BY AND
“Programs in countries around the world have begun quietly compensating people who have been injured by or died as a result of the COVID-19 vaccines.”
Category: vaccine-injured
HPV vaccines: My Daughter’s Lost Years
By Fiona Mackenzie, Cromdale, Grantown on Spey, Highlands of Scotland
Chelsea had 2 injections of Cervarix in the fall of 2012 before we went to Australia. A few months after we returned, we took her in for the third jab. The GP practice stated that they didn’t stock Cervarix any longer, but would check whether they could use Gardasil to finish the series. The next week in May 2013 she had her final vaccination, but it was Gardasil, not Cervarix. I did not question this because I trusted the doctor to protect her health. However, looking back I had so little information to go on at the time, I certainly should have questioned the decision to mix the two HPV vaccines. Until after the third injection, Chelsea was a normal healthy girl.
In late August of the same year, she started complaining of back pain. At first, I discounted it but 3 weeks later it had become so serious we had to take her back to the doctor. She was referred for physio, but it did not help. As time went on, Chelsea became increasingly disabled by her now constant back pain.
By late September she could not manage to get out of bed very often. School attendance became impossible as the pain spread to other joints in her body, mainly her neck, knees, and legs. We were now regular visitors to our local GP. Chelsea was referred for an urgent MRI. The results returned 5 days later showing mild edema on her anterior spinal column. Her GP suspected Lyme disease, but the test results came back negative.
On December 3rd, 2013, Chelsea’s GP admitted her to the Children’s Ward. Her symptoms at the time were a persistent pain in her back, lower and upper limbs, sleeping problems, loss of grip strength, paraesthesia (tingling, numbness) in her hands, intermittent tingling in her arms and legs, and no reflexes. During her 4 day stay, Chelsea had various specialists trying to find her reflexes but all were unable to do so. She also had a lumbar puncture, nerve conductive studies, and blood tests. The doctors reported that nothing of great interest was found.
By this time, Chelsea had not been in school for more than 3 months and was able to complete only small amounts of regular schoolwork at home.
The next few months Chelsea spent in bed. If I took her out, she would have to use either crutches or a wheelchair. She was in constant pain and being treated with a cocktail of Amitriptyline, Ibuprofen, Solphadol, and Dihydrocodeine.
By February 2014, she also developed headaches during which her eye became swollen so the GP added an anti-migraine drug (Pizotifen). Chelsea also struggled with dizziness and developed strange food intolerances.
Things finally started to improve a bit by April 2014 so Chelsea was able to return to school for 2 hours a day.
Later in April, she saw a different GP who changed her cocktail of drugs because the doctor felt Chelsea must be “drugged” and this was not helping her. Around the same time, she began taking advice from and being treated by a homeopath. Chelsea decided for herself that the only true way to detox was to stop her medications. This seemed possible because her symptoms decreased as she removed various prescription drugs from her daily medical cocktail.
By June, Chelsea had improved enough to be able to return to school for the mornings. Her most recent MRI scan showed that she no longer had swelling on her spine and her general health was somewhat improved. She was now in year 4 in school but had missed all of year 3 with the exception of a few hours. She still had daily pain and various strange symptoms, but she learned to cope with them. We were still having follow up medical appointments on a regular basis.
We never obtained an official diagnosis for Chelsea – which has hugely affected her life. Having no formal diagnosis made her feel like no one believed her symptoms were real. When the medical professionals kept telling her they could find nothing wrong, I am sure there were times when she questioned her own sanity.
There is no doubt in my mind that HPV vaccines played a part in changing my daughter from a healthy young girl into one who was constantly sick with a long journey to recovery. After all, the only change in her life prior to the appearance of all these new medical conditions was being vaccinated with Cervarix and Gardasil.
Fast forward three years to September 2018: Has my daughter recovered? Has Chelsea regained some sense of normality in her life? The answers to these questions are both “NO”!
Chelsea has had to battle mental health problems. I strongly believe these issues stem from the long-term chronic illness she had to endure during her teenage years. These years changed my daughter’s entire outlook on life. I rarely understand her reasoning with things. At times I despise her ways. However, writing her story has made me stop and think. The happy go lucky girl I had pre-vaccine is probably gone forever.
