Q Sciences Lowers Enrollment Fee!

Q Sciences Lowers Enrollment Fee!

10543427-join-us-vector-buttonAs a result of our continued growth, Q Sciences is making it even easier to become an IBO! During the month of September, Q Sciences will be lowering the enrollment fee from $99.95 to $49.95.

With this new low price you receive a Q Sciences’ Welcome Kit, as well as access to your MyQXLife personal website and dynamic back office, access to Micronutrient Support, a PROPAY Card for commission payments, an EMPowerplus™ Q96 7-Day Sample Box, and the AMOR program with an active AutoShip. Take advantage of this special enrollment pricing by sharing the Q with your family, friends, and prospects!





Just look what you get for that low price!!


IBO Membership – $49.95

* MyQXLife Website and Back Office

* Access to Micronutrient Support

* PROPAY Card for commission payments

* Q Sciences’ Welcome Kit

* EMPowerplus™ Q96 7-Day Sample Box


Looking forward to talking with you and working with you to build a solid Q Sciences foundation.

Charm Brewer

Q Sciences IBO23101179-join-us-here-and-now-banner-or-registration-for-membership-icon-or-sign-do-it-today-and-become-a-mem

Q Omega 3 ~ 61 Health Benefits of Omega 3 fatty acids

Q Omegas

Q Omegas supercharge the natural benefits of essential omega-3 fatty acids, which are necessary nutrients for promoting and maintaining optimum health. By improving digestion, absorption, metabolism, and potency at the cellular level, Q Omegas deliver optimal wellness and support to numerous body systems.

Supplement Facts




61 Health Benefits of Omega 3 fatty acids

  1. There is strong evidence that omega-3 fatty acids have a beneficial effect in bipolar disorder.
  2. Omega-3 fatty acid supplementation is associated with reduced mania and depression in juvenile bipolar disorder.
  3. Clinical studies have reported that oral fish oil supplementation has beneficial effects in rheumatoid arthritis and among some asthmatics.
  4. Fish oil improves tubular dysfunction, lipid profiles and oxidative stress in patients with IgA nephropathy.
  5. Dietary supplementation with flaxseed oil lowers blood pressure in dyslipidaemic patients.
  6. Omega 3 fatty acids improve the cardiovascular risk profile of subjects with metabolic syndrome, including markers of inflammation and auto-immunity.
  7. Omega-3 in modest doses reduces cardiac deaths, and in high doses reduces nonfatal cardiovascular events.
  8. Dietary supplementation with omega-3 fatty acids reduces the incidence of sudden cardiac death in patients with myocardial infarction.
  9. Omega-3 fatty acid reduce the total mortality and sudden death in patients with left ventricular systolic dysfunction.
  10. Raising blood levels of omega-3 fatty acid levels may be 8 times effective than distributing automated external defibrillators (AEDs), and 2 times more effective than implanting implanting cardioverter defibrillators (ICDs) in preventing sudden death.
  11. Omega-3 fatty acid supplementation reduces total mortality and sudden death in patients who have already had a heart attack.
  12. Consuming small quantities of fish is associated with a reduction in coronary heart disease.
  13. Omega-3 fatty acids and vitamin D supplementation results in a substantial reduction in coronary calcium scores and slowed plaque growth.
  14. Omega-3 fatty acids prevent atrial fibrillation after coronary artery bypass surgery.
  15. Omega-3 fatty acid supplementation has a therapeutic effect in children with ADHD.
  16. A combination of omega-3 and omega-6 fatty acids as well as magnesium and zinc consumption provide a beneficial effect on attentional, behavioural, and emotional problems of children and adolescents.
  17. Fish oil supplementation has a significant therapeutic effect on children with autism.
  18. Omega-3 fatty acids appear to be an effective treatment for children with autism.
  19. The consumption of omega-3 fatty acid supplements decreases homocysteine levels in diabetic patients.
  20. Omega-3 fatty acids improve macro- and microvascular function in subjects with type 2 diabetes mellitus.
  21. In patients with stable coronary artery disease, an independent and inverse association exists between n-3 fatty acid levels and inflammatory biomarkers.
  22. Omega-3 fatty acids improve endothelial function in peripheral arterial disease.
  23. Fish oil has a beneficial effect on blood viscosity in peripheral vascular disease.
  24. Fish oil supplementation improves walking distance in peripheral arterial disease.
  25. The omega-3 fatty acid docosapentaenoic acid (DPA) reduces the risk of peripheral arterial disease associated with smoking.
  26. An 8-month treatment with omega-3 fatty acids (EPA and DHA) has a positive effects, such as decreasing inflammation, in patients with cystic fibrosis.
  27. Omega-3 fatty acids may have a protective effect against mucus over-production caused by pulmonary bacterial colonization in cystic fibrosis.
  28. Omega-3 fatty acid supplementation reduces inflammatory biomarkers, erythrocyte sedimentation rate, and interleukin-8 concentrations in cystic fibrosis patients.
  29. DHA increases resistance to Pseudomonas aeruginosa infection.
  30. EPA supplementation has therapeutic value in the treatment of chronic hepatitis C patients.
  31. EPA and DHA have therapeutic value in the treatment of systemic lupus erythmeatosus.
  32. Omega-3 fish oil reduces the severity of symptoms in patients with systemic lupus erythematosus.
  33. Fish and long-chain omega-3 fatty acid intake reduce the risk of coronary heart disease and total mortality in diabetic women.
  34. Higher plasma concentrations of EPA and DPA are associated with a lower risk of nonfatal myocardial infarction among women.
  35. Omega-3 fatty acid consumption is inversely associated with incidence of hypertension.
  36. Fish oil, but not flaxseed oil, decreases inflammation and prevents pressure overload-induced cardiac dysfunction.
  37. The consumption of fish reduces the risk of ischemic stroke in elderly individuals.
  38. A moderate intake of EPA and DHA may postpone cognitive decline in elderly men.
  39. Omega-3 fatty acids may have a therapeutic effect on postpartum depression.
  40. Omega-3 fatty acids may have therapeutic value in the treatment of dry eye syndrome.
  41. Omega-3 fatty acid supplementation exhibits therapeutic value in the treatment of children with attention-deficit/hyperactivity disorder (ADHD) symptomatology.
  42. Fish consumption reduces the risk of ischemic stroke in men.
  43. Omega-3 Fatty acids supplementation prevents and reverses insulin resistance.
  44. Omega-3 fatty acids prevent the formation of urinary calcium oxalate stone formation.
  45. Omega-3 fatty acids are beneficial for children with bronchial asthma.
  46. Omega 3 fatty acid supplementation may contribute to the prevention of early preterm birth in both low-risk and high-risk pregnancies.
  47. Fish consumption is associated with a 63% reduction in prostate cancer – specific mortality.
  48. Omega 3 fatty acids decrease the severity of autoimmune disorders.
  49. Eicosapentaenoic acid (EPA) may have a therapeutic role in attenuating pulmonary hypertension.
  50. Omega-3 fatty acids resulted in an improvement in weight bearing in dogs with osteoarthritis.
  51. Primary open-angle glaucoma patients have reduced blood levels of DHA and EPA.
  52. Omega-3 fatty acids alleviate insulin resistance and fatty liver in obese mice.
  53. Intake of eicosapentaenoic and docosahexaenoic acids from fish may be associated with a reduced prevalence of allergic rhinitis.
  54. Cod liver oil (omega-3 Fatty Acids) reduces the need for NSAIDs in patients with rheumatoid arthritis.
  55. Omega-3 Fatty Acids has significant therapeutic benefits and drug sparing activity in the treatment of rheumatoid arthritis.
  56. Diets containing EPA and DHA have an inhibitory effect on breast cancer growth and metastasis.
  57. Dietary Omega-3 fatty acids may protect smokers against chronic obstructive pulmonary disease (COPD).
  58. Omega-3 fatty acids were shown to be more effective than placebo for depression in both adults and children in small controlled studies and in an open study of bipolar depression.
  59. The omega-3 fatty acid EPA is as effective as fluoxetine (Prozac) in treating major depressive disorder.
  60. A diet low in trans-unsaturated fat and rich in omega-3 fatty acids and olive oil may reduce the risk of age-related macular degeneration.
  61. Higher intake of omega 3 fatty acids may reduce the risk of pneumonia.



