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Greatest Vitamins World

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by Ellen DuBois on 02/19/12

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Sick and Tired of Aching Joints?

by Ellen DuBois on 01/05/12

Undenatured Type II Collagen - Chicken Soup for Your Joints

by Karen Lee Richards*
Source:
ProHealth.com

Undenatured chicken collagen, the primary ingredient in OsteoTec™ UC·II®, has been shown in studies and trials to help the body repair and rebuild joint cartilage - reducing joint pain, increasing joint mobility and flexibility, and promoting long-term joint health.

Grandmothers around the world have been treating colds with chicken soup for generations; then a few years ago scientists confirmed that several ingredients in chicken soup do, indeed, affect the immune system. What grandma didn't realize, though, is that one part of the chicken in particular may also help ameliorate the joint pain of arthritis.

Taken from the chicken's sternum cartilage, UC·II is an innovative, patented form of undenatured type II collagen that works with the immune system to reduce inflammation and restore cartilage (unlike glucosamine & chondroitin, which are materials involved in the structure of healthy cartilage). Extensive research and clinical studies have shown UC·II to be both safe and effective in supporting joint health - and clarify how it helps the body derail a destructive process involved in both types of arthritis.

Like Grandma's Cold Remedy, UC·II was Discovered in the Kitchen.

Dr. Eugene Moore, a chemical engineer, had an 8-year-old daughter, Anne Marie, who was diagnosed with rheumatoid arthritis. Her swollen and painful joints continued to worsen until, by the time she was in her late 20's, much of her life was spent in an electric wheelchair.

One day Dr. Moore read about some studies on chicken collagen which showed that a small amount taken orally could have a preventive effect on rheumatoid arthritis. Putting his chemical engineering background to work, he went to the grocery, bought some chickens, and turned his kitchen into a laboratory. What Dr. Moore discovered was that, unlike grandma's chicken soup, if he cooked the chicken collagen, it became ineffective. So he formulated a recipe for an 'undenatured' (also called natural or native; not processed by high heat or chemicals) chicken collagen using the chicken's sternum cartilage.

After his daughter's rheumatoid arthritis began to improve, Dr. Moore shared his preparation with his good friend, Roger, who suffered with osteoarthritis so severe he could no longer function normally. Within a few weeks, Roger, too, began to feel and function much better. Both Anne Marie and Roger described the results as extraordinary - a significantly improved quality of life with no side effects.

Since Dr. Moore's initial discovery, a number of other studies have confirmed the benefits of undenatured type II collagen for joint health in both humans and animals.

Trial Shows UC·II More Than Twice as Effective as Glucosamine and Chondroitin

In a randomized, double-blind study of 52 osteoarthritis patients, one group took 40 mg UC·II and the other a combination of 1500 mg glucosamine and 1200 mg chondroitin. (Double-blind means neither the study subjects nor those tracking the results knew which patients were receiving which doses.) The table below shows the results after 90 days (percentages indicate the reduction in symptomatology):

Symptom UC·II G & C
Stiffness and difficulty in physical function 33.3% less 14.0% less
General level of pain 40.4% less 15.4% less
Effect of pain on daily activities 20.2% less 5.9% less

A small daily dosage of UC·II reduced joint pain and increased joint mobility and flexibility significantly - more than twice as much as the larger dosages of glucosamine and chondroitin.(1)

Additional Human Clinical Trials

  • A pilot study looked at five women who had significant joint pain symptoms. Each took 40 mg of UC·II for 42 days. Four of the five reported significant reductions in pain and stiffness. The average reduction in pain level was 26 percent.(2)

  • Six out of 10 rheumatoid arthritis patients reported significant improvement after taking UC·II for three months. One patient experienced complete remission. No side effects were reported.(3)

  • In a 90-day, double-blind, placebo-controlled study, 60 patients with severe, active rheumatoid arthritis were split into two groups. In the half taking UC·II, 28 showed considerable improvement compared to the placebo group. Four patients recovered completely.(3)

