Category Archives: Medical Mafia

3D-Printed Human Embryonic Stem Cells Created for First Time

3d-printed-stem-cells.jpg1360072001
Scientists used 3D printing to form these aggregates of embryonic stem cells, shown here at 24 hours (left) and 48 hours (right) after printing.

LiveScience.com | Feb 6, 2013

By Tanya Lewis

Imagine if you could take living cells, load them into a printer, and squirt out a 3D tissue that could develop into a kidney or a heart. Scientists are one step closer to that reality, now that they have developed the first printer for embryonic human stem cells.

In a new study, researchers from the University of Edinburgh have created a cell printer that spits out living embryonic stem cells. The printer was capable of printing uniform-size droplets of cells gently enough to keep the cells alive and maintain their ability to develop into different cell types. The new printing method could be used to make 3D human tissues for testing new drugs, grow organs, or ultimately print cells directly inside the body.

Human embryonic stem cells (hESCs) are obtained from human embryos and can develop into any cell type in an adult person, from brain tissue to muscle to bone. This attribute makes them ideal for use in regenerative medicine — repairing, replacing and regenerating damaged cells, tissues or organs. [Stem Cells: 5 Fascinating Findings]

In a lab dish, hESCs can be placed in a solution that contains the biological cues that tell the cells to develop into specific tissue types, a process called differentiation. The process starts with the cells forming what are called “embryoid bodies.” Cell printers offer a means of producing embryoid bodies of a defined size and shape.

In the new study, the cell printer was made from a modified CNC machine (a computer-controlled machining tool) outfitted with two “bio-ink” dispensers: one containing stem cells in a nutrient-rich soup called cell medium and another containing just the medium. These embryonic stem cells were dispensed through computer-operated valves, while a microscope mounted to the printer provided a close-up view of what was being printed.

The two inks were dispensed in layers, one on top of the other to create cell droplets of varying concentration. The smallest droplets were only two nanoliters, containing roughly five cells.

The cells were printed onto a dish containing many small wells. The dish was then flipped over so the droplets now hung from them, allowing the stem cells to form clumps inside each well. (The printer lays down the cells in precisely sized droplets and in a certain pattern that is optimal for differentiation.)

Tests revealed that more than 95 percent of the cells were still alive 24 hours after being printed, suggesting they had not been killed by the printing process. More than 89 percent of the cells were still alive three days later, and also tested positive for a marker of their pluripotency — their potential to develop into different cell types.

Biomedical engineer Utkan Demirci, of Harvard University Medical School and Brigham and Women’s Hospital, has done pioneering work in printing cells, and thinks the new study is taking it in an exciting direction. “This technology could be really good for high-throughput drug testing,” Demirci told LiveScience. One can build mini-tissues from the bottom up, using a repeatable, reliable method, he said. Building whole organs is the long-term goal, Demirci said, though he cautioned that it “may be quite far from where we are today.”

Others have created printers for other types of cells. Demirci and colleagues made one that printed embryonic stem cells from mice. Others have printed a kind of human stem cells from connective tissues, which aren’t able to develop into as many cell types as embryonic stem cells. The current study is the first to print embryonic stem cells from humans, researchers report in the Feb. 5 issue of the journal Biofabrication.

DARPA produces 10 million flu vaccine doses in one month

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Tobacco plants used in the development of the vaccine

**Editor’s Warning: This article is highly infectious military/industrial/medical propaganda. Read at own risk. Take necessary precautions.**

gizmag.com | Jan 26, 2013

By David Szondy

A familiar news topic during the flu season is the difficulties that the authorities face in producing enough flu vaccine fast enough to control the outbreak. That’s a serious enough problem, but when the influenza outbreak turns out to be the start of a global pandemic, then hundreds of millions of lives could be at risk. To combat this, the Defense Advanced Research Projects Agency (DARPA) has developed a new way of making vaccines that has turned out 10 million doses of H1N1 influenza vaccine in a month, in a recent test run.

A globalized world means a world increasingly at risk from pandemic diseases. According to the World Health Organization (WHO), 20 to 50 percent of the world’s population is at risk from a pandemic outbreak such as that seen in the influenza epidemic of 1918. US military forces are particularly vulnerable because the nature of military life is perfect for the spread of disease, unless countermeasures such as cleanliness and vaccinations are constantly employed.

The problem is, vaccines for new diseases can’t be produced quickly. According to WHO, it can take up to nine months to develop and put a vaccine into production. Worse, egg-based and other conventional vaccine production techniques may not be able to scale up sufficiently to meet the demand – especially for diseases where two doses per person are required for adequate protection.

DARPA’s approach to solving this is the Blue Angel program. Started in response to the 2009 H1N1 swine flu pandemic, its purpose is to quickly develop practical countermeasures to disease outbreaks due to either natural causes or biowarfare attack. The program has a number of aspects, such as finding ways to identify people who are infected before symptoms show, but one major facet is the Accelerated Manufacture of Pharmaceuticals (AMP) project.

Working with Medicago Inc., AMP uses tobacco plants instead of eggs to produce recombinant proteins that are key to vaccines. According to the company, introducing viral genes into tobacco has a number advantages: the full-grown plants can be used because the protein is produced in the leaves; it avoids the need to procure eggs in huge quantities; and, there’s no danger of the virus killing the egg embryo. Medicago said that the tobacco process can generate the proteins within 14 days of the gene sequence of the virus being identified, with vaccine-grade proteins generated within four weeks. In the DARPA tests, 10 million doses of H1N1 influenza vaccine were produced in one month, as defined by an animal model.

