Weblog

Tuesday, April 15, 2008

  • Supperfood, Marine Phytoplankton



    Spirulina, a fresh water plant alae, has helped me a lot and I have used it for a number of years.

    About a month ago I came across a new Supperfood, Marine Phytoplankton. With over 200+ micro algae. It is over 400 times more Powerful than anything else on the planet. The Marine Phytoplankton rebuilds us at a cellular level.

    So far I am experiencing less pain, less dissiness, and feel more energy.

    Marine Phytoplankton gets our immune system working naturally again.

    I feel that I am on my road to recovery and Super Health. Maybe you will feel the same, it is working for other with Chronic Fatique Syndrome, Cancer, etc.

    FrequenSea is the name of what I amusing, which has the Marine Phytoplanton in it, there is a video to explain more about FreqeunSea and Marine Phytoplankton.I have a few more video's to share with you to soon.

    Ok, Yea, here are a three videos for you to learn more about FreqeunSea and Marine Phytoplankton.

    Superfood, Marine Phytoplankton

    The Carrie Host Story - Hope with a rare Cancer

    Ulcerative Colitis - Road back to health - Frequensea

    Many Blessing's My Friend's !!!******


     

Wednesday, June 13, 2007

Tuesday, March 02, 2004

  • I find this useful information, so am passing it on to you.

    [Moderator's Note: Please respond directly to
    Rich Van Konynenburg, Ph.D. <Richvank@AOL.COM>]


    From Rich Van Konynenburg:

    I've updated my general outline for dealing with cases of CFS, and I
    would like to receive comments on it.


    DRAFT FOR COMMENT

    March 1, 2004



    SUGGESTED GENERAL OUTLINE FOR DEALING WITH CASES OF
    CHRONIC FATIGUE SYNDROME

    by

    Richard A. Van Konynenburg, Ph.D.

    (richvank@aol.com)


    Disclaimers

    I am an unlicensed independent researcher with a background in the
    physical sciences and engineering. I have been studying chronic
    fatigue syndrome (CFS) as an avocation for more than seven years.
    Though I am not a clinician or a practitioner and do not accept
    remuneration from clinicians, patients, or vendors of the products
    mentioned herein, I have attached a disclosure statement about
    myself at the end of this document, in keeping with the spirit of
    that part of the California Business and Professions Code that
    pertains to complementary and alternative health care services.

    Where particular products or laboratories are cited in this general
    outline, these citations are intended as possibilities rather than
    specific endorsements. These possibilities are not intended to rule
    out other products or laboratories that may also be available.

    Clinicians or persons with chronic fatigue syndrome who choose to
    follow this general outline do so at their own risk. In particular,
    as an unlicensed researcher I am not authorized to prescribe
    pharmaceuticals. Where these are mentioned, they are intended only
    as possibilities for consideration by licensed health care
    practitioners, who remain responsible for their prescription.

    I am hopeful that this general outline will be of help to those
    suffering from chronic fatigue syndrome as well as those who treat
    them.

    Basis

    What follows is based on my own hypotheses about CFS and on what I
    have learned from researchers and clinicians who specialize in
    treating these disorders, from papers, books, and conferences, and
    from interactions with people on internet lists, during my years of
    focusing on this disorder. My thoughts on effective methods of
    coping with this disorder continue to change as I learn more, but
    this is a snapshot of my present views. While I cannot guarantee
    that they will bring about a cure of CFS, I am confident that they
    can improve the quality of life for many PWCs (persons with chronic
    fatigue syndrome).

    Audience

    This paper is written both for clinicians who treat CFS and for PWCs
    themselves. Many of the actions discussed herein can only be
    performed by PWCs on their own behalf. Other aspects can only be
    performed by licensed health care professionals. It is my hope that
    this general outline will foster increased cooperation between PWCs
    and clinicians to improve the methods for dealing with CFS

    Application

    This general outline is intended to apply to PWCs who have been
    diagnosed as having CFS according to "Myalgic
    Encephalomyelitis/Chronic Fatigue Syndrome: Clinical Working Case
    Definition, Diagnostic and Treatment Protocols," by Carruthers, et
    al. (Journal of Chronic Fatigue Syndrome, vol. 11, no. 1 (2003)).
    These diagnostic criteria were developed by a consensus committee
    under the auspices of Health Canada.

    This general outline is also appropriate for PWCs diagnosed under
    the older Fukuda et al. international research case definition
    developed under the auspices of the U.S. Centers for Disease Control
    and Prevention in Atlanta, GA.

    It is particularly important to make efforts to rule out Lyme
    disease in people who have CFS-like symptoms. This has been very
    difficult to do, and many have suffered from Lyme disease for years
    while carrying a diagnosis of CFS. The NIH has recently announced a
    new test for Lyme disease. If it turns out to be reliable, it will
    be a major contribution.

    Multifaceted Nature of Approach

    To be most beneficial, a treatment program for CFS must be
    multifaceted, combining several types of interventions. The reasons
    for this are that CFS affects the human organism at a very
    fundamental level, and it has an exceedingly complex pathogenesis,
    composed of many steps, interactions, and vicious circles, many of
    which still remain to be elucidated. The longer a PWC has been ill,
    the more involved this pathogenesis becomes. A single treatment
    intervention will not be sufficient to break through this web.
    Figuratively speaking, to bring a PWC back out of the CFS pit, she
    or he must be lifted at several places, some of them simultaneously,
    others in appropriate chronological order. Most of the clinicians
    who treat many PWCs (including Dr. Paul Cheney and Dr. Jacob
    Teitelbaum) have found that a multifaceted treatment approach is the
    most effective.

    Subsets and Tailoring to Individual PWCs

    The PWC population as currently defined by the above diagnostic
    criteria is heterogeneous, composed of many subsets. There are few
    serious CFS researchers who doubt this, and many are now emphasizing
    the importance of separating the subsets in order to make further
    progress in understanding the causes of CFS. Consequently, a
    single, uniform treatment protocol is not appropriate and will not
    be effective for all PWCs. In the general outline described here,
    there are many parts, and I have attempted to point out criteria for
    inclusion of the various parts when tailoring to an individual PWC.

    Chronological Order of Interventions

    Some of the aspects of this general outline are best carried out in
    a certain chronological order. This order is based on the
    interactions and vicious circles that are characteristic of the
    current pathophysiology of the PWC rather than on the order in which
    the various body systems were affected during the pathogenesis.
    Where the order of interventions is important, I have specified it,
    to the best of my current understanding.

    Description of the Parts of the General Outline

    1. Stress Relief

    Many PWCs were overloaded by various types of long-term stressors
    prior to the onset of their symptoms, and some continue to be so.
    There is considerable published research supporting the observation
    of stressors in the etiology of CFS. In an initially healthy human,
    the long-term stress that results from these stressors causes the
    secretion of adrenaline and cortisol by the adrenals for extended
    periods, and these lead to suppression of cell-mediated immunity and
    depletion of glutathione, which in turn can produce a range of
    deleterious effects, leading to CFS in genetically susceptible
    individuals. Unless the load of stress is lifted or at least
    greatly reduced, it is probably not possible to achieve health, so
    this aspect should be dealt with early.

