Fibromyalgia

February 9th, 2009 | by admin |

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Fibromyalgia – Causes, Symptoms and Treatment

By Peter rodrick

Fibromyalgia is an arthritis-related condition characterized widespread and the presence of tender points, or areas of the body that are particularly sensitive to pressure. Other symptoms may include disturbances, severe fatigue, , cognitive difficulties, headaches, bladder irritability and spasms, irritable bowel syndrome, jaw problems and painful menstruation.

What causes fibromyalgia?

Experts have theories about what may , but there is not enough evidence to support any single cause. Some think that people with fibromyalgia may have nerve cells that are too sensitive. Others think that chemicals in the brain () may be out of balance. Or it may be related to problems with the deep phase of sleep.

It has been suggested that sleep disturbances, which are common in fibromyalgia patients, may actually cause the condition. Another theory suggests that the may be associated with changes in skeletal muscle metabolism, possibly caused by decreased blood flow, which could cause chronic fatigue and weakness.




Others have suggested that an infectious microbe, such as a virus, triggers the illness. At this point, no such virus or microbe has been identified.

Signs And Symptoms Of Fibromyalgia.

Fibromyalgia carries many symptoms with the primary ones being pain and aching of the muscles, low energy and changes and disturbances to sleeping pattern.

Muscles can feel exhausted and can cause aching of the most of the body.

Most fibromyalgia patients have an associated sleep disorder called the alpha-EEG anomaly. This condition was uncovered in a sleep lab with the aid of a machine that recorded the brain waves of patients during sleep. Researchers found that the majority of fibromyalgia patients could fall asleep without much trouble, but their deep level (or stage 4) sleep was constantly interrupted by bursts of awake-like brain activity. Patients appeared to spend the night with one foot in sleep and the other one out of it.

Treatment of Fibromyalgia

The goal of treatment is to reduce pain, improve sleep, and relieve associated symptoms. Treatment is tailored to the individual. Some patients experience significant relief of symptoms, some find moderate improvement, and others report little or no relief. Only about 5% of fibromyalgia patients become symptom free.Most treatment regimens include medication, lifestyle changes, exercise, physical therapy, and behavior modification.

Exercise does not always help, but studies have shown that it improves symptoms in a good number of cases. If you are able, consider gradually building up to more and more exercise. Aerobic exercises which cause little ‘pounding’ such as walking, cycling and swimming are thought to be the best form of exercise to improve symptoms. Stretching exercises such as yoga may also help. A doctor or physiotherapist can advise on a suitable programme for your particular circumstances. The aim is to exercise safely and without increased pain. A typical goal to aim for is to build up exercise to 4-5 times a week for at least 20 to 30 minutes a session. However, it may take months to build up to this level.

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This is not a substitute for professional medical advice. Seek the guidance of a licensed physician if you need medical advice.

Fibromyalgia Resources

Fibromyalgia – Info From The Mayo Clinic
Fibromyalgia Symptoms

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  1. 14 Responses to “Fibromyalgia”

  2. By Carol Rooney on Apr 21, 2009 | Reply

    Is having major side effects to many medications a side effect of fibromyalgia?

  3. By Melanie on Sep 21, 2009 | Reply

    I have suffered from Fibromyalgia for about 7 years. I have had all the usual symptoms of fibro with an added symptom of my whole body swelling. I have been taking methadone, robaxin, motrin until just a few months ago. I hurt my back, which is another chronic problem, and had to return to my doctor. Not really expecting much of a change, my doctor changed my muscle relaxer and anti-inflammatory. I’m not sure if I can name the medications here, but I am going to. I am taking mobic and Zanaflex now and I have made a huge difference. The swelling is all but gone, the pain is better and I am actually able to sleep 5 or 6 hours straight, What an improvement. I hope I don’t develop a tolerance. I really dislike Fibromyalgia, my whole world was affected. I had not even heard of Zanaflex and I was a nurse for 20 years.

