Category: HPV vaccine injury

My Children are Vaccine-Damaged; are Yours?#android#iPad#retweet

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by Michelle Goldstein

I was raised like most Americans. Doctors were highly respected in my parents’ home and their authority on health matters was not questioned. My parents followed their physicians’ advice on healthcare and I was no different when raising my own children.

I was careful to follow the health and dietary recommendations when my children were young and I believed that vaccines would keep my children safe from disease.  In fact, I believed wholeheartedly that the more vaccines we had, the better protected my family would be. Out of love, I gave myself and my children every new vaccine available. I consulted with our physicians and with full trust followed their advice.

The Vaccine That Woke Me Up To Vaccine Dangers

After consulting with my trusted obstetrician, who had delivered all three of my children, along with my pediatrician, I made the fateful decision to vaccinate my two daughters with the HPV vaccination series.  Several months later, one child developed a serious case of the debilitating autoimmune disorder, Crohn’s disease, which robbed her of several years of her childhood. We continue to battle this ravaging disease.

It took many years and countless consultations with integrative, holistic physicians before I recognized the link between the HPV vaccination and my daughter’s illness. To be honest, there was only one holistic physician, who specialized in autism, who helped us make this connection. The many others, including a certified functional medicine doctor, failed to connect these two events.

I now believe wholeheartedly that the HPV vaccine and my daughter’s development of a life-threatening autoimmune disorder was no coincidence…

Norway: Force-vaccinated with Gardasil#android#iPad#retweet

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By mother Stine-Marie Buer Hasvold. Skien Norway

I didn't consent to Gardasil

I didn’t consent to Gardasil

Caroline was born in 2000 and is now 15 years old. My daughter was very sociable, full of energy and always together with her many friends – running, cycling and playing football. She always had a good appetite.

The only information we were given when the Gardasil vaccine was offered was that it may cause influenza like symptoms which were temporary, just like other vaccines for children.

Even though I had written in the notice book and given information that if she did not want the vaccine, then she MUST NOT be given it – Caroline was held by one nurse whilst another nurse administered the vaccine!

A few days later, half of Caroline’s face became paralyzed. She was admitted to the local hospital where tests were done but they found NOTHING wrong.  I told them I was sure Gardasil was the cause, but they did not listen.

This was the only examination Caroline has had since Gardasil administration. We have not had any follow up because the hospital and doctor say that the problems are mentally caused. They maintain that the symptoms occurred six months after Caroline’s grandmother died; therefore, the sorrow of her death triggered it all!

Needless to say, Caroline only had the first injection of the three that are recommended.

No doctor will listen. They say that Caroline needs mental therapy for her sorrow after my mother’s death. She has had no more tests or treatment because no one believes us. Now she feels pain in her whole body and just wants to sleep. She feels ill all the time. She hardly manages to do anything, has poor memory, heart palpitations, stabbing pain in her chest, and sometimes has breathing difficulties. She often has headaches and now has a poor appetite. She gets tired just by going to the toilet. She can’t walk or cycle any particular distance – her legs go weak and lose feeling. She is bedridden most of the
time.

There has not been any medical help and no support or understanding from Caroline’s new school.
She now goes to school as long as she can but on the days when her legs are too weak I drive her there. She has had eight days and 24 hours absence this spring. She has only attained 2 as her final grade. She was absent from school 15 days in the autumn. Her school work takes a long time, she finds
it difficult to concentrate because of pain and she feels very tired both mentally and physically. Her sight in one eye has become weaker.

Hanging onto hope!

Hanging onto hope!

Caroline has been told by her teachers that she is lazy, which adds to her suffering and is heartbreaking for us as we know how much pain she has and how hard she is struggling. If only the teachers would believe that Caroline is ill and would try to understand.

Some parents say that we should not tell others about the risks from Gardasil because they believe that the vaccine prevents cervical cancer, but we have heard that  proof that the vaccine prevents cervical cancer will not be available for many years.

The nurse who administered Gardasil against my daughter’s will came to our home and contacted us several times. She told us they were extremely afraid that we could scare other children about taking the vaccine and that we MUST NOT mention the vaccine in connection with our daughter being ill.

We hardly hear about other girls in Norway who are suffering after Gardasil, but there are reports of thousands in other countries across the world and many of them are ill with the same symptoms as Caroline.

We are very grateful that Caroline’s story is being published so that it will reach out to many others to warn about the possible dangers of the vaccine.

