Friday, April 8, 2011

Problems with New Sweetener

UPDATE: August 2010
Here's a toxic sweetener you most likely had never heard of, but I would caution you to make sure you do not ingest it:
HealthEdge's NaturallySweet 
This is manufactured by these folks.

Truvia, Purevia, Zevia, Zerose, Zsweet are marketing names for this artificially blended  erythritol and rebiana mix.  Rebiana is a chemically modified form of  stevia, it is NOT pure stevia.

UPDATE 4, Consumer complaints regarding Truvia

UPDATE 3, 23 December 08: A reader comments on Erythritol as not causing her any problems as noted in our researcher's report. Just like all substances, the ingestion of a substance needs to be in the right form, the right amount, et al, and the effect and outcomes are individual. Please realize that our researcher is a former FDA investigator who has an indepth background in the sciences necessary to make such statements. Please note that the artificial sweeteners referred to, Truvia (Cargill) and PureVia(Whole Earth Sweeteners) are manufactured by these agribusness corporations with an extract of stevia (rebiana)and erythritol and are NOT whole leaf stevia or pure(whole leaf)stevia extract.

UPDATE 2, 22 December 08: Please note that contrary to other reports you may be reading, the FDA DID NOT APPROVE STEVIA. The FDA, in cahoots with Cargill and Coke, approved a synthesized product - as reported originally in this article - manufactured with rebiana (an extract from Stevia) and erythritol (a sugar alcohol).

As Dr. Evangelista states (quoted below): "DO NOT CONFUSE REBIANA (TRUVIA) WITH STEVIA"

UPDATE 1, 20 December 08: Zerose is the Cargill synthesized artificial sweetener made from stevia and erythritol. Zsweet is a similar product in UK and EU. There are numerous scientific studies presenting that this, and related products such as Truvia, may lead to calcium, potassium and phosphate loss with calcification (and lesions) in the kidneys (just like Splenda) and bowel alterations. Please read more.

As to Zevia soda, it seems to me to be quite irresponsible on the part of the company CEO (an attorney)to make the following quote, "Why not supplement a steady breast milk diet with some refreshing ZEVIA?" This quote is associated with a photo of an infant being fed soda by the mother on the company blog. I would suggest the mother is irresponsible as well. While the company web site does not state that Zerose is the sweetener used in their products it does mention that eryrithritol is an ingredient.

I am sure this fellow was not in my 'Social Responsibility of Business' class in grad school.

We suggest Just Like Sugar, unaltered Stevia (order the extract via the Starwest link on this page) and Agave.

We do not endorse the use aspartame or sucralose or any forms of these chemicals, first developed as inseticides, or any products containing them, as they are known toxins to human health, nor do we endorse the use of acesulfame K.
----------------------------------------
12-19-08
The news this morning on NPR seems to be focused on helping you be in the spin on 'rebiana'(Truvia) and how it is "just stevia".

Coke (using Truvia) and Pepsi (using PureVia) are marketing this new artificial sweetener in their beverages but apparently aren't open to presenting both sides of the story.

Even the one TV ad I saw recently for "Truvia" would lead you to believe that this is a safe and natural additive.

Zevia(a soda), because it contains erythritol, may also have similar problems.

The problem is that is may come from natural sources but it is an extracted and modified chemical when it comes out the other end.

DO NOT CONFUSE REBIANA (TRUVIA) WITH STEVIA
Do not confuse this with pure stevia, it is a combination of chemicals with a dab of the stevia plant. Stevia itself is a sweetener and yet they are using Erythritol which is a sugar alcohol known to cause such things as bloating, diarrhea and cramps. That tells you they are not using much stevia. Nor are they removing the poisonous aspartame from Diet Coke and Diet Pepsi. They are simply trying to satisfy a part of the population that knows how deadly aspartame is and wants to use something else.

