Aftermath News

Entries categorized as ‘Medical Mafia’

FDA weighs approval of adult psychiatric drugs for children

June 6, 2009 · Leave a Comment

Officials have concerns about exposing younger patients to the drugs’ side effects.

AP | Jun 5, 2009

By MATTHEW PERRONE

WASHINGTON (AP) — Three blockbuster psychiatric drugs currently approved for adults also appear to work in adolescents, though federal health officials have concerns about exposing younger patients to the drugs’ side effects.

The Food and Drug Administration is reviewing drugs from AstraZeneca PLC, Eli Lilly & Co. and Pfizer Inc. for use in patients between the ages of 10 and 17. The drugs — already approved to treat schizophrenia and bipolar mania in adults — had combined sales of more than $7.4 billion last year, according to IMS Health.

FDA reviewers on Friday said they were wary of exposing youngsters to the drugs’ side effects, including weight gain and high blood sugar, “because they may be exposed for many decades.”

“These risks are of particular concern in pediatric patients because of the lifelong nature of these disorders,” FDA director for psychiatric products, Dr. Thomas Laughren, wrote in documents posted online.

The FDA released its review of the drugs ahead of a meeting Tuesday where outside experts will weigh in on the drugs’ risks and benefits. The agency is not required to follow the group’s advice, though it usually does.

Many doctors already prescribe the medications to children and adolescents, although regulators have not officially cleared that use. Physicians are free to prescribe medicines as they see fit, though companies can only promote them for FDA-approved indications.

AstraZeneca and Lilly are seeking permission to market their drugs for adolescents with schizophrenia and bipolar mania, also called manic depressive disorder. Pfizer is seeking a pediatric bipolar disorder indication for its drug.

FDA drug reviewers noted that the “safety profile of the pediatric population is very similar compared to that of the adult population.” And while there were no side effects unique to younger patients, there were differences in the frequency of the effects compared with adults.

In schizophrenia studies of Lilly’s Zyprexa, more than 30 percent of adolescents gained weight, compared with just 6 percent of adults. On average, adolescents gained nearly 10 pounds, compared with 6 pounds for adults.

Lilly is seeking FDA approval to market the drug as a second-line treatment, or a second option after other drugs have been tried.

Adolescent patients taking Pfizer’s Geodon were more likely to report sleepiness and dystonia, a movement disorder that causes muscle spasms. AstraZeneca noted higher rates of increased appetite and blood pressure among children and adolescents taking Seroquel compared with adults.

Despite concerns over the side effects, Laughren and other FDA officials acknowledged the need for additional drugs to treat schizophrenia and bipolar disorder in teenagers and older children.

“Schizophrenia and bipolar disorder are serious illnesses in pediatric patients and represent substantial burden for both patients and their families,” Laughren said.

Currently only two drugs are cleared for those uses: Bristol-Myers Squibb’s Abilify and Johnson & Johnson’s Risperdal. Abilify was the second best-selling anti-psychotic drug in the U.S. last year with sales of $3 billion. Risperdal was fourth with $1.6 billion in sales.

Schizophrenia affects about 2.4 million Americans and is characterized by hallucinations, delusions and social withdrawal, according to the National Institute of Mental Health. About 5.7 million Americans experience bipolar disorder, which causes rapid mood swings and shifts in energy.

Categories: Big Pharma · Child Takeover · Eugenics · Health & Fitness · Medical Mafia · Mental Health

U.S. military: Heavily medicated and armed

May 29, 2009 · Leave a Comment

Prescription pill dependency among American troops is on the rise

MSNBC | May 19, 2009

U.S. military: Heavily armed and medicated

By Melody Petersen

Marine Corporal Michael Cataldi woke as he heard the truck rumble past.

He opened his eyes, but saw nothing. It was the middle of the night, and he was facedown in the sands of western Iraq. His loaded M16 was pinned beneath him.

Cataldi had no idea how he’d gotten to where he now lay, some 200 meters from the dilapidated building where his buddies slept. But he suspected what had caused this nightmare: His Klonopin prescription had run out.

His ordeal was not all that remarkable for a person on that anti-anxiety medication. In the lengthy labeling that accompanies each prescription, Klonopin users are warned against abruptly stopping the medicine, since doing so can cause psychosis, hallucinations, and other symptoms. What makes Cataldi’s story extraordinary is that he was a U. S. Marine at war, and that the drug’s adverse effects endangered lives — his own, his fellow Marines’, and the lives of any civilians unfortunate enough to cross his path.

“It put everyone within rifle distance at risk,” he says.

In deploying an all-volunteer army to fight two ongoing wars, in Iraq and Afghanistan, the Pentagon has increasingly relied on prescription drugs to keep its warriors on the front lines. In recent years, the number of military prescriptions for antidepressants, sleeping pills, and painkillers has risen as soldiers come home with battered bodies and troubled minds. And many of those service members are then sent back to war theaters in distant lands with bottles of medication to fortify them.

According to data from a U. S. Army mental-health survey released last year, about 12 percent of soldiers in Iraq and 15 percent of those in Afghanistan reported taking antidepressants, anti-anxiety medications, or sleeping pills. Prescriptions for painkillers have also skyrocketed. Data from the Department of Defense last fall showed that as of September 2007, prescriptions for narcotics for active-duty troops had risen to almost 50,000 a month, compared with about 33,000 a month in October 2003, not long after the Iraq war began.

