Comment from Vaccine-Injured Archives - Page 2 of 7

Gardasil: Don’t let your child become “One Less”#MTV#teen#Android

March 11, 2015March 10, 2015 jlvranes Leave a comment

By Shannon Powers, Ohio

Our healthy active funny daughter became just that! I share our story hoping our experience will save another from becoming “one less” healthy child.

Our fifteen year old daughter, Leah is vaccine injured. It all began March 30th 2011. Leah was 11 years old, soon to be 12. We had been referred to an Adolescent doctor so Leah could be placed on oral contraceptives to help prevent cysts from forming on her ovaries.

A month prior, February 20, 2011 Leah had an Oophorectomy losing her left ovary. We were told since we had just gone through this scary ordeal, in order to keep her healthy we needed to vaccinate with the Gardasil vaccine.

Trusting in doctors and believing what they recommend is best, I never questioned their belief that this was a “must” for Leah’s health. After all, Leah had received all her recommended vaccines prior to Gardasil. What could we possibly have to worry about?

First, I have to tell you Leah has a very high tolerance for pain. The only way I knew I needed to take her to the hospital in February was because she was clammy and dry heaving. The surgeon who performed the Oophorectomy came and told us after, that she should have been in excruciating pain.

She laughed when telling Leah, “I tells my kids to quit complaining all the time, but YOU need to complain and let us know when something is wrong in your body. You know your body best and when something is off let mom and dad know!”

Recovery went smooth and we then were released and referred to the adolescent doctor for all of Leah’s follow-up care.

March 30, Leah received the first shot in the Gardasil series from Lot number #1437z. After we left the paediatrician’s office Leah said she felt sick to her stomach. I thought due to being only 4 weeks post-op she was going to feel a little ill from the car ride. But, by the time we got home she was nauseous and bloated.

I called the doctor and was told it all stemmed back to the surgery. They had removed her left ovary, so she probably was having effects from the anaesthesia that was used during the surgery. We didn’t question the response and left it at that.

The following four months she continued to have severe abdominal pain, bloating, nausea and feeling full after just a few bites of food. I called again during this time and was told because of the removal of the left ovary she was just feeling her body adjust to what her insides were adapting to with more room. They assured me it was normal and there was no cause for concern.

August 8, 2011, Leah received her second Gardasil shot from lot number 1271z. We didn’t mention anything about her new medical conditions during this visit because they had already given an explanation over the phone to why she was experiencing these symptoms.

For the next four months Leah’s symptoms did not improve. Every time she ate she felt sick. She was always nauseous and her stomach was extremely bloated. I start researching her symptoms and then became worried it might be ovarian cancer. All of her new symptoms pointed in that direction. Never once did I feel it was the vaccine. Doctors were all guiding me back to the Oophorectomy.

December 12, 2011, Leah receives the third and final dose of the HPV vaccine series from Lot# 1261AA. By this appointment I was very concerned with Leah’s health. She had continued to have the severe abdominal pain, bloating, nausea, feeling full, headaches came and went, and she was not sleeping well.

In order to appease me, doctors told me they would do a cat scan to make sure her right ovary was all right. I asked them to do a blood test, CA125. This would measure the protein in the blood, detecting early signs of ovarian cancer. I was told that it would come back positive because she had just had the Oophorectomy. So it would not be accurate to do the testing.

I will be honest, I hadn’t researched to see how long it would take from the time of the surgery for her to keep testing positive, if it would at all? I did keep questioning them. Again, I trusted them and thought they knew best. After all, they have the degree, I don’t…..right??

Cat scan came back normal. Everything looked fine. We were told to hydrate and make sure she was moving her bowels. They changed the oral contraceptives thinking that would help relieve some of the symptoms.

All of 2012 Leah continued with the same symptoms. I kept telling her to push through because they said nothing was wrong. She is constantly coming to me with aches and pains, here and there…arms will hurt, legs hurt, feels funny. I ask my husband if we have made her a complainer since the surgery. I tell Leah she doesn’t have to tell me every time she hurts somewhere.

Looking back on this now, breaks my heart to think I ignored a lot of symptoms she was actually having. Like I said before, her pain tolerance is high, she wasn’t physically showing how bad the pain was or crying in pain, it was more of “matter of fact” so, I played it down instead of really listening.

The end of 2012 I take Leah to an actual OB/GYN. She had never stopped complaining with all of the symptoms from the last year. I was still scared and thinking it was Ovarian Cancer. This new doctor spoke with Leah and me and said she would order an MRI and double check that everything was okay. Leah to this date has never had an actual Pap screening concerning her cervix or uterus. MRI was normal and this doctor put her on yet another new contraceptive. Said a low oestrogen would help with the pain and the headaches.

During this whole time since her Oophorectomy, Leah has never had a normal cycle. She would bleed for maybe a day and it was always black blood. Of course they say this is normal and all due to the contraceptives; always assuring me that everything is fine.

The whole year of 2013 Leah continues to just push through the pain. The doctors say make sure she is hydrated, that her bowels move, it’s the contraceptives or normal teenage hormones. Her medication is changed several times trying to see if that would improve symptoms. It never did.

By the end of 2013 Leah is complaining about her vision. She does wear prescription glasses/contacts so I made an appointment to have her eyes checked out.

Before I tell the rest, I have forgotten to tell you about who Leah truly is… Leah is an honor roll student. She loves to read and write stories. She will finish a book in just under a day. She was active in 4H and loved taking animals to our county fair. She has taken pigs, rabbits and goats as well as creative writing. Excels in her studies and plays various sports.

You will laugh in her presence when you don’t feel like it because she will do or say something silly to change your mood. She is very outgoing and always makes friends wherever she goes. She is always laughing and singing 80’s music.

The year of 2011/12 she was playing with the local YMCA club volleyball, basketball and softball for her middle school along with travel softball in the summer. She continued with the softball for the school and the travel ball throughout the next two and half years. Softball is her favourite!!

