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Fibromyalgia was recognized by the American Medical Associatio­n as an illness and cause of disability in 1987. In the early 1900's fibromyalgia was considered "arthritis of the muscles" and classified with other rheumatological conditions involving pain in the muscles or joints.

Stress and pain are irreversibly linked in fibromyalgia. For many people, some kind of stressful event is what initially triggers the illness. It often shows up after a serious illness, some kind of emotional or mental shock or with PTSD (Post Traumatic Stress Disorder).

Today fibromyalgia is thought to be a central nervous system disorder in which either pain sensing nerves are sensitive, or the brain is extremely sensitive to pain impulses. People with fibromyalgia are out of balance in the HPA axis -hypothalamus-pituitary-adrenal-which is our body's system for responding to stress with neurochemicals like adrenalin and serotonin. Though fibromyalgia feels different to each person, the common denominators are painful and uncomfortable sensations throughout the body, fatigue and mental cloudiness.

Adding insult to injury is the fact that you may still appear healthy to everyone else, no matter how badly you feel, so that few people understand how compounding these conditions can be on a daily basis.

Stress reduction in an important part of managing fibromyalgia. Here are a few ways that may help you alleviate some of the stress. 

  1. Good self care. Eating a nutritious diet, getting the right amount of the right kind of exercise, establishing regular sleep habits and giving yourself grace are all part of taking good care of yourself.
  2. Change the way you think. This takes practice, yet it gives you a chance to respond to situations instead of reacting.
  3. Practice body awareness. People who deal with chronic pain, as in fibromyalgia, become accustomed to ignoring their bodies; it's one way they cope with the pain. If you learn to recognize your body's cues that you are becoming tense, you can use a relaxation technique or exercise early on, before stress becomes unmanageable.
  4. Keep stress journal. This has two purposes. You can journal about stressful incidents and use the journal as a tool to help you identify situations that are stressful to you. This can help you either avoid repeating these situations or be better prepared should they be unavoidable. Journaling about a stressful event also helps you debrief and de-stress after the event.
  5. Learn stress management techniques, such as visualization, meditation, and breathing. These techniques decrease the level of neurochemicals circulating in your body, and help decrease both stress and pain.
  6. Chiropractic adjustments may help reduce pain and improve range of motion. Chiropractors use a wide variety of manipulative techniques and can individualize your treatment.
  7. When you decrease your stress, you will probably experience less pain and fatigue from fibromyalgia. Changing your lifestyle so that you are taking care of your self can help prevent flare-ups and give you a better quality of life. Eat well, think well, and move well.
  8. NeuroEmotional Technique (NET) focuses on releasing emotional blocks stored in the body's memory through simple chiropractic adjustments. Everyone has emotional trauma, past or present.

    D-Ribose in Fibromyalgia and Neuromuscular Disease


    Fibromyalgia is a common, nonarticular, rheumatic syndrome that affects the upper and lower body, right and left sides. Concrete diagnosis of fibromyalgia is difficult since many other diseases and conditions present with similar symptoms and there are no laboratory tests that can be used as a primary diagnosis. As a result, accurate diagnosis must be made by excluding these other diseases or conditions. The American College of Rheumatology has defined the clinical diagnosis of fibromyalgia following two criteria: 1) widespread musculoskeletal pain in all four quadrants of the body for at least three months, and 2) tenderness at 11 or more of 18 specific tender points (or trigger points) located on the upper back and chest, insides of the elbows, lower back, upper thighs and front of knees.

    Patients suffering with fibromyalgia suffer from constant pain, sleep disturbances, overwhelming fatigue, weakness, muscle stiffness and soreness, headaches, irritable bowel, anxiety and depression. The condition is most commonly diagnosed in females, aged 20 to 50 years, and is generally treated by analgesic drugs and antidepressants.

    While a great deal of popular press can be found discussing the disease, scientific research is, in large part, lacking. However, many conclusions can be drawn from the scientific press.

    Fibromyalgia, Stress and the Brain Body Connection

    The cause of fibromyalgia is unknown, but it has been associated with stress, tension, trauma, overexertion, hormone deficiency diseases (particularly thyroid disease), alterations in brain chemistry, anemia, parasites, and viral infections. Conditions that may be associated with, or mimic, fibromyalgia include chronic fatigue syndrome, myofacial pain syndrome, carpal tunnel syndrome, mitral valve prolapse, Raynaud's syndrome and rheumatic disease.

    Energy Status of Fibromyalgic MusclePathophysiology of Fibromyalgia

    Examination of the vastus lateralis muscle of the quadriceps group, trapezius and brachioradial muscle has shown that the blood flow to the tissue is lower in fibromyalgia patients than normal controls leading to low tissue oxygenation levels. 2, 4, 8-10 Electron microscopic evaluation of the capillaries supplying the trapezius showed thickening and derangement of the capillary wall. 2 Further, examination of small muscle fibers revealed mitochondrial derangement in fibromyalgia patients. 2, 4 These small muscle fibers were not found in normal subjects. Reduced blood flow, changes in capillary wall thickness and structural changes to the mitochondria contribute to hypoxia, decreased oxidative phosphorylation, lower ATP synthesis and reduced levels of adenine nucleotides in fibromyalgic muscle. Since it is postulated that the pain associated with fibromyalgia is of nociceptor origin 4, the primary hypothesis is that any condition that could lead to constant muscle hypoxia, and prolonged energy deficiency, might be a cause of fibromyalgic pain.