  • Ten children (8 to 14 years old) with active juvenile rheumatoid arthritis were given UC·II for three months. Eight of the 10 experienced a reduction in swollen and tender joints and one experienced a complete remission.(4)


Animal Studies

Humans are not the only ones who suffer the pain of arthritis. One in four pet dogs in the U.S. is diagnosed with some form of arthritis, as are millions of horses worldwide. A number of studies have been done using UC·II to treat osteoarthritic dogs and horses, with good results. For example:

  • Osteoarthritic dogs were given either 40 mg of UC·II or a placebo for 120 days. The dogs given the UC·II exhibited significant improvements as measured by detailed observation of pain-related behaviors and responses: 77 percent less evidence of overall pain, 83 percent less evidence of pain after limb manipulation, and 84 percent less pain after exercise. The dogs receiving the placebo exhibited no significant change in observed pain behaviors/responses.(5)

  • Osteoarthritic horses were divided into groups of five or six, receiving either 320 mg of UC·II, 480 mg of UC·II, 640 mg of UC-II, 5,400 mg of glucosamine plus 1,800 mg of chondroitin, or a placebo. The horses who received the 320, 480 or 640 mg of UC·II exhibited significant reductions in arthritic pain. The UC·II dosages of 480 or 640 mg had equal effects - an 88 percent decrease in overall pain and a 78 percent decrease in pain upon limb manipulation. UC·II was found to be more effective than glucosamine plus chondroitin.(6)


How UC·II Works on Rheumatoid Arthritis and Osteoarthritis

Rheumatoid arthritis is an autoimmune disease in which the body's own immune system turns against itself, and killer T-cells begin to attack the joint cartilage, resulting in inflammation and joint destruction.

UC·II contains molecular regions called
epitopes. These are immune system markers that interact with certain antibodies to trigger the deactivation of collagen-specific killer T-cells, and in turn help deactivate the inflammatory process.

Osteoarthritis is characterized by an inflammatory synovial response that leads to joint wear and tear and is usually attributed to aging.

Many of the biochemical markers associated with OA inflammation are also associated with RA inflammation; therefore similar therapies are usually used. Research has shown that UC·II suppresses the T-cell-mediated inflammation in both forms of arthritis.

Denatured vs. Undenatured - Why the Difference Is Important

Denatured (hydrolyzed). As Dr. Moore discovered in his kitchen laboratory, when chicken sternum collagen is heated, it loses its ability to repair and rebuild the joints. Most of the type II chicken collagen found in dietary supplements is denatured or hydrolized, which means that high heat and/or chemicals have been used to process it. These processes fundamentally alter the molecular structure of the protein, rendering the collagen ineffective as an immunomodulator. There are no peer-reviewed scientific studies showing that denatured type II collagen provides any joint health benefits. And in fact one study states, "denatured type II collagen has no observable effect on the incidence and severity of the disease [arthritis]."(7)

Undenatured (native). Undenatured type II collagen is made using little or no heat and very limited processing - just enough to concentrate the collagen and make it soluble. The UC·II manufacturing process ensures that the collagen remains biologically active in its most native, triple helix form, with its immunomodulating ability intact.

The Right Dosage is Essential

Although some people think "if a little is good, more must be better," this definitely does not apply to undenatured type II collagen.

Small amounts have been found to be the most effective in modulating the body's immune response, but too much can produce a negative or opposite result. The daily dosage recommended for maximum effectiveness is 40 mg UC·II (containing 10 mg bioactive undenatured type II collagen).

In addition to the bioactive UC·II undenatured type II collagen,
OsteoTec UC·II contains Aquamin® (mineralized red algae) - a source of calcium plus more than 70 naturally occurring trace minerals absorbed from the sea; clinically proven to improve bone and joint health.(8)

Unique Natural Support for Joint Health & Function

Overall, clinical trials and studies strongly support OsteoTec UC·II's unique ability to work with the immune system naturally, often helping to defuse the destructive inflammatory processes responsible for stiffness and pain in both rheumatoid and osteoarthritis.

