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Fibromyalgia syndrome
(FMS) is an increasingly common, chronic pain disorder characterized by widespread musculoskeletal aches, stiffness and general fatigue.
The term "fibromyalgia," meaning pain in the fibrous tissue, was introduced in 1976. The stiffness and fatigue associated with FMS have often been confused with rheumatoid arthritis (RA) and chronic fatigue syndrome (CFS) respectively. In fact, according to Wolfe (1993), the current definition may not be the best one because many patients who meet the criteria for CFS only differ from the FS patient in the degree of pain.
An estimated three to six million Americans may have symptoms of FMS, and make up 15 to 20% of patients seen in rheumatology practices. FMS is more common in women than in men by an approximate ratio of 20 to one. The median age of onset is from 29 to 37 years, whereas the age of formal diagnosis is 34 to 53 years, indicating that most patients endure symptoms for several years before receiving an appropriate diagnosis. Although middle-aged adults make up the majority of persons afflicted with FMS, it has also been reported to occur in children and the elderly.
Symptoms
There are several symptoms involved with FMS that involve different aspects of the body.
The five musculoskeletal or fibrous connective tissue symptoms most frequently reported are aches and pains, stiffness, swelling in soft tissue, tender points, and muscle spasm or nodules. Pain is the most prominent symptom of FMS and has been described in a variety of ways, including burning, radiating, gnawing, soreness, stiffness, stabbing and aching. Many say some degree of pain is always present and, at times, quite severe.
The widespread pain of FMS is often accompanied by significant body stiffness. Stiffness in the morning is common simply from lying still while asleep. Likewise, remaining in one position for extended periods of time, such as while driving a car, can exacerbate it. Additionally, changes in the weather can aggravate stiffness in those who suffer from FMS.
Swelling is reported in articular tissue. This is sometimes confused with joint pain as is found in rheumatoid arthritis. Tender points, frequently accompanied by muscle spasms or nodules, are critical to the diagnosis of FMS.
For those afflicted with FMS, there are symptoms relating to the nervous system, such as mood swings and depression.
Concentration and even the performance of simple mental tasks can be difficult; and paresthesia, which is a numbness or tingling sensation, can be felt in the hands, arms, feet, legs and even in the face. Many times, these symptoms suggest other problems, such as carpal tunnel syndrome and neuritis, misleading people to undergo numerous tests for such conditions, only to find that the test results are normal.
About 90% of those with FS report moderate to severe fatigue with lack of energy, decreased exercise endurance, or the kind of exhaustion associated with the flu or lack of sleep. Other related problems include migraine headaches, temporomandibular joint dysfunction syndrome (TMJ), sleep disturbance, bowel and bladder irritability, dismenorrhea, chest pains, dysequilibrium and environmental sensitivity.
Pathway of Pain
If my days were untroubled and my heart always light,
would I seek that fair land where there is no night?
If I never grew weary with the weight of my load, would I search for God's peace at the end of the road?
If I never knew sickness and never felt pain, would I search for a hand to help and sustain?
If I walked without sorrow and lived without loss, would my soul seek solace at the foot of the cross? If all I desired was mine day by day, would I kneel before God and earnestly pray?
If God sent no winter to freeze me with fear, would I yearn for the warmth of spring every year?
I ask myself these questions and the answer is plain, If my life were pleasure and I never knew pain--I'd seek God less often and need Him much less,
For God is sought more often in times of distress. And no one knows God or sees Him as plain As those who have met Him on the pathway of pain.
-author unknown
SO MANY QUESTIONS SO FEW ANSWERS
For people with chronic pain, the spinal cord becomes overloaded with input, leading it to become hypersensitive to the messages sent its way. It in turn abnormally amplifies the response so patients feel pain from contact that should have no effect.
Joseph ABCNEWS.com April 8, 2002
- Jan Murphy committed suicide last summer because she could no longer live with a disease that many doctors still don't believe exists.
