There is a safe

 There is a safe, easy, natural way to cure mood disorders and reclaim a life of health and happiness without spending a fortune or relying on dangerous (and often ineffective) drugs.


If You or Someone You Love
 Suffers From Depression, Anxiety,
Insomnia, Attention Deficit or Any “Mood Disorder,”
This May Be The Most Important Letter
You’ll Ever Read

From: Dr. Dana Myatt
                                
Chief Medical Officer, Dr. Myatt’s Wellness Club
                        To: 
People Suffering from Mood Disorders

 

                        Dear Friend:

                        There is a “dirty little secret” known in many medical and scientific circles about “mood disorders” (depression, anxiety, etc.) …
                         a secret you will probably never hear from your doctor …and the Big Drug Companies want it that way.

                        This “dirty little secret” is the reason that 72% of people diagnosed with a mood disorder don’t feel better
                        regardless of what “head med” (drug) they take, and why even those who do feel somewhat better
                        with drugs often find that the “improvement” stops working after a while or still doesn’t make them feel
                        really good. If you knew the “dirty little secret” that is known to medicine’s “inner circle,” you would find yourself able to:
                       

                                    * not just feel “better,” but truly goodagain …

                                    * end fatigue, lethargy, anxiety and hopelessness in a few days, sometimes overnight …

                                    * skyrocket your energy levels without stimulants …

                                    * sleep like a baby all night long and wake rested and refreshed….

                                    * say “goodbye” to depression and anxiety without drugs….

                                    * reclaim your happy, energetic self in record time with NO dangerous drug side-effects

 

                        The best part is, you won’t need to take costly “head meds” or stimulants indefinitely
                        (which don’t work well anyway), pay thousands of dollars for often-ineffective counseling,
                        and still spend the rest of your life feeling only “half alive” because of a mood disorder. All you need to
                        know is the “dirty little secret” that has been kept behind closed doors… until now.


3 Lies Your Doctor Probably Told You About Mood Disorders
(
and he doesn’t even know they’re lies…)

Lie # 1: Mood disorders are caused by a serotonin deficiency. In some cases, this is true. (Note: did your doctor ever actually TEST your serotonin levels to verify this? Answer: Almost certainly “NO”). Even if serotonin deficiency is your problem, as it is for some people with mood disorders, conventional drugs like Prozac and Zoloft only block the re-uptake of this neurotransmitter, giving your body the false impression that more serotonin is available. Treating “serotonin deficiency” without a test is not only a “shot-in-the-dark,” but the treatment itself is a “patch-job,” instead of a “fix.” Selective serotonin re-uptake inhibitors (SSRI’s) do not increase serotonin levels, and the artificial blocking of re-uptake eventually depletes serotonin levels even more.

Lie # 2:  Drugs are the best treatment for mood disorders. Come on. Do you really think depression is caused by a Prozac deficiency? Or that anxiety is caused by a Trazadone deficiency? Changes in brain chemicals (called Neuro-Transmitters) cause the symptoms we collectively call “mood disorders.” These changes in brain chemistry can be identified and corrected by natural means, restoring them to normal levels.
                       
Lie # 3:  There is no way to test Neurotransmitter levels. Actually, NeuroTransmitter Testing has been around for years. Your doctor could test and know exactly what “head hormones” (neurotransmitters) you are low or high in and make specific corrections. But keep reading and you’ll find out why he/she probably doesn’t even know about this test, and if they do, why they can’t (won’t) order it for you…..

___________________________________________________

The Real Cause of Mood Disorders That
Big Drug Companies Hope You Never Find Out

 

                        Doctors know that brain chemicals — called Neuro-Transmitters, or “NT’s” for short—- control everything from mood and sleep to food cravings. Most people have heard of at least one of these Neurotransmitters,  serotonin, but there are other major NT’s including epinephrine (adrenaline),norepinephrine, dopamine,                                     GABA, PEA and histamine. Together, these major Neuro-Transmitters control mood, libido, food cravings, sleep patterns and energy levels to name only a few. When any one of these NT’s are out of balance (as they are in an estimated 85% of the population with mood disorders), the implications can be enormous:

                                   

                             Serotonin:
                                           Too little can cause depression, anxiety, sleep disturbances, uncontrolled appetite, migraine headaches, obsessive/compulsive disorders and PMS complaints.

                                           Too much serotonin is rare and is caused by excess drugs or other serotonin-increasing treatments. Serotonin overdose can be life-threatening.

 

                             Epinephrine (adrenaline): too much can causes sleep disturbances, anxiety and ADHD. Too little causes fatigue,  depression, lack of focus and difficulty losing weight.       

                             Norepinephrine (NE): Too much causes anxiousness, stress, hyperactivity and high blood pressure. Too little causes fatigue, lack of focus and difficulty losing weight.

                             Dopamine: responsible for feelings of pleasure and satisfaction. Low levels play a role in Parkinson’s  disease and also in addictions and food cravings.  High dopamine is seen in people with autism,  attention disorders and GI disturbances. 

                             GABA

 

                             glutamate is the major excitatory neuro Transmitter in the brain. Excess glutamate is associated with neurological diseases such as Huntington’s disease, parkinson’s disease, Alzheimer’s, vascular dementia, ALS, Tourette’s syndrome and Korsakoff syndrome. While excess glutamate alone probably does not cause these diseases, it is felt that high levels of glutamate may be toxic to nerve cells and indicate toxicity elsewhere in the body.                                                  

                       

                        Doctors use various “head meds” (like Prozac or Zoloft) to increase serotonin’s effects. (Notice I said effects; these drugs do not increase actual serotonin levels). Sometimes these drugs help depression, but often not. That is because the other major Neurotransmitters’s — epi, NE, dopamine, GABA and glutamate — are also intimately involved in mood and “feel good” control. “Tinkering” with only one neurotransmitter — serotonin — may not help much if any of the other five major neurotransmitters are out of balance. In many people with anxiety, depression or other mood disorder, serotonin levels are not the only problem or not even the problem at all. Many cases of mood disorder havenothing to do with serotonin but instead involve one or more of the other major neurotransmitters.

So why doesn’t “Big Medicine” and “Big Pharma” want you to know that other neurotransmitter imbalances may be the cause of your depression? Because NT imbalances can be corrected with a few simple diet changes and some inexpensive over-the-counter supplements. Drug companies don’t have drugs to effectively correct other neurotransmitter except serotonin and norepinephrine. Depression medications like prozac, zoloft, XXX and XXXX are BIG BUSINESS, raking in $XXXXX of dollars for major drug companies each year. If even a small percentage of the 19 million depressed Americans discovered how to correct their depression without drugs, Big Pharma income from these drugs could drop precipitously. Or imagine if XXXX million children and adults no longer needed Ritalin and other stimulants! Believe me, the Big Drug Companies will do everything they can to make sure this doesn’t happen — including convincing your doctor and you that your only hope for treating a mood disorder is dangerous drugs. Even more appalling is that these drugs effects only ONE, or at most TWO major neurotransmitters — even if you have never had your neurotransmitters levels tested!

__________________________________________

Your Secret Weapon for Conquering Mood Disorders

                        Balancing the body’s six major neurotransmitters —  serotonin, epinephrine, norepinephrine, dopamine, GABA and glutamate — is the secret to feeling good and getting out from under the dark cloud of depression, anxiety, insomnia, attention deficit or any other mood disorder you may suffer from. Other “side-effects” of balanced NT’s (as if being free from depression or anxiety weren’t enough!) include sound sleep, improved libido and energy, normal appetite and better fat-burning. If you are over or under weight, body weight tends to normalize because mood disorders are a common cause of over and under-eating.

                        As you’ll learn, there are simple, natural ways to increase or decrease neurotransmitters. For example, two amino acids (both readily available in any health food) provide the raw materials that the body uses to produce epinephrine and norepinephrine. By supplementing these amino acids, a person who is low in epinephrine (adrenaline) or norepinephrine can improve their neurotransmitters levels without drugs, just by taking these amino acids between meals. By using “precursors” (raw materials that the body uses to make NT’s), the resulting increased NT levels are a true “fix,” not just a “band aid.”

                        Normal neurotransmitter levels are the key to a happy, energetic, symptom-free life. The correction for imbalanced neurotransmitters involves a few simple diet changes and some inexpensive, easily obtainable nutritional supplements. So what is holding you back? Obviously, you need to know which neurotransmitters are out of balance before you can begin an NT-improvement program. As you can see from the list of NT’s above, excesses cause just as many problems as deficiencies. The secret to normal neurotransmitter balance begins with knowing your neurotransmitter levels.
________________________________________
                                   
The Medical Test
That Can Save Your Life

______________________________________

 

Perhaps You’re Wondering,
“Why Didn’t My Doctor Order This Test…?”

Your doctor did not order a NeuroTransmitter test fortwo important reasons:

First, because he or she doesn’t know about it!Big Drug Companies aren’t “pushing” these tests yet because they don’t have drugs to address every neurotransmitter imbalance. Would you want to continue taking a serotonin-effecting drug, for example, if you found out you were low in epinephrine instead? And what about your doctor? The pharmaceutical industry is responsible for most of a doctor’s training, including the medical school curriculums. American medical schools are still marching to the Big Pharma tune. And Big Pharma isn’t ready for you or your doctor to know about simple ways to correct Neurotransmitter imbalances, especially when “head meds” are such Big Business.

Second (and this one may shock you), a doctor can besued by either your insurance company OR the federal government for ordering a “non standard” medical test. You read that right. The Big Drug Companies have such a stronghold on doctors and the government that a doctor can only order those tests that the drug companies “approve of.” Big Pharma isn’t going to let the cat out of the bag about Neurotransmitter Testing until they have drugs to sell you to “correct” any NT imbalance that testing discovers. And while norepinephrine drugs have just recently been introduced (which means we are the “guinea pigs for testing their safety), there are no other “head meds” on the horizon. That means that you’ll be waiting for years— perhaps even a decade or more—before your doctor will know about this test and  order it for you.

As I showed you in the first half of this report, your doctor is telling you some potentially deadly lies-and he doesn’t even know it.

But it isn’t his fault. He simply never learned in medical school or in mainstream journals about the safe, natural miracle-cures that are all around us, but known only to an unorthodox, yet dedicated few. It’s a shame, but the modern medical establishment is so dominated by the pill and scalpel that these un-patentable (read: inexpensive and difficult to regulate) cures get swept under the rug by our Big Pharma-friendly government…

 

________________________________________


Ignorance Isn’t Bliss, It’s Blistered

As we discussed earlier in this report, your doctor is telling you some potentially deadly lies-and he doesn’t even know it.

But it isn’t his fault. He simply never learned in medical school or in mainstream journals about the safe, natural miracle-cures that are all around us, but known only to an unorthodox, yet dedicated few. It’s a shame, but the modern medical establishment is so dominated by the pill and scalpel that these un-patentable (read: inexpensive and difficult to regulate) cures get swept under the rug by our Big Pharma-friendly government…

_________________________

 

3 Reasons Why I Know You’ll Find Your
Neurotransmitter Improvement Program So Valuable

1.) Knowledge is Power. Whether you choose conventional drugs, natural (corrective) remedies or a combination of both, at least you will know exactly what neurotransmitters need to be normalized, instead of just going along with the conventional medical “guess” and treating only serotonin levels.

2.) You’ll know your Options.  Your follow-up report will detail which drugs, supplements, diet and lifestyle changes are available to correct your particular neurotransmitter imbalances.

3.) You’ll discover proven ways to live a healthier, happier life.  When you balance your brain chemistry through corrective measures, you’ll not only feel happier, you’ll be genuinely healthier.

_______________________________________________

Lift DEPRESSION Overnight
By Pressing Your “Happy Buttons”

_______________________________________________________________

What Patients Have To Say
About the Neurotransmitter Improvement Program….
(testimonials here)

“You Have Make A Huge Difference…”
“I feel like I have my life back. I really didn’t realize how depressed I was. Things seemed  better after I started taking Zoloft, but it was only after we discovered that I was low in epinephrine and norepinephrine, and made some changes, that I could tell the difference beween ‘just getting by’ and really living. It’s hard for me to find the words to express how greatful I am for this test and your recommendations.” John Abrams, Phoenix, Arizona

“I Have Already Experienced Great Changes In Myself Because Of The Principle #1 Exercise…”
” I started taking the recommended supplements just two days ago and I can already feel a difference. I slept better last night than I have in years. I really do believe with such fast improvement in my sleep that help is on the way…” Katherine K., Poduk MI

“Your NT Program Recommendations Are Easy To Follow…”
“I learned through NT testing that I had three neurotransmitter imbalances (none of which was serotonin, which explains why Prozac wasn’t helping me). But I was afraid that “natural treatments” would involve some strict diet and exercise plan and eating foods I don’t like, like tofu. I was pleasantly surprised to find that Dr. Myatt’s recommendations were simple and easy to follow. Even better, I have experienced dramatic results in only two weeks. THANK YOU SO MUCH DR. MYATT!”

“TheNIP Program Has Empowered Me To Take Control Of My Life…”

“NIP Has Truly Changed My Life…”

” TheNT Test and Program Have Accomplished in Three Weeks what Drugs and Counselling Failed to Produce in Three Years…”

_____________________________________________________

Your Personal Neurotransmitter Improvement Plan (NIP) will be:

Simple — That’s because simple is the thing that works the best.

Fast Results — When you invest in this course, or in anything, you are doing so because you want results sooner rather than later.owever, you have to be open to fast results. This sounds crazy, but if you believe in the saying “anything worth having is worth waiting for” than you are going to live a life waiting. Let’s start getting results right now – fast, immediate – with these 11 Principles.

Real Life
— Principles from the real world always work better (or else they would not be principles) than the “should be’s” some people try to get you to believe.

Realistic, A Game Plan — Do you agree that information without a plan that shows you how to use it is worthless information. That means even poor information, if it at least comes with a game plan, will benefit you.

So imagine what superior information, with a specific, easy to follow game plan like the 11 Principles course is worth to you… Not only do you learn each of the 11 Principles, you also see how other people like yourself have used them. And most importantly, you are given an easy to follow game plan to quickly and simply put each Principle into use for yourself.

____________________________

 

 

                       

 

Don’t just swallow a pill (and the marketing hype that goes with it) and carry on with business as usual. True neurotransmitter-balancing treatment is worth its weight in gold -and far outweighs the use of tranquilizers, anti-depressants, sleeping pills and other synthetic mood-altering drugs. So stop the drain on your health and feel like yourself again.

                             ___________________________

                        Drug-free treatments work like Prozac without dangerous side effects. Prozac and other antidepressants work by boosting your levels of the mood-enhancing chemical serotonin. Yet researchers have now discovered a technique that does the very same thing — without drugs!
_________________________

Believe me, this isnot “pop medicine.” Just the opposite. These unpublicized techniques were revealed to our editors by a team of over 250 leading physicians and scientists, then carefully double-checked against the latest research. You won’t find them in the popular press — and unlike the fluff printed there, these things work.