In other words, thousands of American fighters armed with the latest killing technology are taking prescription drugs that the Federal Aviation Administration considers too dangerous for commercial pilots.

Military officials say they believe many medications can be safely used on the battlefield. They say they have policies to ensure that drugs they consider inappropriate for soldiers on the front lines are rarely used. And they say they are not using the drugs in order to send unstable warriors back to war.

Yet the experience of soldiers and Marines like Cataldi show the dangers of drugging our warriors. It also worries some physicians and veterans’ advocates. “There are risks in putting people back to battle with medicines in their bodies,” says psychiatrist Judith Broder, M. D., founder of the Soldiers Project, a group that helps service members suffering from mental illness.

Prescription drugs can help patients, Dr. Broder says, but they can also cause drowsiness and impair judgment. Those side effects can be dealt with by patients who are at home, she says, but they can put active-duty soldiers in great danger. She worries that some soldiers are being medicated and then sent back to fight before they’re ready.

“The military is under great pressure to have enough people ready for combat,” she says. “I don’t think they’re as cautious as they would be if they weren’t under this kind of pressure.”

Brought more than memories back

When Cataldi talks about what happened to him in Iraq, he begins with an in incident that took place on a cold January night in 2005, when he and five other Marines received a radio call informing them that a helicopter had disappeared. The men roared across the desert of western Iraq and found what was left of the chopper. Flames roared from the pile of metal. Cataldi, 20, was ordered to do a body count.

The pilot’s body was still on fire, so he shoveled dirt on it to douse the acrid flames. He picked up a man’s left boot in order to find the dog tag every Marine keeps there. A foot fell to the ground. “People were missing heads,” Cataldi remembers. “They were wearing the same uniform I was wearing.”

The final death toll from that crash of a CH-53E Super Stallion was 30 Marines and one sailor.

For days, Cataldi couldn’t escape the odor of burning flesh. “I had the smell all over my equipment,” he says. “I couldn’t get it off .”

When he returned to his stateside base at Twentynine Palms, California, he knew he’d brought more than memories back from Iraq. He would cry for no reason. He flew into fits of rage. One night he woke up with his hands around the throat of his wife, Monica, choking her.

“It scared the crap out of me,” he says.

He went to see a psychiatrist on base. “He said, ‘Here’s some medication,’ ” Cataldi recalls. The prescribed drugs were Klonopin, for anxiety; Zoloft, for depression; and Ambien, to help him sleep.

Later, other military doctors added narcotic painkillers for the excruciating pain in his leg, which he’d injured during a training exercise. He was also self-medicating with heavy doses of alcohol.
Those prescriptions didn’t stop the Marine Corps from sending Cataldi back to Iraq. In 2006, he returned to the same part of the Iraqi desert to do the same job: performing maintenance on armored personnel carriers known as LAVs. He also took his turn driving the 14-ton tanklike vehicles, one of which was armed with a 25 mm cannon and two machine guns and loaded with more than 1,000 rounds of ammunition.

Marine Major Carl B. Redding says he can’t talk about the medical history of any Marine because of privacy laws. He says the Corps has procedures to ensure that service members taking medications for psychiatric conditions are deployed only if their symptoms are in remission. Those Marines, he says, must be able to meet the demands of a mission.

But it’s difficult to square those regulations with Cataldi’s experience. His medications came with written warnings about the dangers of driving and operating heavy machinery. The labels don’t lie.

One night, Cataldi took his pills after his commander told him he was done for the day. Five minutes later, however, plans changed, and he was told to drive the LAV. He asked the Marine sitting behind him to help keep him awake. “I said, ‘Kick the back of my seat every 5 minutes,’ and that’s what he did.”

Cataldi says he managed on the medications — until his Klonopin ran out. The medical officer told him there was no Klonopin anywhere in Iraq. So the officer gave him a drug called Seroquel. That’s when Cataldi says he started to become “loopy.”

“I’d go to pick up a wrench and come back with a hammer,” he says. “I wasn’t able to do my job. I wasn’t able to fight.”

Soldiers on medication

Soldiers have doped up in order to sustain combat since ancient times. Often their chosen drug was alcohol. And Iraq isn’t the first place U. S. military doctors have prescribed medications to troops on the front. During the Vietnam war, military psychiatrists spoke enthusiastically about some newly psychiatric medicines, including Thorazine, an anti-psychotic, and Valium, for anxiety. According to an army textbook, doctors frequently prescribed those drugs to soldiers with psychiatric symptoms. Anxiety-ridden soldiers with upset bowels were sometimes given the antidiarrheal Compazine, a potent tranquilizer.

But the use of those drugs in Vietnam became controversial. Critics said it was dangerous to give soldiers medications that slowed their reflexes, a side effect that could raise their risk of being injured, captured, or killed. That risk was real. In a report supported by the U. S. Navy 14 years after the United States withdrew from Vietnam, researchers looked at the records of all Marines wounded there between 1965 and 1972. Marines who’d been hospitalized for psychiatric reasons before being sent back to battle were more likely to have been injured in combat than those who hadn’t been hospitalized.

