From the Vaccination Re-Education Discussion Forum Facebook Group!
From the Vaccination Re-Education Discussion Forum Facebook Group!
These are just a handful of the thousands of stories that have been told in our group. Consider the stories we don’t hear. Not everyone with a injury makes the connection. Often injuries like cancer, autoimmune, and dementia don’t show up for years. It is not just kids that are injured, it happens to adults too. #wedid
Vaccine Injuries aren't limited to humans - always ask your vet if he/she uses non-adjuvanted vaccines if you must vaccinate. I didn't know there was "an okay" and "a bad" rabies vaccine. I didn't know that I needed to research and ask questions. I didn't know the first vet I could get my cat to would be the cause of her pain, and of her life being cut short. I'll forever carry the guilt of wishing I had known better, done better. After a two and half year fight and two expensive lump removal surgeries, I lost my Minou to an injection site sarcoma February 15th 2020. It's taken me until now just to be able to write about it without bawling. It is believed that the aluminium used as the adjuvant in the vaccine she received, is what her body rejected. It created a lump, which then turned into a cancer, and it spread through her little body. Unfortunately it wasn’t able to be stopped by surgery and it eventually made it to her lungs. I didn't include the very graphic pictures of her lump (post removal), only her incision/stitches from the first surgery as the lump and incision from the second surgery are not something anyone wants to see. It'll turn your stomach and leave you feeling sick for weeks knowing that millions have put their pets through this without any warning that it could happen, and even be prevented. Minou was the most precious, loving, well behaved, and responsive kitty I've ever had the pleasure of knowing. Even when she was on the table the be put to sleep, she fought for her life. Twenty minutes after she was given the he paralytic, she jumped off the table. The vet told me that's never happened before, apologized and said he thought that was impossible but it was too late. The sound of her limp body hitting the floor will haunt me forever. She wanted to live and she fought her hardest, but still the rabies vaccine won. Please don't make the same heartbreaking mistake I did.
Everything was going perfect we planned the pregnancy, so I knew from the start. It was a very happy and healthy pregnancy, birth, everything. Birth was natural with no epidural. Four pushes she was out, and perfectly healthy.
She was simply a very happy baby always smiling never sick. She was Rolling over, trying to sit up on her own a little. Doing everything a 4 month old should be doing. Her Pediatrician even made a comment that she was above average on her motor skills.
Then she got her 4 month vaccines.
3 shots including 6 vaccines;
DTaP, Hib, IPV, Rotavirus, PCV, Hep B
I could feel God tugging at me to decline them. I did. I
told the nurse no. She assured me my baby was fine and would remain fine. She told me DCF could be called if any one finds out my baby isn't vaccinated, that it is medical neglect. I was so scared so I turned my back on my baby. I just looked the other way and said "fine" and she got her shots as she sat in her daddies lap. I knew in that moment I had failed her. I felt it in my gut, but I ignored it.
Within the hour our baby girl completely changed.
**She started having seizures and/or spasms.
** Screaming a horrible high pitched scream.
**She no longer smiles, coos or laughs. **Can no longer hold her head up, or sit up on her own.
**No longer rolling over.
**No longer interested in toys.
**clenching of the fists
Gradually she got worse.
**She started arching her back horribly, and trying to push her head back all the time almost touching her bottom.
**Eyes go back into her head after seconds of focusing on something, especially after a seizure or spasm.
**At times she is hypersensitive and has a spasm by just a soft rub on the face by our hands or kiss on the cheek, but not always.
**stiffness in joints, especially arms and neck.
As you can imagine we were very concerned, I knew something was terribly wrong. Our worse fear had come true.
I called the doctors they said it is perfectly normal. They told me to give her Tylenol.
I took her to see her Pediatrician for her 5 month check up. They said I was overprotective and that she is just teething, gassy and below average on motor skills. But just one month ago she was above average, that doesn't make sense. Anyways, I kept asking questions regarding vaccines or anything else just knowing gas and teething weren’t the cause. However, he was reluctant to answer.
Her 6 month appointment she was seen by a different Pediatrician. We explained all the same symptoms and concerns. She immediately picked our daughter up and checked her out, feeling her head. She then immediately referred Ariella to Joe DiMaggio Children's Hospital. Explaining that the fontanelle (soft spot on the top of her head) had completely closed prematurely.