_______________________________________

We are supposed to have freedom of speech in this country, but even many courageous alternative medical doctors don’t dare dare discussnew medicines or testsuntil they are “approved” by conventional medicine.Funny thing is, many of these leading-edge discoveries will in fact become “accepted”—- just as soon as Big Pharma figures out how to make a profit from them.

___________________________________________

Neurotransmitters are naturally occurring chemicals within the brain that relay signals between the nerve cells and are required for proper brain and body function. A proper balance of neurotransmitter levels helps achieve optimal health.

_________________________________

Prescribing drugs based on opinions, theories and guesswork is like driving blindfolded. Without actual testing, you won’t discover your real Neurotransmitter imbalances except by accident.

Even “medicalexperts” find it hard to predict how patients will respond to a Neurotransmitter-effecting drug like Prozac or Zoloft. What’s more…

Testing often proves “expert opinions” dead wrong — and can skyrocket response and profits through the roof!

Simple diet, lifestyle and supplement changes can dramatically improve your neurotransmitter balance and hence, your mood and happiness level. But unless and until you test, you’ll never know what those needed changes are.

 

_____________________________________________________________

____________________________________________________________________________________

Lift depression, Balance Your NT’s and see:

Better Results In Your BUSINESS

Better Results In Your HEALTH

Better Results In Your JOB

Better Results In Your Relationships

______________________________________________

How Much Is The Neurotransmitter Improvement Program?

The total value of the Neurotransmitter Test plus your personalized follow-up report —what I call the Neurotransmitter Improvement Program — is $794. And that would still be an incredible bargain based on the results it can bring you. But because I want to make this program available to as many people as possible before the “window of opportunity” closes, I’m going to make you an incredible offer.

Can you even put a price tag on a healthy, happy life?

How much would you give to wake up tomorrow morning living that dream life you gaze at every day in your head?

However, I want to get this life-changing information into everybody’s hand at a very reasonable price. And since this test is not yet “recognized” by conventional medical insurance (and won’t be until Big Pharma figures out how to get into the act), you’ll be paying out-of-pocket. Instead of the usual $794cost of theNeurotransmitter Test plus a New Patient Consult and follow-up report from me, I have chosen to make the entire program available for the cost of the NT test alone, $297.

Cost of NIP Program including NT test and Personalized Report: $297
Cost of feeling healthy, happy and energetic again: priceless

—————————————————————–

Money-Back Guarantee

Perhaps you are concerned about the test results. What if your test results say that all of your neurotransmittrs are completely normal? Personally, I’ve never seen completely normal test results in a person suffering from depression, but I suppose it could happen. Now, a test result is a test result. The lab isn’t going to give us our money back if we don’t like the test results, any more than you’d get your money back for any other medical test result that you didn’t like. (Did you get your money back when you didn’t like hearing that you had high cholesterol? Or high blood sugar?) But I am SO CONFIDENT that if you suffer from depression, anxiety, ADD/ADHD or other any other mood disorder that  neurotransmitter imbalances will be discovered which will lead you to a better life, that I will personally make this guarantee:

If your NeuroTransmitter Profile results come back completely normal, I will personally return your money— you won’t even have to ask for it back. Not only that, but you can keep your bonuses. Even in the presence of normal test results (again, I’d be quite surprised), your personal report will contain suggestions for increasing your health and happiness levels.

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P.S. If you recognize the enormous value of this program, please order your Neuro Improvment Program today. I don’t know how long I can continue to offer The Neurotransmitter Test, which requires a “doctor’s order.” You see, I’ll have a lot of people “gunning” for me when they find out what I am offering, and I could be barred at any moment from making this life-changing test and report available. The drug companies won’t like it because hey don’t want you to find out that you may have a neurotransmitter imbalance that is correctable without one of their drugs. Other doctors who use this test won’t like it, because it may deprive them of a new patient visit and numerous follow-up visits. (Remember, the test can only be ordered by a doctor, so ordinarily you’d have to visit a physician who would order the test for you). Even the labs who perform the tests might get a little “testy” when they learn that I am offering this test to people that I haven’t seen in person. But until someone cuts me off, I’ll do my best to make this test available. I believe it’s that important. Because I have no idea how long I can offer it, please don’t delay. If you return to this page and it’s gone from the Internet, it will mean that this service is no longer available to anyone except a private practice patient of mine.
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Three Free Bonuses: Yours to Keep no Matter What

1.) The Body/Mind Connection DVD.

2.) FREE report: 29 simple, natural strategies to lift depression and live a life of joy.

3.)  [JV partner bonus here?]
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REFERENCES:

 

Recommended Reading

Commonsense Rebellion: Taking Back Your Life from Drugs, Shrinks, Corporations, and a World Gone Crazy (Paperback) by Bruce E. Levine, pHD. Continuum Press, 2006.

 

 

                       
                       

 

                       

                       


 

 

 

Dr. Dana Myatt’s Wellness Club

Dr. Dana Myatt is here to help you.Dr. Myatt’s Curriculum Vitae and Credentials

Current Positions and Professional Activities

  • Physician: Worldwide holistic medical consulting; Anti-Aging and Longevity Medicine / Natural and Holistic Health Care (sub-specialties include: bio-identical hormone replacement; thyroid and adrenal balancing; weight loss; fertility; male hormone balance; natural diabetes correction)
  • Chief Medical Officer, Dr. Myatt’s Wellness Club, Snowflake, Arizona
  • Chief Medical Officer / Formulator, Dr. Myatt Nutritionals, Snowflake, AZ
  • Medical Director, Fertility Restore, Snowflake AZ and Long Island, NY
  • Author: Four books including the forthcoming The Keto Zone Diet
  • Public Speaker / Medical Educator

Previous Medical Experience / Positions

  • A.R.E. Medical Clinic, Phoenix, AZ. Director of Medical Residencies / Admissions Evaluation Physician – Neurological Improvement Program
  • Scottsdale Holistic Medical Group, Scottsdale, AZ., Staff physician; Director of the Health Optimization Program
  • Private Practice – Virginia Beach, Va.

Professional Memberships and Affiliations

  • Arizona Naturopathic Medical Association (AzNMA)
  • American Association of Naturopathic Physicians (AANP)
  • American Society for Reproductive Medicine (ASRM)
    * Reproductive Immunology
    * Fertility Preservation
    * Androgen Excess
  • American Academy of Anti-Aging Medicine (A4M)
  • The Institute for Integrative Medicine (IFIM)
  • Naturopaths International

Medical Education / Degreesclick to show/hide

Graduate:

  • 1989 – National College of Naturopathic Medicine (N.C.N.M.), Doctor of Naturopathic Medicine

Undergraduate:

  • 1983 – University of Nevada, Reno, Bachelor of Science in Biology with Medical Science Minor

Pre-Medical:

  • 1978-79: Neurological Research Assistant to Dr. Robert William, Chief of Neurosurgery, Sunrise Hospital, Las Vegas, NV

Medical Licensesclick to show/hide

  • Medical License: Oregon 1989
  • Medical License: Arizona 1990
  • Drug Enforcement Agency: 2000

Medical Certificationsclick to show/hide

  • Advanced HAZMAT Life Support – Instructor and Certified Provider, University of Arizona College of Medicine
  • Licensed Massage Therapist (LMT) – Oregon, 1988
  • Certified Health Counselor – Human Services Institute, Phoenix, AZ.

Continuing Medical Educationclick to show/hide

2012

  • Fall Managed Care Forum 2012. 6 hours AMA PRA Category 1 Credit
  • Supply-Side West, “How to Look at a Research Study under a Microscope.” 3 courses, non-CME Credit
  • Mayo Clinic: Acute and Chronic Leukemias 2012: A Case Based Discussion. 7 AOA PRA Category 2-A Credits.
  • A4M: Nutritional Therapy in a Medical Practice (Dr. Wright and Dr. Gaby) – 23 AMA PRA Category 1 Credit
  • Nutritional Medicine Update: Review and Analysis of Important New Research from a Trusted Expert (Alan Gaby, M.D.) – 2 hours CME
  • Medscape CME – 15 AMA PRA Category 1 Credit

2011

  • AzNMA Fall Conference – Thyroid and Adrenal Function and Treatment – 13.5 hours
    Dr. Myatt was also a presenter at this conference, speaking on “Beyond Broda Barnes and Basal Body Temperature: Diagnosis and Treatment of Hypothyroid Conditions Using Laboratory and Physical Methods.”
  • Medscape CME – 14 AMA PRA Category 1 Credit

2010

  • 18th Annual World Congress on Anti-Aging Medicine and Biomedical Technologies (21 CME’s)
    Dr. Myatt was also a presenter at this conference, speaking on “Dietary Ketosis in the Treatment of Overweight, Obesity and Metabolic Syndrome”
  • IFIM – First Annual Integrative Medical Conference – 16.5 AMA PRA Category 1 Credit
  • Medscape CME – 6.5 AMA PRA Category 1 Credit

2009

  • Naturopathis International First Aid Training – 14 hours AzNMA
  • Physical Manipulation of the Cervial Spine – 8 hours AzNMA
  • 17th Annual World Congress on Anti-Aging and Regenerative Biomedical Technologies – 28.5 AMA PRA Category 1 Credit
  • NorthWest Herb Fest – 15.5 hours AzNMA
  • Medscape CME – 6.25 AMA PRA Category 1 Credit

2008

  • Bio-Identical Hormone Replacement Therapy /Treating Adult Hormone Deficiencies — Advanced Course – 23 hours CNDA
  • High Performance Weight Loss and Associated Neurotransmitter Diseases – 16 AMA PRA Category 1 Credit
  • Medscape CME – 23 AMA PRA Category 1 Credit

2007

  • Recent Advances in the Use of Iodine in Medical Practice – 14.5 hours AMA PRA Category 1 Credit
  • Medscape CME – 24 AMA PRA Category 1 Credit

2006

  • Genomics in Everyday Medical Practice – Mayo Clinic, Scottsdale – 14 AMA PRA Category 1 Credit
  • AzNMA Semi-Annual Southwest Convention – 26 hours AzNMA
  • Medscape CME – 23 AMA PRA Category 1 Credit

2005

  • Advanced HAZMAT Life Support Provider and Instructor Program – Univ. of Arizona College of Medicine – 23 AMA PRA Category 1 Credit
  • Medscape CME – 31.25 AMA PRA Category 1 Credit

2004

  • Cardiovascular Pharmacology -15 hours AzNMA
  • Rheumatology, Gastroenterology, Diabetes, Osteoporosis, Thyroid, Asthma, COPD, Allergy, Hormones and Dermatology – 15 hours AzNMA
  • Medscape CME – 7.75 AMA PRA Category 1 Credit

2003

  • Introduction to Pharmacodynamics/Kinetics – Drug Interactions – 15 hours AzNMA
  • IV Therapy Protocols – 15 hours AzNMA
  • Medscape CME – 21.25 AMA PRA Category 1 Credit

Speakingclick to show/hide

  • Beyond Broda Barnes and Basal Body Temperature: Diagnosis and Treatment of Hypothyroid Conditions Using Laboratory and Physical Methods.
  • Dietary Ketosis in the Treatment of Overweight, Obesity and Metabolic Syndrome
  • Dietary Ketosis in the Treatment of Cancer
  • The Urgent Care Herbalist Part I & II
  • Botanical and Nutritional Treatment of Malignancy
  • Black Salve Intensive
  • Laboratory Evaluation of Immune Dysfunction
  • Botanical and Nutritional Considerations in the Treatment of Lymphoma
  • Treatment of Prostate Cancer: Botanical and Nutritional Considerations
  • Detoxification with Botanicals: A “Systems” Approach
  • Skin Rejuvenation with Natural Cosmetics
  • Botanical Considerations in the Systemic Treatment of Cancer
  • Botanical Treatment of Stroke, Thrombosis and Phlebitis
  • A Traditional Appraoch to the Treatment of Modern Illness
  • Protocol 2000: Longevity and Rejuvenation with Botanicals
  • Prescription and O.T.C. Drugs and Herbal Alternatives
  • Mood and Attentional Deficit Disorder in Children: Alternatives to Ritalin and Prozac
  • Botanical Treatment of Malignant Melanoma: “The Black Salve”
  • Herbs for Weight Loss
  • Herbal Treatment of Malignant Melanoma
  • Parasites: Diagnosis and Treatment
  • Understanding and Using the Toxic Botanicals
  • Essential Oils for Clinicians Part I & II
  • Empowering Yourself to Heal
  • The Body/Mind Connection
  • Remembering Who You Are

Teaching Experienceclick to show/hide

  • Atlantic University – Associate Professor of Holistic Health
  • Reilly School of Massotherapy – Anatomy and Physiology Instructor
  • Clark Country Community College, Las Vegas, NV. Anatomy and Physiology Instructor

Books and Publicationsclick to show/hide

Videoclick to show/hide

Honors and Awardsclick to show/hide

  • City of Portland, Long-term Care Ombudsman – Outstanding Service to Seniors
  • National College of Naturopathic Medicine – Board of Directors Award of Appreciation

Bio-Identical Hormone Therapy

Bio-identical (Natural) Hormone Replacement Therapy
and Other Natural Hormone-Balancing Therapies

Which One is Right for You?

Index:

Are Your Symptoms Cause by Low or Imbalanced Hormones?

What is Bio-identical Hormone Replacement Therapy (bHRT)?

What are the advantages of bHRT?

Delivery System: Oral Versus Transdermal Hormones

How Best to Address Your Menopausal Symptoms and Concerns?

Dr. Myatt’s “Hormone Balance” Programs: Which One is Right for You?

Are Your Symptoms Caused by Low or Imbalanced Hormones?

Women and men both go through “the climacteric,” a period in mid-life when sex hormone production declines.

In women, this change is called “menopause.” In men, the change is often referred to as “andropause.” Many symptoms of the climacteric are similar in men and women.

In women, peri-menopause (“around the time of menopause”) symptoms can include mood swings, weight gain, fatigue, hot flashes, breast tenderness, vaginal dryness, decreased libido (sex drive), urinary leakage or urgency and sleep difficulties. Menstrual periods may becomes less frequent, irregular and farther apart OR they can become heavier and more frequent. Peri-menopause usually begins in a woman’s 40’s but can start as early as the 30’s or as late as the 50’s.

Menopause symptoms in women are similar to peri-menopause symptoms except that menstrual periods cease. Headaches, heart palpitations, cognitive decline and difficulty sleeping may also occur. Bone mineral loss is often accelerated during this time, leading to osteoporosis.

Andropause symptoms in men can include include night sweats, low libido (sex drive), weight gain, depression, anxiety, hot flashes, gynecomastia (enlarged male breasts), fatigue, irritability, and weight gain. Other male climacteric symptoms include erectile dysfunction, loss of stamina and lean muscle mass, cognitive decline and decreased bone mineral density. Men with lower testosterone have a higher risk of coronary artery disease. (1-4)

The change in men is more gradual than in women and symptoms are often attributed to “natural aging” instead of hormone decline.

