Archive for February, 2008

Congress and the Natural Solutions Foundation “Boots on the Ground”

Tuesday, February 19th, 2008

Every time you take action and send an email to Congress, you are building the health freedom constituency. Not only are you letting Congress know about a particular issue, you are also letting Congress know that there is a tidal wave of voters who are watching and who care about the fact that health decisions, all of them, are private decisions, not the business of government! And you make it easier for the Natural Solutions Foundation to gain access to Congressional decision makers to let them know what we want them to do – and to not do. They know, when we walk into their offices, who we are because you have told them who you are and what you want and do not want from them. “Oh, the Natural Solutions Foundation”, they say, “We get lots of emails from your people. How can we help?” You, through your activism, provide entree to the halls of legislative power. You are the real power behind the Natural Solutions Foundation.
Some say that your communication does not matter. They are wrong. In the press of events and impacts on Congress, Members and their staff actually miss a great deal and, as a long time Senior Aide to a California Representative answered when I asked him how he keeps on top of all the issues and legislation in the Congressional system, “There is no way we can do it by ourselves. We depend on people who care about something to tell us about it and keep us informed about the legislation and the issues!”
What that means is that every time the Natural Solutions Foundation goes to Congress (and we try to go at least once a month for several days at a time), we go prepared with fact sheets, Congressional Briefings, information on legislation and suggestions for solutions to problems the Congressperson either is involved with or should be. The response is astonishing. The staffers value our input and we have been asked by members of Congress for language for new legislation to fix problems we identify and care about (often created by the industry friendly actions of agencies like the FDA) .
Earlier this month, Natural Solutions Foundation Trustee Ralph Fucetola and our Congressional Education Director, Charlie Frohman, visited Congress. Click here (http://vitaminlawyerhealthfreedom.blogspot.com/2008/02/educating-congress.html) to read Ralph’s report. Here is Charlie’s letter thanking the staff for their time (http://www.healthfreedomusa.org/index.php?p=529) and here () is Ralph’s follow up letter to Congress. need letter
On another, related front, natural supplements like DHEA, although protected by DSHEA (the Dietary Supplements Health and Education Act, 1994) which classifies nutrients as foods rather than drugs, are under attack as if they were steroids. Senator Hatch, a long time friend of supplements, defended them once again and the Natural Solutions Foundation is watching. Here (http://vitaminlawyerhealthfreedom.blogspot.com/2008/02/senator-hatch-defends-dietary.html) is Ralph’s blog on the subject.
Ralph beat back the FDA when they tried to ban DHEA last time so he is uniquely qualified to report on this battle. And it bears watching, of course, because the piecemeal attack on supplements does not let up. To the Pharma Phriendly FDA, any stick will do to beat a dog and they are determined to beat the natural medicine dog to death since it steals thAnd then there’s the problem of an out-of-control FDA. Yesterday, according to the AP, Rep. Bart Stupak (D-MI), who heads an investigative panel that conducts oversight of the agency, said in an interview with The Associated Press that FDA Commissioner Andrew von Eschenbach should step down because ‘it’s just a total lack of leadership.’ Stupak, chairman of the Subcommittee on Oversight and Investigations, said he had lost confidence in the commissioner and other top FDA officials over the handling of inspections and oversight by the agency.”

We agree and have been meeting with Congress for months on these issues. Can we take credit for this position by the Congressman? We cannot be not sure, but our boots on the ground certainly have helped to bring about this crisis in Congressional confidence in the FDA.

Take for example the FDA policy (which they have foisted on Codex and are implementing in the US as well) of criminalizing your right to communicate about, or use, the health benefits foods confer. Remember the FDA 2007 CAM Guidance setting up the FDA’s “right” to turn any food used for health purposes into “an untested drug” (like cherry juice, since it is good for arthritis)? The Natural Solutions Foundation found out from the FDA Receiver of Dockets that paper comments (e.g., letters) were not tabulated, only archived at the FDA Reading Room, and that the FDA website was “broken” and could not accept comments. Two Natural Solutions Foundation Trustees called the FDA Receiver of Dockets and persuaded her to give us HER email address so our supporters could let the FDA know how they felt about this Guidance. That meant that the Natural Solutions Foundation website was the only electronic means available in the US to submit comments to the FDA on this wildly misguided Guidance. Five hundred and eighty eight thousand Natural Solutions Foundation supporters visited our site to tell the FDA just how bad an idea they thought their Guidance was.

