gardasil vomiting

Post Gardasil Severe Cyclic Vomiting, Migraines, and a Long List of Other Symptoms

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This is a photo of Stephanie Matthews pre-Gardasil. Below is a photo of her in December 2016, while in the hospital. She is slowly starting to let me calendar her health with photos and writing.

Gardasil, the journey no one should take…

If this story helps just one more girl, this journey will not be in vain.

I will not be able to touch the tip of the iceberg with this story. So much more has happened over these past 4-5 years. It has been a whirlwind and like a whirlwind, and unwelcome event. If you take one thing away from Steph’s story it should be clear as a bell. DO NOT GET THE GARDASIL VACCINE FOR YOURSELF OR YOUR CHILDREN.

Stephanie was 23 years old at the time of her 1st Gardasil vaccine. As most young adults, Stephanie was working, had her own health insurance and took responsibility for her health and medical decisions. Stephanie had been a Type I diabetic since age 10 and knows how important it is to take care of herself. At her regular checkup the doctor said that she needed to get this “NEW” vaccine for the HPV virus. So the journey began.

Steph received her first vaccine in June 2008. The second in October 2008. The night of her second vaccine Stephanie was hospitalized in ICU for an acute respiratory problem and sky rocketing blood sugars.

The 3rd vaccine was given in December 2008.  Early in 2009, Stephanie took a trip to Mexico. On her way back she had uncontrollable vomiting, headaches, body aches and was again hospitalized.

Thinking that she may have picked something up while on her travels to Mexico, we pressed the hospital and doctors to check for parasites and pathogens. All tests came back negative.

She began being hospitalized over and over again with uncontrolled vomiting, headaches and body aches, Test after tests, revealed nothing. Then finally a diagnosis of gastroparesis (delayed gastric emptying), from her diabetes. Her body was also full of yeast. The gastric emptying test came back inconclusive and one of them came back slow.

Here is the clincher, we did not give any thought to the vaccine, because we did not know she had the vaccine. It was not until we started realizing that her symptoms were not conclusive to gastroparesis, that I pressed Stephanie asking what she may have done differently or been exposed to. This is when she said “well, I had a vaccine”. Keep in mind she was an adult and trusting the doctors, she did not think this was relevant. They would not give her something to hurt her, she thought.

Connecting the Dots: It was Gardasil

It would be close to two years before the awakening as to Steph’s “mystery illness would be realized. It was while on my Facebook page a large flashing ad on the left of my screen shouting one more girl, got my attention. I clicked on it and found that several girls had the same symptoms. I had so many questions.

How was this vaccine tested?

What did the package insert say?

Did any other of these girls have already compromised immune systems like Steph with her type I diabetes?

Was it tested on this group of girls?

Why do some get sick but not all and why so many? It is like playing Russian roulette.

Why had other countries already taken the vaccine off the market?

This was just the beginning of the long long journey into the Gardisil nightmare.

Vomiting, Edema, Itching, Hair Loss, Extreme Moods, Jaw Growth, Bone Aches, and More

Since October 2008, Stephanie has been hospitalized over 80 times. She was in for three weeks in Southern California. This time on a purely liquid diet, hooked up to IVs, gaining weight and still vomiting.  She had headaches, disrupted menstrual cycle, large weight gain, itching, hair loss body aches depression, extreme mood changes.

She has had EVERY test over and over again.

Not one doctor that we encountered had yet to look or even consider the vaccine; they have blamed everything from her diabetes, to her being psychologically sick.

The doctors have gone so far as to say that they think we are crazy. Her last doctor in Southern California finally looked at the other girls’ stories and the website SaneVax. He threw his hands up and said, “If this were my mother, daughter, sister or aunt, I would go and get a second opinion.” Keep in mind by this time, Steph has had every blood test, scope, scan and test that was available, all pretty much inconclusive or if one came back positive once, it was not positive again.

They pumped her full of anti-nausea meds, antibiotics, fluids, painkillers, anti-fungal over and over again. Each and every hospital visit we would have to go over the same thing, and each and every time we would get the same treatment. We were always told by the hospitals,

“We don’t fix people here. We just get them well enough to follow up with their primary doctor.”

