Multigenerational Vaccine Indoctrination

By Author, Dr. Sherri Tenpenny, Undue Influence, Vaccine Propaganda

Multigenerational Vaccine Indoctrination

No Comments 14 February 2010

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Posted on Dr. Sherri Tenpenny’s Facebook Page

I have frequently spoken about the multigenerational indoctrination about the belief in vaccines. Where did that come from? We need to unwind it.

The book, State of Immunity, by James Colgrove, is absolutely amazing and lays out in detail how the government, public health officials and life insurance companies coerced us into believing in the importance of vaccination.

We don’t study history anymore, which is a very sad state for our Country. If we did, we would see the patterns, and hopefully choose differently. Here’s a snip from Colgrove’s book (pg 92) about the 1920s diphtheria campaigns. The intensiveness of the process — and their success — have been repeated over and over, starting with polio and going through Swine flu.

We can’t fight them financially; they own all the money and have all the power. Now that we have seen the PlayBook, we need a different strategy. We have to be smarter…and get everyone to understand how the Game is Played.

Dr Sherri
PS. If you are interested in this topic, this book is a MUST for your personal library!
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In the nineteenth century, fear was proven to be a powerful motivation prompting people to seek vaccination. But the risk of diphtheria was much less than the disfiguring risk of smallpox. ….To get people to accept vaccination, the threat of diphtheria would have to be magnified and dramatized….

Campaigns were launched in 1926 across upstate New York and continued over three year. Families were reached by dozens of public health nurses that went door to door, canvassing patients and urging them to be vaccinated. Special immunization clinics offering fre or low-cost injections were set up in schools, dispensaries and other locations. Campaigns involved civic organizations and local businesses. Organizations such as the Lions Club donated lollipops to children following their shots.

Virtually every state newspaper ran advertisements, articles and editorial commentary. Radio broadcasts carried the message into homes. Billboards, posters, and placards were ubiquitous. Local schools held competitions between classes to achieve the highest rates of vaccination; students entered contests for the best essay and porter demonstrating the importance of diphtheria protection. Young people were awarded gold stars and badges after receiving their injections.

Parades, pageants and publicity stunts were staged. The mayor of Yonkers posed for news cameras as his three children receive their shots; in Yonkers and Mount Vernon, an army airplane scattered handbills urging immunizations. The Boy Scouts on the roofs of buildings wagging anti-diphtheria messages to kick off campaigns. ….Every effort included happy mothers pushing baby carriages down the street after being vaccinated.

The scope of the 1929 anti-diphtheria drive was remarkable. The health department sent almost 250,000 letters to mothers. The Catholic dioceses of Manhattan and Brooklyn sent letters to all parishioners and the principals of parochial schools and made announcements a t masses. Leaflets were included in the city’s electric and gas bills. Public schools distributed one million fliers to students.

Times Square had two rotating billboards and painted signs more than two hundred feet long were the largest pieces of outdoor advertising ever seen in the city. Some three hundred radio talks were broadcast. A series of four short films was shown in five HUNGDRED movie theaters. Virtually every newspaper in the city, including the large dailies, the foreign language press, local borough and neighborhood papers and trade journals, carried articles about the importance of immunizations. Subways, elevated trains, streetcars, and busses displayed placards. The city’s largest department stores donated advertising space in newspapers. Posters were displayed in chain stores. Posters, brochures and leaflets were translated into the ten most widely spoken foreign languages. Six ‘health mobiles” (which were snow removal trucks converted into traveling clinics), toured neighborhoods, parks and beaches.

The net effect was a change in professional ideology. The new perspective located the source of disease within the individual, rather than the environment, and saw persuasion rather than compulsion as the most appropriate and powerful tool for the implementation of mass vaccination.

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Health Doesn’t Come Through a Needle

Autism, Dr. Sherri Tenpenny

Health Doesn’t Come Through a Needle

No Comments 08 February 2010

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Dr. Sherri Tenpenny
DrTenpenny.com
02/08/2010

From Maine to Maui, Vancouver to Miami, autism rates across North America are soaring. As of February, 2010, there are an estimated 300,000 severely autistic children in this country — requiring nearly $9billion per year in services. Then numbers in Canada are equally staggering. Considering the country’s much smaller population, autism affects an estimated 190,000 children in Canada. And these numbers don’t reflect the millions of children “on the spectrum” in both countries.

