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

 

 

Thank you for supporting Rhode Islanders against mandated HPV vaccinations
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Need Volunteers this week

Need Volunteers this week

Hello Supporters of Rhode Islanders against mandated HPV vaccinations;

This week we will be in attendance at two events and one of those events we need volunteers to help spread awareness. The second event we invite you to attend as Aimee Gardiner our Director speaks about the fight in RI against the mandate.

RI Kids Consignment Sale is happening this week. Thurs, Sat, and Sun. Can you help be with the table to share info and ask for signatures on our petition? You do not need to feel like you have to know all the facts to help. There will be printouts to reference and hand out, but having a person to see at the table and be able to say “thank you for taking a look at the info” can make a huge difference to parents that are not aware of the issue.

Sept 29-Oct 2 ~~ Thurs 9:30a-5  Sat 9:30a-3  Sun 8:45a-12

Can you help with any of these times, or part of the day vs the whole day? Thurs is a day that we could really use the help with the shift of 9:30a-2:30p. Please call Aimee at 4014062647 or email aimee@nohpvmandateri.com to volunteer.

You are invited to attend “For the Love of Freedom” hosted by Adam Kokesh on Sept 30th Friday at 7pm in Warwick. Aimee will be speaking at this event and there will be info about different ways in RI you can connect with groups that are fighting for a cause and standing up against government overreach. The event is being held at the Firefighter’s Hall, 750 Warwick Ave in Warwick.

The CDC group; The ACIP is having a quarterly meeting that involved the HPV vaccine. We sent an email a couple days ago in regards to submitting public comment to be recorded in the meeting. Please submit comment by Sept 29th it only takes 3or4minutes.

Have you subscribed to our Facebook events to get notified of new ones posted immediately? https://www.facebook.com/RIagainstHPVmandate/events

If you are not able to help at any of the times this week, (even if you are helping too) please share the RI HPV Info pack with others. Via social media and printing a couple copies and placing on a library bulletin board or coffee shop. The direct link is http://www.RIHPVinfo.nohpvmandateri.com

 

Thank you so much for all the help and support through out the year.

 

ACIP Meeting will address HPV vaccine, ACT NOW

ACIP Meeting will address HPV vaccine, ACT NOW

The ACIP of the CDC is having a quarterly meeting that will address vaccines, one of the ones that will be specifically discussed, is the HPV vaccine.

Public comment only has one more week to be submitted and counted to be documented in public record of meeting. The TIME IS NOW to speak up directly to the CDC in this fight of the HPV vaccine and having the right to informed consent privately with family doctor.

We suggest the following points in your written comment to ACIP. Below you will find the exact instructions for sending this comment and what information is required to submit with comment.

  • Concern was publicly raised about ovarian failure related to the HPV vaccine. This should not be ignored and further detailed studies should be done immediately, and prior to more vaccines being recommended.
  • Advertising the HPV vaccine for cancer prevention should cease immediately. Not one study proves cancer prevention, it is an assumed result that does not have solid proof yet. This is extremely misleading to the public and does not permit proper informed consent.
  • CDC should cease and desist on any form of advertising of any vaccines to the public. Vaccine manufacturers are free from liability when a vaccine causes a negative side effect. They benefit full profits of all vaccine sales. Our tax dollars and government agencies should not be paying to advertise a product that produces billions in profits for the manufacturer.
  • Multiple countries are no longer recommending the HPV vaccine due to a high level of young adults having serious side effects of the vaccine. The CDC and ACIP need to take this seriously and show the US public that they do care about the youth, and will also do more follow up studies and further investigation of the HPV vaccine.

 

About ACIP Meetings

The Committee meets three times annually at the Centers for Disease Control and Prevention (CDC) in Atlanta, Georgia. Meetings are open to the public and available online via webcast. During the meetings, members and CDC staff present findings and discuss vaccine research and scientific data related to vaccine effectiveness and safety, clinical trial results, and manufacturer’s labeling or package insert information. Outbreaks of vaccine-preventable disease or changes in vaccine supply, such as vaccine shortages, also are reviewed during meetings.

Deadline: SEPTEMBER 29TH 2016
10 workdays before the meeting. Meeting Scheduled for Oct 19th
Content of written comments:
  • •name
  • •address
  • •organizational affiliation
  • •e- mail address of the speaker
  • •topic being addressed
  • •specific comments
Format and length of written comments:
  • •Must not to exceed one single-spaced typed page with 1 inch margins containing all items above.
  • •Only those written comments received 10 days in advance of the meeting will be included in the official record of the meeting.
Contact:
Stephanie Thomas, CDC, NCIRD. Email ACIP@cdc.gov

 

ACIP (Advisory committee on immunization practices)

October Meeting is Oct 19-20 (Mark your datebook to watch this live)

Live Webcast Instructions
Advisory Committee on Immunization Practices (ACIP)
Centers for Disease Control and Prevention (CDC), Atlanta, GA
Oct 19: 8:00 am – 6 pm
Oct 20: 8:00 am – 3:30 pm

  1. Due to Firewall concerns, some users may need to cut and paste the link into their internet browser.
  2. Closed Caption are only available on the Windows Media link.

