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Fluoridated Water: Drugging Without Your Consent

By Dr. Mercola

Most people are aware that you should not swallow your toothpaste, and many even know this is because of the fluoride it contains. But when it comes to fluoride in drinking water, many are either unaware that it is there, or they trust their government to know―and do―what’s best for them.

Detox Protocol

Many therefore assume that if the government allows fluoride in their water, it must be safe – but it’s not.

    There is an abundance of information available on the devastating health effects of fluoride. If this is news to you, the video above may be hard to swallow (as we hope the fluoride will be, following you viewing it) … but it’s truth that needs to get out.

You’re Being Drugged Without Your Consent

    Assuming you live in an area that fluoridates water, and you drink from the municipal water supply, you’re being exposed to a toxic drug-like substance every time you take a sip. Fluoridating water is reckless, as you cannot control the dose ingested, or who receives it, and there’s no medical supervision. Water fluoridation clearly violates your right to informed consent as far as medical decisions go.

    There is not a single process in your body that requires fluoride, but swallowing this toxin has been found to damage your soft tissues (brain, kidneys, and endocrine system), as well as teeth (dental fluorosis) and bones (skeletal fluorosis). There are more than 100 published studies illustrating fluoride's harm to your brain, plus 25 published studies directly linking fluoride exposure to reduced IQ in children!i

    Dr. Bill Osmunson, an avid supporter of fluoride opposition, states:

        "No one fixes IQ. This is an irreparable, irreversible damage that's happening to our public. When you look at the bell curve of human distribution of intelligence, at the very bottom, way down there at the end, is what we scientifically call the mentally retarded. When you skew IQ five points down, that means that you're doubling the number of mentally retarded and you're halving the number of gifted and everybody else moves on down."

    In a nutshell, everyone drinking fluoridated water on a regular basis is getting less intelligent across the board …

    It’s also known that over time fluoride accumulates in many areas of your body, including areas of your brain that control and alter behavior, particularly your pineal gland, hippocampus and other limbic areas. One particularly striking animal study published in 1995ii showed that fluoride ingestion had a profound influence on the animals' brains and altered behavior. Pregnant rats given fluoride produced hyperactive offspring. And animals given fluoride after birth became apathetic, lethargic "couch potatoes."

Did You Know Drinking Fluoride Isn’t Even Good for Your Teeth?

    Even if you were willing to risk brain damage and even cancer from drinking so much fluoride, in the event it might spare your teeth from decay … you need to know that systemic fluoride has not been shown to reduce cavities. The early historic studies on fluoridation found that naturally-occurring fluoride also happens to be found in areas that are high in calcium and other minerals. According to Dr. Osmunson, many dentists at the time theorized that this higher mineral content might be the real reason for the reduction in tooth decay.

    There were some compelling studies showing that fluoride made teeth harder and more able to withstand acids. However, upon further review of the research literature, Dr. Osmunson realized that the evidence supporting fluoride really wasn't as strong as initially touted, and fluoride did not appear to reduce tooth decay to any significant degree.

    In fact, he discovered plenty of scientific evidence showing that areas with LESS fluoride had less decay.

    A recent review of 11 studies involving more than 7,000 children likewise showed that the effect of fluoride supplements on primary teeth could not be determined, with one study showing no cavity-reducing effect.iii Meanwhile, the study revealed the supplements have only dubious cavity-reducing effects on permanent teeth, and no difference was noted between fluoride supplements or topical fluoride for preventing cavities.

You’re Drinking a Toxic Industrial Waste Product

    Even if you’re already aware that fluoride is in your drinking water, you might not realize that it is not the naturally-occurring variety. It’s not even pharmaceutical grade.

    It's a toxic industrial waste product, which is also contaminated with lead, arsenic, radionucleotides, aluminum and other industrial contaminants, and even worse if your municipality is foolish enough to purchase it from China.

    The story gets even more convoluted, as declassified files of the Manhattan Project and the Atomic Energy Commission show that the original motivation for promoting fluoride and water fluoridation in the United States was to protect the bomb- and aluminum- and other fluoride-polluting industries from liability. In the early days some of the sodium fluoride used to fluoridate water supplies in the U.S. came from Alcoa.

    A couple of years later, they switched to the even more hazardous waste product hydrofluorosilicic acid from the phosphate fertilizer industry. But none of the studies on fluoride actually used the far more toxic and contaminated hydrofluorosilicic acid that is added to the water supply. Rather, they use pharmaceutical-grade fluoride, which while harmful, is not quite as bad as what's being used for water fluoridation. So, the health hazards are likely FAR worse than any study has so far discerned.

    One early sign of over-exposure to fluoride is dental fluorosis, which typically begins as white specks on your teeth, which then progress to more unsightly yellow and brown mottling of the enamel. At the first signs of dental fluorosis, if you haven't done so already, you'll want to immediately eliminate as many sources of fluoride as possible. Shockingly, 41% of adolescents in the US currently have dental fluorosis from overexposure to fluoride. And remember nearly one-third of the US is NOT fluoridated.

Can You Remove Fluoride From Your Drinking Water?

    Fluoride currently contaminates nearly 70 percent of the U.S. public water supplies. Therefore, it is an extreme challenge to limit your exposure even inside the safety of your own home. For people living in areas with fluoridated tap water, fluoride is a part of every glass of water, every bath and shower, and every meal cooked using that water.

    You could opt for bottled water, but as a general rule, I don't recommend or encourage using bottled water on a regular basis—for a number of reasons. Not only does it contribute to profound amounts of environmental pollution, but a variety of toxins can leach from the plastic, contaminating your water. Not to mention the fact that you're not guaranteed a more pure product to begin with.

    An estimated 40 percent of all bottled water is just bottled tap water that may or may not have received additional water treatment. In fact many bottles waters actually believe fluoride is useful to they add it back in the water! And many others just use filters that do not remove fluoride. So buying bottled water certainly is not a guarantee of getting either pure or fluoride-free water!

    For pure drinking water, your best bet, from a practical perspective, is to filter the water coming into your own home. Unfortunately, fluoride can be quite difficult to remove from water once added in. Reverse osmosis systems have typically been recommended to remove fluoride, but according to fluoride activist Jeff Green, many home systems may not be very efficient at this task. Commercial systems are typically much better, as they have redundancy features not found in smaller-scale residential models.

    So while you can easily choose not to take fluoride supplements or opt to buy fluoride-free toothpaste and mouthwash, you're stuck with whatever your community puts in the water, and it's very difficult to filter out of your water once it's added. Many do not have the resources or the knowledge to do so.

    The only real solution is to stop the archaic practice of water fluoridation at the source and become a fluoride-free activist. However this does not mean showing up to your local municipal meetings and lecturing them about the dangers of fluoride. That approach rarely works.

What’s the Best Strategy to Get Fluoride Out of Drinking Water for Good?

    A far more effective strategy is to find a champion already on the city council and mentor that person to do their own due diligence, which will eventually allow them to “discover” the truth themselves — far more effective and far more likely to resist overturning the decision in a future administration.

    I recently interviewed Jeff Green, who has been an activist in the movement to eliminate toxic fluoride from your water supply for the past 15 years. One element he addressed is that many of us who are first exposed to issues such as this enter into a world of anger at injustice, where we see the problem so passionately and so clearly that we carry the burden of truth and are in a hurry to tell others to set it right, viewing anyone who does not immediately agree with our view as opposition that must be overwhelmed with facts and a list of "shoulds."

    In this state we look angry, and are easily characterized as a zealot, probably because we are. Asking someone without our passion to join us may not be that inviting.

    Should we expect that this would be any different when speaking to authorities and asking them to act? If you are able to suspend your anger at injustice, able to switch your focus from stating the problem to addressing solutions, there are avenues available. If you would like to elevate your discussions from the argumentative "he said, she said" to letting the facts declare themselves, and you are in a position of authority from which you can champion the performance of due diligence, contact us for access to guidance and further information.

    If you are capable of being an advocate of safe drinking water and would like to assist in identifying a champion for due diligence in your community, contact us for approaches and further information.

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CDC and Friends Sprinting Towards the Polio Finish Line

by Suzanne Humphries

The CDC announced on June 8th that they are almost at the finish line of global polio eradication. They’ve not had a case of wild polio since January 13, 2011. Whoopee! But they still have plenty of paralysis. In fact they have more and more every year. AND …children with non-polio Acute Flaccid Paralysis (AFP), the new name for polio, are at more than twice the risk of dying than those with wild polio infection! In fact, more oral polio vaccine has correlated strongly with "non-polio" AFP. One must wonder what exactly the WHO, UNICEF, Rotary International and the Bill and Melinda Gates Foundation are really going for.

Vaccine Protocol

Many believe that a disease called "polio" has been eradicated in the Western hemisphere. Most everyone thinks that "polio" was eradicated by vaccination. To fully understand where polio went, one must understand what polio was. When one understands what polio was, it becomes clear that it is impossible to eradicate it with a vaccine. But that never stops vaccination interests from launching full- scale propaganda misinformation campaigns in order to vaccinate the children of the world, even though they fail in eliminating paralysis. "Wild" poliovirus may be gone from vaccinated countries, but what was once called "polio," and frightened the wits out of parents world-wide, is still ubiquitous.