We immediately rushed her there. They ran a cat scan to determine the cause of the fontanelle closing. Finding that the brain had stopped growing at 4 months of age, decreased in size alittle, and she has a few cysts on her brain.
So they admitted her and the tests began.
** countless blood tests
After 3 long days of constant testing they sent her home. Only to return 2 days later for an appointment for more tests.
The next 3 weeks all we could do is pray and hope for
the best, as we waited for the results. Finally they came but it wasn't good.
Her galactocerebrosidase was low. Indicating it could possibly be Krabbe disease, or another disease similar.
Now Krabbe disease is 100% genetic. Meaning both parents have to carry the gene. As well as every one else in both of our families. It is so rare the doctors that worked her case will never see it in their life again.
They said they needed to do a DNA test to confirm it. However we had to pay out of pocket. We went down to the lab payed right then and there and got the test done.
In the meantime, they are already convinced she has it and will pass soon. Advising us to enjoy our last few days with her and to make her comfortable.
They then proscribed her gabapentin and clonidine. Claiming they are both all natural, no side effects, and I couldn't overdose her if I tried.
I researched them.
Finding out -
**of course they are not natural.
**there are serious side effects including death for both.
**they proscribed her twice the amount of gabapentin my grandfather who is an amputee is proscribed.
**clonidine is not for children under the age of 3.
**gabapentin is not for children under 12.
**both slow the heart rate.
**these two mixed eventually would have stopped her heart.
So the test results from the "DNA test" came back and turns out it wasn't the DNA test they did. It was the same test he was holding the results from when he ordered the DNA test, the test that comfirmed her galactocerebrosidase was low. They did the test twice. And now claim they can't do a DNA test on her, or us. Only the fetus if I get pregnant again.
They refuse to give us answers as to why they can't do the test now. They change the subject as quickly as possible when I say it happened within an hour of her shots. My child's brain completely stopped growing, my child stopped development and lost all development she had. My child's brain shrank. And they wouldn't help me save her. They gave up on her. They tried killing her, tried stopping her heart.
They also tried putting her on hospice. After explaining to both the referring doctor and the nurse that called that we are not in the least bit interested, that we refuse to give up. They still randomly showed up and after yet again explaining we don't need the service they almost immediately started explaining the sedation process and started getting out the sedation tools, mean while my child was already sleeping. I continued to refuse it. Explaining this all started with the vaccines. Then all she cared about was whether we spoke to any attorneys. Asking us 5 times within 15 minutes in different ways. As we answered the same way each time, Stating we are only searching for doctors.
I have now discontinued going back to see them. They refuse to address the fact the vaccines caused this and We refuse to watch her die.
From research and speaking with other doctors I have found that the vaccines could cause low levels of galactocerebrosidase also. So that answers that question. I am working on getting a DNA test to role out Krabbe. I have however gotten a DNA test done showing what meds she can and cannot have based on her DNA make up.
My name is Abigail. I was injured by a vaccine and this is my story.
This is a little hard for me to share, and a bit traumatic as I go back over some of the hardest moments of my childhood. I’ve been silent about this for far too long, and now I’m ready to speak up. Although I realize this is a controversial topic, I’m asking for grace and understanding. 💜
I was born in 1998 to a loving and amazing family. My parents are incredible, and everything they’ve done for me was out of love. They’re heartbroken that I was put through so much suffering, but I hold no animosity towards them at all. If I was in their position, I probably would’ve done the same thing.
In the beginning, my parents didn’t link my symptoms to vaccines, since they didn't realize there were significant risks - they just trusted their doctor. Because I was so young, I don’t remember everything, but some things I remember clearly—especially the scary seizures.
One of my earliest childhood memories was of having a seizure. I didn’t realize what it was at the time, but it terrified me and my parents. They later described it to me as a “staring spell” because I was staring in to nothingness and wouldn’t respond to them. Little did they know that I was fighting to respond to their frightened pleas. I can only describe it as paralysis because, although I could see and hear them, I physically could not respond.
I fought, but my body refused to move, and I couldn’t force out a single sound. It was honestly one of the most traumatic things I remember as a child because I was unable to tell my parents how hard I was fighting to respond. To this day, I can still see the terrified look on my mother’s face as she begged me to answer her.