Critics of medication use in Vietnam also said that a soldier traumatized by battle may not be coherent enough to give his consent to take the drugs in the first place. Plus, a soldier would risk court-martial if he refused to follow orders, they said, making it unlikely he could make a reasoned decision about taking the medications.

After the war, the practice of liberally giving psychiatric drugs to warriors fell out of favor. In War Psychiatry, a 1995 military medical textbook, a U. S. Air Force flight surgeon warned about the use of psychiatric drugs, saying they should be used sparingly.

“Sending a person back to combat duty still under the influence of psychoactive drugs may be dangerous,” he wrote. “Even in peacetime, people in the many combat-support positions… would not be allowed to take such medications and continue to work in their sensitive, demanding jobs.”

Colonel Elspeth Cameron Ritchie, M. D., M. P. H., a psychiatrist and the medical director of the strategic communication directorate in the Office of the Army Surgeon General, acknowledges that writing more prescriptions for frontline troops was a change in direction for the Pentagon. “Twenty years ago,” she says, “we weren’t deploying soldiers on medications.”

Today it’s not uncommon for a soldier to arrive in Iraq while taking a host of prescription drugs. The Pentagon explained its new practice in late 2006, stating that there are “few medications that are inherently disqualifying for deployment.”

According to Colonel Ritchie, military officials have concluded that many medicines introduced since the Vietnam War can be used safely on the front lines. Military physicians consider antidepressants and sleeping pills to be especially helpful, she says. Doctors have also found that small doses of Seroquel, an anti-psychotic, can help treat nightmares, she says, even though the drug is not approved for that use.

Full Story

Categories: Big Pharma · Medical Mafia · Mental Health · Militarization · Mind Control · Perpetual War · Social Engineering

After suicide of 7-year-old, agency finds serious shortcomings in monitoring of foster children on psychotropic drugs

May 29, 2009 · Leave a Comment

Review finds shortfalls in monitoring of foster children on psychiatric drugs

13.19 percent, are taking one or more psychotropic medications

St. Petersburg Times | May 29, 2009

By Kris Hundley

Spurred by the shocking suicide of a 7-year-old on psychiatric drugs, the agency in charge of Florida’s foster children has discovered serious shortcomings in its monitoring of kids on such powerful prescriptions.

After reviewing its files, the Department of Children and Families determined it had undercounted the number of foster kids on such medications as Risperdal and Adderall, overlooking hundreds of cases.

It also has failed to meet its legal requirement that such prescriptions be given only after parental consent or court order.

On Thursday, DCF said a review of the files of more than 20,000 children currently in the state’s foster care showed 2,669, or 13.19 percent, are taking one or more psychotropic medications.

That compares with about 4 or 5 percent of children in the general population who are on such prescriptions.

Of those foster children taking drugs, DCF discovered 16 percent had no proof either a parent or judge had signed off on the prescription, as required by a 2005 Florida law.

“That is unacceptable,” said DCF Secretary George Sheldon. “We’re going to bring every single case of a foster child on drugs into compliance with the law.”

Concerns about pediatric use of antipsychotic and antidepressants such as Adderall and Risperdal have been growing along with increased warnings of such side effects as suicide, diabetes and weight gain. Few of the drugs have been tested or approved by the FDA for children, though physicians can prescribe them for this age group.

Robin Rosenberg, a Tampa lawyer and deputy director of Florida’s Children First, said advocacy groups like hers have been fighting for oversight of psychotropic drugs for years. “We’re not as far along as we should have been if the state had followed up on serious concerns starting in the late 1990s,” she said. “It’s a shame we’re in this place today.”

Sheldon, who was named to the top job at DCF in October, left no doubt that he had been deeply affected by Gabriel Myers, the 7-year-old who hanged himself on a shower hose in South Florida in mid April. The boy was in his third foster home and on Vyvanse, a medication for ADHD, as well as Symbyax, a combination antipsychotic and antidepressant.

Though his caseworker repeatedly said Gabriel’s mother had agreed to the medications, that was not true. The boy’s psychotropic medications also had not been entered in the state’s tracking system.

To correct ongoing problems, Sheldon set a deadline of June 5 for action on cases without consent. This could include scheduling new doctors’ appointments, gaining informed consent from parents or expediting a judge’s review of the prescription.

Sheldon said he also was going to focus on the cases of 73 children under age 6 found to be on psychotropic drugs.

“I want a sense of urgency, but I also want to get it right,” he said. “I want to move forward, but I think it’s important for the agency to apologize for misinformation it may have put out in the past.”

Flaws in DCF’s record-keeping became clear in the immediate aftermath of Gabriel’s death. An initial review of the state’s database showed only 1,950 kids on psychotropic prescriptions. After a thorough review of individual records, however, that number grew by more than 700.

Preliminary data released in mid May also showed some questionable dates on judicial consent. Though it’s not inconceivable a judge might sign an order on a Saturday or Sunday, early returns showed weekend consent orders on 129 occasions.

The final database, including information on types of drugs and diagnoses, was not available Thursday. Sheldon said a summary of the drug data would be posted on the DCF Web site and updated weekly.

“I’ve got a lot more confidence in these numbers than I had two weeks ago,” he said. “But any database is only as good as the quality of the information being put into it.”

One ongoing area of concern, Sheldon said, is the validity of any consent given by parents whose kids are in the state’s custody.

