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Friday, July 28, 2006

Required Symptoms for a Diagnosis of Chronic Fatigue

Required Symptoms for a Diagnosis of Chronic Fatigue

In March 1988, the CDC released criteria for a diagnosis of CFS; it revised these in 1994 to encompass the broader symptom spectrum of those afflicted. In order to be diagnosed with CFS, a person has to be suffering from these symptoms:

1) New, unexplained, persistent, or relapsing chronic fatigue that is not a consequence of exertion, not resolved by bed rest, and severe enough to significantly reduce previous daily activity; and

2) Four or more of the following symptoms for at least six months:

• Unexplained or new headaches
• Short-term memory or concentration impairment
• Muscle pain
Pain in multiple joints unaccom­panied by redness or swelling
• Unrefreshing sleep
• Postexertion malaise that lasts for longer than 24 hours
• Sore throat
• Tender lymph nodes in the neck or armpits

The Multiple Factors That Contribute to Chronic Fatigue Syndrome

Chronic fatigue syndrome (CFS) is a complicated disorder characterized by profound fatigue that doesn't improve with bed rest and may worsen with physical or mental activity.

Of all chronic illnesses, CFS is one of the most mysterious. Unlike infections, it has no clear cause.

Unlike conditions such as diabetes or anemia, there's essentially nothing to measure. And unlike conditions such as heart disease, there are relatively few treatment options.

The Multiple Factors That Contribute to Chronic Fatigue Syndrome

• Multiple infections (viruses, candidacies, parasites)
Immune dysfunction
Thyroid problems
• Enzyme deficiency
• Toxicity (from environment, food, dental amalgams, and drugs)
• Underlying allergies
• Nutritional deficiency
• Lifestyle (stress, psychological/ emotional factors)
Lyme disease

Preparing measures:

1-3 weeks before the cleaning daily a dandelion on casting take:2 Teaspoon cut up dry dandelion root stick or dandelion sheets with 1 glass cold water to pour over and stand leave 8 hours. Subsequently, the tea is cooked 5-8 minutes and filtered by a filter. Drink mouthful like in the course of the daily.3 days before the cleaning as vegan a nutrition as possible.

The liver cleaning:
They need:4 Spoon epsom salt125 ml olive oil 2 blows grapefruit (you at least 170 needs ml juice.) Often still Ornitin or arginin are recommended. This is not necessary after our experience for success.

The preparing measures described above, which are frequently neglected, are many more important.Accomplish the cleaning best on weekend, so that you can recover on the next day. Execution is most effective with removing moon. Do not take Vitamin or medicines, which do not need you necessarily, in order not to endanger the success of the cure.

To 14,00 o'clock:
Eat fat and protein-free breakfast and lunch (fruit and vegetable; no Dressing etc.). Best you drink only a mixture from carrot, red patch and apple juice.
Starting from 14:00 clock:
Meals and drink you now nothing more (water is permitted).
Around 18:00 clock:
Drink 200 ml water with 1 Spoon epsom salt. (You can the water also before coldly place, thus it more easily drink leave yourselves.)
Around 20:00 clock:
Drink again 200 ml water with 1 Spoon epsom salt.
Around 21:45 clock:
Make your selves finished for the bed. Go also again on toilet.
Around 22:00 clock:
Mix the olive oil with the grapefruit juice well (Shaker). This goes only with freshly pressed juice. Drink the mixture now briskly in standing beside the bed and lie down then immediately! If you do not do this, possibly separate fewer stones, because the liver works much better in lying. Put flat on the back, which head increases somewhat. Additionally you put a hot-water bottle on the liver. Remain so at least 20 minute on the back lying, because the stones separate now. Possibly you feel, how the stones in the liver move. Try to then sleep; also this is important for success.

In the morning:
Drink again 200 ml water with 1 Spoon epsom salt. If you have a stomach detuning, wait to them faded away. Do not drink the solution however before 6 o'clock. They may put now also again to bed. If you have already failure, you can do without the two incomes in the morning.
2 hours later:
Drink for the last time 200 ml water with 1 Spoon epsom salt. After further 2 hours you may begin again slowly to eat. Begin with fruit and light meals.
Examine success:
In the morning you have probably failure. Look in the chair in the toilet for green stones, since they are the proof for it that it concerns Gallstones and not around digesting remainders. Only Galle from the liver is pea green. The chair sinks downward, while the Gallstones swims because of their Cholesterols. Count the brown and the green stones roughly. They should separate altogether several hundred stones, before the liver is well cleaned. For this often 5 cleaning are necessary.

The Gallbladder ways of full Cholesterol crystals, which did not form themselves to round stones, is occasional. They appear as brownish “chaff”, which swims in the toilet on the surface. The elimination of this chaff is just as important as the cleaning of stones.
The cleaning sounds than it is many more complex. Give to your body a chance and judge you then. It will be worthwhile itself for you!!! For individual questions and problems at the time of the execution of the individual points you speak the forum please with your therapist or use you. Please you consider also the non-liability.

Complications like a complete catch were so far not reported

Complications like a complete catch were so far not reported despite 1000facher execution, but conceivable. Therefore one should confer for safety's sake with a therapist. Because straight humans with large stones do not have always also small, visible stones and Galle gries and thus absolutely need a cleaning.For the following problems one should absolutely accomplish a liver cleaning.

The liver cleaning is an effective procedure for the improvement of your well-being. The liver cleaning consists of measures on the day of the cleaning and the preparing measures. The preparing measures serve the effectiveness for the prevention of complications and for the increase, because thereby stones/Gris dissolves already somewhat, so that altogether more stones/ Gris can be separated.

At the time of the execution of a cleaning the front stones/Gris from the large courses are separated and the Gris pieces from the smaller courses into the front, lying farther back, is transported. The courses are simply too long, during an individual cleaning all stones from the innumerable courses could be separated.

Therefore several cleaning are to be accomplished in the distance of one month successively with large complaints, until the complaints disappeared. With a high Cholesterol level so e.g. 3-5 cleaning can be necessary. Only 4 become partial with the 3. or. Cleaning really many stones separated and the complaints improves.

Liver cleansing

Liver cleansing
Did you clean your liver already once? No. Why not? To understand why a liver cleaning is so important, should we the function and the structure of the liver once more exactly look at itself.

The tasks of the liver
The liver
produced over 95% of the blood proteins.
steers the blood sugar content by up and dismantling of glucose (sugar).
regulates the fat metabolism (e.g. Cholesterol)
iron stores
produces the Galle
detoxify the body-own and body-strange material

The above list shows only one excerpt of the most important functions. Altogether the liver is anyhow the most important metabolic organ, i.e. different materials are diminished so over, or that the body can use them. Therefore the liver keeps the blood from the intestine, filled with nutrients, direct. However not only good, but also harmful materials (environmental poisons, preservatives, etc.) with the nutrient-rich blood come into the liver.