    Even though it may be extremely difficult to do, it's important for
    PWCs to do whatever they can do to relieve their load of various
    kinds of stressors, including physical, chemical, biological,
    mental, and emotional stressors. This includes changing their actual
    life circumstances as well as changing how they respond to these
    circumstances. They may have to make some hard decisions and stick
    to them. If they have not already dropped out of their employment,
    they may have to. If there are interpersonal interactions in their
    lives that cause them excessive stress, they will either need to
    make peace with the people involved or minimize their interactions
    with them. If their living environments are exposing them to
    significant amounts of chemical toxins or irritants, it will be
    critical for them to eliminate these substances or to move to other
    dwellings. If they are overdoing physical exercise or exertion,
    they will need to moderate it. If they are repeatedly being exposed
    to infections, they will need to isolate themselves from the sources
    of these infections.

    Pacing is an important habit for PWCs to develop. Before becoming
    ill, many PWCs were achievement-oriented, action-prone, "Type A,"
    hard driving people. Recovery from CFS will demand a fundamental
    change in this approach to life. Instead of attempting always
    to "do one's best," a PWC may need to come to terms with doing
    something that is quite good enough. Tomorrow is another day.
    Balance is called for.
    Instead of ignoring signals from the body that rest is needed and
    forging full steam ahead, a PWC should develop the habit of heeding
    these signals and lightening the load. This advice may seem like
    heresy to a person whose life has been oriented since childhood
    toward maximum achievement or perfection, but I believe it's the
    correct advice when it comes to promoting recovery from CFS.

    Once PWCs have made the changes necessary to reduce their stress to
    a manageable level, they must seek to improve the ways in which they
    cope with their remaining stress: they should consider activities
    such as listening to music, meditating, praying, practicing yoga,
    watching comedy videos or radio programs, developing their sense of
    humor, and enjoying nature. If they have deep-seated animosities
    because of past wrongs done to them, they should work on developing
    the ability to forgive. Different things work for different people.

    Of course, it is much easier to talk about reducing stress and
    coping with it than to actually do these things. The degree to
    which PWCs can reduce the stress in their lives depends on what
    their financial picture is, whether or not they have a supportive
    social structure, and other factors. But the more they can rid
    themselves of stress and/or learn to cope with it more effectively,
    the better will be their chance for recovery.

    2. Exercise

    There is a continuing controversy over the benefit of exercise in
    CFS. My view of this is that too much exercise, particularly of
    aerobic types, is damaging to a PWC, but appropriate amounts of the
    right kinds of exercise can be beneficial.

    I believe that damage to the skeletal muscle cells occurs as a
    result of the increased production of oxidizing free radicals during
    aerobic exercise, in the presence of an ongoing condition of
    oxidative stress in these cells. There are now several papers in
    the literature reporting on elevated measurements of markers of
    oxidative stress in CFS. It is well-established that oxidizing free
    radicals are produced in the normal course of metabolism, and that a
    higher rate of metabolism will result in a higher rate of production
    of oxidizing free radicals. I believe that this accounts for the
    observed "post-exertional malaise" that may extend for days after a
    PWC gets too much exercise.

    Movement, stretching, and resistance exercise are important for the
    health of the joints, the bones, the lymph system, the circulatory
    system, the vestibular (balance) system, the tendons and muscles and
    the digestive system. The joints require physical movement in order
    to bring nutrients to the cartilage via the synovial fluid. The
    maintenance of strong bones requires mechanical stress in the
    bones. The lymph system requires the action of skeletal muscles to
    move lymph from the periphery of the body into the thoracic duct and
    thence into the circulatory system. The circulatory system requires
    muscle action to assist in returning blood to the heart, as well as
    in preserving the tone of the heart muscle and the condition of the
    overall circulatory system. Bouncing type exercise (such as on a
    small trampoline or a chair suspended with springs) has been found
    helpful for the vestibular system. The muscles and tendons require
    exercise to stay in condition, and exercise can also help to relieve
    muscle pain. The digestive system benefits from exercise in
    maintaining proper motility.

    PWCs should get regular exercise, but should not overdo it. They
    should approach exercise cautiously, doing less than they think they
    can, and waiting until the next day or two to decide whether they
    are able to tolerate it at the level achieved. Increases in exercise
    parameters should be entered upon cautiously. PWCs should avoid
    aerobic exercise, but carry out stretching, movement, and short-term
    (non-aerobic) resistance exercise. For people who have
    fibromyalgia only, without symptoms characteristic of CFS, even
    aerobic exercise can be helpful.

    3. Relief of Pain

    Muscle pain, and to a lesser extent joint pain, are major symptoms
    for many PWCs. Most of this pain does not appear to be associated
    with observable tissue damage, but rather seems to originate in
    malfunction of the sensory parts or pain signal processing parts of
    the nervous system. Since severe pain can interfere with the
    ability to obtain restorative sleep and can also stimulate the
    hypothalamus-pituitary-adrenal axis, it should be dealt with before
    treating sleep problems or the neuroendocrine system. Some pain
    relief can often be obtained from appropriate exercise, such as
    stretching and relaxation, as mentioned above. Pain relief can also
    often be obtained from massage, acupuncture, chiropractic, physical
    therapy, or local or general heating. Far-infrared heating, in
    particular, appears to offer advantages. Pharmaceutical pain
    relievers are often used by clinicians. Their benefits must of
    course be weighed against their side effects, and in the case of the
    more potent ones, their habituation tendencies.

    4. Sleep

    Sufficient deep, restorative sleep is very important for several
    reasons. Human growth hormone is secreted by the pituitary gland
    during the deepest stages of sleep (Stages 3 and 4). This hormone is
    necessary to carry out repairs while we sleep. In addition, memories
    of daily events are fixed in our brains during sleep, and poor sleep
    quality can lead to deficits in short-term memory. Biochemical
    energy supplies are restored in the brain during sleep. There are
    probably many more benefits of restorative sleep that are not yet
    understood.

    PWCs should do what they need to do to get the amount of restorative
    sleep nightly that is sufficient for them to feel rested when they
    awaken. Seven to eight hours per night is appropriate for most
    people. This should start with avoiding foods (such as caffeine) and
    activities in the period before bedtime that tend to keep people
    awake. It's important to have a regular bedtime and a quiet, dark
    place to sleep
    with a comfortable temperature and a reasonably comfortable
    mattress. If this doesn't bring restorative sleep, then PWCs should
    look into the possibility that they might have sleep apnea, as
    follows: If he or she has a sleeping partner, the partner can be
    asked whether he or she has noticed that the PWC stops breathing for
    periods of time while sleeping, a sign of sleep apnea. If the PWC
    frequently awakens with a gasp or a snort, this is another sign of
    sleep apnea. Snoring or a neck size larger than 17 inches are other
    risk factors for sleep apnea. If suggestions of sleep apnea are
    present, a clinician can order a sleep study to determine whether a
    PWC has this condition for sure, and if so, a CPAP machine may be
    helpful. If these measures don't bring restorative sleep, then the
    orthomolecular substances should be tried first, such as a magnesium
    supplement or melatonin at bedtime. If they don't correct the
    problem, an herbal mixture including valerian, passion flower, kava
    kava, and others (such as from www.immunesupport.com) should be
    tried. If that doesn't work, the clinician should consider
    prescribing zolpidem (Ambien). Antihistamines such as Benedryl
    (diphenhydramine) may promote sleep, but may also interfere with
    deep-stage sleep.

