Database Tracking Without Your Consent

Database Tracking Without Your Consent

Database Tracking Without Your Consent Should Worry Moms

Currently, the Rhode Island Department of Health (RIDOH) has a database, called Kidsnet, and your child’s information is there forever without your consent. This database has all RI resident minor children enrolled in it, and it’s likely you’ve never heard of it. Why is that?

First, it is a robust database tracking things well beyond what you may want tracked, and leave you wondering why such a database needs to be held within the RIDOH.

For instance, it records who lives in the home with the child, and it also tracks blood specimen from birth. Since when is a signature or voluntary consent not needed for DNA data storage? It tracks if you’ve ever enrolled in programs like WIC or Early Intervention.

Mothers may be especially unimpressed to find out that they are tracking if the child was born vaginally, or by c-section. A mother’s level of education, and whether or not the mother was married at time of time of birth are fields in this database.

Is this the kind of data tracking that we want to happen without our consent or approval?

The icing on the cake to this Kidsnet is you cannot delete the file. RIDOH will not remove it regardless of your request. You may only block your child’s file— so that only the RIDOH can see it, and not other signed in accounts.

RIDOH will continue to track and look at your file, while your objections fall on deaf ears. Want to block your file? Well, they go out of their way to make that inconvenient. You need to call the RIDOH then have your doctor witness you signing a form in their office.

We are in the 21st century, using complex databases tracking data without consent, and yet you can not use a online portal or notarized letter to request that our children’s information is blocked. According to the RIDOH, we must call then wait to sign at doctors office to block our child’s data. An electronic file that we should be able to have completely removed and deleted from the system.

Legislation H5541 has been introduced this year, and has a hearing date scheduled for Mar 13th at Rhode Island State House. This legislation expands the Kidsnet database to all adults in RI as part of the National Adult Immunization Plan.

It renames the database Rhode Island Child and Adult Immunization Registry (RICAIR). This database will be set to automatically enroll all adults residing in the Ocean State. This expansion of data mining without consent will now be for every Rhode Island resident no matter the age. When RI has an inflated budget that over spends beyond our revenue, why are we even considering putting more tax dollars to bureaucratic control for something we don’t have an actual need for especially considering the recent UHIP disaster.

National Adult Immunization Plan is an actual plan from HHS, and Goal 3 is increase community demand for adult vaccinations. Goal 4  Foster innovation in adult vaccine development and vaccination-related technologies. This database bill falls into that plan. Do you feel you need multiple more vaccines as an adult? Just a few months ago the FDA approved the HPV vaccine to be expanded to age 45, do you want to be bugged about getting a HPV vaccine? There seems to be a pattern with RI Dept of Health, moving forward with choices that are dollar driven and not driven by a need or want of the RI residents. Rhode Island does not have epidemics for anything a vaccine is available for.

If you don’t want to be automatically enrolled in a government database that you can not delete your file from then please oppose bill H5541. Please attend the hearing at 4:00pm on Wednesday the 13th at the Rhode Island State House. Citizens are encouraged to testify in person in room 101 or submit written testimony to the committee. Secretary of the H.E.W. committee can be contacted via lcataldi@rilegislature.gov

.

Aimee Gardiner

Aimee@NOHPVmandateRI.com

Instagram & Twitter @MyRightsRI

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http://www.health.ri.gov/publications/metadata/KIDSNETDataDictionary.pdf

https://www.hhs.gov/sites/default/files/nvpo/national-adult-immunization-plan/naip-path-to-implementation.pdf

https://nohpvmandateri.files.wordpress.com/2019/02/h5541.pdf

http://www.health.ri.gov/programs/kidsnet/about/confidentiality/#whatparentscando


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New England continues push to mandate Gardasil despite numerous Deaths reported to VAERS

New England continues push to mandate Gardasil despite numerous Deaths reported to VAERS

Below is an article that was originally found on Medium but was censored regardless of it having a list of reference links. The author has sent the article to us to publish to be sure it still reaches as many eyes as possible. Sign up for our blog to be notified each time there is a new post.

The writer is Jennifer and you can find her on Minds.com/JCherry17

CT Pushes for HPV Vaccine Mandates Despite Numerous Deaths Reported to VAERS

(MA also has a bill to mandate and RI currently has already mandated it for 7th graders)

Informed consent is a human right. Having a full understanding of the benefits, and the risks of a medical procedure are paramount to making a conscious healthcare decision. Children are not able to give informed consent, they are not mature enough. When it comes to medical procedures, you cannot keep parents in the dark.

Currently the Connecticut General Assembly is considering SB 858, which would permit prophylactic treatment of minors for sexually transmitted diseases without the consent or knowledge of a parent or guardian. Prophylactic means preventative. The preventative treatment is the HPV vaccine given to children 9 years and up. Both boys and girls without informed consent. There is also a bill from public health 7199, to mandate HPV vaccine to all children entering 9th grade.

According to the Connecticut State Budget, “funding of $9,617,802 in FY 18 and $9,517,802 in FY 19 to make the HPV vaccine universally available to privately insured children. Included in the FY 18 funding total is $100,000 to support a related educational campaign.” That’s over nineteen million dollars allocated toward a very controversial vaccine. This for children who have health insurance, which already pays for their vaccinations. There are two kinds of HPV vaccines on the market today, Gardasil by Merck, and Cervarix by GlaxoSmithKline. In Connecticut Gardasil is the common vaccine for HPV.

The Gardasil vaccine was fast tracked by the FDA and approved in June of 2006, after a six month priority review process. Most vaccines take at least 10 months to review. HPV was fast tracked because the manufacturers claimed their vaccine prevented cancer. Drugs for cancer treatment and prevention can be fast tracked. However, there is no clinical data to support this.

Vaccines are a medical procedure that come with clear risk. When children are given the HPV vaccine they are told to wait for 15 minutes incase of syncope. According to American Family Physicians, a peer review journal, “Syncope is an abrupt and transient loss of consciousness caused by cerebral hypoperfusion. Syncope is classified as neurally mediated, cardiac, and orthostatic hypotension.” However, HPV is the most common sexually transmitted disease and typically clears up on its own in those infected without incident. Not all infections with HPV lead to cancer. Death from cervical cancer in the United States is very low thanks to early detection from pap smears. Ironically, according to Biologics Blood Vaccines, “Gardasil has not been evaluated for the potential to cause carcinogenicity or genotoxicity.”

The Gardasil vaccine is made with HPV virus, yeast cells, amino acids and amorphous aluminum hydroxyphosphate sulfate, AAHS. AAHS, is a proprietary adjuvant not approved by the FDA, “When evaluating a vaccine for safety and efficacy, the FDA considers adjuvants as a component of the vaccine; they are not licensed separately.” However, the FDA did license Glaxo Smith Cline Cervarix adjuvant, AsO4, “In the United States, the only adjuvants currently licensed by the FDA to be part of vaccines are aluminum salts and arsenate (AsO4), an adjuvant that contains aluminum hydroxide and monophosphoryl lipid.”

