As political races continue to heat up, be aware of the candidates from the presidential level down to your county officials and where they feel the government's role should be in health care. Experience shows that the more control the government has over your health care, the less freedom you will have, period. Don't forget that WITH OUR TAX DOLLARS - our FDA approved the HPV vaccine, our Congress gave the vaccine maker liability protection from the harm caused by this vaccine, and some of our state legislators and governors have tried to FORCE this vaccine on our young daughters. Look at these articles and ask yourself how much more you want the government deciding for you what you must do to be healthy. Find some candidates you believe in and help them. Our lives depend on it.
"She was walking through my house and collapsed. She told me she couldn't feel her leg. We went right to the hospital," says Christina Bell, Brittany's mom.
Bell says there were no answers at first, but then she started to put the pieces of the puzzle together.
Two weeks before her daughter's collapse, Brittany received her first injection of a vaccine called Gardasil.
"The doctor recommended we get the Gardasil shot and I'd been thinking about it because I've seen it on TV all the time," says Bell.
The virus causes 70 percent of cervical cancer.
Over the last year, the vaccine has been the center of moral controversy, but little has been mentioned about the number of vaccine reactions reported to the FDA.
Recent news reports link an association with paralysis and death with the vaccine.
"The reason I'm skeptical with this is this isn't a virus," says Dr. Guy Benrubi, an OB/GYN with Shands.
Dr. Benrubi says the HPV vaccine is one of the safest and he recommended it to his own child.
"The immediate risks are minimal. The FDA looked at those. We have not seen any major catastrophes," says Dr. Benrubi.
Benrubi says the majority of complaints are patients fainting during or after the shot.
So far, more than four million vaccinations have been done and nearly 4,000 adverse reactions have been reported.
"Even the worst case scenario, if you have four thousand in four million that is a one to one thousand potential adverse effect," says Dr. Benrubi.
The list of complaints range from temporary blindness, blurry vision, convulsions, seizures and numbness in arms and legs that won't go away.
"If you know something is happening why do you let it continue?" asks Bob Giuliano, Brittany's grandfather.
Giuliano and his daughter want answers as to how they didn't know paralysis could be a possibility for Brittany.
"I am very angry," says Brittany's mom. Two months later and after hours of physical therapy,
Brittany still has no feeling in her left leg.
Getting around is difficult. It's hard for Brittany to walk and balance and she often needs a little help.
"She's mad. I can tell she's mad," says Brittany's mom. A little shy, Brittany did not want to talk to us, but she did want her story told so parents and young girls know how her life has changed.
Now she is learning to cope with braces, crutches and a walker. "It's changed everything for us," says Bell.
Brittany's doctors have diagnosed her with Acute Demyelinating Encephalomyelitis or ADEM.
It is an inflammation of the brain that has been associated with a vaccination.
"I think there is a little cart before the horse going on here. I'm not saying this is not a good vaccine, but anyone who is going to have their daughter or child have this shot, they need to be fully informed of risks or potential risks associated with it," says Sean Cronin, Brittany's attorney.
Cronin says he can't go after Merck with a lawsuit because Gardasil is now part of a federal fund which pays out to those injured from vaccines.
First Coast News has learned, Gardasil was added to the National Vaccine Injury Compensation Fund just months after it hit the market. "The Federal government would not put it on the list without medical scientific justification," says Cronin.
Brittany's family is filing an injury claim with the government.
They are also on a mission to spread the news of what they say can happen with the vaccine.
The family also holds out hope that one day, old Brittany will be back walking and running like she did once before.
"I do wish the doctor would have known and would have said there is a chance that this could happen. If he would have said, I would have never done it," says Bell.
Merck told First Coast News it is unaware of Brittany's case. Merck also says it actively monitors the adverse reaction reports and other databases throughout the world.
As for the vaccine being added to the government vaccine fund, Merck says it is their understanding that all new vaccines are added to the fund.
The Pharmaceutical giant says the latest numbers show that ten million HPV vaccines have been given in the United States.
15-year-old Marissa Omon is an athlete. The daughter of a Nigerian soccer player she played basketball, volleyball and track, until now.
