Kandylini’s

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Posts Tagged ‘vaccines’

Legal immunity set for swine flu vaccine makers

Posted by kandylini on July 20, 2009

Now may be a good time to receive a medical exemption against vaccinations from a sympathetic doctor, in case the government makes life unbearable for those who claim a philosophical or religious exemption. The doctors are  out there—you just have to search around.

Source: Mike Stobbe.

“The last time the government embarked on a major vaccine campaign against a new swine flu, thousands filed claims contending they suffered side effects from the shots. This time, the government has already taken steps to head that off.

Vaccine makers and federal officials will be immune from lawsuits that result from any new swine flu vaccine, under a document signed by Secretary of Health and Human Services Kathleen Sebelius, government health officials said Friday.

“The last time the government faced a new swine flu virus was in 1976. Cases of swine flu in soldiers at Fort Dix, N.J., including one death, made health officials worried they might be facing a deadly pandemic like the one that killed millions around the world in 1918 and 1919.

Federal officials vaccinated 40 million Americans during a national campaign. A pandemic never materialized, but thousands who got the shots filed injury claims, saying they suffered a paralyzing condition called Guillain-Barre Syndrome or other side effects.”

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Old “60 Minutes” Segment on 1976 Swine Flu Vaccine Debacle

Posted by kandylini on July 13, 2009

Source: DailyMotion.com.

This must-see video with Mike Wallace aired on November 4th, 1979. It featured Swine Flu Vaccine victim Judy Roberts, who became paralyzed with Guillian-Barre Syndrome. Although a year later she was able to walk with braces, she didn’t make a full recovery from the vaccine damage.

To add insult to injury, the government dragged its feet in compensating the thousands of victims who contracted Guillian-Barre Syndrome from the vaccine.

This is a good lesson to keep in mind with the latest ManBirdPig Vaccine from Baxter that is coming soon to a school or clinic near you.

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Cervical Cancer Vaccine Paralyses 12-Year-Old Girl

Posted by kandylini on December 14, 2008

Big Pharma stooges, in the guise of modern witch doctors, of course deny any link. Black is white, up is down—parents, ignore the evidence before your very eyes because the “experts” have everything well in hand!

Source: Times Online.

A 12-year-old schoolgirl has been left paralysed from the waist down by a mystery illness that came on 30 minutes after she was given the new anticervical cancer jab.

Ashleigh Cave suffered dizziness and headaches soon after the vaccination at her school and then deteriorated rapidly, collapsing several times over the following days.

A week later she was admitted to hospital after losing all strength in her legs and, two months on, there has been no improvement.

Her mother Cheryl, 37, from Aintree, Merseyside, is blaming her daughter’s condition on the human papillomavirus (HPV) jab, which was introduced in Britain in September as part of a government-funded vaccination programme.

All girls aged 12 and 13 are being offered vaccinations with Cervarix, a drug that stimulates the body to defend itself against HPV, to protect against the later onset of cervical cancer which is linked to the virus.

In America, where an immunisation programme using a similar product, Gardasil, began more than a year earlier, there have been dozens of serious “adverse events” reported in which a link to the vaccinations is suspected.

They included 30 deaths in addition to cases of Guillain-Barré syndrome, an auto-immune disease that can cause paralysis. The American authorities have said, however, that there is no evidence the HPV jabs caused these reactions.

Ashleigh’s case has been logged with Britain’s Medicines and Healthcare products Regulatory Agency as an instance of possible Guillain-Barré syndrome, although her doctors have now apparently ruled it out as the cause.

The agency has also indicated that the illness was probably not caused by the jab. Ashleigh’s doctor at Alder Hey children’s hospital, Liverpool, where she is undergoing tests, has said she did not have a “pathological reaction” to the vaccine.

Cheryl Cave said that she found the timing of her daughter’s symptoms impossible to ignore.

She said that within 30 minutes of Ashleigh having the jab at Maricourt Catholic high school on the morning of October 15, she was complaining of severe headaches and dizziness. Over the next 48 hours her condition worsened and she collapsed five times. Two days later they set off to visit friends in Hampshire but the schoolgirl collapsed again on the train.

She was admitted to Frimley Park hospital in Camberley, Surrey, where doctors gave the initial diagnosis of “vertigo and generalised myalgia, probably due to recent vaccinations”.

On October 22, a week after she was given the HPV jab, she was admitted to Alder Hey hospital, where she has remained ever since.

Her mother said: “At first they tried to tell us she was imagining it because she was being bullied . . . they will not mention her illness and the vaccine in the same sentence.”

A spokesman for the medicines agency said: “Guillain-Barré syndrome naturally occurs in the population. There is no good evidence to suggest that the Cervarix vaccine can cause [it].”

GlaxoSmithKline, which makes Cervarix, said that the agency had suggested the case “was not linked to the vaccine”.

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Flu Vaccination: Docs Talk the Talk Without Walking the Walk

Posted by kandylini on December 11, 2008

Source: ABC News.

Every fall, the public is barraged by messages from doctors, nurses and other health care providers to get a flu vaccination to protect against the influenza virus.

But the truth is, some doctors and nurses might talk the talk without walking the walk.

According to the most recent data from the Centers for Disease Control and Prevention, a significant chunk of health care professionals declined to get vaccinated against the influenza virus during the 2006-07 flu season, with only about 40 percent opting for a jab. It’s an “abysmal and profoundly sad” statistic, according to Dr. William Schaffner, chairman of the department of preventive medicine at Vanderbilt Medical School in Nashville, Tenn.

“Both the professional and ethical responsibility of all health care workers is to be vaccinated annually against influenza,” Schaffner said.

Vaccination serves to protect both patient and health care provider from becoming infected with influenza, as well as from transmitting the contagious virus to others.

Pains, Aches and Chills

One in five Americans get the flu every year, according to the CDC. Of these, 200,000 are hospitalized and about 36,000 die.

Schaffner added that, in the midst of an influenza outbreak, it is crucial to have healthy people on hand to take care of patients.

“We need health care workers on the line delivering medical care,” Schaffner said. “We don’t need them home sick.”

There are legitimate reasons to steer clear of the needle. People with an egg allergy might avoid getting the vaccine because viruses for the flu shot are grown in eggs. People with Guillain-Barre syndrome — a disease that results in nerve damage — should avoid getting vaccinated as well, since respiratory illnesses can trigger an episode.