The good converted materials are fed over the Vein into the body. The harmful materials are delivered directly over the Gallbladder juice into the intestine, where they are separated with the chair course from the body. The liver is thus also a filter for the nutrient-rich blood. In addition the body in addition, own must “e.g. used” materials like hormones loose will and this happen similarly over the Gallbladder juice of the liver.

The Gallbladder juice serves for however now not only to the decontamination, but also fat digesting in the intestine. The Galle provides for cutting up the fats in our food, so that they can be taken up at all only. The Galle is necessary thus also for the absorption of the fat-soluble Vitamins A, D, E and K.

This Gallbladder juice is formed for large liver small cloths (functional units of the liver) into the 1-2mm. From finest courses, which unite to ever larger, develops a kind tree, whose branches between these liver small cloths begin and become a trunk, which lies outside of the liver and to which Gallbladder way corresponds.

Because of this large Gallbladder way then the Gallbladder is as memory organ. It has the task to collect and deliver if necessary to the intestine the Gallbladder juice, so that we can digest also larger quantities of grease.During the cleaning it concerns to the liver the cleaning of these entire tree-like Gallbladder ways described here!Approx. 25% of all humans over 60 years have visible Gallstones in the Gallbladder or the large Gallbladder way in the ultrasonic.

Here however only the large stones, the so-called Galle gries become visible remain undiscovered.With healthy humans daily approx. 1 liter of Galle flows off by the Gallbladder ways from the liver. The today's civilization human being however has already so clogged Gallbladder ways that often only less than half can flow off. Because already in recent years the liver must eliminate so many Toxins over the Galle that the composition of the Gallbladder juice changes in such a way that Galle gris and Gallstones form.

Particularly the so fine Galle gries already clogs the smallest ways in the liver and obstructs so the discharge. One can compare this with a hose, in which pebbles lie. Since this Galle gries extracts itself however from the modern diagnostics with ultrasonic and Roentgen, he remains also often unconsidered. The fact that however so a handicap in the discharge of the Gallbladder juice has health consequences is clear with the tasks specified above probably everyone. Therefore each humans should pay attention to keep its Gallbladder ways free.

The liver cleaning specified here offers a simple and safe possibility of making the Gallbladder ways free.Note: If you suffered already from Gallstones or to know that large Gallstones is in the courses, it should accomplish you this cleaning only under professional supervision. Because these stones will separate and could lead then to the complete catch. Please you hold always only for consultation with your physician.


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Wednesday, July 26, 2006

Hyperthermia therapy is treatment that uses heat to change or kill cancer cells.

About hyperthermia
Hyperthermia therapy is treatment that uses heat to change or kill cancer cells. Cells are altered when they encounter higher than normal temperatures, making them more susceptible to radiation therapy and chemotherapy. Extremely high temperatures are used to kill cancer cells directly.

Physicians first began to use heat to destroy tumors in the 19th century. For years, the potential cancer-fighting power of hyperthermia was limited by the difficulty in directing heat to the targeted cells without damaging other cells in the body. However, technological advances have made it easier to focus on cancer cells.

Hyperthermia uses heat between 106 to 113 degrees Fahrenheit (41 to 45 degrees Celsius) to treat cancer by one of three main methods:

Local hyperthermia. Also known as thermal ablation, this involves using great heat – up to 113 degrees Fahrenheit (45 degrees Celsius) – to destroy a small area of cancer cells. A square or round box is placed outside the body over the tumor, and forms of energy – including radio waves, microwaves and ultrasound waves – are used to raise the temperature of the target area. The most commonly used technique is radiofrequency ablation (RFA), which uses high-energy radio waves to create the heat.

Regional hyperthermia. Involves raising the temperature of the body or part of the body to a level that is higher than normal through several methods. The heat disrupts the proteins and structures within the cells. This change may allow cancer treatments, such as radiation therapy, chemotherapy or other anticancer drugs, to work more effectively. Regional therapy is used to treat cancer in organs (such as the liver or lung), limbs or body cavities.

Whole-body hyperthermia. Patient receives the heat from warm-water blankets, inductive coils or thermal chambers (similar to large incubators). Increases the effectiveness of chemotherapy in treating cancers that are spreading (metastatic).

At this time, hyperthermia remains largely an experimental procedure. Only about 30 centers in the United States offer the therapy, according to the American Cancer Society.

However, it is being studied in clinical trials to treat some cancers including:

In many cases, clinical trials combining hyperthermia and other cancer treatments have resulted in a significant shrinkage in tumor size. Hyperthermia appears to be particularly effective when combined with radiation therapy. This combination is adept at damaging two types of cells resistant to radiation therapy alone:

Cells in the process of making DNA for replication
Cells that are acidic and poorly oxygenated. Tumors frequently contain cells that are starved for oxygen, and these cells are particularly susceptible to hyperthermia.

The treatment allows the cancer cells to be heated to higher temperatures than nearby healthy cells. Heat also prevents cells from repairing damage caused by radiation, which helps ensure that the initial destructive effect of radiation treatments have longer-lasting effect.

Hyperthermia therapy is the use of heat to damage or kill cancer cells.

Hyperthermia therapy is the use of heat to damage or kill cancer cells. It is used to increase the effectiveness of other cancer treatments, such as chemotherapy or radiation therapy. In some situations, hyperthermia may used by itself to kill cancer cells directly.

Hyperthermia can be delivered via several methods. For the therapy to be effective, the proper amount of heat must be applied to a specific area over a given period of time.

Hyperthermia uses heat between 106 degrees Fahrenheit and 113 degrees Fahrenheit (41 to 45 degrees Celsius) to alter the cancer cells while preventing the surrounding cells from becoming damaged.

At present, hyperthermia therapy is considered to be an experimental procedure and is not widely available. Only about 30 centers in the United States offer this treatment, according to the American Cancer Society.

However, there are many clinical trials under way exploring the use of hyperthermia therapy to treat several types of cancer.

Oberon (device) - From Wikipedia, the free encyclopedia

Oberon (device)
From Wikipedia, the free encyclopedia

Jump to: navigation, search
Oberon or Оберон is a nonlinear computer diagnostics device invented by Russian researchers from the Hospital of Senior Department of Public Health Services of Administration of Omsk Region, led by Vladimir Igorevich Nesterov.

Oberon is a descendant of the original EAV (electroacupuncture) device invented in 1958 by German physician Reinhold Voll, combining Chinese acupuncture with the measurement of galvanic skin differentials.

According to its inventors, Oberon “allows diagnosing not only pronounced pathological processes, but also the earliest forms of the diseases or predisposition to them,” however it “does not belong to the class of medical equipment and consequently does not have to be registered with the committees for certification and licensing of medical-purpose equipment.”
Oberon works with software called Metapathia (Метапатия).

Contents
1 Quotes from Oberon website
2 Related devices
3 Related theories
4 Inventors of related devices and theories
5 See also
6 External links

Quotes from Oberon website

THE LAST WORD IN COMPUTER DIAGNOSTICS
We are glad to welcome you on the official site of the Institute of Applied Psychophysics, the developer of the unique diagnostic device for nonlinear analysis "Oberon", which allows diagnosing not only pronounced pathological processes, but also the earliest forms of the diseases or predisposition to them.