Parents include OT, PT and speech therapy into their routine, approaching these activities as though they are a normal part of childhood, like soccer and piano lessons. Doctors have started to say, “Well, two years is when kids get asthma”, as though becoming asthmatic is a growth milestone.

There is one unifying factor affecting children, from sea to shining sea. It’s not genetics; genetics between families are different. It’s not environmental exposures; some kids live in the Projects, some live in Gated Communities. It’s not food; some kids eat only organic, some eat mostly McDonalds. It’s not exercise; some kids are athletes; others are couch potatoes.

What touches almost all children and is the most likely ‘smoking gun’ for the epidemic of chronic illness and autism across North America (and beyond), are childhood vaccinations.

Read the rest of the article here.

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Dr. Sherri Tenpenny, News

Defending The Right to Poison

1 Comment 07 November 2009

Dr. Sherri Tenpenny
The National Expositor
04 November, 2009 09:47:00

Until my dying breath I will never understand how adamantly people defend their right to inject themselves and their children with poisons — viruses and chemicals called “vaccines” — under the ruse that this slurry is harmless and will somehow keep them healthy.

Dr. Tenpenny – It continually breaks my heart that people have to take a bullet to the head before they find out bullets can be deadly… and they wish they had listened when they were warned not to play with loaded guns.

I have a little person in my office who had 10 rounds of antibiotics and 17 vaccines by 20 months of age. Yes, now autistic. That should be assault with deadly weapons and the doctor should be in jail. Instead, the parents were kicked out of their pediatrician’s practice for refusing more vaccines and wanting to get their child well. With these annoying, non-compliant parents out of the way, that doctor can continue to do what vaccinators do: Inject toxic substances into children, ruining their health and the lives of the child’s family members.

Parents have had years to get informed; my books and DVDs have been available for years since 2002. Dozens of others have been trying to educate people for as long — or longer – than I have. Parents of vaccine-injured children have implored fellow parents to question vaccines and demand answers. More recently, very visible persons – Jenny McCarthy and Dierdre Imus – have warned about vaccines, begging and pleading with parents to stop — JUST STOP.

I get emails almost every day that say things like, “I got your DVD and your book…but I have a question: should I get a flu shot?” WHAT?@!>! My mouth drops to the desk and I have to find a way to nicely but firmly say, “No, you should not get the flu shot.”

That may seem harsh and pretty bold, but we are coming in to some very turbulent times. Soft language and hand holding is no longer in order. The stranglehold of fear, perpetrated by those in white coats and the medical bureaucrats in Washington DC who take their marching orders from pharma, continues. Funny how they can be the “experts” when it is obvious they don’t even understand – and probably don’t even read – their own medical literature.

Being in the business of waking people up to the hazards of vaccines certainly has its ups and downs, as many of you know. Today’s news was particularly discouraging. The woman bragging that she stood in line for FIVE hours to get an H1N1 shot. Schools vaccinating children without parental consent. Several more miscarriages reported after H1N1 vaccination. The strange outbreak in the Ukraine that the WHO has already declared to be an outbreak of “novel H1N1” — how can that be? And this proclamation will be used to REALLY terrify people into getting vaccinated.

Until my dying breath I will never understand how adamantly people defend their right to inject themselves and their children with poisons — viruses and chemicals called “vaccines” — under the ruse that this slurry is harmless and will somehow keep them healthy.

The only thing to do, really, is just keep putting one foot in front of the next, being grateful for those who are waking up and supporting them. The rest, well, they may sadly have to find out what it feels like to get hit by that stray bullet.

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Dr. Sherri Tenpenny, H1N1, News

Dr. Tenpenny: Whose Decision Is It, Anyway?

No Comments 27 October 2009

Dr. Sherri Tenpenny
Huffington Post
October 27th, 2009

There has been much discussion about using schools for an “all out” vaccination campaign this fall, for both the regular flu shot and the new H1N1 vaccine.1 According to authorities, students would ideally be vaccinated before school starts, but the swine flu vaccine won’t be available until mid-October, making schools a logical place to begin mass vaccination.

According to permission slips issued in some school districts in Maine, parents must be present when their child is vaccinated if the child is in grade K through 2. For older students, parents are not required to attend, but they may do so if they wish. In the fine print of the permission slips, parents are notified of the date that a second, seasonal influenza vaccine will be administered to children who have never received a regular seasonal flu shot before.2 While the Maine Department of Education is quick to point that this is not a mandatory program, if the government declares an Influenza Pandemic Emergency, will those who question the safety and efficacy of both the season flu shot and the new swine flu shot retain their right to refuse for their kids?

