France: Permanent Injury Attributed to Gardasil#Vaccines#HPV#Health

By Norma Erickson

Bordeaux: On September 18, 2013, Judge Patrick Mairé handed down a decision stating Gardasil was 50% responsible for the permanent injury of a French teenager who had received two injections of the HPV vaccine. The other 50% was attributed to a genetic pre-disposition for autoimmune disorders. Judge Mairé presides over lawsuits filed with a regional branch of the CRCI in France, which is the equivalent of the Vaccine Injury Compensation Program (VICP) court in the United States.

Gardasil changed my life

Marie –Océane’s parents, Jean-Jacques and Yveline Bourguignon, have granted permission for their daughter’s story to be published hoping they can help make people aware of the potential risks involved with HPV vaccinations. They do not want anyone else to go through what they have experienced without knowing of the possibility in advance.

In 2010, Marie-Océane Bourguignon, age 15, received two injections of Gardasil® the first on October 11th and the second on December 13th. Two weeks after the first injection, she experienced sensory and motor problems in the upper limbs, lasting approximately two weeks before spontaneously and gradually regressing.

Three months after the second injection, on the 13th of March 2011, Mlle. Bourguignon was hospitalized at Centre Hospitalier de Dax for deterioration in her general health, cerebral-vestibular disturbances and sensory-motor impairment (ataxia, vertigo). On March 15, 2011, an MRI of her brain revealed lesions in the white matter.

The initial diagnosis was that she was suffering from either multiple sclerosis or acute disseminated encephalomyelitis (ADEM). After multiple subsequent hospitalizations, it was determined that Marie  had developed multiple sclerosis, a chronic, typically progressive disease involving damage to the sheaths of nerve cells in the brain and spinal cord, whose symptoms may include numbness, impairment of speech and of muscular coordination, blurred vision, and severe fatigue. Marie-Océane will live with this condition for the rest of her life.

Consequently, her parents filed for compensation on her behalf with CRCI, Regional Medical Injury Arbitration and Compensation Tribunal in Bordeaux on January 28, 2012. The decision was handed down on September 18, 2013.

The decision handed down by Judge Mairé was kindly translated into English by Helen Kimball-Brooke and is printed below in its entirety. The Bourguignon family had been successful. They could have accepted the compensation award from the French vaccine compensation program and gone on to live their lives.

But this family knew they were not the only ones to have had their lives turned upside down after using the HPV vaccine, Gardasil. They knew that the decision by CRCI would not be widely publicized in order to warn other families about the potential risks involved with the use of HPV vaccines.

Consequently, they decided to turn down the award and take their case to a traditional criminal court where the outcome of the adjudication could be made public. They decided that a just decision for their family was simply not good enough. They wanted justice for all victims of adverse events after Gardasil. They wanted to have the opportunity to warn others about the potential risks involved with consenting to the use of HPV vaccines. They wanted the opportunity to let the public be aware of the fact that HPV vaccines can be quite dangerous for some individuals.

The Decision Handed Down by the French Vaccine Injury Court:

CRCI

REGIONAL MEDICAL INJURY

ARBITRATION AND COMPENSATION

TRIBUNAL 

NOTICE

(Article L.1142-8 of the French Public Health Code)

Case:           Marie-Océane Bourguignon

File Number:          12.033.C.000071

THE AQUITAINE REGION MEDICAL INJURY, IATROGENIC AILMENT AND NOSOCOMIAL INFECTION ARBITRATION AND COMPENSATION TRIBUNAL, HELD IN BORDEAUX ON THE 18TH SEPTEMBER 2013 AND FORMED TO REACH AN AMICABLE SETTLEMENT

