Gardasil: Ashlie’s Near-Death Experience#Mandated Vaccines#HPV Vaccine#World

February 19, 2014June 28, 2014 jlvranes Leave a comment

Shawna Snyder, Big Bear City, California

Ashlie before Gardasil

Who would have ever thought a single injection of the HPV vaccine, Gardasil, could bring my precious daughter to the brink of death? My daughters, Ashlie and Lyndsie, were both injected with the Gardasil on the same day. Lyndsie had no adverse reaction. Ashlie was not so lucky.

Ashlie has always been bigger than life. A girl who we know can handle anything. At the age of 4, Ashlie decided she wanted to dance. She was shy and didn’t like people staring at her, so we knew that this little endeavor would be short lived. We could not have been more wrong. As Ashlie became older, we knew she had found her passion and career in life. She was going to be a professional dancer and she was on her way.

How could we have known one vaccine would change our lives and her life so drastically?

In the middle of June 2009, Ashlie received her first and only Gardasil vaccine. Ashlie’s older sister Lyndsie was also vaccinated with Gardasil on the same day and had no adverse reaction. For that I am thankful.

However, approximately 16 days later Ashlie began to complain that her legs were not working correctly. Looking back, I am not sure what I thought it was, but I had her take some Tylenol. The next morning, I came downstairs and Ashlie was lying on the couch watching TV. She told me that she had crawled from her room and down the stairs to get to the couch. She informed me she could not walk. I asked her to stand. She tried and fell to the floor.

She was quickly taken to our local ER. The doctor threw his hands in the air saying he had no idea and it must be growing pains. She was given crutches and a prescription for steroids. I took her home convinced the doctor was wrong, as I am a mother of 5 daughters and had never witnessed growing pains like that.

Ashlie had been diagnosed with epilepsy when she was 10-years-old. I thought she perhaps had had a new seizure I was not aware of, so I called her neurologist. I was assured it was not a seizure, but to bring her to the ER (a different ER) in the morning as they were very crowded and she would be seen faster in the morning and we would get home quickly.

Later that night, I helped Ashlie in and out of the bathtub because she could no longer walk. I went to hand her something and to my horror discovered that her arms and hands were not working either. She literally could not pick up what I was handing her.

After a few phone calls, I rushed Ashlie to an ER over an hour away, the same ER we were to visit in the morning. I carried her in, and for a crowded ER on a Saturday night, she was seen within 1 hour.

One of the phone calls I had made was to my dad. His friend is a doctor, who told my dad that I needed to ask if it was “ascending paralysis”. While we were with the doctor, I asked him if it was “ascending paralysis” and he said yes. It appeared she had Guillain-Barre’ Syndrome (GBS).

I was asked if she had been sick and I informed them she had not. I could not figure out how she got this.

She was kept in the ER until a room became available in the “step-down” unit or intermediate ICU. At this point I still had no idea how serious this was. Once she was admitted to the hospital and not an ER patient, they handed me a bunch of literature on GBS. My answer to how she contracted GBS was in the first sentence that I read, and it said that you can get GBS from a vaccine. She had just had a vaccine, the Gardasil vaccine earlier that month.

Ashlie after one injection of Gardasil

As Ashlie lay in the hospital bed I watched her go from a vibrant young girl to a shell of non-existence. She was unable to walk, she was unable to get up to use the bathroom and as she couldn’t eat, an NG tube was placed in her nose so they could feed her. She was given intravenous immunoglobulins (IVIG), in the hope that this would stop the paralysis and start it descending.

She became delirious, and she began talking like a baby in her sleep. She was in extreme pain and I had no idea what to do, or even still did not realize at this point how serious GBS was.

Within 24 hours things went from bad to worse. Her respiratory system was shutting down. The GBS was paralyzing her to the point that she could not breathe.

She was rushed to the Pediatric Intensive Care Unit (PICU). Within minutes of being there she stopped breathing and they had to “bag” her. I could not believe what I was seeing. My baby girl was dying before my very eyes.