I am beginning to lose hope for Caroline’s future as she is gradually becoming more and more ill. Maybe HPV infections do take some people’s lives; maybe they don’t. All I know is I would rather have watched my daughter enjoy her teenage years instead of spending those years worrying about her future.

Please DON’T let your children be test subjects for a vaccine which has ruined the lives of so many.

Read this article in French here.

This article in it’s entirety, is compliments of Sane Vax

Stine-Marie, thank you for sharing Caroline’s story with us.

We are amazed with your fortitude and strength.  Thank you for also letting others know of the risks with the HPV vaccines.

I hope you have a health practitioner that is actually helping Caroline at this point.  If not, here is a link to some of my Featured Doctors with experience in this area.  

Sane Vax also has reputable, experienced health practitioners that they can refer.  A lot can be done, even from a distance.

Medical Professional Listing

Please hold strong.  Let the Lord take your hand.  He loves you, knows your pain, and will guide you.

Your friend, jen

Here is a little musical gift that I hope eases your stress and lifts your hearts at this time.

 

Is HPV Vaccine Safety an Illusion Maintained by Suppression of Science?#android#iPad#retweet

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By Norma Erickson

Breaking News: On January 14, 2016, Dr. Sin Hang Lee sent an open letter of complaint to the Director General of the World Health Organization, Dr. Margaret Chan, charging members of GACVS, the CDC, the Japanese Ministry of Health, Labor and Welfare, and others with manipulation of data and suppression of science in order to maintain the illusion of HPV vaccine safety in the face of valid contradictory evidence.

According to Dr. Lee’s letter, a series of emails recently uncovered via a Freedom of Information request submitted in New Zealand revealed evidence that Dr. Robert Pless, chairperson of the Global Advisory Committee on Vaccine Safety (GACVS), Dr. Nabae Koji of the Ministry of Health of Japan, Dr. Melinda Wharton of the CDC, Dr. Helen Petousis-Harris of Auckland University, New Zealand, and others (including WHO officials) may have been actively involved in a scheme to deliberately mislead the Japanese Expert Inquiry on human papillomavirus (HPV) vaccine safety before, during and after the February 26, 2014 public hearing in Tokyo.

The complaint letter states that the emails provided clearly demonstrate this group of WHO officials and government employees charged with the responsibility of advising the expert committee from the Japanese government on HPV vaccination safety knew before the February 26, 2014 Tokyo public hearing that one of their own experts showed scientific evidence that HPV vaccination does increase cytokines, including tumor necrosis factor (TNF), particularly at the injection site compared to other vaccines. Yet, they chose to suppress this information at the public hearing.

Of course, this piece of scientific data which was known to all members of the group is also missing from the GACVS Statement on the safety of HPV vaccination issued on March 12, 2014.  Unfortunately for medical consumers, this is the same GACVS statement currently being used to assure health officials, political decision makers and medical professionals around the world there is nothing to worry about when it comes to the safety of HPV vaccines.

  • Dr. Lee concluded his letter of complaint by clearly stating that there is at least one known mechanism of action explaining why serious adverse reactions occur more often in people injected with HPV vaccines than other vaccines, and why certain predisposed individuals may suffer a sudden unexplained death as a result. It appears this is part of the information the ‘experts’ deemed necessary to suppress.

Dr. Lee states:

Those whose names appear in my complaint and any who blindly dismiss valid safety concerns in order to continue promoting HPV vaccinations should be held accountable for their actions. There is no excuse for intentionally ignoring scientific evidence. There is no excuse for misleading global vaccination policy makers at the expense of public health interests. There is no excuse for such a blatant violation of the public trust.

Read Dr. Lee’s letter of complaint here.

Attachments to letter:

Translations:

This article in it’s entirety, is compliments of Sane Vax

Vaccinating Without Parental Knowledge Soon To Become The Norm Across The World#android#iPad#retweet

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Health officials in the U.S, U.K, Canada, Australia and around the world are officially crossing into dangerous territory with parents when it comes to vaccinations. Not only are public health entities habitually and deliberately failing to inform the public of their right to refuse vaccines in both school and work settings, but they are working towards mandatory vaccination protocols which will allow officials to conduct childhood vaccinations without any parental consent at all.

It was just a little over one year ago when the pharmaceutical industry, the Department of Health and Human Services, and Centers for Disease Control allocated millions of dollars in funding to establish vaccine clinics in public schools, causing a huge uproar from concerned parents.