Soon afterwards, I experienced vision and hearing loss. My parents started to notice one of my eyes “wandered.” At first, they thought they were imagining it. Then one day, I remember staring at my mom and asking her why I was able to see “two mommies”. She realized something was wrong, and they scheduled an appointment with an eye doctor who diagnosed me with amblyopia.
The same goes with my hearing loss. I consider myself extremely fortunate that I didn’t lose my hearing completely. In fact, I can go without hearing aids if needed, but I still need to rely on them to hear certain tones and pitches.
I remember soon after receiving my first pair of hearing aides…I was in my mom’s bathroom with the water running and heard the rush of water out of the faucet. I told my mom that I had never heard the sound of water that way before. The sound of water was a “tone” I could barely hear.
I also started experiencing wild mood swings and would easily go on sensory overload. This is particularly difficult for me to write because I remember how I felt having little to no control over my emotions. I would obsess over the smallest of issues, becoming irrational, and often crying for hours on end over things I couldn’t control. Dealing with my “melt downs” became my parent’s new normal, never knowing when or how something would set me off crying and screaming.
Having nine other children who didn’t have this issue made my behavior all the more perplexing and clearly “abnormal.”
I was an extremely socially awkward child. I remember longing for friendship, but because of my obsessive-compulsive tendencies (OCD), I had a hard time making friends. I tended not to take social ques—I was often harsh and “bossy.”
I found myself trying to force people to do things exactly my way, without considering how they felt, and ended up hurting people’s feelings in the process. (To those who are still my friends after all of this, you’re the real MVPs. I’m so sorry that I literally forced y’all to be in my princess plays. 🙈😂)
I often complained of stomach cramps and sharp leg pains. My hair was super thin and would easily break off, I was frail, and I had trouble gaining weight.
It wasn’t until I saw a doctor who ran blood tests, that my parents discovered I was extremely intolerant to wheat. To this day, I still have severe reactions from wheat/gluten, although my symptoms have changed somewhat since then.
Over time, I learned how to deal with my challenges. I no longer experience seizures or hair loss, and I no longer have leg or stomach pains. I do still have vision problems and my hearing will never be the same, but it really could be so much worse. I’m still learning how to put others needs before my own, and to better handle my emotions and frustration, but aren’t we all?
I no longer struggle with the same issues that I had making friends, and I’m surrounded by a community of beautiful and uplifting people. I don’t ever want to take that blessing for granted.
This has been a long and painful road for me and my family, but God has been faithful through it all. I am still learning and researching ways to continue to heal, but I am on a healthy path, and I’m so, so thankful for all of it.
Thank you to everyone who has walked this road with me, especially my family. We’ve had to go through so much to get to where we are now, and y’all never gave up on my healing journey.
If you’ve been vaccine injured or have a family member who has, just know you aren’t alone. I’ve been silent for too long, but my voice matters and yours does too! Don’t be afraid to speak up because you never know if it could impact someone.
This Is my story.
I had been vaccine free untill I was 16
At age 16 I become vaccine injured after getting all my 💉
I had been a totally healthy child/teen before getting all 💉 so I could finally "be normal and go to school" (that's what my teen self thought).
Afterwards I started having asthma attacks within months of my vaccines, I get sick now even if it's small and it last forever and I can't shake it, I have allergies that I never had before.
I had been a healthy 16 year old and now sick all the time.
Years later I was given the Flu and DTap Vaccine at 34/35 weeks pregnant.
It stopped my daughter from moving or growing.
Which she had been on track before the vaccines.
We did a stress test and ultrasound and No movement was shown.
I had a csection that night. 5lb 3oz
she was given the Vitamin K Vaccine & HepB Vaccine within less then an hour of her birth.
She lost more then 10 percent off her body weight dropping to 4lb 8oz and was failure to thrive.
Thank GOD for the power of breastmilk.
For the next 2/3 months I would breastfeed every hour and then pump and syringe feed her the milk I pumped. Round the clock 24/7 for 3 months.
She never has been given another 💉
She is now almost 7 healthy and thriving.
I almost lost her then because I didn't trust my gut and do my research.
Thankfully my daughter lived.