Of course, all of this activity costs money. We know you value our efforts to educate and help Congress do the right thing for health freedom. That’s why it makes sense to give generously and make a recurring tax deductible donation (http://www.healthfreedomusa.org/index.php?page_id=189) to the Natural Solutions Foundation. Now would be a great time! Your activism and your financial support are the life blood of health freedom.

And don’t forget to sign up for the free, secure Health Freedom eAlerts (http://www.healthfreedomusa.org/index.php?page_id=187) and ask your contacts and friends to do the same. Your voices protect our health freedom.

Thanks for your support!

Yours in health and freedom
Dr. Rima

Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org

Flu Vaccine Works on Only 40% of Viruses

Monday, February 18th, 2008

The article published on February 16, 2008 in the Posted on Sat, Feb. 16, 2008 is not available online. This article presents the same AP information.
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation

Flu season gets worse, vaccine only works on 40 percent of viruses
By Ashley Tusan Joyner – ajoyner@macon.com

Georgia is among 44 states reporting widespread flu activity, up from 31 states last week, the U.S. Centers for Disease Control and Prevention announced Friday.

“This season, we are having more widespread disease than the last couple of consecutive seasons,” said Dr. Joe Bresee, the CDC’s chief of influenza epidemiology. “But (this season) is not out of line with previous seasons in the last (decade).”

Adding to the problem, health officials report the flu shot is a good match for only about 40 percent of this year’s viruses – leaving a large portion of the vaccinated population unprotected.

H3N2, known as the Brisbane-like strain, and a Type B strain (B2) are the two predominant strains of flu virus, which are mostly resistant to the vaccine.

Other antiviral medications, such as Tamiflu, appear to treat the H3N2 strain.

This year’s vaccine was manufactured based on studies of the previous flu season, during which H3N2 and B2 did not account for the majority of cases and, thus, were not matched well in the vaccine. The process largely is based on medical prediction.

“In seasons where we have H3N2, we tend to have a more widespread season,” said Bresee, adding the strain makes the flu season more severe, citing higher cases of pneumonia and flu-related deaths.

“Most areas of (Georgia) are experiencing flu-like illness,” said Taka Wiley of the Georgia Department of Human Resources. “Metro Atlanta and coastal Georgia have the most activity at this time.”

Now is the height of the annual flu season, which began Sept. 30 and continues until May.

In Middle Georgia, the B2 strain is the version many people have contracted, according to the state’s public health department.

Described as a mild flu – mild fever, mild body aches and manageable other symptoms – the illness is causing sick people, who don’t feel all that sick, not to stay at home and recover, further spreading the bug.

The CDC tracks national flu activity based on reports from health departments and hospitals in 122 cities, including Macon. One in three people tested for the flu this week tested positive, up from last week, Bresee said.

The Family Health Center on Eisenhower Parkway, a division of The Medical Center of Central Georgia, reported to the CDC six cases of flu between Thursday and Friday, according to Dr. Hugh McLaurin, medical director.

McLaurin said the facility has treated twice as many patients for flu-like symptoms in the last week.

“We’re right in the beginning where it’s hitting Middle Georgia,” he said.

While not compatible with the two popular flu strains, health officials still urge people to get the flu vaccine.

“Even though it’s not a perfect match, it can still offer some cross protection for other strains,” said Arleen Porcell, a CDC spokeswoman. “It can also help make symptoms milder and protect the body from complications.”

Common flu symptoms include a high fever, body aches and chills, headaches, dry cough and possibly a runny or stuffy nose. A normal bout with the flu lasts one to two weeks.

Linda Holland, nurse manager at the Macon-Bibb County Health Department, said the health center has immunized more than 6,000 people since October.

Holland said young children, the elderly, persons infected with HIV/AIDS, cancer patients and others with immune deficiencies and heart or kidney disease are most susceptible to contracting the flu.

“These are the vulnerable populations that need to be especially careful,” she said.

