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What are the best treatments for Relapsing Polychondritis?

See the best treatments for Relapsing Polychondritis here

Relapsing Polychondritis treatments
18 answers
Prednisone, methotrexate and Plaquenil

Posted Apr 26, 2017 by Freya 1000
Steroids in the short term. Then a disease modtfying drug such as methotrexate
Relapsing Polychondritis does not have a cure but it can often be well controlled with medication.

Disease-modifying anti rheumatic drugs like Methotrexate and Prednisolone (Corticosteroids) are often given to suppress the immune system. For milder cases of the condition, non-steroidal, anti-inflammatory drugs and painkillers may be prescribed.

Where the airways are involved, surgery may be required to repair the windpipe (trachea) or stenting to keep the airway open.

Posted Apr 27, 2017 by Lisa Matthews (Lissy) 4800
Out of my own experience biologics have helped a lot but still sometimes cortizone is a must. Many other meds can be used in combination.

Posted Apr 27, 2017 by Laoura 2050
High dose prednisone during a flare. Methotrexate, cyclophosphamide

Posted Aug 9, 2017 by Louise C 1450
In the beginning I believe it's a good idea to try ibuprofen & other NSAIDS then if that does not help decrease symptoms, most likely moving on to steroids as usually destruction is occurring throughout the body & needs to get under control.

Posted Aug 14, 2017 by Susan 2000
So far for me nothing has worked like Prednisone.

Posted Sep 1, 2017 by Diane 2050
Oral steroids, clean diet, immunosuppressants. LDN

Posted Jun 11, 2019 by [email protected] 1000
Prednisone and methotrexate

Posted Jun 12, 2019 by Tmrcarlson 3550
Methotrexate, imuran, cellcept, humira, remicade, Rituximab, cytoxan are some of the most common. Also anti inflammatory medication like Celebrex, colchicine, mobic etc
Prednisone is commonly used for relapsing polychondritis and for most assists in controlling flares in high doses. Some remain on a maintenance dose in combination with other drugs as above and at times increase dosages to control flares.

Posted Jun 12, 2019 by Kaz 3000
Immunosuppressants
Steroids
Biologics

Posted Dec 30, 2019 by Leanne 2500
Steroid medications, DMARDs, anti inflammatory medications, biologics, pain relief

Posted Dec 30, 2019 by Carrie 3050
dapsone and colchicine quiet symptoms. Currently taking infusions of zolair.

Posted Mar 20, 2022 by shlawver 2500
Actemra helps me so much. Its better than steroids outside of a few severe flairs.FIGHTING MEDICARE FOR INJECTOR PEN SO INFUSION WILL NOT BE NEEDED.

Posted Apr 16, 2022 by Dee 100
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Up to now has not how to evaluate the treatments, they are all the cortisone, and we all know what effects this treatment brings us...

Posted Oct 1, 2017 by Ana Luiza Bottura 2000
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Immunomodulatory treatments

Posted Oct 2, 2017 by cmomo 600
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I realize that the most used are corticosteroids, biological and Metrotexato.

Posted Oct 2, 2017 by Glaucia 1800
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Immunosuppressive and corticodes.

Posted Oct 2, 2017 by Carolina 300
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For the time methotrexate, but my I keep getting outbreaks very often.
Short-term corticosteroids

Posted Oct 2, 2017 by Sandra 950

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World map of Relapsing Polychondritis

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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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