  • Considering the French public health code, articles L. 1142-1 to L. 1142-24, D. 1142-1 to D. 1142-3 and R. 1142-13 to R. 1142-18 in particular; modified French Law no. 2002-303 of the 4th March 2002, regarding patients’ rights and the quality of the health system; also considering the French Order of the 4th March 2003 regarding the documentary evidence to be included in a compensation request lodged with a regional medical injury, iatrogenic ailment and nosocomial infection arbitration and compensation tribunal,
  • Considering the compensation request lodged with the secretariat of the Tribunal on the 28th of January 2012 and deemed to be complete the same day, by Mr. Jean-Jacques Bourguignon and Mrs. Yveline Bourguignon, née Cazaux, acting as the legal representatives for their daughter Marie-Océane Bourguignon, born on the 10th of June 1995, a claim then renewed on the 26th of July 2013 in the names of Mme. Marie-Océane Bourguignon and as indirect victims, Mr. and Mrs. Bourguignon, who are hereby suing:

–        Dr. Fabienne Chatelet

–        SNC Sanofi-Pasteur MSD, 8 rue Jonas Salk, 69007, Lyon 07, insured by Marsh S.A.

  • Considering the various items of evidence included in the file,
  • Considering that Dr. François Rouanet, neurologist, and Dr. Larbi Benali, medical examiner, specialist in compensation for injury, had been appointed by the presiding judge as co-examiners on the 31st of May 2012,
  • Considering the medical examination report submitted on the 26th of June 2013,
  • Considering the statement submitted by Attorney Coubris on behalf of Mr. and Mrs. Bourguignon,
  • Considering the statement submitted by Attorney Annie Berland on behalf of Dr. Chatelet,
  • Considering the statement submitted by Attorney Cécile Derycke on behalf of Sanofi-Pasteur,

Considering the following which was presented during the hearing

The case presentation report by Judge Patrick Mairé, presiding judge, the reports by Drs. Rouanet and Benali, along with the observations made by Attorney Coubris representing Mlle. Océane Bourguignon and her parents, Attorney Annie Berland representing Dr. Chatelet and Attorney Cécile Derycke representing Sanofi-Pasteur.

The tribunal pronounced on:

1.  The circumstances

In 2010, Marie-Océane Bourguignon, age 15 at the time, received two injections of Gardasil ®, a vaccine used to prevent cervical cancer, the first on the 11th of October and the second on the 13th of December that year.  The vaccines were administered by her regular doctor, Dr. Fabienne Chatelet.

Two weeks after the first injection, she experienced sensory and motor problems in the upper limbs, lasting approximately two weeks before spontaneously and gradually regressing.

Three months after the second injection, on the 13th of March 2011, Mlle. Bourguignon was hospitalized at Centre Hospitalier de Dax, the main hospital in Dax, France, for deterioration in her general health, cerebral-vestibular disturbances and sensory-motor impairment (ataxia, vertigo).

She was successfully treated with steroids.

An MRI of the brain was performed on the 15th of March 2011 and revealed lesions in the white matter.

The initial diagnosis was that she was suffering from either multiple sclerosis or acute disseminated encephalomyelitis (ADEM).

Mlle. Bourguignon was later hospitalized on several occasions for the same cerebral-vestibular episodes and progressive flare-ups of inflammation until multiple sclerosis was finally diagnosed after she responded well to treatment with Tysabri ®.

On the day of the medical examination, Mlle. Bourguignon had not recovered her health due to the progressive nature of her pathology.

Mlle. Bourguignon does not display any neurological deficiency or functional disability but she is unable to walk more than 1 km.  She takes mild analgesics for headaches and abdominal pains.  She complains that she has difficulty concentrating and suffers from vertigo.

She feels that Sanofi Pasteur MSD should compensate her for the injury sustained which she attributes to the two injections of Gardasil ® she received.

2.  On the Jurisdiction: 

Considering that Mlle. Bourguignon’s illness restricts her to life-long clinical and radiological supervision as well as a constant feeling of anxiety regarding the expected course of her disease, it is clear that Mlle. Bourguignon experiences particularly serious deterioration in her quality of life, including financial problems, and this justifies the jurisdiction of the tribunal.

