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Relapsing Polychondritis and depression

Can Relapsing Polychondritis cause depression? Could it affect your mood? Find out how Relapsing Polychondritis can affect your mood.

Relapsing Polychondritis and depression
6 answers
Yes, RP can be hard to deal with and the medications also dont help. If we are on steroids that can cause mood changes also. For me the hardest thing is not being able to do the things I want to do, or be as active..

Posted Mar 20, 2018 by Lisa Matthews (Lissy) 4800
Causes depression because its painful and life threatening

Posted Jun 12, 2019 by Tmrcarlson 3550
Relapsing polychondritis can cause depression. The constant pain, frustration of dealing with doctors not knowledgeable in the condition, the way it can affect relationships, not being able to exercise or work. The change in body size due to medications, the loss of hair due to medications. A number of factors contribute to depression. Finding a psychologist can help with depression and also having a support group who can support you and understand how you are feeling helps. Having family and friends who understand your condition and support you helps. Finding activities or hobbies helps also.

Posted Jun 13, 2019 by Kaz 3000
Relapsing polychondritis can cause depression in some patients due to the pain and fatigue. Also, having a rare disease us difficult when most people have never heard of it, and have no idea how much you suffer. It's depressing when you suffer so much, and some doctors dismiss you.

Posted Dec 30, 2019 by Leanne 2500
Yes, it can lead to depression as can any chronic long term health difficulty, it knowing from one hour to the. Ext how you will feel, having basic functions disappear, being in severe chronic pain would be hard for everyone

Posted Dec 30, 2019 by Carrie 3050
Yes. Depression is triggered by the exhaustion and disabilities that come into play. I have strong religious involvement in a church which gives me hope to climb out of the occasional depressive moods. That focus on good gives me hope that the depression will end soon. Sometimes I just ignore it and do what is needed anyway. Sometimes I rely on a safety list [eat a whole pint of Haagan Daas in one sitting] whatever

Posted Mar 21, 2022 by shlawver 2500

Relapsing Polychondritis and depression

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World map of Relapsing Polychondritis

Find people with Relapsing Polychondritis through the map. Connect with them and share experiences. Join the Relapsing Polychondritis community.

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 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...
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...

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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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