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

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.

Gardasil: 5 years to the light at the end of the tunnel?#Vaccines#HPV#Health

By Donna Eliassen, Australia

Part 1 – The nightmare begins:  http://sanevax.org/shania-from-australia/

Part 2 – A promising update:  http://sanevax.org/update-on-shania-the-flyer-mandurah-western-australia/

Shania from Australia

It is now May 2014.  It was May 2009 when Shania had the first of the two Gardasil shots that ruined her swimming career and her life in the ensuing years.  (You can read about that in the links above.)

In 2014, the only obvious legacy from the Gardasil damage is a poor immune system.  But we are working on that.  Other changes…

This year she has been one of the first to catch the seasonal colds but unlike the past years, the colds have not all gone straight to her chest and given her bronchitis; neither have they hung around for weeks or months.  She is bouncing back more quickly, which is a hugely positive sign.  And she no longer needs her Asthma puffer either.

It has been said that the effects of the Gardasil vaccine may only last 5 years and that 5 year limitation is every Gardasil victim’s lifeline.  Here’s why…

It started last year – obvious signs that something was happening healing-wise.  Shania was in 2 major shows one after the other for starters.  She had the lead of Mabel in Gilbert and Sullivan’s ‘Pirates of Penzance’ the first part of the year, and then she went straight into the ensemble of ‘The Phantom of the Opera’ for the second part of the year (her idea of relaxation!).

THIS year, 2014, is her final year (year 12) at Senior High School level in Australia.  (Next year is University.)  This year, the DAY BEFORE THE COMPETITION, the Director of Sports at her college begged and pleaded with her to consider to swim with their relay team at the inter-schools competition, even if she didn’t want to do the individual races, just help them out with the relay events.  Apparently one of the swimmers had to drop out at the last minute.

Of course, she said no.  She’s had to say no every year since 2009. She hasn’t been in the pool racing since she collapsed in 2009. She hasn’t trained since she tried to go back in 2010 and realized she couldn’t.  The mind was willing but the body couldn’t.  And now, she’d been out of the pool 4-5 years and this guy wanted her to race?

But he persisted.  His argument was that even in her poor condition having not swum or trained for so many years, she was still bound to be better than somebody with none of her background.

Cutting a long story short he wore her down.  The College swim team had been training for months and had even gone on a swimming “camp”!  Shania’s only “training” for this event was a 40 minute warm up the night before the competition at the local pool.  I sat on the sidelines, a very worried mum because the last time she’d been in the pool racing was early 2009.

Next day at the competition at Challenge Stadium she swam in the relay team for the B Division of the College.  They put her in first place in this relay team – the first swimmer off the block.  To her and everyone else’s surprise, she gave the team a nice lead and a head start over the schools in the other lanes.

The teachers were so impressed they figured they’d put her in their A Division relay team too.  They placed her second in the team, meaning she’d be the second swimmer off the blocks. A new experience for her – in her past swimming life she had always been either the first swimmer (to give the team a good lead) or the last swimmer (to catch up if the team wasn’t in first place).  But she didn’t care.  She was happy to be back in the pool doing what she loved.

So, the A Division relay starts… The first swimmer went in and at the end of the first 50m leg, their team was in 6th place…  not a great start… better than 7th or 8th, of course, but hardly inspiring for Shania who had to follow this as the second swimmer.

She dove in and started swimming.  She powered up the pool from 6th place, overtaking all the other lanes and when she touched the other end, she’d put her team in first place with a good lead.  The Announcer said “Who on earth is THAT!”

The school sport director was celebrating.  He knew who it was and he’d seen it all before… albeit many years before!

It also heralded the moment when I finally believed that we were no longer in that tunnel looking at the light at the end… we had passed through it!  Shania could not have done what she had if Gardasil was still affecting her. And she couldn’t keep up this timetable either…

This year she is in her final Year 12 of school.  She is studying 5 TEE subjects.  Her homework schedule has to be seen to be believed!  Now she knows why some people only do 3 or 4 TEE subjects… she chose 5.  One of them requires filming on weekends and in her precious holiday breaks – Media…

She is also the College Cultural Prefect with additional responsibilities including having to arrange the Year 12 Ball.  She is also the lead, Belle, in the College musical production of Beauty and the Beast.  She rehearses 2-3 times a week and this includes some Sundays, like tomorrow – from 10 am to 4 pm, and then she comes home and has to knuckle down and do homework and study.

Plus she does a LOT of singing – she has to learn about 7 songs for her exams, plus she recently sang the National Anthem at the Peel region ANZAC Day Memorial Service, and has to rehearse 7 other songs because she is singing at a private soiree later this month.  She let piano go but only because she simply couldn’t fit it in!

Every Saturday morning, we drive up into the city a good hour’s drive away for her classical lessons, then zoom back home and then she goes to work from 1 to 5 at a news agency. Sometimes she goes to a babysitting assignment after that.  She also goes to the gym once or twice a week. She is burning the candle at both ends trying to study for Year 12 exams and all the assignments she has on her plate, often not getting to bed until midnight or after.  In between all this she squeezes in time to see her boyfriend and friends.