As of Friday, the CDC reported 10 pediatric deaths from the flu. Nine of those occurred after Jan. 1.

“Pediatric deaths are tragic events,” said Bresee. “We’ve monitored them for the past four years. This year is not particularly unexpected given data from previous years.”

During the last three years, there have been approximately 60 cases of flu-related child deaths, he added.

Thursday, the World Health Organization announced its recommendation for next year’s vaccine for the Northern Hemisphere. The components are different than this year’s and now include H3N2.

Charlie Frohman’s Summary Letter, Febuary, 2008 Congressional Visits

Monday, February 18th, 2008

Dear XXX (Name inserted for each recipient)

Thanks for meeting with the Natural Solutions Foundation this past Thursday.

As explained in our meeting by “vitamin lawyer” Ralph Fucetola (who would serve as a wonderful witness in potential hearings), the vast majority of Americans want access to natural food, nutrients and therapies, and NSF hopes your Congressperson can ask HELP Chairman Kennedy to hold hearings on the smothering Guidelines from FDA, such as:

* requiring impossible scientific agreement on claims,
* threatening illegality to modalities by calling them untested CAM products,
* guaranteeing bankruptcy with untenable manufacturing practices,
* banning safe nutrients (such as ephedra and bioidentical hormones) by using unfair risk analyzes previously reserved for dangerous pharmaceuticals, and
* ignoring the role of pharmaceutical mixing when reviewing Adverse Event Reports for nutrients

These hearings need also to examine FDA’s 1995 “harmonization” requirements with the United Nation’s Codex Committee, which:

* uses WTO sanctions to impose its anti-natural therapies threats onto every nation on Earth, including the U.S.,
* follows the anti-natural therapies bias of FDA’s own representatives,
* has a Vitamin Committee that follows the European standard of treating natural nutrients as toxins, and limits dosage to 15% above the naturally occurring equivalent (a pathetically low standard, since the orange, in the case of Vitamin C, is grown in soil that is depleted by poisonous Big Agri chemicals, many of which were banned until reintroduced by Codex)
* requires irradiation of imported food,
* requires Monsanto’s growth hormone in imported milk
* prohibits Genetically Modified labeling, in case people think GMOs are risky

As you can see, the natural therapies preferred by a vast majority of Americans are threatened, and despite the congressional education by NSF of HELP and Energy and Commerce members going back to last Spring, no one in Congress yet has agreed to shine a light on FDA and Codex. May we count on your office to help move this process forward? If you do, please let us know and we’ll be glad to let our several hundred thousand member grassroots list know of your Leadership.

Meanwhile, below is our most recent eNewsletter. Please feel free to sign up, so you can become more familiar with our heavy involvement with countries around the world in opposing Codex and, here in the U.S., opposing FDA’s aggressive policies.

Spraying the LBAM: No Threat, No Loss, No Tests, No Sense

Sunday, February 17th, 2008

The California Department of Agriculture appears to have lost its sanity. Spraying an untested pesticide (a “plasticized pheromone”) which has never been tested for safety on people every 30 days over the San Francisco Bay area against a pest which has never infested the crops of the area or caused any crop damage while acknowledging that the substance could cause serious [fatal?] harm to people seems to make sense to them.

It does not make sense to me, but then, I am not on anyone’s payroll who makes these substances and will reap $74.5 million dollars for spraying the untested pesticide “CheckMate” over cities (and wild habitats neighboring) Monterey, Santa Cruz, Alameda, San Jose and San Francisco at least once every month until 2010. Does the same financial independence exist among the people who applied for an “emergency exemption from registration” from the U.S. Environmental Protection Agency? This exemption, for an emergency that does not exist, allows the agency to use the pesticide in aerial sprays over California cities. Because of that exemption, the spraying program is not subject to state approval, according to representatives of the state Department of Pesticide Regulation.

Toxicity tests on CheckMate itself were apparently never conducted, nor were such tests conducted on the combined ingredients in the product. Toxicity test were carried out with “other leptidopteron pheromones” [i.e., compounds similar to the active ingredient in Checkmate] which apparently allowed the CFDA to conclude that all pheromones of that nature are similar [a highly questionable conclusion] yet the 75% or so other ingredients in CheckMate were not tested. “Inert ingredients” like the ones in Checkmate can be highly biologically active and pose significant threats to people, animals and ecosystems.

