A Montreal social scientist and the federal agency that awarded her almost $300,000 to study the HPV vaccine are facing criticism after the professor condemned the vaccine and called for a moratorium on its use. Concordia University’s Genevieve Rail also said there is no proof that the human papillomavirus directly causes cervical cancer.
October is deemed the start of the flu season. This year, the rhetoric and methods to push flu vaccines are beginning to take on an authoritarian flavor. Medical consent and medical choice appear to have taken a backseat to government mandates and strong arm tactics by local pharmacies, medical practitioners, and employers. Government oversight bodies and medical professionals are omitting the risks and informed consent when it comes to the flu shot. To understand this year’s flu vaccination push, here are some points to put things into focus.
What happens when a potential blockbuster vaccine (Gardasil, Cervarix, or Gardasil 9) is simply not accepted by the public on the same level as other recommended vaccines? Do the manufacturers and international health authorities re-examine the product to assess whether or not public concerns are valid? Not often, and when they do it is pretty much a cursory ‘investigation’ where they are quite careful to NOT look in the direction needed to expose any potential problems. What is wrong with this picture? Could it have anything to do with the fact psychologists and psychiatrists have been studying how to manipulate public behavior for over 35 years? Could the results of these studies be used by HPV vaccine promoters to manipulate the public, medical professionals and/or politicians to increase the uptake of HPV vaccines?
Senator Paschal Mooney calls the Irish HPV vaccination program a national disgrace condemning the national health authorities for ignoring the basic right to informed consent and ignoring pleas for answers from families affected by adverse health after Gardasil injections. He is putting forth a resolution aimed at forcing the HSE (national health agency) to meet with affected families and answer their questions. He also mentions how the packet insert for the Gardasil vaccine lists 21 side effects, and that this information is not being passed on to the parents and girls between 12 and 17 years of age before deciding whether or not to receive the vaccine.
When a woman becomes pregnant, naturally, she would want to protect her unborn child above all else. Therefore, when offered a series of vaccinations said to protect her newborn baby against disease in the first few weeks of life, she will probably accept the vaccinations without a moment’s hesitation. However, would she accept those vaccinations so readily if she knew that her unborn child was going to be used as part of a vaccine experiment being conducted by the Centers for Disease Control and Prevention (CDC) and the vaccine manufacturers? Health Impact News decided to investigate this issue more carefully, and what we uncovered may shock and horrify you.
The United States continues to carelessly move forward with the HPV vaccine Gardasil. Meanwhile, due to its endless damage, the shot is the center of criminal lawsuits in Spain, India, France, Japan and many other countries. In the UK, the HPV vaccination push has 8,228 official reports of side-effects, almost more than all other vaccine reports combined. Dr. Dalbergue, a former pharmaceutical industry physician with Gardasil manufacturer Merck gave a 2014 interview stating that: “Gardasil is useless and costs a fortune” as well as predicting “Gardasil will become the greatest medical scandal of all times…” Ignoring data and worldwide protest, Departments of Health within the U.S. are now sending letters to parents advising them to submit their children to HPV vaccinations. With no prior announcement, parental consent given, or notice, the states of New York and Indiana have tracked HPV vaccine non-compliers and are now hassling them with physical letters.
According to the Center for Disease Control and Prevention’s (CDC) own statistics, the seasonal flu vaccine for the 2014-2015 season was only 19 percent effective. So why is there a worldwide push for flu vaccination? What are the risks inherent in a flu vaccination and are they worth it? These questions have been deleted, ignored, omitted, and crossed out by most in favor of what appears to be a dose of drug company profit mixed with political agenda.
U.S. government officials and agencies have proven that they cannot be relied upon to give the public accurate information regarding vaccine safety and efficacy. With the National Vaccine Compensation Program implemented in 1986 to grant pharmaceutical companies total legal immunity allowing them to put as many vaccines into the market place without the threat of lawsuits if they harm or kill people, the incestuous relationship between Big Pharma and government agencies overseeing vaccines has become a huge conflict of interest. One of the most controversial vaccines world wide is the HPV cancer vaccine. Young girls are suffering tremendously, many of them experiencing premature menopause and with no hope of ever starting their own families. The official U.S. government response has been that there are no problems with this vaccine, and that it is totally safe. Other countries are not obligated to continue promoting this propaganda, and there are many lawsuits currently in litigation in Europe. Japan is one government that has taken a more sane approach to the HPV vaccine, and is still investigating the harmful effects, while leaving it an optional vaccine that they do not officially endorse. In addition, they are exploring ways to help the victims who have suffered from the vaccine.