  4. By Clarissa on Sep 23, 2009 | Reply

    I am a 17yr survivor of Fibromyalgia and CFIDS . Four I was bed fast. I couldn’t even take care of my own needs. I had always been very active an was a manager of a local Pharmacy. Of course, I had to resign after collapsing on Aug. 11 1992. With little hope from the medical community of getting any better,as I could, I did my own research. Many years went into this process. I found supplements which helped with the energy, brain fog and immune system. I also learned of breathing techniques which helped with pain, brain fog and energy. I found with herbs, how to remove toxins from the body and the importance of riding my surroundings of chemicals. My doctor saw so many improvements to my quality of life that she suggested that I write a guide to these helpful steps. In July , I had this guide published and it is doing well locally but I want many more to be helped by what I’ve learned through much trial and error. You may check out an article in the Sep. issue of “All About Women” magazine. It is on pg 55 or 56. The online version is a bit different than the hard copy. It is on http://www.aawmag.com. I think many would find it very helpful. Thank you so much for your time.

  5. By vicki on Nov 15, 2009 | Reply

    Hey Melaine, my name is Vicki, and I have the same problem. My body swelling, and nothing is, or has helped.I have had this since (96) and low back problems. I do alot of P.T. and my back isn’t better.Will talk to my doctor about Zanaflex, and will get the Mobic, thanks for your article…………..vicki

  6. By patti williams on Dec 28, 2009 | Reply

    I was diagnosed with fibro. about 6-7 months ago after suffering with pain for about 1 year. i had back surgery about 4 years ago. about two months prior to diagnosis i got mono (EBV) and cytomegaly (CMV) virus I also had positive ANA test they ruled out lupus. I have been hospitalized two times with chest wall pain and placd on cardiac floor which they know very little about fibro. I am a RN so I know such. they actually put me through angiogram, stress testand whole nine yards of test. I told them i felf this as due to my fibro. after the third day of them just giving me dilaudid IV my MD showed up and increased my lyrica from 150mg a day to 300mg a day i am haviving probs. now with double vision and beeing very dizzy and sleepy, i still work full time as a dialysis nurse so im unable to take my lyrica until i get home, im also on cymbalta 60mg every day and xanax 2mg three times a day for panic disorder. I am allergic to NSAIDS. they did try soma which didnt help. please i need advise from some of you that have dealt with this disorder longer than i have. i am also at the point where i feel i cant continue to work full time…….please someone respond with any advise…..thank you patti

  7. By patti williams on Dec 28, 2009 | Reply

    sorry for the mis-spelling of some of my words above as I am having difficulty right now with my vision.

  8. By Judy Morrison on Feb 3, 2010 | Reply

    I have had Firbromyalgia for 29 years. I also have had chest pain and gone to hospital and had all the heart testing with no sign of heart attack. I have excercised at Curves and gone to Water Arobics. Cannot stress the body too much but walk everyday for 25-40 minutes and that helps but when starting out have lots of pain in feet and as I get halfway home the pain lessens. I am always in pain in every part of my body and can’t take Nsaids as they give me diarrhea and lots of bad gas and also pain in the kidneys. I have tried Amatriptoline 10mg and 25 but they make me so drousy and worsen my vision. I am legally blind with Macular Degeneration which I got in my late 40’s as in my case it runs in my family and I have Hereditory Macular so lost my licence to drive in l996 and I have Osteo Arthritis and two knee replacements, so I have been through the mill with Diagnosis of 18 of 18 pressure points for Fibro. I have multiple problems and lots to cry about but the way I deal with pain is mild excercise and busy my self with other things and try not to dwell on myself too much, whic is very hard to do. I rest everyday for 1 1/2 hrs anywher from 3:00 p.m. to or by 5:30 for an after dinner rest. Rest is important but you always get up feeling like you have just fallen off the back of a truck and into a ditch. Just get up and get moving and keep moving and when I can’t take the pain anymore I take 2 Tylenol extra strength and then take two more 12 hours later to break the pain pattern. You just have to think positive.

    The sleeping is a problem but sometimes I drink a couple glasses of wine or rum is fine anytime of year and takes the pain away temporarily. Not to become accustom to drinking but now and then it works. It’s good to have a partner or family member or friend that can read the symptons of Fibro and that’s important having someone who understands what you are going through for support when you need to vent a little. But you can’t moan and groan too much it drives people away from you. I guess we just have to not smoke, eat healthy and have faith that there are sometimes spells when you have relief Not everyone can be so lucky as me to have a undrstanding partner. It’s something you just have to learn to deal with, but definitely mild excercise rather than taking medication which wrecks havoc with your kidneys and causes bowel problems is part of the answer. There doesn’t seem to be a cure. It certainly messes your mind up but if you can joke about it that helps also. Just remember, laugh and the world laughs with you, cry and you cry alone. I always recall that saying when I have a pity party with myself. Good luck and keep the faith. JM pardon any spelling errors as I am visually impared.