The nonlinear computer diagnostics (NLS) using the device "OBERON" and the program "Metapathia" have been applied at the Hospital of Senior Department of Public Health Services of Administration of Omsk Region since 1999.

The device for telemetric nonlinear analysis data processing "Oberon" was developed by the Institute of Applied Psychophysics, Omsk. The device does not belong to the class of medical equipment and consequently does not have to be registered with the committees for certification and licensing of medical-purpose equipment.

Related devices


Related theories


See also


External links


Retrieved from "http://en.wikipedia.org/wiki/Oberon_%28device%29"

Tuesday, July 25, 2006

What Is Organic? Powerful Players Want a Say

By MELANIE WARNER Customers at McDonald's restaurants in New England are about to get something a little different when they order coffee. Through a deal with Green Mountain Coffee Roasters and Newman's Own, McDonald's will soon be serving a coffee that comes from organic beans and is certified Fair Trade because it meets higher standards in the treatment of coffee workers.

The move, while still a test in a limited region, reflects a much broader trend: The growing interest among large food companies in offering organic foods along with their standard products. General Mills markets the Cascadian Farms and Muir Glen brands; Kraft owns Back to Nature and Boca Foods, which makes soy burgers.

Within the last few years, Dean Foods, the dairy giant, has acquired Horizon Organic and White Wave, maker of Silk organic soymilk. Groupe Danone, the French dairy company, owns Stonyfield Farm. Wal-Mart wants in, too. "We are particularly excited about organic food, the fastest-growing category in all of food,"

Lee Scott, Wal-Mart's chief executive, said at a recent shareholder meeting. "It's a great example of how Wal-Mart can appeal to a wider range of customers." But as organic food enters the mainstream, evolving from an idealistic subculture rooted in images of granola and Birkenstocks, a bitter debate has ensued over what exactly the word "organic" should mean. And now Congress is jumping into the controversy.

With sales of roughly $12 billion, organic food remains a niche market within the $500 billion food industry. But the sector's growing appeal to consumers has fueled a 20 percent annual growth rate in recent years, making it highly attractive to food giants looking for gains in a slow-moving business.

At General Mills, the Cascadian Farms and Muir Glen brands increased sales by 21 percent in the last year, according to the research firm Information Resources Inc., while the company's overall business was up just 1.6 percent. Consumer groups and some organic pioneers say they are concerned that the movement - a response to the practices of corporate food production that promotes a natural chemical-free approach to farming - will become watered down unless firm standards are maintained.

The debate has been under way for several years. But last week, Senate and House Republicans on the Agriculture appropriations subcommittee inserted a last-minute provision into the department's fiscal 2006 budget specifying that certain artificial ingredients could be used in organic food. The Organic Trade Association, an industry lobbying group that proposed the amendment and spent several months pushing for its adoption, says that the measure will encourage the continued growth of organic food.

Some advocacy groups, however, say the amendment will weaken federal organic food standards, first established under a 1990 law. Ronnie Cummins, national director of the Organic Consumers Association, calls the initiative a "sneak attack engineered by the likes of Kraft, Dean Foods and Smucker's."

One of the lobbyists for Altria, Kraft's majority owner, Abigail Blunt - the wife of Representative Roy Blunt, Republican of Missouri, who recently became interim House majority leader after Tom DeLay of Texas resigned from the post - has been working on the issue, the company says. Dean Foods' subsidiary Horizon Organic and the J. M. Smucker Company, the owner of Knudsen and Santa Cruz Organic juices, said they supported the work by the Organic Trade Association, which represents both large and small companies in the business, but did no lobbying on their own.

The amendment injects Congress directly into the debate over whether certain artificial ingredients and industrial chemicals should be allowed in products labeled organic. In a lawsuit ruled upon in January, Arthur Harvey, an organic blueberry farmer, argued that no synthetics at all should be in food bearing the "U.S.D.A. Organic" seal. A federal judge agreed, sending shivers down the spine of many organic food manufacturers. Katherine DiMatteo, executive director of the Organic Trade Association, said that the amendment was intended to protect the industry from the Harvey ruling and will not change the status quo.

If applied, the judge's ruling would have forced many manufacturers to stop using the U.S.D.A. Organic seal and instead relabel products to state, for instance, "cookies made with organic flour" or "frozen lasagna made with organic tomatoes." Many in the organic industry say they are willing to allow some use of synthetics in organic food.

Since 2002, the National Organic Standards Board, a 15-member panel of advisers appointed by the Agriculture Department, has served as the gatekeeper for such substances. In that time, 38 have been approved, many of them relatively harmless ingredients like baking powder, pectin, ascorbic acid and carbon dioxide. But Joseph Mendelson, legal director at the Center for Food Safety, a liberal advocacy group, says that the proposed legislation will open the door to a range of other chemicals and artificial materials, including a large category of so-called food contact substances - things like boiler additives, disinfectants and lubricants with unpronounceable names.

Most of these substances would not end up in finished products in detectable amounts. But many in the organic community say that these tools of mainstream food processing do not belong in organic production. "We don't want organic food manufacturers having carte blanche use of the same kind of synthetics that conventional food processors use, especially when it involves things that do not appear on the ingredient panels," said James A. Riddle, chairman of the National Organic Standards Board. "I think people choose to buy organic food because they don't use all those things."

Ms. DiMatteo contends that the Organic Trade Association is not trying to loosen organic standards or take authority away from the standards board. At the same time, Charles Sweat, chief operating officer at Earthbound Farm, the country's largest grower of organic produce, said he was concerned with the section of the spending bill that gives the Agriculture Department authority to grant temporary exemptions to allow conventionally grown ingredients like corn, soybean oil or tomatoes in organic food when organic versions are not "commercially available." "We see this as opening up a Pandora's box," Mr. Sweat said.

"Any company that can't compete because something is too expensive could go to the secretary and claim they need an exemption." George Simeon, chief executive of Organic Valley, a cooperative of mostly small organic dairy farmers, wrestled with the high cost of organic production a little over a year ago when Wal-Mart asked for a 20 percent price cut. For three years, Organic Valley had been Wal-Mart's primary supplier of organic milk. "Wal-Mart allows you to really build market share," Mr. Simeon said.

"But we're about our values and being able to sustain our farmers. If a customer wants to stretch us to the point where we're not able to deliver our mission, then we have to find different markets." Mr. Simeon told Wal-Mart to get a new supplier. Dean Foods' Horizon Organic was better equipped to satisfy Wal-Mart's demands. Horizon gets about 20 percent of its production from a 4,000-cow organic dairy in Paul, Idaho, which is small in comparison with many conventional dairy farms but huge by organic standards.