Parental Consent vs. Physicians and the State

Parents have fewer rights over the health and welfare of their children that they may recognize. This concept reaches back into antiquity when the rulers in Sparta forcibly removed children from families so they could be indoctrinated with the willingness and importance of dying for the State in war. 3 This was also the model for Plato’s idealized Republic. Interestingly, in 1918, the congress of the Communist Party’s education workers in Russia asserted, “We must remove the children from the crude influence of their families.” 4

When it comes to medical decisions, physicians are charged with ensuring the medical standard of care, defined as a treatment process that a clinician should follow for a given circumstance, is carried out on children, even over the objections of their parents. Doctors not only have the right to step in. All states have laws making it mandatory to report perceived medical abuse and neglect to Children’s Protective Services (CPS). Physicians usually make the call when s/he feels the action–or inaction–of a parent places the child in danger of death or disability. A common example is a forced transfusion of blood to save the life of a child whose parents are Jehovah’s Witnesses. However, not vaccinating has come under scrutiny and in some circles is starting to be viewed as medical neglect. The American Academy of Pediatrics recently concluded that, “Continued (vaccine) refusal after adequate discussion should be respected unless the child is put at significant risk of serious harm (as, for example, might be the case during an epidemic). Only then should state agencies be involved to override parental discretion on the basis of medical neglect”.5

Wide support and extensive court precedence exists to back a doctor’s discretion to call in CPS. The rationale for this authority was clearly written in a 1996 paper that states, “Whether (the guardians) are sincere, sane, and in every other capacity model parents, their insistence upon treatment that is scientifically inferior to conventionally accepted treatment is abusive, even if their intent is not.”6 The current system, in its original intent, was set up to protect obviously abused and neglected children. The system would be a good one if medical professionals were amenable to common sense.

Unfortunately, common sense isn’t very common these days and disagreeing with your doctor can lead to serious consequences. Because the government agrees with the premise, “Doctor Knows Best,” parents can be deemed unfit when they refuse a medical treatment. Children can be removed from the home by CPS until proof of parental fitness is determined by a judge. The judge can also be the doctor himself: Physicians have the right to eject entire families from their practice when an obstreperous patient refuses – or even questions – routine vaccinations.

There have been several high-profile standoffs in the last several years where judges, medical doctors and the State have forced medical treatments on children against the objections of their parents.

In January, 2005, 13-year-old Katie Wernecke was diagnosed with Hodgkin’s disease. When Katie’s parents, Michele and Edward Wernecke, refused radiation treatments for their daughter, Texas CPS intervened. Katie was placed in foster care for four months and her mother was arrested on charges of interfering with child custody.

In July, 2006, the story of 9-month-old Riley Rogers made the news when he was diagnosed with a kidney problem that required emergency surgery. His mother disagreed and smuggled her son out of the hospital. Several days later, he was found and sent back to the hospital; the mother was charged with second-degree kidnapping and sent to jail. As it turned out, the surgery was not emergently needed after all.

Also in 2006, the story of Abraham Cherrix resulted in a change in the law in Virginia. After enduring three months of ineffective treatments for Hodgkin’s lymphoma, Abraham rejected his doctor’s recommendation for a second round of chemotherapy. He chose to use more natural, nontoxic methods that included alternative medicine. A judge ordered him back to chemotherapy, starting a debate on whether the government should get involved in family medical decisions. A compromise was reached in Accomack County Circuit Court: Abraham was not required to have chemotherapy if his family consented to treatment with a radiation oncologist who used both conventional and alternative methods. As a result of this high-profile case, Gov. Timothy M. Kaine signed a bill dubbed “Abraham’s Law,” giving parents and children more leeway in refusing medical treatment. 9

These stories should raise the eyebrows of every parent, leading them to ask the question, “Who really owns your child?” and more to the point, “Who owns your child’s body?” At what age a child “officially” become the age of majority in the U.S and have the right to decide what goes in his body?

Children Making Adult Decisions

The answer varies widely among the states and in some locales, the very young have the right to make very big decisions. For example, a youth can legally get married with parental consent in Georgia, Mississippi, Michigan, and North Carolina when 15 years of age. In Texas, 14-year-olds can wed with judicial consent, and amazingly, New Hampshire and Pennsylvania will even allow 13-year-old girls to marry with parental consent and court permission.