Would she have developed mental health problems had she not had the HPV vaccines? Unlikely, I expect. Spending so many of your teen years bed-bound with no real support from the medical community most definitely takes its toll. Chelsea was a bright scholar in primary. She was advanced a year in reading and took great pride in her 100% attendance record. She has the certificates to prove that. She walked out of high school in the 6th year with only a few Nat 5 as she had such poor attendance. She was so unwell she could not manage 1 higher.
Today she still suffers multiple symptoms, including endless lethargy and suicidal thoughts. Chelsea is now an unhappy 19-year-old without much focus. This young lady readily admits that during her illness she felt virtually abandoned by the medical profession.
As her mother, I cannot help but believe her current mental issues might not be so profound had she felt supported and cared for by those who were supposed to help her heal.
Thank you for taking the time to read this. Quite honestly, it was not at all easy to write the story of our life over the past few years. Doing so brought a flood of emotions back to the surface.
Instead of watching with pride as Chelsea worked to achieve her hopes and dreams, our family fought to cope with all of her new (and still unexplained) medical problems. Instead of celebrating the milestones teenage girls typically experience during high school, our family spent these precious years feeling abandoned and betrayed by a medical system we trusted to care for her health and well-being. We suffered along with Chelsea as her youthful enthusiasm turned to bitter despair. We would give anything to be able to turn back the hands of time.
Unfortunately, our family is not alone. Families around the world are experiencing similar events after HPV vaccinations.
When is it all going to end? When are people in the medical profession going to have the courage to stand up and fight for our children?
This article in it’s entirety, is compliments of www.SaneVax.org
Young Boy Died of Myocarditis After Pfizer Vaccine, Says CDC Before Signing Off on 3rd Shot for Kids 5-11
By
The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,277,980 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and May 20, 2022, to the Vaccine Adverse Event Reporting System (VAERS). That’s an increase of 9,972 adverse events over the previous week.
VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.
The data included a total of 28,312 reports of deaths — an increase of 171 over the previous week — and 232,694 serious injuries, including deaths… Continue to the Article Here
Brianna: Surviving Post-Cervarix Syndrome#Parent#Vaccines#HPV
By Laura Price, Newport Pagnell, Buckinghamshire UK
Brianna’s life after Cervarix
My daughter, Brianna, was an active dancer since the age of 2 and a member of the school athletic team. She has always been fit and healthy and very academic.
On September 28th 2011 at age 12 she had her first dose of the Cervarix vaccine. Shortly thereafter everything changed.
During the next 3 weeks she became increasingly unwell, experiencing fatigue, insomnia, constant nausea, increased body temperature, hot flushes, headaches and muscle and joint pain. She would attempt to go to school, but they would just send her home.
Her GP carried out several blood and urine tests, but all results were negative. We asked the GP could it be a reaction to the vaccine. Our GP contacted the manufacturers who confirmed that her symptoms were recognised reactions, but not generally after this length of time. However, our GP advised that she should not have the 2nd and 3rd doses of the vaccine in case.
Over the next 6 months Brianna could not handle more than 1 or 2 hours a week at school, some weeks there was no attendance. She also had to give up all sports and dancing.
To learn more about this period of Brianna’s life, read her original story here.
Post-Cervarix Syndrome: The next few years
In April 2012, after seeing the Paediatrician at our local hospital, she was referred to Gt Ormond Street Hospital to see the ME specialist team led by Dr Vic Larcher. It was then she received a diagnosis of CFS/ME (chronic fatigue syndrome/myalgic encephalomyelitis).
When we asked him if the vaccine could be the cause, his simple reply was, “I am treating a lot more girls with CFS/ME since its introduction.”
Since then treatment has been regular physiotherapy and for 18 months she had psychology to help her deal with having a chronic condition.
Brianna now has to take 20mg of Amitriptyline a day to help her sleep at night, co-codamol every day for pain relief and anti-nausea medication as and when required. She has also been having hydrotherapy and is currently waiting to get a TENS machine for pain relief.
After two and a half years, Brianna could manage to attend up to 11 hours of schooling a week. She has been further diagnosed with Raynaud’s disease, hypermobility syndrome and postural hypertension.
Brianna has a very small circle of 4 close friends, having lost a lot of social contact due to not being well enough to attend school and do all that other healthy teenagers do. This serves to make her feel even more isolated.
