Showing posts with label fibro. Show all posts
Showing posts with label fibro. Show all posts

Tuesday, October 2, 2012

Fibromyalgia Poorly Served By Drug Happy Rheumatologists



The term “fibro” was used to designate soft (or fibrous) tissue involvement and “myalgia” is Latin for “pain”. 

Fibromyalgia was originally thought to be a rheumatologic condition because - like a disease such as rheumatoid arthritis - it is characterized by musculoskeletal pain. But research has since shown that there are no abnormalities in the musculoskeletal system in people with fibromyalgia. Instead, the problem appears to lie in the pain processing pathways of our central nervous system.

The term Fibromyalgia was created by rheumatologist Dr. Frederick Wolfe in 1984 to describe a condition affecting primarily women.

Of course if you’re subscribed to my free Health Matters newsletter, http://drmurphreesnewsletters.com, you read my article about how Dr. Wolfe now denies that fibromyalgia is a real disease-Sad but true.

Before 1990, no guidelines for evaluating and diagnosing fibromyalgia existed. To reduce misdiagnosis and confusion, the American College of Rheumatology (ACR) sponsored a multicenter study to develop these criteria; the results were published in 1990. In 1992, at the Second World Congress on Myofascial Pain and Fibromyalgia, the diagnostic criteria for fibromyalgia were expanded and refined.

Since rheumatologists were the first health specialty to promote and ratify the diagnostic criteria for fibromyalgia, they became the doctors of choice for seeing fibro patients. It didn’t matter that may at least early on had no idea what fibromyalgia was or how to treat it-unfortunately this is often the case today. Many rheumatologists won’t take any new fibro patients or are openly skeptical about the condition.

I believe rheumatologists are the worst possible doctors to manage a fibromyalgia patient’s case. 

Why? There are several reasons -

Because they deal in hard to treat autoimmune diseases, and see patients other doctors don’t want to see, Rheumatologists have a lengthy waiting list-may take 3 months to be seen.

A waiting list of patients can create a lack of empathy for the longwinded, hard to treat fibro patient who needs more than a five-minute office visit every 3 months. “Who cares if you come back I have plenty of other patients waiting in line to be seen.”

Rheumatologist are trained to use drugs, usually incredibly toxic drugs, Methotrexate, gold salts, Plaquenil, Enbrel, etc.

Here is the warning box info for Enbrel:

WARNING
SERIOUS INFECTIONS AND MALIGNANCIES
SERIOUS INFECTIONS.

Patients treated with Enbrel are at increased risk for developing serious infections that may lead to hospitalization or death.

Most patients who developed these infections were taking concomitant immunosuppressant’s such as methotrexate or corticosteroids.
Enbrel should be discontinued if a patient develops a serious infection or sepsis.

Reported infections include:

Active tuberculosis, including reactivation of latent tuberculosis. Patients with tuberculosis have frequently presented with disseminated or extrapulmonary disease. Patients should be tested for latent tuberculosis before Enbrel use and during therapy. Treatment for latent infection should be initiated prior to Enbrel use.

Invasive fungal infections, including histoplasmosis, coccidioidomycosis, candidiasis, aspergillosis, blastomycosis, and pneumocystosis. Patients with histoplasmosis or other invasive fungal infections may present with disseminated, rather than localized, disease. Antigen and antibody testing for histoplasmosis may be negative in some patients with active infection. Empiric anti-fungal therapy should be considered in patients at risk for invasive fungal infections who develop severe systemic illness.

Bacterial, viral, and other infections due to opportunistic pathogens.
The risks and benefits of treatment with Enbrel should be carefully considered prior to initiating therapy in patients with chronic or recurrent infection.

Patients should be closely monitored for the development of signs and symptoms of infection during and after treatment with Enbrel, including the possible development of tuberculosis in patients who tested negative for latent tuberculosis infection prior to initiating therapy.

MALIGNANCIES
Lymphoma and other malignancies, some fatal, have been reported in children and adolescent patients treated with TNF blockers, including Enbrel.

Scary huh?
The black box warning for Plaquenil is just as scary.

Immunosuppressive medications used by rheumatologists for autoimmune diseases are fraught with danger. That is the reason these drugs are used only by rheumatologists and not by internists, family physicians, or other medical specialists. Rheumatology is a medical specialty developed to prescribe and monitor the side effects of these high-risk medications.

The rheumatologists mentality has been conditioned over the years to continue prescribe more and stronger symptom suppressing drugs. This is a disastrous approach for fibromyalgia patients. Most fibro patients can’t tolerate drugs - they only make them worse. Drugs don’t make you healthy, they can be helpful but they don’t make you healthy. The only way to reverse fibromyalgia is to get healthy!

Using an atomic bomb like Enbrel or Plaquenil to treat fibromyalgia symptoms is not only stupid, it is incredibly dangerous!

Traditional medicine and drug therapy is a dead end for fibro patients. You can read my past blog Traditional Medicine Fails Fibro below or even better:

You can listen to my past First Tuesday of the Month Fibromyalgia Teleconference recordings here:


My fibro blog- Traditional Medicine Fails Fibromyalgia

Thursday, September 20, 2012

Stress Busting DHEA and Fibromyalgia


Adrenal fatigue is common among those battling fibromyalgia. 
 
The adrenal glands are located atop each kidney. These glands and the hormones they release allow us to be resilient to day-to-day stress. They allow us to build-up stamina to stressful situations-to rebound from daily stress or stressors.

Individuals with fibromyalgia will find that their adrenal glands have been stressed to the max. They will experience symptoms associated with adrenal fatigue including low energy, brain fog, poor immune function, anxiety, depression, poor sleep, and other stress depleting symptoms. In short they don’t handle stress very well. Because of this they will try to avoid stressful situations as much as possible. Those with severe cases will be become totally withdrawn from social situations, hibernating in their homes and avoiding stress at all costs.