    5. Air

    Many PWCs suffer from respiratory allergies, multiple chemical
    sensitivities, and/or deficits in the operation of their
    detoxication system. Therefore, it's important for them to be able
    to breathe air that is free of toxins, allergens, and substances to
    which a PWC may have a chemical sensitivity.

    The home heating system should be checked for leakage of carbon
    monoxide into the living space. Furnishings and building materials
    that outgas volatile substances such as formaldehyde or emit mold
    spores should be eliminated. A high efficiency particulate air
    (HEPA) filter should be installed to remove pollens and dusts, if
    they cause allergic reactions.

    6. Water

    It is important to drink sufficient water for proper hydration of
    the body and for proper operation of the bowels. Many PWCs have a
    higher than normal requirement for water, because they suffer from
    central diabetes insipidus (not the same as the more common diabetes
    mellitus). Central diabetes insipidus results from insufficient
    secretion of antidiuretic hormone by the hypothalamus and pituitary
    gland, and this causes the kidneys to pass too much water into the
    urine. The result is constant thirst and low blood plasma volume.
    The latter exacerbates problems with orthostatic intolerance
    (inability to stand for a significant length of time because of poor
    blood supply to the brain).

    Several of the minerals found in natural waters are among those
    essential to the body, and many PWCs are deficient in some of them,
    particularly magnesium and calcium.

    As noted above, the detoxication system is not operating properly in
    many PWCs (primarily because of glutathione depletion). Therefore,
    minimizing the content of toxins in ingested water is important.

    A PWC should obtain a supply of clean water to drink. It's best if
    it does not contain chloride, fluoride, or significant amounts of
    heavy metals, organic toxins, or bacteria, but the minerals needed
    by the body, such as calcium and magnesium, should not be removed.
    Distilled water or water that has been through reverse osmosis are
    not the best choices, because they do not contain these minerals. A
    home tap water filter that includes a charcoal filter to remove
    heavy metals and organic toxins is a good investment.

    7. Orthostatic Intolerance

    Many PWCs suffer from orthostatic intolerance, manifested as
    orthostatic hypotension (sometimes diagnosed as NMH or neurally
    mediated hypotension) or postural orthostatic tachycardia (POTS), or
    both. These can involve a low blood plasma volume or pooling of
    blood in the lower body when standing, or both.

    The blood plasma volume can be increased to some degree by drinking
    more water, together with added salt. It's important to make sure
    that enough potassium is taken in to maintain the sodium/potassium
    balance in the body. Fresh, non-starchy vegetables are good sources
    of potassium without abundant sugars.

    Blood pooling can be counteracted by the use of support hose. The
    tightness should be selected to prevent blood pooling, but should
    allow sufficient blood circulation in the legs and feet.

    Taking supplemental tyrosine at a dosage of up to 1,500 mg per day
    is another thing to consider to counteract blood pooling, because
    tyrosine is the substrate for making norepinephrine, the
    neurotransmitter used by the sympathetic nervous system to contract
    the muscles around the veins in the lower body. There is evidence
    of low tyrosine in some PWCs and of a deficit in norepinephrine
    production in some with othostatic intolerance.

    Fludrocortisone has been prescribed by some clinicians as a
    treatment for orthostatic intolerance in PWCs, but its efficacy is
    not clear. Midodrine has also received some testing, and has been
    helpful for some with orthostatic hypotension. It is an alpha-1
    adrenoceptor agonist, and thus acts in place of norepinephrine to
    constrict blood vessels. Clinicians should be alert, however, to
    possible excessive elevation of supine blood pressure by this agent.

    8. Diet and Nutrition

    The normal, healthy human body has requirements for about 40
    essential nutrients to support its biochemistry and sufficient
    calories to provide the needed energy. Under normal conditions the
    gastrointestinal system is able to obtain enough of these nutrients
    from the diet to supply the needs of the cells to a significant
    degree (though perhaps not an optimum degree), and the cells are
    able to metabolize the nutrients from food to maintain normal
    function and at least a nominal condition of health.

    In the case of PWCs, there are two categories of problems in this
    area. First, while the gastrointestinal system functions well in
    some PWCs, in many others it does not. Second, in many PWCs the
    skeletal muscle cells in particular are not able to carry out
    oxidative metabolism of absorbed fuels in a normal manner or at
    normal rates. (This appears to be a result of partial blockades in
    the Krebs cycle produced by a rise in peroxynitrite secondary to
    glutathione depletion. Prof. Martin Pall has theorized and
    published extensively about peroxynitrite in CFS.)

    With respect to the first category, it is important for the PWC and
    the clinician to assess the function of the gastrointestinal system
    at the outset to determine the best approach to diet and nutrition
    in the particular case. At one extreme are those whose G.I. systems
    are in such disarray that they are suffering from serious
    malnutrition and deficiencies. These PWCs have difficulty retaining
    sufficient body weight and suffer in many ways from the lack of
    essential nutrients. At the other extreme are those who appear to
    have normal function of their digestive system, and who may have
    great difficulty avoiding constant weight gain. In between are most
    PWCs, who experience varying degrees of malfunction of this system
    and may have some deficiencies in nutrients.

    Problems with the digestive system that are commonly found in PWCs
    include lack of sufficient stomach acid, overgrowth of yeasts and/or
    deleterious bacteria in the intestines, intestinal permeability,
    food allergies, sensitivities or intolerances, and irritable bowel
    syndrome. Celiac disease is occasionally found.

    In cases of serious malfunctions of the gastrointestinal system that
    are producing malabsorption and serious deficiencies of essential
    nutrients, clinicians should consider intravenous nutritional
    interventions, such as the Myers cocktail. This approach bypasses
    the gastrointestinal system and delivers essential nutrients
    directly to the cells via the blood stream. This may be the only
    way to get the boost needed to begin recovery of health.

    If there are problems with the digestive system, it is important to
    deal with them before doing the other things discussed below.
    Specifically, if the digestive system is not producing at least
    daily, well-formed, normal-colored, normal-appearing stools, and the
    PWC is not free of symptoms such as excessive gas (belching or
    flatus), bloating, intestinal cramps, diarrhea, constipation, poor
    stomach motility, gastroesophageal reflux (heartburn), and/or
    multiple food allergies or intolerances, then the gut needs to be
    dealt with before other aspects described below are entered upon.
    There are several reasons for this: a. An efficiently performing gut
    is necessary to absorb nutrients adequately. Without them, the body
    won't be able to obtain what it needs to get well. b. The gut is the
    final pathway for dumping many toxins. If a PWC has had CFS for an
    extended period of time, the body will have large burdens of toxins,
    because the detox system has not been functioning well (largely
    because of the depletion of glutathione), and the toxins will have
    had time to build up. There must be a clear pathway to carry the
    toxins out before one begins to mobilize them, or they will be
    recirculated and may end up in a worse place than where they were
    located initially. For example, more of them may be moved into the
    brain. c. If the PWC has dysbiosis and leaky gut, the resulting
    absorption of antigens directly into the blood stream from the lumen
    of the gut will be placing a heavy load on the immune system, and it
    may not be able to recover unless this load is lifted first.