Surgeons put a defibrillator inside her chest Monday night fearing her heart could stop at any moment.
"HPV cost my daughter. It almost cost her her life," said Edem Omon.
Edem Omon is convinced his healthy, athletic teenage daughter Miranda almost died because of a vaccine doctors gave her to prevent cervical cancer.
Three weeks ago Miranda took a physical. Edem said he reluctantly allowed a doctor to give her the HPV vaccine.
"He convinced me the drug was safe," said Edem.
Less than three hours later, while practicing basketball at Free State High School, Miranda suddenly collapsed. Her heart stopped. Paramedics needed a defibrillator to revive her. Miranda was rushed to Children's Mercy where she spent several days unable to walk or talk.
They say they do not believe the HPV vaccine has anything to do with it.
"I do believe it's safe," said Dr. Scott Dattel.
Dattel is not Miranda's doctor but said he's never heard of any major side effects caused by HPV, only soreness and fever.
"HPV vaccine was thoroughly tested before the FDA approved it and I do think for that reason it is safe," said Dattel.
Miranda is still in Children's Mercy. If all goes well she could go home this week but doctors will not allow her to play competitive sports that she loves.
"20-Jun-2007: Information has been received - concerning a 17 year old female who in June 2007 - was vaccinated with a first dose of Gardasil. During the evening of the same day, the patient was found unconscious (lifeless) by the mother. Resuscitation was performed by the emergency physician but was unsuccessful. The patient subsequently died."
"12-Jun-2007: Information has been received - concerning a 12 year old female with a history of aortic and mitral valve insufficiency - who on 01-MAR-2007 was vaccinated IM into the left arm with a first does of Gardasil. On 01-MAR-2007 the patient presented to the ED with ventricular tachycardia and died."
"28-Aug-2007: Initial and follow-up information has been received from a physician concerning an "otherwise healthy" 13 year old female who was vaccinated with her first and second doses of Gardasil. Subsequently, the patient experienced paralysis from the chest down, lesions of the optic nerve. At the time of the report, the patient had not recovered."
"In light of this information, it is disturbing that state and local governments might mandate in any way this vaccine for young girls," said Judicial Watch President Tom Fitton. "These adverse reaction reports suggest the vaccine not only causes serious side effects, but might even be fatal."
SOME FACTS ON THE GARDASIL VACCINE:
How safe is Gardasil? ( extracted from the Immunise Australia literature)
It is a frustrating time when our young girls and women are being lined up and jabbed with a vaccine that has the potential to affect their future fertility - HPV (Gardasil) vaccine - and that may be the least of the problems. Anyone with a HPV infection (and they are common), who is given the vaccine risks immune system shutdown or autoimmune disease. "Purpura vaccinatoria" - an abnormal immune system response has been recorded following vacination with smallpox and other vaccines when the vaccine recipient is already incubating the same infection. They are not testing for wart virus infection prior to vaccination. In the trials for this vaccine they were careful to exclude anyone with a wart virus or who developed a wart virus infection. They chose women who were not likely to have more than one sexual partner, thereby minimising this risk. THIS IS AN UNKNOWN RISK FACTOR but when you read the reports already in from overseas you will see that once again vaccination is not rocket science, unless you equate it with the ones that explode and obliterate!
Please pass on the following information and contact VISA for articles and flyers
"Your daughter may experience minor side effects such as redness, pain, swelling at the injection site and mild fever. (and the rest?)
She should not have the HPV vaccine if she is pregnant or if she has had a serious allergic reaction to yeast or any other vaccine components (aluminium phosphate, sodium chloride, L-histidine, polysorbate and sodium borate)."
*exposure to borax may impair fertility or cause damage to an unborn child. (there were 5 reported cases of babies born with congenital birth defects to women who had the vaccine within 30 days of becoming pregnant.
*aluminium is implicated as a cause of brain damage, a suspected factor in Alzheimers Disease, dementia, seizures, comas, allergic skin reactions.
* polysorbate is known to cause cancer in animals.