But I have way to many friends that have lost baby's while pregnant or after birth to vaccines.
Vaccines injury and Death are REAL Not Rare!
Edited to add
It took me a few years and tons more research before I was able to put all the pieces together about my injury and my daughters.
I am happy to say I now have a almost 1 year old son that is totally totally vax free. I told them NO to flu & DTap vaccine while pregnant this time around and we said No to eye ointment, the Vitamin K Vaccine & HepB at hospital. And all other vaccines since.
He is healthy and almost 1 years old. :)
Lost him within 36 hours of receiving tdap and rhogam at my 28week appointment. ☹️
Never reported it anywhere- I￼ immediately brought it up when I was told he no longer had a heartbeat but of course was told that was impossible by the nurses and doctors ￼
Anti vaxxxxer now 😓
On June 24th 2019 my daughter was born via emergency cesarean when I was 34 weeks. I had an ultrasound at 32 weeks to check on everything since I had a low placenta, and everything was perfect with her. She was tracking beautifully and my midwife was very happy to go ahead with a natural birth.
At 33 weeks I still hadn’t had my whooping cough or flu vaccine even though I was being pressured by so many people to get it. Everything in my being said no, I was so anxious about it. Finally, I gave in and had the Tdap as I was being made to feel like a bad mum. I had family members say “you’re not protecting your daughter, if you won’t, I will”.
It breaks my heart that I gave into this bullying because the night after having the vaccine, I experienced a strange feeling. I was throwing up, cramping and called the on call nurse at 2am. They said it was most likely gastro but that didn’t make sense because my partner hadn’t had gastro. I then called my midwife in the morning, who also said it sounded like gastro. I knew something wasn’t right as I stopped feeling her the next morning. I did everything I could to make her move. My heart sunk when nothing worked, so I rushed to a local GP and had them listen to her heartbeat. As I was in the waiting room I felt her move for the first time so I honestly thought, okay you’re being a paranoid first time mum everything is fine.
The GP was able to hear her heartbeat and didn’t seem concerned. So, I continued to just push my instincts aside even though I knew deep down something wasn’t right.
I saw the midwife 5 days later and once again addressed my concerns. She agreed to have me go to the hospital for checking. My daughters heart rate was high so they decided on an ultrasound. I never could of prepared myself for what they told me. “Your daughter has had a grade 4 brain bleed and has developed a condition called hydrocephalus we need to get her out now”.
The next few months were honestly a blur but at 5 months old she is now severely delayed. She has had 2 brain surgeries, been diagnosed with visual impairment, cerebral palsy etc.
I know in my heart this vaccine caused this. My life is forever changed and now I don’t know what to do about vaccinations. In Australia, you can not receive funding if you don’t get vaccinated and can not go to schools or Kindies. Everyone dismissed my concerns and said it was 100% coincidence so I gave her the 6 week shots. She seemed to cope well with the vaccines although I noticed she started doing strange eye movements about 5 day’s after the vaccines but unsure as to if this is related to hydrocephalus or not.
What happened to her is soo rare. To have a germinal matrix bleed in utero is almost unheard of and there just isn’t any other explanation.
WESTONS VACCINE STORY
The Hero of my life is named Weston. My son was born on 100% perfect and healthy February 2, 1998 on Groundhogs day.
He received 3 DTaP, 3 Hib, 3 OPV/IPV vaccines. One set of each vaccine. He was inoculated on April 16, 1998, June 16, 1998, and August 27, 1998. We deliberately spaced out his inoculations for safety reasons. It didn't work!
We heard that the MMR was causing autism in 1 out of 168 boys so we waited an extra year to vaccinate him with the MMR and his last Hib.
On August 22, 1999 we vaccinated him. It would prove to be his last vaccination.
A year later in the summer of 2000, he was headbanging, toe walking, hand flapping and constantly screaming in a high pitch. He had constant ear infections, stomach infections, constipation, and was sick all the time, throwing up 6-12 times a week for months at a time. That is just the start. The doctor could not ever give us an answer as to what was wrong. Just to alternate Tylenol (for pain) and Morton (for fever). Unknown to us this made his condition much, much worse, and accelerated his vaccine injuries.
