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A Remarkable New Treatment for Chronic Fatigue, Fibromyalgia, and Other Chronic Diseases -- A Fraud!

Radiant Health Medical Center, in the north Bay area.Dr. Robert Jay Rowen, a Phi Beta Kappa graduate of Johns Hopkins University and graduate of the University of California, San Francisco School of Medicine is internationally known for his work in the field of complementary/alternative/integrative medicine. He is affectionately known as the “Father of Medical Freedom” for pioneering the nation’s first statutory protection for alternative medicine in 1990 in Alaska, against a concerted opposition from the organized medical community and an imported “quackbuster”. A few years later, the Alaska governor appointed him to a term on the state medical board against overwhelming opposition from the medical establishment. His appointment was ultimately confirmed by the legislature with overwhelming public support. The rare medical freedom he enjoyed in Alaska enabled him to greatly expand knowledge and experience in a multitude of disciplines and therapies not normally found in medicine. Jumping into alternative medicine in 1983 through a practice in acupuncture, he quickly expanded to nutritional medicine, chelation therapy, oxidation therapy, homeopathy and herbal medicine, and took intensive training in neural therapy and prolotherapy to help treat and eliminate acute and chronic pain. Alaska’s laws enabled him to work extensively with innovative cancer therapies, ozone, and ultraviolet blood irradiation therapy. He is internationally known and respected for training hundreds of open-minded physicians in these techniques from around the world.
In 2001, he became editor in chief of Second Opinion, one of the nation’s leading monthly publications revealing the frontiers of medicine. Thus, he reduced his practice load considerably to write and teach, and relocated from Alaska to California where he works part time with his like minded talented wife, Terri Su, MD at her Santa Rosa office,
Article
Susan had suffered with chronic fatigue, pain, and mental aberrations for several months. The pain was so intense it was making it impossible to perform her daily tasks. Her doctor ran a series of tests on her, but was unable to find anything wrong. When she returned several times complaining of the same problems, he told her she was a psychiatric case and needed to see a specialist.
[Karl Note: The most usual "remedy" for fibromyalgia is a psychiatric drug. They don't work, but the psychs keep trying!]
Susan wasn’t crazy — she had fibromyalgia. And she’s not alone in her suffering. Over the past two generations, we’ve seen a startling rise in all kinds of chronic health problems. These include (but are not limited to):
chronic fatigue, fibromyalgia, arthritis, autoimmune diseases (so-called), vascular disease, endocrine (hormone) problems, infertility, and more.
These problems are so rampant now that if you don’t suffer from one of them, you likely know someone who does.
These chronic problems are the number one reason people visit the doctor. But the doctor can’t do anything to help. What you are about to read, though, is one of the most exciting developments I’ve seen in my medical career. There is now a non-toxic treatment for these problems that literally works miracles in many cases!
[Heparin is NOT a non-dangerous treatment! That is this doctors 'new discovery' described in detail below. Here is data about Heparin:
While you are using this medicine, it is very important that you avoid sports and other activities that may cause you to be injured. Report to your doctor any falls, blows to the body or head, or other injuries, since serious bleeding inside the body may occur without your knowing about it.
Take special care in brushing your teeth and in shaving. Use a soft toothbrush and floss gently. Also, it is best to use an electric shaver rather than a blade. (source) ]
The great question with these illnesses is "what causes them?" I’ve had many patients tell me their fibromyalgia started or flared up after a minor illness or trauma. But that didn’t make sense, as neither of these could possibly cause chronic illness. Or could they?
For years, doctors have wondered why people respond to similar types of trauma in such different ways.
Take for instance Gulf War syndrome. Why did some of the soldiers in the Gulf War come down with this horrible disease, while their unit buddies, who were exposed to the exact same conditions (including vaccines and the war theater in general) never batted an eye? A similar question that’s gone unanswered is why does one child get autism after receiving the same vaccines that had no effect on the kid down the street? Or why do some people who live near an environmental hazard (such as a chemical plant) get cancer, but their neighbors don’t?
Could it be possible that some people could react differently to a minor illness or injury than most people would? The answer is yes! For example, a relative of mine was stricken with scleroderma after a minor auto accident that most people would walk away from without any trouble.