You can purchase OsteoTec UC-II at ProHealth.com

Source: ProHealth.com -
"Undenatured Type II Collagen - Chicken Soup for Your Joints"

____
* Karen Lee Richards is the Lead Expert specializing in Fibromyalgia and ME/CFS, for HealthCentral's ChronicPainComnection (
www.chronicpainconnection.com). Karen is co-founder of the National Fibromyalgia Association (NFA) and was Executive Editor of Fibromyalgia AWARE magazine for four years.

References:
1. Bagchi M, et al. Beneficial effects of oral administration of undenatured type-II collagen on osteoarthritis: a human clinical trial. Presented at: Journal of the American College of Nutrition 49th Annual Meeting; October 2008; Arlington, Va. Abstract No. 30. (See also Crowley DC, et al.
Safety and efficacy of undenatured type II collagen in the treatment of osteoarthritis of the knee: A clinical trial. International Journal of Medical Sciences, 2009;6:312-321. November 2009)

2. Bagchi D, et al.
Effects of orally administered undenatured type II collagen against arthritic inflammatory diseases: a mechanistic exploration. Int J Clin Pharmacol Res. 22(3-4):101-10, 2002.

3. Trentham D, et al.
Effects of Oral Administration of Type-II Collagen on Rheumatoid Arthritis. Science. 261:1727-1730, 1993.

4. Barnett, et al.
A Pilot Trial of Oral Type-II Collagen in the Treatment of Juvenile Rheumatoid Arthritis. Arthritis & Rheumatism. 39:623-628, 1996.

5. Gupta RC, et al. Pain reduction measured by ground force plate in arthritic dogs treated with type-II collagen. Presented at: Society of Toxicology 48th Annual Meeting; March 2009. (See also: D'Altilio M, et al. Therapeutic efficacy and safety of undenatured type II collagen singly or in combination with glucosamine and chondroitin in arthritic dogs. Toxicol Mech Methods. 17:189-196, 2007; and Deparle LA, et al.
Efficacy and safety of glycosylated undenatured type-II collagen (UC-II) in therapy of arthritic dogs. J Vet Pharmacol Therap. 28:385-390, 2005.)

6. Gupta RC, et al.
Therapeutic efficacy of undenatured type-II collagen (UC-II) in comparison to glucosamine and chondroitin in arthritic horses. J Vet Pharmacol Therap. 32:577-584, 2009.

7. Nagler-Anderson C, et al.
Suppression of type II collagen-induced arthritis by intragastric administration of soluble type II collagen. Proc Natl Acad Sci USA. 83:7443-7446, 1986.

8. Frestedt, JL, et al.
A Natural mineral supplement [Aquamin] provides relief from knee osteoarthritis symptoms: a randomized controlled pilot trial. Nutrition Journal, 7(9), 2008.

___
Note: This information has not been evaluated by the FDA. It is general and is not meant to prevent, diagnose, treat or cure any condition, illness, or disease. It is very important that you make no change in your healthcare plan or health support regimen without researching and discussing it in collaboration with your professional healthcare team.

 

Super Sweet Vitamin Sale!

by Ellen DuBois on 10/23/11

Vitamin World

 

The Importance of Vitamin D in you life, and the ones you love.


Sunshine Vitamin Has D-lightful Health Benefits

by Karen Lee Richards*
Source: ProHealth.com

When it comes to the family of vitamins, vitamin D stands alone. It is the only vitamin the body can produce on its own. That's because it is actually a hormone. Due to its unique status, vitamin D surpasses all other vitamins in the multitude of health benefits it offers.