What is Bio-identical Hormone Replacement Therapy (bHRT)?

Bio-identical Hormone Replacement Therapy (bHRT) is a way to resolve symptoms and/or restore sex hormones to more youthful levels using hormones that are identical to those produced by the human body. Bio-identical hormone replacement therapy (bHRT) differs from convention HRT (cHRT) which uses horse estrogens (Premarin = Pregnant Mares Urine), synthetic and semi-synthetic hormones that are different from human hormones.

Proponents of bHRT believe that many of the unwanted side effects of conventional HRT are due to the “foreignness” of the molecules, not to hormone replacement therapy itself. This may make bHRT a safer form of hormone replacement therapy. (5-10)

How is Bio-Identical HRT Different from Conventional HRT?

Bio-identical hormone replacement is different from conventional HRT in the following ways.

  1. “Identical to human” hormones are used in bHRT. Conventional HRT typically uses horse hormones and synthetic and semi-synthetic hormones. These hormones are not the same molecules as those produced by the human body.It should be noted that there are bio-identical FDA approved hormones available by prescription. Not all “bio-identical” hormones need to be “compounded,” or made up individually by a compounding pharmacist.
  2. Based on Testing. bHRT is prescribed based on individual hormone test results. Conventional HRT does not use testing but bases treatment on improvement of symptoms.
  3. “Pulsed dosing” is often used in bHRT to duplicate the natural rhythm of hormone production and release. Some studies have shown this pattern of use to be safer and just as effective as continuous HRT. (11-12) Conventional HRT typically uses continuous doses of hormones. Continuous doses are associated with higher risk of breast cancer in some studies. (13)

What are the advantages of bHRT?

Is bHRT Safer than conventional HRT?

Conventional hormone replacement therapy, especially in women, is associated with a number of increased health risks including heart disease, stroke, breast cancer, deep vein thrombosis, gallbladder disease and acid reflux. (14-20) Conventional HRT decreases the risk of osteoporosis and can alleviate some symptoms of menopause including hot flashes and vaginal dryness (21-22) but many experts do not believe these improvements justify the increased risks.

Proponents of bio-identical hormone replacement therapy believe that bHRT is safer than conventional hormone therapy and some studies have shown this. (5-10) However, the number of studies done with bHRT is small compared to the studies done with conventional HRT. Large-scale studies of safety and efficacy of bHRT are lacking.

In spite of a small number of studies confirming safety and efficacy, the case for bio-identical hormones also makes sense in theory. Consider these facts:

Conventional hormone replacement therapy typically employs estrogens from pregnant mare’s urine. Horse hormones are significantly different than human hormones. Conventional hormone replacement also typically uses synthetic progesterone. The difference in synthetic and bio-identical progesterone is  significant. It is therefore believed that most if not all of the negative side effects of conventional hormone replacement is due to their “foreign to humans” molecular structure, not to hormone replacement itself. Some studies on bio-identical versus non-bio-identical progesterone confirm that there is a different effect in humans with natural progesterone appearing to have less risk of associated cancers. (5-10)

Further, conventional hormone replacement is almost always prescribed as a “one-size-fits-all” recommendation without the use of any laboratory testing to verify hormone levels. Practitioners of bio-identical hormone replacement typically start with blood, saliva or urine hormone testing and customize hormone prescriptions based on an individual’s unique requirements. Testing can help guide the prescription and prevent levels of hormones from being excessive.

Finally, risks associated with hormone therapy can be monitored, but this is rarely if ever done in conventional hormone prescribing. However, risks such as total hormone levels, ratios of hormones to each other and hormone metabolites can be potent predictors of heart disease and cancer risks. Even without hormone replacement therapy, these risk factors may be worth monitoring in all middle-aged men and women.

To answer the question of safety, there are theoretical reasons to believe that bio-identical HRT should be safer than conventional HRTand some actual studies show better safety.

Is bHRT Effective?

Studies have verified the effectiveness of bHRT for relieving many of the symptoms of menopause. (7-9, 23-24)

My personal clinical experience over the past 23 years is that bHRT can achieve every positive effect that conventional HRT achieves with less risk of negative side effects. Because I monitor risk factors, I have also seen reductions in cardiac and cancer risk markers and improvements in bone mineral density.

Is bHRT Proven?

Studies have demonstrated the effectiveness of bio-identical hormone replacement therapy. (7-9, 23-28)

Anti-Aging Claims for bHRT

Proponents of bHRT claim that keeping hormones at “youthful” levels can extend life expectancy and help delay the effects of aging. These claims have been popularized by public figures like Suzanne Somers in her book “The Sexy Years.” In spite of these claims, there is no proof that continued use of sex hormones, especially estrogen and progesterone in women, have-extending properties. There IS evidence that DHEA in both men and women (25-28) and testosterone in men (29-33) may have a positive influence on health, longevity and hormone balance.

While claims of living better and longer with bHRT are numerous, proof is lacking. This leaves bHRT and its anti-aging effects in the realm of theory at this point.

Delivery System: Oral Versus Transdermal Hormones

In addition to the “form” (natural or synthetic) of hormone, the method of administration has been shown to make a significant difference in safety and efficacy.

Orally administered hormones, especially estrogens, can increase risk of blood clots and deep vein thrombosis, increase hs-CRP (a marker of inflammation), decrease free testosterone and thyroid hormone and increase cortisol.(34) Oral estrogen is also associated with an increased risk of gallbladder disease and acid reflux. (15,18)

Many hormones used transdermally — applied to the skin or mucous membranes — do not appear to have these unwanted effects. (35) Therefore, when considering bHRT, the form that it is used in is also of importance.

How Best to Address Your Menopausal Symptoms and Concerns?

Symptoms of peri-menopause and menopause in women and andropause in men are a sign from the body that something is “off kilter.” For example, hot flashes in women correspond to an increase in oxidative stress and decreased nitric oxide levels (NO), both risk factors for cardiovascular disease. (36-37)

These symptoms and resulting negative physical changes are not an inevitable part of aging and should not be ignored. They can be addressed and improved through a variety of means, including but not limited to bio-identical hormone replacement therapy.

Diet changes, exercise and personal health practices can all help to improve symptoms of menopause and andropause. (38-39) There are nutritional and herbal supplements are proven to help correct menopause and andropause symptoms. (40-42)  Bioidentical hormone replacement is one way to address declining hormone levels, but it is not the only way.

The decision to use bHRT is a personal one that should be made in conjunction with an holistic physician. Your degree of symptoms, personal thoughts about bHRT, willingness to make other lifestyle changes and use nutritional and herbal supplements should all factor into the “decision equation.” Here are some additional factors to consider when making this decision.

Possible “Pro’s” of bHRT

  1. Faster. Herbs and other factors can help balance hormones, but the effects of bHRT might be more dramatic and faster. (NOTE: I cannot find scientific studies to support this; it is my clinical observation — Dr. Myatt)
  2. Easier. Taking an Rx. may be easier than making lifestyle changes, although any good holistic physician should recommend positive lifestyle changes as part of an overall health program.
  3. Safer. Some studies point to the improved safety of bHRT over conventional HRT. (14-20)
  4. Better hormone balance. Some hormones such as DHEA and testosterone have independent health benefits. (25-33, 43) These hormones are typically not used in conventional HRT but may be prescribed by a physician who uses bHRT.

Possible “Cons” of bHRT

  1. Cost. bHRT is not necessarily expensive and can be as little as $30/month depending on what hormones are needed. However, an Rx. will represent an ongoing expense. Most practitioners prescribing bHRT require initial hormone testing (to customize your Rx.) and follow-up testing to ensure that your hormones are at optimal (safe and effective) levels. Testing plus the Rx. itself will be an ongoing expense.
  2. Safety. Although bHRT appears safer than conventional HRT, there is some evidence that no type of hormone replacement in women has been proven to be “protective” or safer than natural menopause.

Alternatives to bHRT

Hormone Testing: Saliva vs. Blood vs. Urine

Conventional hormone replacement does not use testing. The recommended “end point” (goal of treatment) is alleviation of symptoms. Therefore, when a woman has stopped having hot flashes, for example, the dose is considered to be correct.

Most bHRT practitioners begin treatment with some form of hormone testing, using either saliva, blood or urine to evaluate hormone levels. Although there are many claims about the superiority of one form of testing over another, scientific studies are lacking.

Saliva testing is the least accurate measure of sex hormones. Numerous studies have failed to find a reliable correlation between saliva hormone levels and physiologic (body) hormone levels with the exception of cortisol measurement. (17,44-54)

Blood testing does not reveal the hourly variation and 24-hour cyclical nature of hormone release but it has been better studied. For this reason, blood testing is probably the second-best method of hormone testing.

Twenty-four hour urine testing may be the preferred method of hormone testing. In addition to evaluating hormone output including the 24-hour variation (a “video” instead of a “snapshot,”), urine testing also looks at biochemical intermediates which are independent indicators of hormone levels and hormone metabolism. Some intermediates, such as the 2:16alpha-hydroxyestrone ratio, may be potent predictors of increased risk for hormone-related cancers. (55-56) Fortunately, once known, these risks can be modified.

Dr. Myatt’s Hormone Balance Programs:
Which One is Right for You?

All bHRT programs in both men and women begin with a Brief Telephone Consultation. Together, we determine which program is right for you.

Depending on your age, symptoms, beliefs and what you hope to achieve, we work together to design and implement a complete program to optimize both hormone balance and overall health.

For some men and women, this will include the use of bio-identical hormone replacement therapy, as determined by laboratory testing (24-hour urine). The form may differ depending on which hormones are needed, but usually include both transdermal and oral hormone replacements.

Hormone balance and relief of symptoms can often be achieved without the use of hormone replacement therapy. The decision to use hormones should not be taken lightly and should be made in consultation with a physician who is well-versed in both bHRT and non-hormonal methods of achieving hormone balance.

Which Hormone-Balancing Program is Right for You ?

 The Bronze program is for:

• Peri-menopausal women
• Post-menopausal women
• Men over 35

For women and men desiring better hormone balance  without  the use of
bio-identical hormone replacement.

You will receive a Personalized Health Report and Phone Follow-Up of 60 mins

The Silver program is for:

• Peri-menopausal women
• Post-menopausal women
• Men over 35

For women and men desiring better hormone balance AND bone mineral density protection without using
bio-identical hormone replacement.

You will receive a Personalized Health Report and Phone Follow-Up of 120 mins

The Gold program is for:

• Peri-menopausal women
• Post-menopausal women
• Men over 35

For women and men desiring sex hormone optimization and breast/prostate cancer risk reduction using bHRT.

You will receive a Personalized Health Report and Phone Follow-Up of 360 mins

The Platinum program is for:

• Peri-menopausal women
• Post-menopausal women
• Men over 35

For women and men desiring anti-aging, full-scope endocrine balancing (including sex, thyroid and adrenal hormones) and
breast /prostate cancer risk reduction using bHRT.

You will receive a Personalized Health Report and unlimited Phone Follow-Up

 * saliva hormone testing not available in New York state.

References

1.) Corona G, Rastrelli G, Monami M, Guay A, Buvat J, Sforza A, Forti G, Mannucci E, Maggi M.
Hypogonadism as a risk factor for cardiovascular mortality in men: a meta-analytic study.
Eur J Endocrinol. 2011 Nov;165(5):687-701. Epub 2011 Aug 18.

2.) Corona G, et al “Low testosterone is associated with an increased risk of MACE lethality in subjects with erectile dysfunction” ECE 2010; Poster 149.

3.) Ohlsson C, Barrett-Connor E, Bhasin S, Orwoll E, Labrie F, Karlsson MK, Ljunggren O, Vandenput L, Mellström D, Tivesten A.High Serum Testosterone Is Associated With Reduced Risk of Cardiovascular Events in Elderly Men, J Am Coll Cardiol, 2011; 58:1674-1681

4.) Tivesten A, Mellström D, Jutberger H, Fagerberg B, Lernfelt B, Orwoll E, Karlsson MK, Ljunggren O, Ohlsson C. Low serum testosterone and high serum estradiol associate with lower extremity peripheral arterial disease in elderly men. The MrOS Study in Sweden. J Am Coll Cardiol. 2007 Sep 11;50(11):1070-6. Epub 2007 Aug 24.

5.) Fournier A, Berrino F, Clavel-Chapelon F. Unequal risks for breast cancer associated with different hormone replacement therapies: results from the E3N cohort study. Breast Cancer Res Treat. 2008 Jan;107(1):103-11. Epub 2007 Feb 27.

6.) Fournier A, Berrino F, Riboli E, Avenel V, Clavel-Chapelon F. Breast cancer risk in relation to different types of hormone replacement therapy in the E3N-EPIC cohort. Int J Cancer. 2005 Apr 10;114(3):448-54.

7.) Holtorf K. The bioidentical hormone debate: are bioidentical hormones (estradiol, estriol, and progesterone) safer or more efficacious than commonly used synthetic versions in hormone replacement therapy? Postgrad Med. 2009 Jan;121(1):73-85.

8.) Mahmud K. Natural hormone therapy for menopause. Gynecol Endocrinol. 2010 Feb;26(2):81-5.

9.) Moskowitz D. A comprehensive review of the safety and efficacy of bioidentical hormones for the management of menopause and related health risks. Altern Med Rev. 2006 Sep;11(3):208-23.

10.) Schmidt JW, Wollner D, Curcio J, Riedlinger J, Kim LS. Hormone replacement therapy in menopausal women: Past problems and future possibilities. Gynecol Endocrinol. 2006 Oct;22(10):564-77.

11.) Ichikawa A, Sumino H, Ogawa T, Ichikawa S, Nitta K. Effects of long-term transdermal hormone replacement therapy on the renin-angiotensin- aldosterone system, plasma bradykinin levels and blood pressure in normotensive postmenopausal women. Geriatr Gerontol Int. 2008 Dec;8(4):259-64.

12.) Vilodre LC, Osório Wender MC, Sisson de Castro JA, dos Reis FM, Ruschel S, Magalhães JA,  Spritzer PM. Endometrial response to a cyclic regimen of percutaneous 17beta-estradiol and  low-dose vaginal micronized progesterone in women with mild-to-moderate hypertension.
Gynecol Endocrinol. 2003 Aug;17(4):323-8.

13.) Beral V, Bull D, Reeves G; Million Women Study Collaborators. Endometrial cancer and  hormone-replacement therapy in the Million Women Study. Lancet. 2005 Apr 30-May  6;365(9470):1543-51.

14.) Canonico M, Fournier A, Carcaillon L, et al. Postmenopausal hormone therapy and risk of idiopathic venous thromboembolism: results from the E3N cohort study. Arterioscler Thromb Vasc Biol. 2010;30(2):340-345.

15.) Cirillo DJ, Wallace RB, Rodabough RJ, et al. Effect of estrogen therapy on gallbladder disease. JAMA. 2005;293(3):330-339.