She had fibromyalgia, a chronic pain condition that made a cool breeze on her skin feel like fire and caused every part of her body to ache. After CT scans and MRIs showed no medical reason for her pain, Murphy turned to Dr. Jack Kevorkian for a final solution.
"When you start hearing there is no hope, no treatment, and no cure, over and over, you lose your will to fight," Murphy wrote in a eulogy that was read at her funeral. "What most people saw of me was a shell of what was going on inside."
What exactly was going on with Murphy and other fibromyalgia patients has long been a controversial matter in the medical profession. Many doctors thought that fibromyalgia was a mental health problem, with no physical cause.
Until five years ago, grassroots fibromyalgia groups were virtually chased out of medical conferences when they tried to spread the word about the syndrome. Now, researchers at the University of Alabama have uncovered proof that what patients like Murphy experience isn't a psychological disorder, but rather is caused by abnormalities in the brain and central nervous system.
Letter to people that don't have FMS
Paula Payne and Bek Oberin
Having FMS means many things change, and a lot of them are invisible. Unlike having cancer or being hurt in an accident, most people do not understand even a little about FMS and its effects, and of those that think they know, many are actually misinformed.
In the spirit of informing those who wish to understand ...
. .. These are the things that I would like you to understand about me before you judge me...
- Please understand that being sick doesn't mean I'm not still a human being. I have to spend most of my day in considerable pain and exhaustion, and if you visit I probably don't seem like much fun to be with, but I'm still me stuck inside this body. I still worry about school and work and my family and friends, and most of the time I'd still like to hear you talk about yours too.
- Please understand the difference between "happy" and "healthy".
When you've got the flu you probably feel miserable with it, but I've been sick for years. I can't be miserable all the time, in fact I work hard at not being miserable. So if you're talking to me and I sound happy, it means I'm happy. That's all. It doesn't mean that I'm not in a lot of pain, or extremely tired, or that I'm getting better, or any of those things. Please, don't say, "Oh, you're sounding better!". I am not sounding better, I am sounding happy. If you want to comment on that, you're welcome.
- Please understand that being able to stand up for ten minutes, doesn't necessarily mean that I can stand up for twenty minutes, or an hour.
And, just because I managed to stand up for thirty minutes yesterday doesn't mean that I can do the same today. With a lot of diseases you're either paralyzed, or you can move. With this one it gets more confusing.
- Please repeat the above paragraph substituting, "sitting", "walking", "thinking", "being sociable" and so on ... it applies to everything. That's what FMS does to you.
- Please understand that FMS is variable.
It's quite possible that one day I am able to walk to the park and back, while the next day I'll have trouble getting to the kitchen. Please don't attack me when I'm ill by saying, "But you did it before!", if you want me to do something then ask if I can. In a similar vein, I may need to cancel an invitation at the last minute, if this happens please do not take it personally.
- Please understand that "getting out and doing things" does not make me feel better, and can often make me seriously worse. Telling me that I need a treadmill, or that I just need to lose (or gain) weight, get this exercise machine, join this gym, try these classes... may frustrate me to tears, and is not correct... if I was capable of doing these things, don't you know that I would? I am working with my doctor and physical therapist and am already doing the exercise and diet that I am suppose to do. Another statement that hurts is, "You just need to push yourself more, exercise harder..." Obviously FMS deals directly with muscles, and because our muscles don't repair themselves the way your muscles do, this does far more damage than good and could result in recovery time in days or weeks or months from a single activity. Also, FMS may cause secondary depression (wouldn't you get depressed if you were hurting and exhausted for years on end!?) but it is not created by depression.
- Please understand that if I say I have to sit down/lie down/take these pills now, that I do have to do it right now - it can't be put off or forgotten just because I'm out for the day (or whatever). FMS does not forgive.
