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In April I was diagnosed with an abdominal aortic aneurysm, so i had surgery to place a stent. I was discharged from the hospital the day after surgery, on April 26, on April 27 I started experiencing nausea and lower back pain. By April 29 the nausea was so severe that I couldn't handle drinking anything, which meant I couldn't take my pain pills. This went on all day until I developed a low grade temp, at that point the doctors office said to go straight to the ER. They rain multiple tests to check on the stent. All tests came back clear but they admitted me over night just to keep an eye on me. I went home the following morning with some anti nausea meds, some pain pills and the advice to see me surgeon. I saw my surgeon 2 days later. He felt the lower back pain was from being on his table for so long and would fade and the nausea he felt was my body's way of adjusting to the fact that he cut off blood supply to a portion of my colon during surgery. All of these explanations made sense to me so I didn't pursue it any further. Then i had my 1 month appointment with him and I told him, the lower back pain has faded but something had to be done about the nausea. I explained that I was nauseous all the time, that it was getting worse and that I had not had a cup of coffee since my surgery, it made the nausea worse. At that point it was like a light bulb went off for him when I said that. He asked if I still had my gallbladder. Yes I do. So he said it sounded like it was my gallbladder and he was going to schedule a test, at that point I stopped him, I explained that in order to stop smoking my primary doctor had me on Chantix could that be causing a reaction with the blood thinners? He said no but that since the #1 side effect of Chantix is nausea he wanted me to stop taking it for 2 weeks and then call his office. I did this and the nausea persisted, so I called his office back and explained this so he sent me for an ultra sound. After my ultra sound I was having a hard time getting my surgeons office to let me know the results and since I was starting to experience moderate upper shoulder pain on the right side and pain below my ribs I went ahead and contacted my primary. He accessed the ultra sound results and advised that they came back normal, so he put me on prilosec, ordered blood tests to check my liver and ordered a hida test to check my gallbladder. The prilosec has given me no relief and I just had the blood work and hida done on 7/5. My doctor has only received my blood work which came back normal but the hida results are posted on a medical site that i can access and if I understand it correctly, it's stating that I have an ejection fraction of 15%. Now I'm just waiting on my doctor to give me a call and let me know what my next step is, although from everything I have read, it appears that surgery is in my future. I've noticed that the pain seems to be getting worse but primarily my symptom has been the nausea. I have been nauseous for over 2 months and living on jello, crackers, mashed potatoes and rice. I have no idea how those of you with ejection fractions lower than mine or living with it longer than I have, have done it.
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