Notice this sentence: "Stevia was not approved as a food additive by U.S. regulators, but the U.S. Food and Drug Administration issued letters to the companies on Wednesday saying it had no objections to their sweeteners, which are derived from the plant." The FDA has made themselves clear. Industry can do anything they please but they have no intention of approving something safe for the general public. They don't want to displease the aspartame industry who is powerful and takes care of those who defend their poison. Make sure you understand this is a combination of sweeteners and chemicals and not real stevia. The pop companies feel "a dab will do you, so just buy our product regardless of how its made". The public again will be the guinea pigs and lab rats. Also, see the admission that Pepsi's Purevia is being developed with Merisant, an aspartame manufacturer. Nobody should use these products until they are analyzed. Industry is constantly adding small amounts of aspartame because its addictive. If they do this to these products aspartame victims will react because aspartame is so poisonous it causes chemical hypersensitization.
Lab Tests Point to Problems with New Sweetener
Consumer group says product can increase cancer risk
September 2, 2008

A consumer group says a new commercial sweetner, said to be 200 times sweeter than sugar, may cause health problems and needs more study. Coca-Cola and Pepsi are planning to introduce new drinks made with the sweetner, rebiana, an extract of stevia leaves.

In a letter to the Food and Drug Administration, the Center for Science in the Public Interest (CSPI) says the agency should require additional tests, including a key animal study, before accepting rebiana as Generally Regarded as Safe, or GRAS.

The letter cites a new 26-page report by toxicologists at the University of California, Los Angeles, several, though not all, laboratory tests show that the sweetener causes mutations and DNA damage, which raises the prospect that it causes cancer.

"A safe, natural, high-potency sweetener would be a welcome addition to the food supply," said CSPI executive director Michael F. Jacobson. "But the FDA needs to be as sure as possible that rebiana is safe before allowing it into foods that would be consumed by tens of millions of people. It would be tragic if the sweetener turned out to cause cancer or other problems."

One key animal study has not been conducted, according to the UCLA experts and CSPI. The FDA's guidelines advise testing prospective major new food additives on two rodent species, usually rats and mice. The new sweetener has only been tested on rats, but not mice.

The toxicologists' report said that because several studies found mutations and DNA damage, a lifetime mouse study designed to evaluate the risk of carcinogenicity and other health problems was particularly important.

The UCLA toxicologists emphasized the need for more genotoxicity tests, because of the evidence that derivatives of stevia that are closely related to rebiana damage DNA and chromosomes.

Their report noted that much of the recent research on rebiana was sponsored by Cargill and urged the FDA to obtain independently conducted tests to ensure that corporate biases don't influence the design, conduct, or results of the tests.

Rebiana is shorthand for rebaudioside A, a component of stevia. It is obtained from the leaves of a shrub native to Brazil and Paraguay. Coke, Pepsi, and other companies are excited about rebiana, because it supposedly tastes better than crude stevia, which is sold as a dietary supplement in health-food stores.

After all the controversies pertaining to saccharin, aspartame, and other artificial sweeteners, the food industry expects many calorie-conscious consumers to eagerly opt for this natural sweetener.

Two companies -- Cargill and Merisant -- have told the FDA that rebiana should be considered GRAS, a category given less scrutiny by the FDA than ordinary food additives. A third company, Wisdom Natural Brands, has declared that its stevia-based sweetener is GRAS and will market it without giving evidence to, or even notifying, the FDA. That company gave CSPI only a heavily redacted report prepared by scientists it hired to declare its stevia derivative, which is of unknown purity, is safe.

Stevia is legal in foods in Japan and several other countries, but the United States, Canada, and the European Union bar stevia in foods because of older tests that suggested it might interfere with reproduction. New tests sponsored by Cargill did not find such problems.

"I am not saying that rebiana is harmful, but it should not be marketed until new studies establish that it is safe," Jacobson said.

Cargill's version of rebiana is called Truvia and would be used by Coca-Cola. Pepsi's version is called PureVia and is produced by Merisant's Whole Earth Sweetener division. Merisant is best known for marketing the Equal brand of aspartame.

CSPI has not questioned the safety of two artificial sweeteners, sucralose (Splenda) and neotame, but says that suggestive evidence indicates that saccharin, aspartame (Equal, NutraSweet), and acesulfame-K pose small risks of cancer.