- If you want to suggest a cure to me, don't. It's not because I don't appreciate the thought, and it's not because I don't want to get well. It's because I have had almost every single one of my friends suggest one at one point or another. At first I tried them all, but then I realized that I was using up so much energy trying things that I was making myself sicker, not better. If there was something that cured, or even helped, all people with FMS then we'd know about it. This is not a drug-company conspiracy, there is worldwide networking (both on and off the Internet) between people with FMS, if something worked we would KNOW.
- If after reading that, you still want to suggest a cure, then do it, but don't expect me to rush out and try it. I'll take what you said and discuss it with my doctor.
In many ways I depend on you - people who are not sick - I need you to visit me when I am too sick to go out... Sometimes I need you help me with the shopping, cooking or cleaning. I may need you to take me the the doctor, or to the physical therapist. I need you on a different level too ... you're my link to the outside world... if you don't come to visit me then I might not get to see you.
... and, as much as it's possible, I need you to understand me.
This letter was modified (with permission) and published by Paula Payne in 1996 to become the "Letter to Normals". Since then it has been printed in various publications Due to this fact, I would like to state that This "Letter to Normals" be used to help other people with FMS as long as proper credit is given to Paula Payne and to Bek Oberin (Bek wrote the Open Letter To Those Without CFIDS.) for creating it.
Fibromyalgia/Myofascial Pain Syndrome
Devin Starlanyl, M.D.
Pain is often the most prominent symptom of FMS, but there are many others, especially when MPS gets in the picture. Trigger points (TPs) cause muscle spasticity (tightness), which disrupts the flow of liquids in the body.
Your eyes may often be dry, yet at times they water.
Your thermal regulatory system is out of whack. This is noticeable when you get out of bed (often, due to bladder irritability) during the night. You then wait for your temperature to regulate after getting back in bed, before you cover up again.
Spasticity can constrict your peripheral blood vessels--those close to the skin. Then, in the winter, certain areas of your body-- most often the buttocks and thighs--feel like cold slabs of meat.
Perhaps you have "vasomotor rhinitis"--a chronic runny nose, which starts a "domino effect". It's "mechanical"--not caused by a virus or bacterium.
As you sleep, stuffiness in your nose moves from side to side as you roll.
Post-nasal drip hits the back of you throat.
Throat and neck TPs--especially in the sternocleidomastoid (SCM)-- develop satellite TPs.
You get TPs down your arm, and loss of motion in your neck and shoulders.
The constant drip into ever-more restricted vessels can result in a sinus infection, because viruses and bacteria take advantage of the situation.
Dr. Janet Travell, in her autobiography, "Office Hours Day and Night" noted that dizziness, ringing of the ears, loss of balance, and other symptoms can all be caused by SCM TPs. Dr. Travell was White House physician to John F. Kennedy. She and her partner, David Simons, wrote the definitive texts on MPS.
The tight SCM complex transmits nerve impulses that inform the brain of the position of the head and body in the surrounding space. It doesn't match the input from your eyes. When head movement changes the SCM message--when you turn, or look up from changing the kitty litter, you get dizzy.
This, coupled with poor equilibrium, can make it seem that the walls are tilting.
When we take corners while driving, we get the impression that we're "banking" the turn at a steep angle, as if we're on a motorcycle.
Cold drafts can bring on neck TPs.
Be careful how you move in bed. When you turn, roll with your head flat, and use your arms to help. Don't lift your head and "lead with it" as you roll. That puts a great strain on the neck area and "loads" TPs, just as climbing steps or walking uphill "loads" the muscles of the thighs.
A common symptom of SCM TPs is a "drunken" walk, as we bump into doorways and walls.
Muscle weakness causes much FMS grief.
This is often due to "latent" TPs.
They aren't "active"--they don't cause pain unless we press them. But if we stress them, they "give out". You try to take a drink from a glass, and end up wearing your drink. As you twist your wrist to bring the drink to your mouth, a latent TP-stressed muscle is asked to support the drink. Your body couldn't tell where the drink was in relation to your mouth, nor how heavy it was.
Learn to use two hands to carry things, not to carry heavy things, and be prepared for lots of spills.
