What is Fibromyalgia
Fibromyalgia (FM or FMS or Fibro) is a debilitating chronic syndrome (constellation of signs and symptoms) characterized by diffuse or specific muscle, joint, or bone pain, fatigue...
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Fibromyalgia (FM or FMS or Fibro) is a debilitating chronic syndrome (constellation of signs and symptoms) characterized by diffuse or specific muscle, joint, or bone pain, fatigue...

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Can you exercise?
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Here is a link to a "news" article published today....I do not know the credibility of this source.
It challenges me to be thinking about this - I don't like pain! And I tend to curl up and wait for it to go away. There are valid reasons for that -- I have other medical conditions along with the fibro...and the wrong activity can also be bad for my other condition and cause it to flare. It does feel good to do some kind of movement though. So - I share this article below for your thoughts...and recommendations...? How much do you exercise? How many times a week? What is good for us? Because over doing can really be a set back! I don't want to make an excuse - I just really want to be wise....and this is a tricky area for me...and confusing - so thought I'd ask what you all think? Here is the link: http://mychannelnews.info/fibromya... And the article published today: Sunday, November 15th, 2009 Fibromyalgia and Loss of Muscle Tone – Can Exercise Really Help? Fibromyalgia is a condition that can cause intense and sometimes unabating pain all over the body. For this reason many patients afflicted with the disorder find it difficult to complete their everyday activities, let alone consider an exercise regimen. However, according to experts in the field, one of the lesser addressed problems faced by those with fibromyalgia is muscle wastage because they are rendered far more inactive than in the past, or others their age might be. Therefore many doctors who treat fibromyalgia patients recommend that they strive to complete at least some low impact, gentle exercises to keep and even improve their overall muscle tone. The key to success is to undertake workouts gently, in moderation and to exercise as much patience as possible. The pain and fatigue that fibromyalgia patients suffer from can worsen without warning. There may be days when exercise is simply impossibility, and the best course of action is to listen to the body. Other days may find a patient able to complete only those exercises that see them lying on the floor or sitting. The important part is to keep trying to the best of one’s ability. Stretching is important, as part of the pain may come from muscles lying dormant all day, stiffening and protesting as they do so. Making a few simple stretching exercises a part of their daily routine has helped many fibromyalgia feel at least a little better. Some people also recommend yoga both for its physical benefits and the sense of relaxation it imparts. To try to strengthen the muscles light free weights can be very helpful. Two pound weights are not too heavy but will still provide good resistance without overstressing the muscles. There are a number of good exercise regimes on the Internet that can be adapted to fit the constraints of a person with fibromyalgia. It is important to begin with just a few repetitions a day, only increasing them as can be tolerated. Other people with fibromyalgia have had great success following a well tailored Pilates regime, one of the goals of which is to improve muscle tone in everybody who practices the art. As important as the exercise regime undertaken by fibromyalgia patients to increase muscle tone is the diet that they follow. An adequate amount of protein is essential and most medical practitioners suggest that fibromyalgia patients avoid caffeine and alcohol wherever possible. Whatever exercise regimen a fibromyalgia patient chooses to undertake the key is patience and perseverance. As their body becomes more used to exercise again patients will discover for themselves where their strengths and weaknesses lie and retool their fitness program to compensate for them. Posted on 11/15/09, 05:11 pm |
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I try to get some form of exercise each day, whether it is some walking, stretching, strength training or water aerobics. Fatigue is my biggest problem these days and if I overdo it, it will be worse the next day.
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I walk, I swim, I dance...mostly More because of my vascular disease...but this movement SURE Helps with my FM...also Keeps Depression & Anxiety at arms length...YeaY !!
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No......... I cannot exercise. I'm gonna have to start though, slow and steady.
I did treatment for hep c and in combination with the fibro it wore me out and made me weak. I was bedridden for about 6 months and have not been able to bounce back.
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Nice to see a well-balanced article that recognizes that fibro patients need to listen to their bodies' rather than try to keep up with non-fibro people.
I also have chronic myofascial pain with huge trigger points in my lower legs that had made to the point I can only walk for exercise lest I be in too much pain. I exercised diligently for years and years before being diagnosed and am probably worse off for it. It took me a long time to learn to listen to my body as hubby keep urging me to.
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Good article.