Imunise Australia literature also states:
*Cervical cancer is not common in Australia
*Most women who have HPV, slowly clear the virus naturally and do NOT develop cervical cancer
*(HPV) is so common that four in five people will have had genital HPV infection at some time in their lives. Most genital infections with HPV do not cause any symptoms and people do not know they have the infection. (* girls will not be screened for any HPV infection prior to vaccination)
On the subject of safety, as usual the promotional brochure that states "This information is correct as at March 2007", (re-enforcing my belief that carrier pigeons are exceptionally slow between the US and AUS) makes no mention of the myriad of adverse events already being reported at an alarming rate after 6 months of vaccinating in the US.
See the NVIC website for the full story but - “Out of the 385 individual GARDASIL adverse event reports made to VAERS, (Vaccine Adverse Events Reporting Sysytem) two-thirds required additional medical care and about one-third of all reports were for children 16-years-old and under, with nearly 25 percent of those children having received simultaneously one or more of the 18 vaccines that Merck did not study in combination with GARDASIL. NVIC is calling on the FDA and CDC to warn parents and doctors that GARDASIL should not be combined with other vaccines and that young girls should be monitored for at least 24 hours for syncopal (collapse/fainting) episodes that can be accompanied by seizure activity, as well as symptoms of tingling, numbness and loss of sensation in the fingers and limbs, all of which should be reported to VAERS immediately.”
"There are twice as many children collapsing and four times as many children experiencing tingling, numbness and loss of sensation after getting a GARDASIL vaccination compared to those getting a Tdap (tetanus-diphtheria-acellular pertussis) vaccination. There have been reports of facial paralysis and Guillain-Barre Syndrome. And doctors who give GARDASIL in combination with other vaccines are basically conducting an experiment on their young patients because Merck has not published any safety data for simultaneous vaccination with any vaccine except hepatitis B vaccine."(Barbara Loe Fisher)
Also -
*Merck only studied GARDASIL in fewer than 1200 girls under age 16 in pre-licensure trials
*Merck has not published any safety data for simultaneous vaccination with any vaccine except hepatitis B vaccine
*There were several VAERS reports of HPV infection, genital warts and cervical lesions after GARDASIL vaccination. It is unknown if the girls were infected with HPV before being vaccinated or if GARDASIL failed to protect them. One case of HPV infection occurred in a 22-year-old girl who had participated in a Merck GARDASIL trial in 2003 when she had shown "strong conversion to all 4 vaccine types" but "tested positive for high risk HPV" in 2006, according to the VAERS report.
“There have been estimates that fewer than 10 percent, even as low as 1 to 4 percent, of adverse events which occur after prescription drug or vaccine use are ever reported to government adverse event reporting systems.”
"If only 1 to 4 percent of all adverse events associated with GARDASIL vaccination are being reported to VAERS, there could have been up to 38,000 health problems after GARDASIL vaccination in 2006 which were never reported," said Fisher. "How many girls are really having short-term health problems associated with getting this vaccine that could turn into long-term neurological or immune system disorders? And how many will go on to develop fertility problems, cancer or damage to their genes, all of which Merck admits in its product insert that it has not studied at all? We just don't know enough to be mandating GARDASIL for anyone, much less vulnerable 11 to 12 year old girls entering puberty."
http://www.nvic.org/
But wait! There's more!
"Diane M. Harper, a lead researcher in the development of the humanpapilloma virus vaccine, says giving the drug to 11-year-old girls "is a great big public health experiment." Not only that, she says it's not been tested for effectiveness in younger girls, and administering the vaccine to girls as young as 9 may not even protect them at all. And, in the worst-case scenario, instead of serving to reduce the numbers of cervical cancers within 25 years, such a vaccination crusade actually could cause the numbers to go up.
"It is silly to mandate vaccination of 11- to 12-year-old girls There also is not enough evidence gathered on side effects to know that safety is not an issue."
“HPV is not just spread through sex. We have multiple papers where that's documented. We know that 3-year-olds, 5-year-olds, 10-year-olds, and women who have never had sex have been found to be positive for the cancer-causing HPV types."
More Information by Patricia Bohackyi - PDF : Cervical Cancer Vaccine Deception
http://www.vaproject.org/
AND the vaccine costs 120.00 a shot and you have to get THREE and it is ONLY GOOD FOR FIVE YEARS meaning boosters would be needed.
