Archive for the ‘Legislation to Oppose’ Category

GSK’s Citizens Petition to Treat Supplement Weight Loss Claims as Disease Claims

Tuesday, May 13th, 2008

Maybe you take weight loss supplements and maybe you don’t. But protecting them, and the claims that the FDA recognizes are appropriate for them, has become a matter of urgency since GlaxoSmithKlein (GSK)has attacked the entire supplement industry through direct threat to our supplements and the entire supplement industry. GSK is using two arrows aimed at the heart of the supplement industry. A copy of the GSK attack is reprinted below this blog entry.

Two Pronged Assault

1. Restrict the information that helps people understand what a product does for them (and cripple the First Amendment while you are at it) and

2. Medicalize a category of concern for people taking the supplement and then make sure that the health indications and claims, as well as the supplement are “oozed over” into the drug category, raising their prices and driving their manufacturers out of business while more expensive drugs take their places in the customer’s shopping cart.

In my lecture “Nutricide ” ( http://tinyurl.com/2kvnvt ), I defined Nutricide as

1. The death of the body of knowledge of the relationship between health and food and

2. The death of large populations through the manipulation of the food supply.

GSK vs. The People

GlaxoSmithKlein, a large drug company, has decided to use the powerful tool called a “Citizens Petition” to attack both free speech and the supplement industry. The Citizens Petition is the same type of document that the Natural Solutions Foundation has filed twice with the US Government).

Sign the first Citizens Petition here ( http://www.healthfreedomusa.org/index.php?page_id=184 ) to demand the FDA stop illegal “HARMonization”. Our second Citizens Petition, like the current GSK one, has not been assigned a Docket Number (and, for that matter, has ours?) so you cannot comment on it yet. We will tell you how to do that shortly.

(By the way, if you are a supplement manufacturer and you are not very happy with the lobbying representation you are getting on Capital Hill, send us an email (ralph.fucetola@usa.net) with “PROTECTION” as the subject line to join the Health Freedom Alliance, a Wellness Industry 501 (c) 4 organization we have created just for you!)

By asking the FDA to define weight loss products as disease claims, they are protecting their failed over-the-counter weight loss product, alli , while striking a blow at the continued existence of the entire supplements industry. Once weight loss is a disease, not a condition, it will be treatable only through the use of tested drugs. Will insurance companies increase your rates if you need weight loss products? Possibly. After all, we understand that many insurance companies are co-owned by Big Pharma. More diseases, more drugs. More drugs, more profits.

Click here ( http://tinyurl.com/4txv62 ) to let Congress know your right to free speech and information about the relationship between health and supplements are important to you!

(If you want a copy of “Nutricide: the DVD”, click here ( http://www.healthfreedomusa.org/index.php?page_id=156 ).

Supplements Under Attack – Again!

GlaxoSmithKlein (GSK) makes drugs like Paxil and Avandia, the highly questionable diabetes drug which the FDA knew nearly 5 years ago increases heart attacks by nearly 43%. Covering itself, the FDA recently issued a warning to GSK about supressing data about the dangers of this supposed “block-buster” drug. Not long before that, the Senate Finance Committee found that GSK intimidated and coerced a well-known critic of Avandia to silence him from speaking out against it. And not long before that, there were serious allegations that GSK had supressed data on Paxil-related adult suicides.

GSK is also the maker of alli, the first over the counter weight loss drug. Alli has been associated with the development of aberrant crypt foci, widely believed to be associated with the development of colon cancer. It is also associated with fecal leaking, “wet gas”, diarrhea, and a sudden event where you could at any moment have an uncontrolled accidental bowel movement. Natural products are not associated with these hazards. So it would seem that anything GSK could do to silence the natural competition and grab a new market share would be welcome to its management and its shareholders.

In fact, here is what www.FDAlawblog.net has to say about the GSK Citizens Petition:

“the Citizens Petition asks the Agency (i.e., FDA, ed. ) to prohibit structure/function claims for dietary supplements that expressly or impliedly reference weight loss. In addition to claims that expressly reference weight loss, the petition contends that the following categories of claims should be prohibited: energy expenditure, modulation of carbohydrate metabolism, increased satiety or suppression of appetite, increased fat oxidation or reduced fat synthesis, and blockage of fat absorption. The petition acknowledges FDA’s longstanding position that weight loss claims are permissible structure/function claims. However, the petition urges FDA to change its position on the ground that: (1) recent evidence establishes that overweight is a risk factor for disease; (2) consumers believe that there is a relationship between weight loss and a reduction of risk of disease; (3) claims that a product will reduce a risk factor for disease are disease claims; (4) the use of ineffective therapies can divert consumers from safe and effective therapies such as GSK’s weight loss drug Alli; and (5) manufacturers of weight loss supplements should be forced to substantiate their claims through health claim petitions before going to market. Although the petition targets dietary supplements, the action it requests also would affect conventional foods.

The potential marketing value of the weight loss market and the food and dietary supplement industries’ major investment in weight loss products ensures that the petition will receive strong drug industry supported and vigorous food and dietary supplement industry opposition. Although the petition contends that the requested action will not require rulemaking, there are arguments that would support the need for rule making given FDA’s longstanding position that weight loss claims, as opposed to claims to treat obesity, do not imply disease treatment or prevention.”

Taking advantage of the tremendous power of the Citizens Petition, GSK is asking the FDA to classify weight loss claims made for dietary supplements as disease claims. While the distinction may seem small, what it means to your supplement access could be very bad, indeed. If the FDA finds for GSK, it will make it much easier to classify nutrients as drugs and much harder to make truthful and honest statements about the health benefits of supplements.

This is just another thrust to find yet another way to destroy the supplement industry NOT because it is bad or dangerous, but because just the opposite is true: drugs are dangerous and kill people. They are also very expensive.

Supplements are relatively cheap, very safe and do not kill people. They are, however, the greatest economic competitior to drugs and therefore the drug companies want them to disappear. They are, of course, very willing to help them do just that!

The rapidly growing weight loss sector of the supplement market in the US is about $1.3 Billion, or about $1 of every $25 spent on supplements and herbs annually. Many supplement companies depend upon these products for significant sales and staying afloat in a challenging market place.