According to DARPA, third party testing confirmed that a single dose in an animal model produced hemagglutinin antibodies at a protective strength. However, only clinical trials can determine how effective it would be on humans, and the entire process still needs FDA approval.

Bill Gates Says Global Vaccination Program is “God’s Work”

bill gates malaria vaccines
Dees Illustration

Activist Post | Jan 25, 2013

by Brandon Turbeville

In a recent interview with the London Telegraph, Bill Gates has now claimed that his Foundation’s massive push for vaccination is not just an exercise in philanthropy but that it is, in fact, “God’s work.”

Gates, who, according to the Telegraph, is worth an estimated $65 billion, is now dedicating his life to the “eradication of poliomyelitis,” or, at least he is dedicating himself to the vaccination program allegedly aimed at achieving these ends.

As reported by the Telegraph,

“My wife and I had a long dialogue about how we were going to take the wealth that we’re lucky enough to have and give it back in a way that’s most impactful to the world,” he says. “Both of us worked at Microsoft and saw that if you take innovation and smart people, the ability to measure what’s working, that you can pull together some pretty dramatic things.

“We’re focused on the help of the poorest in the world, which really drives you into vaccination. You can actually take a disease and get rid of it altogether, like we are doing with polio.”

Yet, eradicating polio through a massive vaccination program may be easier said than done writes Neil Tweedie of the Telegraph. “There is another, sinister obstacle: the propagation by Islamist groups of the belief that polio vaccination is a front for covert sterilisation and other western evils. Health workers in Pakistan have paid with their lives for involvement in the programme.”

To this question, Gates responded with seemingly atypical religious zeal, noted by Tweedie in the published article. “It’s not going to stop us succeeding,” says Gates. “It does force us to sit down with the Pakistan government to renew their commitments, see what they’re going to do in security and make changes to protect the women who are doing God’s work and getting out to these children and delivering the vaccine.”

Read More

 

“Medical tragedy”: Swine flu shot linked to narcolepsy, nightmares, hallucinations, sleep paralysis and cataplexy

Emelie Olsson falls asleep as he watches television in her apartment in Stockholm
Emelie Olsson is plagued by hallucinations and nightmares. When she wakes up, she’s often paralyzed, unable to breathe properly or call for help. During the day she can barely stay awake, and often misses school or having fun with friends. She is only 14, but at times she has wondered if her life is worth living.

Stiernstedt says Sweden’s mass vaccination saved between 30 and 60 people from swine flu death. Yet since the pandemic ended, more than 200 cases of narcolepsy have been reported in Sweden.

Reuters | Jan 22, 2013

By Kate Kelland, Health and Science Correspondent

STOCKHOLM – Emelie Olsson is plagued by hallucinations and nightmares. When she wakes up, she’s often paralyzed, unable to breathe properly or call for help. During the day she can barely stay awake, and often misses school or having fun with friends. She is only 14, but at times she has wondered if her life is worth living.

Emelie is one of around 800 children in Sweden and elsewhere in Europe who developed narcolepsy, an incurable sleep disorder, after being immunized with the Pandemrix H1N1 swine flu vaccine made by British drugmaker GlaxoSmithKline in 2009.

Finland, Norway, Ireland and France have seen spikes in narcolepsy cases, too, and people familiar with the results of a soon-to-be-published study in Britain have told Reuters it will show a similar pattern in children there.

Flu vaccination ban goes national after fever, convulsions in children

Their fate, coping with an illness that all but destroys normal life, is developing into what the health official who coordinated Sweden’s vaccination campaign calls a “medical tragedy” that will demand rising scientific and medical attention.

Europe’s drugs regulator has ruled Pandemrix should no longer be used in people aged under 20. The chief medical officer at GSK’s vaccines division, Norman Begg, says his firm views the issue extremely seriously and is “absolutely committed to getting to the bottom of this”, but adds there is not yet enough data or evidence to suggest a causal link.

Others – including Emmanuel Mignot, one of the world’s leading experts on narcolepsy, who is being funded by GSK to investigate further – agree more research is needed but say the evidence is already clearly pointing in one direction.

“There’s no doubt in my mind whatsoever that Pandemrix increased the occurrence of narcolepsy onset in children in some countries – and probably in most countries,” says Mignot, a specialist in the sleep disorder at Stanford University in the United States.

30 MILLION RECEIVED PANDEMRIX

In total, the GSK shot was given to more than 30 million people in 47 countries during the 2009-2010 H1N1 swine flu pandemic. Because it contains an adjuvant, or booster, it was not used in the United States because drug regulators there are wary of adjuvanted vaccines.

GSK says 795 people across Europe have reported developing narcolepsy since the vaccine’s use began in 2009.

Questions about how the narcolepsy cases are linked to Pandemrix, what the triggers and biological mechanisms might have been, and whether there might be a genetic susceptibility are currently the subject of deep scientific investigation.

But experts on all sides are wary. Rare adverse reactions can swiftly develop into “vaccine scares” that spiral out of proportion and cast what one of Europe’s top flu experts calls a “long shadow” over public confidence in vaccines that control potential killers like measles and polio.