The term "poliomyelitis" is a description of spinal pathology. The meaning of the word comes from Greek:

polios= gray, and muelos =marrow, itis=inflammation; meaning "inflammation of the gray matter of the spinal cord."

All poliomyelitis means is that the gray matter of the spinal cord is inflamed. This can occur anywhere from the brainstem to the end of the spinal cord, and it has always had many causes, the least of which is a virus that lives in intestines of healthy people.

The result of this inflammation, whether chemical or viral, leads to certain characteristic muscular symptoms that have been conditioned into the minds of several generations of people to appear as the classic atrophied limbs, iron lungs and other horrifying images.

By definition and by historical documentation, these infamous images of polio should by no means be blamed solely on a specific wild-type (naturally occurring) virus. Environmental toxins, other infections, and laboratory-derived vaccine viruses were all implicated in paralytic polio over the years. Yet wild virus, even though it is said to be asymptomatic in 95% of infected, and only causes paralysis in a small amount of infected is the excuse for world-wide polio vaccination with live viruses that are known to cause their own outbreaks of polio in China, Nigeria and India.

Polio Morbidity

"Approximately 95% of persons infected with polio will have no symptoms. About 4-8% of infected persons have minor symptoms, such as fever, fatigue, nausea, headache, flu-like symptoms, stiffness in the neck and back, and pain in the limbs, which often resolve completely. Fewer than 1% of polio cases result in permanent paralysis of the limbs (usually the legs). Of those paralyzed, 5-10%[of that 1%] die when the paralysis strikes the respiratory muscles."[1]

Naturally existing polio is thought to have been a normal bowel commensal for hundreds of years before paralytic polio emerged as an epidemic disease, beginning in white populations. For instance, an in-depth study of a remote Indian tribe in the Rio das Mortes in the State of Mato Grosso, Brazil demonstrated the presence of the virus with consistent and high levels of immunity – and no disease.

"The paradox of a virtual absence of paralytic poliomyelitis among such heavily infected groups as this, despite high antibody titers, is well known, but the interpretation of the observation remains under discussion. "[2]

Native populations are known to have harbored polioviruses of all three strains with no poliomyelitis whatsoever.

"…the tests recorded in the table, studies of antibody avidity according to the techniques of Sabin (1957) were made on six randomly selected specimens. All six specimens were positive for antibodies to all three types of poliomyelitis, providing additional confirmation of the validity of the findings."[3]

Any thinking person would have to wonder what changed to make the natives and the non-natives become paralyzed from an otherwise completely innocent viral bowel commensal. Dr Loyd Aycock, in 1942 said "

"…frank disease among those exposed to the virus is not only greatly limited but exhibits selectivities which indicate that some added circumstance enters into the determination of whether clinical or subclinical disease results upon exposure to the virus."[4]

This statement was prophetic and unfortunately largely ignored. Some of the "added circumstances" that are known by polio scientists and well documented in medical literature to be highly correlated with paralytic forms of polio include tonsillectomy, intramuscular injections of any sort, vaccines, DDT, arsenic, misdiagnosed syphilis, coxsackie virus, other enteroviruses just to name a few.

Tonsillectomy was at its peak in 1959 at 1.4 million surgeries and declined drastically in years following. DDT was outlawed in the USA but is still found all over India. Arsenic is no longer commonly used as an intramuscular injection up to 100 times in a single person to treat syphilis like it was in the 1940’s – but there is an abundance of unnecessary intramuscular injections in India. Differential diagnoses now exist for paralysis unlike the old days of polio epidemics before the hailed Salk vaccine came to be, when all that became numb or transiently paralyzed was "polio."

History is about to repeat itself in India, Pakistan, and Nigeria. In the USA there was a similar campaign and renaming- after the vaccine was accepted- just like occurs today in India. During a Detroit epidemic in 1958, four years into the Salk vaccine campaign, it was determined that nearly half of the cases of "polio" were not poliovirus-associated and were given other designations than polio.

"During an epidemic of poliomyelitis in Michigan in 1958, virological and serologic studies were carried out with specimens from 1,060 patients. Fecal specimens from 869 patients yielded no virus in 401 cases, poliovirus in 292, ECHO (enteric cytopathogenic human orphan) virus in 100, Coxsackie virus in 73, and unidentified virus in 3 cases. Serums from 191 patients from whom no fecal specimens were obtainable showed no antibody changes in 123 cases but did show changes diagnostic for poliovirus in 48, ECHO viruses in 14, and Coxsackie virus in 6. In a large number of paralytic as well as nonparalytic patients poliovirus was not the cause. Frequency studies showed that there were no obvious clinical differences among infections with Coxsackie, ECHO, and poliomyelitis viruses. Coxsackie and ECHO viruses were responsible for more cases of "nonparalytic poliomyelitis" and "aseptic meningitis" than was poliovirus itself."[5]

Today in India, "polio" is a well-publicized problem, and DDT can be found on the shelves just about everywhere. India is the only country that still manufactures DDT, and remains the chemical’s largest consumer.

DDT enhances the release and intracellular multiplication of poliovirus.[6] Thus it likely contributes to creating a monster out of a normally benign gut virus. Additionally, exposure to DDT induces symptoms that can be completely indistinguishable from poliomyelitis – even in the absence of a virus.[7] Here is a description of DDT poisoning, which is indistinguishable clinically from poliomyelitis.

"Acute gastroenteritis occurs, with nausea, vomiting, abdominal pain, and diarrhea usually associated with extreme tenesmus. Coryza, cough and persistent sore throat are common, often followed by a persistent or recurrent feeling of constriction or a "lump" in the throat; occasionally the sensation of constriction extends substernally and to the back and may be associated with severe pain in either arm. Pain in the joints, generalized muscle weakness, apprehension and exhausting fatigue are usual; the latter are often so severe in the acute stage as to be described by some patients as "paralysis."[8]

Despite the known dangers of oral polio vaccines, that paralysis is on the rise, and that many other entities enhance the virulence of poliovirus, multi-billion dollar polio eradication campaigns march on, often vaccinating a single child 15 times (or more) with live vaccine by their 5th year of life.

"In fact, at the end of 2005, children under 5 years old were reported to have received on average 15 doses of tOPV in UP and Bihar, compared with 10 in the rest of India, and only 4% of children were reported to have received fewer than 3 doses, of whom 90% were under 6 months old… this level of vaccine coverage should have eliminated infection."[9]

It didn’t eliminate infection, and in fact more oral polio vaccine has correlated strongly with "non-polio acute flaccid paralysis." The response by WHO and GAVI is to ramp up the current oral polio vaccination campaigns in recent years. Now some children are reported to have received 32 vaccines in one day.

"At a vaccinators’ meeting in Sultangunj Referral Hospital held Tuesday, supervisors reported a "new" resistance coming from the "educated middle class people" who were getting tired of several rounds of immunisation: one family claimed that their five year old child had received pulse polio vaccination 32 times."[10]

Here is a picture of what is happening in India, the country that hasn’t had a polio case since January 13, 2011:

Rise of Acute Flaccid Polio Paralysis

In India today, as the World Health Organization tracks polio during the vaccination campaigns, it seems that "polio" has declined while "acute flaccid paralysis" (AFP) has increased annually, reaching 60,000 new cases in 2011.
The causes of AFP that have been identified are as follows:

Poliomyelitis, Non-polio enterovirus, vaccine-associated poliomyelitis(not counted as polio), Rabies virus, Varicella zoster virus, Japanese encephalitis virus, Guillain-Barre syndrome, Cytomegalovirus, sciatic neuritis from injection, Transverse myelitis, epidural abscess, spinal cord compression, exotoxin of Corynebacterium diptheriae, toxin of Clostridium botulinum, Karwinskia, tick bite paralysis, Lyme borreliosis, Myasthenia gravis, polymyositis autoimmune, viral myositis, trichinosis, toxic myopathies among others.[11]

As a result of the unrelenting OPV campaigns in India, there has been an exponential rise in "acute flaccid paralysis" while the number of documented cases of "polio" has declined."

"It has been reported in the Lancet that the incidence of AFP, especially non-polio AFP has increased exponentially in India after a high potency polio vaccine was introduced… Sathyamala examined data from the following year and showed that children who were identified with non-polio AFP were at more than twice the risk of dying than those with wild polio infectionnon-polio AFP rate increases in proportion to the number of polio vaccine doses received in each area… Nationally, the non-polio AFP rate is now 12 times higher than expected. In the states of Uttar Pradesh (UP) and Bihar, which have pulse polio rounds nearly every month, the non-polio AFP rate is 25- and 35-fold higher than the international norms… The non-polio AFP rate during the year best correlates to the cumulative doses received in the previous three years…. Association of the non-polio AFP rate with OPV doses received in 2009 was 41.9%. Adding up doses received from 2007 increased the association (R2 = 55.6% p < 0.001)."[12]

Image may be subject to copyright

What is clear from the above graph is that massive "pulse" vaccination campaigns have done nothing to eliminate paralysis, and in fact there is evidence pointing to the likelihood that vaccination is related to the rise in AFP. Isn’t the vaccination really about eliminating paralysis…or is it simply to replace wild virus with a vaccine virus no matter the outcome?