She was excited for the summer of 2014. It was to be a great summer before becoming a sophomore in high school. Players were starting to write to different colleges that they would be interested in attending and possibly to play softball for. They would write to the head coaches and explain they were interested in playing for them while attending their college. Asking for them to come and watch them play for their travel ball teams, in hope of gaining their respect by wanting them to represent their school. Hoping they would keep in touch during the rest of their high school years.

When your academic scores are high and you play ball well enough, colleges are pleased to offer scholarships. Leah was taking this very seriously. One of the colleges Leah wrote to, Rhodes in TN, came to Ohio and watched her play. She was ecstatic and that just made her want to strive harder. She pushed through last summer playing in more pain than before, but worth the pain for the sheer joy of a sport she loves and was wanting to continue playing through college.

We are now in the beginning of 2014. It is January and her vision had changed so we order new contacts and glasses. The Optometrist never questioned anything out of the norm when examining Leah. Wrote a new script and we were on our way.

Leah’s headaches were increasing and not leaving her at all. She is still suffering from the severe abdominal pain, bloating, feeling full, and nausea. She was now having blurred vision even with her new script. Doctors were saying the contraceptives will cause eye issues. Nothing they could do.

She starts having bladder spasms and feels like she always has a bladder infection. When doctors sample her urine we are told just traces of white blood count and that she doesn’t have an infection.

Sharp shooting pains down through her groin. Her right hip is always hurting. We are told over and over to make sure she hydrates!

It is February and she is conditioning for softball. She is having difficulty keeping up. Feeling as though she wants to pass out. Not able to keep her breaths regulated. Of course we are told she needs to hydrate and she had taken the winter off so she was out of shape.

This continues the rest of the school year. She keeps pushing through just so she can play ball. School is over end of May. Travel ball conditioning starts up. Her headaches are more severe along with all the other symptoms. She is experiencing all over pain that won’t go away. She sleeps the day away until it is almost time to go to ball practice. She practices two to three times a week and plays all day on the weekends.

I have noticed that she sits more when not playing. She will come and sit with me, not wanting to join in with the others. Not just at ball but when we are out as well, she will not leave my side. She starts acting like she is afraid to do anything by herself.

Headaches get so severe we go to the ER. Right away they see that her optic nerves are swollen. They call in an Ophthalmologist and he confirms what they see. They do a CT on her head, it shows normal so they ask us to come into the office the next day for more abrasive testing. Next day all tests come back fine.

They tell us to give it a month and come back for recheck. If they are still swollen but no change in tests then it is a birth defect.

THIS is when I finally wake up! How can it be a birth defect if the eye doctor didn’t see it back in the beginning of the year? Or when we were at the doctors for bladder pain?? Doctors always check your eyes, wouldn’t they had seen it then?

I was ignored and asked to schedule for a month out. Meanwhile, we were referred to a Headache clinic.

This Clinic acknowledged what other doctors saw and said her headaches were more than likely genetic headaches. Take some pain reliever and rest, along with drink more water!!

Even with Leah’s pain she still pushed through. She wouldn’t take any type of pain reliever. Said it didn’t help, so why take it? She hides the pain well, so I would just try and make sure she was staying hydrated.

Ball season comes to an end…School will be starting in a week. She is sleeping more. Emotions are all over. She acts like she is still afraid of everything. She won’t even walk by herself from the car to a friend’s front door. Wants me to walk with her??? Wherever I am she wants to be. Not wanting me to leave her side. She is becoming anxious, having lucid dreams. Trouble sleeping, pain is all over her body. She is waking up drenched in sweat. Cold and hot throughout the day. She feels as though her body cannot support her own weight. Tremors in her arms legs and face. Her hands and feet keep going numb. She was having low grade fevers and all the symptoms she has had for the last three years have increased.

She is changing from once a healthy girl to one that can’t even get out of bed. It is August 2014, her sophomore year starts and she is excited. She is planning on getting her temps in October, attending homecoming and playing fall travel ball.

Leah comes home from school exhausted. She falls asleep right away and wakes up in more pain than before. She says she is hurting so bad at school she has a hard time concentrating and understanding what the teachers are saying. She’s having a hard time hiding the pain from her friends. As she walks to each class she says she feels as though she is going to pass out. She’s still having severe back pain and new pains going down into legs. Lights hurt her eyes while inside and when she steps outside the pain shoots through her head making it difficult to see. Lights are too bright all over. The sun is torture. Her legs are having more spasms and her heart keeps racing even when sitting still. She started to just stare off into space and writing words over and over in her school work like she is stuttering, not realizing this until she reads her work.

Research came to my attention about the Gardasil vaccine and adverse reactions. When Leah came home from school one day I asked her to please write everything down, all her pains and odd things that was happening with her body. I told her I believed it was all happening because of this shot.

I made an appointment with her pediatrician and started to research. The more I researched I was certain this was what was happening.

When we saw the doctor she didn’t think that was the case. I told her there was a lot of research out there and how was it that Leah’s symptoms were the same as what was happening to all the other children claiming it was the vaccine as well??? The only common factor was the GARDASIL.

She listened and because of all of Leah’s symptoms she referred us on to several specialists. She ordered what blood work she was able to do. Said she would look into it and would be in touch.

I requested the lot numbers from her adolescent doctor and checked them from a study I found on SaneVax. Dr. Lee had done a study back in 2012 and found several lots to be contaminated with a non B conformation DNA attached to the aluminium adjuvant.

I wasn’t sure what all that meant, but reading through all the information I could find, I started seeing that this shot was sheer poison. When I checked Leah’s lots against what Dr Lee had tested I started to cry. There in black and white was the very first lot number that Dr Lee had tested-the same lot Leah had been injected with!

I was sick. I was mad. Then I realized I had Proof!

As I continued my search for the truth about this vaccine, I was discovering that thousands among thousands all over the world were injured the same as my daughter. Some far worse than her. None that I had found had one of the lot numbers in the study. That told me that EVERY LOT of this senseless vaccine could have the same contaminates as the one in the study!