“No-one wants to be the next Wakefield,” said Mignot, referring to the now discredited British doctor Andrew Wakefield who sparked a decades-long backlash against the measles, mumps and rubella (MMR) shot with false claims of links to autism.

With the narcolepsy studies, there is no suggestion that the findings are the work of one rogue doctor.

Independent teams of scientists have published peer-reviewed studies from Sweden, Finland and Ireland showing the risk of developing narcolepsy after the 2009-2010 immunization campaign was between seven and 13 times higher for children who had Pandemrix than for their unvaccinated peers.

“We really do want to get to the bottom of this. It’s not in anyone’s interests if there is a safety issue that needs to be addressed,” said GSK’s Begg.

LIFE CHANGED

Emelie’s parents, Charles and Marie Olsson, say she was a top student who loved playing the piano, taking tennis lessons, creating art and having fun with friends. But her life started to change in early 2010, a few months after she had Pandemrix. In the spring of 2010, they noticed she was often tired, needing to sleep when she came home from school.

But it wasn’t until May, when she began collapsing at school, that it became clear something serious was happening.

As well as the life-limiting bouts of daytime sleepiness, narcolepsy brings nightmares, hallucinations, sleep paralysis and episodes of cataplexy – when strong emotions trigger a sudden and dramatic loss of muscle strength.

In Emelie’s case, having fun is the emotional trigger. “I can’t laugh or joke about with my friends any more, because when I do I get cataplexies and collapse,” she said in an interview at her home in the Swedish capital.

Narcolepsy is estimated to affect between 200 and 500 people per million and is a lifelong condition. It has no known cure and scientists don’t really know what causes it. But they do know patients have a deficit of a brain neurotransmitter called orexin, also known as hypocretin, which regulates wakefulness.

Research has found that some people are born with a variant in a gene known as HLA that means they have low hypocretin, making them more susceptible to narcolepsy. Around 25 percent of Europeans are thought to have this genetic vulnerability.

When results of Emelie’s hypocretin test came back in November last year, it showed she had 15 percent of the normal amount, typical of heavy narcolepsy with cataplexy.

The seriousness of her strange new illness has forced her to contemplate life far more than many other young teens: “In the beginning I didn’t really want to live any more, but now I have learned to handle things better,” she said.

TRIGGERS?

Scientists investigating these cases are looking in detail at Pandemrix’s adjuvant, called AS03, for clues.

Some suggest AS03, or maybe its boosting effect, or even the H1N1 flu itself, may have triggered the onset of narcolepsy in those who have the susceptible HLA gene variant.

Angus Nicoll, a flu expert at the European Centre for Disease Prevention and Control (ECDC), says genes may well play a part, but don’t tell the whole story.

“Yes, there’s a genetic predisposition to this condition, but that alone cannot explain these cases,” he said. “There was also something to do with receiving this specific vaccination. Whether it was the vaccine plus the genetic disposition alone or a third factor as well – like another infection – we simply do not know yet.”

GSK is funding a study in Canada, where its adjuvanted vaccine Arepanrix, similar to Pandemrix, was used during the 2009-2010 pandemic. The study won’t be completed until 2014, and some experts fear it may not shed much light since the vaccines were similar but not precisely the same.

It all leaves this investigation with far more questions than answers, and a lot more research ahead.

WAS IT WORTH IT?

In his glass-topped office building overlooking the Maria Magdalena church in Stockholm, Goran Stiernstedt, a doctor turned public health official, has spent many difficult hours going over what happened in his country during the swine flu pandemic, wondering if things should have been different.

“The big question is was it worth it? And retrospectively I have to say it was not,” he told Reuters in an interview.

Being a wealthy country, Sweden was at the front of the queue for pandemic vaccines. It got Pandemrix from GSK almost as soon as it was available, and a nationwide campaign got uptake of the vaccine to 59 percent, meaning around 5 million people got the shot.

Stiernstedt, director for health and social care at the Swedish Association of Local Authorities and Regions, helped coordinate the vaccination campaign across Sweden’s 21 regions.

The World Health Organisation (WHO) says the 2009-2010 pandemic killed 18,500 people, although a study last year said that total might be up to 15 times higher.

While estimates vary, Stiernstedt says Sweden’s mass vaccination saved between 30 and 60 people from swine flu death. Yet since the pandemic ended, more than 200 cases of narcolepsy have been reported in Sweden.

With hindsight, this risk-benefit balance is unacceptable. “This is a medical tragedy,” he said. “Hundreds of young people have had their lives almost destroyed.”

Yet the problem with risk-benefit analyses is that they often look radically different when the world is facing a pandemic with the potential to wipe out millions than they do when it has emerged relatively unscathed from one, like H1N1, which turned out to be much milder than first feared.

David Salisbury, the British government’s director of immunization, says “therein lies the risk, and the difficulty, of working in public health” when a viral emergency hits.

“In the event of a severe pandemic, the risk of death is far higher than the risk of narcolepsy,” he told Reuters. “If we spent longer developing and testing the vaccine on very large numbers of people and waited to see whether any of them developed narcolepsy, much of the population might be dead.”

Pandemrix was authorized by European drug regulators using a so-called “mock-up procedure” that allows a vaccine to be authorized ahead of a possible pandemic using another flu strain. In Pandemrix’s case, the substitute was H5N1 bird flu.

When the WHO declared a pandemic, GSK replaced the mock-up’s strain with the pandemic-causing H1N1 strain to form Pandemrix.

