New Gardasil Horror Story from the UK#android#iPad#retweet

[SaneVax: Author Bryan Hubbard tells the story of a young girl from the United Kingdom who’s life changed dramatically after the administration of Gardasil. A huge thanks to Bryan and the staff of What Doctors Don’t Tell You for giving SaneVax permission to share the following article which will appear in their June issue.]

My Horror Story

By Bryan Hubbard, What Doctors Don’t Tell You

We believed them when they said the HPV vaccine was safe
We believed them
when they said the
HPV vaccine was safe

Lotte Amit has not lived a proper life for two years since she had the HPV vaccine against cervical cancer. Tragically, her story is one of a growing number that suggests there is something terribly wrong with the vaccine

Charlotte (Lotte) Amit never had the MMR vaccine. She suffers from hyperthyroidism (an overactive thyroid gland) and her parents, Sue and Ian, thought it best not to vaccinate. But they didn’t have the same doubts when they received the standard letter from the local doctor’s surgery for Lotte to have the human papillomavirus (HPV) vaccine against cervical cancer.

“Certainly, we were surprised to receive it because Lotte was only 15 and she definitely wasn’t sexually active. I queried it and they told us it was a safeguard for the future. We had complete faith that this was for her good, and that it was safe and that the doctor knew what was in the vaccine,” said Sue, of St Austell, Cornwall.

Lotte had the first two of the three-course Gardasil vaccine in the autumn of 2012. After the second jab, she started spinning her hands around for several minutes. She kept complaining of tingling in her hands and wrists. It reminded Sue of the behavior she regularly witnessed in the special-needs children she cared for as a care agency director.

This strange behaviour lasted for only a couple of days, so Lotte was given the third and final vaccine the following year, in March 2013. Two days afterwards, the nightmare began, said Sue. Lotte would roll around on the floor for 10 minutes three or four times a day, screaming with the pain in her hands and feet. Ian and Sue gave her painkillers, but they didn’t seem to help.

Lotte, who had always been a vibrant and energetic girl, suddenly became very lethargic and couldn’t get out of bed, and would sleep for the entire morning. Her periods stopped abruptly.

She also developed a strange obsessive–compulsive problem: whenever anyone sniffed, she felt excruciating pain in her hands and feet. This got so bad that she often ran out of the house at all hours of the day or night, once when she was naked.

The local police eventually found her hiding in some woods. “Looking back, I think some association built up when someone sniffed while she was in pain,” said Sue. Sue and Ian said it was “painfully obvious” that the HPV vaccine was to blame. They took Lotte to the family doctor who had administered the jabs. “He just told us to get on with it,” said Sue. Convinced that Lotte’s problems were a form of hysteria, the doctor referred her to a psychiatrist, who prescribed antianxiety drugs, including Risperdal (risperidone).

One evening, Sue was lying against Lotte’s chest and noticed she had an irregular heartbeat; using a heart monitor, she realized she was skipping four beats out of every 10. Doctors at an emergency unit told them she had a systolic heart murmur, which wasn’t life-threatening.

They also took her to a local homeopathic clinic, where the homeopathic toxicologist there told them that Lotte’s nervous system, ovaries, kidneys and liver were damaged. He treated her for several months, and Sue noticed a big improvement in Lotte.

He also advised Lotte to start drinking spring water, as the silica in the water binds to aluminium, which was one of the ingredients of the vaccine. After drinking several litres of water every day for a few days, Lotte had her first period in a long time. “I think she has had three proper periods in two years since having the vaccine,” said Sue.

Sue had to pull Lotte from school last year just three months before she was due to sit her GCSE exams, and have her hometutored. She ended up with five low-grade GCSEs, and got a D for her science when she had been predicted a B. She started college last September, but had to leave because of her phobia of hearing people sniffing. Lotte is now studying ancient history and classical archaeology at home as a distance-learning student.