    Clinicians should first rule out structural causes for
    gastrointestinal symptoms by conventional diagnostic methods. If
    structural abnormalities are not found, a Comprehensive Diagnostic
    Stool Analysis (CDSA) such as is available from www.gsdl.com, should
    be performed. If parasites are suspected, a detailed
    parasitological stool analysis should be performed, such as is
    available from www.parasitetesting.com. The results of these tests
    should be used to augment the bowel treatment program discussed
    below with specific additional remedies as needed.

    I suggest considering the bowel treatment program described by Dr.
    Serafina Corsello in her book "The Ageless Woman," available at
    www.corsello.com. This program includes bowel cleansing, soothing
    and repopulation with probiotics. The detailed ingredients used are
    given in the book, and are all non-prescription items.

    In addition to this bowel treatment program, the most beneficial
    things for promoting normal function of the gut are eating
    sufficient fiber in the diet (fresh fruits and vegetables and whole
    grains), drinking enough water, and getting sufficient (but not
    excessive) exercise.

    Turning now to the second category of problems in diet and nutrition
    in CFS, many PWCs have partial blockades in the Krebs cycles of
    their red, slow-twitch skeletal muscle cells, and these cells are
    thus not able to metabolize carbohydrates completely to carbon
    dioxide and water. When a PWC with such partial blockades continues
    to consume too many carbohydrates, especially those of high glycemic
    index, the results may be surges of insulin, hypoglycemia, and
    conversion of carbohydrates to stored fats, resulting in persistent
    weight gains.

    The metabolism of fats is also limited in many PWCs by the Krebs
    cycle partial blockades, and transfats in particular interfere with
    the proper metabolism of the essential fatty acids and distort the
    structures of cell membranes.

    Proteins are utilized as fuel at higher rates than normal in the
    bodies of many PWCs, because they are broken down into amino acids,
    which are to some degree interconvertible by transamination
    reactions, and some of them are able to compensate for the Krebs
    cycle partial blockades by anaplerosis, and thus to be used
    effectively for fuel.

    As a result of the above, many PWCs find that they feel much better
    on a diet that is relatively high in protein and relatively low in
    carbohydrates and fats, especially low in foods containing
    significant amounts of sugars and white, starchy foods such as
    potatoes, rice, pasta, and bread, and also low in saturated fats and
    transfats. It is important to choose proteins that do not provoke
    an allergic response. Meats are often better tolerated than dairy
    foods or eggs. Vegetables that grow above the ground are good
    choices to supply essential nutrients and fiber.

    With regard to determining the status of the essential nutrients,
    including the vitamins, the minerals, the essential fatty acids, and
    the essential amino acids, the best approach is to perform blood
    tests, such as those offered by www.metametrix.com and
    www.bodybio.com. With results of such testing, it will be possible
    to emphasize supplementation of those nutrients which are
    deficient. If this is not feasible, then I suggest regular
    ingestion of a high-potency general nutritional supplement such as
    Sparx (www.krysalis-sparx.com), two teaspoons of essential fatty
    acids with the ratio of four-to-one linoleic acid to alpha linolenic
    acid, and an undenatured whey protein product such as ImmunoPro Rx
    (for example, from www.immunesupport.com).

    Certain nutrients have been found to be especially helpful to many
    PWCs. These include I.M. or S.C. injections of hydroxocobalamin
    (vitamin B12) at relatively large doses--10,000 micrograms or more
    per injection, two or three times per week. I.M injections of
    magnesium sulfate (100 mg per week) together with taurine (This one
    is painful, but the taurine helps), together with 600 mg magnesium
    as glycinate or malate per day, taken orally. L-carnitine comes in
    here, too, at 1 to 2 grams, three times per day. It's important to
    take lots of antioxidants to counter the condition of oxidative
    stress: 2 grams of vitamin C per day, in divided doses, some
    bioflavonoids, coenzyme Q-10 (100 mg per day, provided it is
    tolerated), and 400 I.U. per day of vitamin E. Alpha lipoic acid
    should be avoided if there is likely a high body burden of methyl
    mercury (such as if the PWC has been eating a lot of large predatory
    fish, such as tuna or swordfish or shark, especially). Otherwise,
    alpha lipoic acid can help to build glutathione, and 100 to 300 mg
    per day can be used. S-adenosylmethionine (SAMe) can be helpful, at
    400 mg, 2X per day, orally (Those with bipolar or manic-depressive
    disorder should avoid taking SAMe, because it can bring on the manic
    phase.)

    There are also some things that should be eliminated from the PWC's
    diet: caffeine, alcohol, MSG, Nutrasweet, food colorings, and other
    artificial food additives.

    More information on diet and nutritional approaches in CFS can be
    found in Chapter 27 of the Handbook of Chronic Fatigue Syndrome
    (Edited by L. Jason et al., Wiley, Hoboken, NJ, 2003), which was
    written by the present author.

    9. Building the Detoxication System and Flushing Out Toxins

    As noted above, toxins build up in the PWC's body over the course of
    the illness, primarily because of glutathione depletion.
    Glutathione is responsible for Phase II detoxication of several
    important categories of toxins, and it also serves as the basis for
    the antioxidant enzyme system, which among other things is necessary
    to deal with oxidizing free radicals produced during Phase I
    detoxication of many toxins.

    Important work has been done on detoxication in recent years by
    Ritchie Shoemaker, M.D., and by Patricia Kane, Ph.D. and her
    coworkers. I suggest that clinicians obtain a copy of The Detoxx
    Book by Foster, Kane and Speight (www.detoxxbook.com) and consider
    the protocols described therein. They include intravenous
    injections of glutathione and phosphatidyl choline as well as oral
    supplementation with appropriate oils and lipids. These measures
    serve to augment the body's supply of glutathione as well as to
    replenish the fatty acids needed by the body and to promote flushing
    of the liver, gall bladder and biliary tract.

    Other methods of helping the body to build glutathione include use
    of oral undenatured whey protein products (such as ImmunePro Rx,
    available from www.immunesupport.com). Use of these in CFS was
    pioneered by Paul Cheney, M.D., Ph.D. This is a very powerful way
    to build glutathione. For those who have allergies to whey protein,
    the use of oral N-acetylcysteine (NAC) and the other amino acids
    making up glutathione (glycine and glutamic acid or glutamine) is
    preferable. Jeff Clark at www.cfsn.com sells such amino acid
    precursors for building glutathione. (Some PWCs react badly to
    anything that contains sulfur, which whey protein and NAC do. If
    this is the case, they should consider taking 250 micrograms of
    molybdenum and 100 mg of vitamin B-6 per day, and
    starting slowly on the NAC or other sulfur-containing supplements.

    It should be noted that it is not always easy to build the
    glutathione levels back up to normal, because there are numerous
    vicious circles that make this difficult, especially if the PWC has
    been ill for an extended period of time.

