Fibromyalgia and Mobility Problems – How to Keep Moving

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Discussing fibromyalgia and mobility problems is apparently taboo.

Only one of my physicians have addressed the subject of mobility and it was only because I brought it up.

Then there are the opinions of the general public, and unfortunately, some fellow fibro warriors, who make those who need to use a mobility aid out to be weak or say we have given up. However, as I have stated time and time again, there is nothing wrong with a fibromyalgia patient utilizing various types of mobility aids.

The sad and funny thing about it is that nobody questions my use of mobility aids when I state it is for arthritis. But their eyes roll if I mention fibromyalgia. The worst part is that we are the only ones who suffer when we refuse assistance.

But what about your thoughts or needs? We need to stop feeling that mobility issues are only important if they are permanent or acknowledged first by others. Acknowledging areas where we are struggling helps to identify what needs to be modified.

I was diagnosed with fibromyalgia in 2003. Since then, I have made many mistakes. And not just little ones! Refusing to accept my physical limitations have landed me in the hospital. It has stolen precious time that could have been spent with family.

The good news is that I have also learned from those mistakes.

Today I am going to load you up with information about how fibromyalgia affects mobility, empower you with tips for sharing your needs, and encourage you to let go of destructive misconceptions.

Because of my chronic illness, fibromyalgia, I have less energy and strength to do what I used to. By using a mobility aid at the grocery store allows me to do more at home!


Disclaimer: This blog post contains affiliate links. I may earn a small commission to fund my coffee-drinking habit if you use these links to make a purchase. You will not be charged extra, and you’ll keep me supplied with caffeine. It’s a win for everyone.


Types of Fibromyalgia Mobility Problems

Fibromyalgia is more than physical pain and fatigue. Muscle pain and weakness can make it difficult to walk and stand. Fatigue and nerve pain may affect balance.

Fibromyalgia symptoms cause physical stress. Our bodies have to work harder to do what used to come easy.

One mistake I made early on was pushing my body to do what I wanted instead of following its lead. My body completely freaked out and began mimicking stroke symptoms. After a week in the hospital, tests revealed nothing, and the incident was diagnosed as a severe flare.

Another mistake I made was walking and standing longer than my body was able to just to give friends and family the impression that I was just like them. This caused my back and neck muscles to seize and freeze. Had I obeyed my body, I wouldn’t have had to spend six months on my back. Six months that should have been spent enjoying time with friends and family were spent on the couch with heavy-duty muscle relaxers and heat/ice, and massage therapy.


Frozen muscles, dizziness, fatigue, and widespread pain limit mobility. If you are unable to walk as far as you used to, experience additional pain after walking or standing for an average amount of time, or fall often, it is safe to assume that fibromyalgia has affected your mobility.

My fibromyalgia issues with balance have led to a broken tailbone, toe, and many bruised bones. Each injury increased my medical expenses and decreased my productivity.

If grocery shopping feels like a form of torture, fibromyalgia has affected your mobility.


When and How to Discuss Your Fibromyalgia MobilityProblems

Before we begin, I want to make it clear that you do NOT have to discuss our mobility issues with anyone. Your health, abilities, and disabilities are nobody’s business. With that said, you should always discuss them with your physician.

Never hesitate to discuss new or continuing mobility issues with your doctors. Doing so helps them understand how your chronic illness is affecting your body. It may also bring to light other health issues that may have been overshadowed by your fibromyalgia diagnosis. When talking with your physician, be sure to emphasize the impact your mobility issues are having on your life.


When it comes to friends and family, it is best to inform those you consider as part of your support team. This will help them know how to help you. Be honest; it is okay to share your frustration over what is happening with your body. Be real when discussing your mobility options.

As for the rest of the world, it is none of their business. With that said, should you use a mobility aid, be prepared to be asked. Because society makes people feel that mobility aids are only for those with an injury or disability that affects the legs, it is easy to feel like we need to defend ourselves. But you do not need to.

If you do choose to offer an explanation, keep your calm. Don’t tell people to f*c& off; talk in a relaxed manner. Give a simple explanation and move on.


Ways to Keep Moving

Wheelchairs are the first thing people often think of when they hear the term mobility aid. But that is only one mobility option.

Options for balance issues include canes, walking sticks, and rollators. When my daughter was younger, her stroller served as my mobility aid. Pushing it helped with balance and the basket to put my bags in, taking pressure off of my shoulders and back. Dog strollers are another great tool.


One of my favorite mobility aids is my rollator/transport chair combo. It allows me to walk, provides a place to rest my feet and back, and gives my entire body a break when in transport chair mode. While my family feels it is not as easy to push as my manual wheelchair, we agree that when my need to be pushed is limited, it is the best tool to use.

Power chairs are a wonderful option for those who have had their mobility compromised yet want to remain independent.

The most important thing anyone with fibromyalgia can do to keep moving is to listen to their body. Pacing and not exceeding your body’s boundaries will allow you to do more regularly. Pushing hard and continually running yourself into the ground is guaranteed to decrease your productivity, plus time and ability to do the things you enjoy with the people you love.

Zipr Mobility Solutions - Power wheelchairs and scooters

How to Know When Your Fibromyalgia Mobility Problems Require the Use of a Mobility Aid

Many people wait until they can’t do anything before they consider using a mobility aid. In the meantime, they miss out on so much living!