I find it hard to see it as a coincidence that the alarming ” Trilateral Cooperation Charter ” ( http://www.fda.gov/oia/charter.html), signed February 27, 2004 fusing

* Health Products and Food Branch,Health Canada

* US Food and Drug Administration, Department of Health and Human Services

* Federal Commission for the Protection from Sanitary Risks, Secretaria de Salud, Mexico

has decided that one of its very first priorities is eliminating so called health fraud by “enforcement action on Fraudulent weight loss products” ( http://www.fda.gov/oia/charter.html#appendixc ). The Trilateral Cooperation Charter defines fraud as “the false, deceptive, or misleading promotion, advertisement, distribution, sale, possession for sale, or offering for sale of products or provisions of services, intended for human use, that are being represented as being made safe and/or effective to diagnose, prevent, cure, treat, or mitigate disease (or other conditions), to rehabilitate patients or to provide a beneficial effect on health.” If you are hearing that as an invitation to destroy the supplement industry in the US, Mexico and Canada (also known as the North American Union/Security and Prosperity Partnership), you are hearing right.

Given the battle raging a round the right to make true and honest statements about the healing benefits of foods or food components, it would appear GSK’s attempt to silence its competitor is simply more of same. Codex wants to classify sharing any information about the health benefits of food and food components as “advertising”. The FDA wants to stifle the same information by calling it “health claims” or, in this case “disease claims”. The net result, if we allow them to have their way? Regulatory duct tape over our collective mouths if we dare to share information about how to get well and stay that way with natural products. Not today, not tomorrow and not any time after that!

Opportunity

Did I mention that the Natural Solutions Foundation is gearing up to go to the Codex Commission Meeting in Geneva in late June? Not only will we be there, but we expect to serve as advisers to a coalition of health friendly nations who have been preparing for the “push back” against the US on the issue of mandatory, species specific GMOs labeling.

As you know, the US forbids – FORBIDS – labeling any GM Foods. Most of the rest of the word is fiercely determined to have such labeling. The health friendlies are on the march!

We need your help to get there, though. Take a few minutes to send us forward to Geneva for the Annual Codex Commission meeting.

Click here to make your tax deductible donations ( http://www.healthfreedomusa.org/index.php?page_id=189 ).

Thanks for your continuing support! We are the largest and most effective health freedom force in the English speaking world! We make a great team!

CDC: Immunize Every Kid in America Against Flu – Every Year! Hey, It Worked in NJ!

Thursday, February 28th, 2008

The CDC and the American Academy of Pediatrics have succeeded in New Jersey so they are now after every child in America: vaccinate every child every year with flu shots that damage the immune system, may contain mercury, surely contain aluminum, formaldehyde, foreign protein, and actually don’t work most of the time. Apparently that sounds like a winner to the Big Pharma side of the house.

There are twists of logic that boggle the mind here. For example, although the CDC admitted within the last month that this year’s seasonal flu shot is only effective 40% of the time or less since the viruses in circulation are not the ones covered by the vaccine, there is no let up in the insistence that every child get vaccinated with this flu shot.
Consider, too, the rather astonishing quote from the article below:

“No deaths have been reported in New Jersey this season, but 16 children have been hospitalized with confirmed cases of flu, state
health officials said. Flu activity is currently characterized by the CDC as “widespread” in New Jersey.”

Does that mean that 16 kids with severe immunocompromise problems (say, kids on chemotherapy for cancer) or kids with HIV/AIDS got the flu and needed to be hospitalized and so every kid in the country needs to be vaccinated with a dangerous shot? What about the lost days and hours and lives of parents who have kids who have been vaccine injured and suffered brain injury, autism, asthma, or cancer? And what about the loss of parental rights and liberties guaranteed by the Constitution of the United States? Is that worth protecting the employers of New Jersey and the US from lost days of work by the parents whose kids get the flu (most often a cold, by the way)?

Apparently it does.
And then there is the rather weird “logic” of vaccinating kids yearly to protect their parents from loosing time from work (last year it was “vaccinate the kids to protect the elderly with whom they might come into contact”). You will note the same arguments used in New Jersey before the Health Commissioner declared that every child in the state, starting in infancy, would have to be vaccinated annually if they wanted to attend day care or go to school.

It is rumored in New Jersey that when Governor Corzine’s Stem Cell Therapy initiative failed to give the Big Pharma companies headquartered in that State the huge give away they were anticipating, he felt compelled to do something to help these companies (like Merck) want to stay in NJ. Reasoning that annual vaccination of kids might be a good gift to his Pharma Phriends, the Governor, who has been provided with all the scientific information needed to make it clear that this is a very, very bad idea, decided to go ahead anyway. A real “Man of the People”, as long as you are talking about Pharmaceutical investors and executives.

Read today’s entry into the “Vaccinate Every Kid Every Year” Propaganda campaign.

Compulsory vaccination is just part of the plans afoot for compulsory drugging. Please take all of the following Action Steps to protect your rights to make your own health decisions, not have them forced upon you by the Pharmaceutically controlled policy makers.

1. STOP COMPULSORY DRUGGING AND VACCINATION (http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=21835)

2. SUPPORT PHILOSOPHICAL EXEMPTIONS IN NEW JERSEY AND ALL OTHER STATES (http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=23087)

3. STOP SCHOOLS FROM FORCING DRUGS ON KIDS
(http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=18970)

4. PREGNANT AND NEW MOMS DON’T NEED FORCED DRUGGING THAT COULD INJURE OR KILL THEIR BABIES
(http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=23065)

These actions steps are vitally important in the movement toward passive helplessness in the face of Big Pharma domination of public policy toward active citizen control of our own health decisions.
Please support this change by taking the steps, letting everyone in your circle of influence know about them and making a recurring donation to the Natural Solutions Foundation by clicking here (http://www.Healthfreedomusa.org/index.php?page_id=189) to make your tax deductible donation.

Yours in health and freedom,
Dr. Rima

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

CDC panel expands flu shot guidance: Children up to 18 should get vaccine
Thursday, February 28, 2008
BY ANGELA STEWART
Star-Ledger Staff
Every child up to the age of 18 should be immunized against the flu,
a federal advisory panel recommended yesterday.

The recommendation, made by the Centers for Disease Control and
Prevention’s Advisory Committee on Immunization Practices, would
increase the number of children receiving flu shots by 30 million a year. Children younger than 6 months are excluded.