She could no longer talk and would finger spell (sign language) to communicate. They put her on a bi-pap machine to help her breathe and on July 1, 2009 Ashlie was intubated. She could no longer breathe on her own to keep alive, a machine had to do the work for her. Her heart was racing, ranging between 160-180 bpm. It seemed as though her heart would come through her chest. For the next 2 1/2 weeks, I sat and watched as she continued to get worse.

Guillain-Barre Syndrome is most common in older people, not children. It was the worst case the children’s hospital had seen in over 3 years. All treatments done to “reverse” GBS are done on adults. The hospital had to take adult treatments and alter them for a 12-year-old. She had more IVIG treatments done, she had plasmapheresis, MRI’s, and nerve tests done. The damage done to her nerves was horrific. The GBS not only destroyed her myelin, but it went into and began destroying the axon.

Slowly her body began to “heal” and the GBS started to descend. After 3 weeks of being intubated, she began to breathe on her own and was extubated. However, as the feeling came back, she was in excruciating pain. Pain so bad she felt like we were ripping her skin off if we touched her. We remained at the children’s hospital for another week. She was then transported to Orange County to Healthbridge Children’s Hospital for rehabilitation. Ashlie spent another 4-weeks away from home doing physical and occupational therapy 7-days a week. She was tired, her body hurt, her body would not cooperate at times, and we had lots of tears. After spending her 13th birthday in the hospital we decided it was time to go home and start our new lives.

Once at home Ashlie began physical and occupational therapy at home with an in-home health service. We tried to keep life as normal as possible for her. She started going back to dance class immediately, although participation was limited. She went to our local hospital for physical therapy.

After 6-months the therapists said there was not much more they could do for her and she was as good as she was going to get. That was not the answer I wanted to hear. She was only 13-years-old.

I began making phone calls and from there carried out more research. We were told to get her into Pilates with an instructor who had a dance background. We did just that and things started to fall into place.

Although some things fell into place, we noticed that Ashlie’s health began to change also. She was unable to keep foods down. Anytime she ate, she became very ill and everything came out one way or another. We noticed that she would have dizzy spells and pass out. She would have severe nerve pain at times, to the point that she could not be touched by anyone anywhere on her body. She said it felt as if her skin was being pulled from her body again. I have watched her go in and out of consciousness and struggle to breathe. She now has a rapid standing/sitting heart rate.

We have taken Ashlie to many different doctors and specialists. At one point they almost did heart surgery on her to try and stop her from passing out. She has been hooked up to heart monitors for 30 days and at the same time as this was happening, trying to continue to dance.

She has been seen in different emergency rooms over the last 4 years only to be told time and time again, that there is nothing wrong with her and that it is all in her head.

On the road to recovery

Finally, during the summer of 2013, I was reading a story about a girl who had been injured by the Gardasil vaccine. I never read the comments below because I find them to be rude or critical. This particular day, I decided to read one.

A lady mentioned a doctor who helped her niece. I contacted her and then the doctor. We saw him in Sept 2013 and started treatment in October 2013. It has been a long hard road. Ashlie has completely changed her eating pattern and takes many supplements. She has phone appointments with him every 4-6 weeks.

One of her goals was to become flexible again. A silly thing to most, but to her as a dancer it is everything. She is slowly but surely getting it back. I even watched her do a backbend from a standing position a few days ago. Something I thought I would never see again.

I regret every day giving her this vaccine, but I am so glad she is such a fighter and has not given up. Both mom and daughter are in this together and we will never give up. We hope too that whatever we can achieve for Ashlie can benefit so many other girls and boys who have also been badly injured by the Gardasil vaccine.

Mom and daughter, I am so inspired and amazed by your story. Thank you so much for sharing your struggles, strengths and all you have overcome. You have shown us what a process this journey has been and you have stuck it out well. It must be very difficult to share such personal things, but I know you do this so that other teens don’t experience this same trial.

