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.
@riverotter, I am just now seeing and reading your post. Thank you for reaching out in this discussion with your questions.
I see that @estrada53 has already responded with some expert knowledge from her own experience. I received my liver and kidney transplant at Mayo Rochester in 2009. I also love the outdoors and hiking. And I have a beautiful granddaughter to love and who blesses my life with her hugs.
How are you doing? Are you being considered for a transplant?
I have had sarcoidosis for over 20 years. The first 5 or so was very. I went to work and bed. And sometimes slept at my desk. I've been exercising for 5 years, try to eat healthy. I have good days and bad. I do go to Mayo and very happy I do. They take time for you and are very knowledgeable. My test are shown to me and explained. Thank goodness mine has never left my lungs. It is something that you have to learn to deal with. Good luck.
New to this page. Have sarcoid. Any info. on caring for this. Female - cough - shortness of breath. Go to MAYO, but have not been seen for this.
Hi @taurus13 and welcome to Connect. You may have noticed I moved your post to this existing discussion on Sarcoidosis so that you can read what others have said about living with this condition. Simply click VIEW AND REPLY in your email notification in order find your post.
I wanted to introduce you to @martindale, @sarcoidosis, @rod0852 and @riverotter as they have experience with Sarcoidosis and may be able to offer you support.
Back to you @taurus13, how long ago were you diagnosed? Can you share more about your symptoms?
Don't give up. You'll have ups and downs. Take advantage of your ups, read all you can and try to promote healthy things little by little. I tend to want to give up when it flairs up. But you can't. Start slow and try to move ahead a little everyday. Take care.
I use to cough so much, my vocal cords were filled with sores. They wanted to scrape them. After reading about it, I wouldn't let them. I told them I'd teach myself not to cough. I carried water everywhere. I used castor oil packs on my chest. This cleared up the pain and congestion in my chest. I still cough some put not near as much. The shortness of breath is bad on some days. I try to slow down and will stop until I catch my breath. I deal with it because I don't like taking medication. I do take turmeric and it does help. When I stay on a anti inflammatory diet this helps the most. I have oxygen when I do cardio. I was on prednisone for the first 7 years. I hated it. I take a nasal spray for allergies. I am incharge of my health and I must do everything I can to promote it. I fail a lot, but keep on trying. Good luck.
I put castor oil packs on my chest and feet. It relieved me from my pain.
Ai have multisystem sarcoidosis... Must have had it for years. In my spine and bones. In my spleen and liver. I live in Australia.
I will be on an anti inflammatory diet for the rest of my life. Prednisone helps but try to get off it if you can after it has reduced your inflammation...it is not sustainable gives you diabetes,cataracts. Ni meds after low dose prednisone. Pain , yes. I take Tumeric caps. Paracetomol. Yep it does hurt when it gets my joints going. Waxes and wanes. Exercise with regular routine. Martindale, I was first diagnosed by skin and lymph biopsy three years ago. Also in my lungs at that time. PET scan showed the spread and extent of this disease. Please keep in touch.
So sorry you have it so tough. Good luck.
@suscros68 HI there. Has anyone responded to you? I kept this message meaning to respond to you, but somehow the days (and months) slipped by. Just wondering if there is a thread of discussion about this.