Short answer · Medically reviewed summary · Last updated: 2026-05-08

Many individuals living with Relapsing Polychondritis maintain successful careers by balancing medical management with strategic workplace adjustments. Whether or not someone can work depends largely on the severity of their symptoms, the specific organs affected, and the flexibility of their professional environment. Can people with Relapsing Polychondritis maintain a career? Yes, many people with Relapsing Polychondritis continue to work effectively, though the disease's relapsing-remitting nature requires proactive management.

18 people with Relapsing Polychondritis have shared their first-person experience on this question at DiseaseMaps.

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Can people with Relapsing Polychondritis work? What kind of work can they perform?

Can you work with Relapsing Polychondritis? Real patients share what jobs they do and how they adapted, plus practical guidance.

Relapsing Polychondritis jobs

Many individuals living with Relapsing Polychondritis maintain successful careers by balancing medical management with strategic workplace adjustments. Whether or not someone can work depends largely on the severity of their symptoms, the specific organs affected, and the flexibility of their professional environment.



Can people with Relapsing Polychondritis maintain a career?


Yes, many people with Relapsing Polychondritis continue to work effectively, though the disease's relapsing-remitting nature requires proactive management. The ability to work is often determined by the frequency of flares and whether the condition affects critical areas like the airway, which may necessitate more frequent medical leave. With 468 members on DiseaseMaps.org, our community reports that those who prioritize early treatment and symptom control often find they can sustain long-term professional stability.



What types of work are most manageable?


Roles that offer autonomy and physical comfort are generally most sustainable for those with Relapsing Polychondritis. Careers that allow for sedentary tasks or flexible movement are often preferred over high-impact or physically demanding jobs. Consider the following adjustments to optimize your professional life:



  • Remote work or hybrid arrangements: Reduces fatigue associated with commuting.

  • Flexible scheduling: Allows you to attend medical appointments or rest during flare-ups.

  • Ergonomic workstations: Helps minimize joint strain if polyarthritis is a symptom.

  • Climate-controlled environments: Extreme temperatures can sometimes trigger discomfort in those with sensitive cartilage.



How can I communicate with my employer?


Open communication is key to managing Relapsing Polychondritis in the workplace. You are not required to disclose your specific diagnosis, but you may request "reasonable accommodations" under laws like the Americans with Disabilities Act (ADA). Focus your conversation on the functional limitations you face—such as the need for rest breaks or ergonomic support—rather than the clinical details of Relapsing Polychondritis itself.



Next steps



  • Consult with a rheumatologist to develop a treatment plan that minimizes systemic flares.

  • Connect with the 468 members on DiseaseMaps.org to share career management strategies.

  • Contact an occupational therapist to help assess your workspace needs.

  • Review your local labor laws regarding disability accommodations and medical leave.



Medical disclaimer: This content is for informational purposes only and does not constitute professional medical advice, diagnosis, or treatment; always consult with your specialist physician.



References



  • NIH Genetic and Rare Diseases Information Center (GARD): Relapsing Polychondritis.

  • Orphanet: Relapsing Polychondritis (ORPHA: 732).

  • DiseaseMaps.org: Community patient data and resources for Relapsing Polychondritis.

  • The Relapsing Polychondritis Foundation: Patient support and clinical information.

Author: DiseaseMaps Editorial Team
Reviewed against authoritative medical sources (NIH GARD, Orphanet, OMIM)
Last updated: 2026-05-08
Sources cited: NIH Genetic and Rare Diseases Information Center (GARD): Relapsing Polychondritis. · Orphanet: Relapsing Polychondritis (ORPHA: 732). · DiseaseMaps.org: Community patient data and resources for Relapsing Polychondritis. · The Relapsing Polychondritis Foundation: Patient support and clinical information. · WHO
Medical disclaimer: This information does not substitute professional medical advice. Always consult your doctor before making health decisions.
Source: DiseaseMaps.org
19 answers
It depends on the severity of the disease. Some are very debilitated and others my not be as progressed in there disease at the time.

Posted Apr 26, 2017 by Freya 1000
Every person is different and rp affects us in very different ways to varying degrees. Many work still in their normal cateers but many also are on disability benefits.