GSK says the final H1N1 version was tested in trials involving around 3,600 patients, including children, adolescents, adults and the elderly, before it was rolled out.

The ECDC’s Nicoll says early warning systems that give a more accurate analysis of a flu strain’s threat are the best way to minimize risks of this kind of tragedy happening in future.

Salisbury agrees, and says progress towards a universal flu vaccine – one that wouldn’t need last-minute changes made when a new strain emerged – would cuts risks further.

“Ideally, we would have a better vaccine that would work against all strains of influenza and we wouldn’t need to worry about this ever again,” he said. “But that’s a long way off.”

With scientists facing years of investigation and research, Emelie just wants to make the best of her life.

She reluctantly accepts that to do so, she needs a cocktail of drugs to try to control the narcolepsy symptoms. The stimulant Ritalin and the sleeping pill Sobril are prescribed for Emelie’s daytime sleepiness and night terrors. Then there’s Prozac to try to stabilize her and limit her cataplexies.

“That’s one of the things that makes me feel most uncomfortable,” she explains. “Before I got this condition I didn’t take any pills, and now I have to take lots – maybe for the rest of my life. It’s not good to take so many medicines, especially when you know they have side effects.”

Delaware Lifts Ban On Mercury in Vaccines

inquisitr.com | Jan 24, 2013

vaccine babyThe nation is in the midst of an epic flu season, and now Delaware is temporarily lifting its ban on a mercury-containing ingredient in vaccinations to keep up with vaccine shortages.

Pediatrician and Director of Public Health Karyl Rattay temporarily changed the state’s flu shot rules this week, lifting the ban on vaccines containing thirmerosal. Thirmerosal is a preservative that contains trace amounts of mercury.

State law generally forbids the use of vaccines containing mercury on pregnant women and children under the age of 8. The law has been in place for years. However, Rattay suggests that thirmerosal has a proven safety record.

“Nonetheless, folks have had concern in the past that there might have been harm,” she said.

The mercury-containing preservative was taken out of vaccines not for substantiated medical reasons, she notes, but because of the heightened perceived connection between autism and vaccines. In a statement, Rattay said that pregnant women and children are particularly vulnerable to the flu, and stated, “Public Health wants to ensure that vaccine is available for those who need it in Delaware,” she said.

Rattay adds that doctors have been concerned at the decreasing availability of the mercury-free vaccine.

“They are not expressing concern about the risk from thimerosal. They are much more concerned about the risk of not being able to protect people from the risk of influenza,” Rattay said.

Nearly 30 children have died from this season’s flu, and two people in Delaware have died from flu-related illness just this month. At this time last year, there were no flu-related deaths reported in the state.

“We branded thimerosal with a scarlet letter,” said Dr. Paul Offit, who heads the Division of Infectious Diseases at The Children’s Hospital of Philadelphia. “And now there are people who are scared of thimerosal even though there is now abundant data showing that the level contained in vaccines was never harmful.”

“The notion that there still are states that have a preference against thimerosal-containing vaccines on their books is outdated, archaic and certainly not supported by the science,” Offit said.

Multiple vaccine doses have resulted in up to 145,000 child deaths in past 20 years

naturalnews.com | Jan 24, 2013

by Jonathan Benson

(NaturalNews) The recommended childhood vaccination schedule has changed dramatically over the years, with children now receiving upwards of 30 vaccines, including multiple combination vaccines, before the age of six. And in many cases, doctors and nurses administer half a dozen or more vaccines all at once during a single visit to make sure children get all these shots and to save time. But according to data compiled from the government’s Vaccine Adverse Events Reporting System (VAERS), as many as 145,000 children or more have died throughout the past 20 years as a result of this multiple vaccine dose approach, and few parents are aware of this shocking fact.

In a study recently published in the journal Human & Experimental Toxicology, researchers evaluated the overall number of hospitalizations and deaths associated with vaccines administered between 1990 and 2010, and compared this data to the number of vaccines given at one time to individual children. Hospitalizations and deaths resulting from one vaccine dose were compared to those of two vaccine doses, in other words, and the same all the way up to eight vaccine doses. Researchers also evaluated overall hospitalization and death rates associated with getting one to four combined vaccine doses, five to eight combined vaccine doses, and one to eight combined vaccine doses.

Upon analysis, the team found that the more vaccines a child receives during a single doctor visit, the more likely he or she is to suffer a severe reaction or even die. According to Heidi Stevenson from Gaia Health, for each additional vaccine a child receives, his or her chance of death increases by an astounding 50 percent — and with each additional vaccine dose, chances of having to be hospitalized for severe complications increase two-fold. To sum it all up, the overall size of the vaccine load was found to be directly associated with hospitalization and death risk, illustrating the incredible dangers of administering multiple vaccines at once.

Parents of children who become injured after just one vaccine tend to cease further vaccinations, suggests data

Interestingly, the total number of reported hospitalizations and deaths from getting just one vaccine was higher than the number reported for getting two, three, or even four vaccines. Though the precise reason for this is unknown, it is believed that newborns mostly fall into the one vaccine category, and those that are injured by a single vaccine tend not to get any more vaccines, hence the immediate decrease observed among children who received only two vaccines. Once a child reaches five vaccinations; however, the hospitalization and death rate jumps dramatically, the reason for which was not investigated as part of the study.