Does this sound like someone suffering Gardasil injuries?

Shania had 2 of the 3 Gardasil injections.  I believe if she had had the full 3 shots she would not be here today.  Things were so bad five years ago, I never believed I’d see this day.  Look how far she’s come!

I hope this gives hope to other Gardasil victims that they, too, might also get their lives back eventually… Shania is living proof that it can happen.  It HAS happened.

Donna Eliassen
(Shania’s mum)
 
This article, in it’s entirety, is compliments of SaneVax.org

Spain: First case filed against HPV vaccine manufacturers and health authorities#Vaccines#HPV#Health

By Alicia Capilla (President of AAVP)

AAVP-logo-Spain-smallAAVP, together with law firm Almodóvar & Jara, filed the first of a long series of lawsuits for damages caused by HPV vaccines. The complaint is filed in the High Court against health authorities and vaccine manufacturers.

The process of trying to find justice now begins for one of the Valencian girls who suffered an adverse reaction after the second shot of Gardasil in 2009. Spanish families whose lives have been adversely impacted by HPV vaccines have organized as the Association of Affected People by HPV Vaccine (AAVP www.aavp.es) to assist others in similar circumstances.

The well documented lawsuit is based on violations of the fundamental right to informed consent prior to medical interventions which all citizens have.

Parents whose daughters are vaccinated with Gardasil are not informed beforehand of the possible risks their daughters may suffer, despite the fact there are numerous reports in Spanish, European and American databases. Furthermore, most of the adverse reactions these girls suffered are included in the brochure/leaflet of the product.

The introduction of HPV vaccines into the market without their real effectiveness being known is another issue. The effectiveness has not sufficiently been proven and will not be demonstrated for decades.

Much of the damage these vaccines are producing is being hidden, despite the fact that pharmacovigilance systems around the world are collecting numerous reports of similar reactions.

Moreover, the Spanish Health Ministry withheld information from affected families by denying that the damage the girls suffered was legitimate and previously known via similar cases being reported to health authorities in various countries.

The  Spanish Ministry of Health, Sanofi Pasteur, and Merck, Sharp and Dohme (MSD), producers of Gardasil®, human papillomavirus vaccine, have a responsibility to report accurately and in a timely manner all data available at the time.

Health authorities around the world are trying to deny any causal relationship between HPV vaccines and adverse events occurring after vaccine use. In some cases, authorities say that the new medical conditions are psychological. This is a paradox because if people in different times and different places suffer a similar adverse reaction, it is undeniable that the cause is the vaccine.

The damage these girls have suffered and many continue to suffer were not all included in the leaflet at the time of injection. Some of them were included later. Others continue without being warned.

Based on data that the AAVP has examined, the number of suspected deaths and serious sequelae left behind after human papillomavirus vaccines is completely unacceptable.

As stated in the case filed, health authorities do not investigate the facts and their attitude is favoring manufacturers. They even accused the victims of suffering psychological disorders, which is not true.

This first case will be followed by another four within two months. The firm will continue to file additional cases, not only against Gardasil® but also Cervarix®, the other brand of the HPV vaccinemanufactured by GlaxoSmithKline.

www.aavp.es

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

HPV Vaccine Trials in India: Is Merck above the law?#vaccines#iBelieve#HPV

By Norma Erickson            

3 July 2014: As a result of continued investigations regarding clinical trials involving HPV vaccines in India, more allegations of unethical conduct have been lodged against Merck. These allegations pertain to Merck’s recent trials of the new V503 HPV vaccine, a proposed nine valent HPV vaccine. A complete report of the investigation results written by Dr. Anand Rai, Kelly O’Connor, Amoli Tuli, and Anisha Bhattacharya is now a matter of public record. (Link to report)

The additional allegations of multiple ethics violations were added to a currently ongoing Supreme Court Case via an affidavit added as an addendum to the brief previously prepared regarding the ’demonstration projects’ conducted by a U.S NGO PATH in India beginning in 2009. The deaths of subjects during the ’demonstration projects’ resulted in a government-ordered enquiry and  suspension of all HPV vaccine trials in India pending further investigation. This suspension was effective as of April 2010 and is still in effect.

Ultimately, the suspension and subsequent investigations allowed advocates in India to take their case all the way to the Supreme Court. The petition for the case was formally admitted by the judges on January 7, 2013. By September 2013, the court had issued notices to all participants involved while the Indian Parliament issued a scathing comment condemning all organizations involved in the so-called ’demonstration projects’ calling them a case of child abuse expressly carried out to create a market for the two companies – Merck and GlaxoSmithKline.

According to new allegations, Merck ignored the suspension of HPV-related clinical trials and continued with a phase III trial of the yet-to-be-approved investigational HPV vaccine called V503, which theoretically adds protection against 5 types of HPV to the ones already included in their current HPV vaccine, Gardasil.