For years, medicine has not understood these observations and would simply classify sufferers of such syndromes as psycho cases. Rarely, if ever, did blood tests show any pathology other than perhaps non-specific markers of inflammation or, in the case of autoimmune disease, antibodies seemingly directed against the body.
But I just can’t accept the idea of autoimmune disease, as I don’t believe God would create a body that directs its immune system to destroy itself.
[Karl Note: So far, not too bad. It is very true that different people react differently to the same bacteria or health problem. But, he then goes looking down the chemical trail, completely devoted to the man-is-mud theory of Dr. Wundt, and the godless promotion of that idea some houndred years ago by John D. Rockefeller.]
The good news is that new findings are now proving my suspicions correct. And, more importantly, these same findings are showing an underlying theme in most chronic disease cases, which opens exciting new possibilities for treatment!
[Karl Note: I, of course, am not a doctor, a mere philosopher and researcher. I HAVE solved this problem, but doctors won't read my stuff! Perhaps you will? Take a look at the famous poem, The Blind Men and the Elephant, below. Click here for a full page text. This doctor is not mentally capable of seeing a non-material causation!]
The
path to solving this puzzle began when a doctor observed that women with
infertility problems uniformly had a blood clotting pattern that’s nearly
identical to a condition called diffuse intravascular coagulation (clotting
inside the blood vessels for no apparent reason).
Blood clotting is a very complex, highly guarded and regulated system within all animals with a circulatory system. Much like a teeter-totter, too much activity can lead to unnecessary and dangerous clots, while too little activity can leave you prone to excessive bleeding. Some 40 percent of all proteins in human blood are intertwined with this complex system. There are pathways that lead to clotting (to prevent bleeding) and equivalent pathways to control it and dissolve unnecessary clots (preventing thrombosis). Medical science recognizes both of these extremes as major problems requiring medical intervention.
The real news, though, is coming from studies which are now demonstrating that there’s an intermediate zone where the patient does not have an overt clot, but the blood is still clotting enough to cause problems, including chronic disease!
The jump from overactive clotting to chronic illness is rather complex (which is why researchers have missed it for so long), but there is a direct connection, as you will soon see.
In the normal process of inflammation, chemicals are released to activate the immune system to a properly controlled fight. The coagulation (clotting) system also gets activated as part of this process. The normal person will recover from the illness or physical trauma and the coagulation system will return to normal. However, a significant number of people from European descent are carrying a genetic trait that causes the clotting system to remain active and not tone down.
[Karl Note: This doctor, like most, has fallen into the trap set by Dr. Wundt, and financed by John D. Rockefeller. That trap is that man is made from mud -- from a sea of chemicals. Since man arose from chemicals, chemicals can cure him. That concept, of course, rules out God. When this doctor uses the word "God" he uses it in a way that shows he has no clue there either.]
The clotting system is designed to burst forth with fibrin, a protein that crosslinks with other fibrin molecules to form a clot which stems the breech. A clot would look something like a cotton ball, with all the single strands of the cotton condensing into the ball (clot). This is the body’s normal response to an injury. When the injury is repaired, other proteins dissolve away the clot.
The problem arises when all of these single strands of fibrin do not come together into a clot, but remain as freestanding single soluble fibrin monomers (SFM). This would be analogous to the individual wisps or strands of the cotton ball never clumping together. Even though these fibrin molecules do not come together to form a clot, they are still very sticky and begin to stick to and coat the inner lining of the blood vessels. Coating the smaller blood vessels in this fashion effectively sludges them up, significantly limiting oxygen and nutrient exchange across the capillaries.

[Karl Note: Here is a much more valid explanation of what is happening:
John Scientist notices that on every person he sees who has had a stroke, the homocysteine level in the blood is high. He then looks at a group of people who have not had strokes. Their homocysteine levels are NOT high.
He DECIDES that high homocysteine levels CAUSE heart disease. It does not occur to him that heart disease, or strokes, could cause high homocysteine levels.
He doesn't worry about the "function" of homocysteine. He is content with identifying the substance and giving it a label.