"The whole issue of what gets GRAS status needs to be reviewed by Congress," Jacobson said. "It's crazy that companies can just hire a few consultants to bless their new ingredients and rush them to market without any opportunity for the FDA and the public to review all the safety evidence."

Two of the most harmful ingredients in the food supply are considered GRAS: salt, which raises blood pressure and causes thousands of unnecessary heart attacks and strokes every year, and partially hydrogenated oil, which is the source of artery-clogging artificial trans fat. CSPI has long campaigned to get partially hydrogenated oil out of the food supply and to reduce salt to safe levels.
From Consumer Affairs

Fluoride Not a Cavity Preventive

Fluoride in the most basic form, natural or otherwise, is a poison, known for decades not to be effective in reducing cavities.
Fluoridation Does Not Reduce Tooth Decay

Statistics from a study conducted by the New Zealand Ministry of Health suggest that there are no advantages derived from fluoridation. These statistics actually match similar arguments set forth by the American Dental Association.

The latter organization conducted a large study on some 39000 American children and found that they did not derive any advantages from the use of fluoride.

The process of fluoridation is the practice of adding fluoride minerals to a water source so that people can get exposed to the mineral through drinking water. Some bodies of water already have fluoride in them and do not need fluoride added.

The fluoride is allegedly added so that it can help in the prevention of cavity development. The practice of adding fluoride to water is suppose to allow many people, regardless of income, to receive healthy doses of fluoride. Yet, recent studies are revealing that the fluoridation practices do little in terms of cavity prevention, if anything at all.

The study conducted in New Zealand by the Ministry of Health reveals that children living in areas with no fluoride have one percent fewer cavities than those children that reside in regions where fluoridation is offered. Nevertheless, the Health Ministry still asserts that some thirty percent of children will gain some advantages from regular fluoridation.

While the assertion may seem somewhat paradoxical, the statistics offered by the organization mix low and high socioeconomic towns and cities to supply a figure to represent the nation. This mixing of statistics results in a rather poor representation of what is really going on.

Some researchers argue that the statistics would reveal that both groups of tested children would benefit from fluoridation if fluoridation had advantages.

In truth, the statistics are actually revealing that children are simply not benefiting from the use of fluoridation. The bottom line is that the Ministry of Health is trying to make the use of fluoridation sound more promising.

Some researchers suggest that the Ministry is acting against at least fifty years of studies that indicate fluoridation does not provide an adequate defense against cavities.http://worldental.org/dental-news/health-ministry-finds-that-fluoridation-does-not-reduce-tooth-decay/1300/

Thursday, April 7, 2011

Donate and get a free herbal healing $20 CD

Donate today to our organization and receive a free herbal healing CD valued at $20.

This is a Tax Deductible Donation.  All Donations Help Us Continue This Work and Our Service Projects.

Donate soon as we have just a few remaining copies of the CD to give away.

Wednesday, April 6, 2011

HERBDAY - Celebrate on a new day

2010 HERB DAY - SATURDAY 1 MAY
HerbDay Moves to Spring Date = Requests from herb lovers all over the country, HerbDay will officially be celebrated on the first Saturday in May going forward, starting with Saturday, May 1, 2010. More people in more parts of the country have a larger variety of herbs growing at this time of year than do in fall. Since HerbDay is a grass roots movement and belongs to the people, the coalition that got the event started wanted to support the populace in taking ownership of HerbDay by moving it to a date more conducive to a greater number of celebrations across the country. If you already have an event slated for October 2009, please go ahead and have it. Let's keep the momentum going to make the celebration of herbs and their uses an ongoing movement.
In fact, everyone is encouraged to celebrate HerbDay any time they want. If you prefer to continue hosting your HerbDay event in autumn or if summer works better for you, please feel free to do so and continue to list your event in the Organize an Event section of this site. Visitors ask year round for information on events in their area. We will continue to add new useful information as time goes on.

