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Is there any natural treatment for Relapsing Polychondritis?

Are there natural treatment(s) that may improve the quality of life of people with Relapsing Polychondritis? Here you can see if there is any natural remedy and/or treatment that can help people with Relapsing Polychondritis

Natural treatment of Relapsing Polychondritis
12 answers
No natural treatments available in my opinion.

Posted Aug 9, 2017 by Louise C 1450
I've tried many other treatments from Chinese Medicine to Acupuncture to Chiropractic which all offered me good results.

Posted Aug 14, 2017 by Susan 2000
If there is anything natural, I would think it would be to eat organic foods. God didn't intend for us to eat a lot of the stuff we do today. I believe You Are What You Eat is very true!!

Posted Sep 1, 2017 by Diane 2050
debatable... there are reports on the internet about curing RP with a vegan diet! However, I was actually vegan for three years before my diagnosis and it didn't stop my trachea narrowing dangerously.

However, certain diets do help relieve symptoms and inflammation and many patients with RP do use alternative and holistic, and natural remedies to help them in their day to day living with RP.

Posted Mar 20, 2018 by Lisa Matthews (Lissy) 4800
Try to exercise not much but as possible. Keep calm and avoid stress

Posted Jun 12, 2019 by Laoura 2050
Not as far as I know

Posted Jun 12, 2019 by Tmrcarlson 3550
I am unaware of any natural remedies for relapsing polychondritis. Some have advised in the support groups that following an autoimmune diet protocol have helped their flares. There is no known cure for relapsing polychondritis.

Posted Jun 12, 2019 by Kaz 3000
No, however, some people follow a vegan diet, some people find that cbd oil helps.

Posted Dec 30, 2019 by Leanne 2500
Many folk like to try various natural relief, but it is a very individual choice.

Posted Dec 30, 2019 by Carrie 3050
Not in my case. However, I suppose some focus on wellness which would be a safety factor from the depression.

Posted Mar 20, 2022 by shlawver 2500
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Unfortunately not, I'm unaware of

Posted Oct 2, 2017 by Ana Luiza Bottura 2000
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I don't know of any treatment naturist... although I have heard that cleanse the blood of all the medicine is swallowed the body is a good thing, it made with this type of treatment...

Posted Oct 2, 2017 by Kevin Ochoa 2000

Natural treatment of Relapsing Polychondritis

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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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