I could not get them to understand that she is hospitalized so much that by the time she gets out and gets an appointment to her primary doctor, she is sick again and admitted to the hospital. We have had 2nd 3rd and 4th opinions.

These symptoms are brutal. The vomiting is not something that stops on its own, and is accompanied by brutal stomachaches as well. Now you tell me, how does a person who is vomiting more days out of their life, than not, gain weight?

Other symptoms: It is almost like she has gone into menopause, with the hair loss, mood swings, and night sweats, hot flashes. This vaccine disrupts the entire neurological and endocrine system. In addition to the uncontrollable vomiting, her symptoms include: fatigue, fainting, dizziness, severe food allergies, missed menstrual periods, severe cramps, and bartonella rash. Weight gain, uncontrollable blood sugars, light sensitivity and heat sensitivity.

Nine Years Post-Gardasil: Still Sick, Mounting Hospital Bills and No Answers

By October 2010, Stephanie’s Cobra insurance ran out. She was now uninsured, unable to work, she could barely get out of bed, and her hospital bills had mounted to over $2 million dollars. I decided to move her to Northern California, so she would be closer and maybe get fresh start with new doctors. She had already been hospitalized numerous times in Southern California at five different hospitals.

The move north proved to us that the medical field is not willing to accept or take responsibility to go up against the “big Pharma” companies.

Steph spent most of April 2013 in the hospital. We went so far as to have her gallbladder removed, just hoping this would stop her uncontrollable vomiting, wrong again. One doctor actually told us

“So what if it is the vaccine, what are we going to do about it?”

Today, Steph is 31 she is on disability, and on Medicare, but still not one doctor is willing to look further into the fact that the vaccine has caused her symptoms. Her visits to the hospital are coming farther apart.

 

Steph Mathews 8.75 years post Gardasil
Steph Mathews 8.75 years post Gardasil

It seems that there is a series of things that happen before she gets sick. She becomes extremely tired. She will “swell up” get extremely bad migraines and body aches. Then the vomiting will start.  She will vomit with no food in her system and it will be hundreds of times and last for days. This seems to be occur every three months.

Gardasil Victims

Stephanie is not alone, there have been 394 deaths, and 51,522 adverse reactions reported to VAERS. This is only in the United States. Keep in mind; these are only reported reactions, how many other families have sick adult daughters that have not put two and two together? Many other countries are battling the same Gardasil Injuries, Ireland, Mexico, Australia, UK and Japan just to name a few.

Now they are going to be giving it to 12 year-olds in schools and without parental consent if that child wants it. And why in the world would they want 12 year olds to get this vaccine, without having to tell their parents? A 12 year old that became sick from this vaccine without parental knowledge would never be able to connect the two event! And so, the horrible journey in to Gardisil prison would begin.

I just hope that all of our girl’s stories help to get the word out that this vaccine, is a killer! It takes away lives. It makes the medical field and pharmaceutical companies millions, and now it is being said that many of these girls will become sterile. This is now being stated by the American College of Pediatricians. ACPEDS.org

My opinion is that these doctors and hospitals are scared to death to side with an extremely sick young girl, for fear of retaliation against the drug companies and mainly in this case MERCK. Please know that all 3 of my children had their childhood vaccines. I was not anti-vaccine, until this. The Gardasil vaccine “fast tracked” to the mainstream medical and do not have sufficient testing to deem them safe for anyone.

Please do not even consider this vaccine, it has damaged and killed more girls throughout the U. S. and other countries than the disease it was meant to protect against!

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Post Gardasil Dysautonomia: Nina’s Story

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Our story begins in late May of 2007. I took my daughter Nina to the pediatrician for her 12 year old checkup. During the visit the doctor proposed that I have Nina receive the first vaccine of Gardasil. I immediately told him that I was not well informed about this new vaccine. He reassured me that it was fine and better to get it while she was young. I trusted my doctor. As we left the office, I had this strange feeling come over me. I started to question myself about my decision to allow the doctor to administer a vaccine that was new to the industry. My daughter was 12 years old and what was the rush to protect her against a sexually transmitted disease?  Maybe it was mother’s intuition, but I suddenly felt sick to my stomach.

