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Symptoms > Fatigue > How To Beat Fatigue
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How To Beat Fatigue

Fatigue is a mysterious and persistent foe, but you can beat fatigue and feel more energetic than ever

Everyone gets tired. That is how the body signals it needs to rest and recharge. Overwork yourself physically and you feel it in your muscles or joints. Overwork yourself mentally and you need a break. But when your need for rest seems excessive or becomes disruptive – thwarting your productivity, making everyday tasks seem daunting, robbing you of enjoyment and interaction with others – what once may have been tiredness has become fatigue. But rest assured: There are viable fatigue treatments and means to beat fatigue.

Fatigue often means something sinister is lurking. The symptom accounts for 10 million doctor office visits each year, many of who are by people with arthritis-related conditions. Up to 98 percent of people with rheumatoid arthritis (RA) report fatigue, as do 50 percent or more of those with lupus or Sjögren’s syndrome. The percentage grows higher when obesity, depression, fibromyalgia, congestive heart failure, lung problems or chronic headaches are present, too.

Because so many people with so many different medical problems experience fatigue, doctors have a tough time sorting out causes. Here we take a look at what could be behind your zapped energy and help you learn how to beat fatigue.

The challenge of fatigue

Fatigue is hard to describe and harder to diagnose. If you find yourself with no energy even after a full night’s rest, it may be fatigue. But understanding fatigue requires more than understanding the body’s normal need for rest.

Martha Grant, 53, of Berkeley, California, knows fatigue all too well. Except for a brief respite in her early 20s, she’s struggled with it since her diagnosis with juvenile rheumatoid arthritis (JRA) at age 11. “Most people feel well as the norm and then get the flu for a few days. For me, living with fatigue is like having the flu every single day,” she says.

In a study of how people with RA perceive fatigue, Sarah Hewlett, PhD, senior lecturer in Rheumatology Health Professions at the University of Bristol in England, found patients described fatigue as “severe weariness and dramatic and overwhelming exhaustion attributed to inflammation, working the joints harder and getting unrefreshing sleep.” Patients with various chronic diseases experience fatigue as an occasional come-and-go symptom, but many RA patients experience long-lasting fatigue, says Ken Pischel, MD, head of the rheumatology division at Scripps Clinic in La Jolla, California. Their bouts of fatigue sometimes seem unwarranted because they usually aren’t preceded by excess activity and may even occur when their joints are feeling good.

As such, patients have a hard time telling their doctors what may have led to the fatigue. In Hewlett’s study, the few RA patients who felt comfortable discussing fatigue with their doctors still reported inadequate care for it, perhaps because of the emphasis on more measurable physical problems, or perhaps because pain is usually eased with medication, whereas a fatigue treatment isn’t that straightforward. In often-rushed appointments, doctors may only be able to confirm fatigue’s existence, but Hewlett says this offers little help to patients.

Grant agrees. She knows the “Oh dear, here we go again” look from doctors when she brings up her fatigue. “Doctors don’t want to hear how tired patients feel – I think it makes them feel uncomfortable because they can’t fix it,” she says.

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Jim
02 Mar 2010, 14:45
Ok, so the minority (men) need to speak also. I have RA and have real issues with fatigue. It feels like I am walking through deep mud at times. Like some of you I have found that concentrating on other things does help. Here is my own tip: To battle fatigue on my job I listen to music! I have a technical job and am somehow able to focus on the music and my work as well. Try that one on for size.
Elaine
17 Feb 2010, 11:20
Oh how I understand the above comments.

I have the type of mind frame that I won't let illness defeat me but after a year of very little sleep, (I could fall asleep but it only lasted two hours) and pain all over my body that was so bad I didn't know how I was going to keep working. I went to the doctors. Two years later with visits to many doctors and every conceivable test coming back "OK" I thought I was going crazy. Then a neurologist asked me if I had seen a rheumatologist, "no" said I thinking here's another doctor to tell me that there is nothing wrong! Fortunately this wonderful doctor set my mind at ease (I wasn't going mad after all)and diagnosed Fibro. It's not a disease but a syndrome I was told. Here I am over twenty years later still in the holds of this "syndrome", with additional problems due to the many pills I have taken, gastric, intestinal etc. and not to say the least memory and attitude problems. I get so upset with some of the "nasty" side effects of the "intestinal" problems that I get off all of my meds to clear my system and live more normally (not having to ask "Where's the nearest toilet!"). I must admit that regardless of what I have taken none of the meds have really taken away the full pain. Of the ones that seem to be good the main side effects are a greater tiredness and loss of sharpness of memory (not good when you have to work! AND WEIGHT GAIN.