Let's make HerbDay each and every day of the year!
POSTED ORIGINALLY 9/21/08
Celebrate Herbs and Herbalism
HerbDay is a coordinated series of independently produced public educational events celebrating the importance of herbs and herbalism. HerbDay was conceived of by five nonprofit organizations with interests in herbs and herbalism (the HerbDay Coalition), to raise public awareness about the significance of herbs in our lives and the many ways herbs can be used safely and creatively for health, beauty care, and culinary enjoyment. Greater familiarity with herbs will increase informed use of herbal products and build public support for maintaining personal choice in the use of botanicals.

The date for HerbDay 2008 is set: Saturday, October 11

The first HerbDay was held on Saturday, October 14, 2006. The second annual HerbDay was Saturday, October 13. And in 2008, it will officially be on October 11. Some folks celebrate before, during and after that day. Participants in HerbDay 2006 brought together individuals, businesses, and organizations that share a love and passion for herbs and herbal medicine. These include herbalists and health care providers using herbs in their practice; authors, teachers and lecturers with expertise in herbs; herbal product manufacturers and marketers; retailers and distributors of herbal goods; botanical gardens, parks, and schools — and most importantly, the people and families who love to use herbs! HerbDay 2008 will be just as much fun!

The entire herbal community is invited to participate actively in HerbDay 2008, either by hosting an event or providing sponsorship in the form of financial support. Now is the time to start developing ideas for local HerbDay activities to ensure that every community celebrates the wonders of herbs. Visit www.herbday.org to review the initial menu of ideas that the HerbDay Coalition has developed, and to register to tell others what you are planning to do to join the herbal celebration. The website will be the primary location to organize and disseminate information about HerbDay activities and resources.

HerbDay is a coordinated series of public educational events celebrating the importance of herbs and herbalism through harmonized, independently planned activities that will occur on October 11, 2008, and/or during the days leading up to and following that date. Activities will occur at retail stores, botanical gardens, and parks throughout North America. HerbDay activities will be designed by each hosting venue, which will have broad latitude in selecting its own events, such as lectures and workshops by well-known herbalists; herb walks; in-store cooking demonstrations featuring herbs and spices; seasonal herbal handcrafts; in-store herbal beauty product demonstrations; presentations by herb company representatives; activities with herbal themes for children; etc.

Five national nonprofit organizations— American Botanical Council (ABC); American Herbalists Guild (AHG); American Herbal Pharmacopoeia (AHP); American Herbal Products Association (AHPA); and United Plant Savers (UpS) — are working together as the HerbDay Coalition to launch this event.

Bill Gates Needs a Few Lessons

ORIGINALLY POSTED: 1/29/10

Ten Billion dollars will go a very long way to improve health if only it were used to provide super nutrition and supplements that are known to be superior sources of health.

Vaccines just do not prove effective over time and the science proves it.  The Rotavirus vaccine was proven very problematic as has been the pneumonia vaccine.  The AIDS vaccine development was a flop!

Focusing on vaccines really provides welfare to the pharmaceutical industry, little for human beings in need of good food and supplements to help them rebuild their nutritional status.  A few armed guards are needed as well to insure that these life saving items reach the people.

Malaria can be both prevented and treated with supplements and netting.

Drug resistant TB is cured with garlic.  Four vitamins prevent HIV from becoming AIDS.

Bill and Melinda must still be in their wonderland of ignorance, fueled by WHO and Big PhRMA propaganda..
Bill and Melinda Gates announced plans Friday to invest $10 billion in the fight against a number of illnesses including AIDS and said the record donation could save nearly nine million lives.

Speaking at the World Economic Forum in Davos, Switzerland, they said the 10-year program will focus on vaccines for AIDS, tuberculosis, rota virus and pneumonia.

"We must make this the decade of vaccines," said Bill Gates.
http://www.cnn.com/2010/BUSINESS/01/29/davos.bill.gates.donates/index.html
Profitable Depopulation Plot Links JP Morgan-Chase/Goldman Sachs To Vaccination Contamination and BigPharma Corruption
By Dr. Leonard Horowitz, 4-29-10
COURTESY: RENSE.COM

A medical investigation into suspicious outbreaks and propaganda used to sell drugs and vaccines has exposed investment bankers at JP Morgan-Chase (JPMC) and Goldman Sachs (GS) for plotting to shock/stress, frighten, poison, and kill billions of people most profitably--pharmaceutically--according to the Editor-in-Chief of Medical Veritas journal.