Of course stress also increases their anxiety, makes their symptoms worse and causes them to have flare-ups.

Because they’ve lost their ability to handle stress if they have a day when they feel good and over do it (clean the house, paint the playroom, grocery shopping, etc.). Then they usually crash the next day. These flares are repeated over and over when a person suffers with adrenal fatigue.

Once adrenal exhaustion sets in, it’s not long before the body begins to break down. Getting “stressed out” and staying “stressed out” is the beginning of chronic illness for most, if not all, of the fibromyalgia patients I work with.

One way to repair adrenal fatigue and boost stress coping abilities is to supplement with the over the counter hormone dehydroepiandrosterone (DHEA).

DHEA

The adrenal cortex, when healthy, produces adequate levels of dehydroepiandrosterone (DHEA).


DHEA boosts:

• Energy, both mental and physical
• Sex drive
• Resistance to stress, builds tolerance and stamina to stress and stressors
• Self-defense mechanisms (immune system)
• General well being
  And helps to raise:
• Cortisol levels-our major stress coping hormone
• Overall adrenal function
• Mood
• Cellular energy
• Mental acuity
• Muscle strength
• Over all stamina


DHEA is notoriously low in my fibromyalgia patients. Chronic stress initially causes the adrenals to release extra amounts of stress hormone cortisol. Continuous stress raises cortisol to abnormally high levels. Then the adrenal glands get to where they can’t keep up with the demand for more cortisol. As the cortisol levels continue to become depleted from on going stress the body attempts to counter this by releasing more DHEA. Eventually they can’t produce enough cortisol or DHEA. This is where most of my patients find themselves in-low DHEA levels from years of stress.

Aging makes holding on to DHEA even tougher. Even in healthy individuals, DHEA levels begin to drop after the age of 30. By age 70, they are at about 20% of their peak levels.

Stress and DHEA

DHEA helps prevent the destruction of tryptophan (5HTP), which increases the production of serotonin. This helps provide added protection from chronic stress. Serotonin is one of the most important stress coping chemicals. This happy hormone increases or moods, reduces pain (increases pain threshold), and is responsible for stimulating the production of the sleep hormone melatonin. If you’ve read my book, Treating and Beating Fibromyalgia and Chronic Fatigue Syndrome, you know the importance of 5HTP and serotonin. And I spend quite a bit of time discussing the merits of DHEA for reversing anxiety and depression in my book, Treating and Beating Anxiety and Depression With OrthomolecularMedicine.

DHEA is one the most effective antianxiety therapies available and much safer than benzodiazepine drugs.

Studies continue to show low DHEA to be a biological indicator of stress, aging, and age-related diseases including neurosis, depression, peptic ulcer, IBS, and others.

DHEA and Immune Function

The decrease in DHEA levels correlates with the general decline of cell-mediated immunity and increased incidence of cancer. DHEA protects the thymus gland, a major player in immune function. DHEA is a potent immune booster. It is one of my go to supplements when treating patients with poor immune function including those with chronic fatigue syndrome and shingles.

Get Tested
DHEA Supplement I recommend to my patients

To know if you need to start taking over the counter DHEA, have your blood tested. The normal range is quite large and so most doctors will tell you if you have DHEA show up above 20 you are good. Don’t listen to this nonsense. Numerous studies and 17 years of clinical experience show that optimal levels of DHEA are needed for optimal health. For women optimal DHEA levels should be above 250 and for men closer to 350.

Thursday, September 13, 2012

You May Have A Stupid Doctor If ...



You May Have A Stupid Doctor If-
He or she tells you fibromyalgia doesn’t exist.

You May Have A Stupid Doctor If-
He or she dismisses your fibromyalgia symptoms as nothing more than you being a hypochondriac-someone wanting attention.

You May Have A Stupid Doctor If-
He or she tells you that more exercise, sleep or losing weight is all you need to do to for your fibromyalgia symptoms-you know the doctor who says “you just need to improve your sex life, take a vacation, lose some weight, your just depressed, it is just PMS…”Give me a break, this doctor doesn’t have a clue!

You May Have A Stupid Doctor If-
He or she tells you that all your blood work looks normal so you must be a “drug seeker.” It may not occur to this stupid doctor that you never mentioned you wanted pain medication, that in fact you have repeatedly declined to take pain meds in the past. What you are really seeking is to have a doctor listen, understand and help you feel better.

You May Have A Stupid Doctor If-
He or she fails to order the proper tests, especially but not limited to thyroid tests. Simply following the herd and only ordering routine tests, including “the normal” thyroid tests, stimulating hormone (TSH) and a T4 (Thyroxine) is similar to trying to critique The Sound of Music after only watching the first 20 minutes of the movie/play. Your synopsis is-Julie Andrews was a quirky nun. Ok, what about the Captain, his children, the Nazi party, the wedding, and the escape? My point is stupid doctors are happy to stay stupid. They don’t care to practice the art of doctoring, being a detective, investigating anything outside the routine.

They’re happy to follow the herd, not make any waves and dispatch the drugs the pharmaceutical rep asks them to based on “this is how we’ve always done it.”


Sorry but it burns me up that patients go to their doctor with all the symptoms of low thyroid-fatigue, depression, anxiety, elevated cholesterol, brain fog, weight gain, cold hands, cold feet, swelling, tingling pains, constipation, hair loss-only to be told their blood work looks fine.

They totally miss the diagnosis because they don’t go the extra mile (“this is how we’ve always done it”). They are then only too happy to promote life draining drugs to cover up the hypothyroid symptoms-Ritalin for low energy, Lipitor for elevated cholesterol, Zoloft for depression, Lyrica for tingling pain…it just goes on and on.

The patient’s symptoms and poor health continue to grow year after year when all the stupid doctor needed to do was run the right tests, or think outside the box and recommend prescription or over the counter thyroid hormone therapy. Correct the cause, low thyroid and all the symptoms go away!

