurance.

Within moments, Rory went into cardiac arrest and died instantly in our home.

After 40 minutes of attempts/ CPR from the paramedics, he was pronounced dead.

He was 26 years old, with no pre-existing medical conditions. He played rugby, went diving and hunting on the weekends, worked hard as a plumber, and had his whole life ahead of him.

We had our whole life’s ahead of us!

Initial Autopsy report: unknown cause of death.

Further report focused on heart problems will take an extended amount of time to receive final conclusion.

I initially stated that Rory had chest pains prior to the Vaccine and commented this on posts. This was in hopes of getting insensitive posts regarding his death removed, while we went through a time of utmost hell and grief.

The media attention we received was overwhelming and unwelcome.

– Why are young and fit people experiencing heart issues?

– Why are Vaccine related deaths not reported on our 1pm updates or any media releases?

– Why is the government protecting the elderly from c19, but not protecting healthy young men from this Vaccine.

If we had known about these issues, maybe we would have thought twice about this, and Rory would still be with us.

For our families, this is about informed consent.

Why are we not told about these side effects and what to do if we experience them?

We need to talk about this.

Ever since Rory passed, I have had multiple people contacting me with their stories of their experiences (mostly cardiovascular related). Personally I have had both shots and was previously pro-Vaccine, so have been on both sides of the fence blindly following misinformation.

I urge anyone who experiences any heart symptoms post Vaccine to seek medical advice at a hospital immediately.

Please share this post to spread awareness about heart related side effects due to the Vaccine.

26 year olds should not be going into cardiac arrest.

Please keep comments sensitive to our families, I am not here to debate the pros and cons of the Vaccine and will not be replying to any argumentative comments.

This is Rory’s story

Holly Angel – 28 Years Old With Severe Adverse Reactions to the Moderna COVID Vaccine

March 8, 2022 in Adverse Reactions

This is Holly’s story to her adverse reactions to the Moderna COVID Vaccine:

Moderna, shot number one back on the 12th of February. I was thrilled. I called everyone I knew because they were tossing out extras! I was proud to be vaccinated for my family and community. I am not anti-vax. I still want to believe and hope that this vaccine does some good for our world, but I slowly lose hope as I slowly lose my life and am left without answers and without any direction to recover.

I need help. Share my story.

After my first shot, I felt normal. I got in the car and said, “I have a weird metallic taste in my mouth. Like static or electric or blood?” This taste lasted a few hours and went away. I really wasn’t sore, I didn’t have a fever – I felt normal! I totally expected to have some sort of rough feeling, but I was okay. On February 20th, eight days later I woke up at my new boyfriends house with numbness, tingling, and a horribly embarrassing twitching in my face. I felt “funny”. I apologized for my facial twitches that I couldn’t control and they were pretty severe. The numbness crept into my hands and at the point I decided I needed to return home. On my drive home the numbness began moving down my legs and they started to feel heavy. I should have probably pulled over, but I pushed myself to focus to make it home. By the time I got home I could barely walk because I couldn’t feel my legs. Horrible cramping and spasms were in both of my legs and became painful. By that evening I could not walk, I was paralyzed from the waist down, hands numb, face twitching. I thought I was having a reaction to a medication I had been on for years that could numbness so I called my prescribing doctor – they didn’t think this was a reaction due to no changes in dosage or any other medications. The only new thing in my life was the recent vaccine so I mentioned this to my doctor thinking it had interacted with my medication, but again they were not on board with my ideas. The doctor recommended to monitor my symptoms and to go to the hospital if things worsened.

Overnight, my symptoms remained the same. I woke up on Sunday, February 21st, 2021 and I still could not walk, I could not feel my legs. My legs were still twitching and cramping. My face was still numb and tingling, but the twitching had stopped in the face. My hands had stopped tingling. At this point my mother who is a nurse suggested that I call Moderna, the vaccine provider, to report a possible side effect of the vaccine. Upon contacting Moderna, the company thought that it could possibly be a reaction between the Topamax medication and the vaccine, but they had no current information about these two having any interactions. They thanked me for reporting and told me to go to an emergency room if my symptoms continued or worsen.

Throughout the day on Sunday, February 21st, my symptoms remained. I was able to get to my feet, but I walking like a newborn baby giraffe or as my mother described, like a 105 year old woman. I was unable to feel my legs completely, lift them, move them without lifting them with physical help of my arms moving them. At this point on Sunday night I decided to contact my Primary Care Physician at UC Health. She noted that this sounded similar to Guillain-Barre and that I sound immediately go to an Emergency Department before the symptoms get any worse. It was late on a Sunday night and I was unable to drive myself, so I waited.

Overnight on Sunday into Monday I began experiencing light flashes in my eyes, heart races, lower back pain, and worsening cramping in my legs. I knew that I needed to seek treatment in an emergency room.

On Monday, February 22nd, 2021 I was taken to the University of Cincinnati Hospital’s Emergency Room Department. They conducted blood work and a physical examination, but did not want to proceed with any MRI’s or CAT scans. The ER the doctors were baffled. They could not figure out what was causing my paralysis other than the vaccine was the only new thing that had been introduced to my body, but they could not verify or diagnose anything. They let me go with a referral to neurology.

While we were sitting in the ER my cousin, a nurse anesthetist at another local hospital, called my mother who was with me with some very alarming news. Her co-worker, had experienced the same symptoms back in December and was just going through recovery after his first dose of the COVID-19 vaccine. He was told by the CDC there had been 19 reported cases through the CDC where after the first dose of the vaccine people have reported numbness, tingling, and the lose of the ability to walk after receiving the first dose of the mRNA vaccine, both Moderna and Pfizer. Her co-worker was also in the same age range as myself, very healthy, young, active. He was officially diagnosed with Transverse Myletis. He has taken a full two months to regain the ability to walk and still has numb patches on his legs. He walks very slowly, but is walking. He returned to work, but cannot return to his normal life working out and being active because he does not have the strength. He was told not to get the second dose of the vaccine.

There are unreported cases in this area by physicians who do not know where to turn with this information. It is hard to link these symptoms and cases because they are so obscure, but these same symptoms are occurring with those who have also had COVID-19. When I was being seen for an EMG test of my legs the physician performing the test said to us, “I have a patient who received the vaccine and has the symptoms, maybe I should report it!”. My Grandmother’s physician at that time sent a patient of hers with the same symptoms to neurology. I think this uncommon side effect is more common than is being reported and no one knows where to turn with the information.

I finally got into the head of Neurology at UC. I was told, “it’ll probably get better”, basically saying that they don’t know what they can do and they are at a loss for knowing what this is and why this is happening to people after the first dose of the mRNA vaccine. Doctors don’t have answers and the vaccine companies aren’t offering information to help link these side effects together. The physician told me not to proceed with the second dose of the vaccine due to neurological side effect that I have had. I should benefit from the first dose and it is not safe for me to get the second dose from this side effect.