But for healthy individuals, the CDC recommends that all health care personnel, students in training for those professions, and other high-risk groups such as employees of assisted living communities be vaccinated against the influenza virus.

Professionals make a variety of excuses for not getting the influenza vaccine, chief among which are that they are too busy or that getting vaccinated is inconvenient. Others don’t like needles or believe, mistakenly, that the vaccine will result in a bout of the flu.

To those professionals, Schaffner said, “Get over it.”

No Shot for Me

But for others, a history of good health can justify declining vaccination.

Nancy Ludwick, a registered nurse at Scripps Memorial Hospital in La Jolla, Calif., has had flu vaccinations in the past, particularly after Scripps began to require formal declination for those who chose not to receive the vaccine.

After her last vaccination, Ludwick said she got sick. But this year, Ludwick is experimenting with not getting vaccinated.

“I haven’t had the flu in … [11] years,” Ludwick said. “I don’t like to take anything. I barely take a vitamin. … I’m doing my own trial to see how I would feel or not.”

Ludwick said she feels more protected than the public, since nurses wear gloves and wash their hands constantly.

But experts could be concerned about the ability of doctors and nurses who choose not to get vaccinated to talk up the vaccine to patients.

“If a [person] is not ready to take the vaccine themselves, they are not ready to become an advocate for the vaccine among patients,” Schaffner said.

Still, as a nurse in the intensive care unit at Scripps, Ludwick finds she treats people who are already very sick and cannot handle a flu shot. Overall, Ludwick says staff are encouraged to get vaccinated, rather than required, and that most nurses she works with do.

Work In Progress

Still, the influenza vaccine is not 100 percent effective against the virus.

“We understand that the vaccine is not perfect,” Schaffner said. “But we’re working to make the vaccine better.”

Strong support for getting vaccinated is often the key to achieving vaccination rates above 40 percent.

Dr. David Hooper, chief of the Infection Control Unit at Massachusetts General Hospital in Boston, received his vaccine in October, the beginning of the flu season.

Hooper says he and other administrators encourage hospital staff to get vaccinated through monthly newsletters, updates and by making it as easy as possible to get vaccinated for free by occupational services. The hospital also makes an effort to document who is not getting a flu shot on the premises and who may be getting it elsewhere or not at all.

“A health care worker, annoyingly, could be incubating influenza and transmitting to any number of people,” Hooper said. “Vaccines are the single best public health tool we have for managing influenza.”

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Avoid Flu Shots, Take Vitamin D Instead

Posted by kandylini on December 11, 2008

NOTE: Be sure to take only supplemental D3, cholecalciferol, and not the “vegetarian” version, D2 (ergocalciferol) that’s used in soy milk. For more information, please see Freelearner’s comment below.

After months of supplementing with 4 to 8,000 IU of D3, I’ve notice some positive changes, like feeling more energetic and not getting any colds at all (despite sleeping very little for days at a time).

By Donald W. Miller, Jr., MD.

Another influenza season is beginning in the northern temperate zone, and our government’s Center for Disease Control and Prevention (CDC) will strongly urge Americans to get a flu shot. Health officials will say that every winter 5 – 20 percent of the population catches the flu, 200,000 people are hospitalized, and 36,000 people will die from it.

The CDC’s 15-member Advisory Committee on Immunization Practices (ACIP) makes recommendations each year on who should be vaccinated. Ten years ago, for the 1999 – 2000 season, the committee recommended that people over age 65 and children with medical conditions have a flu shot. Seventy-four million people were vaccinated. Next season (2000 – 01) the committee lowered the age for universal vaccination from 65 to 50 years old, adding 41 million people to the list. For the 2002 – 03 season, the ACIP added healthy children 6 months to 23 months old, and for 2004 – 05, children up to 5 years old. For the 2008 – 09 season the committee has advised that healthy children 6 months to 18 years old have a flu shot each year. Its recommendations for influenza vaccination now covers 256 million Americans – 84 percent of the U.S. population. Only healthy people ages 19 – 49 not involved in some aspect of health care remain exempt. Pharmaceutical companies have made 146 million influenza vaccines for the U.S. market this flu season.

Almost all the ACIP members who make these recommendations have financial ties to the vaccine industry. The CDC therefore must grant each member a conflict-of-interest waiver.

The CDC mounts a well-orchestrated campaign each season to generate interest and demand for flu shots. Along with posters for the public, flyers, and health care provider materials, it encourages doctors to “recommend/urge flu shots.” Medical groups, nonmedical organizations (like the YMCA), and the media trumpet CDC-released messages on influenza, notably: “Flu kills 36,000 per year,” “This could be a bad/serious flu year,” and “Flu vaccine is the best defense against flu.” The government promotes National Vaccination Week, which this year is December 8 – 14. This year, however, rather than uniformly following the government’s “Seven-Step Recipe” for generating demand for flu shots, the mainstream media has questioned their benefits.

The New York Times had an article in the September 2, 2008 issue titled “Doubts Grow Over Flu Vaccine in Elderly,” which says, “The influenza vaccine, which has been strongly recommended for people over 65 for more than four decades, is losing its reputation as an effective way to ward off the virus in the elderly. A growing number of immunologists and epidemiologists say the vaccine probably does not work very well for people over 70, the group that accounts for three-fourths of all flu deaths.” The article refers to a study done by the Group Health Center for Health Studies in Seattle on 3,500 people, age 65 – 94, to determine if flu vaccines are effective in protecting older people against developing pneumonia (Lancet 2008;372:398 – 405).

The National Vital Statistics Reports compiled by the CDC show that only 1,138 deaths a year occur due to influenza alone (257 in 2001, 727 in 2002, 1,792 in 2003, 1,100 in 2004, and 1,812 in 2005). Bacterial pneumonia causes some 60,000 deaths each year, mainly in the winter, when surveillance data show increased prevalence of the flu virus. Using a mathematical (Poisson) regression model, officials estimate that the flu virus triggers some of the winter-time deaths from pneumonia, along with deaths in people with cardiovascular disease and other chronic illnesses. More than 34,000 of those “36,000″ flu deaths are what officials estimate are “influenza-associated” pneumonic and cardiovascular deaths.