The Early Signs of Illness Post Gardasil

In early July, Nina started complaining of her hair falling out. Nina is beautiful Italian with long thick brown hair. As a mother of three, and Nina being the youngest, I often play down any medical concerns of my children until I see a true problem. I put her to ease by telling her that with her amount of hair it is common to see more of it in the shower or on the bathroom floor.

Over the next few weeks Nina started to complain of flu like symptoms. She would wake up very fatigued and nauseous. The symptoms were intermittent, but becoming more regular as the weeks passed. I did start to notice an abundance of her hair on the bathroom floor. I was becoming concerned. By August, her complaints were becoming more severe. I took her to the local Med Express and they told me she was very dehydrated and they administered IV fluids. Nina felt great and I felt relief.

The next morning, the symptoms returned. She missed the first week of the new school year. The next week I started driving her to school because she was too sick to get on the bus. The school was only five minutes away but by the time we got there she was already too sick to get out of the car. My first thoughts were maybe she was having some type of anxiety about her seventh grade. It did not make sense to me. Nina was a very active child who was always laughing and playing with friends. Her relentless love of basketball always kept her on the go. She played on three different teams.

A Mother’s Intuition

She tried to muddle her way through the first semester of school, but was losing the battle. She was becoming ill at all times of the day. She would sleep on the bathroom floor hoping not to vomit one more time. I made repeated visits to the pediatrician’s office and pleaded with them to help our child. Thoughts were running through my head as to why she became ill so suddenly. Then I remembered my mother’s intuition moment and realized our world began to change after the Gardasil vaccine. The pediatrician was in agreement that we would not proceed with the second dose of the vaccine due to Nina’s illness.

Searching for Help

The next year was filled with illness, doctor’s appointments, diagnostic tests, multiple medications, multiple diagnoses, and many, many disappointments. We were told she was suffering from, Vestibular hypo function, Meniere’s disease, tonsillitis, and last but not least, a mental illness.

My husband and I were baffled. No matter what medicine the doctor’s prescribed for our daughter, her illness continued to invade her body and turn our worlds upside down.  We finally caved in and took her to see a psychologist. The psychologist commended Nina for dealing with this confusing illness in such an adult manner. She reassured us that Nina seemed well adjusted and saw no reason for any type of treatment. How could our healthy child who played basketball 24/7 and aspired to play basketball in college dwindle down to a chronically sick child who was now on home bound study with no social life?  Most of her friends drifted away as her illness seemed invisible to them, as there was no visible signs such a blood spouting from an artery.

We then decided that the traditional medical community was not helping so we decided to try a naturopathic route. We were told it was coming form an adrenal problem and were given vitamins, detoxifying foot baths, and massage therapy know as Reiki. All were complementary, but did not give her any long term relief.

Time marched on and in April of 2009 we stumbled across the television show Mystery Diagnosis. This particular episode was describing Nina exactly. This was the first time I had ever heard the word dysautonomia. I immediately went to the internet to research this illness. I found no specialists in the Pittsburgh area. I began calling every specialist within the United States and faxed all of Nina’s medical information to their offices. We took the first available appointment from the first specialist to return our call.

Finally a Diagnosis: Dysautonomia

Nina was finally diagnosed with dysautonomia by Dr. Hassan Abdallah at The Children’s Heart Institute in Reston, Virginia.  As sad as it may sound, we were delighted to finally have a name for her illness. The pieces of the puzzle were starting to come together. Dr. Abdallah started her on blood pressure medication, followed by a vasoconstrictor medicine, followed by a medicine used for people with Attention Deficit Disorder. These medicines all help push more blood to the heart and brain, thus making her illness less violent. Typically, people with dysautonomia do not perform well in the morning.  It takes hours for their bodies to function and begin their day.  Even though we had a diagnosis for Nina, we still could not get her back to functioning like a teenager. We continued our battle by getting a second and third opinion from The Cleveland Clinic and Case Western Medical Center.  It was at Case Western that a doctor finally admitted that they had seen an increase in dysautonomia since the Gardasil vaccine was introduced.