You May Have A Stupid Doctor If-
He or she dismisses the very real condition known as adrenal fatigue. Adrenal fatigue occurs when your stress coping glands, the adrenals become to stressed to perform properly. Stress is definitely the catalyst for disease! They will tell you your symptoms associated with adrenal fatigue, low energy, brain fog, low immune function, depression, poor sleep, weight gain, etc. are from getting older or all in your head.

Why? Because doctors are evaluating blood work for disease not function. They don’t care that your adrenals aren’t functioning at optimal levels (to allow you to deal with and rebound from stress). They only care if you have TOTAL adrenal failure, Addison’s disease. Blood tests won’t show adrenal fatigue but a four-sample, 16-hour saliva test will.

Guess what else stupid doctors don’t believe in, saliva tests. This despite they’ve been proven valid and are recognized by insurance companies, accredited labs, Harvard Medical School, and other leading organizations.

You May Have A Stupid Doctor If-
He or she has you taking two different SSRI or SSNRI antidepressant medications. These drugs, including Savella, Cymbalta, Effexor, Celexa, Zoloft, Paxil, Pristiq, and Prozac are supposed to help your brain re-uptake the happy hormones serotonin and or norepinephrine. It makes no sense to be on more than one of these drugs at the same time-you only increase the risk of more side effects (including poor sleep, depression, anxiety, muscle pain, etc.).

If you stop to get gas why would you mix 89% with 91% unleaded fuel? You wouldn’t. If you need more fuel you simply increase the cars intake, you don’t mix them. Mixing these drugs is a sign of a lazy and stupid doctor!

You May Have A Stupid Doctor If-
He or she has you taking a stimulant drug or drugs and a relaxant or tranquilizing drug. Examples include-taking Ritalin, Adderall, Strattera, Intuniv, Vyvanse, Wellbutren, Effexor, Cymbalta, Savella, or Pristiq and a benzodiazepine drug for anxiety including Ativan, Xanax, Seroquel, Klonpin, Valium or Busbar. One drug is revving you up the other is making you a zombie.

Lazy or stupid doctors are happy to over medicate you. They don’t take time to study how to naturally reduce your anxiety, which after the fact, you can and should use natural amino acids (which make the happy, calming and or stimulating brain hormones, serotonin and norepinephrine)-no one has a drug deficiency!

You May Have A Stupid Doctor If-
He or she has you taking a potentially stimulating drug while you are complaining of insomnia. It used to surprise me to see doctors recommending their patients take a SSRI or SSNRI at bedtime. Why? Because these drugs can, not only re-uptake the calming hormone serotonin, they can also re-uptake the stimulating hormone adrenaline. Now I may not be “a real doctor,” I’m only a little chiropractor nutritionist, but I know enough about biochemistry and physiology and after 17 years experience of treating fibro I know you don’t do anything to potentially sabotage deep restorative sleep.

Timed-release stimulant drugs including some antidepressants and Ritalin are notorious for causing sleep disorders. AND you should know that these drugs deplete your natural sleep hormone melatonin.
Stupid, stupid, stupid.

But I’m sure the stupid doctor simply increased your sleep medication or added another potentially dangerous drug to knock you out at night.

Well I could go on and on about stupid doctors but I’ve got to finish up now so I can pack my clothes for my weekend seminar on Functional Medicine. I’ll be learning about more tests that stupid doctors don’t use or even know about. I’m happy not to follow the herd, and strive to be a smart doctor, even though I’m still learning how to work the new TV remote.

Wednesday, February 29, 2012

If You Have Fibromyalgia or CFS-Avoid NutraSweet


The Health Dangers of NutraSweet-Fibromyalgia and Aspartame

Aspartame can be found in most diet sodas and in other artificially sweetened food products. Commonly known as NutraSweet or Equal, it is broken down by the body into methanol and formaldehyde. 
Toxic levels of methanol are linked to systemic lupus and now Alzheimer’s disease. 

Methanol toxicity can cause depression, brain fog, mood changes, insomnia, seizures, and similar symptoms associated with multiple sclerosis. 

As for formaldehyde, it is grouped into the same class of drugs as cyanide and arsenic.

An EPA assessment of methanol states that methanol "is considered a cumulative poison due to the low rate of excretion once it is absorbed. In the body, methanol is oxidized to formaldehyde and formic acid; both of these metabolites are toxic." They recommend a limit of consumption of 7.8 mg/day. A one-liter (approx. 1 quart) aspartame-sweetened beverage contains about 56 mg of methanol. Heavy users of aspartame-containing products consume as much as 250 mg of methanol daily or 32 times the EPA limit.

When the temperature of aspartame exceeds 86 degrees F, the wood alcohol in the product is turned into formaldehyde and then into formic acid. Formic acid is the poison contained in the sting of a fire ant.
There are over 92 documented symptoms from the use of aspartame.

Aspartame accounts for over 75 percent of the adverse reactions to food additives reported to the FDA. Many of these reactions are very serious including seizures and death. A few of the 90 different documented symptoms listed in the report as being caused by aspartame include: Headaches/migraines, dizziness, seizures, nausea, numbness, muscle spasms, weight gain, rashes, depression, fatigue, irritability, tachycardia, insomnia, vision problems, hearing loss, heart palpitations, breathing difficulties, anxiety attacks, slurred speech, loss of taste, tinnitus, vertigo, memory loss, and joint pain.

Could Aspartame be contributing to your fibromyalgia or CFS symptoms?

One common complaint of persons suffering from the effect of aspartame is memory loss. Ironically, in 1987, G.D. Searle, the manufacturer of aspartame, undertook a search for a drug to combat memory loss caused by excitatory amino acid damage.

One expert, Dr. Olney, a professor in the department of psychiatry, School of Medicine, Washington University, a neuroscientist and researcher, and one of the world's foremost authorities on excitotoxins. (He informed Searle in 1971 that aspartic acid caused holes in the brains of mice.)