I was unable to walk for weeks since the reaction began on Feb. 20th. I wasn’t been able to drive or live my normal life. I couldn’t use stairs, walk long distances, stand for very long periods of time. I was twenty-eight years old and I walked like an eighty year old woman, wobbly.

I recovered from the paralysis just as the doctors said after two months of wobbling around. I regained my strength with all of my will and determination. Unknown reasons for my paralysis that are still left a mystery today and have no cause, other than possible vaccine reaction. The only symptom from that specific incident that remained was facial twitching, it never went away.

I thought facial twitching was my only lasting effect. First, all of my other symptoms didn’t seem related. Nose bleeds, easy bruising, itching, cuts that never healed, hair loss, shortness of breath, extremely foamy and smelly urine, fatigue, and weight loss. I looked into the mirror in July of this year and said, “I think I am dying.” I thought this several times to myself as my nose bled and felt “off”. I caught staph infection on my face and on my body from a simple cut, I was covered in bruising from people just holding my arms. I felt sick, but being the strong woman I am, I pushed on and smiled through it – thinking this would pass. I had been diagnosed with Lupus over ten years ago and it went basically into remission with my determination and dietary habits. I had felt fine. I thought what I was experiencing at that moment was maybe a new Lupus flare up so I called my doctor to check out my really strange situation, expecting that after this many years it was just time for Lupus to come back again. She tested me for a handful of things, my proteinuria and creatine levels were rising. Most everything else was normal in July so she referred me to Nephrology and Rheumatology. I couldn’t get in to either specialist until November. I waited, but demanding a sooner appointment fearing something was going on – they didn’t have any openings. My body felt worse the longer time went on. Flank pain, weakness, extreme weight loss just to name a few symptoms. I went from a size 6 to a size 00.

This brings us to current times. I am very sick. My proteinuria and creatine levels are extraordinarily high. My Kappa levels are elevated. I had an emergency kidney biopsy that shows damages related to kidney disease, but not related to Lupus and not related to any other disease because none of the other tests thus far align with a cause. The damage to my Kidneys aren’t going to require transplant currently or something that cannot be managed, but if the damage doesn’t stop I will continue to ruin my kidneys with 3000mg of protein running through them with the changes happening inside of them as it is. Yes, extraordinarily high levels with no known cause and various other random tests that are off. Many of my test results show a number of varied abnormalities that have stunned and baffled the doctors. Again, they are at almost a loss for a reason for why I’m sick, why I’m malnourished, why I’m nearly dead and I feel absolutely miserable. Now, when I eat I am in pain, I am sick, my kidneys burn. I have been eating a very curated kidney disease friendly diet from the most organic, plant based items. It helps some, but my body still finds many of the items upsetting and painful. The doctors have ordered a Rare Disease Genetics Disorders Test because again I have been tested for almost every known disease – we are having to test for the rarest to link all of my abnormal test results together to find relief and answers.

The only thing that has changed in my entire life is the Moderna vaccine. I was healthy, happy, normal prior to February and have been in a rapid, yet slow decline since that day. After hearing Kyle Warner, a famous healthy mountain biker, speak about his experience with the vaccine injury and listening to the three hour testimonies at Congress I can only help but believe that all that I am experiencing is a vaccine reaction. His first symptom was a metallic taste in his mouth. This is where I began.

We need answers. We need support. I do not want to feel like this anymore. I want my life back. I want to feel better and I don’t want to fear rare diseases and dying. I have had to worry about incurable diseases like Myeloma, Renal Failure, and now I’m going to the rare diseases. Some of these things aren’t off the table and I am still going through testing to truly rule out these terrifying life threatening diseases. The effects of the things that are happening are causing permanent damages to my body. I may have recovered from the paralysis, but I have facial twitching and I cannot reverse renal damage. I want this to end before it ends me. We need help. I am not alone.

This is my story.

I now believe I was injured by Moderna.

I am not anti-vaccine, but pro-support for those who need answers.

Everything has side effects, even cheese – we need to know the risks and how to react when they happen.

I deserve to be okay, we all do.

Casey Hodgkinson – 23 Years Old With Severe Adverse Reaction to 1st Pfizer Dose

March 8, 2022 in Adverse Reactions

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.

Justine Luzzi – Severe Adverse Reactions to Moderna COVID Vaccine

March 8, 2022 in Adverse Reactions

This is Justine’s story:

SEPTEMBER 5TH, 2021 UPDATE:

Today marks 3 months since I’ve been sick from my vaccine injury.

Some updates:

Right now the adverse side effects that are lingering are chronic headache, tightness in my head, some light confusion, and sometimes difficulty critically thinking. My eyesight has improved dramatically. The dizziness and vertigo seems to have subsided. And no chest or jaw pains for weeks.

I am so grateful my body is healing. This is the last week of my ozone sauna therapy treatments. That would make 7 total. That’s around the recommended amount for my situation, but if I intuitively feel like I need more sessions, I’ll do them. It’s also the last week of my PEMF therapy, but will continue the treatments at home by buying a PEMF mat. I also did a one-off lymphatic drainage massage yesterday and I felt pretty good after!

I finally feel I have the right combination of supplements, herbs, and vitamins. However, I was able to get an appointment for the best herbalist in NYC on Tuesday, AND my insurance covers it, so I’m going to see if maybe I’m missing something. Maybe there’s a homeopathic elixir that can be added.

I heard through the grapevine that there is a functional medicine doctor in NYC treating people for neurological complications from the jab. I called for an appointment and he is booked until October 27th. I was able to get on a waitlist fo cancellations, but this guy must be good, and it’s worth the wait. He will also be able to help me interpret my genetics test, which by the way, the cheek swab has not come in the mail quite yet, but should be here soon. I’m excited to see if I have the MTHFR gene mutation, which would explain A LOT.

Something new I’m trying, as in the last few days, is intermittent fasting and getting my body into ketosis. Apparently this is a good way to detox and cleanse the body, reduce inflammation, and rejuvenate the cells. I am currently doing 14 hours, but working my way up to 16. I’m eating virtually no carbs, just lots of vegetables, eggs, nuts, and fatty fish. Whether I need a long-term fast, that I’m unsure of, and will ask my doctor. I have seen and heard miraculous stories of healing from long term fasting.

And that’s it!! It’s a waiting game at this point. I’m still open to different suggestions, but I can almost guarantee I tried them already. I feel like I have tried everything at least once. I am currently eyeing stem cell patches, but need to do more research.

Thank you as usual for the continued support and prayers. I can’t wait for the day my posts get to regularly scheduled programming!

AUGUST 19TH, 2021 UPDATE:

Update on my vaccine injury recovery process:

Hey everyone! Just want to say thank you to everyone checking in on me! Everyone has been so kind and graceful as I slowly heal and get this thing under control.

There’s been a few updates:

As far as WHAT the vaccine injury is- looks like my body is just not reacting properly to the spike proteins and mRNA. My PCP thought it could be two other things; a heavy metal leak from the v@cclne (which happens rarely, but does happen) OR the v@cclne triggered an autoimmune disease (which he admitted he’s been seeing a lot). I was tested for both heavy metals and inflammation, in which they came back negative. So he said there’s only one explanation left; the spike proteins and mRNA.