The Group Health study reported in the New York Times and other newspapers around the country found that flu shots do not protect elderly people against developing pneumonia. Pneumonia occurs with equal frequency in people over age 65 with or without a flu shot. Earlier studies, biased by the “healthy user effect,” over-estimated the vaccine’s effect on pneumonia because they did not adjust for the presence and severity of other diseases in unvaccinated people. As the Group Health authors point out, “The study found that people who were healthy and conscientious about staying well were the most likely to get an annual flu shot. Those who are frail may have trouble bathing or dressing on their own and are less likely to get to their doctor’s office or a clinic to receive the vaccine. They are also more likely to be closer to death.” Other investigators question that there is a mortality benefit with influenza vaccination. Vaccination coverage among the elderly increased from 15% in 1980 to 65% now, but there has been no decrease in deaths from influenza and pneumonia (Am J Respir Crit Care Med 2008;178:527 – 33). As one vaccine researcher puts it, “I think the evidence base [for mortality benefits from flu shots] we have leaned on is not valid” (Lancet Infect Dis 2007;7:658 – 66).

There is also a lack of evidence that young children benefit from flu shots. A systematic review of 51 studies involving 260,000 children age 6 to 23 months found no evidence that the flu vaccine is any more effective than a placebo (Cochrane Database Syst Rev. 2006;1:CD004879).

Randomized controlled trials are the most reliable way to determine the efficacy – and safety – of a given treatment. No randomized trials show that flu shots reduce mortality from influenza or flu-related pneumonia. Some do show that the flu vaccine is somewhat effective in preventing influenza. In one widely quoted study, 1838 volunteers age 60 and over were randomized to receive a flu shot or placebo (a shot of saline). The flu shot reduced the relative risk of contracting (serologically confirmed, clinical) influenza by a seemingly impressive 50%. The incidence of influenza in the unvaccinated people in this study was 3%. In the vaccinated group it was 2% (JAMA 1994;272:1661 – 5). Flu shots reduced the absolute risk of contracting influenza by a meager 1% (not 50%, as the “relative risk” portrays it). In actuality, for every 100 people that have a flu shot only one will benefit from it – this, in medical parlance, is the “number needed to treat” (NNT) in order to achieve any benefit from the treatment. A flu shot provides no benefit for the other 99 people – 2 of them will get influenza anyway – and all 100 risk being harmed by the vaccine.

Another randomized trial by Zaman and coworkers published recently (NEJM 2008;359: published online September 17, in print October 9) found that the incidence of influenza in infants whose mothers had a flu shot during their pregnancy was 4% (6/159). The incidence of flu in infants whose mothers did not have a flu shot was 10% (16/157). In this study (done in Bangladesh and funded by the Bill and Melinda Gates Foundation, Wyeth Pharmaceuticals, and others) flu shots reduced the relative risk of influenza illness in infants by a seemingly impressive 63%. But only 6 out of 100 infants benefited from the shot. The other 94 received no benefit – 4 got influenza anyway – and all are at risk from being harmed by the vaccine, particularly from the mercury, aluminum, and formaldehyde in it.

After officials select the three strains of flu virus that they think are most likely to be circulating during the next winter season (they picked the wrong ones last year), vaccine makers grow the viruses in fertilized chicken eggs, with 500,000 eggs per day (each examined by hand) for up to eight months. Formaldehyde is used to inactivate the virus. It is a known cancer-causing agent. Aluminum is added to promote an antibody response. It is a neurotoxin that may play a role in Alzheimer’s disease. Other additives and adjuvants in the flu vaccine include Triton X-100 (a detergent), Polysorbate 80, carbolic acid, ethylene glycol (antifreeze), gelatin, and various antibiotics – neomycin, streptomycin, and gentamicin – that can cause allergic reactions in some people.

Two-thirds of the vaccines made for the 2008 – 09 flu season, 100 million of them, contain full-dose thimerosal, an organomercury compound, which is 49% mercury by weight. (An unidentified number of the other 50 million vaccines contain either “no” or “trace” amounts of thimerosal.) It is used to disinfect the vaccine. Each one of these 100 million flu shots contain 25 micrograms of mercury, a mercury content that is 50,000 part per billion, 250 times more than the Environmental Protection Agency’s safety limit. Mercury is a neurotoxin, which has a toxicity level 1,000 times that of lead.

There is some evidence that flu shots cause Alzheimer’s disease. This most likely is a result of combining mercury with aluminum and formaldehyde, which renders them much more toxic together through a synergistic effect than each would be alone. One investigator has reported that people who received the flu vaccine each year for 3 to 5 years had a ten-fold greater chance of developing Alzheimer’s disease than people who did not have any flu shots (Int J Clin Invest 2005;1:1 – 4). (The brains of people with Alzheimer’s disease display three pathologic hallmarks: neurofibillary tangles, amyloid plaques, and phosphorylation of tau protein. Brain cells grown in test tubes develop these changes when exposed to nanomolar doses of mercury, doses similar to the amount of mercury a person gets from a flu shot.)

Mercury in vaccines has also been implicated as a cause of autism. Vaccine makers have now removed thimerosal from all childhood vaccines, except flu shots. For more on this subject see my article “Mercury on the Mind,” with its recommended reading list, and Evidence of Harm: Mercury in Vaccines and the Autism Epidemic: A Medical Controversy by David Kirby.

Three serious, acknowledged adverse reactions to the flu vaccine are joint inflammation and arthritis, anaphylactic shock (and other life-threatening allergic reactions), and Guillain-Barré syndrome. Guillain-Barré syndrome (GBS) is a paralytic autoimmune disease that fells people several weeks after their flu shot. One woman with post-vaccination GBS writes:

“I had a flu shot in November, and by December I became weak and continued to get weaker until I collapsed and was taken to the hospital… I was helpless, totally paralyzed with Guillain-Barré syndrome… I was in ICU for three weeks and then transferred to a rehabilitation center. Three months later I was released to come home because I could ambulate approximately 100 feet with a walker. I continued rehabilitation as an outpatient for the next three months until I could walk with hand crutches. Today, I need a cane. I was not forewarned of any possible hazard when they gave me the flu shot.”

Another:

“I have a friend, now in a wheelchair, who took the flu shot, got Guillain-Barré and now cannot walk.”