Vitamin D was discovered in the early part of the 20th century. Large numbers of children were developing rickets, a softening and weakening of the bones that often caused significant deformity and multiple fractures. When a researcher found that cod liver oil could prevent rickets, he named the nutritional factor in it that promoted calcium deposition, vitamin D.

Since rickets was thought to be another vitamin-deficiency disease like scurvy or beriberi, the cure was given the next letter in the vitamin alphabet, following the already existing A, B and C. We now know that vitamin D should probably never have been labeled a vitamin at all.

Sources of Vitamin D

Vitamin D has long been recognized as the "sunshine vitamin" because it is naturally produced when skin is exposed to sunlight's UVB rays. Actually, exposure to sunlight is the only natural source of significant amounts of vitamin D. However, getting enough sun exposure to produce adequate amounts of vitamin D can be difficult. It can vary greatly depending upon the time of day, season, latitude, age, skin pigmentation and the amount of skin not covered with clothing or sunscreen.

Dietary intake is not a good option for vitamin D because, with the exception of oily fish and fish-liver oil, vitamin D does not naturally occur in food. Milk and other dairy products, orange juice and breakfast cereals have been fortified with small amounts of vitamin D, but it is virtually impossible to get adequate amounts through your diet. It would take 5 cans of tuna, 10 eggs, 10 glasses of milk, or up to 17 cups of breakfast cereal to get 1000 IU of vitamin D.

Because it is so difficult to get adequate amounts of vitamin D from natural sources, supplementation is usually the most practical solution.

Dangers of a D-ficiency

Vitamin D - view details Many years ago it was thought that the only significant danger from a vitamin D deficiency was the development of rickets in children. That is why milk and other foods first began to be fortified with vitamin D as far back as the 1930s. As it turns out, rickets was just the tip of the iceberg.

Next, vitamin D deficiency was found to be a key factor in other bone diseases like osteopenia (thinning bones), osteoporosis (porous, brittle bones), and osteomalacia (a softening of bones in adults, often starting with insidious muscle weakness and aches and pains in the lower back & thighs, later spreading to arms and ribs).

In more recent years scientists have discovered that a vitamin D deficiency may contribute to an even wider variety of health problems. Michael F. Holick, PhD, MD, in a 2006 report in the journal Mayo Clinic Proceedings, stated, "Many lines of research support the concept that inadequate vitamin D may be involved in the pathogenesis and/or progression of several disorders, including cancer, hypertension, cardiovascular disease, neuromuscular diseases, osteoarthritis, diabetes, and other autoimmune diseases."(1)

Who is at Risk for Vitamin D Deficiency?

As it turns out, almost everyone is at risk of having a vitamin D deficiency. A 2009 epidemiological study found that an astounding 77% of Americans have insufficient levels of vitamin D. The numbers are even higher in Europe and higher still in the Middle East, where women especially tend to stay covered when outdoors.(2)

Although virtually everyone has some risk, following are specific groups who have an especially high risk for vitamin D deficiency:

  • Adults over 50 - As we age, the skin cannot synthesize vitamin D as efficiently and the kidney is less able to convert it to its active hormone form.

  • People with limited sun exposure - If you're homebound, wear clothing that covers most of your skin, or live in northern latitudes that get little sunlight part of the year, it's unlikely that you get adequate amounts of vitamin D.

  • People with dark skin - The pigment melanin, which results in darker skin, also reduces the skin's ability to produce vitamin D from exposure to sunlight.

  • People who have fat malabsorption problems - Vitamin D is fat soluble and therefore requires some dietary fat in the gut for absorption. Some medical conditions associated with fat malabsorption include some forms of liver disease, cystic fibrosis and Crohn's disease.

  • Tobacco smokers - Tobacco smoking is associated with significantly reduced vitamin D levels.

  • People who are obese - Greater amounts of subcutaneous fat sequester more of the vitamin D and alter its release into the circulation.

  • People who have had gastric bypass surgery - Part of the upper small intestine where vitamin D is absorbed is bypassed, which may lead to inadequate levels.

