Pulmonary Sarcoidosis: How are you dealing with it?

Posted by bboxer @bboxer, Dec 25, 2016

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.

My husband has horrible GI and swallowing issues from scarring from the sarcoid. He has one collapsed lobe in his left lung. It is around his heart as well. I never knew what sarcoid was until my husband was diagnosed with it. Our neighbor had it far worse (yep, our neighbor) as it affected so many organ systems for him. He was on prednisone for over a year and needed psychiatric help to deal with it all. And he was way younger than my husband. I am so glad you are able to walk so much. That’s problematic for my husband because breathing is so very hard for him most days. The doctor has discussed his having a lung transplant, but he’s almost 73. Good luck to you! (Irene)

REPLY

Thx for sharing. It’s recently sarcoidosis is affecting my heart and extremely low oxygen level. I’m advised I need to use a oxygen tank. I find keeping my weight down helps, I don’t feel the shortness of breath but hard to do when I’m taking 30 mg prednisone. I’m told to make an appointment at mayo for future Lung transplant, I’m 53 years young!:)

REPLY

I’m not experiencing the pain in or around rib cage but severe shortness of breath which requires me to use an oxygen tank. Prednisone seems to be the only thing that helps in reducing inflammation and lower chance of getting more scare tissue. I believe I had sarcoidosis since 2009 but was diagnosed in September 2015 it’s progressively harder to breathe and I’m waiting for an appointment to qualify for lung transplant.

REPLY
@karmine

Thx for sharing

Jump to this post

The high dosage of prednisone is temporary at 30 mg by the fourth week it will be 5 mg daily, it should be lowered gradually because it’s a steroid . Long term causes diabetes and weight gain

REPLY

I forgot to pass on some more information that was recommended to me for a natural way to help with inflammation. Taking Turmeric and Bromelain daily are supposed to be helpful. I have been taking both for a month or so and can’t really say that I’ve noticed anything. I’m not recommending but you might want to read up on them and decide for yourself. I researched and couldn’t find anything wrong with taking them. Good luck to all and keep the information coming. Rod

REPLY

I've had sarcoid for 30 years I am 50 now it has spreaded to my eyes,skin,bones,heart, kidneys and it started in my liver

REPLY
@kindltmdar1

Hi I wanted to introduce myself. I am a 45 yr old female that has dealt with various autoimmune diseases since I was 15. My current battle is with stage 4 liver cirrhosis and after biopsies on my lungs and liver it was due to sarcoidosis. I have a liver that is full of granulomas. My autoimmune journey started at 15 with Psoriasis, then at 21 after my first child I developed the Psoriatic arthritis to go with it. Then I was diagnosed with Fybro at about 30. The sarcoid started about a year and a half ago when they diagnosed my cirrhosis and that it was not alcohol related. I don't drink. So now I am looking at a transplant list. I have ever specialists imaginable but they all seem not to know how to help me. Starting this month, my feet began to swell and ache. And I mean BAD. at first I thought it was my PA and I was having a flare but after a week and a half of intense pain and ER visits I am exhausted. I just saw my PCP and he is referring me on to more specialists. None of them want to touch me. I also am dealing with acute kidney failure no one seems to understand and on my last MRI they found a mass on my pancreas. Is anyone dealing with this level of extreme autoimmune disease? I am 40% covered with psoriasis and can't walk, on pain meds (which I have never taken regularly even with my history but now have no choice but to take opiates) and don't know where to turn. Is there someone out there that just deals with autoimmune disease? I really don't think in my experience that anyone is looking at someone like me and that all this is related somehow. I have been saying that my whole life. HELP. Thanks for reading.

Jump to this post

Hello @kindltmdar1, welcome to Connect. You certainly have a lot going on and have seen a lot of specialists without any of them coming up with a treatment plan. I’m not sure if it is an option for you but if it is, the Mayo Clinic is very good at diagnosing health issues that are difficult to diagnose. If you would like to seek help from Mayo Clinic, you can contact one of their appointment offices. The contact information for Minnesota, Arizona and Florida can be found here:

Mayo Clinic Contact Information: https://www.mayoclinic.org/appointments

Here is a Mayo Clinic page that provides more information cirrhosis:
-- https://www.mayoclinic.org/diseases-conditions/cirrhosis/diagnosis-treatment/drc-20351492

@kindltmdar1 are you able to have your primary care doctor refer you to Mayo Clinic?

John

REPLY
@kindltmdar1

Hi I wanted to introduce myself. I am a 45 yr old female that has dealt with various autoimmune diseases since I was 15. My current battle is with stage 4 liver cirrhosis and after biopsies on my lungs and liver it was due to sarcoidosis. I have a liver that is full of granulomas. My autoimmune journey started at 15 with Psoriasis, then at 21 after my first child I developed the Psoriatic arthritis to go with it. Then I was diagnosed with Fybro at about 30. The sarcoid started about a year and a half ago when they diagnosed my cirrhosis and that it was not alcohol related. I don't drink. So now I am looking at a transplant list. I have ever specialists imaginable but they all seem not to know how to help me. Starting this month, my feet began to swell and ache. And I mean BAD. at first I thought it was my PA and I was having a flare but after a week and a half of intense pain and ER visits I am exhausted. I just saw my PCP and he is referring me on to more specialists. None of them want to touch me. I also am dealing with acute kidney failure no one seems to understand and on my last MRI they found a mass on my pancreas. Is anyone dealing with this level of extreme autoimmune disease? I am 40% covered with psoriasis and can't walk, on pain meds (which I have never taken regularly even with my history but now have no choice but to take opiates) and don't know where to turn. Is there someone out there that just deals with autoimmune disease? I really don't think in my experience that anyone is looking at someone like me and that all this is related somehow. I have been saying that my whole life. HELP. Thanks for reading.

Jump to this post

@kindtmdar1 Hi! I’m glad that you’re reaching out and looking for answers! You do have many issues going on. If I were you, I would get a second opinion at the least, or if at all possible get to a Mayo Clinic. I say that because they have what they need as a team. What I have experienced so far is they are thorough and get to the bottom of the problem with solutions. Get all the information you can from reliable sources on the internet on your condition to be educated on your conditions. It can get very overwhelming to feel hopeless. I don’t know if your on oxygen for your sarcoidosis or not. Don’t give up whatever you do. You need to stay strong and fight to get better answers. Good Luck in 2019.

REPLY
Please sign in or register to post a reply.