In fact, on Jan 5, 2008 the CDFA admitted that they had “neither the jurisdiction nor expertise to conduct an epidemiological study of the complaints, and no public health agency at this point has said they will review the illness claims.” That means that the symptoms reported during spraying of CheckMate over Monterey (which included asthma, coughing, muscle aches and headaches, as well as any long term impacts to either single exposures of monthly exposures over a 5 year period as currently planned for the Bay Area may well be the harbingers of major health problems for the millions of people exposed to this untested substance.

When local activists challenged the spraying in Santa Cruz on October 10, 2007, Judge Robert O’Farrell issued a temporary restraining order that which stopped the area’s second round of spraying until Oct. 18, when a hearing was scheduled to consider additional evidence in a lawsuit filed by Peninsula activists.

O’Farrell named the active ingredient in CheckMate— polymethylene polyphenyl isocyanate, or PPI, which is listed as a “hazardous agent” by the National Institutes of Health on the agencies’ Web site as the offending agent. The site noted reports of occupational asthma among spray painters exposed to it. Checkmate is made by Suterra.

The tests which were conducted mentioned ingestion and skin/eye application as problems, but not complications arising from inhalation. Claiming the plasticized capsules containing the pheromone are too large to directly enter the lung it is curious that the potential for irritation to the larynx, pharynx, and tracheo-bronchial passages are mentioned although apparently the safety profile in the respiratory tract was never tested.

Toxicity tests are done to determine whether the dosage is lethal but not what long term complications could arise after inhaling the substance.

Another concern about the CheckMate program is the ecological impact. There is little available information to suggest that the fragile and productive ecosystems of the Bay Area, both land and water based, will be left unharmed by the polymethylene polyphenyl isocyanate in Checkmate because no environmental impact statement has been filed.

Following you will find an article from the San Francisco Chronicle and a summary of the problems inherent in this mad scheme.

Pushback – our response to these assaults – is essential if we are to control and to safeguard our environments and our health. Help us push back! Disseminate this information, tell people about the Natural Solutions Foundation and urge them to go to the website, www.HealthFreedomUSA.org and sign up for the free, secure and informative Health Freedom eAlerts (http://www.healthfreedomusa.org/index.php?page_id=187). Natural Solutions Foundation – We are more than just talk!
Donate (http://www.healthfreedomusa.org/index.php?page_id=189)generously with a recurring tax deductible donation to the Natural Solutions Foundation, www.HealthFreedomUSA.org.

Thanks!

Yours in health and freedom,
Dr. Rima

Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation

www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org

Now, an article from the San Francisco Chronicle:

The Light Brown Apple Moth which means that no State approval is required?
State plans Bay Area pesticide spraying

Jane Kay, Chronicle Environment Writer

The [California] state agriculture department plans to use airplanes at night this summer to spray a farm pesticide over urban San Francisco, Marin County and the East Bay, intending to eradicate a potentially destructive moth.

The little-known proposal to wipe out the light brown apple moth, which if it became established could destroy the region’s agricultural industry, has developed increasing opposition among some residents who fear for their health.

Hundreds of people whose homes and yards were sprayed in Santa Cruz and Monterey counties from September to December have filed reports that said the pesticide seems to have caused coughing, wheezing, muscle aches and headaches, among other symptoms. One Monterey family reported that a child had a first-time asthma attack.

State officials say the amount of pesticide applied shouldn’t pose severe health risks, but they’ve also refused to rule out that the spray can affect humans, particularly sensitive people such as children and the elderly.

Spraying of the pesticide, called Checkmate, is expected to begin in the Bay Area in August and could continue for five years over San Francisco, Daly City, Colma, Oakland, Piedmont, Emeryville, El Cerrito, El Sobrante, Tiburon and Belvedere. Other chemicals could also be used.

Before its use in Santa Cruz and Monterey last year, the pesticide, a hormone that throws off the scents of mating moths, had been used aerially only over farms and never over populated areas.