Allegations of Merck’s Misconduct

The supplemental affidavit submitted to the Supreme Court of India states that Merck and/or their representatives committed the following violations of basic human rights:

1. Respondent No. 8, MSD Pharmaceuticals Pvt. Ltd.  and its affiliate companies in respect of pre-licensure trials with investigational HPV vaccine V-503.

2. Pre-licensure Phase III trials were carried out at many centres in India. One of these centres was Indore. In Indore this vaccine was administered to 44 children, boys and girls. A field study with the participants was carried out by Dr. Anand Rai and others and is detailed in the Annexure.

3. The timing of this trial was such that vaccination was carried out during the same period when Respondent no. 1, The Ministry of Health and Family Welfare, had asked all HPV related studies to suspend vaccination. As such then this was a violation of the government orders.

4. The Annexure also lists in detail all the problems with this trial on a case by case basis, some of them are summarized below:

a) This clinical trial was not preceded by any trial among adults thereby violating the Drugs and Cosmetics Act. This trial had the approval of the Respondent No. 2, The Drugs Controller General of India (DCGI), who violated the law that his job specifically asked him to uphold. The petitioners have complained to the court that is the second time regarding HPV vaccines the DCGI bestowed this favour on Merck and its associates.

b) The trial used middle men and women acting as agents of the investigator who went around residential areas recruiting subjects in complete violation of all national and international guidelines.

c) The trial was carried out at a government hospital using government stationery and seal even though this was a privately sponsored trial of the company thereby misusing the trust parents place in the governmental vaccination programmes.

d) The parents and children were told that they were getting a successful vaccine from abroad free which would otherwise cost Rs 10,000. This was a blatant lie as this vaccine was not approved for marketing anywhere in the world. Also this constituted undue inducement to recruit children to this trial.

e) None of the participants were informed that they were participating in a clinical trial.

f) Economically vulnerable sections and those from scheduled castes and minorities were recruited for the trial, those who would not be able to afford the vaccine if and when it is marketed; thereby the trial further violated all laws and guidelines in this regard.

g) Merck listed history of allergic reaction that required medical intervention, currently enrolled in another clinical trial, subject is pregnant, subject is immunocompromised or has taken immunosuppressants in the last year, subject has received a marketed HPV vaccine or participated in an HPV vaccine clinical trial and subject has history of positive test for HPV as exclusion criteria for this clinical trial. No examinations of the children who were selected for participation were undertaken prior to administration of the V503 vaccine.

h) There was no placebo involved in this trial, simply three different lots of V503, despite the fact that one purpose of the trials was to detect potential safety issues.

i) From the beginning to end, there was no examination of the children for their health status, and even though the trial was supposedly carried out to determine the safety of the vaccine not even fever post vaccination was recorded.

j) No medical care was provided for the health problems of the children nor were they provided any compensation. The study found many children who continue to suffer new medical problems even as late as 2013. Out of the 12 individuals interviewed, 4 have experienced health problems after the vaccine, such as mood swings, persistent stomach aches, dizziness, late onset of periods and severe anaemia. One boy whose family was interviewed has suffered extreme weight loss.

k) Though the investigation covered only the trial centre at Indore the entire list of trial centres is placed in the supplemental affidavit for information. In all hundreds of children have been affected in India.

One would think all of the complaints filed against PATH and Merck during the ’demonstration projects’ for Gardasil would have caused them to be on their best behavior. But apparently, when the government officials in India called a halt to any trials relating to HPV, Merck thought the decree did not apply to them. Either that, or they believed themselves powerful enough to be above the law.

Whatever the motivation, it appears hundreds more economically disadvantaged children and their families were put at risk by their participation in a clinical trial they were not told they were taking part in.

Compound this disregard for informed consent with participants being told they were priviledged to receive a successful and very expensive vaccine from overseas. Nevermind the fact that this ’successful vaccine’ had not been approved for use in any country in the world.

The people of India are not the only ones who may suffer the effects of this particular set of clinical trials. What ’results’ will Merck report to the rest of the world on this set of trials where the exclusion criteria was apparently ignored?

What ’results’ will Merck report to the rest of the world when no adverse events were recorded? One can certainly assume the adverse events which apparently were not recorded will no longer exist.

Will pretending these new medical conditions did not happen allow Merck to report their new V503 HPV vaccine is safe?

Is Merck above the law?

Will Merck be allowed to ignore the international laws protecting the basic right of informed consent prior to participation in clinical trials? Will Merck be allowed to continue to exploit economically disadvantaged people then extrapolate the resulting ’conclusions’ to the entire population of the world?

One can only hope the Supreme Court in India decides to protect the health and well-being of their young people by responding to the complaints of the organizations who put forth the allegations in a manner which will stop these types of abuses from ever happening in their country again.

By doing so, India’s Supreme Court Judges could help protect all of the world’s young people.

The Supreme Court of India has scheduled the final hearing of this case for August 12, 2014. The Court’s decision should be rendered on that date.