We have been to eleven different specialists. Most of the tests all come back normal. A few have discovered some type of medical disorder. I have to say that I guess I wanted to rule out any major diagnosis. Doctors are quick to get you out of their office once you mention the possibility of vaccine injury. We are left feeling our only hope is a Bio Medical doctor that does not treat from a pharmaceutical manual. I have lost all trust and respect for any doctor that treats and diagnoses their patients from those manuals.

We were not treated with respect and care. We were told there was no way the Gardasil vaccine could be the reason for all of Leah’s new symptoms. Some even questioned why we would even consider a biomedical doctor. Most found it hard to believe Leah was having all of these symptoms at the same time. Several referred us to a psychiatrist!

I had a phone conversation with one of the psychologists, let’s just say once I started describing what was happening to my daughter and how I had PROOF, they were NOT going to diagnose her with Conversion disorder!

Our conversation ended with, “I am so sorry you and your daughter are going through all of this. My services are not needed at this time. If you feel like you would need for Leah to ever talk to someone, please let us know!”

WOW!!! Thanks doctor for the wonderful concern!

My daughter IS VACCINE INJURED from the HPV vaccine GARDASIL. She has been diagnosed with Lyme disease, metabolic disorder, immune deficiency, and encephalopathy, chronic gastritis with pre-cancerous cells throughout her stomach and colon, and ovarian failure.

She has several ACTIVE viruses within her system which include; Bartonella, babesia, coxsackie B, francisella tularensis, and HPV-6. The HPV-6 was a strain that this senseless vaccine was to fight against!!!

She is heavily toxin with heavy metals that do not want to leave her body. We are receiving treatment and trying to detox her body. Hopefully one day soon Leah will be her Healthy, Active, Funny self.

I urge you if you have not yet received the vaccine, DONT!!! DON’T LET YOUR CHILD Become “ONE LESS” HEALTHY ACTIVE TEENAGER!

Research for yourself and look at the prescribing information that comes with each vaccine. I promise you, if you do you will never vaccinate your loved ones again, with any vaccine!

If you are injured as well from this horrific vaccine, I am truly sorry! You have found HOPE by finding this site.

I promise to ALL of you that are injured, I WILL NOT STOP FIGHTING TO GET THE WORD OUT! I will go to whatever lengths I must to prove to the WORLD what is happening to our children is unethical and needs to STOP!!

Blessings to all!

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

Shannon and Leah, it was hard to read through the piled on adversity you have been through. You are strong women, and have endured this time amazingly well.

I am so glad you have located SaneVax, they are angels, and have expertise in healing from vaccine injuries.

I have a Featured Doctors menu option as well, with doctors that have experience in this area. I hope the tide has turned and things only improve for you from here.

I chose the following artistic piece for you being it hits on the depth of pain you must endure at times, and the reminder that, “Whoever saves one life saves the world entire.” A great man was given a gold ring with that phrase engraved on the inside for his generous, and courageous acts as seen in the film, “Schindler’s List”.

For you to take the time, with all you face each day, to reach out, and to save other teens from the tragedy of the Gardasil/Cervarix vaccines is touching. I am certain that you will save another in this effort.

I hope your testimonies travel far, and that Leah, you receive all the care that you need.

You will be stronger from this, and I believe you can receive miracles in many different ways.

Being that you are putting your trust in God, you will never be alone and he will guide your every step. God bless, your friend, jen.

Cervarix: Will my life ever be normal again?#Android#iBelieve#iPad

March 2, 2015February 28, 2015 jlvranes Leave a comment

By Saskia from Devon, UK

Cervarix changed my life: now I would never be able to manage the sort of day I took in my stride as a thirteen year old. I can’t even remember what a day with energy feels like.

Before receiving the HPV vaccine at 14, I was an active, mostly healthy child. As we lived some distance away from my school, I had fairly long days: I would leave the house at 7.30 am and return at 5.30 pm, but always came back with lots of energy. I enjoyed walking, swimming, horseback riding etc. after school. No matter how long my day was, I certainly never experienced the complete exhaustion I felt after the Cervarix vaccine.

The difference in energy was particularly noticeable because it happened immediately. The day I got the first HPV vaccination Cervarix, on the 28^th September 2009, I came home feeling sick and incredibly tired and had to go straight to bed. The next day at school was a struggle because I felt nauseous and so low on energy, and once again I ‘crashed’ when I got home and had to go straight to sleep.

This happened every day for a week or so. My mum rang up the local health service to talk to them, but they said this wasn’t a possible side effect of the vaccine and there was no way of registering any side effects.

Eventually mum managed to get through to a central line where she could register the nausea and fatigue I was experiencing. They also told her it wasn’t a known side effect of Cervarix and claimed there was no connection.

The same symptoms happened after the other two injections of Cervarix (on 13^th November 2009 and 24^th April 2010) but each time it got worse. After the second vaccination I experienced the same sickness and exhaustion but it lasted for a fortnight.

After the third vaccination I honestly don’t think life was ever really ‘normal’ again. The fatigue became more and more constant. I struggled with low energy levels at school, would fall asleep at lunchtime and on the way home and often had to go to bed as soon as I got back.

The constant exhaustion became very limiting. I had to stop swimming which I had done at a competitive level and greatly enjoyed. I also had to turn down a World Challenge Trip to Kenya despite having started fundraising because I realized I simply would not have the energy to walk each day. My fatigue now is sometimes completely debilitating and I spend much of my time in bed. I have become used to having to turn opportunities down because of it.

Not long after the third injection, the chest pain started. The first time it happened I was in a class at school and suddenly got a crushing pressure and pain on my left side. I felt faint and dizzy and was in so much pain I could barely talk.