She also takes melatonin to sleep at night. She constantly has issues with low Vitamin D which requires a prescription dose of the vitamin periodically. She takes an anti-nausea medicine as needed. She has recently been diagnosed with PCOS (Polycystic Ovary Syndrome) and insulin resistance. She combats all this by pushing herself to exercise with a trainer who specializes in strength and heart rate monitoring.

I have researched Gardasil and the facts against it are astounding.

  • Why would the FDA place a vaccine on their fast tract program (which means it only requires six months of research) if this vaccine was being administered to little girls?
  • Why are there over 2000 class action lawsuits against the manufacturers because of debilitating side effects and even death?
  • Why do the manufacturers constantly ignore the facts of websites such as Truthaboutgardasil.org?
  • Do they really think that all these people are just complainers and really don’t want to have a normal life?

We are currently seeking information about a new procedure called Transvascular Autonomic Modulation. It is an invasive procedure where they feed a catheter through the jugular vein and stretch the nerve fibers near the vagal nerve. This is said to reset the autonomic nervous system, thus giving patients relief of symptoms. It does have a 75% success rate. It is only performed by an interventional radiologist in California.

Six Years Post Gardasil

Nina was on the home bound program for high school. She never got to play on her high school basketball team. She never got to attend any proms. Regardless of the adversity she faces, she managed to graduate with a 4.0 GPA. She now attends the University of Pittsburgh at Greensburg as a full time student. She struggles through each and every day with the perseverance of a soldier. Her strength and relentless integrity to live her dreams inspires everyone who has the pleasure of knowing her. The light at the end of the tunnel is that most people with dysautonomia will out-grow it. The doctors agree that Nina’s case is severe and it may be much longer before she gets relief from most symptoms.

Lessons Learned From Gardasil

Gardasil has taught us some valuable lessons. First, never think your doctor knows everything. They are human. They work for you. If you have questions, never stop asking until you are satisfied. Always trust your gut feelings or mother’s intuition. We are better people because of this illness. We no longer take life for granted. Our days of long hours at the gym watching basketball games and striving for the most points and the biggest scholarship have been traded in for a day of no pain or a friend who cared enough to spend some time doing nothing with Nina just because she is a fun person when her symptoms simmer down. Never judge a person with an invisible illness. Everybody carries some type of a burden in their life. Lastly and most important, we trust God has a plan and we will continue the battle until his will we be done.

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Hormones MatterTM is conducting research on the side effects and adverse events associated with Gardasil and its counterpart Cervarix. If you or your daughter has had either HPV vaccine, please take this important survey. The Gardasil Cervarix HPV Vaccine Survey.

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One Less After Gardasil

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Imagine for a moment having an outgoing, vibrant daughter, just turned 21 years old – her whole life ahead of her. She’s a bright, outgoing, athletic, college student, kind and compassionate. She has hopes and dreams just waiting to be fulfilled. No parent could ask for more. All parental bias aside, this was our daughter, Brittney, before Gardasil.

When Brittney received her first Gardasil injection in June of 2007, she was told that the only real risk involved was the possibility of her having a small seizure shortly after the shot was administered. She did not react within the 15-minute window, during which the medical staff monitored her. She thought she had nothing to worry about. She admitted later, after she took the first dose, that the doctor had told her she could get the HPV viruses that cause cervical cancer through a lab accident at college, (where her blood might mingle with someone infected). She had been in a lab accident just a few months previous, so the fear of being infected was immense.

When she passed out the next morning on our family room floor, she got up wondering what had happened. Britt chalked it up to the possibility of being dehydrated. She had been quite active for several months. Several years before she had fainted from dehydration, so she didn’t think much of it. She was so unconcerned she didn’t even mention the incident until over a week later. By this point, she had experienced two other unusual episodes.

The next incident occurred nine days after her HPV vaccine injection. She had what we now know was a partial seizure. Three days later, her legs gave out while she was at a water park. Hammering pain spread up and down her legs for 15 minutes, then disappeared. As a parent, I was beginning to think the incidents were related, but was not sure how they were connected.