Usually in spirituality (which is my wheelhouse) you ask yourself the question ‘Why is this happening FOR me?” instead of “Why me?” This question is super helpful in figuring out why you’re experiencing what you’re experiencing and to view the bigger picture of life lessons, karma, purpose, and information regarding your soul contract. This question is helpful for health related issues, but the better question for this is “WHY ME?”

Turns out, it’s quite possible I have the MTHFR gene mutation. This gene mutation has been linked to vaccine injuries for DECADES. Yet, for some reason, it’s not public knowledge. I ordered a genetics test, but that will take weeks to get results.

The PCP recommended I work with alternative medicine practitioners, so I’m officially done with Western medicine. They can’t help me. They’ve said it time and time again.

After much research, I decided to try two alternative medicine therapies. One is called Ozone sauna therapy. This is where you step into a sauna and they release ozone gas (smells rancid by the way!) and basically it works with your body on a cellular level. People use this therapy for all types of issues, including chemotherapy recovery, major sports injuries, and anti-aging practices in general. The second healing modality I tried was PEMF, which is like an electromagnetic pulse therapy. You get muscle tested for the root of the issue and then they set the machine to that frequency of healing. Both modalities made me feel GREAT. That was Tuesday, and yesterday I woke up feeling pretty good! They say you need about 4 to 5 sessions before really feeling a difference so I will continue both twice a week until I get back to homeostasis levels!

I also started working with a Kinseologist (she’s amazing!), who performed a distant muscle testing on me and found that this is possibly attacking my limbic system, which makes a lot of sense, as all my symptoms have just shifted to my head, and eyes. Looks like I have early onset glaucoma. I’m getting a second opinion early next week, as my eye doctor is in disbelief that a healthy 35 year old can develop this. She gave me eye drop medication for now to subside the pain, but it only made me dizzy and experienced some cognitive decline. Seems any type of medication I take, I get the full range of the side effects (just like the ivermectin). I’m back to smoking weed for the glaucoma and hoping that a healthy dose of Vitamin A and Bilberry will be able to help heal it.

My Kinseologist recommended a few more supplements for me to take, as well as adding acupuncture to the alternative healing modalities.

I have faith, continuing on this path, I will have a full recovery in about a month.

So much gratitude:

Shout out to Allison, the best Kinseologist in the world…

The helpful staff at the health food store near me, helping me pick out supplements.

NY Healing Arts, the best wellness spa and healing center in Manhattan. These ladies ROCK.

Anyone who tagged me on anything and/or who slid into my Facebook messenger asking how I am, suggesting activations and meditations, supplements, healing modalities, etc for my issues. You guys know who you are!

Isabela Sladeckova for taking the time to speak with me over video chat about her personal experience which really helped!

Debbie Nalven Sulner and Ivelisse Lopez for their complimentary distance healing.

To anyone who commented on my last post and gave suggestions- I have thoroughly looked into every one, tried some, and am still open to trying others.

David Avocado Wolf and his spike protein protocols.

My two best friends who tried to warn me about the vaccine; they didn’t throw any ‘I told you so’s” in my face, and have been there every step of the way as I ask them a million and one questions about supplements.

To the many people labeled ‘conspiracy theorists’ that have figured out a way to get their information out there to help heal people that are gaslighted about vaccine injuries.

And to anyone else I forgot. Please forgive me, my brain is still healing!

Thank you, thank you, thank you, THANK YOU.

JULY 27TH, 2021 UPDATE:

Just a little update on my health journey…

Today was my last neurologist appointment.

The last thing my neurologist said to me as I left that I’ll never forget; “I’m sorry we can’t help you.”

For context, she’s talking about my complications from the Moderna Vaccine. About 2 months ago, roughly a month after my second jab, I started experiencing neurological issues that included intense migraines, swaying while walking, slurring speech, memory loss, slight confusion, brain fog and dizziness. My symptoms have since expanded to chest, jaw, and joint pain, and some deep coughing, but the neurological issues are front and center.

They had all suspected the Vaccine from the beginning, but we all did our due diligence to eliminate all issues. I personally thought I was experiencing low iron and B12 from being a vegetarian and never in a million years would have thought this was coming from the Vaccine. It was the last possible cause on my long list of root issues. I happily got a jab. I was happy to do my part and help protect others.

What they don’t tell you, is that people ARE experiencing long-term effects of it. VAERS reporting system, which is run by the CDC, reports 500k people have reported similar symptoms to mine. Common side effects include neurological issues, shingles, heart problems, and blood clots. I’m sure that’s not everyone either. Some people don’t know about VAERS to report, others don’t own or know how to use a computer, or simply some are minor and don’t know that their symptoms are linked. I would estimate the number is probably around 2 million. Still, that is a small percentage of people having adverse effects compared to the 165 million in the US that have not had any issues. This is another reason this isn’t being taken seriously.

The nurse today was so kind and empathetic and admitted to me they’ve seen an influx of people with random neurological issues that looks like its from the jab. She said she can’t believe they shove it down people’s throats and then when someone gets sick, there is no help.

The last couple of months have been a harrowing experience for me. As tests continuously came through negatively, it became evidently clear that my body (especially my brain) was inflamed and not reacting properly to the jab. I really didn’t want to believe it, but it’s the truth. And now I have no help financially or physically. Just like my neurologist said, “It’ll wear off”, “We don’t know how to heal it”, and “I’m sorry we can’t help you.”

Thank goodness for holistic methods from “conspiracy theorists.” Yesterday I had to do something really scary and take Ivermectin, a controversial drug that is said to help with long-haulers and now jab side effects. Today, my vision has improved by about 40% and I’m grateful. I’m having faith this will help heal me, along with other toxic removal protocols I’ve had to do daily just to function. I am willing to try anything to get better.

I have been trying to stay as positive as possible, but today I feel nothing but rage.

You all should have seen me this morning, I had a meltdown in the doctors office. They told me I must pay $1000 balance before seeing he doctor, and well, I did not respond well. Couldn’t keep my cool. Especially since I will receive zero financial compensation from Moderna, and no slack from my health insurance. I went off on health insurance in this country and how I was injured by the jab, and everyone in the waiting room was STARING at me.

Not my finest hour.

And that’s that. I’m on my own healing this. I will continue to do holistic methods, try new things, and just keep as positive as I possibly can, that this will, one day, just “wear off”.

Just as a disclaimer, my stance on vaccines have not changed; I have been and always will be pro-choice. Whatever you decide to do with your body is your choice and your choice only. I also acknowledge that the majority of people get the shot with absolutely no issues. This post isn’t meant to scare anyone. This post is about my truth and what is personally happening to me.

I chose to get the shot. Although it’s easy to say it wasn’t the right decision for me, it’s catapulted me into lessons and growth that is for the evolution of my consciousness. I choose to see that as winning.

But I’m sure as hell NOT getting any booster shots OR another Vaccine ever again.