While researching a powerful Partnership for New York City (PFNYC), uniting Wall Street's wealthiest industrialists, Harvard-trained public health expert, Dr. Leonard Horowitz, and investigative journalist, Sherri Kane, discovered shocking evidence of a conspiracy to commit global genocide by generating diseases and death to advance profitable pharmaceutical depopulation.

Population planners at the highest levels of government and industry conspired to spread diseases, vaccines, drugs, and death most profitably, according to research published in the latest issue of Medical Veritas.

In a related Special Report posted on YouTube, Dr. Horowitz urged humanitarian organizations and activist groups worldwide to issue investigations, alerts, civil complaints, and criminal charges to stop the pharmaceutical depopulation plot because it risks genetic inheritance, new pandemics, and the possible extinction of the human race.

"Corruption in the drug industry is rampant and transparent," Dr. Horowitz explains. "Investment bankers at JPMC and GS, who acquired controlling interests in the largest drug firms during mergers and acquisitions, have placed 'depopulation' near the top of their list of geopolitical priorities. Their depopulation agents are now in top positions of government, finance, and industry.

The depopulation plan is supported by the world's wealthiest people, including Bill Gates, who admittedly funds vaccinations to reduce global populations by 10-15%. Leading population planners and economic developers advance identical plans to cull the world's population to 1 billion.

"Killing 6-out-of-7 people globally, most profitably, requires planning and an unprecedented conspiracy to commit genocide by applying advances in genetic biotechnologies exclusively available and affordable to drug companies controlled by the investment bankers," Dr. Horowitz adds.

The doctor points to the fact that US Treasury Department officials previously operated JPMC and GS on behalf of majority stock holders and their partners in pharmaceutical companies heavily represented in the PFNYC and the trade organizations that negotiate multi-billion dollar government purchases of drugs and vaccines.

Researchers, including vaccination contamination expert Dr. Viera Scheibner, reports in the current issue of Medical Veritas that polio virus vaccines are produced in African green monkey kidney cell cultures routinely contaminated with transmissible cancer viruses.

By reviewing drug company patents, Dr. Horowitz learned that the makers of H1N1 swine flu and rotavirus vaccines use the same cultures risking recombinations, genetic mutations, and unstoppable transmissions of deadly agents threatening new pandemics.

"This best explains why public health officials are preparing for vaccine-transmitted H1N1s cloned in monkey cells to recombine with bird H5N1s currently circulating. This threatening and most deadly recombination of flu viruses, officials herald may happen in the Fall," Dr. Horowitz warned.

Besides the inadequacies of safety testing new vaccines without using placebo controls, it is this issue of reliability of information that concerns more than half of the medical physicians polled since they became aware that the entire medical industry has been hijacked by Wall Street's pharmaceutical profiteers. Now they are learning from famous people, like Gates, that the world's wealthiest people are administering vaccinations for depopulation.

"I love vaccines," Gates stated at a TED conference in February, 2010, while lecturing on ways to reduce global populations to stem environmental pollution.

The links between the directors of major drug companies, mainstream media moguls, and investment bankers at JPMC and GS are so obvious and incriminating, and the dispersion of unsafe vaccines so common and disturbing, only profitable depopulation as a planned outcome of pharmaceutical investments can explain the current situation.

"Complete censorship was the only option officials have had to prevent a meltdown in public opinion about medicine and the pharmaceutical industry," said Ingri Cassel, a leading vaccine risk awareness activist. "This explains why news of this vaccination depopulation plan has been neglected by the special-interest-influenced media."

Investigating conflicting pharmaceutical interests influencing news coverage, Sherri Kane, previously a writer for FOX News in Los Angeles, learned that the majority shareholders in FOX, TimeWarner, News Corp., and the Wall Street Journal, are heavily invested in GlaxoSmithKlein and Merck's CSL Laboratories, both makers of risky drugs and vaccines.