Any Questions please ask Charm Brewer Q Sciences IBO


Q Sciences announces their New Meal Replacement shake! Nothing else compares.

eQuivalent+ with Xanthones!!


Last week, Q Sciences announced the launch of a new meal replacement formula: eQuivalent+ with Xanthones.

This product comes in chocolate and vanilla flavors, and can be mixed with water, milk or other liquids for a healthy shake packed with nutrients and protein.  I Love adding strawberries to my shakes!


During last week’s product call, Dr. Kimberley discussed the philosophy behind eQuivalent+, as well as how it fits into the existing Q Sciences product lineup. “When we talk about meal replacements, some of us might think about products like Instant Breakfast, which are often just a pile of chemicals,” said Dr. Kimberley. “This is totally at the other end of the spectrum. This provides the cream of the crop nutrients that you need for an instant meal.” “We formulated this product so that it is compatible with EMPowerplus Q96Qssentials, QBiotics and all the other products we offer at Q Sciences.  eQuivalent+ can be used for weight loss, or it can be used by anyone–including children or older people–as a wonderful source of protein and micronutrients that is easily digested and provides energy and stamina,” said Dr. Kimberley.

Dr. Keith Robbins, a chiropractic physician based in Riverton, Utah, and the product’s co-formulator, also joined the call to highlight eight notable features that set eQuivalent+ apart from other meal replacement formulas on the market:

1. Natural ingredients and vitamin sources. “eQuivalent+ contains no artificial colors, sweeteners or flavors, and whole food constituents are used for the vitamin sources whenever possible,” said Dr. Robbins.

2. Vegan compliant and gluten free. eQuivalent+ is gluten free, and compliant for vegetarian and vegan lifestyles.

3. Premium protein blend. Protein sources vary in their bioavailability and the impact they have on our health, Dr. Robbins explained. eQuivalent+ contains a blend of four protein forms that provide the best bioavailability and health benefits. “Our protein source in eQuivalent+ is brown sprouted rice, pea protein, chia protein and hemp protein,” said Dr. Robbins.

4. Coconut oil. “When we use coconut oil, the body utilizes these medium-chain triglycerides as a carbohydrate–meaning the body will use it more readily–but it provides the energy source benefits of a fat,” said Dr. Robbins.

5. L-Carnitine. “We’ve included L-carnitine for fat utilization,” said Dr. Robbins. “One of the great side benefits I’ve seen in using this product in my practice is people losing weight and dropping fat.”

6. Ashwagandha. ”Ashwagandha has been shown to be not only an appetite suppressant, but a mood enhancer,” said Dr. Robbins.

7. Xanthones. eQuivalent+ contains xanthones from mangosteen for added cardiovascular support, healthy inflammatory response, and immune health. 8. B.E.S.T. blend delivery system. A proprietary enzyme and mineral blend helps boost the bioavailability of the vitamins and minerals in eQuivalent+. “B.E.S.T. stands for Bioavailable, Enzyme-Specific Transport,” said Dr. Robbins.

This system helps actually bring the vitamins and minerals contained in eQuivalent+ into the cells for better utilization. It makes it so that our body doesn’t have to work hard to digest this.

equiv1 Both chocolate and vanilla flavors of eQuivalent+ are now available for purchase through IBO Success! 

You will be able to order online soon.  Until then please call IBO Success @ (385) 374-6400. 

Tell them Charm Brewer sent you!  IBO # 10352.


You can check out all the other great products that Q Sciences has to offer by going to my WEBISTE


Q Sciences has partnered with David Hall the inventor of the Cellerciser!

Health and Fitness in Just 10 Minutes a Day!

Cellercise-David HallQ Sciences has partnered with world-renowned innovator David Hall to offer the Cellerciser to our IBOs at a discounted rate. Taking exercise and fitness to the next level, the Cellerciser provides a full-body workout in just 10 minutes a day. Q Sciences is excited to add such an innovative exercise program to its daily regimen of health and wellness products.

For more information on the Cellerciser contact Charm Brewer Q Sciences IBO

During the week of Mach 3rd- March 10th You will need to call into the Q Sciences Office to order your Cellerciser for a  DISCOUNTED Price .

IBO Success @ (385) 374-6400  Please use my name Charm Brewer and IBO Number 10352

As an IBO or a preferred customer at Q Sciences you will be able to purchase the Cellerciser at a discounted rate.

Retail customers will be a bit higher.

Tri-Fold Cellerciser® Kit

KIT Includes:

  • Portable Tri-Fold Cellerciser®
  • Carrying Case w/ built in Dolly
  • Video (DVD)
  • Book
  • Booklet
  • Exercise Chart
  • Intro Kit
  • Balance bar FREE for limited time


   Price: $450.00  when ordered through Q Sciences as an IBO or a Preferred customer.

Half-Fold Cellerciser® Kit plus Balance Bar

Kit includes:

  • Half-Fold Cellerciser®
  • Video (DVD)
  • Book
  • Booklet
  • Exercise Chart
  • Intro Kit
  • Balance Bar


   Price: $350.00 when ordered through Q Sciences as an IBO or a Preferred customer.