The U.S. Department of Agriculture obtained an “emergency exemption from registration” from the U.S. Environmental Protection Agency that allows the agency to use the pesticide in aerial sprays over California cities. Because of that exemption, the spraying program isn’t subject to state approval, according to representatives of the state Department of Pesticide Regulation.

There is no widespread infestation of the light brown apple moth, but U.S. Department of Agriculture officials say they are trying to head off a potential disaster. The federal agency has given the California Department of Food and Agriculture $74.5 million to conduct the spraying program, which officials say is warranted because an international survey of pests ranks the moth high as a threat, and moths have been found in the state, primarily in the Bay Area. The little moth was first trapped in Alameda County in March. The state agricultural agency followed up and found moths in 11 counties, said Larry Hawkins, a USDA spokesman.

The moth’s larvae stunts seedlings, pits leaves and can damage fruit trees, citrus and grapes.

Its potential spread to almost every plant around, including native trees, threatens crops worth up to $640 million a year, he said. The pesticide over time reduces the moth population by interfering with its ability to reproduce and doesn’t require the use of a more toxic insecticide, Hawkins said.

Steve Lyle, a spokesman for the state agricultural department, said new trapping data for 2008 could change the aerial spray program set for Marin, San Francisco and the East Bay.

“But right now, based on what we know, it will go ahead,” he said.

In response to complaints from residents from Santa Cruz and Monterey counties, several state agencies – the Department of Pesticide Regulation, the Office of Environmental Health Hazard Assessment and the Public Health Department – issued a statement that acknowledged that eye, skin or respiratory irritations reported by residents could have been caused by high applications but not by low ones.

“The toxicological information on the Checkmate product indicates that exposure to high levels of the applied material would be consistent with many of the reported symptoms,” the statement read.

The pesticide levels used in Santa Cruz and Monterey counties were extremely low, the agencies said, making it unlikely that anyone was exposed to a high dose.

However, the statement cautioned that “not all health effects can be predicted and because the general population includes susceptible (people), such as children, the elderly and those with chronic diseases, we cannot provide a definitive cause for their symptoms.”

The USDA’s Hawkins said the EPA has generally not been concerned over the toxicity of Checkmate. For example, he said, the agency never set a maximum limit for the pesticide in food or required farm workers to stay out of fields that had just been sprayed.

“It’s not a material the EPA would have any concern about,” Hawkins said.

Many residents in Santa Cruz and Monterey counties are joining an umbrella group, California Alliance to Stop the Spray, or CASS, to fight the continuing spraying program, which is expected to resume June 1.

More than 600 people from the two counties have reported symptoms, including asthma attacks, bronchial irritation, lung congestion and soreness, difficulty breathing, coughing and eye and throat irritation.

Dr. Randy Baker, a family practitioner in Soquel, said he treated about a dozen patients with a range of symptoms when the area was being sprayed. Although he said there was no way to ascertain a cause-and-effect relationship, he had a number of concerns about the pesticide, including the fact that it was not tested for use over urban areas.

“There is tremendous individual variation in the ability of people to process and detoxify environmental chemicals. For example, there could be a prescription medicine that 100 people take with minimal adverse effect but another person could take it and suffer extreme side effects and even death,” Baker said.

Baker was also shocked that the agricultural department started spraying the chemical on an evening when people were out walking in Santa Cruz.

“At 8 p.m., they started spraying in the most populated areas of Santa Cruz County. I have patients who didn’t know the spray was happening who were out walking on Mission Avenue. Clearly, the greatest danger is a person being out of doors when the planes are going over. They’re going to be inhaling the chemicals,” Baker said.

Further complicating the issue is that some residents say they simply don’t trust the government information. The pheromone is not the only chemical in the spray. Checkmate also contains at least 10 other ingredients.

The product contains a surfactant, which could have coated the more than 600 birds that turned up injured after the spraying last year as far north as Año Nuevo and south to Del Monte Beach in Monterey, they say. Government agencies attributed the substance that coated the birds to algal changes.

Elizabeth Quinn, a resident of Santa Cruz, is among those opposed.

On Nov. 9, starting at midnight, the planes flew 500-feet above Quinn’s house in Santa Cruz until 5:30 in the morning.