Lloyd Blankfein, the CEO of Goldman Sachs, became a major shareholder in AstraZeneca following his direction of the company's acquisition of the H1N1 FluMist maker, MedImmune. Blankfein has also leveraged ABC-Disney following their merger with money he raised through GS investors. This resulted in Dr. Oz's heavy promotion of H1N1 vaccines on ABC last year, when officials learned that the vast majority of Americans were unwilling to risk the exposure.

Rupert Murdoch and Lloyd Blankfein co-chair the PFNYC, founded by CHASE principal, World Bank ambassador, and America's leading energy industrialist and medical monopolist, David Rockefeller. The PFNYC was chartered by the Royal Family of England--a majority share holder in General Electric--the world's largest company--that controls NBC/Universal/Comcast, and MSNBC with Bill Gates.

The PFNYC was pledged to play a central role in reconstructing Ground Zero following the 9/11 attacks, according to Kathryn Wylde, President & CEO of the Partnership and current Director of The Federal Reserve Bank of New York. The organization compiled the economic report on the damage done, advanced financial plans for reconstructing the World Trade Center, and advised leading financiers regarding reconstruction investments.

According to 911-Truth movement directors, Wylde and other members of the PFNYC are implicated in the treasonous attacks that scientific evidence says involved thermitic explosives used in controlled demolitions.

These allegations and PFNYC connections to 9/11 events implicating investment bankers at Goldman Sachs are additionally scrutinized in a new feature-length film produced by Dr. Horowitz. PHARMAWHORES: The SHOWTIME Sting of Penn & Teller premieres in theaters across North America this summer. (Quicktime and MP-4 downloadable versions are available through PharmaWhores.com.)

The PFNYC is co-directed by Jeffrey B. Kindler, the Chairman and CEO of Pfizer--the world's largest drug company. Kindler stewards Pfizer through multi-billion dollar acquisitions also involving JPMC and GS financing.

The Pharmaceutical Research and Manufacturers of America (PhRMA), the drug industry's main trade organization, is also directed by Kindler. PhRMA officials engage White House and Pentagon officials in private negotiations determining pricing for stockpiles of drugs and vaccines.

Dr. Horowitz views this covert administration of multi-billion dollar pharmaceutical contracts as symptomatic of the industry's corruption. The "corporate shell game" is played using mergers and acquisitions directed by the same people. Their creation of the PhRMA trade organization provides the illusion of their legitimacy and fair competition. Price fixing occurs behind closed doors, explaining why prices vary so widely internationally.

Another gross example of corrupt government pharmawhores sucking Wall Street's slime, is Congressman Henry Waxman's (D-CA) treason against the American people for sneaking dietary supplement regulation language into 'The Wall Street Reform and Consumer Protection Act of 2009,' (H.R. 4173).

For years, Waxman has attempted to pass legislation restricting consumer access to nutritional supplements on behalf of BigPharma. The FDA, largely controlled by BigPharma, contends regulating vitamins, minerals, herbs, homeopathics, oils, colloidal silvers, and more natural products protects consumers.

During health care reform negotiations with PhRMA, Waxman feigned concern that drug companies were driving too hard a "bargain" on pharmaceutical prices, but still voted in favor of the cartel's freedom to set their own limits.

Most telling and ironic, PhRMA's official negotiator to whom Waxman complained, "PhRMA should contribute more than PhRMA wants to contribute," was Billy Tauzin, the former congressman who held Waxman's job as chair of the Energy and Commerce committee.

Natural Health News is proud to be a contributing correspondent with the Rense News Network

Tuesday, April 5, 2011

Energy Healing Moves Mountains

UPDATE: 2010
"The greatest discovery that is going to be made is a way of healing two kinds of cancers. However, man must realize that they have to work on body, mind, spirit healing after the cure takes place; else the cancer will make a second call in the same body, for the cure must take place in the mental and spiritual bodies as well as the physical."
From April 2008 -
Over 5,000 years ago, the Yellow Emperor of China, in his Handbook of Internal Medicine, stated that all disease was the result of an imbalance of vital life energies.

Some 30 years ago I signed up for a class in New York, mainly geared to nurses, to learn something called Therapeutic Touch. Delores Kreiger, then at NYU's College of Nursing and Dora Kunz are the founders of the system.