“Our findings show a positive correlation between the number of vaccine doses administered and the percentage of hospitalizations and deaths reports to VAERS,” wrote the authors in their conclusion. “In addition, younger infants were significantly more likely than older infants to be hospitalized or die after receiving vaccines. Since vaccines are administered to millions of infants every year, it is imperative that health authorities have scientific data from synergistic toxicity studies on all combinations of vaccines that infants are likely to receive.”

You can view the complete results of the study in their entirety here: http://gaia-health.com

Toxic mercury ban treaty exempts vaccines for children

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In this April 22, 2012, file photo, Holly Ann Haley, 4, gets vaccinations at the doctor’s office in Berlin, Vt., although the state continues to be embroiled in a debate about continuing to allowing parents to have their children skip the immunizations required for most to attend school. (Associated Press)

The treaty says that certain mercury-added products, such as batteries, lamps, switches, skin-lightening cosmetics, pesticides and thermometers, may not be manufactured, imported or exported no later than 2020.

Mercury-added dental amalgams are also to be phased out.

Treaty on mercury would not affect vaccines with thimerosal

Washington Times | Jan 19, 2013

By Cheryl Wetzstein

A global treaty to reduce toxic mercury in the environment has been completed and will be presented to countries for their agreement to control and reduce ways in which mercury is used, released or emitted.

Negotiations on the Minamata Convention on Mercury, named for the Japanese city that suffered severe mercury poisoning in the 1950s, finished in Switzerland on Saturday.

“Everyone in the world stands to benefit from the decisions take this week in Geneva — in particular, the workers and families of small-scale gold miners, the peoples of the Arctic, and this generation of mothers and babies and the generations to come,” said Achim Steiner, United Nations undersecretary-general and executive director of the United Nations Environment Program, which facilitated the meeting of delegates from 140 member states.

The treaty says that certain mercury-added products, such as batteries, lamps, switches, skin-lightening cosmetics, pesticides and thermometers, may not be manufactured, imported or exported no later than 2020.

Mercury-added dental amalgams are also to be phased out.

However, certain mercury-added products are to be exempted from the ban, including those used for military and civil protection, products with no mercury-free alternative, products used in religious or traditional practices and vaccines containing thimerosal, an ethylmercury preservative.

The omission of thimerosal-containing vaccines from the ban disappointed advocates who believe the preservative plays a role in sickening some children.

“Children’s health took a backseat to special interests. The only major purposeful exposure to mercury that didn’t get addressed was thimerosal,” said Eric Uram, executive director at SafeMinds, which seeks to eradicate autism and other health disorders caused by mercury and man-made toxicants.

However, use of thimerosal vaccines was supported by specialists who advise the World Health Organization, and groups like the American Academy of Pediatrics (AAP).

Fifteen years of research “has failed to yield any evidence of significant harm” — including disorders such as autism — from using thimerosal in vaccines, Dr. Walter Orenstein, associate director of the Emory Vaccine Center at Emory University in Georgia, wrote in AAP’s Dec. 17, 2012, Pediatrics journal.

Millions of children in the developing world depend on multidose vaccines that can be stored without refrigeration; thimerosal prevents bacteria or pathogens from growing in these vaccines, added researchers Katherine King and colleagues in Pediatrics. “Banning thimerosal would amount to banning such multidose vaccines” that currently protect children from tetanus, diphtheria, whooping cough and hepatitis B, they wrote.

The United States uses thimerosal-free vaccines, except in some flu shots, according to the Centers for Disease Control and Prevention.

Mercury is highly toxic to humans and animals when inhaled or ingested, and is particularly harmful to developing brains and nervous systems in children and fetuses.

Global mercury pollution, which will be curtailed under the new treaty, occurs through emissions from mining, power plants, smelters and cement production. Mercury has entered the global food chain, especially via fish and shellfish; shark, swordfish, tilefish and King Mackerel should not be eaten because of their high mercury concentrations, the Food and Drug Administration advises.

The signing of the global mercury ban will occur in October in Minamata, where thousands of Japanese citizens suffered death and injury from eating methylmercury-contaminated seafood from their local waters. It was later discovered that a local chemical factory had released its industrial wastewater into the surrounding waterways.

Guns and drugs: Psychoactive drugs may impact mass shootings

drugs

washingtontimes.com | Jan 15, 2013

byDr. Lind by Peter Lind

OREGON, January 16, 2013 – A few weeks before the Newtown school shooting there was a mall shooting in Oregon. That shooting ended when a civilian pulled out his own gun and drew it on the killer. When the killer saw him, he turned his gun on himself and the ordeal was over. Two dead, seven injured, and over 69 shots fired. Chances are you didn’t hear about this. Chances are you didn’t hear about many shootings that take place across the country.

You may also not have heard that many of the shooters in these cases have a history of taking psychoactive drugs, used to treat a variety of mental illnesses from depression to Schizophrenia.

As American politicians look at gun laws, they cannot ignore the growing observable evidence of prescription medications in the majority of the mass shootings.

The Newtown School shooter reportedly took the pharmaceutical drug Fanapt, made by Novartis Pharmaceuticals Corporation. Fanapt is prescribed to treat schizophrenia in adults, according to the drug company’s literature. Fanapt was approved by the FDA after two short-term research trials: a four week and a six week trial.

Side effects listed in the literature that accompanies Fanapt notes the following: Fanapt can cause “arrhythmia and sudden death – consider using other antipsychotics first.”