It is expected to be approved by the CDC as early as this spring and
become the agency’s official policy for the 2008-2009 flu season.

“We don’t expect any issue with this recommendation,” said Curtis
Allen, a CDC spokesman.

The CDC’s previous recommendation was that children from 6 months to
5 years of age or those with chronic conditions that put them at high
risk of complications needed to be immunized.

Allen said the expanded recommendation — which would be advisory but
likely influential — is pri marily aimed at protecting healthy
children of all ages against the flu, but noted it will also offer
residual benefits to others.

“The logic is there are children in this 6-month to 18-year-old age
group who are in schools where we know a lot of influenza
circulates,” he said. “When a child becomes sick, a parent also has
to stay home and out of work, which is lost productivity. Once a
child is vacci nated, this will help protect others in their
household and the community from influenza.”

A representative of the American Academy of Pediatrics applauded the
recommendation, saying there are many children with conditions like
asthma who should be getting immunized but aren’t.

“We know that the vaccine is the best method for preventing influenza
and its potential severe complications,” said Henry Bern stein, a
member of the academy’s committee on infectious diseases and chief of
pediatrics at Dartmouth Medical School in New Hampshire

Children have among the highest rates of flu of any age group,
according to the CDC, with more than 20,000 kids under the age of 5
hospitalized each year nationwide. So far this flu season, 22
children across the country have died from flu-related illness, Allen
said.

No deaths have been reported in New Jersey this season, but 16
children have been hospitalized with confirmed cases of flu, state
health officials said. Flu activity is currently characterized by the
CDC as “widespread” in New Jersey.

Maria Spina of Colonia, whose 7-month-old daughter, Carlee, received
a flu shot yesterday at the office of Nutley Pediatrics, said she
thought the recommendations made sense.

“I think any mother would worry if their child got really sick with
the flu,” Spina said.

Richard Marcus, who immu nized Spina’s baby yesterday, said many
parents take vaccine preventable diseases “very, very, lightly.”

“It’s seen as something that doesn’t affect their children, that is
until they have an episode,” Mar cus said. “Then they become firm
believers.”

Alissa Kanowitz, who was a founder of a group called Families
Fighting Flu, lost her 4-year-old daughter Amanda in 2004 to the flu.
Amanda was not immunized, as the CDC at the time only recommended
shots for children up to 23 months. Two years ago, the recommendation
was expanded to include children up to age 5.

“Today’s vote really sends a strong message about just how se rious
influenza is,” said Kanowitz, a New York City resident.

This fall, New Jersey will become the first state in the nation to
require flu shots for infants and children entering licensed day care
centers or pre-schools. The state Public Health Council passed that
recommendation despite protest from anti-vaccine groups and oth ers
who oppose what they view as government usurping parental authority.

State Epidemiologist Eddy Bresnitz said that while he embraces the
new recommendations, New Jersey has no plans to make them mandatory.
Bresnitz, however, said he sends out an annual letter through schools
encouraging parents to have their children im munized against the flu
and will mention the CDC recommendations next fall.

Sue Collins, who co-founded the anti-vaccine advocacy group New
Jersey Alliance for Informed Choice, called the CDC’s new “blanket”
recommendation for pediatric flu shots a bad idea.

“I think the risks and side ef fects and unproven safety and effi
cacy studies do not warrant this,” said Collins, a mother of two who
lives in Long Hill. “The biggest thing is there is no data on how all
these vaccines react with each other.”

State and federal health officials, as well as most doctors, be lieve
the flu vaccine is safe for children, but many parents have raised
objections about the fact it contains thimerosal, a mercury-
containing organic compound used as a preservative in some multi-dose
vials of vaccine.

But there is flu vaccine doctors can order that is free of the
preservative, although it costs slightly more than the traditional
vaccine. Children, starting at 24 months, also have the option of
receiving a flu nasal spray instead of a shot.

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

Text of “Mother’s Act”, S. 1375

Sunday, February 17th, 2008

Source: Thomas.loc.gov


MOTHERS Act (Introduced in Senate)

S 1375 IS

110th CONGRESS

1st Session

S. 1375

To ensure that new mothers and their families are educated about postpartum depression, screened for symptoms, and provided with essential services, and to increase research at the National Institutes of Health on postpartum depression.

IN THE SENATE OF THE UNITED STATES

May 11, 2007

Mr. MENENDEZ (for himself, Mr. DURBIN, Ms. SNOWE, Mr. BROWN, Mr. DODD, and Mr. LAUTENBERG) introduced the following bill; which was read twice and referred to the Committee on Health, Education, Labor, and Pensions

A BILL

To ensure that new mothers and their families are educated about postpartum depression, screened for symptoms, and provided with essential services, and to increase research at the National Institutes of Health on postpartum depression.

Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled,

SECTION 1. SHORT TITLE.

This Act may be cited as the `Mom’s Opportunity to Access Health, Education, Research, and Support for Postpartum Depression Act’ or the `MOTHERS Act’ .

SEC. 2. FINDINGS.

The Congress finds as follows:

(1) Postpartum depression is a devastating mood disorder which strikes many women during and after pregnancy.

(2) Postpartum mood changes are common and can be broken into three subgroups: `baby blues,’ which is an extremely common and the less severe form of postpartum depression; postpartum mood and anxiety disorders, which are more severe than baby blues and can occur during pregnancy and anytime within the first year of the infant’s birth; and postpartum psychosis, which is the most extreme form of postpartum depression and can occur during pregnancy and up to twelve months after delivery.

(3) `Baby blues’ is characterized by mood swings, feelings of being overwhelmed, tearfulness, irritability, poor sleep, mood changes, and a sense of vulnerability that usually starts in the first week and resolves without treatment by the end of the second week postpartum.

(4) The symptoms of postpartum mood and anxiety disorders are as defined in the latest edition of Diagnostic and Statistical Manual of Mental Disorders (DSM), as published by American Psychological Association.

(5) The symptoms of postpartum psychosis include losing touch with reality, distorted thinking, delusions, auditory hallucinations, paranoia, hyperactivity, and rapid speech or mania.

(6) 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.