With that being said, not going LIVE tonight for oracle card readings, but I have faith I will be back with these soon.

I am also contemplating recording a YouTube video about my experience. And that will be the end of this. I am SO ready to get back to my regular life.

Andrew Elphick – 70 Years Old Died Within Two Weeks of First Moderna Vaccine

March 8, 2022 in Deaths

Andrew was a healthy 70 year old, who died within 2 weeks of receiving his first Moderna COVID Vaccine.

He was a father of two special needs children.  He retired a few years ago, and spent most of his time with his two kids, who were crazy about him.

Andrew was active and loved biking and hiking in New Jersey.  He had no conditions that would have caused him to drop down in his yard, and subsequently had no vital signs when his family attempted CPR on him.

He died unexpectedly within 2 weeks of his one and only Moderna COVID Vaccine, per his family.

Greg – Severe Adverse Reactions to 1st Pfizer COVID Vaccine

March 8, 2022 in Adverse Reactions

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.”

Jennifer – Severe Lymphatic System Adverse Reactions to Moderna COVID Vaccine

March 8, 2022 in Adverse Reactions

This is Jennifer’s story:

“The COVID-19 vaccination reacted into my lymphatic system and breast soft tissue causing inflammation & pain on the side the needle was inserted.

I am putting this on Facebook so it can be shared, because mainstream media & our Government won’t make you aware. And the GP & specialist breast surgeon I’ve visited have no definitive information to provide.

So please share the post to provide awareness to other people & encourage other people that have suffered the negative impacts of the COVID jab to speak out too…

Almost 2-months ago I had my routine mammogram to get the usual all clear. I have no personal or family history of breast cancer.

Almost 1-month ago I had my 1st Moderna jab; because the Queensland Government decided to mandate the COVID jab & it would have restricted me from attending my daughter’s upcoming wedding.

Up until this point in time I was not in a rush to get the jab; because I have no health issues, I don’t take any medications & I have successfully survived the previous respiratory virus pandemic – the Swine Flu. During my Swine Flu infection I was registered with the department of infectious diseases & isolated for a month.

So I was willing to ride out all the contradicting opinions on this jab & survive COVID if I became infected with this newer variant.

I am fully vaccinated for everything else. My children are fully vaccinated. I even have the flu vaccination each year & vaccinate before travelling overseas.

I am not an anti-vaxer.

After the Moderna jab in my left arm, I couldn’t sleep for the first 3-nights because the pain was travelling up my arm into my armpit, neck & across my chest. The following days my neck, left armpit & breast continued to swell.

Seeing I’ve breast fed 4 children I know what it’s like to have your milk come in & your breasts engorge, but this was beyond that experience. Every vein in my breast was visible, I had red, hot patches on my breast, lumps everywhere in my breast & I was sitting with my extra large, very painful breast on a pillow taking pain meds and resting. And no…I’ve never had mastitis.

I tried to get to see my GP when the enlarged painful left side & breast were at their worst, but the doctor called in sick on that Friday; so the earliest appointment I could take was 4-days later.

Even though the GP had never heard of anything similar she took it seriously & sent me for an ultrasound the same day. The ultra sound showed my normal breast on the right side and my left breast full of inflammation that is currently a mass deep in my breast tissue. It was painful to scan the left breast.

Upon seeing the ultra sound results the GP provided me a referral to a breast surgery specialist who upon receiving the referral with the ultra sound phoned me & asked to see me straight away; even though he had other patients already booked; otherwise it would be another week until his earliest appointment.

The breast specialist had never seen anything like it. He’d “heard” of this reaction with the COVID jab & asked me if I had any information relating to it. So I told him about the below American Cancer Centre article; where 11% of women are presenting for mammograms after their 1st jab & 16% of women after their 2nd. He looked it up and was going to contact an American colleague to discuss.

If I hadn’t have had my clear mammogram weeks earlier I would have been one of those very worried women. Also thanks to this healthy clear, very recent baseline the doctors and I know that all this painful inflammation has been caused by the COVID jab!

So I asked the breast specialist…

Should I have my second more potent jab? And could this reaction happen even worse after it? He said that he couldn’t say because there is no information surrounding this reaction & that perfectly healthy people die after vaccinations.

So my GP is lodging the application to the Queensland Health Department to seek their direction. They will advise…

*Can I be exempt from my 2nd jab?

*Or do I have to run the roulette wheel to do what’s right for the elderly & immune-compromised, which could result in my own demise?

The GP & breast surgeon believe that because I haven’t presented to the hospital emergency near critical death from the jab that they won’t give me an exemption.

So I currently wait to find out the Queensland Government’s decision concerning my personal health & longevity… “

Allison Turner – Severe Adverse Neurological Reactions From COVID Vaccine

March 8, 2022 in Adverse Reactions

This is Allison’s story:

“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 Vaccine 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 imagining 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 breathe & 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.”

14 Year Old Boy – Severe Adverse Reactions From 2nd Dose of Pfizer COVID Vaccine

March 8, 2022 in Adverse Reactions

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.”

Young Girl With Severe Adverse Reactions After First Pfizer COVID Vaccine

March 8, 2022 in Adverse Reactions

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.”

Josh Horricks – 33 Years Old With Severe Adverse Reactions to 1st Moderna COVID Vaccine

March 8, 2022 in Adverse Reactions

This is Josh’s story:

I got my 1st shot of Moderna in June but ended up in the emergency room shortly after with an extremely accelerated heart rate, extreme shortness of breath, shakes, loss of feeling to all my extremities that all lasted 6 hrs, nearly fainting multiple times enroute.

When I brought my concerns up to the doctor at the hospital they said: “yeah heart issues are a slight side effect especially with young men but they’re very rare” and then switched to ask me what kind of heavy drugs I do and what my drinking habits are.

No refferals, no additional testing, I was just discharged wondering WTF was happening to me.

I’m healthy, fit and have never been to a hospital for anything other than a broken bone.

Miles Juneau – 31 Year Old Diagnosed with Pericarditis After 2nd Pfizer COVID Vaccine

March 8, 2022 in Adverse Reactions

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

Cienna Knowles – 19 Years Old With Severe Adverse Reactions to Pfizer COVID Vaccine

March 8, 2022 in Adverse Reactions

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

Hyperbaric Oxygen Therapy (HBOT) & Moderna Injury

March 8, 2022 in Healing Treatments

This is being re-shared from Brittney Galvin’s Instagram Page HERE

Her video below shows a significant improvement after 6 sessions of high pressure HBOT treatments.  

That is a stunning change in her live blood analysis.

britgalvin

I am SHOCKED!!!! My blood after the Vaccine

🤯 SHARE THIS EVERYWHERE!!!

I don’t even know what to say!!!

My blood has been looked at multiple times (under a scope) prior to starting HBOT and my protocol.. nothing at all phased it. It was full of clumping and unknown… things… ☠️ (correction- the first set was sampled 10/9 not 10/10)

Tonight, only 6 days into my treatment plan of Hyperbaric Oxygen Therapy after my Moderna COVID Vaccine Injury

LOOK 👏 AT 👏 THIS!!! 👏

If you are thinking twice about doing what I’m doing- STOP NOW. Just do it. Start a fundraiser. Do it however you can!