Windows Media Link ~~~~~~~~ Flash Link

Meeting Agenda — HPV VACCINE IS ON THE AGENDA

Listening to meeting via phone only:
Toll Free: 1-877-925-7916
Passcode: 4080878459

Join the Facebook event and select “going” to get the reminders and to share with others to make their voice heard too.

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

1yr Rally Anniversary

1yr Rally Anniversary

1 year ago today Rhode Islanders against mandated HPV vaccinations partnered with the Center for Freedom and Prosperity held a joint rally in Cumberland RI, as the first public appearance of the stand against the mandate and to advocate for informed consent.

Many RI citizens showed to support the efforts of reversing the mandate and four legislators were there from the very start. Justin Price, Elaine Morgan, Bobby Nordolillo, and Blake Filippi. Sherry Roberts was not in attendance of the Rally but was vocal in her support.

What has happened since?

  • #NOHPVmandateRI partnered with the Gaspee Project a 501 c4
  • We held “Making Waves in the Ocean State” and had a wonderful event where Brandy Vaughan, and Toni Bark flew in to speak to us, and many local doctors and legislators contributed to the evening also.
  • The petition has reached close to 3000 signatures and is still growing.
  • FIVE bills were introduced in the 2016 legislative session to support the efforts that parents in this have been advocating for.
  • Many new candidates running for office have voiced their support of the Rhode Islanders against mandated HPV vaccinations and that the mandate should be reversed.
  • The RI Dept of Health decided to kick up their efforts ( we are pretty sure they have never been challenged to this degree before) to increase vaccination rates vs respecting parents right to choose for their families. So your tax dollars have been spent on direct mailing to minors and robo calls to homes to get the HPV vaccine this summer.
  • The Awareness Campaign kick off this summer to counter the Dept of Health with informed consent, to be sure parents know the options they have a right to and both risks vs benefits without a one sided story. To hold legislators accountable that will not support protecting the right to make medical decisions for your child, especially ones that do not impact the classroom and should have nothing to do with attending school. YOU CAN HELP THIS EFFORT DONATE TODAY.

We have not stopped working and educating on this topic, and are excited to celebrate a year of hard work and dedication. Thank you so much for your support, whether you were with us from the start or recently joined. Our work is not over, and many more still need to know this fight is happening. Be sure to share with others, use social media, call your closest family and friends, forward an email from us, and especially donate to the cause. Donate $15 or more Now and show your state representative and senator you mean business.

Enjoy the photo memories from Aug 17, 2015 Rally

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Do you want to be more involved? Do you have questions?

Please feel free to email changehpvmandateri@gmail.com  or comment here on the blog post.

 

Judy Mikovits PhD and the HPV vaccine

Aug 13 2016 Judy Mikovits presents on the HPV vaccine and the study data associated with it.

 

This webinar was just recorded today 8-13-16, and hosted by FactsOnVax- this video is almost 2 hours long, and may only be available for 72hrs.

May 2016 Director of Rhode Islanders against mandated HPV vaccinations; Aimee Gardiner, also did an interview with Dr Nancy Tarlow, please take a look at that blog post too.

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

Donate to help fight the RI Dept of Health and the state general assembly to overturn this mandate and put the power of total private choice back in the parent’s hands. PLEASE DONATE TODAY

Action needed now, August 2016

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Right now, we need to advocate for informed consent and be sure parents know their rights. This fall, we must hold lawmakers accountable for their votes and actions. This fall we need to send a clear message that if elected officials support policies that benefit the special interests – instead of the people of Rhode Island – that we refuse to be silent. That we will campaign against the RI Dept of Health’s lack of transparency, and we mean business.

We must protect the rights of Rhode Island parents to make choices about our own children’s health. The HPV Vaccine Mandate robs us of this right and puts the government between us and our doctors. Even more disturbingly, the RI Department Of Health is now using your tax dollars to market the vaccine directly to our children – bypassing you, their parents.

As you know, our anti-HPV mandate movement has partnered with The Gaspee Project to raise awareness and money. Now is the time to support our cause.

By clicking the link below and making a donation, you will help us build our campaign war-chest so that we can make independent expenditures in select upcoming General Assembly races, and inform parents of their options.

 

Please give your most generous contribution today!

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Share this message with friends and family too.

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