Working with fibromyalgia: what you need to know
Fibromyalgia affects people in different ways and to varying degrees. Some people manage their symptoms well enough to continue working without major disruption. Others find that the condition makes holding down a job extremely difficult, particularly during periods when symptoms worsen.
The severity of fibromyalgia can range from mild discomfort to widespread pain that interferes with most daily activities. Where you fall on this scale will largely determine how much your working life is affected, though this can change over time.
Mild to moderate fibromyalgia and employment
If your symptoms sit at the milder end of the spectrum, you may find that work remains manageable most of the time. Flare ups, when pain and fatigue increase, are common, though how much these affect your ability to work varies considerably from person to person.
Many people with mild or moderate fibromyalgia continue in full time or part time employment. Medication prescribed by your GP can help manage pain and related symptoms such as poor sleep or low mood, though effectiveness varies between individuals and some people experience side effects that limit what they can take. Finding a treatment approach that helps you is worth pursuing, but it does not guarantee that work will become straightforward.
Self-care strategies can also play a role. Stress management, gentle exercise where tolerable, and attention to sleep patterns may help some people alongside medical treatment, though results differ.
It often helps to be open with your employer about your condition. You do not have to share every detail, but letting them know you have a health condition that causes occasional difficulties can make it easier to ask for adjustments when you need them.

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Severe fibromyalgia can make everyday tasks exhausting. Getting through a working day may feel impossible at times, especially if your job involves physical activity, long hours, or high levels of concentration.
If you fall into this category, your GP may refer you to a specialist or a pain management clinic, depending on their assessment and what services are available locally. These services can offer support beyond medication, including physiotherapy, psychological support, and advice on pacing your activities. However, access to such services varies across the NHS, and waiting times can be significant in some areas.
Some people with severe symptoms find they need to reduce their hours, change roles, or stop working altogether. This is a personal decision that depends on your circumstances, the nature of your work, and how your symptoms respond to treatment over time.
Your situation may be slightly different. ask a question below ↓ and our editorial team will reply with our advice.
Workplace rights and support
Under the Equality Act 2010, fibromyalgia may qualify as a disability if it has a substantial and long term effect on your ability to carry out normal daily activities. This means your employer has a legal duty to make reasonable adjustments to help you do your job.
Reasonable adjustments might include:
- Flexible working hours or the option to work from home
- More frequent breaks during the day
- Adjustments to your workstation or equipment
- Changes to your duties during flare ups
- A phased return to work after a period of absence
The Access to Work scheme, run by the Department for Work and Pensions, can provide practical support and funding for adjustments that go beyond what your employer would normally be expected to provide. The scheme requires an assessment, and approval depends on your specific circumstances and the assessor's recommendations. You can find details and apply through GOV.UK.
If you are unable to work, you may be able to claim benefits such as Personal Independence Payment or Employment and Support Allowance. These require assessments, and not everyone who applies will qualify. The application process can be lengthy and complex. Check GOV.UK for current rates and eligibility criteria, or speak to a welfare adviser at your local Citizens Advice for help with applications.
Finding what works for you
There is no single answer to whether you can work with fibromyalgia. It depends on the severity of your symptoms, the type of work you do, and the support available to you. Because fibromyalgia symptoms fluctuate, your capacity to work may also change over time.
Speaking to your GP is a sensible first step if you are struggling. They can review your treatment, consider referral to specialist services where appropriate, and provide evidence if you need to apply for benefits or request adjustments at work. Occupational health services, where available through your employer, can also help bridge the gap between your health needs and your job requirements.
Whatever your situation, support is available, and taking time to understand your options can help you make decisions that suit your circumstances.
Does anypne know who to go to for advice as im so concerned at the moment. It doesnt help im new to it all and have noone to talk to.
I count my blessings because I know some sufferers dont have the support I've had yet I have reached the point where I question the desirability of continuing to go on, feeling like this. I will soon have to make a decision to remain in work or take a leap into the unknown and leave. Very scary.... I wonder often how I came to land up like this..... but like Pandoras box - there is always hope....