Other side effects of Fanapt include suicide, along with hostility, aggression, mania, a confused state, along with problems with impulse control. Fanapt can also cause seizures, erectile dysfunction, high blood pressure, and low blood sugar.

Frequent side effects of Fanapt include restlessness, aggression, and delusion. Fanapt can also cause hostility, paranoia, anorgasmia, confusional state, mania, catatonia, mood swings, panic attack, obsessive-compulsive disorder, bulimia nervosa, delirium, polydipsia psychogenic, impulse-control disorder, and major depression.

Novartis and the FDA state that this drug has not been safely tested on young people. According to Novartis, “Safety and effectiveness in pediatric and adolescent patients have not been established.”

There is evidence that suggests prescription medication may play a role in mass shootings.

Documents show that 109 people have been wounded and 58 killed in recent shootings where the shooters were taking psychotropic drugs. The FDA has reports of 11,000 incidents of violence resulting from these drugs between 2004 -2011, including 300 homicides, representing less than 10% of actual incidents.

Psychology Today, January 5, 2011 describes this problem in detail. Of the 1937 total case reports of violence toward others by individuals taking psychotropic drugs, there were 387 cases of homicide, 404 physical assaults, 27 cases of physical abuse, 896 reports of homicidal ideation, and 223 cases of “violence related symptoms.”

The adverse events reported to the FDA are known to represent but a tiny fraction of all such adverse events. This study simply identified 31 drugs responsible for most of the FDA case reports of violence toward others, with antidepressants near the top of that list.

The many past shootings at school campuses and other public venues should be investigated by government officials concerning whether psychotropic drug use may have been involved in the case.

Moore and his collaborators concluded: “These data provide new evidence that acts of violence towards others are a genuine and serious adverse drug event that is associated with a relatively small group of drugs. Varenicline, which increases the availability of dopamine and serotonin reuptake inhibitors were the most strongly and consistently implicated drugs.”

Selective Serotonin Reuptake Inhibitor (SSRI’s) appear particularly dangerous. SSRI’s raise not only serotonin levels but also potentate the activity of epinephrine, norepinepherine, and in some cases dopamine. These are neuro-active substances that are part of the catecholamine family.

People who use Prozac and other SSRI drugs are five times as likely to commit suicide than if they took no medication at all.

These drugs can cause helplessness, apathy, aggression, and sedation.

Serotonin elevating drugs are prescribed for stress related emotional conditions, yet the evidence is that serotonin is already too high in people suffering from emotional stress. This is because stress liberates free fatty acids from storage, which, in turn, increases the uptake of tryptophan into the brain, increasing the formation of serotonin.

A record of violence has clearly been associated with above average blood serotonin levels.

Politicians, it is time to look at the psychoactive medications use and abuse in America.

Dr Peter Lind practices metabolic and neurologic chiropractic in his wellness clinic in Salem, Oregon. USA. He is the author of 3 books on health, one novel, and hundreds of wellness articles. His clinical specialty is in physical, nutritional, and emotional stress.

 

For more health tips go to http://www.wellnessreport.net

Vaccine Court Awards Millions to Two Children With Autism

“The hatred from the medical community towards families like ours is intense.”

huffingtonpost.com | Jan 14, 2013

by David Kirby

About 1 million children in the United States and about 30 million worldwide have gotten Rotarix vaccine, the FDA says.

The federal Vaccine Injury Compensation Program, better known as “vaccine court,” has just awarded millions of dollars to two children with autism for “pain and suffering” and lifelong care of their injuries, which together could cost tens of millions of dollars.

The government did not admit that vaccines caused autism, at least in one of the children. Both cases were “unpublished,” meaning information is limited, and access to medical records and other exhibits is blocked. Much of the information presented here comes from documents found at the vaccine court website.

Some observers will say the vaccine-induced encephalopathy (brain disease) documented in both children is unrelated to their autism spectrum disorder (ASD). Others will say there is plenty of evidence to suggest otherwise.

What’s more, these cases fit the pattern of other petitions, (i.e., Poling and Banks) in which the court ruled (or the government conceded) that vaccines had caused encephalopathy, which in turn produced permanent injury, including symptoms of autism and ultimately an ASD diagnosis.

And most of these children now have taxpayer dollars earmarked for applied behavioral analysis (ABA), an effective therapy specifically designed to treat ASD.

Meanwhile, parents, grandparents, friends and neighbors of both children testified they were developmentally normal, if not advanced for their age when they developed seizures, spiking fevers and other adverse reactions to their vaccines. According to these eyewitnesses, the children never fully recovered, and instead began losing vocabulary, eye contact and interest in others around them, all classic symptoms of regressive autism.

In the first case, involving a 10-year-old boy from Northern California named Ryan Mojabi, the parents allege that “all the vaccinations” received from 2003-2005, and “more specifically, measles-mumps-rubella (MMR) vaccinations,” caused a “severe and debilitating injury to his brain, described as Autism Spectrum Disorder (‘ASD’).”

The parents, who did not want to be interviewed, specifically asserted that Ryan “suffered a Vaccine Table Injury, namely, an encephalopathy” as a result of his MMR vaccination on December 19, 2003.” (“Table injuries” are known, compensable adverse reactions to immunizations.)

Alternatively, they claim that “as a cumulative result of his receipt of each and every vaccination between March 25, 2003 and February 22, 2005, Ryan has suffered . . . neuroimmunologically mediated dysfunctions in the form of asthma and ASD.”

