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.
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.
“Gardasil is useless and costs a fortune” as well as predicting “Gardasil will become the greatest medical scandal of all times…”
Ignoring data and worldwide protest, Departments of Health within the U.S. are now sending letters to parents advising them to submit their children to HPV vaccinations. With no prior announcement, parental consent given, or notice, the states of New York and Indiana have tracked HPV vaccine non-compliers and are now hassling them with physical letters…
I am a labor and delivery nurse at Scottsdale Osborn, and studying to become a nurse practitioner. My daughter was born on December 6, 1999. She was approximately 14 years, and 2 months old when she first suffered an adverse reaction to a vaccine.
J.G. was a happy, very healthy, normal, teenage girl. All that changed when the doctor in her pediatrics office recommended she receive Gardasil as prevention against cervical cancer.
As a mother and an informed registered nurse, I was confident in the vaccination and willing to allow J.G. to be vaccinated. On January 7, 2012, J.G. received her first dose of Gardasil at East Valley Pediatrics in Arizona. She progressed normally over the next few months, showing no apparent signs of an adverse reaction to the vaccination.
On July 26, 2012, J.G. received the second shot of Gardasil at East Valley Pediatrics in Arizona. She again progressed normally, still showing no apparent signs of adverse reaction.
On January 23, 2013, J.G. received her third and final injection of Gardasil at East Valley Pediatrics.
By March of 2013, I noticed that J.G. was bruising relatively easily, but thought she was a normal teen with maybe a low iron deficiency. After all, she was growing normally and she had just started menstruating. However, J.G. had never bruised like this before, and I had never seen the bruises shaped like this before. I was concerned, but chalked it up to her being an active, growing teenager. Being a nurse, I did not see any reason for immediate concern.
However, my concern increased in July of 2013 during a vacation to Hawaii. J.G. was playing like a normal kid would and was pushed off the boat, hitting her hip against the side.
The next day, the bruise that developed looked like she had been hit super hard, almost as if someone had taken a baseball bat to her hip. I remember asking her, “How hard did you hit the boat?”
She replied, “Not that hard, I guess it’s low iron like you suggest.”
Despite my nursing background, I still did not think anything was seriously wrong.
Ultimately, at the end of January of 2014, J.G. and I went to see her primary care doctor, Dr. Chapman, for a well-child check-up. We reported to her that J.G. was bruising a lot and had been for months. We thought she needed her iron level checked.
Dr. Chapman sent her for labs. That afternoon, we had her labs drawn.
The next morning, we received a phone call. Dr. Chapman told us J.G.’s platelets were low (I believe at 23k), and she needed to see a hematology doctor A.S.A.P.
I picked up J.G. from school and kept her home until her appointment in 2 days. When we arrived to the office at Phoenix Children’s Hospital, they took more blood samples, 14 tubes, I believe, to double-check the labs and verify the diagnosis. She was again low – at approximately 24k platelets. They then asked how long we had noticed symptoms, and if we had seen bloody noses or spots on her skin. She had not at this time, just bruising.
Phoenix Children’s Hospital decided to refer J.G. to a rheumatologist named Dr. Ede and have her follow up with Dr. Shah, the hematologist. The plan was to send her labs and watch her to see what her body will do.
Dr. Ede told us during our appointment that J.G. did not meet the guidelines for Lupus, and her urine was negative for any indication of kidney damage that is present with kids with Lupus.
He did tell us that her labs were positive for something called Anti-phospholipid antibodies. This meant she was at high risk for clots. He wanted to follow her case, but felt she was not going to be a Lupus patient. He also asked that her labs be run again prior to any treatment for low platelets, such as Immunoglobulin therapy (“IGG”) to recheck the ANA and Double Stranded DNA.
J.G. was diagnosed on February 11, 2014, with immune thrombocytopenic purpura, ITP.
Dr. Shah told us J.G. would probably remain in the 30k platelet range for a few months, and would likely need intervention therapy such as IGG, Rituximab, or steroids.
The antiphospholipid issue was explained as being a possible positive as an auto immune response. The physicians could not say for sure which autoimmune condition came first, antiphospholipid antibody syndrome or thrombocytopenia.
They also said her labs were all negative for virus or other causes of ITP, and decided it was more likely a chronic immune thrombocytopenia. For several months, J.G. did stay at around 35K platelets.
Then, in May of 2014, J.G. experienced a seriously heavy period, nose bleeds twice in one day that would not stop, and little red dots all over her arms and legs. We took her to the Phoenix Children’s Hospital urgent care and they found J.G.’s platelets were 14K. (Note: a normal platelet count ranges from 150,000 to 450,000)
Dr. Williams, a hematologist with Dr. Shah, began seeing J.G. They told us to come back in the morning first thing for her first round of IGG. She was admitted all day for the infusion. They ran her blood for labs that Dr. Ede requested and started the infusion. These labs showed her ANA and double stranded DNA were both negative now. Dr. Ede decided to continue to follow her case, but did not need to see her anymore, because she does not meet the guidelines for Lupus.
J.G. came back to Phoenix Children’s Hospital for labs again to check her platelets a few days later. Her levels were around 75K. However, they quickly fell to 10K again, and she was then admitted again for another dose of IGG. Her levels rose again to 100k then fell down again to 23K.
Dr. Williams decided it would be best to start her on a medication called Rituximab to try to reverse the effects of her immune system’s response by resetting her B cells that cause her body to mark her platelets for destruction.