For more information about the dangers ofAspartame see Aspartame Sweetpoison, written by author Dr. Janet Starr Hull.

Saturday, March 12, 2011

Do You Have Fibromyalgia or Chronic Fatigue Syndrome or Both


Chronic Fatigue Syndrome (CFS) shares many similarities with FMS. Several studies have suggested that they are the same illness. One study comparing 50 CFS patients with 50 FMS patients showed the following symptoms to be the same for both groups: low-grade fever (28%), swollen lymph nodes (33%), rash (47%), cough (40%), and recurrent sore throat (54%). Another study comparing CFS patients with FMS patients showed that brain wave patterns, tender points, pain, and fatigue were virtually identical in both groups.

A 1997 study by Allen N. Tyler, MD, ND, DC, muddies the water even further. Ten patients, all of whom met the ACR criteria for FMS, were selected at random for blood testing. They were tested for influenza type-B antibodies, and three of the ten tested positive. Another randomly selected group of ten FMS patients (meeting all the ACR criteria) were tested for antibodies to influenza type-A. Nine of them tested positive.

Symptoms of CFS include-
mild fever
fatigue
recurrent sore throat
painful lymph nodes
muscle weakness
muscle pain
migratory joint pain
prolonged fatigue after exercise
recurrent headaches
neurological or psychological complaints, such as:
depression
excessive irritability
forgetfulness
sensitivity to bright light
confusion
inability to concentrate
sleep disturbances


Due to weakened immunity, individuals with chronic fatigue have terrible problems with energy as well as recurring bouts with the flu, colds, sinusitis, and other immune problems. As with so many complex chronic illnesses, CFS may be aggravated by a wide variety of environmental and physiological challenges. Food allergies, environmental sensitivities (odors), heavy metal toxicity (mercury, aluminum, etc.), yeast overgrowth, parasites, and vitamin/mineral deficiencies can all contribute to CFS.

All of us have been exposed to mono or the Epstein-Barr virus (or other viruses) at one time or another (usually as teenagers), but our bodies are usually strong enough to overcome the exposure. We develop immunity to the virus. We carry the virus around inside of us until we die. Normally, this dormant virus never causes any more problems. It is kept in check by a healthy immune system.
Individuals with CFS aren’t able to squelch the normally dormant virus (or other bug), and it begins to raise its ugly head once again. Individuals with CFS may feel like they are walking around with the “flu from hell.” They have all the symptoms of a very bad case of the flu. But unlike most cases of the flu, CFS doesn’t disappear after one or two weeks.

HOW TO QUICKLY DISTINGUISH BETWEEN FMS AND CFS
A positive EBV panel is a clear indicator that someone has CFS. However, you don’t need a blood test to diagnose CFS. If you have chronic fatigue (hard to get out of bed each day), achy diffuse pain, chronic sore throats, and a lowered immune function (chronic infections), then you either have CFS or you’re at high risk of developing it.

The CFS patient usually has chronic infections (sinusitis, upper respiratory, urinary tract infections colds, flu, etc.) and is sick several times a year. He or she gets at least two bad infections a year. They will usually have chronic or intermittent sore throats, swollen lymph nodes, and periodic fevers. They usually ache all over. FMS patients may ache all over as well, but they usually have specific areas (neck, low back, etc.) that are the most troublesome.

Many CFS patients will also have a sluggish liver (more likely than in those with FMS). Clues that would lead you to suspect a sluggish liver include funny or negative reactions to medications (they take something to put them to sleep, and it wakes them up, or “a little goes a long way”); intolerance to caffeine, alcohol, or odors (the longer they’ve had the illness, the more sensitive they become to odors, perfumes, gasoline, smoke, cleaners, etc.); and a history of elevated liver enzymes on past blood work. Of course, anyone with hepatitis or fatty liver has a sluggish liver. Long-term prescription-medication therapies can also create a sluggish liver.

CFS AND LIVER DYSFUNCTION
CFS patients are more likely than FMS patients to have a sluggish liver. Clues that would lead you to suspect you may have a sluggish liver include:
chemical sensitivities (see below)
funny or negative reactions to medications (you take something to put you to sleep but it wakes you up, or a little goes a long way)
intolerance of caffeine
intolerance of alcohol
intolerance of odors (the longer patients have had the illness, the more sensitive they become to odors, perfumes, gasoline, smoke, cleaners, etc.)
a history of elevated liver enzymes on past blood work.

CFS patients may have severe chemical sensitivities and may not be able to tolerate nutritional supplements. They may have allergic reactions to even the purest multivitamins. This complicates things. It is best to start slow, especially with individuals who have severe chemical sensitivities.

Individuals with fibromyalgia have a lot of similar symptoms of CFS but in general their immune system is not compromised-they don’t get chronic sore throats, and infections. A person can be a true fibromyalgia patient-poor sleep, chronic pain, etc. but intact immune function or a true CFS patient fatigue, achy pain, and KEY poor immune function. However patients can share symptoms of both of these illnesses and have both.
You can read more about fibromyalgia and CFS on my website www.treatingandbeating.com

Friday, March 4, 2011

Fibromyagia-Stress Coping Savings Account


We’re all born with a stress-coping “savings account” filled with chemicals—such as hormones, amino acids, and nutrients—that can be deposited and then withdrawn when needed. Depending on our genes, some of us have large accounts, and some of us have smaller ones. The more stress we’re under, the more withdrawals
We make. If we make more withdrawals than deposits, we get overdrawn, and poor health quickly follows. Individuals with fibromyalgia and/or CFS have bankrupted their stress-coping savings account.
Although some patients bankrupt their accounts with one overwhelming event, most experience a series of stressful events over the years. These events typically involve stressful jobs, marriages, family dynamics, surgeries, illnesses, loss of a loved one, divorce, financial failure, etc.