  9. By Pat on Feb 17, 2010 | Reply

    Having suffered with this for years, I finally found a medical professional who understands it. You cannot describe it unless you have it.I am now taking along with painkillers, flexeril,mobic, have just started on lyrica. I still have bad days, but I MAKE myself stay active. Even if I have to roll out of bed. I work fulltime, and find I need to have something to get up and moving for. I am not saying that I have days I am not bedridden, because there are some. My sympathies to all. Exercise helps, even though at times I just can’t. Who wants to be the woman who complains about their aches and pains all day? I hurt right now but it is controlled. I have an active family, but some week ends I just have to REST!

  10. By julie on Feb 24, 2010 | Reply

    I have had fibromyalgia for some time now, and have started recently to have severe pain in the bottom of my feet, it feels like they are severely bruised, mostly on the heel area,it subsides when i get off my feet for a while. I also have severe back pain right in the area where my bra goes across my back , on the right side, mostly, i took lyrica for a while it helped tremendously, but my ahccs insurance wont cover it , so i am out of samples, and the withdrawal of it was terrible, hope someone finds a cure for this horrible disease, I wouldnt wish it on my worst enemy.

  11. By dolores on Apr 14, 2010 | Reply

    i read judy’s info of her’, and i can relate to what she is saying. i’ve have lupus and fibro,since 2005 when the doctors confirmed my pain. i’ve gotten off the meds that they perscribed and switched to medical marijuana. it takes away the pain alot guicker and makes me fell alot better not to mention,lots of laughter. i still have to work at dealing with the pain buti don’t have to worry about constapation.that is so difficult,hated it. oxycontin is not the answer, it puts everything to sleep and the pain is still there. i will always have pain and can have relief for a alittle while with marijuana but i won’t have to deal with the catastrophy that meds leave behind. my doctor blessed me with my decision. i don’t look like death anymore, but i do have to watch my intake of food. it makes you hungry,when before i did not want to eat because the meds kept me from going to the bathroom. i do eat healthy, i don’t eat alot of junk, but now i know i can eat and no problem having it come out. well i hope this helps someone with their pain,it’s not for everyone, i’m working at this myself cause i don’t want to use pain pills that can do more harm than good.

  12. By Jennie on May 26, 2010 | Reply

    I was diagnosed 1 year ago w/fibro, mixed connective tissue disease (lupus & schelroderma), herniated discs, osteoarthritis, bulging discs, hyatial hernia, strictions in my esophagus, hives, and signs of reynaud and God knows what else. For the last 3 months I’ve recently have had convulsions (like I’ve been shot with a tazer) on the floor convulsing and my breathing becomes labored and my primary says is all phsycological and having a terrible time trying to see a neurologist. June 1 I will have a new primary. I have medicare. Fighting to get referral after referral, due to the pain, I am now seeing a pain management dr. He has prescribed lyrica, ms contin and hydrocodone. My primary (dr moron) just kept giving me hydrocodone (10.325 7Xday) My right leg is constantly in exruciating pain. Only with the new combo in my leg feeling relief cause of pain mgmt dr. Now I can’t afford lyrica and don’t know what I’m going to do. Reading the other meds on this site helps. I stretch alot, use a rolling pin on my legs, heating pad, yoga and little walking helps. But sometimes the bottom of my feet feel so bruised and can hardly walk. I sleep approx. 4 to 5 hrs at night, now. I can deal with that instead of 3 hr nights. My insurance suggested instead of lyrica there is ethosuximide or fibronal. Left message with pain mgmt dr.. Had my whole family read about fibro and the rest for support. They are good to me. God Bless those without the support. I will pray for you. I will take any suggestions or love to hear from anyone with the same as me. Oh, found out that traditional medicare can allow you to see any specialist. It’s like a PPO (80/20) insurance. Mayo clinic will take you tomorrow with trad. medicare (no hmo’s). Open enrollment is Nov 1st unless, financially troubled, you can switch immediately with a visit to social security office and apply. God Bless you all. I know the pain and how it turns you life upside down. Don’t give up and don’t be afraid to try new medication. Jennie

