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The Bulletin: Gardasil Researcher Drops A Bombshell
Gardasil Researcher Drops A Bombshell
Harper: Controversal Drug Will Do Little To Reduce Cervical Cancer Rates
By Susan Brinkmann, For The Bulletin
Published:
Sunday, October 25, 2009
Dr. Diane Harper, lead researcher in the development of two human papilloma virus vaccines, Gardasil and Cervarix, said the controversial drugs will do little to reduce cervical cancer rates and, even though they’re being recommended for girls as young as nine, there have been no efficacy trials in children under the age of 15.
Dr. Harper, director of the Gynecologic Cancer Prevention Research Group at the University of Missouri, made these remarks during an address at the 4th International Public Conference on Vaccination which took place in Reston, Virginia on Oct. 2-4. Although her talk was intended to promote the vaccine, participants said they came away convinced the vaccine should not be received.
“I came away from the talk with the perception that the risk of adverse side effects is so much greater than the risk of cervical cancer, I couldn’t help but question why we need the vaccine at all,” said Joan Robinson, Assistant Editor at the Population Research Institute.
Dr. Harper began her remarks by explaining that 70 percent of all HPV infections resolve themselves without treatment within a year. Within two years, the number climbs to 90 percent. Of the remaining 10 percent of HPV infections, only half will develop into cervical cancer, which leaves little need for the vaccine.
She went on to surprise the audience by stating that the incidence of cervical cancer in the U.S. is already so low that “even if we get the vaccine and continue PAP screening, we will not lower the rate of cervical cancer in the US.”
There will be no decrease in cervical cancer until at least 70 percent of the population is vaccinated, and even then, the decrease will be minimal.
Apparently, conventional treatment and preventative measures are already cutting the cervical cancer rate by four percent a year. At this rate, in 60 years, there will be a 91.4 percent decline just with current treatment. Even if 70 percent of women get the shot and required boosters over the same time period, which is highly unlikely, Harper says Gardasil still could not claim to do as much as traditional care is already doing.
Dr. Harper, who also serves as a consultant to the World Health Organization, further undercut the case for mass vaccination by saying that “four out of five women with cervical cancer are in developing countries.”
Ms. Robinson said she could not help but wonder, “If this is the case, then why vaccinate at all? But from the murmurs of the doctors in the audience, it was apparent that the same thought was occurring to them.”
However, at this point, Dr. Harper dropped an even bigger bombshell on the audience when she announced that, “There have been no efficacy trials in girls under 15 years.”
Merck, the manufacturer of Gardasil, studied only a small group of girls under 16 who had been vaccinated, but did not follow them long enough to conclude sufficient presence of effective HPV antibodies.
This is not the first time Dr. Harper revealed the fact that Merck never tested Gardasil for safety in young girls. During a 2007 interview with KPC News.com, she said giving the vaccine to girls as young as 11 years-old “is a great big public health experiment.”
At the time, which was at the height of Merck’s controversial drive to have the vaccine mandated in schools, Dr. Harper remained steadfastly opposed to the idea and said she had been trying for months to convince major television and print media about her concerns, “but no one will print it.”
“It is silly to mandate vaccination of 11 to 12 year old girls,” she said at the time. “There also is not enough evidence gathered on side effects to know that safety is not an issue.”
When asked why she was speaking out, she said: “I want to be able to sleep with myself when I go to bed at night.”
Since the drug’s introduction in 2006, the public has been learning many of these facts the hard way. To date, 15,037 girls have officially reported adverse side effects from Gardasil to the Vaccine Adverse Event Reporting System (VAERS). These adverse reactions include Guilliane Barre, lupus, seizures, paralysis, blood clots, brain inflammation and many others. The CDC acknowledges that there have been 44 reported deaths.
Dr. Harper also participated in the research on Glaxo-Smith-Kline’s version of the drug, Cervarix, currently in use in the UK but not yet approved here. Since the government began administering the vaccine to school-aged girls last year, more than 2,000 patients reported some kind of adverse reaction including nausea, dizziness, blurred vision, convulsions, seizures and hyperventilation. Several reported multiple reactions, with 4,602 suspected side-effects recorded in total. The most tragic case involved a 14 year-old girl who dropped dead in the corridor of her school an hour after receiving the vaccination.
The outspoken researcher also weighed in last month on a report published in the Journal of the American Medical Association that raised questions about the safety of the vaccine, saying bluntly: “The rate of serious adverse events is greater than the incidence rate of cervical cancer.”
Ms. Robinson said she respects Dr. Harper’s candor. “I think she’s a scientist, a researcher, and she’s genuine enough a scientist to be open about the risks. I respect that in her.”
However, she failed to make the case for Gardasil. “For me, it was hard to resist the conclusion that Gardasil does almost nothing for the health of American women.”
Germans Unhappy with Alternative Swine Flu Vaccine for Politicians
You Tube Video: Germany begins controversial swine flu vaccination
Spiegel: Germans Unhappy with Alternative Swine Flu Vaccine for Politicians
“Damage control is the name of the game in Berlin on Monday as politicians rush to deny that they are receiving a better, safer swine flu vaccine than ordinary Germans. The first of 50 million doses arrived in Germany on Monday.