Britt is a fighter. She never backed down from anything, but charged head-on until she accomplished her goals. The nagging leg pain and the strange episodes of blacking out were just one more challenge to conquer. She pushed through summer determined nothing would prevent her from achieving her goal to graduate college and pursue a dream of becoming a singer/dancer.

Sometime mid-July, our doctor reassured us that what Brittney was experiencing had nothing to do with Gardasil. We were relieved – at least we could relax on that score…

In July, we took Britt to Myrtle Beach for a belated 21st birthday celebration. During this week, Brittney began to lose control of her emotions off and on. She would be completely normal, then suddenly explode. She would scream at us that we were trying to upset her, or prevent her from living her life. She had never acted this way in her life. Both my husband and I were shocked at her unprovoked outbursts. We spent the entire vacation walking on eggshells when she was present. It seemed the most innocent remark could set her off. The only thing that seemed to soothe her during that week was going to the ocean and walking the beaches.

In August, she had another ‘episode’ as the doctor called them, this time in the company of several college chums. One of them had a sister who experienced many seizures while growing up. She told Britt’s boyfriend at the time that it looked like Britt was having a partial seizure.

Unfortunately, the boyfriend would not accept this reality and shoved an inhaler in her mouth while she was unconscious and depressed it. Britt came around, choking on the aerosol. She told me about the incident later, which was upsetting. She also mentioned the incident to her doctor, but nothing more than a blood test was taken. The results showed that she was a little low on Potassium so she was told to eat more bananas.

In late August 2007, Britt received her second injection of Gardasil – again with no reaction during the 15 minutes of post-vaccination observation. But, within a week she began to have nagging issues with head pressure, like a cap with too tight of a band around her head. Over the next couple of weeks this progressed to the point where she could barely open her mouth because the muscles in her jaw were so tight. She began falling down for no reason. After three weeks, she began to experience blurred, doubled vision. She was extremely sensitive to light of any type. The pressure in her head was so intense, she was passing out daily. She developed a swelling that appeared to be filled with fluid at the base of her skull and along her spine. Along with all of the other symptoms, severe pain was raging through her body. As soon as her doctor examined the swelling, Britt was sent straight to the hospital.

Multiple tests were done, but nothing showed up on any of them. Britt was sent home with a couple of pain tablets. The resident on call felt she had some sort of brain virus and that it would go away in a couple of days.

From this point on, Brittney’s health deteriorated quickly. She couldn’t read anymore because the words seemed to run together or off the pages. She could no longer tolerate light or sound of any kind. We had to speak in whispers when near her or go up to the third floor and speak very softly. Her hearing was so sensitive that she could hear sirens more than three to four miles away and conversations several rooms away. She couldn’t sit in the same room with a television or radio on. Her pain was so bad, she cried all of the time. We bought noise cancelling headphones so she could tolerate trips to the doctor’s office. She had to have wrap around dark glasses – regular sunglasses were not sufficient to protect her from the severe sensitivity to light.

The nightmare didn’t stop there. Her face would sometimes droop to one side like it was sliding off her skull as pressure in her head grew worse. Seizures and stroking migraines began to happen 24/7. Her stomach was upset all the time. She could hardly keep anything down. She lost sensation in her legs and fingertips, she became completely bedridden, and simply longed to die.

Over the next three years, Britt was seen by over 60 doctors, including teams at Johns Hopkins Hospital, the Cleveland Clinic and the University Of Cincinnati Hospital. None of them could help her. She was so sick to her stomach, she could eat nothing but three ounces of protein drink at a time, fed with a baby spoon. Not one doctor suggested we have her stomach looked at. They simply dismissed it as being stressed, over-reacting to life, or a conversion disorder.