When our muscles frustrate us, don't dwell on it. Move on. Don't berate yourself for something you can't help.
Our worst enemy isn't pain, and it isn't muscle weakness, it's negativity .
Cultivate a sense of humor. Wear printed fabrics. Use straws.
Another distressing facet of TP-inspired muscle weakness is the so- called "weak-ankle, weak-knee".
You're walking across level ground and bam! You're down. Or you "catch yourself" and avoid the fall, meanwhile stressing muscles even more.
Be cautious on steps.
Be especially careful on uneven surfaces.
Vary your tasks--use different muscle groups.
Slow your working pace.
Listen to your body.
Rest often.
Cultivate a rhythm of movement. Play music while you work, if you can.
Don't fight your body, work with it. If at all possible, lie down for a few minutes at times during the day. Muscles are constantly working to hold your head up.
Don't sit too long in any one position. When you drive, pull of the road every hour and walk around the car. Stretch.
At home, use a rocker to prevent the muscles from building up electrical activity.
When you must lift, keep the load close to your body, and look up just before you lift. That tightens the long spinal muscles and prepares your back to lift.
Added stress to the body will cause FM to flare up.
Any infection, or yeast overload, is also stress.
Disrupted carbohydrate metabolism of FM patients causes intense craving for sweets, which feed yeast. In a "Scientific American" article in the January '89 issue, the Wurtmans discuss the relationship of sleep-deprivation, melatonin, serotonin, (neurotransmitters), and carbohydrate craving.
Carbohydrate-cravers snack not because they're hungry, but because eating is used to combat tension, anxiety, or mental fatigue-- especially in the late afternoon and early evening.
The alpha-delta sleep anomaly of FM makes it just about impossible to get rest.
When morning comes, you're stiff, achy, and your muscles are unresponsive.
Your body/mind hasn't received the proper quality nor quantity of sleep it needs.
You feel as though you've had a run-in with a truck the day before, and the truck won.
Level 1 sleep (alpha stage), is the lightest sleep we get. Delta is the deepest. In delta, immune chemicals and rebuilding chemicals are created, and the body/mind is repaired.
When an FM patient enters delta stage, sleep is interrupted by alpha wave intrusion.
We never get the deep, refreshing sleep others enjoy. This is a major handicap.
Medications, such as amitriptyline, may increase the quantity of our sleep, but they do nothing for the quality.
FM patients can also get bruxism (teeth clenching and grinding), muscle spasms in the arms and legs, (myoclonus), sleep apnea and shallow breathing (check out those chest TPs).
We also feel sleepy at "inappropriate" times.
If we push ourselves "over the hump", we slide into a wakefulness/ insomnia pattern.
It's important for us to eat regularly (and not too close to bedtime), avoid stimulants, avoid alcohol, and develop regular sleep patterns.
Some of us need waterbeds, and almost all of us need cervical pillows.
Information about Medications
Devin Starlanyl, MD
This information may be freely copied and distributed only if unaltered, with complete original content.