Ashlie, you are such a fighter, and now beginning to dance again. What a triumphant story. I am so glad that you found a practitioner who is making a difference. I am sure there will be many more ups and downs, but I believe you will always gain a step ahead.

I chose this next artist because she relays the beauty and strength of woman so well and you two embody that same strength. Mom and Ashlie, thank you for the example of love and support you have shown to all of us. All our prayers go with you, jen 🙂

Jordan’s Journey from Gardasil into the Unknown#Mandated Vaccines#HPV Vaccine#Vaccine-induced Diseases

February 15, 2014June 28, 2014 jlvranes Leave a comment

What Gardasil did for Jordan

By Kami Wightman Fulton, Bitley Michigan

My daughter was an amazing athlete! Volleyball and wakeboarding were her life. Now, we are lucky if she can complete a full day at school let alone play sports. This all started a week after my daughter had the first shot of Gardasil and began to have lots of pain and swelling in her joints. Her knee in particular was really bad. It was terribly swollen as were her neck and ankles. The doctors thought she had Juvenile Rheumatoid Arthritis. After about a year, there has been no improvement in her condition, as a matter of fact it appears to be getting worse.
Now Jordan is experiencing stomach problems and feels very nauseous and does not feel like eating anything. She is also experiencing horrible chest pains and back pains. No matter how hard I try to make her feel better, there does not appear to be anything I can do which helps relieve her pain. To make matters worse, Jordan’s fingers turn blue, she gets a rash all over her body and her eyes always dry up, she suffers from shortness of breath and bad headaches.
The newest and most scary side effect is when Jordan passes out and has silent seizures. When these seizures started, she would have them once a month to twice a week but now she is having them every day and sometimes several in a day.
We have been to many hospitals but get no help. I find it difficult to understand that they cannot work out why these seizures are occurring and see how harmful they are to my daughter.
I find it very difficult to handle having to watch my baby girl go through this nightmare and there is nothing I can do to make it all better.
If she were having these problems because of a medication she was taking, she could simply stop taking it and gradually recover. It is really too bad she cannot be unvaccinated. I would give anything to be able to get the Gardasil vaccine completely out of her system.

Jordan, don’t lose hope. The magnitude of this trial only testifies to your strength. Fortunately, you have found the good folks at Sanevax. They have health practitioner contacts with expertise in this area. I do know, to an extent, the frustrations with searching for health answers. Lean on the Lord, and ask him to help you carry this burden. He knows exactly what your ailments are and can guide you to those who can help. It will probably be a process that will take longer than you or anyone else will want, but hang in there. If you continue to let your father in heaven guide you, I promise, you Will see miracles in your life.

So for now, kick your feet up, take a deep breath and enjoy some tunes.

sanevax.org

One of the reasons I love living in Utah#world#HPV vaccine#mandated vaccines

February 14, 2014June 28, 2014 jlvranes Leave a comment

I was reflecting today on how happy I am with our family move to Salt Lake City, Utah. There are plenty of reasons to like the state. The many National Parks, the beautiful mountain canyons, a friendly, healthy environment and so many family-friendly activities. I must say however, that I felt a certain sense of reverence with one particular thought.

Less than 42% of girls have received the full Gardasil vaccine schedule. From what I understand, that is the lowest rate in the county. That statistic alone deserves a Huge Huzzah!! I knew I was surrounded by so many caring, conscientious parents and friends.

There is something to be said for a parent that thinks things through, and doesn’t just follow blindly. A self-correcting individual.

There was a time when one could hold certain government offices in high regard, to know that our best interests were always on the forefront.

Unfortunately, those days are long gone with only the hope for a different day. One that employs less cronyism, revolving doors, money and prestige. Where the health and well-being of a nation is foremost.

I see today as a time to make thorough health choices in regards to our self and those in our care. A time of great healing for our vaccine wounded with a trump sounded to end the ongoing damage.

The One Thing Subway Is Still Hiding From All Of Us!#world#natural immunity#GMO’s

February 13, 2014June 28, 2014 jlvranes Leave a comment

I think Subway is a better fit in the food industry. — I think Subway is a better fit in the shoe industry.