However, most states seem to delineate 16 years of age as the transition to adulthood. Nearly every state will allow 16 year old to marry with parental consent. At 16, a teen can hold a full-time job, travel alone outside the country, hold a driver’s permit, and have full responsibility for someone’s children as a baby sitter. In many states, 16-year-old can even be tried as an adult for murder.

When it comes to consent to medical care, the focal point of the debate over a minors’ access to confidential services and the right to determine his or her own care originated in 1970 with the passage of the Title X family planning program. Since its inception, services supported by Title X have been available to anyone who needs them without regard to age.

With the passage of time, the ability for minors to legally and fully consent to a range of sensitive health care services–including sexual and reproductive health care, mental health services and alcohol and drug abuse treatment–has expanded dramatically. The trend was based on the presumption that while parental involvement in minors’ health care decisions is desirable, many minors will not participate in medical services if forced to involve their parents. In most cases, state consent laws apply to all minors age 12 and older. These examples are eye-popping:

In 25 states and the District of Columbia, all minors (12 and older) can receive contraceptive services without parental participation.

In 28 states and the District of Columbia, all minor parents have the right to place their child for adoption. Of these, only 4 states (LA, MI, MN, RI) require parental consent.
In three states (CT, ME, MD) and the District of Columbia explicitly allow minors, 12 years of age and older, to consent to an abortion without involvement or notification of a parent. Only 22 states require parental consent and only 11 require a parent to be notified prior to an abortion.12

Of the 35 states with specific statutes, 30 states allow a minor to obtain authorization for an abortion from a judge without informing her parents. This option, given to protect a minor’s constitutional right to privacy, has been upheld by the U.S. Supreme Court.13

All this latitude has been given to minors to ensure they have rights for consenting to treatment. But- and this is key – they have little or no rights when it comes to refusing medical treatment forced upon them by doctors and the government, even when their parents support their right to refuse.
So, where is the line between the right to refuse a medication or a vaccine and the right of the state to forcibly intervene, even in the event of a declared national emergency? Who gets to make the decision? Will it be parents and smart teens, or persons in white lab coats and black robes? For me, I will fight to maintain the line between me and “them” at the level of my skin.

Notes:

1 “Vaccination Program That Targets Children First May Lessen Spread of Swine Flu This Fall,” WebMD News. September 10, 2009

2 “Schools in Maine Participating With Flu Vaccinations.”

3 “The Free Market and Education: A Review,” by Ken Schoolland. 1996.

4 Ibid. Ken Schoolland. www.fff.org/aboutus/press/schooland.asp

5 Salmon DA, Omer SB. “Individual freedoms versus collective responsibility: immunization decision-making in the face of occasionally competing values.”

6 Rosen, J Emergency Med. 1996;14:241-243.

7 “State-sponsored medical terrorism: Texas authorities arrest parents, kidnap their teenage daughter, and force her through chemotherapy against her will”

8 “Baby undergoes surgery despite mom’s worries.” by M. Alexander Otto. The News Tribune. July 2nd, 2006.

9 “Assembly Gives 14-Year-Olds A Say on Key Medical Care,” Washington Post. February 24, 2007.

10 Wikipedia: Marriageable age

11 Minors and the Right to Consent to Health Care The Guttmacher Report on Public Policy. August, 2009.

12 An Overview of Minors’ Consent Laws

13 Ibid. Minors’ Consent Laws.

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By Author, Dr. Sherri Tenpenny

Flu Vaccines and the Risk of Cancer

No Comments 15 September 2009

Flu Vaccines and the Risk of Cancer

Sherri Tenpenny, DO September 4, 2009

Much concern has been generated over the upcoming new swine flu H1N1 vaccines that are being rushed to market. Clinical trials will be short – less than three weeks – and the potential for the addition of toxic oil-in-water adjuvants to be added at the last minute to stretch the vaccine supply is disconcerting. However, the problems with flu shots go beyond current concerns. The new manufacturing process for flu shots, called cell-line technologies, are little understood and have the potential for serious, long term consequences.

Manufacturing the “regular,” annual flu shot

Each year, between January and March, an FDA advisory panel selects the three influenza strains expected to be in circulation during the upcoming flu season. Admitting that the process is an “educated guess,” the CDC sends the selected seed virus to the FDA for approval prior. Seed virus is then distributed to manufacturers for production.

The annual flu shot contains three viral strains: two type influenza A viruses and one type influenza B. Most commonly, two of the viruses are the same viruses included in the preceding year’s shot. The third virus is typically a new strain in circulation. This is the purported reason for giving the shot each year. The new strain is modified through a laboratory process called reassortment to ensure that it can readily grow in eggs. Once the modification is complete, all three viruses proceed through tricky manufacturing steps to create what goes in that vial.