Another woman, diagnosed with GBS after a flu shot, spent 16 months in the hospital paralyzed on a ventilator and life support. After several subsequent multi-month hospitalizations she writes:

“On my last visit to my neurologist I was able to walk about 6 feet holding his hand, not much but it took years to be able to do that. I scratch my head when I hear them promoting flu shots… Most people that I come into contact with – in the hospital and out (nurses, doctors, and regular people) – after hearing my story, feel that it is better to chance the flu and not get the shot.” (These statements are in Vaccine Safety Manual for Concerned Families and Health Practitioners: Guide to Immunizations Risks and Protection by Neil Miller [no relation], pages 84 – 86.)

The package inserts that come with the flu vaccine note that GBS is a potential complication. There are 1 to 2 cases of GBS per 1 million vaccinated persons. (There were 10 times that many cases of GBS in 1976 with the flu vaccine used that year). Taking a flu shot is essentially the same as buying a lottery ticket for acquiring Guillain-Barré syndrome.

Seventy percent of doctors do not get a flu shot.

Flu virus exists in people year-round, and new strains seed a population during the “off-season.” In the northern and southern temperate zones, flu epidemics occur in the cold part of the year, October – March and April – September respectively. Flu epidemics occur in the tropics during the rainy season.

Explanations for why flu epidemics occur in the winter when it is cold – people being indoors in close contact, drier air dehydrating mucus and preventing the body from expelling virus particles, the virus lingering longer on exposed surfaces, like doorknobs, with colder temperatures – do not explain why flu epidemics occur in the tropics.

Something that can explain why flu epidemics also occur both in warm and cold climates is this: During a flu epidemic, wherever it may be, the atmosphere blocks ultraviolet B (UVB) radiation from the Sun. In the temperate zones above latitude 35 degrees North and South, the sun is at a low enough angle in the winter that the ozone layer in the atmosphere absorbs and blocks the short-wavelength (280 – 315 nanometers) UVB rays. In the tropics during the wet season, thick rain clouds block UVB rays.

Skin contains a cholesterol derivative, 7-dehydrocholesterol. UVB radiation on skin breaks open one of the carbon rings in this molecule to form vitamin D. The activated form of vitamin D (1,25-dihydroxyvitamin D) attaches to receptors on genes that control their expression, which turn protein production on or off. Vitamin D regulates the expression of more than 1,000 genes throughout the body. They include ones in macrophages, cells in the immune system that, among other things, attack and destroy viruses. Vitamin D switches on genes in macrophages that make antimicrobial peptides, antibiotics the body produces. Like antibiotics, these peptides attack and destroy bacteria; but unlike antibiotics, they also attack and destroy viruses.

Vitamin D also expresses genes that stop macrophages from overreacting to an infection and releasing too many inflammatory agents – cytokines – that can damage infected tissue. Vitamin D, for example, down regulates genes that produce interleukin-2 and interferon gamma, two cytokines that prime macrophages and cytotoxic T cells to attack the body’s tissues. In the 1918 – 19 Spanish flu pandemic that killed 500,000 Americans, young healthy adults would wake up in the morning feeling well, start drowning in their own inflammation as the day wore on, and be dead by midnight, as happened to my 22-year-old grandmother and my wife’s 24-year-old grandmother. Autopsies showed complete destruction of the epithelial cells lining the respiratory tract resulting, researchers now know, from a macrophage-induced severe inflammatory reaction to the virus. In a terribly misguided way, these victims’ own immune system attacked and killed them, not the virus, something in future pandemics vitamin D, in appropriate doses, can prevent.

A creditable hypothesis that explains the seasonal nature of flu is that influenza is a vitamin D deficiency disease. Cannell and colleagues offer this hypothesis in “Epidemic Influenza and Vitamin D” (Epidemiol Infect 2006;134:1129 – 40). They quote Hippocrates (circa 400 B.C.), who said, “Whoever wishes to investigate medicine properly should proceed thus: in the first place to consider the seasons of the year.” Vitamin D levels in the blood fall to their lowest point during flu seasons. Unable to be protected by the body’s own antibiotics (antimicrobial peptides) that this gene-expresser engineers, a person with a low vitamin D blood level is more vulnerable to contracting colds, influenza, and other respiratory infections (e.g., respiratory syncytial virus).

Studies show that children with rickets, a vitamin D-deficient skeletal disorder, suffer from frequent respiratory infections; and children exposed to sunlight are less likely to get a cold. Given vitamin D’s wide-ranging effects on gene expression, other studies, for example, show that people diagnosed with cancer in the summer have an improved survival compared with those diagnosed in the winter (Int J Cancer 2006;119:1530 – 36).

A growing body of evidence indicates that rickets in children and osteomalacia in adults (both a softening of bones due to defective bone mineralization) are just the tip of a vitamin D-deficiency iceberg. Tuberculosis and various autoimmune diseases, such as multiple sclerosis, lupus, and type I diabetes have a causal association with low vitamin D blood levels. Vitamin D deficiency plays a causal role in hypertension, coronary artery disease, congestive heart failure, peripheral vascular disease, and stroke. It is also a risk factor for metabolic syndrome and type II diabetes, chronic fatigue, seasonal affective disorder, depression, cataracts, infertility, and osteoporosis. At the bottom of the vitamin D iceberg lies cancer. There is good evidence that vitamin D deficiency is a causal factor in some 15 different common cancers. (NEJM 2007;357:266 – 81.)

The increased number of deaths that occur in winter, largely from pneumonia and cardiovascular diseases, are much more likely due to vitamin D deficiency than to an increased prevalence of serologically-positive influenza virus (which also results from vitamin D deficiency).

Experts reckon that an optimum blood level of vitamin D (25-hydroxyvitamin D) is 50 – 99 ng/ml. (Children need a blood level >8 ng/ml to prevent rickets. It takes a concentration >20 to maintain parathyroid hormone levels in a normal range. A level >34 is needed for peak intestinal calcium absorption. And in elderly people neuromuscular performance steadily improves as vitamin D blood levels rise to 50 ng/ml.) The government’s recommended daily allowance (RDA) for vitamin D is 400 IU (international units) a day, an amount sufficient to prevent rickets and osteomalacia but not vitamin D’s other gene-regulating benefits. To achieve all of vitamin D’s benefits one has to take an amount ten times the government’s RDA – 4,000 to 5,000 IU a day.