Many of my patients can remember the day when their account went belly-up. It might have been after a surgery or following the loss of a parent. Whatever happened, the person was never the same from that point on; she just couldn’t get well. My CFS patients often relate how they came down with a bad case of flu and just never completely got over it. Once these individuals get enough rest and stop making withdrawals, they may attempt to do something as mundane as sweep the kitchen floor only to be wiped out once again. And forget about grocery shopping! 
That could put them in bed for weeks.

FMS and CFS are the result of internal biochemical (hormonal, enzymatic, neuronal, and chemical) imbalances that manifest themselves as physical symptoms (pain, weakness, and mental impairment). So in order to right the homeostatic system, you must correct the underlying biochemical problems. Just like an onion, you peel away one layer at a time until you get to the core. But we’ll discuss these practical steps soon. For now, let’s make sure that you understand all of these “layers of the onion.” One of these is dysautonomia.


Dysautonomia is defined by Taber’s Cyclopedic Medical Dictionary as “a rare hereditary disease involving the autonomic nervous system with mental retardation, motor in coordination, vomiting, frequent infections, and convulsions.” But dysautonomia symptoms are usually nowhere near this severe. Dysautonomia patients are more likely to be suffering from mitral valve prolapse and neurally mediated hypotension (dizziness upon standing) than mental retardation and vomiting.

A better description, then, of dysautonomia would be a malfunction in the body’s master regulating (homeostasis) system, which—as you may recall from earlier chapters—is known as the autonomic nervous system or the HPA axis. The HPA axis (comprised of the hypothalamus, the pituitary gland, and the adrenal glands) controls millions of involuntary actions such as breathing, releasing of endocrine hormones, blood flow, smooth muscle tone, immune response, heartbeat, detoxification, and elimination. We don’t have to think about breathing; we just do it. We don’t try to pump blood through the heart and into the muscles; it is initiated and monitored by our HPA axis.

Normally all the systems in the body speak to and coordinate with one another. This is the essence of homeostasis. But when a person depletes her savings account of stress-coping chemicals, her HPA axis begins to self-destruct. This is dysautonomia. It’s as if the immune system starts to speak in Spanish, the endocrine system in German, the musculoskeletal system in Greek, and the digestive system in French! And when no one can communicate, chaos results!


Most of us can handle the ups and downs of our daily lives, even the occasional catastrophe. We dig in our heels, persevere, and eventually learn to cope. However, some individuals have an altered stress-coping system, which prevents them from managing daily stress. Human studies suggest that for some folks, the cumulative effects of physical, mental, chemical, or emotional burdens in early childhood may increase the affects of stress later in life. (It’s possible that the reason for his effect is an overstimulation or dysfunction of the HPA-axis). Retrospective studies show that the stress of emotional, physical, or sexual abuse during childhood also increases the future risk of developing certain symptoms, including many associated with FMS and CFS.

Apparently, for some children and adolescents, too many traumatic or stressful events decondition their normal homeostatic stress-coping abilities. Thus stress, particularly traumatic stress, early in life may alter the set point of their stress-response system. As they get older, have more responsibilities, and experience an increase in their daily stress, they often find their health beginning to suffer. They may start to have bouts of anxiety and depression, or perhaps they’re just tired all the time. They become extremely vulnerable to major stressors: the death of a loved one, chronic illness, invasive surgery, physical trauma, etc. Like a ticking time bomb, it’s only a matter of time before they explode.
This is especially true for those who have a genetic predisposition that makes them more susceptible to the ill effects of daily stress, including reduced serotonin levels. Some research has suggested that FMS/CFS patients may in fact by afflicted by this genetic abnormality.

Sadly, I find that many of my FMS and CFS patients have experienced physical, emotional, or sexual abuse as a child. Some patients report abuse from their spouse (sometimes physical but more often emotional). This stressful situation, though begun in adulthood, can still eventually deplete their stress-coping chemicals and lead to a state of disease.

The symptoms of fatigue, pain, poor sleep, poor digestion, irregular bowel movements, mental confusion, poor memory, anxiety, and depression are all warning signs that certain stress-coping chemicals (including vitamins, minerals, amino acids, essential fatty acids, and hormones) have become deficient. These deficiencies then complicate one another until the body’s homeostatic mechanism and 

HPA-axis become dysfunctional.
The final tick of the time bomb may be just another part of chronic daily stress, or it may be a sudden traumatic event like the birth of a new baby. I know I didn’t think I’d survive the first colic-plagued six months of my daughter’s life. And I’m extremely healthy! I pulled my weight and spent every other night walking and rocking my crying daughter into the early morning, and this is main reason it took another nine years before my wife could convince me to have another child!

It’s no wonder that many of my patients report that their fibromyalgia began after the birth of a child, often a firstborn. Anyone with children can relate to sleeping (if you can call it that) with one eye and two ears open, making sure the baby is breathing. Or how about trying to sleep without moving so that you don’t wake the baby up? Then there’s the endless nights of breast and bottle feedings, diaper changes at two in the morning, and the early morning piercing cry: “I’m awake, folks!” It’s enough to bankrupt anyone’s stress-coping savings account! Whew! Let’s move on.
we are all born with a stress-coping savings account filled up with chemicals we need for the body to work properly. These chemicals—serotonin, dopamine, norepinephrine, cortisol, DHEA, HGH, and others—help us deal with stress.

Every time we are exposed to stress (chemically, emotionally, mentally, or physically), we make withdrawals from our stress-coping savings account. These withdrawals can be triggered by any stimulus, including sounds (especially loud or irritating noise), odors, and bright light. You may have noticed that the longer you’ve had your illness, the less tolerant you are to certain odors, chemicals, or noises.