Food Labels May be Inaccurate, Despite FDA Inspections

By Food Babe

Witnessing the power of the Food Babe Army this week has been absolutely incredible.

On Tuesday, February 4th, I launched a petition for the removal of a dangerous plastic chemical called azodicarbonamide from Subway sandwich bread – the same stuff used in yoga mats, shoe rubber and synthetic leather. This was after repeated attempts to reach out to Subway since June of 2012 to learn more about why they are using this (asthma inducing and potentially carcinogenic) chemical here in North America and not in any other countries. They never responded until now….Read the rest of the article here

I was so disappointed when I read this article but so grateful to be aware. I hope Subway gets there act together. This is not an oversight but outright choice in their administration. You wonder how these things get through our supposed F.D.A. watch dogs. Not the same anymore, is all I have to say.

“Food Babe” – A Woman on a Mission to Change the Food Industry, and How You Can Too

The Science of Vaccines#Pets#Pets and Vaccines#Vaccines

February 12, 2014June 28, 2014 jlvranes Leave a comment

Science of Vaccine Damage

Thank you Dr. Carley for the above material.

If you have a pet, this is a must read. Numerous valid points in regards to vaccination, pets and child alike. If you suffer from food allergies, you will find some vital information within the article. Nineteen, non-pharma scientists completed this research study.

The above article is worth it’s weight in gold.

www.reversingvaccineinduceddiseases.com

Cease Therapy #Autism Spectrum#MMR Vaccine#Mandated Vaccines

February 11, 2014June 28, 2014 jlvranes Leave a comment

Domenic Stanghini

Autism symptoms are increasing exponentially and the established medical thought is at a loss to explain or reverse this phenomenon. Our vulnerable children are the future for humankind and at this point it is looking bleak with 1 in 50 children being diagnosed as having ASD symptoms. ASD parents are spending everything they have to help recover their children with few positive results. Do NOT lose hope parents. There is something to help your ASD children when all else has failed. CEASE Therapy! And you will save thousands of dollars in the process when compared to other therapies.

CEASE stands for Complete Elimination of Autistic Spectrum Expression. It was developed by Dr. Tinus Smits from Holland and has its roots in Homeopathic Medicine. Dr. Tinus Smits wrote a book called Autism Beyond Despair. CEASE goes one step further than the natural Classical Homeopathic remedies that are suggested to recover Autistic children. It uses Isotherapy, which is a form of homeopathy, to detoxify anything in the human body that has become toxic. Each of us are different and what is toxic to one person or child may not be toxic to another. In some sensitive adults and children, vaccines, medications, or illness can become toxic. In other words the system can become overloaded and then any extra doses of the vaccine/medication can become toxic to the system. If this is continued over and over as is the case with vaccine/medications (or even salt etc.) then it becomes toxic to the body and the body has a hard time to remove it from the system and then stores it in the body. These stored toxins can become the source of ASD symptoms. CEASE therapy addresses the these toxins as the root cause. Once the root cause has been found and removed then the child can proceed forward and recover from Autism.

A simple explanation as to how our children are affected with ASD symptoms. Imagine you are in a physical fist fight with someone. You are fighting and they are fighting and no one is winning. At some point they gain the upper hand and land more blows. You are now in a weakened position with no ability to defend yourself. You continue trying to defend yourself but now the same amount of blows are doing damage to you whereas before they were doing minimal. As you continue with the fight you are incredibly weakened and the punches and kicks are increasing and NOW they are doing more damage as your ABILITY to defend yourself has been downgraded. What caused the inability to fight? Was it the first punch or kick? The 10^th punch or kick or the 50^th punch or kick? Hard to say but at some point it is observable that you are weakened and you were not the same. You lost the ability to defend yourself and any further blows to your physical body resulted in further damage to the physical body.