    When the glutathione begins to build back up, both the detoxication
    system and the immune system will start to come alive, and they will
    start moving toxins into the blood stream. This may produce an
    exacerbation of symptoms known as the Herxheimer reaction, and this
    may require a reduction in dosage. Having generous amounts of
    indigestible fiber in the diet at this time is helpful to bind
    toxins in the gut and carry them out in the stools.

    10. Correcting Low Metabolic Rate and Furthering the Detoxification

    Many PWCs have a lower than normal metabolic rate in their skeletal
    muscles as a result of the partial blockades in the Krebs cycles
    there. The results are that they exhibit a low armpit temperature
    and they feel cold much of the time, even if they have normal
    thyroid function (which many don't). In addition, many PWCs have
    accumulated various toxins in their bodies, as noted above. Use of
    far infrared (FIR) heating serves to simultaneously raise the
    metabolic rate and sweat out toxins. Sherry Rogers has been a
    proponent of FIR for detox. It's important to use FIR heating,
    which penetrates into the tissues, and not other types of heating,
    such as standard near-infrared bulbs, dry or wet ordinary saunas, or
    hot baths or showers, because these methods deposit heat primarily
    in the skin. Heating the skin results in dilating the arterioles
    that supply blood to the skin, and in many PWCs this will provoke
    low blood pressure or tachycardia because of lack of sufficient
    blood flow to the brain.

    PWCs who feel cold much of the time, or who have armpit temperatures
    upon awakening that are significantly below normal, should consider
    FIR heating. In the order of cost, beginning with the lowest cost,
    this is available in the forms of individual FIR lamps, FIR heaters
    that stand on the floor, FIR sauna tunnels, and upright FIR saunas.
    One approach (pioneered by Jim Clements) is to get two FIR heaters
    (so you can sit between them) and use them for about 15 or 20
    minutes a couple of times per week. Unless a tunnel or full sauna
    is used, it may be necessary to warm the room first (a small room is
    best, such as a closet or bathroom), and it may be necessary to
    outgas vapors from the walls or wall coverings by heating and
    ventilating the room before it is used with the heaters. FIR
    heating seems to help people most who feel cold, and who have
    orthostatic intolerance (and thus cannot tolerate other ways of
    heating the body, such as hot showers, without feeling faint).
    Considerable water and minerals are lost in the sweat during FIR
    heating, so it is important to replace them by drinking lots of
    water before and during the heating, and also to take enough of a
    good multimineral supplement. Replenishment of magnesium and zinc
    is particularly important. This heating often feels very pleasant,
    and it is easy to overdo it, so care must be taken to approach this
    gently. If a PWC begins to feel worse after undertaking a program of
    FIR heating, she or he should try backing off on the total amount of
    time it is used per week, and/or increasing the intake of water
    and/or minerals.

    11. Removal of Heavy Metals

    Many PWCs have accumulated considerable body burdens of toxic heavy
    metals, again because of their longstanding glutathione deficit. One
    heavy metal that is very commonly elevated is mercury, because of
    its constant evaporation and corrosion from amalgam fillings in the
    teeth, and because of the consumption of large predatory fish,
    including tuna.

    It is important to test for heavy metals before initiating efforts
    to remove them. I suggest a combination of hair testing (as for
    example by Doctor's Data Laboratories) and urine testing after
    challenge by a chelating agent such as DMSA (succimer) (as offered
    by the King James Laboratory in Ohio, for example). Blood and stool
    tests are also available, and there are proponents for each.

    If excessive mercury is found, its removal from the body must be
    done very carefully, because otherwise it is possible to mobilize it
    and transfer it into the brain and nervous system, where it acts as
    a neurotoxin.

    In the field of toxicology, one of the time-honored principles in
    treating toxicity is to first remove the source of the toxin. This
    has led many PWCs, when they became aware of the sources of mercury
    in their teeth, to rush to have their amalgam fillings removed.
    Based on the unpleasant experiences of several who have done this, I
    suggest that it is important first to properly build up the
    detoxication system as described above, so that mercury that is
    released to the body during the removal of the amalgams can be
    properly dealt with. In addition, it is important to select a
    dentist who uses measures for minimizing the mercury exposure of the
    patient from this procedure, such as abundant water cooling to keep
    the amalgam material cool during drilling, a high volume air suction
    device to remove mercury vapor to prevent its inhalation, and a dam
    to prevent the swallowing of mercury-containing material.

    There are several agents available for chelation of mercury. I
    recommend that an experienced specialist in this field be consulted,
    since there are many pitfalls.

    12. Inflammation and Local Extracellular Bacterial Infections

    Many PWCs are suffering from inflammation and local infections. I
    believe that these are exacerbated by the low output of cortisol in
    many PWCs after their onset, as a result of HPA axis malfunction.
    These infections should be sought out, based on the PWCs medical
    history and symptoms, and by specific testing of suspicious areas.
    Common examples are infected root canals, infected cavitations where
    teeth have been pulled, sinus infections, and infections in the
    nasal passages. Problems in the teeth and gums may require removing
    teeth or cleaning out cavitations. An experienced oral surgeon is
    needed for this. Sinus infections can be bacterial or fungal or
    both, and may need to be treated with both antibiotics and
    antifungals. Coagulase-negative staphylococci, which used to be
    considered innocuous, may not be so for PWCs, and may need to be
    treated with a combination of antibiotics. Pioneering work in this
    area has been done by Neil McGregor, Ph.D., in Australia, and by
    Ritchie Shoemaker, M.D., in Maryland. Testing for coagulase-
    negative staphylococcus is not routinely done, but is available from
    Esoterix (www.esoterix.com) by culturing of deep nasal swabs.

    13. Viral and Intracellular Bacterial Infections

    In CFS, it is commonly observed that the immune response has been
    shifted to the Th2 mode, away from the Th1 mode. I think this
    results from long-term elevated cortisol prior to onset, followed by
    glutathione depletion. Some pathogens are also able to promote this
    continuing shift in their own self interest. Because of this shift
    PWCs are particularly vulnerable to viral and intracellular
    bacterial infections, which require a viable Th1 response for their
    defeat. Many of the viral infections found in PWCs appear to result
    from reactivation of latent endogenous viruses of the herpes family.

    Testing should be done for Epstein--Barr virus, cytomegalovirus, HHV-
    6, mycoplasma, and Chlamydia as a minimum, as these are most
    commonly found in CFS. PCR testing for these pathogens and others
    found in CFS is performed by www.mdlab.com.

    David Berg of Hemex Labs in Phoenix has pointed out that in many
    PWCs there are genetic variations in proteins of the blood clotting
    cascade that lead to hypercoagulation when the immune system
    responds to infections. His lab offers tests for this condition.
    If present, hypercoagulation can be countered by low dose heparin
    and by nonpharmaceutical substances such as lumbrokinase and
    nattokinase. It is very important not to counter only the
    hypercoagulation alone, but also to simultaneously combat the
    infectious agent involved. Otherwise, the infection can become
    worse, as can the hypercoagulation in response to it.