The RAND Corporation, paid by Sanofi Pasteur, outlined how to turn schools into vaccine clinics, which critics claimed will inevitably poison children with multi-dose vaccines.

These school based health centers (SBHCs) are located in school…

Continue to the Article Here

http://preventdisease.com/

Recovering from my Gardasil Nightmare#android#iPad#retweet

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By Lisa Pipella, from Spokane WA

My Gardasil Nightmare is Nearly Over

When I originally wrote my Gardasil story as a cautionary tale for others, I thought the worst was over. I had battled for almost six years and was left with only periodic numbness/tingling in my hands to deal with at that point. I believed the worst was over and I could begin to get on with my life. That was in October of 2013.

In 2014, the roller coaster ride began again. My hands became worse; the tingling and numbness traveled to my legs. I would have moments of paralysis forcing me to rely on crutches to get around for a few days each month. My sleep patterns became irregular. I would stay awake for 4 days straight before collapsing from sheer exhaustion and physical weakness. The numbness and tingling I previously had in my hands progressed to tremors that never stopped, even when I was sleeping. Tremors so bad they stopped me from successful photography, hindering my ability to complete my home-based projects or even use everyday tools.

So, I began a new journey visiting more doctors, doing more tests. After some careful observation, we were able to pinpoint the exact time frame during which my symptoms got worse and I would lose normal function of my hands and feet along with the annoying hot pins and needles feelings. It was around the time of my menstrual cycle.

After determining this, I went to see a chiropracter for the first time where I was given some good lifestyle advice. I started on some new detox programs and parasite cleanses in hopes of seeing some improvement. I had been eating clean organic foods but my blood sugar would still peak and dip causing moments of confusion, mood swings, the shakes and weakness. I was able to correct these problems through a new diet that cut out all sugars. It was a great feeling to eliminate those symptoms once my blood sugar was corrected.

Shortly after, I was able to meet with a new doctor about my symptoms to try and gain a different perspective. She gave me a clinical diagnosis of Guillain-Barre Syndrome. Believe it or not, it was somewhat of a relief to have a diagnosis that would explain the majority of my limb symptoms including why my hands were stuck in a claw position.

Next, I went to get a full blood panel to see what that would tell me. Almost everything came back normal. This was my 3rd blood panel in the years since my Gardasil injections. It only revealed that I was low in B6 and D3. So, for the first time in my life, I started taking supplements. They did nothing for me and none of us could figure out why.

I bought several books and spoke to several amazing Gardasil-injured girls  who found healing using different methods. But, none of the methods would work for me. I was growing tired of visiting so many doctors and having to explain everything over and over again. But, I was not going to give up.

I spent all of 2014 seeking answers only to end up having a major life-threatening stroke in January of 2015. I was sitting on the couch and felt a really bad throbbing ache behind my left eye. Then, all of a sudden, I had a ”bursting” sensation. I screamed for my husband and he sat with me. I was unable to speak or even understand where I was at. I was screaming in pain as I felt a traveling sensation go up and over my left ear, resting at the base of my skull. I ended up going to bed because the pain exhausted my entire body.

I woke up in the middle of the night from the lingering pain and experienced a stroke. My left eye was fully dilated and everything was confusing. I immediately went and got an MRI. It came back ”unremarkable.”

Then, I got my eyes checked to see if anything was wrong. Those tests also came back normal.

I felt like I had come to another dead end. What if I did not survive my next stroke? My children would be motherless.

So, I set out on another research adventure and put the doctors aside. They were not finding anything and I was not healing.

Is the answer in your Methylation Cycle?

I work with many parents in the autism community and entered into a conversation with some of them about genetics and genetic mutations. I was absolutely fascinated.

They were talking about MTHFR genetic mutations which were identified by the Human Genome Project in 2003. MTHFR stands for methylenetetrahydrofolate reductase. This mutation is thought to be a key to all disease, autoimmune disease, and neurological issues in addition to making people more susceptible to adverse reactions to vaccines, medications and supplements.

If we look at immunogenetics and adversomics we can begin to understand why certain people have adverse reactions to vaccines. Vaccines are causing genetic expression. The methylation cycle is very important in the human body. It also dictates how the immune system functions.

After a few months researching, I ended up ordering a test from 23andme.com. I sent my spit test in and the results came back. Guess what? I have the MTHFR C667T mutation along with other mutations that contribute to stroke (Val12Met) and cancer (BRCA). I also have the ’Fragile X’ gene (FMR1). The results were overwhelming.