    Patients with fibromyalgia generally demonstrate reduced exercise capacity, with muscles that lack contractile force and endurance.10,11,13 Since these conditions are frequently associated with abnormal metabolism, many studies have investigated muscle metabolism in fibromyalgia using both traditional biopsy techniques12 and nuclear magnetic resonance spectroscopy (P-31 MRS).10,13-18 Muscle biopsy studies investigating the metabolism of ATP, creatine phosphate (PCr), ADP, AMP, pyruvate and glycogen have shown that levels of PCr and ATP are significantly lower (21% and 17%, respectively) in fibromyalgic muscle and the synthesis of PCr, the most important store of high energy phosphate in the cell, is defective. Biochemical studies have confirmed that energy metabolism is abnormal in fibromyalgia, requiring appropriate metabolic therapy.

    P-31 MRS studies are even more revealing. P-31 MRS looks directly into the muscle to determine the absolute values of energy compounds, muscle pH and changes in metabolism as they occur at rest and during exercise. Magnetic resonance spectra of the quadriceps muscle have shown that resting levels of ATP are 15% lower in fibromyalgia patients than in normal controls and during exercise PCr and ATP levels are also significantly lower (each 15%). In addition, during exercise there is an increase in metabolic breakdown products of ATP (phosphodiesters), indicating abnormal ATP metabolism and disruption of cell membranes, both associated with muscle disease.

    The energy reserve, or phosphorylation potential (PP), and the ability to utilize oxygen (total oxidative capacity or Vmax) have been determined using P-31 MRS.

    The poor bioenergetic status of muscles in fibromyalgia may be due to reduced blood flow to affected tissue and thickening of capillary walls, leading directly to reduced levels of ATP, lower energy reserves and oxidative capacity (Vmax) and abnormal levels of phosphodiesters. The additional complication of impaired oxidative phosphorylation in the mitochondria and diminished glucose metabolism, both lowering ATP turnover, suggests that fibromyalgic muscle is energy starved. Decreased levels of ATP and changes in energy metabolism have also been found in the red blood cells of fibromyalgia patients19, suggesting that fibromyalgia may be a more systemic problem than originally thought, possibly impinging on other organ systems.

    The metabolic abnormalities in fibromyalgic muscle have been well established and show multiple interactions that may impact on the clinical symptoms. Decreased numbers of capillaries that reduce oxidative capacity may increase pain, while thickened capillary walls lowering oxygen delivery and abnormal mitochondria lead to fatigue and weakness. All are associated with reduced levels of ATP and energy metabolism that, in turn, leads to disruptions in calcium stasis, muscle soreness and stiffness. At the same time, these metabolic changes are coupled with morphological changes in the muscle that continue to exacerbate the problem with metabolism.

    Mean PP is significantly lower in fibromyalgia patients and Vmax is also significantly reduced. These findings are consistent with reduced oxidative phosphorylation and ATP synthesis in the muscles of fibromyalgia patients and may translate into the clinical symptom of fatigue.

    Ribose in Maintaining Tissue Energy Stasis

    Tissue hypoxia leads to a progressive depression of the cellular purine nucleotide pool creating an energy deficit. The adenine nucleotide ATP is the primary energy source of all living cells. In tissues subjected to the metabolic stress of hypoxia or ischemia, ATP is broken down and the metabolic machinery to recycle expended energy is disrupted. As such, adenosine diphosphate (ADP) levels accumulate leading to a series of reactions undertaken by the cell to balance ATP/ADP ratios and maintain energy stasis. These reactions ultimately lead to increased concentrations of adenosine monophosphate (AMP) in the cell. In a further effort to control energy balance, heart and muscle cells catabolize AMP, in reactions catalyzed by 5'-nucleotidase and AMP deaminase, respectively, to form inosine, hypoxanthine and adenine. These catabolic end products are washed out of the cell netting a reduction in the total pool of adenine nucleotides available to the tissue and lowering its phosphorylation potential (Figure 2). Up to 90% of these catabolites can be biochemically salvaged and recycled.

    The availability of phosphoribosyl-5-pyrophosphate (PRPP) is rate limiting in adenine nucleotide synthesis and salvage pathways required to restore nucleotide pools and rebuild cellular energy stores.20-23 PRPP is formed through a pyrophosphorylation reaction from ribose-5-phosphate that is, in turn, synthesized from glucose via the Pentose Phosphate Pathway (PPP; or Hexose Monophosphate Shunt). The activity of the PPP varies between organs, with those synthesizing fatty acids and sterols being most active. The rate limiting enzymes in the PPP, glucose-6-phosphate dehydrogenase.

    The rate of recovery of depressed energy levels following ischemia and/or hypoxia is important for functional recovery of ­muscle20,21,23,24, providing adequate levels of AMP and ADP necessary for complete repletion of ATP. Blocking the degradation of adenine nucleotides, or by providing metabolic supplementation to enhance nucleotide recovery via the salvage or de novo pathways are potential solutions to maintaining energy stasis.