Emotionally stressful situations cause the body to release adrenaline, cortisol, and insulin, and these stress hormones stimulate the brain to secrete serotonin. Long-term stress and poor dietary habits can therefore deplete the body’s serotonin stores. If we aren’t careful we’ll find that we are making more withdrawals than deposits, bankrupting our own account. And when we do, FMS and CFS are often the result.

But when a person enters deep, restorative sleep, she makes more serotonin, which then gets deposited into her stress-coping savings account. The more stress a person is under, the more serotonin she’ll need to replenish. It’s a vicious cycle. If she doesn’t have enough serotonin, she won’t be able to go into the stage of sleep in which she is able to make more serotonin!
solving your serotonin problem

The first reaction of many physicians to a patient’s serotonin deficiency is to recommend a selective serotonin reuptake inhibitor (SSRI) drug. But while prescription antidepressants can be helpful, they have some serious potential side effects (see chapter 6). In addition, they tend not to work for FMS patients. And here’s why: SSRIs can help a patient hang onto and use their naturally occurring stores of serotonin. They work like a gasoline additive would work in your car, helping to increase the efficiency of “fuel.” But most of the patients I see with fibromyalgia are running on fumes! A gasoline additive is not likely to help. If you don’t have any serotonin to re-uptake, then using a serotonin re-uptake inhibitor drug is pointless.

And by pointless, I mean exactly that. It’s money thrown away. In fact, depending on which study you quote, from 19% to 70% of those taking antidepressant medications would do just as well on a placebo. 
This is precisely why I recommend that my fibromyalgia patients boost their serotonin levels by taking 5-HTP, not an antidepressant. Why put an additive in your gas tank...when you can just fill it up with what it’s really thirsty for? The proper function of our adrenal glands is second only to a good night’s sleep in winning the battle against fibromyalgia and chronic fatigue syndrome.

The importance of restoring optimal adrenal gland function can’t be overstated. An individual with FMS or CFS who suffers from adrenal fatigue will find her stress-coping abilities to be severely depleted. Simply put, she “stresses out” easily. Consequently, she has to avoid stressful situations in order to just feel OK (which makes for complicated relationships). Stress causes her physical pain, worsens her other symptoms, and can cause a flare-up that lasts well beyond the time of the stressful incident.
If she has a day when she feel good, she’ll usually overdo it. Her reason? “I’ve got so much to do! And who knows when I’ll feel good again.” So she cleans the house, stays late at work, re-sods the front yard, goes Christmas shopping, and plays outside with the kids. Then she crashes—hard—the next day. 

She just doesn’t have any resistance to stress. If her sister calls at 9:00 p.m. with some bad news, she can just forget about sleeping. And of course she’ll feel terrible the next day, so she can go ahead and cancel that lunch date. “But how can I cancel on my friend again? She already thinks I’m avoiding her!” She just can’t make any firm plans, because she never knows if she’ll be having a good or bad day. Below are some sample accounts from patients of mine who have suffered from adrenal fatigue. Does any of it sound familiar?

Adrenal fatigue is already known to cause many of the same problems associated with CFS/FMS, such as muscle or joint pain, dizziness, fatigue, decreased mental acuity, low body temperature, a compromised immune system, depression, constipation, diarrhea, and abdominal pain.

For the past 14 years, I’ve successfully treated thousands of patients with high does of certain vitamins, minerals, amino acids, and other nutrients—an approach known as orthomolecular medicine (see ch. 7). It’s based solely on biochemistry, using the right chemicals inherently natural to your body’s optimal functioning.

In short, by using the natural building blocks that make up your normal biochemistry, we can correct, drastically improve, or even reverse the cause of your illness. Nutrients— including vitamins, minerals, and amino acids—make the hormones that regulate your body. They compose every essential chemical in the body, including thyroid hormone, testosterone, estrogen, neurotransmitters (serotonin, norepinephrine, etc.), antibodies, adrenaline, cortisol, and white blood cells.

Unlike with drug therapy, there is never any danger in getting healthy. Once you become familiar with my protocols, you’ll realize that they’re safer and often more effective than drug therapy alone. And they often work quickly, having a person feel better than she has in years.

I’ve found that it’s best to start with the following core nutrients, which I call the Jump-Start Package. The supplements in this package are essential for reversing fibromyalgia and CFS symptoms, and they don’t take a lot of measuring, counting, or reorganizing of your medicine cabinet. Ninety-nine percent of the time, I start my pain-and-fatigue patients on the four pillars of the Jump-Start Program from day one: 5-HTP, adrenal cortex, digestive enzymes, and an optimal daily dose multivitamin and mineral formula.

When my patients begin the jump-start package, they consistently report feeling better within 2–4 weeks. 
That’s because these supplements help address the core issues of fibromyalgia and CFS. I call these the four pillars, and we begin them all at the same time.
1. 5-htp
This builds serotonin and promotes deep restorative sleep, the most important step in beating fibromyalgia and CFS. See chapter 10 to read all about it, including what to do if it doesn’t seem to be working for you.

2. Adrenal cortex
Once you get sleeping well and restore you serotonin levels, you should start feeling better than you have in years. However, if you don’t repair your sluggish adrenal glands, you’ll crash every time you attempt to overdo it. I know you can relate to having a day or two when you feel good and then overtaxing yourself only to “flare up” again and end up in bed for several days. Supplementing with adrenal cortex (500 mg. daily divided into two doses) and/or other supplements that help the adrenal gland repair itself is a crucial step towards avoiding these flare-ups. Check out chapter 11 again if you’re not convinced.

3. Digestive enzymes
The majority of my patients are suffering from poor digestion, and most are taking antacids or proton-pump inhibiting medicines to block their stomach acids. As I’ve already discussed, this can cause further nutritional deficiencies. If you’re not breaking down and assimilating the nutrients in your foods or the supplements your taking, you’ll be wasting your money and never feel as good as you could. That’s why I recommend that all of my patients take an 8X pancreatic digestive enzyme—or betaine HCl with pepsin enzyme—with each meal. Read more in chapter 12.