    Most of these infections are suppressed by a healthy immune system,
    and Paul Cheney, M.D. reported that glutathione rebuilding was
    effective for restoring the ability of the immune system to put them
    down. In addition, many herpes family viruses can be suppressed by
    taking 3 grams of L-lysine per day, and avoiding foods that are high
    in arginine, such as chocolate and nuts. Nonpharmaceutical antiviral
    substances include oil of oregano and olive leaf extract. There are
    also pharmaceutical antivirals that are effective for some of these
    viruses. Antibiotics can be used to treat mycoplasma and Chlamydia
    infections.

    Some PWCs have viral infections in the brain, i.e. viral
    encephalitides. These are difficult to knock out, but some are
    treatable with existing antivirals, as has been shown by Daniel
    Peterson, M.D. of Incline Village, NV. Testing for these infections
    involves performing analyses, including PCR analyses, on spinal
    fluid taken from a spinal tap (lumbar puncture). PCRs who have
    pressure-type headaches and a variety of neurological symptoms are
    suspects for having encephalitides.

    Transfer factors (such as are available from www.immunesupport.com)
    are another approach that has been found effective in suppressing
    viral infections in PWCs. Joseph Brewer, M.D., of Kansas City has
    reported success with transfer factors against HHV-6 infections.

    As mentioned in the Application section, another very important
    pathogen to test for is Borrellia Burgdorferi, the spirochete that
    is responsible for Lyme disease. It is important also to test for
    other tick-borne disease, such as babesiosis and erlichiosis. This
    is especially important for PWCs who have spent time in brushy or
    wooded areas where deer and mice live. Up to this point, there have
    not been completely reliable tests to distinguish between long-term
    disseminated Lyme disease and CFS, but clinicians should consider
    the tests offered by www.igenex.com and by
    www.immunoscienceslab.com, together with use of clinical diagnosis.
    It remains to be seen whether the new test recently announced by the
    NIH will prove to be more reliable than past tests.

    14. Supporting the Immune System

    To achieve long-term control of infections, it is necessary to have
    a healthy immune system. Supply of the essential nutrients for the
    proper operation of the immune system has been covered in the
    section on Diet and Nutrition. The replenishment of glutathione,
    which is also very important for the immune system, has also been
    covered above. The elimination of inflammation, bacterial
    infections, and the suppression of viral and intracellular bacterial
    infections will go a long way toward taking the load off the immune
    system, and this has also been discussed above. The neuroendocrine
    system, which has significant effects on the immune system, is
    discussed in the next section. Because of the interactions between
    them, these two systems should be supported simultaneously. If the
    immune system continues to be shifted to the Th2 immune response, it
    may be necessary to rebalance it, by using immune modulators such as
    Isoprinosine (Imunovir), MGN-3, Moducare or Pinextra. The goal is to
    restore the immune system's ability to respond either with a Th1 or
    a Th2 response, whichever is needed to combat the threat. There
    have been reports that cimetidine (Tagamet) is effective in enabling
    the immune system to overcome suppression of Th1 (cell-mediated)
    immunity by blocking the histamine H2 receptors on cells of the
    immune system that the pathogens use to fool the immune system.
    (Since cimetidine suppresses the production of stomach acid for
    several hours, it is best taken at bedtime, on an empty stomach. It
    also suppresses phase I detox for some drugs, and may have other
    side effects which should be taken into account.) ProBoost thymic
    protein A (available from www.immunesupport.com) may be helpful
    here, too, since it promotes the production of new helper T cells by
    the thymus gland. Glutamine is another substance that may help here,
    because it is the main food for the lymphocytes. It is necessary to
    take a large dosage to supply it to the lymphocytes, because it's
    also the main food for the intestinal cells, and they have first
    access to it. Some PWCs react unfavorably to glutamine (probably
    because of a leaky blood-brain barrier that allows too much of it
    into the brain to form glutamic acid, the main excitatory
    neurotransmitter). Therefore, it is a good idea to start with a low
    dosage and work up to as much as 20 grams per day if it is tolerated
    well. Bulk glutamine powder is available from www.beyond-a-
    century.com, and it has a sweet taste, so it isn't hard to take.

    It may not be possible to restore the immune system to complete
    health until the HPA axis is dealt with, as described under the
    neuroendocrine system in the next section, because cortisol and DHEA
    are important to the operation of the immune system.

    As part of the immune system balancing, it's also necessary to deal
    with allergies, because they will tend to exhaust the immune system
    and keep it shifted to Th2. It's important to identify the
    substances that produce allergic reactions or sensitivities, and to
    avoid them. Detailed allergy testing should include both the RAST
    test and the Elisa-ACT test. If these are not feasible for a
    particular PWC, elimination of the major causes of food allergies
    and sensitivities can be tried. Elimination from the diet should
    extend for at least two weeks. The major causes are dairy products
    and wheat.

    Hopefully, the leaky gut condition has been dealt with in section 8
    above, and that will have eliminated food intolerances, which also
    place a load on the immune system.

    Another approach that has helped to improve the immune system
    function in some PWCs is to perform skin brushing or lymphatic
    massage, to help the flow of the lymph, which carries the immune
    system cells back to the blood stream via the thoracic duct.

    15. The Neuroendocrine System

    The neuroendocrine system is strongly impacted in many PWCs. Prior
    to the onset of CFS, many PWCs were subject to long-term stress, as
    discussed earlier. The body has specific responses to various kinds
    of stress, but it also has nonspecific responses to stress in
    general. The latter involve the hypothalamus-pituitary-adrenal axis
    and the sympathetic nervous system interacting with the adrenal
    medullas. Long-term stress produces long term elevations in the
    secretion of cortisol by the HPA axis and epinephrine by the adrenal
    medullas. This can lead to adrenal fatigue and can contribute to
    the depletion of glutathione by detoxing the adrenochrome that
    results from the oxidation of some of the epinephrine. After onset
    of CFS, in many cases the cortisol secretion is below normal and/or
    has lost its proper circadian variation, and this appears to result
    from problems with the hypothalamus or higher brain centers. The
    mechanism for this is not yet understood, but it may result from the
    effects of long-term cortisol elevation.

    In addition to this, there are thyroid problems in many PWCs, most
    commonly hypothyroidism and Hashimoto's thyroiditis. The thyroid
    produces considerable hydrogen peroxide in the course of
    synthesizing its hormones, and the cells are normally protected from
    this by glutathione. It seems likely that the glutathione depletion
    that occurs in CFS may be responsible for damage to the thyroid
    gland.

    Furthermore, in female PWCs, problems with the levels of the sex
    hormones are commonly found. In particular, estrogen dominance is
    often a problem, especially after menopause. Even though estrogen
    secretion drops considerably in menopause, progesterone secretion
    may drop even more significantly, producing estrogen dominance.
    This was emphasized by the late Dr. John Lee.

    These neuroendocrine problems are best dealt with together, because
    they are interactive.

    Considering first the HPA axis, it is helpful to determine the
    status of this axis by means of an Adrenal Stress Index test which
    is a saliva test that measures the levels of cortisol at several
    times during the day, as well as the DHEA and secretory IgA levels.
    This test is available from www.diagnostechs.com. Based on the
    results of the test, support can be given to the adrenals if needed.
    Dr. James L. Wilson describes this in his book, available at
    www.adrenalfatigue.com. Dr.
    Corsello's book (www.corsello.com) has some helpful advice about
    this, too. In supporting the adrenals, the goal is to give them a
    rest by supplying an exogenous steroid for a time, together with
    nutrients particularly needed by the adrenals, such as pantothenic
    acid and vitamin C, but to avoid using exogenous steroids at too
    high levels or for too long a time, so that the HPA axis does not
    adapt to them and become dependent on them. It is wise to start
    with very low doses of exogenous steroid if a PWC's HPA axis is
    badly suppressed.