Measuring Vitamin D Levels

The only way to know for sure if you are deficient in vitamin D is by a blood test that measures serum 25(OH)D concentrations. 25(OH)D or 25-hydroxyvitamin D is a metabolite of vitamin D. There is considerable disagreement among experts as to exactly what 25(OH)D levels should be. Norms will vary between labs but the following chart will give you a general idea of what to look for: (3)

25(OH)D Concentrations
Severely Deficient < 8 ng/ml
Deficient 8 - 19 ng/ml
Insufficient 20 - 29 ng/ml
Sufficient 30 - 49 ng/ml
Optimal 50 - 99 ng/ml
Excessive 100 - 150 ng/ml
Potentially toxic >150 ng/ml

Vitamin D's Role in Chronic Pain, Fibromyalgia and ME/CFS

An important vitamin D connection that has only recently begun to be recognized and emphasized is the link between low vitamin D and chronic pain. Although a number of experts have recommended that vitamin D deficiency be considered in the differential diagnosis of patients with musculoskeletal pain, fibromyalgia, and ME/CFS, this is still not known - or ignored - by many healthcare professionals.(4)

Following are just a few examples of research examining the role of vitamin D in a variety of pain conditions:

Fibromyalgia: A 2009 study looked at 139 patients with fibromyalgia and/or non-specific musculoskeletal pain. Three-quarters of them were deficient in vitamin D. Following vitamin D supplementation, clinical improvements were observed in 90% of the patients.(5)

Neuropathy (Nerve Damage): A 2008 study examined 51 patients with diabetic neuropathy. After supplementing with approximately 2000 IU of vitamin D each day for three months, there was a 50% decrease in pain scores.(6)

Migraines: Case reports have shown that two months of supplementation with vitamin D combined with calcium dramatically reduced both the frequency and intensity of migraines in post- and pre-menopausal women.(7-8)

Chronic Back Pain: In 2003 researchers studied 360 patients with chronic back pain. After three months of vitamin D supplementation, symptom improvement was seen in 95% of all subjects and in 100% of those who were severely deficient in vitamin D at the start of the study.(9)

Vitamin D Impacts a Wide Range of Illnesses

In addition to chronic pain conditions, a deficiency in vitamin D has been linked to many other illnesses, such as:

Vitamin D - view detailsBone Disease (Osteopenia, Osteoporosis and Osteomalacia): It is widely known that a combination of Vitamin D and calcium supplements can help decrease postmenopausal bone loss and prevent osteoporosis. A major function of vitamin D is to maintain serum calcium concentrations. When vitamin D levels are low, calcium concentrations are inadequate, resulting in bone disease. A 2005 meta-analysis of randomized controlled trials found that oral vitamin D supplementation in the range of 700 to 800 IU/d should reduce the risk of hip or any nonvertebral fracture by approximately 25%.(10)

Colds, Flu and Other Respiratory Tract Infections: Because of reduced sunshine in fall and winter months, a study was undertaken to determine if low vitamin D levels correlated with the incidence of acute viral respiratory tract infections. The researchers found that individuals with a serum 25(OH)D concentration of less than 38 mg/ml were three times more likely to become ill with an acute respiratory tract infection.(11)

Type 2 Diabetes: According to a new study, vitamin D deficiency is highly prevalent in patients with Type 2 diabetes and may be associated with poor blood sugar control. The study, which looked at 124 patients with Type 2 diabetes, found that 91% had a vitamin D deficiency or insufficiency. Investigators also found an inverse relationship between vitamin D levels and hemoglobin A1c values - those with lower vitamin D levels had higher A1c levels. Co-author Esther Krug, MD, concluded, "This finding supports an active role of vitamin D in the development of Type 2 diabetes."(12)

Rheumatic Conditions (Rheumatoid Arthritis, Osteoporosis, Osteoarthritis, etc.): Two new studies have shown that vitamin D deficiency is common in patients with a range of rheumatic diseases.