Mark Kastel, senior farm policy analyst at Cornucopia, a group representing small dairy farmers, contends that Horizon is able to run such a large farm because it dilutes organic principles. Earlier this year, his group filed a petition arguing that the Idaho farm crams too many cows into a confined area, where most of them do not graze on pasture but instead consume a high-grain diet. "These factory farms are trying to cut corners," Mr. Kastel said. "When you feed more calorie-dense grains, you get more milk." Horizon, which also buys milk from 305 family farms, says it is making changes and will divide its Idaho operation into two separate farms so that there will be three to five cows for each acre of pasture. "We want to meet the regulations," said Kelly O'Shea, Horizon's director of government and industry relations, "and see integrity in the organic standards."

The National Organic Standards Board has been trying to persuade the Agriculture Department to clarify its vague rule that to produce organic milk, dairy cows, besides receiving only organic feed and avoiding growth hormones and antibiotics, must have "access to pasture." It wants to require that milk labeled organic come from cows that get at least 30 percent of their diet from pasture grass for a minimum of 120 days a year.

Mr. Kastel of Cornucopia estimates that roughly 30 percent of the organic milk sold in the United States comes from cows that are not on pasture, most of them from two large dairies run by Aurora Organic Dairy, an offshoot of what was once the country's largest conventional dairy company. Organic milk is the most popular organic product and sells for up to twice the price of regular milk. On a recent visit to Aurora's farm in Platteville, Colo., at the foot of the Rocky Mountains, thousands of Holsteins were seen confined to grassless, dirt-lined pens and eating from a long trough filled with 55 percent hay and 45 percent grains, mostly corn and soybeans. Of the 5,200 cows on the farm, just a few hundred - those between milking cycles or near the end of their lactation - were sitting or grazing on small patches of pasture. Aurora executives say that despite the lack of pasture, their cows are "very healthy and happy."

The 10 million gallons of milk the farm produces each year are supplied mainly to supermarkets and sold under store brands like Safeway Select, Kirkland at Costco and Archer Farms at Target. Mark Retzloff, president of Aurora Organic, said he did not agree with the National Organic Standards Board's proposed pasture rule, but added that he was planning to add 550 acres of grazing land to the farm.

The company is also building a new dairy in a layout that Mr. Retzloff said would be conducive to putting thousands of cows on pasture and still milking them three times a day. Such tensions are likely to remain whatever the new legislation allows. Sheryl O'Laughlin, chief executive of Clif Bar, which makes organic energy bars, says that while the difficulty of operating organically and finding natural ingredients often ends up raising production costs, it is also what gives the category its purity and its appeal. "The organic industry," Ms. O'Laughlin said, "has got to put pressure on itself to find alternative solutions."

Exercise and healthy diet slow memory loss

By Paul Hoskins An active lifestyle and a healthy, fish-rich diet are not only good for your heart, they may also help tackle the memory loss associated with old age, two leading neuroscientists said on Wednesday.

As people live longer, finding ways of halting the decline in mental agility is becoming increasingly important, said Professor Ian Robertson, director of the Institute of Neuroscience at Trinity College Dublin.

"The biggest threat to being able to function well and properly is our brains," he told journalists at the British Association for the Advancement of Science meeting in Dublin. "There is very strong evidence, particularly in the over-50s, that the degree to which you maintain your mental faculties depends on a handful of quite simple environmental factors," he said, having identified seven key areas.

Those who remained physically fit, avoided high stress levels and enjoyed a rich and varied social life are better equipped to stay alert as they age. Mental stimulation, learning new things and simply thinking young also help. A new survey compiled for the University of Kent and the charity Age Concern showed ageism was rife in Britain where people, on average, see youth as ending at 49 and old age beginning at 65.

But Robertson said such attitudes were not helpful given the number of 80-year-olds who remain "sharp as pins." "If you start to think of yourself as old when you are 60, which is no longer justified, you will behave old," he said. GOOD FOR YOUR BRAINS Research conducted by his Trinity College colleague Professor Marina Lynch showed healthy eating was another key requirement for staying on the ball, according to Robertson.

Lynch said new research showed fish oils may reduce the cell inflammation that triggers a decline in memory. "Studies have identified the anti-inflammatory properties as well as the restorative qualities of omega-3," she said of the essential fatty acid found in supplements like cod liver oil and fatty fish such as mackerel, salmon and tuna.

Already believed to protect the brain against the damage caused by Alzheimer's disease, omega-3 has also been linked with maintaining healthy hearts and joints. Lynch said the biggest surprise of the latest discovery was that omega-3 appeared not only to replace anti-inflammatories that dwindle with age but also to stem a corresponding rise in chemicals that cause the cell inflammation in the first place.

"These effects seem to cobble together to restore the ability of people to maintain memory as they grow older," she said, pointing to a study by the University of Aberdeen showing a diet rich in fatty fish slowed the brain's aging process.

Vitamin users in last-ditch bid to stop ban on supplements

By Geoffrey Lean and Steve Bloomfield 23 January 2005 Consumers and producers of popular vitamin and mineral supplements used by thousands every day will this week make a last-ditch attempt to prevent a European Union directive from banning them. Campaigners claim products from well-known brands including Holland and Barrett, Solgar and Viridian will be removed from the shelves unless they are reformulated.

The campaign against the directive has enlisted the help of a number of high-profile supporters, including Cherie Blair's former lifestyle adviser Carole Caplin and the actress Jenny Seagrove. Dame Judi Dench and Bianca Jagger are also backing the campaign. A third of women and a quarter of men take health food supplements in the UK and the market is thought to be worth at least £350m a year.

The EU directive lists only 28 vitamins and minerals, and 112 sources from which they were derived for use in food supplements, which can be sold legally after it comes into force on 1 August. It would threaten up to 5,000 products, containing more than 200 nutrients, which campaigners claim have been used safely in specialist supplements for many years. Some large chains, such as Boots, have already reformulated their products to meet the new EU rules and say their customers will see no difference when the directive comes into force.

Also, manufacturers who submit detailed scientific dossiers by July this year that prove their ingredients are safe will still be allowed to sell their products. Campaigners say the cost on suppliers could force smaller firms into bankruptcy. Few of the small health food companies can manage the expense - up to £250,000 for each ingredient - and only a handful of safety dossiers are being prepared. Consumers for Health Choice, who have been leading the campaign against the directive, said that products under threat include Solgar Prenatal Nutrients, which contain nutrient sources not on the EU's list, and Holland and Barrett's ABC Plus, which has a high dose of vitamin C.

A court case brought by the National Association of Health Stores and the British Health Foods Manufacturers Association will argue on Tuesday that Brussels is exceeding its powers by imposing a blanket ban. It is being contested by the EU's institutions and by the governments of Greece and Portugal as well as Britain. On the same day, the Conservatives, who say the measure will outlaw virtually every popular multi-vitamin pill sold in the country, will call in the Commons for the ban to be scrapped.

