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

Maintaining a romantic relationship while living with relapsing polychondritis is entirely possible, though it requires intentional communication and adjustments to accommodate the unpredictable nature of flare-ups. While relapsing polychondritis presents unique challenges due to pain, fatigue, and potential physical changes, open dialogue and shared coping strategies can foster intimacy and resilience. How does relapsing polychondritis affect intimacy and relationships? The fluctuating nature of relapsing polychondritis, characterized by systemic inflammation and pain, can impact emotional and physical closeness.

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

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Is it easy to find a partner and/or maintain relationship when you have Relapsing Polychondritis?

Relationships and Relapsing Polychondritis: real patients share how diagnosis affected dating and partnership.

Couple and Relapsing Polychondritis

Maintaining a romantic relationship while living with relapsing polychondritis is entirely possible, though it requires intentional communication and adjustments to accommodate the unpredictable nature of flare-ups. While relapsing polychondritis presents unique challenges due to pain, fatigue, and potential physical changes, open dialogue and shared coping strategies can foster intimacy and resilience.



How does relapsing polychondritis affect intimacy and relationships?


The fluctuating nature of relapsing polychondritis, characterized by systemic inflammation and pain, can impact emotional and physical closeness. Chronic pain, joint stiffness, and the side effects of medications like prednisone may decrease libido or make physical touch uncomfortable. It is essential to recognize that relapsing polychondritis is a systemic condition, and your partner’s support is vital for navigating the "new normal" of your physical capabilities.



What communication strategies help when living with relapsing polychondritis?


Honest, ongoing communication is the foundation of a healthy partnership. Consider these strategies to navigate the impact of relapsing polychondritis:



  • Define your limits: Clearly explain how your symptoms, such as vertigo or joint pain, affect your daily capacity.

  • Schedule check-ins: Dedicate time to discuss how the condition is currently affecting your mental and physical health.

  • Collaborative planning: Discuss ways to modify activities during flare-ups to maintain quality time without exacerbating symptoms.



Is relapsing polychondritis hereditary and does it affect family planning?


Current medical literature does not classify relapsing polychondritis as a strictly hereditary condition, though there is ongoing research into genetic predisposition and immune-related links. If you are considering family planning, it is crucial to consult a rheumatologist, as some medications used to treat relapsing polychondritis (such as methotrexate or cyclophosphamide) may need to be adjusted or paused to ensure safety during pregnancy.



When should couples seek professional support?


Chronic illness can place significant strain on any relationship. Couples counseling is recommended if you notice persistent communication breakdowns, feelings of resentment, or if the caregiver is experiencing signs of burnout. A therapist can provide a neutral space to address the emotional toll of relapsing polychondritis and help both partners develop sustainable support systems.



Next steps



  • Join the DiseaseMaps.org community to connect with over 468 members who share lived experiences.

  • Consult your rheumatologist about family planning or intimacy concerns if medications are affecting your health.

  • Seek a therapist experienced in chronic illness to help navigate the emotional complexities of your diagnosis.



Disclaimer: This content is for informational purposes only and does not constitute professional medical advice, diagnosis, or treatment; always consult with your physician regarding your specific health needs.



References



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

  • Orphanet: Portal for rare diseases and orphan drugs

  • PubMed: Clinical reviews on the systemic management of Relapsing Polychondritis

  • DiseaseMaps.org: Community insights and patient-reported outcomes

Author: DiseaseMaps Editorial Team
Reviewed against authoritative medical sources (NIH GARD, Orphanet, OMIM)
Last updated: 2026-05-08
Medical disclaimer: This information does not substitute professional medical advice. Always consult your doctor before making health decisions.
Source: DiseaseMaps.org
12 answers
Yes, I'd say next to impossible however I am still married after over 30 years.

Posted Aug 14, 2017 by Susan 2000
Look for someone who is compassionate. He or she must be able to put you first above everything else. He/she will have to carry the load during the flares. The problem with RP is that we look healthy. It is something you wouldn't see unless you live with a person. Your partner must have a sincere interest in reading and learning about the disease. Otherwise, they may think you are a hypochondriac.

Posted Sep 1, 2017 by Diane 2050
hmmm!!! for me, no! I have had a relationship breakdown due to my health issues. For others though, they have partners that have stood by them.

Posted Mar 20, 2018 by Lisa Matthews (Lissy) 4800
No it's like having cancer your partner needs t have alot of patience and help you alot

Posted Jun 12, 2019 by Tmrcarlson 3550
Relationships can be hard or tested without adding in an autoimmune disease. It’s important to communicate with your partner so that they can support you. Depression and pain can affect how we treat the ones we love and it’s also hard for our partners to watch us suffer in pain and be unable to help. Communication is vital.

Posted Jun 12, 2019 by Kaz 3000
This is a difficult question. It's the same as meeting anyone, however, it takes a patient, understanding and loving person to partner with someone who has serious health issues

Posted Dec 30, 2019 by Leanne 2500
No, it is hard as the illness brings huge challenges, disability, pain and it makes it more difficult and outs huge strain in relationships.

Posted Dec 30, 2019 by Carrie 3050
I had no trouble but I had to eventually replace nose cartilage with irradiated bone.

Posted Mar 20, 2022 by shlawver 2500
Translated from spanish Improve translation
Yes, I have not had a problem with this

Posted Oct 2, 2017 by Ana Luiza Bottura 2000
Translated from spanish Improve translation
If it is difficult, my partner of 6 years of relationship he left me when I started the disease... but not everything is bad after a time, I met whom today is my wife... the world is big and the best people are in difficult times with you...

Posted Oct 2, 2017 by Kevin Ochoa 2000
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Do two years of marriage this month, and my husband has helped me a lot and understood my moments of weakness, because we are human!
So I'm living one day after another with great faith and a strong will to beat this disease.

Posted Oct 2, 2017 by Glaucia 1800

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Stories of Relapsing Polychondritis

RELAPSING POLYCHONDRITIS STORIES
Relapsing Polychondritis stories
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...
Relapsing Polychondritis stories
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...
Relapsing Polychondritis stories
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...
Relapsing Polychondritis stories
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...
Relapsing Polychondritis stories
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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Relapsing Polychondritis forum

RELAPSING POLYCHONDRITIS FORUM
Relapsing Polychondritis forum
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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