Unknown to us his pediatrician was destroying our Weston's immune system in slow motion and constantly telling us that all children get ill.
We enrolled him in early childhood interventions due to his delays.
On his 3rd birthday, Feb 2, 2001 we took him into a pediatric psychologist for testing. She told us he was severely mentally retarded and his IQ was measured at 43. We were shocked and totally devastated.
22 years later - Today Weston is 22 and function's at the level of a 4-5-year-old.
He requires 24 hour a day care, 7 days a week, 365 days a year, and will for the rest of his life.
He is still not 100% potty trained and requires someone to help him stay hygienically clean. He also needs help with dressing, cooking, etc, ect. EVERY aspect of life that we take for granted. And we as a family are not able to live our lives as in a normal manner nor have we for the last few decades.
PLEASE DO YOUR RESEARCH - And look at the toxic chemicals in the vaccines.
DONT BE UNINFORMED - God created us with an incredible immune system. We do not need chemical injections to build an immune system and stay healthy.
Please investigate before you vaccinate.
VACCINES ARE TOXIC CHEMICAL COCKTAILS AND WEAPONS OF MASS DESTRUCTION THAT CAN WOUND AND KILL!
Greg Wyatt Westons Dad.
Founder of AreVaccinesSafe.org
This is my personal story......
This is my son Beau.. .
Vaccine induced brain damage
He was born perfect just like his 4 brothers before him
He met all his milestones
As a mother of 5 i had absolutely no concerns with his health or development
And then over night i did
The highpitched scream
The eye turning in
He lost his few words he had began to babble
He no longer recognised us
He no longer looked when we called his name
The light behind his eyes just went out
He's now 7 and non verbal in nappies and selfharms crys and screams and smashes his head in daily !!!!
He wears a padded hat & sleeps in a padded room
I am new to the group and have a almost 15 year old son who was vaccine injured at birth from HepB.
When they placed my baby in my arms he was alert and calm. We held him for several hours, and a nurse even helped me introduce the breast which he picked up instinctually. Then they took him back for vitamin K and HepB.
When they brought him to nurse that night, he was fussy, would not open his eyes, and screamed inconsolably when we tried to nurse. The nurses said they never seen anything like this and urged me to pump and give him a bottle.
After every bottle, he would scream for over an hour and fall asleep from exhaustion. He also never opened his eyes for 3 weeks after the vaccine. We eventually switched to an elemental formula, but the screamining after eating did not stop until 3 months and a zantac prescription.
We proceeded with his 2 month vacine shots and 4 month shots. He developed fever and crying fits for days after both of those vaccines. I remember we were away with family, and my mother in-law heard him screaming all night and was shocked.
I was a teacher and had done work with Autistic children. I first became concerned when my infant would not look at my face, he actually would avert my gaze. We went to playgroups, I saw all the other infants looking at moms and smiling and cooing. My boy did not smile or coo. I researched and soon became convinced that it was the vaccines, so we stopped any future vaccines. It took us many months to find a doctor who would take my concerns seriously.
We found a researcher in Maryland who was studying signs of Autism in infants who agreed to see my son. She told me after the first visit that a 6 month old is never diagnosed, but she could tell me uneqivocally that, by 1 year old, he wouls have an official diagnosis of Autism.
Because we caught this early, our interventions were very successful. We used a preventive medicine doctor who solely treats Autism in children. We did chelation, B12 shots, GFDF diet and a host of supplements. He is mostly recovered but still presents with social awkwardness that some may label as ADHD. His exectuive funtioning is terrible, but he is in all mainstream classes and has friends.
Last summer, I made yet another mistake. He had acne and our dermatologist convinced us to put him on accutane at the young age of 14; we were not aware that this was a chemotherapy drug or that the dose he was given was almsot double the recommended dose. The drug has now fused his growth plates and, I believe, interacted with some of his old vacine injuries. His hair has thinned, he has joint pain, tinnitus, and we are waiting on blood work to see how this has effected his testosterone. I am devastated that I have been duped by the drug industry twice.