Ministers are concerned that growing public opposition to the ban will affect the referendum on the European Constitution, due after the general election. Peter Hain, the Leader of the House of Commons, has called it "unnecessary interference" by Brussels, and other ministers have privately expressed sympathy with the protesters. But the Government is still pressing ahead with the ban, and will defend it in the European Court case. Some reports suggest that some products could cause problems in high doses, but a major body of research demonstrates that deficiencies in minerals and vitamins, levels of which are falling in modern diets, can cause heart disease, osteoporosis, cancer and other conditions.

A recent study published by the American Medical Association shows that taking some mineral and vitamin pills reduces the risk of contracting cancer and cardiovascular disease, and protects foetuses. The ban, the first of a series of EU measures designed to outlaw a range of alternative medicines, is contained in the Food Supplements Directive, passed in 2002 to harmonize the trade in supplements between EU member states and after lobbying from the pharmaceutical industry. Sue Croft, a spokeswoman for Consumers for Health Choice, said: "If this directive comes into force it will affect the lives of millions. T

o have these supplements removed and to put more strain on the NHS is nothing short of a crime. At the election we will be targeting those MPs who do not vote to stop this." A spokeswoman for Boots, however, which has a third of the vitamin supplement market, said the company had been gradually reducing the level of vitamins and minerals in own-brand supplements in line with new safety levels. "Consumers won't see a huge change," a spokeswoman said. "We fully support this EU directive."

FDA Considers Warnings for Eczema Creams

By Rob Stein Washington Post Staff Writer Saturday, February 12, 2005 Government scientists, concerned that two prescription creams used widely for a common skin condition may increase the risk of certain cancers, especially among children, will propose adding strong new warnings to the product labels. A handful of cases of cancer have been reported among adults and children using the creams, sold under brand names Elidel and Protopic, and animal and laboratory studies suggest the drugs could be to blame, according to a new Food and Drug Administration analysis.

"The evidence raises serious safety concerns in children regarding the potential for carcinogenicity in humans treated with these agents," wrote Jean Temeck of the FDA's division of pediatric drug development in a recommendation posted late yesterday on the agency's Web site. The document was one of several posted in preparation for a meeting of an expert panel next week to assess the safety of the creams and recommend what action the agency should take. Protopic and Elidel were approved in 2000 and 2001, respectively, to treat eczema, a common, chronic skin condition that causes redness and itching.

Before the new creams, the only treatment had been steroid creams and ointments, which can be used only for short periods and can have a variety of side effects. The new creams, which were seen as effective and much safer, immediately became popular. At least 5 million prescriptions have been written for the creams. The creams were approved for short-term or intermittent use by adults and children age 2 and older, but Novartis Pharmaceuticals Corp. has marketed Elidel aggressively, and both creams are believed to be widely used for longer periods and among babies. "These products are being widely used to treat . . . a non-life-threatening disease, and heavily advertised for use in young children without appreciation . . . regarding the potential for carcinogenic risk," Temeck wrote.

Both Novartis and Fujisawa Healthcare Inc., which makes Protopic, defended the safety of their products to the FDA. "Elidel is an effective, steroid-free treatment for mild to moderate eczema and has a well-established safety profile," Novartis spokesman Tom Jones added in an e-mail. Because the drugs work by suppressing the immune system, scientists had been concerned that they could increase the risk of cancer.

As a result, when the FDA approved the creams the agency required both companies to monitor whether any cancers were reported among users. In 2003, the agency convened an expert panel to examine the evidence to date, but at that time only seven possible cases had been reported, so the agency decided to continue to monitor the situation. Since then, however, a study involving monkeys has suggested the creams might cause lymphoma, a cancer of the immune system, and reports of a variety of cancers in humans using the creams have continued to rise. At least seven cases of lymphoma have been reported, as well as at least seven cases of skin cancer and a handful of others, Temeck wrote.

Several children reported infections, including an 8-month-old boy whose infection was so severe he suffered a heart attack after Protopic was applied "over his entire body for six months," she wrote. While it remains far from proven that the creams are causing the complications, "there is a need for a stronger approach to the communication and minimization of the potential risk of cancer," Dianne Murphy, director of the FDA's office of pediatric therapeutics, wrote in another document. "We believe regulatory action is needed at this time since a definitive answer to the carcinogenic risk of these products will not be known for years," Temeck wrote. The addition of a possible "black box" warning to the label is one of several recommendations that the committee will consider, an agency spokesman said.

The concern comes as the FDA has come under intense criticism for failing to protect the public from potentially dangerous drugs. The blockbuster painkiller Vioxx was recently pulled from the market because of concerns that it and similar agents may increase the risk of heart attacks and strokes. The advisory committee will focus on children because exposure to a potential cancer-causing agent poses a greater risk to the young, but its recommendations would apply to adults as well, the spokesman said. Although the FDA is not bound to follow the recommendations of its advisory panels, it usually does.

Sunday, July 23, 2006

"Dr Ozone" denies wrongdoing

Jul 13, 2006
An Austrian man accused of luring terminally ill foreigners to Thailand with promises of a miracle cancer cure says he's done nothing wrong, and the husband of a dead Australian patient agrees.
Hellfried Sartori spoke to AAP through jail cell bars at a police station in the northern Thai city of Chiang Mai, where he has been held since his arrest on Sunday.
"I have not committed any crime.

All I did was to try to help people after they approached me," he said as police investigations into his therapies were underway in Thailand, the Northern Territory and Western Australia.
"And I gave free advice to many people, including some in Australia, to try to assist them back to a healthy life."

Sartori, 67, was stripped of his medical licence in several states in the United States, where Thai police say he has served jail time.
Thai police said Sartori was expected to face court on Saturday on charges of fraud and impersonating a doctor, offences that carry five years imprisonment.

Sartori insisted he was still a registered physician in some parts of the world. However in Thailand he had acted only as a "technician" while nurses injected patients with chemicals.
In Darwin today the widower of Australian ovarian cancer patient Kathleen Preston, who died in Thailand two years ago after being treated by Sartori, said there was nothing for police or the NT Coroner to investigate.

"There's nothing wrong," said Keith Preston, who instead accused the Australian medical system of failing his wife.
As well as receiving the "natural" treatment in Thailand, Preston also travelled to Singapore and Mexico for help.
"You won't get anything done in Australia," Preston said."They tell you to go home and die. They weren't doing anything.
Meanwhile, Western Australian police named Sartori and Perth physician Dr Alexandra Boyd as persons of interest over the deaths of six terminally ill people who were given cesium chloride therapy in Perth in May 2005.

Detective Sergeant Terry Rackich said the cancer patients had paid "tens of thousands" of dollars for treatment.

The six Australians as well as one New Yorker were allegedly treated at Boyd's home because Sartori could not get a visa. Within two days four were dead and two died within a month.
Sergeant Rackich said: "We're looking at any aspect of any criminality that has occurred but at this particular point in time it is just going to be referred to the coroner."
He said Boyd had declined to be interviewed by police.