Often, you may have to try many medications before you find the optimum ones for you. We react differently to each medication, and there is no "cookbook recipe" for FMS or MPS. What works well for one of us can be ineffective for another. A medication which puts one person to sleep may keep another awake. Each of us has our unique combination of neurotransmitter disruption and connective tissue disturbance. We need doctors who are willing to stick with us until an acceptable symptom relief level is reached. Medications which affect the central nervous system are appropriate for FMS/MPS. They target symptoms of sleep lack, muscle rigidity, pain and fatigue. Pain sensations are amplified by FMS, and so the pain of MPS pain is multiplied. FMS/MPS patients often react oddly to medications. It is the rule rather than the exception that a FMS/MPS patient will save strong pain meds from surgery or injury for when they REALLY need it -- for an FMS/MPS "flare". This is a sign that your needs aren't being met. I give you the following quotes. I hope you will pass them on to your doctor. They are from "PAIN A Clinical Manual for Nursing Practice", by McCaffrey and Beebe. Health professionals "often are unaware of their lack of knowledge about pain control." "The health team's reaction to a patient with chronic nonmalignant pain may present an impossible dilemma for the patient. If the patient expresses his depression, the health team may believe the pain is psychogenic or is largely an emotional problem. If the patient tries to hide the depression by being cheerful, the health team may not believe that pain is a significant problem." "Research shows that, unfortunately, as pain continues through the years, the patient's own internal narcotics, endorphins, decrease and the patient perceives even greater pain from the same stimuli." "The person with pain is the only authority about the existence and nature of that pain, since the sensation of pain can be felt only by the person who has it." "Having an emotional reaction to pain does not mean that pain is caused by an emotional problem. "Pain tolerance is the individual's unique response, varying between patients and varying in the same patient from one situation to another." "Respect for the patient's pain tolerance is crucial for adequate pain control." "THERE IS NOT A SHRED OF EVIDENCE ANYWHERE TO JUSTIFY USING A PLACEBO TO DIAGNOSE MALINGERING OR PSYCHOGENIC PAIN." "No evidence supports fear of addiction as a reason for withholding narcotics when they are indicated for pain relief. All studies show that regardless of doses or length of time on narcotics, the incidence of addiction is less than 1%." ] This book is so clear and so well documented that I suggested my local library buy it. I wanted everyone in the area to have access to this information. Once you read this book, you get a greater understanding of pain and pain medications, as well as coping mechanisms. Many non-pharmaceutical methods of pain control are also described thoroughly in this reference. It's normal to be depressed with chronic pain, but that doesn't mean depression is causing the pain. Maintenance with mild narcotics (Darvocet, Tylenol #3, Vicodin-Lorcet-Lortab) for nonmalignant (non-cancerous) chronic pain conditions may be a humane alternative if other reasonable attempts at pain control have failed. The main problem with raised dosages of these medications is not with the narcotic components, per se, but with the aspirin or acetaminophen that is often compounded with them. Narcotic analgesics are sometimes more easily tolerated than NSAIDs, the Non-Steroidal Anti-Inflammatory Drugs. Neither FMS nor MPS is inflammatory. NSAIDS may disrupt stage 4 sleep. Prolonged use of narcotics may result in physiological changes of tolerance or physical dependence (with- drawal), but these are not the same as psychological dependence (addiction). Under-treatment of chronic pain of MPS/FMS results in a worsening contraction which results in even more pain. "Anti- anxiety" medications are not an indication that your symptoms are "all in the head". These medications don't stop the alpha-wave intrusion into delta-level sleep, but they extend quantity of sleep, and may ease daytime symptom "flares". This is only a partial list. Stay tuned to the Fibromyalgia Network for news of more medications of possible use in FMS/MPS. Guaifenesin: Guaifenesin appears to reverse the process of FMS. It is a fairly new and experimental use. I have a whole chapter in the book on it. A flawed study was done that seemed to show it was no better than placebo. Please see the frame On Guaifenesin. Relafen (nambumetone): this is a NSAID that is often well tolerated because it is absorbed in the intestine, sparing the stomach. Benedryl:(dyphenhydramine): a helpful sleep aid/antihistamine which is safe in pregnancy. The starting dose is 50 mg 1 hr. before bed. Increase as tolerated until symptoms are controlled or 300 mgs. About 20% of patients react with excitation rather than sedation when taking Benadryl. (non-prescription) Desyrel (Trazadone): an antidepressant that helps with sleep problems. It must be taken with food. Atarax (hydroxyzine HCl): suppresses activity in some areas of Central Nervous System to produce an anti-anxiety effect. This antihistamine and anxiety-reliever may be useful when itching is a problem. Elavil(amitriptyline): a tricyclic antidepressant (TCA) is cheap and useful. It generates a deep stage four sleep. Most patients will adapt to this med after a few weeks. It