Various people have puzzled about the inner conflicts in this data, but they usually smooth over the cracks and pretend there are none. Occasionally, you'll see a glimpse of truth:
Atherosclerotic plaques deposit in response to injury. This major finding led to the 1985 Brown-Goldstein Nobel prize in medicine. The confusion in the media is cause and effect. The fallacy is that cholesterol causes heart disease, but plaque build-ups are the effect of heart disease. G. C. Willis, MD, made the crucial observation in the early 1950s. A Canadian doctor, he noticed that atherosclerotic plaques in his patients kept forming in the same places. Usually near the heart where the blood vessels are stretched and bent. Willis was the first to implicate high blood pressures and the mechanical stress caused by the heart beat. The Pauling and Rath theory relies on this observation that plaque does not form randomly throughout the blood stream. (Note: In a heart bypass, veins from the leg are used which are without plaque.) Accordingly, it is unlikely that the primary cause of the lesions leading to heart disease are "poisons" circulating in the blood. (source)
The above statement starts to reveal some truth, but then stumbles into more false data!
Then, things get complicated. This John Scientist also notices that people with high levels of homocysteine have high cholesterol. He "knows" that high cholesterol causes heart disease. So, he thinks he has found a cause for high cholesterol in the high level of homocysteine. This is Nobel Prize stuff.
He still doesn't know the function of either cholesterol or homocysteine relative to heart disease, but he is certain that if you could get a drug to lower homocysteine, you would lower cholesterol, and then reduce heart disease.
This goes along for a few more tens of millions of research dollars. Then, someone "proves" that high levels of cholesterol do NOT cause heart disease. So, he is left with only part of a theory. He can "back and fill" with some new terminology, and "discover" that high levels of homocysteine cause heart disease directly.
Then, some other "association" comes along.
What is happening here?
What is happening is that medical researchers very seldom can tell the difference between a cause and effect. They are good at identifying the chemical nature of some substance, and giving it a label. They are good at inventing cause and effect relationships, without any necessity of establishing the function of these substances, or the truth about cause or effect.
An actual Nobel Prize was awarded in 1985, covering the "fact" that cholesterol causes heart disease:
Cholesterol is of vital importance but may also be deleterious, and far more so than by causing gallstones. Since the middle of the nineteenth century it has been known that in atherosclerosis, cholesterol, or rather cholesterol esters, accumulate in high concentrations in the lesioned areas of the blood vessels, and since the late 1930s a specific inheritable disease, familial hypercholesterolemia, has been recognized, with greatly increased concentrations of cholesterol in the blood, and severe alterations in the normal structure of blood vessels. (source)
The proof that cholesterol does NOT cause heart disease is well proven, but not likely to get noticed by the Nobel Prize Committee. Click here for that story.
Here is a explanation of the problem to any researcher of determining cause and effect based on association:
Thus, the risk of having a heart attack is greater than normal for people with high LDL-cholesterol, but so is the risk for fat, sedentary, smoking, hypertensive and mentally stressed individuals. And since such individuals usually have elevated levels of LDL-cholesterol, it is, of course impossible to know whether the increased risk is due to the previously mentioned risk factors (or to risk factors we do not yet know) or to the high LDL-cholesterol. A calculation of the risk of high LDL-cholesterol that ignores other risk factors is called a univariate analysis and is, of course, meaningless.
To prove that high LDL-cholesterol is an independent risk factor, we should ask if fat, sedentary, smoking, hypertensive and mentally stressed individuals with a high LDL-cholesterol level are at greater risk for coronary disease than fat, sedentary, smoking, hypertensive and mentally stressed individuals with low or normal LDL cholesterol.
Using complicated statistical formulas, it is possible to do such comparisons in a population of individuals with varying degrees of the risk factors and varying levels of LDL-cholesterol, a so-called multivariate analysis. If a multivariate analysis of the prognostic value of LDL cholesterol also takes body weight into consideration, it is said to be ”adjusted for body weight”.
A major problem with such calculations is that we know a great number of risk factors because the more risk factors that are adjusted for, the less reliable the result will be. Another problem is that the data generated by these and other complicated statistical methods are almost impossible for most readers, including most physicians, to comprehend.
For many years researchers in this area have not presented primary data, simple means, or simple correlations. Instead, their papers have been salted with meaningless ratios, relative risks, p-values, not to mention obscure concepts such as the standardized logistic regression coefficient, or the pooled hazard rate ratio.