In a statement tonight, Boyd said neither she nor her clinic had administered "any cancer treatment to these Perth-based patients of Mr Sartori" but had ordered and reviewed blood tests for some of them.

Inside Chiang Mai's jail, Sartori lashed out at the Maharaj Nakhon Chiang Mai Hospital where Preston died soon after undergoing his controversial "ozone treatment".
Sartori said Preston flew to Thailand with her husband to be diagnosed and was given what Sartori said were "special injections".

"That poor woman bled to death because of the incompetence of the staff at that hospital," Sartori said.

"I intend to sue them for $US20 million ($A27 million) as soon as I get out of here."

A Thai post-mortem examination found excessive potassium in her blood.
Sartori said he had not been interviewed by Australian Federal Police.

Thai police said they were investigating the deaths of other patients under Sartori's care.
Detectives said Sartori, who studied medicine in his native Austria, was convicted in the US of illegally administering his so-called "ozone treatments", and was jailed in New York State in May 1992 and Washington DC in July 1998.

Sartori admitted today that he had charged his "patients" $A50,000 for his treatments, which were carried out in hotel rooms in and around Chiang Mai.

"How can they accuse me of impersonating a medical practitioner?" he said.
"I was licensed by the General Medical Council of the United Kingdom in 1992 - and I still hold that valid licence today."
Sartori also claims his 40-year-old medical qualifications from Graz University in Austria remain valid under European Union law.

He said he had lived in Thailand for 10 years "on and off" and that he had visited Sydney, Melbourne, Perth and Darwin "a number of times" - although he refused to be specific about the dates and purpose of these trips.

"At all times during my work with people who came to see me here, their own relations were present at every stage of the treatment," Sartori said.

One of Sartori's patients, New Zealander Melissa Judith Taylor, lost consciousness during treatment in Chiang Mai last month. She has since returned home.

Source: AAP

Health Highlights: May 7, 2006

Here are some of the latest health and medical news developments, compiled by editors of HealthDay:
CDC Reports More Eye Fungus Infections
U.S. health officials said the number of confirmed cases of a rare eye fungus that can cause scarring of the cornea has climbed to 102. But the source of the infection linked to contact lens cleaners remains unknown, the Associated Press reported.
Bausch & Lomb Inc. stopped U.S. sales of its ReNu with MoistureLoc contact-lens solution on April 10 when the federal Centers for Disease Control and Prevention said it was investigating numerous reports of Fusarium keratitis infections in Americans using the product.
The proportion of patients who said they used MoistureLoc has held steady at around 50 percent to 60 percent of the cases confirmed so far, the CDC said. Other patients have reported using other ReNu brands and six said they used cleaners made by Alcon Inc. and Advanced Medical Optics Inc., the AP reported.
"At this point, it is too early in the investigation to say whether a particular product or solution may be responsible for the outbreak," the CDC said in a statement.
-----
U.S. Buys More Anthrax Vaccine
The U.S. Department of Health and Human Services said it has purchased five million additional doses of Anthrax Vaccine Adsorbed (AVA), a licensed anthrax vaccine, for $120 million.
This supply of AVA anthrax vaccine, from the BioPort Corporation of Lansing, Mich., is in addition to the five million doses of AVA vaccine purchased from BioPort last year. It will be kept in the nation's Strategic National Stockpile, where it will be available in the event of a bioterror anthrax attack, HHS said in a statement released Friday afternoon.
Coupled with an existing supply of antibiotics -- the nation's first line of defense against an anthrax attack -- the additional AVA vaccine should further diversify the nation's stockpile of medical treatments, the statement said.
"We are committed to protecting the nation from the consequences of an anthrax attack," said Stewart Simonson, HHS assistant secretary for public health emergency preparedness.
-----
New Guidelines for Cancer Therapy
The American Society of Clinical Oncology has developed revised guidelines for the use of white blood cell growth factors -- also known as hematopoietic colony stimulating factors, or CSFs -- to prevent a potentially dangerous side effect from cancer treatment called febrile neutropenia.
White blood cell growth factors are proteins that help the body produce the white blood cells that help fight infection. Some cancer treatments can destroy white blood cells, leading to a condition called neutropenia. Febrile neutropenia -- or neutropenia with a fever -- is a dangerous condition that often requires hospitalization.
ASCO's 2006 Update Committee agreed that reduction in febrile neutropenia is an important goal that justified the use of CSFs when the risk of febrile neutropenia is 20 percent or higher, and no other effective chemotherapy regimen with a risk of febrile neutropenia lower than 20 percent is available. The previous guideline had recommended CSF use when the risk of febrile neutropenia was 40 percent or higher, the society said in a prepared statement.
"CSFs are supportive medications, which means they are not intended to treat the cancer, but rather to prevent patients from developing dangerous side effects from cancer treatment," said Dr. Thomas J. Smith, lead author of the guidelines and a medical oncologist with Virginia Commonwealth University's Massey Cancer Center.
The guidelines also include new recommendations for the use of CSFs for patients receiving radiation treatment and for older patients; and updates on recommendations for patients with specific diseases, such as acute leukemia and myelodysplastic syndromes, and for pediatric patients.
-----
FDA Issues Warning on Bowel-Cleansing Products
The U.S. Food and Drug Administration warned Friday of potential kidney failure associated with certain products used to clean the bowel before colonoscopies and other procedures, the Associated Press reported.
Agency officials, in an alert to doctors and patients, said they had documented 22 cases of acute phosphate nephropathy, a rare but serious form of kidney failure linked to the use of oral sodium phosphates. The products cleanse the bowel by causing patients to loose large amounts of fluid through bowel movements, the AP said.
Twenty-one of the cases involved patients given products such as Fleet Phospho-soda or Fleet Accu-Prep. One patient had taken Visicol tablets. None had taken OsmoPrep tablets, a recently approved oral sodium phosphate product, the FDA said.
-----
No Aspartame-Cancer Link, Says Expert Panel
The popular artificial sweetener Aspartame does not increase the risk of cancer, an independent panel of European food-safety experts said Friday.
They reviewed an Italian study released last year that concluded that aspartame was linked to higher rates of lymphoma and leukemia in rats. But the expert panel for the European Food Safety Authority said the number of tumors did not increase in relation to the amount of aspartame given to the rats, the Associated Press reported.
Many of the rats used in the Italian study had suffered from chronic respiratory disease, which was the most likely cause of the tumors, the panel concluded.
"There is no reason ... to undertake any further extensive review of the safety of aspartame," said toxicologist Iona Pratt, who headed the panel.
The findings come a month after the release of a study of half a million Americans that found no link between aspartame and cancer, the AP reported.
Aspartame is used in thousands of products, including chewing gum, sodas, and many medicines.
-----
California Bill Targets Personal Use of Ultrasound Machines
Call it Cruise Control: The California Assembly voted 55-7 in favor of a bill to restrict the sale of ultrasound machines only to licensed professionals, a move meant to prevent personal use of the medical devices.
The bill, which now moves to the Senate, was introduced after movie star Tom Cruise bought an ultrasound machine to see images of his unborn daughter, who was born last month in Los Angeles, the Associated Press reported.
Doctors criticized Cruise for his actions, noting that improper use of ultrasound can harm a fetus. Technologists and doctors typically receive years of training to conduct ultrasound exams.
The U.S. Food and Drug Administration says laboratory tests have shown that certain diagnostic levels of ultrasound can affect human tissue, the AP reported.