16.)  Eilertsen AL, Høibraaten E, Os I, Andersen TO, Sandvik L, Sandset PM. The effects of oral and transdermal hormone replacement therapy on C-reactive protein levels and other inflammatory markers in women with high risk of thrombosis. Maturitas. 2005;52(2):111-118.

17.)  Files JA, Ko MG, Pruthi S. Bioidentical Hormone Therapy.Mayo Clin Proc. 2011 July; 86(7): 673–680.

18.)  Jacobson BC, Moy B, Colditz GA, Fuchs CS. Postmenopausal hormone use and symptoms of gastroesophageal reflux. Arch Intern Med. 2008;168(16):1798-1804.

19.) Jernström H, Bendahl PO, Lidfeldt J, Nerbrand C, Agardh CD, Samsioe G. A prospective study of different types of hormone replacement therapy use and the risk of subsequent breast cancer: the women’s health in the Lund area (WHILA) study (Sweden). Cancer Causes Control. 2003 Sep;14(7):673-80.

20.)  [No authors listed] Breast cancer and hormone replacement therapy: collaborative reanalysis of data from 51 epidemiological studies of 52,705 women with breast cancer and 108,411 women without breast cancer. Collaborative Group on Hormonal Factors in Breast Cancer. Lancet. 1997 Oct 11;350(9084):1047-59.

21.) de Villiers TJ, Stevenson JC. The WHI: the effect of hormone replacement therapy on fracture prevention. Climacteric. 2012 Jun;15(3):263-6.

22.) Nelson HD, Humphrey LL, Nygren P, Teutsch SM, Allan JD. Postmenopausal hormone replacement therapy: scientific review. JAMA. 2002 Aug 21;288(7):872-81.

23.)  Cramer EH, Jones P, Keenan NL, Thompson BL. Is naturopathy as effective as conventional therapy for treatment of menopausal symptoms? J Altern Complement Med. 2003 Aug;9(4):529-38.

24.)  Ruiz AD, Daniels KR, Barner JC, Carson JJ, Frei CR. Effectiveness of compounded bioidentical hormone replacement therapy: an observational cohort study. BMC Womens Health. 2011 Jun 8;11:27.

25.) Genazzani AR, Pluchino N, Begliuomini S, Stomati M, Bernardi F, Pieri M, Casarosa E, Palumbo M, Genazzani AD, Luisi M. Long-term low-dose oral administration of dehydroepiandrosterone modulates adrenal response to adrenocorticotropic hormone in early and late postmenopausal women. Gynecol Endocrinol. 2006 Nov;22(11):627-35.

26.) Labrie F. DHEA, important source of sex steroids in men and even more in women.
Prog Brain Res. 2010;182:97-148.

27.) Pluchino N, Ninni F, Stomati M, Freschi L, Casarosa E, Valentino V, Luisi S, Genazzani AD, Potì E, Genazzani AR. One-year therapy with 10mg/day DHEA alone or in combination with HRT in postmenopausal women: effects on hormonal milieu. Maturitas. 2008 Apr 20;59(4):293-303. Epub 2008 Apr 3.

28.) Stomati M, Monteleone P, Casarosa E, Quirici B, Puccetti S, Bernardi F, Genazzani AD, Rovati L, Luisi M, Genazzani AR. Six-month oral dehydroepiandrosterone supplementation in early and late postmenopause. Gynecol Endocrinol. 2000 Oct;14(5):342-63.

29.) Aaronson AJ, Morrissey RP, Nguyen CT, Willix R, Schwarz ER. Update on the safety of  testosterone therapy in cardiac disease. Expert Opin Drug Saf. 2011 Sep;10(5):697-704. Epub 2011  Mar 22.

30.) De Maddalena C, Vodo S, Petroni A, Aloisi AM. Impact of testosterone on body fat composition. J Cell Physiol. 2012 Apr 11. doi: 10.1002/jcp.24096. [Epub ahead of print]

31.) Toma M, McAlister FA, Coglianese EE, Vidi V, Vasaiwala S, Bakal JA, Armstrong PW, Ezekowitz  JA. Testosterone supplementation in heart failure: a meta-analysis. Circ Heart Fail. 2012 May

32.) Vermeulen A. Ageing, hormones, body composition, metabolic effects. World J Urol. 2002 May;20(1):23-7.

33.) Vermeulen A, Goemaere S, Kaufman JM. Testosterone, body composition and aging. J Endocrinol Invest. 1999;22(5 Suppl):110-6. 1;5(3):315-21. Epub 2012 Apr 17.

34.)  Shifren JL, Desindes S, McIlwain M, Doros G, Mazer NA. A randomized, open-label, crossover study comparing the effects of oral versus transdermal estrogen therapy on serum androgens, thyroid hormones, and adrenal hormones in naturally menopausal women. Menopause. 2007 Nov-Dec;14(6):985-94.

35.)  L’hermite M, Simoncini T, Fuller S, Genazzani AR. Could transdermal estradiol + progesterone be a safer postmenopausal HRT? A review. Maturitas. 2008 Jul-Aug;60(3-4):185-201. Epub 2008 Sep 5.

36.) Leal M, Díaz J, Serrano E, Abellán J, Carbonell LF. Hormone replacement therapy for oxidative stress in postmenopausal women with hot flushes. Obstet Gynecol. 2000 Jun;95(6 Pt 1):804-9.

37.) Leal Hernández M, Abellán Alemán J, Carbonell Meseguer LF, Díaz Fernández J, García Sánchez FA, Martínez Selva JM. Influence of the presence of hot flashes during menopause on the metabolism of nitric oxide. Effects of hormonal replacement treatment]. Med Clin (Barc). 2000 Jan 22;114(2):41-5.

38.) North American Menopause Society. Treatment of menopause-associated vasomotor symptoms: position statement of The North American Menopause Society. Menopause. 2004 Jan-Feb;11(1):11-33.

39.) McKee J, Warber SL. Integrative therapies for menopause. South Med J. 2005 Mar;98(3):319-26.

40.) Low Dog T. Menopause: a review of botanical dietary supplements. Am J Med. 2005 Dec 19;118 Suppl 12B:98-108.

41.) Kronenberg F, Fugh-Berman A. Complementary and alternative medicine for menopausal symptoms: a review of randomized, controlled trials. Ann Intern Med. 2002 Nov 19;137(10):805-13.

42.) Geller SE, Studee L.Botanical and dietary supplements for menopausal symptoms: what works, what does not. J Womens Health (Larchmt). 2005 Sep;14(7):634-49.

43.) Øverlie I, Moen MH, Holte A, Finset A. Androgens and estrogens in relation to hot flushes during the menopausal transition. Maturitas. 2002 Jan 30;41(1):69-77.

44.) Gröschl M. Current status of salivary hormone analysis. Clin Chem. 2008 Nov;54(11):1759-69. Epub 2008 Aug 29.

45.) Hagen J, Gott N, Miller DR. Reliability of saliva hormone tests. J Am Pharm Assoc . 2003 Nov-Dec;43(6):724-6.

46.) Davison S. Salivary testing opens a Pandora’s box of issues surrounding accurate measurement of testosterone in women. Menopause. 2009;16:630-631.

47.) Flyckt RL, Liu J, Frasure H, Wekselman K, et al. Comparison of salivary versus serum testosterone levels in postmenopausal women receiving transdermal testosterone supplementation versus placebo. Menopause. 2009 Jul-Aug;16(4):680-8.

48.) Granger DA, Shirtcliff EA, Booth A, et al. The “trouble” with salivary testosterone. Psychoneuroendocrinology. 2004 Nov;29(10):1229-40.

49.) Mörelius E, Nelson N, Theodorsson E. Saliva collection using cotton buds with wooden sticks: a note of caution. Scand J Clin Lab Invest. 2006;66(1):15-8.

50.)  6.Lewis JG. Steroid analysis in saliva: an overview. Clin Biochem Rev. 2006 Aug;27(3):139-46.

51.) Stanczyk FZ, Paulson RJ, Roy S. Percutaneous administration of progesterone: blood levels and endometrial protection. Menopause. 2005 Mar;12(2):232-7.

52.) Lewis JG, McGill H, Patton VM, et al. Caution on the use of saliva measurements to monitor absorption of progesterone from transdermal creams in postmenopausal women. Maturitas. 2002 Jan 30;41(1):1-6.

53.) Wren BG, McFarland K, Edwards L, et al. Effect of sequential transdermal progesterone cream on endometrium, bleeding pattern, and plasma progesterone and salivary progesterone levels in postmenopausal women. Climacteric. 2000 Sep;3(3):155-60.

54.) Wood P. Salivary steroid assays – research or routine? . Ann Clin Biochem. 2009 May;46(Pt 3):183-96. Epub 2009 Jan 28.

55.) Kabat GC, Chang CJ, Sparano JA, Sepkovie DW, Hu XP, Khalil A, Rosenblatt R, Bradlow HL.Urinary estrogen metabolites and breast cancer: a case-control study. Cancer Epidemiol Biomarkers Prev. 1997 Jul;6(7):505-9.

56.) Muti P, Bradlow HL, Micheli A, Krogh V, Freudenheim JL, Schünemann HJ, Stanulla M, Yang J, Sepkovic DW, Trevisan M, Berrino F. Estrogen metabolism and risk of breast cancer: a prospective study of the 2:16alpha-hydroxyestrone ratio in premenopausal and postmenopausal women. Epidemiology. 2000 Nov;11(6):635-40.

Dr. Dana Myatt’s Wellness Club

Prescription Fish Oil Now Available!

This just in from the “how dumb does it get?” files…

Enormous amounts of research into the benefits of fish oil have shown that it lowers triglyceride levels, relieves many cases of depression and helps prevent an astonishing number of ailments including osteoporosis, stroke, heart attach, cardiac arrhythmia and some types of cancer. That’s why I’ve been encouraging everyone to add fish oil to their daily health program.

Now, a drug company did another study which showed exactly what we already knew about fish oil—- that it lowers triglyceride levels. They sought and gained FDA approval to offer fish oil as a prescription, at a cost of aprox. 797% more per milligram than Wellness Club brand or other high quality health food store brands. So, instead of a month’s supply at $19.95, you can now enjoy a bottle of 180 caps for $236.89!

As I’ve been warning readers, when the drug companies figure out that a natural substance works, they want a piece of the action. The trouble is, their profit margins will make simple, life-saving natural substances unreachable for most people because of cost.

Meanwhile, There’s even More Reason to Take Fish Oil...

Fish oil could potentially save more lives than cardiac defibrillators, researchers estimate in a new report. In fact, the studies show that the Omega-3 essential fatty acids in fish oil prevent more sudden cardiac deaths due to fibrillation than AED machines. Of course, the makers of these high-tech, high-cost gadgets aren’t going to want you to take fish oil, unless perhaps it’s the $236.89 per bottle prescription brand they can cash in on! What next? Soon we’ll need an Rx. to buy vegetables and fruit at the grocery store because they contain vitamins, minerals and other nutrients!

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More Dangers of Antidepressant Drugs Found

I’ve always been adamant about my treatments for depression, anxiety and other “mood disorders”: go for the fix, not the band aid. No one has ever suffered a case of depression because of a Prozac deficiency!

Now, researchers have found that many antidepressants are even more dangerous than we knew. Paxil, for example, increases violent behavior and suicidal tendencies in users, especially teenagers. EXCUSE ME? Why in the world would we put a child on a dangerous “head med,” one that makes the likelihood of depression-related suicide over twice as high as the un-medicated?

Of course, the FDA is helpful, as always <I say with tongue in cheek>. The have recommended “stronger warning labels” on Paxil. I’m sure most patients especially teens read these labels—Not.

Now here’s a vision – millions of Americans, from children to seniors, all popping what are touted as “happy pills” – at least that is what the Big Pharma Companies and their FDA lapdogs want us to believe. All is not well in this chemical paradise though: Not only do these supposed “happy pills” cause an increased potential for suicide in those taking them (especially in teenagers according to the latest research), they are also linked to violent behavior in what the study calls “hostility events.” What a great idea! Take stressed, depressed, suicidal Americans, driving around in multi-ton Urban Assault vehicles, riding the ragged edge of road rage at the best of times, just waiting to have a “hostility event.” It boggles the mind even more that the FDA has no intention of removing these chemical time-bombs from the marketplace. That would make too much good sense.

Natural Alternatives Treat Depression Without Risks

Paxil, Prozac and other SSRI’s fool the body into temporarily recycling the neurotransmitter serotonin. Of course, not everyone who is depressed has a serotonin deficiency. In fact, epinephrine (adrenaline), noradrenalin, dopamine, acetylcholine are all brain chemicals that can be altered in depression. And even though laboratory tests exist to evaluate neurotransmitters, they are rarely performed by conventional doctors who simply dish out SSRI’s without knowing if this is even going to be a good “band aid.”

The safer and more sensible way to treat depression is to evaluate the neurotransmitters, then use precursors (raw material) nutrients that so the body can naturally make more of its own serotonin, adrenaline, noradrenalin or whatever neurotransmitter is deficient. Instead of simply throwing an SSRI drug at anything that looks like depression, a simple, accurate neuro-transmitter test followed by corrective nutritional therapy is a cure, not a deadly stop-gap.

How many acts of violence will it take before these drugs are removed from the marketplace? Of course, now you can pay 20 times as much for prescription fish oil, which is helpful in many cases of depression, thanks to its approval as a drug. Rest assured that the FDA has Big Pharmacy’s best interests—- not yours— at heart.

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FDA Defends Deadly Vioxx, More Proof of Their Allegiance

Vioxx has been found in several major studies to be the most dangerous COX-2 inhibitor drug, increasing the risk of irregular heart rhythms AND kidney disease according to Researchers at The Department of Epidemiology and Nutrition at Harvard School of Public Health. A second study at the University of Newcastle in Australia looked at 500,000 healthy people who used Vioxx and found that as drug dosage increased, so did the rate of heart attacks.

Eric Ding, who co-authored the Harvard study, felt strongly that “The risks of these drugs should have been made known to the public much earlier.”

Dr. David J. Graham, associate director for science in the FDA’s Office of Drug Safety, blew the whistle on both Vioxx maker Merck and the FDA itself, stating “It is clear that Vioxx increases the risk of heart attack, and that increase in risk begins with the first tablet a patient takes.”

In spite of the known dangers and mounting evidence against Vioxx, the FDA offered a “spin control” press release stating that “the FDA does not believe the available data rise to the level required to support an official FDA regulatory decision regarding comparative safety and efficacy of the available COX2-selective and non-selective NSAIDs.”

Don’t you sleep better knowing that the FDA is “protecting” us from affordable, safe, proven remedies like fish oil while ensuring that dangerous drugs such as Paxil and Vioxx remain on the market? I know I do.

In Health,
Dr. Myatt

Fiber:

Twenty-Five Surprising Benefits of  a Dietary “Non-Nutrient”

It’s not a “sexy supplement” or a “new breakthrough.” In fact, it’s not even officially classified as a nutrient. But Americans get only 10% of the amount we consumed 100 years ago, and our health may be seriously suffering as a result.