I immediately sought out additional information on this and joined a MTHFR group. I started out by trying a B12 supplement tailored to my genetic mutation(s). It was called Methylcobalamin. The first time I took it, it knocked me out flat. I was wiped out for several days – almost as if I was in an alcoholic stupor. The fatigue was terrible. I felt betrayed.

But then I switched to taking it before bed, and what do you know, I slept the entire night! So I was taking this every night because research says you must be on it regularly to keep in in your system. Every day was a new milestone for me. My hands unclenched from their claw positions. My legs stopped tingling. I could feel my feet for the first time in a long time. My hands were able to feel again. My tremors, paralysis, burning, tingling, pins and needles sensations dissipated a little each night until they were no more. It was almost unbelievable. I cried tears of joy!

After regulating my methylation cycle with the B12, I decided to try the supplements again. I started taking chlorella, selenium, vitamin D3, Lithium Orotate and probiotics. It was as if every single supplement kicked in all at once.

I was happy again. I could keep up with my children. I finally have my life back!

My Gardasil injections were in 2007. This is the first time in 8 years I can finally say I feel ”normal” again. So far, it has been three entire months of being healed. I believe my Gardasil Nightmare is finally over.

I would like to take a moment to thank the autism community and particularly The Thinking Mom’s Revolution. Without them I would have never known the importance of the methylation cycle, MTHFR, and glutathione.

Please understand that what works for one Gardasil-injured girl may not work for another. Sometimes you have to take very slow steps when introducing new healing methods in order to avoid further injury. It was a very long and slow, trial and error process discovering which methods would work for me. The amount of detoxing I did through the past year set the stage for further healing.

I highly recommend genetic testing as a good place to start. It gave me a blueprint to go by; maybe it will do the same for you!

This article in it’s entirety, is compliments of Sane Vax

UK AHVID responds to EMA conclusion that HPV vaccines do not cause POTS or CRPS#android#iPad#retweet

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BY

AHVID loco

By Steve Hinks email steve@hinksfamily.co.uk)

The European Medicines Agency has today released the Pharmacovigilance Risk Assessment Committee’s conclusion of their review of HPV vaccines in relation to two serious neurological conditions, Postural Orthostatic Tachycardia Syndrome (POTS) and Complex Region Pain Syndrome (CRPS).  The PRAC assessment concluded that the available evidence does not support that CRPS and POTS are caused by HPV vaccines.

The UK Association of HPV Vaccine Injured Daughters (AHVID) is extremely disappointed by the committee’s findings and concerned by the lack of transparency and opportunity to scrutinize the evidence considered by the PRAC before the Committee for Medicinal Products for Human Use (CHMP) adopts the committee’s findings.

Freda Birrell, Chair of AHVID said:

“Groups across Europe representing families of girls suffering new health conditions following HPV vaccination will naturally be very disappointed with this investigation and we are particularly concerned that the evidence considered by the PRAC will not be made available for scrutiny until after CHMP has reviewed the PRAC Assessment and adopted the decision. We have even been denied a request to know which experts submitted evidence. This shroud of secrecy is very concerning – something is leaving these girls seriously ill! We are however, very encouraged by the recent award of research funding from the Danish health authorities to a Danish team of doctors, to research adverse reactions to the HPV vaccination, and we await the results of that research with anticipation, particularly in light of recent reports from Denmark estimating 1 in 400 girls are suffering serious adverse reactions to the HPV vaccination.”

AHVID recently conducted a survey of members for information to submit to the EMA review.  The findings from nearly 100 members highlighted massive under-reporting of adverse reactions by health professionals, a failure of health professionals to recognize and acknowledge adverse reactions and the difficulties experienced getting a POTS diagnosis, with most girls waiting for more than two years.  Shockingly, the survey also found over 90% of respondents were initially told by their doctors that their symptoms were psychological.

The PRAC appear to have based their decision on their statement that the available estimates suggest natural rates of both POTS and CRPS to be around 150 girls per million in the age range of 10 to 19.  AHVID are unable to comment on this statement because the request for copies of evidence and reports considered by the Committee have been refused until the Review is finalized, but the group remain convinced the HPV vaccination is resulting in girls developing serious autoimmune and neurological conditions, including POTS and CRPS.