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Health Highlights: May 6, 2006

Here are some of the latest health and medical news developments, compiled by editors of HealthDay:

U.S. Buys More Anthrax Vaccine
The U.S. Department of Health and Human Services said it has purchased five million additional doses of Anthrax Vaccine Adsorbed (AVA), a licensed anthrax vaccine, for $120 million.
This supply of AVA anthrax vaccine, from the BioPort Corporation of Lansing, Mich., is in addition to the five million doses of AVA vaccine purchased from BioPort last year. It will be kept in the nation's Strategic National Stockpile, where it will be available in the event of a bioterror anthrax attack, HHS said in a statement released Friday afternoon.
Coupled with an existing supply of antibiotics -- the nation's first line of defense against an anthrax attack -- the additional AVA vaccine should further diversify the nation's stockpile of medical treatments, the statement said.
"We are committed to protecting the nation from the consequences of an anthrax attack," said Stewart Simonson, HHS assistant secretary for public health emergency preparedness.
-----
New Guidelines for Cancer Therapy
The American Society of Clinical Oncology has developed revised guidelines for the use of white blood cell growth factors -- also known as hematopoietic colony stimulating factors, or CSFs -- to prevent a potentially dangerous side effect from cancer treatment called febrile neutropenia.
White blood cell growth factors are proteins that help the body produce the white blood cells that help fight infection. Some cancer treatments can destroy white blood cells, leading to a condition called neutropenia. Febrile neutropenia -- or neutropenia with a fever -- is a dangerous condition that often requires hospitalization.
ASCO's 2006 Update Committee agreed that reduction in febrile neutropenia is an important goal that justified the use of CSFs when the risk of febrile neutropenia is 20 percent or higher, and no other effective chemotherapy regimen with a risk of febrile neutropenia lower than 20 percent is available. The previous guideline had recommended CSF use when the risk of febrile neutropenia was 40 percent or higher, the society said in a prepared statement.
"CSFs are supportive medications, which means they are not intended to treat the cancer, but rather to prevent patients from developing dangerous side effects from cancer treatment," said Dr. Thomas J. Smith, lead author of the guidelines and a medical oncologist with Virginia Commonwealth University's Massey Cancer Center.
The guidelines also include new recommendations for the use of CSFs for patients receiving radiation treatment and for older patients; and updates on recommendations for patients with specific diseases, such as acute leukemia and myelodysplastic syndromes, and for pediatric patients.
-----
FDA Issues Warning on Bowel-Cleansing Products
The U.S. Food and Drug Administration warned Friday of potential kidney failure associated with certain products used to clean the bowel before colonoscopies and other procedures, the Associated Press reported.
Agency officials, in an alert to doctors and patients, said they had documented 22 cases of acute phosphate nephropathy, a rare but serious form of kidney failure linked to the use of oral sodium phosphates. The products cleanse the bowel by causing patients to loose large amounts of fluid through bowel movements, the AP said.
Twenty-one of the cases involved patients given products such as Fleet Phospho-soda or Fleet Accu-Prep. One patient had taken Visicol tablets. None had taken OsmoPrep tablets, a recently approved oral sodium phosphate product, the FDA said.
-----
No Aspartame-Cancer Link, Says Expert Panel
The popular artificial sweetener Aspartame does not increase the risk of cancer, an independent panel of European food-safety experts said Friday.
They reviewed an Italian study released last year that concluded that aspartame was linked to higher rates of lymphoma and leukemia in rats. But the expert panel for the European Food Safety Authority said the number of tumors did not increase in relation to the amount of aspartame given to the rats, the Associated Press reported.
Many of the rats used in the Italian study had suffered from chronic respiratory disease, which was the most likely cause of the tumors, the panel concluded.
"There is no reason ... to undertake any further extensive review of the safety of aspartame," said toxicologist Iona Pratt, who headed the panel.
The findings come a month after the release of a study of half a million Americans that found no link between aspartame and cancer, the AP reported.
Aspartame is used in thousands of products, including chewing gum, sodas, and many medicines.
-----
California Bill Targets Personal Use of Ultrasound Machines
Call it Cruise Control: The California Assembly voted 55-7 in favor of a bill to restrict the sale of ultrasound machines only to licensed professionals, a move meant to prevent personal use of the medical devices.
The bill, which now moves to the Senate, was introduced after movie star Tom Cruise bought an ultrasound machine to see images of his unborn daughter, who was born last month in Los Angeles, the Associated Press reported.
Doctors criticized Cruise for his actions, noting that improper use of ultrasound can harm a fetus. Technologists and doctors typically receive years of training to conduct ultrasound exams.
The U.S. Food and Drug Administration says laboratory tests have shown that certain diagnostic levels of ultrasound can affect human tissue, the AP reported.
-----
Kaiser Permanente Bungled Kidney Patient Transfers: Report
U.S. regulators were overwhelmed and some patients lost out on new kidneys after Kaiser Permanente launched a massive, new kidney-transplant program in 2004, the Los Angeles Times reported.
The HMO started the program without first discussing with regulators how to safely transfer up to 1,500 of Kaiser Permanente's patients to its San Francisco center from two medical centers -- UC San Francisco and UC Davis -- where they were receiving care paid for by Kaiser.
Officials with the United Network for Organ Sharing told the Times that they weren't informed about the need to move hundreds of kidney patients until September 2004, after Kaiser had already opened its new kidney-transplant program. The United Network is the federal contractor that oversees the U.S. transplant system.
The poor planning and paperwork led to long delays in hundreds of patient transfers. Many patients weren't informed that their transfers had not been processed, which effectively put a new kidney out of reach, the Times reported.
Earlier this week, the newspaper reported that 56 transplants had been performed at Kaiser's transplant center, but about twice as many patients on the waiting list had died.
Kaiser has launched an investigation and will not comment until it's complete, a spokesman said.


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Saturday, July 22, 2006

Colon Hydrotherapy Course

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Colon Hydrotherapy Certification Course 45 hours (6 Days) with Certificate

We provide monthly presentations on CAM (complementary and alternative) therapies to students and faculty in order to facilitate the understanding of these therapies in an integrative model of healthcare.