In some ASD children this is what is occurring! It may not have been the last illness, vaccine, or medication that caused the autism issue but this could be where the parents first noticed that their child regressed or changed. It could very well have been the 1 or 2 or 3 vaccines/medications or illness before that caused the regression. That regression could have been subtle. Like the 20^th punch or kick above, the vaccine or medication, caused a subtle regression but the body is now at the maximum limit to defend itself. Follow that up with a cold/flu etc and then another round of vaccines/medications and then the body regress’s further. But now it is really noticeable. This is where the parents eyes are wide open that harm has been done. That their child has changed and regressed. And yet going to their health care provider they are told to soldier on and give more medications and vaccines leading to further regression in the child. Therefore, it might not be where the parent notices the regression in the child that caused the regression but the illness, vaccine, or medication just before that that caused the issue.

Let me first say that not all vaccines or medications for children cause issues. In some cases it is needed and assists the child to grow healthy. In other cases it most definitely causes issues and there is a method to help the child recover, CEASE THERAPY. If you look at the above metaphor the child is the one who is defending itself in the fight really well. At some point the physical assault is not defended well and they are weakened. We could say that the blows and kicks that are not defended well could be any illness, any vaccines, any medication, any emotional issues, any thought issues that the child has that it can NOT process and then return to homeostasis. When that occurs the child is vulnerable. When a child is vulnerable and has a reduced ability to defend itself it is open to further attacks whether the intention is to help or hurt. The road to Hell is sometimes started with “positive intentions” Let me give an extremely typical scenario that any CEASE therapist has heard over and over in their practice.

Child is given their routine vaccines for 16 months and all is well and child is growing normally in all respects. They eat well, sleep well, eliminate well. Then the child gets a cold or cough and is feeling unwell. The next scheduled vaccine is given despite the illness, and the child cries lots with fever, pain etc. The parents give child Tylenol. Child gets worse. They then develop the flu and this leads to bronchitis. Antibiotics are given. This illness lasts for 6 months and now spreads to ear infection and more antibiotics are given. The next vaccine date is now upon the child and they are still not better and yet are given the next scheduled vaccine. The child has been dealing with illness for 12 months and 6 months ago the mother notices that their child is different. They are more different, talk less, more shrieking, mores stimming, more neurotic, more anger or apathy, talk is reduced, refuses to listen, anxiety and OCD increase, etc. etc. The mother was sure that it was after the last vaccine. And yet with this long list of illness the vaccine could have been that “last straw that broke the camels back”. These stories are very typical for the autistic community. As a CEASE practitioner we investigate and try to find the most causative agent that caused the turn downwards in health for the child. In this very typical case it could have been the multiple antibiotics or the vaccines or a combination of both. When the body is very low in immunity and is assaulted with more medications than it can handle it can become toxic to the system rather than help the system overcome the illness. Lots of medications can unbalance the homoeostasis of the GI Tract and then this upsets the delicate dance that goes on in our human ecosystem. This alone can contribute to ASD symptoms and many many ASD parents have seen their children have strange eating habits that have been very hard to change and this further leads to an unbalanced gut ecosystem and continued ASD symptoms.

It can also happen that giving the isotherapy of what the parents think caused the issue does nothing. In this case the CEASE trained homeopath will look to either what happened before this vaccine to further assist. Sometimes it is not that last vaccine/medication that caused the dam to break” but maybe was the vaccine/medication given before that.

With CEASE therapy we also use orthomolecular medicine. Basically we use 3 supplements and this will be a welcome change for some parents that have used upwards of 20-30 supplements and lots of $$$ for their child in hopes of recovering them. With CEASE therapy we use Omega 3 fatty acids to help with brain functions, high doses of vitamin C (fat and water soluble) to control inflammation, and zinc to aid with heavy metal removal.