The cumbersome flu shot production process utilizes up to 500,000 fertilized chicken eggs per day for up to eight months. Hundreds of millions of fertilized eggs become “mini-incubators” for cultured viruses. When the chick embryos are 11-days old, the amniotic membrane (the egg white) is manually injected with a drop of viral-containing solution. Several days later, the gooey viral suspension is centrifuged to remove as much chicken blood and tissue from the solution as possible. Residual egg protein remains within the final vaccine solution and is the reason why persons with an egg allergy are advised against receiving the flu shot.

The entire process, from viral selection to viral harvest, can take up to nine months.[i]  With the potential for a pandemic and the Director General of the WHO, Margaret Chan, requesting up to 4.9 billion of flu shots to vaccinate the world[ii], the slow lead time and labor-intensive production process cannot meet the demand for massive quantities of pandemic flu vaccine.

Enter Cell Line Technology

Cell line technologies, the use of cells and tissues for growing viruses found in vaccines, have been used since the 1950s. Examples include calf lymph for smallpox vaccines; African green monkey cells (AGMK cells) for polio vaccines and mouse brain cells for the Japanese encephalitis vaccine. In the 1960s, cells from aborted human fetal tissue, called MRC-5 and WI-38 cells, were developed and are still used for the manufacture of rubella chickenpox, hepatitis A and shingles vaccines.

Since the early 2000s, dozens of human and animal tissues have been investigated for use in viral vaccines, especially for the production of influenza shots. Batches of vaccine can be produced in less than six weeks instead of just one crop per year with eggs, a particularly useful methodology for ramping up production of flu shots.While many of the new cell lines are still considered experimental, cell line techniques have attracted all the major players in the vaccine and biotech industry.

Prior to 2007, cell lines were little used for flu shots, primarily for logistical reasons: Flu shots made from cells instead of eggs required a complete retooling of existing production facilities. None of the manufacturers were willing to invest the hundreds of millions of dollars and the five to seven years to construct new vaccine plants. But when the threat of the bird flu pandemic was hyped in 2006, the government opened is coffers and spilled billions of dollars into the pockets of the drug companies, giving them the capital to build new flu shot production facilities. By 2012, the first cell line factory will be completed in North Carolina. Vaccine giant, Novartis, will then have the capacity to produce 150 million flu shots per year, making it the number one commercial production plant for influenza vaccines and the adjuvant MF-59, in the world.

Cell Cultures: The Next Frontier in Vaccine Production

Several cell lines are currently under investigation. Novartis’ EU-approved flu shot, Optaflu, was produced using a cell line called Madin-Darby (MDCK), cells extracted from the kidneys of a female cocker spaniel. Dutch giant, Solvay Pharmaceuticals, has been working with MDCK cells since the early 1990s.

Another independent company, Protein Sciences Corporation, has been working on a patented influenza vaccine produced from caterpillar eggs. This vaccine strategy, known commercially as FluBlok, isolates a purified concentration of (H) antigen on the surface of an influenza virus and inserts the antigen into a second virus called a baculovirus. The (H)-containing baculovirus is then inserted into insect cells growing in culture. Several clinical trials involving the bug-created vaccine have shown that the antigens elicit a strong antibody response in humans.[iii] The vaccine, no doubt, contains snips of insect DNA. This technology is being tested in Europe and is not yet approved for use in the US.

A third type of cell line, called PER.C6 cells, is derived from retinal cells of aborted fetal tissues. The fetal cells are transformed by infecting them with an adenovirus, turning them into “immortalized” cells and the capability to replicate endlessly. By their very nature, these cells are neoplastic (cancer-causing); researchers refer to them as “oncogenic” cells. If tumors are formed when the cells are injected into experimental animals, the cell lines are beyond oncogenic; they are tumorigenic.

A serious concern about whole, live PER.C6 cells is that they are capable of causing tumors when transplanted into the skin of mice. The FDA requires a filtration method to be used during vaccine production that is designed to removes all cells before the final product is packaged. Even though several studies have been conducted to assure vaccine developers that PER.C6 cells do not cause cancer and do not contain stray tumor causing viruses,[iv] the risk of the cells making their way into the final vaccine products remain.