  • A UK study showed that 58% of individuals with a rheumatic condition had low vitamin D levels,

  • An Italian study reported that 85% of rheumatic patients not taking vitamin D supplements had insufficient levels - as did 60% of those who were taking recommended doses of vitamin D.
A third study assessing response to vitamin D supplementation found that taking the traditionally recommended daily dose did not normalize vitamin D levels in rheumatic disease patients, indicating that higher doses would probably be necessary.(13)

Cardiovascular Disease: Noticing that people in sun-deprived regions suffered more heart attacks than did those in sunnier locales, scientists began to suspect that vitamin D may have some relationship to cardiovascular health. Investigating that theory, New Zealand researchers found that people who had suffered heart attacks had significantly lower vitamin D levels than controls who had no heart attacks. (14)

A few years later, UK researchers conducted an exhaustive worldwide study that demonstrated a consistent relationship between sunlight exposure and heart disease. The further north people lived, the more frequently they experienced heart attacks, suggesting that vitamin D, which is activated by sunlight, reduces the risk of heart disease.(15)

Multiple Sclerosis: Several epidemiological studies have shown that exposure to sunlight during early life may have a protective effect regarding the development of multiple sclerosis in later years. And a recent longitudinal study confirmed that vitamin D supplementation reduced the life-time prevalence of MS in women. It is thought that the white matter of the brain affected by MS contains vitamin D receptors, and that inadequate vitamin D in the early years of life may predispose these cells to an early death.(16)

A new 2010 retrospective study also found that lower vitamin D levels are associated with a substantially increased relapse rate in pediatric-onset multiple sclerosis.(17)

What Kind of Vitamin D Should You Take?

There are two main types of vitamin D - D2 (ergocalciferol) and D3 (cholecalciferol). The best supplement to take is vitamin D3 because it is the form that also is produced naturally in the skin from sun exposure. Vitamin D2 is produced by irradiating fungi, and is less efficient as a precursor to the active vitamin D metabolite calcitriol.(18)

How Much Vitamin D Is Enough? ...Too Much?

The recommended dosages of vitamin D are currently in the state of flux due to the abundance of new and on-going research on the subject. Ever aware of their ethical precept, "First, do no harm," clinicians often lean toward recommending the lower levels of supplementation.

The US Institute of Medicine's Food and Nutrition Board is currently revising its recommendations on Vitamin D dosing. It is generally thought that the new recommended dose will be 1,000 IU/day for healthy adults. If you have a vitamin D deficiency-associated disease, however, you will need significantly more.

In his dosing and testing suggestions, Dr. Stewart B. Leavitt of Pain-Topics.org cites the vitamin D recommendations of two practitioners with the Canadian Centre for Integrative Medicine: "Ko and Arseneau note that recommended vitamin D3 dosing for healthy adults by various authorities, such as the Canadian Cancer Society, is 2,000 IU/day.

"Other leading authorities, such as Reinhold Veith, PhD, suggest that oral supplementation is safe for infants at 1,000 IU/day, for children at 2,000 IU/day, and for adults at 4,000 IU/day. More aggressive dosing (up to 10,000 IU/day) may be useful but should be checked with more frequent lab testing (every 3 months)."(18)

There also continues to be a great deal of disagreement among medical professionals as to the maximum safe dosage. The current "official" limit is 2000 IU/day, but the Vitamin D Council insists that doses up to 10,000 IU/day are not toxic.

One protocol successfully used by many doctors if you are deficient in vitamin D is to take 50,000 IU/week for approximately three months or until your 25(OH)D levels are in the optimal range - and then switch to a maintenance dose of 2,000 IU/day. Of course, having your 25(OH)D serum levels checked regularly is the best way to ensure you are taking the right dose of vitamin D for you.

To find out more about ProHealth's comprehensive line of Vitamin D3 products (and get FREE SHIPPING thru 8/31/10), visit our online store.