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    3. Guymer EK, KJ Clauw. Treatment of fatigue in fibromyalgia. Rheum Dis Clin North Am 2002;28(2):67-78.

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    9. Lund N, A Bengtsson, P Thorborg. Muscle tissue oxygen in primary fibromyalgia. Scan J Rheumatol 1986;15(2):165-173.

    10. Strobl ES, M Krapf, M Suckfull, W Bruckle, W Fleckenstein, W Muller. Tissue oxygen measurement and 31P magnetic resonance spectroscopy in patients with muscle tension and fibromyalgia. Rheumatol Int 1997;16(5):175-180.

    11. Schachter CL, AJ Busch, PM Peloso, MS Shepard. Effects of short versus long bouts of aerobic exercise in sedentary women with fibromyalgia: a randomized controlled trial. Phys Ther 2003;83(4):340-358.

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    13. Lund E, SA Kendall, B Janerot-Sjoberg, A Bengtsson. Muscle metabolism in fibromyalgia studied by P-31 magnetic resonance spectroscopy during aerobic and anaerobic exercise. Scan J Rheumatol 2003;32(3):138-145.

    14. Krapf MW, S Muller, P Mennet, T Stratz, W Samborski, W Muller. Recording muscle spasms in the erector spinae using in vivo 31P magnetic resonance spectroscopy in patients with chronic lumbalgia and generalized tendomyopathies. Z Rheumatol 1992;51(5):229-237.

    15. Park JH, P Phothimat, CT Oates, M Hernanz-Schulman, NJ Olson. Use of P-31 magnetic resonance spectroscopy to detect metabolic abnormalities in muscles of patients with fibromyalgia. Arth Rheumatol 1998;41(3):406-413.

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    17. Kushmerick MJ. Muscle energy metabolism, nuclear magnetic resonance spectroscopy and their potential in the study of fibromyalgia. J Rheumatol Supp 1989;19:40-46.

    18. Sprott H, R Rzanny, JR Reichenbach, WA Kaiser, G Hein, G Stein. 31P magnetic resonance spectroscopy in fibromyalgic muscle. Rheumatol (Oxford) 2000;39(10):1121-1125.

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    21. Brault JJ, Terjung RL. Purine salvage to adenine nucleotides in different skeletal muscle fiber types. J Appl Physiol. 2001; 91: 231-238.

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    23. Williamson DL, PM Gallagher, MP Goddard, SW Trappe. Effects of ribose supplementation on adenine nucleotide concentration in skeletal muscle following high-intensity exercise. Med Sci Sport Exc. 2001; 33(5 suppl).

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    28. Wagner DR, Gresser U, Zollner N. Effects of oral ribose on muscle metabolism during bicycle ergometer in AMPD-deficient patients. Ann Nutr Metab. 1991; 35: 297-302.

    29. Gross M, S Reiter, N Zollner. Metabolism of D-ribose administered to healthy persons and to patients with myoadenylate deaminase deficiency. Klin Wochenschr. 1989; 67: 1205-1213.

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    31. Patton BM. Beneficial effect of D-ribose in patients with myoadenylate deaminase deficiency. Lancet. May 1982; 1701.

    32. Salerno C, D'Eufermia P, Finocchiaro R, Celli M, Spalice A, Crifo C, Giardini O. Effect of D-ribose on purine synthesis and neurological symptoms in a patient with adenylsuccinase deficiency. Biochim Biophys Acta. 1999; 1453: 135-140.

    33. Salerno C, M Celli, R Finocchiaro, P D'Eufemia, P Iannetti, C Crifo, O Giardini. Effect of D-ribose administration to a patient with inherited defect of adenylosuccinase. Purine Metabolism in Man IX. Plenum Press, New York, 1998.

    34. Gebhart B, JA Jorgenson. Benefit of ribose in a patient with fibromyalgia. Pharmacother 2004;24(11):1146-1648.

    Ribose has been extensively studied in both hearts and muscles. Safety data is well accepted, with no noted significant adverse reactions. Experiments on the use of ribose to enhance myocardial and skeletal muscle adenine nucleotide synthesis and salvage have involved both animal and human investigations and the effects of ribose in hearts are not species specific.26 Exogenous ribose administration provides the metabolic support required to bypass the rate limiting enzymes of the PPP, form PRPP and restore energy stasis in metabolically stressed muscle.

    The effect of ribose treatment in myoadenylate deaminase deficiency (AMP deaminase deficiency) and adenylosuccinase deficiency has been well documented. Like fibromyalgia, these conditions lead to progressive depletion of cellular energy pools, leading to muscle pain, soreness and stiffness. The beneficial role in energy recovery in these disease conditions with ribose treatment is suggestive of its role in energy recovery. As in the case of myoadenylate deaminase deficiency, reports from fibromyalgia patients34 indicate a reduction in fatigue, muscle soreness and stiffness associated with the condition. While further research continues, it appears that ribose can play a beneficial adjunctive role in metabolic treatment of fibromyalgia.

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