(7) The causes of postpartum depression are complex and unknown at this time; however, contributing factors include: a steep and rapid drop in hormone levels after childbirth; difficulty during labor or pregnancy; a premature birth; a miscarriage; feeling overwhelmed, uncertain, frustrated or anxious about one’s new role as a mother ; a lack of support from one’s spouse, friends or family; marital strife; stressful events in life such as death of a loved one, financial problems, or physical or mental abuse; a family history of depression or mood disorders; a previous history of major depression or anxiety; or a prior postpartum depression.

(8) Postpartum depression is a treatable disorder if promptly diagnosed by a trained provider and attended to with a personalized regimen of care including social support, therapy, medication, and when necessary hospitalization.

(9) All too often postpartum depression goes undiagnosed or untreated due to the social stigma surrounding depression and mental illness, the romanticization of motherhood, the new mother’s inability to self-diagnose her condition, the new mother’s shame or embarrassment over discussing her depression so near to the birth of her child, the lack of understanding in society and the medical community of the complexity of postpartum depression, and economic pressures placed on hospitals and providers.

(10) Untreated, postpartum depression can lead to further depression, substance abuse, loss of employment, divorce and further social alienation, self-destructive behavior, or even suicide.

(11) Untreated, postpartum depression impacts society through its effect on the infant’s physical and psychological and cognitive development, child abuse, neglect or death of the infant or other siblings, and the disruption of the family.

(12) This Act shares the goals of the Melanie Blocker-Stokes Postpartum Depression Research and Care Act and will help new mothers who are battling with postpartum conditions.

TITLE I–DELIVERY OF SERVICES REGARDING POSTPARTUM DEPRESSION AND PSYCHOSIS

SEC. 101. DELIVERY OF SERVICES REGARDING POSTPARTUM DEPRESSION AND PSYCHOSIS.

Subpart 3 of part B of title V of the Public Health Service Act (42 U.S.C. 290bb-31 et seq.) is amended–

(1) by inserting after the subpart heading the following:

`CHAPTER I–GENERAL PROVISIONS’;

and

(2) by adding at the end thereof the following:

`CHAPTER II–DELIVERY OF SERVICES REGARDING POSTPARTUM DEPRESSION AND PSYCHOSIS

`SEC. 520K. ESTABLISHMENT OF PROGRAM OF GRANTS.

`(a) In General- The Secretary shall in accordance with this chapter make grants to provide for projects for the establishment, operation, and coordination of effective and cost-efficient systems to–

`(1) provide education to women who have recently given birth, and their families, concerning postpartum depression, postpartum mood and anxiety disorders, and postpartum psychosis (referred to in this chapter as `postpartum conditions’) before such women leave their birthing centers and to screen new mothers for postpartum conditions during their first year of postnatal checkup visits, including the standard 6-week postnatal checkup visit; and

`(2) provide for the delivery of essential services to individuals with postpartum conditions and their families.

`(b) Recipients of Grants- A grant under subsection (a) may be made to an entity only if the entity–

`(1) is–

`(A) in the case of a grant to carry out the activities described in subsection (c)(1), a State; and

`(B) in the case of a grant to carry out the activities described in subsection (c)(2), a public or nonprofit private entity, which may include a State or local government; a public or nonprofit private hospital, community-based organization, hospice, ambulatory care facility, community health center, migrant health center, tribal government or territory, or homeless health center; or other appropriate public or nonprofit private entity; and

`(2) submits to the Secretary an application at such time, in such manner, and containing such information as the Secretary may require.

`(c) Certain Activities-

`(1) EDUCATION-

`(A) IN GENERAL- To the extent practicable and appropriate, the Secretary shall ensure that projects under subsection (a)(1) develop policies and procedures to ensure that education concerning postpartum conditions is provided to women in accordance with subparagraph (B), that training programs regarding such education are carried out at health facilities within the State, and that screening and referral is provided in accordance with subparagraph (C).

`(B) REQUIREMENTS- A State that receives a grant or contract under subsection (a)(1) shall ensure that postpartum condition education complies with the following:

`(i) Physicians, certified nurse midwives, certified midwives, nurses, and other licensed health care professionals within the State who provide prenatal and postnatal care to women shall also provide education to women and their families concerning postpartum conditions to promote earlier diagnosis and treatment.

`(ii) All birthing facilities in the State shall provide new mothers and fathers, and other family members as appropriate, with complete information concerning postpartum conditions, including its symptoms, methods of coping with the illness, and treatment resources prior to such mothers leaving the birthing facility after a birth.

`(iii) Physicians, certified nurse midwives, certified midwives, nurses, and other licensed health care professionals within the State who provide prenatal and postnatal care to women shall include fathers and other family members, as appropriate, in both the education and treatment processes to help them better understand the nature and causes of postpartum conditions.

`(C) SCREENING AND REFERRAL- A State that receives a grant or contract under subsection (a)(1) shall ensure that new mothers, during visits to a physician, certified nurse midwife, certified midwife, nurse, or licensed healthcare professional who is licensed or certified by the State, within the first year after the birth of their child, are offered screenings for postpartum conditions by using the Edinburgh Postnatal Depression Scale (EPDS), or other appropriate tests. If the results of such screening provide warning signs for postpartum conditions, the new mother shall be referred to an appropriate mental healthcare provider.

`(D) SUBGRANTS- A State that receives a grant or contract under subsection (a)(1) to carry out activities under this paragraph may award subgrants to entities described in subsection (b)(1)(B) to enable such entities to provide education of this type described in subparagraph (B).

`(2) SERVICES- To the extent practicable and appropriate, the Secretary shall ensure that projects under subsection (a)(2) provide services for the diagnosis and management of postpartum conditions. Activities that the Secretary may authorize for such projects may also include the following:

`(A) Delivering or enhancing outpatient and home-based health and support services, including case management, screening and comprehensive treatment services for individuals with or at risk for postpartum conditions, and delivering or enhancing support services for their families.

`(B) Delivering or enhancing inpatient care management services that ensure the well being of the mother and family and the future development of the infant.

`(C) Improving the quality, availability, and organization of health care and support services (including transportation services, attendant care, homemaker services, day or respite care, and providing counseling on financial assistance and insurance) for individuals with postpartum conditions and support services for their families.

`(d) Integration With Other Programs- To the extent practicable and appropriate, the Secretary shall integrate the program under this title with other grant programs carried out by the Secretary, including the program under section 330.

`SEC. 520L. TECHNICAL ASSISTANCE.