Instead of being an aid to science, statistics are used to impress the reader and cover the fact that the scientific findings are trivial and without practical importance. Nevertheless, let us have a look at some of the studies. (source)
Karl Note: The original article from which this excerpt is taken then goes on to demolish the studies that showed, falsely, that high levels of cholesterol CAUSES heart disease.
This doctor is doing the same type of fallacious logic.]
After last month’s issue, you already know how important oxygen is to healing and how grave it is to limit it. Imagine piling layer upon layer of dead weight on the critical lining of the capillaries. The effect on the underlying tissues and the body as a whole is devastating.
The next questions to consider are: (1) What activates this process and keeps it activated? And (2) why are the disorders so prevalent? David Berg, MS, director of Hemex Laboratories, explains it like this:
"Imagine yourself in Europe several hundred years ago with swords, spears, and arrows a-flying. If you were to get hit with one, you would have a much better chance of survival if your clotting pathway was highly active and stopped the bleeding very quickly. Your genes would survive to be passed down. If you didn’t have the gene, you would be more likely to bleed to death and your genes wouldn’t be passed down. Thus, the prevalence of the genetic predisposition to highly or easily activated coagulation. In those days, this genetic trait was an advantage.
"In today’s world, however, our bodies face different threats than spears — unseen microscopic pathogens. In these same individuals, an infection or even a minor injury can activate the clotting system which is where the trouble starts."
Today’s pathogens are evolving rapidly. Somehow, they have figured out that they have a much better chance to survive if they don’t kill the host. These microorganisms don’t like oxygen and have a much better chance if they can go undetected by the immune system. In susceptible people, these relatively new infections (i.e., Epstein Barr virus – EBV, mycoplasmas, chlamydias, HHV6 – human herpes 6 virus, and many others) trigger the clotting mechanism. But rather than inciting a clot the way an arrow might, they instead stimulate the production of single strands of fibrin, which coat the blood vessels.
The infection can take up shop, keeping a low enough presence to keep the coagulation pathway active, depriving tissues of needed oxygen, but not enough to trigger an all-out immune response. The deprivation of oxygen can lead to fatigue, aches, pain, headaches, reduced production of hormones (low thyroid, adrenals, etc.), mental aberrations, and more. Sound familiar?
The hardest part for the clinician to date has been to identify a particular abnormality in these patients, or to identify an infection. These low-grade infections don’t operate like classical infections such as strep or staph.
They don’t activate the immune system enough to even see abnormal immunity in routine testing. The organisms are hidden away in tissues and cannot be cultured in the blood.
Recently, the development of antibody testing and PCR (polymerase chain reaction) in which the DNA of the infecting agent can be greatly magnified and seen has made it easier to find these infections when the physician is astute enough to look.
At last we have an explanation of why some people go on and get a chronic infection and symptoms, while others recover promptly and heal completely.
Action to Take
In order to treat any of the various chronic ailments, you first have to root out the offending organisms and offer starving cells the oxygen they crave. Some doctors have tried to use the drug coumadin (warfarin), but it doesn’t solve the problem. The underlying activation still progresses.
On the other hand, heparin (which unfortunately at this moment is available and functional only by injection) does offer dramatic relief. Administered by a simple subcutaneous injection, much like insulin, the results in patients can be nothing short of dramatic.
At a recent medical conference, Dr. Ryser, who regularly uses heparin therapy, reported the incredible results she’s seen in some very difficult-to-treat cases like fibromyalgia and chronic fatigue syndrome. Dr. Ryser said she’s seeing a fantastic 80 percent cure rate.
Of course, heparin is not the only answer. Dr. Ryser is employing a wide range of nutritional supplements to activate the immune system, and I also use regular oxygen therapy.
Susan, the woman I mentioned at the beginning of this letter, finally found a doctor who understood fibromyalgia and was put on heparin and nutritional support.
Within weeks she was able to return to the productive world, completely free of any debilitating problems.
One of my first cases was a woman who lives in a remote area of Alaska. Her soluble fibrin monomers and other clotting factors were quite elevated. Within two days after starting heparin, she excitedly called to tell me the fog over her brain had lifted, her energy was dramatically restored, and while the pain was still present, she could now tolerate it and there were periodic breaks from it.