Please, if you are reading this, make sure you inform yourself of side effects before giving ANY DRUG or treatment to your children. You need to look on forums like this for annecdotal stories; just doing a gerneral search on side effects is not enough. My poor son not only has to live with an autism diagnosis, but now, because of my ignorance, he will not reach his full expected adult height and may have a slew of other permanent symptoms. We are starting a detox and are praying for the best (I am hopeful some can be reversed with detox). The guilt of this last injury is almost more than I can take; I feel like the worst mother in the world. The only thing I can do is warn others not to make the terrible mistakes I have made with my kids healthcare decisions.
This is my story, this is my truth, my purpose and my gift. I developed and Autoimmune Disease after receiving the live virus influenza vaccine (4 Live viruses) in 2013 - Within 2 weeks I daughter medical attention for my symptoms that developed that included; eczema, hair loss, IBS, anxiety, depression, and severe gastrointestinal symptoms that required treatment. That year AND in 2014 I also suffered from the worst flu’s I’ve ever had. Later that year (2013) I got a Quadrivalent influenza shot (4 weakened viruses) and my symptoms became so severe I had to have an emergency procedure. After being told I had an ‘incurable disease’ with ‘no known cause’ and would need to be medicated for the rest of my life, of which the side effects were no better than the disease(go figure). I decided I needed to find the truth and take my health into my own hands. I spent the next 7 years researching every single thing that went into my body and discovered I had a hormone responses to pregnancy as well as a sever immune reaction to the 8 viruses and adjuvants I was exposed to in 2013 and that the food products we eat trigger inflammatory responses in the body.
Since the day of my (grim) diagnoses, I’ve nurtured my body and my immune system and healed myself without the use of medication. My skin glows, my hair grows, my hormones are balanced, my body is strong, I am healthy, I am whole, I am Healed... My physician and I concluded the probability of the occurrence together and decided it was best to discuss with a specialist on a course of action.
I have been gaslighted, denied, and bullied by strangers, dr’s and nurses because I advocate for my own health and I am no longer a customer for life..
When I discussed with my specialist about my concerns for the upcoming new vaccine I was told again I could be medicated with an immune suppressant to avoid a reaction from this new vaccine.. Um what?! See how that works?! They don’t discuss the Canadian Adverse Event Reporting System or the fact that reactions can manifest after 15 minutes 48 hours or 2-6 weeks. They don’t support patients who advocate for their own health, they want to medicate us for everything so long as we’re giving our money to the cause and the cure!!
So No I won’t get Another vaccine to keep Others healthy. I will do what I need to do to keep myself and my family healthy and safe from harm! I will never again light myself on fire to keep you warm and safe in your own existence, real health and immune systems don’t work that way. I’ve been guilt baited into harming myself not once but twice. Sharing My truth, that risks are real not rare and advocating for informed consent is my way of protecting You and keeping you safe from harm, and I don’t ask for anything in return.
I am not a victim of circumstance I Am a Warrior of Experience ✨
#ulcerativecolitiswarrior #Health #naturalhealth #immunesystem #REALnotrare #healthadvocate
Nickson Pelton was born two months premature.
At his two month checkup Nickson’s pediatrician gave him eight vaccines,the 5-in-1 combo Pentacel for (DTaP, polio and Hib), Energix B for hepatits B, the pneumococcal vaccine Prevnar 13 and the oral rotavirus vaccine RotaTeq.
After his 2 month shots, his leg began tremoring. His mother was told it was no big deal. His doctor said since he was a preemie, his nerves were just getting used to working. He also ran a very low grade fever daily from the 2 month shots, even up to his next appointment.
At the age of four months,with a low grade fever upon arrival, his doctor said he needed seven vaccines during this visit. Nickson’s doctor insisted his premature birth was all the more reason he should be vaccinated on schedule.
His mother Lindsey knew this was not a good idea and protested against them. He was so tiny, weighing less than ten pounds and she was concerned about his previous reactions to vaccines. Lindsey was threatened if she didn’t allow the vaccines, Child Protective Services would be called because Nickson was born prematurely and his doctor said he needed all these vaccines to protect him. Lindsey didn’t want her son taken away so she watched in horror as her tiny little 4 month old son was given seven vaccines. The 5-in-1 combo Pentacel for (DTaP, Polio and Hib), the Pneumococcal vaccine Prevnar 13 and the oral Rotavirus vaccine RotaTeq.
Less than 12 hours later, he stopped breathing and passed away.
Read the full story here
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