Today, Lotte, 17, is learning to cope with her phobia, and Sue says she’s showing signs of some recovery, although nobody knows if she will ever fully recover or even be able to start a family of her own. “While we’re extremely angry that Lotte’s life was almost ruined by the Gardasil vaccine, we’re just thankful she’s not permanently in a wheelchair or dead, which we know has happened to too many young girls who were given the HPV vaccine, having been told it was perfectly safe.”

Read What Doctors Don’t Tell You here.

This article in it’s entirety, is complements of www.SaneVax.org

Lotte, you are a very brave girl and thank heavens you have such supportive parents.

I am so sorry you are having to go through this complicated and painful ordeal.  You will undoubtedly help other kids from enduring these pains through sharing your story.

What a good move to attend a homeopathic toxicologist.  It is great to hear that you and your parents are searching for the best healing modalities for you and the success you are receiving.

I have a menu option on my site called Featured Doctors. 

You will find that I have links to various health practitioners with experience in this area.  Many times distance is not an issue.

Below is a link to additional practitioners with experience in this area as well.

SaneVax medical professional listing

Your diligence and determination is an inspiration to me and many others.

I know as you continue trekking forward, and keep the Lord by your side, that you will not be alone and you will see beautiful things happen. 

It might be hard to say that now, but the hardship you face will become easier as you see His hand in your life.  He loves you and will help you.

Here is a musical piece that I hope you enjoy.  God bless, and keep your sites on Him.

your friend jen.

Warning: Gardasil injuries can have a permanent impact#retweet#Vaccines#HPV

By Annette, Melbourne, Australia

vaccine science?

I write our daughter’s story to give you an idea of the permanent impact Gardasil injuries can have on a young girl’s life. My daughter has battled her injuries for over 5.5 years. Thank you for taking the time to read her story.

Before our girl got sick she was a high achieving student, an active member of the Student Leadership Council, a Scouts girl and a fantastic field hockey player. She got sick after receiving 2 Gardasil vaccinations in the beginning of 2009.

She has a Vaccine Injury and has officially been diagnosed with Chronic Fatigue Syndrome/ME, Hypotension (low blood pressure) and Tachycardia (high heart rate when standing up, to pump blood to brain), also called POTS.

At the moment, she still suffers from (extreme) fatigue on a daily basis, headaches (especially end of the day), her hands are sore with nerve pain and she lives with daily joint and muscle pain. Her ears pop every time she swallows and she has trouble hearing. She has difficulty concentrating when there is noise around her. Her feet are always cold but she doesn’t feel it. And that isn’t all of it…

Her days vary; one good day doesn’t mean the next will be ok. One good week doesn’t mean the next week might be better. Sometimes her symptoms come on quickly. A severe headache can appear in a couple of minutes.

In the last 5.5 years our daughter also had to deal with fatigue that made her a couple of times lay in bed fulltime for (6) months in a row, a constant (excruciating) headache that lasted 2.5 years (!), sore throats, swollen glands, chest pains, dizziness with black outs, weakness in her legs making it unable to walk without assistance, abdominal pain, muscle pain, brain fog, trouble concentrating and short term memory and gastro-intestinal problems. She picked up every bug that was around and had high temperatures about every 4-5 weeks.

After 2.5 years of being sick (and no doctor or specialist knowing what to do to help her) our daughter deteriorated so much that we almost lost her (mid 2011), she was too weak to talk, or even eat and drink. Her body was so toxic that her organs were shutting down. For months we were afraid to go into her room in the morning….

Neuro training, brain training, osteopathy, detoxing, a strict diet, supplements and more alternative treatments all helped to improve her health.

We have seen great results; she has had a couple of fantastic months…. until a relapse happens. We have also seen her deteriorate very quickly to being fulltime in bed again around September/October in the last three years. Each time this happens it is hard to get healthier again.

Because of being sick our girl missed about 3 years of her schooling. She wants to be at school but her body doesn’t always let her, which is very disappointing every time it happens. There are many times she needs to spend all her energy on catching up with school work. Through all of this she still wants to finish high school with year 12 and study at a University (she is interested in Political Science).