I ended up going to a local A&E where they did an ECG and found that I had a very fast and slightly abnormal heart-rate accompanying the pain and so I was transferred by ambulance to Torbay Hospital. The pain eventually subsided and further ECGs came back normal and so I was discharged.

This was the start of an incredibly scary and difficult journey to getting diagnosed. I have experienced debilitating, severe and intermittent chest pain ever since. It has taken years and lots of time and energy to get a diagnosis.

The sickness and nausea is also something which started with the vaccine and has never really gone away. I spend most of the day feeling very queasy, sometimes to the point that I cannot eat anything. Despite trying many different anti-nausea medicines, I have yet to find one that works. I also started getting dizzy and fainting, particularly on standing or exertion, which has been very unpleasant and scary. Recently, my fainting has become significantly worse and now happens almost daily which is frightening and dangerous, and has led to several concussions.

Along with the horrible, debilitating symptoms of fatigue, nausea, chest pain, dizziness, fainting and gastrointestinal issues which are all linked, has come the struggle to get a diagnosis and adequate medical support.

I have been in and out of doctors’ appointments and hospitals since I was thirteen. There have been countless blood tests, ECGs and scans. Both my parents and I have had to spend so much time and energy researching and pushing for some help.

Despite the severity of my symptoms, they were initially dismissed as anxiety, then food intolerances, and later, because nothing was structurally wrong with my heart, the medical support became virtually non-existent and I was even told it was all in my head. One example of this treatment is when I went to a GP to ask for something to help with my frequent vomiting and was instead given the name of a book about ‘psychosomatic illness’. I can’t begin to describe how painful that is.

It was 4 years after my symptoms had started that I was finally put on a week-long heart monitor. This monitor picked up severe spikes in my heart rate. It showed times when my heart rate was quickly accelerating from 70 bpm to 180 bpm. These ‘spikes’ coincided with when I was experiencing chest pain or fainting. I was given a probable diagnosis of Postural Orthostatic Tachycardia Syndrome (POTS) which has since been confirmed by a specialist in Derriford Hospital following further testing.

I am now nineteen years old and despite finally being on various medication to help manage my symptoms, I am severely limited by my ill-health. I have no energy and often had to miss lectures, supervisions, social events and various opportunities because I am either too fatigued, too faint, or in too much pain to participate. Recently my ill-health has forced me into the incredibly difficult decision to drop out of my second year at Cambridge University, because studying has become impossible.

I have gone from enjoying exercise and loving long walks on the moors to sometimes fainting after a short flight of stairs, being reliant on taxis, and having to spend much of my time in bed.

I have gone from being a normal teenager to a disabled one, and it seems to have all been triggered by the vaccine.

Since the Cervarix injections and since developing POTS I have lost count of how many times I have been in hospital, experienced severe chest pain, fainted, missed important opportunities, and been sick.

In fact, I have actually forgotten what having a healthy day feels like as I am never symptom-free anymore.

This article in its entirety is compliments of www.sanevax.org

Saskia, I am so sorry you are going through this painful time. It is a shame that the medical establishment has let you down in so many ways and the psychosomatic illness suggestion just adds insult to injury. Just a lazy, weak cop-out. It is so much more pleasant when a doctor just admits when they do not know what is wrong.

I have good news for you, there are doctors that are experienced in this area, and will take you under their wing. Distance is not an issue in most instances. The team at SaneVax Inc. has wonderful contacts, and I have some as well within the Featured Doctors menu option on my blog. There are many others that have received relief and healing from Cervarix and Gardasil injuries.

I hope you are soon to be able to receive better care and to resume your studies at Cambridge University.

You can tell you are strong and patient, and I know that as you remember who you are, that you will continue to be guided on this healing path.

Here is a musical gift that I hope lifts your spirits at this time. My ten year-old daughter was watching me work and I asked her which musical group I should pick a song from. She felt this would be a good group. Hang in there, your friend jen.

The Gary Null Show – 02.19.15#Android#iPad#masterchefit#mommywithstyle

February 27, 2015March 1, 2015 jlvranes Leave a comment

This is a must listen to podcast. Good to play in the background while you are working or driving. Gain clarity and insight that you won’t find elsewhere in regards to, thirmerasol, the toxic mercury ingredient found in many vaccines.

Dr. Flannery, one of our, Featured Doctors, is also interviewed in this podcast. Hear what he has to say about his experience with treating vaccine injuries.

Documentary – Trace Amounts – on history of thimerosal and the government government’s coverup on its relationship to autism

– Eric Gladen is the director of the recently released documentary Trace Amounts – a film 10 years in the making that deeply explores the many scientific and politicized medical controversies associated with the relationship between the mercury compound thimerosal found in vaccines and the epidemic rise in autism and other neurological disorders. In 2004, after receiving a tetanus shot containing thimerosal, Eric’s life completely changed with the onset of a cascade of adverse physical, neurological and mental symptoms following the vaccine. For the next decade, Eric researched the autism’s “causes” associated with vaccine ingredients and traveled the country to interview and film scientists and individuals questioning the safety of vaccine ingredients to produce this documentary. Eric has an engineering degree from Oregon State University and his website is TraceAmounts.com

The science behind thimerosal and autism

– David Geier is the Vice-President of the non-profit Institute of Chronic Illnesses, Inc and the Vice-President of the non-profit Coalition for Mercury-free Drugs. He has extensive experience as a medical research scientist and has co-authored over 100 peer-reviewed scientific/medical journal articles, book chapters, and other publications. Fifty of his studies examined the safety of such vaccines as hepatitis B, DPT, HPV, the MMR, Lymes, Hib, and polio. An additional 25 studies investigated the safety of the mercury compound Thimerosal. In recognition of his scientific research, David has been invited to present at numerous professional conferences around the world, including giving presentations to the Institute of Medicine of the US National Academy of Sciences. His scientific research includes the study of vaccine safety, autism and other childhood neurodevelopmental disorders, toxicology, and molecular biological mechanisms. David is a biology graduate of UMBC and also studied vaccine science, immunology and epidemiology at the NIH’s Foundation for Advanced Education in the Sciences. His website is MercuryFreeBaby.org

Continue to the site here

http://thegarynullshow.podbean.com/

Gardasil: I thought I did enough research – I was wrong#Family#Android#iPad

February 19, 2015February 18, 2015 jlvranes Leave a comment

By Karen, County Louth, Republic of Ireland

My daughter Laura has just turned 17 and is without doubt another girl whose life is ruined as a result of the HPV vaccine Gardasil.