Why doesn’t the World Health Organization notice the medical literature that points to the truth that paralysis has increased with pulse vaccination campaigns in India? How could they possibly explain the intensification of a failed and harmful vaccine campaign where a deadly form of non-polio AFP increases exponentially in children heavily vaccinated with oral polio vaccines?

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Despite Exuberance Many Vaccines Do Far More Harm Than Good

by Sayer Ji, founder

If you visit the World Health Organization’s website, or that of the Centers for Disease Control and Prevention, the information presented there on vaccines is so clearly one-dimensional, repeating the age-old pro-vaccine mantra: "safe"—"effective"—"safe"—"effective" ad nauseam, that before long, you either become lulled into complacency, or stray off into less officially sanctioned sources of information, such as the many anti-vaccine sites on the internet, where discussion of the abject failure of vaccines repeats the same mantra, but recorded backwards like a Beatles record: "unsafe"—"ineffective"—"unsafe"—"ineffective."  

Vaccine Protocol

So, where should one go for the absolute truth on the matter?

According to the dominant medical system, as represented by organizations like the CDC, FDA and WHO, peer-reviewed and published research is the holy grail, without which, claims against vaccines are merely anecdotal, superstitious and/or irrational polemic.  

But, what happens when published scientific research freely available on the National Library of Medicine’s public domain bibliographic database known as Medline, contradicts the pro-vaccine party line?  

A recent review published in April in the journal Expert Review of Vaccines titled, "Review of the risks and benefits of yellow fever vaccination including some new analyses," revealed a surprising fact about yellow fever vaccines:  

From 1990 to the present, the number of cases (n = 31) and deaths (n = 12) from YEL-AVD [attenuated yellow fever vaccine]  in travelers has exceeded the reports of YF [wild-type yellow fever] (n = 6) acquired by natural infection, raising the question whether the risk of vaccination exceeds the benefit in travelers.1

Say what?

So, according to this review, if you add up the net harm done by yellow fever vaccines over the past 22 years of their tracked use in travelers versus their net good, your chance of getting sick from the vaccine is 5 times higher, and getting killed at least 12 times higher, than taking your chances unvaccinated.

While surprising, this is not the only case where a so-called "vaccine-preventable diseases" has been found to be less destructive than the vaccines being used to "prevent" them. Increasingly, the truth about vaccine-induced injuries and death are coming to light through the very organizations and research institutions that have championed their use, and fashioned their image into modern medicine’s most successful technological innovation against infectious disease. 

Case in point…

Polio Vaccines Paralysis

The Polio Global Eradication Initiative (PGEI), founded in 1988 by the World Health Organization, Rotary International, UNICEF, and the U.S. Centers for Disease Control and Prevention, holds up India as a prime example of its success at eradicating polio, stating on its website (Jan. 11 2012) that "India has made unprecedented progress against polio in the last two years and on 13 January, 2012, India will reach a major milestone – a 12-month period without any case of polio being recorded."

This report, however, is highly misleading, as an estimated 100-180 Indian children are diagnosed with vaccine-associated polio paralysis (VAPP) each year. In fact, the clinical presentation of the disease, including paralysis, caused by VAPP is indistinguishable from that caused by wild polioviruses, making the PGEI's pronouncements all the more suspect.2

According to the Polio Global Eradication Initiative's own statistics3 there were 42 cases of wild-type polio (WPV) reported in India in 2010, indicating that vaccine-induced cases of polio paralysis (100-180 annually) outnumber wild-type cases by a factor of 3-4. Even if we put aside the important question of whether or not the PGEI is accurately differentiating between wild and vaccine-associated polio cases in their statistics, we still must ask ourselves: should not the real-world effects of immunization, both good and bad, be included in PGEI's measurement of success?

For the dozens of Indian children who develop vaccine-induced paralysis every year, the PGEI's recent declaration of India as nearing "polio free" status, is not only disingenuous, but could be considered an attempt to minimize their obvious liability in having transformed polio from a natural disease vector into a manmade (iatrogenic) one.

VAPP is, in fact, the predominant form of the disease in developed countries like the US since 1973.4 The problem of vaccine-induced polio paralysis was so severe that the The United States moved to the inactivated poliovirus vaccine (IPV) in 2000, after the Advisory Committee on Immunization Practices (ACIP) recommended altogether eliminating the live-virus oral polio vaccine (OPV), which is still used throughout the third world, despite the known risks.

Things, however, may be be far worse than reported…

A highly concerning paper published in the April-June issue of the Indian Journal of Medical Ethics discusses the possibility that the 47,500 new cases of "non-polio acute flaccid paralysis (NPAFP)" in children reported in 2011, which is clinically indistinguishable from polio paralysis but twice as deadly, were directly proportional [i.e. casually linked] to doses of oral polio received.  According to the authors of this paper: "Though this data was collected within the polio surveillance system, it was not investigated. The principle of primum-non-nocere [First, do no harm] was violated." In other words, instead of acknowledging the high prevalence of vaccine-associated polio paralysis (VAPP), those administering the vaccines and doing surveillance on adverse events simply reclassified the symptoms of injury from polio vaccine to non-vaccine related by coining a new disease terminology, i.e. "non-polio acute flaccid paralysis (NPAFP)," which describes essentially the same symptoms. When one considers the scale of Indian eradication campaign, 47,500 cases of NPAFP, while immense, are within the realm of feasibility. According to the article:

The government of India used 2.3 million vaccinators, who visited over 200 million households to ensure that the nearly 170 million children (under five years in age) were repeatedly immunised with oral polio vaccine.

If the 47,500 case figure for NPAFP is correct, the actual scale of vaccine-related adverse effects associated with oral polio vaccine are probably 2-3 orders of magnitude higher than officially reported by the governmental and non-governmental agencies promoting their use, and by those agencies who are responsible for monitoring and reporting their adverse effects.

Cases like this illustrate how important it is that we all take a critical look at the first-hand vaccine statistics and research itself, reading between the lines when the lines have been intentionally manipulated and the truth obfuscated. For several years, our ongoing project has dedicated itself to providing the research community an alternative medical and toxicological resource for ascertaining the true risks and/or unintended consequences of conventional medical interventions such as vaccinations.

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Dentists Warn That Brushing Too Soon After Eating May Actually Do Damage

by Rob Waugh

Many people brush more than the recommended number of times per day – especially after a rich meal.

Detox Protocol

But dentists warn that the extra brushing could be doing more harm than good.

Brushing within half an hour of eating a meal or drinking a cup of coffee could ensure your teeth suffer worse damage.

After drinking fizzy or acidic drinks, the acid burns into the enamel of your teeth – and the layer below the enamel, called 'dentin'.

Brushing at the 'wrong' time – particularly within 20 minutes of finishing a meal – can drive the acid deeper into your teeth, corroding them far faster than they would have rotted by themselves.

'With brushing, you could actually push the acid deeper into the enamel and the dentin,' says Dr Howard R. Gamble, president of the Academy of General Dentistry in an interview with the New York Times.

Research has shown that teeth corrode faster if they are brushed in the half hour after an acidic soft drink, which 'stripped' them – demineralising them.

Volunteers wore human dentin samples in their mouths, and tested different brushing regimens.

Brushing in the 20 minutes after a soft drink damaged teeth noticeably – although anyone who's just eaten a spicy meal might be relieved to know that waiting an hour seems to be enough to avoid the negative effects.

'However, after intra-oral periods of 30 and 60 min, wear was not significantly higher than in unbrushed controls,' say the researchers.

'It is concluded that for protection of dentin surfaces at least 30 min should elapse before toothbrushing after an erosive attack.'

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If Depression Isn’t A Chemical Imbalance, Then What Is It?

by: Larry Malerba, DO

(NaturalNews) Contemporary scientific culture has fed us the mantra that depression is the result of a chemical imbalance for so long now that the premise is rarely questioned by the general public. On the other hand, there are many in the alternative health community who have been aware of this for a long time (1).

SAMe

Lithium Orotate

Such an overly simplistic explanation suits the needs of a medical establishment that can only think of illness in biochemical terms. It conveniently dispenses with the inherent messiness of human suffering and its almost infinite variations. The general lackluster outcomes resulting from the chemical solution (antidepressants) for this so-called chemical problem should be the first indication that something is seriously amiss, and that maybe medicine doesn't really know what it's talking about.

To discredit the chemical imbalance theory would be to poke holes in the neat little illusion that depression is one monolithic condition, differing only in its duration and severity. It would also disrupt medicine's need to simplify and categorize illness in predictable ways that give the impression of scientific understanding and control. The last thing medicine will tolerate is the loss of its authority as the one and only source of expert opinion when it comes to health and illness. That medicine offers only biochemical solutions is a testament to its stubborn refusal to learn anything new. And so it continues to bark up the wrong tree, looking for biochemical-physiological explanations and answers where they are not to be found.

So if the vast majority of depressions are not the result of chemical imbalances, then what are the causes? The answer is that the causes are as varied as the individuals that experience depression. Although cookie-cutter medicine is ideologically predisposed to disbelieve this answer, it is, nevertheless, the conclusion drawn by most astute holistic practitioners.

First off, we must address the normal variant of depression that most individuals will experience at some time in their lives. Like sadness, joy, excitement, anger, fear, jealousy, and worry, depression is a normal human emotion that plays an important role in mental health and well-being. Just as with any emotion, to hide it or to deny it is to risk encouraging it to snowball into a larger and more formidable issue.