can cause photosensitivity and morning grogginess. It often causes weight gain, dry mouth, as well as stopping the normal movements of the intestine. It may cause Restless Leg Syndrome. Wellbutrin (bupropion HCl): is a weak Specific Serotonin Reuptake Inhibitor (SSRI) and antidepressant that is sometimes used in FMS/MPS in place of Elavil. It can promote seizures. Ambien (zolpidem tartate): hypnotic -- sleeping pill, for short-term use for insomnia. There have been reports of serious depression. Soma (carisoprodol): acts on Central Nervous System to relax muscles, not on the muscles themselves. It works rapidly and lasts from 4 to 6 hrs. It helps detach from pain, and modulates erratic neurotransmitter traffic, damping the sensory overload of FMS. Flexeril (cyclobensaprine): this medication can sometimes stop spasms, twitches and some tightness of the muscle. It is related chemically to Elavil. It generates stage four sleep, but it may cause gastric upset and a feeling of detachment from life. Sinequan (doxepin): tricyclic antidepressant and antihistamine. It can produce marked sedation. This medication may enhance Klonopin, but can reduce muscle twitching by itself. Prozac (fluoxetine hydrochloride): anti-depressant that increases the availability of serotonin, useful for those patients who sleep excessively, have severe depression and overwhelming fatigue. Ultram (tramadol): non-narcotic, Central Nervous System medication for moderate to severe pain, in a new class of analgesics called CABAs -- Centrally Acting Binary Agents. It has a "low-abuse potential". Doctors may prescribe it more liberally than other strong pain-killers. One Internet doctor reported that 70 % FMS patients had pain control well enough that they could resume a more active life. Reports say you have to take it regularly for best benefits. Many people said it brought more alertness for longer times, and less "fibrofumble" of the fingers. It can lower the seizure threshold. Side-effects reported are grogginess, insomnia (may not be able to take at night), headache or loss of sex drive. Xanax (alprazolam): an anti-anxiety medication, that may be enhanced by ibuprofen. It must not be used in pregnancy. It enhances the formation of blood platelets, which store serotonin, and also raises the seizure threshold. When stopping this medication, you must taper it very gradually. EMLA: a prescription only topical cream, that may help cutaneous TrPs. It is a mixture of topical anesthetics. Pamelor (nortriptyline): this is used to help sleep. Some people find it stimulating, and must take it in the morning. Others use it before bed to help sleep. Some reports of depression with use. Klonopin (clonazepam): anti-anxiety medication and anticonvulsive/ antispasmodic. It is useful in dealing with muscle twitching, Restless Leg Syndrome and nighttime grinding of teeth. BuSpar (buspirone HCl): may improve memory, reduce anxiety, helps regulate body temperature, and is not as sedating as many other anti-anxiety drugs. Zoloft (sertraline): this is an SSRI and antidepressant, and is commonly used to help sleep. Tagamet, Zantac, Prilosec, Axid: often used to counter esophageal reflux. Tagamet may increase stage 4 sleep, and enhance Elavil. Paxil (paroxetine HCl): serotonin and norepinephrine reuptake inhibitor, and may reduce pain. It should not be used with other meds that also increase brain serotonin. Suggested dosage is 10 mgs (half a scored tablet) may cause insomnia or drowsiness. Effexor (venlafaxine HCl): antidepressant and serotonin and norepinephrine reuptake inhibitor. Suggested trial dosage is 25 mg, taken in the morning. Food has no affect on its absorption. When discontinuing this medication, taper off slowly. Inderal (propranolol HCl): sometimes helps in the prevention of migraine headaches, although blood pressure may drop with its use. Antacids will block its effect, and should not be used. Hismanol (astemizole): this is a potent antihistamine often given for allergies. Do not take at the same time as ketaconazole. Librax: for Irritable Bowel Syndrome. It is a combination of antispasmotic plus tranquilizer, that helps modulate bowel action. Diflucan (fluconazole): this antifungal penetrates all of the body's tissues, even the central nervous system. Very short term use can be considered if cognitive problems and/or depression is present, and yeast is suspected. Yeast may also be at the root of irritable bowel, sleep dysfunction (muramyl dipeptides from bowel bacteria induce sleep), and other common FMS problems. Potaba (aminobenzoate potassium): used to diminish fibrotic tissue. Travell and Simons recommend it for stubborn cases of myofascial pain syndrome. Do not use with sulfa. The suggested dosage 500 mg tid for 5 months. It will counteract guaifenesin. Quotane: this topical prescription ointment is helpful for TrP relief in close-to-the-surface areas not reachable by stretching. TrPs that refer burning, prickling or lightning-like jabs of pain are likely to be found in cutaneous scars. Imitrex (sumatriptan): this is available as an injectable solution or pill that will not prevent migraines, but it is effective for migraine pain in many cases. Works on serotonin release instead of blood vessel spasm, and may provide relief in less than 20 minutes. It should not be used within 24 hours of ergot (a common migraine drug) medications. It can increase blood pressure. It may cause spasm of muscles in jaw, neck, shoulders and arms. Also reported were tingling sensations, rapid heartbeat and the "shakes".