4. The CFS/Fibro formula
I’ve already established the important roles vitamins, minerals, essential fatty acids, and amino acids play in reversing many of the most troubling symptoms of fibromyalgia and CFS. After working with fibromyalgia and CFS patients for over a decade, I’m firmly convinced that without taking a good optimal daily allowance multivitamin-and-mineral formula similar to the one I’ve developed, patients are doomed to a life-long battle with poor health. Chapters 26–29 will give you more details about the ingredients in the CFS/Fibro Formula.

The CFS/Fibro Formula is taken as one pack with food, twice a day. I’ve designed what I consider to be (and which has proved itself to be) the best on the market, if I do say so myself.
get jumping

This Jump-Start Package is the place to begin in your journey to wellness. Start here, and give yourself some time to improve. As your stress-coping savings account builds up for a couple of weeks, you should definitely feel better. Some of you will show a dramatic improvement. You won’t be totally well yet, and you might never feel like you did when you were 20. But you shouldn’t have to suffer like you have been.

Monday, February 28, 2011

Stress and Fibromyalgia



A survey by The Fibromyalgia Network reports that 62% of their respondents list physical or emotional stress as the initiating factor in their acquiring fibromyalgia.
I believe chronic stress is the underlying catalyst for the onset of HPA dysfunction and fibromyalgia. Several studies have demonstrated how chronic stress undermines the normal hypothalamic-pituitary-adrenal axis (HPA) function.
When explaining the role of stress in fibromyalgia, I find the following analogy helps put stress and fibromyalgia into perspective.

“We are all born with a stress coping savings account. This account is filled with numerous chemicals we use to help us deal with daily stress-serotonin, norepinephrine, cortisol, magnesium, and other important hormones and nutrients al help counter stress. The more stress we encounter, the more stress coping chemicals we use. We replenish our stress coping savings account with adequate rest. Consistent deep restorative sleep ensures we are making more deposits than withdrawals from our stress coping account.

Since fibromyalgia patients struggle with getting a consistent good nights sleep they eventually bankrupt their stress coping account. Once tyour stress coping savings account is depleted poor health and the many symptoms associated with fibromyalgia, pain, fatigue, brain fog, anxiety, depression, low thyroid, etc. start to raise their ugly heads.

With so many different symptoms, it’s no surprise that fibromyalgia and CFS patients are typically taking 6–12 different prescription drugs. Lyrica, Elavil, Klonopin, Paxil, Effexor, Xanax, Trazadone, Neurontin, Zanaflex, Ambien, Lunesta, Cymbalta,  and Provigil have all been heralded as “the drug” for fibromyalgia. Some of these are helpful, some worthless, and some really dangerous.

Drug management alone typically fails to yield lasting relief from the most common fibromyalgia and CFS symptoms, and patients’ and doctors’ optimism over a new drug treatment eventually gives way to this sad reality. Oh well, a new drug with an even larger marketing budget is on the horizon. (Forgive my cynicism. I’ve just seen this situation so many times!)

After seventeen years of specializing in treating and beating fibromyalgia I’ve learned that traditional medicine alone yields little if any long-term results.
The best hope for those with fibromyalgia is to find and work with a doctor who practices integrative medicine-combining judicious use of prescription drugs (short-term if possible) and natural therapies (vitamins, minerals, and other nutrients).

Combining prescription drugs (when needed) with natural supplements allows the symptoms associated with fibromyalgia to be corrected, not just covered-up.
Hang in there-you can beat fibromyalgia. Don’t give up.


Friday, February 25, 2011

Here We Go Again-Another Idiot Doctor

I was just made aware of a story on fibromyalgia that The New York Times ran early last year. How many arrogant idiotic doctors are there in this world. Just when I feel like patients with fibromyalgia are finally getting the support and understanding they deserve, some prehistoric physician, locked in the dark ages, paints fibromyalgia with the "all in their head" label. It would be funny if it weren't so offensive to those who battle this illness on a daily basis. Fibromyalgia is a real disease and those with  the syndrome suffer real pain. Who would want to make all this up in their head?


Here is a partial snippet of the article


The Voices of Fibromyalgia


People who suffer from fibromyalgia experience problems beyond the pain caused by their illness. Their condition is little understood and hard to explain, and often they are disbelieved by doctors. Even friends and loved ones may express skepticism toward the fibromyalgia sufferer, who, burdened with inexplicable pain, may cancel social plans, miss work and recoil from physical affection because it hurts too much.
For a glimpse into the frustrating world of fibromyalgia sufferers, listen to the latest installment in the Patient Voices series by producer Karen Barrow.
You’ll meet Christine Wysocki, 33, of St. Augustine, Fla. who waited three years before a close friend and co-worker believed she had a health problem.
“Frankly I still don’t know if I understand exactly what it is,” says Ms. Wysocki. “Everything seems so vague about what fibromyalgia is, and it feels like no one wants to commit to what an actual answer is.”
And there’s Leon Collins, 59, of Clayton, N.J., who was relieved when he heard he had fibromyalgia because he at least had a diagnosis after many other doctors had dismissed his symptoms.
“We even experienced one doctor who wanted to send me to a psychiatrist because he felt my pain was imagined,” he said.