A light-skinned person will synthesize 20,000 IU of vitamin D in 20 minutes sunbathing on a tropical beach, at which point vitamin D synthesis shuts down for the day (it takes a dark-skinned person 6 to 10 times longer to make this amount). Human breast milk does not contain vitamin D, since, from an evolutionary standpoint, our African ancestors’ infants, reared near the equator, could readily synthesize this gene regulator from sunlight in their skin. Food contains very little vitamin D. (The highest concentrations are in wild salmon, mackerel, sardines, and cod liver oil.) Federal regulations now require that some foods, like milk, be fortified with vitamin D. But one would have to drink 200 glasses of milk to obtain the amount of vitamin D a light-skinned person can make in 20 minutes sunbathing.

The majority of Americans are vitamin D deficient, with a 25-hydroxy D blood level <20 ng/ml, or insufficient, with a level of 20 – <30 ng/ml. Cheap vitamin D supplements (D3, not D2) provide the only way most of us can maintain a year-round vitamin D blood levels greater than 50 ng/ml. That requires taking 4 – 5,000 IU of vitamin D a day (50,000 IU every ten days or 150,000 IU a month).

Taking vitamin D in these doses is safe, far safer than a flu shot with all the bad chemicals it contains. Concerns about vitamin D toxicity are overblown. One can take a 10,000 IU vitamin D supplement on a daily basis without any adverse effects. In healthy persons, long-term consumption of more than 40,000 IU a day is necessary to cause an elevation in the blood calcium level (hypercalcemia), the first manifestation of vitamin D toxicity (Am J Clin Nutr 2006;84:694 – 97). Check your vitamin D (25-hydroxy D) blood level. People with granulomatous diseases like sarcoidosis should also check their blood level of 1,25-dihydroxyvitamin D, the active form.

Can a shot (or tablets) of vitamin D prevent influenza better than a flu shot? There is good reason to believe that it can.

Doctors in India and Canada give people a once-yearly injection of 600,000 IU of vitamin D (MJA 2005;183:10 – 12). That would be better, and safer, than having a flu shot. Daily, weekly, or monthly vitamin D tablets work just as well. For more on this subject see my article “Vitamin D in a New Light” and visit Dr. Cannell’s Vitamin D Council website.

Investigators have completed one double-blind, randomized, placebo-controlled trial that shows vitamin D prevents colds and influenza significantly better (P <0.002) than a placebo pill (Epidemiol Infection 2007;135:1095 – 6). A large multi-center randomized trial conducted over multiple flu seasons comparing vitamin D to a flu shot can show conclusively which is better, and safer. But given the financial stakes underpinning flu shots, and unpatentable vitamin D, who will fund it?

In the meantime, considering what is most likely to be the outcome of such a trial, if it is ever conducted, I recommend that you avoid flu shots and take vitamin D instead.

Notes

Influenza virus Flu viruses are classified into types A, B, and C. Type A viruses cause most influenza epidemics. They exist, replicate, and mutate in swine and horses; seals, dolphins, and whales; migratory water birds, geese and ducks; domestic birds chicken and turkeys; and humans. Type B and C viruses exist only in humans and only type B causes (relatively mild) infections. Influenza A viruses are further categorized into subtypes on the basis of two surface antigens (proteins): hemaglutinin (H) and neuraminidase (N). There are 15 different H and 9 different N antigens. The 1918 – 19 Spanish flu pandemic was caused by an H1NI Type A virus. Subtypes of influenza viruses are further classified by the names of cities, states or countries, along with the year they were discovered. For the 2008 – 09 (northern temperate zone) season, officials predict and have directed vaccines to be made against A/Brisbane/59/2007 (H1N1), A/Brisbane/10/2007 (H3N2), and B/Florida/4/2006. In an unusual departure, they are all different from the previous season, which missed the strains that caused influenza that season. What doctors diagnose as “influenza” is often an influenza-like illness caused by a respiratory virus other than the flu. Serologic tests are necessary to prove that one’s respiratory illness is actually caused by the flu virus.

Other things to do to prevent the flu: Avoid sugar. It suppresses immunity. Avoid Omega-6 vegetable oils (corn, safflower, sunflower, peanut, canola, and soybean oil). Americans consume 50 times more of these oils than are necessary for good health. In this amount they are powerful immune suppressants. Take a well-balanced multivitamin/mineral capsule on a daily basis. Eat garlic. Manage stress. Exercise. Get enough rest. And wash your hands. Viruses spread most often from touching contaminated objects, like doorknobs, phones, shared computer keyboards, and shaking hands.

Donald Miller (send him mail) is a cardiac surgeon and Professor of Surgery at the University of Washington in Seattle. He is a member of Doctors for Disaster Preparedness and writes articles on a variety of subjects for LewRockwell.com. His web site is www.donaldmiller.com

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Genetically engineered Merck Cancer Vaccine Made Mandatory For Immigrants

Posted by kandylini on September 17, 2008

By Steve Watson, Infowars.net.

Immigrants seeking permanent legal residency in the U.S. are now mandated to take an expensive and controversial vaccine that has been linked with thousands of serious complaints and several deaths.

The Human Papillomavirus (HPV) vaccine — known as Gardasil — is one of five the U.S. Citizenship and Immigration Services recently added to the required list, reports Fox 8 News.

A press release from the U.S. Citizenship and Immigration Services Agency confirms that the requirements for the vaccine went into effect on July 1, 2008.

The regulation represents a total dismissal of the recommendation of Dr. Jon Abramson, chairman of the Centers for Disease Control and Prevention’s advisory committee on immunization practices. In February 2007, Abramson said that he and the 15-member panel at the CDC opposed making Gardasil mandatory because the sexually transmitted HPV is not a contagious disease like measles or chicken pox.

At $162 per dose, the three-dose vaccine is set to make millions in profits for Gardasil manufacturer Merck, a company that has a history of both lobbying intensely for state mandates and entering into crony deals to hoodwink Americans into believing HPV vaccinations are compulsory.

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“Conclusive” vaccination study?

Posted by kandylini on September 5, 2008

This is regarding the study that came out that supposedly found no link between autism and the MMR vaccine. No wonder there were so many news stories about parents who don’t vaccinate against measles a couple of weeks ago! This is a classic set-up. I’ll bet “they” hope it reassures the questioning sheeple that all is well in Vaccine Land.