Devin Starlanyl, MD
This information may be freely copied and distributed only if unaltered, with complete original content.
DIET
This diet was recommended by Dr. Devin Starlanyl, MD in her book Fibromyalgia & Chronic Myofascial Pain Syndrome: A Survival Manual, Chapter 24.
The first guidelines Dr. Starlanyl has are to avoid the following:
refined sugar
alcohol
caffeine
foods high in saturated fats
high-calorie, high-fat, low-food-value junk food
In addition, Dr. Starlanyl and Dr. Lynne August have both found that a balanced diet of moderate carbohydrate, protein, and fat has been beneficial to people with FMS/MPS.
Dr. August has studied the intricate relationships between FMS, nutrition, and electrolytic imbalance and has successfully brought her own FMS into remission. A moderate diet containing the following ratio (based on percentages of calories, not grams):
40%carbohydrate/30%protein/30%fat for each meal and snack has enabled many people with FMS/MPS to reach their optimum weight with maximum health benefit.
It is also very important to drink lots of water! The water will help to flush toxins out of your body. Drink at LEAST 8 glasses (8oz ea.) of water every day!
Dr. Starlanyl and Dr. August recommend a book called The Zone (Sears and Lawren, 1995). There is also a sequel to this book: Mastering the Zone (Sears) that may be easier to find in bookstores. The first book, The Zone, goes into the healing aspects of this eating plan in great detail, while also giving you the basic eating plan. The second book, Mastering the Zone, includes the eating plan in great detail and has sample menus.
Dr. Sears states in his book The Zone, that this diet is of great benefit and is highly recommended to people with various diseases, including (but not limited to) MS, high blood pressure, chronic fatigue,lupus,and is also used by some olympic athletes to maximize their performance.
Dr. Starlanyl says that on this diet, people usually feel some improvement in seven to ten days. They are, however, seven to ten very uncomfortable days. She says that the headaches and fatigue can be extreme, but in one month you will see considerable improvement. In her book she states:
"This can be a tough diet, because if you really need it, you really crave carbohydrates. You try it for a few days and your body informs you "Yes, this is what you must do," because you are attacked by whopping headaches and extreme fatigue as soon as your body begins to struggle for a new balance. Your excess fat will start to break down and release large amounts of toxic substances and waste material. It is not fun. But it does work."
EXERCIZE?
I need to do some more research on this part. We all know 'what we can do', etc. This is seriously to be discussed with your DR/ caregiver. I have found the importance of massage therapy in my own battle with FMS as well as the use of products such as BIOFREEZE
Any exercize I do? Causes days of basic severe pain and/or bedrest required. Walking has been the best I can do. Not swimming, not biking, not arobics, etc. We each know what we can and cannot do.
FIBROHUGS.
This site is wonderful, with support, info and much more.
Tender Points Newsletter FREE
"BUT, I seem to hurt in different spots ALL the time..--can the pain move?....."
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