I find my exercise capabilities come and go. For awhile there I was hiking and canoeing every weekend, working out in a gym 4-5 days per week. Good times. I'm having a bad season right now. It's been going on for about a year or so. I exercise throughout the day - mostly just stretches but also leg lifts while I'm waiting for water to boil, marching as I put away laundry. I have some free weights I keep around and use them when I'm up to a little more movement. I'm very aware of how little I'm moving these days. I think it's harmful to my body but if I overdo, I'm sunk. I guess we just do what we can, when we can.
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I recently joined a gym and the few times I have gone to the gym have not affected my fibro. The soreness I felt the next day was directly connected to the workout and not the fibro. I feel so much better after I exercise. I believe it is also a case of doing light cardio before weight training which will bring oxygen to the muscle through blood flow. I stretch lightly before and after exercise.
I also walk a lot. I find when I do not move around too much, those are the days my fibro bothers me the most.
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I don't really exercise very much, but I didn't do that much before I got sick either. But considering my job requires me to be on my feet 30+ hours a week and I have to walk so much since I don't have a car etc...I guess I do exercise. I do tend to restrict what I do when I can....and rest alot. *shrugs* 29 going on 80
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Exercise makes me physically ill and I pay dearly for it later.
If you have CFS with your FM you should be extremely careful. Friday, October 30, 2009 Dr. Lerner on CFS, Exercise & the Heart http://chronicfatigue.about.com/b/... (note, visit this link if you want to be able to "click through" live links embedded in the article) Chronic Fatigue Syndrome, Exercise & the Heart Dr. A. Martin Lerner: Protecting the Heart Friday October 30, 2009 by Adrienne Dellwo When it comes to chronic fatigue syndrome (CFS or ME/CFS), exercise is a contentious subject. That's because of a symptom called post-exertional malaise; exertion makes symptoms worse. Still, some doctors, researchers, and official organizations recommend graded exercise therapy (GET) as a front-line treatment for the condition -- sometimes ignoring all other treatment options other than possibly cognitive behavioral therapy (CBT). Some people say GET has worked for them, while others say they've been made worse by it. Dr. A. Martin Lerner, an infectious disease specialist who himself recovered from ME/CFS, says anything that raises the heart rate of someone with this condition is dangerous, unless they're well on their way to recovery (at a 7 on his EIPS chart.) He says this is because, in his practice, he's seen that ME/CFS does involve the heart. Dr. Lerner says people with ME/CFS have a rapid heart rate when they're at rest, on top of low blood volume. As the disease progresses, he says, the heart muscle becomes weaker. Dr. Lerner has published studies about an abnormal heart function in people with ME/CFS, showing dysfunction even at normal daily levels of exertion, abnormal movement both at rest and under stress, and T-wave abnormalities distinct enough to provide a diagnosis. To check for those heart problem in his practice, Dr. Lerner uses ECG (electrocardiogram) and a Holter monitor (a portable monitor you may wear for a couple of days.) For those in the early stages of recovery, Dr. Lerner says, "Certainly, it is helpful to not just let the muscles atrophy, but sitting up is actually a muscular activity." He adds, "Walk, live, but no exercise until you're at a 7, because if you exercise before that you're going to go backwards." When it comes to gentle exercise that doesn't raise the heart rate, Dr. Lerner seemed fairly neutral, and I spoke to one of his patients who says he did grudgingly OK yoga for her even though she's nowhere near a 7 on the scale. However, she's careful not to do anything that will raise her heart rate. So should you follow some doctors' recommendations to exercise, or heed Dr. Lerner's warnings about cardiac problems? That's a tough question, especially since most doctors wouldn't know what to look for on tests even if they agreed to perform them. Dr. Lerner recommends acquainting doctors with the published, peer-reviewed work done by him and others. If you go to pubmed.gov and type in Lerner AM cardiac, you'll get a list of research abstracts to take to your doctor. You'll also find information on some of Dr. Lerner's heart-related work on his website: Treatment Center for Chronic Fatigue Syndrome. I know -- a lot of doctors will never take the time to educate themselves on this. Here's my idea: start keeping a record of your resting heart rate. If it's high (more than 100 beats per minute), talk to your doctor about the possibility of heart problems. At least that's something that usually gets their attention! Your test results could help you make some very important decisions.
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wow that was a well written article. I myself find that if I work out at all I am dang near bedridden the next day although I can and do stretch every day. I used to teach aerobics and weightlifting for women20 years ago, they always said work through the burn. I don't have the strength or the desire to push thru the pain anymore. I think that is for the youngsters..........................................................................Peg
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