3.  On the Substance: 

3.1. Responsibility of Dr. Chatelet

It is clear from the two medical examination reports and the information which the examiners provided to the tribunal that before administering the second injection, Dr. Chatelet performed a full clinical examination of Mlle. Bourguignon and did not observe any residual neurological disorder from the reaction which occurred immediately after the first injection.  She could legitimately have attributed these sensory and motor disorders to an epicondylitis, particularly since the vaccine package insert did not include any mention of the type of reaction her patient had displayed.

There are therefore no grounds for claiming that she is responsible for any fault especially as the plaintiff does not reproach her for anything.

3.2.  Responsibility of Sanofi-Pasteur

The two medical examiners were unable to agree on the diagnosis of the first inflammatory episode so they submitted their reports separately.  Dr. Rouanet felt that it was not possible to specify with certainty whether the first episode could be attributed to a flare-up of multiple sclerosis or to acute disseminated encephalomyelitis (ADEM).  Dr. Benali on the other hand felt that the first episode was a kind of pediatric ADEM.  Aside from the failure to agree on this point, which had no medical or legal impact on the case, the two medical examiners did agree on the fact that this first episode represented the beginning of a vaccine-induced neurological demyelinating inflammatory cascade.

They both concluded categorically that the neurological disorders presented by Mlle Bourguignon had been triggered by the immune decompensation of an unknown prior condition, a decompensation secondary to the vaccination process which led to the initial vaccine-induced acute demyelination, the prodromal physio-pathological substrate for a secondary multiple sclerosis, which is the currently accepted diagnosis.

The medical examiners were unable to establish a direct causal link with GARDASIL ®, stating “that there are no scientific grounds to incriminate GARDASIL ® as the only causal factor for the demyelinating inflammatory pathologies of the central nervous system.

They did however feel that “the vaccine-induced demyelinating inflammatory cascade from which the plaintiff suffers presents all the objective characteristics of medical and legal imputability.

They concluded, after completing a conscientious examination of all the items in the file and substantiating their observations with information from scientific literature, that there is a definite causal link between the first injection of the vaccine and the onset of an acute inflammatory reaction in the central nervous system which then later, after the second injection, led to decompensation of a latent immune process.

They felt that total imputability of the observed damage to the vaccination could be assessed at 50%.

It was not up to the Tribunal to make a general pronouncement on whether the vaccine was defective since a discussion of the public health benefits and risks of the vaccine in question was not on the agenda but it was however expected to determine whether, given the defective nature of the doses administered, the facts before it represented serious, specific and corroborating evidence regarding both Mlle Bourguignon’s personal situation and the specific circumstances (French Court of Appeal, 1st civil, 10 July 2013.  Appeal # 12-21314).

In the case in point, the medical examiners had observed that Mlle Bourguignon presented with a family history of genetic vulnerability making her susceptible to the potential onset of a dysfunctional immune demyelination of the central nervous system.

Her sensory and motor disorders were triggered two weeks after the first injection and then regressed.  Later, two months after the second injection, a cerebral-vestibular syndrome and a sensory-motor condition appeared.

According to the medical examiners, given the substrate of the central nervous system, the vaccination as an immunity stimulator played a role in the onset of the dysfunctional immune and inflammatory cascade.  Stimulation of the immune system by the antigens in vaccines can indeed trigger an autoimmune pathology when there is a genetic predisposition against a particular hormonal and environmental background.

What stands out from the two reports therefore is that there is specific and corroborating serious evidence based not only on chronological sequence but also on factors specific to Mlle Bourguignon.  This is sufficient to establish the link between the two injections of Gardasil which Mlle. Bourguignon received and the onset of her multiple sclerosis.

The patient was not informed of the possibility of such a risk and was therefore not granted the safety she could lawfully have expected.  The vaccine package insert does not mention the risk of central nervous system inflammation while this risk has been scientifically established by medical experts and was known at the time of vaccine authorization.  This is an unusual risk inherent in the vaccination act itself, which does not always result in multiple sclerosis but in the case in point, the risk was real, and due to a predisposition, multiple sclerosis was triggered.