In vaccine court, the U.S. Department of Health and Human Services acts as the defendant and Justice Department attorneys act as counsel.

In 2009, Ryan’s case was transferred to vaccine court’s Autism Omnibus Proceedings, according to the docket. A year-and-a-half later, the government conceded that MMR vaccine had indeed caused Ryan’s encephalopathy.

HHS agreed that “Ryan suffered a Table injury under the Vaccine Act — namely, an encephalitis within five to fifteen days following receipt,” of MMR, records show. “This case is appropriate for compensation.”

Whether HHS agreed with Ryan’s parents that his vaccine-induced brain disease led to ASD is unknown. The concession document is under seal.

In December 2003, when Ryan was nearly two, he received his first MMR and hepatitis B vaccines before his family left for an extended trip overseas. That day, his mother testified, Ryan began shaking with uncontrollable tremors and “was really uncomfortable, he didn’t feel well at all.”

The nurse at Ryan’s pediatrician said the symptoms were “pretty normal after the vaccination,” and advised Tylenol. The next day, Ryan began crying, “but it’s not a normal crying,” his mother testified. “He didn’t go to sleep, he was without energy.”

The family considered postponing their holiday, but that wasn’t feasible. The doctor’s office said it was fine to travel. Prior to leaving, Ryan’s mother said, the boy had difficulty breathing and “was without energy and sleepy.” He could no longer hold his head up, something “he could do prior to the vaccinations.” At the airport, Ryan began “screaming,” she recalled. “He was just opening and closing his eyes so hard, he was pulling my hair.”

After his shots, she added, Ryan “stopped saying those words that he had, even mommy and daddy, that he had repeated a hundred times before.”

In early January, while still abroad, Ryan was rushed to the hospital with vomiting, high fever and red spots covering his body “from head to toe in a measles-like rash,” the attending physician said. Ryan was diagnosed with “febrile convulsion, probably related to MMR.”

The next day, another doctor diagnosed him with “high fever, skin rash, tremors, and lethargy,” which were “most likely due to an adverse reaction to multiple vaccines he received earlier.”

Two days later, Ryan returned to the hospital with a persistent fever of 104 or more.

Ryan’s parents testified that, upon returning home, they expressed worry to their pediatrician about behavioral problems, non-responsiveness and language loss, which later produced an ASD diagnosis.

At trial, however, the government argued powerfully that written medical records, and the recollections of Ryan’s doctor, were inconsistent with his parents’ testimony. If Ryan had truly suffered an MMR encephalopathy, for example, his family would never have taken him overseas. And his parents’ complaints of ASD symptoms were raised a full year after returning from abroad, they alleged. It looked like the family had a weak case.

But then something changed.

In October, 2010, Ryan’s attorney filed four new exhibits (under seal) and proposed amending the court’s “findings of fact.” In January and May of 2011, several more exhibits were filed, along with a motion to further supplement the findings of fact.

A month later HHS conceded the case, which moved into the damages phase.

Award details were announced a few days ago: A lump sum of $969,474.91, to cover “lost future earnings ($648,132.74), pain and suffering ($202,040.17), and life care expenses for Year One ($119,302.00),” plus $20,000 for past expenses.

Another undisclosed sum, several millions more, will be invested in annuities to cover yearly costs for life, which could total $10 million or more, not accounting for inflation. Nearly $80,000 was earmarked for ABA in the first two years.

The second case involves a girl named Emily, whose mother, Jillian Moller, filed back in 2003 and has been fighting in vaccine court since. The docket, crammed with 188 items, documents Moller’s extended but victorious struggle to win compensation for Emily, who has seizure disorder and PDD-NOS, a form of ASD.

Moller alleged that Emily was severely injured by a reaction to the DTaP vaccine at 15 months (when MMR, HiB and Prevnar were also given). “She had a vaccine reaction and she just spiraled out of control,” Moller said in an interview.

Emily’s fever spiked to 105.7 and she began screaming. She stared blankly and developed seizures. Before long she began “shaking episodes” at night and “repetitive behaviors, including arm flapping and spinning,” court documents show. Like Ryan, she developed a measles-type rash.

Things went from bad to worse. Emily’s medical record is filled with damage and suffering. One neurologist, for example, noted that Emily “had staring spells and an abnormal EEG.” Another diagnosed “encephalopathy characterized by speech delay and probable global developmental delay that occurred in the setting of temporal association with immunizations as an acute encephalopathy.”

Moller filed for an encephalopathy Table injury in 2003, unaware her daughter would be diagnosed with ASD.

Two hearings were held in 2005. “I was badgered and harassed for four hours on the stand,” she said. “They said Emily couldn’t have been that sick, or else I would’ve taken her to the ER. But I took her to my doctor and he said not to bring her to the hospital!”

Government lawyers insisted that Emily had suffered neither a vaccine injury nor encephalopathy. But every alternative cause they suggested “made no sense, because she showed no signs of those things before that vaccination,” Moller said.

The case dragged on for years, with motions and counter-motions, status reports and expert medical reports. In 2007, Moller filed for summary judgment. That also took years, as more medical records were submitted to bolster Emily’s case.

After the ASD diagnosis, the judge reportedly became convinced that Emily would prevail. “My attorney said she was angry, she felt forced into a corner with no choice but to find for us,” Moller said. “She said, ‘Emily has autism, and I don’t want to give other families who filed autism claims any hope.'”