What is this important “non nutrient” that we’re missing? Dietary fiber.

“Fiber” refers to a number of indigestible carbohydrates found in the outer layers of plants. Humans lack enzymes to break down most types of fiber, so they pass through the digestive system relatively unchanged and do not provide nutrients or significant calories.

In spite of this indigestibility, fiber has a surprising number of health benefits. In fact, consuming adequate daily fiber may be one of the most important health measures anyone can take.

Twenty-Five Health Benefits of Fiber — Who Knew?

There are numerous “sub-classes” of fiber, but the two main types are I.) soluble and II.) insoluble fiber. Both types are beneficial to health and both typically occur together in nature. They each offer independent health benefits. Here are twenty-five known health benefits that fiber provides.

Bowel Benefits:

  1. Relieves constipation. Insoluble fiber absorbs large amounts of water in the colon. This makes stools softer and easier to pass. Most people who increase fiber intake will notice improved bowel function in 31-39 hours.(1-4)
  2. Relieves diarrhea. It may seem paradoxical that a substance which helps constipation also helps diarrhea, but that’s just what fiber does. Insoluble fiber binds watery stool in the colon, helping turn “watery” into “formed.” Fiber is known to offer significant improvement to those with diarrhea.(5,6)
  3. Helps prevent hemorrhoids. Constipation is a leading cause of hemorrhoids. Because fiber-rich stools are easier to pass, less straining is necessary. Diets high in fiber have been shown to prevent and relieve hemorrhoids.(7)
  4. Reduces risk of diverticular disease. In cultures that consume high-fiber diets, diverticular disease is relatively unknown. That’s because high fiber intake “exercises” the colon, prevents excess bowel gas and absorbs toxins, all of which lead to the “bowel herniation” disease known as diverticulitis. Increased fiber intake is currently recommended in Western medicine as primary prevention for the disease.(8,9,10)
  5. Helps Irritable bowel syndrome (IBS). IBS is characterized by constipation, diarrhea, or alternating constipation/diarrhea. Regardless of type, increased fiber intake has been shown to improve IBS symptoms.(3,11-14)
  6. Improves bowel flora. “Flora” refers to the “good bugs” (healthy bacteria) that colonize the large intestine (colon). Antibiotics, drugs, food allergies, high sugar diets and junk food alter this “bowel garden” in favor of the “bad bugs.” Certain types of fiber are rich in substances the “feed” bowel flora and help keep the balance of good bacteria in the colon at a normal level.(4,15)
  7. Helps prevent colon cancer. Although research has been controversial, observational studies in the 1970s showed that African natives consuming high-fiber diets had a much lower incidence of colorectal carcinoma.(16) Since the “risk” of increased fiber consumption is so small, the “US Pharmacist,” states…

“…with no clearly negative data about fiber, it makes sense to increase fiber intake just in case the positive studies did reveal an actual link. The patient will also experience the ancillary benefits of fiber consumption, such as reduction in cholesterol (with psyllium), prevention of constipation, and reducing risk of hemorrhoids.”

  1. Appendicitis: studies show a correlation between the development of appendicitis and low fiber intake. A diet high in fiber may help prevent appendicitis.(59)

Whew… that’s just the bowel benefits!
Fiber also helps prevent heart disease in multiple ways.

  1. Lowers Total cholesterol. According to the FDA, soluble fiber meets the standard for reduction of risk from coronary heart disease.(15,16) Psyllium husk is also able to reduce the risk of coronary heart disease as it contains a soluble fiber similar to beta-glucan.(17-26)
  2. Lowers triglycerides. Higher dietary fiber is associated with lower triglyceride levels.(24-26)
  3. Raises HDL. Fiber may even raise HDL — the “good cholesterol” — levels.(27)
  4. Lowers LDL Cholesterol. In addition to total cholesterol, increased fiber lowers LDL — the “bad cholesterol” — levels.(28-29)
  5. Aids Weight loss. Fiber helps prevent weight gain and assists weight loss several ways. The “bulking action” of fiber leads to an earlier feeling of satiety, meaning that one feels satisfied with less high-calorie food when the meal contains a lot of fiber.(30,31) Fiber helps bind and absorb dietary fat, making it less available for assimilation. This means that some fat may be “lost” through the digestive tract when the meal is high in insoluble fiber.(32)
  6. Lowers Overall risk of Coronary Artery Disease. Perhaps because of a combination of the above-listed lipid-normalizing factors, some studies have shown an overall protective effect of higher fiber intake against coronary heart disease.(33)

Fiber also benefits blood sugar levels and diabetes…

  1. Helps Type I Diabetes. Eaten with meals, high-fiber supplements like guar gum reduced the rise in blood sugar following meals in people with type 1 diabetes.(34-35) In one trial, a low-glycemic-index diet containing 50 grams of daily fiber improved blood sugar control and helped prevent hypoglycemic episodes in people with type 1 diabetes taking two or more insulin injections per day.(36)
  2. Improves Type II Diabetes. High-fiber diets have been shown to work better in controlling diabetes than the American Diabetic Association (ADA)-recommended diet, and may control blood sugar levels as well as oral diabetic drugs.One study compared participants eating the the ADA diet (supplying 24 grams of daily fiber) or a high-fiber diet (containing 50 grams daily fiber) for six weeks. Those eating the high-fiber diet for six weeks had an average 10% lower glucose level than people eating the ADA diet. Insulin levels were 12% lower in the high-fiber group compared to those in the ADA diet group. The high fiber group also had decreased  glycosylated hemoglobin levels, a measure of long-term blood glucose regulation.(37)

    High-fiber supplements such as psyllium(38),  guar gum(39) and pectin(40) have shown improved glucose tolerance.(20, 26)

More systemic benefits of fiber:

  1. Gallstone prevention. Rapid digestion of carbohydrates leads to fast release of glucose (sugar) into the bloodstream. In response, the body releases large amounts of insulin. High insulin levels contribute to gallstone formation. Because dietary fiber slows the release of carbohydrates (and corresponding insulin), fiber helps prevent gallstone formation.(41-43)
  2. Kidney stone prevention. Low intakes of dietary fiber have been found to correlate with increased kidney stone formation, and higher intakes of fiber appear to be protective against stone formation.(44-46)
  3. Varicose veins. “Straining at stool” caused by fiber-deficiency constipation, has been found in some studies to cause varicose veins.(47) Populations with lower fiber intakes have higher rates of varicosities.(48)

Fiber may even be important in prevention of certain types of cancer…

  1. Colon Cancer Prevention. Diets higher in fiber have been shown in some studies to reduce the risk of colon cancer.(49-51)
  2. Breast cancer prevention. Higher fiber diets are associated with lower breast cancer risk.(51,52) Some studies have shown up to a 50% decreased risk with higher fiber intakes.(53) After diagnosis, a high fiber diet may decrease the risk of  breast cancer reoccurrence.(54)
  3. Pancreatic cancer prevention. High fiber diets are associated with lower risk of pancreatic cancer.(55)
  4. Endometrial cancer prevention. Higher fiber has been shown in some studies to protect against endometrial cancer.(56)
  5. Prostate cancer prevention. Diets higher in fiber may be associated with lower risk of prostate cancer.(51,57) After diagnosis, a high fiber diet may decrease the risk of  prostate cancer reoccurrence.(54)
  6. Cancer prevention in general. Some studies have found that high fiber diets help prevent cancer in general, regardless of type.(58)

Recommendations vs. Reality

The average daily American fiber intake is estimated at 14 to 15 g, significantly less than the American Dietetic Association recommendation of 20 to 35 g for adults, 25 g daily for girls ages 9 through 18 years and 31 to 38 g for boys ages 9 through 18.(60-61) The American Heart Association recommends 25 to 30 g daily.(62)

Based on dietary intakes of long-lived populations (who typically consume 40-60 grams or more of fiber per day), many holistic physicians recommend aiming for a minimum of 30 grams of daily fiber.

In my clinical experience, I find that most people over-estimate their fiber intake because they are unaware of the fiber content of many of the foods they eat. See how your food choices stack up here: Rate Your Plate – It’s fun, educational and surprising!

Since fiber has proven itself to be such an important “non nutrient” for good health, increased dietary consumption and/or supplementation can be considered a wise choice for optimal health and disease prevention.

EZ-FiberStill The Best-Tasting, Most Complete Fiber Available

Dr. Myatt’s Maxi Fiber was called EZ Fiber – NOW CALLED Fiber Complex

Great News! Maxi Fiber, one of Dr. Myatt’s most popular products, has been licensed to a major supplement manufacturer. This means that Dr. Myatt no longer sells Maxi Fiber in the small containers, but now offers the same great product (exactly the same!) in a larger container for your convenience. The old Maxi Fiber provided 30 servings per container and the new product Fiber Complex ™ comes in a 60 serving container.