The manufacturer is therefore deemed responsible as per articles 1386-1 and 1386-4 of the French Civil Code.

Sanofi Pasteur MSD’s insurance company must therefore make an offer of compensation for the injury caused.

4.  The Injury: 

Mlle. Bourguignon has not recovered her health.

The injury, with the exception of her two-year absence from school, was totally and properly assessed as is by the medical examiners.  The examiners formally excluded any temporary aesthetic injury.

According to the examiners, 50% of the injury sustained was due to a pre-existing condition.

 

Judgment:

Article 1: Sanofi-Pasteur MSD’s insurance company, Marsh S.A. must make Mlle. Bourguignon an offer of compensation amounting to 50% of her claims as specified below:

– Temporary Total Functional Disability: 73 days from 13th March to 2nd September 2011, dates as specified by the medical examiners.

– Temporary Partial Functional Disability:

    • Category IV: 41 days from the 22nd March to the 1st April 2011, then later from the 9th April 2011 to the 8th May 2011.
    • Category III: 10 days from the 27th May to the 5th June 2011
    • Category II: 62 days from the 1st March to the 18th August 2011, then later from the 3rd September 2011 to the 30th October 2012 which was the day of the medical examination.

– Assistance of an Unskilled Third Party Assistant (her mother):

    • 3 hours per day during the periods of category IV temporary functional disability,
    • 2 hours per day during the periods of category III temporary functional disability,
    • 1 hour per day during the periods of category II temporary functional disability.

– Permanent Functional Disability at the minimum rate of 5%

– Absence from School: loss of two academic years

– Suffering experienced: assessed at the minimum rate of 4/7

Article 2:  If Mlle. Marie-Océane Bourguignon does not receive an offer within four months from receipt of this notice, it will be her responsibility to request ONIAM (Office National d’Indemnisation des Accidents Médicaux, the French National Medical Injury Compensation Authority) to come up with an alternative offer.

Article 3:  This notice will be sent to all interested parties, to ONIAM and to the lawyers and insurance companies concerned, by registered letter with acknowledgement of receipt.

A copy will be sent to Mlle. Marie-Océane Bourguignon’s medical team within her local Social Security unit.

Presiding Judge

Patrick Mairé

 

(A special thanks from the SaneVax Team to Helen Kimball-Brooke for providing the translation of this document.)

Article complements of SaneVax.org

 Marie –Océane, thank you to you and your parents in leading the way for so many other families affected by Gardasil/Silgard/Cervarix injuries.  It is great news that French authorities have granted an award for the difficulties, and congratulations for taking the next step with a criminal court.  How considerate and gracious of your family to think of others at such a challenging time, and make efforts to get the word out to other families so they do not incur these same difficulties.

Your actions speak highly of you, and I have included a video clip as a little gift.  I find that uplifting entertainment is good for the soul.  I hope you and your family enjoy the following clip. 

Your friend, jen  🙂

 

 

Autism: More Laughable Science#vaccines#autism#ASD

by: ,                                            

Don’t these stories just make you laugh? CDC, WHO, and pharmaceutical industry sponsored research such as: old moms and old dad’s cause autism, living next to a freeway causes autism, autism begins in the womb, or this new research that shows autism may be connected to a woman’s use of antidepressants during pregnancy?

Two things are clear: one is that toxins play a role in the autism epidemic and the other is that autism is a man-made epidemic.

To the point that toxins play a role:

Maybe older parents today have accumulated more toxins because the corporate world and our governments are dumping more and more of them on us than happened to parents 100 years ago.

Maybe it is because living next to a freeway, or a coal plant, or other big industry that spews toxic pollutants increase a person’s toxic exposure and load.

Maybe it is because women are now pushed to receive flu vaccines (oftentimes mercury laden ones) and other vaccines
while they are pregnant…

Read the Entire Article Here

The Vaccine Bubble#Vaccines#Autism#Health

by Michael Belkin                     

 My business involves advising portfolio managers about asset allocation in global financial markets. During my career, I have observed several extreme speculative bubbles, including the Japanese stock market in the late 1980s, the NASDAQ frenzy in 1998–2000 and the U.S. housing bubble from 2006–2008.