Whatever the ultimate outcome, advocates around the world will be watching.

Article in it’s entirety, compliments of SaneVax.org

Show Me The Science#vaccines#Health#iBelieve

We have compiled this catalogue of science to help parents, lawmakers, medical practitioners and scientists understand several important points about the vaccine issue:

  • there is abundant science published in mainstream medical and scientific journals suggesting cause for concern about the safety of vaccines;
  • the vaccine debate is not a debate between parents and doctors but rather amongst scientists with opposing views;
  • vaccines may be linked to a host of chronic illnesses and conditions such as asthma, allergies, learning disabilities, behavioral problems, autism, unexplained infant death and autoimmune diseases such as diabetes, rheumatoid arthritis, lupus, MS, and others;
  • there are connections between the gut, immune, and neurological issues often seen in vaccine injuries.

Science Catalogue continued here

greatergoodmovie.org

Is The Epidemic of Sudden Infant Deaths A Medically Induced ‘Syndrome’?#vaccines#iBelieve#Health

A new study published in Current Medicine and Chemistry titled, “Sudden infant death following hexavalent vaccination: a neuropathologic study,” lends support for the long theorized link between an ever-expanding number of infant vaccines and Sudden Infant Death Syndrome (SIDS).

The fact that the peak age for SIDS is 2–4 months, which coincides with the introduction of 11 shots containing 16 vaccines (within the US immunization schedule), is so obvious a cause for concern, that even the CDC has been compelled to address the seeming ‘coincidence’ directly:

“From 2 to 4 months old, babies begin their primary course of vaccinations. This is also the peak age for sudden infant death syndrome (SIDS). The timing of these two events has led some people to believe they might be related…With babies receiving multiple doses of vaccines during their first year of life and SIDS being the leading cause of death in babies between one month and one year of age, CDC has led research studies to look for possible linkage.”

Unsurprisingly, the CDC, whose pro-vaccine agenda is glaringly oblivious to the 100+ documented serious, unintended adverse effects of vaccines as evidenced in the biomedical literature, claims extensive research they commissioned has found vaccines do not cause SIDS. Despite the CDC’s dismissal, infant mortality rates are highest among countries that administer the most vaccines within the most vulnerable developmental window of infanthood. A 2011 study published in Human & Experimental Toxicology, for instance, observed that “The US childhood immunization schedule specifies 26 vaccine doses for infants aged less than 1 year—the most in the world—yet 33 nations have lower IMRs [infant mortality rates].” They found that across the 34 nations analyzed “a high statistically significant correlation between increasing number of vaccine doses and increasing infant mortality rates, with r = 0.992 (p = 0.0009).”

Also, a recent study published in Vaccine titled, “Co-administration of live measles and yellow fever vaccines and inactivated pentavalent vaccines is associated with increased mortality compared with measles and yellow fever vaccines only” found multiple infant vaccines dramatically increased the risk of mortality in a trial conducted in the West African country of Guinea-Bissau…

Continue to article here

greenmedinfo.com

HPV Vaccines: Time for Science#iBelieve#vaccines#HPV

SaneVax-Featured

 

By Norma Erickson

According to the World Health Organization (WHO), as of January 2014 fifty-two countries have included HPV vaccines, either Gardasil or Cervarix, in their national immunization programs. During the last five years, the SaneVax Team has been contacted by representatives from 24 of those countries who are seeking to understand the vast array of new medical conditions occurring in the wake of these programs.

1.2014-WHO-Countries-with-National-HPV-Vax-programs(Note: SaneVax has been contacted by multiple people in Australia, Argentina, Belgium, Canada, Colombia, Denmark, Finland, France, Germany, India, Ireland, Israel, Japan, Malaysia, Morocco,  New Zealand, Norway, Peru, Scotland, Spain, Sweden, Switzerland, the United Kingdom and the United States – all requesting further information on HPV vaccines and vaccination programs.)

Why would so many countries contact an organization dedicated to the promotion of only safe, affordable, necessary and effective vaccines and vaccination programs in such a relatively short period of time? Let’s take a look at the science.

In 2006, when the FDA approved the first HPV vaccine (Gardasil) for cervical cancer prevention they should have known that HPV does not cause cervical cancer without other risk factors being involved. They should have known that the endpoints chosen to evaluate the efficacy of the vaccine were not sufficient to prove future cervical cancer prevention because ASCUS and CIN1/2/3 frequently resolve on their own, or can be detected by currently available tests (pap smears) and treated safely and effectively prior to progression to cervical cancer. They should have known that allowing the manufacturer to use a reactive aluminum adjuvant as a ’control solution’instead of an inert placebo could potentially mask adverse effects making the vaccine appear more safe than it actually is.

Any one of these facts should have raised questions about the practicality of utilizing HPV vaccines in any cervical cancer prevention program. Apparently the facts above were either not known, or they were ignored. Gardasil was awarded fast-track approval despite the fact there was no cervical cancer crisis in the United States. A short time later, Cervarix was approved for the same indication.