Click Here To Order Fiber Complex

References

  1. Constipation. Am Fam Physician . 2005;71:539-540.
  2. Mauk KL. Preventing constipation in older adults. Nursing. 2005;35:22-23.
  3. Slavin JL, Greenberg NA. Partially hydrolyzed guar gum: clinical nutrition uses.Nutrition. 2003 Jun;19(6):549-52.
  4. Takahashi H, Wako N, Okubo T, Ishihara N, Yamanaka J, Yamamoto T.Influence of partially hydrolyzed guar gum on constipation in women. J Nutr Sci Vitaminol (Tokyo). 1994 Jun;40(3):251-9.
  5. Nakamura S, Hongo R, Moji K, Oku T. Suppressive effect of partially hydrolyzed guar gum on transitory diarrhea induced by ingestion of maltitol and lactitol in healthy humans.Eur J Clin Nutr. 2007 Sep;61(9):1086-93. Epub 2007 Jan 24.
  6. Homann HH, Kemen M, Fuessenich C, Senkal M, Zumtobel V. Reduction in diarrhea incidence by soluble fiber in patients receiving total or supplemental enteral nutrition. JPEN J Parenter Enteral Nutr. 1994 Nov-Dec;18(6):486-90.
  7. Alonso-Coello P, Mills E, Heels-Ansdell D, López-Yarto M, Zhou Q, Johanson JF, Guyatt G. Fiber for the treatment of hemorrhoids complications: a systematic review and meta-analysis. Am J Gastroenterol. 2006 Jan;101(1):181-8.
  8. Korzenik JR. Case closed? Diverticulitis: epidemiology and fiber. J Clin Gastroenterol. 2006 Aug;40(7 Suppl 3):S112-6.
  9. Frieri G, Pimpo MT, Scarpignato C. Management of colonic diverticular disease. Digestion. 2006;73 Suppl 1:58-66. Epub 2006 Feb 8.
  10. Salzman H, Lillie D. Diverticular disease: diagnosis and treatment. Am Fam Physician. 2005 Oct 1;72(7):1229-34
  11. Fielding JF, Melvin K. Dietary fibre and the irritable bowel syndrome. J Hum Nutr. 1979 Aug;33(4):243-7.
  12. Parisi GC, Zilli M, Miani MP, Carrara M, Bottona E, Verdianelli G, Battaglia G, Desideri S, Faedo A, Marzolino C, Tonon A, Ermani M, Leandro G. High-fiber diet supplementation in patients with irritable bowel syndrome (IBS): a multicenter, randomized, open trial comparison between wheat bran diet and partially hydrolyzed guar gum (PHGG). Dig Dis Sci. 2002 Aug;47(8):1697-704.
  13. Parisi G, Bottona E, Carrara M, Cardin F, Faedo A, Goldin D, Marino M, Pantalena M, Tafner G, Verdianelli G, Zilli M, Leandro G. Treatment effects of partially hydrolyzed guar gum on symptoms and quality of life of patients with irritable bowel syndrome. A multicenter randomized open trial. Dig Dis Sci. 2005 Jun;50(6):1107-12.
  14. Giannini EG, Mansi C, Dulbecco P, Savarino V. Role of partially hydrolyzed guar gum in the treatment of irritable bowel syndrome. Nutrition. 2006 Mar;22(3):334-42. Epub 2006 Jan 18.
  15. Giannini EG, Mansi C, Dulbecco P, Savarino V. Role of partially hydrolyzed guar gum in the treatment of irritable bowel syndrome. Nutrition. 2006 Mar;22(3):334-42. Epub 2006 Jan 18.
  16. Franco A, Sikalidis AK, Solis Herruzo JA. Colorectal cancer: Influence of diet and lifestyle factors. Rev Esp Enferm Dig. 2005;97:432-448.
  17. Chandalia M, Garg A, Lutjohann D, et al. Beneficial effects of high dietary fiber intake in patients with type 2 diabetes mellitus. New Engl J Med 2000;342:1392–8.
  18. Rodríguez-Morán M, Guerrero-Romero F, Lazcano-Burciaga G. Lipid- and glucose-lowering efficacy of plantago psyllium in type II diabetes. Diabetes Its Complications 1998;12:273–8.
  19. Landin K, Holm G, Tengborn L, Smith U. Guar gum improves insulin sensitivity, blood lipids, blood pressure, and fibrinolysis in healthy men. Am J Clin Nutr 1992;56:1061–5.
  20. Stasse-Wolthuis M, Hautvast JG, Hermus RJ, Katan MB, Bausch JE, Rietberg-Brussaard JH, Velema JP, Zondervan JH, Eastwood MA, Brydon WG. The effect of a natural high-fiber diet on serum lipids, fecal lipids, and colonic function. Am J Clin Nutr. 1979 Sep;32(9):1881-8.
  21. Jenkins DJ, Wolever TM, Rao AV, Hegele RA, Mitchell SJ, Ransom TP, Boctor DL, Spadafora PJ, Jenkins AL, Mehling C, et al. Effect on blood lipids of very high intakes of fiber in diets low in saturated fat and cholesterol. N Engl J Med. 1993 Jul 1;329(1):21-6.
  22. Jenkins DJ, Kendall CW, Popovich DG, Vidgen E, Mehling CC, Vuksan V, Ransom TP, Rao AV, Rosenberg-Zand R, Tariq N, Corey P, Jones PJ, Raeini M, Story JA, Furumoto EJ, Illingworth DR, Pappu AS, Connelly PW. Effect of a very-high-fiber vegetable, fruit, and nut diet on serum lipids and colonic function. Metabolism. 2001 Apr;50(4):494-503.
  23. Minekus M, Jelier M, Xiao JZ, Kondo S, Iwatsuki K, Kokubo S, Bos M, Dunnewind B, Havenaar R. Effect of partially hydrolyzed guar gum (PHGG) on the bioaccessibility of fat and cholesterol. Biosci Biotechnol Biochem. 2005 May;69(5):932-8.
  24. Kondo S, Xiao JZ, Takahashi N, Miyaji K, Iwatsuki K, Kokubo S. Suppressive effects of dietary fiber in yogurt on the postprandial serum lipid levels in healthy adult male volunteers. Biosci Biotechnol Biochem. 2004 May;68(5):1135-8.
  25. Bhargava A. Fiber intakes and anthropometric measures are predictors of circulating hormone, triglyceride, and cholesterol concentrations in the women’s health trial. J Nutr. 2006 Aug;136(8):2249-54.
  26. Higgins JA. Resistant starch: metabolic effects and potential health benefits. J AOAC Int. 2004 May-Jun;87(3):761-8.
  27. Solà R, Godàs G, Ribalta J, Vallvé JC, Girona J, Anguera A, Ostos M, Recalde D, Salazar J, Caslake M, Martín-Luján F, Salas-Salvadó J, Masana L. Effects of soluble fiber (Plantago ovata husk) on plasma lipids, lipoproteins, and apolipoproteins in men with ischemic heart disease. Am J Clin Nutr. 2007 Apr;85(4):1157-63
  28. Aller R, de Luis DA, Izaola O, La Calle F, del Olmo L, Fernandez L, Arranz T, Hernandez JM. Effect of soluble fiber intake in lipid and glucose levels in healthy subjects: a randomized clinical trial. Diabetes Res Clin Pract. 2004 Jul;65(1):7-11
  29. Wood RJ, Fernandez ML, Sharman MJ, Silvestre R, Greene CM, Zern TL, Shrestha S, Judelson DA, Gomez AL, Kraemer WJ, Volek JS. Effects of a carbohydrate-restricted diet with and without supplemental soluble fiber on plasma low-density lipoprotein cholesterol and other clinical markers of cardiovascular risk. Metabolism. 2007 Jan;56(1):58-67.
  30. Higgins JA. Resistant starch: metabolic effects and potential health benefits. J AOAC Int. 2004 May-Jun;87(3):761-8.
  31. Cani PD, Joly E, Horsmans Y, Delzenne NM. Oligofructose promotes satiety in healthy human: a pilot study. Eur J Clin Nutr. 2006 May;60(5):567-72.
  32. van Bennekum AM, Nguyen DV, Schulthess G, Hauser H, Phillips MC. Mechanisms of cholesterol-lowering effects of dietary insoluble fibres: relationships with intestinal and hepatic cholesterol parameters. Br J Nutr. 2005 Sep;94(3):331-7.
  33. Jensen MK, Koh-Banerjee P, Hu FB, Franz M, Sampson L, Grønbaek M, Rimm EB. Intakes of whole grains, bran, and germ and the risk of coronary heart disease in men. Am J Clin Nutr. 2004 Dec;80(6):1492-9.
  34. U.S. Department of Agriculture, U.S. Department of Health and Human Services: Dietary Guidelines for Americans, 2005. Home and Garden Bulletin No. 232, 2005. Available from URL: www.health.gov/dietaryguidelines/dga2005/document.
  35. Ebeling P, Yki-Jarvinen H, Aro A, et al. Glucose and lipid metabolism and insulin sensitivity in type 1 diabetes: the effect of guar gum. Am J Clin Nutr 1988;48:98–103.
  36. Giacco R, Parillo M, Rivellese AA, et al. Long-term dietary treatment with increased amounts of fiber-rich low-glycemic index natural foods improves blood glucose control and reduces the number of hypoglycemic events in type 1 diabetic patients. Diabetes Care 2000;23:1461–6.
  37. Fed Reg. 1997;62(99):28234-28245.
  38. Fed Reg. 1998;63(32):8103-8121
  39. Moreyra AE, Wilson AC, Koraym A. Effect of combining psyllium fiber with simvastatin in lowering cholesterol. Arch Intern Med. 2005;165:1161-1166.
  40. Schwartz SE, Levine RA, Weinstock RS, et al. Sustained pectin ingestion: effect on gastric emptying and glucose tolerance in non-insulin-dependent diabetic patients. Am J Clin Nutr 1988;48:1413–7.
  41. Mendez-Sanchez N, Zamora-Valdes D, Chavez-Tapia NC, Uribe M.  Role of diet in cholesterol gallstone formation.Clin Chim Acta. 2007 Feb;376(1-2):1-8. Epub 2006 Sep 15.
  42. Cuevas A, Miquel JF, Reyes MS, Zanlungo S, Nervi F. Diet as a risk factor for cholesterol gallstone disease. J Am Coll Nutr. 2004 Jun;23(3):187-96.
  43. Schwesinger WH, Kurtin WE, Page CP, Stewart RM, Johnson R.. Soluble dietary fiber protects against cholesterol gallstone formation. Am J Surg. 1999 Apr;177(4):307-10.
  44. Griffith HM, O’Shea B, Kevany JP, McCormick JS. A control study of dietary factors in renal stone formation. Br J Urol. 1981 Oct;53(5):416-20.
  45. Jaeger P. Prevention of recurrent calcium stones: diet versus drugs. Miner Electrolyte Metab. 1994;20(6):410-3
  46. Ebisuno S, Morimoto S, Yoshida T, et al. Rice-bran treatment for calcium stone formers with idiopathic hypercalciuria. Br J Urol 1986;58:592–5.
  47. Burkitt DP. Varicose veins: facts and fantasy. Arch Surg. 1976 Dec;111(12):1327-32.
  48. Richardson JB, Dixon M. Varicose veins in tropical Africa.Lancet. 1977 Apr 9;1(8015):791-2.
  49. Jenkins DJ, Kendall CW, Popovich DG, Vidgen E, Mehling CC, Vuksan V, Ransom TP, Rao AV, Rosenberg-Zand R, Tariq N, Corey P, Jones PJ, Raeini M, Story JA, Furumoto EJ, Illingworth DR, Pappu AS, Connelly PW. Effect of a very-high-fiber vegetable, fruit, and nut diet on serum lipids and colonic function. Metabolism. 2001 Apr;50(4):494-503.
  50. Le Marchand L, Hankin JH, Wilkens LR, Kolonel LN, Englyst HN, Lyu LC. Dietary fiber and colorectal cancer risk. Epidemiology. 1997 Nov;8(6):658-65.
  51. Divisi D, Di Tommaso S, Salvemini S, Garramone M, Crisci R. Diet and cancer. Acta Biomed. 2006 Aug;77(2):118-23.
  52. Saarinen NM, Wärri A, Airio M, Smeds A, Mäkelä S. Role of dietary lignans in the reduction of breast cancer risk. Mol Nutr Food Res. 2007 Jul;51(7):857-66.
  53. Suzuki R, Rylander-Rudqvist T, Ye W, Saji S, Adlercreutz H, Wolk A. Dietary fiber intake and risk of postmenopausal breast cancer defined by estrogen and progesterone receptor status-A prospective cohort study among Swedish women. Int J Cancer. 2007 Aug 31; [Epub ahead of print].
  54. Ferdowsian HR, Barnard ND. The role of diet in breast and prostate cancer survival. Ethn Dis. 2007 Spring;17(2 Suppl 2):S2-18-22.
  55. Chan JM, Wang F, Holly EA. Whole grains and risk of pancreatic cancer in a large population-based case-control study in the San Francisco Bay Area, California. Am J Epidemiol. 2007 Nov 15;166(10):1174-85. Epub 2007 Sep 18.
  56. Goodman MT, Wilkens LR, Hankin JH, Lyu LC, Wu AH, Kolonel LN. Association of soy and fiber consumption with the risk of endometrial cancer. Am J Epidemiol. 1997 Aug 15;146(4):294-306.
  57. Kolonel LN, Hankin JH, Whittemore AS, Wu AH, Gallagher RP, Wilkens LR, John EM, Howe GR, Dreon DM, West DW, Paffenbarger RS Jr. Vegetables, fruits, legumes and prostate cancer: a multiethnic case-control study. Cancer Epidemiol Biomarkers Prev. 2000 Aug;9(8):795-804.
  58. Donaldson MS. Nutrition and cancer: a review of the evidence for an anti-cancer diet. Nutr J. 2004 Oct 20;3:19.
  59. Adamidis D, Roma-Giannikou E, Karamolegou K, Tselalidou E, Constantopoulos A. Fiber intake and childhood appendicitis. Int J Food Sci Nutr. 2000 May;51(3):153-7.
  60. Eat fiber for health. American Dietetic Association. Available at: www.webdietitians.org/Public/index_20411.cfm. Accessed April 11, 2006.
  61. elp your children meet their fiber needs. Available at: www.eatright.org/cps/rde/xchg/ada/hs.xsl/home_4309_ENU_HTML.htm. Accessed April 11, 2006.
  62. Fiber. American Heart Association. Available at: www.americanheart.org/presenter.jhtml?identifier=4574. Accessed April 11, 2006.

Lutein Plus 20 mg 30 capsules

Nature’s Secret for Healthy Eyes

Lutein (pronounced loo’teen) is in the carotenoid family, as is the better-known beta carotene. Carotenoids are the natural colorant or pigments found in dark green leafy vegetables such as spinach and in egg yolks.

Lutein levels correlate with healthy eyes, apparently reducing the risk of macular degeneration. A correlation is also seen with higher lutein levels and healthy skin.

Lutein when taken as a supplement or eaten in foods is naturally deposited as a protective layer in the macula, the small spot in the back of the eye that is responsible for central vision.

This layer, known as macular pigment, works like sunglasses inside your eyes protecting them from damaging light – especially blue light. This is similar to the way orange colored lenses in “glare-reducing” or “contrast-enhancing” driving glasses work.

Healthy macular pigment can improve your ability to react to bright flashes of light (like from those obnoxious blue headlights at night) or see objects against a similar background – critical to driving at night or enjoying outdoor sports.

To keep eyes healthy and protect them as they age, research indicates that people need at least 10 mg. of lutein everyday through dietary sources and supplemental lutein.

The New AREDS2 Results and Recommendations:

The National Eye Institute has provided new recommendation for AREDS2 formulations based on it’s landmark AREDS2 study. NEI’s recommendation adds 10 mg. lutein and 2 mg. zeaxanthin and eliminates beta carotene in the original AREDS supplement.

Results from AREDS2 report a 18% reduction in progression to advanced AMD in subjects who received 10 mg. Lutein and 2 mg. Zeaxanthin, in addition to an AREDS supplement without beta carotene when compared to the original AREDS supplement with beta carotene.

The reduction in progression to advanced AMD is even greater (26%) in those people who have the lowest intake of lutein and zeaxanthin in their diet. In the US, the dietary intake of lutein and zeaxanthin is usually less than 1 mg. per day for most people – well below the 10 mg. lutein and 2 mg. zeaxanthin that the study has proven to be effective.

Antioxidant Properties

Lutein is an antioxidant that appears to quench or reduce harmful free radicals in various parts of the body. Free radicals can play a role in a variety of chronic diseases, including cataracts and macular degeneration.

Lutein and Glare Disability

Glare Disability is common in older adults and can be worsened by conditions such as cataracts. It encompases a variety of complaints, from decreased visual acuity or quality (chromatic contrast) in “glare” light conditions to decreased ability to recover from exposure to flashes of bright light (photostress recovery).

A study published in 2014 states:

“CONCLUSIONS: Daily supplementation with L+Z [Lutein plus Zeaxanthin] resulted in significant increase in serum levels and MPOD [macular pigment optical density] and improvements in chromatic contrast and recovery from photostress. These results are consistent with past studies showing that increasing MPOD leads to improved visual performance. “

Lutein filters the high-energy, blue wavelengths of light from the visible-light spectrum. Blue light, in both indoor lighting and sunlight, is believed to induce oxidative stress and possible free-radical damage in human organs exposed to light, such as the eyes and skin. Blue light is not the same as the commonly known ultraviolet A and ultraviolet B wavelengths of the invisible spectrum.

Most Americans get insufficient lutein in their diets. Research suggests that 6 to 20 mg. of lutein per day are needed to realize its health benefits.

Common food sources of Lutein and Zeaxanthin include:
Product- Lutein/zeaxanthin / micrograms per hundred grams
kale – (raw)39,550 (cooked)18,246
turnip greens – (raw)12,825
spinach – (raw)12,198 (cooked)11,308
swiss chard (raw or cooked)11,000
turnip greens (cooked)8440
collard greens (cooked)7694
watercress (raw)5767
garden peas (raw)2593
romaine lettuce2312
zucchini2125
brussels sprouts1590
pistachio nuts1205
broccoli1121
carrot (cooked)687
Maize/corn642
egg (hard boiled)353
avocado (raw)271
carrot (raw)256
kiwifruit122

Remember, 100 grams is 0.22 lb. – almost a quarter of a pound. 1 microgram (mcg) is .001 mg. or 1/100th of a milligram. So, if you were to eat a quarter pound of raw kale you would get around 39.5 milligrams (mg.) of Lutein/Zeaxanthin. I recently brought home a bunch of kale from the grocery store, and it weighed just under a half pound, stems and all.

Lutein Plus+ contains maximum amounts of Lutein, along with Zeaxanthin, another powerful carotenoid antioxidant that has been shown to be highly beneficial and protective to the eyes. Further increasing the antioxidant properties are Bilberry and Vitamin E.

Each (one) capsule contains:
Lutein 20 mg. (from Marigold [Calendula officinalis] flowers)
Zeaxanthin 880 mcg (from Marigold [Calendula officinalis] flowers)
Bilberry fruit powder (Vaccinium mytrillus) 25 mg.
Vitamin E 1 IU (as natural mixed tocopherols)

References and further reading:

AREDS2 study: http://www.areds2.org/

Associations between age-related nuclear cataract and lutein and zeaxanthin in the diet and serum in the Carotenoids in the Age-Related Eye Disease Study, an Ancillary Study of the Women’s Health Initiative. http://www.ncbi.nlm.nih.gov/pubmed/18332316

Studies of the effects of dietary supplementation, primarily with preparations including lutein and zeaxanthin, have demonstrated improvements in contrast sensitivity and visual performance under glare conditions… http://www.ncbi.nlm.nih.gov/pubmed/20590393

Relation among serum and tissue concentrations of lutein and zeaxanthin and macular pigment density http://ajcn.nutrition.org/content/71/6/1555.full

Hammond BR et.al. A double-blind, placebo-controlled study on the effects of lutein and zeaxanthin on photostress recovery, glare disability, and chromatic contrast. Invest Ophthalmol Vis Sci. 2014 Dec 2;55(12):8583-9. doi: 10.1167/iovs.14-15573. http://www.ncbi.nlm.nih.gov/pubmed/25468896

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Sugar More Addictive Than Cocaine According To New Research!