Of course, because of the variability of the clotting disorders, some patients may respond this quickly, while others may take weeks or even months to unlayer years of fibrin deposition. A health professional I’ve treated for years has intractable high blood pressure (it’s genetic in her case). She’s seen virtually no response to any non-pharmacological intervention and an extremely poor response to prescription medications. When I started her on the heparin, I reduced her prescription medication to one-third the amount she was taking. Within two weeks, her blood pressure had fallen to normal for the first time in memory. Her pressure was 160/110 at the outset.
Another patient of mine is from Australia and travels to Alaska every one to two years for oxidation and homeopathic treatment for an intractable infection, which causes him severe joint pains, fatigue, and asthma.
I recently visited his home country and started him on low dose heparin. The next day his joint pains were dramatically reduced and his lungs improved considerably.
If you suffer from any chronic ailment, low-dose heparin may be just what you need. Hemex Laboratories of Phoenix, Arizona provides excellent state-of-the-art measurements of several key clotting factors that are not measured by any conventional test or lab. They also offer a genetic panel that can probe more deeply into the individual’s problem, which helps determine whether treatment should be with heparin, enzymes and nutrients, or all three. Anybody with long-term unresolved or unexplained problems is a candidate for this evaluation.
More information on the lab and treatment plans can be obtained by visiting www.hemex.com .
Thus far, I’ve tested over 20 patients in just a few months and all of them had an activated clotting mechanism.
So I highly recommend you see a doctor who is familiar with coagulation therapy and have the test per-formed (contact IOMA at P.O. Box 891954, Oklahoma City, OK 73189, 405-478-4266. Send a written request and $5.00 for a list of doctors). It just may be the first step down your road to recovery.
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Heparin ( HEP-a-rin) is an anticoagulant. It is used to decrease the clotting ability of the blood and help prevent harmful clots from forming in the blood vessels. This medicine is sometimes called a blood thinner, although it does not actually thin the blood. Heparin will not dissolve blood clots that have already formed, but it may prevent the clots from becoming larger and causing more serious problems.
Heparin is often used as a treatment for certain blood vessel, heart, and lung conditions. Heparin is also used to prevent blood clotting during open-heart surgery, bypass surgery, and dialysis. It is also used in low doses to prevent the formation of blood clots in certain patients, especially those who must have certain types of surgery or who must remain in bed for a long time.
Heparin is available only with your doctor's prescription, in the following dosage form:
In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For heparin, the following should be considered:
Allergies—Tell your doctor if you have ever had any unusual or allergic reaction to heparin, to beef, or to pork. Also tell your health care professional if you are allergic to any other substances, such as foods, preservatives, or dyes.
Pregnancy—Heparin has not been shown to cause birth defects or bleeding problems in the baby. However, use during the last 3 months of pregnancy or during the month following the baby's delivery may cause bleeding problems in the mother.
Breast-feeding—Heparin does not pass into the breast milk. However, heparin can rarely cause bone problems in the nursing mother. This effect has been reported to occur when heparin is used for 2 weeks or more. Be sure to discuss this with your doctor.
Children—Heparin has been tested in children and, in effective doses, has not been shown to cause different side effects or problems than it does in adults.
Older adults—Bleeding problems may be more likely to occur in elderly patients, especially women, who are usually more sensitive than younger adults to the effects of heparin.
Other medicines—Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking heparin, it is especially important that your health care professional know if you are taking any of the following:
Other medical problems—The presence of other medical problems may affect the use of heparin. Make sure you tell your doctor if you have any other medical problems, especially:
Also, tell your doctor if you have received heparin before and had a reaction to it called thrombocytopenia, or if new blood clots formed while you were receiving the medicine.
In addition, it is important that you tell your doctor if you have recently had any of the following conditions or medical procedures:
If you are using these injections at home, make sure your doctor has explained exactly how this medicine is to be given
To obtain the best results without causing serious bleeding, use this medicine exactly as directed by your doctor. Be certain that you are using the right amount of heparin, and that you use it according to schedule . Be especially careful that you do not use more of it, do not use it more often, and do not use it for a longer time than your doctor ordered.