An Inexpensive, Yet Effective Treatment for COVID – Ozone Therapy

March 8, 2022 in Healing Treatments

WHAT IS OZONE?

An excerpt from the article below written by Robert Rowen:


Ozone is triatomic oxygen (O3), the most powerful oxidant found in nature. Our bodies actually produce ozone, observed in a stunning discovery at Scripps Institute [2]. Ozone therapy (OT) utilizes 1-5% ozone in 95-99% oxygen as a gas (~10-70 mcg ozone per cc gas). This mixture is called “medical ozone”. Ozone therapy has been in use since the late 1800s, but is little known. It is not patentable for profit; thus, corporate interests have no incentive to develop and disseminate it. Consequently, few formal studies have been performed. Yet many scientific articles have been published on research conducted in Germany, Russia, Italy, Cuba and elsewhere, demonstrating powerful biochemical effects. Bocci and Menendez both published books summarizing their research groups’ published basic science findings [3,4].

Briefly, OT improves blood rheology, oxygen delivery, oxygen utilization, endothelial nitric oxide production, and immune modulation via cytokine induction. Bocci privately regarded OT as creating “super-gifted red cells” with increased oxygen delivery via increased 2,3 diglycerophosphate. He thought of OT as the “ideal cytokine inducer”. His work found ozone to induce gamma interferon [5], known to be as essential part of the body’s antiviral defense [6].

When blood is treated with ozone, it instantly reacts with electron-rich double bonds of lipids and other molecules. This creates longer lasting downstream weaker oxidant metabolites called ozonides: reactive oxygen species and lipid oxidation products, inclusive of peroxides, peroxyls, alkenes, alkanes. These molecules appear to act as messengers for the key biochemical and immune modulating effects of the therapy. The Menendez Cuban group found that preconditioning animals with ozone is as powerful as dexamethasone in reducing tumor necrosis factor α in subsequent endotoxic shock [7]. This could be exceptionally valuable as a means of safely suppressing “cytokine storm”, often the cause of final lethality from pulmonary viral infection [8], including coronavirus [9,10].

Elvis and Etka summarized ozone therapy: “..effects are proven, consistent, safe and with minimal and preventable side effects. Medical O3 is used to disinfect and treat disease. Mechanisms of action are by inactivation of bacteria, viruses, fungi, yeast and protozoa, stimulation of oxygen metabolism, activation of the immune system [11].”

Ozonide drugs are now postulated to possibly remedy the growing resistance of plasmodium to artemisinin, which molecule carries a rare natural oxidizing endoperoxide bridge at its active site. Industry is searching for drugs of this class [35]. Meanwhile ozone therapy, a direct method of creating endogenous ozonides, has been utilized for a century with an excellent background of researched effects, safety, and minimal costs, depending on the method and location where administered. Ozone therapy has been reported as exceptionally safe [32].

Ozone therapy is versatile and can be used for prevention and treatment of acute and chronic diseases. Our offices treat both acute (non-hospitalized cases) and chronic viral and bacterial illnesses with ozone. There have been no reports of conflicts with standard medical care, inclusive of drug therapy. 

Dosing depends on mode of application. DIV ozone generally begins with 1100 mcg ozone (20 cc of gas at 30-55 mcg of ozone per cc of gas) with increases up to 6600 mcg (120 cc gas) as needed and tolerated by the patient. Treatment time is a few to several minutes. A more recent ozone innovation is a variant of the MAH technique, called hyperbaric ozone. Two hundred ml of blood is ozonated with 200 cc medical ozone gas at 70 mcg/cc under pressure and returned under pressure. This constitutes a single “pass” (about 15 minutes for a treatment). A common practice in Europe and American clinics is repeating this for 10 passes at one sitting (45-90 minutes for a treatment, depending on vein “cooperation”). This will deliver 144,000 mcg ozone in a single treatment session. Our clinics are using this latter method, which appears to enhance rapid recovery from Lyme disease even in antibiotic treatment failure patients. Rowen trains physicians from around the world in this method, and has surveyed them for safety. Out of a known 4,000 “ten-pass’ treatments, there were no reported significant or lasting untoward effects due to the therapy [36]. We have observed “Herxheimer” reactions, presumably due to “die-off” of infecting organisms. 

Few in our field are not familiar with the great 1918 influenza pandemic. However, few are also aware that inexpensive intravenous hydrogen peroxide was utilized by British physician Oliver, who halved the death rate from influenza pneumonia in India [37]. Similarly, another oxidation therapy, ultraviolet blood irradiation therapy, was successfully used to cure 15 of 15 cases of viral pneumonia in hospitalized patients in the 1940s [38]. Ultraviolet energy is well accepted to destroy microorganisms, and is used as a sterilizing agent, and in air purification. Ultraviolet energy destroys cysteine in microorganisms [39].

Ozone’s challenge is that it does not bring profit to justify private research to advance it towards regulatory agency “approval”, a process requiring tens of millions of USD. Hence, few in the medical field are aware of it, and fewer will consider “unapproved” therapy even to save lives [40]. It suffers from the “tomato effect” [41], because many of its achievements are regarded as impossible to believe. Virtually all use is in private offices, where most practitioners have no access to an institutional review board, now a requirement to gain acceptance of research for publication. Hence, advancement of ozone therapy into mainstream medicine languishes, and most patients, with no alternatives to conventional therapies, suffer.


FULL ARTICLE HERE

Red Blood Cells Before and After Ozone Treatments

March 8, 2022 in Healing Treatments

Rouleaux Formation Post-COVID Vaccination via Dark Field Blood Microscopy.

The dark field blood examinations seen below are examples of the blood of vaccinated patients before and after Ozone Therapy.

(1) A 62-year-old female who had received the COVID vaccination roughly 60 days earlier. 

The first picture reveals mild rouleaux formation of the blood. After a sequence of six autohemotherapy ozone passes, the second picture shows a completely normal appearance of the RBCs.

Patient’s blood with mild Rouleaux (Vaccinated 60 days prior)
Red Blood Cells were normal again after 6 Major Autohemotherapy Passes.

(2) A young adult male who received his vaccination 15 days earlier without any side effects noted and feeling completely well at the time, had the dark field examination of his blood performed. 

This first examination seen below revealed severe rouleaux formations of the RBCs with extensive branching, appearing to literally involve all of the RBCs visualized in an extensive review of multiple different microscopic fields. 

He then received one 400 ml ozonated saline infusion followed by a 15,000 mg infusion of vitamin C. 

The second picture reveals a complete and immediate resolution of the rouleaux formation seen on the first examination. Furthermore, the normal appearance of the RBCs was still seen 15 days later, giving some reassurance that the therapeutic infusions had some durability, and possibly permanency, in their positive impact.