All emotions, including depression, require that we first acknowledge their presence and influence upon our psyches before they can be successfully resolved. This is the primary value in any effective form of talk therapy. Verbalize it, process it, assimilate the implications, release it, and move on. Depression of this type serves a very important function. It provides the impetus that allows us to reflect upon the decisions we have made and the actions that we have taken, which play a large role in the direction our life has taken. Depression allows for critical course corrections that can make a world of a difference in the long run.

Depression is commonly the result of letting other unprocessed emotions and life issues build up over time. Men are particularly prone to depression that comes from their macho, stiff upper lip conditioning, which discourages them from expressing how they really feel. They have thoroughly assimilated the twisted cultural message that to express anything but a false sense of strength and control is akin to being weak, impotent, and inadequate. Little do many men – and women – know, that it is a true sign of strength and courage to be able to face one's emotions and issues squarely without hesitation. Most of the time this is all that is required because, once that first step is taken, resolution is usually not far off.

Of course, there are also many forms of depression that one can't just talk one's way out of. One such very common variant is the depression that comes with having to endure the consequences of chronic illness. Chronic pain and other medical conditions can limit the lives of individuals in ways that interfere with their goals, intentions, and personal freedom. As a consequence, they may find themselves struggling with depression over the loss of their previous state of health and well-being.

The logical solution in such cases is to address chronic illness in an effective way that leads to greater health and vitality. Once this is accomplished, depression becomes no longer necessary. Unfortunately, conventional medicine has a generally poor track record in handling most chronic illnesses. It's prescriptions and interventions are usually only palliative and often complicate matters in such a way as to exacerbate depression. Antidepressant therapy makes little sense in cases of depression that are secondary manifestations resulting from chronic illness. Chronic illness, therefore, is best addressed with a variety of holistic measures including lifestyle changes such as yoga and meditation, diet and nutrition, and non-toxic therapies like acupuncture, homeopathy, Chinese medicine, and Ayurveda.

Grief is a state that can contribute to and mimic depression, and it is poorly served by antidepressant therapy. Grief in its early stages is a normal response to loss. It should be respected for what it is and given ample time to work itself out. Even though some of its symptoms are similar to symptoms of depression, grief is usually not a medical condition. The exception, of course, is when a person's well-being is threatened, as in the case of suicidal feelings resulting from loss.

Surprisingly, the American Psychiatric Association is considering making changes to its bible, the Diagnostic and Statistical Manual (DSM), which would encourage physicians to diagnose depression in cases of normal bereavement if patients experience depressive symptoms for more than two weeks (2). This is a prime example of the ever-encroaching trend toward medicalization that threatens to engulf American life and culture.

It is true that grief can linger for long periods and that some can become stuck in its grip. When grief becomes chronic it can look just like depression, the difference being its etiology stemming from loss. I have found that just a few homeopathic medicines – including Ignatia, Natrum muriaticum, and Aurum – are capable of handling most cases of chronic grief quite successfully (3). It is best to consult a trained practitioner in such cases.

Another variety of depression is the type that accompanies female hormonal changes. Unfortunately, this is a very common problem that is not caused by faulty brain chemistry as much as it is a function of hormonal imbalance. Such imbalances can be triggered by normal hormonal events such as the first onset of menses, pregnancy, miscarriage, labor and delivery, and menopause. Another factor that can alter normal hormonal function is the ever-increasing presence of hormonally active substances that have found their way into the food chain through big agriculture and pharmaceutical waste products.

Not surprisingly, the most common causes of hormonal imbalances that result in depression are routine medical interventions. Top on the list here are birth control pills, whether they are prescribed to prevent pregnancy or to treat already existing hormonal symptoms such as irregular periods, pain and cramping, hot flashes, and so on. Similarly, hysterectomies, tubal ligation, abortions, intra-uterine devices (IUD's), and fertility treatments can alter the balance of normal hormonal functioning. The bottom line is that hormonal balance is a delicate matter than can be easily thrown out of kilter. And hormones are very powerful substances that can affect the entire physiology of a person.

In my experience, medical tinkering with hormonal balance by introducing estrogens, progesterone, and testosterone is fraught with difficulties and usually leads to further hormonal dysfunction. Even bio-identical hormones are capable of disrupting hormonal balance. Again, I have found that good homeopathic prescribing can often restore hormonal balance, thus resolving any hormonally related depression.

Many forms of depression are situationally induced. Bad relationships, abusive home environments, and unfulfilling jobs are just some of the situations that can precipitate depression. In such instances, antidepressants are merely palliative at best and can often contribute to enabling the dysfunctional circumstances to continue. Social services, individual and family counseling, proper nutrition and exercise, and yoga and meditation, are just a few options that will better serve individuals struggling under such difficult conditions. As these individuals become empowered, they can then make the changes necessary to extricate themselves from their painful situations, thus diminishing the likelihood of depression.

There are whole host of additional conditions that may be classified as depression but are more accurately considered categories of their own. Poor self-esteem is a very real problem that may resemble depression. Some cases of depression may be constitutional in the sense that it can be very difficult for a mild mannered person by temperament to express anger or to stand up for him or herself – and this can lead to depression. Teenagers who have undergone growth spurts often experience strong fatigue, which may be mistakenly labeled as depression. Likewise, it is not unusual for a person who has never fully recovered from a bout of mononucleosis to be lumped into the depression category.

Many individuals suffer from fatigue, apathy, indifference, or lack of energy for a variety of complex reasons. By default they tend to be labeled as depressed and given antidepressants because the medical system lacks imagination when it comes to understanding these problems. Medical science has little tolerance for the uniqueness and diversity of human suffering and is forever searching for ways to fit the round pegs of human illness into its square diagnostic holes.

The one type of depression that may actually represent a form of chemical imbalance is the kind that comes from organic brain dysfunction such as that which results from a concussion or head trauma. Even then, homeopathic medicine has documented the relationship between head trauma and depression for over 200 years – and the good news is that it has a number of therapeutic options that can relieve such depressions (4).

While antidepressants may be indicated in a small percentage of cases, it should be understood that they are almost always temporary measures that will not satisfactorily resolve the actual problem. Standard drug therapy tends to be a short-sighted cookie cutter solution for a broad spectrum of unique problems that necessitates more personalized treatment if genuine success is to be achieved. A true revolution in the way we think about health and illness will be a prerequisite to such personalized treatment, which is currently available only from holistic, integrative, green healers and practitioners.

References:
1. Giannakali. Chemical imbalance myth takes a big public fall, Jan 25, 2012, BeyondMeds.com
2. Richard A. Friedman, M.D. Perspective: Grief, Depression, and the DSM-5,
New England Journal of Medicine 2012; 366:1855-1857, May 17, 2012
3. Larry Malerba, DO, DHt. Could Grief be Causing Your Chronic Illness?, Sept 2, 2011www.DocMalerba.com
4. Larry Malerba, DO, DHt. Unexpected Help for Victims of Traumatic Brain Injury, Aug 31, 2011, www.DocMalerba.com

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Giant Nuclear Cover-up?

by: Ethan A. Huff

(NaturalNews) June 6, 2012, was a very strange day for northern Indiana and southern Michigan, where a series of strange explosions and a subsequent nuclear radiation spike left local residents combing for answers. And though there are still many missing pieces to the puzzle, it has become clear that some type of nuclear cover-up is taking place in the region, which is further evidenced by numerous eyewitness accounts of intense shaking and loud booms, audio recordings of inexplicable explosions, and pictures of unmarked aircraft flying during and after the incident.

Radiation Protocol

It all began when separate radiation monitoring stations — a privately-owned Radiation Network station near South Bend, Ind., and a U.S. Environmental Protection Agency (EPA) RadNet station near Fort Wayne, Ind. — detected extremely high levels of nuclear radiation around the same time between June 6 and June 7. Both stations reportedly began to give radiation readings ranging as high as 7,139 counts per minute (CPM), when a normal reading is typically between five and 60 CPM.

You can view a screenshot of the Radiation Network reading, which was later pulled, here: http://www.naturalnews.com/images/Map-US-Radiation-Meters.jpg

As you can see, the South Bend reading shows a shockingly high 7,034 CPM radiation level, which the group later said was incorrect and the result of an "equipment malfunction" (http://www.radiationnetwork.com/Message.htm). But the EPA's RadNet station, which is located about 90 miles away from Radiation Network's South Bend station, also showed elevated radiation levels around the exact same time and on the same day, which leads to more questions about what is really going on here.

RadNet's data has also since been pulled, which is highly suspicious. But if you visit the RadNet Query page (https://cdxnode64.epa.gov/radnet-public/query.do), you can pull up the data yourself from the archive. Simply input "Beta Gross Count Rate (CPM)" in the Selected Parameters box, select Fort Wayne as the Fixed Monitor Location, and select June 6 as the Time Range Criteria.

What you will see are radiation readings that peak as high as 182 CPM around noon on June 6, and suddenly drop to 18 CPM a little more than an hour later. According to the EPA, any CPM level above 100 is high enough to trigger an alert, and yet no official alert was ever issued. In fact, neither the EPA nor anyone else in the government or mainstream media even mentioned the incident, which is now being disregarded as coincidental equipment errors.