California Senate Bill 277 (SB277) is setting a dangerous precedent by removing medical consent from California school children in 2016. In addition, the bill appears to be in violation of the Nuremberg Codes for informed medical consent. However, pressure is already being felt as school administrators and directors have chosen to ignore current law and force vaccine schedules on school children. The language of SB277 left enforcement and vaccine noncompliance up to the school’s governing authority for each district. Orange County’s Department of Education’s Legal Division interprets that a court order to vaccinate will be an option. Will all California school districts, by way of their legal counsels, be directed to file court orders against noncomplying parents of all school children in 2016? It is essential that all California parents that believe in medical freedom file a personal belief vaccine exemption before the January 1st deadline. This is the only method known at this stage to grandfather a waiver into your child’s 2016 school year.
The National Vaccine Information Center stands in solidarity with parents who are gathering in Atlanta and witnessing about what happened to their once healthy children, and are again calling on the CDC to tell the public the truth about vaccine injuries and deaths. We stand with in solidarity with all who want to protect the right to know and the freedom to choose how to stay healthy in America. Be in Atlanta October 24, 2015 To Stand Up at the Truth, Transparency & Freedom Rally!
Before Gardasil my daughter was an outgoing, super funny, confident, soccer athlete, practicing 3-4 hrs a day. She planned to play HS soccer and move on to college soccer. Autumn was a free spirit and so full of life. Her love for animals and passion to save the mistreated drove her to want to open her own animal shelter. She had dreams, goals and a plan. That is until she had the Gardasil vaccine. Autumn fought hard to keep the life she had prior to Gardasil, but eventually was forced to quit soccer and withdraw from school. She has been diagnosed with depression and anxiety. Autumn suffers from extreme memory loss, anger, insomnia, and severely diminished cognitive processes. She has self-harmed, cutting and branding her wrist/hips to cope with the suffering she endures daily. Did the benefits of Gardasil outweigh the risk for Autumn? Absolutely not!
The non-profit National Vaccine Information Center (NVIC) is questioning the basis for the fast tracked licensure by the U.S. Food and Drug Administration (FDA) of a squalene-adjuvanted influenza vaccine for use in seniors over age 65. The Novartis MF59 adjuvanted Fluad vaccine was approved for accelerated licensure by the FDA Vaccines and Related Biological Products Advisory Committee (VRBPAC) on Sept. 15, 2015 primarily using limited immunogenicity and safety evidence from a small clinical trial in which only about 1,000 healthy Americans over age 65 were given the adjuvanted vaccine. Although MF59 is bioactive and designed to stimulate a strong immune response, FDA does not require that vaccine adjuvants be proven safe in a placebo controlled trial and they are not licensed separately. Fluad will be the first influenza vaccine licensed in the U.S. containing squalene, a controversial oil in water adjuvant that has been linked with development of autoimmunity, narcolepsy and other immune and neurological disorders.
Scientists state that there have been no cases of wild polio reported in four out of the six regions of the world being targeted in the vaccine-program since the 1990s, and the only cases of polio that are being reported are those of VDPV caused by the OPV vaccination. The oral polio vaccine was banned from use in the United States in 2000. The reason for this ban was because too many children were developing vaccine associated paralytic polio (VAPP) as a serious side effect of the oral vaccine. When you hear about 'outbreaks' of polio in foreign countries, the first question you should ask is, 'Are they using the oral polio vaccine?' and the answer is usually, 'yes.' If children in the US were getting VAPP as a significant side effect of the oral vaccine, why wouldn't this occur in other countries where children are receiving the oral polio vaccine, and health conditions may actually be worse for them there, than they are in the US? It has been proven over and over again that vaccinations alone cannot eradicate polio. Isn’t it about time that governments stopped their lies and got their priorities right for the sake of innocent children?
Due to dwindling capacity for existing aborted fetal cell lines to self-replicate, scientists in China have developed a new aborted fetal cell line, WALVAX 2 that will be used for viral vaccine production. The existing cell lines, MRC-5 and WI-38 are currently used in MMR, Varicella, Hepatitis-A, Shingles, some rabies and some polio vaccines. WALVAX 2 is taken from the lung tissue of a 3 month gestation female who was ultimately selected from among 9 aborted babies. The scientists noted how they followed specific guidelines to mimic WI-38 and MRC-5 in selecting the aborted babies, ranging from 2-4 months gestation. They further noted how they induced labor using a “water bag” abortion to shorten the delivery time and prevent the death of the fetus to ensure live intact organs which were immediately sent to the labs for cell preparation.
I am 16 years old. For me, everything started a few days after I received the HPV vaccine, Gardasil. I woke up one day choking and unable to breathe. I felt like I was going to pass out so my parents took me to a hospital. I was stabilized, kept overnight and sent home, just like that. No tests, no medications, no explanations as to what could have caused the problem. This was only the beginning. Then it progressed to choking, hyperventilating, panic attacks and soon enough I was getting panic attacks every day, sometimes as many as four times a day. Then the depression came. Every doctor we went to dismissed us and tried to get rid of us. I genuinely had to force myself to want to live. I wanted to disappear. I wanted all of the symptoms to stop.
