9

What is the life expectancy of someone with Relapsing Polychondritis?

Life expectancy of people with Relapsing Polychondritis and recent progresses and researches in Relapsing Polychondritis

Relapsing Polychondritis life expectancy
16 answers
It depends on the are being affected. If your trachea is affected you could die if you don't get to the hospital in time. It can affect your heart as well and any other organs. No one knows how long we will live.

Posted Apr 26, 2017 by Freya 1000
If given the correct medication and health care there is no reason to believe life expectancy is Any different. Obviously where airways are affected then this is the most life threatening

Posted Apr 27, 2017 by Lisa Matthews (Lissy) 4800
Not sure but taking in consideration the new medicines and bilogics i believe that RP will not be a fatal dicease in the near future.

Posted Apr 27, 2017 by Laoura 2050
No one really knows the answer to this question. There is not enough research to answer this. Medication advancements change things, so who knows. I depends on how an individuals body is coping and what areas are affected.

Posted Aug 9, 2017 by Louise C 1450
I honestly believe something else other than RP may "get me". I didn't believe that when I was younger by the way but being almost 60, I do.

Posted Aug 14, 2017 by Susan 2000
I have no idea. It would depend on the degree of seriousness with your RP and what areas of your body are affected. Of course, the throat is dangerous. That is probably our worst fear.

Posted Sep 1, 2017 by Diane 2050
Not sure. They say 5 years. But I have had this diagnosis for 9 years and doing well.

Posted Jun 11, 2019 by [email protected] 1000
Lessened by 5-10 years with no help. Less by a few years with help

Posted Jun 12, 2019 by Tmrcarlson 3550
The life expectancy is better now than previously reported in research papers as you will read on the internet. The highest risk with Rp is when there is tracheal or heart involvement or organ involvement like kidneys and liver. A lot of people in the support groups have reported having the disease 20+ years.

Posted Jun 12, 2019 by Kaz 3000
I have kidney involvement at age 38, now on 1st transplant, also being affected. The research shows 10 yrs w kidney involvement

Posted Jun 30, 2019 by Missy 100
There is no life expectancy. This disease will wax and wane

Posted Dec 30, 2019 by Leanne 2500
It depends on what area is affected, usually good but if airways are affected it can be more problematic

Posted Dec 30, 2019 by Carrie 3050
If you survive the first three years, you will most likely live 5 to 10. If you survive 15 years, you stand a pretty good chance of 25-35. That said, I have survived 34 since the first relapse. I hope for another 9 years.

Posted Mar 20, 2022 by shlawver 2500
Translated from spanish Improve translation
Some articles that I read, the speech 5-7 years of survival,but in fact no one of this information.
It was all very vague

Posted Oct 2, 2017 by Ana Luiza Bottura 2000
Translated from spanish Improve translation
You can live a long, your life does not change... only now you have to be more cautious with your body

Posted Oct 2, 2017 by Kevin Ochoa 2000
Translated from spanish Improve translation
With new drugs I think the life expectancy is similar to that of any person if there are no complications of the trachea or the heart

Posted Oct 2, 2017 by Sandra 950

Relapsing Polychondritis life expectancy

Celebrities with Relapsing Polychondritis

Celebrities with Relapsing Polychondritis

7 answers
Is Relapsing Polychondritis hereditary?

Is Relapsing Polychondritis hereditary?

15 answers
Is Relapsing Polychondritis contagious?

Is Relapsing Polychondritis contagious?

12 answers
ICD9 and ICD10 codes of Relapsing Polychondritis

ICD10 code of Relapsing Polychondritis and ICD9 code

13 answers
Natural treatment of Relapsing Polychondritis

Is there any natural treatment for Relapsing Polychondritis?

12 answers
Living with Relapsing Polychondritis

Living with Relapsing Polychondritis. How to live with Relapsing Polychondr...

17 answers
Relapsing Polychondritis diet

Relapsing Polychondritis diet. Is there a diet which improves the quality o...

18 answers
History of Relapsing Polychondritis

What is the history of Relapsing Polychondritis?

10 answers

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 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...

Tell your story and help others

Tell my story

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...

Ask a question and get answers from other users.

Ask a question

Find your symptoms soulmates

From now on you can add your symptoms in diseasemaps and find your symptoms soulmates. Symptoms soulmates are people with similar symptoms to you.

Symptoms soulmates

Add your symptoms and discover your soulmates map

Soulmates map