Similar high readings were also output by Black Cat Systems, another radiation level tracking site (http://www.youtube.com/watch?v=AwsVLmfZsxk). According to Radiation Network, some of its own stations feed information to Black Cat, which could explain similar incorrect radiation readings being displayed. However, Radiation Network has not confirmed whether or not its South Bend station is one of the readings shared by Black Cat.

Eyewitness accounts indicate strange activity taking place during nuclear anomaly
But the real question here, regardless of the potential Black Cat link, is how could two separate radiation stations nearly 100 miles apart both have equipment errors on the same day around the same time? And what about all the other strange activity that reportedly took place the day of the "faulty" readings, including the deployment of U.S. Department of Homeland Security (DHS) "hazmat" fleets that had allegedly not been moved in years, but that suddenly disappeared?

According to a Reddit reader whose eyewitness account was confirmed by various other readers, a large fleet of DHS emergency response trucks disappeared on June 6 from a parking lot where they had remained unmoved for years. The missing trucks were allegedly emblazoned with a U.S. Federal Emergency Management Agency's (FEMA) National Incident Management System (NIMS) logo, which suggests that a major emergency had occurred that required immediate attention (http://www.infowars.com).

A series of loud explosions that began more than a week prior to the high radiation readings were also reported throughout the region, which adds another element of mystery to this whole situation. WWMT Newschannel 3 ran a report in late May about the occurrence of a "loud explosion like thunder" that resulted in intense shaking felt throughout several Michigan counties. The rumbling was so loud and intense that one local man thought something had exploded inside his house (http://www.youtube.com/watch?v=3oKj_ptBOUE).

In the days that followed, other area residents also reported hearing strange "boom" sounds, and some even reported seeing unmarked helicopters, A-10 Thunderbolts, which are sometimes referred to as the "world's deadliest aircraft," and various other military aircraft and personnel moving in and out of the area (http://naturalsociety.com).

One man who tried to investigate the source of another unidentified explosion further north in Michigan was actually arrested after trying to question the Executive Secretary at the Alpena Combat Readiness Training Center, a year-round National Guard training and exercise facility (http://www.youtube.com/watch?v=AAphZIusdTo).

Some have suggested that either earthquakes or mining operations are potentially to blame for all the strange events. But according to the U.S. Geological Survey (USGS) data, there have been no registered earthquakes detected in the southern Michigan or northern Indiana areas during the time frame in which the numerous large blasts, the intense ground shaking, and the nuclear incident occurred. And many area residents say the explosions and shaking they experienced are unlike anything they have ever experienced before.

So the situation in Michigan continues to remain a mystery that nobody in the mainstream media or government is willing to address, let alone try to solve. Should any further details emerge, NaturalNews will present them for our readers to consider and investigate.

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North Dakota Has It Right, Let’s End All Property Tax

BISMARCK, N.D. — Since Californians shrank their property taxes more than three decades ago by passing Proposition 13, people around the nation have echoed their dismay over such levies, putting forth plans to even them, simplify them, cap them, slash them. In an election here on Tuesday, residents of North Dakota will consider a measure that reaches far beyond any of that — one that abolishes the property tax entirely.

“I would like to be able to know that my home, no matter what happens to my income or my life, is not going to be taken away from me because I can’t pay a tax,” said Susan Beehler, one in a group of North Dakotans who have pressed for an amendment to the state’s Constitution to end the property tax. They argue that the tax is unpredictable, inconsistent, counter to the concept of property ownership and needless in a state that, thanks in part to wildly successful oil drilling, finds itself in the rare circumstance of carrying budget reserves.

“When,” Ms. Beehler asked, “did we come to believe that government should get rich and we should get poor?”

An unusual coalition of forces, including the North Dakota Chamber of Commerce and the state’s largest public employees’ unions, vehemently oppose the idea, arguing that such a ban would upend this quiet capital. Some big unanswered questions, the opponents say, include precisely how lawmakers would make up some $812 million in annual property tax revenue; what effect the change would have on hundreds of other state laws and regulations that allude to the more than century-old property tax; and what decisions would be left for North Dakota’s cities, counties and other governing boards if, say, they wanted to build a new school, hire more police, open a new park.

“This is a plan without a plan,” said Andy Peterson, president and chairman of the North Dakota Chamber of Commerce, who acknowledged that property taxes have climbed in some parts of the state and that North Dakota’s political leaders need to tackle the issue. “But this solution is a little like giving a barber a razor-sharp butcher knife — and by the way, this barber is blind — and asking him or her to give you a haircut. You’ll get the job done, but you might be missing an ear or an eye.”

Polls conducted last month and last week suggest that voters here overwhelmingly oppose the ballot measure to ban the property tax.

Still, even if the measure here fails on Tuesday, the notion is picking up steam in some Republican circles in other states, including North Carolina, Texas and Pennsylvania.

“No tax should have the power to leave you homeless,” said Jim Cox, a state representative in Pennsylvania who has proposed legislation to eliminate the school property tax in the state where, he said, such taxes have led to residents’ losing homes to sheriff’s sales, entering into reverse mortgages or simply moving away.

In a way, North Dakota, though 48th in population among the states, was a logical place for such a movement to brew. While the state’s property tax collections per capita generally fall near the middle among states, the surge in oil production over the past five years, mainly in the western portion of the state, has seen its effects ripple through other parts of life here. The state’s coffers are full, overflowing even. Assessments of home values, especially in some areas, have risen drastically too.

The political mood here, too, leans toward Republicans (who dominate Bismarck), small government, little intrusion and fiscal conservatism. Though opponents to the property tax here received a $12,000 donation in 2010 from the American Tax Reduction Movement, a sister group to the Howard Jarvis Taxpayers Association, which grew out of California’s Proposition 13, members say the efforts here were largely organic, the result of unhappy property taxpayers getting fed up.

“The same problem kept coming up,” said Charlene Nelson, a homemaker who became a leader of the effort to amend the Constitution, pointing to what she deems the underlying problem with the property tax. “It means all of us are renters — none of us are homeowners.”

In recent years, state officials sent more money to localities to pay for schools in an effort to lower property tax bills. But opponents of the property tax said those efforts did not go nearly far enough, and collected nearly 30,000 signatures on petitions to bring the matter to the ballot.

Those who want to keep the property tax have vastly outraised the opponents, gathering more than $500,000, campaign finance reports show. Though the question is among four on ballots here on Tuesday — including the highly contentious question of whether the University of North Dakota should give up its Fighting Sioux nickname — residents here said they had been deluged with information about the property tax measure, on signs, in radio talk shows and through months of debates in school gymnasiums and recreation halls in small towns like Edgeley and Bowman.

For his part, Gov. Jack Dalrymple, a Republican, said he opposed the property tax ban. “It’s mind-boggling, really,” he said, in an interview, of the effects of such a ban. “We’d be changing everything, frankly.”

The notion, he said, that the state has enough surplus to replace property taxes for localities around the state without raising other taxes is false. For starters, he said, much of the state’s benefits from the oil boom are already dedicated legally to particular funds and cannot simply be transferred to support schools, counties, towns, park districts and the like.

Even if the ban fails, North Dakota lawmakers now seem all but certain to tackle broader solutions to the property tax question as early as next year.

“I have to say that we totally understand that North Dakotans are very concerned about their property tax payments,” Mr. Dalrymple said. “You have a tension there, and people say this can’t keep on.”

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Omega-3 and Vascular Disease

by Pat Robinson

Omega 3 fatty acids improve the cardiovascular risk profile of subjects with metabolic syndrome, including markers of inflammation and auto-immunity.

  • Omega-3 in modest doses reduces cardiac deaths, and in high doses reduces nonfatal cardiovascular events.
  • Dietary supplementation with omega-3 fatty acids reduces the incidence of sudden cardiac death in patients with myocardial infarction.
  • Omega-3 fatty acid reduce the total mortality and sudden death in patients with left ventricular systolic dysfunction.
  • Raising blood levels of omega-3 fatty acid levels may be 8 times effective than distributing automated external defibrillators (AEDs), and 2 times more effective than implanting implanting cardioverter defibrillators (ICDs) in preventing sudden death
  • Omega-3 fatty acid supplementation reduces total mortality and sudden death in patients who have already had a heart attack.
  • Consuming small quantities of fish is associated with a reduction in coronary heart disease.
  • Omega-3 fatty acids and vitamin D supplementation results in a substantial reduction in coronary calcium scores and slowed plaque growth.
  • Omega-3 fatty acids improve macro- and microvascular function in subjects with type 2 diabetes mellitus.
  • Fish oil improves tubular dysfunction, lipid profiles and oxidative stress in patients with IgA nephropathy.
  • In patients with stable coronary artery disease, an independent and inverse association exists between n-3 fatty acid levels and inflammatory biomarkers.
  • Omega-3 fatty acids improve endothelial function in peripheral arterial disease.
  • Fish oil has a beneficial effect on blood viscosity in peripheral vascular disease.
  • Fish oil supplementation improves walking distance in peripheral arterial disease.
  • The omega-3 fatty acid docosapentaenoic acid (DPA)reduces the risk of peripheral arterial disease associated with smoking.
  • Fish and long-chain omega-3 fatty acid intake reduce the risk of coronary heart disease and total mortality in diabetic women.
  • Higher plasma concentrations of EPA and DPA are associated with a lower risk of nonfatal myocardial infarction among women.
  • Omega-3 fatty acid consumption is inversely associated with incidence of hypertension.
  • Fish oil, but not flaxseed oil, decreases inflammation and prevents pressure overload-induced cardiac dysfunction.
  • The consumption of fish reduces the risk of ischemic stroke in elderly individuals.
  • Fish consumption reduces the risk of ischemic stroke in men.
  • Eicosapentaenoic acid (EPA) may have a therapeutic role in attenuating pulmonary hypertension.
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The Corporate Buy-out of The Health Food Industry

by Dr. Richard Schulze

 

The growing trend over the last few decades seems to be the almost endless selling by owners of their small companies to huge international corporations. I wouldn't mind this trend, if I thought it was in the customers’ best interest, and furthermore, if what I experienced was that the products got better. Instead, what I almost always see is that the products get worse. This trend is usually NOT in the consumers’ best interest at all.