`The Secretary may provide technical assistance to assist entities in complying with the requirements of this chapter in order to make such entities eligible to receive grants under section 520K.

`SEC. 520M. AUTHORIZATION OF APPROPRIATIONS.

`For the purpose of carrying out this chapter, there are authorized to be appropriated such sums as may be necessary for each of the fiscal years 2008 through 2010.’.

TITLE II–RESEARCH ON POSTPARTUM DEPRESSION AND PSYCHOSIS

SEC. 201. CONSENSUS RESEARCH CONFERENCE AND PLAN CONCERNING POSTPARTUM DEPRESSION AND PSYCHOSIS.

Part B of title IV of the Public Health Service Act (42 U.S.C. 284 et seq.) is amended by adding at the end the following:

`SEC. 409J. CONSENSUS RESEARCH CONFERENCE AND PLAN CONCERNING POSTPARTUM DEPRESSION AND PSYCHOSIS.

`(a) Consensus Research Conference and Plan-

`(1) CONFERENCE- The Secretary, acting through the Director of NIH, the Administrator of the Substance Abuse and Mental Health Services Administration, and the heads of other Federal agencies that administer Federal health programs including the Centers for Disease Control and Prevention, shall organize a series of national meetings that are designed to develop a research plan for postpartum depression and psychosis (referred to in this section as `postpartum condition’).

`(2) PLAN- The Secretary, taking into account the findings of the research conference under paragraph (1), shall develop a research plan relating to postpartum conditions. Such plan shall include–

`(A) basic research concerning the etiology and causes of postpartum conditions;

`(B) epidemiological studies to address the frequency and natural history of postpartum conditions and the differences among racial and ethnic groups with respect to such conditions;

`(C) the development of improved diagnostic techniques relating to postpartum conditions; and

`(D) clinical research for the development and evaluation of new treatments for postpartum conditions, including new biological agents.

`(3) REPORT- Not later than 2 years after the date of enactment of this section, the Secretary shall prepare and submit to the appropriate committees of Congress a report concerning the research plan under paragraph (2).

`(b) Activity Relating to Research Plan-

`(1) IN GENERAL- After the development of the research plan under subsection (a)(1), the Secretary, acting through the Director of NIH shall expand and intensify research and related activities of the Institutes relating to postpartum conditions in a manner appropriate to carry out such plan, and in particular shall direct research efforts to carry out such plan.

`(2) REPORT- Not later than 1 year after the development of the research plan under subsection (a)(1), and annually thereafter, the Secretary shall prepare and submit to the appropriate committees of Congress a report on the progress made with respect to such plan and the status of ongoing activities regarding postpartum conditions at the National Institutes of Health.’.

New Jersey First to Require Mercury-Laden Flu Shots

Thursday, December 13th, 2007

On December 11, 2007, outgoing New Jersey Health Commissioner Fred Jacobs gave a gift to Merck, the vaccine and pharmaceutical giant: every pres schooler in New Jersey must receive the flu-enriched shot along with other dangerous vaccines. Parental objections were over ridden by Jacobs who dismissed. Councilwoman Charlotte Vandervalk (R-Bergen) opposed the regulations and has introduced a bill to make exemptions on conviction alone an option for parents. Merck’s Corporate headquarters is in Whitehouse Station, New Jersey.

You can let the Commissioner know how you feel about this by going to the following NJ state link and completing the Comment Form, selecting “General Feedback” in the Program field: http://www.nj.gov/health/feedback.shtml – please be polite…

We’ll also be following these developments through our fellow foundation trustee Ralph Fucetola JD and his blog,
http://vitaminlawyerhealthfreedom.blogspot.com

And you can Take Action here:
http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=21833

———————————————-
Here is the article from the Jersey Journal:

The Jersey Journal
PRE-K FLU VAX
Jersey order to be first some parents oppose it
Tuesday, December 11, 2007
TRENTON – New Jersey moved yesterday toward becoming the first state to require flu shots for preschoolers after a health advisory board backed new vaccine mandates over the opposition of worried parents.
The Public Health Council voted to require New Jersey children attending preschool or licensed day care to get annual flu shots, and to get three additional vaccines for youngsters starting Sept. 1, 2008.
No other state requires preschool, day care or older students to get flu shots, according to the American Academy of Pediatrics.
The state’s health commissioner, Dr. Fred M. Jacobs, has until next Tuesday to sign off on the mandates, though they have already been approved by Gov. Jon S. Corzine. Health Department spokesman Tom Slater said Jacobs was expected sign off on the proposal.
Besides the flu shots, New Jersey also will require preschoolers to get a pneumococcal vaccine and sixth-graders to get a whooping cough booster shot and a meningitis shot.
“Implementation of these rules will save lives and prevent disease and suffering in children, their families and the community,” deputy health commissioner Dr. Eddy Bresnitz told the council yesterday.
The Council voted in favor of the requirements 5-2, with one abstention, with member Dennis San Filippo saying he would like to see studies done on whether it’s safe for young children to get so many doses of different vaccines.
All four vaccines are recommended by the federal Centers for Disease Control and Prevention, the American Academy of Pediatrics and other medical groups.
Parents concerned about possible dangers of the new vaccines and government intrusion in family medical decisions have been trying to block the new shots.
They note that flu vaccines contain trace amounts of mercury, a toxic heavy metal, and that mercury-free shots can be difficult to obtain.
According to the CDC and other scientific groups, there’s no convincing evidence the trace amounts of mercury in flu shots cause harm.
Following the vote yesterday, concerned parents said they will keep urging support for a bill that would give parents a right to a “philosophical objection” to vaccine mandates, as many other states have.
The new vaccines will be available for free for low-income families through the federal Vaccines for Children program, and private insurers generally will cover the cost, Bresnitz said.
———————————

And this is what the Star Ledger reported about Assemblywoman Vandervalk, leading the opposition to forced vaccinations:

“I’m gravely concerned about what’s happening here today,” said Assemblywoman Charlotte Vandervalk (R-Bergen), a sponsor of a bill (A165) that would allow parents to opt out of the vaccine mandates by filing a “conscientious exemption” form with the local health department.

“With New Jersey reporting the highest incidence of autism and a cause yet to be identified, we don’t know what will happen,” she said. “What happened to our freedom?”
——————————–

It is our hope that lots of Jersians and others concerned with this issue will send strong messages of support for Assembly member Vandervalk’s strong, principled stands against the “clout” of Big Pharma. Her bill has been “prefiled” for the new legislature that starts meeting in January. We’ve spoken to her office and she appreciates all the support that can be generated for this bill.