Signs that it may be time for you to use a mobility aid include but are not limited to:

  • Falling often
  • Not enough energy to complete simple tasks
  • More time is being spent in bed
  • Going out less
  • Growing more dependent on others
  • Pain after simple physical activities
  • Missing out on family events
  • Fear of pain that will occur if you leave the house

Choosing a mobility aid can be overwhelming. Lucky for you, I wrote an article to help you find one that fits your needs, budget, and lifestyle. Read it here!

Improving life with chronic pain should never be a taboo subject! Talking about fibromyalgia mobility problems helps us prepare for the future, no matter what it holds.

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The Disabled Diva, Cynthia Covert is a 2020 WEGO Health Award Finalist for the category of Best in Show Blog.

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Published by Cynthia Covert

Diagnosed in 2001 with psoriasis, followed by fibromyalgia, psoriatic arthritis, endometriosis, and later a botched hysterectomy turned her world upside down. Cynthia shares her experience, advice, and tips for how to make life with chronic pain easier and less painful.

14 thoughts on “Fibromyalgia and Mobility Problems – How to Keep Moving

  1. I use a wheelchair full time now. Fibromyalgia came quick and has progressed just as quickly. I have a great deal of problem climbing steps. We just moved and there are 2 steps in and out and I can’t maneuver them. I’m stuck inside. Looking a ramps to help.

  2. I’ve lived with Fibromyalgia for 30 years the last two years I’ve had to start using walls and furniture to be able to move around on my bad days. I’ve had some incidents when I would be walking my pup and I’d fall when this happened I had to crawl to the nearest post or tree just to be able to get backup again. When I fall I need aid to get backup if I’m down on my knees to clean the floor I need the aid of chairs, walls, counters anything to help me get up.

    1. Hugs!! If you haven’t already, be sure to talk to your doctor about this development. You never know if something else is at play. I have been wobbly since diagnosis, but my symptoms were also already severe by the time I shared them with my doctor.

  3. It’s been awhile since you wrote but you forgot my favorite mobility aid! I have a service dog. She helps me balance, walk at an easy pace, I lean on her to get up and she pulls me upstairs. Those are just the physical help she gives. She gets me moving in the morning, keeps me calm when I am so foggy and start to panic, reminds me to take my meds and is just a good friend when I’m feeling down. I did most of the training myself and paid to have her tested and registered. People do ask questions but mostly they ask about my beautiful dog.
    Thanks for the info!

  4. Problems with mobility was what made me decide to lose a load of weight. I’m on a mission to lose 100lb and so far I’ve lost about 44lb. The weird thing is, whilst I can definitely feel the benefit of the lessening weight on my already encumbered limbs, it also made me realise what pains/aches etc really will always be with me and those which were probably caused/exacerbated by the excess weight. And what really surprised me, was just how many new aches & pains I’d feel as the weight lost seemed to remove some of the actual support that was holding me up. I’m having to reevaluate all my range of movement and figure out new ways to hold myself and measure out my energy, so as not to trigger a proper flare-up. I want to be able to put off needing mobility aids for as long as possible, but I’m not stupid; I know this is a progressive condition and things will get worse over time. I just want to try and do as much as I can with weight loss and nutrition, to hold that off for as long as I can. Not because I’m ashamed of being ill or worried about being seen with a cane or anything like that, but because I really just want to have as much of an active life as I possibly can, before the inevitable slows me down even more. Thank you for such a well written post!

  5. I’m getting closer to needing help. I and my chiro think I’m getting arthritis in my hips and I used to fall quite a bit before I began seeing her. I’m doing better now thank heavens. I am a merchandiser and have learned what my limits are and how long I can work at a time. My stores are all within 5 miles or so and I can work and then go home and rest and then head out to the next store in the evening if I need to. Sometimes I need to if I’m not sleeping well or not feeling well. Usually I’m ok once I get moving but when I’m sitting or take a break for any length of time I stiffen up so I cant walk very well. I’m considering a cane to keep in my car for getting from the car to the house or into my job and for getting up from the bed to the bathroom if its needed. I use a heated mattress pad and that has helped a lot at night. I have a friend keeping an eye out for a walker that has a seat on it. I’m hoping it will fold up and store under my bed until I need it in the future. It’s also getting harder and harder for me to clean. I’m not sure how I’m going to deal with the future. I’m single, no insurance & no dr anymore (she has retired). Right now my current chiro specializes in some therapies I need (trigger point/myofascile release) and I feel like that is all that’s keeping me working and moving.

    1. Hugs!! That’s a lot to deal with. Walkers are great not just for balance and a place to sit when needed, but for lightening your load when you have heavier things to carry. For example, my back and shoulders would never put up with my lugging a backpack around Disneyland. With my walker, I prevent falls and have a place for my heavy bag. My first walker did not fold well. Even folded, it took up a lot of space. But the one I purchased last year folds flat and has been a godsend. I wrote about it here:

      I hope you find what you need and that you can continue doing what you love.

  6. I know that in reality I’m getting close to the need for a wheelchair, but I’m doing everything I can to stay fairly mobile without overdoing it, using pain meds and trying to delay it for as long as possible. I do typically use a stick now when I go out and yep, there are definitely looks and questions and you have to develop that harder outer shell where you can ignore the looks and push past it. “As for the rest of the world, it is none of their business” < Absolutely. It's awful to think that so many are so cynical and ignorant when it comes to fibro, too. It can be incredibly debilitating, with or without other conditions this arthritis or nerve damage. Excellent post, Cynthia! xx

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