Cellercising has many health benefits!  Here’s 30 of them given by Dr. Morton Walker from an article he wrote that was published in the Townsend Letter for Doctors.

1.   Increase balance and coordination
2.   Reduce cardiovascular disease risk
3.   Increase red blood cell production
4.   Aid in lymphatic circulation
5.   Strengthen heart
6.   Lower resting heart rate
7.   Strengthen muscles
8.   Reduce cholesterol levels
9.   Reduce triglyceride levels
10. Stimulate metabolism
11.  Improve vision
12.  Promote growth and repair
13.  Increase breathing capacity
14.  Increased oxygenation of tissues
15.  Tone the glandular system
16.  Increase thyroid output
17.  Expand capacity for fuel storage
18.  Increase muscle vigor
19.  Tone muscle fibers
20.  Reduce headaches
21.   Relieve back pain
22.   Reduce aches & pains from inactivity
23.   Improve digestion and elimination
24.   Allow for deeper, easier sleep
25.   Stimulate mental performance
26.   Stimulate learning process
27.   Lessen PMS symptoms
28.   Improve immune system
29.   Slow the aging process
30.   Reduce chances of obesity


What else does the Cellerciser enhance in your body?

  • Isometric exercise – it tones the body. Specific cells resist “G-Forces” when the angle of the body is changed. Internal organs lift as connective tissue gets stronger. The muscles tone, collagen strengthens and skin gets firmer.
  • Aerobic exercise – it improves cardiovascular fitness and provides more oxygen to the body. For 10 minutes a day, you can increase cardiopulmonary circulation to every cell in your body faster and more efficiently by Cellercising.
  • Calisthenics – it targets specific muscle groups. The DVD from Cellular Health Innovations demonstrates different techniques to target every part of the body, including thighs, knees, hips, buttocks, waist, stomach, arms, chin, and digestion/elimination at the same time.
  • Isotonic exercise – it builds muscle mass and bone density. With Cellercise all cells expand and contract over 100 times per minute. Jumping up and down on the Cellerciser is a full-body weight bearing activity. The body doesn’t want to get shorter, so it adapts by becoming stronger.
  • Flexibility – is typically achieved by stretching. With Cellercise, cells are massaged, tension melts away, circulation and flexibility are increased without stretching. As cell membranes become more flexible, so do all body parts.

Plus, the Cellerciser flexes every muscle over 100 times per minute!


To order your Cellerciser today call IBO Success @ (385) 374-6400

Please use my name Charm Brewer and IBO Number 10352

EMPowerplus Q96™ Proven Effective: The British Journal of Psychiatry

Q Sciences now has 23 Clinical studies on EMPowerplus Q96™

empowerplus-q96-2.jpg EMPowerplus Q96™ Proven Effective:

The British Journal of Psychiatry Reports “Significantly Robust” Improvement in ADHD and Depression         Symptoms, treatment was much more effective than placebo. Researchers at the University of Canterbury in Christchurch New Zealand have found in a double blind study that a nutritional supplement “EMPowerplus Q96™” has significant benefits for adults with psychiatric symptoms of ADHD, depression, hyperactivity, impulsivity and inattention. Dr. Julia Rucklidge and her team of researchers successfully completed the placebo-controlled study, which was published today January 30th in The British Journal of Psychiatry. In the study researchers reported “We demonstrated that micro nutrient treatment induced statistically robust improvements in several indices….” “Specifically, participants taking the micro nutrient formula reported greater improvement in both inattention and hyperactivity/ impulsivity compared with those taking a placebo.” Dr. Rucklidge further reported “Hyperactivity/ impulsivity scores were reduced into the normal non-clinical range with micro nutrient administration but not placebo.” The research publication also identified a major reduction in symptoms of depression (using the MADRS depression rating scale) in those suffering with moderate to severe depression. “A further exploration of the MADRS scores revealed a significant difference favoring the micro nutrient group when a sub sample of those with moderate or severe depression at baseline was examined” According to the researchers 47.6% of the micronutrient group were “much” to “very much improved” over the eight-week study.  Anthony Stephan Co-founder-EMPowerplus Q96


To learn more to view the research and to order or become an IBO Click here

Charm Brewer

Q Sciences IBO

WOW!! New Research Shows Impressive Health Benefits of Melatonin


New Research Shows Impressive Health Benefits By Debra Fulghum Bruce, PhD


New research indicates that melatonin does much more than help people sleep better.  Exciting studies show that melatonin’s multifacited effects may improve treatment outcomes in cancer patients and extend their lives.  Additional applications of melatonin include guarding the nervous system against degenerative diseases – such as Alzheimer’s disease and stroke –  and preventing debilitating migraines.

Melatonin is secreted from the pineal gland deep inside the brain.  For more than a quarter-century, scientists have been intrigued by melatonin’s ability to coordinate the body’s physiological rhythms that help set the brain’s biological clock.

The principal factor affecting melatonin is light, which inhibits the secretion of this hormone.  Darkness has the opposite effect from light, resulting in signaling the pineal gland to increase melatonin secretion.  The normal cycles of melatonin production are altered due to factors including aging, medications, and light exposure at night.  While the long-term health effects of disrupted melatonin secretion are not yet fully known, some scientists have suggested that years of working nights could lead to adverse effects – even cancer.

Fortunately, melatonin supplements can safely and effectively restore balance to the body’s circadian rhythm of this important hormone – helping achieve a restful night’s sleep and keeping your biological clock ticking throughout a long, healthy life span.

Neuroprotective Benefits

Melatonin is a powerful and versatile antioxidant produced within the body.  Melatonin protects both lipids and proteins against damage, and can scavenge some of the most dangerous free radical in the body – including hydroxyl radicals and hydrogen peroxide.  Unlike other antioxidants, melatonin easily diffuses into all cells, and even crosses the blood-brain barrier to protect the delicate brain. 1

Unfortunately, levels of naturally produced melatonin decline with advancing age, leaving older adults with unlimited antioxidant protection against conditions associated with oxidative stress, particularly neurodegenerative diseases. 1 Supplementing with melatonin may thus help older adults enhance their antioxidant protection against some of the most ravaging diseases of aging, such as Alzheimer’s disease, Parkinson’s disease, and stroke.