Since health officials at the FDA are apparently ignoring scientific facts medical consumers need to be aware of the science, or lack therof, behind HPV vaccines.

Does HPV cause cervical cancer?

HPV-real-risk-GSKAccording to WHO, only 0.15% of people exposed to any high risk HPV types will ever develop cervical cancer. We do not have a publication date on the chart to the right, so let’s assume this is new knowledge, information which the FDA officials responsible for the fast-track approval of Gardasil did not have when they made the decision to approve the vaccines for cervical cancer prevention.

Medical consumers need to know that according to the World Health Organization 99.85% of those exposed to oncogenic types of HPV will never develop cervical cancer.

IF the FDA did not know this prior to approving HPV vaccines to ’prevent’ cervical cancer, they are most assuredly know it now. Consider the following quote from an FDA/CBER (Center for Biologics Evaluation and Research) meeting held on September 19, 2012 to discuss the use of human tumor cells in vaccine production (verify on pages 91-92 of this transcript):

“However, even tumor induction by acute oncogenic viruses requires additional oncogenic events. The best example is the Human Papillomavirus, where even infection with a high risk of Papillomavirus types is not sufficient to induce cervical cancer. Mutation in other genes and perhaps also epigenetic events are required. If a single infection-induced cervical cancer after infection with HPV, say, 16, then teenagers will be getting cervical cancer. And as we know, cervical cancer is a disease of older people”.

So, there you have it – even infection with a high risk strain of papillomavirus types is not sufficient to induce cervical cancer. Since at least September 2012, FDA officials knew infections with high-risk HPV types will not induce cancer without genetic mutations and/or other epigenetic (relating to or arising from nongenetic influences on gene expression) events occurring also.

Did this cause the FDA or CDC to re-examine the usefulness of HPV vaccines? No.

Were clinical trial endpoints valid?

Prior to the marketing push for HPV vaccines, CIN1/2/3 were known as abnormal cells – something that needed to be observed until treatment was required. Now, they are almost always referred to as ‘pre-cancerous’ lesions. This serves no purpose other than to strike fear into the heart of almost any woman on the face of the planet. The nature of the abnormal cells has not changed, simply the terminology. No mention is made of the fact that CIN1, CIN2 and often CIN3 abnormal cells revert to normal cells without medical intervention.

Not many people are aware of the fact that most CIN1 lesions go away on their own within two years. 25-50% of CIN2 lesions regress on their own within the same two year time frame. According to the International Agency for Research on Cancer (IARC), World Health Organization, the results of a pooled analysis of studies published between 1950 and 1993 indicated only 12% of CIN3 lesions progress to invasive cervical cancer.

Consider the following quote from Chapter 2 of the IARC’s COLPOSCOPY AND TREATMENT OF CERVICAL INTRAEPITHELIAL NEOPLASIA: A BEGINNER’S MANUAL states:

“Despite women’s frequent exposure to HPV, development of cervical neoplasia is uncommon. Most cervical abnormalities caused by HPV infection are unlikely to progress to high-grade CIN or cervical cancer, as most of them regress by themselves. The long time frame between initial infection and overt disease indicates that several cofactors (e.g., genetic differences, hormonal effects, micronutrient deficiencies, smoking, or chronic inflammation) may be necessary for disease progression. Spontaneous regression of CIN may also indicate that many women may not be exposed to these cofactors.”

Please note this manual was designed to teach medical and nursing personnel in developing countries where diagnostic and therapeutic expertise is not readily available. In other words, the progression from HPV exposure to potential development of cervical cancer is similar in both developing countries and developed countries. It also indicates that several cofactors (risk factors) may be needed for HPV exposure to progress to abnormal lesions, much less cervical cancer.

Surely, FDA officials were aware of the information contained in a beginner’s manual to treatment of so-called ‘precancerous’ lesions published by the World Health Organization. If not, they certainly should have been. Nevertheless, they allowed these very same abnormal cells which typically revert to normal on their own to be used to evaluate the efficacy of HPV vaccines against cervical cancer.

Medical consumers need to know, according to WHO only 1% of CIN1, 1.5% of CIN2 and 12% of CIN3 progress to invasive cervical cancer. This is in developing countries. In countries where pap smears are routinely administered the percentages should be much lower. Could using these abnormal cells as endpoints in clinical trials artificially inflate the predicted efficacy of HPV vaccines against cervical cancer? Absolutely!

Why not use a true placebo during clinical trials?

When conducting scientific experiments to evaluate a new substance, standard practice is to have at least two groups – one group using the substance being examined and the other using a placebo. This way, the scientific team can evaluate the effects and safety of the new substance by comparing both groups’ results at the end of the study.

The definition of placebo is “a substance having no pharmacological effect, but administered as a control in testing experimentally or clinically the efficacy of a biologically active preparation.”