  13. By robin on Jun 14, 2010 | Reply

    I have been dealing w/fibro for yrs. but my PCP is one of those flipping idiots that did not beleive fibro. exisited he kepted saying I just pulled a muscle! WHAT!? has he lost his damn mind? I guess I pulled a muscle in my ass,back,hips,shoulder,legs,arms, ect…… I finally got mad and told him to piss off! and I took it matters in my own hands I started doing research you have got to be your own advocate because believe me no one else knows you but you! and here is my conclusion so far lyrica only works for people not allergic to or cannot tolerate NSAIDS and if you are not careful you will gain alot of weight,it also can cause you to feel like you are completely losing your mind! and dear God I sweat in a cold shower, my hands & feet felt like they were going to exploded the swelling was unbearable! I go for days w/out sleep and sometimes I would do nothing but sleep?! finally after being on 450mg a day for almost a year I told the Dr. NO MORE NO WAY!Iam now of that and feeling better I started taking neurontin(Gabapentin) it is a nerve blocker,mobic,wellbutrin XL 24hr.,trazodone(sleep aide),soma(carisoprodol-muscle relaxer,skelaxin(metaxalone-muscle relaxer)and of coarse lomotil for IBS w/diarrea THANK GOD Iam on of the luckier ones that do not have constipation! Iam sorry for the ones that do! I do have other problems other than fibro I also contend with osteoarthritis,digenitive disk disease,carpol tunnel,bursitis,& major feet problems,hyatial hernia,ect…….. for anyone whos insurance won’t cover your meds.appeal it!the feet problem is called plantar facsitis(muscle in the heel of foot)NEED TO SEE ORTHOPEDIC FOOT DOC.it feels like knives in bottom of feet! PLEASEEEEEE try to stay away from narcotics they will ruin your liver&kidneys lyrica,mobic,and almost any drug that treats fibro.will do that to so have blood tests done at least every 3 or 4 months! to make sure that does not happen to you! also, cymbalta & the other anti-depressants that they give for fibro. is VERY dangerous please watch dosage & side effects! you do not want to O.D.or become suicidal! pain management doc. are great! get one! aquatic theropy is FABULOUS! BY THE WAY,I have TOS thorastic outlet syndrome it only occurs in about 4% of the population & I guess the jokes on me! they want to remove my number 1 rib(it is up in the neck region)& remove the muscles & nerves that surround it from the no.1 rib to the no.4 rib which happens to all be around all the main arteries from your neck area to your heart. and since I have fibro. they feel that it is going to be im-operable unless I start to lose full mobility in my left arm & of coarse Iam left handed so Iam going to see a cardiovascular surgeon & a nerologist so hopefully they can come up with a plan to solve this delema that Iam in. Well,good luck to all & I hope I was helpful if anyone has questions or concerns I have a vast wealth of knowledge on alot of different health concerns I have a mom who has been a trama nurse for 43yrs.& her husband is a doctor currently serving in Iraq. MAY GOD BLESS EVERYONE AND KEEP YOU WELL!! AND GOD BLESS AMERICA!!!!!!! ROBIN

  14. By becky burns on Jul 18, 2010 | Reply

    dear robin, my name is becky and i have everything that you have except the tos.my dr. diagnosed me with fibro.about 5yrs.ago andi,ve been on everything you have been on.just last month my dr. upped my dosage of lyrica to 600mgs.a day but i have gained 60lbs. in just 2yrs.,along with my feet swelling.it hurts when i walk sit or stand .i have had 2heel surgeries, one in 08 09 3 knee surgeris the last one being on feb.4th. of 2010.i,m only 5ft1 and now he hhas taken me off my soma,skelaxin and getting him to give me anything differant for pain is like pulling teeth out of a mule.go figure i have seen this dr. for 11yrs. in jan.do you have any thought in this matter that might help me.i,m at my witts end i also have suffered bypollar manic depressive for yrs.i don,t take half the meds. for that because it seems eveything makes me gain weight please help.B.B. in Texas

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