Course outline
The Digestive Tract
The Digestive System and How it Works
What is Colon Hydrotherapy?
Historical View of Colon Irrigation
Common Concerns about Colon Irrigation
Colon Hydrotherapy Equipment
Basics Live Blood Analysis
Basics Ozone Oxygen Therapy
Basics Electro frequency - Dr. Royal Rife
Basics Zapper
Cleaning and Sanitation of Equipment
Pre-Treatment Client Interview
Indications and Contraindications
Colon Hydrotherapy in Disease Prevention
Operation and Treatment Procedure
Use of Oxygen
Practical Application Colonic Treatments
Digestive Diseases
Digestive Diseases Statistics
The Digestive Disease Dictionary
Diagnostic Tests
Reactions to Colon Hydrotherapy Treatments
Parasites of the Intestinal Tract
Prevention of Disease Transmission
Other Helpful Tools for Colon Hydrotherapy
Therapeutic Implants
X-ray Readings and Barium Enemas

Additional Recommended Reading
The course consists of 2 parts: 20 to 60 hours of pre-study (depending on your existing knowledge of anatomy & physiology and 45 hours (6 Days) of study in our teaching facilities (approx. 20 hours of theoretical presentations and 25 hours of practical treatment exposure). As a student enrolling for this course, you are required to study the course material before attending the 2nd part at our teaching facilities. At the end of the course a written multiple choice examination needs to be completed by each student. Graduates of this course will receive a Certificate.


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Friday, July 21, 2006

Study Compares Treatments for Kids' Lung Infection

(HealthDay News) -- Doctors say they've come up with a cheaper but equally effective means of battling an infection of the lining of the lungs in children.

The treatment, which involves the use of enzyme urokinase to help drain the chest, costs 25 percent less than video-assisted thorascopic surgery and should be the primary treatment for this condition, known as empyema, according to a British team reporting in the July issue of the American Journal of Respiratory and Critical Care Medicine.

Both treatments provide equal clinical results, said the researchers, who studied 60 children with empyema. The condition involves pus from pneumonia infecting the pleural membrane that lines the lung walls.

For this study, 30 of the children (average age 3.5 years) were treated with chest drainage using intrapleural urokinase and the other 30 children underwent video-assisted thorascopic surgery.

"The aim of treatment is empyema is to sterilize the pleural cavity, reduce fever and ensure the full expansion of the lung so it can return to normal function," researcher Dr. Samantha Sonnappa, of the Portex Respiratory Unit at the Institute of Child Health in London, said in a prepared statement.

"Our study is the first randomized prospective trial to compare chest drain against primary video-assisted thoracopic surgery for the treatment of empyema in children."

The two treatment groups had no significant clinical differences in terms of length of hospital stay, failure rate of the procedure, or radiologic outcome at six months after treatment.

"An important observation is that video-assisted thorascopic surgery is $2,250, or 25 percent, more expensive than intrapleural urokinase at our center without including start-up costs for the provision of surgery," Sonnappa said.

An accompanying editorial in the same issue of the journal expressed some concerns about the study.

"One would certainly say that, on a cost basis, urokinase is the better choice if the therapies are equivalent in every other way," wrote Dr. Julian Allen and Dr. Peter Mattei of the Children's Hospital of Philadelphia and the University of Pennsylvania School of Medicine.

But they noted that study data seems to suggest that children in the surgical study group may have had slightly worse disease than those receiving urokinase, potentially skewing the results. In addition, certain clinical factors were not reported by the study authors, which means there could have been even more differences between the two treatment groups.

"Other important outcomes include the following: the amount of pain associated with the intervention and long-term physiologic outcomes such as pulmonary function and exercise tolerance. These variables are certainly more important than a $2,000 difference in cost," the editorial authors wrote.

More information
The U.S. National Library of Medicine has more about empyema.
Last reviewed: 07/18/2006 Last updated: 07/18/2006

Breast-Feeding Eases Baby's Pain During Tests

WEDNESDAY, July 19 (HealthDay News) -- Breast-feeding can ease the pain experienced by newborns during routine heel-prick or needle-stick blood tests, Canadian researchers report.

The researchers analyzed data from more than 1,000 newborns in 11 studies that compared the effectiveness of breast-feeding and breast milk to sugar water or a pacifier in easing the discomfort experienced while the blood samples were taken from infants.

"The babies who were breast-fed experienced less pain, compared to not giving anything, or just swaddling them or a placebo of sterile water," lead reviewer Prakeshkumar Shah, a neonatologist at Mount Sinai Hospital in Toronto, said in a prepared statement.
Breast-feeding and sugar water were about equally effective in reducing pain.

The reviewers said it's unclear how breast-feeding may help reduce the pain, although a number of factors -- the mother's comforting presence; skin-to-skin contact; diversion of the baby's attention; and the sweetness of breast milk -- probably play a role.

The use of any kind of pain relief for this procedure varies from hospital to hospital, Shah noted. Some health workers and parents don't believe that the procedure causes enough pain to require pain relief.

The review findings also suggest that breast-feeding may offer a natural method of pain relief for premature babies, who often have to undergo many painful procedures, Shah said.
"Right now, quite a lot of hospitals have adopted the practice of giving sugar water to those babies for analgesia. But we don't know what happens to them long term by exposing them to high concentrations of sugar," Shah said.

"I think more research is needed on the effectiveness of breast-feeding and breast milk for those babies," he said. "What we are proposing in this review is to do further research on those sick babies that are admitted to the (neonatal intensive care) unit who are exposed to multiple painful procedures."

The findings are published in the current issue of The Cochrane Library.

More information
The U.S. National Library of Medicine has more about newborn screening tests.
Last reviewed: 07/19/2006 Last updated: 07/19/2006

Steamy Air Won't Ease Croup

WEDNESDAY, July 19 (HealthDay News) -- Contrary to popular belief, humid air does not relieve the coughing and wheezing of croup in children, a new study shows.

"Typically, you get people to run a hot bath or shower in the bathroom. Or you get them to boil a kettle in the room, or have hot water in the corner of the room. That's the kind of first-aid advice that is often given at the point of first contact with a health-care professional," lead reviewer Dr. Michael Moore, a family doctor at Three Swans Surgery in Salisbury, England, said in a prepared statement.

In the study, published in the current issue of The Cochrane Library, Moore and his colleagues analyzed data from three studies of 135 children with croup who were seen in a hospital emergency department.

The outcomes for children treated with moist air did not differ significantly from those who received no treatment, the researchers found.

"We haven't shown any benefit from using the moisturized air in the emergency department, and there's no particular reason to think that it would work better at home," Moore said.
Croup, usually caused by a viral infection, leads to swelling in the upper part of the airway and affects the voice box. Because they have narrower airways than older children and adults, young children are especially susceptible to croup.

"I think that probably the successes that were attributed to humidity in the past were due to the calming effect of the parent believing that they were doing something, the child taking deeper breaths, the child getting over the spasmodic element of the croup, and then just getting better," Dr. Dennis Scolnik, an emergency room pediatrician at The Hospital for Sick Children in Toronto, Canada, said in a prepared statement.

"I think humidity probably wouldn't harm. But I think it's a false sense of security," he added.
There are medical treatments for serious cases of croup, he added.

More information
The Nemours Foundation has more about croup.
Last reviewed: 07/19/2006 Last updated: 07/19/2006

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