I am now retired so I can give in to the lack of sleep, pain etc. BUT I truly feel by giving into FIBRO (like any other illness) we defeat ourselves. In the beginning I was very much into fitness, I gave it up because I couldn't stand the PAIN but looking back I feel I should have continued with arobics to keep my tendons and muscles more limber. So my advise to all of us Fibro's is to exercise gently to keep ourselves limber.

I have found with myself that I must do everything possible to NOT GET a cold or the flu. These are murder on my system.

My top dislike when we go to the doctors with another health issue is "when they know we have "Fibro", the first thing out of their mouths is "oh well this is most probable related to your "Fibro"! I wish we could train the doctors not to think this, because we can get ill without any relation to "Fibro"

Good Luck with your ILLNESS!
Sherri
05 Jan 2010, 13:35
I am permanently disabled with OA, Fibromyalgia, Spinal Stenosis and Ulcerative Colitis. I am now taking Savella for the Fibro. It has been a life saver for me. Just to get control of some of the pain. It was difficult to get approved through the insurance company. But it was worth it. I also take Remicade treatments for the spine and Ulcerative Colitis and a polefera of other medications. But the Savella has made the biggest difference in my quality of life in the my treatment for the past 20 years.
SANDRA
16 Nov 2009, 22:12
I WAS A NURSE FOR MANY YEARS UNTIL THE FIBROMYALGIA AND FATIGUE GOT SO BAD THAT I COULD NOT DO MY JOB ANYMORE. I WAS DIAGNOSED WITH FIBRO IN 1998 AND WORKED UNTIL 2002. NOW I CAN BARELY ATTEND ONE FUNCTION OR GO TO ONE STORE WITHOUT BEING COMPLETELY EXHAUSTED. I DO MY MORNING CARE IN STAGES.THE ONLY THING THAT REALLY HELPS ME IS TO LIE DOWN AND APPLY HEAT TO THE ACHING AREAS, SOMETIMES MORE THAN ONE AREA. MOST PEOPLE DO NOT UNDERSTAND THE PAIN AND FATIGUE. IT MAKES YOU FEEL 100 YEARS OLD.
Jodi
05 Nov 2009, 12:13
Katerina,