The government agreed to settle. Last spring the case went into mediation and, on December 3 HHS made its proffer, which was entered into the record on the 28th. Emily was awarded a lump sum of $1,030,314.22 “for lost future earnings ($739,989.57), pain and suffering ($170,499.77) and life care expenses for Year One ($119,874.88) plus $190,165.40 for past expenses.” Some of that money will go to ABA therapy.

Based on the first year payout, another estimated $9 million will buy annuities for annual expenses through life, which after inflation has the potential to pay over $50 million dollars.

HHS did not admit that vaccination caused encephalopathy or autism, but merely decided not to dedicate more resources to defending the case.

“I don’t understand why they fought so hard,” Moller said. “We had the evidence: the EEG, the MRI, everything was consistent with encephalopathy, post-vaccination. How can government attorneys claim what our doctors said happened, didn’t happen?”

Perhaps the feds were loath to concede yet another vaccine case involving autism. Four cases in the Autism Omnibus Proceedings were recently compensated. Three of those cases are marked with asterisks, indicating the government did not conclude that autism can be caused by vaccines. But the fourth autism case that was paid out in 2013 (Ryan’s case? We don’t know) has no such caveat.

As for Emily, she is “not too good,” Moller said. “Her emotional state is fragile, at best. She has seizure problems and autoimmune issues… And it’s a constant fight when you have a vaccine-injured child. It’s not just the disability, it’s the ignorance. The hatred from the medical community towards families like ours is intense.”

Meanwhile, as HHS says it “has never concluded in any case that autism was caused by vaccination,” it is still underwriting autism treatments such as ABA for children in its vaccine-injury program.

Warning: Most Flu Shots Contain Mercury

flu shot contains mercury

ecochildsplay.com | Jan 14, 2013

by Jennifer Lance

The flu has been getting a lot of media attention lately, as emergency rooms are filled with sick patients and pharmacies are running out of the flu vaccine.

There are two reasons NOT to get the flu vaccine:

1. Each year the flu vaccine is actually developed based on what researchers think will be prevalent.
WebMD explains:

Each year, the flu vaccine contains several different kinds of the virus. The strains chosen are the ones that researchers say are most likely to show up that year.

The mainstream media has featured many ill individuals who did receive the flu vaccination but are still very sick. Apparently, they were not protected from the strain that is prevalent currently.

2. Most flu shots contain mercury.
Mercury in the form of thimerosal is used as a preservative in most flu shots. This is the same thimerosal that was removed from childhood vaccines in the United States that has caused autism like symptoms in primates, even though the medical community does not support is correlation. Regardless scientific proof of autism and other potential negative side effects, mercury was removed from childhood vaccines in 2001. The CDC explains:

2001
Except for influenza (flu), thimerosal is removed from or reduced in all vaccines routinely recommended for children 6 years of age and under manufactured for the U.S. market.

October 1. IOM’s Immunization Safety Review Committee issues a report concluding there is not enough evidence to disprove claims that thimerosal in childhood vaccines causes autism, attention deficit hypersensitivity disorder, or speech or language delay.

May 5. A risk assessment of thimerosal use in childhood vaccines finds no evidence of harm from the use of thimerosal as a preservative, other than redness and swelling at the injection site…

2004
May 28. ACIP recommends that children between the ages of 6 and 23 months routinely receive an inactivated influenza (flu) vaccine. ACIP does not recommend using the thimerosal-free flu vaccine over the thimerosal-containing flu vaccine, and states that the benefits of flu vaccination outweigh any risk from thimerosal exposure.

 

There are four types of flu vaccine, and most of them contain thimerosal.  Again, we refer to the CDC:

Do the 2012-2013 seasonal flu vaccines contain thimerosal?

The Food and Drug Administration (FDA) has approved several formulations of the seasonal flu vaccine, including multi-dose vials and single-dose units. (See Table of Approved Influenza Vaccines for the U.S. 2012–2013 Season.) Since seasonal influenza vaccine is produced in large quantities for annual immunization campaigns, some of the vaccine is produced in multi-dose vials, and contains thimerosal to safeguard against possible contamination of the vial once it is opened.

The single-dose units are made without thimerosal as a preservative because they are intended to be opened and used only once. Additionally, the live-attenuated version of the vaccine (the nasal spray vaccine), is produced in single-dose units and does not contain thimerosal.

It is possible to receive the flu vaccine without mercury, and it is always good advice to speak with your doctor, rather than rely on a blog such as this, for medical advice.  Personally, I would rather take my chances with the flu than be exposed to chemicals, such as mercury, as well as gamble on the effectiveness of the vaccine. That being said, people do die from the flu.  Typically, they are very young or very old or have a compromised immune system from another illness.  A healthy person will suffer from the flu, but they will survive.

Furthermore, many people experience flu like symptoms after receiving the flu vaccine.

I am on the tail end of the flu.  It has lasted for two weeks!  I don’t think it is the same strain featured on the news, as my fever has not been super high, but I have been suffering.

I have never had a flu shot.  Of my friends and family that do get vaccinated, they still get sick just as much as my family.

If you want to protect your family from the flu, the best natural methods are:

  1. Get plenty of rest
  2. Stay hydrated
  3. Eat whole foods (7-10 servings organic fruit and vegetables)
  4. Plenty of Vitamin D!
  5. Wash your hands!