08/23/07

This Week In HealthBeat News:

  • Yet More Good Reasons To Stop The Pop Habit – Metabolic Syndrome And Addiction
  • This week’s FDA “Warnings”…
  • The FDA Is “At It Again”… Keeping Us Safe From Mother Nature
  • We Get Letters I –  Comments and Questions…
  • We Get Letters II – Readers Ask Medical Questions…
  • Laughter is Good Medicine: Kids Say The Darndest Things – Part 2

Yet More Good Reasons To Stop The Pop Habit

Dr. Myatt has written and warned and ranted about the dangers of Soda Pop consumption over and over and over – most recently in our HealthBeat article Poisonous Pop . Well, the bad news about pop just keeps rolling in… this article from one of the many medical journals that we read each day for you:


A study suggests that middle-aged adults who drink more than 1 soft drink (diet or regular) daily have a higher risk of developing adverse metabolic traits as well as the metabolic syndrome.
Medscape Medical News 2007

For those who are a little hazy about what is “metabolic syndrome”, the article defines it thusly:

Metabolic syndrome was defined as the presence of three or more of following risk factors: excess waist circumference, high blood pressure, elevated triglycerides, low high-density lipoprotein (HDL)-cholesterol levels, and high fasting glucose levels. [high fasting glucose levels = diabetes]

So, the long and short of this is that Pop drinkers are far more likely to develop “Metabolic Syndrome” and diabetes and cardiovascular disease. Cool, huh? And we let our kids drink this stuff ???

But Wait! There’s More!

This just in from a research paper out of France:

Intense Sweetness Surpasses Cocaine Reward

Yup, you read correctly – according to this study sugar is more addicting than cocaine!

Here is the conclusion of the research (edited slightly for brevity):

Our findings clearly demonstrate that intense sweetness can surpass cocaine reward, … We speculate that the addictive potential of intense sweetness results from an inborn hypersensitivity to sweet tastants. In … humans, sweet receptors evolved in ancestral environments poor in sugars and are thus not adapted to high concentrations of sweet tastants. The supranormal stimulation of these receptors by sugar-rich diets, such as those now widely available in modern societies, would generate a supranormal reward signal in the brain, with the potential to override self-control mechanisms and thus to lead to addiction.

Here’s the short-course, plain English translation: Because our distant (and not-so-distant) ancestors developed without mounds of sugar available to them we don’t handle sugars well, and sugars turn out to be actually more addictive (in the truest sense of addiction) than cocaine. Further, it is not the sugar, but the intense sweetness that is the addictive thing – the researchers used saccharine as a sweetener as well as sucrose (sugar) and the results were the same. Sweet beat out cocaine for the lab rats in the study.

Yikes! It boggles the mind, doesn’t it!

Read the research paper in it’s entirety here: http://www.plosone.org/article/fetchArticle.action?articleURI=info%3Adoi%2F10.1371%2Fjournal.pone.0000698

Still gonna go out for that six-pack of soda-pop or that mega-slurpee at the convenience store? Why not try some alternatives? Plain ol’ water has been a perennial favorite since the days of Alley Oop the caveman – I’ve heard it called “Adam’s Ale”… but if water just doesn’t cut it for you, how about iced green tea with a little lemon, or if you really need an energy drink, try some Greens First Berry  – 10 Servings of Fruits & Vegetables in One Delicious Drink, with minimal sugar.

This week’s FDA “Warnings”…

Certain Diabetes Drugs to Carry Strengthened Warnings
Manufacturers of certain drugs to treat type 2 diabetes have agreed to add a stronger warning on the risk of heart failure. The information will be included in the form of a “boxed” warning, FDA’s strongest type of warning.
FDA

So… take Big Pharma’s drugs and risk heart failure, or read up on some natural strategies for dealing with Diabetes without drugs and risk improving your health… Tough call, right? Check out our webpage Diabetes – get hip, get healthy, and do it without heart-destroying drugs!

Updated Prescribing Information Approved for Coumadin
FDA has approved updated labeling for the blood-thinning drug Coumadin to explain that genetic makeup may influence how a patient responds to the drug. Manufacturers of warfarin, the generic version of Coumadin, also plan to add similar labeling information.
FDA News

It should come as no surprise that there are some wonderfully effective ways of maintaining healthy blood “viscosity” and normal clotting factors that don’t involve swallowing “rat poison’… you can find plenty of free information with strategies for staying healthy without rat poison – check out our pages on Thrombophlebitis and Heart Health and kick the Warfarin habit before it kicks you!

The FDA Is “At It Again”… Keeping Us Safe From Mother Nature

A recent notice from the FDA warns consumers to not use several red yeast rice products that have been discovered to contain a molecule described as Lovastatin – the molecule synthesized by the Big Drug Companies and marketed to us under a variety of brand names such as Mevacor®, Advicor®, Altocor®,
Altoprev®, and Statosan® (Atos Pharma).

Here is their warning and link for your amusement:

FDA is warning consumers not to buy or eat three red yeast rice products promoted and sold online as dietary supplements for treating high cholesterol. FDA analysis showed the products contained an ingredient found in the prescription cholesterol drug Mevacor. FDA News

In part, their warning states:

This risk is even more serious because consumers may not know the side effects associated with lovastatin and the fact that it can adversely interact with other medications,” said Steven Galson, M.D., M.P.H., director of FDA’s Center for Drug Evaluation and Research.

Oooh! Spooky frightening words! No mention of course that the FDA approved drug, which is the same stuff that is in the supplements the FDA would ban, might be just as dangerous (or not)…

The FDA goes on to explain:

These red yeast rice products are a threat to health because the possibility exists that lovastatin can cause severe muscle problems leading to kidney impairment. This risk is greater in patients who take higher doses of lovastatin or who take lovastatin and other medicines that increase the risk of muscle adverse reactions. These medicines include the antidepressant nefazodone, certain antibiotics, drugs used to treat fungal infections and HIV infections, and other cholesterol-lowering medications.

Uh, Guys…? You forgot grapefruit juice – grapefruit juice (and grapefruit) inhibits the metabolism of statins which can increase the levels of the statin, and increase the risk of dose-related adverse effects…

But of course the patented drugs are safe – after all, they are FDA approved, and prescribed for you by a FDA approved doctor, and sold to you at great profit by a FDA approved Pharmacy… Surely that FDA approval removes almost all the risk from these drugs, right?

Folks, I have a news flash for you: Mother Nature holds the patent on Lovastatin! Big Pharma may have figured out how to fully synthesize it in their soulless, sterile laboratories, but Mother Nature was there first!

Here is a bit of history about the “discovery” of Lovastatin taken from the on-line reference resource wikipedia: (edited for brevity – full article available at Wikipedia )

Akira Endo and Masao Kuroda of Tokyo, Japan commenced research… in 1971. The first agent isolated was mevastatin (ML-236B), a molecule produced by Penicillium citrinum. The pharmaceutical company Merck & Co. showed an interest in the Japanese research in 1976, and isolated lovastatin (mevinolin, MK803), the first commercially marketed statin, from the mold Aspergillus terreus.

But mankind has known about the properties of this Miracle of Mother Nature for thousands of years – here is an another excerpt from the on-line resource wikipedia: ( full article available at: Red Rice Yeast )

In addition to its culinary use, red yeast rice is also used in traditional Chinese herbology and traditional Chinese medicine. Its use has been documented as far back as the Tang Dynasty in China in 800 A.D. and taken internally to invigorate the body, aid in digestion, and remove “blood blockages”.

This whole silly thing just makes me want to shake my head – for it is nothing new, and the FDA has tried this several times before with Red Rice Yeast. Each time they try it, their ban crumbles under the weight of logic:

  • If Lovastatin is a unique, synthesized, patented drug, how could Mother Nature have possibly gotten there first with something as lowly as a fungus?
     
  • If Lovastatin is a new and novel thing (and therefore worthy of patent protection,) what were the ancient Chinese doing with it in 800 A.D.?
     
  • If the natural, less potent (but just as effective) substance is so very dangerous that we must be “protected” from it, how can the synthesized, isolated version be so much safer that it is sold without prescription (O.T.C or Over The Counter) in Britain, with Big Pharma agitating for the same here in the US?

To their credit, the FDA has so far resisted Big Pharma’s call – probably because they are wary of the logic that says if Big Pharma’s brands of statins can be sold O.T.C., then why shouldn’t Mother Nature’s brand also be allowed to be sold?

It will be fun to follow this one, and you can be sure that HealthBeat will keep you updated as this comedy – er, story – unfolds.

And here is a parting thought… is there not a lawyer out there somewhere who would take this case? God and God’s Agent, Mother Nature vs. Big Pharma and Big Pharma’s Agent, The FDA in a lawsuit over theft of intellectual property, plagiarism, counterfeiting, and patent infringement?

What a fun trial that might be! After all, what would happen to you or I if we reverse-engineered one of Big Pharma’s creations and sold the result for billions in profits? Would we not find ourselves in court “quicker than two shakes of a lamb’s tail?”

Learn more about Red Yeast Rice at the Wellness Club website!

We Get Letters: Comments and Questions…

Janet writes to comment:

I have just signed up for your newsletter. Thank you again!
I have personally used medicinal herbs and other natural treatments for 30 years; and now know just enough to realize how little I know! ~Janet

Dr. Myatt replies:

Hi Janet:

An ancient Arab proverb goes something like this:

There are four types of men:

The man who doesn’t know, and doesn’t know that he doesn’t know. He is a fool. Avoid him.
The man who doesn’t know, and knows that he doesn’t know. He is a student. Teach him.
The man who knows, and doesn’t know that he knows. He is asleep. Awaken him.
The man who knows, and knows that he knows. He is a teacher. Learn from him.

Knowing how little you know is the beginning of wisdom!

In Health,
Dr. Myatt

And another Janet writes:

Dear Dr. Myatt,
I have a question regarding castor oil packs.  I have read that this is a good treatment for lymphoma….Then, on another website, I read one should not use castor oil packs if there is a malignancy.  Your in put would be greatly appreciated.
Thank You, Janet

To which Dr. Myatt answers:

Hi Janet:

I use castor oil packs (COP) for everything, including every type of cancer. I have been involved in several large (unpublished) studies using castor oil packs and have never seen an adverse outcome, and I have never seen any studies which show that a COP is contraindicated in lymphoma. The only time I wouldn’t use a COP is where I wouldn’t use heat, such as in a “hot” appendix.

Please keep in mind that there are MANY other things that should be done in addition to COP’s for cancer. It is difficult for a layman to sort out what will really help because of all the conflicting stories one hears. As you probably know, “everybody is an expert” when you have cancer. The lady next door, your butcher, baker and candlestick-maker, the gal at the health food store — everybody “knows” a cure for cancer that you should be using! The trouble is, 99% of such advice is wrong.

An holistic physician can make specific recommendations based on the individual, and this is much more productive.

Here is a note (which the patient gave me permission to use ) from a Stage 4 ovarian cancer patient. I don’t know if you’re familiar with “staging,” but stage 4 is as high as it gets, and ovarian cancer is usually a death-sentence. She wrote last week after her check-up with the oncologist:

Hi Dr. Myatt –

Well, I’m home now – been a long day.  He (oncologist) gave me an internal exam as usual to see what’s growin’ – because the last time I was there (3 mo. ago) he felt stuff growing – Well, guess what – he felt NOTHING!! NADA – NIENTE – 0 growths!! – and he can’t figure it out.  So he wants to see me in 3 more months and no scans ordered.  How do you like that!
Bye!
Gail

And a note she sent out to friends the next day:

Hi Everyone – I just had another ‘cancer visit’ with my oncologist.  I was delighted with the results.
On his examination – he could not feel the cancer that was growing the last time I was there even though my cancer marker was elevated a little.  He expected me to be bloated and full of growths, but I wasn’t. He is baffled.  I attribute this as a result of working with Dr. Myatt – a nutritionist in Arizona – and sticking with her diet and and supplements.

So, to all my family and friends – Thank you for your support and prayers and kind and healthy thoughts – they are working for me. Don’t underestimate their power and yours
I love you all soooooooo much
Love and Light
Gail

Janet, Gail is not an exception. We have excellent results in achieving remissions in even our advanced cancer patients. And keep in mind that I have never met any of these people in person — this work has all been done by telephone consultation.

Please, if you need solid holistic medical advice, don’t just try and stumble around with a “do it yourself” program. Cancer is a very “worthy adversary,” and I cannot recommend highly enough that you enlist the help of myself or a trusted holistic doctor to help you with this. My telephone consultation information can be found here: Telephone Consultations

Please do keep in touch no matter what and let me know how this lymphoma case turns out. We’ll be praying for the welfare of this patient.

In Health,
Dr. Myatt

Muscular and joint pain is a very common and vexing problem that interferes with the enjoyment of life’s pleasures for most of us at some time or other. There are some excellent natural solutions to this problem – read on:

Dr. Myatt received this letter recently:

Hi!
I am a friend of a patient of yours and he mentioned that you could probably suggest a vitamin/mineral that might help my muscle soreness. Have been to a Dr. who ruled out Fibromyalgia. I am very active with work, motorcycles and horses. Have any suggestions? Thank You, Tanya N.

Hi Tanya,

Thank you for your question. Muscle soreness can result from many things, and combinations of things. The very best way to sort this out would be to arrange an
alternative medicine consultation
with Dr. Myatt – this will save you time, money, and uncertainty, and provide you with a very definitive plan for better health.

Here are some general suggestions:

An optimal dose multiple vitamin / mineral / micronutrient formula such as Maxi-Multiis a cornerstone for anyone’s good health. Without optimal nutrition, the cells of your body (including your muscles) cannot function properly.

CoEnzyme Q 10 (CoQ10) is an important energy molecule for the mitochondria (the energy units) of our body’s cells. The body produces CoQ10 naturally, but many people are deficient for a number of reasons, including prescription medication use – particularly the use of cholesterol-lowering drugs. Without adequate energy supplies your muscles cannot function at their best and may feel tired and achy. CoQ10 is also a powerful antioxidant.

Omega-3 fatty acids are essential to many processes in the body. They are anti-inflammatory. Deficiencies in Omega-3 fatty acids can contribute to a subtle body-wide inflammatory state. The Standard American Diet is woefully deficient in Omega-3 fatty acids. An excellent source is Max EPA .

Bromelainis nature’s premier anti-Inflammatory herb, useful for all types of infection, injuries, inflammation, sinusitis, cardiovascular disease, rheumatic disease, autoimmune disease, and cancer. It is very effective at reducing swelling and inflammation, thereby reducing pain and discomfort of muscle soreness.

Cox-2 Support is a new product that many of Dr. Myatt’s patients and Wellness Club members have reported excellent results with. This herbal blend was created to help support normal healthy Cox-2 levels. You are no doubt familiar with the Cox-2 inhibitor drugs such as Vioxx and Bextra and others which have earned a reputation for being  dangerous. Cox-2 support was formulated to give similar pain relief by helping the body to produce normal, healthy levels of Cox-2 compounds instead of creating artificially high levels of these compounds in the body by preventing their normal metabolism as the discredited Cox-2 inhibitor drugs are designed to do. It is well worth a try for relieving all kinds of muscular and joint discomfort.

