Guest guest Posted October 19, 2009 Report Share Posted October 19, 2009 Hi, I had my biopsy the beginning of August at Duke. Dr Noble is my Doctor. I would have sworn that he said that from the biopsy it appeared I did not have IPF but it probably was an autoimmune lung disease. Since the biopsy I was on on oxygen. Though I didn't need it while sitting or sleeping. I'm on all of our favorite drug prednisolone 20 mg plus Cellcept 3g. About a week and a half ago I started getting better to the point where I no longer need oxygen. I'm not saying that I'm 100% better, if I walk at a slightly lower than normal pace I can get maybe 50 yards before I have to rest for a few minutes, my levels then will go down to around 88. The only problem is that at times I forget that I'm not normal and walk along at a brisk pace and my levels quickly plummet to 85-6 or lower. Before I started getting better I didn't bother thinking much about the diagnosis. Doctor Noble said to return in December, if I was getting better I would be there for just a few days, if worse starting the procedures for getting me on the lung transplant path. (I live in Finland) So now that I am getting better I'm wondering about the diagnosis. So here is what Dr Noble put on paper about the biopsy: The pattern was not the typical features of usual interstitial pneumonia. The pattern was more consistent with the fibrosing variant nonspecific interstitial pneumonia, which can be seen in the setting of a connective tissue disease or chronic hypersensitivity pneumonia. Can someone translate that into plain English? Thanks, Mike Dulin Quote Link to comment Share on other sites More sharing options...
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