    The status of the thyroid should be determined not by measuring only
    the levels of TSH and T4, but also by measuring the level of free
    T3, because many PWCs don't convert T4 to T3 very well. (This may
    result from the fact that the enzymes that perform this conversion
    are selenoenzymes, and selenium forms an intermetallic complex with
    mercury, which is elevated in many PWCs.) In addition, it's wise to
    measure the armpit temperature upon awakening for a few days to see
    if it is running low, and to pay attention to other hypothyroid
    symptoms, such as general tiredness, weight gain, aches and pains in
    the joints and muscles, low sex drive, abdominal bloating, puffy
    face, depression, muscle cramps, constipation, thickened skin, dry
    and pale skin, thin or brittle fingernails, brittle hair, hair loss,
    including loss of the outer parts of the eyebrows, feeling cold even
    in warm temperatures, and a milky discharge from the breasts). In
    CFS, it is often not easy to distinguish between hypothyroidism and
    partial blockades in the metabolism, since there is considerable
    overlap in symptoms. However, if there appears to be a
    constellation of symptoms that are consistent with low thyroid, a
    trial with thyroid hormone should be considered. In particular,
    consideration should be given to Armour thyroid, because it supplies
    both T3 and T4.

    I suggest referring to Dr. Corsello's book (www.corsello.com) for a
    discussion of balancing the female sex hormones.

    16. Repairing Accumulated Damage

    If all these steps have been carried out, and a PWC still hasn't
    fully recovered, the reason may be that there has been damage to
    the organs and tissues by pathogens, toxins and oxidizing free
    radicals during the duration of the illness. There are several
    approaches now being tested to repair this damage. One is injections
    of growth hormone and bovine growth factors, to stimulate the
    production of new cells, including those in the brain. Another is
    live cell
    therapy, which is done in Mexico, and another is stem cell therapy,
    which is new and controversial. Further developments can be
    expected in these areas.

    I hope this general outline is helpful. Please bear in mind that I
    am a researcher, not a licensed physician. My disclosure statement
    is shown below. I request that anyone considering following this
    outline read my disclosures and send me an e-mail stating that you
    have read them, at richvank@a.... Also, I recommend that any PWC
    desiring to follow this outline first have it reviewed by a
    licensed health care provider familiar with their case, and follow
    it under supervision of such a provider.

    Richard A. Van Konynenburg


    Disclosure Statement:

    As of January 1, 2003, a new law became effective in the state
    of California pertaining to the provision of complementary and
    alternative health care services by non-licensed practitioners.

    I do not regard myself nor advertise myself as a practitioner, nor
    do I accept remuneration for providing health care services, but I
    do frequently give suggestions to individuals about complementary
    and alternative health care, primarily via the internet. Since I do
    reside in California, and am not a licensed healthcare provider, I
    want to make sure that I am operating within the spirit of this new
    law. I am therefore providing the following information required by
    the law:

    1. I am not a licensed physician.

    2. The advice and suggestions I give are alternative or
    complementary to healing arts services licensed by the state of
    California.

    3. The services I provide are analyses of cases of chronic
    syndromes and diseases, particularly chronic fatigue syndrome and
    related disorders, and suggestions for dealing with them.

    4. The theory upon which these services are based is
    that it is possible to understand the root causes and disease
    processes of chronic syndromes and diseases by the use of
    biochemistry and physiology, and to deal with them by means that are
    primarily orthomolecular, functional, holistic, naturopathic,
    alternative, or complementary. Use is made of insights gained from
    specialists in treating these disorders and from published research.

    5. I have B.S., M.S., and Ph.D. degrees in Engineering and Applied
    Science from the University of California--Davis. I worked for
    about 30 years in research and development in chemistry, physics,
    materials science and engineering. I have no formal training in the
    biological sciences or health-related fields. Since 1996 I have
    been performing independent study of chronic fatigue syndrome and
    related disorders. I am a member of the American Association for
    Chronic Fatigue Syndrome and the Orthomolecular Health-Medicine
    Society and am a subscriber to the Journal of Chronic Fatigue
    Syndrome. I have attended five professional conferences
    specifically on Chronic Fatigue Syndrome as of this date, as well as
    several other medical conferences.

    The law requires that written acknowledgment be obtained from anyone
    to whom these health care services are provided that he or she has
    been given the above information. Accordingly, I ask that
    anyone who desires to apply this outline to a particular case to
    please acknowledge that you have read the above by so stating in a
    reply sent to me at richvank@a.... Thank you.

    Richard A. Van Konynenburg

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    Take care...

     

    Greg Lunger

    http://www.yogizenartistdude.com

Monday, February 23, 2004

  • Itza new day !!!

    I find in reading these email post I have a deeper understanding of what I am experiencing, and more difinition about it. Which I can use to explain to others about how I am feeling and why.

    With understnding more of what is going on, I know others know what is happening, and I feel more at peace about it.

    This just came in from the Co-Cure email group.

    MAY BE REPOSTED

    The 2002 Chief Medical Officer's Report into ME/CFS officially
    recognised that a number of serious and unusual neurological symptoms
    and signs do sometimes occur in more severely affected people with
    ME/CFS.  These can include double vision, blackouts, atypical
    convulsions/fits, loss of speech, and loss of swallowing
    (ref: www.doh.gov.uk/cmo/cfsmereport/  Section 4.2.1.2 ).

    When these sort of neurological symptoms and/or signs occur, it is
    always important to exclude the possibility of the cause being another
    neurological disorder.  On such condition is Hashimoto's
    encephalopathy - the diagnosis of one particular case I referred to last
    year on the message boards.  This very interesting case involved a
    14-year-old girl whose initial (mis)diagnosis had been severe CFS, along
    with neurological features (including hand tremor, jerking leg movements
    and blurred vision) and a number of thyroid function test anomalies
    consistent with an autoimmune thyroiditis (as occur in Hashimoto's
    encephalopathy).

    Dr Abhijit Chaudhuri and Professor Peter Behan (University of Glasgow)
    have now published a definitive paper on this not uncommon autoimmune
    central nervous system disorder affecting both children and adults which
    always appears to include a significant degree of central fatigue.  The
    paper describes the principle clinical features in 18 such patients:

    - central fatigue in 100%
    - migraine-type headaches in 90%
    - seizures (focal/general/myoclonic) in 67%
    - stupor in the acute presentation in 67%
    - focal neurological deficit in 67%
    - psychosis, delusions or hallucinations in 50%
    - cognitive impairment in 33%
    - alternating hemiparesis (ie loss of use on one side of the body)
      in 16%
    - cerebellar ataxia (ie severe disturbance with balance/co-ordination)
      in 15%

    Dr Chaudhuri and Professor Behan conclude that the range of laboratory
    investigation abnormalities found in these 18 patients (which include
    brain biopsies) indicate that this is an autoimmune disease of the
    central nervous system and so encephalomyelitis is a much more
    appropriate descriptive term than encephalopathy.