The question that remains is why did the FDA separately license one adjuvant versus the other? Ironically, Merck does not have to share anything about their AAHS adjuvant because they own the patent. They also enjoy indemnity from tort law via the Vaccine Injury Act of 1986, which grants vaccine manufacturers immunity from lawsuits due to injury or death from their vaccine products in the United States. It is alarming that any state would mandate vaccines while consumers are left in the dark and forced to take a risk.

Many experts question both the safety and efficacy of the HPV vaccine. Leading aluminum researcher, Professor Chris Exley, who has studied aluminum for over 30 years writes,“Unfortunately Merck, the manufacturer of this adjuvant, has not made it available for any independent analyses, never mind safety testing.” Adjuvants work by stimulating the immune system to react. Aluminum is a neurotoxin that is used to aggravate a response in the body. When aluminum is injected into the bloodstream it builds up over time and can travel to the brain. Exley continues, “It is undeniable that a small proportion of individuals receiving vaccines which include aluminum adjuvants experience what have been called severe adverse events and such ‘events’ include brain encephalopathies. These severe adverse events are almost certainly caused by aluminum adjuvants.”

Children’s Health Defense, founded by Robert F. Kennedy Jr., states this about the AAHS adjuvant, “Researchers are particularly concerned with Merck’s highly immunogenic adjuvant, Amorphous Aluminum Hydroxyphosphate Sulphate (AAHS). Gardasil and Recombivax are the only vaccines licensed to contain AAHS. Some scientists believe it may contribute to serious autoimmune conditions referred to as Autoimmune/Inflammatory Syndrome Induced by Adjuvants or ASIA.”

Specialist in HPV and a developer of Gardasil, Dr. Diane Harper, appeared on CBS in 2008 and had this to say,“It is unacceptable to mandate any vaccine without first testing it for effectiveness, safety, and long-term side effects. The Gardasil vaccine may be an important step in preventing cervical cancer, but it is a step that may cause other harm.” This was eleven years ago, and since then thousands of children across the United States and abroad have reported adverse reactions to Gardasil.

In June of 2014 a claim was filed by Attorney Don Manuel Sáez Ochoa of Spain’s high court, Health Impact News reports, “The complaint states that Merck Laboratories failed to use an inert placebo during clinical trials, thereby manipulating data and marketing Gardasil under false pretences. On July 30, the Judge decided to open criminal proceedings and investigation of the facts. The first criminal case in Spain regarding Gardasil injuries and potential criminal liability.” France is also pursing litigation. Prevent Disease writes,“The parents of the five families contend that vaccines caused their children’s disabilities have joined forces to take Glaxo Smith Kline, Pfizer and Sanofi to court in hopes that the courts will acknowledge the side effects of vaccines and award compensation to their disabled children.”

Japan took the HPV vaccine off the recommended schedule just two month after it had added it due to adverse reactions across the country. To paraphrase investigative journalist Jeffery Jaxen, ‘Sin Hang Lee (former Associate Professor at Yale University and current Director of the Milford Molecular Diagnostics Laboratory) appeared before the Japanese government’s Advisory Council. Dr. Lee reported that HPV DNA fragments bound to the AAHS adjuvant were found in 16 unopened vials of Gardasil, sent to Milford Medical Laboratory from nine countries. Fragments were also found in postmortem blood and spleen samples from the autopsy of an 18-year-old New Zealand girl who died after Gardasil vaccination.’ The adjuvant combined with the DNA fragments can cause illness and death.

Dr. Bernard Dalbergue, former pharmaceutical industry physician for Merck, was quoted in 2014 while doing an interview for a French health magazine, “I predict that Gardasil will become the greatest medical scandal of all time,” The Gardasil vaccine is the most expensive vaccine on the market. Merck, makers of the failed drug Vioxx, that injured thousands of people and was taken off the market due to high risk of heart attack and death, have paid out billions of dollars in lawsuits. Tort law for pharmaceutical drugs is applicable, but not for vaccines. Merck was seriously injured financially, and is still in litigation over Vioxx. Vioxx like Gardasil, was fast tracked by the FDA in 1999 and pulled from the market in 2002.

Yet the FDA says the DNA fragments that Dr. Lee was concerned about are not a problem. The fragments are part of the vaccine, “According to the FDA on HPV and DNA fragments, “Because the vaccine does not contain a viral DNA strand from HPV, it should not cause HPV or cancer. Instead, it ought to tigger an antibody reaction to guard the host from being infected by the virus.” Yet, Italian advocacy group, Corvelva found many contaminations in the HPV vaccine. One shocking discovery, “Human and Mouse DNA: their origin is not known. It may be that human DNA could instead be a cross-contamination from other cell lines used for the production of vaccine. These DNA could interact with the adjuvant aluminum and cause inflammatory and autoimmune reactions.”

With all of this evidence and science, it appears that the CDC and the FDA, have been corrupted. The heads of the CDC and FDA are appointed, not elected. The doors revolve from industry to government and vice versa. Two examples illustrate this well. Dr. Julie Gerberding was the, director of the Center for Disease Control and Prevention from July 2002 thru January 2009. Meanwhile, in February of 2008, Gerberding had been named president of Merck’s vaccine division. The CDC also holds patents in vaccines and benefits financially from them. Attorney Robert F. Kennedy Jr clarified this relationship, “ (the) CDC is a subsidiary of the pharmaceutical industry. The agency owns more than 20 vaccine patents and purchases and sells $4.1 billion in vaccines annually” In a second example, Michael R. Taylor had a long career in government and also served as vice president for public policy for Monsanto. In 2009, Taylor was the FDA commissioner. Later he served in a newly created position as Deputy Commissioner for Foods util 2016.

Even more egregious is William Thompson, a CDC researcher blew the whistle in 2014 on a coverup linking MMR to autism. Eco Watch writes, “Thomas Frieden, the director of the Center for Disease Control (CDC), has blocked CDC whistleblower, Dr. William Thompson, from testifying on scientific fraud and destruction of evidence by senior CDC officials in critical vaccine safety studies regarding the causative relationship between childhood vaccines and autism.” Invariably, this is the study they use to say vaccines do not cause autism.

In 2019 Dr. Zimmerman, the lead witness for the government in vaccine court in 2007, said he was taken out of context when he said vaccines do not cause autism. He meant vaccines did not cause autism in the particular case he was called as a witness for. Investigative journalist. Sheryl Atkinson covered the story on Full Measure and has made his affidavit available for the public. Dr. Zimmerman, “More specifically, I explained that in a subset of children with an underlying mitochondrial dysfunction, vaccine induced fever and immune stimulation that exceeded metabolic energy reserves could, and in at least one of my patients, did cause regressive encephalopathy with features of autism spectrum disorder.”