Melatonin levels are particularily low in patients with Alzheimer’s disease.  Nearly half of affected individuals suffer from sleep disturbances and “sundowning” – increased confusion, agitation, and other symptoms in the afternoon and evening.  2Not surprisingly, melatonin supplementation benefits patients with Alzheimer’s disease by providing sleep and reducing late-day aggravation of symptoms.  Melatonin has also been found to decrease cognitive deterioration in individuals with Alzheimer’s disease, possibly by protecting brain cells from the toxic protein, beta-amyloid. 2


Melatonin may likewise play an important role in assisting patients suffering from Parkinson’s disease.  Parkinson’s disease is associated with the disrupted melatonin secretion in the brain, and supplemental melatonin may help improve sleep efficiency in affected adults. 3 The brain can suffer dramatic, irreparable damage when an individual suffers a stroke.  Utilizing animal models of stroke, scientists have found that melatonin may offer important protection against stroke-related damage and deterioration.  When administered at the time of stroke, melatonin limited the area of brain tissue damage, decreased brain cell death, lessened behavioral deficits,  and reduced the rate of stroke-related death.  These investigators believe that melatonin’s protective actions stem from it’s free-radical-scavenging and antioxidant activities, and suggest that melatonin may hold promise in improving stroke outcomes in humans. 4

Melatonin may help manage one of the leading risk factors for stroke – elevated blood pressure.  While an earlier study reported that hypertensive men taking melatonin experiences reduced nighttime blood pressure, a newer study confirms the same benefit for women. 5 In a randomized, double-blind study, 18 women (aged 47 to 63) with either normal blood pressure or treated high blood pressure received a three-week course of slow release melatonin (3mg) or placebo, one hour before bedtime.  Researchers recorded blood pressure readings for 41 hours at the end of the trial.  While the daytime blood pressure readings remained unchanged compared to placebo, the melatonin treatment significantly drecreased nighttime blood pressure, without modifying heart rate. 6

Fighting Cancer

One of melatonin’s most important applications is in fighting a wide array of cancers, including breast and liver cancers, non-small-cell lung cancer, and brain metastases from solid tumors. 7

When women with metastatic breast cancer who had failed to respond to tamoxifen received melatonin supplements (20mg every evening), they demonstrated an improved response to the chemotherapy drug. more than one quarter of the subjects – whose disease otherwise was expected to progress rapidly – began responding to the chemotherapy treatment.  Most of the women also experienced anxiety relief from the melatonin supplementation. 8 Laboratory studies suggest that melatonin may help fight hormone-responsive breast cancers by inhibiting the aromatase enzyme, which is responsible for the local synthesis of estrogens. 9,10

Emerging research suggests that melatonin may help fight one of the most common malignancies in aging men – prostrate cancer.  In the laboratory, scientists treated androgen-sensitive and androgen-intensive prostate cancer cells with pharmacological concentrations of melatonin.  Treatment with melatonin dramatically reduced the number of prostrate cancer cells, while the remaining cells displayed signs of slowed replication and increased differentiation – characteristics of healthy, non-cancerous cells.  Melatonin may thus hold promise against prostrate cancers, whether they are hormone-sensitive of hormone-insentive.  11

Scientists conducted a meta-analysis of 10 randomized, controlled trials examining melatonin’s effects (alone or as an adjuvant treatment) on patients with various types of cancer.  Supplementation with melatonin reduced the relative risk of death at one year by an impressive 34% – regardless of the type of cancer or the melatonin dosage.  Importantly, no adverse effects were reported. 12

In addition to it’s benefits for cancer survival, melatonin may also help counteract the toxicity of chemotherapy treatment.  Two-hundred-fifty individuals undergoing chemotherapy for advanced cancers of the lung, breast, gastrointestinal tract, or head and neck received chemotherapy, either alone or in combination with melatonin (20 mg/day).  After one year, the melatonin-supplemented individuals demonstrated a higher rate of survival, and were significantly protected against many or the side effects associated with chemotherapy, including decreased platelet count, neurotoxicity, heart damage, mouth sores, and fatigue. 13

Migraine Prevention

jun2007_nu_melatonin_03   A promising study suggests that a migraine sufferers may be able to reduce the frequency and severity of their headaches by using melatonin.  Researchers gave 34 migraine sufferers (29 women and 5 men) a 3-mg dose of melatonin, 30 minutes before bedtime, for three months.  Of the 32 patients who finished the study, more than two thirds experienced at least a 50% reduction in number of headaches per month.  Additionally, the intensity and duration of headaches decreased.  The scientists  believe that melatonin’s anti-inflammatory effect and free-radical-scavenging effects contribute to its headache-relieving benefits. 14


Promoting Healthy Sleep

jun2007_nu_melatonin_04  Obtaining sufficient amounts of quality sleep is an absolute necessity of good health, yet many of us experience sleep difficulties on occasion.  Insomnia occurs due to a variety of factors – ranging from long hours of work or travel to sleep-disruptive conditions, such as urinary frequency and stressful events.  Elderly adults may be particularly susceptible to difficult sleeping and nighttime awakenings, due to the decline in melatonin levels associated with aging. 15  Melatonin can help promote healthy sleep patterns in some people, regardless of the cause of insomnia.

A large analysis revealed several of melatonin’s sleep-enhancing benefits.  Reviewing 15 studies of sleep in healthy adults, scientists noted that melatonin administration significantly reduced sleep latency (the amount of time needed to fall asleep), while boosting sleep efficiency (the percentage of time in bed spent asleep) and increasing total sleep duration. 16

Men with benign prostatic enlargement often experience poor sleep due to nighttime urinary frequency.  Scientists from the United Kingdom found that melatonin may offer an effective solution.  When 20 older men were treated with 2mg of melatonin each day for one month, they experienced a significant decrease in nighttime urination, and reported that their condition was less bothersome than before treatment. 15

Individuals who work the night shift are often chronically tired due to difficulty falling asleep during the daytime.  Supplementing with melatonin has helped improve the length and quality of daytime sleep in these individuals.  These findings demonstrate an important characteristic of melatonin: the hormone exerts its hypnotic (sleep-inducing) and sedative (anxiety-relieving) effects, regardless of dosage time. 7

Traveling to different time zones often leads to the fatigue and insomnia known as jet lag.  Supplementing with melatonin can help prevent or reduce jet lag, particularly when traveling across several time zones.  Melatonin works by helping re-synchronize the body’s circadian rhythms, helping  the traveler adapt to the local time. 7

Dosage and Interactions

Melatonin is used in doses ranging from 0.3 – 5.0 mg to promote sleep, with doses of 1 – 3 mg most common. 17  Studies examing melatonin’s effects on cancer have utilized doses of 3 – 50 mg/day. 7

Melatonin has a sedating effect, which may be magnified by the use of benzodiazepines or other sedating drugs such as antihistamines or antidepressants.  Similarly,  the use of melatonin with valerian, 5-hydroxytryptophan, or alcohol may increase sedation. 17

The bioavailability of oral melatonin is increased by co-administration of the antidepressant drug fluvoxamine (Luvox®). 17  Beta blockers, as well as asprin and other non-steroidal anti-inflammatory drugs, may decrease melatonin production in the body. 17


unnamed  QSleep contains 1.0 mg of melatonin per serving. This specifically proportioned amount of melatonin is gentle enough to not raise melatonin levels in the body higher than are naturally produced when the pineal gland is functioning properly, but sufficient to aid in restful sleep. QSleep also contains 0.75 mg of 5-HTP per serving. 5-HTP (5-Hydroxytryptophan) is a chemical by-product of the protein building block L-tryptophan. It works in the brain and central nervous system to increase the production of serotonin, which affects sleep.