Source: TampaBay10.com.

St. Petersburg, Florida—A local pediatrician, who treats many young patients with autism, is speaking out against a new government study on childhood MMR vaccinations.

The Centers for Disease Control released a new study, claiming there is no link between the combination Measles-Mumps-Rubella (MMR) vaccine and autism nor gastrointestinal disorders.

While several researchers said this study is “conclusive” proof that there is no link, Tampa pediatrician, Dr. David Berger says the study is too small (38 children) to make that claim and not comprehensive enough to give parents 100 percent assurance.

Dr. Berger says larger, longterm studies are needed.

The Tampa board certified pediatrician advises parents to separate the live combination virus vaccine so they can tell if their child has had an allergic reaction to any of the vaccines. That will help parents when it comes time to give kids their MMR booster shot around kindergarten.

Dr. Berger says he uses the same cautious approach when it comes to introducing new foods to kids, try one at a time.

Many parents of autistic kids and advocacy groups suspect that combination MMR vaccine may have triggered their child’s GI (gastrointestinal) disease and autism, but there are no longterm studies to support that claim.

Watch Heather’s story on “Why some Bay area parents are separating combination MMR vaccines.”

Click here to find a pediatrician or location that will separate vaccines.

Here is Dr. David Berger’s online interview:

-What is your reaction to this study?

If this study was done in an attempt to try and replicate the original research that was done by Dr. Wakefield, the researchers completely missed the point.

Dr. Wakefield specifically looked at children- who had developed symptoms of both autism and intestinal abnormalities after receiving the MMR vaccine, and in those particular patients he was able to identify the presence of the measles virus.

In this current study 80% of the patient’st had abnormal gastrointestinal symptoms prior to receiving MMR.

-Do you agree this study is conclusive of no link?

It is not possible for a study such as this to be conclusive . There was a small sample size, for one thing. I guess that one could conclude that the evidence from the study shows that the small group of children studied who have abnormal intestinal symptoms prior to getting the vaccine do not show evidence of measles in the intestinal tract, but I think it would be reaching to go further than that .

-Does this put the controversy to rest?

Absolutely not.

-What are your concerns about this study?

As stated above.

Also, this study is only looking for presence of the measles virus itself. We know that there are immunological changes that occur when a person is injected with a virus which is different than what happens when a virus is either inhaled or ingested. These immunological changes may persist, and it can be independent of the virus itself persisting.

-What are you advising cautious parents to do?

Follow their instincts

-The government claims there are many studies proving no link and combination MMR is safe. Do you believe these studies are adequate?

I do not.

-What type of study is needed?

Someone needs to replicate Dr. Wakefield study done in the exact same manner that he did.

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Gardasil Meets Measles: A Coincidence?

Posted by kandylini on August 29, 2008

I had a feeling there was some ulterior motive behind the reporting of the “high” rate of measles outbreak last week.

by Barbara Loe Fisher

www.vaccineawakening.blogspot.com
www.NVIC.org
www.StandUpBeCounted.org
http://www.vran.org/vaccines/hpv/hpv.htm

The bad news about GARDASIL vaccine keeps getting worse and it was only a matter of time before government health officials promoted an “epidemic” to deflect attention from GARDASIL risks and create an excuse to point accusing fingers at parents who decline to give their children one or more of the 16 federally promoted vaccines. They did the same thing in 1985, when publicity about DPT vaccine reactions prompted officials at the CDC and American Academy of Pediatrics to allege there were whooping cough epidemics in eight states due to parents rejecting DPT. Then as now, the cases of disease were divided between vaccinated and unvaccinated children and adults, which is hardly big news.

The government’s dire warnings came late last week after newspaper articles examined the muscle that Merck used to get GARDASIL fast tracked and licensed, followed by an aggressive multi-media advertising and lobbying campaign targeting teenage girls which has already netted the big pharmaceutical company more than $1.5 billion in sales worldwide. The New England Journal of Medicine published an editorial discussed in the Wall Street Journal asking good questions about the evidence for long term protection and cost effectiveness of mass use of GARDASIL vaccine, questions that NVIC first raised in 2007 .
And new concerns are being voiced about whether the vaccine is safe to give to adolescent girls , whose bodies are undergoing hormonal changes, as no studies have been published to evaluate whether there are increased risks for vaccine reactions depending upon when the vaccine is administered during a girl’s monthly hormonal cycle.

Last week, a CDC apparently weary of all the bad publicity about GARDASIL got its taxpayer-funded PR machine in gear and issued a media advisory warning that 131 cases of measles have been reported in the U.S. this year and that half of those cases involved unvaccinated children whose parents homeschooled their children or held religious or philosophical beliefs opposing use of one or more vaccines. National news stories and local news coverage examined the measles outbreaks and allegations of growing parental vaccine refusal.

The New York Times published an editorial and repeated unsubstantiated claims made by the CDC about the numbers of children, who were injured and died from measles in the past, stating that there were 400-500 deaths; 48,000 hospitalizations and 1,000 cases of brain injury out of 3-4 million measles cases every year prior to mass use of measles vaccine. A quick look at MMWR historical charts reveals that the highest number of reported cases of measles in the U.S. since 1945 (and before the measles vaccine was licensed in 1963) was 763,094 cases in 1958. Why don’t CDC officials publicly release the documented cases of hospitalization, injury and death due to measles in that year – or ANY year – instead of demanding blind faith in their version of the facts? (For decades, parents have been waiting for the CDC to document the widely published allegation that there are “36,000 deaths” due to influenza every year in the U.S., a statistic that is promoted to justify new directives that every baby and child through age 18 get annual flu shots.)

The publicizing of 131 cases of measles out of a population of 300 million people in the U.S. and blaming the “outbreak” on 63 cases that occurred in unvaccinated children, whose parents hold religious or conscientious objections to vaccination or homeschool, is a transparent attempt by federal employees to persecute fellow citizens holding religious beliefs, moral convictions, intellectual positions and wellness lifestyles different from their own. Adopting a strategy that “the best defense is a good offense,” CDC officials are whipping up fear of those who do not vaccinate in order to cover up a three decade refusal to scientifically investigate reports of children regressing into autism and other kinds of chronic illness after administration of MMR and other vaccines. They know the truth about vaccine risks is becoming more widely known and are lobbying hard for removal vaccine exemptions they do not control so all Americans will be forced without exception to get every vaccine marketed by industry and mandated by government officials.