VAERS The Vaccine Adverse Events Reporting System was put in place to monitor problems with vaccinations after the 1986 Vaccine Injury Act. The system only captures between 1 and 10 % of all vaccine injuries. Doctors, nurses, caretakers, and parents can file reports with VAERS. As of December 2018, According to SaneVax.org 60,714 injuries from HPV vaccines have been reported to VAERS, 458 deaths,15,401 ER visits, and 6,047 extended hospital stays. VAERS is a public data base that anyone can search.

There is much that can go wrong with the HPV vaccine. Without informed consent giving any vaccination is a violation of human rights. Why has the state of Connecticut purchased the HPV vaccine for so many years? There are now two bills for HPV vaccine mandates before the state legislator, SB 858, and PH 7199. Another vaccine bill, SB 94, intends to reduce the age from 18 to 12 to allow pharmacists to administer vaccines. The total budget to purchase vaccines in Connecticut is ninety one million dollars. Yet we can’t pay back the money the state borrowed from teacher’s pensions.

When it comes to vaccines, who is writing the laws? According to a study in American Journal of Public Health on HPV and state vaccination policies, “Respondents in every state commented on how effectively Merck prepared the political environment for the introduction of school-entry mandates and other legislation. The company carried out this objective through marketing campaigns to consumers and physicians and direct outreach to political interest groups.”

Not all vaccines work for all people, medical care is not a one size fits all. Some people can be severely injured by them. Where there is risk there must always be choice. “The voluntary consent of the human subject is absolutely essential.” The ten points of The Nuremberg Code.

 

All three states have Health Choice non profit groups. All three states are also fighting against mandates of HPV vaccines for attending school. ~~  NOHPVmandateRI.com  ~~   NoHPVmandateMA.com  ~~   HealthChoiceCT.org      —    you can connect with activists to get involved.

 

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1.State of Connecticut, https://portal.ct.gov/-/media/Departments-and-Agencies/DPH/dph/infectious_diseases/immunization/cvp/update-HPV-9-expansion-11-2-17-pdf.pdf?la=en

2. State of Connecticut Budget, https://www.cga.ct.gov/ofa/Documents/year/BB/2018BB-20180214_FY%2018%20and%20FY%2019%20Connecticut%20Budget.pdf

3. American Family Physicians,https://www.aafp.org/afp/2017/0301/p303.html

4.GARDASIL https://www.fda.gov/downloads/biologicsbloodvaccines/vaccines/approvedproducts/ucm111263.pdf

5.FDA / AAHS, https://www.fda.gov/BiologicsBloodVaccines/SafetyAvailability/VaccineSafety/ucm187810.htm

6. Chris Exley,https://www.hippocraticpost.com/infection-disease/aluminium-adjuvants-vaccines/

7. Children’s Health Defense, https://childrenshealthdefense.org/news/mercks-recombivax-vaccine-shortage-causes-reduced-deaths-in-babies-a-natural-experiment

8. US Census, http://www.allcountries.org/uscensus/129_death_and_death_rates_by_age.html

9.CDC,https://www.cdc.gov/nchs/data/databriefs/db37.pdf

10.FDA ApprovedProducts/UCM111263.pdf(https://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/

11.CDC Pink Book, https://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/B/excipient-table-2.pdf

13.Dr. Harper, https://www.cbsnews.com/news/serious-questions-about-hpv-vaccine-07-07-2008/

14.Spain Sues For Brain Damage From HPV,http://healthimpactnews.com/2014/lawsuits-for-hpv-vaccine-damages-begin-in-spain/

15.American Journal Public Health, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483914/

16.Corvelva,https://www.corvelva.it/it/

17.EcoWatch, https://www.ecowatch.com/cdc-vaccines-autism-2051536402.html

18.Sheryl Attkisson, https://sharylattkisson.com/2019/01/06/dr-andrew-zimmermans-full-affidavit-on-alleged-link-between-vaccines-and-autism-that-u-s-govt-covered-up/

19.Jeffery Jaxen, https://www.jeffereyjaxen.com/blog/one-big-reason-to-consider-not-getting-the-hpv-vaccine

20.Dr Bernard Dalbergue,http://ddata.over-blog.com/xxxyyy/3/27/09/71/2012-2013/Juin-2013/Dr-Dalbergue–Gardasil–plus-grand-scandale-de-tous-les-tem.pdf

21.Spain Lawsuits, https://www.naturalblaze.com/2014/07/spain-first-case-filed-against-hpv.html

22.http://preventdisease.com/news/14/021214_Families-Battle-Big-Pharma-Side-Effects-Vaccines-Disabled-Children.shtml

22.Nuremberg Code, https://history.nih.gov/research/downloads/nuremberg.pdf

Merck’s Gardasil science (lack thereof) taken to court

The article you are about to read is long. We hope you take the time to read it. Merck was brought before our justice system, and not just the mock of a court system called “vaccine court” when you have a vaccine injury. Our fight has been against the mandate of the HPV vaccine and to advocate informed consent. When reading the studies from Merck there has always been reason to not trust that the advertised benefit was worth the risk of injury; Now via these top lawyers in the case described- Merck has to answer for Gardasil.

Please forward this article to your representative and your senator (GardasilCourtCase.NOHPVmandateRI.com). Please call them and tell to support reversing the HPV mandate in RI, and to support H5165 for philosophical exemption. This case shows why informed consent and ability to act based on the information learned is imperative for all citizens.

kids world

=By Lyn Redwood, R.N, M.S.N., President, Children’s Health Defense

On Wednesday January 9th, I attended Science Day Presentations in the Jennifer Robi vs. Merck and Kaiser Permanente case in Los Angeles Superior Court. I want to report to our community on the outcome of this important event and provide some personal commentary.

It is difficult to describe the feelings of elation and frustration that I experienced during the full day of furious arguments that began at 9:30 am before Judge Maren Nelson. Due to the restrictions of the National Childhood Vaccine Injury Act, my son and thousands of children like him, have never been able to have their injuries acknowledged in a court of law.  This day gave families around the globe whose children’s health was permanently harmed by the HPV vaccine a glimmer of hope that their injuries and suffering would finally be acknowledged. The frustration I felt came from the obvious fact that the science relied on by our federal agencies to approve the HPV vaccine was criminally inadequate and that Jennifer’s injuries and those of the thousands of others like her could have been prevented.

Prior to Science Day, plaintiffs’ attorneys worried that because Judge Nelson threw out a $472 million 2017 jury verdict against Johnson & Johnson for causing ovarian cancer in women exposed to its asbestos-containing baby powders, the Court might not be very receptive to their arguments here. However, Judge Nelson gave scrupulous attention to the science presentations by both sides and clearly seemed to be approaching the Robi case with an open mind.