Please check back for updates and new Action Items.

And, of course, we need your generous help to make this possible:
http://www.healthfreedomusa.org/index.php/index.php?page_id=189

———————————————–

UPDATE

The following is a sample of information we’re continually receiving about the Compulsory Vaccination issue and is reprinted here to give you an idea of how important this issue is becoming. With your help, we can magnify our “netroots” (Internet grassroots) impact on public policy. Please make sure you get your friends and email contacts to join the eAlert list at www.healthfreedomusa.org today!

From our DC advocate, Charles Frohman – http://www.cfrohman.com/

1. Alberta Health halts mumps inoculations
Posted by: “C. F.” cfroh@yahoo.com cfroh
Date: Thu Dec 13, 2007 3:37 pm ((PST))

http://www.theglobeandmail.com/
Alberta Health halts mumps inoculations

The Canadian Press
December 12, 2007

Edmonton — Alberta has suspended its campaign to vaccinate young
people against mumps because of severe allergic reactions to the vaccine.

Alberta Health says it is holding off on inoculating 17- to
26-year-olds after five young people with a history of allergies had
bad responses.

All five have recovered.

The campaign was undertaken because of an outbreak of mumps around the
province.
________________________________________________________________________

Maryland Mass Forced Vaccination Update –

2. 700 Maryland parents exposed to jail for nonvaccination
Posted by: “C. F.” cfroh@yahoo.com cfroh
Date: Thu Dec 13, 2007 3:37 pm ((PST))

http://www.washingtonpost.com/

More Students Are Vaccinated

The number of Prince George’s County students who have not met the
state’s immunization requirements dropped by more than half over the
past month after State’s Attorney Glenn F. Ivey (D) threatened
students’ parents with fines and possible jail time, a school system
spokesman said Monday.

Spokesman John White said that 1,084 students had not received a full
program of shots for chicken pox and hepatitis B as of Saturday. This
was a significant improvement over the situation Nov. 13, when Ivey
and school officials sent a letter to the parents of more than 2,300
students warning that they could face a $50 fine for each day they
were out of compliance or up to 10 days in jail.

“The letter certainly got people’s attention,” White said. “It had the
desired effect.”

Many parents reported to free clinics to get their children the
vaccines; others provided proof that they’d gotten the immunizations
in the past. Parents may also request medical and religious exemptions
from the immunization requirement, which the state put into effect in
January.

Of those who have not gotten immunized, White said slightly more than
700 students’ parents — what White called “chronic” cases where there
is no sign that they have made an effort to get immunized or provide
an exemption — have been referred to Ivey’s office for possible legal
action.

Ramon V. Korionoff, a spokesman for Ivey’s office, said last week that
no parents had been fined or jailed.

________________________________________________________________________

3. Merck recalls over 1m doses of children’s vaccine
Posted by: “C. F.” cfroh@yahoo.com cfroh
Date: Thu Dec 13, 2007 3:37 pm ((PST))

Blacklisted News

Merck recalls over 1m doses of children’s vaccine
Published on Thursday, December 13, 2007.

AddThis Social Bookmarking Widget

Source: AP – Media Monarchy

merck recalls over 1m doses of children’s vaccine
More than a million doses of a common vaccine given to babies as young
as two months was being recalled Wednesday because of contamination
risks, but the top U.S. health official said it was not a health threat.

The recall is for 1.2 million doses of the vaccine for Hib, which
protects against meningitis, pneumonia and other serious infections,
and a combination vaccine for Hib and hepatitis B. The vaccine is
recommended for all children under 5 and is usually given in a
three-shot series, starting at two months.

Drug maker Merck & Co., which announced the recall after testing
showed a sterilization problem in a Pennsylvania factory, said
concerned parents should contact their child’s doctor.

“The potential for contamination of any individual vaccine is low,”
said Merck spokeswoman Kelly Dougherty.

Dr. Julie Gerberding, head of the Centers for Disease Control and
Prevention, echoed that in a news conference.

“This is not a health threat in the short run, but it is an
inconvenience,” she said.

________________________________________________________________________

5. Re: Bush Set To Veto To Remove Mercury From Infant Vaccines
Posted by: “Charles D. Frohman” cfroh@yahoo.com cfroh
Date: Thu Dec 13, 2007 3:37 pm ((PST))

Thanks! I blogged about this and would love it if you commented: click
www.CommonInterest.info and scroll down to “pre-holiday threats to liberty”

Jessica Frohman wrote: Since you seemed interested
in the subject and its one I am informed about as well… thought you might be
interested in this…
Bush Set To Veto To Remove Mercury From Infant Vaccines Infant Vaccines

President Bush would veto the HHS-Labor-Education Appropriations Bill because of
the cost and “objectionable provisions” such as a measure to ban the use of
childhood flu vaccines that contain thimerosal, a mercury-based preservative.

Autism advocacy groups are outraged because President Bush stated in a
questionnaire during his 2004 campaign: “I support the removal of Thimerosal
from vaccines on the childhood national vaccine schedule. During a second term
as President, I will continue to support increased funding to support a wide
variety of research initiatives aimed at seeking definitive causes and/or
triggers of autism. It is important to note that while there are many possible
theories about causes or triggers of autism, no one material has been definitely
included or excluded.”

But since 2005, President Bush has steadfastly refused to issue an Executive
Order banning high amounts of mercury in vaccines that would protect children
and pregnant women despite repeated requests from the autism community that he
uphold his campaign promise. Under his current administration, mercury has been
and will continue to be knowingly injected into the youngest of American
citizens. The controversial mercury-containing preservative thimerosal has been
linked by thousands of parents as being the cause of their children’s mercury
poisoning and autism.

The flu vaccine which continues to be manufactured with mercury is recommended
for all pregnant women, infants and children despite the fact that the Institute
of Medicine in 2001 recommended against the policy of exposing these same
sensitive groups to thimerosal containing vaccines. According to the EPA, one in
every six women of childbearing age already has blood levels of mercury high
enough to cause neurological damage to their unborn children due to
environmental exposures alone.