The premature licensure and universal use recommendation of GARDASIL is just the latest example of what is wrong with the mass vaccination system. If there is a crisis of confidence in the safety of vaccines, which prompts parents to ask pediatricians more questions and seek alternative health care options for keeping their children well, that crisis of confidence can be laid squarely at the feet of those operating the mass vaccination system for failing to do their job. As Generation Rescue founder J.B. Handley recently commented, “Most parents I know will take measles over autism.

There is a 92 to 100 percent uptake of MMR vaccine and many other federally recommended childhood vaccines among children entering kindergarten in every state. This is one of the highest vaccination rates in the world, especially in such a large population. If the MMR vaccine is so unreliable that a few hundred cases or even a few thousand cases of measles among 300 million people is a cause for panic, then the benefits of MMR vaccine weighed against its risks are far less than industry, government and medical organizations have admitted.

In the 1960’s, when the live virus measles vaccine was licensed, parents were told it would give their babies the same lifelong immunity that having the natural disease confers. By the late 1980’s, it was clear that was not true because measles was occurring in both vaccinated and unvaccinated children. Government officials eventually recommended another dose of measles vaccine (usually given as MMR) for all children even though there were outstanding questions about the multiplication of different genetic strains of measles and how this may affect the vaccine’s ability to prevent measles on an individual and population basis long term.

Today’s young mothers do not have qualitatively superior measles antibodies to transfer to their newborns to protect them in the first year of life as past generations of mothers did because most young mothers giving birth today have been vaccinated and never had measles as children, which confers lifelong immunity. So babies born today are vulnerable to measles from birth instead of from ages 15 months to six years, which is when most children in the past experienced measles by age six and severe complications were rare. For several decades, vaccinologists have been attempting to create a “high titer” EZ measles vaccine that can be given to infants under one year that will override any existing natural maternal antibodies and replace them with vaccine induced antibodies but there have been long-standing questions about EZ measles vaccine safety .

Vaccination does not mimic the natural disease process and offers only temporary immunity, which is why vaccine boosters are frequently given. Every vaccine carries a reaction risk that can be greater for some than others. Measles vaccine, which is part of the combination live virus MMR (measles-mumps- rubella) vaccine can cause brain inflammation and permanent brain damage . There have been more than 46,000 reports of health problems associated with MMR vaccination made to the federal Vaccine Adverse Events Reporting System (VAERS) . However, there is gross underreporting of vaccine- related health problems to VAERS and it is estimated that, for example, fewer than 4 percent of all cases of thrombocytopenia (potentially fatal blood disorder) following MMR vaccination are ever reported to VAERS.

The CDC’s one-size-fits-all, no-exceptions MMR vaccine policies allow almost no contraindications to MMR vaccine use. According to the CDC, a child can be sick at the time of vaccination or recovering from an illness; have a fever; be taking antibiotics; have a history of allergies; or have experienced a seizure or regression after a previous MMR shot and still be eligible for more MMR vaccine. This kind of cavalier disregard for minimizing vaccine risks is one reason why more parents are questioning government vaccine policies.

Parents, whether they do or do not vaccinate their children, should become informed and clearly understand the symptoms and complications of every infectious disease, including measles. Parents who choose to vaccinate should have a 99 to 100 percent guarantee that the vaccine will, indeed protect their child. They should have a similar guarantee that the vaccine will not injure or kill their child.

Like all pharmaceutical products, vaccines should be subject to the law of supply and demand. When people are captive and unable to make informed, voluntary decisions about vaccines that have been rushed to market on greased skids by federal health agencies, where every vaccine reaction is unscientifically labeled a “coincidence,” the first casualty is freedom and the second is the health of innocent children.

Public health officials and pediatricians should explain why 20 percent of America’s highly vaccinated child population suffers with chronic illness and disability rather than blaming parents who refuse to salute smartly and take the risk of watching the child they love become one more victim of vaccine damage.

To report a vaccine reaction to NVIC’s Vaccine Reaction Registry , go to http://www.nvic.org/Report/reaction.htm .

To view vaccine reaction reports, go to the Vaccine VictimMemorial at http://vaccinememorial.org/
__________________________________________

“Ms. Kim and Harvard colleague Sue Goldie concluded that it cost about $43,600 per “quality- adjusted life year” gained, when HPV vaccine is administered to 12-year-old girls. This falls below the $50,000 per quality-adjusted life year threshold that some researchers use as a maximum for cost- effectiveness. Other researchers use a higher maximum benchmark of $100,000 per QALY to gauge cost-effectiveness….. At least one of the factors in the primary Harvard calculations may be a relatively optimistic assumption — that vaccination would produce lifelong immunity. Because the vaccine was only studied for five years and has been on the market for two years, no one knows for certain if its protection is lifelong, or if it wanes over time. The Harvard researchers concluded that the cost per QALY would rise if the vaccine’s effect wanes after 10 years. Merck says the vaccine will offer protection well beyond five years, Dr. Haupt said. The Merck economic model that arrived at the cost per QALY below $50,000 assumed lifelong immunity, he said. Still, the study is likely to fuel skepticism about Gardasil, which has already faced questions surrounding its safety and effectiveness (Merck and the CDC maintain it is safe and effective, with the most common side effect being soreness at site of injection.)” – Peter Loftus, Wall Street Journal (August 21, 2008) http://online.wsj.com/article/SB121928503311259059.html?mod=googlenews_wsj