A red-letter day

After 20 years of advocating for vaccine safety, this was the first time that I’ve watched vaccine science issues adjudicated in a true court of law.  It was truly a red-letter day. Jennifer’s lawyers brilliantly laid bare Merck’s anemic case for Gardasil, dissecting the science in withering presentations challenging both the efficacy and safety of the Gardasil vaccine, and then chronicling the horrifying agency and corporate corruption that lead to its approval.

Jennifer Robi is a 24-year-old former athlete and scholar who has been confined to a wheelchair since receiving her third Gardasil vaccines at age sixteen. She suffers continual uncontrolled neuro/muscular contractions (jerking) and postural orthostatic tachycardia syndrome (POTS) and many other symptoms of systemic autoimmune dysregulation.

Jennifer’s attorney, Sol Ajalat, initially brought her case in Vaccine Injury Compensation Program and then, following a judgment in the program, elected to proceed in civil court. Since VICA (the Vaccine Injury Compensation Act) forbids recoveries for product defect or negligence, Ajalat brought Jennifer’s civil case under the theories that Merck committed fraud during its clinical trials and then failed to warn Jennifer (and, by implication, other injured girls) about the high risks and meager benefits of the vaccine.

In order to support Sol Ajalat and his sons Greg, Larry, and Steve, who compose the Los Angeles firm Ajalat & Ajalat, a blue ribbon A-Team of the nation’s leading plaintiffs’ law firms have joined Jennifer’s trial team. These include the firms most feared by Pharma: Weitz & Luxenberg (countless major pieces of litigation over 30 years), Morgan & Morgan (Vioxx, Phenphen, Breast Implants, Tobacco), Baum Hedlund, (Monsanto $289 million verdict 2018 and the $54 million 2000 verdict against Bayer in Haemophiliac/AIDS case) as well as Children’s Health Defense’s own Robert F. Kennedy, Jr. and Kim Mack Rosenberg (a co-author of The HPV on Trial). The plaintiff’s bar has steered clear of vaccine lawsuits since the 2008 Thimerosal fiasco which nearly bankrupted several big firms. Now, Merck, through its reckless overreaching with Gardasil—a public health flimflam currently emerging as the most dangerous vaccine in history—has brought the nation’s leading trial lawyers back to the brawl.

The three Merck attorneys who made presentations were Dino Sangiamo, Sally Bryan, and Christina Gaarder. Jo Lyn Valoff represented Kaiser.

Gardasil’s super-powered aluminum adjuvant

Plaintiffs began the day with a 2.5 hour presentation. Sol Ajalat first introduced Paul Pennock of Weitz & Luxenberg. Pennock ran through a riveting 50-minute slide show demonstrating how Gardasil’s super-powered Amorphous Aluminum Hydroxyphosphate Sulfate (AAHS) adjuvant over-stimulated the immune systems of vaccine recipients tipping them into autoimmune conditions in which their redlining immune defenses begin attacking their bodies’ own organs. This “autoimmune process” causes a cascade of illnesses that, in Jennifer Robi’s case, resulted in damage and deterioration in diverse organ systems throughout her body.

Victims like Jennifer are left exhausted as the body fights off disease on multiple fronts.  Pennock explained that vaccine makers add aluminum adjuvants (to weak antigens and a long list of other potentially toxic ingredients) to elicit an immune response, hoping to extend the short-term immunity otherwise provided by most vaccines. Among vaccinologists, it’s axiomatic that the duration of immunity correlates directly to the toxicity of the adjuvant; the more toxic the adjuvant, the longer the duration of immunity. Most vaccines provide immunity for only 5-10 years. Gardasil’s promoters were promising lifelong protection, and needed a super toxic adjuvant that would provide this unprecedented level of protection. After all, Merck was promising regulators, pediatricians and the public that inoculations given to 9-12-year-old girls would provide immunity against a relatively rare cancer that typically doesn’t kill until age 58!

Pennock explained that Merck has refused to disclose the contents of AAHS or to provide samples to independent and university scientists for testing.  AAHS, astonishingly, has never been safety tested by government regulators or by Merck. Studies on animals conducted by world renowned independent scientists like Dr. Chris Exley, Dr. Yehuda Shoenfeld, Dr. Chris Shaw and others have found that mice and sheep exposed to aluminum adjuvants, at concentrations comparable to those found in vaccines, develop strange behavioral patterns and illnesses resembling autoimmune diseases.

Using a poisonous placebo in the control group allowed Merck to mask the cascade of injuries suffered by girls in the Gardasil group during the clinical trials.

A parade of deceptive canards

Robert F. Kennedy, Jr. next gave the court an explosive 50-minute presentation of 112 disturbing slides describing the parade of deceptive canards that composed Merck’s clinical trials. Kennedy described a series of fraudulent gimmicks employed by Merck to deceive regulators during the clinical trials including the use of a “spiked” extremely toxic AAHS placebo rather than a true inert placebo that is standard for control groups in blue ribbon safety studies for other pharmaceutical products. Using a poisonous placebo in the control group allowed Merck to mask the cascade of injuries suffered by girls in the Gardasil group during the clinical trials.  Half the girls in the Gardasil group and half the girls in the spiked placebo group suffered serious injuries, including several deaths, in the first seven months of the clinical trials, yet Merck was able to claim that reactions in the study group “were similar to the reactions in the placebo group,” and that, therefore, the vaccine was safe. Merck reported most of these serious injuries as “new medical conditions” not adverse events, dismissing any connection to the vaccine by fiat. Information about this parade of grave injuries appears nowhere in the Gardasil package insert.

Merck committed its boldest fraud in its key clinical trial, Protocol 18.  Merck told FDA that Protocol 18 was the single study in which its researchers gave the control group a true inert placebo.  For this reason, FDA declared Protocol 18 “of special interest.”  However, in reality, Merck appears to have taken the precaution of removing half the aluminum from the vaccines administered to this study group. Plus, The Company laced the “placebo” with a witches’ brew of other toxic chemicals. This study, the only “controlled” study that included children in the target cohort of 9-12-year olds, may not have in fact tested the vaccine that Merck went on to inject into millions of young children around the world. Kennedy told the judge that this is not just scientific malpractice, it is outright fraud!

… Merck’s control groups did not reflect the target population for its drug.

Another tactic utilized by Merck was to purge the study group of anyone with the slightest vulnerabilities to the vaccine or its ingredients despite the fact that the vaccine would ultimately be marketed to girls with the very vulnerabilities excluded during the clinical trials.  This precaution allowed the company to mask effects that occur only in vulnerable subgroups.  Mr. Kennedy drew laughter from the large court room audience when he described how Merck had prescreened the study subjects to exclude people with allergies, immunological or nervous disorders, more than 4 lifetime sexual partners, genetic vulnerabilities to cancer or to any other medical condition, or with any hint of general infection, a history of alcohol or drug abuse, or a serious or chronic illnesses, and so forth. Finally, Merck told its researchers to exclude any individual with “any condition which in the opinion of the researchers might interfere with the study objective.” The remaining participants were an elite club of super healthy individuals. “You couldn’t get into the clinical trials unless you were a superhero,” Kennedy told Judge Nelson. “You had to be eligible for the Avengers.” The problem, of course, is that none of the people receiving the vaccine under CDC’s mandate are screened for these vulnerabilities. In other words, Merck’s control groups did not reflect the target population for its drug.