Can everyone see that this is ONE BIG GOVERNMENT APPROVED possibly soon to be mandated experiment using our kids? I would never recommend it to anyone......male or female.......and some say boys would really need the shot too in order for this to be truly effective but MERCK does not yet know if the vaccine is effective in boys. They are currently doing their silly studies on that now. Personally I think everyone should steer clear of this....especially if someone tells you to give it to your little girl. AND by that I mean anyone under 13 years of age.....which is the next targeted range they are after. They want to immunize kids now with Gardasil as young as possible. I hate to think more kids would have to die or suffer long-term physical consequences because of playing around to see what will or won't happen with this vaccine. ALL the docs I work for are PUSHING this vaccine left and right to all their female patients and those patient's daughters! It has become a mandatory offering for them...and they push it big time. I know how the system works with drug companies and our docs.......and the government who "quietly" tells many what they have to do and not do. I KNOW this has been laid on the docs to PUSH this vaccine to all their patients and it happens over and over every day. AND IT DOES NOT PROTECT AGAINST ALL STRAINS OF HPV......only a couple......so the so-called 100% effectiveness of this vaccine in preventing cervical cancer is BULLSHIT!
Here's more:
There is a lot of discussion around the blogosphere right now about the HPV vaccine, because Texas has made it “compulsory.”
In fact, in most states, to include Texas, exemptions are available to parents for religious, philosophical, conscientiously held, or personal reasons. Here is exemption information from NVIC, the National Vaccine Information Center:
Legal Exemptions to Vaccination
Medical, philosophical or personal belief exemptions are worded differently in each state. To use an exemption for your child, you must know specifically what the law says in your state.
The following 18 states allow exemption to vaccination based on philosophical, personal or conscientiously held beliefs: Arizona, Arkansas, California, Colorado, Idaho, Louisiana, Maine, Michigan, Minnesota, New Mexico, North Dakota, Ohio, Oklahoma, Texas, Utah, Vermont, Washington and Wisconsin.
In many of these states, individuals must object to all vaccines, not just a particular vaccine in order to use the philosophical or personal belief exemption. Many state legislators are being urged by federal health officials and medical organizations to revoke this exemption to vaccination. If you are objecting to vaccination based on philosophical or personal conviction, keep an eye on your state legislature as public health officials may seek to amend state laws to eliminate this exemption.
All states allow a religious exemption to vaccination except Mississippi and West Virginia. …
Complete information here. In point of fact, all you have to do is assert a religious exemption in order to get it. Nobody has to vouch for you, sign for you, anything like that. Most parents don’t realize exemptions are available, that’s not information that is widely publicicized or that, for that matter is widely known, but exemptions are available in almost every state, and parents who choose not to immunize should take them. It’s a matter of simply filling out a line on the Immunization Record which states that parents have taken a philosophical/religious/personal/conscientious/medical exemption to immunization for their children. That’s all that’s required in most states.
The HPV vaccine is not safe, despite the claims of Merck:
The early reports of potential safety problems with GARDASIL raise concerns and questions that need to be addressed by government regulators, manufacturers and prescribing physicians. Specifically, the following concerns need to be addressed
Syncope, seizures and Guillian-Barre Syndrome have now been reported with hours to a week after GARDASIL vaccination. GARDASIL manufacturer, Merck, should add these serious adverse events to the product manufacturer insert.
Considering that over 20 girls have experienced syncopal episodes sometimes combined with seizures and serious injuries, physicians should consider only giving GARDASIL when the patient is safely laying down on the examining table. Because there seems to be syncopal reactions up until 15 minutes after vaccination, patients should be asked to lie down for 15 minutes after receipt of GARDASIL.