These bubbles all ended in tears. I see the same elements now in the pharmaceutical industry’s preoccupation with vaccines. I coined the term “vaccine bubble” (in the book Vaccine Epidemic) to describe the economic and psychological factors that are driving the obsession with and over-investment in vaccines. The psychology of making big profits is causing a lemming-like rush into vaccine research and production. Ultimately, many of these companies and vaccine products will likely turn out to be flash-in-the-pan nobodies and nothings that simply waste investment and get discarded on the ash heap of medical history. In the meantime, families and individuals need to educate themselves and make informed decisions about vaccine acceptance or refusal.

The business model of vaccine manufacturers relies on compulsion—you must take their product, or else.

Investing in Health
Taking pharmaceutical company advice about vaccine safety and efficacy is like trusting a stockbroker or real estate agent to tell you the market is in a bubble. As investors and homeowners have learned the hard way, those with corrupt financial or professional incentives cannot be relied upon to provide trustworthy advice.

From a financial and industry perspective, here is what you need to know. Vaccines are licensed by the FDA and recommended by the CDC’s Advisory Committee on Immunization Practices (ACIP). Vaccine manufacturers perform (or outsource) their own efficacy and safety studies, so there is plenty of wiggle room for juggling the data. Manufacturers can choose their own placebo to either flatter efficacy or safety. If you think vaccine safety studies use saline solution for a placebo, think again.

The Merck Manual (the pharmaceutical company’s best-selling series of medical textbooks) defines an adverse reaction to a vaccine: “Encephalitis is inflammation of the brain that occurs when a virus directly infects the brain or when a virus or something else triggers inflammation…. Encephalitis can occur in the following ways: A virus directly infects the brain. A virus that caused an infection in the past becomes reactivated and directly damages the brain. A virus or vaccine triggers a reaction that makes the immune system attack brain tissue (an autoimmune reaction).”

Thus, an adverse vaccine reaction that causes brain damage (encephalitis) has the same result as a complication from an infectious disease like measles. In vaccine safety studies, manufacturers can disguise the neurological damage caused by the vaccine they are testing by using another vaccine (or another substance that contains an aluminum adjuvant) known to cause neurological adverse reactions as placebo. The standard language they use is: “Adverse reactions were no different than placebo.” They don’t mention that the placebo causes neurological adverse reactions…

 Read the full article here

 therefusers.com

Aluminum in baby formula and vaccines#Family#ASD#Vaccines

Aluminum in baby formula and vaccines                              

by Sima Ash, CHom, CNC

(NaturalHealth365) Over the last few years, newborn babies have been overexposed to aluminum with potential harmful consequences. Babies and particularly newborn babies, are at increased risk of aluminum toxicity because of their immaturity.

According to the World Journal of Pediatrics, researchers looked at the role of aluminum in parenteral nutrition solutions, in adjuvants of vaccines and in pharmaceutical products. The researchers conclude that pediatricians and neonatologists must be more concerned about aluminum content in all products our newborns are exposed to, starting from monitoring aluminum concentrations in milk and soy-based formulas in which they state, there is still too much aluminum….

Continue reading the article here

Toni Braxton, Autism, and Vaccines: Maybe it’s just a coincidence#vaccines#ASD#health

Toni Braxton, Autism, and Vaccines: Maybe it’s just a coincidence      

  by:

 In a Fox News article, singer Toni Braxton says: “Maybe it’s just a coincidence that after my son’s first MMR vaccine, I began to notice changes in him.” The article then states she noted “that after that he wasn’t responsive to affection or as high-spirited as he was before the vaccine.”

The Greater Good says, what a strange coincidence, the same story has been reported by thousands of parents the world over! How could this be?

Nevermind the literally dozens of scientific papers published in peer-reviewed journals documenting and exploring a link between autism and “routine” childhood vaccines. The blog Adventures in Autism has a running list of this research with the tally now 86 papers connecting vaccines and autism, but health and medical officials have ostensibly not yet learned to read as they claim no such research exists.  Go figure.