The mayhem caused by Gardasil

Even these flimflams could not conceal the mayhem caused by Gardasil.  Kennedy showed the court data from Merck’s own package insert showing that 2.3 % of the girls receiving the vaccine complained of symptoms of autoimmune disease within 7 months. Since cervical cancer kills only 1.5 Americans in every 100,000, he noted, “Merck’s own data show that the chances of getting an autoimmune disease from this vaccine are 1000 times the risk of dying from cervical cancer.”

Merck’s own data showed that administering the Gardasil vaccine to girls who had previous exposure to HPV actually raised their risk of developing precancerous lesions (or worse) by almost 45%.

Not only did a heartbreaking 50% of the subjects in both the study group and the spiked placebo group experience a serious adverse event within the seven months of the trial, death rates among girls in the study were double background rates. In fact, the rate for girls during the clinical trials (85/100,000) was 37 times the death rate from cervical cancer!  Birth defects among children conceived during the study period were 5x those of the control group and miscarriages were doubled over background rates. Reproductive problems among vaccinated girls were 10x background rates. Finally, Merck’s own data showed that administering the Gardasil vaccine to girls who had previous exposure to HPV actually raised their risk of developing precancerous lesions (or worse) by almost 45%. This revelation is particularly frightening since sexual behavior is only one of many vectors for acquiring HPV. Many children are exposed in the birth canal. Kennedy cited numerous studies showing many very young children are exposed to HPV, including one in which upwards of 34% of girls had exposure to HPV prior to age 10.

Kennedy closed his powerful presentation by chronicling the parade of corrupt conflicts that caused HHS officials to turn a blind eye to the rife fraud that characterized the clinical trials. Merck loaded the two FDA and CDC panels that approved Gardasil, with paid toadies. He showed that the pharmaceutical industry actually pays 45% of FDA’s annual budget and that NIH and its officials own part of the patents to the Gardasil vaccine and collect royalties on every vaccine sold.  NIH collects tens of millions of dollars annually from Gardasil sales.  Finally, 45% of CDC’s budget goes to promoting and purchasing vaccines.  Merck exerts control over the CDC with millions of dollars in contributions to the CDC foundation, which allows funding for pet projects.  This level of support gives Merck the power to also punish the CDC by withholding funding if displeased by the agency.

Jennifer’s illness due to Gardasil

Nicole Maldonado of Baum Hedlund next described the onset of Jennifer’s illness which worsened with each stage of the three vaccine series and how her symptoms were identical to the symptoms seen among hundreds of injured women during the clinical trials around the world, in places as diverse as Japan, Australia, Colombia, and Denmark (where special clinics have been set up to treat Gardasil’s victims), as well as among many girls here in the United States. These symptoms included menstrual irregularities, gastrointestinal dysfunction, musculoskeletal pain, neurological conditions and even death.

One courtroom observer, a concerned mother identifying herself as Rachel Harris said she felt sick to her stomach at the revelations. Jennifer Robi’s mom told me that she felt elated that Mr. Kennedy had mastered the facts so completely and that their family’s story was finally being told.

The rebuttal

The Defendants’ three-hour rebuttal was mainly toothless. Sangiamo doggedly described six studies, that he claimed were relied upon by the plaintiff, that had been retracted. However, only one of those studies was even mentioned on the plaintiff’s lengthy exhibit list (Plaintiff’s attorneys never referred to it in their briefs) and that study was republished elsewhere after the original journal retracted it under pressure from its pharmaceutical advertisers.

Sangiamo argued that the plaintiff had relied on case studies rather than large scale epidemiological studies of the kind largely funded by industry or the NIH which owns the Gardasil patent and profits on every injection sold.  He cited five of those NIH and industry-authored epidemiological studies that found no causal relationship between Gardasil and autoimmune diseases.  All are plagued by fatal defects such as only looking for a very limited number of potential injuries for a short period of time following exposure to the vaccine, despite the fact that autoimmune diseases can take months or years to manifest.  The authors of these studies had financial ties to Merck.

Finally, Merck’s Sally Bryan rose to the podium to explain to Judge Nelson that Merck’s AAHS adjuvant was safe because of the small quantities of this known neurotoxin in each vaccine.  She told the judge that “the dose makes the poison,” and that even water in large enough doses can be toxic. She pointed out that there are only 225 micrograms of aluminum in each vaccine. To illustrate how small this is, she asked Judge Nelson to imagine a dollar bill – which weighs one gram – cut into 1 million tiny pieces. She pointed out that only 225 of these pieces would be in any Gardasil vaccine, far too little to cause any adverse outcome. So in one breath, Merck was telling Judge Nelson that the amount of aluminum in Gardasil was substantial enough to permanently alter a person’s immune system to prevent cancer for the next half century and, at the same time, small enough to cause no harm.

The path forward

At the end of a long day, Judge Nelson ordered both sides to work out a discovery schedule and to reappear in court on February 7 to resolve any differences.

In Merck’s zealous promotion of the Gardasil vaccine, the company and its allies have shamed parents into vaccinating their children, through a series of misleading ad campaigns which play on parental instincts to protect their children from harm, especially from a disease as frightening as cancer. One commercial depicts young girl and boy actors recounting how they developed cancer from HPV and asking their parents if they knew this could have been prevented. “Did you know – Mom and Dad?”  Jennifer Robi has had the courage to tell a real-life story that the public rarely hears – about the risks of the Gardasil vaccine itself.

Watch RFK, Jr. describe his plan to take this issue to the courts


Original article from Children's Health Defense

 

 

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CDC Recommends Two HPV Shots for Younger Adolescents

CDC Recommends Two HPV Shots for Younger Adolescents

CDC now routinely recommends two doses of HPV vaccine for 11 or 12 year olds to prevent HPV cancers. This recommendation makes it easier for parents to protect their children by reducing the number of shots and trips to the doctor. HPV vaccination is an important cancer prevention tool and two doses of HPV vaccine will provide safe, effective and long-lasting protection when given at the recommended ages of 11 and 12 years. Some of the specifics of the recommendation include:

  • The first HPV vaccine dose is routinely recommended at 11-12 years old. The second dose of the vaccine should be administered 6 to 12 months after the first dose.
  • Teens and young adults who start the series at ages 15 through 26 years will continue to need three doses of HPV vaccine to protect against cancer-causing HPV infections.
  • Adolescents aged 9 through 14 years who have already received two doses of HPV vaccine less than 6 months apart, will require a third dose.
  • Three doses are recommended for people with weakened immune systems aged 9-26 years.