“Why has there not been any mention of the potentially adverse effects of Merck’s cervical cancer vaccination, Gardasil® in relationship to the timing of the vaccination and where a young woman is in her menstrual cycle? This information is especially critical considering the vaccination is recommended for adolescent girls from the age of nine to young women up to 26-years. Why is it that women are constantly forced into a male medical model which blatantly ignores their menstrual health and administers drugs, surgeries, and vaccinations without any regard to where women are in their hormone cycle?….As the female hormone levels of estrogen and progesterone decrease during the premenstrual phase, the female body begins the process of releasing the uterine lining in the act of menstruation. The decrease in hormones actually affects a woman’s energy levels and her emotions. The immune system becomes more compromised, and that translates to a lowered defense system to fight off invading, foreign toxins….. In her 1977 groundbreaking book, “The Premenstrual Syndrome”, Katharina Dalton noted that drug reactions “…..are common during the premenstruum and may follow administration of antibiotics and inoculations. Confusion may occur as to the real origin of such reactions. In double-blind, clinical trials the placebo drugs are often reported to have side effects such as increased drowsiness, headache, nausea, or increased pain; which may be no more than the usual premenstrual symptoms which have not been meticulously observed and reported.” – Leslie Carol Botha and H. Sandra Chevalier-Batik, Holy Hormones (August 21, 2008)
http://holyhormones.com/about-2/articles-by-leslie/now-hold-on-one-hormonal-minute%E2%80%A6/

“Measles cases in the U.S. are at the highest level in more than a decade, with nearly half of those involving children whose parents rejected vaccination, health officials reported Thursday. Worried doctors are troubled by the trend fueled by unfounded fears that vaccines may cause autism. The number of cases is still small, just 131, but that’s only for the first seven months of the year. There were only 42 cases for all of last year…..The CDC’s review found that a number of cases involved home-schooled children not required to get the vaccines. Others can avoid vaccination by seeking exemptions, such as for religious reasons…..The vaccine is considered highly effective but not perfect; 11 of this year’s cases had at least one dose of the vaccine. Of this year’s total, 122 were unvaccinated or had unknown vaccination status. Some were unvaccinated because the children were under age 1 – too young to get their first measles shot. In 63 of those cases – almost all of them 19 or under – the patient or their parents refused the shots for philosophical or religious reasons, the CDC reported. In Washington state, an outbreak was traced to a church conference, including 16 school-aged children who were not vaccinated. Eleven of those kids were home schooled and not subject to vaccination rules in public schools. It’s unclear why the parents rejected the vaccine. The Illinois outbreak – triggered by a teenager who had traveled to Italy – included 25 home-schooled children, according to the CDC report.” – Mike Stobbe, Associated Press (August 21, 2008)
http://news.yahoo.com/s/ap/20080821/ap_on_he_me/med_measles_outbreaks

“He was advanced for his age. He was talking when he was 11 months old,” recalls Edward Delean. The father of 4 says everything changed after his now 9 year old son who has autism was vaccinated against measles, mumps, and rubella or MMR. It was like that was it. He never talked again, he still doesn’t talk. He has about 10 words,” he says, adding, “it really devastated our family. I just destroyed us.” Testimonials like that have led some parents to shun vaccinations altogether. The Centers for Disease Control says measles cases have dramatically increased from 42 cases in all of last year to 131 in just the first seven months of this year because of parents who are rejecting the MMR vaccine for their kids. “It doesn’t serve us well when we have government officials trying to create fear and anxiety” says Barbara Loe Fisher with the National Vaccine Information Center. She says some parents opt out of immunizations for religious or philosophical reasons. Others have said no because their kids have had adverse reactions to the vaccines that are usually given on a set schedule. “Right now we’re seeing a one-size fits all approach to vaccination that doesn’t really recognize that children are different, that children react differently to vaccinations,” she says.” – Nancy Yamada, WUSA9-TV (August 21, 2008)
http://www.wusa9.com/news/health/story.aspx?storyid=75284&catid=28

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Drugs.com Lists “Autism” as Known Adverse Reaction to DTaP Vaccine Tripedia

Posted by kandylini on August 7, 2008

From Adventures in Autism:

In Drugs.com’s “A to Z Drug Facts” section the entry on Diphtheria / Tetanus Toxoids / Acellular Pertussis Vaccine contains the following Central Nervous System Adverse reactions for Sanofi Pasteur’s Tripedia:

Tripedia
Drowsiness (29%); irritability (25%); anorexia (10%); fussiness (6%); autism, convulsion, encephalopathy, grand mal convulsion, hypotonia, neuropathy, somnolence (postmarketing).”

Hats off to Drugs.com for actually providing informed consent to consumers. To my knowledge they are the first to do it.

HT: Allison Chapman

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12 Babies from Poor Families Die in Glaxo Vaccine Trials

Posted by kandylini on July 14, 2008

Source: Trading Markets.

Buenos Aires, Jul 10, 2008

At least 12 babies who were part of a clinical study to test the effectiveness of a vaccine against pneumonia have died over the past year in Argentina, the local press reported Thursday.

The study was sponsored by global drug giant GlaxoSmithKline and uses children from poor families, who are “pressured and forced into signing consent forms,” the Argentine Federation of Health Professionals, or Fesprosa, said.

“This occurs without any type of state control” and “does not comply with minimum ethical requirements,” Fesprosa said.

The vaccine trial is still ongoing despite the denunciations, and those in charge of the study were cited by the Critica newspaper as saying that the procedures are being carried out in a lawful manner.

Colombian and Panama were also chosen by GSK as staging grounds for trials of the vaccine against the pneumococcal bacteria.

Since 2007, 15,000 children under the age of one from the Argentine provinces of Mendoza, San Juan and Santiago del Estero have been included in the research protocol, a statement of what the study is trying to achieve.

Only 12 have died throughout the country, which is a very low figure if we compare it with the deaths produced by respiratory illnesses caused by the pneumococcal bacteria,” pediatrician Enrique Smith, one of the lead investigators, said.

In Santiago del Estero, one of the country’s poorest provinces, the trials were authorized when Enrique’s brother, Juan Carlos Smith, was provincial health minister.

According to pediatrician Ana Maria Marchese, who works at the children’s hospital in the provincial capital where the studies are being conducted, “because they can’t experiment in Europe or the United States, they come to do it in third-world countries.”

“A lot of people want to leave the protocol but aren’t allowed; they force them to continue under the threat that if they leave they won’t receive any other vaccine,” said Julieta Ovejero, great aunt of one of the six babies who died in Santiago del Estero.

Fesprosa’s Juan Carlos Palomares said that “in most cases these are underprivileged individuals, many of them unable to read or write, who are pressured into including their children” in the trials.

According to Fesprosa, “the laboratory pays $8,000 for each child included in the study, but none (of that money) remains in the province that lends the public facilities and the health personnel for the private research.”

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