Usually, when small companies sell out, the founder’s passion, vision and purity gets lost, as the new parent company focuses on cost, bottom lines, larger distribution and even larger profits. This results in their quest to make the products cheaper, and results in inferior products that don’t work as well, don't last as long, and are more disposable.

Recycled has even become Recyclable, the new product buzzword, which doesn’t mean anything. Actually, it means that the company didn't do a damn thing in sourcing out their raw materials, didn't use anything recycled, and they're just asking you to take on what is their responsibility and dispose of the product in a conscious way, if this is even possible.

I still have my father's tools, and some of these tools were his father's tools. Steel, iron and wood, and with a little oil, the oldest tools still work like the day they were made. You can’t buy tools like this anymore. Half the screwdrivers I buy nowadays, strip just using them to screw in a screw, if the plastic handle doesn’t break first. They just don't make things like they used to. OK, I could bitch about this forever, and I’m starting to scare myself because I’m sounding like my father, so I’ll get to my point…

The Corporate Buyout of our Health
No, I’m not talking about HMO’s, but that’s another thing that didn’t improve medical care, but it did improve insurance companies’ profits. I am talking about the selling of health businesses and herbal medicine companies to big corporations.

Coca Cola bought out Odwalla juice. That was a nightmare. Their bad processes made people sick and caused pasteurization laws to be passed so now we can only buy cooked apple juice.

Pepsi Cola bought out Naked Juice, so now most of our fresh juices are being produced by Coke, Pepsi and other soda pop companies.

Kraft Foods, the people who make Velveeta imitation cheese, bought out Boca Burger, the veggie burger company, and that quality went down. (By the way, Kraft Foods is owned by tobacco giant Phillip Morris.)

Lipton, the huge black tea company, bought out Celestial Seasonings Herbal Teas, and we got prettier packaging, not better product!

Mars Incorporated, the huge candy bar company (M&M’s and Snickers), bought out what used to be an awesome Organic seed and food company, Seeds of Change.

Traditional Medicinal Teas – SOLD and is no longer owned by the great California herbalist Rosemary Gladstar anymore. In fact, I just searched for her name on their corporate website and nothing came back!

Janet Zand’s herbal products – SOLD and is no longer owned by Janet anymore. (By the way, I couldn’t find her name on the company website anymore, either.)

Burt’s Bees – SOLD to Clorox.

Get my point here? The Soda Pop, Candy Bar and Junk Food industries are taking over our Health Food Industry!

Am I Paranoid?
During the days of my clinic, I used to feel like the government was closing in on me—actually it did! Today, corporate giants have surrounded and are circling the health wagon train, and are picking off my friends, students and the health food industry in general, one by one.

(OK, in fairness let’s not blame corporate giants, they make health-destroying junk, but this is not their fault. It is actually the pure greed of my friends, students and the health food industry people, that are selling their companies, and their souls, for the almighty dollar! They are selling the natural foods and natural medicines we made to combat the damage caused by the health-destroying products of these big corporations, TO THE SAME CORPORATIONS!!!)

I would love to believe that this trend is the beginning of a new era, and awakening of American corporations, that Americans want health, and are willing to take more responsibility. My fear is that in this process, of all my students and other herbalists selling their businesses to drug companies and horrible corrupt earth and animal destroying companies, well, these once good products will become trendy names with good packaging, wider distribution, but the quality will degenerate to total garbage! Actually, it is more than a fear, it is happening!

Another One Bites the Dust!
In my life I have had the privilege to teach many great men and women who have gone on to become great herbal doctors and run great clinics. Other people I have trained have gone into the health food and herbal medicine industry. Many years ago, I was fortunate enough to teach two east coast friends, Paul Schulick and Rick Scalzo. Paul Schulick went on to create New Chapter, a natural vitamin supplement company, and Rick Scalzo founded Gaia Herbs, a very good herbal company.

In The News This Week:

Paul Schulick has just sold his natural vitamin supplement company to Proctor & Gamble!

Proctor & Gamble:

– The makers of Crisco, the original crystallized cottonseed oil supplying Americans with a daily dose of health-destroying trans-fatty acids for 100 years now.

– The makers of Pepto Bismol, basically liquid aspirin.

– The makers of Tide, its heavy duty earth polluting synthetic detergent.

– The makers of Crest, and the original fluoride toothpaste.

And let’s not forget Pringles and Prilosec! Yes, Proctor & Gamble makes “over the counter” pharmaceuticals too!

There have been many websites that have made great comments on this sell out by New Chapter to Proctor & Gamble.

Excerpts from a few other recent Blogs, Regarding the Sell Out…

Spread the word: New Chapter is now owned by Proctor & Gamble.

Proctor & Gamble, the global corporate conglomerate that sells a vast array of consumer products containing cancer-causing chemicals and petroleum derivatives, is now the proud owner of New Chapter, one of the more promising nutritional supplement companies we've seen in a while.

New Chapter co-founder Paul Schulick announced, "For us, this has been a dream come true. This is what we have been wanting to do since we started doing this 30 years ago. The world and the United States need this."

Really? The world needs global corporate giants to buy up all the natural product brands? This is one of the many companies we helped publicize and promote, only to see them sell out to corporate giants who routinely take over these companies, cheapen their product formulations, and exploit name recognition to intentionally mislead consumers into buying watered-down, reformulated products.

So now the same company that brings you Tide laundry detergent, Pringles potato chips, Dawn dishwashing soap, and Bounce dryer sheets (can you even think of a more offensive chemical laundry product?) will be bringing you New Chapter supplements, too.

I'm disappointed in New Chapter and Paul Schulick. Here's yet another case of someone who has sold out to the global power elite, apparently oblivious to where this will likely lead.

Paul Schulick has made a deal with that devil, it seems.

Of course, I'm sure Paul has justified it all to himself. The huge financial backing of P&G will allow New Chapter to "expand into more retail outlets," he's probably told himself. The deal will show P&G that natural products can be profitable! It will make nutrition mainstream! Yeah, right.

These stories always have the same ending: The products get watered down, consumers shift their demand to a smaller, trusted company, and the financials of the once-great small company collapse. The big corporation ends up either shuttering it or whoring it out using the same brand name but replacing all the quality ingredients with crap filler and toxic chemicals. The only "winner" in these deals is usually the CEO who sold it, and possibly a few board members who also walk away with millions of dollars while their customers who made them great get left with nothing.

— Natural News.com

New Chapter, a vitamin and supplement company offering worthy products since 1982, has recently been bought out by mega-corporation Proctor & Gamble. Being the owner of chemical laden, toxic products such as Cascade dish-washing soap, Tide laundry detergent, Pringles potato chips, and Bounce dryer sheets, it is evident that Proctor & Gamble is less than a trustworthy and caring company.

Although Schulick’s stated goal of offering the world quality health supplements free of health-damaging substances is commendable, is seeking and accepting the involvement of a corrupt corporate giant really acceptable? The quality of New Chapter’s products will undoubtedly be compromised by such a corporate fuse, with P&G’s poor record of health-devastating products enough to raise the alarm. Truthfully, the teaming up of nutritional supplement companies and corporations like P&G is the last thing the world and United States needs.

— Natural Society.com

New Chapter's co-founder has this to say regarding their sell out,  "For us, this has been a dream come true. This is what we have been wanting to do since we started doing this 30 years ago. The world and the United States need this."

What exactly is Paul Schulick saying that we need? We fear that Proctor & Gamble may change the formulations and make them not so natural and organic anymore much like what happened recently with Kashi.

What is unnerving here is that New Chapter has handed off the reins to a global corporation steeped in chemical products and mass consumerism. Will P&G "adulterate" the products with harsh chemicals and preservatives?

We also noticed an excessive "push" from New Chapter before the end of the last calendar year to purchase more than normal in a "stock-up" fashion and now assume it was to boost their numbers before the end of the tax year.

— My Natural Market.com

Proctor & Gamble on Animal Torture
Proctor & Gamble, the corporate conglomerate which recently bought out organic supplement and vitamin company New Chapter, has a long and extensive history of engaging in cruel animal testing…. and has been lying for years about making efforts to switch to cruelty-free testing alternatives.