 

 

 

Here is the updated RI DOH website

screenshot_2016-12-04-13-22-37-1

 

 

Here is the press release put out by the CDC

Press Release

For Immediate Release

Wednesday October 19, 2016

CDC recommends only two HPV shots for younger adolescents

Fewer shots offer more incentive to prevent HPV cancers

CDC today recommended that 11- to 12-year-olds receive two doses of HPV vaccine at least six months apart rather than the previously recommended three doses to protect against cancers caused by human papillomavirus (HPV) infections. Teens and young adults who start the series later, at ages 15 through 26 years, will continue to need three doses of HPV vaccine to protect against cancer-causing HPV infection.

“Safe, effective, and long-lasting protection against HPV cancers with two visits instead of three means more Americans will be protected from cancer,” said CDC Director Tom Frieden, M.D., M.P.H. “This recommendation will make it simpler for parents to get their children protected in time.”

The Advisory Committee on Immunization Practices (ACIP) voted today to recommend a 2-dose HPV vaccine schedule for young adolescents. ACIP is a panel of experts that advises the CDC on vaccine recommendations in the United States. CDC Director Frieden approved the committee’s recommendations shortly after the vote.  ACIP recommendations approved by the CDC Director become agency guidelines on the date published in the Morbidity and Mortality Weekly Report (MMWR).

CDC and ACIP made this recommendation after a thorough review of studies over several meetings. CDC and ACIP reviewed data from clinical trials showing two doses of HPV vaccine in younger adolescents (aged 9-14 years) produced an immune response similar or higher than the response in young adults (aged 16-26 years) who received three doses.

Generally, preteens receive HPV vaccine at the same time as whooping cough and meningitis vaccines. Two doses of HPV vaccine given at least six months apart at ages 11 and 12 years will provide safe, effective, and long-lasting protection against HPV cancers. Adolescents ages 13-14 are also able to receive HPV vaccination on the new 2-dose schedule.

CDC will provide guidance to parents, healthcare professionals, and insurers on the change in recommendation. On October 7, 2016, the U.S. Food and Drug Administration (FDA) approved adding a 2-dose schedule for 9-valent HPV vaccine (Gardasil® 9) for adolescents ages 9 through 14 years. CDC encourages clinicians to begin implementing the 2-dose schedule in their practice to protect their preteen patients from HPV cancers.

ACIP, CDC, FDA and partners monitor vaccines in use in the U.S. year-round. These updated recommendations are an example of using the latest available evidence to provide the best possible protection against serious diseases.

Parents Would* Support School HPV Vaccine Requirements if Offered Opt-Out

Most Parents Would Support School HPV Vaccine Requirements if
Offered Opt-Out Provisions
By Carrie Printz
Researchers recently found that parents are more likely to support laws that would make the human papillomavirus (HPV) vaccine mandatory for school entry if their state offered
opt-out provisions. However, the researchers added that such provisions may weaken the impact of these mandates. The study, published in Cancer Epidemiology, Biomarkers & Prevention, was led by William Calo, PhD, JD, a postdoctoral research associate in the department of health policy and management at the University of North Carolina at Chapel Hill.

1
He and his colleagues conducted a web-based survey of 1501 parents between November 2014 and January 2015. Respondents had to have at least 1 child aged 11 to 17 years living primarily in their household. The survey asked parents about this statement: “Some states are trying to pass laws that would require all 11- and 12-year olds to get the HPV vaccine before they are allowed to start 6th grade.” Overall, 21% of participants agreed that such laws were a good idea, 54% disagreed, and 25% said they neither agreed nor disagreed.
Dr. Calo says that the latter group may benefit from public education regarding HPV vaccination and, as they learn about the benefits of vaccination, be more likely to support school- entry requirements. The respondents who disagreed that the laws were a good
idea were presented with a follow-up statement: “Is it okay to have these laws only if parents can opt out when they want to?” When this provision was added, approximately 57% of respondents agreed that school-entry requirements were a good idea whereas 21% disagreed.
Among other findings:
• Nearly one-third of respondents believed that the vaccine was being promoted to make money for drug companies.

• Approximately 40% believed that the vaccine was effective in preventing cervical cancer.
Dr. Calo notes that changing some of those perceptions would help to improve HPV vaccination rates along with legislating school-entry requirements. He adds that any opt-
out provisions also have the potential to weaken the overall effectiveness of HPV vaccination if large numbers of families opt out. As a result, such an option also should include an educational component to encourage patients to carefully consider their decision, he says. States should consider school-entry requirements for HPV vaccination after implementing other approaches, such as centralizing vaccination reminders in state health departments, focusing on HPV vaccination during quality improvement visits to providers, and training physicians to use announcements to introduce vaccination, Dr. Calo notes.

#NOHPVmandateRI comments;

Why does any parent feel it is okay to mandate something that has no impact on a school classroom just because there is an opt out?
No it is not. We should not let the government think they can put more regulations and laws upon our bodies and our children’s bodies. This vaccine has nothing to do with public health policy. It is not transmitted in a casual school or work environment.

HPV Vaccines: Betrayal of the Public Trust?

HPV Vaccines: Betrayal of the Public Trust?

In 2013 multiple news articles reported 44% of American parents refusing Gardasil or Cervarix for their children. Between 2008 and 2010, the percentage of parents concerned about the safety of these two vaccines nearly quadrupled. As of 2010, only 32% of eligible girls were vaccinated against HPV. What is wrong with this picture?

Excerpts from national news sources, March 18-22, 2013:

  • USA Today The percentage of parents who say they won’t have their teen daughters vaccinated against the human papillomavirus increases, even though physicians increasingly recommend the vaccinations. Concerns about safety and side effects for the human papillomavirus (HPV) vaccine have increased among parents: 16% cited these fears as the main reason they did not have their daughters vaccinated in 2010, up from 5% in 2008…
  • Medpage Today Parents increasingly say they are worried about the safety of the human papillomavirus (HPV) vaccine and don’t intend to vaccinate their teen daughters… But there is no similar pattern for two other vaccines aimed at adolescents…
  • CNN Health Concerns of mothers and fathers about the safety of the HPV vaccine grew each year, from 4.5% in 2008 to 16.4% in 2010… The number of parents who said they would not vaccinate their children for HPV increased from 38.9% in 2008 to 43.9% in 2010. The main concern was safety.
  • CBS News One of the main reasons parents said they didn’t want their children vaccinated against HPV was because of safety concerns.
  • Bloomberg The number of girls who received either injection (Gardasil or Cervarix) rose to about one-third in 2010 from 16 percent in 2008…
  • FiercePharma A growing share of U.S. parents say they won’t vaccinate their daughters… And that leaves Merck’s Gardasil and GSK’s Cervarix with a shrinking market.
  • The New York Timessuggesting, the need for interventions beyond clinical recommendations like possibly ‘state and federally designed social marketing campaigns.’… Without brushing aside the need to address safety concerns, the increasing rates of HPV vaccine refusal suggest that widespread vaccination will require more than marketing campaigns. Medical professionals need to look for ways to tell a better story to parents and teens about HPV, vaccination and cancer. (emphasis added)

Taxpayer funded social marketing campaigns? Look for ways to ‘tell a better story’ to parents? Who are these people kidding? What happened to investigative journalism? What happened to fact-finding? What happened to fair and balanced journalism?