One might think that the arrival in Germany of the first of 50 million doses of swine flu vaccine on Monday might be cause for celebration. But with news breaking over the weekend that top government officials in Berlin will be injected with an alternative vaccine — one widely seen as safer — a debate about an alleged two-class medical system has erupted.
SPIEGEL over the weekend reported that Chancellor Angela Merkel, a number of her ministers and other government officials would receive a vaccine manufactured by the pharmaceutical company Baxter — the same vaccine that the German military opted for, as was reported last week.
The mass-circulation tabloid Bild on Monday plastered the story on its front page on Monday, assuring its readers that “experts are accusing the government” of serving up “second class medicine” to ordinary Germans.
Fevers and Headaches
The controversy centers on an additive included in the vaccine manufactured by pharmaceutical giant GlaxoSmithKline. The additive includes an inactive strain of the entire flu virus as opposed to virus fragments. Critics say the additive can increase the risk of side effects from the flu vaccine such as fevers and headaches.
Supporters counter that the additive is safe, and its use allows the drug manufacturer to quickly produce more doses of the vaccine. The SPIEGEL story mentioned that the GlaxoSmithKline vaccine, with the additive, has undergone more testing than the Baxter version.
An Interior Ministry spokesman told SPIEGEL that the Baxter vaccine had been ordered for all ministries and other agencies as well as for the employees of the Paul Ehrlich Institute, the authority responsible for approving vaccines.
Merkel’s spokesman Ulrich Wilhelm on Monday denied that Merkel was taking a different vaccine than the one available to ordinary Germans. He said that the Baxter vaccine had been ordered four months ago as part of a deal hammered out one year ago and has nothing to do with recent concerns surrounding the GlaxoSmithKline vaccine.”
…The weekend scandal has drowned out a second debate which has been raging in recent weeks in the US and which has also found resonance here in Germany: whether such a massive vaccination program is necessary in the first place.
Wolf-Dieter Ludwig, chairman of the Drug Commission of the German Medical Association, has called the planned vaccination campaign a “scandal.” “The health authorities have fallen for a campaign from the pharmaceutical companies, who simply want to earn money with an alleged threat,” he told SPIEGEL.’
TIME Magazine: In Germany, a Better Vaccine for Politicians?
“Critics are calling it a two-tier health system — one for the politically well connected, another for the hoi polloi. As Germany launched its mass-vaccination program against the H1N1 flu virus on Monday, the government found itself fending off accusations of favoritism because it was offering one vaccine believed to have fewer side effects to civil servants, politicians and soldiers, and another, potentially riskier vaccine to everyone else. The government had hoped that Germans would rush to health clinics to receive vaccinations against the rapidly spreading disease, but now rising anger over the different drugs may cause many people to shy away.
Amid growing fears of a possible global flu pandemic, the German government prepared for its mass-vaccination campaign earlier this year by ordering 50 million doses of the Pandemrix vaccine, enough for a double dose for 25 million people, about a third of the population. The vaccine, manufactured by GlaxoSmithKline, contains an immunity-enhancing chemical compound, known as an adjuvant, whose side effects are not yet entirely known. Then, after a report was leaked to the German media last week, the Interior Ministry confirmed that it had ordered a different vaccine, Celvapan, for government officials and the military. Celvapan, which is made by U.S. pharmaceutical giant Baxter, does not contain an adjuvant and is believed to have fewer side effects than Pandemrix. (See how not to get the H1N1 flu.)
Note from Jenny: The side effects from the adjuvent Squalene have been completely researched, studied, and reported for sixty years. Massive amounts of death, disability, and auto immune dysfunction are going to be the side effects from taking this vaccine. Squalene toxicity is DEFINED by a purplish hue to the skin on cheeks and the chest just before death. Watch for it. When people start to die with that purple rash on their skin, you will know they have died from Squalene poisoning. I am anticipating the health authorities saying that the virus has “mutated” when this happens and then declaring that everyone has to get the shot.
Anger at the news was widespread in Germany. “If mass vaccination is considered to be necessary, then everyone should be treated the same way,” says Birgitt Bender, health spokeswoman for the Green Party. Ulrike Mascher, head of the VdK social-welfare association, says giving government officials a vaccine that’s different from that given to the rest of the population sent the “wrong signal” and gives many people “the impression that they are second-class patients.” A story on the front page of the mass-circulation Bild newspaper accused the government of giving “second-class medicine” to regular Germans.
Doctors and medical experts are divided over the safety of Pandemrix. While some say it’s the best vaccine available, others have serious misgivings about it. “The Pandemrix vaccine can’t be recommended for pregnant women or young children because it has an increased risk of side effects. Pandemrix has an adjuvant which hasn’t been tested sufficiently up until now,” Alexander Kekulé, a virologist at the University of Halle, tells TIME. “Celvapan is a whole-virus vaccine, which has fewer side effects than Pandemrix, but it leads more often to fever or local swelling when compared with the normal seasonal-flu vaccine,” he adds. Although Kekulé calls the government’s handling of the vaccination program a “scandal,” he says government officials and soldiers are not necessarily getting a better deal with Celvapan. “Neither Celvapan nor Pandemrix are ideal,” he says. (See what you need to know about the H1N1 vaccine.)