When Laura first brought home the consent form from school in 2010 I read it thoroughly. I also went on the World Health Organisation (WHO) website to educate myself about this vaccine as it was new here in Ireland and I didn’t know much about it.

After reading their information and that supplied by our Health Services, I felt not only reassured that this was a safe vaccine but also that this was something very important for ‘my little girl’ and her future health. I stupidly thought that all details good and bad had to be printed so parents and girls could make properly informed choices.

Let’s not forget this vaccine is being promoted by our schools, Department of Education, the Health Service Executive Ireland (HSE) and WHO so one would think it must be good for all our children. Surely these reputable organizations wouldn’t take any chances with the lives and health of our next generation. I was satisfied I had done my research and taken all necessary precautions.

On the day of Laura’s first vaccination and indeed the following two injections, I was called to the school as Laura was feeling weak. This was to be expected as Laura was always squeamish about needles. In fact I had to do a lot of talking with her about the necessity of this vaccination to convince her to go through with having ‘a needle’. On the day there was also a lot of scare mongering amongst the students so I probably took it for granted that this had raised their anxieties and caused several of the girls to feel weak and unwell.

The vaccinating nurse told me to take her home, let her rest and she would be fine.

In the months that followed, Laura started phoning from school complaining of feeling unwell, faint and dizzy. We thought she was starting to experience menstrual problems for the first time although her periods were well established and not problematic before. The family doctor prescribed medication.

Laura was becoming tired all the time, her short term memory and concentration were deteriorating. She also started to experience food intolerances for the first time, in particular, yeast, gluten and dairy. Laura suffered visual disturbances and noise sensitivity. Burning muscles and joint pain were her constant companion. She was unable to continue with sports.

Before all this happened Laura played basketball for Drogheda Ladies and the school team. She loved to Kayak at the weekends and during school holidays, Laura was super-fit, active and happy. All extra-curricular and social activity had by now become impossible for her.

Even friends stopped calling as she didn’t have the strength to go out with them. Slowly life as Laura knew it was changing.

To put things in perspective, my mother in her 80’s was going out to day-care and Laura was lying in bed or on the couch. In fact on many an occasion we had to use my mother’s wheelchair for Laura when she hadn’t the energy to walk. It was plain for anyone to see something was very seriously wrong.

We started to visit our GP more and more although whilst growing up Laura only visited our doctor on a few occasions. No one seemed to have any idea what was going on, tests and more tests, nearly every box ticked on the blood forms. Every kind of sample you could imagine was requested, yet none of the results showed up anything. They all came back clear, indicating Laura was in good health.

Therefore no help, advice, medications or supplements were recommended. On every occasion we returned home deflated and our hopes dashed again and again.

I could no longer sleep at night with stress and worry. Instead, I found myself up in the middle of the night logging on to google looking for answers. Night after night I lay in bed racking my brains trying to figure out what happened. When exactly had things all started to go wrong and why?

Then in early 2012 for some reason the HPV vaccine came back to my mind. Could it possibly be the cause of all Laura’s health problems, the vaccine that I was so reassured about? Laura had been an exceptionally healthy child before this. And maybe I was very foolish to dismiss her weakness after the injections. I thought things were now fitting into place, the timing of her Gardasil vaccinations and the onset of symptoms etc.

As soon as I brought my suspicions to our family doctor he wrote a letter referring us to a consultant paediatrician, who after 5 minutes of interview dismissed my fears about the HPV vaccine and reassured me yet again that this was a very safe vaccine, he diagnosed ME/CFS and told Laura she would be better in 6 months.

Thank God we thought, light at the end of the tunnel and wonderful news – it’s not long term vaccine damage.

Laura just about managed to sit her junior certificate exams a month after this diagnosis with special provisions made for her by the department of education. Her results were very good under the circumstances but definitely did not reflect the top honours student she always was.

Six months started to roll on to 12 months and Laura was definitely not getting any better. In fact, by September 2013 she was no longer able to attend school, only now and again for a half day or a couple of classes at a time.

Weeks at a time went by with Laura lying in her bed, exhausted, but unable to get any kind of rejuvenating sleep, racked with pain and barely able to communicate. The weeks became months, we saw less of her around the house as she was spending most of her days in her bed. At her lowest point I found her younger brother Conor spoon feeding her as she didn’t have the strength or energy to feed herself. She moved into a spare bed in his room as she was lonely and afraid in her room on her own.

Meanwhile I kept researching ME/CFS trying different supplements etc. to try to help her, not all of her symptoms fit under the ME/CFS heading. That HPV vaccination came back to my mind again and again as being the cause of all her problems.

One night I typed in ‘HPV vaccination injury’ – ‘injury’ being the all-important word. This search lead me to hundreds of articles and sites on serious adverse reactions and long term side effects caused by HPV vaccination and in particular Gardasil, the very one Laura was injected with.

There it was right in front of me on my screen, thousands of girls like my Laura with similar symptoms, some worse and some who had actually died. I can barely read any more of these stories as I find them so painful. I’ve cried more than I thought ever possible. My God, the immeasurable guilt I feel every day for signing that consent form.

It’s now four years since Laura received her Gardasil vaccination. Through educating ourselves with useful information posted by other vaccine injured girls and their families, Laura is making improvements.

She follows a very strict diet, is trying to detox her system of heavy metals found in this vaccine. She gets acupuncture and vitamin B12 when she feels these will benefit her. She also found very high doses of top quality Omega 3 EPA to be very helpful.