Severe Rouleaux (Vaccinated 15 days prior)
400 ml ozonated saline infusion followed by a 15,000 mg infusion of vitamin C.

(3) A third adult who received the vaccination 30 days earlier also had severe rouleaux formation on her dark field examination, and this was also completely resolved after the ozonated saline infusion followed by the vitamin C infusion. 

Of note, similar abnormal dark field microscopy findings were found in other individuals following Pfizer, Moderna, or Johnson & Johnson COVID vaccinations.

When available, ozonated saline and/or ozone autohemotherapy infusions are excellent. Conceivably, this approach alone might suffice to knock out the spike protein presence, but the vitamin C and HP nebulization approaches will also improve and maintain health in general. Ultraviolet blood irradiation and hyperbaric oxygen therapy will likely achieve the same therapeutic effect if available.

FULL ARTICLE SOURCE

DJ Dimplez – 29 Year Old Hip-Hop Artist Dies From Brain Haemorrhage

March 7, 2022 in Deaths

According to the below video from Dj Dimplez’ twitter page, he received his second COVID Vaccine on 9/13/2021.

His death was announced on March 6th, 2022, that he passed away of a brain haemorrhage.

The Mooi family confirmed the news in a statement, saying the popular South African artist passed away from a brain haemorrhage.

“It is with deep sadness that the Mooi family announces the untimely death of Boitumelo Athiel Mooi, popularly known as DJ Dimplez. He passed away (on) 6 March 2022, from a sudden brain haemorrhage. We ask for space and respect as we process Tumi’s tragic passing,” said the family.

STORY SOURCE

Ian Matos – Brazilian Olympic Diver Dead at 32

March 7, 2022 in Deaths

According to Ian’s Instagram page, on August 4th, 2021, he got a dose of the COVID Vaccine, with the caption:

Moment of pure joy!
Alive or SUS.

According to an article published by The Sun, he had been hospitalized for almost two months before his condition worsened on 12/21/2021.

“He initially sought medical attention because of an infection in his throat which later spread to his stomach and lungs.”

His death was announced below on 12/21/21.

Tyler – 37 Year Old Father Needs Heart Transplant After Moderna COVID Vaccine

March 7, 2022 in Adverse Reactions

This is Tyler’s story:

My problems started April 26th when I got my second Moderna vaccination. I immediately developed a cough, a sore throat, and extreme fatigue. The severity of it would come and go until they end of August when I want on vacation in Hawaii. I started coughing profusely and had a sore throat. I began using an inhaler and Flonase then. It progressively got worse until they week before Thanksgiving I was coughing up blood. 

The Monday before Thanksgiving 2021, I was admitted to the intensive care unit. The doctors thought I had covid because my lungs looked like COVID lung. I had even been tested in October and was negative. They swore up and down it was COVID till the saw my heart with three blood clots in it and a failing kidney along with a failing lung. 

After 16 days I was “stable” enough to be sent home. The cardiologist at the hospital warned me I might need a transplant. On December 17th I went to the best cardiologist around and he was mystified why my heart failed. My arteries and heart have no obstructions. My heart has no scarring or swelling or and other signs of anything. The hospital diagnosed me with covid pneumonia, followed by heart and kidney failure.   My heart is only functioning at 15% and I am on oxygen. 

The cardiologist said I need a transplant and is sending me to Seattle to start the process of matching with a donor and getting on the waiting list. A transplant costs approximately 1.5 million and can be as high as 2.8 million dollars.

My share will be 20%. Plus I already have a massive hospital bill for 16 days and I will need to be in the hospital for 3-4 weeks after they transplant. 

Unfortunately I cannot afford it on a measly disability income.

Anything helps. Even a dollar. I feel horrible asking for help and a hand out. I have always prided myself on taking care of myself and family. But I literally have no other option then to lower myself to begging for money to save my life.

Tyler’s GoFundMe can be found HERE.

Jessie – 31 Years Old With Severe Adverse Reactions to Pfizer COVID Vaccine

March 7, 2022 in Adverse Reactions

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

Stephanie Whitmore – 37 Weeks Old Stillborn After Blood Clot After Pfizer COVID Vaccine

March 7, 2022 in Adverse Reactions, Deaths

This is Isabella’s story, as told by her mother Stephanie.

I want to share my story because I was All for it, I was Pro Vaccine. I spoke to all the doctors and got medical advice on what was the safest most responsible action to take in order to keep my family and baby safe.  This story is the result of professional medical doctors.

I got the first Pfizer on the 13th of September, I was 32 weeks pregnant, and I didn’t have any reactions whatsoever, I just continued with life as usual.

I had the second Pfizer on the 4th of October, I was 37 weeks pregnant, my baby was healthy and perfect through the entire course of my pregnancy and she was due any time now. 2 days after my second vaccine, I had a prenatal appointment.  My baby was in the right position and I was told everything was fine.

On the 9th of October, I noticed my baby wasn’t moving the way she usually would, and a few days later, I went in for an ultrasound and they found an Intraventricular Haemorrhage in my baby’s brain.  Which meant she had a blood clot.

Giving a still birth to my daughter was one of the most traumatic things I have experienced in my life and I would never wish this upon anyone.  I have asked my friends to please think twice if you are pregnant.  From someone who believed this was the right thing to do, I never thought this would happen to me.

I requested an autopsy and the cause was “NOT IDENTIFIED”.  I asked what usually causes it and they said, pre eclampsia, high blood pressure, thrombosis, or genetic disorders.  I did not have any of these conditions and we tested my husband for any genetic disorders, which came back clear too.

Because the doctors were unable to identify the cause, I believe it was the COVID Vaccine.  I am not sure and I will never know, but there is no other explanation.  I wish I never had it, maybe baby would be alive.

❤️ Stephanie

Isabella – Born 3.5kg, 53cm, born at 6.38pm

My little butterfly, you flew so high that now you are beside Jesus looking at us. My angel, you came to transform our lives. No words can describe the pain that I am feeling right now because I miss you so much my sweetheart. I know you are in a better place and one day me and daddy will meet you in the heavens. Everything happens for a reason and I can’t understand now the reason that you are not with me, but I trust God and I know He has his perfect plans for us. Bella my love, I promise you that I will be always close to you and praying for our Father Jesus to look after you.

My beautiful daughter I love you so much, I would do everything to have you in my arms. I miss everything about you, my darling. I miss our connection, I miss your kicks inside me, I miss the dreams and plans that I had for us. I miss what we haven’t lived but I am glad you showed me what is love. Nine months of pure love. Goodbye for now my love, we will meet you again soon. Rest in Peace.

Gabrielle – 18 Year Old With Heart Issues After Pfizer COVID Vaccine

March 7, 2022 in Adverse Reactions

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

Elle Webster – Severe Adverse Reactions to Pfizer and AstraZeneca COVID Vaccines

March 7, 2022 in Adverse Reactions

This is Elle’s story:

I had AstraZeneca back in March 2021 when it was first rolled out in 1B.  I work in healthcare and I wanted to get it because I wanted to protect my patients and myself, I was complete for the Vaccine, and figured that the risks were so rare that I’d be fine.  I had the flu vaccine every year with no issues so I wasn’t concerned.  I’m not a huge fan of needles so I was nervous getting it, the nurse was very kind and let my friend come in with me to help with my nerves.  We headed home both feeling fine and grabbed dinner before heading our separate ways.