If you are interested in their form of therapy for your child please go to CEASE Therapy and there you will get more information and find a practitioner in your area. Interview someone over the phone or skype and find someone that you feel comfortable working with. That is the most important thing. Find someone that willl listen to you, your child, your issues, someone that you can be completely honest to, and they will assist you to help recover your child from an Autism diagnosis.

www.dstanghini.com

dstanghini@gmail.com

647-500-4545

From a parent’s perspective – ilovequeenanneslace.com

Use Code SAVE10AX

Gardasil: The decision we will always regret#HPV Vaccine#Vaccines#Vaccine-induced injuries

February 10, 2014June 28, 2014 jlvranes Leave a comment

Gardasil: The decision we will always regret

February 4, 2014 By admin

By Kim Robinson, Red Hill, Pennsylvania

Katie’s Gardasil Experience

By all accounts, our daughter was normal before receiving the HPV vaccine. Katie performed very well in school. She was conscientious, hard-working and took pride in getting good grades. She loved dancing having taken dance classes since she was 3 years old. Katie always danced and twirled throughout our home and anywhere else she happened to be. When Katie was 10, she joined cheerleading and became involved in competition cheerleading. She was very active, taking four hours of dance class every week plus spending many more hours practicing with her competition cheer team. Katie was healthy and vibrant.

We were very diligent with our children’s health. We never missed an annual check-up and we also followed the pediatrician’s recommended vaccine schedule including annual flu shots. Our pediatrician recommended the Gardasil vaccine. The Gardasil vaccine was heavily advertised on TV. We read the vaccine Disclosure. It said that the vaccine should not be given to those with HIV. Katie did not have HIV so we signed the Consent.

On September 2, 2010 at the age of 11, Katie received the first Gardasil vaccine. Katie’s first day of middle school was September 7, 2010. Initially, we believed that her fatigue and headaches were being caused by having to get up much earlier in the morning for middle school. However, she never adjusted to the new schedule and soon her symptoms began exploding. Katie would often tell us “I don’t know what’s wrong, I just don’t feel good.” She began sleeping a lot – over 12 hours a day and even more on the weekends, which would allow her gather enough energy to go to school a few days before she crashed again. She missed days at school, dance lessons and cheer practices. Soon her illness was visible on the outside too. Katie didn’t look good – constant dark circles under her eyes, her skin color was ashen and she appeared listless.

To us, it seemed that her symptoms must be related to the Gardasil vaccine. Katie’s earliest symptoms began after receiving this vaccine. We searched the internet but only found vague information – nothing that matched our daughter’s symptoms. We asked Katie’s pediatrician and other specialists if the Gardasil vaccine could be related to her symptoms but our inquiries were quickly dismissed as not having any correlation to her illness. Katie’s earliest symptoms were a constant headache or migraine that did not respond to pain relievers, stabbing 24/7 bilateral ear pain, fatigue not relieved by sleep, abdominal pain, nausea and joint pain. We called and visited her pediatrician repeatedly. We began taking Katie to specialists including Neurologists, ENT’s, GI, and an OBGYN and made several visits to the Emergency Room. Katie also received many blood tests, CAT scans and an MRI. Nothing any of the doctors did relieved Katie’s symptoms. As a matter of fact, the drugs prescribed to alleviate her symptoms only made her feel worse. Our pediatrician and other doctors involved with Katie’s care began suggesting that her illness was psychosomatic and recommended that we take her to a psychologist. We soon found that we were on our own, dealing with a medical issue we did not understand but trying desperately to help our daughter.

When searching the internet with Katie’s symptoms, Lyme disease would always come up as the search result. In addition to asking all of Katie’s doctors if the Gardasil vaccine was the cause of Katie’s illness, we also began asking if Lyme disease could be the culprit. In October 2010, Katie was first tested for Lyme disease. The results were negative as were two later rounds of testing. We read on the internet that ELISA and Western Blot tests for Lyme disease are unreliable and that many people who actually had Lyme disease tested negative. Since this information is all over the internet, we thought it was common knowledge to doctors as well. Instead, we were emphatically told by doctor after doctor that this was not true, that the testing for Lyme disease is highly reliable and that there was no way Katie had Lyme disease. In April 2011, Katie could no longer go to school or participate in dance or cheerleading – the pain and fatigue was all consuming. Nothing any of the doctors did provided any relief yet every doctor refused to consider Lyme disease or that the Gardasil vaccine was related to her illness.