Has no one considered the possibility that the 43.9% of parents refusing this particular vaccine might have some valid concerns? When will people realize there is a huge difference between ‘increasingly concerned about the safety’ and ‘increasingly aware of the potential risks’? After all, this would not be the first time a prescription medication approved by the FDA as ‘safe and effective’ turned out to be nothing of the sort. Will HPV vaccines be next?

HPV vaccination programs worldwide are based on two assumptions. First, HPV vaccines will prevent cervical cancer and save lives. Second, HPV vaccines will pose no risk of serious side effects. Therefore, it would make sense to vaccinate as many pre-adolescent girls as possible to reduce the worldwide burden of cervical cancer. What happens if both of these assumptions are not based on factual evidence?[1]

Medical Consumers Want to Know:

  1. Since HPV vaccines have never been shown to prevent cervical cancer, why are they being promoted as cervical cancer vaccines?1
  2. Since the majority of HPV infections and a great proportion of abnormal lesions associated with cervical cancer development clear spontaneously without medical treatment, how can these factors be used as ‘end-points’ during clinical trials to reliably predict the number of cervical cancer cases that could be prevented by HPV vaccines?1
  3. How can the clinical trials make an accurate estimate of the risk associated with HPV-vaccines if they are methodologically biased to produce false negatives?1
  4. Why are HPV vaccines marketed so aggressively in developed countries, when 85.5% of annual cervical cancer cases and 87.9% of annual cervical cancer deaths occur in developing countries?[2]
  5. How can passive adverse event monitoring systems (voluntary reporting with no penalty for failure to report), such as those used by most vaccine surveillance systems world-wide, allow the medical regulatory agencies to make accurate estimates on the real frequency of HPV-vaccine related adverse reactions?
  6. How can accurate estimates of the real frequency of HPV-vaccine related adverse reactions be made if appropriate follow-up and thorough investigations of suspected vaccine reactions are not conducted?

The FDA granted Merck’s HPV vaccine, Gardasil, fast track approval in June of 2006, despite the fact that this HPV vaccine failed to meet the FDA criteria for fast track approval.[3] FDA approval of GSK’s HPV vaccine, Cervarix, followed shortly after in January 2007.

According to The New York Times, the CDC Advisory Committee on Immunization Practices recommended adding HPV vaccines to the immunization schedule in the U.S. despite the fact that 64% of the advisory committee members had potential conflicts of interest which were either never disclosed or left unresolved at the time they voted. 3% of the members actually voted on matters they had been barred from considering by ethics officers. News like this certainly does little to enhance the level of public trust.

Is it possible for the FDA to objectively monitor the safety and efficacy of HPV vaccines? One has to wonder since Congress tightened the rules on outside consulting after similarly undisclosed conflicts of interest were discovered within advisory committees at the FDA.

As if this is not enough, the United States Department of Health and Human Services, via the National Institutes of Health, Office of Technology Transfer receives royalties on each HPV vaccine sold worldwide. This happens because technologies used in the production of HPV vaccines were developed at NIH and subsequently patented by them. For three of the last five years, HPV vaccines based on recombinant papillomavirus capsid proteins have ranked #1 based on royalties from product sales.[4]

Marketing Gardasil to the public under these circumstances is a typical case of unconstrained government self-dealing. The major patent holder (National Cancer Institute/NCI), the regulator (FDA) and the vaccination policy maker (CDC) are all divisions of the Department of Health and Human Services (DHHS). These self-dealings typically benefit some administrators, not the government or tax payers.  For example, Dr. Julie Gerberding, as the Director of the CDC, approved the use of Gardasil for cervical cancer prevention as a public health policy is now the president of Merck’s Vaccine division promoting the sales of Gardasil.

How much revenue is generated for the NIH from international sales of HPV vaccines? In November 2010, Dr. Eric Suba submitted a Freedom of Information Request to the Office of Government Information Services to discover the amount. It seems the financial details of the partnership between the NIH, Merck and GlaxoSmithKline are exempt from disclosure. (Read the response received here.) Apparently, transparency in government does not apply to the top 20 revenue producing patent(s) developed at taxpayer expense. Why is the public not allowed to share in celebrating the success of products they financed?

Three Strikes for Gardasil?

  1. September 2011: Recombinant HPV DNA L1 gene DNA fragments, possibly attached to the aluminum adjuvant, were discovered in 100% of Gardasil samples tested. There was no subsequent investigation. The FDA simply declared the ‘expected’ presence of residual DNA is not a safety factor. No documentation was provided. The fact that HPV vaccines were approved by governments worldwide based on manufacturers’ assertions that the vaccines contained ‘no viral DNA’ was completely ignored.[5], [6] The possibility of recombinant HPV DNA fragments being attached to aluminum adjuvant particles was also ignored.
  2. August 2012: One of the antigens used in Gardasil was discovered in central nervous system samples from two girls who died after being vaccinated with Gardasil. No cause of death was identified upon autopsy in either case.[7] HPV-16 L1 gene DNA fragments of vaccine origin apparently attached to aluminum adjuvant particles were also discovered in post mortem blood and spleen samples of a girl who died 6 months after Gardasil injections.[8], [9]
  3. February 2013: It was discovered that the naked HPV 16 L1 gene fragments bound to aluminum particles by ligand exchange in Gardasil have acquired a non-B conformation. This conformational change may have stabilized the HPV 16 gene fragments in Gardasil preventing their normal enzymatic degradation in vaccine recipients.[10], [11] Non-B DNA conformations and their relationship to diseases has been studied since the 1960’s. Based on current scientific knowledge, the human genetic consequences of these non-B DNA structures are approximately 20 neurological diseases, approximately 50 genomic disorders and several psychiatric diseases.[12], [13] The impact of injected foreign non-B DNA on human health is totally unknown. 

Why have none of these discoveries sparked a single investigation in any country? Why is no one concerned when genetically modified viral DNA fragments are found in vaccines that are reported to have no viral DNA? Why is no one worried about those viral DNA fragments being attached to aluminum (a known toxin) possibly creating a new chemical compound of unknown toxicity? Why are no red flags raised when those viral DNA fragments attached to aluminum acquire a non-B conformation – something known to be associated with multiple debilitating diseases? Anyone with an ounce of common sense should demand to know why those charged with approval, recommendation and safety monitoring of these vaccines appear to be utterly unconcerned about the future health implications of any one of these discoveries, much less all three of them.