I'm a nurse also, I know exactly what you mean. I work in an office and there are times by the end of the day my husband has to come and help me get out of the car because I can't get out and into the house by myself. Then I sit in a chair watching him fix supper and clean up, do laundry, housework, ect because I can't do it anymore. It's all I can do to work the 40 hour a week job I have. I try so hard to stay positive and get out of bed every morning and get to the job but I know that at some point, I'm not going to be able to work anymore and then we will lose out medical insurance. ( My husband is disabled) If they would just recognize the disease and work with you to help your individual symptoms and needs it would help so much. I am so fortunate that my PCP does understand and does all she can to keep me on my feet but I know many others aren't so lucky in their choice of doctors. Many still don't acknowledge that Fibromyalgia is a disease. I don't know who is finally going to listen in the medical world but please know that those who read this know how you feel and are pulling for you. I don't know your options, if there is a pain management specialist in your area or if another PCP might listen and treat you but don't give up. Go to every doctor you can until you find someone who will help. You can be helped to stay on your feet as long as you can, with medications and the right exercise program. I had a hard time finding a water therapy place but it helped me so much when I did find one and go. I know these measures won't last forever but as long as they work, I'll keep working. After that, who knows? Maybe by then it will be recognized and treated differently than it is now. Hang in there!
Katarina
04 Nov 2009, 18:37
After being ignored for years about my compalints of extreme body pain and debilitating fatigue by my PCP,I was finally listened to by a doctor at a walk in clinic. He ordered labs that showed an elevated ANA, SED rate and many others that were abnormal, which indicates an autoimmune disease. The labs were sent to my new PCP who referred me to a small town rheumatologist who diagnosed Lupus and put me on Prednisone and Plaquinil and kept telling me to wait and see how it goes. Frustrated with being ignored again,I made an appointment with a rheumatologist at a city teaching hospital who diagnosed fibromyalgia and immediately took me off the Plaquinil and weaned me off the Prednisone and told me he only treats Lupus, referring me back to my PCP who doesn't want to treat the fibromyalgia. I then went to a big city specialist who told me "FIBROMYALGIA IS NOT A DISABILITY"!!!! How can this woman treat people in crisis with no empathy or understanding of the disease! I wonder when was the last time she had debilitating fatigue and couldn't get out of bed!
I am now at risk of losing my job as a nurse because I cannot keep up the physical pace of my job.
Why doesn't the medical world think fibromyalgia is debilitating, devastating, life changing, heart breaking,unbearable, incapacitating and overwhelming,
causing anxiety, depression, chest pain, brain fog, blurred vision........excessive medical bills.....who is going to listen???
Jodi
04 Nov 2009, 09:34
I have RA, OA and fibromyalgia and know how those of us with this horrible, draining fatigue and pain that stays at a 7-8 on the pain scale on a good day feel. Some days just getting out of bed is a challenge but I have found that the days I give in and say " OK, I'm staying in bed and not moving because I'm so tired and I hurt so badly" are worse days than when I make myself get up and get moving. It's no fun and I hate it but I have to keep trying because the alternative is to end it ( not an option, really. I don't want to have to explain to God why I took over His job!), or lay in bed and hurt so badly I can't stand it. I'm on Lyrica, sulfasalazine, methotrexate and two pain meds that help some.These diseases don't give us a good option. Please, everyone hang in there and do the best you can to live your life as best you can and with as much joy you can. It's so hard but it can be done. The ones who love you will be glad you did.
Lorena
03 Nov 2009, 18:14
Is it possible that the trimestral use of remicade,can help a bipolar to reduce the intensity of the mania, and stabilised this person, letting him having a normal life. He didnt know he suffers this bipolar disorder, and now he seems to be very normal, since he is having this remicade injection trimestrally?
ali
19 Jul 2009, 19:00
I seem to have my pain under control, but the fatigue has been a problem with all aspects of my life. Last year I got married and ths year I lost my father. The stress of both events has sent some of my symptons into overdrive. I shoule be a happly married newlywed and I am always tired. I feel really bad for my husband.
Jill
29 May 2009, 23:30
I got RA 22 yrs ago with a lot of pain. Then I got an eye desease and wanted to die. My eye doctor told me no cure and to seek help. I didn't know where to go. Today I am a lead Coordinator for the visually impaired and blind. I have been with them for 12 yrs now. It was hard helping them and wearing splints on both hands, sometimes I didn't think I could get dressed. To sum it up I am like brand new because of helping people and getting my mind off myself. My members always thank me but they are the ones that help me feel better with my RA and of course with my eye desease. Just remember helping others will help you.
ghada
25 May 2009, 09:47
I HAVE FIBRO AND OVERALL FATIGUE 18+YEARS .NO ONE FEELS MY PAIN .I'D RATHER SHOOT MYSELF TO STOP THIS VICIOUS CIRCLE.I AM ON LYRICA AND HYDROQUINE.NEED ADVICE TO REMOVE PAIN ONCE AND FOR ALL.
Audrey Atherton
25 May 2009, 08:17
I have had fibro for about 12 years. Nothing helps. I have tried Tylenol 4 and am on Lyrika. The pain is severe from neck to toes. I can understand why people in pain would rather be dead.
irma
12 May 2009, 20:57
HI I AM IRMA AND I AM SICK FOUR YEARS AND I HATE IT I AM GOING TO MANY DOCTES AND I FEEL THE SAME
Diane
18 Apr 2009, 17:18
I have PSA and Fibro- fatigue is my biggest enemy. I have found out that I can only work out in the evenings and then i do group work outs because I need that push of someone going with me and the group is my social time. I kill to birds with one stone!

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