In addition to these three main ingredients, QSleep contains a proprietary herbal extract to help a person stay asleep throughout the night. The proprietary extract includes the following:

Cramp bark: The chemicals in cramp bark seem to decrease muscle spasms. These chemicals may also lower blood pressure and decrease heart rate.*

QSleepFeverfew: The feverfew herb has many uses, but it seems to be effective for preventing migraine headaches, which can interfere with sleep.*

Ginkgo biloba: Ginkgo biloba leaves are generally used to make extracts that improve blood circulation, which might help the brain, eyes, ears, and legs function better.*

Passionflower: The passionflower is a plant often used for insomnia, gastrointestinal (GI) upset related to anxiety or nervousness, generalized anxiety disorder (GAD), and relieving symptoms related to narcotic drug withdrawal. The chemicals in passionflower have been used for calming, sleep inducing, and muscle spasm relieving effects.

Peppermint: Studies have shown that the leaf and oil from the Peppermint plant provide numerous health benefits. It may aid in helping relieve muscle pain, nerve pain, digestive processes, upset stomach, and inflammation.

Skullcap: Although used for many conditions, there is not yet enough scientific evidence to determine whether or not Skullcap is effective for any one condition. Most commonly, skullcap is used for trouble sleeping, anxiety, stroke, and spasms.

Valerian root: Valerian is an herb that has been used for centuries to help with anxiety and act as a sleep aid. It comes from the valerian plant and works particularly well when combined with other herbs including passionflower.

QSleep is a safe, gentle formula that works in tandem with Qssentials by helping your body and mind regenerate properly throughout the night, thus functioning optimally during the daytime hours. The oral spray delivery method works quickly and may be used as needed.

Each tube contains approximately 30 servings.

Recommended Use: Shake gently and spray 6 to 8 times directly into mouth 15 minutes before going to bed.

You can order Q Sleep here at http://q4mentalhealth.myqxlife.com or click on image.

* The statements made on this website have not been evaluated by the FDA. This product is not intended to diagnose, treat, cure, or prevent any disease. The information presented on this site is not a substitution for professional healthcare advice. Always consult your doctor or healthcare practitioner for questions or guidance on medical problems and conditions.


jun2007_nu_melatonin_05  A factor in restorative sleep, melatonin’s benefits extend to neuroprotection and fighting cancer.  Its powerful antioxidant effect offers important enhancements to the brain and nervous system, helping protect against age-related damage.  Most exciting are melatonin’s benefits for cancer patients – relieving anxiety and improving survival from an array of cancers.  Finally, migraine sufferers using melatonin may enjoy a vast decline in the frequency and severity of their headaches – leading to a tremendously improved quality of life.


1. Suzen S. Recent developments of melatonin related antioxidant compounds. Comb Chem High Throughput Screen. 2006 Jul;9(6):409-19.

2. Cardinali DP, Furio AM, Reyes MP. Clinical perspectives for the use of melatonin as a chronobiotic and cytoprotective agent. Ann NY Acad Sci. 2005 Dec;1057:327-36.

3. Srinivasan V, Pandi-Perumal S, Cardinali D, Poeggeler B, Hardeland R. Melatonin in Alzheimer’s disease and other neurodegenerative disorders. Behav Brain Funct. 2006;2(1):15.

4. Reiter RJ, Tan DX, Leon J, Kilic U, Kilic E. When melatonin gets on your nerves: its beneficial actions in experimental models of stroke. Exp Biol Med (Maywood.). 2005 Feb;230(2):104-17.

5. Scheer FA, Van Montfrans GA, van Someren EJ, Mairuhu G, Buijs RM. Daily nighttime melatonin reduces blood pressure in male patients with essential hypertension. Hypertension. 2004 Feb;43(2):192-7.

6. Cagnacci A, Cannoletta M, Renzi A, et al. Prolonged melatonin administration decreases nocturnal blood pressure in women. Am J Hypertens. 2005 Dec;18(12 Pt 1):1614-8.

7. [No authors listed] Melatonin. Monograph. Altern Med Rev. 2005 Dec;10(4):326-36.

8. Lissoni P, Barni S, Meregalli S, et al. Modulation of cancer endocrine therapy by melatonin: a phase II study of tamoxifen plus melatonin in metastatic breast cancer patients progressing under tamoxifen alone. Br J Cancer.1995 Apr;71(4):854-6.

9. Cos S, Gonzalez A, Martinez-Campa C, et al. Estrogen-signaling pathway: a link between breast cancer and melatonin oncostatic actions. Cancer Detect Prev. 2006;30(2):118-28.

10. Sanchez-Barcelo EJ, Cos S, Mediavilla D, et al. Melatonin-estrogen interactions in breast cancer. J Pineal Res. 2005 May;38(4):217-22.

11. Sainz RM, Mayo JC, Tan DX, Leon J, Manchester L, Reiter RJ. Melatonin reduces prostate cancer cell growth leading to neuroendocrine differentiation via a receptor and PKA independent mechanism. Prostate. 2005 Apr 1;63(1):29-43.

12. Mills E, Wu P, Seely D, Guyatt G. Melatonin in the treatment of cancer: a systematic review of randomized controlled trials and meta-analysis. J Pineal Res. 2005 Nov;39(4):360-6.

13. Lissoni P, Barni S, Mandala M, et al. Decreased toxicity and increased efficacy of cancer chemotherapy using the pineal hormone melatonin in metastatic solid tumour patients with poor clinical status. Eur J Cancer. 1999 Nov;35(12):1688-92.

14. Peres MF, Zukerman E, da Cunha TF, Moreira FR, Cipolla-Neto J. Melatonin, 3 mg, is effective for migraine prevention. Neurology. 2004 Aug 24;63(4):757.

15. Drake MJ, Mills IW, Noble JG. Melatonin pharmacotherapy for nocturia in men with benign prostatic enlargement. J Urol. 2004 Mar;171(3):1199-202.