The risks of residual retinal DNA and stray viral contaminants from the animal tissues getting into flu shots are real. DNA snips are classified as either “infectious” or “oncogenic” by researchers who worry that the stray DNA is being incorporated into the recipient’s DNA, even thought FDA regulations insist on the “importance of minimizing the risk of oncogenesis in vaccine recipients.” Manufacturers have been instructed to ensure the final vaccine contains less than 1 million residual animal cells and the amount of stray DNA is less than 10 ng. per vaccine.[v] These regulations admit that animal DNA is injected into human babies and adults with every shot.

Is every lot tested for purity and these parameters?  No. Spot-checked lots are sent to the FDA and the FDA trusts the word of vaccine manufacturers that these standards have been met.

Tumorigenic Cells: The Risks Are Known

Since 1998, the FDA and its subdivision, the Centers for Biological Evaluation and Research (CBER), have been drafting regulations to allow use of both oncogenic and tumorigenic cell lines to be used in vaccine production. The FDA is fully aware that the new cell lines, especially the PER.C6 cells, have substantial risks, including the risk of potentially deadly adventitious [stray, outside] viruses making their way into shots. For example, the FDA acknowledges that the SV 40 virus (simian virus 40 from monkey kidney cells) was in the early polio vaccines and acknowledges the risks:

“The experience in the early 1960s with SV40 contamination of poliovirus and adenovirus vaccines and the continuing questions regarding whether SV40 could be responsible for some human neoplasms [cancers] underscores the importance of keeping viral vaccines free of adventitious agents [viral contaminants].

This is particularly important when there is a theoretical potential for contamination of a vaccine with viruses that might be associated with neoplasia [cancer]…It is unclear whether cell substrates have a greater or lower risk [of contamination] than other types of cells…However, if their growth in tissue culture is not well controlled, there may be additional opportunities for contamination…” [vi]

And it gets worse.

The same FDA memo goes on to say:

“In addition to the possibility of contamination of cell substrates with adventitious viruses…the use of immortalized, neoplastic human cells to develop [vaccines] raises theoretical concerns with regard to possible contamination with TSE/BSE agents.” [vii]

TSE is Transmissible Spongiform Encephalopathy, a condition that includes a group of rare degenerative brain disorders characterized by tiny holes in the brain tissues, giving a “spongy” appearance when viewed under a microscope. When this condition occurs in cows, it is called Bovine Spongiform Encephalopathy, commonly known as “mad cow disease.” In a study published in 2004, researchers found that any cell line could potentially support the propagation of TSE agents.[viii]

Clearly, CBER is aware and disquieted over the carcinogenic potential of animal cells in vaccines because they require manufacturers to take “every available precautionary step” to eliminate the suspicious cells from the vaccine final product. The FDA also admits concerns about cancer-causing possibility from all types of cell lines. The question begging to be answered is, knowing the potential risks of using cell lines to create vaccines, why is research using cell line technologies allowed to be used at all?

Despite substantial evidence—and even admissions of concern—the FDA appears to be flagrantly ignoring the potential for harm caused by this new cell line technology. The U.S. government have poured billions of dollars into flu shot development and is recklessly approving the use of cell lines for products that have a questionable necessary pandemic vaccine. Let the buyer beware.

[i] “WHO manual on animal influenza diagnosis and surveillance,” World Health Organization, 1 September  2004. http://www.who.int
[ii] Reuters May 19, 2009: http://www.alertnet.org/thenews/newsdesk/LJ556980.htm
[iii] “Influenza Vaccines under development,” Protein Sciences Corporation. http://www.proteinsciences.com/vaccines.htm#rha
[iv] Ledwith, BJ, et al. “Tumorigenicity assessments of Per.C6 cells and of an Ad5-vectored HIV-1 vaccine produced on this continuous cell line.” Dev Biol (Basel). 2006;123:251-63; discussion 265-6.
[v] FDA: Use of MDCK Cells for Manufacture of Inactivated Influenza vaccines. www.fda.gov/ohrms/dockets/ac/05/slides/5-4188S1-1draft.PPT
[vi]“Designer” Cells as Substrates for the Manufacture of Viral Vaccines,” FDA. (http://www.fda.gov/ohrms/dockets/ac/01/briefing/3750b1_01.htm)
[vii] FDA. Ibid MDCK cells.
[viii] Vorberg, I., Raines, A., Story, B., Priola, S. A. “Susceptibility of common fibroblast cell lines to transmissible spongiform encephalopathy agents,” Journal of Infectious Diseases189 (2004): 431–439. PMID: 14745700

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