I woke up the morning after at 2 am with horrible flu symptoms, which was fine I had fully expected that, took some Panadol and went back to bed.  I woke up to a text from my friend saying she was feeling the same so I wasn’t worried.  Next day was the same, shivering, nausea, feeling like I had the flu.. but expected it so still brushed it off.

Day three I started vomiting, couldn’t keep anything down, horrible back and stomach pain, and felt awful.  By this point my friend symptoms has disapeeared and I hoped that it meant it was nearly over.  So I left it because I thought that I was having expected symptoms as stated on the fact sheet and my friend said that she went to sleep feeling crappy and woke up feeling fine, which is what I was thinking would happen.  

It wasn’t until day 5 (Easter Saturday) that I went to my parents for Easter weekend and they saw how bad I was, my sister described me as a looking like the walking dead (charming as always!).  We agreed that we’d see how I went overnight and go to the local urgent care centre the next day if needed.  I was convinced that it was mostly anxiety at this point and that by worrying about side effects I was having I was making it worse.

Another night of vomiting continuously, and not even keeping small sips of water down my mum dragged me to the UCC.  The couldn’t run bloods as it was a public holiday and they’re only a small center but ask for a urine sample, I told them that I hadn’t passed urine for three or four days (I assumed I was dehydrated from vomiting so this hadn’t actually struck me as a concern), the immediately panicked and sent me straight to the ED.  The ED rushed me straight back, took bloods, and asked for a urine sample.. I told them the same, I hadn’t peed for about four days.  They pulled out an ultrasound machine to scan my kidneys and added more tests to my bloods.

I only remember fragments of here on as I became so out of it as I got sicker.. but the doctor said that my kidneys and liver were both failing.  Kidneys were functioning at barely 4% and my liver ALT levels were around 3900 when healthy levels should be below 30.  I was taken to admissions where they placed a catheter to confirm my kidneys were shut down and not producing urine (they weren’t) and began calling specialists to see me.  The doctor was incredibly calm through it all, explaining what was happening, how long I could expect to be in, and where I would go from here. 

My parents were warned that it wasn’t looking good and I may not make it.  I can honestly say that I have never felt so horrific in my life, my blood sugars and ketones were dangerously low and the trauma of laying there unable to ask for help as I felt myself dying will probably never fully go away.

I was incredibly lucky with the efficiency of the doctors and nurses who didn’t take any chances and made sure that I got the best care.

From here I ended up in the ICU having tubes cut into my neck and down my artery (the pain of that was like nothing I’d ever experienced) and placed on CRRT (chronic renal replacement therapy) for 20 hours, where I vomited and retched for the first four hours, before they gave me additional ondansetron to stop it.

It’s basically emergency dialysis, the blood isn’t warmed before re-entering the body, so you lay there with room temperature blood being forced back into your body shivering and shaking so violently that you end up pulling muscles all over your body even with a heated blanket over you.  This was one of the hardest parts, physically unable to stop myself from shivering and shaking until they gave me drugs to make me drowsy and I finally passed out for a few ours (by this point I was running on no sleep for a good 48 hours).

Whilst this was happening I had an arterial line placed, it took four attempts to place it as my arteries were so narrow and hard to access.  The doctor was great, but it was just more unbearable pain as the local anaesthetic wasn’t working and the four attempts were excruciating.

I was getting hundreds of scans and test run amongst everything, they had concerns about clots as my d-dimer levels were elevated but fortunately there were no obvious clots that showed up so they surmised that my body was handling any clots I may have had.  I had doctors in and out asking for more tests and trying to explain what was happening and why things were being down and what they’d show.  Every doctor I saw explained that they had to run the tests to rule out the vaccine as the cause because when they made the report to the TGA they would ask for the tests to be run.  If they hadn’t run them the TGA could reject the report.  All of the tests came back showing that I was in perfect health for my age, EXCEPT of course the organ failure.

I was initially discharged after 12 days, sent home to my parents for care and ongoing dialysis as an outpatient.  When I came in for my first dialysis (two days after discharge) I collapsed during it and had a blue code called.  I was readmitted immediately and stayed in til I no longer needed dialysis.  I spent a month in the hospital all up, receiving dialysis and being monitored before discharge home with strict instructions.

I was fortunate that after five months my kidneys and liver bounced back to normal levels, there is scarring in my kidneys but it is minimal and they’re hopeful that they won’t fail again.

Amidst all of this I ended up with severe hearing loss in my left ear, a side effect of AstraZeneca that others have reported, and whilst I can manage most days I do have hearing aids for when I’m in busier environments and manage to hear what people are saying to me.  I hate wearing them though as the noise becomes overwhelming (my ability to manage sensory input has drastically diminished, something I’m told isn’t uncommon post a medical trauma like this) and I can’t cope.  I didn’t mention the hearing loss whilst in hospital as I thought that in the scheme of things it wasn’t a big deal and thought it could have been stress.  I’ve since been told that there is a high chance it was actually an ear stroke and should have been immediatly assessed.

Following the vaccine I also developed two chronic conditions that became apparent once I was home and tried to return to my life. I’ve been diagnosed with POTS/dysautonomia and mast cell activation syndrome (MCAS), it’s had me in and out of hospital looking for answers and have led to further admissions.  I end up tachycardic everyday, on a good day it doesn’t go above 155 and on a bad day it can hit 200.  I’m constantly dizzy, off balance, nauseous, and having chest pains has become a daily occurrence.  There have been multiple episodes where my body couldn’t tolerate the HR and I’ve fainted.  The MCAS had me reacting everyday to my cats, foods and allergens would set me off.  It’s only in the last month since starting Xolair injections that the symptoms have come under control and I feel like I’m not spending my days waiting for a reaction to occur.

I wasn’t given an exemption for the second vaccine.  I was told to get Pfizer instead as I could safely have it, and this worsened my POTS symptoms to the point that I can’t manage to work at the moment.  Because of the dysautonomia my proprioception is now incredibly poor and I often fail.  I am waiting on a referral to a rheumatologist as my right leg often loses colour, gets pins and needles, and my ankle will roll and foot will drag as I can’t lift it high enough.  My physio noted that capillary refill in my right foot was drastically slower than in my left as well.  So far no one can explain why this is happening and we are hoping a rheumatologist may have answers, for now I use an ankle brace or strap my ankle to keeo my foot in the correct position and try to prevent me from falling and tripping.  I use a walking stick and walker to get around to assist with my balance, poor proprioception, and POTS.

My GP has put in an application for an exemption for the third vaccine, but I am still waiting for the government to approve it.  I don’t think that I’d survive another vaccine and another hit to my body.  But if they mandate it I will need to get it to return to my job, or make the decision to lose my job, something that I cannot financially afford when I am already unable to get up with my medical costs.