P&G continues to torture dogs, rabbits, hamsters, guinea pigs, and other creatures by conducting experiments on them that include poisoning them with toxins, burning their eyes with chemicals, and eventually killing them, and P&G does not even provide basic care for these animals while they are still alive.

P&G ‘scientists’ do not sedate the animals or give them painkillers when they place the animals in restraining devices so they cannot struggle while the workers apply the chemicals, which burn into the animals' eyes and skin, where the animals sometimes break their necks or backs attempting to escape the pain.

P&G’s animal torture includes forcing dogs to eat large amounts of cleaning chemicals by pumping them directly into their stomachs.

— Natural News.com

Finally…

Street rumors say that the company was sold to pay off investors, and that was not what the owner wanted to do, but had no choice.

Officially, Paul Schulick is quoted as saying that he didn’t make this decision for the money. If not, then why would he sell his company? He is also quoted as saying, “this is a dream come true” and has been his goal for 30 years. His dream, our nightmare!

— Dr. Schulze

PS: I don’t play well with others. Therefore, I have no investors or stockholders in Dr. Schulze’s, nor my American Botanical Pharmacy. I have no financial pressure. I make all the decisions. I have one goal: YOU getting well and staying well, naturally. This keeps life the way I like it—simple.

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The Lack of Evidence For Postdate Birth Induction

by Judy Cohain, CNM

Abstract: Case controlled studies show no benefit to inducing for postdates. Routinely inducing for postdates is based on 3 uncontrolled, retrospective studies showing 1/1000 less stillbirths while ignoring possible increases in brain damage to newborns as a result of induction. Induction or Elective cesarean for Precious pregnancies is justifiable.

Membrane Complex
Magnesium Oil

There is a low risk of stillbirth at ≥42 weeks in the US although it is even lower in Europe.  Once you get to term, the chance of a healthy woman delivering a live baby is 99.95% in Europe and 99.90% in the US. If post-term induction were to be shown in the future to have the capability of preventing stillbirth without increasing brain damage and perinatal mortality, about 2,000 healthy, low risk women would have to be induced at 40 weeks to prevent one stillbirth.

Stillbirth and Neonatal death happen throughout pregnancy (1,2).

Term stillbirth and perinatal mortality rates: European rates in red , US rates in blue

Week Stillbirth/1000 undelivered Neonatal deaths/1000 live births
37 1/3000         1/1400 2.7/1000
38 1/2500         1/1250 1.5/1000
39 1/1800         1/1000 0.9/1000
40 1/1300          1/800 0.7/1000
41 1/800            1/750 0.9/1000
42 1/600            1/900 1.3/1000

It is expected that 98% of women do NOT deliver on their due date, but rather 49% before and 49% after their due date, and only 2% on their due date. Since first births on average deliver a week after the due date, about 75% of first births deliver after their due date.  Data from 2002-2008 in the US showed  11.4% of low risk first births and 6.4% of low risk multiparous births that attempted vaginal birth were induced for the reason of  'postdates’ and a total of 45% of births, that were not elective cesareans, were induced.

Inducing for postdates originated from an uncontrolled, non-randomized observational study from 1999 showing a drop of 1/1000 in the stillbirth rate at several hospitals, occurring serendipitously during the same time frame as an increase in the induction and cesarean rates in Canada.  The drop in stillbirths in this type of research can be explained by a change in many other possible variables that took place during the same time period. This result has never been shown by case controlled trials. The best quality evidence says that induction for postdates does NOT reduce the number of stillbirths or improve perinatal mortality rates.

The best quality evidence says that induction for postdates does NOT reduce the number of stillbirths or improve perinatal mortality rates.

Documented Drawbacks of routine induction: High induction rates are associated with an increase in premature births between 34–36 weeks, increased births of problematic babies that need intensive care,  higher cesarean rates and 1 in 3000 maternal deaths due to cesarean, a possible increase in brachial palsy due to undo force of induced contractions, and two fold increase in amniotic fluid embolism.

There is some logic behind a desire to deliver In Vitro Fertilization (IVF) pregnancies at 40 weeks to avoid the rare cases of stillbirth that take place after 40 weeks. Since you know when fertilization took place, you know when the fetus is fully developed.  IVF babies are particularly precious since they may not be replaceable. There is some logic behind delivering uncontrolled diabetics early to avoid stillbirth for similar reasons. 

The same cannot be said for non-IVF pregnancies. Ultrasound dating is only accurate to the nearest 2 -4 weeks. A woman who thinks she is 40 weeks by 10 week ultrasound, might only be 36 weeks and if induced, the fetus may need intensive care, and therefore would be more vulnerable to problems such as infection.  About  90% of pregnancies currently defined as post term would not be so if instead of rounding out pregnancy to 40 weeks (280 days) it was counted as 284 days.  When 284 days are used to define pregnancy instead of 280, less than 1% spontaneously deliver ≥2 weeks late, rather than 10%. 

If a prenatal test could predict which pregnancies would end in third trimester stillbirth, then doctors could do the test and induce those pregnancies. But, no prenatal test has been shown to predict stillbirth, therefore doctors are only left with the option of inducing all postdate births or none of them.   

First births on average deliver at 41+0 weeks or 287 days.  In the absence of any other explanation for delayed birth in primiparous women, this phenomenon appears to be explained by the increased level of anxiety of women on their first pregnancies. Women who want to finish a doctoral thesis, attend a wedding, or an important event are well known to deliver after their desired action is finished. Women who go past 42 weeks either have incorrect dating, a wedding they don’t want to miss etc., or fears directly or indirectly related to the birth, family or mothering that have not been dealt with.

Having warm care providers available helps prevent prolonged pregnancy and therefore stillbirth. Having one-on-one midwifery model ongoing support in which fears are expressed and dealt with, the mother starts birth informed and knowing that the person they want will be available and attending the birth, and the same stillbirth rates and perinatal mortality are obtained with much lower cesarean rates, as with medical management with routine induction at 41 or 42 weeks.

What is the research evidence

Postdate induction is based on unreliable ultrasound dating. Pregnancy is about 284 days not 280.

The only pregnancies in which the approximate time of fertilization is known are In Vitro Fertilization (IVF) pregnancies.  The fertilization of IVF pregnancies is known to take place somewhere within 18 hours of combining egg and sperm in the Petri dish. This knowledge of fertilization has been used in studies to see how accurate first trimester ultrasound is in establishing due date.

Ultrasound specialists, blind to conception date of IVF pregnancies, were only able to estimate the age of the IVF pregnancies within -15 days and +14 days of the actual known due date in the first trimester. (4)  Among accurately dated IVF pregnancies, if ≥284 days were used to define pregnancy, instead of ≥280 days, in the absence of induction, post term pregnancies would account for less than 1% of pregnancies (4).  That means that if pregnancy is considered 284 days instead of 280 days, less than 1% of women would go beyond 42 weeks, instead of about 10%.

According to the 1980 edition of Williams Obstetrics Textbook, published before the widespread use of labor induction for postdates, 10% of pregnancies persist for 42 weeks or more. In a large study done with the intent to reduce post term pregnancy using ultrasound, the post term rate was reduced to 2.5%(5). However, in a 2010 study from Sweden using a population of over 1,175,000 singleton births from gestational week ≥37, for which 95% had first trimester ultrasounds, 9% of pregnancies still persisted for 42 weeks or more (6).

In a study of 17,000 Finnish women from 1993–98 trying to prove the usefulness of ultrasound dating between weeks 8 and 16, 10% of women went post term. (7). When two days were added to the length of pregnancy from LMP, only 6% of deliveries were post term(7). This is the only study of first trimester ultrasound that also looked at outcomes, and it found no increase in perinatal mortality among deliveries after 42 weeks. 

Research comparing induction to waiting

Stillbirth and perinatal death occur at every week of pregnancy.  BUT induction of labor at any week has not been shown to decrease stillbirth or overall perinatal mortality and may increase maternal and newborn morbidity. The stillbirth rate after 40 weeks is 1/2000 pregnancies(8). Does inducing 2000 women at 40 weeks prevent one stillbirth?  Systematic reviews say NO. Systematic Reviews of the research which were large enough to study perinatal outcomes have found no significant difference in perinatal mortality including stillbirths between induction and expectant management groups(1,9,10*, , and 11).

The studies supporting induction at 41 weeks are 3 low quality observational studies. The first is co-authored by Mary E. Hannah, author of Breech Trial, who persistently presents "data with serious concerns as far as study design, methods, and conclusions with frequent lack of adherence to the inclusion criteria."(12). Hannah’s 1999 article promoting induction for post term linked two things that may not be related: the stillbirth rates in Canada as a whole and the induction rates reported at Canadian hospitals close to where she lives, between 1980–1995(13). Perinatal mortality rates were not examined during the period. Stillbirth rates went down from 3/1000 to 2/1000.