“They came over every 20 to 30 minutes, back and forth, back and forth,” she said. Quinn didn’t suffer any health problems after the sprays, but she is worried about the people who did.

“I have 6-year-old and 3-year-old grandsons,” she said, “and I’m very concerned about their health.”

Also Thursday, about 80 people turned up at a hearing held by Assemblyman Jared Huffman, D-San Rafael, who heads the Assembly’s Environmental Safety and Toxic Materials Committee. State health and agricultural officials and members of nonprofit groups presented details of the pending program, and most of the public that spoke were concerned about aerial spraying.

Last month, the Albany City Council voted unanimously to oppose the spraying, and the nonprofit Center for Environmental Health started holding meetings, the first in Oakland, to address questions from worried residents.

A series of meetings is scheduled this month to discuss the environmental reports of the moth-eradication program in the Bay Area.
Light brown apple moth

Problem: Larvae of the tiny moth, a native of Australia and much smaller than a penny, feeds on more than 2,000 plants and trees.

Eradication: Officials plan to spray pesticide to disturb its mating. More information: links.sfgate.com/ZCLW.

Source: California Department of Food and Agriculture

And an article listing the problems with LBAM spraying:

STOP AERIAL PESTICIDE SPRAYING IN CENTRAL AND SOUTHERN MARIN

What’s wrong with the LBAM spraying?
1.Hundreds of people in Santa Cruz and Monterey County have reported adverse health reactions. The spray has not been tested for long-term human toxicity and is being applied in microscopic plastic capsules that could pose inhalation risks.
2.The spray contains ingredients that are highly toxic to aquatic species, as well as surfactants, that might have contributed to algae bloom (red tide) and the death of hundreds of waterfowl.
3.Biologists agree that the spraying – an outdated, unsustainable, expensive pest control method – will not eradicate the moth. The CDFA should switch to a control vs. an eradication program using least-toxic methods that farmers already apply, e.g. sticky traps.
4.CDFA itself says the moth has done no crop damage in California to date. Priority must be given to public and environmental health and safety over speculative economic loss.
5.The aerial spray program disproportionately impacts vulnerable segments of the population, including those with the recognized disability of multiple chemical sensitivity, who are in many cases forced to relocate, and the homeless, who have no option to protect themselves from spraying.

Now For A Little Pharma Phun: How About Some Mother/Baby Abuse

Sunday, February 17th, 2008

“Thirty years ago…Merck’s aggressive chief executive Henry Gadsden told Fortune magazine of his distress that the company’s potential markets had been limited to sick people. Suggesting he’d rather Merck to be more like chewing gum maker Wrigleys, Gadsden said it had long been his dream to make drugs for healthy people. Because then, Merck would be able to “sell to everyone.” Three decades on, the late Henry Gadsden’s dream has come true.”
Alliance for Human Research Protection

Mothers, unborn babies and infants are the next group to “sell to”. If Congress has its way, every pregnant mother and her unborn baby, every new mother and her (perhaps) nursing infant in the US would be someone to “sell to”, not just by Merck, but by the entire pharmaceutical industry. Click http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=23065(http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=23065) to tell your Senators and Representatives that pregnant and new moms do not need drugging with meds that increase suicide and homicide and harm babies. Let them know that mental health decisions – like all health decisions – are a private matter, not a government one.

A new and shameless market ploy called “The Mother’s Act”, S 1375 IS (http://www.healthfreedomusa.org/index.php?p=527), would make them the next market success by compelling screening and “offering” “appropriate” treatment which includes, as the bottom line, drugs. The bill was originally proposed in response to the death by suicide of Melanie Stokes, a pharmaceutical rep.who took her own life by leaping from a balcony several stories off of the ground. Contrary to popular understanding it was not post-partum depression that killed Melanie, but the numerous antidepressant drugs she was taking, which the FDA confirmed double the suicide risk.

In my professional opinion as a Child, Adult and Adolescent Psychiatrist and in my opinion as a health freedom advocate, the so-called “Mother’s Act” represents an act of aggression against mothers, babies and liberties, all at the same time. Pregnant woman and infants, along with new mothers and their babies, are an untapped market for psychoactive drugs like anti-depressants and anti-psychotics. There is an excellent reason that they are an untapped market for these drugs. Because they are so dangerous for these groups of people, these drugs, like most others, have been strictly off limits for pregnant and nursing moms and their babies.