Hope this helps,

Cheers,
Nurse Mark

We Get Letters II – Readers Ask Medical Questions…

Q.) Hello Dr. Myatt,

I would be interested in information regarding high cholesterol (my LDL is 314!!), halting or REVERSING coronary artery disease (several 40% blockages), and osteoporosis (severe—I’m trying strontium now after refusing Forteo), lowering blood pressure in a healthy way (I’m 53, 5′ tall and weigh 100 pounds on a good day!) and fibromyalgia (Yep, that too). The laundry list goes on and on, so at this point just about anything you talk about would be of interest to me or a family member!
Trying to avoid as many pharmaceuticals as possible, but have tried all the ‘naturals’, and I still haven’t found the solution….

Your site is great. I look forward to your newsletters!
Best regards, Eliz

A.) Hi Eliz:

Welcome aboard! As I’m sure you know, I can’t really respond personally to every complaint you have (I don’t have NEARLY enough information). To do so would require a telephone consultation. But there are plenty of highly informative pieces to help answer these questions on our main website ( DoctorMyatt.com ) and on this site.

This should get you going: High Cholesterol .

And be sure to see these HealthBeat articles:

And this whitepaper: (which will be pulled from the site soon and made into a white paper for purchase, so grab this while you can for free) Lower Cholesterol Naturally

See our information about Osteoporosis: and our HealthBeat article Strontium: The Missing Mineral for Osteoporosis Prevention and Reversal:

Fibromyalgia: that’s a “case by case” basis; I recommend a phone consult. And I’ll work on a general information page for this topic and post it to the main website.

There’s a problem with a “do it yourself” approach to natural health, especially when you have some serious medical concerns. You wind up buying all of the “best-hyped” supplements (and natural manufacturers can be every bit as “hypey” as Big Pharma!), waste a lot of time and money, and you still haven’t done anything specific for your case.

There’s a reason why naturopathic medical doctors spend 4 years in medical school after 4 years of pre-med. That’s because a precise understanding of the patient’s complaints, and targeted recommendations, takes a lot of knowledge and understanding. The “do it yourself” approach to medicine is, for most people, a waste of time and money and can even be dangerous. Get some professional assistance! I’m here if you need me….

P.S. to all HealthBeat News Subscribers: Remember that you’ll find a boat-load of free, no-hype holistic health information at DoctorMyatt.com.

You can also look up past articles from HealthBeat at our new HealthBeat Archives page.

All the links above were taken from our free-to-access websites.

In Health,
Dr. Myatt

Laughter is Good Medicine: Kids Say The Darndest Things – Part 2

When my grandson Billy and I entered our vacation cabin, we kept the lights off until we were inside to keep from attracting pesky insects. Still, a few fireflies followed us in. Noticing them before I did, Billy whispered, ‘It’s no use, Grandpa. The mosquitoes are coming after us with flashlights.’

When my grandson asked me how old I was, I teasingly replied, ‘I’m not sure.’ ‘Look in your underwear, Grandma,’ he advised. ‘Mine says I’m four to six.’

A second grader came home from school and said to her grandmother, ‘Grandma, guess what? We learned how to make babies today.’ The grandmother, more than a little surprised, tried to keep her cool. ‘That’s interesting,’ she said, ‘How do you make babies?’ ‘It’s simple,’ replied the girl. ‘You just change ‘y’ to ‘i’ and add ‘es’.’

‘Give me a sentence about a public servant,’ said a teacher. The small boy wrote: ‘The fireman came down the ladder pregnant.’ The teacher asked, ‘Do you know what pregnant means?’ Sure,’
said the young boy confidently. ‘It means carrying a child.’

A nursery school teacher was delivering a station wagon full of kids home one day when a fire truck zoomed past. Sitting in the front seat of the fire truck was a Dalmatian dog. The children started discussing the dog’s duties. ‘They use him to keep crowds back,’ said one youngster. ‘No,’ said another, ‘he’s just for good luck.’ A third child brought the argument to a close: ‘No, they use the dogs to find the fire hydrant.’

 

 

Diabetes (Adult Type II)

Natural Support To Prevent And Reverse This Condition

Diabetes Mellitus is a condition of abnormally high fasting blood sugar (above 126mg/dl) measured on two separate occasions.

Type I diabetes is caused by a destruction of pancreatic cells that produce insulin. It is a more serious condition, and more difficult to control, than type II.

Type II diabetes is related to Western diet and lifestyle and can almost always be controlled by diet and lifestyle changes alone.

A less recognized form of diabetes is Type 1.5 which may combine features of both Type I and Type II with some loss of endogenous insulin production as well as reduced sensitivity to available insulin. This type also responds very well to dietary and lifestyle changes and supplementation.

Uncontrolled diabetes (blood sugars that continue to go above the normal 120mg/dl) result in a four-fold increased risk of atherosclerotic heart disease and a five-fold increased risk of stroke. Diabetes also increases the risk of nerve damage leading to eye disease, peripheral neuropathy (nerve disorder), increased risk of infection, and compromised circulation sometimes resulting in gangrene. Persistent high blood sugar levels can stress and damage kidney (renal) function.

Diet And Lifestyle Recommendations

  • Diet: work with an alternative medicine physician to discover optimal diet. High carbohydrate, low calorie diets are often prescribed for diabetics, but low carbohydrate diets have been shown to work much better for most type II diabetics. A special version of the ketogenic diet — what Dr. Myatt calls “The Ketone Zone” — works fast and reliably to reverse DM. Individual guidance in diet will almost always correct Type II DM and help control Type 1.5 DM.
  • Maintain a normal weight. Overweight makes the body resistant to its own insulin. A low carbohydrate diet will reduce weight quickly and even modest weight loss helps significantly with blood sugar control.
  • Exercise regularly. Exercise improves the body’s response to insulin, decreases blood sugar levels, normalizes weight and improves circulation.
  • Drink 64 ounces of pure water daily. Adequate water intake has a wide number of health benefits and specific to diabetes these include improved blood sugar regulation and improved liver and kidney function.

Primary Support

  1. Maxi Multi: 3 caps, 3 times per day with meals. Optimal (not minimal) doses of antioxidants (ACES), B complex vitamins, magnesium, chromium, vanadium and bioflavonoids are particularly important in correcting diabetes and preventing the damage that diabetes causes. Chromium picolinate is known to help improve insulin sensitivity.
  2. Omega 3 fatty acids – any or all of these:
    Flax seed meal, 2 teaspoons per day with food
    Flax seed oil capsules: 2-4 caps, 3 times per day
    Flax seed oil: 1 tablespoon per day
    MaxiMarine O3 (Omega-3 rich fish oil): 1 cap, 2 times per day with meals. Omega 3 deficiency contributes to insulin resistance and supplementation can reverse it.
    Diabetes increases cardiovascular risk factors in part through the inflammatory action of abnormally high blood sugars. O3 fatty acids have a potent anti-inflammatory effect. The Essential Fatty Acids are SO important that the U.S. Government officially recommended in 2003 that Americans get more Omega-3 Essential Fatty Acids in their diet.
  3. Maxi Greens (Advanced Phytonutrient Formula): 3 caps, 3 times per day with meals. Bilberry, grape seed extract and ginkgo are particularly important since these potent antioxidants serve to strengthen blood vessels and protect the circulatory system.
  4. CoQ10 (50-100mg): 1 cap, 2-3 times per day with meals (target dose range: 150-400mg per day). CoQ10 is essential to mitochondrial function which can be comprimized in diabetes and should be considered a mandatory supplement for anyone taking statins fo cholesterol or by anyone with any cardiac risk factors.
  5. Increased Fiber Intake: A minimum of 20 grams of fiber daily will stabilize blood sugars and provide a host of other health benefits. Dietary fiber can be difficult to obtain in adequate amounts and most Americans get woefully little in their diet. Dr. Myatt has developed a “bread” substitute that is very low carb and very high fiber.
  6. Fiber Formula: 6-12 caps per day can be useful in maintaining a good fiber intake, especially when travelling and unable to make the “Myatt Bread” mentioned above.
  7. Berberine (200mg): I cap, 3 times per day with meals. Berberine has been found to be as effective for blood sugar control as the prescription drug metformin. Do not take both metformin and berberine – take one or the other. Do NOT stop taking metformin if it has been prescribed to you without discussing it with your doctor or other health care provider.

Additional Support

Urinary Tract Health:

  • D-mannose works by preventing bacteria from sticking to the lining of the urinary tract and not by direct antibiotic action soit does not have any of the potential for negative side-effects that antibiotics do. One teaspoon in 6 ounces of water drunk twice daily can help to prevent the urinary tract infections common in diabetics, and double that (i.e.: 4 times daily) can help to resolve urinary tract infections.

With High Cholesterol:

  • Red Yeast Rice: 2 caps, 2 times per day with meals. (Target Dose 2000 mg per day) Unlike isolated “statin” drugs, Red Rice Yeast contains a mixture of related but different statins that act synergistically. As a result, lower (and safer) doses of any one statin are taken. Red Rice Yeast has been shown to lower total cholesterol and triglycerides while raising HDL levels.
    OR
  • Berberine (200mg): I cap, 3 times per day with meals. Berberine is a potent lipid-lowering compound and also has a moderate weight loss effect.

With Neuopathy (nerve pain):

  • Acetyl-L-Carnitine: 500-1,000 mg, 2-3 times per day with meals. (Target dose range: 1,000- 2,000mg per day).Acetyl-L-Carnitine helps to restore insulin sensitivity.
  • Alpha lipoic acid: 300-1200 mg daily. Improves insulin sensitivity and reduces symptoms of neuropathy.

Since these two supplements create a powerful synergy when used together Dr. Myatt offers a high-potency supplement which combines both nutrients in a single formula. One bottle of ALA-ALC is equivalent to two bottles each of our separate ALA and ALC formulas. For those who need to take both nutrients in higher potencies, this represents asignificant savings and convenience.

  • Alpha Lipoic Acid / Acetyl L-Carnitine (ALA / ALC) One or two caps daily to improve insulin sensitivity and relieve symptoms of diabetic neuropathy. This combination also improves mitochondrial function (the “energy producing units” of the cell) is also involved in the conversion of carbohydrates to energy.

Dr. Myatt’s Comment

Diabetes leads to serious health complications. All of the problems associated with aging—-impaired circulation, decreases of hearing and eyesight, and heart disease are accelerated in uncontrolled diabetes. Fortunately, Type II diabetes is almost always controllable through diet, lifestyle, and corrective nutrients and herbs. Insulin is sometimes but rarely necessary (in instances of Type 1.5 diabetes) and may be preferable to other glucose-lowering drugs. It is important to keep blood sugar levels within a normal range, thus avoiding the multiple health risks and premature aging that diabetes causes.

I find that well over 90% of Type II diabetic patients can achieve normal-range glucose control by following a ketogenic diet and the above-listed primary support measures. If blood sugars are not dramatically improved (usually completely corrected!) after three months on this program, consult with an alternative medicine physician who can help you find the best diet and supplement program. I am available for consultation by telephone and I have an excellent success rate with type II diabetic patients.

References:

Kalman D. Chromium picolinate and type 2 diabetes. American Journal of Clinical Nutrition 2003; 78(1): 92.
http://ajcn.nutrition.org/content/78/1/192.1.full.pdf

Artemis P. Simopoulos, Dietary Omega-3 Fatty Acid Deficiency and High Fructose intake in the Development of Metabolic Syndrome Brain, Metabolic Abnormalities, and Non-Alcoholic Fatty Liver Disease. Nutrients. 2013 Aug; 5(8): 2901–2923.
Published online 2013 Jul 26. doi: 10.3390/nu5082901
PMCID: PMC3775234
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775234/

Power RA, Hulver MW, Zhang JY, Dubois J, Marchand RM, Ilkayeva O, Muoio DM, Mynatt RL.Carnitine revisited: potential use as adjunctive treatment in diabetes. Diabetologia. 2007 Apr;50(4):824-32. Epub 2007 Feb 20.
https://link.springer.com/article/10.1007%2Fs00125-007-0605-4

Ziegler D, Ametov A, Barinov A, Dyck PJ, Gurieva I, Low PA, Munzel U, Yakhno N, Raz I, Novosadova M, Maus J, Samigullin R. Oral treatment with alpha-lipoic acid improves symptomatic diabetic polyneuropathy. Diabetes Care 2006; 29(11): 2365-70.
https://www.ncbi.nlm.nih.gov/pubmed/17065669

Kavinace

Neurotransmitter Support for Anxiety and Insomnia

4-amino-3-phenylbutyric acid crosses the blood brain barrier and binds GABA-B receptors (1)
Taurine is a GABA-A agonist (2)
GABA is associated with mood and anxiousness (3)

Kavinace potentiates GABA which is one of the main inhibitory neurotransmitters. Research has shown that higher GABA levels may relieve anxiety and promote restful sleep.

Dr. Myatt’s Comment: I recommend this product to my patients who are low in GABA and my experience has shown me that it works incredibly well as a sleep aid and anti-anxiety formula for these people.

As with most nutritional supplements, do not use without physician supervision when pregnant or nursing.

Suggested Dose: 1-2 capsules at bedtime or as directed by your healthcare practitioner.
Use only before sleep.
Use caution when combined with medications that have sedative properties.

Kavinace, (60 capsules) Add to cart for price.

Enter Quantity Desired and Click “Add To Cart” Button

Supplement Facts Serving Size 2 Capsules Servings Per Container 60


Amount Per Serving *%DV

Vitamin B6 (as pyridoxal 5′-phosphate)

2 mg

100%

Prorietary Blend

Taurine and 4-amino-3-phenylbutyric acid HCl

950 mg

Other Ingredients: Microcrystalline cellulose, Vegetable capsule (HPMC, water), and Magnesium stearate (vegetable source).

Does not contain gluten, corn, soy, salt, sucrose, starch, yeast, artificial flavors or artificial colors.

† Daily Value (DV) not established.

REFERENCES

1. Lapin, I. Phenibut (beta-phenyl-GABA): a tranquilizer and nootropic drug. (2001) CNS.Drug Rev. 7(4): 471-481. https://www.ncbi.nlm.nih.gov/pubmed/11830761
2. Jia et al. Taurine is a potent activator of extrasynaptic GABA(A) receptors in the thalamus. J Neurosci. 2008 Jan 2;28(1):106-15. doi: 10.1523/JNEUROSCI.3996-07.2008. https://www.ncbi.nlm.nih.gov/pubmed/18171928
3. Allan V. Kalueff, Neurobiology of Memory and Anxiety: From Genes to Behavior. Neural Plast. 2007; 2007: 78171. Published online 2007 Jan 10. doi: 10.1155/2007/78171
PMCID: PMC1847471 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1847471/
4. Shulgina, G.I. On neurotransmitter mechanisms of reinforcement and internal inhibition. (1986) Pavlov. J.Biol.Sci. 21(4): 129-140.
5. Sulaiman SA, Suliman FE, Barghouthi S. Kinetic studies on the inhibition of GABA-T by gamma-vinyl GABA and taurine. (2003) Enzyme Inhib Med Chem 18(4): 297-301.
6. Saransaari, P. and Oja, S.S. Taurine and neural cell damage. (2000) Amino Acids 19(3-4): 509-526.

These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.