This could have been the result of greater availability of abortion on demand, improved hospital protocols, prenatal care, nutrition, and/or less smoking or other unknowns. During the 15-year study period, induction rates increased or decreased at different rates in each place, but in general increased from 12% to 16%. Cesarean rates also increased. It is not made clear by how much; only small samples of cesarean rates at 40 and 41 weeks in the years 1986, 1992 and 1995 are given (13). Hannah’s study compares induction in one place to stillbirth rates at different places during the same time period. The studies neglect to report on perinatal mortality, and withhold known cases of babies who were permanently injured directly as a result of postdates induction protocol. (14)

The second study is by a group of five Canadian academics who chose to study American, not Canadian, birth certificate data from 1991–1997 (2). Birth certificate data is known to be unreliable. The birth certificate data used shows no indication of why labor induction was used and the authors admit the data includes inductions for an already dead fetus and for a fetus that was already compromised. Therefore, the outcomes of actual inductions involving a live fetus is unknown. Like the other studies, this study compares stillbirth rates (not perinatal mortality) to approximate induction rates during a six-year period in which induction increased from 10% to 20%.

A third study is again retrospective research using birth certificate data reporting a 1/1000 decrease in stillbirths associated with induction.(15)  Again, the data is birth certificate data. Again important variables that affect stillbirth rates are not controlled for.  This study shows that induction is associated with a significantly higher rate of problematic babies that need intensive care though no long term follow up was made to know if this results in a significantly higher rate of long term brain damage.

All 3 studies admit that it is impossible to draw conclusions or base protocol on their findings since so many factors could lower the stillbirth rate. Nevertheless, those studies are all the evidence there is to support a policy of induction at 41 weeks.

Many doctors are opposed to postdate induction protocols

 "The induction of labour between 41 and 42 weeks is a very crude strategy for reducing term and post-term stillbirth rates. Although the risk of fetal death is increased after 42 weeks, many more fetuses die in utero between 37 and 42 weeks than die in the post-term period. It appears that smaller term fetuses run a far greater risk than their larger counterparts, and that current methods of antepartum assessment of the term fetus are still inadequate" (16).   Difficulty in identifying at-risk fetuses is what has led to routine inductions and better methods are needed(17).

Prenatal testing cannot predict stillbirth or perinatal mortality

As much as we would like a prenatal test and subsequent intervention that would prevent postdate stillbirth, there is none. Risk screening and prenatal tests have many false positive results and the majority of adverse outcomes occur in the larger population of women identified as low-risk. "There is no effective screening test that has clearly shown a reduction in stillbirth rates in the general population"(18,19). Tests that do NOT decrease stillbirth and perinatal mortality compared to control group (19) are:

  • Fetal movement counting
  • Routine ultrasound scanning
  • Doppler velocimetry
  • Detection and management of maternal diabetes mellitus
  • Antenatal fetal heart rate monitoring using cardiotocography
  • Fetal biophysical profile test scoring (BPP)
  • Vibroacoustic stimulation
  • Amniotic fluid volume assessment (AFI)
  • Home vs. hospital-based bed rest and monitoring in high-risk pregnancy
  • In-hospital fetal surveillance unit
  • Use of the partograph during labor
  • Cardiotocography during labor with or without pulse oximetry

Macrosomia

In addition to supposed avoidable stillbirth, another false justification for inducing labor postdates is based on the fact that the healthy fetus continues to gain weight in utero and larger babies may suffer damage on the way out. The 2011 Cochrane Review found three trials involving 372 women rigorous enough to draw conclusions. The evidence shows that induction of labor for suspected fetal macrosomia in non-diabetic women has not been shown to alter the risk of maternal or neonatal morbidity (20).

In countries with relatively low induction rates of 15% (Denmark and Sweden), where 8% of births take place ≥42 weeks, 4% of babies weigh 4500 g or more at birth. In countries like Austria and Belgium, where 40% of pregnancies are induced, only 0.5% of births take place ≥42 weeks, and 1% of babies weigh 4500 g or more at birth(1). Induction results in lower birth weights but not better newborn outcomes. 

Brachial palsy (OBPP) is palsy of the newborn’s upper arm muscles that resolves itself within the first year in about 80% of cases. (shoulderdystociainfo.com) It is caused by damage to nerves in the neck while struggling to deliver a large head in breech birth or stuck shoulders. There is no perfectly accurate way to predict birth weight and even if you could, half the cases of shoulder dystocia (21)  happen when the birth weight is less than 4000 g.

Infants delivered by caesarean section have a lower risk of brachial plexus injury but between 1 and 4% of OBPP cases accompany cesarean surgery.  500 cesarean deliveries would have to be performed to prevent one case of OBPP. More experienced practitioners have a lower incidence of OBPP because the risks may be less if there is no panic, pressure on the fundus, lateral traction or pivoting of the head at the neck or rotational movement of the head in an attempt to rotate the shoulders.

Placental insufficiency

As long as the baby keeps growing, the placenta is obviously functioning well, which indicates that the fetus should be able to tolerate spontaneous labor. Where the baby is thought to have stopped or slowed down its growing, a genetic defect is suspected.

Placental dysfunction is blamed as the cause of miscarriage and stillbirth but there is no evidence to support this theory. Consecutive measurement of the height of the uterine fundus with a tape measure by the same caregiver has been shown effective at picking up the fetus that is not gaining weight. Abdominal measurements facilitate a relationship between a woman and her baby, and educate couples about nutrition, which contributes to better outcomes.

When a fetus is suspected to be small-for-dates, the antenatal care provider can focus on behavioral, social and environmental influences that could be mitigated, including smoking and poor nutrition. Induction has not been shown to improve outcomes perhaps because diagnosis of IUGR is most often wrong and real IUGR babies are probably not good candidates for the difficult labor associated with induction.

Oligohydramnios

Oligohydramnios diagnosed after birth is associated with poorer outcomes, but inducing based on Amniotic Fluid Index (AFI) has never been shown to prevent poor outcomes.  Research comparing AFI in the summer and winter has proven that AFI directly reflects the amount of fluid the mother is drinking and how much she is sweating(22). 

In a 2004 study, scientists failed to find poor outcomes associated with an AFI ≤5 cm measured within seven days of delivery in the third trimester(23). They found no difference in umbilical arterial pH or base excess, even in small-for-gestational-age (SGA) infants, including those with suspected placental insufficiency. There was no difference in the number of SGA neonates, 5-minute Apgar <7, respiratory distress syndrome, necrotizing enterocolitis or neurologic morbidity from matched controls with normal AFI.

"Amniotic fluid stems from the baby’s urine, and the urine results from good blood flow, so if we see low fluid, the assumption is that there is not good blood flow and the fetus is compromised. This study shows the amniotic fluid index is not as good as we thought, and there is no reason to deliver the baby early if other tests are normal"(25).

In a prospective study of 3050 pregnancies, AFI failed to predict lack of fetal well-being and had "no prognostic significance"(24). Cochrane review found "the use of the amniotic fluid index increases the rate of diagnosis of oligohydramnios and the rate of induction of labor without improvement in peripartum outcomes"(25). A 2007 article found that single deepest pocket (SDP) measurement is as useless as AFI (26).

Meconium Aspiration Syndrome

Women are told they need to be induced at 41 weeks to decrease the risk of meconium aspiration. Meconium is not the cause of meconium aspiration. A 2009 review of randomized control trials found pulmonary hypertension and asphyxia, not the presence of meconium, to be the important risk factors for MAS(27). It is likely that perinatal distress and aspiration of meconium occur earlier in the pregnancy, not at birth, which is why suctioning or cesarean delivery does not improve outcomes.

Universal intrapartum suction of infants with meconium stained amniotic fluid has proven useless. Instead, endotracheal intubation and suctioning are currently recommended only for nonvigorous infants. Respiratory failure in infants with MAS is initially treated with mechanical ventilation and surfactant administration.

Suctioning of the hypopharynx is associated with delay in onset of resuscitation, damage to the mouth and hypopharynx, and cardiac arrhythmias secondary to vagal stimulation. A 2009 study concluded, "Routine suctioning is more likely to cause harm than good and should therefore be abandoned as a routine procedure"(27).

A 2009 systematic review (1966–2007) suggests elective induction of labor ≥41 weeks is associated with a decreased risk of meconium stained amniotic fluid, but the lack of quality studies shows a lack of evidence that this translates into better outcomes. Therefore, more research is required before induction can be justified(28).

Drawbacks of Elective Induction for Post term

Elective induction has been shown to increase cesarean rates by 5%(29) Elective cesarean at term has 3X the perinatal mortality of vaginal birth(30). United States statistics show a 13% increase in premature singleton births for the years 1991–2006, the increase occurring among births between 34–36 weeks, with no change in the earlier weeks of prematurity(30). During this period induced labor doubled from 8% to 16%, suggesting "that the increase in the preterm birth rate was related to increases in obstetrical interventions" without any improvement in US infant and fetal mortality rates. 

The rate of amniotic fluid embolism (AFE) is increasing from previous rates of 1/120,000 and occurred in 1/50,000 births from 2005–07 in the United Kingdom(31). Among the 60 cases of AFE reported, half were labor inductions. A 2010 Australian study found the same recent increase in AFE associated with induction (32). Consider this case, of a typical, routine induction: a 40-year-old woman with an unremarkable obstetric or medical history admitted at 41+ weeks for induction due to reduced fetal movement; fetal head down; estimated fetal weight 3600g; cervix not effaced or dilated.

The woman was induced with three prostaglandin E (PGE) doses over 16 hours. Epidural analgesia was administered. At 7 cm membranes were artificially ruptured. Ten minutes later the cervix was fully dilated and the patient started pushing. Respiratory distress appeared and the patient was ventilated and intubated, then died of amniotic fluid embolism (33).