Pulmonary Sarcoidosis: How are you dealing with it?
I'm very interested in creating a discussion group with other patients being treated for pulmonary sarcoidosis and how they're dealing with it. I was diagnosed ~ 10 yrs ago and it is unfortunately gradually getting progressively worse spreading from my lungs to other parts of my body. I'm mainly interested in what others have received for a prognosis and most of all how they handle the, at times, somewhat debilitating pain (primarily rib cage) that goes along with it.
Interested in more discussions like this? Go to the Lung Health Support Group.
Welcome @454june3736. Fatigue is a challenge. Will you taper off prednisone? What are the implications of kidney failure? Dialysis?
Thank you Colleen!
I am happy to have found support on Sarcoidosis. Sometimes you feel like the only one.
Yes, I am tapering off prednisone. I will begin 2mg 10/1. After I have tapered completely off,
I will see how my body reacts to not having Prednisone at all. I am praying that my body will do well.
I will have my complete renal blood tests in November and my nephrologist will view them with me. At this point, my kidneys are functioning at 23%. I don't think that I will have to be on dialysis unless my levels get worse.
I had never heard of Sarcoidosis either until last year. It totally turned my world upside down. I was in the hospital for 11 days. It took 3-4 days searching to find out what was going on in my body.
It sure is a journey. I am so glad that your husband is living a regular length life with it in his lungs. I am so sorry to hear about your neighbor.
Thank you for taking the time to share with me and encouraging.
One day at a time 🙂
Yes, one day at a time - and actually that’s the best way to live as we can’t change the past and the future is unknown. And don’t ask why or how you got sarcoid because it will make you crazy! I have MAC and aspergillosis and do what I can and what I can’t I can’t. Blessings , Irene
I find this very interesting because I had a Dr do testing and sent me for a consult with a Sarcoidosis Specialist, but then just left me hanging and never followed up with a final Dx, or non-Dx, just dropped it. But, since then, I have had so many symptoms of Sarcoidosis, including lung nodules and scar tissue on one lower lobe. I have MCI, so can't recall the other symptoms I had right now, but always wondered if I did have Sarcoisodis. I know there were other symptoms that pointed to it, but just can't think of them right now. In my life, just another time that Drs have thrown around Dx's, but then left me hanging. I did finally get the courage to be my own advocate and speak up to the Drs, but this was after that episode. I am curious if you are on oxygen because of oxygenation issues? I have developed these issues since about 2019 and still continue to deal with oxygenation "dips" all the time, even into the upper 70s. But, again, Drs have failed me! LOL! Are oxygenation rate issues related to Sarcoidosis? Just wondering. Thank you for sharing. Your post really sparked my interest.
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Hello. Curious how they found granulomas in your kidneys ? Did you have symptoms and then a kidney scan.?
I have not been on prednisone yet but since I was tested for everything else and all is negative, I assume it is just inflamation that prednisone would help
Hope you are doing better now
Did the castor oil packs continue to help? How long did you continue doing them?