Over the years I have studied and become certified in perhaps five other forms of energy healing. For the most part, I use Reiki (as a Master and teacher) and Kahuna because I enjoy the process and the results I see in people.

I believe in this work to such a degree that I offer Reiki Level One to people by donation rather than charging a high fee as I often see advertised on the web or in a close by city.

The thing is that it does work, and as this story says, you do not have to believe in it to get the benefits.
Healing touch – acupuncture without the needles
Updated: 4/5/2007
By: Ivanhoe Broadcast News

Healing touch therapy is a complementary energy-based approach to healing. The goal of healing touch is to restore balance to the human energy system through a heart-centered relationship with the use of contact and non-contact touch. It is believed this balance can help the body in its natural ability to heal.

While healing touch is an alternative treatment, it is becoming more and more accepted at mainstream hospitals. One hospital that provides healing touch therapy is St. Joseph's Hospital in Tampa, Fla.

Kimberly Gray is the head of the Healing Touch Program there. She's a nurse who has used healing touch for three years with her patients. Her managers, doctors and other nurses started to notice what a difference healing touch had on the patients. So, in 2004, the hospital gave her a chance to do healing touch 100 percent of the time and to track the results of her work.

Gray conducted a study with 140 patients at the hospital. The patients rated their pain, anxiety and nausea before and after the treatment. The study found the average pain score on a scale of zero to 10 decreased from an average of seven before healing touch treatments to two after healing touch treatments.

The data also shows a decrease in anxiety, nausea, and in some cases, a decrease in hospital length of stay-days. The data also shows an increase in overall patient satisfaction. The results were so impressive, the hospital began a healing touch program and named Kimberly as the head of it.

Healing touch is a bio-field therapy. It is described as being similar to acupuncture without the needles. The healing touch practitioner facilitates the healing process by clearing and balancing the bio-electromagnetic field surrounding the human body. The belief is all healing is self-healing, and the balance of energy helps the body achieve the greatest level of ability to heal.

Patients describe the experience as relaxing and a sense of warmth around them. Many patients experience a profound sense of relaxation following a healing touch therapy session.

Kimberly said some of her greatest allies are those who were first skeptical of healing touch therapy. She said with healing touch therapy, the person does not have to believe in it, but they have to be open to the experience. She said that in healing touch, they do not push the energy; they allow energy to flow through them for the greatest benefit to the patient. In her years as a healing touch practitioner, she has seen amazing results from her work. In one case, she helped a young man come out of a coma.
http://www.news8austin.com/content/living/health_beat/Default.asp?SecID=169&ArID=181997&

Monday, April 4, 2011

Saving Billions without Electronic Health Records

The issue of one single set of rules for insurance billing was promulgated in the 1970s. It is now almost 40 years since this was proposed and someone is actually showing what many, including me, have been saying.

Note that is was always Big Insurances that created more layers, more paper, separate paper, and higher cost during this time.
Simpler medical billing saves $7 billion
BOSTON, April 29 (UPI) -- Simplifying and standardizing administrative procedures for medical bills could save about $7 billion a year, U.S. researchers estimate.

Bonnie B. Blanchfield of Massachusetts General Hospital in Boston and colleagues have created a hypothetical model for medical billing that involves a single set of payment rules for multiple payers, a single claim form and standard rules of submission.

If doctors' offices used the streamlined medical billing system they would save 4 hours a week of physician time and 5 hours a week of staff time, Blanchfield said.

The researchers analyzed the billing system of a physician's group affiliated with a large, urban, academic teaching hospital. The researchers found 12.6 percent of submitted claims are initially rejected, but 81 percent are eventually paid -- after using considerable staff time.

"The savings from reducing administrative complexity could be translated into decreased costs in general," the study authors said in a statement. "Mandating a single set of rules, a single claim form, standard rules of submission, and transparent payment adjudication-with corresponding savings to both providers and payers-could provide system wide savings that could translate into better care for Americans."

The findings are published in the journal Health Affairs at http://content.healthaffairs.org/cgi/content/full/hlthaff.2009.0075v1.