I've been diagnosed since Dec 2018 with fibromyalgia after a 13 year fight for a diagnosis for my chronic pain and fatigue (I was diagnosed with Hypermobility Syndrome and IBS and CFS, so knew there was something underlying) I am struggling to hold down my job, having been sacked and on disciplinary in previous positions for absences and again being a step before a disciplinary. I don't know where to go from here. My doctor wont give me painkillers and is wanting to treat me with just anti depressants. I am at my wits end. I'd really appreciate any advice.
The trouble is I haven't had luck with employers, most of last year I was temping anyway and so was able to rest in between assignments having recently left a job of 8 years because of bullying and wanting more hours (the pain wasn't as severe as now) I had to leave my recent employment because they wanted a medical report from my GP and having just had an operation on my womb were less than sympathetic about that or the pain I was experiencing. I was a full time receptionist but this was a role which had me working on a desk hand built for people who were tall or not seated it was too high for me. The stool I sat on wasn't comfortable and requested arms for it so I could actually sit on the damn thing. I was expected to carry heavy items, rush around, walk, run upstairs and it was all getting too much. I actually walked out after receiving a horrible email for the HR manager which suggested to me that they didn't necessarily believe me. I walked out. I also suffer oral Lichen Planus which flares up with the fybro flareup and I have had issues with osteoarthritis (partial knee replacement right knee 2015 and left knee clean out 2017)
My dilemma at the moment is money as is for most people. I have applied for benefits have an understanding Husband to a degree but it is hard for him to understand, and I have just applied for a part-time reception position but have been honest about my health.
Really feel quite lost, the brain is working til I feel tired, but I need to earn money!!!
Anyone have any advise?
Thanks, Jody
Just don't know what to do. Crawling to work. In tears most of everyday. How will I pay my mortgage? Where do I start? Sympathetic and wonderful gp.
So scared of not being able to work. But don't know what to do!!
I have set up a page on facebook. Fibromyalgia won't be me.
I am a chef by trade and have worked hard to climb the ladder in a mostly male dominated profession. it goes without saying that my job is very physically challenging. I first went to a specialist hand surgeon when I experienced overwhelming pain in my hands and wrists and would get the shakes when icing elaborate wedding cake. I was also dropping things a lot. I was told I had carpel tunnel syndrome and went for the opp. Nothing changed afterwards except that my hands were not as strong and my fine motor skills left a lot to be desired. I went to get a second opinion and was then asked to take off my shoes so he could see my feet, and then my knees. He asked how long I'd had pain in these joints. Chefs stand for 12 to 16 hours a day and I was well used to the pain so I had learned to live with it. That is when I was diagnosed but he said I'd had it for at least 4 years already.
I find that having a strong mind set is vital! For me I cannot entertain the thought of pain in the morning. I just accept that its there, do the best I can on the day, and don't beat myself up for leaving things undone or choosing to go to bed early instead of going out with friends.
What I am struggling with though, is that all my training and experience is in food. I now need to look for a less physical job as my condition deteriorates but I am qualified for nothing else. We do not have a grant system in South Africa so I have to work to support myself. (I am single)
Can anyone shed some light on a career path that starts paying the bills from day one but that is not as taxing?
I have tried teaching, but those jobs are like hens teeth and still require you to be physical for at least 8 hours a day.
I am writing a cook book in the hopes that it will be published but that does not bring in money straight away either which I need as my medical bills are a sixth of what I currently earn.
Lastly may I just quickly add that good supportive shoes, and long hot baths steeped in Epsom salts have really helped for the pain when the painkillers and anti inflammatories don't seem to be doing their job. I have also made a helpful mind switch which keeps me motivated. I am not my diseases. I am more than just symptoms. I am first and foremost still the happy, fun-loving, creative and hard working person I have always been. I just happen to also have 3 auto immune diseases.
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