The PRAC makes reference to an overlap of CRPS and POTS symptoms with Chronic Fatigue Syndrome/Myalgic Encephalomyelitis and the ‘large published study that showed no link between HPV vaccine and CFS’, which the Committee considered particularly relevant. The study ‘Bivalent HPV vaccine and the risk of fatigue syndromes in girls in the UK’ was undertaken and authored by MHRA scientists, it was looking only at the Cervarix vaccine, used data from the CRPD database which is collected for clinical management, not research, was open to confounding and selection bias and was at the mercy of the accuracy of GPs inputting accurate diagnostic codes. The study would also have been unlikely to have picked out cases of POTS or CRPS and would certainly have missed the many girls with POTS who were initially misdiagnosed with anxiety or psychological conditions.

AHVID will continue to support families with girls suffering new health conditions following HPV vaccination and will continue to fight for better treatment for the affected girls, more transparency and full information about the risks of this vaccination to be made available to parents prior to consent. Their aim is also to ensure the MHRA are held to account and made to follow up all reports of serious adverse reactions, which currently does not happen.

Notes:

  1. AHVID recently conducted a member questionnaire and, so far, has received almost 100 responses. Information for the first 94 responses had been already shared with the EMA. Many of the questionnaire responses leave no doubt whatsoever in our opinion that these vaccines have at least contributed to the girls’ side effects.

AHVID has found that in the first 94 questionnaire submissions:

  • Yellow Cards have only been submitted by 13 doctors whilst the girls had been seen by a total of approximately 858 doctors. There were also 7 doctors who refused to raise Yellow Cards.
  • 15 of these had reactions after the 1st and/or 2nd dose. They continued to have the 2nd and 3rd doses because the serious side effects were not perceived to be adverse reactions to the vaccine.  They had all been told that the vaccine is safe and side-effects are only mild and short term.
  • 27 girls had reactions on the same day as the vaccine, some of them within minutes. A further 22 had reactions within 7 days of vaccination and a further 16 within 30 days. This cannot be a coincidence.
  • 66 girls with previously regular periods developed severe problems, many of them serious. 20 girls with irregular periods developed new problems, many of them serious. At least 4 girls have been diagnosed with polycystic ovaries.
  • 53 girls were found to have vitamin and mineral deficiencies with 33 of these being for vitamin D.
  • 24 have confirmed POTS diagnosis, some took 6 and a half years from vaccination to be diagnosed
  • 37 have not been diagnosed with POTS but have an average of 16 typical POTS symptoms. Some had 33 typical POTS symptoms. 19 were refused POTS assessments.
  • 8 have confirmed diagnosis of CRPS.
  • 76 have not been diagnosed with CRPS but have an average of 5 typical CRPS symptoms. 14 were refused CRPS assessments.
  1. Danish reports highlighting estimates of 1 in 400 girls suffering serious adverse reactions:

For further information about AHVID contact: Freda Birrell (chair) at jeanfreda8@btinternet.com or tel: 07752 945545

This article in it’s entirety, is compliments of Sane Vax

HPV Vaccines: Freda Birrell Addresses Scottish Petitions Committee#android#iPad#retweet

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BY  

Freda Birrell

I would like to thank the Committee for allowing me to provide additional information relating to my request for ‘A round table discussion to be held at Edinburgh between scientists and medical professionals from both sides of the HPV vaccine safety debate.’  I speak today on behalf of not only the UK Association for HPV Vaccine Injured Daughters who have had their lives turned upside down after HPV vaccine administration, but each of the 2019 people from 55 countries who signed because they are having similar experiences and support open scientific discussions.

Our association was organized at the beginning of this year when it became apparent that we needed to co-ordinate everyone’s individual efforts as a group. Our association represents families from Scotland, England, Wales and Northern Ireland operating under the banner of HPV Vaccine Injured Daughters (AHVID).  As a group, we were able to receive greater publicity. The increased awareness caused our membership to grow by leaps and bounds. Our initial group of 60 members has expanded to 208 and rising. Despite the fact that Scotland only accounts for 8% of the UK population; 15% of the association’s members come from Scotland. We don’t know how many others are out there, but for now there appears to be no end in sight.

A senior politician within the Irish Government, Pashal Mooney, gave an impassioned plea to Irish Government officials regarding the Irish HPV vaccination program, lack of informed consent and the devastating effects on young girls around the country. He specifically mentions Irish girls being admitted to psychiatric hospitals following HPV vaccinations.

Japan has rescinded the government recommendation for HPV vaccines and initiated studies to determine whether there is a causal relationship between HPV vaccines and adverse outcomes as well as a 21 year study to determine whether HPV vaccines have an impact on cervical cancer diagnosis rates.