“Injecting even more mercury into the bodies of pregnant women, infants and
children when it is not a necessary component of vaccines is just bad medicine,”
said Lyn Redwood, president of SafeMinds and parent of a mercury-injured child.
“It defies logic that a flu vaccine must be disposed of as a hazardous waste if
it is not used, but somehow injecting the same mercury-containing vaccine into a
baby is safe.”

Charles D. Frohman
202-536-4346 (office)/202-258-8027 (mobile)
________________________________________________________________________
6. Vaccine Politics
Posted by: “C. F.” cfroh@yahoo.com cfroh
Date: Thu Dec 13, 2007 3:37 pm ((PST))

http://infowars.net/articles/december2007/131207Vaccine.htm

Vaccine Politics

Rick Fisk
Lew Rockwell.com
Thursday December 13, 2007

The first vaccine mandated by governments was the small pox vaccine.
Today, you’ll hear any number of medical professionals refer to the
vaccine as proof of Western military medicine’s superiority over any
other discipline. The World Health Organization proclaims proudly to
anyone who will listen that the vaccine has eradicated smallpox (yet
for a disease “indistinguishable from smallpox,” apply the same
vaccine used to protect against smallpox).

So prevalent is the favorable view of vaccines, that people who
question this “truism” are ridiculed. But, when the vaccine had been
about 100 years old (it is now over 200 years old), it had its
detractors. One of them was a scientist, Alfred Russel Wallace.

Wallace was an interesting man. His list of accomplishments is
stunning. Sometimes referred to in England as the “Grand Old Man of
Science,” he continued to produce papers into his 90s. A reluctant
socialist, he felt that science and government didn’t mix and had no
problem arguing against government involvement in science.

Wallace focused on biology and zoology in his early career and turned
to social issues later in life. One such social issue was vaccination.
He noted in 1906 that doctors were not the best judges of a vaccine’s
efficacy though they were continuously consulted on vaccination policy
by government officials.

In the first place they are interested parties, both pecuniarily
and in a much greater degree on account of professional training and
prestige. Only three years after vaccination was first introduced, on
the recommendation of the heads of the profession, and their expressed
conviction that it would give lifelong protection against a terrible
disease, Parliament voted Jenner [the scientist who created the
smallpox vaccine derived from cowpox] £10,000 in 1802, and £20,000
more in 1807, besides endowing vaccination with £3,000 a year in 1808.
From that time doctors as a body were committed to its support; it has
been taught for nearly a century as an almost infallible remedy in all
our medical schools; and has been for the most part accepted by the
public and the legislature as if it were a well-established scientific
principle, instead of being as the historian of epidemic diseases –
Dr. Creighton – well terms it, a grotesque superstition.

This quote is from a summary of his original arguments against
mandatory use of the smallpox vaccine in 1889: Vaccination: Proved
Useless & Dangerous. (Wallace wasn’t one for mincing words.) The 1889
work was an epidemiological study which showed that smallpox rates in
London and the rest of England were not reduced at all by the
mandatory use of the vaccine. In fact, other illnesses increased
during the time that the smallpox vaccination was forced on the
population suggesting that the effect on immunity was negative rather
than positive as vaccination proponents kept asserting.

The 1889 study was instrumental in influencing public opinion and
ultimately forcing the repeal of laws making smallpox vaccination
mandatory in England. Other European nations followed suit. The U.S.
government’s medical and scientific organizations and the World Health
Organization have disregarded Wallace’s findings, as well as a long
list of subsequent papers and corroborations, and have proclaimed that
the smallpox vaccine was a smashing success.

This has occurred, in spite of the fact that there have been no
counter-examples to disprove the contrary view. There have been many
examples since which tend to support Wallace’s conclusions however.

For instance, one of the most stunning antidotes to the idea that
smallpox was eradicated due to mandatory vaccination is the Japanese
example. The practice of “revaccination” was prevalent there (and in
the British Navy) until their vaccination rate exceeded 100%! In spite
of this, Japan faced huge smallpox epidemics. All told, the Japanese
lost 48,000 people to smallpox, most of them vaccinated at least once.
When the government stopped the mandatory vaccinations, the epidemics
were finally arrested. Were the smallpox vaccination truly effective
as a prophylactic, such an example could not exist. Unfortunately,
there are dozens just like it all over the world.

In 1904, the U.S. Army decided to forcibly vaccinate the Philippine
population ostensibly to improve health conditions but more likely
intended to protect military personnel. They touted its success when
in the following two years smallpox appeared to be under control.
However, from 1917 to 1919, in a population of 11 million that had a
reported 100% vaccination rate, smallpox epidemics claimed over 70,000
lives out of 163,000 reported infections.

By contrast, Australia, from 1900 to 1915, which never instituted a
mandatory vaccine program, reported 3 deaths due to smallpox over the
entire period.

A doctor who treated smallpox victims in San Antonio near the turn of
the century wrote of his experiences. Charles Campbell became so
trusted by his patients and coworkers that they agreed to allow him to
expose them to smallpox to help him prove his own theories about how
smallpox was transmitted, treated and how its effects could be minimized.

Only one of his patients received the pock marks so customarily
associated with the disease and that patient’s pock marks were “done
intentionally.” Dr. Campbell’s belief, based on his observations and
experience, was that smallpox was spread by bed bugs, a pest most of
us haven’t had to experience in our lifetimes but is making a
comeback. That the bed bug could be a vector makes logical sense given
what we know about the spread of smallpox to Native American
populations via blanket distributions. Viruses do not live for long
periods of time absent a host; unlike bacteria which can lay dormant
for decades while retaining viability. Bed bugs, like fleas, offer a
convenient host for a virus and can live for weeks without food in
unwashed bedding. Campbell’s work has been mostly ignored by the
establishment medical community and the press.

Why haven’t Campbell’s experiences, treatment results and the general
knowledge of the smallpox vaccine’s danger been more prevalent instead
of the current view that vaccines are a modern miracle?

This puzzling contradiction doesn’t just apply to the smallpox
vaccine. We’re told that polio’s low current rate of infection is due
to the vaccine. However, a closer look tends to discredit that idea as
well. Those who track world health statistics do not consider
vaccination as having reduced disease rates by any more than 3%
world-wide during the 19th and 20th centuries. The reduction in
infectious disease has been attributed to sanitary improvements or
natural immunity and natural disease cycles, not vaccination.
Furthermore, since 1970, there have been no cases of polio in the U.S.
which are not attributed to the vaccine itself.