“A parent whose child is taken into our care is going to sign virtually anything and that’s not informed consent,” he said. “My preference is that the biological parent have a dialogue with the psychiatrist.”

Now that DCF has a handle on the number of foster children on psychotropic drugs, Sheldon said the department can begin to address the bigger issue of the efficacy of such drugs.

He has asked an independent panel investigating Gabriel Myers’ death to make recommendations on improving DCF’s oversight of these medications. Sheldon said a second-party review of all such prescriptions might be necessary; currently, only prescriptions for kids under age 6 require such review.

DCF has set up a page on its Web site that tracks the progress of the panel investigation into the boy’s suicide. The page includes a photo of the smiling boy.

“We have his face on the screen watching us to see how well we learned from his life and death,” Sheldon said. “We cannot let him down.”

Categories: Big Pharma · Child Takeover · Crime & Corruption · Eugenics · Family Breakdown · Health & Fitness · Medical Mafia · Mental Health · Mind Control · Social Degeneration · Social Engineering

Nanotechnology allows vaccines to be forced through the skin without needles

May 28, 2009 · 1 Comment

nanoparticle_vaccination

High-frequency sound waves interact with an emulsion containing polymer, medicament, and fluorescent dye to form spherical nanoparticles, which are then harvested, charged, and applied to foil-backed film. After applying this film to the skin, a pulsed electric field opens pores and drives nanoparticles toward the waiting dendritic cells. Diagrams courtesy of Mark Horenstein and David Sherr.

Hate Needles? No Problem

New pulse-patch system could make vaccines cheap, fast, and easy

BU Today | May 27, 2009

By Mark Dwortzan

For all the advances of modern medicine, today’s drug and vaccine delivery methods still have their drawbacks: hypodermic needles, medicated patches, and ultrasonic methods may offer a range of options, but all lack speed and precision.

Plus, there’s another fact of life: needles can hurt.

Since the dawn of modern medicine — well, maybe since the days of Star Trek — doctors and patients have wished for an easy, injection-free option, a device that goes on your arm, and zap, you’re done.

Now a team of Boston University researchers is developing just that: an electrostatic nano-pulse method for rapidly delivering vaccines and drugs through the skin. Funded in its pilot stage by BU’s Center for Integration of Medicine & Innovative Technology, the team aims to develop a clinical device with widespread applications, including low-cost inoculation in developing countries and rapid antidote dispersal in the event of an epidemic.

Conceived by principal investigators Mark Horenstein, a College of Engineering professor of electrical and computer engineering, and David Sherr, a School of Public Health professor of environmental health, the idea is to put a drug or vaccine inside a biodegradable nanoparticle as small as a human pore. Then, an electrostatic voltage pulse drives it through the skin, where dendritic cells transport it to lymph nodes and generate the immune system’s response.

Sherr has developed plans to evaluate the nano-pulse method in laboratory mice by tracking fluorescent nanoparticles and adjusting the pulse strength. “If we can get the nanoparticles at about one-fifth the depth of a typical human hair and into a layer of skin called stratum corneum,” he says, “that layer has a direct line to the lymph node system.” The team will soon embark on a six-month pilot study to test the concept.

A key challenge is the electric current needed for delivery.

Horenstein is trying to design a device that will drive nanoparticles (seen through a scanning electron microscope, left; fluorescent dye, shown under UV light, helps track the nanoparticles’ movement, right) into the skin with fewer than 50 volts of electricity, the maximum level thought safe for humans. “Usually when you’re trying to drive particles with this level of force, you need thousands of volts,” Horenstein says. “So it all comes down to designing the right methods and structures.”

Categories: Big Pharma · Medical Mafia · Propaganda

ADHD treatment causes young boys to develop female breasts

May 27, 2009 · 2 Comments

3news.co.nz | May 26, 2009

In Janssen's own clinical trials, 43 children developed the abnormal breasts

In Janssen's own clinical trials, 43 children developed the abnormal breasts

A drug used to treat ADHD children is causing concern in the United States.

It is called Risperdal and it is supposed to be used primarily for adults with sever psychological problems.

But last year it was prescribed more than 6.5 million times.

The side effects include young males developing female sex organs.

Nineteen-year-old John was just seven when he began taking Risperdal for ADD.

Even though the FDA approved the drug only for adult patients who were psychotic, John’s doctor and others widely prescribed it to kids for less severe behaviour problems.

Once taking Risperdal, John’s mum says he became aggressive, sleepy, and developed bowel problems. But the biggest shock came when he was 14 and started developing women’s breasts.

“He asked me if he was a girl,” she says.

It turns out Risperdal can increase production of a hormone called prolactin, which stimulates breast growth. It is called gynecomastia – and it is irreversible.

Risperdal and other so-called “atypical anti-psychotics” have exploded in use.

Hundreds of thousands of kids have been prescribed Risperdal in the 14 years it has been on sale – long before the FDA approved it for very limited pediatric use in 2006.

John and most of the other children were not psychotic at all, but were given Risperdal for behaviour disorders including autism and ADD.

Attorney Stephen Sheller is suing Janssen, which makes Risperdal. He claims Janssen marketed Risperdal for unapproved uses in children, downplayed serious risks like diabetes and seizures.