But no longer. If Senators MENENDEZ (D-NJ), DURBIN (D-IL), SNOWE (R-ME), BROWN (D-OH), DODD (D-CT), and LAUTENBERG (D-NJ) have their way, pregnant mothers will be “screened” for tendencies toward “postpartum blues”, “depression” and “psychosis” and offered medications if they show any such tendencies. Another new market opened for the Pharma Pholks!

To my knowledge, this would bring to eight the number of pieces of Federal Legislation which make it possible to compel people living in the United States of America to take medication or set the stage for state compulsion to take those meds. The mis-named Patriot Act, Patriot Act II, BioShield, BioShield II, BioShield III, New Freedoms Initiative, No Child Left Behind and now the “Mother’s Act”.

Picture this scenario: a mother to be confesses to being nervous, worried, anxious or concerned about the impact of the coming baby (Signs of mental health in my book, by the way). A nurse, social worker, “counselor” or doctor turns her concern into pathology on a “screening tool” called a piece of paper (or computer screen). Mom’s public medical record (there are no confidential medical records in the US any longer unless you go to a physician who has exempted him/herself from HIPAA, [Health Insurance Privacy and Accountability Act] and pay for the services yourself) now states that she has a mental illness. Next, she will be “offered” drugs to “help her” with her normal feelings. These are the proverbial drugs for the worried well. What happens if they decide not to take them? Could mothers be forcibly imprisoned or held in a psychiatric facility? Of course they could. How about moms who have already given birth: could the same happen to them or could they loose custody of their children if they decided not to take the advice of the screener and take meds? You bet. Consider the invasive and unconstitutional losses of parental rights when parents do not medicate their kids. Consider the cases where chemotherapy or Ritalin (c) or Zoloft (c) or whatever have been forced upon kids and grown ups. Consider the forcible vaccination – and re-vaccination – of 2,700 Prince George’s County (MD) poor, mostly black children (1100 of whom had already been vaccinated fully but whose records had been lost by the school (according to its own admission).

Consider this fact: the March of Dimes advises against the use of these drugs in pregnant women since they can cause birth defects. Consider, too, the fact that the numerous psychiatric drugs which the woman who killed herself in the post partum period, Melanie Stokes, a pharmaceutical rep. (who took her own life by leaping from a balcony several stories off of the ground) doubled her risk of suicide according to the FDA while being a post partum mom did no such thing.

According to the officers of “Unite”, an organization opposing this legislation and the use of all other psychiatric medications,

“To simply screen women for post-partum mood disorders and ensure that they get “treatment,” we would be setting families up for the expectation of tragedy and increasing the chances of that actually happening when we refer them to medical “professionals” who are oblivious to the negative mind-altering effects of psychiatric drugs. A popular opinion among medical caregivers these days is that “post-partum mood disorders” must be a sign of an underlying biochemical imbalance and would be corrected with drugs.

Current drugs used on post-partum women include SSRIs, atypical antidepressants, and even antipsychotic drugs. These pose a significant risk to the immediate safety and health of women as well as their children and families. SSRIs carry a black box warning for suicide and the most popular one, Effexor (the same med. Andrea Yates was taking when she drowned her 5 children), has the words “homicidal ideation” listed as a side effect. “Nearly every recent case of infanticide which has made news can be clearly linked back to a psychiatric drug. These drugs endanger babies and mothers.”

Additionally, the drugs can be extremely addictive and also pose a risk to nurslings or babies exposed in subsequent pregnancies. Some babies have died from SIDS linked to drug exposure from pregnancy or nursing; others have experienced coma, seizures, GI bleeding, heart defects, lung problems, and many babies died before reaching full term or soon after birth” when their moms have been exposed to these drugs.

The bill does not address the fact that studies show that biological agents (antidepressants for example) cited in the bill and already prescribed to pregnant women can cause congenital heart birth defects where children have had to undergo open-heart surgeries to correct this. Also, some babies are being born with organs outside their bodies, requiring immediate surgery.”