Katie’s list of symptoms included the following: 24/7 headaches and migraines, 24/7 stabbing ear pain, hyperacusis, fatigue, abdominal pain, nausea, all over joint pain, constant sore throat, visual disturbances, light sensitivity, cognitive issues such as memory and severe comprehension problems, random numbness and tingling, weird “bug crawling” skin sensations, generalized weakness throughout her body (it was difficult for Katie to just sit in the shower to bathe), dizziness, fainting and heart palpitations. She slept long hours and stayed in her bedroom shielding herself from the noise of everyday living.

In May, we requested testing through a lab specializing in tick-borne disease testing. Katie’s pediatrician reluctantly signed the lab Requisition Form. This time the test results showed that Katie was highly positive for Bartonella Henselae, a tick-borne disease also known as a co-infection to Lyme disease. She was also highly positive for Mycoplasma Pneumonia and the testing showed that her immune system was struggling. Katie’s Western Blot for Lyme disease was negative.

Katie: My Gardasil Nightmare

We took those results with us to a long awaited CHOP Diagnostic Center appointment (think the “Dr. House” of the Children’s Hospital) and also to her CHOP Neurologist. Katie even had the classic Bartonella rash (looks like purple and red stretch marks) surrounding her breasts and hips which is confirmation of an active Bartonella infection. Both doctors told us that these test results only showed that Katie was “exposed” to Bartonella – it did not mean she had an active infection. Both came to the same conclusion that her Bartonella rash was actually just stretch marks. That was particularly hard for us to believe. Katie was muscular and lean from years of dance and cheer.

Neither doctor was concerned about her blazing Mycoplasma Pneumonia infection nor was the fact that the testing showed her immune system impaired. Instead, CHOP Diagnostic Center diagnosed Katie with the beginning stages of Dysautonomia (a malfunctioning automatic nervous system). We were told that there was no cure and that symptoms were managed with medications. The CHOP Neurologist wasn’t in agreement with CHOP Diagnostic Center; instead she stuck to her prior diagnosis – Chronic Migraine Disorder with Chronic Ear Pain Neuralgia. The Neurologist recommended that we continue with the same treatment of 20 pills a day even though it did absolutely nothing for Katie other than increase her nausea and head pain. We felt utter disbelief, despair and anger.

We found our way to a local support group for those suffering with tick-borne diseases, which provided recommendations to LLMD’s (Lyme Literate Medical Doctors). Katie’s first appointment with an LLMD was in June 2011. This physician spent an hour reviewing blood tests and other medical reports we collected and asked a lot of questions that had never been asked before. He clinically diagnosed Katie with Lyme disease and agreed with the test results that reported active infections with Bartonella Henselae and Mycoplasma Pneumonia. He told us that Katie was very sick. Ironically, upon hearing that news we felt utter relief. This was the first doctor, since Katie’s illness began over nine months before that acknowledged she was ill. Since that time, Katie was diagnosed with chronic Strep, HHV6, hypo-coagulation, susceptibility to bio-toxin illness (mold and environmental sensitivities) and has acquired autoimmune thyroid disease.

It has been three and a half years since Katie received the Gardasil vaccine and she still remains chronically ill. She was unable to attend school in 7^th and 8^th grades. This year, Katie decided to repeat 8^th grade again rather than begin high school still sick. Katie has an IEP plan in school which reduces her daily schedule to three core classes only. Unfortunately, Katie is still too sick to attend school with any regularity. Most days, a teacher comes to our home to review the lessons she missed at school. Some days, Katie’s pain levels are too high so that she can’t even tolerate home tutoring. Although she longs to get back to dancing again, she spends most days in her room sleeping or resting and trying to cope with chronic pain. At 14 years old, Katie’s life closely resembles a sick elderly person instead of an active vibrant teenager she should be.