Sarah Atcho – 2016 Rio Olympian Diagnosed with Pericarditis After Moderna and Pfizer COVID Vaccines

March 7, 2022 in Adverse Reactions

This is Sarah’s story:

Obviously as you know, I’m trying to be as transparent as I can and now is more important than ever.

On December 22 I got my booster vaccination because I didn’t want to struggle with this when the season started. I was told that it was safer to get Pfizer (even though I had Moderna the first time) to avoid cardiac side effects.

On December 27 I felt a tightness in the chest and started feeling dizzy while walking up the stairs. This happened a few more times until I decided to check with a cardiologist who diagnosed me with pericarditis (inflammation of the thin membrane surrounding the heart).

I am now not allowed to get my heart rate up for a few weeks to allow my heart to rest and heal from the inflammation.

I am still doing everything I can with my coach to keep my muscles moving and he’s doing a GREAT job, thank you @patsaile !!

I have to admit that I am upset at the situation because we don’t talk enough about the side effects. I feel helpless since this is completely out of my control…

I am glad the vaccine helped avoid many deaths and reduce the pressure on the hospitals and hospital staff however I am frustrated that myself as well as other young and healthy people are suffering from these heavy side effects.

I hope you understand why it is important for me to share, I’ll keep you guys updated on the process

let me know if you’re experiencing the same, let’s help each other!

Audrey – Healthy Mother Permanently Disabled After 2 Doses of the Pfizer COVID Vaccine

March 7, 2022 in Adverse Reactions

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.

Noel – Severe Adverse Reactions From Moderna COVID Vaccine

March 7, 2022 in Adverse Reactions

This is Noel’s story:

I got the Moderna Vaccine at the end of August 2021.

Within three days I had a very severe sore and hot to the touch red/pink circle around the injection site.  

From the third day on, I experienced tingling, extreme brain fog, muscle stiffness and soreness in my left arm, neck and shoulder.

I have been unable to work since taking the vaccine and actually was put on disability due to the extreme brain fog that doesn’t allow me to even get through my daily programs on my computer.  I would be in the middle of speaking and forget what I’m saying.

On top of that, I feel tremors in my legs and arms all the time.  When I walk it felt like I was bouncing.  You could hear the tremors in my voice when I spoke.  I did get a vitamin/infusion IV within a week of having the vaccine.  It did not seem to make a drastic difference but I did start feelign a little bit better within a week.

Unfortunately I’ve been put on disability because I’m not able to work due to brain fog, and it’s severe.  I also have muscle soreness and stiffness all over my body.  One of the more interesting things I experienced during the extreme brain fog was lack of emotion.  Things that would typically upset me were like nothing.  

Sadly I used to make right under $300,000 a year, now I am fighting to get permanent disability becuase I am no longer able to work.  It is devastating and very emotional.  My doctors have continued to send me for follow ups, but only because I demand it!

When I asked my doctor to report the side effects from the vaccine, she refused because she did not want to be labeled as a whistleblower.  My side effects from the vaccine are still not reported!

I’ve had countless MRI’s, CT Scans, and so much more.  They can not find anything!  I have been going to physical therapy to try and get my physical movement back and it just doesn’t seem like it’s doing anything.  The damage is so bad that I would need to be doing therapy every single day, and naturally insurance doesn’t cover that.  I see the stuff you guys post and it just upsets me knowing there’s so many of us out there.  

I was also breastfeeding my youngest baby when I got the Vaccine and my baby started pooping blood.

My doctors did tell me not to take another one, but won’t report it as being an issue.  This is just a crazy world we’re in right now.

Emilio – Died of Cardiac Arrest 2 Months After the Pfizer COVID Vaccine

March 7, 2022 in Deaths

Emilio’s story, shared by his friend Techi:

On September 9th, 2021, My best friend Emilio took the Pfizer Vaccine.

That same day he went home with shivers and cold sweats that lasted him a full week.

Then he started getting other symptoms like swollen testicles and couldn’t pee, was retaining water.  He also kept having diarrhea and felt completely out of it.  Didn’t even have energy to eat, too fatigued.

After two months of trying to get better and being forced to stay home in bed he got a massive chest pain that made him call an ambulance. At the hospital they advised he had brain lesions and his immune system was completely compromised because his white blood cells were extremely low.

Two weeks later on November 11,2021 at 9:30 a.m he died of a cardiac arrest.

Emilio is reunited with his mom, who died when he was just a small boy. 

Emilio: “This was the worst mistake I’ve ever made.  My biggest regret.”

(This story was shared online 1/14/22.  The dates in the image below were a mistake, Emilio took the vaccine 9/9/21, and passed away of Cardiac Arrest 11/11/21.)

Stephanie – Severe Adverse Reactions From Pfizer COVID Vaccine

March 7, 2022 in Adverse Reactions

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. 

Sabrina Sandoval – 39 Year Old Mother Died of Cardiac Arrest After Stroke

March 7, 2022 in Deaths

This is Sabrina’s story, as told by her sister Erica.

I want to let her story be known.  The doctors were in shock, the nurses were in shock.  They couldn’t give us an answer as to why my sister Sabrina who was only 39 years old had a stroke and the died from cardiac arrest a few days later.  She was completely fine!

She was fine living live.  Doing her side business of selling treats.  She was at a baby shower that day and couldn’t wait to unwind.  She started just have a blank stare and completely blacked out.  She went straight to the emergency room at Hazel Hawkins hospital and there they did some scans and told her it had to do with her brain.  

She called me that Saturday around 10 PM that she was scared, but felt a little bit better just tired with a very bad headache.

She then found out the very next day, that she had had a stroke.  

We live in a small town.  Our hospital is not equipped to handle anything let alone have any doctors who specialize in strokes.  We have talked to many nurses and people within the family who know that when someone of that age has a stroke, they should have been sent to the stroke center first thing!

But they didn’t. They brushed it off and said she was fine.  She had a little trouble walking and gaining her strength.  So the hospital suggested she go to rehab.

I spoke to her every day after that week and she seemed fine.  She was her normal self, making jokes that they had given her a cheap coke and she wanted a real one.  I asked her if she wanted me to take her a real coke and she said: “it’s ok sister you can get me one tomorrow when I go home.”

She was normal and couldn’t wait to come home to her 3 kids.  She was worried about them and her husband.  She was a stay at home mom and took care of everything.  Her only worry was getting home in time from rehab for Christmas.  She sounded completely normal to me.  She only kept saying she had a bad headache which the hospital knew.

She said she was taking Tylenol.  I believe the hospital knew what was going on wanted to get her out of there.  She was a patient who was 39 years old with no history of medical issues, that had a major stroke and then complained of a constant headache.  

Later than week I got a call from my little sister saying she died.  I couldn’t even wrap my head around it.  Because I spoke to her and she was fine!  I never in a million years would have thought this!

Sabrina passed away December 8th, 2021, and leaves behind her husband and 3 children.