There is no doubt about vaccines being a biologically active preparation. But, how about aluminum – one of the major ingredients in the proprietary AAHS solution which Merck was allowed to use as a control solution in the vast majority of clinical trials for Gardasil?

A quick search of PubMed, using the terms ‘aluminum toxicity human’ returns 1620 papers on studies conducted as early as 1966. If you narrow the search to ‘injected aluminum toxicity’ you come up with 116 papers published as early as 1974. Refine the search even further to ‘injected aluminum toxicity human’ and you still get 31 scientific papers published between 1979 and 2014.

It is extremely difficult to believe the FDA officials responsible for reviewing Gardasil’s application for approval did not know that aluminum compounds were potentially toxic to humans. Yet, they accepted the use of a proprietary (meaning no one knows what was included other than aluminum) AAHS aluminum adjuvant as a control solution instead of an inert placebo.

FDA officials knew, or should have known, that clinical trials conducted in this manner proved nothing other than the fact that Gardasil was no less dangerous than the new AAHS adjuvant which had never been tested for safety in humans. FDA officials ignored the fact that over 70% of all clinical trial participants reported new medical conditions after the trials. (Verify here) One can only speculate as to why this fact did not raise a huge red flag, but apparently it did not.

The FDA could certainly not use the excuse that it would be unethical to withhold vaccination from any of the clinical trial participants because there was currently no ‘comparable’ vaccine available. Why then, did they not require a real placebo?

Is the FDA ignoring new scientific evidence?

Below is a list of scientific information presented to government health officials around the world. None of the presentations below have brought forth a response from FDA officials. Please keep in mind this is by no means a complete list; it is simply a sample:

How long are medical consumers supposed to put their faith in an agency that repeatedly ignores standard scientific methodology, not to mention scientific evidence? Medical consumers need to remember every single medication that has ever been pulled from the market was first approved ‘safe and effective’ by the FDA. Can you trust them with your life?

Remember – Research before Consent – you can’t un-vaccinate.

Article compliments of SaneVax.org

Spotlight on Gardasil in France#Vaccines#HPV#iBelieve

SaneVax-Featured

By Helen Kimball-Brooke MARH, guest author

A press conference on the Gardasil vaccine was held in Paris on Wednesday the 2nd April 2014 at the local offices of the European Parliament, a short walk from the French National Assembly.  It was organised by MEP Michèle Rivasi (Vice-Chair of the Greens/European Free Alliance group) who has held meetings in the past on pharmacovigilance in Brussels and other press conferences on the aluminium salts used as adjuvants in vaccines, in Paris.  Three members of EFVV (the European Forum for Vaccine Vigilance) attended the conference: myself, Françoise Joët from the French group ALIS and Dr. Françoise Berthoud, retired homeopathic paediatrician from Switzerland.

French Press Conference

Aside from Michèle Rivasi, the speakers included the parents of two HPV-vaccine victims: 18-year-old Marie-Océane Bourguignon who after receiving two doses of Gardasil at age 15 now suffers from multiple sclerosis (MS) and Orianne Lochu, age 21, a former first-year medical student now struggling with severe macrophagic myofasciitis, an illness thought to be linked with the aluminium adjuvants in vaccines.  Both HPV vaccines, Gardasil and Cervarix, contain aluminium salts.  Within months of her jabs, Océane, the only French HPV vaccine victim for whom the link to the vaccine has been officially recognised by a Medicine Injury court, temporarily lost both her sight and the use of her legs after being hospitalised for what appeared to be either acute disseminated encephalomyelitis (ADEM) or multiple sclerosis.

Océane’s case was originally heard by the Bordeaux Commission de Conciliation et d’Indemnisation or Medical Accident Arbitration and Compensation Committee, set up by the Ministry of Justice with members appointed by the local Public Health Authority.  As of the judgement in September 2013 she was awarded compensation amounting to 50% of her claim but given that Sanofi-Pasteur were clearly incriminated in the case and thinking of all the other victims, her parents chose to forfeit the compensation by filing charges in the criminal courts.  The criminal court case is still pending.

The parents of both girls expressed anger and frustration over the way they had been treated: refusal by the medical profession to acknowledge that their daughters’ illnesses had been triggered by the vaccine, lack of support and treatment for the girls’ ailments, even suspicion and ostracism for having dared to blame the vaccine.  The experience has been all the more difficult for Orianne’s parents who are medical professionals themselves: her father is an anaesthesiologist and her mother a nurse.

Océane’s lawyer, Maître Jean-Christophe Coubris, also defending over 100 other French HPV-vaccine victims, was another speaker, as was Serge Rader, a pharmacist who has done research on the widely varying prices of vaccines across Europe, and Elena Pasca, a philosopher, member of the board of Sciences Citoyennes and author of a blog called Pharmacritique, who discussed the conflicts of interest inherent in the development and marketing of these vaccines.