With military precision, the Centers for Disease Control (CDC) announced at an Aug. 27, 2015 press conference that national vaccination rates among young children in the U.S. continue to be very high but that more must be done to tag and track down children without every government recommended vaccine and publicly shame schools that fail to maintain a 95% plus vaccine coverage rate. Government health officials partnering with industry have declared war on citizens exercising freedom of thought, speech and conscience, who question the safety and effectiveness of government vaccine policies and defend the human right to informed consent to medical risk taking. Military strategies employed to win wars view casualties as necessary losses. Unfortunately, it appears that those waging the “take no prisoners” culture war view both the vaccine injured and human and civil rights as necessary losses.
NVIC regularly monitors meetings held by federal vaccine advisory committees, including the Advisory Commission on Childhood Vaccines (ACCV) and the National Vaccine Advisory Committee (NVAC). In recent years, information about compensated vaccine injury claims published in the VICP Data and Statistics Report has changed - but not for the better. This report prepared by DHHS officials continues to provide limited insight into vaccine injury and death awards, despite the fact that federal law states the public has a right to additional information, much of which is presented in bits and pieces during ACCV meetings. While DHHS gives some of this information to the ACCV on a quarterly basis, the information is not as meaningful as it could be because of the way it is presented in ACCV meetings and on the VICP’s website. There is no ability for the public, or the ACCV for that matter, to connect the dots between vaccine injuries compensated by vaccine and condition over time, or to determine the reasons and any associated trends on why petitions are dismissed and claimants are denied compensation.
President Ronald Reagan signed The National Childhood Vaccine Injury Act (NCVIA) of 1986, absolving drug companies from all medico-legal liability when children die, become chronically ill with vaccine-induced autoimmune disorders or are otherwise disabled from vaccine injuries. That law has led directly to an expected reckless, liability-free development of scores of new, over-priced, potential block-buster vaccines, now numbering over 250. The question that must be asked of Big Medicine’s practitioners: How will the CDC, the AMA, the AAFP and the American Academy of Pediatrics fit any more potentially neurotoxic vaccines into the current well-baby over-vaccination schedule? PhRMA (the Pharmaceutical Research and Manufacturers of America), the pharmaceutical industry’s trade association and powerful lobbying group, says that: "today, more than 7,000 medicines are in development globally, all of which have the potential to help patients in the United States and around the world. According to another data source, there are 3,400 medicines in development today just in the United States, an increase of 40 percent since 2005." PhRMA also says that today: "the 271 vaccines in development span a wide array of diseases, and employ exciting new scientific strategies and technologies. These potential vaccines – all in human clinical trials or under review by the Food and Drug Administration (FDA) – include 137 for infectious diseases, 99 for cancer, 15 for allergies and 10 for neurological disorders." Whenever the FDA signals that it is ready to grant marketing approval for a new vaccine or drug, the first step for the pharmaceutical company’s marketing department is to promote an “educational” advertising campaign designed to instill fear in parents (and their pediatricians) about the horrible illnesses (albeit previously unknown, benign or rare) that even us doctors hadn’t yet recognized as being significant up until recently. Most of us physicians have gone along with the fear-mongering that makes our practices busier while it also makes billions of dollars in profits for some unworthy CEO or Wall Street investment banker, hedge fund manager or mutual fund investor – all at the expense of America’s precious and vulnerable children who are at high risk of being sickened along the way.
My daughter was born on December 6, 1999. She was approximately 14 years, and 2 months old when she first suffered an adverse reaction to a vaccine. J.G. was a happy, very healthy, normal, teenage girl. All that changed when the doctor in her pediatrics office recommended she receive Gardasil as prevention against cervical cancer. J.G. has lost her teenage years due to her debilitating condition, and cannot live a normal life. The fear of bruising and her potentially low platelet count dominates her mind wherever she goes. No child should have to go through what my daughter has experienced.
Dr. Michelle Davis has become the latest extremist pro-vaccine doctor to propose removing parental choice regarding vaccines, by eliminating the philosophical and religious exemptions currently in place by law in the State of Michigan. As we have previously reported here at Health Impact News, most of the nations doctors do NOT hold the extremist pro-vaccine view that ALL vaccines are safe ALL the time for EVERYONE and should be given to ALL children, by force if necessary. This is an extremist position, and most physicians, whether in the "pro-vaccine" or "anti-vaccine" camp fall far short of this position. Attempts by the pharmaceutical lobby to pass legislation that takes away these parent choices have failed in every state so far, except California. In California, SB277 was passed in spite of massive opposition by both parents and doctors due to a strong pharmaceutical lobby and massive funding in that state. Will the parents of Michigan and other non-extremist medical professionals allow Michelle Davis to force her extremist views on the rest of the State of Michigan?
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