Guest guest Posted June 22, 2008 Report Share Posted June 22, 2008 I have a family, but I'm not married. I live with my parents, and I'm on Social Security and Medicaid since before my bone marrow transplant since I cannot work. I have a pulmonary doctor, I've been seeing her on and off since my breathing problems began (I guess it will be a more common dr appt like my oncologist is now), she first diagonsed me with COPD/Asthma. I see her in a couple weeks for a follow up. They have to try and get a atery blood gas since they couldn't get one from me at the hospital for some reason. > > > > > > Hi everybody - I just joined this community this morning. I thought I > > would introduce myself. > > > > My name is , 22 years old, I live in Ohio. I am a T-cell > > Non-hodgkins Lymphoma survivor for 2 years now. I went through > > chemotherapy and also a autologus bone marrow transplant in 2006 (it's > > almost my second birthday for my transplant . Ever since my > > transplant I had trouble breathing, in 2007 I had fluid build up and my > > lungs partially collapsed, so my doctors placed chest tubes to re- expand > > my lungs/drain fluid. Things were going okay until this year (around 8 > > months later) when the shortness of breath came back with a vengence and > > with a sharp chest pain. I was placed on inhalers at first, saying it > > was asthma. But it got to the point where the pain felt like I had a > > semi truck running over my lungs constantly. I had to get a CT scan to > > check for cancer remission and it picked up some fibrosis and partial > > lung collapse (cancer still in remission). This last monday, I was > > following up with the doctor that had placed the chest tubes last year, > > he told me it would be useless to open me up for that. He sent me down > > to the ER due to my shortness of breath and heart rate, I was admitted > > for a week. I found out I had pulmonary fibrosis (it was caused by > > chemotherapy) but there isn't much they can do for me at the moment. > > Steroids wouldn't do a thing just like the tubes wouldn'tve. Got sent > > home with oxygen and new scripts for inhalers and also pain patches, > > they only gave me three this pain is horriable...I'll need more I dunno > > how the dr thinks I can handle it. I didn't get to much into detail, > > there's more but I did the short version. ; > > > Quote Link to comment Share on other sites More sharing options...
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