Janssen would not agree to an interview but told us the breast growth risk is “clearly stated in the FDA-approved” labelling, and “we only promote our products for their FDA-approved indications.”

Nobody knows how often it happens. But in Janssen’s own clinical trials with fewer than 2,000 children (1,885), 43 developed the abnormal breasts.

Mr Sheller represents John and nine other boys – one of whom was only four when he developed a breast on one side and began producing milk.

The treatment for the unbridled breast growth is as unthinkable as the disorder: painful removal of the breasts.
Eventually, the boys can appear normal again.

The family’s lawsuit is still in court.

But John’s mother says surgery did not fix all of the problems from the medicine.

When asked if John still thinks he’s a girl his mother wells up and cries before answering, “yes.”

As for Risperdal – it’s still on the market.  And families say putting even more children at risk.

Categories: Big Pharma · Child Takeover · Cover-ups · Crime & Corruption · Eugenics · Feminism · Health & Fitness · Medical Mafia · Mental Health · Mind Control · Sexual Agendas · Social Engineering

Children who have flu jab ‘three times more likely to need hospital care’

May 26, 2009 · Leave a Comment

“Diet, injections, and injunctions will combine, from a very early age, to produce the sort of character and the sort of beliefs that the authorities consider desirable, and any serious criticism of the powers that be will become psychologically impossible.”

- Bertrand Russell, “The Impact of Science on Society”, 1953, pg 49-50

WDDTY | May 20, 2009

Children who have the standard flu jab are three times more likely to end up in hospital. The vaccine is also useless at preventing the disease, new research has discovered.

Children with asthma are especially vulnerable after being given the annual flu vaccine, TIV (trivalent inactivated flu vaccine). Children aged from six months to 18 years are recommended to have the vaccine each year.

Researchers from the Mayo Clinic in Rochester made the discovery after studying 263 children who had had flu, and whether or not they had been vaccinated.

They discovered that children who had been vaccinated were three times more likely to need hospital care than those not vaccinated, and the risk was even higher in children who had asthma.

It was also clear that the vaccine had not protected the children against flu, the researchers told a conference this week.

(Source: 105th International Conference of the American Thoracic Society in San Diego).

Categories: Big Pharma · Bioweapons · Child Takeover · Depopulation · Eugenics · Health & Fitness · Medical Mafia

Aerosol delivery of drugs via nanoparticles to increase patient compliance

May 22, 2009 · 3 Comments

Aerosol Delivery of Antibiotics via Nanoparticles Provide a Means to Improve Drug Delivery

AZoNano | May 19, 2009

Aerosol delivery of antibiotics via nanoparticles may provide a means to improve drug delivery and increase patient compliance, thus reducing the severity of individual illnesses, the spread of epidemics, and possibly even retarding antibiotic resistance.

Delivery of antibiotics via nanoparticles has shown promise as a drug delivery mechanism, particularly for controlled release or depot delivery of drugs to decrease the number of doses required to achieve a clinical effect. The effectiveness of this delivery mechanism has not been confirmed directly either in infection models or in patients, but according to new data to be presented on Tuesday, May 19, at the American Thoracic Society’s 105th International Conference in San Diego, this delivery technique appears indeed promising.

Carolyn L. Cannon, M.D., Ph.D. from Washington University School of Medicine, and colleagues from the Center for Silver Therapeutics Research at the University of Akron in OH investigated the efficacy of nanoparticle-encapsulated silver-based antibiotics for treating pulmonary infections in a mouse model of pneumonia. Treatment with antibiotic-laden nanoparticles effectively eliminated respiratory infections in mice that had been inoculated with Pseudomona aeroginosa, a common bacterial species that often infects the respiratory tract in humans, particularly immunocompromised patients, ventilated patients or those with cystic fibrosis.

Infected mice that inhaled aerosolized nanoparticles encapsulating silver carbene complexes (SCCs), a novel class of silver-based antimicrobials with broad-spectrum activity, showed a significant survival advantage over the control mice that received nanoparticles without the SCCs. Treated mice also had decreased lung bacterial burden and spread, compared to the control mice. Moreover, the treatment with nanoparticles occurred once every 24 hours, a regimen that is known to increase compliance in human patients, versus the usual dosing interval of inhaled antibiotics for P. aeruginosa, which is twice daily.

“We were surprised and thrilled to see a 100 percent survival advantage in mice treated daily with SCC22-loaded nanoparticles at doses significantly lower than those used to achieve a similar survival advantage in twice-daily dosing of unencapsulated SCC22. During a 72 hour period, all of the infected control mice died, whereas all of the mice that received just two doses of SCC22-loaded nanoparticles spaced 24 hours apart survived.”

“My collaborators, Wiley Youngs, Ph.D., and Yang Yun, Ph.D., and I are eager to complete toxicity studies that would enable us to start clinical trials,” said Dr. Cannon. “While the mouse studies are tantalizing, the goal that propels our research is realizing the promise of these novel antibiotics and delivery mechanisms through an analogous survival advantage in patients.”

Categories: Big Pharma · Bioweapons · Medical Mafia

Teen forced into chemo

May 18, 2009 · Leave a Comment

Straits Times | May 16, 2009

Daniel was diagnosed with Hodgkin's lymphoma in January. - PHOTO: AP

Daniel was diagnosed with Hodgkin's lymphoma in January. - PHOTO: AP

MINNEAPOLIS – A MINNESOTA couple who refused chemotherapy for their 13-year-old son on religious grounds were ordered on Friday to have the boy re-evaluated to see if he would still benefit from the cancer treatment – or if it may already be too late.