Next to missing out at school she struggles with her social life. She is lucky to have a couple of friends that have stood by her from the time she got sick, but a lot of people don’t understand. She always worries if people will understand her limits, when she isn’t able to stay in touch because she is just too exhausted or when she needs to cancel last minute. She is now 18 and still can’t do sport or a hobby next to (part time) school. She is not able to get a regular job to make some money like most of her peers.

Besides the physical illness, the stress of not knowing if she would ever get better, of not having a “normal” life, of disappointment after disappointment, of people not believing you, has been enormous, not only for her, but also for her younger sister, my husband and I. Gardasil changed our lives completely, we have learned to appreciate the little things in life.

We are very proud of our daughter and admire her way of handling all the challenges in her life. She has become mature very quickly in certain ways, but she has missed out on lots of experiences as well. We still fight hard to make her health improve more, we hope she will stay good for longer than a couple of months and keep our fingers crossed she will be able to accomplish everything she is dreaming of…

Through sharing our daughter’s story I hope that people research before they say yes to the unnecessary Gardasil vaccine. We trusted the system and thought we did the right thing, but the system has failed us.

Nobody wants to take the responsibility when this happens to your child. This “one solution fits all” system needs to change.

Please go to www.sanevax.org, or the Facebook groups set up for families injured by HPV vaccines. Do some research before you decide if Gardasil is a good choice.

This article in it’s entirety, is compliments of www.SaneVax.org

Annette, I feel at a loss for words after reading the enduring trial you, your daughter, and family are living.  I ache for the lack of attention, and support for your family.

It’s ludicrous to have millions poured into marketing these girls, on their favorite channels, at school, and so forth, and then silence when they are injured by the Gardasil/Cervarix vaccines.  It’s a tragedy, and I hope, and pray that your silence is lifted, and you are received by loving arms of those who know what to do in these circumstances.

You have proven strong, and dedicated, and I Know that many will receive guidance, and warning through your words.

I am grateful that you have found the kind, and educated folks at SaneVax Inc.  They will have good advice, and I as well have a link to doctors that are experienced in this area.  Distance in most cases is not an issue.  Here is the link to my, Featured Doctors.

I know as you trust in your Father in Heaven, he will continue to guide, and bless you. 

I have little to give, but here is a musical gift that I hope you enjoy, and find some respite at this time. Your friend in truth, jen.

 

Gardasil Changed Our Definition of Normal#HPV#Android#Vaccines

By Francine Pugliese, Pittsburgh, Pennsylvania

Nina is the youngest of my three children. I had no idea a trip to the pediatrician’s office for a checkup and one simple injection could change our lives so drastically. For the last seven years, our daughter has fought to regain some semblance of her normal life.

7 years of post-Gardasil nightmare

Spending long hours at the gym watching her play basketball and dreaming of sports scholarships have all been traded in for one simple wish, a pain free day for Nina. I continued to pray that, despite her daily illness, her childhood friends would still find Nina to be that funny, animated girl that could make anyone laugh.

Our story began in late May of 2007. I took Nina to the pediatrician for her 12-year-old checkup. During the visit the doctor recommended that I have her receive the first dose 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, a strange feeling come over me. I started to question my decision to allow the doctor to administer a vaccine that was new to the industry. My daughter was 12 years old. 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.

Early Signs of Illness Post Gardasil

Less than a month later, early in July, Nina started complaining of her hair falling out. As a mother of three, I often play down any medical concerns my children have until I see a true problem. Nina is a beautiful Italian with long thick brown hair. 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 more severe, so I took her to the local Med Express. They told me she was very dehydrated and administered IV fluids. Nina felt great afterwards. I was relieved.

Unfortunately, the next morning the symptoms returned with a vengeance. She missed the first week of the new school year.

The following 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.