Laura says, every year she feels sick to her stomach when she hears the first years being called to the hall for their HPV injections. Who could blame her? If she does recover from this and please God she will, Gardasil has taken away years of her life and experiences that can never be replaced.

There’s also the added worry of her fertility. Many of the other girls have experienced ovarian failure as young as 16.

As for Laura’s future, it is still unclear. She has made some improvement and is into the final 18 months in secondary school but still missing an awful lot of classes and even several days at a time. Every week she prioritises what classes she needs to attend and when she can fit in rest periods. She has her sights set high in terms of college points.

At this stage she herself feels she may have to defer for a few years. This is yet another blow but Laura rarely complains, just tries to stay realistic and upbeat…. I’m her mother and I’m no fool. I know there are times when it’s all a front because she doesn’t want to see me upset.

If we have learned anything positive from this horrendous life altering experience, it is that there are some very good people out there eager to help who have taken a genuine interest in Laura’s plight. But unfortunately no one seems to have the cure.

Please God by sharing our experiences we can all help one another.

Read this article in French here.

Karen and Laura, what strong woman you are and great examples to many others. I am sorry you have faced such a distressing and life-altering situation. Your strength and integrity shows through. No doubt, others will read your story and will be spared from a like trial. It is very kind for you to share such personal details.

I feel inspired and so will others to face life’s challenges head- on, and through working together we can minimize the hard effects. I know that as you place your burdens on the Lord, he will lighten the load and guide you on paths that you probably don’t even know exist.

I am grateful you are in touch with the team at SaneVax. They have huge hearts and have worked tirelessly to assist others in like situations. I also have a Featured Doctors section in my menu that has doctors who are familiar with vaccine damages and how to heal.

God bless and please enjoy the musical art below. Your friend, jen

Article in it’s entirety, is compliments of www.sanevax.org

Judges demand answers after children die in controversial cancer vaccine trial in India#cdcwhistleblower#HearThisWell#Vaccines

January 21, 2015January 21, 2015 jlvranes Leave a comment

There have been over 37,000. adverse events and 214 deaths from the Gardasil/Cervarix vaccines with no evidence of any benefit from the vaccine. These figures are off of the November 2014 VAERS report and estimated to be only 1-10% of actual cases.

By GETHIN CHAMBERLAIN IN INDORE, INDIA,

Tribal girls were given shots of cervical cancer vaccines during trial
Children given Merck’s Gardasil and Cervarix vaccines
Petitioners also asked judges to investigate trials of new drug Gardasil 9
Drug has allegedly caused side-effects in children as young as nine
Investigation claims children were used as unwitting human guinea pigs
Supreme Court has given the government one month to provide answers

Judges in India’s Supreme Court have demanded answers after children died during a controversial cervical cancer vaccine trial.

Young tribal girls received shots of pharmaceutical company Merck’s Gardasil vaccine and Cervarix, manufactured by GlaxoSmithKline.

The vaccines are given to girls as young as nine in many countries – including the UK and the US – to protect against the human papilloma virus, one of the major causes of cervical cancer.

But the Indian court yesterday heard a challenge by campaigners who claim the study – funded by the Bill & Melinda Gates Foundation – failed to obtain the informed consent of the children or their parents.

They say that a ‘study’ carried out for the foundation by a US organisation was in fact an illegal drugs trial.

Continue to the Article Here

http://www.dailymail.co.uk/

My daughter’s life altering changes after Gardasil#cdcwhistleblower#Family#iBelieve

January 14, 2015January 13, 2015 jlvranes Leave a comment

By Shanna DeJaynes, Okay Oklahoma

My daughter lives a Gardasil nightmare. Our family has suffered along with her for almost three years. I refuse to be silent any longer. I share my daughter’s story as a warning to others – Gardasil is not safe for everyone – please, don’t make the same mistake we did.

At 13 years old my daughter, Breanna DeJaynes, was involved in volleyball, basketball and cheerleading at school. She was very outgoing and not shy to make new friends at all. She was a good student, hardly ever missed school and got good grades. She was on the honor roll for several years in a row. Breanna was very active both in and out of school. I could hardly keep her inside; when she wasn’t out practicing or in the classroom, she was with her friends. In short, Breanna was a healthy, happy, all-American girl before Gardasil.

She received her first HPV vaccine injection in April of 2011. Within a couple of days she started having some mild symptoms like dizziness, headaches, cramps in both her legs and arms, passing out, getting over heated easily and complaining that the arm she had the injection in was achy at times.

Every time something happened we would take her to the doctor. If it happened at school they would call 911 and have EMS come and rush her to the hospital (it was school policy to call 911 whenever something happened at a school-sponsored event).

We were always told she was just overdoing it with her sports, she had just hyperventilated, or that she had stood up too fast, or she had taken too hot a bath or shower, got overheated, wasn’t drinking enough water, was dehydrated and so on. We were told everything under the sun. The possibility that her new symptoms could be related to the HPV vaccine never crossed my mind at the time.

As the weeks passed her symptoms continued to get worse. She received her second Gardasil injection in June or July of 2011 and things got worse than before. Her headaches got so severe she couldn’t even stand to be in light, it would make her nauseous. The headaches were always in the same spot on her head in the frontal lobe. Her leg and arm cramps got worse, passing out continued, then she started having seizures both with and without memory loss, at times forgetting her friends, family and so on.

She suddenly couldn’t handle being in large crowds, it would make her so nervous she would start to cry hysterically and hide behind whoever or whatever she could. When she had a seizure it wiped her out to the point where she couldn’t walk or even talk sometimes due to being so confused and disoriented, not knowing where she was most of the time.

She could no longer concentrate at school due to the extreme headaches and body aches, feeling sick, or focus on school work. When she had a severe seizure she couldn’t remember what she had learned the week before, sometimes even the day before. Breanna would get exhausted very easily, be confused, and have involuntary tremors, muscles spasms and so much more. The list of symptoms goes on and on.