Brown County District Judge John Rodenberg found Daniel Hauser has been ‘medically neglected’ by his parents, Colleen and Anthony Hauser.

The judge allowed Daniel to stay with his parents, noting they love him and acted in good faith. But he gave them until Tuesday to get an updated chest X-ray and select an oncologist.

If the tumour has not grown and if Daniel’s prognosis remains as optimistic as doctors testified last week, then chemotherapy and possible radiation appear to be in Daniel’s best interest, Mr Rodenberg wrote.

‘The State has successfully shown by clear and convincing evidence that continued chemotherapy is medically necessary,’ he wrote, adding he would not order chemotherapy if doctors find the cancer has advanced to a point where it is ‘too late’. If chemotherapy is ordered and the family refuses, the judge said, Daniel will be placed in temporary custody. It was unclear how the medicine would be administered if the boy fights it.

Calvin Johnson, an attorney for Daniel’s parents, said the family is considering an appeal. For now, he said, Daniel is following the order and will have X-rays Monday.

Daniel was diagnosed with Hodgkin’s lymphoma in January and it was recommended he have six rounds of chemotherapy. He underwent one round in February, but stopped after that single treatment. He and his parents opted instead for ‘alternative medicines,’ citing religious beliefs.

Doctors have said Daniel’s cancer had a 90 per cent chance of being cured with chemotherapy and radiation. Without those treatments, doctors said his chances of survival are 5 per cent.

Child protection workers accused Daniel’s parents of medical neglect, and went to court seeking custody. — AP

______

Related

Judge rules family can’t refuse chemo for boy

AP | May 16, 2009

By AMY FORLITI

MINNEAPOLIS (AP) — A Minnesota judge has ruled that a 13-year-old boy with a highly treatable form of cancer must seek conventional medical treatment over his parents’ objections.

In a 58-page ruling Friday, Brown County District Judge John Rodenberg found that Daniel Hauser has been “medically neglected” and is in need of child protection services.

Rodenberg said Daniel will stay in the custody of his parents, but Colleen and Anthony Hauser have until May 19 to get an updated chest X-ray for their son and select an oncologist

The judge wrote that Daniel has only a “rudimentary understanding at best of the risks and benefits of chemotherapy. … he does not believe he is ill currently. The fact is that he is very ill currently.”

Daniel’s court-appointed attorney, Philip Elbert, called the decision unfortunate.

“I feel it’s a blow to families,” he said. “It marginalizes the decisions that parents face every day in regard to their children’s medical care. It really affirms the role that big government is better at making our decisions for us.”

Elbert said he hadn’t spoken to his client yet. The phone line at the Hauser home in Sleepy Eye in southwestern Minnesota had a busy signal Friday. The parents’ attorney had no immediate comment but planned to issue a statement.

Daniel was diagnosed with Hodgkin’s lymphoma and stopped chemotherapy in February after a single treatment. He and his parents opted instead for “alternative medicines” based on their religious beliefs.

Child protection workers accused Daniel’s parents of medical neglect; but in court, his mother insisted the boy wouldn’t submit to chemotherapy for religious reasons and she said she wouldn’t comply if the court orders it.

Doctors have said Daniel’s cancer had up to a 90 percent chance of being cured with chemotherapy and radiation. Without those treatments, doctors said his chances of survival are 5 percent.

Daniel’s parents have been supporting what they say is their son’s decision to treat the disease with nutritional supplements and other alternative treatments favored by the Nemenhah Band.

The Missouri-based religious group believes in natural healing methods advocated by some American Indians.

After the first chemotherapy treatment, the family said they wanted a second opinion, said Dr. Bruce Bostrom, a pediatric oncologist who recommended Daniel undergo chemotherapy and radiation.

They later informed him that Daniel would not undergo any more chemotherapy. Bostrom said Daniel’s tumor shrunk after the first chemotherapy session, but X-rays show it has grown since he stopped the chemotherapy.

“My son is not in any medical danger at this point,” Colleen Hauser testified at a court hearing last week. She also testified that Daniel is a medicine man and elder in the Nemenhah Band.

The family’s attorney, Calvin Johnson, said Daniel made the decision himself to refuse chemotherapy, but Brown County said he did not have an understanding of what it meant to be a medicine man or an elder.

Court filings also indicated Daniel has a learning disability and can’t read.

The Hausers have eight children. Colleen Hauser told the New Ulm Journal newspaper that the family’s Catholicism and adherence to the Nemenhah Band are not in conflict, and that she has used natural remedies to treat illness.

Nemenhah was founded in the 1990s by Philip Cloudpiler Landis, who said Thursday he once served four months in prison in Idaho for fraud related to advocating natural remedies.

Landis said he founded the faith after facing his diagnosis of a cancer similar to Daniel Hauser. He said he treated it with diet choices, visits to a sweat lodge and other natural remedies.