Interestingly Ms. Braxton also says she has the autoimmune disease lupus. Readers might have noticed there seems to be an epidemic of autoimmune disease in the world today. Wonder what is messing up all these folks’ immune systems to cause this?

Maybe it has something to do with all the vaccines being given today as research has found that a few vaccines in mice can overwhelm the immune system causing autoimmune disease and immune system dysregulation. Surely this could never happen in humans…

Continue reading the article here

www.greatergoodmovie.org

Family Health Care Choices#vaccines#health#ASD

FAMILY HEALTH CARE CHOICES 
Interesting Image
 Everyone wants to choose what is best for their family when it comes to health care. So…..how do you choose what’s best for your family, given the variety of health care alternatives today? Basically, it comes down to two main categories of health care: the traditional medical model (allopathic) and the alternative natural health care model. They differ greatly in their approach to illness/disease.
 
MEDICAL HEALTH CARE MODEL
 
In the medical health care model, disease is the result of genetics and germs. It “happens” is to us; we have no real control over it. The body is made up of parts and each part is cared for by a unique provider who is only interested in that part, rather than the body as a whole entity.
 
Symptoms and testing determine diagnosis, which is typically treated with medications, surgeries or other treatment therapies/modalities (ie; radiation therapy). What works for one person must work for all, and doctor knows best-so patients are expected to follow all instructions.
 
 
NATURAL HEALTH CARE MODEL
 
The natural health care model, on the other hand, views the individual as largely responsible for his/her own illnesses based upon lifestyle choices, reactions to stress, exposure to environmental factors, etc. This model views the human body as a whole; any threat to one body part is a threat to all body parts.
 
The body has the ability to heal itself, without drugs or surgery interventions, with the help of natural therapies that work differently for different individuals. Individuals play an important role in maintaining their health which is more than just the absence of disease.
 
True health is optimal well-being in all aspects of oneself-physical, mental, emotional and spiritual.
 
WHICH MODEL IS RIGHT?
 
It is your duty to be informed about the aspects of both health care models so that you can make intelligent decisions about your family’s health care. You may subscribe to one mode and use the other when necessary.

French Vaccine Debates: What immediate measures are required?#vaccines#health#ASD

SaneVax-FeaturedBy Attorney Philippe Vanlangendonck, guest author from Belgium

Translated by Helen Brooke Kimball, European Forum for Vaccine Vigilance (EFVV)

The Colloquium and public hearing on the aluminium in vaccines, held in Paris on the 22nd May 2014: What immediate measures are required?  Mandatory genetic tests before any aluminium-containing vaccine, or immediate moratorium on these aluminium-containing vaccines?

As an attorney registered with the Brussels Bar and defending vaccine victims, I was honored to be able to attend these two important scientific meetings held on the 22nd of May 2014 at the French National Assembly in Paris.  It is at present too early to grasp the full extent and impact of these discussions, the scope of which was vast.

Vaccine Safety Debates

Vaccine Safety Debates

In the morning, E3M (Macrophagic myofasciitis sufferer support group) had invited internationally renowned medical consultants to take part in a colloquium called “Aluminium and Vaccines: International expertise requires action;” and in the afternoon, OPECST, the Office parlementaire des choix scientifiques et technologies, the equivalent of the British House of Commons Science and Technology Committee, had organized a public hearing, open to the press and called “Vaccine Adjuvants: A Controversial Question”.

When one attends a scientific meeting in a political setting such as this and the presence of a minister is announced, the said minister often sends a replacement at the last minute, due to his busy schedule, but on the 22nd of May, it was the exact opposite which happened and this is remarkable enough to be highlighted.  In fact, a correction had been included in the introductory section of the OPECST public hearing programme, informing those attending that Mme. Marisol Touraine, French Social Affairs and Health Minister would be present.