By February 2016, Brianna successfully gained high grades in 7 GCSE’s after a part-time timetable at school and a lot of self-teaching at home.
She now attends the 6th form and is studying 3 (the norm is 4) A-levels over a 12-hour week, only going in for lessons and doing all study periods at home. However, it is not often that she manages the entire 12 hours.
She still has a small circle of friends. Due to the increased work load at school, we have to keep an eye on social time to ensure she does not overdo things and miss important time in school. She tried to start dancing again, but unfortunately had to stop as she was finding it too much to handle.
She still has regular physiotherapy to work on increasing her exercise time. She had a goal of being able to go on a school trip to Barcelona in July of this year and the school would only let her take part if her physiotherapist confirmed that she was fit enough. She did manage to go, however, it then meant she missed the week of school after her return, as she was so tired.
Brianna continues to take amitriptyline to help her sleep at night and attends hospital in London twice a year to be seen by a CFS/ME consultant who monitors her progress.
She has passed her driving test and has her own car, which is a great help in preserving her energy levels and enables her to easily get to and from school.
We have been looking at further education at University, but at this stage Brianna really is not sure if she would be able to cope.
She spent a lot of time trying to find a part time job, like her friends have, but it was very difficult to find something that she could cope with without over doing it. She now has a small job helping in a local hairdressers and they are very understanding of her condition and work around the hours she can do.
We would love her to have a normal teenage life.
A Letter From Robert F. Kennedy, Jr. and Robert De Niro to American Journalists#Real#Vaccines#Autism
By Robert F. Kennedy, Jr. and Robert De Niro
On the occasion of our announcement of the World Mercury Project’s $100K challenge, we want to address America’s reporters, journalists, columnists, editors, network anchors, on-air doctors and news division producers.
We especially want to reach out to those of you who have made a point of assuring the public about the safety of the mercury-based preservative, thimerosal. It’s our hope that this challenge will elevate this important debate beyond name calling and prompt a genuine examination of the relevant science. The American public is entitled to an honest, probing and vigorous discussion about this critical public health issue—a debate based on facts, not rooted in fear, or on blind faith in regulators and the pharmaceutical industry.
We are both pro-vaccine. We need to say this at the outset to contravene the reflexive public relations ploy of labeling every vaccine safety advocate “anti-vaccine.” As the British Medical Journal pointed out last week, that epithet is a derogatory attack designed to marginalize vaccine safety advocates and derail reasoned debate:
“It stigmatizes the mere act of even asking an open question about what is known and unknown about the safety of vaccines.”…
Flu vaccination ban goes national after fever, convulsions in children#android#iPad#retweet
Chris Thomson
Seasonal flu vaccinations across Australia for children under five have been suspended after 23 children in Western Australia were admitted to hospital with convulsions following their injections.
One child, aged 1, remains in a coma in a Perth hospital.
He couldn’t cry – his head was hanging down in the car seat and he couldn’t move. I was petrified – it was one of the worst experiences of my life.
Commonwealth chief health officer Professor Jim Bishop yesterday announced the suspension while authorities urgently review data from around the country.
WA’s chief public health officer Tarun Weeramanthri has defended the response time in closing down the state’s juvenile flu vaccine program amid revelations that children were presenting with convulsions more than two weeks ago…
Americans are Talking About Vaccines#android#iPad#retweet
by Barbara Loe Fisher
How many mothers do not witness a child’s vaccine reaction and never understand why their children whose physical, mental and emotional health suddenly regressed after vaccination? How many of those children are filling the special education classrooms, doctors’ offices, mental health facilities, and prisons in America?
What happened to my healthy son after vaccination in 1980 sent me on a journey to learn more and find out why doctors are not talking about vaccine risks, and why a commercial product that can brain damage and kill people is being mandated. In part, I was driven by disappointment in myself. As a college educated woman, who had come from a family of doctors and nurses, and had worked as a writer at a teaching hospital before I became a mom. Why did I irrationally assume that vaccines were 100% safe and effective? Why had I blindly trusted a doctor instead of examining vaccination with the same due diligence that I had researched nutrition and toxic exposures during pregnancy and had taken prepared childbirth classes to weigh the merits of an epidural versus natural childbirth, and breastfeeding versus bottle-feeding?
Some of my questions were answered during the two years of research that medical historian…
http://www.thevaccinereaction.org/