16. Brzezinski A, Vangel MG, Wurtman RJ, et al. Effects of exogenous melatonin on sleep: a meta-analysis. Sleep Med Rev. 2005 Feb;9(1):41-50.

17. Available at: http://www.pdrhealth.com/drug_info/nmdrugprofiles/nutsupdrugs/mel_0286.shtml. Accessed March 16, 2007.

The facts about Vitamin D!

Vitamin D Hormone

Vit­a­min D and Neu­ro­logic Disorders

1454929_10201650474957996_1579948476_nIf you have a neu­ro­logic prob­lem that is severe enough to see a neu­rol­o­gist, you are prob­a­bly not heal­ing your body as per­fectly as you once did. Most peo­ple who are suf­fer­ing from neu­ro­logic prob­lems such as headache, chronic pain, tremor, bal­ance dif­fi­cul­ties, dizzi­ness, depres­sion, stroke, or mem­ory loss also have abnor­mal sleep. Fix­ing the sleep can often fix the neu­ro­logic problem. Why Vit­a­min D? In 2005 one of my patients with daily headache requested a sleep study because she thought she had sleep apnea. Sur­pris­ingly, her headaches went away after a few weeks of using a sleep apnea mask. Because it worked so well for her, I started to per­form sleep stud­ies on all of my headache patients, and real­ized that they all had abnor­mal sleep stud­ies. Then I began to do sleep stud­ies on my patients with other neu­ro­logic prob­lems such as seizures, back pain, dizzi­ness, stroke or bal­ance prob­lems, and most of them also had abnor­mal sleep stud­ies, some­times with­out being aware that their sleep was abnor­mal. After pre­scrib­ing sleep med­ica­tions and sleep apnea masks for sev­eral years, I acci­den­tally dis­cov­ered that most of my patients had abnor­mal sleep because they were vit­a­min D defi­cient. If fix­ing that defi­ciency might help them sleep nor­mally I’d like to do that first before rely­ing on sleep­ing pills, or hav­ing to wear a sleep apnea mask at night. Vit­a­min D is not a vitamin: We’ve been taught that Vit­a­min D is the “bone vit­a­min”, but it is really more of a sun hor­mone. The word “vit­a­min” means “some­thing my body needs that I can’t make, so I must get it from the food”. D hor­mone is instead, a chem­i­cal that we make on our skin from sun expo­sure. It is a hor­mone like thy­roid, estro­gen or testos­terone. Using the proper word “hor­mone” reminds us that it affects mul­ti­ple parts of the body and that it is not “extra”. It is essen­tial to every cell in the body and it is not in the food. It is sup­ple­mented in milk but as a cup of milk has only 100 IU of vit­a­min D you would have to drink 100 cups of milk a day to keep from being D deficient. Why would we make a hor­mone from sun exposure? D hor­mone is unique among our hor­mones because we make it on our skin from a spe­cific wave­length of light, UVB. Our planet is tilted so as we go north or south from the equa­tor there are sea­sons. In the sum­mer we are closer to the sun, in the win­ter, far­ther from the sun. Where there are sea­sons every liv­ing thing has to deal with6 months of good weather and avail­able food, and six months of ter­ri­ble cold and no food. The far­ther we move away from the equa­tor the lessUVB wave­length there is in the win­ter light so our D hor­mone fluc­tu­ates with the sea­sons; it goes higher in the sum­mer and lower in the win­ter. Any ani­mal that can devise a way to eat more and get strong in sum­mer, and eat less and sleep more in the win­ter, will have a bet­ter chance of sur­vival. Every ani­mal on this planet; mam­mals, rep­tiles, birds, fish and insects use this same chem­i­cal, D3 (chole­cal­cif­erol), made on their skin from UVB light, to do just that. D hor­mone affects our weight and appetite: In the sum­mer as we have more sun expo­sure our D hor­mone level climbs to 80 ng/ ml, we eat more calo­ries, and store less. The high D mes­sage is it’s sum­mer it’s time to build our strength. We use our calo­ries to build stronger bod­ies. We sleep fewer hours, but more effi­ciently, with a higher per­cent­age of the total sleep spent in deeper stages of sleep. In the win­ter there is noUVB light so we use the vit­a­min D we made and stored in sum­mer. As it gets used up the blood level falls. The low D mes­sage is; sleep longer, store fat for spring. Our meta­bolic rate goes down (we hiber­nate). As the D level falls the thy­roid hor­mone goes down, we sur­vive the win­ter by sleep­ing more hours and using less energy. The lower D level appears to affect the pop­u­la­tions of bac­te­ria in our intes­tine. Who lives in our intes­tine appears to affect not only our appetite, but also what we do with the calo­ries we eat do we store fat or put it into mus­cle. ( See The Econ­o­mist mag­a­zine August 18, 2012 “The human micro­biome: Me myself, us” for a good expla­na­tion of how our colonic biome affects our weight.) Low D goofs up sleep. Most of the neu­ro­log­i­cal prob­lems my patients have are not directly related to D hor­mone, they are related to the fact that D hor­mone defi­ciency causes sleep dis­or­ders; insom­nia, sleep apnea,REM related apnea, unex­plained awak­en­ings to light sleep, inap­pro­pri­ate body move­ments dur­ing sleep. All of these dis­or­ders keep us from heal­ing our bod­ies dur­ing sleep. When the sleep improves the headaches, seizures, tremor, back pain, bal­ance dif­fi­cul­ties, depres­sion, mem­ory loss, etc. all get bet­ter. (See the sleep hand­out for more detail about why.) What does D hor­mone defi­ciency look like? D hor­mone affects the entire GI tract. There are D recep­tors in our sali­vary glands, our teeth, our esophageal sphinc­ter, and the stom­ach cells that make acid. When the stom­ach sphinc­ter is weak the acid moves up into the esoph­a­gus, where it doesn’t belong, caus­ing acid reflux. The D we make on our skin goes to the liver, then into the bile, it keeps the bile acids dis­solved, pre­vent­ing gall stones from form­ing. Because there are D recep­tors in the islet cells of the pan­creas that make insulin, not enough D may con­tribute to the devel­op­ment of dia­betes. Low vit­a­min D lev­els are related to poor stom­ach emp­ty­ing as well as bloat­ing and con­sti­pa­tion or “irri­ta­ble bowel”. The irri­ta­ble bowel may result from los­ing our “happy, help­ful” bac­te­ria in our lower GI tract. They die off when we don’t sup­ply the vit­a­min D the bac­te­ria also need to sur­vive. Because those same colonic bac­te­ria sup­ply 7/8 of the B vit­a­mins we need on a daily basis, some of my patients have vit­a­min D