The information provided by Merck indicates that it is safe to administer GARDASIL with Hepatitis B vaccine. The prescribing information states, “Results for clinical studies indicate that GARDASIL may be administered concomitantly (at a separate injection site) with hepatitis B vaccine (recombinant). Co-administration of GARDASIL with other vaccines has not been studied.” [4] Due to the small number of girls aged 9 to 15 who appear to have been evaluated for GARDASIL safety in Merck clinical trials (fewer than 2,000) and lack of publicly available information about how many of these girls were given GARDASIL and hepatitis B vaccine simultaneously, the safety of administering GARDASIL and hepatitis B vaccine to all pre-adolescent girls is uncertain.[5]
Aside from Hepatitis B, Merck does not state that it is safe to simultaneously administer GARDASIL with any other vaccine. Considering that there are ongoing evaluations of a reported association between Menactra (meningococcal vaccine) and Guillain-Barre Syndrome, and Merck does not explicitly indicate that it is safe to administer to administer GARDASIL and Menactra simultaneously, consumers and clinicians should question whether administering both GARDASIL and Menactra at the same time is safe.
Similarly, adverse reactions were reported when GARDASIL was administered with eight other vaccines: Hepatitis A, MNQ (?), MEN (Menactra), TD (Tetanus and Diptheria Toxoids), DPP (Diptheria/Pertussis/Polio), PNC Prevnar (Heptavalent pneumococcal conjugate), DTaP (Diphtheria And Tetanus Toxoids and Acellular Pertussis Vaccine), and TDAP (Tetanus, Diptheria and Pertussis). Because Merck does not state that it is safe to administer simultaneously GARDASIL with any vaccine other than Hepatitis B, consumers and clinicians should question whether co-administration of GARDASIL and other vaccines is safe.
Most, if not all, of the reactions reported to VAERS were in response to the first of the three doses of GARDASIL. The Centers for Disease Control (CDC) Vaccine Information Sheet (VIS) developed for HPV vaccine states that severe reactions include “any unusual condition, such as a high fever or behavior changes. Signs of a serious allergic reaction can include difficulty breathing, hoarseness or wheezing, hives, paleness, weakness, a fast heart beat or dizziness.” [6] The CDC also states that “anyone who has ever had a life-threatening allergic reaction to yeast, to any other component of HPV vaccine, or to a previous dose of HPV vaccine should not get the vaccine.” Which of the reactions reported to VAERS constitute a “life-threatening allergic reaction” and which, if any, of the children and young adults who experienced reactions should receive additional doses of vaccine? At the October 2006 ACIP meeting, CDC staff stated that only “three serious reports were reported to VAERS after HPV vaccination in females 14 and 16 years of age. One of these patients had vasovagal syncope and was hospitalized overnight for observation.” [7]CDC’s summary of the first 76 VAERS reports suggests that CDC doesn’t regard the remaining reports as “serious.” CDC needs to clarify which of the reactions reported to VAERS constitute contraindications to further vaccination with GARDASIL and make this information available to the public and to prescribing physicians.
What were the short and longer-term outcomes for the individuals who experienced the reactions reported to VAERS? Is there information available that would help to predict the characteristics that predispose one to be at greatest risk of experiencing a serious reaction?
The CDC’s Vaccine Information Sheet indicates that allergy to yeast is a reason to avoid taking GARDASIL. Merck notes that contraindications to the vaccine include “hypersensitivity to the active substances or to any of the excipients of the vaccine. Individuals who develop symptoms indicative of hypersensitivity after receiving a dose of GARDASIL should not receive further doses of GARDASIL.” The prescribing information provided by Merck does not specifically note that yeast allergy is a contraindication to taking GARDASIL. Government regulators and the manufacturer need to address the discrepancy between these documents and clarify the issues related to yeast allergy and make this information readily available to the public and prescribing physicians.Additionally, Merck notes that vaccine ingredients include 225 mcg of aluminum (as amorphous aluminum hydroxyphosphate sulfate adjuvant), 0.78 mg of L-histidine, 50 mcg of polysorbate 80, and 35 mcg of sodium borate. These ingredients are not listed on the CDC’s VIS sheet. The public needs this information so that they can identify whether they have “hypersensitivities” to any of the ingredients and whether they are at risk of experiencing a serious allergic reaction. Hypersensitivities and known allergic reactions are critical pieces of information that need to be communicated to prescribing physicians in order to make the safest possible vaccination decisions…
Footnotes and entire article here
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