At first I thought maybe she was having some type of anxiety about starting seventh grade, but that did not make sense to me. Nina had always been a very active child who was constantly laughing and playing with friends. Her relentless love of basketball kept her on the go most of the time. She played on three different teams. School had never been a problem for Nina.

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 pleading with them to help our child. Questions were running through my head constantly. Why did she become so ill so suddenly? What could have possibly happened? What had she been exposed to that could have caused her mysterious symptoms?

Then I remembered my mother’s intuition moment and realized our world began to change after the Gardasil vaccine.

Her pediatrician was in agreement, 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 doctors prescribed for our daughter, her illness continued to invade her body turning our world 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 homebound study without a social life?  Most of her friends had drifted away. Her illness seemed invisible to them. There were no visible signs, such as bruises, broken bones, or blood spouting from an artery.

After nearly two years, we decided the traditional medical community was not helping. Perhaps a naturopathic route could. We were told it was coming form an adrenal problem and were given vitamins, detoxifying footbaths, and massage therapy know as Reiki. All were complementary, but did not give her any long-term relief.

Time marched on. In April of 2009, we stumbled across the television show Mystery Diagnosis. This particular episode described Nina’s symptoms in remarkable detail. It was the first time I had ever heard the word Dysautonomia.

I immediately went to the internet to research this illness and people who could diagnose and treat it just in case that was what my daughter suffered from.

I found no specialists in the Pittsburgh area, so called every specialist within the United States. I then 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

Dr. Hassan Abdallah at The Children’s Heart Institute in Reston, Virginia finally diagnosed Nina with Dysautonomia.  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.

In addition to her prescribed medications, Nina 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), insulin resistance, and small intestinal bacterial overgrowth (SIBO). She also takes multiple vitamins and natural supplements daily to promote a homeostasis in her body. Her medication routine starts at 7am, continues every three hours, for a total of four prescription medications (14 pills daily), and seven natural supplements (11 pills daily)…

She combats all this by pushing herself to exercise with a trainer who specializes in strength and heart rate monitoring.

Last December, Nina had a procedure performed by Dr. Michael Arata called Transvascular Autonomic Modulation. It is much like angioplasty, but investigates the veins instead of arteries.

It is believed that by looking for venous compression and inflating a balloon at the superior portion of the jugular vein, one will reset the autonomic nervous system. It has proven successful, but turning back the clock of a chronic illness takes time and a lot of life style changes. Nina is still a work in progress.

Seven Years of Post Gardasil Nightmare

Nina was on the homebound 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 and 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, integrity, and relentless desire to live her dreams inspire 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.

Questions I have about Gardasil

I have researched Gardasil for a long time and still have these questions:

  • Why was Gardasil developed when 90% of all HPV infections clear on their own, without symptoms?
  • Why would the FDA place a vaccine on their fast track program (which means it only requires six months of research) if this vaccine was being administered to little girls?
  • Why was fast-track approval granted when an already safe and proven effective means of controlling cervical cancer is available in the United States?
  • Why do government health officials constantly ignore the facts posted on websites such as SaneVax Inc.?
  • Do medical professionals truly believe all of the girls with new medical conditions after Gardasil are just complainers and really don’t want to have a normal life?

Lessons We Learned From Gardasil

Gardasil taught our family 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.

Never judge a person with an invisible illness. Everybody carries some type of a burden in his or her life.

We are better people because of this illness. We no longer take life for granted. Lastly and most important, we trust God has a plan and we will continue the battle until his will be done.

This article in it’s entirety, is compliments of www.SaneVax.org

Francine, and Nina, I am so impressed with the fortitude, and faith you both carry.  Thank you, thank you for sharing your light, and story,  This will undoubtedly help many other girls, and their families. 

I am so glad that you have found SaneVax as well.  They have a wealth of information, including health practitioners with experience treating the effects of Gardasil/Cervarix.

Here is a little musical gift.  I hope you enjoy, and all the best!  jen

 

Cervarix survivors in the Czech Republic#HPV#Vaccines#Android