Posted Apr 27, 2017 by Lisa Matthews (Lissy) 4800
People can work but need to have a work with no stress and adjustable to their condition according to the stage of the condition of each person.

Posted Apr 27, 2017 by Laoura 2050
I think it depends on how severely affected you are and how well your disease is controlled. I am unable to work. My health is not stable enough. I would be very unreliable.

Posted Aug 9, 2017 by Louise C 1450
I think depending on the severity of RP determines if a patient can work or not. For me I had very complex problems & heart surgery so I could not.

Posted Aug 14, 2017 by Susan 2000
No....I don't think we can. The only type of work I think I could do would be something on the computer from home. I try to stay away from crowds of people due to my immune system. However, there are days that I would not be able to type for hours at a time.

I think there are a very small percentage of people with RP who are able to work full time.

Posted Sep 1, 2017 by Diane 2050
I'm still working 3 days a week but it's taking a toll. Im fatigued and the medicine side effects cause me to sweat a lot ( very attractive!) and my electrolytes are all over the place. Its very hard to be taken seriously when you are so unreliable. Brain fog also doesn't help.

Posted Feb 3, 2018 by Barbara 100
Yes they can defiantly work. Doesn’t effect everyone the same.

Posted Jun 11, 2019 by [email protected] 1000
Yes but sitting work and not for long periods

Posted Jun 12, 2019 by Tmrcarlson 3550
For those who have mild or controlled relapsing polychondritis they can usually remain productive in the workplace. However those with severe or uncontrollable relapsing polychondritis find it hard to perform daily tasks and usually cease working. It all depends on the status of the disease and whether other autoimmune conditions are involved. Fatigue is a major part of relapsing polychondritis.

Posted Jun 12, 2019 by Kaz 3000
Yes, they can work as much as their condition allows

Posted Dec 30, 2019 by Leanne 2500
It varies between sufferers and how they are affected by their disease, how effectively their disease responds to treatment and many other factors.

Posted Dec 30, 2019 by Carrie 3050
I taught school for 30 years while suffering relapses. The disease did not affect my cognitive abilities.

Posted Mar 20, 2022 by shlawver 2500
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Depends on how much the disease has affected you.

Posted Oct 1, 2017 by Ana Luiza Bottura 2000
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If you can work in any position. With the exception of jobs that expose you to prolonged time in the sun

Posted Oct 2, 2017 by Kevin Ochoa 2000
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Yes, but only in moments outside of the buds, and probably with a reduced day.

Posted Oct 2, 2017 by cmomo 600
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Depends on what each one can.
In my case working in the kitchen of a restaurant and is a heavy work. For now I am giving an account, even if that sometimes costs me...but I insist not to betray me.

Posted Oct 2, 2017 by Glaucia 1800
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In my case I can't work on anything, I have a lot of pain and tiredness

Posted Oct 2, 2017 by Sandra 950

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The first time I noticed symptoms, I thought I was having an allergic reaction to something at work. My ears became so red and inflamed and hurt so bad. I let it go on for almost 3 days before finally going to a hospital where I was diagnosed with re...
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It began with dry nose, nose bleeding and what my GP thought was a sinus infection. Antibiotics and prednisone perscribed, helped for a while, then reoccurred. Ear then swelled over twice the size - red, shiny and moist, GP again said outer ear infec...
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i had progressively worsening breathing issues for many years before my diagnosis of rp.  I went through many specialists and tests and no one could identify why I was having breathing issues.  I had no outward signs of rp until one day my ears swe...
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I was officially diagnosed with RP 2 yrs ago. No one else in my family has it. It started approximately 5 years ago with ear flares, jumping from one to the other. My PCP happened to go to a conference where RP was discussed, and soon contacted me to...
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I have had strange symptoms before this came to light, but during my last trimester of my pregnancy with my youngest son, I had a severe respiratory infection that never seemed to get better. I have had exercise induced asthma since I was young and t...

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I don't think RP is as rare as we are led to believe. It seems many symptoms are unrelated. You go to an ortho doc for knee/joint pain. You go to an ENT for ears and throat. You go to an ophthalmologist for eyes. You go to a dermatologist for skin. T...

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