Others present included French medical consultants Profs. Authier and Gherardi, doing research on the aluminium salt adjuvants in vaccines at the Henri-Mondor Hospital in Créteil, a Parisian suburb, and consultant Dr. Laurent Belec, head of the virology laboratory at the Georges Pompidou European Hospital in Paris.  The sudden withdrawal in 2013 of the funding for the important work of Authier and Gherardi was the topic of another press conference organised by Michèle Rivasi last year.  Their funding was only re-instated after two members of the NGO victim support group E3M went on a hunger strike.

Professor Christopher Shaw

The speakers of honour however were Drs. Christopher Shaw, neurologist, and Lucija Tomljenovic, PhD, from the University of British Columbia, Canada, known for their research on Gardasil and the dangers of its adjuvants.  Currently doing research with Professor Yehuda Shoenfeld in Tel Aviv, Israel, on vaccine adjuvant-induced autoimmune diseases, they spoke of the effects on the body of the aluminium in vaccines.  It has been shown that aluminium migrates through the body to the brain, where it accumulates, potentially causing many adverse effects: convulsions, fainting spells, Guillain-Barré syndrome, transverse myelitis, facial paralysis, chronic fatigue syndrome, autoimmune diseases, pulmonary embolisms, macrophagic myofasciitis, pancreatitis and even death.

Lucija Tomljenovic

 Dr. Tomljenovic demonstrated how these vaccines were rushed prematurely to market.  In the USA, the FDA approved the vaccine very fast, reflecting, in her opinion, the flaws and incompetence which are now sadly a characteristic of the organisation.  Development of cervical cancer from HPV infection is in fact very slow and 90% of HPV infections resolve of their own accord within three years.  The duration of follow-up in the clinical trials was only 4.5 years for Gardasil and 8.4 years for Cervarix but given the slow growth of these cancers, at least 15 if not 20 years would really be needed to establish accurate efficacy. The manufacturers have nonetheless claimed 70% efficacy based on these short-term trials, and Sanofi-Pasteur, who market Gardasil for its manufacturer Merck, have even claimed ‘up to 100%’ efficacy while true vaccine efficacy could be as low as 16.9%.

STIKO, the German Standing Vaccine Committee’s flawed assumption that the vaccine would confer lifelong protection of 92.5% led to the decision to reimburse the HPV vaccine in Germany and incited many German doctors to recommend it.  Since its introduction 7 years ago, nearly 2 million young French women between the ages of 13 and 26 have received at least one dose of Gardasil, reimbursed at 65% by the Social Security, even though its effectiveness has not yet been proven and is highly controversial.  There are in fact over 100 strains of HPV but Gardasil contains only antigens from strains 6, 11, 16 and 18, considered the most oncogenic.  Strains 16 and 18 are responsible for 70% of cervical cancers which is why these are the only two in Cervarix but infections with these two strains also seem to be less common in Europe.  In fact, cervical cancer represents only 1.7% of all cancers in France so it is not actually a public health problem there anymore.

On the 4th of February 2014 however, President François Hollande announced that as part of his ‘Cancer Plan’, he wanted HPV vaccine uptake amongst young French women to double over the next five years.  This came as an enormous shock to the parents of the 10 girls with very severe neurological complaints, who by November 2013 had already initiated legal proceedings against both Sanofi Pasteur and ANSM, the French national medicines safety authority.

To quote Dr. Tomljenovic:

‘Just as pizza-bearing cheerleader drug reps are a poor substitute for medical education, pharmaceutical lobbying is a poor substitute for well-reasoned public health policy-making….Is it ethical to put young women at risk of death or a disabling autoimmune neurodegenerative disease at a pre-adolescent age for a vaccine that has not yet prevented a single case of cervical cancer, a disease that may develop 20-30 years after exposure to HPV, when the same can be prevented with regular Pap screening which carries no risk?’

The number of HPV vaccine victims continues to grow in France and worldwide, with some countries taking a more cautious stance: Austria refused from the start to include the HPV vaccine in its vaccination schedule and during 2013, under pressure from victims, the Japanese Ministry of Health, Labour and Welfare withdrew its recommendation for the HPV vaccine.  Shortly after the press conference in Paris, it was announced in Japan that instead of reinstating the HPV vaccine recommendation, the authorities would hold off for at least another year.

On the 30th March, only three days before the press conference, it was reported in French newspaper Journal du Dimanche that 420 French doctors plus nearly another 300 pharmacists, midwives and other medical professionals had signed a petition demanding a parliamentary mission to reassess Gardasil, claiming that its effectiveness is limited (only 20% according to clinical trials) and its cost exorbitant. They also fear that the vaccine may mislead women into thinking that a Pap smear, whose effectiveness has been proven, is not necessary.  As of late May 2014, there were nearly 1200 signatures on the petition.