On the Net:

* Hauser case final argument briefs:

http://www.courts.state.mn.us/?pageNewsItemDisplay&item45848

* Nemenhah Band: http://www.nemenhah.org

Categories: Child Takeover · Family Breakdown · Health & Fitness · Medical Mafia · Police State Dictatorship

Gene Revolution: Big Brother is Watching

May 9, 2009 · Leave a Comment

gattaca

The results will create a database, bringing the Sci-fi movie Gattaca to reality, enabling us to weed out the bad genes and focus on a perfect person.

Ivanhoe | May 8, 2009

ORLANDO, Fla. (Ivanhoe Newswire) — We are beginning a genetic revolution. Babies are tested and families can learn their health risks. But what are the risks of taking the test? Could your employer ask you to take one? What about your health insurer? Could it be the next form of discrimination? Who is looking at your DNA? Ivanhoe shows you how you can protect yourself.

“It’s outrageous, appalling,” Jenny Nelson told Ivanhoe.

She is furious and upset about what happened just hours after giving birth to little Caeden.

“I didn’t question it,” Nelson said. “I didn’t have any idea to ask questions or anything. I just kind of do what they told me to do.”

It’s not the genetic test that upsets her. It’s where her baby’s blood sample and sample of her other two children ended up.

“All of my children’s are banked and I had no idea,” Nelson explained.

All states require genetic testing at birth, but after the results come back, where does the blood go?

“A database of genetic test results of newborn citizens is growing in every state around the country,” Twila Brase, R.N., a board member of the Citizens’ Council on Health Care in St. Paul, Minn., said.

Brase advocates for a parent’s right to know about genetic tests.

“Oftentimes what happens is that the hospital simply does it and it doesn’t tell the parents that they have any rights to object,” Brase said.

She fears the results will create a database, bringing the Sci-fi movie Gattaca to reality, enabling us to weed out the bad genes and focus on a perfect person

“The stored information is actually owned by the health department in every state, so the baby’s DNA essentially becomes government property and then it’s up to the government to decide what they want to let researchers do with that DNA,” Brase said.

“Is it a realistic possibility to end up with a national database of genetic information? Absolutely!” Sue Blevins, founder and president of the Institute for Health Freedom in Washington, D.C., said.

The first new law to protect our genetic information goes into effect in November. The Genetic Information Nondiscrimination Act (GINA) prohibits genetic information from being used against you.

“We have seen cases of employers using genetic testing in an effort to weed out employees,” Susannah Baruch, J.D., the law and policy director at Johns Hopkins University’s Genetics and Public Policy Center in Washington, D.C., said. “The genetic tests themselves are sort of dubious scientific value and now the law says that we will not be able to ask people to take those tests either.”

Proving discrimination is difficult and knowing exactly where the information is going is almost impossible

“Once the genie is out of the bottle, it’s really hard to know what’s being done with that information,” Blevins explained. “It’s hard to get it back in the bottle.”

What if people knew Franklin D. Roosevelt would get polio? If a test proved Ronald Reagan would suffer from Alzheimer’s, would you have voted for him? How will genetic information impact your future?

It’s the fear of the unknown that kept Victoria Groves from revealing her family’s secret for years.

“Typically physicians don’t test for this disorder that’s caused by genes and so what happens by the time you are tested, your lungs are very damaged, and it’s irreversible,” Grove said. “There’s no cure.”

Grove’s own immune system is destroying her lungs.

“Your immune system, I think, takes a hit and you tend to get sick a lot,” Grove said.

Her younger sister died from alpha-one deficiency. Another sister is diagnosed with it. Then Grove was privately tested.

“I was positive and I decided not to tell anybody at that time, because I wasn’t sure of the ramifications,” Grove explained.

She feared her health insurance would be canceled, but she came down with pneumonia and was forced to tell her doctor. Experts say fearing what may happen prevents many people like Grove from getting the medical attention they need. Blevins believes laws need to be tighter. She’s fighting for the three C’s. First, the right to consent.

“Nothing is done without you — without your permission,” she explained.

Second is confidentiality.

“We need a law that says you get to determine who can see your information,” Blevins said.

And third is contract. Each person should have the right to pay for genetic tests through private companies

“If the federal government becomes the payer of everybody’s health care and everybody’s genetic test, they will have information to that,” Blevins said.

But until new rules and regulations are formed, experts say the genetic dilemma is in your hands.

“For someone considering genetic testing, understanding what’s the point of the test, how can it help me and are there any drawbacks to knowing this information about my future risk, those are all important questions and those should all be addressed by an individual in thinking about whether to have a genetic test or not,” Baruch said.

For Grove, revealing her secret helped her get better medical care. She didn’t lose her insurance and she’s getting the support she needs

“I think it’s made me stronger because I feel like I have tools and I have support,” she said.

It’s opening her eyes and ours to the benefits and the risks of genetic testing.

A recent Gallup poll revealed that 93 percent of Americans believe doctors should ask for consent to use their genetic information for research.

Categories: Big Brother Surveillance Society · Child Takeover · Dehumanization · Depopulation · Eugenics · Family Breakdown · Genetic Engineering · Medical Mafia · Social Engineering

Flu overhyped? Some say officials ‘cried swine’

May 9, 2009 · Leave a Comment

Many blame such alarms and the breathless media coverage for creating an overreaction that disrupted many people’s lives.