defi­ciency and sec­ondary B vit­a­min defi­cien­cies. (At least 2 of the B vit­a­mins, B5 and B12, are needed to sleep nor­mally) So there are sec­ondary B vit­a­min defi­cien­cies that may also have to be cor­rected before the sleep will return to normal. Poor sleep causes hyper­ten­sion, heart dis­ease and stroke: Fif­teen years ago the sleep dis­or­ders experts began to report that every Amer­i­can with high blood pres­sure had a sleep dis­or­der in the back­ground. There­fore the real killer in Amer­ica is not the long term effects of hyper­ten­sion, but the long term effects of abnor­mal, non-restorative sleep. Vit­a­min D appears to affect our sleep cycles through D recep­tors in the low­est part of the brain called the “brain­stem”, where we con­trol the tim­ing and paral­y­sis of sleep. Sleep occurs every night to allow us to heal and make repairs. It is dur­ing sleep that we make the chem­i­cals that keep our blood pres­sure nor­mal dur­ing the fol­low­ing day. While we sleep our arter­ies repair and stay smooth so they don’t have the cho­les­terol build up that closes off the ves­sels lead­ing to heart attack and stroke. The pace­maker cells in the heart heal so we don’t get atrial fib­ril­la­tion that can lead to strokes. Poor sleep causes mem­ory prob­lems and depression: While we sleep we make per­ma­nent mem­o­ries. Dur­ing sleep we also make the sero­tonin that we use dur­ing the day to stay happy and curi­ous, so low D hor­mone can cause depres­sion and mem­ory problems. Low D affects all the blood cells and can cause ane­mia, autoim­mune dis­ease and cancer: There are D hor­mone recep­tors on the red and white blood cells. When the white blood cells don’t have enough D they get con­fused, they start attack­ing our body by mis­take. All of the autoim­mune dis­eases: mul­ti­ple scle­ro­sis, lupus, rheuma­toid arthri­tis, pso­ri­a­sis, and ulcer­a­tive col­i­tis, are related to low D hor­mone. Our own white blood cells travel through our bod­ies at night seek­ing out and killing can­cer cells. Thus, increases in breast, colon and prostate can­cer are also believed to be related to low D. Women with breast can­cer who are told they “can’t take hor­mones”, (mean­ing estro­gen), should still take D hor­mone. The right D level (in addi­tion to nor­mal sleep) helps the body’s own immune sys­tem fight cancer. D hor­mone, bones and calcium: Even though most of us have been told we need extra cal­cium, D defi­ciency is what causes osteo­poro­sis. D helps the GI tract absorb cal­cium and keeps the cal­cium from leak­ing into the urine, (so low D may also cause kid­ney stones by dump­ing more cal­cium than nor­mal into the urine). If the vit­a­min D level is kept 60–80 cal­cium is prop­erly absorbed from the diet and Fos­amax, Evista, Boniva are not needed to pre­vent bone loss. Low D causes bal­ance dif­fi­cul­ties and pain: D defi­ciency can also cause leg pain, burn­ing in the feet, and dif­fi­culty with bal­ance, prob­a­bly through sec­ondary B defi­cien­cies of B12, B5 or B6. Poor sleep results in body pain on awak­en­ing; fibromyal­gia, arthri­tis, chronic low back pain, knee pain, hip pain. Every mov­ing part of the body must get per­fectly par­a­lyzed to repair at night. If paral­y­sis does not occur cor­rectly dur­ing sleep the body doesn’t heal and morn­ing pain can result. Low D causes infer­til­ity, poly­cys­tic ovary syn­drome and endometriosis: There are vit­a­min D recep­tors in the ovaries, the tes­ti­cles and the fal­lop­ian tubes to help match our repro­duc­tion to the amount of food avail­able. As the D level climbs in the fall, to 80 ng/ml, we make higher estro­gen and testos­terone lev­els that make us want to mate. Because our babies develop over 9 months, the baby that is con­ceived in Sep­tem­ber is born in June. This guar­an­tees that at birth the baby is in the sun mak­ing her own D hor­mone because there is no D in the breast milk. Low D sup­presses ovu­la­tion so that our babies will be born when mom has food. “Poly­cys­tic ovary” describes an ovary with many eggs that are all try­ing to mature at once. Because ovu­la­tion is inhib­ited by the low D, the ovaries are stuck at the stage of many eggs try­ing to mature and cysts develop, lead­ing to abdom­i­nal pain, often accom­pa­nied by weight gain and acne (the triad of symp­toms called poly­cys­tic ovar­ian syndrome). Endometrio­sis results from endome­trial tis­sue going back­ward up the fal­lop­ian tube into the abdomen instead of out the cervix, (the open­ing in the uterus), dur­ing men­stru­a­tion. Because the fal­lop­ian tube is open into the abdomen, the only thing that keeps the endome­trial tis­sue head­ing out the cervix are wave-like move­ments in the fal­lop­ian tube push­ing toward the uterus. There are vit­a­min D recep­tors in the fal­lop­ian tubes that influ­ence the propul­sive move­ments, pro­mot­ing or pre­vent­ing fer­til­iza­tion depend­ing on the D level. Also, once the endome­trial cells have arrived in the abdomen, where they don’t belong, the white blood cells are sup­posed to find and kill them. Because the low D also affects the func­tion of the white blood cells the proper elim­i­na­tion of the endome­trial tis­sue doesn’t occur and fixed implants of endome­trial tis­sue appear in the abdomen, caus­ing abdom­i­nal pain dur­ing menstruation. Women bear­ing babies are the ones who are most affected: The rea­son why thy­roid dis­ease, gall­blad­der dis­ease, B12 and iron defi­ciency, obe­sity and sleep dis­or­ders (and there­fore severe headaches) often occur in young, healthy women is because they’re the ones hav­ing the babies. Each baby sucks up mom’s vit­a­min D using it for devel­op­ment. Unfor­tu­nately, each pre­na­tal vit­a­min has only 400 IU of vit­a­min D, which is not nearly enough to pro­vide for mom and the devel­op­ing baby. When we all lived out­doors mom would get preg­nant again as soon as she made enough D to sleep nor­mally and get her body ready for the next baby. Now, each baby uses up mom’s D and if she’s not out in the sun enough after deliv­ery her D deficit is never cor­rected between preg­nan­cies. Each result­ing child is more D defi­cient and each baby sleeps worse than the last. Mom also sleeps badly, being more D defi­cient her­self with each baby. The chronic sleep dis­or­der over sev­eral years can result in post­par­tum depres­sion and occa­sion­ally psy­chosis; (abnor­mal