Your doctor should check your progress at regular visits
The dose of heparin will be different for different patients and must be determined by your doctor. The dose you receive will be based on the type of heparin you receive, the condition for which you are receiving heparin, and your body weight.
If you miss a dose of this medicine, use it as soon as possible. However, if it is almost time for your next dose, do not use the missed dose at all and do not double the next one. Doubling the dose may cause bleeding. Instead, go back to your regular dosing schedule. It is best to keep a record of each dose as you use it to avoid mistakes. Be sure to give your doctor a record of any doses you miss. If you have any questions about this, check with your doctor.
To store this medicine:
Do not take aspirin while using this medicine
Tell all medical doctors and dentists you visit that you are using this medicine
It is recommended that you carry identification stating that you are using heparin. If you have any questions about what kind of identification to carry, check with your health care professional.
While you are using this medicine, it is very important that you avoid sports and other activities that may cause you to be injured. Report to your doctor any falls, blows to the body or head, or other injuries, since serious bleeding inside the body may occur without your knowing about it.
Take special care in brushing your teeth
and in shaving. Use a soft toothbrush and floss gently. Also, it is best to use
an electric shaver rather than a blade.
Since many things can affect the way your body reacts to this medicine, you should always watch for signs of unusual bleeding. Unusual bleeding may mean that your body is getting more heparin than it needs.
Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
Check with your doctor immediately if any of the following signs and symptoms of bleeding inside the body occur:
Abdominal or stomach pain or swelling; back pain or backaches; blood in urine; bloody or black, tarry stools; constipation ; coughing up blood; dizziness ; headaches (severe or continuing); joint pain, stiffness, or swelling; vomiting of blood or material that looks like coffee grounds
Also, check with your doctor immediately if any of the following side effects occur, since they may mean that you are having a serious allergic reaction to the medicine:
Changes in the skin color of the face; fast or irregular breathing; puffiness or swelling of the eyelids or around the eyes; shortness of breath, troubled breathing, tightness in chest, and/or wheezing; skin rash, hives, and/or itching
Also, check with your doctor as soon as possible if any of the following occur:
Bleeding from gums when brushing teeth; heavy bleeding or oozing from cuts or wounds; unexplained bruising or purplish areas on skin; unexplained nosebleeds ; unusually heavy or unexpected menstrual bleeding
Other side effects that may need medical attention may occur while you are using this medicine. Check with your doctor as soon as possible if any of the following side effects occur:
Less common or rare
Back or rib pain (with long-term use only); change in skin color, especially near the place of injection or in the fingers, toes, arms, or legs; chest pain; chills and/or fever; collection of blood under skin (blood blister) at place of injection; decrease in height (with long-term use only); frequent or persistent erection; irritation, pain, redness, or ulcers at place of injection; itching and burning feeling, especially on the bottom of the feet; nausea and/or vomiting; numbness or tingling in hands or feet; pain, coldness, or blue color of skin of arms or legs; peeling of skin; runny nose; tearing of eyes; unusual hair loss (with long-term use only)
Other side effects not listed above may also occur in some patients. If you notice any other effects, check with your doctor.
Revised: 08/23/1994
Copyright© 2000
Micromedex, Inc. All rights reserved. USP DI® and Advice for the Patient® are
registered trademarks of USP used under license to Micromedex, Inc. Information
is for End User's use only and may not be sold, redistributed or otherwise used
for commercial purposes.
Helping to solve blood curdling mysteries.
Chronic Fatigue / Fibromyalgia
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HEMEX Laboratories is an accredited laboratory specializing in the evaluation of disorders in hemostasis, thrombosis, and special hematology. HEMEX offers more than just reports. We offer a full range of clinical testing, interpretation, pathologist review, and consultation to assist clinicians in the diagnosis and treatment of a wide range of coagulopathies and hematological disorders. Over ninety percent of our testing is performed daily providing our clients with quality results in 23 hours. Our research has led to a new approach for the diagnosis, treatment and alleviation of Chronic Fatigue Syndrome/Fibromyalgia, Gulf War Syndrome, and other such disorders. HEMEX Laboratories is committed to ensuring that individual consumers realize the full benefits of the Internet to improve their health and that of their families. To fulfill our commitment, we are dedicated to meeting the following ethical goals as set forth by Hi-Ethics.com.
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