The Interior Ministry hit back at suggestions of preferential treatment, saying it had ordered about 200,000 doses of the Celvapan vaccine from Baxter before the differences between the two vaccines were documented, and the government was bound by the terms of its contract. The government also points out that both Pandemrix and Celvapan have been approved by the European Union and that other countries, such as Britain and Sweden, are using the Pandemrix vaccine. In an attempt to put a lid on the simmering controversy, Chancellor Angela Merkel’s spokesman, Ulrich Wilhelm, said the German leader would consult with her doctor in the next few days, and if she decided to receive a jab, it would be Pandemrix. (See pictures of thermal scanners hunting for swine flu.)
At least 26,000 people have been infected with swine flu in Germany, resulting in three deaths. Although the majority of patients have experienced only mild flulike symptoms, a steady increase in the number of cases of H1N1 in recent months has raised alarm across the nation. In its latest report, the Robert Koch Institute, the federal agency for infectious diseases, said new cases in Germany have jumped to about 1,600 each week, double the 700 to 800 weekly cases reported in early autumn. With the onset of winter, when seasonal-flu infections typically peak, many experts are concerned that H1N1 infections will spike dramatically. Klaus Osterrieder, a virologist at the Free University of Berlin, now fears that with the worries over the possible risks associated with Pandemrix, many people will avoid getting a vaccine altogether. According to a survey conducted on Oct. 23 by the Emnid Institute, only 13% of Germans said they wanted to receive a swine-flu vaccine this winter. (Read “Child-Care Centers and Parents Brace for Flu Season.”)
“The public debate is bad because it raises questions about the whole vaccination program,” Osterrieder says. If the government doesn’t find some way to remedy the current public relations disaster and clear up the confusion over the different swine-flu vaccines, it could be faced with an even greater emergency, especially if the country’s hospital wards start overflowing with flu patients in the coming months.”
National emergency declaration in USA allows use of squalene
The decision by President Barack Obama to declare a National Emergency over the swine flu pandemic will allow vaccines and drugs such as the adjuvant squalene which have not been approved by the FDA to be used by doctors, hospitals and vaccine clinics.
There is a large body of scientific evidence that shows that squalene in the anthrax vaccine was responsible for causing the Gulf War Syndrome and other diseases in US and UK soldiers.
The swine flu jab vaccine contains up to a million times more squalene than the anthrax vaccines, which afflicted an estimated 25 % of all soldiers who got the jab.
Squalene is illegal in the USA and UK, but emergency regulations allow the government to use drugs that have not been proven for safety.”
Jenny Hatch with Andrew in 1996 – ready for church on his blessing day
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Deadly Vaccines: Swine-flu emergency! What does that mean?
WND: Swine-flu emergency! What does that mean?
Is president’s proclamation formality, or institution of Obama martial law?
“President Obama announced today that he has declared a “national emergency” over the H1N1 virus, a phrase with an ominous sound, but with little explanation offered by most of the news media.”
Jenny Hatch

The Natural Family BLOG
Healthy Families Make A Healthy World!

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Arkansas DHS vaccinates 36 children with swine flu vaccine against parents objections
In a radio interview with Greg Szymanski on September 30, Cheryl Barnes founder of CPS Legal Watch, revealed that the State of Arkansas has given 36 children the swine flu vaccine against their parents’ wishes. The 36 children were taken into custody last fall by the Department of Human Services because the state said they were in jeopardy due to their parents’ involvement with the Tony Alamo Ministries Church.
The State of Arkansas does require that children get immunized if they are attending school. However, Arkansas does allow for religious and medical exemptions. The parents of the 36 children did not want their children vaccinated because it is against their religious beliefs. According to Barnes, all 36 children have received at least one of the three series of H1N1 flu shots and some have received all three.
The swine flu vaccine has come under fire from a number of people from a variety of backgrounds and beliefs who have alleged that it is not safe. Health care workers in New York State have been ordered by the New York State Department of Health to get immunized against the swine flu. Some health care workers have been fired for refusing to get immunized and health care workers have held protests in Albany.
Barnes also stated that the 36 children in Arkansas have been vaccinated against other illnesses against their parents’ religious beliefs, including the vaccination of all of the girls with Gardasil. Attorneys for CPS Legal Watch filed a motion to stop the vaccinations of these children, but the judge sat on it for six weeks, after which in many cases it was moot, because the children had already been vaccinated and because Judge Griffin of Miller County had terminated the parental rights of some of the parents.
Even though all states allow for medical exemptions for vaccinations and all but two states allow for religious exemptions, parents have been charged with medical neglect for not immunizing their children according to http://mothering.com/cps
Jenny Hatch

The Natural Family BLOG
Healthy Families Make A Healthy World!

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