thoughts and hal­lu­ci­na­tions). I believe that once the sleep is very, very abnor­mal, the “sleep switch” (which is designed to be sure that we never dream while we’re awake) may start to mal­func­tion, and dream-like expe­ri­ences (hal­lu­ci­na­tions) may start to leak into wak­ing life. Some com­monly used med­ica­tions pre­ventREM sleep: Unfor­tu­nately many of the com­monly used anti­de­pres­sants, though they keep the sero­tonin up dur­ing the day to make us hap­pier, also make the sero­tonin stay up inap­pro­pri­ately at night. High sero­tonin lev­els at night sup­press REM sleep, para­dox­i­cally pre­vent­ing the very phase of sleep that might give us back nor­mal pro­duc­tion of our own sero­tonin. Long term REM depri­va­tion is prob­a­bly the most com­mon cause of depres­sion. Over the last thirty years there has been a dra­matic increase in the inci­dence of depres­sion, sleep dis­or­ders and vit­a­min D defi­ciency in all of the devel­oped coun­tries of the world, I believe these three con­di­tions are linked. Vit­a­min D and aging: Even under per­fect cir­cum­stances, with per­fect sun expo­sure, we don’t live for­ever. Humans live about 90–100 years. Every decade our vit­a­min D pro­duc­tion (per hour of sun expo­sure) goes down. At age 70–75 the vit­a­min D pro­duc­tion on our skin goes so low that four com­plaints become com­mon in the elderly; “my bow­els don’t work”, “I’ve got rheuma­tism” (I wake up stiff and in pain), “I don’t sleep well”, and “my nose runs all the time.” When the sleep starts to fail we begin to get hyper­ten­sion, dia­betes, high cho­les­terol, heart dis­ease, stroke or can­cer and die 5–10 years later. There­fore our abil­ity to sleep nor­mally is linked to our life span. What should my vit­a­min D level be? How much would my body make nor­mally out in the sun? When we sit in the sum­mer sun, at noon, with chest, face, and arms exposed we make 10,000 IU of vit­a­min D. Whole body expo­sure pro­duces 20,000 IU in 2–4 hours. The rate of pro­duc­tion is depen­dant on the skin color. Darker skinned peo­ple make D more slowly for equal time spent in the sun. Because we don’t have fur or feath­ers cov­er­ing our skin, the melanin col­oration in the skin keeps us from mak­ing too much D. Lighter skinned humans began to appear in far north­ern and south­ern lat­i­tudes because their lighter skin color did not block the D pro­duc­tion. They were stronger and could repro­duce in lower sun envi­ron­ments where D was scarce. How­ever, those bright white or freck­led peo­ple have a dis­ad­van­tage when they move to a high sun envi­ron­ment, they don’t have the nat­ural melanin pro­tec­tion and they burn. When humans are adapted to their lat­i­tude with the “proper” col­oration, and their inter­nal D level is high enough, some of the pro-D on the skin is con­verted to D 1,25 OH, the active hor­mone which goes into the nuclei of the skin cells to repair the UVB induced DNA dam­age, thus help­ing to pre­vent skin can­cer under nor­mal circumstances. As most of us don’t receive “sun D” every day, our sup­ple­men­tary vit­a­min D require­ments are much higher than the FDA rec­om­mended 800 IUper day, and are prob­a­bly closer to 5,000–10,000IU per day just to stay the same. To sleep nor­mally the vit­a­min D blood level must be 60–80ng/ml. The vit­a­min D25OH that we mea­sure in the blood is “stor­age D”. We make the active chem­i­cal; D 1,25 OH every minute of the day, in each organ in rela­tion to its need. When your doc­tor mea­sures your D blood level it should be the D 25OH, not the D 1,25 OH. Why FDA rec­om­men­da­tions are so low: Chole­cal­cif­erol is a hor­mone not a vit­a­min. We would never dream of putting estro­gen or testos­terone or thy­roid hor­mone into the milk. Because it was incor­rectly called a “vit­a­min” the FDA has been put in the very dif­fi­cult posi­tion of mak­ing “rec­om­men­da­tions” for hun­dreds of thou­sands of peo­ple who have dif­fer­ent D lev­els from year to year depend­ing on their lifestyle, where they live and their skin color. The FDA knows that high vit­a­min D lev­els can cause med­ical prob­lems and death, they just don’t really know why. (I think it is because vit­a­min D makes the sleep just as abnor­mal when it goes over 80, as it does when it’s under 60, there­fore every­thing I have described above results from a high vit­a­min D just as eas­ily as from a low vit­a­min D). The FDAhas appro­pri­ately rec­om­mended a dose of vit­a­min D, 400–800 IU/day, that is unlikely to hurt any­one. This does not mean that 800 IU is what you need. Each per­son must find out what dose they need by mea­sur­ing their blood level. Every­one who takes this hor­mone in big­ger doses must fol­low their vit­a­min D blood level. Ask your doc­tor to mea­sure your vit­a­min D 25OH level. Most doc­tors do not know what the “nor­mal” D level really is, so ask for the num­ber, it should be between 60–80 ng/ml. Medicare will pay for vit­a­min D lev­els four times per year if a billing code of 268.9 (vit­a­min D defi­ciency) is used on the lab slip. If you don’t have insur­ance www.vitamindcouncil.org will do your level for $75.00. All your ques­tions about vit­a­min D are answered at www.vitamindcouncil.org. It is a site started in 2003 to teach you and me about this hor­mone. It has thou­sands of sci­en­tific ref­er­ences link­ing vit­a­min D defi­ciency to var­i­ous dis­eases, and teach­ing about how to use vit­a­min D safely and effectively. What is the right D hor­mone dose? For most peo­ple the daily sup­ple­men­tal D dose will be 1–5000 IU per day in sum­mer, 5–7,000 IUper day in win­ter, but if your level is 30 or below and it’s win­ter, I rec­om­mend that you take10–15,000 IU for 2–3 weeks to get your level back above 50 more rapidly. Then check your level again in 4 weeks to be sure it is above 60. Over1–2 years mea­sure your D lev­els every 6 to 12weeks and make sure that you are tak­ing enough to pro­vide a D level between 60–80 ng/ml all year long. Don’t take extra D when you’re using a tan­ning bed or out in the sun in the sum­mer, you’ve just made your daily sup­ply on your skin. Never take doses over 1000 IU/day with­out check­ing your lev­els regularly.

Spray chart

For info on the QD3 Spray and the rest of the Q Sprays check out my site at:  http://q4mentalhealth.myqxlife.com

Thank for reading, I know that was a long one  :)

Charm Brewer

Q Sciences IBO