Just to give you an idea of what her new life is like, I will briefly touch on a few events:

  • January to March 2008 – Britt was totally bedridden and seemed to be wasting away. She nearly died before we found a doctor who helped alleviate some of her more severe issues. Unfortunately, she became intolerant of the medications that helped her. She began reacting to everything the doctor gave her. She was sent to many specialists who threw up their hands in frustration at her body’s resistance to treatments.
  • Early 2009 – We found an alternative chiropractor who recommended Okra Pepsin3 with Multizyme to help settle the lining of Britt’s gastro-intestinal tract. After several months, Britt was able to eat many organic and natural foods for the first time since her second Gardasil injection.
  • June 2009 – Brittney seemed to improve for a couple of months, including strength, but this didn’t last. By December she had lost all feeling in her legs, plus the head pressure had returned more intensely.
  • January 2010 – After being seen at Johns Hopkins Hospital Britt’s legs were put into massage bladders. This seemed to relieve some of the loss of feeling – when she left she could feel her upper thighs again. By spring, she was working with a researcher who was willing to try to help with some of Britt’s other issues. He suggested CoQ10, vitamin K Complex, magnesium, calcium and Vitamin D3 supplements. Britt’s sensitivity to light and sound diminished and some of her pain was alleviated. She had a boost of energy for the first time in three years.
  • April 2010 – A migraine specialist administered pain blocks to the back of her head (scalp) which relieved a great deal of the head pressure, jaw pain and complex migraines. She began to eat better.
  • June 2010 to January 2011 – Brittney seemed to be doing well. An alternative doctor had made some modifications to her diet that seemed to mitigate some of her more severe symptoms. She began a gluten-free, casein-free, sugar-free diet, avoiding Citric Acid, MSG, artificial preservatives, and mushrooms.
  • January 2011 – She was exposed to a virus. Her immune system could not handle it. She physically collapsed. The doctor told us that her immune system was crashing and he couldn’t help her. Britt’s grandmother sent over what we thought was homemade chicken with dumplings to boost her health. Brittney gained 60 pounds during the following 24 – 30 hours. We discovered there was Citric Acid in the broth. Nothing would bring the swelling down but time.
  • May to June 2011 – Her more severe pain symptoms calmed down a bit, but she was still vomiting. Her abdomen and stomach swelled to the point where she looked like she was six months pregnant.
  • 2011 – We finally found a gastroenterologist who was willing to examine Britt’s stomach. She was horrified at what she found – Gastroparesis – a damaged Vagus nerve in Britt’s stomach which prevented normal digestion and emptying of her stomach.

Last summer, 2012, we started taking Britt to another alternative doctor. Gradually Britt began to have a small semblance of the life she had before Gardasil. After months of IV treatments, she has been able to handle a large crowd at a cinema, a very busy restaurant, and even go to the mall briefly. Understand that these events have taken place weeks apart. She still has a long way to go. She has been able to enjoy her favorite music with the speakers “normal” without suffering. She wears her wrap-around low vision glasses only on very bad days. She is able to walk on her own for short distances despite the lack of feeling in her legs.

January to April 2013 – Britt has had a huge setback which we believe was triggered by an LH hormone test. This test was to check the levels of these brain-based hormones to try to regulate them. She felt like the Gardasil nightmare was starting all over again before the hormone was neutralized. Within days of the test she began a slow increase of seizure activity, which built from a couple over a four month period, to multiple, daily events. Some were so severe that her power port shifted under her skin. After four weeks of non-stop seizures, we were able to get her in to the doctor’s office for a much needed IV. It took her nurse three tries to find, then flush the port, before the IV therapy could begin. Her seizure activity has now slowed to a minimum. As long as she stays on track for the IV’s, (basic vitamin/mineral infusions that help boost her immune system, calm physical issues, improve mal-absorption of nutrients), she can maintain much of her homebound activities. There are still periods when we talk with her that she displays signs of confusion, memory loss, and inability to concentrate.

Brittney has been ruled “Disabled” due to residuals of Gardasil by the SSA. She receives some compensation through the SSI which is helping pay her myriad medical bills.

Nearly six years ago, Gardasil changed our lives forever. It has been a nightmare without end watching our daughter suffer through every stage of the past several years. She has literally become ONE LESS!

 

Hormones MatterTM is conducting research on the side effects and adverse events associated with Gardasil and its counterpart Cervarix. If you or your daughter has had either HPV vaccine, please take this important survey. The Gardasil Cervarix HPV Vaccine Survey. 

To take one of our other Real Women. Real Data.TM surveys, click here.

To sign up for our newsletter and receive weekly updates on the latest research news, click here.