In early October 2012, she had over 15 seizures in one day so I was called home from work. I decided I was fed up with taking her to our local hospitals and getting nowhere. I took her to the Children’s Hospital in Tulsa.

She was admitted and put on an EEG monitor for several days. As they were doing the intake paperwork for her to be admitted they had asked all the common questions, for example: ‘Had there been any changes in her routine? Had we had an accident of any kind? Had I recently changed anything at home? Did I think that she was doing too much activity wise?’

The answers to all of the questions was of course ‘no’. Nothing had changed EXCEPT for the fact she had been given the first and second doses of the HPV vaccine, Gardasil.

After the doctor left the room, a nurse asked if I had researched information about Gardasil and I told her no, I had not because I was told that it was “perfectly safe.”

With the high risk of cancer in our family I thought “Why wouldn’t I want to try and prevent her from getting cancer in the future if that was something that I could do? It could possibly save her life,” or so I thought!

The nurse continued to talk to me about the vaccine and told me to go home and do some research on the Gardasil vaccine.

As Breanna sat in the hospital for the next several days, she only had one seizure. It happened before they got her hooked up to all the monitors because of course it took them forever to get us up to a room and get things going for the monitor. But after she had the one on the hospital floor she was assigned to, every nurse and doctor on duty on that floor was there in a heartbeat. And THEN they put in a rush order to get her hooked up to the monitors as soon as possible.

One morning the doctor asked if it was ok to speak to Breanna alone. I said yes. I was sure that it would be fine. I had no idea what was going to take place.

As he talked with her, he started accusing her of making all this up, that it was all to get attention, it was all in her head and she needed to grow up and stop playing games.

After he finished talking to her I went back into the room. I found her in tears, shaking and trying to pull all the wires off. She cried, “Please take me home – I don’t want to be here anymore.”

It took me a while to calm her down, but I finally got her to tell me what the doctor had said to her.

At this point I was ready to have him called back into the room so that I could give him a piece of my mind AND my fist. My blood was boiling by this point. How dare they treat my daughter this way!

I called the nurse in and asked to speak with a supervisor. They came in a short time later and were extremely apologetic.

I told them I did NOT want that physician to come back into her room under any circumstances or there was going to be a serious problem. I also demanded a different physician for her.

A new doctor came and said there was no activity that had showed up on the EEG testing while she was hooked up to the monitors and sent us home.

We were referred to a neurologist and many other kinds of specialist during this time. After being released from the hospital her symptoms continued to get worse. She was prescribed one seizure medication after another with no relief for over a year and a half. At that time the neurology visits literally consisted of us just walking into the room, her asking how my daughter had been and saying there would be a different medication waiting for her at our pharmacy. It literally took us longer to find a parking place than the time we were in the room with the doctor.

I finally got to the point where I understood we were getting no help. I took Breanna back to her pediatrician and demanded that he send her to another neurologist. I began to ask questions about whether her new symptoms could possibly be related to the HPV vaccine injections she had.

I was always reassured there was no way her current condition was associated with the HPV vaccine no matter what I told them. It did not seem to matter that she had none of these symptoms before she received Gardasil. It did not seem to matter that Gardasil had been the only new thing in her life when this nightmare began.

We started to see the new doctor and of course he ordered all the same tests which had already been done, office and in-home EEG’s, EKG’s, blood work, urine tests etc. He got the same results – everything was negative.

Breanna started to suffer in school due to the memory loss with the seizures, cramping tremors, extreme headaches etc. to the extent that it was causing her grades to go down. She couldn’t remember her school assignments. She had to quit all sports because she was just too weak to do any of that anymore.

Not understanding what was going on with her, most of her friends started to abandon her and not have anything to do with her any more. This caused her to go into a deep depressive state where she wouldn’t leave the house for months. She was too embarrassed about what people would say and worried that she was getting made fun of. That was very hard for her to deal with.

She has continued to miss school and not be able to complete a lot of her work due to her seizures and memory problems. We are now in the process of trying to get her in an online school so she can work at her own pace when she feels well enough to be able to do it. This way she can work at any time of the day so hopefully she will be able to graduate on time. One thing we are thankful for is that we have a good school. They have been very supportive of what is going on with her because they realize it is a medical issue. But when she has any kind of episodes at school I have to go and pick her up right away because of the potential liability for the school if she were to get injured at school.

The doctors have recently taken her off seizure meds but that simply made her seizures worse.

I lost my job of over 7 years because I have to be available to get her from school at a moment’s notice, be here to care for her and watch over her 24 hours a day. Right now, she has seizures 4 or more times a week, sometimes having more than one a day. She isn’t allowed to take a shower or bath without someone there with her. As a 16 year old teenager that is particularly difficult because she can’t have her privacy. As a mother I need and want to be there especially when she has a seizure and is in a state of confusion, when she has them so bad that she loses her ability to remember anyone or anything. We never know when the seizures will come or how long her memory loss will last so I have to be here at all times. Until this nightmare is over, it is impossible for me to hold down a job.

We continue to struggle with her every day to deal with whatever her issues may be that particular day. Breanna has accepted the fact that this is something she has to learn to cope with until we find someone who can help her. We struggle to help her make it through every single day. It is not easy, but we get through it as a family.

It breaks my heart to know my daughter had none of these medical issues until after she received those two shots of Gardasil. As a mother, I struggle daily with regret. I allowed my daughter to get this vaccine thinking I was doing the right thing. As it turned out, nothing was further from the truth.

Seeing your child suffer on a daily basis without the ability to do anything to help them is something no parent should ever have to deal with after a routine vaccine. I only wish I could turn back time so she could have the life she had before being injected with Gardasil.

Now that I have been able to share Breanna’s story I have discovered she isn’t the only young lady, or young boy, that has suffered with issues from this vaccine. It just breaks my heart to know there are so many girls who have very similar or even worse symptoms than those Breanna struggles with.