So the French Health Minister attended this public hearing, the profile of which was raised by her presence. The consequences of this for her, as political figure responsible for the proceedings, are clear because by attending this public hearing she cannot later claim not to be aware of what took place.

In fact, any decision in the field of health must take the latest scientific advances and knowledge into consideration.

On the 22nd of May 2014, the latest scientific and technical knowledge in the field of health were presented:

  1. Professor Yehuda Shoenfeld, director of the Zabludowicz Centre for autoimmune diseases and international specialist on immunity, pointed out that certain individuals have a genetic predisposition to much greater and more serious reaction to immune system stimulation in the form of aluminium salt-containing vaccines.

 

  • Professor Yehuda Shoenfeld also informed those attending that we already have genetic ‘tests’ which can determine, before any vaccine is administered, whether an individual’s genetic makeup is such that he may be susceptible in the long term to a potentially very serious auto-immune reaction.

 

Now that the matter has been so clearly outlined in a political setting, the only valid criterion to take into account is that of current scientific knowledge and progress.

As of today, current scientific knowledge and progress has revealed that aluminium is responsible (as an isolated triggering factor or combined with other factors, including the presence of an antigen) for what can be called vaccine-induced illness, or, depending on the case, illnesses which did not naturally exist pre-vaccination and which the individual therefore contracted through aluminium toxicity; as such, he or she would NEVER in his/her life have contracted this disease since without the presence of aluminium, his/her genetic predisposition to serious reactions when exposed to aluminium COULD NOT have caused this illness, e.g. macrophagic myofasciitis.

In other words, no individual even genetically predisposed would ever contract such an illness unless he or she were exposed to the aluminium in a vaccine.

What all this means is that either a genetic ‘test’ would need to be performed before any vaccination (particularly if the vaccine contains aluminium) or no vaccine containing aluminium could ever be mandated.

Professors Exley and Gherardi had also made the same observations regarding the toxicity of aluminium.

On another matter, the fact that Mme. Marisol Touraine, French Health Minister, had taken a public stance during the French presidential campaign in favour of freedom of choice for families faced with aluminium salt-containing vaccines for their children, shows that she is fully aware of the problem and the urgent need to take concrete measures as soon as possible.

Against this background, lack of immediate action, no action or delaying the adoption of the essential measures required would inevitably result in a scandal similar to that of contaminated blood.

The problem is also that the presence of unknown disease makes it very difficult to recognize the disease and treat people suffering from vaccine-induced ailments.

As far as Belgium is concerned, I am working on a letter which I will send to the head of ONE (Office de la Naissance et de l’Enfance), the Belgian Birth and Childhood Authority.

Article compliments of SaneVax.org

The Search for Safer Vaccines#ASD#Autism#Vaccines

 by

 

Vaccine-injured children who end up with autism are quietly winning their cases in federal court, but only when they focus on using the more general terminology of “brain damage” rather than calling it “autism.” 

Take the tragic case of little Elias Tembenis. It could teach us something about how to make vaccination even safer for at risk children. Who could be against the idea of making vaccination–or anything–as safe as it can possibly be? 

Yet raising this simple and logical question has largely been made taboo by pharmaceutical interests and vaccine activists who have long fought a PR campaign to squelch any discussion about vaccine safety and the autism connection; and have falsely portrayed journalists and researchers who pursue it as “anti-vaccine.” The vaccine pharmaceutical activists troll the web for scientific studies and articles that investigate vaccine side effects and then use social media, bloggers and other forums to launch their attacks and incorrectly claim the autism link has been “debunked.” They monitor and edit Wikipedia pages in an effort to downplay research that demonstrates associations between vaccines and autism, and to disparage those who investigate the links. They apply pressure to managers of news organizations that employ journalists who dare to explore the factual connections between vaccines and various serious side effects. 

Sadly, since the Tembenis case, the government has not — at least publicly — done much to answer the questions that it and many others pose: why are the vast majority of kids apparently vaccinated safely, but a minority become seriously ill, brain-damaged or even die…

 

Read the entire article here

       sharylattkisson.com