    Furthermore, with a prompt diagnosis and appropriate therapy, the
    prognosis for complete recovery from Hashimoto's encephalomyelitis is
    often excellent.

    Reference:
    The clinical spectrum, diagnosis, pathogenesis and treatment of
    Hashimoto's encephalopathy (recurrent acute disseminated
    encephalomyelitis).  Current Medicinal Chemistry, 2003, 10, 1945 - 1953.

    Dr Charles Shepherd
    Medical Adviser, MEA

    ENDS

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    Follow your Passions !

    Take care...

    Greg Lunger

    http://digitalartdude.typepad.com/digital_art/

Sunday, February 22, 2004

  • Here is some good news!

    Federal Rules Do Not Bar Hospitals From Giving Discounts to
    the Uninsured, Bush Administration Says

    Access this story and related links online:
    http://cme.kff.org/Key=1962.TM.C.D.NjrYnj

      In a "toughly worded response" to hospitals, HHS Secretary
    Tommy Thompson on Thursday said that federal regulations do not
    prevent hospitals from offering discounts to uninsured patients,
    the Wall Street Journal reports (Lagnado, Wall Street Journal,
    2/20). In a letter sent to Thompson in December, the American
    Hospital Association asked HHS to change or clarify pricing
    schedule rules so that hospitals can give discounts to uninsured
    patients without worrying about violating Medicare rules.
    According to hospitals, Medicare regulations require them to
    keep a uniform price list for treatments and procedures for all
    patients (Kaiser Daily Health Policy Report, 12/17/03).
    Hospitals often bill the uninsured for "full charges," or the
    list prices that hospitals maintain for every item and
    procedure. Insurance companies and the Medicare and Medicaid
    programs often pay lower rates, the Journal reports. According
    to hospitals, Medicare policy requires "aggressive efforts to
    collect from all patients," including those who are uninsured.
    Hospitals also believed that Medicare policy did not allow
    hospitals to provide discounts to the uninsured. Medical bills
    are the second leading cause of personal bankruptcy, and
    hospitals have "come under fire" for what they charge and what
    tactics they use to collect unpaid bills, the Journal reports
    (Wall Street Journal, 2/20).

    Thompson's Response and Guidelines

    In a letter to AHA President Richard Davidson, Thompson said,
    "Nothing in the Medicare program rules or regulations prohibit
    such discounts" to the uninsured. Thompson also said that
    hospitals should "take action to assist the uninsured and
    underinsured, and therefore end the situation where, as you said
    in your own words, uninsured Americans and others of limited
    means are often billed and required to pay higher charges"
    (Denver Post, 2/20). The letter includes an accompanying
    document with a "road map for hospitals in the form of a
    question-and-answer dialogue," the Journal reports. One of the
    questions asks: "Are hospitals required to take low-income
    patients to court or seize their homes or send claims out to a
    collection agency when those patients don't pay their hospital
    bills?" The answer: "No. Nothing in the Medicare instructions
    requires the hospital to seize a patient's home, take them to
    court, or use a collection agency." It adds that hospitals are
    not required "to engage in any specific level of collection
    effort for Medicare or non-Medicare patients" (Wall Street
    Journal, 2/20). "Hospitals can provide discounts to uninsured
    and underinsured patients who cannot afford their hospital bills
    and to Medicare beneficiaries who cannot afford their Medicare
    cost-sharing obligations," Thompson said (Appleby, USA Today,
    2/20). Dara Corrigan, acting principal deputy inspector general
    at HHS, said that hospitals could reduce or eliminate copayments
    and deductibles that would create financial hardship for a
    Medicare beneficiary. Corrigan said that hospitals can define
    "financial need" based on local costs of living and the
    beneficiary's income, assets and medical bills. She added that
    the hospital's criteria should be applied consistently to all
    patients. Corrigan said that while hospitals can advertise
    discounts available for uninsured patients, they cannot offer
    discounts "as part of any advertisement or solicitation"
    designed to attract Medicare beneficiaries or to generate
    business payable by Medicare or other federal health programs
    (Pear, New York Times, 2/20).

    Hospital Reaction

    Rick Wade, a spokesperson for AHA, said that Thompson's response
    answered only some of AHA's questions, the AP/Las Vegas Sun
    reports. "When a hospital sets a policy on the indigent, it will
    not accommodate every case that comes through a door," Wade said
    (Sherman, AP/Las Vegas Sun, 2/19). Melinda Hatton, AHA vice
    president, said, "It's still not entirely clear what hospitals
    can do to help the working poor," adding, "How much of a
    discount can they give to a family of four with income of more
    than $37,000 a year?" (New York Times, 2/20). Chip Kahn,
    president of the Federation of American Hospitals, said that
    Thompson's letter could be "a useful roadmap." He added that the
    "substantive guidance should help end confusion and enable
    hospitals to continue their efforts to address this problem on
    which we have a shared concern" (Dorschner, Miami Herald, 2/20).
    Laura Wegscheid, a spokesperson for Colorado-based Centura
    Health, said that hospitals are waiting for guidelines on how
    exactly they can provide discounts and financial assistance to
    uninsured patients who have annual incomes higher than the
    federal poverty level; the guidelines are due for release next
    year, the Post reports (Denver Post, 2/20).

    Advocate Reaction

    Elisabeth Benjamin, an attorney for the Legal Aid Society, said
    that Thompson's letter "finally puts to rest the hospitals'
    tired and inaccurate argument that the government made them
    charge uninsured and underinsured people these crazy inflated
    prices" (Wall Street Journal, 2/20). K.B. Forbes, executive
    director of the Council of United Latinos, said, "We are very
    pleased with Secretary Thompson's letter. It's now clear that
    hospitals can offer discounts to the uninsured, including
    working-class families who earn too much to qualify for charity
    care, but not enough to pay their medical bills" (New York
    Times, 2/20). James Tallon, president of the United Hospital
    Fund, said that Thompson's letter is a good "template" because
    "there was ample room for criticism of hospitals' behavior."
    However, he added that "hospitals were genuinely confused by the
    thicket of federal regulations" (Wall Street Journal, 2/20).

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    Take care...

    Greg Lunger

    http://digitalartdude.typepad.com/

The_Phoenix_Within

  • Visit The_Phoenix_Within's Xanga Site
    • Name: Greg
    • Country: United States
    • State: California
    • Birthday: 9/19/1953
    • Gender: Male
    • Member Since: 11/18/2003

About Me

  • Welcome This site is for those who have "Chronic Fatique Syndrome", or have a family member or friend with it. "The Phoenix Within" is to help us live life to the fullest. With CFS only being "part" of our lives. To find our passions...and follow them...live them... My Passion is Art & Photography, Abstract Expressionism and Surreal. My Cyber Gallery is here : http://www.yogizenartistdude.com Come on over and visit ! This is my other Blog, "Digital Art & Photography". http://digitalartdude.typepad.com/ This Blog is listed at "Blogwise". http://www.blogwise.com

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