What kind of ‘expert’ advice is being given to YOUR government health officials?

Israel’s Advisory Committee on Infectious Diseases and Inoculations held a teleconference on 30 January 2013, to discuss the proposed introduction of HPV vaccines into the country’s school inoculation program among other issues. The official transcript of that meeting, dated 11 February 2013, provides some interesting insights for medical consumers who question HPV vaccine safety.

Ron Dagan, MD, is Professor of Pediatrics and Infectious Diseases at the Ben-Gurion University of the Negev in Beer-Sheva, Israel, and Director of the Pediatric Infectious Disease Unit at the Soroka University Medical Center, also in Beer-Sheva. An active researcher and international lecturer, Dr. Dagan’s work focuses on new conjugate vaccines. His expert advice to Israel’s Advisory Committee regarding potential HPV vaccine implementation is as follows (translation provided-emphasis added):

We are dealing with injections, some of which given in 3 [separate] doses, which are delivered to teenage girls. Many side effects are to be expected. During the week following the vaccine delivery of the injections many serious events which are not related/linked to the vaccination are expected: fainting, deaths and convulsions/fits. This needs to be taken into account. Even if it is not rational, if these events happen in class they may damage the general perception/status of the vaccinations. This is happening all over the world all the time. We have already dealt with a similar issue in relation to the delivery of MMR with TD and Polio and we have accepted the nurse’s proposal to split these between grades 1 and 2. The nurses are suitable to make recommendations to the committee in relation to this issue. In relation to the side effects, we need to be prepared in advance and not simply react after the fact. I propose we consult with the English representatives as to how they’ve gone about this. We must prepare for the delivery of the new vaccine. The nurses need to know they are going about this in the way they are most comfortable with (/have the most control over/familiarity with).

If this is an example of the expert advice vaccination programs are based on, it’s no wonder medical consumers are questioning HPV vaccine safety, efficacy and need. Many side effects are to be expected? Fainting, deaths, convulsions and fits occurring during the week following vaccination – yet not related to the vaccine? Preparing in advance for side effects? Consulting with other countries to see how they handled the problem? Are countries around the world being offered similar expert advice?

So, what will it take to solve the HPV vaccine uptake problem?

Parental concerns about HPV vaccine safety are not going to go away in response to social media campaigns. Teaching medical professionals to ‘tell a better story’ is not going to make parents change their mind about Gardasil, Cervarix, or any future HPV vaccine. Platitudes and unsubstantiated reassurances are no longer sufficient.

The time has come for government health authorities to make HPV vaccine manufacturers prove their claims or pull their products from the market. Medical consumers want scientifically proven facts – Safe, Affordable, Necessary and Effective – nothing less is acceptable.


The above article is from SaneVax.org and was written in 2013. This information is still valid and a reminder is in order for the current fight for our rights around the country and in RI about the HPV vaccine. #InformedConsent is essential and very important points are not being disclosed.

Since this article was published, last month there was a change in the dosing scheduled suggestions by the CDC. Where children under age 15 only need to receive two doses vs three doses. More specific details also apply.

Now on Nov 18th the CDC will hold a training to teach health care workers how to encourage the HPV vaccine and how to understand the new dosing recommendations by the CDC from Oct 2016.

Share this blog post with your legislator and schedule a time to sit down and speak with them.

VICP has paid out nearly 6million in claims to HPV vaccine injury victims

VICP has paid out nearly 6million in claims to HPV vaccine injury victims

Documents Obtained by Judicial Watch Reveal 200 Claims Filed with HHS for HPV Vaccine Injuries and Deaths, 49 Compensated 

Documents Reveal that the National Vaccine Injury Compensation Program (VICP) has Paid Out Nearly $6 million in Claims to Victims of Controversial HPV (human papillomavirus) Vaccine, including Families of Two Dead

(Washington, DC) – Judicial Watch announced that it has received documents from the Department of Health and Human Services (HHS) revealing that its National Vaccine Injury Compensation Program (VICP) has awarded $5,877,710 dollars to 49 victims in claims made against the highly controversial HPV (human papillomavirus) vaccines. To date 200 claims have been filed with VICP, with barely half adjudicated.

The documents came in response to a February 28, 2013, Judicial Watch lawsuit against HHS to force the department to comply with a November 1, 2012, Judicial Watch Freedom of Information Act (FOIA) request (Judicial Watch v. U.S. Department of Health and Human Services (No. 1:13-cv-00197)). On March 12, 2013, The Health Resources and Services Administration (HRSA), an agency of HHS, provided Judicial Watch with documents revealing the following information:

  • Only 49 of the 200 claims filed have been compensated for injury or death caused from the (HPV) vaccine.  Of the 49 compensated claims 47 were for injury caused from (HPV) vaccine the additional 2 claims were for death caused due to the vaccine.
  • 92 (nearly half) of the total 200 claims filed are still pending.  Of those pending claims 87 of the claims against (HPV) vaccine were filed for injury, the remaining 5 claims were filed for death.
  • 59 claims have been dismissed outright by VICP.  The alleged victims were not compensated for their claims against the HPV vaccine.  Of the claims dismissed, 57 were for injuries, 2 were for deaths allegedly caused by the HPV vaccine.
  • The amount awarded to the 49 claims compensated totaled 5,877,710.87 dollars. This amounts to approximately $120,000 per claim.

VICP is a Health and Human Services program that compensates patients who have been adversely affected by certain vaccines. The HHS web site describes the program as a “no-fault alternative to the traditional tort system,” and it covers 16 specific classes of vaccines, including HPV vaccines which were added in 2007.

From its inception, the use of HPV (human papillomavirus) vaccines for sexually transmitted diseases has been hotly disputed.  According to the Annals of Medicine: “At present there are no significant data showing that either Gardasil or Cervarix (GlaxoSmithKline) can prevent any type of cervical cancer since the testing period employed was too short to evaluate long-term benefits of HPV vaccination.”

“This new information from the government shows that the serious safety concerns about the use of Gardasil have been well-founded,” said Judicial Watch President Tom Fitton.  “Public health officials should stop pushing Gardasil on children.”

In addition to obtaining records from the FDA through the agency’s Vaccine Adverse Event Reporting System (VAERS) which has documented thousands of adverse reactions to Gardasil, Judicial Watch also published a special report in 2008 detailing Gardasil’s approval process, side effects, safety concerns and marketing practices.

 

STOP THE MANDATE IN RI FOR THE HPV VACCINE, donate to help the fight. This is coming across the country. Help RI show the country that we all will band together against the mandate of HPV vaccinations. www.gifts.nohpvmandateri.com Donate $10 Today.

Sign the petition to advocate for informed consent and reverse the HPV vaccine mandate in RI.

 

 

Article dated March 2013