I am just thankful I did some research before I took her to get the last shot of Gardasil.

Thank you SaneVax for letting me share Breanna’s story. It has been a long road and will continue to be until she gets proper care and this poison out of her body.

Since first coming out with Breanna’s story I have been in contact with many other families who are going through the same kinds of issues or worse. It’s overwhelming, but comforting at the same time. We know we are not alone. Getting to speak with other moms who have been where we are is nice.

There are people that just don’t understand what Breanna’s issues are. I just pray for those people and hope that they never have to deal with what we deal with every day of our lives. I pray parents research all aspects of HPV vaccines before exercising their right to informed consent.

I pray no other parent makes the same mistake I did – allowing my daughter get the HPV vaccine before doing MY homework!

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

Shanna, my heart just aches as I read what Breanna and your family has suffered through these past few years. I am so sorry that you had a physician demean and verbally attack your daughter. It is hard to believe that there are some who choose an industry that is based on caring for others that lash out to the most vulnerable. Just unthinkable, though it goes on all too frequently.

I am so glad that Breanna has a mother like you. I think this is one of the most difficult trials, for teens and their families right now, worldwide. Thanks to people like you, the word is getting out and many will avoid this trial or stop and limit the number of shots and negative outcomes.

Breanna you are such a bright light and I hope you hang onto the hope of something better. Keep the Lord by your side and the best possible outcomes will show forth.

As you know, many in the healthcare industry are unaware of the symptoms and care following a Gardasil shot. I have a menu option on my blog with Featured Doctors that have experience with treating vaccine injuries and overall strengthening of the immune system. SaneVax.org also has wonderful connections with doctors that have proven records of treating vaccine injuries with success. The team at SaneVax is great to work with and you are in good hands with them.

I would like to share an artistic gift with you. I hope this takes your mind away from your cares and brings you some light and joy into your life right now, and Breanna I hope you just let any hurtful words just wash away. Always remember the bright, beautiful and strong girl you are. You are amazing!! You will be able to rise above this time in your life. Just Believe. Your friend, jen.

Gardasil: I should have researched first#HPV#Family#retweet

December 19, 2014December 19, 2014 jlvranes Leave a comment

By Paula from Alzey, Germany

When I received my first Gardasil-Vaccination/Immunization at the beginning of the Easter holidays in 2014, I felt very uncomfortable. It felt as if I had been injected with something viscous, like dough or batter.

The spot in which the needle was pricked, was very thick and hard. Furthermore, it hurt and I directly fainted at the ambulance. I was put on a lounger and after a short while I was able to stand up again. We didn`t do anything to combat the pain because I thought it`s something like a bruise.

One day later: I stood up like always, but I had a strong giddiness and felt as if I had a glass dome above my head. Three days later I was experiencing palpitations during the evenings for around one week. Also I often had chills and would shiver a lot. Afterwards I sweated and my right leg and right arm were vibrating (nervous twitching).

In school I was distracted and couldn`t concentrate. This lasted for a few weeks. For eight weeks I ran a fever every day. The doctor called it sub-febrile temperature. The whole thing was so bad that I could not sleep, stand up or eat anything. The vaccinating house doctor told me that my discomfort had nothing to do with the vaccination.

I had to give up my favorite sport because I was not able to take part in training anymore. Since I missed a lot of school lessons (classes), I have to catch up a lot. This is very exhausting so my family and I decided to cancel my sport school membership to fully concentrate on my academic studies at school. Even though I felt well again it would be too much at the moment.

But back to my bad time after the vaccination!

My blood was tested two times and my Immunoglobulin M was much too high. The doctor prescribed some antibiotics because she had no other solution. She didn´t want me to get a bacterial infection in addition to the virus infection.

It had been found out that the Gardasil-Vaccination triggered Gluten and Histamine hyper-sensitivity. Whenever I eat normal bread I get a bad stomach which will last until the next day.

In May I went for the first time to the osteopathic practice of Chr. Plothe. There, my problems were taken seriously for the first time. Everything was explained to me in detail and they carried out a lot of tests (blood, etc.). I was given the services of a dietitian and my therapy was discussed. I also had to take some dietary supplements, was detoxified, got infusions and was treated by an osteopath. Step by step I felt better.

In general, I missed school for forty days. Often, my mother brought me to class for only two lessons, because I was not able to handle more. Simply the bus drive to school was impossible for me.

It was remarkable that my palpitations (which I had only for one week in the beginning), the shivering and the twitching of my leg and my arm strongly reoccurred shortly after the first Glutathione infusion. It felt as if my body worked very hard. The high doses of Vitamin C infusions which I was given in the clinic helped me a lot. Moreover I felt much better after the osteopathic treatment.

Since the first week of summer vacation I feel very well again. The glass dome above my head disappeared. I have new energy and I am able to stand up in the morning.

After the holidays I was in school for one complete week. I am able to keep attending class and to do my homework afterwards. Two months ago I thought that I would never get healthy again.

I am so thankful to have been able to go to this clinic and receive this treatment and I would highly recommend it. It saved me from having long-term health issues.

How I wish we had looked into the side effects which can occur with the Gardasil vaccine before agreeing to being inoculated.

I strongly recommend that every family does a thorough investigation before deciding to use Gardasil. Check the internet. You will find many thousands of young people with serious health issues after being vaccinated with Gardasil.

I am one of the lucky ones who was given a treatment that helped me recover. Many others have not been so lucky.

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

Paula, I am so glad you found Chr. Pothe’s Osteopathic office. They sound like they must have been a godsend, when you needed them most. Thank you for taking the time to help others avoid a brutal situation, and help direct those, in need of care.

You are a very determined individual, and I hope that your future opens up to beautiful opportunities for you. Below is a little artistic gift that I hope you enjoy.

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

December 11, 2014December 10, 2014 jlvranes Leave a comment

By Annette, Melbourne, Australia

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.