Never mind that these drugs are untested in large scale use during pregnancy and are listed as drugs to avoid while pregnant and nursing. Never mind that the March of Dimes and the Physician’s Desk Reference (PDR) advise avoiding these drugs during those time. Never mind that the American Academy of Pediatrics cites an article which says, “Our knowledge [of the impact of psychiatric drugs on the fetus] will remain limited because prospective, randomized, and well-controlled investigational studies on the risks of exposure to psychoactive drugs during pregnancy are neither feasible nor ethical” in its Policy Statement on the Use of Psychoactive Medication During Pregnancy and Possible Effects on the Fetus and Newborn.

They also state, “Potential adverse effects for the fetus and the neonate include: 1) structural malformations, 2) acute neonatal effects including intoxication and neonatal abstinence syndromes, 3) intrauterine fetal death, 4) altered fetal growth, and 5) neurobehavioral teratogenicity. Neurobehavioral teratogenicity encompasses long-term central nervous system defects that result in delayed behavioral maturation, impaired problem solving, and impaired learning. Physical malformations do not necessarily accompany the functional deficits. Chronic in utero exposure to drugs may result in intoxication or tolerance postnatally. Neonatal drug withdrawal symptoms may occur when drug exposure ceases at birth. Specific and supportive therapy may be required if the newborn displays signs of continued drug effects or withdrawal. Long-term developmental and neurologic follow-up is appropriate, including consideration for referral to centers for national databases (eg, Teratology Information Services and Motherisk Program).” But never mind. A market is a market and this one is nearly virgin since the drugs in question have had posted warning advising their avoidance in pregnancy and nursing.

And what a market it is! The text of the bill states that although “The causes of postpartum depression are complex and unknown at this time” (which means that treatment designed to suppress the symptoms without dealing with the cause is a poor way to go), the market is vast since, ” Baby blues afflicts up to 80 percent of new mothers, postpartum depression occurs in 10 to 20 percent of new mothers, and postpartum psychosis strikes 1 in 1,000 new mothers.”

I am a Psychiatrist. I am trained in Child, Adolescent and Adult Psychiatry and I have a bias. I believe that drugs are dangerous and, in the case of psychiatric drugs, outstandingly dangerous, often causing long-term damage to the nervous system and other organs which are then treated with more drugs since the signs of drug toxicity are virtually identical to the reasons the patient was given the drug(s) in the first place, only more so. These drugs, increasingly used on the vulnerable nervous systems of younger and younger children with no deep understanding of their impact on the developing brains and bodies are poorly tested, vastly oversold and represent a huge profit center. Their only problem, from the point of view of the pharmaceutical industry, is that there are large markets which are currently untouched. Once these drugs are administered, for whatever reason, they tend to become a legal habit supplied by your friendly pusher, your doctor. Although your pusher may be well-intentioned, his/her information about the safety and efficacy of these toxins (and make no mistake: they are known brain and liver toxins with a hefty dollop of endocrine disruption, pancreatic destruction and liver damage throw in for good measure) comes from the very people who make a profit from his/her use of these substances.

There is now, following nearly endless revelations in Congressional hearings, leaked information, legal actions against drug companies, etc., a clear patter of corruption and collusion to place dangerous drugs on the market and keep them there between the FDA and the manufacturers of these compounds.

With the collusion of the FDA, information on the dangers of these drugs, their tendency to increase suicidal and homicidal behaviors and their addictive impact are suppressed or minimized while new markets are sought out to allow the dream of Henry Gadsen to come true.

I think not! Remember, if we all think not, then we need to create a strong and effective grass roots organization to take this message to Congress (that’s what your emails do and what our Congressional education program does) and to the rest of America. That’s where your support comes in. Send this blog to your list. Ask them to visit the Natural Solutions Foundation website, www.HealthFreedomUSA.org and sign up for the free, secure and informative Health Freedom eAlerts (http://www.healthfreedomusa.
org/index.php?page_id=187
).

And don’t forget donations: we really need your financial help. Your tax deductible donations make our work possible. Please consider making a generous recurring donation (http://www.healthfreedomusa.org/index.php?page_id=189) right now.

Natural Solutions Foundation and You: Together We are More Than Just Talk!

Yours in health and freedom,

Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org