AP | May 7, 2009

By LINDSEY TANNER and MIKE STOBBE

CHICAGO (AP) — Did government health officials “cry swine” when they sounded the alarm on what looked like a threatening new flu?

The so-far mild swine flu outbreak has many people saying all the talk about a devastating global epidemic was just fear-mongering hype. But that’s not how public health officials see it, calling complacency the thing that keeps them up at night.

The World Health Organization added a scary-sounding warning Thursday, predicting up to 2 billion people could catch the new flu if the outbreak turns into a global epidemic.

Many blame such alarms and the breathless media coverage for creating an overreaction that disrupted many people’s lives.

Schools shut down, idling even healthy kids and forcing parents to stay home from work; colleges scaled back or even canceled graduation ceremonies; a big Cinco de Mayo celebration in Chicago was canned; face masks and hand sanitizers sold out — all because of an outbreak that seems no worse than a mild flu season.

“I don’t know anyone who has it. I haven’t met anyone who knows anyone who contracted it,” said Carl Shepherd, a suburban Chicago video producer and father of two. “It’s really frightening more people than it should have. It’s like crying wolf.”

Two weeks after news broke about the new flu strain, there have been 46 deaths — 44 in Mexico and two in the United States. More than 2,300 are sick in 26 countries, including about 900 U.S. cases. Those are much lower numbers than were feared at the start based on early reports of an aggressive and deadly flu in Mexico.

Miranda Smith, whose graduation ceremony at Cisco Junior College in central Texas was canceled to avoid spreading the flu, blames the media.

“It’s been totally overblown,” she said Thursday.

“Everyone seems to know it’s not going to kill you and it’s not as deadly as they think,” she said. “Everybody needs to just calm down and chill out.”

Craig Heyl of Decatur, Ga., said the government overreacted.

“Swine flu is just another strain of flu. People get the flu. I guess you have to call it a pandemic when it’s a widespread virus, but I don’t think the severity of it is all that concerning,” said Heyl, 43.

Public health authorities acknowledge their worst fears about the new virus have not materialized. But no one’s officially saying it’s time to relax. And experts worry that people will become too complacent and tune out the warnings if the virus returns in a more dangerous form in the fall.

“People are taking a sigh of relief too soon,” said Dr. Richard Besser, acting director of the Centers for Disease Control and Prevention.

In an interview Wednesday with The Associated Press, Besser said the outbreak in the United States appears to be less severe than was first feared. But the virus is still spreading and its future potential as a killer is not clearly understood.

“The measures we’ve been talking about — the importance of handwashing, the importance of covering coughs, the real responsibility for staying home when you’re sick and keeping your children home when you’re sick — I’m afraid that people are going to say, ‘Ah, we’ve dodged a bullet. We don’t need to do that,’” Besser said.

“The thing that’s keeping me up right now is that feeling of dodging the bullet,” he added.

Peter Sandman, a risk communication specialist, says on his Web site that reminding people the risk is still real and warning them in the future if a pandemic looks imminent “will be extremely difficult.”

“Swine flu looks to be an extremely mild pandemic if it goes pandemic at all, despite WHO warnings that it may ‘come back with a vengeance’ in the fall. People are going to be very, very skeptical,” Sandman wrote.

That concern is shared by infectious disease specialists. But elsewhere, especially online, talk of hype is rampant.

“If I hear 1+ person freaking out because of the “Swine Flu” they won’t have 2 worry about dying from it. I will kill them w/ my handbag!” read a comment Wednesday on Twitter.

“Adults are acting like a bunch of crybabies in a B-rated science fiction germ-outbreak movie, wringing their hands, whining about what to do next,” Dallas Morning News reader Mark Thompson wrote in a letter to the editor posted online Wednesday.

Kari Carsey Valente of Lake Oswego, Ore., had similar thoughts in a letter on the Oregonian newspaper’s Web site.

“Is the daily front page body count really necessary? In reading the entire content of the collected articles one learns that the H1N1 strain is not likely to be more lethal than its predecessors. Give it a rest — and lots of liquid!,” Valente wrote.

Colt Ables, 22, an economics major at the University of Texas in Arlington, said he thinks the Obama administration overreacted and unfairly tried to make it seem as if Republicans have been soft on preparedness.

“This shouldn’t be about politics or about hyping up a virus to send the American people into a panic. Do yourself a favor, wash your hands and turn off the TV,” he wrote in a campus newspaper column.

Whether the media overhyped or accurately reported the dangers is a toss-up, according to a USA Today/Gallup poll published Thursday on Americans’ views of the media’s flu coverage.

The May 5 poll also found that concern about the flu peaked a week ago. But even then, only 25 percent of Americans said they worried about getting the virus.

Dr. Robert Daum, a University of Chicago infectious disease expert, says authorities acted properly when news first broke about the new flu strain.

“It’s like overcalling a snowstorm in Chicago. You want the plows out even if it’s only going to snow a flake,” Daum said. If not, and a blizzard hits, “there will be an outcry like you’ve never seen before.”

Still, Daum says authorities have been a bit awkward in “downshifting” now that it appears the U.S. situation isn’t dire.

“I think it was right to place everyone on high alert, and now right” to say it’s time to calm down, Daum said.

Categories: Global Government · Health & Fitness · Medical Mafia · Mind Control · Order Out Of Chaos · Propaganda · Psychological Operations