The Skeptic 

Count me as one of the skeptics. Not necessarily whether fibromyalgia exists, just that the vast majority of sufferers actually have it. I won’t use the word hypochondria, because I think that is inadequate. I think that many of these people suffer from a somatiform or somatization disorder. Still a disorder in need of treatment, but not fibromyalgia.
Understand, I think that this has definitely had a “wolf-crying” effect on people who do have it, and also on people who suffer, quite beyond their control, from untreated somatiform disorders. This results, not from the inability of medical science to test and confirm the diagnoses of fibromyalgia beyond cataloging the symptom complaints of sufferers, but from the fact that so many people who report these symptoms also complan of other vague maladies and bring to doctors their own self-diagnoses that the doctors have little choice but to attempt to treat them as they are reported.
This is how I put it to the last such person I spoke to: “What are the odds, mathematically, that one person should suffer from so many obscure and medically unconfirmable maladies? Maladies that have symptoms that can only be accepted or rejected based on your word that they exist?” The simple mathematical improbability that one person suffer from Meniere’s Disease, Epstein-Barr Syndrome, and Fibromyalgia, all three vague disorders that seem to show up in varied combinations among middle aged women, commonly with a history of childhood abuse, begs the question: Why are doctors being guilt-tripped into rejecting the possibility that these patients don’t suffer from what they think they suffer from, but indeed do suffer from something? Is the mere social stigma of psychological and emotional disorders enough that we should reject the possibility? I say no.
— Dr Hirschberg

Dr. Hirscberg validates that there are stupid doctors in this world and you should avoid them like the plague. If you have a skeptic for a doctor, if he or she isn't listening to you FIRE THEM and get another doctor! 

Wednesday, February 9, 2011

Should You Take a Daily Aspirin?



What About Aspirin?
The logic behind using aspirin is based on the idea that it inhibits the formation of blood clots. It does this by preventing the production of cyclooxygenase, an enzyme responsible for making prostaglandins. Prostaglandins are hormones that perform various bodily functions. Some prostaglandins cause platelets to become stickier and adhere to one another while attaching to arterial walls. However, other prostaglandins help prevent the platelets from attaching to one another. Thus, aspirin prevents the body’s own natural self-regulating mechanisms.

This is similar to what happens when taking non-steroidal, anti-inflammatory drugs (NSAIDS). By the way, aspirin is the original NSAID. It reduces inflammation by blocking prostaglandins 1, 2, and 3. The problem with this is that prostaglandins 1 and 3 are the body’s own natural anti-inflammatory hormones. Blocking prostaglandins 1 and 3 prevents the body from releasing its own natural pain blocking chemicals.
Vioxx and Other NSAIDS Pulled from Market
Merck pulled the drug Vioxx off the market because a long-term clinical trial showed that some patients, after taking the drug for 18 months, developed serious heart problems. The data that ultimately persuaded the company to withdraw the drug indicated 15 cases of heart attack, stroke, or blood clots per thousand people each year over three years, compared with 7.5 such events per thousand patients taking a placebo.
Internal memos show disagreement within the FDA over a study by one of its own scientists, Dr. David Graham, who estimated Vioxx had been associated with more than 27,000 heart attacks or deaths linked to cardiac problems.
Studies have shown Vioxx users had twice the number of heart attacks as those taking Naproxen. These new drugs, which block COX-2 enzymes, may promote excessive blood clot formation. It appears that COX-2 enzymes counteract some of the effects of COX-1 enzymes, which narrow the blood vessels. This narrowing then causes blood to be more likely to clot.
A person taking NSAIDS, including aspirin, is seven times more likely to be hospitalized for gastrointestinal adverse affects. The FDA estimates that 200,000 cases of gastric bleeding occur annually, and that this leads to 10,000 to 20,000 deaths each year.
NSAIDs can cause high blood pressure. In one study, 41% of those who had recently started on medication to lower their blood pressure were also taking NSAIDs. NSAIDs more than double a person’s risk of developing high blood pressure.

Why isn’t my doctor telling me these things?

Good question. Most doctors and the public at large has been brainwashed into believing that these drugs pose little harm. As you’re now finding out nothing could be further from the truth.

You won’t find this behind the scenes, undercover reporting in the typical brochures on high blood pressure.

These pamphlets are by the way written by the drug companies, who of course don’t won’t you know just how dangerous their drugs are.

There have been several studies which have looked at the role aspirin may play in reducing heart attacks. But one in particular, The Aspirin Component of the Ongoing Physicians’ Health Study, is cited by physician groups, the media, and of course the drug companies who make aspirin.
This study involved 22,071 male physicians. Half of the study participants took Bufferin and half took a placebo. The study shows that over a 4.8-year period, there were 44 deaths in the Bufferin group and 44 deaths in the placebo group.
The Bufferin group did have fewer heart attacks (139 compared to 239) than the placebo group. Looking at the numbers above, we would conclude that taking Bufferin prevented 100 heart attacks. However, if we look at these numbers a little closer, you may not want to take a daily aspirin.
If we take the 11,037 who took Bufferin and divide by 100 (the number who benefited from taking Bufferin) we see that .906% of those taking Bufferin benefited. This is of course less than one percent, a number not worth the fanfare it has received.

The researchers reported that those taking Bufferin had between a 44 and 47% reduction in heart attack risk. How did they get this number? They took the 100 people who presumably didn’t experience a heart attack because of taking Bufferin and divided it by the 239 who didn’t take Bufferin and had a heart attack. This turns out to be 44%.
Researchers can do wonders with statistical analysis!
An interesting finding that somehow wasn’t revealed by this now famous study was that those taking Bufferin had a higher incidence of stroke (119), than those in the placebo group (98). Conventional doctors advocate the use of aspirin for the prevention of stroke. If we were to use the same statistical parameters by the authors of this study, we’d see that those taking Bufferin had a 21.4% increase in strokes!
Other studies that have evaluated the effectiveness of aspirin to prevent cardiovascular deaths have shown no benefit at all.  A 1975 study involving one million American men and women showed there was no benefit in taking aspirin.

The National Heart, Lung, and Blood Institute evaluated the effects of taking aspirin in a group of 4,524 participants. Half took aspirin and half took a placebo. The group who took aspirin had a 14.1% increase in heart attacks, while those taking a placebo had a 14.8% increase.
In 2003, a study linking low dose aspirin use among elderly patients caused decreased kidney function.
An Aspirin a day may not be in  your best interest after all.