After Katie was finally diagnosed with tick-borne diseases, we put our initial suspicion about the Gardasil vaccine aside. Since the treatment of tick-borne diseases is considered emerging medicine, I am always combing the internet for new information on tick-borne diseases, the latest research or treatments. To our utter disbelief, I came across an article reporting that the Gardasil vaccine can activate a latent Bartonella infection that was otherwise being suppressed by a properly functioning immune system prior to vaccination. We now believe our earliest suspicion was correct.

We found many stories about devastating health changes post-vaccine. These stories are eerily familiar to our daughter’s. The Gardasil vaccine is known to activate latent infections and viruses, such as Epstein Barr and Bartonella. The Gardasil vaccine deregulates the immune system and that allows latent infections and viruses, which were kept in check pre-vaccine by a then properly functioning immune system, to activate post-vaccine. Now, there is evidence that the HPV vaccine is linked to the onset of autoimmune diseases.

We recently consulted Katie’s LLMD and also her Primary Care Physician, who reviewed Katie’s vaccine log and extensive medical records. Both agree that Katie’s immune system was injured by the Gardasil vaccine and that it was the catalyst to her cascading health problems and chronic illness. Katie’s LLMD is now treating her for a vaccine injury in addition to treating multiple tick-borne diseases, other infections/viruses and autoimmune thyroid disease.

At this point, we are totally outside our insurance company and most everything is out-of-pocket. The overall expense of Katie’s illness greatly outpaces our income so many expenses are put on credit cards. But the biggest cost by far is the toll that the Gardasil vaccine has taken on our daughter’s health and well-being. We wonder if she will ever be able to reclaim her health and get back to living a normal life free of pain.

We deeply regret consenting to the Gardasil vaccine. We had no idea of the severe side effects some experience post vaccine. Every day, we wish we had been more informed. Parents beware of blindly following your doctor’s recommended vaccine schedule. Do not rely or expect your doctor to know everything. You must do your own research and ask plenty of questions. Our family found out the hard way that it is possible for a vaccine to have lasting and devastating effects.

Article complements of sanevax.org.

Katie,

I can only imagine the grief and pain you are enduring. Thank heavens for your supportive and dedicated family.

I think that with difficult circumstances and trials, that are unique to this era, our father in heaven provides

blessings of healing and health that are unique to this time as well.

Continue to keep Him in your prayers and don’t lose hope.

You are a strong and talented girl, and none of that has changed.

Thank you , for sharing your story. We all have much to learn from you and your family’s journey.

I have a special, little gift for you. I hope it can help take your mind off things for awhile.

Our hats are off to you, from cheerleaders all over.

Your friend,

jen 🙂

BOMBSHELL TV SHOW ABOUT HPV VACCINES REVEALS CRUEL NATURE OF VACCINE PUSHERS#HPV Vaccines#Autism Spectrum#Vaccines

January 31, 2014June 28, 2014 jlvranes Leave a comment

Vactruth.com

Sandy Lunoe

Refreshingly, there was a brave attempt recently in a popular show seen by over two million viewers on ABC TV1 to present balanced information regarding the controversial HPV (human papillomavirus) vaccines.

(1) It was expected that to touch on the subject of vaccine injuries and death would bring down the wrath of the vaccine industry. And it certainly appeared to do so.

In addition to opinions from vaccine promoters there were interviews with a grieving mother who shared the tragic story of her daughter’s death and a brave young girl who described her suffering after the vaccine. Two doctors gave their opinions. Whilst one was in favor of the vaccine the other questioned its necessity given the overall success of Pap testing to screen for cervical cancer…

Bombshell TV Show About HPV Vaccines Reveals Cruel Nature of Vaccine Pushers

Click on the link above to read the entire article.

Words cannot express the sympathy and love I feel towards the many families hit hard by vaccine injuries. I was hesitant to post the above article due to the hateful comments towards these families. I am almost speechless by this prejudice and only wish to say, “By their fruits ye shall know them”.