  • In Denmark, the National Association of HPV Adverse Sufferers is hosting an HPV Vaccine Information Symposium to bring families together with medical professionals, health authorities and legal professionals to explore treatment options and potential legal remedies on October 31st. Denmark has just recently made the decision to change from Gardasil to Cervarix as the HPV vaccine of choice. 24 Oct 2015, at the urging of Liselott Blixt, Danish politician with a Gardasil injured daughter the Danish government has set aside 7 million kroner to conduct an independent investigation into the HPV vaccine and its side effects.

Our association is in the process of compiling information to submit to the EMA for consideration during their safety assessment of HPV vaccines. Of the 88 family reports analysed to date: 68% reported their daughters experienced health problems serious enough to interfere with their education; 24% reported symptoms so severe their daughter could no longer participate in educational activities; 70% required help with daily care; and a full 91% reported being told their daughters’ medical conditions were psychological in origin.

Psychological in origin? Interesting to note that national health authorities in Denmark, Norway, Japan, France, Spain, Colombia, Ireland, and many other countries have led doctors and other vaccine administrators to believe that any new medical conditions experienced after HPV vaccine administration are most likely psychosomatic. Consequently, when the average medical health professional is faced with a patient exhibiting symptoms they have never seen before; symptoms which do not fit neatly into any current diagnostic criteria, the natural assumption is psychological problems as have been experienced by many UK families.

So, I put forth these facts for your consideration:

  • According to Merck’s Gardasil 9 package insert, 3.3% of participants who were given Gardasil during the most recent clinical trials “experienced new medical conditions potentially indicative of autoimmune disorders.” (3,300/100,000 recipients)
  • According to a press release from Sanofi-Pasteur MSD dated June 17, 2015, 183 million doses of Gardasil have been distributed worldwide.
  • Using Merck’s own clinical trial percentage, this means there could be as many as 6,039,000 girls around the world suffering autoimmune conditions which could very well influence their health for the rest of their lives.
  • According to the World Cancer Research Foundation, there were 528,000 cases of cervical cancer diagnosed worldwide in 2012.

Is this worth the risk? I am very much aware HPV vaccines are a controversial issue and that this information puts Scotland at a cross-roads with a difficult decision to make.

Do we accept what the manufacturer and their list of experts are saying and assume HPV vaccines are safe and effective and there just happens to be an epidemic of psychosomatic disorders spreading round the world affecting certain young people who have one thing in common, they were injected with HPV vaccines?

Or, do we listen to experts from both sides, try to discover exactly what the situation is and make every effort we can to get the problem solved?

Do we sweep all of these families under the proverbial ‘psychological disorder’ carpet and ignore their misery; or do we treat them with the dignity and respect they deserve by using every means at our disposal to identify those at risk of serious adverse reactions and develop successful treatment protocols for those already suffering?

Please, demonstrate to the world that Scotland is still a country that does not ignore the suffering of innocents.

Show the world Scotland is not afraid to hold open, honest scientific discussions no matter how controversial the subject might be.

Witness Freda’s presentation here, beginning at the 1:00:00 mark.

View petition documents, including supporting evidence from medical and scientific professionals here.

Read this presentation in Spanish here.

 

References:

  1. http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM426457.pdf
  2. http://www.multivu.com/players/English/7543051-sanofi-pasteur-gardasil9/
  3. http://www.wcrf.org/int/cancer-facts-figures/worldwide-data

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

Court told of ‘horrendous adverse effects’ of HPV vaccine#android#iPad#retweet

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by Mary Carolan

A mother who claims her daughter suffered “horrendous adverse effects” after receiving the HPV vaccine against cervical cancer has brought legal proceedings.

Fiona Kirby, Kilbeggan, Co Westmeath, is a member of a parents support group, REGRET (Reaction and Effects of Gardasil Resulting in Extreme Trauma), for those who claim their teenage girls became ill after getting the vaccine.

Ms Kirby, a nurse, is seeking a High Court order for the withdrawal of the license given for the Gardasil HPV vaccine, currently being offered to the parents of 11-16 year old girls as a possible cervical cancer preventative.

An order restraining the Health Products Regulatory Authority (HPRA), which monitors health products in Ireland, proceeding with use of Gardasil in any vaccine programme is also sought.

The vaccine has been offered to teenage girls in Ireland since May 2010 as part of the schools vaccination programme and is recommended by the World Health Organsiation.

The REGRET group…

Continue to the Article Here

http://www.irishtimes.com/