Of course a counter-petition was also launched by seven scholarly medical groups affirming the benefits of the vaccine but speaking of cost: what in fact is the actual cost of this HPV vaccine campaign in France?  Mr. Rader informed us that a single dose of Gardasil costs €123.44, compared with prices ranging from €6.50 to €57 for other French vaccines, the prices of which have increased as new vaccines were introduced over the years.  The three jabs required would therefore come to a whopping total cost of €370.32 per individual.  The duration of protection conferred by the initial vaccination is still not known so the overall cost would increase if boosters were required.  A ‘catch-up’ period could generate a cost to the French Social Security of a shocking €926 million and in subsequent years, the annual cost would be €148 million.  What incites more questions however is that a single dose of Gardasil costs only €60.50 in Italy and the Rotavirus vaccine recently recommended for all new-borns by the French High Council for Public Health, costs €54.60 per dose, including tax, compared with only $1 per dose in India.  Why do vaccines cost so much in France?

Pap smears, costing €15.40 each in France, remain the best and most effective way to fight cervical cancer.  The speakers therefore questioned why the French government was so intent on pushing Gardasil whose effectiveness is debateable and will not be known for 15 or more years, let alone its excessive cost.  An indecent communication campaign with lobbying and aggressive advertising was apparently engaged a number of years ago to promote this vaccine.  The adverts played on the fears and guilt especially of mothers and in 2010, one of them was even banned for ‘lack of objectivity’ by the French Medicines Agency.

Mme. Rivasi therefore concluded the press conference with a forceful:

‘Enough is enough!  It is time to demand a moratorium on this vaccine!   EU member states must stop recommending this vaccine until more studies are conducted on Gardasil, its effectiveness and its dangers.’

Michele Rivasi, MEP

Less than two months later, her efforts seemed finally to be having some effect: on the 22nd May, under pressure from victim support groups, primarily E3M, an NGO supporting patients with macrophagic myofasciitis, two colloquia with round-table debates open to the public and in the presence of the press, television and even French Health Minister Marisol Touraine, were organised at the French National Assembly: one in the morning by E3M and facilitated by journalist Viginie Belle, the other in the afternoon by Office parlementaire des choix scientifiques et technologiques (Opecst, similar to our House of Commons Science and Technology Committee).

A fair number of the speakers from the April press conference (Gherardi, Authier, Shoenfeld, Orianne Lochu’s mother, Tomljenovic, Belec, Rivasi) took part, alongside representatives from Sanofi-Pasteur, GSK, the French government and other scientists promoting vaccines.  Pro-caution and pro-choice scientists also included our own Prof. Christopher Exley from Keele University, Dr. Lluis Lujan, veterinary pathologist from the University of Zaragoza in Spain and Prof. Michel Georget, French biologist and author of books on the adverse effects of vaccines.

Topics of the four round-table debates: 1) Aluminium: Adjuvant under Scrutiny. 2) HPV Vaccine: Time to Exercise Caution, in the morning.  Then in the afternoon: 1) The Safety and Efficacy of Aluminium Vaccine Adjuvants.  2.a) Is a Moratorium Appropriate?  2.b) Are there Alternative Vaccine Adjuvants?

For those who speak French, these debates can be viewed here: http://videos.assemblee-nationale.fr/video.5464.  Compared with our House of Commons Science and Technology Committee’s Evidence Check into Homeopathy in 2009, this series of debates seemed far more balanced!  The focus in France seems at present to be only on aluminium, which may not be the only issue but time will tell as to where it takes the whole French and European vaccine debate.

Knowing that the French Health Minister attended these colloquia and is therefore now fully aware of the latest research on the damage caused by aluminium adjuvants and the Gardasil vaccine, it came as a shock when instead of calling for a moratorium she later reaffirmed the French government’s intent to vaccinate all young French women with this vaccine.  Yet another debate was then organised on the 23rd of June by a group of galvanised GPs from La Réunion island, one of France’s overseas departments.  The thrust of this series of medical and statistical presentations, again hosted by Michèle Rivasi, was that HPV vaccination is not needed to prevent cervical cancer, is excessively costly and the whole vaccine development and marketing process is fraught with conflicts of interest.  Gardasil is clearly a hot topic in France with articles, blogs, petitions and debates appearing frequently.  The doctors, researchers, support groups and victims behind these are not about to give up the fight for both a moratorium on Gardasil and aluminium-free vaccines in general.

Remember that in the USA and the UK, HPV and other vaccine victims are fortunate to have SaneVax (http://www.sanevax.org) who in addition to providing the necessary information for making an informed choice, can locate appropriate medical/legal assistance in the event of an adverse event post-vaccination.

Since the April press conference, the EFVV has prepared a Manifesto in English, French, Spanish, Italian, German, Dutch and Slovenian (other languages possibly to follow), demanding the abolition of mandatory vaccination in the EU (see http://www.efvv.eu).  The plan is to launch a petition based on this Manifesto and a delegation of EFVV members will be meeting with Michèle Rivasi in September to discuss the best way to utilise these documents and submit their demands to the European Parliament.  Watch this space, both in France and Europe-wide.

(Note: This article was originally written for Homeopathy in Practice, the journal of the Alliance of Registered Homeopaths in the UK but, with kind permission of HIP, is appearing here first.)

Article compliments of SaneVax.org