That night, J.G. started with bleeding of the nose again, small red marks all over her body, including her bottom, and heavy, irregular menstrual bleeding. She went to urgent care again and was told she had a 4k platelet count. The physician on call reported to the hematologist who then decided to admit her again for a high dose of steroids known as dexamethasone.
She took a super high dose of steroids for a few days to try to give her a boost while the Rituximab did its job. The steroids made J.G. very ill, with a stomach ache, headache, and racing heart. She gained some weight, too. She started the infusions of Rituximab, which is given in 4 doses for 4 weeks.
J.G. was admitted outpatient all day for those infusions and tolerated it well. She was to continue the lower dose steroids for several weeks so her platelet levels would stay above 25k. She did remain around 30K for many weeks. Then in August of 2014, her platelets jumped to over 150k. She was doing great and responding well to the treatment. She was removed from steroids. She officially completed Rituximab on June 24, 2014, and had a complete response with normal platelet count since July of 2014.
We have spent numerous hours and dollars fighting J.G.’s illness, all brought about by the Gardasil vaccination.
Worse yet, J.G. has lost her teenage years due to her debilitating condition, and cannot live a normal life. The fear of bruising and her potentially low platelet count dominates her mind wherever she goes.
J.G. continues to remain in remission, and continues to be seen by Dr. Williams every few months. During her last visit in January of 2015, her labs were rerun to show a negative DNA and slightly positive ANA and positive antiphospholipid antibodies.
Dr. Williams has said he thinks that the antiphospholipid antibodies and ANA should go away in time. However, she is still at a high risk for chronic ITP due to her age, her history of bruising post-vaccination, and the presence of other antibodies.
Her labs have continued to remain positive and her court expert Dr. Shoenfeld thinks she will remain APS positive for life. It will never go away. She will have high clot risk and the risk of return of blood related disorders and high pregnancy risk. Unfortunately it won’t go away. But so far so good. She’s still healthy.
No child should have to go through what my daughter has experienced.
This article in it’s entirety, is compliments of www.SaneVax.org
Tara and J.G., my heart aches for what you have been through. I am so sorry you have been through such a trauma and live with the anxiety brought on by an unnecessary shot.
A terrible crime by the pharmaceutical industry and government agencies that allow it.
I am so happy you are maintaining well at this time. Sounds like a lot of hoops and tests to get to this point.
You have no doubt been guided and blessed.
Stick with the guidance of the Lord and he will continue to carry you when you need it.
J.G. you are a brave girl and so positive.
Always let the Lord be your constant guide and you will always have the best possible response.
Thank you for sharing your story. Just know that another girl will be able to avoid what you have been through because of it.
There are physicians with expertise in healing from Gardasil/Cervarix/Silgard injuries.
One girl’s ovaries were destroyed, with Gardasil the only potential cause. Worse, though, is that Merck either didn’t bother to examine potential effects on ovaries or hid them—but did examine effects on testes.
The BMJ has published the case report of a healthy 16-year-old Australian girl whose womanhood appears to have been stolen by Gardasil vaccinations. She has been thrust into full-fledged menopause, her ovaries irrevocably shut down, before becoming a woman. The authors, Deirdre Therese Little and Harvey Rodrick Grenville Ward1, draw direct attention to the fact that, though the girl has been thoroughly examined and tested, there is no known explanation other than the series of three Gardasil vaccinations she had…
PROVIDENCE — Starting this fall, seventh-graders in all public and private schools will be required to get a vaccine that protects against a sexually transmitted virus linked to various genital cancers, especially cervical cancer in women.
Students who fail to get the vaccine for HPV — or the human papillomavirus — will be precluded from attending school unless their parents seek an exemption for medical or religious reasons. HPV is the most common sexually transmitted virus in the United States. It is widespread: there are more than 14 million new infections annually, according to the Kaiser Family Foundation.
Rhode Island becomes the third jurisdiction, including Virginia and Washington, D.C., to make the vaccine mandatory.
Locally, some parents are already agitating against the vaccine, saying it’s an intrusion by the government into private matters and that the vaccine’s side effects can be serious.
You may be a bit stunned and left speechless by the clip below.
Doesn’t the surgeon general’s position include health safety?
Did he mention anything about the risks when getting a vaccine if ill? Did he mention anything about the vaccine insert warnings? How about the risks of “vaccine cocktails”?
Maybe part II could include the friendly vaccine ingredients.
I bet little children would be fascinated about how the formaldehyde surrounding dead frogs, in their science classrooms, is included in vaccines or maybe the colorful blue and pink antifreeze that sprays on their daddy’s windshield is also in the “helpful” shot.
This clip is nothing short of embarrassing and I can’t help but think that the repetitive laughing, tickle-me-Elmo would have been a better puppet in this scene.
This is Laura Hayes speech at the SB277 rally that took place in Sacramento, California at the State Capitol on April 8, 2015. Cameras and editing by Joshua Coleman.
One mother, Lindsey Pelton, lost her son less than 12 hours after he was given routine vaccines. She wants to share the truth about how families are left to fend for themselves and are denied help, even for burial costs, after vaccines harmed their child. Her journey through the process of filing a vaccine injury claim will open your eyes to another part of the vaccine debate in which unsuspecting parents may find themselves.
Vaccines are advertised as safe and pushed onto the public, but no vaccine is guaranteed to be safe or effective. Vaccine information sheets state these drugs can cause serious health problems, including severe allergic reactions and death.[1] Yet, doctors mostly deny these known adverse reactions when they occur, leaving parents abandoned by their child’s pediatrician that pushed the vaccines in the first place…
