National Display of Information on FM
Awareness is wonderful and I am grateful for this, but I am dismayed that a network program, "The Doctors" would not do a better job researching their program topic. As you will see if you click on the link provided, they call the "tender points" of FM "trigger points." Trigger points are myofascial areas of knotted up muscle fibers in a taut band of muscle. They are EASILY felt unless behind bone or other muscles, or the band of muscle affected is too tight, in which case myofascial massage is necessary to loosen the muscle to locate the (TrP).
Myofascial TrPs are palpable, rendering an objective measurement of disease. When these TrPs are treated with pressure therapy, injections, or dry needling, the "twitch response" is visualized by the practitioner and felt by the patient. This has not been described in the "tender point model" of FM, or the diagnostic criteria set by the American College of Rheumatology (ACR).
Let me interject that a newer study by Hy, Wang and others, "The Predetermined Sites of Examination for Tender Points in Fibromyalgia Syndrome Are Frequently Associated With Myofascial Trigger Points. J Pain. 2009 Nov 13. [Epub ahead of print]" suggests that possibly all FM patients also have CMP (chronic myofascial pain from trigger points). If and when this study is replicated, it brings question, "Were the ACR patients screened for the presence of myofascial trigger points?" "Did the examiners know enough about TrPs to know to look for them or that cause significant pain, dysfunction and referral of symptoms?" "Did they know presence of these TrPs provides criterion that takes FM out of the subjective complaints only arena?" When the study is replicated, it will bring about many questions that I personally would like to see answered. What we know for certain right now is that FM, and CMP, can and often do co-exist in the same patient, yet paradoxically not all patients with myofascial trigger points have FM, they are two separate entities.
As I have described before, and backed by solid research, FM is a central sensitization problem brought on by a dysfunction of the HPA (hypothalamus-pituitary-adrenal) axis. Chronic myofascial trigger points and pain (CMP) is a peripheral nerve to muscle problem. (Hong, et al). FM, CFID, migraine, IBS, irritable bladder and several other common co-existing conditions that escape me right now, also have a strong central nervous system component. As an example the pain of a cervicogenic migraine, is helped a great deal by myofasical therapy. When any of these disorders co-exist with CMP, the peripheral message of painful trigger points to the brain keeps the brain in a hypersensitive state," causing a "wind up" phenomenon and dysfunction of the HPA-axis (also seen in CFID/CFS/ME) is off and running. Think about the patient that has FM, CFID, CMP, migraine, IBS, and irritable bladder. You may be one, I am.
In disturbs me that so much misinformation is being disseminated, well intended, but could lead to a misdiagnosis and inappropriate treatment. It is this misinformation that causes unnecessary frustration to both the doctor and the patient.


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Hello....I would like to encourage anyone who has chronic pain to ask your doctor to check your Vitamin D level....which is so very important...this is a simple blood test....but the test is not a common thing that doctors do....there has been a lot of recent research on Vitamin D and just how important it is to everyone...I have had FM since 2005 and I have learned how to "control my FM pain" by taking vitamins and supplements...my D level was around 12 when I went to talk to a surgeon about a parathyroid problem that I had. The surgeon thought that all of my pain was from low Vitamin D...(I did have a parathyroid problem though) but part of my pain was due to low Vitamin D...
I now take a magnesium and malate combination supplement (found at vitamin store) Omegas, Vitamin D supplement, Calcium and Super B Complex...plus others...but these are the ones which help my FM pain the most...
FM is a very painful illness and one that a lot of doctors do not understand...
and it takes a trial and error process to figure out just what the body needs to cope better with it...it took me a long time to figure out what I needed....and it takes at least 6-8 weeks for you to "feel a difference"....there are no quick fixes to this dreadful illness...
I would encourage everyone who has FM to get the Vitamin D level tested...
Odds are this is part of the pain that you have....
Absolutely. Low vitamin D has also been linked to cancer. Mine was low normal. I had a weird experience though, nothing new for an FMer is it? I got a metalic taste in my mouth. I have now dropped back to 1/2 D3 every other night with my calcium, and slo mag (I have osteopenia, and constipative alternating water loss irritable bladder syndrome and calcium add to that, and straight mag. causes severe abdominal cramping. I also have delayed gastric emptying). Great on the mag. We don't know yet exactly what magnesium does, but we are finding out more and more. I can't say that any of this has helped with MY pain, but we are all different, with different co-existing conditions. The most important part, I think, is that we pay attention to what our body is telling us. Track changes, and see if a pattern of pain and fatigue emerge or abate with that new supplement, medication, or treatment.
Lamb hugs and thanks for sharing this most important information.