Source: ProHealth.com - "Sunshine Vitamin Has D-lightful Health Benefits"



References:

1. Holick MF. High Prevalence of Vitamin D Inadequacy and Implications for Health. Mayo Clinic Proceedings. March 2006, vol. 81 no. 3 353-373.

2. Ginde AA, et al. Demographic Differences and Trends of Vitamin D Insufficiency in the US Population, 1988–2004. Arch Intern Med. 2009;169(6):626-632.

3. Miller DW. Vitamin D in a New Light. LewRockwell.com. September 10, 2007.

4. Shinchuk L, Holick MF. Vitamin D and rehabilitation: improving functional outcomes. Nutr Clin Prac. 2007;22(3):297-304.

5. Badsha H, et al. Myalgias or non-specific muscle pain in Arab or Indo-Pakistani patients may indicate vitamin D deficiency. Clin Rheumatol. 2009;28(8):971-973.

6. Lee P, Chen R. Vitamin D as an analgesic for patients with type 2 diabetes and neuropathic pain. Arch Intern Med. 2008;168(7):771-772.

7. Thys-Jacobs S. Alleviation of migraine with therapeutic vitamin D and calcium. Headache. 1994a;34(10)590-592.

8. Thys-Jacobs S. Vitamin D and calcium in menstrual migraine. Headache. 1994b;34(9)544-546.

9. Al Faraj S, Al Mutairi K. Vitamin D deficiency and chronic low back pain in Saudi Arabia. Spine 2003;28:177-179.

10. Bischoff-Ferrari HA, Willett WC, Wong JB, et al. Fracture prevention with vitamin D supplementation: a meta-analysis of randomized controlled trials. JAMA. 2005 May 11;293(18):2257-64.

11. Savetta JR, et al. Serum 25-Hydroxyvitamin D and the Incidence of Acute Viral Respiratory Tract Infections in Healthy Adults. PloS One, Jun 14, 2010. doi:10.1371/journal.pone.0011088.

12. Endocrine Society News Release, June 21, 2010. (Study details to be presented June 26, 2010 at The Endocrine Society’s Annual Meeting in San Diego.)

13. Vitamin D deficiency confirmed as common across a range of rheumatic conditions: Recommended supplementation is not sufficient to normalize vitamin D levels in RA and osteoporosis patients. (Studies presented June 18 at EULAR 2010, the Annual Congress of the European League Against Rheumatism in Rome, Italy.)

14. Scragg R, et al. Myocardial infarction is inversely associated with plasma 25-hydroxyvitamin D3 levels: a community-based study. Int J Epidemiol. 1990 Sep;19(3):559-63.

15. Grimes DS, Hindle E, Dyer T. PDF: Sunlight, cholesterol and coronary heart disease. QJM. 1996 Aug;89(8):579-89.

16. Chaudhuri A. Why we should offer routine vitamin D supplementation in pregnancy and childhood to prevent multiple sclerosis. Med Hypotheses. 2005;64(3):608-18.

17. Mowry EM, et al. Vitamin D status is associated with relapse rate in pediatric-onset multiple sclerosis. Annals of Neurology, May 2010; 67(5):618-24.

18. Leavitt SB. Vitamin D for Pain: Dosing and Testing Suggestions. Pain-Topics.org. June 4, 2010.
___

* Karen Lee Richards is Lead Expert specializing in Fibromyalgia and ME/CFS for HealthCentral's ChronicPainConnection (www.chronicpainconnection.com). Karen is co-founder of the National Fibromyalgia Association (NFA) and was Executive Editor of Fibromyalgia AWARE magazine for four years.

Note: This information has not been evaluated by the FDA. It is general and is not intended to prevent, diagnose, treat or cure any illness, condition, or disease. It is very important that you make no change in your healthcare plan or health support regimen without researching and discussing it in collaboration with your professional healthcare team.



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