In spite of the overwhelming evidence against the benefits of
vaccination, our own government health officials continue to recommend
a growing battery of vaccinations, starting with infants at birth. The
CDC’s recommended vaccination schedule(pdf) is staggering compared to
what it was just 20 years ago. If you strictly followed the CDC’s
recommendations, your child would have twenty-five vaccine injections
by the time they reached four years of age. What justifies such a number?

To be fair, the growing list of vaccinations is suggestive rather than
mandatory. That being said, there are government officials who use
these suggestions to augment the list of “mandatory” vaccinations that
children must have before attending public school. Think about that
for a second. How are state school boards qualified to mandate
vaccination schedules?

Doubts over the efficacy of vaccines appear to be increasing as
information has been made available. Until the internet, many of the
contrary studies were not available to the general public. We are only
recently discovering that what we’re told by our own government
agencies and the drug companies they appear to represent, are not
exactly representative of the facts.

The list of additives and basic ingredients found in many vaccines
would be otherwise advised against by ethical medical professionals,
but we are told repeatedly by our own FDA that there is no evidence to
suggest that injecting mercury (thimerosal) and other additives
directly into the bloodstream is harmful. Meanwhile, the EPA will send
in armed police to shut down somebody’s private business as an
immanent threat to the population if some bureaucrat happened to
detect mercury on or about the premises.

Why the disparity? Quite frankly, it is because the corporations who
create the vaccines have gained control over our regulatory agencies
and legislative bodies. The FDA’s regulations have been continuously
augmented internally and by Congress to protect pharmaceutical
companies from litigations. The Vaccine Adverse Effects Reporting
System has been put in place to protect the public, but is really a
way to protect the drug companies from lawsuits.

Apathy and lack of confidence in ourselves has led to an irrational
reliance upon government experts employed by the, FDA, CDC and WHO to
inform us about the causes of disease and to control how our
government responds to health crises. That is a lot of power
concentrated in one place.

What has resulted from this unholy marriage of corporate interests and
the government is not public health but political medicine. Both
figuratively and literally, political medicine is poison that seeks to
destroy common sense, customer choice and too often, lives. When it
isn’t denying medication that has been proven useful to cancer
patients, it is attempting to mandate medicine and ban food supplements.

If one didn’t know any better, one might conclude that the FDA and
related health agencies of the federal government, want you to get sick.

________________________________________________________________________

And from Dr. Rebecca Carley –

Soldiers being trained to give immunizations to base civilians
http://www.stripes.com/article.asp?section=104&article=50931

By Jimmy Norris, Stars and Stripes
Pacific edition, Thursday December 13, 2007

YONGSAN GARRISON, South Korea — With even more family members on the way to
South Korea as part of the transformation of U.S. forces on the peninsula, the
18th Medical Command had some good news for those who will be seeking
immunizations.

Thanks to a team of instructors from Walter Reed Army Medical Center in
Washington, 19 more 18th Medical Command soldiers will be qualified Friday to
administer immunizations to civilians.

The instructor team was in South Korea to give a five-day immunology course to
medics.

Prior to the course, the medics were qualified to give immunizations only to
active-duty soldiers. The five days of training are normally part of Walter
Reed’s 5½-week immunization and allergy technician course.

But the cost and loss of manpower involved in sending them on temporary duty
for that training would not have been practical, said Master Sgt. Desmond Smith,
18th Medical Command spokesman.

“It’s easier to bring someone here than to send 19 soldiers to the States,”
he said.

The visiting instructors did not cover the allergy portion of the 5½-week
course, so students will not receive what the Army calls an additional skill
identifier. They will, however, receive a certificate of completion for their
training and a memorandum verifying they have completed the training necessary
to give immunizations to children.

“There was clearly a need at 121 [Combat Support Hospital] to increase the
number of people who could give pediatric immunizations,” said Maj. Cecilia
Mikita, who led the team from Walter Reed.

The training covered 20 types of immunizations and six ways to administer them.
It also included lectures on record keeping, the effects of various vaccines on
the body, and the proper handling and storage of vaccines.

Included in the hands-on portion of the course were stations at the hospitalÂ’s
pediatric immunization clinic, 1st Replacement CenterÂ’s medical in-processing
area, and Yongsan GarrisonÂ’s Troop Medical Clinic.

“A lot of stuff I learned on the job, but this course gives you a real
standard,” said student Pfc. David Dasilma. “I can educate my patients now and
tell them why they need a shot and what it does to their body.”

Smith said the training should lead to a decrease in wait times at immunization
clinics.

“It helps because if you come in for a shot there’s more than one person
available to give it now,” he said.

Dr. Carley Responds:

The idea that a 5 day course could prepare anyone to handle the consequences of
inoculations (which include anaphylactic shock and death) is insane. Worse yet,
“The visiting instructors did not cover the allergy portion”. As is explained
in my documents on www.drcarley.com, the corruption of the immune system caused
by inoculations with disease is what causes allergies, as well as all autoimmune
diseases and cancer.

This is the beginning: soldiers will now be shooting diseases, as well as
bullets. As you all know from the MSNBC links on my site, the bird flu vaccine
has already been licensed. The model state health emergency powers act gives
the governors of every state the authority to order inoculations be given to
citizens. The bird flu vaccine will cause the bird flu pandemic, which will
give the traitor in the white house an excuse to proclaim martial law. One of
his executive orders gives him the power to cancel the 2008 election in the case
of such a situation.

I tell you this not to scare you, but prepare you. Each of you must decide what
you will do when the knock comes on the door and you are ordered to take the
bird flu vaccine. The only way this can be stopped is to wake up enough people
that the plan does not work due to mass refusal, as occurred a couple of years
ago when Bush wanted all health workers to be inoculated with smallpox.

I ask each of you to send your own lists this e-mail, so they can send it out to
theirs, and so on. Let the truth spread like a virus, so the obvious plan is
not successful. There is nothing to fear but fear itself…the truth will set
us free. I do not believe this; I KNOW it.

Let’s roll….

Dr. Carley

Dr. Rebecca Carley
http://www.drcarley.com

*** Dr. Carley’s information is not intended to diagnose, treat or cure any
diseases. Rather, it is for educational purposes only. ***